id rm_id snp_id modification_type species chromosome strand position snp_start snp_end reference_sequence alterative_sequence reference_base alterative_base gene gene_database_id gene_type gene_region modification_sample modification_sample_information sample_peak_id pubmed_id confidence_level rs_id modification_function snp_type snp_database snp_position modification_site tumor sample tissue rbp_id splice_record mirna_id clinvar_record gwas_id circrna_id 55019 RMVar_ID_55019 Human_SNP_ID_659517781 m1A Human chr19 - 15111413 15111413 15111413 GCTGACCAGTGATGACATTGATATCGGGGTACAGGTCCTCAGATAGGCAGACCGCTGCACTGTCC GCTGACCAGTGATGACATTGATATCGGGGTACTGGTCCTCAGATAGGCAGACCGCTGCACTGTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15111363..15111455 26863196 MeRIP-seq:(Medium) rs1161286388 Functional Loss SNV dbSNP153 33..33 33 - - - 55020 RMVar_ID_55020 Human_SNP_ID_659517871 m1A Human chr19 + 15111704 15111704 15111704 CATCACCCAGCCCCTGTATAAGGTGGTACTGGAGGCCATGGCCCGGGACCCCCCAAACAGAGTTC CATCACCCAGCCCCTGTATAAGGTGGTACTGGGGGCCATGGCCCGGGACCCCCCAAACAGAGTTC A G SYDE1 Ensembl:ENSG00000105137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15111654..15111806 26863196 MeRIP-seq:(Medium) rs1332900361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1970210,Human_Splice_Rec_1970211,Human_Splice_Rec_1970226,Human_Splice_Rec_1970227,Human_Splice_Rec_1970234,Human_Splice_Rec_1970235 Human_miRNA_ID_2679055,Human_miRNA_ID_3081095 RMVar_hsa_circ_16438,RMVar_hsa_circ_76187,RMVar_hsa_circ_193081,RMVar_hsa_circ_31917 55021 RMVar_ID_55021 Human_SNP_ID_659518658 m1A Human chr19 - 15114345 15114345 15114345 TGATTTGGTTGGCAGCAGCAAGAGGGCCGACTAGAGGTGACTCACCACACCAGGGTGATGCTCAC TGATTTGGTTGGCAGCAGCAAGAGGGCCGACTTGAGGTGACTCACCACACCAGGGTGATGCTCAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15114247..15114414 26863196 MeRIP-seq:(Medium) rs1348790776 Functional Loss SNV dbSNP153 33..33 33 - - - 55022 RMVar_ID_55022 Human_SNP_ID_659521412 m1A Human chr19 + 15122879 15122879 15122879 GCCCCTCGGCCCCAGCACTGCTCAGCATCACCATCCTCCACCTACCTGGGGTGCCCGACTGGGCG GCCCCTCGGCCCCAGCACTGCTCAGCATCACCTTCCTCCACCTACCTGGGGTGCCCGACTGGGCG A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15122876..15122975 32194978 MeRIP-seq:(Medium) rs773620745 Functional Loss SNV dbSNP153 33..33 33 - - - 55023 RMVar_ID_55023 Human_SNP_ID_659521580 m1A Human chr19 - 15123245 15123245 15123245 AGTGGGCATGGCTGTGATGGGCTCTGTGTTCCAGGGACGGTGGGCGTGGCGGCAGTGACAGCAGG AGTGGGCATGGCTGTGATGGGCTCTGTGTTCCGGGGACGGTGGGCGTGGCGGCAGTGACAGCAGG T C ILVBL Ensembl:ENSG00000105135 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15123121..15123601 32194978 MeRIP-seq:(Medium) rs1266507418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910810,Human_RBP_ID_4506233,Human_RBP_ID_5370085 RMVar_hsa_circ_105656,RMVar_hsa_circ_193085,RMVar_hsa_circ_325442 55024 RMVar_ID_55024 Human_SNP_ID_659521595 m1A Human chr19 - 15123277 15123277 15123277 GGGTTTTTCAGAGGTGGAAGAATGGCCAAGAGAGTGGGCATGGCTGTGATGGGCTCTGTGTTCCA GGGTTTTTCAGAGGTGGAAGAATGGCCAAGAGCGTGGGCATGGCTGTGATGGGCTCTGTGTTCCA T G ILVBL Ensembl:ENSG00000105135 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15123227..15123380 26863196 MeRIP-seq:(Medium) rs1385399234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5370085 RMVar_hsa_circ_105656,RMVar_hsa_circ_193085,RMVar_hsa_circ_325442 55025 RMVar_ID_55025 Human_SNP_ID_659521613 m1A Human chr19 + 15123334 15123331 15123334 AAAAACCCCTACCCTCACAGACACTCTAGCCCACAGTCCAACCAGTCCCCAGCCCTCTCTGCAAT AAAAACCCCTACCCTCACAGACACTCTAGC___CAGTCCAACCAGTCCCCAGCCCTCTCTGCAAT CCCA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15123283..15123382 26863196 MeRIP-seq:(Medium) rs1351307742 Functional Loss DEL dbSNP153 31..33 33 - - - 55026 RMVar_ID_55026 Human_SNP_ID_659521700 m1A Human chr19 - 15123545 15123545 15123545 GGTGGACAAGGCAAGCGTCCGGCATGGCGGAGAGAACGTGGCCGCTGTGCTGAGGGCCCATGGTG GGTGGACAAGGCAAGCGTCCGGCATGGCGGAGGGAACGTGGCCGCTGTGCTGAGGGCCCATGGTG T C ILVBL Ensembl:ENSG00000105135 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15123495..15123582 26863196 MeRIP-seq:(Medium) rs1216458574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239593,Human_RBP_ID_514542,Human_RBP_ID_4557289,Human_RBP_ID_18994489 Human_Splice_Rec_1970266,Human_Splice_Rec_1970294,Human_Splice_Rec_1970380,Human_Splice_Rec_1970394,Human_Splice_Rec_1970404,Human_Splice_Rec_1970416 RMVar_hsa_circ_105656,RMVar_hsa_circ_193085,RMVar_hsa_circ_325442 55027 RMVar_ID_55027 Human_SNP_ID_659522108 m1A Human chr19 + 15125061 15125061 15125061 CAGCGGGGGCGGCGGCCGCGGGGGTCTCCATGAGGTGGTACCTAAGAGAGAAAGGGCACTTCCCA CAGCGGGGGCGGCGGCCGCGGGGGTCTCCATGGGGTGGTACCTAAGAGAGAAAGGGCACTTCCCA A G AC003956.1 Ensembl:ENSG00000268564 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15125012..15125115 26863196 MeRIP-seq:(Medium) rs772215325 Functional Loss SNV dbSNP153 33..33 33 - - - 55028 RMVar_ID_55028 Human_SNP_ID_659522114 m1A Human chr19 - 15125071 15125071 15125071 CGCCCAAGTCTGGGAAGTGCCCTTTCTCTCTTAGGTACCACCTCATGGAGACCCCCGCGGCCGCC CGCCCAAGTCTGGGAAGTGCCCTTTCTCTCTTGGGTACCACCTCATGGAGACCCCCGCGGCCGCC T C ILVBL Ensembl:ENSG00000105135 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15125044..15125132 26863196 MeRIP-seq:(Medium) rs1451512379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557291 Human_Splice_Rec_1970393 55029 RMVar_ID_55029 Human_SNP_ID_659522174 m1A Human chr19 - 15125234 15125234 15125234 ACCTTGTCACGGAGAGGCATGGCTTCACCCCGAGCCTAGGCGCACAAAGGGCGTGGTCTGGCAGG ACCTTGTCACGGAGAGGCATGGCTTCACCCCGCGCCTAGGCGCACAAAGGGCGTGGTCTGGCAGG T G ILVBL Ensembl:ENSG00000105135 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15125229..15125309 26863196 MeRIP-seq:(Medium) rs1484193957 Functional Loss SNV dbSNP153 33..33 33 - - - 55030 RMVar_ID_55030 Human_SNP_ID_659522238 m1A Human chr19 + 15125454 15125454 15125454 CAACCGGACCCCAAATCTCAGCCCCAGTAGTGAGCCCGCCCCATGTTACGTCACCAAGAGGCACG CAACCGGACCCCAAATCTCAGCCCCAGTAGTGCGCCCGCCCCATGTTACGTCACCAAGAGGCACG A C AC003956.1 Ensembl:ENSG00000268564 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15125452..15125704 26863196 MeRIP-seq:(Medium) rs986053720 Functional Loss SNV dbSNP153 33..33 33 - - - 55031 RMVar_ID_55031 Human_SNP_ID_659522242 m1A Human chr19 - 15125467 15125466 15125467 GGGGGCGTGACCTCGTGCCTCTTGGTGACGTAACATGGGGCGGGCTCACTACTGGGGCTGAGATT GGGGGCGTGACCTCGTGCCTCTTGGTGACGTA_CATGGGGCGGGCTCACTACTGGGGCTGAGATT GT G ILVBL Ensembl:ENSG00000105135 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15125459..15125608 32194978 MeRIP-seq:(Medium) rs1333613187 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6723095,Human_RBP_ID_17916031 Human_Splice_Rec_1970361,Human_Splice_Rec_1970413 55032 RMVar_ID_55032 Human_SNP_ID_659522247 m1A Human chr19 + 15125487 15125487 15125487 GCCCGCCCCATGTTACGTCACCAAGAGGCACGAGGTCACGCCCCCGGGTTAGCGGGCGCGACCCT GCCCGCCCCATGTTACGTCACCAAGAGGCACGGGGTCACGCCCCCGGGTTAGCGGGCGCGACCCT A G AC003956.1 Ensembl:ENSG00000268564 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr19:15125474..15125607;chr19:15125486..15125745 26863196 MeRIP-seq:(Medium) rs1429485380 Functional Loss SNV dbSNP153 33..33 33 - - - 55033 RMVar_ID_55033 Human_SNP_ID_659531144 m1A Human chr19 + 15161133 15161133 15161133 GGCAGCCGGGCCCAATCGAGGGGCACAGCCACAGGGTTCAGCAGGCCCAGGCTGAGTACACATCC GGCAGCCGGGCCCAATCGAGGGGCACAGCCACGGGGTTCAGCAGGCCCAGGCTGAGTACACATCC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15161085..15161286 32194978 MeRIP-seq:(Medium) rs1420902596 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 55034 RMVar_ID_55034 Human_SNP_ID_659532632 m1A Human chr19 + 15165928 15165928 15165928 TCAGCACGGGCATAACGGGCAGCCAGGTGCAAAGCAGTCTCGCCAGTACGGTCAGTCCGTGCCCC TCAGCACGGGCATAACGGGCAGCCAGGTGCAAGGCAGTCTCGCCAGTACGGTCAGTCCGTGCCCC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15165879..15166080 32194978 MeRIP-seq:(Medium) rs16980398 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_143 55035 RMVar_ID_55035 Human_SNP_ID_659536647 m1A Human chr19 - 15177615 15177615 15177615 ATGCGAGGCGCTGCAGTGCTGGCGCCTCTTCAACAACAGCCGCTGCGACCCCGCCTGCAGCTCGC ATGCGAGGCGCTGCAGTGCTGGCGCCTCTTCAGCAACAGCCGCTGCGACCCCGCCTGCAGCTCGC T C NOTCH3 Ensembl:ENSG00000074181 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:15177526..15177650 26863410 MeRIP-seq:(Medium) rs761506399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1970473 RMVar_hsa_circ_111070,RMVar_hsa_circ_193094,RMVar_hsa_circ_108034,RMVar_hsa_circ_113686,RMVar_hsa_circ_104390,RMVar_hsa_circ_193096,RMVar_hsa_circ_193095,RMVar_hsa_circ_115610,RMVar_hsa_circ_193101,RMVar_hsa_circ_119204,RMVar_hsa_circ_193102,RMVar_hsa_circ_193103 55036 RMVar_ID_55036 Human_SNP_ID_659539121 m1A Human chr19 - 15185278 15185278 15185278 CATGCAGCAGCGATGGAATGGGTTTCCACTGCACCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC CATGCAGCAGCGATGGAATGGGTTTCCACTGCTCCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC T A NOTCH3 Ensembl:ENSG00000074181 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15184992..15185508 32194978 MeRIP-seq:(Medium) rs1442324683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514609 Human_Splice_Rec_1970453,Human_Splice_Rec_1970529 RMVar_hsa_circ_109200,RMVar_hsa_circ_111070,RMVar_hsa_circ_193094,RMVar_hsa_circ_108034,RMVar_hsa_circ_104390,RMVar_hsa_circ_193095,RMVar_hsa_circ_115610,RMVar_hsa_circ_193101,RMVar_hsa_circ_105182,RMVar_hsa_circ_193103,RMVar_hsa_circ_193106,RMVar_hsa_circ_266410,RMVar_hsa_circ_4986,RMVar_hsa_circ_94590,RMVar_hsa_circ_112719,RMVar_hsa_circ_193110,RMVar_hsa_circ_193111,RMVar_hsa_circ_324145,RMVar_hsa_circ_76833,RMVar_hsa_circ_4681,RMVar_hsa_circ_111564,RMVar_hsa_circ_193112,RMVar_hsa_circ_193113,RMVar_hsa_circ_38746,RMVar_hsa_circ_82699,RMVar_hsa_circ_193114,RMVar_hsa_circ_193115 55037 RMVar_ID_55037 Human_SNP_ID_659539122 m1A Human chr19 - 15185278 15185278 15185278 CATGCAGCAGCGATGGAATGGGTTTCCACTGCACCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC CATGCAGCAGCGATGGAATGGGTTTCCACTGCCCCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC T G NOTCH3 Ensembl:ENSG00000074181 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15184992..15185508 32194978 MeRIP-seq:(Medium) rs1442324683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514609 Human_Splice_Rec_1970453,Human_Splice_Rec_1970529 RMVar_hsa_circ_109200,RMVar_hsa_circ_111070,RMVar_hsa_circ_193094,RMVar_hsa_circ_108034,RMVar_hsa_circ_104390,RMVar_hsa_circ_193095,RMVar_hsa_circ_115610,RMVar_hsa_circ_193101,RMVar_hsa_circ_105182,RMVar_hsa_circ_193103,RMVar_hsa_circ_193106,RMVar_hsa_circ_266410,RMVar_hsa_circ_4986,RMVar_hsa_circ_94590,RMVar_hsa_circ_112719,RMVar_hsa_circ_193110,RMVar_hsa_circ_193111,RMVar_hsa_circ_324145,RMVar_hsa_circ_76833,RMVar_hsa_circ_4681,RMVar_hsa_circ_111564,RMVar_hsa_circ_193112,RMVar_hsa_circ_193113,RMVar_hsa_circ_38746,RMVar_hsa_circ_82699,RMVar_hsa_circ_193114,RMVar_hsa_circ_193115 55038 RMVar_ID_55038 Human_SNP_ID_659543899 m1A Human chr19 - 15200939 15200933 15200940 GGCTGGCCCGGGACGCGCCCGGAGCCCAGGGAAGGAGGGAGGAGGGGAGGGTCGCGGCCGGCCGC GGCTGGCCCGGGACGCGCCCGGAGCCCAGGG_______GAGGAGGGGAGGGTCGCGGCCGGCCGC CCCTCCTT C NOTCH3 Ensembl:ENSG00000074181 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:15200839..15200973 26863410 MeRIP-seq:(Medium) rs1296128498 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_4506321 RMVar_hsa_circ_95055,RMVar_hsa_circ_193118 55039 RMVar_ID_55039 Human_SNP_ID_659554875 m1A Human chr19 - 15237925 15237925 15237925 TCCCCACACCCCAGCCATCGCCGCCCGCTCCCAGGAGGCCAGGGCAGGCCTGCGTGGGCTGGAGG TCCCCACACCCCAGCCATCGCCGCCCGCTCCCGGGAGGCCAGGGCAGGCCTGCGTGGGCTGGAGG T C BRD4 Ensembl:ENSG00000141867 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:15237877..15238011;chr19:15237876..15238037 26863196 MeRIP-seq:(Medium) rs567892805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241649,Human_RBP_ID_1067480,Human_RBP_ID_1093697,Human_RBP_ID_4506359,Human_RBP_ID_6723194,Human_RBP_ID_9328722,Human_RBP_ID_26473651 Human_miRNA_ID_254334 55040 RMVar_ID_55040 Human_SNP_ID_659555772 m1A Human chr19 - 15239970 15239970 15239970 TCCCCGCTTATGATACATTCCCCCCAGATGTCACAGTTCCAGAGCCTGACCCACCAGTCTCCACC TCCCCGCTTATGATACATTCCCCCCAGATGTCCCAGTTCCAGAGCCTGACCCACCAGTCTCCACC T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:15238802..15243102;chr19:15239701..15243069 26863196 MeRIP-seq:(Medium) rs144097229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54191,Human_RBP_ID_5130291,Human_RBP_ID_13378834,Human_RBP_ID_17082349,Human_RBP_ID_17266869,Human_RBP_ID_17386706,Human_RBP_ID_17502420,Human_RBP_ID_18723540,Human_RBP_ID_18946625,Human_RBP_ID_24375538,Human_RBP_ID_26465251,Human_RBP_ID_27464372 Human_Splice_Rec_1970630,Human_Splice_Rec_1970631 Human_miRNA_ID_881257,Human_miRNA_ID_955825,Human_miRNA_ID_2722718,Human_miRNA_ID_3070123 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55041 RMVar_ID_55041 Human_SNP_ID_659555798 m1A Human chr19 - 15240019 15240019 15240019 CTTGACACATTCCTTGTCCCTTCTCCTAGGTCACCTCCGCGAAGCCCCCTCCCCGCTTATGATAC CTTGACACATTCCTTGTCCCTTCTCCTAGGTCGCCTCCGCGAAGCCCCCTCCCCGCTTATGATAC T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:15239992..15242969 26863196 MeRIP-seq:(Medium) rs1026979615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130292,Human_RBP_ID_17083023,Human_RBP_ID_17272378,Human_RBP_ID_17386707,Human_RBP_ID_17497996,Human_RBP_ID_17656856,Human_RBP_ID_18945160 Human_Splice_Rec_1970630 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55042 RMVar_ID_55042 Human_SNP_ID_659556708 m1A Human chr19 - 15242921 15242921 15242921 TCATCCAGCACCACCATTCACCCCGGCACCACAAGTCGGACCCCTACTCAACCGGTAAGTGGTCC TCATCCAGCACCACCATTCACCCCGGCACCACGAGTCGGACCCCTACTCAACCGGTAAGTGGTCC T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15239383..15244625 26863196 MeRIP-seq:(Medium) rs1442261328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130293,Human_RBP_ID_9293480,Human_RBP_ID_17083024,Human_RBP_ID_17266870,Human_RBP_ID_17382247,Human_RBP_ID_17497997,Human_RBP_ID_18946626,Human_RBP_ID_27464373 Human_Splice_Rec_1970629 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55043 RMVar_ID_55043 Human_SNP_ID_659556740 m1A Human chr19 - 15242985 15242985 15242985 CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCACCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCGCCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr19:15242976..15243184;chr19:15242860..15243000 26863196 MeRIP-seq:(Medium) rs930035134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514693,Human_RBP_ID_5130294,Human_RBP_ID_17082350,Human_RBP_ID_17271784,Human_RBP_ID_17386710,Human_RBP_ID_17502601,Human_RBP_ID_17656857,Human_RBP_ID_18945161 Human_Splice_Rec_1970629 Human_miRNA_ID_2147363,Human_miRNA_ID_2988789,Human_miRNA_ID_3022490 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55044 RMVar_ID_55044 Human_SNP_ID_659556741 m1A Human chr19 - 15242985 15242985 15242985 CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCACCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCCCCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr19:15242976..15243184;chr19:15242860..15243000 26863196 MeRIP-seq:(Medium) rs930035134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514693,Human_RBP_ID_5130294,Human_RBP_ID_17082350,Human_RBP_ID_17271784,Human_RBP_ID_17386710,Human_RBP_ID_17502601,Human_RBP_ID_17656857,Human_RBP_ID_18945161 Human_Splice_Rec_1970629 Human_miRNA_ID_2147363,Human_miRNA_ID_2988789,Human_miRNA_ID_3022490 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55045 RMVar_ID_55045 Human_SNP_ID_659556979 m1A Human chr19 - 15243348 15243348 15243348 ACACCCCTGCTCCCACAGCCCCCCATGGCCCAACCCCCCCAAGTGCTGCTGGAGGATGAAGAGCC ACACCCCTGCTCCCACAGCCCCCCATGGCCCAGCCCCCCCAAGTGCTGCTGGAGGATGAAGAGCC T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:15242998..15243500 26863196 MeRIP-seq:(Medium) rs1252813939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54195,Human_RBP_ID_771774,Human_RBP_ID_1067481,Human_RBP_ID_5130298,Human_RBP_ID_5321488,Human_RBP_ID_9293481,Human_RBP_ID_17081742,Human_RBP_ID_17386712,Human_RBP_ID_17656858,Human_RBP_ID_17916063,Human_RBP_ID_18945164 Human_miRNA_ID_2102386,Human_miRNA_ID_2108340,Human_miRNA_ID_2114280,Human_miRNA_ID_2166826,Human_miRNA_ID_2479718,Human_miRNA_ID_2598083,Human_miRNA_ID_2740989,Human_miRNA_ID_3041576 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55046 RMVar_ID_55046 Human_SNP_ID_659557466 m1A Human chr19 + 15244592 15244589 15244592 GCCGGGGCCTGCTGCATCTGCTGATGGTGGTGATGATGGTGCTGCAGACAGAGAGACAGACAGAC GCCGGGGCCTGCTGCATCTGCTGATGGTGG___TGATGGTGCTGCAGACAGAGAGACAGACAGAC GTGA G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15244311..15244612 32194978 MeRIP-seq:(Medium) rs774637350 Functional Loss DEL dbSNP153 31..33 33 - - - 55047 RMVar_ID_55047 Human_SNP_ID_659557467 m1A Human chr19 + 15244592 15244592 15244592 GCCGGGGCCTGCTGCATCTGCTGATGGTGGTGATGATGGTGCTGCAGACAGAGAGACAGACAGAC GCCGGGGCCTGCTGCATCTGCTGATGGTGGTGGTGATGGTGCTGCAGACAGAGAGACAGACAGAC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15244311..15244612 32194978 MeRIP-seq:(Medium) rs199890542 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 55048 RMVar_ID_55048 Human_SNP_ID_659558401 m1A Human chr19 + 15247217 15247217 15247217 CCCCAGCCCCACTCCAGTGAAGGAGGTAATGGAGGGTAAGGTCAGGGCAGAGGAGAGGAGTCCCC CCCCAGCCCCACTCCAGTGAAGGAGGTAATGGTGGGTAAGGTCAGGGCAGAGGAGAGGAGTCCCC A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15247197..15247348 32194978 MeRIP-seq:(Medium) rs574873060 Functional Loss SNV dbSNP153 33..33 33 - - - 55049 RMVar_ID_55049 Human_SNP_ID_659558525 m1A Human chr19 - 15247563 15247563 15247563 GCATGCTGCCCCCGACACACGCACGCACGCGCACACACGTGTGCACATGGGCCATAGCCACAAGC GCATGCTGCCCCCGACACACGCACGCACGCGCGCACACGTGTGCACATGGGCCATAGCCACAAGC T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15247547..15247898 32194978 MeRIP-seq:(Medium) rs1327124969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514704,Human_RBP_ID_13379007 Human_miRNA_ID_322729,Human_miRNA_ID_325510 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55050 RMVar_ID_55050 Human_SNP_ID_659560551 m1A Human chr19 - 15253709 15253709 15253709 CGTATCACAGTCACGTGCAGTGCGGCCGCTTCAGGGAGATGCTTCGCTGGTTTCTGGTGGATGTG CGTATCACAGTCACGTGCAGTGCGGCCGCTTCGGGGAGATGCTTCGCTGGTTTCTGGTGGATGTG T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15253697..15253847 32194978 MeRIP-seq:(Medium) rs760034397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1970684 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 55051 RMVar_ID_55051 Human_SNP_ID_659561248 m1A Human chr19 - 15255588 15255588 15255588 TGATGGTGTCTGCATCGTCCCTTCGTAGCAAGAAGGAGCCAGCGCCCATGAAGAGCAAGCCCCCT TGATGGTGTCTGCATCGTCCCTTCGTAGCAAGGAGGAGCCAGCGCCCATGAAGAGCAAGCCCCCT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15255344..15255622 26863196 MeRIP-seq:(Medium) rs201628843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54212,Human_RBP_ID_908507,Human_RBP_ID_8839856,Human_RBP_ID_9258987,Human_RBP_ID_9380699,Human_RBP_ID_17502606,Human_RBP_ID_18412307,Human_RBP_ID_24545454,Human_RBP_ID_26334884,Human_RBP_ID_26984143,Human_RBP_ID_27815236 Human_Splice_Rec_1970620,Human_Splice_Rec_1970658,Human_Splice_Rec_1970680 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 55052 RMVar_ID_55052 Human_SNP_ID_659561452 m1A Human chr19 - 15256168 15256168 15256168 AAGGAGAAAGACAAGAAGGAAAAGAAAAAAGAAAAGCACAAAAGGAAAGAGGAAGTGGAAGAGAA AAGGAGAAAGACAAGAAGGAAAAGAAAAAAGAGAAGCACAAAAGGAAAGAGGAAGTGGAAGAGAA T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15256051..15256250 26863196 MeRIP-seq:(Medium) rs1205696471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2557553,Human_RBP_ID_22967396,Human_RBP_ID_24545583 Human_Splice_Rec_1970618,Human_Splice_Rec_1970656,Human_Splice_Rec_1970678,Human_Splice_Rec_1970702,Human_Splice_Rec_1970708,Human_Splice_Rec_1970710 Human_miRNA_ID_2237763 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 55053 RMVar_ID_55053 Human_SNP_ID_659561453 m1A Human chr19 - 15256171 15256171 15256171 AAAAAGGAGAAAGACAAGAAGGAAAAGAAAAAAGAAAAGCACAAAAGGAAAGAGGAAGTGGAAGA AAAAAGGAGAAAGACAAGAAGGAAAAGAAAAAGGAAAAGCACAAAAGGAAAGAGGAAGTGGAAGA T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15256051..15256225 26863196 MeRIP-seq:(Medium) rs149289085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2557553,Human_RBP_ID_22809618,Human_RBP_ID_24545583 Human_Splice_Rec_1970618,Human_Splice_Rec_1970656,Human_Splice_Rec_1970678,Human_Splice_Rec_1970702,Human_Splice_Rec_1970708,Human_Splice_Rec_1970710 Human_miRNA_ID_2237763 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 55054 RMVar_ID_55054 Human_SNP_ID_659561455 m1A Human chr19 - 15256176 15256176 15256176 CAAAGAAAAAGGAGAAAGACAAGAAGGAAAAGAAAAAAGAAAAGCACAAAAGGAAAGAGGAAGTG CAAAGAAAAAGGAGAAAGACAAGAAGGAAAAGCAAAAAGAAAAGCACAAAAGGAAAGAGGAAGTG T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15256048..15256275 26863196 MeRIP-seq:(Medium) rs905328756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2557553,Human_RBP_ID_22809618,Human_RBP_ID_24545583 Human_Splice_Rec_1970618,Human_Splice_Rec_1970656,Human_Splice_Rec_1970678,Human_Splice_Rec_1970702,Human_Splice_Rec_1970708,Human_Splice_Rec_1970710 Human_miRNA_ID_2237763 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 55055 RMVar_ID_55055 Human_SNP_ID_659564105 m1A Human chr19 - 15264702 15264702 15264702 CACCACCCCCACCACCATTGACCCCATTCACGAGCCACCCTCGCTGCCCCCGGAGCCCAAGACCA CACCACCCCCACCACCATTGACCCCATTCACGGGCCACCCTCGCTGCCCCCGGAGCCCAAGACCA T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15264676..15264725 26863196 MeRIP-seq:(Medium) rs777321164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54216,Human_RBP_ID_8830072,Human_RBP_ID_9293489,Human_RBP_ID_13379653,Human_RBP_ID_18723600,Human_RBP_ID_26335908,Human_RBP_ID_27816226 Human_Splice_Rec_1970612,Human_Splice_Rec_1970650,Human_Splice_Rec_1970672,Human_Splice_Rec_1970696 RMVar_hsa_circ_107707,RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55056 RMVar_ID_55056 Human_SNP_ID_659564128 m1A Human chr19 - 15264740 15264740 15264740 TGGCAGACAAAGAAGGGAGTGAAGAGGAAAGCAGACACCACCACCCCCACCACCATTGACCCCAT TGGCAGACAAAGAAGGGAGTGAAGAGGAAAGCGGACACCACCACCCCCACCACCATTGACCCCAT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:15264639..15264824 26863196 MeRIP-seq:(Medium) rs1387038446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54216,Human_RBP_ID_910823,Human_RBP_ID_1067483,Human_RBP_ID_9382157,Human_RBP_ID_27816227 Human_Splice_Rec_1970612,Human_Splice_Rec_1970650,Human_Splice_Rec_1970672,Human_Splice_Rec_1970696 RMVar_hsa_circ_107707,RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55057 RMVar_ID_55057 Human_SNP_ID_659564319 m1A Human chr19 - 15265391 15265391 15265391 ACCCGCTCCAGCTCCCCAGCCCGTACAGAGCCACCCACCCATCATCGCGGCCACCCCACAGCCTG ACCCGCTCCAGCTCCCCAGCCCGTACAGAGCCGCCCACCCATCATCGCGGCCACCCCACAGCCTG T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:15265351..15265600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_54217,Human_RBP_ID_9382158,Human_RBP_ID_17082359,Human_RBP_ID_17266896,Human_RBP_ID_17386720,Human_RBP_ID_17502607,Human_RBP_ID_18945168,Human_RBP_ID_19089506,Human_RBP_ID_27464407 Human_Splice_Rec_1970611,Human_Splice_Rec_1970649,Human_Splice_Rec_1970671,Human_Splice_Rec_1970695 Human_miRNA_ID_3070124 RMVar_hsa_circ_107707,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55058 RMVar_ID_55058 Human_SNP_ID_659564320 m1A Human chr19 - 15265391 15265391 15265391 ACCCGCTCCAGCTCCCCAGCCCGTACAGAGCCACCCACCCATCATCGCGGCCACCCCACAGCCTG ACCCGCTCCAGCTCCCCAGCCCGTACAGAGCCCCCCACCCATCATCGCGGCCACCCCACAGCCTG T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:15265351..15265600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_54217,Human_RBP_ID_9382158,Human_RBP_ID_17082359,Human_RBP_ID_17266896,Human_RBP_ID_17386720,Human_RBP_ID_17502607,Human_RBP_ID_18945168,Human_RBP_ID_19089506,Human_RBP_ID_27464407 Human_Splice_Rec_1970611,Human_Splice_Rec_1970649,Human_Splice_Rec_1970671,Human_Splice_Rec_1970695 Human_miRNA_ID_3070124 RMVar_hsa_circ_107707,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55059 RMVar_ID_55059 Human_SNP_ID_659564376 m1A Human chr19 + 15265474 15265474 15265474 GGCACTGGCGGGGGCGTCTGCAGTGGCTGGGGAGGCACCACTGTCATGACAGGGGTCTGGACGAT GGCACTGGCGGGGGCGTCTGCAGTGGCTGGGGGGGCACCACTGTCATGACAGGGGTCTGGACGAT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15264564..15267475 26863196 MeRIP-seq:(Medium) rs113935053 Functional Loss SNV dbSNP153 33..33 33 - - - 55060 RMVar_ID_55060 Human_SNP_ID_659564377 m1A Human chr19 + 15265474 15265474 15265474 GGCACTGGCGGGGGCGTCTGCAGTGGCTGGGGAGGCACCACTGTCATGACAGGGGTCTGGACGAT GGCACTGGCGGGGGCGTCTGCAGTGGCTGGGGTGGCACCACTGTCATGACAGGGGTCTGGACGAT A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15264564..15267475 26863196 MeRIP-seq:(Medium) rs113935053 Functional Loss SNV dbSNP153 33..33 33 - - - 55061 RMVar_ID_55061 Human_SNP_ID_659564415 m1A Human chr19 - 15265542 15265542 15265542 CCCCTCAGCCGAATCCTCCTCCTGTGCAGGCCACGCCTCACCCCTTCCCTGCCGTCACCCCGGAC CCCCTCAGCCGAATCCTCCTCCTGTGCAGGCCGCGCCTCACCCCTTCCCTGCCGTCACCCCGGAC T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:15265444..15265600 26863410 MeRIP-seq:(Medium) rs1424285081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54218,Human_RBP_ID_240370,Human_RBP_ID_514729,Human_RBP_ID_4563006,Human_RBP_ID_5130302,Human_RBP_ID_6723395,Human_RBP_ID_13379659,Human_RBP_ID_17272382,Human_RBP_ID_17386722,Human_RBP_ID_18945169,Human_RBP_ID_22533125,Human_RBP_ID_26337610 Human_miRNA_ID_2385839 RMVar_hsa_circ_107707,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55062 RMVar_ID_55062 Human_SNP_ID_659564416 m1A Human chr19 - 15265542 15265542 15265542 CCCCTCAGCCGAATCCTCCTCCTGTGCAGGCCACGCCTCACCCCTTCCCTGCCGTCACCCCGGAC CCCCTCAGCCGAATCCTCCTCCTGTGCAGGCCCCGCCTCACCCCTTCCCTGCCGTCACCCCGGAC T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:15265444..15265600 26863410 MeRIP-seq:(Medium) rs1424285081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54218,Human_RBP_ID_240370,Human_RBP_ID_514729,Human_RBP_ID_4563006,Human_RBP_ID_5130302,Human_RBP_ID_6723395,Human_RBP_ID_13379659,Human_RBP_ID_17272382,Human_RBP_ID_17386722,Human_RBP_ID_18945169,Human_RBP_ID_22533125,Human_RBP_ID_26337610 Human_miRNA_ID_2385839 RMVar_hsa_circ_107707,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55063 RMVar_ID_55063 Human_SNP_ID_659564426 m1A Human chr19 - 15265562 15265562 15265562 GACTCCTCCGCAGACCCAGACCCCTCAGCCGAATCCTCCTCCTGTGCAGGCCACGCCTCACCCCT GACTCCTCCGCAGACCCAGACCCCTCAGCCGAGTCCTCCTCCTGTGCAGGCCACGCCTCACCCCT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:15264726..15265650 26863196 MeRIP-seq:(Medium) rs1463048570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54218,Human_RBP_ID_5130302,Human_RBP_ID_17272382,Human_RBP_ID_17386722,Human_RBP_ID_18945169,Human_RBP_ID_26337610 Human_Splice_Rec_1970610,Human_Splice_Rec_1970648,Human_Splice_Rec_1970670,Human_Splice_Rec_1970694,Human_Splice_Rec_1970720 RMVar_hsa_circ_107707,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 55064 RMVar_ID_55064 Human_SNP_ID_659566347 m1A Human chr19 - 15272973 15272973 15272973 AGGCCCAACCCCAGCCAGCCAACGCAGCCAGCACCAACCCCCCGCCCCCAGAGACCTCCAACCCT AGGCCCAACCCCAGCCAGCCAACGCAGCCAGCGCCAACCCCCCGCCCCCAGAGACCTCCAACCCT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:15272926..15273025 26863196 MeRIP-seq:(Medium) rs201234217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54224,Human_RBP_ID_26465294,Human_RBP_ID_26984180,Human_RBP_ID_27269068,Human_RBP_ID_27816231 Human_miRNA_ID_2147367,Human_miRNA_ID_2387387,Human_miRNA_ID_2388860,Human_miRNA_ID_2435275,Human_miRNA_ID_2988793,Human_miRNA_ID_3022494,Human_miRNA_ID_3031068 RMVar_hsa_circ_352477,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297,RMVar_hsa_circ_300690,RMVar_hsa_circ_193129,RMVar_hsa_circ_193128,RMVar_hsa_circ_278323,RMVar_hsa_circ_292398 55065 RMVar_ID_55065 Human_SNP_ID_659566398 m1A Human chr19 + 15273112 15273112 15273112 GGGCCGCTCTCCGCAGACATGCTAGTGATCCCATCACATTCTTCACCAGGCACTCTACAAAGGAA GGGCCGCTCTCCGCAGACATGCTAGTGATCCCGTCACATTCTTCACCAGGCACTCTACAAAGGAA A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15272826..15275705 26863196 MeRIP-seq:(Medium) rs1231437382 Functional Loss SNV dbSNP153 33..33 33 - - - 55066 RMVar_ID_55066 Human_SNP_ID_659584438 m1A Human chr19 + 15331992 15331979 15331992 CCGCCGGCCCCGCCGCGGCGCCCGCGCCCCCCACCCGCGCCCCGCCGGCCAGCCCAAGCCCGGGT CCGCCGGCCCCGCCGCGGCG_____________CCCGCGCCCCGCCGGCCAGCCCAAGCCCGGGT GCCCGCGCCCCCCA G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15331986..15332092 26863196 MeRIP-seq:(Medium) rs1190967086 Functional Loss DEL dbSNP153 21..33 33 - - - 55067 RMVar_ID_55067 Human_SNP_ID_659584448 m1A Human chr19 + 15331992 15331992 15331992 CCGCCGGCCCCGCCGCGGCGCCCGCGCCCCCCACCCGCGCCCCGCCGGCCAGCCCAAGCCCGGGT CCGCCGGCCCCGCCGCGGCGCCCGCGCCCCCCCCCCGCGCCCCGCCGGCCAGCCCAAGCCCGGGT A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15331986..15332092 26863196 MeRIP-seq:(Medium) rs1299529567 Functional Loss SNV dbSNP153 33..33 33 - - - 55068 RMVar_ID_55068 Human_SNP_ID_659590943 m1A Human chr19 - 15355260 15355260 15355260 GAGACACCTGAGGAGGTGGCCGCGGACGTCTTAGCAGAGGTGATTACAGCAGCAGTGAGGGCCGT GAGACACCTGAGGAGGTGGCCGCGGACGTCTTGGCAGAGGTGATTACAGCAGCAGTGAGGGCCGT T C AKAP8 Ensembl:ENSG00000105127 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15355151..15355325 26863196 MeRIP-seq:(Medium) rs1487920651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526883,Human_RBP_ID_6723900,Human_RBP_ID_13382039,Human_RBP_ID_26335914 55069 RMVar_ID_55069 Human_SNP_ID_659590948 m1A Human chr19 - 15355267 15355267 15355267 TAAGAAAGAGACACCTGAGGAGGTGGCCGCGGACGTCTTAGCAGAGGTGATTACAGCAGCAGTGA TAAGAAAGAGACACCTGAGGAGGTGGCCGCGGTCGTCTTAGCAGAGGTGATTACAGCAGCAGTGA T A AKAP8 Ensembl:ENSG00000105127 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15355097..15355333 26863196 MeRIP-seq:(Medium) rs1394013997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526883,Human_RBP_ID_6723900,Human_RBP_ID_13382039,Human_RBP_ID_26335914 55070 RMVar_ID_55070 Human_SNP_ID_659596860 m1A Human chr19 + 15372867 15372867 15372867 CCTTGCGAGGGCTTACCCGATCCCGATCCCGCATCCGAGGCTGCGAGCGGCCACATCCGTAGGGC CCTTGCGAGGGCTTACCCGATCCCGATCCCGCGTCCGAGGCTGCGAGCGGCCACATCCGTAGGGC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15372839..15373037 26863196 MeRIP-seq:(Medium) rs1265500562 Functional Loss SNV dbSNP153 33..33 33 - - - 55071 RMVar_ID_55071 Human_SNP_ID_659597013 m1A Human chr19 + 15373098 15373098 15373098 ACGCAGCGGGGGGCACGAAGGGGTCGCTGCGCATGAAGGTGCCAGGGTTGCTCCGGTCCTGGAAG ACGCAGCGGGGGGCACGAAGGGGTCGCTGCGCGTGAAGGTGCCAGGGTTGCTCCGGTCCTGGAAG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:15373001..15373165 26863410 MeRIP-seq:(Medium) rs1403417073 Functional Loss SNV dbSNP153 33..33 33 - - - 55072 RMVar_ID_55072 Human_SNP_ID_659597432 m1A Human chr19 - 15374035 15374035 15374035 AGGTTATGAAAACTACAATTACTATGGCGCCCAGAACACCAGTGTCACCACAGGCGCAACCTACA AGGTTATGAAAACTACAATTACTATGGCGCCCGGAACACCAGTGTCACCACAGGCGCAACCTACA T C AKAP8 Ensembl:ENSG00000105127 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15373906..15379047 26863196 MeRIP-seq:(Medium) rs1211065572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907455,Human_RBP_ID_9380716,Human_RBP_ID_17916160,Human_RBP_ID_26817159 Human_Splice_Rec_1970744,Human_Splice_Rec_1970816 RMVar_hsa_circ_33045,RMVar_hsa_circ_267662,RMVar_hsa_circ_51564,RMVar_hsa_circ_266554 55073 RMVar_ID_55073 Human_SNP_ID_659599224 m1A Human chr19 + 15379422 15379422 15379422 CGGAAGGACTCCGCCGAAGGTGAGGGGCAAAAACGGCCCACACTGTCTAAGACGCCCCCACGAAG CGGAAGGACTCCGCCGAAGGTGAGGGGCAAAACCGGCCCACACTGTCTAAGACGCCCCCACGAAG A C AC005785.1 Ensembl:ENSG00000268189 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15379418..15379800 26863196 MeRIP-seq:(Medium) rs1247733049 Functional Loss SNV dbSNP153 33..33 33 - - - 55074 RMVar_ID_55074 Human_SNP_ID_659599334 m1A Human chr19 + 15379668 15379668 15379668 GCGGCAGTCTGCGCAGCGGCTGCGTCGCCCGCACAGAGCCTTCCCTCCCCGCTCCGCACCCAGCA GCGGCAGTCTGCGCAGCGGCTGCGTCGCCCGCCCAGAGCCTTCCCTCCCCGCTCCGCACCCAGCA A C AC005785.1 Ensembl:ENSG00000268189 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15379660..15379775 26863196 MeRIP-seq:(Medium) rs1002471893 Functional Loss SNV dbSNP153 33..33 33 - - - 55075 RMVar_ID_55075 Human_SNP_ID_659599404 m1A Human chr19 - 15379761 15379761 15379761 CTGAACGCATGCGTGCTGTGGTCGCCTAGTAAACGGGGCTGCTGGTGGGCCGCGTCGAAGACATG CTGAACGCATGCGTGCTGTGGTCGCCTAGTAAGCGGGGCTGCTGGTGGGCCGCGTCGAAGACATG T C AKAP8 Ensembl:ENSG00000105127 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:15379684..15379811;chr19:15379660..15379800 26863196 MeRIP-seq:(Medium) rs954066857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420873 Human_Splice_Rec_1970739,Human_Splice_Rec_1970785,Human_Splice_Rec_1970799 55076 RMVar_ID_55076 Human_SNP_ID_659599749 m1A Human chr19 - 15380342 15380342 15380342 GGGCGGTGCCCTGGACGAGGGGGCGCAGGGCGAAGCGGCAGGGATCTCGGAGGGCGCAGAGGGCG GGGCGGTGCCCTGGACGAGGGGGCGCAGGGCGGAGCGGCAGGGATCTCGGAGGGCGCAGAGGGCG T C AKAP8L Ensembl:ENSG00000011243 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:15380296..15380398 32194978 MeRIP-seq:(Medium) rs1488925397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241029,Human_RBP_ID_263846,Human_RBP_ID_5116764,Human_RBP_ID_18994499,Human_RBP_ID_22446526,Human_RBP_ID_26335920 Human_Splice_Rec_1970842,Human_Splice_Rec_1970870,Human_Splice_Rec_1970894,Human_Splice_Rec_1970922,Human_Splice_Rec_1970946 RMVar_hsa_circ_265663 55077 RMVar_ID_55077 Human_SNP_ID_659599784 m1A Human chr19 - 15380387 15380387 15380387 TTTCACCGACAGCCCCGAGGAGGAGAAGGAGCAGGAGGAGGCTGAGGGCGGTGCCCTGGACGAGG TTTCACCGACAGCCCCGAGGAGGAGAAGGAGCCGGAGGAGGCTGAGGGCGGTGCCCTGGACGAGG T G AKAP8L Ensembl:ENSG00000011243 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:15380176..15380482 26863196 MeRIP-seq:(Medium) rs752492853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263846,Human_RBP_ID_4506654,Human_RBP_ID_5116764,Human_RBP_ID_18994499,Human_RBP_ID_26335921,Human_RBP_ID_27815243 Human_Splice_Rec_1970842,Human_Splice_Rec_1970870,Human_Splice_Rec_1970894,Human_Splice_Rec_1970922,Human_Splice_Rec_1970946 RMVar_hsa_circ_265663 55078 RMVar_ID_55078 Human_SNP_ID_659604274 m1A Human chr19 - 15396506 15396504 15396506 AGCGGTGCTGCCAAGATTGTCAGGGAGCAGGGAGCAGTAGGGAAGTGTGTTGTGCGGCATGGAGA AGCGGTGCTGCCAAGATTGTCAGGGAGCAGGG__CAGTAGGGAAGTGTGTTGTGCGGCATGGAGA GCT G AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15396504..15396787 26863196 MeRIP-seq:(Medium) rs150282702 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_52472,Human_RBP_ID_823897,Human_RBP_ID_2557936,Human_RBP_ID_6724015,Human_RBP_ID_22476532,Human_RBP_ID_23257484 GWAS_ID_6617 RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 55079 RMVar_ID_55079 Human_SNP_ID_659604407 m1A Human chr19 + 15397132 15397132 15397132 CCTCACTCAATCTACCCACAGGACAGAGGGAGAGCACTGTGGCCACTCACCCTGCGGTTCCGGTT CCTCACTCAATCTACCCACAGGACAGAGGGAGGGCACTGTGGCCACTCACCCTGCGGTTCCGGTT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15397126..15397215 26863196 MeRIP-seq:(Medium) rs760143714 Functional Loss SNV dbSNP153 33..33 33 - - - 55080 RMVar_ID_55080 Human_SNP_ID_659604752 m1A Human chr19 - 15398250 15398248 15398250 GCCTCGGGACTGCGTACTCCACTCTGCACCTCAGGGCCACCTGGCTCACGCCAGGGCATCCTTCC GCCTCGGGACTGCGTACTCCACTCTGCACCTC__GGCCACCTGGCTCACGCCAGGGCATCCTTCC CCT C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15398241..15398324 26863196 MeRIP-seq:(Medium) rs1297490551 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9328737,Human_RBP_ID_17916172,Human_RBP_ID_22069918,Human_RBP_ID_26984258 RMVar_hsa_circ_118166,RMVar_hsa_circ_67382,RMVar_hsa_circ_361138,RMVar_hsa_circ_193137,RMVar_hsa_circ_355689,RMVar_hsa_circ_316832,RMVar_hsa_circ_193138,RMVar_hsa_circ_193139 55081 RMVar_ID_55081 Human_SNP_ID_659604931 m1A Human chr19 - 15398983 15398983 15398983 CCCCAAGGTGCACTGGGGGCCTGATGCCCCTGAGGGAGGGGGCCAGCTCATCAGAGACTCAAGGT CCCCAAGGTGCACTGGGGGCCTGATGCCCCTGTGGGAGGGGGCCAGCTCATCAGAGACTCAAGGT T A AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15398933..15399134 26863196 MeRIP-seq:(Medium) rs927874065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421561,Human_RBP_ID_22069928 RMVar_hsa_circ_118166,RMVar_hsa_circ_67382,RMVar_hsa_circ_361138,RMVar_hsa_circ_193137,RMVar_hsa_circ_355689,RMVar_hsa_circ_316832,RMVar_hsa_circ_193138,RMVar_hsa_circ_193139 55082 RMVar_ID_55082 Human_SNP_ID_659605343 m1A Human chr19 - 15400342 15400342 15400342 AATTTGAAATTGTTAGGACGGAGAGGATGAGGAGGGAAAAGAGGATGGGAGAGAAGAAGGCAAAG AATTTGAAATTGTTAGGACGGAGAGGATGAGGGGGGAAAAGAGGATGGGAGAGAAGAAGGCAAAG T C AKAP8L Ensembl:ENSG00000011243 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15400173..15400443 26863196 MeRIP-seq:(Medium) rs768904362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954628,Human_RBP_ID_6724022,Human_RBP_ID_13382689,Human_RBP_ID_22501810,Human_RBP_ID_22977690,Human_RBP_ID_24545584,Human_RBP_ID_24552822,Human_RBP_ID_26335932,Human_RBP_ID_27816247 Human_Splice_Rec_1970830,Human_Splice_Rec_1970831,Human_Splice_Rec_1970856,Human_Splice_Rec_1970857,Human_Splice_Rec_1970882,Human_Splice_Rec_1970883,Human_Splice_Rec_1970908,Human_Splice_Rec_1970909,Human_Splice_Rec_1970934,Human_Splice_Rec_1970935,Human_Splice_Rec_1970962,Human_Splice_Rec_1970963,Human_Splice_Rec_1970971,Human_Splice_Rec_1970984 RMVar_hsa_circ_118166,RMVar_hsa_circ_67382,RMVar_hsa_circ_361138,RMVar_hsa_circ_193137,RMVar_hsa_circ_316832,RMVar_hsa_circ_193139 55083 RMVar_ID_55083 Human_SNP_ID_659605468 m1A Human chr19 + 15400765 15400765 15400765 CCACTCTTTAGGCCAGCTCGCCCTGCCTGCAGACAGAAAATGCCCAGCCAGAGCCACTTACCACT CCACTCTTTAGGCCAGCTCGCCCTGCCTGCAGGCAGAAAATGCCCAGCCAGAGCCACTTACCACT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15400763..15400994 26863196 MeRIP-seq:(Medium) rs767200012 Functional Loss SNV dbSNP153 33..33 33 - - - 55084 RMVar_ID_55084 Human_SNP_ID_659605471 m1A Human chr19 + 15400778 15400778 15400778 CAGCTCGCCCTGCCTGCAGACAGAAAATGCCCAGCCAGAGCCACTTACCACTCTGGAGCCCTTCT CAGCTCGCCCTGCCTGCAGACAGAAAATGCCCGGCCAGAGCCACTTACCACTCTGGAGCCCTTCT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:15400776..15401050;chr19:15400776..15401178 26863196 MeRIP-seq:(Medium) rs1181183846 Functional Loss SNV dbSNP153 33..33 33 - - - 55085 RMVar_ID_55085 Human_SNP_ID_659611716 m1A Human chr19 + 15424021 15424021 15424021 GAGTTGGGATTTGAACCCAGGTCTCGCAGGCTACAAAGCTCAGGGTGTCAGCCTTTAGCCTGAGC GAGTTGGGATTTGAACCCAGGTCTCGCAGGCTTCAAAGCTCAGGGTGTCAGCCTTTAGCCTGAGC A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15424019..15424122 26863196 MeRIP-seq:(Medium) rs1439559259 Functional Loss SNV dbSNP153 33..33 33 - - - 55086 RMVar_ID_55086 Human_SNP_ID_659612076 m1A Human chr19 - 15424921 15424921 15424921 GCGGCAGTTCGGCGTGACCGAGTGGTGCGTCAATGGCTCGCCCATCGAGACACTGAGCGAGTGGA GCGGCAGTTCGGCGTGACCGAGTGGTGCGTCAGTGGCTCGCCCATCGAGACACTGAGCGAGTGGA T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15424870..15425377 32194978 MeRIP-seq:(Medium) rs753900395 Functional Loss SNV dbSNP153 33..33 33 - - - 55087 RMVar_ID_55087 Human_SNP_ID_659612077 m1A Human chr19 - 15424921 15424921 15424921 GCGGCAGTTCGGCGTGACCGAGTGGTGCGTCAATGGCTCGCCCATCGAGACACTGAGCGAGTGGA GCGGCAGTTCGGCGTGACCGAGTGGTGCGTCACTGGCTCGCCCATCGAGACACTGAGCGAGTGGA T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15424870..15425377 32194978 MeRIP-seq:(Medium) rs753900395 Functional Loss SNV dbSNP153 33..33 33 - - - 55088 RMVar_ID_55088 Human_SNP_ID_659612967 m1A Human chr19 - 15427177 15427176 15427178 CACCACCGGGCAGCCCCCTGGGCCACTCACCAACTGCCTCTCCTCCTCCTACGGCCCGAAAGATG CACCACCGGGCAGCCCCCTGGGCCACTCACC__CTGCCTCTCCTCCTCCTACGGCCCGAAAGATG GTT G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15427126..15427280 26863196 MeRIP-seq:(Medium) rs747042474 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3954633,Human_RBP_ID_9382193,Human_RBP_ID_17916200,Human_RBP_ID_18192076,Human_RBP_ID_22069939,Human_RBP_ID_27269134,Human_RBP_ID_27473287 RMVar_hsa_circ_5794,RMVar_hsa_circ_69518 55089 RMVar_ID_55089 Human_SNP_ID_659612968 m1A Human chr19 - 15427177 15427177 15427177 CACCACCGGGCAGCCCCCTGGGCCACTCACCAACTGCCTCTCCTCCTCCTACGGCCCGAAAGATG CACCACCGGGCAGCCCCCTGGGCCACTCACCAGCTGCCTCTCCTCCTCCTACGGCCCGAAAGATG T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15427126..15427280 26863196 MeRIP-seq:(Medium) rs1168786626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954633,Human_RBP_ID_9382193,Human_RBP_ID_17916200,Human_RBP_ID_18192076,Human_RBP_ID_22069939,Human_RBP_ID_27269134,Human_RBP_ID_27473287 RMVar_hsa_circ_5794,RMVar_hsa_circ_69518 55090 RMVar_ID_55090 Human_SNP_ID_659613002 m1A Human chr19 - 15427283 15427283 15427283 CCAAAAGCCCTGGCCAAGATGATGGGCGGCGCAGGTCCTGGCAGCTCACTGGAAGCCCGCAGCCC CCAAAAGCCCTGGCCAAGATGATGGGCGGCGCTGGTCCTGGCAGCTCACTGGAAGCCCGCAGCCC T A WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15427236..15432457 32194978 MeRIP-seq:(Medium) rs565970975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514801,Human_RBP_ID_6724180,Human_RBP_ID_8478743,Human_RBP_ID_17694741,Human_RBP_ID_17916201 RMVar_hsa_circ_5794,RMVar_hsa_circ_69518 55091 RMVar_ID_55091 Human_SNP_ID_659613003 m1A Human chr19 - 15427283 15427283 15427283 CCAAAAGCCCTGGCCAAGATGATGGGCGGCGCAGGTCCTGGCAGCTCACTGGAAGCCCGCAGCCC CCAAAAGCCCTGGCCAAGATGATGGGCGGCGCGGGTCCTGGCAGCTCACTGGAAGCCCGCAGCCC T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15427236..15432457 32194978 MeRIP-seq:(Medium) rs565970975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514801,Human_RBP_ID_6724180,Human_RBP_ID_8478743,Human_RBP_ID_17694741,Human_RBP_ID_17916201 RMVar_hsa_circ_5794,RMVar_hsa_circ_69518 55092 RMVar_ID_55092 Human_SNP_ID_659614187 m1A Human chr19 - 15431150 15431150 15431150 GCCTGGGTTCTGAGGAAAACGCAATGGTGGCCATGGACTTGGGCTCTCCCTCGCTCCCTAAGAAG GCCTGGGTTCTGAGGAAAACGCAATGGTGGCCCTGGACTTGGGCTCTCCCTCGCTCCCTAAGAAG T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15431101..15431222 26863196 MeRIP-seq:(Medium) rs1418953199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514808,Human_RBP_ID_1013432,Human_RBP_ID_1555887,Human_RBP_ID_5468332,Human_RBP_ID_6724185,Human_RBP_ID_8830118,Human_RBP_ID_13383293,Human_RBP_ID_19089536 Human_Splice_Rec_1971048,Human_Splice_Rec_1971064,Human_Splice_Rec_1971100,Human_Splice_Rec_1971142,Human_Splice_Rec_1971184 RMVar_hsa_circ_69518 55093 RMVar_ID_55093 Human_SNP_ID_659614189 m1A Human chr19 + 15431155 15431155 15431155 TAGGGAGCGAGGGAGAGCCCAAGTCCATGGCCACCATTGCGTTTTCCTCAGAACCCAGGCCTGTG TAGGGAGCGAGGGAGAGCCCAAGTCCATGGCCGCCATTGCGTTTTCCTCAGAACCCAGGCCTGTG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15431105..15431211 26863196 MeRIP-seq:(Medium) rs923279032 Functional Loss SNV dbSNP153 33..33 33 - - - 55094 RMVar_ID_55094 Human_SNP_ID_659614609 m1A Human chr19 - 15432504 15432504 15432504 CCGCCGCCGCCGCCACCACCACCGCCACCGCCACCGCCGCCGCGGGACGGGCCCAAGGCCGAGCC CCGCCGCCGCCGCCACCACCACCGCCACCGCCGCCGCCGCCGCGGGACGGGCCCAAGGCCGAGCC T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:15432373..15432507;chr19:15432360..15432550 26863196 MeRIP-seq:(Medium) rs1464356003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241048,Human_RBP_ID_4506865,Human_RBP_ID_22533351 Human_Splice_Rec_1971047,Human_Splice_Rec_1971063 55095 RMVar_ID_55095 Human_SNP_ID_659614610 m1A Human chr19 - 15432504 15432504 15432504 CCGCCGCCGCCGCCACCACCACCGCCACCGCCACCGCCGCCGCGGGACGGGCCCAAGGCCGAGCC CCGCCGCCGCCGCCACCACCACCGCCACCGCCCCCGCCGCCGCGGGACGGGCCCAAGGCCGAGCC T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:15432373..15432507;chr19:15432360..15432550 26863196 MeRIP-seq:(Medium) rs1464356003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241048,Human_RBP_ID_4506865,Human_RBP_ID_22533351 Human_Splice_Rec_1971047,Human_Splice_Rec_1971063 55096 RMVar_ID_55096 Human_SNP_ID_659614622 m1A Human chr19 - 15432516 15432516 15432516 CCGCCCCCACCCCCGCCGCCGCCGCCACCACCACCGCCACCGCCACCGCCGCCGCGGGACGGGCC CCGCCCCCACCCCCGCCGCCGCCGCCACCACCGCCGCCACCGCCACCGCCGCCGCGGGACGGGCC T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15432403..15432726 26863196 MeRIP-seq:(Medium) rs1326370544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241048,Human_RBP_ID_22533351 Human_Splice_Rec_1971047,Human_Splice_Rec_1971063 55097 RMVar_ID_55097 Human_SNP_ID_659614623 m1A Human chr19 - 15432516 15432516 15432516 CCGCCCCCACCCCCGCCGCCGCCGCCACCACCACCGCCACCGCCACCGCCGCCGCGGGACGGGCC CCGCCCCCACCCCCGCCGCCGCCGCCACCACCCCCGCCACCGCCACCGCCGCCGCGGGACGGGCC T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15432403..15432726 26863196 MeRIP-seq:(Medium) rs1326370544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241048,Human_RBP_ID_22533351 Human_Splice_Rec_1971047,Human_Splice_Rec_1971063 55098 RMVar_ID_55098 Human_SNP_ID_659614646 m1A Human chr19 - 15432540 15432540 15432540 GCGGCACCCCCCGCGCCGCCGCCGCCGCCCCCACCCCCGCCGCCGCCGCCACCACCACCGCCACC GCGGCACCCCCCGCGCCGCCGCCGCCGCCCCCGCCCCCGCCGCCGCCGCCACCACCACCGCCACC T C WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr19:15432391..15432557;chr19:15432426..15432559;chr19:15432433..15432623 26863196 MeRIP-seq:(Medium) rs976574894 Functional Loss SNV dbSNP153 33..33 33 - - - 55099 RMVar_ID_55099 Human_SNP_ID_659614647 m1A Human chr19 - 15432540 15432540 15432540 GCGGCACCCCCCGCGCCGCCGCCGCCGCCCCCACCCCCGCCGCCGCCGCCACCACCACCGCCACC GCGGCACCCCCCGCGCCGCCGCCGCCGCCCCCCCCCCCGCCGCCGCCGCCACCACCACCGCCACC T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr19:15432391..15432557;chr19:15432426..15432559;chr19:15432433..15432623 26863196 MeRIP-seq:(Medium) rs976574894 Functional Loss SNV dbSNP153 33..33 33 - - - 55100 RMVar_ID_55100 Human_SNP_ID_659614661 m1A Human chr19 - 15432567 15432567 15432567 CCGCCCAGCCCCCCGAGCCCGGGCCCCGCGGCACCCCCCGCGCCGCCGCCGCCGCCCCCACCCCC CCGCCCAGCCCCCCGAGCCCGGGCCCCGCGGCCCCCCCCGCGCCGCCGCCGCCGCCCCCACCCCC T G WIZ Ensembl:ENSG00000011451 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:15432479..15432648 26863410 MeRIP-seq:(Medium) rs921929782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557297 55101 RMVar_ID_55101 Human_SNP_ID_659614704 m1A Human chr19 + 15432683 15432683 15432683 CGCCGCCTTGCTCTCCGCTTTTGTCACTCGGCACTGGGCGGTGGAGGCGGCCATCTTGGCTCCGG CGCCGCCTTGCTCTCCGCTTTTGTCACTCGGCCCTGGGCGGTGGAGGCGGCCATCTTGGCTCCGG A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15432636..15432721 26863196 MeRIP-seq:(Medium) rs1218520698 Functional Loss SNV dbSNP153 33..33 33 - - - 55102 RMVar_ID_55102 Human_SNP_ID_659619228 m1A Human chr19 - 15449851 15449851 15449851 GCGGCAGCGGCGGTAGCGGCAGCGACGGCCGCACCAAGGAGGGGAGCTCCGAGCCCCGGCACCTG GCGGCAGCGGCGGTAGCGGCAGCGACGGCCGCCCCAAGGAGGGGAGCTCCGAGCCCCGGCACCTG T G WIZ Ensembl:ENSG00000011451 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15449847..15449935 26863196 MeRIP-seq:(Medium) rs1339088334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1971077,Human_Splice_Rec_1971091,Human_Splice_Rec_1971157,Human_Splice_Rec_1971177 55103 RMVar_ID_55103 Human_SNP_ID_659619303 m1A Human chr19 + 15450060 15450044 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGG________________CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GCGCCCCCCCCACCCCA G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1182236471 Functional Loss DEL dbSNP153 18..33 33 - - - 55104 RMVar_ID_55104 Human_SNP_ID_659619307 m1A Human chr19 + 15450060 15450046 15450061 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCG_______________CCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GCCCCCCCCACCCCAC G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1313801870 Functional Loss DEL dbSNP153 20..34 33 - - - 55105 RMVar_ID_55105 Human_SNP_ID_659619308 m1A Human chr19 + 15450060 15450046 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCG______________CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GCCCCCCCCACCCCA G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1323768752 Functional Loss DEL dbSNP153 20..33 33 - - - 55106 RMVar_ID_55106 Human_SNP_ID_659619324 m1A Human chr19 + 15450060 15450054 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCC______CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG CACCCCA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1230108224 Functional Loss DEL dbSNP153 28..33 33 - - - 55107 RMVar_ID_55107 Human_SNP_ID_659619330 m1A Human chr19 + 15450060 15450056 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCCAC____CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG CCCCA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1228957915 Functional Loss DEL dbSNP153 30..33 33 - - - 55108 RMVar_ID_55108 Human_SNP_ID_659619331 m1A Human chr19 + 15450060 15450057 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCCACC___CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG CCCA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1253948291 Functional Loss DEL dbSNP153 31..33 33 - - - 55109 RMVar_ID_55109 Human_SNP_ID_659619334 m1A Human chr19 + 15450060 15450058 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCCACCC__CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG CCA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1343819701 Functional Loss DEL dbSNP153 32..33 33 - - - 55110 RMVar_ID_55110 Human_SNP_ID_659619335 m1A Human chr19 + 15450060 15450059 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCCACCCC_CCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG CA C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs1260449634 Functional Loss DEL dbSNP153 33..33 33 - - - 55111 RMVar_ID_55111 Human_SNP_ID_659619337 m1A Human chr19 + 15450060 15450060 15450060 GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCACCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG GATGGGGAGGTCCGGGGCGCCCCCCCCACCCCCCCCCCCCCCCCCTCGCCGCCCCGGGGGGGGCG A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15450026..15450179 26863196 MeRIP-seq:(Medium) rs868051053 Functional Loss SNV dbSNP153 33..33 33 - - - 55112 RMVar_ID_55112 Human_SNP_ID_659794829 m1A Human chr19 + 16067548 16067548 16067548 TCTCCTCCACCCTGCCAGGCTCACTCTGCCCCACAGCCACAGCCCCTGACTGCCGCAGCCCCCAC TCTCCTCCACCCTGCCAGGCTCACTCTGCCCCCCAGCCACAGCCCCTGACTGCCGCAGCCCCCAC A C TPM4 Ensembl:ENSG00000167460 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16067497..16067725 26863196 MeRIP-seq:(Medium) rs1393743072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1972668 55113 RMVar_ID_55113 Human_SNP_ID_659794830 m1A Human chr19 + 16067548 16067548 16067548 TCTCCTCCACCCTGCCAGGCTCACTCTGCCCCACAGCCACAGCCCCTGACTGCCGCAGCCCCCAC TCTCCTCCACCCTGCCAGGCTCACTCTGCCCCTCAGCCACAGCCCCTGACTGCCGCAGCCCCCAC A T TPM4 Ensembl:ENSG00000167460 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16067497..16067725 26863196 MeRIP-seq:(Medium) rs1393743072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1972668 55114 RMVar_ID_55114 Human_SNP_ID_659794848 m1A Human chr19 + 16067595 16067595 16067595 GACTGCCGCAGCCCCCACAGAGCCCGCCGCGCACCCCACGTCCCCCACGCCAGCGCCCAGCCATG GACTGCCGCAGCCCCCACAGAGCCCGCCGCGCCCCCCACGTCCCCCACGCCAGCGCCCAGCCATG A C TPM4 Ensembl:ENSG00000167460 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:16067448..16067725;chr19:16067398..16067793;chr19:16067415..16067799 26863196 MeRIP-seq:(Medium) rs1280251140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1972668 55115 RMVar_ID_55115 Human_SNP_ID_659795387 m1A Human chr19 - 16068996 16068996 16068996 AGCCTGTCCCGCTACCCTCACAGACCCCCACCATCTACACACAGGCTCACAAACACACCCACACT AGCCTGTCCCGCTACCCTCACAGACCCCCACCTTCTACACACAGGCTCACAAACACACCCACACT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16068880..16069227 26863196 MeRIP-seq:(Medium) rs150699706 Functional Loss SNV dbSNP153 33..33 33 - - - 55116 RMVar_ID_55116 Human_SNP_ID_659795388 m1A Human chr19 - 16068996 16068996 16068996 AGCCTGTCCCGCTACCCTCACAGACCCCCACCATCTACACACAGGCTCACAAACACACCCACACT AGCCTGTCCCGCTACCCTCACAGACCCCCACCGTCTACACACAGGCTCACAAACACACCCACACT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16068880..16069227 26863196 MeRIP-seq:(Medium) rs150699706 Functional Loss SNV dbSNP153 33..33 33 - - - 55117 RMVar_ID_55117 Human_SNP_ID_659795471 m1A Human chr19 - 16069310 16069310 16069310 ACAACCATACACACACCCCATCAGAAACACACACTCATCCATACACATTCACACACACCAACAGA ACAACCATACACACACCCCATCAGAAACACACTCTCATCCATACACATTCACACACACCAACAGA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:16069260..16069564 26863196 MeRIP-seq:(Medium) rs1422671475 Functional Loss SNV dbSNP153 33..33 33 - - - 55118 RMVar_ID_55118 Human_SNP_ID_659795472 m1A Human chr19 - 16069310 16069310 16069310 ACAACCATACACACACCCCATCAGAAACACACACTCATCCATACACATTCACACACACCAACAGA ACAACCATACACACACCCCATCAGAAACACACGCTCATCCATACACATTCACACACACCAACAGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:16069260..16069564 26863196 MeRIP-seq:(Medium) rs1422671475 Functional Loss SNV dbSNP153 33..33 33 - - - 55119 RMVar_ID_55119 Human_SNP_ID_659795501 m1A Human chr19 + 16069374 16069374 16069374 TGTGTTTCTATTGGTGTGTATGTGTGTGGATGAGTGTGTGTTTCTATTGGTGTGTGTGTATGAGT TGTGTTTCTATTGGTGTGTATGTGTGTGGATGGGTGTGTGTTTCTATTGGTGTGTGTGTATGAGT A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16069326..16070013 26863196 MeRIP-seq:(Medium) rs1179865152 Functional Loss SNV dbSNP153 33..33 33 - - - 55120 RMVar_ID_55120 Human_SNP_ID_659795502 m1A Human chr19 + 16069374 16069374 16069374 TGTGTTTCTATTGGTGTGTATGTGTGTGGATGAGTGTGTGTTTCTATTGGTGTGTGTGTATGAGT TGTGTTTCTATTGGTGTGTATGTGTGTGGATGTGTGTGTGTTTCTATTGGTGTGTGTGTATGAGT A T TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16069326..16070013 26863196 MeRIP-seq:(Medium) rs1179865152 Functional Loss SNV dbSNP153 33..33 33 - - - 55121 RMVar_ID_55121 Human_SNP_ID_659795514 m1A Human chr19 - 16069394 16069390 16069394 ACACACCAACAGAAACACACACTCATACACACACACCAATAGAAACACACACTCATCCACACACA ACACACCAACAGAAACACACACTCATACACAC____CAATAGAAACACACACTCATCCACACACA GGTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16069351..16069526 26863196 MeRIP-seq:(Medium) rs148564234 Functional Loss DEL dbSNP153 33..36 33 - - - 55122 RMVar_ID_55122 Human_SNP_ID_659795515 m1A Human chr19 - 16069394 16069390 16069394 ACACACCAACAGAAACACACACTCATACACACACACCAATAGAAACACACACTCATCCACACACA ACACACCAACAGAAACACACACTCATACACAC__ACCAATAGAAACACACACTCATCCACACACA GGTGT GGT - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16069351..16069526 26863196 MeRIP-seq:(Medium) rs148564234 Functional Loss DEL dbSNP153 33..34 33 - - - 55123 RMVar_ID_55123 Human_SNP_ID_659795520 m1A Human chr19 - 16069394 16069394 16069394 ACACACCAACAGAAACACACACTCATACACACACACCAATAGAAACACACACTCATCCACACACA ACACACCAACAGAAACACACACTCATACACACTCACCAATAGAAACACACACTCATCCACACACA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16069351..16069526 26863196 MeRIP-seq:(Medium) rs1379571668 Functional Loss SNV dbSNP153 33..33 33 - - - 55124 RMVar_ID_55124 Human_SNP_ID_659795585 m1A Human chr19 - 16069454 16069454 16069454 ACACACACTCATCCATACACATTCACACACCAATAGAAACACACACTCATTCACACACATACACA ACACACACTCATCCATACACATTCACACACCAGTAGAAACACACACTCATTCACACACATACACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16069332..16069602 26863196 MeRIP-seq:(Medium) rs903922582 Functional Loss SNV dbSNP153 33..33 33 - - - 55125 RMVar_ID_55125 Human_SNP_ID_659795686 m1A Human chr19 + 16069582 16069582 16069582 GAGTGTGTGTTTCTATTGGTGTGTGTGTTTCTATTGGTGTGTGTGGATGAATGTGTGTTTCTGTT GAGTGTGTGTTTCTATTGGTGTGTGTGTTTCTGTTGGTGTGTGTGGATGAATGTGTGTTTCTGTT A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16069576..16069660 26863196 MeRIP-seq:(Medium) rs1465867329 Functional Loss SNV dbSNP153 33..33 33 - - - 55126 RMVar_ID_55126 Human_SNP_ID_659795711 m1A Human chr19 - 16069613 16069613 16069613 AGAAACACACACTCACCCACACACACACAGCAACAGAAACACACATTCATCCACACACACCAATA AGAAACACACACTCACCCACACACACACAGCAGCAGAAACACACATTCATCCACACACACCAATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16069610..16069786 26863196 MeRIP-seq:(Medium) rs957157231 Functional Loss SNV dbSNP153 33..33 33 - - - 55127 RMVar_ID_55127 Human_SNP_ID_659795712 m1A Human chr19 - 16069613 16069613 16069613 AGAAACACACACTCACCCACACACACACAGCAACAGAAACACACATTCATCCACACACACCAATA AGAAACACACACTCACCCACACACACACAGCACCAGAAACACACATTCATCCACACACACCAATA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16069610..16069786 26863196 MeRIP-seq:(Medium) rs957157231 Functional Loss SNV dbSNP153 33..33 33 - - - 55128 RMVar_ID_55128 Human_SNP_ID_659795769 m1A Human chr19 - 16069685 16069683 16069685 CCCCATAAAAACACACACTTATCCACACACACACCCCAACAGAAACACACACTCATCCACACACA CCCCATAAAAACACACACTTATCCACACACAC__CCCAACAGAAACACACACTCATCCACACACA GGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16069660..16069794 26863196 MeRIP-seq:(Medium) rs756538233 Functional Loss DEL dbSNP153 33..34 33 - - - 55129 RMVar_ID_55129 Human_SNP_ID_659795772 m1A Human chr19 - 16069685 16069685 16069685 CCCCATAAAAACACACACTTATCCACACACACACCCCAACAGAAACACACACTCATCCACACACA CCCCATAAAAACACACACTTATCCACACACACCCCCCAACAGAAACACACACTCATCCACACACA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16069660..16069794 26863196 MeRIP-seq:(Medium) rs1176213248 Functional Loss SNV dbSNP153 33..33 33 - - - 55130 RMVar_ID_55130 Human_SNP_ID_659798430 m1A Human chr19 + 16078212 16078212 16078212 ATGGGAGCATGACAGGGGAGGCTCCAAAATGGAGGTTGAGCTGGGTCTTATAGAATAAATAAGTT ATGGGAGCATGACAGGGGAGGCTCCAAAATGGGGGTTGAGCTGGGTCTTATAGAATAAATAAGTT A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16078208..16078367 26863196 MeRIP-seq:(Medium) rs1438175319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3580966 RMVar_hsa_circ_77943,RMVar_hsa_circ_127555,RMVar_hsa_circ_111766,RMVar_hsa_circ_120213,RMVar_hsa_circ_193153,RMVar_hsa_circ_193154,RMVar_hsa_circ_193152,RMVar_hsa_circ_193155 55131 RMVar_ID_55131 Human_SNP_ID_659799523 m1A Human chr19 + 16082026 16082026 16082026 ACGGCCCTGCAGAAGCTGGAGGAGGCAGAAAAAGCTGCAGATGAGAGTGAGAGGTAAGGACGCTT ACGGCCCTGCAGAAGCTGGAGGAGGCAGAAAAGGCTGCAGATGAGAGTGAGAGGTAAGGACGCTT A G TPM4 Ensembl:ENSG00000167460 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:16081976..16082050 32194978 MeRIP-seq:(Medium) rs1358138106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825432,Human_RBP_ID_9380738,Human_RBP_ID_19089558,Human_RBP_ID_26335940 Human_Splice_Rec_1972675,Human_Splice_Rec_1972691,Human_Splice_Rec_1972707,Human_Splice_Rec_1972725,Human_Splice_Rec_1972741,Human_Splice_Rec_1972755,Human_Splice_Rec_1972769,Human_Splice_Rec_1972797,Human_Splice_Rec_1972825,Human_Splice_Rec_1972843,Human_Splice_Rec_1972855,Human_Splice_Rec_1972869,Human_Splice_Rec_1972881,Human_Splice_Rec_1972899,Human_Splice_Rec_1972915,Human_Splice_Rec_1972929,Human_Splice_Rec_1972947,Human_Splice_Rec_1972965,Human_Splice_Rec_1972977,Human_Splice_Rec_1972991,Human_Splice_Rec_1973005,Human_Splice_Rec_1973017,Human_Splice_Rec_1973031,Human_Splice_Rec_1973043,Human_Splice_Rec_1973049 Human_miRNA_ID_2013963,Human_miRNA_ID_2013964,Human_miRNA_ID_2760362,Human_miRNA_ID_2760363 RMVar_hsa_circ_8938,RMVar_hsa_circ_77943,RMVar_hsa_circ_127555,RMVar_hsa_circ_111766,RMVar_hsa_circ_120213,RMVar_hsa_circ_193153,RMVar_hsa_circ_193154,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193155,RMVar_hsa_circ_193159,RMVar_hsa_circ_274384,RMVar_hsa_circ_311721,RMVar_hsa_circ_193156,RMVar_hsa_circ_324005,RMVar_hsa_circ_282739,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193157,RMVar_hsa_circ_193158 55132 RMVar_ID_55132 Human_SNP_ID_659801248 m1A Human chr19 + 16088085 16088085 16088085 GGGTGAGCTGGAGAGGGCAGAGGAGCGTGCGGAGGTGTCTGAACTGTGAGTGGCAGAACAGGACT GGGTGAGCTGGAGAGGGCAGAGGAGCGTGCGGGGGTGTCTGAACTGTGAGTGGCAGAACAGGACT A G TPM4 Ensembl:ENSG00000167460 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr19:16088026..16088100;chr19:16087935..16088260 26863196 MeRIP-seq:(Medium) rs747231292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240491,Human_RBP_ID_515060,Human_RBP_ID_771889,Human_RBP_ID_825435,Human_RBP_ID_907476,Human_RBP_ID_5371472,Human_RBP_ID_6724669,Human_RBP_ID_9084843,Human_RBP_ID_9380742,Human_RBP_ID_17656861,Human_RBP_ID_17934900,Human_RBP_ID_19089560,Human_RBP_ID_23784788,Human_RBP_ID_24545720,Human_RBP_ID_26335943,Human_RBP_ID_27815251 Human_Splice_Rec_1972678,Human_Splice_Rec_1972679,Human_Splice_Rec_1972694,Human_Splice_Rec_1972695,Human_Splice_Rec_1972710,Human_Splice_Rec_1972711,Human_Splice_Rec_1972728,Human_Splice_Rec_1972729,Human_Splice_Rec_1972744,Human_Splice_Rec_1972745,Human_Splice_Rec_1972758,Human_Splice_Rec_1972759,Human_Splice_Rec_1972772,Human_Splice_Rec_1972773,Human_Splice_Rec_1972786,Human_Splice_Rec_1972787,Human_Splice_Rec_1972800,Human_Splice_Rec_1972801,Human_Splice_Rec_1972814,Human_Splice_Rec_1972815,Human_Splice_Rec_1972828,Human_Splice_Rec_1972829,Human_Splice_Rec_1972846,Human_Splice_Rec_1972858,Human_Splice_Rec_1972859,Human_Splice_Rec_1972872,Human_Splice_Rec_1972884,Human_Splice_Rec_1972885,Human_Splice_Rec_1972902,Human_Splice_Rec_1972903,Human_Splice_Rec_1972918,Human_Splice_Rec_1972919,Human_Splice_Rec_1972932,Human_Splice_Rec_1972933,Human_Splice_Rec_1972950,Human_Splice_Rec_1972951,Human_Splice_Rec_1972968,Human_Splice_Rec_1972969,Human_Splice_Rec_1972980,Human_Splice_Rec_1972981,Human_Splice_Rec_1972994,Human_Splice_Rec_1972995,Human_Splice_Rec_1973008,Human_Splice_Rec_1973009,Human_Splice_Rec_1973020,Human_Splice_Rec_1973021,Human_Splice_Rec_1973034,Human_Splice_Rec_1973035,Human_Splice_Rec_1973046,Human_Splice_Rec_1973047,Human_Splice_Rec_1973052,Human_Splice_Rec_1973053,Human_Splice_Rec_1973062,Human_Splice_Rec_1973063,Human_Splice_Rec_1973071 Human_miRNA_ID_2017142,Human_miRNA_ID_2017143 RMVar_hsa_circ_77943,RMVar_hsa_circ_127555,RMVar_hsa_circ_193153,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193159,RMVar_hsa_circ_311721,RMVar_hsa_circ_193156,RMVar_hsa_circ_324005,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_328874,RMVar_hsa_circ_193165,RMVar_hsa_circ_324265,RMVar_hsa_circ_193162,RMVar_hsa_circ_280606,RMVar_hsa_circ_193164 55133 RMVar_ID_55133 Human_SNP_ID_659801478 m1A Human chr19 + 16088990 16088990 16088990 CCTTTGGAAAATTTATTGTTGGGGCGATTGCTATTATTGCCGGCTGTAAGGGAAGATAAGACACA CCTTTGGAAAATTTATTGTTGGGGCGATTGCTGTTATTGCCGGCTGTAAGGGAAGATAAGACACA A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16088987..16089075 26863196 MeRIP-seq:(Medium) rs1351689137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9346698,Human_RBP_ID_22662310,Human_RBP_ID_26783709 RMVar_hsa_circ_77943,RMVar_hsa_circ_127555,RMVar_hsa_circ_193153,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_311721,RMVar_hsa_circ_193156,RMVar_hsa_circ_324005,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_328874,RMVar_hsa_circ_193165,RMVar_hsa_circ_324265,RMVar_hsa_circ_193162,RMVar_hsa_circ_280606,RMVar_hsa_circ_193164 55134 RMVar_ID_55134 Human_SNP_ID_659804970 m1A Human chr19 + 16102275 16102275 16102275 GCAGGAGGATCGCTTGAACCCAGGAAGTGGAGACTGCAGTGAGCCGATATCGCACCACAGCGCTC GCAGGAGGATCGCTTGAACCCAGGAAGTGGAGGCTGCAGTGAGCCGATATCGCACCACAGCGCTC A G TPM4 Ensembl:ENSG00000167460 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16102226..16102275 32194978 MeRIP-seq:(Medium) rs1188721503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240496,Human_RBP_ID_515087,Human_RBP_ID_6724709,Human_RBP_ID_20349041,Human_RBP_ID_26465424 Human_miRNA_ID_1541400 RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_113398,RMVar_hsa_circ_193167,RMVar_hsa_circ_266290 55135 RMVar_ID_55135 Human_SNP_ID_659805078 m1A Human chr19 + 16102791 16102791 16102791 CGTGTGGGGGCTGACTAAAGTTTACAATTCCAACTAAAAATCACCCTGCTTCTGGCTTATCTGAA CGTGTGGGGGCTGACTAAAGTTTACAATTCCACCTAAAAATCACCCTGCTTCTGGCTTATCTGAA A C TPM4 Ensembl:ENSG00000167460 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16102742..16102877 26863196 MeRIP-seq:(Medium) rs1483865979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515095,Human_RBP_ID_2558104,Human_RBP_ID_6724716,Human_RBP_ID_8198672,Human_RBP_ID_9084850,Human_RBP_ID_17009711,Human_RBP_ID_17266979,Human_RBP_ID_17382320,Human_RBP_ID_17498106,Human_RBP_ID_17694769,Human_RBP_ID_17916440,Human_RBP_ID_18301859,Human_RBP_ID_24483773,Human_RBP_ID_27464639,Human_RBP_ID_27562097,Human_RBP_ID_27675049 RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_113398,RMVar_hsa_circ_193167,RMVar_hsa_circ_266290 55136 RMVar_ID_55136 Human_SNP_ID_659807529 m1A Human chr19 - 16111950 16111950 16111950 GCGGAACAGGACACAGGTCTTCCCCACCCCCGAGTCCCCGATCAGCAGCAGCTTGAACAGGTAAT GCGGAACAGGACACAGGTCTTCCCCACCCCCGTGTCCCCGATCAGCAGCAGCTTGAACAGGTAAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:16111905..16112070;chr19:16111901..16112087;chr19:16111901..16112077 26863196 MeRIP-seq:(Medium) rs1181766596 Functional Loss SNV dbSNP153 33..33 33 - - - 55137 RMVar_ID_55137 Human_SNP_ID_659810840 m1A Human chr19 - 16124988 16124988 16124988 AGGCACAACTGAGCCCAGGAAGTCCTGACCCGACATCCACACAACTTCCAGTGACCCCACCACAG AGGCACAACTGAGCCCAGGAAGTCCTGACCCGGCATCCACACAACTTCCAGTGACCCCACCACAG T C AC008894.2 Ensembl:ENSG00000269243 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16124986..16125123 26863196 MeRIP-seq:(Medium) rs531193272 Functional Loss SNV dbSNP153 33..33 33 - - - 55138 RMVar_ID_55138 Human_SNP_ID_659811516 m1A Human chr19 + 16127497 16127497 16127497 TACTCGGGAACAAGTGTGATGTGAATGACAAGAGACAAGTTTCCAAGGAACGGGGAGAAAAGGTG TACTCGGGAACAAGTGTGATGTGAATGACAAGCGACAAGTTTCCAAGGAACGGGGAGAAAAGGTG A C RAB8A Ensembl:ENSG00000167461 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16127392..16127578 26863196 MeRIP-seq:(Medium) rs1257265855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1556017,Human_RBP_ID_1880856,Human_RBP_ID_6724747,Human_RBP_ID_8478900,Human_RBP_ID_9380746,Human_RBP_ID_18994533 Human_Splice_Rec_1973120,Human_Splice_Rec_1973121,Human_Splice_Rec_1973140,Human_Splice_Rec_1973148,Human_Splice_Rec_1973149 RMVar_hsa_circ_72330,RMVar_hsa_circ_122746,RMVar_hsa_circ_193168,RMVar_hsa_circ_103403,RMVar_hsa_circ_193169,RMVar_hsa_circ_125847,RMVar_hsa_circ_193170,RMVar_hsa_circ_108728,RMVar_hsa_circ_193172 55139 RMVar_ID_55139 Human_SNP_ID_659812665 m1A Human chr19 - 16131723 16131723 16131723 ATCCATCCCTTCCAACCAAGAACCATCCACTCATCCATCCCTTTCCAACCATCCATCTTCTTCCA ATCCATCCCTTCCAACCAAGAACCATCCACTCGTCCATCCCTTTCCAACCATCCATCTTCTTCCA T C AC008894.2 Ensembl:ENSG00000269243 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16131719..16131821 26863196 MeRIP-seq:(Medium) rs1047026268 Functional Loss SNV dbSNP153 33..33 33 - - - 55140 RMVar_ID_55140 Human_SNP_ID_659812808 m1A Human chr19 + 16132205 16132205 16132205 TTCTCAGTGATAACCTCAGAAAACCTCTTGTGATTTCAGGAAGGCAACAGCCCCCAGGGGAGCAA TTCTCAGTGATAACCTCAGAAAACCTCTTGTGCTTTCAGGAAGGCAACAGCCCCCAGGGGAGCAA A C RAB8A Ensembl:ENSG00000167461 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16132201..16132388 26863196 MeRIP-seq:(Medium) rs1305756249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914411,Human_RBP_ID_3588019,Human_RBP_ID_19089564 RMVar_hsa_circ_103403,RMVar_hsa_circ_193169 55141 RMVar_ID_55141 Human_SNP_ID_659813016 m1A Human chr19 + 16132973 16132973 16132973 GAAGCCTGGAGCAGCCTCTCCTGTCCACAGCCAGGGGTTAGGTCTGCAGGCCCGTCTGCGGTCCC GAAGCCTGGAGCAGCCTCTCCTGTCCACAGCCCGGGGTTAGGTCTGCAGGCCCGTCTGCGGTCCC A C RAB8A Ensembl:ENSG00000167461 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16132926..16133175 26863196 MeRIP-seq:(Medium) rs1486567427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769674,Human_RBP_ID_1013505,Human_RBP_ID_4507716,Human_RBP_ID_6724782,Human_RBP_ID_9380749,Human_RBP_ID_18723893 Human_miRNA_ID_336540,Human_miRNA_ID_794334,Human_miRNA_ID_960275,Human_miRNA_ID_2333290,Human_miRNA_ID_2437247,Human_miRNA_ID_2966374 RMVar_hsa_circ_103403,RMVar_hsa_circ_193169 55142 RMVar_ID_55142 Human_SNP_ID_659813021 m1A Human chr19 - 16132985 16132985 16132985 TGATGCTCGATGGGGACCGCAGACGGGCCTGCAGACCTAACCCCTGGCTGTGGACAGGAGAGGCT TGATGCTCGATGGGGACCGCAGACGGGCCTGCGGACCTAACCCCTGGCTGTGGACAGGAGAGGCT T C AC008894.2 Ensembl:ENSG00000269243 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16132936..16133036 32194978 MeRIP-seq:(Medium) rs17722795 Functional Loss SNV dbSNP153 33..33 33 - - - 55143 RMVar_ID_55143 Human_SNP_ID_659813066 m1A Human chr19 - 16133141 16133141 16133141 TCTCAGCTAGAAAGAACGTCCGATTTGGAGATAGCGGGAGGACACGAAGGAGTGGGGGCCATTTT TCTCAGCTAGAAAGAACGTCCGATTTGGAGATGGCGGGAGGACACGAAGGAGTGGGGGCCATTTT T C AC008894.2 Ensembl:ENSG00000269243 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:16133001..16133193 26863196 MeRIP-seq:(Medium) rs1568323389 Functional Loss SNV dbSNP153 33..33 33 - - - 55144 RMVar_ID_55144 Human_SNP_ID_659827342 m1A Human chr19 + 16185472 16185472 16185472 GTCATGGAGGCCTACGAGCAGGTCCAAAAGGGACCCCTGAAGCTGAAAGGCGTCGCAGAGCTGGG GTCATGGAGGCCTACGAGCAGGTCCAAAAGGGGCCCCTGAAGCTGAAAGGCGTCGCAGAGCTGGG A G FAM32A Ensembl:ENSG00000105058 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:16185401..16186461;chr19:16185401..16185843 26863196 MeRIP-seq:(Medium) rs1009736934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558184,Human_RBP_ID_5649932,Human_RBP_ID_8478923 Human_Splice_Rec_1973281,Human_Splice_Rec_1973287,Human_Splice_Rec_1973291,Human_Splice_Rec_1973299 55145 RMVar_ID_55145 Human_SNP_ID_659827372 m1A Human chr19 - 16185518 16185518 16185518 TGAAGACGGAATCCCGCGGGCCCTCGGGCCTCACCGCTTGGTCACTCCCAGCTCTGCGACGCCTT TGAAGACGGAATCCCGCGGGCCCTCGGGCCTCTCCGCTTGGTCACTCCCAGCTCTGCGACGCCTT T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:16185426..16185725;chr19:16185426..16185602 26863410 MeRIP-seq:(Medium) rs112383058 Functional Loss SNV dbSNP153 33..33 33 - - - 55146 RMVar_ID_55146 Human_SNP_ID_659827456 m1A Human chr19 + 16185683 16185683 16185683 AGCGAAACTCCTGGAAGCAATGGGAACGAGCAAAAAGAACGAGGAGGAGAAGCGGCGCGGCCTGG AGCGAAACTCCTGGAAGCAATGGGAACGAGCAGAAAGAACGAGGAGGAGAAGCGGCGCGGCCTGG A G FAM32A Ensembl:ENSG00000105058 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16185501..16185756 26863196 MeRIP-seq:(Medium) rs1189555610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55086,Human_RBP_ID_773573,Human_RBP_ID_909447,Human_RBP_ID_20433288,Human_RBP_ID_24545722,Human_RBP_ID_26337635 Human_Splice_Rec_1973277,Human_Splice_Rec_1973282,Human_Splice_Rec_1973283,Human_Splice_Rec_1973288,Human_Splice_Rec_1973289,Human_Splice_Rec_1973292,Human_Splice_Rec_1973293,Human_Splice_Rec_1973300,Human_Splice_Rec_1973301 Human_miRNA_ID_183358 55147 RMVar_ID_55147 Human_SNP_ID_659828158 m1A Human chr19 + 16188247 16188247 16188247 CAGGTTTGGAATAGGTTTTCAAGGATGAATTCAGGGTTAGCTGTTGGGTTGGATGTAAGCTGGGA CAGGTTTGGAATAGGTTTTCAAGGATGAATTCGGGGTTAGCTGTTGGGTTGGATGTAAGCTGGGA A G FAM32A Ensembl:ENSG00000105058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16188244..16188345 26863196 MeRIP-seq:(Medium) rs957649964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6724827 55148 RMVar_ID_55148 Human_SNP_ID_659828824 m1A Human chr19 + 16190910 16190910 16190910 CCTCCCCAGGACTTCAACAGACACCTGGACACACTCACGGAGCATTACGACATTCCCAAAGTCAG CCTCCCCAGGACTTCAACAGACACCTGGACACGCTCACGGAGCATTACGACATTCCCAAAGTCAG A G FAM32A Ensembl:ENSG00000105058 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16190878..16190957 26863196 MeRIP-seq:(Medium) rs761385716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55087,Human_RBP_ID_8478927 Human_Splice_Rec_1973280,Human_Splice_Rec_1973286,Human_Splice_Rec_1973290,Human_Splice_Rec_1973298 55149 RMVar_ID_55149 Human_SNP_ID_659829059 m1A Human chr19 + 16191871 16191871 16191871 GAGGGTCCAGGTGTCCGTGTTGGAGGGCTGGGATCTTGTAGGGCCTGTGCGTCCTGGCTGAGGAT GAGGGTCCAGGTGTCCGTGTTGGAGGGCTGGGGTCTTGTAGGGCCTGTGCGTCCTGGCTGAGGAT A G FAM32A Ensembl:ENSG00000105058 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16191820..16191965 26863196 MeRIP-seq:(Medium) rs917401393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515153,Human_RBP_ID_1013512,Human_RBP_ID_1556053,Human_RBP_ID_1880881,Human_RBP_ID_6724842,Human_RBP_ID_8197614,Human_RBP_ID_9380753,Human_RBP_ID_23784901,Human_RBP_ID_26335948,Human_RBP_ID_26465528,Human_RBP_ID_26984572 55150 RMVar_ID_55150 Human_SNP_ID_659830664 m1A Human chr19 + 16197989 16197989 16197989 GCCCAGCAGTCCCCACCGTCGCTGCCGCCGCCACCGCCCTCGGCCGCTGCCGAGGCCTCCTGCAG GCCCAGCAGTCCCCACCGTCGCTGCCGCCGCCGCCGCCCTCGGCCGCTGCCGAGGCCTCCTGCAG A G AP1M1 Ensembl:ENSG00000072958 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16197924..16198107 26863196 MeRIP-seq:(Medium) rs765423378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557303 Human_Splice_Rec_1973305,Human_Splice_Rec_1973329,Human_Splice_Rec_1973353,Human_Splice_Rec_1973373,Human_Splice_Rec_1973379,Human_Splice_Rec_1973403 55151 RMVar_ID_55151 Human_SNP_ID_659830684 m1A Human chr19 - 16198030 16198008 16198030 CTTCAGGTCCAGCACGTAGACGGCGCTGGCGGACATGATGGCTGCAGGAGGCCTCGGCAGCGGCC CTTCAGGTCCAGCACGTAGACGGCGCTGGCGG______________________CGGCAGCGGCC GAGGCCTCCTGCAGCCATCATGT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16197926..16198192 32194978 MeRIP-seq:(Medium) rs763234401 Functional Loss DEL dbSNP153 33..54 33 - - - 55152 RMVar_ID_55152 Human_SNP_ID_659830700 m1A Human chr19 + 16198020 16198020 16198020 CACCGCCCTCGGCCGCTGCCGAGGCCTCCTGCAGCCATCATGTCCGCCAGCGCCGTCTACGTGCT CACCGCCCTCGGCCGCTGCCGAGGCCTCCTGCCGCCATCATGTCCGCCAGCGCCGTCTACGTGCT A C AP1M1 Ensembl:ENSG00000072958 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:16197925..16198100 26863410 MeRIP-seq:(Medium) rs772766260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557303,Human_RBP_ID_8478936,Human_RBP_ID_18723906 Human_Splice_Rec_1973305,Human_Splice_Rec_1973328,Human_Splice_Rec_1973329,Human_Splice_Rec_1973353,Human_Splice_Rec_1973373,Human_Splice_Rec_1973379,Human_Splice_Rec_1973403 55153 RMVar_ID_55153 Human_SNP_ID_659830701 m1A Human chr19 + 16198020 16198020 16198020 CACCGCCCTCGGCCGCTGCCGAGGCCTCCTGCAGCCATCATGTCCGCCAGCGCCGTCTACGTGCT CACCGCCCTCGGCCGCTGCCGAGGCCTCCTGCTGCCATCATGTCCGCCAGCGCCGTCTACGTGCT A T AP1M1 Ensembl:ENSG00000072958 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:16197925..16198100 26863410 MeRIP-seq:(Medium) rs772766260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557303,Human_RBP_ID_8478936,Human_RBP_ID_18723906 Human_Splice_Rec_1973305,Human_Splice_Rec_1973328,Human_Splice_Rec_1973329,Human_Splice_Rec_1973353,Human_Splice_Rec_1973373,Human_Splice_Rec_1973379,Human_Splice_Rec_1973403 55154 RMVar_ID_55154 Human_SNP_ID_659831656 m1A Human chr19 - 16201759 16201759 16201759 CACATCTGTTCCCACCTCGGGCCTTTGCCCTGACCTGGCTCTTCTCATTTCTCAAGCCTCAGCTC CACATCTGTTCCCACCTCGGGCCTTTGCCCTGCCCTGGCTCTTCTCATTTCTCAAGCCTCAGCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16201753..16202002 26863196 MeRIP-seq:(Medium) rs1246022061 Functional Loss SNV dbSNP153 33..33 33 - - - 55155 RMVar_ID_55155 Human_SNP_ID_659838624 m1A Human chr19 + 16228914 16228914 16228914 GGGTCCCCGAGAACAGCGAGATCGTGTGGTCCATCAAGTCCTTCCCGGTGAGCACTCTGTCCAGA GGGTCCCCGAGAACAGCGAGATCGTGTGGTCCGTCAAGTCCTTCCCGGTGAGCACTCTGTCCAGA A G AP1M1 Ensembl:ENSG00000072958 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16228901..16228950 26863196 MeRIP-seq:(Medium) rs773324732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380757,Human_RBP_ID_18996999,Human_RBP_ID_19092606 Human_Splice_Rec_1973321,Human_Splice_Rec_1973347,Human_Splice_Rec_1973397,Human_Splice_Rec_1973443 RMVar_hsa_circ_14053,RMVar_hsa_circ_82897,RMVar_hsa_circ_87228,RMVar_hsa_circ_84337,RMVar_hsa_circ_193176,RMVar_hsa_circ_193177,RMVar_hsa_circ_108029,RMVar_hsa_circ_193180,RMVar_hsa_circ_111151,RMVar_hsa_circ_193181,RMVar_hsa_circ_24931,RMVar_hsa_circ_193183,RMVar_hsa_circ_109860,RMVar_hsa_circ_193184 55156 RMVar_ID_55156 Human_SNP_ID_659865544 m1A Human chr19 - 16324916 16324916 16324916 GCAGGATGGGTTCACTCAGCGCCATGGCCGGGACCCGGGGAGAAAGGACGCGGACGGGGACACCG GCAGGATGGGTTCACTCAGCGCCATGGCCGGGGCCCGGGGAGAAAGGACGCGGACGGGGACACCG T C lnc-EPS15L1-2 RNACentral:URS00008C2AE8 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16324865..16325423 26863196 MeRIP-seq:(Medium) rs1469179909 Functional Loss SNV dbSNP153 33..33 33 - - - 55157 RMVar_ID_55157 Human_SNP_ID_659865559 m1A Human chr19 - 16324946 16324946 16324946 GGCACGGGCTGGCGAAAGTGGAGAAGGACGGCAGGATGGGTTCACTCAGCGCCATGGCCGGGACC GGCACGGGCTGGCGAAAGTGGAGAAGGACGGCTGGATGGGTTCACTCAGCGCCATGGCCGGGACC T A lnc-EPS15L1-2 RNACentral:URS00008C2AE8 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16324826..16325526 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 55158 RMVar_ID_55158 Human_SNP_ID_659876387 m1A Human chr19 + 16364452 16364452 16364452 TATCCCCAGATGTCCCTCCCACCTTCAGCTCTACTGCGGCCTCCTCCTACCCCGACCTCCCCGGG TATCCCCAGATGTCCCTCCCACCTTCAGCTCTGCTGCGGCCTCCTCCTACCCCGACCTCCCCGGG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16364447..16364552 26863196 MeRIP-seq:(Medium) rs1343636582 Functional Loss SNV dbSNP153 33..33 33 - - - 55159 RMVar_ID_55159 Human_SNP_ID_659877449 m1A Human chr19 - 16368501 16368426 16368501 TGTGTGGGATCACCTGTTGTGTAGGGTGAATGACAGTTGTGTGGGTGTCTGTGTTCTGCAGGATG TGTGTGGGATCACCTGTTGTGTAGGGTGAATG_________________________________ CCATTCATCCTACACAACAGAGGATGCCCACACAATTGTCATTCATCCTGCAGAACACAGACACCCACACAACTGT C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16368451..16368757 26863196 MeRIP-seq:(Medium) rs1568391600 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_515203,Human_RBP_ID_2558279,Human_RBP_ID_23785116 RMVar_hsa_circ_51449,RMVar_hsa_circ_328011 55160 RMVar_ID_55160 Human_SNP_ID_659877456 m1A Human chr19 - 16368461 16368461 16368461 GTGGGTGTCTGTGTTCTGCAGGATGAATGACAATTGTGTGGGCATCCTCTGTTGTGTAGGATGAA GTGGGTGTCTGTGTTCTGCAGGATGAATGACAGTTGTGTGGGCATCCTCTGTTGTGTAGGATGAA T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16368455..16368820 26863196 MeRIP-seq:(Medium) rs1362746027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093725,Human_RBP_ID_2558278,Human_RBP_ID_5292725,Human_RBP_ID_23785116 RMVar_hsa_circ_51449,RMVar_hsa_circ_328011 55161 RMVar_ID_55161 Human_SNP_ID_659877469 m1A Human chr19 - 16368501 16368501 16368501 TGTGTGGGATCACCTGTTGTGTAGGGTGAATGACAGTTGTGTGGGTGTCTGTGTTCTGCAGGATG TGTGTGGGATCACCTGTTGTGTAGGGTGAATGGCAGTTGTGTGGGTGTCTGTGTTCTGCAGGATG T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16368451..16368757 26863196 MeRIP-seq:(Medium) rs976402530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515203,Human_RBP_ID_2558279,Human_RBP_ID_23785116 RMVar_hsa_circ_51449,RMVar_hsa_circ_328011 55162 RMVar_ID_55162 Human_SNP_ID_659877491 m1A Human chr19 + 16368562 16368562 16368562 CACATCTCTCGTTCATCCTGCACAACATGCACACCCACACAACTGTTATTCATTCCACACAACAG CACATCTCTCGTTCATCCTGCACAACATGCACGCCCACACAACTGTTATTCATTCCACACAACAG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16368512..16368762 26863196 MeRIP-seq:(Medium) rs1447133964 Functional Loss SNV dbSNP153 33..33 33 - - - 55163 RMVar_ID_55163 Human_SNP_ID_659900979 m1A Human chr19 + 16458650 16458650 16458650 CCAGTCCTGAAAGTGCTCCCTGGCCATCTCCTACCTTGCCGGGCTGATTTCACTCCACACACACA CCAGTCCTGAAAGTGCTCCCTGGCCATCTCCTGCCTTGCCGGGCTGATTTCACTCCACACACACA A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16458639..16458734 26863196 MeRIP-seq:(Medium) rs73511183 Functional Loss SNV dbSNP153 33..33 33 - - - 55164 RMVar_ID_55164 Human_SNP_ID_659904559 m1A Human chr19 + 16471932 16471932 16471932 GCCCGGCCCGTACCTGCTGGGAGAGGGGGATGAGCGGCGCCGCCATCTTCCCGCGGACTCGGGCT GCCCGGCCCGTACCTGCTGGGAGAGGGGGATGCGCGGCGCCGCCATCTTCCCGCGGACTCGGGCT A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16471701..16471936 26863196 MeRIP-seq:(Medium) rs1407204052 Functional Loss SNV dbSNP153 33..33 33 - - - 55165 RMVar_ID_55165 Human_SNP_ID_659917525 m1A Human chr19 + 16518810 16518810 16518810 TCCTGCACATGCTCCTCCTGGAGCCTAGGAGGAGGCTTCAATCTGACTTAGGGCAGATGCACATC TCCTGCACATGCTCCTCCTGGAGCCTAGGAGGCGGCTTCAATCTGACTTAGGGCAGATGCACATC A C C19orf44 Ensembl:ENSG00000105072 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16495850..16553829 32194978 MeRIP-seq:(Medium) rs1219298036 Functional Loss SNV dbSNP153 33..33 33 - - - 55166 RMVar_ID_55166 Human_SNP_ID_659918017 m1A Human chr19 - 16520203 16520203 16520203 CCGCTCCCGGTCCCAGTCGCGGTCCCGGTCCAAGTCGTACTCCCCAGGAAGAAGACGCCGGTCAC CCGCTCCCGGTCCCAGTCGCGGTCCCGGTCCAGGTCGTACTCCCCAGGAAGAAGACGCCGGTCAC T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16520094..16520438 26863196 MeRIP-seq:(Medium) rs779311631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54918,Human_RBP_ID_515273,Human_RBP_ID_1013557,Human_RBP_ID_1880945,Human_RBP_ID_8830273,Human_RBP_ID_22446531,Human_RBP_ID_27464774 Human_Splice_Rec_1973980,Human_Splice_Rec_1973981,Human_Splice_Rec_1974012,Human_Splice_Rec_1974013,Human_Splice_Rec_1974030,Human_Splice_Rec_1974031,Human_Splice_Rec_1974038 55167 RMVar_ID_55167 Human_SNP_ID_659918040 m1A Human chr19 + 16520246 16520246 16520246 CCGCGACTGGGACCGGGAGCGGCTTCTGGAGGAGCGCGACCTGCTCCGACTTCTGCAGGGAAGGG CCGCGACTGGGACCGGGAGCGGCTTCTGGAGGGGCGCGACCTGCTCCGACTTCTGCAGGGAAGGG A G C19orf44 Ensembl:ENSG00000105072 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16520198..16520264 26863196 MeRIP-seq:(Medium) rs1404243205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241302 55168 RMVar_ID_55168 Human_SNP_ID_659919785 m1A Human chr19 - 16525391 16525391 16525391 ACACTTCCGGGGGCCCTTCCCGCCCCACCAGCAGCACCCGCAGTTCAACCAGCCTCCGCACCCCC ACACTTCCGGGGGCCCTTCCCGCCCCACCAGCGGCACCCGCAGTTCAACCAGCCTCCGCACCCCC T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:16525226..16525550 26863410 MeRIP-seq:(Medium) rs1250168448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387299,Human_RBP_ID_18192078,Human_RBP_ID_22065563,Human_RBP_ID_27816258 Human_miRNA_ID_272432 RMVar_hsa_circ_35824 55169 RMVar_ID_55169 Human_SNP_ID_659921054 m1A Human chr19 - 16529602 16529602 16529602 TCAGCTCAGCCTGCCCCCAGGAAACAGCCCCCAGAGGCTGGGCACCGAGTGTAGTCAGAAAGCAG TCAGCTCAGCCTGCCCCCAGGAAACAGCCCCCGGAGGCTGGGCACCGAGTGTAGTCAGAAAGCAG T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16529599..16529771 26863196 MeRIP-seq:(Medium) rs150179770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19089586 55170 RMVar_ID_55170 Human_SNP_ID_659922974 m1A Human chr19 - 16535507 16535507 16535507 CCAGGGCGCGCCATCCATGGACGAGCTCATCCAGCAGAGCCAGTGGAACCTCCAGCAGCAGGAGC CCAGGGCGCGCCATCCATGGACGAGCTCATCCGGCAGAGCCAGTGGAACCTCCAGCAGCAGGAGC T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16535410..16535647 26863196 MeRIP-seq:(Medium) rs942072981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54946,Human_RBP_ID_1880954,Human_RBP_ID_3564195,Human_RBP_ID_8479107,Human_RBP_ID_18440707 Human_Splice_Rec_1973957,Human_Splice_Rec_1973989,Human_Splice_Rec_1974041 RMVar_hsa_circ_267066,RMVar_hsa_circ_378968 55171 RMVar_ID_55171 Human_SNP_ID_659923423 m1A Human chr19 + 16537121 16537121 16537121 CTCTAAACGATTTCTCAGACAAGACTCACTCCAGATCTTCACCTCCCCTTTATCTCAGCCTGGTG CTCTAAACGATTTCTCAGACAAGACTCACTCCGGATCTTCACCTCCCCTTTATCTCAGCCTGGTG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16537119..16537390 26863196 MeRIP-seq:(Medium) rs1457199207 Functional Loss SNV dbSNP153 33..33 33 - - - 55172 RMVar_ID_55172 Human_SNP_ID_659923901 m1A Human chr19 - 16538848 16538848 16538848 ACCTGATGGTGTAATGAGCAGGGGAGGAAGACACCTCAGACGGTGCTTTGGCTTGGGTGACTGAG ACCTGATGGTGTAATGAGCAGGGGAGGAAGACGCCTCAGACGGTGCTTTGGCTTGGGTGACTGAG T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16538844..16539096 26863196 MeRIP-seq:(Medium) rs1479423230 Functional Loss SNV dbSNP153 33..33 33 - - - 55173 RMVar_ID_55173 Human_SNP_ID_659925162 m1A Human chr19 - 16542402 16542402 16542402 GACGGCGCTGGTGGTCGATCGTGTGGCGCCGGAGGACGTTCCCCGCGGCCGGAGCCATGGAGATG GACGGCGCTGGTGGTCGATCGTGTGGCGCCGGTGGACGTTCCCCGCGGCCGGAGCCATGGAGATG T A CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:16542314..16542450;chr19:16542321..16542425;chr19:16542317..16542426 26863196 MeRIP-seq:(Medium) rs373816390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54953,Human_RBP_ID_3954652,Human_RBP_ID_4508123,Human_RBP_ID_18440708,Human_RBP_ID_27816262 Human_Splice_Rec_1973953,Human_Splice_Rec_1973985,Human_Splice_Rec_1974045 55174 RMVar_ID_55174 Human_SNP_ID_659925163 m1A Human chr19 - 16542402 16542402 16542402 GACGGCGCTGGTGGTCGATCGTGTGGCGCCGGAGGACGTTCCCCGCGGCCGGAGCCATGGAGATG GACGGCGCTGGTGGTCGATCGTGTGGCGCCGGGGGACGTTCCCCGCGGCCGGAGCCATGGAGATG T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:16542314..16542450;chr19:16542321..16542425;chr19:16542317..16542426 26863196 MeRIP-seq:(Medium) rs373816390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54953,Human_RBP_ID_3954652,Human_RBP_ID_4508123,Human_RBP_ID_18440708,Human_RBP_ID_27816262 Human_Splice_Rec_1973953,Human_Splice_Rec_1973985,Human_Splice_Rec_1974045 55175 RMVar_ID_55175 Human_SNP_ID_659925303 m1A Human chr19 + 16542694 16542694 16542694 AAGGCTGGAACGGCGCGGGTGGGTGTTAGTCGAGACCGGGGGGCGCGGGGCGTGCCCCTTGGTCG AAGGCTGGAACGGCGCGGGTGGGTGTTAGTCGCGACCGGGGGGCGCGGGGCGTGCCCCTTGGTCG A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:16542643..16542783;chr19:16542658..16542766 26863196 MeRIP-seq:(Medium) rs1179448520 Functional Loss SNV dbSNP153 33..33 33 - - - 55176 RMVar_ID_55176 Human_SNP_ID_659925343 m1A Human chr19 - 16542804 16542804 16542804 AGTCTCCTCACTGTGCCCGCGAAAGGAAAGAGACCCTGGCCCAGGCACGAAGTCCCCAGGCCCCT AGTCTCCTCACTGTGCCCGCGAAAGGAAAGAGCCCCTGGCCCAGGCACGAAGTCCCCAGGCCCCT T G AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16542676..16542821 26863196 MeRIP-seq:(Medium) rs1340449401 Functional Loss SNV dbSNP153 33..33 33 - - - 55177 RMVar_ID_55177 Human_SNP_ID_659933534 m1A Human chr19 + 16572045 16572045 16572045 CGAAGGCGAGCGGTAGCACGTAGCGCGGGTAGAAGCGCGGCGGCAGCAGCGGGCCGGACGACGGA CGAAGGCGAGCGGTAGCACGTAGCGCGGGTAGGAGCGCGGCGGCAGCAGCGGGCCGGACGACGGA A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16572001..16572200 26863196 MeRIP-seq:(Medium) rs1465301555 Functional Loss SNV dbSNP153 33..33 33 - - - 55178 RMVar_ID_55178 Human_SNP_ID_659935016 m1A Human chr19 + 16576579 16576579 16576579 TCAAAGGTGAGCTTCCGCTCTTTTAACCGGACAGGCTTGACGCCCGCCTCAGCCACCTGCCCGTC TCAAAGGTGAGCTTCCGCTCTTTTAACCGGACGGGCTTGACGCCCGCCTCAGCCACCTGCCCGTC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16576528..16576599 26863196 MeRIP-seq:(Medium) rs747986847 Functional Loss SNV dbSNP153 33..33 33 - - - 55179 RMVar_ID_55179 Human_SNP_ID_659935245 m1A Human chr19 - 16577029 16577029 16577029 GACGAGACTCCGGGGCCTCCCCATCCCAAGGGACCCCCTCGCTGCTCTTTCAGTCCTCGGAACTC GACGAGACTCCGGGGCCTCCCCATCCCAAGGGGCCCCCTCGCTGCTCTTTCAGTCCTCGGAACTC T C AC008764.1,MED26 Ensembl:ENSG00000141979,Ensembl:ENSG00000105085 Protein coding,Protein coding CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16576731..16577176 32194978 MeRIP-seq:(Medium) rs143376680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27464884 Human_miRNA_ID_1485304,Human_miRNA_ID_1485305 55180 RMVar_ID_55180 Human_SNP_ID_659945704 m1A Human chr19 + 16619809 16619809 16619809 TGCACCCAGCACACGAATACCCGAGTCTCCACAGCAGCCACGAGGCTGACCCACCACCAGGGTGT TGCACCCAGCACACGAATACCCGAGTCTCCACGGCAGCCACGAGGCTGACCCACCACCAGGGTGT A G AC008764.2 Ensembl:ENSG00000268087 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16619697..16619848 26863196 MeRIP-seq:(Medium) rs1336728802 Functional Loss SNV dbSNP153 33..33 33 - - - 55181 RMVar_ID_55181 Human_SNP_ID_659945705 m1A Human chr19 + 16619809 16619809 16619809 TGCACCCAGCACACGAATACCCGAGTCTCCACAGCAGCCACGAGGCTGACCCACCACCAGGGTGT TGCACCCAGCACACGAATACCCGAGTCTCCACTGCAGCCACGAGGCTGACCCACCACCAGGGTGT A T AC008764.2 Ensembl:ENSG00000268087 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:16619697..16619848 26863196 MeRIP-seq:(Medium) rs1336728802 Functional Loss SNV dbSNP153 33..33 33 - - - 55182 RMVar_ID_55182 Human_SNP_ID_659947796 m1A Human chr19 - 16627889 16627889 16627889 CGCAGCAGATCAGGGACCGGCTGCTGCAGGCCATCGACCCCCAGAGCAACGTAAGTACCCGCCGC CGCAGCAGATCAGGGACCGGCTGCTGCAGGCCGTCGACCCCCAGAGCAACGTAAGTACCCGCCGC T C AC008764.4,AC008764.1,MED26 Ensembl:ENSG00000268790,Ensembl:ENSG00000141979,Ensembl:ENSG00000105085 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16577669..16628155 32194978 MeRIP-seq:(Medium) rs534357438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1973863,Human_Splice_Rec_1974099,Human_Splice_Rec_1974103,Human_Splice_Rec_1974119 55183 RMVar_ID_55183 Human_SNP_ID_659947810 m1A Human chr19 + 16627925 16627925 16627925 CTGCAGCAGCCGGTCCCTGATCTGCTGCGGAGACGCCGGAGCCGCTGTCATTGCCTGGGCGAGGC CTGCAGCAGCCGGTCCCTGATCTGCTGCGGAGCCGCCGGAGCCGCTGTCATTGCCTGGGCGAGGC A C AC008764.2 Ensembl:ENSG00000268087 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16627878..16628179 26863196 MeRIP-seq:(Medium) rs112290724 Functional Loss SNV dbSNP153 33..33 33 - - - 55184 RMVar_ID_55184 Human_SNP_ID_659947840 m1A Human chr19 + 16627994 16627984 16627994 GGTTGCGGCCGGGCCAGCGGGCGGGCGGGCTGAGGCGGGGGACGGGGGTCACTCACTCGCCGGCC GGTTGCGGCCGGGCCAGCGGGCG__________GGCGGGGGACGGGGGTCACTCACTCGCCGGCC GGGCGGGCTGA G AC008764.2 Ensembl:ENSG00000268087 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16627951..16628164 26863196 MeRIP-seq:(Medium) rs1360466147 Functional Loss DEL dbSNP153 24..33 33 - - - 55185 RMVar_ID_55185 Human_SNP_ID_659956492 m1A Human chr19 - 16659445 16659445 16659445 AAAGTGGACACTGTCTGCTCCTCTTTGTAGGAAAAAGAAGGACACGCAGGGCTTTGGGGAGGAGT AAAGTGGACACTGTCTGCTCCTCTTTGTAGGACAAAGAAGGACACGCAGGGCTTTGGGGAGGAGT T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16659376..16659450 26863196 MeRIP-seq:(Medium) rs962401116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907493,Human_RBP_ID_4508396,Human_RBP_ID_18997025,Human_RBP_ID_19092639,Human_RBP_ID_22545761,Human_RBP_ID_22591392 Human_Splice_Rec_1974124,Human_Splice_Rec_1974125,Human_Splice_Rec_1974134,Human_Splice_Rec_1974135,Human_Splice_Rec_1974146,Human_Splice_Rec_1974147,Human_Splice_Rec_1974160,Human_Splice_Rec_1974161,Human_Splice_Rec_1974170,Human_Splice_Rec_1974171,Human_Splice_Rec_1974178,Human_Splice_Rec_1974179,Human_Splice_Rec_1974190,Human_Splice_Rec_1974191,Human_Splice_Rec_1974204,Human_Splice_Rec_1974205,Human_Splice_Rec_1974212,Human_Splice_Rec_1974213,Human_Splice_Rec_1974220,Human_Splice_Rec_1974221,Human_Splice_Rec_1974230,Human_Splice_Rec_1974231,Human_Splice_Rec_1974240,Human_Splice_Rec_1974241,Human_Splice_Rec_1974248,Human_Splice_Rec_1974249,Human_Splice_Rec_1974258,Human_Splice_Rec_1974259,Human_Splice_Rec_1974266,Human_Splice_Rec_1974267,Human_Splice_Rec_1974276,Human_Splice_Rec_1974277,Human_Splice_Rec_1974286,Human_Splice_Rec_1974287,Human_Splice_Rec_1974296,Human_Splice_Rec_1974297,Human_Splice_Rec_1974302,Human_Splice_Rec_1974303,Human_Splice_Rec_1974310,Human_Splice_Rec_1974311,Human_Splice_Rec_1974318,Human_Splice_Rec_1974319,Human_Splice_Rec_1974324,Human_Splice_Rec_1974325,Human_Splice_Rec_1974334,Human_Splice_Rec_1974335,Human_Splice_Rec_1974344,Human_Splice_Rec_1974345,Human_Splice_Rec_1974354,Human_Splice_Rec_1974355,Human_Splice_Rec_1974368,Human_Splice_Rec_1974369 Human_miRNA_ID_2381514 RMVar_hsa_circ_193206,RMVar_hsa_circ_370533 55186 RMVar_ID_55186 Human_SNP_ID_659956758 m1A Human chr19 - 16659986 16659986 16659986 GTAATTCTCCCTCTGCAGGACGTTGCTGATGAATGCCGGGGCGGTGCTGAACTTTAAGCTGTGAG GTAATTCTCCCTCTGCAGGACGTTGCTGATGAGTGCCGGGGCGGTGCTGAACTTTAAGCTGTGAG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding CDS,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:16659424..16660115 32194978 MeRIP-seq:(Medium) rs1265692395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909453,Human_RBP_ID_4558192,Human_RBP_ID_5371479,Human_RBP_ID_8479227,Human_RBP_ID_9380764,Human_RBP_ID_13389500,Human_RBP_ID_18997026,Human_RBP_ID_19089594,Human_RBP_ID_23785589 Human_Splice_Rec_1974122,Human_Splice_Rec_1974123,Human_Splice_Rec_1974133,Human_Splice_Rec_1974144,Human_Splice_Rec_1974145,Human_Splice_Rec_1974158,Human_Splice_Rec_1974159,Human_Splice_Rec_1974168,Human_Splice_Rec_1974169,Human_Splice_Rec_1974176,Human_Splice_Rec_1974177,Human_Splice_Rec_1974188,Human_Splice_Rec_1974189,Human_Splice_Rec_1974202,Human_Splice_Rec_1974203,Human_Splice_Rec_1974210,Human_Splice_Rec_1974211,Human_Splice_Rec_1974219,Human_Splice_Rec_1974228,Human_Splice_Rec_1974229,Human_Splice_Rec_1974238,Human_Splice_Rec_1974239,Human_Splice_Rec_1974246,Human_Splice_Rec_1974247,Human_Splice_Rec_1974256,Human_Splice_Rec_1974257,Human_Splice_Rec_1974264,Human_Splice_Rec_1974265,Human_Splice_Rec_1974274,Human_Splice_Rec_1974275,Human_Splice_Rec_1974284,Human_Splice_Rec_1974285,Human_Splice_Rec_1974294,Human_Splice_Rec_1974295,Human_Splice_Rec_1974300,Human_Splice_Rec_1974301,Human_Splice_Rec_1974316,Human_Splice_Rec_1974317,Human_Splice_Rec_1974323,Human_Splice_Rec_1974332,Human_Splice_Rec_1974333,Human_Splice_Rec_1974342,Human_Splice_Rec_1974343,Human_Splice_Rec_1974352,Human_Splice_Rec_1974353,Human_Splice_Rec_1974360,Human_Splice_Rec_1974361,Human_Splice_Rec_1974366,Human_Splice_Rec_1974367 55187 RMVar_ID_55187 Human_SNP_ID_659956765 m1A Human chr19 - 16660002 16660002 16660002 GGCGCCCCTAGTAACTGTAATTCTCCCTCTGCAGGACGTTGCTGATGAATGCCGGGGCGGTGCTG GGCGCCCCTAGTAACTGTAATTCTCCCTCTGCCGGACGTTGCTGATGAATGCCGGGGCGGTGCTG T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16659951..16660025 26863196 MeRIP-seq:(Medium) rs1269928026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560122,Human_RBP_ID_5376044,Human_RBP_ID_9382241,Human_RBP_ID_18997026 Human_Splice_Rec_1974123,Human_Splice_Rec_1974133,Human_Splice_Rec_1974145,Human_Splice_Rec_1974159,Human_Splice_Rec_1974169,Human_Splice_Rec_1974177,Human_Splice_Rec_1974189,Human_Splice_Rec_1974203,Human_Splice_Rec_1974211,Human_Splice_Rec_1974219,Human_Splice_Rec_1974229,Human_Splice_Rec_1974239,Human_Splice_Rec_1974247,Human_Splice_Rec_1974257,Human_Splice_Rec_1974265,Human_Splice_Rec_1974275,Human_Splice_Rec_1974285,Human_Splice_Rec_1974295,Human_Splice_Rec_1974301,Human_Splice_Rec_1974317,Human_Splice_Rec_1974323,Human_Splice_Rec_1974333,Human_Splice_Rec_1974343,Human_Splice_Rec_1974353,Human_Splice_Rec_1974361,Human_Splice_Rec_1974367 55188 RMVar_ID_55188 Human_SNP_ID_659957279 m1A Human chr19 - 16661281 16661281 16661281 GACGATGAAGTAACTGAGGTCGAAGACGGGGAAGAGCGGCACCCGCGAGAAGCTGAGCGCCAGTT GACGATGAAGTAACTGAGGTCGAAGACGGGGAGGAGCGGCACCCGCGAGAAGCTGAGCGCCAGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:16661162..16661290 26863196 MeRIP-seq:(Medium) rs201283889 Functional Loss SNV dbSNP153 33..33 33 - - - 55189 RMVar_ID_55189 Human_SNP_ID_660003316 m1A Human chr19 + 16829451 16829451 16829451 ACATGGCGCACGCTGGCGGTGGCAGCGGTGGCAGCGGTGCCGGCGGCCCCGCGGGCCGGGGGCTG ACATGGCGCACGCTGGCGGTGGCAGCGGTGGCGGCGGTGCCGGCGGCCCCGCGGGCCGGGGGCTG A G SIN3B Ensembl:ENSG00000127511 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16829401..16829622 26863196 MeRIP-seq:(Medium) rs1056992434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773815,Human_RBP_ID_910889,Human_RBP_ID_9382242,Human_RBP_ID_18421301,Human_RBP_ID_18997029,Human_RBP_ID_22977898,Human_RBP_ID_26335962,Human_RBP_ID_27816264 Human_Splice_Rec_1974737,Human_Splice_Rec_1974773,Human_Splice_Rec_1974787 55190 RMVar_ID_55190 Human_SNP_ID_660005449 m1A Human chr19 + 16837118 16837118 16837118 GGTTGCTGTGGGCAGGACCTGTTTCATGAGGGACTGTTCCTGGTGGGGAGTGATGGCCTGAGGTG GGTTGCTGTGGGCAGGACCTGTTTCATGAGGGGCTGTTCCTGGTGGGGAGTGATGGCCTGAGGTG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16837116..16837206 26863196 MeRIP-seq:(Medium) rs1436498103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2558656,Human_RBP_ID_9427131,Human_RBP_ID_13389705 RMVar_hsa_circ_77626,RMVar_hsa_circ_346912,RMVar_hsa_circ_23373,RMVar_hsa_circ_26759,RMVar_hsa_circ_193214 55191 RMVar_ID_55191 Human_SNP_ID_660006075 m1A Human chr19 + 16839491 16839491 16839491 CCCCATTTTGTCGCAGTGGCACACTTTAGGGGATCAGAGGGTGCATGCGGAGCTTGGAAATGCCT CCCCATTTTGTCGCAGTGGCACACTTTAGGGGGTCAGAGGGTGCATGCGGAGCTTGGAAATGCCT A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16839483..16839626 32194978 MeRIP-seq:(Medium) rs1415952423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13389776 RMVar_hsa_circ_77626,RMVar_hsa_circ_346912,RMVar_hsa_circ_23373,RMVar_hsa_circ_26759,RMVar_hsa_circ_193214 55192 RMVar_ID_55192 Human_SNP_ID_660010502 m1A Human chr19 + 16855676 16855676 16855676 CCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTCCAGCCTGGGTGGCGACAAG CCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCATTGTACTCCAGCCTGGGTGGCGACAAG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1463394296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13390135,Human_RBP_ID_25442548 RMVar_hsa_circ_77626,RMVar_hsa_circ_20290,RMVar_hsa_circ_373268,RMVar_hsa_circ_193214,RMVar_hsa_circ_62081,RMVar_hsa_circ_193218,RMVar_hsa_circ_90072,RMVar_hsa_circ_41396,RMVar_hsa_circ_193219 55193 RMVar_ID_55193 Human_SNP_ID_660013250 m1A Human chr19 + 16865623 16865623 16865623 AGATCATCGAGAGCCTCAAGAAGAACCCTGTCACCGCTGTCCCCGTTGTCCTGAAAAGGTGCCCT AGATCATCGAGAGCCTCAAGAAGAACCCTGTCGCCGCTGTCCCCGTTGTCCTGAAAAGGTGCCCT A G SIN3B Ensembl:ENSG00000127511 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16865576..16869603 32194978 MeRIP-seq:(Medium) rs1213935583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380769,Human_RBP_ID_18724160,Human_RBP_ID_24545459,Human_RBP_ID_27815270 Human_Splice_Rec_1974757,Human_Splice_Rec_1974809,Human_Splice_Rec_1974843,Human_Splice_Rec_1974859 Human_miRNA_ID_2627674,Human_miRNA_ID_2748510,Human_miRNA_ID_2878152 RMVar_hsa_circ_77626,RMVar_hsa_circ_373268,RMVar_hsa_circ_193214,RMVar_hsa_circ_193218,RMVar_hsa_circ_48791,RMVar_hsa_circ_193222,RMVar_hsa_circ_269527,RMVar_hsa_circ_302830,RMVar_hsa_circ_307803,RMVar_hsa_circ_360531,RMVar_hsa_circ_193223,RMVar_hsa_circ_337369 55194 RMVar_ID_55194 Human_SNP_ID_660017370 m1A Human chr19 + 16878654 16878654 16878654 CGAGGACATGGTACCCTGCAAGACGCTGTGTGAGACAGTGCACGTGCACGGCCTGCCCGTGACCC CGAGGACATGGTACCCTGCAAGACGCTGTGTGTGACAGTGCACGTGCACGGCCTGCCCGTGACCC A T SIN3B Ensembl:ENSG00000127511 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:16878604..16878698 26863196 MeRIP-seq:(Medium) rs775898027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910902,Human_RBP_ID_5526894,Human_RBP_ID_27562121 55195 RMVar_ID_55195 Human_SNP_ID_660017566 m1A Human chr19 - 16879245 16879245 16879245 CTGAGGGCCTGAACACCAGCCAGGCAGAGCTGATGCCCAAACCCTCAGATGATGTTTCTGGCAGC CTGAGGGCCTGAACACCAGCCAGGCAGAGCTGGTGCCCAAACCCTCAGATGATGTTTCTGGCAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:16879201..16879450 26863196 MeRIP-seq:(Medium) rs949388543 Functional Loss SNV dbSNP153 33..33 33 - - - 55196 RMVar_ID_55196 Human_SNP_ID_660068194 m1A Human chr19 - 17060031 17060031 17060031 CTGCAGTCCACGTTGCTGGAAGGGCATGGCACAGCTCCACCTGACCTGGATCTCTCTGCTATTAA CTGCAGTCCACGTTGCTGGAAGGGCATGGCACGGCTCCACCTGACCTGGATCTCTCTGCTATTAA T C HAUS8 Ensembl:ENSG00000131351 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17059614..17060160 26863196 MeRIP-seq:(Medium) rs776034655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4508522,Human_RBP_ID_6725792,Human_RBP_ID_19092660,Human_RBP_ID_26337660 Human_Splice_Rec_1975244,Human_Splice_Rec_1975245,Human_Splice_Rec_1975266,Human_Splice_Rec_1975267,Human_Splice_Rec_1975284,Human_Splice_Rec_1975285,Human_Splice_Rec_1975304,Human_Splice_Rec_1975305,Human_Splice_Rec_1975322,Human_Splice_Rec_1975323,Human_Splice_Rec_1975333 RMVar_hsa_circ_193226,RMVar_hsa_circ_119212,RMVar_hsa_circ_375462,RMVar_hsa_circ_21838,RMVar_hsa_circ_290562,RMVar_hsa_circ_193227,RMVar_hsa_circ_90512,RMVar_hsa_circ_300969,RMVar_hsa_circ_193228,RMVar_hsa_circ_355822,RMVar_hsa_circ_300463,RMVar_hsa_circ_193230,RMVar_hsa_circ_23780 55197 RMVar_ID_55197 Human_SNP_ID_660070516 m1A Human chr19 + 17069085 17069085 17069085 TACTGCAGATACCGGGACTCAATCACTCTTCCACCTGTGGGGACACACTGTTGGTGCACAACAAA TACTGCAGATACCGGGACTCAATCACTCTTCCGCCTGTGGGGACACACTGTTGGTGCACAACAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17069051..17069100 26863196 MeRIP-seq:(Medium) rs749416737 Functional Loss SNV dbSNP153 33..33 33 - - - 55198 RMVar_ID_55198 Human_SNP_ID_660072352 m1A Human chr19 + 17075293 17075293 17075293 TCAGGGGCCCGCGCAGTTCCTGGCGGGGTCGAACCCGAACTCACCCCGAGGGTCCTAACTCCCCA TCAGGGGCCCGCGCAGTTCCTGGCGGGGTCGATCCCGAACTCACCCCGAGGGTCCTAACTCCCCA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17075206..17075378 26863196 MeRIP-seq:(Medium) rs570083257 Functional Loss SNV dbSNP153 33..33 33 - - - 55199 RMVar_ID_55199 Human_SNP_ID_660072648 m1A Human chr19 - 17075824 17075824 17075824 CGCCGCCGGTCCCGGGCCGGGTCCCCGGCCGGACGACCGCCTGCCAGCCCGCCGCTGCTCGAGCC CGCCGCCGGTCCCGGGCCGGGTCCCCGGCCGGCCGACCGCCTGCCAGCCCGCCGCTGCTCGAGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:17075776..17075961;chr19:17075776..17076580;chr19:17075776..17101890;chr19:17075776..17076044 26863196 MeRIP-seq:(Medium) rs1163766965 Functional Loss SNV dbSNP153 33..33 33 - - - 55200 RMVar_ID_55200 Human_SNP_ID_660079719 m1A Human chr19 + 17101704 17101704 17101704 CGCGCCCCGAGCCTGGGAGGCATGCTGAAGCCAGGCGGCCGGCAGGATGAGTGTGAAAGAGGCAG CGCGCCCCGAGCCTGGGAGGCATGCTGAAGCCGGGCGGCCGGCAGGATGAGTGTGAAAGAGGCAG A G MYO9B Ensembl:ENSG00000099331 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:17075778..17101910;chr19:17101646..17101902;chr19:17101646..17101818 26863196 MeRIP-seq:(Medium) rs1362291763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770351,Human_RBP_ID_4558195 Human_Splice_Rec_1975344,Human_Splice_Rec_1975418 RMVar_hsa_circ_39561,RMVar_hsa_circ_122375,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_193232,RMVar_hsa_circ_269844,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_193234,RMVar_hsa_circ_6029 55201 RMVar_ID_55201 Human_SNP_ID_660092019 m1A Human chr19 - 17146272 17146272 17146272 TGTGATGGATGGATTCATGAGTGTATGGGTAGATCCACTCATGAATGCATCCATCCACCCATGAA TGTGATGGATGGATTCATGAGTGTATGGGTAGGTCCACTCATGAATGCATCCATCCACCCATGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17146269..17146608 26863196 MeRIP-seq:(Medium) rs994586873 Functional Loss SNV dbSNP153 33..33 33 - - - 55202 RMVar_ID_55202 Human_SNP_ID_660105146 m1A Human chr19 + 17194622 17194622 17194622 GAAGAGAAGGAGAGGGAAGCCCTGGAAGCCGCAAGAGCAGGTGCTGAGGAGGGCGGACAGGGTCA GAAGAGAAGGAGAGGGAAGCCCTGGAAGCCGCGAGAGCAGGTGCTGAGGAGGGCGGACAGGGTCA A G MYO9B Ensembl:ENSG00000099331 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:17193042..17194888;chr19:17194551..17194924 26863196 MeRIP-seq:(Medium) rs755750782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825326,Human_RBP_ID_5526906,Human_RBP_ID_5585454,Human_RBP_ID_9382276,Human_RBP_ID_24545465,Human_RBP_ID_26337675 Human_Splice_Rec_1975384,Human_Splice_Rec_1975458,Human_Splice_Rec_1975532,Human_Splice_Rec_1975604 RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_118441,RMVar_hsa_circ_264888,RMVar_hsa_circ_193262 55203 RMVar_ID_55203 Human_SNP_ID_660105319 m1A Human chr19 + 17195066 17195066 17195066 CTTCTAGTCGTAGAGACGGAGGCTGAGAACACATCTCAAAAGCAGCCCACAGAGCAACCCCAGGC CTTCTAGTCGTAGAGACGGAGGCTGAGAACACCTCTCAAAAGCAGCCCACAGAGCAACCCCAGGC A C MYO9B Ensembl:ENSG00000099331 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17195016..17195152 26863196 MeRIP-seq:(Medium) rs1431695222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27815299 RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_118441,RMVar_hsa_circ_264888,RMVar_hsa_circ_193262 55204 RMVar_ID_55204 Human_SNP_ID_660105322 m1A Human chr19 + 17195074 17195074 17195074 CGTAGAGACGGAGGCTGAGAACACATCTCAAAAGCAGCCCACAGAGCAACCCCAGGCCATGGCAG CGTAGAGACGGAGGCTGAGAACACATCTCAAAGGCAGCCCACAGAGCAACCCCAGGCCATGGCAG A G MYO9B Ensembl:ENSG00000099331 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr19:17195024..17195238;chr19:17195026..17195075 26863196,32194978 MeRIP-seq:(Medium) rs772581423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22065629,Human_RBP_ID_27815299 RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_118441,RMVar_hsa_circ_264888,RMVar_hsa_circ_193262 55205 RMVar_ID_55205 Human_SNP_ID_660105469 m1A Human chr19 - 17195383 17195383 17195383 GGCTGAGCATGGCACTAGGGCTGGCGGCGGCCACCAGCTTCTTGCCCCGCCACAGTTCCACGGCG GGCTGAGCATGGCACTAGGGCTGGCGGCGGCCCCCAGCTTCTTGCCCCGCCACAGTTCCACGGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17195332..17195436 26863196 MeRIP-seq:(Medium) rs1267510546 Functional Loss SNV dbSNP153 33..33 33 - - - 55206 RMVar_ID_55206 Human_SNP_ID_660109895 m1A Human chr19 - 17209711 17209711 17209711 AAGAGGTCCCGCCCCCACGATCACCGGTACTCACAGCATTTTGTCGCAGGAGCGAAAGCCTGCGG AAGAGGTCCCGCCCCCACGATCACCGGTACTCGCAGCATTTTGTCGCAGGAGCGAAAGCCTGCGG T C lnc-NR2F6-5 RNACentral:URS0000D585C7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17209706..17209849 26863196 MeRIP-seq:(Medium) rs1176180100 Functional Loss SNV dbSNP153 33..33 33 - - - 55207 RMVar_ID_55207 Human_SNP_ID_660110251 m1A Human chr19 - 17210764 17210752 17210764 CCTCATCGCCGCCGGCTGCCTCCTCCTCCAGCAGCACCTCCAGCTCCTCCTCCTGGATGTCCCGG CCTCATCGCCGCCGGCTGCCTCCTCCTCCAGC____________TCCTCCTCCTGGATGTCCCGG AGCTGGAGGTGCT A lnc-NR2F6-5 RNACentral:URS0000D585C7 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17210699..17210802 26863196 MeRIP-seq:(Medium) rs1198138089 Functional Loss DEL dbSNP153 33..44 33 - - - 55208 RMVar_ID_55208 Human_SNP_ID_660111885 m1A Human chr19 - 17215446 17215446 17215446 GTTTCTCCGCTGCCATCGCCTCGCAGCGGGATAGCAGCCGCACCAGGTTTAGCTCCAGCCTCGAC GTTTCTCCGCTGCCATCGCCTCGCAGCGGGATGGCAGCCGCACCAGGTTTAGCTCCAGCCTCGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17215395..17215905 26863196 MeRIP-seq:(Medium) rs866900872 Functional Loss SNV dbSNP153 33..33 33 - - - 55209 RMVar_ID_55209 Human_SNP_ID_660112058 m1A Human chr19 - 17215761 17215761 17215761 GAAAAGTGGATTGTCACCCGGGGGTCTTTCCCATGTCCTGATCATGGGAGTCGGGGGGGCGGGGC GAAAAGTGGATTGTCACCCGGGGGTCTTTCCCGTGTCCTGATCATGGGAGTCGGGGGGGCGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17215759..17215879 26863196 MeRIP-seq:(Medium) rs769199408 Functional Loss SNV dbSNP153 33..33 33 - - - 55210 RMVar_ID_55210 Human_SNP_ID_660112202 m1A Human chr19 - 17216088 17216088 17216088 CCAAAGTGAGCGGTGATGGGGGCTGAGGGGGCAGGGGCACCCCTTCTCACCAGCTTCTCGGCTTG CCAAAGTGAGCGGTGATGGGGGCTGAGGGGGCGGGGGCACCCCTTCTCACCAGCTTCTCGGCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17216087..17216157 26863196 MeRIP-seq:(Medium) rs372540938 Functional Loss SNV dbSNP153 33..33 33 - - - 55211 RMVar_ID_55211 Human_SNP_ID_660115770 m1A Human chr19 - 17226919 17226919 17226919 GAAACCGGAGTCCCTCAAACTGGAGGGGCTAAATCTTTTGCCTAGAGGCCCGGCCTGGGGACCCC GAAACCGGAGTCCCTCAAACTGGAGGGGCTAAGTCTTTTGCCTAGAGGCCCGGCCTGGGGACCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17226908..17227000 26863196 MeRIP-seq:(Medium) rs746340167 Functional Loss SNV dbSNP153 33..33 33 - - - 55212 RMVar_ID_55212 Human_SNP_ID_660116586 m1A Human chr19 - 17229029 17229029 17229029 CAAACTGAAGAGGCATTTGCAATCCAGGAGAAAGCGACCCCTGGTAGGGGGAGCTGCAAGAGGAA CAAACTGAAGAGGCATTTGCAATCCAGGAGAAGGCGACCCCTGGTAGGGGGAGCTGCAAGAGGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17228678..17229121 32194978 MeRIP-seq:(Medium) rs754924838 Functional Loss SNV dbSNP153 33..33 33 - - - 55213 RMVar_ID_55213 Human_SNP_ID_660117562 m1A Human chr19 + 17232125 17232125 17232125 GCTGTCCTAGGATTGGACCCTCCATCCTGGACAGGGGTCCTGGGGAGGATGAGGCTGAGGCCTGG GCTGTCCTAGGATTGGACCCTCCATCCTGGACGGGGGTCCTGGGGAGGATGAGGCTGAGGCCTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:17231901..17232131 32194978 MeRIP-seq:(Medium) rs1290725914 Functional Loss SNV dbSNP153 33..33 33 - - - 55214 RMVar_ID_55214 Human_SNP_ID_660117645 m1A Human chr19 - 17232423 17232423 17232423 TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCATTGAGACACTGATCAGAGACATGCTGCTGTCG TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCGTTGAGACACTGATCAGAGACATGCTGCTGTCG T C NR2F6 Ensembl:ENSG00000160113 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17232376..17232575 26863196 MeRIP-seq:(Medium) rs765130843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54286,Human_RBP_ID_515577,Human_RBP_ID_1881066,Human_RBP_ID_4563523,Human_RBP_ID_8839204,Human_RBP_ID_9293516,Human_RBP_ID_13390884,Human_RBP_ID_17916809,Human_RBP_ID_18440730,Human_RBP_ID_22071011,Human_RBP_ID_26984938,Human_RBP_ID_27269735 Human_miRNA_ID_2769358 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_94273,RMVar_hsa_circ_193286,RMVar_hsa_circ_193284 55215 RMVar_ID_55215 Human_SNP_ID_660117646 m1A Human chr19 - 17232423 17232423 17232423 TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCATTGAGACACTGATCAGAGACATGCTGCTGTCG TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCCTTGAGACACTGATCAGAGACATGCTGCTGTCG T G NR2F6 Ensembl:ENSG00000160113 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17232376..17232575 26863196 MeRIP-seq:(Medium) rs765130843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54286,Human_RBP_ID_515577,Human_RBP_ID_1881066,Human_RBP_ID_4563523,Human_RBP_ID_8839204,Human_RBP_ID_9293516,Human_RBP_ID_13390884,Human_RBP_ID_17916809,Human_RBP_ID_18440730,Human_RBP_ID_22071011,Human_RBP_ID_26984938,Human_RBP_ID_27269735 Human_miRNA_ID_2769358 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_94273,RMVar_hsa_circ_193286,RMVar_hsa_circ_193284 55216 RMVar_ID_55216 Human_SNP_ID_660118740 m1A Human chr19 - 17235844 17235844 17235844 CAGGGGGCGGCGCGGCGGGCGCGGTGCTGGGCATCGACAACGTGTGCGAGCTGGCGGCGCGGCTG CAGGGGGCGGCGCGGCGGGCGCGGTGCTGGGCTTCGACAACGTGTGCGAGCTGGCGGCGCGGCTG T A NR2F6 Ensembl:ENSG00000160113 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17235607..17236090 26863196 MeRIP-seq:(Medium) rs1275857402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4563536,Human_RBP_ID_5468377,Human_RBP_ID_5499041,Human_RBP_ID_17916813,Human_RBP_ID_27465003 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284,RMVar_hsa_circ_193287,RMVar_hsa_circ_126511 55217 RMVar_ID_55217 Human_SNP_ID_660118741 m1A Human chr19 - 17235844 17235844 17235844 CAGGGGGCGGCGCGGCGGGCGCGGTGCTGGGCATCGACAACGTGTGCGAGCTGGCGGCGCGGCTG CAGGGGGCGGCGCGGCGGGCGCGGTGCTGGGCGTCGACAACGTGTGCGAGCTGGCGGCGCGGCTG T C NR2F6 Ensembl:ENSG00000160113 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17235607..17236090 26863196 MeRIP-seq:(Medium) rs1275857402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4563536,Human_RBP_ID_5468377,Human_RBP_ID_5499041,Human_RBP_ID_17916813,Human_RBP_ID_27465003 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284,RMVar_hsa_circ_193287,RMVar_hsa_circ_126511 55218 RMVar_ID_55218 Human_SNP_ID_660118744 m1A Human chr19 + 17235852 17235852 17235852 CCGCCAGCTCGCACACGTTGTCGATGCCCAGCACCGCGCCCGCCGCGCCGCCCCCTGCGCCGAAG CCGCCAGCTCGCACACGTTGTCGATGCCCAGCGCCGCGCCCGCCGCGCCGCCCCCTGCGCCGAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17235808..17236078 26863196 MeRIP-seq:(Medium) rs1359275827 Functional Loss SNV dbSNP153 33..33 33 - - - 55219 RMVar_ID_55219 Human_SNP_ID_660118851 m1A Human chr19 - 17236048 17236048 17236048 CCCCGCCTCCCGCAGCGGTGCAGCGCGGCCGCATCCCGCACTCGCTGCCTGGTGCCGTGGCCGCC CCCCGCCTCCCGCAGCGGTGCAGCGCGGCCGCTTCCCGCACTCGCTGCCTGGTGCCGTGGCCGCC T A AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17236001..17236075 26863196 MeRIP-seq:(Medium) rs1030004933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557315,Human_RBP_ID_5130307,Human_RBP_ID_5321512,Human_RBP_ID_5468379,Human_RBP_ID_17082372,Human_RBP_ID_17568496,Human_RBP_ID_18946658,Human_RBP_ID_22071904,Human_RBP_ID_27465008 Human_Splice_Rec_1975934,Human_Splice_Rec_1975940,Human_Splice_Rec_1975948 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284,RMVar_hsa_circ_193287,RMVar_hsa_circ_126511 55220 RMVar_ID_55220 Human_SNP_ID_660118852 m1A Human chr19 - 17236048 17236048 17236048 CCCCGCCTCCCGCAGCGGTGCAGCGCGGCCGCATCCCGCACTCGCTGCCTGGTGCCGTGGCCGCC CCCCGCCTCCCGCAGCGGTGCAGCGCGGCCGCGTCCCGCACTCGCTGCCTGGTGCCGTGGCCGCC T C AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17236001..17236075 26863196 MeRIP-seq:(Medium) rs1030004933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557315,Human_RBP_ID_5130307,Human_RBP_ID_5321512,Human_RBP_ID_5468379,Human_RBP_ID_17082372,Human_RBP_ID_17568496,Human_RBP_ID_18946658,Human_RBP_ID_22071904,Human_RBP_ID_27465008 Human_Splice_Rec_1975934,Human_Splice_Rec_1975940,Human_Splice_Rec_1975948 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284,RMVar_hsa_circ_193287,RMVar_hsa_circ_126511 55221 RMVar_ID_55221 Human_SNP_ID_660120281 m1A Human chr19 + 17240764 17240764 17240764 GTGGTGCTGGTCGATCTGGCAGTCACGGTTGGACCTGGGGGCACACAGAAGCCAGGGCTCCCTGA GTGGTGCTGGTCGATCTGGCAGTCACGGTTGGCCCTGGGGGCACACAGAAGCCAGGGCTCCCTGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr19:17240726..17240775;chr19:17232451..17244264 26863196,32194978 MeRIP-seq:(Medium) rs1317314233 Functional Loss SNV dbSNP153 33..33 33 - - - 55222 RMVar_ID_55222 Human_SNP_ID_660121801 m1A Human chr19 - 17245739 17245739 17245739 AGGCCCGGAGCGGCAGCCGCGGGCGCCGGGGGACCCAGGGGGCGCGGCGATCAGCCCCGGCGCGC AGGCCCGGAGCGGCAGCCGCGGGCGCCGGGGGGCCCAGGGGGCGCGGCGATCAGCCCCGGCGCGC T C AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:17245651..17245900;chr19:17245394..17245890 26863410 MeRIP-seq:(Medium) rs1046492307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559352,Human_RBP_ID_9329886 55223 RMVar_ID_55223 Human_SNP_ID_660121812 m1A Human chr19 - 17245763 17245763 17245763 GAGGCGCCGGCCCAGCGGCCCTGCAGGCCCGGAGCGGCAGCCGCGGGCGCCGGGGGACCCAGGGG GAGGCGCCGGCCCAGCGGCCCTGCAGGCCCGGGGCGGCAGCCGCGGGCGCCGGGGGACCCAGGGG T C AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:17245078..17245925;chr19:17245714..17245846 26863196 MeRIP-seq:(Medium) rs1315381306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773114,Human_RBP_ID_4508808,Human_RBP_ID_9329886 55224 RMVar_ID_55224 Human_SNP_ID_660121826 m1A Human chr19 + 17245799 17245799 17245799 GGCCTGCAGGGCCGCTGGGCCGGCGCCTCTGGAGCTGCCGCCCCCGCTGCGGCCGCTCCTGCCTG GGCCTGCAGGGCCGCTGGGCCGGCGCCTCTGGCGCTGCCGCCCCCGCTGCGGCCGCTCCTGCCTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17245701..17245850 26863196 MeRIP-seq:(Medium) rs1027984530 Functional Loss SNV dbSNP153 33..33 33 - - - 55225 RMVar_ID_55225 Human_SNP_ID_660121850 m1A Human chr19 - 17245863 17245863 17245863 CGCGCGGGGTCGGTGGCGGTGGCGGCGGCGAGAGCGAGGCTTGGGCCCAGGCGCAGGCCCAGGCC CGCGCGGGGTCGGTGGCGGTGGCGGCGGCGAGGGCGAGGCTTGGGCCCAGGCGCAGGCCCAGGCC T C AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17245626..17245925 26863196 MeRIP-seq:(Medium) rs1219296229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557324,Human_RBP_ID_9328770 55226 RMVar_ID_55226 Human_SNP_ID_660128590 m1A Human chr19 + 17267509 17267509 17267509 AGTGAGTCGGCGGCTGATTTAGAAGGAGGTTCAGGCTACGGTGAGCCGAAGGTGGGTGGTGAAAG AGTGAGTCGGCGGCTGATTTAGAAGGAGGTTCGGGCTACGGTGAGCCGAAGGTGGGTGGTGAAAG A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17267451..17269024 26863196 MeRIP-seq:(Medium) rs748998301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907519,Human_RBP_ID_5116775,Human_RBP_ID_5499046,Human_RBP_ID_9382279,Human_RBP_ID_19092683 Human_Splice_Rec_1976073,Human_Splice_Rec_1976083,Human_Splice_Rec_1976099,Human_Splice_Rec_1976115,Human_Splice_Rec_1976127,Human_Splice_Rec_1976135,Human_Splice_Rec_1976141,Human_Splice_Rec_1976157,Human_Splice_Rec_1976173,Human_Splice_Rec_1976183,Human_Splice_Rec_1976195,Human_Splice_Rec_1976205,Human_Splice_Rec_1976213,Human_Splice_Rec_1976257 55227 RMVar_ID_55227 Human_SNP_ID_660130633 m1A Human chr19 - 17274026 17274026 17274026 ACCCCAGGGCACCCAGCGCCTGCCGCAGCCTCACCCAGGCCGTGTCATCGTTCACCACCACCAGT ACCCCAGGGCACCCAGCGCCTGCCGCAGCCTCTCCCAGGCCGTGTCATCGTTCACCACCACCAGT T A USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17273976..17276537 26863196 MeRIP-seq:(Medium) rs1250494857 Functional Loss SNV dbSNP153 33..33 33 - - - 55228 RMVar_ID_55228 Human_SNP_ID_660131344 m1A Human chr19 + 17276497 17276497 17276497 TCTGACTGCTCCCTCCTCCCGGGTATGCAGCCAGCAGAAAACTGAGCTTCCGGTCACAGAGAACG TCTGACTGCTCCCTCCTCCCGGGTATGCAGCCCGCAGAAAACTGAGCTTCCGGTCACAGAGAACG A C AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17276476..17276500 26863196 MeRIP-seq:(Medium) rs1044961359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907521,Human_RBP_ID_22665096 Human_Splice_Rec_1976078,Human_Splice_Rec_1976092,Human_Splice_Rec_1976110,Human_Splice_Rec_1976126,Human_Splice_Rec_1976140,Human_Splice_Rec_1976152,Human_Splice_Rec_1976168,Human_Splice_Rec_1976194,Human_Splice_Rec_1976212,Human_Splice_Rec_1976218,Human_Splice_Rec_1976234,Human_Splice_Rec_1976244,Human_Splice_Rec_1976266 RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_322263,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_111991,RMVar_hsa_circ_115721,RMVar_hsa_circ_295755,RMVar_hsa_circ_193297,RMVar_hsa_circ_270986,RMVar_hsa_circ_193298,RMVar_hsa_circ_193299 55229 RMVar_ID_55229 Human_SNP_ID_660131364 m1A Human chr19 + 17276535 17276535 17276535 AAACTGAGCTTCCGGTCACAGAGAACGTGCAGACGATTCCCCCGCCATATGTGGTCCGCACCATC AAACTGAGCTTCCGGTCACAGAGAACGTGCAGTCGATTCCCCCGCCATATGTGGTCCGCACCATC A T AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17276476..17276575 26863196 MeRIP-seq:(Medium) rs1478335310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515595,Human_RBP_ID_1881070,Human_RBP_ID_8479386 Human_Splice_Rec_1976078,Human_Splice_Rec_1976079,Human_Splice_Rec_1976092,Human_Splice_Rec_1976093,Human_Splice_Rec_1976110,Human_Splice_Rec_1976111,Human_Splice_Rec_1976126,Human_Splice_Rec_1976140,Human_Splice_Rec_1976152,Human_Splice_Rec_1976153,Human_Splice_Rec_1976168,Human_Splice_Rec_1976169,Human_Splice_Rec_1976194,Human_Splice_Rec_1976212,Human_Splice_Rec_1976218,Human_Splice_Rec_1976219,Human_Splice_Rec_1976234,Human_Splice_Rec_1976244,Human_Splice_Rec_1976249,Human_Splice_Rec_1976266,Human_Splice_Rec_1976267 Human_miRNA_ID_2147374,Human_miRNA_ID_2946339,Human_miRNA_ID_2988800,Human_miRNA_ID_3022501 RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_322263,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_111991,RMVar_hsa_circ_115721,RMVar_hsa_circ_295755,RMVar_hsa_circ_193297,RMVar_hsa_circ_270986,RMVar_hsa_circ_193298,RMVar_hsa_circ_193299 55230 RMVar_ID_55230 Human_SNP_ID_660131367 m1A Human chr19 - 17276540 17276540 17276540 ACAAGGATGGTGCGGACCACATATGGCGGGGGAATCGTCTGCACGTTCTCTGTGACCGGAAGCTC ACAAGGATGGTGCGGACCACATATGGCGGGGGGATCGTCTGCACGTTCTCTGTGACCGGAAGCTC T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:17276476..17276625 32194978 MeRIP-seq:(Medium) rs751745605 Functional Loss SNV dbSNP153 33..33 33 - - - 55231 RMVar_ID_55231 Human_SNP_ID_660131710 m1A Human chr19 - 17277566 17277566 17277566 GATGTGAAGGCCCAGCAGGGCCTGGGGAGTCCAAGAGGGATGGATGCTCCAGGCTGAGGGTGCAG GATGTGAAGGCCCAGCAGGGCCTGGGGAGTCCGAGAGGGATGGATGCTCCAGGCTGAGGGTGCAG T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:17277563..17277645 32194978 MeRIP-seq:(Medium) rs1352802435 Functional Loss SNV dbSNP153 33..33 33 - - - 55232 RMVar_ID_55232 Human_SNP_ID_660132183 m1A Human chr19 - 17279072 17279072 17279072 AAGGCTTTAGGCCAAGGACTTCCTTGCACAAGAAGGTGCAGATGTACAGGGATGGTTCAGACAGT AAGGCTTTAGGCCAAGGACTTCCTTGCACAAGGAGGTGCAGATGTACAGGGATGGTTCAGACAGT T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17279026..17279200 26863196 MeRIP-seq:(Medium) rs757714650 Functional Loss SNV dbSNP153 33..33 33 - - - 55233 RMVar_ID_55233 Human_SNP_ID_660132196 m1A Human chr19 + 17279129 17279129 17279129 AAAGCCTTGGTTCTCAAACTGGGTTCCTTGGGACCTCCGGGGTGGGGGGGTTCCAGGAGGCACGT AAAGCCTTGGTTCTCAAACTGGGTTCCTTGGGGCCTCCGGGGTGGGGGGGTTCCAGGAGGCACGT A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17279079..17279246 26863196 MeRIP-seq:(Medium) rs1167754133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770813,Human_RBP_ID_5145701,Human_RBP_ID_17656863,Human_RBP_ID_18165685 RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 55234 RMVar_ID_55234 Human_SNP_ID_660139402 m1A Human chr19 - 17301129 17301129 17301129 GCGCCCCAAGAGGACCATCCATATTGACTGTGAGAAGCGCATCACTAGCTGCAAAGGCGCCCAGG GCGCCCCAAGAGGACCATCCATATTGACTGTGGGAAGCGCATCACTAGCTGCAAAGGCGCCCAGG T C ABHD8 Ensembl:ENSG00000127220 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17301038..17301636 26863196 MeRIP-seq:(Medium) rs764146908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8479415 RMVar_hsa_circ_193303,RMVar_hsa_circ_80680,RMVar_hsa_circ_276459,RMVar_hsa_circ_193302 55235 RMVar_ID_55235 Human_SNP_ID_660139419 m1A Human chr19 - 17301167 17301167 17301167 AGCGGCAGTGGCAGTGGTGGGCGGCGGCGGCGAGCCAGGCGCCCCAAGAGGACCATCCATATTGA AGCGGCAGTGGCAGTGGTGGGCGGCGGCGGCGTGCCAGGCGCCCCAAGAGGACCATCCATATTGA T A ABHD8 Ensembl:ENSG00000127220 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17301122..17301231 26863196 MeRIP-seq:(Medium) rs777148469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193303,RMVar_hsa_circ_80680,RMVar_hsa_circ_276459,RMVar_hsa_circ_193302 55236 RMVar_ID_55236 Human_SNP_ID_660140127 m1A Human chr19 + 17303291 17303291 17303291 GGCCCGGGTCGGGGCGGAGGGGTCCCAGGCGGAGAAGCCAGCGTCCGCCTGCTGGCGCCGTTTAC GGCCCGGGTCGGGGCGGAGGGGTCCCAGGCGGTGAAGCCAGCGTCCGCCTGCTGGCGCCGTTTAC A T MRPL34 Ensembl:ENSG00000130312 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17303226..17303400 26863196 MeRIP-seq:(Medium) rs937057412 Functional Loss SNV dbSNP153 33..33 33 - - - 55237 RMVar_ID_55237 Human_SNP_ID_660141034 m1A Human chr19 + 17306261 17306245 17306261 GGCCCGGGGCAAGGCTCGCGGGAATGAGTATCAGCCGAGCAACATCAAACGCAAGAACAAGCACG GGCCCGGGGCAAGGCTC________________GCCGAGCAACATCAAACGCAAGAACAAGCACG CGCGGGAATGAGTATCA C MRPL34 Ensembl:ENSG00000130312 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17306212..17306297 26863196 MeRIP-seq:(Medium) rs758780869 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_1013632,Human_RBP_ID_1556276,Human_RBP_ID_4560127,Human_RBP_ID_17916847,Human_RBP_ID_27269807 Human_Splice_Rec_1976424,Human_Splice_Rec_1976430,Human_Splice_Rec_1976434,Human_Splice_Rec_1976436,Human_Splice_Rec_1976438 RMVar_hsa_circ_84596,RMVar_hsa_circ_193304 55238 RMVar_ID_55238 Human_SNP_ID_660141044 m1A Human chr19 + 17306261 17306261 17306261 GGCCCGGGGCAAGGCTCGCGGGAATGAGTATCAGCCGAGCAACATCAAACGCAAGAACAAGCACG GGCCCGGGGCAAGGCTCGCGGGAATGAGTATCGGCCGAGCAACATCAAACGCAAGAACAAGCACG A G MRPL34 Ensembl:ENSG00000130312 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17306212..17306297 26863196 MeRIP-seq:(Medium) rs372170364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013632,Human_RBP_ID_1556276,Human_RBP_ID_4560127,Human_RBP_ID_17916847,Human_RBP_ID_27269807 Human_Splice_Rec_1976424,Human_Splice_Rec_1976430,Human_Splice_Rec_1976434,Human_Splice_Rec_1976436,Human_Splice_Rec_1976438 RMVar_hsa_circ_84596,RMVar_hsa_circ_193304 55239 RMVar_ID_55239 Human_SNP_ID_660141994 m1A Human chr19 - 17309610 17309583 17309610 CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCCACCGCCGCCACCAGAGCCGCCTTCTTAGCCGCC CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCC___________________________GCCGCC CTAAGAAGGCGGCTCTGGTGGCGGCGGT C ABHD8 Ensembl:ENSG00000127220 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17309549..17309830 26863196 MeRIP-seq:(Medium) rs1335759961 Functional Loss DEL dbSNP153 33..59 33 - - - 55240 RMVar_ID_55240 Human_SNP_ID_660142003 m1A Human chr19 - 17309610 17309604 17309610 CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCCACCGCCGCCACCAGAGCCGCCTTCTTAGCCGCC CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCC______GCCACCAGAGCCGCCTTCTTAGCCGCC CGGCGGT C ABHD8 Ensembl:ENSG00000127220 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17309549..17309830 26863196 MeRIP-seq:(Medium) rs757606453 Functional Loss DEL dbSNP153 33..38 33 - - - 55241 RMVar_ID_55241 Human_SNP_ID_660142008 m1A Human chr19 - 17309610 17309610 17309610 CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCCACCGCCGCCACCAGAGCCGCCTTCTTAGCCGCC CCGTCGCCGCCTCGGCCGCCGCCTCAGCCTCCGCCGCCGCCACCAGAGCCGCCTTCTTAGCCGCC T C ABHD8 Ensembl:ENSG00000127220 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17309549..17309830 26863196 MeRIP-seq:(Medium) rs750156546 Functional Loss SNV dbSNP153 33..33 33 - - - 55242 RMVar_ID_55242 Human_SNP_ID_660143298 m1A Human chr19 - 17314330 17314330 17314330 GCAGGTAGACTGAGGGCCGTCGGTTCTGCAGGAGGGTTGAGAAGGGGTGGGTTAGGAGAGTGCAT GCAGGTAGACTGAGGGCCGTCGGTTCTGCAGGGGGGTTGAGAAGGGGTGGGTTAGGAGAGTGCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr19:17314326..17314400;chr19:17314326..17314375 26863196,32194978 MeRIP-seq:(Medium) rs1436513515 Functional Loss SNV dbSNP153 33..33 33 - - - 55243 RMVar_ID_55243 Human_SNP_ID_660145455 m1A Human chr19 + 17319505 17319503 17319505 TTGCTTGAGCCCAGAAGGTTGAGGCTGTCCGAAAAAAAAGACTCACAGCCCCTCTCTTTTCCCTG TTGCTTGAGCCCAGAAGGTTGAGGCTGTCCG__AAAAAAGACTCACAGCCCCTCTCTTTTCCCTG GAA G DDA1 Ensembl:ENSG00000130311 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17319503..17319775 26863196 MeRIP-seq:(Medium) rs34681934 Functional Loss DEL dbSNP153 32..33 33 - - - 55244 RMVar_ID_55244 Human_SNP_ID_660145456 m1A Human chr19 + 17319505 17319503 17319505 TTGCTTGAGCCCAGAAGGTTGAGGCTGTCCGAAAAAAAAGACTCACAGCCCCTCTCTTTTCCCTG TTGCTTGAGCCCAGAAGGTTGAGGCTGTCCGA_AAAAAAGACTCACAGCCCCTCTCTTTTCCCTG GAA GA DDA1 Ensembl:ENSG00000130311 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17319503..17319775 26863196 MeRIP-seq:(Medium) rs34681934 Functional Loss DEL dbSNP153 33..33 33 - - - 55245 RMVar_ID_55245 Human_SNP_ID_660146159 m1A Human chr19 + 17322035 17322035 17322035 GGTGTCCATCTGTGAATGACTGAGATGGTGGGACTTCAGCTTCCAAGGCCAGGGGCCAGAGTGGG GGTGTCCATCTGTGAATGACTGAGATGGTGGGGCTTCAGCTTCCAAGGCCAGGGGCCAGAGTGGG A G DDA1 Ensembl:ENSG00000130311 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17321985..17322117 32194978 MeRIP-seq:(Medium) rs1456453601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013641,Human_RBP_ID_1556294,Human_RBP_ID_6726001,Human_RBP_ID_8479438,Human_RBP_ID_13392045,Human_RBP_ID_18440735,Human_RBP_ID_18724271,Human_RBP_ID_26472207 55246 RMVar_ID_55246 Human_SNP_ID_660146575 m1A Human chr19 + 17323494 17323490 17323495 CGCCCCTGTGAATGACTGATATTGCATATGAGAAGAGAAGGCAGGGCGGGTAGAGCTAATGCCAG CGCCCCTGTGAATGACTGATATTGCATAT_____GAGAAGGCAGGGCGGGTAGAGCTAATGCCAG TGAGAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17323445..17325048 26863196 MeRIP-seq:(Medium) rs746998081 Functional Loss DEL dbSNP153 30..34 33 - - - 55247 RMVar_ID_55247 Human_SNP_ID_660146578 m1A Human chr19 + 17323494 17323493 17323495 CGCCCCTGTGAATGACTGATATTGCATATGAGAAGAGAAGGCAGGGCGGGTAGAGCTAATGCCAG CGCCCCTGTGAATGACTGATATTGCATATGAG__GAGAAGGCAGGGCGGGTAGAGCTAATGCCAG GAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17323445..17325048 26863196 MeRIP-seq:(Medium) rs770827173 Functional Loss DEL dbSNP153 33..34 33 - - - 55248 RMVar_ID_55248 Human_SNP_ID_660146579 m1A Human chr19 + 17323494 17323494 17323494 CGCCCCTGTGAATGACTGATATTGCATATGAGAAGAGAAGGCAGGGCGGGTAGAGCTAATGCCAG CGCCCCTGTGAATGACTGATATTGCATATGAGGAGAGAAGGCAGGGCGGGTAGAGCTAATGCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17323445..17325048 26863196 MeRIP-seq:(Medium) rs764813369 Functional Loss SNV dbSNP153 33..33 33 - - - 55249 RMVar_ID_55249 Human_SNP_ID_660147200 m1A Human chr19 - 17325301 17325301 17325301 GGAGGAGGAGGAGCGACAGCGCCATGCAGAGCACCATGCCCGGCGGGAGCATGATTCTGGTGGCC GGAGGAGGAGGAGCGACAGCGCCATGCAGAGCCCCATGCCCGGCGGGAGCATGATTCTGGTGGCC T G ANO8 Ensembl:ENSG00000074855 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17325251..17325400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18997095 Human_Splice_Rec_1976502,Human_Splice_Rec_1976534 RMVar_hsa_circ_102865,RMVar_hsa_circ_193306 55250 RMVar_ID_55250 Human_SNP_ID_660148258 m1A Human chr19 + 17328478 17328478 17328478 CCTTCTCCACCATAGTGGGGCTCCCTTCCTCCAGGAGGGCCTCCGGGCTTGGGCCGGGCCGACGC CCTTCTCCACCATAGTGGGGCTCCCTTCCTCCGGGAGGGCCTCCGGGCTTGGGCCGGGCCGACGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17328476..17328845 26863196 MeRIP-seq:(Medium) rs1256619478 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 55251 RMVar_ID_55251 Human_SNP_ID_660148312 m1A Human chr19 + 17328560 17328560 17328560 AGCGAAGCTGACCTTCTTCAGCCGGAGCCCGCAGTCCAGGAGGCCCCCTTCCTCGCCCTCCTCCT AGCGAAGCTGACCTTCTTCAGCCGGAGCCCGCGGTCCAGGAGGCCCCCTTCCTCGCCCTCCTCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17328236..17328675 26863196 MeRIP-seq:(Medium) rs956000085 Functional Loss SNV dbSNP153 33..33 33 - - - 55252 RMVar_ID_55252 Human_SNP_ID_660148313 m1A Human chr19 + 17328560 17328560 17328560 AGCGAAGCTGACCTTCTTCAGCCGGAGCCCGCAGTCCAGGAGGCCCCCTTCCTCGCCCTCCTCCT AGCGAAGCTGACCTTCTTCAGCCGGAGCCCGCTGTCCAGGAGGCCCCCTTCCTCGCCCTCCTCCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17328236..17328675 26863196 MeRIP-seq:(Medium) rs956000085 Functional Loss SNV dbSNP153 33..33 33 - - - 55253 RMVar_ID_55253 Human_SNP_ID_660148332 m1A Human chr19 - 17328589 17328589 17328589 GGAGGAGGACGAGGAGGAAGAGGAGGACGAGGAGGAGGGCGAGGAAGGGGGCCTCCTGGACTGCG GGAGGAGGACGAGGAGGAAGAGGAGGACGAGGGGGAGGGCGAGGAAGGGGGCCTCCTGGACTGCG T C ANO8 Ensembl:ENSG00000074855 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17327665..17328700 26863196 MeRIP-seq:(Medium) rs775012307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263219,Human_RBP_ID_909473,Human_RBP_ID_3954693,Human_RBP_ID_5650850,Human_RBP_ID_8233439,Human_RBP_ID_18997098,Human_RBP_ID_19089631,Human_RBP_ID_21977783,Human_RBP_ID_22977436,Human_RBP_ID_26336005 RMVar_hsa_circ_16443,RMVar_hsa_circ_99468,RMVar_hsa_circ_193307,RMVar_hsa_circ_57988 55254 RMVar_ID_55254 Human_SNP_ID_660149051 m1A Human chr19 - 17330359 17330359 17330359 CTGTGTCTTCTTGCTCATGCTTGGCTGCTTCCAGCTGCAGGTGACCCCCCATACCCTCACCCGCC CTGTGTCTTCTTGCTCATGCTTGGCTGCTTCCCGCTGCAGGTGACCCCCCATACCCTCACCCGCC T G ANO8 Ensembl:ENSG00000074855 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17329530..17330904 32194978 MeRIP-seq:(Medium) rs1228975008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27815313 Human_Splice_Rec_1976487,Human_Splice_Rec_1976519,Human_Splice_Rec_1976551 RMVar_hsa_circ_16443,RMVar_hsa_circ_82242,RMVar_hsa_circ_99468,RMVar_hsa_circ_193307,RMVar_hsa_circ_57988,RMVar_hsa_circ_193309 55255 RMVar_ID_55255 Human_SNP_ID_660150135 m1A Human chr19 - 17333425 17333425 17333425 TGCCTACGCCTTCTTTGTCACCGCCACGTATGAGAGGCGAGTCCCCTGTCCCTGGCCTCTCGCTG TGCCTACGCCTTCTTTGTCACCGCCACGTATGCGAGGCGAGTCCCCTGTCCCTGGCCTCTCGCTG T G ANO8 Ensembl:ENSG00000074855 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17333417..17333617 32194978 MeRIP-seq:(Medium) rs370283813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18997102 RMVar_hsa_circ_82242,RMVar_hsa_circ_193309 55256 RMVar_ID_55256 Human_SNP_ID_660150546 m1A Human chr19 + 17334620 17334620 17334620 GCAGGCTCGCCCTCCGGCGGGGGCCTCTTGCCACGCTCGCCCTCCAGGGACGTGCCCCCGGCGCC GCAGGCTCGCCCTCCGGCGGGGGCCTCTTGCCCCGCTCGCCCTCCAGGGACGTGCCCCCGGCGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17334376..17334829 26863196 MeRIP-seq:(Medium) rs1476546524 Functional Loss SNV dbSNP153 33..33 33 - - - 55257 RMVar_ID_55257 Human_SNP_ID_660151534 m1A Human chr19 + 17337663 17337653 17337663 CCCTGGCGGCCCAAGCGGCACGTGGGCCTCGCAGGTGGGGCTACAGGGGAAGGGGTGCGACAGCT CCCTGGCGGCCCAAGCGGCACGT__________GGTGGGGCTACAGGGGAAGGGGTGCGACAGCT TGGGCCTCGCA T GTPBP3 Ensembl:ENSG00000130299 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:17337576..17337728 26863410 MeRIP-seq:(Medium) rs1303801792 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_241573,Human_RBP_ID_279292,Human_RBP_ID_773878,Human_RBP_ID_909477,Human_RBP_ID_4558208,Human_RBP_ID_19089635,Human_RBP_ID_22448500,Human_RBP_ID_23786143,Human_RBP_ID_26985140 Human_Splice_Rec_1976623,Human_Splice_Rec_1976625,Human_Splice_Rec_1976639,Human_Splice_Rec_1976651,Human_Splice_Rec_1976671,Human_Splice_Rec_1976681,Human_Splice_Rec_1976701,Human_Splice_Rec_1976711,Human_Splice_Rec_1976721 55258 RMVar_ID_55258 Human_SNP_ID_660151776 m1A Human chr19 + 17338155 17338155 17338155 GCCAGCGGCCACGCCCTCCGAATTCTCACAGCACCCCGAGACCTGCCCCTTGCTCGCCACGCCAG GCCAGCGGCCACGCCCTCCGAATTCTCACAGCGCCCCGAGACCTGCCCCTTGCTCGCCACGCCAG A G GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:17338054..17338200 26863196 MeRIP-seq:(Medium) rs756583525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4509160,Human_RBP_ID_9329893 RMVar_hsa_circ_268493 55259 RMVar_ID_55259 Human_SNP_ID_660151825 m1A Human chr19 - 17338249 17338249 17338249 GAGGCTCGGAACCTGGGGACCCTCACCTGGGAACCAGAGCACCAGTGCGCGGTCCAGAGGCTCCC GAGGCTCGGAACCTGGGGACCCTCACCTGGGAGCCAGAGCACCAGTGCGCGGTCCAGAGGCTCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17338075..17338275 32194978 MeRIP-seq:(Medium) rs747176659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119787,RMVar_hsa_circ_193310 55260 RMVar_ID_55260 Human_SNP_ID_660151987 m1A Human chr19 + 17338575 17338575 17338575 CGTGCCAGGGCTTCGACCGGCGGAGGCAGGCGAGTTCACCAGACGGGCGTTCGCCAATGGGAAGC CGTGCCAGGGCTTCGACCGGCGGAGGCAGGCGTGTTCACCAGACGGGCGTTCGCCAATGGGAAGC A T GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17338452..17338679 26863196 MeRIP-seq:(Medium) rs1232775917 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_515722,Human_RBP_ID_909479,Human_RBP_ID_1556318,Human_RBP_ID_6726065,Human_RBP_ID_9382283,Human_RBP_ID_18994580,Human_RBP_ID_22446542,Human_RBP_ID_23257741,Human_RBP_ID_26336008 Human_Splice_Rec_1976566,Human_Splice_Rec_1976582,Human_Splice_Rec_1976590,Human_Splice_Rec_1976594,Human_Splice_Rec_1976610,Human_Splice_Rec_1976616,Human_Splice_Rec_1976622,Human_Splice_Rec_1976630,Human_Splice_Rec_1976644,Human_Splice_Rec_1976656,Human_Splice_Rec_1976666,Human_Splice_Rec_1976670,Human_Splice_Rec_1976676,Human_Splice_Rec_1976686,Human_Splice_Rec_1976694,Human_Splice_Rec_1976698,Human_Splice_Rec_1976706,Human_Splice_Rec_1976716,Human_Splice_Rec_1976726 RMVar_hsa_circ_268493 55261 RMVar_ID_55261 Human_SNP_ID_660152033 m1A Human chr19 + 17338657 17338656 17338658 GAGGGGCTGGCGGACCTTATCCACGCGGAAACAGAGGCGCAGCGGCGGCAGGCCCTCAGGCAGCT GAGGGGCTGGCGGACCTTATCCACGCGGAAAC__AGGCGCAGCGGCGGCAGGCCCTCAGGCAGCT CAG C GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr19:17337926..17338775;chr19:17338351..17338750;chr19:17338526..17338758 26863196 MeRIP-seq:(Medium) rs1414881768 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_241576,Human_RBP_ID_9380790,Human_RBP_ID_22977437 RMVar_hsa_circ_268493 55262 RMVar_ID_55262 Human_SNP_ID_660152295 m1A Human chr19 + 17339202 17339202 17339202 CGAGATGCCAGGCGCGGGCAGAGGCTCCGCTCAGGGGTGCACGTAGTGGTCACTGGACCCCCCAA CGAGATGCCAGGCGCGGGCAGAGGCTCCGCTCCGGGGTGCACGTAGTGGTCACTGGACCCCCCAA A C GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17339151..17339292 26863196 MeRIP-seq:(Medium) rs554038809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515725,Human_RBP_ID_1013650,Human_RBP_ID_13392173,Human_RBP_ID_18994583,Human_RBP_ID_22501888,Human_RBP_ID_23114809 Human_Splice_Rec_1976568,Human_Splice_Rec_1976569,Human_Splice_Rec_1976595,Human_Splice_Rec_1976632,Human_Splice_Rec_1976633,Human_Splice_Rec_1976645,Human_Splice_Rec_1976658,Human_Splice_Rec_1976659,Human_Splice_Rec_1976678,Human_Splice_Rec_1976679,Human_Splice_Rec_1976687,Human_Splice_Rec_1976700,Human_Splice_Rec_1976708,Human_Splice_Rec_1976709,Human_Splice_Rec_1976717,Human_Splice_Rec_1976728,Human_Splice_Rec_1976729,Human_Splice_Rec_1976733 RMVar_hsa_circ_106899,RMVar_hsa_circ_193311 55263 RMVar_ID_55263 Human_SNP_ID_660152296 m1A Human chr19 + 17339202 17339202 17339202 CGAGATGCCAGGCGCGGGCAGAGGCTCCGCTCAGGGGTGCACGTAGTGGTCACTGGACCCCCCAA CGAGATGCCAGGCGCGGGCAGAGGCTCCGCTCGGGGGTGCACGTAGTGGTCACTGGACCCCCCAA A G GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17339151..17339292 26863196 MeRIP-seq:(Medium) rs554038809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515725,Human_RBP_ID_1013650,Human_RBP_ID_13392173,Human_RBP_ID_18994583,Human_RBP_ID_22501888,Human_RBP_ID_23114809 Human_Splice_Rec_1976568,Human_Splice_Rec_1976569,Human_Splice_Rec_1976595,Human_Splice_Rec_1976632,Human_Splice_Rec_1976633,Human_Splice_Rec_1976645,Human_Splice_Rec_1976658,Human_Splice_Rec_1976659,Human_Splice_Rec_1976678,Human_Splice_Rec_1976679,Human_Splice_Rec_1976687,Human_Splice_Rec_1976700,Human_Splice_Rec_1976708,Human_Splice_Rec_1976709,Human_Splice_Rec_1976717,Human_Splice_Rec_1976728,Human_Splice_Rec_1976729,Human_Splice_Rec_1976733 RMVar_hsa_circ_106899,RMVar_hsa_circ_193311 55264 RMVar_ID_55264 Human_SNP_ID_660152815 m1A Human chr19 + 17340378 17340378 17340378 GTTCTGATTAAGTCCTGCCCCCGGCCCTCCGGACATGTTTCTCATCCCTAAGCCCTCCGCCCAGC GTTCTGATTAAGTCCTGCCCCCGGCCCTCCGGGCATGTTTCTCATCCCTAAGCCCTCCGCCCAGC A G GTPBP3 Ensembl:ENSG00000130299 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:17340365..17340805;chr19:17340374..17340819 26863196 MeRIP-seq:(Medium) rs11666309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1187732,Human_RBP_ID_13392209 RMVar_hsa_circ_106899,RMVar_hsa_circ_193311 55265 RMVar_ID_55265 Human_SNP_ID_660153333 m1A Human chr19 - 17341689 17341689 17341689 CGACTTCCCTGGATCCCGTCACTTGCCCACACAGAAGTCCTGGAAGATGATGTCCAGGATCTCCT CGACTTCCCTGGATCCCGTCACTTGCCCACACTGAAGTCCTGGAAGATGATGTCCAGGATCTCCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17341639..17341789 32194978 MeRIP-seq:(Medium) rs1279809281 Functional Loss SNV dbSNP153 33..33 33 - - - 55266 RMVar_ID_55266 Human_SNP_ID_660168845 m1A Human chr19 - 17395367 17395367 17395367 GGCCCTGCGATGGGAATGCACTTGGTGGAAGAACCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA GGCCCTGCGATGGGAATGCACTTGGTGGAAGATCCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:17395250..17395453;chr19:17395001..17395549 26863196 MeRIP-seq:(Medium) rs8106139 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6618,GWAS_ID_6619,GWAS_ID_6620,GWAS_ID_6621,GWAS_ID_6622,GWAS_ID_6623,GWAS_ID_6624 55267 RMVar_ID_55267 Human_SNP_ID_660168846 m1A Human chr19 - 17395367 17395367 17395367 GGCCCTGCGATGGGAATGCACTTGGTGGAAGAACCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA GGCCCTGCGATGGGAATGCACTTGGTGGAAGAGCCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:17395250..17395453;chr19:17395001..17395549 26863196 MeRIP-seq:(Medium) rs8106139 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6618,GWAS_ID_6619,GWAS_ID_6620,GWAS_ID_6621,GWAS_ID_6622,GWAS_ID_6623,GWAS_ID_6624 55268 RMVar_ID_55268 Human_SNP_ID_660170982 m1A Human chr19 + 17403022 17403022 17403022 CCCAGAAAAAAGCAACCCCCCCCGCAAAAAAAACCCATAACAACAGGCAGCACATGCCCCCCACA CCCAGAAAAAAGCAACCCCCCCCGCAAAAAAACCCCATAACAACAGGCAGCACATGCCCCCCACA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17403001..17403025 26863196 MeRIP-seq:(Medium) rs539156169 Functional Loss SNV dbSNP153 33..33 33 - - - 55269 RMVar_ID_55269 Human_SNP_ID_660171249 m1A Human chr19 - 17403813 17403813 17403813 GATTTGCCATCTGTACCGCAGAAGAGAAAACCAGGTCTTAAGCGTGAGAATCGCGGACAAGAAGT GATTTGCCATCTGTACCGCAGAAGAGAAAACCGGGTCTTAAGCGTGAGAATCGCGGACAAGAAGT T C BST2 Ensembl:ENSG00000130303 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:17403538..17403855;chr19:17403536..17403858 26863196 MeRIP-seq:(Medium) rs1330531655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53912,Human_RBP_ID_2558918,Human_RBP_ID_18997115,Human_RBP_ID_22665103,Human_RBP_ID_27157342 Human_Splice_Rec_1976770,Human_Splice_Rec_1976776,Human_Splice_Rec_1976782 RMVar_hsa_circ_107036,RMVar_hsa_circ_123645,RMVar_hsa_circ_193316,RMVar_hsa_circ_90426,RMVar_hsa_circ_99769,RMVar_hsa_circ_193317,RMVar_hsa_circ_193314,RMVar_hsa_circ_193315 55270 RMVar_ID_55270 Human_SNP_ID_660171771 m1A Human chr19 - 17405575 17405575 17405575 ACTCCAGGCCAGACTCTAAAGGGGAGATCTGGATGGCATCTACTTCGTATGACTATTGCAGAGTG ACTCCAGGCCAGACTCTAAAGGGGAGATCTGGTTGGCATCTACTTCGTATGACTATTGCAGAGTG T A BST2 Ensembl:ENSG00000130303 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17405526..17405600 26863196 MeRIP-seq:(Medium) rs1329664881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55307,Human_RBP_ID_4558210 RMVar_hsa_circ_107036,RMVar_hsa_circ_193317 55271 RMVar_ID_55271 Human_SNP_ID_660176076 m1A Human chr19 - 17420227 17420227 17420227 CCCCATTCGACCCCCGCCCCTCGACGCCGCTCACCGCGCTGAACCCCCGCGGCGGGGGTGCAGAG CCCCATTCGACCCCCGCCCCTCGACGCCGCTCGCCGCGCTGAACCCCCGCGGCGGGGGTGCAGAG T C AC010319.4 Ensembl:ENSG00000269481 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:17420152..17420297 26863410 MeRIP-seq:(Medium) rs771212419 Functional Loss SNV dbSNP153 33..33 33 - - - 55272 RMVar_ID_55272 Human_SNP_ID_660177443 m1A Human chr19 + 17424602 17424602 17424602 GGGGTTTCAGGTTGAGATCGGGCCCAAGGCTGACCCACCTCTGCCCGCCAGGCCTTCTCTGCTTT GGGGTTTCAGGTTGAGATCGGGCCCAAGGCTGTCCCACCTCTGCCCGCCAGGCCTTCTCTGCTTT A T MVB12A Ensembl:ENSG00000141971 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:17424601..17424700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1976909,Human_Splice_Rec_1976949,Human_Splice_Rec_1976997,Human_Splice_Rec_1977013 RMVar_hsa_circ_54762 55273 RMVar_ID_55273 Human_SNP_ID_660177623 m1A Human chr19 + 17425013 17425011 17425013 CAGCGTCTCATAGTCCCTCACCCTTCCGCGGAAAGAGCCCCCTTACTCCACCTCCCCGCCAGCCT CAGCGTCTCATAGTCCCTCACCCTTCCGCGG__AGAGCCCCCTTACTCCACCTCCCCGCCAGCCT GAA G MVB12A Ensembl:ENSG00000141971 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17424906..17425075 26863196 MeRIP-seq:(Medium) rs1293896766 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_515773,Human_RBP_ID_5116779,Human_RBP_ID_5145704,Human_RBP_ID_17386746,Human_RBP_ID_22446545,Human_RBP_ID_26817194 Human_Splice_Rec_1976910,Human_Splice_Rec_1976950,Human_Splice_Rec_1976998,Human_Splice_Rec_1977014,Human_Splice_Rec_1977022 RMVar_hsa_circ_77474,RMVar_hsa_circ_110080,RMVar_hsa_circ_193320,RMVar_hsa_circ_193321 55274 RMVar_ID_55274 Human_SNP_ID_660177633 m1A Human chr19 + 17425030 17425030 17425030 TCACCCTTCCGCGGAAAGAGCCCCCTTACTCCACCTCCCCGCCAGCCTGGGGCCACCCCCCCTCA TCACCCTTCCGCGGAAAGAGCCCCCTTACTCCCCCTCCCCGCCAGCCTGGGGCCACCCCCCCTCA A C MVB12A Ensembl:ENSG00000141971 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17424926..17425290 26863196 MeRIP-seq:(Medium) rs776799800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515773,Human_RBP_ID_5116779,Human_RBP_ID_17386746,Human_RBP_ID_22446545,Human_RBP_ID_26817194 Human_Splice_Rec_1976910,Human_Splice_Rec_1976950,Human_Splice_Rec_1976998,Human_Splice_Rec_1977014,Human_Splice_Rec_1977022 Human_miRNA_ID_2147375,Human_miRNA_ID_2988801,Human_miRNA_ID_3022502 RMVar_hsa_circ_77474,RMVar_hsa_circ_110080,RMVar_hsa_circ_193320,RMVar_hsa_circ_193321 55275 RMVar_ID_55275 Human_SNP_ID_660195471 m1A Human chr19 + 17486912 17486912 17486912 TGCGGCGCGAGCCCCTGGCCTTCTGCCTGGGCACCTCGGGCGCTAAGGCCCTGATCTTTGGAGGA TGCGGCGCGAGCCCCTGGCCTTCTGCCTGGGCTCCTCGGGCGCTAAGGCCCTGATCTTTGGAGGA A T SLC27A1 Ensembl:ENSG00000130304 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17486881..17487164 26863196 MeRIP-seq:(Medium) rs1568415713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22763943 Human_Splice_Rec_1977051,Human_Splice_Rec_1977071 55276 RMVar_ID_55276 Human_SNP_ID_660200977 m1A Human chr19 + 17504766 17504766 17504766 GCCCATCCTGGACTGAGAAACTGGAACCTCAGAGGAACCCGTGCCTCTCTGCTGCCTTGGTGCCC GCCCATCCTGGACTGAGAAACTGGAACCTCAGGGGAACCCGTGCCTCTCTGCTGCCTTGGTGCCC A G SLC27A1 Ensembl:ENSG00000130304 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17504717..17504868 32194978 MeRIP-seq:(Medium) rs1467011384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2491775 RMVar_hsa_circ_111506,RMVar_hsa_circ_193324 55277 RMVar_ID_55277 Human_SNP_ID_660201011 m1A Human chr19 - 17504841 17504841 17504841 GAAGAGTTAAGGCCAGACAGGGACAGGGATGGAAGGAGACAGAGGCTGAAAAGCAGGGAGAGGAG GAAGAGTTAAGGCCAGACAGGGACAGGGATGGGAGGAGACAGAGGCTGAAAAGCAGGGAGAGGAG T C AC010618.3 Ensembl:ENSG00000269439 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17504790..17504913 26863196 MeRIP-seq:(Medium) rs1165222802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587328 55278 RMVar_ID_55278 Human_SNP_ID_660201319 m1A Human chr19 + 17505875 17505875 17505875 TGAATATACCCCACCTGGTGGTGGCCCCTCCGATGTCCCCACTGATGGCTCTGACACCGTGTTGG TGAATATACCCCACCTGGTGGTGGCCCCTCCGGTGTCCCCACTGATGGCTCTGACACCGTGTTGG A G SLC27A1 Ensembl:ENSG00000130304 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17505617..17505968 32194978 MeRIP-seq:(Medium) rs1238390642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2726600,Human_miRNA_ID_2769359 RMVar_hsa_circ_111506,RMVar_hsa_circ_193324 55279 RMVar_ID_55279 Human_SNP_ID_660201702 m1A Human chr19 + 17507062 17507062 17507062 TGTCCTCTTCCATGTACAGGCCGGCTGGTGTGAGAGCTCTGGGTGAAAGTCGCTAGGCCTGCTGG TGTCCTCTTCCATGTACAGGCCGGCTGGTGTGTGAGCTCTGGGTGAAAGTCGCTAGGCCTGCTGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17506979..17507231 26863196 MeRIP-seq:(Medium) rs1275441392 Functional Loss SNV dbSNP153 33..33 33 - - - 55280 RMVar_ID_55280 Human_SNP_ID_660201710 m1A Human chr19 - 17507079 17507079 17507079 CAGCTCAGACGGCCACCCCAGCAGGCCTAGCGACTTTCACCCAGAGCTCTCACACCAGCCGGCCT CAGCTCAGACGGCCACCCCAGCAGGCCTAGCGGCTTTCACCCAGAGCTCTCACACCAGCCGGCCT T C AC010618.3 Ensembl:ENSG00000269439 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17506882..17507235 26863196 MeRIP-seq:(Medium) rs1293101589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587332 55281 RMVar_ID_55281 Human_SNP_ID_660203274 m1A Human chr19 + 17511943 17511943 17511943 AGCGCCTCGTGCCCTTCGATCACGCCGAGAGCACGTACGGCCTCTACCGGGTGAGAGCTACGGGG AGCGCCTCGTGCCCTTCGATCACGCCGAGAGCGCGTACGGCCTCTACCGGGTGAGAGCTACGGGG A G PGLS Ensembl:ENSG00000130313 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17511691..17511979 32194978 MeRIP-seq:(Medium) rs1467239607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19089653 Human_Splice_Rec_1977145,Human_Splice_Rec_1977155,Human_Splice_Rec_1977163,Human_Splice_Rec_1977171 RMVar_hsa_circ_193325,RMVar_hsa_circ_80786 55282 RMVar_ID_55282 Human_SNP_ID_660203842 m1A Human chr19 - 17513832 17513832 17513832 ACTCCCTATTCCCTAGCACTCTGCAGCATTTCACAATTATTTATTTTGAGACAGAGTCTCAACTG ACTCCCTATTCCCTAGCACTCTGCAGCATTTCCCAATTATTTATTTTGAGACAGAGTCTCAACTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17513830..17513971 26863196 MeRIP-seq:(Medium) rs75664063 Functional Loss SNV dbSNP153 33..33 33 - - - 55283 RMVar_ID_55283 Human_SNP_ID_660204972 m1A Human chr19 - 17517702 17517702 17517702 TGGGAGCCACAATCTTCTCCCGCTCCTTGGGGAGGAAGCCCAGGGATGGAGGCAGAAGGACAATG TGGGAGCCACAATCTTCTCCCGCTCCTTGGGGGGGAAGCCCAGGGATGGAGGCAGAAGGACAATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17517701..17517725 26863196 MeRIP-seq:(Medium) rs1198638334 Functional Loss SNV dbSNP153 33..33 33 - - - 55284 RMVar_ID_55284 Human_SNP_ID_660204999 m1A Human chr19 + 17517762 17517762 17517762 TCCCATCAGTGACTCCCCGAAGCCACCGCCACAGCGTGTGACCCTCACACTACCTGTCCTGAATG TCCCATCAGTGACTCCCCGAAGCCACCGCCACGGCGTGTGACCCTCACACTACCTGTCCTGAATG A G PGLS Ensembl:ENSG00000130313 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17517710..17517826 26863196 MeRIP-seq:(Medium) rs773593679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9084952,Human_RBP_ID_18192086,Human_RBP_ID_26815488 Human_Splice_Rec_1977152,Human_Splice_Rec_1977153,Human_Splice_Rec_1977160,Human_Splice_Rec_1977161,Human_Splice_Rec_1977170,Human_Splice_Rec_1977180,Human_Splice_Rec_1977181 Human_miRNA_ID_2061770 RMVar_hsa_circ_193325,RMVar_hsa_circ_80786,RMVar_hsa_circ_295626,RMVar_hsa_circ_193329,RMVar_hsa_circ_92242,RMVar_hsa_circ_193328,RMVar_hsa_circ_321938,RMVar_hsa_circ_193330,RMVar_hsa_circ_78216 55285 RMVar_ID_55285 Human_SNP_ID_660205007 m1A Human chr19 + 17517778 17517778 17517778 CCGAAGCCACCGCCACAGCGTGTGACCCTCACACTACCTGTCCTGAATGCAGCACGAACTGTCAT CCGAAGCCACCGCCACAGCGTGTGACCCTCACGCTACCTGTCCTGAATGCAGCACGAACTGTCAT A G PGLS Ensembl:ENSG00000130313 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6743 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18192086,Human_RBP_ID_26817200 Human_Splice_Rec_1977152,Human_Splice_Rec_1977153,Human_Splice_Rec_1977160,Human_Splice_Rec_1977161,Human_Splice_Rec_1977170,Human_Splice_Rec_1977180,Human_Splice_Rec_1977181 Human_miRNA_ID_2061770,Human_miRNA_ID_2168887,Human_miRNA_ID_2170410,Human_miRNA_ID_2627676,Human_miRNA_ID_2748512,Human_miRNA_ID_2766094 RMVar_hsa_circ_193325,RMVar_hsa_circ_80786,RMVar_hsa_circ_295626,RMVar_hsa_circ_193329,RMVar_hsa_circ_92242,RMVar_hsa_circ_193328,RMVar_hsa_circ_321938,RMVar_hsa_circ_193330,RMVar_hsa_circ_78216 55286 RMVar_ID_55286 Human_SNP_ID_660205008 m1A Human chr19 + 17517778 17517778 17517778 CCGAAGCCACCGCCACAGCGTGTGACCCTCACACTACCTGTCCTGAATGCAGCACGAACTGTCAT CCGAAGCCACCGCCACAGCGTGTGACCCTCACTCTACCTGTCCTGAATGCAGCACGAACTGTCAT A T PGLS Ensembl:ENSG00000130313 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18192086,Human_RBP_ID_26817200 Human_Splice_Rec_1977152,Human_Splice_Rec_1977153,Human_Splice_Rec_1977160,Human_Splice_Rec_1977161,Human_Splice_Rec_1977170,Human_Splice_Rec_1977180,Human_Splice_Rec_1977181 Human_miRNA_ID_2061770,Human_miRNA_ID_2168887,Human_miRNA_ID_2170410,Human_miRNA_ID_2627676,Human_miRNA_ID_2748512,Human_miRNA_ID_2766094 RMVar_hsa_circ_193325,RMVar_hsa_circ_80786,RMVar_hsa_circ_295626,RMVar_hsa_circ_193329,RMVar_hsa_circ_92242,RMVar_hsa_circ_193328,RMVar_hsa_circ_321938,RMVar_hsa_circ_193330,RMVar_hsa_circ_78216 55287 RMVar_ID_55287 Human_SNP_ID_660215978 m1A Human chr19 + 17555832 17555832 17555832 GGCCCCGCCGGGCGCCGACGCCTACTTCCCCGAGGAGCGCTGGAGCCCGGAGTCGCCCCTGCAGG GGCCCCGCCGGGCGCCGACGCCTACTTCCCCGGGGAGCGCTGGAGCCCGGAGTCGCCCCTGCAGG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17555626..17556020 26863196 MeRIP-seq:(Medium) rs978458440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53914,Human_RBP_ID_240219,Human_RBP_ID_826805,Human_RBP_ID_4557333,Human_RBP_ID_9328779,Human_RBP_ID_18470538,Human_RBP_ID_22069980,Human_RBP_ID_22447544 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 55288 RMVar_ID_55288 Human_SNP_ID_660218003 m1A Human chr19 + 17562767 17562767 17562767 GCCTGCATGGGGTGGGGGCCGTGGAGAAAGGCAGGGGGTTCAGGATGCGTCACGAGGTGAAGGAG GCCTGCATGGGGTGGGGGCCGTGGAGAAAGGCGGGGGGTTCAGGATGCGTCACGAGGTGAAGGAG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17562763..17562852 26863196 MeRIP-seq:(Medium) rs968427842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33195,RMVar_hsa_circ_107345,RMVar_hsa_circ_327617,RMVar_hsa_circ_193333,RMVar_hsa_circ_376746,RMVar_hsa_circ_282270,RMVar_hsa_circ_108912,RMVar_hsa_circ_193335,RMVar_hsa_circ_193336,RMVar_hsa_circ_193337,RMVar_hsa_circ_109761,RMVar_hsa_circ_112646,RMVar_hsa_circ_193339,RMVar_hsa_circ_193340 55289 RMVar_ID_55289 Human_SNP_ID_660219538 m1A Human chr19 + 17568473 17568473 17568473 CCACTATCACGGGTCTCCATCCTCACCTTTCAAGACCCCTACGCGGAACTCTCGCTCTCTCCCCA CCACTATCACGGGTCTCCATCCTCACCTTTCAGGACCCCTACGCGGAACTCTCGCTCTCTCCCCA A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17568469..17568619 26863196 MeRIP-seq:(Medium) rs772952841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107345,RMVar_hsa_circ_327617,RMVar_hsa_circ_193333,RMVar_hsa_circ_376746,RMVar_hsa_circ_282270,RMVar_hsa_circ_108912,RMVar_hsa_circ_193335,RMVar_hsa_circ_193336,RMVar_hsa_circ_193337,RMVar_hsa_circ_109761,RMVar_hsa_circ_112646,RMVar_hsa_circ_193339,RMVar_hsa_circ_193340,RMVar_hsa_circ_298867,RMVar_hsa_circ_346199,RMVar_hsa_circ_84312,RMVar_hsa_circ_193341 55290 RMVar_ID_55290 Human_SNP_ID_660221625 m1A Human chr19 + 17576366 17576366 17576366 CCCAGGGCATCATAGCTGAGAAGTAACGTTACAGAGCAGGGAAAGGAAGGGTATTTCAAGCAGGG CCCAGGGCATCATAGCTGAGAAGTAACGTTACGGAGCAGGGAAAGGAAGGGTATTTCAAGCAGGG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17576363..17576987 26863196 MeRIP-seq:(Medium) rs796895146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21978530 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_376746,RMVar_hsa_circ_108912,RMVar_hsa_circ_193336,RMVar_hsa_circ_193337,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_111618,RMVar_hsa_circ_193343,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346 55291 RMVar_ID_55291 Human_SNP_ID_660221641 m1A Human chr19 - 17576442 17576442 17576442 CCCCAGCCCCACCTCTATGCCCCTGCCAACCCAAAGAACCCCCATTCCTACCTCAGGGCCTTTGC CCCCAGCCCCACCTCTATGCCCCTGCCAACCCCAAGAACCCCCATTCCTACCTCAGGGCCTTTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17576440..17577027 26863196 MeRIP-seq:(Medium) rs1448749119 Functional Loss SNV dbSNP153 33..33 33 - - - 55292 RMVar_ID_55292 Human_SNP_ID_660221793 m1A Human chr19 + 17576807 17576807 17576807 GTGGCCAGGGCTGAGTGGTGCGGCTGGGGGGCAGGTTGAAGCTGTAGCCTGGGGTGTGGCCAGGG GTGGCCAGGGCTGAGTGGTGCGGCTGGGGGGCGGGTTGAAGCTGTAGCCTGGGGTGTGGCCAGGG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:17576797..17576918 26863196 MeRIP-seq:(Medium) rs1409047448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21977803 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_376746,RMVar_hsa_circ_108912,RMVar_hsa_circ_193336,RMVar_hsa_circ_193337,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_111618,RMVar_hsa_circ_193343,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346 55293 RMVar_ID_55293 Human_SNP_ID_660221819 m1A Human chr19 + 17576890 17576890 17576890 GGCAGGGTGAGGCTGGGACCTGGGGCGAGTCCAGGGTTGAGTAGCGGGGCCTTGGGCGCGGTGAA GGCAGGGTGAGGCTGGGACCTGGGGCGAGTCCGGGGTTGAGTAGCGGGGCCTTGGGCGCGGTGAA A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17576888..17576965 26863196 MeRIP-seq:(Medium) rs577809668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9427146,Human_RBP_ID_21978532 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_376746,RMVar_hsa_circ_108912,RMVar_hsa_circ_193336,RMVar_hsa_circ_193337,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_111618,RMVar_hsa_circ_193343,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346 55294 RMVar_ID_55294 Human_SNP_ID_660222784 m1A Human chr19 - 17579711 17579711 17579711 ACCCCACCTTCAAGCCCCGCCTCTAAGCCATGACCCATCCCCAGGTCCCAGCTCCACCCTGCCCC ACCCCACCTTCAAGCCCCGCCTCTAAGCCATGGCCCATCCCCAGGTCCCAGCTCCACCCTGCCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17579706..17579885 26863196 MeRIP-seq:(Medium) rs1244813742 Functional Loss SNV dbSNP153 33..33 33 - - - 55295 RMVar_ID_55295 Human_SNP_ID_660223120 m1A Human chr19 + 17580800 17580800 17580800 GGAGGCCGACTATTCCTACTGGACCCTGGCCTACGTGATCTCCCTGCAAGGCGCCCGCAAACTGC GGAGGCCGACTATTCCTACTGGACCCTGGCCTGCGTGATCTCCCTGCAAGGCGCCCGCAAACTGC A G COLGALT1 Ensembl:ENSG00000130309 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17580751..17580852 26863196 MeRIP-seq:(Medium) rs1180636570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515832,Human_RBP_ID_826818,Human_RBP_ID_1881113,Human_RBP_ID_4509462,Human_RBP_ID_5261297,Human_RBP_ID_9293518,Human_RBP_ID_13392565,Human_RBP_ID_18997129,Human_RBP_ID_22967682,Human_RBP_ID_26465830,Human_RBP_ID_27465139 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_108912,RMVar_hsa_circ_193337,RMVar_hsa_circ_98019,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346,RMVar_hsa_circ_99329,RMVar_hsa_circ_193347,RMVar_hsa_circ_115879,RMVar_hsa_circ_193348,RMVar_hsa_circ_117106,RMVar_hsa_circ_193350,RMVar_hsa_circ_193352,RMVar_hsa_circ_87182,RMVar_hsa_circ_193351 55296 RMVar_ID_55296 Human_SNP_ID_660223164 m1A Human chr19 + 17580896 17580896 17580896 TGTGGACGAGTTCCTGCCCGTCATGTTCGACAAACACCCAGTGTGAGAGGGGCAGGCGGCTGCTG TGTGGACGAGTTCCTGCCCGTCATGTTCGACAGACACCCAGTGTGAGAGGGGCAGGCGGCTGCTG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17580648..17580922 26863196 MeRIP-seq:(Medium) rs759748599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146243,Human_RBP_ID_18470542 Human_Splice_Rec_1977485,Human_Splice_Rec_1977519 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_108912,RMVar_hsa_circ_193337,RMVar_hsa_circ_98019,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346,RMVar_hsa_circ_99329,RMVar_hsa_circ_193347,RMVar_hsa_circ_115879,RMVar_hsa_circ_193348,RMVar_hsa_circ_117106,RMVar_hsa_circ_193350,RMVar_hsa_circ_193352,RMVar_hsa_circ_87182,RMVar_hsa_circ_193351 55297 RMVar_ID_55297 Human_SNP_ID_660223439 m1A Human chr19 + 17581492 17581488 17581492 AAGCCAAAGCAGCCATCGGTGGCCCAGGCTCCACGTGCTTACTGAGGACATCAGGTCCACCTCTG AAGCCAAAGCAGCCATCGGTGGCCCAGGC____CGTGCTTACTGAGGACATCAGGTCCACCTCTG CTCCA C COLGALT1 Ensembl:ENSG00000130309 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17581442..17581579 26863196 MeRIP-seq:(Medium) rs751888144 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_53929,Human_RBP_ID_515840,Human_RBP_ID_6726211,Human_RBP_ID_13392587,Human_RBP_ID_17387306,Human_RBP_ID_17656876,Human_RBP_ID_17916950,Human_RBP_ID_22446549,Human_RBP_ID_27157349,Human_RBP_ID_27269914,Human_RBP_ID_27473321 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_108912,RMVar_hsa_circ_193337,RMVar_hsa_circ_98019,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346,RMVar_hsa_circ_81530,RMVar_hsa_circ_115879,RMVar_hsa_circ_193348,RMVar_hsa_circ_117106,RMVar_hsa_circ_193350,RMVar_hsa_circ_193352,RMVar_hsa_circ_193353 55298 RMVar_ID_55298 Human_SNP_ID_660223443 m1A Human chr19 + 17581492 17581492 17581492 AAGCCAAAGCAGCCATCGGTGGCCCAGGCTCCACGTGCTTACTGAGGACATCAGGTCCACCTCTG AAGCCAAAGCAGCCATCGGTGGCCCAGGCTCCGCGTGCTTACTGAGGACATCAGGTCCACCTCTG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17581442..17581579 26863196 MeRIP-seq:(Medium) rs1262815665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53929,Human_RBP_ID_515840,Human_RBP_ID_6726211,Human_RBP_ID_13392587,Human_RBP_ID_17387306,Human_RBP_ID_17656876,Human_RBP_ID_17916950,Human_RBP_ID_22446549,Human_RBP_ID_27157349,Human_RBP_ID_27269914,Human_RBP_ID_27473321 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333,RMVar_hsa_circ_108912,RMVar_hsa_circ_193337,RMVar_hsa_circ_98019,RMVar_hsa_circ_109761,RMVar_hsa_circ_193340,RMVar_hsa_circ_84312,RMVar_hsa_circ_101210,RMVar_hsa_circ_193341,RMVar_hsa_circ_193344,RMVar_hsa_circ_119079,RMVar_hsa_circ_193346,RMVar_hsa_circ_81530,RMVar_hsa_circ_115879,RMVar_hsa_circ_193348,RMVar_hsa_circ_117106,RMVar_hsa_circ_193350,RMVar_hsa_circ_193352,RMVar_hsa_circ_193353 55299 RMVar_ID_55299 Human_SNP_ID_660223463 m1A Human chr19 - 17581552 17581552 17581552 TAGCAAGAGCTGGCTGGACACCACCCCACACGAGAGCCCTCTGTGGCCTGCCAAGGGGTCCAGAG TAGCAAGAGCTGGCTGGACACCACCCCACACGGGAGCCCTCTGTGGCCTGCCAAGGGGTCCAGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17581226..17581600 32194978 MeRIP-seq:(Medium) rs965846834 Functional Loss SNV dbSNP153 33..33 33 - - - 55300 RMVar_ID_55300 Human_SNP_ID_660262390 m1A Human chr19 + 17720400 17720400 17720400 CTTTGGGCAGTGGACACAGGGATATGGCCGGGATGATAGACAGGTTCAGCCCTGCCAACACAGGT CTTTGGGCAGTGGACACAGGGATATGGCCGGGGTGATAGACAGGTTCAGCCCTGCCAACACAGGT A G MAP1S Ensembl:ENSG00000130479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17720397..17720789 26863196 MeRIP-seq:(Medium) rs1568289052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1977955 55301 RMVar_ID_55301 Human_SNP_ID_660264643 m1A Human chr19 + 17726838 17726838 17726838 GAGCGTGGGCTCCCGGGACAGCTCGAAGAGAGAGGGCCTCCTGGCCACCCACCCTAGACCTGGCC GAGCGTGGGCTCCCGGGACAGCTCGAAGAGAGCGGGCCTCCTGGCCACCCACCCTAGACCTGGCC A C MAP1S Ensembl:ENSG00000130479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17726792..17727153 26863196 MeRIP-seq:(Medium) rs770623549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10143,RMVar_hsa_circ_46934,RMVar_hsa_circ_193373,RMVar_hsa_circ_106091 55302 RMVar_ID_55302 Human_SNP_ID_660264644 m1A Human chr19 + 17726838 17726838 17726838 GAGCGTGGGCTCCCGGGACAGCTCGAAGAGAGAGGGCCTCCTGGCCACCCACCCTAGACCTGGCC GAGCGTGGGCTCCCGGGACAGCTCGAAGAGAGGGGGCCTCCTGGCCACCCACCCTAGACCTGGCC A G MAP1S Ensembl:ENSG00000130479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17726792..17727153 26863196 MeRIP-seq:(Medium) rs770623549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10143,RMVar_hsa_circ_46934,RMVar_hsa_circ_193373,RMVar_hsa_circ_106091 55303 RMVar_ID_55303 Human_SNP_ID_660264772 m1A Human chr19 - 17727027 17727027 17727027 CCGCCTGGGCATTCGTCTTCTTGAGGTTGGGCACAGAAGAGGCTGCCCGGCGCACCTCCCGCGGC CCGCCTGGGCATTCGTCTTCTTGAGGTTGGGCCCAGAAGAGGCTGCCCGGCGCACCTCCCGCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17726977..17727184 26863196 MeRIP-seq:(Medium) rs775022856 Functional Loss SNV dbSNP153 33..33 33 - - - 55304 RMVar_ID_55304 Human_SNP_ID_660264943 m1A Human chr19 - 17727216 17727216 17727216 TCTCCTCCCCGGCTGGGATCGGCCCCAGCTCCAGGCTGGGCGTGGCCACCAGCTGGGAGGCCGGA TCTCCTCCCCGGCTGGGATCGGCCCCAGCTCCGGGCTGGGCGTGGCCACCAGCTGGGAGGCCGGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:17727122..17727223 26863410 MeRIP-seq:(Medium) rs1274316164 Functional Loss SNV dbSNP153 33..33 33 - - - 55305 RMVar_ID_55305 Human_SNP_ID_660265211 m1A Human chr19 - 17727575 17727575 17727575 TGACACCAGGCACAGGTCCACATCGTGTGGGGAAGCCGAGCGCCGCGCCCGGGGGCCACGCAGCG TGACACCAGGCACAGGTCCACATCGTGTGGGGGAGCCGAGCGCCGCGCCCGGGGGCCACGCAGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17727526..17728120 26863196 MeRIP-seq:(Medium) rs930299075 Functional Loss SNV dbSNP153 33..33 33 - - - 55306 RMVar_ID_55306 Human_SNP_ID_660265376 m1A Human chr19 - 17727853 17727853 17727853 AGTGGTGGGGGGACCTTGAGGGGGTCAGGCAAAGGGTCGTGGCGAGGGACTCCAAAGCCCTCTGT AGTGGTGGGGGGACCTTGAGGGGGTCAGGCAAGGGGTCGTGGCGAGGGACTCCAAAGCCCTCTGT T C AC008761.1 Ensembl:ENSG00000268112 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17727725..17727967 26863196 MeRIP-seq:(Medium) rs1051210860 Functional Loss SNV dbSNP153 33..33 33 - - - 55307 RMVar_ID_55307 Human_SNP_ID_660280834 m1A Human chr19 + 17783124 17783124 17783124 ACCACCACCTGTCCTCAGCTTCCGGCTTGTACACACAACCGCTATTGAGCACTTCCAGCCCAACG ACCACCACCTGTCCTCAGCTTCCGGCTTGTACTCACAACCGCTATTGAGCACTTCCAGCCCAACG A T FCHO1 Ensembl:ENSG00000130475 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17783074..17784206 26863196 MeRIP-seq:(Medium) rs1490294238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1978065,Human_Splice_Rec_1978111,Human_Splice_Rec_1978161,Human_Splice_Rec_1978323,Human_Splice_Rec_1978459,Human_Splice_Rec_1978543,Human_Splice_Rec_1978601,Human_Splice_Rec_1978661 RMVar_hsa_circ_193388,RMVar_hsa_circ_340626,RMVar_hsa_circ_331038 55308 RMVar_ID_55308 Human_SNP_ID_660302613 m1A Human chr19 + 17859941 17859941 17859941 CAGAGGACACTTCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCACGCCATGAAGGCCTCGGGCAC CAGAGGACACTTCCTTTTGCGGGTGGCGGCGAGCGCGGAGAGCACGCCATGAAGGCCTCGGGCAC A G RPL18A Ensembl:ENSG00000105640 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17859895..17860190 26863196 MeRIP-seq:(Medium) rs552181732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55309 RMVar_ID_55309 Human_SNP_ID_660302624 m1A Human chr19 + 17859949 17859949 17859949 ACTTCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCACGCCATGAAGGCCTCGGGCACGGTAAGGC ACTTCCTTTTGCGGGTGGCGGCGAACGCGGAGGGCACGCCATGAAGGCCTCGGGCACGGTAAGGC A G RPL18A Ensembl:ENSG00000105640 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs113971469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558225,Human_RBP_ID_5373484 Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 Human_miRNA_ID_1966615,Human_miRNA_ID_2196198,Human_miRNA_ID_2362073 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55310 RMVar_ID_55310 Human_SNP_ID_660302628 m1A Human chr19 + 17859952 17859952 17859952 TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCACGCCATGAAGGCCTCGGGCACGGTAAGGCGGG TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCCCGCCATGAAGGCCTCGGGCACGGTAAGGCGGG A C RPL18A Ensembl:ENSG00000105640 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17859901..17860225 26863196 MeRIP-seq:(Medium) rs201563703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558225,Human_RBP_ID_5373484,Human_RBP_ID_19092735 Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 Human_miRNA_ID_1966615,Human_miRNA_ID_2196198,Human_miRNA_ID_2362073 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55311 RMVar_ID_55311 Human_SNP_ID_660302629 m1A Human chr19 + 17859952 17859952 17859952 TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCACGCCATGAAGGCCTCGGGCACGGTAAGGCGGG TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCGCGCCATGAAGGCCTCGGGCACGGTAAGGCGGG A G RPL18A Ensembl:ENSG00000105640 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17859901..17860225 26863196 MeRIP-seq:(Medium) rs201563703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558225,Human_RBP_ID_5373484,Human_RBP_ID_19092735 Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 Human_miRNA_ID_1966615,Human_miRNA_ID_2196198,Human_miRNA_ID_2362073 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55312 RMVar_ID_55312 Human_SNP_ID_660302630 m1A Human chr19 + 17859952 17859952 17859952 TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCACGCCATGAAGGCCTCGGGCACGGTAAGGCGGG TCCTTTTGCGGGTGGCGGCGAACGCGGAGAGCTCGCCATGAAGGCCTCGGGCACGGTAAGGCGGG A T RPL18A Ensembl:ENSG00000105640 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17859901..17860225 26863196 MeRIP-seq:(Medium) rs201563703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558225,Human_RBP_ID_5373484,Human_RBP_ID_19092735 Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 Human_miRNA_ID_1966615,Human_miRNA_ID_2196198,Human_miRNA_ID_2362073 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55313 RMVar_ID_55313 Human_SNP_ID_660302648 m1A Human chr19 + 17859972 17859972 17859972 AACGCGGAGAGCACGCCATGAAGGCCTCGGGCACGGTAAGGCGGGCGCGGCGCGGCAGGGGGCCA AACGCGGAGAGCACGCCATGAAGGCCTCGGGCCCGGTAAGGCGGGCGCGGCGCGGCAGGGGGCCA A C RPL18A Ensembl:ENSG00000105640 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control chr19:17859901..17860046;chr19:17859901..17860050;chr19:17859926..17860000;chr19:17859926..17860030;chr19:17859926..17860039 26863410 MeRIP-seq:(Medium) rs1383035964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239829,Human_RBP_ID_4558226,Human_RBP_ID_5373484,Human_RBP_ID_19089674 Human_Splice_Rec_1978879,Human_Splice_Rec_1978887,Human_Splice_Rec_1978893,Human_Splice_Rec_1978903 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55314 RMVar_ID_55314 Human_SNP_ID_660303090 m1A Human chr19 - 17861218 17861218 17861218 CAACTGTGGAGATCCACCTCACTCCCTTTCCTACATCTAGTGACCACAGATTCGGGAAGCAGGAG CAACTGTGGAGATCCACCTCACTCCCTTTCCTGCATCTAGTGACCACAGATTCGGGAAGCAGGAG T C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17861168..17861418 32194978 MeRIP-seq:(Medium) rs11880203 Functional Loss SNV dbSNP153 33..33 33 - - - 55315 RMVar_ID_55315 Human_SNP_ID_660303091 m1A Human chr19 - 17861218 17861218 17861218 CAACTGTGGAGATCCACCTCACTCCCTTTCCTACATCTAGTGACCACAGATTCGGGAAGCAGGAG CAACTGTGGAGATCCACCTCACTCCCTTTCCTCCATCTAGTGACCACAGATTCGGGAAGCAGGAG T G L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17861168..17861418 32194978 MeRIP-seq:(Medium) rs11880203 Functional Loss SNV dbSNP153 33..33 33 - - - 55316 RMVar_ID_55316 Human_SNP_ID_660303097 m1A Human chr19 + 17861244 17861244 17861244 TAGATGTAGGAAAGGGAGTGAGGTGGATCTCCACAGTTGCCTCTGGGTGCTGGCCTTACCCTCAC TAGATGTAGGAAAGGGAGTGAGGTGGATCTCCGCAGTTGCCTCTGGGTGCTGGCCTTACCCTCAC A G RPL18A Ensembl:ENSG00000105640 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:17861242..17861400 26863410 MeRIP-seq:(Medium) rs200698036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910955,Human_RBP_ID_1292451,Human_RBP_ID_5373487,Human_RBP_ID_22545793 Human_Splice_Rec_1978895 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395 55317 RMVar_ID_55317 Human_SNP_ID_660303197 m1A Human chr19 + 17861479 17861479 17861479 CAGGGGAGATTGTCTACTGTGGGCAGGTATGGAGAGGCCGGGGCTACGTGGGGTCTGGAGTGGAT CAGGGGAGATTGTCTACTGTGGGCAGGTATGGTGAGGCCGGGGCTACGTGGGGTCTGGAGTGGAT A T RPL18A Ensembl:ENSG00000105640 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17861476..17861735 26863196 MeRIP-seq:(Medium) rs767107214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825084,Human_RBP_ID_2559011,Human_RBP_ID_18490437,Human_RBP_ID_19089676,Human_RBP_ID_22069988,Human_RBP_ID_26785454,Human_RBP_ID_27839323 Human_Splice_Rec_1978896 RMVar_hsa_circ_83119,RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_123110,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_193395,RMVar_hsa_circ_98959,RMVar_hsa_circ_193398,RMVar_hsa_circ_193399 55318 RMVar_ID_55318 Human_SNP_ID_660303251 m1A Human chr19 - 17861565 17861565 17861565 ATGTGATGGGATTACAGGCGTTGAGCTACCGCACCCGTTCGATGTCTGATTAATTCTTGAGATGC ATGTGATGGGATTACAGGCGTTGAGCTACCGCGCCCGTTCGATGTCTGATTAATTCTTGAGATGC T C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:17861463..17861810 26863196 MeRIP-seq:(Medium) rs1246617250 Functional Loss SNV dbSNP153 33..33 33 - - - 55319 RMVar_ID_55319 Human_SNP_ID_660323671 m1A Human chr19 + 17933047 17933047 17933047 GGAGGCGCGACCGGGCCGGCGCTGGGGTAAGAAGGTAGGAGCGTCTGCGGCGCGGGCGGAACCCG GGAGGCGCGACCGGGCCGGCGCTGGGGTAAGAGGGTAGGAGCGTCTGCGGCGCGGGCGGAACCCG A G CCDC124 Ensembl:ENSG00000007080 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:17933001..17933141;chr19:17933001..17933327 26863196 MeRIP-seq:(Medium) rs931745355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1978955,Human_Splice_Rec_1978963 55320 RMVar_ID_55320 Human_SNP_ID_660324742 m1A Human chr19 + 17936578 17936577 17936579 CGACAAACACGTCATGAGGAAGGAGCAGCGCAAGGTGCGTGCACTCCGAGTCCCCGCGGCCCGCA CGACAAACACGTCATGAGGAAGGAGCAGCGCA__GTGCGTGCACTCCGAGTCCCCGCGGCCCGCA AAG A CCDC124 Ensembl:ENSG00000007080 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17936551..17936600 26863196 MeRIP-seq:(Medium) rs769909710 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26336026 Human_Splice_Rec_1978957,Human_Splice_Rec_1978967,Human_Splice_Rec_1978973 RMVar_hsa_circ_55946,RMVar_hsa_circ_101232,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406,RMVar_hsa_circ_311205 55321 RMVar_ID_55321 Human_SNP_ID_660326381 m1A Human chr19 + 17942662 17942659 17942662 CCTGACCATGCACGCCGCCCCCGCAGGAGGAGAAGGAGAAGCGGCGCCTCGACCAGCTGGAACGT CCTGACCATGCACGCCGCCCCCGCAGGAGG___AGGAGAAGCGGCGCCTCGACCAGCTGGAACGT GAGA G CCDC124 Ensembl:ENSG00000007080 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17942651..17942700 26863196 MeRIP-seq:(Medium) rs774788725 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_52467,Human_RBP_ID_515941,Human_RBP_ID_4509663,Human_RBP_ID_26336027 Human_Splice_Rec_1978958,Human_Splice_Rec_1978968,Human_Splice_Rec_1978974 RMVar_hsa_circ_55946,RMVar_hsa_circ_101232,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408 55322 RMVar_ID_55322 Human_SNP_ID_660326383 m1A Human chr19 + 17942662 17942662 17942662 CCTGACCATGCACGCCGCCCCCGCAGGAGGAGAAGGAGAAGCGGCGCCTCGACCAGCTGGAACGT CCTGACCATGCACGCCGCCCCCGCAGGAGGAGGAGGAGAAGCGGCGCCTCGACCAGCTGGAACGT A G CCDC124 Ensembl:ENSG00000007080 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17942651..17942700 26863196 MeRIP-seq:(Medium) rs752183430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52467,Human_RBP_ID_515941,Human_RBP_ID_4509663,Human_RBP_ID_26336027 Human_Splice_Rec_1978958,Human_Splice_Rec_1978968,Human_Splice_Rec_1978974 RMVar_hsa_circ_55946,RMVar_hsa_circ_101232,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408 55323 RMVar_ID_55323 Human_SNP_ID_660326666 m1A Human chr19 - 17943318 17943314 17943318 TGGTGCGCGCCTCCACGCTGCCCTCCTCCAGCACGCGGCGGTTCACGTTCTCCTCCAGCGGCACC TGGTGCGCGCCTCCACGCTGCCCTCCTCCAGC____GGCGGTTCACGTTCTCCTCCAGCGGCACC CGCGT C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17943251..17943350 26863196 MeRIP-seq:(Medium) rs781381727 Functional Loss DEL dbSNP153 33..36 33 - - - 55324 RMVar_ID_55324 Human_SNP_ID_660326673 m1A Human chr19 - 17943321 17943321 17943321 CGATGGTGCGCGCCTCCACGCTGCCCTCCTCCAGCACGCGGCGGTTCACGTTCTCCTCCAGCGGC CGATGGTGCGCGCCTCCACGCTGCCCTCCTCCGGCACGCGGCGGTTCACGTTCTCCTCCAGCGGC T C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17943251..17943400 26863196 MeRIP-seq:(Medium) rs199982966 Functional Loss SNV dbSNP153 33..33 33 - - - 55325 RMVar_ID_55325 Human_SNP_ID_660326879 m1A Human chr19 - 17943678 17943678 17943678 TGGGGGCATTGAAGGGCACGGCCCGCTGGTTCATGGGGTTGTCAGGAGAGCGGAGCCACTCCTTC TGGGGGCATTGAAGGGCACGGCCCGCTGGTTCTTGGGGTTGTCAGGAGAGCGGAGCCACTCCTTC T A L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17943499..17944000 26863196 MeRIP-seq:(Medium) rs1195402019 Functional Loss SNV dbSNP153 33..33 33 - - - 55326 RMVar_ID_55326 Human_SNP_ID_660341876 m1A Human chr19 + 17998323 17998323 17998323 CCATACGCCCACCCCCGCCTCCCCTGCCTCCCAGGCCCGGCCCCGGCCCCCAAGACCAGGCAGCC CCATACGCCCACCCCCGCCTCCCCTGCCTCCCCGGCCCGGCCCCGGCCCCCAAGACCAGGCAGCC A C KCNN1 Ensembl:ENSG00000105642 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17998312..17998401 26863196 MeRIP-seq:(Medium) rs1388942202 Functional Loss SNV dbSNP153 33..33 33 - - - 55327 RMVar_ID_55327 Human_SNP_ID_660342831 m1A Human chr19 + 18001183 18001183 18001183 CGCGCCCGCCCTGGGCCACCGGCGCCGGCCCAAGTTCGCCGGGGGGGCCCGGAGGAAGCTTGGGG CGCGCCCGCCCTGGGCCACCGGCGCCGGCCCAGGTTCGCCGGGGGGGCCCGGAGGAAGCTTGGGG A G ARRDC2 Ensembl:ENSG00000105643 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:18001144..18001268;chr19:18001134..18001257 26863196 MeRIP-seq:(Medium) rs974489890 Functional Loss SNV dbSNP153 33..33 33 - - - 55328 RMVar_ID_55328 Human_SNP_ID_660342832 m1A Human chr19 - 18001186 18001186 18001186 GTCCCCCAAGCTTCCTCCGGGCCCCCCCGGCGAACTTGGGCCGGCGCCGGTGGCCCAGGGCGGGC GTCCCCCAAGCTTCCTCCGGGCCCCCCCGGCGGACTTGGGCCGGCGCCGGTGGCCCAGGGCGGGC T C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18001135..18001601 26863196 MeRIP-seq:(Medium) rs1388589504 Functional Loss SNV dbSNP153 33..33 33 - - - 55329 RMVar_ID_55329 Human_SNP_ID_660344710 m1A Human chr19 - 18006575 18006575 18006575 ACGGTCTCCCTCTCATGCCGAGCAGAAGCTGGACTGTGCTGCTGCCATCTCGGCTCACTGCAACC ACGGTCTCCCTCTCATGCCGAGCAGAAGCTGGGCTGTGCTGCTGCCATCTCGGCTCACTGCAACC T C L13712-001,RF00017-124 RNACentral:URS0000334622,RNACentral:URS000099C5B7 misc_RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18006561..18006690 26863196 MeRIP-seq:(Medium) rs972012549 Functional Loss SNV dbSNP153 33..33 33 - - - 55330 RMVar_ID_55330 Human_SNP_ID_660349747 m1A Human chr19 + 18022451 18022451 18022451 CCATCTTGGACGCATGATGATGGCAGTGGATCAGAGTCCCAAGGACACTGGTGAAGATCAGAGCA CCATCTTGGACGCATGATGATGGCAGTGGATCTGAGTCCCAAGGACACTGGTGAAGATCAGAGCA A T AC020904.2 Ensembl:ENSG00000273654 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18022401..18022661 26863196 MeRIP-seq:(Medium) rs532996037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13393126,Human_RBP_ID_18724400 55331 RMVar_ID_55331 Human_SNP_ID_660375886 m1A Human chr19 + 18120065 18120065 18120065 AACTTCCTTCTGTCAAGGTGTGGGCTGAGGCCAGGGCCCAGGTGGGAGAAGAAGCCAGGCAGGGT AACTTCCTTCTGTCAAGGTGTGGGCTGAGGCCCGGGCCCAGGTGGGAGAAGAAGCCAGGCAGGGT A C MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18120060..18120159 26863196 MeRIP-seq:(Medium) rs1029635107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78001,RMVar_hsa_circ_193417 55332 RMVar_ID_55332 Human_SNP_ID_660378353 m1A Human chr19 + 18128506 18128506 18128506 TGGGGGACCCCCGCTCATCTTGTTCTTTCCAGAGTGGACCAGGCACCCGCAGAAAGGGCTGGGTT TGGGGGACCCCCGCTCATCTTGTTCTTTCCAGGGTGGACCAGGCACCCGCAGAAAGGGCTGGGTT A G MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18128503..18128637 32194978 MeRIP-seq:(Medium) rs1447388291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52857,Human_RBP_ID_910961,Human_RBP_ID_2559075,Human_RBP_ID_5373495,Human_RBP_ID_19089683,Human_RBP_ID_23257492 RMVar_hsa_circ_44924,RMVar_hsa_circ_193419,RMVar_hsa_circ_120277,RMVar_hsa_circ_98729,RMVar_hsa_circ_118963,RMVar_hsa_circ_193418,RMVar_hsa_circ_71247,RMVar_hsa_circ_121314,RMVar_hsa_circ_193423,RMVar_hsa_circ_112186,RMVar_hsa_circ_193427,RMVar_hsa_circ_193429,RMVar_hsa_circ_78180,RMVar_hsa_circ_193428,RMVar_hsa_circ_52932,RMVar_hsa_circ_111759,RMVar_hsa_circ_193430 55333 RMVar_ID_55333 Human_SNP_ID_660383852 m1A Human chr19 + 18147599 18147599 18147599 AGCCTCTCCCCCAGCCCCACCACTCCCTGCCGAAGCCCAGCCCCTGATGTCCCAGCAGGTGGGTG AGCCTCTCCCCCAGCCCCACCACTCCCTGCCGTAGCCCAGCCCCTGATGTCCCAGCAGGTGGGTG A T MAST3 Ensembl:ENSG00000099308 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18147508..18147662 26863196 MeRIP-seq:(Medium) rs765040327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979239 RMVar_hsa_circ_112186,RMVar_hsa_circ_193429,RMVar_hsa_circ_29104,RMVar_hsa_circ_48676,RMVar_hsa_circ_287129 55334 RMVar_ID_55334 Human_SNP_ID_660384271 m1A Human chr19 + 18149183 18149183 18149183 ATTGAGGCCAGCAGCCCTGACCTACGCTTATCACCCACAGATACCACTGCATCCCCACCCAGCGC ATTGAGGCCAGCAGCCCTGACCTACGCTTATCGCCCACAGATACCACTGCATCCCCACCCAGCGC A G MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18149182..18149429 26863196 MeRIP-seq:(Medium) rs376887561 Functional Loss SNV dbSNP153 33..33 33 - - - 55335 RMVar_ID_55335 Human_SNP_ID_660384283 m1A Human chr19 + 18149207 18149207 18149207 CGCTTATCACCCACAGATACCACTGCATCCCCACCCAGCGCATCCCCGAGCTCCAGCAGCCCCGC CGCTTATCACCCACAGATACCACTGCATCCCCCCCCAGCGCATCCCCGAGCTCCAGCAGCCCCGC A C MAST3 Ensembl:ENSG00000099308 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18149203..18149309 26863196 MeRIP-seq:(Medium) rs997562077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979240 55336 RMVar_ID_55336 Human_SNP_ID_660384284 m1A Human chr19 + 18149207 18149207 18149207 CGCTTATCACCCACAGATACCACTGCATCCCCACCCAGCGCATCCCCGAGCTCCAGCAGCCCCGC CGCTTATCACCCACAGATACCACTGCATCCCCTCCCAGCGCATCCCCGAGCTCCAGCAGCCCCGC A T MAST3 Ensembl:ENSG00000099308 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18149203..18149309 26863196 MeRIP-seq:(Medium) rs997562077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979240 55337 RMVar_ID_55337 Human_SNP_ID_660386458 m1A Human chr19 - 18156143 18156143 18156143 CTGGCGGGCAGTGGGCGGGGGCCCCGTGGGCGAGGGCCGGGCCGGGCCAGGGCCACGGGCCCCAG CTGGCGGGCAGTGGGCGGGGGCCCCGTGGGCGTGGGCCGGGCCGGGCCAGGGCCACGGGCCCCAG T A RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18155968..18156225 26863410 MeRIP-seq:(Medium) rs753655968 Functional Loss SNV dbSNP153 33..33 33 - - - 55338 RMVar_ID_55338 Human_SNP_ID_660386459 m1A Human chr19 - 18156143 18156143 18156143 CTGGCGGGCAGTGGGCGGGGGCCCCGTGGGCGAGGGCCGGGCCGGGCCAGGGCCACGGGCCCCAG CTGGCGGGCAGTGGGCGGGGGCCCCGTGGGCGGGGGCCGGGCCGGGCCAGGGCCACGGGCCCCAG T C RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18155968..18156225 26863410 MeRIP-seq:(Medium) rs753655968 Functional Loss SNV dbSNP153 33..33 33 - - - 55339 RMVar_ID_55339 Human_SNP_ID_660387767 m1A Human chr19 + 18160931 18160931 18160931 CCTGTCCCCTTCACCCCCAGGGCTGGACAGCGAATCTCACTACCGCCCGGAGCTGCCCGCACCGC CCTGTCCCCTTCACCCCCAGGGCTGGACAGCGCATCTCACTACCGCCCGGAGCTGCCCGCACCGC A C PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18160926..18160975 26863196 MeRIP-seq:(Medium) rs1333104337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910969,Human_RBP_ID_19089692,Human_RBP_ID_22545801,Human_RBP_ID_23257745 Human_Splice_Rec_1979286,Human_Splice_Rec_1979287,Human_Splice_Rec_1979334,Human_Splice_Rec_1979335,Human_Splice_Rec_1979362,Human_Splice_Rec_1979363,Human_Splice_Rec_1979390,Human_Splice_Rec_1979391,Human_Splice_Rec_1979410,Human_Splice_Rec_1979411,Human_Splice_Rec_1979435 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_60955,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_193438 55340 RMVar_ID_55340 Human_SNP_ID_660390171 m1A Human chr19 + 18168527 18168527 18168527 CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGATTAAAAATGAGACTGAGGAGTGAGTGACCGTC CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGGTTAAAAATGAGACTGAGGAGTGAGTGACCGTC A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18168439..18168582 26863196 MeRIP-seq:(Medium) rs767446008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979306,Human_Splice_Rec_1979307,Human_Splice_Rec_1979354,Human_Splice_Rec_1979355,Human_Splice_Rec_1979382,Human_Splice_Rec_1979383,Human_Splice_Rec_1979430,Human_Splice_Rec_1979431,Human_Splice_Rec_1979450,Human_Splice_Rec_1979451,Human_Splice_Rec_1979456,Human_Splice_Rec_1979457 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445 55341 RMVar_ID_55341 Human_SNP_ID_660390271 m1A Human chr19 + 18168774 18168774 18168774 GAGGACGAGGACGATCTCCCGCACCACGAGGAACGCACTTGGTACGTGGGCAAGATCAACCGCAC GAGGACGAGGACGATCTCCCGCACCACGAGGACCGCACTTGGTACGTGGGCAAGATCAACCGCAC A C PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18168690..18168874 26863196 MeRIP-seq:(Medium) rs1396135468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380802,Human_RBP_ID_22978067 Human_Splice_Rec_1979308,Human_Splice_Rec_1979356,Human_Splice_Rec_1979384,Human_Splice_Rec_1979432,Human_Splice_Rec_1979452,Human_Splice_Rec_1979458 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445 55342 RMVar_ID_55342 Human_SNP_ID_660390537 m1A Human chr19 - 18169282 18169282 18169282 TTGGGGCGGGTCCTCGGTGCTCAGCGGGCGGCAGGCGGCGGGCCGGGGCCCGGGGCGCGCACTGG TTGGGGCGGGTCCTCGGTGCTCAGCGGGCGGCCGGCGGCGGGCCGGGGCCCGGGGCGCGCACTGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18169176..18169525 26863196 MeRIP-seq:(Medium) rs1411008837 Functional Loss SNV dbSNP153 33..33 33 - - - 55343 RMVar_ID_55343 Human_SNP_ID_660390549 m1A Human chr19 + 18169304 18169304 18169304 GCCCGCCGCCTGCCGCCCGCTGAGCACCGAGGACCCGCCCCAAGCAGAGCCGCCCCTGGGCCCGT GCCCGCCGCCTGCCGCCCGCTGAGCACCGAGGGCCCGCCCCAAGCAGAGCCGCCCCTGGGCCCGT A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18169255..18169576 26863196 MeRIP-seq:(Medium) rs1025450781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2387394,Human_miRNA_ID_2388867,Human_miRNA_ID_2396224,Human_miRNA_ID_2400014,Human_miRNA_ID_3031075,Human_miRNA_ID_3070133 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_84904,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_193447 55344 RMVar_ID_55344 Human_SNP_ID_660390555 m1A Human chr19 + 18169317 18169317 18169317 CGCCCGCTGAGCACCGAGGACCCGCCCCAAGCAGAGCCGCCCCTGGGCCCGTCTGCGCCGGAGGC CGCCCGCTGAGCACCGAGGACCCGCCCCAAGCGGAGCCGCCCCTGGGCCCGTCTGCGCCGGAGGC A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18169275..18169434 26863196 MeRIP-seq:(Medium) rs1288112746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824880,Human_RBP_ID_17917072 Human_miRNA_ID_2387395,Human_miRNA_ID_2388868,Human_miRNA_ID_2396224,Human_miRNA_ID_2400015,Human_miRNA_ID_3031076,Human_miRNA_ID_3070133 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_84904,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_193447 55345 RMVar_ID_55345 Human_SNP_ID_660390729 m1A Human chr19 + 18169786 18169786 18169786 TCACTCTGCTGCTTCCGAGAACCTCGGCCGTGACATTCGGGGCCGGGCGGGACCCGCCCCACAGA TCACTCTGCTGCTTCCGAGAACCTCGGCCGTGGCATTCGGGGCCGGGCGGGACCCGCCCCACAGA A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18169736..18169896 26863196 MeRIP-seq:(Medium) rs1031893166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516031,Human_RBP_ID_770963,Human_RBP_ID_27465265 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_84904,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_193447 55346 RMVar_ID_55346 Human_SNP_ID_660390896 m1A Human chr19 + 18170247 18170247 18170247 AAATAAATAAATAAACTTGTGAGCTGGCCCCAACCCCTCCTAGGAATCACAGCTCCCCGTACTGG AAATAAATAAATAAACTTGTGAGCTGGCCCCAGCCCCTCCTAGGAATCACAGCTCCCCGTACTGG A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18170197..18170313 26863196 MeRIP-seq:(Medium) rs762326151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516035,Human_RBP_ID_8197627,Human_RBP_ID_27465266 Human_miRNA_ID_465543,Human_miRNA_ID_465544,Human_miRNA_ID_1560749,Human_miRNA_ID_1560750,Human_miRNA_ID_2153885,Human_miRNA_ID_2569675,Human_miRNA_ID_2801761,Human_miRNA_ID_3009893 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_84904,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_193447 55347 RMVar_ID_55347 Human_SNP_ID_660392144 m1A Human chr19 - 18175030 18175030 18175030 CCCCGCAGGTATAGATTGCCTGTCTGTGGATTAGGAAGGCGTGGGAGGCAGGTGTAGCCCTGGGC CCCCGCAGGTATAGATTGCCTGTCTGTGGATTGGGAAGGCGTGGGAGGCAGGTGTAGCCCTGGGC T C lnc-RAB3A-5 RNACentral:URS0000D5AA85 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18175026..18175050 26863196 MeRIP-seq:(Medium) rs766690181 Functional Loss SNV dbSNP153 33..33 33 - - - 55348 RMVar_ID_55348 Human_SNP_ID_660392145 m1A Human chr19 - 18175030 18175030 18175030 CCCCGCAGGTATAGATTGCCTGTCTGTGGATTAGGAAGGCGTGGGAGGCAGGTGTAGCCCTGGGC CCCCGCAGGTATAGATTGCCTGTCTGTGGATTCGGAAGGCGTGGGAGGCAGGTGTAGCCCTGGGC T G lnc-RAB3A-5 RNACentral:URS0000D5AA85 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18175026..18175050 26863196 MeRIP-seq:(Medium) rs766690181 Functional Loss SNV dbSNP153 33..33 33 - - - 55349 RMVar_ID_55349 Human_SNP_ID_660392881 m1A Human chr19 + 18177228 18177228 18177228 GGGGGACCGCGGCATGCAGCTCATGCACGCCAACGCCCAGCGGACAGATGCTCTCCAGCCACCAC GGGGGACCGCGGCATGCAGCTCATGCACGCCACCGCCCAGCGGACAGATGCTCTCCAGCCACCAC A C IFI30,AC007192.1 Ensembl:ENSG00000216490,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18177106..18177227 26863196 MeRIP-seq:(Medium) rs759814847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54735,Human_RBP_ID_17656885,Human_RBP_ID_22448520,Human_RBP_ID_22762881,Human_RBP_ID_23786455 Human_Splice_Rec_1979324,Human_Splice_Rec_1979325,Human_Splice_Rec_1979474,Human_Splice_Rec_1979475,Human_Splice_Rec_1979484 RMVar_hsa_circ_78293,RMVar_hsa_circ_78260,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_79824,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_88153,RMVar_hsa_circ_104394,RMVar_hsa_circ_114247,RMVar_hsa_circ_193448,RMVar_hsa_circ_193450,RMVar_hsa_circ_85983,RMVar_hsa_circ_193449,RMVar_hsa_circ_116562,RMVar_hsa_circ_193451,RMVar_hsa_circ_96104,RMVar_hsa_circ_193453,RMVar_hsa_circ_193454,RMVar_hsa_circ_193452 55350 RMVar_ID_55350 Human_SNP_ID_660393168 m1A Human chr19 - 18178002 18178002 18178002 TTCATGGGATGCATAAAATTTTCCAGTTGGTAAGTAGCAGGTGCCGAGGGTCTGGATCAGAAAAA TTCATGGGATGCATAAAATTTTCCAGTTGGTAGGTAGCAGGTGCCGAGGGTCTGGATCAGAAAAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18177951..18178025 26863196 MeRIP-seq:(Medium) rs988546380 Functional Loss SNV dbSNP153 33..33 33 - - - 55351 RMVar_ID_55351 Human_SNP_ID_660393178 m1A Human chr19 + 18178030 18178030 18178030 CTACTTACCAACTGGAAAATTTTATGCATCCCATGAAGCCCAGATACACAAAATTCCACCCCATG CTACTTACCAACTGGAAAATTTTATGCATCCCGTGAAGCCCAGATACACAAAATTCCACCCCATG A G IFI30,AC007192.1 Ensembl:ENSG00000216490,Ensembl:ENSG00000268173 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18177860..18178054 26863196 MeRIP-seq:(Medium) rs575384663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54736,Human_RBP_ID_516048,Human_RBP_ID_5116174,Human_RBP_ID_17272640,Human_RBP_ID_17656890,Human_RBP_ID_17935287 Human_miRNA_ID_2555179,Human_miRNA_ID_2555180 RMVar_hsa_circ_78293,RMVar_hsa_circ_78260,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_193438,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_88153,RMVar_hsa_circ_104394,RMVar_hsa_circ_114247,RMVar_hsa_circ_193448,RMVar_hsa_circ_193450,RMVar_hsa_circ_116562,RMVar_hsa_circ_193451,RMVar_hsa_circ_193452,RMVar_hsa_circ_115315,RMVar_hsa_circ_193458 55352 RMVar_ID_55352 Human_SNP_ID_660398806 m1A Human chr19 + 18197225 18197225 18197225 GGGTGAGCGGTGAGTTCACGGGGCCACGAGACACCACAGCTGAGTGGGGAAAGGGCTATATGTAC GGGTGAGCGGTGAGTTCACGGGGCCACGAGACGCCACAGCTGAGTGGGGAAAGGGCTATATGTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18197176..18197485 26863196 MeRIP-seq:(Medium) rs1184774532 Functional Loss SNV dbSNP153 33..33 33 - - - 55353 RMVar_ID_55353 Human_SNP_ID_660422732 m1A Human chr19 - 18280069 18280064 18280069 GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTACTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA GCAGCCTCAAACCCTGCCTTTCCTTTACTTTT_____TTTTTTTTTTTCTTTGGAAGAGAGAAGA AAAAGT A JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18280001..18280875 32194978 MeRIP-seq:(Medium) rs1236066914 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3564534,Human_RBP_ID_6726568,Human_RBP_ID_23786500,Human_RBP_ID_24418535 55354 RMVar_ID_55354 Human_SNP_ID_660422733 m1A Human chr19 - 18280069 18280065 18280069 GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTACTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA GCAGCCTCAAACCCTGCCTTTCCTTTACTTTT____TTTTTTTTTTTTCTTTGGAAGAGAGAAGA AAAGT A JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18280001..18280875 32194978 MeRIP-seq:(Medium) rs1382415155 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3564534,Human_RBP_ID_6726568,Human_RBP_ID_23786500,Human_RBP_ID_24418535 55355 RMVar_ID_55355 Human_SNP_ID_660422738 m1A Human chr19 - 18280069 18280069 18280069 GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTACTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTTCTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA T A JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18280001..18280875 32194978 MeRIP-seq:(Medium) rs1034061105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3564534,Human_RBP_ID_6726568,Human_RBP_ID_23786500,Human_RBP_ID_24418535 55356 RMVar_ID_55356 Human_SNP_ID_660422739 m1A Human chr19 - 18280069 18280069 18280069 GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTACTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA GCAGCCTCAAACCCTGCCTTTCCTTTACTTTTCCTTTTTTTTTTTTTTCTTTGGAAGAGAGAAGA T G JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18280001..18280875 32194978 MeRIP-seq:(Medium) rs1034061105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3564534,Human_RBP_ID_6726568,Human_RBP_ID_23786500,Human_RBP_ID_24418535 55357 RMVar_ID_55357 Human_SNP_ID_660422755 m1A Human chr19 - 18280119 18280109 18280120 CTCGGCTGCCCCTTTGTACACCGCGCCGCGGAAGGGGGCTCCGAGGGGGCGCAGCCTCAAACCCT CTCGGCTGCCCCTTTGTACACCGCGCCGCGG___________GAGGGGGCGCAGCCTCAAACCCT CGGAGCCCCCTT C JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18280076..18280900 26863196 MeRIP-seq:(Medium) rs1439394179 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_516092,Human_RBP_ID_773905,Human_RBP_ID_1093747,Human_RBP_ID_6726568,Human_RBP_ID_22071022,Human_RBP_ID_27270086 55358 RMVar_ID_55358 Human_SNP_ID_660422766 m1A Human chr19 + 18280135 18280135 18280135 CCCCCTCGGAGCCCCCTTCCGCGGCGCGGTGTACAAAGGGGCAGCCGAGACGCGCGGGTTTGTGC CCCCCTCGGAGCCCCCTTCCGCGGCGCGGTGTGCAAAGGGGCAGCCGAGACGCGCGGGTTTGTGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18279701..18280832 26863196 MeRIP-seq:(Medium) rs1342425189 Functional Loss SNV dbSNP153 33..33 33 - - - 55359 RMVar_ID_55359 Human_SNP_ID_660422786 m1A Human chr19 + 18280171 18280171 18280171 AGGGGCAGCCGAGACGCGCGGGTTTGTGCAACACGGGGCGGCCGCGCGGGGGAAAGAGGCAGCGC AGGGGCAGCCGAGACGCGCGGGTTTGTGCAACCCGGGGCGGCCGCGCGGGGGAAAGAGGCAGCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18280076..18280500 26863410 MeRIP-seq:(Medium) rs1205922829 Functional Loss SNV dbSNP153 33..33 33 - - - 55360 RMVar_ID_55360 Human_SNP_ID_660423118 m1A Human chr19 + 18280778 18280778 18280778 GCACCGTCTGTGGCTCGTCCTTGAGCGCAGCCAGGCGCGGCGGCCCCAACGCGCCTGGGGGTGGC GCACCGTCTGTGGCTCGTCCTTGAGCGCAGCCGGGCGCGGCGGCCCCAACGCGCCTGGGGGTGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18280676..18280950 26863410 MeRIP-seq:(Medium) rs760726097 Functional Loss SNV dbSNP153 33..33 33 - - - 55361 RMVar_ID_55361 Human_SNP_ID_660423415 m1A Human chr19 - 18281345 18281343 18281346 CCCGACGGCCGCGGCCGGCAGCATGATGAAGAAGGACGCGCTGACGCTGAGCCTGAGTGAGCAGG CCCGACGGCCGCGGCCGGCAGCATGATGAAG___GACGCGCTGACGCTGAGCCTGAGTGAGCAGG CCTT C JUND Ensembl:ENSG00000130522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:18280062..18281625;chr19:18281007..18281625 26863196 MeRIP-seq:(Medium) rs1205353887 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1556448,Human_RBP_ID_6726597,Human_RBP_ID_8830510,Human_RBP_ID_17935288,Human_RBP_ID_23130815 55362 RMVar_ID_55362 Human_SNP_ID_660423419 m1A Human chr19 + 18281351 18281351 18281351 CACTCAGGCTCAGCGTCAGCGCGTCCTTCTTCATCATGCTGCCGGCCGCGGCCGTCGGGGGCGCC CACTCAGGCTCAGCGTCAGCGCGTCCTTCTTCTTCATGCTGCCGGCCGCGGCCGTCGGGGGCGCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18281017..18281625 26863196 MeRIP-seq:(Medium) rs1287002842 Functional Loss SNV dbSNP153 33..33 33 - - - 55363 RMVar_ID_55363 Human_SNP_ID_660423485 m1A Human chr19 - 18281493 18281493 18281493 GGCCACTCCCCCCCGGGCCGGCGCGGCGGGGGAGGCGGAGGATGGAAACACCCTTCTACGGCGAT GGCCACTCCCCCCCGGGCCGGCGCGGCGGGGGTGGCGGAGGATGGAAACACCCTTCTACGGCGAT T A JUND Ensembl:ENSG00000130522 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:18281451..18281595 26863196 MeRIP-seq:(Medium) rs1031082097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241589,Human_RBP_ID_4557349,Human_RBP_ID_6726601,Human_RBP_ID_8728053 55364 RMVar_ID_55364 Human_SNP_ID_660426960 m1A Human chr19 - 18292668 18292664 18292668 CCCTTTTCAAGGCCGAACCCAGCGCCCACACTAAATGTCAACTCTCCCCATTATCCGGTTGAGGA CCCTTTTCAAGGCCGAACCCAGCGCCCACACT____GTCAACTCTCCCCATTATCCGGTTGAGGA CATTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18292665..18292771 26863196 MeRIP-seq:(Medium) rs1049599768 Functional Loss DEL dbSNP153 33..36 33 - - - 55365 RMVar_ID_55365 Human_SNP_ID_660427753 m1A Human chr19 - 18295516 18295504 18295516 GTGGGTGGGTAGATAGGTGGATGGGTGGATGGATGGGTGGATGGGTGGGTGAGTGGATGGTGGAT GTGGGTGGGTAGATAGGTGGATGGGTGGATGG____________GTGGGTGAGTGGATGGTGGAT CCCATCCACCCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18295513..18295587 26863196 MeRIP-seq:(Medium) rs1219237602 Functional Loss DEL dbSNP153 33..44 33 - - - 55366 RMVar_ID_55366 Human_SNP_ID_660427760 m1A Human chr19 - 18295516 18295515 18295516 GTGGGTGGGTAGATAGGTGGATGGGTGGATGGATGGGTGGATGGGTGGGTGAGTGGATGGTGGAT GTGGGTGGGTAGATAGGTGGATGGGTGGATGG_TGGGTGGATGGGTGGGTGAGTGGATGGTGGAT AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18295513..18295587 26863196 MeRIP-seq:(Medium) rs1488071275 Functional Loss DEL dbSNP153 33..33 33 - - - 55367 RMVar_ID_55367 Human_SNP_ID_660430495 m1A Human chr19 + 18304810 18304810 18304810 GGGTGGGGACCATCTACGATAAAGGCAGCCCCAGTTGGGTGAGGAGGGCACAGACCATCGGAGGG GGGTGGGGACCATCTACGATAAAGGCAGCCCCCGTTGGGTGAGGAGGGCACAGACCATCGGAGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18304807..18304910 26863196 MeRIP-seq:(Medium) rs956486332 Functional Loss SNV dbSNP153 33..33 33 - - - 55368 RMVar_ID_55368 Human_SNP_ID_660431260 m1A Human chr19 + 18307401 18307401 18307401 CCTGCCTCTTCCTTTCTGAGCAGATCCGTCCGAGACTGTGGAGCGGAATCGCCACCCTGGCAGGA CCTGCCTCTTCCTTTCTGAGCAGATCCGTCCGGGACTGTGGAGCGGAATCGCCACCCTGGCAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18307351..18307575 32194978 MeRIP-seq:(Medium) rs1034236775 Functional Loss SNV dbSNP153 33..33 33 - - - 55369 RMVar_ID_55369 Human_SNP_ID_660431307 m1A Human chr19 - 18307492 18307490 18307493 CCCGGGCACAGGCAGAGGCCAGCCAGAGAAGAAGCCTGGCAGACAGGCGGGCAAACAGTGAGCGC CCCGGGCACAGGCAGAGGCCAGCCAGAGAAG___CCTGGCAGACAGGCGGGCAAACAGTGAGCGC GCTT G LSM4 Ensembl:ENSG00000130520 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18307392..18307600 26863410 MeRIP-seq:(Medium) rs758422825 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_204095,Human_RBP_ID_17934914,Human_RBP_ID_22476559 Human_Splice_Rec_1979888,Human_Splice_Rec_1979894,Human_Splice_Rec_1979904 Human_miRNA_ID_2225823 RMVar_hsa_circ_91627,RMVar_hsa_circ_193463 55370 RMVar_ID_55370 Human_SNP_ID_660431308 m1A Human chr19 - 18307492 18307491 18307492 CCCGGGCACAGGCAGAGGCCAGCCAGAGAAGAAGCCTGGCAGACAGGCGGGCAAACAGTGAGCGC CCCGGGCACAGGCAGAGGCCAGCCAGAGAAGA_GCCTGGCAGACAGGCGGGCAAACAGTGAGCGC CT C LSM4 Ensembl:ENSG00000130520 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18307392..18307600 26863410 MeRIP-seq:(Medium) rs777844222 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_204095,Human_RBP_ID_17934914,Human_RBP_ID_22476559 Human_Splice_Rec_1979888,Human_Splice_Rec_1979894,Human_Splice_Rec_1979904 Human_miRNA_ID_2225823 RMVar_hsa_circ_91627,RMVar_hsa_circ_193463 55371 RMVar_ID_55371 Human_SNP_ID_660431335 m1A Human chr19 + 18307552 18307552 18307552 CCGGGATCCCACCTCGGCCCCGGCCACCAAACACACCTAGAGGACAGAGAGAGGGCGCTGCAGCA CCGGGATCCCACCTCGGCCCCGGCCACCAAACGCACCTAGAGGACAGAGAGAGGGCGCTGCAGCA A G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:18307420..18309305 26863410 MeRIP-seq:(Medium) rs1390372200 Functional Loss SNV dbSNP153 33..33 33 - - - 55372 RMVar_ID_55372 Human_SNP_ID_660432894 m1A Human chr19 - 18312625 18312625 18312625 AGCTGCGACAACTGGATGAACATTAACCTGCGAGAAGTCATCTGCACGTCCAGGGTGGGTGCTGC AGCTGCGACAACTGGATGAACATTAACCTGCGCGAAGTCATCTGCACGTCCAGGGTGGGTGCTGC T G LSM4 Ensembl:ENSG00000130520 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs754029923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516142,Human_RBP_ID_1556474,Human_RBP_ID_1881182,Human_RBP_ID_3564550,Human_RBP_ID_3954716,Human_RBP_ID_4510183,Human_RBP_ID_5585473,Human_RBP_ID_8479750,Human_RBP_ID_13394089,Human_RBP_ID_17917138,Human_RBP_ID_18532297,Human_RBP_ID_18724493,Human_RBP_ID_22809829,Human_RBP_ID_23786548,Human_RBP_ID_26334890,Human_RBP_ID_26815531,Human_RBP_ID_27270140 Human_Splice_Rec_1979884,Human_Splice_Rec_1979885,Human_Splice_Rec_1979890,Human_Splice_Rec_1979891,Human_Splice_Rec_1979898,Human_Splice_Rec_1979899,Human_Splice_Rec_1979908,Human_Splice_Rec_1979909,Human_Splice_Rec_1979912,Human_Splice_Rec_1979913,Human_Splice_Rec_1979918 RMVar_hsa_circ_21828 55373 RMVar_ID_55373 Human_SNP_ID_660432911 m1A Human chr19 - 18312671 18312671 18312671 GTTGGTGGAGCTGAAAAATGGGGAGACGTACAATGGACACCTGGTGAGCTGCGACAACTGGATGA GTTGGTGGAGCTGAAAAATGGGGAGACGTACAGTGGACACCTGGTGAGCTGCGACAACTGGATGA T C LSM4 Ensembl:ENSG00000130520 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18312562..18316119 26863196 MeRIP-seq:(Medium) rs1038247251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516145,Human_RBP_ID_1013729,Human_RBP_ID_1556475,Human_RBP_ID_1881183,Human_RBP_ID_3564551,Human_RBP_ID_3954716,Human_RBP_ID_4510186,Human_RBP_ID_6726646,Human_RBP_ID_8479750,Human_RBP_ID_8830517,Human_RBP_ID_9085022,Human_RBP_ID_9329909,Human_RBP_ID_9380803,Human_RBP_ID_13394089,Human_RBP_ID_17267150,Human_RBP_ID_17498235,Human_RBP_ID_17656897,Human_RBP_ID_17917140,Human_RBP_ID_18724494,Human_RBP_ID_23130819,Human_RBP_ID_23786549,Human_RBP_ID_26334890,Human_RBP_ID_26815533 Human_Splice_Rec_1979884,Human_Splice_Rec_1979885,Human_Splice_Rec_1979890,Human_Splice_Rec_1979891,Human_Splice_Rec_1979898,Human_Splice_Rec_1979899,Human_Splice_Rec_1979908,Human_Splice_Rec_1979909,Human_Splice_Rec_1979912,Human_Splice_Rec_1979913,Human_Splice_Rec_1979918 RMVar_hsa_circ_21828 55374 RMVar_ID_55374 Human_SNP_ID_660435558 m1A Human chr19 + 18322956 18322956 18322956 CCGCGCCAACCAAGCCCACAGCGCCCGCCCGCAGGGATCCCAACGACTGCTGTTCCCGCCTCCCG CCGCGCCAACCAAGCCCACAGCGCCCGCCCGCGGGGATCCCAACGACTGCTGTTCCCGCCTCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18322951..18323125 26863196 MeRIP-seq:(Medium) rs1309111317 Functional Loss SNV dbSNP153 33..33 33 - - - 55375 RMVar_ID_55375 Human_SNP_ID_660435654 m1A Human chr19 - 18323067 18323067 18323067 GCGGCGCGGCGACGACCGCCGGGAGCGTGTGCAGCGGCGGCGGCGGAAGTGGCCGGCGAGCCCGG GCGGCGCGGCGACGACCGCCGGGAGCGTGTGCGGCGGCGGCGGCGGAAGTGGCCGGCGAGCCCGG T C LSM4 Ensembl:ENSG00000130520 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18322884..18323125 26863196 MeRIP-seq:(Medium) rs1028020249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516147,Human_RBP_ID_773902,Human_RBP_ID_4510192,Human_RBP_ID_5238717,Human_RBP_ID_5320265,Human_RBP_ID_9328802,Human_RBP_ID_17655327,Human_RBP_ID_18192110,Human_RBP_ID_18421307 Human_Splice_Rec_1979881,Human_Splice_Rec_1979889,Human_Splice_Rec_1979895,Human_Splice_Rec_1979905,Human_Splice_Rec_1979915 55376 RMVar_ID_55376 Human_SNP_ID_660440286 m1A Human chr19 + 18340662 18340662 18340662 CTGTCGCGCCAGTCGCAACAGAAGCAGGTCCGAGGCACAGCCCGATCCCGCCATGGAGCAGCCGA CTGTCGCGCCAGTCGCAACAGAAGCAGGTCCGGGGCACAGCCCGATCCCGCCATGGAGCAGCCGA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18340653..18340764 26863196 MeRIP-seq:(Medium) rs1233856400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557354 Human_Splice_Rec_1979919,Human_Splice_Rec_1979927,Human_Splice_Rec_1979935,Human_Splice_Rec_1979941,Human_Splice_Rec_1979947,Human_Splice_Rec_1979957,Human_Splice_Rec_1979967 55377 RMVar_ID_55377 Human_SNP_ID_660447498 m1A Human chr19 - 18367215 18367215 18367215 TAGCCCCTACCCCAGGCTCTGAAAATGAGGCAAGAGGGAATGGGACTTGGTCCTTCCCTTCTTGC TAGCCCCTACCCCAGGCTCTGAAAATGAGGCAGGAGGGAATGGGACTTGGTCCTTCCCTTCTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18367208..18367447 26863196 MeRIP-seq:(Medium) rs1568323954 Functional Loss SNV dbSNP153 33..33 33 - - - 55378 RMVar_ID_55378 Human_SNP_ID_660447586 m1A Human chr19 - 18367574 18367574 18367574 TTTTGAGCTACATCCCCACACGCATGCAACTGACCTTCTTTGGGGTGGGGAGGGGGTGCTAGGGG TTTTGAGCTACATCCCCACACGCATGCAACTGTCCTTCTTTGGGGTGGGGAGGGGGTGCTAGGGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18367564..18367825 26863196 MeRIP-seq:(Medium) rs1007162077 Functional Loss SNV dbSNP153 33..33 33 - - - 55379 RMVar_ID_55379 Human_SNP_ID_660447601 m1A Human chr19 + 18367633 18367629 18367633 TCAAAAAAGAAATAAGATGGAGTGGAAAGGAAAGAAAGGAAGAAGCAGGAATTCAAGGTGGGTGG TCAAAAAAGAAATAAGATGGAGTGGAAAG____GAAAGGAAGAAGCAGGAATTCAAGGTGGGTGG GGAAA G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:18367596..18367830;chr19:18367602..18367753 26863196 MeRIP-seq:(Medium) rs1432954075 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_21979827,Human_RBP_ID_26472251 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 55380 RMVar_ID_55380 Human_SNP_ID_660453248 m1A Human chr19 + 18388576 18388575 18388576 AGCTGGAGTTGCACTTGCGGCCGCAAGCCGCCAGGGGGCGCCGCAGAGCGCGTGCGCGCAACGGG AGCTGGAGTTGCACTTGCGGCCGCAAGCCGCC_GGGGGCGCCGCAGAGCGCGTGCGCGCAACGGG CA C GDF15 Ensembl:ENSG00000130513 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18388529..18388630 32194978 MeRIP-seq:(Medium) rs767520639 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5145967,Human_RBP_ID_9293536,Human_RBP_ID_18470543,Human_RBP_ID_22070020,Human_RBP_ID_22447572,Human_RBP_ID_22762890 Human_miRNA_ID_2396225,Human_miRNA_ID_2437254 RMVar_hsa_circ_106854,RMVar_hsa_circ_193468 55381 RMVar_ID_55381 Human_SNP_ID_660453448 m1A Human chr19 - 18388927 18388927 18388927 GCACAGTGGAAGGACCAGGACTGCTCATATGCAGTGGCAGTCTTTGGCTAACAAGTCATCATAGG GCACAGTGGAAGGACCAGGACTGCTCATATGCGGTGGCAGTCTTTGGCTAACAAGTCATCATAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18388877..18389027 32194978 MeRIP-seq:(Medium) rs1053471806 Functional Loss SNV dbSNP153 33..33 33 - - - 55382 RMVar_ID_55382 Human_SNP_ID_660461701 m1A Human chr19 - 18419465 18419465 18419465 ACGGCCGCGGCGGCGGCGGCAGCGGCGGCTCCAGCTCCGGCCCCGGCCGCAGGGTGGCTTTTTTT ACGGCCGCGGCGGCGGCGGCAGCGGCGGCTCCTGCTCCGGCCCCGGCCGCAGGGTGGCTTTTTTT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18419376..18426268 26863196 MeRIP-seq:(Medium) rs1204275067 Functional Loss SNV dbSNP153 33..33 33 - - - 55383 RMVar_ID_55383 Human_SNP_ID_660461706 m1A Human chr19 - 18419477 18419468 18419477 GGGGAGCTCCAGACGGCCGCGGCGGCGGCGGCAGCGGCGGCTCCAGCTCCGGCCCCGGCCGCAGG GGGGAGCTCCAGACGGCCGCGGCGGCGGCGGC_________TCCAGCTCCGGCCCCGGCCGCAGG AGCCGCCGCT A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18419426..18419675 26863196 MeRIP-seq:(Medium) rs927477553 Functional Loss DEL dbSNP153 33..41 33 - - - 55384 RMVar_ID_55384 Human_SNP_ID_660461712 m1A Human chr19 - 18419477 18419477 18419477 GGGGAGCTCCAGACGGCCGCGGCGGCGGCGGCAGCGGCGGCTCCAGCTCCGGCCCCGGCCGCAGG GGGGAGCTCCAGACGGCCGCGGCGGCGGCGGCGGCGGCGGCTCCAGCTCCGGCCCCGGCCGCAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18419426..18419675 26863196 MeRIP-seq:(Medium) rs1555720268 Functional Loss SNV dbSNP153 33..33 33 - - - 55385 RMVar_ID_55385 Human_SNP_ID_660462361 m1A Human chr19 - 18421502 18421502 18421502 TCCCGACCGGAGCCTGCCTTCCCGACTGCCACACCCAGGGACACCCAGGGCAGATATGCTGAATC TCCCGACCGGAGCCTGCCTTCCCGACTGCCACGCCCAGGGACACCCAGGGCAGATATGCTGAATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18421497..18421883 26863196 MeRIP-seq:(Medium) rs936419785 Functional Loss SNV dbSNP153 33..33 33 - - - 55386 RMVar_ID_55386 Human_SNP_ID_660463875 m1A Human chr19 - 18427307 18427307 18427307 AGGCGGCCCAGGGAGCTCAGACTCTCCAAGGCAAGGGCCCACCCCAAAGCCCCTCCATCTCTCAG AGGCGGCCCAGGGAGCTCAGACTCTCCAAGGCCAGGGCCCACCCCAAAGCCCCTCCATCTCTCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18427305..18427425 26863196 MeRIP-seq:(Medium) rs1289957759 Functional Loss SNV dbSNP153 33..33 33 - - - 55387 RMVar_ID_55387 Human_SNP_ID_660464103 m1A Human chr19 + 18427932 18427932 18427932 TCTTCTGGGACCTGTACTGCGCGGCGCCTGACAGAAGAGAGGCCTGCGAGCACTCCGGCGAGGCC TCTTCTGGGACCTGTACTGCGCGGCGCCTGACCGAAGAGAGGCCTGCGAGCACTCCGGCGAGGCC A C SSBP4 Ensembl:ENSG00000130511 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18427797..18428022 26863196 MeRIP-seq:(Medium) rs10405636 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1980004,Human_Splice_Rec_1980005,Human_Splice_Rec_1980020,Human_Splice_Rec_1980021,Human_Splice_Rec_1980052,Human_Splice_Rec_1980053,Human_Splice_Rec_1980086,Human_Splice_Rec_1980087,Human_Splice_Rec_1980098,Human_Splice_Rec_1980099,Human_Splice_Rec_1980110,Human_Splice_Rec_1980111,Human_Splice_Rec_1980126,Human_Splice_Rec_1980127,Human_Splice_Rec_1980138,Human_Splice_Rec_1980139,Human_Splice_Rec_1980156,Human_Splice_Rec_1980157 GWAS_ID_6625,GWAS_ID_6626,GWAS_ID_6627,GWAS_ID_6628,GWAS_ID_6629,GWAS_ID_6630 RMVar_hsa_circ_82466,RMVar_hsa_circ_193469 55388 RMVar_ID_55388 Human_SNP_ID_660465484 m1A Human chr19 + 18431658 18431658 18431658 ATCCCCGCCCACCTCTTCCAGCCCTTCATGTCACCGCGCTTCCCAGGGGGCCCCCGGCCCACCCT ATCCCCGCCCACCTCTTCCAGCCCTTCATGTCCCCGCGCTTCCCAGGGGGCCCCCGGCCCACCCT A C SSBP4 Ensembl:ENSG00000130511 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18431626..18431675 26863196 MeRIP-seq:(Medium) rs1195008478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516191,Human_RBP_ID_910992,Human_RBP_ID_4510379,Human_RBP_ID_18192112,Human_RBP_ID_18997194,Human_RBP_ID_23210906 Human_Splice_Rec_1980008,Human_Splice_Rec_1980009,Human_Splice_Rec_1980024,Human_Splice_Rec_1980025,Human_Splice_Rec_1980058,Human_Splice_Rec_1980059,Human_Splice_Rec_1980090,Human_Splice_Rec_1980091,Human_Splice_Rec_1980102,Human_Splice_Rec_1980103,Human_Splice_Rec_1980114,Human_Splice_Rec_1980115,Human_Splice_Rec_1980130,Human_Splice_Rec_1980142,Human_Splice_Rec_1980143,Human_Splice_Rec_1980162,Human_Splice_Rec_1980163 RMVar_hsa_circ_82466,RMVar_hsa_circ_193469 55389 RMVar_ID_55389 Human_SNP_ID_660466105 m1A Human chr19 + 18432953 18432953 18432953 GTGTGTTTGGGGGAAACCCCGTCACACCTGGCACCCTTCTGGTCTCCCCCAGATTCCACCAACTC GTGTGTTTGGGGGAAACCCCGTCACACCTGGCGCCCTTCTGGTCTCCCCCAGATTCCACCAACTC A G SSBP4 Ensembl:ENSG00000130511 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:18432951..18433050;chr19:18432951..18433025 26863196 MeRIP-seq:(Medium) rs1401898474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5370181,Human_RBP_ID_22662374 Human_Splice_Rec_1980039,Human_Splice_Rec_1980073,Human_Splice_Rec_1980197,Human_Splice_Rec_1980209 RMVar_hsa_circ_81738,RMVar_hsa_circ_82466,RMVar_hsa_circ_193469,RMVar_hsa_circ_97227,RMVar_hsa_circ_121279,RMVar_hsa_circ_193471,RMVar_hsa_circ_193472,RMVar_hsa_circ_193473 55390 RMVar_ID_55390 Human_SNP_ID_660466727 m1A Human chr19 - 18433993 18433993 18433993 GGATGGGATCGGGACGGTGAAATAGGAGCGGGAGGTGGTGGGGGGTGGGGAGAGGTTGAGGAGAG GGATGGGATCGGGACGGTGAAATAGGAGCGGGGGGTGGTGGGGGGTGGGGAGAGGTTGAGGAGAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18433976..18434334 26863196 MeRIP-seq:(Medium) rs1292572054 Functional Loss SNV dbSNP153 33..33 33 - - - 55391 RMVar_ID_55391 Human_SNP_ID_660466775 m1A Human chr19 + 18434065 18434065 18434065 CCCCGGGACCCGCGCCCCAGGGCGGCCTTCCCATGCATCGCCCCTCCCCCGTTCCCTCCTGTCCC CCCCGGGACCCGCGCCCCAGGGCGGCCTTCCCCTGCATCGCCCCTCCCCCGTTCCCTCCTGTCCC A C SSBP4 Ensembl:ENSG00000130511 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18434042..18434225 26863196 MeRIP-seq:(Medium) rs558238286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130319,Human_RBP_ID_5320273,Human_RBP_ID_17081768,Human_RBP_ID_17567995,Human_RBP_ID_18945232,Human_RBP_ID_22967726,Human_RBP_ID_25389174,Human_RBP_ID_26785473 RMVar_hsa_circ_81738,RMVar_hsa_circ_121279,RMVar_hsa_circ_193471,RMVar_hsa_circ_193472 55392 RMVar_ID_55392 Human_SNP_ID_660468311 m1A Human chr19 - 18437147 18437147 18437147 AGGTGGGGCCCAGGCCGGGTCGCGGCCCTTTCACCACTCCCACCCGTCACCTCGCCGTGTCTGCT AGGTGGGGCCCAGGCCGGGTCGCGGCCCTTTCTCCACTCCCACCCGTCACCTCGCCGTGTCTGCT T A ISYNA1 Ensembl:ENSG00000105655 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18437145..18437276 26863196 MeRIP-seq:(Medium) rs1181351823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55172,Human_RBP_ID_263227,Human_RBP_ID_3581015,Human_RBP_ID_3954737,Human_RBP_ID_5320276,Human_RBP_ID_5370186,Human_RBP_ID_8100492,Human_RBP_ID_8198700,Human_RBP_ID_8233627,Human_RBP_ID_9426088,Human_RBP_ID_17917203,Human_RBP_ID_19089723,Human_RBP_ID_21977827,Human_RBP_ID_25389200 RMVar_hsa_circ_267052 55393 RMVar_ID_55393 Human_SNP_ID_660469800 m1A Human chr19 + 18441865 18441865 18441865 CAAACTCTGCCTTCTTATCTGGTCCCAGCCAGAGCCCCTGAACAACCCTTTCTCATCATTATGGC CAAACTCTGCCTTCTTATCTGGTCCCAGCCAGGGCCCCTGAACAACCCTTTCTCATCATTATGGC A G AC010335.1 Ensembl:ENSG00000268199 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18441858..18442223 26863196 MeRIP-seq:(Medium) rs994429197 Functional Loss SNV dbSNP153 33..33 33 - - - 55394 RMVar_ID_55394 Human_SNP_ID_660469832 m1A Human chr19 + 18441987 18441985 18441987 AGCCACCACAGAAACCAGGCTGTGACACACCCACACACTACACACACACCCACACCCCAACACAC AGCCACCACAGAAACCAGGCTGTGACACACC__CACACTACACACACACCCACACCCCAACACAC CCA C AC010335.1 Ensembl:ENSG00000268199 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18441977..18442221 26863196 MeRIP-seq:(Medium) rs1385634424 Functional Loss DEL dbSNP153 32..33 33 - - - 55395 RMVar_ID_55395 Human_SNP_ID_660470214 m1A Human chr19 + 18442303 18442291 18442304 ACACCACACACCCCAACACACACCACACCCTCATACCACACACCCAGATACACCACATCCACACA ACACCACACACCCCAACACAC_____________ACCACACACCCAGATACACCACATCCACACA CACCACACCCTCAT C AC010335.1 Ensembl:ENSG00000268199 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18442300..18442398 26863196 MeRIP-seq:(Medium) rs1211588654 Functional Loss DEL dbSNP153 22..34 33 - - - 55396 RMVar_ID_55396 Human_SNP_ID_660470412 m1A Human chr19 + 18442517 18442514 18442517 TAACACATCACACACACTACACACCCACACACAACATCCAACACACACCGACACAGATATACTAC TAACACATCACACACACTACACACCCACAC___ACATCCAACACACACCGACACAGATATACTAC CACA C AC010335.1 Ensembl:ENSG00000268199 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:18442481..18442598;chr19:18441763..18442616 26863196 MeRIP-seq:(Medium) rs1296171819 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_204097 55397 RMVar_ID_55397 Human_SNP_ID_660492455 m1A Human chr19 - 18522027 18522027 18522027 CAAGATGGCGGCGCTGAAGGAGGATAGGAGCTACGGGCTGTCGTGCGGGCGGGTTAGCGACGGCA CAAGATGGCGGCGCTGAAGGAGGATAGGAGCTGCGGGCTGTCGTGCGGGCGGGTTAGCGACGGCA T C ELL Ensembl:ENSG00000105656 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:18521925..18522096;chr19:18521715..18522051 26863196 MeRIP-seq:(Medium) rs758635929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6726850,Human_RBP_ID_18420881,Human_RBP_ID_22977903,Human_RBP_ID_26336048 Human_miRNA_ID_1198827 RMVar_hsa_circ_76677,RMVar_hsa_circ_193476 55398 RMVar_ID_55398 Human_SNP_ID_660495349 m1A Human chr19 - 18531829 18531829 18531829 CTGCCTAGTCCCCGCCTGAGTGCCAGCCCCCCACCCCGCCTGCCGCCCCCTGTCCAGGTTCCCTC CTGCCTAGTCCCCGCCTGAGTGCCAGCCCCCCCCCCCGCCTGCCGCCCCCTGTCCAGGTTCCCTC T G FKBP8 Ensembl:ENSG00000105701 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs867183065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516263,Human_RBP_ID_4510671,Human_RBP_ID_9328827,Human_RBP_ID_17082378,Human_RBP_ID_17387309,Human_RBP_ID_17568512,Human_RBP_ID_18945241 Human_miRNA_ID_1703573 55399 RMVar_ID_55399 Human_SNP_ID_660495657 m1A Human chr19 - 18532758 18532758 18532758 CCACGCAGAGCTCTCAAAGCTGGTGAAGAAGCATGCGGCGCAGCGGAGCACGGAGACCGCCTTGT CCACGCAGAGCTCTCAAAGCTGGTGAAGAAGCGTGCGGCGCAGCGGAGCACGGAGACCGCCTTGT T C FKBP8 Ensembl:ENSG00000105701 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18532634..18532822 26863196 MeRIP-seq:(Medium) rs777128222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1881205,Human_RBP_ID_4564085 Human_Splice_Rec_1980470,Human_Splice_Rec_1980471,Human_Splice_Rec_1980478,Human_Splice_Rec_1980479,Human_Splice_Rec_1980494,Human_Splice_Rec_1980495,Human_Splice_Rec_1980508,Human_Splice_Rec_1980509,Human_Splice_Rec_1980522,Human_Splice_Rec_1980523,Human_Splice_Rec_1980536,Human_Splice_Rec_1980537,Human_Splice_Rec_1980542,Human_Splice_Rec_1980543,Human_Splice_Rec_1980548,Human_Splice_Rec_1980549 RMVar_hsa_circ_45679,RMVar_hsa_circ_45041 55400 RMVar_ID_55400 Human_SNP_ID_660495833 m1A Human chr19 + 18533321 18533321 18533321 TTCAGGGCTGCCCTCAGGATGGGGATGGCCTCACTGTACTCCCCCTGCTGGGCCAGCACCTGTAA TTCAGGGCTGCCCTCAGGATGGGGATGGCCTCGCTGTACTCCCCCTGCTGGGCCAGCACCTGTAA A G AC005387.2 Ensembl:ENSG00000269191 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:18533224..18533388;chr19:18533251..18533350 26863196 MeRIP-seq:(Medium) rs1488183143 Functional Loss SNV dbSNP153 33..33 33 - - - 55401 RMVar_ID_55401 Human_SNP_ID_660497692 m1A Human chr19 + 18539445 18539445 18539445 ATGGCCGTCTCCCCCACGTCCATGAGTGGGACACTGAGATCCAGGGCCTGGGGTGTGTGGGGATA ATGGCCGTCTCCCCCACGTCCATGAGTGGGACGCTGAGATCCAGGGCCTGGGGTGTGTGGGGATA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18538201..18542000 32194978 MeRIP-seq:(Medium) rs1324930774 Functional Loss SNV dbSNP153 33..33 33 - - - 55402 RMVar_ID_55402 Human_SNP_ID_660503288 m1A Human chr19 + 18557913 18557913 18557913 CCCGGAAGCGCGAGCAAGGCCGCCAGATGTGCAGGTGCCGCCGCTACCGACGCCGGGGCCGAGTT CCCGGAAGCGCGAGCAAGGCCGCCAGATGTGCGGGTGCCGCCGCTACCGACGCCGGGGCCGAGTT A G KXD1 Ensembl:ENSG00000105700 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18557801..18558069 26863196 MeRIP-seq:(Medium) rs993937433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773726,Human_RBP_ID_4558262,Human_RBP_ID_5145715,Human_RBP_ID_19092810 Human_Splice_Rec_1980581,Human_Splice_Rec_1980591,Human_Splice_Rec_1980599,Human_Splice_Rec_1980609,Human_Splice_Rec_1980613,Human_Splice_Rec_1980621,Human_Splice_Rec_1980631,Human_Splice_Rec_1980637,Human_Splice_Rec_1980647,Human_Splice_Rec_1980657 55403 RMVar_ID_55403 Human_SNP_ID_660504297 m1A Human chr19 + 18561592 18561592 18561592 GAAATAAAAAAACGAGGTCAAGTAGTAAGAGAAGCGGTAAGAGTGACGGGAACAGGAGTCATTGA GAAATAAAAAAACGAGGTCAAGTAGTAAGAGAGGCGGTAAGAGTGACGGGAACAGGAGTCATTGA A G KXD1 Ensembl:ENSG00000105700 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18561589..18561733 26863196 MeRIP-seq:(Medium) rs952157096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13395383 RMVar_hsa_circ_76805,RMVar_hsa_circ_193493 55404 RMVar_ID_55404 Human_SNP_ID_660505205 m1A Human chr19 + 18564950 18564950 18564950 CTGTCCAGTGCCCGCCTGCAGCAGATGAGCGAACGCTTCCTGCACCACACGAGGACCCTAGTAGA CTGTCCAGTGCCCGCCTGCAGCAGATGAGCGAGCGCTTCCTGCACCACACGAGGACCCTAGTAGA A G KXD1 Ensembl:ENSG00000105700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18564901..18567214 32194978 MeRIP-seq:(Medium) rs758948309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239864,Human_RBP_ID_516309,Human_RBP_ID_770982,Human_RBP_ID_1556522,Human_RBP_ID_1881213,Human_RBP_ID_5190546,Human_RBP_ID_8479874,Human_RBP_ID_18724578,Human_RBP_ID_22065796,Human_RBP_ID_26466061 Human_Splice_Rec_1980586,Human_Splice_Rec_1980587,Human_Splice_Rec_1980594,Human_Splice_Rec_1980595,Human_Splice_Rec_1980604,Human_Splice_Rec_1980605,Human_Splice_Rec_1980616,Human_Splice_Rec_1980617,Human_Splice_Rec_1980624,Human_Splice_Rec_1980625,Human_Splice_Rec_1980634,Human_Splice_Rec_1980635,Human_Splice_Rec_1980640,Human_Splice_Rec_1980641,Human_Splice_Rec_1980650,Human_Splice_Rec_1980651,Human_Splice_Rec_1980662,Human_Splice_Rec_1980666,Human_Splice_Rec_1980667,Human_Splice_Rec_1980674,Human_Splice_Rec_1980675,Human_Splice_Rec_1980684,Human_Splice_Rec_1980685,Human_Splice_Rec_1980690,Human_Splice_Rec_1980691,Human_Splice_Rec_1980694,Human_Splice_Rec_1980695,Human_Splice_Rec_1980700,Human_Splice_Rec_1980701 RMVar_hsa_circ_5481,RMVar_hsa_circ_76805,RMVar_hsa_circ_328397,RMVar_hsa_circ_193493,RMVar_hsa_circ_99149,RMVar_hsa_circ_193496,RMVar_hsa_circ_193494,RMVar_hsa_circ_193495,RMVar_hsa_circ_282027,RMVar_hsa_circ_333045,RMVar_hsa_circ_193497 55405 RMVar_ID_55405 Human_SNP_ID_660506262 m1A Human chr19 + 18568404 18568404 18568404 AAAACCAACTCTTGGGCCTCCTTCCCCCAGATATCCCAGAGGCATCCTTCCTGGAGGAAGAGGAT AAAACCAACTCTTGGGCCTCCTTCCCCCAGATGTCCCAGAGGCATCCTTCCTGGAGGAAGAGGAT A G KXD1 Ensembl:ENSG00000105700 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18568401..18568850 32194978 MeRIP-seq:(Medium) rs1262601400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4510770,Human_RBP_ID_26473774,Human_RBP_ID_27270274 Human_Splice_Rec_1980590,Human_Splice_Rec_1980598,Human_Splice_Rec_1980608,Human_Splice_Rec_1980620,Human_Splice_Rec_1980630,Human_Splice_Rec_1980644,Human_Splice_Rec_1980654,Human_Splice_Rec_1980670,Human_Splice_Rec_1980678,Human_Splice_Rec_1980688,Human_Splice_Rec_1980698,Human_Splice_Rec_1980702 RMVar_hsa_circ_364520 55406 RMVar_ID_55406 Human_SNP_ID_660506263 m1A Human chr19 - 18568405 18568405 18568405 CATCCTCTTCCTCCAGGAAGGATGCCTCTGGGATATCTGGGGGAAGGAGGCCCAAGAGTTGGTTT CATCCTCTTCCTCCAGGAAGGATGCCTCTGGGGTATCTGGGGGAAGGAGGCCCAAGAGTTGGTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18568401..18568500 32194978 MeRIP-seq:(Medium) rs1351432004 Functional Loss SNV dbSNP153 33..33 33 - - - 55407 RMVar_ID_55407 Human_SNP_ID_660506282 m1A Human chr19 - 18568471 18568471 18568471 CACATGAGCCCGTGCTCTGTTCTGAGGTGGCAATGGTGGTCGTGGTGCTGGGTGGGATGGGGTCT CACATGAGCCCGTGCTCTGTTCTGAGGTGGCAGTGGTGGTCGTGGTGCTGGGTGGGATGGGGTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18568421..18568616 26863196 MeRIP-seq:(Medium) rs1390191819 Functional Loss SNV dbSNP153 33..33 33 - - - 55408 RMVar_ID_55408 Human_SNP_ID_660506443 m1A Human chr19 - 18568898 18568898 18568898 AGGCTCAGCTCTGGAAAAATTCCCCTGTGCCCAGCCCCACGACTCCAGCTGGAATGGGCGTGCCC AGGCTCAGCTCTGGAAAAATTCCCCTGTGCCCCGCCCCACGACTCCAGCTGGAATGGGCGTGCCC T G AC005253.2 Ensembl:ENSG00000268983 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18568851..18569040 32194978 MeRIP-seq:(Medium) rs1472460788 Functional Loss SNV dbSNP153 33..33 33 - - - 55409 RMVar_ID_55409 Human_SNP_ID_660507359 m1A Human chr19 - 18571911 18571901 18571911 GCAGCCCCCAACCCGCTCTCGGCCCGGCGCGAACCCGCACGACCGCCGCCACCAACCAGCTCGGC GCAGCCCCCAACCCGCTCTCGGCCCGGCGCGA__________CCGCCGCCACCAACCAGCTCGGC GTCGTGCGGGT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr19:18571826..18572076;chr19:18571876..18571977 26863410,32194978 MeRIP-seq:(Medium) rs1241196874 Functional Loss DEL dbSNP153 33..42 33 - - - 55410 RMVar_ID_55410 Human_SNP_ID_660507360 m1A Human chr19 - 18571902 18571902 18571902 AACCCGCTCTCGGCCCGGCGCGAACCCGCACGACCGCCGCCACCAACCAGCTCGGCCGCCTCGCT AACCCGCTCTCGGCCCGGCGCGAACCCGCACGTCCGCCGCCACCAACCAGCTCGGCCGCCTCGCT T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr19:18571894..18572010;chr19:18571901..18572100 26863196 MeRIP-seq:(Medium) rs911980798 Functional Loss SNV dbSNP153 33..33 33 - - - 55411 RMVar_ID_55411 Human_SNP_ID_660507374 m1A Human chr19 - 18571933 18571933 18571933 GCCCAGGCCCCTGCAGCCTCCCGCAGCCCCCAACCCGCTCTCGGCCCGGCGCGAACCCGCACGAC GCCCAGGCCCCTGCAGCCTCCCGCAGCCCCCAGCCCGCTCTCGGCCCGGCGCGAACCCGCACGAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18571927..18572126 32194978 MeRIP-seq:(Medium) rs1162737695 Functional Loss SNV dbSNP153 33..33 33 - - - 55412 RMVar_ID_55412 Human_SNP_ID_660507613 m1A Human chr19 + 18572725 18572725 18572725 ACTAAGTGATGTTCGTGGTTTGGGGTCAAGGCAAGAAGTGGGGTCTGGAGAGTTTTGGTGTAATT ACTAAGTGATGTTCGTGGTTTGGGGTCAAGGCGAGAAGTGGGGTCTGGAGAGTTTTGGTGTAATT A G UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18572723..18572901 26863196 MeRIP-seq:(Medium) rs1161916814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13395466,Human_RBP_ID_17131763 RMVar_hsa_circ_193498,RMVar_hsa_circ_96992 55413 RMVar_ID_55413 Human_SNP_ID_660507771 m1A Human chr19 - 18573277 18573277 18573277 GATCTGCATGTTTGCGTCTGCAGGAGGAAGGGAGGCAGGATAGACTGGTGAGCAATGCATGCCTG GATCTGCATGTTTGCGTCTGCAGGAGGAAGGGTGGCAGGATAGACTGGTGAGCAATGCATGCCTG T A CRLF1 Ensembl:ENSG00000006016 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:18573276..18573425;chr19:18573276..18573444 26863196 MeRIP-seq:(Medium) rs1402453660 Functional Loss SNV dbSNP153 33..33 33 - - - 55414 RMVar_ID_55414 Human_SNP_ID_660507866 m1A Human chr19 + 18573607 18573607 18573607 CTGGGGGTAGTGCTGGAGCTCCCCTGCAGAGGACACTGCCAGTAATATGGTCCGCAGAGCCTCTA CTGGGGGTAGTGCTGGAGCTCCCCTGCAGAGGCCACTGCCAGTAATATGGTCCGCAGAGCCTCTA A C UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18573600..18573800 26863410 MeRIP-seq:(Medium) rs1007118250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516346,Human_RBP_ID_5370199 RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_278231,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193501,RMVar_hsa_circ_193499 55415 RMVar_ID_55415 Human_SNP_ID_660512584 m1A Human chr19 - 18589604 18589604 18589604 CGGCGAGCAGCGGCTGCCTGCGAGGCCCGCCCAGCTCTGCTTCCACCGCCAGCACCTCCCGCGAG CGGCGAGCAGCGGCTGCCTGCGAGGCCCGCCCTGCTCTGCTTCCACCGCCAGCACCTCCCGCGAG T A CRLF1 Ensembl:ENSG00000006016 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18588776..18589707 26863196 MeRIP-seq:(Medium) rs935074263 Functional Loss SNV dbSNP153 33..33 33 - - - 55416 RMVar_ID_55416 Human_SNP_ID_660513470 m1A Human chr19 + 18592176 18592176 18592176 CCAGGACCTTAGGTTTGATGCGGAATCTGCCGAGTGATGGCGGCTCCCCAGGGATGCGCCGAGGG CCAGGACCTTAGGTTTGATGCGGAATCTGCCGGGTGATGGCGGCTCCCCAGGGATGCGCCGAGGG A G REX1BD Ensembl:ENSG00000006015 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18592126..18592286 32194978 MeRIP-seq:(Medium) rs762178954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516426,Human_RBP_ID_907574,Human_RBP_ID_5116185,Human_RBP_ID_17655331,Human_RBP_ID_17935304,Human_RBP_ID_18165710 Human_Splice_Rec_1980832,Human_Splice_Rec_1980840,Human_Splice_Rec_1980848,Human_Splice_Rec_1980858,Human_Splice_Rec_1980864,Human_Splice_Rec_1980868 55417 RMVar_ID_55417 Human_SNP_ID_660513853 m1A Human chr19 + 18593543 18593543 18593543 GGGTTCGGCCTCTGCGTCTCCACGTGGCAGGGAGGGTGGCCTGAGCCCCTACAGCTTATCTGGCA GGGTTCGGCCTCTGCGTCTCCACGTGGCAGGGGGGGTGGCCTGAGCCCCTACAGCTTATCTGGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18593493..18596972 32194978 MeRIP-seq:(Medium) rs750266467 Functional Loss SNV dbSNP153 33..33 33 - - - 55418 RMVar_ID_55418 Human_SNP_ID_660514307 m1A Human chr19 + 18594745 18594745 18594745 TGGAGTGGGGGGAGGGGAGAATGAGAGAGGCCAGAGCCGGGGGGATGAGACATAGAGATAGACAG TGGAGTGGGGGGAGGGGAGAATGAGAGAGGCCGGAGCCGGGGGGATGAGACATAGAGATAGACAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18594743..18594956 26863196 MeRIP-seq:(Medium) rs950266976 Functional Loss SNV dbSNP153 33..33 33 - - - 55419 RMVar_ID_55419 Human_SNP_ID_660514893 m1A Human chr19 + 18596786 18596786 18596786 GGCGGCAGGAGGTCTGGTTGCTCACATCGTCCACCACCTGGACAGTGAGGACAAGGTCAGAGTAG GGCGGCAGGAGGTCTGGTTGCTCACATCGTCCGCCACCTGGACAGTGAGGACAAGGTCAGAGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr19:18594207..18597069;chr19:18596626..18597009 26863196 MeRIP-seq:(Medium) rs1238787697 Functional Loss SNV dbSNP153 33..33 33 - - - 55420 RMVar_ID_55420 Human_SNP_ID_660515651 m1A Human chr19 - 18598845 18598845 18598845 TCAGCTGCTGGTCCAAGAACATGAAGGACTTGACCTGCCGCTGGACGCCAGGGGCCCACGGGGAG TCAGCTGCTGGTCCAAGAACATGAAGGACTTGGCCTGCCGCTGGACGCCAGGGGCCCACGGGGAG T C CRLF1 Ensembl:ENSG00000006016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18598745..18598938 26863196 MeRIP-seq:(Medium) rs758469818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22447592,Human_RBP_ID_22764006 Human_Splice_Rec_1980808,Human_Splice_Rec_1980809 RMVar_hsa_circ_126318,RMVar_hsa_circ_193509,RMVar_hsa_circ_89748,RMVar_hsa_circ_193511,RMVar_hsa_circ_118825,RMVar_hsa_circ_362274,RMVar_hsa_circ_193512 55421 RMVar_ID_55421 Human_SNP_ID_660515652 m1A Human chr19 - 18598845 18598845 18598845 TCAGCTGCTGGTCCAAGAACATGAAGGACTTGACCTGCCGCTGGACGCCAGGGGCCCACGGGGAG TCAGCTGCTGGTCCAAGAACATGAAGGACTTGCCCTGCCGCTGGACGCCAGGGGCCCACGGGGAG T G CRLF1 Ensembl:ENSG00000006016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18598745..18598938 26863196 MeRIP-seq:(Medium) rs758469818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22447592,Human_RBP_ID_22764006 Human_Splice_Rec_1980808,Human_Splice_Rec_1980809 RMVar_hsa_circ_126318,RMVar_hsa_circ_193509,RMVar_hsa_circ_89748,RMVar_hsa_circ_193511,RMVar_hsa_circ_118825,RMVar_hsa_circ_362274,RMVar_hsa_circ_193512 55422 RMVar_ID_55422 Human_SNP_ID_660515982 m1A Human chr19 + 18599799 18599799 18599799 GTCTCCGTGCACTGAGCAGGTGGCCAGCAGGGAGGAGCCGATGAGAAGCGTGGGATCCTGGGGAC GTCTCCGTGCACTGAGCAGGTGGCCAGCAGGGGGGAGCCGATGAGAAGCGTGGGATCCTGGGGAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18599651..18599850 26863196 MeRIP-seq:(Medium) rs763900232 Functional Loss SNV dbSNP153 33..33 33 - - - 55423 RMVar_ID_55423 Human_SNP_ID_660515984 m1A Human chr19 + 18599802 18599802 18599802 TCCGTGCACTGAGCAGGTGGCCAGCAGGGAGGAGCCGATGAGAAGCGTGGGATCCTGGGGACTGA TCCGTGCACTGAGCAGGTGGCCAGCAGGGAGGTGCCGATGAGAAGCGTGGGATCCTGGGGACTGA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18599751..18599925 26863196 MeRIP-seq:(Medium) rs1568441784 Functional Loss SNV dbSNP153 33..33 33 - - - 55424 RMVar_ID_55424 Human_SNP_ID_660517878 m1A Human chr19 + 18606510 18606510 18606510 CTGCCCCCGGGGCGCCCGCCCTCTGCTCTGGCAGGGGGGAAGGAGTGGGGCGCCGGGTACTCACG CTGCCCCCGGGGCGCCCGCCCTCTGCTCTGGCCGGGGGGAAGGAGTGGGGCGCCGGGTACTCACG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:18606507..18606781 26863196 MeRIP-seq:(Medium) rs565524847 Functional Loss SNV dbSNP153 33..33 33 - - - 55425 RMVar_ID_55425 Human_SNP_ID_660517885 m1A Human chr19 - 18606523 18606523 18606523 CGGATCAGGAGCCCGTGAGTACCCGGCGCCCCACTCCTTCCCCCCTGCCAGAGCAGAGGGCGGGC CGGATCAGGAGCCCGTGAGTACCCGGCGCCCCGCTCCTTCCCCCCTGCCAGAGCAGAGGGCGGGC T C CRLF1 Ensembl:ENSG00000006016 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18606517..18606685 26863196 MeRIP-seq:(Medium) rs1334793935 Functional Loss SNV dbSNP153 33..33 33 - - - 55426 RMVar_ID_55426 Human_SNP_ID_660517957 m1A Human chr19 + 18606739 18606729 18606739 GCGCAGGGCGCGGGACGCAGGCCGGGCGCGGGAGGGCGCGGGCCAGGCCGCCCGCACGTCGCTGG GCGCAGGGCGCGGGACGCAGGCC__________GGGCGCGGGCCAGGCCGCCCGCACGTCGCTGG CGGGCGCGGGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18606704..18606779 26863196 MeRIP-seq:(Medium) rs1170307260 Functional Loss DEL dbSNP153 24..33 33 - - - 55427 RMVar_ID_55427 Human_SNP_ID_660519604 m1A Human chr19 - 18613002 18613002 18613002 GCGCGGAGGCGGCGGGCGGCGACGCCAACAGCAGCAGCAGCAGCAGCGGCGGTGGCATCAGCGCC GCGCGGAGGCGGCGGGCGGCGACGCCAACAGCCGCAGCAGCAGCAGCGGCGGTGGCATCAGCGCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18612901..18613125 26863410 MeRIP-seq:(Medium) rs888829119 Functional Loss SNV dbSNP153 33..33 33 - - - 55428 RMVar_ID_55428 Human_SNP_ID_660526227 m1A Human chr19 - 18637090 18637090 18637090 GGGCCCGGGCCCGCGCCGAAAGCGCCGCCGCCACCAGCACCACCGCTGCTACCGCCGGACTCCGC GGGCCCGGGCCCGCGCCGAAAGCGCCGCCGCCCCCAGCACCACCGCTGCTACCGCCGGACTCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18637057..18637189 26863196 MeRIP-seq:(Medium) rs995387678 Functional Loss SNV dbSNP153 33..33 33 - - - 55429 RMVar_ID_55429 Human_SNP_ID_660526291 m1A Human chr19 + 18637295 18637295 18637295 TTGGACTTTACGGGGCCGTGGGGTACTGGAGGAGCCGAGGGCTACTGAGGGGGTGGCTGGAGGGG TTGGACTTTACGGGGCCGTGGGGTACTGGAGGGGCCGAGGGCTACTGAGGGGGTGGCTGGAGGGG A G KLHL26 Ensembl:ENSG00000167487 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18637246..18637454 26863196 MeRIP-seq:(Medium) rs1185232918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3586177,Human_RBP_ID_6727048 55430 RMVar_ID_55430 Human_SNP_ID_660526369 m1A Human chr19 - 18637596 18637596 18637596 CTTCCAGCGCCCCTCAGCACGCTCTCAGGACCACCTTTAGCCACCTTGGGGCCCTTCAGCACCTC CTTCCAGCGCCCCTCAGCACGCTCTCAGGACCCCCTTTAGCCACCTTGGGGCCCTTCAGCACCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18637547..18637642 26863196 MeRIP-seq:(Medium) rs887394536 Functional Loss SNV dbSNP153 33..33 33 - - - 55431 RMVar_ID_55431 Human_SNP_ID_660528833 m1A Human chr19 + 18647566 18647564 18647567 GAAGAGAGGAGGAGGAGGAAGAGTGGAGGAAGAGGAGGAGGAGATGAGAGGGAGGAGGAGGAAGA GAAGAGAGGAGGAGGAGGAAGAGTGGAGGAA___GAGGAGGAGATGAGAGGGAGGAGGAGGAAGA AGAG A KLHL26 Ensembl:ENSG00000167487 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18647558..18647782 26863196 MeRIP-seq:(Medium) rs1258513914 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2559325 55432 RMVar_ID_55432 Human_SNP_ID_660528856 m1A Human chr19 + 18647638 18647622 18647639 GAGAAAAAGAGGAGGAAGAGGAGGAGGAAGAGAGGAGGAGGAGGAAAGAGAGAGGAGGAGAAAAA GAGAAAAAGAGGAGGAA_________________GAGGAGGAGGAAAGAGAGAGGAGGAGAAAAA AGAGGAGGAGGAAGAGAG A KLHL26 Ensembl:ENSG00000167487 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18647630..18647758 26863196 MeRIP-seq:(Medium) rs1190396384 Functional Loss DEL dbSNP153 18..34 33 - - - 55433 RMVar_ID_55433 Human_SNP_ID_660531776 m1A Human chr19 - 18658518 18658517 18658519 ACAGAGACCCAGGGAGAGAGGGAGAGGGAGAGACAGAGACCCAGAGACAGGGAGACAGAGACCCA ACAGAGACCCAGGGAGAGAGGGAGAGGGAGA__CAGAGACCCAGAGACAGGGAGACAGAGACCCA GTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18658511..18658577 26863196 MeRIP-seq:(Medium) rs1408826132 Functional Loss DEL dbSNP153 32..33 33 - - - 55434 RMVar_ID_55434 Human_SNP_ID_660531778 m1A Human chr19 - 18658518 18658518 18658518 ACAGAGACCCAGGGAGAGAGGGAGAGGGAGAGACAGAGACCCAGAGACAGGGAGACAGAGACCCA ACAGAGACCCAGGGAGAGAGGGAGAGGGAGAGGCAGAGACCCAGAGACAGGGAGACAGAGACCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18658511..18658577 26863196 MeRIP-seq:(Medium) rs1339263741 Functional Loss SNV dbSNP153 33..33 33 - - - 55435 RMVar_ID_55435 Human_SNP_ID_660533251 m1A Human chr19 + 18664307 18664307 18664307 ACGGGGCCCTCAAGTGCACCTTCTCGGCACCCAGCCACAGCACCAGCCTCCTGCAGGGCCTGGCC ACGGGGCCCTCAAGTGCACCTTCTCGGCACCCGGCCACAGCACCAGCCTCCTGCAGGGCCTGGCC A G KLHL26 Ensembl:ENSG00000167487 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18664219..18664373 26863196 MeRIP-seq:(Medium) rs528946301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1980926,Human_Splice_Rec_1980932,Human_Splice_Rec_1980936,Human_Splice_Rec_1980942,Human_Splice_Rec_1980946,Human_Splice_Rec_1980950 Human_miRNA_ID_272536,Human_miRNA_ID_1036082,Human_miRNA_ID_1395917 55436 RMVar_ID_55436 Human_SNP_ID_660533254 m1A Human chr19 + 18664313 18664313 18664313 CCCTCAAGTGCACCTTCTCGGCACCCAGCCACAGCACCAGCCTCCTGCAGGGCCTGGCCACCCTC CCCTCAAGTGCACCTTCTCGGCACCCAGCCACGGCACCAGCCTCCTGCAGGGCCTGGCCACCCTC A G KLHL26 Ensembl:ENSG00000167487 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18664230..18664346 26863196 MeRIP-seq:(Medium) rs757318991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1980926,Human_Splice_Rec_1980932,Human_Splice_Rec_1980936,Human_Splice_Rec_1980942,Human_Splice_Rec_1980946,Human_Splice_Rec_1980950 Human_miRNA_ID_272536,Human_miRNA_ID_1036082,Human_miRNA_ID_1395917 55437 RMVar_ID_55437 Human_SNP_ID_660534678 m1A Human chr19 - 18668509 18668509 18668509 CGTCCACTGCGCCCTCGCCGCTGCGGTACTGCAGGTGCTGCCCCCCGGCCACGTACACAAAATTG CGTCCACTGCGCCCTCGCCGCTGCGGTACTGCTGGTGCTGCCCCCCGGCCACGTACACAAAATTG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18668166..18668517 32194978 MeRIP-seq:(Medium) rs1263045227 Functional Loss SNV dbSNP153 33..33 33 - - - 55438 RMVar_ID_55438 Human_SNP_ID_660535104 m1A Human chr19 + 18669305 18669305 18669305 GACCGCATGTTGTCTCCAAGTGGGGCTTGGCGAATGCACGTCTGCCTGAGAACCCCAGTGCCCCC GACCGCATGTTGTCTCCAAGTGGGGCTTGGCGGATGCACGTCTGCCTGAGAACCCCAGTGCCCCC A G KLHL26 Ensembl:ENSG00000167487 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18669265..18669366 26863196 MeRIP-seq:(Medium) rs767888084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1980940 RMVar_hsa_circ_266624 55439 RMVar_ID_55439 Human_SNP_ID_660538821 m1A Human chr19 - 18683720 18683720 18683720 TGCAGCGCGATCTTCTCGCTGAATTTCCGCGGATTGTTCGAAGTCGCCATCTTCTCGCCGCCACC TGCAGCGCGATCTTCTCGCTGAATTTCCGCGGGTTGTTCGAAGTCGCCATCTTCTCGCCGCCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18683671..18683805 26863196 MeRIP-seq:(Medium) rs1379086459 Functional Loss SNV dbSNP153 33..33 33 - - - 55440 RMVar_ID_55440 Human_SNP_ID_660538822 m1A Human chr19 - 18683720 18683720 18683720 TGCAGCGCGATCTTCTCGCTGAATTTCCGCGGATTGTTCGAAGTCGCCATCTTCTCGCCGCCACC TGCAGCGCGATCTTCTCGCTGAATTTCCGCGGCTTGTTCGAAGTCGCCATCTTCTCGCCGCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18683671..18683805 26863196 MeRIP-seq:(Medium) rs1379086459 Functional Loss SNV dbSNP153 33..33 33 - - - 55441 RMVar_ID_55441 Human_SNP_ID_660538839 m1A Human chr19 + 18683814 18683814 18683814 CCTTCGAGGAGGTCATGAAGGACCTGAGCCTGACGCGGGCCGCGCGGGTAAGGGGGCTGCCCGCG CCTTCGAGGAGGTCATGAAGGACCTGAGCCTGTCGCGGGCCGCGCGGGTAAGGGGGCTGCCCGCG A T CRTC1 Ensembl:ENSG00000105662 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr19:18683810..18683948;chr19:18683775..18742972 26863196,32194978 MeRIP-seq:(Medium) rs1180453611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911016,Human_RBP_ID_9380807,Human_RBP_ID_18421315,Human_RBP_ID_18997245,Human_RBP_ID_26336054,Human_RBP_ID_27815325 Human_Splice_Rec_1980953,Human_Splice_Rec_1980979 55442 RMVar_ID_55442 Human_SNP_ID_660542357 m1A Human chr19 - 18696250 18696250 18696250 CAGGCTTCCAGCAGCCTGAACCGCCCTGCCTCACCCTGACCAGCCGGCCAACTCCCAGAACTCCG CAGGCTTCCAGCAGCCTGAACCGCCCTGCCTCCCCCTGACCAGCCGGCCAACTCCCAGAACTCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18696245..18696372 26863196 MeRIP-seq:(Medium) rs1161211413 Functional Loss SNV dbSNP153 33..33 33 - - - 55443 RMVar_ID_55443 Human_SNP_ID_660548385 m1A Human chr19 - 18718977 18718977 18718977 GGCCTCCCTGCTCCCTCTGCAAGTGGCTGCCGAGACTCCTTCATTTTCTTCTCTTTATTCATTCA GGCCTCCCTGCTCCCTCTGCAAGTGGCTGCCGGGACTCCTTCATTTTCTTCTCTTTATTCATTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18718965..18719102 26863196 MeRIP-seq:(Medium) rs79339005 Functional Loss SNV dbSNP153 33..33 33 - - - 55444 RMVar_ID_55444 Human_SNP_ID_660555850 m1A Human chr19 - 18745916 18745916 18745916 TTTGTCCACTGACAGGGGCCGGCGGTGTGGGGAGCCGAGCCGGCCACGCTCCCGGTACACCCTGT TTTGTCCACTGACAGGGGCCGGCGGTGTGGGGTGCCGAGCCGGCCACGCTCCCGGTACACCCTGT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18745868..18747060 26863196 MeRIP-seq:(Medium) rs775233461 Functional Loss SNV dbSNP153 33..33 33 - - - 55445 RMVar_ID_55445 Human_SNP_ID_660559953 m1A Human chr19 + 18760036 18760036 18760036 CCAGCATCTTCCCGTCTGCCGACCAGGAAAACACTACAGCCCTGATCCCCGCCACCCACAACACA CCAGCATCTTCCCGTCTGCCGACCAGGAAAACGCTACAGCCCTGATCCCCGCCACCCACAACACA A G CRTC1 Ensembl:ENSG00000105662 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18760004..18760151 26863196 MeRIP-seq:(Medium) rs1169114463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911019 Human_Splice_Rec_1980966,Human_Splice_Rec_1980990,Human_Splice_Rec_1981014,Human_Splice_Rec_1981036 RMVar_hsa_circ_5218,RMVar_hsa_circ_193519,RMVar_hsa_circ_117412,RMVar_hsa_circ_369411,RMVar_hsa_circ_193518 55446 RMVar_ID_55446 Human_SNP_ID_660562361 m1A Human chr19 - 18768510 18768510 18768510 GGGTGAAGAAGGCGTAGGGCAGCTGCTGCTCCAGAGACAGGGCGTCCATGGCTACAGCCTGCAGG GGGTGAAGAAGGCGTAGGGCAGCTGCTGCTCCGGAGACAGGGCGTCCATGGCTACAGCCTGCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18768504..18768585 26863196 MeRIP-seq:(Medium) rs1487158056 Functional Loss SNV dbSNP153 33..33 33 - - - 55447 RMVar_ID_55447 Human_SNP_ID_660562396 m1A Human chr19 - 18768592 18768591 18768592 GGCGGGGGTGGTGGCTGCTGGGACGCGGGTGGAGGAGGCGGCGGGGGCTGGGGCTGCGGCGGTGG GGCGGGGGTGGTGGCTGCTGGGACGCGGGTGG_GGAGGCGGCGGGGGCTGGGGCTGCGGCGGTGG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18765502..18771456 26863196 MeRIP-seq:(Medium) rs1426596284 Functional Loss DEL dbSNP153 33..33 33 - - - 55448 RMVar_ID_55448 Human_SNP_ID_660563118 m1A Human chr19 - 18770907 18770906 18770908 ACACAGGCACACATCCACACACAAACGTACATACCCACAAATGCACACATGCACACAAATGTACA ACACAGGCACACATCCACACACAAACGTACA__CCCACAAATGCACACATGCACACAAATGTACA GTA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:18770896..18771096 26863196 MeRIP-seq:(Medium) rs1222887229 Functional Loss DEL dbSNP153 32..33 33 - - - 55449 RMVar_ID_55449 Human_SNP_ID_660563119 m1A Human chr19 - 18770907 18770907 18770907 ACACAGGCACACATCCACACACAAACGTACATACCCACAAATGCACACATGCACACAAATGTACA ACACAGGCACACATCCACACACAAACGTACATGCCCACAAATGCACACATGCACACAAATGTACA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:18770896..18771096 26863196 MeRIP-seq:(Medium) rs1181162381 Functional Loss SNV dbSNP153 33..33 33 - - - 55450 RMVar_ID_55450 Human_SNP_ID_660565019 m1A Human chr19 + 18777258 18777258 18777258 GGTCGGCGACGTCAGCTTCGACTCCGACAGCCAGTTTCCCCTGGACGAACTCAAGATCGACCCCC GGTCGGCGACGTCAGCTTCGACTCCGACAGCCGGTTTCCCCTGGACGAACTCAAGATCGACCCCC A G CRTC1 Ensembl:ENSG00000105662 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18777208..18777657 26863196 MeRIP-seq:(Medium) rs201237421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9382313,Human_RBP_ID_13396588 Human_Splice_Rec_1980978,Human_Splice_Rec_1981002,Human_Splice_Rec_1981026,Human_Splice_Rec_1981042 55451 RMVar_ID_55451 Human_SNP_ID_660565118 m1A Human chr19 - 18777448 18777448 18777448 TCACAAGCTCGGCCGTTGGCGAGGGACGGAGCACGGCCGTCCCCGGGCTGGGGAGGCGCCGTCGG TCACAAGCTCGGCCGTTGGCGAGGGACGGAGCGCGGCCGTCCCCGGGCTGGGGAGGCGCCGTCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18777346..18777467 26863410 MeRIP-seq:(Medium) rs1201953938 Functional Loss SNV dbSNP153 33..33 33 - - - 55452 RMVar_ID_55452 Human_SNP_ID_660565128 m1A Human chr19 + 18777465 18777465 18777465 GCCCGGGGACGGCCGTGCTCCGTCCCTCGCCAACGGCCGAGCTTGTGATTCTGAGCTTGCAATGC GCCCGGGGACGGCCGTGCTCCGTCCCTCGCCAGCGGCCGAGCTTGTGATTCTGAGCTTGCAATGC A G CRTC1 Ensembl:ENSG00000105662 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18777258..18777906 32194978 MeRIP-seq:(Medium) rs1053438863 Functional Loss SNV dbSNP153 33..33 33 - - - 55453 RMVar_ID_55453 Human_SNP_ID_660565284 m1A Human chr19 - 18777795 18777792 18777796 GGGAACCAAGGAAGGCAGTGAGAGCTGGACAAACAGTCGGAAAATGCGCCACGGCCCACAGCCCT GGGAACCAAGGAAGGCAGTGAGAGCTGGACA____GTCGGAAAATGCGCCACGGCCCACAGCCCT CTGTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18777744..18777837 26863196 MeRIP-seq:(Medium) rs769040683 Functional Loss DEL dbSNP153 32..35 33 - - - 55454 RMVar_ID_55454 Human_SNP_ID_660581270 m1A Human chr19 + 18832045 18832045 18832045 GAGGGGCTCGGCGGCAGCGGCGGCGGCTCGGCACTGTTACCTCTCGGTCCGGCTGGCGCCGGGGC GAGGGGCTCGGCGGCAGCGGCGGCGGCTCGGCGCTGTTACCTCTCGGTCCGGCTGGCGCCGGGGC A G UPF1 Ensembl:ENSG00000005007 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:18831950..18832081 26863196 MeRIP-seq:(Medium) rs1304403918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558269,Human_RBP_ID_5421273,Human_RBP_ID_9293562,Human_RBP_ID_18420883 55455 RMVar_ID_55455 Human_SNP_ID_660581426 m1A Human chr19 - 18832442 18832442 18832442 GCCCGGGCTTCCGGCACCGCCATGTGCCGCTCACCTGCGCGTCGAGCTGTCCCGCCGCAGCGCCC GCCCGGGCTTCCGGCACCGCCATGTGCCGCTCCCCTGCGCGTCGAGCTGTCCCGCCGCAGCGCCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18832401..18832450 32194978 MeRIP-seq:(Medium) rs1046527255 Functional Loss SNV dbSNP153 33..33 33 - - - 55456 RMVar_ID_55456 Human_SNP_ID_660583347 m1A Human chr19 - 18840030 18840030 18840030 CACCCCAGCAGCTCCTAAAGGCTCCAGGACACAGCCCAGCCCCTGCCCTGGCCCCACTGGCCCCA CACCCCAGCAGCTCCTAAAGGCTCCAGGACACGGCCCAGCCCCTGCCCTGGCCCCACTGGCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18840023..18840252 26863196 MeRIP-seq:(Medium) rs1278955514 Functional Loss SNV dbSNP153 33..33 33 - - - 55457 RMVar_ID_55457 Human_SNP_ID_660583952 m1A Human chr19 + 18842347 18842347 18842347 TTAACCAACAGTGTGGCAGGCTGGGTGCGCTCATGAGCCAGCTGTTTTGTGGGGATGTGGAGAAA TTAACCAACAGTGTGGCAGGCTGGGTGCGCTCGTGAGCCAGCTGTTTTGTGGGGATGTGGAGAAA A G UPF1 Ensembl:ENSG00000005007 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18842340..18842438 26863196 MeRIP-seq:(Medium) rs933818721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23787061 55458 RMVar_ID_55458 Human_SNP_ID_660590088 m1A Human chr19 + 18863577 18863577 18863577 TCAACAACCTGCGTGAGAGCCTCATGCAGTTCAGCAAGCCACGGAAGCTGGTCAACACTATCAAC TCAACAACCTGCGTGAGAGCCTCATGCAGTTCCGCAAGCCACGGAAGCTGGTCAACACTATCAAC A C UPF1 Ensembl:ENSG00000005007 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18863526..18863625 32194978 MeRIP-seq:(Medium) rs1387502502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3956614 Human_Splice_Rec_1981187,Human_Splice_Rec_1981231,Human_Splice_Rec_1981297,Human_Splice_Rec_1981305 Human_miRNA_ID_2027624 RMVar_hsa_circ_50109,RMVar_hsa_circ_357694,RMVar_hsa_circ_91025,RMVar_hsa_circ_96784,RMVar_hsa_circ_193525,RMVar_hsa_circ_193527,RMVar_hsa_circ_353670,RMVar_hsa_circ_122007,RMVar_hsa_circ_193531,RMVar_hsa_circ_193532,RMVar_hsa_circ_83983,RMVar_hsa_circ_345702,RMVar_hsa_circ_289882,RMVar_hsa_circ_193536,RMVar_hsa_circ_193537 55459 RMVar_ID_55459 Human_SNP_ID_660590807 m1A Human chr19 + 18865658 18865658 18865658 GGACCCAGCCAGACTAACCTCCCCAACAGCCAAGCCAGCCAGGATGTGGCGTCACAGCCCTTCTC GGACCCAGCCAGACTAACCTCCCCAACAGCCAGGCCAGCCAGGATGTGGCGTCACAGCCCTTCTC A G UPF1 Ensembl:ENSG00000005007 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18865609..18865709 26863196 MeRIP-seq:(Medium) rs946917628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18192973,Human_RBP_ID_23211233 Human_Splice_Rec_1981192,Human_Splice_Rec_1981236,Human_Splice_Rec_1981302 Human_miRNA_ID_794342,Human_miRNA_ID_2333310,Human_miRNA_ID_2966393 RMVar_hsa_circ_96784,RMVar_hsa_circ_193527,RMVar_hsa_circ_122007,RMVar_hsa_circ_193532 55460 RMVar_ID_55460 Human_SNP_ID_660590969 m1A Human chr19 + 18866165 18866165 18866165 TGGCGGGGTGACGGGGCTGTCCCAGTATTAAAAGGCAAGCCCCCCTGGAGCAGGCCTGGCCCCAC TGGCGGGGTGACGGGGCTGTCCCAGTATTAAAGGGCAAGCCCCCCTGGAGCAGGCCTGGCCCCAC A G UPF1 Ensembl:ENSG00000005007 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18866126..18866175 32194978 MeRIP-seq:(Medium) rs1289305021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19089767,Human_RBP_ID_23257753 RMVar_hsa_circ_96784,RMVar_hsa_circ_193527,RMVar_hsa_circ_122007,RMVar_hsa_circ_193532 55461 RMVar_ID_55461 Human_SNP_ID_660591699 m1A Human chr19 - 18868063 18868063 18868063 GGCGAAGCAGAGGCAAAGCGGCCCAGCCCAACAGCCGGGATGGGGCAGGGAGCGTCCCTCAGGCC GGCGAAGCAGAGGCAAAGCGGCCCAGCCCAACTGCCGGGATGGGGCAGGGAGCGTCCCTCAGGCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18867851..18868200 32194978 MeRIP-seq:(Medium) rs1487880761 Functional Loss SNV dbSNP153 33..33 33 - - - 55462 RMVar_ID_55462 Human_SNP_ID_660591700 m1A Human chr19 - 18868063 18868063 18868063 GGCGAAGCAGAGGCAAAGCGGCCCAGCCCAACAGCCGGGATGGGGCAGGGAGCGTCCCTCAGGCC GGCGAAGCAGAGGCAAAGCGGCCCAGCCCAACGGCCGGGATGGGGCAGGGAGCGTCCCTCAGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18867851..18868200 32194978 MeRIP-seq:(Medium) rs1487880761 Functional Loss SNV dbSNP153 33..33 33 - - - 55463 RMVar_ID_55463 Human_SNP_ID_660592691 m1A Human chr19 + 18870216 18870216 18870216 CCTGGAGCAGGGCGGCGGCTGGGCCTGGGGGCACGGGGGCGCGGGTCAGGGGCAGCGAGGGCAGC CCTGGAGCAGGGCGGCGGCTGGGCCTGGGGGCGCGGGGGCGCGGGTCAGGGGCAGCGAGGGCAGC A G NONHSAG025150.2 RNACentral:URS00008B4C8E lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18870123..18870272 26863410 MeRIP-seq:(Medium) rs1568291627 Functional Loss SNV dbSNP153 33..33 33 - - - 55464 RMVar_ID_55464 Human_SNP_ID_660593768 m1A Human chr19 - 18873949 18873949 18873949 TCCTGGGTCCTCCTCAAACCCAGCTGTGCCCCATCTTCCTCCCCCCATCCCGAAGACCACTCCTG TCCTGGGTCCTCCTCAAACCCAGCTGTGCCCCGTCTTCCTCCCCCCATCCCGAAGACCACTCCTG T C GDF1,CERS1 Ensembl:ENSG00000130283,Ensembl:ENSG00000223802 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18873944..18874015 26863196 MeRIP-seq:(Medium) rs1352991745 Functional Loss SNV dbSNP153 33..33 33 - - - 55465 RMVar_ID_55465 Human_SNP_ID_660599247 m1A Human chr19 + 18893508 18893508 18893508 CACTGTAGCTCCAGCTGCCCAGGTAGAAGAGAAACTTCCAAGCGCTCTCGGGCATCTTGGCGGCA CACTGTAGCTCCAGCTGCCCAGGTAGAAGAGACACTTCCAAGCGCTCTCGGGCATCTTGGCGGCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18884124..18895925 32194978 MeRIP-seq:(Medium) rs1489696928 Functional Loss SNV dbSNP153 33..33 33 - - - 55466 RMVar_ID_55466 Human_SNP_ID_660601339 m1A Human chr19 - 18900435 18900435 18900435 GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCAGAGACGCTGGTCAACCTCATCGTCCTGTCCCA GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCTGAGACGCTGGTCAACCTCATCGTCCTGTCCCA T A COPE Ensembl:ENSG00000105669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18899957..18903468 26863196 MeRIP-seq:(Medium) rs1127821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53434,Human_RBP_ID_22476571,Human_RBP_ID_22762897 Human_Splice_Rec_1981398,Human_Splice_Rec_1981399,Human_Splice_Rec_1981414,Human_Splice_Rec_1981415,Human_Splice_Rec_1981420,Human_Splice_Rec_1981421,Human_Splice_Rec_1981440,Human_Splice_Rec_1981441,Human_Splice_Rec_1981454,Human_Splice_Rec_1981455,Human_Splice_Rec_1981470,Human_Splice_Rec_1981471,Human_Splice_Rec_1981482,Human_Splice_Rec_1981483 GWAS_ID_6631 RMVar_hsa_circ_193546,RMVar_hsa_circ_109918,RMVar_hsa_circ_86189,RMVar_hsa_circ_96801,RMVar_hsa_circ_193545,RMVar_hsa_circ_344320,RMVar_hsa_circ_193547,RMVar_hsa_circ_62378 55467 RMVar_ID_55467 Human_SNP_ID_660601340 m1A Human chr19 - 18900435 18900435 18900435 GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCAGAGACGCTGGTCAACCTCATCGTCCTGTCCCA GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCGGAGACGCTGGTCAACCTCATCGTCCTGTCCCA T C COPE Ensembl:ENSG00000105669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18899957..18903468 26863196 MeRIP-seq:(Medium) rs1127821 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_53434,Human_RBP_ID_22476571,Human_RBP_ID_22762897 Human_Splice_Rec_1981398,Human_Splice_Rec_1981399,Human_Splice_Rec_1981414,Human_Splice_Rec_1981415,Human_Splice_Rec_1981420,Human_Splice_Rec_1981421,Human_Splice_Rec_1981440,Human_Splice_Rec_1981441,Human_Splice_Rec_1981454,Human_Splice_Rec_1981455,Human_Splice_Rec_1981470,Human_Splice_Rec_1981471,Human_Splice_Rec_1981482,Human_Splice_Rec_1981483 GWAS_ID_6631 RMVar_hsa_circ_193546,RMVar_hsa_circ_109918,RMVar_hsa_circ_86189,RMVar_hsa_circ_96801,RMVar_hsa_circ_193545,RMVar_hsa_circ_344320,RMVar_hsa_circ_193547,RMVar_hsa_circ_62378 55468 RMVar_ID_55468 Human_SNP_ID_660601341 m1A Human chr19 - 18900435 18900435 18900435 GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCAGAGACGCTGGTCAACCTCATCGTCCTGTCCCA GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCCGAGACGCTGGTCAACCTCATCGTCCTGTCCCA T G COPE Ensembl:ENSG00000105669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18899957..18903468 26863196 MeRIP-seq:(Medium) rs1127821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53434,Human_RBP_ID_22476571,Human_RBP_ID_22762897 Human_Splice_Rec_1981398,Human_Splice_Rec_1981399,Human_Splice_Rec_1981414,Human_Splice_Rec_1981415,Human_Splice_Rec_1981420,Human_Splice_Rec_1981421,Human_Splice_Rec_1981440,Human_Splice_Rec_1981441,Human_Splice_Rec_1981454,Human_Splice_Rec_1981455,Human_Splice_Rec_1981470,Human_Splice_Rec_1981471,Human_Splice_Rec_1981482,Human_Splice_Rec_1981483 GWAS_ID_6631 RMVar_hsa_circ_193546,RMVar_hsa_circ_109918,RMVar_hsa_circ_86189,RMVar_hsa_circ_96801,RMVar_hsa_circ_193545,RMVar_hsa_circ_344320,RMVar_hsa_circ_193547,RMVar_hsa_circ_62378 55469 RMVar_ID_55469 Human_SNP_ID_660602911 m1A Human chr19 - 18904841 18904841 18904841 TGTCATCTGTCCCCGCCCCAGGAAGGAGCTGAAGAGAATGCAGGACCTGGACGAGGATGCCACCC TGTCATCTGTCCCCGCCCCAGGAAGGAGCTGAGGAGAATGCAGGACCTGGACGAGGATGCCACCC T C COPE Ensembl:ENSG00000105669 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18904716..18904903 26863196 MeRIP-seq:(Medium) rs946713207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239843,Human_RBP_ID_13397893,Human_RBP_ID_22533147,Human_RBP_ID_22662397 Human_Splice_Rec_1981394,Human_Splice_Rec_1981395,Human_Splice_Rec_1981412,Human_Splice_Rec_1981413,Human_Splice_Rec_1981436,Human_Splice_Rec_1981437,Human_Splice_Rec_1981450,Human_Splice_Rec_1981451,Human_Splice_Rec_1981466,Human_Splice_Rec_1981467 RMVar_hsa_circ_13254,RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_96801,RMVar_hsa_circ_344320,RMVar_hsa_circ_193547,RMVar_hsa_circ_331899,RMVar_hsa_circ_193548,RMVar_hsa_circ_113345,RMVar_hsa_circ_296065 55470 RMVar_ID_55470 Human_SNP_ID_660603277 m1A Human chr19 + 18905947 18905942 18905948 GCCCTGCCCGGACTCGACACCCTGGAGGCATCAACACTCAGGAACAAGGCCCTAGAGGAGGGCCA GCCCTGCCCGGACTCGACACCCTGGAGG______CACTCAGGAACAAGGCCCTAGAGGAGGGCCA GCATCAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18905945..18906110 26863196 MeRIP-seq:(Medium) rs1216682110 Functional Loss DEL dbSNP153 29..34 33 - - - 55471 RMVar_ID_55471 Human_SNP_ID_660603655 m1A Human chr19 - 18907083 18907083 18907083 CAGGGACAGCATCGTGGCCGAGCTGGACCGAGAGATGAGCAGGAGCGTGGACGTGACCAACACCA CAGGGACAGCATCGTGGCCGAGCTGGACCGAGGGATGAGCAGGAGCGTGGACGTGACCAACACCA T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18907033..18907149 26863196 MeRIP-seq:(Medium) rs769180190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516564,Human_RBP_ID_1556628,Human_RBP_ID_1881287,Human_RBP_ID_4511392,Human_RBP_ID_8839252,Human_RBP_ID_9293594,Human_RBP_ID_13397914,Human_RBP_ID_22448564 Human_Splice_Rec_1981390,Human_Splice_Rec_1981408,Human_Splice_Rec_1981430,Human_Splice_Rec_1981488,Human_Splice_Rec_1981508,Human_Splice_Rec_1981518 RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_296065,RMVar_hsa_circ_104727 55472 RMVar_ID_55472 Human_SNP_ID_660607165 m1A Human chr19 - 18919296 18919296 18919296 CCCGGCCTCCGGCGGCTCCGGGGAGGTAGACGAGCTGTTCGACGTAAAGAACGCCTTCTACATCG CCCGGCCTCCGGCGGCTCCGGGGAGGTAGACGGGCTGTTCGACGTAAAGAACGCCTTCTACATCG T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr19:18919201..18919397;chr19:18919273..18919356 26863410 MeRIP-seq:(Medium) rs555628077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1556634,Human_RBP_ID_4511404,Human_RBP_ID_5145719,Human_RBP_ID_5320292,Human_RBP_ID_5499132,Human_RBP_ID_9329939,Human_RBP_ID_22448566,Human_RBP_ID_23787136,Human_RBP_ID_26985735 Human_Splice_Rec_1981385,Human_Splice_Rec_1981403,Human_Splice_Rec_1981425,Human_Splice_Rec_1981459,Human_Splice_Rec_1981475,Human_Splice_Rec_1981489,Human_Splice_Rec_1981493 RMVar_hsa_circ_193546,RMVar_hsa_circ_86189 55473 RMVar_ID_55473 Human_SNP_ID_660607221 m1A Human chr19 + 18919340 18919340 18919340 CCGGAGCCGCCGGAGGCCGGGCCGGGGGCCGGAGGCGCCATTTCGCTGTCTTCTCACCAGCTCCT CCGGAGCCGCCGGAGGCCGGGCCGGGGGCCGGTGGCGCCATTTCGCTGTCTTCTCACCAGCTCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:18911361..18919400;chr19:18919201..18919375;chr19:18911361..18938530;chr19:18910889..18938530 26863196 MeRIP-seq:(Medium) rs1215818026 Functional Loss SNV dbSNP153 33..33 33 - - - 55474 RMVar_ID_55474 Human_SNP_ID_660607436 m1A Human chr19 - 18919775 18919775 18919775 CAAACCCAGCTGCCGACATTGTTCCACGAGCCACGATGACAGCCCGAGCTCCGCGAAGCCTGCCA CAAACCCAGCTGCCGACATTGTTCCACGAGCCTCGATGACAGCCCGAGCTCCGCGAAGCCTGCCA T A AC002985.1 Ensembl:ENSG00000268193 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18919701..18919875 26863196 MeRIP-seq:(Medium) rs993355167 Functional Loss SNV dbSNP153 33..33 33 - - - 55475 RMVar_ID_55475 Human_SNP_ID_660608061 m1A Human chr19 + 18921926 18921926 18921926 CCACGCCGGGGCGCCTGGCAGATCACCTGCGCAGCTCCAACACTTTTAGTATAAAGAAGATCCGC CCACGCCGGGGCGCCTGGCAGATCACCTGCGCGGCTCCAACACTTTTAGTATAAAGAAGATCCGC A G DDX49 Ensembl:ENSG00000105671 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18921875..18921976 32194978 MeRIP-seq:(Medium) rs775896736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17917376 Human_Splice_Rec_1981526,Human_Splice_Rec_1981527,Human_Splice_Rec_1981562,Human_Splice_Rec_1981563,Human_Splice_Rec_1981570,Human_Splice_Rec_1981571,Human_Splice_Rec_1981596,Human_Splice_Rec_1981597,Human_Splice_Rec_1981622,Human_Splice_Rec_1981623,Human_Splice_Rec_1981628,Human_Splice_Rec_1981629,Human_Splice_Rec_1981640,Human_Splice_Rec_1981641 Human_miRNA_ID_632936 RMVar_hsa_circ_26515,RMVar_hsa_circ_370573,RMVar_hsa_circ_101537,RMVar_hsa_circ_193552,RMVar_hsa_circ_193553 55476 RMVar_ID_55476 Human_SNP_ID_660608379 m1A Human chr19 + 18922660 18922660 18922660 CCAGCGCTACCTGCTGGTGCCTGAGAAGGTCAAGGACGCCTACCTGGTCCACCTGATCCAGCGCT CCAGCGCTACCTGCTGGTGCCTGAGAAGGTCAGGGACGCCTACCTGGTCCACCTGATCCAGCGCT A G DDX49 Ensembl:ENSG00000105671 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18922372..18922661 32194978 MeRIP-seq:(Medium) rs1303798273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18192976 Human_Splice_Rec_1981530,Human_Splice_Rec_1981531,Human_Splice_Rec_1981574,Human_Splice_Rec_1981575,Human_Splice_Rec_1981600,Human_Splice_Rec_1981601,Human_Splice_Rec_1981632,Human_Splice_Rec_1981633,Human_Splice_Rec_1981644,Human_Splice_Rec_1981645,Human_Splice_Rec_1981660,Human_Splice_Rec_1981661,Human_Splice_Rec_1981667,Human_Splice_Rec_1981677 RMVar_hsa_circ_26515,RMVar_hsa_circ_370573,RMVar_hsa_circ_2339,RMVar_hsa_circ_101537,RMVar_hsa_circ_193552,RMVar_hsa_circ_193553 55477 RMVar_ID_55477 Human_SNP_ID_660609100 m1A Human chr19 + 18924978 18924978 18924978 TACATCCACCGAGTCGGCCGGACGGCCCGTGCAGGTGAGCAGTGGAGGGGGAGGCCGAGCCTTGG TACATCCACCGAGTCGGCCGGACGGCCCGTGCGGGTGAGCAGTGGAGGGGGAGGCCGAGCCTTGG A G DDX49 Ensembl:ENSG00000105671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18924953..18925025 26863196 MeRIP-seq:(Medium) rs1366402109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1981536,Human_Splice_Rec_1981537,Human_Splice_Rec_1981580,Human_Splice_Rec_1981581,Human_Splice_Rec_1981607,Human_Splice_Rec_1981650,Human_Splice_Rec_1981651,Human_Splice_Rec_1981672,Human_Splice_Rec_1981673,Human_Splice_Rec_1981682,Human_Splice_Rec_1981683,Human_Splice_Rec_1981685 RMVar_hsa_circ_7447,RMVar_hsa_circ_26515,RMVar_hsa_circ_101537,RMVar_hsa_circ_193553,RMVar_hsa_circ_285889,RMVar_hsa_circ_311300,RMVar_hsa_circ_193554,RMVar_hsa_circ_344197,RMVar_hsa_circ_193555 55478 RMVar_ID_55478 Human_SNP_ID_660609964 m1A Human chr19 - 18927848 18927848 18927848 AGTTCCTGCCCGCCTCTGACACTCACGATCTCACACTCTCTTCGCACCACGTTGACCTGTGTGAG AGTTCCTGCCCGCCTCTGACACTCACGATCTCGCACTCTCTTCGCACCACGTTGACCTGTGTGAG T C AC002985.1 Ensembl:ENSG00000268193 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18927732..18927876 26863196 MeRIP-seq:(Medium) rs762854527 Functional Loss SNV dbSNP153 33..33 33 - - - 55479 RMVar_ID_55479 Human_SNP_ID_660610672 m1A Human chr19 + 18929576 18929576 18929576 GCGCCCGCTCCCGCTCTGCCCGTGCCTCCTCCAGGCTGCGCTCCATCGCCCGCAGCTGGTGCTCC GCGCCCGCTCCCGCTCTGCCCGTGCCTCCTCCTGGCTGCGCTCCATCGCCCGCAGCTGGTGCTCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:18929377..18934445;chr19:18929247..18938381 26863196 MeRIP-seq:(Medium) rs1339422162 Functional Loss SNV dbSNP153 33..33 33 - - - 55480 RMVar_ID_55480 Human_SNP_ID_660613376 m1A Human chr19 + 18938384 18938384 18938384 CCTGTGTCAGATGCTGTTCAGAGGCAAAGCCCAGGCCGTAGACTGTGTTGGCGCGACTGTCGGCC CCTGTGTCAGATGCTGTTCAGAGGCAAAGCCCGGGCCGTAGACTGTGTTGGCGCGACTGTCGGCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18938380..18938480 32194978 MeRIP-seq:(Medium) rs777911960 Functional Loss SNV dbSNP153 33..33 33 - - - 55481 RMVar_ID_55481 Human_SNP_ID_660614187 m1A Human chr19 - 18941094 18941094 18941094 CGGCAGCGCGGAGTCAGCGCCGCGGGGGCCGCACCCGACTCGCGCCTGGACACTCGCGGGGCGCC CGGCAGCGCGGAGTCAGCGCCGCGGGGGCCGCTCCCGACTCGCGCCTGGACACTCGCGGGGCGCC T A HOMER3 Ensembl:ENSG00000051128 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:18940908..18941114 26863196 MeRIP-seq:(Medium) rs1159527774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557380,Human_RBP_ID_9428153 Human_Splice_Rec_1981747,Human_Splice_Rec_1981765,Human_Splice_Rec_1981825 55482 RMVar_ID_55482 Human_SNP_ID_660614218 m1A Human chr19 + 18941180 18941168 18941180 CTCCCGGGCCCGCGCCCTCCGCGCCGCCCTCCACGCCGCCCGTGCCTTTGTCTGCGCCGCCGCCG CTCCCGGGCCCGCGCCCTCCG____________CGCCGCCCGTGCCTTTGTCTGCGCCGCCGCCG GCGCCGCCCTCCA G HOMER3-AS1 Ensembl:ENSG00000269019 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18940560..18946113 26863196 MeRIP-seq:(Medium) rs1247546587 Functional Loss DEL dbSNP153 22..33 33 - - - 55483 RMVar_ID_55483 Human_SNP_ID_660628604 m1A Human chr19 - 18994426 18994426 18994426 GGTGCTGACGGGCAGGAGCACAAAGAAGACACATTCGATGTGTTCCGACAGAGGATGATGCAGAT GGTGCTGACGGGCAGGAGCACAAAGAAGACACGTTCGATGTGTTCCGACAGAGGATGATGCAGAT T C SUGP2 Ensembl:ENSG00000064607 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18994401..18994425 32194978 MeRIP-seq:(Medium) rs1443942341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54858,Human_RBP_ID_1881305,Human_RBP_ID_4511496,Human_RBP_ID_9380824,Human_RBP_ID_13398297,Human_RBP_ID_25440734 Human_Splice_Rec_1981854,Human_Splice_Rec_1981855,Human_Splice_Rec_1981877,Human_Splice_Rec_1981904,Human_Splice_Rec_1981905,Human_Splice_Rec_1981926,Human_Splice_Rec_1981927,Human_Splice_Rec_1981946,Human_Splice_Rec_1981947,Human_Splice_Rec_1981971,Human_Splice_Rec_1981990,Human_Splice_Rec_1982008,Human_Splice_Rec_1982016,Human_Splice_Rec_1982017 RMVar_hsa_circ_47792,RMVar_hsa_circ_54514,RMVar_hsa_circ_73962,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_46519,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 55484 RMVar_ID_55484 Human_SNP_ID_660631243 m1A Human chr19 - 19004275 19004275 19004275 GGACGACCTGGCTGGAGCACCTGCCTTGTCACAGGCCTCCTCAGGTACCTGCTTCCCTCGGAAGA GGACGACCTGGCTGGAGCACCTGCCTTGTCACGGGCCTCCTCAGGTACCTGCTTCCCTCGGAAGA T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19004226..19004525 32194978 MeRIP-seq:(Medium) rs1426899610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52611,Human_RBP_ID_516620,Human_RBP_ID_769917,Human_RBP_ID_911042,Human_RBP_ID_3954765,Human_RBP_ID_5526931,Human_RBP_ID_8830617,Human_RBP_ID_18994672,Human_RBP_ID_22446610,Human_RBP_ID_26336060 RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_121444,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_337478,RMVar_hsa_circ_1434,RMVar_hsa_circ_347263,RMVar_hsa_circ_347485,RMVar_hsa_circ_193565,RMVar_hsa_circ_332124,RMVar_hsa_circ_312658,RMVar_hsa_circ_193566 55485 RMVar_ID_55485 Human_SNP_ID_660631321 m1A Human chr19 - 19004438 19004438 19004438 ACGAGCCCCCTCCGCGGGAGGCTGAGCTGGAGAGCCCAGAGGTGATGCCTGAGGAGGAGGACGAG ACGAGCCCCCTCCGCGGGAGGCTGAGCTGGAGCGCCCAGAGGTGATGCCTGAGGAGGAGGACGAG T G SUGP2 Ensembl:ENSG00000064607 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19004149..19004550 26863196 MeRIP-seq:(Medium) rs779469424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239092,Human_RBP_ID_912702,Human_RBP_ID_3956621,Human_RBP_ID_5526933,Human_RBP_ID_9085124,Human_RBP_ID_9380828,Human_RBP_ID_17934930,Human_RBP_ID_18470551,Human_RBP_ID_18994674,Human_RBP_ID_22449332,Human_RBP_ID_26336062 Human_Splice_Rec_1981871,Human_Splice_Rec_1981897 Human_miRNA_ID_2425616,Human_miRNA_ID_2435284,Human_miRNA_ID_2555188 RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_121444,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_337478,RMVar_hsa_circ_1434,RMVar_hsa_circ_347263,RMVar_hsa_circ_347485,RMVar_hsa_circ_193565,RMVar_hsa_circ_332124,RMVar_hsa_circ_312658,RMVar_hsa_circ_193566 55486 RMVar_ID_55486 Human_SNP_ID_660632938 m1A Human chr19 - 19009925 19009925 19009925 CCTCAGGACCCCAGCTTAGAAGCCTCAGGCCCATCCCCCAAGCCAGCAGGAGTGGACATCTCTGA CCTCAGGACCCCAGCTTAGAAGCCTCAGGCCCGTCCCCCAAGCCAGCAGGAGTGGACATCTCTGA T C SUGP2 Ensembl:ENSG00000064607 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:19009876..19010150 26863196 MeRIP-seq:(Medium) rs564916097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516634,Human_RBP_ID_909507,Human_RBP_ID_3954769,Human_RBP_ID_9382336,Human_RBP_ID_13398609,Human_RBP_ID_18192151,Human_RBP_ID_26985822,Human_RBP_ID_27465576 Human_Splice_Rec_1981867,Human_Splice_Rec_1981893,Human_Splice_Rec_1981917,Human_Splice_Rec_1981937,Human_Splice_Rec_1981959,Human_Splice_Rec_1981981,Human_Splice_Rec_1981999,Human_Splice_Rec_1982027 Human_miRNA_ID_2513210,Human_miRNA_ID_2653686,Human_miRNA_ID_2754884,Human_miRNA_ID_3056029 RMVar_hsa_circ_47792,RMVar_hsa_circ_121444,RMVar_hsa_circ_52054,RMVar_hsa_circ_1434,RMVar_hsa_circ_347485,RMVar_hsa_circ_332124,RMVar_hsa_circ_193566,RMVar_hsa_circ_334098,RMVar_hsa_circ_348184,RMVar_hsa_circ_34246,RMVar_hsa_circ_11075,RMVar_hsa_circ_57549,RMVar_hsa_circ_193568,RMVar_hsa_circ_41336 55487 RMVar_ID_55487 Human_SNP_ID_660632949 m1A Human chr19 + 19009958 19009958 19009958 GGGCCTGAGGCTTCTAAGCTGGGGTCCTGAGGAGAAGGTCCAACTGGGTCTGGCGGGCAGTCCTT GGGCCTGAGGCTTCTAAGCTGGGGTCCTGAGGGGAAGGTCCAACTGGGTCTGGCGGGCAGTCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19009855..19010269 26863196 MeRIP-seq:(Medium) rs778817411 Functional Loss SNV dbSNP153 33..33 33 - - - 55488 RMVar_ID_55488 Human_SNP_ID_660633032 m1A Human chr19 - 19010136 19010136 19010136 TCCGTGGCAGCGGCGGGGGCTCCTCCGTGCTCAAGGGCTCCGGGGCTGGAAGGCGAGGAGAGCGA TCCGTGGCAGCGGCGGGGGCTCCTCCGTGCTCGAGGGCTCCGGGGCTGGAAGGCGAGGAGAGCGA T C SUGP2 Ensembl:ENSG00000064607 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19010087..19010158 26863196 MeRIP-seq:(Medium) rs1239215328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912706,Human_RBP_ID_5526939,Human_RBP_ID_22231849,Human_RBP_ID_26336065 RMVar_hsa_circ_47792,RMVar_hsa_circ_121444,RMVar_hsa_circ_52054,RMVar_hsa_circ_1434,RMVar_hsa_circ_347485,RMVar_hsa_circ_332124,RMVar_hsa_circ_193566,RMVar_hsa_circ_334098,RMVar_hsa_circ_348184,RMVar_hsa_circ_34246,RMVar_hsa_circ_11075,RMVar_hsa_circ_57549,RMVar_hsa_circ_193568,RMVar_hsa_circ_41336 55489 RMVar_ID_55489 Human_SNP_ID_660639431 m1A Human chr19 - 19033476 19033476 19033476 TCGCGCGGCGGCGGCGGCGGGTGAGGAGCCTGAGGCGGCGGCGGGGGTGGCTCCGCGCGCGGTGG TCGCGCGGCGGCGGCGGCGGGTGAGGAGCCTGGGGCGGCGGCGGGGGTGGCTCCGCGCGCGGTGG T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19033373..19033500 26863196 MeRIP-seq:(Medium) rs967898155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824498,Human_RBP_ID_3954776,Human_RBP_ID_4558278,Human_RBP_ID_18420884 Human_Splice_Rec_1981885,Human_Splice_Rec_1981909,Human_Splice_Rec_1981929,Human_Splice_Rec_1981951,Human_Splice_Rec_1982035 55490 RMVar_ID_55490 Human_SNP_ID_660648022 m1A Human chr19 - 19064048 19064048 19064048 TTGGGCCCCCCCGGCGCCCCCCGCGCCCCCTCACCGGCCCGGACGCGTCGCCGCCGCCGCTACCT TTGGGCCCCCCCGGCGCCCCCCGCGCCCCCTCCCCGGCCCGGACGCGTCGCCGCCGCCGCTACCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19064017..19064115 26863196 MeRIP-seq:(Medium) rs908880601 Functional Loss SNV dbSNP153 33..33 33 - - - 55491 RMVar_ID_55491 Human_SNP_ID_660662293 m1A Human chr19 + 19120789 19120789 19120789 CATCTCACCCAGCGTCTTGAGCAGAAGTGTGCAGTTGAGGGTGAGGATGAGCGGCGTCAGGTACT CATCTCACCCAGCGTCTTGAGCAGAAGTGTGCGGTTGAGGGTGAGGATGAGCGGCGTCAGGTACT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:19120112..19120794 32194978 MeRIP-seq:(Medium) rs746727754 Functional Loss SNV dbSNP153 33..33 33 - - - 55492 RMVar_ID_55492 Human_SNP_ID_660665507 m1A Human chr19 + 19133200 19133200 19133200 GGCCCGAAGCTCCTCCTCAGACGGGTGCTTGTATCGGAACAAACTGAGAGCAAGGACGGGCAGTC GGCCCGAAGCTCCTCCTCAGACGGGTGCTTGTGTCGGAACAAACTGAGAGCAAGGACGGGCAGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19133151..19133225 32194978 MeRIP-seq:(Medium) rs752832735 Functional Loss SNV dbSNP153 33..33 33 - - - 55493 RMVar_ID_55493 Human_SNP_ID_660666713 m1A Human chr19 + 19138341 19138341 19138341 CTCAGAGCCTCCAATCCCCAAGAAGAAACCCCAATCCATTCCCTCAGTGTCTCCCTGGACCCCTT CTCAGAGCCTCCAATCCCCAAGAAGAAACCCCCATCCATTCCCTCAGTGTCTCCCTGGACCCCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19138331..19138425 26863196 MeRIP-seq:(Medium) rs946052008 Functional Loss SNV dbSNP153 33..33 33 - - - 55494 RMVar_ID_55494 Human_SNP_ID_660668541 m1A Human chr19 - 19145710 19145710 19145710 TGGGGACCCCACCTCCCTCCAGGCCTCTTCAGAGAAGACCCAACAGTGACGCCCCCCTCCGCGGT TGGGGACCCCACCTCCCTCCAGGCCTCTTCAGGGAAGACCCAACAGTGACGCCCCCCTCCGCGGT T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:19145701..19145830 26863196 MeRIP-seq:(Medium) rs1181618200 Functional Loss SNV dbSNP153 33..33 33 - - - 55495 RMVar_ID_55495 Human_SNP_ID_660674961 m1A Human chr19 - 19169962 19169962 19169962 GAAGTTGTGTGTCCAAGGGCTCTGCGTCTGAGATTTGGTGTGAGTTGGGGAGTTGGAGAGTTAGC GAAGTTGTGTGTCCAAGGGCTCTGCGTCTGAGGTTTGGTGTGAGTTGGGGAGTTGGAGAGTTAGC T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19169960..19170138 26863196 MeRIP-seq:(Medium) rs952927523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588113,Human_RBP_ID_8100541,Human_RBP_ID_17567627,Human_RBP_ID_23787399 RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 55496 RMVar_ID_55496 Human_SNP_ID_660674963 m1A Human chr19 + 19169974 19169974 19169974 ACTCCCCAACTCACACCAAATCTCAGACGCAGAGCCCTTGGACACACAACTTCCAGACCCACACC ACTCCCCAACTCACACCAAATCTCAGACGCAGTGCCCTTGGACACACAACTTCCAGACCCACACC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19169972..19170088 26863196 MeRIP-seq:(Medium) rs559250025 Functional Loss SNV dbSNP153 33..33 33 - - - 55497 RMVar_ID_55497 Human_SNP_ID_660675143 m1A Human chr19 - 19170583 19170583 19170583 AGTTGGGCCGAGTTAGGAAAAGGTTTAGAATTAGGGTTAGGGTCACAGTAGGGTCAGGGGTCGGC AGTTGGGCCGAGTTAGGAAAAGGTTTAGAATTTGGGTTAGGGTCACAGTAGGGTCAGGGGTCGGC T A MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19170579..19170670 26863196 MeRIP-seq:(Medium) rs1022389585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18724907 RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 55498 RMVar_ID_55498 Human_SNP_ID_660678576 m1A Human chr19 + 19182197 19182197 19182197 ACTGCCCCACATGGAACTCCGTCTGCCCCCGGATCGTCTCTGTCTGCATGTAACTCATGCCACCT ACTGCCCCACATGGAACTCCGTCTGCCCCCGGGTCGTCTCTGTCTGCATGTAACTCATGCCACCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19182191..19182359 26863196 MeRIP-seq:(Medium) rs1230780929 Functional Loss SNV dbSNP153 33..33 33 - - - 55499 RMVar_ID_55499 Human_SNP_ID_660678577 m1A Human chr19 + 19182197 19182197 19182197 ACTGCCCCACATGGAACTCCGTCTGCCCCCGGATCGTCTCTGTCTGCATGTAACTCATGCCACCT ACTGCCCCACATGGAACTCCGTCTGCCCCCGGTTCGTCTCTGTCTGCATGTAACTCATGCCACCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19182191..19182359 26863196 MeRIP-seq:(Medium) rs1230780929 Functional Loss SNV dbSNP153 33..33 33 - - - 55500 RMVar_ID_55500 Human_SNP_ID_660681399 m1A Human chr19 + 19192101 19192101 19192101 GGCCCGCACCACCTTTCTTCCCCTTGAGCTGCATCTCCGGCTCCTCCATAGCGACCGCGGCCGAG GGCCCGCACCACCTTTCTTCCCCTTGAGCTGCGTCTCCGGCTCCTCCATAGCGACCGCGGCCGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19191979..19192115 26863196 MeRIP-seq:(Medium) rs1258466785 Functional Loss SNV dbSNP153 33..33 33 - - - 55501 RMVar_ID_55501 Human_SNP_ID_660682020 m1A Human chr19 - 19193964 19193964 19193964 GGGGTCTGCTGGGTCTGGATGAGGTCTTCTGCAGGCTGGGTAAGCTCCATGGGGAAAGCTGGCGG GGGGTCTGCTGGGTCTGGATGAGGTCTTCTGCCGGCTGGGTAAGCTCCATGGGGAAAGCTGGCGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19192933..19194027 26863196 MeRIP-seq:(Medium) rs1439935606 Functional Loss SNV dbSNP153 33..33 33 - - - 55502 RMVar_ID_55502 Human_SNP_ID_660683289 m1A Human chr19 + 19198143 19198143 19198143 CCGACCCCCACATCCTGGCAAAAGAGCGAGAGAGCGCCCTGTCGCTGGCCAGCACAGGCGGCTAC CCGACCCCCACATCCTGGCAAAAGAGCGAGAGCGCGCCCTGTCGCTGGCCAGCACAGGCGGCTAC A C RFXANK Ensembl:ENSG00000064490 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19198101..19198225 26863196 MeRIP-seq:(Medium) rs751594870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18997325 Human_Splice_Rec_1982698,Human_Splice_Rec_1982699,Human_Splice_Rec_1982716,Human_Splice_Rec_1982717,Human_Splice_Rec_1982742,Human_Splice_Rec_1982743,Human_Splice_Rec_1982756,Human_Splice_Rec_1982757,Human_Splice_Rec_1982770,Human_Splice_Rec_1982771,Human_Splice_Rec_1982786,Human_Splice_Rec_1982787,Human_Splice_Rec_1982800,Human_Splice_Rec_1982801,Human_Splice_Rec_1982808 RMVar_hsa_circ_193600,RMVar_hsa_circ_31186,RMVar_hsa_circ_317586,RMVar_hsa_circ_295729 55503 RMVar_ID_55503 Human_SNP_ID_660684388 m1A Human chr19 + 19201621 19201621 19201621 GTGCCTCCACCCCACTCCCGATTCAAGCTCACAGCCCACCTTTTCCCTGCCCCATCTCAGTGCAA GTGCCTCCACCCCACTCCCGATTCAAGCTCACGGCCCACCTTTTCCCTGCCCCATCTCAGTGCAA A G RFXANK Ensembl:ENSG00000064490 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19201601..19201750 32194978 MeRIP-seq:(Medium) rs140834876 Functional Loss SNV dbSNP153 33..33 33 - - - 55504 RMVar_ID_55504 Human_SNP_ID_660705935 m1A Human chr19 - 19278773 19278773 19278773 TCTGAGCAGAATGGGCCGAGCAGCTGACAAAGATGGGCCGGGGCAAGCACTTCATCGGAGACTTC TCTGAGCAGAATGGGCCGAGCAGCTGACAAAGGTGGGCCGGGGCAAGCACTTCATCGGAGACTTC T C SUGP1 Ensembl:ENSG00000105705 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19278696..19278829 26863196 MeRIP-seq:(Medium) rs1409053891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1982996,Human_Splice_Rec_1982997,Human_Splice_Rec_1983022,Human_Splice_Rec_1983023,Human_Splice_Rec_1983036,Human_Splice_Rec_1983037,Human_Splice_Rec_1983062,Human_Splice_Rec_1983063,Human_Splice_Rec_1983086,Human_Splice_Rec_1983087,Human_Splice_Rec_1983096,Human_Splice_Rec_1983097 Human_miRNA_ID_770501,Human_miRNA_ID_775376,Human_miRNA_ID_780213,Human_miRNA_ID_785079,Human_miRNA_ID_789907,Human_miRNA_ID_1599587,Human_miRNA_ID_1609039,Human_miRNA_ID_1613955,Human_miRNA_ID_1621439,Human_miRNA_ID_1637554,Human_miRNA_ID_2316932,Human_miRNA_ID_2320086,Human_miRNA_ID_2323242,Human_miRNA_ID_2326419,Human_miRNA_ID_2520795,Human_miRNA_ID_2523962,Human_miRNA_ID_2823146,Human_miRNA_ID_2829278,Human_miRNA_ID_2832435,Human_miRNA_ID_2836559,Human_miRNA_ID_2841908,Human_miRNA_ID_2844036 RMVar_hsa_circ_90731,RMVar_hsa_circ_113202,RMVar_hsa_circ_193615,RMVar_hsa_circ_193617,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 55505 RMVar_ID_55505 Human_SNP_ID_660706067 m1A Human chr19 + 19279275 19279275 19279275 GCTGGTGCTCCCAGGTGCCCAGCTCGCTGTCCACCTCCTCATCACTGTCATAGCCGTGCTGGTGC GCTGGTGCTCCCAGGTGCCCAGCTCGCTGTCCGCCTCCTCATCACTGTCATAGCCGTGCTGGTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19279226..19279371 26863196 MeRIP-seq:(Medium) rs1568617106 Functional Loss SNV dbSNP153 33..33 33 - - - 55506 RMVar_ID_55506 Human_SNP_ID_660710877 m1A Human chr19 - 19297467 19297465 19297467 CAGGGCAGGAGGTCATGGTGGAGACCGTGACTATGACATGACCATATAGTGACCCTGGCCAACGT CAGGGCAGGAGGTCATGGTGGAGACCGTGACT__GACATGACCATATAGTGACCCTGGCCAACGT CAT C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19297465..19297559 26863196 MeRIP-seq:(Medium) rs911407646 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_193620,RMVar_hsa_circ_108551 55507 RMVar_ID_55507 Human_SNP_ID_660712482 m1A Human chr19 + 19303398 19303398 19303398 GCGACTTCTGTGCTTCCTTTCTTATCTCAGCCACCTTCTTCCTGTAGTAGAGGAATTCCCTGCTA GCGACTTCTGTGCTTCCTTTCTTATCTCAGCCGCCTTCTTCCTGTAGTAGAGGAATTCCCTGCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19303319..19303426 26863196 MeRIP-seq:(Medium) rs1285483889 Functional Loss SNV dbSNP153 33..33 33 - - - 55508 RMVar_ID_55508 Human_SNP_ID_660717729 m1A Human chr19 - 19320939 19320939 19320939 TGCGGAAGTGCTCAGCGAAGCCCAGAAGCGCCAGGTACCACGAGTCGGCCGCCTCGGCCTGCGCA TGCGGAAGTGCTCAGCGAAGCCCAGAAGCGCCGGGTACCACGAGTCGGCCGCCTCGGCCTGCGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19320888..19321074 26863196 MeRIP-seq:(Medium) rs1277822133 Functional Loss SNV dbSNP153 33..33 33 - - - 55509 RMVar_ID_55509 Human_SNP_ID_660717734 m1A Human chr19 - 19320946 19320946 19320946 CTGGAAGTGCGGAAGTGCTCAGCGAAGCCCAGAAGCGCCAGGTACCACGAGTCGGCCGCCTCGGC CTGGAAGTGCGGAAGTGCTCAGCGAAGCCCAGGAGCGCCAGGTACCACGAGTCGGCCGCCTCGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:19320851..19321000 26863410 MeRIP-seq:(Medium) rs1360912895 Functional Loss SNV dbSNP153 33..33 33 - - - 55510 RMVar_ID_55510 Human_SNP_ID_660717759 m1A Human chr19 - 19321029 19321029 19321029 GTGTACGGGCCTCGATGCGCTGCGGCGGCTTGAAGGGGAACACGGCCTGCAGGCAGTGCACGCAC GTGTACGGGCCTCGATGCGCTGCGGCGGCTTGTAGGGGAACACGGCCTGCAGGCAGTGCACGCAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19320930..19321081 32194978 MeRIP-seq:(Medium) rs749552628 Functional Loss SNV dbSNP153 33..33 33 - - - 55511 RMVar_ID_55511 Human_SNP_ID_660736066 m1A Human chr19 + 19385868 19385868 19385868 CAATTTCAGTGTGAGACTGAGCCGCGAGACTGAGCTGCGGCTCCGAGCGCTGCGCGGCGGCTCCT CAATTTCAGTGTGAGACTGAGCCGCGAGACTGGGCTGCGGCTCCGAGCGCTGCGCGGCGGCTCCT A G GATAD2A Ensembl:ENSG00000167491 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19385833..19385923 26863196 MeRIP-seq:(Medium) rs562558637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 55512 RMVar_ID_55512 Human_SNP_ID_660736080 m1A Human chr19 + 19385908 19385908 19385908 CTCCGAGCGCTGCGCGGCGGCTCCTCCCGCCCAGGGTCAGCGCCCCGGCGCGCGCACGCGCACCC CTCCGAGCGCTGCGCGGCGGCTCCTCCCGCCCTGGGTCAGCGCCCCGGCGCGCGCACGCGCACCC A T GATAD2A Ensembl:ENSG00000167491 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19385857..19385929 26863196 MeRIP-seq:(Medium) rs1363922022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 55513 RMVar_ID_55513 Human_SNP_ID_660749847 m1A Human chr19 - 19436077 19436077 19436077 GAAACACTGTGTTTCCAAGCAAGGTTTCTGGAACATACTGGCATTTCTAAAATGTCTCTAACCCC GAAACACTGTGTTTCCAAGCAAGGTTTCTGGACCATACTGGCATTTCTAAAATGTCTCTAACCCC T G lnc-TSSK6-4 RNACentral:URS0000D56CA3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19436075..19436188 26863196 MeRIP-seq:(Medium) rs139532966 Functional Loss SNV dbSNP153 33..33 33 - - - 55514 RMVar_ID_55514 Human_SNP_ID_660752888 m1A Human chr19 + 19447144 19447144 19447144 TGAATAAATAGCATGTCAAGTGGTGATGAGGCAGGAAAGGGGATAGAGACCCCCTGGGGGGCATG TGAATAAATAGCATGTCAAGTGGTGATGAGGCGGGAAAGGGGATAGAGACCCCCTGGGGGGCATG A G GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19447140..19447317 26863196 MeRIP-seq:(Medium) rs912032325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516 55515 RMVar_ID_55515 Human_SNP_ID_660757951 m1A Human chr19 + 19465413 19465413 19465413 ACGAGCGCTTGAACGGGACCCAACAGAGGACGATGTGGAGAGCAAGAAAATAAAAATGGAGAGAG ACGAGCGCTTGAACGGGACCCAACAGAGGACGCTGTGGAGAGCAAGAAAATAAAAATGGAGAGAG A C GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19464942..19465475 32194978 MeRIP-seq:(Medium) rs778441150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54369,Human_RBP_ID_1556792,Human_RBP_ID_1881389,Human_RBP_ID_6727958,Human_RBP_ID_9380837,Human_RBP_ID_13403836,Human_RBP_ID_18532303,Human_RBP_ID_26337733 Human_Splice_Rec_1983350,Human_Splice_Rec_1983352,Human_Splice_Rec_1983374,Human_Splice_Rec_1983386,Human_Splice_Rec_1983392,Human_Splice_Rec_1983400,Human_Splice_Rec_1983410,Human_Splice_Rec_1983432,Human_Splice_Rec_1983436 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516,RMVar_hsa_circ_316034,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_360303,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636 55516 RMVar_ID_55516 Human_SNP_ID_660757952 m1A Human chr19 + 19465413 19465413 19465413 ACGAGCGCTTGAACGGGACCCAACAGAGGACGATGTGGAGAGCAAGAAAATAAAAATGGAGAGAG ACGAGCGCTTGAACGGGACCCAACAGAGGACGGTGTGGAGAGCAAGAAAATAAAAATGGAGAGAG A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19464942..19465475 32194978 MeRIP-seq:(Medium) rs778441150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54369,Human_RBP_ID_1556792,Human_RBP_ID_1881389,Human_RBP_ID_6727958,Human_RBP_ID_9380837,Human_RBP_ID_13403836,Human_RBP_ID_18532303,Human_RBP_ID_26337733 Human_Splice_Rec_1983350,Human_Splice_Rec_1983352,Human_Splice_Rec_1983374,Human_Splice_Rec_1983386,Human_Splice_Rec_1983392,Human_Splice_Rec_1983400,Human_Splice_Rec_1983410,Human_Splice_Rec_1983432,Human_Splice_Rec_1983436 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516,RMVar_hsa_circ_316034,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_360303,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636 55517 RMVar_ID_55517 Human_SNP_ID_660757990 m1A Human chr19 - 19465527 19465527 19465527 CCATGGCCATGGCCGTGGCCTCTGTTGCCCTCAGCAATCCTTGGGTTGGACCTGCTCCCGGCTCA CCATGGCCATGGCCGTGGCCTCTGTTGCCCTCCGCAATCCTTGGGTTGGACCTGCTCCCGGCTCA T G lnc-TSSK6-4 RNACentral:URS0000D56CA3 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19465476..19472462 32194978 MeRIP-seq:(Medium) rs757972773 Functional Loss SNV dbSNP153 33..33 33 - - - 55518 RMVar_ID_55518 Human_SNP_ID_660758004 m1A Human chr19 + 19465556 19465556 19465556 TGCTGAGGGCAACAGAGGCCACGGCCATGGCCATGGGCAGAGGCGAAGGGCTGGTGGGCGATGGG TGCTGAGGGCAACAGAGGCCACGGCCATGGCCGTGGGCAGAGGCGAAGGGCTGGTGGGCGATGGG A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:19465376..19465638 26863196 MeRIP-seq:(Medium) rs201562141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54370,Human_RBP_ID_1013833,Human_RBP_ID_6727965,Human_RBP_ID_9380839,Human_RBP_ID_19089824,Human_RBP_ID_26336080 Human_Splice_Rec_1983353,Human_Splice_Rec_1983375,Human_Splice_Rec_1983387,Human_Splice_Rec_1983393,Human_Splice_Rec_1983401,Human_Splice_Rec_1983411,Human_Splice_Rec_1983433,Human_Splice_Rec_1983437,Human_Splice_Rec_1983457,Human_Splice_Rec_1983459 Human_miRNA_ID_2002236,Human_miRNA_ID_2003619,Human_miRNA_ID_2393840 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516,RMVar_hsa_circ_316034,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_360303,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636 55519 RMVar_ID_55519 Human_SNP_ID_660758022 m1A Human chr19 + 19465596 19465596 19465596 AGGCGAAGGGCTGGTGGGCGATGGGCCCGTGGACATGCGCACCTCACACAGGTGAGTGGGAGGAG AGGCGAAGGGCTGGTGGGCGATGGGCCCGTGGTCATGCGCACCTCACACAGGTGAGTGGGAGGAG A T GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:19465314..19465646;chr19:19465296..19472412;chr19:19465298..19465625 26863196 MeRIP-seq:(Medium) rs770664553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954786,Human_RBP_ID_5376279,Human_RBP_ID_6727967,Human_RBP_ID_8830662,Human_RBP_ID_9380839,Human_RBP_ID_19089824,Human_RBP_ID_26336080 Human_Splice_Rec_1983353,Human_Splice_Rec_1983375,Human_Splice_Rec_1983387,Human_Splice_Rec_1983393,Human_Splice_Rec_1983401,Human_Splice_Rec_1983411,Human_Splice_Rec_1983433,Human_Splice_Rec_1983437,Human_Splice_Rec_1983457,Human_Splice_Rec_1983459 Human_miRNA_ID_2007786 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516,RMVar_hsa_circ_316034,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_360303,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636 55520 RMVar_ID_55520 Human_SNP_ID_660761451 m1A Human chr19 + 19477565 19477565 19477565 CTGCAGCCCAGAAATCATGGTGCACCGGGTGCAGGGGTCAGAGTCTGAAGGTACACGGTGGTAGG CTGCAGCCCAGAAATCATGGTGCACCGGGTGCGGGGGTCAGAGTCTGAAGGTACACGGTGGTAGG A G GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19477557..19477738 26863196 MeRIP-seq:(Medium) rs1441580132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5193052,Human_RBP_ID_13404063 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636,RMVar_hsa_circ_193638 55521 RMVar_ID_55521 Human_SNP_ID_660765471 m1A Human chr19 + 19492631 19492631 19492631 CGAGAAAGGATGATCAAGCAGCTGAAGGAAGAATTGAGGTTAGAAGAAGCAAAACTCGTGTTGTT CGAGAAAGGATGATCAAGCAGCTGAAGGAAGAGTTGAGGTTAGAAGAAGCAAAACTCGTGTTGTT A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19492540..19492657 26863196 MeRIP-seq:(Medium) rs746647512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1556805,Human_RBP_ID_1881401,Human_RBP_ID_3564925,Human_RBP_ID_6728007,Human_RBP_ID_13404317,Human_RBP_ID_18994723,Human_RBP_ID_24545725,Human_RBP_ID_26336083 Human_Splice_Rec_1983356,Human_Splice_Rec_1983357,Human_Splice_Rec_1983390,Human_Splice_Rec_1983396,Human_Splice_Rec_1983404,Human_Splice_Rec_1983414,Human_Splice_Rec_1983415,Human_Splice_Rec_1983440,Human_Splice_Rec_1983441,Human_Splice_Rec_1983460,Human_Splice_Rec_1983461 RMVar_hsa_circ_60630,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_67955,RMVar_hsa_circ_193637,RMVar_hsa_circ_373234,RMVar_hsa_circ_127729,RMVar_hsa_circ_193636,RMVar_hsa_circ_193638,RMVar_hsa_circ_52887,RMVar_hsa_circ_310200,RMVar_hsa_circ_310628,RMVar_hsa_circ_271071,RMVar_hsa_circ_193641,RMVar_hsa_circ_193642,RMVar_hsa_circ_193640 55522 RMVar_ID_55522 Human_SNP_ID_660766486 m1A Human chr19 + 19495786 19495786 19495786 ACCTCTTCAGCTCGGATGCCCGGCAGTGTCATACCCCCGCCCCTGGTCCGAGGTGGGCAGCAGGC ACCTCTTCAGCTCGGATGCCCGGCAGTGTCATCCCCCCGCCCCTGGTCCGAGGTGGGCAGCAGGC A C GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19494373..19496075 26863196 MeRIP-seq:(Medium) rs775086481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911092,Human_RBP_ID_3956651,Human_RBP_ID_5376281,Human_RBP_ID_17272646,Human_RBP_ID_26815608,Human_RBP_ID_26986131 Human_Splice_Rec_1983360,Human_Splice_Rec_1983361,Human_Splice_Rec_1983418,Human_Splice_Rec_1983419,Human_Splice_Rec_1983444,Human_Splice_Rec_1983445,Human_Splice_Rec_1983462,Human_Splice_Rec_1983463 Human_miRNA_ID_2147382,Human_miRNA_ID_2147383,Human_miRNA_ID_2387402,Human_miRNA_ID_2387403,Human_miRNA_ID_2388875,Human_miRNA_ID_2388876,Human_miRNA_ID_2400022,Human_miRNA_ID_2400023,Human_miRNA_ID_2600190,Human_miRNA_ID_2600191,Human_miRNA_ID_2988808,Human_miRNA_ID_2988809,Human_miRNA_ID_3022509,Human_miRNA_ID_3022510,Human_miRNA_ID_3031083,Human_miRNA_ID_3031084 RMVar_hsa_circ_4246,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_193637,RMVar_hsa_circ_127729,RMVar_hsa_circ_193638,RMVar_hsa_circ_52887,RMVar_hsa_circ_310628,RMVar_hsa_circ_193642,RMVar_hsa_circ_317895,RMVar_hsa_circ_21263,RMVar_hsa_circ_290745,RMVar_hsa_circ_193643,RMVar_hsa_circ_52915,RMVar_hsa_circ_193644 55523 RMVar_ID_55523 Human_SNP_ID_660766521 m1A Human chr19 + 19495867 19495867 19495867 CCACAGGCGAGCTCACAGGTCGTCATGCCCCCACTCGTCAGGGGGGCTCAGGTAAGCAGGGCTGT CCACAGGCGAGCTCACAGGTCGTCATGCCCCCGCTCGTCAGGGGGGCTCAGGTAAGCAGGGCTGT A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19492692..19496060 32194978 MeRIP-seq:(Medium) rs1442730407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17272646,Human_RBP_ID_17382472 Human_Splice_Rec_1983361,Human_Splice_Rec_1983419,Human_Splice_Rec_1983445,Human_Splice_Rec_1983463 RMVar_hsa_circ_4246,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_193637,RMVar_hsa_circ_127729,RMVar_hsa_circ_193638,RMVar_hsa_circ_52887,RMVar_hsa_circ_310628,RMVar_hsa_circ_193642,RMVar_hsa_circ_317895,RMVar_hsa_circ_21263,RMVar_hsa_circ_290745,RMVar_hsa_circ_193643,RMVar_hsa_circ_52915,RMVar_hsa_circ_193644 55524 RMVar_ID_55524 Human_SNP_ID_660766524 m1A Human chr19 - 19495882 19495882 19495882 GTCTCCCCCATGTGCACAGCCCTGCTTACCTGAGCCCCCCTGACGAGTGGGGGCATGACGACCTG GTCTCCCCCATGTGCACAGCCCTGCTTACCTGGGCCCCCCTGACGAGTGGGGGCATGACGACCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19495719..19495921 26863196 MeRIP-seq:(Medium) rs1419868520 Functional Loss SNV dbSNP153 33..33 33 - - - 55525 RMVar_ID_55525 Human_SNP_ID_660767370 m1A Human chr19 - 19498529 19498529 19498529 GCGGCCGCCTGTCGGCTTGCTGGAGACTCGGCAGAGGTGACCACAGAGGCCACACTAGTGGGGGT GCGGCCGCCTGTCGGCTTGCTGGAGACTCGGCGGAGGTGACCACAGAGGCCACACTAGTGGGGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19498482..19498625 26863196 MeRIP-seq:(Medium) rs769064807 Functional Loss SNV dbSNP153 33..33 33 - - - 55526 RMVar_ID_55526 Human_SNP_ID_660767371 m1A Human chr19 - 19498529 19498529 19498529 GCGGCCGCCTGTCGGCTTGCTGGAGACTCGGCAGAGGTGACCACAGAGGCCACACTAGTGGGGGT GCGGCCGCCTGTCGGCTTGCTGGAGACTCGGCCGAGGTGACCACAGAGGCCACACTAGTGGGGGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19498482..19498625 26863196 MeRIP-seq:(Medium) rs769064807 Functional Loss SNV dbSNP153 33..33 33 - - - 55527 RMVar_ID_55527 Human_SNP_ID_660767394 m1A Human chr19 + 19498564 19498564 19498564 CGAGTCTCCAGCAAGCCGACAGGCGGCCGCCAAGCTGGCGCTGCGCAAACAGCTGGAGAAGACGC CGAGTCTCCAGCAAGCCGACAGGCGGCCGCCAGGCTGGCGCTGCGCAAACAGCTGGAGAAGACGC A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:19498551..19498575 26863196 MeRIP-seq:(Medium) rs780682840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4246,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_52887,RMVar_hsa_circ_21263,RMVar_hsa_circ_26247,RMVar_hsa_circ_193645,RMVar_hsa_circ_332678 55528 RMVar_ID_55528 Human_SNP_ID_660768187 m1A Human chr19 + 19501245 19501245 19501245 AGCGGCGCCATCATGTGTGAGAACTGCATGACAACCAACCAGAAGAAGGCGCTCAAGGTGGAGCA AGCGGCGCCATCATGTGTGAGAACTGCATGACGACCAACCAGAAGAAGGCGCTCAAGGTGGAGCA A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19501195..19501342 26863196 MeRIP-seq:(Medium) rs763325116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1556815,Human_RBP_ID_5585501,Human_RBP_ID_6728023,Human_RBP_ID_9380840,Human_RBP_ID_13404413 Human_miRNA_ID_2443156 RMVar_hsa_circ_4246,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_52887,RMVar_hsa_circ_21263,RMVar_hsa_circ_193645,RMVar_hsa_circ_332678,RMVar_hsa_circ_14701 55529 RMVar_ID_55529 Human_SNP_ID_660768690 m1A Human chr19 + 19502511 19502511 19502511 GCAAGGGCAGCGCCACCTCCAACTGGAAGAAGACGCCCCTCAGCACAGGTGGGTGACCTCCACAG GCAAGGGCAGCGCCACCTCCAACTGGAAGAAGGCGCCCCTCAGCACAGGTGGGTGACCTCCACAG A G GATAD2A Ensembl:ENSG00000167491 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:19502401..19502632 26863196 MeRIP-seq:(Medium) rs142116086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516833,Human_RBP_ID_9294368 Human_Splice_Rec_1983371,Human_Splice_Rec_1983383,Human_Splice_Rec_1983429,Human_Splice_Rec_1983455,Human_Splice_Rec_1983471 Human_miRNA_ID_2391212,Human_miRNA_ID_2592457 RMVar_hsa_circ_4246,RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_52887,RMVar_hsa_circ_8588,RMVar_hsa_circ_21263,RMVar_hsa_circ_193645,RMVar_hsa_circ_332678,RMVar_hsa_circ_14701 55530 RMVar_ID_55530 Human_SNP_ID_660769825 m1A Human chr19 + 19506195 19506195 19506195 CGAGGCAGCCCTCGCTCCAGCTGAACGCCTCCATTGCTGCTTGTTCTGGAGACCCCCGCCCCCGC CGAGGCAGCCCTCGCTCCAGCTGAACGCCTCCGTTGCTGCTTGTTCTGGAGACCCCCGCCCCCGC A G GATAD2A Ensembl:ENSG00000167491 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19506086..19506291 26863196 MeRIP-seq:(Medium) rs909007787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516854,Human_RBP_ID_4512290,Human_RBP_ID_6728080,Human_RBP_ID_8830692,Human_RBP_ID_13404498,Human_RBP_ID_22371150,Human_RBP_ID_26472351 Human_miRNA_ID_2102425,Human_miRNA_ID_2108380,Human_miRNA_ID_2114318,Human_miRNA_ID_2166864,Human_miRNA_ID_2598122,Human_miRNA_ID_2741028,Human_miRNA_ID_3041616 RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 55531 RMVar_ID_55531 Human_SNP_ID_660769841 m1A Human chr19 + 19506237 19506237 19506237 GTTCTGGAGACCCCCGCCCCCGCACCTTCCAGACTTAGCAGAAGAACAAACTGAAGAACAGACCC GTTCTGGAGACCCCCGCCCCCGCACCTTCCAGGCTTAGCAGAAGAACAAACTGAAGAACAGACCC A G GATAD2A Ensembl:ENSG00000167491 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19506051..19506350 26863196 MeRIP-seq:(Medium) rs1336723883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516854,Human_RBP_ID_1881412,Human_RBP_ID_5585502,Human_RBP_ID_13404498,Human_RBP_ID_18302139,Human_RBP_ID_22070066,Human_RBP_ID_26472352 Human_miRNA_ID_1547240 RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 55532 RMVar_ID_55532 Human_SNP_ID_660773102 m1A Human chr19 + 19516261 19516261 19516261 TACTGCGAGTATGGCGGCGTCAAAGGTGAAGCAGGACATGCCTCCGCCGGGGGGCTATGGGCCCA TACTGCGAGTATGGCGGCGTCAAAGGTGAAGCCGGACATGCCTCCGCCGGGGGGCTATGGGCCCA A C NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:19516246..19516375 26863196 MeRIP-seq:(Medium) rs1003592932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138703,Human_RBP_ID_240752,Human_RBP_ID_516914,Human_RBP_ID_772242,Human_RBP_ID_826520,Human_RBP_ID_4512356,Human_RBP_ID_5116829,Human_RBP_ID_17656050,Human_RBP_ID_22446620,Human_RBP_ID_26336088,Human_RBP_ID_27815333 Human_Splice_Rec_1983479,Human_Splice_Rec_1983487,Human_Splice_Rec_1983495,Human_Splice_Rec_1983503,Human_Splice_Rec_1983505,Human_Splice_Rec_1983511,Human_Splice_Rec_1983515,Human_Splice_Rec_1983523,Human_Splice_Rec_1983535 Human_miRNA_ID_2476706,Human_miRNA_ID_2962489 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 55533 RMVar_ID_55533 Human_SNP_ID_660773103 m1A Human chr19 + 19516261 19516261 19516261 TACTGCGAGTATGGCGGCGTCAAAGGTGAAGCAGGACATGCCTCCGCCGGGGGGCTATGGGCCCA TACTGCGAGTATGGCGGCGTCAAAGGTGAAGCGGGACATGCCTCCGCCGGGGGGCTATGGGCCCA A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:19516246..19516375 26863196 MeRIP-seq:(Medium) rs1003592932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138703,Human_RBP_ID_240752,Human_RBP_ID_516914,Human_RBP_ID_772242,Human_RBP_ID_826520,Human_RBP_ID_4512356,Human_RBP_ID_5116829,Human_RBP_ID_17656050,Human_RBP_ID_22446620,Human_RBP_ID_26336088,Human_RBP_ID_27815333 Human_Splice_Rec_1983479,Human_Splice_Rec_1983487,Human_Splice_Rec_1983495,Human_Splice_Rec_1983503,Human_Splice_Rec_1983505,Human_Splice_Rec_1983511,Human_Splice_Rec_1983515,Human_Splice_Rec_1983523,Human_Splice_Rec_1983535 Human_miRNA_ID_2476706,Human_miRNA_ID_2962489 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 55534 RMVar_ID_55534 Human_SNP_ID_660773151 m1A Human chr19 + 19516303 19516303 19516303 TCCGCCGGGGGGCTATGGGCCCATCGACTACAAACGGAACTTGCCGCGTCGAGGACTGTCGGGTC TCCGCCGGGGGGCTATGGGCCCATCGACTACAGACGGAACTTGCCGCGTCGAGGACTGTCGGGTC A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs775019067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138703,Human_RBP_ID_240752,Human_RBP_ID_1556827,Human_RBP_ID_3564946,Human_RBP_ID_4512358,Human_RBP_ID_5116830,Human_RBP_ID_9085183,Human_RBP_ID_9328860,Human_RBP_ID_9382349,Human_RBP_ID_13404629,Human_RBP_ID_22447620,Human_RBP_ID_23114768,Human_RBP_ID_23787743,Human_RBP_ID_26336088,Human_RBP_ID_27815333 Human_Splice_Rec_1983479,Human_Splice_Rec_1983487,Human_Splice_Rec_1983495,Human_Splice_Rec_1983503,Human_Splice_Rec_1983505,Human_Splice_Rec_1983511,Human_Splice_Rec_1983515,Human_Splice_Rec_1983523,Human_Splice_Rec_1983535 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 55535 RMVar_ID_55535 Human_SNP_ID_660773168 m1A Human chr19 - 19516329 19516329 19516329 CTGAGACCCCGGCGCAGAGTGATACTGACCCGACAGTCCTCGACGCGGCAAGTTCCGTTTGTAGT CTGAGACCCCGGCGCAGAGTGATACTGACCCGCCAGTCCTCGACGCGGCAAGTTCCGTTTGTAGT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:19516226..19526275 26863410 MeRIP-seq:(Medium) rs991529032 Functional Loss SNV dbSNP153 33..33 33 - - - 55536 RMVar_ID_55536 Human_SNP_ID_660776173 m1A Human chr19 - 19527300 19527300 19527300 TAACAGTGGCAACAGCGCGATGCGAGCCTCGAAGTCCTCGATTTGTAGGCGCCTGTGAAAGCCCG TAACAGTGGCAACAGCGCGATGCGAGCCTCGATGTCCTCGATTTGTAGGCGCCTGTGAAAGCCCG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19527276..19527300 26863196 MeRIP-seq:(Medium) rs769863677 Functional Loss SNV dbSNP153 33..33 33 - - - 55537 RMVar_ID_55537 Human_SNP_ID_660776267 m1A Human chr19 + 19527518 19527518 19527518 GCGTGGAGACTTAGTGGAGACCCAAGGGGGCGAACCGGAAGGCTTCCTGGAGGAGGAGGCAGCAC GCGTGGAGACTTAGTGGAGACCCAAGGGGGCGGACCGGAAGGCTTCCTGGAGGAGGAGGCAGCAC A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19527515..19527614 26863196 MeRIP-seq:(Medium) rs1455675013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26337742 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647,RMVar_hsa_circ_290843,RMVar_hsa_circ_361624,RMVar_hsa_circ_193648 55538 RMVar_ID_55538 Human_SNP_ID_660776551 m1A Human chr19 - 19528138 19528138 19528138 CAGTGGGGAGGGGCAGGGATCCAGGTGGCCGGAGGGCACAGGGCCTACGTGTACCACATGAAGCC CAGTGGGGAGGGGCAGGGATCCAGGTGGCCGGGGGGCACAGGGCCTACGTGTACCACATGAAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19528001..19529426 32194978 MeRIP-seq:(Medium) rs1163693600 Functional Loss SNV dbSNP153 33..33 33 - - - 55539 RMVar_ID_55539 Human_SNP_ID_660777251 m1A Human chr19 - 19530056 19530027 19530057 CTCTCAGTCCTACCTGCTTCTCTCCACCTCACACCTCTGCCCACCAGACCACCACGGGGGATCAC CTCTCAGTCCTACCTGCTTCTCTCCACCTCA______________________________TCAC ATCCCCCGTGGTGGTCTGGTGGGCAGAGGTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19530006..19530110 26863196 MeRIP-seq:(Medium) rs1343947884 Functional Loss DEL dbSNP153 32..61 33 - - - 55540 RMVar_ID_55540 Human_SNP_ID_660777260 m1A Human chr19 - 19530056 19530056 19530056 CTCTCAGTCCTACCTGCTTCTCTCCACCTCACACCTCTGCCCACCAGACCACCACGGGGGATCAC CTCTCAGTCCTACCTGCTTCTCTCCACCTCACTCCTCTGCCCACCAGACCACCACGGGGGATCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19530006..19530110 26863196 MeRIP-seq:(Medium) rs565779167 Functional Loss SNV dbSNP153 33..33 33 - - - 55541 RMVar_ID_55541 Human_SNP_ID_660779032 m1A Human chr19 - 19535635 19535635 19535635 CCAGGCTCACGAGGGGGATGGACAGCAGCTTGAGCGTGGCCAGCGCGCGGGTGCAGGGGCCCCCG CCAGGCTCACGAGGGGGATGGACAGCAGCTTGGGCGTGGCCAGCGCGCGGGTGCAGGGGCCCCCG T C lnc-TSSK6-3 RNACentral:URS00008C4022 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:19535584..19535711 26863196 MeRIP-seq:(Medium) rs1266829083 Functional Loss SNV dbSNP153 33..33 33 - - - 55542 RMVar_ID_55542 Human_SNP_ID_660779419 m1A Human chr19 + 19536940 19536940 19536940 TGCAGTGAGCCGAGATTGCACCATTGCACTCCAGCCTGGGTGACTGAAGACAGAGGCTGGGTCAG TGCAGTGAGCCGAGATTGCACCATTGCACTCCGGCCTGGGTGACTGAAGACAGAGGCTGGGTCAG A G YJEFN3 Ensembl:ENSG00000250067 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19536935..19537115 26863196 MeRIP-seq:(Medium) rs1354909457 Functional Loss SNV dbSNP153 33..33 33 - - - 55543 RMVar_ID_55543 Human_SNP_ID_660779439 m1A Human chr19 + 19537004 19537004 19537004 GATGGAGGAGGGCGATTGAATAGTAGGATAGGAGCAGAAGCAGAAAGTCTGAGTGCAGAAGCTCT GATGGAGGAGGGCGATTGAATAGTAGGATAGGGGCAGAAGCAGAAAGTCTGAGTGCAGAAGCTCT A G YJEFN3 Ensembl:ENSG00000250067 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19536953..19537077 26863196 MeRIP-seq:(Medium) rs537251557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13405143 55544 RMVar_ID_55544 Human_SNP_ID_660790823 m1A Human chr19 - 19575486 19575486 19575486 GACTACAGAGAGGACAGCCATTGTCTGTTTTGAGCCAGGAGAGATTAGGAGGAGAGGGGAGGGTT GACTACAGAGAGGACAGCCATTGTCTGTTTTGGGCCAGGAGAGATTAGGAGGAGAGGGGAGGGTT T C PBX4 Ensembl:ENSG00000105717 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19575484..19575638 26863196 MeRIP-seq:(Medium) rs1454680472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294980,RMVar_hsa_circ_193656,RMVar_hsa_circ_25911 55545 RMVar_ID_55545 Human_SNP_ID_660800982 m1A Human chr19 - 19618155 19618155 19618155 TGCGGCTGGAAGTTTTTTTGTTGTTGTTTGACACGGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA TGCGGCTGGAAGTTTTTTTGTTGTTGTTTGACGCGGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA T C PBX4 Ensembl:ENSG00000105717 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19618154..19618514 26863196 MeRIP-seq:(Medium) rs541557315 Functional Loss SNV dbSNP153 33..33 33 - - - 55546 RMVar_ID_55546 Human_SNP_ID_660804350 m1A Human chr19 + 19630023 19630023 19630023 TGGACGTCCGGGCAGCAGGTGGCCCTGGGCACAGCCTCGCTGTCCAATTTCGAGAGTAGCCGGGC TGGACGTCCGGGCAGCAGGTGGCCCTGGGCACGGCCTCGCTGTCCAATTTCGAGAGTAGCCGGGC A G lnc-ZNF101-1 RNACentral:URS0000D5E368 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19629974..19630124 32194978 MeRIP-seq:(Medium) rs1445105584 Functional Loss SNV dbSNP153 33..33 33 - - - 55547 RMVar_ID_55547 Human_SNP_ID_660805807 m1A Human chr19 - 19635069 19635069 19635069 GGGACTTCCCGGAGGAGGTACCCTTTGTGGTCACGAAGTGCACGGCTGAGATAGAACACCGTGCC GGGACTTCCCGGAGGAGGTACCCTTTGTGGTCCCGAAGTGCACGGCTGAGATAGAACACCGTGCC T G GMIP Ensembl:ENSG00000089639 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19634923..19635569 32194978 MeRIP-seq:(Medium) rs767951734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585508 Human_Splice_Rec_1983715,Human_Splice_Rec_1983753,Human_Splice_Rec_1983765 RMVar_hsa_circ_103925,RMVar_hsa_circ_115029,RMVar_hsa_circ_193660,RMVar_hsa_circ_43541,RMVar_hsa_circ_193661,RMVar_hsa_circ_267780 55548 RMVar_ID_55548 Human_SNP_ID_660808519 m1A Human chr19 - 19643529 19643529 19643529 CGGTCCCTGCAGAGCGATCCCCGGGCCCAGATATGGACGCAGCAGAGCCGGGTAGGGGGTCGGGG CGGTCCCTGCAGAGCGATCCCCGGGCCCAGATGTGGACGCAGCAGAGCCGGGTAGGGGGTCGGGG T C GMIP Ensembl:ENSG00000089639 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19643527..19643618 26863196 MeRIP-seq:(Medium) rs1436539664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558294 Human_Splice_Rec_1983685,Human_Splice_Rec_1983725,Human_Splice_Rec_1983791,Human_Splice_Rec_1983807,Human_Splice_Rec_1983821 55549 RMVar_ID_55549 Human_SNP_ID_660809748 m1A Human chr19 - 19647119 19647119 19647119 TCCTCTTCATCTCCCGTTCCAAGGTGGGCCCCAGAGGTGCTGGAAGGCCAGGGATGCATGGGCCT TCCTCTTCATCTCCCGTTCCAAGGTGGGCCCCCGAGGTGCTGGAAGGCCAGGGATGCATGGGCCT T G ATP13A1 Ensembl:ENSG00000105726 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19647118..19647249 26863196 MeRIP-seq:(Medium) rs1233385203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19089834,Human_RBP_ID_26785563 RMVar_hsa_circ_117158,RMVar_hsa_circ_320198,RMVar_hsa_circ_119863,RMVar_hsa_circ_115848,RMVar_hsa_circ_193668,RMVar_hsa_circ_193670,RMVar_hsa_circ_193672,RMVar_hsa_circ_76597,RMVar_hsa_circ_193671,RMVar_hsa_circ_193669,RMVar_hsa_circ_193675,RMVar_hsa_circ_101579 55550 RMVar_ID_55550 Human_SNP_ID_660810745 m1A Human chr19 - 19649785 19649785 19649785 AGGCCACCGACCCCCAGCAGCTGCTCCGCCTCATCCCCCATGTGCAGGTGTTCGCCCGTGTGGCT AGGCCACCGACCCCCAGCAGCTGCTCCGCCTCGTCCCCCATGTGCAGGTGTTCGCCCGTGTGGCT T C ATP13A1 Ensembl:ENSG00000105726 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19649532..19649902 26863196 MeRIP-seq:(Medium) rs768787610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954802,Human_RBP_ID_17917606 Human_Splice_Rec_1983869,Human_Splice_Rec_1983919,Human_Splice_Rec_1983937,Human_Splice_Rec_1983963,Human_Splice_Rec_1983997 RMVar_hsa_circ_117158,RMVar_hsa_circ_119863,RMVar_hsa_circ_115848,RMVar_hsa_circ_193668,RMVar_hsa_circ_193670,RMVar_hsa_circ_193669,RMVar_hsa_circ_58241,RMVar_hsa_circ_193675,RMVar_hsa_circ_101579,RMVar_hsa_circ_265481,RMVar_hsa_circ_80617,RMVar_hsa_circ_193677,RMVar_hsa_circ_23564,RMVar_hsa_circ_312385,RMVar_hsa_circ_59774,RMVar_hsa_circ_193679 55551 RMVar_ID_55551 Human_SNP_ID_660810771 m1A Human chr19 + 19649830 19649830 19649830 CTGCTGGGGGTCGGTGGCCTGCAGGTGGGCCAAGCCGTCGCCTGTGAGGCACAGTGCGTACTCCA CTGCTGGGGGTCGGTGGCCTGCAGGTGGGCCAGGCCGTCGCCTGTGAGGCACAGTGCGTACTCCA A G lnc-ZNF101-1 RNACentral:URS0000D5E368 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:19649726..19649921 26863196 MeRIP-seq:(Medium) rs955019781 Functional Loss SNV dbSNP153 33..33 33 - - - 55552 RMVar_ID_55552 Human_SNP_ID_660810816 m1A Human chr19 + 19649920 19649920 19649920 GGCCAGGGGCAGCACGATGCTGCCGTCAATGGAGCGCCACTCGCACTGCCGGCCTGCGGGCAGCA GGCCAGGGGCAGCACGATGCTGCCGTCAATGGCGCGCCACTCGCACTGCCGGCCTGCGGGCAGCA A C lnc-ZNF101-1 RNACentral:URS0000D5E368 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19649873..19649973 32194978 MeRIP-seq:(Medium) rs1233733560 Functional Loss SNV dbSNP153 33..33 33 - - - 55553 RMVar_ID_55553 Human_SNP_ID_660810962 m1A Human chr19 - 19650319 19650319 19650319 AGAAAACAGGATTTCAGAGAGGCCACGGGCGCAGGGATAAATGAGGTGAGGGCCTGGTGTGGGGT AGAAAACAGGATTTCAGAGAGGCCACGGGCGCCGGGATAAATGAGGTGAGGGCCTGGTGTGGGGT T G ATP13A1 Ensembl:ENSG00000105726 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19650317..19650599 26863196 MeRIP-seq:(Medium) rs907891126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6728259,Human_RBP_ID_13405618 RMVar_hsa_circ_117158,RMVar_hsa_circ_119863,RMVar_hsa_circ_115848,RMVar_hsa_circ_193668,RMVar_hsa_circ_193670,RMVar_hsa_circ_193669,RMVar_hsa_circ_58241,RMVar_hsa_circ_193675,RMVar_hsa_circ_101579,RMVar_hsa_circ_265481,RMVar_hsa_circ_80617,RMVar_hsa_circ_193677,RMVar_hsa_circ_23564,RMVar_hsa_circ_59774 55554 RMVar_ID_55554 Human_SNP_ID_660815346 m1A Human chr19 - 19663593 19663578 19663593 GGCCCGGCCTTGCGGGGTCCGGCCTGACGGGCAGCCCAAGCCCGGGCCGCAGCCGCGCGCGCTCC GGCCCGGCCTTGCGGGGTCCGGCCTGACGGGC_______________CGCAGCCGCGCGCGCTCC GGCCCGGGCTTGGGCT G ATP13A1 Ensembl:ENSG00000105726 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19663545..19663625 26863196 MeRIP-seq:(Medium) rs1315822470 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_241445,Human_RBP_ID_304175,Human_RBP_ID_4557388,Human_RBP_ID_22447637 55555 RMVar_ID_55555 Human_SNP_ID_661221370 m1A Human chr19 + 21142136 21142136 21142136 GCCCAACATCTGTGGCCCTGTGACCTGCAGGTATTGGGAGACCCACAGCTAAGACACCGGGACCC GCCCAACATCTGTGGCCCTGTGACCTGCAGGTGTTGGGAGACCCACAGCTAAGACACCGGGACCC A G ZNF431 Ensembl:ENSG00000196705 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:21142085..21142161 26863196 MeRIP-seq:(Medium) rs1329714369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558300,Human_RBP_ID_18420894,Human_RBP_ID_18725502,Human_RBP_ID_26336105 Human_Splice_Rec_1984765,Human_Splice_Rec_1984775,Human_Splice_Rec_1984785,Human_Splice_Rec_1984789,Human_Splice_Rec_1984797 RMVar_hsa_circ_88485,RMVar_hsa_circ_193718 55556 RMVar_ID_55556 Human_SNP_ID_661257586 m1A Human chr19 - 21286821 21286820 21286822 AGGAAAGGAAGAAAGGAGAGAGAAAGAAAGAGAAGCAAGAAAAGGAGAGAAGGAAAGGAAGAAAG AGGAAAGGAAGAAAGGAGAGAGAAAGAAAGA__AGCAAGAAAAGGAGAGAAGGAAAGGAAGAAAG TTC T lnc-ZNF708-12 RNACentral:URS0000D57990 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:21286771..21286848 26863196 MeRIP-seq:(Medium) rs1196341161 Functional Loss DEL dbSNP153 32..33 33 - - - 55557 RMVar_ID_55557 Human_SNP_ID_661257594 m1A Human chr19 - 21286840 21286840 21286840 GAAGAAAGAAAAGGAGAGAAGGAAAGGAAGAAAGGAGAGAGAAAGAAAGAGAAGCAAGAAAAGGA GAAGAAAGAAAAGGAGAGAAGGAAAGGAAGAAGGGAGAGAGAAAGAAAGAGAAGCAAGAAAAGGA T C lnc-ZNF708-12 RNACentral:URS0000D57990 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:21286793..21286938 26863196 MeRIP-seq:(Medium) rs1235396185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2560814 55558 RMVar_ID_55558 Human_SNP_ID_661276546 m1A Human chr19 - 21359072 21359072 21359072 GGATTCCCAATACCTGCAGGTCACAGGACCAGAGGCTGGGCCTCTAGGAGCAGAGGACACAGAGC GGATTCCCAATACCTGCAGGTCACAGGACCAGCGGCTGGGCCTCTAGGAGCAGAGGACACAGAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:21359025..21359092 26863196 MeRIP-seq:(Medium) rs1451118785 Functional Loss SNV dbSNP153 33..33 33 - - - 55559 RMVar_ID_55559 Human_SNP_ID_661809199 m1A Human chr19 - 23345574 23345574 23345574 GGGTCGGGAAGAGGAAGGCAATCTGGGTGGTGAGAACAGAGGAGGAGGATTTGAACACATGAGCA GGGTCGGGAAGAGGAAGGCAATCTGGGTGGTGCGAACAGAGGAGGAGGATTTGAACACATGAGCA T G ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:23345524..23345906 26863196 MeRIP-seq:(Medium) rs1490897495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_202708,Human_RBP_ID_9425252 RMVar_hsa_circ_193757,RMVar_hsa_circ_193758,RMVar_hsa_circ_193760,RMVar_hsa_circ_193759 55560 RMVar_ID_55560 Human_SNP_ID_662000378 m1A Human chr19 - 24001321 24001321 24001321 GTCCCAGGTGCAGATCTTGGTGGTAGTAGCAAATATTCAAATGAGAACTTTGAAGGCCGAAGTGG GTCCCAGGTGCAGATCTTGGTGGTAGTAGCAAGTATTCAAATGAGAACTTTGAAGGCCGAAGTGG T C RF02543-023 RNACentral:URS00009843EB rRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr19:24001233..24001406;chr19:24001219..24001412;chr19:24001263..24001382 26863196 MeRIP-seq:(Medium) rs1568405978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270072,Human_RBP_ID_279375,Human_RBP_ID_518086,Human_RBP_ID_1014135,Human_RBP_ID_1094780,Human_RBP_ID_1132841,Human_RBP_ID_1188168,Human_RBP_ID_1239750,Human_RBP_ID_1292815,Human_RBP_ID_1372380,Human_RBP_ID_1557954,Human_RBP_ID_1882124,Human_RBP_ID_2561366,Human_RBP_ID_3566047,Human_RBP_ID_4564900,Human_RBP_ID_5190587,Human_RBP_ID_5261363,Human_RBP_ID_5275391,Human_RBP_ID_5421334,Human_RBP_ID_5442854,Human_RBP_ID_5468507,Human_RBP_ID_5499232,Human_RBP_ID_5585542,Human_RBP_ID_6733694,Human_RBP_ID_8096251,Human_RBP_ID_8255913,Human_RBP_ID_8481574,Human_RBP_ID_8831124,Human_RBP_ID_9085570,Human_RBP_ID_9258564,Human_RBP_ID_9291618,Human_RBP_ID_9910911,Human_RBP_ID_13415437,Human_RBP_ID_17009952,Human_RBP_ID_17068497,Human_RBP_ID_17190606,Human_RBP_ID_17267464,Human_RBP_ID_17382686,Human_RBP_ID_17498497,Human_RBP_ID_17695026,Human_RBP_ID_17918675,Human_RBP_ID_18179856,Human_RBP_ID_18200508,Human_RBP_ID_18208356,Human_RBP_ID_18302601,Human_RBP_ID_18440902,Human_RBP_ID_18514808,Human_RBP_ID_18533155,Human_RBP_ID_18726173,Human_RBP_ID_19031282,Human_RBP_ID_20368619,Human_RBP_ID_21891623,Human_RBP_ID_21929794,Human_RBP_ID_22005118,Human_RBP_ID_22391142,Human_RBP_ID_22422473,Human_RBP_ID_22502094,Human_RBP_ID_22810214,Human_RBP_ID_22968254,Human_RBP_ID_23130899,Human_RBP_ID_23277842,Human_RBP_ID_23309457,Human_RBP_ID_23789419,Human_RBP_ID_24418599,Human_RBP_ID_24484013,Human_RBP_ID_24532605,Human_RBP_ID_24538893,Human_RBP_ID_24540133,Human_RBP_ID_25392853,Human_RBP_ID_26474702,Human_RBP_ID_26651774,Human_RBP_ID_26749436,Human_RBP_ID_26987262,Human_RBP_ID_27157449,Human_RBP_ID_27271556,Human_RBP_ID_27466231,Human_RBP_ID_27562296,Human_RBP_ID_27675952 55561 RMVar_ID_55561 Human_SNP_ID_662000482 m1A Human chr19 - 24001575 24001575 24001575 ATATAGACAGCAGGACGGTGGGCATGGAAGTCAGAATCCACTAAGGAGTGTTTAACAACAAAGAA ATATAGACAGCAGGACGGTGGGCATGGAAGTCGGAATCCACTAAGGAGTGTTTAACAACAAAGAA T C RF02543-023 RNACentral:URS00009843EB rRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:24001551..24001575 26863196 MeRIP-seq:(Medium) rs76814135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5421338,Human_RBP_ID_5469637,Human_RBP_ID_18179680 55562 RMVar_ID_55562 Human_SNP_ID_662000800 m1A Human chr19 + 24002176 24002176 24002176 CAGCGCATCAGCCTTCACCTTCATTGCGCCACAGTGGCTTTCGTGCGAGCCCCTGACTCGCACAC CAGCGCATCAGCCTTCACCTTCATTGCGCCACGGTGGCTTTCGTGCGAGCCCCTGACTCGCACAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:24002084..24002220 26863196 MeRIP-seq:(Medium) rs79902636 Functional Loss SNV dbSNP153 33..33 33 - - - 55563 RMVar_ID_55563 Human_SNP_ID_662000801 m1A Human chr19 + 24002176 24002176 24002178 CAGCGCATCAGCCTTCACCTTCATTGCGCCACAGTGGCTTTCGTGCGAGCCCCTGACTCGCACAC CAGCGCATCAGCCTTCACCTTCATTGCGCCACGGCGGCTTTCGTGCGAGCCCCTGACTCGCACAC AGT GGC - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:24002084..24002220 26863196 MeRIP-seq:(Medium) rs796226643 Functional Loss MNV dbSNP153 33..35 33 - - - 55564 RMVar_ID_55564 Human_SNP_ID_662460556 m1A Human chr19 - 27794089 27794089 27794089 TTCCTCAAGCTATCCGCACCACCCTCTCTTCCATTTCATGCGAAGATTGTAGTCCCGCAGCCCTG TTCCTCAAGCTATCCGCACCACCCTCTCTTCCGTTTCATGCGAAGATTGTAGTCCCGCAGCCCTG T C LINC00662,LINC00662:2,LINC00662:3,LINC00662:4 RNACentral:URS00008C3D7F,RNACentral:URS00009BE666,RNACentral:URS00008C2941,RNACentral:URS00009C57DE lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:27794052..27794203 26863196 MeRIP-seq:(Medium) rs948553418 Functional Loss SNV dbSNP153 33..33 33 - - - 55565 RMVar_ID_55565 Human_SNP_ID_662460565 m1A Human chr19 - 27794114 27794114 27794114 ATACCTCCCTCAAGGTATCCGTACCTTCCTCAAGCTATCCGCACCACCCTCTCTTCCATTTCATG ATACCTCCCTCAAGGTATCCGTACCTTCCTCAGGCTATCCGCACCACCCTCTCTTCCATTTCATG T C LINC00662,LINC00662:2,LINC00662:3,LINC00662:4 RNACentral:URS00008C3D7F,RNACentral:URS00009BE666,RNACentral:URS00008C2941,RNACentral:URS00009C57DE lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:27794107..27794198 26863196 MeRIP-seq:(Medium) rs1354938325 Functional Loss SNV dbSNP153 33..33 33 - - - 55566 RMVar_ID_55566 Human_SNP_ID_662948372 m1A Human chr19 - 29606088 29606088 29606088 GGGGTCTTTTCCGCCTGCATCTTTTGGGGGACAGGCAGTAGGGTTGGGGTAAAGGCATGTGGAAT GGGGTCTTTTCCGCCTGCATCTTTTGGGGGACGGGCAGTAGGGTTGGGGTAAAGGCATGTGGAAT T C lnc-C19orf12-12,lnc-C19orf12-12:2,lnc-C19orf12-12:3 RNACentral:URS0000D5A3C8,RNACentral:URS0000D56D69,RNACentral:URS0000D5CAD6 lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:29606040..29606128 26863196 MeRIP-seq:(Medium) rs771954666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6736806 55567 RMVar_ID_55567 Human_SNP_ID_662948387 m1A Human chr19 + 29606129 29606129 29606129 AAAGATGCAGGCGGAAAAGACCCCAGGAAGCGAGCCCACTCCTCCCCACTGCTCAGCAACACCGC AAAGATGCAGGCGGAAAAGACCCCAGGAAGCGTGCCCACTCCTCCCCACTGCTCAGCAACACCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:29605904..29606163 26863196 MeRIP-seq:(Medium) rs1027709304 Functional Loss SNV dbSNP153 33..33 33 - - - 55568 RMVar_ID_55568 Human_SNP_ID_662948484 m1A Human chr19 + 29606322 29606322 29606322 CATCAGAGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGT CATCAGAGAGCGCCGGAAGCGGTCCGAGAATGGAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGT A G POP4 Ensembl:ENSG00000105171 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:29606312..29606398 26863410 MeRIP-seq:(Medium) rs560619277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560161 Human_Splice_Rec_1987599,Human_Splice_Rec_1987601,Human_Splice_Rec_1987613,Human_Splice_Rec_1987621,Human_Splice_Rec_1987633,Human_Splice_Rec_1987643,Human_Splice_Rec_1987653,Human_Splice_Rec_1987665 55569 RMVar_ID_55569 Human_SNP_ID_662948485 m1A Human chr19 + 29606322 29606322 29606322 CATCAGAGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGT CATCAGAGAGCGCCGGAAGCGGTCCGAGAATGTAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGT A T POP4 Ensembl:ENSG00000105171 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:29606312..29606398 26863410 MeRIP-seq:(Medium) rs560619277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560161 Human_Splice_Rec_1987599,Human_Splice_Rec_1987601,Human_Splice_Rec_1987613,Human_Splice_Rec_1987621,Human_Splice_Rec_1987633,Human_Splice_Rec_1987643,Human_Splice_Rec_1987653,Human_Splice_Rec_1987665 55570 RMVar_ID_55570 Human_SNP_ID_662948486 m1A Human chr19 + 29606323 29606323 29606323 ATCAGAGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGTT ATCAGAGAGCGCCGGAAGCGGTCCGAGAATGACGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGTT A C POP4 Ensembl:ENSG00000105171 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:29606307..29606384 26863196 MeRIP-seq:(Medium) rs1478255708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560161 Human_Splice_Rec_1987599,Human_Splice_Rec_1987601,Human_Splice_Rec_1987613,Human_Splice_Rec_1987621,Human_Splice_Rec_1987633,Human_Splice_Rec_1987643,Human_Splice_Rec_1987653,Human_Splice_Rec_1987665 55571 RMVar_ID_55571 Human_SNP_ID_662948487 m1A Human chr19 + 29606323 29606323 29606323 ATCAGAGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGTT ATCAGAGAGCGCCGGAAGCGGTCCGAGAATGAGGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGTT A G POP4 Ensembl:ENSG00000105171 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:29606307..29606384 26863196 MeRIP-seq:(Medium) rs1478255708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560161 Human_Splice_Rec_1987599,Human_Splice_Rec_1987601,Human_Splice_Rec_1987613,Human_Splice_Rec_1987621,Human_Splice_Rec_1987633,Human_Splice_Rec_1987643,Human_Splice_Rec_1987653,Human_Splice_Rec_1987665 55572 RMVar_ID_55572 Human_SNP_ID_662948493 m1A Human chr19 + 29606328 29606328 29606328 AGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTAAGCGGGGCCGCGAAGTTGGAGAGGGTTGGGGA AGAGCGCCGGAAGCGGTCCGAGAATGAAGAGTTAGCGGGGCCGCGAAGTTGGAGAGGGTTGGGGA A T POP4 Ensembl:ENSG00000105171 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:29606324..29606407 26863196 MeRIP-seq:(Medium) rs1463279386 Functional Loss SNV dbSNP153 33..33 33 - - - 55573 RMVar_ID_55573 Human_SNP_ID_662949197 m1A Human chr19 + 29608683 29608680 29608684 CCCCAGGTGTGATCTACCATGCATTGTCTCAGAAAGAGGCGAATGACTCCGATGTCCAGGTCAGT CCCCAGGTGTGATCTACCATGCATTGTCTC____AGAGGCGAATGACTCCGATGTCCAGGTCAGT CAGAA C POP4 Ensembl:ENSG00000105171 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:29606301..29608761 26863196 MeRIP-seq:(Medium) rs1568293785 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_1558725,Human_RBP_ID_4565286,Human_RBP_ID_19089854 Human_Splice_Rec_1987600,Human_Splice_Rec_1987602,Human_Splice_Rec_1987603,Human_Splice_Rec_1987614,Human_Splice_Rec_1987615,Human_Splice_Rec_1987622,Human_Splice_Rec_1987623,Human_Splice_Rec_1987634,Human_Splice_Rec_1987635,Human_Splice_Rec_1987644,Human_Splice_Rec_1987645,Human_Splice_Rec_1987654,Human_Splice_Rec_1987655,Human_Splice_Rec_1987666,Human_Splice_Rec_1987667,Human_Splice_Rec_1987670,Human_Splice_Rec_1987671,Human_Splice_Rec_1987678,Human_Splice_Rec_1987679 55574 RMVar_ID_55574 Human_SNP_ID_662949706 m1A Human chr19 + 29610455 29610455 29610455 GCGGGCCGAGGCCTTCGTGAGGGCCTTCCTGAAGCGCAGCACGCCCCGCATGAGCCCGCAGGCCC GCGGGCCGAGGCCTTCGTGAGGGCCTTCCTGAGGCGCAGCACGCCCCGCATGAGCCCGCAGGCCC A G POP4 Ensembl:ENSG00000105171 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:29610381..29610512;chr19:29610352..29610560;chr19:29610367..29610535 26863196 MeRIP-seq:(Medium) rs769536040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558316,Human_RBP_ID_9380862,Human_RBP_ID_19096128,Human_RBP_ID_22446633 Human_Splice_Rec_1987604,Human_Splice_Rec_1987616,Human_Splice_Rec_1987624,Human_Splice_Rec_1987646,Human_Splice_Rec_1987668,Human_Splice_Rec_1987672,Human_Splice_Rec_1987682,Human_Splice_Rec_1987690 55575 RMVar_ID_55575 Human_SNP_ID_662963414 m1A Human chr19 + 29665501 29665490 29665501 GTGGACTCGAGGGCTGGGCGCGGGGCCGGCGCAGAAGGTGAGTCCCCCCACCGTCCCCCGGCCGG GTGGACTCGAGGGCTGGGCGCG___________GAAGGTGAGTCCCCCCACCGTCCCCCGGCCGG GGGGCCGGCGCA G PLEKHF1 Ensembl:ENSG00000166289 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:29665447..29665593;chr19:29665445..29665659 26863196 MeRIP-seq:(Medium) rs1290529143 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_4558317 Human_Splice_Rec_1987707 55576 RMVar_ID_55576 Human_SNP_ID_662963416 m1A Human chr19 + 29665503 29665500 29665503 GGACTCGAGGGCTGGGCGCGGGGCCGGCGCAGAAGGTGAGTCCCCCCACCGTCCCCCGGCCGGGC GGACTCGAGGGCTGGGCGCGGGGCCGGCGC___AGGTGAGTCCCCCCACCGTCCCCCGGCCGGGC CAGA C PLEKHF1 Ensembl:ENSG00000166289 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:29665468..29665593 26863196 MeRIP-seq:(Medium) rs758558065 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4558317 Human_Splice_Rec_1987707 55577 RMVar_ID_55577 Human_SNP_ID_662963417 m1A Human chr19 + 29665501 29665501 29665501 GTGGACTCGAGGGCTGGGCGCGGGGCCGGCGCAGAAGGTGAGTCCCCCCACCGTCCCCCGGCCGG GTGGACTCGAGGGCTGGGCGCGGGGCCGGCGCGGAAGGTGAGTCCCCCCACCGTCCCCCGGCCGG A G PLEKHF1 Ensembl:ENSG00000166289 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:29665447..29665593;chr19:29665445..29665659 26863196 MeRIP-seq:(Medium) rs1306455526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558317 Human_Splice_Rec_1987707 55578 RMVar_ID_55578 Human_SNP_ID_662965438 m1A Human chr19 - 29673949 29673949 29673949 TGCGGCACTCTTTGGTCAGCACGCCCTCGCCCAGCAGCACTCGGCCTGGCAGCGCCAGCGGCTGC TGCGGCACTCTTTGGTCAGCACGCCCTCGCCCCGCAGCACTCGGCCTGGCAGCGCCAGCGGCTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:29673832..29674050 26863196 MeRIP-seq:(Medium) rs1000482462 Functional Loss SNV dbSNP153 33..33 33 - - - 55579 RMVar_ID_55579 Human_SNP_ID_662974877 m1A Human chr19 - 29708245 29708245 29708245 GCGGCCCACCGGGACTCGCCGTTGGTAAGTGCAGGTGTCTCACAGAGATAGCCAGCCTCGGGGAT GCGGCCCACCGGGACTCGCCGTTGGTAAGTGCGGGTGTCTCACAGAGATAGCCAGCCTCGGGGAT T C C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:29708243..29708315 26863196 MeRIP-seq:(Medium) rs771382701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911128,Human_RBP_ID_8482358 55580 RMVar_ID_55580 Human_SNP_ID_662974878 m1A Human chr19 - 29708245 29708245 29708245 GCGGCCCACCGGGACTCGCCGTTGGTAAGTGCAGGTGTCTCACAGAGATAGCCAGCCTCGGGGAT GCGGCCCACCGGGACTCGCCGTTGGTAAGTGCCGGTGTCTCACAGAGATAGCCAGCCTCGGGGAT T G C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:29708243..29708315 26863196 MeRIP-seq:(Medium) rs771382701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911128,Human_RBP_ID_8482358 55581 RMVar_ID_55581 Human_SNP_ID_662976716 m1A Human chr19 - 29715172 29715172 29715172 GGGGAGCCCGGGGCCTGCCAGGCCCGGGCTGCAGCCGCGTCTGATCGCCGAGCGCGCCGCGTAGA GGGGAGCCCGGGGCCTGCCAGGCCCGGGCTGCCGCCGCGTCTGATCGCCGAGCGCGCCGCGTAGA T G C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:29715123..29715235 26863196 MeRIP-seq:(Medium) rs1360784478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241620,Human_RBP_ID_4516016,Human_RBP_ID_8482360,Human_RBP_ID_18420900 Human_Splice_Rec_1987719,Human_Splice_Rec_1987723,Human_Splice_Rec_1987725,Human_Splice_Rec_1987737 55582 RMVar_ID_55582 Human_SNP_ID_663003177 m1A Human chr19 - 29812097 29812076 29812097 GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCGACGGCAGTGGCGGCGGCGGCGCCGGGAGTCGGC GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCG_____________________CCGGGAGTCGGC GCGCCGCCGCCGCCACTGCCGT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:29811947..29812577 26863410 MeRIP-seq:(Medium) rs998974050 Functional Loss DEL dbSNP153 33..53 33 - - - 55583 RMVar_ID_55583 Human_SNP_ID_663003182 m1A Human chr19 - 29812097 29812079 29812097 GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCGACGGCAGTGGCGGCGGCGGCGCCGGGAGTCGGC GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCG__________________GCGCCGGGAGTCGGC CCGCCGCCGCCACTGCCGT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:29811947..29812577 26863410 MeRIP-seq:(Medium) rs1165351482 Functional Loss DEL dbSNP153 33..50 33 - - - 55584 RMVar_ID_55584 Human_SNP_ID_663003190 m1A Human chr19 - 29812097 29812096 29812097 GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCGACGGCAGTGGCGGCGGCGGCGCCGGGAGTCGGC GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCG_CGGCAGTGGCGGCGGCGGCGCCGGGAGTCGGC GT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:29811947..29812577 26863410 MeRIP-seq:(Medium) rs1555724796 Functional Loss DEL dbSNP153 33..33 33 - - - 55585 RMVar_ID_55585 Human_SNP_ID_663003196 m1A Human chr19 + 29812118 29812118 29812118 CGCCACTGCCGTCGCCGCCGCCGCCTGCCGGGACTGGAGCGCGCCGTCCGCCGCGGACAAGACCC CGCCACTGCCGTCGCCGCCGCCGCCTGCCGGGGCTGGAGCGCGCCGTCCGCCGCGGACAAGACCC A G CCNE1 Ensembl:ENSG00000105173 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:29812017..29812239 26863196 MeRIP-seq:(Medium) rs1334183924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559474 Human_Splice_Rec_1987745,Human_Splice_Rec_1987767 55586 RMVar_ID_55586 Human_SNP_ID_663003204 m1A Human chr19 - 29812132 29812131 29812132 CAGTAGACTCACCAGGGTCTTGTCCGCGGCGGACGGCGCGCTCCAGTCCCGGCAGGCGGCGGCGG CAGTAGACTCACCAGGGTCTTGTCCGCGGCGG_CGGCGCGCTCCAGTCCCGGCAGGCGGCGGCGG GT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:29812040..29812148 26863410 MeRIP-seq:(Medium) rs1403529386 Functional Loss DEL dbSNP153 33..33 33 - - - 55587 RMVar_ID_55587 Human_SNP_ID_663003459 m1A Human chr19 + 29812721 29812721 29812721 GGATGCGAAGGAGCGGGACACCATGAAGGAGGACGGCGGCGCGGAGTTCTCGGCTCGCTCCAGGA GGATGCGAAGGAGCGGGACACCATGAAGGAGGCCGGCGGCGCGGAGTTCTCGGCTCGCTCCAGGA A C CCNE1 Ensembl:ENSG00000105173 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:29812015..29812994 26863196 MeRIP-seq:(Medium) rs1469198229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4516042,Human_RBP_ID_19096130,Human_RBP_ID_26784042 Human_Splice_Rec_1987748,Human_Splice_Rec_1987749,Human_Splice_Rec_1987770,Human_Splice_Rec_1987771,Human_Splice_Rec_1987781,Human_Splice_Rec_1987799,Human_Splice_Rec_1987815 55588 RMVar_ID_55588 Human_SNP_ID_663003460 m1A Human chr19 + 29812721 29812721 29812721 GGATGCGAAGGAGCGGGACACCATGAAGGAGGACGGCGGCGCGGAGTTCTCGGCTCGCTCCAGGA GGATGCGAAGGAGCGGGACACCATGAAGGAGGGCGGCGGCGCGGAGTTCTCGGCTCGCTCCAGGA A G CCNE1 Ensembl:ENSG00000105173 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:29812015..29812994 26863196 MeRIP-seq:(Medium) rs1469198229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4516042,Human_RBP_ID_19096130,Human_RBP_ID_26784042 Human_Splice_Rec_1987748,Human_Splice_Rec_1987749,Human_Splice_Rec_1987770,Human_Splice_Rec_1987771,Human_Splice_Rec_1987781,Human_Splice_Rec_1987799,Human_Splice_Rec_1987815 55589 RMVar_ID_55589 Human_SNP_ID_663039313 m1A Human chr19 - 29942301 29942301 29942301 GCGGGCTCCGAGTAGCAGGCCGCCTGCCAGGTACCGAGACGCCTCTCCGGTGCGGGCCCAGCCAG GCGGGCTCCGAGTAGCAGGCCGCCTGCCAGGTGCCGAGACGCCTCTCCGGTGCGGGCCCAGCCAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:29942251..29942411 26863196 MeRIP-seq:(Medium) rs1328773095 Functional Loss SNV dbSNP153 33..33 33 - - - 55590 RMVar_ID_55590 Human_SNP_ID_663039356 m1A Human chr19 - 29942427 29942413 29942427 GCCCGCCCTCAGGCACCGCGCGCCCCGCGCCCAGGAGGCCGCGCCCGCCGCCGCCGCTGCTGTTC GCCCGCCCTCAGGCACCGCGCGCCCCGCGCCC______________GCCGCCGCCGCTGCTGTTC CGGGCGCGGCCTCCT C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:29942317..29942506 26863410 MeRIP-seq:(Medium) rs1568406621 Functional Loss DEL dbSNP153 33..46 33 - - - 55591 RMVar_ID_55591 Human_SNP_ID_663039397 m1A Human chr19 - 29942494 29942494 29942494 GCGGCGTGTGAGTCCTGAACCAGCGCCTGCGCAGGCGGCGCGGCCGGCAGTTGCCCAGCGCCCGC GCGGCGTGTGAGTCCTGAACCAGCGCCTGCGCGGGCGGCGCGGCCGGCAGTTGCCCAGCGCCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:29942317..29942517;chr19:29942291..29958028 26863410 MeRIP-seq:(Medium) rs978606559 Functional Loss SNV dbSNP153 33..33 33 - - - 55592 RMVar_ID_55592 Human_SNP_ID_165593457 m1A Human chr3 - 180912537 180912537 180912537 GGGATCCCCCGCCCTTCACCCCTGGGGTCTCAACGTGCCGCCCCGACTCTCCAGGTGGGATCCCT GGGATCCCCCGCCCTTCACCCCTGGGGTCTCAGCGTGCCGCCCCGACTCTCCAGGTGGGATCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:180912486..180912580 26863196 MeRIP-seq:(Medium) rs762017615 Functional Loss SNV dbSNP153 33..33 33 - - - 55593 RMVar_ID_55593 Human_SNP_ID_165593568 m1A Human chr3 + 180912734 180912734 180912734 TGGAGGTTCGCGGCTCTAACGGGGCTTTCTACAAGGTACTGACCGTTTTGCCACTTTGTCGAGTG TGGAGGTTCGCGGCTCTAACGGGGCTTTCTACGAGGTACTGACCGTTTTGCCACTTTGTCGAGTG A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:180912720..180912807 26863196 MeRIP-seq:(Medium) rs768543445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032114,Human_RBP_ID_1311463,Human_RBP_ID_4757574,Human_RBP_ID_8566445,Human_RBP_ID_9260934,Human_RBP_ID_19118863,Human_RBP_ID_23026656,Human_RBP_ID_24384049 Human_Splice_Rec_510525,Human_Splice_Rec_510559,Human_Splice_Rec_510587,Human_Splice_Rec_510589,Human_Splice_Rec_510621,Human_Splice_Rec_510627,Human_Splice_Rec_510653,Human_Splice_Rec_510681,Human_Splice_Rec_510711,Human_Splice_Rec_510739 55594 RMVar_ID_55594 Human_SNP_ID_165593759 m1A Human chr3 - 180913241 180913241 180913241 TTCTCCTCAGACACTAAAGATTTGTTGGCCCAAAACTCAAATACAAGGGTGAATTCCAAAGATTC TTCTCCTCAGACACTAAAGATTTGTTGGCCCACAACTCAAATACAAGGGTGAATTCCAAAGATTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:180913117..180913300 26863196 MeRIP-seq:(Medium) rs1017759042 Functional Loss SNV dbSNP153 33..33 33 - - - 55595 RMVar_ID_55595 Human_SNP_ID_165599928 m1A Human chr3 + 180935128 180935128 180935128 ATATATTTTTAAGTTGTTAATACACCTTTTCTAATCCTTCAGTTGGCAACCAGAACGCCAGGTTC ATATATTTTTAAGTTGTTAATACACCTTTTCTCATCCTTCAGTTGGCAACCAGAACGCCAGGTTC A C FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:180935126..180935225 32194978 MeRIP-seq:(Medium) rs773461183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7164225 RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_3776,RMVar_hsa_circ_269031,RMVar_hsa_circ_291789,RMVar_hsa_circ_335471,RMVar_hsa_circ_347606,RMVar_hsa_circ_278355,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_22447,RMVar_hsa_circ_223014,RMVar_hsa_circ_223015,RMVar_hsa_circ_223016 55596 RMVar_ID_55596 Human_SNP_ID_165599929 m1A Human chr3 + 180935128 180935128 180935128 ATATATTTTTAAGTTGTTAATACACCTTTTCTAATCCTTCAGTTGGCAACCAGAACGCCAGGTTC ATATATTTTTAAGTTGTTAATACACCTTTTCTGATCCTTCAGTTGGCAACCAGAACGCCAGGTTC A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:180935126..180935225 32194978 MeRIP-seq:(Medium) rs773461183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7164225 RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_3776,RMVar_hsa_circ_269031,RMVar_hsa_circ_291789,RMVar_hsa_circ_335471,RMVar_hsa_circ_347606,RMVar_hsa_circ_278355,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_22447,RMVar_hsa_circ_223014,RMVar_hsa_circ_223015,RMVar_hsa_circ_223016 55597 RMVar_ID_55597 Human_SNP_ID_165608694 m1A Human chr3 + 180968130 180968130 180968130 AAAGACGAGCTGAGTGATTGGTCATTGGCAGGAGAAGATGATCGAGACAGCCGACATCAGCGTGA AAAGACGAGCTGAGTGATTGGTCATTGGCAGGGGAAGATGATCGAGACAGCCGACATCAGCGTGA A G FXR1 Ensembl:ENSG00000114416 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:180968079..180968228 26863196 MeRIP-seq:(Medium) rs750281049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14740366,Human_RBP_ID_17703390,Human_RBP_ID_23987555,Human_RBP_ID_26347431 Human_Splice_Rec_510552,Human_Splice_Rec_510580,Human_Splice_Rec_510614,Human_Splice_Rec_510648,Human_Splice_Rec_510676,Human_Splice_Rec_510706,Human_Splice_Rec_510734,Human_Splice_Rec_510774,Human_Splice_Rec_510808,Human_Splice_Rec_510816 RMVar_hsa_circ_275326,RMVar_hsa_circ_267648,RMVar_hsa_circ_326172,RMVar_hsa_circ_11916,RMVar_hsa_circ_71478,RMVar_hsa_circ_83128,RMVar_hsa_circ_223022,RMVar_hsa_circ_351430,RMVar_hsa_circ_99734,RMVar_hsa_circ_223025,RMVar_hsa_circ_14321,RMVar_hsa_circ_294834,RMVar_hsa_circ_223026 55598 RMVar_ID_55598 Human_SNP_ID_165610757 m1A Human chr3 + 180976157 180976157 180976157 AAAGATGTGATTGAAGAGCATGGTCCTTCAGAAAAGGCAATAAACGGCCCAACTAGTGCTTCTGG AAAGATGTGATTGAAGAGCATGGTCCTTCAGAGAAGGCAATAAACGGCCCAACTAGTGCTTCTGG A G FXR1 Ensembl:ENSG00000114416 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:180976128..180976278 32194978 MeRIP-seq:(Medium) rs201161602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69773,Human_RBP_ID_7164649,Human_RBP_ID_9260951 Human_Splice_Rec_510558,Human_Splice_Rec_510586,Human_Splice_Rec_510620,Human_Splice_Rec_510652,Human_Splice_Rec_510680,Human_Splice_Rec_510710,Human_Splice_Rec_510738,Human_Splice_Rec_510780,Human_Splice_Rec_510826 55599 RMVar_ID_55599 Human_SNP_ID_165614402 m1A Human chr3 + 180989657 180989657 180989657 TTCCACCGGGAGCACGGCTCATCCCAGCTCAGAGGCCGCGGCCAACACCTGCACGCCTTTACCAG TTCCACCGGGAGCACGGCTCATCCCAGCTCAGTGGCCGCGGCCAACACCTGCACGCCTTTACCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:180989607..180989702 26863196 MeRIP-seq:(Medium) rs1259588675 Functional Loss SNV dbSNP153 33..33 33 - - - 55600 RMVar_ID_55600 Human_SNP_ID_166042060 m1A Human chr3 - 182793575 182793575 182793575 CCCCATCCCGCGGCGTCGGCCCCGAGTCCTACAGGCGCGGCCCCGGCGCCGCCCCCGCCCGGCGC CCCCATCCCGCGGCGTCGGCCCCGAGTCCTACGGGCGCGGCCCCGGCGCCGCCCCCGCCCGGCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:182793526..182793683 26863196 MeRIP-seq:(Medium) rs1209981926 Functional Loss SNV dbSNP153 33..33 33 - - - 55601 RMVar_ID_55601 Human_SNP_ID_166087826 m1A Human chr3 - 182980265 182980265 182980265 GCGCAGCCGCTACGCGAGAGCCGAGGAGGCGGAGCGGAGCCGGGCCTAGTCGGGAGCCCCGGGGA GCGCAGCCGCTACGCGAGAGCCGAGGAGGCGGGGCGGAGCCGGGCCTAGTCGGGAGCCCCGGGGA T C DCUN1D1 Ensembl:ENSG00000043093 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:182980253..182980567 26863196 MeRIP-seq:(Medium) rs1374218000 Functional Loss SNV dbSNP153 33..33 33 - - - 55602 RMVar_ID_55602 Human_SNP_ID_166087944 m1A Human chr3 + 182980541 182980541 182980541 CTCCCCTCCTCCTCCGGCTCCGCAGCGAATGGACGGCGGCGGCGGCGGCGGCTCCTCTCACGGGC CTCCCCTCCTCCTCCGGCTCCGCAGCGAATGGGCGGCGGCGGCGGCGGCGGCTCCTCTCACGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:182980452..182980566;chr3:182980295..182980557 26863196 MeRIP-seq:(Medium) rs1553846460 Functional Loss SNV dbSNP153 33..33 33 - - - 55603 RMVar_ID_55603 Human_SNP_ID_166109114 m1A Human chr3 - 183071122 183071122 183071122 TATGTTGTAGTCATAATCATCTTTTCTCTCTTAGGGAATGAGGATTGTTAGATCAGAACAAGAAT TATGTTGTAGTCATAATCATCTTTTCTCTCTTGGGGAATGAGGATTGTTAGATCAGAACAAGAAT T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:183071100..183071175 26863196 MeRIP-seq:(Medium) rs772395858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_513428 Clinvar_Rec_144 RMVar_hsa_circ_62079,RMVar_hsa_circ_115816,RMVar_hsa_circ_223084,RMVar_hsa_circ_73887,RMVar_hsa_circ_54092,RMVar_hsa_circ_24668,RMVar_hsa_circ_223087,RMVar_hsa_circ_35109,RMVar_hsa_circ_298979,RMVar_hsa_circ_356202,RMVar_hsa_circ_223092,RMVar_hsa_circ_223090,RMVar_hsa_circ_314110,RMVar_hsa_circ_223089,RMVar_hsa_circ_295323,RMVar_hsa_circ_365888,RMVar_hsa_circ_37937,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_354997,RMVar_hsa_circ_223091,RMVar_hsa_circ_333240,RMVar_hsa_circ_275642,RMVar_hsa_circ_223094,RMVar_hsa_circ_223095,RMVar_hsa_circ_223093 55604 RMVar_ID_55604 Human_SNP_ID_166114640 m1A Human chr3 + 183094601 183094601 183094601 TGTGTACTTCATGGTTCTTTGCCTCCACACCCATGTCCTATAACATAAATCCAAAAGGAATTACA TGTGTACTTCATGGTTCTTTGCCTCCACACCCGTGTCCTATAACATAAATCCAAAAGGAATTACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:183092480..183098542 26863196 MeRIP-seq:(Medium) rs761132865 Functional Loss SNV dbSNP153 33..33 33 - - - 55605 RMVar_ID_55605 Human_SNP_ID_166114641 m1A Human chr3 - 183094602 183094602 183094602 TTGTAATTCCTTTTGGATTTATGTTATAGGACATGGGTGTGGAGGCAAAGAACCATGAAGTACAC TTGTAATTCCTTTTGGATTTATGTTATAGGACGTGGGTGTGGAGGCAAAGAACCATGAAGTACAC T C MCCC1 Ensembl:ENSG00000078070 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183092499..183098542 26863196 MeRIP-seq:(Medium) rs1207428301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936072,Human_RBP_ID_3965703,Human_RBP_ID_19011083 Human_Splice_Rec_513128,Human_Splice_Rec_513129,Human_Splice_Rec_513164,Human_Splice_Rec_513165,Human_Splice_Rec_513198,Human_Splice_Rec_513199,Human_Splice_Rec_513230,Human_Splice_Rec_513231,Human_Splice_Rec_513264,Human_Splice_Rec_513265,Human_Splice_Rec_513304,Human_Splice_Rec_513305,Human_Splice_Rec_513340,Human_Splice_Rec_513341,Human_Splice_Rec_513370,Human_Splice_Rec_513371,Human_Splice_Rec_513414,Human_Splice_Rec_513415,Human_Splice_Rec_513422,Human_Splice_Rec_513423,Human_Splice_Rec_513430,Human_Splice_Rec_513431,Human_Splice_Rec_513439 RMVar_hsa_circ_223096,RMVar_hsa_circ_333240,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_293717,RMVar_hsa_circ_223099,RMVar_hsa_circ_273971 55606 RMVar_ID_55606 Human_SNP_ID_166115785 m1A Human chr3 - 183099329 183099329 183099329 TGCCGCCGAGGTGGGTGGAGGGGCCATGGCTCAGTGGGCAGAGGCGGGAGCGAGGGGTGCACGGA TGCCGCCGAGGTGGGTGGAGGGGCCATGGCTCTGTGGGCAGAGGCGGGAGCGAGGGGTGCACGGA T A MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:183099328..183099485 26863196 MeRIP-seq:(Medium) rs1290242327 Functional Loss SNV dbSNP153 33..33 33 - - - 55607 RMVar_ID_55607 Human_SNP_ID_166115786 m1A Human chr3 - 183099329 183099329 183099329 TGCCGCCGAGGTGGGTGGAGGGGCCATGGCTCAGTGGGCAGAGGCGGGAGCGAGGGGTGCACGGA TGCCGCCGAGGTGGGTGGAGGGGCCATGGCTCGGTGGGCAGAGGCGGGAGCGAGGGGTGCACGGA T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:183099328..183099485 26863196 MeRIP-seq:(Medium) rs1290242327 Functional Loss SNV dbSNP153 33..33 33 - - - 55608 RMVar_ID_55608 Human_SNP_ID_166115867 m1A Human chr3 + 183099449 183099449 183099449 CGACACCGCAGAGGCCGCCGCCATGTCCCTGGAGCCCGGCCACTCCGTGACTCCCCAGTACAGAG CGACACCGCAGAGGCCGCCGCCATGTCCCTGGGGCCCGGCCACTCCGTGACTCCCCAGTACAGAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:183099326..183099486 26863196 MeRIP-seq:(Medium) rs1349820850 Functional Loss SNV dbSNP153 33..33 33 - - - 55609 RMVar_ID_55609 Human_SNP_ID_166115876 m1A Human chr3 - 183099460 183099460 183099460 GACGCAGCTGCCTCTGTACTGGGGAGTCACGGAGTGGCCGGGCTCCAGGGACATGGCGGCGGCCT GACGCAGCTGCCTCTGTACTGGGGAGTCACGGCGTGGCCGGGCTCCAGGGACATGGCGGCGGCCT T G MCCC1 Ensembl:ENSG00000078070 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:183099376..183099525 26863196 MeRIP-seq:(Medium) rs890799240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757580,Human_RBP_ID_18413281,Human_RBP_ID_18424099 55610 RMVar_ID_55610 Human_SNP_ID_166115882 m1A Human chr3 - 183099464 183099464 183099464 GTGGGACGCAGCTGCCTCTGTACTGGGGAGTCACGGAGTGGCCGGGCTCCAGGGACATGGCGGCG GTGGGACGCAGCTGCCTCTGTACTGGGGAGTCTCGGAGTGGCCGGGCTCCAGGGACATGGCGGCG T A MCCC1 Ensembl:ENSG00000078070 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:183099185..183099575 26863196 MeRIP-seq:(Medium) rs11540930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757580,Human_RBP_ID_18413281,Human_RBP_ID_18424099 55611 RMVar_ID_55611 Human_SNP_ID_166115883 m1A Human chr3 - 183099464 183099464 183099464 GTGGGACGCAGCTGCCTCTGTACTGGGGAGTCACGGAGTGGCCGGGCTCCAGGGACATGGCGGCG GTGGGACGCAGCTGCCTCTGTACTGGGGAGTCGCGGAGTGGCCGGGCTCCAGGGACATGGCGGCG T C MCCC1 Ensembl:ENSG00000078070 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:183099185..183099575 26863196 MeRIP-seq:(Medium) rs11540930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757580,Human_RBP_ID_18413281,Human_RBP_ID_18424099 55612 RMVar_ID_55612 Human_SNP_ID_166163763 m1A Human chr3 - 183296461 183296461 183296461 CGAATAGACAAGATGGGAGAGCCTTTCCAGACAGGAGGAACAGCATGTGCAAAGGCTTCAGGGCT CGAATAGACAAGATGGGAGAGCCTTTCCAGACGGGAGGAACAGCATGTGCAAAGGCTTCAGGGCT T C MCF2L2 Ensembl:ENSG00000053524 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183296349..183296472 26863196 MeRIP-seq:(Medium) rs1228589911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1134,RMVar_hsa_circ_127601,RMVar_hsa_circ_223100,RMVar_hsa_circ_103678,RMVar_hsa_circ_299377,RMVar_hsa_circ_223105,RMVar_hsa_circ_84819,RMVar_hsa_circ_53497,RMVar_hsa_circ_223110,RMVar_hsa_circ_296165,RMVar_hsa_circ_309586,RMVar_hsa_circ_288030,RMVar_hsa_circ_5372,RMVar_hsa_circ_223112,RMVar_hsa_circ_223111,RMVar_hsa_circ_35534,RMVar_hsa_circ_13922,RMVar_hsa_circ_331692,RMVar_hsa_circ_223116 55613 RMVar_ID_55613 Human_SNP_ID_166182887 m1A Human chr3 + 183374030 183374030 183374030 TCCATCCCTTCCTATCCAGTTCTCATGCCATCATCCCTCTTCGTTTTGCACCTGTCTCAGTGTAG TCCATCCCTTCCTATCCAGTTCTCATGCCATCGTCCCTCTTCGTTTTGCACCTGTCTCAGTGTAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183373933..183374135 26863196 MeRIP-seq:(Medium) rs970553417 Functional Loss SNV dbSNP153 33..33 33 - - - 55614 RMVar_ID_55614 Human_SNP_ID_166195743 m1A Human chr3 - 183428513 183428513 183428513 GCAGGGAAAGGTGCGCAGCGTTCCCGACCCCAAAACGAGCGGCGCTTGGGAGCGTGCGTGCCTCC GCAGGGAAAGGTGCGCAGCGTTCCCGACCCCAGAACGAGCGGCGCTTGGGAGCGTGCGTGCCTCC T C MCF2L2 Ensembl:ENSG00000053524 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183428465..183428550 26863196 MeRIP-seq:(Medium) rs1255313007 Functional Loss SNV dbSNP153 33..33 33 - - - 55615 RMVar_ID_55615 Human_SNP_ID_166263570 m1A Human chr3 - 183697995 183697995 183697995 CGGCCGGTCCCTTCCTGCGCCCGCCAACACTCACCCTTTCTCCGGGTCTCCGGCTGCAGCGCGGG CGGCCGGTCCCTTCCTGCGCCCGCCAACACTCCCCCTTTCTCCGGGTCTCCGGCTGCAGCGCGGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:183697861..183698095 26863196 MeRIP-seq:(Medium) rs1014254464 Functional Loss SNV dbSNP153 33..33 33 - - - 55616 RMVar_ID_55616 Human_SNP_ID_166272876 m1A Human chr3 - 183730947 183730947 183730947 CACCCCAATCCAACTATTCTTTGACTTCACGGAGACTTCTATTTCTTGCCCACAAAACTTTTCAC CACCCCAATCCAACTATTCTTTGACTTCACGGGGACTTCTATTTCTTGCCCACAAAACTTTTCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183730899..183731020 26863196 MeRIP-seq:(Medium) rs987526593 Functional Loss SNV dbSNP153 33..33 33 - - - 55617 RMVar_ID_55617 Human_SNP_ID_166285032 m1A Human chr3 - 183776000 183775976 183776000 GTTCCTCCTCCTCCTCCTGTGCTGCCGCCTCCACCGCTGCCACTGCCGCCTCCTCCTCCTCCTCC GTTCCTCCTCCTCCTCCTGTGCTGCCGCCTCC________________________TCCTCCTCC AGGAGGAGGCGGCAGTGGCAGCGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:183775952..183776070;chr3:183775949..183776079 26863196 MeRIP-seq:(Medium) rs1560301114 Functional Loss DEL dbSNP153 33..56 33 - - - 55618 RMVar_ID_55618 Human_SNP_ID_166285060 m1A Human chr3 - 183776000 183776000 183776000 GTTCCTCCTCCTCCTCCTGTGCTGCCGCCTCCACCGCTGCCACTGCCGCCTCCTCCTCCTCCTCC GTTCCTCCTCCTCCTCCTGTGCTGCCGCCTCCCCCGCTGCCACTGCCGCCTCCTCCTCCTCCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:183775952..183776070;chr3:183775949..183776079 26863196 MeRIP-seq:(Medium) rs150730708 Functional Loss SNV dbSNP153 33..33 33 - - - 55619 RMVar_ID_55619 Human_SNP_ID_166295218 m1A Human chr3 - 183812154 183812152 183812155 TTGGCACACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTTCCTGCCTCAGCCTCCCGAGTAG TTGGCACACTGCAACCTCCGCCTCCTGGGTT___GTGATTCTTCCTGCCTCAGCCTCCCGAGTAG CTTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:183812026..183812177 32194978 MeRIP-seq:(Medium) rs1281545942 Functional Loss DEL dbSNP153 32..34 33 - - - 55620 RMVar_ID_55620 Human_SNP_ID_166299386 m1A Human chr3 + 183825513 183825513 183825513 CGGAGCGGTCCAGCTGGTTCCAGCGCCGCGCCAGGCAGCACAGGCGGCTGATACAGGGCCACGCC CGGAGCGGTCCAGCTGGTTCCAGCGCCGCGCCTGGCAGCACAGGCGGCTGATACAGGGCCACGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:183825464..183825562 26863196 MeRIP-seq:(Medium) rs1275715279 Functional Loss SNV dbSNP153 33..33 33 - - - 55621 RMVar_ID_55621 Human_SNP_ID_166300448 m1A Human chr3 - 183829620 183829620 183829620 AATCTGGCATGAAATAAGGACTAATGGCCCCAAAAAAGGAGGTGGCTCTAAGTAAAACTGGGATT AATCTGGCATGAAATAAGGACTAATGGCCCCACAAAAGGAGGTGGCTCTAAGTAAAACTGGGATT T G AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:183829467..183829665 32194978 MeRIP-seq:(Medium) rs752311820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596297,Human_RBP_ID_1957238,Human_RBP_ID_23988794 Human_Splice_Rec_514096,Human_Splice_Rec_514116,Human_Splice_Rec_514136,Human_Splice_Rec_514142,Human_Splice_Rec_514146,Human_Splice_Rec_514156,Human_Splice_Rec_514172,Human_Splice_Rec_514186,Human_Splice_Rec_514206,Human_Splice_Rec_514224 Human_miRNA_ID_2015147 RMVar_hsa_circ_111081,RMVar_hsa_circ_122460,RMVar_hsa_circ_123715,RMVar_hsa_circ_112442,RMVar_hsa_circ_223256,RMVar_hsa_circ_223258,RMVar_hsa_circ_102949,RMVar_hsa_circ_223259,RMVar_hsa_circ_223257,RMVar_hsa_circ_223255 55622 RMVar_ID_55622 Human_SNP_ID_166309813 m1A Human chr3 - 183868030 183868030 183868030 AGGTTTAACTTCTTTATTCAACAAAAATGCGGATTCAGAAAAGCACCCAGGAAGGTTGAACCTCG AGGTTTAACTTCTTTATTCAACAAAAATGCGGCTTCAGAAAAGCACCCAGGAAGGTTGAACCTCG T G AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:183867980..183884790 32194978 MeRIP-seq:(Medium) rs765027346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1623115,Human_RBP_ID_1957257,Human_RBP_ID_9334357,Human_RBP_ID_14743767,Human_RBP_ID_19011091 Human_Splice_Rec_514046,Human_Splice_Rec_514080,Human_Splice_Rec_514098,Human_Splice_Rec_514118,Human_Splice_Rec_514158,Human_Splice_Rec_514174,Human_Splice_Rec_514188,Human_Splice_Rec_514208,Human_Splice_Rec_514226,Human_Splice_Rec_514240 Human_miRNA_ID_2038998,Human_miRNA_ID_3017978 RMVar_hsa_circ_6555,RMVar_hsa_circ_102949,RMVar_hsa_circ_223259,RMVar_hsa_circ_274454,RMVar_hsa_circ_294498,RMVar_hsa_circ_223268,RMVar_hsa_circ_223260,RMVar_hsa_circ_372607,RMVar_hsa_circ_223271,RMVar_hsa_circ_223274,RMVar_hsa_circ_341657,RMVar_hsa_circ_294398,RMVar_hsa_circ_223273,RMVar_hsa_circ_270165,RMVar_hsa_circ_346883,RMVar_hsa_circ_292412 55623 RMVar_ID_55623 Human_SNP_ID_166314532 m1A Human chr3 - 183884822 183884822 183884822 TTGGGAAGATGGCGTGGCGAGGCTGGGCGCAGAGAGGCTGGGGCTGCGGCCAGGCGTGGGGTGCG TTGGGAAGATGGCGTGGCGAGGCTGGGCGCAGGGAGGCTGGGGCTGCGGCCAGGCGTGGGGTGCG T C AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:183884721..183884876 26863196 MeRIP-seq:(Medium) rs1465150469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4732841,Human_RBP_ID_5120432,Human_RBP_ID_5325369,Human_RBP_ID_7167224,Human_RBP_ID_9334358,Human_RBP_ID_18424101,Human_RBP_ID_22455644,Human_RBP_ID_27841497 55624 RMVar_ID_55624 Human_SNP_ID_166314541 m1A Human chr3 + 183884831 183884831 183884831 CGCCTGGCCGCAGCCCCAGCCTCTCTGCGCCCAGCCTCGCCACGCCATCTTCCCAACCTCTGCCC CGCCTGGCCGCAGCCCCAGCCTCTCTGCGCCCCGCCTCGCCACGCCATCTTCCCAACCTCTGCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:183868001..183884900;chr3:183867952..183884900;chr3:183867951..183884900 26863196 MeRIP-seq:(Medium) rs755675651 Functional Loss SNV dbSNP153 33..33 33 - - - 55625 RMVar_ID_55625 Human_SNP_ID_166314542 m1A Human chr3 + 183884831 183884831 183884831 CGCCTGGCCGCAGCCCCAGCCTCTCTGCGCCCAGCCTCGCCACGCCATCTTCCCAACCTCTGCCC CGCCTGGCCGCAGCCCCAGCCTCTCTGCGCCCGGCCTCGCCACGCCATCTTCCCAACCTCTGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:183868001..183884900;chr3:183867952..183884900;chr3:183867951..183884900 26863196 MeRIP-seq:(Medium) rs755675651 Functional Loss SNV dbSNP153 33..33 33 - - - 55626 RMVar_ID_55626 Human_SNP_ID_166372566 m1A Human chr3 + 184116461 184116461 184116461 AAGAAAGAGTCCAATGACAAACCTGAAATTGAAGATGTTGGTTCTGATGAAGAAGAAGAAAAGAA AAGAAAGAGTCCAATGACAAACCTGAAATTGAGGATGTTGGTTCTGATGAAGAAGAAGAAAAGAA A G HSP90AA5P Ensembl:ENSG00000205955 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184116451..184116517 26863196 MeRIP-seq:(Medium) rs1430247629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17405352 55627 RMVar_ID_55627 Human_SNP_ID_166372571 m1A Human chr3 + 184116490 184116488 184116491 TGAAGATGTTGGTTCTGATGAAGAAGAAGAAAAGAAGGATGCTGACAAGAAGAAGAAGAAAAGTA TGAAGATGTTGGTTCTGATGAAGAAGAAGAA___AAGGATGCTGACAAGAAGAAGAAGAAAAGTA AAAG A HSP90AA5P Ensembl:ENSG00000205955 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184116427..184116511 26863196 MeRIP-seq:(Medium) rs569262057 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8264061 55628 RMVar_ID_55628 Human_SNP_ID_166377273 m1A Human chr3 - 184135554 184135554 184135554 GCTCACCCGAGGCTGGTCCTTGGAGATGGGGAAGAAGCGGCGATCGAAGCTATCGGCCACCAGAA GCTCACCCGAGGCTGGTCCTTGGAGATGGGGAGGAAGCGGCGATCGAAGCTATCGGCCACCAGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184135483..184135843 32194978 MeRIP-seq:(Medium) rs1439602258 Functional Loss SNV dbSNP153 33..33 33 - - - 55629 RMVar_ID_55629 Human_SNP_ID_166379224 m1A Human chr3 + 184142505 184142505 184142505 CCCTCTCTATAGATCATTGCCTTTTCCAGGTTACAATCCAGCAGAAGTAGGAGCTGCTGGCAAGG CCCTCTCTATAGATCATTGCCTTTTCCAGGTTGCAATCCAGCAGAAGTAGGAGCTGCTGGCAAGG A G EIF2B5 Ensembl:ENSG00000145191 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184142501..184142550 26863196 MeRIP-seq:(Medium) rs758301189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67883,Human_RBP_ID_26348558 Human_Splice_Rec_514688,Human_Splice_Rec_514689,Human_Splice_Rec_514718,Human_Splice_Rec_514719,Human_Splice_Rec_514748,Human_Splice_Rec_514749,Human_Splice_Rec_514776,Human_Splice_Rec_514777,Human_Splice_Rec_514806,Human_Splice_Rec_514807,Human_Splice_Rec_514836,Human_Splice_Rec_514837,Human_Splice_Rec_514866,Human_Splice_Rec_514867,Human_Splice_Rec_514896,Human_Splice_Rec_514897,Human_Splice_Rec_514924,Human_Splice_Rec_514925,Human_Splice_Rec_514954,Human_Splice_Rec_514955,Human_Splice_Rec_514984,Human_Splice_Rec_514985,Human_Splice_Rec_515012,Human_Splice_Rec_515013,Human_Splice_Rec_515042,Human_Splice_Rec_515043,Human_Splice_Rec_515066,Human_Splice_Rec_515067,Human_Splice_Rec_515090,Human_Splice_Rec_515091,Human_Splice_Rec_515106,Human_Splice_Rec_515107,Human_Splice_Rec_515124,Human_Splice_Rec_515125,Human_Splice_Rec_515150,Human_Splice_Rec_515151,Human_Splice_Rec_515188,Human_Splice_Rec_515189,Human_Splice_Rec_515216,Human_Splice_Rec_515217,Human_Splice_Rec_515252,Human_Splice_Rec_515253,Human_Splice_Rec_515280,Human_Splice_Rec_515281,Human_Splice_Rec_515302,Human_Splice_Rec_515303,Human_Splice_Rec_515322,Human_Splice_Rec_515323,Human_Splice_Rec_515348,Human_Splice_Rec_515349,Human_Splice_Rec_515364,Human_Splice_Rec_515365 Human_miRNA_ID_1999623,Human_miRNA_ID_2766482 RMVar_hsa_circ_21273,RMVar_hsa_circ_223287,RMVar_hsa_circ_73420,RMVar_hsa_circ_375025,RMVar_hsa_circ_16711,RMVar_hsa_circ_56215,RMVar_hsa_circ_267510,RMVar_hsa_circ_117000,RMVar_hsa_circ_81289,RMVar_hsa_circ_7189,RMVar_hsa_circ_223290,RMVar_hsa_circ_223291 55630 RMVar_ID_55630 Human_SNP_ID_166379314 m1A Human chr3 + 184142780 184142780 184142780 TTCTTTTTCCTCACCCATTATGGCTTCTCAGGACTCAAGATCAACATGGAAGAAGAGAGTGAAAG TTCTTTTTCCTCACCCATTATGGCTTCTCAGGGCTCAAGATCAACATGGAAGAAGAGAGTGAAAG A G EIF2B5 Ensembl:ENSG00000145191 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:184142776..184143105;chr3:184142776..184142825 26863196 MeRIP-seq:(Medium) rs753881395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936099,Human_RBP_ID_3964414,Human_RBP_ID_9349035,Human_RBP_ID_9394292,Human_RBP_ID_24547443,Human_RBP_ID_26347452,Human_RBP_ID_27822773 Human_Splice_Rec_514690,Human_Splice_Rec_514720,Human_Splice_Rec_514750,Human_Splice_Rec_514778,Human_Splice_Rec_514808,Human_Splice_Rec_514838,Human_Splice_Rec_514868,Human_Splice_Rec_514898,Human_Splice_Rec_514926,Human_Splice_Rec_514956,Human_Splice_Rec_514986,Human_Splice_Rec_515014,Human_Splice_Rec_515044,Human_Splice_Rec_515068,Human_Splice_Rec_515092,Human_Splice_Rec_515108,Human_Splice_Rec_515126,Human_Splice_Rec_515152,Human_Splice_Rec_515190,Human_Splice_Rec_515218,Human_Splice_Rec_515254,Human_Splice_Rec_515282,Human_Splice_Rec_515304,Human_Splice_Rec_515324,Human_Splice_Rec_515350,Human_Splice_Rec_515366 RMVar_hsa_circ_21273,RMVar_hsa_circ_223287,RMVar_hsa_circ_73420,RMVar_hsa_circ_375025,RMVar_hsa_circ_16711,RMVar_hsa_circ_56215,RMVar_hsa_circ_267510,RMVar_hsa_circ_117000,RMVar_hsa_circ_81289,RMVar_hsa_circ_223290,RMVar_hsa_circ_223291 55631 RMVar_ID_55631 Human_SNP_ID_166381073 m1A Human chr3 + 184149818 184149818 184149818 AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGATGCAAGTTACACCAACCAGGACAGAAATCATT AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGGTGCAAGTTACACCAACCAGGACAGAAATCATT A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1395674962 Functional Loss SNV dbSNP153 33..33 33 - - - 55632 RMVar_ID_55632 Human_SNP_ID_166382612 m1A Human chr3 + 184155402 184155402 184155402 AAGCCCTGGGCCGGGAGGGCCGCGGCCACCGGAAGAGTCGCGGTCGCCAGTCCAGTCGGGAGAGT AAGCCCTGGGCCGGGAGGGCCGCGGCCACCGGGAGAGTCGCGGTCGCCAGTCCAGTCGGGAGAGT A G DVL3 Ensembl:ENSG00000161202 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184155351..184155675 26863196 MeRIP-seq:(Medium) rs904442086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757590 55633 RMVar_ID_55633 Human_SNP_ID_166382613 m1A Human chr3 + 184155403 184155403 184155403 AGCCCTGGGCCGGGAGGGCCGCGGCCACCGGAAGAGTCGCGGTCGCCAGTCCAGTCGGGAGAGTG AGCCCTGGGCCGGGAGGGCCGCGGCCACCGGAGGAGTCGCGGTCGCCAGTCCAGTCGGGAGAGTG A G DVL3 Ensembl:ENSG00000161202 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184155326..184155725 26863196 MeRIP-seq:(Medium) rs998704462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757590,Human_RBP_ID_17671337 55634 RMVar_ID_55634 Human_SNP_ID_166382651 m1A Human chr3 - 184155532 184155532 184155532 GCGGCGCGCGGCGCGGCCCAGCGGCTCAACCCAGCTCGGCGGCTGCTGGCGGCGCCAGCTCCCTT GCGGCGCGCGGCGCGGCCCAGCGGCTCAACCCTGCTCGGCGGCTGCTGGCGGCGCCAGCTCCCTT T A - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:184155437..184155538 26863410 MeRIP-seq:(Medium) rs1387267664 Functional Loss SNV dbSNP153 33..33 33 - - - 55635 RMVar_ID_55635 Human_SNP_ID_166385134 m1A Human chr3 - 184165194 184165194 184165194 TAGCCTCCCAGACCCCATACCCGCTCAATCCGAGAAACCTTCTGCTTCCGCCGCCGCCGCTTGTG TAGCCTCCCAGACCCCATACCCGCTCAATCCGGGAAACCTTCTGCTTCCGCCGCCGCCGCTTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184165092..184165236 26863196 MeRIP-seq:(Medium) rs9879096 Functional Loss SNV dbSNP153 33..33 33 - - - 55636 RMVar_ID_55636 Human_SNP_ID_166385135 m1A Human chr3 - 184165194 184165194 184165194 TAGCCTCCCAGACCCCATACCCGCTCAATCCGAGAAACCTTCTGCTTCCGCCGCCGCCGCTTGTG TAGCCTCCCAGACCCCATACCCGCTCAATCCGCGAAACCTTCTGCTTCCGCCGCCGCCGCTTGTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184165092..184165236 26863196 MeRIP-seq:(Medium) rs9879096 Functional Loss SNV dbSNP153 33..33 33 - - - 55637 RMVar_ID_55637 Human_SNP_ID_166385523 m1A Human chr3 - 184166524 184166524 184166524 AAGCCCCTTGCCCAGTGCCCCATTCCATCCATACCCCGGTTTGTGCACAATCTCCCGCAGTACCC AAGCCCCTTGCCCAGTGCCCCATTCCATCCATTCCCCGGTTTGTGCACAATCTCCCGCAGTACCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184166515..184166616 32194978 MeRIP-seq:(Medium) rs1318753006 Functional Loss SNV dbSNP153 33..33 33 - - - 55638 RMVar_ID_55638 Human_SNP_ID_166385653 m1A Human chr3 + 184166927 184166927 184166927 CTGCATACGGCATGAGCCCCTCCCTGAGCACCATCACCTCCACCAGCTCCTCCATCACCAGTTCC CTGCATACGGCATGAGCCCCTCCCTGAGCACCGTCACCTCCACCAGCTCCTCCATCACCAGTTCC A G DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184166876..184166950 26863196 MeRIP-seq:(Medium) rs1315575405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596410,Human_RBP_ID_4733023,Human_RBP_ID_26824258,Human_RBP_ID_27049556 Human_Splice_Rec_515387,Human_Splice_Rec_515430,Human_Splice_Rec_515431,Human_Splice_Rec_515477,Human_Splice_Rec_515497,Human_Splice_Rec_515511 Human_miRNA_ID_273403,Human_miRNA_ID_847532,Human_miRNA_ID_2050785,Human_miRNA_ID_2291338,Human_miRNA_ID_2356683,Human_miRNA_ID_3059128 RMVar_hsa_circ_72711,RMVar_hsa_circ_331627,RMVar_hsa_circ_76189,RMVar_hsa_circ_223296,RMVar_hsa_circ_65560,RMVar_hsa_circ_8367 55639 RMVar_ID_55639 Human_SNP_ID_166386550 m1A Human chr3 + 184170133 184170133 184170133 TGGCCCATGGCTTTCCCGTACCAGTACCCGCCACCCCCGCACCCATACAACCCGCACCCGGGCTT TGGCCCATGGCTTTCCCGTACCAGTACCCGCCGCCCCCGCACCCATACAACCCGCACCCGGGCTT A G DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184170088..184170218 26863196 MeRIP-seq:(Medium) rs1335339989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17404788,Human_RBP_ID_18194739,Human_RBP_ID_18446321 Human_Splice_Rec_515393,Human_Splice_Rec_515437,Human_Splice_Rec_515483,Human_Splice_Rec_515517 55640 RMVar_ID_55640 Human_SNP_ID_166386716 m1A Human chr3 + 184170426 184170426 184170426 AGTCCGGGGGCAGCGGCAGCGAATCGGACCACACCACACGCAGCAGCCTGCGGGGGCCGCGGGAG AGTCCGGGGGCAGCGGCAGCGAATCGGACCACGCCACACGCAGCAGCCTGCGGGGGCCGCGGGAG A G DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184170376..184170796 26863196 MeRIP-seq:(Medium) rs1489880646 Functional Loss SNV dbSNP153 33..33 33 - - - 55641 RMVar_ID_55641 Human_SNP_ID_166386864 m1A Human chr3 + 184170711 184170711 184170711 CGGAACTGACCGCCAGCAGACAGTCCTTCCGCATGGCCATGGGAAACCCCAGTGAGTTCTTTGTG CGGAACTGACCGCCAGCAGACAGTCCTTCCGCCTGGCCATGGGAAACCCCAGTGAGTTCTTTGTG A C DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184170660..184170784 26863196 MeRIP-seq:(Medium) rs775113252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032205 55642 RMVar_ID_55642 Human_SNP_ID_166386865 m1A Human chr3 + 184170711 184170711 184170711 CGGAACTGACCGCCAGCAGACAGTCCTTCCGCATGGCCATGGGAAACCCCAGTGAGTTCTTTGTG CGGAACTGACCGCCAGCAGACAGTCCTTCCGCGTGGCCATGGGAAACCCCAGTGAGTTCTTTGTG A G DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184170660..184170784 26863196 MeRIP-seq:(Medium) rs775113252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032205 55643 RMVar_ID_55643 Human_SNP_ID_166388005 m1A Human chr3 + 184174941 184174941 184174941 TGGGATCCGGAGAGTGGCCGGGCCGGCAGAGCAGGGGGCCGAGGACACCAGGTGAGCCGGGGATC TGGGATCCGGAGAGTGGCCGGGCCGGCAGAGCGGGGGGCCGAGGACACCAGGTGAGCCGGGGATC A G AP2M1 Ensembl:ENSG00000161203 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:184174876..184175009 26863196 MeRIP-seq:(Medium) rs970486883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247507,Human_RBP_ID_783589,Human_RBP_ID_836090,Human_RBP_ID_938412,Human_RBP_ID_3964435,Human_RBP_ID_4757591,Human_RBP_ID_5120624,Human_RBP_ID_5325373,Human_RBP_ID_5530728,Human_RBP_ID_9334364,Human_RBP_ID_18424362,Human_RBP_ID_22455646 Human_Splice_Rec_515521,Human_Splice_Rec_515541,Human_Splice_Rec_515545,Human_Splice_Rec_515551,Human_Splice_Rec_515557,Human_Splice_Rec_515583,Human_Splice_Rec_515605,Human_Splice_Rec_515617,Human_Splice_Rec_515621 Human_miRNA_ID_2394628,Human_miRNA_ID_2906665,Human_miRNA_ID_3025496 RMVar_hsa_circ_91772,RMVar_hsa_circ_107035,RMVar_hsa_circ_123752,RMVar_hsa_circ_223301,RMVar_hsa_circ_223302,RMVar_hsa_circ_223303,RMVar_hsa_circ_223304 55644 RMVar_ID_55644 Human_SNP_ID_166388519 m1A Human chr3 + 184177002 184177002 184177002 GGCCGCGGAGACTGATCTGCCGCCATGATTGGAGGCTTATTCATCTATAATCACAAGGGGGAGGT GGCCGCGGAGACTGATCTGCCGCCATGATTGGTGGCTTATTCATCTATAATCACAAGGGGGAGGT A T AP2M1 Ensembl:ENSG00000161203 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr3:184176918..184177075;chr3:184176951..184177025 26863196 MeRIP-seq:(Medium) rs1396107492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247508,Human_RBP_ID_934053,Human_RBP_ID_1032211,Human_RBP_ID_1385119,Human_RBP_ID_1623205,Human_RBP_ID_1957378,Human_RBP_ID_3964436,Human_RBP_ID_4757592,Human_RBP_ID_5120434,Human_RBP_ID_7167562,Human_RBP_ID_8122327,Human_RBP_ID_8566950,Human_RBP_ID_9147759,Human_RBP_ID_9260958,Human_RBP_ID_14744852,Human_RBP_ID_17402729,Human_RBP_ID_17518741,Human_RBP_ID_17661590,Human_RBP_ID_18001140,Human_RBP_ID_18194741,Human_RBP_ID_22457081,Human_RBP_ID_22509192,Human_RBP_ID_22822821,Human_RBP_ID_23288315,Human_RBP_ID_26824260,Human_RBP_ID_27159744,Human_RBP_ID_27716009 Human_Splice_Rec_515522,Human_Splice_Rec_515523,Human_Splice_Rec_515542,Human_Splice_Rec_515543,Human_Splice_Rec_515546,Human_Splice_Rec_515547,Human_Splice_Rec_515552,Human_Splice_Rec_515553,Human_Splice_Rec_515558,Human_Splice_Rec_515559,Human_Splice_Rec_515584,Human_Splice_Rec_515585,Human_Splice_Rec_515606,Human_Splice_Rec_515607,Human_Splice_Rec_515618,Human_Splice_Rec_515619,Human_Splice_Rec_515622,Human_Splice_Rec_515623,Human_Splice_Rec_515628,Human_Splice_Rec_515629,Human_Splice_Rec_515631,Human_Splice_Rec_515649,Human_Splice_Rec_515663,Human_Splice_Rec_515671,Human_Splice_Rec_515679 RMVar_hsa_circ_103137,RMVar_hsa_circ_91772,RMVar_hsa_circ_107035,RMVar_hsa_circ_123752,RMVar_hsa_circ_223301,RMVar_hsa_circ_223302,RMVar_hsa_circ_223303,RMVar_hsa_circ_119742,RMVar_hsa_circ_223304,RMVar_hsa_circ_223305,RMVar_hsa_circ_223306 55645 RMVar_ID_55645 Human_SNP_ID_166388536 m1A Human chr3 - 184177069 184177069 184177069 GGTGGGGCACAGCTGGCTCCGCCAGGGGACTCACCCGATGTCATCTCGGTAGACTCGGGAGATGA GGTGGGGCACAGCTGGCTCCGCCAGGGGACTCTCCCGATGTCATCTCGGTAGACTCGGGAGATGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:184176949..184177574 32194978 MeRIP-seq:(Medium) rs113086272 Functional Loss SNV dbSNP153 33..33 33 - - - 55646 RMVar_ID_55646 Human_SNP_ID_166388537 m1A Human chr3 - 184177069 184177069 184177069 GGTGGGGCACAGCTGGCTCCGCCAGGGGACTCACCCGATGTCATCTCGGTAGACTCGGGAGATGA GGTGGGGCACAGCTGGCTCCGCCAGGGGACTCCCCCGATGTCATCTCGGTAGACTCGGGAGATGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:184176949..184177574 32194978 MeRIP-seq:(Medium) rs113086272 Functional Loss SNV dbSNP153 33..33 33 - - - 55647 RMVar_ID_55647 Human_SNP_ID_166389033 m1A Human chr3 + 184178855 184178855 184178855 TGCTGAGCAGGCCCTATGCACTCTTTTCCCTCAGGAGGAACGCAGTGGATGCCTTTCGGGTCAAT TGCTGAGCAGGCCCTATGCACTCTTTTCCCTCGGGAGGAACGCAGTGGATGCCTTTCGGGTCAAT A G AP2M1 Ensembl:ENSG00000161203 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184178851..184179000 32194978 MeRIP-seq:(Medium) rs112256941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68157,Human_RBP_ID_4757594 RMVar_hsa_circ_103137,RMVar_hsa_circ_107035,RMVar_hsa_circ_123752,RMVar_hsa_circ_223302,RMVar_hsa_circ_223303,RMVar_hsa_circ_119742,RMVar_hsa_circ_223304,RMVar_hsa_circ_268836,RMVar_hsa_circ_223305,RMVar_hsa_circ_223306,RMVar_hsa_circ_318513,RMVar_hsa_circ_346344,RMVar_hsa_circ_40168,RMVar_hsa_circ_113066 55648 RMVar_ID_55648 Human_SNP_ID_166389608 m1A Human chr3 + 184180910 184180905 184180910 CCAGGTAACTGGGCAGATTGGCTGGCGGCGAGAGGGTATCAAGTATCGTCGGAATGAGCTCTTCC CCAGGTAACTGGGCAGATTGGCTGGCGG_____GGGTATCAAGTATCGTCGGAATGAGCTCTTCC GCGAGA G AP2M1 Ensembl:ENSG00000161203 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1356228837 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_247509,Human_RBP_ID_596470,Human_RBP_ID_8566962,Human_RBP_ID_14744882,Human_RBP_ID_18013020,Human_RBP_ID_22509195,Human_RBP_ID_23989107,Human_RBP_ID_27841503 Human_Splice_Rec_515528,Human_Splice_Rec_515529,Human_Splice_Rec_515570,Human_Splice_Rec_515571,Human_Splice_Rec_515592,Human_Splice_Rec_515593,Human_Splice_Rec_515616,Human_Splice_Rec_515636,Human_Splice_Rec_515637,Human_Splice_Rec_515656,Human_Splice_Rec_515670,Human_Splice_Rec_515678,Human_Splice_Rec_515684,Human_Splice_Rec_515685,Human_Splice_Rec_515700,Human_Splice_Rec_515701,Human_Splice_Rec_515706,Human_Splice_Rec_515707,Human_Splice_Rec_515710,Human_Splice_Rec_515711 RMVar_hsa_circ_103137,RMVar_hsa_circ_107035,RMVar_hsa_circ_123752,RMVar_hsa_circ_223302,RMVar_hsa_circ_223303,RMVar_hsa_circ_119742,RMVar_hsa_circ_20167,RMVar_hsa_circ_268836,RMVar_hsa_circ_223305,RMVar_hsa_circ_223306,RMVar_hsa_circ_113066,RMVar_hsa_circ_223308,RMVar_hsa_circ_79173,RMVar_hsa_circ_223310,RMVar_hsa_circ_223311 55649 RMVar_ID_55649 Human_SNP_ID_166389864 m1A Human chr3 - 184181950 184181950 184181950 TGGTGCGTCCCACTTCTCGCACTAGCGGGATCACCCGGAAGGGAAGGATGATGTCCTTGGTTGTG TGGTGCGTCCCACTTCTCGCACTAGCGGGATCGCCCGGAAGGGAAGGATGATGTCCTTGGTTGTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184181749..184181949 32194978 MeRIP-seq:(Medium) rs757608518 Functional Loss SNV dbSNP153 33..33 33 - - - 55650 RMVar_ID_55650 Human_SNP_ID_166390288 m1A Human chr3 - 184183499 184183499 184183499 TCAAACACCTTCAAGTAGCGCACCTTGAGGCCAGAGGGCGCGAATGGCACCTGGGCAAGGAGAGC TCAAACACCTTCAAGTAGCGCACCTTGAGGCCCGAGGGCGCGAATGGCACCTGGGCAAGGAGAGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184183476..184183800 32194978 MeRIP-seq:(Medium) rs749297458 Functional Loss SNV dbSNP153 33..33 33 - - - 55651 RMVar_ID_55651 Human_SNP_ID_166390305 m1A Human chr3 + 184183650 184183634 184183650 TGCCACTAGGCAGCTAGCCCACCTCCCCAGCCACCCTCCTCCACAGGTCCAGGTGCCGCTCCCTC TGCCACTAGGCAGCTAG________________CCCTCCTCCACAGGTCCAGGTGCCGCTCCCTC GCCCACCTCCCCAGCCA G AP2M1 Ensembl:ENSG00000161203 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184183600..184183742 26863196 MeRIP-seq:(Medium) rs1366079664 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_247511,Human_RBP_ID_596498,Human_RBP_ID_17289342,Human_RBP_ID_17402734,Human_RBP_ID_18194748,Human_RBP_ID_18954744,Human_RBP_ID_27315987 Human_miRNA_ID_2508752 RMVar_hsa_circ_103137,RMVar_hsa_circ_123752,RMVar_hsa_circ_223303,RMVar_hsa_circ_223306,RMVar_hsa_circ_79173,RMVar_hsa_circ_85009,RMVar_hsa_circ_223311,RMVar_hsa_circ_223313,RMVar_hsa_circ_101386,RMVar_hsa_circ_119948,RMVar_hsa_circ_223314,RMVar_hsa_circ_122077,RMVar_hsa_circ_91463,RMVar_hsa_circ_110951,RMVar_hsa_circ_223315,RMVar_hsa_circ_223316,RMVar_hsa_circ_223318,RMVar_hsa_circ_223319 55652 RMVar_ID_55652 Human_SNP_ID_166390391 m1A Human chr3 + 184183976 184183976 184183976 GTTGGTTGCCCCTCACCTCAGAGCTCCCCCAAAGGCCAGTAATGGATCCCCGGCCTCAGTCCCTA GTTGGTTGCCCCTCACCTCAGAGCTCCCCCAAGGGCCAGTAATGGATCCCCGGCCTCAGTCCCTA A G AP2M1 Ensembl:ENSG00000161203 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184183925..184184022 26863196 MeRIP-seq:(Medium) rs1296826304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596508,Human_RBP_ID_783599,Human_RBP_ID_1623263,Human_RBP_ID_1957417,Human_RBP_ID_3699219,Human_RBP_ID_4763166,Human_RBP_ID_8566992,Human_RBP_ID_17088726,Human_RBP_ID_17661594,Human_RBP_ID_18001155,Human_RBP_ID_18194964,Human_RBP_ID_18803615,Human_RBP_ID_18954748 Human_miRNA_ID_2155200,Human_miRNA_ID_2158764,Human_miRNA_ID_3095598 RMVar_hsa_circ_103137,RMVar_hsa_circ_123752,RMVar_hsa_circ_223303,RMVar_hsa_circ_223306,RMVar_hsa_circ_79173,RMVar_hsa_circ_85009,RMVar_hsa_circ_223311,RMVar_hsa_circ_223313,RMVar_hsa_circ_101386,RMVar_hsa_circ_119948,RMVar_hsa_circ_223314,RMVar_hsa_circ_122077,RMVar_hsa_circ_91463,RMVar_hsa_circ_110951,RMVar_hsa_circ_223315,RMVar_hsa_circ_223316,RMVar_hsa_circ_223318,RMVar_hsa_circ_223319 55653 RMVar_ID_55653 Human_SNP_ID_166390407 m1A Human chr3 - 184184025 184184025 184184025 ACGAAGTCACACGTGTACAAAATGAAGCTCACACTATCCCAAAGCAGAGTAGGGACTGAGGCCGG ACGAAGTCACACGTGTACAAAATGAAGCTCACGCTATCCCAAAGCAGAGTAGGGACTGAGGCCGG T C HSALNG0031211 RNACentral:URS0000EA6DF1 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:184184001..184184025 26863196 MeRIP-seq:(Medium) rs1265881669 Functional Loss SNV dbSNP153 33..33 33 - - - 55654 RMVar_ID_55654 Human_SNP_ID_166391259 m1A Human chr3 - 184186555 184186555 184186555 ACACCTCTTGCAATAGTTCCCCTACAGCTTCCACCAGGTCATCCACAGACTCGAAGTCCGCGCTG ACACCTCTTGCAATAGTTCCCCTACAGCTTCCTCCAGGTCATCCACAGACTCGAAGTCCGCGCTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184186497..184186610 26863196 MeRIP-seq:(Medium) rs1316300769 Functional Loss SNV dbSNP153 33..33 33 - - - 55655 RMVar_ID_55655 Human_SNP_ID_166391371 m1A Human chr3 - 184186799 184186799 184186799 AGCACCTGGCTATTTCCCTGGCTTTGTGGCTCAGCCCTATGTGGGTAGGGATAGAAAGCGCAGAG AGCACCTGGCTATTTCCCTGGCTTTGTGGCTCGGCCCTATGTGGGTAGGGATAGAAAGCGCAGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184186793..184186894 32194978 MeRIP-seq:(Medium) rs1268545836 Functional Loss SNV dbSNP153 33..33 33 - - - 55656 RMVar_ID_55656 Human_SNP_ID_166407401 m1A Human chr3 - 184242885 184242885 184242885 CTGCTTCAGCCGCTCCCTCCACTACCAGTTCTACGTCTGGTATTTCCACACACTGCCCTACCTCC CTGCTTCAGCCGCTCCCTCCACTACCAGTTCTGCGTCTGGTATTTCCACACACTGCCCTACCTCC T C ALG3 Ensembl:ENSG00000214160 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs747389321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17289353,Human_RBP_ID_17404799,Human_RBP_ID_17518757,Human_RBP_ID_18954754,Human_RBP_ID_22455652,Human_RBP_ID_23989185,Human_RBP_ID_24497016 Human_Splice_Rec_516093,Human_Splice_Rec_516107,Human_Splice_Rec_516121,Human_Splice_Rec_516123,Human_Splice_Rec_516137,Human_Splice_Rec_516147 Human_miRNA_ID_1013275,Human_miRNA_ID_1021432,Human_miRNA_ID_1295276,Human_miRNA_ID_1299233,Human_miRNA_ID_1373543,Human_miRNA_ID_1989387,Human_miRNA_ID_1989388,Human_miRNA_ID_2461493,Human_miRNA_ID_2461494 RMVar_hsa_circ_123499,RMVar_hsa_circ_113749,RMVar_hsa_circ_223334,RMVar_hsa_circ_223335 55657 RMVar_ID_55657 Human_SNP_ID_166407402 m1A Human chr3 - 184242885 184242885 184242885 CTGCTTCAGCCGCTCCCTCCACTACCAGTTCTACGTCTGGTATTTCCACACACTGCCCTACCTCC CTGCTTCAGCCGCTCCCTCCACTACCAGTTCTCCGTCTGGTATTTCCACACACTGCCCTACCTCC T G ALG3 Ensembl:ENSG00000214160 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs747389321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17289353,Human_RBP_ID_17404799,Human_RBP_ID_17518757,Human_RBP_ID_18954754,Human_RBP_ID_22455652,Human_RBP_ID_23989185,Human_RBP_ID_24497016 Human_Splice_Rec_516093,Human_Splice_Rec_516107,Human_Splice_Rec_516121,Human_Splice_Rec_516123,Human_Splice_Rec_516137,Human_Splice_Rec_516147 Human_miRNA_ID_1013275,Human_miRNA_ID_1021432,Human_miRNA_ID_1295276,Human_miRNA_ID_1299233,Human_miRNA_ID_1373543,Human_miRNA_ID_1989387,Human_miRNA_ID_1989388,Human_miRNA_ID_2461493,Human_miRNA_ID_2461494 RMVar_hsa_circ_123499,RMVar_hsa_circ_113749,RMVar_hsa_circ_223334,RMVar_hsa_circ_223335 55658 RMVar_ID_55658 Human_SNP_ID_166407667 m1A Human chr3 - 184243833 184243831 184243833 TCGAGCCTTCCACCTGGCCCTGTTGACTGCCCACCTCACCCTGCTCCTGCTGTTTGCCCTCTGCA TCGAGCCTTCCACCTGGCCCTGTTGACTGCCC__CTCACCCTGCTCCTGCTGTTTGCCCTCTGCA GGT G ALG3 Ensembl:ENSG00000214160 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184243623..184244364 32194978 MeRIP-seq:(Medium) rs765684289 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4733255,Human_RBP_ID_17292857,Human_RBP_ID_17404800,Human_RBP_ID_18001191,Human_RBP_ID_18209820,Human_RBP_ID_18803648,Human_RBP_ID_22278658,Human_RBP_ID_22770083,Human_RBP_ID_26824283,Human_RBP_ID_27500197 Human_Splice_Rec_516091,Human_Splice_Rec_516105,Human_Splice_Rec_516119,Human_Splice_Rec_516135,Human_Splice_Rec_516145,Human_Splice_Rec_516155,Human_Splice_Rec_516157,Human_Splice_Rec_516163 Human_miRNA_ID_169007,Human_miRNA_ID_601503,Human_miRNA_ID_1047438,Human_miRNA_ID_1373544,Human_miRNA_ID_2006475,Human_miRNA_ID_2006476,Human_miRNA_ID_2220257,Human_miRNA_ID_2220258,Human_miRNA_ID_2483300,Human_miRNA_ID_2483301,Human_miRNA_ID_2872723,Human_miRNA_ID_2872724,Human_miRNA_ID_2980689,Human_miRNA_ID_2980690,Human_miRNA_ID_3071677,Human_miRNA_ID_3071678 RMVar_hsa_circ_91229,RMVar_hsa_circ_123499,RMVar_hsa_circ_113749,RMVar_hsa_circ_223334,RMVar_hsa_circ_223335,RMVar_hsa_circ_337974,RMVar_hsa_circ_223336 55659 RMVar_ID_55659 Human_SNP_ID_166407670 m1A Human chr3 - 184243833 184243833 184243833 TCGAGCCTTCCACCTGGCCCTGTTGACTGCCCACCTCACCCTGCTCCTGCTGTTTGCCCTCTGCA TCGAGCCTTCCACCTGGCCCTGTTGACTGCCCGCCTCACCCTGCTCCTGCTGTTTGCCCTCTGCA T C ALG3 Ensembl:ENSG00000214160 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184243623..184244364 32194978 MeRIP-seq:(Medium) rs557190648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4733255,Human_RBP_ID_17292857,Human_RBP_ID_17404800,Human_RBP_ID_18001191,Human_RBP_ID_18209820,Human_RBP_ID_18803648,Human_RBP_ID_22278658,Human_RBP_ID_22770083,Human_RBP_ID_26824283,Human_RBP_ID_27500197 Human_Splice_Rec_516091,Human_Splice_Rec_516105,Human_Splice_Rec_516119,Human_Splice_Rec_516135,Human_Splice_Rec_516145,Human_Splice_Rec_516155,Human_Splice_Rec_516157,Human_Splice_Rec_516163 Human_miRNA_ID_169007,Human_miRNA_ID_601503,Human_miRNA_ID_1047438,Human_miRNA_ID_1373544,Human_miRNA_ID_2006475,Human_miRNA_ID_2006476,Human_miRNA_ID_2220257,Human_miRNA_ID_2220258,Human_miRNA_ID_2483300,Human_miRNA_ID_2483301,Human_miRNA_ID_2872723,Human_miRNA_ID_2872724,Human_miRNA_ID_2980689,Human_miRNA_ID_2980690,Human_miRNA_ID_3071677,Human_miRNA_ID_3071678 RMVar_hsa_circ_91229,RMVar_hsa_circ_123499,RMVar_hsa_circ_113749,RMVar_hsa_circ_223334,RMVar_hsa_circ_223335,RMVar_hsa_circ_337974,RMVar_hsa_circ_223336 55660 RMVar_ID_55660 Human_SNP_ID_166407671 m1A Human chr3 - 184243833 184243833 184243833 TCGAGCCTTCCACCTGGCCCTGTTGACTGCCCACCTCACCCTGCTCCTGCTGTTTGCCCTCTGCA TCGAGCCTTCCACCTGGCCCTGTTGACTGCCCCCCTCACCCTGCTCCTGCTGTTTGCCCTCTGCA T G ALG3 Ensembl:ENSG00000214160 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184243623..184244364 32194978 MeRIP-seq:(Medium) rs557190648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4733255,Human_RBP_ID_17292857,Human_RBP_ID_17404800,Human_RBP_ID_18001191,Human_RBP_ID_18209820,Human_RBP_ID_18803648,Human_RBP_ID_22278658,Human_RBP_ID_22770083,Human_RBP_ID_26824283,Human_RBP_ID_27500197 Human_Splice_Rec_516091,Human_Splice_Rec_516105,Human_Splice_Rec_516119,Human_Splice_Rec_516135,Human_Splice_Rec_516145,Human_Splice_Rec_516155,Human_Splice_Rec_516157,Human_Splice_Rec_516163 Human_miRNA_ID_169007,Human_miRNA_ID_601503,Human_miRNA_ID_1047438,Human_miRNA_ID_1373544,Human_miRNA_ID_2006475,Human_miRNA_ID_2006476,Human_miRNA_ID_2220257,Human_miRNA_ID_2220258,Human_miRNA_ID_2483300,Human_miRNA_ID_2483301,Human_miRNA_ID_2872723,Human_miRNA_ID_2872724,Human_miRNA_ID_2980689,Human_miRNA_ID_2980690,Human_miRNA_ID_3071677,Human_miRNA_ID_3071678 RMVar_hsa_circ_91229,RMVar_hsa_circ_123499,RMVar_hsa_circ_113749,RMVar_hsa_circ_223334,RMVar_hsa_circ_223335,RMVar_hsa_circ_337974,RMVar_hsa_circ_223336 55661 RMVar_ID_55661 Human_SNP_ID_166409618 m1A Human chr3 - 184249770 184249770 184249770 AGAATCGGCTGCGCCTTGGTAGCGCTGATCCCAGTACTCGACTTCGCGGTACCCGCAGTTCCGCT AGAATCGGCTGCGCCTTGGTAGCGCTGATCCCGGTACTCGACTTCGCGGTACCCGCAGTTCCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184249720..184249849 26863196 MeRIP-seq:(Medium) rs764759339 Functional Loss SNV dbSNP153 33..33 33 - - - 55662 RMVar_ID_55662 Human_SNP_ID_166412302 m1A Human chr3 - 184259947 184259947 184259947 GGCCGCGGTAGCGGCGGCGCGGACCCGCCCGGAACCCGCCGCCGCGCTCATGCACTTTAAAACCT GGCCGCGGTAGCGGCGGCGCGGACCCGCCCGGGACCCGCCGCCGCGCTCATGCACTTTAAAACCT T C CAMK2N2 Ensembl:ENSG00000163888 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184259896..184259980 26863196 MeRIP-seq:(Medium) rs1458255647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97225,RMVar_hsa_circ_223343 55663 RMVar_ID_55663 Human_SNP_ID_166412430 m1A Human chr3 - 184260248 184260248 184260248 CATCGCCGCCGCCCCCCGAGGCCGCGCGGCTGACGCGCTTTCTCCCTGCGCAGTGGTGATCGAGG CATCGCCGCCGCCCCCCGAGGCCGCGCGGCTGGCGCGCTTTCTCCCTGCGCAGTGGTGATCGAGG T C CAMK2N2 Ensembl:ENSG00000163888 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184260243..184260823 26863196 MeRIP-seq:(Medium) rs1363278155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97225,RMVar_hsa_circ_223343 55664 RMVar_ID_55664 Human_SNP_ID_166412780 m1A Human chr3 - 184261299 184261299 184261299 CCCCGCCGCAGTCCCGCTCCCGCCCCGCGCCCACCCCGCGCCCGCCATGTCCGAGATCCTGCCCT CCCCGCCGCAGTCCCGCTCCCGCCCCGCGCCCGCCCCGCGCCCGCCATGTCCGAGATCCTGCCCT T C CAMK2N2 Ensembl:ENSG00000163888 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:184261251..184261475 26863196 MeRIP-seq:(Medium) rs751744923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97225,RMVar_hsa_circ_223343 55665 RMVar_ID_55665 Human_SNP_ID_166412781 m1A Human chr3 - 184261299 184261299 184261299 CCCCGCCGCAGTCCCGCTCCCGCCCCGCGCCCACCCCGCGCCCGCCATGTCCGAGATCCTGCCCT CCCCGCCGCAGTCCCGCTCCCGCCCCGCGCCCCCCCCGCGCCCGCCATGTCCGAGATCCTGCCCT T G CAMK2N2 Ensembl:ENSG00000163888 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:184261251..184261475 26863196 MeRIP-seq:(Medium) rs751744923 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_97225,RMVar_hsa_circ_223343 55666 RMVar_ID_55666 Human_SNP_ID_166423366 m1A Human chr3 + 184299289 184299289 184299289 GGCGGCGGAGATGGAGGAGGGAGGCCGGGACAAGGCGCCGGTGCAGCCCCAGCAGTCTCCAGCGG GGCGGCGGAGATGGAGGAGGGAGGCCGGGACAGGGCGCCGGTGCAGCCCCAGCAGTCTCCAGCGG A G PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184299192..184299456 26863196 MeRIP-seq:(Medium) rs1288082425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70316,Human_RBP_ID_248575,Human_RBP_ID_784772,Human_RBP_ID_4733336,Human_RBP_ID_5325375,Human_RBP_ID_8875683,Human_RBP_ID_9302562,Human_RBP_ID_22092036,Human_RBP_ID_22457089,Human_RBP_ID_26347470,Human_RBP_ID_27823785 55667 RMVar_ID_55667 Human_SNP_ID_166423394 m1A Human chr3 + 184299351 184299351 184299351 CGGCGGCCCCCGGCGGCACGGACGAGAAGCCGAGCGGCAAGGAGCGGCGGGATGCCGGGGACAAG CGGCGGCCCCCGGCGGCACGGACGAGAAGCCGGGCGGCAAGGAGCGGCGGGATGCCGGGGACAAG A G PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr3:184299251..184299400;chr3:184299251..184299425 26863410 MeRIP-seq:(Medium) rs1305715113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70316,Human_RBP_ID_4757600,Human_RBP_ID_5325375,Human_RBP_ID_8875216,Human_RBP_ID_9302562,Human_RBP_ID_22092037,Human_RBP_ID_26347470,Human_RBP_ID_27823785 Human_Splice_Rec_516443,Human_Splice_Rec_516453,Human_Splice_Rec_516461,Human_Splice_Rec_516467,Human_Splice_Rec_516507 55668 RMVar_ID_55668 Human_SNP_ID_166423547 m1A Human chr3 - 184299862 184299862 184299862 ACGAGCATCTCCAGTTCATCTTGAAGCTGTTTATCCTCTTCAGACTGGAGGGTTGGGAGAAGCAG ACGAGCATCTCCAGTTCATCTTGAAGCTGTTTTTCCTCTTCAGACTGGAGGGTTGGGAGAAGCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184299848..184300450 26863196 MeRIP-seq:(Medium) rs1206952258 Functional Loss SNV dbSNP153 33..33 33 - - - 55669 RMVar_ID_55669 Human_SNP_ID_166423548 m1A Human chr3 + 184299864 184299864 184299864 GCTTCTCCCAACCCTCCAGTCTGAAGAGGATAAACAGCTTCAAGATGAACTGGAGATGCTCGTGG GCTTCTCCCAACCCTCCAGTCTGAAGAGGATAGACAGCTTCAAGATGAACTGGAGATGCTCGTGG A G PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184299851..184299925 26863196 MeRIP-seq:(Medium) rs1326847050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1957440,Human_RBP_ID_3699262,Human_RBP_ID_4758969,Human_RBP_ID_9302563,Human_RBP_ID_9394311,Human_RBP_ID_19118964,Human_RBP_ID_23115914,Human_RBP_ID_26348571 Human_Splice_Rec_516444,Human_Splice_Rec_516445,Human_Splice_Rec_516454,Human_Splice_Rec_516455,Human_Splice_Rec_516462,Human_Splice_Rec_516463,Human_Splice_Rec_516468,Human_Splice_Rec_516469,Human_Splice_Rec_516508,Human_Splice_Rec_516509,Human_Splice_Rec_516512,Human_Splice_Rec_516513,Human_Splice_Rec_516519,Human_Splice_Rec_516521 Human_miRNA_ID_1542917,Human_miRNA_ID_1564368,Human_miRNA_ID_1596004,Human_miRNA_ID_2069697,Human_miRNA_ID_2802597 RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_20912 55670 RMVar_ID_55670 Human_SNP_ID_166423671 m1A Human chr3 + 184300289 184300289 184300289 GAGCCCTGTCGTCTCTTGATCAGGAGAAGGATACATCCCTGTATCGACCAGCGCTGGAGGAATTG GAGCCCTGTCGTCTCTTGATCAGGAGAAGGATTCATCCCTGTATCGACCAGCGCTGGAGGAATTG A T PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184300276..184300325 26863196 MeRIP-seq:(Medium) rs1172961641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_938095,Human_RBP_ID_1957442,Human_RBP_ID_4733345,Human_RBP_ID_8875684,Human_RBP_ID_9261171,Human_RBP_ID_9302565,Human_RBP_ID_9394312,Human_RBP_ID_18013023,Human_RBP_ID_19011124,Human_RBP_ID_26347472 Human_Splice_Rec_516446,Human_Splice_Rec_516456,Human_Splice_Rec_516464,Human_Splice_Rec_516470,Human_Splice_Rec_516510,Human_Splice_Rec_516514,Human_Splice_Rec_516520,Human_Splice_Rec_516522 RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_20912,RMVar_hsa_circ_71174 55671 RMVar_ID_55671 Human_SNP_ID_166423720 m1A Human chr3 + 184300401 184300401 184300401 GCCTCTCAAATTTCTGCGTCCACACTATGGCAAACTGAAGGAAATCTATGAGAACATGGCCCCTG GCCTCTCAAATTTCTGCGTCCACACTATGGCAGACTGAAGGAAATCTATGAGAACATGGCCCCTG A G PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184300351..184300425 26863196 MeRIP-seq:(Medium) rs1352216468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596588,Human_RBP_ID_1623286,Human_RBP_ID_1957443,Human_RBP_ID_8236118,Human_RBP_ID_9261172,Human_RBP_ID_9394313,Human_RBP_ID_14745111 Human_Splice_Rec_516447,Human_Splice_Rec_516457,Human_Splice_Rec_516465,Human_Splice_Rec_516471,Human_Splice_Rec_516515,Human_Splice_Rec_516523 Human_miRNA_ID_549442,Human_miRNA_ID_1136686,Human_miRNA_ID_1139201,Human_miRNA_ID_2534038,Human_miRNA_ID_2535770 RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_20912,RMVar_hsa_circ_71174 55672 RMVar_ID_55672 Human_SNP_ID_166423721 m1A Human chr3 + 184300401 184300401 184300401 GCCTCTCAAATTTCTGCGTCCACACTATGGCAAACTGAAGGAAATCTATGAGAACATGGCCCCTG GCCTCTCAAATTTCTGCGTCCACACTATGGCATACTGAAGGAAATCTATGAGAACATGGCCCCTG A T PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184300351..184300425 26863196 MeRIP-seq:(Medium) rs1352216468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596588,Human_RBP_ID_1623286,Human_RBP_ID_1957443,Human_RBP_ID_8236118,Human_RBP_ID_9261172,Human_RBP_ID_9394313,Human_RBP_ID_14745111 Human_Splice_Rec_516447,Human_Splice_Rec_516457,Human_Splice_Rec_516465,Human_Splice_Rec_516471,Human_Splice_Rec_516515,Human_Splice_Rec_516523 Human_miRNA_ID_549442,Human_miRNA_ID_1136686,Human_miRNA_ID_1139201,Human_miRNA_ID_2534038,Human_miRNA_ID_2535770 RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_20912,RMVar_hsa_circ_71174 55673 RMVar_ID_55673 Human_SNP_ID_166424122 m1A Human chr3 + 184301895 184301895 184301895 GTGGCTAAGGAGTGGCAGGAGCTGGATGACGCAGAGAAGGTCCAGCGGGAGCCTCTGCTCACTCT GTGGCTAAGGAGTGGCAGGAGCTGGATGACGCGGAGAAGGTCCAGCGGGAGCCTCTGCTCACTCT A G PSMD2 Ensembl:ENSG00000175166 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184301814..184301950 32194978 MeRIP-seq:(Medium) rs1279518112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247863,Human_RBP_ID_4733358,Human_RBP_ID_5149818,Human_RBP_ID_8875220,Human_RBP_ID_9302567,Human_RBP_ID_19013214,Human_RBP_ID_19116361,Human_RBP_ID_22457091,Human_RBP_ID_26346340,Human_RBP_ID_26771268 Human_Splice_Rec_516474,Human_Splice_Rec_516518,Human_Splice_Rec_516534,Human_Splice_Rec_516570 Human_miRNA_ID_3116418 RMVar_hsa_circ_83352,RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_71174,RMVar_hsa_circ_95935,RMVar_hsa_circ_106166,RMVar_hsa_circ_223345,RMVar_hsa_circ_223346,RMVar_hsa_circ_290355,RMVar_hsa_circ_223347,RMVar_hsa_circ_223349,RMVar_hsa_circ_119144 55674 RMVar_ID_55674 Human_SNP_ID_166424320 m1A Human chr3 + 184302482 184302482 184302482 TCCCTGAAGCTCTGAGATTGGCATTGATGCTCAATGACATGGAGTTGGTAGAAGACATCTTCACC TCCCTGAAGCTCTGAGATTGGCATTGATGCTCCATGACATGGAGTTGGTAGAAGACATCTTCACC A C PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184302432..184302549 26863196 MeRIP-seq:(Medium) rs767466862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596594,Human_RBP_ID_1957453,Human_RBP_ID_9395735,Human_RBP_ID_14745124,Human_RBP_ID_24535589 Human_Splice_Rec_516451,Human_Splice_Rec_516477,Human_Splice_Rec_516529,Human_Splice_Rec_516537,Human_Splice_Rec_516573,Human_Splice_Rec_516611,Human_Splice_Rec_516613 Human_miRNA_ID_2938147 RMVar_hsa_circ_83352,RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_71174,RMVar_hsa_circ_95935,RMVar_hsa_circ_106166,RMVar_hsa_circ_223345,RMVar_hsa_circ_223346,RMVar_hsa_circ_290355,RMVar_hsa_circ_54591,RMVar_hsa_circ_127780,RMVar_hsa_circ_223347,RMVar_hsa_circ_223349,RMVar_hsa_circ_119144,RMVar_hsa_circ_351976,RMVar_hsa_circ_74682,RMVar_hsa_circ_223350 55675 RMVar_ID_55675 Human_SNP_ID_166425264 m1A Human chr3 - 184305834 184305834 184305834 TGACTTCTCCATGATGGTCTGAAGGATAGTGGAAGTTACATCTCCATTGCAGGACCCTACTGCTA TGACTTCTCCATGATGGTCTGAAGGATAGTGGCAGTTACATCTCCATTGCAGGACCCTACTGCTA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184304363..184305840 32194978 MeRIP-seq:(Medium) rs942380887 Functional Loss SNV dbSNP153 33..33 33 - - - 55676 RMVar_ID_55676 Human_SNP_ID_166425559 m1A Human chr3 - 184306783 184306783 184306783 AATGCCATCTCTGCACCAATCTCCTCCCCCATAGCAATAAGGGCAATCCCCAGAACAGCCACTCC AATGCCATCTCTGCACCAATCTCCTCCCCCATGGCAATAAGGGCAATCCCCAGAACAGCCACTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:184306751..184306800 26863196 MeRIP-seq:(Medium) rs1449777891 Functional Loss SNV dbSNP153 33..33 33 - - - 55677 RMVar_ID_55677 Human_SNP_ID_166427753 m1A Human chr3 - 184314622 184314622 184314622 CGCGGCCGAGCCCCACGCAGCCGCACAGACGTAGTCCACAACCATTTCCGGCTCCCCGCACAGAT CGCGGCCGAGCCCCACGCAGCCGCACAGACGTCGTCCACAACCATTTCCGGCTCCCCGCACAGAT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr3:184314576..184314650;chr3:184314526..184314719 26863196 MeRIP-seq:(Medium) rs959262094 Functional Loss SNV dbSNP153 33..33 33 - - - 55678 RMVar_ID_55678 Human_SNP_ID_166427757 m1A Human chr3 - 184314628 184314628 184314628 AGTCCGCGCGGCCGAGCCCCACGCAGCCGCACAGACGTAGTCCACAACCATTTCCGGCTCCCCGC AGTCCGCGCGGCCGAGCCCCACGCAGCCGCACGGACGTAGTCCACAACCATTTCCGGCTCCCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184314551..184314716 26863196 MeRIP-seq:(Medium) rs1191351846 Functional Loss SNV dbSNP153 33..33 33 - - - 55679 RMVar_ID_55679 Human_SNP_ID_166427864 m1A Human chr3 - 184314915 184314915 184314915 GCATTTCGCGGCGACGAACCCGGCGCCCTACCAGCCCGCGGGGCCCGCATAGTCCGGCCCTGCGC GCATTTCGCGGCGACGAACCCGGCGCCCTACCCGCCCGCGGGGCCCGCATAGTCCGGCCCTGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184314911..184315003 26863196 MeRIP-seq:(Medium) rs1239893313 Functional Loss SNV dbSNP153 33..33 33 - - - 55680 RMVar_ID_55680 Human_SNP_ID_166427887 m1A Human chr3 + 184314990 184314990 184314990 TGACCCGAGGAGGCCCGGCAGCCCACGGGCGCAGGCACCACGGCTCCCGGCCCGCCGCCCCCTCC TGACCCGAGGAGGCCCGGCAGCCCACGGGCGCGGGCACCACGGCTCCCGGCCCGCCGCCCCCTCC A G EIF4G1 Ensembl:ENSG00000114867 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184314985..184315067 26863196 MeRIP-seq:(Medium) rs1357738193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596615,Human_RBP_ID_5207163,Human_RBP_ID_5392309,Human_RBP_ID_18464740,Human_RBP_ID_18499851 RMVar_hsa_circ_111936,RMVar_hsa_circ_223367,RMVar_hsa_circ_103560,RMVar_hsa_circ_223366 55681 RMVar_ID_55681 Human_SNP_ID_166428131 m1A Human chr3 + 184315526 184315526 184315526 CGGATGCCCAGAACCTGTAGGCCGCACCGTGGACTTGTTCTTAATCGAGGGGGTGAGTGAGGGGT CGGATGCCCAGAACCTGTAGGCCGCACCGTGGGCTTGTTCTTAATCGAGGGGGTGAGTGAGGGGT A G EIF4G1 Ensembl:ENSG00000114867 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184315476..184315550 26863196 MeRIP-seq:(Medium) rs1205830830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934591,Human_RBP_ID_1623304,Human_RBP_ID_1957477,Human_RBP_ID_3699290,Human_RBP_ID_3964452,Human_RBP_ID_4733469,Human_RBP_ID_7167706,Human_RBP_ID_8567070,Human_RBP_ID_8870113,Human_RBP_ID_8943526,Human_RBP_ID_14745169,Human_RBP_ID_18803686,Human_RBP_ID_22457594,Human_RBP_ID_24382396,Human_RBP_ID_26346343 Human_Splice_Rec_516730,Human_Splice_Rec_516731,Human_Splice_Rec_516976,Human_Splice_Rec_516977,Human_Splice_Rec_517042,Human_Splice_Rec_517043,Human_Splice_Rec_517074,Human_Splice_Rec_517075,Human_Splice_Rec_517108,Human_Splice_Rec_517109,Human_Splice_Rec_517236,Human_Splice_Rec_517237,Human_Splice_Rec_517240,Human_Splice_Rec_517241,Human_Splice_Rec_517252,Human_Splice_Rec_517253,Human_Splice_Rec_517265,Human_Splice_Rec_517323 RMVar_hsa_circ_19071,RMVar_hsa_circ_94159,RMVar_hsa_circ_111936,RMVar_hsa_circ_223367,RMVar_hsa_circ_103560,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223368,RMVar_hsa_circ_223369 55682 RMVar_ID_55682 Human_SNP_ID_166428205 m1A Human chr3 - 184315754 184315754 184315754 GCCACATCAGGGTCCCCCCAGCACCTGTTGGGAAAGAGTGGCGCTCAGGAAGAGGAAGGGACCCA GCCACATCAGGGTCCCCCCAGCACCTGTTGGGGAAGAGTGGCGCTCAGGAAGAGGAAGGGACCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184315751..184315875 26863196 MeRIP-seq:(Medium) rs1433600359 Functional Loss SNV dbSNP153 33..33 33 - - - 55683 RMVar_ID_55683 Human_SNP_ID_166430078 m1A Human chr3 - 184321451 184321451 184321451 GATTCTTCTACAGACATTTGTATAGTTGTCATAGTGTCCCCAGGAATAGAGAGGACTGCGAGATT GATTCTTCTACAGACATTTGTATAGTTGTCATCGTGTCCCCAGGAATAGAGAGGACTGCGAGATT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184321401..184321475 32194978 MeRIP-seq:(Medium) rs1257042290 Functional Loss SNV dbSNP153 33..33 33 - - - 55684 RMVar_ID_55684 Human_SNP_ID_166430088 m1A Human chr3 + 184321477 184321474 184321477 GGACACTATGACAACTATACAAATGTCTGTAGAAGAATCAACCCCCATCTCCCGTGAAACTGGGG GGACACTATGACAACTATACAAATGTCTGT___AGAATCAACCCCCATCTCCCGTGAAACTGGGG TAGA T EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:184321426..184321500 26863196 MeRIP-seq:(Medium) rs1189312824 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_67236,Human_RBP_ID_1623337,Human_RBP_ID_1957497,Human_RBP_ID_4763296,Human_RBP_ID_8567094,Human_RBP_ID_8870134,Human_RBP_ID_9261193,Human_RBP_ID_9333974,Human_RBP_ID_14745240,Human_RBP_ID_17289369,Human_RBP_ID_17518770,Human_RBP_ID_18803716,Human_RBP_ID_18954769,Human_RBP_ID_23020912,Human_RBP_ID_27049693,Human_RBP_ID_27316084 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 55685 RMVar_ID_55685 Human_SNP_ID_166430089 m1A Human chr3 + 184321481 184321481 184321481 ACTATGACAACTATACAAATGTCTGTAGAAGAATCAACCCCCATCTCCCGTGAAACTGGGGAGCC ACTATGACAACTATACAAATGTCTGTAGAAGAGTCAACCCCCATCTCCCGTGAAACTGGGGAGCC A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184321354..184321637 26863196 MeRIP-seq:(Medium) rs747516144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67236,Human_RBP_ID_1623337,Human_RBP_ID_1957497,Human_RBP_ID_4733518,Human_RBP_ID_8567094,Human_RBP_ID_8870134,Human_RBP_ID_9261193,Human_RBP_ID_9333974,Human_RBP_ID_14745240,Human_RBP_ID_17289369,Human_RBP_ID_17402752,Human_RBP_ID_17518770,Human_RBP_ID_18001231,Human_RBP_ID_18803716,Human_RBP_ID_18954769,Human_RBP_ID_23020912,Human_RBP_ID_27049693,Human_RBP_ID_27316084 Human_miRNA_ID_3011330,Human_miRNA_ID_3011331 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 55686 RMVar_ID_55686 Human_SNP_ID_166430113 m1A Human chr3 - 184321538 184321538 184321538 ACTTCTACTTCCAGTATGGGTTCGGCGAGAGGAGTGGGTTCTGGAGAGAGGCGATATGGCTCCCC ACTTCTACTTCCAGTATGGGTTCGGCGAGAGGCGTGGGTTCTGGAGAGAGGCGATATGGCTCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184321489..184321635 26863196 MeRIP-seq:(Medium) rs780291897 Functional Loss SNV dbSNP153 33..33 33 - - - 55687 RMVar_ID_55687 Human_SNP_ID_166430304 m1A Human chr3 + 184321975 184321973 184321976 GGAGGAGGAAATGGAAGAAGAAGAAGAAGAGGAAGAAGGAGAAGCAGGAGAAGCAGGAGAAGCTG GGAGGAGGAAATGGAAGAAGAAGAAGAAGAG___GAAGGAGAAGCAGGAGAAGCAGGAGAAGCTG GGAA G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184321926..184322000 26863196 MeRIP-seq:(Medium) rs1307902699 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1957504,Human_RBP_ID_4733550,Human_RBP_ID_7167757,Human_RBP_ID_8567104,Human_RBP_ID_22533949,Human_RBP_ID_23020920,Human_RBP_ID_23989285,Human_RBP_ID_24547350,Human_RBP_ID_26346352,Human_RBP_ID_27822785 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 55688 RMVar_ID_55688 Human_SNP_ID_166430655 m1A Human chr3 + 184322843 184322843 184322843 TTCCTTGCAGATCAGTGGAAGCCTCTAAACCTAGAGGAGAAAAAACGTTACGACCGTGAGTTCCT TTCCTTGCAGATCAGTGGAAGCCTCTAAACCTCGAGGAGAAAAAACGTTACGACCGTGAGTTCCT A C EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184322826..184322850 32194978 MeRIP-seq:(Medium) rs1026246161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1623364,Human_RBP_ID_1957513,Human_RBP_ID_8870167,Human_RBP_ID_9394345,Human_RBP_ID_22092883,Human_RBP_ID_23989287 Human_Splice_Rec_516688,Human_Splice_Rec_516752,Human_Splice_Rec_516810,Human_Splice_Rec_516872,Human_Splice_Rec_516934,Human_Splice_Rec_516966,Human_Splice_Rec_517000,Human_Splice_Rec_517060,Human_Splice_Rec_517094,Human_Splice_Rec_517130,Human_Splice_Rec_517186,Human_Splice_Rec_517282,Human_Splice_Rec_517344,Human_Splice_Rec_517406,Human_Splice_Rec_517474,Human_Splice_Rec_517528,Human_Splice_Rec_517556,Human_Splice_Rec_517612,Human_Splice_Rec_517678 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374 55689 RMVar_ID_55689 Human_SNP_ID_166430882 m1A Human chr3 + 184323535 184323535 184323535 CAAAGCAGAGAAAGCCTGGAAACCCAGCAGCAAGCGGACGGCGGCTGATAAGGATCGAGGGGAAG CAAAGCAGAGAAAGCCTGGAAACCCAGCAGCAGGCGGACGGCGGCTGATAAGGATCGAGGGGAAG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184323394..184323590 26863196 MeRIP-seq:(Medium) rs905875693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247258,Human_RBP_ID_835804,Human_RBP_ID_937583,Human_RBP_ID_1623374,Human_RBP_ID_1957520,Human_RBP_ID_4733595,Human_RBP_ID_5607114,Human_RBP_ID_8567128,Human_RBP_ID_8875286,Human_RBP_ID_9261199,Human_RBP_ID_9302637,Human_RBP_ID_9334377,Human_RBP_ID_9394351,Human_RBP_ID_22745384,Human_RBP_ID_23027358,Human_RBP_ID_24547352,Human_RBP_ID_26346356,Human_RBP_ID_27049717,Human_RBP_ID_27822788 Human_Splice_Rec_516693,Human_Splice_Rec_516757,Human_Splice_Rec_516815,Human_Splice_Rec_516877,Human_Splice_Rec_516939,Human_Splice_Rec_516971,Human_Splice_Rec_517005,Human_Splice_Rec_517065,Human_Splice_Rec_517099,Human_Splice_Rec_517135,Human_Splice_Rec_517191,Human_Splice_Rec_517287,Human_Splice_Rec_517349,Human_Splice_Rec_517411,Human_Splice_Rec_517479,Human_Splice_Rec_517533,Human_Splice_Rec_517561,Human_Splice_Rec_517617,Human_Splice_Rec_517683 Human_miRNA_ID_2524685,Human_miRNA_ID_2524686,Human_miRNA_ID_3010302,Human_miRNA_ID_3010303 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_54287,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374 55690 RMVar_ID_55690 Human_SNP_ID_166431260 m1A Human chr3 - 184324849 184324849 184324849 CTGCCTGCCATTCACAGGACAGGGATTGTGTCAAAAAGATAACCAGCCACTCGGCTAAAACCCTT CTGCCTGCCATTCACAGGACAGGGATTGTGTCTAAAAGATAACCAGCCACTCGGCTAAAACCCTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184324846..184325149 26863196 MeRIP-seq:(Medium) rs757102049 Functional Loss SNV dbSNP153 33..33 33 - - - 55691 RMVar_ID_55691 Human_SNP_ID_166431261 m1A Human chr3 - 184324849 184324849 184324849 CTGCCTGCCATTCACAGGACAGGGATTGTGTCAAAAAGATAACCAGCCACTCGGCTAAAACCCTT CTGCCTGCCATTCACAGGACAGGGATTGTGTCGAAAAGATAACCAGCCACTCGGCTAAAACCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184324846..184325149 26863196 MeRIP-seq:(Medium) rs757102049 Functional Loss SNV dbSNP153 33..33 33 - - - 55692 RMVar_ID_55692 Human_SNP_ID_166431287 m1A Human chr3 + 184324926 184324926 184324926 GCCTGAAGGAAGAGCTGGAAGAGGCTCGGGACATAGCCCGGCGGCGCTCTTTAGGGAATATCAAG GCCTGAAGGAAGAGCTGGAAGAGGCTCGGGACGTAGCCCGGCGGCGCTCTTTAGGGAATATCAAG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184324872..184325032 26863196 MeRIP-seq:(Medium) rs373331022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247259,Human_RBP_ID_4733619,Human_RBP_ID_5447304,Human_RBP_ID_7167787,Human_RBP_ID_8870201,Human_RBP_ID_9261206,Human_RBP_ID_9303126,Human_RBP_ID_9394358,Human_RBP_ID_14745282,Human_RBP_ID_17703454,Human_RBP_ID_18001240,Human_RBP_ID_23026778,Human_RBP_ID_26347502 Human_Splice_Rec_516698,Human_Splice_Rec_516762,Human_Splice_Rec_516820,Human_Splice_Rec_516882,Human_Splice_Rec_517010,Human_Splice_Rec_517070,Human_Splice_Rec_517104,Human_Splice_Rec_517140,Human_Splice_Rec_517196,Human_Splice_Rec_517292,Human_Splice_Rec_517354,Human_Splice_Rec_517416,Human_Splice_Rec_517484,Human_Splice_Rec_517538,Human_Splice_Rec_517566,Human_Splice_Rec_517622,Human_Splice_Rec_517688 Human_miRNA_ID_2442815,Human_miRNA_ID_2442816 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_54287,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374,RMVar_hsa_circ_309763,RMVar_hsa_circ_351209 55693 RMVar_ID_55693 Human_SNP_ID_166431503 m1A Human chr3 + 184325583 184325583 184325583 GGAAGAACATCGAGAGCACATCAAAGTGCAGCAGCTCATGGCCAAGGGCAGTGACAAGCGTCGGG GGAAGAACATCGAGAGCACATCAAAGTGCAGCGGCTCATGGCCAAGGGCAGTGACAAGCGTCGGG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184325533..184325661 26863196 MeRIP-seq:(Medium) rs1456865027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1623399,Human_RBP_ID_1957533,Human_RBP_ID_3699323,Human_RBP_ID_7167802,Human_RBP_ID_8567144,Human_RBP_ID_8870219,Human_RBP_ID_17518790,Human_RBP_ID_18194751,Human_RBP_ID_26348593,Human_RBP_ID_26825141,Human_RBP_ID_27049739 Human_Splice_Rec_516703,Human_Splice_Rec_516767,Human_Splice_Rec_516825,Human_Splice_Rec_516887,Human_Splice_Rec_517015,Human_Splice_Rec_517145,Human_Splice_Rec_517201,Human_Splice_Rec_517297,Human_Splice_Rec_517359,Human_Splice_Rec_517421,Human_Splice_Rec_517489,Human_Splice_Rec_517571,Human_Splice_Rec_517627,Human_Splice_Rec_517693,Human_Splice_Rec_517723,Human_Splice_Rec_517731 Human_miRNA_ID_633924,Human_miRNA_ID_2217119,Human_miRNA_ID_2217120,Human_miRNA_ID_2392556,Human_miRNA_ID_2392557,Human_miRNA_ID_2893598,Human_miRNA_ID_2893599 RMVar_hsa_circ_28932,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_364941 55694 RMVar_ID_55694 Human_SNP_ID_166431992 m1A Human chr3 + 184326982 184326982 184326982 CAGAAAGCACAGATAATAGACGTGTGGTGCAGAGGTGAGGTTTCCTGGACATCTTTGTTATTCAC CAGAAAGCACAGATAATAGACGTGTGGTGCAGCGGTGAGGTTTCCTGGACATCTTTGTTATTCAC A C EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:184326859..184327020;chr3:184326901..184327000 26863196 MeRIP-seq:(Medium) rs371300800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1957545,Human_RBP_ID_8875309,Human_RBP_ID_9302648,Human_RBP_ID_18013579,Human_RBP_ID_19118999,Human_RBP_ID_26347511 Human_Splice_Rec_516709,Human_Splice_Rec_516773,Human_Splice_Rec_516831,Human_Splice_Rec_516893,Human_Splice_Rec_517021,Human_Splice_Rec_517151,Human_Splice_Rec_517207,Human_Splice_Rec_517303,Human_Splice_Rec_517365,Human_Splice_Rec_517427,Human_Splice_Rec_517495,Human_Splice_Rec_517577,Human_Splice_Rec_517633,Human_Splice_Rec_517699,Human_Splice_Rec_517729 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_100008,RMVar_hsa_circ_109512,RMVar_hsa_circ_223377 55695 RMVar_ID_55695 Human_SNP_ID_166432113 m1A Human chr3 - 184327297 184327288 184327297 GCAGGTGTCCGCGCACGATCAAGCCGGTCCCCACGGTCCCCTCCCCGTTCACTCCGCTCTAGGCG GCAGGTGTCCGCGCACGATCAAGCCGGTCCCC_________TCCCCGTTCACTCCGCTCTAGGCG AGGGGACCGT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:184327251..184327300 26863196 MeRIP-seq:(Medium) rs1265725999 Functional Loss DEL dbSNP153 33..41 33 - - - 55696 RMVar_ID_55696 Human_SNP_ID_166432140 m1A Human chr3 + 184327331 184327331 184327331 GGGACCGGCTTGATCGTGCGCGGACACCTGCTACCAAGCGGAGCTTCAGCAAGGAAGTGGAGGAG GGGACCGGCTTGATCGTGCGCGGACACCTGCTGCCAAGCGGAGCTTCAGCAAGGAAGTGGAGGAG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184327201..184327453 26863196 MeRIP-seq:(Medium) rs753115052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67276,Human_RBP_ID_1623421,Human_RBP_ID_1957547,Human_RBP_ID_3699331,Human_RBP_ID_3964457,Human_RBP_ID_4763370,Human_RBP_ID_7167820,Human_RBP_ID_8870240,Human_RBP_ID_9261212,Human_RBP_ID_9301475,Human_RBP_ID_9394378,Human_RBP_ID_18803792,Human_RBP_ID_22456351,Human_RBP_ID_26346365 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 55697 RMVar_ID_55697 Human_SNP_ID_166432151 m1A Human chr3 + 184327359 184327359 184327359 TGCTACCAAGCGGAGCTTCAGCAAGGAAGTGGAGGAGCGGAGTAGAGAACGGCCCTCCCAGCCTG TGCTACCAAGCGGAGCTTCAGCAAGGAAGTGGGGGAGCGGAGTAGAGAACGGCCCTCCCAGCCTG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1453842038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67276,Human_RBP_ID_1069240,Human_RBP_ID_1623422,Human_RBP_ID_1957547,Human_RBP_ID_3699331,Human_RBP_ID_3965780,Human_RBP_ID_5205987,Human_RBP_ID_7167820,Human_RBP_ID_8870240,Human_RBP_ID_9303142,Human_RBP_ID_9395765,Human_RBP_ID_24547354,Human_RBP_ID_26346366,Human_RBP_ID_27822792 Human_Splice_Rec_516711,Human_Splice_Rec_516775,Human_Splice_Rec_516833,Human_Splice_Rec_516895,Human_Splice_Rec_517023,Human_Splice_Rec_517153,Human_Splice_Rec_517209,Human_Splice_Rec_517305,Human_Splice_Rec_517367,Human_Splice_Rec_517429,Human_Splice_Rec_517497,Human_Splice_Rec_517579,Human_Splice_Rec_517635,Human_Splice_Rec_517701,Human_Splice_Rec_517737 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 55698 RMVar_ID_55698 Human_SNP_ID_166432152 m1A Human chr3 + 184327359 184327359 184327359 TGCTACCAAGCGGAGCTTCAGCAAGGAAGTGGAGGAGCGGAGTAGAGAACGGCCCTCCCAGCCTG TGCTACCAAGCGGAGCTTCAGCAAGGAAGTGGTGGAGCGGAGTAGAGAACGGCCCTCCCAGCCTG A T EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1453842038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67276,Human_RBP_ID_1069240,Human_RBP_ID_1623422,Human_RBP_ID_1957547,Human_RBP_ID_3699331,Human_RBP_ID_3965780,Human_RBP_ID_5205987,Human_RBP_ID_7167820,Human_RBP_ID_8870240,Human_RBP_ID_9303142,Human_RBP_ID_9395765,Human_RBP_ID_24547354,Human_RBP_ID_26346366,Human_RBP_ID_27822792 Human_Splice_Rec_516711,Human_Splice_Rec_516775,Human_Splice_Rec_516833,Human_Splice_Rec_516895,Human_Splice_Rec_517023,Human_Splice_Rec_517153,Human_Splice_Rec_517209,Human_Splice_Rec_517305,Human_Splice_Rec_517367,Human_Splice_Rec_517429,Human_Splice_Rec_517497,Human_Splice_Rec_517579,Human_Splice_Rec_517635,Human_Splice_Rec_517701,Human_Splice_Rec_517737 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 55699 RMVar_ID_55699 Human_SNP_ID_166432163 m1A Human chr3 + 184327375 184327375 184327375 TTCAGCAAGGAAGTGGAGGAGCGGAGTAGAGAACGGCCCTCCCAGCCTGAGGGGCTGCGCAAGGC TTCAGCAAGGAAGTGGAGGAGCGGAGTAGAGAGCGGCCCTCCCAGCCTGAGGGGCTGCGCAAGGC A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:184327351..184327375 26863196 MeRIP-seq:(Medium) rs1222571303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67276,Human_RBP_ID_596651,Human_RBP_ID_937594,Human_RBP_ID_1069240,Human_RBP_ID_8236120,Human_RBP_ID_9302650,Human_RBP_ID_24384074,Human_RBP_ID_24547354,Human_RBP_ID_26346366,Human_RBP_ID_27822792 Human_Splice_Rec_516711,Human_Splice_Rec_516775,Human_Splice_Rec_516833,Human_Splice_Rec_516895,Human_Splice_Rec_517023,Human_Splice_Rec_517153,Human_Splice_Rec_517209,Human_Splice_Rec_517305,Human_Splice_Rec_517367,Human_Splice_Rec_517429,Human_Splice_Rec_517497,Human_Splice_Rec_517579,Human_Splice_Rec_517635,Human_Splice_Rec_517701,Human_Splice_Rec_517737 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 55700 RMVar_ID_55700 Human_SNP_ID_166432273 m1A Human chr3 - 184327622 184327622 184327622 TCTCTAACTCCTCCTCAGAGAGAGCCGCCTTCAGGGGGCTCACTGGGGGTAGGGCAGCTTCTCGC TCTCTAACTCCTCCTCAGAGAGAGCCGCCTTCGGGGGGCTCACTGGGGGTAGGGCAGCTTCTCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184325471..184327767 32194978 MeRIP-seq:(Medium) rs2230570 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 55701 RMVar_ID_55701 Human_SNP_ID_166432288 m1A Human chr3 + 184327663 184327663 184327663 CTCTCTCTGAGGAGGAGTTAGAGAAGAAATCCAAGGCTATCATTGAGGAATATCTCCATCTCAAT CTCTCTCTGAGGAGGAGTTAGAGAAGAAATCCGAGGCTATCATTGAGGAATATCTCCATCTCAAT A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184327601..184327675 26863196 MeRIP-seq:(Medium) rs751252151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67278,Human_RBP_ID_934601,Human_RBP_ID_1623425,Human_RBP_ID_1957549,Human_RBP_ID_7167829,Human_RBP_ID_8567164,Human_RBP_ID_8870250,Human_RBP_ID_9394381,Human_RBP_ID_17518794,Human_RBP_ID_18535881,Human_RBP_ID_18803793,Human_RBP_ID_22822876,Human_RBP_ID_26346367 Human_Splice_Rec_516712,Human_Splice_Rec_516713,Human_Splice_Rec_516776,Human_Splice_Rec_516777,Human_Splice_Rec_516834,Human_Splice_Rec_516835,Human_Splice_Rec_516896,Human_Splice_Rec_516897,Human_Splice_Rec_517024,Human_Splice_Rec_517025,Human_Splice_Rec_517154,Human_Splice_Rec_517155,Human_Splice_Rec_517210,Human_Splice_Rec_517211,Human_Splice_Rec_517306,Human_Splice_Rec_517307,Human_Splice_Rec_517368,Human_Splice_Rec_517369,Human_Splice_Rec_517430,Human_Splice_Rec_517431,Human_Splice_Rec_517498,Human_Splice_Rec_517499,Human_Splice_Rec_517580,Human_Splice_Rec_517581,Human_Splice_Rec_517636,Human_Splice_Rec_517637,Human_Splice_Rec_517702,Human_Splice_Rec_517703,Human_Splice_Rec_517738 Human_miRNA_ID_136232,Human_miRNA_ID_2377581,Human_miRNA_ID_2377582,Human_miRNA_ID_2997807,Human_miRNA_ID_2997808,Human_miRNA_ID_3092656,Human_miRNA_ID_3092657 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_309763,RMVar_hsa_circ_72349,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512,RMVar_hsa_circ_223378,RMVar_hsa_circ_359388 55702 RMVar_ID_55702 Human_SNP_ID_166432662 m1A Human chr3 - 184328758 184328758 184328758 TTACCTCCCCTGAATTCCACCCAGGGGGACTTACCTGAACAGCTCCCCCATGGGCACCCCACCTT TTACCTCCCCTGAATTCCACCCAGGGGGACTTCCCTGAACAGCTCCCCCATGGGCACCCCACCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184328726..184328775 32194978 MeRIP-seq:(Medium) rs879112085 Functional Loss SNV dbSNP153 33..33 33 - - - 55703 RMVar_ID_55703 Human_SNP_ID_166433492 m1A Human chr3 + 184331605 184331605 184331605 CAGCAGTAACCAGCGGGTGTTCGACTGGATAGAGGTAGGTTTCTCCTGGATATCGATAAAGGAAA CAGCAGTAACCAGCGGGTGTTCGACTGGATAGTGGTAGGTTTCTCCTGGATATCGATAAAGGAAA A T EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184331576..184331625 26863196 MeRIP-seq:(Medium) rs1329906906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933466,Human_RBP_ID_3964462,Human_RBP_ID_8567181,Human_RBP_ID_9303160,Human_RBP_ID_19119008,Human_RBP_ID_22455667,Human_RBP_ID_27823800 Human_Splice_Rec_516723,Human_Splice_Rec_516787,Human_Splice_Rec_516845,Human_Splice_Rec_516907,Human_Splice_Rec_517035,Human_Splice_Rec_517165,Human_Splice_Rec_517221,Human_Splice_Rec_517317,Human_Splice_Rec_517379,Human_Splice_Rec_517441,Human_Splice_Rec_517509,Human_Splice_Rec_517591,Human_Splice_Rec_517647,Human_Splice_Rec_517713,Human_Splice_Rec_517747,Human_Splice_Rec_517755,Human_Splice_Rec_517767,Human_Splice_Rec_517777,Human_Splice_Rec_517781 RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 55704 RMVar_ID_55704 Human_SNP_ID_166433945 m1A Human chr3 - 184332937 184332937 184332937 AAATTCCTTTATTCCTTGCTTAAAATCCCACAAAGGCGTTTTCTTGCCCCCAGGCTAAAGCCCCA AAATTCCTTTATTCCTTGCTTAAAATCCCACAGAGGCGTTTTCTTGCCCCCAGGCTAAAGCCCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184332935..184333735 26863196 MeRIP-seq:(Medium) rs989838644 Functional Loss SNV dbSNP153 33..33 33 - - - 55705 RMVar_ID_55705 Human_SNP_ID_166434387 m1A Human chr3 + 184334901 184334901 184334901 GTGGCTCCGTGAAGCAGAGGAGGAGTCTGACCACAACTGAGGGCTGGTGGGGCCGGGGACCTGGA GTGGCTCCGTGAAGCAGAGGAGGAGTCTGACCGCAACTGAGGGCTGGTGGGGCCGGGGACCTGGA A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184334723..184335144 26863196 MeRIP-seq:(Medium) rs1470725487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596670,Human_RBP_ID_1032281,Human_RBP_ID_1069244,Human_RBP_ID_1623468,Human_RBP_ID_1957587,Human_RBP_ID_3699350,Human_RBP_ID_4733752,Human_RBP_ID_5120443,Human_RBP_ID_7167904,Human_RBP_ID_8567193,Human_RBP_ID_8870290,Human_RBP_ID_9261224,Human_RBP_ID_9301488,Human_RBP_ID_9394388,Human_RBP_ID_14745495,Human_RBP_ID_17289385,Human_RBP_ID_17661241,Human_RBP_ID_18001260,Human_RBP_ID_18194970,Human_RBP_ID_18424437,Human_RBP_ID_18803831,Human_RBP_ID_22455670,Human_RBP_ID_26506084,Human_RBP_ID_27316140 RMVar_hsa_circ_105927,RMVar_hsa_circ_223373 55706 RMVar_ID_55706 Human_SNP_ID_166442410 m1A Human chr3 - 184361497 184361497 184361497 CCAGGACAGAGCCGGAACCGCCGAGGGAGGCGAGAGGGCAGTGCGCGGAGATGGCGGCCGCGGCG CCAGGACAGAGCCGGAACCGCCGAGGGAGGCGTGAGGGCAGTGCGCGGAGATGGCGGCCGCGGCG T A CLCN2 Ensembl:ENSG00000114859 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184361460..184361541 26863196 MeRIP-seq:(Medium) rs1416577922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756866,Human_RBP_ID_8943528 Human_Splice_Rec_517867,Human_Splice_Rec_517913,Human_Splice_Rec_518003,Human_Splice_Rec_518067,Human_Splice_Rec_518103,Human_Splice_Rec_518143,Human_Splice_Rec_518187,Human_Splice_Rec_518265,Human_Splice_Rec_518291,Human_Splice_Rec_518377 55707 RMVar_ID_55707 Human_SNP_ID_166443406 m1A Human chr3 + 184365155 184365155 184365155 TTATTTTCAGGTGACAAGTTTCGGTTGGTCATAGCTAGTACCTTGTATGAAGATGGTACCCTGGA TTATTTTCAGGTGACAAGTTTCGGTTGGTCATCGCTAGTACCTTGTATGAAGATGGTACCCTGGA A C POLR2H Ensembl:ENSG00000163882 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184365126..184365295 32194978 MeRIP-seq:(Medium) rs759838883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70196,Human_RBP_ID_248446,Human_RBP_ID_596700,Human_RBP_ID_936137,Human_RBP_ID_1623523,Human_RBP_ID_1957599,Human_RBP_ID_5120447,Human_RBP_ID_5390387,Human_RBP_ID_14745859,Human_RBP_ID_18013036,Human_RBP_ID_19011148,Human_RBP_ID_22457603,Human_RBP_ID_22551907,Human_RBP_ID_22745442,Human_RBP_ID_23989402,Human_RBP_ID_26348603 Human_Splice_Rec_518414,Human_Splice_Rec_518415,Human_Splice_Rec_518424,Human_Splice_Rec_518425,Human_Splice_Rec_518436,Human_Splice_Rec_518437,Human_Splice_Rec_518444,Human_Splice_Rec_518445,Human_Splice_Rec_518450,Human_Splice_Rec_518451,Human_Splice_Rec_518456,Human_Splice_Rec_518457,Human_Splice_Rec_518464,Human_Splice_Rec_518465,Human_Splice_Rec_518470,Human_Splice_Rec_518471,Human_Splice_Rec_518475,Human_Splice_Rec_518480 Human_miRNA_ID_755603,Human_miRNA_ID_1178130 RMVar_hsa_circ_276577,RMVar_hsa_circ_360341,RMVar_hsa_circ_223385 55708 RMVar_ID_55708 Human_SNP_ID_166447620 m1A Human chr3 + 184380405 184380404 184380405 CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCAGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCC_GAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA CA C CHRD Ensembl:ENSG00000090539 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1215932635 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5133530,Human_RBP_ID_9395775,Human_RBP_ID_18471739 Human_Splice_Rec_518553,Human_Splice_Rec_518569,Human_Splice_Rec_518613,Human_Splice_Rec_518659,Human_Splice_Rec_518703,Human_Splice_Rec_518733,Human_Splice_Rec_518777,Human_Splice_Rec_518819,Human_Splice_Rec_518857,Human_Splice_Rec_518859 55709 RMVar_ID_55709 Human_SNP_ID_166447621 m1A Human chr3 + 184380405 184380405 184380405 CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCAGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCCGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA A C CHRD Ensembl:ENSG00000090539 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1920128 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5133530,Human_RBP_ID_9395775,Human_RBP_ID_18471739 Human_Splice_Rec_518553,Human_Splice_Rec_518569,Human_Splice_Rec_518613,Human_Splice_Rec_518659,Human_Splice_Rec_518703,Human_Splice_Rec_518733,Human_Splice_Rec_518777,Human_Splice_Rec_518819,Human_Splice_Rec_518857,Human_Splice_Rec_518859 55710 RMVar_ID_55710 Human_SNP_ID_166447622 m1A Human chr3 + 184380405 184380405 184380405 CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCAGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCTGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA A T CHRD Ensembl:ENSG00000090539 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1920128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5133530,Human_RBP_ID_9395775,Human_RBP_ID_18471739 Human_Splice_Rec_518553,Human_Splice_Rec_518569,Human_Splice_Rec_518613,Human_Splice_Rec_518659,Human_Splice_Rec_518703,Human_Splice_Rec_518733,Human_Splice_Rec_518777,Human_Splice_Rec_518819,Human_Splice_Rec_518857,Human_Splice_Rec_518859 55711 RMVar_ID_55711 Human_SNP_ID_166496478 m1A Human chr3 + 184561836 184561836 184561836 GCGGCGCAGCAAGATCCCAGCTCGGACCCCGGACGGCGCGCGCCCCCGAAGCCCCGGATCCCAGT GCGGCGCAGCAAGATCCCAGCTCGGACCCCGGGCGGCGCGCGCCCCCGAAGCCCCGGATCCCAGT A G EPHB3 Ensembl:ENSG00000182580 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184561786..184561954 26863196 MeRIP-seq:(Medium) rs111982307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4733891 55712 RMVar_ID_55712 Human_SNP_ID_166496504 m1A Human chr3 + 184561901 184561901 184561901 CGGGCCCGCAGCTGACCGCCAGATTACTGTGCATCCCGAATCACGACCACCTGCACCCTCCTGCC CGGGCCCGCAGCTGACCGCCAGATTACTGTGCCTCCCGAATCACGACCACCTGCACCCTCCTGCC A C EPHB3 Ensembl:ENSG00000182580 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:184561812..184561983 26863410 MeRIP-seq:(Medium) rs550680399 Functional Loss SNV dbSNP153 33..33 33 - - - 55713 RMVar_ID_55713 Human_SNP_ID_166535544 m1A Human chr3 - 184711125 184711125 184711125 GATATCTCAGTTACAGGCGGGTGCCTCACACCAATCCACCAGAATATGAATTCTCTTGGGGTCCC GATATCTCAGTTACAGGCGGGTGCCTCACACCGATCCACCAGAATATGAATTCTCTTGGGGTCCC T C MAGEF1 Ensembl:ENSG00000177383 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184711076..184711200 32194978 MeRIP-seq:(Medium) rs778155185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22092894,Human_RBP_ID_23989494 55714 RMVar_ID_55714 Human_SNP_ID_166535833 m1A Human chr3 - 184711743 184711743 184711743 AGGGGGAGAAGGATGGCGGCCATGATGGTGAGACCCGGGCCCCGACCGCCTCGCAGGAGCGCCCC AGGGGGAGAAGGATGGCGGCCATGATGGTGAGTCCCGGGCCCCGACCGCCTCGCAGGAGCGCCCC T A MAGEF1 Ensembl:ENSG00000177383 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:184711465..184712028 26863196 MeRIP-seq:(Medium) rs1166228793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756869,Human_RBP_ID_5149833,Human_RBP_ID_9395793,Human_RBP_ID_27565981 55715 RMVar_ID_55715 Human_SNP_ID_166535895 m1A Human chr3 + 184711872 184711872 184711872 GCAGAGCGCGTACACGGGCCGAGGGGTGTGGGAGCCGCCGCGCAAGCCCCGGGGGAGGGGTTGGA GCAGAGCGCGTACACGGGCCGAGGGGTGTGGGGGCCGCCGCGCAAGCCCCGGGGGAGGGGTTGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:184711826..184711987;chr3:184711676..184711975 26863196 MeRIP-seq:(Medium) rs747719291 Functional Loss SNV dbSNP153 33..33 33 - - - 55716 RMVar_ID_55716 Human_SNP_ID_166535919 m1A Human chr3 + 184711937 184711937 184711937 CAGCGGCAGTGACGGCGGGAGTACAAGGAGCAATGGCAGCGGGAGCTTTGTGGCTGCTGGGCCGC CAGCGGCAGTGACGGCGGGAGTACAAGGAGCAGTGGCAGCGGGAGCTTTGTGGCTGCTGGGCCGC A G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:184711852..184711952 26863410 MeRIP-seq:(Medium) rs1482523899 Functional Loss SNV dbSNP153 33..33 33 - - - 55717 RMVar_ID_55717 Human_SNP_ID_166562851 m1A Human chr3 + 184812224 184812224 184812224 CGGCGGTCCACGGCCGGAATGGCAGCAAGCTCAGGTAACGAGTTTCCAGAGAGCGGGCCCGTGGA CGGCGGTCCACGGCCGGAATGGCAGCAAGCTCTGGTAACGAGTTTCCAGAGAGCGGGCCCGTGGA A T VPS8 Ensembl:ENSG00000156931 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184812203..184812298 26863196 MeRIP-seq:(Medium) rs755310288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757611,Human_RBP_ID_18424369 Human_Splice_Rec_519033,Human_Splice_Rec_519123,Human_Splice_Rec_519215,Human_Splice_Rec_519303,Human_Splice_Rec_519319,Human_Splice_Rec_519321 55718 RMVar_ID_55718 Human_SNP_ID_166666674 m1A Human chr3 - 185248516 185248515 185248516 GATTTACTTCATGTATTTTGTTTTCTTTTAGTACGACTTTACTCCGTGACATAAAAGAAGGACTA GATTTACTTCATGTATTTTGTTTTCTTTTAGT_CGACTTTACTCCGTGACATAAAAGAAGGACTA GT G EHHADH Ensembl:ENSG00000113790 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:185248482..185248567 26863410 MeRIP-seq:(Medium) rs1560023410 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9395798 Human_Splice_Rec_519642,Human_Splice_Rec_519654,Human_Splice_Rec_519668,Human_Splice_Rec_519678,Human_Splice_Rec_519682 RMVar_hsa_circ_367413,RMVar_hsa_circ_295664,RMVar_hsa_circ_223449,RMVar_hsa_circ_351233,RMVar_hsa_circ_350000 55719 RMVar_ID_55719 Human_SNP_ID_166674441 m1A Human chr3 - 185283044 185283044 185283044 AACTCCAGCTGCCACCCTCGCCCCCCGTTCAGATCCGCCCGCAGGTTACCTGTCGGGGATCCTAG AACTCCAGCTGCCACCCTCGCCCCCCGTTCAGTTCCGCCCGCAGGTTACCTGTCGGGGATCCTAG T A lnc-EHHADH-2 RNACentral:URS00008BB07B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:185283039..185283110 26863196 MeRIP-seq:(Medium) rs995086490 Functional Loss SNV dbSNP153 33..33 33 - - - 55720 RMVar_ID_55720 Human_SNP_ID_166676475 m1A Human chr3 + 185292304 185292303 185292305 TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTAAAAAAAAAAAAAAAGTTGAATTAACAATAAGG TCCAGCCTGGGTGACAGAGCGAGACTCCGTCT__AAAAAAAAAAAAAGTTGAATTAACAATAAGG TAA T MAP3K13 Ensembl:ENSG00000073803 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs754183268 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_79846,RMVar_hsa_circ_78256,RMVar_hsa_circ_223452,RMVar_hsa_circ_223453 55721 RMVar_ID_55721 Human_SNP_ID_166676479 m1A Human chr3 + 185292304 185292304 185292304 TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTAAAAAAAAAAAAAAAGTTGAATTAACAATAAGG TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTGAAAAAAAAAAAAAAGTTGAATTAACAATAAGG A G MAP3K13 Ensembl:ENSG00000073803 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1353562344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79846,RMVar_hsa_circ_78256,RMVar_hsa_circ_223452,RMVar_hsa_circ_223453 55722 RMVar_ID_55722 Human_SNP_ID_166676480 m1A Human chr3 + 185292304 185292304 185292304 TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTAAAAAAAAAAAAAAAGTTGAATTAACAATAAGG TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTTAAAAAAAAAAAAAAGTTGAATTAACAATAAGG A T MAP3K13 Ensembl:ENSG00000073803 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1353562344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79846,RMVar_hsa_circ_78256,RMVar_hsa_circ_223452,RMVar_hsa_circ_223453 55723 RMVar_ID_55723 Human_SNP_ID_166704645 m1A Human chr3 - 185417702 185417702 185417702 CTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCAGCACTACCAGCCAAATCAGATGAAAAGGCGGC CTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACCAGCCAAATCAGATGAAAAGGCGGC T C RPL4P4 Ensembl:ENSG00000229638 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879195525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1885991 55724 RMVar_ID_55724 Human_SNP_ID_166704727 m1A Human chr3 - 185418072 185418072 185418072 TGGAATTACTCTGCTTAATGTAAGCAAGCTGAACATTTTGAAGCTTGCTCCTGGTGGGCATGTGG TGGAATTACTCTGCTTAATGTAAGCAAGCTGAGCATTTTGAAGCTTGCTCCTGGTGGGCATGTGG T C RPL4P4 Ensembl:ENSG00000229638 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1356221615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1623618,Human_RBP_ID_1957793,Human_RBP_ID_4734159,Human_RBP_ID_5602254,Human_RBP_ID_9137182,Human_RBP_ID_18342157,Human_RBP_ID_18413413,Human_RBP_ID_26347529,Human_RBP_ID_26824326,Human_RBP_ID_27049836 55725 RMVar_ID_55725 Human_SNP_ID_166704822 m1A Human chr3 - 185418562 185418562 185418562 CCAGTGCTGAGTCTTGGGGTACTGGCAGAGCTATGGCTCGAATTCCCAGAGTTCGAGGTGGTGGG CCAGTGCTGAGTCTTGGGGTACTGGCAGAGCTGTGGCTCGAATTCCCAGAGTTCGAGGTGGTGGG T C RPL4P4 Ensembl:ENSG00000229638 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879070985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064073,Human_RBP_ID_27316202 Human_miRNA_ID_1857559,Human_miRNA_ID_1858345,Human_miRNA_ID_1886653 55726 RMVar_ID_55726 Human_SNP_ID_166725379 m1A Human chr3 + 185498938 185498935 185498938 TACAAGGCGAAGGTGCAGCCGGCGAAGACCAGAAGGAGGCCGAGAAGCGGGCGCATGTCGGCTCC TACAAGGCGAAGGTGCAGCCGGCGAAGACC___AGGAGGCCGAGAAGCGGGCGCATGTCGGCTCC CAGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:185498876..185499000 26863410 MeRIP-seq:(Medium) rs776994309 Functional Loss DEL dbSNP153 31..33 33 - - - 55727 RMVar_ID_55727 Human_SNP_ID_166725382 m1A Human chr3 + 185498938 185498938 185498938 TACAAGGCGAAGGTGCAGCCGGCGAAGACCAGAAGGAGGCCGAGAAGCGGGCGCATGTCGGCTCC TACAAGGCGAAGGTGCAGCCGGCGAAGACCAGTAGGAGGCCGAGAAGCGGGCGCATGTCGGCTCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:185498876..185499000 26863410 MeRIP-seq:(Medium) rs752135151 Functional Loss SNV dbSNP153 33..33 33 - - - 55728 RMVar_ID_55728 Human_SNP_ID_166760729 m1A Human chr3 - 185635447 185635447 185635447 GAAAGCAAAACCACAGGTAGGGGGGTTTCTGTACTGTTCCATTTTGCCTAAGTCTTGAAATCCCC GAAAGCAAAACCACAGGTAGGGGGGTTTCTGTGCTGTTCCATTTTGCCTAAGTCTTGAAATCCCC T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7613002 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6632,GWAS_ID_6633,GWAS_ID_6634,GWAS_ID_6635,GWAS_ID_6636,GWAS_ID_6637,GWAS_ID_6638 55729 RMVar_ID_55729 Human_SNP_ID_166764210 m1A Human chr3 + 185647619 185647619 185647619 CCCTCCTCCTCGTTTTCACTCCTGCCGCCAAGACTTGCTCATGCTGTTCCTACCCTTGGATTGTT CCCTCCTCCTCGTTTTCACTCCTGCCGCCAAGGCTTGCTCATGCTGTTCCTACCCTTGGATTGTT A G lnc-SENP2-1 RNACentral:URS00008B88AF lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:185647587..185647744 26863196 MeRIP-seq:(Medium) rs1482265555 Functional Loss SNV dbSNP153 33..33 33 - - - 55730 RMVar_ID_55730 Human_SNP_ID_166808090 m1A Human chr3 - 185824942 185824942 185824942 CGGGGAAGAGACGGATGATGAACAAGCTTTACATCGGGAACCTGAGCCCCGCCGTCACCGCCGAC CGGGGAAGAGACGGATGATGAACAAGCTTTACGTCGGGAACCTGAGCCCCGCCGTCACCGCCGAC T C IGF2BP2 Ensembl:ENSG00000073792 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:185824833..185825030 26863196 MeRIP-seq:(Medium) rs376662015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1623783,Human_RBP_ID_1958065,Human_RBP_ID_3700082,Human_RBP_ID_8567546,Human_RBP_ID_9333985,Human_RBP_ID_9395828,Human_RBP_ID_17402815,Human_RBP_ID_18424109,Human_RBP_ID_18804250,Human_RBP_ID_19013319,Human_RBP_ID_26771272 RMVar_hsa_circ_95113,RMVar_hsa_circ_223508,RMVar_hsa_circ_88866,RMVar_hsa_circ_223519 55731 RMVar_ID_55731 Human_SNP_ID_166808227 m1A Human chr3 + 185825212 185825212 185825212 GGCAGAGTCCCGGGCCGGGCGGCGGCGCGCGGACAAAGCGCTCTCTCTGCCTCCCTCTCTCTCCC GGCAGAGTCCCGGGCCGGGCGGCGGCGCGCGGGCAAAGCGCTCTCTCTGCCTCCCTCTCTCTCCC A G lnc-SENP2-2,lnc-SENP2-2:2,lnc-SENP2-2:3 RNACentral:URS0000D5748A,RNACentral:URS0000D5D432,RNACentral:URS0000D5CE50 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:185825162..185825349 26863196 MeRIP-seq:(Medium) rs1001933620 Functional Loss SNV dbSNP153 33..33 33 - - - 55732 RMVar_ID_55732 Human_SNP_ID_166808351 m1A Human chr3 - 185825561 185825561 185825561 CGCGGCTCCCCGTCGCCCCCTCGCGCGCTCCCACCCGCGCCCGGGGCGCGCCTTCCCCGCCCCGC CGCGGCTCCCCGTCGCCCCCTCGCGCGCTCCCCCCCGCGCCCGGGGCGCGCCTTCCCCGCCCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:185825529..185825686 26863196 MeRIP-seq:(Medium) rs993032308 Functional Loss SNV dbSNP153 33..33 33 - - - 55733 RMVar_ID_55733 Human_SNP_ID_166808373 m1A Human chr3 + 185825629 185825629 185825629 GTGGGAGGGAGAGGGGCTGCGAGTGAGCGCGGAGAGGGGTGTGCGCAAGGTGGACCGGATGTGAG GTGGGAGGGAGAGGGGCTGCGAGTGAGCGCGGGGAGGGGTGTGCGCAAGGTGGACCGGATGTGAG A G lnc-SENP2-2,lnc-SENP2-2:2,lnc-SENP2-2:3 RNACentral:URS0000D5748A,RNACentral:URS0000D5D432,RNACentral:URS0000D5CE50 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:185825482..185825963 26863196 MeRIP-seq:(Medium) rs1253798321 Functional Loss SNV dbSNP153 33..33 33 - - - 55734 RMVar_ID_55734 Human_SNP_ID_166808586 m1A Human chr3 + 185826249 185826249 185826249 GTTCAGCTCCAAAGCCAGGGTGGTGGGAGGCGAGGGTGGCTGGAAGCGGAGGAGCGCAGGCTGTG GTTCAGCTCCAAAGCCAGGGTGGTGGGAGGCGGGGGTGGCTGGAAGCGGAGGAGCGCAGGCTGTG A G lnc-SENP2-2,lnc-SENP2-2:2,lnc-SENP2-2:3,lnc-SENP2-2:4,lnc-SENP2-2:5 RNACentral:URS0000D5748A,RNACentral:URS0000D5D432,RNACentral:URS00009ADB74,RNACentral:URS0000D5CE50,RNACentral:URS00008C3923 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:185826046..185826407 26863196 MeRIP-seq:(Medium) rs904614123 Functional Loss SNV dbSNP153 33..33 33 - - - 55735 RMVar_ID_55735 Human_SNP_ID_166808698 m1A Human chr3 - 185826628 185826628 185826628 CACCCAAGGACACTCCCCGCACCCGCGCCCCAACGCCTTCACAAAACCCAACATATCCGCGATCA CACCCAAGGACACTCCCCGCACCCGCGCCCCAGCGCCTTCACAAAACCCAACATATCCGCGATCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:185826580..185826662 26863196 MeRIP-seq:(Medium) rs1305226379 Functional Loss SNV dbSNP153 33..33 33 - - - 55736 RMVar_ID_55736 Human_SNP_ID_166834923 m1A Human chr3 + 185925631 185925631 185925631 CCTTCGGGAGCTTCTTCTGGATCTAGACCTGCAAGACAAAGACCTCCTAAGGTTATGACTGAAAA CCTTCGGGAGCTTCTTCTGGATCTAGACCTGCGAGACAAAGACCTCCTAAGGTTATGACTGAAAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:185925626..185925650 26863196 MeRIP-seq:(Medium) rs370636250 Functional Loss SNV dbSNP153 33..33 33 - - - 55737 RMVar_ID_55737 Human_SNP_ID_166835281 m1A Human chr3 - 185926713 185926713 185926713 TCTACGTGTAGGAATCCCGTTCTGCTTCCAGAAGTGGAAGTGCTCACGGATCGGGGAAATCTGCA TCTACGTGTAGGAATCCCGTTCTGCTTCCAGACGTGGAAGTGCTCACGGATCGGGGAAATCTGCA T G TRA2B Ensembl:ENSG00000136527 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:185926662..185926767 26863196 MeRIP-seq:(Medium) rs1439992730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67648,Human_RBP_ID_247346,Human_RBP_ID_938559,Human_RBP_ID_1623928,Human_RBP_ID_1958130,Human_RBP_ID_7170668,Human_RBP_ID_17149450,Human_RBP_ID_25763444 Human_Splice_Rec_520292,Human_Splice_Rec_520358,Human_Splice_Rec_520376,Human_Splice_Rec_520412,Human_Splice_Rec_520418,Human_Splice_Rec_520426 RMVar_hsa_circ_24186,RMVar_hsa_circ_1843,RMVar_hsa_circ_58615,RMVar_hsa_circ_62107,RMVar_hsa_circ_223528,RMVar_hsa_circ_374750,RMVar_hsa_circ_36738,RMVar_hsa_circ_22106,RMVar_hsa_circ_323822,RMVar_hsa_circ_223532 55738 RMVar_ID_55738 Human_SNP_ID_166838761 m1A Human chr3 - 185937874 185937874 185937874 GCAGCTTCGATTGAAGCACATCGACCGGCGACAGCAGCCAGGAGTCATGAGCGACAGCGGCGAGC GCAGCTTCGATTGAAGCACATCGACCGGCGACGGCAGCCAGGAGTCATGAGCGACAGCGGCGAGC T C TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr3:185937767..185938025;chr3:185937746..185938000 26863196 MeRIP-seq:(Medium) rs761114014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67650,Human_RBP_ID_247350,Human_RBP_ID_1623977,Human_RBP_ID_1958213,Human_RBP_ID_3700206,Human_RBP_ID_4734526,Human_RBP_ID_7170977,Human_RBP_ID_9334388,Human_RBP_ID_9395831,Human_RBP_ID_14752530,Human_RBP_ID_18424110,Human_RBP_ID_22822933,Human_RBP_ID_23026566,Human_RBP_ID_23990667,Human_RBP_ID_24382401,Human_RBP_ID_26346380,Human_RBP_ID_27049995 Human_Splice_Rec_520291,Human_Splice_Rec_520373,Human_Splice_Rec_520391,Human_Splice_Rec_520405,Human_Splice_Rec_520411,Human_Splice_Rec_520427,Human_Splice_Rec_520429 Human_miRNA_ID_2330650,Human_miRNA_ID_2330651,Human_miRNA_ID_2963732,Human_miRNA_ID_2963733 RMVar_hsa_circ_116021,RMVar_hsa_circ_108800,RMVar_hsa_circ_223533,RMVar_hsa_circ_223534 55739 RMVar_ID_55739 Human_SNP_ID_166838828 m1A Human chr3 - 185937963 185937963 185937963 TGCGGAGCATTTCGGCTCTGAGCGGCTGGGCGACCGGCGCGTCGTGCGGGGCTGCGGCGGAGCCT TGCGGAGCATTTCGGCTCTGAGCGGCTGGGCGGCCGGCGCGTCGTGCGGGGCTGCGGCGGAGCCT T C TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:185937730..185938082;chr3:185937757..185938058 26863196 MeRIP-seq:(Medium) rs1045451749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247351,Human_RBP_ID_783383,Human_RBP_ID_836167,Human_RBP_ID_938563,Human_RBP_ID_1623979,Human_RBP_ID_4734527,Human_RBP_ID_5325757,Human_RBP_ID_5425196,Human_RBP_ID_5474046,Human_RBP_ID_5505979,Human_RBP_ID_8870402,Human_RBP_ID_8943593,Human_RBP_ID_9333986,Human_RBP_ID_14752532,Human_RBP_ID_18424111,Human_RBP_ID_18804365,Human_RBP_ID_22092062,Human_RBP_ID_22278932,Human_RBP_ID_22457605,Human_RBP_ID_23026566,Human_RBP_ID_23135075,Human_RBP_ID_26346381 RMVar_hsa_circ_116021,RMVar_hsa_circ_223534 55740 RMVar_ID_55740 Human_SNP_ID_166838834 m1A Human chr3 + 185937969 185937969 185937969 CGCCGCAGCCCCGCACGACGCGCCGGTCGCCCAGCCGCTCAGAGCCGAAATGCTCCGCACCGCCT CGCCGCAGCCCCGCACGACGCGCCGGTCGCCCGGCCGCTCAGAGCCGAAATGCTCCGCACCGCCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr3:185937826..185938025;chr3:185937736..185938086 26863196 MeRIP-seq:(Medium) rs1349956596 Functional Loss SNV dbSNP153 33..33 33 - - - 55741 RMVar_ID_55741 Human_SNP_ID_166838841 m1A Human chr3 - 185937975 185937975 185937975 GTGCGGAGGCGGTGCGGAGCATTTCGGCTCTGAGCGGCTGGGCGACCGGCGCGTCGTGCGGGGCT GTGCGGAGGCGGTGCGGAGCATTTCGGCTCTGGGCGGCTGGGCGACCGGCGCGTCGTGCGGGGCT T C TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr3:185937951..185938000;chr3:185937951..185937975 26863196,32194978 MeRIP-seq:(Medium) rs1046519704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783383,Human_RBP_ID_836167,Human_RBP_ID_938563,Human_RBP_ID_1623980,Human_RBP_ID_4734527,Human_RBP_ID_5325757,Human_RBP_ID_5425196,Human_RBP_ID_5505979,Human_RBP_ID_8870403,Human_RBP_ID_8943593,Human_RBP_ID_9333986,Human_RBP_ID_14752532,Human_RBP_ID_18424111,Human_RBP_ID_18446356,Human_RBP_ID_18804365,Human_RBP_ID_22092062,Human_RBP_ID_22457605,Human_RBP_ID_23026566,Human_RBP_ID_23135075,Human_RBP_ID_26346381 RMVar_hsa_circ_116021,RMVar_hsa_circ_223534 55742 RMVar_ID_55742 Human_SNP_ID_166994244 m1A Human chr3 + 186570839 186570818 186570839 GGCCTCACAGGGCCGGGTGGGCTGGCGAGCCGACGCGGCGGCGGAGGAGGCTGTGAGGAGTGTGT GGCCTCACAGGG_____________________CGCGGCGGCGGAGGAGGCTGTGAGGAGTGTGT GCCGGGTGGGCTGGCGAGCCGA G DNAJB11 Ensembl:ENSG00000090520 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:186570751..186570925 26863410 MeRIP-seq:(Medium) rs1176256686 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_1311758,Human_RBP_ID_4734606,Human_RBP_ID_9394435,Human_RBP_ID_17661619,Human_RBP_ID_18471755,Human_RBP_ID_22456357,Human_RBP_ID_24547597,Human_RBP_ID_26347546 RMVar_hsa_circ_86211,RMVar_hsa_circ_223561 55743 RMVar_ID_55743 Human_SNP_ID_167049429 m1A Human chr3 + 186783638 186783638 186783638 GGATCATGTCTGGTGGCTCCGCGGATTATAACAGGTATGCAGTCTGTTGGCGGTCGCGGTCTGTA GGATCATGTCTGGTGGCTCCGCGGATTATAACGGGTATGCAGTCTGTTGGCGGTCGCGGTCTGTA A G EIF4A2 Ensembl:ENSG00000156976 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr3:186783621..186783768;chr3:186783578..186783829 26863196,32194978 MeRIP-seq:(Medium) rs1317806581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934093,Human_RBP_ID_1032391,Human_RBP_ID_2771983,Human_RBP_ID_4757624,Human_RBP_ID_5506001,Human_RBP_ID_18424113,Human_RBP_ID_18446362,Human_RBP_ID_18804413,Human_RBP_ID_19013331,Human_RBP_ID_19119108,Human_RBP_ID_22092063,Human_RBP_ID_23021344,Human_RBP_ID_23213334 Human_Splice_Rec_521737,Human_Splice_Rec_521741,Human_Splice_Rec_521747,Human_Splice_Rec_521765,Human_Splice_Rec_521767,Human_Splice_Rec_521769,Human_Splice_Rec_521773,Human_Splice_Rec_521779,Human_Splice_Rec_521785,Human_Splice_Rec_521791,Human_Splice_Rec_521809,Human_Splice_Rec_521831,Human_Splice_Rec_521851,Human_Splice_Rec_521871,Human_Splice_Rec_521877,Human_Splice_Rec_521889 RMVar_hsa_circ_85571,RMVar_hsa_circ_223573 55744 RMVar_ID_55744 Human_SNP_ID_167049675 m1A Human chr3 + 186784080 186784080 186784080 TCCACTCGGCCACGGCGCGGAGGCGACGGGACAGGACCGGTGCCGGTGAACCGTTGGCATCGCCC TCCACTCGGCCACGGCGCGGAGGCGACGGGACCGGACCGGTGCCGGTGAACCGTTGGCATCGCCC A C EIF4A2 Ensembl:ENSG00000156976 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186784078..186784179 32194978 MeRIP-seq:(Medium) rs918178217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85571,RMVar_hsa_circ_223573 55745 RMVar_ID_55745 Human_SNP_ID_167049676 m1A Human chr3 + 186784080 186784080 186784080 TCCACTCGGCCACGGCGCGGAGGCGACGGGACAGGACCGGTGCCGGTGAACCGTTGGCATCGCCC TCCACTCGGCCACGGCGCGGAGGCGACGGGACGGGACCGGTGCCGGTGAACCGTTGGCATCGCCC A G EIF4A2 Ensembl:ENSG00000156976 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186784078..186784179 32194978 MeRIP-seq:(Medium) rs918178217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85571,RMVar_hsa_circ_223573 55746 RMVar_ID_55746 Human_SNP_ID_167049720 m1A Human chr3 + 186784141 186784141 186784141 GCCCTCGCCAGGCCGCTCCGCCCGCGTCAATCACCCGGCTTGCGCATTGTTGGGGGCGGAGTTCG GCCCTCGCCAGGCCGCTCCGCCCGCGTCAATCGCCCGGCTTGCGCATTGTTGGGGGCGGAGTTCG A G EIF4A2 Ensembl:ENSG00000156976 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:186784037..186784330 26863196 MeRIP-seq:(Medium) rs1213896909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85571,RMVar_hsa_circ_223573 55747 RMVar_ID_55747 Human_SNP_ID_167049764 m1A Human chr3 + 186784221 186784221 186784221 GCGAGACGCTCCGCAGTTGAAACGGGATCGCCATGCGCTCGGGCCTGGGGGGCTGCCTTTCCGGG GCGAGACGCTCCGCAGTTGAAACGGGATCGCCGTGCGCTCGGGCCTGGGGGGCTGCCTTTCCGGG A G EIF4A2 Ensembl:ENSG00000156976 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186784216..186784316 32194978 MeRIP-seq:(Medium) rs912262200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7171376 RMVar_hsa_circ_85571,RMVar_hsa_circ_223573 55748 RMVar_ID_55748 Human_SNP_ID_167049883 m1A Human chr3 + 186784447 186784447 186784447 AGTATTCTTGTCAGCAGAGAACATGGCGGCCCAGAGGGAATGGACCCCGATGGTGTCATCGAGGT AGTATTCTTGTCAGCAGAGAACATGGCGGCCCGGAGGGAATGGACCCCGATGGTGTCATCGAGGT A G EIF4A2 Ensembl:ENSG00000156976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:186784406..186784574 26863196 MeRIP-seq:(Medium) rs1369398487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68086,Human_RBP_ID_247455,Human_RBP_ID_597117,Human_RBP_ID_835898,Human_RBP_ID_933485,Human_RBP_ID_4734669,Human_RBP_ID_5393859,Human_RBP_ID_14752930,Human_RBP_ID_19011225,Human_RBP_ID_19116484,Human_RBP_ID_22480714,Human_RBP_ID_22609233,Human_RBP_ID_22676963,Human_RBP_ID_23026567,Human_RBP_ID_26790951,Human_RBP_ID_27822810 Human_Splice_Rec_521738,Human_Splice_Rec_521739,Human_Splice_Rec_521742,Human_Splice_Rec_521743,Human_Splice_Rec_521748,Human_Splice_Rec_521749,Human_Splice_Rec_521766,Human_Splice_Rec_521768,Human_Splice_Rec_521770,Human_Splice_Rec_521771,Human_Splice_Rec_521774,Human_Splice_Rec_521775,Human_Splice_Rec_521780,Human_Splice_Rec_521781,Human_Splice_Rec_521786,Human_Splice_Rec_521787,Human_Splice_Rec_521792,Human_Splice_Rec_521793,Human_Splice_Rec_521810,Human_Splice_Rec_521811,Human_Splice_Rec_521832,Human_Splice_Rec_521833,Human_Splice_Rec_521852,Human_Splice_Rec_521853,Human_Splice_Rec_521872,Human_Splice_Rec_521873,Human_Splice_Rec_521878,Human_Splice_Rec_521879,Human_Splice_Rec_521890,Human_Splice_Rec_521891,Human_Splice_Rec_521907,Human_Splice_Rec_521913 Human_miRNA_ID_2423517,Human_miRNA_ID_2433176,Human_miRNA_ID_2955207 RMVar_hsa_circ_122792,RMVar_hsa_circ_85571,RMVar_hsa_circ_223573,RMVar_hsa_circ_223574 55749 RMVar_ID_55749 Human_SNP_ID_167050492 m1A Human chr3 + 186785962 186785962 186785962 TCATGCCTGCATTGGTGGAACAAATGTTCGAAATGAAATGCAAAAACTGCAGGCTGAAGCACCAC TCATGCCTGCATTGGTGGAACAAATGTTCGAAGTGAAATGCAAAAACTGCAGGCTGAAGCACCAC A G EIF4A2 Ensembl:ENSG00000156976 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186785911..186786011 32194978 MeRIP-seq:(Medium) rs758037831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1624029,Human_RBP_ID_1958270,Human_RBP_ID_3700277,Human_RBP_ID_9137419,Human_RBP_ID_14753023,Human_RBP_ID_18013998,Human_RBP_ID_18804426,Human_RBP_ID_23990814,Human_RBP_ID_26824341 Human_Splice_Rec_521752,Human_Splice_Rec_521753,Human_Splice_Rec_521790,Human_Splice_Rec_521796,Human_Splice_Rec_521797,Human_Splice_Rec_521816,Human_Splice_Rec_521817,Human_Splice_Rec_521838,Human_Splice_Rec_521839,Human_Splice_Rec_521858,Human_Splice_Rec_521859,Human_Splice_Rec_521875,Human_Splice_Rec_521882,Human_Splice_Rec_521883,Human_Splice_Rec_521894,Human_Splice_Rec_521895,Human_Splice_Rec_521912,Human_Splice_Rec_521916,Human_Splice_Rec_521918,Human_Splice_Rec_521919,Human_Splice_Rec_521921,Human_Splice_Rec_521929 Human_miRNA_ID_185213,Human_miRNA_ID_2004437 RMVar_hsa_circ_31066,RMVar_hsa_circ_122792,RMVar_hsa_circ_57867,RMVar_hsa_circ_223574,RMVar_hsa_circ_341683,RMVar_hsa_circ_298549,RMVar_hsa_circ_58834,RMVar_hsa_circ_33851,RMVar_hsa_circ_100445,RMVar_hsa_circ_223576,RMVar_hsa_circ_42417,RMVar_hsa_circ_223577,RMVar_hsa_circ_27645,RMVar_hsa_circ_44752,RMVar_hsa_circ_343467,RMVar_hsa_circ_223578 55750 RMVar_ID_55750 Human_SNP_ID_167050745 m1A Human chr3 + 186786609 186786609 186786609 ATTCTGGTGAAAAAGGAAGAATTGACCCTTGAAGGAATCAAACAGTTTTATATTAATGTTGAGAG ATTCTGGTGAAAAAGGAAGAATTGACCCTTGAGGGAATCAAACAGTTTTATATTAATGTTGAGAG A G EIF4A2 Ensembl:ENSG00000156976 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186786559..186786709 32194978 MeRIP-seq:(Medium) rs1322992089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_597135,Human_RBP_ID_1624042,Human_RBP_ID_1958283,Human_RBP_ID_9137423,Human_RBP_ID_9394443,Human_RBP_ID_23990822 Human_Splice_Rec_521757,Human_Splice_Rec_521801,Human_Splice_Rec_521821,Human_Splice_Rec_521843,Human_Splice_Rec_521863,Human_Splice_Rec_521887,Human_Splice_Rec_521899,Human_Splice_Rec_521925,Human_Splice_Rec_521933,Human_Splice_Rec_521939,Human_Splice_Rec_521943 Human_miRNA_ID_153469,Human_miRNA_ID_549448,Human_miRNA_ID_1316440,Human_miRNA_ID_1344297,Human_miRNA_ID_2647159,Human_miRNA_ID_2669752,Human_miRNA_ID_3100400 RMVar_hsa_circ_122792,RMVar_hsa_circ_57867,RMVar_hsa_circ_223574,RMVar_hsa_circ_341683,RMVar_hsa_circ_100445,RMVar_hsa_circ_223577,RMVar_hsa_circ_27645,RMVar_hsa_circ_44752,RMVar_hsa_circ_343467,RMVar_hsa_circ_273582,RMVar_hsa_circ_118248,RMVar_hsa_circ_223578,RMVar_hsa_circ_223579,RMVar_hsa_circ_295507,RMVar_hsa_circ_223580,RMVar_hsa_circ_223581 55751 RMVar_ID_55751 Human_SNP_ID_167052211 m1A Human chr3 - 186789751 186789751 186789751 AGGGTCCAGTTCACACTTAGCACTAATTAAATACTTTATTGAATAAATACAATACCAAACAAAAT AGGGTCCAGTTCACACTTAGCACTAATTAAATGCTTTATTGAATAAATACAATACCAAACAAAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186789550..186789750 32194978 MeRIP-seq:(Medium) rs935330751 Functional Loss SNV dbSNP153 33..33 33 - - - 55752 RMVar_ID_55752 Human_SNP_ID_167052628 m1A Human chr3 - 186790228 186790228 186790228 TATAGGATTTAATAGATGAGGGTCATGCAGCAACTCAGCTCGTCAATCAACTCCATGATGTGGTT TATAGGATTTAATAGATGAGGGTCATGCAGCAGCTCAGCTCGTCAATCAACTCCATGATGTGGTT T C RFC4 Ensembl:ENSG00000163918 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186790179..186790279 32194978 MeRIP-seq:(Medium) rs775221292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032411,Human_RBP_ID_1624116,Human_RBP_ID_1958334,Human_RBP_ID_5390406,Human_RBP_ID_7171487,Human_RBP_ID_14753238,Human_RBP_ID_17518899,Human_RBP_ID_18804480,Human_RBP_ID_19120051,Human_RBP_ID_22509274,Human_RBP_ID_22825200,Human_RBP_ID_25764137 Human_Splice_Rec_521970,Human_Splice_Rec_521971,Human_Splice_Rec_521998,Human_Splice_Rec_521999,Human_Splice_Rec_522018,Human_Splice_Rec_522019,Human_Splice_Rec_522024,Human_Splice_Rec_522025 RMVar_hsa_circ_101375,RMVar_hsa_circ_223589,RMVar_hsa_circ_223588,RMVar_hsa_circ_283518 55753 RMVar_ID_55753 Human_SNP_ID_167056882 m1A Human chr3 + 186806312 186806312 186806312 AGCAGGTTACCAGTTAGCCTGGCTTCTCGTGCAGGTCACCGCCGCCGGCTCGTTCCTCAGGTTTC AGCAGGTTACCAGTTAGCCTGGCTTCTCGTGCTGGTCACCGCCGCCGGCTCGTTCCTCAGGTTTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186806306..186806407 32194978 MeRIP-seq:(Medium) rs1362577136 Functional Loss SNV dbSNP153 33..33 33 - - - 55754 RMVar_ID_55754 Human_SNP_ID_167062350 m1A Human chr3 + 186827331 186827331 186827331 GAGGGCGCGGCGCCCGAGGACCTCCACCCCGGAGAGCTGCCCTCCCTGCGGTCGCCCCGGCTCCC GAGGGCGCGGCGCCCGAGGACCTCCACCCCGGCGAGCTGCCCTCCCTGCGGTCGCCCCGGCTCCC A C AC112907.2 Ensembl:ENSG00000231982 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:186827258..186827355 26863196 MeRIP-seq:(Medium) rs1277392624 Functional Loss SNV dbSNP153 33..33 33 - - - 55755 RMVar_ID_55755 Human_SNP_ID_167141040 m1A Human chr3 - 187139449 187139449 187139449 GGCGCGCGGCGGTTGAATTGCTGCGCCCAGCGAGGCAACCGCCTCCGAACGCCAGGTGGGGGCGA GGCGCGCGGCGGTTGAATTGCTGCGCCCAGCGGGGCAACCGCCTCCGAACGCCAGGTGGGGGCGA T C RPL39L Ensembl:ENSG00000163923 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:187139226..187139500 26863196 MeRIP-seq:(Medium) rs1446855350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757633 55756 RMVar_ID_55756 Human_SNP_ID_167284709 m1A Human chr3 - 187721823 187721823 187721823 TGAGAAAGAGCACTTAAGAGAATATTTTAAGTATTGCATCTGTATAAGTAAGAAAATATTTTGTC TGAGAAAGAGCACTTAAGAGAATATTTTAAGTTTTGCATCTGTATAAGTAAGAAAATATTTTGTC T A BCL6 Ensembl:ENSG00000113916 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs115678349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8949904,Human_RBP_ID_23991033 Human_miRNA_ID_532903,Human_miRNA_ID_539109,Human_miRNA_ID_1255636 55757 RMVar_ID_55757 Human_SNP_ID_167285526 m1A Human chr3 - 187725399 187725399 187725399 GCAGGCAAGCGGAGGAGTGGGCAGGCAAGTGGAGCGGGCAGGCAAGCGGAGCGGGCAGGTGAGCA GCAGGCAAGCGGAGGAGTGGGCAGGCAAGTGGGGCGGGCAGGCAAGCGGAGCGGGCAGGTGAGCA T C BCL6 Ensembl:ENSG00000113916 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:187725244..187725482 26863196 MeRIP-seq:(Medium) rs1174732752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5392384,Human_RBP_ID_19116498,Human_RBP_ID_26790956 55758 RMVar_ID_55758 Human_SNP_ID_167286606 m1A Human chr3 - 187729370 187729370 187729370 CAGAAATCTGACTGCCAGCCCAACTCGCCCACAGAGTCCTGCAGCAGTAAGAATGCCTGCATCCT CAGAAATCTGACTGCCAGCCCAACTCGCCCACGGAGTCCTGCAGCAGTAAGAATGCCTGCATCCT T C BCL6 Ensembl:ENSG00000113916 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:187729320..187729489 26863196 MeRIP-seq:(Medium) rs1560150356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_169016 RMVar_hsa_circ_365430,RMVar_hsa_circ_57705 55759 RMVar_ID_55759 Human_SNP_ID_167288660 m1A Human chr3 - 187737559 187737559 187737559 GAGTGGTCGGGGTGGGGTAGCGAAGTCTGCCTAGGCTTGCCCCGGCGCGCAGGGCTGGTGTTTGT GAGTGGTCGGGGTGGGGTAGCGAAGTCTGCCTGGGCTTGCCCCGGCGCGCAGGGCTGGTGTTTGT T C BCL6 Ensembl:ENSG00000113916 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:187737526..187737672 26863196 MeRIP-seq:(Medium) rs1163929743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784968,Human_RBP_ID_3722286,Human_RBP_ID_5241639,Human_RBP_ID_8124673,Human_RBP_ID_17152334,Human_RBP_ID_17208852,Human_RBP_ID_17292563,Human_RBP_ID_17404818,Human_RBP_ID_18499863,Human_RBP_ID_20969437,Human_RBP_ID_22480839,Human_RBP_ID_23026418,Human_RBP_ID_24429150,Human_RBP_ID_24561416,Human_RBP_ID_26790228 55760 RMVar_ID_55760 Human_SNP_ID_167291343 m1A Human chr3 + 187745309 187745309 187745309 GCAAGAGCGGAAAAAAAAAGAATTAAAAGGTAAAATAATGATCATGAGCAGCGGCGGCGGCAGCG GCAAGAGCGGAAAAAAAAAGAATTAAAAGGTAGAATAATGATCATGAGCAGCGGCGGCGGCAGCG A G AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:187745307..187745413 26863196 MeRIP-seq:(Medium) rs573157591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_522554 55761 RMVar_ID_55761 Human_SNP_ID_167291361 m1A Human chr3 + 187745338 187745338 187745338 GTAAAATAATGATCATGAGCAGCGGCGGCGGCAGCGGCACCAGCGGCAACAGCGGCGGCGGCGGC GTAAAATAATGATCATGAGCAGCGGCGGCGGCGGCGGCACCAGCGGCAACAGCGGCGGCGGCGGC A G AC072022.2 Ensembl:ENSG00000285938 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:187745327..187745428 26863196 MeRIP-seq:(Medium) rs1342857303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_522554 55762 RMVar_ID_55762 Human_SNP_ID_167390358 m1A Human chr3 + 188136590 188136588 188136590 TGCACTCCAGCCTGGGCGAACTAGCTCTCAGAAAAAAAAAAAAAAAACATAAACAAAAACAAAGG TGCACTCCAGCCTGGGCGAACTAGCTCTCAG__AAAAAAAAAAAAAACATAAACAAAAACAAAGG GAA G AC022498.1 Ensembl:ENSG00000234238 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:188136520..188136638 26863410 MeRIP-seq:(Medium) rs62866760 Functional Loss DEL dbSNP153 32..33 33 - - - 55763 RMVar_ID_55763 Human_SNP_ID_167390359 m1A Human chr3 + 188136590 188136588 188136590 TGCACTCCAGCCTGGGCGAACTAGCTCTCAGAAAAAAAAAAAAAAAACATAAACAAAAACAAAGG TGCACTCCAGCCTGGGCGAACTAGCTCTCAGA_AAAAAAAAAAAAAACATAAACAAAAACAAAGG GAA GA AC022498.1 Ensembl:ENSG00000234238 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:188136520..188136638 26863410 MeRIP-seq:(Medium) rs62866760 Functional Loss DEL dbSNP153 33..33 33 - - - 55764 RMVar_ID_55764 Human_SNP_ID_167390365 m1A Human chr3 + 188136590 188136590 188136590 TGCACTCCAGCCTGGGCGAACTAGCTCTCAGAAAAAAAAAAAAAAAACATAAACAAAAACAAAGG TGCACTCCAGCCTGGGCGAACTAGCTCTCAGAGAAAAAAAAAAAAAACATAAACAAAAACAAAGG A G AC022498.1 Ensembl:ENSG00000234238 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:188136520..188136638 26863410 MeRIP-seq:(Medium) rs1251713703 Functional Loss SNV dbSNP153 33..33 33 - - - 55765 RMVar_ID_55765 Human_SNP_ID_167396532 m1A Human chr3 - 188158246 188158244 188158246 CTAAGTTTCTTCTAGCAAAGCACAGCCCTCCAAAGCCAGATTCCAGGAAAAGTCCCACCCACCAA CTAAGTTTCTTCTAGCAAAGCACAGCCCTCCA__GCCAGATTCCAGGAAAAGTCCCACCCACCAA CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:188158226..188158336 26863196 MeRIP-seq:(Medium) rs1343390721 Functional Loss DEL dbSNP153 33..34 33 - - - 55766 RMVar_ID_55766 Human_SNP_ID_167410694 m1A Human chr3 - 188217208 188217208 188217208 CTACAAGGTGGCCTCCTTGTCACTCAGATCTCAGCTTAAACATAACCTCCCAGAGTCCTTCCCCA CTACAAGGTGGCCTCCTTGTCACTCAGATCTCTGCTTAAACATAACCTCCCAGAGTCCTTCCCCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:188217200..188217374 26863196 MeRIP-seq:(Medium) rs114645357 Functional Loss SNV dbSNP153 33..33 33 - - - 55767 RMVar_ID_55767 Human_SNP_ID_167507353 m1A Human chr3 + 188609336 188609336 188609336 CCCTGTGGCTCCAATCGGAACACTCAAACCCCAGCCTCAGCCAGTCCCAGCCTCCTACACCACGG CCCTGTGGCTCCAATCGGAACACTCAAACCCCTGCCTCAGCCAGTCCCAGCCTCCTACACCACGG A T LPP Ensembl:ENSG00000145012 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:188609285..188609398 26863196 MeRIP-seq:(Medium) rs774281484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155089,Human_RBP_ID_18954850 Human_miRNA_ID_795085,Human_miRNA_ID_1359812,Human_miRNA_ID_1396950,Human_miRNA_ID_2330653,Human_miRNA_ID_2330654,Human_miRNA_ID_2683467,Human_miRNA_ID_2683468,Human_miRNA_ID_2713032,Human_miRNA_ID_2713033,Human_miRNA_ID_2713034,Human_miRNA_ID_2713035,Human_miRNA_ID_2963735,Human_miRNA_ID_2963736,Human_miRNA_ID_3049010,Human_miRNA_ID_3049011,Human_miRNA_ID_3049012,Human_miRNA_ID_3049013 RMVar_hsa_circ_41507,RMVar_hsa_circ_101572,RMVar_hsa_circ_223625,RMVar_hsa_circ_105937,RMVar_hsa_circ_223633,RMVar_hsa_circ_223628,RMVar_hsa_circ_319899,RMVar_hsa_circ_344020,RMVar_hsa_circ_223632,RMVar_hsa_circ_71006,RMVar_hsa_circ_223631,RMVar_hsa_circ_55780,RMVar_hsa_circ_311857,RMVar_hsa_circ_364750,RMVar_hsa_circ_223634,RMVar_hsa_circ_223638,RMVar_hsa_circ_286562,RMVar_hsa_circ_223637,RMVar_hsa_circ_338803,RMVar_hsa_circ_352269,RMVar_hsa_circ_338615,RMVar_hsa_circ_301000,RMVar_hsa_circ_223640,RMVar_hsa_circ_285376,RMVar_hsa_circ_223639 55768 RMVar_ID_55768 Human_SNP_ID_167922243 m1A Human chr3 - 190306314 190306314 190306314 GAGACAGTGAAGTAAAATTGAGTGCACTAAACAAATAAGATTCTGAGGAAGTCTTATCTTCTGCA GAGACAGTGAAGTAAAATTGAGTGCACTAAACGAATAAGATTCTGAGGAAGTCTTATCTTCTGCA T C CLDN1 Ensembl:ENSG00000163347 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1895708 Functional Loss SNV dbSNP153 33..33 33 - - - 55769 RMVar_ID_55769 Human_SNP_ID_167974823 m1A Human chr3 + 190514139 190514139 190514139 GGATCCAGGTCTCCGGGGTCCGCTTTGGCCAGAGGCGCGGAAGGAAGCAGTGCCCGGCGACACTG GGATCCAGGTCTCCGGGGTCCGCTTTGGCCAGCGGCGCGGAAGGAAGCAGTGCCCGGCGACACTG A C IL1RAP Ensembl:ENSG00000196083 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:190514016..190514196 26863196 MeRIP-seq:(Medium) rs914420535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756905 Human_Splice_Rec_523241,Human_Splice_Rec_523261,Human_Splice_Rec_523285,Human_Splice_Rec_523307,Human_Splice_Rec_523313,Human_Splice_Rec_523315,Human_Splice_Rec_523331,Human_Splice_Rec_523341,Human_Splice_Rec_523355,Human_Splice_Rec_523375,Human_Splice_Rec_523393,Human_Splice_Rec_523415,Human_Splice_Rec_523419 55770 RMVar_ID_55770 Human_SNP_ID_168433661 m1A Human chr3 - 192401629 192401629 192401629 TGATATCATGCGACTTGTATTTTTAATTGGGCACTTTGCCTTTGGAGAAGAGAATGGATAGCAAT TGATATCATGCGACTTGTATTTTTAATTGGGCGCTTTGCCTTTGGAGAAGAGAATGGATAGCAAT T C FGF12 Ensembl:ENSG00000114279 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:192401627..192401706 32194978 MeRIP-seq:(Medium) rs900015291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223673 55771 RMVar_ID_55771 Human_SNP_ID_168558696 m1A Human chr3 - 192917786 192917784 192917787 CCAACAAGGCAGCCTCCCTGGGCTGTAACAACAAGCCTGCGTTCCCGGAGCTGGATTTCAGGTCG CCAACAAGGCAGCCTCCCTGGGCTGTAACAA___GCCTGCGTTCCCGGAGCTGGATTTCAGGTCG CTTG C MB21D2 Ensembl:ENSG00000180611 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:192917736..192917825 26863196 MeRIP-seq:(Medium) rs766721740 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1624241,Human_RBP_ID_4735334 Human_miRNA_ID_1749428 55772 RMVar_ID_55772 Human_SNP_ID_168746927 m1A Human chr3 + 193694882 193694880 193694883 ATGGCCATTAGGTTCAGTCCTTGAAGATAAGAAACTTGTTCTCTGTTTGTTGTCTTATTTGTGGT ATGGCCATTAGGTTCAGTCCTTGAAGATAAG___CTTGTTCTCTGTTTGTTGTCTTATTTGTGGT GAAA G OPA1 Ensembl:ENSG00000198836 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs938020725 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17194602,Human_RBP_ID_23213350 Human_miRNA_ID_2733044 RMVar_hsa_circ_122247,RMVar_hsa_circ_223702 55773 RMVar_ID_55773 Human_SNP_ID_168857758 m1A Human chr3 + 194136215 194136215 194136215 ATCCCCCGTCTACCTCTCTCCTTGGTCCTGGAACAGCGCTACTGATCACCAAGTAGCCACAAAAT ATCCCCCGTCTACCTCTCTCCTTGGTCCTGGACCAGCGCTACTGATCACCAAGTAGCCACAAAAT A C HES1 Ensembl:ENSG00000114315 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:194136167..194136304 26863196 MeRIP-seq:(Medium) rs1409866331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247156,Human_RBP_ID_1624330,Human_RBP_ID_4735511,Human_RBP_ID_23026569 RMVar_hsa_circ_100695,RMVar_hsa_circ_223709,RMVar_hsa_circ_96316,RMVar_hsa_circ_223710 55774 RMVar_ID_55774 Human_SNP_ID_168857781 m1A Human chr3 + 194136285 194136283 194136285 AAACCCTCAGCACTTGCTCAGTAGTTTTGTGAAAGTCTCAAGTAAAAGAGACACAAACAAAAAAT AAACCCTCAGCACTTGCTCAGTAGTTTTGTG__AGTCTCAAGTAAAAGAGACACAAACAAAAAAT GAA G HES1 Ensembl:ENSG00000114315 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:194136189..194136285 26863410 MeRIP-seq:(Medium) rs1023005601 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3701043,Human_RBP_ID_4735515 RMVar_hsa_circ_100695,RMVar_hsa_circ_223709,RMVar_hsa_circ_96316,RMVar_hsa_circ_223710 55775 RMVar_ID_55775 Human_SNP_ID_168905586 m1A Human chr3 - 194322811 194322811 194322811 CTGAGACAGAGAGCTACAGTCGCGCCTGCCACATCTACCTCCCCAGCCATCCTACTCTCTATGCT CTGAGACAGAGAGCTACAGTCGCGCCTGCCACGTCTACCTCCCCAGCCATCCTACTCTCTATGCT T C LINC00887 Ensembl:ENSG00000214145 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:194322564..194322843 26863196 MeRIP-seq:(Medium) rs146217839 Functional Loss SNV dbSNP153 33..33 33 - - - 55776 RMVar_ID_55776 Human_SNP_ID_168906262 m1A Human chr3 + 194324973 194324973 194324973 CACACCACATACGCACACACACCACACACCCCACATAGACACACATACCATACACACACACCAGA CACACCACATACGCACACACACCACACACCCCCCATAGACACACATACCATACACACACACCAGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:194324923..194325114 26863196 MeRIP-seq:(Medium) rs1312807687 Functional Loss SNV dbSNP153 33..33 33 - - - 55777 RMVar_ID_55777 Human_SNP_ID_168948102 m1A Human chr3 + 194476526 194476526 194476526 AGGAATTTAGAAGTCACCTTCGAACTCTTCCTATCTCACACCTACATCCAACCGGCCACTCATCT AGGAATTTAGAAGTCACCTTCGAACTCTTCCTGTCTCACACCTACATCCAACCGGCCACTCATCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:194476524..194476654 26863196 MeRIP-seq:(Medium) rs1328086173 Functional Loss SNV dbSNP153 33..33 33 - - - 55778 RMVar_ID_55778 Human_SNP_ID_168950474 m1A Human chr3 - 194486287 194486287 194486287 TGGTAGTCAGAGCTTTCGGAAAGTCCTGTGGGAGGTGGAGGTCCTGTGGGCAGAGGCGTAGGGGT TGGTAGTCAGAGCTTTCGGAAAGTCCTGTGGGCGGTGGAGGTCCTGTGGGCAGAGGCGTAGGGGT T G ATP13A3 Ensembl:ENSG00000133657 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:194486285..194486723 26863196 MeRIP-seq:(Medium) rs1030287746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721028,Human_RBP_ID_5393879,Human_RBP_ID_7174591,Human_RBP_ID_8124683,Human_RBP_ID_8235862,Human_RBP_ID_9435517,Human_RBP_ID_17152353 55779 RMVar_ID_55779 Human_SNP_ID_168950560 m1A Human chr3 - 194486539 194486539 194486539 GCCCCGGTGAGCGGGGCGAGGGGCGGGTGGGCAGCGGCGCCGGGGGAGGTCGAGGAGGCGAATGG GCCCCGGTGAGCGGGGCGAGGGGCGGGTGGGCGGCGGCGCCGGGGGAGGTCGAGGAGGCGAATGG T C ATP13A3 Ensembl:ENSG00000133657 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:194486533..194486710 26863196 MeRIP-seq:(Medium) rs193048747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3722334,Human_RBP_ID_18954040,Human_RBP_ID_19119169,Human_RBP_ID_26790978 55780 RMVar_ID_55780 Human_SNP_ID_168977352 m1A Human chr3 - 194587124 194587124 194587124 ATGATGTAGTATGGGCTGTAGGGGTGGCAAAAAGGCTGAAAAGGAACCAGACTGGAGGCTGGTGA ATGATGTAGTATGGGCTGTAGGGGTGGCAAAAGGGCTGAAAAGGAACCAGACTGGAGGCTGGTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:194587075..194587192 26863196 MeRIP-seq:(Medium) rs1418192123 Functional Loss SNV dbSNP153 33..33 33 - - - 55781 RMVar_ID_55781 Human_SNP_ID_168990532 m1A Human chr3 - 194633116 194633116 194633116 GCCACCGCGTCTGCATCTCCTTCGGCCTGTGGATCTGCGCCTCCTCCTGCTGGATCGCCGCCCAC GCCACCGCGTCTGCATCTCCTTCGGCCTGTGGCTCTGCGCCTCCTCCTGCTGGATCGCCGCCCAC T G TMEM44 Ensembl:ENSG00000145014 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:194632971..194633117 32194978 MeRIP-seq:(Medium) rs1286434071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_526815,Human_Splice_Rec_526853,Human_Splice_Rec_526871,Human_Splice_Rec_526891,Human_Splice_Rec_526973 55782 RMVar_ID_55782 Human_SNP_ID_168990625 m1A Human chr3 + 194633258 194633255 194633258 GGCGCGCGGCGCGGGGCCGGGGACCTGGGCGCAGCCTCCCTCGCCGCGGGCAAGCCCCGAGCGCC GGCGCGCGGCGCGGGGCCGGGGACCTGGGC___GCCTCCCTCGCCGCGGGCAAGCCCCGAGCGCC CGCA C AC046143.1 Ensembl:ENSG00000229334 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:194633192..194633360 26863196 MeRIP-seq:(Medium) rs1553842839 Functional Loss DEL dbSNP153 31..33 33 - - - 55783 RMVar_ID_55783 Human_SNP_ID_168990640 m1A Human chr3 - 194633322 194633322 194633322 GTCGGTGCGCTCGGCCGGAGGCGCCGCGGCGGAACGGAACCCAGAGAAGGGCACGCGGGGCGGCG GTCGGTGCGCTCGGCCGGAGGCGCCGCGGCGGTACGGAACCCAGAGAAGGGCACGCGGGGCGGCG T A TMEM44 Ensembl:ENSG00000145014 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:194633275..194633396 26863196 MeRIP-seq:(Medium) rs1174794169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757645 55784 RMVar_ID_55784 Human_SNP_ID_169001275 m1A Human chr3 - 194672153 194672153 194672153 CTTCGTCCAGCGGTCGTGTTGCCATGGGCCGGAGGAGAGCCCCGGCCGGTGGGTCGCTGGGACGG CTTCGTCCAGCGGTCGTGTTGCCATGGGCCGGTGGAGAGCCCCGGCCGGTGGGTCGCTGGGACGG T A LSG1 Ensembl:ENSG00000041802 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:194672080..194672165 26863196 MeRIP-seq:(Medium) rs373009841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757647,Human_RBP_ID_9303180,Human_RBP_ID_18446401 Human_Splice_Rec_526983,Human_Splice_Rec_527031,Human_Splice_Rec_527045 RMVar_hsa_circ_123723,RMVar_hsa_circ_223755 55785 RMVar_ID_55785 Human_SNP_ID_169004562 m1A Human chr3 + 194686007 194686005 194686008 GGAGCTGGACACCGCCTCGGAGGGAAGAAATGAGGTAGCGGCGGTTCCCGGACCCGGCCATGCCC GGAGCTGGACACCGCCTCGGAGGGAAGAAAT___GTAGCGGCGGTTCCCGGACCCGGCCATGCCC TGAG T FAM43A Ensembl:ENSG00000185112 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:194685876..194686250 26863196 MeRIP-seq:(Medium) rs1214420059 Functional Loss DEL dbSNP153 32..34 33 - - - 55786 RMVar_ID_55786 Human_SNP_ID_169004841 m1A Human chr3 + 194686846 194686846 194686846 GCGCCCTCCGGAGATGCTGCCGTGGAAGAAGCACAAGTTCGAGCTGCTGGCCGAGGCGCCGCCGC GCGCCCTCCGGAGATGCTGCCGTGGAAGAAGCGCAAGTTCGAGCTGCTGGCCGAGGCGCCGCCGC A G FAM43A Ensembl:ENSG00000185112 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:194686738..194686875 26863196 MeRIP-seq:(Medium) rs748055430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18804914 55787 RMVar_ID_55787 Human_SNP_ID_169005190 m1A Human chr3 + 194687674 194687674 194687674 GGAGCAACCCGAGGGCTGCCCGGAGGAGGAGGAGAACCGTGCGGCAGAGGGAGATCCAGCAGAGG GGAGCAACCCGAGGGCTGCCCGGAGGAGGAGGGGAACCGTGCGGCAGAGGGAGATCCAGCAGAGG A G FAM43A Ensembl:ENSG00000185112 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:194687571..194687800;chr3:194687588..194687777;chr3:194687595..194687808 26863196 MeRIP-seq:(Medium) rs1360986111 Functional Loss SNV dbSNP153 33..33 33 - - - 55788 RMVar_ID_55788 Human_SNP_ID_169005191 m1A Human chr3 + 194687676 194687676 194687676 AGCAACCCGAGGGCTGCCCGGAGGAGGAGGAGAACCGTGCGGCAGAGGGAGATCCAGCAGAGGAG AGCAACCCGAGGGCTGCCCGGAGGAGGAGGAGCACCGTGCGGCAGAGGGAGATCCAGCAGAGGAG A C FAM43A Ensembl:ENSG00000185112 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:194687625..194687881 26863196 MeRIP-seq:(Medium) rs1202481534 Functional Loss SNV dbSNP153 33..33 33 - - - 55789 RMVar_ID_55789 Human_SNP_ID_178435483 m1A Human chr4 + 30339912 30339912 30339912 TGTGTGAGTGTGCGTGTGAGTGTGTGCGTGAGAGTGTGTATGAGTGTGTGTGTGTGAGAGTGTGA TGTGTGAGTGTGCGTGTGAGTGTGTGCGTGAGTGTGTGTATGAGTGTGTGTGTGTGAGAGTGTGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:30339882..30339951 26863196 MeRIP-seq:(Medium) rs1158617753 Functional Loss SNV dbSNP153 33..33 33 - - - 55790 RMVar_ID_55790 Human_SNP_ID_178877851 m1A Human chr4 + 31997641 31997641 31997641 CCGCAGCTTCACTCTTGAGCCAGAGACCACGAACCCACCAGAAGGAAGAAACTCCAAACACATCC CCGCAGCTTCACTCTTGAGCCAGAGACCACGAGCCCACCAGAAGGAAGAAACTCCAAACACATCC A G LINC02506 Ensembl:ENSG00000251129 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:31997556..31997643 26863410 MeRIP-seq:(Medium) rs1286873717 Functional Loss SNV dbSNP153 33..33 33 - - - 55791 RMVar_ID_55791 Human_SNP_ID_180002265 m1A Human chr4 - 36244322 36244322 36244322 GCCGCCGCCAGGCAGCAGAGGCGACTGCGGACAGCCGGCGGGGACCGGGAAAGAGGAGGCCTGGC GCCGCCGCCAGGCAGCAGAGGCGACTGCGGACCGCCGGCGGGGACCGGGAAAGAGGAGGCCTGGC T G ARAP2 Ensembl:ENSG00000047365 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:36244273..36244369 26863196 MeRIP-seq:(Medium) rs374369070 Functional Loss SNV dbSNP153 33..33 33 - - - 55792 RMVar_ID_55792 Human_SNP_ID_180424246 m1A Human chr4 - 37977501 37977495 37977502 CTACCTTGGCCACCCAGCTGAACAATGGTGACATCGCGGGCCGGGCGGCGGCTCTTCGCCCGCCG CTACCTTGGCCACCCAGCTGAACAATGGTGA_______GGCCGGGCGGCGGCTCTTCGCCCGCCG CCGCGATG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:37977371..37977588 26863196 MeRIP-seq:(Medium) rs1344508395 Functional Loss DEL dbSNP153 32..38 33 - - - 55793 RMVar_ID_55793 Human_SNP_ID_180424250 m1A Human chr4 - 37977501 37977501 37977501 CTACCTTGGCCACCCAGCTGAACAATGGTGACATCGCGGGCCGGGCGGCGGCTCTTCGCCCGCCG CTACCTTGGCCACCCAGCTGAACAATGGTGACCTCGCGGGCCGGGCGGCGGCTCTTCGCCCGCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:37977371..37977588 26863196 MeRIP-seq:(Medium) rs1171954284 Functional Loss SNV dbSNP153 33..33 33 - - - 55794 RMVar_ID_55794 Human_SNP_ID_180432963 m1A Human chr4 - 38014655 38014655 38014655 TTCTCGATGCACTCGTCGATCAGGGCCGGCGGAGCCTTCTTGTGCGCCACCGTCACGCGGCCGCA TTCTCGATGCACTCGTCGATCAGGGCCGGCGGTGCCTTCTTGTGCGCCACCGTCACGCGGCCGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:38014606..38014712 26863196 MeRIP-seq:(Medium) rs1040392038 Functional Loss SNV dbSNP153 33..33 33 - - - 55795 RMVar_ID_55795 Human_SNP_ID_180432964 m1A Human chr4 - 38014655 38014655 38014655 TTCTCGATGCACTCGTCGATCAGGGCCGGCGGAGCCTTCTTGTGCGCCACCGTCACGCGGCCGCA TTCTCGATGCACTCGTCGATCAGGGCCGGCGGGGCCTTCTTGTGCGCCACCGTCACGCGGCCGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:38014606..38014712 26863196 MeRIP-seq:(Medium) rs1040392038 Functional Loss SNV dbSNP153 33..33 33 - - - 55796 RMVar_ID_55796 Human_SNP_ID_180462797 m1A Human chr4 + 38137377 38137377 38137377 AGGAGAGATTGCAACACCATCCCACACTGTCCAGGCCTTAACTGAGAGGGACAGAAGACGCTGGA AGGAGAGATTGCAACACCATCCCACACTGTCCGGGCCTTAACTGAGAGGGACAGAAGACGCTGGA A G TBC1D1 Ensembl:ENSG00000065882 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:38137326..38137425 32194978 MeRIP-seq:(Medium) rs962532185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267437 55797 RMVar_ID_55797 Human_SNP_ID_180586994 m1A Human chr4 + 38664262 38664262 38664262 CCGGAGTTGGTGCCAGGAGCCAGAGGGGAGCCAGGAGCGGAGCCGCGCGGAGCCGGGGCCCGAGC CCGGAGTTGGTGCCAGGAGCCAGAGGGGAGCCTGGAGCGGAGCCGCGCGGAGCCGGGGCCCGAGC A T KLF3 Ensembl:ENSG00000109787 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:38664142..38664461 26863196 MeRIP-seq:(Medium) rs1014923029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837874,Human_RBP_ID_4784676,Human_RBP_ID_9334665,Human_RBP_ID_18424568,Human_RBP_ID_22095473,Human_RBP_ID_26771442 Human_miRNA_ID_2082646 RMVar_hsa_circ_78058,RMVar_hsa_circ_225372 55798 RMVar_ID_55798 Human_SNP_ID_180587066 m1A Human chr4 + 38664412 38664412 38664412 TTGCTGCGCTCGGGGGGCTCCAGGCAGCCCGTATCGGGGCCTTTATTTCTCGTCGGCGGCGCCCT TTGCTGCGCTCGGGGGGCTCCAGGCAGCCCGTGTCGGGGCCTTTATTTCTCGTCGGCGGCGCCCT A G KLF3 Ensembl:ENSG00000109787 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:38664269..38664419 32194978 MeRIP-seq:(Medium) rs926487900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150620,Human_RBP_ID_22095474 Human_Splice_Rec_553937,Human_Splice_Rec_553943,Human_Splice_Rec_553953 RMVar_hsa_circ_78058,RMVar_hsa_circ_225372 55799 RMVar_ID_55799 Human_SNP_ID_180587067 m1A Human chr4 + 38664412 38664412 38664412 TTGCTGCGCTCGGGGGGCTCCAGGCAGCCCGTATCGGGGCCTTTATTTCTCGTCGGCGGCGCCCT TTGCTGCGCTCGGGGGGCTCCAGGCAGCCCGTTTCGGGGCCTTTATTTCTCGTCGGCGGCGCCCT A T KLF3 Ensembl:ENSG00000109787 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:38664269..38664419 32194978 MeRIP-seq:(Medium) rs926487900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150620,Human_RBP_ID_22095474 Human_Splice_Rec_553937,Human_Splice_Rec_553943,Human_Splice_Rec_553953 RMVar_hsa_circ_78058,RMVar_hsa_circ_225372 55800 RMVar_ID_55800 Human_SNP_ID_180589597 m1A Human chr4 + 38674583 38674583 38674583 GATGGTGTGTTAGTGTATTGCTCCGTATGCCTAGCCGAGGTCAGCTGGGAGACGGAAGTTTGCTT GATGGTGTGTTAGTGTATTGCTCCGTATGCCTCGCCGAGGTCAGCTGGGAGACGGAAGTTTGCTT A C KLF3 Ensembl:ENSG00000109787 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:38674580..38674668 26863196 MeRIP-seq:(Medium) rs967044419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78058,RMVar_hsa_circ_225372 55801 RMVar_ID_55801 Human_SNP_ID_180648778 m1A Human chr4 - 38910568 38910568 38910568 ATTTCTGATTCCTCATCACCTCTTCCTGTTCTACTTTGTCTTTTTCCCCATGGCACTCGCTCGTC ATTTCTGATTCCTCATCACCTCTTCCTGTTCTGCTTTGTCTTTTTCCCCATGGCACTCGCTCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:38910566..38910678 26863196 MeRIP-seq:(Medium) rs1269215979 Functional Loss SNV dbSNP153 33..33 33 - - - 55802 RMVar_ID_55802 Human_SNP_ID_180653921 m1A Human chr4 + 38931534 38931533 38931535 GTAGATGTGGCAAAAGTGTCCGAAGAAGAAACAAAGAAGGAAGAAAAGGAAGAGAAATCTCAAGA GTAGATGTGGCAAAAGTGTCCGAAGAAGAAAC__AGAAGGAAGAAAAGGAAGAGAAATCTCAAGA CAA C FAM114A1 Ensembl:ENSG00000197712 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:38931483..38931605 26863196 MeRIP-seq:(Medium) rs755131069 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9396252,Human_RBP_ID_24547657,Human_RBP_ID_26349949 Human_Splice_Rec_554054,Human_Splice_Rec_554055,Human_Splice_Rec_554082,Human_Splice_Rec_554083,Human_Splice_Rec_554096,Human_Splice_Rec_554097 RMVar_hsa_circ_4204,RMVar_hsa_circ_72043,RMVar_hsa_circ_361186,RMVar_hsa_circ_69362,RMVar_hsa_circ_367600,RMVar_hsa_circ_359088,RMVar_hsa_circ_57513,RMVar_hsa_circ_357976,RMVar_hsa_circ_365247,RMVar_hsa_circ_377198,RMVar_hsa_circ_350454,RMVar_hsa_circ_359157 55803 RMVar_ID_55803 Human_SNP_ID_180657289 m1A Human chr4 + 38944865 38944865 38944865 CCCGAGTCCGTGAAAAAATTGTCTTCCATGAAACCGGTCCCTGGTACCAGAAAGGTTGGGGACCA CCCGAGTCCGTGAAAAAATTGTCTTCCATGAAGCCGGTCCCTGGTACCAGAAAGGTTGGGGACCA A G FAM114A1 Ensembl:ENSG00000197712 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:38944844..38944944 32194978 MeRIP-seq:(Medium) rs1139089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212345 RMVar_hsa_circ_125537,RMVar_hsa_circ_225384 55804 RMVar_ID_55804 Human_SNP_ID_180657395 m1A Human chr4 + 38945279 38945279 38945279 GCTAAAGGACAGAAAATACTGATGTGTGTTTTAACTAACTGGTATATTGATCCATGGGAGGCTGC GCTAAAGGACAGAAAATACTGATGTGTGTTTTGACTAACTGGTATATTGATCCATGGGAGGCTGC A G FAM114A1 Ensembl:ENSG00000197712 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:38945042..38945292 32194978 MeRIP-seq:(Medium) rs1289397511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_153750 RMVar_hsa_circ_125537,RMVar_hsa_circ_225384 55805 RMVar_ID_55805 Human_SNP_ID_180682368 m1A Human chr4 - 39044952 39044952 39044952 CGCGCGCCCCTAGACCCTGTCCGGGCAGCCTCATCCCCGGCGCCGGCCGGCCCGGAGCGAGCCAC CGCGCGCCCCTAGACCCTGTCCGGGCAGCCTCGTCCCCGGCGCCGGCCGGCCCGGAGCGAGCCAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:39044851..39045050 26863410 MeRIP-seq:(Medium) rs1327362131 Functional Loss SNV dbSNP153 33..33 33 - - - 55806 RMVar_ID_55806 Human_SNP_ID_180682452 m1A Human chr4 + 39045072 39045072 39045072 TCCCGCCTGGCCGCCCCGGCCCGCCGTGACCCACGGCCGCCTCCGGAGCCCGACGCGGTAAGTGC TCCCGCCTGGCCGCCCCGGCCCGCCGTGACCCTCGGCCGCCTCCGGAGCCCGACGCGGTAAGTGC A T KLHL5 Ensembl:ENSG00000109790 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:39044729..39045128 26863196 MeRIP-seq:(Medium) rs1170535105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_554133,Human_Splice_Rec_554155 55807 RMVar_ID_55807 Human_SNP_ID_180742031 m1A Human chr4 + 39308876 39308876 39308876 CACCTGCTCCTTGAAATCCAGGCTTTTCCAAAACACATCTGTTTCCTTTTTTATTGTCTTTGCCA CACCTGCTCCTTGAAATCCAGGCTTTTCCAAAGCACATCTGTTTCCTTTTTTATTGTCTTTGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:39308826..39308909 26863196 MeRIP-seq:(Medium) rs1301779593 Functional Loss SNV dbSNP153 33..33 33 - - - 55808 RMVar_ID_55808 Human_SNP_ID_180743549 m1A Human chr4 - 39315701 39315701 39315701 ACTTGGTGATAATTGAAGTGGAAAGTGAGAAGAAAGAGTATTGGGGATGATCTTGTTATTGGCAT ACTTGGTGATAATTGAAGTGGAAAGTGAGAAGGAAGAGTATTGGGGATGATCTTGTTATTGGCAT T C RFC1 Ensembl:ENSG00000035928 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:39315683..39315758 26863196 MeRIP-seq:(Medium) rs144094949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87174,RMVar_hsa_circ_225414,RMVar_hsa_circ_43060,RMVar_hsa_circ_225415,RMVar_hsa_circ_124565,RMVar_hsa_circ_39863,RMVar_hsa_circ_104833,RMVar_hsa_circ_225417,RMVar_hsa_circ_67852,RMVar_hsa_circ_225420,RMVar_hsa_circ_71706,RMVar_hsa_circ_57704,RMVar_hsa_circ_32529,RMVar_hsa_circ_225424,RMVar_hsa_circ_342185,RMVar_hsa_circ_338414,RMVar_hsa_circ_317600,RMVar_hsa_circ_225422,RMVar_hsa_circ_225423,RMVar_hsa_circ_73796,RMVar_hsa_circ_81845,RMVar_hsa_circ_324193,RMVar_hsa_circ_225425 55809 RMVar_ID_55809 Human_SNP_ID_180778751 m1A Human chr4 - 39458415 39458415 39458415 GTTTCAGAATGAAGACTATTCTCAGCAATCAGACTGTCGACATTCCAGAAAATGGTATGAGACTT GTTTCAGAATGAAGACTATTCTCAGCAATCAGGCTGTCGACATTCCAGAAAATGGTATGAGACTT T C RPL9 Ensembl:ENSG00000163682 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs748978517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_620184,Human_RBP_ID_1638475,Human_RBP_ID_1978468,Human_RBP_ID_4795386,Human_RBP_ID_5150624,Human_RBP_ID_8591156,Human_RBP_ID_9334677,Human_RBP_ID_15146870,Human_RBP_ID_22826145 Human_Splice_Rec_554792,Human_Splice_Rec_554793,Human_Splice_Rec_554806,Human_Splice_Rec_554807,Human_Splice_Rec_554820,Human_Splice_Rec_554835,Human_Splice_Rec_554872,Human_Splice_Rec_554873,Human_Splice_Rec_554885,Human_Splice_Rec_554896,Human_Splice_Rec_554897,Human_Splice_Rec_554904,Human_Splice_Rec_554909,Human_Splice_Rec_554913,Human_Splice_Rec_554918,Human_Splice_Rec_554919,Human_Splice_Rec_554922 Human_miRNA_ID_1933077,Human_miRNA_ID_2196884,Human_miRNA_ID_2935889 RMVar_hsa_circ_121552,RMVar_hsa_circ_225436,RMVar_hsa_circ_84999,RMVar_hsa_circ_225435,RMVar_hsa_circ_82155,RMVar_hsa_circ_225441 55810 RMVar_ID_55810 Human_SNP_ID_180778903 m1A Human chr4 - 39458803 39458803 39458803 GGAAAGGCTGCGGCGCGGCTCCCACTCTCGGAACCTTGTCCTGTTTGTCCCCCAGCTCGGCAAGC GGAAAGGCTGCGGCGCGGCTCCCACTCTCGGAGCCTTGTCCTGTTTGTCCCCCAGCTCGGCAAGC T C RPL9 Ensembl:ENSG00000163682 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:39458789..39458897 26863196 MeRIP-seq:(Medium) rs1232725534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786206,Human_RBP_ID_837498,Human_RBP_ID_4784935,Human_RBP_ID_5394029,Human_RBP_ID_19121605,Human_RBP_ID_22481256,Human_RBP_ID_23258857,Human_RBP_ID_26791220 RMVar_hsa_circ_84999,RMVar_hsa_circ_225435 55811 RMVar_ID_55811 Human_SNP_ID_180778960 m1A Human chr4 - 39458892 39458892 39458892 ACAGACGTTCTTTCTTTGCTGCGTCTACTGCGAGGTAAGGATGTTTCTGTGCTCGTGGGGGTACT ACAGACGTTCTTTCTTTGCTGCGTCTACTGCGGGGTAAGGATGTTTCTGTGCTCGTGGGGGTACT T C RPL9 Ensembl:ENSG00000163682 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1446181927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249122,Human_RBP_ID_620198,Human_RBP_ID_786207,Human_RBP_ID_837499,Human_RBP_ID_4795389,Human_RBP_ID_5150625,Human_RBP_ID_5241947,Human_RBP_ID_5395271,Human_RBP_ID_5507994,Human_RBP_ID_9335000,Human_RBP_ID_17661680,Human_RBP_ID_18424888,Human_RBP_ID_19122430,Human_RBP_ID_22095486,Human_RBP_ID_22457674,Human_RBP_ID_22481256,Human_RBP_ID_23213758,Human_RBP_ID_24054609,Human_RBP_ID_24554238 Human_Splice_Rec_554791,Human_Splice_Rec_554805,Human_Splice_Rec_554819,Human_Splice_Rec_554847,Human_Splice_Rec_554871,Human_Splice_Rec_554883,Human_Splice_Rec_554895,Human_Splice_Rec_554903,Human_Splice_Rec_554917,Human_Splice_Rec_554921 RMVar_hsa_circ_84999,RMVar_hsa_circ_225435 55812 RMVar_ID_55812 Human_SNP_ID_180822103 m1A Human chr4 - 39638834 39638834 39638834 CGGCCAGAAACGGCAGTGGCAGCAGCGTCCGGAGCAGCCGCAGCCTTCTGGAAGCTCCAGGCGGT CGGCCAGAAACGGCAGTGGCAGCAGCGTCCGGTGCAGCCGCAGCCTTCTGGAAGCTCCAGGCGGT T A SMIM14 Ensembl:ENSG00000163683 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:39638725..39638985 26863196 MeRIP-seq:(Medium) rs893237437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795395 Human_Splice_Rec_555337,Human_Splice_Rec_555351,Human_Splice_Rec_555363,Human_Splice_Rec_555369 55813 RMVar_ID_55813 Human_SNP_ID_180837049 m1A Human chr4 + 39698255 39698238 39698256 GTCTGAATCGCCGAGGGAGGAGGCGGTGGAGGAAGAGGTGGCGGCGGTGGCGGTGGTCGTAGCGG GTCTGAATCGCCGAGG__________________GAGGTGGCGGCGGTGGCGGTGGTCGTAGCGG GGAGGAGGCGGTGGAGGAA G UBE2K Ensembl:ENSG00000078140 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:39698126..39737500;chr4:39698093..39755706 26863196 MeRIP-seq:(Medium) rs1199947195 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_620253,Human_RBP_ID_3747389,Human_RBP_ID_3966186,Human_RBP_ID_4794912,Human_RBP_ID_5475517,Human_RBP_ID_8211721,Human_RBP_ID_9160072,Human_RBP_ID_9354503,Human_RBP_ID_18424578,Human_RBP_ID_22457676,Human_RBP_ID_23034856,Human_RBP_ID_24547768,Human_RBP_ID_27841831 Human_Splice_Rec_555447 55814 RMVar_ID_55814 Human_SNP_ID_180837089 m1A Human chr4 + 39698401 39698401 39698401 GGAGGTGCTGAAGAGCGAGGAGGTCAGAAATGAACTCCCGGATATCCCCCACCTCTGCCTGGGGC GGAGGTGCTGAAGAGCGAGGAGGTCAGAAATGGACTCCCGGATATCCCCCACCTCTGCCTGGGGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:39698395..39698504 32194978 MeRIP-seq:(Medium) rs1382737406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19121612 55815 RMVar_ID_55815 Human_SNP_ID_180850449 m1A Human chr4 + 39745768 39745768 39745768 TTCCCCATTTTTTTAGGAGGAAGATACCAACTAGAGATAAAAATACCAGAAACATACCCATTTAA TTCCCCATTTTTTTAGGAGGAAGATACCAACTCGAGATAAAAATACCAGAAACATACCCATTTAA A C UBE2K Ensembl:ENSG00000078140 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:39745751..39745825 26863196 MeRIP-seq:(Medium) rs1301301774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_620263,Human_RBP_ID_942383,Human_RBP_ID_22609851,Human_RBP_ID_22679106 Human_Splice_Rec_555423,Human_Splice_Rec_555429,Human_Splice_Rec_555438,Human_Splice_Rec_555439,Human_Splice_Rec_555449,Human_Splice_Rec_555467 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225470,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_276276,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_292205,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225469,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 55816 RMVar_ID_55816 Human_SNP_ID_180881841 m1A Human chr4 + 39853670 39853670 39853670 CCACCCCATAAATTCTTCTTTTTGAAGACCTCACCTCAATTTATTACCATCGTTTCTTTTACCTA CCACCCCATAAATTCTTCTTTTTGAAGACCTCCCCTCAATTTATTACCATCGTTTCTTTTACCTA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:39853634..39853812 26863196 MeRIP-seq:(Medium) rs546077896 Functional Loss SNV dbSNP153 33..33 33 - - - 55817 RMVar_ID_55817 Human_SNP_ID_180914525 m1A Human chr4 - 39977499 39977497 39977499 CGACTAGGGGCGGCGGCGCAACCACCTGACAGAGGCCCGGGCGCTCGATGCACCTTCCGCCCGCA CGACTAGGGGCGGCGGCGCAACCACCTGACAG__GCCCGGGCGCTCGATGCACCTTCCGCCCGCA CCT C PDS5A Ensembl:ENSG00000121892 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:39977476..39977500 26863196 MeRIP-seq:(Medium) rs1325688941 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_248943,Human_RBP_ID_4794592,Human_RBP_ID_8881970,Human_RBP_ID_9304353,Human_RBP_ID_9397126,Human_RBP_ID_18424745,Human_RBP_ID_22095490 Human_Splice_Rec_555481,Human_Splice_Rec_555561,Human_Splice_Rec_555609 Human_miRNA_ID_2442823 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_225524 55818 RMVar_ID_55818 Human_SNP_ID_180914527 m1A Human chr4 - 39977508 39977508 39977508 TGTGCAGCCCGACTAGGGGCGGCGGCGCAACCACCTGACAGAGGCCCGGGCGCTCGATGCACCTT TGTGCAGCCCGACTAGGGGCGGCGGCGCAACCCCCTGACAGAGGCCCGGGCGCTCGATGCACCTT T G PDS5A Ensembl:ENSG00000121892 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:39977451..39977850 26863196 MeRIP-seq:(Medium) rs1396469188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794592,Human_RBP_ID_8881970,Human_RBP_ID_9304353,Human_RBP_ID_9397126,Human_RBP_ID_18424745,Human_RBP_ID_22095490 Human_Splice_Rec_555481,Human_Splice_Rec_555561,Human_Splice_Rec_555609 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_225524 55819 RMVar_ID_55819 Human_SNP_ID_180914580 m1A Human chr4 - 39977609 39977609 39977609 CCCCGCGGCGGCTGCTCCTCCTCGGCACCGCCAGCCCCAGCGCCGCTCCCGGGCGGGCGGGCGGC CCCCGCGGCGGCTGCTCCTCCTCGGCACCGCCGGCCCCAGCGCCGCTCCCGGGCGGGCGGGCGGC T C PDS5A Ensembl:ENSG00000121892 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:39977451..39977906 26863196 MeRIP-seq:(Medium) rs1417102347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794592,Human_RBP_ID_5242097,Human_RBP_ID_9304353,Human_RBP_ID_18195017,Human_RBP_ID_18424745,Human_RBP_ID_18471856 Human_miRNA_ID_2683497 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_225524 55820 RMVar_ID_55820 Human_SNP_ID_180914632 m1A Human chr4 - 39977744 39977744 39977744 GTGCGGGCGGGCCGCGGGGGTCCCGGACGGACACAAGCGCACACACTCCCGGAGGAGCCTTCGAG GTGCGGGCGGGCCGCGGGGGTCCCGGACGGACCCAAGCGCACACACTCCCGGAGGAGCCTTCGAG T G PDS5A Ensembl:ENSG00000121892 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:39977457..39977936 26863196 MeRIP-seq:(Medium) rs1222189776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794593,Human_RBP_ID_8881971,Human_RBP_ID_9304354,Human_RBP_ID_17154609 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_225524 55821 RMVar_ID_55821 Human_SNP_ID_180962932 m1A Human chr4 + 40164138 40164135 40164139 ACGATGCTGTATGTGTAAGGTTGAAAAGCTTGACTGTGAGATACAGGCTGGTAAGGAGTCAAGTG ACGATGCTGTATGTGTAAGGTTGAAAAGCT____TGTGAGATACAGGCTGGTAAGGAGTCAAGTG TTGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:40164088..40164203 26863196 MeRIP-seq:(Medium) rs1481873369 Functional Loss DEL dbSNP153 31..34 33 - - - 55822 RMVar_ID_55822 Human_SNP_ID_181050543 m1A Human chr4 + 40516056 40516056 40516056 CGGGGCGTGGCAACAGGGCCTCCCCGCCCCCCAGCCCTGCCTGTCAGCTCCTTTTGCTTTCACAA CGGGGCGTGGCAACAGGGCCTCCCCGCCCCCCCGCCCTGCCTGTCAGCTCCTTTTGCTTTCACAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:40516045..40516129 26863196 MeRIP-seq:(Medium) rs1204428911 Functional Loss SNV dbSNP153 33..33 33 - - - 55823 RMVar_ID_55823 Human_SNP_ID_181203582 m1A Human chr4 + 41128918 41128918 41128918 CTGATTGGCATTTCCAGCCCCTTGCATCCTTTACCTGCCTTTCCTACTACAGACAACACTGTCAA CTGATTGGCATTTCCAGCCCCTTGCATCCTTTGCCTGCCTTTCCTACTACAGACAACACTGTCAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41128917..41129079 26863196 MeRIP-seq:(Medium) rs1447284456 Functional Loss SNV dbSNP153 33..33 33 - - - 55824 RMVar_ID_55824 Human_SNP_ID_181206784 m1A Human chr4 + 41143112 41143112 41143112 GGCAGATCCGACCACAGCATGCTTGGCTACAGACCACAGCAGCTCACCCACAGCAACTCCAACCT GGCAGATCCGACCACAGCATGCTTGGCTACAGCCCACAGCAGCTCACCCACAGCAACTCCAACCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41143063..41143183 26863196 MeRIP-seq:(Medium) rs1460753085 Functional Loss SNV dbSNP153 33..33 33 - - - 55825 RMVar_ID_55825 Human_SNP_ID_181223573 m1A Human chr4 - 41214454 41214454 41214454 TGATCTGGGCGCTCCGGGAAGGGCGAGACTGGAGCAGAGCCGCTGGGCGCCGGAGCCGAGGCGAG TGATCTGGGCGCTCCGGGAAGGGCGAGACTGGGGCAGAGCCGCTGGGCGCCGGAGCCGAGGCGAG T C APBB2 Ensembl:ENSG00000163697 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41214396..41214485 26863196 MeRIP-seq:(Medium) rs1298122118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5475919,Human_RBP_ID_18424579,Human_RBP_ID_23034857,Human_RBP_ID_23120131 Human_Splice_Rec_556043,Human_Splice_Rec_556075,Human_Splice_Rec_556117,Human_Splice_Rec_556183,Human_Splice_Rec_556327,Human_Splice_Rec_556335,Human_Splice_Rec_556343,Human_Splice_Rec_556349,Human_Splice_Rec_556357,Human_Splice_Rec_556367,Human_Splice_Rec_556383,Human_Splice_Rec_556397 55826 RMVar_ID_55826 Human_SNP_ID_181223577 m1A Human chr4 - 41214459 41214459 41214459 GCATCTGATCTGGGCGCTCCGGGAAGGGCGAGACTGGAGCAGAGCCGCTGGGCGCCGGAGCCGAG GCATCTGATCTGGGCGCTCCGGGAAGGGCGAGTCTGGAGCAGAGCCGCTGGGCGCCGGAGCCGAG T A APBB2 Ensembl:ENSG00000163697 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41214365..41214500 26863196 MeRIP-seq:(Medium) rs993614301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5475919,Human_RBP_ID_18424579,Human_RBP_ID_23034857,Human_RBP_ID_23120131 Human_Splice_Rec_556043,Human_Splice_Rec_556075,Human_Splice_Rec_556117,Human_Splice_Rec_556183,Human_Splice_Rec_556327,Human_Splice_Rec_556335,Human_Splice_Rec_556343,Human_Splice_Rec_556349,Human_Splice_Rec_556357,Human_Splice_Rec_556367,Human_Splice_Rec_556383,Human_Splice_Rec_556397 55827 RMVar_ID_55827 Human_SNP_ID_181223594 m1A Human chr4 - 41214484 41214484 41214484 AGTAGGAAGCTAGTGCGCTGTAACCGCATCTGATCTGGGCGCTCCGGGAAGGGCGAGACTGGAGC AGTAGGAAGCTAGTGCGCTGTAACCGCATCTGTTCTGGGCGCTCCGGGAAGGGCGAGACTGGAGC T A APBB2 Ensembl:ENSG00000163697 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41214393..41214509 26863196 MeRIP-seq:(Medium) rs1179540038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4799532,Human_RBP_ID_5475919,Human_RBP_ID_18424579,Human_RBP_ID_23034857,Human_RBP_ID_23120131 Human_Splice_Rec_556043,Human_Splice_Rec_556075,Human_Splice_Rec_556117,Human_Splice_Rec_556183,Human_Splice_Rec_556327,Human_Splice_Rec_556335,Human_Splice_Rec_556343,Human_Splice_Rec_556349,Human_Splice_Rec_556357,Human_Splice_Rec_556367,Human_Splice_Rec_556383,Human_Splice_Rec_556397 55828 RMVar_ID_55828 Human_SNP_ID_181258653 m1A Human chr4 - 41359474 41359474 41359474 GTGTCTGTAAGGAAATGTCCTGAAGAGGTGACATGAGTGAGGGAGATTTAACTGTGTAACAATTT GTGTCTGTAAGGAAATGTCCTGAAGAGGTGACGTGAGTGAGGGAGATTTAACTGTGTAACAATTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41359275..41359506 26863196 MeRIP-seq:(Medium) rs1561110922 Functional Loss SNV dbSNP153 33..33 33 - - - 55829 RMVar_ID_55829 Human_SNP_ID_181259018 m1A Human chr4 + 41360631 41360631 41360631 GGCGCCTCCGCGCTCGCTCCCGCGGGTCACTCACGGCGCGTTGGAGCCCGGGCGGCGCCGGGAAC GGCGCCTCCGCGCTCGCTCCCGCGGGTCACTCGCGGCGCGTTGGAGCCCGGGCGGCGCCGGGAAC A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41360489..41360722 26863196 MeRIP-seq:(Medium) rs1479887855 Functional Loss SNV dbSNP153 33..33 33 - - - 55830 RMVar_ID_55830 Human_SNP_ID_181259142 m1A Human chr4 - 41360911 41360911 41360911 CACCTACCTCAATCCACTTCTGCGCCTCGGAGAAGGCGGGCTCGGGGGGCGGCTCGGGCTGCAGG CACCTACCTCAATCCACTTCTGCGCCTCGGAGGAGGCGGGCTCGGGGGGCGGCTCGGGCTGCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41360623..41360973 26863196 MeRIP-seq:(Medium) rs1243164276 Functional Loss SNV dbSNP153 33..33 33 - - - 55831 RMVar_ID_55831 Human_SNP_ID_181259150 m1A Human chr4 + 41360931 41360927 41360932 CCGAGCCCGCCTTCTCCGAGGCGCAGAAGTGGATTGAGGTAGGTGCGGGTGGCTGGCGGGCGGCC CCGAGCCCGCCTTCTCCGAGGCGCAGAAG_____TGAGGTAGGTGCGGGTGGCTGGCGGGCGGCC GTGGAT G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:41360825..41361029 26863196 MeRIP-seq:(Medium) rs1037285057 Functional Loss DEL dbSNP153 30..34 33 - - - Human_Splice_Rec_556611,Human_Splice_Rec_556623,Human_Splice_Rec_556673,Human_Splice_Rec_556723,Human_Splice_Rec_556775,Human_Splice_Rec_556781,Human_Splice_Rec_556825,Human_Splice_Rec_556835 55832 RMVar_ID_55832 Human_SNP_ID_181259150 m1A Human chr4 - 41360932 41360927 41360932 AGGCCGCCCGCCAGCCACCCGCACCTACCTCAATCCACTTCTGCGCCTCGGAGAAGGCGGGCTCG AGGCCGCCCGCCAGCCACCCGCACCTACCTCA_____CTTCTGCGCCTCGGAGAAGGCGGGCTCG GTGGAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41360775..41360994 26863196 MeRIP-seq:(Medium) rs1037285057 Functional Loss DEL dbSNP153 33..37 33 - - - 55833 RMVar_ID_55833 Human_SNP_ID_181263981 m1A Human chr4 + 41382469 41382469 41382469 GCCAAGGAAACAGGGCTATGAGTTTGTACTGTAGGCAGCAGTAGGGAGGGGGAATTGGAAGCAGG GCCAAGGAAACAGGGCTATGAGTTTGTACTGTGGGCAGCAGTAGGGAGGGGGAATTGGAAGCAGG A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41382463..41382560 26863196 MeRIP-seq:(Medium) rs548995373 Functional Loss SNV dbSNP153 33..33 33 - - - 55834 RMVar_ID_55834 Human_SNP_ID_181266882 m1A Human chr4 + 41395872 41395872 41395872 AAAGAGGCAAGAATGTATGTCAGACAGTGATAAGTGTCATGGAGAAAAATAAAGTAGGGCAGTGG AAAGAGGCAAGAATGTATGTCAGACAGTGATAGGTGTCATGGAGAAAAATAAAGTAGGGCAGTGG A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41395865..41396120 26863196 MeRIP-seq:(Medium) rs1310418944 Functional Loss SNV dbSNP153 33..33 33 - - - 55835 RMVar_ID_55835 Human_SNP_ID_181273674 m1A Human chr4 + 41423798 41423798 41423798 TTGAGAAGTTAAATTTTCGGTGAAAGTGCTATAAAGGTGTGGAGTTTGGGGGAAAGTAAGTGTTT TTGAGAAGTTAAATTTTCGGTGAAAGTGCTATCAAGGTGTGGAGTTTGGGGGAAAGTAAGTGTTT A C LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41423795..41423861 26863196 MeRIP-seq:(Medium) rs951063535 Functional Loss SNV dbSNP153 33..33 33 - - - 55836 RMVar_ID_55836 Human_SNP_ID_181287191 m1A Human chr4 - 41482569 41482569 41482569 TATTCTAATATTGTCATACTGTCTAACCCAAAAGACATTTTTCTCATTTGATTGTAACATCGCAG TATTCTAATATTGTCATACTGTCTAACCCAAAGGACATTTTTCTCATTTGATTGTAACATCGCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41482564..41482650 26863196 MeRIP-seq:(Medium) rs1028058107 Functional Loss SNV dbSNP153 33..33 33 - - - 55837 RMVar_ID_55837 Human_SNP_ID_181287192 m1A Human chr4 - 41482569 41482569 41482569 TATTCTAATATTGTCATACTGTCTAACCCAAAAGACATTTTTCTCATTTGATTGTAACATCGCAG TATTCTAATATTGTCATACTGTCTAACCCAAACGACATTTTTCTCATTTGATTGTAACATCGCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41482564..41482650 26863196 MeRIP-seq:(Medium) rs1028058107 Functional Loss SNV dbSNP153 33..33 33 - - - 55838 RMVar_ID_55838 Human_SNP_ID_181287279 m1A Human chr4 + 41482985 41482985 41482985 GATGGCTGAGCTATGATGATAGGGTAATGGGTATAGGATACTCATATAGGAAGTTTGGGCTGTGA GATGGCTGAGCTATGATGATAGGGTAATGGGTGTAGGATACTCATATAGGAAGTTTGGGCTGTGA A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41482982..41483216 26863196 MeRIP-seq:(Medium) rs1366690875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225663,RMVar_hsa_circ_304463,RMVar_hsa_circ_225662,RMVar_hsa_circ_225664 55839 RMVar_ID_55839 Human_SNP_ID_181307302 m1A Human chr4 + 41570749 41570749 41570749 GGTTAAAGACAGAAGGATGAATGGCACCGCCCAACAAAAATAGACTGATGAGAGTTATTGGCCAT GGTTAAAGACAGAAGGATGAATGGCACCGCCCGACAAAAATAGACTGATGAGAGTTATTGGCCAT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41570744..41570892 26863196 MeRIP-seq:(Medium) rs754893818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346246,RMVar_hsa_circ_362281,RMVar_hsa_circ_286989,RMVar_hsa_circ_69628 55840 RMVar_ID_55840 Human_SNP_ID_181307410 m1A Human chr4 + 41571193 41571193 41571193 GGAGCCACACAGTCCTTGGAGGACTGTTCGTTAGGGTAGAAATGTTTTTTGTCTTGTTTATAGGA GGAGCCACACAGTCCTTGGAGGACTGTTCGTTCGGGTAGAAATGTTTTTTGTCTTGTTTATAGGA A C LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:41571189..41571561 26863196 MeRIP-seq:(Medium) rs1428315985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346246,RMVar_hsa_circ_362281,RMVar_hsa_circ_286989,RMVar_hsa_circ_69628 55841 RMVar_ID_55841 Human_SNP_ID_181318260 m1A Human chr4 + 41619328 41619328 41619328 TGCCTTTTAACCAGTACCTCCCGAACAAAAGCAATCAGACGGCCTACGTCCCCGCGCCTCTGAGA TGCCTTTTAACCAGTACCTCCCGAACAAAAGCGATCAGACGGCCTACGTCCCCGCGCCTCTGAGA A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41619277..41619476 26863196 MeRIP-seq:(Medium) rs199548284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72422 RMVar_hsa_circ_346246,RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_1734,RMVar_hsa_circ_331102,RMVar_hsa_circ_64263,RMVar_hsa_circ_32676,RMVar_hsa_circ_225669,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_26880 55842 RMVar_ID_55842 Human_SNP_ID_181318261 m1A Human chr4 + 41619328 41619328 41619328 TGCCTTTTAACCAGTACCTCCCGAACAAAAGCAATCAGACGGCCTACGTCCCCGCGCCTCTGAGA TGCCTTTTAACCAGTACCTCCCGAACAAAAGCTATCAGACGGCCTACGTCCCCGCGCCTCTGAGA A T LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41619277..41619476 26863196 MeRIP-seq:(Medium) rs199548284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72422 RMVar_hsa_circ_346246,RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_1734,RMVar_hsa_circ_331102,RMVar_hsa_circ_64263,RMVar_hsa_circ_32676,RMVar_hsa_circ_225669,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_26880 55843 RMVar_ID_55843 Human_SNP_ID_181324472 m1A Human chr4 + 41644588 41644588 41644588 GCAGGGCCCGCCAGGAGCAGCTGCAGCTGATAAATAACCAGCTGAGGGAAGAGGACGACAAATGG GCAGGGCCCGCCAGGAGCAGCTGCAGCTGATACATAACCAGCTGAGGGAAGAGGACGACAAATGG A C LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41644538..41644791 26863196 MeRIP-seq:(Medium) rs1440294342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70678,Human_RBP_ID_2848327,Human_RBP_ID_5607423 Human_Splice_Rec_556576,Human_Splice_Rec_556577,Human_Splice_Rec_556640,Human_Splice_Rec_556641,Human_Splice_Rec_556690,Human_Splice_Rec_556691,Human_Splice_Rec_556740,Human_Splice_Rec_556741,Human_Splice_Rec_556798,Human_Splice_Rec_556799,Human_Splice_Rec_556850,Human_Splice_Rec_556851,Human_Splice_Rec_556950,Human_Splice_Rec_556951,Human_Splice_Rec_556996,Human_Splice_Rec_556997,Human_Splice_Rec_557034,Human_Splice_Rec_557035,Human_Splice_Rec_557072,Human_Splice_Rec_557073,Human_Splice_Rec_557118,Human_Splice_Rec_557119,Human_Splice_Rec_557156,Human_Splice_Rec_557157,Human_Splice_Rec_557194,Human_Splice_Rec_557195 RMVar_hsa_circ_4742,RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_64263,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_58538,RMVar_hsa_circ_50268,RMVar_hsa_circ_26880,RMVar_hsa_circ_111746,RMVar_hsa_circ_225671,RMVar_hsa_circ_10991,RMVar_hsa_circ_345000,RMVar_hsa_circ_345937,RMVar_hsa_circ_300387,RMVar_hsa_circ_225672,RMVar_hsa_circ_225673,RMVar_hsa_circ_225674 55844 RMVar_ID_55844 Human_SNP_ID_181324473 m1A Human chr4 + 41644588 41644588 41644588 GCAGGGCCCGCCAGGAGCAGCTGCAGCTGATAAATAACCAGCTGAGGGAAGAGGACGACAAATGG GCAGGGCCCGCCAGGAGCAGCTGCAGCTGATATATAACCAGCTGAGGGAAGAGGACGACAAATGG A T LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:41644538..41644791 26863196 MeRIP-seq:(Medium) rs1440294342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70678,Human_RBP_ID_2848327,Human_RBP_ID_5607423 Human_Splice_Rec_556576,Human_Splice_Rec_556577,Human_Splice_Rec_556640,Human_Splice_Rec_556641,Human_Splice_Rec_556690,Human_Splice_Rec_556691,Human_Splice_Rec_556740,Human_Splice_Rec_556741,Human_Splice_Rec_556798,Human_Splice_Rec_556799,Human_Splice_Rec_556850,Human_Splice_Rec_556851,Human_Splice_Rec_556950,Human_Splice_Rec_556951,Human_Splice_Rec_556996,Human_Splice_Rec_556997,Human_Splice_Rec_557034,Human_Splice_Rec_557035,Human_Splice_Rec_557072,Human_Splice_Rec_557073,Human_Splice_Rec_557118,Human_Splice_Rec_557119,Human_Splice_Rec_557156,Human_Splice_Rec_557157,Human_Splice_Rec_557194,Human_Splice_Rec_557195 RMVar_hsa_circ_4742,RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_64263,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_58538,RMVar_hsa_circ_50268,RMVar_hsa_circ_26880,RMVar_hsa_circ_111746,RMVar_hsa_circ_225671,RMVar_hsa_circ_10991,RMVar_hsa_circ_345000,RMVar_hsa_circ_345937,RMVar_hsa_circ_300387,RMVar_hsa_circ_225672,RMVar_hsa_circ_225673,RMVar_hsa_circ_225674 55845 RMVar_ID_55845 Human_SNP_ID_181324817 m1A Human chr4 + 41646228 41646228 41646228 AAATGGAGAAGTTACTGGCTGGAGAAGATGGGACAAGTGAACGAAGGAAAAGCATCAAAACCTAC AAATGGAGAAGTTACTGGCTGGAGAAGATGGGGCAAGTGAACGAAGGAAAAGCATCAAAACCTAC A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41646101..41646300 26863196 MeRIP-seq:(Medium) rs759377652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2848332,Human_RBP_ID_27508408 Human_Splice_Rec_556579,Human_Splice_Rec_556643,Human_Splice_Rec_556693,Human_Splice_Rec_556743,Human_Splice_Rec_556801,Human_Splice_Rec_556853,Human_Splice_Rec_556953,Human_Splice_Rec_556999,Human_Splice_Rec_557037,Human_Splice_Rec_557075,Human_Splice_Rec_557121,Human_Splice_Rec_557159,Human_Splice_Rec_557197 RMVar_hsa_circ_4742,RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_64263,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_58538,RMVar_hsa_circ_50268,RMVar_hsa_circ_26880,RMVar_hsa_circ_111746,RMVar_hsa_circ_225671,RMVar_hsa_circ_10991,RMVar_hsa_circ_345000,RMVar_hsa_circ_345937,RMVar_hsa_circ_300387,RMVar_hsa_circ_225672,RMVar_hsa_circ_225673,RMVar_hsa_circ_225674 55846 RMVar_ID_55846 Human_SNP_ID_181327153 m1A Human chr4 - 41655834 41655834 41655834 GAGGGAACAAAAGGAGAGGCAAAAAGAGCTGCAGGAAGGGCCAGGCATGGTGGCTCATGCCTATA GAGGGAACAAAAGGAGAGGCAAAAAGAGCTGCCGGAAGGGCCAGGCATGGTGGCTCATGCCTATA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:41655824..41655956 26863196 MeRIP-seq:(Medium) rs78977830 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6639,GWAS_ID_6640,GWAS_ID_6641,GWAS_ID_6642,GWAS_ID_6643,GWAS_ID_6644,GWAS_ID_6645,GWAS_ID_6646,GWAS_ID_6647,GWAS_ID_6648,GWAS_ID_6649,GWAS_ID_6650,GWAS_ID_6651,GWAS_ID_6652,GWAS_ID_6653,GWAS_ID_6654,GWAS_ID_6655,GWAS_ID_6656,GWAS_ID_6657 55847 RMVar_ID_55847 Human_SNP_ID_181331735 m1A Human chr4 + 41676461 41676461 41676461 AAAATGGCAACAGGAACAGGAACGTTTGCTCCAGGTAGGATGGAGTTTGCTGCTTTTTTTGTTTT AAAATGGCAACAGGAACAGGAACGTTTGCTCCGGGTAGGATGGAGTTTGCTGCTTTTTTTGTTTT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41676420..41676511 26863196 MeRIP-seq:(Medium) rs763336859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_556594,Human_Splice_Rec_556595,Human_Splice_Rec_556656,Human_Splice_Rec_556657,Human_Splice_Rec_556706,Human_Splice_Rec_556707,Human_Splice_Rec_556756,Human_Splice_Rec_556757,Human_Splice_Rec_556868,Human_Splice_Rec_556869,Human_Splice_Rec_556966,Human_Splice_Rec_556967,Human_Splice_Rec_557012,Human_Splice_Rec_557013,Human_Splice_Rec_557050,Human_Splice_Rec_557051,Human_Splice_Rec_557088,Human_Splice_Rec_557089,Human_Splice_Rec_557134,Human_Splice_Rec_557135,Human_Splice_Rec_557172,Human_Splice_Rec_557173,Human_Splice_Rec_557210,Human_Splice_Rec_557211 RMVar_hsa_circ_4742,RMVar_hsa_circ_69628,RMVar_hsa_circ_225676,RMVar_hsa_circ_55165,RMVar_hsa_circ_360337,RMVar_hsa_circ_338796,RMVar_hsa_circ_290484,RMVar_hsa_circ_65694,RMVar_hsa_circ_225677,RMVar_hsa_circ_265953,RMVar_hsa_circ_293855,RMVar_hsa_circ_277058,RMVar_hsa_circ_6109,RMVar_hsa_circ_31233,RMVar_hsa_circ_225683,RMVar_hsa_circ_225684,RMVar_hsa_circ_41883 55848 RMVar_ID_55848 Human_SNP_ID_181332561 m1A Human chr4 + 41680080 41680080 41680080 GAAAAGGCCCAAAAGGAGGTGGAAGAGGAAGAACGCAGATACTATGAGGAGGTAGGAAATTCCCA GAAAAGGCCCAAAAGGAGGTGGAAGAGGAAGAGCGCAGATACTATGAGGAGGTAGGAAATTCCCA A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41679963..41680139 26863196 MeRIP-seq:(Medium) rs750562823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607434 Human_Splice_Rec_556596,Human_Splice_Rec_556597,Human_Splice_Rec_556658,Human_Splice_Rec_556659,Human_Splice_Rec_556708,Human_Splice_Rec_556709,Human_Splice_Rec_556758,Human_Splice_Rec_556759,Human_Splice_Rec_556810,Human_Splice_Rec_556811,Human_Splice_Rec_556870,Human_Splice_Rec_556871,Human_Splice_Rec_556968,Human_Splice_Rec_556969,Human_Splice_Rec_557014,Human_Splice_Rec_557015,Human_Splice_Rec_557052,Human_Splice_Rec_557053,Human_Splice_Rec_557090,Human_Splice_Rec_557091,Human_Splice_Rec_557136,Human_Splice_Rec_557137,Human_Splice_Rec_557174,Human_Splice_Rec_557175,Human_Splice_Rec_557212,Human_Splice_Rec_557213 RMVar_hsa_circ_4742,RMVar_hsa_circ_69628,RMVar_hsa_circ_225676,RMVar_hsa_circ_55165,RMVar_hsa_circ_360337,RMVar_hsa_circ_338796,RMVar_hsa_circ_65694,RMVar_hsa_circ_9240,RMVar_hsa_circ_265953,RMVar_hsa_circ_293855,RMVar_hsa_circ_6109,RMVar_hsa_circ_31233,RMVar_hsa_circ_52401,RMVar_hsa_circ_225684,RMVar_hsa_circ_41883,RMVar_hsa_circ_336352,RMVar_hsa_circ_18750,RMVar_hsa_circ_225685,RMVar_hsa_circ_225686 55849 RMVar_ID_55849 Human_SNP_ID_181332741 m1A Human chr4 + 41680905 41680905 41680905 AAAGTGCCTTAATGACATTTTTGTCTTGACAAATATGATTTTTATTTTCCCCCCTTTCATCGATT AAAGTGCCTTAATGACATTTTTGTCTTGACAAGTATGATTTTTATTTTCCCCCCTTTCATCGATT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41680902..41680975 26863196 MeRIP-seq:(Medium) rs371805492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4742,RMVar_hsa_circ_69628,RMVar_hsa_circ_225676,RMVar_hsa_circ_55165,RMVar_hsa_circ_360337,RMVar_hsa_circ_338796,RMVar_hsa_circ_65694,RMVar_hsa_circ_9240,RMVar_hsa_circ_265953,RMVar_hsa_circ_293855,RMVar_hsa_circ_31233,RMVar_hsa_circ_52401,RMVar_hsa_circ_41883,RMVar_hsa_circ_336352,RMVar_hsa_circ_18750,RMVar_hsa_circ_225685,RMVar_hsa_circ_225686 55850 RMVar_ID_55850 Human_SNP_ID_181336615 m1A Human chr4 + 41698285 41698285 41698285 TCTGTGATCAGCAAGAACCTACAGCACAGATTATGCCCTGCCCACTTCAATGAATACCTACTCTC TCTGTGATCAGCAAGAACCTACAGCACAGATTGTGCCCTGCCCACTTCAATGAATACCTACTCTC A G LIMCH1 Ensembl:ENSG00000064042 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41698237..41698335 26863196 MeRIP-seq:(Medium) rs116807154 Functional Loss SNV dbSNP153 33..33 33 - - - 55851 RMVar_ID_55851 Human_SNP_ID_181394594 m1A Human chr4 + 41935389 41935389 41935389 GCATCCGGCCTGTGTGTGGCGCGAGGCAGGGAAGCCGGTACCCGGGTCCTGGCCCCAGCGCTGAC GCATCCGGCCTGTGTGTGGCGCGAGGCAGGGAGGCCGGTACCCGGGTCCTGGCCCCAGCGCTGAC A G TMEM33 Ensembl:ENSG00000109133 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:41935151..41935550 26863196 MeRIP-seq:(Medium) rs368971723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248863,Human_RBP_ID_838131,Human_RBP_ID_939964,Human_RBP_ID_4785666,Human_RBP_ID_8943682,Human_RBP_ID_22457865,Human_RBP_ID_22680169 RMVar_hsa_circ_77638,RMVar_hsa_circ_225689 55852 RMVar_ID_55852 Human_SNP_ID_181394604 m1A Human chr4 + 41935413 41935413 41935413 GGCAGGGAAGCCGGTACCCGGGTCCTGGCCCCAGCGCTGACGTTTTCTCTCCCCTTTCTTCTCTC GGCAGGGAAGCCGGTACCCGGGTCCTGGCCCCGGCGCTGACGTTTTCTCTCCCCTTTCTTCTCTC A G TMEM33 Ensembl:ENSG00000109133 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:41935326..41935500 26863410 MeRIP-seq:(Medium) rs1360966171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_620705,Human_RBP_ID_4794597,Human_RBP_ID_5448730,Human_RBP_ID_5475533,Human_RBP_ID_5508023,Human_RBP_ID_7311132,Human_RBP_ID_22457865,Human_RBP_ID_22680169,Human_RBP_ID_23289459,Human_RBP_ID_24055651 Human_miRNA_ID_2135924,Human_miRNA_ID_2683500 RMVar_hsa_circ_77638,RMVar_hsa_circ_225689 55853 RMVar_ID_55853 Human_SNP_ID_181394605 m1A Human chr4 + 41935413 41935413 41935413 GGCAGGGAAGCCGGTACCCGGGTCCTGGCCCCAGCGCTGACGTTTTCTCTCCCCTTTCTTCTCTC GGCAGGGAAGCCGGTACCCGGGTCCTGGCCCCTGCGCTGACGTTTTCTCTCCCCTTTCTTCTCTC A T TMEM33 Ensembl:ENSG00000109133 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:41935326..41935500 26863410 MeRIP-seq:(Medium) rs1360966171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_620705,Human_RBP_ID_4794597,Human_RBP_ID_5448730,Human_RBP_ID_5475533,Human_RBP_ID_5508023,Human_RBP_ID_7311132,Human_RBP_ID_22457865,Human_RBP_ID_22680169,Human_RBP_ID_23289459,Human_RBP_ID_24055651 Human_miRNA_ID_2135924,Human_miRNA_ID_2683500 RMVar_hsa_circ_77638,RMVar_hsa_circ_225689 55854 RMVar_ID_55854 Human_SNP_ID_181394617 m1A Human chr4 - 41935446 41935443 41935447 TCACACTAGCGTCTGCGACGCCGCAACCGCGAAGAGAGAAGAAAGGGGAGAGAAAACGTCAGCGC TCACACTAGCGTCTGCGACGCCGCAACCGCG____GAGAAGAAAGGGGAGAGAAAACGTCAGCGC CTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:41935396..41935480 26863196 MeRIP-seq:(Medium) rs1306037439 Functional Loss DEL dbSNP153 32..35 33 - - - 55855 RMVar_ID_55855 Human_SNP_ID_181394635 m1A Human chr4 + 41935478 41935478 41935478 TTCGCGGTTGCGGCGTCGCAGACGCTAGTGTGAGCCCCCATGGCAGATACGACCCCGAACGGCCC TTCGCGGTTGCGGCGTCGCAGACGCTAGTGTGGGCCCCCATGGCAGATACGACCCCGAACGGCCC A G TMEM33 Ensembl:ENSG00000109133 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:41935151..41938641 26863196 MeRIP-seq:(Medium) rs1173136084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70874,Human_RBP_ID_4795409,Human_RBP_ID_9334682,Human_RBP_ID_15155654,Human_RBP_ID_18026376,Human_RBP_ID_22457677,Human_RBP_ID_24055652,Human_RBP_ID_24430634,Human_RBP_ID_27327252 Human_Splice_Rec_557285,Human_Splice_Rec_557298,Human_Splice_Rec_557299,Human_Splice_Rec_557311,Human_Splice_Rec_557321,Human_Splice_Rec_557333,Human_Splice_Rec_557337,Human_Splice_Rec_557349 Human_miRNA_ID_2449814 RMVar_hsa_circ_9786,RMVar_hsa_circ_77638,RMVar_hsa_circ_225689 55856 RMVar_ID_55856 Human_SNP_ID_181413687 m1A Human chr4 + 42014814 42014814 42014814 GTTAAGTGAAATAAGGCAGGCACAGAAAGAAAAACAGCACGTTCTCACTTATTTATGGAGCTAAA GTTAAGTGAAATAAGGCAGGCACAGAAAGAAAGACAGCACGTTCTCACTTATTTATGGAGCTAAA A G SLC30A9 Ensembl:ENSG00000014824 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:42014810..42014969 26863196 MeRIP-seq:(Medium) rs925901058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225697,RMVar_hsa_circ_282527,RMVar_hsa_circ_357506,RMVar_hsa_circ_374894,RMVar_hsa_circ_378198,RMVar_hsa_circ_370102,RMVar_hsa_circ_318488,RMVar_hsa_circ_312608,RMVar_hsa_circ_114044,RMVar_hsa_circ_278359,RMVar_hsa_circ_280725,RMVar_hsa_circ_267452,RMVar_hsa_circ_225699,RMVar_hsa_circ_225701,RMVar_hsa_circ_225700,RMVar_hsa_circ_225698,RMVar_hsa_circ_225693,RMVar_hsa_circ_225695,RMVar_hsa_circ_225696,RMVar_hsa_circ_225694 55857 RMVar_ID_55857 Human_SNP_ID_181511834 m1A Human chr4 + 42401159 42401159 42401159 GCAGCCAATCCGCTTCTCACTCCGCAGCTATCAGACAGAGACCCTGCCCATGATCCTGACCTCCA GCAGCCAATCCGCTTCTCACTCCGCAGCTATCGGACAGAGACCCTGCCCATGATCCTGACCTCCA A G SHISA3 Ensembl:ENSG00000178343 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:42401064..42401226 26863196 MeRIP-seq:(Medium) rs759813601 Functional Loss SNV dbSNP153 33..33 33 - - - 55858 RMVar_ID_55858 Human_SNP_ID_218572718 m1A Human chr5 + 83126 83126 83126 GATGCTAAACATGAAACTATAAACTGGGTATCAGCATAAGTGATTCACAGGGTATGTTACTGGGA GATGCTAAACATGAAACTATAAACTGGGTATCGGCATAAGTGATTCACAGGGTATGTTACTGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:83123..83239 26863196 MeRIP-seq:(Medium) rs1415969701 Functional Loss SNV dbSNP153 33..33 33 - - - 55859 RMVar_ID_55859 Human_SNP_ID_218572960 m1A Human chr5 + 83376 83362 83376 CGATGAGAGGCCGGGTGGTCGGGGAAGGCTCGATGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG CGATGAGAGGCCGGGTGGT______________TGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG TCGGGGAAGGCTCGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:83321..83465;chr5:83313..83481 26863196 MeRIP-seq:(Medium) rs1479515641 Functional Loss DEL dbSNP153 20..33 33 - - - 55860 RMVar_ID_55860 Human_SNP_ID_218572973 m1A Human chr5 + 83376 83376 83376 CGATGAGAGGCCGGGTGGTCGGGGAAGGCTCGATGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG CGATGAGAGGCCGGGTGGTCGGGGAAGGCTCGCTGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:83321..83465;chr5:83313..83481 26863196 MeRIP-seq:(Medium) rs1196694148 Functional Loss SNV dbSNP153 33..33 33 - - - 55861 RMVar_ID_55861 Human_SNP_ID_218572974 m1A Human chr5 + 83376 83376 83376 CGATGAGAGGCCGGGTGGTCGGGGAAGGCTCGATGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG CGATGAGAGGCCGGGTGGTCGGGGAAGGCTCGGTGAGAGGCAGGGTGGTCGGGGAAGCTTCGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:83321..83465;chr5:83313..83481 26863196 MeRIP-seq:(Medium) rs1196694148 Functional Loss SNV dbSNP153 33..33 33 - - - 55862 RMVar_ID_55862 Human_SNP_ID_218573914 m1A Human chr5 + 85464 85284 85464 TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA _________________________________GGGAAGCCTCGATGAGAGGCAGCGAGCAGACA GGGGAAGCCTCGATGAGAGGCCGGGTGGTCGGGGAAGCCTTGATGAGAGGCCGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCGGGGAAGCCTCGATGGGAGGCAGGGTGGTCGGGGAAGCCTCGATGGGAGGCAGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:85406..85566 26863196 MeRIP-seq:(Medium) rs1560883340 Functional Loss DEL dbSNP153 1..33 33 - - - 55863 RMVar_ID_55863 Human_SNP_ID_218573995 m1A Human chr5 + 85464 85374 85464 TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA _________________________________GGGAAGCCTCGATGAGAGGCAGCGAGCAGACA GGGGAAGCCTCGATGGGAGGCAGGGTGGTCGGGGAAGCCTCGATGGGAGGCAGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:85406..85566 26863196 MeRIP-seq:(Medium) rs1560883427 Functional Loss DEL dbSNP153 1..33 33 - - - 55864 RMVar_ID_55864 Human_SNP_ID_218574012 m1A Human chr5 + 85479 85389 85479 TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACATACGCAGGAGGGAGG _________________________________GAGGCAGCGAGCAGACATACGCAGGAGGGAGG GGAGGCAGGGTGGTCGGGGAAGCCTCGATGGGAGGCAGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:85477..85568 26863196 MeRIP-seq:(Medium) rs1560883450 Functional Loss DEL dbSNP153 1..33 33 - - - 55865 RMVar_ID_55865 Human_SNP_ID_218574029 m1A Human chr5 + 85464 85404 85464 TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA _________________________________GGGAAGCCTCGATGAGAGGCAGCGAGCAGACA GGGGAAGCCTCGATGGGAGGCAGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:85406..85566 26863196 MeRIP-seq:(Medium) rs1560883469 Functional Loss DEL dbSNP153 1..33 33 - - - 55866 RMVar_ID_55866 Human_SNP_ID_218574051 m1A Human chr5 + 85479 85419 85479 TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACATACGCAGGAGGGAGG _________________________________GAGGCAGCGAGCAGACATACGCAGGAGGGAGG GGAGGCAGGGTGGTCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:85477..85568 26863196 MeRIP-seq:(Medium) rs1560883505 Functional Loss DEL dbSNP153 1..33 33 - - - 55867 RMVar_ID_55867 Human_SNP_ID_218574117 m1A Human chr5 + 85464 85464 85464 TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCGGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:85406..85566 26863196 MeRIP-seq:(Medium) rs146219474 Functional Loss SNV dbSNP153 33..33 33 - - - 55868 RMVar_ID_55868 Human_SNP_ID_218574135 m1A Human chr5 + 85479 85479 85479 TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACATACGCAGGAGGGAGG TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGGGAGGCAGCGAGCAGACATACGCAGGAGGGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:85477..85568 26863196 MeRIP-seq:(Medium) rs117925003 Functional Loss SNV dbSNP153 33..33 33 - - - 55869 RMVar_ID_55869 Human_SNP_ID_218576009 m1A Human chr5 - 92226 92226 92226 CCCGCCGTCTGCTGTGCTGAAACCCATGCTGGACCCTGGTCTCCCGAACTCCGACGCTTTCCCCG CCCGCCGTCTGCTGTGCTGAAACCCATGCTGGCCCCTGGTCTCCCGAACTCCGACGCTTTCCCCG T G HSALNG0039416 RNACentral:URS0000E9F88D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:91994..92322 26863196 MeRIP-seq:(Medium) rs58960904 Functional Loss SNV dbSNP153 33..33 33 - - - 55870 RMVar_ID_55870 Human_SNP_ID_218576757 m1A Human chr5 + 94559 94559 94559 GGTTCTGGGCCTGGGAATCTGGGCAGGGGGAGAGTGAAGAGGGGTAGGCTGGGATGAGTGGCTGG GGTTCTGGGCCTGGGAATCTGGGCAGGGGGAGGGTGAAGAGGGGTAGGCTGGGATGAGTGGCTGG A G PLEKHG4B Ensembl:ENSG00000153404 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:94556..94639 26863196 MeRIP-seq:(Medium) rs1224642450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229926 55871 RMVar_ID_55871 Human_SNP_ID_218589942 m1A Human chr5 + 142395 142392 142395 GTTCCACATACGACACGCACACAGAATCACACAACACACACAGTCACATGCCTCACACGATACAC GTTCCACATACGACACGCACACAGAATCAC___ACACACACAGTCACATGCCTCACACGATACAC CACA C PLEKHG4B Ensembl:ENSG00000153404 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:142348..142474 26863196 MeRIP-seq:(Medium) rs535740188 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_283840 55872 RMVar_ID_55872 Human_SNP_ID_218589943 m1A Human chr5 + 142395 142394 142395 GTTCCACATACGACACGCACACAGAATCACACAACACACACAGTCACATGCCTCACACGATACAC GTTCCACATACGACACGCACACAGAATCACAC_ACACACACAGTCACATGCCTCACACGATACAC CA C PLEKHG4B Ensembl:ENSG00000153404 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:142348..142474 26863196 MeRIP-seq:(Medium) rs1553986325 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_283840 55873 RMVar_ID_55873 Human_SNP_ID_218604963 m1A Human chr5 - 190445 190441 190445 CAGAGACTGAGGGAGAGAGAAAGGGAAACAGAAAGAGACAGACTGAGAGAGAGACAGAAAGGGAG CAGAGACTGAGGGAGAGAGAAAGGGAAACAGA____GACAGACTGAGAGAGAGACAGAAAGGGAG CTCTT C lnc-CCDC127-3,lnc-CCDC127-3:2,lnc-CCDC127-3:3 RNACentral:URS00008BCB82,RNACentral:URS00009B2EFE,RNACentral:URS00008C1537 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:190394..190553 26863196 MeRIP-seq:(Medium) rs1203121503 Functional Loss DEL dbSNP153 33..36 33 - - - 55874 RMVar_ID_55874 Human_SNP_ID_218608147 m1A Human chr5 - 197803 197803 197803 CAGGGACCACTGGGGTGGGGACACACTCCGGGAGGGGGTGATACGGGGCAGCGGTGTAGGGAAAA CAGGGACCACTGGGGTGGGGACACACTCCGGGGGGGGGTGATACGGGGCAGCGGTGTAGGGAAAA T C CCDC127 Ensembl:ENSG00000164366 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:197709..197913 26863196 MeRIP-seq:(Medium) rs1408037259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783037,Human_RBP_ID_8212970,Human_RBP_ID_9436823 55875 RMVar_ID_55875 Human_SNP_ID_218608157 m1A Human chr5 + 197820 197820 197820 CCCCGTATCACCCCCTCCCGGAGTGTGTCCCCACCCCAGTGGTCCCTGTGTCACCCCCTCCCCGA CCCCGTATCACCCCCTCCCGGAGTGTGTCCCCCCCCCAGTGGTCCCTGTGTCACCCCCTCCCCGA A C RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:197769..197929 26863196 MeRIP-seq:(Medium) rs1379089276 Functional Loss SNV dbSNP153 33..33 33 - - - 55876 RMVar_ID_55876 Human_SNP_ID_218609527 m1A Human chr5 - 202799 202799 202799 GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCACGTTTGTCTTTAAATGAAGAAAACACAGTCAG GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCTCGTTTGTCTTTAAATGAAGAAAACACAGTCAG T A CCDC127 Ensembl:ENSG00000164366 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7736361 Functional Loss SNV dbSNP153 33..33 33 - - - 55877 RMVar_ID_55877 Human_SNP_ID_218609528 m1A Human chr5 - 202799 202799 202799 GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCACGTTTGTCTTTAAATGAAGAAAACACAGTCAG GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCGCGTTTGTCTTTAAATGAAGAAAACACAGTCAG T C CCDC127 Ensembl:ENSG00000164366 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7736361 Functional Loss SNV dbSNP153 33..33 33 - - - 55878 RMVar_ID_55878 Human_SNP_ID_218610118 m1A Human chr5 + 205100 205100 205100 GCTTCAAGAAACCATATCCCCAACAGCGGCAGAGCATCGGGAGGAGACCCTCTGTCTCTGAGGCT GCTTCAAGAAACCATATCCCCAACAGCGGCAGGGCATCGGGAGGAGACCCTCTGTCTCTGAGGCT A G RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:205051..205250 32194978 MeRIP-seq:(Medium) rs1398614795 Functional Loss SNV dbSNP153 33..33 33 - - - 55879 RMVar_ID_55879 Human_SNP_ID_218610213 m1A Human chr5 - 205380 205378 205380 GGAACACCAACAAACGCCAGAATGGCAGACTCATGTGGCTCTATCTCAAATACTGGGAACTCGTT GGAACACCAACAAACGCCAGAATGGCAGACTC__GTGGCTCTATCTCAAATACTGGGAACTCGTT CAT C CCDC127 Ensembl:ENSG00000164366 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:205351..205492 26863196 MeRIP-seq:(Medium) rs755461135 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_27515303 Human_miRNA_ID_2946991 RMVar_hsa_circ_111247,RMVar_hsa_circ_229929 55880 RMVar_ID_55880 Human_SNP_ID_218610260 m1A Human chr5 + 205493 205493 205493 CTGCCATCTCTAGGTCAGCGGCGACGGGGTCGACGGACGCTCGCACCAGTAAGCTCTTCTCTATC CTGCCATCTCTAGGTCAGCGGCGACGGGGTCGGCGGACGCTCGCACCAGTAAGCTCTTCTCTATC A G RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:205444..205511 26863196 MeRIP-seq:(Medium) rs1372779453 Functional Loss SNV dbSNP153 33..33 33 - - - 55881 RMVar_ID_55881 Human_SNP_ID_218613557 m1A Human chr5 + 218128 218128 218128 GGTCGGGGAGCGCGGGACCTCAGCGTTCCCTTAACGCCACCGTCCGCGGGTCCGCTTTGCGCAGG GGTCGGGGAGCGCGGGACCTCAGCGTTCCCTTTACGCCACCGTCCGCGGGTCCGCTTTGCGCAGG A T RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:218039..218150 26863196 MeRIP-seq:(Medium) rs1243045862 Functional Loss SNV dbSNP153 33..33 33 - - - 55882 RMVar_ID_55882 Human_SNP_ID_218613689 m1A Human chr5 + 218352 218352 218352 AGGGACTGGCGGGACTGCGCGGCGGCAACAGCAGACATGTCGGGGGTCCGGGGCCTGTCGCGGCT AGGGACTGGCGGGACTGCGCGGCGGCAACAGCGGACATGTCGGGGGTCCGGGGCCTGTCGCGGCT A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding 5'UTR,5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs377134185 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_77485,Human_RBP_ID_838841,Human_RBP_ID_4828274,Human_RBP_ID_9306371,Human_RBP_ID_9335552,Human_RBP_ID_18056687,Human_RBP_ID_18840894,Human_RBP_ID_22458775 Human_Splice_Rec_630723,Human_Splice_Rec_630745,Human_Splice_Rec_630769,Human_Splice_Rec_630773,Human_Splice_Rec_630797,Human_Splice_Rec_630823,Human_Splice_Rec_630851,Human_Splice_Rec_630859,Human_Splice_Rec_630961 Clinvar_Rec_145 55883 RMVar_ID_55883 Human_SNP_ID_218613690 m1A Human chr5 + 218352 218352 218352 AGGGACTGGCGGGACTGCGCGGCGGCAACAGCAGACATGTCGGGGGTCCGGGGCCTGTCGCGGCT AGGGACTGGCGGGACTGCGCGGCGGCAACAGCTGACATGTCGGGGGTCCGGGGCCTGTCGCGGCT A T SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding 5'UTR,5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs377134185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77485,Human_RBP_ID_838841,Human_RBP_ID_4828274,Human_RBP_ID_9306371,Human_RBP_ID_9335552,Human_RBP_ID_18056687,Human_RBP_ID_18840894,Human_RBP_ID_22458775 Human_Splice_Rec_630723,Human_Splice_Rec_630745,Human_Splice_Rec_630769,Human_Splice_Rec_630773,Human_Splice_Rec_630797,Human_Splice_Rec_630823,Human_Splice_Rec_630851,Human_Splice_Rec_630859,Human_Splice_Rec_630961 Clinvar_Rec_145 55884 RMVar_ID_55884 Human_SNP_ID_218613723 m1A Human chr5 - 218377 218377 218377 CAGCGCCAGGCGCCGAGCGCTCAGCAGCCGCGACAGGCCCCGGACCCCCGACATGTCTGCTGTTG CAGCGCCAGGCGCCGAGCGCTCAGCAGCCGCGGCAGGCCCCGGACCCCCGACATGTCTGCTGTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:218301..218461;chr5:218301..218668;chr5:218301..218669;chr5:218301..218488 26863196 MeRIP-seq:(Medium) rs768328967 Functional Loss SNV dbSNP153 33..33 33 - - - 55885 RMVar_ID_55885 Human_SNP_ID_218615071 m1A Human chr5 + 223531 223531 223531 AACAGGAACCCGAGGTTTTCACTTCACTGTTGATGGGAACAAGAGGGCATCTGCTAAAGTTTCAG AACAGGAACCCGAGGTTTTCACTTCACTGTTGTTGGGAACAAGAGGGCATCTGCTAAAGTTTCAG A T SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:223476..223550 26863196 MeRIP-seq:(Medium) rs34635677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73831,Human_RBP_ID_249827,Human_RBP_ID_946525,Human_RBP_ID_1653069,Human_RBP_ID_1994063,Human_RBP_ID_2923380,Human_RBP_ID_4846268,Human_RBP_ID_5610777,Human_RBP_ID_8943824,Human_RBP_ID_18056690,Human_RBP_ID_18840898,Human_RBP_ID_22459468 Human_Splice_Rec_630724,Human_Splice_Rec_630725,Human_Splice_Rec_630746,Human_Splice_Rec_630747,Human_Splice_Rec_630770,Human_Splice_Rec_630771,Human_Splice_Rec_630774,Human_Splice_Rec_630775,Human_Splice_Rec_630798,Human_Splice_Rec_630799,Human_Splice_Rec_630824,Human_Splice_Rec_630825,Human_Splice_Rec_630854,Human_Splice_Rec_630855,Human_Splice_Rec_630860,Human_Splice_Rec_630861,Human_Splice_Rec_630962,Human_Splice_Rec_630963 Human_miRNA_ID_2586457 Clinvar_Rec_146 GWAS_ID_6658 RMVar_hsa_circ_47809,RMVar_hsa_circ_318776,RMVar_hsa_circ_375563,RMVar_hsa_circ_347448,RMVar_hsa_circ_92161,RMVar_hsa_circ_229931,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_229930 55886 RMVar_ID_55886 Human_SNP_ID_218615328 m1A Human chr5 - 224462 224461 224462 AGGAAACAGCTTGGTAACACATGCTGTATTAAACCCTGCCTCAGAAAGGCCAAATGCAGCTCGCA AGGAAACAGCTTGGTAACACATGCTGTATTAA_CCCTGCCTCAGAAAGGCCAAATGCAGCTCGCA GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:224351..224577 26863196 MeRIP-seq:(Medium) rs760710175 Functional Loss DEL dbSNP153 33..33 33 - - - 55887 RMVar_ID_55887 Human_SNP_ID_218615332 m1A Human chr5 + 224465 224465 224465 GAGCTGCATTTGGCCTTTCTGAGGCAGGGTTTAATACAGCATGTGTTACCAAGCTGTTTCCTACC GAGCTGCATTTGGCCTTTCTGAGGCAGGGTTTGATACAGCATGTGTTACCAAGCTGTTTCCTACC A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:224376..224500 32194978 MeRIP-seq:(Medium) rs200519133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73833,Human_RBP_ID_1653073,Human_RBP_ID_5121290,Human_RBP_ID_7426578,Human_RBP_ID_18056691,Human_RBP_ID_22459469 Human_Splice_Rec_630727,Human_Splice_Rec_630749,Human_Splice_Rec_630777,Human_Splice_Rec_630801,Human_Splice_Rec_630827,Human_Splice_Rec_630857,Human_Splice_Rec_630863,Human_Splice_Rec_630965 RMVar_hsa_circ_47809,RMVar_hsa_circ_318776,RMVar_hsa_circ_375563,RMVar_hsa_circ_347448,RMVar_hsa_circ_92161,RMVar_hsa_circ_229931,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_229930 55888 RMVar_ID_55888 Human_SNP_ID_218615446 m1A Human chr5 + 224799 224799 224799 CTTGCCTACTACCTTCCCCACCTACCCCCGCCACCCCAACACCTTAAGAAAAGGAGATCACCTAA CTTGCCTACTACCTTCCCCACCTACCCCCGCCCCCCCAACACCTTAAGAAAAGGAGATCACCTAA A C SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:224794..225640 32194978 MeRIP-seq:(Medium) rs1261220781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47809,RMVar_hsa_circ_318776,RMVar_hsa_circ_375563,RMVar_hsa_circ_347448,RMVar_hsa_circ_92161,RMVar_hsa_circ_229931,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_229930 55889 RMVar_ID_55889 Human_SNP_ID_218615865 m1A Human chr5 - 225999 225999 225999 TGCAATAGCGAGTGGCCAGTCCGATCAGCCACACAGCAGCACCGATGGGCCTGCCCGCCCTTTCC TGCAATAGCGAGTGGCCAGTCCGATCAGCCACGCAGCAGCACCGATGGGCCTGCCCGCCCTTTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:225926..226025 32194978 MeRIP-seq:(Medium) rs765111856 Functional Loss SNV dbSNP153 33..33 33 - - - 55890 RMVar_ID_55890 Human_SNP_ID_218616579 m1A Human chr5 + 228302 228302 228302 CACTGTGCATAGAGGACGGGTCCATCCATCGCATAAGAGCAAAGAACACTGTTGTTGCCACAGGG CACTGTGCATAGAGGACGGGTCCATCCATCGCGTAAGAGCAAAGAACACTGTTGTTGCCACAGGG A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:228251..231000 32194978 MeRIP-seq:(Medium) rs571292356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640783,Human_RBP_ID_3967064,Human_RBP_ID_22459472,Human_RBP_ID_26826125 Human_Splice_Rec_630755,Human_Splice_Rec_630783,Human_Splice_Rec_630805,Human_Splice_Rec_630833,Human_Splice_Rec_630869,Human_Splice_Rec_630877,Human_Splice_Rec_630879,Human_Splice_Rec_630899,Human_Splice_Rec_630971 Clinvar_Rec_147 RMVar_hsa_circ_16451,RMVar_hsa_circ_47809,RMVar_hsa_circ_375563,RMVar_hsa_circ_347448,RMVar_hsa_circ_92161,RMVar_hsa_circ_126360,RMVar_hsa_circ_229931,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_331462,RMVar_hsa_circ_9468,RMVar_hsa_circ_54742,RMVar_hsa_circ_229934,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_346530,RMVar_hsa_circ_64612,RMVar_hsa_circ_229935,RMVar_hsa_circ_76608,RMVar_hsa_circ_107608,RMVar_hsa_circ_363481,RMVar_hsa_circ_229936 55891 RMVar_ID_55891 Human_SNP_ID_218617358 m1A Human chr5 - 230924 230924 230924 CCTGCCCTGGTGATCATGGCCGTGCCGTCGCCAGTGCTGGTGTGGGCAGACGTGCAGCTGAAGTA CCTGCCCTGGTGATCATGGCCGTGCCGTCGCCGGTGCTGGTGTGGGCAGACGTGCAGCTGAAGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:230819..231004 26863196 MeRIP-seq:(Medium) rs1041947 Functional Loss SNV dbSNP153 33..33 33 - - - 55892 RMVar_ID_55892 Human_SNP_ID_218617379 m1A Human chr5 + 230946 230946 230946 ACACCAGCACTGGCGACGGCACGGCCATGATCACCAGGGCAGGCCTTCCTTGCCAGGACCTAGAG ACACCAGCACTGGCGACGGCACGGCCATGATCGCCAGGGCAGGCCTTCCTTGCCAGGACCTAGAG A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:230828..230953 26863196 MeRIP-seq:(Medium) rs772325115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249833,Human_RBP_ID_4854352,Human_RBP_ID_22458779 Human_Splice_Rec_630729,Human_Splice_Rec_630756,Human_Splice_Rec_630757,Human_Splice_Rec_630784,Human_Splice_Rec_630785,Human_Splice_Rec_630806,Human_Splice_Rec_630807,Human_Splice_Rec_630834,Human_Splice_Rec_630835,Human_Splice_Rec_630870,Human_Splice_Rec_630871,Human_Splice_Rec_630878,Human_Splice_Rec_630880,Human_Splice_Rec_630881,Human_Splice_Rec_630900,Human_Splice_Rec_630901,Human_Splice_Rec_630903,Human_Splice_Rec_630907,Human_Splice_Rec_630972,Human_Splice_Rec_630973 Clinvar_Rec_148 RMVar_hsa_circ_16451,RMVar_hsa_circ_47809,RMVar_hsa_circ_375563,RMVar_hsa_circ_92161,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_331462,RMVar_hsa_circ_9468,RMVar_hsa_circ_54742,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_346530,RMVar_hsa_circ_64612,RMVar_hsa_circ_123139,RMVar_hsa_circ_107608,RMVar_hsa_circ_363481,RMVar_hsa_circ_229936,RMVar_hsa_circ_316177,RMVar_hsa_circ_316737,RMVar_hsa_circ_326619,RMVar_hsa_circ_303216,RMVar_hsa_circ_229937,RMVar_hsa_circ_229938 55893 RMVar_ID_55893 Human_SNP_ID_218618624 m1A Human chr5 - 235128 235128 235128 TCTCAGGGCCACAGCCTCTGGTAAGACAGAACACCATCACATACGGCAGAGAACGGCAACGGCAG TCTCAGGGCCACAGCCTCTGGTAAGACAGAACGCCATCACATACGGCAGAGAACGGCAACGGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:235126..235445 32194978 MeRIP-seq:(Medium) rs765268601 Functional Loss SNV dbSNP153 33..33 33 - - - 55894 RMVar_ID_55894 Human_SNP_ID_218618625 m1A Human chr5 - 235128 235128 235128 TCTCAGGGCCACAGCCTCTGGTAAGACAGAACACCATCACATACGGCAGAGAACGGCAACGGCAG TCTCAGGGCCACAGCCTCTGGTAAGACAGAACCCCATCACATACGGCAGAGAACGGCAACGGCAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:235126..235445 32194978 MeRIP-seq:(Medium) rs765268601 Functional Loss SNV dbSNP153 33..33 33 - - - 55895 RMVar_ID_55895 Human_SNP_ID_218623130 m1A Human chr5 - 251069 251069 251069 CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCATAGAGCTTGCTGATTTTCCCACAACCTTCTTG CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCGTAGAGCTTGCTGATTTTCCCACAACCTTCTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:251026..251405 32194978 MeRIP-seq:(Medium) rs747249998 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_149,Clinvar_Rec_150 55896 RMVar_ID_55896 Human_SNP_ID_218623131 m1A Human chr5 - 251069 251069 251069 CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCATAGAGCTTGCTGATTTTCCCACAACCTTCTTG CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCCTAGAGCTTGCTGATTTTCCCACAACCTTCTTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:251026..251405 32194978 MeRIP-seq:(Medium) rs747249998 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_149,Clinvar_Rec_150 55897 RMVar_ID_55897 Human_SNP_ID_218624257 m1A Human chr5 - 254342 254342 254342 TCACGTTTCTTATTACTCTAACAGAGCAATACAGAAAAAACACAGCAGACATTAACATGATCTAA TCACGTTTCTTATTACTCTAACAGAGCAATACGGAAAAAACACAGCAGACATTAACATGATCTAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:254339..254420 26863196 MeRIP-seq:(Medium) rs371773898 Functional Loss SNV dbSNP153 33..33 33 - - - 55898 RMVar_ID_55898 Human_SNP_ID_218625745 m1A Human chr5 - 258236 258234 258236 ACATGGGGCGGAGCTCACAGTAATGCTCTGACAGGGGGCGGAGCTCACGGTAATGCTCTGGCAGG ACATGGGGCGGAGCTCACAGTAATGCTCTGAC__GGGGCGGAGCTCACGGTAATGCTCTGGCAGG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:258186..258313 26863196 MeRIP-seq:(Medium) rs1191838293 Functional Loss DEL dbSNP153 33..34 33 - - - 55899 RMVar_ID_55899 Human_SNP_ID_218625746 m1A Human chr5 - 258236 258235 258236 ACATGGGGCGGAGCTCACAGTAATGCTCTGACAGGGGGCGGAGCTCACGGTAATGCTCTGGCAGG ACATGGGGCGGAGCTCACAGTAATGCTCTGAC_GGGGGCGGAGCTCACGGTAATGCTCTGGCAGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:258186..258313 26863196 MeRIP-seq:(Medium) rs199499813 Functional Loss DEL dbSNP153 33..33 33 - - - 55900 RMVar_ID_55900 Human_SNP_ID_218625749 m1A Human chr5 - 258236 258236 258236 ACATGGGGCGGAGCTCACAGTAATGCTCTGACAGGGGGCGGAGCTCACGGTAATGCTCTGGCAGG ACATGGGGCGGAGCTCACAGTAATGCTCTGACGGGGGGCGGAGCTCACGGTAATGCTCTGGCAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:258186..258313 26863196 MeRIP-seq:(Medium) rs1261262207 Functional Loss SNV dbSNP153 33..33 33 - - - 55901 RMVar_ID_55901 Human_SNP_ID_218626024 m1A Human chr5 - 258568 258568 258568 AGCTCACACGGTAATGCTCTGGCGGGGGGCGGAGCTCACGGCAAGGCTCTGAGAGGAGAAGGAGC AGCTCACACGGTAATGCTCTGGCGGGGGGCGGCGCTCACGGCAAGGCTCTGAGAGGAGAAGGAGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr5:258250..258609;chr5:258529..258612 26863196 MeRIP-seq:(Medium) rs1335303259 Functional Loss SNV dbSNP153 33..33 33 - - - 55902 RMVar_ID_55902 Human_SNP_ID_218627657 m1A Human chr5 + 262358 262358 262358 ATTACCGTGTGAGCTCCGCCTCCCGGCAGAGCATTACCGTGTGAGCTCCGCCTCCTGTCCAAGCA ATTACCGTGTGAGCTCCGCCTCCCGGCAGAGCGTTACCGTGTGAGCTCCGCCTCCTGTCCAAGCA A G AC021087.5 Ensembl:ENSG00000286001 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:262256..262388 26863196 MeRIP-seq:(Medium) rs1230100177 Functional Loss SNV dbSNP153 33..33 33 - - - 55903 RMVar_ID_55903 Human_SNP_ID_218630243 m1A Human chr5 + 271698 271698 271698 CCTGAGAGGTCTCTCGTCGCTGCAGGCGCCTCAGCCCAGCCGCGTGCCTTGGCCCATGGCCGCCT CCTGAGAGGTCTCTCGTCGCTGCAGGCGCCTCGGCCCAGCCGCGTGCCTTGGCCCATGGCCGCCT A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding 5'UTR,3'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:271651..271725;chr5:271651..271750 26863196 MeRIP-seq:(Medium) rs759142062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77328,Human_RBP_ID_166131,Human_RBP_ID_250515,Human_RBP_ID_640820,Human_RBP_ID_4828387 Human_miRNA_ID_1963708,Human_miRNA_ID_2391661,Human_miRNA_ID_2491223,Human_miRNA_ID_2553069,Human_miRNA_ID_2763149 RMVar_hsa_circ_114576,RMVar_hsa_circ_229942 55904 RMVar_ID_55904 Human_SNP_ID_218630247 m1A Human chr5 + 271703 271703 271703 GAGGTCTCTCGTCGCTGCAGGCGCCTCAGCCCAGCCGCGTGCCTTGGCCCATGGCCGCCTACTCT GAGGTCTCTCGTCGCTGCAGGCGCCTCAGCCCGGCCGCGTGCCTTGGCCCATGGCCGCCTACTCT A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding 5'UTR,3'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:271626..271911 26863196 MeRIP-seq:(Medium) rs192942671 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_77328,Human_RBP_ID_166131,Human_RBP_ID_640820,Human_RBP_ID_4828387 Human_miRNA_ID_1963708,Human_miRNA_ID_2391661,Human_miRNA_ID_2491223,Human_miRNA_ID_2553069,Human_miRNA_ID_2763149 Clinvar_Rec_151 RMVar_hsa_circ_114576,RMVar_hsa_circ_229942 55905 RMVar_ID_55905 Human_SNP_ID_218630325 m1A Human chr5 - 271813 271813 271813 TGCCCGGGCGGTGCCAGGCCGCACCTCTGGAAAACGTTCCACAGGAAGCTCTGGTCCGGCAGCGC TGCCCGGGCGGTGCCAGGCCGCACCTCTGGAATACGTTCCACAGGAAGCTCTGGTCCGGCAGCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:271651..271969 26863196 MeRIP-seq:(Medium) rs762870078 Functional Loss SNV dbSNP153 33..33 33 - - - 55906 RMVar_ID_55906 Human_SNP_ID_218630326 m1A Human chr5 - 271813 271813 271813 TGCCCGGGCGGTGCCAGGCCGCACCTCTGGAAAACGTTCCACAGGAAGCTCTGGTCCGGCAGCGC TGCCCGGGCGGTGCCAGGCCGCACCTCTGGAAGACGTTCCACAGGAAGCTCTGGTCCGGCAGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:271651..271969 26863196 MeRIP-seq:(Medium) rs762870078 Functional Loss SNV dbSNP153 33..33 33 - - - 55907 RMVar_ID_55907 Human_SNP_ID_218632562 m1A Human chr5 + 278683 278683 278683 TGCAGTAAACCGAGATCGTGCCATTGCACTCCAGCCTGGGTGACAGAGCCAGACCCTGTCTCAAA TGCAGTAAACCGAGATCGTGCCATTGCACTCCGGCCTGGGTGACAGAGCCAGACCCTGTCTCAAA A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:278632..278757 26863196 MeRIP-seq:(Medium) rs953389745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940 55908 RMVar_ID_55908 Human_SNP_ID_218633215 m1A Human chr5 - 280489 280489 280489 AGCCCACAGTGCCCAGCACAGCCCTGCCCTCTACTTCGGTCTATGGTCTCCCCTCTTAAATTCCA AGCCCACAGTGCCCAGCACAGCCCTGCCCTCTGCTTCGGTCTATGGTCTCCCCTCTTAAATTCCA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:280391..280565 26863196 MeRIP-seq:(Medium) rs1180635216 Functional Loss SNV dbSNP153 33..33 33 - - - 55909 RMVar_ID_55909 Human_SNP_ID_218633729 m1A Human chr5 + 282026 282026 282026 GAGGAGCTGATATTCTAGTTTGAGGGCCCTGCAGCTGGAGATACAGATAGGAGCTGATGTTGTAG GAGGAGCTGATATTCTAGTTTGAGGGCCCTGCGGCTGGAGATACAGATAGGAGCTGATGTTGTAG A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:281976..282109 26863196 MeRIP-seq:(Medium) rs915595550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838303,Human_RBP_ID_15419735 RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940 55910 RMVar_ID_55910 Human_SNP_ID_218634579 m1A Human chr5 - 284531 284531 284531 TGGGTCTCAAACTGCATGGCCCTCAAACTGGAACATCTTCTCCCCCGCACAGGTCTCCAGTTGCA TGGGTCTCAAACTGCATGGCCCTCAAACTGGAGCATCTTCTCCCCCGCACAGGTCTCCAGTTGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:284480..284753 26863196 MeRIP-seq:(Medium) rs1472565174 Functional Loss SNV dbSNP153 33..33 33 - - - 55911 RMVar_ID_55911 Human_SNP_ID_218635160 m1A Human chr5 - 286224 286224 286224 AAACTAGAACATCAGCTCCCGCCCAGGTCGCCAGCTGCACCACCCTCAAACCGGAACATCAGCTC AAACTAGAACATCAGCTCCCGCCCAGGTCGCCGGCTGCACCACCCTCAAACCGGAACATCAGCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:286176..286350 26863196 MeRIP-seq:(Medium) rs563019827 Functional Loss SNV dbSNP153 33..33 33 - - - 55912 RMVar_ID_55912 Human_SNP_ID_218635171 m1A Human chr5 - 286263 286262 286264 ACATCAGCTCCCCGCTGGGTCTCCAGCTGCACAGTCCTCAAACTAGAACATCAGCTCCCGCCCAG ACATCAGCTCCCCGCTGGGTCTCCAGCTGCA__GTCCTCAAACTAGAACATCAGCTCCCGCCCAG CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:286222..286318 26863196 MeRIP-seq:(Medium) rs752101365 Functional Loss DEL dbSNP153 32..33 33 - - - 55913 RMVar_ID_55913 Human_SNP_ID_218636866 m1A Human chr5 + 292647 292647 292647 TATGGCAAAGATGGGTTTGAATCCACCAGGATAAATGTGCAGGATCTCCTCTCTGGTGGGAGAAG TATGGCAAAGATGGGTTTGAATCCACCAGGATGAATGTGCAGGATCTCCTCTCTGGTGGGAGAAG A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:292637..292914 26863196 MeRIP-seq:(Medium) rs1243958580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15419923,Human_RBP_ID_26350592,Human_RBP_ID_27574108 RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940 55914 RMVar_ID_55914 Human_SNP_ID_218636869 m1A Human chr5 - 292661 292661 292661 ATCCCTCTCTGTCTCTTCTCCCACCAGAGAGGAGATCCTGCACATTTATCCTGGTGGATTCAAAC ATCCCTCTCTGTCTCTTCTCCCACCAGAGAGGCGATCCTGCACATTTATCCTGGTGGATTCAAAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:292652..292816 26863196 MeRIP-seq:(Medium) rs1286467008 Functional Loss SNV dbSNP153 33..33 33 - - - 55915 RMVar_ID_55915 Human_SNP_ID_218636917 m1A Human chr5 - 292896 292896 292896 GCCAGGAGGTAAACCCTCAACCAAGGGCCTCTAGGTGTCCAAGGCCAAGTCTTGTTCAAGAGGTG GCCAGGAGGTAAACCCTCAACCAAGGGCCTCTGGGTGTCCAAGGCCAAGTCTTGTTCAAGAGGTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:292744..292909 26863196 MeRIP-seq:(Medium) rs1268557473 Functional Loss SNV dbSNP153 33..33 33 - - - 55916 RMVar_ID_55916 Human_SNP_ID_218640177 m1A Human chr5 + 302481 302393 302482 TCCCTGCATAACTGCTGGAGGGCGGGTCATGGAGTGCTGCTGCTGTGTGTGTGTGTGTGTGTGTG __________________________________TGCTGCTGCTGTGTGTGTGTGTGTGTGTGTG CTCTGTGTGTATGCCTCAGGTTCAGGTGCACCTGCCTTTGTGGGGAGAGCACAGCTTCCCTGCATAACTGCTGGAGGGCGGGTCATGGAG C AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:302475..302575 26863196 MeRIP-seq:(Medium) rs1561046909 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940 55917 RMVar_ID_55917 Human_SNP_ID_218641433 m1A Human chr5 + 306743 306743 306743 CTCCGGGATGATCGATAAGAACGAGCTGAAGCAGGCCCTCTCAGGTTTCGGTAACTCACTCACTC CTCCGGGATGATCGATAAGAACGAGCTGAAGCCGGCCCTCTCAGGTTTCGGTAACTCACTCACTC A C AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:306570..306797 26863196 MeRIP-seq:(Medium) rs755147828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640904,Human_RBP_ID_1994102,Human_RBP_ID_8613483,Human_RBP_ID_9398839,Human_RBP_ID_15420035,Human_RBP_ID_19124228 Human_Splice_Rec_631001,Human_Splice_Rec_631021,Human_Splice_Rec_631029,Human_Splice_Rec_631039,Human_Splice_Rec_631049,Human_Splice_Rec_631069,Human_Splice_Rec_631077,Human_Splice_Rec_631085 RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229944,RMVar_hsa_circ_80928,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_294234 55918 RMVar_ID_55918 Human_SNP_ID_218641434 m1A Human chr5 + 306743 306743 306743 CTCCGGGATGATCGATAAGAACGAGCTGAAGCAGGCCCTCTCAGGTTTCGGTAACTCACTCACTC CTCCGGGATGATCGATAAGAACGAGCTGAAGCGGGCCCTCTCAGGTTTCGGTAACTCACTCACTC A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:306570..306797 26863196 MeRIP-seq:(Medium) rs755147828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640904,Human_RBP_ID_1994102,Human_RBP_ID_8613483,Human_RBP_ID_9398839,Human_RBP_ID_15420035,Human_RBP_ID_19124228 Human_Splice_Rec_631001,Human_Splice_Rec_631021,Human_Splice_Rec_631029,Human_Splice_Rec_631039,Human_Splice_Rec_631049,Human_Splice_Rec_631069,Human_Splice_Rec_631077,Human_Splice_Rec_631085 RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229944,RMVar_hsa_circ_80928,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_294234 55919 RMVar_ID_55919 Human_SNP_ID_218642380 m1A Human chr5 - 309988 309933 309989 GGGGACGGCGGCCATCACTGGGGTGCACGGGCACGGCGGCCATCACTGGTGTGCACGGGGACGGC GGGGACGGCGGCCATCACTGGGGTGCACGGG__________________________________ CCCCGTGCACCCCAGTGATGGCCGCCGTCCCCGTGCACACCAGTGATGGCCGCCGTG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:309907..310075 26863196 MeRIP-seq:(Medium) rs1560864156 Functional Loss DEL dbSNP153 32..65 33 - - - 55920 RMVar_ID_55920 Human_SNP_ID_218642772 m1A Human chr5 - 311363 311363 311363 ACGATGCAGCCCTGGATGAAGTCGTCGAAGGCAATCTGCCCCCGTCCCTGCCTGTCAAACTTTCG ACGATGCAGCCCTGGATGAAGTCGTCGAAGGCGATCTGCCCCCGTCCCTGCCTGTCAAACTTTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:311315..311437 26863196 MeRIP-seq:(Medium) rs2244029 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_6659 55921 RMVar_ID_55921 Human_SNP_ID_218643445 m1A Human chr5 - 313909 313909 313909 GTCCAGGCCAGGTCAGCGGCAGAGACAGGGTGACCACCTACACTCCTGAAACAGGGATGGTTAAG GTCCAGGCCAGGTCAGCGGCAGAGACAGGGTGTCCACCTACACTCCTGAAACAGGGATGGTTAAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:313906..314003 26863196 MeRIP-seq:(Medium) rs1474319952 Functional Loss SNV dbSNP153 33..33 33 - - - 55922 RMVar_ID_55922 Human_SNP_ID_218643593 m1A Human chr5 - 314403 314403 314403 TGAATATATCCGTCAACCTCTGGGGAGAAAACAGGCATTTAAATCTCGATAGTAAATGGAAGGAG TGAATATATCCGTCAACCTCTGGGGAGAAAACGGGCATTTAAATCTCGATAGTAAATGGAAGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:314401..314650 32194978 MeRIP-seq:(Medium) rs1574220 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_6660,GWAS_ID_6661,GWAS_ID_6662 55923 RMVar_ID_55923 Human_SNP_ID_218643650 m1A Human chr5 + 314551 314551 314551 TGGCCTCTCGTGAAGAGCAGCACAACATGGAAAGAGCCAAAATGTCACAGTTCCTATCTGTGAGG TGGCCTCTCGTGAAGAGCAGCACAACATGGAAGGAGCCAAAATGTCACAGTTCCTATCTGTGAGG A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:314374..314648 26863196 MeRIP-seq:(Medium) rs199506819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640920,Human_RBP_ID_947163,Human_RBP_ID_9175874,Human_RBP_ID_17302591,Human_RBP_ID_18046867 RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_99688,RMVar_hsa_circ_229946,RMVar_hsa_circ_229947 55924 RMVar_ID_55924 Human_SNP_ID_218651611 m1A Human chr5 + 343969 343969 343969 GGAAGCGGAGGAGGCCCCTGCAGAAACAGTAAAGTATCCCGCCTTCTGCTTGTGTGGGTTGTTGC GGAAGCGGAGGAGGCCCCTGCAGAAACAGTAACGTATCCCGCCTTCTGCTTGTGTGGGTTGTTGC A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:343967..344392 26863196 MeRIP-seq:(Medium) rs746406348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1321383,Human_RBP_ID_5212769,Human_RBP_ID_8614554 Human_Splice_Rec_631098,Human_Splice_Rec_631102,Human_Splice_Rec_631122,Human_Splice_Rec_631144,Human_Splice_Rec_631160,Human_Splice_Rec_631161,Human_Splice_Rec_631170,Human_Splice_Rec_631180,Human_Splice_Rec_631186,Human_Splice_Rec_631192 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_338231,RMVar_hsa_circ_67941 55925 RMVar_ID_55925 Human_SNP_ID_218651989 m1A Human chr5 - 344697 344697 344697 GCCTCACACACACACCCCACACACAGCCCCCCACAGCCTCACACACACACACCCACACACACACA GCCTCACACACACACCCCACACACAGCCCCCCCCAGCCTCACACACACACACCCACACACACACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:344692..345136 26863196 MeRIP-seq:(Medium) rs1237558613 Functional Loss SNV dbSNP153 33..33 33 - - - 55926 RMVar_ID_55926 Human_SNP_ID_218652603 m1A Human chr5 - 345400 345397 345400 CACACCCACACACACACACAGCCAGGGACATCATCCGACACACACACACATCCCCACACACAGCC CACACCCACACACACACACAGCCAGGGACATC___CGACACACACACACATCCCCACACACAGCC GGAT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:345221..345643 26863196 MeRIP-seq:(Medium) rs1390599572 Functional Loss DEL dbSNP153 33..35 33 - - - 55927 RMVar_ID_55927 Human_SNP_ID_218654296 m1A Human chr5 - 352196 352196 352196 TTTAACCTCACAGTGACTGTCCCCTACAGCTGACCTATTTAACCATCACTGCACTGAAGCCACTT TTTAACCTCACAGTGACTGTCCCCTACAGCTGGCCTATTTAACCATCACTGCACTGAAGCCACTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:352194..352261 26863196 MeRIP-seq:(Medium) rs1463501392 Functional Loss SNV dbSNP153 33..33 33 - - - 55928 RMVar_ID_55928 Human_SNP_ID_218654706 m1A Human chr5 + 353774 353774 353774 GGGGGCAGAGAAGTCCAACCCCTCCAAGCGACACCGGGACCGCCTCAACGCCGAGTTGGACCACC GGGGGCAGAGAAGTCCAACCCCTCCAAGCGACGCCGGGACCGCCTCAACGCCGAGTTGGACCACC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding 5'UTR,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:343960..367816 32194978 MeRIP-seq:(Medium) rs1382035506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_631100,Human_Splice_Rec_631104,Human_Splice_Rec_631124,Human_Splice_Rec_631162,Human_Splice_Rec_631172,Human_Splice_Rec_631182,Human_Splice_Rec_631188,Human_Splice_Rec_631194 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_338231,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_337553,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55929 RMVar_ID_55929 Human_SNP_ID_218658255 m1A Human chr5 + 370086 370058 370086 CTGGTGCCCCATCCTCCCGGGCCCTCGCTGGAAGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCCC CTGGT____________________________GCCCCGTCCTCCCGGGCCCTCGCTGGAAGCCC TGCCCCATCCTCCCGGGCCCTCGCTGGAA T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:370026..370500;chr5:370026..370300 26863196 MeRIP-seq:(Medium) rs1560895006 Functional Loss DEL dbSNP153 6..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55930 RMVar_ID_55930 Human_SNP_ID_218658255 m1A Human chr5 + 370085 370058 370086 GCTGGTGCCCCATCCTCCCGGGCCCTCGCTGGAAGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCC GCTGGT____________________________GCCCCGTCCTCCCGGGCCCTCGCTGGAAGCC TGCCCCATCCTCCCGGGCCCTCGCTGGAA T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:369976..370150;chr5:370001..370150 26863196 MeRIP-seq:(Medium) rs1560895006 Functional Loss DEL dbSNP153 7..34 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55931 RMVar_ID_55931 Human_SNP_ID_218658273 m1A Human chr5 + 370085 370084 370085 GCTGGTGCCCCATCCTCCCGGGCCCTCGCTGGAAGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCC GCTGGTGCCCCATCCTCCCGGGCCCTCGCTGG_AGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCC GA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:369976..370150;chr5:370001..370150 26863196 MeRIP-seq:(Medium) rs544736764 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55932 RMVar_ID_55932 Human_SNP_ID_218658275 m1A Human chr5 + 370086 370086 370086 CTGGTGCCCCATCCTCCCGGGCCCTCGCTGGAAGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCCC CTGGTGCCCCATCCTCCCGGGCCCTCGCTGGATGCCCCGTCCTCCCGGGCCCTCGCTGGAAGCCC A T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:370026..370500;chr5:370026..370300 26863196 MeRIP-seq:(Medium) rs541334429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55933 RMVar_ID_55933 Human_SNP_ID_218658382 m1A Human chr5 - 370264 370264 370264 GAGTAAATGAGCAGAGCTTCCAGCGAGGGCCCAGGAGGTCGGGGCACCAGCGAGGGCCCGGGAGG GAGTAAATGAGCAGAGCTTCCAGCGAGGGCCCGGGAGGTCGGGGCACCAGCGAGGGCCCGGGAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:369976..370500 26863196 MeRIP-seq:(Medium) rs947733921 Functional Loss SNV dbSNP153 33..33 33 - - - 55934 RMVar_ID_55934 Human_SNP_ID_218658477 m1A Human chr5 + 370614 370613 370615 TAGGGGACAGCCCCCAGGAAGATGCAGGTGACAGGGGTGGGGTGGACAGCCCATGGGAAGGTGTG TAGGGGACAGCCCCCAGGAAGATGCAGGTGAC__GGGTGGGGTGGACAGCCCATGGGAAGGTGTG CAG C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:370576..370650 26863196 MeRIP-seq:(Medium) rs1387509383 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55935 RMVar_ID_55935 Human_SNP_ID_218658797 m1A Human chr5 - 372020 372020 372020 GTAAGGAATGTGGGTGCTTCATGAAGGTCCCTATTGGCAGGACTGCCTGCCTCTCTGCAGAGCCC GTAAGGAATGTGGGTGCTTCATGAAGGTCCCTGTTGGCAGGACTGCCTGCCTCTCTGCAGAGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:371972..372048 26863196 MeRIP-seq:(Medium) rs1442611424 Functional Loss SNV dbSNP153 33..33 33 - - - 55936 RMVar_ID_55936 Human_SNP_ID_218659115 m1A Human chr5 + 373423 373423 373423 GGCAGGGGACAGGTTGGCCTCTGCGGTCTTGGAGGCACAGAGCTCCTCCCGCCCTGGGCCTGTGG GGCAGGGGACAGGTTGGCCTCTGCGGTCTTGGGGGCACAGAGCTCCTCCCGCCCTGGGCCTGTGG A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:373373..373508 26863196 MeRIP-seq:(Medium) rs6894195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2291415,Human_miRNA_ID_2356758,Human_miRNA_ID_3059204 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55937 RMVar_ID_55937 Human_SNP_ID_218659309 m1A Human chr5 - 373938 373938 373938 CGGCATCGCGTGCCCCCCGCGGGCGCCCGCCCACTTCCCCCCTACTTCCCCCGCAGCCGCCGGCG CGGCATCGCGTGCCCCCCGCGGGCGCCCGCCCCCTTCCCCCCTACTTCCCCCGCAGCCGCCGGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:373936..374047 26863196 MeRIP-seq:(Medium) rs974249456 Functional Loss SNV dbSNP153 33..33 33 - - - 55938 RMVar_ID_55938 Human_SNP_ID_218659535 m1A Human chr5 + 374676 374676 374676 GAGACCAGGGAGGGAGGGGAACAGAGAGGCCGAGTCCCAAGGCCACCCGGTGCCACCGTCTCCGG GAGACCAGGGAGGGAGGGGAACAGAGAGGCCGGGTCCCAAGGCCACCCGGTGCCACCGTCTCCGG A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:374601..374725 26863196 MeRIP-seq:(Medium) rs1327547935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55939 RMVar_ID_55939 Human_SNP_ID_218660090 m1A Human chr5 + 376554 376553 376554 CGCGGGGAAACACAGGAAAGATGTGAATGAAGAAGAGTGGCCAGGCCAAGGGTTGGGGGTGCCTA CGCGGGGAAACACAGGAAAGATGTGAATGAATGAGAGTGGCCAGGCCAAGGGTTGGGGGTGCCTA GA TG AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:375803..376655;chr5:375951..376639;chr5:376076..376616 26863196 MeRIP-seq:(Medium) rs386684252 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_5655479 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55940 RMVar_ID_55940 Human_SNP_ID_218660094 m1A Human chr5 + 376554 376554 376554 CGCGGGGAAACACAGGAAAGATGTGAATGAAGAAGAGTGGCCAGGCCAAGGGTTGGGGGTGCCTA CGCGGGGAAACACAGGAAAGATGTGAATGAAGGAGAGTGGCCAGGCCAAGGGTTGGGGGTGCCTA A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:375803..376655;chr5:375951..376639;chr5:376076..376616 26863196 MeRIP-seq:(Medium) rs72711353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5655479 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_326897,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_280501,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_229949 55941 RMVar_ID_55941 Human_SNP_ID_218663286 m1A Human chr5 + 389959 389959 389959 GAGGGGGAGGGGAAGGGAGGGAGGGGGAGGGGAGACAGGACAGAGGCTGGAAAGGACAGTGATGC GAGGGGGAGGGGAAGGGAGGGAGGGGGAGGGGCGACAGGACAGAGGCTGGAAAGGACAGTGATGC A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:389951..390216 26863196 MeRIP-seq:(Medium) rs1261694814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22727313 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55942 RMVar_ID_55942 Human_SNP_ID_218663287 m1A Human chr5 + 389959 389959 389959 GAGGGGGAGGGGAAGGGAGGGAGGGGGAGGGGAGACAGGACAGAGGCTGGAAAGGACAGTGATGC GAGGGGGAGGGGAAGGGAGGGAGGGGGAGGGGGGACAGGACAGAGGCTGGAAAGGACAGTGATGC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:389951..390216 26863196 MeRIP-seq:(Medium) rs1261694814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22727313 RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55943 RMVar_ID_55943 Human_SNP_ID_218663292 m1A Human chr5 - 389974 389974 389974 CTGTCTGCATTCTGCGCATCACTGTCCTTTCCAGCCTCTGTCCTGTCTCCCCTCCCCCTCCCTCC CTGTCTGCATTCTGCGCATCACTGTCCTTTCCGGCCTCTGTCCTGTCTCCCCTCCCCCTCCCTCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:389951..390093 26863196 MeRIP-seq:(Medium) rs1393587073 Functional Loss SNV dbSNP153 33..33 33 - - - 55944 RMVar_ID_55944 Human_SNP_ID_218663293 m1A Human chr5 - 389974 389974 389974 CTGTCTGCATTCTGCGCATCACTGTCCTTTCCAGCCTCTGTCCTGTCTCCCCTCCCCCTCCCTCC CTGTCTGCATTCTGCGCATCACTGTCCTTTCCCGCCTCTGTCCTGTCTCCCCTCCCCCTCCCTCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:389951..390093 26863196 MeRIP-seq:(Medium) rs1393587073 Functional Loss SNV dbSNP153 33..33 33 - - - 55945 RMVar_ID_55945 Human_SNP_ID_218663679 m1A Human chr5 + 391357 391309 391357 GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA _________________________________GGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA GGGCCAGAGCGTGCACGGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:391240..391517;chr5:391227..391525 26863196 MeRIP-seq:(Medium) rs1560904053 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55946 RMVar_ID_55946 Human_SNP_ID_218663681 m1A Human chr5 + 391455 391309 391455 GGGGGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCACGGGGGCAGGGCGAGGC _________________________________GGGCCAGAGCGTGCACGGGGGCAGGGCGAGGC GGGCCAGAGCGTGCACGGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGAGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCACGGGGGCAGGGCGAGGCGGGCGCAGGGCGAGGCA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:391090..391525;chr5:390987..391536;chr5:390974..391525 26863196 MeRIP-seq:(Medium) rs1560904057 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55947 RMVar_ID_55947 Human_SNP_ID_218663688 m1A Human chr5 + 391357 391319 391357 GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA _________________________________GGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA GTGCACGGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:391240..391517;chr5:391227..391525 26863196 MeRIP-seq:(Medium) rs1560904076 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55948 RMVar_ID_55948 Human_SNP_ID_218663744 m1A Human chr5 + 391357 391356 391357 GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGC_GGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA CA C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:391240..391517;chr5:391227..391525 26863196 MeRIP-seq:(Medium) rs201631216 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55949 RMVar_ID_55949 Human_SNP_ID_218663748 m1A Human chr5 + 391357 391357 391357 GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA GGGCGCAGGGCGAGGCGGGCGCAGGGCGAGGCGGGGCCAGAGCGTGCATGGGCGCAGGGCGAGGA A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:391240..391517;chr5:391227..391525 26863196 MeRIP-seq:(Medium) rs964598114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55950 RMVar_ID_55950 Human_SNP_ID_218663851 m1A Human chr5 + 391455 391455 391455 GGGGGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCACGGGGGCAGGGCGAGGC GGGGGCAGGGCGAGGCGGGCGCAGGGCGAGGCGGGGCCAGAGCGTGCACGGGGGCAGGGCGAGGC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:391090..391525;chr5:390987..391536;chr5:390974..391525 26863196 MeRIP-seq:(Medium) rs1288334092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55951 RMVar_ID_55951 Human_SNP_ID_218664120 m1A Human chr5 + 392238 392238 392238 AGGGCCAGAGCGTGCACGGGCGCAGGGCGATGAGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCA AGGGCCAGAGCGTGCACGGGCGCAGGGCGATGCGGGCGCAGGGCGAGGCAGGGCCAGAGCGTGCA A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:392197..392300 26863196 MeRIP-seq:(Medium) rs1161682178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55952 RMVar_ID_55952 Human_SNP_ID_218664218 m1A Human chr5 + 392443 392443 392443 GCGTGCACGAACACACGGGTGCAGGGCGAGGCAGGCGCAGGGCGAGGCAGGGCCAGAGTGTGCAC GCGTGCACGAACACACGGGTGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGTGTGCAC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:392438..392547 26863196 MeRIP-seq:(Medium) rs1431855442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55953 RMVar_ID_55953 Human_SNP_ID_218665528 m1A Human chr5 - 397143 397143 397143 GTCAGGAGCTACGTGGATGGTCAGGGGCTAACATGGATGGTCAGGGGCTAACATGGATGGTCAGG GTCAGGAGCTACGTGGATGGTCAGGGGCTAACGTGGATGGTCAGGGGCTAACATGGATGGTCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:397003..397179;chr5:396976..397425;chr5:396879..397497 26863196 MeRIP-seq:(Medium) rs1486518648 Functional Loss SNV dbSNP153 33..33 33 - - - 55954 RMVar_ID_55954 Human_SNP_ID_218665638 m1A Human chr5 + 397391 397391 397391 CCCCTGACCATCCACGTAGCCCCTGACCATCCATGTTAGCCCCTGACCATCCCTGTTAGCCCCTG CCCCTGACCATCCACGTAGCCCCTGACCATCCCTGTTAGCCCCTGACCATCCCTGTTAGCCCCTG A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr5:397246..397432;chr5:396880..397505;chr5:396919..397450 26863196 MeRIP-seq:(Medium) rs1348079822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55955 RMVar_ID_55955 Human_SNP_ID_218665688 m1A Human chr5 - 397680 397509 397680 GGTCAGGGGCTACGTGGATGGTCAGGGGCTACATGGATGGTCAGGGGCTACGTGGATGGTCAGGG GGTCAGGGGCTACGTGGATGGTCAGGGGCTAC_________________________________ CGTAGCCCCTGACCGTCCACGTAGCTCCTGACCGTCCATGTTAGCCCCTGACCATGTTAGCCCCTGACCATCCCTGTTAGCCCCTGACCATCCACGTAGCTCCTGACCATCCATGTTAGCCCCTGACCATCCACATAGCCCCTGACCATCCACGTAGCCCCTGACCATCCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397626..397800 26863196 MeRIP-seq:(Medium) rs1560907105 Functional Loss DEL dbSNP153 33..65 33 - - - 55956 RMVar_ID_55956 Human_SNP_ID_218665730 m1A Human chr5 + 397634 397634 397634 ACGTAGCTCCTGACCATCCATGTTAGCCCCTGACCATCCACATAGCCCCTGACCATCCACGTAGC ACGTAGCTCCTGACCATCCATGTTAGCCCCTGCCCATCCACATAGCCCCTGACCATCCACGTAGC A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:397626..397801 26863196 MeRIP-seq:(Medium) rs1387876881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55957 RMVar_ID_55957 Human_SNP_ID_218665731 m1A Human chr5 + 397643 397643 397643 CTGACCATCCATGTTAGCCCCTGACCATCCACATAGCCCCTGACCATCCACGTAGCCCCTGACCA CTGACCATCCATGTTAGCCCCTGACCATCCACGTAGCCCCTGACCATCCACGTAGCCCCTGACCA A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:397637..397799 26863196 MeRIP-seq:(Medium) rs1276681722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55958 RMVar_ID_55958 Human_SNP_ID_218665732 m1A Human chr5 + 397643 397643 397643 CTGACCATCCATGTTAGCCCCTGACCATCCACATAGCCCCTGACCATCCACGTAGCCCCTGACCA CTGACCATCCATGTTAGCCCCTGACCATCCACTTAGCCCCTGACCATCCACGTAGCCCCTGACCA A T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:397637..397799 26863196 MeRIP-seq:(Medium) rs1276681722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55959 RMVar_ID_55959 Human_SNP_ID_218665735 m1A Human chr5 - 397680 397661 397680 GGTCAGGGGCTACGTGGATGGTCAGGGGCTACATGGATGGTCAGGGGCTACGTGGATGGTCAGGG GGTCAGGGGCTACGTGGATGGTCAGGGGCTAC___________________GTGGATGGTCAGGG CGTAGCCCCTGACCATCCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397626..397800 26863196 MeRIP-seq:(Medium) rs1340367006 Functional Loss DEL dbSNP153 33..51 33 - - - 55960 RMVar_ID_55960 Human_SNP_ID_218665741 m1A Human chr5 - 397680 397680 397680 GGTCAGGGGCTACGTGGATGGTCAGGGGCTACATGGATGGTCAGGGGCTACGTGGATGGTCAGGG GGTCAGGGGCTACGTGGATGGTCAGGGGCTACGTGGATGGTCAGGGGCTACGTGGATGGTCAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397626..397800 26863196 MeRIP-seq:(Medium) rs148426454 Functional Loss SNV dbSNP153 33..33 33 - - - 55961 RMVar_ID_55961 Human_SNP_ID_218665742 m1A Human chr5 - 397680 397680 397680 GGTCAGGGGCTACGTGGATGGTCAGGGGCTACATGGATGGTCAGGGGCTACGTGGATGGTCAGGG GGTCAGGGGCTACGTGGATGGTCAGGGGCTACCTGGATGGTCAGGGGCTACGTGGATGGTCAGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397626..397800 26863196 MeRIP-seq:(Medium) rs148426454 Functional Loss SNV dbSNP153 33..33 33 - - - 55962 RMVar_ID_55962 Human_SNP_ID_218665772 m1A Human chr5 - 397758 397757 397758 TGGTCAGGGGCTACGTGGACGGTCAGGGGCTAACATGGACGGTCAGGAGCTACGTGGACGGTCAG TGGTCAGGGGCTACGTGGACGGTCAGGGGCTA_CATGGACGGTCAGGAGCTACGTGGACGGTCAG GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:397626..398000 26863196 MeRIP-seq:(Medium) rs1376485097 Functional Loss DEL dbSNP153 33..33 33 - - - 55963 RMVar_ID_55963 Human_SNP_ID_218665827 m1A Human chr5 - 397895 397876 397895 TGGATGGTCAGGGGCTAACATGGATGGTCAGGAGCTACGTGGATGGTCAGGGGCTAACAGGGATG TGGATGGTCAGGGGCTAACATGGATGGTCAGG___________________GGCTAACAGGGATG CCCTGACCATCCACGTAGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397876..398441 26863196 MeRIP-seq:(Medium) rs1331568843 Functional Loss DEL dbSNP153 33..51 33 - - - 55964 RMVar_ID_55964 Human_SNP_ID_218665832 m1A Human chr5 - 397895 397886 397895 TGGATGGTCAGGGGCTAACATGGATGGTCAGGAGCTACGTGGATGGTCAGGGGCTAACAGGGATG TGGATGGTCAGGGGCTAACATGGATGGTCAGG_________GATGGTCAGGGGCTAACAGGGATG CCACGTAGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397876..398441 26863196 MeRIP-seq:(Medium) rs1276233363 Functional Loss DEL dbSNP153 33..41 33 - - - 55965 RMVar_ID_55965 Human_SNP_ID_218665839 m1A Human chr5 - 397895 397895 397895 TGGATGGTCAGGGGCTAACATGGATGGTCAGGAGCTACGTGGATGGTCAGGGGCTAACAGGGATG TGGATGGTCAGGGGCTAACATGGATGGTCAGGGGCTACGTGGATGGTCAGGGGCTAACAGGGATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:397876..398441 26863196 MeRIP-seq:(Medium) rs866046474 Functional Loss SNV dbSNP153 33..33 33 - - - 55966 RMVar_ID_55966 Human_SNP_ID_218665840 m1A Human chr5 + 397903 397899 397903 TTAGCCCCTGACCATCCACGTAGCTCCTGACCATCCATGTTAGCCCCTGACCATCCACGTAGCCC TTAGCCCCTGACCATCCACGTAGCTCCTG____TCCATGTTAGCCCCTGACCATCCACGTAGCCC GACCA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:397901..398437 26863196 MeRIP-seq:(Medium) rs1459116239 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55967 RMVar_ID_55967 Human_SNP_ID_218665841 m1A Human chr5 + 397903 397900 397904 TTAGCCCCTGACCATCCACGTAGCTCCTGACCATCCATGTTAGCCCCTGACCATCCACGTAGCCC TTAGCCCCTGACCATCCACGTAGCTCCTGA____CCATGTTAGCCCCTGACCATCCACGTAGCCC ACCAT A AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:397901..398437 26863196 MeRIP-seq:(Medium) rs1479309984 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55968 RMVar_ID_55968 Human_SNP_ID_218665842 m1A Human chr5 + 397903 397903 397903 TTAGCCCCTGACCATCCACGTAGCTCCTGACCATCCATGTTAGCCCCTGACCATCCACGTAGCCC TTAGCCCCTGACCATCCACGTAGCTCCTGACCGTCCATGTTAGCCCCTGACCATCCACGTAGCCC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:397901..398437 26863196 MeRIP-seq:(Medium) rs1176826201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55969 RMVar_ID_55969 Human_SNP_ID_218665859 m1A Human chr5 - 397937 397935 397937 TATGTGGATGGTCAGGGGCTACGTGGATGGTCAGGGGCTACGTGGATGGTCAGGGGCTAACATGG TATGTGGATGGTCAGGGGCTACGTGGATGGTC__GGGCTACGTGGATGGTCAGGGGCTAACATGG CCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:397651..398425 26863196 MeRIP-seq:(Medium) rs1308342904 Functional Loss DEL dbSNP153 33..34 33 - - - 55970 RMVar_ID_55970 Human_SNP_ID_218665932 m1A Human chr5 - 398102 398100 398102 ACGGTCAGGAGCTACGTGGATGGTCAGGAGCTACGTGGATGGTCAGGGGCTACGTGGATGGTCAG ACGGTCAGGAGCTACGTGGATGGTCAGGAGCT__GTGGATGGTCAGGGGCTACGTGGATGGTCAG CGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:397594..398430 26863196 MeRIP-seq:(Medium) rs1560907530 Functional Loss DEL dbSNP153 33..34 33 - - - 55971 RMVar_ID_55971 Human_SNP_ID_218665951 m1A Human chr5 - 398140 398139 398140 TGGTCAGGGGCTACGTGGATGGTCAGGGGCTAACATGGACGGTCAGGAGCTACGTGGATGGTCAG TGGTCAGGGGCTACGTGGATGGTCAGGGGCTA_CATGGACGGTCAGGAGCTACGTGGATGGTCAG GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:397641..398450 26863196 MeRIP-seq:(Medium) rs1162257323 Functional Loss DEL dbSNP153 33..33 33 - - - 55972 RMVar_ID_55972 Human_SNP_ID_218667130 m1A Human chr5 + 402177 402177 402177 AGACGCTTCTCCAAAGGAGACACAAAATGGCCAGTTTGTAGGTGGAAAGGTGCTCGGCATCGCCA AGACGCTTCTCCAAAGGAGACACAAAATGGCCCGTTTGTAGGTGGAAAGGTGCTCGGCATCGCCA A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:402171..402300 26863196 MeRIP-seq:(Medium) rs1203733856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55973 RMVar_ID_55973 Human_SNP_ID_218667264 m1A Human chr5 + 402548 402548 402548 GCAGTCGTTGATGAGGGTGTGGAGAGAAGGGGACCCTCGTGCACTGTTGGCGGGAAGGTAGATTA GCAGTCGTTGATGAGGGTGTGGAGAGAAGGGGCCCCTCGTGCACTGTTGGCGGGAAGGTAGATTA A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:402542..402626 26863196 MeRIP-seq:(Medium) rs932975552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55974 RMVar_ID_55974 Human_SNP_ID_218667265 m1A Human chr5 + 402548 402548 402548 GCAGTCGTTGATGAGGGTGTGGAGAGAAGGGGACCCTCGTGCACTGTTGGCGGGAAGGTAGATTA GCAGTCGTTGATGAGGGTGTGGAGAGAAGGGGTCCCTCGTGCACTGTTGGCGGGAAGGTAGATTA A T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:402542..402626 26863196 MeRIP-seq:(Medium) rs932975552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55975 RMVar_ID_55975 Human_SNP_ID_218667407 m1A Human chr5 + 403087 403087 403087 AAGGAAGGAAATGGACACGCACTGTGGCTCGGATCCACCTTGACGACTCTGCGGAGTGAAACAAA AAGGAAGGAAATGGACACGCACTGTGGCTCGGCTCCACCTTGACGACTCTGCGGAGTGAAACAAA A C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:403083..403313 26863196 MeRIP-seq:(Medium) rs1200873223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55976 RMVar_ID_55976 Human_SNP_ID_218667408 m1A Human chr5 + 403087 403087 403087 AAGGAAGGAAATGGACACGCACTGTGGCTCGGATCCACCTTGACGACTCTGCGGAGTGAAACAAA AAGGAAGGAAATGGACACGCACTGTGGCTCGGGTCCACCTTGACGACTCTGCGGAGTGAAACAAA A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:403083..403313 26863196 MeRIP-seq:(Medium) rs1200873223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 55977 RMVar_ID_55977 Human_SNP_ID_218671377 m1A Human chr5 - 417246 417126 417246 TTCTCCAGACTCAGGCCCTGCACATACAGACCAAGCCGCCTTCTCTAGACTCGGGCCCTGCACAT TTCTCCAGACTCAGGCCCTGCACATACAGACC_________________________________ GGGTCTGTATGTGCAGGGCCTGAGTCTGGAGAAGGCCGCTTGGTGTGTATGTGCAGGGCCCATGTCTAGAGAAGGTGGCTTGGTCTGTATGTGCAGGGCCCGAGTCTAGAGAAGGCGGCTT G lnc-SLC9A3-4 RNACentral:URS00009C5F28 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:417235..417391 26863196 MeRIP-seq:(Medium) rs1560917425 Functional Loss DEL dbSNP153 33..65 33 - - - 55978 RMVar_ID_55978 Human_SNP_ID_218671431 m1A Human chr5 - 417246 417246 417246 TTCTCCAGACTCAGGCCCTGCACATACAGACCAAGCCGCCTTCTCTAGACTCGGGCCCTGCACAT TTCTCCAGACTCAGGCCCTGCACATACAGACCGAGCCGCCTTCTCTAGACTCGGGCCCTGCACAT T C lnc-SLC9A3-4 RNACentral:URS00009C5F28 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:417235..417391 26863196 MeRIP-seq:(Medium) rs1049944481 Functional Loss SNV dbSNP153 33..33 33 - - - 55979 RMVar_ID_55979 Human_SNP_ID_218671442 m1A Human chr5 - 417266 417266 417266 CACATATGGACCAAGCCGCCTTCTCCAGACTCAGGCCCTGCACATACAGACCAAGCCGCCTTCTC CACATATGGACCAAGCCGCCTTCTCCAGACTCGGGCCCTGCACATACAGACCAAGCCGCCTTCTC T C lnc-SLC9A3-4 RNACentral:URS00009C5F28 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:417256..417347 26863196 MeRIP-seq:(Medium) rs1408347080 Functional Loss SNV dbSNP153 33..33 33 - - - 55980 RMVar_ID_55980 Human_SNP_ID_218672163 m1A Human chr5 - 420106 420106 420106 GGAACTGCACGGTTCTGCCGCTCTATGGCGGCAGCCTCAGGGCCCGTCAGAGGGAAGCTTAGCTG GGAACTGCACGGTTCTGCCGCTCTATGGCGGCGGCCTCAGGGCCCGTCAGAGGGAAGCTTAGCTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:419998..420175 26863196 MeRIP-seq:(Medium) rs1445466567 Functional Loss SNV dbSNP153 33..33 33 - - - 55981 RMVar_ID_55981 Human_SNP_ID_218672466 m1A Human chr5 + 420854 420854 420854 CAGCCACCCACCCACGCAGCACGCACAGACCCACGCACGCAGCCACCCACCCACGCAGCACGCAC CAGCCACCCACCCACGCAGCACGCACAGACCCGCGCACGCAGCCACCCACCCACGCAGCACGCAC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:420833..420918 26863196 MeRIP-seq:(Medium) rs1285650830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 55982 RMVar_ID_55982 Human_SNP_ID_218672473 m1A Human chr5 + 420866 420863 420867 CACGCAGCACGCACAGACCCACGCACGCAGCCACCCACCCACGCAGCACGCACAGACCCACGCAC CACGCAGCACGCACAGACCCACGCACGCAG____CCACCCACGCAGCACGCACAGACCCACGCAC GCCAC G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr5:420767..420955;chr5:420792..420950 26863196 MeRIP-seq:(Medium) rs773356895 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 55983 RMVar_ID_55983 Human_SNP_ID_218673082 m1A Human chr5 + 422212 422208 422212 CCAGACATGGACCCTGGGTGCCTGTGAGGGTCAGCCTCTGTGTCAGGGCCCAGATTAGCTTCTGA CCAGACATGGACCCTGGGTGCCTGTGAGG____GCCTCTGTGTCAGGGCCCAGATTAGCTTCTGA GGTCA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:422207..422393 26863196 MeRIP-seq:(Medium) rs1355089721 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 55984 RMVar_ID_55984 Human_SNP_ID_218673282 m1A Human chr5 + 422784 422782 422784 TTATGACTACATCCACGTGGACGACCGCCAGGACTTCTGCCGGCAGCTCCACTGGGCCATGGACC TTATGACTACATCCACGTGGACGACCGCCAG__CTTCTGCCGGCAGCTCCACTGGGCCATGGACC GGA G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:422776..422825 26863196 MeRIP-seq:(Medium) rs1264270839 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_631110,Human_Splice_Rec_631111,Human_Splice_Rec_631130,Human_Splice_Rec_631131,Human_Splice_Rec_631148,Human_Splice_Rec_631149,Human_Splice_Rec_631168,Human_Splice_Rec_631178,Human_Splice_Rec_631196,Human_Splice_Rec_631197,Human_Splice_Rec_631207 RMVar_hsa_circ_67941,RMVar_hsa_circ_26604,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 55985 RMVar_ID_55985 Human_SNP_ID_218676989 m1A Human chr5 + 434112 434112 434112 CGCCCATCTCTCACCCGCCGAGCCCGTCCCCCAGTGCCTACTCCAGCCGGACCAGCAGACCCATG CGCCCATCTCTCACCCGCCGAGCCCGTCCCCCGGTGCCTACTCCAGCCGGACCAGCAGACCCATG A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:433862..434175 26863196 MeRIP-seq:(Medium) rs1306456752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27516042 55986 RMVar_ID_55986 Human_SNP_ID_218677026 m1A Human chr5 - 434189 434189 434189 TGAGGGAGCTGGTGCTGCAGGCTCCTCTGGGGAAAGTGGCAGAGGGGAGGGTGCACCTGGTCCTC TGAGGGAGCTGGTGCTGCAGGCTCCTCTGGGGGAAGTGGCAGAGGGGAGGGTGCACCTGGTCCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:434152..434502 32194978 MeRIP-seq:(Medium) rs1356348497 Functional Loss SNV dbSNP153 33..33 33 - - - 55987 RMVar_ID_55987 Human_SNP_ID_218677524 m1A Human chr5 - 435272 435272 435272 GCCTGGGAGGGCTGAGCTAGGTGTGTCACCCGACCGCTTCATCCCCGACTGCGGACTTGGGAGCA GCCTGGGAGGGCTGAGCTAGGTGTGTCACCCGTCCGCTTCATCCCCGACTGCGGACTTGGGAGCA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:435226..435325 26863196 MeRIP-seq:(Medium) rs748524864 Functional Loss SNV dbSNP153 33..33 33 - - - 55988 RMVar_ID_55988 Human_SNP_ID_218677532 m1A Human chr5 + 435283 435282 435283 CCGCAGTCGGGGATGAAGCGGTCGGGTGACACACCTAGCTCAGCCCTCCCAGGCCACCTGCAGCT CCGCAGTCGGGGATGAAGCGGTCGGGTGACAC_CCTAGCTCAGCCCTCCCAGGCCACCTGCAGCT CA C AHRR Ensembl:ENSG00000286169 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:435233..435413 26863196 MeRIP-seq:(Medium) rs1368088202 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_166531,Human_RBP_ID_27516079 55989 RMVar_ID_55989 Human_SNP_ID_218677610 m1A Human chr5 + 435511 435511 435511 CACACTGCCCCACACCGTGCGGCAGGTGCTCCATGGCGCCATGACAGAGTCTGAGGCCAGACCTG CACACTGCCCCACACCGTGCGGCAGGTGCTCCGTGGCGCCATGACAGAGTCTGAGGCCAGACCTG A G AHRR Ensembl:ENSG00000286169 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11740891 Functional Loss SNV dbSNP153 33..33 33 - - - 55990 RMVar_ID_55990 Human_SNP_ID_218677797 m1A Human chr5 + 436175 436175 436175 TCCACTGGGAGTGGCAGGAGCTGTGGGAGCCCATGGGTGAGGGACCCACCACCCCGCTGCACTGT TCCACTGGGAGTGGCAGGAGCTGTGGGAGCCCGTGGGTGAGGGACCCACCACCCCGCTGCACTGT A G AHRR Ensembl:ENSG00000286169 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:436126..436200 26863196 MeRIP-seq:(Medium) rs373101157 Functional Loss SNV dbSNP153 33..33 33 - - - 55991 RMVar_ID_55991 Human_SNP_ID_218677798 m1A Human chr5 + 436175 436175 436176 TCCACTGGGAGTGGCAGGAGCTGTGGGAGCCCATGGGTGAGGGACCCACCACCCCGCTGCACTGT TCCACTGGGAGTGGCAGGAGCTGTGGGAGCCCGCGGGTGAGGGACCCACCACCCCGCTGCACTGT AT GC AHRR Ensembl:ENSG00000286169 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:436126..436200 26863196 MeRIP-seq:(Medium) rs386684256 Functional Loss MNV dbSNP153 33..34 33 - - - 55992 RMVar_ID_55992 Human_SNP_ID_218680173 m1A Human chr5 + 443217 443217 443217 CGGGACCCCGGAGGCGGAGGCAGCGAAGGCGGAGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG CGGGACCCCGGAGGCGGAGGCAGCGAAGGCGGCGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG A C EXOC3 Ensembl:ENSG00000180104 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:443176..443334;chr5:443133..443351;chr5:443126..443258 26863196 MeRIP-seq:(Medium) rs558906544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19015431 Human_Splice_Rec_631213,Human_Splice_Rec_631217,Human_Splice_Rec_631241,Human_Splice_Rec_631263 RMVar_hsa_circ_111883,RMVar_hsa_circ_127694 55993 RMVar_ID_55993 Human_SNP_ID_218680174 m1A Human chr5 + 443217 443217 443217 CGGGACCCCGGAGGCGGAGGCAGCGAAGGCGGAGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG CGGGACCCCGGAGGCGGAGGCAGCGAAGGCGGGGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG A G EXOC3 Ensembl:ENSG00000180104 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:443176..443334;chr5:443133..443351;chr5:443126..443258 26863196 MeRIP-seq:(Medium) rs558906544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19015431 Human_Splice_Rec_631213,Human_Splice_Rec_631217,Human_Splice_Rec_631241,Human_Splice_Rec_631263 RMVar_hsa_circ_111883,RMVar_hsa_circ_127694 55994 RMVar_ID_55994 Human_SNP_ID_218680286 m1A Human chr5 - 443279 443258 443279 CAGGACCTGCCACCGACTCACCCTCTACGGCTACGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG CAGGACCTGCCACCGACTCACCCTCTACGGCT_____________________CCGCCGCCGCCG GCGGCGGCGGCGGCGGCGGCGT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:443147..443339;chr5:443176..443347;chr5:443176..443364;chr5:443176..443350 26863196 MeRIP-seq:(Medium) rs1560933166 Functional Loss DEL dbSNP153 33..53 33 - - - 55995 RMVar_ID_55995 Human_SNP_ID_218680306 m1A Human chr5 - 443279 443273 443279 CAGGACCTGCCACCGACTCACCCTCTACGGCTACGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG CAGGACCTGCCACCGACTCACCCTCTACGGCT______CCGCCGCCGCCGCCGCCGCCGCCGCCG GCGGCGT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:443147..443339;chr5:443176..443347;chr5:443176..443364;chr5:443176..443350 26863196 MeRIP-seq:(Medium) rs1464746229 Functional Loss DEL dbSNP153 33..38 33 - - - 55996 RMVar_ID_55996 Human_SNP_ID_218680313 m1A Human chr5 - 443279 443278 443280 CAGGACCTGCCACCGACTCACCCTCTACGGCTACGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG CAGGACCTGCCACCGACTCACCCTCTACGGC__CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG GTA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:443147..443339;chr5:443176..443347;chr5:443176..443364;chr5:443176..443350 26863196 MeRIP-seq:(Medium) rs1188540135 Functional Loss DEL dbSNP153 32..33 33 - - - 55997 RMVar_ID_55997 Human_SNP_ID_218680325 m1A Human chr5 - 443292 443292 443292 ACCCGCCGGCCGTCAGGACCTGCCACCGACTCACCCTCTACGGCTACGCCGCCGCCGCCGCCGCC ACCCGCCGGCCGTCAGGACCTGCCACCGACTCGCCCTCTACGGCTACGCCGCCGCCGCCGCCGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:443226..443300 26863410 MeRIP-seq:(Medium) rs1412551996 Functional Loss SNV dbSNP153 33..33 33 - - - 55998 RMVar_ID_55998 Human_SNP_ID_218683124 m1A Human chr5 - 453374 453374 453374 TCAATTAGGTCCTGGGTCTCCCTCACAATCTCAGGCACTAGGGAGAAGGCACAAGACACAACATA TCAATTAGGTCCTGGGTCTCCCTCACAATCTCGGGCACTAGGGAGAAGGCACAAGACACAACATA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:453368..453446 26863196 MeRIP-seq:(Medium) rs1444053739 Functional Loss SNV dbSNP153 33..33 33 - - - 55999 RMVar_ID_55999 Human_SNP_ID_218683239 m1A Human chr5 - 453719 453719 453719 AACATTTTCTCCTTCCAATTCTTGGGCCTCCCAGGAGGAACAAAGCCAGTTTGCTTTTTCCGGTC AACATTTTCTCCTTCCAATTCTTGGGCCTCCCGGGAGGAACAAAGCCAGTTTGCTTTTTCCGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:453670..453761 26863196 MeRIP-seq:(Medium) rs549225307 Functional Loss SNV dbSNP153 33..33 33 - - - 56000 RMVar_ID_56000 Human_SNP_ID_218683240 m1A Human chr5 - 453719 453719 453719 AACATTTTCTCCTTCCAATTCTTGGGCCTCCCAGGAGGAACAAAGCCAGTTTGCTTTTTCCGGTC AACATTTTCTCCTTCCAATTCTTGGGCCTCCCCGGAGGAACAAAGCCAGTTTGCTTTTTCCGGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:453670..453761 26863196 MeRIP-seq:(Medium) rs549225307 Functional Loss SNV dbSNP153 33..33 33 - - - 56001 RMVar_ID_56001 Human_SNP_ID_218683319 m1A Human chr5 - 453946 453946 453946 CCTGCATCCGCGTGCTCAGGGCTTGGTGGTACATGTTCAGGAGGTTCTTAAAGATCTCATAGTGG CCTGCATCCGCGTGCTCAGGGCTTGGTGGTACGTGTTCAGGAGGTTCTTAAAGATCTCATAGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:453896..453964 26863196 MeRIP-seq:(Medium) rs753925491 Functional Loss SNV dbSNP153 33..33 33 - - - 56002 RMVar_ID_56002 Human_SNP_ID_218683320 m1A Human chr5 - 453946 453946 453946 CCTGCATCCGCGTGCTCAGGGCTTGGTGGTACATGTTCAGGAGGTTCTTAAAGATCTCATAGTGG CCTGCATCCGCGTGCTCAGGGCTTGGTGGTACCTGTTCAGGAGGTTCTTAAAGATCTCATAGTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:453896..453964 26863196 MeRIP-seq:(Medium) rs753925491 Functional Loss SNV dbSNP153 33..33 33 - - - 56003 RMVar_ID_56003 Human_SNP_ID_218686622 m1A Human chr5 + 465196 465196 465196 CATGCAGAAGCGCATTTCCTTCCGGAGCCCGGAGGAGCGCAAGGAGGGTGCCGAGAAGATGGTTA CATGCAGAAGCGCATTTCCTTCCGGAGCCCGGGGGAGCGCAAGGAGGGTGCCGAGAAGATGGTTA A G EXOC3 Ensembl:ENSG00000180104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:465108..465291;chr5:465101..465225 26863196 MeRIP-seq:(Medium) rs779952402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250421 Human_Splice_Rec_631236,Human_Splice_Rec_631237,Human_Splice_Rec_631253,Human_Splice_Rec_631286,Human_Splice_Rec_631287,Human_Splice_Rec_631303,Human_Splice_Rec_631319 RMVar_hsa_circ_2325,RMVar_hsa_circ_111883,RMVar_hsa_circ_229953,RMVar_hsa_circ_368081,RMVar_hsa_circ_229958,RMVar_hsa_circ_93932,RMVar_hsa_circ_21943,RMVar_hsa_circ_16684,RMVar_hsa_circ_355784,RMVar_hsa_circ_378243,RMVar_hsa_circ_268403 56004 RMVar_ID_56004 Human_SNP_ID_218686953 m1A Human chr5 - 466082 466082 466082 TGTCACAGCCCCGCCCCCACCCCACTGTCCCCACCCGGGATGTGCCCCTCGAGCTCCACCCACCC TGTCACAGCCCCGCCCCCACCCCACTGTCCCCCCCCGGGATGTGCCCCTCGAGCTCCACCCACCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:466077..466925 32194978 MeRIP-seq:(Medium) rs1217759283 Functional Loss SNV dbSNP153 33..33 33 - - - 56005 RMVar_ID_56005 Human_SNP_ID_218687236 m1A Human chr5 - 466916 466916 466916 AAGGCAGGGACCGAGGCTGTGGAGGGGCGAGCAGGGCAGGCCGGCGGAGGCTACTTGAGCAGCTT AAGGCAGGGACCGAGGCTGTGGAGGGGCGAGCGGGGCAGGCCGGCGGAGGCTACTTGAGCAGCTT T C AC010442.1 Ensembl:ENSG00000188242 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:466720..467031 26863196 MeRIP-seq:(Medium) rs1438723701 Functional Loss SNV dbSNP153 33..33 33 - - - 56006 RMVar_ID_56006 Human_SNP_ID_218688967 m1A Human chr5 + 472510 472510 472510 GGGCACCCCGGGCGACCTCCGCGCCAGGTGCGACAGCTCAGGCCGGAGACCTCGTCTGTGGGGAC GGGCACCCCGGGCGACCTCCGCGCCAGGTGCGGCAGCTCAGGCCGGAGACCTCGTCTGTGGGGAC A G lnc-EXOC3-3,lnc-EXOC3-3:2,lnc-EXOC3-3:3 RNACentral:URS00008B789D,RNACentral:URS00008B4563,RNACentral:URS00008B5296 lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:472460..472609 26863196 MeRIP-seq:(Medium) rs535439210 Functional Loss SNV dbSNP153 33..33 33 - - - 56007 RMVar_ID_56007 Human_SNP_ID_218689167 m1A Human chr5 + 472873 472873 472873 GGGGCCCGGAACCTTGGGCTGGTTTCACGCAAATCCGTTTGGGGCGAGCCTCGGTTTCCCGGCAG GGGGCCCGGAACCTTGGGCTGGTTTCACGCAAGTCCGTTTGGGGCGAGCCTCGGTTTCCCGGCAG A G lnc-EXOC3-3,lnc-EXOC3-3:2 RNACentral:URS00008B789D,RNACentral:URS00008B5296 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:472825..473050 26863196 MeRIP-seq:(Medium) rs1357295018 Functional Loss SNV dbSNP153 33..33 33 - - - 56008 RMVar_ID_56008 Human_SNP_ID_218689199 m1A Human chr5 + 472968 472957 472968 GGCGCGCGGACCCTTCCCGCCGGCGGCGTCACAGCGGCGTCTCCTCCTGCTCCAGCGCGTGCGGC GGCGCGCGGACCCTTCCCGCCG___________GCGGCGTCTCCTCCTGCTCCAGCGCGTGCGGC GGCGGCGTCACA G lnc-EXOC3-3,lnc-EXOC3-3:2 RNACentral:URS00008B789D,RNACentral:URS00008B5296 lincRNA,lincRNA exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:472867..473053 26863410 MeRIP-seq:(Medium) rs1427574275 Functional Loss DEL dbSNP153 23..33 33 - - - 56009 RMVar_ID_56009 Human_SNP_ID_218689511 m1A Human chr5 + 473538 473538 473538 AGGCTCGGCGTCCGCTGGGGCCTCCTCCCAGGACCCGGGTTCGCGGGGCAGAGGCGGAAGCAGCA AGGCTCGGCGTCCGCTGGGGCCTCCTCCCAGGTCCCGGGTTCGCGGGGCAGAGGCGGAAGCAGCA A T SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:473376..474125 32194978 MeRIP-seq:(Medium) rs964267162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783058,Human_RBP_ID_5614540 56010 RMVar_ID_56010 Human_SNP_ID_218689910 m1A Human chr5 + 474693 474693 474693 GGAGAGGAGCTGCGGAGAGGGGTTAGGCGGGGAGAGAGAGAGCGAGCCAGGTTCAGGTCCAGGGA GGAGAGGAGCTGCGGAGAGGGGTTAGGCGGGGGGAGAGAGAGCGAGCCAGGTTCAGGTCCAGGGA A G SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:474576..474800 26863196 MeRIP-seq:(Medium) rs1170192389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212979,Human_RBP_ID_8269279,Human_RBP_ID_17069778,Human_RBP_ID_24107547,Human_RBP_ID_26791991 56011 RMVar_ID_56011 Human_SNP_ID_218689913 m1A Human chr5 + 474705 474694 474705 CGGAGAGGGGTTAGGCGGGGAGAGAGAGAGCGAGCCAGGTTCAGGTCCAGGGAGGAGAGAGACAG CGGAGAGGGGTTAGGCGGGGAG___________GCCAGGTTCAGGTCCAGGGAGGAGAGAGACAG GAGAGAGAGCGA G SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:473226..476932;chr5:473270..475547;chr5:473272..476097;chr5:473260..476214 26863196 MeRIP-seq:(Medium) rs1560947112 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_8212979,Human_RBP_ID_8269279,Human_RBP_ID_17069778,Human_RBP_ID_24107547,Human_RBP_ID_26791991 56012 RMVar_ID_56012 Human_SNP_ID_218689914 m1A Human chr5 + 474695 474695 474695 AGAGGAGCTGCGGAGAGGGGTTAGGCGGGGAGAGAGAGAGCGAGCCAGGTTCAGGTCCAGGGAGG AGAGGAGCTGCGGAGAGGGGTTAGGCGGGGAGGGAGAGAGCGAGCCAGGTTCAGGTCCAGGGAGG A G SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:474381..474751 26863196 MeRIP-seq:(Medium) rs1412654378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212979,Human_RBP_ID_8269279,Human_RBP_ID_17069778,Human_RBP_ID_24107547,Human_RBP_ID_26791991 56013 RMVar_ID_56013 Human_SNP_ID_218690225 m1A Human chr5 - 475289 475289 475289 ACCTGTGCTGCCTGTGGCGTGTGGGGTCATGGATGTGGGGGAAGGGCCCGCAACCTGAAAGGCAC ACCTGTGCTGCCTGTGGCGTGTGGGGTCATGGGTGTGGGGGAAGGGCCCGCAACCTGAAAGGCAC T C SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:474964..475555 32194978 MeRIP-seq:(Medium) rs1439334394 Functional Loss SNV dbSNP153 33..33 33 - - - 56014 RMVar_ID_56014 Human_SNP_ID_218691111 m1A Human chr5 - 477315 477315 477315 CTGTCTCCTACCTCCTGTATGTGGCCATGGTCATGCAGCTTCCCTGGGGAAGAGCCCAGCCTCGG CTGTCTCCTACCTCCTGTATGTGGCCATGGTCTTGCAGCTTCCCTGGGGAAGAGCCCAGCCTCGG T A SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:477093..477464 26863196 MeRIP-seq:(Medium) rs369798965 Functional Loss SNV dbSNP153 33..33 33 - - - 56015 RMVar_ID_56015 Human_SNP_ID_218691112 m1A Human chr5 - 477315 477315 477315 CTGTCTCCTACCTCCTGTATGTGGCCATGGTCATGCAGCTTCCCTGGGGAAGAGCCCAGCCTCGG CTGTCTCCTACCTCCTGTATGTGGCCATGGTCGTGCAGCTTCCCTGGGGAAGAGCCCAGCCTCGG T C SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:477093..477464 26863196 MeRIP-seq:(Medium) rs369798965 Functional Loss SNV dbSNP153 33..33 33 - - - 56016 RMVar_ID_56016 Human_SNP_ID_218691333 m1A Human chr5 - 477832 477832 477832 TGCTCCGTTCTCTACCTGATTCAGTTCTGGACATGAGGCCAATGGAGTTTTAGGGTCTCCTGCAG TGCTCCGTTCTCTACCTGATTCAGTTCTGGACGTGAGGCCAATGGAGTTTTAGGGTCTCCTGCAG T C SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:477791..478096 26863196 MeRIP-seq:(Medium) rs898089166 Functional Loss SNV dbSNP153 33..33 33 - - - 56017 RMVar_ID_56017 Human_SNP_ID_218691334 m1A Human chr5 - 477832 477832 477832 TGCTCCGTTCTCTACCTGATTCAGTTCTGGACATGAGGCCAATGGAGTTTTAGGGTCTCCTGCAG TGCTCCGTTCTCTACCTGATTCAGTTCTGGACCTGAGGCCAATGGAGTTTTAGGGTCTCCTGCAG T G SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:477791..478096 26863196 MeRIP-seq:(Medium) rs898089166 Functional Loss SNV dbSNP153 33..33 33 - - - 56018 RMVar_ID_56018 Human_SNP_ID_218691583 m1A Human chr5 + 478507 478507 478507 AAAGCAGCCGCCCTGGGTGAGAGCCAGGAGGGACACTGGGCAGGCAGATGCCACCCCAGGTGTGG AAAGCAGCCGCCCTGGGTGAGAGCCAGGAGGGTCACTGGGCAGGCAGATGCCACCCCAGGTGTGG A T SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:478499..478577 26863196 MeRIP-seq:(Medium) rs958559087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5614555,Human_RBP_ID_8215003 56019 RMVar_ID_56019 Human_SNP_ID_218692337 m1A Human chr5 - 480694 480694 480694 AAGCTCAGCTGCGGTTCTCCGTGGCCACAGTGACTCTGCTCCGGGTACCCAGTCCCCGACTCCTT AAGCTCAGCTGCGGTTCTCCGTGGCCACAGTGCCTCTGCTCCGGGTACCCAGTCCCCGACTCCTT T G SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:480653..480758 26863196 MeRIP-seq:(Medium) rs1210937804 Functional Loss SNV dbSNP153 33..33 33 - - - 56020 RMVar_ID_56020 Human_SNP_ID_218692338 m1A Human chr5 - 480700 480700 480700 TTCATAAAGCTCAGCTGCGGTTCTCCGTGGCCACAGTGACTCTGCTCCGGGTACCCAGTCCCCGA TTCATAAAGCTCAGCTGCGGTTCTCCGTGGCCCCAGTGACTCTGCTCCGGGTACCCAGTCCCCGA T G SLC9A3 Ensembl:ENSG00000066230 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:480673..480760 26863196 MeRIP-seq:(Medium) rs1050135052 Functional Loss SNV dbSNP153 33..33 33 - - - 56021 RMVar_ID_56021 Human_SNP_ID_218692383 m1A Human chr5 + 480833 480830 480833 AGGGCAAATTGTATGTGCTCCTTACTGGGTTTATTATAAGTGTCACATGTTTTTTATAATAAAAC AGGGCAAATTGTATGTGCTCCTTACTGGGT___TTATAAGTGTCACATGTTTTTTATAATAAAAC TTTA T SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1470767405 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_643015,Human_RBP_ID_1655114 56022 RMVar_ID_56022 Human_SNP_ID_218692385 m1A Human chr5 + 480833 480833 480833 AGGGCAAATTGTATGTGCTCCTTACTGGGTTTATTATAAGTGTCACATGTTTTTTATAATAAAAC AGGGCAAATTGTATGTGCTCCTTACTGGGTTTGTTATAAGTGTCACATGTTTTTTATAATAAAAC A G SLC9A3-AS1 Ensembl:ENSG00000225138 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1043356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_643015,Human_RBP_ID_1655114 GWAS_ID_6663 56023 RMVar_ID_56023 Human_SNP_ID_218730854 m1A Human chr5 - 610751 610751 610751 GTGCAGGAGGTGTGTGTAGATGTGTGTGCAGGAGGTATACACAGGGTTTGTGCAGAGGATGTGTG GTGCAGGAGGTGTGTGTAGATGTGTGTGCAGGGGGTATACACAGGGTTTGTGCAGAGGATGTGTG T C AC106772.1 Ensembl:ENSG00000249650 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:610701..610792 26863196 MeRIP-seq:(Medium) rs1333398693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24110950,Human_RBP_ID_27741977 56024 RMVar_ID_56024 Human_SNP_ID_218730907 m1A Human chr5 + 610891 610889 610891 CCCCCACACATAGCCCCTACACACACCTCTGCACATACTGTTGCACACACCCCCACACATAGCTC CCCCCACACATAGCCCCTACACACACCTCTG__CATACTGTTGCACACACCCCCACACATAGCTC GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:610861..611027 26863196 MeRIP-seq:(Medium) rs765755757 Functional Loss DEL dbSNP153 32..33 33 - - - 56025 RMVar_ID_56025 Human_SNP_ID_218730908 m1A Human chr5 + 610891 610891 610891 CCCCCACACATAGCCCCTACACACACCTCTGCACATACTGTTGCACACACCCCCACACATAGCTC CCCCCACACATAGCCCCTACACACACCTCTGCTCATACTGTTGCACACACCCCCACACATAGCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:610861..611027 26863196 MeRIP-seq:(Medium) rs1466515123 Functional Loss SNV dbSNP153 33..33 33 - - - 56026 RMVar_ID_56026 Human_SNP_ID_218730911 m1A Human chr5 - 610897 610897 610897 GTGCAGGAGCTATGTGTGGGGGTGTGTGCAACAGTATGTGCAGAGGTGTGTGTAGGGGCTATGTG GTGCAGGAGCTATGTGTGGGGGTGTGTGCAACGGTATGTGCAGAGGTGTGTGTAGGGGCTATGTG T C AC106772.1 Ensembl:ENSG00000249650 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:610851..610992 26863196 MeRIP-seq:(Medium) rs1192167804 Functional Loss SNV dbSNP153 33..33 33 - - - 56027 RMVar_ID_56027 Human_SNP_ID_218731425 m1A Human chr5 - 612441 612441 612441 GCTTGCACCCCCGCCCGCCCTCCGGCGCACCCAGGTCGCGGTGAGGCCCTAAGCCGCTCTTCGCC GCTTGCACCCCCGCCCGCCCTCCGGCGCACCCGGGTCGCGGTGAGGCCCTAAGCCGCTCTTCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:612392..612805 26863196 MeRIP-seq:(Medium) rs1161899627 Functional Loss SNV dbSNP153 33..33 33 - - - 56028 RMVar_ID_56028 Human_SNP_ID_218731426 m1A Human chr5 - 612441 612441 612441 GCTTGCACCCCCGCCCGCCCTCCGGCGCACCCAGGTCGCGGTGAGGCCCTAAGCCGCTCTTCGCC GCTTGCACCCCCGCCCGCCCTCCGGCGCACCCCGGTCGCGGTGAGGCCCTAAGCCGCTCTTCGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:612392..612805 26863196 MeRIP-seq:(Medium) rs1161899627 Functional Loss SNV dbSNP153 33..33 33 - - - 56029 RMVar_ID_56029 Human_SNP_ID_218731529 m1A Human chr5 + 612687 612687 612687 CGGCGTCCCGGCCCCTGCCTGTCTATCGGGTCACTGGTTCCGTGACTGGGGGTTACATCCGCTGA CGGCGTCCCGGCCCCTGCCTGTCTATCGGGTCGCTGGTTCCGTGACTGGGGGTTACATCCGCTGA A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:612652..612813 26863196 MeRIP-seq:(Medium) rs1338305797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2941496,Human_RBP_ID_5151056,Human_RBP_ID_8619228,Human_RBP_ID_15479337,Human_RBP_ID_18502033,Human_RBP_ID_24433403,Human_RBP_ID_26791722 RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 56030 RMVar_ID_56030 Human_SNP_ID_218732546 m1A Human chr5 - 616751 616751 616751 TGGCCTTGCGCAGCAGCCAGCACCGGGGTGTGAGAATGGATCCTGACTGCTGTCCCGGCCTGGCT TGGCCTTGCGCAGCAGCCAGCACCGGGGTGTGGGAATGGATCCTGACTGCTGTCCCGGCCTGGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:616728..616851 32194978 MeRIP-seq:(Medium) rs1401803099 Functional Loss SNV dbSNP153 33..33 33 - - - 56031 RMVar_ID_56031 Human_SNP_ID_218732579 m1A Human chr5 - 616799 616799 616799 ACACACACACACACATACACACACACACACACACACCCCTCGTCCACCTGGCCTTGCGCAGCAGC ACACACACACACACATACACACACACACACACCCACCCCTCGTCCACCTGGCCTTGCGCAGCAGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:616768..616993 26863196 MeRIP-seq:(Medium) rs1378412964 Functional Loss SNV dbSNP153 33..33 33 - - - 56032 RMVar_ID_56032 Human_SNP_ID_218732968 m1A Human chr5 + 618084 618084 618084 AGCAGACAGGTTACCCGACGAGTGGGTTTCAGATGGTGATGGCTGCAAGGGGTGACAGAATTGAG AGCAGACAGGTTACCCGACGAGTGGGTTTCAGGTGGTGATGGCTGCAAGGGGTGACAGAATTGAG A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:618046..618217 26863196 MeRIP-seq:(Medium) rs1011484146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15482052,Human_RBP_ID_18501612,Human_RBP_ID_24111382 RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 56033 RMVar_ID_56033 Human_SNP_ID_218733638 m1A Human chr5 - 620175 620175 620175 CAACCTTCACCACGGGGTTCAGCCGGAAGTCCACATCCACGAGCTCGGTTAAGGCGTGGAGCCGA CAACCTTCACCACGGGGTTCAGCCGGAAGTCCTCATCCACGAGCTCGGTTAAGGCGTGGAGCCGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:620124..620225 26863196 MeRIP-seq:(Medium) rs754391753 Functional Loss SNV dbSNP153 33..33 33 - - - 56034 RMVar_ID_56034 Human_SNP_ID_218739106 m1A Human chr5 + 637703 637703 637703 CCCGGAGAGAACTCATGGGTCCTCCGTGCCCAAGGAGAGCCTGAGCAGACAGGACAGCTCAGAAA CCCGGAGAGAACTCATGGGTCCTCCGTGCCCAGGGAGAGCCTGAGCAGACAGGACAGCTCAGAAA A G CEP72 Ensembl:ENSG00000112877 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:637654..637849 26863196 MeRIP-seq:(Medium) rs1416485152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5531824 RMVar_hsa_circ_31508,RMVar_hsa_circ_296269,RMVar_hsa_circ_310402,RMVar_hsa_circ_108129,RMVar_hsa_circ_51644,RMVar_hsa_circ_60684,RMVar_hsa_circ_229964,RMVar_hsa_circ_229965,RMVar_hsa_circ_127958,RMVar_hsa_circ_340429,RMVar_hsa_circ_229971,RMVar_hsa_circ_229973,RMVar_hsa_circ_330905,RMVar_hsa_circ_229974,RMVar_hsa_circ_107416 56035 RMVar_ID_56035 Human_SNP_ID_218740458 m1A Human chr5 + 641581 641581 641581 GCAGCCTCTGTTTAAACGCACGTGGCCCCCCCACCCCGCCTGGAAGCCTCTGCACGTGGCCTTCA GCAGCCTCTGTTTAAACGCACGTGGCCCCCCCCCCCCGCCTGGAAGCCTCTGCACGTGGCCTTCA A C CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:641545..641775 26863196 MeRIP-seq:(Medium) rs1257972552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5326715,Human_RBP_ID_5531836,Human_RBP_ID_22099283 RMVar_hsa_circ_296269,RMVar_hsa_circ_310402,RMVar_hsa_circ_108129,RMVar_hsa_circ_60684,RMVar_hsa_circ_229964,RMVar_hsa_circ_229965,RMVar_hsa_circ_127958,RMVar_hsa_circ_340429,RMVar_hsa_circ_229971,RMVar_hsa_circ_229973,RMVar_hsa_circ_330905,RMVar_hsa_circ_229974,RMVar_hsa_circ_107416 56036 RMVar_ID_56036 Human_SNP_ID_218740651 m1A Human chr5 - 642059 642059 642059 CTGGACGGGGGACCACGTGTGCTTAAATGCAGAGGCTTCTAGACGGGGGACCACGTGTGTTTAAA CTGGACGGGGGACCACGTGTGCTTAAATGCAGTGGCTTCTAGACGGGGGACCACGTGTGTTTAAA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:642001..642075 26863196 MeRIP-seq:(Medium) rs1038609369 Functional Loss SNV dbSNP153 33..33 33 - - - 56037 RMVar_ID_56037 Human_SNP_ID_218742539 m1A Human chr5 + 648179 648166 648179 TGACCCATGAGGTGTGGATGTGAGGTCTGACCATGAGGTGTGACCACGAGGCATGGACTGTGAGA TGACCCATGAGGTGTGGATG_____________TGAGGTGTGACCACGAGGCATGGACTGTGAGA GTGAGGTCTGACCA G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:648135..648224 26863196 MeRIP-seq:(Medium) rs1431991924 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_5242196,Human_RBP_ID_5655492,Human_RBP_ID_8213360,Human_RBP_ID_9335122,Human_RBP_ID_24112133,Human_RBP_ID_24385517 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 56038 RMVar_ID_56038 Human_SNP_ID_218742683 m1A Human chr5 + 648483 648470 648483 TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTATGACTGTGAGGTGTGACTGTGAGGTGTGGACT TGAGGTGTGACTGTGAGGTG_____________TGACTGTGAGGTGTGACTGTGAGGTGTGGACT GTGACTGTGAGGTA G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:648441..648545;chr5:648426..648558 26863196 MeRIP-seq:(Medium) rs1382470872 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_5655494,Human_RBP_ID_24124148 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 56039 RMVar_ID_56039 Human_SNP_ID_218742693 m1A Human chr5 + 648483 648483 648483 TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTATGACTGTGAGGTGTGACTGTGAGGTGTGGACT TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGGACT A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:648441..648545;chr5:648426..648558 26863196 MeRIP-seq:(Medium) rs62639482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5655494,Human_RBP_ID_24124148 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 56040 RMVar_ID_56040 Human_SNP_ID_218742940 m1A Human chr5 - 648911 648845 648911 ACAGTCACACCTCACAGTCACACCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCACACCT ACAGTCACACCTCACAGTCACACCTCACAGTC_________________________________ GGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGCGTGGACTGTGAGGGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:648867..648957;chr5:648849..648973;chr5:648853..648966 26863196 MeRIP-seq:(Medium) rs1561062002 Functional Loss DEL dbSNP153 33..65 33 - - - 56041 RMVar_ID_56041 Human_SNP_ID_218742968 m1A Human chr5 - 648911 648885 648911 ACAGTCACACCTCACAGTCACACCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCACACCT ACAGTCACACCTCACAGTCACACCTCACAGTC__________________________CACACCT GACTGTGAGGCGTGGACTGTGAGGGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:648867..648957;chr5:648849..648973;chr5:648853..648966 26863196 MeRIP-seq:(Medium) rs1561062095 Functional Loss DEL dbSNP153 33..58 33 - - - 56042 RMVar_ID_56042 Human_SNP_ID_218742977 m1A Human chr5 - 648911 648898 648911 ACAGTCACACCTCACAGTCACACCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCACACCT ACAGTCACACCTCACAGTCACACCTCACAGTC_____________CACGCCTCACAGTCACACCT GGACTGTGAGGGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:648867..648957;chr5:648849..648973;chr5:648853..648966 26863196 MeRIP-seq:(Medium) rs1375612069 Functional Loss DEL dbSNP153 33..45 33 - - - 56043 RMVar_ID_56043 Human_SNP_ID_218742990 m1A Human chr5 - 648911 648911 648911 ACAGTCACACCTCACAGTCACACCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCACACCT ACAGTCACACCTCACAGTCACACCTCACAGTCCCCCCTCACAGTCCACGCCTCACAGTCACACCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:648867..648957;chr5:648849..648973;chr5:648853..648966 26863196 MeRIP-seq:(Medium) rs1450511955 Functional Loss SNV dbSNP153 33..33 33 - - - 56044 RMVar_ID_56044 Human_SNP_ID_218743129 m1A Human chr5 + 649140 649140 649140 ACTGTGAGGTGTGAATGTGAGGCGTGACTGTGAGGCGTGACTGTGAGGCGTGACTGTGAGGTGTG ACTGTGAGGTGTGAATGTGAGGCGTGACTGTGTGGCGTGACTGTGAGGCGTGACTGTGAGGTGTG A T CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:649104..649195 26863196 MeRIP-seq:(Medium) rs1379640894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5151059,Human_RBP_ID_5242199,Human_RBP_ID_5302205,Human_RBP_ID_5655499,Human_RBP_ID_8212988,Human_RBP_ID_9335124,Human_RBP_ID_21186108,Human_RBP_ID_24124149,Human_RBP_ID_24385520 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 56045 RMVar_ID_56045 Human_SNP_ID_218743231 m1A Human chr5 - 649316 649306 649316 CAGTCCACGCCTCACAGTCACGCCTCACAGTCACGCCTCAGTCACGCCTCACAGTCCATGCCTCA CAGTCCACGCCTCACAGTCACGCCTCACAGTC__________CACGCCTCACAGTCCATGCCTCA GACTGAGGCGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:649265..649458;chr5:649250..649476;chr5:649061..649479;chr5:649073..649476 26863196 MeRIP-seq:(Medium) rs1275051903 Functional Loss DEL dbSNP153 33..42 33 - - - 56046 RMVar_ID_56046 Human_SNP_ID_218743580 m1A Human chr5 - 649898 649898 649898 CAGTCCACACCTCACAGTCACACCTCAGTCACACCTCACAGTCCCACCTCACAGTCCACACCTCA CAGTCCACACCTCACAGTCACACCTCAGTCACGCCTCACAGTCCCACCTCACAGTCCACACCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:649873..649967;chr5:649827..649993;chr5:649820..650002 26863196 MeRIP-seq:(Medium) rs1319293543 Functional Loss SNV dbSNP153 33..33 33 - - - 56047 RMVar_ID_56047 Human_SNP_ID_218743722 m1A Human chr5 + 650179 650171 650180 AGGCGTGGACTGTGAGGTGTGACTGAGGTGTGACTGAGGTGTGACTGTGAGGCGTGGACTGTGAG AGGCGTGGACTGTGAGGTGTGACTG_________TGAGGTGTGACTGTGAGGCGTGGACTGTGAG GAGGTGTGAC G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:650145..650224;chr5:650050..650243 26863196 MeRIP-seq:(Medium) rs1261467866 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_5242203,Human_RBP_ID_5302472,Human_RBP_ID_5655504,Human_RBP_ID_7458972,Human_RBP_ID_9335128,Human_RBP_ID_24112564,Human_RBP_ID_24385523 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 56048 RMVar_ID_56048 Human_SNP_ID_218743936 m1A Human chr5 - 650747 650706 650747 CAGTCACACCTCACAGTCCACGCCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCCACGCC CAGTCACACCTCACAGTCCACGCCTCACAGTC_________________________________ GGACTGTGAGGCGTGGACTGTGAGGCGTGGACTGTGAGGGGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:650692..650802 26863196 MeRIP-seq:(Medium) rs1375846914 Functional Loss DEL dbSNP153 33..65 33 - - - 56049 RMVar_ID_56049 Human_SNP_ID_218743952 m1A Human chr5 - 650747 650747 650747 CAGTCACACCTCACAGTCCACGCCTCACAGTCACCCCTCACAGTCCACGCCTCACAGTCCACGCC CAGTCACACCTCACAGTCCACGCCTCACAGTCCCCCCTCACAGTCCACGCCTCACAGTCCACGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:650692..650802 26863196 MeRIP-seq:(Medium) rs1330104357 Functional Loss SNV dbSNP153 33..33 33 - - - 56050 RMVar_ID_56050 Human_SNP_ID_218744272 m1A Human chr5 - 651374 651374 651374 TCCACAACTCTCAGTCCACACCTCACATTCACAACTCACAGTCCATGCCTCAGTCACACCTCACA TCCACAACTCTCAGTCCACACCTCACATTCACGACTCACAGTCCATGCCTCAGTCACACCTCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:651310..651803 26863196 MeRIP-seq:(Medium) rs1478275345 Functional Loss SNV dbSNP153 33..33 33 - - - 56051 RMVar_ID_56051 Human_SNP_ID_218747113 m1A Human chr5 + 661221 661220 661222 ACCTATTCCTGTGTCCTGGTGTCACCCCCAACAGAACCTGTCCCTCTCTCCTGGTGTCACCCCTG ACCTATTCCTGTGTCCTGGTGTCACCCCCAAC__AACCTGTCCCTCTCTCCTGGTGTCACCCCTG CAG C CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:661218..661322 26863196 MeRIP-seq:(Medium) rs1275968125 Functional Loss DEL dbSNP153 33..34 33 - - - 56052 RMVar_ID_56052 Human_SNP_ID_218747151 m1A Human chr5 - 661305 661305 661305 GGGACAGGTTCTGTTGGGGGTGACAAGAGGAGACAGGGACAGGTTCTGTCGGGGGTGACACCAGG GGGACAGGTTCTGTTGGGGGTGACAAGAGGAGGCAGGGACAGGTTCTGTCGGGGGTGACACCAGG T C TPPP Ensembl:ENSG00000171368 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:661254..661358 26863196 MeRIP-seq:(Medium) rs1347705503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56053 RMVar_ID_56053 Human_SNP_ID_218748751 m1A Human chr5 + 665621 665613 665622 GCCCCACCCTCCAGGCTATGCCCCCCCAATCCATGCCCCTTCAGACCAAGCCTCCCCAGGACCCC GCCCCACCCTCCAGGCTATGCCCCC_________GCCCCTTCAGACCAAGCCTCCCCAGGACCCC CCCAATCCAT C CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:665574..665639 26863196 MeRIP-seq:(Medium) rs1561079883 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_17090413 56054 RMVar_ID_56054 Human_SNP_ID_218748761 m1A Human chr5 + 665621 665621 665621 GCCCCACCCTCCAGGCTATGCCCCCCCAATCCATGCCCCTTCAGACCAAGCCTCCCCAGGACCCC GCCCCACCCTCCAGGCTATGCCCCCCCAATCCCTGCCCCTTCAGACCAAGCCTCCCCAGGACCCC A C CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:665574..665639 26863196 MeRIP-seq:(Medium) rs1457797022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17090413 56055 RMVar_ID_56055 Human_SNP_ID_218748826 m1A Human chr5 - 665858 665818 665858 GGTGGTCAGGAGGGACATGGATTGGGGGCGTGACCTGGGGGGGGTCCTGGGAGGCGTGGTCAGGA GGTGGTCAGGAGGGACATGGATTGGGGGCGTG_________________________________ CCACGCCCTCCTGACCACGCCTCCCAGGACCCCCCCCAGGT C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:665744..665871 26863196 MeRIP-seq:(Medium) rs1197285186 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56056 RMVar_ID_56056 Human_SNP_ID_218748844 m1A Human chr5 - 665858 665858 665858 GGTGGTCAGGAGGGACATGGATTGGGGGCGTGACCTGGGGGGGGTCCTGGGAGGCGTGGTCAGGA GGTGGTCAGGAGGGACATGGATTGGGGGCGTGGCCTGGGGGGGGTCCTGGGAGGCGTGGTCAGGA T C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:665744..665871 26863196 MeRIP-seq:(Medium) rs1403779130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56057 RMVar_ID_56057 Human_SNP_ID_218748845 m1A Human chr5 - 665858 665858 665858 GGTGGTCAGGAGGGACATGGATTGGGGGCGTGACCTGGGGGGGGTCCTGGGAGGCGTGGTCAGGA GGTGGTCAGGAGGGACATGGATTGGGGGCGTGCCCTGGGGGGGGTCCTGGGAGGCGTGGTCAGGA T G TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:665744..665871 26863196 MeRIP-seq:(Medium) rs1403779130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56058 RMVar_ID_56058 Human_SNP_ID_218749821 m1A Human chr5 - 668385 668288 668385 CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGAGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT CTCTCTGTGTGCTTGTCGGTACTTCCCTGACG_________________________________ CCGTCAGGGAAGTACCGACAAGCACACAGAGAGGGGGCCGTGTGGGCGCCGTCAGGGAAGTGCGGACAAGCACACTGGAGAGGGGTCCGCGTGGGCCT C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:668336..668457;chr5:668334..668423 26863196 MeRIP-seq:(Medium) rs1561082071 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56059 RMVar_ID_56059 Human_SNP_ID_218749879 m1A Human chr5 - 668385 668383 668385 CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGAGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT CTCTCTGTGTGCTTGTCGGTACTTCCCTGACG__GCCCACGCGGACCCCTCTCCAGTGTGCTTGT CCT C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:668336..668457;chr5:668334..668423 26863196 MeRIP-seq:(Medium) rs1379881091 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56060 RMVar_ID_56060 Human_SNP_ID_218749882 m1A Human chr5 - 668385 668385 668385 CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGAGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGGGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT T C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:668336..668457;chr5:668334..668423 26863196 MeRIP-seq:(Medium) rs11738955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56061 RMVar_ID_56061 Human_SNP_ID_218749883 m1A Human chr5 - 668385 668385 668385 CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGAGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGCGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT T G TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:668336..668457;chr5:668334..668423 26863196 MeRIP-seq:(Medium) rs11738955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56062 RMVar_ID_56062 Human_SNP_ID_218751919 m1A Human chr5 - 673491 673491 673491 GGTGGCCAGGACTGGGACTCCGGCCTGAGGGGAGGCCAAGGGATTCTGACCTCCCCCCCTCCCCA GGTGGCCAGGACTGGGACTCCGGCCTGAGGGGGGGCCAAGGGATTCTGACCTCCCCCCCTCCCCA T C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:673441..673688 26863196 MeRIP-seq:(Medium) rs935707176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56063 RMVar_ID_56063 Human_SNP_ID_218752732 m1A Human chr5 - 675329 675322 675330 ACACCCCCACACTGCACCCCCAGCCACACTGCACCCCCGGCCACACTGTACCTCCCACGCTGCAC ACACCCCCACACTGCACCCCCAGCCACACTG________GCCACACTGTACCTCCCACGCTGCAC CCGGGGGTG C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:675097..675704 26863196 MeRIP-seq:(Medium) rs1279083944 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56064 RMVar_ID_56064 Human_SNP_ID_218752807 m1A Human chr5 - 675451 675442 675451 CTGGCCACACTGCACCCCCTGTGCTGCACCCCAGCCACACTGCACCCACCGTGCTGCACCCCTGG CTGGCCACACTGCACCCCCTGTGCTGCACCCC_________GCACCCACCGTGCTGCACCCCTGG CAGTGTGGCT C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:675068..675695 26863196 MeRIP-seq:(Medium) rs1365165253 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56065 RMVar_ID_56065 Human_SNP_ID_218752815 m1A Human chr5 - 675456 675456 675456 TACCCCTGGCCACACTGCACCCCCTGTGCTGCACCCCAGCCACACTGCACCCACCGTGCTGCACC TACCCCTGGCCACACTGCACCCCCTGTGCTGCCCCCCAGCCACACTGCACCCACCGTGCTGCACC T G TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:675256..675558 26863196 MeRIP-seq:(Medium) rs953881242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 56066 RMVar_ID_56066 Human_SNP_ID_218752884 m1A Human chr5 + 675516 675516 675516 GGGTACATTGTGGCCGGGGCTGCAGTGTGACCAGGGGTGCAGTGTGGCCGGGGATGCCGTGTGGC GGGTACATTGTGGCCGGGGCTGCAGTGTGACCGGGGGTGCAGTGTGGCCGGGGATGCCGTGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:674905..675678 26863196 MeRIP-seq:(Medium) rs916669205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24113849 56067 RMVar_ID_56067 Human_SNP_ID_218759102 m1A Human chr5 - 694253 694253 694253 CCCAGCACCCAGCACCACAGAACCGCCCTGTCATCTCGGCCCCGGAACCTTGTGGGGAGCCAACT CCCAGCACCCAGCACCACAGAACCGCCCTGTCGTCTCGGCCCCGGAACCTTGTGGGGAGCCAACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:694205..694285 26863196 MeRIP-seq:(Medium) rs1349523467 Functional Loss SNV dbSNP153 33..33 33 - - - 56068 RMVar_ID_56068 Human_SNP_ID_218792644 m1A Human chr5 - 795987 795987 795987 AGTACTGAGAAATGGGAGTACACTACTGAGAAATGGGAGCACAGTACTGGGAAATGGGCATACAG AGTACTGAGAAATGGGAGTACACTACTGAGAAGTGGGAGCACAGTACTGGGAAATGGGCATACAG T C ZDHHC11 Ensembl:ENSG00000188818 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:795967..796051 26863196 MeRIP-seq:(Medium) rs1369296882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78700,Human_RBP_ID_15528573 Human_Splice_Rec_631650 Human_miRNA_ID_587058 RMVar_hsa_circ_229976 56069 RMVar_ID_56069 Human_SNP_ID_218809594 m1A Human chr5 + 848969 848954 848969 CCCTGCACACCCAGCCCTGCTCACCCGAGCCCAGCTCACCCATGCCCGGCCCTGCTCACATGGCC CCCTGCACACCCAGCCCT_______________GCTCACCCATGCCCGGCCCTGCTCACATGGCC TGCTCACCCGAGCCCA T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:848920..849117 26863196 MeRIP-seq:(Medium) rs1360365826 Functional Loss DEL dbSNP153 19..33 33 - - - 56070 RMVar_ID_56070 Human_SNP_ID_218811389 m1A Human chr5 + 853164 853164 853164 ACAGACCCCACGGAGGACAGCGAGCCAGGGAGACAGACCCCACAGAGGACAGCGAGCCAGGGGGC ACAGACCCCACGGAGGACAGCGAGCCAGGGAGGCAGACCCCACAGAGGACAGCGAGCCAGGGGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:853113..853226 26863196 MeRIP-seq:(Medium) rs976336321 Functional Loss SNV dbSNP153 33..33 33 - - - 56071 RMVar_ID_56071 Human_SNP_ID_218812906 m1A Human chr5 + 856200 856196 856201 ACCACACAGACCACGTACCACACACACCACACACCACACAACACAGACCACACTGACCACACACC ACCACACAGACCACGTACCACACACACCA_____CACACAACACAGACCACACTGACCACACACC ACACAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:856149..856317 26863196 MeRIP-seq:(Medium) rs1468365685 Functional Loss DEL dbSNP153 30..34 33 - - - 56072 RMVar_ID_56072 Human_SNP_ID_218812912 m1A Human chr5 + 856205 856205 856205 ACAGACCACGTACCACACACACCACACACCACACAACACAGACCACACTGACCACACACCGCATA ACAGACCACGTACCACACACACCACACACCACGCAACACAGACCACACTGACCACACACCGCATA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:856111..856625 26863196 MeRIP-seq:(Medium) rs1234506652 Functional Loss SNV dbSNP153 33..33 33 - - - 56073 RMVar_ID_56073 Human_SNP_ID_218813187 m1A Human chr5 + 856911 856911 856911 CAAAATACCACACATACACCAAACCACACACCACACACACACCAAACCACACACCACCGAGCACA CAAAATACCACACATACACCAAACCACACACCTCACACACACCAAACCACACACCACCGAGCACA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:856769..857096 26863196 MeRIP-seq:(Medium) rs977065134 Functional Loss SNV dbSNP153 33..33 33 - - - 56074 RMVar_ID_56074 Human_SNP_ID_218813693 m1A Human chr5 + 858272 858272 858272 CCAGAGTCTGTCCTGGTCCCCATCCTGTCTTTATGACACCAGGCCCCTAGAGTCTGTCCAGGTCC CCAGAGTCTGTCCTGGTCCCCATCCTGTCTTTGTGACACCAGGCCCCTAGAGTCTGTCCAGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:858221..858296 26863196 MeRIP-seq:(Medium) rs1275236826 Functional Loss SNV dbSNP153 33..33 33 - - - 56075 RMVar_ID_56075 Human_SNP_ID_218813801 m1A Human chr5 - 858533 858533 858533 GAGTGTCATAAGGGCAGGGACGGTGAGGACAGACTCAGGGACCACAGTGTCATAAAGGAAGGACA GAGTGTCATAAGGGCAGGGACGGTGAGGACAGGCTCAGGGACCACAGTGTCATAAAGGAAGGACA T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:858483..858673 26863196 MeRIP-seq:(Medium) rs1422790242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3784038,Human_RBP_ID_5655535,Human_RBP_ID_7481169,Human_RBP_ID_15537215,Human_RBP_ID_18848520,Human_RBP_ID_18955828,Human_RBP_ID_24120105,Human_RBP_ID_27842181 56076 RMVar_ID_56076 Human_SNP_ID_218814526 m1A Human chr5 - 860942 860938 860942 GATGTGTATGAGGTACAGGTATTGGGTGTGTGAGTGTGTATGGGGTGCAGGTGGGTGTGTGGGTG GATGTGTATGAGGTACAGGTATTGGGTGTGTG____TGTATGGGGTGCAGGTGGGTGTGTGGGTG ACACT A BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:860728..861114 26863196 MeRIP-seq:(Medium) rs1253501136 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_648075,Human_RBP_ID_5655539,Human_RBP_ID_21989535,Human_RBP_ID_24120193 56077 RMVar_ID_56077 Human_SNP_ID_218814528 m1A Human chr5 - 860942 860942 860942 GATGTGTATGAGGTACAGGTATTGGGTGTGTGAGTGTGTATGGGGTGCAGGTGGGTGTGTGGGTG GATGTGTATGAGGTACAGGTATTGGGTGTGTGTGTGTGTATGGGGTGCAGGTGGGTGTGTGGGTG T A BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:860728..861114 26863196 MeRIP-seq:(Medium) rs112955365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_648075,Human_RBP_ID_5655539,Human_RBP_ID_21989535,Human_RBP_ID_24120193 56078 RMVar_ID_56078 Human_SNP_ID_218814529 m1A Human chr5 - 860942 860942 860942 GATGTGTATGAGGTACAGGTATTGGGTGTGTGAGTGTGTATGGGGTGCAGGTGGGTGTGTGGGTG GATGTGTATGAGGTACAGGTATTGGGTGTGTGGGTGTGTATGGGGTGCAGGTGGGTGTGTGGGTG T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:860728..861114 26863196 MeRIP-seq:(Medium) rs112955365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_648075,Human_RBP_ID_5655539,Human_RBP_ID_21989535,Human_RBP_ID_24120193 56079 RMVar_ID_56079 Human_SNP_ID_218815657 m1A Human chr5 + 864319 864319 864319 CAGGGTTCGTGGGGCTTGGAGACTCTGCTGACATGATACCACAGACAATTCATTACCTCCCCGCG CAGGGTTCGTGGGGCTTGGAGACTCTGCTGACGTGATACCACAGACAATTCATTACCTCCCCGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:864270..864360 26863196 MeRIP-seq:(Medium) rs760544747 Functional Loss SNV dbSNP153 33..33 33 - - - 56080 RMVar_ID_56080 Human_SNP_ID_218815702 m1A Human chr5 - 864452 864452 864452 CCTCTGCCAAGACCTAACTCTAGACCACCTTCAGCTCTTTTATTTTATTTTTTTAGTTTTATTTT CCTCTGCCAAGACCTAACTCTAGACCACCTTCTGCTCTTTTATTTTATTTTTTTAGTTTTATTTT T A BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:864401..864525 26863196 MeRIP-seq:(Medium) rs758090084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7481276,Human_RBP_ID_18848619,Human_RBP_ID_23049116,Human_RBP_ID_27517679 Human_miRNA_ID_1987975,Human_miRNA_ID_2372657 RMVar_hsa_circ_83066,RMVar_hsa_circ_229987 56081 RMVar_ID_56081 Human_SNP_ID_218820566 m1A Human chr5 - 881157 881157 881157 CTTCCAGATGGGCTATCTGAAGAGGAACGGGGACGGGAGCCTGCTCTACAGCGTGGTCAACACGG CTTCCAGATGGGCTATCTGAAGAGGAACGGGGGCGGGAGCCTGCTCTACAGCGTGGTCAACACGG T C BRD9 Ensembl:ENSG00000028310 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:881107..881178 26863196 MeRIP-seq:(Medium) rs1460679797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249716,Human_RBP_ID_787309,Human_RBP_ID_944015,Human_RBP_ID_2001489,Human_RBP_ID_5611291,Human_RBP_ID_7483446,Human_RBP_ID_8624296,Human_RBP_ID_15542969,Human_RBP_ID_17157416,Human_RBP_ID_18848869,Human_RBP_ID_19015452,Human_RBP_ID_22553217,Human_RBP_ID_22680261,Human_RBP_ID_23050335,Human_RBP_ID_23120180 Human_Splice_Rec_631745,Human_Splice_Rec_631772,Human_Splice_Rec_631773,Human_Splice_Rec_631798,Human_Splice_Rec_631799,Human_Splice_Rec_631824,Human_Splice_Rec_631825,Human_Splice_Rec_631850,Human_Splice_Rec_631851,Human_Splice_Rec_631876,Human_Splice_Rec_631877,Human_Splice_Rec_631940,Human_Splice_Rec_631941 RMVar_hsa_circ_77920,RMVar_hsa_circ_80144,RMVar_hsa_circ_229988,RMVar_hsa_circ_318436,RMVar_hsa_circ_350896,RMVar_hsa_circ_315397,RMVar_hsa_circ_110512,RMVar_hsa_circ_229990,RMVar_hsa_circ_229991,RMVar_hsa_circ_35476,RMVar_hsa_circ_38893,RMVar_hsa_circ_43392,RMVar_hsa_circ_81282,RMVar_hsa_circ_229992,RMVar_hsa_circ_40662,RMVar_hsa_circ_229993,RMVar_hsa_circ_13903 56082 RMVar_ID_56082 Human_SNP_ID_218820989 m1A Human chr5 + 882479 882479 882479 GACAACTGCCCAACACGTGAGCCACGCAGACCACAACCTCCCAACACGTGAGCCACACAGACCAC GACAACTGCCCAACACGTGAGCCACGCAGACCGCAACCTCCCAACACGTGAGCCACACAGACCAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:882395..882598 26863196 MeRIP-seq:(Medium) rs1250806019 Functional Loss SNV dbSNP153 33..33 33 - - - 56083 RMVar_ID_56083 Human_SNP_ID_218821097 m1A Human chr5 - 882798 882798 882798 AAGTTGCTGTGGTCTCTGGCTTATGTGTTGGGAAGTTGCTGTGGTTTGCGTGGCTCGTGTGTTGG AAGTTGCTGTGGTCTCTGGCTTATGTGTTGGGGAGTTGCTGTGGTTTGCGTGGCTCGTGTGTTGG T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:882719..882843 26863196 MeRIP-seq:(Medium) rs1372047464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1109433,Human_RBP_ID_3782681,Human_RBP_ID_9182044,Human_RBP_ID_17301853,Human_RBP_ID_22482124,Human_RBP_ID_23116178,Human_RBP_ID_24120945 RMVar_hsa_circ_80144,RMVar_hsa_circ_229988,RMVar_hsa_circ_318436,RMVar_hsa_circ_350896,RMVar_hsa_circ_315397,RMVar_hsa_circ_110512,RMVar_hsa_circ_229991,RMVar_hsa_circ_35476,RMVar_hsa_circ_38893,RMVar_hsa_circ_43392,RMVar_hsa_circ_81282,RMVar_hsa_circ_229992,RMVar_hsa_circ_40662,RMVar_hsa_circ_229993,RMVar_hsa_circ_13903 56084 RMVar_ID_56084 Human_SNP_ID_218821103 m1A Human chr5 + 882816 882816 882816 AAACCACAGCAACTTCCCAACACATAAGCCAGAGACCACAGCAACTTCCCAACACACGAGCCACG AAACCACAGCAACTTCCCAACACATAAGCCAGGGACCACAGCAACTTCCCAACACACGAGCCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:882266..883175;chr5:882201..883137 26863196 MeRIP-seq:(Medium) rs192051055 Functional Loss SNV dbSNP153 33..33 33 - - - 56085 RMVar_ID_56085 Human_SNP_ID_218821120 m1A Human chr5 + 882850 882850 882850 ACCACAGCAACTTCCCAACACACGAGCCACGCAGACTGCAACCTCCCAACACACAAGCCACACAA ACCACAGCAACTTCCCAACACACGAGCCACGCGGACTGCAACCTCCCAACACACAAGCCACACAA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:882300..883088 26863196 MeRIP-seq:(Medium) rs1560917107 Functional Loss SNV dbSNP153 33..33 33 - - - 56086 RMVar_ID_56086 Human_SNP_ID_218821281 m1A Human chr5 + 883343 883343 883343 GATATAGAGGTGAAATGAAACCTGCAAGGATTAATGTCACCTGCATTGCTCTACTTCTCTTATCA GATATAGAGGTGAAATGAAACCTGCAAGGATTCATGTCACCTGCATTGCTCTACTTCTCTTATCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:883341..886660 32194978 MeRIP-seq:(Medium) rs1207393454 Functional Loss SNV dbSNP153 33..33 33 - - - 56087 RMVar_ID_56087 Human_SNP_ID_218823827 m1A Human chr5 - 891267 891267 891267 TCTGCCGCCCAGGAAGAGAAGAAGCGGAAGCGAGAGAGGGAGCACTGTGACACGGAGGGAGAGGC TCTGCCGCCCAGGAAGAGAAGAAGCGGAAGCGGGAGAGGGAGCACTGTGACACGGAGGGAGAGGC T C BRD9 Ensembl:ENSG00000028310 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:891151..891315;chr5:891151..891330;chr5:891176..891342 26863196 MeRIP-seq:(Medium) rs1254806243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249718,Human_RBP_ID_838466,Human_RBP_ID_942702,Human_RBP_ID_3967731,Human_RBP_ID_5531845,Human_RBP_ID_9397580,Human_RBP_ID_19014663,Human_RBP_ID_21215407,Human_RBP_ID_23050336,Human_RBP_ID_24547907,Human_RBP_ID_26350624,Human_RBP_ID_27826212 Human_Splice_Rec_631758,Human_Splice_Rec_631788,Human_Splice_Rec_631814,Human_Splice_Rec_631840,Human_Splice_Rec_631866,Human_Splice_Rec_631926,Human_Splice_Rec_631962 Human_miRNA_ID_1994926,Human_miRNA_ID_2227423,Human_miRNA_ID_2284913,Human_miRNA_ID_2287912,Human_miRNA_ID_2503400,Human_miRNA_ID_2955284 RMVar_hsa_circ_80144,RMVar_hsa_circ_229988,RMVar_hsa_circ_110512,RMVar_hsa_circ_81282,RMVar_hsa_circ_229992,RMVar_hsa_circ_229993 56088 RMVar_ID_56088 Human_SNP_ID_218823831 m1A Human chr5 - 891281 891281 891281 CTCACTCCCTTGACTCTGCCGCCCAGGAAGAGAAGAAGCGGAAGCGAGAGAGGGAGCACTGTGAC CTCACTCCCTTGACTCTGCCGCCCAGGAAGAGGAGAAGCGGAAGCGAGAGAGGGAGCACTGTGAC T C BRD9 Ensembl:ENSG00000028310 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:891151..891329 26863196 MeRIP-seq:(Medium) rs1472141224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12603,Human_RBP_ID_249718,Human_RBP_ID_838466,Human_RBP_ID_942702,Human_RBP_ID_3967731,Human_RBP_ID_5531845,Human_RBP_ID_19014663,Human_RBP_ID_19125207,Human_RBP_ID_23050336,Human_RBP_ID_24547907,Human_RBP_ID_26350624,Human_RBP_ID_27825225 Human_Splice_Rec_631758,Human_Splice_Rec_631788,Human_Splice_Rec_631814,Human_Splice_Rec_631840,Human_Splice_Rec_631866,Human_Splice_Rec_631926,Human_Splice_Rec_631962 Human_miRNA_ID_3116584 RMVar_hsa_circ_80144,RMVar_hsa_circ_229988,RMVar_hsa_circ_110512,RMVar_hsa_circ_81282,RMVar_hsa_circ_229992,RMVar_hsa_circ_229993 56089 RMVar_ID_56089 Human_SNP_ID_218824143 m1A Human chr5 - 892131 892131 892131 CGGGCTCCGGGGTTCCAGGTCCCTCTTAATCCATCTTCTTGAACGAGTAATGTGAACAACATCCC CGGGCTCCGGGGTTCCAGGTCCCTCTTAATCCGTCTTCTTGAACGAGTAATGTGAACAACATCCC T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:892129..892329 32194978 MeRIP-seq:(Medium) rs542654384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5397096,Human_RBP_ID_19127042 Human_Splice_Rec_631837 RMVar_hsa_circ_107807,RMVar_hsa_circ_229996 56090 RMVar_ID_56090 Human_SNP_ID_218824266 m1A Human chr5 - 892496 892476 892496 GGTCCTGGGCACCGGGCGAGGTCCTGGCCACGAGGGAGGGGTTCTGGGCACGCGGGAGGGGGTCC GGTCCTGGGCACCGGGCGAGGTCCTGGCCACG____________________CGGGAGGGGGTCC GCGTGCCCAGAACCCCTCCCT G BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:892396..892721 26863196 MeRIP-seq:(Medium) rs956027449 Functional Loss DEL dbSNP153 33..52 33 - - - Human_RBP_ID_4842899,Human_RBP_ID_9436836,Human_RBP_ID_18955830 Human_Splice_Rec_631959 56091 RMVar_ID_56091 Human_SNP_ID_218824275 m1A Human chr5 - 892496 892496 892496 GGTCCTGGGCACCGGGCGAGGTCCTGGCCACGAGGGAGGGGTTCTGGGCACGCGGGAGGGGGTCC GGTCCTGGGCACCGGGCGAGGTCCTGGCCACGGGGGAGGGGTTCTGGGCACGCGGGAGGGGGTCC T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:892396..892721 26863196 MeRIP-seq:(Medium) rs1313180396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4842899,Human_RBP_ID_9436836,Human_RBP_ID_18955830 Human_Splice_Rec_631959 56092 RMVar_ID_56092 Human_SNP_ID_218824496 m1A Human chr5 - 892946 892946 892946 GGACCCAACCAGGGCGCGGCCGCCGCCACCTCACGCCCAGCGTCGCCGCCACAGCCGCTGCCTCA GGACCCAACCAGGGCGCGGCCGCCGCCACCTCGCGCCCAGCGTCGCCGCCACAGCCGCTGCCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:892851..893131 26863196 MeRIP-seq:(Medium) rs1159047886 Functional Loss SNV dbSNP153 33..33 33 - - - 56093 RMVar_ID_56093 Human_SNP_ID_218824564 m1A Human chr5 + 893078 893078 893078 CGAGTCGCCAACGGTCCACGTGGAGGTGCATCAGCGCGGCAGCAGGTGAGCCGGACCTGTCCGAC CGAGTCGCCAACGGTCCACGTGGAGGTGCATCTGCGCGGCAGCAGGTGAGCCGGACCTGTCCGAC A T TRIP13 Ensembl:ENSG00000071539 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:892926..893100 32194978 MeRIP-seq:(Medium) rs1355304253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845602,Human_RBP_ID_8893036,Human_RBP_ID_9335140 Human_Splice_Rec_631965,Human_Splice_Rec_631981,Human_Splice_Rec_632005 56094 RMVar_ID_56094 Human_SNP_ID_218824570 m1A Human chr5 - 893092 893092 893092 TGCCCAGAGGATGTGTCGGACAGGTCCGGCTCACCTGCTGCCGCGCTGATGCACCTCCACGTGGA TGCCCAGAGGATGTGTCGGACAGGTCCGGCTCGCCTGCTGCCGCGCTGATGCACCTCCACGTGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:892926..893100 26863196 MeRIP-seq:(Medium) rs1258487193 Functional Loss SNV dbSNP153 33..33 33 - - - 56095 RMVar_ID_56095 Human_SNP_ID_218825088 m1A Human chr5 - 894778 894777 894778 TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAAAGAAGCCAAAACACACATAAATGATCTTAGTTC TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAA_GAAGCCAAAACACACATAAATGATCTTAGTTC CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:894776..894850 26863196 MeRIP-seq:(Medium) rs541160921 Functional Loss DEL dbSNP153 33..33 33 - - - 56096 RMVar_ID_56096 Human_SNP_ID_218825090 m1A Human chr5 - 894778 894778 894778 TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAAAGAAGCCAAAACACACATAAATGATCTTAGTTC TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAAGGAAGCCAAAACACACATAAATGATCTTAGTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:894776..894850 26863196 MeRIP-seq:(Medium) rs771033212 Functional Loss SNV dbSNP153 33..33 33 - - - 56097 RMVar_ID_56097 Human_SNP_ID_218829400 m1A Human chr5 + 912427 912427 912427 CCTGGTTTTGGTCACGGGGTCCACATGACGTCACGTTCTTGAGTCGCCTGTTGTGATGATAGGCA CCTGGTTTTGGTCACGGGGTCCACATGACGTCGCGTTCTTGAGTCGCCTGTTGTGATGATAGGCA A G TRIP13 Ensembl:ENSG00000071539 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:912423..912626 26863196 MeRIP-seq:(Medium) rs924436357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80924,RMVar_hsa_circ_230003,RMVar_hsa_circ_85630,RMVar_hsa_circ_230005,RMVar_hsa_circ_38160,RMVar_hsa_circ_26464 56098 RMVar_ID_56098 Human_SNP_ID_218854986 m1A Human chr5 + 1008865 1008865 1008865 CTGTCCCCGCGCCCTGCGCCCGGTGGCCCCCCACCTCCGCCCCGCGGCCGTACCTGGCGCCCCCT CTGTCCCCGCGCCCTGCGCCCGGTGGCCCCCCGCCTCCGCCCCGCGGCCGTACCTGGCGCCCCCT A G NKD2 Ensembl:ENSG00000145506 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1008801..1033545 26863196 MeRIP-seq:(Medium) rs940704797 Functional Loss SNV dbSNP153 33..33 33 - - - 56099 RMVar_ID_56099 Human_SNP_ID_218856899 m1A Human chr5 + 1015236 1015236 1015236 TTCGTACTGCACAGTCATCTGAGCTGTCAGCAAGCTCTCACTGGTTGGCAGTGCCCACAGCCTCC TTCGTACTGCACAGTCATCTGAGCTGTCAGCACGCTCTCACTGGTTGGCAGTGCCCACAGCCTCC A C NKD2 Ensembl:ENSG00000145506 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:1015230..1015314 26863410 MeRIP-seq:(Medium) rs918148748 Functional Loss SNV dbSNP153 33..33 33 - - - 56100 RMVar_ID_56100 Human_SNP_ID_218862674 m1A Human chr5 - 1032214 1032214 1032214 TTTGGGGAGGGAGGGCTGCGGGAGCTGCACTCACCCTGTAGGGGACACTGGTCCTCCCGGAAAGG TTTGGGGAGGGAGGGCTGCGGGAGCTGCACTCCCCCTGTAGGGGACACTGGTCCTCCCGGAAAGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1009488..1034174 32194978 MeRIP-seq:(Medium) rs1295820693 Functional Loss SNV dbSNP153 33..33 33 - - - 56101 RMVar_ID_56101 Human_SNP_ID_218863864 m1A Human chr5 + 1035360 1035360 1035360 GAATGAGTGAATGCTGAATGAAGGAGGGAGGGAGTGAGTAATGGCAGGACCCCCCTTTCAGACCG GAATGAGTGAATGCTGAATGAAGGAGGGAGGGGGTGAGTAATGGCAGGACCCCCCTTTCAGACCG A G NKD2 Ensembl:ENSG00000145506 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1035357..1035592 26863196 MeRIP-seq:(Medium) rs371384621 Functional Loss SNV dbSNP153 33..33 33 - - - 56102 RMVar_ID_56102 Human_SNP_ID_218864685 m1A Human chr5 + 1036973 1036967 1036973 CAGGCGGGCAGTGTGGACGGCGGGCAGTGTGGACAGCGAGCAGTGTGGATGGCAGGCAGGCAGTG CAGGCGGGCAGTGTGGACGGCGGGCAG______CAGCGAGCAGTGTGGATGGCAGGCAGGCAGTG GTGTGGA G NKD2 Ensembl:ENSG00000145506 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1036758..1037109 26863196 MeRIP-seq:(Medium) rs1461345190 Functional Loss DEL dbSNP153 28..33 33 - - - 56103 RMVar_ID_56103 Human_SNP_ID_218865398 m1A Human chr5 - 1038397 1038397 1038397 TGCCCTGAGGTCGCGGGCTGTGGTGTGCTGGGAGCGAGGTGTGCTTGGCAGTGGCGCTAGGACGG TGCCCTGAGGTCGCGGGCTGTGGTGTGCTGGGTGCGAGGTGTGCTTGGCAGTGGCGCTAGGACGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1038027..1038602 26863196 MeRIP-seq:(Medium) rs1434376511 Functional Loss SNV dbSNP153 33..33 33 - - - 56104 RMVar_ID_56104 Human_SNP_ID_218867444 m1A Human chr5 + 1042832 1042829 1042833 AATGAGTGGGTGTGTGAACGAGTGGGTGTGTGAATGAATGGGTGAGTTCGTGTGTGAATGAGTGG AATGAGTGGGTGTGTGAACGAGTGGGTGTG____TGAATGGGTGAGTTCGTGTGTGAATGAGTGG GTGAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1042781..1042878 26863196 MeRIP-seq:(Medium) rs372979514 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_24074331 56105 RMVar_ID_56105 Human_SNP_ID_218868567 m1A Human chr5 - 1044222 1044198 1044222 ACTCATTCACACACCCATTCACACACTAACTCACCCACTCATTCACACACTAACTCCCCCACTCA ACTCATTCACACACCCATTCACACACTAACTC________________________CCCCACTCA GGAGTTAGTGTGTGAATGAGTGGGT G lnc-SLC12A7-1,lnc-SLC12A7-1:2,lnc-SLC12A7-1:3,lnc-SLC12A7-1:4,lnc-SLC12A7-1:5,lnc-SLC12A7-1:6,lnc-SLC12A7-1:7,lnc-SLC12A7-1:8,lnc-SLC12A7-1:9,lnc-SLC12A7-1:10,lnc-SLC12A7-1:11 RNACentral:URS00008BFC43,RNACentral:URS00008B8B6B,RNACentral:URS00008B5826,RNACentral:URS00008BE8A7,RNACentral:URS00008B24FF,RNACentral:URS00008BCCE9,RNACentral:URS00008BB784,RNACentral:URS00008B930B,RNACentral:URS00008B3672,RNACentral:URS00008BBA56,RNACentral:URS00008B52C0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,intron,exon,intron,intron,intron,intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:1044212..1044351 26863196 MeRIP-seq:(Medium) rs1189602973 Functional Loss DEL dbSNP153 33..56 33 - - - 56106 RMVar_ID_56106 Human_SNP_ID_218868588 m1A Human chr5 - 1044222 1044222 1044222 ACTCATTCACACACCCATTCACACACTAACTCACCCACTCATTCACACACTAACTCCCCCACTCA ACTCATTCACACACCCATTCACACACTAACTCCCCCACTCATTCACACACTAACTCCCCCACTCA T G lnc-SLC12A7-1,lnc-SLC12A7-1:2,lnc-SLC12A7-1:3,lnc-SLC12A7-1:4,lnc-SLC12A7-1:5,lnc-SLC12A7-1:6,lnc-SLC12A7-1:7,lnc-SLC12A7-1:8,lnc-SLC12A7-1:9,lnc-SLC12A7-1:10,lnc-SLC12A7-1:11 RNACentral:URS00008BFC43,RNACentral:URS00008B8B6B,RNACentral:URS00008B5826,RNACentral:URS00008BE8A7,RNACentral:URS00008B24FF,RNACentral:URS00008BCCE9,RNACentral:URS00008BB784,RNACentral:URS00008B930B,RNACentral:URS00008B3672,RNACentral:URS00008BBA56,RNACentral:URS00008B52C0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,intron,exon,intron,intron,intron,intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:1044212..1044351 26863196 MeRIP-seq:(Medium) rs866470399 Functional Loss SNV dbSNP153 33..33 33 - - - 56107 RMVar_ID_56107 Human_SNP_ID_218869005 m1A Human chr5 - 1044684 1044681 1044685 ATTCACACACTAACTCACCCACTCATTCACACACTAACTCACCCATTCACACACGAACTCACTCA ATTCACACACTAACTCACCCACTCATTCACA____AACTCACCCATTCACACACGAACTCACTCA TAGTG T lnc-SLC12A7-1,lnc-SLC12A7-1:2,lnc-SLC12A7-1:3,lnc-SLC12A7-1:4,lnc-SLC12A7-1:5,lnc-SLC12A7-1:6,lnc-SLC12A7-1:7,lnc-SLC12A7-1:8 RNACentral:URS00008B8B6B,RNACentral:URS00008B5826,RNACentral:URS00008BE8A7,RNACentral:URS00008B24FF,RNACentral:URS00008BB784,RNACentral:URS00008B930B,RNACentral:URS00008B3672,RNACentral:URS00008B52C0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1044648..1044719 26863196 MeRIP-seq:(Medium) rs1192690712 Functional Loss DEL dbSNP153 32..35 33 - - - 56108 RMVar_ID_56108 Human_SNP_ID_218873739 m1A Human chr5 - 1051415 1051406 1051415 ACAGTGAGTTCCCCCGACAGCCCACGACAGCCAGGACTGCCCTCCCCACCCCACCCCACCCCAGG ACAGTGAGTTCCCCCGACAGCCCACGACAGCC_________CTCCCCACCCCACCCCACCCCAGG GGGCAGTCCT G SLC12A7 Ensembl:ENSG00000113504 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1051088..1052022 26863196 MeRIP-seq:(Medium) rs1176426623 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_27329848,Human_RBP_ID_27510324 Human_miRNA_ID_337787 56109 RMVar_ID_56109 Human_SNP_ID_218878609 m1A Human chr5 - 1063945 1063945 1063945 AGGTGTGGAGGAAGTGCCGGATGCGTATCTTCACCGTGGCCCAGGTGGACGACAACAGCATCCAG AGGTGTGGAGGAAGTGCCGGATGCGTATCTTCCCCGTGGCCCAGGTGGACGACAACAGCATCCAG T G SLC12A7 Ensembl:ENSG00000113504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1063840..1063961 26863196 MeRIP-seq:(Medium) rs1396159233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5531852,Human_RBP_ID_18471905,Human_RBP_ID_22771865,Human_RBP_ID_27825229 Human_Splice_Rec_632132,Human_Splice_Rec_632172,Human_Splice_Rec_632196 RMVar_hsa_circ_95778,RMVar_hsa_circ_7593,RMVar_hsa_circ_268702,RMVar_hsa_circ_123849,RMVar_hsa_circ_89436,RMVar_hsa_circ_307998,RMVar_hsa_circ_360709,RMVar_hsa_circ_230008,RMVar_hsa_circ_369606,RMVar_hsa_circ_121429,RMVar_hsa_circ_230009,RMVar_hsa_circ_230011,RMVar_hsa_circ_230012,RMVar_hsa_circ_230010 56110 RMVar_ID_56110 Human_SNP_ID_218882925 m1A Human chr5 - 1075346 1075346 1075346 TACCGCGGGTAAGCGCTGTCAGCCCCCCTTACAGACCCGGCGCACGGGAGGGCGGGCCCCTCTCA TACCGCGGGTAAGCGCTGTCAGCCCCCCTTACGGACCCGGCGCACGGGAGGGCGGGCCCCTCTCA T C SLC12A7 Ensembl:ENSG00000113504 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1075344..1075457 26863196 MeRIP-seq:(Medium) rs753317189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124256 RMVar_hsa_circ_95778,RMVar_hsa_circ_7593,RMVar_hsa_circ_123849,RMVar_hsa_circ_89436,RMVar_hsa_circ_230008,RMVar_hsa_circ_121429,RMVar_hsa_circ_115032,RMVar_hsa_circ_230011,RMVar_hsa_circ_230012,RMVar_hsa_circ_230010,RMVar_hsa_circ_230013 56111 RMVar_ID_56111 Human_SNP_ID_218883461 m1A Human chr5 + 1076659 1076659 1076659 CATCCACACTGCCCCACGCTCCAGGCCCATACACCCATCCCCAGGTCCCCGTCCTGTGGGGGCTC CATCCACACTGCCCCACGCTCCAGGCCCATACCCCCATCCCCAGGTCCCCGTCCTGTGGGGGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1076658..1076750 26863196 MeRIP-seq:(Medium) rs749670849 Functional Loss SNV dbSNP153 33..33 33 - - - 56112 RMVar_ID_56112 Human_SNP_ID_218892410 m1A Human chr5 + 1099230 1099230 1099230 AACCCCACCCCATGGGCCAAAGAGCAGCACCCAGATACCACGTGCCCTGAGGCAGGAGCAGGGTA AACCCCACCCCATGGGCCAAAGAGCAGCACCCCGATACCACGTGCCCTGAGGCAGGAGCAGGGTA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1099227..1099512 32194978 MeRIP-seq:(Medium) rs1291653020 Functional Loss SNV dbSNP153 33..33 33 - - - 56113 RMVar_ID_56113 Human_SNP_ID_218896372 m1A Human chr5 - 1111904 1111885 1111904 ACGAGACTGCCGAGCGGACGGAGGCTCCGGGCACCCCCGAGGGCCCCGAGCCCGAGCGCCCCAGC ACGAGACTGCCGAGCGGACGGAGGCTCCGGGC___________________CCGAGCGCCCCAGC GGCTCGGGGCCCTCGGGGGT G SLC12A7 Ensembl:ENSG00000113504 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1111899..1112020 26863196 MeRIP-seq:(Medium) rs1453557561 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_5326732,Human_RBP_ID_27510550 Human_Splice_Rec_632097 RMVar_hsa_circ_116634,RMVar_hsa_circ_230024 56114 RMVar_ID_56114 Human_SNP_ID_218896377 m1A Human chr5 - 1111904 1111904 1111904 ACGAGACTGCCGAGCGGACGGAGGCTCCGGGCACCCCCGAGGGCCCCGAGCCCGAGCGCCCCAGC ACGAGACTGCCGAGCGGACGGAGGCTCCGGGCCCCCCCGAGGGCCCCGAGCCCGAGCGCCCCAGC T G SLC12A7 Ensembl:ENSG00000113504 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1111899..1112020 26863196 MeRIP-seq:(Medium) rs939189939 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5326732,Human_RBP_ID_27510550 Human_Splice_Rec_632097 RMVar_hsa_circ_116634,RMVar_hsa_circ_230024 56115 RMVar_ID_56115 Human_SNP_ID_218909940 m1A Human chr5 + 1157734 1157724 1157734 CCCACACCTACTCACTCCTGTGCCACCTGCCCACACCTGCTCACACCTGTTCTCATCTGCTCACA CCCACACCTACTCACTCCTGTGC__________CACCTGCTCACACCTGTTCTCATCTGCTCACA CCACCTGCCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1157226..1157905 26863196 MeRIP-seq:(Medium) rs1038824190 Functional Loss DEL dbSNP153 24..33 33 - - - 56116 RMVar_ID_56116 Human_SNP_ID_218962358 m1A Human chr5 - 1318392 1318392 1318392 ACGAGTTTGGGGAGTCCTACGAGGAGAAGGCCACGCGGGCGCCCCACACGGACTGAAGGCCGCCC ACGAGTTTGGGGAGTCCTACGAGGAGAAGGCCCCGCGGGCGCCCCACACGGACTGAAGGCCGCCC T G CLPTM1L Ensembl:ENSG00000049656 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1318013..1318469 26863196 MeRIP-seq:(Medium) rs773633350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4807787,Human_RBP_ID_22099292 Human_Splice_Rec_632462,Human_Splice_Rec_632486,Human_Splice_Rec_632500,Human_Splice_Rec_632528,Human_Splice_Rec_632542,Human_Splice_Rec_632548,Human_Splice_Rec_632564 RMVar_hsa_circ_99023,RMVar_hsa_circ_102671,RMVar_hsa_circ_230030,RMVar_hsa_circ_230031 56117 RMVar_ID_56117 Human_SNP_ID_218962466 m1A Human chr5 - 1318721 1318721 1318721 GCCCGTGCAGCCTCCGGGTCCCCCCTTCAGCCATGGCAGCCCGTGCAGCCTCCGGGTCGTCCCTT GCCCGTGCAGCCTCCGGGTCCCCCCTTCAGCCGTGGCAGCCCGTGCAGCCTCCGGGTCGTCCCTT T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1318719..1318831 26863196 MeRIP-seq:(Medium) rs1028786648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99023,RMVar_hsa_circ_102671,RMVar_hsa_circ_230030,RMVar_hsa_circ_230031 56118 RMVar_ID_56118 Human_SNP_ID_218964167 m1A Human chr5 - 1323896 1323896 1323896 GTGTTTACAGAGGCTTGGCGTTTGGGCCTCTAACTGGAAGCCATCTTTGTTCCCTGCAGGCCATG GTGTTTACAGAGGCTTGGCGTTTGGGCCTCTAGCTGGAAGCCATCTTTGTTCCCTGCAGGCCATG T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1323894..1323994 32194978 MeRIP-seq:(Medium) rs1382129104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18832146,Human_RBP_ID_22552902,Human_RBP_ID_22680282,Human_RBP_ID_22745879 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_97945,RMVar_hsa_circ_80267,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_230033,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_107332,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_230039,RMVar_hsa_circ_230040,RMVar_hsa_circ_230041 56119 RMVar_ID_56119 Human_SNP_ID_218965422 m1A Human chr5 - 1327143 1327114 1327143 ATGGAATGTGCCTGTAGAGGAGGAGCTGGATGAAATGTGTCTGTAGAGGAGGAGCTGGATGGAAT ATGGAATGTGCCTGTAGAGGAGGAGCTGGATG_____________________________GAAT CCATCCAGCTCCTCCTCTACAGACACATTT C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1326626..1327262 26863196 MeRIP-seq:(Medium) rs1561234743 Functional Loss DEL dbSNP153 33..61 33 - - - Human_RBP_ID_24082783 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044 56120 RMVar_ID_56120 Human_SNP_ID_218965437 m1A Human chr5 - 1327143 1327143 1327143 ATGGAATGTGCCTGTAGAGGAGGAGCTGGATGAAATGTGTCTGTAGAGGAGGAGCTGGATGGAAT ATGGAATGTGCCTGTAGAGGAGGAGCTGGATGGAATGTGTCTGTAGAGGAGGAGCTGGATGGAAT T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1326626..1327262 26863196 MeRIP-seq:(Medium) rs866894228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24082783 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044 56121 RMVar_ID_56121 Human_SNP_ID_218965827 m1A Human chr5 + 1327944 1327944 1327944 TCTACAGACACATTCCATCCAGCTCCTCCTCGACAGACACATTCCATCCAGCTCCTCCTCTACAG TCTACAGACACATTCCATCCAGCTCCTCCTCGGCAGACACATTCCATCCAGCTCCTCCTCTACAG A G lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:1327876..1328000;chr5:1327876..1328050;chr5:1327876..1328025 26863196 MeRIP-seq:(Medium) rs1333939642 Functional Loss SNV dbSNP153 33..33 33 - - - 56122 RMVar_ID_56122 Human_SNP_ID_218966012 m1A Human chr5 + 1328470 1328467 1328471 TACAGACACATTTCATCCAGCTCCTCCTCTGCAGACACATTCCATCCAGCTCCTCCTCTACAGAC TACAGACACATTTCATCCAGCTCCTCCTCT____ACACATTCCATCCAGCTCCTCCTCTACAGAC TGCAG T lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:1328451..1328615 26863196 MeRIP-seq:(Medium) rs1443059739 Functional Loss DEL dbSNP153 31..34 33 - - - 56123 RMVar_ID_56123 Human_SNP_ID_218966015 m1A Human chr5 + 1328470 1328470 1328470 TACAGACACATTTCATCCAGCTCCTCCTCTGCAGACACATTCCATCCAGCTCCTCCTCTACAGAC TACAGACACATTTCATCCAGCTCCTCCTCTGCGGACACATTCCATCCAGCTCCTCCTCTACAGAC A G lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:1328451..1328615 26863196 MeRIP-seq:(Medium) rs1384199348 Functional Loss SNV dbSNP153 33..33 33 - - - 56124 RMVar_ID_56124 Human_SNP_ID_218966022 m1A Human chr5 - 1328478 1328478 1328478 TGAAATGTGTCTGTAGAGGAGGAGCTGGATGGAATGTGTCTGCAGAGGAGGAGCTGGATGAAATG TGAAATGTGTCTGTAGAGGAGGAGCTGGATGGCATGTGTCTGCAGAGGAGGAGCTGGATGAAATG T G CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:1328476..1328734 26863196 MeRIP-seq:(Medium) rs1297454646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24082809 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044 56125 RMVar_ID_56125 Human_SNP_ID_218966376 m1A Human chr5 - 1329010 1328990 1329011 GGCCTCTGCGGCCGTCATGCCTGTAGAGGAGGAGCTGGATGCAATGTCTCTGTAGAGGAGGAGCT GGCCTCTGCGGCCGTCATGCCTGTAGAGGAG_____________________TAGAGGAGGAGCT ACAGAGACATTGCATCCAGCTC A CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1329008..1329127 32194978 MeRIP-seq:(Medium) rs1561237814 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_17158750,Human_RBP_ID_27734333 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044 56126 RMVar_ID_56126 Human_SNP_ID_218967037 m1A Human chr5 - 1330781 1330781 1330781 GCAGGAGGAGGAAGACGTGTTGAATAAGCTGGAGTGGTTCTTAAGGTACAGCTGGGGAGGAAACA GCAGGAGGAGGAAGACGTGTTGAATAAGCTGGGGTGGTTCTTAAGGTACAGCTGGGGAGGAAACA T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1330779..1330886 32194978 MeRIP-seq:(Medium) rs1343075729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1644403,Human_RBP_ID_5242382 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_87005,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044,RMVar_hsa_circ_230045 56127 RMVar_ID_56127 Human_SNP_ID_218967118 m1A Human chr5 + 1331039 1331039 1331039 GAGAAAAACAACTTGTTCGGGTCTGATACTGGAGCCAAATGCTCCTCACTCCTAACCAACAGGAC GAGAAAAACAACTTGTTCGGGTCTGATACTGGGGCCAAATGCTCCTCACTCCTAACCAACAGGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1331034..1331295 26863196 MeRIP-seq:(Medium) rs1050555113 Functional Loss SNV dbSNP153 33..33 33 - - - 56128 RMVar_ID_56128 Human_SNP_ID_218970375 m1A Human chr5 - 1338946 1338946 1338946 AGTGCCCTGGATGAGCCAGTGTCCCACTGGCGACCGCGGCTGGCGCTGAACGTGATGGCGGACAA AGTGCCCTGGATGAGCCAGTGTCCCACTGGCGTCCGCGGCTGGCGCTGAACGTGATGGCGGACAA T A CLPTM1L Ensembl:ENSG00000049656 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1338813..1339052 26863196 MeRIP-seq:(Medium) rs775418068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9397593,Human_RBP_ID_18057518,Human_RBP_ID_27826215 Human_Splice_Rec_632436,Human_Splice_Rec_632437,Human_Splice_Rec_632464,Human_Splice_Rec_632465,Human_Splice_Rec_632506,Human_Splice_Rec_632507 Human_miRNA_ID_2397085 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_79677,RMVar_hsa_circ_87005,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044,RMVar_hsa_circ_112418,RMVar_hsa_circ_230045,RMVar_hsa_circ_98576,RMVar_hsa_circ_104636,RMVar_hsa_circ_230046,RMVar_hsa_circ_120955,RMVar_hsa_circ_230047,RMVar_hsa_circ_230049,RMVar_hsa_circ_25216,RMVar_hsa_circ_230048 56129 RMVar_ID_56129 Human_SNP_ID_218970391 m1A Human chr5 + 1338976 1338976 1338976 GGTCGCCAGTGGGACACTGGCTCATCCAGGGCACTCGTCGGCTTCTTCTCCGCCTCGATCTGCTG GGTCGCCAGTGGGACACTGGCTCATCCAGGGCGCTCGTCGGCTTCTTCTCCGCCTCGATCTGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:1338951..1338975 26863196 MeRIP-seq:(Medium) rs750001438 Functional Loss SNV dbSNP153 33..33 33 - - - 56130 RMVar_ID_56130 Human_SNP_ID_218971265 m1A Human chr5 - 1341621 1341621 1341621 TTACTGATAACAGGCTGTGCCTCTCCGTCAGAACGGACATGTCTTTCTCCACACAGGTGGGCGAT TTACTGATAACAGGCTGTGCCTCTCCGTCAGATCGGACATGTCTTTCTCCACACAGGTGGGCGAT T A CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1341619..1341898 26863196 MeRIP-seq:(Medium) rs375396849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98576,RMVar_hsa_circ_230049,RMVar_hsa_circ_25216 56131 RMVar_ID_56131 Human_SNP_ID_218971364 m1A Human chr5 - 1341826 1341826 1341826 CAGTTAATGTTTCTGTACCAAAGAAAACGAGAAACAATGGGACGCTGTATGCCTACATCTTCCTC CAGTTAATGTTTCTGTACCAAAGAAAACGAGACACAATGGGACGCTGTATGCCTACATCTTCCTC T G CLPTM1L Ensembl:ENSG00000049656 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:1341776..1341825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_631880,Human_RBP_ID_1987084,Human_RBP_ID_24503441 Human_Splice_Rec_632434,Human_Splice_Rec_632504 RMVar_hsa_circ_98576,RMVar_hsa_circ_71711,RMVar_hsa_circ_230049,RMVar_hsa_circ_25216 56132 RMVar_ID_56132 Human_SNP_ID_218972533 m1A Human chr5 - 1344841 1344841 1344841 GGCGGGCCGGGGGCGCCGGGCGCGGGGCCGCCATGTGGAGCGGCCGCAGCTCCTTCACCAGCTTG GGCGGGCCGGGGGCGCCGGGCGCGGGGCCGCCGTGTGGAGCGGCCGCAGCTCCTTCACCAGCTTG T C CLPTM1L Ensembl:ENSG00000049656 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:1344726..1345050 26863410 MeRIP-seq:(Medium) rs1400675623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967089,Human_RBP_ID_4845122,Human_RBP_ID_9335169,Human_RBP_ID_9354514,Human_RBP_ID_17671704,Human_RBP_ID_22459100 56133 RMVar_ID_56133 Human_SNP_ID_218972561 m1A Human chr5 + 1344889 1344889 1344889 GGCGCCCCCGGCCCGCCCGCCTCTCAGCCGCGAGCCCCGCCCGCCCGGCGCCCAGCCCGCCGCTC GGCGCCCCCGGCCCGCCCGCCTCTCAGCCGCGGGCCCCGCCCGCCCGGCGCCCAGCCCGCCGCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:1344621..1345075;chr5:1344618..1345075 26863196 MeRIP-seq:(Medium) rs1333036986 Functional Loss SNV dbSNP153 33..33 33 - - - 56134 RMVar_ID_56134 Human_SNP_ID_218972594 m1A Human chr5 + 1344998 1344998 1344998 CGCCGCGGGGGAACGAATGCGCCGCGCGCCGCAGACCGCCGGCCGCCCCGCATGCTCCGGCCCCG CGCCGCGGGGGAACGAATGCGCCGCGCGCCGCCGACCGCCGGCCGCCCCGCATGCTCCGGCCCCG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,untreat control chr5:1344776..1345034;chr5:1344901..1345075;chr5:1344844..1345099 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1309792445 Functional Loss SNV dbSNP153 33..33 33 - - - 56135 RMVar_ID_56135 Human_SNP_ID_219008979 m1A Human chr5 + 1463621 1463621 1463621 AAAGAGGCTCATGGCGGTGATGTCCACGCGGGAGGGGCCGCGTCTCTCCGCAACCCTGGGTCCTA AAAGAGGCTCATGGCGGTGATGTCCACGCGGGGGGGGCCGCGTCTCTCCGCAACCCTGGGTCCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1463575..1463672 26863196 MeRIP-seq:(Medium) rs201791284 Functional Loss SNV dbSNP153 33..33 33 - - - 56136 RMVar_ID_56136 Human_SNP_ID_219010553 m1A Human chr5 - 1466855 1466855 1466855 TACGGAGCGCAAGAGGACGGCAGCGTCGGCGAAGGTGACCTGTCCTGCATCCTCAAGACGGCCCT TACGGAGCGCAAGAGGACGGCAGCGTCGGCGAGGGTGACCTGTCCTGCATCCTCAAGACGGCCCT T C LPCAT1 Ensembl:ENSG00000153395 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1466804..1466936 26863196 MeRIP-seq:(Medium) rs375037785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78402,Human_RBP_ID_634580,Human_RBP_ID_944046,Human_RBP_ID_8886070,Human_RBP_ID_9398871,Human_RBP_ID_19014692 Human_Splice_Rec_632718,Human_Splice_Rec_632750,Human_Splice_Rec_632754 Human_miRNA_ID_169298,Human_miRNA_ID_1024947 56137 RMVar_ID_56137 Human_SNP_ID_219011073 m1A Human chr5 + 1468086 1468086 1468086 CCACCGGCTCCTCCTTGCGGTGCTCAGGGAAGAAACGCTGACGCCTCCAGCCTTCCGGCCTGGCA CCACCGGCTCCTCCTTGCGGTGCTCAGGGAAGGAACGCTGACGCCTCCAGCCTTCCGGCCTGGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1467526..1468264 26863196 MeRIP-seq:(Medium) rs1269403872 Functional Loss SNV dbSNP153 33..33 33 - - - 56138 RMVar_ID_56138 Human_SNP_ID_219011852 m1A Human chr5 + 1470797 1470797 1470797 GGTGCTGACGTGACTGCACCGCCCTGTCCCCCAGTCAAACCCATGTGAACTCTGCACTCACCTTG GGTGCTGACGTGACTGCACCGCCCTGTCCCCCGGTCAAACCCATGTGAACTCTGCACTCACCTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1470793..1470864 26863196 MeRIP-seq:(Medium) rs774595322 Functional Loss SNV dbSNP153 33..33 33 - - - 56139 RMVar_ID_56139 Human_SNP_ID_219013427 m1A Human chr5 + 1475886 1475817 1475886 CCCTCCCATCTCCACTCCGAGTGGGGCTGCACAGGCCCCGCCCAGGCCCAGGAGTCCGAGGCTGC _________________________________GGCCCCGCCCAGGCCCAGGAGTCCGAGGCTGC CGGCCCCGCCCAGGCCCAGGAGTCCGAGGCTGCTTCTCCCTCCCATCTCCACTCCGAGTGGGGCTGCACA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1475651..1475975 26863196 MeRIP-seq:(Medium) rs1560957853 Functional Loss DEL dbSNP153 1..33 33 - - - 56140 RMVar_ID_56140 Human_SNP_ID_219013450 m1A Human chr5 + 1475886 1475885 1475886 CCCTCCCATCTCCACTCCGAGTGGGGCTGCACAGGCCCCGCCCAGGCCCAGGAGTCCGAGGCTGC CCCTCCCATCTCCACTCCGAGTGGGGCTGCAC_GGCCCCGCCCAGGCCCAGGAGTCCGAGGCTGC CA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1475651..1475975 26863196 MeRIP-seq:(Medium) rs34226286 Functional Loss DEL dbSNP153 33..33 33 - - - 56141 RMVar_ID_56141 Human_SNP_ID_219013911 m1A Human chr5 - 1477453 1477453 1477453 TCCTTCCTGTGTACAGCCCTTCTGAGGAGGAGAAGAGGAACCCCGCGCTGTATGCCAGCAACGTG TCCTTCCTGTGTACAGCCCTTCTGAGGAGGAGGAGAGGAACCCCGCGCTGTATGCCAGCAACGTG T C LPCAT1 Ensembl:ENSG00000153395 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1477374..1477522 26863196 MeRIP-seq:(Medium) rs767655718 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_75971,Human_RBP_ID_634720,Human_RBP_ID_840166,Human_RBP_ID_942728,Human_RBP_ID_3967091,Human_RBP_ID_9172396,Human_RBP_ID_19015503,Human_RBP_ID_22680287,Human_RBP_ID_22827557,Human_RBP_ID_27076120 Human_Splice_Rec_632710,Human_Splice_Rec_632711,Human_Splice_Rec_632742,Human_Splice_Rec_632743 RMVar_hsa_circ_5829,RMVar_hsa_circ_123845,RMVar_hsa_circ_116240,RMVar_hsa_circ_121576,RMVar_hsa_circ_230051,RMVar_hsa_circ_230052,RMVar_hsa_circ_80455,RMVar_hsa_circ_309220,RMVar_hsa_circ_230053,RMVar_hsa_circ_10251,RMVar_hsa_circ_41833,RMVar_hsa_circ_230054 56142 RMVar_ID_56142 Human_SNP_ID_219014583 m1A Human chr5 + 1479915 1479915 1479915 AACACCTGCTTATGTCCTTGGTTCGTCTAGCAAGACACCATCTCCTGCTTGTTCTCCAGCTCAGG AACACCTGCTTATGTCCTTGGTTCGTCTAGCAGGACACCATCTCCTGCTTGTTCTCCAGCTCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1479910..1480193 26863196 MeRIP-seq:(Medium) rs1329141934 Functional Loss SNV dbSNP153 33..33 33 - - - 56143 RMVar_ID_56143 Human_SNP_ID_219014634 m1A Human chr5 + 1480147 1480147 1480147 GAGCTGCTCCCAGGGCCACACTCACGCCTCCGACAGCCCAGTGCCCCAACCCTCTTTCTGCCCTG GAGCTGCTCCCAGGGCCACACTCACGCCTCCGCCAGCCCAGTGCCCCAACCCTCTTTCTGCCCTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1479898..1480185 26863196 MeRIP-seq:(Medium) rs1035138538 Functional Loss SNV dbSNP153 33..33 33 - - - 56144 RMVar_ID_56144 Human_SNP_ID_219025298 m1A Human chr5 + 1515360 1515360 1515360 GAACTGGCTGCAGATACAGGGAGCCCCCCAGCACATCCTGGCCCAAACCCTCAAAAGCTGCAGGA GAACTGGCTGCAGATACAGGGAGCCCCCCAGCTCATCCTGGCCCAAACCCTCAAAAGCTGCAGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1515357..1515859 26863196 MeRIP-seq:(Medium) rs1430759989 Functional Loss SNV dbSNP153 33..33 33 - - - 56145 RMVar_ID_56145 Human_SNP_ID_219027838 m1A Human chr5 - 1523844 1523844 1523844 CTCGGCTGCGCTCGCCGCGGGACGGCGCGGCCATGAGGCTGCGGGGATGCGGACCCCGGGCCGCC CTCGGCTGCGCTCGCCGCGGGACGGCGCGGCCCTGAGGCTGCGGGGATGCGGACCCCGGGCCGCC T G LPCAT1 Ensembl:ENSG00000153395 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:1523751..1523925 26863410 MeRIP-seq:(Medium) rs1237544087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4818765,Human_RBP_ID_18425087,Human_RBP_ID_22459105,Human_RBP_ID_27513095 RMVar_hsa_circ_121576,RMVar_hsa_circ_230054 56146 RMVar_ID_56146 Human_SNP_ID_219031705 m1A Human chr5 - 1539608 1539559 1539609 TGACCCCGTGTGGCCCTGTGTGACCCTGTGTGACCCTGTGTGACCCTGTGTGGCCCCCTATGGCC TGACCCCGTGTGGCCCTGTGTGACCCTGTGT__________________________________ TACACAGGGCCACACAGGGCCATAGGGGGCCACACAGGGTCACACAGGGTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1539572..1539750 26863196 MeRIP-seq:(Medium) rs1561006462 Functional Loss DEL dbSNP153 32..65 33 - - - 56147 RMVar_ID_56147 Human_SNP_ID_219031754 m1A Human chr5 - 1539608 1539608 1539608 TGACCCCGTGTGGCCCTGTGTGACCCTGTGTGACCCTGTGTGACCCTGTGTGGCCCCCTATGGCC TGACCCCGTGTGGCCCTGTGTGACCCTGTGTGGCCCTGTGTGACCCTGTGTGGCCCCCTATGGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1539572..1539750 26863196 MeRIP-seq:(Medium) rs906061658 Functional Loss SNV dbSNP153 33..33 33 - - - 56148 RMVar_ID_56148 Human_SNP_ID_219031755 m1A Human chr5 - 1539608 1539608 1539608 TGACCCCGTGTGGCCCTGTGTGACCCTGTGTGACCCTGTGTGACCCTGTGTGGCCCCCTATGGCC TGACCCCGTGTGGCCCTGTGTGACCCTGTGTGCCCCTGTGTGACCCTGTGTGGCCCCCTATGGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1539572..1539750 26863196 MeRIP-seq:(Medium) rs906061658 Functional Loss SNV dbSNP153 33..33 33 - - - 56149 RMVar_ID_56149 Human_SNP_ID_219032051 m1A Human chr5 + 1540085 1540085 1540085 ACAGGGCCACACAGAGCCACACGGGGCCACACAGGGTCACACAGAGCCACACGGGGTCACACAGA ACAGGGCCACACAGAGCCACACGGGGCCACACGGGGTCACACAGAGCCACACGGGGTCACACAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1540036..1540160 26863196 MeRIP-seq:(Medium) rs1279852147 Functional Loss SNV dbSNP153 33..33 33 - - - 56150 RMVar_ID_56150 Human_SNP_ID_219041360 m1A Human chr5 - 1570775 1570775 1570775 GCATTACTGTGAGCTCCGCCTCCTGCCAGAGCATTACTGTGTGAACTCCAACCCCTGCCAGAGCA GCATTACTGTGAGCTCCGCCTCCTGCCAGAGCTTTACTGTGTGAACTCCAACCCCTGCCAGAGCA T A SDHAP3 Ensembl:ENSG00000185986 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:1570758..1570955 26863196 MeRIP-seq:(Medium) rs1275771688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1991180,Human_RBP_ID_15362300 56151 RMVar_ID_56151 Human_SNP_ID_219041468 m1A Human chr5 + 1570983 1570953 1570984 CTCAGAGTAATGCTCTGGCAGGGGCGGAGCTCAGAGAGTAATGCTCTGGCAGGGGTTGGAATTCA CTC_______________________________AGAGTAATGCTCTGGCAGGGGTTGGAATTCA CAGAGTAATGCTCTGGCAGGGGCGGAGCTCAG C lnc-NDUFS6-18 RNACentral:URS00008B597B lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:1570890..1571098 26863196 MeRIP-seq:(Medium) rs1165108720 Functional Loss DEL dbSNP153 4..34 33 - - - 56152 RMVar_ID_56152 Human_SNP_ID_219041482 m1A Human chr5 + 1570983 1570982 1570984 CTCAGAGTAATGCTCTGGCAGGGGCGGAGCTCAGAGAGTAATGCTCTGGCAGGGGTTGGAATTCA CTCAGAGTAATGCTCTGGCAGGGGCGGAGCTC__AGAGTAATGCTCTGGCAGGGGTTGGAATTCA CAG C lnc-NDUFS6-18 RNACentral:URS00008B597B lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:1570890..1571098 26863196 MeRIP-seq:(Medium) rs1268147138 Functional Loss DEL dbSNP153 33..34 33 - - - 56153 RMVar_ID_56153 Human_SNP_ID_219054525 m1A Human chr5 + 1617804 1617804 1617804 TGGCCCTCAAACTGGAACATCAACTCCCCACCAGGTCTCCAGATGCACGGCCTGCAAACTGGAAC TGGCCCTCAAACTGGAACATCAACTCCCCACCCGGTCTCCAGATGCACGGCCTGCAAACTGGAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1617794..1617859 26863196 MeRIP-seq:(Medium) rs918708363 Functional Loss SNV dbSNP153 33..33 33 - - - 56154 RMVar_ID_56154 Human_SNP_ID_219054526 m1A Human chr5 + 1617804 1617804 1617804 TGGCCCTCAAACTGGAACATCAACTCCCCACCAGGTCTCCAGATGCACGGCCTGCAAACTGGAAC TGGCCCTCAAACTGGAACATCAACTCCCCACCGGGTCTCCAGATGCACGGCCTGCAAACTGGAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1617794..1617859 26863196 MeRIP-seq:(Medium) rs918708363 Functional Loss SNV dbSNP153 33..33 33 - - - 56155 RMVar_ID_56155 Human_SNP_ID_219054740 m1A Human chr5 + 1618459 1618459 1618459 ATTAGCTCCTACCCACCCGGGTCTCCAGCTCCACGACCCTCAACCGGCAACACTGGCTCCCCACC ATTAGCTCCTACCCACCCGGGTCTCCAGCTCCGCGACCCTCAACCGGCAACACTGGCTCCCCACC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1618359..1618488 26863196 MeRIP-seq:(Medium) rs1388469496 Functional Loss SNV dbSNP153 33..33 33 - - - 56156 RMVar_ID_56156 Human_SNP_ID_219054834 m1A Human chr5 - 1618701 1618701 1618701 AGCTGGAGACCTGGGTGGGGAGCTGATGTTCCAGTTCGAGGGCCATGAAGCTGGACACCCGGGGG AGCTGGAGACCTGGGTGGGGAGCTGATGTTCCTGTTCGAGGGCCATGAAGCTGGACACCCGGGGG T A AC026412.1 Ensembl:ENSG00000188002 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1618652..1618909 26863196 MeRIP-seq:(Medium) rs540326695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17158754 RMVar_hsa_circ_230059,RMVar_hsa_circ_89185 56157 RMVar_ID_56157 Human_SNP_ID_219054835 m1A Human chr5 - 1618701 1618701 1618701 AGCTGGAGACCTGGGTGGGGAGCTGATGTTCCAGTTCGAGGGCCATGAAGCTGGACACCCGGGGG AGCTGGAGACCTGGGTGGGGAGCTGATGTTCCGGTTCGAGGGCCATGAAGCTGGACACCCGGGGG T C AC026412.1 Ensembl:ENSG00000188002 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1618652..1618909 26863196 MeRIP-seq:(Medium) rs540326695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17158754 RMVar_hsa_circ_230059,RMVar_hsa_circ_89185 56158 RMVar_ID_56158 Human_SNP_ID_219054871 m1A Human chr5 + 1618802 1618802 1618802 GGTCTCCAGATGCACGGCCCTCAAACTGGAACATCAACTCCCCACCCAGGTCTCCAGCTCCACGG GGTCTCCAGATGCACGGCCCTCAAACTGGAACGTCAACTCCCCACCCAGGTCTCCAGCTCCACGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1618788..1618879 26863196 MeRIP-seq:(Medium) rs1180130323 Functional Loss SNV dbSNP153 33..33 33 - - - 56159 RMVar_ID_56159 Human_SNP_ID_219054872 m1A Human chr5 + 1618806 1618806 1618806 TCCAGATGCACGGCCCTCAAACTGGAACATCAACTCCCCACCCAGGTCTCCAGCTCCACGGCCCT TCCAGATGCACGGCCCTCAAACTGGAACATCAGCTCCCCACCCAGGTCTCCAGCTCCACGGCCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1618642..1619032 26863196 MeRIP-seq:(Medium) rs1320716559 Functional Loss SNV dbSNP153 33..33 33 - - - 56160 RMVar_ID_56160 Human_SNP_ID_219055059 m1A Human chr5 + 1619379 1619379 1619379 ATCAGCTCCCACCCACCCGGGTCTCCAGCTCCACGGCCCTCAACCGGCAACACTGGCTCCCCACC ATCAGCTCCCACCCACCCGGGTCTCCAGCTCCCCGGCCCTCAACCGGCAACACTGGCTCCCCACC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1619253..1619461 26863196 MeRIP-seq:(Medium) rs150363878 Functional Loss SNV dbSNP153 33..33 33 - - - 56161 RMVar_ID_56161 Human_SNP_ID_219057472 m1A Human chr5 + 1626763 1626763 1626763 TGTCATACTCTTATGGGGGGAGTGAAAAATTGAGGCCCAACATTAAATCACCCACGCAAGAAATG TGTCATACTCTTATGGGGGGAGTGAAAAATTGGGGCCCAACATTAAATCACCCACGCAAGAAATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1626759..1626888 26863196 MeRIP-seq:(Medium) rs1314176194 Functional Loss SNV dbSNP153 33..33 33 - - - 56162 RMVar_ID_56162 Human_SNP_ID_219068955 m1A Human chr5 - 1667281 1667280 1667281 GAGGACGAGAGGGGGGGAGGGGGGAGGAGGGGAGGGCGGCGCCGCGGGGAGGCCAGGAGTCCGCA GAGGACGAGAGGGGGGGAGGGGGGAGGAGGGG_GGGCGGCGCCGCGGGGAGGCCAGGAGTCCGCA CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:1667276..1667325 26863196 MeRIP-seq:(Medium) rs1230018388 Functional Loss DEL dbSNP153 33..33 33 - - - 56163 RMVar_ID_56163 Human_SNP_ID_219068956 m1A Human chr5 - 1667281 1667281 1667281 GAGGACGAGAGGGGGGGAGGGGGGAGGAGGGGAGGGCGGCGCCGCGGGGAGGCCAGGAGTCCGCA GAGGACGAGAGGGGGGGAGGGGGGAGGAGGGGGGGGCGGCGCCGCGGGGAGGCCAGGAGTCCGCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:1667276..1667325 26863196 MeRIP-seq:(Medium) rs1459569760 Functional Loss SNV dbSNP153 33..33 33 - - - 56164 RMVar_ID_56164 Human_SNP_ID_219101170 m1A Human chr5 - 1787840 1787840 1787840 ACACTGAAGGCAGGTGCTGGGCACGTGGGTAAAGGCCATTTGGTCCACCGGAAGGCACTCCTCCT ACACTGAAGGCAGGTGCTGGGCACGTGGGTAAGGGCCATTTGGTCCACCGGAAGGCACTCCTCCT T C HSALNG0039592 RNACentral:URS0000EB2EB1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1787838..1787922 26863196 MeRIP-seq:(Medium) rs183037702 Functional Loss SNV dbSNP153 33..33 33 - - - 56165 RMVar_ID_56165 Human_SNP_ID_219104220 m1A Human chr5 - 1798760 1798760 1798760 GCGCTCACTTCTCTCACCCGGCCTCCTGCCCCATCTGCTGCCTGCGCTGGGGTTCAAAAACAAGA GCGCTCACTTCTCTCACCCGGCCTCCTGCCCCGTCTGCTGCCTGCGCTGGGGTTCAAAAACAAGA T C MRPL36 Ensembl:ENSG00000171421 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1798711..1798827 26863196 MeRIP-seq:(Medium) rs1443102874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640233,Human_RBP_ID_787513,Human_RBP_ID_1321071,Human_RBP_ID_4827224,Human_RBP_ID_5509431,Human_RBP_ID_9335171,Human_RBP_ID_18046263,Human_RBP_ID_18840446,Human_RBP_ID_21944499,Human_RBP_ID_22459106,Human_RBP_ID_22512211,Human_RBP_ID_24101236,Human_RBP_ID_27515004 RMVar_hsa_circ_98227,RMVar_hsa_circ_230061 56166 RMVar_ID_56166 Human_SNP_ID_219104223 m1A Human chr5 + 1798766 1798766 1798766 TTTTGAACCCCAGCGCAGGCAGCAGATGGGGCAGGAGGCCGGGTGAGAGAAGTGAGCGCACTGCT TTTTGAACCCCAGCGCAGGCAGCAGATGGGGCCGGAGGCCGGGTGAGAGAAGTGAGCGCACTGCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:1798584..1798933 32194978 MeRIP-seq:(Medium) rs775956445 Functional Loss SNV dbSNP153 33..33 33 - - - 56167 RMVar_ID_56167 Human_SNP_ID_219104224 m1A Human chr5 + 1798766 1798766 1798766 TTTTGAACCCCAGCGCAGGCAGCAGATGGGGCAGGAGGCCGGGTGAGAGAAGTGAGCGCACTGCT TTTTGAACCCCAGCGCAGGCAGCAGATGGGGCGGGAGGCCGGGTGAGAGAAGTGAGCGCACTGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:1798584..1798933 32194978 MeRIP-seq:(Medium) rs775956445 Functional Loss SNV dbSNP153 33..33 33 - - - 56168 RMVar_ID_56168 Human_SNP_ID_219104241 m1A Human chr5 - 1798798 1798798 1798798 GGTGCAGCCCCCGTGGCTGTGGAACCCGGGGCAGCAGTGCGCTCACTTCTCTCACCCGGCCTCCT GGTGCAGCCCCCGTGGCTGTGGAACCCGGGGCTGCAGTGCGCTCACTTCTCTCACCCGGCCTCCT T A MRPL36 Ensembl:ENSG00000171421 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr5:1798751..1798800;chr5:1798748..1798890 26863196 MeRIP-seq:(Medium) rs1473126533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640235,Human_RBP_ID_4854054,Human_RBP_ID_8612688,Human_RBP_ID_9335171,Human_RBP_ID_22459107,Human_RBP_ID_27080531,Human_RBP_ID_27335767 Human_miRNA_ID_2150819,Human_miRNA_ID_2419307 RMVar_hsa_circ_98227,RMVar_hsa_circ_230061 56169 RMVar_ID_56169 Human_SNP_ID_219104290 m1A Human chr5 - 1798878 1798878 1798878 TGGTGAACCCTCTGCTCTATCTCAGTCGTCACACGGTGAAGCCTCGAGCCCTCTCCACATTTCTA TGGTGAACCCTCTGCTCTATCTCAGTCGTCACTCGGTGAAGCCTCGAGCCCTCTCCACATTTCTA T A MRPL36 Ensembl:ENSG00000171421 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:1798876..1798925 26863196 MeRIP-seq:(Medium) rs778627177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640236,Human_RBP_ID_1652612,Human_RBP_ID_4854057,Human_RBP_ID_5427203,Human_RBP_ID_17662836,Human_RBP_ID_26525564,Human_RBP_ID_26826146,Human_RBP_ID_27335769,Human_RBP_ID_27515008 Human_Splice_Rec_632886,Human_Splice_Rec_632888,Human_Splice_Rec_632890,Human_Splice_Rec_632892,Human_Splice_Rec_632894 RMVar_hsa_circ_98227,RMVar_hsa_circ_230061 56170 RMVar_ID_56170 Human_SNP_ID_219104291 m1A Human chr5 - 1798878 1798878 1798878 TGGTGAACCCTCTGCTCTATCTCAGTCGTCACACGGTGAAGCCTCGAGCCCTCTCCACATTTCTA TGGTGAACCCTCTGCTCTATCTCAGTCGTCACGCGGTGAAGCCTCGAGCCCTCTCCACATTTCTA T C MRPL36 Ensembl:ENSG00000171421 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:1798876..1798925 26863196 MeRIP-seq:(Medium) rs778627177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640236,Human_RBP_ID_1652612,Human_RBP_ID_4854057,Human_RBP_ID_5427203,Human_RBP_ID_17662836,Human_RBP_ID_26525564,Human_RBP_ID_26826146,Human_RBP_ID_27335769,Human_RBP_ID_27515008 Human_Splice_Rec_632886,Human_Splice_Rec_632888,Human_Splice_Rec_632890,Human_Splice_Rec_632892,Human_Splice_Rec_632894 RMVar_hsa_circ_98227,RMVar_hsa_circ_230061 56171 RMVar_ID_56171 Human_SNP_ID_219104299 m1A Human chr5 + 1798891 1798888 1798892 AGGGCTCGAGGCTTCACCGTGTGACGACTGAGATAGAGCAGAGGGTTCACCATTTTCCTTATAAA AGGGCTCGAGGCTTCACCGTGTGACGACTG____AGAGCAGAGGGTTCACCATTTTCCTTATAAA GAGAT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:1798876..1798925 26863196 MeRIP-seq:(Medium) rs751540502 Functional Loss DEL dbSNP153 31..34 33 - - - 56172 RMVar_ID_56172 Human_SNP_ID_219104560 m1A Human chr5 + 1799629 1799628 1799629 GTCGGGCGCCCACGGTCGGACCCGCACCCCCCAACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC GTCGGGCGCCCACGGTCGGACCCGCACCCCCC_ACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1799626..1799878 26863196 MeRIP-seq:(Medium) rs68123901 Functional Loss DEL dbSNP153 33..33 33 - - - 56173 RMVar_ID_56173 Human_SNP_ID_219104562 m1A Human chr5 + 1799629 1799628 1799630 GTCGGGCGCCCACGGTCGGACCCGCACCCCCCAACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC GTCGGGCGCCCACGGTCGGACCCGCACCCCCC__CCCTGGCCCTCTGAGACCGCCAGGCCCCGGC CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1799626..1799878 26863196 MeRIP-seq:(Medium) rs1196178182 Functional Loss DEL dbSNP153 33..34 33 - - - 56174 RMVar_ID_56174 Human_SNP_ID_219104563 m1A Human chr5 + 1799629 1799629 1799629 GTCGGGCGCCCACGGTCGGACCCGCACCCCCCAACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC GTCGGGCGCCCACGGTCGGACCCGCACCCCCCCACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1799626..1799878 26863196 MeRIP-seq:(Medium) rs61525327 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6664,GWAS_ID_6665,GWAS_ID_6666,GWAS_ID_6667,GWAS_ID_6668,GWAS_ID_6669,GWAS_ID_6670,GWAS_ID_6671,GWAS_ID_6672,GWAS_ID_6673,GWAS_ID_6674,GWAS_ID_6675,GWAS_ID_6676,GWAS_ID_6677,GWAS_ID_6678,GWAS_ID_6679,GWAS_ID_6680,GWAS_ID_6681,GWAS_ID_6682,GWAS_ID_6683,GWAS_ID_6684,GWAS_ID_6685,GWAS_ID_6686,GWAS_ID_6687,GWAS_ID_6688,GWAS_ID_6689,GWAS_ID_6690,GWAS_ID_6691,GWAS_ID_6692,GWAS_ID_6693,GWAS_ID_6694,GWAS_ID_6695 56175 RMVar_ID_56175 Human_SNP_ID_219104564 m1A Human chr5 + 1799629 1799629 1799629 GTCGGGCGCCCACGGTCGGACCCGCACCCCCCAACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC GTCGGGCGCCCACGGTCGGACCCGCACCCCCCGACCCTGGCCCTCTGAGACCGCCAGGCCCCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1799626..1799878 26863196 MeRIP-seq:(Medium) rs61525327 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6664,GWAS_ID_6665,GWAS_ID_6666,GWAS_ID_6667,GWAS_ID_6668,GWAS_ID_6669,GWAS_ID_6670,GWAS_ID_6671,GWAS_ID_6672,GWAS_ID_6673,GWAS_ID_6674,GWAS_ID_6675,GWAS_ID_6676,GWAS_ID_6677,GWAS_ID_6678,GWAS_ID_6679,GWAS_ID_6680,GWAS_ID_6681,GWAS_ID_6682,GWAS_ID_6683,GWAS_ID_6684,GWAS_ID_6685,GWAS_ID_6686,GWAS_ID_6687,GWAS_ID_6688,GWAS_ID_6689,GWAS_ID_6690,GWAS_ID_6691,GWAS_ID_6692,GWAS_ID_6693,GWAS_ID_6694,GWAS_ID_6695 56176 RMVar_ID_56176 Human_SNP_ID_219105378 m1A Human chr5 + 1801475 1801475 1801475 GGCTGCTGAACCGGTGTGGCGAGGCGGCGCGGAGCCTGCCCCTGGGCGCCAGGTGTTTCGGGGTG GGCTGCTGAACCGGTGTGGCGAGGCGGCGCGGTGCCTGCCCCTGGGCGCCAGGTGTTTCGGGGTG A T NDUFS6 Ensembl:ENSG00000145494 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:1801401..1802192 32194978 MeRIP-seq:(Medium) rs781202124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845130,Human_RBP_ID_5151070,Human_RBP_ID_5326484,Human_RBP_ID_5509434,Human_RBP_ID_9335172,Human_RBP_ID_18424924,Human_RBP_ID_22458789 Human_Splice_Rec_632895,Human_Splice_Rec_632901,Human_Splice_Rec_632905 RMVar_hsa_circ_100999,RMVar_hsa_circ_230062 56177 RMVar_ID_56177 Human_SNP_ID_219105430 m1A Human chr5 + 1801541 1801541 1801541 GGGTCTCGCCGACCGGGGAGAAGGTCACGCACACTGGCCAGGTAACGGCCGCTGGGTACAGGATG GGGTCTCGCCGACCGGGGAGAAGGTCACGCACGCTGGCCAGGTAACGGCCGCTGGGTACAGGATG A G NDUFS6 Ensembl:ENSG00000145494 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:1801500..1801613 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4845612,Human_RBP_ID_5326485,Human_RBP_ID_9335172,Human_RBP_ID_22458789 Human_Splice_Rec_632895,Human_Splice_Rec_632901,Human_Splice_Rec_632905 Human_miRNA_ID_2174677,Human_miRNA_ID_2178120,Human_miRNA_ID_2205786 RMVar_hsa_circ_100999,RMVar_hsa_circ_230062 56178 RMVar_ID_56178 Human_SNP_ID_219105694 m1A Human chr5 - 1802304 1802303 1802304 CTTTATCATCATAAACCTGGAAAAAAACAAAAAGACCATGTGTGACTTTTACGGCCTAATTCTGA CTTTATCATCATAAACCTGGAAAAAAACAAAA_GACCATGTGTGACTTTTACGGCCTAATTCTGA CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr5:1802301..1802325;chr5:1802301..1802400 26863196 MeRIP-seq:(Medium) rs773781708 Functional Loss DEL dbSNP153 33..33 33 - - - 56179 RMVar_ID_56179 Human_SNP_ID_219105700 m1A Human chr5 - 1802310 1802310 1802310 TGTAGTCTTTATCATCATAAACCTGGAAAAAAACAAAAAGACCATGTGTGACTTTTACGGCCTAA TGTAGTCTTTATCATCATAAACCTGGAAAAAACCAAAAAGACCATGTGTGACTTTTACGGCCTAA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:1802301..1802400 26863410 MeRIP-seq:(Medium) rs779909584 Functional Loss SNV dbSNP153 33..33 33 - - - 56180 RMVar_ID_56180 Human_SNP_ID_219105957 m1A Human chr5 + 1803122 1803122 1803122 CTTCTTGTTAACACCGTAGCTATCCCTAAATCATGTATTTTCCCTTCTCCTTCAATCTTGGTTAC CTTCTTGTTAACACCGTAGCTATCCCTAAATCGTGTATTTTCCCTTCTCCTTCAATCTTGGTTAC A G NDUFS6 Ensembl:ENSG00000145494 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:1802301..1814511 26863196 MeRIP-seq:(Medium) rs187125139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21087962 RMVar_hsa_circ_81273,RMVar_hsa_circ_100999,RMVar_hsa_circ_230062,RMVar_hsa_circ_230063 56181 RMVar_ID_56181 Human_SNP_ID_219106382 m1A Human chr5 - 1804944 1804944 1804944 AGAGGGAGGGATGAACAGGCAGAGCACAGAGGATTTTTAGGGCAGTGAACTCGGTACAACACTGT AGAGGGAGGGATGAACAGGCAGAGCACAGAGGGTTTTTAGGGCAGTGAACTCGGTACAACACTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:1804942..1805208 26863196 MeRIP-seq:(Medium) rs368760610 Functional Loss SNV dbSNP153 33..33 33 - - - 56182 RMVar_ID_56182 Human_SNP_ID_219108910 m1A Human chr5 - 1814391 1814391 1814391 CGCCGCCATCGCACGCTATCACCCGAGTCTCCACCTCGCTCACGGGCTGCTCTGCTATCAAATCA CGCCGCCATCGCACGCTATCACCCGAGTCTCCGCCTCGCTCACGGGCTGCTCTGCTATCAAATCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:1814292..1814500;chr5:1814300..1814495 26863196 MeRIP-seq:(Medium) rs111796257 Functional Loss SNV dbSNP153 33..33 33 - - - 56183 RMVar_ID_56183 Human_SNP_ID_219108941 m1A Human chr5 + 1814439 1814439 1814439 AGCGTGCGATGGCGGCGGGGGAGCTCTTGGCCACCCAAAAGTGTATATAAACTTGGTGCGTAGCT AGCGTGCGATGGCGGCGGGGGAGCTCTTGGCCCCCCAAAAGTGTATATAAACTTGGTGCGTAGCT A C NDUFS6 Ensembl:ENSG00000145494 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:1814390..1814536 32194978 MeRIP-seq:(Medium) rs1129775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640732,Human_RBP_ID_1041138,Human_RBP_ID_1321155,Human_RBP_ID_1391313,Human_RBP_ID_7426171,Human_RBP_ID_15418297,Human_RBP_ID_17662649,Human_RBP_ID_18056698,Human_RBP_ID_21900439,Human_RBP_ID_22458790,Human_RBP_ID_24102055 Human_Splice_Rec_632899 RMVar_hsa_circ_81273,RMVar_hsa_circ_100999,RMVar_hsa_circ_230062,RMVar_hsa_circ_84028,RMVar_hsa_circ_230063,RMVar_hsa_circ_230064 56184 RMVar_ID_56184 Human_SNP_ID_219109673 m1A Human chr5 - 1816700 1816700 1816700 TCCCACTCGCCTTCCCTCTCGCCTTCCCTCTCACCTTCCGTCTCACCTTCCCTCTTACCTTCCCT TCCCACTCGCCTTCCCTCTCGCCTTCCCTCTCGCCTTCCGTCTCACCTTCCCTCTTACCTTCCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1816599..1816984 26863196 MeRIP-seq:(Medium) rs1274065092 Functional Loss SNV dbSNP153 33..33 33 - - - 56185 RMVar_ID_56185 Human_SNP_ID_219109674 m1A Human chr5 - 1816700 1816700 1816700 TCCCACTCGCCTTCCCTCTCGCCTTCCCTCTCACCTTCCGTCTCACCTTCCCTCTTACCTTCCCT TCCCACTCGCCTTCCCTCTCGCCTTCCCTCTCCCCTTCCGTCTCACCTTCCCTCTTACCTTCCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1816599..1816984 26863196 MeRIP-seq:(Medium) rs1274065092 Functional Loss SNV dbSNP153 33..33 33 - - - 56186 RMVar_ID_56186 Human_SNP_ID_219112572 m1A Human chr5 + 1828060 1828059 1828060 AGCCGGAGCAGGTGGTGTGCAGGGAGAGGCGGAGCCGCGCGCAGGGAGGGGCGGAGCCGCGCGCA AGCCGGAGCAGGTGGTGTGCAGGGAGAGGCGG_GCCGCGCGCAGGGAGGGGCGGAGCCGCGCGCA GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:1828046..1828120;chr5:1828050..1828183 26863196 MeRIP-seq:(Medium) rs1157923999 Functional Loss DEL dbSNP153 33..33 33 - - - 56187 RMVar_ID_56187 Human_SNP_ID_220063470 m1A Human chr5 + 5305294 5305232 5305294 CAATCCCACACCACACACACACATCCCACACCACACACACACACATCCCACACCACACACACACA _________________________________CACACACACACATCCCACACCACACACACACA CCACACACACACAATCCCACACCACACACACAATCCCACACCACACACACACATCCCACACCA C ADAMTS16 Ensembl:ENSG00000145536 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:5305023..5305418 26863196 MeRIP-seq:(Medium) rs1561000646 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_2375,RMVar_hsa_circ_347044,RMVar_hsa_circ_24364,RMVar_hsa_circ_44129,RMVar_hsa_circ_23480,RMVar_hsa_circ_23749,RMVar_hsa_circ_30333,RMVar_hsa_circ_33426,RMVar_hsa_circ_41820 56188 RMVar_ID_56188 Human_SNP_ID_220063485 m1A Human chr5 + 5305294 5305253 5305294 CAATCCCACACCACACACACACATCCCACACCACACACACACACATCCCACACCACACACACACA _________________________________CACACACACACATCCCACACCACACACACACA CCACACACACAATCCCACACCACACACACACATCCCACACCA C ADAMTS16 Ensembl:ENSG00000145536 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:5305023..5305418 26863196 MeRIP-seq:(Medium) rs1561000682 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_2375,RMVar_hsa_circ_347044,RMVar_hsa_circ_24364,RMVar_hsa_circ_44129,RMVar_hsa_circ_23480,RMVar_hsa_circ_23749,RMVar_hsa_circ_30333,RMVar_hsa_circ_33426,RMVar_hsa_circ_41820 56189 RMVar_ID_56189 Human_SNP_ID_220348116 m1A Human chr5 - 6374334 6374334 6374334 AGCTAAAAATGAGCAAGTTAAAGGCAAGATCGACACCATGAAGGTAAGACTCTAAGGAGTGTCAG AGCTAAAAATGAGCAAGTTAAAGGCAAGATCGGCACCATGAAGGTAAGACTCTAAGGAGTGTCAG T C MED10 Ensembl:ENSG00000133398 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:6374326..6374350 26863196 MeRIP-seq:(Medium) rs775527943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1656172,Human_RBP_ID_15484811,Human_RBP_ID_19125284 Human_Splice_Rec_633560,Human_Splice_Rec_633561,Human_Splice_Rec_633563 56190 RMVar_ID_56190 Human_SNP_ID_220348147 m1A Human chr5 - 6374426 6374426 6374426 AGAATGCTAATTGAAATATATCGTGTTTCCAGATATATAGATCAAGGTCGAAATCCCCAGCTCTA AGAATGCTAATTGAAATATATCGTGTTTCCAGGTATATAGATCAAGGTCGAAATCCCCAGCTCTA T C MED10 Ensembl:ENSG00000133398 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:6374401..6374450 26863196 MeRIP-seq:(Medium) rs758388748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2942000,Human_RBP_ID_22680298 Human_Splice_Rec_633560 56191 RMVar_ID_56191 Human_SNP_ID_220349197 m1A Human chr5 + 6378471 6378471 6378471 GAACTTCTCCAGGTGCTCCTCTAGGTGGTCAAACTTCTCCGCCATCGCCTCGGCCCGTCCCCGAC GAACTTCTCCAGGTGCTCCTCTAGGTGGTCAAGCTTCTCCGCCATCGCCTCGGCCCGTCCCCGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:6377151..6378575 26863196 MeRIP-seq:(Medium) rs974797528 Functional Loss SNV dbSNP153 33..33 33 - - - 56192 RMVar_ID_56192 Human_SNP_ID_220409373 m1A Human chr5 - 6607312 6607312 6607312 TGAGCCCTGCAGATCTCACAGAAGGGAAACCCACAGATCCCTCTAAGCTGGAAAGTCCGTCATTC TGAGCCCTGCAGATCTCACAGAAGGGAAACCCGCAGATCCCTCTAAGCTGGAAAGTCCGTCATTC T C NSUN2 Ensembl:ENSG00000037474 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:6607146..6607354 26863196 MeRIP-seq:(Medium) rs1264552794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4836316,Human_RBP_ID_9398898,Human_RBP_ID_17530863 Human_Splice_Rec_633708,Human_Splice_Rec_633742,Human_Splice_Rec_633766,Human_Splice_Rec_633806 RMVar_hsa_circ_13898,RMVar_hsa_circ_119694,RMVar_hsa_circ_335043,RMVar_hsa_circ_378446,RMVar_hsa_circ_230089,RMVar_hsa_circ_370269,RMVar_hsa_circ_230091,RMVar_hsa_circ_230092,RMVar_hsa_circ_32759,RMVar_hsa_circ_300974,RMVar_hsa_circ_337533,RMVar_hsa_circ_333147,RMVar_hsa_circ_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096 56193 RMVar_ID_56193 Human_SNP_ID_220414338 m1A Human chr5 - 6624365 6624365 6624365 GATTAGGAGTCAGCGTGATGAGAGCTCTTGAGATGAATGGCAATAACCTCTGGGTTATGGAAAGC GATTAGGAGTCAGCGTGATGAGAGCTCTTGAGGTGAATGGCAATAACCTCTGGGTTATGGAAAGC T C NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:6624363..6624523 26863196 MeRIP-seq:(Medium) rs1055758924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838487,Human_RBP_ID_8620559,Human_RBP_ID_10217609,Human_RBP_ID_15497454 RMVar_hsa_circ_335043,RMVar_hsa_circ_230092,RMVar_hsa_circ_32759,RMVar_hsa_circ_300974,RMVar_hsa_circ_83064,RMVar_hsa_circ_230097,RMVar_hsa_circ_288256,RMVar_hsa_circ_338025,RMVar_hsa_circ_230101,RMVar_hsa_circ_113484,RMVar_hsa_circ_345729,RMVar_hsa_circ_82232,RMVar_hsa_circ_230105,RMVar_hsa_circ_278471,RMVar_hsa_circ_92683,RMVar_hsa_circ_230108,RMVar_hsa_circ_230109,RMVar_hsa_circ_230107,RMVar_hsa_circ_283647,RMVar_hsa_circ_377803,RMVar_hsa_circ_96691,RMVar_hsa_circ_230112,RMVar_hsa_circ_230113,RMVar_hsa_circ_230111 56194 RMVar_ID_56194 Human_SNP_ID_220416657 m1A Human chr5 + 6632702 6632702 6632702 GCCCTCGGGCACGATCTTGAGCTCCTGGTAGTAGTGCTCGAACAGCTTGTTCTCCTTGACGATCT GCCCTCGGGCACGATCTTGAGCTCCTGGTAGTTGTGCTCGAACAGCTTGTTCTCCTTGACGATCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:6632651..6632750 32194978 MeRIP-seq:(Medium) rs1293190085 Functional Loss SNV dbSNP153 33..33 33 - - - 56195 RMVar_ID_56195 Human_SNP_ID_220416820 m1A Human chr5 + 6632959 6632959 6632959 TCCTCCGGCCGCTGCTGTTGCTGGAGCCGCCGACCCCGCGACCGCCGCCCCATAGCCCACGCGGC TCCTCCGGCCGCTGCTGTTGCTGGAGCCGCCGGCCCCGCGACCGCCGCCCCATAGCCCACGCGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:6632741..6633050 26863196 MeRIP-seq:(Medium) rs184594943 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_152,Clinvar_Rec_153,Clinvar_Rec_154,Clinvar_Rec_155 GWAS_ID_6696,GWAS_ID_6697,GWAS_ID_6698,GWAS_ID_6699,GWAS_ID_6700,GWAS_ID_6701,GWAS_ID_6702,GWAS_ID_6703,GWAS_ID_6704,GWAS_ID_6705,GWAS_ID_6706,GWAS_ID_6707,GWAS_ID_6708,GWAS_ID_6709,GWAS_ID_6710,GWAS_ID_6711 56196 RMVar_ID_56196 Human_SNP_ID_220416841 m1A Human chr5 + 6633010 6633010 6633010 ATAGCCCACGCGGCCGCGCACGCAGCACGCAGAAACCGGCCCGCCACGGCCAGAACTCTAGCCCT ATAGCCCACGCGGCCGCGCACGCAGCACGCAGGAACCGGCCCGCCACGGCCAGAACTCTAGCCCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:6632901..6633050 26863196 MeRIP-seq:(Medium) rs1335100968 Functional Loss SNV dbSNP153 33..33 33 - - - 56197 RMVar_ID_56197 Human_SNP_ID_220416868 m1A Human chr5 - 6633042 6633042 6633042 CTTGGTTTCCGGCCGGAAGTCCCGGGAGGTGTAGGGCTAGAGTTCTGGCCGTGGCGGGCCGGTTT CTTGGTTTCCGGCCGGAAGTCCCGGGAGGTGTGGGGCTAGAGTTCTGGCCGTGGCGGGCCGGTTT T C NSUN2 Ensembl:ENSG00000037474 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:6632992..6633093 32194978 MeRIP-seq:(Medium) rs542676574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4836402,Human_RBP_ID_9306905,Human_RBP_ID_9335174,Human_RBP_ID_9354563,Human_RBP_ID_17157503,Human_RBP_ID_18424927 56198 RMVar_ID_56198 Human_SNP_ID_220417234 m1A Human chr5 - 6633854 6633854 6633854 GGGGCCGGGGACGTTACCGATGCCCGTAGTGGACGAGGAACATGGCCAGGAGGATGCAGTTGGGC GGGGCCGGGGACGTTACCGATGCCCGTAGTGGTCGAGGAACATGGCCAGGAGGATGCAGTTGGGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:6633744..6633925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 56199 RMVar_ID_56199 Human_SNP_ID_220417235 m1A Human chr5 - 6633854 6633854 6633854 GGGGCCGGGGACGTTACCGATGCCCGTAGTGGACGAGGAACATGGCCAGGAGGATGCAGTTGGGC GGGGCCGGGGACGTTACCGATGCCCGTAGTGGGCGAGGAACATGGCCAGGAGGATGCAGTTGGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:6633744..6633925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 56200 RMVar_ID_56200 Human_SNP_ID_220417273 m1A Human chr5 - 6633916 6633916 6633916 GGCACCGGGCAGTGAGGGGAGGGTCGGAGAGGACGCCGGGCCGGGAGTAGGGTAGGGGGCCGGGG GGCACCGGGCAGTGAGGGGAGGGTCGGAGAGGGCGCCGGGCCGGGAGTAGGGTAGGGGGCCGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:6633866..6633962 26863196 MeRIP-seq:(Medium) rs755501763 Functional Loss SNV dbSNP153 33..33 33 - - - 56201 RMVar_ID_56201 Human_SNP_ID_220436727 m1A Human chr5 + 6713711 6713711 6713711 CGCGCCGCGTGAAGCGGGAGCCCGGAGACCGCAGCCGCCCGCTGGGACGCGCCAAGCGCCGGAGC CGCGCCGCGTGAAGCGGGAGCCCGGAGACCGCCGCCGCCCGCTGGGACGCGCCAAGCGCCGGAGC A C TENT4A Ensembl:ENSG00000112941 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr5:6713495..6713797;chr5:6713631..6713813 26863196 MeRIP-seq:(Medium) rs1269704943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845135,Human_RBP_ID_9335176,Human_RBP_ID_19015527 56202 RMVar_ID_56202 Human_SNP_ID_220436849 m1A Human chr5 - 6713941 6713941 6713941 CCCCCGCGGGGCCCGCGCGCCCGCCCGCCCCGACGCGGCCCCGCCCCCGCCGCGCCCCGAGGCCC CCCCCGCGGGGCCCGCGCGCCCGCCCGCCCCGCCGCGGCCCCGCCCCCGCCGCGCCCCGAGGCCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:6713925..6714125 26863196 MeRIP-seq:(Medium) rs1460531451 Functional Loss SNV dbSNP153 33..33 33 - - - 56203 RMVar_ID_56203 Human_SNP_ID_220436984 m1A Human chr5 - 6714314 6714314 6714314 CGACTCCGCGTTGGACGAGGAGGACGACGACGAGGACGACAGCGACGGCGACTTGTGCAAGCGCC CGACTCCGCGTTGGACGAGGAGGACGACGACGTGGACGACAGCGACGGCGACTTGTGCAAGCGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:6714264..6714400 26863196 MeRIP-seq:(Medium) rs954915147 Functional Loss SNV dbSNP153 33..33 33 - - - 56204 RMVar_ID_56204 Human_SNP_ID_220444926 m1A Human chr5 - 6743299 6743299 6743299 GGCAGAGCGGCAGGAGATGGCAGGAGGGAGGGAAAGCCTGGCTGCTGCTGTTCGTGTTGCGCTTG GGCAGAGCGGCAGGAGATGGCAGGAGGGAGGGGAAGCCTGGCTGCTGCTGTTCGTGTTGCGCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:6743258..6743371 26863196 MeRIP-seq:(Medium) rs1216608834 Functional Loss SNV dbSNP153 33..33 33 - - - 56205 RMVar_ID_56205 Human_SNP_ID_220444950 m1A Human chr5 + 6743367 6743367 6743367 CTTGCCAGCCTCACTCTGCTCTCCTGCTCCGGAGGCCCCCACTGTCCTCATGGCCTGTGTAGCAA CTTGCCAGCCTCACTCTGCTCTCCTGCTCCGGGGGCCCCCACTGTCCTCATGGCCTGTGTAGCAA A G TENT4A Ensembl:ENSG00000112941 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:6743282..6743443 26863196 MeRIP-seq:(Medium) rs1258465515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21189462 RMVar_hsa_circ_282601,RMVar_hsa_circ_327568,RMVar_hsa_circ_340625,RMVar_hsa_circ_367450,RMVar_hsa_circ_230120,RMVar_hsa_circ_230119,RMVar_hsa_circ_40612,RMVar_hsa_circ_48680,RMVar_hsa_circ_370604 56206 RMVar_ID_56206 Human_SNP_ID_220446852 m1A Human chr5 - 6750476 6750476 6750476 CTTACAACGTCACTCCCAGAAAGTGAAGACACAGAAGAGGCCGAGGAGCCTGAAGACAGGAGCTG CTTACAACGTCACTCCCAGAAAGTGAAGACACGGAAGAGGCCGAGGAGCCTGAAGACAGGAGCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:6750426..6750500 32194978 MeRIP-seq:(Medium) rs1286710397 Functional Loss SNV dbSNP153 33..33 33 - - - 56207 RMVar_ID_56207 Human_SNP_ID_220447565 m1A Human chr5 - 6752978 6752978 6752978 CGGGTTGGGGGACGCTGAGGGAATGGCCGGGGAAGACATGTGGTGGACGGCTTTCAAAGACGCAG CGGGTTGGGGGACGCTGAGGGAATGGCCGGGGGAGACATGTGGTGGACGGCTTTCAAAGACGCAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:6752976..6753000 26863196 MeRIP-seq:(Medium) rs1801745 Functional Loss SNV dbSNP153 33..33 33 - - - 56208 RMVar_ID_56208 Human_SNP_ID_220453626 m1A Human chr5 + 6774397 6774397 6774397 GCTCCCCCACACACCCCGCCGCTCCCACACACACCCCCCGCCGCTCCCACACACACCCCCCGCCG GCTCCCCCACACACCCCGCCGCTCCCACACACCCCCCCCGCCGCTCCCACACACACCCCCCGCCG A C LINC02236 Ensembl:ENSG00000251365 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:6774349..6774442 26863196 MeRIP-seq:(Medium) rs1244243403 Functional Loss SNV dbSNP153 33..33 33 - - - 56209 RMVar_ID_56209 Human_SNP_ID_220725453 m1A Human chr5 - 7869217 7869217 7869217 GGAATCCGGGAACCGTAGCCGACAGGCAGCTTACCCACGCCGCGCCAGCCGGGCACGAACCTGCA GGAATCCGGGAACCGTAGCCGACAGGCAGCTTTCCCACGCCGCGCCAGCCGGGCACGAACCTGCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:7869189..7869263;chr5:7869189..7869273 26863196 MeRIP-seq:(Medium) rs1012740277 Functional Loss SNV dbSNP153 33..33 33 - - - 56210 RMVar_ID_56210 Human_SNP_ID_220731147 m1A Human chr5 - 7889185 7889185 7889185 GCAGGCACAGGCATCTCGTACAAAGCGGCTATAATCGGCTGCCCCTTGTTTACTGCACAGCTCCT GCAGGCACAGGCATCTCGTACAAAGCGGCTATGATCGGCTGCCCCTTGTTTACTGCACAGCTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:7889136..7889250 26863196 MeRIP-seq:(Medium) rs1268284059 Functional Loss SNV dbSNP153 33..33 33 - - - 56211 RMVar_ID_56211 Human_SNP_ID_220732197 m1A Human chr5 + 7892817 7892817 7892817 TCTACTGCCACAACAGAGGTTCTGCGGAAGGGAGTATGTACAGGCTGGCTGGCCTTGTTGGTTGC TCTACTGCCACAACAGAGGTTCTGCGGAAGGGCGTATGTACAGGCTGGCTGGCCTTGTTGGTTGC A C MTRR Ensembl:ENSG00000124275 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:7892782..7892863 32194978 MeRIP-seq:(Medium) rs1462412733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7474861,Human_RBP_ID_9397622,Human_RBP_ID_15525299,Human_RBP_ID_19014719,Human_RBP_ID_25932320,Human_RBP_ID_26350665 Human_Splice_Rec_634228,Human_Splice_Rec_634229,Human_Splice_Rec_634256,Human_Splice_Rec_634257,Human_Splice_Rec_634302,Human_Splice_Rec_634303,Human_Splice_Rec_634328,Human_Splice_Rec_634329,Human_Splice_Rec_634386,Human_Splice_Rec_634387,Human_Splice_Rec_634416,Human_Splice_Rec_634420,Human_Splice_Rec_634421,Human_Splice_Rec_634424 Human_miRNA_ID_1400397,Human_miRNA_ID_2397088,Human_miRNA_ID_2717181,Human_miRNA_ID_2729155 RMVar_hsa_circ_4352,RMVar_hsa_circ_88543,RMVar_hsa_circ_230155,RMVar_hsa_circ_336230,RMVar_hsa_circ_19286,RMVar_hsa_circ_269331,RMVar_hsa_circ_92604,RMVar_hsa_circ_230157,RMVar_hsa_circ_230158,RMVar_hsa_circ_90735 56212 RMVar_ID_56212 Human_SNP_ID_220874945 m1A Human chr5 + 8457761 8457761 8457761 CGCGCTGTCCATGGGCGTCCTTGGCCTGCGCCACCCAGGTGAGCGCTCCGGAGGCTGCGATCCCC CGCGCTGTCCATGGGCGTCCTTGGCCTGCGCCGCCCAGGTGAGCGCTCCGGAGGCTGCGATCCCC A G MIR4458HG Ensembl:ENSG00000247516 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:8457742..8457854 26863196 MeRIP-seq:(Medium) rs1231210769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845619,Human_RBP_ID_5612948,Human_RBP_ID_19125320 Human_Splice_Rec_634533,Human_Splice_Rec_634535,Human_Splice_Rec_634537,Human_Splice_Rec_634539,Human_Splice_Rec_634541,Human_Splice_Rec_634545 56213 RMVar_ID_56213 Human_SNP_ID_221149112 m1A Human chr5 - 9549095 9549095 9549095 CCCGGCTTTCCTTTGAAGGTCACTCATGGCCCACAGTCATGTCCTGATTTCTTCCAGGTGATGTT CCCGGCTTTCCTTTGAAGGTCACTCATGGCCCTCAGTCATGTCCTGATTTCTTCCAGGTGATGTT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:9549048..9549195 32194978 MeRIP-seq:(Medium) rs935373349 Functional Loss SNV dbSNP153 33..33 33 - - - 56214 RMVar_ID_56214 Human_SNP_ID_221315749 m1A Human chr5 - 10231450 10231450 10231450 ATGGGAAGGACACCAGCCCTTGGAAGGGCAGGAGCCTTGGGTGAGCAGAGAGGAATGCAGGGCTG ATGGGAAGGACACCAGCCCTTGGAAGGGCAGGGGCCTTGGGTGAGCAGAGAGGAATGCAGGGCTG T C ATPSCKMT Ensembl:ENSG00000150756 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:10230737..10231743 26863196 MeRIP-seq:(Medium) rs1248777995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7354947 RMVar_hsa_circ_128006,RMVar_hsa_circ_230199,RMVar_hsa_circ_230203 56215 RMVar_ID_56215 Human_SNP_ID_221315760 m1A Human chr5 - 10231501 10231501 10231501 AGCAGGCAGGTGTGGCATGAGTGTGCGTGGGGAGGTCAGAGAGGAAGCAGGATGGGAAGGACACC AGCAGGCAGGTGTGGCATGAGTGTGCGTGGGGGGGTCAGAGAGGAAGCAGGATGGGAAGGACACC T C ATPSCKMT Ensembl:ENSG00000150756 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:10231272..10231591;chr5:10230723..10231646 26863196 MeRIP-seq:(Medium) rs910224415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7354950,Human_RBP_ID_8213120 RMVar_hsa_circ_128006,RMVar_hsa_circ_230199,RMVar_hsa_circ_230203,RMVar_hsa_circ_230205 56216 RMVar_ID_56216 Human_SNP_ID_221321055 m1A Human chr5 - 10250351 10250351 10250351 GGCGCCCATATTCATCGAAGGCGAGGGTCCCCATGGACGCCATGGTGCAACAACCGGAATTACTT GGCGCCCATATTCATCGAAGGCGAGGGTCCCCGTGGACGCCATGGTGCAACAACCGGAATTACTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:10250301..10250410 26863196 MeRIP-seq:(Medium) rs1266043151 Functional Loss SNV dbSNP153 33..33 33 - - - 56217 RMVar_ID_56217 Human_SNP_ID_221322254 m1A Human chr5 - 10254204 10254204 10254204 TGCTAAAAAACACGGAATGGTGGACTCTTACCATTTGGTCCAAGTGATGTTCTCATTGTATTTGC TGCTAAAAAACACGGAATGGTGGACTCTTACCGTTTGGTCCAAGTGATGTTCTCATTGTATTTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:10254126..10254261 32194978 MeRIP-seq:(Medium) rs775126012 Functional Loss SNV dbSNP153 33..33 33 - - - 56218 RMVar_ID_56218 Human_SNP_ID_221324900 m1A Human chr5 - 10263134 10263134 10263134 CGCTCTCATGGCATACTGTTCTAAGGTGGGGCACTGGAAAGGTACAGAAGTATGGTGAGTGCACT CGCTCTCATGGCATACTGTTCTAAGGTGGGGCCCTGGAAAGGTACAGAAGTATGGTGAGTGCACT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:10263126..10263150 26863196 MeRIP-seq:(Medium) rs890262012 Functional Loss SNV dbSNP153 33..33 33 - - - 56219 RMVar_ID_56219 Human_SNP_ID_221324935 m1A Human chr5 - 10263228 10263228 10263228 CCTGTCTGGCTCGGACTTCGGTCATAGTCTGGATGGGATTCATGCCACTGTTTTCAGAGAGGGCC CCTGTCTGGCTCGGACTTCGGTCATAGTCTGGGTGGGATTCATGCCACTGTTTTCAGAGAGGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10263179..10263253 26863196 MeRIP-seq:(Medium) rs777140569 Functional Loss SNV dbSNP153 33..33 33 - - - 56220 RMVar_ID_56220 Human_SNP_ID_221325395 m1A Human chr5 + 10264617 10264617 10264617 TCAGAAAGAGTTGGTTATTGATAGTTTATTGTATGCTATTTTAGGATAATCAGTGTCCTTGTATT TCAGAAAGAGTTGGTTATTGATAGTTTATTGTGTGCTATTTTAGGATAATCAGTGTCCTTGTATT A G CCT5 Ensembl:ENSG00000150753 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10264615..10264758 26863196 MeRIP-seq:(Medium) rs747733119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100741,RMVar_hsa_circ_230209,RMVar_hsa_circ_106512,RMVar_hsa_circ_230210,RMVar_hsa_circ_112199,RMVar_hsa_circ_230212 56221 RMVar_ID_56221 Human_SNP_ID_221325437 m1A Human chr5 + 10264717 10264717 10264717 TTGATTGGCAAAAAGCAACAGATATCTCTTGCAACACAAATGGTTAGAATGATTTTGAAGATTGA TTGATTGGCAAAAAGCAACAGATATCTCTTGCGACACAAATGGTTAGAATGATTTTGAAGATTGA A G CCT5 Ensembl:ENSG00000150753 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs190090251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1642278,Human_RBP_ID_1982923,Human_RBP_ID_3751679,Human_RBP_ID_5610155,Human_RBP_ID_9397639,Human_RBP_ID_9444249,Human_RBP_ID_18828812,Human_RBP_ID_22459987,Human_RBP_ID_27329750 Human_Splice_Rec_634914,Human_Splice_Rec_634932,Human_Splice_Rec_634958,Human_Splice_Rec_635010,Human_Splice_Rec_635028,Human_Splice_Rec_635036 RMVar_hsa_circ_100741,RMVar_hsa_circ_230209,RMVar_hsa_circ_106512,RMVar_hsa_circ_230210,RMVar_hsa_circ_112199,RMVar_hsa_circ_230212 56222 RMVar_ID_56222 Human_SNP_ID_221329332 m1A Human chr5 - 10280522 10280522 10280522 GGGTTCGTGCATCGGAAGAGAGAAGATTGCTCACCTGCAGACAAGCCCTACATTGACGAGGCCAG GGGTTCGTGCATCGGAAGAGAGAAGATTGCTCTCCTGCAGACAAGCCCTACATTGACGAGGCCAG T A CMBL Ensembl:ENSG00000164237 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10280473..10280576 26863196 MeRIP-seq:(Medium) rs200019273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76393,Human_RBP_ID_788238,Human_RBP_ID_4847601,Human_RBP_ID_7356124,Human_RBP_ID_8597870 RMVar_hsa_circ_103527,RMVar_hsa_circ_230213 56223 RMVar_ID_56223 Human_SNP_ID_221331513 m1A Human chr5 - 10288529 10288527 10288530 AACTAAGATCAATTCATGTCCATATTTTGCAGAACCATTGTTCCAGACTTCTTTGTAGGGCAAGA AACTAAGATCAATTCATGTCCATATTTTGCA___CCATTGTTCCAGACTTCTTTGTAGGGCAAGA GTTC G CMBL Ensembl:ENSG00000164237 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10288490..10288561 26863196 MeRIP-seq:(Medium) rs1198505760 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_627589,Human_RBP_ID_25838159 Human_Splice_Rec_635042,Human_Splice_Rec_635052,Human_Splice_Rec_635060,Human_Splice_Rec_635066 RMVar_hsa_circ_72670,RMVar_hsa_circ_13836,RMVar_hsa_circ_330541 56224 RMVar_ID_56224 Human_SNP_ID_221349035 m1A Human chr5 - 10353572 10353572 10353572 GCACTGTCGGTCGGCGGCTAAGGAGGGGAGGCACCTGCATCTGGGGCGCGGCGAATCCTCGCGTG GCACTGTCGGTCGGCGGCTAAGGAGGGGAGGCGCCTGCATCTGGGGCGCGGCGAATCCTCGCGTG T C AC012640.4 Ensembl:ENSG00000259802 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10353268..10353584 26863196 MeRIP-seq:(Medium) rs1373047127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3784618,Human_RBP_ID_4802015 56225 RMVar_ID_56225 Human_SNP_ID_221349208 m1A Human chr5 + 10353878 10353878 10353878 CCGCCCGGCCGCGGGAGCCTCGTGGCTGCGTCACCGCCGCCCCCCCAGACAAGATGGACACCGCG CCGCCCGGCCGCGGGAGCCTCGTGGCTGCGTCTCCGCCGCCCCCCCAGACAAGATGGACACCGCG A T MARCHF6 Ensembl:ENSG00000145495 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:10353701..10353931 26863196 MeRIP-seq:(Medium) rs1323515810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75449,Human_RBP_ID_250137,Human_RBP_ID_627618,Human_RBP_ID_945617,Human_RBP_ID_18955867 Human_Splice_Rec_635073,Human_Splice_Rec_635123,Human_Splice_Rec_635171,Human_Splice_Rec_635179,Human_Splice_Rec_635227,Human_Splice_Rec_635271 Human_miRNA_ID_2386470,Human_miRNA_ID_2387943,Human_miRNA_ID_2399097,Human_miRNA_ID_3030149 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215 56226 RMVar_ID_56226 Human_SNP_ID_221350496 m1A Human chr5 + 10358061 10358061 10358061 GCGATCTTGGCTCACTAGGGGTCGCAGTTTTAAATATAGCAGTAAAGGAAGGCCTCACTGAGAAG GCGATCTTGGCTCACTAGGGGTCGCAGTTTTACATATAGCAGTAAAGGAAGGCCTCACTGAGAAG A C MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10358054..10358350 26863196 MeRIP-seq:(Medium) rs1290604996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15252327 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215 56227 RMVar_ID_56227 Human_SNP_ID_221350497 m1A Human chr5 + 10358061 10358061 10358061 GCGATCTTGGCTCACTAGGGGTCGCAGTTTTAAATATAGCAGTAAAGGAAGGCCTCACTGAGAAG GCGATCTTGGCTCACTAGGGGTCGCAGTTTTAGATATAGCAGTAAAGGAAGGCCTCACTGAGAAG A G MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10358054..10358350 26863196 MeRIP-seq:(Medium) rs1290604996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15252327 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215 56228 RMVar_ID_56228 Human_SNP_ID_221355256 m1A Human chr5 + 10376389 10376389 10376389 CCAGCGAGACCACGAACCCACCAGAAGGAAGAAACTCCGAACACGTCCGAACATCAGAAGGAACA CCAGCGAGACCACGAACCCACCAGAAGGAAGACACTCCGAACACGTCCGAACATCAGAAGGAACA A C MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:10376379..10376493 26863196 MeRIP-seq:(Medium) rs1184489588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 56229 RMVar_ID_56229 Human_SNP_ID_221359229 m1A Human chr5 + 10391657 10391655 10391658 AAACCCTGATGCCCAGGATGACCAGGCAGAAGAGGAGGAGGAGGACAATGAGGAGGAAGATGACG AAACCCTGATGCCCAGGATGACCAGGCAGAA___GAGGAGGAGGACAATGAGGAGGAAGATGACG AGAG A MARCHF6 Ensembl:ENSG00000145495 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:10391607..10391768 26863196 MeRIP-seq:(Medium) rs758962731 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_75471,Human_RBP_ID_3967777,Human_RBP_ID_5610164,Human_RBP_ID_7357127,Human_RBP_ID_15253754,Human_RBP_ID_19015546,Human_RBP_ID_21085517,Human_RBP_ID_22459114,Human_RBP_ID_22771335,Human_RBP_ID_23050093,Human_RBP_ID_23116238,Human_RBP_ID_26350674,Human_RBP_ID_27825249 Human_Splice_Rec_635085,Human_Splice_Rec_635133,Human_Splice_Rec_635191,Human_Splice_Rec_635233 Human_miRNA_ID_2254348 RMVar_hsa_circ_35462,RMVar_hsa_circ_230214,RMVar_hsa_circ_116223,RMVar_hsa_circ_317192,RMVar_hsa_circ_342281,RMVar_hsa_circ_370049,RMVar_hsa_circ_337058,RMVar_hsa_circ_52343,RMVar_hsa_circ_64370,RMVar_hsa_circ_14764,RMVar_hsa_circ_27674,RMVar_hsa_circ_230220,RMVar_hsa_circ_29769,RMVar_hsa_circ_230221,RMVar_hsa_circ_230219,RMVar_hsa_circ_326284,RMVar_hsa_circ_378915,RMVar_hsa_circ_322126,RMVar_hsa_circ_104324,RMVar_hsa_circ_48049,RMVar_hsa_circ_75415,RMVar_hsa_circ_322678,RMVar_hsa_circ_230226,RMVar_hsa_circ_22842,RMVar_hsa_circ_230225,RMVar_hsa_circ_361119,RMVar_hsa_circ_354683,RMVar_hsa_circ_267605,RMVar_hsa_circ_316152,RMVar_hsa_circ_267438,RMVar_hsa_circ_34647,RMVar_hsa_circ_73185,RMVar_hsa_circ_230229,RMVar_hsa_circ_276199,RMVar_hsa_circ_230227,RMVar_hsa_circ_230228,RMVar_hsa_circ_314797,RMVar_hsa_circ_334973,RMVar_hsa_circ_372884,RMVar_hsa_circ_299371,RMVar_hsa_circ_34200,RMVar_hsa_circ_42115,RMVar_hsa_circ_230231,RMVar_hsa_circ_230232,RMVar_hsa_circ_230230,RMVar_hsa_circ_10767,RMVar_hsa_circ_332796,RMVar_hsa_circ_367616,RMVar_hsa_circ_30903 56230 RMVar_ID_56230 Human_SNP_ID_221359238 m1A Human chr5 + 10391671 10391671 10391671 AGGATGACCAGGCAGAAGAGGAGGAGGAGGACAATGAGGAGGAAGATGACGCTGGTGTGGAGGAT AGGATGACCAGGCAGAAGAGGAGGAGGAGGACCATGAGGAGGAAGATGACGCTGGTGTGGAGGAT A C MARCHF6 Ensembl:ENSG00000145495 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10391551..10391750 26863196 MeRIP-seq:(Medium) rs767721638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75471,Human_RBP_ID_787950,Human_RBP_ID_839769,Human_RBP_ID_1983012,Human_RBP_ID_3967109,Human_RBP_ID_4802083,Human_RBP_ID_5610164,Human_RBP_ID_7357128,Human_RBP_ID_10232538,Human_RBP_ID_15253754,Human_RBP_ID_19014728,Human_RBP_ID_22459114,Human_RBP_ID_22771335,Human_RBP_ID_22826824,Human_RBP_ID_23035949,Human_RBP_ID_23116238,Human_RBP_ID_26350674,Human_RBP_ID_26519240,Human_RBP_ID_27825249 Human_Splice_Rec_635085,Human_Splice_Rec_635133,Human_Splice_Rec_635191,Human_Splice_Rec_635233 Human_miRNA_ID_2254348 RMVar_hsa_circ_35462,RMVar_hsa_circ_230214,RMVar_hsa_circ_116223,RMVar_hsa_circ_317192,RMVar_hsa_circ_342281,RMVar_hsa_circ_370049,RMVar_hsa_circ_337058,RMVar_hsa_circ_52343,RMVar_hsa_circ_64370,RMVar_hsa_circ_14764,RMVar_hsa_circ_27674,RMVar_hsa_circ_230220,RMVar_hsa_circ_29769,RMVar_hsa_circ_230221,RMVar_hsa_circ_230219,RMVar_hsa_circ_326284,RMVar_hsa_circ_378915,RMVar_hsa_circ_322126,RMVar_hsa_circ_104324,RMVar_hsa_circ_48049,RMVar_hsa_circ_75415,RMVar_hsa_circ_322678,RMVar_hsa_circ_230226,RMVar_hsa_circ_22842,RMVar_hsa_circ_230225,RMVar_hsa_circ_361119,RMVar_hsa_circ_354683,RMVar_hsa_circ_267605,RMVar_hsa_circ_316152,RMVar_hsa_circ_267438,RMVar_hsa_circ_34647,RMVar_hsa_circ_73185,RMVar_hsa_circ_230229,RMVar_hsa_circ_276199,RMVar_hsa_circ_230227,RMVar_hsa_circ_230228,RMVar_hsa_circ_314797,RMVar_hsa_circ_334973,RMVar_hsa_circ_372884,RMVar_hsa_circ_299371,RMVar_hsa_circ_34200,RMVar_hsa_circ_42115,RMVar_hsa_circ_230231,RMVar_hsa_circ_230232,RMVar_hsa_circ_230230,RMVar_hsa_circ_10767,RMVar_hsa_circ_332796,RMVar_hsa_circ_367616,RMVar_hsa_circ_30903 56231 RMVar_ID_56231 Human_SNP_ID_221359239 m1A Human chr5 + 10391671 10391671 10391671 AGGATGACCAGGCAGAAGAGGAGGAGGAGGACAATGAGGAGGAAGATGACGCTGGTGTGGAGGAT AGGATGACCAGGCAGAAGAGGAGGAGGAGGACGATGAGGAGGAAGATGACGCTGGTGTGGAGGAT A G MARCHF6 Ensembl:ENSG00000145495 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10391551..10391750 26863196 MeRIP-seq:(Medium) rs767721638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75471,Human_RBP_ID_787950,Human_RBP_ID_839769,Human_RBP_ID_1983012,Human_RBP_ID_3967109,Human_RBP_ID_4802083,Human_RBP_ID_5610164,Human_RBP_ID_7357128,Human_RBP_ID_10232538,Human_RBP_ID_15253754,Human_RBP_ID_19014728,Human_RBP_ID_22459114,Human_RBP_ID_22771335,Human_RBP_ID_22826824,Human_RBP_ID_23035949,Human_RBP_ID_23116238,Human_RBP_ID_26350674,Human_RBP_ID_26519240,Human_RBP_ID_27825249 Human_Splice_Rec_635085,Human_Splice_Rec_635133,Human_Splice_Rec_635191,Human_Splice_Rec_635233 Human_miRNA_ID_2254348 RMVar_hsa_circ_35462,RMVar_hsa_circ_230214,RMVar_hsa_circ_116223,RMVar_hsa_circ_317192,RMVar_hsa_circ_342281,RMVar_hsa_circ_370049,RMVar_hsa_circ_337058,RMVar_hsa_circ_52343,RMVar_hsa_circ_64370,RMVar_hsa_circ_14764,RMVar_hsa_circ_27674,RMVar_hsa_circ_230220,RMVar_hsa_circ_29769,RMVar_hsa_circ_230221,RMVar_hsa_circ_230219,RMVar_hsa_circ_326284,RMVar_hsa_circ_378915,RMVar_hsa_circ_322126,RMVar_hsa_circ_104324,RMVar_hsa_circ_48049,RMVar_hsa_circ_75415,RMVar_hsa_circ_322678,RMVar_hsa_circ_230226,RMVar_hsa_circ_22842,RMVar_hsa_circ_230225,RMVar_hsa_circ_361119,RMVar_hsa_circ_354683,RMVar_hsa_circ_267605,RMVar_hsa_circ_316152,RMVar_hsa_circ_267438,RMVar_hsa_circ_34647,RMVar_hsa_circ_73185,RMVar_hsa_circ_230229,RMVar_hsa_circ_276199,RMVar_hsa_circ_230227,RMVar_hsa_circ_230228,RMVar_hsa_circ_314797,RMVar_hsa_circ_334973,RMVar_hsa_circ_372884,RMVar_hsa_circ_299371,RMVar_hsa_circ_34200,RMVar_hsa_circ_42115,RMVar_hsa_circ_230231,RMVar_hsa_circ_230232,RMVar_hsa_circ_230230,RMVar_hsa_circ_10767,RMVar_hsa_circ_332796,RMVar_hsa_circ_367616,RMVar_hsa_circ_30903 56232 RMVar_ID_56232 Human_SNP_ID_221360536 m1A Human chr5 - 10396622 10396622 10396622 CCATGCTGACACTGACCAGACTGCCCAAGTCCATTCATTCATGCCCACAACCTTCCCCGCAACCA CCATGCTGACACTGACCAGACTGCCCAAGTCCCTTCATTCATGCCCACAACCTTCCCCGCAACCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:10396607..10396825 26863196 MeRIP-seq:(Medium) rs573615807 Functional Loss SNV dbSNP153 33..33 33 - - - 56233 RMVar_ID_56233 Human_SNP_ID_221364206 m1A Human chr5 - 10411452 10411452 10411452 CCTGCTGGAGTATGGCTTGGTGGGCTGCATGAAGGCCTTCTCCCACCACAGGAATAGCGTTGTTA CCTGCTGGAGTATGGCTTGGTGGGCTGCATGAGGGCCTTCTCCCACCACAGGAATAGCGTTGTTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:10411401..10411525 32194978 MeRIP-seq:(Medium) rs1228881545 Functional Loss SNV dbSNP153 33..33 33 - - - 56234 RMVar_ID_56234 Human_SNP_ID_221370037 m1A Human chr5 - 10435350 10435350 10435350 TTTCCAATTTTGCCTAGGTTGGCCTCGAACGCATAGCCTCGCCTCCTTGTGTGCCAGGACAACCG TTTCCAATTTTGCCTAGGTTGGCCTCGAACGCGTAGCCTCGCCTCCTTGTGTGCCAGGACAACCG T C ROPN1L-AS1 RNACentral:URS0000D5AEAC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10435301..10435405 26863196 MeRIP-seq:(Medium) rs1318060676 Functional Loss SNV dbSNP153 33..33 33 - - - 56235 RMVar_ID_56235 Human_SNP_ID_221423925 m1A Human chr5 - 10639203 10639178 10639204 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCGCCTAACATCGCCGCGCAACGCCGC CACGTCACCCGCTAACATCGCCGCGCAACTC__________________________AACGCCGC TGCGCGGCGATGTTAGGCGGTGACGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639196..10639261 26863196 MeRIP-seq:(Medium) rs1385082296 Functional Loss DEL dbSNP153 32..57 33 - - - 56236 RMVar_ID_56236 Human_SNP_ID_221423936 m1A Human chr5 - 10639203 10639203 10639203 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCGCCTAACATCGCCGCGCAACGCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCCGCGTCACCGCCTAACATCGCCGCGCAACGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639196..10639261 26863196 MeRIP-seq:(Medium) rs377046957 Functional Loss SNV dbSNP153 33..33 33 - - - 56237 RMVar_ID_56237 Human_SNP_ID_221424174 m1A Human chr5 - 10640009 10639823 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_________________________________ CGGAGTTGCGCGGCGATGTTAGCGGGTGACGCGGCGTTGCGCGGCGATGTTAGGCGGTGACGTGGAGTTGTGCGGCGATGTTAGCGGGTGACGTGGGGTTGCGCGGCGATGTTAGGCGGTGACGTGGAGTTGCGCGGTGATGTTAGCGGGTGACGCGGAGTTGCGCGGCGATGTTAGCGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs1560985258 Functional Loss DEL dbSNP153 33..65 33 - - - 56238 RMVar_ID_56238 Human_SNP_ID_221424199 m1A Human chr5 - 10640009 10639854 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_________________________________ CGGCGTTGCGCGGCGATGTTAGGCGGTGACGTGGAGTTGTGCGGCGATGTTAGCGGGTGACGTGGGGTTGCGCGGCGATGTTAGGCGGTGACGTGGAGTTGCGCGGTGATGTTAGCGGGTGACGCGGAGTTGCGCGGCGATGTTAGCGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs1560985293 Functional Loss DEL dbSNP153 33..65 33 - - - 56239 RMVar_ID_56239 Human_SNP_ID_221424237 m1A Human chr5 - 10640009 10639895 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_________________________________ CGGCGATGTTAGCGGGTGACGTGGGGTTGCGCGGCGATGTTAGGCGGTGACGTGGAGTTGCGCGGTGATGTTAGCGGGTGACGCGGAGTTGCGCGGCGATGTTAGCGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs1560985367 Functional Loss DEL dbSNP153 33..65 33 - - - 56240 RMVar_ID_56240 Human_SNP_ID_221424279 m1A Human chr5 - 10640009 10639955 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_________________________________ CGCGGTGATGTTAGCGGGTGACGCGGAGTTGCGCGGCGATGTTAGCGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs1560985444 Functional Loss DEL dbSNP153 33..65 33 - - - 56241 RMVar_ID_56241 Human_SNP_ID_221424295 m1A Human chr5 - 10640009 10639978 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_______________________________GC CGGAGTTGCGCGGCGATGTTAGCGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs1485641405 Functional Loss DEL dbSNP153 33..63 33 - - - 56242 RMVar_ID_56242 Human_SNP_ID_221424310 m1A Human chr5 - 10640009 10640000 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCC_________GCTAACATCGCCGCGCAACTCCGC CGGGTGACGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs199598687 Functional Loss DEL dbSNP153 33..41 33 - - - 56243 RMVar_ID_56243 Human_SNP_ID_221424324 m1A Human chr5 - 10640009 10640009 10640009 CACGTCACCCGCTAACATCGCCGCGCAACTCCACGTCACCCGCTAACATCGCCGCGCAACTCCGC CACGTCACCCGCTAACATCGCCGCGCAACTCCGCGTCACCCGCTAACATCGCCGCGCAACTCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10639959..10640054 26863196 MeRIP-seq:(Medium) rs111629567 Functional Loss SNV dbSNP153 33..33 33 - - - 56244 RMVar_ID_56244 Human_SNP_ID_221427217 m1A Human chr5 + 10650034 10650034 10650034 GCGGTACAAGGAGGCCAAGGAGGAGAAGAGGAAGGCAGAGGAGGCCGAAAAGAAGCGCCAGGCCG GCGGTACAAGGAGGCCAAGGAGGAGAAGAGGAGGGCAGAGGAGGCCGAAAAGAAGCGCCAGGCCG A G ANKRD33B Ensembl:ENSG00000164236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10649589..10650257 26863196 MeRIP-seq:(Medium) rs1560990401 Functional Loss SNV dbSNP153 33..33 33 - - - 56245 RMVar_ID_56245 Human_SNP_ID_221427232 m1A Human chr5 + 10650061 10650061 10650061 GAGGAAGGCAGAGGAGGCCGAAAAGAAGCGCCAGGCCGAGGCGCAGAAGGAGAGGCGCACTGCGC GAGGAAGGCAGAGGAGGCCGAAAAGAAGCGCCGGGCCGAGGCGCAGAAGGAGAGGCGCACTGCGC A G ANKRD33B Ensembl:ENSG00000164236 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10649820..10650180 26863196 MeRIP-seq:(Medium) rs1474831640 Functional Loss SNV dbSNP153 33..33 33 - - - 56246 RMVar_ID_56246 Human_SNP_ID_221432851 m1A Human chr5 + 10670247 10670247 10670247 TGATGATGGTGGTGATGGTGATGATGGTGGTGATGGTGGTGATGGTGGTGATGATGGTGATGATG TGATGATGGTGGTGATGGTGATGATGGTGGTGGTGGTGGTGATGGTGGTGATGATGGTGATGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10670223..10670294 26863196 MeRIP-seq:(Medium) rs1447173577 Functional Loss SNV dbSNP153 33..33 33 - - - 56247 RMVar_ID_56247 Human_SNP_ID_221435643 m1A Human chr5 - 10681031 10681031 10681031 GCAAGTGAGCCTGGAGTCCACCAGCCTGCCCCATGGCCCCGGCTCTGCTGCACTTGGTATTTCCC GCAAGTGAGCCTGGAGTCCACCAGCCTGCCCCTTGGCCCCGGCTCTGCTGCACTTGGTATTTCCC T A DAP Ensembl:ENSG00000112977 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10680980..10681116 26863196 MeRIP-seq:(Medium) rs1433526832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_627960,Human_RBP_ID_4802791,Human_RBP_ID_8214308,Human_RBP_ID_17301879,Human_RBP_ID_17415142,Human_RBP_ID_17662845,Human_RBP_ID_22614114 RMVar_hsa_circ_107577,RMVar_hsa_circ_230272 56248 RMVar_ID_56248 Human_SNP_ID_221435644 m1A Human chr5 - 10681031 10681031 10681031 GCAAGTGAGCCTGGAGTCCACCAGCCTGCCCCATGGCCCCGGCTCTGCTGCACTTGGTATTTCCC GCAAGTGAGCCTGGAGTCCACCAGCCTGCCCCGTGGCCCCGGCTCTGCTGCACTTGGTATTTCCC T C DAP Ensembl:ENSG00000112977 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10680980..10681116 26863196 MeRIP-seq:(Medium) rs1433526832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_627960,Human_RBP_ID_4802791,Human_RBP_ID_8214308,Human_RBP_ID_17301879,Human_RBP_ID_17415142,Human_RBP_ID_17662845,Human_RBP_ID_22614114 RMVar_hsa_circ_107577,RMVar_hsa_circ_230272 56249 RMVar_ID_56249 Human_SNP_ID_221435649 m1A Human chr5 - 10681044 10681044 10681044 ATCCAGCAGCCACGCAAGTGAGCCTGGAGTCCACCAGCCTGCCCCATGGCCCCGGCTCTGCTGCA ATCCAGCAGCCACGCAAGTGAGCCTGGAGTCCCCCAGCCTGCCCCATGGCCCCGGCTCTGCTGCA T G DAP Ensembl:ENSG00000112977 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:10680958..10683132 32194978 MeRIP-seq:(Medium) rs753757154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_627960,Human_RBP_ID_8214308,Human_RBP_ID_9397641,Human_RBP_ID_17303314,Human_RBP_ID_17415142,Human_RBP_ID_17662845 Human_miRNA_ID_2050898 RMVar_hsa_circ_107577,RMVar_hsa_circ_230272 56250 RMVar_ID_56250 Human_SNP_ID_221456398 m1A Human chr5 + 10761067 10761067 10761067 TAGTCTCTAGTTTCCCTTCGGGAGGCGAAGACATGACGCGGCGGGGCTTCCGCGGGGCCGAGGCG TAGTCTCTAGTTTCCCTTCGGGAGGCGAAGACGTGACGCGGCGGGGCTTCCGCGGGGCCGAGGCG A G AC012629.2 Ensembl:ENSG00000272324 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:10748176..10761275 26863196 MeRIP-seq:(Medium) rs1287408035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_635459 56251 RMVar_ID_56251 Human_SNP_ID_221456399 m1A Human chr5 - 10761068 10761068 10761068 CCGCCTCGGCCCCGCGGAAGCCCCGCCGCGTCATGTCTTCGCCTCCCGAAGGGAAACTAGAGACT CCGCCTCGGCCCCGCGGAAGCCCCGCCGCGTCCTGTCTTCGCCTCCCGAAGGGAAACTAGAGACT T G DAP Ensembl:ENSG00000112977 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10748131..10761275 26863196 MeRIP-seq:(Medium) rs1242688340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4803019,Human_RBP_ID_9335612,Human_RBP_ID_17415145,Human_RBP_ID_18829489 Human_Splice_Rec_635433,Human_Splice_Rec_635439,Human_Splice_Rec_635443,Human_Splice_Rec_635449,Human_Splice_Rec_635453,Human_Splice_Rec_635457 Human_miRNA_ID_2480581,Human_miRNA_ID_2951468 RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 56252 RMVar_ID_56252 Human_SNP_ID_221456400 m1A Human chr5 + 10761070 10761069 10761071 TCTCTAGTTTCCCTTCGGGAGGCGAAGACATGACGCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG TCTCTAGTTTCCCTTCGGGAGGCGAAGACATG__GCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG GAC G AC012629.2 Ensembl:ENSG00000272324 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:10748226..10761275 26863196 MeRIP-seq:(Medium) rs1363182855 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_635459 56253 RMVar_ID_56253 Human_SNP_ID_221456401 m1A Human chr5 + 10761070 10761070 10761070 TCTCTAGTTTCCCTTCGGGAGGCGAAGACATGACGCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG TCTCTAGTTTCCCTTCGGGAGGCGAAGACATGGCGCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG A G AC012629.2 Ensembl:ENSG00000272324 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:10748226..10761275 26863196 MeRIP-seq:(Medium) rs267927 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_635459 56254 RMVar_ID_56254 Human_SNP_ID_221456445 m1A Human chr5 + 10761143 10761143 10761143 CTCGGGCCGGGCGGGCGTGCGCGAGTGAGCTCAGGTGTGAGCGCCGGGGAGCGAGCGGGCGGGAG CTCGGGCCGGGCGGGCGTGCGCGAGTGAGCTCGGGTGTGAGCGCCGGGGAGCGAGCGGGCGGGAG A G AC012629.2 Ensembl:ENSG00000272324 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:10761060..10761223 26863410 MeRIP-seq:(Medium) rs984060894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_635459 56255 RMVar_ID_56255 Human_SNP_ID_222319840 m1A Human chr5 - 14143396 14143396 14143396 AGTCGCGAGGGCGGGGGCCCGTGGCCGGCGAGACCTCCGGGATCACGGGCGCCGGCGGCTGCCGC AGTCGCGAGGGCGGGGGCCCGTGGCCGGCGAGCCCTCCGGGATCACGGGCGCCGGCGGCTGCCGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:14143301..14143563 26863196 MeRIP-seq:(Medium) rs1016730545 Functional Loss SNV dbSNP153 33..33 33 - - - 56256 RMVar_ID_56256 Human_SNP_ID_222319841 m1A Human chr5 - 14143398 14143398 14143398 GCAGTCGCGAGGGCGGGGGCCCGTGGCCGGCGAGACCTCCGGGATCACGGGCGCCGGCGGCTGCC GCAGTCGCGAGGGCGGGGGCCCGTGGCCGGCGTGACCTCCGGGATCACGGGCGCCGGCGGCTGCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14143301..14143497 26863196 MeRIP-seq:(Medium) rs1356667243 Functional Loss SNV dbSNP153 33..33 33 - - - 56257 RMVar_ID_56257 Human_SNP_ID_222319896 m1A Human chr5 - 14143536 14143534 14143536 GGCTCGGCCCAAGGAGCGCGCCCACATAGACGAGGACTCCGCCCGGTAGCCGCGAGCTGGCCGAG GGCTCGGCCCAAGGAGCGCGCCCACATAGACG__GACTCCGCCCGGTAGCCGCGAGCTGGCCGAG CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:14143294..14143548 26863196 MeRIP-seq:(Medium) rs1237672501 Functional Loss DEL dbSNP153 33..34 33 - - - 56258 RMVar_ID_56258 Human_SNP_ID_222320434 m1A Human chr5 - 14145055 14145055 14145055 TCCCCAGCCCGGCCGTCCTCCCCGAGGCCGCCACCAGCACCCCCGCCCGCCTCTCCAGGCCCGGA TCCCCAGCCCGGCCGTCCTCCCCGAGGCCGCCCCCAGCACCCCCGCCCGCCTCTCCAGGCCCGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14144508..14145222 26863196 MeRIP-seq:(Medium) rs966721120 Functional Loss SNV dbSNP153 33..33 33 - - - 56259 RMVar_ID_56259 Human_SNP_ID_222337321 m1A Human chr5 + 14210041 14210041 14210041 CCAAGTGGGGTCCTGGTGCCGTGGGAGCCCTGATTGCTGGAGGAGCCCAGCTGGGGCCACAACTA CCAAGTGGGGTCCTGGTGCCGTGGGAGCCCTGGTTGCTGGAGGAGCCCAGCTGGGGCCACAACTA A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14210024..14210212 26863196 MeRIP-seq:(Medium) rs373757608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17158099 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 56260 RMVar_ID_56260 Human_SNP_ID_222337346 m1A Human chr5 + 14210124 14210124 14210124 ATGGCGCCCCAGGTGGGGTCAGGGGGAGTCAGATGGAGGAGCGGTCGGCCCCTTTGGTTGAGTTT ATGGCGCCCCAGGTGGGGTCAGGGGGAGTCAGTTGGAGGAGCGGTCGGCCCCTTTGGTTGAGTTT A T TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:14210113..14210189 26863196 MeRIP-seq:(Medium) rs1193416896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7397349,Human_RBP_ID_17159444 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 56261 RMVar_ID_56261 Human_SNP_ID_222361199 m1A Human chr5 + 14303309 14303309 14303309 TGGAGGGTGGCAGTGGAGGAGATTGAGCCGGGATTGGGATGGCTGCCACAGGAATTGATGATCCT TGGAGGGTGGCAGTGGAGGAGATTGAGCCGGGGTTGGGATGGCTGCCACAGGAATTGATGATCCT A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14303117..14303681 26863196 MeRIP-seq:(Medium) rs2697664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7398582 RMVar_hsa_circ_283,RMVar_hsa_circ_79613,RMVar_hsa_circ_230323,RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_323713,RMVar_hsa_circ_341444,RMVar_hsa_circ_347025,RMVar_hsa_circ_344313,RMVar_hsa_circ_324581,RMVar_hsa_circ_315318,RMVar_hsa_circ_122686,RMVar_hsa_circ_230329,RMVar_hsa_circ_230331,RMVar_hsa_circ_230333,RMVar_hsa_circ_72119,RMVar_hsa_circ_230334,RMVar_hsa_circ_230332,RMVar_hsa_circ_230330,RMVar_hsa_circ_230328,RMVar_hsa_circ_296611,RMVar_hsa_circ_64523,RMVar_hsa_circ_372445,RMVar_hsa_circ_323300,RMVar_hsa_circ_300557,RMVar_hsa_circ_48236,RMVar_hsa_circ_230336,RMVar_hsa_circ_230337,RMVar_hsa_circ_230335,RMVar_hsa_circ_371911,RMVar_hsa_circ_298615,RMVar_hsa_circ_119805,RMVar_hsa_circ_288034,RMVar_hsa_circ_104964,RMVar_hsa_circ_51064,RMVar_hsa_circ_25150,RMVar_hsa_circ_230341,RMVar_hsa_circ_230343,RMVar_hsa_circ_230345,RMVar_hsa_circ_230346,RMVar_hsa_circ_230344,RMVar_hsa_circ_230342,RMVar_hsa_circ_279668,RMVar_hsa_circ_290370,RMVar_hsa_circ_321654,RMVar_hsa_circ_322157,RMVar_hsa_circ_354676,RMVar_hsa_circ_297245,RMVar_hsa_circ_284160,RMVar_hsa_circ_48759,RMVar_hsa_circ_87690,RMVar_hsa_circ_42825,RMVar_hsa_circ_230348,RMVar_hsa_circ_5235,RMVar_hsa_circ_21682,RMVar_hsa_circ_230350,RMVar_hsa_circ_230351,RMVar_hsa_circ_230352,RMVar_hsa_circ_230349,RMVar_hsa_circ_276760,RMVar_hsa_circ_278990,RMVar_hsa_circ_323820,RMVar_hsa_circ_230347,RMVar_hsa_circ_312441,RMVar_hsa_circ_278308,RMVar_hsa_circ_74090,RMVar_hsa_circ_267896,RMVar_hsa_circ_12129,RMVar_hsa_circ_10233,RMVar_hsa_circ_230353,RMVar_hsa_circ_230355,RMVar_hsa_circ_230356,RMVar_hsa_circ_230354,RMVar_hsa_circ_270084,RMVar_hsa_circ_286703,RMVar_hsa_circ_341584,RMVar_hsa_circ_279310,RMVar_hsa_circ_117594,RMVar_hsa_circ_230357,RMVar_hsa_circ_230359,RMVar_hsa_circ_230360,RMVar_hsa_circ_230358 56262 RMVar_ID_56262 Human_SNP_ID_222371327 m1A Human chr5 - 14342070 14342067 14342070 TGCAGAGCTGAGCAATGGTCCCAGCACAAAGAAGACTGGATGCTCAATTGTTAGGCATAAAGACA TGCAGAGCTGAGCAATGGTCCCAGCACAAAGA___CTGGATGCTCAATTGTTAGGCATAAAGACA GTCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:14342068..14342177 32194978 MeRIP-seq:(Medium) rs1159571575 Functional Loss DEL dbSNP153 33..35 33 - - - 56263 RMVar_ID_56263 Human_SNP_ID_222381316 m1A Human chr5 + 14378054 14378054 14378054 TGAACTCTTCCAACGGGAGAACAGGGTATTGCATTACTGGACCATGAGGAAGAGACGGCTGGACC TGAACTCTTCCAACGGGAGAACAGGGTATTGCGTTACTGGACCATGAGGAAGAGACGGCTGGACC A G TRIO Ensembl:ENSG00000038382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:14374335..14387346 32194978 MeRIP-seq:(Medium) rs1415148491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73327,Human_RBP_ID_4850994,Human_RBP_ID_5617154,Human_RBP_ID_8885783,Human_RBP_ID_19014757 Human_Splice_Rec_636056,Human_Splice_Rec_636057,Human_Splice_Rec_636182,Human_Splice_Rec_636183,Human_Splice_Rec_636294,Human_Splice_Rec_636295,Human_Splice_Rec_636348,Human_Splice_Rec_636349,Human_Splice_Rec_636446,Human_Splice_Rec_636447 Human_miRNA_ID_2997931 RMVar_hsa_circ_283,RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_323713,RMVar_hsa_circ_344313,RMVar_hsa_circ_230333,RMVar_hsa_circ_72119,RMVar_hsa_circ_230334,RMVar_hsa_circ_372445,RMVar_hsa_circ_230335,RMVar_hsa_circ_371911,RMVar_hsa_circ_104964,RMVar_hsa_circ_230345,RMVar_hsa_circ_230346,RMVar_hsa_circ_321654,RMVar_hsa_circ_322157,RMVar_hsa_circ_297245,RMVar_hsa_circ_48759,RMVar_hsa_circ_42825,RMVar_hsa_circ_230348,RMVar_hsa_circ_5235,RMVar_hsa_circ_21682,RMVar_hsa_circ_230347,RMVar_hsa_circ_267896,RMVar_hsa_circ_12129,RMVar_hsa_circ_117594,RMVar_hsa_circ_230360,RMVar_hsa_circ_327306,RMVar_hsa_circ_127203,RMVar_hsa_circ_117880,RMVar_hsa_circ_97327,RMVar_hsa_circ_81706,RMVar_hsa_circ_95836,RMVar_hsa_circ_230361,RMVar_hsa_circ_230363,RMVar_hsa_circ_230362,RMVar_hsa_circ_117747,RMVar_hsa_circ_290455,RMVar_hsa_circ_283487,RMVar_hsa_circ_123830,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_92081,RMVar_hsa_circ_87477,RMVar_hsa_circ_65439,RMVar_hsa_circ_12918,RMVar_hsa_circ_10160,RMVar_hsa_circ_6539,RMVar_hsa_circ_725,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230376,RMVar_hsa_circ_230378,RMVar_hsa_circ_230377,RMVar_hsa_circ_230374,RMVar_hsa_circ_230375,RMVar_hsa_circ_230373,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_374000,RMVar_hsa_circ_124663,RMVar_hsa_circ_60142,RMVar_hsa_circ_230390,RMVar_hsa_circ_94977,RMVar_hsa_circ_230387,RMVar_hsa_circ_230385,RMVar_hsa_circ_230386,RMVar_hsa_circ_230384,RMVar_hsa_circ_102885,RMVar_hsa_circ_371972,RMVar_hsa_circ_374104,RMVar_hsa_circ_344072,RMVar_hsa_circ_309426,RMVar_hsa_circ_230388,RMVar_hsa_circ_230389,RMVar_hsa_circ_77854,RMVar_hsa_circ_376395,RMVar_hsa_circ_305427,RMVar_hsa_circ_230394,RMVar_hsa_circ_230395,RMVar_hsa_circ_343021,RMVar_hsa_circ_274753,RMVar_hsa_circ_54021,RMVar_hsa_circ_29201,RMVar_hsa_circ_37471,RMVar_hsa_circ_26772,RMVar_hsa_circ_7035,RMVar_hsa_circ_76844,RMVar_hsa_circ_126035,RMVar_hsa_circ_230397,RMVar_hsa_circ_5198,RMVar_hsa_circ_230398,RMVar_hsa_circ_3122,RMVar_hsa_circ_230400,RMVar_hsa_circ_97857,RMVar_hsa_circ_230399,RMVar_hsa_circ_79133,RMVar_hsa_circ_88005,RMVar_hsa_circ_230401,RMVar_hsa_circ_2594,RMVar_hsa_circ_230402,RMVar_hsa_circ_230403,RMVar_hsa_circ_350808,RMVar_hsa_circ_368633,RMVar_hsa_circ_92629,RMVar_hsa_circ_9948,RMVar_hsa_circ_60953,RMVar_hsa_circ_230406,RMVar_hsa_circ_6217,RMVar_hsa_circ_230405,RMVar_hsa_circ_230407 56264 RMVar_ID_56264 Human_SNP_ID_222383564 m1A Human chr5 + 14386171 14386171 14386171 TTTAAGGGGGTCCAGGGAGGGCCCGCTAAGAGAGTGGCGTTTATTTGAGTAGAGACATGAAGGAG TTTAAGGGGGTCCAGGGAGGGCCCGCTAAGAGGGTGGCGTTTATTTGAGTAGAGACATGAAGGAG A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:14386166..14386340 26863196 MeRIP-seq:(Medium) rs1212662494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283,RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_323713,RMVar_hsa_circ_344313,RMVar_hsa_circ_230333,RMVar_hsa_circ_72119,RMVar_hsa_circ_230334,RMVar_hsa_circ_372445,RMVar_hsa_circ_230335,RMVar_hsa_circ_104964,RMVar_hsa_circ_230346,RMVar_hsa_circ_321654,RMVar_hsa_circ_322157,RMVar_hsa_circ_48759,RMVar_hsa_circ_42825,RMVar_hsa_circ_5235,RMVar_hsa_circ_230347,RMVar_hsa_circ_12129,RMVar_hsa_circ_327306,RMVar_hsa_circ_127203,RMVar_hsa_circ_117880,RMVar_hsa_circ_97327,RMVar_hsa_circ_81706,RMVar_hsa_circ_95836,RMVar_hsa_circ_230361,RMVar_hsa_circ_230363,RMVar_hsa_circ_230362,RMVar_hsa_circ_117747,RMVar_hsa_circ_290455,RMVar_hsa_circ_283487,RMVar_hsa_circ_123830,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_92081,RMVar_hsa_circ_65439,RMVar_hsa_circ_12918,RMVar_hsa_circ_6539,RMVar_hsa_circ_725,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230376,RMVar_hsa_circ_230374,RMVar_hsa_circ_230375,RMVar_hsa_circ_230373,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_124663,RMVar_hsa_circ_60142,RMVar_hsa_circ_94977,RMVar_hsa_circ_230387,RMVar_hsa_circ_230385,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_374104,RMVar_hsa_circ_309426,RMVar_hsa_circ_230388,RMVar_hsa_circ_230389,RMVar_hsa_circ_376395,RMVar_hsa_circ_305427,RMVar_hsa_circ_230395,RMVar_hsa_circ_54021,RMVar_hsa_circ_29201,RMVar_hsa_circ_37471,RMVar_hsa_circ_26772,RMVar_hsa_circ_7035,RMVar_hsa_circ_76844,RMVar_hsa_circ_126035,RMVar_hsa_circ_5198,RMVar_hsa_circ_230398,RMVar_hsa_circ_3122,RMVar_hsa_circ_230400,RMVar_hsa_circ_97857,RMVar_hsa_circ_230399,RMVar_hsa_circ_79133,RMVar_hsa_circ_88005,RMVar_hsa_circ_230401,RMVar_hsa_circ_2594,RMVar_hsa_circ_230402,RMVar_hsa_circ_230403,RMVar_hsa_circ_92629,RMVar_hsa_circ_9948,RMVar_hsa_circ_230405,RMVar_hsa_circ_230410,RMVar_hsa_circ_371387,RMVar_hsa_circ_85947,RMVar_hsa_circ_230409 56265 RMVar_ID_56265 Human_SNP_ID_222388078 m1A Human chr5 - 14403082 14403001 14403083 TCACAACCTATGCCCTCACCACCACAACCTGTACCCTCACCACAACCTGCACCCTCACAACCCAC TCACAACCTATGCCCTCACCACCACAACCTG__________________________________ GCAGGTTGTGGTGAGGGTACAGGTTGTGGTGGTGAAGGTGCAGGTTGTGGTGGGTTGTGAGGGTGCAGGTTGTGGTGAGGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14402439..14403299 26863196 MeRIP-seq:(Medium) rs1561446627 Functional Loss DEL dbSNP153 32..65 33 - - - 56266 RMVar_ID_56266 Human_SNP_ID_222388123 m1A Human chr5 - 14403082 14403065 14403083 TCACAACCTATGCCCTCACCACCACAACCTGTACCCTCACCACAACCTGCACCCTCACAACCCAC TCACAACCTATGCCCTCACCACCACAACCTG__________________CACCCTCACAACCCAC GCAGGTTGTGGTGAGGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14402439..14403299 26863196 MeRIP-seq:(Medium) rs1450682979 Functional Loss DEL dbSNP153 32..49 33 - - - 56267 RMVar_ID_56267 Human_SNP_ID_222388335 m1A Human chr5 - 14403365 14403354 14403366 CCTACACCCTCACAACCTACACCCTCACCACAACCTGCACCCTCACAAGCTGCACCCTCACCACA CCTACACCCTCACAACCTACACCCTCACCAC____________CACAAGCTGCACCCTCACCACA GAGGGTGCAGGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14403352..14403734 26863196 MeRIP-seq:(Medium) rs1370921950 Functional Loss DEL dbSNP153 32..43 33 - - - 56268 RMVar_ID_56268 Human_SNP_ID_222388732 m1A Human chr5 - 14403923 14403920 14403923 ACACCCTCACAACCTGCACCCTCACCACCACCACCTACACCCTCACCACCACCACCTGCACCCTC ACACCCTCACAACCTGCACCCTCACCACCACC___TACACCCTCACCACCACCACCTGCACCCTC AGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14403903..14404231 26863196 MeRIP-seq:(Medium) rs1462801059 Functional Loss DEL dbSNP153 33..35 33 - - - 56269 RMVar_ID_56269 Human_SNP_ID_222388733 m1A Human chr5 - 14403923 14403923 14403923 ACACCCTCACAACCTGCACCCTCACCACCACCACCTACACCCTCACCACCACCACCTGCACCCTC ACACCCTCACAACCTGCACCCTCACCACCACCGCCTACACCCTCACCACCACCACCTGCACCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14403903..14404231 26863196 MeRIP-seq:(Medium) rs1168184538 Functional Loss SNV dbSNP153 33..33 33 - - - 56270 RMVar_ID_56270 Human_SNP_ID_222411798 m1A Human chr5 - 14487755 14487755 14487755 GGCCGGCCTCGGGGGCCGCGCCAGGGGGAGGCAGGGAGGGCCCGGGGGTGGACGTACCTGACATC GGCCGGCCTCGGGGGCCGCGCCAGGGGGAGGCGGGGAGGGCCCGGGGGTGGACGTACCTGACATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:14487581..14487856 26863196 MeRIP-seq:(Medium) rs1168379940 Functional Loss SNV dbSNP153 33..33 33 - - - 56271 RMVar_ID_56271 Human_SNP_ID_222411801 m1A Human chr5 - 14487759 14487759 14487759 CTGGGGCCGGCCTCGGGGGCCGCGCCAGGGGGAGGCAGGGAGGGCCCGGGGGTGGACGTACCTGA CTGGGGCCGGCCTCGGGGGCCGCGCCAGGGGGTGGCAGGGAGGGCCCGGGGGTGGACGTACCTGA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14487586..14487805 26863196 MeRIP-seq:(Medium) rs762813571 Functional Loss SNV dbSNP153 33..33 33 - - - 56272 RMVar_ID_56272 Human_SNP_ID_222411802 m1A Human chr5 - 14487759 14487759 14487759 CTGGGGCCGGCCTCGGGGGCCGCGCCAGGGGGAGGCAGGGAGGGCCCGGGGGTGGACGTACCTGA CTGGGGCCGGCCTCGGGGGCCGCGCCAGGGGGGGGCAGGGAGGGCCCGGGGGTGGACGTACCTGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14487586..14487805 26863196 MeRIP-seq:(Medium) rs762813571 Functional Loss SNV dbSNP153 33..33 33 - - - 56273 RMVar_ID_56273 Human_SNP_ID_222412014 m1A Human chr5 + 14488015 14488015 14488015 GGGCCGCTTCGCCGCTGAACTCGCCGCTCTCCAGCGCGGTCCCTTCTCTCGGCAAGGAGCCCTTC GGGCCGCTTCGCCGCTGAACTCGCCGCTCTCCGGCGCGGTCCCTTCTCTCGGCAAGGAGCCCTTC A G TRIO Ensembl:ENSG00000038382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:14487965..14488116 32194978 MeRIP-seq:(Medium) rs1162280967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8885835,Human_RBP_ID_9398967,Human_RBP_ID_19125370 RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_5235,RMVar_hsa_circ_117747,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_230387,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_7035,RMVar_hsa_circ_88005,RMVar_hsa_circ_230403,RMVar_hsa_circ_230410,RMVar_hsa_circ_85947,RMVar_hsa_circ_103203,RMVar_hsa_circ_230418,RMVar_hsa_circ_86070,RMVar_hsa_circ_6855,RMVar_hsa_circ_230423,RMVar_hsa_circ_79898,RMVar_hsa_circ_230428,RMVar_hsa_circ_113517,RMVar_hsa_circ_40021,RMVar_hsa_circ_100131,RMVar_hsa_circ_230430,RMVar_hsa_circ_230431,RMVar_hsa_circ_27394,RMVar_hsa_circ_107650,RMVar_hsa_circ_102966,RMVar_hsa_circ_123210,RMVar_hsa_circ_30472,RMVar_hsa_circ_230434,RMVar_hsa_circ_230435,RMVar_hsa_circ_84060,RMVar_hsa_circ_313382,RMVar_hsa_circ_230436,RMVar_hsa_circ_372177,RMVar_hsa_circ_230437,RMVar_hsa_circ_230438,RMVar_hsa_circ_35763,RMVar_hsa_circ_230439,RMVar_hsa_circ_347565 56274 RMVar_ID_56274 Human_SNP_ID_222412072 m1A Human chr5 + 14488070 14488070 14488070 GGAGCCCTTCCCCCCCAGCAGCCCCCTGCAGAAGGGGGGCTCCTTCTGGAGCTCCATCCCCGCCT GGAGCCCTTCCCCCCCAGCAGCCCCCTGCAGATGGGGGGCTCCTTCTGGAGCTCCATCCCCGCCT A T TRIO Ensembl:ENSG00000038382 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:14488026..14488200 26863196 MeRIP-seq:(Medium) rs759112471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_5235,RMVar_hsa_circ_117747,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_230387,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_7035,RMVar_hsa_circ_88005,RMVar_hsa_circ_230403,RMVar_hsa_circ_230410,RMVar_hsa_circ_85947,RMVar_hsa_circ_103203,RMVar_hsa_circ_230418,RMVar_hsa_circ_86070,RMVar_hsa_circ_6855,RMVar_hsa_circ_230423,RMVar_hsa_circ_79898,RMVar_hsa_circ_230428,RMVar_hsa_circ_113517,RMVar_hsa_circ_40021,RMVar_hsa_circ_100131,RMVar_hsa_circ_230430,RMVar_hsa_circ_230431,RMVar_hsa_circ_27394,RMVar_hsa_circ_107650,RMVar_hsa_circ_102966,RMVar_hsa_circ_123210,RMVar_hsa_circ_30472,RMVar_hsa_circ_230434,RMVar_hsa_circ_230435,RMVar_hsa_circ_84060,RMVar_hsa_circ_313382,RMVar_hsa_circ_230436,RMVar_hsa_circ_372177,RMVar_hsa_circ_230437,RMVar_hsa_circ_230438,RMVar_hsa_circ_35763,RMVar_hsa_circ_230439,RMVar_hsa_circ_347565 56275 RMVar_ID_56275 Human_SNP_ID_222412097 m1A Human chr5 - 14488094 14488094 14488094 AGGAGCCGGGTCGGCTGGCGGGGGAGGCGGGGATGGAGCTCCAGAAGGAGCCCCCCTTCTGCAGG AGGAGCCGGGTCGGCTGGCGGGGGAGGCGGGGGTGGAGCTCCAGAAGGAGCCCCCCTTCTGCAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14488051..14488175 26863196 MeRIP-seq:(Medium) rs772904946 Functional Loss SNV dbSNP153 33..33 33 - - - 56276 RMVar_ID_56276 Human_SNP_ID_222412098 m1A Human chr5 - 14488094 14488094 14488094 AGGAGCCGGGTCGGCTGGCGGGGGAGGCGGGGATGGAGCTCCAGAAGGAGCCCCCCTTCTGCAGG AGGAGCCGGGTCGGCTGGCGGGGGAGGCGGGGCTGGAGCTCCAGAAGGAGCCCCCCTTCTGCAGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14488051..14488175 26863196 MeRIP-seq:(Medium) rs772904946 Functional Loss SNV dbSNP153 33..33 33 - - - 56277 RMVar_ID_56277 Human_SNP_ID_222445169 m1A Human chr5 + 14611398 14611398 14611398 AATATGGAAGAACGGTTAGAGAGAGATGCACCATTGCTGGCTTTGAAGATGGAGGAAGGGGCCAT AATATGGAAGAACGGTTAGAGAGAGATGCACCGTTGCTGGCTTTGAAGATGGAGGAAGGGGCCAT A G OTULINL Ensembl:ENSG00000145569 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:14611347..14611447 26863196 MeRIP-seq:(Medium) rs1401213422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7402523 RMVar_hsa_circ_230450 56278 RMVar_ID_56278 Human_SNP_ID_222453289 m1A Human chr5 - 14639458 14639458 14639458 TGATTGCCACCAACATTCTCTTGGTTGATGAGATCATGCAAGCTGGAATGTTTTCTCTGAAAGGT TGATTGCCACCAACATTCTCTTGGTTGATGAGGTCATGCAAGCTGGAATGTTTTCTCTGAAAGGT T C CCT6P2 Ensembl:ENSG00000250526 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1198571377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1893540 56279 RMVar_ID_56279 Human_SNP_ID_222459498 m1A Human chr5 + 14664974 14664974 14664974 GCAGCCGCGGCCCGAGATGCAGTGCCCGGCCGAGCAGTGAGTCCGCGGGGGCGCGGGGCGCGGGC GCAGCCGCGGCCCGAGATGCAGTGCCCGGCCGCGCAGTGAGTCCGCGGGGGCGCGGGGCGCGGGC A C OTULIN Ensembl:ENSG00000154124 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:14664693..14665040 26863196 MeRIP-seq:(Medium) rs983896316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944135,Human_RBP_ID_23050392 Human_Splice_Rec_636647,Human_Splice_Rec_636655,Human_Splice_Rec_636667 56280 RMVar_ID_56280 Human_SNP_ID_222461558 m1A Human chr5 + 14673590 14673590 14673590 ATGCATTTGTAAGCAGCTGTATAATAGGACGGAAAATGTCAGTGCAACAAGTGTTTGAAAATGTC ATGCATTTGTAAGCAGCTGTATAATAGGACGGGAAATGTCAGTGCAACAAGTGTTTGAAAATGTC A G OTULIN Ensembl:ENSG00000154124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14673586..14673725 26863196 MeRIP-seq:(Medium) rs934627877 Functional Loss SNV dbSNP153 33..33 33 - - - 56281 RMVar_ID_56281 Human_SNP_ID_222469338 m1A Human chr5 + 14705810 14705810 14705810 TTGATGTGTACCCTGTACTCCTTTGTTACGCAAGGGTGGTTTGAACTTAGCTTTCAGTAGCTGTT TTGATGTGTACCCTGTACTCCTTTGTTACGCAGGGGTGGTTTGAACTTAGCTTTCAGTAGCTGTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:14705770..14705854 32194978 MeRIP-seq:(Medium) rs953828126 Functional Loss SNV dbSNP153 33..33 33 - - - 56282 RMVar_ID_56282 Human_SNP_ID_222470742 m1A Human chr5 + 14710852 14710852 14710852 CCTGCTGTGCAGGGTGACCGAGGCGCGATGGCACAGCTGCAGTCCTTTGGTTCCAAGAGGAGATT CCTGCTGTGCAGGGTGACCGAGGCGCGATGGCCCAGCTGCAGTCCTTTGGTTCCAAGAGGAGATT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:14710801..14710875 26863196 MeRIP-seq:(Medium) rs1279816942 Functional Loss SNV dbSNP153 33..33 33 - - - 56283 RMVar_ID_56283 Human_SNP_ID_222470778 m1A Human chr5 + 14710955 14710954 14710955 CTGTGTCTTTTGGGTTTTCGTGAGGCAGGGGTATGAAGTCAGTTGTTTCGTTTGTTTTTACATAG CTGTGTCTTTTGGGTTTTCGTGAGGCAGGGGT_TGAAGTCAGTTGTTTCGTTTGTTTTTACATAG TA T piR-35959 RNACentral:URS0000559145 piRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14710926..14710975 26863196 MeRIP-seq:(Medium) rs112207047 Functional Loss DEL dbSNP153 33..33 33 - - - 56284 RMVar_ID_56284 Human_SNP_ID_222470779 m1A Human chr5 + 14710955 14710955 14710955 CTGTGTCTTTTGGGTTTTCGTGAGGCAGGGGTATGAAGTCAGTTGTTTCGTTTGTTTTTACATAG CTGTGTCTTTTGGGTTTTCGTGAGGCAGGGGTTTGAAGTCAGTTGTTTCGTTTGTTTTTACATAG A T piR-35959 RNACentral:URS0000559145 piRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:14710926..14710975 26863196 MeRIP-seq:(Medium) rs573842770 Functional Loss SNV dbSNP153 33..33 33 - - - 56285 RMVar_ID_56285 Human_SNP_ID_222470897 m1A Human chr5 - 14711226 14711226 14711226 CAGACATGCCTCCGACAGAGGAGGTGACAGACATCGTGGAAATGAGAGAGGAGAATGAATAAGGC CAGACATGCCTCCGACAGAGGAGGTGACAGACGTCGTGGAAATGAGAGAGGAGAATGAATAAGGC T C ANKH Ensembl:ENSG00000154122 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:14711176..14711275 26863196 MeRIP-seq:(Medium) rs780455327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7402998,Human_RBP_ID_27512656 Human_Splice_Rec_636700,Human_Splice_Rec_636706 56286 RMVar_ID_56286 Human_SNP_ID_222471237 m1A Human chr5 - 14712203 14712203 14712203 AGAGCCTGCTCACGGTGCGTGACGTGCATCTCAGGACACTGGCTGTCCCCTGCGGTTGGGCTTCC AGAGCCTGCTCACGGTGCGTGACGTGCATCTCGGGACACTGGCTGTCCCCTGCGGTTGGGCTTCC T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:14712200..14712299 26863196 MeRIP-seq:(Medium) rs1018151153 Functional Loss SNV dbSNP153 33..33 33 - - - 56287 RMVar_ID_56287 Human_SNP_ID_222492161 m1A Human chr5 - 14797980 14797980 14797980 CCCGTTATATGCCCCAGAACCCTTGTATCATCACAACAAAGACTCCTTCCAGTGATATTCTTGTC CCCGTTATATGCCCCAGAACCCTTGTATCATCGCAACAAAGACTCCTTCCAGTGATATTCTTGTC T C ANKH,RBBP4P1 Ensembl:ENSG00000154122,Ensembl:ENSG00000249485 Protein coding,Pseudogene intron,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1209776064 Functional Loss SNV dbSNP153 33..33 33 - - - 56288 RMVar_ID_56288 Human_SNP_ID_222492588 m1A Human chr5 + 14799778 14799778 14799778 ACCTGGTCACCGAAGAGCTCTGATGGAGAGGTACGAGGAGATTTATGTTGTTTTCATGACTGCTA ACCTGGTCACCGAAGAGCTCTGATGGAGAGGTGCGAGGAGATTTATGTTGTTTTCATGACTGCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:14799773..14799881 26863196 MeRIP-seq:(Medium) rs955092058 Functional Loss SNV dbSNP153 33..33 33 - - - 56289 RMVar_ID_56289 Human_SNP_ID_222509521 m1A Human chr5 - 14871607 14871585 14871607 GCTAGAGCAGCCGCGCTCGGAGAAGGCGCCGCAGCCGCGAGGAGGAGCCGCCGCCGCCGCGCCCG GCTAGAGCAGCCGCGCTCGGAGAAGGCGCCGC______________________CGCCGCGCCCG GGCGGCGGCTCCTCCTCGCGGCT G ANKH Ensembl:ENSG00000154122 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:14871536..14871649 26863196 MeRIP-seq:(Medium) rs1011824945 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_4816538,Human_RBP_ID_22459116 56290 RMVar_ID_56290 Human_SNP_ID_468789618 m1A Human chr11 + 60842880 60842880 60842880 TCGGGGCGAGTGTGGAAGGACCGCTCCAAGAAAAGGTGAAGTGGGGGACAGCATGGACAGGGGTG TCGGGGCGAGTGTGGAAGGACCGCTCCAAGAATAGGTGAAGTGGGGGACAGCATGGACAGGGGTG A T CCDC86 Ensembl:ENSG00000110104 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60842076..60842900 26863196 MeRIP-seq:(Medium) rs1203218608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1244097,Human_Splice_Rec_1244105 56291 RMVar_ID_56291 Human_SNP_ID_468791462 m1A Human chr11 + 60850272 60850272 60850272 AGAAGCAGCTGCGCTCCATTGAGAAGCGGGACACCCTGGCCCTGCTGCAGAAGCAGCCGCCCCAG AGAAGCAGCTGCGCTCCATTGAGAAGCGGGACGCCCTGGCCCTGCTGCAGAAGCAGCCGCCCCAG A G CCDC86 Ensembl:ENSG00000110104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:60850202..60850302 26863196 MeRIP-seq:(Medium) rs1296160561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1244102,Human_Splice_Rec_1244110,Human_Splice_Rec_1244114,Human_Splice_Rec_1244120 56292 RMVar_ID_56292 Human_SNP_ID_468791482 m1A Human chr11 + 60850313 60850313 60850313 CTGCTGCAGAAGCAGCCGCCCCAGCAGCCGGCAGCCAAGATCTGAGCTCAGGACGGCCCGAGGCC CTGCTGCAGAAGCAGCCGCCCCAGCAGCCGGCGGCCAAGATCTGAGCTCAGGACGGCCCGAGGCC A G CCDC86 Ensembl:ENSG00000110104 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60850265..60850331 26863196 MeRIP-seq:(Medium) rs750127613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5165564 56293 RMVar_ID_56293 Human_SNP_ID_468791559 m1A Human chr11 - 60850582 60850580 60850583 TGTACAGTTCTTGGTTTGAAGGCACTTGGAGAAGGAGAGGAAGGAGGGATGGGAGCTGAATCTCT TGTACAGTTCTTGGTTTGAAGGCACTTGGAG___GAGAGGAAGGAGGGATGGGAGCTGAATCTCT CCTT C AP000777.3 Ensembl:ENSG00000256813 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr11:60850532..60850737;chr11:60847957..60850583 26863196,32194978 MeRIP-seq:(Medium) rs751367318 Functional Loss DEL dbSNP153 32..34 33 - - - 56294 RMVar_ID_56294 Human_SNP_ID_468803474 m1A Human chr11 - 60898930 60898930 60898930 CTGACTCCATTGTCTCTTTTTTTTTCCCCAGTACTGGGCTTTCTCTGACATCCAGACAGGGCGTG CTGACTCCATTGTCTCTTTTTTTTTCCCCAGTGCTGGGCTTTCTCTGACATCCAGACAGGGCGTG T C PRPF19 Ensembl:ENSG00000110107 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:60898926..60898950 26863196 MeRIP-seq:(Medium) rs1211377687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3376685,Human_RBP_ID_4164312,Human_RBP_ID_8770117,Human_RBP_ID_11650089 Human_Splice_Rec_1244194,Human_Splice_Rec_1244195,Human_Splice_Rec_1244209,Human_Splice_Rec_1244216,Human_Splice_Rec_1244217 RMVar_hsa_circ_63437,RMVar_hsa_circ_124507,RMVar_hsa_circ_125655,RMVar_hsa_circ_122566,RMVar_hsa_circ_149887,RMVar_hsa_circ_88650,RMVar_hsa_circ_93405,RMVar_hsa_circ_149889,RMVar_hsa_circ_81564,RMVar_hsa_circ_149890,RMVar_hsa_circ_149888,RMVar_hsa_circ_149885,RMVar_hsa_circ_149886,RMVar_hsa_circ_41677 56295 RMVar_ID_56295 Human_SNP_ID_468803528 m1A Human chr11 + 60899127 60899127 60899127 ATGTTCAAGCTTGGGGACCAGCAGGCCTCTCCAGGGCACTGGCTGGGACCGCACCTGATCATCGG ATGTTCAAGCTTGGGGACCAGCAGGCCTCTCCTGGGCACTGGCTGGGACCGCACCTGATCATCGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:60899126..60899200;chr11:60899126..60899150;chr11:60899126..60899300 26863196 MeRIP-seq:(Medium) rs1565110698 Functional Loss SNV dbSNP153 33..33 33 - - - 56296 RMVar_ID_56296 Human_SNP_ID_468803560 m1A Human chr11 + 60899218 60899218 60899218 GCATGAAGGCTGAGGCCTGTCACAGCACTCTCATGGGCCCGAACCACCTGTACACAAGAGGCATT GCATGAAGGCTGAGGCCTGTCACAGCACTCTCGTGGGCCCGAACCACCTGTACACAAGAGGCATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:60899151..60899275 32194978 MeRIP-seq:(Medium) rs746595209 Functional Loss SNV dbSNP153 33..33 33 - - - 56297 RMVar_ID_56297 Human_SNP_ID_468803572 m1A Human chr11 + 60899248 60899248 60899248 TCATGGGCCCGAACCACCTGTACACAAGAGGCATTGGGGACCGACCAAATCCTGATAGTGGCATC TCATGGGCCCGAACCACCTGTACACAAGAGGCTTTGGGGACCGACCAAATCCTGATAGTGGCATC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:60899226..60899250 26863196 MeRIP-seq:(Medium) rs1195839701 Functional Loss SNV dbSNP153 33..33 33 - - - 56298 RMVar_ID_56298 Human_SNP_ID_468804375 m1A Human chr11 - 60902482 60902482 60902482 GGTGTCTTTGGTGCTCTGTGCCTCTCACCCTCACCTTTCTTCTCTTCAGGGTGCGGGTGAGCCAA GGTGTCTTTGGTGCTCTGTGCCTCTCACCCTCGCCTTTCTTCTCTTCAGGGTGCGGGTGAGCCAA T C PRPF19 Ensembl:ENSG00000110107 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60902479..60902565 26863196 MeRIP-seq:(Medium) rs200606452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5345163,Human_RBP_ID_22641220 Human_Splice_Rec_1244183,Human_Splice_Rec_1244203,Human_Splice_Rec_1244235,Human_Splice_Rec_1244255 RMVar_hsa_circ_122566,RMVar_hsa_circ_93405,RMVar_hsa_circ_149889,RMVar_hsa_circ_149890,RMVar_hsa_circ_36502,RMVar_hsa_circ_41677 56299 RMVar_ID_56299 Human_SNP_ID_468807204 m1A Human chr11 - 60914226 60914226 60914226 CCACTGCTATCCTTCACGTGCGACTTCGCTGAAACGCGCCACCAAACCCGCGCCTCAACTCGGGG CCACTGCTATCCTTCACGTGCGACTTCGCTGAGACGCGCCACCAAACCCGCGCCTCAACTCGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:60914120..60925253;chr11:60914151..60914347;chr11:60914151..60914337 26863196 MeRIP-seq:(Medium) rs1320704465 Functional Loss SNV dbSNP153 33..33 33 - - - 56300 RMVar_ID_56300 Human_SNP_ID_468809120 m1A Human chr11 + 60922171 60922171 60922171 GGGGCCCGCAGTGTGGAGGAGGAGTGAGCCGGATGCCCCACACACCGCCAGTGTCATACCAAAGA GGGGCCCGCAGTGTGGAGGAGGAGTGAGCCGGTTGCCCCACACACCGCCAGTGTCATACCAAAGA A T TMEM109 Ensembl:ENSG00000110108 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60921951..60922359 26863196 MeRIP-seq:(Medium) rs1362287186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22433541 Human_miRNA_ID_2076073 RMVar_hsa_circ_149895,RMVar_hsa_circ_88537 56301 RMVar_ID_56301 Human_SNP_ID_468809243 m1A Human chr11 - 60922509 60922509 60922509 ATTAGGAGGAAGCCAAGGCAGCAGCAGAGGGAAGCCAGTTAAGTCATGAGAGACCAACGGCAGTG ATTAGGAGGAAGCCAAGGCAGCAGCAGAGGGAGGCCAGTTAAGTCATGAGAGACCAACGGCAGTG T C AP003721.1 Ensembl:ENSG00000256196 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60922458..60922607 26863196 MeRIP-seq:(Medium) rs1202854323 Functional Loss SNV dbSNP153 33..33 33 - - - 56302 RMVar_ID_56302 Human_SNP_ID_468809247 m1A Human chr11 - 60922541 60922541 60922541 GAGCAACTTCAGAAGGACAGGAGAGCACGAGCATTAGGAGGAAGCCAAGGCAGCAGCAGAGGGAA GAGCAACTTCAGAAGGACAGGAGAGCACGAGCGTTAGGAGGAAGCCAAGGCAGCAGCAGAGGGAA T C AP003721.1 Ensembl:ENSG00000256196 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60922491..60922595 26863196 MeRIP-seq:(Medium) rs1243821112 Functional Loss SNV dbSNP153 33..33 33 - - - 56303 RMVar_ID_56303 Human_SNP_ID_468809769 m1A Human chr11 + 60924534 60924534 60924534 GGCGGCGGCGGCGGCGGCGGCGGCCGGGACCCAGCGGGCCAGGTGGGGACGGCGCGGAGCGGGTG GGCGGCGGCGGCGGCGGCGGCGGCCGGGACCCGGCGGGCCAGGTGGGGACGGCGCGGAGCGGGTG A G TMEM132A Ensembl:ENSG00000006118 Protein coding exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:60924496..60924581 26863410 MeRIP-seq:(Medium) rs1232502980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227461,Human_RBP_ID_751909,Human_RBP_ID_807007,Human_RBP_ID_4184064,Human_RBP_ID_18416822,Human_RBP_ID_18468924,Human_RBP_ID_22433542 Human_Splice_Rec_1244279 56304 RMVar_ID_56304 Human_SNP_ID_468810177 m1A Human chr11 - 60926104 60926104 60926104 GCCATGAGTGAATACTGCCTCCTTCTGAAGGAAGCCCTCCTTGGTTACTCACCTTCCCACCAGTC GCCATGAGTGAATACTGCCTCCTTCTGAAGGAGGCCCTCCTTGGTTACTCACCTTCCCACCAGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:60926068..60926230 26863196 MeRIP-seq:(Medium) rs1347532008 Functional Loss SNV dbSNP153 33..33 33 - - - 56305 RMVar_ID_56305 Human_SNP_ID_468810476 m1A Human chr11 - 60927252 60927252 60927252 CACGGAAGTGTTCAGGGGCGTCTAGGAGCTCCAGGGCTGCCGGCAGGTAGACAGGGTCCAGGGGA CACGGAAGTGTTCAGGGGCGTCTAGGAGCTCCGGGGCTGCCGGCAGGTAGACAGGGTCCAGGGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60927170..60927425 26863196 MeRIP-seq:(Medium) rs200112515 Functional Loss SNV dbSNP153 33..33 33 - - - 56306 RMVar_ID_56306 Human_SNP_ID_468811849 m1A Human chr11 - 60932075 60932075 60932075 CAGACTCGCAGCCGACATGCTCTGTCACCTCCACCAAGGCCCCCCCGCCGTCCACAGTGACAAGG CAGACTCGCAGCCGACATGCTCTGTCACCTCCGCCAAGGCCCCCCCGCCGTCCACAGTGACAAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:60932026..60932173 26863196 MeRIP-seq:(Medium) rs771785793 Functional Loss SNV dbSNP153 33..33 33 - - - 56307 RMVar_ID_56307 Human_SNP_ID_468812265 m1A Human chr11 - 60933648 60933648 60933648 TACGCAGCGGTAGCAGGGGGGCCCACACGGTCAGCCGCAGCGAGGCGCGGAGCCGGCGCCACCAG TACGCAGCGGTAGCAGGGGGGCCCACACGGTCTGCCGCAGCGAGGCGCGGAGCCGGCGCCACCAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:60933521..60933789;chr11:60933526..60933851;chr11:60933526..60933834;chr11:60933527..60933678 26863196 MeRIP-seq:(Medium) rs755673085 Functional Loss SNV dbSNP153 33..33 33 - - - 56308 RMVar_ID_56308 Human_SNP_ID_468812266 m1A Human chr11 - 60933648 60933648 60933648 TACGCAGCGGTAGCAGGGGGGCCCACACGGTCAGCCGCAGCGAGGCGCGGAGCCGGCGCCACCAG TACGCAGCGGTAGCAGGGGGGCCCACACGGTCGGCCGCAGCGAGGCGCGGAGCCGGCGCCACCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:60933521..60933789;chr11:60933526..60933851;chr11:60933526..60933834;chr11:60933527..60933678 26863196 MeRIP-seq:(Medium) rs755673085 Functional Loss SNV dbSNP153 33..33 33 - - - 56309 RMVar_ID_56309 Human_SNP_ID_468812884 m1A Human chr11 + 60935340 60935340 60935340 CGACAAGGTCTCAGTGCTGGAGCTGAGGGTGCAGCCAGTGATGGGCATCTCGCTGACCTTGAGCC CGACAAGGTCTCAGTGCTGGAGCTGAGGGTGCCGCCAGTGATGGGCATCTCGCTGACCTTGAGCC A C TMEM132A Ensembl:ENSG00000006118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60935291..60935502 26863196 MeRIP-seq:(Medium) rs1236803197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184069,Human_RBP_ID_17805881,Human_RBP_ID_18973654 Human_Splice_Rec_1244304,Human_Splice_Rec_1244324,Human_Splice_Rec_1244362,Human_Splice_Rec_1244364,Human_Splice_Rec_1244366 Human_miRNA_ID_2331913,Human_miRNA_ID_2964998 RMVar_hsa_circ_91410,RMVar_hsa_circ_149896 56310 RMVar_ID_56310 Human_SNP_ID_468812900 m1A Human chr11 + 60935385 60935385 60935385 CATCTCGCTGACCTTGAGCCGGGGCACTGCCCACCCCGGGGAGGTCACAGCTACGTGCTGGGCAC CATCTCGCTGACCTTGAGCCGGGGCACTGCCCCCCCCGGGGAGGTCACAGCTACGTGCTGGGCAC A C TMEM132A Ensembl:ENSG00000006118 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60935336..60935466 26863196 MeRIP-seq:(Medium) rs773646537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17805881,Human_RBP_ID_18468925,Human_RBP_ID_18973654,Human_RBP_ID_22434389 Human_Splice_Rec_1244305,Human_Splice_Rec_1244325,Human_Splice_Rec_1244367 RMVar_hsa_circ_91410,RMVar_hsa_circ_149896 56311 RMVar_ID_56311 Human_SNP_ID_468813533 m1A Human chr11 + 60936914 60936914 60936914 TGGAGAGGATCCGGGGCAGCTCCTGACCCTCCACAGCCACCTGGTCAGCCACCAGCTGGGGCAAC TGGAGAGGATCCGGGGCAGCTCCTGACCCTCCGCAGCCACCTGGTCAGCCACCAGCTGGGGCAAC A G TMEM132A Ensembl:ENSG00000006118 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60936864..60937041 26863196 MeRIP-seq:(Medium) rs1292965483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398233,Human_RBP_ID_748845,Human_RBP_ID_5111082,Human_RBP_ID_17805882 RMVar_hsa_circ_91410,RMVar_hsa_circ_149896 56312 RMVar_ID_56312 Human_SNP_ID_468813569 m1A Human chr11 - 60937013 60937013 60937013 GATGGGAGTCCTTGTGGGGGACCAGGCAGGGGACTTGGATCAACAAGCACCAGACGAGTGGCGGG GATGGGAGTCCTTGTGGGGGACCAGGCAGGGGTCTTGGATCAACAAGCACCAGACGAGTGGCGGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60936910..60937099 26863196 MeRIP-seq:(Medium) rs1214368564 Functional Loss SNV dbSNP153 33..33 33 - - - 56313 RMVar_ID_56313 Human_SNP_ID_468862245 m1A Human chr11 + 61131741 61131741 61131741 TCCACAGGGAGCACCAACGCCACTTCCAGTTGACCCTCGAATCTCGGCGATGGCTGGGCCAAAGG TCCACAGGGAGCACCAACGCCACTTCCAGTTGTCCCTCGAATCTCGGCGATGGCTGGGCCAAAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61131690..61131790 32194978 MeRIP-seq:(Medium) rs1331198498 Functional Loss SNV dbSNP153 33..33 33 - - - 56314 RMVar_ID_56314 Human_SNP_ID_468862306 m1A Human chr11 + 61131868 61131868 61131868 GCAGGCCCCGGCGGTGGTGGGAACCCATAGGGAGGGGCGGGCCCGGGGGGATAAGGGGGCTGCAG GCAGGCCCCGGCGGTGGTGGGAACCCATAGGGGGGGGCGGGCCCGGGGGGATAAGGGGGCTGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61131819..61131910 26863196 MeRIP-seq:(Medium) rs1444679227 Functional Loss SNV dbSNP153 33..33 33 - - - 56315 RMVar_ID_56315 Human_SNP_ID_468862374 m1A Human chr11 - 61132037 61132037 61132037 TGGGACCCCAATGGGTGCCTCTGGGCCTGGGTACCCCTTGCGGGGAGGCAGGGCCCCCAGTCCTG TGGGACCCCAATGGGTGCCTCTGGGCCTGGGTCCCCCTTGCGGGGAGGCAGGGCCCCCAGTCCTG T G VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61131987..61132334 32194978 MeRIP-seq:(Medium) rs1174772787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3023873 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 56316 RMVar_ID_56316 Human_SNP_ID_468862449 m1A Human chr11 - 61132229 61132229 61132229 ATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCATGGAGCCCTGCCACCGGCCCCTTTCCCAGTAG ATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCGTGGAGCCCTGCCACCGGCCCCTTTCCCAGTAG T C VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:61132182..61132384 26863196 MeRIP-seq:(Medium) rs2232143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126573,Human_RBP_ID_5234993,Human_RBP_ID_17073686 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 56317 RMVar_ID_56317 Human_SNP_ID_468862451 m1A Human chr11 - 61132236 61132236 61132236 ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCATGGAGCCCTGCCACCGGCCCCTTTC ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCGCTGCCCATGGAGCCCTGCCACCGGCCCCTTTC T C VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61132185..61132433 26863196 MeRIP-seq:(Medium) rs758133603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4164594,Human_RBP_ID_5126573,Human_RBP_ID_5234993,Human_RBP_ID_17073686 Human_miRNA_ID_1293141,Human_miRNA_ID_1297166,Human_miRNA_ID_1417445,Human_miRNA_ID_2457432,Human_miRNA_ID_2462352,Human_miRNA_ID_2634995,Human_miRNA_ID_2637682 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 56318 RMVar_ID_56318 Human_SNP_ID_468862482 m1A Human chr11 - 61132304 61132304 61132304 GGGAACACCCCCTGTGGTTGAAGAGCAGCCGCAGCCACCATTAGCCATGCCTCCCTACCCTTTGC GGGAACACCCCCTGTGGTTGAAGAGCAGCCGCGGCCACCATTAGCCATGCCTCCCTACCCTTTGC T C VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:61132255..61132418 26863196 MeRIP-seq:(Medium) rs1371262142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17797668 Human_miRNA_ID_231766,Human_miRNA_ID_1363853,Human_miRNA_ID_1368834,Human_miRNA_ID_2690003 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 56319 RMVar_ID_56319 Human_SNP_ID_468862564 m1A Human chr11 + 61132483 61132483 61132483 CGCAGGTGGGACAGCATCCTCATGGAGGAAAAATTCTCCAGGAACGTTTCCAGGGGCACCTCGCC CGCAGGTGGGACAGCATCCTCATGGAGGAAAAGTTCTCCAGGAACGTTTCCAGGGGCACCTCGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61132432..61132532 32194978 MeRIP-seq:(Medium) rs1357019509 Functional Loss SNV dbSNP153 33..33 33 - - - 56320 RMVar_ID_56320 Human_SNP_ID_468867138 m1A Human chr11 - 61150014 61150014 61150014 CCTTTAGGGGACGGACTGGGTCAGCAAAGCCAAGCCAGCGACCTAGGGGGCAGGGTGTGAGTGCT CCTTTAGGGGACGGACTGGGTCAGCAAAGCCAGGCCAGCGACCTAGGGGGCAGGGTGTGAGTGCT T C VPS37C Ensembl:ENSG00000167987 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61150012..61150381 26863196 MeRIP-seq:(Medium) rs1045312071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86556,RMVar_hsa_circ_149902 56321 RMVar_ID_56321 Human_SNP_ID_468891183 m1A Human chr11 + 61273192 61273192 61273192 ATCCATGCCCTGTGTCGGGGCAGCCCTGGACCAGCTCACCTGTCGAGGGTGTGGGCTCCTGGCAG ATCCATGCCCTGTGTCGGGGCAGCCCTGGACCGGCTCACCTGTCGAGGGTGTGGGCTCCTGGCAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:61273189..61273302 26863196 MeRIP-seq:(Medium) rs771976757 Functional Loss SNV dbSNP153 33..33 33 - - - 56322 RMVar_ID_56322 Human_SNP_ID_468897878 m1A Human chr11 + 61299980 61299980 61299980 TTCACCTTCAGCTCATTCCCAAGTCTCTATGAAGCCCGCCCCACTTCCACATAGGGGAACTGTGG TTCACCTTCAGCTCATTCCCAAGTCTCTATGAGGCCCGCCCCACTTCCACATAGGGGAACTGTGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:61299976..61300000 26863196 MeRIP-seq:(Medium) rs1243638327 Functional Loss SNV dbSNP153 33..33 33 - - - 56323 RMVar_ID_56323 Human_SNP_ID_468899608 m1A Human chr11 + 61306338 61306336 61306338 CTGTCCCTCATAGCACTGGAACAGGAGGTAGCACAGTCTCCCAAGCTCCTCGTCTGCTCTTTCAG CTGTCCCTCATAGCACTGGAACAGGAGGTAG__CAGTCTCCCAAGCTCCTCGTCTGCTCTTTCAG GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61306336..61306752 26863196 MeRIP-seq:(Medium) rs567451861 Functional Loss DEL dbSNP153 32..33 33 - - - 56324 RMVar_ID_56324 Human_SNP_ID_468900562 m1A Human chr11 + 61310362 61310362 61310362 TGCACCTCCACCTCTTCTCCAAAGGAGGTCTCATGAGGAGCAGTGCTGCTGGAGAACAGCTTGCT TGCACCTCCACCTCTTCTCCAAAGGAGGTCTCGTGAGGAGCAGTGCTGCTGGAGAACAGCTTGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61310276..61310456 32194978 MeRIP-seq:(Medium) rs1565240578 Functional Loss SNV dbSNP153 33..33 33 - - - 56325 RMVar_ID_56325 Human_SNP_ID_468901640 m1A Human chr11 + 61314051 61314051 61314051 CCAACCCAGGTCCCTAAATGACACATACCTCCACCCAGCATCTCCTTGTGCAGTAGTTCAAAAGA CCAACCCAGGTCCCTAAATGACACATACCTCCGCCCAGCATCTCCTTGTGCAGTAGTTCAAAAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61313846..61314124 32194978 MeRIP-seq:(Medium) rs778300971 Functional Loss SNV dbSNP153 33..33 33 - - - 56326 RMVar_ID_56326 Human_SNP_ID_468904249 m1A Human chr11 + 61323091 61323091 61323091 ATTATCAAGGTATGTCAAGCACTCAGCAATAGAGGTCTGGAAGAAAGTCAGCAACGTGAAAGAAA ATTATCAAGGTATGTCAAGCACTCAGCAATAGTGGTCTGGAAGAAAGTCAGCAACGTGAAAGAAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61323001..61323100 32194978 MeRIP-seq:(Medium) rs138285473 Functional Loss SNV dbSNP153 33..33 33 - - - 56327 RMVar_ID_56327 Human_SNP_ID_468905236 m1A Human chr11 - 61326835 61326835 61326835 CTATGAGGTGTCTCTCCGAGAAAAGGAATTCAATAAGGGCCCTTGGAAACAGGAAAATGTCGAAG CTATGAGGTGTCTCTCCGAGAAAAGGAATTCAGTAAGGGCCCTTGGAAACAGGAAAATGTCGAAG T C DDB1 Ensembl:ENSG00000167986 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61326776..61326908 32194978 MeRIP-seq:(Medium) rs755753291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31337,Human_RBP_ID_987522,Human_RBP_ID_1780333,Human_RBP_ID_3376751,Human_RBP_ID_4191472,Human_RBP_ID_17805592,Human_RBP_ID_22434415,Human_RBP_ID_27202783 Human_Splice_Rec_1244940,Human_Splice_Rec_1244941,Human_Splice_Rec_1245000,Human_Splice_Rec_1245001,Human_Splice_Rec_1245134,Human_Splice_Rec_1245135,Human_Splice_Rec_1245155,Human_Splice_Rec_1245169,Human_Splice_Rec_1245192,Human_Splice_Rec_1245193,Human_Splice_Rec_1245200,Human_Splice_Rec_1245201,Human_Splice_Rec_1245212 RMVar_hsa_circ_1866,RMVar_hsa_circ_56241,RMVar_hsa_circ_90525,RMVar_hsa_circ_94302,RMVar_hsa_circ_149933,RMVar_hsa_circ_149934,RMVar_hsa_circ_49773,RMVar_hsa_circ_103004,RMVar_hsa_circ_149956,RMVar_hsa_circ_116195,RMVar_hsa_circ_118249,RMVar_hsa_circ_149961,RMVar_hsa_circ_149962,RMVar_hsa_circ_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_112259,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149981,RMVar_hsa_circ_63857,RMVar_hsa_circ_51222,RMVar_hsa_circ_28398,RMVar_hsa_circ_313375,RMVar_hsa_circ_149986,RMVar_hsa_circ_149985,RMVar_hsa_circ_90530,RMVar_hsa_circ_336172,RMVar_hsa_circ_314781,RMVar_hsa_circ_328049,RMVar_hsa_circ_94839,RMVar_hsa_circ_15314,RMVar_hsa_circ_368672,RMVar_hsa_circ_149987,RMVar_hsa_circ_270991,RMVar_hsa_circ_149988,RMVar_hsa_circ_149989,RMVar_hsa_circ_278082,RMVar_hsa_circ_149990,RMVar_hsa_circ_149991 56328 RMVar_ID_56328 Human_SNP_ID_468905926 m1A Human chr11 + 61329514 61329514 61329514 GAATAACCTTGAAAAGGCCATCATAGAGACGCAGGCCAATCATCCGGCACTCAGGGTCAATGATG GAATAACCTTGAAAAGGCCATCATAGAGACGCTGGCCAATCATCCGGCACTCAGGGTCAATGATG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61329467..61329990 32194978 MeRIP-seq:(Medium) rs1312810571 Functional Loss SNV dbSNP153 33..33 33 - - - 56329 RMVar_ID_56329 Human_SNP_ID_468906098 m1A Human chr11 + 61330047 61330047 61330047 CTCCAGGATGCAGGCATTGTACTTCGCTGTCAAGATAAACAGCAGGTCCTTGCTCTCCCCCTGGA CTCCAGGATGCAGGCATTGTACTTCGCTGTCACGATAAACAGCAGGTCCTTGCTCTCCCCCTGGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61329996..61330099 26863196 MeRIP-seq:(Medium) rs748995718 Functional Loss SNV dbSNP153 33..33 33 - - - 56330 RMVar_ID_56330 Human_SNP_ID_468907431 m1A Human chr11 + 61334671 61334671 61334671 TGTACTCAGACCCAGGTAGCACAGGATTGTCCATCCTCCAGCAGCTCAGTGCAACGGTGTGAACT TGTACTCAGACCCAGGTAGCACAGGATTGTCCGTCCTCCAGCAGCTCAGTGCAACGGTGTGAACT A G TKFC Ensembl:ENSG00000149476 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61334601..61334725 26863196 MeRIP-seq:(Medium) rs1008451562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751339,Human_RBP_ID_4185824,Human_RBP_ID_22433570 Human_Splice_Rec_1245234,Human_Splice_Rec_1245235,Human_Splice_Rec_1245270,Human_Splice_Rec_1245271,Human_Splice_Rec_1245278,Human_Splice_Rec_1245279,Human_Splice_Rec_1245286,Human_Splice_Rec_1245287,Human_Splice_Rec_1245294,Human_Splice_Rec_1245295,Human_Splice_Rec_1245299,Human_Splice_Rec_1245302,Human_Splice_Rec_1245303,Human_Splice_Rec_1245308,Human_Splice_Rec_1245309,Human_Splice_Rec_1245315 Human_miRNA_ID_1024057 RMVar_hsa_circ_305568 56331 RMVar_ID_56331 Human_SNP_ID_468916719 m1A Human chr11 + 61368876 61368875 61368877 TCAAGAAGGAAGATCCTCCCTCTTGCACAATTAGAGTGTCCCCATCGGTCTCCAGTGCGGCATCC TCAAGAAGGAAGATCCTCCCTCTTGCACAATT__AGTGTCCCCATCGGTCTCCAGTGCGGCATCC TAG T TMEM138 Ensembl:ENSG00000149483 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61368826..61369093 26863196 MeRIP-seq:(Medium) rs1316492986 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4164960,Human_RBP_ID_11652071,Human_RBP_ID_26404604 56332 RMVar_ID_56332 Human_SNP_ID_468916731 m1A Human chr11 + 61368923 61368923 61368923 GTCTCCAGTGCGGCATCCCTTCCTTGCCTTCTACCTCTGTTCCACCCCCTTTCCTTCCTTTCCTC GTCTCCAGTGCGGCATCCCTTCCTTGCCTTCTGCCTCTGTTCCACCCCCTTTCCTTCCTTTCCTC A G TMEM138 Ensembl:ENSG00000149483 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61368873..61369111 26863196 MeRIP-seq:(Medium) rs1266728479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1354574,Human_RBP_ID_18932417,Human_RBP_ID_19648685,Human_RBP_ID_22035247,Human_RBP_ID_27417441 Human_miRNA_ID_663,Human_miRNA_ID_4312,Human_miRNA_ID_7990,Human_miRNA_ID_11527,Human_miRNA_ID_15075,Human_miRNA_ID_18741,Human_miRNA_ID_22372,Human_miRNA_ID_26019,Human_miRNA_ID_490574,Human_miRNA_ID_493833,Human_miRNA_ID_1165624,Human_miRNA_ID_1284939,Human_miRNA_ID_1305683 56333 RMVar_ID_56333 Human_SNP_ID_468922667 m1A Human chr11 - 61393273 61393273 61393273 GCAGGAAATAGGTAGCATTATACCACCCGTTCAGAAAGAACAGGATTTCCAGCGGGGTGGAGGAC GCAGGAAATAGGTAGCATTATACCACCCGTTCTGAAAGAACAGGATTTCCAGCGGGGTGGAGGAC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61392671..61394020 32194978 MeRIP-seq:(Medium) rs1237902679 Functional Loss SNV dbSNP153 33..33 33 - - - 56334 RMVar_ID_56334 Human_SNP_ID_468925088 m1A Human chr11 + 61403173 61403173 61403173 TCCAATCCTGCGGGGGACTCCCTCAGTGACTGAGGGCTATATGAGAAACGTGCTGGGAACAGAGG TCCAATCCTGCGGGGGACTCCCTCAGTGACTGGGGGCTATATGAGAAACGTGCTGGGAACAGAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61402989..61403190 32194978 MeRIP-seq:(Medium) rs180819290 Functional Loss SNV dbSNP153 33..33 33 - - - 56335 RMVar_ID_56335 Human_SNP_ID_468928272 m1A Human chr11 + 61416184 61416184 61416184 TGGAGGCCCCACTGTAGCGTTTGGTGGGGGGAAGAAGGCTGGATTGAGGTGAAGGGCAGGTGGGA TGGAGGCCCCACTGTAGCGTTTGGTGGGGGGAGGAAGGCTGGATTGAGGTGAAGGGCAGGTGGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:61416151..61416434 26863196 MeRIP-seq:(Medium) rs1161093871 Functional Loss SNV dbSNP153 33..33 33 - - - 56336 RMVar_ID_56336 Human_SNP_ID_468929700 m1A Human chr11 + 61421548 61421548 61421548 AGTGCTGCTGCTTCTGTCATCTGAGGGCTGTGAGGTGGCTGTCAGCACATCATCATACAGGTCAA AGTGCTGCTGCTTCTGTCATCTGAGGGCTGTGGGGTGGCTGTCAGCACATCATCATACAGGTCAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:61421521..61421634 26863196 MeRIP-seq:(Medium) rs1363189418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780414 56337 RMVar_ID_56337 Human_SNP_ID_468931795 m1A Human chr11 - 61429146 61429146 61429146 AGGTGTCATCAGGAGCTTTGGGATTTTCCTTGATCATCTGAGGAATCATTTTCAGCAAACTGGCA AGGTGTCATCAGGAGCTTTGGGATTTTCCTTGGTCATCTGAGGAATCATTTTCAGCAAACTGGCA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61429144..61429300 26863196 MeRIP-seq:(Medium) rs759025416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11653331,Human_RBP_ID_22353328 RMVar_hsa_circ_333194,RMVar_hsa_circ_150024,RMVar_hsa_circ_101153,RMVar_hsa_circ_150026,RMVar_hsa_circ_331840,RMVar_hsa_circ_312656,RMVar_hsa_circ_330660,RMVar_hsa_circ_150027 56338 RMVar_ID_56338 Human_SNP_ID_468931803 m1A Human chr11 - 61429186 61429186 61429186 CTTGATTGATATATATGCTGACGAGGAGTTCAACCAGGTGAGGTGTCATCAGGAGCTTTGGGATT CTTGATTGATATATATGCTGACGAGGAGTTCAGCCAGGTGAGGTGTCATCAGGAGCTTTGGGATT T C CPSF7 Ensembl:ENSG00000149532 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61429160..61429975 26863196 MeRIP-seq:(Medium) rs1487664300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398449,Human_RBP_ID_1457986,Human_RBP_ID_1780422,Human_RBP_ID_3376838,Human_RBP_ID_4184903,Human_RBP_ID_9362311,Human_RBP_ID_18973740,Human_RBP_ID_22435305,Human_RBP_ID_23510298 Human_Splice_Rec_1245633,Human_Splice_Rec_1245651,Human_Splice_Rec_1245669,Human_Splice_Rec_1245687,Human_Splice_Rec_1245705,Human_Splice_Rec_1245713,Human_Splice_Rec_1245731,Human_Splice_Rec_1245739,Human_Splice_Rec_1245749,Human_Splice_Rec_1245759,Human_Splice_Rec_1245769,Human_Splice_Rec_1245779,Human_Splice_Rec_1245789,Human_Splice_Rec_1245799,Human_Splice_Rec_1245807,Human_Splice_Rec_1245815,Human_Splice_Rec_1245825,Human_Splice_Rec_1245831,Human_Splice_Rec_1245839,Human_Splice_Rec_1245845,Human_Splice_Rec_1245855,Human_Splice_Rec_1245863,Human_Splice_Rec_1245867,Human_Splice_Rec_1245873 RMVar_hsa_circ_333194,RMVar_hsa_circ_150024,RMVar_hsa_circ_101153,RMVar_hsa_circ_7842,RMVar_hsa_circ_150026,RMVar_hsa_circ_331840,RMVar_hsa_circ_312656,RMVar_hsa_circ_330660,RMVar_hsa_circ_150027 56339 RMVar_ID_56339 Human_SNP_ID_468931837 m1A Human chr11 + 61429274 61429274 61429274 GGAAGGAAGATCGCGAGTCCGGAGGATGGACAAAGTAAGGAAGATGCCACTGCGGGATTCGGAAA GGAAGGAAGATCGCGAGTCCGGAGGATGGACAGAGTAAGGAAGATGCCACTGCGGGATTCGGAAA A G AP003108.2 Ensembl:ENSG00000256591 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:61429150..61430074 26863196 MeRIP-seq:(Medium) rs770697040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1245879 56340 RMVar_ID_56340 Human_SNP_ID_468931990 m1A Human chr11 - 61429626 61429626 61429626 GGCCGGAGCCGCCTTGGGGGCTAGGCAGGTGCAGCGGATAGGGGCTGCGGGCTTCGCCGCGGTCA GGCCGGAGCCGCCTTGGGGGCTAGGCAGGTGCGGCGGATAGGGGCTGCGGGCTTCGCCGCGGTCA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:61429621..61429950;chr11:61429623..61429975 26863196 MeRIP-seq:(Medium) rs1395536862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385037,Human_RBP_ID_5313606,Human_RBP_ID_5345214,Human_RBP_ID_8174198,Human_RBP_ID_8229529,Human_RBP_ID_9414132,Human_RBP_ID_18932423,Human_RBP_ID_19054850,Human_RBP_ID_22708737 56341 RMVar_ID_56341 Human_SNP_ID_468940839 m1A Human chr11 - 61463966 61463957 61463967 GGAGGGGAGGGGAGGGGAGGGAAGGGAAGGGAAGGGAAGGGTAGGGAAGGGAAGGGAAGGGAAGG GGAGGGGAGGGGAGGGGAGGGAAGGGAAGGG__________TAGGGAAGGGAAGGGAAGGGAAGG ACCCTTCCCTT A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:61463936..61464018 26863410 MeRIP-seq:(Medium) rs1197089916 Functional Loss DEL dbSNP153 32..41 33 - - - 56342 RMVar_ID_56342 Human_SNP_ID_468940840 m1A Human chr11 - 61463966 61463957 61463967 GGAGGGGAGGGGAGGGGAGGGAAGGGAAGGGAAGGGAAGGGTAGGGAAGGGAAGGGAAGGGAAGG GGAGGGGAGGGGAGGGGAGGGAAGGGAAGGG_____AAGGGTAGGGAAGGGAAGGGAAGGGAAGG ACCCTTCCCTT ACCCTT - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:61463936..61464018 26863410 MeRIP-seq:(Medium) rs1197089916 Functional Loss DEL dbSNP153 32..36 33 - - - 56343 RMVar_ID_56343 Human_SNP_ID_468964496 m1A Human chr11 + 61553704 61553704 61553704 AGGGTCCAGGTGACATTAGGCAGCTCCAAAGCAGCCCAACACCACCAGCCTGCTTCTCAGGGAGG AGGGTCCAGGTGACATTAGGCAGCTCCAAAGCCGCCCAACACCACCAGCCTGCTTCTCAGGGAGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:61553701..61553750 26863196 MeRIP-seq:(Medium) rs1247646761 Functional Loss SNV dbSNP153 33..33 33 - - - 56344 RMVar_ID_56344 Human_SNP_ID_468970710 m1A Human chr11 - 61580996 61580996 61580996 GGCGGCGGCAGCGTGCTCCGCGGGCGGGCGGGAGGGCTGGCGGGCGGCCCCCGCTCCCCGGCTCC GGCGGCGGCAGCGTGCTCCGCGGGCGGGCGGGGGGGCTGGCGGGCGGCCCCCGCTCCCCGGCTCC T C SYT7 Ensembl:ENSG00000011347 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61580973..61581048 26863196 MeRIP-seq:(Medium) rs1205399125 Functional Loss SNV dbSNP153 33..33 33 - - - 56345 RMVar_ID_56345 Human_SNP_ID_468986608 m1A Human chr11 - 61644733 61644730 61644733 GGAGGCCAAGGCGGGTGGGTCACGTGGTCAGAAGATCAAGACCATCCTGGCTAACATGGTGAAAC GGAGGCCAAGGCGGGTGGGTCACGTGGTCAGA___TCAAGACCATCCTGGCTAACATGGTGAAAC ATCT A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:61644726..61644775 26863196 MeRIP-seq:(Medium) rs1168180842 Functional Loss DEL dbSNP153 33..35 33 - - - 56346 RMVar_ID_56346 Human_SNP_ID_468995891 m1A Human chr11 + 61680448 61680448 61680448 GGAAGCGGCGTTAGTGAATCGGGGCCTTGGGGAGCCCAGGATGGAGGTGGCGGTCGCGGCGGCGG GGAAGCGGCGTTAGTGAATCGGGGCCTTGGGGGGCCCAGGATGGAGGTGGCGGTCGCGGCGGCGG A G DAGLA Ensembl:ENSG00000134780 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:61680443..61680572 26863196 MeRIP-seq:(Medium) rs970555901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1246319,Human_Splice_Rec_1246357 56347 RMVar_ID_56347 Human_SNP_ID_469011152 m1A Human chr11 + 61743816 61743816 61743816 CCTCCACGCTGTGCTGGAGCGTGATGAAGGCCACCTCTTCTACATTGACCCTGCCATCCCCGAGG CCTCCACGCTGTGCTGGAGCGTGATGAAGGCCGCCTCTTCTACATTGACCCTGCCATCCCCGAGG A G DAGLA Ensembl:ENSG00000134780 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61743767..61743893 26863196 MeRIP-seq:(Medium) rs755165892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27202954,Human_RBP_ID_27412725,Human_RBP_ID_27556929 56348 RMVar_ID_56348 Human_SNP_ID_469013534 m1A Human chr11 + 61752623 61752623 61752623 CAGGGACGCGCGGGGGGCAAGCGCGGCGGCGGACCGGGCGGGACCGTAGCCGGAGCCCAGCCGGG CAGGGACGCGCGGGGGGCAAGCGCGGCGGCGGGCCGGGCGGGACCGTAGCCGGAGCCCAGCCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61752618..61752710 26863196 MeRIP-seq:(Medium) rs1010351048 Functional Loss SNV dbSNP153 33..33 33 - - - 56349 RMVar_ID_56349 Human_SNP_ID_469023735 m1A Human chr11 - 61790570 61790570 61790570 GAGCTCGAGGCCATGAGCAGATATACCAGCCCAGTGAACCCAGCTGTCTTCCCCCATCTGACCGT GAGCTCGAGGCCATGAGCAGATATACCAGCCCCGTGAACCCAGCTGTCTTCCCCCATCTGACCGT T G TMEM258 Ensembl:ENSG00000134825 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:61790501..61790650 26863410 MeRIP-seq:(Medium) rs1359918785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398540,Human_RBP_ID_749588,Human_RBP_ID_871730,Human_RBP_ID_1780435,Human_RBP_ID_4165242,Human_RBP_ID_5111095,Human_RBP_ID_5313609,Human_RBP_ID_5345252,Human_RBP_ID_9004540,Human_RBP_ID_17648690,Human_RBP_ID_22434448 Human_Splice_Rec_1246573,Human_Splice_Rec_1246582,Human_Splice_Rec_1246583,Human_Splice_Rec_1246588,Human_Splice_Rec_1246594,Human_Splice_Rec_1246600,Human_Splice_Rec_1246601,Human_Splice_Rec_1246606,Human_Splice_Rec_1246610,Human_Splice_Rec_1246611,Human_Splice_Rec_1246616 Human_miRNA_ID_2554014,Human_miRNA_ID_3057583 RMVar_hsa_circ_118504,RMVar_hsa_circ_111794,RMVar_hsa_circ_150065,RMVar_hsa_circ_150066,RMVar_hsa_circ_270467 56350 RMVar_ID_56350 Human_SNP_ID_469024273 m1A Human chr11 + 61792554 61792554 61792554 CATCTCCGTCTGGAACTCCCCTCAACGCTCTCACCATTTTGCCCCGCGAAGGCTAATCCGCCGCT CATCTCCGTCTGGAACTCCCCTCAACGCTCTCCCCATTTTGCCCCGCGAAGGCTAATCCGCCGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61792551..61792600 26863196 MeRIP-seq:(Medium) rs111585800 Functional Loss SNV dbSNP153 33..33 33 - - - 56351 RMVar_ID_56351 Human_SNP_ID_469024274 m1A Human chr11 + 61792554 61792554 61792554 CATCTCCGTCTGGAACTCCCCTCAACGCTCTCACCATTTTGCCCCGCGAAGGCTAATCCGCCGCT CATCTCCGTCTGGAACTCCCCTCAACGCTCTCTCCATTTTGCCCCGCGAAGGCTAATCCGCCGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61792551..61792600 26863196 MeRIP-seq:(Medium) rs111585800 Functional Loss SNV dbSNP153 33..33 33 - - - 56352 RMVar_ID_56352 Human_SNP_ID_469024438 m1A Human chr11 - 61792959 61792959 61792959 TGGTTCGGGGTTGCCCCGGGCAGGCGGTCCTAAGCTCGCTCTCCCTTCTCAGCTTAGCGGCGGGT TGGTTCGGGGTTGCCCCGGGCAGGCGGTCCTAGGCTCGCTCTCCCTTCTCAGCTTAGCGGCGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:61792737..61816937;chr11:61792901..61793059 26863196 MeRIP-seq:(Medium) rs1434871510 Functional Loss SNV dbSNP153 33..33 33 - - - 56353 RMVar_ID_56353 Human_SNP_ID_469025105 m1A Human chr11 - 61795576 61795576 61795576 ACACGGGCTTGATGCCGTTCTCCATCATGCGAATGGTGCGGTAGAACATGCCCATCAGGTGGCTG ACACGGGCTTGATGCCGTTCTCCATCATGCGAGTGGTGCGGTAGAACATGCCCATCAGGTGGCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61795526..61795575 32194978 MeRIP-seq:(Medium) rs756555908 Functional Loss SNV dbSNP153 33..33 33 - - - 56354 RMVar_ID_56354 Human_SNP_ID_469026618 m1A Human chr11 + 61802176 61802176 61802176 GCATGTGCCAAACTAGAAAAAGGAAATAATTTACACCCCTGCCCCAACAGCTCCTTCCCTCCTAG GCATGTGCCAAACTAGAAAAAGGAAATAATTTCCACCCCTGCCCCAACAGCTCCTTCCCTCCTAG A C FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61802126..61802275 32194978 MeRIP-seq:(Medium) rs368544311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8353607 56355 RMVar_ID_56355 Human_SNP_ID_469028077 m1A Human chr11 - 61808782 61808782 61808782 ATGGATTTGGGATATGTTTTGGAGGCAGTGTAAGCAACGCTTGCTGAGGACCTGGATGTGGTGGT ATGGATTTGGGATATGTTTTGGAGGCAGTGTATGCAACGCTTGCTGAGGACCTGGATGTGGTGGT T A FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:61808779..61809122 26863196 MeRIP-seq:(Medium) rs1342892395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17184455 RMVar_hsa_circ_113848,RMVar_hsa_circ_150072,RMVar_hsa_circ_150071,RMVar_hsa_circ_76265,RMVar_hsa_circ_347142,RMVar_hsa_circ_375961,RMVar_hsa_circ_150073,RMVar_hsa_circ_79334,RMVar_hsa_circ_92166,RMVar_hsa_circ_360869,RMVar_hsa_circ_370243,RMVar_hsa_circ_150080,RMVar_hsa_circ_150081,RMVar_hsa_circ_306330,RMVar_hsa_circ_150086,RMVar_hsa_circ_150084,RMVar_hsa_circ_270342 56356 RMVar_ID_56356 Human_SNP_ID_469029954 m1A Human chr11 - 61816312 61816309 61816313 GGGATGGAGGCCAACAACACGCACACACAAACAAAGGGTCCCGCCTCCCTGCCGTGCATTCCATC GGGATGGAGGCCAACAACACGCACACACAAA____GGGTCCCGCCTCCCTGCCGTGCATTCCATC CTTTG C FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:61816306..61816456 26863196 MeRIP-seq:(Medium) rs1402649962 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_2976,Human_RBP_ID_3384128,Human_RBP_ID_5313618 Human_Splice_Rec_1246889 56357 RMVar_ID_56357 Human_SNP_ID_469029955 m1A Human chr11 - 61816312 61816312 61816312 GGGATGGAGGCCAACAACACGCACACACAAACAAAGGGTCCCGCCTCCCTGCCGTGCATTCCATC GGGATGGAGGCCAACAACACGCACACACAAACGAAGGGTCCCGCCTCCCTGCCGTGCATTCCATC T C FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:61816306..61816456 26863196 MeRIP-seq:(Medium) rs1273462397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2976,Human_RBP_ID_3384128,Human_RBP_ID_5313618 Human_Splice_Rec_1246889 56358 RMVar_ID_56358 Human_SNP_ID_469030117 m1A Human chr11 + 61816742 61816742 61816742 GGGTAGGTCCCTGAGCCGCGGTCTCGGCGGCCACCGGGTCGGGGGCCATAGCTGGCCTGGCGACG GGGTAGGTCCCTGAGCCGCGGTCTCGGCGGCCGCCGGGTCGGGGGCCATAGCTGGCCTGGCGACG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61816725..61816875 32194978 MeRIP-seq:(Medium) rs1296296613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22569231 56359 RMVar_ID_56359 Human_SNP_ID_469030118 m1A Human chr11 + 61816742 61816742 61816742 GGGTAGGTCCCTGAGCCGCGGTCTCGGCGGCCACCGGGTCGGGGGCCATAGCTGGCCTGGCGACG GGGTAGGTCCCTGAGCCGCGGTCTCGGCGGCCTCCGGGTCGGGGGCCATAGCTGGCCTGGCGACG A T FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61816725..61816875 32194978 MeRIP-seq:(Medium) rs1296296613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22569231 56360 RMVar_ID_56360 Human_SNP_ID_469030157 m1A Human chr11 - 61816818 61816818 61816818 CGCGCCAGCAAATCCACTCCTGGAGCCCGCGGACCCCGAGCACGCGCCTGACAGCCCCTGCTGGC CGCGCCAGCAAATCCACTCCTGGAGCCCGCGGGCCCCGAGCACGCGCCTGACAGCCCCTGCTGGC T C FADS1 Ensembl:ENSG00000149485 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:61816531..61816907 26863196 MeRIP-seq:(Medium) rs1366931525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227747,Human_RBP_ID_4184100,Human_RBP_ID_5489866,Human_RBP_ID_9321431,Human_RBP_ID_22433612,Human_RBP_ID_22532281,Human_RBP_ID_26803583,Human_RBP_ID_27417449 56361 RMVar_ID_56361 Human_SNP_ID_469033214 m1A Human chr11 + 61828256 61828256 61828256 GGCGAGAAGGCTGGGGGAGGGGGCGCGGTGGGAGGAGTAGGAGAAGACAAAAGCCGAAAGCGAAG GGCGAGAAGGCTGGGGGAGGGGGCGCGGTGGGGGGAGTAGGAGAAGACAAAAGCCGAAAGCGAAG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:61828114..61828375 26863196 MeRIP-seq:(Medium) rs974835304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3384137,Human_RBP_ID_5168410,Human_RBP_ID_8175742,Human_RBP_ID_9415471 56362 RMVar_ID_56362 Human_SNP_ID_469045911 m1A Human chr11 + 61876099 61876099 61876099 GACCCCCTCCCCACCTCCCACTGGCCCCCAGCACCCACACTCACTGGTGCTCGATCTGGAAGTTG GACCCCCTCCCCACCTCCCACTGGCCCCCAGCTCCCACACTCACTGGTGCTCGATCTGGAAGTTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61876090..61876185 26863196 MeRIP-seq:(Medium) rs1439187596 Functional Loss SNV dbSNP153 33..33 33 - - - 56363 RMVar_ID_56363 Human_SNP_ID_469046101 m1A Human chr11 - 61876597 61876597 61876597 ACAGTGGACACTGCTCCATTCAGATTCTTTAAACACTGGCAAGGGGGCGATGGCCACAATCCTAT ACAGTGGACACTGCTCCATTCAGATTCTTTAATCACTGGCAAGGGGGCGATGGCCACAATCCTAT T A FADS3 Ensembl:ENSG00000221968 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61876589..61876679 26863196 MeRIP-seq:(Medium) rs1449017806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32028,Human_RBP_ID_21965735,Human_RBP_ID_26318399,Human_RBP_ID_27804492 RMVar_hsa_circ_104890,RMVar_hsa_circ_126843,RMVar_hsa_circ_118092,RMVar_hsa_circ_20215,RMVar_hsa_circ_150113,RMVar_hsa_circ_84299,RMVar_hsa_circ_150111,RMVar_hsa_circ_150112,RMVar_hsa_circ_150110,RMVar_hsa_circ_90215,RMVar_hsa_circ_112220,RMVar_hsa_circ_150119,RMVar_hsa_circ_150120,RMVar_hsa_circ_88839,RMVar_hsa_circ_150121 56364 RMVar_ID_56364 Human_SNP_ID_469046250 m1A Human chr11 - 61876965 61876965 61876965 GACCTCTCGGTATCGCCTCTGCCCTCCTCTGCAGGATTTGCTCTGGGCCGCCAGCTTCTATGCCC GACCTCTCGGTATCGCCTCTGCCCTCCTCTGCCGGATTTGCTCTGGGCCGCCAGCTTCTATGCCC T G FADS3 Ensembl:ENSG00000221968 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61876926..61876975 32194978 MeRIP-seq:(Medium) rs112635718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1246975,Human_Splice_Rec_1247011,Human_Splice_Rec_1247043,Human_Splice_Rec_1247051,Human_Splice_Rec_1247073 RMVar_hsa_circ_104890,RMVar_hsa_circ_126843,RMVar_hsa_circ_118092,RMVar_hsa_circ_20215,RMVar_hsa_circ_150113,RMVar_hsa_circ_84299,RMVar_hsa_circ_150111,RMVar_hsa_circ_150112,RMVar_hsa_circ_150110,RMVar_hsa_circ_90215,RMVar_hsa_circ_112220,RMVar_hsa_circ_150119,RMVar_hsa_circ_84969,RMVar_hsa_circ_150121,RMVar_hsa_circ_150123 56365 RMVar_ID_56365 Human_SNP_ID_469046325 m1A Human chr11 + 61877272 61877270 61877272 CAGCAACTCCTCCTGGGAAGACACCCTCACCGAGAGAGACCCACACCCCCCCTGTTCCTCAACCC CAGCAACTCCTCCTGGGAAGACACCCTCACC__GAGAGACCCACACCCCCCCTGTTCCTCAACCC CGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61877268..61877368 26863196 MeRIP-seq:(Medium) rs1407165975 Functional Loss DEL dbSNP153 32..33 33 - - - 56366 RMVar_ID_56366 Human_SNP_ID_469046439 m1A Human chr11 - 61877522 61877522 61877522 AAGTGGAAAATCTGGCGTACATGCTGGTGTGCATGCAGTGGGCGGTGAGTGGGGTTGCCCAGGAC AAGTGGAAAATCTGGCGTACATGCTGGTGTGCGTGCAGTGGGCGGTGAGTGGGGTTGCCCAGGAC T C FADS3 Ensembl:ENSG00000221968 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61877517..61877618 32194978 MeRIP-seq:(Medium) rs944741492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866525,Human_RBP_ID_9363646,Human_RBP_ID_18417097,Human_RBP_ID_18972061,Human_RBP_ID_21965741,Human_RBP_ID_22895033,Human_RBP_ID_23510521,Human_RBP_ID_27803488 Human_Splice_Rec_1246972,Human_Splice_Rec_1246973,Human_Splice_Rec_1247008,Human_Splice_Rec_1247009,Human_Splice_Rec_1247028,Human_Splice_Rec_1247029,Human_Splice_Rec_1247040,Human_Splice_Rec_1247041,Human_Splice_Rec_1247070,Human_Splice_Rec_1247071,Human_Splice_Rec_1247092,Human_Splice_Rec_1247093,Human_Splice_Rec_1247106,Human_Splice_Rec_1247107,Human_Splice_Rec_1247116 Human_miRNA_ID_2234932,Human_miRNA_ID_3029094 RMVar_hsa_circ_104890,RMVar_hsa_circ_126843,RMVar_hsa_circ_118092,RMVar_hsa_circ_20215,RMVar_hsa_circ_150113,RMVar_hsa_circ_84299,RMVar_hsa_circ_150111,RMVar_hsa_circ_150112,RMVar_hsa_circ_150110,RMVar_hsa_circ_90215,RMVar_hsa_circ_112220,RMVar_hsa_circ_150119,RMVar_hsa_circ_84969,RMVar_hsa_circ_150121,RMVar_hsa_circ_101951,RMVar_hsa_circ_150123,RMVar_hsa_circ_150124 56367 RMVar_ID_56367 Human_SNP_ID_469049979 m1A Human chr11 - 61891489 61891465 61891489 GTACGGCGGCCGCGGCGGCAGGGCGGGGCCGGAGCAGCGGGCGGCGGCGGAGGCGGCGCCCGGGA GTACGGCGGCCGCGGCGGCAGGGCGGGGCCGG________________________CGCCCGGGA GCCGCCTCCGCCGCCGCCCGCTGCT G FADS3 Ensembl:ENSG00000221968 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:61891284..61891523 26863196 MeRIP-seq:(Medium) rs1462425090 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_227363,Human_RBP_ID_750868,Human_RBP_ID_4184109 RMVar_hsa_circ_104890,RMVar_hsa_circ_150110 56368 RMVar_ID_56368 Human_SNP_ID_469051648 m1A Human chr11 + 61897710 61897710 61897710 GAAGGGAGGAAGCGGGGGAGGGGTCTTGACTCATCTTAACAAGGCTTTGGGGCAATTCTGTGCTA GAAGGGAGGAAGCGGGGGAGGGGTCTTGACTCCTCTTAACAAGGCTTTGGGGCAATTCTGTGCTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61897571..61897739 26863196 MeRIP-seq:(Medium) rs1048249907 Functional Loss SNV dbSNP153 33..33 33 - - - 56369 RMVar_ID_56369 Human_SNP_ID_469051655 m1A Human chr11 + 61897742 61897742 61897742 ATCTTAACAAGGCTTTGGGGCAATTCTGTGCTATGGAGGCCCTGCCAGCCCCTCCTAGTAGTCCA ATCTTAACAAGGCTTTGGGGCAATTCTGTGCTGTGGAGGCCCTGCCAGCCCCTCCTAGTAGTCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61897694..61897794 32194978 MeRIP-seq:(Medium) rs1187380261 Functional Loss SNV dbSNP153 33..33 33 - - - 56370 RMVar_ID_56370 Human_SNP_ID_469051797 m1A Human chr11 - 61898267 61898267 61898267 CTTCTTCCCCCAGGAGGCTTAGGGCGCGGCCCAGGCCTGAAGGGGAGCTCTGAGACAGAGCAAAC CTTCTTCCCCCAGGAGGCTTAGGGCGCGGCCCGGGCCTGAAGGGGAGCTCTGAGACAGAGCAAAC T C RAB3IL1 Ensembl:ENSG00000167994 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61897990..61898866 32194978 MeRIP-seq:(Medium) rs1363498645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1247150,Human_Splice_Rec_1247170,Human_Splice_Rec_1247186,Human_Splice_Rec_1247190,Human_Splice_Rec_1247192 RMVar_hsa_circ_103425,RMVar_hsa_circ_150127,RMVar_hsa_circ_86651,RMVar_hsa_circ_150126 56371 RMVar_ID_56371 Human_SNP_ID_469053017 m1A Human chr11 - 61902538 61902538 61902538 CCCCCGTGACCCATTTTGCTTTCCCCTAGCACATGTGCCCTGAGCGGGCTGACCCGCACCTGCCG CCCCCGTGACCCATTTTGCTTTCCCCTAGCACTTGTGCCCTGAGCGGGCTGACCCGCACCTGCCG T A RAB3IL1 Ensembl:ENSG00000167994 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61902491..61917458 32194978 MeRIP-seq:(Medium) rs527256903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1247146,Human_Splice_Rec_1247147,Human_Splice_Rec_1247166,Human_Splice_Rec_1247167,Human_Splice_Rec_1247182,Human_Splice_Rec_1247183,Human_Splice_Rec_1247194 RMVar_hsa_circ_226,RMVar_hsa_circ_103425,RMVar_hsa_circ_150127,RMVar_hsa_circ_86651,RMVar_hsa_circ_150126 56372 RMVar_ID_56372 Human_SNP_ID_469053018 m1A Human chr11 - 61902538 61902538 61902538 CCCCCGTGACCCATTTTGCTTTCCCCTAGCACATGTGCCCTGAGCGGGCTGACCCGCACCTGCCG CCCCCGTGACCCATTTTGCTTTCCCCTAGCACGTGTGCCCTGAGCGGGCTGACCCGCACCTGCCG T C RAB3IL1 Ensembl:ENSG00000167994 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61902491..61917458 32194978 MeRIP-seq:(Medium) rs527256903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1247146,Human_Splice_Rec_1247147,Human_Splice_Rec_1247166,Human_Splice_Rec_1247167,Human_Splice_Rec_1247182,Human_Splice_Rec_1247183,Human_Splice_Rec_1247194 RMVar_hsa_circ_226,RMVar_hsa_circ_103425,RMVar_hsa_circ_150127,RMVar_hsa_circ_86651,RMVar_hsa_circ_150126 56373 RMVar_ID_56373 Human_SNP_ID_469056789 m1A Human chr11 + 61917366 61917366 61917366 ACCGCGAGCGCGCGCGGACCTACCCGCTCCACATCCCGGCGCCTCGGGGCGCCCAGGCGTCCGTT ACCGCGAGCGCGCGCGGACCTACCCGCTCCACCTCCCGGCGCCTCGGGGCGCCCAGGCGTCCGTT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:61917358..61917558 26863196 MeRIP-seq:(Medium) rs1457150386 Functional Loss SNV dbSNP153 33..33 33 - - - 56374 RMVar_ID_56374 Human_SNP_ID_469056822 m1A Human chr11 - 61917448 61917448 61917448 GACAGGCGGTGGGGCGGCTCGGCCCCTGGCGGAGTCGGCGGCGGGCGGGGACGCGGCGCTGGGAG GACAGGCGGTGGGGCGGCTCGGCCCCTGGCGGCGTCGGCGGCGGGCGGGGACGCGGCGCTGGGAG T G RAB3IL1 Ensembl:ENSG00000167994 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:61907428..61917605 26863196 MeRIP-seq:(Medium) rs1254989068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1247133 56375 RMVar_ID_56375 Human_SNP_ID_469056823 m1A Human chr11 + 61917454 61917454 61917454 GCGCCGCGTCCCCGCCCGCCGCCGACTCCGCCAGGGGCCGAGCCGCCCCACCGCCTGTCAGCCCT GCGCCGCGTCCCCGCCCGCCGCCGACTCCGCCGGGGGCCGAGCCGCCCCACCGCCTGTCAGCCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61917362..61917555 26863196 MeRIP-seq:(Medium) rs1177253788 Functional Loss SNV dbSNP153 33..33 33 - - - 56376 RMVar_ID_56376 Human_SNP_ID_469068901 m1A Human chr11 + 61964782 61964782 61964782 CCAGGGTGTGCTTGTCAAAGAGATATTCCGCCAAGCCAGATTCGGGCGCTCCCATCTTGCGCAAG CCAGGGTGTGCTTGTCAAAGAGATATTCCGCCGAGCCAGATTCGGGCGCTCCCATCTTGCGCAAG A G BEST1 Ensembl:ENSG00000167995 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:61964673..61964824;chr11:61964690..61964809;chr11:61964678..61964818;chr11:61964678..61964816 26863196 MeRIP-seq:(Medium) rs193297277 Functional Loss SNV dbSNP153 33..33 33 - - - 56377 RMVar_ID_56377 Human_SNP_ID_469068904 m1A Human chr11 - 61964790 61964790 61964790 GTGACCAACTTGCGCAAGATGGGAGCGCCCGAATCTGGCTTGGCGGAATATCTCTTTGACAAGCA GTGACCAACTTGCGCAAGATGGGAGCGCCCGAGTCTGGCTTGGCGGAATATCTCTTTGACAAGCA T C FTH1 Ensembl:ENSG00000167996 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61964751..61964825 32194978 MeRIP-seq:(Medium) rs374812527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32542,Human_RBP_ID_398651,Human_RBP_ID_751528,Human_RBP_ID_987590,Human_RBP_ID_5138897,Human_RBP_ID_17232548,Human_RBP_ID_17348896,Human_RBP_ID_17465267,Human_RBP_ID_17797948,Human_RBP_ID_22432961,Human_RBP_ID_23510538,Human_RBP_ID_26803599,Human_RBP_ID_27412832,Human_RBP_ID_27556945 56378 RMVar_ID_56378 Human_SNP_ID_469068930 m1A Human chr11 - 61964838 61964838 61964838 CATTACCTGAATGAGCAGGTGAAAGCCATCAAAGAATTGGGTGACCACGTGACCAACTTGCGCAA CATTACCTGAATGAGCAGGTGAAAGCCATCAAGGAATTGGGTGACCACGTGACCAACTTGCGCAA T C FTH1 Ensembl:ENSG00000167996 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1439051422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17805604 Human_Splice_Rec_1247316,Human_Splice_Rec_1247322,Human_Splice_Rec_1247328,Human_Splice_Rec_1247334,Human_Splice_Rec_1247340,Human_Splice_Rec_1247346,Human_Splice_Rec_1247354 56379 RMVar_ID_56379 Human_SNP_ID_469068992 m1A Human chr11 - 61965003 61965003 61965003 GTCACTACTGGAACTGCACAAACTGGCCACTGACAAAAATGACCCCCATGTGAGTATTGGAACCC GTCACTACTGGAACTGCACAAACTGGCCACTGCCAAAAATGACCCCCATGTGAGTATTGGAACCC T G FTH1 Ensembl:ENSG00000167996 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs754709149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362324,Human_RBP_ID_17234102,Human_RBP_ID_17350163,Human_RBP_ID_17466959,Human_RBP_ID_18456385,Human_RBP_ID_22435324 Human_Splice_Rec_1247315,Human_Splice_Rec_1247321,Human_Splice_Rec_1247327,Human_Splice_Rec_1247333,Human_Splice_Rec_1247339,Human_Splice_Rec_1247345,Human_Splice_Rec_1247353 RMVar_hsa_circ_81481,RMVar_hsa_circ_150131 56380 RMVar_ID_56380 Human_SNP_ID_469069015 m1A Human chr11 + 61965077 61965077 61965077 TTTTTTTCCAAATGTAATGCACACTCCATTGCATTCAGCCCGCTCTCCCAGTCATCACAGTCTGG TTTTTTTCCAAATGTAATGCACACTCCATTGCGTTCAGCCCGCTCTCCCAGTCATCACAGTCTGG A G BEST1 Ensembl:ENSG00000167995 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61965016..61965127 26863196 MeRIP-seq:(Medium) rs770111345 Functional Loss SNV dbSNP153 33..33 33 - - - 56381 RMVar_ID_56381 Human_SNP_ID_469069716 m1A Human chr11 - 61967460 61967454 61967460 GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCCACCGCCGCCGCCGCCGCCTCTCCTTAGTCGCCG GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCC______GCCGCCGCCGCCTCTCCTTAGTCGCCG CGGCGGT C FTH1 Ensembl:ENSG00000167996 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chr11:61967301..61967660;chr11:61967362..61967625 26863410 MeRIP-seq:(Medium) rs1247251515 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_227905,Human_RBP_ID_398663,Human_RBP_ID_752389,Human_RBP_ID_4165562,Human_RBP_ID_9321435,Human_RBP_ID_17234114,Human_RBP_ID_17350168,Human_RBP_ID_17465274,Human_RBP_ID_22532282,Human_RBP_ID_24460355,Human_RBP_ID_26404799,Human_RBP_ID_27203063 Human_Splice_Rec_1247335 56382 RMVar_ID_56382 Human_SNP_ID_469069722 m1A Human chr11 - 61967460 61967457 61967460 GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCCACCGCCGCCGCCGCCGCCTCTCCTTAGTCGCCG GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCC___GCCGCCGCCGCCGCCTCTCCTTAGTCGCCG CGGT C FTH1 Ensembl:ENSG00000167996 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chr11:61967301..61967660;chr11:61967362..61967625 26863410 MeRIP-seq:(Medium) rs1386409381 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_227905,Human_RBP_ID_398663,Human_RBP_ID_752389,Human_RBP_ID_4165562,Human_RBP_ID_9321435,Human_RBP_ID_17234114,Human_RBP_ID_17350168,Human_RBP_ID_17465274,Human_RBP_ID_22532282,Human_RBP_ID_24460355,Human_RBP_ID_26404799,Human_RBP_ID_27203063 Human_Splice_Rec_1247335 56383 RMVar_ID_56383 Human_SNP_ID_469069725 m1A Human chr11 - 61967460 61967460 61967460 GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCCACCGCCGCCGCCGCCGCCTCTCCTTAGTCGCCG GGCCCCCGCCGCCGCTCCAGCGCCGCGCAGCCGCCGCCGCCGCCGCCGCCTCTCCTTAGTCGCCG T C FTH1 Ensembl:ENSG00000167996 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chr11:61967301..61967660;chr11:61967362..61967625 26863410 MeRIP-seq:(Medium) rs1436389011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227905,Human_RBP_ID_398663,Human_RBP_ID_752389,Human_RBP_ID_4165562,Human_RBP_ID_9321435,Human_RBP_ID_17234114,Human_RBP_ID_17350168,Human_RBP_ID_17465274,Human_RBP_ID_22532282,Human_RBP_ID_24460355,Human_RBP_ID_26404799,Human_RBP_ID_27203063 Human_Splice_Rec_1247335 56384 RMVar_ID_56384 Human_SNP_ID_469069758 m1A Human chr11 - 61967515 61967515 61967515 GCCGCCCATAGCCAGCCCTCCGTCACCTCTTCACCGCACCCTCGGACTGCCCCAAGGCCCCCGCC GCCGCCCATAGCCAGCCCTCCGTCACCTCTTCTCCGCACCCTCGGACTGCCCCAAGGCCCCCGCC T A FTH1 Ensembl:ENSG00000167996 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:61967346..61967650 26863196 MeRIP-seq:(Medium) rs763229761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227905,Human_RBP_ID_398663,Human_RBP_ID_752389,Human_RBP_ID_5460492,Human_RBP_ID_9321435,Human_RBP_ID_17234117,Human_RBP_ID_17350173,Human_RBP_ID_17465275,Human_RBP_ID_18609494,Human_RBP_ID_18933558,Human_RBP_ID_22532282,Human_RBP_ID_24460357,Human_RBP_ID_26404803,Human_RBP_ID_27412839 56385 RMVar_ID_56385 Human_SNP_ID_469069788 m1A Human chr11 + 61967562 61967562 61967562 GGGCTGGCTATGGGCGGCCGGCCGGGGTGGGGAACGAGCGCCGGGTTCCGTCCAAGCACTGTTGA GGGCTGGCTATGGGCGGCCGGCCGGGGTGGGGGACGAGCGCCGGGTTCCGTCCAAGCACTGTTGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr11:61967251..61967625;chr11:61967120..61967650;chr11:61967301..61967650;chr11:61967323..61967625 26863196 MeRIP-seq:(Medium) rs750898501 Functional Loss SNV dbSNP153 33..33 33 - - - 56386 RMVar_ID_56386 Human_SNP_ID_469069949 m1A Human chr11 + 61967876 61967876 61967876 GTCTCTGTGCCCGTTTAGTGGAGTTGGAGGGAAGCTGCGAGGAGGCGCAGGAAGTCCACCTCAGA GTCTCTGTGCCCGTTTAGTGGAGTTGGAGGGATGCTGCGAGGAGGCGCAGGAAGTCCACCTCAGA A T AP003733.3 Ensembl:ENSG00000279491 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:61967843..61968143;chr11:61967843..61968093 26863196 MeRIP-seq:(Medium) rs1310693598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5552297 56387 RMVar_ID_56387 Human_SNP_ID_469070155 m1A Human chr11 + 61968338 61968337 61968338 GCTGGGCGGGCCGGGTTTCCCTAGGGATGGGGACCGCCTCCCCGGGGAGTCGTGGGGGTGAGCCA GCTGGGCGGGCCGGGTTTCCCTAGGGATGGGG_CCGCCTCCCCGGGGAGTCGTGGGGGTGAGCCA GA G AP003733.3 Ensembl:ENSG00000279491 Other exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:61968292..61968393 26863196 MeRIP-seq:(Medium) rs1455756436 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3389259,Human_RBP_ID_5644336,Human_RBP_ID_8177090,Human_RBP_ID_22035678 56388 RMVar_ID_56388 Human_SNP_ID_469107312 m1A Human chr11 + 62124134 62124134 62124134 CTTACCTAGGGATACCACCGGACTTGGATCGGAGCAGCCTTCAGGGGACGTGGCGCAGTCGAGTG CTTACCTAGGGATACCACCGGACTTGGATCGGGGCAGCCTTCAGGGGACGTGGCGCAGTCGAGTG A G INCENP Ensembl:ENSG00000149503 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62124083..62124211 26863196 MeRIP-seq:(Medium) rs777102920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780465,Human_RBP_ID_3376946,Human_RBP_ID_4184931,Human_RBP_ID_5460493,Human_RBP_ID_6081944,Human_RBP_ID_8353681,Human_RBP_ID_8770251,Human_RBP_ID_9321437,Human_RBP_ID_11654800,Human_RBP_ID_17797957,Human_RBP_ID_18416561,Human_RBP_ID_18609501,Human_RBP_ID_23124524 Human_Splice_Rec_1247373,Human_Splice_Rec_1247407,Human_Splice_Rec_1247415 56389 RMVar_ID_56389 Human_SNP_ID_469108341 m1A Human chr11 + 62128275 62128275 62128275 AATAAGGACTTGGTGTGGCTTGAGGAAATCCAAGAGGAGGCCGAGCGCATGTTCACCAGGTGAAG AATAAGGACTTGGTGTGGCTTGAGGAAATCCACGAGGAGGCCGAGCGCATGTTCACCAGGTGAAG A C INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62124071..62128776 32194978 MeRIP-seq:(Medium) rs766073816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_869502,Human_RBP_ID_9362326,Human_RBP_ID_26318410,Human_RBP_ID_26804738 Human_Splice_Rec_1247369,Human_Splice_Rec_1247375,Human_Splice_Rec_1247409,Human_Splice_Rec_1247417 RMVar_hsa_circ_14518,RMVar_hsa_circ_300008,RMVar_hsa_circ_100556,RMVar_hsa_circ_150133,RMVar_hsa_circ_150134 56390 RMVar_ID_56390 Human_SNP_ID_469108866 m1A Human chr11 - 62130049 62130049 62130049 TGGGTGACATGCTGCTCAGCATTCTGGCGCTCACTGATGCCGATCTCCACCACAGGCACCAGCTG TGGGTGACATGCTGCTCAGCATTCTGGCGCTCGCTGATGCCGATCTCCACCACAGGCACCAGCTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:62130001..62130175 26863196 MeRIP-seq:(Medium) rs752382818 Functional Loss SNV dbSNP153 33..33 33 - - - 56391 RMVar_ID_56391 Human_SNP_ID_469108877 m1A Human chr11 - 62130087 62130087 62130087 GGGACAGAGTGCGGGGCAGAGGCTCGGTGGACATGAGCTGGGTGACATGCTGCTCAGCATTCTGG GGGACAGAGTGCGGGGCAGAGGCTCGGTGGACTTGAGCTGGGTGACATGCTGCTCAGCATTCTGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62130038..62130174 26863196 MeRIP-seq:(Medium) rs144643595 Functional Loss SNV dbSNP153 33..33 33 - - - 56392 RMVar_ID_56392 Human_SNP_ID_469108878 m1A Human chr11 - 62130087 62130087 62130087 GGGACAGAGTGCGGGGCAGAGGCTCGGTGGACATGAGCTGGGTGACATGCTGCTCAGCATTCTGG GGGACAGAGTGCGGGGCAGAGGCTCGGTGGACGTGAGCTGGGTGACATGCTGCTCAGCATTCTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62130038..62130174 26863196 MeRIP-seq:(Medium) rs144643595 Functional Loss SNV dbSNP153 33..33 33 - - - 56393 RMVar_ID_56393 Human_SNP_ID_469108884 m1A Human chr11 - 62130102 62130102 62130102 CTGAAGCTGGAGTCGGGGACAGAGTGCGGGGCAGAGGCTCGGTGGACATGAGCTGGGTGACATGC CTGAAGCTGGAGTCGGGGACAGAGTGCGGGGCGGAGGCTCGGTGGACATGAGCTGGGTGACATGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62130001..62130225 26863196 MeRIP-seq:(Medium) rs909572833 Functional Loss SNV dbSNP153 33..33 33 - - - 56394 RMVar_ID_56394 Human_SNP_ID_469108906 m1A Human chr11 - 62130149 62130149 62130149 TGATTCCTCATCTGATGTCGGGATGCCCTGGGAGGTTGGAGCTGTGGCTGAAGCTGGAGTCGGGG TGATTCCTCATCTGATGTCGGGATGCCCTGGGGGGTTGGAGCTGTGGCTGAAGCTGGAGTCGGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62130126..62130150 26863196 MeRIP-seq:(Medium) rs763857838 Functional Loss SNV dbSNP153 33..33 33 - - - 56395 RMVar_ID_56395 Human_SNP_ID_469111131 m1A Human chr11 + 62138943 62138943 62138943 CTCGTGGCCCCACAATGACACGGAGATTGCCAACAGCACACCCAACCCGAAGCCTGCAGCCAGCA CTCGTGGCCCCACAATGACACGGAGATTGCCAGCAGCACACCCAACCCGAAGCCTGCAGCCAGCA A G INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:62138787..62141550;chr11:62138777..62139053 26863196 MeRIP-seq:(Medium) rs914170960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32364,Human_RBP_ID_1780478,Human_RBP_ID_9363654 Human_Splice_Rec_1247384,Human_Splice_Rec_1247385,Human_Splice_Rec_1247426,Human_Splice_Rec_1247427,Human_Splice_Rec_1247456,Human_Splice_Rec_1247457 RMVar_hsa_circ_150136,RMVar_hsa_circ_326870 56396 RMVar_ID_56396 Human_SNP_ID_469111608 m1A Human chr11 - 62140661 62140661 62140661 GCGGGCGGCGGCATCACAGGGCAGCCCGCCACAGCCCAGCCACACCCCATCAAAAGTCACCCCGG GCGGGCGGCGGCATCACAGGGCAGCCCGCCACGGCCCAGCCACACCCCATCAAAAGTCACCCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62140656..62140825 26863196 MeRIP-seq:(Medium) rs1349171027 Functional Loss SNV dbSNP153 33..33 33 - - - 56397 RMVar_ID_56397 Human_SNP_ID_469111790 m1A Human chr11 + 62141043 62141043 62141043 TAAGCGCAACACTCCCCTGCGCATGGACCCCAAGGTGAGGGGCCTGTGCCCAGGCCGGGCTTTGT TAAGCGCAACACTCCCCTGCGCATGGACCCCATGGTGAGGGGCCTGTGCCCAGGCCGGGCTTTGT A T INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:62140668..62141083;chr11:62140659..62141050 26863196 MeRIP-seq:(Medium) rs1160305249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773515,Human_RBP_ID_19049517 Human_Splice_Rec_1247391,Human_Splice_Rec_1247433,Human_Splice_Rec_1247463 RMVar_hsa_circ_14089,RMVar_hsa_circ_150137,RMVar_hsa_circ_122084,RMVar_hsa_circ_334500 56398 RMVar_ID_56398 Human_SNP_ID_469112889 m1A Human chr11 + 62145234 62145234 62145234 GGCCCGCGAGCGGGTGGAGCAGATGAAGGAGGAGAAGAAGAAGCAGATTGAGCAGAAGTTTGCTC GGCCCGCGAGCGGGTGGAGCAGATGAAGGAGGGGAAGAAGAAGCAGATTGAGCAGAAGTTTGCTC A G INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62145058..62145331 26863196 MeRIP-seq:(Medium) rs1451936101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30911,Human_RBP_ID_1780479,Human_RBP_ID_22895674,Human_RBP_ID_24542350,Human_RBP_ID_26318421 Human_Splice_Rec_1247394,Human_Splice_Rec_1247395,Human_Splice_Rec_1247438,Human_Splice_Rec_1247439 RMVar_hsa_circ_35079,RMVar_hsa_circ_150138,RMVar_hsa_circ_86131,RMVar_hsa_circ_150139,RMVar_hsa_circ_377631,RMVar_hsa_circ_150140,RMVar_hsa_circ_378858 56399 RMVar_ID_56399 Human_SNP_ID_469113011 m1A Human chr11 + 62145649 62145649 62145649 TGGGCTCTGCAGGCCAAGGAGGAGCGGCTGGCAGAGGAGAAGGCCAAGAAAAAGGCGGCGGCCAA TGGGCTCTGCAGGCCAAGGAGGAGCGGCTGGCGGAGGAGAAGGCCAAGAAAAAGGCGGCGGCCAA A G INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:62145626..62145775 26863196 MeRIP-seq:(Medium) rs1554979989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30912,Human_RBP_ID_193355,Human_RBP_ID_1461977,Human_RBP_ID_22571086,Human_RBP_ID_24542353,Human_RBP_ID_26319877,Human_RBP_ID_27804503 Human_Splice_Rec_1247396,Human_Splice_Rec_1247440 RMVar_hsa_circ_150138,RMVar_hsa_circ_86131,RMVar_hsa_circ_150139,RMVar_hsa_circ_377631,RMVar_hsa_circ_150140,RMVar_hsa_circ_378858 56400 RMVar_ID_56400 Human_SNP_ID_469113021 m1A Human chr11 - 62145687 62145687 62145687 CTTCCTGCTTCCTGCGTGCTTCCACCTCCTCCATCTTCTTGGCCGCCGCCTTTTTCTTGGCCTTC CTTCCTGCTTCCTGCGTGCTTCCACCTCCTCCGTCTTCTTGGCCGCCGCCTTTTTCTTGGCCTTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:62145548..62145814 26863196 MeRIP-seq:(Medium) rs1479873144 Functional Loss SNV dbSNP153 33..33 33 - - - 56401 RMVar_ID_56401 Human_SNP_ID_469113330 m1A Human chr11 + 62146753 62146753 62146753 CTGCGGAAGGCGGCCGAGGCTAAGCGGCTGGCAGAGCAGCGGGAGCAGGAGCGGCGGGAGCAGGA CTGCGGAAGGCGGCCGAGGCTAAGCGGCTGGCGGAGCAGCGGGAGCAGGAGCGGCGGGAGCAGGA A G INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62144953..62148825 26863196 MeRIP-seq:(Medium) rs1565101419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24542356 Human_Splice_Rec_1247398,Human_Splice_Rec_1247442 RMVar_hsa_circ_150138,RMVar_hsa_circ_86131 56402 RMVar_ID_56402 Human_SNP_ID_469114352 m1A Human chr11 + 62150151 62150151 62150151 CCCAGATAACTACGGGATGGATCTGAATAGCGACGACTCCACCGATGATGAGGCCCATCCCCGGA CCCAGATAACTACGGGATGGATCTGAATAGCGCCGACTCCACCGATGATGAGGCCCATCCCCGGA A C INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62150038..62150228 26863196 MeRIP-seq:(Medium) rs1455310976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780480,Human_RBP_ID_6082000,Human_RBP_ID_11655319 Human_Splice_Rec_1247404,Human_Splice_Rec_1247405,Human_Splice_Rec_1247448,Human_Splice_Rec_1247449 56403 RMVar_ID_56403 Human_SNP_ID_469160421 m1A Human chr11 - 62337517 62337517 62337517 CGAGACCTCAAGCTGGGTCGAGCCAGCCCCGCAGCCGCCCGGTACCGCCGCTCCCCGACGCCGGC CGAGACCTCAAGCTGGGTCGAGCCAGCCCCGCTGCCGCCCGGTACCGCCGCTCCCCGACGCCGGC T A AP003306.2 Ensembl:ENSG00000255118 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:62337451..62337599;chr11:62337451..62337605 26863196 MeRIP-seq:(Medium) rs894088585 Functional Loss SNV dbSNP153 33..33 33 - - - 56404 RMVar_ID_56404 Human_SNP_ID_469165122 m1A Human chr11 + 62356375 62356375 62356375 ACACAAATGGTGAGGTTGAAATGGATGCTAGTATCATGGATGGAAAAGACCTGTCTGCAGGAGCA ACACAAATGGTGAGGTTGAAATGGATGCTAGTGTCATGGATGGAAAAGACCTGTCTGCAGGAGCA A G ASRGL1 Ensembl:ENSG00000162174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62356281..62356384 32194978 MeRIP-seq:(Medium) rs1443226313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23510672 Human_Splice_Rec_1247498,Human_Splice_Rec_1247499,Human_Splice_Rec_1247516,Human_Splice_Rec_1247517,Human_Splice_Rec_1247546,Human_Splice_Rec_1247547,Human_Splice_Rec_1247552,Human_Splice_Rec_1247553 RMVar_hsa_circ_150142,RMVar_hsa_circ_322633 56405 RMVar_ID_56405 Human_SNP_ID_469174276 m1A Human chr11 - 62389239 62389239 62389239 GAGGCATCCCTTGGTCCTACCTAGACACGGTGAGTCCCCAACGCGGCCGACCATTTTATTAACGA GAGGCATCCCTTGGTCCTACCTAGACACGGTGGGTCCCCAACGCGGCCGACCATTTTATTAACGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62389189..62389290 32194978 MeRIP-seq:(Medium) rs1162728459 Functional Loss SNV dbSNP153 33..33 33 - - - 56406 RMVar_ID_56406 Human_SNP_ID_469175275 m1A Human chr11 + 62393097 62393097 62393097 TATAGTGAGTAATGGGGCTCAGGGCCTCTCCAACAACAGAGAGGAGCTGATGCTGTAGGGCTGAC TATAGTGAGTAATGGGGCTCAGGGCCTCTCCAGCAACAGAGAGGAGCTGATGCTGTAGGGCTGAC A G ASRGL1 Ensembl:ENSG00000162174 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62393012..62393113 32194978 MeRIP-seq:(Medium) rs1181766064 Functional Loss SNV dbSNP153 33..33 33 - - - 56407 RMVar_ID_56407 Human_SNP_ID_469175321 m1A Human chr11 - 62393261 62393261 62393261 CATTTCCAGTGTAATGAGAGATAAAGAGGAATACTGCCCACCGAGGAAATGACTTTCTTCACCAT CATTTCCAGTGTAATGAGAGATAAAGAGGAATGCTGCCCACCGAGGAAATGACTTTCTTCACCAT T C AP003064.1 Ensembl:ENSG00000255126 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62393212..62393312 32194978 MeRIP-seq:(Medium) rs1345869694 Functional Loss SNV dbSNP153 33..33 33 - - - 56408 RMVar_ID_56408 Human_SNP_ID_469207028 m1A Human chr11 - 62517327 62517314 62517328 AGCAGAGGCCAGCATCCAAGCTGGTGCTGGAGACGGCGAGTGGGAAGAGTCTGAAGTCAAACTGA AGCAGAGGCCAGCATCCAAGCTGGTGCTGGA______________AGAGTCTGAAGTCAAACTGA TTCCCACTCGCCGTC T AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62517226..62517450 32194978 MeRIP-seq:(Medium) rs756647537 Functional Loss DEL dbSNP153 32..45 33 - - - Human_RBP_ID_8773519,Human_RBP_ID_22569260,Human_RBP_ID_22708750 RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_78465,RMVar_hsa_circ_112782,RMVar_hsa_circ_121290,RMVar_hsa_circ_150145,RMVar_hsa_circ_111908,RMVar_hsa_circ_150146,RMVar_hsa_circ_150148,RMVar_hsa_circ_150149,RMVar_hsa_circ_150147 56409 RMVar_ID_56409 Human_SNP_ID_469207041 m1A Human chr11 - 62517327 62517327 62517327 AGCAGAGGCCAGCATCCAAGCTGGTGCTGGAGACGGCGAGTGGGAAGAGTCTGAAGTCAAACTGA AGCAGAGGCCAGCATCCAAGCTGGTGCTGGAGGCGGCGAGTGGGAAGAGTCTGAAGTCAAACTGA T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62517226..62517450 32194978 MeRIP-seq:(Medium) rs781168176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773519,Human_RBP_ID_22569260,Human_RBP_ID_22708750 RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_78465,RMVar_hsa_circ_112782,RMVar_hsa_circ_121290,RMVar_hsa_circ_150145,RMVar_hsa_circ_111908,RMVar_hsa_circ_150146,RMVar_hsa_circ_150148,RMVar_hsa_circ_150149,RMVar_hsa_circ_150147 56410 RMVar_ID_56410 Human_SNP_ID_469211183 m1A Human chr11 + 62527519 62527519 62527519 GGGGGTCTTGAAGTGCATCTCAGGCATCTTAAACTTGGGGCCCTTCAGCTTCCCTTCTGGACCTT GGGGGTCTTGAAGTGCATCTCAGGCATCTTAAGCTTGGGGCCCTTCAGCTTCCCTTCTGGACCTT A G NONHSAG008515.2,NONHSAG008515.2:2,NONHSAG008515.2:3,NONHSAG008515.2:4,NONHSAG008515.2:5 RNACentral:URS00009BDEDD,RNACentral:URS00008C0DAB,RNACentral:URS00008C0C25,RNACentral:URS00009C0D48,RNACentral:URS00008C1162 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62527501..62527575 32194978 MeRIP-seq:(Medium) rs138917652 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 56411 RMVar_ID_56411 Human_SNP_ID_469212167 m1A Human chr11 - 62529868 62529868 62529868 GGCACCTGAAGATGCCCAAGGTAAAAATGCCCAAGTTCAGCATGCCTGGCTTTAAAGGAGAGGGC GGCACCTGAAGATGCCCAAGGTAAAAATGCCCGAGTTCAGCATGCCTGGCTTTAAAGGAGAGGGC T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62529676..62529975 32194978 MeRIP-seq:(Medium) rs1431680951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108816,Human_RBP_ID_8229378,Human_RBP_ID_9443935,Human_RBP_ID_17668656,Human_RBP_ID_22521701,Human_RBP_ID_26768120,Human_RBP_ID_27571716 RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_78465,RMVar_hsa_circ_112782,RMVar_hsa_circ_121290,RMVar_hsa_circ_150145,RMVar_hsa_circ_111908,RMVar_hsa_circ_150146,RMVar_hsa_circ_150148,RMVar_hsa_circ_150149,RMVar_hsa_circ_150147 56412 RMVar_ID_56412 Human_SNP_ID_469213047 m1A Human chr11 + 62532001 62532001 62532001 GGGGACTTTGATGTTCATCTCAGGCATCTTAAACTTGGGCCCTTTCAATTTCCCTTCTGGTTCCT GGGGACTTTGATGTTCATCTCAGGCATCTTAAGCTTGGGCCCTTTCAATTTCCCTTCTGGTTCCT A G NONHSAG008515.2,NONHSAG008515.2:2,NONHSAG008515.2:3,NONHSAG008515.2:4 RNACentral:URS00009BDEDD,RNACentral:URS00008C0DAB,RNACentral:URS00008C0C25,RNACentral:URS00009C0D48 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62531901..62532300 32194978 MeRIP-seq:(Medium) rs1270280799 Functional Loss SNV dbSNP153 33..33 33 - - - 56413 RMVar_ID_56413 Human_SNP_ID_469213172 m1A Human chr11 - 62532282 62532282 62532282 TGTAGATTTGCACGTGAAAGGTACAAAGGTGAAGGGAGAGTATGATGTAACTGTACCAAAGCTGG TGTAGATTTGCACGTGAAAGGTACAAAGGTGAGGGGAGAGTATGATGTAACTGTACCAAAGCTGG T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62532231..62532347 26863196 MeRIP-seq:(Medium) rs145845956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30329,Human_RBP_ID_108818,Human_RBP_ID_17682231,Human_RBP_ID_17805145 Human_miRNA_ID_2094344,Human_miRNA_ID_2718409,Human_miRNA_ID_2922505 RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_78465,RMVar_hsa_circ_112782,RMVar_hsa_circ_121290,RMVar_hsa_circ_150145,RMVar_hsa_circ_111908,RMVar_hsa_circ_150146,RMVar_hsa_circ_150148,RMVar_hsa_circ_150149,RMVar_hsa_circ_150147 56414 RMVar_ID_56414 Human_SNP_ID_469213223 m1A Human chr11 + 62532400 62532400 62532400 GGGGCCTTTAAGTTTTCCCCCCAGACCCTCCAAGTTGACATCTGGGGCTTCCACATTGACCTTGG GGGGCCTTTAAGTTTTCCCCCCAGACCCTCCAGGTTGACATCTGGGGCTTCCACATTGACCTTGG A G NONHSAG008515.2,NONHSAG008515.2:2,NONHSAG008515.2:3,NONHSAG008515.2:4 RNACentral:URS00009BDEDD,RNACentral:URS00008C0DAB,RNACentral:URS00008C0C25,RNACentral:URS00009C0D48 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62532351..62532925 32194978 MeRIP-seq:(Medium) rs538684241 Functional Loss SNV dbSNP153 33..33 33 - - - 56415 RMVar_ID_56415 Human_SNP_ID_469213636 m1A Human chr11 - 62533527 62533527 62533527 TAGGGCAGTAGAGGTACAGGGCCCATCTCTGGAGAGTGGTGATCATGGCAAAATTAAATTTCCCA TAGGGCAGTAGAGGTACAGGGCCCATCTCTGGGGAGTGGTGATCATGGCAAAATTAAATTTCCCA T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62533476..62534025 32194978 MeRIP-seq:(Medium) rs959131943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30340,Human_RBP_ID_5313624,Human_RBP_ID_5520753,Human_RBP_ID_8770520,Human_RBP_ID_9275754,Human_RBP_ID_17648767,Human_RBP_ID_18544150,Human_RBP_ID_19028316,Human_RBP_ID_22034511,Human_RBP_ID_22426104,Human_RBP_ID_22435353,Human_RBP_ID_22521714,Human_RBP_ID_22708840,Human_RBP_ID_22790843,Human_RBP_ID_23267705,Human_RBP_ID_26318504,Human_RBP_ID_26767933,Human_RBP_ID_27571881 Human_miRNA_ID_2171769,Human_miRNA_ID_2825094,Human_miRNA_ID_2859063 RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_78465,RMVar_hsa_circ_112782,RMVar_hsa_circ_121290,RMVar_hsa_circ_150145,RMVar_hsa_circ_111908,RMVar_hsa_circ_150146,RMVar_hsa_circ_150148,RMVar_hsa_circ_150149,RMVar_hsa_circ_150147 56416 RMVar_ID_56416 Human_SNP_ID_469216215 m1A Human chr11 + 62543233 62543233 62543233 TCTGGACACAAACTGCGCGTGCGGACATGTCCAGGACCGAGAAACTCACTTCAGTCCTTACCTAC TCTGGACACAAACTGCGCGTGCGGACATGTCCCGGACCGAGAAACTCACTTCAGTCCTTACCTAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62543230..62543332 32194978 MeRIP-seq:(Medium) rs1462885800 Functional Loss SNV dbSNP153 33..33 33 - - - 56417 RMVar_ID_56417 Human_SNP_ID_469216216 m1A Human chr11 + 62543233 62543233 62543233 TCTGGACACAAACTGCGCGTGCGGACATGTCCAGGACCGAGAAACTCACTTCAGTCCTTACCTAC TCTGGACACAAACTGCGCGTGCGGACATGTCCGGGACCGAGAAACTCACTTCAGTCCTTACCTAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62543230..62543332 32194978 MeRIP-seq:(Medium) rs1462885800 Functional Loss SNV dbSNP153 33..33 33 - - - 56418 RMVar_ID_56418 Human_SNP_ID_469216530 m1A Human chr11 - 62544409 62544407 62544410 GGACACTGGTCAGAGAACAGGGACACATGGGGAGCCACATAAGTCATGCGGGCTGATATGGAGGC GGACACTGGTCAGAGAACAGGGACACATGGG___CCACATAAGTCATGCGGGCTGATATGGAGGC GCTC G AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62544408..62544542 26863196 MeRIP-seq:(Medium) rs1398865655 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_398814,Human_RBP_ID_11655934 56419 RMVar_ID_56419 Human_SNP_ID_469216532 m1A Human chr11 - 62544409 62544409 62544409 GGACACTGGTCAGAGAACAGGGACACATGGGGAGCCACATAAGTCATGCGGGCTGATATGGAGGC GGACACTGGTCAGAGAACAGGGACACATGGGGTGCCACATAAGTCATGCGGGCTGATATGGAGGC T A AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62544408..62544542 26863196 MeRIP-seq:(Medium) rs1369470901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398814,Human_RBP_ID_11655934 56420 RMVar_ID_56420 Human_SNP_ID_469216533 m1A Human chr11 + 62544414 62544414 62544414 CATATCAGCCCGCATGACTTATGTGGCTCCCCATGTGTCCCTGTTCTCTGACCAGTGTCCCTGTG CATATCAGCCCGCATGACTTATGTGGCTCCCCTTGTGTCCCTGTTCTCTGACCAGTGTCCCTGTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62544411..62544521 26863196 MeRIP-seq:(Medium) rs528991986 Functional Loss SNV dbSNP153 33..33 33 - - - 56421 RMVar_ID_56421 Human_SNP_ID_469216829 m1A Human chr11 - 62545527 62545527 62545527 GCAGAGCTGTGTTATGTAAGGCTTTCCCATGCAAGGGGAGGGGGTGTGTGTGTGCAGTGTGCGAG GCAGAGCTGTGTTATGTAAGGCTTTCCCATGCGAGGGGAGGGGGTGTGTGTGTGCAGTGTGCGAG T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62545521..62545738 26863196 MeRIP-seq:(Medium) rs567287784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385092,Human_RBP_ID_5138581,Human_RBP_ID_8064199,Human_RBP_ID_8229243 56422 RMVar_ID_56422 Human_SNP_ID_469217005 m1A Human chr11 + 62546170 62546170 62546170 ACGACTCGGGACGCGGTTAGGGGCAGAGGTGCAGGGAGCGCGGAAGGACAGCCGAGGGGGCGCAC ACGACTCGGGACGCGGTTAGGGGCAGAGGTGCGGGGAGCGCGGAAGGACAGCCGAGGGGGCGCAC A G AP001363.2 Ensembl:ENSG00000257058 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62546168..62546274 26863196 MeRIP-seq:(Medium) rs767778681 Functional Loss SNV dbSNP153 33..33 33 - - - 56423 RMVar_ID_56423 Human_SNP_ID_469217161 m1A Human chr11 - 62546657 62546657 62546657 TATGGCCGTGCCCTGGGGCTGAGCCCTCAGGTAGGGGCGCCAGGCGCACCGTGGCGCCATCGGGG TATGGCCGTGCCCTGGGGCTGAGCCCTCAGGTGGGGGCGCCAGGCGCACCGTGGCGCCATCGGGG T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62546650..62546789 26863196 MeRIP-seq:(Medium) rs1162427388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184940,Human_RBP_ID_8773602 56424 RMVar_ID_56424 Human_SNP_ID_469219400 m1A Human chr11 - 62556001 62556001 62556001 AAACTGGAGAAGGGGTCGGGGCTCAGGGCTGCAGTTGACTCAGATAAAATCTTTACAGAGCCTGG AAACTGGAGAAGGGGTCGGGGCTCAGGGCTGCTGTTGACTCAGATAAAATCTTTACAGAGCCTGG T A AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62555995..62556062 26863196 MeRIP-seq:(Medium) rs973275799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6082278,Human_RBP_ID_11656121,Human_RBP_ID_23510810 56425 RMVar_ID_56425 Human_SNP_ID_469220396 m1A Human chr11 - 62559777 62559777 62559777 AGTCATACACATGGCGGAAACTGGATCCTGGCAGCGAGGAGACCCAGACGCTGGTTCGAGAGTAC AGTCATACACATGGCGGAAACTGGATCCTGGCGGCGAGGAGACCCAGACGCTGGTTCGAGAGTAC T C AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:62559657..62559811;chr11:62559673..62559797;chr11:62559726..62559812 26863196 MeRIP-seq:(Medium) rs1467091858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227369,Human_RBP_ID_398831,Human_RBP_ID_750876,Human_RBP_ID_808015,Human_RBP_ID_869095,Human_RBP_ID_987643,Human_RBP_ID_1458151,Human_RBP_ID_1780528,Human_RBP_ID_5170218,Human_RBP_ID_5549484,Human_RBP_ID_6082321,Human_RBP_ID_8246405,Human_RBP_ID_8353829,Human_RBP_ID_9004593,Human_RBP_ID_11656280,Human_RBP_ID_17232563,Human_RBP_ID_17798099,Human_RBP_ID_18188220,Human_RBP_ID_23154212,Human_RBP_ID_23510822,Human_RBP_ID_26803623,Human_RBP_ID_27203259,Human_RBP_ID_27412948 Human_Splice_Rec_1247650,Human_Splice_Rec_1247666,Human_Splice_Rec_1247706,Human_Splice_Rec_1247738 RMVar_hsa_circ_150163,RMVar_hsa_circ_84699,RMVar_hsa_circ_94236,RMVar_hsa_circ_105779,RMVar_hsa_circ_114841,RMVar_hsa_circ_122418,RMVar_hsa_circ_96626,RMVar_hsa_circ_87056,RMVar_hsa_circ_150167,RMVar_hsa_circ_150169,RMVar_hsa_circ_77955,RMVar_hsa_circ_150170,RMVar_hsa_circ_150168,RMVar_hsa_circ_150165,RMVar_hsa_circ_150166,RMVar_hsa_circ_150164 56426 RMVar_ID_56426 Human_SNP_ID_469224082 m1A Human chr11 - 62572612 62572612 62572612 CTTCCATTTTGGCCAAACCAACCGCACCCCTGAATTTCTCCGCAAATTTCCTGCCGGCAAGGTGA CTTCCATTTTGGCCAAACCAACCGCACCCCTGGATTTCTCCGCAAATTTCCTGCCGGCAAGGTGA T C AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:62571660..62572750 32194978 MeRIP-seq:(Medium) rs770416963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398848,Human_RBP_ID_870365,Human_RBP_ID_1265025,Human_RBP_ID_1354610,Human_RBP_ID_1458159,Human_RBP_ID_1780537,Human_RBP_ID_3377039,Human_RBP_ID_8353852,Human_RBP_ID_8770537,Human_RBP_ID_11656568,Human_RBP_ID_17232568,Human_RBP_ID_17348912,Human_RBP_ID_17465304,Human_RBP_ID_17649101,Human_RBP_ID_18188236,Human_RBP_ID_22491422,Human_RBP_ID_22891519,Human_RBP_ID_23510843,Human_RBP_ID_26892546,Human_RBP_ID_27618619 Human_Splice_Rec_1247635,Human_Splice_Rec_1247651,Human_Splice_Rec_1247667,Human_Splice_Rec_1247677,Human_Splice_Rec_1247691,Human_Splice_Rec_1247723 Human_miRNA_ID_2765517 RMVar_hsa_circ_31623,RMVar_hsa_circ_150163,RMVar_hsa_circ_96626,RMVar_hsa_circ_113242,RMVar_hsa_circ_150180,RMVar_hsa_circ_331488 56427 RMVar_ID_56427 Human_SNP_ID_469224091 m1A Human chr11 + 62572635 62572635 62572635 CGGAGAAATTCAGGGGTGCGGTTGGTTTGGCCAAAATGGAAGTGGGGTGGTGCGGAGAGCACGCG CGGAGAAATTCAGGGGTGCGGTTGGTTTGGCCGAAATGGAAGTGGGGTGGTGCGGAGAGCACGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:62572552..62572725;chr11:62572521..62572748;chr11:62572565..62572795;chr11:62572551..62572745;chr11:62572547..62572710 26863196 MeRIP-seq:(Medium) rs1260684608 Functional Loss SNV dbSNP153 33..33 33 - - - 56428 RMVar_ID_56428 Human_SNP_ID_469224251 m1A Human chr11 + 62573192 62573191 62573192 AGCATCGTCCTGTCTCTAAGGCACGCACGACGATCGAGAGATTTCTAGTTCCCCTCAGACTAGCC AGCATCGTCCTGTCTCTAAGGCACGCACGACG_TCGAGAGATTTCTAGTTCCCCTCAGACTAGCC GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62573188..62573486 32194978 MeRIP-seq:(Medium) rs1277448801 Functional Loss DEL dbSNP153 33..33 33 - - - 56429 RMVar_ID_56429 Human_SNP_ID_469224274 m1A Human chr11 - 62573281 62573280 62573282 CCGGAGGGATGATATTCGCGACACGGAAAGAAAGGCTTTTTGAGAGAGAGGAGTTGATTTAAGAA CCGGAGGGATGATATTCGCGACACGGAAAGA__GGCTTTTTGAGAGAGAGGAGTTGATTTAAGAA CTT C AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62573277..62573536 26863196 MeRIP-seq:(Medium) rs950737530 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11656593 RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56430 RMVar_ID_56430 Human_SNP_ID_469224275 m1A Human chr11 - 62573281 62573281 62573281 CCGGAGGGATGATATTCGCGACACGGAAAGAAAGGCTTTTTGAGAGAGAGGAGTTGATTTAAGAA CCGGAGGGATGATATTCGCGACACGGAAAGAAGGGCTTTTTGAGAGAGAGGAGTTGATTTAAGAA T C AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62573277..62573536 26863196 MeRIP-seq:(Medium) rs893248125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11656593 RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56431 RMVar_ID_56431 Human_SNP_ID_469224407 m1A Human chr11 - 62573764 62573764 62573764 TATCCACCGCCATCCTTTGCCCGAGTGGGGCCAGTCGGCGCCAGAGGAGTTCTGAGGTTGAGTGG TATCCACCGCCATCCTTTGCCCGAGTGGGGCCCGTCGGCGCCAGAGGAGTTCTGAGGTTGAGTGG T G AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr11:62573753..62573997;chr11:62573754..62573838 26863410 MeRIP-seq:(Medium) rs1313645400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5341389,Human_RBP_ID_11656622,Human_RBP_ID_19049526,Human_RBP_ID_23510851 RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56432 RMVar_ID_56432 Human_SNP_ID_469224827 m1A Human chr11 - 62574847 62574845 62574847 AGCACCGCGCGTGGCACCTGGCACCCGCGCAGAGTTCCTGAATGGCAGAGCGGTGGGTGGCTCCA AGCACCGCGCGTGGCACCTGGCACCCGCGCAG__TTCCTGAATGGCAGAGCGGTGGGTGGCTCCA ACT A AP002990.1 Ensembl:ENSG00000255508 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62574796..62574964 26863196 MeRIP-seq:(Medium) rs746717141 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_227382 Human_Splice_Rec_1247688,Human_Splice_Rec_1247722,Human_Splice_Rec_1247740 RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56433 RMVar_ID_56433 Human_SNP_ID_469224828 m1A Human chr11 - 62574847 62574847 62574847 AGCACCGCGCGTGGCACCTGGCACCCGCGCAGAGTTCCTGAATGGCAGAGCGGTGGGTGGCTCCA AGCACCGCGCGTGGCACCTGGCACCCGCGCAGGGTTCCTGAATGGCAGAGCGGTGGGTGGCTCCA T C AP002990.1 Ensembl:ENSG00000255508 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62574796..62574964 26863196 MeRIP-seq:(Medium) rs1351189748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227382 Human_Splice_Rec_1247688,Human_Splice_Rec_1247722,Human_Splice_Rec_1247740 RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56434 RMVar_ID_56434 Human_SNP_ID_469224855 m1A Human chr11 - 62574910 62574910 62574910 TGCTCTCCACCCCACCAGCTTCTCCTTCCTACAGTTCGCACAGCTCGAGGGGAGTGCGGGGGCAG TGCTCTCCACCCCACCAGCTTCTCCTTCCTACCGTTCGCACAGCTCGAGGGGAGTGCGGGGGCAG T G AP002990.1 Ensembl:ENSG00000255508 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62574869..62574941 26863196 MeRIP-seq:(Medium) rs1565264213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 56435 RMVar_ID_56435 Human_SNP_ID_469224953 m1A Human chr11 - 62575195 62575194 62575195 GCTTTGTGGCGTCTGTCTCCCCGGCTGACCGAATGCTCACTGTGACCCCGCTCCAGGATCCCCAA GCTTTGTGGCGTCTGTCTCCCCGGCTGACCGA_TGCTCACTGTGACCCCGCTCCAGGATCCCCAA AT A AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62575144..62575642 32194978 MeRIP-seq:(Medium) rs1565264422 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1458166,Human_RBP_ID_8246407,Human_RBP_ID_8353862 56436 RMVar_ID_56436 Human_SNP_ID_469224954 m1A Human chr11 - 62575195 62575195 62575195 GCTTTGTGGCGTCTGTCTCCCCGGCTGACCGAATGCTCACTGTGACCCCGCTCCAGGATCCCCAA GCTTTGTGGCGTCTGTCTCCCCGGCTGACCGAGTGCTCACTGTGACCCCGCTCCAGGATCCCCAA T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62575144..62575642 32194978 MeRIP-seq:(Medium) rs1216110823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1458166,Human_RBP_ID_8246407,Human_RBP_ID_8353862 56437 RMVar_ID_56437 Human_SNP_ID_469225152 m1A Human chr11 - 62575657 62575655 62575657 AGCAGGGATGTGCAGGGGACGGTGGGGAAGACAGGGTAGAAGAGATGGTTATAGAGGTTGGAGAG AGCAGGGATGTGCAGGGGACGGTGGGGAAGAC__GGTAGAAGAGATGGTTATAGAGGTTGGAGAG CCT C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:62575266..62575942;chr11:62575541..62575815 26863196 MeRIP-seq:(Medium) rs780651684 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_259722,Human_RBP_ID_8246411,Human_RBP_ID_18159691,Human_RBP_ID_18510668,Human_RBP_ID_18526351,Human_RBP_ID_18932443,Human_RBP_ID_21916926 56438 RMVar_ID_56438 Human_SNP_ID_469225605 m1A Human chr11 - 62576969 62576969 62576969 CAGTAACTACGCCCTGACCTTGCTGGTGATCTATTTTCTTCAGACCAGGGACCCTCCTGTGTTGC CAGTAACTACGCCCTGACCTTGCTGGTGATCTGTTTTCTTCAGACCAGGGACCCTCCTGTGTTGC T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62576855..62576976 26863196 MeRIP-seq:(Medium) rs756552162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_987652,Human_RBP_ID_1458169,Human_RBP_ID_22435362 Human_Splice_Rec_1247684,Human_Splice_Rec_1247685,Human_Splice_Rec_1247718,Human_Splice_Rec_1247719,Human_Splice_Rec_1247754,Human_Splice_Rec_1247755,Human_Splice_Rec_1247770,Human_Splice_Rec_1247771,Human_Splice_Rec_1247776,Human_Splice_Rec_1247778,Human_Splice_Rec_1247779 Human_miRNA_ID_2350179 RMVar_hsa_circ_55292,RMVar_hsa_circ_63139,RMVar_hsa_circ_365312,RMVar_hsa_circ_150183 56439 RMVar_ID_56439 Human_SNP_ID_469226245 m1A Human chr11 - 62578909 62578909 62578909 CCCTCCAGATTCACAACCTCCTGCTTCTCCCCAGGATTCTGAAGCCCTGGACTTTGAAACCCCTT CCCTCCAGATTCACAACCTCCTGCTTCTCCCCGGGATTCTGAAGCCCTGGACTTTGAAACCCCTT T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62578861..62579001 26863196 MeRIP-seq:(Medium) rs555954379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2040143,Human_miRNA_ID_2367239,Human_miRNA_ID_3015037,Human_miRNA_ID_3019125 RMVar_hsa_circ_23478,RMVar_hsa_circ_55292,RMVar_hsa_circ_63139,RMVar_hsa_circ_88200,RMVar_hsa_circ_150184 56440 RMVar_ID_56440 Human_SNP_ID_469226991 m1A Human chr11 - 62581541 62581541 62581541 GGCCTCCAAATCCCCCAAAGGAGCGGCCCCCGACAGTCACCAGCTGGCCAAAGCGCTAGCTGAGG GGCCTCCAAATCCCCCAAAGGAGCGGCCCCCGGCAGTCACCAGCTGGCCAAAGCGCTAGCTGAGG T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62581493..62589049 32194978 MeRIP-seq:(Medium) rs1329771650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4166565,Human_RBP_ID_17798118,Human_RBP_ID_18973794 Human_miRNA_ID_2037298,Human_miRNA_ID_2051736,Human_miRNA_ID_2348002 RMVar_hsa_circ_55292,RMVar_hsa_circ_63139,RMVar_hsa_circ_88200,RMVar_hsa_circ_150185,RMVar_hsa_circ_314420,RMVar_hsa_circ_150184,RMVar_hsa_circ_375054,RMVar_hsa_circ_150186,RMVar_hsa_circ_32168 56441 RMVar_ID_56441 Human_SNP_ID_469229527 m1A Human chr11 - 62591472 62591472 62591472 TCGGTACAGGAGAGTCGCTATGGCGGCGGTGGATTCGGATGTCGAATCGCTGCCGCGTGGGGGGT TCGGTACAGGAGAGTCGCTATGGCGGCGGTGGGTTCGGATGTCGAATCGCTGCCGCGTGGGGGGT T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62591421..62591505 26863196 MeRIP-seq:(Medium) rs778420150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184944,Human_RBP_ID_11656878,Human_RBP_ID_23124530,Human_RBP_ID_23207317 Human_Splice_Rec_1247707,Human_Splice_Rec_1247743,Human_Splice_Rec_1247759,Human_Splice_Rec_1247781,Human_Splice_Rec_1247791 56442 RMVar_ID_56442 Human_SNP_ID_469229543 m1A Human chr11 + 62591486 62591486 62591486 AGCGATTCGACATCCGAATCCACCGCCGCCATAGCGACTCTCCTGTACCGACAAAAACACAAGCA AGCGATTCGACATCCGAATCCACCGCCGCCATGGCGACTCTCCTGTACCGACAAAAACACAAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62591413..62591505 26863196 MeRIP-seq:(Medium) rs1464102751 Functional Loss SNV dbSNP153 33..33 33 - - - 56443 RMVar_ID_56443 Human_SNP_ID_469230089 m1A Human chr11 - 62593358 62593357 62593358 GAGTTTGAGGCCCCTAAGCTGGCATCAACCCCAGGCCACGCTCGCTCTTTCCTTCCCTCCCCTCC GAGTTTGAGGCCCCTAAGCTGGCATCAACCCC_GGCCACGCTCGCTCTTTCCTTCCCTCCCCTCC CT C MTA2 Ensembl:ENSG00000149480 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62593308..62593382 26863196 MeRIP-seq:(Medium) rs1485571631 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_226712,Human_RBP_ID_398860,Human_RBP_ID_4191904,Human_RBP_ID_5314204,Human_RBP_ID_6082391,Human_RBP_ID_8175771,Human_RBP_ID_8353878,Human_RBP_ID_11769719,Human_RBP_ID_18933562,Human_RBP_ID_24460411,Human_RBP_ID_26408574,Human_RBP_ID_26892574 Human_miRNA_ID_1988498 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56444 RMVar_ID_56444 Human_SNP_ID_469230147 m1A Human chr11 - 62593517 62593516 62593518 TGAAAGGGGATGGGGAGGGGAAGAGTAAACAGATAACAGGTGGTGGTACCTGGTTGGGGGAGGGG TGAAAGGGGATGGGGAGGGGAAGAGTAAACA__TAACAGGTGGTGGTACCTGGTTGGGGGAGGGG ATC A MTA2 Ensembl:ENSG00000149480 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62593467..62593581 26863196 MeRIP-seq:(Medium) rs80330686 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2273188,Human_RBP_ID_4191909,Human_RBP_ID_5138585,Human_RBP_ID_6082403,Human_RBP_ID_8175096,Human_RBP_ID_11759796,Human_RBP_ID_17648432,Human_RBP_ID_17798120,Human_RBP_ID_22896238,Human_RBP_ID_26408577 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56445 RMVar_ID_56445 Human_SNP_ID_469230148 m1A Human chr11 - 62593517 62593517 62593517 TGAAAGGGGATGGGGAGGGGAAGAGTAAACAGATAACAGGTGGTGGTACCTGGTTGGGGGAGGGG TGAAAGGGGATGGGGAGGGGAAGAGTAAACAGGTAACAGGTGGTGGTACCTGGTTGGGGGAGGGG T C MTA2 Ensembl:ENSG00000149480 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62593467..62593581 26863196 MeRIP-seq:(Medium) rs999883555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2273188,Human_RBP_ID_4191909,Human_RBP_ID_5138585,Human_RBP_ID_6082403,Human_RBP_ID_8175096,Human_RBP_ID_11759796,Human_RBP_ID_17648432,Human_RBP_ID_17798120,Human_RBP_ID_22896238,Human_RBP_ID_26408577 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56446 RMVar_ID_56446 Human_SNP_ID_469230149 m1A Human chr11 - 62593517 62593517 62593518 TGAAAGGGGATGGGGAGGGGAAGAGTAAACAGATAACAGGTGGTGGTACCTGGTTGGGGGAGGGG TGAAAGGGGATGGGGAGGGGAAGAGTAAACAAGTAACAGGTGGTGGTACCTGGTTGGGGGAGGGG TC CT MTA2 Ensembl:ENSG00000149480 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62593467..62593581 26863196 MeRIP-seq:(Medium) rs1554963431 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_2273188,Human_RBP_ID_4191909,Human_RBP_ID_5138585,Human_RBP_ID_6082403,Human_RBP_ID_8175096,Human_RBP_ID_11759796,Human_RBP_ID_17648432,Human_RBP_ID_17798120,Human_RBP_ID_22896238,Human_RBP_ID_26408577 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56447 RMVar_ID_56447 Human_SNP_ID_469230278 m1A Human chr11 + 62593926 62593926 62593926 GGCTCATTGGTGCTGGCAGGATGTGAGGGTGCAGGTAGAGGGACAGGGGGCCGCACTGCAATCAG GGCTCATTGGTGCTGGCAGGATGTGAGGGTGCTGGTAGAGGGACAGGGGGCCGCACTGCAATCAG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62593876..62593925 26863196 MeRIP-seq:(Medium) rs1415946197 Functional Loss SNV dbSNP153 33..33 33 - - - 56448 RMVar_ID_56448 Human_SNP_ID_469230322 m1A Human chr11 - 62594011 62594011 62594011 CAGGGCCCTACGGAAGGCTCTGACCCATCTGGAAATGCGGCGAGCTGCTCGCCGACCCAACTTGC CAGGGCCCTACGGAAGGCTCTGACCCATCTGGCAATGCGGCGAGCTGCTCGCCGACCCAACTTGC T G MTA2 Ensembl:ENSG00000149480 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62593926..62594050 32194978 MeRIP-seq:(Medium) rs1195259171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226146,Human_RBP_ID_398874,Human_RBP_ID_1458179,Human_RBP_ID_8773605,Human_RBP_ID_11656928,Human_RBP_ID_17350591,Human_RBP_ID_18609624,Human_RBP_ID_19049527,Human_RBP_ID_24912991 Human_Splice_Rec_1247830,Human_Splice_Rec_1247860,Human_Splice_Rec_1247894 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56449 RMVar_ID_56449 Human_SNP_ID_469230383 m1A Human chr11 - 62594255 62594255 62594255 GTGGTGTTTGTGGCCACAAAGGATACCAGGTAAGGCGTCTACCATGGGAGGGGCTGAGAGGGACA GTGGTGTTTGTGGCCACAAAGGATACCAGGTAGGGCGTCTACCATGGGAGGGGCTGAGAGGGACA T C MTA2 Ensembl:ENSG00000149480 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62594251..62594275 32194978 MeRIP-seq:(Medium) rs1485704060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19051788,Human_RBP_ID_22034515 RMVar_hsa_circ_75667,RMVar_hsa_circ_150188 56450 RMVar_ID_56450 Human_SNP_ID_469231565 m1A Human chr11 + 62598004 62598004 62598004 CCCCTTGGAATTAGACAACCTGGTAGCCGTACAGTCTTGTCCTGTTGCTTACCCTCTACTAGGCG CCCCTTGGAATTAGACAACCTGGTAGCCGTACCGTCTTGTCCTGTTGCTTACCCTCTACTAGGCG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62598001..62598075 32194978 MeRIP-seq:(Medium) rs759384107 Functional Loss SNV dbSNP153 33..33 33 - - - 56451 RMVar_ID_56451 Human_SNP_ID_469232676 m1A Human chr11 - 62601588 62601588 62601588 GCCGGGATGAACCGCGACGGCTGAGGCAGCGGAGGTGCCGGCTGCGCGGGCCCCAGTGAGACTCC GCCGGGATGAACCGCGACGGCTGAGGCAGCGGGGGTGCCGGCTGCGCGGGCCCCAGTGAGACTCC T C MTA2 Ensembl:ENSG00000149480 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:62601401..62601750 26863410 MeRIP-seq:(Medium) rs976973219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398889,Human_RBP_ID_4184124,Human_RBP_ID_5461127,Human_RBP_ID_8773619,Human_RBP_ID_9275775,Human_RBP_ID_18973804,Human_RBP_ID_22435365,Human_RBP_ID_22895549 56452 RMVar_ID_56452 Human_SNP_ID_469232707 m1A Human chr11 - 62601670 62601670 62601670 TCGTTCCGGAAGAAGCCGAGCGGACGGGGGCCAGCCTCAGCGTCCCGGGAGTGAGGCGATAGCTG TCGTTCCGGAAGAAGCCGAGCGGACGGGGGCCCGCCTCAGCGTCCCGGGAGTGAGGCGATAGCTG T G MTA2 Ensembl:ENSG00000149480 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62601426..62601800 26863196 MeRIP-seq:(Medium) rs1293400736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227744,Human_RBP_ID_4166693,Human_RBP_ID_8773620,Human_RBP_ID_9276468,Human_RBP_ID_18416562 56453 RMVar_ID_56453 Human_SNP_ID_469233057 m1A Human chr11 + 62602492 62602492 62602492 CCCGCCAGGCAGCGATCAAACGTCGAGGGAGGAGGCGGGGGACAGGGAGGGGGTTCGAGAGGGCG CCCGCCAGGCAGCGATCAAACGTCGAGGGAGGCGGCGGGGGACAGGGAGGGGGTTCGAGAGGGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62602444..62602554 26863196 MeRIP-seq:(Medium) rs1216902108 Functional Loss SNV dbSNP153 33..33 33 - - - 56454 RMVar_ID_56454 Human_SNP_ID_469233058 m1A Human chr11 + 62602492 62602492 62602492 CCCGCCAGGCAGCGATCAAACGTCGAGGGAGGAGGCGGGGGACAGGGAGGGGGTTCGAGAGGGCG CCCGCCAGGCAGCGATCAAACGTCGAGGGAGGTGGCGGGGGACAGGGAGGGGGTTCGAGAGGGCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62602444..62602554 26863196 MeRIP-seq:(Medium) rs1216902108 Functional Loss SNV dbSNP153 33..33 33 - - - 56455 RMVar_ID_56455 Human_SNP_ID_469233092 m1A Human chr11 + 62602550 62602550 62602550 GAGGGCGTGGCGGGCGCCGGCCCCGCGCCCCCAGCGCCCAGCACTCGCCACTGGAAGATGCTGGC GAGGGCGTGGCGGGCGCCGGCCCCGCGCCCCCCGCGCCCAGCACTCGCCACTGGAAGATGCTGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62602285..62602591 26863196 MeRIP-seq:(Medium) rs879143809 Functional Loss SNV dbSNP153 33..33 33 - - - 56456 RMVar_ID_56456 Human_SNP_ID_469233145 m1A Human chr11 - 62602672 62602672 62602672 CACCGCAACTCTTCCCTCCGGCCCAGGCGCCGAGCCGCATGTACGGGGGCCACGGCAGCCACGTG CACCGCAACTCTTCCCTCCGGCCCAGGCGCCGGGCCGCATGTACGGGGGCCACGGCAGCCACGTG T C EML3 Ensembl:ENSG00000149499 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62602267..62602967 32194978 MeRIP-seq:(Medium) rs773536629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9275777,Human_RBP_ID_18972072 Human_Splice_Rec_1247958,Human_Splice_Rec_1247998,Human_Splice_Rec_1248040,Human_Splice_Rec_1248054,Human_Splice_Rec_1248090,Human_Splice_Rec_1248130,Human_Splice_Rec_1248172,Human_Splice_Rec_1248212 RMVar_hsa_circ_98671,RMVar_hsa_circ_150199 56457 RMVar_ID_56457 Human_SNP_ID_469233278 m1A Human chr11 + 62602944 62602942 62602944 CCCGACCTCCTACCCACCGCCACCCACGGCCCAGAGCTACACCATTTCAGGCGCTCCGGCAGCCG CCCGACCTCCTACCCACCGCCACCCACGGCC__GAGCTACACCATTTCAGGCGCTCCGGCAGCCG CCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62602913..62603159 26863196 MeRIP-seq:(Medium) rs1321860452 Functional Loss DEL dbSNP153 32..33 33 - - - 56458 RMVar_ID_56458 Human_SNP_ID_469234039 m1A Human chr11 + 62605755 62605755 62605755 GCGGTTCTGGGAGGGGTGTGTGCAGAGCCCCCAGAGCTCATCAGTGTGGCCCTGCAGCACAGCAT GCGGTTCTGGGAGGGGTGTGTGCAGAGCCCCCGGAGCTCATCAGTGTGGCCCTGCAGCACAGCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62605704..62605841 26863196 MeRIP-seq:(Medium) rs1387813509 Functional Loss SNV dbSNP153 33..33 33 - - - 56459 RMVar_ID_56459 Human_SNP_ID_469236203 m1A Human chr11 + 62612492 62612492 62612492 GGCCCCCGGGTTGCTCCGAGCGGCGGCGGCGGAGGAGGCGTCTAAGCCGCGGGGGCCACGGCCGG GGCCCCCGGGTTGCTCCGAGCGGCGGCGGCGGCGGAGGCGTCTAAGCCGCGGGGGCCACGGCCGG A C ROM1 Ensembl:ENSG00000149489 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62612442..62612710 26863196 MeRIP-seq:(Medium) rs944860298 Functional Loss SNV dbSNP153 33..33 33 - - - 56460 RMVar_ID_56460 Human_SNP_ID_469236259 m1A Human chr11 - 62612627 62612627 62612627 GGGGGGTCTGGAGACTGCGGCCCCGGGCCCACAGCGCCCCCTCCAGGCCCCTTCCCCGCGCCCGA GGGGGGTCTGGAGACTGCGGCCCCGGGCCCACGGCGCCCCCTCCAGGCCCCTTCCCCGCGCCCGA T C EML3 Ensembl:ENSG00000149499 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:62612540..62612872 26863410 MeRIP-seq:(Medium) rs1341899225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184951 Human_Splice_Rec_1248259 56461 RMVar_ID_56461 Human_SNP_ID_469237887 m1A Human chr11 + 62617010 62617010 62617010 GGTGCTCACCTCCTCAAACAGCTCCCGGCTGTAGGTGTTGTCATCGTCAGCAAAGTAGACGACTC GGTGCTCACCTCCTCAAACAGCTCCCGGCTGTGGGTGTTGTCATCGTCAGCAAAGTAGACGACTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62617003..62617134 26863196 MeRIP-seq:(Medium) rs1565075995 Functional Loss SNV dbSNP153 33..33 33 - - - 56462 RMVar_ID_56462 Human_SNP_ID_469239074 m1A Human chr11 - 62620634 62620630 62620634 CCATGTGACTGCCTTCCTCCCCTGCGGGCAGCAGCCGAGCAGCTACGGCAGAAGGATCTGAGGAT CCATGTGACTGCCTTCCTCCCCTGCGGGCAGC____GAGCAGCTACGGCAGAAGGATCTGAGGAT CGGCT C B3GAT3 Ensembl:ENSG00000149541 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62620575..62621058 32194978 MeRIP-seq:(Medium) rs1307311023 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_398918,Human_RBP_ID_4184127 Human_Splice_Rec_1248280,Human_Splice_Rec_1248288,Human_Splice_Rec_1248298,Human_Splice_Rec_1248306,Human_Splice_Rec_1248318 56463 RMVar_ID_56463 Human_SNP_ID_469239501 m1A Human chr11 - 62621947 62621947 62621947 CCGCCTGCTCGGGCGCGGGCGGCGGCGCGGCCATGAAGCTGAAGCTGAAGAACGTGTTTCTCGCC CCGCCTGCTCGGGCGCGGGCGGCGGCGCGGCCTTGAAGCTGAAGCTGAAGAACGTGTTTCTCGCC T A B3GAT3 Ensembl:ENSG00000149541 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62621902..62622109 26863196 MeRIP-seq:(Medium) rs139759238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227761,Human_RBP_ID_4184129 Human_Splice_Rec_1248279,Human_Splice_Rec_1248287,Human_Splice_Rec_1248295,Human_Splice_Rec_1248305,Human_Splice_Rec_1248315 56464 RMVar_ID_56464 Human_SNP_ID_469239502 m1A Human chr11 - 62621947 62621947 62621947 CCGCCTGCTCGGGCGCGGGCGGCGGCGCGGCCATGAAGCTGAAGCTGAAGAACGTGTTTCTCGCC CCGCCTGCTCGGGCGCGGGCGGCGGCGCGGCCGTGAAGCTGAAGCTGAAGAACGTGTTTCTCGCC T C B3GAT3 Ensembl:ENSG00000149541 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62621902..62622109 26863196 MeRIP-seq:(Medium) rs139759238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227761,Human_RBP_ID_4184129 Human_Splice_Rec_1248279,Human_Splice_Rec_1248287,Human_Splice_Rec_1248295,Human_Splice_Rec_1248305,Human_Splice_Rec_1248315 56465 RMVar_ID_56465 Human_SNP_ID_469240612 m1A Human chr11 + 62625386 62625386 62625386 AGAAATGAAAGGTGGGAGAGCAATCTGGTGGGAGGGAAGGGGAAAAGGAGCCCTAACTCATTGCC AGAAATGAAAGGTGGGAGAGCAATCTGGTGGGCGGGAAGGGGAAAAGGAGCCCTAACTCATTGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62625338..62625464 26863196 MeRIP-seq:(Medium) rs1311934055 Functional Loss SNV dbSNP153 33..33 33 - - - 56466 RMVar_ID_56466 Human_SNP_ID_469240669 m1A Human chr11 + 62625572 62625572 62625572 GTGTTCGTAAGTGAATGTGCTCCAGTTAGAGCAACAGGATGTTGGGGGAATGAAGGGAAAGAGTT GTGTTCGTAAGTGAATGTGCTCCAGTTAGAGCCACAGGATGTTGGGGGAATGAAGGGAAAGAGTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62625241..62625663 26863196 MeRIP-seq:(Medium) rs980787363 Functional Loss SNV dbSNP153 33..33 33 - - - 56467 RMVar_ID_56467 Human_SNP_ID_469240975 m1A Human chr11 - 62626393 62626393 62626393 TTCTGGATGATGGGCACACGTTCAACTATCAGACTCGCCAAGAGTTCCTGCTGCGTCGATTCTCA TTCTGGATGATGGGCACACGTTCAACTATCAGTCTCGCCAAGAGTTCCTGCTGCGTCGATTCTCA T A GANAB Ensembl:ENSG00000089597 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs747146421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398964,Human_RBP_ID_1458194,Human_RBP_ID_1780576,Human_RBP_ID_8061923,Human_RBP_ID_8770578,Human_RBP_ID_17232584,Human_RBP_ID_18609660 Human_Splice_Rec_1248358,Human_Splice_Rec_1248359,Human_Splice_Rec_1248404,Human_Splice_Rec_1248405,Human_Splice_Rec_1248448,Human_Splice_Rec_1248449,Human_Splice_Rec_1248490,Human_Splice_Rec_1248491,Human_Splice_Rec_1248536,Human_Splice_Rec_1248537,Human_Splice_Rec_1248542,Human_Splice_Rec_1248543,Human_Splice_Rec_1248582,Human_Splice_Rec_1248583,Human_Splice_Rec_1248590 Human_miRNA_ID_40179,Human_miRNA_ID_68900,Human_miRNA_ID_596349,Human_miRNA_ID_2221925,Human_miRNA_ID_2484982,Human_miRNA_ID_3073359,Human_miRNA_ID_3088322 RMVar_hsa_circ_9328,RMVar_hsa_circ_87106,RMVar_hsa_circ_123661,RMVar_hsa_circ_150206,RMVar_hsa_circ_374039,RMVar_hsa_circ_150208,RMVar_hsa_circ_13747,RMVar_hsa_circ_150207 56468 RMVar_ID_56468 Human_SNP_ID_469241224 m1A Human chr11 - 62627030 62627030 62627030 CCTGGCCAAGGGGAGGTGAGTTAAGGAAGGGCATGGTGGGGAAAGATGGTGGAAGCCAAAGGAGG CCTGGCCAAGGGGAGGTGAGTTAAGGAAGGGCGTGGTGGGGAAAGATGGTGGAAGCCAAAGGAGG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62627026..62627125 32194978 MeRIP-seq:(Medium) rs1335285265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1248352,Human_Splice_Rec_1248398,Human_Splice_Rec_1248442,Human_Splice_Rec_1248484,Human_Splice_Rec_1248530,Human_Splice_Rec_1248576 RMVar_hsa_circ_2179,RMVar_hsa_circ_87106,RMVar_hsa_circ_91814,RMVar_hsa_circ_123661,RMVar_hsa_circ_150206,RMVar_hsa_circ_374039,RMVar_hsa_circ_150208,RMVar_hsa_circ_150207,RMVar_hsa_circ_109077,RMVar_hsa_circ_150210,RMVar_hsa_circ_81550,RMVar_hsa_circ_150209,RMVar_hsa_circ_95465,RMVar_hsa_circ_150211,RMVar_hsa_circ_150212 56469 RMVar_ID_56469 Human_SNP_ID_469243560 m1A Human chr11 + 62634737 62634737 62634737 CCAGCCCCCAGGCCCTACCTGGCTGTCCCACCACCGTCTCCTCCCCGTGCCAGACCTCACAACAC CCAGCCCCCAGGCCCTACCTGGCTGTCCCACCCCCGTCTCCTCCCCGTGCCAGACCTCACAACAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62634735..62634818 26863196 MeRIP-seq:(Medium) rs913925138 Functional Loss SNV dbSNP153 33..33 33 - - - 56470 RMVar_ID_56470 Human_SNP_ID_469243641 m1A Human chr11 - 62634965 62634965 62634965 TTCTGTCTCTGGTCGTGATGAGAACAGTGTGGAGTTAACCATGGCTGAGGGACCCTACAAGATCA TTCTGTCTCTGGTCGTGATGAGAACAGTGTGGCGTTAACCATGGCTGAGGGACCCTACAAGATCA T G GANAB Ensembl:ENSG00000089597 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62634741..62635017 26863196 MeRIP-seq:(Medium) rs995750907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29668,Human_RBP_ID_1780595,Human_RBP_ID_22032134,Human_RBP_ID_22753624,Human_RBP_ID_23113070,Human_RBP_ID_26892737 Human_Splice_Rec_1248326,Human_Splice_Rec_1248370,Human_Splice_Rec_1248416,Human_Splice_Rec_1248458,Human_Splice_Rec_1248504,Human_Splice_Rec_1248548,Human_Splice_Rec_1248598,Human_Splice_Rec_1248610,Human_Splice_Rec_1248618,Human_Splice_Rec_1248626,Human_Splice_Rec_1248632,Human_Splice_Rec_1248634,Human_Splice_Rec_1248640,Human_Splice_Rec_1248650 RMVar_hsa_circ_7705,RMVar_hsa_circ_91814,RMVar_hsa_circ_374039,RMVar_hsa_circ_150208,RMVar_hsa_circ_150209,RMVar_hsa_circ_113027,RMVar_hsa_circ_150215,RMVar_hsa_circ_307775,RMVar_hsa_circ_45571,RMVar_hsa_circ_150217,RMVar_hsa_circ_29326,RMVar_hsa_circ_150224,RMVar_hsa_circ_150222,RMVar_hsa_circ_102717,RMVar_hsa_circ_328332,RMVar_hsa_circ_297750,RMVar_hsa_circ_150225,RMVar_hsa_circ_101155,RMVar_hsa_circ_347735,RMVar_hsa_circ_320591 56471 RMVar_ID_56471 Human_SNP_ID_469244833 m1A Human chr11 - 62639033 62639033 62639033 CGGTTCAGGATTGATGAGCTGGAGCCTCGGCGACCCCGATACCGTGTACCAGATGTTTTGGTGGC CGGTTCAGGATTGATGAGCTGGAGCCTCGGCGGCCCCGATACCGTGTACCAGATGTTTTGGTGGC T C GANAB Ensembl:ENSG00000089597 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62638945..62639142 26863196 MeRIP-seq:(Medium) rs781152349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29669,Human_RBP_ID_398987,Human_RBP_ID_748734,Human_RBP_ID_1780596,Human_RBP_ID_4166941,Human_RBP_ID_5170225,Human_RBP_ID_9004622,Human_RBP_ID_11657464,Human_RBP_ID_17804615,Human_RBP_ID_18188242,Human_RBP_ID_18609690,Human_RBP_ID_18973834,Human_RBP_ID_22434517,Human_RBP_ID_22753630,Human_RBP_ID_23510981,Human_RBP_ID_27203406 Human_Splice_Rec_1248324,Human_Splice_Rec_1248325,Human_Splice_Rec_1248368,Human_Splice_Rec_1248369,Human_Splice_Rec_1248414,Human_Splice_Rec_1248415,Human_Splice_Rec_1248456,Human_Splice_Rec_1248457,Human_Splice_Rec_1248502,Human_Splice_Rec_1248503,Human_Splice_Rec_1248596,Human_Splice_Rec_1248597,Human_Splice_Rec_1248608,Human_Splice_Rec_1248609,Human_Splice_Rec_1248624,Human_Splice_Rec_1248625,Human_Splice_Rec_1248630,Human_Splice_Rec_1248631,Human_Splice_Rec_1248638,Human_Splice_Rec_1248639,Human_Splice_Rec_1248648,Human_Splice_Rec_1248649 Human_miRNA_ID_238215 RMVar_hsa_circ_7705,RMVar_hsa_circ_91814,RMVar_hsa_circ_374039,RMVar_hsa_circ_150208,RMVar_hsa_circ_150209,RMVar_hsa_circ_307775,RMVar_hsa_circ_150217,RMVar_hsa_circ_29326,RMVar_hsa_circ_150224,RMVar_hsa_circ_150222,RMVar_hsa_circ_102717,RMVar_hsa_circ_297750,RMVar_hsa_circ_347735,RMVar_hsa_circ_320591,RMVar_hsa_circ_150227,RMVar_hsa_circ_90843,RMVar_hsa_circ_279294,RMVar_hsa_circ_150226 56472 RMVar_ID_56472 Human_SNP_ID_469245087 m1A Human chr11 + 62639719 62639719 62639719 CCCAGGCAGACCCCTAAAAAAGCCAGTACCAAAGACGCCCAAGACCTAAGGAGAAAAGGACAAAG CCCAGGCAGACCCCTAAAAAAGCCAGTACCAACGACGCCCAAGACCTAAGGAGAAAAGGACAAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:62639603..62639932;chr11:62639591..62639932 26863196 MeRIP-seq:(Medium) rs775672548 Functional Loss SNV dbSNP153 33..33 33 - - - 56473 RMVar_ID_56473 Human_SNP_ID_469245091 m1A Human chr11 + 62639728 62639728 62639728 ACCCCTAAAAAAGCCAGTACCAAAGACGCCCAAGACCTAAGGAGAAAAGGACAAAGACAGAGCAA ACCCCTAAAAAAGCCAGTACCAAAGACGCCCAGGACCTAAGGAGAAAAGGACAAAGACAGAGCAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:62639626..62639932;chr11:62639596..62639932 26863196 MeRIP-seq:(Medium) rs1373220171 Functional Loss SNV dbSNP153 33..33 33 - - - 56474 RMVar_ID_56474 Human_SNP_ID_469245092 m1A Human chr11 + 62639730 62639730 62639730 CCCTAAAAAAGCCAGTACCAAAGACGCCCAAGACCTAAGGAGAAAAGGACAAAGACAGAGCAATC CCCTAAAAAAGCCAGTACCAAAGACGCCCAAGGCCTAAGGAGAAAAGGACAAAGACAGAGCAATC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr11:62639651..62639775;chr11:62639651..62639774 26863410 MeRIP-seq:(Medium) rs762092056 Functional Loss SNV dbSNP153 33..33 33 - - - 56475 RMVar_ID_56475 Human_SNP_ID_469247263 m1A Human chr11 + 62646517 62646516 62646517 CACACAGGAAGGAGTGGAATGGGACTTGGGGGATCTGGGGGCGTCCCGGGCGCGCCCCCAGATTC CACACAGGAAGGAGTGGAATGGGACTTGGGGG_TCTGGGGGCGTCCCGGGCGCGCCCCCAGATTC GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62646511..62646650 26863196 MeRIP-seq:(Medium) rs990540671 Functional Loss DEL dbSNP153 33..33 33 - - - 56476 RMVar_ID_56476 Human_SNP_ID_469252868 m1A Human chr11 - 62664855 62664855 62664855 CCAAGGGCTGATCACGCGGCACCACCTCAAGAAGCGGGCGTAAGTACTAGACCCTCTTCCTGTTG CCAAGGGCTGATCACGCGGCACCACCTCAAGAGGCGGGCGTAAGTACTAGACCCTCTTCCTGTTG T C C11orf98,LBHD1,AP001458.2 Ensembl:ENSG00000278615,Ensembl:ENSG00000162194,Ensembl:ENSG00000255432 Protein coding,Protein coding,Protein coding exon,CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62649981..62667242 32194978 MeRIP-seq:(Medium) rs1450071007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362357,Human_RBP_ID_26317792 Human_Splice_Rec_1248655,Human_Splice_Rec_1248659,Human_Splice_Rec_1248665,Human_Splice_Rec_1248671,Human_Splice_Rec_1248681,Human_Splice_Rec_1248689,Human_Splice_Rec_1248701 Human_miRNA_ID_2865603 RMVar_hsa_circ_108643,RMVar_hsa_circ_150232,RMVar_hsa_circ_37168,RMVar_hsa_circ_324592 56477 RMVar_ID_56477 Human_SNP_ID_469255705 m1A Human chr11 - 62672124 62672124 62672124 CGCCCAAGCCAAGGTCCGGCGCCCACGGAGGCAAGTCCGGTCTCACGGTGACCTCCCGCCGGCGC CGCCCAAGCCAAGGTCCGGCGCCCACGGAGGCGAGTCCGGTCTCACGGTGACCTCCCGCCGGCGC T C LBHD1 Ensembl:ENSG00000162194 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62671988..62672225 32194978 MeRIP-seq:(Medium) rs1225146280 Functional Loss SNV dbSNP153 33..33 33 - - - 56478 RMVar_ID_56478 Human_SNP_ID_469257073 m1A Human chr11 - 62676590 62676590 62676590 GTTCTCATTGTGGCCAAGAAATGTCCCAGCTGAGGGCCTTTGTCCCATTGTCCCTCTGTGACCCC GTTCTCATTGTGGCCAAGAAATGTCCCAGCTGCGGGCCTTTGTCCCATTGTCCCTCTGTGACCCC T G UBXN1 Ensembl:ENSG00000162191 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62676526..62676782 32194978 MeRIP-seq:(Medium) rs1384834474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399037,Human_RBP_ID_749998,Human_RBP_ID_1780610,Human_RBP_ID_3939242,Human_RBP_ID_8354007,Human_RBP_ID_11658186,Human_RBP_ID_17648436,Human_RBP_ID_26768130 Human_Splice_Rec_1248788,Human_Splice_Rec_1248794,Human_Splice_Rec_1248806,Human_Splice_Rec_1248816,Human_Splice_Rec_1248832,Human_Splice_Rec_1248846,Human_Splice_Rec_1248864 RMVar_hsa_circ_79338,RMVar_hsa_circ_86665,RMVar_hsa_circ_88675,RMVar_hsa_circ_89794,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150235,RMVar_hsa_circ_150236,RMVar_hsa_circ_150237,RMVar_hsa_circ_150234 56479 RMVar_ID_56479 Human_SNP_ID_469257585 m1A Human chr11 - 62678036 62678036 62678036 AACGGGAGGCATTGGAACGGGAACGGCAGCGCAGGAGACAAGGGCAAGAGTTGTCAGCAGCACGA AACGGGAGGCATTGGAACGGGAACGGCAGCGCCGGAGACAAGGGCAAGAGTTGTCAGCAGCACGA T G UBXN1 Ensembl:ENSG00000162191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62677514..62678138 26863196 MeRIP-seq:(Medium) rs758629544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226798,Human_RBP_ID_399045,Human_RBP_ID_808908,Human_RBP_ID_5110786,Human_RBP_ID_5549507,Human_RBP_ID_22532357,Human_RBP_ID_26318526 Human_Splice_Rec_1248758,Human_Splice_Rec_1248770,Human_Splice_Rec_1248780,Human_Splice_Rec_1248798,Human_Splice_Rec_1248812,Human_Splice_Rec_1248824,Human_Splice_Rec_1248825,Human_Splice_Rec_1248840,Human_Splice_Rec_1248856,Human_Splice_Rec_1248868,Human_Splice_Rec_1248880,Human_Splice_Rec_1248892,Human_Splice_Rec_1248904,Human_Splice_Rec_1248916,Human_Splice_Rec_1248928 RMVar_hsa_circ_86665,RMVar_hsa_circ_88675,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150235,RMVar_hsa_circ_150234,RMVar_hsa_circ_62598 56480 RMVar_ID_56480 Human_SNP_ID_469257597 m1A Human chr11 + 62678057 62678057 62678057 CCCTTGTCTCCTGCGCTGCCGTTCCCGTTCCAATGCCTCCCGTTCCTCTCTTTCTTCACGCTCCC CCCTTGTCTCCTGCGCTGCCGTTCCCGTTCCAGTGCCTCCCGTTCCTCTCTTTCTTCACGCTCCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62677891..62678093 26863196 MeRIP-seq:(Medium) rs371951393 Functional Loss SNV dbSNP153 33..33 33 - - - 56481 RMVar_ID_56481 Human_SNP_ID_469257734 m1A Human chr11 - 62678328 62678328 62678328 AAAGACAGGAACAAACTAAGAGGTACAGTAACAACAATCTCACGTGTCTGAGGGTCGTCTTCCAT AAAGACAGGAACAAACTAAGAGGTACAGTAACGACAATCTCACGTGTCTGAGGGTCGTCTTCCAT T C UBXN1 Ensembl:ENSG00000162191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:62678326..62678425 26863196 MeRIP-seq:(Medium) rs1554981219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5345332 Human_Splice_Rec_1248756,Human_Splice_Rec_1248768,Human_Splice_Rec_1248778,Human_Splice_Rec_1248810,Human_Splice_Rec_1248822,Human_Splice_Rec_1248838,Human_Splice_Rec_1248854,Human_Splice_Rec_1248866,Human_Splice_Rec_1248878,Human_Splice_Rec_1248890,Human_Splice_Rec_1248902,Human_Splice_Rec_1248914,Human_Splice_Rec_1248922,Human_Splice_Rec_1248934 RMVar_hsa_circ_86665,RMVar_hsa_circ_88675,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150235,RMVar_hsa_circ_150234,RMVar_hsa_circ_62598 56482 RMVar_ID_56482 Human_SNP_ID_469257867 m1A Human chr11 - 62678597 62678597 62678597 TAACCTCCCCGCCCACTTTCCCTGCCAGGCTGATGGAGCACGAAGACGACCCCGATGTGGACGAG TAACCTCCCCGCCCACTTTCCCTGCCAGGCTGGTGGAGCACGAAGACGACCCCGATGTGGACGAG T C UBXN1 Ensembl:ENSG00000162191 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62678476..62678600 26863196 MeRIP-seq:(Medium) rs1345593745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4167123,Human_RBP_ID_5341418 Human_Splice_Rec_1248754,Human_Splice_Rec_1248766,Human_Splice_Rec_1248776,Human_Splice_Rec_1248808,Human_Splice_Rec_1248820,Human_Splice_Rec_1248836,Human_Splice_Rec_1248852,Human_Splice_Rec_1248876,Human_Splice_Rec_1248888,Human_Splice_Rec_1248900,Human_Splice_Rec_1248912,Human_Splice_Rec_1248920,Human_Splice_Rec_1248926,Human_Splice_Rec_1248932,Human_Splice_Rec_1248936 RMVar_hsa_circ_86665,RMVar_hsa_circ_88675,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150235,RMVar_hsa_circ_150234,RMVar_hsa_circ_62598 56483 RMVar_ID_56483 Human_SNP_ID_469258101 m1A Human chr11 - 62679006 62679006 62679006 GTGAGAGAGCGAGCGCCCGTCGGCGGGTGTCGAGGGCGGGTTGCCTCGCGCTGACCCTTCCCGCC GTGAGAGAGCGAGCGCCCGTCGGCGGGTGTCGCGGGCGGGTTGCCTCGCGCTGACCCTTCCCGCC T G UBXN1 Ensembl:ENSG00000162191 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:62678851..62679050 26863410 MeRIP-seq:(Medium) rs1301613879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184970,Human_RBP_ID_5110788,Human_RBP_ID_9321466,Human_RBP_ID_18416567,Human_RBP_ID_23511037 RMVar_hsa_circ_88675,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150234 56484 RMVar_ID_56484 Human_SNP_ID_469258105 m1A Human chr11 + 62679011 62679011 62679011 GAAGGGTCAGCGCGAGGCAACCCGCCCTCGACACCCGCCGACGGGCGCTCGCTCTCTCACCCGGC GAAGGGTCAGCGCGAGGCAACCCGCCCTCGACCCCCGCCGACGGGCGCTCGCTCTCTCACCCGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62678844..62679075 26863196 MeRIP-seq:(Medium) rs930726326 Functional Loss SNV dbSNP153 33..33 33 - - - 56485 RMVar_ID_56485 Human_SNP_ID_469261636 m1A Human chr11 - 62690479 62690479 62690479 CTGGGAAGATGCAGCTTTGCTGACGGAGGCCAACCTGCCTGCTCCTGCTCCTGCTTCTGCTTCTG CTGGGAAGATGCAGCTTTGCTGACGGAGGCCATCCTGCCTGCTCCTGCTCCTGCTTCTGCTTCTG T A HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding 3'UTR,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1450251165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399062,Human_RBP_ID_865079,Human_RBP_ID_17232590,Human_RBP_ID_18159221,Human_RBP_ID_18973845 Human_Splice_Rec_1248946,Human_Splice_Rec_1248968,Human_Splice_Rec_1248974,Human_Splice_Rec_1248992,Human_Splice_Rec_1249012,Human_Splice_Rec_1249016,Human_Splice_Rec_1249040,Human_Splice_Rec_1249060,Human_Splice_Rec_1249080,Human_Splice_Rec_1249100,Human_Splice_Rec_1249234 Human_miRNA_ID_722396,Human_miRNA_ID_722397 56486 RMVar_ID_56486 Human_SNP_ID_469265284 m1A Human chr11 - 62702417 62702417 62702417 GAGAGGTTTCATTAGAGCTTTGATGACTCAAAATAGGAAGACTTGAGAAAGGCCTAGAGAGAAGG GAGAGGTTTCATTAGAGCTTTGATGACTCAAAGTAGGAAGACTTGAGAAAGGCCTAGAGAGAAGG T C HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62702412..62702483 26863196 MeRIP-seq:(Medium) rs1204749563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11658382 RMVar_hsa_circ_37267,RMVar_hsa_circ_93870,RMVar_hsa_circ_150239,RMVar_hsa_circ_113516,RMVar_hsa_circ_104086,RMVar_hsa_circ_125292,RMVar_hsa_circ_150243,RMVar_hsa_circ_150244,RMVar_hsa_circ_371598,RMVar_hsa_circ_271762,RMVar_hsa_circ_83772,RMVar_hsa_circ_103708,RMVar_hsa_circ_81551,RMVar_hsa_circ_150246,RMVar_hsa_circ_150248,RMVar_hsa_circ_150249,RMVar_hsa_circ_150250,RMVar_hsa_circ_150247,RMVar_hsa_circ_150245 56487 RMVar_ID_56487 Human_SNP_ID_469266168 m1A Human chr11 + 62705318 62705318 62705318 GAAGGCCCCTCTCACCTGTAGTAGAAATGCACAGGGCTGAGGTGGCTGACTGTCGGCATATAGGA GAAGGCCCCTCTCACCTGTAGTAGAAATGCACGGGGCTGAGGTGGCTGACTGTCGGCATATAGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62705301..62705350 26863196 MeRIP-seq:(Medium) rs773926348 Functional Loss SNV dbSNP153 33..33 33 - - - 56488 RMVar_ID_56488 Human_SNP_ID_469266244 m1A Human chr11 - 62705533 62705533 62705533 CAGCTAGGAACGCAAGGCCTGAACCTGGGGCCAGACACCCTGCTCTCCCGGCCATGGTCAACGAC CAGCTAGGAACGCAAGGCCTGAACCTGGGGCCGGACACCCTGCTCTCCCGGCCATGGTCAACGAC T C HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:62705374..62706270;chr11:62705321..62705966 26863196 MeRIP-seq:(Medium) rs1284357129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184972 Human_Splice_Rec_1248950,Human_Splice_Rec_1248976,Human_Splice_Rec_1248994,Human_Splice_Rec_1249022,Human_Splice_Rec_1249042,Human_Splice_Rec_1249062,Human_Splice_Rec_1249082,Human_Splice_Rec_1249140,Human_Splice_Rec_1249148,Human_Splice_Rec_1249149,Human_Splice_Rec_1249154,Human_Splice_Rec_1249155,Human_Splice_Rec_1249164,Human_Splice_Rec_1249172,Human_Splice_Rec_1249178,Human_Splice_Rec_1249182,Human_Splice_Rec_1249216 RMVar_hsa_circ_37267,RMVar_hsa_circ_113516,RMVar_hsa_circ_104086,RMVar_hsa_circ_125292,RMVar_hsa_circ_150243,RMVar_hsa_circ_150244,RMVar_hsa_circ_371598,RMVar_hsa_circ_83772,RMVar_hsa_circ_103708,RMVar_hsa_circ_81551,RMVar_hsa_circ_150246,RMVar_hsa_circ_150248,RMVar_hsa_circ_150249,RMVar_hsa_circ_150250,RMVar_hsa_circ_150247,RMVar_hsa_circ_53080 56489 RMVar_ID_56489 Human_SNP_ID_469269131 m1A Human chr11 + 62714840 62714840 62714840 CTCTCCCTCTGTCCCCACTCCTGCCTGCTCCTACCTGCTGTGGAGAGCACCCTCGCGCTGCCTCC CTCTCCCTCTGTCCCCACTCCTGCCTGCTCCTGCCTGCTGTGGAGAGCACCCTCGCGCTGCCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:62714751..62714975;chr11:62714726..62715150 26863196 MeRIP-seq:(Medium) rs957867244 Functional Loss SNV dbSNP153 33..33 33 - - - 56490 RMVar_ID_56490 Human_SNP_ID_469269144 m1A Human chr11 - 62714879 62714879 62714879 CAAGTAAAGGAGAGTGATGAGGTGGTGTGGGGAGGGTGGGGAGGCAGCGCGAGGGTGCTCTCCAC CAAGTAAAGGAGAGTGATGAGGTGGTGTGGGGTGGGTGGGGAGGCAGCGCGAGGGTGCTCTCCAC T A HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62714799..62714922 26863196 MeRIP-seq:(Medium) rs1198466760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32007,Human_RBP_ID_809246,Human_RBP_ID_6082732,Human_RBP_ID_18932460,Human_RBP_ID_26320012 Human_miRNA_ID_656809 RMVar_hsa_circ_113516,RMVar_hsa_circ_104086,RMVar_hsa_circ_150243,RMVar_hsa_circ_150244,RMVar_hsa_circ_103708,RMVar_hsa_circ_81551,RMVar_hsa_circ_150249,RMVar_hsa_circ_150250,RMVar_hsa_circ_63600,RMVar_hsa_circ_53080 56491 RMVar_ID_56491 Human_SNP_ID_469269418 m1A Human chr11 - 62715529 62715529 62715529 TTTACGGGCGAGATTATGAGTACAACAGATACAGAGACTATTACAGACAATACAATCGGGATGTG TTTACGGGCGAGATTATGAGTACAACAGATACGGAGACTATTACAGACAATACAATCGGGATGTG T C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62715176..62715622 26863196 MeRIP-seq:(Medium) rs1023724705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780628,Human_RBP_ID_5554393,Human_RBP_ID_9254679,Human_RBP_ID_9362363,Human_RBP_ID_11658828,Human_RBP_ID_22435392,Human_RBP_ID_22891629 Human_Splice_Rec_1249212,Human_Splice_Rec_1249213,Human_Splice_Rec_1249262,Human_Splice_Rec_1249263 RMVar_hsa_circ_113516,RMVar_hsa_circ_104086,RMVar_hsa_circ_150243,RMVar_hsa_circ_150244,RMVar_hsa_circ_103708,RMVar_hsa_circ_81551,RMVar_hsa_circ_150249,RMVar_hsa_circ_150250,RMVar_hsa_circ_63600,RMVar_hsa_circ_53080,RMVar_hsa_circ_354740,RMVar_hsa_circ_365005,RMVar_hsa_circ_346774 56492 RMVar_ID_56492 Human_SNP_ID_469271975 m1A Human chr11 - 62723628 62723628 62723628 AGTTCCCCACCCTTTGGTCTGGGGCAAGGAGTACTTACGGAGTGACAAAGGGAAAAGTCTGCTTT AGTTCCCCACCCTTTGGTCTGGGGCAAGGAGTGCTTACGGAGTGACAAAGGGAAAAGTCTGCTTT T C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:62723626..62723650 26863196 MeRIP-seq:(Medium) rs758282858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064959,Human_RBP_ID_5460517,Human_RBP_ID_5520767,Human_RBP_ID_8773639,Human_RBP_ID_9254689,Human_RBP_ID_9275826,Human_RBP_ID_9362376,Human_RBP_ID_18973854,Human_RBP_ID_23511154,Human_RBP_ID_26317794,Human_RBP_ID_26892959 Human_Splice_Rec_1249194,Human_Splice_Rec_1249195,Human_Splice_Rec_1249244,Human_Splice_Rec_1249245,Human_Splice_Rec_1249265 RMVar_hsa_circ_11153,RMVar_hsa_circ_104086,RMVar_hsa_circ_150244,RMVar_hsa_circ_63600,RMVar_hsa_circ_53080,RMVar_hsa_circ_354740,RMVar_hsa_circ_365005,RMVar_hsa_circ_346774,RMVar_hsa_circ_280748,RMVar_hsa_circ_314710,RMVar_hsa_circ_72083,RMVar_hsa_circ_150253,RMVar_hsa_circ_302344,RMVar_hsa_circ_65521,RMVar_hsa_circ_66238,RMVar_hsa_circ_150254,RMVar_hsa_circ_150255,RMVar_hsa_circ_12836,RMVar_hsa_circ_70138,RMVar_hsa_circ_270201 56493 RMVar_ID_56493 Human_SNP_ID_469272093 m1A Human chr11 - 62723985 62723984 62723986 TGTTTCTTTTCTATCTTACATATATAGCTCAAAGTCTCCACTGCCTCCTGAAGAAGAGGCAAAAG TGTTTCTTTTCTATCTTACATATATAGCTCA__GTCTCCACTGCCTCCTGAAGAAGAGGCAAAAG CTT C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62723901..62724000 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 32..33 33 - - - Human_RBP_ID_32025,Human_RBP_ID_869582,Human_RBP_ID_2273342,Human_RBP_ID_9275828,Human_RBP_ID_9362377,Human_RBP_ID_22895352,Human_RBP_ID_24892888,Human_RBP_ID_26318544,Human_RBP_ID_27413180 Human_Splice_Rec_1249192,Human_Splice_Rec_1249193,Human_Splice_Rec_1249242,Human_Splice_Rec_1249243 RMVar_hsa_circ_11153,RMVar_hsa_circ_104086,RMVar_hsa_circ_150244,RMVar_hsa_circ_63600,RMVar_hsa_circ_53080,RMVar_hsa_circ_354740,RMVar_hsa_circ_365005,RMVar_hsa_circ_280748,RMVar_hsa_circ_72083,RMVar_hsa_circ_150253,RMVar_hsa_circ_302344,RMVar_hsa_circ_65521,RMVar_hsa_circ_150254,RMVar_hsa_circ_150255,RMVar_hsa_circ_70138,RMVar_hsa_circ_270201,RMVar_hsa_circ_339026 56494 RMVar_ID_56494 Human_SNP_ID_469272231 m1A Human chr11 - 62724401 62724401 62724401 TTTGTAGGAGATGACCAGGATAGTGAAAAGTCAAAACCAGCAGGCTCAGATGGTGAGCGGCGGGG TTTGTAGGAGATGACCAGGATAGTGAAAAGTCCAAACCAGCAGGCTCAGATGGTGAGCGGCGGGG T G HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62724351..62724425 26863196 MeRIP-seq:(Medium) rs765433132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4192181,Human_RBP_ID_11658978,Human_RBP_ID_22891644 Human_Splice_Rec_1249190,Human_Splice_Rec_1249240 RMVar_hsa_circ_11153,RMVar_hsa_circ_104086,RMVar_hsa_circ_150244,RMVar_hsa_circ_63600,RMVar_hsa_circ_354740,RMVar_hsa_circ_280748,RMVar_hsa_circ_150253,RMVar_hsa_circ_302344,RMVar_hsa_circ_150254,RMVar_hsa_circ_150255,RMVar_hsa_circ_270201,RMVar_hsa_circ_339026 56495 RMVar_ID_56495 Human_SNP_ID_469272968 m1A Human chr11 - 62726681 62726681 62726681 CCTCGGCAAGAGGGAGGAAGACGAACCCGAGGAGCGGAGCGGGGACGAGACGCCGGGATCCGAGG CCTCGGCAAGAGGGAGGAAGACGAACCCGAGGGGCGGAGCGGGGACGAGACGCCGGGATCCGAGG T C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62724392..62726742 26863196 MeRIP-seq:(Medium) rs1390436078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32721,Human_RBP_ID_228127,Human_RBP_ID_867582,Human_RBP_ID_5138604,Human_RBP_ID_9275830,Human_RBP_ID_9362379,Human_RBP_ID_17648770,Human_RBP_ID_18973855,Human_RBP_ID_26318546 Human_Splice_Rec_1249189,Human_Splice_Rec_1249239 56496 RMVar_ID_56496 Human_SNP_ID_469273171 m1A Human chr11 + 62726974 62726974 62726974 CCCGGGCCGCCGCCCGACGCGGCCACAGGCCGAGGCTCCGCCTTGCAGGCCCCGCCGGGCCCGGC CCCGGGCCGCCGCCCGACGCGGCCACAGGCCGGGGCTCCGCCTTGCAGGCCCCGCCGGGCCCGGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr11:62726926..62727100;chr11:62726925..62727244 26863196,26863410 MeRIP-seq:(Medium) rs1421611784 Functional Loss SNV dbSNP153 33..33 33 - - - 56497 RMVar_ID_56497 Human_SNP_ID_469273200 m1A Human chr11 - 62727023 62727008 62727023 GGAGGCGCTGGACGCCGAGATGCTCGAGGACGAGGCCGGCGGCGGCGGGGCCGGGCCCGGCGGGG GGAGGCGCTGGACGCCGAGATGCTCGAGGACG_______________GGGCCGGGCCCGGCGGGG CCGCCGCCGCCGGCCT C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:62726923..62727099 26863410 MeRIP-seq:(Medium) rs769304660 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_32723,Human_RBP_ID_8773642,Human_RBP_ID_9275836,Human_RBP_ID_22895355 56498 RMVar_ID_56498 Human_SNP_ID_469273264 m1A Human chr11 - 62727152 62727152 62727152 GCGGGAGGCGGAGGAGGCGGCGGCGGCGATGGAGGTGAAGCGGCTGAAAGTGACCGAGCTGCGGT GCGGGAGGCGGAGGAGGCGGCGGCGGCGATGGGGGTGAAGCGGCTGAAAGTGACCGAGCTGCGGT T C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr11:62723894..62727500;chr11:62726600..62727558;chr11:62722626..62727500;chr11:62723901..62727525;chr11:62724301..62727375 26863196 MeRIP-seq:(Medium) rs1412179550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31259,Human_RBP_ID_751797,Human_RBP_ID_3940624,Human_RBP_ID_4167383,Human_RBP_ID_5138605,Human_RBP_ID_5520768,Human_RBP_ID_8774310,Human_RBP_ID_9275838,Human_RBP_ID_9321468,Human_RBP_ID_9362381,Human_RBP_ID_17067002,Human_RBP_ID_18972099,Human_RBP_ID_22035916,Human_RBP_ID_22433680,Human_RBP_ID_22532358,Human_RBP_ID_22709166,Human_RBP_ID_22895048,Human_RBP_ID_26318548,Human_RBP_ID_27803511,Human_RBP_ID_27836336 56499 RMVar_ID_56499 Human_SNP_ID_469274026 m1A Human chr11 + 62728550 62728550 62728550 TCCTGAGTAGGGCCTTGCTTGAGTTCTTCGGAAAGTCTCATCCACCCCCACATCGCCTCTTTAGG TCCTGAGTAGGGCCTTGCTTGAGTTCTTCGGACAGTCTCATCCACCCCCACATCGCCTCTTTAGG A C TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62728519..62728609 26863196 MeRIP-seq:(Medium) rs751913787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1458261,Human_RBP_ID_17649624 56500 RMVar_ID_56500 Human_SNP_ID_469277559 m1A Human chr11 + 62739830 62739830 62739830 TATTTCCTTTTTAGTAGAGACATGGTTTTGCCATGTTGGCCAGGGTGCTCTTGAACTCCTGGCCT TATTTCCTTTTTAGTAGAGACATGGTTTTGCCTTGTTGGCCAGGGTGCTCTTGAACTCCTGGCCT A T TTC9C Ensembl:ENSG00000162222 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1257855879 Functional Loss SNV dbSNP153 33..33 33 - - - 56501 RMVar_ID_56501 Human_SNP_ID_469282018 m1A Human chr11 + 62754011 62754011 62754011 GGCTCCACGAAGTAGAGATCTTTTTCGCTCCCAGGCCTTGCCAGGCGATGCCTCTACGCCCCACT GGCTCCACGAAGTAGAGATCTTTTTCGCTCCCGGGCCTTGCCAGGCGATGCCTCTACGCCCCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62754005..62754123 26863196 MeRIP-seq:(Medium) rs760402045 Functional Loss SNV dbSNP153 33..33 33 - - - 56502 RMVar_ID_56502 Human_SNP_ID_469284516 m1A Human chr11 - 62761625 62761625 62761625 GTAGAACATCTTCCCAGACCAGGTAGGCAGGCAGAGTCCACACCTCCGACAGTCCCTGGGAATCC GTAGAACATCTTCCCAGACCAGGTAGGCAGGCGGAGTCCACACCTCCGACAGTCCCTGGGAATCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:62761576..62761698;chr11:62761576..62761957;chr11:62761576..62761840 26863196 MeRIP-seq:(Medium) rs1028717004 Functional Loss SNV dbSNP153 33..33 33 - - - 56503 RMVar_ID_56503 Human_SNP_ID_469284619 m1A Human chr11 + 62761852 62761852 62761852 TGCACCCGCGCTACTTCGGCCCCAACTTGCTCAACACGGTGAAGCAGAAGCTCTTCACCGAGGTG TGCACCCGCGCTACTTCGGCCCCAACTTGCTCGACACGGTGAAGCAGAAGCTCTTCACCGAGGTG A G POLR2G Ensembl:ENSG00000168002 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62761766..62761875 26863196 MeRIP-seq:(Medium) rs1565182337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184980,Human_RBP_ID_9321470,Human_RBP_ID_22433031,Human_RBP_ID_26803665 Human_Splice_Rec_1249298,Human_Splice_Rec_1249299,Human_Splice_Rec_1249306,Human_Splice_Rec_1249307,Human_Splice_Rec_1249320,Human_Splice_Rec_1249321,Human_Splice_Rec_1249334,Human_Splice_Rec_1249348,Human_Splice_Rec_1249359,Human_Splice_Rec_1249371 RMVar_hsa_circ_26035,RMVar_hsa_circ_101487,RMVar_hsa_circ_150259,RMVar_hsa_circ_111234,RMVar_hsa_circ_150260 56504 RMVar_ID_56504 Human_SNP_ID_469287175 m1A Human chr11 + 62771436 62771436 62771436 TGAGTGTGAGCTCGTGAGTGGGCGCCGCCGCCACCGCCCCCGCCGCCGTCGTCTCGGTAGCAGCC TGAGTGTGAGCTCGTGAGTGGGCGCCGCCGCCCCCGCCCCCGCCGCCGTCGTCTCGGTAGCAGCC A C TAF6L Ensembl:ENSG00000162227 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62771396..62772051 26863196 MeRIP-seq:(Medium) rs915711924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416569 Human_Splice_Rec_1249391,Human_Splice_Rec_1249395,Human_Splice_Rec_1249405,Human_Splice_Rec_1249425,Human_Splice_Rec_1249439 56505 RMVar_ID_56505 Human_SNP_ID_469287183 m1A Human chr11 - 62771452 62771452 62771452 ACCCCGGCGTGGCGAAGGCTGCTACCGAGACGACGGCGGCGGGGGCGGTGGCGGCGGCGCCCACT ACCCCGGCGTGGCGAAGGCTGCTACCGAGACGTCGGCGGCGGGGGCGGTGGCGGCGGCGCCCACT T A AP001160.2 Ensembl:ENSG00000267811 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62771401..62771779 26863196 MeRIP-seq:(Medium) rs1018173240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150267 56506 RMVar_ID_56506 Human_SNP_ID_469287184 m1A Human chr11 - 62771452 62771452 62771452 ACCCCGGCGTGGCGAAGGCTGCTACCGAGACGACGGCGGCGGGGGCGGTGGCGGCGGCGCCCACT ACCCCGGCGTGGCGAAGGCTGCTACCGAGACGGCGGCGGCGGGGGCGGTGGCGGCGGCGCCCACT T C AP001160.2 Ensembl:ENSG00000267811 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62771401..62771779 26863196 MeRIP-seq:(Medium) rs1018173240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150267 56507 RMVar_ID_56507 Human_SNP_ID_469289140 m1A Human chr11 + 62778214 62778214 62778214 AGTGGTGATGGGCTGGCTGGTGGAAGAGGCAGAACTTGGAGGGGTAGGCGGTACTCTAAGGGGCA AGTGGTGATGGGCTGGCTGGTGGAAGAGGCAGTACTTGGAGGGGTAGGCGGTACTCTAAGGGGCA A T TAF6L Ensembl:ENSG00000162227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62778209..62778279 26863196 MeRIP-seq:(Medium) rs551714648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305738 56508 RMVar_ID_56508 Human_SNP_ID_469292368 m1A Human chr11 - 62787484 62787484 62787484 TCATCGCCGCGGCCGCCACGGCCCCGCACAGGAAGGCGGCAGCAAAGAGCGCAAGCTCGACGCGC TCATCGCCGCGGCCGCCACGGCCCCGCACAGGTAGGCGGCAGCAAAGAGCGCAAGCTCGACGCGC T A TMEM223 Ensembl:ENSG00000168569 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62787434..62787514 26863196 MeRIP-seq:(Medium) rs1276875283 Functional Loss SNV dbSNP153 33..33 33 - - - 56509 RMVar_ID_56509 Human_SNP_ID_469294164 m1A Human chr11 - 62791903 62791903 62791903 CACCTGCCGGCCCCTGCAAGGCACGACGCTGCAACGGGATGTGCTGCTCTTTGAGCATGATCGGG CACCTGCCGGCCCCTGCAAGGCACGACGCTGCGACGGGATGTGCTGCTCTTTGAGCATGATCGGG T C TMEM223 Ensembl:ENSG00000168569 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62791868..62791965 26863196 MeRIP-seq:(Medium) rs200911666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4167612,Human_RBP_ID_22163636 56510 RMVar_ID_56510 Human_SNP_ID_469294177 m1A Human chr11 + 62791921 62791921 62791921 GCAGCACATCCCGTTGCAGCGTCGTGCCTTGCAGGGGCCGGCAGGTGAGCAGGGGCCGCAGCACG GCAGCACATCCCGTTGCAGCGTCGTGCCTTGCGGGGGCCGGCAGGTGAGCAGGGGCCGCAGCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62791872..62791955 26863196 MeRIP-seq:(Medium) rs1292502064 Functional Loss SNV dbSNP153 33..33 33 - - - 56511 RMVar_ID_56511 Human_SNP_ID_469306280 m1A Human chr11 + 62833001 62833001 62833001 CAGGCCGCTTCTTCTTTCTCCGTCTCGTTTGGAGAGCTCCTTGGGGCTGCTCCAAACCCGAGAGC CAGGCCGCTTCTTCTTTCTCCGTCTCGTTTGGCGAGCTCCTTGGGGCTGCTCCAAACCCGAGAGC A C AP001160.1 Ensembl:ENSG00000256690 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62832910..62833010 32194978 MeRIP-seq:(Medium) rs756320838 Functional Loss SNV dbSNP153 33..33 33 - - - 56512 RMVar_ID_56512 Human_SNP_ID_469306283 m1A Human chr11 - 62833009 62833009 62833009 AAGCGGAAGCTCTCGGGTTTGGAGCAGCCCCAAGGAGCTCTCCAAACGAGACGGAGAAAGAAGAA AAGCGGAAGCTCTCGGGTTTGGAGCAGCCCCAGGGAGCTCTCCAAACGAGACGGAGAAAGAAGAA T C WDR74 Ensembl:ENSG00000133316 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62832962..62833073 26863196 MeRIP-seq:(Medium) rs780356662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4167738,Human_RBP_ID_9362390,Human_RBP_ID_17798344,Human_RBP_ID_18973880,Human_RBP_ID_26320028 Human_Splice_Rec_1249885 RMVar_hsa_circ_122229,RMVar_hsa_circ_150291 56513 RMVar_ID_56513 Human_SNP_ID_469306723 m1A Human chr11 - 62834308 62834308 62834308 CATCCTCAGCTCAGTGATTGTGGGAAACACTCATGGGCAGCTGGCAGAAATTGACCTTCGGCAAG CATCCTCAGCTCAGTGATTGTGGGAAACACTCGTGGGCAGCTGGCAGAAATTGACCTTCGGCAAG T C WDR74 Ensembl:ENSG00000133316 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62834278..62834433 32194978 MeRIP-seq:(Medium) rs1407741239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399277,Human_RBP_ID_865091,Human_RBP_ID_987714,Human_RBP_ID_1780686,Human_RBP_ID_3939262,Human_RBP_ID_4167747,Human_RBP_ID_5341441,Human_RBP_ID_8354154,Human_RBP_ID_8770653,Human_RBP_ID_18972127 Human_Splice_Rec_1249900,Human_Splice_Rec_1249901,Human_Splice_Rec_1249918,Human_Splice_Rec_1249919,Human_Splice_Rec_1249940,Human_Splice_Rec_1249941,Human_Splice_Rec_1249962,Human_Splice_Rec_1249963,Human_Splice_Rec_1249984,Human_Splice_Rec_1249985,Human_Splice_Rec_1249992,Human_Splice_Rec_1249993,Human_Splice_Rec_1250000,Human_Splice_Rec_1250001,Human_Splice_Rec_1250014,Human_Splice_Rec_1250015 RMVar_hsa_circ_122229,RMVar_hsa_circ_150292,RMVar_hsa_circ_78239,RMVar_hsa_circ_122119,RMVar_hsa_circ_150291,RMVar_hsa_circ_150293,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_368007,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295 56514 RMVar_ID_56514 Human_SNP_ID_469306831 m1A Human chr11 - 62834529 62834529 62834529 AGGATACTTTTGTGATGCTTCAGCCTTCCTCTAGGTCCGTGTTTATGATCCAGCATCCCCCCAGC AGGATACTTTTGTGATGCTTCAGCCTTCCTCTGGGTCCGTGTTTATGATCCAGCATCCCCCCAGC T C WDR74 Ensembl:ENSG00000133316 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62834482..62834590 26863196 MeRIP-seq:(Medium) rs1425808443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18609872 RMVar_hsa_circ_122229,RMVar_hsa_circ_150292,RMVar_hsa_circ_78239,RMVar_hsa_circ_122119,RMVar_hsa_circ_150291,RMVar_hsa_circ_150293,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_368007,RMVar_hsa_circ_150294,RMVar_hsa_circ_93077,RMVar_hsa_circ_150295,RMVar_hsa_circ_150296 56515 RMVar_ID_56515 Human_SNP_ID_469309712 m1A Human chr11 - 62841702 62841691 62841703 TCCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCA TCCGAGGACAATATATTAAATGGATTTTTGG____________GAATAGGAGCTTGCTCCGTCCA CCATCTCCTATTT C WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:62841651..62841798;chr11:62841651..62841725 26863196 MeRIP-seq:(Medium) rs1213800832 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9321480,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56516 RMVar_ID_56516 Human_SNP_ID_469309744 m1A Human chr11 - 62841701 62841701 62841701 CCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCAC CCGAGGACAATATATTAAATGGATTTTTGGAATTAGGAGATGGAATAGGAGCTTGCTCCGTCCAC T A WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62841651..62841814 26863196 MeRIP-seq:(Medium) rs77654912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56517 RMVar_ID_56517 Human_SNP_ID_469309745 m1A Human chr11 - 62841701 62841701 62841701 CCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCAC CCGAGGACAATATATTAAATGGATTTTTGGAAGTAGGAGATGGAATAGGAGCTTGCTCCGTCCAC T C WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62841651..62841814 26863196 MeRIP-seq:(Medium) rs77654912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56518 RMVar_ID_56518 Human_SNP_ID_469309746 m1A Human chr11 - 62841701 62841701 62841701 CCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCAC CCGAGGACAATATATTAAATGGATTTTTGGAACTAGGAGATGGAATAGGAGCTTGCTCCGTCCAC T G WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62841651..62841814 26863196 MeRIP-seq:(Medium) rs77654912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56519 RMVar_ID_56519 Human_SNP_ID_469309747 m1A Human chr11 - 62841702 62841702 62841702 TCCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCA TCCGAGGACAATATATTAAATGGATTTTTGGAGATAGGAGATGGAATAGGAGCTTGCTCCGTCCA T C WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:62841651..62841798;chr11:62841651..62841725 26863196 MeRIP-seq:(Medium) rs75829596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9321480,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56520 RMVar_ID_56520 Human_SNP_ID_469309748 m1A Human chr11 - 62841702 62841702 62841702 TCCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCA TCCGAGGACAATATATTAAATGGATTTTTGGACATAGGAGATGGAATAGGAGCTTGCTCCGTCCA T G WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:62841651..62841798;chr11:62841651..62841725 26863196 MeRIP-seq:(Medium) rs75829596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9321480,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 56521 RMVar_ID_56521 Human_SNP_ID_469313452 m1A Human chr11 - 62852683 62852661 62852683 AATCCAATAAGAACTTTTTTTTTTACCTCTGCAGGAATCTGTCTTGGAGGACATCAGAAGGTGAA AATCCAATAAGAACTTTTTTTTTTACCTCTGC______________________CAGAAGGTGAA GATGTCCTCCAAGACAGATTCCT G SNHG1 Ensembl:ENSG00000255717 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62852679..62852994 32194978 MeRIP-seq:(Medium) rs1484660062 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_1780692,Human_RBP_ID_2273460,Human_RBP_ID_4187103,Human_RBP_ID_22569320,Human_RBP_ID_24557083,Human_RBP_ID_24893273 Human_Splice_Rec_1250159 RMVar_hsa_circ_7520,RMVar_hsa_circ_117237,RMVar_hsa_circ_121910,RMVar_hsa_circ_119149,RMVar_hsa_circ_150305,RMVar_hsa_circ_100429,RMVar_hsa_circ_102359,RMVar_hsa_circ_150307,RMVar_hsa_circ_93699,RMVar_hsa_circ_150306,RMVar_hsa_circ_150303,RMVar_hsa_circ_150304,RMVar_hsa_circ_150302 56522 RMVar_ID_56522 Human_SNP_ID_469313458 m1A Human chr11 - 62852683 62852683 62852683 AATCCAATAAGAACTTTTTTTTTTACCTCTGCAGGAATCTGTCTTGGAGGACATCAGAAGGTGAA AATCCAATAAGAACTTTTTTTTTTACCTCTGCGGGAATCTGTCTTGGAGGACATCAGAAGGTGAA T C SNHG1 Ensembl:ENSG00000255717 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62852679..62852994 32194978 MeRIP-seq:(Medium) rs1319501016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780692,Human_RBP_ID_2273460,Human_RBP_ID_4187103,Human_RBP_ID_22569320,Human_RBP_ID_24557083,Human_RBP_ID_24893273 Human_Splice_Rec_1250159 RMVar_hsa_circ_7520,RMVar_hsa_circ_117237,RMVar_hsa_circ_121910,RMVar_hsa_circ_119149,RMVar_hsa_circ_150305,RMVar_hsa_circ_100429,RMVar_hsa_circ_102359,RMVar_hsa_circ_150307,RMVar_hsa_circ_93699,RMVar_hsa_circ_150306,RMVar_hsa_circ_150303,RMVar_hsa_circ_150304,RMVar_hsa_circ_150302 56523 RMVar_ID_56523 Human_SNP_ID_469314779 m1A Human chr11 - 62855617 62855617 62855617 GGGCCGTGTAGGTCCCCCTTCCTATGATGAGGACCTTTTCACAGACCTGTACTGAGCTCCGTGAG GGGCCGTGTAGGTCCCCCTTCCTATGATGAGGGCCTTTTCACAGACCTGTACTGAGCTCCGTGAG T C SNHG1,SNORD25 Ensembl:ENSG00000255717,Ensembl:ENSG00000275043 lincRNA,snoRNA exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62855567..62855766 32194978 MeRIP-seq:(Medium) rs1432234580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399334,Human_RBP_ID_1063915,Human_RBP_ID_1079749,Human_RBP_ID_1162513,Human_RBP_ID_1354670,Human_RBP_ID_1458417,Human_RBP_ID_1780736,Human_RBP_ID_2273539,Human_RBP_ID_3377269,Human_RBP_ID_5093693,Human_RBP_ID_5169675,Human_RBP_ID_5246170,Human_RBP_ID_5460557,Human_RBP_ID_5489953,Human_RBP_ID_5552089,Human_RBP_ID_6083093,Human_RBP_ID_8061958,Human_RBP_ID_8246477,Human_RBP_ID_8354257,Human_RBP_ID_8770700,Human_RBP_ID_9004702,Human_RBP_ID_9274993,Human_RBP_ID_11660610,Human_RBP_ID_17682305,Human_RBP_ID_17798389,Human_RBP_ID_18198726,Human_RBP_ID_18206126,Human_RBP_ID_18432926,Human_RBP_ID_18510725,Human_RBP_ID_18525924,Human_RBP_ID_18609954,Human_RBP_ID_23511465,Human_RBP_ID_26747670,Human_RBP_ID_27154198,Human_RBP_ID_27203700,Human_RBP_ID_27413323,Human_RBP_ID_27556995,Human_RBP_ID_27618690 RMVar_hsa_circ_117237,RMVar_hsa_circ_121910,RMVar_hsa_circ_93699,RMVar_hsa_circ_150303,RMVar_hsa_circ_150304,RMVar_hsa_circ_150302,RMVar_hsa_circ_106201,RMVar_hsa_circ_79860,RMVar_hsa_circ_150313,RMVar_hsa_circ_100895,RMVar_hsa_circ_87255,RMVar_hsa_circ_150316,RMVar_hsa_circ_150317,RMVar_hsa_circ_150322,RMVar_hsa_circ_78571,RMVar_hsa_circ_150323 56524 RMVar_ID_56524 Human_SNP_ID_469315147 m1A Human chr11 - 62856252 62856252 62856252 AGGCTGTAGCTCCATGGAGGCGGATCCTGCACACAGGTTTGGGGTGTGTGGGCAAGGGGCAGCTC AGGCTGTAGCTCCATGGAGGCGGATCCTGCACTCAGGTTTGGGGTGTGTGGGCAAGGGGCAGCTC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62856201..62870764 32194978 MeRIP-seq:(Medium) rs201599156 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_156 56525 RMVar_ID_56525 Human_SNP_ID_469315613 m1A Human chr11 - 62857777 62857777 62857777 TCCCGACTGCCATTCCCACACACAACCTCCCCAGCCTTGTCTGTCTACTCTGGGCCATCTTGATT TCCCGACTGCCATTCCCACACACAACCTCCCCGGCCTTGTCTGTCTACTCTGGGCCATCTTGATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62857776..62857913 26863196 MeRIP-seq:(Medium) rs955564304 Functional Loss SNV dbSNP153 33..33 33 - - - 56526 RMVar_ID_56526 Human_SNP_ID_469319009 m1A Human chr11 - 62870732 62870725 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAA_______TAATAATAATAATAATGTATAAAGTA ATTTTTTT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs754127613 Functional Loss DEL dbSNP153 33..39 33 - - - 56527 RMVar_ID_56527 Human_SNP_ID_469319010 m1A Human chr11 - 62870732 62870725 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAA______ATAATAATAATAATAATGTATAAAGTA ATTTTTTT AT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs754127613 Functional Loss DEL dbSNP153 33..38 33 - - - 56528 RMVar_ID_56528 Human_SNP_ID_469319011 m1A Human chr11 - 62870732 62870725 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAA___AAAATAATAATAATAATAATGTATAAAGTA ATTTTTTT ATTTT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs754127613 Functional Loss DEL dbSNP153 33..35 33 - - - 56529 RMVar_ID_56529 Human_SNP_ID_469319012 m1A Human chr11 - 62870732 62870725 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAA__AAAAATAATAATAATAATAATGTATAAAGTA ATTTTTTT ATTTTT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs754127613 Functional Loss DEL dbSNP153 33..34 33 - - - 56530 RMVar_ID_56530 Human_SNP_ID_469319013 m1A Human chr11 - 62870732 62870725 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAA_AAAAAATAATAATAATAATAATGTATAAAGTA ATTTTTTT ATTTTTT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs754127613 Functional Loss DEL dbSNP153 33..33 33 - - - 56531 RMVar_ID_56531 Human_SNP_ID_469319026 m1A Human chr11 - 62870732 62870732 62870732 AACACAGTGAGACCCCAACTCTACAAAAAAAAAAAAAAATAATAATAATAATAATGTATAAAGTA AACACAGTGAGACCCCAACTCTACAAAAAAAATAAAAAATAATAATAATAATAATGTATAAAGTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62870726..62870750 26863196 MeRIP-seq:(Medium) rs1250277197 Functional Loss SNV dbSNP153 33..33 33 - - - 56532 RMVar_ID_56532 Human_SNP_ID_469319370 m1A Human chr11 + 62871537 62871537 62871537 GCTGGGATTACAGGCGTGAGCCACTGTGCCCAACCATACTTTATATAATATTATTATTATTATTA GCTGGGATTACAGGCGTGAGCCACTGTGCCCAGCCATACTTTATATAATATTATTATTATTATTA A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62871533..62871721 26863196 MeRIP-seq:(Medium) rs915170448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92726,RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326,RMVar_hsa_circ_150329 56533 RMVar_ID_56533 Human_SNP_ID_469321669 m1A Human chr11 + 62880986 62880986 62880986 GAGGGTCCAGGTAGGGGTTGAGCCACCATCTGACCGCAAGCTGCGTCGTGTCGCCGGTTCTGCAG GAGGGTCCAGGTAGGGGTTGAGCCACCATCTGGCCGCAAGCTGCGTCGTGTCGCCGGTTCTGCAG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62880926..62881178 26863196 MeRIP-seq:(Medium) rs374326797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226948,Human_RBP_ID_807361,Human_RBP_ID_869081,Human_RBP_ID_1235294,Human_RBP_ID_1458430,Human_RBP_ID_4167886,Human_RBP_ID_8354284,Human_RBP_ID_11661143,Human_RBP_ID_18609960,Human_RBP_ID_22571151,Human_RBP_ID_22641380,Human_RBP_ID_26893158 Human_Splice_Rec_1250805 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 56534 RMVar_ID_56534 Human_SNP_ID_469321673 m1A Human chr11 + 62880991 62880991 62880991 TCCAGGTAGGGGTTGAGCCACCATCTGACCGCAAGCTGCGTCGTGTCGCCGGTTCTGCAGGCACC TCCAGGTAGGGGTTGAGCCACCATCTGACCGCCAGCTGCGTCGTGTCGCCGGTTCTGCAGGCACC A C SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:62880926..62881027 26863410 MeRIP-seq:(Medium) rs1229016529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226948,Human_RBP_ID_807361,Human_RBP_ID_869081,Human_RBP_ID_1235294,Human_RBP_ID_1458430,Human_RBP_ID_4167889,Human_RBP_ID_5165617,Human_RBP_ID_8354284,Human_RBP_ID_11661143,Human_RBP_ID_18609960,Human_RBP_ID_22571151,Human_RBP_ID_22641380,Human_RBP_ID_27413336 Human_Splice_Rec_1250805 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 56535 RMVar_ID_56535 Human_SNP_ID_469321692 m1A Human chr11 + 62881052 62881052 62881052 CACCATGAGCCAGGACACCGAGGTGGATATGAAGGAGGTGGAGCTGAATGAGTTAGAGCCCGAGA CACCATGAGCCAGGACACCGAGGTGGATATGACGGAGGTGGAGCTGAATGAGTTAGAGCCCGAGA A C SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:62880952..62881137 26863410 MeRIP-seq:(Medium) rs772982523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1458430,Human_RBP_ID_1780740,Human_RBP_ID_2273563,Human_RBP_ID_3377283,Human_RBP_ID_4167894,Human_RBP_ID_5549550,Human_RBP_ID_6083151,Human_RBP_ID_8354286,Human_RBP_ID_11661143,Human_RBP_ID_18609961,Human_RBP_ID_22434534,Human_RBP_ID_23511496,Human_RBP_ID_27413337 Human_Splice_Rec_1250702,Human_Splice_Rec_1250724,Human_Splice_Rec_1250742,Human_Splice_Rec_1250762,Human_Splice_Rec_1250784,Human_Splice_Rec_1250788,Human_Splice_Rec_1250805 Human_miRNA_ID_2016103,Human_miRNA_ID_2195488 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150334,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_150333 56536 RMVar_ID_56536 Human_SNP_ID_469321695 m1A Human chr11 - 62881073 62881059 62881074 ACGCCGCGTTCATCGGCTGCTTCTCGGGCTCTAACTCATTCAGCTCCACCTCCTTCATATCCACC ACGCCGCGTTCATCGGCTGCTTCTCGGGCTC_______________CACCTCCTTCATATCCACC GGAGCTGAATGAGTTA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:62880901..62881148 26863196 MeRIP-seq:(Medium) rs1372908044 Functional Loss DEL dbSNP153 32..46 33 - - - 56537 RMVar_ID_56537 Human_SNP_ID_469321750 m1A Human chr11 + 62881175 62881163 62881175 TGGTCTGGTGAAGATCAAGGTGGCGGAAGACGAGGCGGAGGCGGCAGCCGCGGCTAAGTTCACGG TGGTCTGGTGAAGATCAAGGT____________GGCGGAGGCGGCAGCCGCGGCTAAGTTCACGG TGGCGGAAGACGA T SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:62881151..62881175 26863196 MeRIP-seq:(Medium) rs1232285250 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_750206,Human_RBP_ID_807574,Human_RBP_ID_3939263,Human_RBP_ID_4167903,Human_RBP_ID_19696416,Human_RBP_ID_22433687,Human_RBP_ID_26318558 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150334,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_150333 56538 RMVar_ID_56538 Human_SNP_ID_469321761 m1A Human chr11 + 62881175 62881175 62881175 TGGTCTGGTGAAGATCAAGGTGGCGGAAGACGAGGCGGAGGCGGCAGCCGCGGCTAAGTTCACGG TGGTCTGGTGAAGATCAAGGTGGCGGAAGACGTGGCGGAGGCGGCAGCCGCGGCTAAGTTCACGG A T SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:62881151..62881175 26863196 MeRIP-seq:(Medium) rs762735137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750206,Human_RBP_ID_807574,Human_RBP_ID_3939263,Human_RBP_ID_4167903,Human_RBP_ID_19696416,Human_RBP_ID_22433687,Human_RBP_ID_26318558 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150334,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_150333 56539 RMVar_ID_56539 Human_SNP_ID_469321844 m1A Human chr11 - 62881328 62881328 62881328 GTAGCTCGCGACAACGCGGCGCTCGCACGATTATGACCACGGCACCAGCAAGCATGCCGAGCCAG GTAGCTCGCGACAACGCGGCGCTCGCACGATTTTGACCACGGCACCAGCAAGCATGCCGAGCCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:62881151..62881450 26863410 MeRIP-seq:(Medium) rs1186731133 Functional Loss SNV dbSNP153 33..33 33 - - - 56540 RMVar_ID_56540 Human_SNP_ID_469321878 m1A Human chr11 + 62881412 62881412 62881412 CACGGGCGCCCTCTACCGCATCGGCGACCTTCAGGCCTTCCAGGGCCACGGCGCGGGCAACCTGG CACGGGCGCCCTCTACCGCATCGGCGACCTTCGGGCCTTCCAGGGCCACGGCGCGGGCAACCTGG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62880951..62881695 32194978 MeRIP-seq:(Medium) rs779945959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226951,Human_RBP_ID_1265092,Human_RBP_ID_17798397,Human_RBP_ID_22433691,Human_RBP_ID_22755463,Human_RBP_ID_27836339 Human_Splice_Rec_1250703,Human_Splice_Rec_1250725,Human_Splice_Rec_1250743,Human_Splice_Rec_1250763,Human_Splice_Rec_1250785,Human_Splice_Rec_1250789 Human_miRNA_ID_2027313,Human_miRNA_ID_2427140,Human_miRNA_ID_2727826 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150334,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_150333 56541 RMVar_ID_56541 Human_SNP_ID_469322130 m1A Human chr11 + 62882066 62882056 62882067 TTGACAGTCTCTTGCAATCGGCTAAAAAAAAGAGTGGGTATCCTGGGGTTCCCAAGGAAACAGCT TTGACAGTCTCTTGCAATCGGCT___________TGGGTATCCTGGGGTTCCCAAGGAAACAGCT TAAAAAAAAGAG T SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62882026..62882075 32194978 MeRIP-seq:(Medium) rs770255364 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_807576,Human_RBP_ID_869352,Human_RBP_ID_5342460,Human_RBP_ID_9362396,Human_RBP_ID_17232645,Human_RBP_ID_17668708,Human_RBP_ID_19049620,Human_RBP_ID_22471209,Human_RBP_ID_22753655,Human_RBP_ID_27203718 Human_Splice_Rec_1250705,Human_Splice_Rec_1250727,Human_Splice_Rec_1250745,Human_Splice_Rec_1250765,Human_Splice_Rec_1250791,Human_Splice_Rec_1250811,Human_Splice_Rec_1250821,Human_Splice_Rec_1250827,Human_Splice_Rec_1250845,Human_Splice_Rec_1250863,Human_Splice_Rec_1250869,Human_Splice_Rec_1250883 RMVar_hsa_circ_110846,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150334,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_356384,RMVar_hsa_circ_150333,RMVar_hsa_circ_372623,RMVar_hsa_circ_301056,RMVar_hsa_circ_150335,RMVar_hsa_circ_1918,RMVar_hsa_circ_109220,RMVar_hsa_circ_150337,RMVar_hsa_circ_150338,RMVar_hsa_circ_150336 56542 RMVar_ID_56542 Human_SNP_ID_469322816 m1A Human chr11 + 62884661 62884661 62884661 TAGGATGCATCCTCATTCTTGGCTGAGTGGCAAAATATCACCAAGGGCTTCAGTGAAGACAGGTG TAGGATGCATCCTCATTCTTGGCTGAGTGGCACAATATCACCAAGGGCTTCAGTGAAGACAGGTG A C SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62884451..62885350 32194978 MeRIP-seq:(Medium) rs910760207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865100,Human_RBP_ID_987748,Human_RBP_ID_1458460,Human_RBP_ID_1780750,Human_RBP_ID_3939268,Human_RBP_ID_4167935,Human_RBP_ID_5341472,Human_RBP_ID_8770706,Human_RBP_ID_11661311,Human_RBP_ID_17798402,Human_RBP_ID_18251349,Human_RBP_ID_22471215,Human_RBP_ID_22569334,Human_RBP_ID_22641390,Human_RBP_ID_22753659,Human_RBP_ID_22791106,Human_RBP_ID_23511521,Human_RBP_ID_26775616 Human_Splice_Rec_1250710,Human_Splice_Rec_1250711,Human_Splice_Rec_1250732,Human_Splice_Rec_1250733,Human_Splice_Rec_1250750,Human_Splice_Rec_1250751,Human_Splice_Rec_1250770,Human_Splice_Rec_1250771,Human_Splice_Rec_1250796,Human_Splice_Rec_1250797,Human_Splice_Rec_1250816,Human_Splice_Rec_1250817,Human_Splice_Rec_1250836,Human_Splice_Rec_1250837,Human_Splice_Rec_1250852,Human_Splice_Rec_1250853,Human_Splice_Rec_1250874,Human_Splice_Rec_1250875,Human_Splice_Rec_1250888,Human_Splice_Rec_1250889,Human_Splice_Rec_1250898,Human_Splice_Rec_1250899,Human_Splice_Rec_1250906,Human_Splice_Rec_1250907,Human_Splice_Rec_1250912,Human_Splice_Rec_1250913,Human_Splice_Rec_1250922,Human_Splice_Rec_1250923 Human_miRNA_ID_2001786,Human_miRNA_ID_2001787,Human_miRNA_ID_2003170,Human_miRNA_ID_2003171,Human_miRNA_ID_2364248,Human_miRNA_ID_2364249 RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_356384,RMVar_hsa_circ_150333,RMVar_hsa_circ_372623,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_1918,RMVar_hsa_circ_150337,RMVar_hsa_circ_150338,RMVar_hsa_circ_120976,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_284508,RMVar_hsa_circ_150341,RMVar_hsa_circ_150342,RMVar_hsa_circ_150340,RMVar_hsa_circ_97274,RMVar_hsa_circ_150345 56543 RMVar_ID_56543 Human_SNP_ID_469322817 m1A Human chr11 + 62884661 62884661 62884661 TAGGATGCATCCTCATTCTTGGCTGAGTGGCAAAATATCACCAAGGGCTTCAGTGAAGACAGGTG TAGGATGCATCCTCATTCTTGGCTGAGTGGCAGAATATCACCAAGGGCTTCAGTGAAGACAGGTG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62884451..62885350 32194978 MeRIP-seq:(Medium) rs910760207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865100,Human_RBP_ID_987748,Human_RBP_ID_1458460,Human_RBP_ID_1780750,Human_RBP_ID_3939268,Human_RBP_ID_4167935,Human_RBP_ID_5341472,Human_RBP_ID_8770706,Human_RBP_ID_11661311,Human_RBP_ID_17798402,Human_RBP_ID_18251349,Human_RBP_ID_22471215,Human_RBP_ID_22569334,Human_RBP_ID_22641390,Human_RBP_ID_22753659,Human_RBP_ID_22791106,Human_RBP_ID_23511521,Human_RBP_ID_26775616 Human_Splice_Rec_1250710,Human_Splice_Rec_1250711,Human_Splice_Rec_1250732,Human_Splice_Rec_1250733,Human_Splice_Rec_1250750,Human_Splice_Rec_1250751,Human_Splice_Rec_1250770,Human_Splice_Rec_1250771,Human_Splice_Rec_1250796,Human_Splice_Rec_1250797,Human_Splice_Rec_1250816,Human_Splice_Rec_1250817,Human_Splice_Rec_1250836,Human_Splice_Rec_1250837,Human_Splice_Rec_1250852,Human_Splice_Rec_1250853,Human_Splice_Rec_1250874,Human_Splice_Rec_1250875,Human_Splice_Rec_1250888,Human_Splice_Rec_1250889,Human_Splice_Rec_1250898,Human_Splice_Rec_1250899,Human_Splice_Rec_1250906,Human_Splice_Rec_1250907,Human_Splice_Rec_1250912,Human_Splice_Rec_1250913,Human_Splice_Rec_1250922,Human_Splice_Rec_1250923 Human_miRNA_ID_2001786,Human_miRNA_ID_2001787,Human_miRNA_ID_2003170,Human_miRNA_ID_2003171,Human_miRNA_ID_2364248,Human_miRNA_ID_2364249 RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_368262,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_356384,RMVar_hsa_circ_150333,RMVar_hsa_circ_372623,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_1918,RMVar_hsa_circ_150337,RMVar_hsa_circ_150338,RMVar_hsa_circ_120976,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_284508,RMVar_hsa_circ_150341,RMVar_hsa_circ_150342,RMVar_hsa_circ_150340,RMVar_hsa_circ_97274,RMVar_hsa_circ_150345 56544 RMVar_ID_56544 Human_SNP_ID_469323980 m1A Human chr11 - 62888533 62888533 62888533 GGCTGGCGCTGGCAGGCAGGTCGGAGGCCTGCAGTCCAGCCGAGAGGCCCACATCCCCAAAGTTA GGCTGGCGCTGGCAGGCAGGTCGGAGGCCTGCGGTCCAGCCGAGAGGCCCACATCCCCAAAGTTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62888482..62888810 26863196 MeRIP-seq:(Medium) rs893338654 Functional Loss SNV dbSNP153 33..33 33 - - - 56545 RMVar_ID_56545 Human_SNP_ID_469514107 m1A Human chr11 - 63570695 63570695 63570695 AAAAGGGGAAGACAATACAAAGATATGAGCAAAAATAAATGAAGAAAAACAAGCATATAAAAGAG AAAAGGGGAAGACAATACAAAGATATGAGCAAGAATAAATGAAGAAAAACAAGCATATAAAAGAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63570648..63570805 26863196 MeRIP-seq:(Medium) rs964598176 Functional Loss SNV dbSNP153 33..33 33 - - - 56546 RMVar_ID_56546 Human_SNP_ID_469514108 m1A Human chr11 - 63570700 63570700 63570700 ACAGAAAAAGGGGAAGACAATACAAAGATATGAGCAAAAATAAATGAAGAAAAACAAGCATATAA ACAGAAAAAGGGGAAGACAATACAAAGATATGGGCAAAAATAAATGAAGAAAAACAAGCATATAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63570650..63570831 26863196 MeRIP-seq:(Medium) rs1404292836 Functional Loss SNV dbSNP153 33..33 33 - - - 56547 RMVar_ID_56547 Human_SNP_ID_469519033 m1A Human chr11 + 63590176 63590176 63590176 GCTCGCAGTTCTCACTGGTCAGCTTGTAGAGCACCTCCTGCCCCACCAGCTCCTCCGCCCGCTGG GCTCGCAGTTCTCACTGGTCAGCTTGTAGAGCCCCTCCTGCCCCACCAGCTCCTCCGCCCGCTGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:63590126..63608492 32194978 MeRIP-seq:(Medium) rs78097659 Functional Loss SNV dbSNP153 33..33 33 - - - 56548 RMVar_ID_56548 Human_SNP_ID_469519040 m1A Human chr11 - 63590194 63590194 63590194 GCCCTGCAGCAAAATCATCCAGCGGGCGGAGGAGCTGGTGGGGCAGGAGGTGCTCTACAAGCTGA GCCCTGCAGCAAAATCATCCAGCGGGCGGAGGTGCTGGTGGGGCAGGAGGTGCTCTACAAGCTGA T A PLAAT3 Ensembl:ENSG00000176485 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63590145..63590397 26863196 MeRIP-seq:(Medium) rs1467752478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1251551,Human_Splice_Rec_1251557,Human_Splice_Rec_1251565,Human_Splice_Rec_1251571 Human_miRNA_ID_2016104,Human_miRNA_ID_2151497,Human_miRNA_ID_2419968 RMVar_hsa_circ_305442,RMVar_hsa_circ_309211,RMVar_hsa_circ_150351 56549 RMVar_ID_56549 Human_SNP_ID_469519050 m1A Human chr11 - 63590206 63590206 63590206 GTACTCGCCGCTGCCCTGCAGCAAAATCATCCAGCGGGCGGAGGAGCTGGTGGGGCAGGAGGTGC GTACTCGCCGCTGCCCTGCAGCAAAATCATCCCGCGGGCGGAGGAGCTGGTGGGGCAGGAGGTGC T G PLAAT3 Ensembl:ENSG00000176485 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63590155..63590412 26863196 MeRIP-seq:(Medium) rs1393740596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2000221 RMVar_hsa_circ_305442,RMVar_hsa_circ_309211,RMVar_hsa_circ_150351 56550 RMVar_ID_56550 Human_SNP_ID_469521039 m1A Human chr11 - 63598165 63598164 63598165 GCTCCCTCTAACAGCCCTGTTCTTGGTTTTGCAGCCAGAGCCTAAGCCTGGAGACCTGATTGAGA GCTCCCTCTAACAGCCCTGTTCTTGGTTTTGC_GCCAGAGCCTAAGCCTGGAGACCTGATTGAGA CT C PLAAT3 Ensembl:ENSG00000176485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63598115..63608492 26863196 MeRIP-seq:(Medium) rs1565253448 Functional Loss DEL dbSNP153 33..33 33 - - - 56551 RMVar_ID_56551 Human_SNP_ID_469524910 m1A Human chr11 + 63614032 63614032 63614032 AATGGGCGCACGCATCTTCCCTCGCGGTGTGGACCCTCAAGGCCAGGCTCGATTTCGCTGCGTAG AATGGGCGCACGCATCTTCCCTCGCGGTGTGGGCCCTCAAGGCCAGGCTCGATTTCGCTGCGTAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63614001..63614475 26863196 MeRIP-seq:(Medium) rs559177177 Functional Loss SNV dbSNP153 33..33 33 - - - 56552 RMVar_ID_56552 Human_SNP_ID_469524928 m1A Human chr11 - 63614058 63614058 63614058 ATCCCTGCTCCCCCTGCCTCAGACATCTACGCAGCGAAATCGAGCCTGGCCTTGAGGGTCCACAC ATCCCTGCTCCCCCTGCCTCAGACATCTACGCTGCGAAATCGAGCCTGGCCTTGAGGGTCCACAC T A PLAAT3 Ensembl:ENSG00000176485 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63614008..63614108 26863196 MeRIP-seq:(Medium) rs760182104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1251547,Human_Splice_Rec_1251560,Human_Splice_Rec_1251561,Human_Splice_Rec_1251567 56553 RMVar_ID_56553 Human_SNP_ID_469524929 m1A Human chr11 - 63614058 63614058 63614058 ATCCCTGCTCCCCCTGCCTCAGACATCTACGCAGCGAAATCGAGCCTGGCCTTGAGGGTCCACAC ATCCCTGCTCCCCCTGCCTCAGACATCTACGCGGCGAAATCGAGCCTGGCCTTGAGGGTCCACAC T C PLAAT3 Ensembl:ENSG00000176485 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63614008..63614108 26863196 MeRIP-seq:(Medium) rs760182104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1251547,Human_Splice_Rec_1251560,Human_Splice_Rec_1251561,Human_Splice_Rec_1251567 56554 RMVar_ID_56554 Human_SNP_ID_469525018 m1A Human chr11 - 63614306 63614306 63614306 GGTGCCTGGGATGCTTCTCCCCTTCCGCGAGGAAGAGATCTAATTGGGTAGGGCGGGTGTAGACT GGTGCCTGGGATGCTTCTCCCCTTCCGCGAGGCAGAGATCTAATTGGGTAGGGCGGGTGTAGACT T G PLAAT3 Ensembl:ENSG00000176485 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:63614176..63614425 26863196 MeRIP-seq:(Medium) rs1232112668 Functional Loss SNV dbSNP153 33..33 33 - - - 56555 RMVar_ID_56555 Human_SNP_ID_469533842 m1A Human chr11 + 63647030 63647030 63647030 CACGGGGCACACCGCTGCCTTAGGACCTTCGTACTGGCTCCTCCCACTAACTATAAGTTCTTCTC CACGGGGCACACCGCTGCCTTAGGACCTTCGTTCTGGCTCCTCCCACTAACTATAAGTTCTTCTC A T AP000753.2 Ensembl:ENSG00000256789 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63646979..63647065 26863196 MeRIP-seq:(Medium) rs1285195570 Functional Loss SNV dbSNP153 33..33 33 - - - 56556 RMVar_ID_56556 Human_SNP_ID_469536802 m1A Human chr11 - 63658869 63658869 63658869 GAAAGTGGCCATTCAAATTGGTTGGGTGACCCAGAAGAACCGTTAACAGGATTTTCCTGGAGAGG GAAAGTGGCCATTCAAATTGGTTGGGTGACCCGGAAGAACCGTTAACAGGATTTTCCTGGAGAGG T C ATL3 Ensembl:ENSG00000184743 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:63658820..63658915 32194978 MeRIP-seq:(Medium) rs771575716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22435403,Human_RBP_ID_23511669 Human_Splice_Rec_1251584,Human_Splice_Rec_1251608,Human_Splice_Rec_1251634 RMVar_hsa_circ_359466,RMVar_hsa_circ_344857,RMVar_hsa_circ_150358,RMVar_hsa_circ_150362,RMVar_hsa_circ_150359,RMVar_hsa_circ_343670,RMVar_hsa_circ_100822,RMVar_hsa_circ_286440,RMVar_hsa_circ_150361 56557 RMVar_ID_56557 Human_SNP_ID_469540209 m1A Human chr11 + 63671373 63671361 63671374 CTCCGCCTTCAAAGCAGAAGCAGCAGGGGTGCAGAGGAGAGGGACGGGTGCGGGCGGGAACGAAC CTCCGCCTTCAAAGCAGAAGC_____________AGGAGAGGGACGGGTGCGGGCGGGAACGAAC CAGCAGGGGTGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63671326..63671552 26863196 MeRIP-seq:(Medium) rs1355094138 Functional Loss DEL dbSNP153 22..34 33 - - - 56558 RMVar_ID_56558 Human_SNP_ID_469540224 m1A Human chr11 + 63671378 63671378 63671378 CCTTCAAAGCAGAAGCAGCAGGGGTGCAGAGGAGAGGGACGGGTGCGGGCGGGAACGAACCGGGC CCTTCAAAGCAGAAGCAGCAGGGGTGCAGAGGGGAGGGACGGGTGCGGGCGGGAACGAACCGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63671318..63671545 26863196 MeRIP-seq:(Medium) rs984991529 Functional Loss SNV dbSNP153 33..33 33 - - - 56559 RMVar_ID_56559 Human_SNP_ID_469540305 m1A Human chr11 + 63671521 63671521 63671521 GCGAGCGCAGCGCGGTCTGCGTGGCCCAACGGACAGCCCGAGGCGTGGCGAGCGCAGGACGAGGC GCGAGCGCAGCGCGGTCTGCGTGGCCCAACGGTCAGCCCGAGGCGTGGCGAGCGCAGGACGAGGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:63671351..63671600 26863196 MeRIP-seq:(Medium) rs990971782 Functional Loss SNV dbSNP153 33..33 33 - - - 56560 RMVar_ID_56560 Human_SNP_ID_469543065 m1A Human chr11 - 63681649 63681649 63681649 CGAGGAGATGGAATGGGACTGAGTGGCCGCCGACGGCTCCGCCATGGCTACGCGAGCGAGGGTGG CGAGGAGATGGAATGGGACTGAGTGGCCGCCGGCGGCTCCGCCATGGCTACGCGAGCGAGGGTGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:63681501..63681753;chr11:63681501..63681718;chr11:63681501..63681701 26863196 MeRIP-seq:(Medium) rs750626740 Functional Loss SNV dbSNP153 33..33 33 - - - 56561 RMVar_ID_56561 Human_SNP_ID_469564838 m1A Human chr11 - 63762146 63762142 63762147 GAAGGAGGAGCGAGGGCAGAGGCGGGGACGGGAGGACCCCAACTAGCTGTGCTGATGTTAATCCC GAAGGAGGAGCGAGGGCAGAGGCGGGGACGG_____CCCCAACTAGCTGTGCTGATGTTAATCCC GTCCTC G C11orf95 Ensembl:ENSG00000188070 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63761873..63762210 26863196 MeRIP-seq:(Medium) rs1311543988 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_749415,Human_RBP_ID_9322099 Human_miRNA_ID_1967258 RMVar_hsa_circ_99504,RMVar_hsa_circ_150369 56562 RMVar_ID_56562 Human_SNP_ID_469565302 m1A Human chr11 + 63763397 63763397 63763397 GGGGCGGGGCCGATCCGACCCGACCCGACCTGACCCGGGGGCCCGCTAGGCCGCTACGCCCGACA GGGGCGGGGCCGATCCGACCCGACCCGACCTGGCCCGGGGGCCCGCTAGGCCGCTACGCCCGACA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:63763139..63763440 26863410 MeRIP-seq:(Medium) rs1271340244 Functional Loss SNV dbSNP153 33..33 33 - - - 56563 RMVar_ID_56563 Human_SNP_ID_469565303 m1A Human chr11 + 63763397 63763397 63763397 GGGGCGGGGCCGATCCGACCCGACCCGACCTGACCCGGGGGCCCGCTAGGCCGCTACGCCCGACA GGGGCGGGGCCGATCCGACCCGACCCGACCTGTCCCGGGGGCCCGCTAGGCCGCTACGCCCGACA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:63763139..63763440 26863410 MeRIP-seq:(Medium) rs1271340244 Functional Loss SNV dbSNP153 33..33 33 - - - 56564 RMVar_ID_56564 Human_SNP_ID_469565568 m1A Human chr11 + 63763967 63763967 63763967 CTCCAGTCACCCCATCTTTGCCCTTCTATCCCATCCTCCAGTCCCTTCTGCCCCAGCAACTGCCC CTCCAGTCACCCCATCTTTGCCCTTCTATCCCGTCCTCCAGTCCCTTCTGCCCCAGCAACTGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63763789..63764093 26863196 MeRIP-seq:(Medium) rs1384643614 Functional Loss SNV dbSNP153 33..33 33 - - - 56565 RMVar_ID_56565 Human_SNP_ID_469565599 m1A Human chr11 + 63764041 63764041 63764041 TCTCCGCCTGCTCTGGCCCCACCGCTCACCCCACTCCTCCTCCTCCTCCTCTGGCTCCTCCTCCT TCTCCGCCTGCTCTGGCCCCACCGCTCACCCCCCTCCTCCTCCTCCTCCTCTGGCTCCTCCTCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63763461..63766331 26863196 MeRIP-seq:(Medium) rs1317186828 Functional Loss SNV dbSNP153 33..33 33 - - - 56566 RMVar_ID_56566 Human_SNP_ID_469566012 m1A Human chr11 - 63765065 63765065 63765065 GAACTGGTTCCGGGCCGAGTGTCTCATGGACTATGACCCGCGGGGGAACCGGCTGGTGTGCATGG GAACTGGTTCCGGGCCGAGTGTCTCATGGACTGTGACCCGCGGGGGAACCGGCTGGTGTGCATGG T C C11orf95 Ensembl:ENSG00000188070 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63765026..63765227 26863196 MeRIP-seq:(Medium) rs769007592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5489972 Human_Splice_Rec_1251761 Human_miRNA_ID_3002672 RMVar_hsa_circ_99504,RMVar_hsa_circ_150369 56567 RMVar_ID_56567 Human_SNP_ID_469566758 m1A Human chr11 + 63767547 63767547 63767547 TGGTCTCTAAGCATCCTTCCAGCGCTGGATCCAGGCTAGTCTAAGGTGGATTGGCCCTTTAAGAG TGGTCTCTAAGCATCCTTCCAGCGCTGGATCCGGGCTAGTCTAAGGTGGATTGGCCCTTTAAGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63767545..63768760 26863196 MeRIP-seq:(Medium) rs1049746533 Functional Loss SNV dbSNP153 33..33 33 - - - 56568 RMVar_ID_56568 Human_SNP_ID_469567277 m1A Human chr11 + 63768914 63768914 63768914 TCGCGGGGGGCTGGGGGGAAAGGCGGGAGGCAACGAGCCCAGCCGAGGCTCAGCAGCCTGCGCCC TCGCGGGGGGCTGGGGGGAAAGGCGGGAGGCACCGAGCCCAGCCGAGGCTCAGCAGCCTGCGCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63768873..63768956 26863196 MeRIP-seq:(Medium) rs1446534139 Functional Loss SNV dbSNP153 33..33 33 - - - 56569 RMVar_ID_56569 Human_SNP_ID_469567322 m1A Human chr11 - 63769075 63769072 63769075 GGGGGCGGTGGCCGCGAGCCGAGCCCGGGTGGAAGCGCGTCGCAGCGGACGCGGGCGCCCCTCGC GGGGGCGGTGGCCGCGAGCCGAGCCCGGGTGG___CGCGTCGCAGCGGACGCGGGCGCCCCTCGC GCTT G lnc-C11orf95-1,lnc-C11orf95-1:2,lnc-C11orf95-1:3,lnc-C11orf95-1:4 RNACentral:URS0000D6EC19,RNACentral:URS0000D6D92B,RNACentral:URS0000D6E9AA,RNACentral:URS0000D6E97F lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63769025..63769190 26863196 MeRIP-seq:(Medium) rs1352133204 Functional Loss DEL dbSNP153 33..35 33 - - - 56570 RMVar_ID_56570 Human_SNP_ID_469578568 m1A Human chr11 + 63813485 63813485 63813485 CCCGGATTGAGCCCTCCCCGCCCGGGCTCCCGACGCGCCGAGGTCTCGGGGAGGCCCGGACGCGC CCCGGATTGAGCCCTCCCCGCCCGGGCTCCCGGCGCGCCGAGGTCTCGGGGAGGCCCGGACGCGC A G SPINDOC Ensembl:ENSG00000168005 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63813437..63813550 26863196 MeRIP-seq:(Medium) rs1369300465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184144,Human_RBP_ID_18416837 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371 56571 RMVar_ID_56571 Human_SNP_ID_469578711 m1A Human chr11 + 63813804 63813804 63813804 TGGTGGTGGCCGTAATTCCGCGGCCCGAGCCGATGCTCAGAGGTGAGGATGGAGGGGATTCCACT TGGTGGTGGCCGTAATTCCGCGGCCCGAGCCGCTGCTCAGAGGTGAGGATGGAGGGGATTCCACT A C SPINDOC Ensembl:ENSG00000168005 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:63813441..63817871;chr11:63813601..63813846 26863196 MeRIP-seq:(Medium) rs1191351397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19051911 Human_Splice_Rec_1251767 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371 56572 RMVar_ID_56572 Human_SNP_ID_469580167 m1A Human chr11 - 63818750 63818749 63818750 GGAACTGTGAGTGAAAAAGCCTCAGGAGCTGCAGGCGCCCTGCGCCCAGGCCCTGCTCCATCCTC GGAACTGTGAGTGAAAAAGCCTCAGGAGCTGC_GGCGCCCTGCGCCCAGGCCCTGCTCCATCCTC CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:63818746..63818925 26863196 MeRIP-seq:(Medium) rs1052867312 Functional Loss DEL dbSNP153 33..33 33 - - - 56573 RMVar_ID_56573 Human_SNP_ID_469580230 m1A Human chr11 + 63818910 63818908 63818910 CCCCGCCGGCTTCGTCTTGCAGCTCTTCTCCCACACCCAGCTCAGGGGCCCAGACAGCAAGGACT CCCCGCCGGCTTCGTCTTGCAGCTCTTCTCC__CACCCAGCTCAGGGGCCCAGACAGCAAGGACT CCA C SPINDOC Ensembl:ENSG00000168005 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:63818786..63818950 26863196 MeRIP-seq:(Medium) rs769035932 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_226961,Human_RBP_ID_5110807,Human_RBP_ID_17232680,Human_RBP_ID_18973894,Human_RBP_ID_27413443 Human_Splice_Rec_1251775,Human_Splice_Rec_1251779,Human_Splice_Rec_1251783 Human_miRNA_ID_1003725,Human_miRNA_ID_1355922,Human_miRNA_ID_1973173,Human_miRNA_ID_1975350,Human_miRNA_ID_2295583,Human_miRNA_ID_2613154 RMVar_hsa_circ_45965,RMVar_hsa_circ_78377,RMVar_hsa_circ_316290,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150373,RMVar_hsa_circ_150372,RMVar_hsa_circ_325284,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809,RMVar_hsa_circ_371293,RMVar_hsa_circ_150377 56574 RMVar_ID_56574 Human_SNP_ID_469582514 m1A Human chr11 + 63827033 63827033 63827033 CAGCCTCCTGCAAGACTGGTCCAGGCACCCCCAGGGCACCAAGCGTGTGGGAGCAGGTGACACCT CAGCCTCCTGCAAGACTGGTCCAGGCACCCCCTGGGCACCAAGCGTGTGGGAGCAGGTGACACCT A T SPINDOC Ensembl:ENSG00000168005 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63826984..63827053 26863196 MeRIP-seq:(Medium) rs373324696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809,RMVar_hsa_circ_81189,RMVar_hsa_circ_150379 56575 RMVar_ID_56575 Human_SNP_ID_469582681 m1A Human chr11 - 63827527 63827527 63827527 CCTGAACAAGTGGGGAGGAGAGGTGTCCCCCGAGGTAGTGGGACTCAGTTCAAACCCCCTTATGA CCTGAACAAGTGGGGAGGAGAGGTGTCCCCCGGGGTAGTGGGACTCAGTTCAAACCCCCTTATGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63827478..63827639 26863196 MeRIP-seq:(Medium) rs1056035226 Functional Loss SNV dbSNP153 33..33 33 - - - 56576 RMVar_ID_56576 Human_SNP_ID_469602419 m1A Human chr11 + 63904835 63904835 63904835 TCCCTGTTGCCTCCCCATCCGCCCACAACATCAGCAGCAGTGGTGGAGCCCCAGACCGAACTAAC TCCCTGTTGCCTCCCCATCCGCCCACAACATCGGCAGCAGTGGTGGAGCCCCAGACCGAACTAAC A G MARK2 Ensembl:ENSG00000072518 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63904734..63904886 26863196 MeRIP-seq:(Medium) rs749697940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26320035 Human_Splice_Rec_1251876,Human_Splice_Rec_1251908,Human_Splice_Rec_1251940,Human_Splice_Rec_1252096 RMVar_hsa_circ_90714,RMVar_hsa_circ_150380,RMVar_hsa_circ_320831,RMVar_hsa_circ_150384,RMVar_hsa_circ_96351,RMVar_hsa_circ_103218,RMVar_hsa_circ_150388 56577 RMVar_ID_56577 Human_SNP_ID_469604627 m1A Human chr11 + 63911968 63911968 63911968 CGCTGTGGCGGGGGGCAGCCAGAGCGGGGCGGATGAGAGGCGGTGGGGGCTGGTTGGGGGCCAGC CGCTGTGGCGGGGGGCAGCCAGAGCGGGGCGGGTGAGAGGCGGTGGGGGCTGGTTGGGGGCCAGC A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63911925..63912173 26863196 MeRIP-seq:(Medium) rs1427201653 Functional Loss SNV dbSNP153 33..33 33 - - - 56578 RMVar_ID_56578 Human_SNP_ID_469606512 m1A Human chr11 + 63916999 63916999 63916999 CCGGCGGCGGCGGCGGCGGCGACGGCGGCGGGACGGCGCGCACGGCGCGCGGCGCTGGGCAGAGT CCGGCGGCGGCGGCGGCGGCGACGGCGGCGGGTCGGCGCGCACGGCGCGCGGCGCTGGGCAGAGT A T RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63916992..63917137 26863196 MeRIP-seq:(Medium) rs1235422949 Functional Loss SNV dbSNP153 33..33 33 - - - 56579 RMVar_ID_56579 Human_SNP_ID_469606522 m1A Human chr11 - 63917022 63917022 63917022 TGCGCTCCGCCCGCCTCCCGGCAACTCTGCCCAGCGCCGCGCGCCGTGCGCGCCGTCCCGCCGCC TGCGCTCCGCCCGCCTCCCGGCAACTCTGCCCGGCGCCGCGCGCCGTGCGCGCCGTCCCGCCGCC T C RCOR2 Ensembl:ENSG00000167771 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63916973..63917092 26863196 MeRIP-seq:(Medium) rs1446971390 Functional Loss SNV dbSNP153 33..33 33 - - - 56580 RMVar_ID_56580 Human_SNP_ID_469606558 m1A Human chr11 - 63917132 63917132 63917132 ATTGTGTGCGCGAGGAGCGAGCGGCGGCGGAGAGCGGGCGAGCAAGCGGCATCCCGAGCGCGGCG ATTGTGTGCGCGAGGAGCGAGCGGCGGCGGAGGGCGGGCGAGCAAGCGGCATCCCGAGCGCGGCG T C RCOR2 Ensembl:ENSG00000167771 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63916821..63917168 26863196 MeRIP-seq:(Medium) rs1199468130 Functional Loss SNV dbSNP153 33..33 33 - - - 56581 RMVar_ID_56581 Human_SNP_ID_469612402 m1A Human chr11 - 63939051 63939049 63939051 ACGCTCAGCTTCTTCTTCACACACTTGCCGGCAGGGAGGCGGCAACGGCGGTGGCTGCAACAGCG ACGCTCAGCTTCTTCTTCACACACTTGCCGGC__GGAGGCGGCAACGGCGGTGGCTGCAACAGCG CCT C lnc-RCOR2-2 RNACentral:URS00008BB997 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63939001..63939139 26863196 MeRIP-seq:(Medium) rs1565168067 Functional Loss DEL dbSNP153 33..34 33 - - - 56582 RMVar_ID_56582 Human_SNP_ID_469612411 m1A Human chr11 + 63939067 63939065 63939068 GCCGTTGCCGCCTCCCTGCCGGCAAGTGTGTGAAGAAGAAGCTGAGCGTTGTCGCCGCCGCTATG GCCGTTGCCGCCTCCCTGCCGGCAAGTGTGT___GAAGAAGCTGAGCGTTGTCGCCGCCGCTATG TGAA T NAA40 Ensembl:ENSG00000110583 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63939016..63939156 26863196 MeRIP-seq:(Medium) rs746521848 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_807339,Human_RBP_ID_4168329,Human_RBP_ID_5549560,Human_RBP_ID_9362401,Human_RBP_ID_18416573,Human_RBP_ID_24542655 Human_Splice_Rec_1252159,Human_Splice_Rec_1252171,Human_Splice_Rec_1252179,Human_Splice_Rec_1252191,Human_Splice_Rec_1252199,Human_Splice_Rec_1252207 Human_miRNA_ID_2539859,Human_miRNA_ID_2909255 RMVar_hsa_circ_83810,RMVar_hsa_circ_150390 56583 RMVar_ID_56583 Human_SNP_ID_469612413 m1A Human chr11 + 63939070 63939070 63939070 GTTGCCGCCTCCCTGCCGGCAAGTGTGTGAAGAAGAAGCTGAGCGTTGTCGCCGCCGCTATGGGG GTTGCCGCCTCCCTGCCGGCAAGTGTGTGAAGGAGAAGCTGAGCGTTGTCGCCGCCGCTATGGGG A G NAA40 Ensembl:ENSG00000110583 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63939019..63939145 26863196 MeRIP-seq:(Medium) rs1565168097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807339,Human_RBP_ID_4185001,Human_RBP_ID_9362401,Human_RBP_ID_18416573,Human_RBP_ID_24542655 Human_Splice_Rec_1252159,Human_Splice_Rec_1252171,Human_Splice_Rec_1252179,Human_Splice_Rec_1252191,Human_Splice_Rec_1252199,Human_Splice_Rec_1252207 Human_miRNA_ID_2909255 RMVar_hsa_circ_83810,RMVar_hsa_circ_150390 56584 RMVar_ID_56584 Human_SNP_ID_469614123 m1A Human chr11 - 63945796 63945796 63945796 AAAAGCAACGTTAGCTGGAATGGCTGTGGCCAATCAAGCACTGACTTTCCCTTTAAGGAATCGAA AAAAGCAACGTTAGCTGGAATGGCTGTGGCCAGTCAAGCACTGACTTTCCCTTTAAGGAATCGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63945793..63945925 26863196 MeRIP-seq:(Medium) rs761105960 Functional Loss SNV dbSNP153 33..33 33 - - - 56585 RMVar_ID_56585 Human_SNP_ID_469617190 m1A Human chr11 + 63956879 63956879 63956879 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGACTCGCTTGAACCCAGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGACTCGCTTGAACCCAGGAGGTGGAGGTT A G NAA40 Ensembl:ENSG00000110583 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1402498532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399642 56586 RMVar_ID_56586 Human_SNP_ID_469622262 m1A Human chr11 - 63974736 63974736 63974736 GCAACGAATGGATCTTGGCGCGCGGCACTGGGAGCCGCCGGGCCGAGCCTGTCAAGCCCCGCAGC GCAACGAATGGATCTTGGCGCGCGGCACTGGGGGCCGCCGGGCCGAGCCTGTCAAGCCCCGCAGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:63974601..63986152 26863410 MeRIP-seq:(Medium) rs1437255886 Functional Loss SNV dbSNP153 33..33 33 - - - 56587 RMVar_ID_56587 Human_SNP_ID_469622669 m1A Human chr11 - 63976177 63976177 63976177 GAAAGAAGGCACCTCGGAGTCAGTATTCCCCTAGGCTCTCTAAGTCCTTGCAGTTCCCAGGCAGC GAAAGAAGGCACCTCGGAGTCAGTATTCCCCTGGGCTCTCTAAGTCCTTGCAGTTCCCAGGCAGC T C lnc-MACROD1-5 RNACentral:URS0000D594F2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63976174..63976418 26863196 MeRIP-seq:(Medium) rs778077401 Functional Loss SNV dbSNP153 33..33 33 - - - 56588 RMVar_ID_56588 Human_SNP_ID_469622712 m1A Human chr11 + 63976300 63976300 63976300 TGCCAGCGGGCTGGATCCTGTCACACCTGGAGACCTACAGGAGGCCAGAGTGAAGGGGTCCGTTC TGCCAGCGGGCTGGATCCTGTCACACCTGGAGCCCTACAGGAGGCCAGAGTGAAGGGGTCCGTTC A C COX8A,AP000721.1 Ensembl:ENSG00000176340,Ensembl:ENSG00000256100 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63976251..63976525 26863196 MeRIP-seq:(Medium) rs1288652329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399668,Human_RBP_ID_1458571,Human_RBP_ID_1780871,Human_RBP_ID_4168404,Human_RBP_ID_8354602,Human_RBP_ID_9004820,Human_RBP_ID_9322103,Human_RBP_ID_11665632,Human_RBP_ID_17466978,Human_RBP_ID_17648445,Human_RBP_ID_17798566,Human_RBP_ID_18188246,Human_RBP_ID_22433056,Human_RBP_ID_22491498,Human_RBP_ID_23207338,Human_RBP_ID_26893413,Human_RBP_ID_27203925 Human_Splice_Rec_1252248 Human_miRNA_ID_2784094 RMVar_hsa_circ_117684,RMVar_hsa_circ_81932,RMVar_hsa_circ_150392,RMVar_hsa_circ_150393 56589 RMVar_ID_56589 Human_SNP_ID_469628557 m1A Human chr11 - 63997150 63997150 63997150 CGCGCTGCAGGTAGCCCGAGGTGAGCAGCCGCAGGTAGACCACAAGGTAGTCGGAGGTGCTCTGG CGCGCTGCAGGTAGCCCGAGGTGAGCAGCCGCGGGTAGACCACAAGGTAGTCGGAGGTGCTCTGG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63997104..63997196 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 56590 RMVar_ID_56590 Human_SNP_ID_469628672 m1A Human chr11 - 63997480 63997480 63997480 TAGAGAAGGTAGACCTTGGGCTCGGAGCCCTCAGGGAAGATGTGCGGATTGGTGGTGCCGCCCTC TAGAGAAGGTAGACCTTGGGCTCGGAGCCCTCCGGGAAGATGTGCGGATTGGTGGTGCCGCCCTC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:63997326..63998324 32194978 MeRIP-seq:(Medium) rs1245730408 Functional Loss SNV dbSNP153 33..33 33 - - - 56591 RMVar_ID_56591 Human_SNP_ID_469628701 m1A Human chr11 - 63997572 63997561 63997572 TACATGTCTAGCGCCTGGCAGAGGGGGGCAGCAGGGCAGCAGCGGGCTGGAGCCAGCCCTATTTG TACATGTCTAGCGCCTGGCAGAGGGGGGCAGC___________GGGCTGGAGCCAGCCCTATTTG CGCTGCTGCCCT C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63997522..63997690 26863196 MeRIP-seq:(Medium) rs760868231 Functional Loss DEL dbSNP153 33..43 33 - - - 56592 RMVar_ID_56592 Human_SNP_ID_469628710 m1A Human chr11 - 63997572 63997572 63997572 TACATGTCTAGCGCCTGGCAGAGGGGGGCAGCAGGGCAGCAGCGGGCTGGAGCCAGCCCTATTTG TACATGTCTAGCGCCTGGCAGAGGGGGGCAGCGGGGCAGCAGCGGGCTGGAGCCAGCCCTATTTG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63997522..63997690 26863196 MeRIP-seq:(Medium) rs769977704 Functional Loss SNV dbSNP153 33..33 33 - - - 56593 RMVar_ID_56593 Human_SNP_ID_469628764 m1A Human chr11 + 63997683 63997683 63997683 TCCTGTCACATGACCCCCCCCCATGTTTTATTAAAGGGGGTGCTGGTGGTGAGCCGTGTGTGCGT TCCTGTCACATGACCCCCCCCCATGTTTTATTTAAGGGGGTGCTGGTGGTGAGCCGTGTGTGCGT A T OTUB1 Ensembl:ENSG00000167770 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:63997633..63997762 26863196 MeRIP-seq:(Medium) rs1440699823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32528,Human_RBP_ID_399697,Human_RBP_ID_987788,Human_RBP_ID_5111127,Human_RBP_ID_6084029,Human_RBP_ID_17798579,Human_RBP_ID_18176154,Human_RBP_ID_18933606,Human_RBP_ID_19654749,Human_RBP_ID_21883557,Human_RBP_ID_23512090,Human_RBP_ID_24403491,Human_RBP_ID_26893437,Human_RBP_ID_27203941,Human_RBP_ID_27413528 Human_Splice_Rec_1252293 56594 RMVar_ID_56594 Human_SNP_ID_469628932 m1A Human chr11 + 63998143 63998143 63998143 CTGGGCCTCCCACAGGGTGCCCGGGCAGTGCCATCCTGGTGGGGGAGGGCAGCCTTCAAACGTGT CTGGGCCTCCCACAGGGTGCCCGGGCAGTGCCGTCCTGGTGGGGGAGGGCAGCCTTCAAACGTGT A G OTUB1 Ensembl:ENSG00000167770 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63998093..63998300 26863196 MeRIP-seq:(Medium) rs377502278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399709,Human_RBP_ID_1162598,Human_RBP_ID_17798587,Human_RBP_ID_21966094 56595 RMVar_ID_56595 Human_SNP_ID_469628967 m1A Human chr11 + 63998262 63998262 63998262 CGCCCCAGGCCCCCTGCCTGTGCCTGCCTTGCACCCCCTCTGCTTGGGCCACGGTGTCTCTGCAT CGCCCCAGGCCCCCTGCCTGTGCCTGCCTTGCGCCCCCTCTGCTTGGGCCACGGTGTCTCTGCAT A G OTUB1 Ensembl:ENSG00000167770 Protein coding exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr11:63998251..63998350;chr11:63998162..63998329 26863196 MeRIP-seq:(Medium) rs912763343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32529,Human_RBP_ID_399712,Human_RBP_ID_751507,Human_RBP_ID_18932484,Human_RBP_ID_23512097 Human_miRNA_ID_515596,Human_miRNA_ID_519821 56596 RMVar_ID_56596 Human_SNP_ID_469628971 m1A Human chr11 - 63998268 63998267 63998268 CAGGCAATGCAGAGACACCGTGGCCCAAGCAGAGGGGGTGCAAGGCAGGCACAGGCAGGGGGCCT CAGGCAATGCAGAGACACCGTGGCCCAAGCAG_GGGGGTGCAAGGCAGGCACAGGCAGGGGGCCT CT C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63998103..63998302 26863196 MeRIP-seq:(Medium) rs972830363 Functional Loss DEL dbSNP153 33..33 33 - - - 56597 RMVar_ID_56597 Human_SNP_ID_469628983 m1A Human chr11 - 63998299 63998299 63998299 GCGGGGAAGAAAAGAGGTGAAGGCAAAAAGGCAGGCAATGCAGAGACACCGTGGCCCAAGCAGAG GCGGGGAAGAAAAGAGGTGAAGGCAAAAAGGCCGGCAATGCAGAGACACCGTGGCCCAAGCAGAG T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:63998195..63998350 26863196 MeRIP-seq:(Medium) rs760284878 Functional Loss SNV dbSNP153 33..33 33 - - - 56598 RMVar_ID_56598 Human_SNP_ID_469629116 m1A Human chr11 + 63998680 63998667 63998681 GCGACCTCTCAGAGCTGGGAGCGGGGTCCCGAAGGCGGGTCTGAGGGCAGAGCAGAGTCAGAGGT GCGACCTCTCAGAGCTGGGA______________GCGGGTCTGAGGGCAGAGCAGAGTCAGAGGT AGCGGGGTCCCGAAG A OTUB1 Ensembl:ENSG00000167770 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63998576..63999030 26863196 MeRIP-seq:(Medium) rs1278368384 Functional Loss DEL dbSNP153 21..34 33 - - - 56599 RMVar_ID_56599 Human_SNP_ID_469629125 m1A Human chr11 + 63998680 63998680 63998680 GCGACCTCTCAGAGCTGGGAGCGGGGTCCCGAAGGCGGGTCTGAGGGCAGAGCAGAGTCAGAGGT GCGACCTCTCAGAGCTGGGAGCGGGGTCCCGAGGGCGGGTCTGAGGGCAGAGCAGAGTCAGAGGT A G OTUB1 Ensembl:ENSG00000167770 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63998576..63999030 26863196 MeRIP-seq:(Medium) rs1450735814 Functional Loss SNV dbSNP153 33..33 33 - - - 56600 RMVar_ID_56600 Human_SNP_ID_469629455 m1A Human chr11 + 63999371 63999371 63999371 TGTGCTGCTCCAGCCACTCTCGCAGCGTGGCCAGCACGATCTCGGCGGCCGCCTCACAGGGGTAG TGTGCTGCTCCAGCCACTCTCGCAGCGTGGCCGGCACGATCTCGGCGGCCGCCTCACAGGGGTAG A G OTUB1 Ensembl:ENSG00000167770 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63999235..63999442 26863196 MeRIP-seq:(Medium) rs370776611 Functional Loss SNV dbSNP153 33..33 33 - - - 56601 RMVar_ID_56601 Human_SNP_ID_469632422 m1A Human chr11 - 64010138 64010114 64010138 ACACCCCAGGCAACACTTCAACCAACACCCCAACCAACCCCCCAACCAACACCCCAGCCAACCCC ACACCCCAGGCAACACTTCAACCAACACCCCA________________________GCCAACCCC CTGGGGTGTTGGTTGGGGGGTTGGT C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64010128..64010249 26863196 MeRIP-seq:(Medium) rs1565192927 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_193366 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_150397 56602 RMVar_ID_56602 Human_SNP_ID_469632439 m1A Human chr11 - 64010138 64010138 64010138 ACACCCCAGGCAACACTTCAACCAACACCCCAACCAACCCCCCAACCAACACCCCAGCCAACCCC ACACCCCAGGCAACACTTCAACCAACACCCCAGCCAACCCCCCAACCAACACCCCAGCCAACCCC T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64010128..64010249 26863196 MeRIP-seq:(Medium) rs867110388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193366 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_150397 56603 RMVar_ID_56603 Human_SNP_ID_469632581 m1A Human chr11 - 64010383 64010383 64010383 AACACTCCAGCCAACACCCCGGTCAACACCCCAGCCAACATCCCAGCCAACACTCCAACCAACAC AACACTCCAGCCAACACCCCGGTCAACACCCCGGCCAACATCCCAGCCAACACTCCAACCAACAC T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64010322..64010406 26863196 MeRIP-seq:(Medium) rs144964298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_192981,Human_RBP_ID_24529529,Human_RBP_ID_26754780,Human_RBP_ID_26803684 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_150397 56604 RMVar_ID_56604 Human_SNP_ID_469633856 m1A Human chr11 + 64015132 64015132 64015132 TCTCCAGCTCTGGGGAAGGGAGGCACCCTGTGAGGACAGTGGGGAAGGTGGATTGCAGTGAGATG TCTCCAGCTCTGGGGAAGGGAGGCACCCTGTGGGGACAGTGGGGAAGGTGGATTGCAGTGAGATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64015127..64015259 26863196 MeRIP-seq:(Medium) rs1298154362 Functional Loss SNV dbSNP153 33..33 33 - - - 56605 RMVar_ID_56605 Human_SNP_ID_469633960 m1A Human chr11 + 64015416 64015416 64015416 TAGGTCTTCAGACTTGGGCACAGGGTCTTCCCAGTCCTCCGGGGCGGTAGTAGACGATGGTGAAG TAGGTCTTCAGACTTGGGCACAGGGTCTTCCCTGTCCTCCGGGGCGGTAGTAGACGATGGTGAAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64015412..64015519 26863196 MeRIP-seq:(Medium) rs1345518798 Functional Loss SNV dbSNP153 33..33 33 - - - 56606 RMVar_ID_56606 Human_SNP_ID_469635716 m1A Human chr11 - 64021952 64021946 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCAC______CCCCCCCCCCCCCGGCCCCCTGCCACT GGGGGGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1451509405 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56607 RMVar_ID_56607 Human_SNP_ID_469635717 m1A Human chr11 - 64021952 64021947 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCAC_____CCCCCCCCCCCCCCGGCCCCCTGCCACT GGGGGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1328336553 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56608 RMVar_ID_56608 Human_SNP_ID_469635720 m1A Human chr11 - 64021952 64021948 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCAC____CCCCCCCCCCCCCCCGGCCCCCTGCCACT GGGGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1258169312 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56609 RMVar_ID_56609 Human_SNP_ID_469635722 m1A Human chr11 - 64021952 64021949 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCAC___CCCCCCCCCCCCCCCCGGCCCCCTGCCACT GGGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1230185000 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56610 RMVar_ID_56610 Human_SNP_ID_469635723 m1A Human chr11 - 64021954 64021949 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTC_____CCCCCCCCCCCCCCCCGGCCCCCTGCCA GGGTGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1336994134 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56611 RMVar_ID_56611 Human_SNP_ID_469635728 m1A Human chr11 - 64021954 64021950 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTC____CCCCCCCCCCCCCCCCCGGCCCCCTGCCA GGTGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1268826541 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56612 RMVar_ID_56612 Human_SNP_ID_469635729 m1A Human chr11 - 64021954 64021950 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTC__ACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA GGTGT GGT MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1268826541 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56613 RMVar_ID_56613 Human_SNP_ID_469635730 m1A Human chr11 - 64021954 64021951 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTC___CCCCCCCCCCCCCCCCCCGGCCCCCTGCCA GTGT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1315344426 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56614 RMVar_ID_56614 Human_SNP_ID_469635731 m1A Human chr11 - 64021952 64021951 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCAC_CCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT GT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1341650734 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56615 RMVar_ID_56615 Human_SNP_ID_469635735 m1A Human chr11 - 64021952 64021952 64021952 CCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT CCCTCCAGATCCACTGCCCGCCGCCACCTCACCCCCCCCCCCCCCCCCCCCGGCCCCCTGCCACT T G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1193464642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56616 RMVar_ID_56616 Human_SNP_ID_469635740 m1A Human chr11 - 64021954 64021953 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTC_CACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA GT G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1565197683 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56617 RMVar_ID_56617 Human_SNP_ID_469635744 m1A Human chr11 - 64021954 64021954 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTCTCACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA T A MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1426059018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56618 RMVar_ID_56618 Human_SNP_ID_469635745 m1A Human chr11 - 64021954 64021954 64021954 ACCCCTCCAGATCCACTGCCCGCCGCCACCTCACACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA ACCCCTCCAGATCCACTGCCCGCCGCCACCTCCCACCCCCCCCCCCCCCCCCCGGCCCCCTGCCA T G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64021926..64021975 26863196 MeRIP-seq:(Medium) rs1426059018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56619 RMVar_ID_56619 Human_SNP_ID_469639278 m1A Human chr11 - 64035746 64035746 64035746 GCGGGGGCCGTGCGTGCAGGCGCGGAGCGGGGAGGGAGAGGAGGAGGAGGGGAGGGGGAGGAGGA GCGGGGGCCGTGCGTGCAGGCGCGGAGCGGGGGGGGAGAGGAGGAGGAGGGGAGGGGGAGGAGGA T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64035744..64036085 26863196 MeRIP-seq:(Medium) rs1190612693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56620 RMVar_ID_56620 Human_SNP_ID_469639279 m1A Human chr11 - 64035746 64035746 64035746 GCGGGGGCCGTGCGTGCAGGCGCGGAGCGGGGAGGGAGAGGAGGAGGAGGGGAGGGGGAGGAGGA GCGGGGGCCGTGCGTGCAGGCGCGGAGCGGGGCGGGAGAGGAGGAGGAGGGGAGGGGGAGGAGGA T G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64035744..64036085 26863196 MeRIP-seq:(Medium) rs1190612693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56621 RMVar_ID_56621 Human_SNP_ID_469639906 m1A Human chr11 - 64037949 64037949 64037949 AGCCCTTGAGAATCCTCCAGTCCAGGAGCAGGACCACTAACAACATGCGTCAAATGCACTTACAA AGCCCTTGAGAATCCTCCAGTCCAGGAGCAGGGCCACTAACAACATGCGTCAAATGCACTTACAA T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64037947..64038047 32194978 MeRIP-seq:(Medium) rs1260403343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56622 RMVar_ID_56622 Human_SNP_ID_469651195 m1A Human chr11 + 64083646 64083646 64083646 AATAAGCATGTAAGTGAGTAATGAGAGGCCGCAGTGAGATGCCAACGCCGGGTCAGAGCTAGGAC AATAAGCATGTAAGTGAGTAATGAGAGGCCGCCGTGAGATGCCAACGCCGGGTCAGAGCTAGGAC A C AP006333.3,FLRT1 Ensembl:ENSG00000256481,Ensembl:ENSG00000256824 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64083644..64083881 26863196 MeRIP-seq:(Medium) rs1016088425 Functional Loss SNV dbSNP153 33..33 33 - - - 56623 RMVar_ID_56623 Human_SNP_ID_469651233 m1A Human chr11 - 64083761 64083761 64083761 TTGACCTTGGGAATTTGGGGCTGGGGCCCTTCAGGAGTCACCGAACCCCCATTCCACACACTAGC TTGACCTTGGGAATTTGGGGCTGGGGCCCTTCGGGAGTCACCGAACCCCCATTCCACACACTAGC T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:64083721..64083850 26863196 MeRIP-seq:(Medium) rs938358570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56624 RMVar_ID_56624 Human_SNP_ID_469661690 m1A Human chr11 - 64123553 64123553 64123553 GAGCCAAGCCAGGGCAGGTGCCCCCATCTTGCACCCCCAACCCCCCCACCCCACCCATCGAGGCC GAGCCAAGCCAGGGCAGGTGCCCCCATCTTGCCCCCCCAACCCCCCCACCCCACCCATCGAGGCC T G MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64123548..64123649 32194978 MeRIP-seq:(Medium) rs1240721825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56625 RMVar_ID_56625 Human_SNP_ID_469662467 m1A Human chr11 + 64126884 64126884 64126884 ACCTCCAGAATCAGCCGCCCAGGTGCAGCACTATCTCCTTTCTTTTTCTTGGAAGCCGTCTCAGG ACCTCCAGAATCAGCCGCCCAGGTGCAGCACTGTCTCCTTTCTTTTTCTTGGAAGCCGTCTCAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64126879..64127025 26863196 MeRIP-seq:(Medium) rs1194111062 Functional Loss SNV dbSNP153 33..33 33 - - - 56626 RMVar_ID_56626 Human_SNP_ID_469662468 m1A Human chr11 + 64126884 64126884 64126884 ACCTCCAGAATCAGCCGCCCAGGTGCAGCACTATCTCCTTTCTTTTTCTTGGAAGCCGTCTCAGG ACCTCCAGAATCAGCCGCCCAGGTGCAGCACTTTCTCCTTTCTTTTTCTTGGAAGCCGTCTCAGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64126879..64127025 26863196 MeRIP-seq:(Medium) rs1194111062 Functional Loss SNV dbSNP153 33..33 33 - - - 56627 RMVar_ID_56627 Human_SNP_ID_469666835 m1A Human chr11 - 64144023 64144021 64144024 GGAAAAATGGGGGCAGGGAGCATAAGATAATAAGGACAGGGAGACCCAGAGCTTGGGGTGGGAGG GGAAAAATGGGGGCAGGGAGCATAAGATAAT___GACAGGGAGACCCAGAGCTTGGGGTGGGAGG CCTT C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64144020..64144326 26863196 MeRIP-seq:(Medium) rs1472120808 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_259426,Human_RBP_ID_3384197,Human_RBP_ID_8064276,Human_RBP_ID_9322118,Human_RBP_ID_9414158,Human_RBP_ID_11666354,Human_RBP_ID_18932509,Human_RBP_ID_19695825,Human_RBP_ID_24362984,Human_RBP_ID_24550948 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 56628 RMVar_ID_56628 Human_SNP_ID_469667545 m1A Human chr11 + 64146740 64146738 64146740 TCCATCACCCACACCCCATGCATCACACAAGCACAGACACACACACATCACGCACACACACGCAT TCCATCACCCACACCCCATGCATCACACAAG__CAGACACACACACATCACGCACACACACGCAT GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64146738..64146938 26863196 MeRIP-seq:(Medium) rs754300993 Functional Loss DEL dbSNP153 32..33 33 - - - 56629 RMVar_ID_56629 Human_SNP_ID_469667571 m1A Human chr11 + 64146812 64146812 64146812 ATCATACAAATGCATACGCACACCCCACACACATAGGCCAAACTCCTGACCTCACACACACACTC ATCATACAAATGCATACGCACACCCCACACACGTAGGCCAAACTCCTGACCTCACACACACACTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64146809..64146942 26863196 MeRIP-seq:(Medium) rs1258128621 Functional Loss SNV dbSNP153 33..33 33 - - - 56630 RMVar_ID_56630 Human_SNP_ID_469668248 m1A Human chr11 + 64149532 64149532 64149532 AATCACGCCCACAGCCCGGGTGCAGCCTCCGGAGCGCCCCCATTCCATCTGAACCCATCAACACC AATCACGCCCACAGCCCGGGTGCAGCCTCCGGCGCGCCCCCATTCCATCTGAACCCATCAACACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64149527..64149610 26863196 MeRIP-seq:(Medium) rs1481616415 Functional Loss SNV dbSNP153 33..33 33 - - - 56631 RMVar_ID_56631 Human_SNP_ID_469668957 m1A Human chr11 + 64152241 64152241 64152241 GACTAGCTCTTCTTGTCTGCACAATTCTCCCAAGCCACGGGTCTGGAGCCTGCCCACCAGGGCCT GACTAGCTCTTCTTGTCTGCACAATTCTCCCACGCCACGGGTCTGGAGCCTGCCCACCAGGGCCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64152240..64152449 26863196 MeRIP-seq:(Medium) rs373104280 Functional Loss SNV dbSNP153 33..33 33 - - - 56632 RMVar_ID_56632 Human_SNP_ID_469672460 m1A Human chr11 - 64165766 64165766 64165766 CGGCGGCGGTGGGGCGGACAGCCGGGGTGCGCACTTGGGCCCCCCTGGCCATGGCGGCGAAGGTG CGGCGGCGGTGGGGCGGACAGCCGGGGTGCGCCCTTGGGCCCCCCTGGCCATGGCGGCGAAGGTG T G MACROD1 Ensembl:ENSG00000133315 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64165755..64165895 26863410 MeRIP-seq:(Medium) rs1214264402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940659,Human_RBP_ID_4192488,Human_RBP_ID_5138612,Human_RBP_ID_9321514,Human_RBP_ID_17648449,Human_RBP_ID_17668800,Human_RBP_ID_18188534,Human_RBP_ID_18416575,Human_RBP_ID_22569379 Human_Splice_Rec_1252367,Human_Splice_Rec_1252411,Human_Splice_Rec_1252417,Human_Splice_Rec_1252425 RMVar_hsa_circ_79831,RMVar_hsa_circ_150398 56633 RMVar_ID_56633 Human_SNP_ID_469672469 m1A Human chr11 - 64165781 64165781 64165781 TTGGGGCGTGGGGGGCGGCGGCGGTGGGGCGGACAGCCGGGGTGCGCACTTGGGCCCCCCTGGCC TTGGGGCGTGGGGGGCGGCGGCGGTGGGGCGGCCAGCCGGGGTGCGCACTTGGGCCCCCCTGGCC T G MACROD1 Ensembl:ENSG00000133315 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64152228..64166065 26863196 MeRIP-seq:(Medium) rs1055083728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5138612,Human_RBP_ID_9321514,Human_RBP_ID_17648449,Human_RBP_ID_17668800,Human_RBP_ID_18188534,Human_RBP_ID_18416575,Human_RBP_ID_22569379 Human_Splice_Rec_1252367,Human_Splice_Rec_1252411,Human_Splice_Rec_1252417,Human_Splice_Rec_1252425 RMVar_hsa_circ_79831,RMVar_hsa_circ_150398 56634 RMVar_ID_56634 Human_SNP_ID_469672494 m1A Human chr11 + 64165823 64165823 64165823 CGCCGCCGCCCCCCACGCCCCAACTCCCGCCGAGGTCCGCGCACGGCGGCCGAACACGCCCAGGA CGCCGCCGCCCCCCACGCCCCAACTCCCGCCGCGGTCCGCGCACGGCGGCCGAACACGCCCAGGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64165658..64166100 26863196 MeRIP-seq:(Medium) rs1468601751 Functional Loss SNV dbSNP153 33..33 33 - - - 56635 RMVar_ID_56635 Human_SNP_ID_469677271 m1A Human chr11 + 64182872 64182872 64182872 CCCCCTAGGCTTCTCCTCGTCCCATCTCTGACAAGCCTTCACTAACCACTCACCTCTGGGAATGC CCCCCTAGGCTTCTCCTCGTCCCATCTCTGACGAGCCTTCACTAACCACTCACCTCTGGGAATGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64182823..64182935 26863196 MeRIP-seq:(Medium) rs903513744 Functional Loss SNV dbSNP153 33..33 33 - - - 56636 RMVar_ID_56636 Human_SNP_ID_469678499 m1A Human chr11 + 64186237 64186237 64186237 GTTGGGAACGCGGAGCGGACGGATTCGATTCAACGGGGTTCCGGACCGCGCTGCGCTATGGAGCA GTTGGGAACGCGGAGCGGACGGATTCGATTCAGCGGGGTTCCGGACCGCGCTGCGCTATGGAGCA A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64186151..64186439 26863196 MeRIP-seq:(Medium) rs1242322208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31406,Human_RBP_ID_871802,Human_RBP_ID_987792,Human_RBP_ID_1780892,Human_RBP_ID_4185010,Human_RBP_ID_5314231,Human_RBP_ID_5416559,Human_RBP_ID_5436681,Human_RBP_ID_5460586,Human_RBP_ID_5489993,Human_RBP_ID_6084145,Human_RBP_ID_8770753,Human_RBP_ID_8940552,Human_RBP_ID_9004839,Human_RBP_ID_9275008,Human_RBP_ID_9321515,Human_RBP_ID_9362415,Human_RBP_ID_17682331,Human_RBP_ID_17798640,Human_RBP_ID_18188254,Human_RBP_ID_18610198,Human_RBP_ID_22164019,Human_RBP_ID_22895689,Human_RBP_ID_23512223,Human_RBP_ID_26317798,Human_RBP_ID_26803706,Human_RBP_ID_27413545,Human_RBP_ID_27618746,Human_RBP_ID_27803531 Human_Splice_Rec_1252469,Human_Splice_Rec_1252495,Human_Splice_Rec_1252503,Human_Splice_Rec_1252529,Human_Splice_Rec_1252537 RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 56637 RMVar_ID_56637 Human_SNP_ID_469678506 m1A Human chr11 - 64186243 64186243 64186243 TTCACCTGCTCCATAGCGCAGCGCGGTCCGGAACCCCGTTGAATCGAATCCGTCCGCTCCGCGTT TTCACCTGCTCCATAGCGCAGCGCGGTCCGGATCCCCGTTGAATCGAATCCGTCCGCTCCGCGTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64186151..64186780 26863196 MeRIP-seq:(Medium) rs752040686 Functional Loss SNV dbSNP153 33..33 33 - - - 56638 RMVar_ID_56638 Human_SNP_ID_469678507 m1A Human chr11 - 64186244 64186244 64186244 CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGAACCCCGTTGAATCGAATCCGTCCGCTCCGCGT CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGTACCCCGTTGAATCGAATCCGTCCGCTCCGCGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:64186151..64186864;chr11:64186074..64187014 26863196 MeRIP-seq:(Medium) rs1023112598 Functional Loss SNV dbSNP153 33..33 33 - - - 56639 RMVar_ID_56639 Human_SNP_ID_469678508 m1A Human chr11 - 64186244 64186244 64186244 CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGAACCCCGTTGAATCGAATCCGTCCGCTCCGCGT CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGGACCCCGTTGAATCGAATCCGTCCGCTCCGCGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:64186151..64186864;chr11:64186074..64187014 26863196 MeRIP-seq:(Medium) rs1023112598 Functional Loss SNV dbSNP153 33..33 33 - - - 56640 RMVar_ID_56640 Human_SNP_ID_469678509 m1A Human chr11 - 64186244 64186244 64186244 CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGAACCCCGTTGAATCGAATCCGTCCGCTCCGCGT CTTCACCTGCTCCATAGCGCAGCGCGGTCCGGCACCCCGTTGAATCGAATCCGTCCGCTCCGCGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:64186151..64186864;chr11:64186074..64187014 26863196 MeRIP-seq:(Medium) rs1023112598 Functional Loss SNV dbSNP153 33..33 33 - - - 56641 RMVar_ID_56641 Human_SNP_ID_469678534 m1A Human chr11 + 64186269 64186269 64186269 ACGGGGTTCCGGACCGCGCTGCGCTATGGAGCAGGTGAAGGGGGAGGGGCGGGCTGAGGCCCCGA ACGGGGTTCCGGACCGCGCTGCGCTATGGAGCCGGTGAAGGGGGAGGGGCGGGCTGAGGCCCCGA A C STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64186176..64186319 26863410 MeRIP-seq:(Medium) rs1459873797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871802,Human_RBP_ID_1780893,Human_RBP_ID_4185010,Human_RBP_ID_5461038,Human_RBP_ID_8770754,Human_RBP_ID_8940552,Human_RBP_ID_9004840,Human_RBP_ID_9321515,Human_RBP_ID_9362415,Human_RBP_ID_18188254,Human_RBP_ID_22352907,Human_RBP_ID_22435424,Human_RBP_ID_22895689,Human_RBP_ID_23512223,Human_RBP_ID_24363882,Human_RBP_ID_26317798,Human_RBP_ID_26803707,Human_RBP_ID_27803532 Human_Splice_Rec_1252469,Human_Splice_Rec_1252495,Human_Splice_Rec_1252503,Human_Splice_Rec_1252529,Human_Splice_Rec_1252537 RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 56642 RMVar_ID_56642 Human_SNP_ID_469678535 m1A Human chr11 - 64186272 64186272 64186272 GGCTCGGGGCCTCAGCCCGCCCCTCCCCCTTCACCTGCTCCATAGCGCAGCGCGGTCCGGAACCC GGCTCGGGGCCTCAGCCCGCCCCTCCCCCTTCTCCTGCTCCATAGCGCAGCGCGGTCCGGAACCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64186251..64186275 32194978 MeRIP-seq:(Medium) rs112687425 Functional Loss SNV dbSNP153 33..33 33 - - - 56643 RMVar_ID_56643 Human_SNP_ID_469678721 m1A Human chr11 - 64186630 64186630 64186630 CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCACCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCTCCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:64186611..64186769 26863196 MeRIP-seq:(Medium) rs1241119971 Functional Loss SNV dbSNP153 33..33 33 - - - 56644 RMVar_ID_56644 Human_SNP_ID_469678722 m1A Human chr11 - 64186630 64186630 64186630 CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCACCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCCCCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:64186611..64186769 26863196 MeRIP-seq:(Medium) rs1241119971 Functional Loss SNV dbSNP153 33..33 33 - - - 56645 RMVar_ID_56645 Human_SNP_ID_469680854 m1A Human chr11 - 64193016 64193016 64193016 ATGATGTGCCCATTTAATCCCAAGCTTTAAAGACAACACTCATTCTTTCATGTAGTTACCAACAA ATGATGTGCCCATTTAATCCCAAGCTTTAAAGCCAACACTCATTCTTTCATGTAGTTACCAACAA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64193013..64193175 26863410 MeRIP-seq:(Medium) rs748061342 Functional Loss SNV dbSNP153 33..33 33 - - - 56646 RMVar_ID_56646 Human_SNP_ID_469680874 m1A Human chr11 + 64193082 64193082 64193082 GAGAAGCTGTGTGTTCCTTTCCCCTCAGGTCAATGAGCTGAAGGAGAAAGGCAACAAGGCCCTGA GAGAAGCTGTGTGTTCCTTTCCCCTCAGGTCAGTGAGCTGAAGGAGAAAGGCAACAAGGCCCTGA A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64193076..64193337 32194978 MeRIP-seq:(Medium) rs147750881 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_31407,Human_RBP_ID_808621,Human_RBP_ID_871649,Human_RBP_ID_4185011,Human_RBP_ID_5461039,Human_RBP_ID_8774315,Human_RBP_ID_9362416,Human_RBP_ID_18188536,Human_RBP_ID_18610202,Human_RBP_ID_22435425,Human_RBP_ID_24913784,Human_RBP_ID_26317799,Human_RBP_ID_26804840,Human_RBP_ID_26893525,Human_RBP_ID_27804545 Human_Splice_Rec_1252444,Human_Splice_Rec_1252470,Human_Splice_Rec_1252496,Human_Splice_Rec_1252504,Human_Splice_Rec_1252530,Human_Splice_Rec_1252538,Human_Splice_Rec_1252540 RMVar_hsa_circ_109104,RMVar_hsa_circ_150404,RMVar_hsa_circ_303043,RMVar_hsa_circ_311448,RMVar_hsa_circ_322090,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_316317,RMVar_hsa_circ_303371,RMVar_hsa_circ_55185,RMVar_hsa_circ_128188,RMVar_hsa_circ_150406,RMVar_hsa_circ_150407,RMVar_hsa_circ_150405,RMVar_hsa_circ_150403 56647 RMVar_ID_56647 Human_SNP_ID_469680897 m1A Human chr11 + 64193140 64193140 64193140 GCCCTGAGCGTGGGTAACATCGATGATGCCTTACAGTGCTACTCCGAAGCTATTAAGCTGGATCC GCCCTGAGCGTGGGTAACATCGATGATGCCTTGCAGTGCTACTCCGAAGCTATTAAGCTGGATCC A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64193025..64193202 26863196 MeRIP-seq:(Medium) rs184037690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31407,Human_RBP_ID_399750,Human_RBP_ID_1458596,Human_RBP_ID_1780900,Human_RBP_ID_4168566,Human_RBP_ID_8354805,Human_RBP_ID_9362417,Human_RBP_ID_18610203,Human_RBP_ID_26803709,Human_RBP_ID_26893526,Human_RBP_ID_27204046 Human_Splice_Rec_1252444,Human_Splice_Rec_1252470,Human_Splice_Rec_1252496,Human_Splice_Rec_1252504,Human_Splice_Rec_1252530,Human_Splice_Rec_1252538,Human_Splice_Rec_1252540 RMVar_hsa_circ_109104,RMVar_hsa_circ_150404,RMVar_hsa_circ_303043,RMVar_hsa_circ_311448,RMVar_hsa_circ_322090,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_316317,RMVar_hsa_circ_303371,RMVar_hsa_circ_55185,RMVar_hsa_circ_128188,RMVar_hsa_circ_150406,RMVar_hsa_circ_150407,RMVar_hsa_circ_150405,RMVar_hsa_circ_150403 56648 RMVar_ID_56648 Human_SNP_ID_469681654 m1A Human chr11 - 64195729 64195729 64195729 TTTTTGGGAGGGGGTGGTGGTGGAGGTGTTGCAATCTCTTCCTCCTCATCCATACTGCCCAGATC TTTTTGGGAGGGGGTGGTGGTGGAGGTGTTGCGATCTCTTCCTCCTCATCCATACTGCCCAGATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64195679..64195860 26863196 MeRIP-seq:(Medium) rs190514739 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 56649 RMVar_ID_56649 Human_SNP_ID_469683081 m1A Human chr11 - 64199992 64199992 64199992 ACTCGTTGCCTTTGTTCTTCTCCTCCAAAGCCAGGTCGGGGTTTATGTAGGCCAGCCGCTCTTGC ACTCGTTGCCTTTGTTCTTCTCCTCCAAAGCCCGGTCGGGGTTTATGTAGGCCAGCCGCTCTTGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64199942..64200074 26863196 MeRIP-seq:(Medium) rs1170989130 Functional Loss SNV dbSNP153 33..33 33 - - - 56650 RMVar_ID_56650 Human_SNP_ID_469684183 m1A Human chr11 + 64203469 64203469 64203469 TTCTGGACTGCAGGAGGCGGCAGACGGCTACCAGCGCTGTATGATGGCGCAGTACAACCGGCACG TTCTGGACTGCAGGAGGCGGCAGACGGCTACCGGCGCTGTATGATGGCGCAGTACAACCGGCACG A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64203452..64203552 32194978 MeRIP-seq:(Medium) rs1294368902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9275845,Human_RBP_ID_22736432 Human_Splice_Rec_1252466,Human_Splice_Rec_1252492,Human_Splice_Rec_1252526,Human_Splice_Rec_1252574 Human_miRNA_ID_2094346,Human_miRNA_ID_2711296,Human_miRNA_ID_2718411,Human_miRNA_ID_2871548 RMVar_hsa_circ_109104,RMVar_hsa_circ_92848,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_128188,RMVar_hsa_circ_150407,RMVar_hsa_circ_96407,RMVar_hsa_circ_59829,RMVar_hsa_circ_115382,RMVar_hsa_circ_150409,RMVar_hsa_circ_150411,RMVar_hsa_circ_86974,RMVar_hsa_circ_124256,RMVar_hsa_circ_150412,RMVar_hsa_circ_150414,RMVar_hsa_circ_97306,RMVar_hsa_circ_150415,RMVar_hsa_circ_94190,RMVar_hsa_circ_150418,RMVar_hsa_circ_95802,RMVar_hsa_circ_128152,RMVar_hsa_circ_150419,RMVar_hsa_circ_150422,RMVar_hsa_circ_89292,RMVar_hsa_circ_109814,RMVar_hsa_circ_150423,RMVar_hsa_circ_337832,RMVar_hsa_circ_150424,RMVar_hsa_circ_368936,RMVar_hsa_circ_150425,RMVar_hsa_circ_150426 56651 RMVar_ID_56651 Human_SNP_ID_469684211 m1A Human chr11 + 64203524 64203524 64203524 AACCGGCACGACAGCCCCGAAGATGTGAAGCGACGAGCCATGGCCGACCCTGAGGTGCAGCAGAT AACCGGCACGACAGCCCCGAAGATGTGAAGCGGCGAGCCATGGCCGACCCTGAGGTGCAGCAGAT A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64203453..64203657 26863196 MeRIP-seq:(Medium) rs758533538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226993,Human_RBP_ID_399761,Human_RBP_ID_807419,Human_RBP_ID_1780927,Human_RBP_ID_4168633,Human_RBP_ID_6084192,Human_RBP_ID_9275846,Human_RBP_ID_9362439,Human_RBP_ID_11666868,Human_RBP_ID_26317805,Human_RBP_ID_26893570 Human_Splice_Rec_1252466,Human_Splice_Rec_1252467,Human_Splice_Rec_1252492,Human_Splice_Rec_1252493,Human_Splice_Rec_1252500,Human_Splice_Rec_1252501,Human_Splice_Rec_1252526,Human_Splice_Rec_1252527,Human_Splice_Rec_1252574 RMVar_hsa_circ_109104,RMVar_hsa_circ_92848,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_128188,RMVar_hsa_circ_150407,RMVar_hsa_circ_96407,RMVar_hsa_circ_59829,RMVar_hsa_circ_115382,RMVar_hsa_circ_150409,RMVar_hsa_circ_150411,RMVar_hsa_circ_86974,RMVar_hsa_circ_124256,RMVar_hsa_circ_150412,RMVar_hsa_circ_150414,RMVar_hsa_circ_97306,RMVar_hsa_circ_150415,RMVar_hsa_circ_94190,RMVar_hsa_circ_150418,RMVar_hsa_circ_95802,RMVar_hsa_circ_128152,RMVar_hsa_circ_150419,RMVar_hsa_circ_150422,RMVar_hsa_circ_89292,RMVar_hsa_circ_109814,RMVar_hsa_circ_150423,RMVar_hsa_circ_337832,RMVar_hsa_circ_150424,RMVar_hsa_circ_368936,RMVar_hsa_circ_150425,RMVar_hsa_circ_150426 56652 RMVar_ID_56652 Human_SNP_ID_469684218 m1A Human chr11 + 64203550 64203550 64203550 GAAGCGACGAGCCATGGCCGACCCTGAGGTGCAGCAGATCATGAGTGACCCAGCCATGCGCCTTA GAAGCGACGAGCCATGGCCGACCCTGAGGTGCGGCAGATCATGAGTGACCCAGCCATGCGCCTTA A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64202871..64203550 32194978 MeRIP-seq:(Medium) rs1463635827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399761,Human_RBP_ID_871875,Human_RBP_ID_1780927,Human_RBP_ID_6084193,Human_RBP_ID_9275846,Human_RBP_ID_9362439,Human_RBP_ID_11666869,Human_RBP_ID_17649656,Human_RBP_ID_23512299,Human_RBP_ID_26320052,Human_RBP_ID_27204074 Human_Splice_Rec_1252467,Human_Splice_Rec_1252493,Human_Splice_Rec_1252500,Human_Splice_Rec_1252501,Human_Splice_Rec_1252527 Human_miRNA_ID_2617664,Human_miRNA_ID_2750725,Human_miRNA_ID_2996401 RMVar_hsa_circ_109104,RMVar_hsa_circ_92848,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_128188,RMVar_hsa_circ_150407,RMVar_hsa_circ_96407,RMVar_hsa_circ_59829,RMVar_hsa_circ_115382,RMVar_hsa_circ_150409,RMVar_hsa_circ_150411,RMVar_hsa_circ_86974,RMVar_hsa_circ_124256,RMVar_hsa_circ_150412,RMVar_hsa_circ_150414,RMVar_hsa_circ_97306,RMVar_hsa_circ_150415,RMVar_hsa_circ_94190,RMVar_hsa_circ_150418,RMVar_hsa_circ_95802,RMVar_hsa_circ_128152,RMVar_hsa_circ_150419,RMVar_hsa_circ_150422,RMVar_hsa_circ_89292,RMVar_hsa_circ_109814,RMVar_hsa_circ_150423,RMVar_hsa_circ_337832,RMVar_hsa_circ_150424,RMVar_hsa_circ_368936,RMVar_hsa_circ_150425,RMVar_hsa_circ_150426 56653 RMVar_ID_56653 Human_SNP_ID_469684479 m1A Human chr11 - 64204245 64204245 64204245 TACGAGTCTCTGTGTCTTCCCCGGGGTTATGTATAAATATAGAGAGATGAGGCCTTCTCTCCCCT TACGAGTCTCTGTGTCTTCCCCGGGGTTATGTGTAAATATAGAGAGATGAGGCCTTCTCTCCCCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:64204195..64204444 32194978 MeRIP-seq:(Medium) rs1565285034 Functional Loss SNV dbSNP153 33..33 33 - - - 56654 RMVar_ID_56654 Human_SNP_ID_469691392 m1A Human chr11 + 64226414 64226414 64226414 GGGGGACATGGGCATTTGGGGCGCCTGAACCCAAGACCTCTGGATGGTAGGGATGCCCGGGCGTC GGGGGACATGGGCATTTGGGGCGCCTGAACCCGAGACCTCTGGATGGTAGGGATGCCCGGGCGTC A G NUDT22 Ensembl:ENSG00000149761 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64226276..64226425 26863196 MeRIP-seq:(Medium) rs1378746259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399784,Human_RBP_ID_867641,Human_RBP_ID_3939289,Human_RBP_ID_4185018,Human_RBP_ID_5416153,Human_RBP_ID_24363884,Human_RBP_ID_27413582 Human_Splice_Rec_1252803,Human_Splice_Rec_1252817,Human_Splice_Rec_1252825 56655 RMVar_ID_56655 Human_SNP_ID_469692991 m1A Human chr11 - 64230793 64230793 64230793 CTACCAAGAGCGCATTGGACCAGGATGGGGCTAGACTTCAAGCACCCGGGGGCAGAGGGAAGGGG CTACCAAGAGCGCATTGGACCAGGATGGGGCTCGACTTCAAGCACCCGGGGGCAGAGGGAAGGGG T G AP001453.2 Ensembl:ENSG00000256116 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64230778..64230936 26863196 MeRIP-seq:(Medium) rs1396585463 Functional Loss SNV dbSNP153 33..33 33 - - - 56656 RMVar_ID_56656 Human_SNP_ID_469692996 m1A Human chr11 - 64230801 64230801 64230801 AAAGGAGGCTACCAAGAGCGCATTGGACCAGGATGGGGCTAGACTTCAAGCACCCGGGGGCAGAG AAAGGAGGCTACCAAGAGCGCATTGGACCAGGGTGGGGCTAGACTTCAAGCACCCGGGGGCAGAG T C AP001453.2 Ensembl:ENSG00000256116 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64230585..64230891 26863196 MeRIP-seq:(Medium) rs1309994732 Functional Loss SNV dbSNP153 33..33 33 - - - 56657 RMVar_ID_56657 Human_SNP_ID_469693044 m1A Human chr11 - 64230905 64230901 64230905 TGCCCGGCGGCCGCTCCGAGGAGCCGGGAGGGAGGGTTGCGGGGCCACAGCCGGCACAGGCGCAG TGCCCGGCGGCCGCTCCGAGGAGCCGGGAGGG____TTGCGGGGCCACAGCCGGCACAGGCGCAG ACCCT A AP001453.2 Ensembl:ENSG00000256116 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64230734..64230932 26863196 MeRIP-seq:(Medium) rs1200735025 Functional Loss DEL dbSNP153 33..36 33 - - - 56658 RMVar_ID_56658 Human_SNP_ID_469693554 m1A Human chr11 - 64232479 64232479 64232479 GGCTGAGCACACGGTATGCCTCGCTCAGCTCCACAAAGCGGCTGTGCAGGCTTGGGTTCCCAGGG GGCTGAGCACACGGTATGCCTCGCTCAGCTCCGCAAAGCGGCTGTGCAGGCTTGGGTTCCCAGGG T C AP001453.2 Ensembl:ENSG00000256116 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64232425..64232524 32194978 MeRIP-seq:(Medium) rs541349768 Functional Loss SNV dbSNP153 33..33 33 - - - 56659 RMVar_ID_56659 Human_SNP_ID_469693587 m1A Human chr11 - 64232537 64232537 64232537 GACTTTGGGGGACTACCTGAGCGGAGCTGGTCATCATAGCTGCGGCGGCTCTGCTCACGGCTGAG GACTTTGGGGGACTACCTGAGCGGAGCTGGTCGTCATAGCTGCGGCGGCTCTGCTCACGGCTGAG T C AP001453.2 Ensembl:ENSG00000256116 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64232487..64232807 26863196 MeRIP-seq:(Medium) rs1219414525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868754,Human_RBP_ID_5552901 56660 RMVar_ID_56660 Human_SNP_ID_469693690 m1A Human chr11 + 64232793 64232788 64232793 GGGGCCCCAGTTGAGGCAGCAGCAACACAAACAAAACAAACAAGTGCTGGGGTACTGCCTCCTCC GGGGCCCCAGTTGAGGCAGCAGCAACAC_____AAACAAACAAGTGCTGGGGTACTGCCTCCTCC CAAACA C DNAJC4 Ensembl:ENSG00000110011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64232743..64232865 26863196 MeRIP-seq:(Medium) rs1462704589 Functional Loss DEL dbSNP153 29..33 33 - - - Human_Splice_Rec_1252868,Human_Splice_Rec_1252869,Human_Splice_Rec_1252884,Human_Splice_Rec_1252890,Human_Splice_Rec_1252891,Human_Splice_Rec_1252894,Human_Splice_Rec_1252900,Human_Splice_Rec_1252904,Human_Splice_Rec_1252908,Human_Splice_Rec_1252909,Human_Splice_Rec_1252916 56661 RMVar_ID_56661 Human_SNP_ID_469693692 m1A Human chr11 + 64232793 64232793 64232793 GGGGCCCCAGTTGAGGCAGCAGCAACACAAACAAAACAAACAAGTGCTGGGGTACTGCCTCCTCC GGGGCCCCAGTTGAGGCAGCAGCAACACAAACGAAACAAACAAGTGCTGGGGTACTGCCTCCTCC A G DNAJC4 Ensembl:ENSG00000110011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64232743..64232865 26863196 MeRIP-seq:(Medium) rs980693338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1252868,Human_Splice_Rec_1252869,Human_Splice_Rec_1252884,Human_Splice_Rec_1252890,Human_Splice_Rec_1252891,Human_Splice_Rec_1252894,Human_Splice_Rec_1252900,Human_Splice_Rec_1252904,Human_Splice_Rec_1252908,Human_Splice_Rec_1252909,Human_Splice_Rec_1252916 56662 RMVar_ID_56662 Human_SNP_ID_469694301 m1A Human chr11 + 64234567 64234567 64234567 CACATGAGCCGCCTGCCCGCCAGCCCGGGCCCAGCCCCCCGCCGCCCCCGCCGTCCCCGCCGCCG CACATGAGCCGCCTGCCCGCCAGCCCGGGCCCCGCCCCCCGCCGCCCCCGCCGTCCCCGCCGCCG A C VEGFB Ensembl:ENSG00000173511 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:64234556..64234917;chr11:64234559..64234900 26863196 MeRIP-seq:(Medium) rs1290614800 Functional Loss SNV dbSNP153 33..33 33 - - - 56663 RMVar_ID_56663 Human_SNP_ID_469694340 m1A Human chr11 - 64234637 64234620 64234637 GCAGCGCAGCGCAGCGCAGCGGAGGCGGCCGGAGGAGCCGGGCGGGCGGGCGGCCGGTGGCGGCG GCAGCGCAGCGCAGCGCAGCGGAGGCGGCCGG_________________GCGGCCGGTGGCGGCG CCCGCCCGCCCGGCTCCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:64234576..64234711 26863196 MeRIP-seq:(Medium) rs1474461801 Functional Loss DEL dbSNP153 33..49 33 - - - 56664 RMVar_ID_56664 Human_SNP_ID_469694345 m1A Human chr11 - 64234634 64234632 64234635 GCGCAGCGCAGCGCAGCGGAGGCGGCCGGAGGAGCCGGGCGGGCGGGCGGCCGGTGGCGGCGGGC GCGCAGCGCAGCGCAGCGGAGGCGGCCGGAG___CCGGGCGGGCGGGCGGCCGGTGGCGGCGGGC GCTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64234517..64235525 26863196 MeRIP-seq:(Medium) rs1296853530 Functional Loss DEL dbSNP153 32..34 33 - - - 56665 RMVar_ID_56665 Human_SNP_ID_469694354 m1A Human chr11 - 64234652 64234652 64234652 GAGCCCTGGGTGCAGGCAGCGCAGCGCAGCGCAGCGGAGGCGGCCGGAGGAGCCGGGCGGGCGGG GAGCCCTGGGTGCAGGCAGCGCAGCGCAGCGCGGCGGAGGCGGCCGGAGGAGCCGGGCGGGCGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEK293T,untreat control chr11:64234522..64234900;chr11:64234551..64234682;chr11:64234551..64234837;chr11:64234501..64234801 26863410 MeRIP-seq:(Medium) rs111991351 Functional Loss SNV dbSNP153 33..33 33 - - - 56666 RMVar_ID_56666 Human_SNP_ID_469695004 m1A Human chr11 + 64236260 64236260 64236260 CCCCCCTGTTCTTCTCCTGAGCACAGATCCTCATGATCCGGTACCCGAGCAGTCAGCTGGGGGAG CCCCCCTGTTCTTCTCCTGAGCACAGATCCTCCTGATCCGGTACCCGAGCAGTCAGCTGGGGGAG A C VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64234786..64237154 32194978 MeRIP-seq:(Medium) rs200892426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399815,Human_RBP_ID_867645,Human_RBP_ID_3940666,Human_RBP_ID_4168758 Human_Splice_Rec_1252924,Human_Splice_Rec_1252925,Human_Splice_Rec_1252936,Human_Splice_Rec_1252937 RMVar_hsa_circ_7888,RMVar_hsa_circ_150439,RMVar_hsa_circ_75723 56667 RMVar_ID_56667 Human_SNP_ID_469696024 m1A Human chr11 + 64237213 64237213 64237213 TTTCAGACCTAAAAAAAAGGACAGTGCTGTGAAGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG TTTCAGACCTAAAAAAAAGGACAGTGCTGTGAGGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG A G VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64236304..64237600 26863196 MeRIP-seq:(Medium) rs772144625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_987803 Human_Splice_Rec_1252926,Human_Splice_Rec_1252927,Human_Splice_Rec_1252938,Human_Splice_Rec_1252939,Human_Splice_Rec_1252943 Human_miRNA_ID_713622,Human_miRNA_ID_793151,Human_miRNA_ID_1515490 RMVar_hsa_circ_7888 56668 RMVar_ID_56668 Human_SNP_ID_469696025 m1A Human chr11 + 64237213 64237213 64237213 TTTCAGACCTAAAAAAAAGGACAGTGCTGTGAAGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG TTTCAGACCTAAAAAAAAGGACAGTGCTGTGATGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG A T VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64236304..64237600 26863196 MeRIP-seq:(Medium) rs772144625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_987803 Human_Splice_Rec_1252926,Human_Splice_Rec_1252927,Human_Splice_Rec_1252938,Human_Splice_Rec_1252939,Human_Splice_Rec_1252943 Human_miRNA_ID_713622,Human_miRNA_ID_793151,Human_miRNA_ID_1515490 RMVar_hsa_circ_7888 56669 RMVar_ID_56669 Human_SNP_ID_469696234 m1A Human chr11 + 64237539 64237526 64237540 CCATCCCACTCCAGCCCCAGGCCCCTCTGCCCACGCTGCACCCAGCACCACCAGCGCCCTGACCC CCATCCCACTCCAGCCCCAG______________GCTGCACCCAGCACCACCAGCGCCCTGACCC GGCCCCTCTGCCCAC G VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64237394..64237675 26863196 MeRIP-seq:(Medium) rs747360941 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_399820,Human_RBP_ID_17350219 Human_Splice_Rec_1252940,Human_Splice_Rec_1252944 RMVar_hsa_circ_7888 56670 RMVar_ID_56670 Human_SNP_ID_469696296 m1A Human chr11 - 64237591 64237591 64237591 CCCTTGGCAACGGAGGAAGCTGCGGCGTCGGCAGCGGCAGCGGCAGGTCCGGGGGTCAGGGCGCT CCCTTGGCAACGGAGGAAGCTGCGGCGTCGGCCGCGGCAGCGGCAGGTCCGGGGGTCAGGGCGCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64237576..64237600 26863196 MeRIP-seq:(Medium) rs747355174 Functional Loss SNV dbSNP153 33..33 33 - - - 56671 RMVar_ID_56671 Human_SNP_ID_469696347 m1A Human chr11 - 64237651 64237651 64237651 AACAAACACCACCCCACAGACGCCTCACCTGCAGGTGTCTGGGTTGAGCTCTAAGCCCCGCCCTT AACAAACACCACCCCACAGACGCCTCACCTGCGGGTGTCTGGGTTGAGCTCTAAGCCCCGCCCTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64237626..64237650 26863196 MeRIP-seq:(Medium) rs987608909 Functional Loss SNV dbSNP153 33..33 33 - - - 56672 RMVar_ID_56672 Human_SNP_ID_469696348 m1A Human chr11 - 64237651 64237651 64237651 AACAAACACCACCCCACAGACGCCTCACCTGCAGGTGTCTGGGTTGAGCTCTAAGCCCCGCCCTT AACAAACACCACCCCACAGACGCCTCACCTGCCGGTGTCTGGGTTGAGCTCTAAGCCCCGCCCTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64237626..64237650 26863196 MeRIP-seq:(Medium) rs987608909 Functional Loss SNV dbSNP153 33..33 33 - - - 56673 RMVar_ID_56673 Human_SNP_ID_469696618 m1A Human chr11 - 64238529 64238529 64238529 GATGATGGCCTCAGGGAGACAAGGGATGGCAGAAGAGCCCTCTGAGAGGCCCAGGTCCTAGAGCA GATGATGGCCTCAGGGAGACAAGGGATGGCAGGAGAGCCCTCTGAGAGGCCCAGGTCCTAGAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64238479..64238566 26863196 MeRIP-seq:(Medium) rs1000845623 Functional Loss SNV dbSNP153 33..33 33 - - - 56674 RMVar_ID_56674 Human_SNP_ID_469697919 m1A Human chr11 + 64243219 64243218 64243220 ATGGTTCCACAGGGGAAGCTGGAAGATGGGACAGAGTTTGACAGCAGCCTGCCCCAGAACCAGCC ATGGTTCCACAGGGGAAGCTGGAAGATGGGAC__AGTTTGACAGCAGCCTGCCCCAGAACCAGCC CAG C AP001453.5,FKBP2 Ensembl:ENSG00000286264,Ensembl:ENSG00000173486 Protein coding,Protein coding 3'UTR,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64243201..64243225 26863196 MeRIP-seq:(Medium) rs753246885 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_399835,Human_RBP_ID_865917,Human_RBP_ID_5111136,Human_RBP_ID_5138938,Human_RBP_ID_5314242,Human_RBP_ID_5342518,Human_RBP_ID_22433711,Human_RBP_ID_22753695,Human_RBP_ID_26804855 Human_Splice_Rec_1252952,Human_Splice_Rec_1252953,Human_Splice_Rec_1252958,Human_Splice_Rec_1252966,Human_Splice_Rec_1252967,Human_Splice_Rec_1252976,Human_Splice_Rec_1252977,Human_Splice_Rec_1252986,Human_Splice_Rec_1252987,Human_Splice_Rec_1252992,Human_Splice_Rec_1252993,Human_Splice_Rec_1253002,Human_Splice_Rec_1253003,Human_Splice_Rec_1253008,Human_Splice_Rec_1253009,Human_Splice_Rec_1253018,Human_Splice_Rec_1253019,Human_Splice_Rec_1253028,Human_Splice_Rec_1253029,Human_Splice_Rec_1253038,Human_Splice_Rec_1253039 56675 RMVar_ID_56675 Human_SNP_ID_469697920 m1A Human chr11 + 64243219 64243219 64243219 ATGGTTCCACAGGGGAAGCTGGAAGATGGGACAGAGTTTGACAGCAGCCTGCCCCAGAACCAGCC ATGGTTCCACAGGGGAAGCTGGAAGATGGGACGGAGTTTGACAGCAGCCTGCCCCAGAACCAGCC A G AP001453.5,FKBP2 Ensembl:ENSG00000286264,Ensembl:ENSG00000173486 Protein coding,Protein coding 3'UTR,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64243201..64243225 26863196 MeRIP-seq:(Medium) rs1291692412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399835,Human_RBP_ID_865917,Human_RBP_ID_5111136,Human_RBP_ID_5138938,Human_RBP_ID_5314242,Human_RBP_ID_5342518,Human_RBP_ID_22433711,Human_RBP_ID_22753695,Human_RBP_ID_26804855 Human_Splice_Rec_1252952,Human_Splice_Rec_1252953,Human_Splice_Rec_1252958,Human_Splice_Rec_1252966,Human_Splice_Rec_1252967,Human_Splice_Rec_1252976,Human_Splice_Rec_1252977,Human_Splice_Rec_1252986,Human_Splice_Rec_1252987,Human_Splice_Rec_1252992,Human_Splice_Rec_1252993,Human_Splice_Rec_1253002,Human_Splice_Rec_1253003,Human_Splice_Rec_1253008,Human_Splice_Rec_1253009,Human_Splice_Rec_1253018,Human_Splice_Rec_1253019,Human_Splice_Rec_1253028,Human_Splice_Rec_1253029,Human_Splice_Rec_1253038,Human_Splice_Rec_1253039 56676 RMVar_ID_56676 Human_SNP_ID_469698341 m1A Human chr11 + 64244568 64244568 64244568 TATAAAAACACAAAAAGTCCCATCAGTTTAATAACAATAAAAAACCCCAAAAGTGGAAAACTGAG TATAAAAACACAAAAAGTCCCATCAGTTTAATGACAATAAAAAACCCCAAAAGTGGAAAACTGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:64244501..64244625;chr11:64244476..64244626 26863196 MeRIP-seq:(Medium) rs1565322893 Functional Loss SNV dbSNP153 33..33 33 - - - 56677 RMVar_ID_56677 Human_SNP_ID_469698342 m1A Human chr11 + 64244576 64244576 64244576 CACAAAAAGTCCCATCAGTTTAATAACAATAAAAAACCCCAAAAGTGGAAAACTGAGGGGGCAGG CACAAAAAGTCCCATCAGTTTAATAACAATAAGAAACCCCAAAAGTGGAAAACTGAGGGGGCAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64244526..64244575 26863196 MeRIP-seq:(Medium) rs1472951046 Functional Loss SNV dbSNP153 33..33 33 - - - 56678 RMVar_ID_56678 Human_SNP_ID_469698571 m1A Human chr11 - 64245155 64245154 64245155 GCGATGGGTTGCCTGAGGCACTGCCCCGGGAAAGTGAGGCTGTGGAGCCAGGCCCTCAAGCCCCA GCGATGGGTTGCCTGAGGCACTGCCCCGGGAA_GTGAGGCTGTGGAGCCAGGCCCTCAAGCCCCA CT C PPP1R14B Ensembl:ENSG00000173457 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64245152..64245275 26863196 MeRIP-seq:(Medium) rs1341699852 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_865919,Human_RBP_ID_5343797,Human_RBP_ID_19049682,Human_RBP_ID_22471229,Human_RBP_ID_22641443,Human_RBP_ID_23255783 RMVar_hsa_circ_77495,RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150441,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445,RMVar_hsa_circ_97629,RMVar_hsa_circ_150444 56679 RMVar_ID_56679 Human_SNP_ID_469698572 m1A Human chr11 - 64245155 64245155 64245155 GCGATGGGTTGCCTGAGGCACTGCCCCGGGAAAGTGAGGCTGTGGAGCCAGGCCCTCAAGCCCCA GCGATGGGTTGCCTGAGGCACTGCCCCGGGAAGGTGAGGCTGTGGAGCCAGGCCCTCAAGCCCCA T C PPP1R14B Ensembl:ENSG00000173457 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64245152..64245275 26863196 MeRIP-seq:(Medium) rs761050396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865919,Human_RBP_ID_5343797,Human_RBP_ID_19049682,Human_RBP_ID_22471229,Human_RBP_ID_22641443,Human_RBP_ID_23255783 RMVar_hsa_circ_77495,RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150441,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445,RMVar_hsa_circ_97629,RMVar_hsa_circ_150444 56680 RMVar_ID_56680 Human_SNP_ID_469698630 m1A Human chr11 - 64245280 64245280 64245280 CCCTCCTCCCCCACCCCCACCCCAGGAAGAGGAGATCCCAGAACTGGAGATTGACGTGGATGAGC CCCTCCTCCCCCACCCCCACCCCAGGAAGAGGGGATCCCAGAACTGGAGATTGACGTGGATGAGC T C PPP1R14B Ensembl:ENSG00000173457 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1414861574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362445 Human_Splice_Rec_1253046,Human_Splice_Rec_1253047,Human_Splice_Rec_1253052,Human_Splice_Rec_1253053,Human_Splice_Rec_1253057 Human_miRNA_ID_2070591,Human_miRNA_ID_2803510 RMVar_hsa_circ_77495,RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150441,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445,RMVar_hsa_circ_97629,RMVar_hsa_circ_150444 56681 RMVar_ID_56681 Human_SNP_ID_469699111 m1A Human chr11 - 64246714 64246714 64246714 CCAGCCGGCGGGCGTCCCGGAGGCGGTGGCGCAGGGAGGGGCCCGACGCTCGCACGTGGCCCCGG CCAGCCGGCGGGCGTCCCGGAGGCGGTGGCGCGGGGAGGGGCCCGACGCTCGCACGTGGCCCCGG T C PPP1R14B Ensembl:ENSG00000173457 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64246574..64246950 26863196 MeRIP-seq:(Medium) rs1160724369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227076,Human_RBP_ID_399855,Human_RBP_ID_750433,Human_RBP_ID_807854,Human_RBP_ID_4168843,Human_RBP_ID_5110479,Human_RBP_ID_5235231,Human_RBP_ID_5461148,Human_RBP_ID_8774331,Human_RBP_ID_9322132,Human_RBP_ID_17649671,Human_RBP_ID_22433714,Human_RBP_ID_22569393 Human_miRNA_ID_2295586 RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445 56682 RMVar_ID_56682 Human_SNP_ID_469699312 m1A Human chr11 - 64247238 64247238 64247238 CGTCTCCTCACCAGACTCCCTGTCTGCACACGATGTCCACTCCCCTGCATTCTCAGATAGCCCCT CGTCTCCTCACCAGACTCCCTGTCTGCACACGGTGTCCACTCCCCTGCATTCTCAGATAGCCCCT T C AP001453.4 Ensembl:ENSG00000257086 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64247234..64247342 26863196 MeRIP-seq:(Medium) rs1001394854 Functional Loss SNV dbSNP153 33..33 33 - - - 56683 RMVar_ID_56683 Human_SNP_ID_469704953 m1A Human chr11 - 64265951 64265951 64265951 GCTCCAGCAGGCTCTGCACCTGTCTGTTCTGGAACTCCTGATACCGCTTTGCCTCGTCCTCCCCC GCTCCAGCAGGCTCTGCACCTGTCTGTTCTGGCACTCCTGATACCGCTTTGCCTCGTCCTCCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64265901..64266055 26863196 MeRIP-seq:(Medium) rs1356245504 Functional Loss SNV dbSNP153 33..33 33 - - - 56684 RMVar_ID_56684 Human_SNP_ID_469705398 m1A Human chr11 + 64267270 64267270 64267270 GGTCCTGCAACAGCTGGCAGAAGAGGAGCCCAAGGTGAGGCCATGGGCGAACAGGTGGGCAGACG GGTCCTGCAACAGCTGGCAGAAGAGGAGCCCAGGGTGAGGCCATGGGCGAACAGGTGGGCAGACG A G PLCB3 Ensembl:ENSG00000149782 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64267226..64267600 26863196 MeRIP-seq:(Medium) rs1439289068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18973945 Human_Splice_Rec_1253132,Human_Splice_Rec_1253133,Human_Splice_Rec_1253192,Human_Splice_Rec_1253193,Human_Splice_Rec_1253250,Human_Splice_Rec_1253251 RMVar_hsa_circ_116930,RMVar_hsa_circ_150454,RMVar_hsa_circ_127446,RMVar_hsa_circ_150460 56685 RMVar_ID_56685 Human_SNP_ID_469705525 m1A Human chr11 + 64267480 64267480 64267480 GGGGGACGGGCCTCTGGTGGCCTGTGCCAGCAACGGTCACGCACCCGGGAGCAGCGGGCACCTGT GGGGGACGGGCCTCTGGTGGCCTGTGCCAGCAGCGGTCACGCACCCGGGAGCAGCGGGCACCTGT A G PLCB3 Ensembl:ENSG00000149782 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64267431..64267561 26863196 MeRIP-seq:(Medium) rs1181075690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940678,Human_RBP_ID_9275855,Human_RBP_ID_18973947 Human_Splice_Rec_1253195 56686 RMVar_ID_56686 Human_SNP_ID_469706315 m1A Human chr11 - 64270002 64270002 64270002 GTCCCATCGGAAGTTTTGGGTTTTCCGCCCACAGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTC GTCCCATCGGAAGTTTTGGGTTTTCCGCCCACGGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTC T C BAD Ensembl:ENSG00000002330 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64269912..64270175 26863196 MeRIP-seq:(Medium) rs1282374145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399878,Human_RBP_ID_26409623 56687 RMVar_ID_56687 Human_SNP_ID_469706316 m1A Human chr11 - 64270002 64270002 64270002 GTCCCATCGGAAGTTTTGGGTTTTCCGCCCACAGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTC GTCCCATCGGAAGTTTTGGGTTTTCCGCCCACCGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTC T G BAD Ensembl:ENSG00000002330 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64269912..64270175 26863196 MeRIP-seq:(Medium) rs1282374145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399878,Human_RBP_ID_26409623 56688 RMVar_ID_56688 Human_SNP_ID_469706462 m1A Human chr11 - 64270235 64270235 64270235 TCTTCCAGTCCTGGTGGGATCGGAACTTGGGCAGGGGAAGCTCCGCCCCCTCCCAGTGACCTTCG TCTTCCAGTCCTGGTGGGATCGGAACTTGGGCGGGGGAAGCTCCGCCCCCTCCCAGTGACCTTCG T C BAD Ensembl:ENSG00000002330 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64270187..64270359 26863196 MeRIP-seq:(Medium) rs1348660780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399884 Human_miRNA_ID_870812,Human_miRNA_ID_871837,Human_miRNA_ID_1231370 56689 RMVar_ID_56689 Human_SNP_ID_469710608 m1A Human chr11 - 64284373 64284373 64284373 CTTGACTACGTAACATCTTGTCCTCACAGCCCAGAGCATGTTCCAGATCCCAGAGTTTGAGCCGA CTTGACTACGTAACATCTTGTCCTCACAGCCCGGAGCATGTTCCAGATCCCAGAGTTTGAGCCGA T C BAD Ensembl:ENSG00000002330 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:64284144..64284700;chr11:64284124..64284407;chr11:64277029..64284411 26863196 MeRIP-seq:(Medium) rs757853078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185037 Human_Splice_Rec_1253264,Human_Splice_Rec_1253272,Human_Splice_Rec_1253284 56690 RMVar_ID_56690 Human_SNP_ID_469711349 m1A Human chr11 + 64286418 64286418 64286418 TCAGCCACAACTTCTTTCCTCCTGAGCGCCCCATCTCCCTCTCTGCACCCTGCAATTCCCACCCC TCAGCCACAACTTCTTTCCTCCTGAGCGCCCCGTCTCCCTCTCTGCACCCTGCAATTCCCACCCC A G GPR137 Ensembl:ENSG00000173264 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64286368..64286514 26863196 MeRIP-seq:(Medium) rs1255577717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18477873,Human_RBP_ID_22491511 56691 RMVar_ID_56691 Human_SNP_ID_469711797 m1A Human chr11 - 64287799 64287799 64287799 AGCAGCAGGGCCCAGGGCTGTGCCCGGCGCCGATGGGAGAGCACAGCACACAGCACGTTCACCAG AGCAGCAGGGCCCAGGGCTGTGCCCGGCGCCGCTGGGAGAGCACAGCACACAGCACGTTCACCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64287759..64287889 26863196 MeRIP-seq:(Medium) rs1490756400 Functional Loss SNV dbSNP153 33..33 33 - - - 56692 RMVar_ID_56692 Human_SNP_ID_469711954 m1A Human chr11 + 64288145 64288145 64288145 CTCTATGCCAGCCGGGCCTGCTACAACCTGACAGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGA CTCTATGCCAGCCGGGCCTGCTACAACCTGACTGCACTGGCCTTGGCCCCCCAGAGCCGGCTGGA A T GPR137 Ensembl:ENSG00000173264 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64287904..64288205 32194978 MeRIP-seq:(Medium) rs375615961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17798709 Human_Splice_Rec_1253294,Human_Splice_Rec_1253306,Human_Splice_Rec_1253307,Human_Splice_Rec_1253318,Human_Splice_Rec_1253319,Human_Splice_Rec_1253336,Human_Splice_Rec_1253368,Human_Splice_Rec_1253386,Human_Splice_Rec_1253387,Human_Splice_Rec_1253398,Human_Splice_Rec_1253399,Human_Splice_Rec_1253414 56693 RMVar_ID_56693 Human_SNP_ID_469712383 m1A Human chr11 - 64289296 64289295 64289296 CAAGGAGCCGGCCAGAGGAGGGGGTAGCCACGACCCCCAGGATCCTGGGCAAGAAGCGGCAGACA CAAGGAGCCGGCCAGAGGAGGGGGTAGCCACG_CCCCCAGGATCCTGGGCAAGAAGCGGCAGACA GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64289246..64289431 26863196 MeRIP-seq:(Medium) rs1226978653 Functional Loss DEL dbSNP153 33..33 33 - - - 56694 RMVar_ID_56694 Human_SNP_ID_469719313 m1A Human chr11 - 64314296 64314296 64314296 CAGGGAAGGGGCCCGGGAAGGGCAGTGGGTCCACCTCCGGCCGCCGCTTGTACTTCTGCCGCCCA CAGGGAAGGGGCCCGGGAAGGGCAGTGGGTCCGCCTCCGGCCGCCGCTTGTACTTCTGCCGCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64314245..64314371 26863196 MeRIP-seq:(Medium) rs1216095750 Functional Loss SNV dbSNP153 33..33 33 - - - 56695 RMVar_ID_56695 Human_SNP_ID_469719632 m1A Human chr11 + 64315223 64315223 64315223 ACTAGTGCGGCGGCTGCAGGCCCTGCGGCTGGAGCGAGAGGAGTATGTTCTACTAAAGGCCTTGG ACTAGTGCGGCGGCTGCAGGCCCTGCGGCTGGCGCGAGAGGAGTATGTTCTACTAAAGGCCTTGG A C ESRRA Ensembl:ENSG00000173153 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64313935..64315849 32194978 MeRIP-seq:(Medium) rs751065133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399925 Human_Splice_Rec_1253545,Human_Splice_Rec_1253557,Human_Splice_Rec_1253577,Human_Splice_Rec_1253587 56696 RMVar_ID_56696 Human_SNP_ID_469719768 m1A Human chr11 - 64315694 64315692 64315694 ATCTTCGATGTGCACAGAGTCTGCAAGAAGAGAGGAATGTGGTGTTGGCCTGGGCTATCTCTGGC ATCTTCGATGTGCACAGAGTCTGCAAGAAGAG__GAATGTGGTGTTGGCCTGGGCTATCTCTGGC CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64315690..64315881 26863196 MeRIP-seq:(Medium) rs1393814419 Functional Loss DEL dbSNP153 33..34 33 - - - 56697 RMVar_ID_56697 Human_SNP_ID_469719833 m1A Human chr11 - 64315813 64315813 64315813 GTGAGCAGCAGCCTGCCCGCCCGCCGCCGCTCAGCACCCCCTCCGGGGCCAGCCCGGCCGGCTTC GTGAGCAGCAGCCTGCCCGCCCGCCGCCGCTCGGCACCCCCTCCGGGGCCAGCCCGGCCGGCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64315774..64315871 26863196 MeRIP-seq:(Medium) rs975803382 Functional Loss SNV dbSNP153 33..33 33 - - - 56698 RMVar_ID_56698 Human_SNP_ID_469720137 m1A Human chr11 + 64316808 64316808 64316808 GGGATACACACGGCAGAATTCGGAAACAGGGTATAGATCAACAAAAATACACAGTCATAACAAGA GGGATACACACGGCAGAATTCGGAAACAGGGTGTAGATCAACAAAAATACACAGTCATAACAAGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64316751..64316875 26863196 MeRIP-seq:(Medium) rs752937694 Functional Loss SNV dbSNP153 33..33 33 - - - 56699 RMVar_ID_56699 Human_SNP_ID_469720142 m1A Human chr11 - 64316813 64316813 64316813 GTTTTTCTTGTTATGACTGTGTATTTTTGTTGATCTATACCCTGTTTCCGAATTCTGCCGTGTGT GTTTTTCTTGTTATGACTGTGTATTTTTGTTGTTCTATACCCTGTTTCCGAATTCTGCCGTGTGT T A TRMT112 Ensembl:ENSG00000173113 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:64316726..64316875 26863196 MeRIP-seq:(Medium) rs1390374798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31489,Human_RBP_ID_274594,Human_RBP_ID_399936,Human_RBP_ID_748795,Human_RBP_ID_1162630,Human_RBP_ID_1354721,Human_RBP_ID_1458631,Human_RBP_ID_1780945,Human_RBP_ID_2274662,Human_RBP_ID_3377560,Human_RBP_ID_5110483,Human_RBP_ID_6084302,Human_RBP_ID_8354909,Human_RBP_ID_8946253,Human_RBP_ID_11667294,Human_RBP_ID_17649150,Human_RBP_ID_18251429,Human_RBP_ID_18610268,Human_RBP_ID_23206986,Human_RBP_ID_23512400,Human_RBP_ID_24403505,Human_RBP_ID_24463219,Human_RBP_ID_26893665,Human_RBP_ID_27204162 Human_miRNA_ID_1222969 RMVar_hsa_circ_98464,RMVar_hsa_circ_113069,RMVar_hsa_circ_90322,RMVar_hsa_circ_93854,RMVar_hsa_circ_150468,RMVar_hsa_circ_150470,RMVar_hsa_circ_150471,RMVar_hsa_circ_150469 56700 RMVar_ID_56700 Human_SNP_ID_469720145 m1A Human chr11 + 64316824 64316823 64316825 AATTCGGAAACAGGGTATAGATCAACAAAAATACACAGTCATAACAAGAAAAACTGGCGCCTGGC AATTCGGAAACAGGGTATAGATCAACAAAAAT__ACAGTCATAACAAGAAAAACTGGCGCCTGGC TAC T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64316754..64316854 32194978 MeRIP-seq:(Medium) rs758006261 Functional Loss DEL dbSNP153 33..34 33 - - - 56701 RMVar_ID_56701 Human_SNP_ID_469720147 m1A Human chr11 + 64316824 64316823 64316824 AATTCGGAAACAGGGTATAGATCAACAAAAATACACAGTCATAACAAGAAAAACTGGCGCCTGGC AATTCGGAAACAGGGTATAGATCAACAAAAAT_CACAGTCATAACAAGAAAAACTGGCGCCTGGC TA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64316754..64316854 32194978 MeRIP-seq:(Medium) rs922765396 Functional Loss DEL dbSNP153 33..33 33 - - - 56702 RMVar_ID_56702 Human_SNP_ID_469720377 m1A Human chr11 + 64317253 64317253 64317253 CCGCATTCCCCGGGATATGCTGGGGCGGGGTAAGGATCCTCACGTTATCGGCCGCCTCCAGGAAC CCGCATTCCCCGGGATATGCTGGGGCGGGGTAGGGATCCTCACGTTATCGGCCGCCTCCAGGAAC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64317251..64317375 26863196 MeRIP-seq:(Medium) rs1328382847 Functional Loss SNV dbSNP153 33..33 33 - - - 56703 RMVar_ID_56703 Human_SNP_ID_469720418 m1A Human chr11 - 64317331 64317331 64317331 CACCGAGGTCCGTATCTGCCCTGTGGAATTCAACCCCAACTTCGTGGCGCGTATGATACCTAAAG CACCGAGGTCCGTATCTGCCCTGTGGAATTCAGCCCCAACTTCGTGGCGCGTATGATACCTAAAG T C TRMT112 Ensembl:ENSG00000173113 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64317251..64317550 26863196 MeRIP-seq:(Medium) rs1202708632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399944,Human_RBP_ID_987816,Human_RBP_ID_1458637,Human_RBP_ID_1780949,Human_RBP_ID_5416161,Human_RBP_ID_5490011,Human_RBP_ID_9004853,Human_RBP_ID_11667311,Human_RBP_ID_22434578,Human_RBP_ID_23512411 Human_Splice_Rec_1253589,Human_Splice_Rec_1253594,Human_Splice_Rec_1253595,Human_Splice_Rec_1253599,Human_Splice_Rec_1253604,Human_Splice_Rec_1253605,Human_Splice_Rec_1253610,Human_Splice_Rec_1253611 RMVar_hsa_circ_113069,RMVar_hsa_circ_90322,RMVar_hsa_circ_150468,RMVar_hsa_circ_150469,RMVar_hsa_circ_346707 56704 RMVar_ID_56704 Human_SNP_ID_469720429 m1A Human chr11 - 64317367 64317367 64317367 GTCCAGTGCTTGCCTAAACTCCTCCGCCCTGCAGGCCACCGAGGTCCGTATCTGCCCTGTGGAAT GTCCAGTGCTTGCCTAAACTCCTCCGCCCTGCGGGCCACCGAGGTCCGTATCTGCCCTGTGGAAT T C TRMT112 Ensembl:ENSG00000173113 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:64317345..64317444 26863410 MeRIP-seq:(Medium) rs998108042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5343804,Human_RBP_ID_22434579,Human_RBP_ID_23512411 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 56705 RMVar_ID_56705 Human_SNP_ID_469720465 m1A Human chr11 - 64317412 64317412 64317412 CCGCCGGCGGCAGTCTTCCCTTTTCGGGCGGGATGGTGGGCCGGGGTCCAGTGCTTGCCTAAACT CCGCCGGCGGCAGTCTTCCCTTTTCGGGCGGGGTGGTGGGCCGGGGTCCAGTGCTTGCCTAAACT T C TRMT112 Ensembl:ENSG00000173113 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64317246..64317550 32194978 MeRIP-seq:(Medium) rs28699214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5343805 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 56706 RMVar_ID_56706 Human_SNP_ID_469720528 m1A Human chr11 - 64317499 64317499 64317499 GCGACATGAAACTGCTTACCCACAATCTGCTGAGCTCGCATGTGCGGGGGGTGGGGTCCCGTGGC GCGACATGAAACTGCTTACCCACAATCTGCTGCGCTCGCATGTGCGGGGGGTGGGGTCCCGTGGC T G TRMT112 Ensembl:ENSG00000173113 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:64317367..64317530 26863196 MeRIP-seq:(Medium) rs745863361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1265169,Human_RBP_ID_4184172,Human_RBP_ID_5110841,Human_RBP_ID_5138632,Human_RBP_ID_5313670,Human_RBP_ID_5436695,Human_RBP_ID_6084310,Human_RBP_ID_8354915,Human_RBP_ID_9321534,Human_RBP_ID_11667317,Human_RBP_ID_17682345,Human_RBP_ID_17798720,Human_RBP_ID_22433080,Human_RBP_ID_23207344,Human_RBP_ID_23512415 Human_Splice_Rec_1253593,Human_Splice_Rec_1253603,Human_Splice_Rec_1253609 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 56707 RMVar_ID_56707 Human_SNP_ID_469720537 m1A Human chr11 - 64317510 64317510 64317510 GAGTTTGTGCGGCGACATGAAACTGCTTACCCACAATCTGCTGAGCTCGCATGTGCGGGGGGTGG GAGTTTGTGCGGCGACATGAAACTGCTTACCCGCAATCTGCTGAGCTCGCATGTGCGGGGGGTGG T C TRMT112 Ensembl:ENSG00000173113 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr11:64317381..64317550;chr11:64317426..64317575;chr11:64317326..64317550 26863196,26863410 MeRIP-seq:(Medium) rs780435157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1265169,Human_RBP_ID_4185043,Human_RBP_ID_5110841,Human_RBP_ID_5138632,Human_RBP_ID_5313670,Human_RBP_ID_5436695,Human_RBP_ID_8354916,Human_RBP_ID_11667317,Human_RBP_ID_17682345,Human_RBP_ID_22433080,Human_RBP_ID_23512417,Human_RBP_ID_26893672 Human_Splice_Rec_1253593,Human_Splice_Rec_1253603,Human_Splice_Rec_1253609 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 56708 RMVar_ID_56708 Human_SNP_ID_469720538 m1A Human chr11 - 64317510 64317510 64317510 GAGTTTGTGCGGCGACATGAAACTGCTTACCCACAATCTGCTGAGCTCGCATGTGCGGGGGGTGG GAGTTTGTGCGGCGACATGAAACTGCTTACCCCCAATCTGCTGAGCTCGCATGTGCGGGGGGTGG T G TRMT112 Ensembl:ENSG00000173113 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr11:64317381..64317550;chr11:64317426..64317575;chr11:64317326..64317550 26863196,26863410 MeRIP-seq:(Medium) rs780435157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1265169,Human_RBP_ID_4185043,Human_RBP_ID_5110841,Human_RBP_ID_5138632,Human_RBP_ID_5313670,Human_RBP_ID_5436695,Human_RBP_ID_8354916,Human_RBP_ID_11667317,Human_RBP_ID_17682345,Human_RBP_ID_22433080,Human_RBP_ID_23512417,Human_RBP_ID_26893672 Human_Splice_Rec_1253593,Human_Splice_Rec_1253603,Human_Splice_Rec_1253609 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 56709 RMVar_ID_56709 Human_SNP_ID_469720813 m1A Human chr11 - 64318232 64318232 64318232 GTATATAGCCCGCTGAGCGTCTCAGGGCGCACACGCCAGCTAGTCCCATACCCGCCCCACGGCCA GTATATAGCCCGCTGAGCGTCTCAGGGCGCACTCGCCAGCTAGTCCCATACCCGCCCCACGGCCA T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:64318135..64318295 26863410 MeRIP-seq:(Medium) rs978559577 Functional Loss SNV dbSNP153 33..33 33 - - - 56710 RMVar_ID_56710 Human_SNP_ID_469720829 m1A Human chr11 + 64318251 64318251 64318251 GGACTAGCTGGCGTGTGCGCCCTGAGACGCTCAGCGGGCTATATACTCGTCGGTGGGGCCGGCGG GGACTAGCTGGCGTGTGCGCCCTGAGACGCTCGGCGGGCTATATACTCGTCGGTGGGGCCGGCGG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:64318150..64318295 26863410 MeRIP-seq:(Medium) rs1403695945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399948,Human_RBP_ID_987817,Human_RBP_ID_4169127,Human_RBP_ID_5110842,Human_RBP_ID_5313671,Human_RBP_ID_5416163,Human_RBP_ID_5460603,Human_RBP_ID_5490012,Human_RBP_ID_9321535,Human_RBP_ID_18610269,Human_RBP_ID_22426137,Human_RBP_ID_22491515,Human_RBP_ID_27204171 56711 RMVar_ID_56711 Human_SNP_ID_469720855 m1A Human chr11 - 64318288 64318288 64318288 TTCACTGTACCGTCTTGCTGCCGCTGCCGCAGACTGACCGCCGGCCCCACCGACGAGTATATAGC TTCACTGTACCGTCTTGCTGCCGCTGCCGCAGTCTGACCGCCGGCCCCACCGACGAGTATATAGC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64318176..64318403 26863196 MeRIP-seq:(Medium) rs757529407 Functional Loss SNV dbSNP153 33..33 33 - - - 56712 RMVar_ID_56712 Human_SNP_ID_469720862 m1A Human chr11 + 64318296 64318296 64318296 CTCGTCGGTGGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTG CTCGTCGGTGGGGCCGGCGGTCAGTCTGCGGCCGCGGCAGCAAGACGGTACAGTGAAGGAGAGTG A C PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr11:64318176..64318350;chr11:64318151..64318351 26863196 MeRIP-seq:(Medium) rs563893744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227603,Human_RBP_ID_987818,Human_RBP_ID_3940680,Human_RBP_ID_4184174,Human_RBP_ID_5313671,Human_RBP_ID_9321535 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 56713 RMVar_ID_56713 Human_SNP_ID_469720863 m1A Human chr11 + 64318296 64318296 64318296 CTCGTCGGTGGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTG CTCGTCGGTGGGGCCGGCGGTCAGTCTGCGGCGGCGGCAGCAAGACGGTACAGTGAAGGAGAGTG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr11:64318176..64318350;chr11:64318151..64318351 26863196 MeRIP-seq:(Medium) rs563893744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227603,Human_RBP_ID_987818,Human_RBP_ID_3940680,Human_RBP_ID_4184174,Human_RBP_ID_5313671,Human_RBP_ID_9321535 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 56714 RMVar_ID_56714 Human_SNP_ID_469720866 m1A Human chr11 + 64318302 64318302 64318302 GGTGGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTGGGCGTC GGTGGGGCCGGCGGTCAGTCTGCGGCAGCGGCGGCAAGACGGTACAGTGAAGGAGAGTGGGCGTC A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64318176..64318460 26863196 MeRIP-seq:(Medium) rs1360531718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227603,Human_RBP_ID_3940680,Human_RBP_ID_4184174,Human_RBP_ID_5313671,Human_RBP_ID_9322142 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 56715 RMVar_ID_56715 Human_SNP_ID_469720868 m1A Human chr11 + 64318305 64318305 64318305 GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCGAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64318151..64318471 26863196 MeRIP-seq:(Medium) rs1301691525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227603,Human_RBP_ID_3940680,Human_RBP_ID_4185045,Human_RBP_ID_5314252,Human_RBP_ID_9322142 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 56716 RMVar_ID_56716 Human_SNP_ID_469720870 m1A Human chr11 + 64318308 64318308 64318308 GCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTGGGCGTCTGGCGG GCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGGCGGTACAGTGAAGGAGAGTGGGCGTCTGGCGG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:64318126..64319909;chr11:64318217..64318312;chr11:64318101..64319896;chr11:64318126..64318461;chr11:64318126..64318445 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs749654926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227603,Human_RBP_ID_4169130,Human_RBP_ID_5314252,Human_RBP_ID_9322142 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 56717 RMVar_ID_56717 Human_SNP_ID_469721658 m1A Human chr11 + 64320672 64320672 64320672 CCCTTTGTTCCCCTTCCTCAGACACACCTGCCAGGGTTTGTGGAGCAGGCTGAGGCTCTGAAGGC CCCTTTGTTCCCCTTCCTCAGACACACCTGCCGGGGTTTGTGGAGCAGGCTGAGGCTCTGAAGGC A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64318151..64321725 32194978 MeRIP-seq:(Medium) rs1204291910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399957,Human_RBP_ID_5345453,Human_RBP_ID_22433723,Human_RBP_ID_22643307 Human_Splice_Rec_1253616 RMVar_hsa_circ_21664,RMVar_hsa_circ_11328,RMVar_hsa_circ_150472 56718 RMVar_ID_56718 Human_SNP_ID_469721836 m1A Human chr11 + 64321057 64321057 64321057 GATGATTCGCTGGTGTCCATCTTTGGGAATCGACGTCTCAAGAGGTAAAAGTGGAGAGTCCTCTG GATGATTCGCTGGTGTCCATCTTTGGGAATCGGCGTCTCAAGAGGTAAAAGTGGAGAGTCCTCTG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1209804460 Functional Loss SNV dbSNP153 33..33 33 - - - 56719 RMVar_ID_56719 Human_SNP_ID_469721839 m1A Human chr11 - 64321060 64321060 64321060 CCACAGAGGACTCTCCACTTTTACCTCTTGAGACGTCGATTCCCAAAGATGGACACCAGCGAATC CCACAGAGGACTCTCCACTTTTACCTCTTGAGGCGTCGATTCCCAAAGATGGACACCAGCGAATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64321001..64321075 26863196 MeRIP-seq:(Medium) rs1190383334 Functional Loss SNV dbSNP153 33..33 33 - - - 56720 RMVar_ID_56720 Human_SNP_ID_469722061 m1A Human chr11 + 64321593 64321593 64321593 CTGGCTGGGCCCCTCTTTCCGGCAGGTTCTCCATGGTGGTACAGGATGGCATAGTGAAGGCCCTG CTGGCTGGGCCCCTCTTTCCGGCAGGTTCTCCGTGGTGGTACAGGATGGCATAGTGAAGGCCCTG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64321576..64321700 32194978 MeRIP-seq:(Medium) rs1290528355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399965,Human_RBP_ID_4169154,Human_RBP_ID_22571219,Human_RBP_ID_22643308,Human_RBP_ID_23512445,Human_RBP_ID_27413614 Human_Splice_Rec_1253622,Human_Splice_Rec_1253630,Human_Splice_Rec_1253636 RMVar_hsa_circ_150472 56721 RMVar_ID_56721 Human_SNP_ID_469722090 m1A Human chr11 - 64321680 64321680 64321680 GAAGTAATCTGGCCCAGGGCCTCAGAGCTGTGAGATGATATTGGGTGCCAGGCTGCAGGTGAGGC GAAGTAATCTGGCCCAGGGCCTCAGAGCTGTGCGATGATATTGGGTGCCAGGCTGCAGGTGAGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64321537..64321775 26863196 MeRIP-seq:(Medium) rs770453917 Functional Loss SNV dbSNP153 33..33 33 - - - 56722 RMVar_ID_56722 Human_SNP_ID_469728588 m1A Human chr11 + 64344166 64344166 64344166 CTTGGCTCCCCCGGCATTAGACTCAGTGCTCGAGGCATCAGCTGAGTGTCCCCAGGCACCTGATT CTTGGCTCCCCCGGCATTAGACTCAGTGCTCGGGGCATCAGCTGAGTGTCCCCAGGCACCTGATT A G CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64344156..64344318 26863196 MeRIP-seq:(Medium) rs900042091 Functional Loss SNV dbSNP153 33..33 33 - - - 56723 RMVar_ID_56723 Human_SNP_ID_469728975 m1A Human chr11 + 64345054 64345054 64345054 GTGGGAGCGTGAGGGGTCCAGGCTGCGGGCCCAGTCGGAGGCCGCCGAGGAACGGATGCAGGTGC GTGGGAGCGTGAGGGGTCCAGGCTGCGGGCCCGGTCGGAGGCCGCCGAGGAACGGATGCAGGTGC A G CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:64344689..64348862;chr11:64344376..64348862 26863196 MeRIP-seq:(Medium) rs1416395496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865133,Human_RBP_ID_3940690,Human_RBP_ID_22895054,Human_RBP_ID_26320069 56724 RMVar_ID_56724 Human_SNP_ID_469730123 m1A Human chr11 + 64349422 64349422 64349422 GCGTGAGCTGGAGCAGGCGGCTCTCGAGCGCCAGGAATTTCTGCGAGAAAAGGAAAGCCAGCACC GCGTGAGCTGGAGCAGGCGGCTCTCGAGCGCCGGGAATTTCTGCGAGAAAAGGAAAGCCAGCACC A G CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64349371..64349622 26863196 MeRIP-seq:(Medium) rs779044368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865134,Human_RBP_ID_26320070,Human_RBP_ID_27803551 Human_Splice_Rec_1253668,Human_Splice_Rec_1253669,Human_Splice_Rec_1253720,Human_Splice_Rec_1253721,Human_Splice_Rec_1253756,Human_Splice_Rec_1253757,Human_Splice_Rec_1253788,Human_Splice_Rec_1253789,Human_Splice_Rec_1253796,Human_Splice_Rec_1253797,Human_Splice_Rec_1253802,Human_Splice_Rec_1253803 RMVar_hsa_circ_63299 56725 RMVar_ID_56725 Human_SNP_ID_469730625 m1A Human chr11 + 64351209 64351209 64351209 GGGGCTGGGGCCCAAAAAGCGTGCGGAGCCTCAGCTGGTGGAGACCCAGAATGTGCGGCTTATTG GGGGCTGGGGCCCAAAAAGCGTGCGGAGCCTCGGCTGGTGGAGACCCAGAATGTGCGGCTTATTG A G CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64351177..64351392 26863196 MeRIP-seq:(Medium) rs1230881593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1253672,Human_Splice_Rec_1253673,Human_Splice_Rec_1253724,Human_Splice_Rec_1253760,Human_Splice_Rec_1253806,Human_Splice_Rec_1253807 56726 RMVar_ID_56726 Human_SNP_ID_469730646 m1A Human chr11 + 64351270 64351270 64351270 ATTGAGGTGGAGCGCAGTGTGAGTGTGGGCCCACAGTGGGCCCTGGGGAGGTGCCCCGTGCAGTG ATTGAGGTGGAGCGCAGTGTGAGTGTGGGCCCGCAGTGGGCCCTGGGGAGGTGCCCCGTGCAGTG A G CCDC88B Ensembl:ENSG00000168071 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64351262..64351435 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5138634,Human_RBP_ID_5313673,Human_RBP_ID_21965769,Human_RBP_ID_22471444,Human_RBP_ID_22643317,Human_RBP_ID_23512451,Human_RBP_ID_27803552 56727 RMVar_ID_56727 Human_SNP_ID_469731170 m1A Human chr11 + 64352857 64352857 64352857 AGATGGGCATCGGCAGCGGGGCCTGGAGGAGGAGCTGCGGAGGCTTCAGAGCGAGCACGACAGGT AGATGGGCATCGGCAGCGGGGCCTGGAGGAGGGGCTGCGGAGGCTTCAGAGCGAGCACGACAGGT A G CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64352704..64352923 26863196 MeRIP-seq:(Medium) rs771007672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3030,Human_RBP_ID_22471448 Human_Splice_Rec_1253679,Human_Splice_Rec_1253729,Human_Splice_Rec_1253765,Human_Splice_Rec_1253813 56728 RMVar_ID_56728 Human_SNP_ID_469731171 m1A Human chr11 + 64352857 64352857 64352857 AGATGGGCATCGGCAGCGGGGCCTGGAGGAGGAGCTGCGGAGGCTTCAGAGCGAGCACGACAGGT AGATGGGCATCGGCAGCGGGGCCTGGAGGAGGTGCTGCGGAGGCTTCAGAGCGAGCACGACAGGT A T CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64352704..64352923 26863196 MeRIP-seq:(Medium) rs771007672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3030,Human_RBP_ID_22471448 Human_Splice_Rec_1253679,Human_Splice_Rec_1253729,Human_Splice_Rec_1253765,Human_Splice_Rec_1253813 56729 RMVar_ID_56729 Human_SNP_ID_469731528 m1A Human chr11 - 64353723 64353723 64353723 CGAGCTTCTGCTTCTCGCGGCGCAGGGCATTAAGCTGGTCCCTGGCAGGAGTGAGAAGGGAGAGG CGAGCTTCTGCTTCTCGCGGCGCAGGGCATTAGGCTGGTCCCTGGCAGGAGTGAGAAGGGAGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64353702..64353808 26863196 MeRIP-seq:(Medium) rs752347512 Functional Loss SNV dbSNP153 33..33 33 - - - 56730 RMVar_ID_56730 Human_SNP_ID_469732269 m1A Human chr11 - 64355588 64355588 64355588 TTGGCATCTGTTTCGTGTTCCTGCAGGGTCTCAGCGGAGTTCTCCCATCCCACACCAGGTCCTGG TTGGCATCTGTTTCGTGTTCCTGCAGGGTCTCTGCGGAGTTCTCCCATCCCACACCAGGTCCTGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64355239..64355688 26863196 MeRIP-seq:(Medium) rs754681349 Functional Loss SNV dbSNP153 33..33 33 - - - 56731 RMVar_ID_56731 Human_SNP_ID_469735953 m1A Human chr11 + 64368917 64368917 64368917 TGGGCGGGGCCTAGCGTTTGATTCGGGGCCCAAAGGGACCAGGGAGGCGCAGGGAGTGGAATTTG TGGGCGGGGCCTAGCGTTTGATTCGGGGCCCAGAGGGACCAGGGAGGCGCAGGGAGTGGAATTTG A G RPS6KA4 Ensembl:ENSG00000162302 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64368890..64368978 26863196 MeRIP-seq:(Medium) rs1440309131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80658,RMVar_hsa_circ_91794,RMVar_hsa_circ_150474,RMVar_hsa_circ_150476,RMVar_hsa_circ_110858,RMVar_hsa_circ_77914,RMVar_hsa_circ_117323,RMVar_hsa_circ_150477,RMVar_hsa_circ_150478,RMVar_hsa_circ_150479,RMVar_hsa_circ_113877,RMVar_hsa_circ_150480 56732 RMVar_ID_56732 Human_SNP_ID_469736281 m1A Human chr11 - 64369824 64369824 64369824 TCGTAGCCCTGCTGCGCCAGCAGCTCGGGGGCAGCGTACTGCAGCGTGAAGCAGGGCGTCTGCAT TCGTAGCCCTGCTGCGCCAGCAGCTCGGGGGCGGCGTACTGCAGCGTGAAGCAGGGCGTCTGCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64369776..64369844 26863196 MeRIP-seq:(Medium) rs762857058 Functional Loss SNV dbSNP153 33..33 33 - - - 56733 RMVar_ID_56733 Human_SNP_ID_469736815 m1A Human chr11 - 64371333 64371333 64371333 AGCTTCTGCTTCCGCCGCTTGGCCAGGGGTGCATTCTCCACGCTCTTCAGGAAGAAGCCCTCCCG AGCTTCTGCTTCCGCCGCTTGGCCAGGGGTGCGTTCTCCACGCTCTTCAGGAAGAAGCCCTCCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64371276..64371500 26863196 MeRIP-seq:(Medium) rs11542299 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 56734 RMVar_ID_56734 Human_SNP_ID_469736912 m1A Human chr11 + 64371479 64371479 64371479 CCGCCGAGCCAACGGCCCCCTGCCCCCCTCCTAATCCCCACCACTGTGACCCCCTTCCCTCATAG CCGCCGAGCCAACGGCCCCCTGCCCCCCTCCTCATCCCCACCACTGTGACCCCCTTCCCTCATAG A C RPS6KA4 Ensembl:ENSG00000162302 Protein coding stop codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64371381..64371546 26863410 MeRIP-seq:(Medium) rs1483940507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18932536,Human_RBP_ID_22569414 Human_miRNA_ID_159750,Human_miRNA_ID_1995826,Human_miRNA_ID_2228321,Human_miRNA_ID_2285766,Human_miRNA_ID_2288764,Human_miRNA_ID_2504301,Human_miRNA_ID_2725801 RMVar_hsa_circ_80658,RMVar_hsa_circ_91794,RMVar_hsa_circ_150474,RMVar_hsa_circ_150476,RMVar_hsa_circ_110858,RMVar_hsa_circ_77914,RMVar_hsa_circ_150477,RMVar_hsa_circ_150479,RMVar_hsa_circ_113877,RMVar_hsa_circ_150480 56735 RMVar_ID_56735 Human_SNP_ID_469736945 m1A Human chr11 + 64371569 64371569 64371569 ACTCCCGGAGGCCTCTGCCTGCGGCTGACCTGATCCCCAAGGGACTGTCCTTTCCTCTCCTACCC ACTCCCGGAGGCCTCTGCCTGCGGCTGACCTGGTCCCCAAGGGACTGTCCTTTCCTCTCCTACCC A G RPS6KA4 Ensembl:ENSG00000162302 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64371523..64371661 26863196 MeRIP-seq:(Medium) rs1435804159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31111,Human_RBP_ID_399980,Human_RBP_ID_18933629,Human_RBP_ID_27413629 Human_miRNA_ID_1186215,Human_miRNA_ID_2210459 RMVar_hsa_circ_80658,RMVar_hsa_circ_91794,RMVar_hsa_circ_150474,RMVar_hsa_circ_150476,RMVar_hsa_circ_110858,RMVar_hsa_circ_77914,RMVar_hsa_circ_150477,RMVar_hsa_circ_150479,RMVar_hsa_circ_113877,RMVar_hsa_circ_150480 56736 RMVar_ID_56736 Human_SNP_ID_469837437 m1A Human chr11 + 64765023 64765023 64765023 TCGCCAGGACGGATGGGAATCCCGAAACCTGGAGATGAACCTACCCTCGGCAACTTTACAAGACT TCGCCAGGACGGATGGGAATCCCGAAACCTGGGGATGAACCTACCCTCGGCAACTTTACAAGACT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64765001..64765025 26863196 MeRIP-seq:(Medium) rs959871172 Functional Loss SNV dbSNP153 33..33 33 - - - 56737 RMVar_ID_56737 Human_SNP_ID_469837651 m1A Human chr11 + 64765516 64765516 64765516 CATGGCTCGGGCCATCGCCGCCGCGGGGAGGGATCCTGGCGGCCCGGTTTGGGGAGAGGCAAAGG CATGGCTCGGGCCATCGCCGCCGCGGGGAGGGGTCCTGGCGGCCCGGTTTGGGGAGAGGCAAAGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64765301..64765675 26863196 MeRIP-seq:(Medium) rs759384487 Functional Loss SNV dbSNP153 33..33 33 - - - 56738 RMVar_ID_56738 Human_SNP_ID_469837972 m1A Human chr11 - 64766153 64766153 64766153 GTGTGACCTTGGGCTTCTTTACCACCCCAGATACGACGACTACCACCACGAGCGCTGGCACAGGG GTGTGACCTTGGGCTTCTTTACCACCCCAGATGCGACGACTACCACCACGAGCGCTGGCACAGGG T C SF1 Ensembl:ENSG00000168066 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64765801..64766642 26863196 MeRIP-seq:(Medium) rs1184786131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4169375,Human_RBP_ID_11667803,Human_RBP_ID_17798808,Human_RBP_ID_19655900 Human_Splice_Rec_1254808,Human_Splice_Rec_1254902,Human_Splice_Rec_1254916,Human_Splice_Rec_1254940,Human_Splice_Rec_1254950 RMVar_hsa_circ_85629,RMVar_hsa_circ_150496 56739 RMVar_ID_56739 Human_SNP_ID_469838257 m1A Human chr11 + 64766961 64766961 64766961 GCCATACTGCTGCTGGGCGGAGGGGGTGGCGGAGGCTGCTGCTGCTGTTGTTGCCATGGGGGAAG GCCATACTGCTGCTGGGCGGAGGGGGTGGCGGGGGCTGCTGCTGCTGTTGTTGCCATGGGGGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64766880..64767100 26863196 MeRIP-seq:(Medium) rs1428950598 Functional Loss SNV dbSNP153 33..33 33 - - - 56740 RMVar_ID_56740 Human_SNP_ID_469838277 m1A Human chr11 + 64767000 64767000 64767000 TGCTGCTGTTGTTGCCATGGGGGAAGAGGACCAGAGGGAGGGGGTGGGGGCTGCCCACTGGGAGG TGCTGCTGTTGTTGCCATGGGGGAAGAGGACCCGAGGGAGGGGGTGGGGGCTGCCCACTGGGAGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64766901..64767099 26863196 MeRIP-seq:(Medium) rs772411379 Functional Loss SNV dbSNP153 33..33 33 - - - 56741 RMVar_ID_56741 Human_SNP_ID_469838278 m1A Human chr11 + 64767000 64767000 64767000 TGCTGCTGTTGTTGCCATGGGGGAAGAGGACCAGAGGGAGGGGGTGGGGGCTGCCCACTGGGAGG TGCTGCTGTTGTTGCCATGGGGGAAGAGGACCGGAGGGAGGGGGTGGGGGCTGCCCACTGGGAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64766901..64767099 26863196 MeRIP-seq:(Medium) rs772411379 Functional Loss SNV dbSNP153 33..33 33 - - - 56742 RMVar_ID_56742 Human_SNP_ID_469838393 m1A Human chr11 - 64767199 64767199 64767199 CCTGTGGGCTCTGGGGTCTATCGCCTGCATCAAGGAAAAGGTAATGGCTGTCTGCTGGCTGTGGG CCTGTGGGCTCTGGGGTCTATCGCCTGCATCATGGAAAAGGTAATGGCTGTCTGCTGGCTGTGGG T A SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64766903..64769049 32194978 MeRIP-seq:(Medium) rs1447739067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_987849,Human_RBP_ID_4169381,Human_RBP_ID_6084450,Human_RBP_ID_8061987,Human_RBP_ID_8354993,Human_RBP_ID_11667815,Human_RBP_ID_17798812,Human_RBP_ID_19655910,Human_RBP_ID_22569422,Human_RBP_ID_22791254 Human_Splice_Rec_1254780,Human_Splice_Rec_1254781,Human_Splice_Rec_1254804,Human_Splice_Rec_1254805,Human_Splice_Rec_1254828,Human_Splice_Rec_1254829,Human_Splice_Rec_1254850,Human_Splice_Rec_1254851,Human_Splice_Rec_1254874,Human_Splice_Rec_1254875,Human_Splice_Rec_1254898,Human_Splice_Rec_1254899,Human_Splice_Rec_1254906,Human_Splice_Rec_1254907,Human_Splice_Rec_1254912,Human_Splice_Rec_1254913,Human_Splice_Rec_1254936,Human_Splice_Rec_1254937,Human_Splice_Rec_1254946,Human_Splice_Rec_1254947,Human_Splice_Rec_1254952,Human_Splice_Rec_1254953 RMVar_hsa_circ_85629,RMVar_hsa_circ_150496 56743 RMVar_ID_56743 Human_SNP_ID_469838572 m1A Human chr11 + 64767639 64767639 64767639 GGCCCTGGTTCATCGGTGGTGGTGGTGGCTGCATCCAAGGGGGTGGGGGTCCATTGGGGTTGTGC GGCCCTGGTTCATCGGTGGTGGTGGTGGCTGCGTCCAAGGGGGTGGGGGTCCATTGGGGTTGTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64767561..64767775 26863196 MeRIP-seq:(Medium) rs1565559298 Functional Loss SNV dbSNP153 33..33 33 - - - 56744 RMVar_ID_56744 Human_SNP_ID_469838579 m1A Human chr11 - 64767656 64767656 64767656 GGTGGACATCCCATGCAGCACAACCCCAATGGACCCCCACCCCCTTGGATGCAGCCACCACCACC GGTGGACATCCCATGCAGCACAACCCCAATGGCCCCCCACCCCCTTGGATGCAGCCACCACCACC T G SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64766864..64768302 26863196 MeRIP-seq:(Medium) rs768932663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32560,Human_RBP_ID_4169385,Human_RBP_ID_6084457,Human_RBP_ID_11667824,Human_RBP_ID_17349028,Human_RBP_ID_17798814,Human_RBP_ID_27413683 Human_Splice_Rec_1254779,Human_Splice_Rec_1254803,Human_Splice_Rec_1254827,Human_Splice_Rec_1254849,Human_Splice_Rec_1254873,Human_Splice_Rec_1254897,Human_Splice_Rec_1254905,Human_Splice_Rec_1254911,Human_Splice_Rec_1254935,Human_Splice_Rec_1254945,Human_Splice_Rec_1254951 56745 RMVar_ID_56745 Human_SNP_ID_469838627 m1A Human chr11 - 64767815 64767815 64767815 TAGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTTCAGAGAGTCG TAGTCTCTCATGTCTACCACCCAGAGCCGCCCCCCCTGGATGAATTCTGGCCCTTCAGAGAGTCG T G SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64767651..64767850 26863196 MeRIP-seq:(Medium) rs1297590797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11667828,Human_RBP_ID_17232730,Human_RBP_ID_17349030,Human_RBP_ID_18610323 Human_Splice_Rec_1254778,Human_Splice_Rec_1254802,Human_Splice_Rec_1254826,Human_Splice_Rec_1254848,Human_Splice_Rec_1254872,Human_Splice_Rec_1254896,Human_Splice_Rec_1254934,Human_Splice_Rec_1254944 Human_miRNA_ID_1335804,Human_miRNA_ID_1352795 56746 RMVar_ID_56746 Human_SNP_ID_469838631 m1A Human chr11 - 64767825 64767825 64767825 TGCTCTCACGTAGTCTCTCATGTCTACCACCCAGAGCCGCCCACCCTGGATGAATTCTGGCCCTT TGCTCTCACGTAGTCTCTCATGTCTACCACCCGGAGCCGCCCACCCTGGATGAATTCTGGCCCTT T C SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64767684..64767850 26863196 MeRIP-seq:(Medium) rs966418134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11667828 Human_Splice_Rec_1254778,Human_Splice_Rec_1254802,Human_Splice_Rec_1254826,Human_Splice_Rec_1254848,Human_Splice_Rec_1254872,Human_Splice_Rec_1254896,Human_Splice_Rec_1254934,Human_Splice_Rec_1254944 56747 RMVar_ID_56747 Human_SNP_ID_469838792 m1A Human chr11 - 64768238 64768238 64768238 TCAGCTCAGGATAAAGCACGGATGGATAAAGAATATTTGTCCCTCATGGCTGAACTGGGTGAAGC TCAGCTCAGGATAAAGCACGGATGGATAAAGAGTATTTGTCCCTCATGGCTGAACTGGGTGAAGC T C SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64768080..64768300 26863196 MeRIP-seq:(Medium) rs146633957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400104,Human_RBP_ID_1458687,Human_RBP_ID_1780978,Human_RBP_ID_5490027,Human_RBP_ID_6084465,Human_RBP_ID_8770809,Human_RBP_ID_11667835,Human_RBP_ID_17465448,Human_RBP_ID_18610328,Human_RBP_ID_23512638 Human_Splice_Rec_1254776,Human_Splice_Rec_1254800,Human_Splice_Rec_1254824,Human_Splice_Rec_1254846,Human_Splice_Rec_1254870,Human_Splice_Rec_1254894,Human_Splice_Rec_1254932,Human_Splice_Rec_1254942,Human_Splice_Rec_1254960 Human_miRNA_ID_826057 56748 RMVar_ID_56748 Human_SNP_ID_469839370 m1A Human chr11 + 64769954 64769954 64769954 CTCTAAAGGAATTCTATATCCTATAGACCAGCAGTTACTCACCTGGGCCCGATGAGCAGCCCCAC CTCTAAAGGAATTCTATATCCTATAGACCAGCCGTTACTCACCTGGGCCCGATGAGCAGCCCCAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64769951..64769975 26863196 MeRIP-seq:(Medium) rs371298606 Functional Loss SNV dbSNP153 33..33 33 - - - 56749 RMVar_ID_56749 Human_SNP_ID_469841368 m1A Human chr11 - 64776618 64776618 64776618 ATGGATTTTGTCTCTGCCTTTTAGACTTCCCAAGTAAGAAGCGGAAGAGGAGCCGCTGGAACCAA ATGGATTTTGTCTCTGCCTTTTAGACTTCCCAGGTAAGAAGCGGAAGAGGAGCCGCTGGAACCAA T C SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64776501..64776650 26863196 MeRIP-seq:(Medium) rs755008600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8246495,Human_RBP_ID_9362474,Human_RBP_ID_18526366,Human_RBP_ID_24362914,Human_RBP_ID_24542405,Human_RBP_ID_24557105,Human_RBP_ID_24913058,Human_RBP_ID_26317807,Human_RBP_ID_27803565 Human_Splice_Rec_1254762,Human_Splice_Rec_1254786,Human_Splice_Rec_1254810,Human_Splice_Rec_1254834,Human_Splice_Rec_1254856,Human_Splice_Rec_1254880,Human_Splice_Rec_1254918,Human_Splice_Rec_1254974,Human_Splice_Rec_1254980,Human_Splice_Rec_1254990,Human_Splice_Rec_1255000,Human_Splice_Rec_1255004,Human_Splice_Rec_1255006 RMVar_hsa_circ_66549,RMVar_hsa_circ_63095 56750 RMVar_ID_56750 Human_SNP_ID_469842087 m1A Human chr11 - 64778126 64778120 64778126 CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCA CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCC______CCCCGGCGCCTCGTACCCGCCGCCGCA GGACGGT G SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64778124..64778241 32194978 MeRIP-seq:(Medium) rs1436924011 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_9321545 Human_Splice_Rec_1254988 56751 RMVar_ID_56751 Human_SNP_ID_469842093 m1A Human chr11 - 64778126 64778126 64778126 CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCA CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCGCCGTCCCCCGGCGCCTCGTACCCGCCGCCGCA T C SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64778124..64778241 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9321545 Human_Splice_Rec_1254988 56752 RMVar_ID_56752 Human_SNP_ID_469842094 m1A Human chr11 - 64778126 64778126 64778126 CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCACCGTCCCCCGGCGCCTCGTACCCGCCGCCGCA CCTCCCCAGCAGCCGCCGCCGCCTCCACCGCCCCCGTCCCCCGGCGCCTCGTACCCGCCGCCGCA T G SF1 Ensembl:ENSG00000168066 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64778124..64778241 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9321545 Human_Splice_Rec_1254988 56753 RMVar_ID_56753 Human_SNP_ID_469842100 m1A Human chr11 + 64778135 64778132 64778135 GGGTACGAGGCGCCGGGGGACGGTGGCGGTGGAGGCGGCGGCGGCTGCTGGGGAGGCGGAGGGGG GGGTACGAGGCGCCGGGGGACGGTGGCGGT___GGCGGCGGCGGCTGCTGGGGAGGCGGAGGGGG TGGA T - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:64778039..64778239 26863410 MeRIP-seq:(Medium) rs1187236452 Functional Loss DEL dbSNP153 31..33 33 - - - 56754 RMVar_ID_56754 Human_SNP_ID_469842290 m1A Human chr11 + 64778418 64778418 64778418 TCGCCATGGCGCCCCCGGGGACAGGCACCGGCACCTGCTTTTCCTCTGCGGCGGCTTCTCCTTCG TCGCCATGGCGCCCCCGGGGACAGGCACCGGCGCCTGCTTTTCCTCTGCGGCGGCTTCTCCTTCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:64778303..64778677;chr11:64777941..64778550;chr11:64777995..64778550 26863196 MeRIP-seq:(Medium) rs1293017515 Functional Loss SNV dbSNP153 33..33 33 - - - 56755 RMVar_ID_56755 Human_SNP_ID_469842293 m1A Human chr11 - 64778421 64778421 64778421 TTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCAGGTGCCGGTGCCTGTCCCCGGGGGCGCCATGG TTGCGAAGGAGAAGCCGCCGCAGAGGAAAAGCCGGTGCCGGTGCCTGTCCCCGGGGGCGCCATGG T G SF1 Ensembl:ENSG00000168066 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:64778293..64778731;chr11:64777922..64778550 26863196 MeRIP-seq:(Medium) rs963070077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400114,Human_RBP_ID_4185050,Human_RBP_ID_9362475,Human_RBP_ID_17798846,Human_RBP_ID_18416862,Human_RBP_ID_22034605,Human_RBP_ID_22791281,Human_RBP_ID_22895692,Human_RBP_ID_24542657,Human_RBP_ID_26318638,Human_RBP_ID_26893810,Human_RBP_ID_27803566 Human_Splice_Rec_1254785,Human_Splice_Rec_1254809,Human_Splice_Rec_1254833,Human_Splice_Rec_1254855,Human_Splice_Rec_1254879,Human_Splice_Rec_1254973,Human_Splice_Rec_1254979,Human_Splice_Rec_1254987,Human_Splice_Rec_1254999,Human_Splice_Rec_1255005 56756 RMVar_ID_56756 Human_SNP_ID_469842315 m1A Human chr11 - 64778457 64778457 64778457 CCGGCAGCGCATTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAA CCGGCAGCGCATTCGGGTCCCCTCCCCCCGGGGGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAA T C SF1 Ensembl:ENSG00000168066 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr11:64778329..64778505;chr11:64778387..64778686 26863410,32194978 MeRIP-seq:(Medium) rs1261009583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227921,Human_RBP_ID_400115,Human_RBP_ID_4185050,Human_RBP_ID_5460608,Human_RBP_ID_5490030,Human_RBP_ID_6084644,Human_RBP_ID_8770823,Human_RBP_ID_9275856,Human_RBP_ID_9363734,Human_RBP_ID_18416862,Human_RBP_ID_22895692,Human_RBP_ID_23512688,Human_RBP_ID_24542657 Human_Splice_Rec_1254785,Human_Splice_Rec_1254809,Human_Splice_Rec_1254833,Human_Splice_Rec_1254855,Human_Splice_Rec_1254879,Human_Splice_Rec_1254973,Human_Splice_Rec_1254979,Human_Splice_Rec_1254987,Human_Splice_Rec_1254999,Human_Splice_Rec_1255005 56757 RMVar_ID_56757 Human_SNP_ID_469842350 m1A Human chr11 + 64778499 64778499 64778499 AGGGGACCCGAATGCGCTGCCGGAGCGCGCGGAGCCCGTCCTCTCACGCGGCGGGCGGCGGCGGC AGGGGACCCGAATGCGCTGCCGGAGCGCGCGGCGCCCGTCCTCTCACGCGGCGGGCGGCGGCGGC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64778280..64778525 26863196 MeRIP-seq:(Medium) rs1354901024 Functional Loss SNV dbSNP153 33..33 33 - - - 56758 RMVar_ID_56758 Human_SNP_ID_469842382 m1A Human chr11 + 64778537 64778537 64778537 TCCTCTCACGCGGCGGGCGGCGGCGGCGCGAGACGCACAAAGAGGGAGGAGAGAGGGCACCGCGG TCCTCTCACGCGGCGGGCGGCGGCGGCGCGAGGCGCACAAAGAGGGAGGAGAGAGGGCACCGCGG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:64778437..64778587 26863410 MeRIP-seq:(Medium) rs540243836 Functional Loss SNV dbSNP153 33..33 33 - - - 56759 RMVar_ID_56759 Human_SNP_ID_469847490 m1A Human chr11 + 64796313 64796313 64796313 GATGCGCTGGGTGAGGCGGTTGGTGGGGATGGAGAGGGGAACCTGTTGCTGTAGCCTCCGCTGCT GATGCGCTGGGTGAGGCGGTTGGTGGGGATGGGGAGGGGAACCTGTTGCTGTAGCCTCCGCTGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64792363..64796314 32194978 MeRIP-seq:(Medium) rs1394804980 Functional Loss SNV dbSNP153 33..33 33 - - - 56760 RMVar_ID_56760 Human_SNP_ID_469848679 m1A Human chr11 - 64799481 64799481 64799481 CAGCTCCTTCACTCTTGTACTCTGGGCCCCCCAGTTCACCAGGTGAAATTTGGCGCCCCACGCAG CAGCTCCTTCACTCTTGTACTCTGGGCCCCCCCGTTCACCAGGTGAAATTTGGCGCCCCACGCAG T G MAP4K2 Ensembl:ENSG00000168067 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64799431..64799657 32194978 MeRIP-seq:(Medium) rs1565621748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22471237 Human_Splice_Rec_1255033,Human_Splice_Rec_1255095,Human_Splice_Rec_1255199,Human_Splice_Rec_1255261,Human_Splice_Rec_1255299,Human_Splice_Rec_1255331 RMVar_hsa_circ_116378,RMVar_hsa_circ_125733,RMVar_hsa_circ_150503,RMVar_hsa_circ_93797,RMVar_hsa_circ_150504,RMVar_hsa_circ_150505 56761 RMVar_ID_56761 Human_SNP_ID_469850782 m1A Human chr11 - 64804770 64804770 64804770 GCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGAGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGG GCGCATAGTGAGCCGAGAGGCCGAGGCGGCCGTGGCCGAGGAGCCGTGGGGCGAGGAAGCCCGGG T A MEN1 Ensembl:ENSG00000133895 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:64804723..64804808;chr11:64804725..64804823 26863196 MeRIP-seq:(Medium) rs1352053477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520778,Human_RBP_ID_22433083 Human_Splice_Rec_1255430,Human_Splice_Rec_1255446,Human_Splice_Rec_1255464,Human_Splice_Rec_1255482,Human_Splice_Rec_1255500,Human_Splice_Rec_1255516,Human_Splice_Rec_1255534,Human_Splice_Rec_1255552,Human_Splice_Rec_1255572,Human_Splice_Rec_1255590,Human_Splice_Rec_1255606,Human_Splice_Rec_1255626,Human_Splice_Rec_1255642,Human_Splice_Rec_1255660,Human_Splice_Rec_1255676 Clinvar_Rec_157 56762 RMVar_ID_56762 Human_SNP_ID_469851575 m1A Human chr11 + 64807044 64807044 64807044 TTGTGGTAGAGGGTGAGTGGGTCTGGCCGGCCAGGGGTGGGCTCCAGCTCCTCTAGATCTGCCAG TTGTGGTAGAGGGTGAGTGGGTCTGGCCGGCCGGGGGTGGGCTCCAGCTCCTCTAGATCTGCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64806210..64807052 32194978 MeRIP-seq:(Medium) rs746655559 Functional Loss SNV dbSNP153 33..33 33 - - - 56763 RMVar_ID_56763 Human_SNP_ID_469852551 m1A Human chr11 - 64809901 64809901 64809901 CGAGCTCACCTTCCAGCCCAGCCCCGCCCCCGACCCGCCTGGCGGCCTCACCTACTTTCCCGTGG CGAGCTCACCTTCCAGCCCAGCCCCGCCCCCGGCCCGCCTGGCGGCCTCACCTACTTTCCCGTGG T C MEN1 Ensembl:ENSG00000133895 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64809739..64810150 26863410 MeRIP-seq:(Medium) rs1220436193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101503,RMVar_hsa_circ_150514 56764 RMVar_ID_56764 Human_SNP_ID_469852777 m1A Human chr11 - 64810361 64810361 64810361 ATTGGGGCTCCTCATTGGGGTGCTTGGGGCGCACCCCATCGGGTACCGGGCGTCCCGGAATTGTG ATTGGGGCTCCTCATTGGGGTGCTTGGGGCGCCCCCCATCGGGTACCGGGCGTCCCGGAATTGTG T G MEN1 Ensembl:ENSG00000133895 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64810350..64810543 26863196 MeRIP-seq:(Medium) rs530377395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226534,Human_RBP_ID_274600,Human_RBP_ID_807508,Human_RBP_ID_865154,Human_RBP_ID_4184178,Human_RBP_ID_5343826,Human_RBP_ID_9322156,Human_RBP_ID_22034608,Human_RBP_ID_22433728 Human_Splice_Rec_1255447,Human_Splice_Rec_1255535 RMVar_hsa_circ_101503,RMVar_hsa_circ_150514 56765 RMVar_ID_56765 Human_SNP_ID_469852801 m1A Human chr11 + 64810449 64810449 64810449 ACTGTGCCCCCGGGGCTGTAAAGTCTGTCCAGAAAGCGCACCCAGGTCAAGCCCCCAAACCCCAA ACTGTGCCCCCGGGGCTGTAAAGTCTGTCCAGGAAGCGCACCCAGGTCAAGCCCCCAAACCCCAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64810329..64810546 26863196 MeRIP-seq:(Medium) rs537037514 Functional Loss SNV dbSNP153 33..33 33 - - - 56766 RMVar_ID_56766 Human_SNP_ID_469852811 m1A Human chr11 - 64810496 64810496 64810496 GATGTAAGCGCGGAGGTGGGCGAGGGGGACCGAGGCCAGGACTCTCCTTGGGGTTTGGGGGCTTG GATGTAAGCGCGGAGGTGGGCGAGGGGGACCGGGGCCAGGACTCTCCTTGGGGTTTGGGGGCTTG T C MEN1 Ensembl:ENSG00000133895 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64810162..64810625 26863196 MeRIP-seq:(Medium) rs953757251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_749551,Human_RBP_ID_807510,Human_RBP_ID_1265191,Human_RBP_ID_4184179,Human_RBP_ID_5416175,Human_RBP_ID_19052039,Human_RBP_ID_27413719 Human_Splice_Rec_1255683 RMVar_hsa_circ_101503,RMVar_hsa_circ_150514 56767 RMVar_ID_56767 Human_SNP_ID_469860883 m1A Human chr11 - 64834887 64834885 64834887 CCACCAAGATGGCAGAGGAGCTGGAGTCCTTGAGGAACGTAGGCACCCAGACGCTCCCTGCCCGG CCACCAAGATGGCAGAGGAGCTGGAGTCCTTG__GAACGTAGGCACCCAGACGCTCCCTGCCCGG CCT C CDC42BPG Ensembl:ENSG00000171219 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64834875..64834988 26863196 MeRIP-seq:(Medium) rs765593305 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1255728,Human_Splice_Rec_1255729 56768 RMVar_ID_56768 Human_SNP_ID_469860998 m1A Human chr11 + 64835110 64835110 64835110 AGTTGCTCTCCGTCTCCCGCCGCTCACCCTCCAGCCGCTGCTTGCTCTCCTGCTCCTGGGCCAGC AGTTGCTCTCCGTCTCCCGCCGCTCACCCTCCGGCCGCTGCTTGCTCTCCTGCTCCTGGGCCAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64835044..64835178 26863196 MeRIP-seq:(Medium) rs1416073697 Functional Loss SNV dbSNP153 33..33 33 - - - 56769 RMVar_ID_56769 Human_SNP_ID_469862256 m1A Human chr11 - 64838065 64838065 64838065 CTACACCTCAGGCAGGTGAGGCTAGTCCTCACACACCTGGTGGGAGGCTCGGGGTTGCCTGACCT CTACACCTCAGGCAGGTGAGGCTAGTCCTCACTCACCTGGTGGGAGGCTCGGGGTTGCCTGACCT T A CDC42BPG Ensembl:ENSG00000171219 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64838063..64838128 26863196 MeRIP-seq:(Medium) rs966230187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1255710 56770 RMVar_ID_56770 Human_SNP_ID_469866841 m1A Human chr11 + 64853773 64853773 64853773 TTGCGCGTCGGAGCCGGTGGGGCGCGGGAGGAAAGGGCAGGGCCCGCGCACGGGGAGCCTGGGCC TTGCGCGTCGGAGCCGGTGGGGCGCGGGAGGAGAGGGCAGGGCCCGCGCACGGGGAGCCTGGGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64853724..64853826 26863196 MeRIP-seq:(Medium) rs1302171623 Functional Loss SNV dbSNP153 33..33 33 - - - 56771 RMVar_ID_56771 Human_SNP_ID_469866842 m1A Human chr11 + 64853774 64853774 64853774 TGCGCGTCGGAGCCGGTGGGGCGCGGGAGGAAAGGGCAGGGCCCGCGCACGGGGAGCCTGGGCCC TGCGCGTCGGAGCCGGTGGGGCGCGGGAGGAAGGGGCAGGGCCCGCGCACGGGGAGCCTGGGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:64853726..64853876 26863196 MeRIP-seq:(Medium) rs1001507908 Functional Loss SNV dbSNP153 33..33 33 - - - 56772 RMVar_ID_56772 Human_SNP_ID_469867037 m1A Human chr11 - 64854316 64854316 64854316 GCGCAGACATGAGTGATGGCGCCCGGCCCCGCACCTGCCATTTGCACGCCCGGCCGGGAGGCAGA GCGCAGACATGAGTGATGGCGCCCGGCCCCGCGCCTGCCATTTGCACGCCCGGCCGGGAGGCAGA T C EHD1 Ensembl:ENSG00000110047 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64854272..64854373 32194978 MeRIP-seq:(Medium) rs758470055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322157,Human_RBP_ID_22433084 Human_miRNA_ID_2180953,Human_miRNA_ID_2183055,Human_miRNA_ID_3065916 RMVar_hsa_circ_150517,RMVar_hsa_circ_89553,RMVar_hsa_circ_97999,RMVar_hsa_circ_150518 56773 RMVar_ID_56773 Human_SNP_ID_469867038 m1A Human chr11 - 64854316 64854316 64854316 GCGCAGACATGAGTGATGGCGCCCGGCCCCGCACCTGCCATTTGCACGCCCGGCCGGGAGGCAGA GCGCAGACATGAGTGATGGCGCCCGGCCCCGCCCCTGCCATTTGCACGCCCGGCCGGGAGGCAGA T G EHD1 Ensembl:ENSG00000110047 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64854272..64854373 32194978 MeRIP-seq:(Medium) rs758470055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322157,Human_RBP_ID_22433084 Human_miRNA_ID_2180953,Human_miRNA_ID_2183055,Human_miRNA_ID_3065916 RMVar_hsa_circ_150517,RMVar_hsa_circ_89553,RMVar_hsa_circ_97999,RMVar_hsa_circ_150518 56774 RMVar_ID_56774 Human_SNP_ID_469867206 m1A Human chr11 + 64854698 64854698 64854698 GTGCCCGAACGGCCCGTTCATGGTGCCGTCAAAGGCGCCGCCCTTGACCACCTGGGAAGGCATCA GTGCCCGAACGGCCCGTTCATGGTGCCGTCAAGGGCGCCGCCCTTGACCACCTGGGAAGGCATCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64854620..64854720 26863410 MeRIP-seq:(Medium) rs1397360498 Functional Loss SNV dbSNP153 33..33 33 - - - 56775 RMVar_ID_56775 Human_SNP_ID_469873276 m1A Human chr11 + 64878166 64878166 64878166 CCGGCACCACGCCCTCAGTGGGGCCGTGCATGACGGCGATGAAGGAGTCGGTGGTGGGCTCGGGC CCGGCACCACGCCCTCAGTGGGGCCGTGCATGTCGGCGATGAAGGAGTCGGTGGTGGGCTCGGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64878118..64878261 26863196 MeRIP-seq:(Medium) rs777987078 Functional Loss SNV dbSNP153 33..33 33 - - - 56776 RMVar_ID_56776 Human_SNP_ID_469873422 m1A Human chr11 + 64878535 64878525 64878536 GCGGCTGAGAGCGGGGCGAGGGTGCGGAGCCGAGGCGGGGCCGGCCGGGGCAGGGAATCGGGAGC GCGGCTGAGAGCGGGGCGAGGGT___________GCGGGGCCGGCCGGGGCAGGGAATCGGGAGC TGCGGAGCCGAG T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:64878451..64878625 26863410 MeRIP-seq:(Medium) rs781344643 Functional Loss DEL dbSNP153 24..34 33 - - - 56777 RMVar_ID_56777 Human_SNP_ID_469873423 m1A Human chr11 - 64878525 64878525 64878525 CCCTGCCCCGGCCGGCCCCGCCTCGGCTCCGCACCCTCGCCCCGCTCTCAGCCGCCGCTCTGCCC CCCTGCCCCGGCCGGCCCCGCCTCGGCTCCGCCCCCTCGCCCCGCTCTCAGCCGCCGCTCTGCCC T G EHD1 Ensembl:ENSG00000110047 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64878393..64878600 26863410 MeRIP-seq:(Medium) rs905628599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752022,Human_RBP_ID_4184180,Human_RBP_ID_9321549 56778 RMVar_ID_56778 Human_SNP_ID_469883606 m1A Human chr11 - 64910914 64910914 64910914 GCACAGCCGTGCAGCTGTCCTGGGAGCTGCGGACGGGCAGTCGGGGCCGGCGGACAACCAGCATG GCACAGCCGTGCAGCTGTCCTGGGAGCTGCGGTCGGGCAGTCGGGGCCGGCGGACAACCAGCATG T A ATG2A Ensembl:ENSG00000110046 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64910801..64910991 26863196 MeRIP-seq:(Medium) rs769732570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939353,Human_RBP_ID_5341558,Human_RBP_ID_18973988,Human_RBP_ID_22736441,Human_RBP_ID_26318654 Human_Splice_Rec_1255862,Human_Splice_Rec_1255942 RMVar_hsa_circ_104637,RMVar_hsa_circ_150524,RMVar_hsa_circ_127078,RMVar_hsa_circ_84441,RMVar_hsa_circ_150529,RMVar_hsa_circ_150530,RMVar_hsa_circ_91819,RMVar_hsa_circ_150534 56779 RMVar_ID_56779 Human_SNP_ID_469883611 m1A Human chr11 + 64910926 64910926 64910926 CCGCCGGCCCCGACTGCCCGTCCGCAGCTCCCAGGACAGCTGCACGGCTGTGCCCGTTAGCCTGC CCGCCGGCCCCGACTGCCCGTCCGCAGCTCCCGGGACAGCTGCACGGCTGTGCCCGTTAGCCTGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:64910876..64911100 26863196 MeRIP-seq:(Medium) rs561143371 Functional Loss SNV dbSNP153 33..33 33 - - - 56780 RMVar_ID_56780 Human_SNP_ID_469884567 m1A Human chr11 + 64913768 64913768 64913768 GGAACCTAGGCTGCGGGTGGGGACCATCCAGCAGCCCCCACTCCCCATCTTCACACCAGTCCACC GGAACCTAGGCTGCGGGTGGGGACCATCCAGCGGCCCCCACTCCCCATCTTCACACCAGTCCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64913764..64913861 26863196 MeRIP-seq:(Medium) rs1243836432 Functional Loss SNV dbSNP153 33..33 33 - - - 56781 RMVar_ID_56781 Human_SNP_ID_469885615 m1A Human chr11 - 64917154 64917154 64917154 GATCGCCGGCGGGCGGCAAGCGGAGGCGGCCCAGGCCCGGCGGTCTCCGAGATGTCACGATGGCT GATCGCCGGCGGGCGGCAAGCGGAGGCGGCCCTGGCCCGGCGGTCTCCGAGATGTCACGATGGCT T A ATG2A Ensembl:ENSG00000110046 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64917064..64917176 26863196 MeRIP-seq:(Medium) rs763023147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185056,Human_RBP_ID_18416580 RMVar_hsa_circ_84441,RMVar_hsa_circ_150530 56782 RMVar_ID_56782 Human_SNP_ID_469910451 m1A Human chr11 - 65013783 65013782 65013784 GGGCCAGTGTAGGCCCCCGTTCCCAGCAACACAGTCCAAATCCTGCTCATCTGGGCCCTCGGCAT GGGCCAGTGTAGGCCCCCGTTCCCAGCAACA__GTCCAAATCCTGCTCATCTGGGCCCTCGGCAT CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65013733..65013817 26863196 MeRIP-seq:(Medium) rs1373309645 Functional Loss DEL dbSNP153 32..33 33 - - - 56783 RMVar_ID_56783 Human_SNP_ID_469911760 m1A Human chr11 + 65018425 65018425 65018425 TCCTGAAGAAGTTCAATGGGGAGGACATCGACACCATCTCCCCAACGCTGGGCTTCAACATCAAG TCCTGAAGAAGTTCAATGGGGAGGACATCGACGCCATCTCCCCAACGCTGGGCTTCAACATCAAG A G ARL2,ARL2-SNX15 Ensembl:ENSG00000213465,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65018376..65018475 32194978 MeRIP-seq:(Medium) rs780868896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400185,Human_RBP_ID_4185060,Human_RBP_ID_5110854,Human_RBP_ID_17649687,Human_RBP_ID_17798876,Human_RBP_ID_26803758 Human_Splice_Rec_1256184,Human_Splice_Rec_1256185,Human_Splice_Rec_1256192,Human_Splice_Rec_1256193,Human_Splice_Rec_1256196,Human_Splice_Rec_1256197,Human_Splice_Rec_1256206,Human_Splice_Rec_1256207,Human_Splice_Rec_1256214,Human_Splice_Rec_1256215 Human_miRNA_ID_2367250,Human_miRNA_ID_3015049 RMVar_hsa_circ_150542,RMVar_hsa_circ_119843 56784 RMVar_ID_56784 Human_SNP_ID_469911829 m1A Human chr11 + 65018641 65018641 65018641 CCCTGCGGTCCTACTGGCGGAACTACTTTGAGAGCACCGATGGCCTCATCTGGGTAGTGGACAGC CCCTGCGGTCCTACTGGCGGAACTACTTTGAGTGCACCGATGGCCTCATCTGGGTAGTGGACAGC A T ARL2,ARL2-SNX15 Ensembl:ENSG00000213465,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs760922486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400188,Human_RBP_ID_1458762,Human_RBP_ID_5110855,Human_RBP_ID_9362477,Human_RBP_ID_17649156,Human_RBP_ID_22433085,Human_RBP_ID_23512775,Human_RBP_ID_26318660 Human_Splice_Rec_1256186,Human_Splice_Rec_1256187,Human_Splice_Rec_1256194,Human_Splice_Rec_1256198,Human_Splice_Rec_1256199,Human_Splice_Rec_1256208,Human_Splice_Rec_1256209,Human_Splice_Rec_1256211,Human_Splice_Rec_1256216,Human_Splice_Rec_1256217 RMVar_hsa_circ_150542,RMVar_hsa_circ_119843,RMVar_hsa_circ_121815,RMVar_hsa_circ_150543 56785 RMVar_ID_56785 Human_SNP_ID_469912751 m1A Human chr11 + 65021846 65021846 65021846 CTCCTGGATGACATTTCCAGCCGCATTTTCACAGCTGACTGAACCACTCCAGATGCCCCCCACCT CTCCTGGATGACATTTCCAGCCGCATTTTCACGGCTGACTGAACCACTCCAGATGCCCCCCACCT A G ARL2,ARL2-SNX15 Ensembl:ENSG00000213465,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65021796..65022072 26863196 MeRIP-seq:(Medium) rs1325627182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400195,Human_RBP_ID_987884,Human_RBP_ID_5110489,Human_RBP_ID_5165649,Human_RBP_ID_8355090,Human_RBP_ID_9004933,Human_RBP_ID_17232757,Human_RBP_ID_17349052,Human_RBP_ID_17465474,Human_RBP_ID_17649157,Human_RBP_ID_18188274,Human_RBP_ID_22433087,Human_RBP_ID_26405438,Human_RBP_ID_26893877 Human_Splice_Rec_1256203 Human_miRNA_ID_2057879,Human_miRNA_ID_2792868 RMVar_hsa_circ_112577,RMVar_hsa_circ_150542,RMVar_hsa_circ_119843,RMVar_hsa_circ_121815,RMVar_hsa_circ_150543,RMVar_hsa_circ_117689,RMVar_hsa_circ_150544,RMVar_hsa_circ_150545 56786 RMVar_ID_56786 Human_SNP_ID_469912848 m1A Human chr11 - 65022145 65022145 65022145 AAGGAGCGGTTTATTTCACAACTGAGTGAAGGATGAGGCCCACAGCCTCGGTAGCAGCAGTAGCA AAGGAGCGGTTTATTTCACAACTGAGTGAAGGTTGAGGCCCACAGCCTCGGTAGCAGCAGTAGCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65022126..65022175 26863196 MeRIP-seq:(Medium) rs1416747209 Functional Loss SNV dbSNP153 33..33 33 - - - 56787 RMVar_ID_56787 Human_SNP_ID_469914270 m1A Human chr11 - 65027519 65027519 65027519 GCCTGGCGGGACATGAAACCGAGCTGGAGCGGAGCGGAGCGCCGGCCTCCACCTCCTCGCCGTCC GCCTGGCGGGACATGAAACCGAGCTGGAGCGGTGCGGAGCGCCGGCCTCCACCTCCTCGCCGTCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65027470..65027586 26863196 MeRIP-seq:(Medium) rs199754202 Functional Loss SNV dbSNP153 33..33 33 - - - 56788 RMVar_ID_56788 Human_SNP_ID_469914271 m1A Human chr11 - 65027519 65027519 65027519 GCCTGGCGGGACATGAAACCGAGCTGGAGCGGAGCGGAGCGCCGGCCTCCACCTCCTCGCCGTCC GCCTGGCGGGACATGAAACCGAGCTGGAGCGGGGCGGAGCGCCGGCCTCCACCTCCTCGCCGTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65027470..65027586 26863196 MeRIP-seq:(Medium) rs199754202 Functional Loss SNV dbSNP153 33..33 33 - - - 56789 RMVar_ID_56789 Human_SNP_ID_469914301 m1A Human chr11 + 65027587 65027587 65027587 GGATGACTTCCTGCGGCACTACACAGTGTCGGACCCCAGGACTCACCCCAAGGGCTACACCGAGT GGATGACTTCCTGCGGCACTACACAGTGTCGGGCCCCAGGACTCACCCCAAGGGCTACACCGAGT A G SNX15,ARL2-SNX15 Ensembl:ENSG00000110025,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65027436..65027607 26863196 MeRIP-seq:(Medium) rs775459814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185061 Human_Splice_Rec_1256219,Human_Splice_Rec_1256233,Human_Splice_Rec_1256247,Human_Splice_Rec_1256255,Human_Splice_Rec_1256265,Human_Splice_Rec_1256273,Human_Splice_Rec_1256285,Human_Splice_Rec_1256297 RMVar_hsa_circ_348398 56790 RMVar_ID_56790 Human_SNP_ID_469915586 m1A Human chr11 + 65032488 65032488 65032488 ACTTCCGCAAGCTGCATGGAGACCTGGCCTACACCCACCGCAACCTCTTCCGCCGCCTCGAGGAG ACTTCCGCAAGCTGCATGGAGACCTGGCCTACGCCCACCGCAACCTCTTCCGCCGCCTCGAGGAG A G SNX15,ARL2-SNX15 Ensembl:ENSG00000110025,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65032395..65032491 26863196 MeRIP-seq:(Medium) rs1271391112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1256222,Human_Splice_Rec_1256223,Human_Splice_Rec_1256236,Human_Splice_Rec_1256237,Human_Splice_Rec_1256250,Human_Splice_Rec_1256251,Human_Splice_Rec_1256258,Human_Splice_Rec_1256259,Human_Splice_Rec_1256266,Human_Splice_Rec_1256267,Human_Splice_Rec_1256276,Human_Splice_Rec_1256277,Human_Splice_Rec_1256288,Human_Splice_Rec_1256289,Human_Splice_Rec_1256300,Human_Splice_Rec_1256301 RMVar_hsa_circ_83825,RMVar_hsa_circ_305461,RMVar_hsa_circ_150546,RMVar_hsa_circ_150547 56791 RMVar_ID_56791 Human_SNP_ID_469917900 m1A Human chr11 - 65040977 65040977 65040977 GAGCGCCAAGTTCAGCTTCGCGCGCTCCCCTTAGTGTTTTTAACGTGTAGCCCGGGCCGCTCCCA GAGCGCCAAGTTCAGCTTCGCGCGCTCCCCTTCGTGTTTTTAACGTGTAGCCCGGGCCGCTCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65040926..65041156 26863196 MeRIP-seq:(Medium) rs1192423089 Functional Loss SNV dbSNP153 33..33 33 - - - 56792 RMVar_ID_56792 Human_SNP_ID_469918056 m1A Human chr11 - 65041262 65041262 65041262 ATGAGGGGGCTGCGGGGAGACGGTGGGCGCTCAGCATCCCGGGGACGGCAGTGCTGCGGGAAGGC ATGAGGGGGCTGCGGGGAGACGGTGGGCGCTCGGCATCCCGGGGACGGCAGTGCTGCGGGAAGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:65040970..65041817;chr11:65041201..65041734 26863196 MeRIP-seq:(Medium) rs964789896 Functional Loss SNV dbSNP153 33..33 33 - - - 56793 RMVar_ID_56793 Human_SNP_ID_469918084 m1A Human chr11 + 65041330 65041326 65041330 CGGCTGCGAGCTGCCCGTGGGCACCTGCCCGGACATGTGCCCGGCCGCCGAGCGCGCCCAGCGCG CGGCTGCGAGCTGCCCGTGGGCACCTGCC____CATGTGCCCGGCCGCCGAGCGCGCCCAGCGCG CCGGA C SAC3D1 Ensembl:ENSG00000168061 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr11:65041244..65041737;chr11:65041294..65041541 26863410,32194978 MeRIP-seq:(Medium) rs758231576 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4185063,Human_RBP_ID_18432987,Human_RBP_ID_22433731 Human_Splice_Rec_1256304 56794 RMVar_ID_56794 Human_SNP_ID_469919182 m1A Human chr11 - 65044278 65044278 65044278 ATCTACCGCCAAGGCCTTGCGGAGGGGCGGGCAGGCGCGCAGGGCAGCAGGCAGCTGTAGAACCT ATCTACCGCCAAGGCCTTGCGGAGGGGCGGGCGGGCGCGCAGGGCAGCAGGCAGCTGTAGAACCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65044205..65044393 26863196 MeRIP-seq:(Medium) rs763382275 Functional Loss SNV dbSNP153 33..33 33 - - - 56795 RMVar_ID_56795 Human_SNP_ID_469919329 m1A Human chr11 - 65044594 65044594 65044594 TGCACGTACTGGCAGGCGGTAGCCCTTCCTCCACGTAGCGACCCCTCAGGAACACAACTCTCTCC TGCACGTACTGGCAGGCGGTAGCCCTTCCTCCGCGTAGCGACCCCTCAGGAACACAACTCTCTCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65044501..65044706 26863196 MeRIP-seq:(Medium) rs976658710 Functional Loss SNV dbSNP153 33..33 33 - - - 56796 RMVar_ID_56796 Human_SNP_ID_469921411 m1A Human chr11 - 65051332 65051332 65051332 ACCCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGGAG ACCCTGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAGAAAGAAAGAAAGGAG T C NAALADL1 Ensembl:ENSG00000168060 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:65051318..65051405 26863410 MeRIP-seq:(Medium) rs1478833448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59292,RMVar_hsa_circ_80470,RMVar_hsa_circ_150550 56797 RMVar_ID_56797 Human_SNP_ID_469928363 m1A Human chr11 + 65078652 65078652 65078652 GAACTGAAAACCTCTTTACACAGGTGGGTTCAAGAAGAAAGCCACCAACAGAAGGCAACTCAGGA GAACTGAAAACCTCTTTACACAGGTGGGTTCAGGAAGAAAGCCACCAACAGAAGGCAACTCAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65078601..65078800 32194978 MeRIP-seq:(Medium) rs1360646716 Functional Loss SNV dbSNP153 33..33 33 - - - 56798 RMVar_ID_56798 Human_SNP_ID_469928711 m1A Human chr11 - 65079647 65079647 65079647 CCGAACCCTGAGGCCGAGTCCAGCTCCAAGGAAGGAGAGCTGGACGCCAGAGACTTGGAAATGTC CCGAACCCTGAGGCCGAGTCCAGCTCCAAGGAGGGAGAGCTGGACGCCAGAGACTTGGAAATGTC T C CDCA5 Ensembl:ENSG00000146670 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65079596..65079742 26863196 MeRIP-seq:(Medium) rs1288456616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400280,Human_RBP_ID_1458808,Human_RBP_ID_4169884,Human_RBP_ID_6084771,Human_RBP_ID_9362479 Human_miRNA_ID_954025 RMVar_hsa_circ_121966,RMVar_hsa_circ_106081,RMVar_hsa_circ_150552,RMVar_hsa_circ_150554,RMVar_hsa_circ_78610,RMVar_hsa_circ_150553,RMVar_hsa_circ_71524,RMVar_hsa_circ_269569,RMVar_hsa_circ_333409,RMVar_hsa_circ_17479 56799 RMVar_ID_56799 Human_SNP_ID_469928718 m1A Human chr11 + 65079671 65079671 65079671 AGCTCTCCTTCCTTGGAGCTGGACTCGGCCTCAGGGTTCGGCACAGGAGTGCTGGTGGGGGTGGC AGCTCTCCTTCCTTGGAGCTGGACTCGGCCTCGGGGTTCGGCACAGGAGTGCTGGTGGGGGTGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65079621..65079777 26863196 MeRIP-seq:(Medium) rs150704124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126966,RMVar_hsa_circ_150556 56800 RMVar_ID_56800 Human_SNP_ID_469928719 m1A Human chr11 + 65079671 65079671 65079671 AGCTCTCCTTCCTTGGAGCTGGACTCGGCCTCAGGGTTCGGCACAGGAGTGCTGGTGGGGGTGGC AGCTCTCCTTCCTTGGAGCTGGACTCGGCCTCTGGGTTCGGCACAGGAGTGCTGGTGGGGGTGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65079621..65079777 26863196 MeRIP-seq:(Medium) rs150704124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126966,RMVar_hsa_circ_150556 56801 RMVar_ID_56801 Human_SNP_ID_469929970 m1A Human chr11 + 65084277 65084277 65084277 ATCGGGGCGGCCGGGGCTGAAGGGAGAGGCGCAGGAGCCCTGGGGAGAGTGGTCCCTGCCCTTCC ATCGGGGCGGCCGGGGCTGAAGGGAGAGGCGCGGGAGCCCTGGGGAGAGTGGTCCCTGCCCTTCC A G ZFPL1 Ensembl:ENSG00000162300 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65084226..65084858;chr11:65084226..65084400 26863196 MeRIP-seq:(Medium) rs1279162333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184184 Human_Splice_Rec_1256709,Human_Splice_Rec_1256751,Human_Splice_Rec_1256763,Human_Splice_Rec_1256773 56802 RMVar_ID_56802 Human_SNP_ID_469929997 m1A Human chr11 - 65084346 65084346 65084346 CCCAGTCTCTGTGTTTACTGATCGGCCGCTGCACTGGTTCCGAAGGGCGGTAGCGATGGCTCGAG CCCAGTCTCTGTGTTTACTGATCGGCCGCTGCGCTGGTTCCGAAGGGCGGTAGCGATGGCTCGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr11:65084226..65084418;chr11:65084251..65084379 26863196 MeRIP-seq:(Medium) rs1052574348 Functional Loss SNV dbSNP153 33..33 33 - - - 56803 RMVar_ID_56803 Human_SNP_ID_469930250 m1A Human chr11 + 65085158 65085158 65085158 GTCCTACCTGCAATGGCTCCAAGATAGCGACTACAACCCCAATTGCCGCCTGTGCAACATACCCC GTCCTACCTGCAATGGCTCCAAGATAGCGACTGCAACCCCAATTGCCGCCTGTGCAACATACCCC A G ZFPL1 Ensembl:ENSG00000162300 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr11:65085119..65085269;chr11:65085119..65085319 26863196,32194978 MeRIP-seq:(Medium) rs1308261715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1256712,Human_Splice_Rec_1256724,Human_Splice_Rec_1256725,Human_Splice_Rec_1256746,Human_Splice_Rec_1256754,Human_Splice_Rec_1256758,Human_Splice_Rec_1256760,Human_Splice_Rec_1256766,Human_Splice_Rec_1256767,Human_Splice_Rec_1256778,Human_Splice_Rec_1256779,Human_Splice_Rec_1256786,Human_Splice_Rec_1256787,Human_Splice_Rec_1256793 RMVar_hsa_circ_52150,RMVar_hsa_circ_77033,RMVar_hsa_circ_19665,RMVar_hsa_circ_150558 56804 RMVar_ID_56804 Human_SNP_ID_469930592 m1A Human chr11 + 65086484 65086484 65086484 CCAGCTACCCCGAAACACGGCACCTGCCGGCTATCAGTGCCCCAGCTGCAATGGCCCCATCTTCC CCAGCTACCCCGAAACACGGCACCTGCCGGCTCTCAGTGCCCCAGCTGCAATGGCCCCATCTTCC A C ZFPL1 Ensembl:ENSG00000162300 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:65086398..65086796;chr11:65086436..65086552 26863196 MeRIP-seq:(Medium) rs748407449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750029,Human_RBP_ID_17350228 Human_Splice_Rec_1256726,Human_Splice_Rec_1256740,Human_Splice_Rec_1256748,Human_Splice_Rec_1256762,Human_Splice_Rec_1256768,Human_Splice_Rec_1256780,Human_Splice_Rec_1256788 Human_miRNA_ID_2012884,Human_miRNA_ID_2684720,Human_miRNA_ID_2759266 RMVar_hsa_circ_52150,RMVar_hsa_circ_77033,RMVar_hsa_circ_150558 56805 RMVar_ID_56805 Human_SNP_ID_469930593 m1A Human chr11 + 65086484 65086484 65086484 CCAGCTACCCCGAAACACGGCACCTGCCGGCTATCAGTGCCCCAGCTGCAATGGCCCCATCTTCC CCAGCTACCCCGAAACACGGCACCTGCCGGCTGTCAGTGCCCCAGCTGCAATGGCCCCATCTTCC A G ZFPL1 Ensembl:ENSG00000162300 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:65086398..65086796;chr11:65086436..65086552 26863196 MeRIP-seq:(Medium) rs748407449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750029,Human_RBP_ID_17350228 Human_Splice_Rec_1256726,Human_Splice_Rec_1256740,Human_Splice_Rec_1256748,Human_Splice_Rec_1256762,Human_Splice_Rec_1256768,Human_Splice_Rec_1256780,Human_Splice_Rec_1256788 Human_miRNA_ID_2012884,Human_miRNA_ID_2684720,Human_miRNA_ID_2759266 RMVar_hsa_circ_52150,RMVar_hsa_circ_77033,RMVar_hsa_circ_150558 56806 RMVar_ID_56806 Human_SNP_ID_469931118 m1A Human chr11 - 65088021 65088021 65088021 GCTGCGGCCCGGCCTAGGCGAGACATGAGGGCAAGGAGGGCCAGGAAGCCCAGCAGTCCCAAGAG GCTGCGGCCCGGCCTAGGCGAGACATGAGGGCGAGGAGGGCCAGGAAGCCCAGCAGTCCCAAGAG T C TMEM262 Ensembl:ENSG00000187066 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65087923..65088024 32194978 MeRIP-seq:(Medium) rs1171215152 Functional Loss SNV dbSNP153 33..33 33 - - - 56807 RMVar_ID_56807 Human_SNP_ID_469933435 m1A Human chr11 - 65096423 65096423 65096423 CGAAGTGCGCCCCGTTCAGATCAGTCGGGTCCAGGGGGTCGGGCCCCGCGGGGCGTCCCGCCGCC CGAAGTGCGCCCCGTTCAGATCAGTCGGGTCCGGGGGGTCGGGCCCCGCGGGGCGTCCCGCCGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65096324..65096500 26863410 MeRIP-seq:(Medium) rs1286263929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17798933 56808 RMVar_ID_56808 Human_SNP_ID_469936744 m1A Human chr11 + 65109393 65109393 65109393 TGCGACAGCCCTGGGGAGAAGGGGGGTGCCACACCACCTGCCCTGCTCCTGCTGCTCTCCCGCCT TGCGACAGCCCTGGGGAGAAGGGGGGTGCCACCCCACCTGCCCTGCTCCTGCTGCTCTCCCGCCT A C VPS51 Ensembl:ENSG00000149823 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65109276..65109507 32194978 MeRIP-seq:(Medium) rs1016874861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808688,Human_RBP_ID_18188284,Human_RBP_ID_23512911 Human_miRNA_ID_377272,Human_miRNA_ID_484001,Human_miRNA_ID_832137,Human_miRNA_ID_1237851,Human_miRNA_ID_2221942,Human_miRNA_ID_2484999 RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_104693,RMVar_hsa_circ_150561,RMVar_hsa_circ_150563,RMVar_hsa_circ_114050,RMVar_hsa_circ_150562,RMVar_hsa_circ_123532,RMVar_hsa_circ_150564,RMVar_hsa_circ_150566,RMVar_hsa_circ_77042,RMVar_hsa_circ_126166,RMVar_hsa_circ_150567 56809 RMVar_ID_56809 Human_SNP_ID_469937161 m1A Human chr11 + 65110533 65110530 65110534 AGGGTGTTCGCAAGGCCCAGAGCAGCGACTCCAGCAAGAGGACTTTCTCCGTGTACAGCAGCTCT AGGGTGTTCGCAAGGCCCAGAGCAGCGACT____CAAGAGGACTTTCTCCGTGTACAGCAGCTCT TCCAG T VPS51 Ensembl:ENSG00000149823 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65110476..65110756 32194978 MeRIP-seq:(Medium) rs1407835651 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_21883053 Human_Splice_Rec_1256852,Human_Splice_Rec_1256853,Human_Splice_Rec_1256908,Human_Splice_Rec_1256909,Human_Splice_Rec_1256918,Human_Splice_Rec_1256919,Human_Splice_Rec_1256925,Human_Splice_Rec_1256932,Human_Splice_Rec_1256933,Human_Splice_Rec_1256935 RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_104693,RMVar_hsa_circ_150561,RMVar_hsa_circ_52511,RMVar_hsa_circ_150563,RMVar_hsa_circ_114050,RMVar_hsa_circ_150562,RMVar_hsa_circ_123532,RMVar_hsa_circ_150564,RMVar_hsa_circ_150566,RMVar_hsa_circ_77042,RMVar_hsa_circ_126166,RMVar_hsa_circ_150567,RMVar_hsa_circ_118913,RMVar_hsa_circ_122403,RMVar_hsa_circ_150568,RMVar_hsa_circ_75710,RMVar_hsa_circ_150569,RMVar_hsa_circ_150570 56810 RMVar_ID_56810 Human_SNP_ID_469937162 m1A Human chr11 + 65110533 65110533 65110533 AGGGTGTTCGCAAGGCCCAGAGCAGCGACTCCAGCAAGAGGACTTTCTCCGTGTACAGCAGCTCT AGGGTGTTCGCAAGGCCCAGAGCAGCGACTCCGGCAAGAGGACTTTCTCCGTGTACAGCAGCTCT A G VPS51 Ensembl:ENSG00000149823 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65110476..65110756 32194978 MeRIP-seq:(Medium) rs762891136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21883053 Human_Splice_Rec_1256852,Human_Splice_Rec_1256853,Human_Splice_Rec_1256908,Human_Splice_Rec_1256909,Human_Splice_Rec_1256918,Human_Splice_Rec_1256919,Human_Splice_Rec_1256925,Human_Splice_Rec_1256932,Human_Splice_Rec_1256933,Human_Splice_Rec_1256935 RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_104693,RMVar_hsa_circ_150561,RMVar_hsa_circ_52511,RMVar_hsa_circ_150563,RMVar_hsa_circ_114050,RMVar_hsa_circ_150562,RMVar_hsa_circ_123532,RMVar_hsa_circ_150564,RMVar_hsa_circ_150566,RMVar_hsa_circ_77042,RMVar_hsa_circ_126166,RMVar_hsa_circ_150567,RMVar_hsa_circ_118913,RMVar_hsa_circ_122403,RMVar_hsa_circ_150568,RMVar_hsa_circ_75710,RMVar_hsa_circ_150569,RMVar_hsa_circ_150570 56811 RMVar_ID_56811 Human_SNP_ID_469938117 m1A Human chr11 + 65112933 65112933 65112933 CGGCCGGGGGTGGAGCTCCAGGCCTAGCGGGGAGGTCCACGGAGATTGGCCCCCACCCCAGGCTC CGGCCGGGGGTGGAGCTCCAGGCCTAGCGGGGGGGTCCACGGAGATTGGCCCCCACCCCAGGCTC A G TM7SF2 Ensembl:ENSG00000149809 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65112930..65113030 32194978 MeRIP-seq:(Medium) rs1433118436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18972185,Human_RBP_ID_23255902 56812 RMVar_ID_56812 Human_SNP_ID_469938754 m1A Human chr11 + 65115001 65115001 65115001 GTTTGGGGACATGGCCTGGGTGCCCTTCACCTACAGCCTGCAGGCCCAGTTCCTGCTGCACCACC GTTTGGGGACATGGCCTGGGTGCCCTTCACCTGCAGCCTGCAGGCCCAGTTCCTGCTGCACCACC A G TM7SF2 Ensembl:ENSG00000149809 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65114903..65115002 32194978 MeRIP-seq:(Medium) rs375674215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4170044,Human_RBP_ID_22433737,Human_RBP_ID_26803770 Human_Splice_Rec_1256948,Human_Splice_Rec_1256949,Human_Splice_Rec_1256962,Human_Splice_Rec_1256975,Human_Splice_Rec_1256986,Human_Splice_Rec_1256987,Human_Splice_Rec_1257000,Human_Splice_Rec_1257001,Human_Splice_Rec_1257018,Human_Splice_Rec_1257019,Human_Splice_Rec_1257036,Human_Splice_Rec_1257037,Human_Splice_Rec_1257050,Human_Splice_Rec_1257051,Human_Splice_Rec_1257064,Human_Splice_Rec_1257065,Human_Splice_Rec_1257076,Human_Splice_Rec_1257077,Human_Splice_Rec_1257098,Human_Splice_Rec_1257106,Human_Splice_Rec_1257107,Human_Splice_Rec_1257130,Human_Splice_Rec_1257142,Human_Splice_Rec_1257150,Human_Splice_Rec_1257151,Human_Splice_Rec_1257164,Human_Splice_Rec_1257165,Human_Splice_Rec_1257170,Human_Splice_Rec_1257171,Human_Splice_Rec_1257178,Human_Splice_Rec_1257179,Human_Splice_Rec_1257190 Human_miRNA_ID_1156924,Human_miRNA_ID_3088333 RMVar_hsa_circ_18910,RMVar_hsa_circ_50214,RMVar_hsa_circ_104461,RMVar_hsa_circ_150574,RMVar_hsa_circ_150575,RMVar_hsa_circ_325706 56813 RMVar_ID_56813 Human_SNP_ID_469939665 m1A Human chr11 + 65117025 65117025 65117025 CGAACAGCACATTGGGCAGCTGGAAGCGCACGAGCGGCGAGACTGGGCCGCGGCTCAGGCTGACT CGAACAGCACATTGGGCAGCTGGAAGCGCACGGGCGGCGAGACTGGGCCGCGGCTCAGGCTGACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65116984..65117625 26863196 MeRIP-seq:(Medium) rs1444398248 Functional Loss SNV dbSNP153 33..33 33 - - - 56814 RMVar_ID_56814 Human_SNP_ID_469939702 m1A Human chr11 - 65117089 65117089 65117089 AGCGGGTTCTTGGAGATGTCCCGGGGGCCTGCACGCCCGTCGTACCCACCCGCATCCCCGCGATA AGCGGGTTCTTGGAGATGTCCCGGGGGCCTGCGCGCCCGTCGTACCCACCCGCATCCCCGCGATA T C ZNHIT2 Ensembl:ENSG00000174276 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65116991..65117260 26863196 MeRIP-seq:(Medium) rs892615165 Functional Loss SNV dbSNP153 33..33 33 - - - 56815 RMVar_ID_56815 Human_SNP_ID_469940980 m1A Human chr11 - 65120791 65120791 65120791 AACCTTCCCTTCTCCAGGTGGCCAAACAGGAGAAGAAGAAGAAGAAGACAGGTCGGGCTAAGCGG AACCTTCCCTTCTCCAGGTGGCCAAACAGGAGGAGAAGAAGAAGAAGACAGGTCGGGCTAAGCGG T C FAU Ensembl:ENSG00000149806 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1200469527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400322,Human_RBP_ID_1458831,Human_RBP_ID_1781083,Human_RBP_ID_3377691,Human_RBP_ID_18610457 Human_Splice_Rec_1257202,Human_Splice_Rec_1257210,Human_Splice_Rec_1257216,Human_Splice_Rec_1257224,Human_Splice_Rec_1257230,Human_Splice_Rec_1257240 RMVar_hsa_circ_84951,RMVar_hsa_circ_100979,RMVar_hsa_circ_110524,RMVar_hsa_circ_92527,RMVar_hsa_circ_150579,RMVar_hsa_circ_150581,RMVar_hsa_circ_76363,RMVar_hsa_circ_150582,RMVar_hsa_circ_150580,RMVar_hsa_circ_150578 56816 RMVar_ID_56816 Human_SNP_ID_469941136 m1A Human chr11 + 65121448 65121448 65121448 TGTGACACTCAGCTGTCAGGACTATGCACCCCACACTCACTAGACGCTTACCGGTACTTCAAAGA TGTGACACTCAGCTGTCAGGACTATGCACCCCCCACTCACTAGACGCTTACCGGTACTTCAAAGA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:65121443..65121725 26863196 MeRIP-seq:(Medium) rs1451206746 Functional Loss SNV dbSNP153 33..33 33 - - - 56817 RMVar_ID_56817 Human_SNP_ID_469941140 m1A Human chr11 + 65121457 65121453 65121457 CAGCTGTCAGGACTATGCACCCCACACTCACTAGACGCTTACCGGTACTTCAAAGAACATTCCTC CAGCTGTCAGGACTATGCACCCCACACTC____GACGCTTACCGGTACTTCAAAGAACATTCCTC CACTA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65121454..65121875 26863410 MeRIP-seq:(Medium) rs1476278341 Functional Loss DEL dbSNP153 30..33 33 - - - 56818 RMVar_ID_56818 Human_SNP_ID_469941188 m1A Human chr11 + 65121559 65121559 65121559 GGGTAGTCAGGGCCTCCACCCCGCACTGGCCCAGAGTGGCCTCATCCTCCAGGGGCGCGCCTGCC GGGTAGTCAGGGCCTCCACCCCGCACTGGCCCGGAGTGGCCTCATCCTCCAGGGGCGCGCCTGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65121475..65121825 32194978 MeRIP-seq:(Medium) rs932409557 Functional Loss SNV dbSNP153 33..33 33 - - - 56819 RMVar_ID_56819 Human_SNP_ID_469941385 m1A Human chr11 + 65122082 65122082 65122082 GCTACAAGCCCTTCGGATCCAGCCAAGGCCCCATTCTTACCTGAACGGCGGTCCCAGCTACCGCG GCTACAAGCCCTTCGGATCCAGCCAAGGCCCCGTTCTTACCTGAACGGCGGTCCCAGCTACCGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65122076..65122175 26863196 MeRIP-seq:(Medium) rs1377165492 Functional Loss SNV dbSNP153 33..33 33 - - - 56820 RMVar_ID_56820 Human_SNP_ID_469941543 m1A Human chr11 - 65122370 65122370 65122370 CGCTGGACACCGGTTCTCCATCCCCGCAGCGTAGCCCGGAACATGGTAGCTGCCATCTTTACCTG CGCTGGACACCGGTTCTCCATCCCCGCAGCGTGGCCCGGAACATGGTAGCTGCCATCTTTACCTG T C SYVN1 Ensembl:ENSG00000162298 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65122326..65124739 26863196 MeRIP-seq:(Medium) rs770601478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1257246 56821 RMVar_ID_56821 Human_SNP_ID_469941552 m1A Human chr11 + 65122389 65122389 65122389 CCATGTTCCGGGCTACGCTGCGGGGATGGAGAACCGGTGTCCAGCGGGGCTGCGGGCTACGGCTG CCATGTTCCGGGCTACGCTGCGGGGATGGAGACCCGGTGTCCAGCGGGGCTGCGGGCTACGGCTG A C MRPL49 Ensembl:ENSG00000149792 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65122340..65122461 26863196 MeRIP-seq:(Medium) rs762571917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_274602,Human_RBP_ID_4185073,Human_RBP_ID_5314282,Human_RBP_ID_5341576,Human_RBP_ID_6084852,Human_RBP_ID_8355170,Human_RBP_ID_18416582,Human_RBP_ID_18610463,Human_RBP_ID_19049779,Human_RBP_ID_22433091,Human_RBP_ID_23206990,Human_RBP_ID_27804603 Human_Splice_Rec_1257483,Human_Splice_Rec_1257487,Human_Splice_Rec_1257495,Human_Splice_Rec_1257499,Human_Splice_Rec_1257505,Human_Splice_Rec_1257509 56822 RMVar_ID_56822 Human_SNP_ID_469943376 m1A Human chr11 + 65128596 65128596 65128596 TGGAGGCCTTTCCATTTCAGGGGCTGGTGGGGAGGCTCCTGGGGTTGGGGTCGTGGCCTCTGAGC TGGAGGCCTTTCCATTTCAGGGGCTGGTGGGGTGGCTCCTGGGGTTGGGGTCGTGGCCTCTGAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65128320..65128725 26863196 MeRIP-seq:(Medium) rs578230352 Functional Loss SNV dbSNP153 33..33 33 - - - 56823 RMVar_ID_56823 Human_SNP_ID_469944778 m1A Human chr11 - 65132950 65132950 65132950 CTTCACTCTTCTTCTCTTCCTCAAATGTTTCCACTGGCTGGCTGAGGACCGTGTGGACTTTGTGA CTTCACTCTTCTTCTCTTCCTCAAATGTTTCCTCTGGCTGGCTGAGGACCGTGTGGACTTTGTGA T A SYVN1 Ensembl:ENSG00000162298 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65132926..65132950 26863196 MeRIP-seq:(Medium) rs1478411745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750026,Human_RBP_ID_18432993,Human_RBP_ID_18972195,Human_RBP_ID_22433748,Human_RBP_ID_22753704,Human_RBP_ID_27413860 Human_Splice_Rec_1257255,Human_Splice_Rec_1257285,Human_Splice_Rec_1257315,Human_Splice_Rec_1257341,Human_Splice_Rec_1257363,Human_Splice_Rec_1257405,Human_Splice_Rec_1257421,Human_Splice_Rec_1257433,Human_Splice_Rec_1257443,Human_Splice_Rec_1257459,Human_Splice_Rec_1257469,Human_Splice_Rec_1257471 Human_miRNA_ID_883128,Human_miRNA_ID_2397735 RMVar_hsa_circ_2171,RMVar_hsa_circ_120755,RMVar_hsa_circ_368048,RMVar_hsa_circ_150585 56824 RMVar_ID_56824 Human_SNP_ID_469945248 m1A Human chr11 - 65134501 65134501 65134501 AGGGGGTGGGGAGTGTTGTTAACCGGAGGGGCAGCCGCAGTCGCGCGGATTGAGCGGGCTCGCGG AGGGGGTGGGGAGTGTTGTTAACCGGAGGGGCGGCCGCAGTCGCGCGGATTGAGCGGGCTCGCGG T C SYVN1 Ensembl:ENSG00000162298 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65134401..65134525 26863196 MeRIP-seq:(Medium) rs1350171966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751437,Human_RBP_ID_4184194,Human_RBP_ID_17668802,Human_RBP_ID_18416866 Human_Splice_Rec_1257249,Human_Splice_Rec_1257279,Human_Splice_Rec_1257309,Human_Splice_Rec_1257335,Human_Splice_Rec_1257453 56825 RMVar_ID_56825 Human_SNP_ID_469962365 m1A Human chr11 + 65204758 65204758 65204758 GACGGATGACCCGGACGACTACGGGGACCGCGAGTCAGGCTGCAGCTTCGTGCTCGCCCTTATGC GACGGATGACCCGGACGACTACGGGGACCGCGCGTCAGGCTGCAGCTTCGTGCTCGCCCTTATGC A C CAPN1 Ensembl:ENSG00000014216 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65204676..65204850 32194978 MeRIP-seq:(Medium) rs764022910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867708,Human_RBP_ID_18972207,Human_RBP_ID_22433102 Human_Splice_Rec_1257564,Human_Splice_Rec_1257622,Human_Splice_Rec_1257664,Human_Splice_Rec_1257718,Human_Splice_Rec_1257810,Human_Splice_Rec_1257848,Human_Splice_Rec_1257856 Human_miRNA_ID_2454044,Human_miRNA_ID_2454045,Human_miRNA_ID_2454046 RMVar_hsa_circ_150587,RMVar_hsa_circ_102811,RMVar_hsa_circ_125191,RMVar_hsa_circ_150588,RMVar_hsa_circ_83684,RMVar_hsa_circ_150589,RMVar_hsa_circ_79907,RMVar_hsa_circ_150590,RMVar_hsa_circ_88052,RMVar_hsa_circ_82525,RMVar_hsa_circ_113151,RMVar_hsa_circ_150592,RMVar_hsa_circ_150593,RMVar_hsa_circ_150594 56826 RMVar_ID_56826 Human_SNP_ID_469978219 m1A Human chr11 - 65262259 65262259 65262259 GTCGCCCAAGCCAGGGGCCGGGGAGCCGGCCCACCCAGCTCCGACCTGCGCCCAAGAAGCCCACG GTCGCCCAAGCCAGGGGCCGGGGAGCCGGCCCCCCCAGCTCCGACCTGCGCCCAAGAAGCCCACG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65262209..65262310 32194978 MeRIP-seq:(Medium) rs1317680224 Functional Loss SNV dbSNP153 33..33 33 - - - 56827 RMVar_ID_56827 Human_SNP_ID_469982736 m1A Human chr11 - 65280999 65280999 65280999 TGCTATCACAGCCAATCTGGCCCAGCAGAGTGACAGGCTCCTACCAAAGGAAGGTCACAGCATAA TGCTATCACAGCCAATCTGGCCCAGCAGAGTGGCAGGCTCCTACCAAAGGAAGGTCACAGCATAA T C lnc-SLC25A45-3 RNACentral:URS0000D59F9A lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65280987..65281137 32194978 MeRIP-seq:(Medium) rs1256027881 Functional Loss SNV dbSNP153 33..33 33 - - - 56828 RMVar_ID_56828 Human_SNP_ID_469985937 m1A Human chr11 + 65294640 65294638 65294641 ATCCACAGATCTGCTTTTCCACCTGGGGGCCGAGGAGATCAGTAGGTAAGAAGTGTGTTCCAGGC ATCCACAGATCTGCTTTTCCACCTGGGGGCC___GAGATCAGTAGGTAAGAAGTGTGTTCCAGGC CGAG C AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65287783..65294665 32194978 MeRIP-seq:(Medium) rs762683711 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_226177,Human_RBP_ID_865198,Human_RBP_ID_18974050,Human_RBP_ID_26803779 Human_Splice_Rec_1257984,Human_Splice_Rec_1257985,Human_Splice_Rec_1258028,Human_Splice_Rec_1258029,Human_Splice_Rec_1258056,Human_Splice_Rec_1258057,Human_Splice_Rec_1258072,Human_Splice_Rec_1258073,Human_Splice_Rec_1258086,Human_Splice_Rec_1258088,Human_Splice_Rec_1258089,Human_Splice_Rec_1258122,Human_Splice_Rec_1258123 RMVar_hsa_circ_39511,RMVar_hsa_circ_96374,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_373934,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_295786,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819,RMVar_hsa_circ_150617,RMVar_hsa_circ_150618,RMVar_hsa_circ_124891,RMVar_hsa_circ_280844,RMVar_hsa_circ_51650,RMVar_hsa_circ_150619 56829 RMVar_ID_56829 Human_SNP_ID_469987591 m1A Human chr11 + 65301489 65301489 65301489 GTCTGTTGGGGCAGGTCGGGAGGAAGAGGGGCACCAAGTGGGCCATTGGAATACTGGAAGCAGCA GTCTGTTGGGGCAGGTCGGGAGGAAGAGGGGCTCCAAGTGGGCCATTGGAATACTGGAAGCAGCA A T AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65301441..65301684 26863196 MeRIP-seq:(Medium) rs938694287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3387875,Human_RBP_ID_8174399,Human_RBP_ID_9414993,Human_RBP_ID_18477900 56830 RMVar_ID_56830 Human_SNP_ID_469990841 m1A Human chr11 - 65314912 65314912 65314912 GCAGACGGCAGACCGGCGGACAGCAAGGTCTCAGGAGCTGGACAGCGCGGCGGCCGGACCCGACC GCAGACGGCAGACCGGCGGACAGCAAGGTCTCGGGAGCTGGACAGCGCGGCGGCCGGACCCGACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65314906..65315018 26863196 MeRIP-seq:(Medium) rs1165141727 Functional Loss SNV dbSNP153 33..33 33 - - - 56831 RMVar_ID_56831 Human_SNP_ID_469992483 m1A Human chr11 + 65321198 65321198 65321198 ACCGTGTGTGGGCGGGAGCTCCCGGACGGCCCATCCCCTCTGCTCAAGAACGCCATCTCCCTCCC ACCGTGTGTGGGCGGGAGCTCCCGGACGGCCCGTCCCCTCTGCTCAAGAACGCCATCTCCCTCCC A G AP000944.5,CDC42EP2 Ensembl:ENSG00000285816,Ensembl:ENSG00000149798 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65321193..65321293 26863196 MeRIP-seq:(Medium) rs1317002301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27413925 Human_miRNA_ID_2272858,Human_miRNA_ID_2865609 RMVar_hsa_circ_113846,RMVar_hsa_circ_150623 56832 RMVar_ID_56832 Human_SNP_ID_469992656 m1A Human chr11 - 65321653 65321653 65321653 GAGGGAGAGGGGAAACACGGCTCAGAAGGAGAATCACTGGCCAGCGACCATACAGGTGGGATCTT GAGGGAGAGGGGAAACACGGCTCAGAAGGAGACTCACTGGCCAGCGACCATACAGGTGGGATCTT T G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65321551..65321725 26863410 MeRIP-seq:(Medium) rs969022674 Functional Loss SNV dbSNP153 33..33 33 - - - 56833 RMVar_ID_56833 Human_SNP_ID_469996119 m1A Human chr11 - 65333895 65333895 65333895 ACCACTCACAGCTTCACTACATTCTCCACCACAGCCGCCATCTTCCCTGTTCCTCTGCCTCGGGC ACCACTCACAGCTTCACTACATTCTCCACCACGGCCGCCATCTTCCCTGTTCCTCTGCCTCGGGC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65333890..65333961 26863196 MeRIP-seq:(Medium) rs137933237 Functional Loss SNV dbSNP153 33..33 33 - - - 56834 RMVar_ID_56834 Human_SNP_ID_469996120 m1A Human chr11 - 65333895 65333895 65333895 ACCACTCACAGCTTCACTACATTCTCCACCACAGCCGCCATCTTCCCTGTTCCTCTGCCTCGGGC ACCACTCACAGCTTCACTACATTCTCCACCACCGCCGCCATCTTCCCTGTTCCTCTGCCTCGGGC T G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65333890..65333961 26863196 MeRIP-seq:(Medium) rs137933237 Functional Loss SNV dbSNP153 33..33 33 - - - 56835 RMVar_ID_56835 Human_SNP_ID_469996128 m1A Human chr11 - 65333907 65333907 65333907 GAGAAAGAAACGACCACTCACAGCTTCACTACATTCTCCACCACAGCCGCCATCTTCCCTGTTCC GAGAAAGAAACGACCACTCACAGCTTCACTACGTTCTCCACCACAGCCGCCATCTTCCCTGTTCC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65333901..65334011 26863196 MeRIP-seq:(Medium) rs146359123 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 56836 RMVar_ID_56836 Human_SNP_ID_470010540 m1A Human chr11 - 65386686 65386686 65386686 GCCTGGAATCCTGCCCCGCCGCCAAGCCCGCCACCGCCCGCACTCGGGCTCCCGCTAAGGACGCA GCCTGGAATCCTGCCCCGCCGCCAAGCCCGCCGCCGCCCGCACTCGGGCTCCCGCTAAGGACGCA T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65386679..65386789 26863196 MeRIP-seq:(Medium) rs1206675768 Functional Loss SNV dbSNP153 33..33 33 - - - 56837 RMVar_ID_56837 Human_SNP_ID_470011972 m1A Human chr11 + 65392006 65392006 65392006 GAGTTCCCAGACAGAGAGAGCATGAGGACCCCATGAGGGGCTCAGTGGCCAAGTGAGGGGAGTTA GAGTTCCCAGACAGAGAGAGCATGAGGACCCCCTGAGGGGCTCAGTGGCCAAGTGAGGGGAGTTA A C FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65392003..65392466 26863196 MeRIP-seq:(Medium) rs377619163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57264,RMVar_hsa_circ_849,RMVar_hsa_circ_101402,RMVar_hsa_circ_150632 56838 RMVar_ID_56838 Human_SNP_ID_470012169 m1A Human chr11 + 65392973 65392973 65392973 ACAAGCAAGCTGGGGATGATTTAAGGAGATTTAAGAAGGCCAAGGTGGCAGGAGCAGAGTGGGAG ACAAGCAAGCTGGGGATGATTTAAGGAGATTTGAGAAGGCCAAGGTGGCAGGAGCAGAGTGGGAG A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65392753..65393110 26863196 MeRIP-seq:(Medium) rs993250230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22643412 RMVar_hsa_circ_57264,RMVar_hsa_circ_849,RMVar_hsa_circ_101402,RMVar_hsa_circ_150632 56839 RMVar_ID_56839 Human_SNP_ID_470019108 m1A Human chr11 - 65417868 65417868 65417868 TCCTGTAGCCCCATCCTGTCACAGAGCTCACGAGACCTTCCTGTTCCCACCCTGCCACGCTGAGC TCCTGTAGCCCCATCCTGTCACAGAGCTCACGGGACCTTCCTGTTCCCACCCTGCCACGCTGAGC T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,TALAM1-001:4,L13304-001,L13705-009,TALAM1-001:5 RNACentral:URS0000D5C6F9,RNACentral:URS0000D587D6,RNACentral:URS0000D5E0AA,RNACentral:URS0000D5B1D4,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS0000D57423 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA exon,intron,exon,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65417859..65418016 26863196 MeRIP-seq:(Medium) rs1175547620 Functional Loss SNV dbSNP153 33..33 33 - - - 56840 RMVar_ID_56840 Human_SNP_ID_470020740 m1A Human chr11 + 65422932 65422932 65422932 GATGAGACGAGGGGGCGGGCTGGGGGTGCGAGAAGGAAGCTTGGCAAGGAGACTAGGTCTAGGGG GATGAGACGAGGGGGCGGGCTGGGGGTGCGAGGAGGAAGCTTGGCAAGGAGACTAGGTCTAGGGG A G NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:65422801..65423319 26863196 MeRIP-seq:(Medium) rs546142171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2584,Human_RBP_ID_228147,Human_RBP_ID_294502,Human_RBP_ID_752182,Human_RBP_ID_806825,Human_RBP_ID_868655,Human_RBP_ID_1064977,Human_RBP_ID_1078998,Human_RBP_ID_1462056,Human_RBP_ID_2275096,Human_RBP_ID_3384243,Human_RBP_ID_4187166,Human_RBP_ID_5086919,Human_RBP_ID_5138654,Human_RBP_ID_5246036,Human_RBP_ID_5549608,Human_RBP_ID_5644298,Human_RBP_ID_6085244,Human_RBP_ID_8063590,Human_RBP_ID_8177098,Human_RBP_ID_9004999,Human_RBP_ID_9414177,Human_RBP_ID_9644075,Human_RBP_ID_11671589,Human_RBP_ID_17108419,Human_RBP_ID_17184510,Human_RBP_ID_17204913,Human_RBP_ID_18932570,Human_RBP_ID_19658005,Human_RBP_ID_21966561,Human_RBP_ID_22164588,Human_RBP_ID_22380912,Human_RBP_ID_22892044,Human_RBP_ID_23154541,Human_RBP_ID_23267712,Human_RBP_ID_23513227,Human_RBP_ID_24460856,Human_RBP_ID_24557206,Human_RBP_ID_24895749,Human_RBP_ID_26776400,Human_RBP_ID_26894206,Human_RBP_ID_27154238,Human_RBP_ID_27204636,Human_RBP_ID_27836362 56841 RMVar_ID_56841 Human_SNP_ID_470020743 m1A Human chr11 - 65422940 65422940 65422940 CTGTGGTCCCCCTAGACCTAGTCTCCTTGCCAAGCTTCCTTCTCGCACCCCCAGCCCGCCCCCTC CTGTGGTCCCCCTAGACCTAGTCTCCTTGCCATGCTTCCTTCTCGCACCCCCAGCCCGCCCCCTC T A TALAM1-001,TALAM1-001:2,TALAM1-001:3,TALAM1-001:4,L13304-001,L13705-009,TALAM1-001:5,TALAM1-001:6 RNACentral:URS0000D5992E,RNACentral:URS0000D57913,RNACentral:URS0000D587D6,RNACentral:URS0000D5B1D4,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS0000D590C6,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,exon,exon,intron,intron,exon,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65422801..65423319 26863196 MeRIP-seq:(Medium) rs907601900 Functional Loss SNV dbSNP153 33..33 33 - - - 56842 RMVar_ID_56842 Human_SNP_ID_470020907 m1A Human chr11 + 65423418 65423418 65423418 ATGTAATTTTCGCTCGGCCTGGGACGGGGCCCAGGCCGGGCCCAGCCTGGTGGAGCGTCCAGGTC ATGTAATTTTCGCTCGGCCTGGGACGGGGCCCGGGCCGGGCCCAGCCTGGTGGAGCGTCCAGGTC A G NEAT1 Ensembl:ENSG00000245532 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65423371..65424137 26863196 MeRIP-seq:(Medium) rs1432383020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228150,Human_RBP_ID_752185,Human_RBP_ID_807283,Human_RBP_ID_868909,Human_RBP_ID_1079010,Human_RBP_ID_3386719,Human_RBP_ID_5086921,Human_RBP_ID_5093047,Human_RBP_ID_5169964,Human_RBP_ID_5644299,Human_RBP_ID_8176707,Human_RBP_ID_11671631,Human_RBP_ID_17110497,Human_RBP_ID_17682394,Human_RBP_ID_23513258,Human_RBP_ID_24557215,Human_RBP_ID_24913805,Human_RBP_ID_27836365 Human_miRNA_ID_3167070 56843 RMVar_ID_56843 Human_SNP_ID_470020924 m1A Human chr11 - 65423481 65423481 65423481 TTAACTCCACATCACTCCTCAGACCACCCCTCACCTCCGCCCAGGGGCCTGGCTTCGCACCCAGA TTAACTCCACATCACTCCTCAGACCACCCCTCCCCTCCGCCCAGGGGCCTGGCTTCGCACCCAGA T G L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65422801..65424183 26863196 MeRIP-seq:(Medium) rs1244054022 Functional Loss SNV dbSNP153 33..33 33 - - - 56844 RMVar_ID_56844 Human_SNP_ID_470020925 m1A Human chr11 + 65423483 65423483 65423483 TGGGTGCGAAGCCAGGCCCCTGGGCGGAGGTGAGGGGTGGTCTGAGGAGTGATGTGGAGTTAAGG TGGGTGCGAAGCCAGGCCCCTGGGCGGAGGTGCGGGGTGGTCTGAGGAGTGATGTGGAGTTAAGG A C NEAT1 Ensembl:ENSG00000245532 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65422801..65424158 26863196 MeRIP-seq:(Medium) rs1446797465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228150,Human_RBP_ID_400565,Human_RBP_ID_752186,Human_RBP_ID_807284,Human_RBP_ID_868656,Human_RBP_ID_1079012,Human_RBP_ID_1162758,Human_RBP_ID_1265250,Human_RBP_ID_1462059,Human_RBP_ID_1781168,Human_RBP_ID_2275120,Human_RBP_ID_3386723,Human_RBP_ID_5086921,Human_RBP_ID_5093047,Human_RBP_ID_5246037,Human_RBP_ID_5549619,Human_RBP_ID_5644448,Human_RBP_ID_6085270,Human_RBP_ID_8064323,Human_RBP_ID_8177038,Human_RBP_ID_8246835,Human_RBP_ID_9005012,Human_RBP_ID_9644096,Human_RBP_ID_11671634,Human_RBP_ID_17110501,Human_RBP_ID_17184520,Human_RBP_ID_17204924,Human_RBP_ID_17465542,Human_RBP_ID_17799080,Human_RBP_ID_18478507,Human_RBP_ID_18510730,Human_RBP_ID_19582515,Human_RBP_ID_21965379,Human_RBP_ID_22380918,Human_RBP_ID_22414509,Human_RBP_ID_22892068,Human_RBP_ID_23513259,Human_RBP_ID_24460868,Human_RBP_ID_24557217,Human_RBP_ID_24895767,Human_RBP_ID_26894215,Human_RBP_ID_27413999,Human_RBP_ID_27836367 Human_miRNA_ID_3150862,Human_miRNA_ID_3191504 56845 RMVar_ID_56845 Human_SNP_ID_470021037 m1A Human chr11 - 65423857 65423857 65423857 TGCACATTCACTCCCCACCCTCTCTGCAGGCAAGCAACACCGATCCGCCCCACCCCAGCCTCAGC TGCACATTCACTCCCCACCCTCTCTGCAGGCAGGCAACACCGATCCGCCCCACCCCAGCCTCAGC T C L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65423807..65424007 26863196 MeRIP-seq:(Medium) rs1289663979 Functional Loss SNV dbSNP153 33..33 33 - - - 56846 RMVar_ID_56846 Human_SNP_ID_470021423 m1A Human chr11 - 65425399 65425399 65425399 TCACTTGATAACACCCACACCCCAAACAAAACAACCCTCTGAAACAGGCTGTCTTGGCCACCAGG TCACTTGATAACACCCACACCCCAAACAAAACCACCCTCTGAAACAGGCTGTCTTGGCCACCAGG T G L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65425146..65425647 32194978 MeRIP-seq:(Medium) rs982384044 Functional Loss SNV dbSNP153 33..33 33 - - - 56847 RMVar_ID_56847 Human_SNP_ID_470021720 m1A Human chr11 - 65426699 65426699 65426699 AGATCCCATCCCCACTCAGCAGTCTGCAGACCACTTGGGATAATACCAGTTCTATCTGTGGTTAC AGATCCCATCCCCACTCAGCAGTCTGCAGACCTCTTGGGATAATACCAGTTCTATCTGTGGTTAC T A L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65426650..65426822 26863196 MeRIP-seq:(Medium) rs953475630 Functional Loss SNV dbSNP153 33..33 33 - - - 56848 RMVar_ID_56848 Human_SNP_ID_470023892 m1A Human chr11 + 65436549 65436549 65436549 CCCCAGCCTCCCTTCCCACAGAGGCCACCGTCATGGCCAGTTGCTGCAGTTTCTTTCCAGAGAAC CCCCAGCCTCCCTTCCCACAGAGGCCACCGTCCTGGCCAGTTGCTGCAGTTTCTTTCCAGAGAAC A C NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65436503..65436691 26863196 MeRIP-seq:(Medium) rs927554827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227390,Human_RBP_ID_750921,Human_RBP_ID_809267,Human_RBP_ID_1079121,Human_RBP_ID_2275701,Human_RBP_ID_3388312,Human_RBP_ID_5087141,Human_RBP_ID_5169974,Human_RBP_ID_5550965,Human_RBP_ID_8176940,Human_RBP_ID_8246926,Human_RBP_ID_8355619,Human_RBP_ID_9005246,Human_RBP_ID_9644534,Human_RBP_ID_17108582,Human_RBP_ID_17205121,Human_RBP_ID_18176173,Human_RBP_ID_18610729,Human_RBP_ID_19582810,Human_RBP_ID_22381094,Human_RBP_ID_22892532,Human_RBP_ID_23514079,Human_RBP_ID_24461484,Human_RBP_ID_24557275,Human_RBP_ID_24896352 Human_miRNA_ID_2155827,Human_miRNA_ID_2155828,Human_miRNA_ID_2155829,Human_miRNA_ID_2155830,Human_miRNA_ID_2155831,Human_miRNA_ID_2155832,Human_miRNA_ID_2155833,Human_miRNA_ID_2159389,Human_miRNA_ID_2159390,Human_miRNA_ID_2159391,Human_miRNA_ID_2159392,Human_miRNA_ID_2159393,Human_miRNA_ID_2159394,Human_miRNA_ID_2159395,Human_miRNA_ID_2393222,Human_miRNA_ID_2393223,Human_miRNA_ID_2393224,Human_miRNA_ID_2393225,Human_miRNA_ID_3158984,Human_miRNA_ID_3159183,Human_miRNA_ID_3173001 RMVar_hsa_circ_80122,RMVar_hsa_circ_102336,RMVar_hsa_circ_101409,RMVar_hsa_circ_150639,RMVar_hsa_circ_150640,RMVar_hsa_circ_116641,RMVar_hsa_circ_150641,RMVar_hsa_circ_150642 56849 RMVar_ID_56849 Human_SNP_ID_470024669 m1A Human chr11 + 65439579 65439579 65439579 ATGGTGGTGCACGTCTGTAATACCAGCTTCTCAGGAGGCTGAGGCACGAGGATCACTTGAACCCA ATGGTGGTGCACGTCTGTAATACCAGCTTCTCGGGAGGCTGAGGCACGAGGATCACTTGAACCCA A G NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65439529..65439663 26863196 MeRIP-seq:(Medium) rs1254376644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5093128,Human_RBP_ID_8246927,Human_RBP_ID_11672878 56850 RMVar_ID_56850 Human_SNP_ID_470024918 m1A Human chr11 - 65440601 65440601 65440601 TGACCTCGTGATCCACCCACCTTGGCCTCCCAATCTTATTTGCTTTACAAGTCCTGCTTCAGGGT TGACCTCGTGATCCACCCACCTTGGCCTCCCAGTCTTATTTGCTTTACAAGTCCTGCTTCAGGGT T C L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65440551..65440650 26863196 MeRIP-seq:(Medium) rs1432840001 Functional Loss SNV dbSNP153 33..33 33 - - - 56851 RMVar_ID_56851 Human_SNP_ID_470025012 m1A Human chr11 + 65440921 65440920 65440921 AACTTCTTCTGCTTGGACTTAAGGGCATCATCAGGCAGGTTTTGGGTAGGATAGCAGGGGAGGCA AACTTCTTCTGCTTGGACTTAAGGGCATCATC_GGCAGGTTTTGGGTAGGATAGCAGGGGAGGCA CA C NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65440871..65441040 26863196 MeRIP-seq:(Medium) rs1565636459 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2275882,Human_RBP_ID_5093137,Human_RBP_ID_5549841,Human_RBP_ID_6085660,Human_RBP_ID_8247297,Human_RBP_ID_9644676,Human_RBP_ID_11672989,Human_RBP_ID_17184631,Human_RBP_ID_22381155,Human_RBP_ID_22892666,Human_RBP_ID_23154585,Human_RBP_ID_23514279,Human_RBP_ID_24461628,Human_RBP_ID_24896705 56852 RMVar_ID_56852 Human_SNP_ID_470025594 m1A Human chr11 + 65443652 65443652 65443652 AGCATTTTGTGGTTACGAATTCTACAGTCACAAATATCTTTGGGCAAATCCCCTTCTATACCTCA AGCATTTTGTGGTTACGAATTCTACAGTCACAGATATCTTTGGGCAAATCCCCTTCTATACCTCA A G NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65443601..65443744 26863196 MeRIP-seq:(Medium) rs148976148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1781419,Human_RBP_ID_2275970,Human_RBP_ID_3378023,Human_RBP_ID_5549868,Human_RBP_ID_8062068,Human_RBP_ID_8247016,Human_RBP_ID_9005331,Human_RBP_ID_11673245,Human_RBP_ID_17108655,Human_RBP_ID_17465594,Human_RBP_ID_17799114,Human_RBP_ID_18478614,Human_RBP_ID_18610766,Human_RBP_ID_19582927,Human_RBP_ID_22381188,Human_RBP_ID_22695646,Human_RBP_ID_23514401,Human_RBP_ID_24404058,Human_RBP_ID_24461691,Human_RBP_ID_24896802 Human_miRNA_ID_2364253,Human_miRNA_ID_3067192,Human_miRNA_ID_3171142,Human_miRNA_ID_3213202 RMVar_hsa_circ_113760,RMVar_hsa_circ_150643 56853 RMVar_ID_56853 Human_SNP_ID_470025732 m1A Human chr11 + 65444202 65444202 65444202 GGGGCAAAGGCAGTTGGCCCAACACATTCCCCACCCCTTTGAGAGGTCTGAGGCCTGCAGACCTG GGGGCAAAGGCAGTTGGCCCAACACATTCCCCTCCCCTTTGAGAGGTCTGAGGCCTGCAGACCTG A T NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65444151..65444250 26863196 MeRIP-seq:(Medium) rs777925294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2591,Human_RBP_ID_868686,Human_RBP_ID_2275999,Human_RBP_ID_3384317,Human_RBP_ID_5093154,Human_RBP_ID_5246051,Human_RBP_ID_5282123,Human_RBP_ID_5549873,Human_RBP_ID_5643800,Human_RBP_ID_8062071,Human_RBP_ID_8176677,Human_RBP_ID_8355697,Human_RBP_ID_8946085,Human_RBP_ID_9005340,Human_RBP_ID_11673302,Human_RBP_ID_17205145,Human_RBP_ID_17234978,Human_RBP_ID_18416918,Human_RBP_ID_18477944,Human_RBP_ID_19582940,Human_RBP_ID_22164829,Human_RBP_ID_22381195,Human_RBP_ID_22892771,Human_RBP_ID_23113119,Human_RBP_ID_23514427,Human_RBP_ID_24896802,Human_RBP_ID_26894520 Human_miRNA_ID_3192592 56854 RMVar_ID_56854 Human_SNP_ID_470025794 m1A Human chr11 + 65444325 65444322 65444326 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAAGAGAGAAGTTGTGGAGAAATGGGGGGCTGAT GTGTGTGTGTGTGTGTGTGTGTGTGTGTGT____GAGAGAAGTTGTGGAGAAATGGGGGGCTGAT TAAAA T NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:65444276..65444325;chr11:65444276..65444375;chr11:65444276..65444350 26863196 MeRIP-seq:(Medium) rs1260699024 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_2592,Human_RBP_ID_400647,Human_RBP_ID_1080420,Human_RBP_ID_2276006,Human_RBP_ID_3384318,Human_RBP_ID_4187033,Human_RBP_ID_5138657,Human_RBP_ID_5168487,Human_RBP_ID_5282125,Human_RBP_ID_5521159,Human_RBP_ID_5549874,Human_RBP_ID_5643803,Human_RBP_ID_8063622,Human_RBP_ID_8946086,Human_RBP_ID_11673310,Human_RBP_ID_17108665,Human_RBP_ID_17184656,Human_RBP_ID_17205274,Human_RBP_ID_17234165,Human_RBP_ID_18159852,Human_RBP_ID_18456479,Human_RBP_ID_19658755,Human_RBP_ID_21966583,Human_RBP_ID_22414655,Human_RBP_ID_22705622,Human_RBP_ID_22892774,Human_RBP_ID_23113022,Human_RBP_ID_23514427,Human_RBP_ID_24461713,Human_RBP_ID_24896854,Human_RBP_ID_26894523 Human_miRNA_ID_3216167 56855 RMVar_ID_56855 Human_SNP_ID_470025946 m1A Human chr11 - 65444739 65444739 65444739 TTCTCCTGTCACTTGACTCTAACCTGGAGTCCAAGTCACCAGGGCCCCAGGACCCAAAGGTACAC TTCTCCTGTCACTTGACTCTAACCTGGAGTCCCAGTCACCAGGGCCCCAGGACCCAAAGGTACAC T G L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65444689..65444998 26863196 MeRIP-seq:(Medium) rs887350770 Functional Loss SNV dbSNP153 33..33 33 - - - 56856 RMVar_ID_56856 Human_SNP_ID_470041311 m1A Human chr11 - 65499075 65499067 65499075 CGGTTTCCTCAAGCTCCGCCTGCCCCCTCAGCAGAAGCCCCTGCGCTGGCTGCCTCAATGCCTAC CGGTTTCCTCAAGCTCCGCCTGCCCCCTCAGC________CTGCGCTGGCTGCCTCAATGCCTAC GGGGCTTCT G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4,TALAM1-001:5 RNACentral:URS00008BD2DE,RNACentral:URS00008B3D99,RNACentral:URS0000D5C36E,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA intron,intron,exon,intron,intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65499051..65499075 26863196 MeRIP-seq:(Medium) rs779004594 Functional Loss DEL dbSNP153 33..40 33 - - - 56857 RMVar_ID_56857 Human_SNP_ID_470041332 m1A Human chr11 - 65499075 65499075 65499075 CGGTTTCCTCAAGCTCCGCCTGCCCCCTCAGCAGAAGCCCCTGCGCTGGCTGCCTCAATGCCTAC CGGTTTCCTCAAGCTCCGCCTGCCCCCTCAGCGGAAGCCCCTGCGCTGGCTGCCTCAATGCCTAC T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4,TALAM1-001:5 RNACentral:URS00008BD2DE,RNACentral:URS00008B3D99,RNACentral:URS0000D5C36E,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA intron,intron,exon,intron,intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65499051..65499075 26863196 MeRIP-seq:(Medium) rs1355065655 Functional Loss SNV dbSNP153 33..33 33 - - - 56858 RMVar_ID_56858 Human_SNP_ID_470041382 m1A Human chr11 + 65499114 65499114 65499114 GGGGCAGGCGGAGCTTGAGGAAACCGCAGATAAGTTTTTTTCTCTTTGAAAGATAGAGATTAATA GGGGCAGGCGGAGCTTGAGGAAACCGCAGATACGTTTTTTTCTCTTTGAAAGATAGAGATTAATA A C MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499051..65499150 32194978 MeRIP-seq:(Medium) rs766966793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228201,Human_RBP_ID_274843,Human_RBP_ID_752229,Human_RBP_ID_807129,Human_RBP_ID_1126450,Human_RBP_ID_1162901,Human_RBP_ID_1459102,Human_RBP_ID_2276077,Human_RBP_ID_3378039,Human_RBP_ID_4193144,Human_RBP_ID_5551383,Human_RBP_ID_6085827,Human_RBP_ID_8355733,Human_RBP_ID_9005358,Human_RBP_ID_9644798,Human_RBP_ID_11673528,Human_RBP_ID_17062244,Human_RBP_ID_17184682,Human_RBP_ID_18416923,Human_RBP_ID_18610790,Human_RBP_ID_19028318,Human_RBP_ID_19658845,Human_RBP_ID_22032794,Human_RBP_ID_22164846,Human_RBP_ID_22381211,Human_RBP_ID_22491572,Human_RBP_ID_22791553,Human_RBP_ID_22892800,Human_RBP_ID_23154620,Human_RBP_ID_23514555,Human_RBP_ID_24404073,Human_RBP_ID_24461744,Human_RBP_ID_24896919,Human_RBP_ID_26605322,Human_RBP_ID_26894545,Human_RBP_ID_27204926 56859 RMVar_ID_56859 Human_SNP_ID_470041383 m1A Human chr11 + 65499114 65499114 65499114 GGGGCAGGCGGAGCTTGAGGAAACCGCAGATAAGTTTTTTTCTCTTTGAAAGATAGAGATTAATA GGGGCAGGCGGAGCTTGAGGAAACCGCAGATAGGTTTTTTTCTCTTTGAAAGATAGAGATTAATA A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499051..65499150 32194978 MeRIP-seq:(Medium) rs766966793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228201,Human_RBP_ID_274843,Human_RBP_ID_752229,Human_RBP_ID_807129,Human_RBP_ID_1126450,Human_RBP_ID_1162901,Human_RBP_ID_1459102,Human_RBP_ID_2276077,Human_RBP_ID_3378039,Human_RBP_ID_4193144,Human_RBP_ID_5551383,Human_RBP_ID_6085827,Human_RBP_ID_8355733,Human_RBP_ID_9005358,Human_RBP_ID_9644798,Human_RBP_ID_11673528,Human_RBP_ID_17062244,Human_RBP_ID_17184682,Human_RBP_ID_18416923,Human_RBP_ID_18610790,Human_RBP_ID_19028318,Human_RBP_ID_19658845,Human_RBP_ID_22032794,Human_RBP_ID_22164846,Human_RBP_ID_22381211,Human_RBP_ID_22491572,Human_RBP_ID_22791553,Human_RBP_ID_22892800,Human_RBP_ID_23154620,Human_RBP_ID_23514555,Human_RBP_ID_24404073,Human_RBP_ID_24461744,Human_RBP_ID_24896919,Human_RBP_ID_26605322,Human_RBP_ID_26894545,Human_RBP_ID_27204926 56860 RMVar_ID_56860 Human_SNP_ID_470041384 m1A Human chr11 + 65499114 65499114 65499114 GGGGCAGGCGGAGCTTGAGGAAACCGCAGATAAGTTTTTTTCTCTTTGAAAGATAGAGATTAATA GGGGCAGGCGGAGCTTGAGGAAACCGCAGATATGTTTTTTTCTCTTTGAAAGATAGAGATTAATA A T MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499051..65499150 32194978 MeRIP-seq:(Medium) rs766966793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228201,Human_RBP_ID_274843,Human_RBP_ID_752229,Human_RBP_ID_807129,Human_RBP_ID_1126450,Human_RBP_ID_1162901,Human_RBP_ID_1459102,Human_RBP_ID_2276077,Human_RBP_ID_3378039,Human_RBP_ID_4193144,Human_RBP_ID_5551383,Human_RBP_ID_6085827,Human_RBP_ID_8355733,Human_RBP_ID_9005358,Human_RBP_ID_9644798,Human_RBP_ID_11673528,Human_RBP_ID_17062244,Human_RBP_ID_17184682,Human_RBP_ID_18416923,Human_RBP_ID_18610790,Human_RBP_ID_19028318,Human_RBP_ID_19658845,Human_RBP_ID_22032794,Human_RBP_ID_22164846,Human_RBP_ID_22381211,Human_RBP_ID_22491572,Human_RBP_ID_22791553,Human_RBP_ID_22892800,Human_RBP_ID_23154620,Human_RBP_ID_23514555,Human_RBP_ID_24404073,Human_RBP_ID_24461744,Human_RBP_ID_24896919,Human_RBP_ID_26605322,Human_RBP_ID_26894545,Human_RBP_ID_27204926 56861 RMVar_ID_56861 Human_SNP_ID_470041517 m1A Human chr11 + 65499258 65499256 65499259 AGATTTTAAGAGAAAATATGAAGACTTAGAAGAGTAGCATGAGGAAGGAAAAGATAAAAGGTTTC AGATTTTAAGAGAAAATATGAAGACTTAGAA___TAGCATGAGGAAGGAAAAGATAAAAGGTTTC AGAG A MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499176..65499575 32194978 MeRIP-seq:(Medium) rs777762933 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1079176,Human_RBP_ID_1781440,Human_RBP_ID_2276077,Human_RBP_ID_3378043,Human_RBP_ID_4171551,Human_RBP_ID_5169995,Human_RBP_ID_5549896,Human_RBP_ID_5644493,Human_RBP_ID_6085833,Human_RBP_ID_8246929,Human_RBP_ID_8355734,Human_RBP_ID_9005358,Human_RBP_ID_9644799,Human_RBP_ID_11673531,Human_RBP_ID_17184682,Human_RBP_ID_17465604,Human_RBP_ID_18176178,Human_RBP_ID_18251561,Human_RBP_ID_18433013,Human_RBP_ID_18610793,Human_RBP_ID_22164846,Human_RBP_ID_22491573,Human_RBP_ID_22791557,Human_RBP_ID_22892800,Human_RBP_ID_23154621,Human_RBP_ID_23514560,Human_RBP_ID_24404078,Human_RBP_ID_24461750,Human_RBP_ID_24542406,Human_RBP_ID_24896919,Human_RBP_ID_26894545,Human_RBP_ID_27414249 Human_Splice_Rec_1258551,Human_Splice_Rec_1258553 Human_miRNA_ID_3208850 RMVar_hsa_circ_150645 56862 RMVar_ID_56862 Human_SNP_ID_470041521 m1A Human chr11 + 65499258 65499258 65499258 AGATTTTAAGAGAAAATATGAAGACTTAGAAGAGTAGCATGAGGAAGGAAAAGATAAAAGGTTTC AGATTTTAAGAGAAAATATGAAGACTTAGAAGGGTAGCATGAGGAAGGAAAAGATAAAAGGTTTC A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499176..65499575 32194978 MeRIP-seq:(Medium) rs771918330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1079176,Human_RBP_ID_1781440,Human_RBP_ID_2276077,Human_RBP_ID_3378043,Human_RBP_ID_4171551,Human_RBP_ID_5169995,Human_RBP_ID_5549896,Human_RBP_ID_5644493,Human_RBP_ID_6085833,Human_RBP_ID_8246929,Human_RBP_ID_8355734,Human_RBP_ID_9005358,Human_RBP_ID_9644799,Human_RBP_ID_11673531,Human_RBP_ID_17184682,Human_RBP_ID_17465604,Human_RBP_ID_18176178,Human_RBP_ID_18251561,Human_RBP_ID_18433013,Human_RBP_ID_18610793,Human_RBP_ID_22164846,Human_RBP_ID_22491573,Human_RBP_ID_22791557,Human_RBP_ID_22892800,Human_RBP_ID_23154621,Human_RBP_ID_23514560,Human_RBP_ID_24404078,Human_RBP_ID_24461750,Human_RBP_ID_24542406,Human_RBP_ID_24896919,Human_RBP_ID_26894545,Human_RBP_ID_27414249 Human_Splice_Rec_1258551,Human_Splice_Rec_1258553 Human_miRNA_ID_3208850 RMVar_hsa_circ_150645 56863 RMVar_ID_56863 Human_SNP_ID_470041845 m1A Human chr11 + 65499675 65499674 65499676 AGATAGAAGTTTGAAGTGGAAAACTGGAAGACAGAAGTACGGGAAGGCGAAGAAAAGAATAGAGA AGATAGAAGTTTGAAGTGGAAAACTGGAAGAC__AAGTACGGGAAGGCGAAGAAAAGAATAGAGA CAG C MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65499574..65499797;chr11:65499576..65499815;chr11:65499051..65499967;chr11:65499051..65499980;chr11:65499051..65499964 26863196 MeRIP-seq:(Medium) rs780027619 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_228202,Human_RBP_ID_294154,Human_RBP_ID_807130,Human_RBP_ID_867732,Human_RBP_ID_987957,Human_RBP_ID_1079187,Human_RBP_ID_1461984,Human_RBP_ID_1781440,Human_RBP_ID_2276078,Human_RBP_ID_4171573,Human_RBP_ID_5169354,Human_RBP_ID_5549902,Human_RBP_ID_5644488,Human_RBP_ID_6085847,Human_RBP_ID_8177124,Human_RBP_ID_8246510,Human_RBP_ID_9005358,Human_RBP_ID_9414199,Human_RBP_ID_9644804,Human_RBP_ID_10482279,Human_RBP_ID_11673531,Human_RBP_ID_17062249,Human_RBP_ID_17067102,Human_RBP_ID_17184682,Human_RBP_ID_17668713,Human_RBP_ID_17799127,Human_RBP_ID_18525935,Human_RBP_ID_22000808,Human_RBP_ID_22164851,Human_RBP_ID_22352924,Human_RBP_ID_22522040,Human_RBP_ID_22791567,Human_RBP_ID_22892822,Human_RBP_ID_23117871,Human_RBP_ID_23154631,Human_RBP_ID_23514590,Human_RBP_ID_24461763,Human_RBP_ID_24542413,Human_RBP_ID_24896933,Human_RBP_ID_26318677,Human_RBP_ID_26894549,Human_RBP_ID_27414251,Human_RBP_ID_27618912,Human_RBP_ID_27803594 Human_Splice_Rec_1258552 RMVar_hsa_circ_150649,RMVar_hsa_circ_150648,RMVar_hsa_circ_379034 56864 RMVar_ID_56864 Human_SNP_ID_470041848 m1A Human chr11 + 65499675 65499675 65499675 AGATAGAAGTTTGAAGTGGAAAACTGGAAGACAGAAGTACGGGAAGGCGAAGAAAAGAATAGAGA AGATAGAAGTTTGAAGTGGAAAACTGGAAGACGGAAGTACGGGAAGGCGAAGAAAAGAATAGAGA A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65499574..65499797;chr11:65499576..65499815;chr11:65499051..65499967;chr11:65499051..65499980;chr11:65499051..65499964 26863196 MeRIP-seq:(Medium) rs1387682811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228202,Human_RBP_ID_294154,Human_RBP_ID_807130,Human_RBP_ID_867732,Human_RBP_ID_987957,Human_RBP_ID_1079187,Human_RBP_ID_1461984,Human_RBP_ID_1781440,Human_RBP_ID_2276078,Human_RBP_ID_4171573,Human_RBP_ID_5169354,Human_RBP_ID_5549902,Human_RBP_ID_5644488,Human_RBP_ID_6085847,Human_RBP_ID_8177124,Human_RBP_ID_8246510,Human_RBP_ID_9005358,Human_RBP_ID_9414199,Human_RBP_ID_9644804,Human_RBP_ID_10482279,Human_RBP_ID_11673531,Human_RBP_ID_17062249,Human_RBP_ID_17067102,Human_RBP_ID_17184682,Human_RBP_ID_17668713,Human_RBP_ID_17799127,Human_RBP_ID_18525935,Human_RBP_ID_22000808,Human_RBP_ID_22164851,Human_RBP_ID_22352924,Human_RBP_ID_22522040,Human_RBP_ID_22791567,Human_RBP_ID_22892822,Human_RBP_ID_23117871,Human_RBP_ID_23154631,Human_RBP_ID_23514590,Human_RBP_ID_24461763,Human_RBP_ID_24542413,Human_RBP_ID_24896933,Human_RBP_ID_26318677,Human_RBP_ID_26894549,Human_RBP_ID_27414251,Human_RBP_ID_27618912,Human_RBP_ID_27803594 Human_Splice_Rec_1258552 RMVar_hsa_circ_150649,RMVar_hsa_circ_150648,RMVar_hsa_circ_379034 56865 RMVar_ID_56865 Human_SNP_ID_470041861 m1A Human chr11 + 65499696 65499696 65499696 AACTGGAAGACAGAAGTACGGGAAGGCGAAGAAAAGAATAGAGAAGATAGGGAAATTAGAAGATA AACTGGAAGACAGAAGTACGGGAAGGCGAAGAGAAGAATAGAGAAGATAGGGAAATTAGAAGATA A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:65499598..65499765 26863196 MeRIP-seq:(Medium) rs1438355659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228202,Human_RBP_ID_400660,Human_RBP_ID_751108,Human_RBP_ID_807130,Human_RBP_ID_867733,Human_RBP_ID_1461986,Human_RBP_ID_1781446,Human_RBP_ID_2276078,Human_RBP_ID_3388396,Human_RBP_ID_4171573,Human_RBP_ID_5549902,Human_RBP_ID_5644488,Human_RBP_ID_6085847,Human_RBP_ID_8177124,Human_RBP_ID_8246510,Human_RBP_ID_9005358,Human_RBP_ID_9414199,Human_RBP_ID_9644804,Human_RBP_ID_11673532,Human_RBP_ID_17184682,Human_RBP_ID_17668713,Human_RBP_ID_18176185,Human_RBP_ID_18525935,Human_RBP_ID_22352927,Human_RBP_ID_22522043,Human_RBP_ID_22892822,Human_RBP_ID_23117871,Human_RBP_ID_24542416,Human_RBP_ID_24896942,Human_RBP_ID_26318679,Human_RBP_ID_26894549,Human_RBP_ID_27414251,Human_RBP_ID_27803597 Human_Splice_Rec_1258552,Human_Splice_Rec_1258554 Human_miRNA_ID_3216168 RMVar_hsa_circ_150650,RMVar_hsa_circ_150649,RMVar_hsa_circ_150651 56866 RMVar_ID_56866 Human_SNP_ID_470042193 m1A Human chr11 + 65500183 65500183 65500183 TCACATCAAAAAGCTACTAAAAGGACTGGTGTAATTTAAAAAAAACTAAGGCAGAAGGCTTTTGG TCACATCAAAAAGCTACTAAAAGGACTGGTGTGATTTAAAAAAAACTAAGGCAGAAGGCTTTTGG A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65500133..65500266 26863196 MeRIP-seq:(Medium) rs1445383442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1080445,Human_RBP_ID_1126604,Human_RBP_ID_1459123,Human_RBP_ID_1781446,Human_RBP_ID_2276078,Human_RBP_ID_3378050,Human_RBP_ID_5549909,Human_RBP_ID_6085872,Human_RBP_ID_8064561,Human_RBP_ID_8355751,Human_RBP_ID_9005358,Human_RBP_ID_9644816,Human_RBP_ID_10482284,Human_RBP_ID_11673598,Human_RBP_ID_17062253,Human_RBP_ID_17184691,Human_RBP_ID_17799133,Human_RBP_ID_18176489,Human_RBP_ID_19582980,Human_RBP_ID_22032803,Human_RBP_ID_22164856,Human_RBP_ID_22381237,Human_RBP_ID_22521756,Human_RBP_ID_22892857,Human_RBP_ID_23267208,Human_RBP_ID_23514638,Human_RBP_ID_24404092,Human_RBP_ID_24461772,Human_RBP_ID_24896971,Human_RBP_ID_26320138,Human_RBP_ID_26894554,Human_RBP_ID_27618921,Human_RBP_ID_27804641 RMVar_hsa_circ_150655,RMVar_hsa_circ_150650,RMVar_hsa_circ_150649,RMVar_hsa_circ_150651,RMVar_hsa_circ_150656 56867 RMVar_ID_56867 Human_SNP_ID_470042490 m1A Human chr11 + 65500653 65500653 65500653 GGAAGGAGCGAGTGCAATTTGGTGATGAAGGTAGCAGGCGGCTTGGCTTGGCAACCACACGGAGG GGAAGGAGCGAGTGCAATTTGGTGATGAAGGTTGCAGGCGGCTTGGCTTGGCAACCACACGGAGG A T MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65500410..65500878 26863196 MeRIP-seq:(Medium) rs565447999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228233,Human_RBP_ID_294161,Human_RBP_ID_400681,Human_RBP_ID_752233,Human_RBP_ID_806865,Human_RBP_ID_869157,Human_RBP_ID_1080454,Human_RBP_ID_1126455,Human_RBP_ID_1354841,Human_RBP_ID_1462343,Human_RBP_ID_2276078,Human_RBP_ID_3388400,Human_RBP_ID_4171636,Human_RBP_ID_5086995,Human_RBP_ID_5169357,Human_RBP_ID_5549916,Human_RBP_ID_5644498,Human_RBP_ID_6085895,Human_RBP_ID_8064634,Human_RBP_ID_8177126,Human_RBP_ID_8247290,Human_RBP_ID_9005372,Human_RBP_ID_9644823,Human_RBP_ID_11673610,Human_RBP_ID_17184695,Human_RBP_ID_19028159,Human_RBP_ID_19658908,Human_RBP_ID_22164860,Human_RBP_ID_22352940,Human_RBP_ID_22381242,Human_RBP_ID_22522130,Human_RBP_ID_22791602,Human_RBP_ID_22892872,Human_RBP_ID_23117891,Human_RBP_ID_23267212,Human_RBP_ID_23514666,Human_RBP_ID_24404101,Human_RBP_ID_24461795,Human_RBP_ID_24542514,Human_RBP_ID_24896971,Human_RBP_ID_26318716,Human_RBP_ID_26894556,Human_RBP_ID_27414263,Human_RBP_ID_27618922,Human_RBP_ID_27803614 Human_miRNA_ID_3209569 RMVar_hsa_circ_150649,RMVar_hsa_circ_150662 56868 RMVar_ID_56868 Human_SNP_ID_470043111 m1A Human chr11 - 65501572 65501572 65501572 GTACTATAGCATCTGTGGAAAATCTTAGAAAAAAACATTTTCTCCCCCACCCTCTCTCTTCCCTG GTACTATAGCATCTGTGGAAAATCTTAGAAAACAACATTTTCTCCCCCACCCTCTCTCTTCCCTG T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4,TALAM1-001:5 RNACentral:URS00008B3291,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,exon,intron,intron,intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65501417..65501787 26863196 MeRIP-seq:(Medium) rs1320042300 Functional Loss SNV dbSNP153 33..33 33 - - - 56869 RMVar_ID_56869 Human_SNP_ID_470043149 m1A Human chr11 - 65501632 65501632 65501632 TGAAGGTGTTCGTGCCAACAGCACAGCGGTACACTCCTTCTCTAACCCAGTTTGTCAATAGTACT TGAAGGTGTTCGTGCCAACAGCACAGCGGTACCCTCCTTCTCTAACCCAGTTTGTCAATAGTACT T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4,TALAM1-001:5 RNACentral:URS00008B3291,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,exon,intron,intron,intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65501518..65501787 26863196 MeRIP-seq:(Medium) rs1340297567 Functional Loss SNV dbSNP153 33..33 33 - - - 56870 RMVar_ID_56870 Human_SNP_ID_470043264 m1A Human chr11 + 65501852 65501852 65501852 CTTCTTAAAAGTTTTATTAAAGGGGAGGGGCAAATATTGGCAATTAGTTGGCAGTGGCCTGTTAC CTTCTTAAAAGTTTTATTAAAGGGGAGGGGCAGATATTGGCAATTAGTTGGCAGTGGCCTGTTAC A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65501266..65501997;chr11:65501226..65502004;chr11:65501476..65501974 26863196 MeRIP-seq:(Medium) rs1360119798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400720,Human_RBP_ID_751111,Human_RBP_ID_806872,Human_RBP_ID_987972,Human_RBP_ID_1079242,Human_RBP_ID_1126613,Human_RBP_ID_2276079,Human_RBP_ID_3378070,Human_RBP_ID_4171699,Human_RBP_ID_5087000,Human_RBP_ID_5549941,Human_RBP_ID_6085918,Human_RBP_ID_8176874,Human_RBP_ID_8246937,Human_RBP_ID_8355805,Human_RBP_ID_9005397,Human_RBP_ID_9644832,Human_RBP_ID_11673670,Human_RBP_ID_17108704,Human_RBP_ID_17184695,Human_RBP_ID_17799149,Human_RBP_ID_18251583,Human_RBP_ID_18610876,Human_RBP_ID_18932587,Human_RBP_ID_19658952,Human_RBP_ID_22381250,Human_RBP_ID_22791651,Human_RBP_ID_22892928,Human_RBP_ID_23124657,Human_RBP_ID_23514798,Human_RBP_ID_24404149,Human_RBP_ID_24461804,Human_RBP_ID_24896971,Human_RBP_ID_26894566,Human_RBP_ID_27414293,Human_RBP_ID_27618935 RMVar_hsa_circ_150669,RMVar_hsa_circ_150668,RMVar_hsa_circ_150670 56871 RMVar_ID_56871 Human_SNP_ID_470043473 m1A Human chr11 + 65502221 65502221 65502221 GGTTGGTCTGGCCTACTGGGCTGACATTAACTACAATTATGGGAAATGCAAAAGTTGTTTGGATA GGTTGGTCTGGCCTACTGGGCTGACATTAACTGCAATTATGGGAAATGCAAAAGTTGTTTGGATA A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65502069..65502336 26863196 MeRIP-seq:(Medium) rs746154727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227436,Human_RBP_ID_274631,Human_RBP_ID_400734,Human_RBP_ID_751114,Human_RBP_ID_806873,Human_RBP_ID_1063908,Human_RBP_ID_1079254,Human_RBP_ID_1162938,Human_RBP_ID_1265353,Human_RBP_ID_1459177,Human_RBP_ID_1781471,Human_RBP_ID_2276079,Human_RBP_ID_3378072,Human_RBP_ID_4171724,Human_RBP_ID_5087002,Human_RBP_ID_5093191,Human_RBP_ID_5549943,Human_RBP_ID_6086025,Human_RBP_ID_8062083,Human_RBP_ID_8246516,Human_RBP_ID_8355808,Human_RBP_ID_9005397,Human_RBP_ID_9644837,Human_RBP_ID_10482298,Human_RBP_ID_11673670,Human_RBP_ID_16987128,Human_RBP_ID_17062278,Human_RBP_ID_17108710,Human_RBP_ID_17184730,Human_RBP_ID_17349134,Human_RBP_ID_17799154,Human_RBP_ID_18176223,Human_RBP_ID_18251588,Human_RBP_ID_18610885,Human_RBP_ID_19583021,Human_RBP_ID_22164879,Human_RBP_ID_22381261,Human_RBP_ID_22491594,Human_RBP_ID_22791662,Human_RBP_ID_22892933,Human_RBP_ID_23267214,Human_RBP_ID_23514857,Human_RBP_ID_24404164,Human_RBP_ID_24461804,Human_RBP_ID_24896971,Human_RBP_ID_27414301,Human_RBP_ID_27618935 RMVar_hsa_circ_150669,RMVar_hsa_circ_150670 56872 RMVar_ID_56872 Human_SNP_ID_470043727 m1A Human chr11 + 65502703 65502703 65502703 AGCCTGGCAGTATGATGGCCTAGATGCAGAGAAAACAGCTCCTTGGTGAATTGATAAGTAAAGGC AGCCTGGCAGTATGATGGCCTAGATGCAGAGAGAACAGCTCCTTGGTGAATTGATAAGTAAAGGC A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65502585..65502859 26863196 MeRIP-seq:(Medium) rs775812432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400750,Human_RBP_ID_806774,Human_RBP_ID_1080530,Human_RBP_ID_1162951,Human_RBP_ID_1354857,Human_RBP_ID_1459193,Human_RBP_ID_1781471,Human_RBP_ID_2276079,Human_RBP_ID_3378077,Human_RBP_ID_4193245,Human_RBP_ID_5087005,Human_RBP_ID_5549950,Human_RBP_ID_5644475,Human_RBP_ID_6086065,Human_RBP_ID_8355827,Human_RBP_ID_9005397,Human_RBP_ID_9644837,Human_RBP_ID_11673766,Human_RBP_ID_17108714,Human_RBP_ID_17184731,Human_RBP_ID_17465687,Human_RBP_ID_18176233,Human_RBP_ID_18251594,Human_RBP_ID_18610900,Human_RBP_ID_19698325,Human_RBP_ID_22164887,Human_RBP_ID_22381269,Human_RBP_ID_22892933,Human_RBP_ID_23268009,Human_RBP_ID_23514871,Human_RBP_ID_24461804,Human_RBP_ID_24896971,Human_RBP_ID_26405846,Human_RBP_ID_27618945 Human_Splice_Rec_1258560 Human_miRNA_ID_2292162,Human_miRNA_ID_2357505,Human_miRNA_ID_3059946,Human_miRNA_ID_3166872,Human_miRNA_ID_3170758,Human_miRNA_ID_3212778 RMVar_hsa_circ_150673,RMVar_hsa_circ_377612,RMVar_hsa_circ_150674 56873 RMVar_ID_56873 Human_SNP_ID_470043908 m1A Human chr11 + 65503020 65503020 65503020 AGCGAAAAGAAATGAAAATGTTACACTACATTAATCCTGGAATAAAAGAAGCCGAAATAAATGAG AGCGAAAAGAAATGAAAATGTTACACTACATTGATCCTGGAATAAAAGAAGCCGAAATAAATGAG A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65502970..65503112 26863196 MeRIP-seq:(Medium) rs1324602980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400757,Human_RBP_ID_1079264,Human_RBP_ID_1126616,Human_RBP_ID_1162963,Human_RBP_ID_1265362,Human_RBP_ID_1354858,Human_RBP_ID_1459202,Human_RBP_ID_1781471,Human_RBP_ID_2276079,Human_RBP_ID_3378080,Human_RBP_ID_4171765,Human_RBP_ID_5246080,Human_RBP_ID_5549953,Human_RBP_ID_6086094,Human_RBP_ID_8064933,Human_RBP_ID_8355839,Human_RBP_ID_9005397,Human_RBP_ID_9644837,Human_RBP_ID_10482304,Human_RBP_ID_11673829,Human_RBP_ID_16987138,Human_RBP_ID_17062291,Human_RBP_ID_17184731,Human_RBP_ID_17349137,Human_RBP_ID_17465694,Human_RBP_ID_17799171,Human_RBP_ID_18205868,Human_RBP_ID_18251599,Human_RBP_ID_18525956,Human_RBP_ID_18610912,Human_RBP_ID_19583039,Human_RBP_ID_22164893,Human_RBP_ID_22381270,Human_RBP_ID_22522138,Human_RBP_ID_22791682,Human_RBP_ID_22892969,Human_RBP_ID_23268011,Human_RBP_ID_23514928,Human_RBP_ID_24404199,Human_RBP_ID_24461804,Human_RBP_ID_24897068,Human_RBP_ID_26405857,Human_RBP_ID_26605369,Human_RBP_ID_26747688,Human_RBP_ID_26894577,Human_RBP_ID_27414323,Human_RBP_ID_27618953 RMVar_hsa_circ_150673,RMVar_hsa_circ_377612,RMVar_hsa_circ_150677 56874 RMVar_ID_56874 Human_SNP_ID_470043924 m1A Human chr11 + 65503047 65503047 65503047 ACATTAATCCTGGAATAAAAGAAGCCGAAATAAATGAGAGATGAGTTGGGATCAAGTGGATTGAG ACATTAATCCTGGAATAAAAGAAGCCGAAATAGATGAGAGATGAGTTGGGATCAAGTGGATTGAG A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65502996..65503074 26863196 MeRIP-seq:(Medium) rs756416948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400758,Human_RBP_ID_1126616,Human_RBP_ID_1354859,Human_RBP_ID_1459204,Human_RBP_ID_1781471,Human_RBP_ID_2276079,Human_RBP_ID_3378080,Human_RBP_ID_4171765,Human_RBP_ID_5246080,Human_RBP_ID_5549953,Human_RBP_ID_6086094,Human_RBP_ID_8355839,Human_RBP_ID_9005397,Human_RBP_ID_9644837,Human_RBP_ID_10482304,Human_RBP_ID_11673829,Human_RBP_ID_17062291,Human_RBP_ID_17108718,Human_RBP_ID_17184731,Human_RBP_ID_17799172,Human_RBP_ID_18176235,Human_RBP_ID_18251600,Human_RBP_ID_18525957,Human_RBP_ID_18610912,Human_RBP_ID_19583039,Human_RBP_ID_22381270,Human_RBP_ID_22791683,Human_RBP_ID_22892969,Human_RBP_ID_23267215,Human_RBP_ID_23514928,Human_RBP_ID_24404200,Human_RBP_ID_24461804,Human_RBP_ID_24897068,Human_RBP_ID_26605369,Human_RBP_ID_27414325,Human_RBP_ID_27618954 Human_Splice_Rec_1258563 RMVar_hsa_circ_150673,RMVar_hsa_circ_377612,RMVar_hsa_circ_150677 56875 RMVar_ID_56875 Human_SNP_ID_470043938 m1A Human chr11 - 65503066 65503066 65503066 TGGCACACAGCACAGCCTCCTCAATCCACTTGATCCCAACTCATCTCTCATTTATTTCGGCTTCT TGGCACACAGCACAGCCTCCTCAATCCACTTGGTCCCAACTCATCTCTCATTTATTTCGGCTTCT T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,TALAM1-001:4,L13304-001,L13705-009,TALAM1-001:5,TALAM1-001:6 RNACentral:URS00008B3291,RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65502938..65503188 26863196 MeRIP-seq:(Medium) rs779378082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150672,RMVar_hsa_circ_150676 56876 RMVar_ID_56876 Human_SNP_ID_470043973 m1A Human chr11 - 65503124 65503123 65503125 TGAAATGAAGCAACTCTTCTGATAACGAAGAGATACCTGTCTGAGGCAAACGAAACATTGGCACA TGAAATGAAGCAACTCTTCTGATAACGAAGA__TACCTGTCTGAGGCAAACGAAACATTGGCACA ATC A TALAM1-001,TALAM1-001:2,TALAM1-001:3,TALAM1-001:4,L13304-001,L13705-009,TALAM1-001:5,TALAM1-001:6 RNACentral:URS00008B3291,RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65503051..65503275 32194978 MeRIP-seq:(Medium) rs1291987364 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_150672,RMVar_hsa_circ_150676 56877 RMVar_ID_56877 Human_SNP_ID_470043974 m1A Human chr11 - 65503124 65503124 65503124 TGAAATGAAGCAACTCTTCTGATAACGAAGAGATACCTGTCTGAGGCAAACGAAACATTGGCACA TGAAATGAAGCAACTCTTCTGATAACGAAGAGTTACCTGTCTGAGGCAAACGAAACATTGGCACA T A TALAM1-001,TALAM1-001:2,TALAM1-001:3,TALAM1-001:4,L13304-001,L13705-009,TALAM1-001:5,TALAM1-001:6 RNACentral:URS00008B3291,RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65503051..65503275 32194978 MeRIP-seq:(Medium) rs1031483096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150672,RMVar_hsa_circ_150676 56878 RMVar_ID_56878 Human_SNP_ID_470044366 m1A Human chr11 - 65503814 65503814 65503814 TATTATATGCTCATCACTTTATGAAGAATAAAATTTGTCTTTCCTGCCTTAAAGTTACATTCGTT TATTATATGCTCATCACTTTATGAAGAATAAACTTTGTCTTTCCTGCCTTAAAGTTACATTCGTT T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65503763..65503947 26863196 MeRIP-seq:(Medium) rs1387392182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150679,RMVar_hsa_circ_150676 56879 RMVar_ID_56879 Human_SNP_ID_470044616 m1A Human chr11 - 65504212 65504210 65504212 TATGCTGATAAACTCACTGCAAGGTCTCATACACTCACTAGAACAGAAGGAAGAGCCAAGCACTC TATGCTGATAAACTCACTGCAAGGTCTCATAC__TCACTAGAACAGAAGGAAGAGCCAAGCACTC AGT A TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65504161..65504337 26863196 MeRIP-seq:(Medium) rs757969692 Functional Loss DEL dbSNP153 33..34 33 - - - 56880 RMVar_ID_56880 Human_SNP_ID_470044617 m1A Human chr11 - 65504212 65504212 65504212 TATGCTGATAAACTCACTGCAAGGTCTCATACACTCACTAGAACAGAAGGAAGAGCCAAGCACTC TATGCTGATAAACTCACTGCAAGGTCTCATACGCTCACTAGAACAGAAGGAAGAGCCAAGCACTC T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65504161..65504337 26863196 MeRIP-seq:(Medium) rs376210739 Functional Loss SNV dbSNP153 33..33 33 - - - 56881 RMVar_ID_56881 Human_SNP_ID_470044618 m1A Human chr11 - 65504212 65504212 65504212 TATGCTGATAAACTCACTGCAAGGTCTCATACACTCACTAGAACAGAAGGAAGAGCCAAGCACTC TATGCTGATAAACTCACTGCAAGGTCTCATACCCTCACTAGAACAGAAGGAAGAGCCAAGCACTC T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65504161..65504337 26863196 MeRIP-seq:(Medium) rs376210739 Functional Loss SNV dbSNP153 33..33 33 - - - 56882 RMVar_ID_56882 Human_SNP_ID_470044969 m1A Human chr11 - 65504798 65504798 65504798 GCTGAGTGTTCCTGCATGTAAGAATTAAGACCAAGGGAGGGGAGAGAGAAACCCACACATAAACA GCTGAGTGTTCCTGCATGTAAGAATTAAGACCGAGGGAGGGGAGAGAGAAACCCACACATAAACA T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65504749..65504820 26863196 MeRIP-seq:(Medium) rs747819008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150688 56883 RMVar_ID_56883 Human_SNP_ID_470044970 m1A Human chr11 - 65504798 65504798 65504798 GCTGAGTGTTCCTGCATGTAAGAATTAAGACCAAGGGAGGGGAGAGAGAAACCCACACATAAACA GCTGAGTGTTCCTGCATGTAAGAATTAAGACCCAGGGAGGGGAGAGAGAAACCCACACATAAACA T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65504749..65504820 26863196 MeRIP-seq:(Medium) rs747819008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150688 56884 RMVar_ID_56884 Human_SNP_ID_470045140 m1A Human chr11 - 65505089 65505089 65505089 GCTCACATGCCAGTTACTCCAGCATAAAGCTGAAATCTATTCAATACTATTGTCCCATAACTGAT GCTCACATGCCAGTTACTCCAGCATAAAGCTGCAATCTATTCAATACTATTGTCCCATAACTGAT T G TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65505038..65505284 26863196 MeRIP-seq:(Medium) rs1334369851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150691 56885 RMVar_ID_56885 Human_SNP_ID_470045421 m1A Human chr11 - 65505553 65505553 65505553 CTAGATCAAAAGGCACGGGGTGGCGATGTGGCAGAGAAGTTGCTTGTGGGGAGACCTTGCTTTTA CTAGATCAAAAGGCACGGGGTGGCGATGTGGCGGAGAAGTTGCTTGTGGGGAGACCTTGCTTTTA T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65505438..65505957 26863196 MeRIP-seq:(Medium) rs1016390841 Functional Loss SNV dbSNP153 33..33 33 - - - 56886 RMVar_ID_56886 Human_SNP_ID_470045445 m1A Human chr11 + 65505587 65505587 65505587 CCACATCGCCACCCCGTGCCTTTTGATCTAGCACAGACCCTTCACCCCTCACCTCGATGCAGCCA CCACATCGCCACCCCGTGCCTTTTGATCTAGCGCAGACCCTTCACCCCTCACCTCGATGCAGCCA A G MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65505453..65505650 26863196 MeRIP-seq:(Medium) rs375211855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228236,Human_RBP_ID_751116,Human_RBP_ID_807132,Human_RBP_ID_1080624,Human_RBP_ID_1459276,Human_RBP_ID_2276176,Human_RBP_ID_3388422,Human_RBP_ID_4171906,Human_RBP_ID_5087015,Human_RBP_ID_5169396,Human_RBP_ID_5549997,Human_RBP_ID_6086264,Human_RBP_ID_8177201,Human_RBP_ID_8355919,Human_RBP_ID_9005482,Human_RBP_ID_9644987,Human_RBP_ID_11674058,Human_RBP_ID_17108748,Human_RBP_ID_17184765,Human_RBP_ID_18610985,Human_RBP_ID_19583097,Human_RBP_ID_22164923,Human_RBP_ID_22381304,Human_RBP_ID_22791793,Human_RBP_ID_22893145,Human_RBP_ID_23515170,Human_RBP_ID_24404313,Human_RBP_ID_24461873,Human_RBP_ID_24897203,Human_RBP_ID_26405947,Human_RBP_ID_26894601,Human_RBP_ID_27205006,Human_RBP_ID_27414382 Human_Splice_Rec_1258579,Human_Splice_Rec_1258582,Human_Splice_Rec_1258583,Human_Splice_Rec_1258585 Human_miRNA_ID_3158866,Human_miRNA_ID_3196947,Human_miRNA_ID_3209500 RMVar_hsa_circ_150687,RMVar_hsa_circ_150695,RMVar_hsa_circ_150698,RMVar_hsa_circ_150699 56887 RMVar_ID_56887 Human_SNP_ID_470045603 m1A Human chr11 + 65505836 65505836 65505836 TTAAACCAGTAAGTGGAGAAATAACATGTTCAAGAACTGTAATGCTGGGTGGGAACATGTAACTT TTAAACCAGTAAGTGGAGAAATAACATGTTCATGAACTGTAATGCTGGGTGGGAACATGTAACTT A T MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65505786..65505956 26863196 MeRIP-seq:(Medium) rs370754223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1079333,Human_RBP_ID_1459286,Human_RBP_ID_1781506,Human_RBP_ID_2276176,Human_RBP_ID_3378123,Human_RBP_ID_5550000,Human_RBP_ID_6086272,Human_RBP_ID_8355924,Human_RBP_ID_9005482,Human_RBP_ID_9644989,Human_RBP_ID_10482325,Human_RBP_ID_11674076,Human_RBP_ID_17062325,Human_RBP_ID_17108752,Human_RBP_ID_17184765,Human_RBP_ID_17465779,Human_RBP_ID_17581387,Human_RBP_ID_17682414,Human_RBP_ID_18610991,Human_RBP_ID_19583102,Human_RBP_ID_21916498,Human_RBP_ID_22032870,Human_RBP_ID_22164926,Human_RBP_ID_22381306,Human_RBP_ID_22791801,Human_RBP_ID_22893154,Human_RBP_ID_23515190,Human_RBP_ID_24404325,Human_RBP_ID_24461909,Human_RBP_ID_24897203,Human_RBP_ID_26405953,Human_RBP_ID_26894605,Human_RBP_ID_27414390,Human_RBP_ID_27618994 Human_miRNA_ID_3175930,Human_miRNA_ID_3204430 RMVar_hsa_circ_150698,RMVar_hsa_circ_150699,RMVar_hsa_circ_150702 56888 RMVar_ID_56888 Human_SNP_ID_470045785 m1A Human chr11 + 65506159 65506159 65506159 GTTGGCACTCCTGGTTTCCAGGACGGGGTTCAAATCCCTGCGGCGTCTTTGCTTTGACTACTAAT GTTGGCACTCCTGGTTTCCAGGACGGGGTTCACATCCCTGCGGCGTCTTTGCTTTGACTACTAAT A C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs768156015 Functional Loss SNV dbSNP153 33..33 33 - - - 56889 RMVar_ID_56889 Human_SNP_ID_470045786 m1A Human chr11 + 65506159 65506159 65506159 GTTGGCACTCCTGGTTTCCAGGACGGGGTTCAAATCCCTGCGGCGTCTTTGCTTTGACTACTAAT GTTGGCACTCCTGGTTTCCAGGACGGGGTTCATATCCCTGCGGCGTCTTTGCTTTGACTACTAAT A T TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs768156015 Functional Loss SNV dbSNP153 33..33 33 - - - 56890 RMVar_ID_56890 Human_SNP_ID_470045794 m1A Human chr11 - 65506176 65506172 65506177 AAGAGTCCTGAAGACAGATTAGTAGTCAAAGCAAAGACGCCGCAGGGATTTGAACCCCGTCCTGG AAGAGTCCTGAAGACAGATTAGTAGTCAAAG_____ACGCCGCAGGGATTTGAACCCCGTCCTGG TCTTTG T TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65506126..65506225 26863196 MeRIP-seq:(Medium) rs1250718881 Functional Loss DEL dbSNP153 32..36 33 - - - 56891 RMVar_ID_56891 Human_SNP_ID_470045813 m1A Human chr11 + 65506200 65506200 65506200 GGCGTCTTTGCTTTGACTACTAATCTGTCTTCAGGACTCTTTCTGTATTTCTCCTTTTCTCTGCA GGCGTCTTTGCTTTGACTACTAATCTGTCTTCGGGACTCTTTCTGTATTTCTCCTTTTCTCTGCA A G MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65506101..65506350 26863196 MeRIP-seq:(Medium) rs763414958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2276193,Human_RBP_ID_8355940,Human_RBP_ID_19583110,Human_RBP_ID_24461923,Human_RBP_ID_24897238 56892 RMVar_ID_56892 Human_SNP_ID_470045834 m1A Human chr11 + 65506239 65506239 65506239 TTTCTGTATTTCTCCTTTTCTCTGCAGGTGCTAGTTCTTGGAGTTTTGGGGAGGTGGGAGGTAAC TTTCTGTATTTCTCCTTTTCTCTGCAGGTGCTGGTTCTTGGAGTTTTGGGGAGGTGGGAGGTAAC A G MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65506201..65506300 26863196 MeRIP-seq:(Medium) rs1251410814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24897238 Human_miRNA_ID_3151808,Human_miRNA_ID_3202359 56893 RMVar_ID_56893 Human_SNP_ID_470045848 m1A Human chr11 + 65506269 65506268 65506269 CTAGTTCTTGGAGTTTTGGGGAGGTGGGAGGTAACAGCACAATATCTTTGAACTATATACATCCT CTAGTTCTTGGAGTTTTGGGGAGGTGGGAGGT_ACAGCACAATATCTTTGAACTATATACATCCT TA T MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:65506167..65506400 26863410 MeRIP-seq:(Medium) rs756344756 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1163041,Human_RBP_ID_5093193,Human_RBP_ID_6086299,Human_RBP_ID_11674112,Human_RBP_ID_16987174,Human_RBP_ID_24461924,Human_RBP_ID_24918124 Human_Splice_Rec_1258550 56894 RMVar_ID_56894 Human_SNP_ID_470045887 m1A Human chr11 + 65506345 65506345 65506345 TTGTCAGGAGCTTGACTTGATTGTATATTCATATTTACACGAGAACCTAATATAACTGCCTTGTC TTGTCAGGAGCTTGACTTGATTGTATATTCATGTTTACACGAGAACCTAATATAACTGCCTTGTC A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65506248..65506375 26863410 MeRIP-seq:(Medium) rs1468762536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2295878,Human_RBP_ID_23515242 Human_Splice_Rec_1258550 56895 RMVar_ID_56895 Human_SNP_ID_470051324 m1A Human chr11 + 65525151 65525151 65525151 CTAAGGCGCCCGAACCCGCGGCGGCGGTGGGGACGATGTGGTTCTTTGCCCGGGACCCGGTCCGG CTAAGGCGCCCGAACCCGCGGCGGCGGTGGGGTCGATGTGGTTCTTTGCCCGGGACCCGGTCCGG A T SCYL1 Ensembl:ENSG00000142186 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65525101..65525298 26863196 MeRIP-seq:(Medium) rs753254030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184198,Human_RBP_ID_5314289 56896 RMVar_ID_56896 Human_SNP_ID_470051329 m1A Human chr11 - 65525165 65525165 65525165 TCGAACGGAAAGTCCCGGACCGGGTCCCGGGCAAAGAACCACATCGTCCCCACCGCCGCCGCGGG TCGAACGGAAAGTCCCGGACCGGGTCCCGGGCGAAGAACCACATCGTCCCCACCGCCGCCGCGGG T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65525133..65525291 26863196 MeRIP-seq:(Medium) rs1234482408 Functional Loss SNV dbSNP153 33..33 33 - - - 56897 RMVar_ID_56897 Human_SNP_ID_470054937 m1A Human chr11 + 65537848 65537848 65537848 CCGAGTCTGTGCTGGCCCAGCAGGACGACTGGAGCACCGGGGGCCAAGTGAGCCGTGCTAGTCAG CCGAGTCTGTGCTGGCCCAGCAGGACGACTGGGGCACCGGGGGCCAAGTGAGCCGTGCTAGTCAG A G SCYL1 Ensembl:ENSG00000142186 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65537826..65537900 26863196 MeRIP-seq:(Medium) rs1300073968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940772,Human_RBP_ID_18972227,Human_RBP_ID_26318733 Human_Splice_Rec_1258614,Human_Splice_Rec_1258615,Human_Splice_Rec_1258646,Human_Splice_Rec_1258647,Human_Splice_Rec_1258680,Human_Splice_Rec_1258681,Human_Splice_Rec_1258714,Human_Splice_Rec_1258715,Human_Splice_Rec_1258748,Human_Splice_Rec_1258749,Human_Splice_Rec_1258778,Human_Splice_Rec_1258779,Human_Splice_Rec_1258798,Human_Splice_Rec_1258799,Human_Splice_Rec_1258820,Human_Splice_Rec_1258821,Human_Splice_Rec_1258844,Human_Splice_Rec_1258845,Human_Splice_Rec_1258851 Human_miRNA_ID_2479106 RMVar_hsa_circ_101730,RMVar_hsa_circ_150704,RMVar_hsa_circ_97162,RMVar_hsa_circ_150706 56898 RMVar_ID_56898 Human_SNP_ID_470055277 m1A Human chr11 + 65538493 65538493 65538493 GGCCCGGAAGAAGCGCGAGGAGCGGCGGCGGGAGATGGAGGCCAAACGCGCCGAGAGGAAGGTGG GGCCCGGAAGAAGCGCGAGGAGCGGCGGCGGGGGATGGAGGCCAAACGCGCCGAGAGGAAGGTGG A G SCYL1 Ensembl:ENSG00000142186 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65538426..65538595 26863196 MeRIP-seq:(Medium) rs200041750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809017,Human_RBP_ID_8774356,Human_RBP_ID_9362502,Human_RBP_ID_18159267,Human_RBP_ID_18188291,Human_RBP_ID_18974071,Human_RBP_ID_26320185,Human_RBP_ID_27205025 Human_Splice_Rec_1258618,Human_Splice_Rec_1258652,Human_Splice_Rec_1258686,Human_Splice_Rec_1258720,Human_Splice_Rec_1258784,Human_Splice_Rec_1258804,Human_Splice_Rec_1258850,Human_Splice_Rec_1258856 RMVar_hsa_circ_101730,RMVar_hsa_circ_150704 56899 RMVar_ID_56899 Human_SNP_ID_470055340 m1A Human chr11 + 65538598 65538598 65538598 AACCGTGGCGGTGGCCCTTCCCGGCTGCGGAGAGCCCGCCCCACAGATGTATTTATTGTACAAAC AACCGTGGCGGTGGCCCTTCCCGGCTGCGGAGGGCCCGCCCCACAGATGTATTTATTGTACAAAC A G SCYL1 Ensembl:ENSG00000142186 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65538551..65538650 32194978 MeRIP-seq:(Medium) rs1268900363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400864,Human_RBP_ID_809018,Human_RBP_ID_865958,Human_RBP_ID_5110504,Human_RBP_ID_18159854,Human_RBP_ID_18611005,Human_RBP_ID_21883059 Human_miRNA_ID_2386871,Human_miRNA_ID_2388347,Human_miRNA_ID_2399497,Human_miRNA_ID_3030551 RMVar_hsa_circ_101730,RMVar_hsa_circ_150704 56900 RMVar_ID_56900 Human_SNP_ID_470055545 m1A Human chr11 - 65539041 65539041 65539041 CGACGCCGCCCTCGGCCCAGACCTCGGTGATCACTGAGGGATTTCCGCGAGCTCGGCCTCACTTC CGACGCCGCCCTCGGCCCAGACCTCGGTGATCGCTGAGGGATTTCCGCGAGCTCGGCCTCACTTC T C LTBP3 Ensembl:ENSG00000168056 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65539008..65539119 26863196 MeRIP-seq:(Medium) rs1344461987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400870 56901 RMVar_ID_56901 Human_SNP_ID_470055979 m1A Human chr11 + 65539802 65539802 65539802 TGGCGGCAGCAGCAGTCGTCGAAGGTGAGGGCAGGCCCGGCCAGGGGGCCAGCGCACATGCCGTC TGGCGGCAGCAGCAGTCGTCGAAGGTGAGGGCGGGCCCGGCCAGGGGGCCAGCGCACATGCCGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65539751..65539881 26863196 MeRIP-seq:(Medium) rs1208346750 Functional Loss SNV dbSNP153 33..33 33 - - - 56902 RMVar_ID_56902 Human_SNP_ID_470056435 m1A Human chr11 + 65540580 65540580 65540580 GGCTGCGTGTTCACGCACTTGCCCTCCTTGCAAATCTCCGACCCGAACAACATGCACTCGTCGAT GGCTGCGTGTTCACGCACTTGCCCTCCTTGCAGATCTCCGACCCGAACAACATGCACTCGTCGAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65540549..65540634 26863196 MeRIP-seq:(Medium) rs151139557 Functional Loss SNV dbSNP153 33..33 33 - - - 56903 RMVar_ID_56903 Human_SNP_ID_470056895 m1A Human chr11 + 65541604 65541604 65541604 CCGAGGGAGGAGCTGGGAGGACACTCACCCTCACAACCGTGCTGGTCCTGGGTGGGAGTGAAGCC CCGAGGGAGGAGCTGGGAGGACACTCACCCTCGCAACCGTGCTGGTCCTGGGTGGGAGTGAAGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65541601..65541725 32194978 MeRIP-seq:(Medium) rs570025632 Functional Loss SNV dbSNP153 33..33 33 - - - 56904 RMVar_ID_56904 Human_SNP_ID_470057764 m1A Human chr11 + 65544612 65544611 65544612 GCACCTCCCTCTCTGACTCCTCTAAAGCTTTGACTTCCATAAAGCCCCTAGGCAGCCCCATGCCC GCACCTCCCTCTCTGACTCCTCTAAAGCTTTG_CTTCCATAAAGCCCCTAGGCAGCCCCATGCCC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65544610..65544999 26863196 MeRIP-seq:(Medium) rs1435509486 Functional Loss DEL dbSNP153 33..33 33 - - - 56905 RMVar_ID_56905 Human_SNP_ID_470058060 m1A Human chr11 + 65545948 65545948 65545948 CTGATCTGCCAGTGCCAACCCCTGTGCCTGCCATGCTGTTCCTCTCCTCCTTTCTTGCCCAATTC CTGATCTGCCAGTGCCAACCCCTGTGCCTGCCGTGCTGTTCCTCTCCTCCTTTCTTGCCCAATTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65545942..65546065 26863196 MeRIP-seq:(Medium) rs547557437 Functional Loss SNV dbSNP153 33..33 33 - - - 56906 RMVar_ID_56906 Human_SNP_ID_470058192 m1A Human chr11 - 65546451 65546451 65546451 CCCAGGGCTACGCGCCCGCGCCCGACGGCCGCAGTTGCTTGGGTGAGCGCCAGCACCCCCGCCCC CCCAGGGCTACGCGCCCGCGCCCGACGGCCGCGGTTGCTTGGGTGAGCGCCAGCACCCCCGCCCC T C LTBP3 Ensembl:ENSG00000168056 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65546436..65546587 32194978 MeRIP-seq:(Medium) rs763878267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5343928,Human_RBP_ID_19052171,Human_RBP_ID_26318734 Human_Splice_Rec_1258887,Human_Splice_Rec_1258957,Human_Splice_Rec_1259005,Human_Splice_Rec_1259035,Human_Splice_Rec_1259089,Human_Splice_Rec_1259131,Human_Splice_Rec_1259201 RMVar_hsa_circ_47030,RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 56907 RMVar_ID_56907 Human_SNP_ID_470058849 m1A Human chr11 - 65548002 65548002 65548002 TGCCGACTGAACCAGAACATCTGTGGCCACGGAGAGTGCGTGCCGGGCCCCCCTGACTACTCCTG TGCCGACTGAACCAGAACATCTGTGGCCACGGGGAGTGCGTGCCGGGCCCCCCTGACTACTCCTG T C LTBP3 Ensembl:ENSG00000168056 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr11:65547856..65548093;chr11:65547951..65548759 26863196 MeRIP-seq:(Medium) rs947287396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1258878,Human_Splice_Rec_1258879,Human_Splice_Rec_1258948,Human_Splice_Rec_1258949,Human_Splice_Rec_1259027,Human_Splice_Rec_1259080,Human_Splice_Rec_1259081,Human_Splice_Rec_1259122,Human_Splice_Rec_1259123,Human_Splice_Rec_1259192,Human_Splice_Rec_1259193,Human_Splice_Rec_1259238,Human_Splice_Rec_1259244 Human_miRNA_ID_2027315,Human_miRNA_ID_2464944 RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 56908 RMVar_ID_56908 Human_SNP_ID_470058857 m1A Human chr11 + 65548027 65548027 65548027 CGCACTCTCCGTGGCCACAGATGTTCTGGTTCAGTCGGCACTCATCAGTCTCTGCGGGCATGGCC CGCACTCTCCGTGGCCACAGATGTTCTGGTTCTGTCGGCACTCATCAGTCTCTGCGGGCATGGCC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:65547837..65548100 26863196 MeRIP-seq:(Medium) rs1196174248 Functional Loss SNV dbSNP153 33..33 33 - - - 56909 RMVar_ID_56909 Human_SNP_ID_470058867 m1A Human chr11 - 65548045 65548045 65548045 TGCTCTGCCGCTTGACCTGGCCATGCCCGCAGAGACTGATGAGTGCCGACTGAACCAGAACATCT TGCTCTGCCGCTTGACCTGGCCATGCCCGCAGTGACTGATGAGTGCCGACTGAACCAGAACATCT T A LTBP3 Ensembl:ENSG00000168056 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65548012..65548763 26863196 MeRIP-seq:(Medium) rs1378569789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11674203,Human_RBP_ID_22641576 Human_Splice_Rec_1258878,Human_Splice_Rec_1258948,Human_Splice_Rec_1259080,Human_Splice_Rec_1259122,Human_Splice_Rec_1259192,Human_Splice_Rec_1259238,Human_Splice_Rec_1259244 RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 56910 RMVar_ID_56910 Human_SNP_ID_470061591 m1A Human chr11 + 65557733 65557733 65557733 CCTGCTGACAACTGTCCCGACACTGGCCCTTGAGACAGGTCCGCTTGCAGATCACCGGCGCAAAG CCTGCTGACAACTGTCCCGACACTGGCCCTTGCGACAGGTCCGCTTGCAGATCACCGGCGCAAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65557702..65557796 26863196 MeRIP-seq:(Medium) rs781256863 Functional Loss SNV dbSNP153 33..33 33 - - - 56911 RMVar_ID_56911 Human_SNP_ID_470061592 m1A Human chr11 + 65557733 65557733 65557733 CCTGCTGACAACTGTCCCGACACTGGCCCTTGAGACAGGTCCGCTTGCAGATCACCGGCGCAAAG CCTGCTGACAACTGTCCCGACACTGGCCCTTGTGACAGGTCCGCTTGCAGATCACCGGCGCAAAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65557702..65557796 26863196 MeRIP-seq:(Medium) rs781256863 Functional Loss SNV dbSNP153 33..33 33 - - - 56912 RMVar_ID_56912 Human_SNP_ID_470061788 m1A Human chr11 - 65558288 65558287 65558288 CGCGGCCGCGGGAGAGGAGCCCGGCCAGGGGGAGGCGCGGAGCGGGCCGGCCGCCCGGCCTTCCT CGCGGCCGCGGGAGAGGAGCCCGGCCAGGGGG_GGCGCGGAGCGGGCCGGCCGCCCGGCCTTCCT CT C LTBP3 Ensembl:ENSG00000168056 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:65558118..65558350 26863410 MeRIP-seq:(Medium) rs1474358070 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_226975,Human_RBP_ID_807737,Human_RBP_ID_4184202,Human_RBP_ID_18416925,Human_RBP_ID_18933693,Human_RBP_ID_21965404,Human_RBP_ID_22433755 RMVar_hsa_circ_94130,RMVar_hsa_circ_76641,RMVar_hsa_circ_150708,RMVar_hsa_circ_150712 56913 RMVar_ID_56913 Human_SNP_ID_470064445 m1A Human chr11 + 65568912 65568912 65568912 GACTCATGTAAGGCTCTTTGTAGGTGCGAGGCAGAATAGACAGTTGAGTGGATATTGGCCATGAT GACTCATGTAAGGCTCTTTGTAGGTGCGAGGCGGAATAGACAGTTGAGTGGATATTGGCCATGAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65568879..65569029 26863196 MeRIP-seq:(Medium) rs1271882147 Functional Loss SNV dbSNP153 33..33 33 - - - 56914 RMVar_ID_56914 Human_SNP_ID_470064674 m1A Human chr11 - 65569809 65569809 65569809 GTTGAAATCCTCAAAAAGCCTGCAGACTGAATAGCGCTGTACTGGGCACGCGCATTGCGCTTCCA GTTGAAATCCTCAAAAAGCCTGCAGACTGAATGGCGCTGTACTGGGCACGCGCATTGCGCTTCCA T C ZNRD2-AS1 Ensembl:ENSG00000260233 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65569775..65569990 26863196 MeRIP-seq:(Medium) rs1432038798 Functional Loss SNV dbSNP153 33..33 33 - - - 56915 RMVar_ID_56915 Human_SNP_ID_470064987 m1A Human chr11 - 65570509 65570509 65570509 AGCCACAAACCCCTGCCGCCCAGGTCCTCACCAGCTCCGTTCAGGGCCATGTTGCCGTTGTCACC AGCCACAAACCCCTGCCGCCCAGGTCCTCACCCGCTCCGTTCAGGGCCATGTTGCCGTTGTCACC T G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr11:65570505..65570726;chr11:65570476..65570750 26863196 MeRIP-seq:(Medium) rs1287849261 Functional Loss SNV dbSNP153 33..33 33 - - - 56916 RMVar_ID_56916 Human_SNP_ID_470065089 m1A Human chr11 + 65570706 65570706 65570706 GCAAGATCGCATCTCCCGGCTCATGGGCGACTATCTGCTGCGCGGTTACCGCATGCTGGGCGAGA GCAAGATCGCATCTCCCGGCTCATGGGCGACTGTCTGCTGCGCGGTTACCGCATGCTGGGCGAGA A G ZNRD2 Ensembl:ENSG00000173465 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65570527..65571725 32194978 MeRIP-seq:(Medium) rs961571891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4172123,Human_RBP_ID_9363772 Human_Splice_Rec_1259277,Human_Splice_Rec_1259283,Human_Splice_Rec_1259287,Human_Splice_Rec_1259293,Human_Splice_Rec_1259297,Human_Splice_Rec_1259303 RMVar_hsa_circ_126365,RMVar_hsa_circ_150713 56917 RMVar_ID_56917 Human_SNP_ID_470065166 m1A Human chr11 - 65570879 65570879 65570879 CGCTGTTTGTCTTGGAGGAGGATCGTCTACGGACCAAAAAGCACACGGGGCCGGAATGAGACGCC CGCTGTTTGTCTTGGAGGAGGATCGTCTACGGCCCAAAAAGCACACGGGGCCGGAATGAGACGCC T G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65570876..65570950 26863196 MeRIP-seq:(Medium) rs1207977039 Functional Loss SNV dbSNP153 33..33 33 - - - 56918 RMVar_ID_56918 Human_SNP_ID_470065664 m1A Human chr11 - 65572574 65572574 65572574 CCCGCAGGCCCCGCACCCCGCGGCCCCGCCGGAGCCCAGCCGCCGCCCGCAGGCCTCGCTTTGTT CCCGCAGGCCCCGCACCCCGCGGCCCCGCCGGCGCCCAGCCGCCGCCCGCAGGCCTCGCTTTGTT T G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65572539..65572932;chr11:65572488..65572955 26863196 MeRIP-seq:(Medium) rs576638846 Functional Loss SNV dbSNP153 33..33 33 - - - 56919 RMVar_ID_56919 Human_SNP_ID_470065668 m1A Human chr11 - 65572592 65572577 65572592 GCTCCGCCCGGGCCGCCGCCCGCAGGCCCCGCACCCCGCGGCCCCGCCGGAGCCCAGCCGCCGCC GCTCCGCCCGGGCCGCCGCCCGCAGGCCCCGC_______________CGGAGCCCAGCCGCCGCC GGCGGGGCCGCGGGGT G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65572463..65572950 26863196 MeRIP-seq:(Medium) rs1174943198 Functional Loss DEL dbSNP153 33..47 33 - - - 56920 RMVar_ID_56920 Human_SNP_ID_470065675 m1A Human chr11 - 65572592 65572592 65572592 GCTCCGCCCGGGCCGCCGCCCGCAGGCCCCGCACCCCGCGGCCCCGCCGGAGCCCAGCCGCCGCC GCTCCGCCCGGGCCGCCGCCCGCAGGCCCCGCCCCCCGCGGCCCCGCCGGAGCCCAGCCGCCGCC T G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65572463..65572950 26863196 MeRIP-seq:(Medium) rs893803820 Functional Loss SNV dbSNP153 33..33 33 - - - 56921 RMVar_ID_56921 Human_SNP_ID_470065694 m1A Human chr11 - 65572646 65572646 65572646 CCCGTTCATGGCCGGGGCCGGCGCGGACGGCGATGCCACCTCCTTCCCTCCAACGCTCCGCCCGG CCCGTTCATGGCCGGGGCCGGCGCGGACGGCGCTGCCACCTCCTTCCCTCCAACGCTCCGCCCGG T G L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:65572560..65572662 26863410 MeRIP-seq:(Medium) rs1373108655 Functional Loss SNV dbSNP153 33..33 33 - - - 56922 RMVar_ID_56922 Human_SNP_ID_470065957 m1A Human chr11 - 65573420 65573420 65573420 GTCTTGGCACAGGTGTTTGTAGTCCTGGATTGACTCGTACAGGCCCCACAGCTGGCACAACAAGG GTCTTGGCACAGGTGTTTGTAGTCCTGGATTGGCTCGTACAGGCCCCACAGCTGGCACAACAAGG T C L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65572737..65574101 32194978 MeRIP-seq:(Medium) rs775060624 Functional Loss SNV dbSNP153 33..33 33 - - - 56923 RMVar_ID_56923 Human_SNP_ID_470065967 m1A Human chr11 + 65573448 65573448 65573448 CGAGTCAATCCAGGACTACAAACACCTGTGCCAAGACCTGAGCTTCTGCCAGGACCTGTCATCCT CGAGTCAATCCAGGACTACAAACACCTGTGCCCAGACCTGAGCTTCTGCCAGGACCTGTCATCCT A C ZNRD2,FAM89B Ensembl:ENSG00000173465,Ensembl:ENSG00000176973 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65573417..65573542 26863196 MeRIP-seq:(Medium) rs1212790742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4172194,Human_RBP_ID_8355983,Human_RBP_ID_26803781 Human_Splice_Rec_1259306,Human_Splice_Rec_1259310,Human_Splice_Rec_1259312,Human_Splice_Rec_1259314 56924 RMVar_ID_56924 Human_SNP_ID_470066149 m1A Human chr11 + 65573970 65573970 65573970 CTTCCCTTCCGCTTGGCGTCTCTGGGATTGGGATGAGTGCCTGGCTCCCATCTCCTCCTCACCTT CTTCCCTTCCGCTTGGCGTCTCTGGGATTGGGGTGAGTGCCTGGCTCCCATCTCCTCCTCACCTT A G FAM89B Ensembl:ENSG00000176973 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65573934..65574089 26863196 MeRIP-seq:(Medium) rs930114907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400891,Human_RBP_ID_5138972,Human_RBP_ID_17682418,Human_RBP_ID_17799248,Human_RBP_ID_23515299 Human_miRNA_ID_845675,Human_miRNA_ID_1384310 56925 RMVar_ID_56925 Human_SNP_ID_470068197 m1A Human chr11 + 65580442 65580442 65580442 GCTGAGAGTGATGAAGATGAGGCTCATGGCCCAGGAGCCCCGGAGGCCCGGGCTCGAGTCCCCCA GCTGAGAGTGATGAAGATGAGGCTCATGGCCCGGGAGCCCCGGAGGCCCGGGCTCGAGTCCCCCA A G EHBP1L1 Ensembl:ENSG00000173442 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65580326..65581364 26863196 MeRIP-seq:(Medium) rs1565120915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400897,Human_RBP_ID_869657,Human_RBP_ID_3940792,Human_RBP_ID_8773703,Human_RBP_ID_9276515,Human_RBP_ID_18974103 Human_Splice_Rec_1259325,Human_Splice_Rec_1259345,Human_Splice_Rec_1259381 Human_miRNA_ID_2040165,Human_miRNA_ID_3019147 RMVar_hsa_circ_12906,RMVar_hsa_circ_362176,RMVar_hsa_circ_150716,RMVar_hsa_circ_95072 56926 RMVar_ID_56926 Human_SNP_ID_470068451 m1A Human chr11 - 65581140 65581140 65581140 TGACCTGGGGTCCAGTCTCCACCCCCAACCCCAGCCTGGGTCTCACCTGCCTGCTGGGGTCGTCC TGACCTGGGGTCCAGTCTCCACCCCCAACCCCGGCCTGGGTCTCACCTGCCTGCTGGGGTCGTCC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65581136..65581241 26863196 MeRIP-seq:(Medium) rs772366488 Functional Loss SNV dbSNP153 33..33 33 - - - 56927 RMVar_ID_56927 Human_SNP_ID_470068653 m1A Human chr11 + 65581620 65581620 65581620 CTCCGGAAAGGCTCTGATGCCCTCCGGCCCCCAGTCCCCCAGGGGGAAGATGAGGTCCCCAAAGC CTCCGGAAAGGCTCTGATGCCCTCCGGCCCCCCGTCCCCCAGGGGGAAGATGAGGTCCCCAAAGC A C EHBP1L1 Ensembl:ENSG00000173442 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65581551..65581975 32194978 MeRIP-seq:(Medium) rs1295271938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18611024 Human_Splice_Rec_1259330,Human_Splice_Rec_1259350 Human_miRNA_ID_1321251 RMVar_hsa_circ_12906,RMVar_hsa_circ_362176 56928 RMVar_ID_56928 Human_SNP_ID_470068745 m1A Human chr11 + 65581881 65581881 65581881 GACACTGAGCCAAGGTCAGGAGGCAGAGAGGCAAACACTAAGAGGTCAGGAGTCAGAGCTGGGGA GACACTGAGCCAAGGTCAGGAGGCAGAGAGGCGAACACTAAGAGGTCAGGAGTCAGAGCTGGGGA A G EHBP1L1 Ensembl:ENSG00000173442 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65581701..65583485 26863196 MeRIP-seq:(Medium) rs370827866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2598,Human_RBP_ID_11674384 Human_Splice_Rec_1259397 RMVar_hsa_circ_12906,RMVar_hsa_circ_362176 56929 RMVar_ID_56929 Human_SNP_ID_470068977 m1A Human chr11 + 65582476 65582476 65582476 GGTCAGGGTTCCCAGAGACTAGGACACTAGAAATTGAGATATTGGGGGCCTTGGAGAAAGAAGCA GGTCAGGGTTCCCAGAGACTAGGACACTAGAAGTTGAGATATTGGGGGCCTTGGAGAAAGAAGCA A G EHBP1L1 Ensembl:ENSG00000173442 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65582150..65582633 26863196 MeRIP-seq:(Medium) rs750780923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1265395,Human_RBP_ID_11674396,Human_RBP_ID_17799252,Human_RBP_ID_18932603,Human_RBP_ID_26409709 RMVar_hsa_circ_12906,RMVar_hsa_circ_362176 56930 RMVar_ID_56930 Human_SNP_ID_470069939 m1A Human chr11 - 65584971 65584971 65584971 CTCCAGCAGCCGCGACACGCCCAGAGCCGCGAAGCCATCGAAGGCCTAGGGGAAGGGTGCACTCG CTCCAGCAGCCGCGACACGCCCAGAGCCGCGAGGCCATCGAAGGCCTAGGGGAAGGGTGCACTCG T C L13304-001,L13705-009,lnc-KCNK7-1 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS0000D57E66 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65584969..65585067 26863196 MeRIP-seq:(Medium) rs1229060450 Functional Loss SNV dbSNP153 33..33 33 - - - 56931 RMVar_ID_56931 Human_SNP_ID_470070012 m1A Human chr11 + 65585133 65585133 65585133 TGGTACAACTGGAGGGCGGCGGCGGCGCCGGCACGTACCGCGTGGGCAGCGCCCAGCCCAGCCCG TGGTACAACTGGAGGGCGGCGGCGGCGCCGGCTCGTACCGCGTGGGCAGCGCCCAGCCCAGCCCG A T EHBP1L1 Ensembl:ENSG00000173442 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65585082..65585158 26863196 MeRIP-seq:(Medium) rs1485660316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867756,Human_RBP_ID_9362506,Human_RBP_ID_24542913 Human_miRNA_ID_2391788 RMVar_hsa_circ_362176,RMVar_hsa_circ_87671,RMVar_hsa_circ_116880,RMVar_hsa_circ_150717,RMVar_hsa_circ_150718 56932 RMVar_ID_56932 Human_SNP_ID_470074360 m1A Human chr11 + 65598468 65598468 65598468 CGGCGGGGTGCAGGCTGTGGTGATGGCAGGGGAGAAGGCCGTGGCCCAGCTGACACAAAGCTCCA CGGCGGGGTGCAGGCTGTGGTGATGGCAGGGGGGAAGGCCGTGGCCCAGCTGACACAAAGCTCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65598433..65599716 26863196 MeRIP-seq:(Medium) rs200098330 Functional Loss SNV dbSNP153 33..33 33 - - - 56933 RMVar_ID_56933 Human_SNP_ID_470074405 m1A Human chr11 - 65598576 65598574 65598576 CCGGGGACATCACGCTCTGCTCCTGGCACCCCAGGCACCCCACGTTCACCACCCCTGGGCCTCAT CCGGGGACATCACGCTCTGCTCCTGGCACCCC__GCACCCCACGTTCACCACCCCTGGGCCTCAT CCT C MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65598476..65599666 26863410 MeRIP-seq:(Medium) rs1377033420 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_400905,Human_RBP_ID_27414449 Human_Splice_Rec_1259454,Human_Splice_Rec_1259472,Human_Splice_Rec_1259490 RMVar_hsa_circ_88825,RMVar_hsa_circ_96634,RMVar_hsa_circ_127176,RMVar_hsa_circ_93686,RMVar_hsa_circ_150719,RMVar_hsa_circ_150721,RMVar_hsa_circ_150722,RMVar_hsa_circ_150720 56934 RMVar_ID_56934 Human_SNP_ID_470074666 m1A Human chr11 - 65599423 65599423 65599423 CCTGGGTATCCCTGTGGGCCAGCGGTCAGCCAAGAGCCCCCGACGTGAGGAGGAGCCCCGCGGTG CCTGGGTATCCCTGTGGGCCAGCGGTCAGCCAGGAGCCCCCGACGTGAGGAGGAGCCCCGCGGTG T C MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65598404..65599616 26863196 MeRIP-seq:(Medium) rs753282799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750414,Human_RBP_ID_17350633,Human_RBP_ID_18933695 Human_Splice_Rec_1259453,Human_Splice_Rec_1259471,Human_Splice_Rec_1259489,Human_Splice_Rec_1259505 RMVar_hsa_circ_88825,RMVar_hsa_circ_96634,RMVar_hsa_circ_127176,RMVar_hsa_circ_93686,RMVar_hsa_circ_150719,RMVar_hsa_circ_150721,RMVar_hsa_circ_150722,RMVar_hsa_circ_150720,RMVar_hsa_circ_33691 56935 RMVar_ID_56935 Human_SNP_ID_470074711 m1A Human chr11 + 65599508 65599508 65599508 AGTGGGCGGGGAGTCGGGCGTCTTGAGCGAGAAGCAGATGAGCGGGGAAGGGGGCGGCTCGGTCG AGTGGGCGGGGAGTCGGGCGTCTTGAGCGAGAGGCAGATGAGCGGGGAAGGGGGCGGCTCGGTCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65598388..65599616 26863196 MeRIP-seq:(Medium) rs374223116 Functional Loss SNV dbSNP153 33..33 33 - - - 56936 RMVar_ID_56936 Human_SNP_ID_470076550 m1A Human chr11 - 65605878 65605878 65605878 TTGCTTTCCCCAAGTCCTGAAATTCCTAAAGCACCCCTCCTTGCCCTCCCATCACCAGGAGAAGG TTGCTTTCCCCAAGTCCTGAAATTCCTAAAGCCCCCCTCCTTGCCCTCCCATCACCAGGAGAAGG T G MAP3K11 Ensembl:ENSG00000173327 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65605874..65605959 26863196 MeRIP-seq:(Medium) rs565672149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5343948,Human_RBP_ID_26776424 RMVar_hsa_circ_88825,RMVar_hsa_circ_96634,RMVar_hsa_circ_127176,RMVar_hsa_circ_93686,RMVar_hsa_circ_150719,RMVar_hsa_circ_150721,RMVar_hsa_circ_150722,RMVar_hsa_circ_150720,RMVar_hsa_circ_33691,RMVar_hsa_circ_276446,RMVar_hsa_circ_150723 56937 RMVar_ID_56937 Human_SNP_ID_470076579 m1A Human chr11 - 65605952 65605952 65605952 TCCCAGTTCCCCCAAGCCTGGGGAAGCCCAGAATGGGAGGTGAGTACCTGAGTGCCCCCCAGACC TCCCAGTTCCCCCAAGCCTGGGGAAGCCCAGAGTGGGAGGTGAGTACCTGAGTGCCCCCCAGACC T C MAP3K11 Ensembl:ENSG00000173327 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65599565..65606061 32194978 MeRIP-seq:(Medium) rs1412779351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750421,Human_RBP_ID_808162 Human_Splice_Rec_1259449,Human_Splice_Rec_1259467,Human_Splice_Rec_1259485,Human_Splice_Rec_1259501,Human_Splice_Rec_1259509,Human_Splice_Rec_1259515 RMVar_hsa_circ_88825,RMVar_hsa_circ_96634,RMVar_hsa_circ_127176,RMVar_hsa_circ_93686,RMVar_hsa_circ_150719,RMVar_hsa_circ_150721,RMVar_hsa_circ_150722,RMVar_hsa_circ_150720,RMVar_hsa_circ_33691,RMVar_hsa_circ_276446,RMVar_hsa_circ_111945,RMVar_hsa_circ_150723,RMVar_hsa_circ_7776,RMVar_hsa_circ_150724 56938 RMVar_ID_56938 Human_SNP_ID_470076873 m1A Human chr11 + 65606765 65606765 65606765 GCCCGACCTCGAAGACGTTTCTCCTCCGGTCAAGGCCGGGTGAGGCCTGCACGGTGATGCGGTGC GCCCGACCTCGAAGACGTTTCTCCTCCGGTCATGGCCGGGTGAGGCCTGCACGGTGATGCGGTGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65606695..65606846 32194978 MeRIP-seq:(Medium) rs762853042 Functional Loss SNV dbSNP153 33..33 33 - - - 56939 RMVar_ID_56939 Human_SNP_ID_470077181 m1A Human chr11 - 65607434 65607434 65607434 GCGGTCACAGGCGGAGCAGCTGCGGCGGCGCGAGCACCTGCTGGCCCAGTGGGAGCTAGAGGTGT GCGGTCACAGGCGGAGCAGCTGCGGCGGCGCGCGCACCTGCTGGCCCAGTGGGAGCTAGAGGTGT T G MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65607332..65607709 26863410 MeRIP-seq:(Medium) rs1565144637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750425,Human_RBP_ID_17109139,Human_RBP_ID_27804684 Human_Splice_Rec_1259462,Human_Splice_Rec_1259480,Human_Splice_Rec_1259496,Human_Splice_Rec_1259520,Human_Splice_Rec_1259524 Human_miRNA_ID_1692339,Human_miRNA_ID_2221959,Human_miRNA_ID_2485016,Human_miRNA_ID_2662365,Human_miRNA_ID_2680816,Human_miRNA_ID_2868100,Human_miRNA_ID_3073393 RMVar_hsa_circ_88825,RMVar_hsa_circ_96634,RMVar_hsa_circ_93686,RMVar_hsa_circ_150721,RMVar_hsa_circ_150722,RMVar_hsa_circ_150720,RMVar_hsa_circ_33691,RMVar_hsa_circ_276446,RMVar_hsa_circ_95823,RMVar_hsa_circ_111945,RMVar_hsa_circ_150723,RMVar_hsa_circ_7776,RMVar_hsa_circ_150724,RMVar_hsa_circ_150725 56940 RMVar_ID_56940 Human_SNP_ID_470078779 m1A Human chr11 - 65613398 65613398 65613398 CGAGGTGGCCAGCTTCCAGGAGCTGCGGCTGGAGGAGGTGATCGGCATTGGAGGCTTTGGCAAGG CGAGGTGGCCAGCTTCCAGGAGCTGCGGCTGGGGGAGGTGATCGGCATTGGAGGCTTTGGCAAGG T C MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65613347..65613674 26863196 MeRIP-seq:(Medium) rs200642724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227959,Human_RBP_ID_3939422,Human_RBP_ID_17648796,Human_RBP_ID_22034642,Human_RBP_ID_22709547 56941 RMVar_ID_56941 Human_SNP_ID_470078833 m1A Human chr11 - 65613532 65613532 65613532 GGTGACCGTGTGGAGGTGCTGTCCCGGGACGCAGCCATCTCAGGAGACGAGGGCTGGTGGGCGGG GGTGACCGTGTGGAGGTGCTGTCCCGGGACGCGGCCATCTCAGGAGACGAGGGCTGGTGGGCGGG T C MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65613376..65613575;chr11:65613235..65614286 26863196 MeRIP-seq:(Medium) rs368386691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17109140 56942 RMVar_ID_56942 Human_SNP_ID_470078834 m1A Human chr11 - 65613532 65613532 65613532 GGTGACCGTGTGGAGGTGCTGTCCCGGGACGCAGCCATCTCAGGAGACGAGGGCTGGTGGGCGGG GGTGACCGTGTGGAGGTGCTGTCCCGGGACGCCGCCATCTCAGGAGACGAGGGCTGGTGGGCGGG T G MAP3K11 Ensembl:ENSG00000173327 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65613376..65613575;chr11:65613235..65614286 26863196 MeRIP-seq:(Medium) rs368386691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17109140 56943 RMVar_ID_56943 Human_SNP_ID_470079669 m1A Human chr11 + 65615870 65615870 65615870 ACCAGCAGAAGCCGGGCGAGCGCGGAGCCCCAAGCAAGTGACCTGCGACCCCGAAAGTGGACCCC ACCAGCAGAAGCCGGGCGAGCGCGGAGCCCCACGCAAGTGACCTGCGACCCCGAAAGTGGACCCC A C PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65615842..65615944 26863196 MeRIP-seq:(Medium) rs769182471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185095,Human_RBP_ID_27804685 56944 RMVar_ID_56944 Human_SNP_ID_470079670 m1A Human chr11 + 65615870 65615870 65615870 ACCAGCAGAAGCCGGGCGAGCGCGGAGCCCCAAGCAAGTGACCTGCGACCCCGAAAGTGGACCCC ACCAGCAGAAGCCGGGCGAGCGCGGAGCCCCAGGCAAGTGACCTGCGACCCCGAAAGTGGACCCC A G PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65615842..65615944 26863196 MeRIP-seq:(Medium) rs769182471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185095,Human_RBP_ID_27804685 56945 RMVar_ID_56945 Human_SNP_ID_470079673 m1A Human chr11 + 65615874 65615874 65615874 GCAGAAGCCGGGCGAGCGCGGAGCCCCAAGCAAGTGACCTGCGACCCCGAAAGTGGACCCCAGAT GCAGAAGCCGGGCGAGCGCGGAGCCCCAAGCAGGTGACCTGCGACCCCGAAAGTGGACCCCAGAT A G PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65615826..65616050;chr11:65615826..65616000;chr11:65615850..65616036 26863196 MeRIP-seq:(Medium) rs1037138677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185095,Human_RBP_ID_27804685 56946 RMVar_ID_56946 Human_SNP_ID_470079702 m1A Human chr11 + 65615962 65615962 65615962 GACTAGGGAGCTGTCGCCTGCACCCCGGGAGCACCCACCCCACGACCACCTCTGGATGCCGCCGA GACTAGGGAGCTGTCGCCTGCACCCCGGGAGCCCCCACCCCACGACCACCTCTGGATGCCGCCGA A C PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65615826..65616025 26863196 MeRIP-seq:(Medium) rs1360135694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185096 56947 RMVar_ID_56947 Human_SNP_ID_470079724 m1A Human chr11 + 65616048 65616048 65616048 GCGCCTGCCTGCCGGCTCGGCCCCTCGGAGCAATTCTGGGCCAGGAGTGGGGACCCGGACCCCGC GCGCCTGCCTGCCGGCTCGGCCCCTCGGAGCACTTCTGGGCCAGGAGTGGGGACCCGGACCCCGC A C PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65615860..65616062 26863410 MeRIP-seq:(Medium) rs1167850096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186023,Human_RBP_ID_5460665,Human_RBP_ID_5520783,Human_RBP_ID_22165005,Human_RBP_ID_22433757 56948 RMVar_ID_56948 Human_SNP_ID_470079725 m1A Human chr11 + 65616048 65616048 65616048 GCGCCTGCCTGCCGGCTCGGCCCCTCGGAGCAATTCTGGGCCAGGAGTGGGGACCCGGACCCCGC GCGCCTGCCTGCCGGCTCGGCCCCTCGGAGCAGTTCTGGGCCAGGAGTGGGGACCCGGACCCCGC A G PCNX3 Ensembl:ENSG00000197136 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65615860..65616062 26863410 MeRIP-seq:(Medium) rs1167850096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186023,Human_RBP_ID_5460665,Human_RBP_ID_5520783,Human_RBP_ID_22165005,Human_RBP_ID_22433757 56949 RMVar_ID_56949 Human_SNP_ID_470081164 m1A Human chr11 - 65618915 65618915 65618915 CCTGGGCCTCCAGCTCTGCCTTGCAGCCAGCCAGTGGGGGCCTCAGAACATCACCCCCAGCCCCA CCTGGGCCTCCAGCTCTGCCTTGCAGCCAGCCTGTGGGGGCCTCAGAACATCACCCCCAGCCCCA T A L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65618866..65619016 32194978 MeRIP-seq:(Medium) rs759804910 Functional Loss SNV dbSNP153 33..33 33 - - - 56950 RMVar_ID_56950 Human_SNP_ID_470081165 m1A Human chr11 - 65618915 65618915 65618915 CCTGGGCCTCCAGCTCTGCCTTGCAGCCAGCCAGTGGGGGCCTCAGAACATCACCCCCAGCCCCA CCTGGGCCTCCAGCTCTGCCTTGCAGCCAGCCGGTGGGGGCCTCAGAACATCACCCCCAGCCCCA T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65618866..65619016 32194978 MeRIP-seq:(Medium) rs759804910 Functional Loss SNV dbSNP153 33..33 33 - - - 56951 RMVar_ID_56951 Human_SNP_ID_470081214 m1A Human chr11 + 65619038 65619038 65619038 ACCCGCTGCCAACCAGCCCGGCTGGCGGGGGGAGCTGCAGGAGGAAGGTGCTGTGGGGGGAGGTG ACCCGCTGCCAACCAGCCCGGCTGGCGGGGGGGGCTGCAGGAGGAAGGTGCTGTGGGGGGAGGTG A G PCNX3 Ensembl:ENSG00000197136 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65618988..65619080 26863196 MeRIP-seq:(Medium) rs929677992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3047,Human_RBP_ID_5520791,Human_RBP_ID_22433759,Human_RBP_ID_22708869,Human_RBP_ID_24550958 Human_Splice_Rec_1259549 Human_miRNA_ID_2012892,Human_miRNA_ID_2759274 RMVar_hsa_circ_109899,RMVar_hsa_circ_75807,RMVar_hsa_circ_85381,RMVar_hsa_circ_77819,RMVar_hsa_circ_117520,RMVar_hsa_circ_150728,RMVar_hsa_circ_150727,RMVar_hsa_circ_108372,RMVar_hsa_circ_150730,RMVar_hsa_circ_150731,RMVar_hsa_circ_150732,RMVar_hsa_circ_118007,RMVar_hsa_circ_80725,RMVar_hsa_circ_98050,RMVar_hsa_circ_80041,RMVar_hsa_circ_150735,RMVar_hsa_circ_150736,RMVar_hsa_circ_150734,RMVar_hsa_circ_102962,RMVar_hsa_circ_112594,RMVar_hsa_circ_150738,RMVar_hsa_circ_93720,RMVar_hsa_circ_150739,RMVar_hsa_circ_150737,RMVar_hsa_circ_120164,RMVar_hsa_circ_150741,RMVar_hsa_circ_88504,RMVar_hsa_circ_150740,RMVar_hsa_circ_340900,RMVar_hsa_circ_87089,RMVar_hsa_circ_116942,RMVar_hsa_circ_81100,RMVar_hsa_circ_150743,RMVar_hsa_circ_150745,RMVar_hsa_circ_150746,RMVar_hsa_circ_150747,RMVar_hsa_circ_150744,RMVar_hsa_circ_150742 56952 RMVar_ID_56952 Human_SNP_ID_470083836 m1A Human chr11 + 65625665 65625665 65625665 GTCTCTCCTGGCCCTGCAGCGTGAGGTCTTGCACTCCGACCTGGTGATGTGTGTGGTGATCGCCG GTCTCTCCTGGCCCTGCAGCGTGAGGTCTTGCGCTCCGACCTGGTGATGTGTGTGGTGATCGCCG A G PCNX3 Ensembl:ENSG00000197136 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65624553..65626128 32194978 MeRIP-seq:(Medium) rs1269554344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939440,Human_RBP_ID_5345656,Human_RBP_ID_8771015,Human_RBP_ID_9276543,Human_RBP_ID_18972286 Human_Splice_Rec_1259574,Human_Splice_Rec_1259575,Human_Splice_Rec_1259614,Human_Splice_Rec_1259615 Human_miRNA_ID_2019546,Human_miRNA_ID_2024641,Human_miRNA_ID_2311261,Human_miRNA_ID_2313279,Human_miRNA_ID_2499372,Human_miRNA_ID_2607157,Human_miRNA_ID_2655063 RMVar_hsa_circ_118007,RMVar_hsa_circ_80041,RMVar_hsa_circ_150735,RMVar_hsa_circ_150736,RMVar_hsa_circ_102962,RMVar_hsa_circ_112594,RMVar_hsa_circ_150738,RMVar_hsa_circ_150739,RMVar_hsa_circ_120164,RMVar_hsa_circ_101027,RMVar_hsa_circ_150747,RMVar_hsa_circ_84844,RMVar_hsa_circ_150751,RMVar_hsa_circ_109891,RMVar_hsa_circ_91036,RMVar_hsa_circ_93012,RMVar_hsa_circ_150753,RMVar_hsa_circ_86636,RMVar_hsa_circ_150754,RMVar_hsa_circ_150755,RMVar_hsa_circ_150756,RMVar_hsa_circ_150757,RMVar_hsa_circ_85541,RMVar_hsa_circ_150758 56953 RMVar_ID_56953 Human_SNP_ID_470088870 m1A Human chr11 + 65640949 65640949 65640949 AGAGCATGCCCATGTGGGCCGGCGGTGTGGGGAGCCCTCGGCGGGGCATGGCCCCTGCGTCCACA AGAGCATGCCCATGTGGGCCGGCGGTGTGGGGTGCCCTCGGCGGGGCATGGCCCCTGCGTCCACA A T SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65640812..65641159 26863196 MeRIP-seq:(Medium) rs765175393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184228,Human_RBP_ID_5235073,Human_RBP_ID_17799281,Human_RBP_ID_21966594,Human_RBP_ID_22034653 56954 RMVar_ID_56954 Human_SNP_ID_470089375 m1A Human chr11 + 65642348 65642348 65642348 AGAAGGAGGGCAGCGGAGGGGGCACCCTGCACAGCTACCGCGTCATCGTGCGGACCACGCAGGTG AGAAGGAGGGCAGCGGAGGGGGCACCCTGCACCGCTACCGCGTCATCGTGCGGACCACGCAGGTG A C SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65642298..65642646 26863196 MeRIP-seq:(Medium) rs950211371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866674,Human_RBP_ID_3939451 Human_Splice_Rec_1259650,Human_Splice_Rec_1259651,Human_Splice_Rec_1259686,Human_Splice_Rec_1259687,Human_Splice_Rec_1259718,Human_Splice_Rec_1259719,Human_Splice_Rec_1259745 56955 RMVar_ID_56955 Human_SNP_ID_470091609 m1A Human chr11 + 65649396 65649396 65649396 CACAAAGCAGCTGCTGCACCTGTGCCTGCAAGATGGTGGCAGTCCTCCAGGGCCTGGGGATCTGG CACAAAGCAGCTGCTGCACCTGTGCCTGCAAGGTGGTGGCAGTCCTCCAGGGCCTGGGGATCTGG A G SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65649345..65649688 32194978 MeRIP-seq:(Medium) rs139438277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1259665,Human_Splice_Rec_1259703,Human_Splice_Rec_1259733 RMVar_hsa_circ_17005 56956 RMVar_ID_56956 Human_SNP_ID_470091643 m1A Human chr11 + 65649479 65649479 65649479 TCCTGCACAGCCAGAACTCGCTGTCACCACGCAGGTGCACACTCTTGGCCTTCCCTCTCCTCCAG TCCTGCACAGCCAGAACTCGCTGTCACCACGCCGGTGCACACTCTTGGCCTTCCCTCTCCTCCAG A C SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65649472..65649571 26863196 MeRIP-seq:(Medium) rs1222107321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1259665,Human_Splice_Rec_1259703,Human_Splice_Rec_1259733 RMVar_hsa_circ_17005 56957 RMVar_ID_56957 Human_SNP_ID_470091644 m1A Human chr11 + 65649479 65649479 65649479 TCCTGCACAGCCAGAACTCGCTGTCACCACGCAGGTGCACACTCTTGGCCTTCCCTCTCCTCCAG TCCTGCACAGCCAGAACTCGCTGTCACCACGCGGGTGCACACTCTTGGCCTTCCCTCTCCTCCAG A G SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65649472..65649571 26863196 MeRIP-seq:(Medium) rs1222107321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1259665,Human_Splice_Rec_1259703,Human_Splice_Rec_1259733 RMVar_hsa_circ_17005 56958 RMVar_ID_56958 Human_SNP_ID_470093810 m1A Human chr11 - 65655730 65655730 65655730 GACCCACCGACCCCCGGCCTCCACCTCGACGCATTGCTGTGCCTTCCCGCAGCTCAGCTTCTGTC GACCCACCGACCCCCGGCCTCCACCTCGACGCGTTGCTGTGCCTTCCCGCAGCTCAGCTTCTGTC T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65655681..65655873 32194978 MeRIP-seq:(Medium) rs1180352560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750402,Human_RBP_ID_3939455,Human_RBP_ID_4172596,Human_RBP_ID_18933701 Human_Splice_Rec_1259785,Human_Splice_Rec_1259804,Human_Splice_Rec_1259805,Human_Splice_Rec_1259824,Human_Splice_Rec_1259842,Human_Splice_Rec_1259843,Human_Splice_Rec_1259862,Human_Splice_Rec_1259863,Human_Splice_Rec_1259882,Human_Splice_Rec_1259883,Human_Splice_Rec_1259900,Human_Splice_Rec_1259901,Human_Splice_Rec_1259920,Human_Splice_Rec_1259921,Human_Splice_Rec_1259926 Human_miRNA_ID_102985,Human_miRNA_ID_1494099,Human_miRNA_ID_1964305,Human_miRNA_ID_2763755,Human_miRNA_ID_2932135 RMVar_hsa_circ_48521,RMVar_hsa_circ_109572,RMVar_hsa_circ_336384,RMVar_hsa_circ_150771,RMVar_hsa_circ_336053 56959 RMVar_ID_56959 Human_SNP_ID_470093815 m1A Human chr11 + 65655737 65655737 65655737 GCTGAGCTGCGGGAAGGCACAGCAATGCGTCGAGGTGGAGGCCGGGGGTCGGTGGGTCCTGTAGG GCTGAGCTGCGGGAAGGCACAGCAATGCGTCGGGGTGGAGGCCGGGGGTCGGTGGGTCCTGTAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:65655625..65655972;chr11:65655676..65655873;chr11:65655676..65655923 26863196 MeRIP-seq:(Medium) rs781482288 Functional Loss SNV dbSNP153 33..33 33 - - - 56960 RMVar_ID_56960 Human_SNP_ID_470094565 m1A Human chr11 - 65658388 65658388 65658388 GGCCATTGTGTTCCGGACCCCTCCCTACGCAGACCCCAGCCTGCAGGCTCCTGTGCGTGTCTCCA GGCCATTGTGTTCCGGACCCCTCCCTACGCAGGCCCCAGCCTGCAGGCTCCTGTGCGTGTCTCCA T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65658276..65658425 26863196 MeRIP-seq:(Medium) rs745468574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109749,Human_RBP_ID_400980,Human_RBP_ID_27804688 RMVar_hsa_circ_48521,RMVar_hsa_circ_109572,RMVar_hsa_circ_336384,RMVar_hsa_circ_150771,RMVar_hsa_circ_336053,RMVar_hsa_circ_49292 56961 RMVar_ID_56961 Human_SNP_ID_470095130 m1A Human chr11 - 65660289 65660289 65660289 GGAGCGATGATCTAGGGGTGGGCAGAGTAGGAAGGAGCAGGCTGGGCAAGGCAGGAAGGTCTGGG GGAGCGATGATCTAGGGGTGGGCAGAGTAGGATGGAGCAGGCTGGGCAAGGCAGGAAGGTCTGGG T A RELA Ensembl:ENSG00000173039 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65660221..65660712 26863196 MeRIP-seq:(Medium) rs1565191552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939456,Human_RBP_ID_5343984 56962 RMVar_ID_56962 Human_SNP_ID_470095662 m1A Human chr11 - 65662090 65662090 65662090 AGCCGCCTAATGGGGCTGCGGTGTCCCCTGGCAGAGCCAGCCCAGGCCTCTGGCCCCTATGTGGA AGCCGCCTAATGGGGCTGCGGTGTCCCCTGGCGGAGCCAGCCCAGGCCTCTGGCCCCTATGTGGA T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65662076..65662225 26863196 MeRIP-seq:(Medium) rs1244040029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865241,Human_RBP_ID_5342675,Human_RBP_ID_18974178,Human_RBP_ID_19049899,Human_RBP_ID_22537605,Human_RBP_ID_26776449 56963 RMVar_ID_56963 Human_SNP_ID_470095956 m1A Human chr11 + 65662884 65662884 65662884 GGGCCGGGGTCGCAGCTGGGCCCGCGGCGTGCACTACAGACGAGCCATTCGCCAGAGGCGGAAAT GGGCCGGGGTCGCAGCTGGGCCCGCGGCGTGCGCTACAGACGAGCCATTCGCCAGAGGCGGAAAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65662771..65662925 26863196 MeRIP-seq:(Medium) rs1389560079 Functional Loss SNV dbSNP153 33..33 33 - - - 56964 RMVar_ID_56964 Human_SNP_ID_470096013 m1A Human chr11 + 65663043 65663043 65663043 CACGCCGCGCGGAGGACGAAGAGGCTGCACGCACAGCCGCTGCCGGGGGTCGGGGCCAAGTGCGC CACGCCGCGCGGAGGACGAAGAGGCTGCACGCCCAGCCGCTGCCGGGGGTCGGGGCCAAGTGCGC A C RELA-DT Ensembl:ENSG00000285533 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65662994..65663094 26863196 MeRIP-seq:(Medium) rs1013951771 Functional Loss SNV dbSNP153 33..33 33 - - - 56965 RMVar_ID_56965 Human_SNP_ID_470108305 m1A Human chr11 - 65712290 65712290 65712290 CCTCCCCTGGCTCCCTCCGCCCCGCCCCGGGCACCGGACTCACCACCTCCGCCATCTTCCCTCCC CCTCCCCTGGCTCCCTCCGCCCCGCCCCGGGCGCCGGACTCACCACCTCCGCCATCTTCCCTCCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65712251..65712450 26863196 MeRIP-seq:(Medium) rs1430838182 Functional Loss SNV dbSNP153 33..33 33 - - - 56966 RMVar_ID_56966 Human_SNP_ID_470108377 m1A Human chr11 + 65712405 65712405 65712405 CCCCAGGGGGAGATAATCGAGGGCTGCCGCCTACCCGTGCTGCGGCGGAACCAGGACAACGAAGA CCCCAGGGGGAGATAATCGAGGGCTGCCGCCTGCCCGTGCTGCGGCGGAACCAGGACAACGAAGA A G KAT5 Ensembl:ENSG00000172977 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:65712293..65712444 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_227060,Human_RBP_ID_400989,Human_RBP_ID_865975,Human_RBP_ID_3940838,Human_RBP_ID_4186034,Human_RBP_ID_18417184,Human_RBP_ID_18974180,Human_RBP_ID_22435464,Human_RBP_ID_26318748 Human_Splice_Rec_1260090,Human_Splice_Rec_1260091,Human_Splice_Rec_1260116,Human_Splice_Rec_1260117,Human_Splice_Rec_1260140,Human_Splice_Rec_1260141,Human_Splice_Rec_1260145,Human_Splice_Rec_1260168,Human_Splice_Rec_1260169,Human_Splice_Rec_1260179,Human_Splice_Rec_1260203,Human_Splice_Rec_1260211,Human_Splice_Rec_1260223 RMVar_hsa_circ_79413,RMVar_hsa_circ_150772 56967 RMVar_ID_56967 Human_SNP_ID_470108387 m1A Human chr11 - 65712447 65712447 65712447 AGGTTCCTTAGTCCCGCCCCCCAACGTCACTCACGCCACTCATCTTCGTTGTCCTGGTTCCGCCG AGGTTCCTTAGTCCCGCCCCCCAACGTCACTCGCGCCACTCATCTTCGTTGTCCTGGTTCCGCCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr11:65712251..65712475;chr11:65712251..65712450 26863410 MeRIP-seq:(Medium) rs1437666030 Functional Loss SNV dbSNP153 33..33 33 - - - 56968 RMVar_ID_56968 Human_SNP_ID_470109221 m1A Human chr11 - 65714607 65714607 65714607 ACCACGGCTTGAGGCGGTGCCGGCCCAGCTCAATGCACTCAATGTTCTTCATCCGGGTGACGATG ACCACGGCTTGAGGCGGTGCCGGCCCAGCTCAGTGCACTCAATGTTCTTCATCCGGGTGACGATG T C RNASEH2C Ensembl:ENSG00000172922 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65714560..65714631 26863196 MeRIP-seq:(Medium) rs570448126 Functional Loss SNV dbSNP153 33..33 33 - - - 56969 RMVar_ID_56969 Human_SNP_ID_470110702 m1A Human chr11 + 65719489 65719489 65719489 CGGATGGGGGAGCTCTGTACAGAGGGCTGGTGATTGTAAAAATTTCTTTTGTAAAGTAGAAGTTG CGGATGGGGGAGCTCTGTACAGAGGGCTGGTGGTTGTAAAAATTTCTTTTGTAAAGTAGAAGTTG A G KAT5 Ensembl:ENSG00000172977 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65719454..65719604 32194978 MeRIP-seq:(Medium) rs898565080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17799326,Human_RBP_ID_21883062,Human_RBP_ID_26408706 Human_miRNA_ID_497180 56970 RMVar_ID_56970 Human_SNP_ID_470110810 m1A Human chr11 - 65719783 65719783 65719783 TTGCAGATTCACGCACAGGTGCCCGAGGACTGAGAACCAGAGCTTGAAATTCAAAGCTGCGATCC TTGCAGATTCACGCACAGGTGCCCGAGGACTGGGAACCAGAGCTTGAAATTCAAAGCTGCGATCC T C RNASEH2C Ensembl:ENSG00000172922 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65719701..65719825 32194978 MeRIP-seq:(Medium) rs749473518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401025,Human_RBP_ID_1354891,Human_RBP_ID_1459343,Human_RBP_ID_1781541,Human_RBP_ID_5170265,Human_RBP_ID_6086461,Human_RBP_ID_11675059,Human_RBP_ID_17649170,Human_RBP_ID_27414575 Human_Splice_Rec_1260302,Human_Splice_Rec_1260308,Human_Splice_Rec_1260322,Human_Splice_Rec_1260330,Human_Splice_Rec_1260332,Human_Splice_Rec_1260338,Human_Splice_Rec_1260344,Human_Splice_Rec_1260350,Human_Splice_Rec_1260356,Human_Splice_Rec_1260362 RMVar_hsa_circ_98913,RMVar_hsa_circ_150774 56971 RMVar_ID_56971 Human_SNP_ID_470110811 m1A Human chr11 - 65719783 65719783 65719783 TTGCAGATTCACGCACAGGTGCCCGAGGACTGAGAACCAGAGCTTGAAATTCAAAGCTGCGATCC TTGCAGATTCACGCACAGGTGCCCGAGGACTGCGAACCAGAGCTTGAAATTCAAAGCTGCGATCC T G RNASEH2C Ensembl:ENSG00000172922 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65719701..65719825 32194978 MeRIP-seq:(Medium) rs749473518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401025,Human_RBP_ID_1354891,Human_RBP_ID_1459343,Human_RBP_ID_1781541,Human_RBP_ID_5170265,Human_RBP_ID_6086461,Human_RBP_ID_11675059,Human_RBP_ID_17649170,Human_RBP_ID_27414575 Human_Splice_Rec_1260302,Human_Splice_Rec_1260308,Human_Splice_Rec_1260322,Human_Splice_Rec_1260330,Human_Splice_Rec_1260332,Human_Splice_Rec_1260338,Human_Splice_Rec_1260344,Human_Splice_Rec_1260350,Human_Splice_Rec_1260356,Human_Splice_Rec_1260362 RMVar_hsa_circ_98913,RMVar_hsa_circ_150774 56972 RMVar_ID_56972 Human_SNP_ID_470111113 m1A Human chr11 - 65720313 65720313 65720313 ACGTGATGGTGACAGAAGAGAAGAAGGTGTCGATGGGGAAGCCAGACCCCTTGCGGGATTCCGGG ACGTGATGGTGACAGAAGAGAAGAAGGTGTCGTTGGGGAAGCCAGACCCCTTGCGGGATTCCGGG T A RNASEH2C Ensembl:ENSG00000172922 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:65720251..65720479;chr11:65720255..65720465 26863196 MeRIP-seq:(Medium) rs749085392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809142,Human_RBP_ID_4193436,Human_RBP_ID_5550037,Human_RBP_ID_9321584,Human_RBP_ID_9362514,Human_RBP_ID_17649172,Human_RBP_ID_18611112,Human_RBP_ID_18974184,Human_RBP_ID_26320199,Human_RBP_ID_27804693 Human_Splice_Rec_1260299,Human_Splice_Rec_1260305,Human_Splice_Rec_1260319,Human_Splice_Rec_1260327,Human_Splice_Rec_1260335,Human_Splice_Rec_1260341,Human_Splice_Rec_1260347,Human_Splice_Rec_1260353,Human_Splice_Rec_1260359,Human_Splice_Rec_1260367 RMVar_hsa_circ_98913,RMVar_hsa_circ_150774 56973 RMVar_ID_56973 Human_SNP_ID_470111341 m1A Human chr11 + 65720698 65720674 65720698 CAGATGCAGTGTGGCGGGTACGGCGTCGCGCAATGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT CAGATGCAG________________________TGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT GTGTGGCGGGTACGGCGTCGCGCAA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65720576..65720800 26863410 MeRIP-seq:(Medium) rs1565213769 Functional Loss DEL dbSNP153 10..33 33 - - - 56974 RMVar_ID_56974 Human_SNP_ID_470111357 m1A Human chr11 + 65720698 65720698 65720698 CAGATGCAGTGTGGCGGGTACGGCGTCGCGCAATGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT CAGATGCAGTGTGGCGGGTACGGCGTCGCGCAGTGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65720576..65720800 26863410 MeRIP-seq:(Medium) rs376140250 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_158 56975 RMVar_ID_56975 Human_SNP_ID_470111358 m1A Human chr11 + 65720698 65720698 65720698 CAGATGCAGTGTGGCGGGTACGGCGTCGCGCAATGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT CAGATGCAGTGTGGCGGGTACGGCGTCGCGCATTGTGGCGGAGCGCAAGTGGACGCGGTGCCTCT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65720576..65720800 26863410 MeRIP-seq:(Medium) rs376140250 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_158 56976 RMVar_ID_56976 Human_SNP_ID_470111390 m1A Human chr11 - 65720761 65720758 65720762 CAGCTCGCGAGCCCTGGCGTCGCGTAGGAGGGAGGATGGAGAGCGGCGACGAAGCGGCCATCGAG CAGCTCGCGAGCCCTGGCGTCGCGTAGGAGG____ATGGAGAGCGGCGACGAAGCGGCCATCGAG TCCTC T RNASEH2C Ensembl:ENSG00000172922 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65720554..65720800 26863196 MeRIP-seq:(Medium) rs1333471827 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_751575,Human_RBP_ID_4185104 56977 RMVar_ID_56977 Human_SNP_ID_470111393 m1A Human chr11 - 65720761 65720761 65720761 CAGCTCGCGAGCCCTGGCGTCGCGTAGGAGGGAGGATGGAGAGCGGCGACGAAGCGGCCATCGAG CAGCTCGCGAGCCCTGGCGTCGCGTAGGAGGGGGGATGGAGAGCGGCGACGAAGCGGCCATCGAG T C RNASEH2C Ensembl:ENSG00000172922 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65720554..65720800 26863196 MeRIP-seq:(Medium) rs1280435007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751575,Human_RBP_ID_4185104 56978 RMVar_ID_56978 Human_SNP_ID_470125319 m1A Human chr11 - 65778285 65778285 65778285 CTGCCTCTGCAGCCCCGATGCCCGGCCCCCGCACGGCTGGATGTCCATGCCCTTTACACCACATC CTGCCTCTGCAGCCCCGATGCCCGGCCCCCGCGCGGCTGGATGTCCATGCCCTTTACACCACATC T C AP5B1 Ensembl:ENSG00000254470 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65778242..65778400 26863196 MeRIP-seq:(Medium) rs533899858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092944,Human_RBP_ID_5235247,Human_RBP_ID_9254895,Human_RBP_ID_17235424,Human_RBP_ID_27205274 Human_miRNA_ID_1863732,Human_miRNA_ID_1895225,Human_miRNA_ID_1901113,Human_miRNA_ID_1903751 56979 RMVar_ID_56979 Human_SNP_ID_470126066 m1A Human chr11 - 65779657 65779657 65779657 GGCTGCGGTGATCCAGCTTCTGGACACCTCCTATCTGCTCACTCCTGTGGCCCAGGCCCAGCTCC GGCTGCGGTGATCCAGCTTCTGGACACCTCCTGTCTGCTCACTCCTGTGGCCCAGGCCCAGCTCC T C AP5B1 Ensembl:ENSG00000254470 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65779611..65779860 32194978 MeRIP-seq:(Medium) rs1565225768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401044,Human_RBP_ID_3939459,Human_RBP_ID_4193450,Human_RBP_ID_17672991,Human_RBP_ID_22033009,Human_RBP_ID_27414654 56980 RMVar_ID_56980 Human_SNP_ID_470126389 m1A Human chr11 - 65780238 65780238 65780238 GCCACCTCCCTGTTGGACACCTTGGTCCTCCTACCCCCGCGGCCCTCAGCTCTCCGTCGGCCACT GCCACCTCCCTGTTGGACACCTTGGTCCTCCTCCCCCCGCGGCCCTCAGCTCTCCGTCGGCCACT T G AP5B1 Ensembl:ENSG00000254470 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65780187..65780261 26863196 MeRIP-seq:(Medium) rs757254291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22034680,Human_RBP_ID_27414662 56981 RMVar_ID_56981 Human_SNP_ID_470126618 m1A Human chr11 - 65780708 65780697 65780708 CACCGTGGGAGCCGGGCGCGGGTCCCGCCGGCATCTGCGCGGCGTCTGGGGGTGACCGCAGCCCC CACCGTGGGAGCCGGGCGCGGGTCCCGCCGGC___________GTCTGGGGGTGACCGCAGCCCC CGCCGCGCAGAT C AP5B1 Ensembl:ENSG00000254470 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65780662..65780938 26863196 MeRIP-seq:(Medium) rs1224744647 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_751807,Human_RBP_ID_4172803,Human_RBP_ID_5166662,Human_RBP_ID_17799347 56982 RMVar_ID_56982 Human_SNP_ID_470126622 m1A Human chr11 - 65780708 65780708 65780708 CACCGTGGGAGCCGGGCGCGGGTCCCGCCGGCATCTGCGCGGCGTCTGGGGGTGACCGCAGCCCC CACCGTGGGAGCCGGGCGCGGGTCCCGCCGGCGTCTGCGCGGCGTCTGGGGGTGACCGCAGCCCC T C AP5B1 Ensembl:ENSG00000254470 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65780662..65780938 26863196 MeRIP-seq:(Medium) rs528636119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751807,Human_RBP_ID_4172803,Human_RBP_ID_5166662,Human_RBP_ID_17799347 56983 RMVar_ID_56983 Human_SNP_ID_470146788 m1A Human chr11 - 65855029 65855029 65855029 GGGGAGCCTGTATTTTTTTTAACAACATCCCCATTCCCCACCTGGTCCTCCCCCTTCCCATGCTG GGGGAGCCTGTATTTTTTTTAACAACATCCCCGTTCCCCACCTGGTCCTCCCCCTTCCCATGCTG T C CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65854980..65855328 26863196 MeRIP-seq:(Medium) rs1370724100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31458,Human_RBP_ID_227039,Human_RBP_ID_401057,Human_RBP_ID_808461,Human_RBP_ID_871332,Human_RBP_ID_1265415,Human_RBP_ID_1354895,Human_RBP_ID_1781548,Human_RBP_ID_3378211,Human_RBP_ID_4193463,Human_RBP_ID_5126654,Human_RBP_ID_5139376,Human_RBP_ID_5490106,Human_RBP_ID_6086552,Human_RBP_ID_8062118,Human_RBP_ID_8356135,Human_RBP_ID_11675410,Human_RBP_ID_16987192,Human_RBP_ID_17073747,Human_RBP_ID_17232867,Human_RBP_ID_17349180,Human_RBP_ID_17465809,Human_RBP_ID_17560651,Human_RBP_ID_17649175,Human_RBP_ID_17682434,Human_RBP_ID_17799360,Human_RBP_ID_18198752,Human_RBP_ID_18205881,Human_RBP_ID_18932612,Human_RBP_ID_22791850,Human_RBP_ID_23515547,Human_RBP_ID_24404341,Human_RBP_ID_24463408,Human_RBP_ID_26747692,Human_RBP_ID_26894966,Human_RBP_ID_27205310,Human_RBP_ID_27414668 Human_miRNA_ID_551444,Human_miRNA_ID_2725813 RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_101711,RMVar_hsa_circ_104789,RMVar_hsa_circ_150783,RMVar_hsa_circ_94924,RMVar_hsa_circ_150782,RMVar_hsa_circ_150780 56984 RMVar_ID_56984 Human_SNP_ID_470146802 m1A Human chr11 + 65855053 65855053 65855053 GTGGGGAATGGGGATGTTGTTAAAAAAAATACAGGCTCCCCCACAACTGGGGTGCCTGGGGGGAA GTGGGGAATGGGGATGTTGTTAAAAAAAATACCGGCTCCCCCACAACTGGGGTGCCTGGGGGGAA A C SNX32 Ensembl:ENSG00000172803 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65855003..65855369 26863196 MeRIP-seq:(Medium) rs1311964476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150784 56985 RMVar_ID_56985 Human_SNP_ID_470146814 m1A Human chr11 - 65855077 65855077 65855077 CCTCTTGGGCTGAAGCAGACCAAGTTCCCCCCAGGCACCCCAGTTGTGGGGGAGCCTGTATTTTT CCTCTTGGGCTGAAGCAGACCAAGTTCCCCCCTGGCACCCCAGTTGTGGGGGAGCCTGTATTTTT T A CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65855026..65855450 32194978 MeRIP-seq:(Medium) rs911280432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227040,Human_RBP_ID_401057,Human_RBP_ID_871333,Human_RBP_ID_1163069,Human_RBP_ID_1354896,Human_RBP_ID_1459360,Human_RBP_ID_1781549,Human_RBP_ID_4193465,Human_RBP_ID_5110519,Human_RBP_ID_6086556,Human_RBP_ID_8356136,Human_RBP_ID_9005527,Human_RBP_ID_11675419,Human_RBP_ID_17466991,Human_RBP_ID_17649176,Human_RBP_ID_18251677,Human_RBP_ID_18933707,Human_RBP_ID_19659913,Human_RBP_ID_22791851,Human_RBP_ID_23207359,Human_RBP_ID_23515548,Human_RBP_ID_24404343,Human_RBP_ID_24463410,Human_RBP_ID_26406005,Human_RBP_ID_26894968,Human_RBP_ID_27205310,Human_RBP_ID_27414674 RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_101711,RMVar_hsa_circ_104789,RMVar_hsa_circ_150783,RMVar_hsa_circ_94924,RMVar_hsa_circ_150782,RMVar_hsa_circ_150780 56986 RMVar_ID_56986 Human_SNP_ID_470146825 m1A Human chr11 - 65855093 65855093 65855093 TTTTGATCTTTTGATTCCTCTTGGGCTGAAGCAGACCAAGTTCCCCCCAGGCACCCCAGTTGTGG TTTTGATCTTTTGATTCCTCTTGGGCTGAAGCTGACCAAGTTCCCCCCAGGCACCCCAGTTGTGG T A CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65854826..65855492 32194978 MeRIP-seq:(Medium) rs766063563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401057,Human_RBP_ID_871333,Human_RBP_ID_1080649,Human_RBP_ID_1354896,Human_RBP_ID_1459360,Human_RBP_ID_1781549,Human_RBP_ID_2276408,Human_RBP_ID_3378212,Human_RBP_ID_5110519,Human_RBP_ID_6086556,Human_RBP_ID_8356136,Human_RBP_ID_9005527,Human_RBP_ID_11675419,Human_RBP_ID_17232869,Human_RBP_ID_17466991,Human_RBP_ID_17560652,Human_RBP_ID_17649176,Human_RBP_ID_18251677,Human_RBP_ID_18933707,Human_RBP_ID_19583119,Human_RBP_ID_22491624,Human_RBP_ID_22791851,Human_RBP_ID_23207000,Human_RBP_ID_23515548,Human_RBP_ID_24404344,Human_RBP_ID_24461948,Human_RBP_ID_26406006,Human_RBP_ID_27205310,Human_RBP_ID_27414674 Human_miRNA_ID_1008531,Human_miRNA_ID_2945683 RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_101711,RMVar_hsa_circ_104789,RMVar_hsa_circ_150783,RMVar_hsa_circ_94924,RMVar_hsa_circ_150782,RMVar_hsa_circ_150780 56987 RMVar_ID_56987 Human_SNP_ID_470146931 m1A Human chr11 - 65855429 65855429 65855429 TTCTTCTTTATAGGGATCAAGCATGAATTGCAAGCAAACTGCTACGAGGAGGTCAAGGACCGCTG TTCTTCTTTATAGGGATCAAGCATGAATTGCAGGCAAACTGCTACGAGGAGGTCAAGGACCGCTG T C CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65854897..65855469 26863196 MeRIP-seq:(Medium) rs756543435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401072,Human_RBP_ID_866681,Human_RBP_ID_1781552,Human_RBP_ID_11675435,Human_RBP_ID_17648800,Human_RBP_ID_22433761,Human_RBP_ID_23515573,Human_RBP_ID_26318754 Human_Splice_Rec_1260410,Human_Splice_Rec_1260418,Human_Splice_Rec_1260426,Human_Splice_Rec_1260432,Human_Splice_Rec_1260436,Human_Splice_Rec_1260442,Human_Splice_Rec_1260448,Human_Splice_Rec_1260456,Human_Splice_Rec_1260460 RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_101711,RMVar_hsa_circ_104789,RMVar_hsa_circ_150783,RMVar_hsa_circ_94924,RMVar_hsa_circ_150782,RMVar_hsa_circ_150780,RMVar_hsa_circ_150785,RMVar_hsa_circ_378623 56988 RMVar_ID_56988 Human_SNP_ID_470147045 m1A Human chr11 - 65855732 65855732 65855732 TGCTGGGAGTTGCCTGACGCGTGTTTCTGTCCAGGGCCCCCGAGTCTGCGCCCCTTAAGAGCAAA TGCTGGGAGTTGCCTGACGCGTGTTTCTGTCCTGGGCCCCCGAGTCTGCGCCCCTTAAGAGCAAA T A CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65855701..65855750 26863196 MeRIP-seq:(Medium) rs1482960648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31463,Human_RBP_ID_871336,Human_RBP_ID_4172831,Human_RBP_ID_22471250,Human_RBP_ID_26894979 Human_Splice_Rec_1260409,Human_Splice_Rec_1260417,Human_Splice_Rec_1260425,Human_Splice_Rec_1260431,Human_Splice_Rec_1260435,Human_Splice_Rec_1260441,Human_Splice_Rec_1260447,Human_Splice_Rec_1260455,Human_Splice_Rec_1260459 RMVar_hsa_circ_352,RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_94924,RMVar_hsa_circ_150780,RMVar_hsa_circ_150785,RMVar_hsa_circ_378623 56989 RMVar_ID_56989 Human_SNP_ID_470147193 m1A Human chr11 - 65856168 65856168 65856168 AACGACATGAAGGTGCGTAAGTCTTCAACGCCAGAGGAGGTGAAGAAGCGCAAGAAGGCGGTGCT AACGACATGAAGGTGCGTAAGTCTTCAACGCCTGAGGAGGTGAAGAAGCGCAAGAAGGCGGTGCT T A CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65855918..65856269 26863196 MeRIP-seq:(Medium) rs750964102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401081,Human_RBP_ID_1265416,Human_RBP_ID_1459372,Human_RBP_ID_1781560,Human_RBP_ID_2276411,Human_RBP_ID_4172834,Human_RBP_ID_8356154,Human_RBP_ID_9321589,Human_RBP_ID_9362519,Human_RBP_ID_17799376,Human_RBP_ID_18611150,Human_RBP_ID_22434627,Human_RBP_ID_22491630,Human_RBP_ID_22791860,Human_RBP_ID_23207001,Human_RBP_ID_23515580,Human_RBP_ID_27205325 Human_Splice_Rec_1260406,Human_Splice_Rec_1260414,Human_Splice_Rec_1260420,Human_Splice_Rec_1260422,Human_Splice_Rec_1260428,Human_Splice_Rec_1260438,Human_Splice_Rec_1260444,Human_Splice_Rec_1260452,Human_Splice_Rec_1260462,Human_Splice_Rec_1260466 Human_miRNA_ID_2016116 RMVar_hsa_circ_352,RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_94924,RMVar_hsa_circ_150780 56990 RMVar_ID_56990 Human_SNP_ID_470147194 m1A Human chr11 - 65856168 65856168 65856168 AACGACATGAAGGTGCGTAAGTCTTCAACGCCAGAGGAGGTGAAGAAGCGCAAGAAGGCGGTGCT AACGACATGAAGGTGCGTAAGTCTTCAACGCCCGAGGAGGTGAAGAAGCGCAAGAAGGCGGTGCT T G CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65855918..65856269 26863196 MeRIP-seq:(Medium) rs750964102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401081,Human_RBP_ID_1265416,Human_RBP_ID_1459372,Human_RBP_ID_1781560,Human_RBP_ID_2276411,Human_RBP_ID_4172834,Human_RBP_ID_8356154,Human_RBP_ID_9321589,Human_RBP_ID_9362519,Human_RBP_ID_17799376,Human_RBP_ID_18611150,Human_RBP_ID_22434627,Human_RBP_ID_22491630,Human_RBP_ID_22791860,Human_RBP_ID_23207001,Human_RBP_ID_23515580,Human_RBP_ID_27205325 Human_Splice_Rec_1260406,Human_Splice_Rec_1260414,Human_Splice_Rec_1260420,Human_Splice_Rec_1260422,Human_Splice_Rec_1260428,Human_Splice_Rec_1260438,Human_Splice_Rec_1260444,Human_Splice_Rec_1260452,Human_Splice_Rec_1260462,Human_Splice_Rec_1260466 Human_miRNA_ID_2016116 RMVar_hsa_circ_352,RMVar_hsa_circ_105288,RMVar_hsa_circ_150781,RMVar_hsa_circ_94924,RMVar_hsa_circ_150780 56991 RMVar_ID_56991 Human_SNP_ID_470148006 m1A Human chr11 - 65858082 65858082 65858082 TTCGTTTCCGGAAACATGGTGAGCGGCAGGCCACGGCGCCTGAGGGAGGCGGCTGCGGGTCGGTC TTCGTTTCCGGAAACATGGTGAGCGGCAGGCCGCGGCGCCTGAGGGAGGCGGCTGCGGGTCGGTC T C CFL1 Ensembl:ENSG00000172757 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65858076..65858314 26863410 MeRIP-seq:(Medium) rs1484497474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808467,Human_RBP_ID_21965423 RMVar_hsa_circ_94924,RMVar_hsa_circ_150780 56992 RMVar_ID_56992 Human_SNP_ID_470148060 m1A Human chr11 + 65858156 65858156 65858156 GCACCGAGAGCCGCAGAAGACGAGAGCGCTGCAGCCGCTGCCGGGACCCGACTGAACGCGGCCTC GCACCGAGAGCCGCAGAAGACGAGAGCGCTGCCGCCGCTGCCGGGACCCGACTGAACGCGGCCTC A C MUS81 Ensembl:ENSG00000172732 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:65858076..65858225 26863196 MeRIP-seq:(Medium) rs1050982509 Functional Loss SNV dbSNP153 33..33 33 - - - 56993 RMVar_ID_56993 Human_SNP_ID_470149908 m1A Human chr11 + 65863154 65863154 65863154 CCTGAGCTTGCTGAATGTGGGCATCGGGCCCAAGGAGCCCCCTGGGGAGGAGACAGCAGTGCCAG CCTGAGCTTGCTGAATGTGGGCATCGGGCCCAGGGAGCCCCCTGGGGAGGAGACAGCAGTGCCAG A G MUS81 Ensembl:ENSG00000172732 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65863104..65863230 26863196 MeRIP-seq:(Medium) rs765478661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940844,Human_RBP_ID_18974191,Human_RBP_ID_26318757,Human_RBP_ID_27804695 Human_Splice_Rec_1260572,Human_Splice_Rec_1260573,Human_Splice_Rec_1260602,Human_Splice_Rec_1260603,Human_Splice_Rec_1260630,Human_Splice_Rec_1260642,Human_Splice_Rec_1260643,Human_Splice_Rec_1260670,Human_Splice_Rec_1260671,Human_Splice_Rec_1260692,Human_Splice_Rec_1260693,Human_Splice_Rec_1260700,Human_Splice_Rec_1260701,Human_Splice_Rec_1260714,Human_Splice_Rec_1260715,Human_Splice_Rec_1260721 RMVar_hsa_circ_122860,RMVar_hsa_circ_73916,RMVar_hsa_circ_150787 56994 RMVar_ID_56994 Human_SNP_ID_470150092 m1A Human chr11 + 65863665 65863638 65863665 ACAGCGGCTGCACGTGACCCACACGGTGCGCAAGCTGCACGTTGGAGATTTTGTGTGGGTGGCCC ACAGCG___________________________GCTGCACGTTGGAGATTTTGTGTGGGTGGCCC GGCTGCACGTGACCCACACGGTGCGCAA G MUS81 Ensembl:ENSG00000172732 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65863426..65863810 26863196 MeRIP-seq:(Medium) rs751250230 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_8356162,Human_RBP_ID_22895167 Human_Splice_Rec_1260576,Human_Splice_Rec_1260577,Human_Splice_Rec_1260606,Human_Splice_Rec_1260607,Human_Splice_Rec_1260646,Human_Splice_Rec_1260647,Human_Splice_Rec_1260674,Human_Splice_Rec_1260675,Human_Splice_Rec_1260718,Human_Splice_Rec_1260724,Human_Splice_Rec_1260725 RMVar_hsa_circ_122860,RMVar_hsa_circ_5822,RMVar_hsa_circ_73916,RMVar_hsa_circ_150787 56995 RMVar_ID_56995 Human_SNP_ID_470150111 m1A Human chr11 + 65863665 65863665 65863665 ACAGCGGCTGCACGTGACCCACACGGTGCGCAAGCTGCACGTTGGAGATTTTGTGTGGGTGGCCC ACAGCGGCTGCACGTGACCCACACGGTGCGCAGGCTGCACGTTGGAGATTTTGTGTGGGTGGCCC A G MUS81 Ensembl:ENSG00000172732 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65863426..65863810 26863196 MeRIP-seq:(Medium) rs1320652215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8356162,Human_RBP_ID_22895167 Human_Splice_Rec_1260576,Human_Splice_Rec_1260577,Human_Splice_Rec_1260606,Human_Splice_Rec_1260607,Human_Splice_Rec_1260646,Human_Splice_Rec_1260647,Human_Splice_Rec_1260674,Human_Splice_Rec_1260675,Human_Splice_Rec_1260718,Human_Splice_Rec_1260724,Human_Splice_Rec_1260725 RMVar_hsa_circ_122860,RMVar_hsa_circ_5822,RMVar_hsa_circ_73916,RMVar_hsa_circ_150787 56996 RMVar_ID_56996 Human_SNP_ID_470150731 m1A Human chr11 - 65865325 65865325 65865325 GGCTGAGGACACCTAAGGGCCCTTTAGGGCCTACCTGGCAGGGGTGCTGTATCGATCCACCAGGG GGCTGAGGACACCTAAGGGCCCTTTAGGGCCTCCCTGGCAGGGGTGCTGTATCGATCCACCAGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65865201..65865341;chr11:65865226..65865377;chr11:65865226..65865325 26863196 MeRIP-seq:(Medium) rs1362018193 Functional Loss SNV dbSNP153 33..33 33 - - - 56997 RMVar_ID_56997 Human_SNP_ID_470153285 m1A Human chr11 - 65873218 65873218 65873218 AAAATTTTGCAGGGAGCAGATTGAGGGTCTGGAGGACTGGGTTAGGTGGGCTCTAGGTACCCAGG AAAATTTTGCAGGGAGCAGATTGAGGGTCTGGTGGACTGGGTTAGGTGGGCTCTAGGTACCCAGG T A EFEMP2 Ensembl:ENSG00000172638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65873011..65873325 26863196 MeRIP-seq:(Medium) rs893824318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940852 56998 RMVar_ID_56998 Human_SNP_ID_470153363 m1A Human chr11 + 65873510 65873507 65873510 CTTTTGGCACAAAATGAATGGAAGCCCCTGAGAAGGAGGGCAGGGCTGATGTCGGACGTGCGGGA CTTTTGGCACAAAATGAATGGAAGCCCCTG___AGGAGGGCAGGGCTGATGTCGGACGTGCGGGA GAGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65873508..65873584 26863196 MeRIP-seq:(Medium) rs569388347 Functional Loss DEL dbSNP153 31..33 33 - - - 56999 RMVar_ID_56999 Human_SNP_ID_470156727 m1A Human chr11 - 65885169 65885169 65885169 TTCATGGCCTCACAGACTCACAGATGGATGACATGGACATGGACTTAGACAAGGAATTTCTCCAG TTCATGGCCTCACAGACTCACAGATGGATGACGTGGACATGGACTTAGACAAGGAATTTCTCCAG T C FIBP Ensembl:ENSG00000172500 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65885118..65885218 26863196 MeRIP-seq:(Medium) rs1473887510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1459383,Human_RBP_ID_1781563,Human_RBP_ID_5165703,Human_RBP_ID_11675593 Human_Splice_Rec_1260978,Human_Splice_Rec_1260979,Human_Splice_Rec_1260988,Human_Splice_Rec_1260989,Human_Splice_Rec_1261004,Human_Splice_Rec_1261005,Human_Splice_Rec_1261022,Human_Splice_Rec_1261023,Human_Splice_Rec_1261040,Human_Splice_Rec_1261041,Human_Splice_Rec_1261056,Human_Splice_Rec_1261057,Human_Splice_Rec_1261066,Human_Splice_Rec_1261067,Human_Splice_Rec_1261076,Human_Splice_Rec_1261077 Human_miRNA_ID_1747314 RMVar_hsa_circ_24457,RMVar_hsa_circ_150807,RMVar_hsa_circ_13643,RMVar_hsa_circ_305782 57000 RMVar_ID_57000 Human_SNP_ID_470156886 m1A Human chr11 + 65885580 65885578 65885580 AGTTTTGGATCATGAGCTCAGCGCAGAAGGCAAAGTCACCGAAGCTCAGATACTGCAGTTTTTTC AGTTTTGGATCATGAGCTCAGCGCAGAAGGC__AGTCACCGAAGCTCAGATACTGCAGTTTTTTC CAA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65885444..65885650 32194978 MeRIP-seq:(Medium) rs1565281237 Functional Loss DEL dbSNP153 32..33 33 - - - 57001 RMVar_ID_57001 Human_SNP_ID_470156887 m1A Human chr11 + 65885580 65885580 65885580 AGTTTTGGATCATGAGCTCAGCGCAGAAGGCAAAGTCACCGAAGCTCAGATACTGCAGTTTTTTC AGTTTTGGATCATGAGCTCAGCGCAGAAGGCAGAGTCACCGAAGCTCAGATACTGCAGTTTTTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65885444..65885650 32194978 MeRIP-seq:(Medium) rs1210501506 Functional Loss SNV dbSNP153 33..33 33 - - - 57002 RMVar_ID_57002 Human_SNP_ID_470157736 m1A Human chr11 - 65888076 65888076 65888076 TGCGCTCGGGAATCCTGGAGCAGACTGGCGCCACGGCAGCGGTGCTGCAGAGCGACACCATGGAC TGCGCTCGGGAATCCTGGAGCAGACTGGCGCCGCGGCAGCGGTGCTGCAGAGCGACACCATGGAC T C FIBP Ensembl:ENSG00000172500 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65888026..65888150 26863196 MeRIP-seq:(Medium) rs1007774881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1260970,Human_Splice_Rec_1260996,Human_Splice_Rec_1261032,Human_Splice_Rec_1261050,Human_Splice_Rec_1261070,Human_Splice_Rec_1261080,Human_Splice_Rec_1261088,Human_Splice_Rec_1261096,Human_Splice_Rec_1261100 Human_miRNA_ID_2027319,Human_miRNA_ID_2395450 RMVar_hsa_circ_11580,RMVar_hsa_circ_372939,RMVar_hsa_circ_150808 57003 RMVar_ID_57003 Human_SNP_ID_470157737 m1A Human chr11 - 65888076 65888076 65888076 TGCGCTCGGGAATCCTGGAGCAGACTGGCGCCACGGCAGCGGTGCTGCAGAGCGACACCATGGAC TGCGCTCGGGAATCCTGGAGCAGACTGGCGCCCCGGCAGCGGTGCTGCAGAGCGACACCATGGAC T G FIBP Ensembl:ENSG00000172500 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65888026..65888150 26863196 MeRIP-seq:(Medium) rs1007774881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1260970,Human_Splice_Rec_1260996,Human_Splice_Rec_1261032,Human_Splice_Rec_1261050,Human_Splice_Rec_1261070,Human_Splice_Rec_1261080,Human_Splice_Rec_1261088,Human_Splice_Rec_1261096,Human_Splice_Rec_1261100 Human_miRNA_ID_2027319,Human_miRNA_ID_2395450 RMVar_hsa_circ_11580,RMVar_hsa_circ_372939,RMVar_hsa_circ_150808 57004 RMVar_ID_57004 Human_SNP_ID_470157744 m1A Human chr11 - 65888087 65888087 65888087 GGCCCTGCGGGTGCGCTCGGGAATCCTGGAGCAGACTGGCGCCACGGCAGCGGTGCTGCAGAGCG GGCCCTGCGGGTGCGCTCGGGAATCCTGGAGCGGACTGGCGCCACGGCAGCGGTGCTGCAGAGCG T C FIBP Ensembl:ENSG00000172500 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr11:65888036..65888198;chr11:65887943..65888342 26863196,32194978 MeRIP-seq:(Medium) rs1435227102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401115 Human_Splice_Rec_1260970,Human_Splice_Rec_1260996,Human_Splice_Rec_1261032,Human_Splice_Rec_1261050,Human_Splice_Rec_1261070,Human_Splice_Rec_1261080,Human_Splice_Rec_1261088,Human_Splice_Rec_1261096,Human_Splice_Rec_1261100 Human_miRNA_ID_2027319 RMVar_hsa_circ_11580,RMVar_hsa_circ_372939,RMVar_hsa_circ_150808 57005 RMVar_ID_57005 Human_SNP_ID_470158582 m1A Human chr11 + 65890848 65890848 65890848 GACGGACGAGGAGATGGCGGCGCTAGGCAAGGAAGAGCTAGTGCGGCGCCTGCGGCGGGAGGAGG GACGGACGAGGAGATGGCGGCGCTAGGCAAGGGAGAGCTAGTGCGGCGCCTGCGGCGGGAGGAGG A G CCDC85B Ensembl:ENSG00000175602 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65890626..65891586 26863196 MeRIP-seq:(Medium) rs1440084958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401118,Human_RBP_ID_5111321,Human_RBP_ID_8940562,Human_RBP_ID_17649730 57006 RMVar_ID_57006 Human_SNP_ID_470158585 m1A Human chr11 + 65890855 65890855 65890855 GAGGAGATGGCGGCGCTAGGCAAGGAAGAGCTAGTGCGGCGCCTGCGGCGGGAGGAGGCGGCGCG GAGGAGATGGCGGCGCTAGGCAAGGAAGAGCTGGTGCGGCGCCTGCGGCGGGAGGAGGCGGCGCG A G CCDC85B Ensembl:ENSG00000175602 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65890651..65890876 26863196 MeRIP-seq:(Medium) rs769098632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401118,Human_RBP_ID_5111321,Human_RBP_ID_8940562,Human_RBP_ID_17649730,Human_RBP_ID_22433765 57007 RMVar_ID_57007 Human_SNP_ID_470160341 m1A Human chr11 - 65897005 65897005 65897005 CATCTGTGGCCTTCCATTTCTTATTCCTTAGAAGTTCCACCTGGTGCCAAGCATCAACACCATGA CATCTGTGGCCTTCCATTTCTTATTCCTTAGAGGTTCCACCTGGTGCCAAGCATCAACACCATGA T C FOSL1 Ensembl:ENSG00000175592 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65896984..65897059 26863196 MeRIP-seq:(Medium) rs757312993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32642 Human_Splice_Rec_1261102,Human_Splice_Rec_1261110,Human_Splice_Rec_1261114 RMVar_hsa_circ_290135,RMVar_hsa_circ_336721 57008 RMVar_ID_57008 Human_SNP_ID_470165577 m1A Human chr11 + 65917513 65917513 65917513 GCACGGTCAAGCACTCGGGAGCCACGGGCACTACCCCCAAGCTGGAAACGGCTCTCATAGAGAGT GCACGGTCAAGCACTCGGGAGCCACGGGCACTGCCCCCAAGCTGGAAACGGCTCTCATAGAGAGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65916926..65918324 32194978 MeRIP-seq:(Medium) rs758141591 Functional Loss SNV dbSNP153 33..33 33 - - - 57009 RMVar_ID_57009 Human_SNP_ID_470165872 m1A Human chr11 - 65918217 65918217 65918217 CAGACCCTGCCCTGACTCGGTTCCCTCACAGCAGGATGGAACCAGGTGAGGAGCTGGAAGAGGAG CAGACCCTGCCCTGACTCGGTTCCCTCACAGCGGGATGGAACCAGGTGAGGAGCTGGAAGAGGAG T C C11orf68 Ensembl:ENSG00000175573 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65918074..65918275 26863196 MeRIP-seq:(Medium) rs1448924384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1261124 RMVar_hsa_circ_83668,RMVar_hsa_circ_150810 57010 RMVar_ID_57010 Human_SNP_ID_470166195 m1A Human chr11 + 65918997 65918997 65918997 GCCGTGGCTCCGCGCCACCGCCACCGCGCCCCACCCCCGCCACGGCCGCCGCCGCCGCCGCCGCC GCCGTGGCTCCGCGCCACCGCCACCGCGCCCCCCCCCCGCCACGGCCGCCGCCGCCGCCGCCGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65918809..65919075;chr11:65918807..65919050;chr11:65918849..65919068 26863196 MeRIP-seq:(Medium) rs999053322 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57011 RMVar_ID_57011 Human_SNP_ID_470166711 m1A Human chr11 - 65920043 65920043 65920043 ACCCGCCGGCCCCTCCCGGCTCCTCGCCGCTCACAGGTGGGATGTGGTCATGGTCTTCGCGTTCC ACCCGCCGGCCCCTCCCGGCTCCTCGCCGCTCTCAGGTGGGATGTGGTCATGGTCTTCGCGTTCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:65919926..65920170 32194978 MeRIP-seq:(Medium) rs113300200 Functional Loss SNV dbSNP153 33..33 33 - - - 57012 RMVar_ID_57012 Human_SNP_ID_470167182 m1A Human chr11 + 65921297 65921277 65921297 CAGCTGCCCCTGTGGAGGGCACGGTGGGGCTCAGGCCTGACTCTCTCCTGCCTTCTGCCCTGCAG CAGCTGCCCCTGT____________________GGCCTGACTCTCTCCTGCCTTCTGCCCTGCAG TGGAGGGCACGGTGGGGCTCA T DRAP1 Ensembl:ENSG00000175550 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65921294..65921507 26863196 MeRIP-seq:(Medium) rs1161721698 Functional Loss DEL dbSNP153 14..33 33 - - - 57013 RMVar_ID_57013 Human_SNP_ID_470178693 m1A Human chr11 + 65964055 65964055 65964055 GGCTTCTTGGCCCTGTGTTCAGCTCCTGAGCCATGCTTCTTCTTGTTCCAGCTGCCAGCTCCAAA GGCTTCTTGGCCCTGTGTTCAGCTCCTGAGCCGTGCTTCTTCTTGTTCCAGCTGCCAGCTCCAAA A G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65964051..65964150 26863196 MeRIP-seq:(Medium) rs772949210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1261244,Human_Splice_Rec_1261247,Human_Splice_Rec_1261262,Human_Splice_Rec_1261263,Human_Splice_Rec_1261269,Human_Splice_Rec_1261277 57014 RMVar_ID_57014 Human_SNP_ID_470179070 m1A Human chr11 + 65965210 65965210 65965210 GCGGCTGCCAAGGAGAAGCGCCTGCTGAACCAAAAGCTGGGGTGAGGGGTCCTGGCCAGGGCAGG GCGGCTGCCAAGGAGAAGCGCCTGCTGAACCAGAAGCTGGGGTGAGGGGTCCTGGCCAGGGCAGG A G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65965076..65965251 26863196 MeRIP-seq:(Medium) rs866857445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17804656,Human_RBP_ID_18974219 Human_Splice_Rec_1261251,Human_Splice_Rec_1261273,Human_Splice_Rec_1261281 Human_miRNA_ID_2359808 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184 57015 RMVar_ID_57015 Human_SNP_ID_470179269 m1A Human chr11 + 65965769 65965769 65965769 TGTCAGCACTCTGGTGGAGGAGGAGTTCGGGCAGAGGCGGCAGGTGAGGCTGCAGCAGGGGTGGT TGTCAGCACTCTGGTGGAGGAGGAGTTCGGGCCGAGGCGGCAGGTGAGGCTGCAGCAGGGGTGGT A C SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65965076..65966247 26863196 MeRIP-seq:(Medium) rs763406087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227153,Human_RBP_ID_871254,Human_RBP_ID_3940856,Human_RBP_ID_5110524,Human_RBP_ID_8773737,Human_RBP_ID_9362532,Human_RBP_ID_18972312,Human_RBP_ID_22034692,Human_RBP_ID_26317809 Human_Splice_Rec_1261254,Human_Splice_Rec_1261255,Human_Splice_Rec_1261284,Human_Splice_Rec_1261285 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184 57016 RMVar_ID_57016 Human_SNP_ID_470179433 m1A Human chr11 + 65966159 65966157 65966160 AGGAGCGGGCAGAGAAAAATGTGGAGCTGCGGAAGAAGAAGCCTGACTACCTGCCCTATGCCGAG AGGAGCGGGCAGAGAAAAATGTGGAGCTGCG___GAAGAAGCCTGACTACCTGCCCTATGCCGAG GGAA G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65964546..65966246 32194978 MeRIP-seq:(Medium) rs775356602 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3378239,Human_RBP_ID_4173072,Human_RBP_ID_5550051,Human_RBP_ID_8229263,Human_RBP_ID_8774366,Human_RBP_ID_9362534,Human_RBP_ID_18410507,Human_RBP_ID_18972315,Human_RBP_ID_26318785 Human_Splice_Rec_1261258,Human_Splice_Rec_1261288 Human_miRNA_ID_2169929 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184 57017 RMVar_ID_57017 Human_SNP_ID_470179600 m1A Human chr11 + 65966511 65966511 65966511 AAGCTGCGGCTGCAGGCTCAGTCCCTGAGCACAGTGGGGCCCCGGCTGGCCTCCGAATACCTCAC AAGCTGCGGCTGCAGGCTCAGTCCCTGAGCACGGTGGGGCCCCGGCTGGCCTCCGAATACCTCAC A G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65966330..65966581 26863196 MeRIP-seq:(Medium) rs1286589424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31621,Human_RBP_ID_8773741,Human_RBP_ID_9275904 Human_Splice_Rec_1261259,Human_Splice_Rec_1261289 Human_miRNA_ID_2295599,Human_miRNA_ID_2397745 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184,RMVar_hsa_circ_336615 57018 RMVar_ID_57018 Human_SNP_ID_470179954 m1A Human chr11 + 65967533 65967533 65967533 CGAAGTGGAGGAGGAGAAGGAGCCTGTGCCTCAGCCCCTGCCGTCGGACGACACCCGAGTGGAGA CGAAGTGGAGGAGGAGAAGGAGCCTGTGCCTCGGCCCCTGCCGTCGGACGACACCCGAGTGGAGA A G SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65967476..65967672 26863196 MeRIP-seq:(Medium) rs200869280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32628,Human_RBP_ID_8774371,Human_RBP_ID_9275907,Human_RBP_ID_9362537,Human_RBP_ID_18974225,Human_RBP_ID_22532297,Human_RBP_ID_27804723 Human_Splice_Rec_1261292,Human_Splice_Rec_1261293 RMVar_hsa_circ_11768,RMVar_hsa_circ_71217,RMVar_hsa_circ_265184,RMVar_hsa_circ_71859,RMVar_hsa_circ_68143 57019 RMVar_ID_57019 Human_SNP_ID_470181152 m1A Human chr11 + 65971637 65971608 65971637 AGCTGCTGAGGAGGGGGATGGTGGGATTCAGGAGCTGAGGAGGGGGATGGTGGGATTAATGCCCT AGCT_____________________________GCTGAGGAGGGGGATGGTGGGATTAATGCCCT TGCTGAGGAGGGGGATGGTGGGATTCAGGA T SART1 Ensembl:ENSG00000175467 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65971635..65971872 26863196 MeRIP-seq:(Medium) rs1432131214 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_3387985,Human_RBP_ID_8174423,Human_RBP_ID_9415039 RMVar_hsa_circ_71217 57020 RMVar_ID_57020 Human_SNP_ID_470182446 m1A Human chr11 - 65975809 65975809 65975809 CTCCTGTCGCAGATGCCCAGCCACACACAATGATTACCATCTCCCCTCTTTAAAAAACTTCTCCC CTCCTGTCGCAGATGCCCAGCCACACACAATGGTTACCATCTCCCCTCTTTAAAAAACTTCTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65975807..65975934 26863196 MeRIP-seq:(Medium) rs555188697 Functional Loss SNV dbSNP153 33..33 33 - - - 57021 RMVar_ID_57021 Human_SNP_ID_470183148 m1A Human chr11 + 65977888 65977886 65977888 TCGAATACGTGGATGAGACGGGCCGGAAACTCACACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG TCGAATACGTGGATGAGACGGGCCGGAAACT__CACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG TCA T SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65977745..65977936 26863196 MeRIP-seq:(Medium) rs1565318905 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8771092,Human_RBP_ID_9276554 Human_Splice_Rec_1261305,Human_Splice_Rec_1261317 RMVar_hsa_circ_34404,RMVar_hsa_circ_58674,RMVar_hsa_circ_377971,RMVar_hsa_circ_28275 57022 RMVar_ID_57022 Human_SNP_ID_470183150 m1A Human chr11 + 65977888 65977888 65977888 TCGAATACGTGGATGAGACGGGCCGGAAACTCACACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG TCGAATACGTGGATGAGACGGGCCGGAAACTCGCACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG A G SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65977745..65977936 26863196 MeRIP-seq:(Medium) rs1183056469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8771092,Human_RBP_ID_9276554 Human_Splice_Rec_1261305,Human_Splice_Rec_1261317 RMVar_hsa_circ_34404,RMVar_hsa_circ_58674,RMVar_hsa_circ_377971,RMVar_hsa_circ_28275 57023 RMVar_ID_57023 Human_SNP_ID_470183151 m1A Human chr11 + 65977888 65977888 65977888 TCGAATACGTGGATGAGACGGGCCGGAAACTCACACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG TCGAATACGTGGATGAGACGGGCCGGAAACTCTCACCCAAGGAGGTGAGCAGGGCCTTTTGCAGG A T SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65977745..65977936 26863196 MeRIP-seq:(Medium) rs1183056469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8771092,Human_RBP_ID_9276554 Human_Splice_Rec_1261305,Human_Splice_Rec_1261317 RMVar_hsa_circ_34404,RMVar_hsa_circ_58674,RMVar_hsa_circ_377971,RMVar_hsa_circ_28275 57024 RMVar_ID_57024 Human_SNP_ID_470183423 m1A Human chr11 + 65978679 65978679 65978679 GATGAAGACAGAGCGGCGGATGAAGAAGCTGGACGAGGAGGCGGTGGGTGCCCTTGGGGATGTGG GATGAAGACAGAGCGGCGGATGAAGAAGCTGGGCGAGGAGGCGGTGGGTGCCCTTGGGGATGTGG A G SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:65978570..65978925;chr11:65978569..65979036;chr11:65978558..65978925 26863196 MeRIP-seq:(Medium) rs1196042272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5110884,Human_RBP_ID_6086642,Human_RBP_ID_9275912,Human_RBP_ID_24542525 Human_Splice_Rec_1261306,Human_Splice_Rec_1261307,Human_Splice_Rec_1261318,Human_Splice_Rec_1261319,Human_Splice_Rec_1261321 RMVar_hsa_circ_377971,RMVar_hsa_circ_28275 57025 RMVar_ID_57025 Human_SNP_ID_470189726 m1A Human chr11 + 66002090 66002090 66002090 CGTCAGTTAGAAATCAGGTCTCCAGTGTTCCCAGTTCCCACCAGTCCAACTGCGAGGAGTGCGAC CGTCAGTTAGAAATCAGGTCTCCAGTGTTCCCGGTTCCCACCAGTCCAACTGCGAGGAGTGCGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66001967..66002136;chr11:66001978..66002111 26863196 MeRIP-seq:(Medium) rs886048511 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_159 RMVar_hsa_circ_82570,RMVar_hsa_circ_150814 57026 RMVar_ID_57026 Human_SNP_ID_470189727 m1A Human chr11 + 66002090 66002090 66002090 CGTCAGTTAGAAATCAGGTCTCCAGTGTTCCCAGTTCCCACCAGTCCAACTGCGAGGAGTGCGAC CGTCAGTTAGAAATCAGGTCTCCAGTGTTCCCTGTTCCCACCAGTCCAACTGCGAGGAGTGCGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66001967..66002136;chr11:66001978..66002111 26863196 MeRIP-seq:(Medium) rs886048511 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_159 RMVar_hsa_circ_82570,RMVar_hsa_circ_150814 57027 RMVar_ID_57027 Human_SNP_ID_470189878 m1A Human chr11 + 66002525 66002525 66002525 AGAAAGTTCTAGTGGCTTGAGGTATCCGCAGGAGCGGCCGGGTGGCGGGAGGAACCGTTACGGGA AGAAAGTTCTAGTGGCTTGAGGTATCCGCAGGGGCGGCCGGGTGGCGGGAGGAACCGTTACGGGA A G BANF1 Ensembl:ENSG00000175334 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66002476..66002869 26863196 MeRIP-seq:(Medium) rs886048516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227148,Human_RBP_ID_401174,Human_RBP_ID_988049,Human_RBP_ID_4185128,Human_RBP_ID_5110886,Human_RBP_ID_5138677,Human_RBP_ID_5313712,Human_RBP_ID_5416225,Human_RBP_ID_5461173,Human_RBP_ID_5490126,Human_RBP_ID_9322217,Human_RBP_ID_18416599,Human_RBP_ID_19049933,Human_RBP_ID_22433120,Human_RBP_ID_23207003 Human_Splice_Rec_1261415,Human_Splice_Rec_1261417 Human_miRNA_ID_3115116 Clinvar_Rec_160 RMVar_hsa_circ_82570,RMVar_hsa_circ_150814 57028 RMVar_ID_57028 Human_SNP_ID_470190304 m1A Human chr11 - 66003583 66003580 66003583 GGGAAAAGGAAGGAGCGTGCTGCTCAGTGCTCAGTGAGAGATAAGAGCAAGACAGCCATTCCTGT GGGAAAAGGAAGGAGCGTGCTGCTCAGTGCTC___GAGAGATAAGAGCAAGACAGCCATTCCTGT CACT C lnc-EIF1AD-1 RNACentral:URS0000D5BCE1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66003580..66003774 26863196 MeRIP-seq:(Medium) rs775972466 Functional Loss DEL dbSNP153 33..35 33 - - - 57029 RMVar_ID_57029 Human_SNP_ID_470193974 m1A Human chr11 + 66017091 66017091 66017091 CCTCAAATGTGGTGTCCACAATCTCATCGATGACGGCTGCCTGGGAGCGGAACTTCTGCTGCTCC CCTCAAATGTGGTGTCCACAATCTCATCGATGGCGGCTGCCTGGGAGCGGAACTTCTGCTGCTCC A G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66016900..66018806 32194978 MeRIP-seq:(Medium) rs200011892 Functional Loss SNV dbSNP153 33..33 33 - - - 57030 RMVar_ID_57030 Human_SNP_ID_470193997 m1A Human chr11 - 66017135 66017135 66017135 GAGCTCCTGTTCCATTACCTGCAGCTGGTGGCAAGCGTGGAGCAGGAGCAGCAGAAGTTCCGCTC GAGCTCCTGTTCCATTACCTGCAGCTGGTGGCCAGCGTGGAGCAGGAGCAGCAGAAGTTCCGCTC T G CATSPER1 Ensembl:ENSG00000175294 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:66017093..66018856 32194978 MeRIP-seq:(Medium) rs750051513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1261454,Human_Splice_Rec_1261455,Human_Splice_Rec_1261464,Human_Splice_Rec_1261465 57031 RMVar_ID_57031 Human_SNP_ID_470194904 m1A Human chr11 + 66020348 66020347 66020348 CCTCCTGCTTCGCTTTCTCAAGGCCTTTGAACAGCGCCGTCTGGAAGCTATCCACCAGGACAGTA CCTCCTGCTTCGCTTTCTCAAGGCCTTTGAAC_GCGCCGTCTGGAAGCTATCCACCAGGACAGTA CA C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66020142..66020865 32194978 MeRIP-seq:(Medium) rs750657024 Functional Loss DEL dbSNP153 33..33 33 - - - 57032 RMVar_ID_57032 Human_SNP_ID_470196868 m1A Human chr11 - 66026128 66026128 66026128 CATGTCCACCAATCTCACCACCACAGCGAGGCACGGAATCACGGCAGAGCCCATGGCCCCACAGG CATGTCCACCAATCTCACCACCACAGCGAGGCGCGGAATCACGGCAGAGCCCATGGCCCCACAGG T C CATSPER1 Ensembl:ENSG00000175294 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66026124..66026231 26863196 MeRIP-seq:(Medium) rs199855584 Functional Loss SNV dbSNP153 33..33 33 - - - 57033 RMVar_ID_57033 Human_SNP_ID_470196885 m1A Human chr11 - 66026159 66026159 66026159 CCAAGACTTCCACGACCAAGCCTTGTCCTCCCATGTCCACCAATCTCACCACCACAGCGAGGCAC CCAAGACTTCCACGACCAAGCCTTGTCCTCCCGTGTCCACCAATCTCACCACCACAGCGAGGCAC T C CATSPER1 Ensembl:ENSG00000175294 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66026142..66026284 26863196 MeRIP-seq:(Medium) rs1414091764 Functional Loss SNV dbSNP153 33..33 33 - - - 57034 RMVar_ID_57034 Human_SNP_ID_470203821 m1A Human chr11 + 66052425 66052425 66052425 GGAGCATCCCGAGCCTCCCAAAGCAGAATTGCAGCTGCCGCCGCCGCCACCTCCAGGCCACTATG GGAGCATCCCGAGCCTCCCAAAGCAGAATTGCCGCTGCCGCCGCCGCCACCTCCAGGCCACTATG A C SF3B2 Ensembl:ENSG00000087365 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:66052376..66052540;chr11:66052376..66052450 26863196 MeRIP-seq:(Medium) rs536594368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227527,Human_RBP_ID_751983,Human_RBP_ID_807239,Human_RBP_ID_4185130,Human_RBP_ID_8774378,Human_RBP_ID_9254694,Human_RBP_ID_9275914,Human_RBP_ID_9362543,Human_RBP_ID_17682442,Human_RBP_ID_17799441,Human_RBP_ID_18611212,Human_RBP_ID_22433768,Human_RBP_ID_26317811 Human_Splice_Rec_1261483,Human_Splice_Rec_1261523,Human_Splice_Rec_1261565,Human_Splice_Rec_1261579,Human_Splice_Rec_1261597,Human_Splice_Rec_1261599,Human_Splice_Rec_1261605 57035 RMVar_ID_57035 Human_SNP_ID_470203859 m1A Human chr11 - 66052507 66052507 66052507 CTCGACTTCCTGTGTTCCTCACCCTGGATCGGAGCTCCGATCTCTGCCAACTTGGCCTGAAGCTC CTCGACTTCCTGTGTTCCTCACCCTGGATCGGGGCTCCGATCTCTGCCAACTTGGCCTGAAGCTC T C lnc-GAL3ST3-1 RNACentral:URS00008B91FC lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66052376..66052512 26863196 MeRIP-seq:(Medium) rs889054020 Functional Loss SNV dbSNP153 33..33 33 - - - 57036 RMVar_ID_57036 Human_SNP_ID_470203907 m1A Human chr11 - 66052628 66052628 66052628 GTACACGATCAATGGGGCAGGCCAGCCCGGCCAGGTCAGGCCCCAGCGGCCTGCCTCCGCCCCTC GTACACGATCAATGGGGCAGGCCAGCCCGGCCGGGTCAGGCCCCAGCGGCCTGCCTCCGCCCCTC T C lnc-GAL3ST3-1 RNACentral:URS00008B91FC lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66052624..66052764 26863196 MeRIP-seq:(Medium) rs752910709 Functional Loss SNV dbSNP153 33..33 33 - - - 57037 RMVar_ID_57037 Human_SNP_ID_470205069 m1A Human chr11 - 66056801 66056800 66056801 GGGAGGGAAGTGGGAGTAGATACTGCCTGAAAACGCATTTGGCAGGCAGCCCCTGGCAAATGCAT GGGAGGGAAGTGGGAGTAGATACTGCCTGAAA_CGCATTTGGCAGGCAGCCCCTGGCAAATGCAT GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66056797..66056981 26863196 MeRIP-seq:(Medium) rs1565087671 Functional Loss DEL dbSNP153 33..33 33 - - - 57038 RMVar_ID_57038 Human_SNP_ID_470205483 m1A Human chr11 - 66058143 66058143 66058143 CAGCATCAGAACGCCTGGCACTCACCCTGCTGAGAATTCATCTCTTCCTGGCGGCTCTCCTTCAG CAGCATCAGAACGCCTGGCACTCACCCTGCTGGGAATTCATCTCTTCCTGGCGGCTCTCCTTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66058023..66058187 26863196 MeRIP-seq:(Medium) rs1220476066 Functional Loss SNV dbSNP153 33..33 33 - - - 57039 RMVar_ID_57039 Human_SNP_ID_470205514 m1A Human chr11 + 66058268 66058268 66058268 CTTGGTAAAGGCAGGTTACTGTGAACGAGTGCAGGGCAGTGGCACCGTGAAGACTCATCACCACC CTTGGTAAAGGCAGGTTACTGTGAACGAGTGCCGGGCAGTGGCACCGTGAAGACTCATCACCACC A C SF3B2 Ensembl:ENSG00000087365 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66058266..66058432 26863196 MeRIP-seq:(Medium) rs1381235115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11676258 RMVar_hsa_circ_74717,RMVar_hsa_circ_14810,RMVar_hsa_circ_339833,RMVar_hsa_circ_14280,RMVar_hsa_circ_150818,RMVar_hsa_circ_150819,RMVar_hsa_circ_93752 57040 RMVar_ID_57040 Human_SNP_ID_470205678 m1A Human chr11 + 66058832 66058832 66058832 TGACCCAGCTGGTTTTCCTCCTCTTGACAGAAAAACCGGAAGCGTAGGAACCGAAAGAAGAAGAA TGACCCAGCTGGTTTTCCTCCTCTTGACAGAAGAACCGGAAGCGTAGGAACCGAAAGAAGAAGAA A G SF3B2 Ensembl:ENSG00000087365 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66058826..66058850 26863196 MeRIP-seq:(Medium) rs1221181153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29632,Human_RBP_ID_871654,Human_RBP_ID_2276517,Human_RBP_ID_5342727,Human_RBP_ID_9362552,Human_RBP_ID_22537622,Human_RBP_ID_22569556,Human_RBP_ID_22641656,Human_RBP_ID_23113131,Human_RBP_ID_24542529,Human_RBP_ID_26318805,Human_RBP_ID_26775656,Human_RBP_ID_27803668 Human_Splice_Rec_1261498,Human_Splice_Rec_1261540,Human_Splice_Rec_1261596,Human_Splice_Rec_1261622 RMVar_hsa_circ_53978,RMVar_hsa_circ_74717,RMVar_hsa_circ_14810,RMVar_hsa_circ_339833,RMVar_hsa_circ_150818,RMVar_hsa_circ_150819,RMVar_hsa_circ_93752,RMVar_hsa_circ_269693 57041 RMVar_ID_57041 Human_SNP_ID_470205813 m1A Human chr11 - 66059266 66059266 66059266 TCCTCTTCAAATCCCTTCTTCTTGGGGGCTGCAGAGTTCTCCAGTTTGTCAAGTTTCTCTGGCTC TCCTCTTCAAATCCCTTCTTCTTGGGGGCTGCGGAGTTCTCCAGTTTGTCAAGTTTCTCTGGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66059216..66059371 26863196 MeRIP-seq:(Medium) rs1380159340 Functional Loss SNV dbSNP153 33..33 33 - - - 57042 RMVar_ID_57042 Human_SNP_ID_470205870 m1A Human chr11 + 66059480 66059480 66059480 TGGGGTGGGTTGGGCAGTTTCATTCACATCTGAGTCCTGCTTAAAAGGGCTGATTGTTCTGTTCT TGGGGTGGGTTGGGCAGTTTCATTCACATCTGCGTCCTGCTTAAAAGGGCTGATTGTTCTGTTCT A C SF3B2 Ensembl:ENSG00000087365 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66059478..66059604 26863196 MeRIP-seq:(Medium) rs1342289233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22571297 RMVar_hsa_circ_74717,RMVar_hsa_circ_14810,RMVar_hsa_circ_339833,RMVar_hsa_circ_150818,RMVar_hsa_circ_150819,RMVar_hsa_circ_93752,RMVar_hsa_circ_269693,RMVar_hsa_circ_8917,RMVar_hsa_circ_67518 57043 RMVar_ID_57043 Human_SNP_ID_470205874 m1A Human chr11 - 66059504 66059500 66059504 TGGGGGCTTCTGGCTTCTTTTCCTAGAACAGAACAATCAGCCCTTTTAAGCAGGACTCAGATGTG TGGGGGCTTCTGGCTTCTTTTCCTAGAACAGA____TCAGCCCTTTTAAGCAGGACTCAGATGTG ATTGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:66059501..66059550 26863196 MeRIP-seq:(Medium) rs765928234 Functional Loss DEL dbSNP153 33..36 33 - - - 57044 RMVar_ID_57044 Human_SNP_ID_470206418 m1A Human chr11 - 66061695 66061695 66061695 TCCTGGCTTCTTCTCCTTCAGTCGTGTCTCGAACTCCTTCCCCTGAGGGAAAAGCAGAGCATGCT TCCTGGCTTCTTCTCCTTCAGTCGTGTCTCGAGCTCCTTCCCCTGAGGGAAAAGCAGAGCATGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66061676..66061725 26863196 MeRIP-seq:(Medium) rs755211760 Functional Loss SNV dbSNP153 33..33 33 - - - 57045 RMVar_ID_57045 Human_SNP_ID_470208008 m1A Human chr11 + 66068290 66068290 66068290 TGTGCGGGAGCAGCAGGCTCAAGTAGAGAAGGAGGACTTCAGTGACATGGTGGCTGAGCACGCTG TGTGCGGGAGCAGCAGGCTCAAGTAGAGAAGGGGGACTTCAGTGACATGGTGGCTGAGCACGCTG A G SF3B2 Ensembl:ENSG00000087365 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66067926..66068359 32194978 MeRIP-seq:(Medium) rs1310585922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29643,Human_RBP_ID_401236,Human_RBP_ID_749068,Human_RBP_ID_1459459,Human_RBP_ID_1781612,Human_RBP_ID_4173341,Human_RBP_ID_5110529,Human_RBP_ID_6086803,Human_RBP_ID_8229400,Human_RBP_ID_8771166,Human_RBP_ID_9275952,Human_RBP_ID_9362596,Human_RBP_ID_11676467,Human_RBP_ID_17799475,Human_RBP_ID_18159862,Human_RBP_ID_18410639,Human_RBP_ID_18611246,Human_RBP_ID_22034695,Human_RBP_ID_24363127,Human_RBP_ID_26318846,Human_RBP_ID_27803699 Human_Splice_Rec_1261521,Human_Splice_Rec_1261563,Human_Splice_Rec_1261659 RMVar_hsa_circ_150819,RMVar_hsa_circ_93752,RMVar_hsa_circ_267776,RMVar_hsa_circ_89582,RMVar_hsa_circ_64856,RMVar_hsa_circ_150826,RMVar_hsa_circ_280754,RMVar_hsa_circ_150827 57046 RMVar_ID_57046 Human_SNP_ID_470208166 m1A Human chr11 - 66068725 66068725 66068725 GTGTGAGGGGACCTAAAACTTGAACTCCTTATATTTCTTGCTGCCCCCACGGCTGTCCTGGGGCT GTGTGAGGGGACCTAAAACTTGAACTCCTTATGTTTCTTGCTGCCCCCACGGCTGTCCTGGGGCT T C AP006287.2 Ensembl:ENSG00000255038 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66068645..66068766 26863196 MeRIP-seq:(Medium) rs1428263891 Functional Loss SNV dbSNP153 33..33 33 - - - 57047 RMVar_ID_57047 Human_SNP_ID_470212183 m1A Human chr11 - 66084194 66084194 66084194 ATGTGTGTTCCATGTGGCCGGCTCGCTTTCTGAGGTCTTTCTAGACCACCTTGTTTAAAACCGTG ATGTGTGTTCCATGTGGCCGGCTCGCTTTCTGTGGTCTTTCTAGACCACCTTGTTTAAAACCGTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66084023..66084298 26863196 MeRIP-seq:(Medium) rs1352420509 Functional Loss SNV dbSNP153 33..33 33 - - - 57048 RMVar_ID_57048 Human_SNP_ID_470243198 m1A Human chr11 + 66219178 66219177 66219179 AGATGTCAGCTGAAGGCTGTTGCTATGATCCCAGAGAGGCAAGGAGAAAGGCCTGACTGGAAACA AGATGTCAGCTGAAGGCTGTTGCTATGATCCC__AGAGGCAAGGAGAAAGGCCTGACTGGAAACA CAG C PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66219174..66219318 26863196 MeRIP-seq:(Medium) rs1344787838 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_35747,RMVar_hsa_circ_101287,RMVar_hsa_circ_150828,RMVar_hsa_circ_83761,RMVar_hsa_circ_77681,RMVar_hsa_circ_95449,RMVar_hsa_circ_121403,RMVar_hsa_circ_150831,RMVar_hsa_circ_150832,RMVar_hsa_circ_349192,RMVar_hsa_circ_150836,RMVar_hsa_circ_120117,RMVar_hsa_circ_150835,RMVar_hsa_circ_89695,RMVar_hsa_circ_150839,RMVar_hsa_circ_150840 57049 RMVar_ID_57049 Human_SNP_ID_470243229 m1A Human chr11 - 66219314 66219306 66219314 CCTTGCACCCCGATCCTCTTACTGATGTCGCCAACACACCTGAACCAACATCTACGCCTGGAGTC CCTTGCACCCCGATCCTCTTACTGATGTCGCC________TGAACCAACATCTACGCCTGGAGTC AGGTGTGTT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66219114..66219517 26863196 MeRIP-seq:(Medium) rs991101804 Functional Loss DEL dbSNP153 33..40 33 - - - 57050 RMVar_ID_57050 Human_SNP_ID_470243229 m1A Human chr11 - 66219313 66219306 66219314 CTTGCACCCCGATCCTCTTACTGATGTCGCCAACACACCTGAACCAACATCTACGCCTGGAGTCT CTTGCACCCCGATCCTCTTACTGATGTCGCC________TGAACCAACATCTACGCCTGGAGTCT AGGTGTGTT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66219140..66219486 26863196 MeRIP-seq:(Medium) rs991101804 Functional Loss DEL dbSNP153 32..39 33 - - - 57051 RMVar_ID_57051 Human_SNP_ID_470246398 m1A Human chr11 - 66232185 66232185 66232185 ACACCAGGATCTGATTGAGCTGGTCATACACCACCTTTCTTGGAATCTGCAGGAACAAAAGAAAG ACACCAGGATCTGATTGAGCTGGTCATACACCGCCTTTCTTGGAATCTGCAGGAACAAAAGAAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66232176..66232250 32194978 MeRIP-seq:(Medium) rs747152812 Functional Loss SNV dbSNP153 33..33 33 - - - 57052 RMVar_ID_57052 Human_SNP_ID_470252567 m1A Human chr11 + 66257825 66257804 66257825 CGGGACCGGCTCGCGGGTGCGGGTCCGGGTGAAGCGGGAGGCAGCCAGAGTCGGAGCCGGGCCCG CGGGACCGGCTC_____________________GCGGGAGGCAGCCAGAGTCGGAGCCGGGCCCG CGCGGGTGCGGGTCCGGGTGAA C KLC2 Ensembl:ENSG00000174996 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:66257776..66257926 26863196 MeRIP-seq:(Medium) rs1188926941 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_227979,Human_RBP_ID_751652,Human_RBP_ID_866711,Human_RBP_ID_3384365,Human_RBP_ID_5138678,Human_RBP_ID_9414215,Human_RBP_ID_18416600,Human_RBP_ID_18974246,Human_RBP_ID_21883592 Human_Splice_Rec_1261855,Human_Splice_Rec_1261885,Human_Splice_Rec_1261913,Human_Splice_Rec_1261943,Human_Splice_Rec_1261953 57053 RMVar_ID_57053 Human_SNP_ID_470252571 m1A Human chr11 - 66257816 66257816 66257816 CTCCGACTCTGGCTGCCTCCCGCTTCACCCGGACCCGCACCCGCGAGCCGGTCCCGCCGCCTCCA CTCCGACTCTGGCTGCCTCCCGCTTCACCCGGCCCCGCACCCGCGAGCCGGTCCCGCCGCCTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:66257699..66258149;chr11:66257706..66258137;chr11:66257691..66258151 26863196 MeRIP-seq:(Medium) rs1050964196 Functional Loss SNV dbSNP153 33..33 33 - - - 57054 RMVar_ID_57054 Human_SNP_ID_470252573 m1A Human chr11 + 66257825 66257825 66257825 CGGGACCGGCTCGCGGGTGCGGGTCCGGGTGAAGCGGGAGGCAGCCAGAGTCGGAGCCGGGCCCG CGGGACCGGCTCGCGGGTGCGGGTCCGGGTGAGGCGGGAGGCAGCCAGAGTCGGAGCCGGGCCCG A G KLC2 Ensembl:ENSG00000174996 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:66257776..66257926 26863196 MeRIP-seq:(Medium) rs899074767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227979,Human_RBP_ID_751652,Human_RBP_ID_866711,Human_RBP_ID_3384365,Human_RBP_ID_5138678,Human_RBP_ID_9414215,Human_RBP_ID_18416600,Human_RBP_ID_18974246,Human_RBP_ID_21883592 Human_Splice_Rec_1261855,Human_Splice_Rec_1261885,Human_Splice_Rec_1261913,Human_Splice_Rec_1261943,Human_Splice_Rec_1261953 57055 RMVar_ID_57055 Human_SNP_ID_470252592 m1A Human chr11 - 66257873 66257873 66257873 ACCCCGTCTCCCGGCCCAATCGGCCCGCGCCGACCTGCGCCTGGTGCTCGGGCCCGGCTCCGACT ACCCCGTCTCCCGGCCCAATCGGCCCGCGCCGTCCTGCGCCTGGTGCTCGGGCCCGGCTCCGACT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:66257776..66257916 26863410 MeRIP-seq:(Medium) rs772440530 Functional Loss SNV dbSNP153 33..33 33 - - - 57056 RMVar_ID_57056 Human_SNP_ID_470253660 m1A Human chr11 + 66261875 66261875 66261875 TGAGGAGCTGGCGGGGACACAGCAGAAGCTGCAGCGCAGTGAGCAGGCCGTGGCCCAGCTCGAGG TGAGGAGCTGGCGGGGACACAGCAGAAGCTGCGGCGCAGTGAGCAGGCCGTGGCCCAGCTCGAGG A G KLC2 Ensembl:ENSG00000174996 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66261711..66262170 26863196 MeRIP-seq:(Medium) rs1215396703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227981,Human_RBP_ID_22895722 Human_Splice_Rec_1261819,Human_Splice_Rec_1261853,Human_Splice_Rec_1261859,Human_Splice_Rec_1261917,Human_Splice_Rec_1261947,Human_Splice_Rec_1261963,Human_Splice_Rec_1261991,Human_Splice_Rec_1262015,Human_Splice_Rec_1262017 RMVar_hsa_circ_362982 57057 RMVar_ID_57057 Human_SNP_ID_470254357 m1A Human chr11 - 66264123 66264123 66264123 AGTGCCCGCCGATAGTAATATTCCACCTCCTCAGCTTTGCCCTGGTTCTGGCACAGCAGGGCCAG AGTGCCCGCCGATAGTAATATTCCACCTCCTCTGCTTTGCCCTGGTTCTGGCACAGCAGGGCCAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66262825..66267661 32194978 MeRIP-seq:(Medium) rs1473698725 Functional Loss SNV dbSNP153 33..33 33 - - - 57058 RMVar_ID_57058 Human_SNP_ID_470254371 m1A Human chr11 - 66264165 66264165 66264165 ACATTGGGGTCATCGGGCCCGAGGCGTGTAGCATAGATCTCCAGTGCCCGCCGATAGTAATATTC ACATTGGGGTCATCGGGCCCGAGGCGTGTAGCGTAGATCTCCAGTGCCCGCCGATAGTAATATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66264101..66264234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 57059 RMVar_ID_57059 Human_SNP_ID_470254372 m1A Human chr11 - 66264168 66264168 66264168 GCCACATTGGGGTCATCGGGCCCGAGGCGTGTAGCATAGATCTCCAGTGCCCGCCGATAGTAATA GCCACATTGGGGTCATCGGGCCCGAGGCGTGTGGCATAGATCTCCAGTGCCCGCCGATAGTAATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66264117..66265682 26863196 MeRIP-seq:(Medium) rs1413227626 Functional Loss SNV dbSNP153 33..33 33 - - - 57060 RMVar_ID_57060 Human_SNP_ID_470257177 m1A Human chr11 + 66272353 66272353 66272353 CTCTGGACCTCAGCTGACCTGCTCCTCTGCCTACTGTCTCCTAGTGGGACACAGCGGGCCAGGAA CTCTGGACCTCAGCTGACCTGCTCCTCTGCCTCCTGTCTCCTAGTGGGACACAGCGGGCCAGGAA A C RAB1B Ensembl:ENSG00000174903 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66272351..66272475 26863196 MeRIP-seq:(Medium) rs375792546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20936,RMVar_hsa_circ_114115,RMVar_hsa_circ_341467,RMVar_hsa_circ_150860,RMVar_hsa_circ_321871,RMVar_hsa_circ_369499,RMVar_hsa_circ_150861 57061 RMVar_ID_57061 Human_SNP_ID_470257178 m1A Human chr11 + 66272353 66272353 66272353 CTCTGGACCTCAGCTGACCTGCTCCTCTGCCTACTGTCTCCTAGTGGGACACAGCGGGCCAGGAA CTCTGGACCTCAGCTGACCTGCTCCTCTGCCTGCTGTCTCCTAGTGGGACACAGCGGGCCAGGAA A G RAB1B Ensembl:ENSG00000174903 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66272351..66272475 26863196 MeRIP-seq:(Medium) rs375792546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20936,RMVar_hsa_circ_114115,RMVar_hsa_circ_341467,RMVar_hsa_circ_150860,RMVar_hsa_circ_321871,RMVar_hsa_circ_369499,RMVar_hsa_circ_150861 57062 RMVar_ID_57062 Human_SNP_ID_470257193 m1A Human chr11 + 66272414 66272414 66272414 GGAACGGTTCCGGACCATCACTTCCAGCTACTACCGGGGGGCTCATGGCATCATCGTGGTGTATG GGAACGGTTCCGGACCATCACTTCCAGCTACTTCCGGGGGGCTCATGGCATCATCGTGGTGTATG A T RAB1B Ensembl:ENSG00000174903 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66272338..66272492 26863196 MeRIP-seq:(Medium) rs1170642501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809133,Human_RBP_ID_988076,Human_RBP_ID_4173509,Human_RBP_ID_17350251,Human_RBP_ID_18972329,Human_RBP_ID_22791909,Human_RBP_ID_26803815,Human_RBP_ID_26895161 Human_Splice_Rec_1262044,Human_Splice_Rec_1262045 RMVar_hsa_circ_20936,RMVar_hsa_circ_114115,RMVar_hsa_circ_341467,RMVar_hsa_circ_150860,RMVar_hsa_circ_321871,RMVar_hsa_circ_369499,RMVar_hsa_circ_150861 57063 RMVar_ID_57063 Human_SNP_ID_470258374 m1A Human chr11 + 66276499 66276499 66276499 CTGCTGTGCTGTTGCCTCTAGGTGACTTTCCAAGATGCCCCCCTACACACCTTTCTTTGGAACGA CTGCTGTGCTGTTGCCTCTAGGTGACTTTCCAGGATGCCCCCCTACACACCTTTCTTTGGAACGA A G RAB1B Ensembl:ENSG00000174903 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66276448..66276580 26863196 MeRIP-seq:(Medium) rs1362745778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401299,Human_RBP_ID_988080,Human_RBP_ID_1163103,Human_RBP_ID_3378353,Human_RBP_ID_6087072,Human_RBP_ID_17465860,Human_RBP_ID_17799551,Human_RBP_ID_22791911,Human_RBP_ID_23515987,Human_RBP_ID_24461969,Human_RBP_ID_27557123 Human_miRNA_ID_1269380 RMVar_hsa_circ_114115,RMVar_hsa_circ_150860 57064 RMVar_ID_57064 Human_SNP_ID_470258556 m1A Human chr11 - 66277077 66277077 66277077 CTTCCCTGGTGGGCTCCAGAGACGGAGTGGGGAGTGAGCCAGATGTGCTACCTTGGGGAAAGGGA CTTCCCTGGTGGGCTCCAGAGACGGAGTGGGGGGTGAGCCAGATGTGCTACCTTGGGGAAAGGGA T C AP001107.2,AP001107.1 Ensembl:ENSG00000254452,Ensembl:ENSG00000245156 lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:66276973..66277127 26863196 MeRIP-seq:(Medium) rs1289742168 Functional Loss SNV dbSNP153 33..33 33 - - - 57065 RMVar_ID_57065 Human_SNP_ID_470259059 m1A Human chr11 + 66278380 66278354 66278381 CGAGCCCCACGGGCCATGCCCGGCCGGCCCTAAGCGCGGGCCGGGGGGCGTCCCCTTGCGCCCGG CGAGCCC___________________________CGCGGGCCGGGGGGCGTCCCCTTGCGCCCGG CCACGGGCCATGCCCGGCCGGCCCTAAG C CNIH2 Ensembl:ENSG00000174871 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:66278287..66278387 26863410 MeRIP-seq:(Medium) rs1382585078 Functional Loss DEL dbSNP153 8..34 33 - - - 57066 RMVar_ID_57066 Human_SNP_ID_470261017 m1A Human chr11 + 66284684 66284684 66284684 GAAAGTCAGCCAGTATATGATGAGGGGCTGGAAGGCTGCAGCTCCCAGAGTCAGGTAGAGCTGGA GAAAGTCAGCCAGTATATGATGAGGGGCTGGAGGGCTGCAGCTCCCAGAGTCAGGTAGAGCTGGA A G CNIH2 Ensembl:ENSG00000174871 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:66284626..66284882 26863196 MeRIP-seq:(Medium) rs1219077230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11679279 57067 RMVar_ID_57067 Human_SNP_ID_470261019 m1A Human chr11 + 66284691 66284691 66284691 AGCCAGTATATGATGAGGGGCTGGAAGGCTGCAGCTCCCAGAGTCAGGTAGAGCTGGAGACGCTG AGCCAGTATATGATGAGGGGCTGGAAGGCTGCCGCTCCCAGAGTCAGGTAGAGCTGGAGACGCTG A C CNIH2 Ensembl:ENSG00000174871 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:66284651..66284854 26863196 MeRIP-seq:(Medium) rs1439284436 Functional Loss SNV dbSNP153 33..33 33 - - - 57068 RMVar_ID_57068 Human_SNP_ID_470261028 m1A Human chr11 + 66284710 66284710 66284710 GCTGGAAGGCTGCAGCTCCCAGAGTCAGGTAGAGCTGGAGACGCTGCCGGGGGACGGGGCCCCCC GCTGGAAGGCTGCAGCTCCCAGAGTCAGGTAGTGCTGGAGACGCTGCCGGGGGACGGGGCCCCCC A T CNIH2 Ensembl:ENSG00000174871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:66284660..66284893;chr11:66284661..66284737 26863196 MeRIP-seq:(Medium) rs1290641683 Functional Loss SNV dbSNP153 33..33 33 - - - 57069 RMVar_ID_57069 Human_SNP_ID_470261833 m1A Human chr11 + 66287578 66287578 66287578 GTCCCCCCCGACCCCACCCCACCACGTTCCCCAGCCCAGGTTGGAGACTCACTGGGGATATAGAG GTCCCCCCCGACCCCACCCCACCACGTTCCCCCGCCCAGGTTGGAGACTCACTGGGGATATAGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66287576..66287675 26863196 MeRIP-seq:(Medium) rs752575653 Functional Loss SNV dbSNP153 33..33 33 - - - 57070 RMVar_ID_57070 Human_SNP_ID_470261857 m1A Human chr11 + 66287624 66287624 66287624 ACTCACTGGGGATATAGAGGTCAGGGGCGTTGAGGTCTTGCCGGGGGGGCAGAGGAGCATCACGA ACTCACTGGGGATATAGAGGTCAGGGGCGTTGGGGTCTTGCCGGGGGGGCAGAGGAGCATCACGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66287601..66287625 32194978 MeRIP-seq:(Medium) rs201573906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1354935 57071 RMVar_ID_57071 Human_SNP_ID_470261896 m1A Human chr11 + 66287666 66287666 66287666 GGGGGGGCAGAGGAGCATCACGACTGTACTGCACTTCCCAGTTCTGGCAGTGGCAGTGGCAGCAG GGGGGGGCAGAGGAGCATCACGACTGTACTGCCCTTCCCAGTTCTGGCAGTGGCAGTGGCAGCAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:66287615..66287965 32194978 MeRIP-seq:(Medium) rs775427224 Functional Loss SNV dbSNP153 33..33 33 - - - 57072 RMVar_ID_57072 Human_SNP_ID_470262107 m1A Human chr11 - 66288201 66288201 66288201 GGTGGTTATTCCAGCCAGCCCGGGGGATACCCAGCCACAGGAGCAGACGTGGCCTTCAGTGTCAA GGTGGTTATTCCAGCCAGCCCGGGGGATACCCTGCCACAGGAGCAGACGTGGCCTTCAGTGTCAA T A YIF1A Ensembl:ENSG00000174851 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66288151..66288307 26863196 MeRIP-seq:(Medium) rs1166219056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750470,Human_RBP_ID_3939503,Human_RBP_ID_9322223,Human_RBP_ID_22433773,Human_RBP_ID_22754293,Human_RBP_ID_26803821 Human_Splice_Rec_1262122,Human_Splice_Rec_1262136,Human_Splice_Rec_1262162,Human_Splice_Rec_1262172,Human_Splice_Rec_1262180,Human_Splice_Rec_1262186,Human_Splice_Rec_1262190 RMVar_hsa_circ_43495,RMVar_hsa_circ_113317,RMVar_hsa_circ_120267,RMVar_hsa_circ_150872,RMVar_hsa_circ_150873,RMVar_hsa_circ_10107,RMVar_hsa_circ_336820 57073 RMVar_ID_57073 Human_SNP_ID_470262400 m1A Human chr11 - 66289018 66289018 66289018 CCTCATTAGTATTCGTACCCACGAGGCGGCGCAGCGGGCCCTCGGGGACAGCGAGCGTCGCGGCC CCTCATTAGTATTCGTACCCACGAGGCGGCGCGGCGGGCCCTCGGGGACAGCGAGCGTCGCGGCC T C YIF1A Ensembl:ENSG00000174851 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:66288873..66289100 26863196 MeRIP-seq:(Medium) rs377720789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401359,Human_RBP_ID_809011,Human_RBP_ID_4184242,Human_RBP_ID_5314308,Human_RBP_ID_22433774 Human_Splice_Rec_1262113,Human_Splice_Rec_1262121,Human_Splice_Rec_1262135,Human_Splice_Rec_1262151,Human_Splice_Rec_1262161,Human_Splice_Rec_1262171,Human_Splice_Rec_1262179,Human_Splice_Rec_1262185,Human_Splice_Rec_1262189 RMVar_hsa_circ_120267,RMVar_hsa_circ_150873 57074 RMVar_ID_57074 Human_SNP_ID_470274382 m1A Human chr11 + 66332181 66332181 66332181 AACAAGTATCAGACAAAGGTGGTGGCAGACACAGGACAGGGCCCTGGGTGGGGCTTGCTGGCGCT AACAAGTATCAGACAAAGGTGGTGGCAGACACGGGACAGGGCCCTGGGTGGGGCTTGCTGGCGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66332130..66332280 32194978 MeRIP-seq:(Medium) rs1464503767 Functional Loss SNV dbSNP153 33..33 33 - - - 57075 RMVar_ID_57075 Human_SNP_ID_470274449 m1A Human chr11 + 66332372 66332372 66332372 GCTTGACCCTGGCCCCCTTCAGCAGTTGTCTCAGACTGTTCCCGAATGTCCCTGGGGCTGGCTTT GCTTGACCCTGGCCCCCTTCAGCAGTTGTCTCCGACTGTTCCCGAATGTCCCTGGGGCTGGCTTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66332322..66332492 26863196 MeRIP-seq:(Medium) rs1360731013 Functional Loss SNV dbSNP153 33..33 33 - - - 57076 RMVar_ID_57076 Human_SNP_ID_470274473 m1A Human chr11 - 66332427 66332427 66332427 GGCAAGAAGCAGAGGGGAGGAGCAAGGGTGCCAGGGAGATGGGGATGCTGGGGTCAAAGCCAGCC GGCAAGAAGCAGAGGGGAGGAGCAAGGGTGCCGGGGAGATGGGGATGCTGGGGTCAAAGCCAGCC T C RIN1 Ensembl:ENSG00000174791 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66332378..66332479 32194978 MeRIP-seq:(Medium) rs141803315 Functional Loss SNV dbSNP153 33..33 33 - - - 57077 RMVar_ID_57077 Human_SNP_ID_470274484 m1A Human chr11 - 66332460 66332460 66332460 TGTGACAGAGGAGGAGGGCAGTGGGCAGTCAGAGGCAAGAAGCAGAGGGGAGGAGCAAGGGTGCC TGTGACAGAGGAGGAGGGCAGTGGGCAGTCAGTGGCAAGAAGCAGAGGGGAGGAGCAAGGGTGCC T A RIN1 Ensembl:ENSG00000174791 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66332232..66332493 26863196 MeRIP-seq:(Medium) rs770323799 Functional Loss SNV dbSNP153 33..33 33 - - - 57078 RMVar_ID_57078 Human_SNP_ID_470276589 m1A Human chr11 - 66337718 66337718 66337718 GGGCCCTCCCACTCCATCTGGCACTGGCCTGGACTCCTCCTCTGCCCTCCTCGAGGCCTGCACAG GGGCCCTCCCACTCCATCTGGCACTGGCCTGGGCTCCTCCTCTGCCCTCCTCGAGGCCTGCACAG T C BRMS1 Ensembl:ENSG00000174744 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66337669..66337813 26863196 MeRIP-seq:(Medium) rs537215961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26803822,Human_RBP_ID_27205527,Human_RBP_ID_27414831,Human_RBP_ID_27557134 Human_Splice_Rec_1262298 Human_miRNA_ID_2272882 RMVar_hsa_circ_102545,RMVar_hsa_circ_112955,RMVar_hsa_circ_150876,RMVar_hsa_circ_150877 57079 RMVar_ID_57079 Human_SNP_ID_470276657 m1A Human chr11 - 66337864 66337864 66337864 TGCACAGGACCTTGACCCTGCTGTTCACAGCCAGGGGGACCCTCAGAGCAGCTGGCACTGCACCC TGCACAGGACCTTGACCCTGCTGTTCACAGCCGGGGGGACCCTCAGAGCAGCTGGCACTGCACCC T C BRMS1 Ensembl:ENSG00000174744 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66337431..66338327 32194978 MeRIP-seq:(Medium) rs1374268089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1262312,Human_Splice_Rec_1262330,Human_Splice_Rec_1262346,Human_Splice_Rec_1262362 RMVar_hsa_circ_102545,RMVar_hsa_circ_112955,RMVar_hsa_circ_150876,RMVar_hsa_circ_150877 57080 RMVar_ID_57080 Human_SNP_ID_470277631 m1A Human chr11 + 66340885 66340885 66340885 GAGCAGCAGCTTCTCACTCTGGAAGAGGGGGCAATAGCTCAGCAGGACGGATGGGGTGAGGCCAC GAGCAGCAGCTTCTCACTCTGGAAGAGGGGGCGATAGCTCAGCAGGACGGATGGGGTGAGGCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66340878..66340972 26863196 MeRIP-seq:(Medium) rs768546953 Functional Loss SNV dbSNP153 33..33 33 - - - 57081 RMVar_ID_57081 Human_SNP_ID_470277681 m1A Human chr11 - 66341010 66341010 66341010 CTACAAGGGCTTCTGTCTGGATGTGATCAGGAATAAGTACGAATGTGAGCTGCAGGGAGCCAAAC CTACAAGGGCTTCTGTCTGGATGTGATCAGGAGTAAGTACGAATGTGAGCTGCAGGGAGCCAAAC T C BRMS1 Ensembl:ENSG00000174744 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66340866..66341069 26863196 MeRIP-seq:(Medium) rs1312673283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1781641,Human_RBP_ID_19055189,Human_RBP_ID_23516016 Human_Splice_Rec_1262288,Human_Splice_Rec_1262289,Human_Splice_Rec_1262304,Human_Splice_Rec_1262305,Human_Splice_Rec_1262320,Human_Splice_Rec_1262321,Human_Splice_Rec_1262338,Human_Splice_Rec_1262339,Human_Splice_Rec_1262354,Human_Splice_Rec_1262355,Human_Splice_Rec_1262370,Human_Splice_Rec_1262371,Human_Splice_Rec_1262392 Human_miRNA_ID_2022075,Human_miRNA_ID_2260618,Human_miRNA_ID_2263663,Human_miRNA_ID_2266732 RMVar_hsa_circ_2458,RMVar_hsa_circ_102545,RMVar_hsa_circ_150876 57082 RMVar_ID_57082 Human_SNP_ID_470277923 m1A Human chr11 - 66341617 66341617 66341617 TAGCCCTTACTGGCCTCTTGTCCCAGAGATGGATGATGAGGACTATGAGCGACGCCGCAGCGAGT TAGCCCTTACTGGCCTCTTGTCCCAGAGATGGGTGATGAGGACTATGAGCGACGCCGCAGCGAGT T C BRMS1 Ensembl:ENSG00000174744 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66341526..66341664;chr11:66341509..66341977;chr11:66341511..66341977 26863196 MeRIP-seq:(Medium) rs1271273660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752410,Human_RBP_ID_22491647 Human_Splice_Rec_1262284,Human_Splice_Rec_1262285,Human_Splice_Rec_1262300,Human_Splice_Rec_1262301,Human_Splice_Rec_1262316,Human_Splice_Rec_1262317,Human_Splice_Rec_1262334,Human_Splice_Rec_1262335,Human_Splice_Rec_1262350,Human_Splice_Rec_1262351,Human_Splice_Rec_1262366,Human_Splice_Rec_1262367,Human_Splice_Rec_1262382,Human_Splice_Rec_1262383,Human_Splice_Rec_1262388,Human_Splice_Rec_1262389 57083 RMVar_ID_57083 Human_SNP_ID_470278157 m1A Human chr11 - 66342109 66342109 66342109 GAGGAGCGGAGCGGCAGCCAGACAGAGTCAGAAGAGGAGAGCTCCGGTGAGCCCCTACACACACA GAGGAGCGGAGCGGCAGCCAGACAGAGTCAGAGGAGGAGAGCTCCGGTGAGCCCCTACACACACA T C BRMS1 Ensembl:ENSG00000174744 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66341305..66344621 26863196 MeRIP-seq:(Medium) rs749516403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4173646,Human_RBP_ID_23516020 Human_Splice_Rec_1262283,Human_Splice_Rec_1262299,Human_Splice_Rec_1262315,Human_Splice_Rec_1262333,Human_Splice_Rec_1262349,Human_Splice_Rec_1262365,Human_Splice_Rec_1262381,Human_Splice_Rec_1262387 57084 RMVar_ID_57084 Human_SNP_ID_470278868 m1A Human chr11 - 66345042 66345042 66345042 CCGCGCAGCGCCTACGGGAGTCCGGCGGCAGCAGCCGGTACCGGCAACCACGGGCAGCTCTCAGG CCGCGCAGCGCCTACGGGAGTCCGGCGGCAGCGGCCGGTACCGGCAACCACGGGCAGCTCTCAGG T C BRMS1 Ensembl:ENSG00000174744 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66344937..66345100 26863196 MeRIP-seq:(Medium) rs535611200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4173658 Human_Splice_Rec_1262281,Human_Splice_Rec_1262313,Human_Splice_Rec_1262331,Human_Splice_Rec_1262347,Human_Splice_Rec_1262379,Human_Splice_Rec_1262385,Human_Splice_Rec_1262393 57085 RMVar_ID_57085 Human_SNP_ID_470279054 m1A Human chr11 + 66345701 66345699 66345702 GATTGTTAATAATAACAATAATAATAACAACAATAATACTGCGATAATATTAATACTTCACATTT GATTGTTAATAATAACAATAATAATAACAAC___AATACTGCGATAATATTAATACTTCACATTT CAAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66345651..66345735 26863196 MeRIP-seq:(Medium) rs1350839631 Functional Loss DEL dbSNP153 32..34 33 - - - 57086 RMVar_ID_57086 Human_SNP_ID_470279968 m1A Human chr11 + 66348186 66348186 66348186 CTAATCCATTGTGCTTTGCACGCGTGGGTTCGAATCCCATCCTCGTCGGCCCTGTTTTATAGAGG CTAATCCATTGTGCTTTGCACGCGTGGGTTCGGATCCCATCCTCGTCGGCCCTGTTTTATAGAGG A G AP001107.9 Ensembl:ENSG00000255468 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1027124998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29165,Human_RBP_ID_108238,Human_RBP_ID_227439,Human_RBP_ID_401409,Human_RBP_ID_752246,Human_RBP_ID_1063912,Human_RBP_ID_1126486,Human_RBP_ID_1163115,Human_RBP_ID_1354940,Human_RBP_ID_1459498,Human_RBP_ID_1781648,Human_RBP_ID_3378369,Human_RBP_ID_4187099,Human_RBP_ID_5087036,Human_RBP_ID_5092924,Human_RBP_ID_5165709,Human_RBP_ID_5255807,Human_RBP_ID_5273861,Human_RBP_ID_5283399,Human_RBP_ID_5460692,Human_RBP_ID_5490139,Human_RBP_ID_5644387,Human_RBP_ID_6087110,Human_RBP_ID_8064716,Human_RBP_ID_8177092,Human_RBP_ID_8246533,Human_RBP_ID_8356499,Human_RBP_ID_9656003,Human_RBP_ID_11679430,Human_RBP_ID_17111108,Human_RBP_ID_17667646,Human_RBP_ID_17668869,Human_RBP_ID_17799607,Human_RBP_ID_18176277,Human_RBP_ID_18205883,Human_RBP_ID_18433067,Human_RBP_ID_18545255,Human_RBP_ID_18611345,Human_RBP_ID_19055680,Human_RBP_ID_19661682,Human_RBP_ID_22165404,Human_RBP_ID_22791925,Human_RBP_ID_23124689,Human_RBP_ID_23530419,Human_RBP_ID_24461976,Human_RBP_ID_24551112,Human_RBP_ID_26747699,Human_RBP_ID_26754819,Human_RBP_ID_27154416,Human_RBP_ID_27414863 Human_Splice_Rec_1262401 57087 RMVar_ID_57087 Human_SNP_ID_470283881 m1A Human chr11 + 66364352 66364352 66364352 GATGGGCAGCCGGGACCTCTGGGGCACGTGGCACAGCATGAAGAGGGGCACGAACAGGAACCGCA GATGGGCAGCCGGGACCTCTGGGGCACGTGGCGCAGCATGAAGAGGGGCACGAACAGGAACCGCA A G AP001107.9 Ensembl:ENSG00000255468 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66364301..66364389 26863196 MeRIP-seq:(Medium) rs767265439 Functional Loss SNV dbSNP153 33..33 33 - - - 57088 RMVar_ID_57088 Human_SNP_ID_470285289 m1A Human chr11 + 66369095 66369092 66369095 TGATGAAGCAGACGGAGGCCATGGTGATGGAGAAGAAGGGTCCGGGGCTCATGTCCACCTTGACC TGATGAAGCAGACGGAGGCCATGGTGATGG___AGAAGGGTCCGGGGCTCATGTCCACCTTGACC GAGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66369044..66369224 26863196 MeRIP-seq:(Medium) rs777367661 Functional Loss DEL dbSNP153 31..33 33 - - - 57089 RMVar_ID_57089 Human_SNP_ID_470285442 m1A Human chr11 + 66369436 66369436 66369436 CAGCAGGGGCAGCTGGGACAGCAGCGTCACCCAATTGTTGAAGTTGAAGGCATCCTCGGGACCCG CAGCAGGGGCAGCTGGGACAGCAGCGTCACCCGATTGTTGAAGTTGAAGGCATCCTCGGGACCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66369306..66369520 26863196 MeRIP-seq:(Medium) rs768850070 Functional Loss SNV dbSNP153 33..33 33 - - - 57090 RMVar_ID_57090 Human_SNP_ID_470285474 m1A Human chr11 - 66369501 66369501 66369501 GTACTTCCAGGCGCGACTGGCCGGGGCCGGCAACAGCACAGCCAGGATCCTGAGCACCAACCACA GTACTTCCAGGCGCGACTGGCCGGGGCCGGCAGCAGCACAGCCAGGATCCTGAGCACCAACCACA T C SLC29A2 Ensembl:ENSG00000174669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66369318..66369561 26863196 MeRIP-seq:(Medium) rs143010989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865277,Human_RBP_ID_26318854 Human_Splice_Rec_1262412,Human_Splice_Rec_1262436,Human_Splice_Rec_1262456,Human_Splice_Rec_1262478,Human_Splice_Rec_1262500,Human_Splice_Rec_1262522,Human_Splice_Rec_1262546 Human_miRNA_ID_793056,Human_miRNA_ID_2331954,Human_miRNA_ID_2965039 RMVar_hsa_circ_123861,RMVar_hsa_circ_297787,RMVar_hsa_circ_150887,RMVar_hsa_circ_150889,RMVar_hsa_circ_323901 57091 RMVar_ID_57091 Human_SNP_ID_470285593 m1A Human chr11 - 66369907 66369907 66369907 AGAGGAGTGGCAGGCTATGTGCTCTAGAGAGAATGCAGTTGTTCAGCACCTAGGCCAAAGCCTGG AGAGGAGTGGCAGGCTATGTGCTCTAGAGAGAGTGCAGTTGTTCAGCACCTAGGCCAAAGCCTGG T C SLC29A2 Ensembl:ENSG00000174669 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66369903..66370252 26863196 MeRIP-seq:(Medium) rs527595550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21966606 57092 RMVar_ID_57092 Human_SNP_ID_470286076 m1A Human chr11 - 66371591 66371591 66371591 CTTTCACCCCAGGCGCATCCGCCGCGGCGGCCATGGCGCGAGGAGACGCCCCGCGGGACAGGTGA CTTTCACCCCAGGCGCATCCGCCGCGGCGGCCTTGGCGCGAGGAGACGCCCCGCGGGACAGGTGA T A SLC29A2 Ensembl:ENSG00000174669 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66371310..66371895 26863196 MeRIP-seq:(Medium) rs1295027701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940881,Human_RBP_ID_4173823 Human_Splice_Rec_1262409,Human_Splice_Rec_1262432,Human_Splice_Rec_1262433,Human_Splice_Rec_1262453,Human_Splice_Rec_1262475,Human_Splice_Rec_1262496,Human_Splice_Rec_1262497,Human_Splice_Rec_1262519,Human_Splice_Rec_1262542,Human_Splice_Rec_1262543 57093 RMVar_ID_57093 Human_SNP_ID_470286077 m1A Human chr11 - 66371591 66371591 66371591 CTTTCACCCCAGGCGCATCCGCCGCGGCGGCCATGGCGCGAGGAGACGCCCCGCGGGACAGGTGA CTTTCACCCCAGGCGCATCCGCCGCGGCGGCCGTGGCGCGAGGAGACGCCCCGCGGGACAGGTGA T C SLC29A2 Ensembl:ENSG00000174669 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66371310..66371895 26863196 MeRIP-seq:(Medium) rs1295027701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940881,Human_RBP_ID_4173823 Human_Splice_Rec_1262409,Human_Splice_Rec_1262432,Human_Splice_Rec_1262433,Human_Splice_Rec_1262453,Human_Splice_Rec_1262475,Human_Splice_Rec_1262496,Human_Splice_Rec_1262497,Human_Splice_Rec_1262519,Human_Splice_Rec_1262542,Human_Splice_Rec_1262543 57094 RMVar_ID_57094 Human_SNP_ID_470302851 m1A Human chr11 - 66437261 66437261 66437261 CCTGAAGAGCCACTTGTTCCTTCCTCCCAGGGAAAGAGGTGGCAGGCCTGGTGACCTTGAAGCAT CCTGAAGAGCCACTTGTTCCTTCCTCCCAGGGGAAGAGGTGGCAGGCCTGGTGACCTTGAAGCAT T C MRPL11 Ensembl:ENSG00000174547 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:66436908..66438275 32194978 MeRIP-seq:(Medium) rs1426084705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401460,Human_RBP_ID_866001,Human_RBP_ID_4173857,Human_RBP_ID_5111188 Human_Splice_Rec_1262618,Human_Splice_Rec_1262626,Human_Splice_Rec_1262634,Human_Splice_Rec_1262646,Human_Splice_Rec_1262654 RMVar_hsa_circ_71248,RMVar_hsa_circ_374680,RMVar_hsa_circ_150891 57095 RMVar_ID_57095 Human_SNP_ID_470302854 m1A Human chr11 - 66437265 66437265 66437265 AACACCTGAAGAGCCACTTGTTCCTTCCTCCCAGGGAAAGAGGTGGCAGGCCTGGTGACCTTGAA AACACCTGAAGAGCCACTTGTTCCTTCCTCCCGGGGAAAGAGGTGGCAGGCCTGGTGACCTTGAA T C MRPL11 Ensembl:ENSG00000174547 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:66437258..66437371;chr11:66437242..66437354 26863196 MeRIP-seq:(Medium) rs759150857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401460,Human_RBP_ID_866001,Human_RBP_ID_4193776,Human_RBP_ID_5111188 RMVar_hsa_circ_71248 57096 RMVar_ID_57096 Human_SNP_ID_470302861 m1A Human chr11 + 66437276 66437276 66437276 CAGGCCTGCCACCTCTTTCCCTGGGAGGAAGGAACAAGTGGCTCTTCAGGTGTTACTGCTTCCTT CAGGCCTGCCACCTCTTTCCCTGGGAGGAAGGGACAAGTGGCTCTTCAGGTGTTACTGCTTCCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66437272..66437354 26863196 MeRIP-seq:(Medium) rs1002111114 Functional Loss SNV dbSNP153 33..33 33 - - - 57097 RMVar_ID_57097 Human_SNP_ID_470302894 m1A Human chr11 - 66437388 66437388 66437388 GATTGGACAGCCCACTGTTTCCTACTTCCTGAAGGCAGCAGCTGGGATTGAAAAGGGGGCCCGGC GATTGGACAGCCCACTGTTTCCTACTTCCTGAGGGCAGCAGCTGGGATTGAAAAGGGGGCCCGGC T C MRPL11 Ensembl:ENSG00000174547 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66437376..66437400 26863196 MeRIP-seq:(Medium) rs1369407637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322225,Human_RBP_ID_17649758 Human_Splice_Rec_1262616,Human_Splice_Rec_1262617,Human_Splice_Rec_1262624,Human_Splice_Rec_1262625,Human_Splice_Rec_1262632,Human_Splice_Rec_1262633,Human_Splice_Rec_1262644,Human_Splice_Rec_1262645,Human_Splice_Rec_1262652,Human_Splice_Rec_1262653 RMVar_hsa_circ_71248 57098 RMVar_ID_57098 Human_SNP_ID_470303123 m1A Human chr11 - 66438257 66438255 66438257 CACCACTAACCCCCTCTGCTTCCCTCACAGAGAGGCGTTTCCATCAACCAGTTTTGCAAGGAGTT CACCACTAACCCCCTCTGCTTCCCTCACAGAG__GCGTTTCCATCAACCAGTTTTGCAAGGAGTT CCT C MRPL11 Ensembl:ENSG00000174547 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66438151..66438850 26863196 MeRIP-seq:(Medium) rs755492424 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4186072 Human_Splice_Rec_1262614,Human_Splice_Rec_1262615,Human_Splice_Rec_1262622,Human_Splice_Rec_1262623,Human_Splice_Rec_1262630,Human_Splice_Rec_1262631,Human_Splice_Rec_1262642,Human_Splice_Rec_1262643,Human_Splice_Rec_1262650,Human_Splice_Rec_1262651 RMVar_hsa_circ_71248 57099 RMVar_ID_57099 Human_SNP_ID_470303125 m1A Human chr11 - 66438261 66438261 66438261 CTCTCACCACTAACCCCCTCTGCTTCCCTCACAGAGAGGCGTTTCCATCAACCAGTTTTGCAAGG CTCTCACCACTAACCCCCTCTGCTTCCCTCACTGAGAGGCGTTTCCATCAACCAGTTTTGCAAGG T A MRPL11 Ensembl:ENSG00000174547 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66438226..66438275 26863196 MeRIP-seq:(Medium) rs751569201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1262615,Human_Splice_Rec_1262623,Human_Splice_Rec_1262631,Human_Splice_Rec_1262643,Human_Splice_Rec_1262651 57100 RMVar_ID_57100 Human_SNP_ID_470303213 m1A Human chr11 - 66438579 66438579 66438579 CGACGTGGGGGTTGTCTAGGATGGTGGAAGCTAGGACGCGGATGGAGGGCGCTGGCCCTGGAACC CGACGTGGGGGTTGTCTAGGATGGTGGAAGCTGGGACGCGGATGGAGGGCGCTGGCCCTGGAACC T C MRPL11 Ensembl:ENSG00000174547 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66438576..66438850 26863196 MeRIP-seq:(Medium) rs527936840 Functional Loss SNV dbSNP153 33..33 33 - - - 57101 RMVar_ID_57101 Human_SNP_ID_470303235 m1A Human chr11 + 66438635 66438635 66438635 CCCACGTCGGGTTCCCGCCACGGCCGCACCTGACCCAGCACTGGGCCTAGTGGGGGCCCGGGCAT CCCACGTCGGGTTCCCGCCACGGCCGCACCTGGCCCAGCACTGGGCCTAGTGGGGGCCCGGGCAT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:66438626..66438775 26863410 MeRIP-seq:(Medium) rs772574448 Functional Loss SNV dbSNP153 33..33 33 - - - 57102 RMVar_ID_57102 Human_SNP_ID_470303316 m1A Human chr11 - 66438768 66438768 66438768 CTCTTGCTGCTCCCCTGAGGTGAACTGAAGCCAGCAGCCCCGCATCATGTCAAAGCTCGGCCGGG CTCTTGCTGCTCCCCTGAGGTGAACTGAAGCCGGCAGCCCCGCATCATGTCAAAGCTCGGCCGGG T C MRPL11 Ensembl:ENSG00000174547 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66438201..66438850 26863196 MeRIP-seq:(Medium) rs752232426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1459510,Human_RBP_ID_4184250,Human_RBP_ID_5521161,Human_RBP_ID_9321618,Human_RBP_ID_11679790,Human_RBP_ID_22435488,Human_RBP_ID_26803828,Human_RBP_ID_26895324 Human_Splice_Rec_1262621 57103 RMVar_ID_57103 Human_SNP_ID_470309739 m1A Human chr11 + 66466983 66466983 66466983 CCGCCGCAGCGGCCCGGGGCCGAGCAGGGGCTAGGCGGGGAGGGAGCGGCGCCCAGCGGGGCCCG CCGCCGCAGCGGCCCGGGGCCGAGCAGGGGCTGGGCGGGGAGGGAGCGGCGCCCAGCGGGGCCCG A G PELI3 Ensembl:ENSG00000174516 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66466940..66467092 26863196 MeRIP-seq:(Medium) rs1324333700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186077 Human_Splice_Rec_1262665,Human_Splice_Rec_1262675,Human_Splice_Rec_1262687,Human_Splice_Rec_1262699,Human_Splice_Rec_1262709,Human_Splice_Rec_1262717 57104 RMVar_ID_57104 Human_SNP_ID_470311298 m1A Human chr11 + 66473284 66473284 66473284 CACAGAGAACATGATTGACTTCGTGGTAACAGACACGTCCCCTGGAGGAGGGGCTGCCGAGGGCC CACAGAGAACATGATTGACTTCGTGGTAACAGGCACGTCCCCTGGAGGAGGGGCTGCCGAGGGCC A G PELI3 Ensembl:ENSG00000174516 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66472463..66473383 32194978 MeRIP-seq:(Medium) rs758916445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1262660,Human_Splice_Rec_1262670,Human_Splice_Rec_1262682,Human_Splice_Rec_1262694,Human_Splice_Rec_1262706,Human_Splice_Rec_1262712 RMVar_hsa_circ_52890,RMVar_hsa_circ_150892,RMVar_hsa_circ_317814 57105 RMVar_ID_57105 Human_SNP_ID_470312017 m1A Human chr11 - 66475909 66475909 66475909 GGCACATAAGGCCCCACAAGGCGGCAGAGAGGACATTCGCGCTCCTGGGGGCCCCGCTCCCGCCG GGCACATAAGGCCCCACAAGGCGGCAGAGAGGGCATTCGCGCTCCTGGGGGCCCCGCTCCCGCCG T C AP002748.4 Ensembl:ENSG00000255517 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66475895..66475996 32194978 MeRIP-seq:(Medium) rs773310999 Functional Loss SNV dbSNP153 33..33 33 - - - 57106 RMVar_ID_57106 Human_SNP_ID_470313580 m1A Human chr11 + 66482178 66482178 66482178 ATTGGTATGGGGTAAACAACAGCTGTGATGACAGTGATGGTTCTCAGCAGGGCCCATGGCGGACA ATTGGTATGGGGTAAACAACAGCTGTGATGACCGTGATGGTTCTCAGCAGGGCCCATGGCGGACA A C DPP3 Ensembl:ENSG00000254986 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66482176..66482421 26863196 MeRIP-seq:(Medium) rs1200029991 Functional Loss SNV dbSNP153 33..33 33 - - - 57107 RMVar_ID_57107 Human_SNP_ID_470313590 m1A Human chr11 + 66482229 66482229 66482229 GCCCATGGCGGACACCCAGTACATCCTGCCCAATGACATCGGCGTGTCTAGCCTGGACTGCCGTG GCCCATGGCGGACACCCAGTACATCCTGCCCAGTGACATCGGCGTGTCTAGCCTGGACTGCCGTG A G DPP3 Ensembl:ENSG00000254986 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66482222..66482398 26863196 MeRIP-seq:(Medium) rs200777816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4173938,Human_RBP_ID_17799662,Human_RBP_ID_26803829 Human_Splice_Rec_1262744,Human_Splice_Rec_1262778,Human_Splice_Rec_1262812,Human_Splice_Rec_1262846,Human_Splice_Rec_1262864,Human_Splice_Rec_1262872,Human_Splice_Rec_1262916,Human_Splice_Rec_1262924 Human_miRNA_ID_2938628 RMVar_hsa_circ_12336,RMVar_hsa_circ_35150,RMVar_hsa_circ_266471,RMVar_hsa_circ_49300,RMVar_hsa_circ_109976,RMVar_hsa_circ_40236,RMVar_hsa_circ_150893 57108 RMVar_ID_57108 Human_SNP_ID_470313627 m1A Human chr11 + 66482307 66482307 66482307 GCTGTCACCCACAGAGCGCCTCTATGCCTACCACCTGTCCCGTGCCGCCTGGTACGGAGGCCTGG GCTGTCACCCACAGAGCGCCTCTATGCCTACCGCCTGTCCCGTGCCGCCTGGTACGGAGGCCTGG A G DPP3 Ensembl:ENSG00000254986 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:66482219..66482376 26863196 MeRIP-seq:(Medium) rs1272814993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185151 Human_Splice_Rec_1262854 Human_miRNA_ID_2890455 RMVar_hsa_circ_12336,RMVar_hsa_circ_35150,RMVar_hsa_circ_266471,RMVar_hsa_circ_49300,RMVar_hsa_circ_109976,RMVar_hsa_circ_40236,RMVar_hsa_circ_150893 57109 RMVar_ID_57109 Human_SNP_ID_470316450 m1A Human chr11 - 66492840 66492840 66492840 GCGAAGGTGAGAACATCCAGGGAGGTGAAGTCAGGGGTGAGGAACTTGTCCTTCTCAAAGGTTGG GCGAAGGTGAGAACATCCAGGGAGGTGAAGTCGGGGGTGAGGAACTTGTCCTTCTCAAAGGTTGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:66492730..66492875 26863196 MeRIP-seq:(Medium) rs1276514640 Functional Loss SNV dbSNP153 33..33 33 - - - 57110 RMVar_ID_57110 Human_SNP_ID_470316451 m1A Human chr11 - 66492840 66492840 66492840 GCGAAGGTGAGAACATCCAGGGAGGTGAAGTCAGGGGTGAGGAACTTGTCCTTCTCAAAGGTTGG GCGAAGGTGAGAACATCCAGGGAGGTGAAGTCCGGGGTGAGGAACTTGTCCTTCTCAAAGGTTGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:66492730..66492875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 57111 RMVar_ID_57111 Human_SNP_ID_470329146 m1A Human chr11 - 66539820 66539818 66539820 CCTGACCCTCTCTGCTCTTTTATTGCAGGCAGAGTGTCTCTGGCACAGTTTGCCTTGGCCTTCGT CCTGACCCTCTCTGCTCTTTTATTGCAGGCAG__TGTCTCTGGCACAGTTTGCCTTGGCCTTCGT ACT A ZDHHC24 Ensembl:ENSG00000174165 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66539769..66542628 26863196 MeRIP-seq:(Medium) rs1565296083 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1263384 RMVar_hsa_circ_115933,RMVar_hsa_circ_150909,RMVar_hsa_circ_105758,RMVar_hsa_circ_150908 57112 RMVar_ID_57112 Human_SNP_ID_470329150 m1A Human chr11 - 66539820 66539820 66539820 CCTGACCCTCTCTGCTCTTTTATTGCAGGCAGAGTGTCTCTGGCACAGTTTGCCTTGGCCTTCGT CCTGACCCTCTCTGCTCTTTTATTGCAGGCAGTGTGTCTCTGGCACAGTTTGCCTTGGCCTTCGT T A ZDHHC24 Ensembl:ENSG00000174165 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66539769..66542628 26863196 MeRIP-seq:(Medium) rs774385339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1263384 RMVar_hsa_circ_115933,RMVar_hsa_circ_150909,RMVar_hsa_circ_105758,RMVar_hsa_circ_150908 57113 RMVar_ID_57113 Human_SNP_ID_470330182 m1A Human chr11 - 66543856 66543856 66543856 CCTGCTGGGCCGCTGCGTGGGCTTCGGCAACTACCGGCCCTTCCTGTGCCTGCTGCTTCATGCCG CCTGCTGGGCCGCTGCGTGGGCTTCGGCAACTGCCGGCCCTTCCTGTGCCTGCTGCTTCATGCCG T C ZDHHC24 Ensembl:ENSG00000174165 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66542825..66543916 26863196 MeRIP-seq:(Medium) rs1386350378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4174039 Human_miRNA_ID_2100547 RMVar_hsa_circ_115933,RMVar_hsa_circ_150909,RMVar_hsa_circ_363574 57114 RMVar_ID_57114 Human_SNP_ID_470330735 m1A Human chr11 - 66545996 66545996 66545996 GCTCCGACAGCTGGGTGTCCAGGCCATGGGGCAGCCCTGGGCGGCTGGGAGCACGGACGGGGCGC GCTCCGACAGCTGGGTGTCCAGGCCATGGGGCCGCCCTGGGCGGCTGGGAGCACGGACGGGGCGC T G ZDHHC24 Ensembl:ENSG00000174165 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66545784..66546025 26863196 MeRIP-seq:(Medium) rs1325979091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227101,Human_RBP_ID_4174055,Human_RBP_ID_22433791 RMVar_hsa_circ_115933,RMVar_hsa_circ_150909 57115 RMVar_ID_57115 Human_SNP_ID_470345026 m1A Human chr11 - 66593239 66593239 66593239 CCGAAGCCATTCTGGACCCAGTCACCACCCCGAGACGCAGAACTCCTCCGGCGCAGGAGCACCAA CCGAAGCCATTCTGGACCCAGTCACCACCCCGTGACGCAGAACTCCTCCGGCGCAGGAGCACCAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:66593176..66593351;chr11:66593176..66593674 26863196 MeRIP-seq:(Medium) rs369185929 Functional Loss SNV dbSNP153 33..33 33 - - - 57116 RMVar_ID_57116 Human_SNP_ID_470345037 m1A Human chr11 + 66593250 66593250 66593250 GCGCCGGAGGAGTTCTGCGTCTCGGGGTGGTGACTGGGTCCAGAATGGCTTCGGATTCGGGGAAC GCGCCGGAGGAGTTCTGCGTCTCGGGGTGGTGGCTGGGTCCAGAATGGCTTCGGATTCGGGGAAC A G CCS Ensembl:ENSG00000173992 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66593200..66593346 26863196 MeRIP-seq:(Medium) rs1226303520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185154,Human_RBP_ID_18198754,Human_RBP_ID_18205888,Human_RBP_ID_18417188,Human_RBP_ID_22895427 Human_Splice_Rec_1263573,Human_Splice_Rec_1263585,Human_Splice_Rec_1263599,Human_Splice_Rec_1263603,Human_Splice_Rec_1263617,Human_Splice_Rec_1263619,Human_Splice_Rec_1263627 Human_miRNA_ID_2171783 RMVar_hsa_circ_83359,RMVar_hsa_circ_150912 57117 RMVar_ID_57117 Human_SNP_ID_470345058 m1A Human chr11 + 66593298 66593298 66593298 CTTCGGATTCGGGGAACCAGGGGACCCTCTGCACGGTGAGGGTCGAGGCTTCGTGTGGAGCCTCG CTTCGGATTCGGGGAACCAGGGGACCCTCTGCCCGGTGAGGGTCGAGGCTTCGTGTGGAGCCTCG A C CCS Ensembl:ENSG00000173992 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66593265..66599322 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3939515,Human_RBP_ID_4185154,Human_RBP_ID_5110902,Human_RBP_ID_18417188,Human_RBP_ID_18972339,Human_RBP_ID_19052358,Human_RBP_ID_22895427 Human_Splice_Rec_1263573,Human_Splice_Rec_1263585,Human_Splice_Rec_1263599,Human_Splice_Rec_1263603,Human_Splice_Rec_1263617,Human_Splice_Rec_1263619,Human_Splice_Rec_1263627 Human_miRNA_ID_2272884 RMVar_hsa_circ_83359,RMVar_hsa_circ_150912 57118 RMVar_ID_57118 Human_SNP_ID_470345059 m1A Human chr11 + 66593298 66593298 66593298 CTTCGGATTCGGGGAACCAGGGGACCCTCTGCACGGTGAGGGTCGAGGCTTCGTGTGGAGCCTCG CTTCGGATTCGGGGAACCAGGGGACCCTCTGCGCGGTGAGGGTCGAGGCTTCGTGTGGAGCCTCG A G CCS Ensembl:ENSG00000173992 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66593265..66599322 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3939515,Human_RBP_ID_4185154,Human_RBP_ID_5110902,Human_RBP_ID_18417188,Human_RBP_ID_18972339,Human_RBP_ID_19052358,Human_RBP_ID_22895427 Human_Splice_Rec_1263573,Human_Splice_Rec_1263585,Human_Splice_Rec_1263599,Human_Splice_Rec_1263603,Human_Splice_Rec_1263617,Human_Splice_Rec_1263619,Human_Splice_Rec_1263627 Human_miRNA_ID_2272884 RMVar_hsa_circ_83359,RMVar_hsa_circ_150912 57119 RMVar_ID_57119 Human_SNP_ID_470351102 m1A Human chr11 - 66616675 66616675 66616675 CCACCTTCCTGGAGAGCCCGGACCTCTCCTCCAGCGACAGGCAAGACGTCCGAACGACCGGCAGT CCACCTTCCTGGAGAGCCCGGACCTCTCCTCCGGCGACAGGCAAGACGTCCGAACGACCGGCAGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:66616626..66616750 26863196 MeRIP-seq:(Medium) rs370761611 Functional Loss SNV dbSNP153 33..33 33 - - - 57120 RMVar_ID_57120 Human_SNP_ID_470351154 m1A Human chr11 + 66616794 66616794 66616794 TCCGGAGGAGCTGGCAGCCCTCTTTGCGCCCTACGGCACGGTCATGAGCTGCGCCGTCATGAAAC TCCGGAGGAGCTGGCAGCCCTCTTTGCGCCCTTCGGCACGGTCATGAGCTGCGCCGTCATGAAAC A T RBM14,RBM14-RBM4 Ensembl:ENSG00000239306,Ensembl:ENSG00000248643 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:66616626..66616814 26863196 MeRIP-seq:(Medium) rs771161027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227364,Human_RBP_ID_9321619,Human_RBP_ID_9362602,Human_RBP_ID_22034719,Human_RBP_ID_22471269,Human_RBP_ID_23113185,Human_RBP_ID_26317833,Human_RBP_ID_27414958 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 57121 RMVar_ID_57121 Human_SNP_ID_470351330 m1A Human chr11 - 66617217 66617214 66617217 CTTGGTGGACGGTTCCTGGACCGCAGGGGAGGAGGGTGGCTCTACCCAACGCGCCCCCAACACCT CTTGGTGGACGGTTCCTGGACCGCAGGGGAGG___GTGGCTCTACCCAACGCGCCCCCAACACCT CCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:66617166..66617279 26863196 MeRIP-seq:(Medium) rs949083846 Functional Loss DEL dbSNP153 33..35 33 - - - 57122 RMVar_ID_57122 Human_SNP_ID_470351332 m1A Human chr11 - 66617217 66617217 66617217 CTTGGTGGACGGTTCCTGGACCGCAGGGGAGGAGGGTGGCTCTACCCAACGCGCCCCCAACACCT CTTGGTGGACGGTTCCTGGACCGCAGGGGAGGTGGGTGGCTCTACCCAACGCGCCCCCAACACCT T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:66617166..66617279 26863196 MeRIP-seq:(Medium) rs1318799741 Functional Loss SNV dbSNP153 33..33 33 - - - 57123 RMVar_ID_57123 Human_SNP_ID_470354552 m1A Human chr11 + 66628177 66628177 66628177 TTATTGTAGGGCTGGGGATCGAGGATCTGGGCAAAAAATATGACATTTCCAACCAGGGACAAAAT TTATTGTAGGGCTGGGGATCGAGGATCTGGGCGAAAAATATGACATTTCCAACCAGGGACAAAAT A G RBM14,RBM14-RBM4 Ensembl:ENSG00000239306,Ensembl:ENSG00000248643 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:66628126..66628258 26863196 MeRIP-seq:(Medium) rs993050471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1354957,Human_RBP_ID_6087519,Human_RBP_ID_8356664,Human_RBP_ID_11681313,Human_RBP_ID_23516353 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 57124 RMVar_ID_57124 Human_SNP_ID_470354567 m1A Human chr11 + 66628208 66628208 66628208 CAAAAAATATGACATTTCCAACCAGGGACAAAATGGAGGCTTGGGCTTAGTGATGGGTAAATGGA CAAAAAATATGACATTTCCAACCAGGGACAAAGTGGAGGCTTGGGCTTAGTGATGGGTAAATGGA A G RBM14,RBM14-RBM4 Ensembl:ENSG00000239306,Ensembl:ENSG00000248643 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66628159..66628320 26863196 MeRIP-seq:(Medium) rs1157390840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6087522,Human_RBP_ID_9415048,Human_RBP_ID_11681314,Human_RBP_ID_23516355,Human_RBP_ID_27619104 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 57125 RMVar_ID_57125 Human_SNP_ID_470358239 m1A Human chr11 + 66640121 66640121 66640121 GGCCATCAGGGGCCTTGATAACACAGAGTTTCAAGGTGAACCACCCTCTTTGGGTAGAGGGCTGA GGCCATCAGGGGCCTTGATAACACAGAGTTTCGAGGTGAACCACCCTCTTTGGGTAGAGGGCTGA A G RBM14-RBM4,RBM4 Ensembl:ENSG00000248643,Ensembl:ENSG00000173933 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66640104..66640235 26863196 MeRIP-seq:(Medium) rs1284709123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866007,Human_RBP_ID_2277404,Human_RBP_ID_9362606,Human_RBP_ID_19049989,Human_RBP_ID_22034744,Human_RBP_ID_22569593,Human_RBP_ID_23516421,Human_RBP_ID_26318860,Human_RBP_ID_27803708 Human_Splice_Rec_1263689,Human_Splice_Rec_1263695,Human_Splice_Rec_1263699,Human_Splice_Rec_1263705,Human_Splice_Rec_1263711,Human_Splice_Rec_1263715,Human_Splice_Rec_1263721,Human_Splice_Rec_1263727,Human_Splice_Rec_1263731,Human_Splice_Rec_1263735,Human_Splice_Rec_1263739 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921,RMVar_hsa_circ_108873,RMVar_hsa_circ_150922,RMVar_hsa_circ_88084,RMVar_hsa_circ_271212,RMVar_hsa_circ_286015,RMVar_hsa_circ_119833,RMVar_hsa_circ_150923,RMVar_hsa_circ_150924,RMVar_hsa_circ_150925 57126 RMVar_ID_57126 Human_SNP_ID_470359160 m1A Human chr11 - 66643459 66643459 66643459 TCCTAAGCCGGCTGGTGGACAACTGCACGTGCATTCGTTTGCCTTGAAGAAACAGACGCAAGAAG TCCTAAGCCGGCTGGTGGACAACTGCACGTGCGTTCGTTTGCCTTGAAGAAACAGACGCAAGAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:66643451..66644075 32194978 MeRIP-seq:(Medium) rs1159602795 Functional Loss SNV dbSNP153 33..33 33 - - - 57127 RMVar_ID_57127 Human_SNP_ID_470366406 m1A Human chr11 + 66669161 66669161 66669161 TCATTATACTGCTCAGTAAAGTCTGCCACACGACCCGTACGATCTACTGGGCACTCTTTGGACCA TCATTATACTGCTCAGTAAAGTCTGCCACACGCCCCGTACGATCTACTGGGCACTCTTTGGACCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66669110..66669221 26863196 MeRIP-seq:(Medium) rs200192363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11683379 57128 RMVar_ID_57128 Human_SNP_ID_470370265 m1A Human chr11 + 66683399 66683399 66683399 AAGTAATCCATTTTTATCTGCCATCTCTCTCCATTGATTTGTGCTGCCTGCATTTATTGTATTTT AAGTAATCCATTTTTATCTGCCATCTCTCTCCGTTGATTTGTGCTGCCTGCATTTATTGTATTTT A G lnc-RBM4-2 RNACentral:URS0000D5B40A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66683348..66683497 26863196 MeRIP-seq:(Medium) rs1405693949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11683834 57129 RMVar_ID_57129 Human_SNP_ID_470370271 m1A Human chr11 - 66683432 66683431 66683433 GGGCGGTGAGGGCTATGAGACAAGTTAGACACAAAAATACAATAAATGCAGGCAGCACAAATCAA GGGCGGTGAGGGCTATGAGACAAGTTAGACA__AAAATACAATAAATGCAGGCAGCACAAATCAA TTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66683334..66683498 26863196 MeRIP-seq:(Medium) rs1187412570 Functional Loss DEL dbSNP153 32..33 33 - - - 57130 RMVar_ID_57130 Human_SNP_ID_470370849 m1A Human chr11 - 66685746 66685741 66685746 CTGCTGCTAGGGTCTGTTGCCAAGGTCAACCCATCACCAGGAACTGTCACTGGGGACGAGTCCAT CTGCTGCTAGGGTCTGTTGCCAAGGTCAACCC_____CAGGAACTGTCACTGGGGACGAGTCCAT GGTGAT G SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66685696..66685947 32194978 MeRIP-seq:(Medium) rs890404281 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_17232961 Human_miRNA_ID_2877445 RMVar_hsa_circ_87502,RMVar_hsa_circ_106473,RMVar_hsa_circ_150933,RMVar_hsa_circ_150934 57131 RMVar_ID_57131 Human_SNP_ID_470370851 m1A Human chr11 - 66685746 66685746 66685746 CTGCTGCTAGGGTCTGTTGCCAAGGTCAACCCATCACCAGGAACTGTCACTGGGGACGAGTCCAT CTGCTGCTAGGGTCTGTTGCCAAGGTCAACCCTTCACCAGGAACTGTCACTGGGGACGAGTCCAT T A SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66685696..66685947 32194978 MeRIP-seq:(Medium) rs978795925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17232961 Human_miRNA_ID_2877445 RMVar_hsa_circ_87502,RMVar_hsa_circ_106473,RMVar_hsa_circ_150933,RMVar_hsa_circ_150934 57132 RMVar_ID_57132 Human_SNP_ID_470371812 m1A Human chr11 - 66688265 66688263 66688266 GAAGGAGCGAAAGAGAAAGAGGGAGGAGGAGGAGCGGCGGAAACAGCCGCCTGCTCCCGAACCCA GAAGGAGCGAAAGAGAAAGAGGGAGGAGGAG___CGGCGGAAACAGCCGCCTGCTCCCGAACCCA GCTC G SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66688214..66688353 26863196 MeRIP-seq:(Medium) rs752950222 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22709219,Human_RBP_ID_22893429,Human_RBP_ID_24918273,Human_RBP_ID_26320307 Human_Splice_Rec_1263836,Human_Splice_Rec_1263837,Human_Splice_Rec_1263910,Human_Splice_Rec_1263911,Human_Splice_Rec_1263982,Human_Splice_Rec_1263983,Human_Splice_Rec_1264026,Human_Splice_Rec_1264027,Human_Splice_Rec_1264096,Human_Splice_Rec_1264097,Human_Splice_Rec_1264136,Human_Splice_Rec_1264137,Human_Splice_Rec_1264152,Human_Splice_Rec_1264153 RMVar_hsa_circ_70940 57133 RMVar_ID_57133 Human_SNP_ID_470371814 m1A Human chr11 - 66688265 66688265 66688265 GAAGGAGCGAAAGAGAAAGAGGGAGGAGGAGGAGCGGCGGAAACAGCCGCCTGCTCCCGAACCCA GAAGGAGCGAAAGAGAAAGAGGGAGGAGGAGGGGCGGCGGAAACAGCCGCCTGCTCCCGAACCCA T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66688214..66688353 26863196 MeRIP-seq:(Medium) rs1195473923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709219,Human_RBP_ID_22893429,Human_RBP_ID_24918273,Human_RBP_ID_26320307 Human_Splice_Rec_1263836,Human_Splice_Rec_1263837,Human_Splice_Rec_1263910,Human_Splice_Rec_1263911,Human_Splice_Rec_1263982,Human_Splice_Rec_1263983,Human_Splice_Rec_1264026,Human_Splice_Rec_1264027,Human_Splice_Rec_1264096,Human_Splice_Rec_1264097,Human_Splice_Rec_1264136,Human_Splice_Rec_1264137,Human_Splice_Rec_1264152,Human_Splice_Rec_1264153 RMVar_hsa_circ_70940 57134 RMVar_ID_57134 Human_SNP_ID_470371954 m1A Human chr11 - 66688664 66688664 66688664 TGGCCTGGGAGGAGCGATTCTGTGCGCTGGAGAAGCTTACTGCGGTGAGGGACACAGGACCCCGG TGGCCTGGGAGGAGCGATTCTGTGCGCTGGAGCAGCTTACTGCGGTGAGGGACACAGGACCCCGG T G SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66687628..66688714 32194978 MeRIP-seq:(Medium) rs541138596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773765 Human_Splice_Rec_1263835,Human_Splice_Rec_1263909,Human_Splice_Rec_1263981,Human_Splice_Rec_1264024,Human_Splice_Rec_1264025,Human_Splice_Rec_1264095,Human_Splice_Rec_1264135,Human_Splice_Rec_1264151 Clinvar_Rec_161 RMVar_hsa_circ_70940 57135 RMVar_ID_57135 Human_SNP_ID_470373861 m1A Human chr11 + 66694225 66694225 66694225 GCGCCGGCAGCGTTCCCGCATGGGCTGGCACAAGGCCCTGAACTTCTCCTCCACGGCCCTCGAGG GCGCCGGCAGCGTTCCCGCATGGGCTGGCACATGGCCCTGAACTTCTCCTCCACGGCCCTCGAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66694120..66694322;chr11:66694151..66694300 26863196 MeRIP-seq:(Medium) rs1464620111 Functional Loss SNV dbSNP153 33..33 33 - - - 57136 RMVar_ID_57136 Human_SNP_ID_470375462 m1A Human chr11 - 66700646 66700646 66700646 CTCTTCCTACGACAGCGACTGGAGGCCCTGGGAACTGGCTGGGAGGAGCTGGGCCGAATGTGGGA CTCTTCCTACGACAGCGACTGGAGGCCCTGGGTACTGGCTGGGAGGAGCTGGGCCGAATGTGGGA T A SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66700596..66700707 26863196 MeRIP-seq:(Medium) rs768932281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8771323,Human_RBP_ID_9276598 Clinvar_Rec_162,Clinvar_Rec_1134 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 57137 RMVar_ID_57137 Human_SNP_ID_470375463 m1A Human chr11 - 66700646 66700646 66700646 CTCTTCCTACGACAGCGACTGGAGGCCCTGGGAACTGGCTGGGAGGAGCTGGGCCGAATGTGGGA CTCTTCCTACGACAGCGACTGGAGGCCCTGGGGACTGGCTGGGAGGAGCTGGGCCGAATGTGGGA T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66700596..66700707 26863196 MeRIP-seq:(Medium) rs768932281 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8771323,Human_RBP_ID_9276598 Clinvar_Rec_162,Clinvar_Rec_1134 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 57138 RMVar_ID_57138 Human_SNP_ID_470375486 m1A Human chr11 + 66700719 66700701 66700720 GGTCAGCCTGGTCCCGGGTCACCTCCTCGCCCAGGGCTCGCAGCCGGCTATACTCGCTCTGGGCC GGTCAGCCTGGTCCC___________________GGCTCGCAGCCGGCTATACTCGCTCTGGGCC CGGGTCACCTCCTCGCCCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66700672..66700778 26863196 MeRIP-seq:(Medium) rs1445497338 Functional Loss DEL dbSNP153 16..34 33 - - - 57139 RMVar_ID_57139 Human_SNP_ID_470375494 m1A Human chr11 + 66700719 66700719 66700719 GGTCAGCCTGGTCCCGGGTCACCTCCTCGCCCAGGGCTCGCAGCCGGCTATACTCGCTCTGGGCC GGTCAGCCTGGTCCCGGGTCACCTCCTCGCCCCGGGCTCGCAGCCGGCTATACTCGCTCTGGGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66700672..66700778 26863196 MeRIP-seq:(Medium) rs1436588185 Functional Loss SNV dbSNP153 33..33 33 - - - 57140 RMVar_ID_57140 Human_SNP_ID_470375550 m1A Human chr11 - 66700849 66700849 66700849 GCTTGGATGACTTCCAGGCCTGGCTAGGCCGCACTCAGACTGCTGTGGCCTCTGAAGAAGGGCCG GCTTGGATGACTTCCAGGCCTGGCTAGGCCGCGCTCAGACTGCTGTGGCCTCTGAAGAAGGGCCG T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66700799..66700951 26863196 MeRIP-seq:(Medium) rs1259468529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5436785,Human_RBP_ID_8773790,Human_RBP_ID_9276600,Human_RBP_ID_27415069 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 57141 RMVar_ID_57141 Human_SNP_ID_470377039 m1A Human chr11 - 66705386 66705386 66705386 GAGCAGAGCTATGAGGCACTGTGCGAGTTGGCAGCGGCGCGGCGGGCCCGGCTGGAGGAATCACG GAGCAGAGCTATGAGGCACTGTGCGAGTTGGCCGCGGCGCGGCGGGCCCGGCTGGAGGAATCACG T G SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66705243..66705475 26863196 MeRIP-seq:(Medium) rs757681089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1263802,Human_Splice_Rec_1263876,Human_Splice_Rec_1263948,Human_Splice_Rec_1264020,Human_Splice_Rec_1264062,Human_Splice_Rec_1264134 Human_miRNA_ID_3007089 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 57142 RMVar_ID_57142 Human_SNP_ID_470377183 m1A Human chr11 - 66705735 66705735 66705735 TGGTGGAGGCAGACATCGCCGTGCAGGCCGAGAGGGTGCGGGCCGTCAGCGCCTCTGCCCTGCGC TGGTGGAGGCAGACATCGCCGTGCAGGCCGAGGGGGTGCGGGCCGTCAGCGCCTCTGCCCTGCGC T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66705663..66705854;chr11:66705652..66705825 26863196 MeRIP-seq:(Medium) rs771614577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1263801,Human_Splice_Rec_1263875,Human_Splice_Rec_1263947,Human_Splice_Rec_1264019,Human_Splice_Rec_1264061,Human_Splice_Rec_1264133 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 57143 RMVar_ID_57143 Human_SNP_ID_470377658 m1A Human chr11 + 66707494 66707494 66707494 GGGCCCCCTCGACTCTTGATCACTCTTACCCCACCCAGCACGCCTCACTGGTACCTTCATCTCTT GGGCCCCCTCGACTCTTGATCACTCTTACCCCCCCCAGCACGCCTCACTGGTACCTTCATCTCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66707491..66707599 26863196 MeRIP-seq:(Medium) rs1312319996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150940 57144 RMVar_ID_57144 Human_SNP_ID_470377922 m1A Human chr11 - 66708160 66708160 66708160 GGCTGCCATGCGGGAGACCTGGCTCAGCGAGAACCAGCGCCTCGTGTCCCAGGTAGGACTTGAGG GGCTGCCATGCGGGAGACCTGGCTCAGCGAGACCCAGCGCCTCGTGTCCCAGGTAGGACTTGAGG T G SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66705077..66710655 32194978 MeRIP-seq:(Medium) rs1234270484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1263797,Human_Splice_Rec_1263871,Human_Splice_Rec_1263943,Human_Splice_Rec_1264015,Human_Splice_Rec_1264057,Human_Splice_Rec_1264129 RMVar_hsa_circ_53160,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150941,RMVar_hsa_circ_99783 57145 RMVar_ID_57145 Human_SNP_ID_470380757 m1A Human chr11 + 66719255 66719245 66719256 ACGAGGGCTGTTACCATCCTTTCCACTTGCTTATCACCACCTCCAGTGCCAGCCCCTTCCCTGCC ACGAGGGCTGTTACCATCCTTTC___________CACCACCTCCAGTGCCAGCCCCTTCCCTGCC CCACTTGCTTAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66719252..66719364 26863196 MeRIP-seq:(Medium) rs1365908203 Functional Loss DEL dbSNP153 24..34 33 - - - 57146 RMVar_ID_57146 Human_SNP_ID_470383046 m1A Human chr11 - 66727987 66727987 66727987 ACGGGACGGAGAGGGTCCCGTGCCAGCCACACAGGTACCGGGATGAGGGCGGTGGGGGCCAAGGC ACGGGACGGAGAGGGTCCCGTGCCAGCCACACTGGTACCGGGATGAGGGCGGTGGGGGCCAAGGC T A SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66727938..66728102 26863196 MeRIP-seq:(Medium) rs1444477253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1263777 57147 RMVar_ID_57147 Human_SNP_ID_470383056 m1A Human chr11 - 66728030 66728029 66728030 GGGTCCCGGCGGCCGGGGTGAGCCGGGGCGGGAGCAGGCGGGGACGGGACGGAGAGGGTCCCGTG GGGTCCCGGCGGCCGGGGTGAGCCGGGGCGGG_GCAGGCGGGGACGGGACGGAGAGGGTCCCGTG CT C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66727753..66728090 26863196 MeRIP-seq:(Medium) rs1340116737 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9321632,Human_RBP_ID_18417189,Human_RBP_ID_18478029,Human_RBP_ID_21965811 Human_Splice_Rec_1263777 57148 RMVar_ID_57148 Human_SNP_ID_470383063 m1A Human chr11 + 66728044 66728044 66728044 CGTCCCGTCCCCGCCTGCTCCCGCCCCGGCTCACCCCGGCCGCCGGGACCCGACCCCGACCCCGA CGTCCCGTCCCCGCCTGCTCCCGCCCCGGCTCCCCCCGGCCGCCGGGACCCGACCCCGACCCCGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66727967..66728143 26863196 MeRIP-seq:(Medium) rs993985965 Functional Loss SNV dbSNP153 33..33 33 - - - 57149 RMVar_ID_57149 Human_SNP_ID_470383156 m1A Human chr11 + 66728309 66728309 66728309 GCGGGCGGCGGGCGGGCGCTGTCACGGGGCGCAGGCGGCGCGGGGGGCGCGCGGGGCGGGCGGCG GCGGGCGGCGGGCGGGCGCTGTCACGGGGCGCGGGCGGCGCGGGGGGCGCGCGGGGCGGGCGGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:66728222..66728349 26863196 MeRIP-seq:(Medium) rs1324156209 Functional Loss SNV dbSNP153 33..33 33 - - - 57150 RMVar_ID_57150 Human_SNP_ID_470383180 m1A Human chr11 + 66728373 66728353 66728373 GGCGGGGCGCGTGGCGGCGGCGCGCGGGCGCGAGCGGCGGGACTGCGGCGCCGCGGAAGGAGGAC GGCGGGGCGCGTG____________________GCGGCGGGACTGCGGCGCCGCGGAAGGAGGAC GGCGGCGGCGCGCGGGCGCGA G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:66728241..66728431 26863410 MeRIP-seq:(Medium) rs910884247 Functional Loss DEL dbSNP153 14..33 33 - - - 57151 RMVar_ID_57151 Human_SNP_ID_470386785 m1A Human chr11 - 66744394 66744382 66744394 TTCCAGGACCCTTCCCTCGGCCGGGAGGGGCGACGGTAACGGCGCGGGGCTACCAAGCGGGTTCG TTCCAGGACCCTTCCCTCGGCCGGGAGGGGCG____________CGGGGCTACCAAGCGGGTTCG GCGCCGTTACCGT G lnc-SPTBN2-2 RNACentral:URS00008B3E3F lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66744344..66744453 32194978 MeRIP-seq:(Medium) rs1401820185 Functional Loss DEL dbSNP153 33..44 33 - - - 57152 RMVar_ID_57152 Human_SNP_ID_470386836 m1A Human chr11 + 66744540 66744540 66744540 GGAGGAGTCGTGGCCTGGCCTCATTCCCGCTCACCTCCAGCCTTGGCCGCCTCTCGCGGGCTCTT GGAGGAGTCGTGGCCTGGCCTCATTCCCGCTCCCCTCCAGCCTTGGCCGCCTCTCGCGGGCTCTT A C C11orf80 Ensembl:ENSG00000173715 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66744489..66744641 26863196 MeRIP-seq:(Medium) rs183977788 Functional Loss SNV dbSNP153 33..33 33 - - - 57153 RMVar_ID_57153 Human_SNP_ID_470386947 m1A Human chr11 - 66744764 66744764 66744764 CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCACGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCTCGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:66744718..66744847 26863196 MeRIP-seq:(Medium) rs903238296 Functional Loss SNV dbSNP153 33..33 33 - - - 57154 RMVar_ID_57154 Human_SNP_ID_470386948 m1A Human chr11 - 66744764 66744764 66744764 CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCACGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCGCGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:66744718..66744847 26863196 MeRIP-seq:(Medium) rs903238296 Functional Loss SNV dbSNP153 33..33 33 - - - 57155 RMVar_ID_57155 Human_SNP_ID_470386998 m1A Human chr11 + 66744816 66744816 66744816 GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGCGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66744733..66748441 26863196 MeRIP-seq:(Medium) rs1333256924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184254,Human_RBP_ID_5138685,Human_RBP_ID_18416934 57156 RMVar_ID_57156 Human_SNP_ID_470386999 m1A Human chr11 + 66744816 66744816 66744816 GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGGGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66744733..66748441 26863196 MeRIP-seq:(Medium) rs1333256924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184254,Human_RBP_ID_5138685,Human_RBP_ID_18416934 57157 RMVar_ID_57157 Human_SNP_ID_470387083 m1A Human chr11 - 66744851 66744847 66744851 CAGGGAACAGCGGCAACGCCCAGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGCCGCCGCCGCCC CAGGGAACAGCGGCAACGCCCAGTCGAAGGGT____GCCCGCCGCCGCCGCCGCCGCCGCCGCCC CGGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66744746..66745176 26863196 MeRIP-seq:(Medium) rs1165838195 Functional Loss DEL dbSNP153 33..36 33 - - - 57158 RMVar_ID_57158 Human_SNP_ID_470387086 m1A Human chr11 - 66744851 66744851 66744851 CAGGGAACAGCGGCAACGCCCAGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGCCGCCGCCGCCC CAGGGAACAGCGGCAACGCCCAGTCGAAGGGTGCCCGCCCGCCGCCGCCGCCGCCGCCGCCGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66744746..66745176 26863196 MeRIP-seq:(Medium) rs1423186967 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57159 RMVar_ID_57159 Human_SNP_ID_470387087 m1A Human chr11 - 66744851 66744851 66744851 CAGGGAACAGCGGCAACGCCCAGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGCCGCCGCCGCCC CAGGGAACAGCGGCAACGCCCAGTCGAAGGGTCCCCGCCCGCCGCCGCCGCCGCCGCCGCCGCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66744746..66745176 26863196 MeRIP-seq:(Medium) rs1423186967 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57160 RMVar_ID_57160 Human_SNP_ID_470387095 m1A Human chr11 - 66744862 66744862 66744862 TCCATGCCGCGCAGGGAACAGCGGCAACGCCCAGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGC TCCATGCCGCGCAGGGAACAGCGGCAACGCCCTGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66744740..66745254 26863196 MeRIP-seq:(Medium) rs1190189161 Functional Loss SNV dbSNP153 33..33 33 - - - 57161 RMVar_ID_57161 Human_SNP_ID_470387096 m1A Human chr11 - 66744862 66744862 66744862 TCCATGCCGCGCAGGGAACAGCGGCAACGCCCAGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGC TCCATGCCGCGCAGGGAACAGCGGCAACGCCCGGTCGAAGGGTACCCGCCCGCCGCCGCCGCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66744740..66745254 26863196 MeRIP-seq:(Medium) rs1190189161 Functional Loss SNV dbSNP153 33..33 33 - - - 57162 RMVar_ID_57162 Human_SNP_ID_470387108 m1A Human chr11 + 66744899 66744899 66744899 GTTGCCGCTGTTCCCTGCGCGGCATGGAGGGGACGGCCGTGGCCGTGTTCGAGGTGATGCTGGGA GTTGCCGCTGTTCCCTGCGCGGCATGGAGGGGGCGGCCGTGGCCGTGTTCGAGGTGATGCTGGGA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66744747..66748392 26863196 MeRIP-seq:(Medium) rs77662163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184255,Human_RBP_ID_5314320,Human_RBP_ID_8064411,Human_RBP_ID_9414614,Human_RBP_ID_18416934,Human_RBP_ID_18974291,Human_RBP_ID_19049991 Human_Splice_Rec_1264193,Human_Splice_Rec_1264221,Human_Splice_Rec_1264247,Human_Splice_Rec_1264255,Human_Splice_Rec_1264279,Human_Splice_Rec_1264285,Human_Splice_Rec_1264311 57163 RMVar_ID_57163 Human_SNP_ID_470388110 m1A Human chr11 - 66748355 66748355 66748355 TCTCAAAATCTGAAAAGAGCACAATTCAAAGAAAACATAATCTTCTTTAGAAATCACAGTAATAA TCTCAAAATCTGAAAAGAGCACAATTCAAAGACAACATAATCTTCTTTAGAAATCACAGTAATAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66748350..66748429 26863196 MeRIP-seq:(Medium) rs1421832538 Functional Loss SNV dbSNP153 33..33 33 - - - 57164 RMVar_ID_57164 Human_SNP_ID_470410199 m1A Human chr11 - 66840320 66840320 66840320 GGGTGCAAGTTGGGTGAGTTTACTGAGAAAAGAGATCCGTAAGTATGAAGCAGGAGGCAGAGACT GGGTGCAAGTTGGGTGAGTTTACTGAGAAAAGTGATCCGTAAGTATGAAGCAGGAGGCAGAGACT T A lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66840270..66840461 26863196 MeRIP-seq:(Medium) rs1180330465 Functional Loss SNV dbSNP153 33..33 33 - - - 57165 RMVar_ID_57165 Human_SNP_ID_470411040 m1A Human chr11 - 66843158 66843158 66843158 CCTCCTGCAGCCACAGCACGTCCTGCGGGAACAAGGGGGCCCGGGGTGAGGACCTCTCAGCAGCG CCTCCTGCAGCCACAGCACGTCCTGCGGGAACTAGGGGGCCCGGGGTGAGGACCTCTCAGCAGCG T A lnc-PC-2,lnc-PC-2:2 RNACentral:URS0000D5D865,RNACentral:URS0000D5CCCF lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66843152..66843256 26863196 MeRIP-seq:(Medium) rs1399526307 Functional Loss SNV dbSNP153 33..33 33 - - - 57166 RMVar_ID_57166 Human_SNP_ID_470411277 m1A Human chr11 - 66843522 66843457 66843523 CAGCCCGGGGCCCAGGCCGCCCAGCGCCGCCGACTCGGGCGGCCGCTCCGGCCGCGACACCGACA CAGCCCGGGGCCCAGGCCGCCCAGCGCCGCC__________________________________ TGGCGGCGCTGGGCGGGGATGGGCTGCGACTGCTGTCGGTGTCGCGGCCGGAGCGGCCGCCCGAGTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:66843473..66843584;chr11:66843474..66843582 26863196 MeRIP-seq:(Medium) rs1565200778 Functional Loss DEL dbSNP153 32..65 33 - - - 57167 RMVar_ID_57167 Human_SNP_ID_470411331 m1A Human chr11 - 66843532 66843523 66843533 CCCAGCAGCACAGCCCGGGGCCCAGGCCGCCCAGCGCCGCCGACTCGGGCGGCCGCTCCGGCCGC CCCAGCAGCACAGCCCGGGGCCCAGGCCGCC__________GACTCGGGCGGCCGCTCCGGCCGC CGGCGGCGCTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66843489..66843602 26863196 MeRIP-seq:(Medium) rs1165988931 Functional Loss DEL dbSNP153 32..41 33 - - - 57168 RMVar_ID_57168 Human_SNP_ID_470413265 m1A Human chr11 - 66848676 66848676 66848676 CAGCTGCTTACATGTTCATCTCTTGCCAAATAAGGGTCCCCTCCTCACTGGAGACTACAAGTGGT CAGCTGCTTACATGTTCATCTCTTGCCAAATACGGGTCCCCTCCTCACTGGAGACTACAAGTGGT T G PC Ensembl:ENSG00000173599 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:66848626..66848675 26863196 MeRIP-seq:(Medium) rs61890452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9352650,Human_RBP_ID_17649768,Human_RBP_ID_17799920,Human_RBP_ID_18611621 RMVar_hsa_circ_150999,RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_121031,RMVar_hsa_circ_117534,RMVar_hsa_circ_111761,RMVar_hsa_circ_91292,RMVar_hsa_circ_99383,RMVar_hsa_circ_151001,RMVar_hsa_circ_151002,RMVar_hsa_circ_151003,RMVar_hsa_circ_151000,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 57169 RMVar_ID_57169 Human_SNP_ID_470413279 m1A Human chr11 - 66848729 66848729 66848729 ACACCGCCTGCGGTGGTTCATTCCTTTCAGCCATCGTCCTTTCCTCCGGCGGACAGCTGCTTACA ACACCGCCTGCGGTGGTTCATTCCTTTCAGCCGTCGTCCTTTCCTCCGGCGGACAGCTGCTTACA T C PC Ensembl:ENSG00000173599 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66848680..66848880 32194978 MeRIP-seq:(Medium) rs572319723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17649768,Human_RBP_ID_24462042,Human_RBP_ID_27557191 Human_miRNA_ID_256753,Human_miRNA_ID_260545,Human_miRNA_ID_3077912 RMVar_hsa_circ_150999,RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_121031,RMVar_hsa_circ_117534,RMVar_hsa_circ_111761,RMVar_hsa_circ_91292,RMVar_hsa_circ_99383,RMVar_hsa_circ_151001,RMVar_hsa_circ_151002,RMVar_hsa_circ_151003,RMVar_hsa_circ_151000,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 57170 RMVar_ID_57170 Human_SNP_ID_470414129 m1A Human chr11 - 66850865 66850865 66850865 GGCCTGCACCATGCTGGTCAGCTCCCTCCGGGACCGCTTCCCCGACCTCCCACTGCACATCCACA GGCCTGCACCATGCTGGTCAGCTCCCTCCGGGGCCGCTTCCCCGACCTCCCACTGCACATCCACA T C PC Ensembl:ENSG00000173599 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66850815..66850880 26863196 MeRIP-seq:(Medium) rs1266709873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1264568,Human_Splice_Rec_1264612,Human_Splice_Rec_1264652,Human_Splice_Rec_1264694,Human_Splice_Rec_1264742,Human_Splice_Rec_1264784,Human_Splice_Rec_1264830,Human_Splice_Rec_1264880,Human_Splice_Rec_1264922,Human_Splice_Rec_1264948 RMVar_hsa_circ_150999,RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_121031,RMVar_hsa_circ_117534,RMVar_hsa_circ_111761,RMVar_hsa_circ_151001,RMVar_hsa_circ_151000,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 57171 RMVar_ID_57171 Human_SNP_ID_470416046 m1A Human chr11 + 66856696 66856696 66856696 GGGCATGTGTGGGTGTGTTGGGGAGGGTGCCCAGCGACATGTGACAAAGACGCCCGTCTCCGGGA GGGCATGTGTGGGTGTGTTGGGGAGGGTGCCCGGCGACATGTGACAAAGACGCCCGTCTCCGGGA A G LRFN4 Ensembl:ENSG00000173621 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66856501..66859132;chr11:66856526..66858507 26863196 MeRIP-seq:(Medium) rs1316660510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186087,Human_RBP_ID_5139386,Human_RBP_ID_5235086,Human_RBP_ID_9322236,Human_RBP_ID_18478030,Human_RBP_ID_27415105 57172 RMVar_ID_57172 Human_SNP_ID_470416439 m1A Human chr11 - 66857805 66857805 66857805 GCTGAGCGACTCGGACAGGTTCTGGCAGACGCAGGGCAGCGGGCAGGCGGCCGCTCCACTGGCCA GCTGAGCGACTCGGACAGGTTCTGGCAGACGCGGGGCAGCGGGCAGGCGGCCGCTCCACTGGCCA T C PC Ensembl:ENSG00000173599 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66857767..66857883 26863196 MeRIP-seq:(Medium) rs763973426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385340,Human_RBP_ID_8725214 RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 57173 RMVar_ID_57173 Human_SNP_ID_470416572 m1A Human chr11 + 66858133 66858133 66858133 CGTCAATCTGCAGCACCTCATCCTCAGCGGCAACCAGCTGGGCCGCATCGCGCCGGGAGCCTTCG CGTCAATCTGCAGCACCTCATCCTCAGCGGCACCCAGCTGGGCCGCATCGCGCCGGGAGCCTTCG A C LRFN4 Ensembl:ENSG00000173621 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66853382..66860402 32194978 MeRIP-seq:(Medium) rs1240578770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18188316,Human_RBP_ID_27205889,Human_RBP_ID_27415137 RMVar_hsa_circ_106209,RMVar_hsa_circ_151005,RMVar_hsa_circ_266293 57174 RMVar_ID_57174 Human_SNP_ID_470417585 m1A Human chr11 - 66860176 66860176 66860176 AGCTGCCCGTCCATCACACCACACTCTCTTCCAGCCGCTCGGCGCTGCCTCCTACCCCCCGGCAC AGCTGCCCGTCCATCACACCACACTCTCTTCCGGCCGCTCGGCGCTGCCTCCTACCCCCCGGCAC T C PC Ensembl:ENSG00000173599 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:66859992..66860275;chr11:66860071..66860304;chr11:66860072..66860325 26863196 MeRIP-seq:(Medium) rs756573580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 57175 RMVar_ID_57175 Human_SNP_ID_470417592 m1A Human chr11 + 66860184 66860184 66860184 GGGTAGGAGGCAGCGCCGAGCGGCTGGAAGAGAGTGTGGTGTGATGGACGGGCAGCTTCCTGTGT GGGTAGGAGGCAGCGCCGAGCGGCTGGAAGAGTGTGTGGTGTGATGGACGGGCAGCTTCCTGTGT A T LRFN4 Ensembl:ENSG00000173621 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66860076..66860249 26863196 MeRIP-seq:(Medium) rs1490882497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5138690,Human_RBP_ID_27415195 Human_miRNA_ID_1967272 RMVar_hsa_circ_106209,RMVar_hsa_circ_151005,RMVar_hsa_circ_96781,RMVar_hsa_circ_151008 57176 RMVar_ID_57176 Human_SNP_ID_470418801 m1A Human chr11 - 66863890 66863890 66863890 TGGATAATGCTTCCGCCTTCCAAGGAGCCGTCATCTCGCCCCACTACGACTCCCTGCTGGTCAAA TGGATAATGCTTCCGCCTTCCAAGGAGCCGTCTTCTCGCCCCACTACGACTCCCTGCTGGTCAAA T A PC Ensembl:ENSG00000173599 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66863738..66863897 26863196 MeRIP-seq:(Medium) rs1185836518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9363877 Human_Splice_Rec_1264556,Human_Splice_Rec_1264600,Human_Splice_Rec_1264640,Human_Splice_Rec_1264682,Human_Splice_Rec_1264730,Human_Splice_Rec_1264772,Human_Splice_Rec_1264818,Human_Splice_Rec_1264868,Human_Splice_Rec_1264910,Human_Splice_Rec_1264984,Human_Splice_Rec_1265006,Human_Splice_Rec_1265024 Human_miRNA_ID_2065349,Human_miRNA_ID_2703215,Human_miRNA_ID_2934524 RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998,RMVar_hsa_circ_366759 57177 RMVar_ID_57177 Human_SNP_ID_470435968 m1A Human chr11 + 66933954 66933954 66933954 ACTTCCAGCCCTAATGCTCACTACGCCCCACCAGCACACTCCAACATTGCTTCCCAAGTGCTAGG ACTTCCAGCCCTAATGCTCACTACGCCCCACCGGCACACTCCAACATTGCTTCCCAAGTGCTAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66933950..66934191 26863196 MeRIP-seq:(Medium) rs976144838 Functional Loss SNV dbSNP153 33..33 33 - - - 57178 RMVar_ID_57178 Human_SNP_ID_470442067 m1A Human chr11 - 66958189 66958189 66958189 CGCGCGCAAAGGCGGCGCGGGCTCCGCGAGTGACGGCTGGAGGAGACAGCGACGGGCTGTGCGCG CGCGCGCAAAGGCGGCGCGGGCTCCGCGAGTGGCGGCTGGAGGAGACAGCGACGGGCTGTGCGCG T C PC Ensembl:ENSG00000173599 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66958184..66958358 26863196 MeRIP-seq:(Medium) rs1182058577 Functional Loss SNV dbSNP153 33..33 33 - - - 57179 RMVar_ID_57179 Human_SNP_ID_470454343 m1A Human chr11 - 67006847 67006847 67006847 GGATCAGGGTTGGAGAGACCATTATGAGCCCAAGTGCCCTTCAGCTTCCTTTTTCCTTCTCTGCC GGATCAGGGTTGGAGAGACCATTATGAGCCCAGGTGCCCTTCAGCTTCCTTTTTCCTTCTCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67006814..67006906 26863196 MeRIP-seq:(Medium) rs976152034 Functional Loss SNV dbSNP153 33..33 33 - - - 57180 RMVar_ID_57180 Human_SNP_ID_470454406 m1A Human chr11 - 67007093 67007093 67007093 CCAGGTGTTCAGGCGCCCTTAACCCCATCAGGAAGTCCACTCCCTCACCATGCGGCCCACTCCCG CCAGGTGTTCAGGCGCCCTTAACCCCATCAGGCAGTCCACTCCCTCACCATGCGGCCCACTCCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67007043..67007150 26863196 MeRIP-seq:(Medium) rs1236523159 Functional Loss SNV dbSNP153 33..33 33 - - - 57181 RMVar_ID_57181 Human_SNP_ID_470463635 m1A Human chr11 + 67042702 67042702 67042702 CTAATTTAGCCGAAGGAGGGAGAGGCAGAGCCAGATCATGAAGAGCCTGAATGCCGAGGTCAGGA CTAATTTAGCCGAAGGAGGGAGAGGCAGAGCCGGATCATGAAGAGCCTGAATGCCGAGGTCAGGA A G SYT12 Ensembl:ENSG00000173227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67042651..67042841 26863196 MeRIP-seq:(Medium) rs1271894120 Functional Loss SNV dbSNP153 33..33 33 - - - 57182 RMVar_ID_57182 Human_SNP_ID_470465735 m1A Human chr11 - 67050155 67050155 67050155 GGGTAACCAAAGACTGATGCCAGTAGAGGTGCAACAGCCCAGCCCCTCTGCTTCTGGGTGGGAGC GGGTAACCAAAGACTGATGCCAGTAGAGGTGCCACAGCCCAGCCCCTCTGCTTCTGGGTGGGAGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67050105..67050296 26863196 MeRIP-seq:(Medium) rs1474968968 Functional Loss SNV dbSNP153 33..33 33 - - - 57183 RMVar_ID_57183 Human_SNP_ID_470467419 m1A Human chr11 - 67057019 67057019 67057019 AGGCGCGGGGCACTCACCTCGGGGAAGGCCCCATCGGCGAAGACCATCAGCAGCGACGTCTTCCC AGGCGCGGGGCACTCACCTCGGGGAAGGCCCCTTCGGCGAAGACCATCAGCAGCGACGTCTTCCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:67056851..67057100 26863196 MeRIP-seq:(Medium) rs1345003238 Functional Loss SNV dbSNP153 33..33 33 - - - 57184 RMVar_ID_57184 Human_SNP_ID_470467422 m1A Human chr11 - 67057026 67057025 67057026 GAGGCGGAGGCGCGGGGCACTCACCTCGGGGAAGGCCCCATCGGCGAAGACCATCAGCAGCGACG GAGGCGGAGGCGCGGGGCACTCACCTCGGGGA_GGCCCCATCGGCGAAGACCATCAGCAGCGACG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:67056826..67057084;chr11:67056826..67065950 26863196 MeRIP-seq:(Medium) rs1305172513 Functional Loss DEL dbSNP153 33..33 33 - - - 57185 RMVar_ID_57185 Human_SNP_ID_470469730 m1A Human chr11 - 67065887 67065882 67065887 CTCAAACACCGTGGGGGTGTAGCTCTGAGGAGAAGCAGGGCGGGGGAGGGTGTGAGGAGGCTTCG CTCAAACACCGTGGGGGTGTAGCTCTGAGGAG_____GGGCGGGGGAGGGTGTGAGGAGGCTTCG CTGCTT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:67065876..67065975 26863196 MeRIP-seq:(Medium) rs1484111203 Functional Loss DEL dbSNP153 33..37 33 - - - 57186 RMVar_ID_57186 Human_SNP_ID_470469736 m1A Human chr11 - 67065889 67065889 67065889 CGCTCAAACACCGTGGGGGTGTAGCTCTGAGGAGAAGCAGGGCGGGGGAGGGTGTGAGGAGGCTT CGCTCAAACACCGTGGGGGTGTAGCTCTGAGGGGAAGCAGGGCGGGGGAGGGTGTGAGGAGGCTT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:67065876..67065925 26863196 MeRIP-seq:(Medium) rs1193090485 Functional Loss SNV dbSNP153 33..33 33 - - - 57187 RMVar_ID_57187 Human_SNP_ID_470484050 m1A Human chr11 + 67119330 67119330 67119330 TGCTTCAGCGGCTCCTCCTGTGTGAGGGAAACAACACCCCTCCCCGGCAGCGGCGGCGGCGGCGG TGCTTCAGCGGCTCCTCCTGTGTGAGGGAAACTACACCCCTCCCCGGCAGCGGCGGCGGCGGCGG A T KDM2A Ensembl:ENSG00000173120 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67119281..67119393 26863196 MeRIP-seq:(Medium) rs1234225358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4174852,Human_RBP_ID_5460726,Human_RBP_ID_9321636,Human_RBP_ID_18416604 Human_miRNA_ID_2801240,Human_miRNA_ID_3009370 RMVar_hsa_circ_151013,RMVar_hsa_circ_79201 57188 RMVar_ID_57188 Human_SNP_ID_470484059 m1A Human chr11 + 67119346 67119343 67119346 CCTGTGTGAGGGAAACAACACCCCTCCCCGGCAGCGGCGGCGGCGGCGGCGGCTCTCGGAGCACC CCTGTGTGAGGGAAACAACACCCCTCCCCG___GCGGCGGCGGCGGCGGCGGCTCTCGGAGCACC GGCA G KDM2A Ensembl:ENSG00000173120 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:67119304..67119407;chr11:67119301..67119552 26863196 MeRIP-seq:(Medium) rs1053075240 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5460726,Human_RBP_ID_9321636,Human_RBP_ID_18416604 RMVar_hsa_circ_151013,RMVar_hsa_circ_79201 57189 RMVar_ID_57189 Human_SNP_ID_470484063 m1A Human chr11 + 67119346 67119346 67119346 CCTGTGTGAGGGAAACAACACCCCTCCCCGGCAGCGGCGGCGGCGGCGGCGGCTCTCGGAGCACC CCTGTGTGAGGGAAACAACACCCCTCCCCGGCGGCGGCGGCGGCGGCGGCGGCTCTCGGAGCACC A G KDM2A Ensembl:ENSG00000173120 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:67119304..67119407;chr11:67119301..67119552 26863196 MeRIP-seq:(Medium) rs1009246817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5460726,Human_RBP_ID_9321636,Human_RBP_ID_18416604 RMVar_hsa_circ_151013,RMVar_hsa_circ_79201 57190 RMVar_ID_57190 Human_SNP_ID_470518804 m1A Human chr11 - 67250679 67250679 67250679 TGCATCCAGCTTTCGTCTCCATCCTGAGCCCAACTGCCCCGGCCATTCAGCCTGGCTGCACCCCC TGCATCCAGCTTTCGTCTCCATCCTGAGCCCAGCTGCCCCGGCCATTCAGCCTGGCTGCACCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:67250585..67250825;chr11:67250569..67250804 26863196 MeRIP-seq:(Medium) rs1221118068 Functional Loss SNV dbSNP153 33..33 33 - - - 57191 RMVar_ID_57191 Human_SNP_ID_470520063 m1A Human chr11 - 67255531 67255531 67255531 GGGACTCCTGGGGCTGCTGGCCCCTCCTGCGCAAGCCGGGAGAGTGTGATGGAGGAGAGACGCGC GGGACTCCTGGGGCTGCTGGCCCCTCCTGCGCGAGCCGGGAGAGTGTGATGGAGGAGAGACGCGC T C AP001885.3 Ensembl:ENSG00000287934 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67255483..67255645 26863196 MeRIP-seq:(Medium) rs1213727272 Functional Loss SNV dbSNP153 33..33 33 - - - 57192 RMVar_ID_57192 Human_SNP_ID_470522883 m1A Human chr11 + 67266641 67266641 67266641 AGCGAGCCGCGGCCGGGCCGGGCCGAGCGCCGAGCGAGCAGGAGCGGCGGCGGCGGCGGCGGCGG AGCGAGCCGCGGCCGGGCCGGGCCGAGCGCCGGGCGAGCAGGAGCGGCGGCGGCGGCGGCGGCGG A G GRK2 Ensembl:ENSG00000173020 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67266405..67266848 26863196 MeRIP-seq:(Medium) rs1261056751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867888,Human_RBP_ID_4184261 Human_miRNA_ID_2017847 RMVar_hsa_circ_127619,RMVar_hsa_circ_151036 57193 RMVar_ID_57193 Human_SNP_ID_470526530 m1A Human chr11 + 67279518 67279518 67279518 ATACATCATGAAGGAGCTGCTGGCCTGCTCGCATGTGAGTGTCCTCAGCTGGCCCTGTGTGCTGG ATACATCATGAAGGAGCTGCTGGCCTGCTCGCGTGTGAGTGTCCTCAGCTGGCCCTGTGTGCTGG A G GRK2 Ensembl:ENSG00000173020 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67277276..67280236 32194978 MeRIP-seq:(Medium) rs529567037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867893,Human_RBP_ID_9363899,Human_RBP_ID_17805262,Human_RBP_ID_18410648,Human_RBP_ID_18972357,Human_RBP_ID_19052403 Human_Splice_Rec_1265375,Human_Splice_Rec_1265415,Human_Splice_Rec_1265445,Human_Splice_Rec_1265473 RMVar_hsa_circ_6765,RMVar_hsa_circ_127619,RMVar_hsa_circ_151036,RMVar_hsa_circ_13279,RMVar_hsa_circ_356572,RMVar_hsa_circ_4602,RMVar_hsa_circ_359863,RMVar_hsa_circ_323904 57194 RMVar_ID_57194 Human_SNP_ID_470528517 m1A Human chr11 + 67285440 67285440 67285440 CAAGGTGCCGCTGGTCCAGCGCGGCAGTGCCAACGGCCTCTGACCCGCCCACCCGCCTTTTATAA CAAGGTGCCGCTGGTCCAGCGCGGCAGTGCCAGCGGCCTCTGACCCGCCCACCCGCCTTTTATAA A G GRK2 Ensembl:ENSG00000173020 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67285392..67285712 26863196 MeRIP-seq:(Medium) rs759325066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11687070,Human_RBP_ID_27415324 57195 RMVar_ID_57195 Human_SNP_ID_470528844 m1A Human chr11 - 67286435 67286435 67286435 TGAGTAGACGGGAGGGGAGGGTGCGCCAACCCAGCCCCGGGGGGGAGAAGGCGCGACACCACACA TGAGTAGACGGGAGGGGAGGGTGCGCCAACCCGGCCCCGGGGGGGAGAAGGCGCGACACCACACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67286046..67286500 26863196 MeRIP-seq:(Medium) rs1167352155 Functional Loss SNV dbSNP153 33..33 33 - - - 57196 RMVar_ID_57196 Human_SNP_ID_470529992 m1A Human chr11 - 67290085 67290085 67290085 GTGGGGTCCGCCCGCGGGGGTCCTCCTGTTCAATGTCGTGCTGGGGGAGACGGGACACTCACAAA GTGGGGTCCGCCCGCGGGGGTCCTCCTGTTCAGTGTCGTGCTGGGGGAGACGGGACACTCACAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67290063..67290169 26863196 MeRIP-seq:(Medium) rs1409335527 Functional Loss SNV dbSNP153 33..33 33 - - - 57197 RMVar_ID_57197 Human_SNP_ID_470529993 m1A Human chr11 - 67290085 67290085 67290085 GTGGGGTCCGCCCGCGGGGGTCCTCCTGTTCAATGTCGTGCTGGGGGAGACGGGACACTCACAAA GTGGGGTCCGCCCGCGGGGGTCCTCCTGTTCACTGTCGTGCTGGGGGAGACGGGACACTCACAAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67290063..67290169 26863196 MeRIP-seq:(Medium) rs1409335527 Functional Loss SNV dbSNP153 33..33 33 - - - 57198 RMVar_ID_57198 Human_SNP_ID_470534084 m1A Human chr11 - 67303627 67303627 67303627 CCGGGGGCGAACGGCTCACTGTGACCAGGGCCATGGAGCCAGGCCGCGAGCACCTGGGCTGGCAC CCGGGGGCGAACGGCTCACTGTGACCAGGGCCGTGGAGCCAGGCCGCGAGCACCTGGGCTGGCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:67303579..67303735;chr11:67303578..67303765 26863196 MeRIP-seq:(Medium) rs903288284 Functional Loss SNV dbSNP153 33..33 33 - - - 57199 RMVar_ID_57199 Human_SNP_ID_470534530 m1A Human chr11 + 67304828 67304828 67304828 GGGCTGTCCTGGGACTGCAGGATGGAGGGGACAATGATGATGCAGCAGAGGCCAGTTCTGAGCCA GGGCTGTCCTGGGACTGCAGGATGGAGGGGACGATGATGATGCAGCAGAGGCCAGTTCTGAGCCA A G SSH3 Ensembl:ENSG00000172830 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67304750..67304925 26863196 MeRIP-seq:(Medium) rs1266442968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17800031 Human_Splice_Rec_1265730,Human_Splice_Rec_1265754,Human_Splice_Rec_1265770,Human_Splice_Rec_1265778,Human_Splice_Rec_1265804,Human_Splice_Rec_1265828,Human_Splice_Rec_1265830 RMVar_hsa_circ_352631 57200 RMVar_ID_57200 Human_SNP_ID_470536666 m1A Human chr11 + 67311757 67311750 67311757 CCAGGGCAGTGCCGTGGTGGCCAACCGGACCCAGGCCTTCCAGGAGCAGGAGCAGGGGCAGGGGC CCAGGGCAGTGCCGTGGTGGCCAACC_______GGCCTTCCAGGAGCAGGAGCAGGGGCAGGGGC CGGACCCA C SSH3 Ensembl:ENSG00000172830 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67311708..67311909 32194978 MeRIP-seq:(Medium) rs958331266 Functional Loss DEL dbSNP153 27..33 33 - - - 57201 RMVar_ID_57201 Human_SNP_ID_470536854 m1A Human chr11 - 67312282 67312282 67312282 CCAGGAATGAACTGGGAGAGGACAGGAGGTGCAGGGAGGGGGCGGGGGTGGGAGGCGTGACCCTT CCAGGAATGAACTGGGAGAGGACAGGAGGTGCGGGGAGGGGGCGGGGGTGGGAGGCGTGACCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67312231..67312425 26863196 MeRIP-seq:(Medium) rs1384570887 Functional Loss SNV dbSNP153 33..33 33 - - - 57202 RMVar_ID_57202 Human_SNP_ID_470538197 m1A Human chr11 - 67317908 67317908 67317908 ACCGGGTCCCAGCCCCAGCGCACCTCAGGAAGAAACAACACCTTCGCGCTTAGCTGAGTCAAGCG ACCGGGTCCCAGCCCCAGCGCACCTCAGGAAGGAACAACACCTTCGCGCTTAGCTGAGTCAAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67317877..67318034 26863196 MeRIP-seq:(Medium) rs1024814595 Functional Loss SNV dbSNP153 33..33 33 - - - 57203 RMVar_ID_57203 Human_SNP_ID_470546419 m1A Human chr11 - 67352754 67352754 67352754 GCGCTGGTGTCGGGCCAAGCAGATGGGCTTGGAGCCTCCCCCAGAGGTGTGGCAGGTGCTGAAGA GCGCTGGTGTCGGGCCAAGCAGATGGGCTTGGTGCCTCCCCCAGAGGTGTGGCAGGTGCTGAAGA T A POLD4,AP003419.1 Ensembl:ENSG00000175482,Ensembl:ENSG00000256514 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67351625..67353175 32194978 MeRIP-seq:(Medium) rs774791582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808656,Human_RBP_ID_22433134 Human_Splice_Rec_1265982,Human_Splice_Rec_1265983,Human_Splice_Rec_1265988,Human_Splice_Rec_1265989,Human_Splice_Rec_1265991,Human_Splice_Rec_1265996,Human_Splice_Rec_1265997,Human_Splice_Rec_1266002,Human_Splice_Rec_1266003,Human_Splice_Rec_1266016,Human_Splice_Rec_1266017,Human_Splice_Rec_1266020,Human_Splice_Rec_1266022,Human_Splice_Rec_1266028,Human_Splice_Rec_1266029 Human_miRNA_ID_2424497,Human_miRNA_ID_2434159 RMVar_hsa_circ_97497,RMVar_hsa_circ_115043,RMVar_hsa_circ_151048,RMVar_hsa_circ_151049 57204 RMVar_ID_57204 Human_SNP_ID_470546493 m1A Human chr11 + 67352956 67352956 67352956 ACTTCAGAGACGTGTGGGTGACTGGCTGGGAGAGGCGCCTCCGTGGGGCTGGGTGGGTTCTCACC ACTTCAGAGACGTGTGGGTGACTGGCTGGGAGGGGCGCCTCCGTGGGGCTGGGTGGGTTCTCACC A G RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:67352952..67353087 26863196 MeRIP-seq:(Medium) rs760265088 Functional Loss SNV dbSNP153 33..33 33 - - - 57205 RMVar_ID_57205 Human_SNP_ID_470546494 m1A Human chr11 + 67352956 67352956 67352956 ACTTCAGAGACGTGTGGGTGACTGGCTGGGAGAGGCGCCTCCGTGGGGCTGGGTGGGTTCTCACC ACTTCAGAGACGTGTGGGTGACTGGCTGGGAGTGGCGCCTCCGTGGGGCTGGGTGGGTTCTCACC A T RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:67352952..67353087 26863196 MeRIP-seq:(Medium) rs760265088 Functional Loss SNV dbSNP153 33..33 33 - - - 57206 RMVar_ID_57206 Human_SNP_ID_470549648 m1A Human chr11 + 67366221 67366221 67366221 GAAGTGAGTGGGTGGAGAGGAAGTGGAGGCAGAGGGTGTAGACCACTCCTTGGAGAAATTTGGCA GAAGTGAGTGGGTGGAGAGGAAGTGGAGGCAGTGGGTGTAGACCACTCCTTGGAGAAATTTGGCA A T RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67366218..67366333 26863196 MeRIP-seq:(Medium) rs1415300831 Functional Loss SNV dbSNP153 33..33 33 - - - 57207 RMVar_ID_57207 Human_SNP_ID_470556421 m1A Human chr11 - 67392017 67392017 67392017 TTCATGCTGCCCCAGCGCTCCGCCAGCGGCCAACACTGCCCAGCTCTCCGCGACCTCCGGGTCCG TTCATGCTGCCCCAGCGCTCCGCCAGCGGCCAGCACTGCCCAGCTCTCCGCGACCTCCGGGTCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67391968..67392732 26863196 MeRIP-seq:(Medium) rs1380053828 Functional Loss SNV dbSNP153 33..33 33 - - - 57208 RMVar_ID_57208 Human_SNP_ID_470558865 m1A Human chr11 - 67398525 67398525 67398525 ATTCCGCCAAAGCCAAGAAATAGCCCCCGCACACCACCCTGTGCCCCAGATGATGGATTGATTGT ATTCCGCCAAAGCCAAGAAATAGCCCCCGCACGCCACCCTGTGCCCCAGATGATGGATTGATTGT T C PPP1CA Ensembl:ENSG00000172531 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:67398476..67398525 26863196 MeRIP-seq:(Medium) rs769692389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401979,Human_RBP_ID_4175256,Human_RBP_ID_11687436,Human_RBP_ID_17350266,Human_RBP_ID_17649772,Human_RBP_ID_21883084,Human_RBP_ID_23517092,Human_RBP_ID_26804963,Human_RBP_ID_27415377 57209 RMVar_ID_57209 Human_SNP_ID_470559268 m1A Human chr11 - 67399562 67399562 67399562 ATAGTGGACGAAAAGATCTTCTGCTGCCACGGAGGTGAGGGAGGGGATGGCTGGGGAGGAGGAGC ATAGTGGACGAAAAGATCTTCTGCTGCCACGGCGGTGAGGGAGGGGATGGCTGGGGAGGAGGAGC T G PPP1CA Ensembl:ENSG00000172531 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:67399551..67399600 26863196 MeRIP-seq:(Medium) rs894476377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19050059,Human_RBP_ID_22434670 Human_Splice_Rec_1266047,Human_Splice_Rec_1266059,Human_Splice_Rec_1266071,Human_Splice_Rec_1266081,Human_Splice_Rec_1266091,Human_Splice_Rec_1266097,Human_Splice_Rec_1266115 57210 RMVar_ID_57210 Human_SNP_ID_470559981 m1A Human chr11 - 67401710 67401710 67401710 GGCGCCTGCTGGAAGGTTGGTCGGGGCGGGGGAGGCCCGCGTCCGCCGCGCCCTGGCCCCCTGCC GGCGCCTGCTGGAAGGTTGGTCGGGGCGGGGGGGGCCCGCGTCCGCCGCGCCCTGGCCCCCTGCC T C PPP1CA Ensembl:ENSG00000172531 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67401704..67401850 26863410 MeRIP-seq:(Medium) rs1038855516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19052453 57211 RMVar_ID_57211 Human_SNP_ID_470560032 m1A Human chr11 + 67401808 67401794 67401808 CGGACATGGCGGCGCCGCCGCTCCAGCCCAGCAGCTCCTGGCCCGCTCCTGCCTCCCGCCCTCCG CGGACATGGCGGCGCCGCC______________GCTCCTGGCCCGCTCCTGCCTCCCGCCCTCCG CGCTCCAGCCCAGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:67401600..67401875;chr11:67401600..67401900;chr11:67401680..67401875 26863196 MeRIP-seq:(Medium) rs1303829363 Functional Loss DEL dbSNP153 20..33 33 - - - 57212 RMVar_ID_57212 Human_SNP_ID_470564166 m1A Human chr11 + 67415393 67415389 67415394 ATGGCAGCCCTACGTCTGTGACCCTCGACGACAGTCCCTGTCCATCTGTACCTGGCCCTCTGTCG ATGGCAGCCCTACGTCTGTGACCCTCGAC_____TCCCTGTCCATCTGTACCTGGCCCTCTGTCG CGACAG C CARNS1 Ensembl:ENSG00000172508 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67415241..67415500 26863196 MeRIP-seq:(Medium) rs979393048 Functional Loss DEL dbSNP153 30..34 33 - - - Human_Splice_Rec_1266222 57213 RMVar_ID_57213 Human_SNP_ID_470564178 m1A Human chr11 - 67415413 67415413 67415413 CAGAGACACAGAGGAAGTCCCGACAGAGGGCCAGGTACAGATGGACAGGGACTGTCGTCGAGGGT CAGAGACACAGAGGAAGTCCCGACAGAGGGCCTGGTACAGATGGACAGGGACTGTCGTCGAGGGT T A PPP1CA Ensembl:ENSG00000172531 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67415235..67415504 26863196 MeRIP-seq:(Medium) rs1345679561 Functional Loss SNV dbSNP153 33..33 33 - - - 57214 RMVar_ID_57214 Human_SNP_ID_470566052 m1A Human chr11 - 67420797 67420797 67420797 GTGTGCGCCCGGCGCCCGCCGCGCTGCTCGGCACTCAGGCCGGCCTCCAGAGCCAGCACGGCGGC GTGTGCGCCCGGCGCCCGCCGCGCTGCTCGGCGCTCAGGCCGGCCTCCAGAGCCAGCACGGCGGC T C PPP1CA Ensembl:ENSG00000172531 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67420792..67420875 26863196 MeRIP-seq:(Medium) rs1311072989 Functional Loss SNV dbSNP153 33..33 33 - - - 57215 RMVar_ID_57215 Human_SNP_ID_470566317 m1A Human chr11 - 67421358 67421358 67421358 CTTACTCCTGGGCTTACTTGTACCTGGCCAGGATGCCCCGCCCAAGCACCGCCTCTAGCGCGGCT CTTACTCCTGGGCTTACTTGTACCTGGCCAGGGTGCCCCGCCCAAGCACCGCCTCTAGCGCGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67421351..67421527 26863196 MeRIP-seq:(Medium) rs368105354 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_163 57216 RMVar_ID_57216 Human_SNP_ID_470568464 m1A Human chr11 + 67428521 67428521 67428521 CTGTCAGTCAGTGCGCGGCCAGGTACGGGCCGACGGGCCCGCGGGGCCGGCGCCGCCATGGCGGC CTGTCAGTCAGTGCGCGGCCAGGTACGGGCCGGCGGGCCCGCGGGGCCGGCGCCGCCATGGCGGC A G RPS6KB2 Ensembl:ENSG00000175634 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67428476..67428668 26863196 MeRIP-seq:(Medium) rs1217021887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184264,Human_RBP_ID_5111204,Human_RBP_ID_18417193 57217 RMVar_ID_57217 Human_SNP_ID_470568489 m1A Human chr11 + 67428546 67428546 67428546 CGGGCCGACGGGCCCGCGGGGCCGGCGCCGCCATGGCGGCCGTGTTTGATTTGGATTTGGAGACG CGGGCCGACGGGCCCGCGGGGCCGGCGCCGCCGTGGCGGCCGTGTTTGATTTGGATTTGGAGACG A G RPS6KB2 Ensembl:ENSG00000175634 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67428501..67428657 26863196 MeRIP-seq:(Medium) rs1009899378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402002,Human_RBP_ID_4184264,Human_RBP_ID_5111204,Human_RBP_ID_18417193 Human_Splice_Rec_1266303,Human_Splice_Rec_1266309,Human_Splice_Rec_1266325,Human_Splice_Rec_1266333,Human_Splice_Rec_1266345,Human_Splice_Rec_1266371,Human_Splice_Rec_1266379 57218 RMVar_ID_57218 Human_SNP_ID_470568490 m1A Human chr11 - 67428547 67428547 67428547 CCGTCTCCAAATCCAAATCAAACACGGCCGCCATGGCGGCGCCGGCCCCGCGGGCCCGTCGGCCC CCGTCTCCAAATCCAAATCAAACACGGCCGCCGTGGCGGCGCCGGCCCCGCGGGCCCGTCGGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67428476..67428694 26863196 MeRIP-seq:(Medium) rs372357474 Functional Loss SNV dbSNP153 33..33 33 - - - 57219 RMVar_ID_57219 Human_SNP_ID_470568571 m1A Human chr11 + 67428709 67428709 67428709 CCGAGGCCGGAGCGGCGGCTCCGCACGCCCAGAGCGGGCTCCGACTCTTTGCAGACCCAGATCCT CCGAGGCCGGAGCGGCGGCTCCGCACGCCCAGCGCGGGCTCCGACTCTTTGCAGACCCAGATCCT A C RPS6KB2 Ensembl:ENSG00000175634 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67428708..67428808 32194978 MeRIP-seq:(Medium) rs1242319061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22895440 57220 RMVar_ID_57220 Human_SNP_ID_470568707 m1A Human chr11 + 67429054 67429054 67429054 AGTGAGTGAGGGTCGTGTTGGGGGAGGGGGGAATGGAGTGGGGAAGGGGAACTGGGGAGCACTGG AGTGAGTGAGGGTCGTGTTGGGGGAGGGGGGACTGGAGTGGGGAAGGGGAACTGGGGAGCACTGG A C RPS6KB2 Ensembl:ENSG00000175634 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67429052..67429145 26863196 MeRIP-seq:(Medium) rs779561932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5342788,Human_RBP_ID_9415057,Human_RBP_ID_22644370,Human_RBP_ID_26776507 Human_Splice_Rec_1266310,Human_Splice_Rec_1266334,Human_Splice_Rec_1266346,Human_Splice_Rec_1266380 RMVar_hsa_circ_96866,RMVar_hsa_circ_151057 57221 RMVar_ID_57221 Human_SNP_ID_470568758 m1A Human chr11 + 67429177 67429177 67429177 GAGCTGACTGAGACCAGCGTGAACGTTGGCCCAGAGCGCATCGGGCCCCACTGCTTTGAGCTGCT GAGCTGACTGAGACCAGCGTGAACGTTGGCCCGGAGCGCATCGGGCCCCACTGCTTTGAGCTGCT A G RPS6KB2 Ensembl:ENSG00000175634 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67429035..67429192 26863196 MeRIP-seq:(Medium) rs1274279758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186105,Human_RBP_ID_5110545,Human_RBP_ID_5344131,Human_RBP_ID_9362628,Human_RBP_ID_18972393,Human_RBP_ID_23517107 Human_Splice_Rec_1266304,Human_Splice_Rec_1266305,Human_Splice_Rec_1266312,Human_Splice_Rec_1266313,Human_Splice_Rec_1266328,Human_Splice_Rec_1266329,Human_Splice_Rec_1266336,Human_Splice_Rec_1266337,Human_Splice_Rec_1266348,Human_Splice_Rec_1266349,Human_Splice_Rec_1266372,Human_Splice_Rec_1266373,Human_Splice_Rec_1266382,Human_Splice_Rec_1266383,Human_Splice_Rec_1266407 Human_miRNA_ID_2424498,Human_miRNA_ID_2434160 RMVar_hsa_circ_96866,RMVar_hsa_circ_151057 57222 RMVar_ID_57222 Human_SNP_ID_470572021 m1A Human chr11 + 67438298 67438298 67438298 TGCGCTGCCTCAGAGGCTCTGGGCAGCCAGCTAGCCCGGTGCGACCCGCTGGCAGAAGCTGAGTG TGCGCTGCCTCAGAGGCTCTGGGCAGCCAGCTGGCCCGGTGCGACCCGCTGGCAGAAGCTGAGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67438097..67438297 32194978 MeRIP-seq:(Medium) rs1019622632 Functional Loss SNV dbSNP153 33..33 33 - - - 57223 RMVar_ID_57223 Human_SNP_ID_470572126 m1A Human chr11 - 67438482 67438482 67438482 CATGTCCCCACAGGAGGCTGGGAAGCTGGAGGAGGTGATGCAGGAGCTGCGGGCCCTGAGGGCGC CATGTCCCCACAGGAGGCTGGGAAGCTGGAGGTGGTGATGCAGGAGCTGCGGGCCCTGAGGGCGC T A CORO1B Ensembl:ENSG00000172725 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67438168..67438509 26863196 MeRIP-seq:(Medium) rs1565152084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5490188,Human_RBP_ID_17648458,Human_RBP_ID_18188323,Human_RBP_ID_22433806 Human_Splice_Rec_1266482,Human_Splice_Rec_1266502,Human_Splice_Rec_1266524,Human_Splice_Rec_1266546,Human_Splice_Rec_1266552 Human_miRNA_ID_1193414 57224 RMVar_ID_57224 Human_SNP_ID_470572277 m1A Human chr11 + 67438776 67438776 67438776 GAGGAGCCCGGGGCCATGGCGGGCCGGCTGTCAGACAACACGTTGCGCCGGCTGATCTTCAGGTC GAGGAGCCCGGGGCCATGGCGGGCCGGCTGTCCGACAACACGTTGCGCCGGCTGATCTTCAGGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67438725..67438826 26863196 MeRIP-seq:(Medium) rs34026289 Functional Loss SNV dbSNP153 33..33 33 - - - 57225 RMVar_ID_57225 Human_SNP_ID_470572278 m1A Human chr11 + 67438776 67438776 67438776 GAGGAGCCCGGGGCCATGGCGGGCCGGCTGTCAGACAACACGTTGCGCCGGCTGATCTTCAGGTC GAGGAGCCCGGGGCCATGGCGGGCCGGCTGTCGGACAACACGTTGCGCCGGCTGATCTTCAGGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67438725..67438826 26863196 MeRIP-seq:(Medium) rs34026289 Functional Loss SNV dbSNP153 33..33 33 - - - 57226 RMVar_ID_57226 Human_SNP_ID_470572780 m1A Human chr11 - 67440178 67440178 67440178 CTTCCTGAACACGTTCACCAGCAAGGAGCCGCAGCGGGGTATGGGCAGCATGCCCAAGCGGGGCC CTTCCTGAACACGTTCACCAGCAAGGAGCCGCGGCGGGGTATGGGCAGCATGCCCAAGCGGGGCC T C CORO1B Ensembl:ENSG00000172725 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67440092..67440318 26863196 MeRIP-seq:(Medium) rs1369841355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9321653,Human_RBP_ID_22433141,Human_RBP_ID_22569651 Human_Splice_Rec_1266476,Human_Splice_Rec_1266477,Human_Splice_Rec_1266496,Human_Splice_Rec_1266497,Human_Splice_Rec_1266518,Human_Splice_Rec_1266519,Human_Splice_Rec_1266540,Human_Splice_Rec_1266541,Human_Splice_Rec_1266547,Human_Splice_Rec_1266554 RMVar_hsa_circ_42228 57227 RMVar_ID_57227 Human_SNP_ID_470572798 m1A Human chr11 + 67440222 67440222 67440222 CTGGTGAACGTGTTCAGGAAGTGGATGTAGGGAGGCTCCTCTGTGATCTCAAAGTACCGGATGCT CTGGTGAACGTGTTCAGGAAGTGGATGTAGGGCGGCTCCTCTGTGATCTCAAAGTACCGGATGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67440001..67440472 26863196 MeRIP-seq:(Medium) rs754173763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11687582 57228 RMVar_ID_57228 Human_SNP_ID_470572799 m1A Human chr11 + 67440222 67440222 67440222 CTGGTGAACGTGTTCAGGAAGTGGATGTAGGGAGGCTCCTCTGTGATCTCAAAGTACCGGATGCT CTGGTGAACGTGTTCAGGAAGTGGATGTAGGGTGGCTCCTCTGTGATCTCAAAGTACCGGATGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67440001..67440472 26863196 MeRIP-seq:(Medium) rs754173763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11687582 57229 RMVar_ID_57229 Human_SNP_ID_470573166 m1A Human chr11 + 67441210 67441210 67441210 ACACCTTGCCATCTGCCAGGAAGATGGCCCGCATGGGCCGGGCCCCCTCATGAGCCTTCTCCCGC ACACCTTGCCATCTGCCAGGAAGATGGCCCGCGTGGGCCGGGCCCCCTCATGAGCCTTCTCCCGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67441170..67441375 26863196 MeRIP-seq:(Medium) rs758796112 Functional Loss SNV dbSNP153 33..33 33 - - - 57230 RMVar_ID_57230 Human_SNP_ID_470573981 m1A Human chr11 + 67443368 67443368 67443368 CAGCCCGGCCCCTGCAGCCCCGCCCAGCCCCCAGCCCGCGCCCCTAGCCCCGGCCCTGCCGCGCT CAGCCCGGCCCCTGCAGCCCCGCCCAGCCCCCGGCCCGCGCCCCTAGCCCCGGCCCTGCCGCGCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67443358..67443475 26863410 MeRIP-seq:(Medium) rs1335561019 Functional Loss SNV dbSNP153 33..33 33 - - - 57231 RMVar_ID_57231 Human_SNP_ID_470578613 m1A Human chr11 - 67458688 67458688 67458688 GCAGCCTGGGTCTGGCTGGTGTCTGGGGCCGCAGGGGCAACAGATATTCCCTCCTGGAGCCTCAG GCAGCCTGGGTCTGGCTGGTGTCTGGGGCCGCCGGGGCAACAGATATTCCCTCCTGGAGCCTCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67458680..67458789 26863196 MeRIP-seq:(Medium) rs1008239273 Functional Loss SNV dbSNP153 33..33 33 - - - 57232 RMVar_ID_57232 Human_SNP_ID_470580547 m1A Human chr11 - 67465102 67465102 67465102 CTGCCCCCACCCCCGCGGCTCCGTCTGTGTGCAGTGCTGATCCTGGTCGGCGTGGGACTGGAGGC CTGCCCCCACCCCCGCGGCTCCGTCTGTGTGCGGTGCTGATCCTGGTCGGCGTGGGACTGGAGGC T C TMEM134 Ensembl:ENSG00000172663 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67464860..67465111 26863196 MeRIP-seq:(Medium) rs200668561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402047,Human_RBP_ID_18974395,Human_RBP_ID_19050078 Human_Splice_Rec_1266633,Human_Splice_Rec_1266645,Human_Splice_Rec_1266655,Human_Splice_Rec_1266667,Human_Splice_Rec_1266675,Human_Splice_Rec_1266695 RMVar_hsa_circ_98711,RMVar_hsa_circ_151066 57233 RMVar_ID_57233 Human_SNP_ID_470581711 m1A Human chr11 - 67469083 67469083 67469083 GTCCAGCGGGGTCGCGCGCTTTGGGCCGCTGCACTTCGAGCGTCGGGCCCGGTTCGAGGTGGCTG GTCCAGCGGGGTCGCGCGCTTTGGGCCGCTGCTCTTCGAGCGTCGGGCCCGGTTCGAGGTGGCTG T A TMEM134 Ensembl:ENSG00000172663 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67468003..67469172 32194978 MeRIP-seq:(Medium) rs1337728218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185184 Human_Splice_Rec_1266625,Human_Splice_Rec_1266637,Human_Splice_Rec_1266657,Human_Splice_Rec_1266679,Human_Splice_Rec_1266699,Human_Splice_Rec_1266705,Human_Splice_Rec_1266711,Human_Splice_Rec_1266719,Human_Splice_Rec_1266725,Human_Splice_Rec_1266729,Human_Splice_Rec_1266733,Human_Splice_Rec_1266737 57234 RMVar_ID_57234 Human_SNP_ID_470581792 m1A Human chr11 - 67469216 67469205 67469216 GCTGGGTGTGTGGGCGCAGATGGCGGCGGCGCACGGCGCCTGAGCGGGCCGGGGCCATGAGCGCC GCTGGGTGTGTGGGCGCAGATGGCGGCGGCGC___________GCGGGCCGGGGCCATGAGCGCC CTCAGGCGCCGT C TMEM134 Ensembl:ENSG00000172663 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:67469083..67469250;chr11:67469094..67469236 26863196 MeRIP-seq:(Medium) rs1189764814 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_4175417 57235 RMVar_ID_57235 Human_SNP_ID_470581802 m1A Human chr11 - 67469216 67469216 67469216 GCTGGGTGTGTGGGCGCAGATGGCGGCGGCGCACGGCGCCTGAGCGGGCCGGGGCCATGAGCGCC GCTGGGTGTGTGGGCGCAGATGGCGGCGGCGCGCGGCGCCTGAGCGGGCCGGGGCCATGAGCGCC T C TMEM134 Ensembl:ENSG00000172663 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:67469083..67469250;chr11:67469094..67469236 26863196 MeRIP-seq:(Medium) rs891444386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4175417 57236 RMVar_ID_57236 Human_SNP_ID_470585634 m1A Human chr11 - 67483196 67483196 67483196 CTCCTCGGCCTTCCTGTATCACACGTTTTTGGATCCCGTCCTCCCGGAGTCTTGCGATGATATCC CTCCTCGGCCTTCCTGTATCACACGTTTTTGGTTCCCGTCCTCCCGGAGTCTTGCGATGATATCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67483026..67487175 26863196 MeRIP-seq:(Medium) rs376913545 Functional Loss SNV dbSNP153 33..33 33 - - - 57237 RMVar_ID_57237 Human_SNP_ID_470585636 m1A Human chr11 + 67483199 67483199 67483199 TATCATCGCAAGACTCCGGGAGGACGGGATCCAAAAACGTGTGATACAGGAAGGCCGAGGAGAGC TATCATCGCAAGACTCCGGGAGGACGGGATCCCAAAACGTGTGATACAGGAAGGCCGAGGAGAGC A C AIP Ensembl:ENSG00000110711 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:67483148..67483273 26863196 MeRIP-seq:(Medium) rs1317189253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808337,Human_RBP_ID_988197,Human_RBP_ID_5490192,Human_RBP_ID_8357122,Human_RBP_ID_17800061,Human_RBP_ID_21883085,Human_RBP_ID_23517148 Human_Splice_Rec_1266739,Human_Splice_Rec_1266749,Human_Splice_Rec_1266757 RMVar_hsa_circ_103564,RMVar_hsa_circ_151067 57238 RMVar_ID_57238 Human_SNP_ID_470585660 m1A Human chr11 + 67483245 67483244 67483246 CAGGAAGGCCGAGGAGAGCTCCCGGACTTTCAAGATGGGACCAAGGTTCGTGTCTACCCTACCCT CAGGAAGGCCGAGGAGAGCTCCCGGACTTTCA__ATGGGACCAAGGTTCGTGTCTACCCTACCCT AAG A AIP Ensembl:ENSG00000110711 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67483151..67487037 26863410 MeRIP-seq:(Medium) rs267606584 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26318888,Human_RBP_ID_26804986 Human_Splice_Rec_1266739,Human_Splice_Rec_1266749,Human_Splice_Rec_1266757 Human_miRNA_ID_2034220,Human_miRNA_ID_2035524 RMVar_hsa_circ_103564,RMVar_hsa_circ_151067 57239 RMVar_ID_57239 Human_SNP_ID_470585661 m1A Human chr11 + 67483245 67483245 67483245 CAGGAAGGCCGAGGAGAGCTCCCGGACTTTCAAGATGGGACCAAGGTTCGTGTCTACCCTACCCT CAGGAAGGCCGAGGAGAGCTCCCGGACTTTCAGGATGGGACCAAGGTTCGTGTCTACCCTACCCT A G AIP Ensembl:ENSG00000110711 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67483151..67487037 26863410 MeRIP-seq:(Medium) rs763596431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26318888,Human_RBP_ID_26804986 Human_Splice_Rec_1266739,Human_Splice_Rec_1266749,Human_Splice_Rec_1266757 Human_miRNA_ID_2034220,Human_miRNA_ID_2035524 RMVar_hsa_circ_103564,RMVar_hsa_circ_151067 57240 RMVar_ID_57240 Human_SNP_ID_470587498 m1A Human chr11 + 67490177 67490177 67490177 GGGGCATGTGAAGGAGGCTGCTGCCAAGTACTACGATGCCATTGCCTGCCTCAAGAACCTGCAGA GGGGCATGTGAAGGAGGCTGCTGCCAAGTACTGCGATGCCATTGCCTGCCTCAAGAACCTGCAGA A G AIP Ensembl:ENSG00000110711 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:67490126..67490225 32194978 MeRIP-seq:(Medium) rs746245790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402062,Human_RBP_ID_988201,Human_RBP_ID_1459796,Human_RBP_ID_18974399 Human_Splice_Rec_1266745,Human_Splice_Rec_1266753,Human_Splice_Rec_1266763 RMVar_hsa_circ_84347,RMVar_hsa_circ_103564,RMVar_hsa_circ_114401,RMVar_hsa_circ_151067,RMVar_hsa_circ_151068,RMVar_hsa_circ_151069 57241 RMVar_ID_57241 Human_SNP_ID_470587822 m1A Human chr11 + 67490959 67490959 67490959 GGAGGCACGGATCCGGCAGAAGGACGAAGAGGACAAAGCCCGGTTCCGGGGGATCTTCTCCCATT GGAGGCACGGATCCGGCAGAAGGACGAAGAGGGCAAAGCCCGGTTCCGGGGGATCTTCTCCCATT A G AIP Ensembl:ENSG00000110711 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67490776..67491075 32194978 MeRIP-seq:(Medium) rs1282118820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17649211 RMVar_hsa_circ_84347,RMVar_hsa_circ_103564,RMVar_hsa_circ_114401,RMVar_hsa_circ_151067,RMVar_hsa_circ_151068,RMVar_hsa_circ_151069 57242 RMVar_ID_57242 Human_SNP_ID_470589278 m1A Human chr11 - 67494904 67494904 67494904 ACAGCTGGCGGAATGCGAGGAGCCGTCCATCTACAGCCCGGCCTTCCCCAGGGAGAAGTGGCAGC ACAGCTGGCGGAATGCGAGGAGCCGTCCATCTGCAGCCCGGCCTTCCCCAGGGAGAAGTGGCAGC T C PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:67494845..67495023 26863196 MeRIP-seq:(Medium) rs776886702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4175471 Human_Splice_Rec_1266794,Human_Splice_Rec_1266795,Human_Splice_Rec_1266838,Human_Splice_Rec_1266839,Human_Splice_Rec_1266882,Human_Splice_Rec_1266883,Human_Splice_Rec_1266906,Human_Splice_Rec_1266907,Human_Splice_Rec_1266919,Human_Splice_Rec_1266926,Human_Splice_Rec_1266927 RMVar_hsa_circ_123739,RMVar_hsa_circ_80744,RMVar_hsa_circ_151071,RMVar_hsa_circ_151072 57243 RMVar_ID_57243 Human_SNP_ID_470589578 m1A Human chr11 + 67495593 67495592 67495594 GCTCCTCCAGAAAGAGGCTGGAGTGCGTCTGCAGAGTGTCGGCTGGGGGAAGGAGGGCAAGGTCA GCTCCTCCAGAAAGAGGCTGGAGTGCGTCTGC__AGTGTCGGCTGGGGGAAGGAGGGCAAGGTCA CAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:67495464..67495667 26863196 MeRIP-seq:(Medium) rs763961947 Functional Loss DEL dbSNP153 33..34 33 - - - 57244 RMVar_ID_57244 Human_SNP_ID_470589579 m1A Human chr11 + 67495593 67495593 67495593 GCTCCTCCAGAAAGAGGCTGGAGTGCGTCTGCAGAGTGTCGGCTGGGGGAAGGAGGGCAAGGTCA GCTCCTCCAGAAAGAGGCTGGAGTGCGTCTGCGGAGTGTCGGCTGGGGGAAGGAGGGCAAGGTCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:67495464..67495667 26863196 MeRIP-seq:(Medium) rs546525203 Functional Loss SNV dbSNP153 33..33 33 - - - 57245 RMVar_ID_57245 Human_SNP_ID_470589824 m1A Human chr11 - 67496347 67496347 67496347 CCACAATCTTTCTCTGTCTTCTGGGTACCAGCAGCCCAGATGCGCCCAGCCTGTGAACAGATCTA CCACAATCTTTCTCTGTCTTCTGGGTACCAGCCGCCCAGATGCGCCCAGCCTGTGAACAGATCTA T G PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67495223..67496406 32194978 MeRIP-seq:(Medium) rs866155530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867934,Human_RBP_ID_22641726 Human_Splice_Rec_1266788,Human_Splice_Rec_1266832 RMVar_hsa_circ_123739,RMVar_hsa_circ_80744,RMVar_hsa_circ_151071,RMVar_hsa_circ_151072 57246 RMVar_ID_57246 Human_SNP_ID_470590491 m1A Human chr11 + 67498290 67498290 67498290 CAGCCAGTGGAATGTGGTCTTGGGAGCGAGACAGGCTGTCCCCATCGTGGCTGTAAGGGCTCAGG CAGCCAGTGGAATGTGGTCTTGGGAGCGAGACGGGCTGTCCCCATCGTGGCTGTAAGGGCTCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67498137..67498300 26863196 MeRIP-seq:(Medium) rs768342324 Functional Loss SNV dbSNP153 33..33 33 - - - 57247 RMVar_ID_57247 Human_SNP_ID_470591179 m1A Human chr11 - 67500215 67500215 67500215 GGAAACCGAGCACCGAGGCCCGGTCTGCGGCCAGCAACACTGGCACCCCCGATGGGCCTGAGGCC GGAAACCGAGCACCGAGGCCCGGTCTGCGGCCGGCAACACTGGCACCCCCGATGGGCCTGAGGCC T C PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67500169..67500339 26863196 MeRIP-seq:(Medium) rs1049031165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80744,RMVar_hsa_circ_151072,RMVar_hsa_circ_124441,RMVar_hsa_circ_151075,RMVar_hsa_circ_104213,RMVar_hsa_circ_151077 57248 RMVar_ID_57248 Human_SNP_ID_470591189 m1A Human chr11 - 67500239 67500239 67500239 AGGGGTCCGAGGCCCAGCCCCCCGGGAAACCGAGCACCGAGGCCCGGTCTGCGGCCAGCAACACT AGGGGTCCGAGGCCCAGCCCCCCGGGAAACCGGGCACCGAGGCCCGGTCTGCGGCCAGCAACACT T C PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67500146..67500297 26863410 MeRIP-seq:(Medium) rs1040122628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80744,RMVar_hsa_circ_151072,RMVar_hsa_circ_124441,RMVar_hsa_circ_151075,RMVar_hsa_circ_104213,RMVar_hsa_circ_151077 57249 RMVar_ID_57249 Human_SNP_ID_470591926 m1A Human chr11 - 67502717 67502717 67502717 GCTCCCTGTCCTGCTCTCCCTTGGGCCACAGAAAAAGAGCCGGGAGGAGTCTAGTGGTGAGGGCA GCTCCCTGTCCTGCTCTCCCTTGGGCCACAGAGAAAGAGCCGGGAGGAGTCTAGTGGTGAGGGCA T C PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67502574..67502764 26863196 MeRIP-seq:(Medium) rs745905500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22641730 Human_Splice_Rec_1266766,Human_Splice_Rec_1266810,Human_Splice_Rec_1266854,Human_Splice_Rec_1266940,Human_Splice_Rec_1266948,Human_Splice_Rec_1266956,Human_Splice_Rec_1266962,Human_Splice_Rec_1266968 RMVar_hsa_circ_594,RMVar_hsa_circ_80744,RMVar_hsa_circ_151072 57250 RMVar_ID_57250 Human_SNP_ID_470592152 m1A Human chr11 + 67503715 67503714 67503715 CCCTCCCATCCTTGCTGCCCTGTCCCTGCTCCAGGTTTGACACCTGGTCCTCACCACATCTCCCT CCCTCCCATCCTTGCTGCCCTGTCCCTGCTCC_GGTTTGACACCTGGTCCTCACCACATCTCCCT CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67503711..67503846 26863196 MeRIP-seq:(Medium) rs1210215431 Functional Loss DEL dbSNP153 33..33 33 - - - 57251 RMVar_ID_57251 Human_SNP_ID_470592277 m1A Human chr11 - 67504183 67504183 67504183 CGGAGGCCGCGCGCGGCCCGCCGAGCGCCTTCAGGATGCTCATCAAGGAATACCACATTCTGCTG CGGAGGCCGCGCGCGGCCCGCCGAGCGCCTTCGGGATGCTCATCAAGGAATACCACATTCTGCTG T C PITPNM1 Ensembl:ENSG00000110697 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67503953..67504382 26863196 MeRIP-seq:(Medium) rs1319537822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23207378 Human_Splice_Rec_1266765,Human_Splice_Rec_1266808,Human_Splice_Rec_1266809,Human_Splice_Rec_1266852,Human_Splice_Rec_1266853,Human_Splice_Rec_1266939,Human_Splice_Rec_1266946,Human_Splice_Rec_1266947,Human_Splice_Rec_1266954,Human_Splice_Rec_1266955,Human_Splice_Rec_1266966,Human_Splice_Rec_1266967,Human_Splice_Rec_1266970,Human_Splice_Rec_1266971 RMVar_hsa_circ_80744,RMVar_hsa_circ_151072 57252 RMVar_ID_57252 Human_SNP_ID_470592598 m1A Human chr11 + 67505213 67505213 67505213 GGCTCACCTCTAGCTTGAGGCGGGCGCCCCTCACCCAGCCCGGGCAGGGCCGGCCGGCCCGTGGG GGCTCACCTCTAGCTTGAGGCGGGCGCCCCTCCCCCAGCCCGGGCAGGGCCGGCCGGCCCGTGGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:67505159..67505333 26863196 MeRIP-seq:(Medium) rs917784859 Functional Loss SNV dbSNP153 33..33 33 - - - 57253 RMVar_ID_57253 Human_SNP_ID_470592985 m1A Human chr11 - 67506672 67506672 67506672 GCCCACCGGAACTTTTGTGGCCCCTACCGCTCAGCCCTTCCCAGCACTTCTCCCACTTTGTCCCG GCCCACCGGAACTTTTGTGGCCCCTACCGCTCGGCCCTTCCCAGCACTTCTCCCACTTTGTCCCG T C CDK2AP2 Ensembl:ENSG00000167797 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67506576..67507025 26863196 MeRIP-seq:(Medium) rs1358510222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402083,Human_RBP_ID_5110548,Human_RBP_ID_17074009,Human_RBP_ID_17350270,Human_RBP_ID_17649212,Human_RBP_ID_18932659 Human_miRNA_ID_1355778,Human_miRNA_ID_2315963,Human_miRNA_ID_2319117,Human_miRNA_ID_2322277,Human_miRNA_ID_2325445,Human_miRNA_ID_2519821,Human_miRNA_ID_2522986,Human_miRNA_ID_2774806,Human_miRNA_ID_2822181,Human_miRNA_ID_2828311,Human_miRNA_ID_2831468,Human_miRNA_ID_2835587,Human_miRNA_ID_2840943 RMVar_hsa_circ_113586,RMVar_hsa_circ_151078 57254 RMVar_ID_57254 Human_SNP_ID_470612531 m1A Human chr11 - 67584129 67584129 67584129 GGGAAATAGACCACGGTGTAGGGCGGCACTGCAGCGAACAAAGAAAAGTTTGCTGGAGCCCGGGG GGGAAATAGACCACGGTGTAGGGCGGCACTGCGGCGAACAAAGAAAAGTTTGCTGGAGCCCGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:67584126..67584175 26863196 MeRIP-seq:(Medium) rs756699982 Functional Loss SNV dbSNP153 33..33 33 - - - 57255 RMVar_ID_57255 Human_SNP_ID_470612647 m1A Human chr11 - 67584455 67584455 67584455 GCATGCGCAGGGCCGCGCAGCGGCCTGCGGGGAGGGAGAAGTACGAGATGTGGGGACCGGGCCGA GCATGCGCAGGGCCGCGCAGCGGCCTGCGGGGTGGGAGAAGTACGAGATGTGGGGACCGGGCCGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:67584451..67584475 26863196 MeRIP-seq:(Medium) rs1459961868 Functional Loss SNV dbSNP153 33..33 33 - - - 57256 RMVar_ID_57256 Human_SNP_ID_470612793 m1A Human chr11 - 67584774 67584774 67584774 ATGCCTGCCCTGGACTTGGAGGTTCAAGACTCACCAAGGGTGCGGCCCAGGTGACGCAGGATGGT ATGCCTGCCCTGGACTTGGAGGTTCAAGACTCCCCAAGGGTGCGGCCCAGGTGACGCAGGATGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67584443..67584816 26863196 MeRIP-seq:(Medium) rs80247966 Functional Loss SNV dbSNP153 33..33 33 - - - 57257 RMVar_ID_57257 Human_SNP_ID_470612936 m1A Human chr11 - 67585209 67585207 67585209 ATAGTTGGTGTAGATGAGGGAGATGTATTTGCAGCGGAGGTCCTCCACGCCGTCATTCACCATGT ATAGTTGGTGTAGATGAGGGAGATGTATTTGC__CGGAGGTCCTCCACGCCGTCATTCACCATGT GCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67585103..67585284 26863196 MeRIP-seq:(Medium) rs1469309644 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_151088 57258 RMVar_ID_57258 Human_SNP_ID_470613187 m1A Human chr11 - 67586029 67586029 67586029 AGCCCCTGAGACACCCCCGTCTGCCCCAGGCCAGACACCAGAGTCCCAGATTCTCCTCTGCTTGC AGCCCCTGAGACACCCCCGTCTGCCCCAGGCCGGACACCAGAGTCCCAGATTCTCCTCTGCTTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67586026..67586127 26863196 MeRIP-seq:(Medium) rs551558365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151088 57259 RMVar_ID_57259 Human_SNP_ID_470613243 m1A Human chr11 - 67586155 67586155 67586155 GCCTCCCTGGTTCTGGGACAGCAGGGTCTCAAAAGGCTTCAGTTGCCCGGGCAGTGCCTTCACAT GCCTCCCTGGTTCTGGGACAGCAGGGTCTCAACAGGCTTCAGTTGCCCGGGCAGTGCCTTCACAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:67586042..67586243;chr11:67585961..67586159 26863196 MeRIP-seq:(Medium) rs370396702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151088 57260 RMVar_ID_57260 Human_SNP_ID_470613258 m1A Human chr11 + 67586189 67586189 67586189 TGAGACCCTGCTGTCCCAGAACCAGGGAGGCAAGACCTTCATTGTGGGAGACCAGGTGAGCATCT TGAGACCCTGCTGTCCCAGAACCAGGGAGGCAGGACCTTCATTGTGGGAGACCAGGTGAGCATCT A G GSTP1 Ensembl:ENSG00000084207 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67585159..67586267 32194978 MeRIP-seq:(Medium) rs553211668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402108,Human_RBP_ID_749004,Human_RBP_ID_17648461,Human_RBP_ID_18188338,Human_RBP_ID_22433153,Human_RBP_ID_26805012 Human_Splice_Rec_1267060,Human_Splice_Rec_1267061,Human_Splice_Rec_1267066,Human_Splice_Rec_1267074,Human_Splice_Rec_1267075,Human_Splice_Rec_1267086,Human_Splice_Rec_1267087,Human_Splice_Rec_1267090,Human_Splice_Rec_1267091,Human_Splice_Rec_1267093 Human_miRNA_ID_2611319,Human_miRNA_ID_2727840,Human_miRNA_ID_2868108 RMVar_hsa_circ_83436,RMVar_hsa_circ_109001,RMVar_hsa_circ_151079,RMVar_hsa_circ_93515,RMVar_hsa_circ_151080,RMVar_hsa_circ_92182,RMVar_hsa_circ_114794,RMVar_hsa_circ_151085,RMVar_hsa_circ_92949,RMVar_hsa_circ_151086,RMVar_hsa_circ_151087,RMVar_hsa_circ_151089 57261 RMVar_ID_57261 Human_SNP_ID_470613367 m1A Human chr11 - 67586471 67586471 67586471 GGGCACTGAGGCGCCCCACATATGCTGAGAGCAGGGGGAACGCATCCAGGCAGCCAGGGGCTAGG GGGCACTGAGGCGCCCCACATATGCTGAGAGCGGGGGGAACGCATCCAGGCAGCCAGGGGCTAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:67586451..67586475 26863196 MeRIP-seq:(Medium) rs766852045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151088 57262 RMVar_ID_57262 Human_SNP_ID_470613380 m1A Human chr11 - 67586499 67586499 67586499 GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCACTGAGGCGCCCCACATATGCTGAGAGCAGGGG GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCGCTGAGGCGCCCCACATATGCTGAGAGCAGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67586456..67586582 26863196 MeRIP-seq:(Medium) rs4891 Functional Loss SNV dbSNP153,EGP,HGVD 33..33 33 - - - GWAS_ID_6712,GWAS_ID_6713,GWAS_ID_6714,GWAS_ID_6715,GWAS_ID_6716,GWAS_ID_6717,GWAS_ID_6718,GWAS_ID_6719 RMVar_hsa_circ_151088 57263 RMVar_ID_57263 Human_SNP_ID_470613407 m1A Human chr11 + 67586554 67586554 67586554 TCCTGGCCTCCCCTGAGTACGTGAACCTCCCCATCAATGGCAACGGGAAACAGTGAGGGTTGGGG TCCTGGCCTCCCCTGAGTACGTGAACCTCCCCGTCAATGGCAACGGGAAACAGTGAGGGTTGGGG A G GSTP1 Ensembl:ENSG00000084207 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67586350..67586601 26863196 MeRIP-seq:(Medium) rs762582956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402118,Human_RBP_ID_17648814,Human_RBP_ID_18188586,Human_RBP_ID_22435517,Human_RBP_ID_22792052,Human_RBP_ID_26803910 Human_miRNA_ID_2367272,Human_miRNA_ID_3015069,Human_miRNA_ID_3101229 RMVar_hsa_circ_83436,RMVar_hsa_circ_109001,RMVar_hsa_circ_151079,RMVar_hsa_circ_93515,RMVar_hsa_circ_151080,RMVar_hsa_circ_92182,RMVar_hsa_circ_114794,RMVar_hsa_circ_151085,RMVar_hsa_circ_92949,RMVar_hsa_circ_151086,RMVar_hsa_circ_151087,RMVar_hsa_circ_97538,RMVar_hsa_circ_151089,RMVar_hsa_circ_151090 57264 RMVar_ID_57264 Human_SNP_ID_470613409 m1A Human chr11 + 67586563 67586563 67586563 CCCCTGAGTACGTGAACCTCCCCATCAATGGCAACGGGAAACAGTGAGGGTTGGGGGGACTCTGA CCCCTGAGTACGTGAACCTCCCCATCAATGGCCACGGGAAACAGTGAGGGTTGGGGGGACTCTGA A C GSTP1 Ensembl:ENSG00000084207 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67586512..67586650 32194978 MeRIP-seq:(Medium) rs1316398882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402118,Human_RBP_ID_8357150,Human_RBP_ID_17648814,Human_RBP_ID_18188586,Human_RBP_ID_22435517,Human_RBP_ID_22792052,Human_RBP_ID_26803910 Human_miRNA_ID_2647980,Human_miRNA_ID_2670577,Human_miRNA_ID_3101229 RMVar_hsa_circ_83436,RMVar_hsa_circ_109001,RMVar_hsa_circ_151079,RMVar_hsa_circ_93515,RMVar_hsa_circ_151080,RMVar_hsa_circ_92182,RMVar_hsa_circ_114794,RMVar_hsa_circ_151085,RMVar_hsa_circ_92949,RMVar_hsa_circ_151086,RMVar_hsa_circ_151087,RMVar_hsa_circ_97538,RMVar_hsa_circ_151089,RMVar_hsa_circ_151090 57265 RMVar_ID_57265 Human_SNP_ID_470613414 m1A Human chr11 - 67586581 67586581 67586581 GCAAACTCTGCCTCCCGCTCAGAGTCCCCCCAACCCTCACTGTTTCCCGTTGCCATTGATGGGGA GCAAACTCTGCCTCCCGCTCAGAGTCCCCCCAGCCCTCACTGTTTCCCGTTGCCATTGATGGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67586355..67586602 26863196 MeRIP-seq:(Medium) rs756966448 Functional Loss SNV dbSNP153 33..33 33 - - - 57266 RMVar_ID_57266 Human_SNP_ID_470618542 m1A Human chr11 - 67607051 67607051 67607051 GCCTCACCGTGTCGCCGCTGAAACGCACAGATACCCGCGCGGGAAGCGACCAGCCGAGCAGCCGC GCCTCACCGTGTCGCCGCTGAAACGCACAGATCCCCGCGCGGGAAGCGACCAGCCGAGCAGCCGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:67607001..67607100;chr11:67606951..67607075 32194978 MeRIP-seq:(Medium) rs1009992400 Functional Loss SNV dbSNP153 33..33 33 - - - 57267 RMVar_ID_57267 Human_SNP_ID_470619318 m1A Human chr11 - 67609556 67609556 67609556 AGGCAGCGCGGGCGCCCATGGCCCGGCCCCCCACCAGGCAGCCTTCCAGCAGCTTGTGAGGATCA AGGCAGCGCGGGCGCCCATGGCCCGGCCCCCCCCCAGGCAGCCTTCCAGCAGCTTGTGAGGATCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67609406..67609675 26863196 MeRIP-seq:(Medium) rs759396220 Functional Loss SNV dbSNP153 33..33 33 - - - 57268 RMVar_ID_57268 Human_SNP_ID_470619766 m1A Human chr11 + 67611051 67611051 67611051 TGGCCAACGTGGAGACAGTGGCAGTGTCCCCCACAATCTGCCGCCGTGGAGGTACCTGGTTTGCT TGGCCAACGTGGAGACAGTGGCAGTGTCCCCCGCAATCTGCCGCCGTGGAGGTACCTGGTTTGCT A G NDUFV1 Ensembl:ENSG00000167792 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67611001..67611125 32194978 MeRIP-seq:(Medium) rs756156992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402141,Human_RBP_ID_4175587,Human_RBP_ID_22895443 Human_Splice_Rec_1267114,Human_Splice_Rec_1267130,Human_Splice_Rec_1267162,Human_Splice_Rec_1267180,Human_Splice_Rec_1267218,Human_Splice_Rec_1267310,Human_Splice_Rec_1267316 RMVar_hsa_circ_63940,RMVar_hsa_circ_314785,RMVar_hsa_circ_71710,RMVar_hsa_circ_320028 57269 RMVar_ID_57269 Human_SNP_ID_470619803 m1A Human chr11 + 67611142 67611142 67611142 CACCAAACTATTCAACATCTCTGGCCATGTCAACCACCCTTGCACTGTGGAGGAGGAGATGTCTG CACCAAACTATTCAACATCTCTGGCCATGTCAGCCACCCTTGCACTGTGGAGGAGGAGATGTCTG A G NDUFV1 Ensembl:ENSG00000167792 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67610971..67611237 26863196 MeRIP-seq:(Medium) rs754023854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3378774,Human_RBP_ID_3939578,Human_RBP_ID_8357166,Human_RBP_ID_18611802,Human_RBP_ID_22433161 Human_Splice_Rec_1267115,Human_Splice_Rec_1267131,Human_Splice_Rec_1267163,Human_Splice_Rec_1267181,Human_Splice_Rec_1267219,Human_Splice_Rec_1267297,Human_Splice_Rec_1267311,Human_Splice_Rec_1267317,Human_Splice_Rec_1267325 RMVar_hsa_circ_63940,RMVar_hsa_circ_314785,RMVar_hsa_circ_71710,RMVar_hsa_circ_320028 57270 RMVar_ID_57270 Human_SNP_ID_470619806 m1A Human chr11 - 67611150 67611150 67611150 CAAGGGCACAGACATCTCCTCCTCCACAGTGCAAGGGTGGTTGACATGGCCAGAGATGTTGAATA CAAGGGCACAGACATCTCCTCCTCCACAGTGCGAGGGTGGTTGACATGGCCAGAGATGTTGAATA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67611101..67611200 32194978 MeRIP-seq:(Medium) rs1160694147 Functional Loss SNV dbSNP153 33..33 33 - - - 57271 RMVar_ID_57271 Human_SNP_ID_470619925 m1A Human chr11 - 67611439 67611439 67611439 GGATCAGTGGGGTAGACGAGCCGCCAGGGATCACAGCAAGGAGGTTGTCCCAGCCGCCCGTGACA GGATCAGTGGGGTAGACGAGCCGCCAGGGATCGCAGCAAGGAGGTTGTCCCAGCCGCCCGTGACA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67611401..67611450 32194978 MeRIP-seq:(Medium) rs1555025756 Functional Loss SNV dbSNP153 33..33 33 - - - 57272 RMVar_ID_57272 Human_SNP_ID_470620242 m1A Human chr11 + 67612180 67612180 67612180 ACGTTTCGTGAGGGGGGATGCCCGGCCGGCCGAGATCGACTCCCTGTGGGAGATCAGCAAGCAGA ACGTTTCGTGAGGGGGGATGCCCGGCCGGCCGCGATCGACTCCCTGTGGGAGATCAGCAAGCAGA A C NDUFV1 Ensembl:ENSG00000167792 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:67612098..67612211;chr11:67612104..67612202 26863196 MeRIP-seq:(Medium) rs760250432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226914,Human_RBP_ID_402153,Human_RBP_ID_871782,Human_RBP_ID_3940962,Human_RBP_ID_5110551,Human_RBP_ID_5138700,Human_RBP_ID_5314339,Human_RBP_ID_17648815,Human_RBP_ID_17804688,Human_RBP_ID_18159295,Human_RBP_ID_18972402,Human_RBP_ID_22434678,Human_RBP_ID_22491698,Human_RBP_ID_23517213,Human_RBP_ID_26318890 Human_Splice_Rec_1267120,Human_Splice_Rec_1267121,Human_Splice_Rec_1267136,Human_Splice_Rec_1267137,Human_Splice_Rec_1267168,Human_Splice_Rec_1267169,Human_Splice_Rec_1267186,Human_Splice_Rec_1267187,Human_Splice_Rec_1267224,Human_Splice_Rec_1267225,Human_Splice_Rec_1267302,Human_Splice_Rec_1267303,Human_Splice_Rec_1267322,Human_Splice_Rec_1267323,Human_Splice_Rec_1267328,Human_Splice_Rec_1267329,Human_Splice_Rec_1267334,Human_Splice_Rec_1267336,Human_Splice_Rec_1267337,Human_Splice_Rec_1267339 Human_miRNA_ID_340089,Human_miRNA_ID_1692490,Human_miRNA_ID_2868109 RMVar_hsa_circ_151093,RMVar_hsa_circ_114392 57273 RMVar_ID_57273 Human_SNP_ID_470625162 m1A Human chr11 + 67629808 67629808 67629808 CCGGGACCCCACGCACTGAGCAGAGCGGCACGAGCACCGCGGCCGACGCGGGCCGCGCGCGGAGC CCGGGACCCCACGCACTGAGCAGAGCGGCACGCGCACCGCGGCCGACGCGGGCCGCGCGCGGAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67629769..67629860 26863196 MeRIP-seq:(Medium) rs1324383830 Functional Loss SNV dbSNP153 33..33 33 - - - 57274 RMVar_ID_57274 Human_SNP_ID_470625172 m1A Human chr11 + 67629821 67629821 67629821 CACTGAGCAGAGCGGCACGAGCACCGCGGCCGACGCGGGCCGCGCGCGGAGCCGGGCCGTGGCCC CACTGAGCAGAGCGGCACGAGCACCGCGGCCGCCGCGGGCCGCGCGCGGAGCCGGGCCGTGGCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67629783..67629866 26863196 MeRIP-seq:(Medium) rs368421441 Functional Loss SNV dbSNP153 33..33 33 - - - 57275 RMVar_ID_57275 Human_SNP_ID_470641151 m1A Human chr11 - 67682754 67682754 67682754 TGCAGCATCCAGTTCATCTTAAGAATGTCAACAATTAGTCATGCAATAAATGTTCTGGTTTTAAA TGCAGCATCCAGTTCATCTTAAGAATGTCAACGATTAGTCATGCAATAAATGTTCTGGTTTTAAA T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879110440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26410684 57276 RMVar_ID_57276 Human_SNP_ID_470641228 m1A Human chr11 - 67683044 67683044 67683044 CTCGGCCGCAGAAGCGAGATGACGAAGGGAGCATCATCGTTTGGAAAGCATCGCAATAAGACACA CTCGGCCGCAGAAGCGAGATGACGAAGGGAGCGTCATCGTTTGGAAAGCATCGCAATAAGACACA T C RPL37P2 Ensembl:ENSG00000239559 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs999102448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22893526,Human_RBP_ID_26410685 57277 RMVar_ID_57277 Human_SNP_ID_470681007 m1A Human chr11 + 67805267 67805267 67805267 GCAGTGCACGCGCCGCCAGGAAGCGGCGCTCCAAACTCTGCAGCAAGAGTTCGGTCCCCGCGTTC GCAGTGCACGCGCCGCCAGGAAGCGGCGCTCCTAACTCTGCAGCAAGAGTTCGGTCCCCGCGTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67805197..67805267 26863196 MeRIP-seq:(Medium) rs763587178 Functional Loss SNV dbSNP153 33..33 33 - - - 57278 RMVar_ID_57278 Human_SNP_ID_470740543 m1A Human chr11 - 67991567 67991567 67991567 CGGCCCTGCCCGTACGAACAGGCGCAGGGGGGAGACGGGCCGGAGGAGCAGTGAGGGGCCGCCTG CGGCCCTGCCCGTACGAACAGGCGCAGGGGGGGGACGGGCCGGAGGAGCAGTGAGGGGCCGCCTG T C UNC93B1 Ensembl:ENSG00000110057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67991546..67991648 26863196 MeRIP-seq:(Medium) rs4014578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84573,RMVar_hsa_circ_151094 57279 RMVar_ID_57279 Human_SNP_ID_470740544 m1A Human chr11 - 67991567 67991567 67991567 CGGCCCTGCCCGTACGAACAGGCGCAGGGGGGAGACGGGCCGGAGGAGCAGTGAGGGGCCGCCTG CGGCCCTGCCCGTACGAACAGGCGCAGGGGGGCGACGGGCCGGAGGAGCAGTGAGGGGCCGCCTG T G UNC93B1 Ensembl:ENSG00000110057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67991546..67991648 26863196 MeRIP-seq:(Medium) rs4014578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84573,RMVar_hsa_circ_151094 57280 RMVar_ID_57280 Human_SNP_ID_470740570 m1A Human chr11 + 67991607 67991607 67991607 GCGCCTGTTCGTACGGGCAGGGCCGGCGGCCGAGTCCAGCGGGCTCGGGGCCAGGCCTGGGCCCT GCGCCTGTTCGTACGGGCAGGGCCGGCGGCCGTGTCCAGCGGGCTCGGGGCCAGGCCTGGGCCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:67991556..67991631 26863196 MeRIP-seq:(Medium) rs1402199169 Functional Loss SNV dbSNP153 33..33 33 - - - 57281 RMVar_ID_57281 Human_SNP_ID_470742506 m1A Human chr11 - 67997528 67997528 67997528 GGGGCAGGCCGTAGGCCTGGGAGCGCGATCTGAGTTGGGGAGCTAGGGCCGAGTGCTGCAGAGCG GGGGCAGGCCGTAGGCCTGGGAGCGCGATCTGTGTTGGGGAGCTAGGGCCGAGTGCTGCAGAGCG T A UNC93B1 Ensembl:ENSG00000110057 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67997351..67997660 26863196 MeRIP-seq:(Medium) rs551864802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344147,Human_RBP_ID_19050091 RMVar_hsa_circ_47342,RMVar_hsa_circ_305188,RMVar_hsa_circ_87256,RMVar_hsa_circ_151095 57282 RMVar_ID_57282 Human_SNP_ID_470744418 m1A Human chr11 - 68003901 68003901 68003901 GGAGTGCGAGGCGCGGGCGTCCCCTGTGGGCCAGGGTCCCCCCGGCGGGGGCGGGGCGGGCCGGG GGAGTGCGAGGCGCGGGCGTCCCCTGTGGGCCCGGGTCCCCCCGGCGGGGGCGGGGCGGGCCGGG T G UNC93B1 Ensembl:ENSG00000110057 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:68003896..68004075 26863196 MeRIP-seq:(Medium) rs541882491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95864,RMVar_hsa_circ_151099 57283 RMVar_ID_57283 Human_SNP_ID_470747322 m1A Human chr11 - 68014966 68014966 68014966 TGCTCCACCACAGCCCCCGAGGGTGAGCAGGCAGGCAGAGCGCCATGCTTCTTCCTGCCGCACAG TGCTCCACCACAGCCCCCGAGGGTGAGCAGGCGGGCAGAGCGCCATGCTTCTTCCTGCCGCACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:68014955..68015178;chr11:68014953..68015556 26863196 MeRIP-seq:(Medium) rs951605678 Functional Loss SNV dbSNP153 33..33 33 - - - 57284 RMVar_ID_57284 Human_SNP_ID_470747403 m1A Human chr11 - 68015299 68015299 68015299 GCAGTCGCCGCAGCGTGTCCCCAAGGGGGTCCATCCTGCCAGATGGGGTGGCATGAACTGGGTGG GCAGTCGCCGCAGCGTGTCCCCAAGGGGGTCCTTCCTGCCAGATGGGGTGGCATGAACTGGGTGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68008570..68015597 26863196 MeRIP-seq:(Medium) rs1381771500 Functional Loss SNV dbSNP153 33..33 33 - - - 57285 RMVar_ID_57285 Human_SNP_ID_470747404 m1A Human chr11 - 68015299 68015299 68015299 GCAGTCGCCGCAGCGTGTCCCCAAGGGGGTCCATCCTGCCAGATGGGGTGGCATGAACTGGGTGG GCAGTCGCCGCAGCGTGTCCCCAAGGGGGTCCGTCCTGCCAGATGGGGTGGCATGAACTGGGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68008570..68015597 26863196 MeRIP-seq:(Medium) rs1381771500 Functional Loss SNV dbSNP153 33..33 33 - - - 57286 RMVar_ID_57286 Human_SNP_ID_470747431 m1A Human chr11 - 68015340 68015340 68015340 GAACTCAGCTGGCCGCGTGCGCCCCGCGTGGAAGGCCTCCCGCAGTCGCCGCAGCGTGTCCCCAA GAACTCAGCTGGCCGCGTGCGCCCCGCGTGGATGGCCTCCCGCAGTCGCCGCAGCGTGTCCCCAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:68015223..68015375 26863196 MeRIP-seq:(Medium) rs1466738372 Functional Loss SNV dbSNP153 33..33 33 - - - 57287 RMVar_ID_57287 Human_SNP_ID_470747949 m1A Human chr11 + 68017114 68017114 68017114 GAAGAGGCTCAGAGAGAGTGTGTTCTTGCCCAAGGGCATGCAGCCAGGAAGAGCAGAGCCAGAGT GAAGAGGCTCAGAGAGAGTGTGTTCTTGCCCAGGGGCATGCAGCCAGGAAGAGCAGAGCCAGAGT A G ALDH3B1 Ensembl:ENSG00000006534 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68017108..68017218 26863196 MeRIP-seq:(Medium) rs1313225045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_894 57288 RMVar_ID_57288 Human_SNP_ID_470748589 m1A Human chr11 + 68019209 68019209 68019209 TGTGGTGCTGAAGCCATCGGAGATTAGCAAGAACGTCGAGAAGATCCTGGCCGAGGTGCTGCCCC TGTGGTGCTGAAGCCATCGGAGATTAGCAAGACCGTCGAGAAGATCCTGGCCGAGGTGCTGCCCC A C ALDH3B1 Ensembl:ENSG00000006534 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68019176..68019305 26863196 MeRIP-seq:(Medium) rs780048887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5554432 Human_Splice_Rec_1267728,Human_Splice_Rec_1267729,Human_Splice_Rec_1267746,Human_Splice_Rec_1267747,Human_Splice_Rec_1267758,Human_Splice_Rec_1267759,Human_Splice_Rec_1267774,Human_Splice_Rec_1267775,Human_Splice_Rec_1267792,Human_Splice_Rec_1267793,Human_Splice_Rec_1267806,Human_Splice_Rec_1267807,Human_Splice_Rec_1267824,Human_Splice_Rec_1267825,Human_Splice_Rec_1267834,Human_Splice_Rec_1267835,Human_Splice_Rec_1267847 RMVar_hsa_circ_894 57289 RMVar_ID_57289 Human_SNP_ID_470748764 m1A Human chr11 + 68019765 68019765 68019765 CTGGGCGGGCCCCAGGAGACGGGGCAGCTGCTAGAGCACAGGTTCGACTACATCTTCTTCACAGG CTGGGCGGGCCCCAGGAGACGGGGCAGCTGCTGGAGCACAGGTTCGACTACATCTTCTTCACAGG A G ALDH3B1 Ensembl:ENSG00000006534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68019670..68019867 26863196 MeRIP-seq:(Medium) rs751814182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1267730,Human_Splice_Rec_1267731,Human_Splice_Rec_1267748,Human_Splice_Rec_1267749,Human_Splice_Rec_1267760,Human_Splice_Rec_1267761,Human_Splice_Rec_1267776,Human_Splice_Rec_1267777,Human_Splice_Rec_1267808,Human_Splice_Rec_1267809,Human_Splice_Rec_1267826,Human_Splice_Rec_1267827,Human_Splice_Rec_1267848,Human_Splice_Rec_1267849 57290 RMVar_ID_57290 Human_SNP_ID_470749254 m1A Human chr11 + 68021565 68021565 68021565 TGACACCTGTCACCCTGGAGCTGGGGGGCAAGAACCCTTGCTACGTGGACGACAACTGCGACCCC TGACACCTGTCACCCTGGAGCTGGGGGGCAAGCACCCTTGCTACGTGGACGACAACTGCGACCCC A C ALDH3B1 Ensembl:ENSG00000006534 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68019192..68021650 32194978 MeRIP-seq:(Medium) rs1166768281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108318 Human_Splice_Rec_1267732,Human_Splice_Rec_1267750,Human_Splice_Rec_1267762,Human_Splice_Rec_1267778,Human_Splice_Rec_1267794,Human_Splice_Rec_1267810,Human_Splice_Rec_1267828,Human_Splice_Rec_1267850 57291 RMVar_ID_57291 Human_SNP_ID_470749257 m1A Human chr11 - 68021570 68021570 68021570 GTCTGGGGGTCGCAGTTGTCGTCCACGTAGCAAGGGTTCTTGCCCCCCAGCTCCAGGGTGACAGG GTCTGGGGGTCGCAGTTGTCGTCCACGTAGCAGGGGTTCTTGCCCCCCAGCTCCAGGGTGACAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68021443..68021804 26863196 MeRIP-seq:(Medium) rs745850732 Functional Loss SNV dbSNP153 33..33 33 - - - 57292 RMVar_ID_57292 Human_SNP_ID_470749343 m1A Human chr11 - 68021738 68021738 68021738 CCCAGGTTTGGGGAGCTCTGGGGGTCGTCGCCATAGAAACGGGTGATGGTGCTCTGCAGGGCAGG CCCAGGTTTGGGGAGCTCTGGGGGTCGTCGCCGTAGAAACGGGTGATGGTGCTCTGCAGGGCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68021688..68022661 32194978 MeRIP-seq:(Medium) rs770077903 Functional Loss SNV dbSNP153 33..33 33 - - - 57293 RMVar_ID_57293 Human_SNP_ID_470751020 m1A Human chr11 - 68027854 68027854 68027854 TCAGGCGGCGCGGCGATTGCGGCGGGTAGCGGAGGGCGTTGAGCTTCTCCATCCCCGGGCTGCGC TCAGGCGGCGCGGCGATTGCGGCGGGTAGCGGGGGGCGTTGAGCTTCTCCATCCCCGGGCTGCGC T C AC004923.4 Ensembl:ENSG00000255306 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68027805..68027967 26863196 MeRIP-seq:(Medium) rs1203586105 Functional Loss SNV dbSNP153 33..33 33 - - - 57294 RMVar_ID_57294 Human_SNP_ID_470751178 m1A Human chr11 + 68028137 68028137 68028137 GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCATGAGAGCCGAGGTGGGAGGCATGGGAAACAGT GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCCTGAGAGCCGAGGTGGGAGGCATGGGAAACAGT A C ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68028086..68028186 32194978 MeRIP-seq:(Medium) rs536699902 Functional Loss SNV dbSNP153 33..33 33 - - - 57295 RMVar_ID_57295 Human_SNP_ID_470751179 m1A Human chr11 + 68028137 68028137 68028137 GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCATGAGAGCCGAGGTGGGAGGCATGGGAAACAGT GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCGTGAGAGCCGAGGTGGGAGGCATGGGAAACAGT A G ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68028086..68028186 32194978 MeRIP-seq:(Medium) rs536699902 Functional Loss SNV dbSNP153 33..33 33 - - - 57296 RMVar_ID_57296 Human_SNP_ID_470751180 m1A Human chr11 + 68028137 68028137 68028137 GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCATGAGAGCCGAGGTGGGAGGCATGGGAAACAGT GCCTCAGCCTCCTCCCTCAGCCGCTCCCAACCTTGAGAGCCGAGGTGGGAGGCATGGGAAACAGT A T ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68028086..68028186 32194978 MeRIP-seq:(Medium) rs536699902 Functional Loss SNV dbSNP153 33..33 33 - - - 57297 RMVar_ID_57297 Human_SNP_ID_470751271 m1A Human chr11 - 68028473 68028473 68028473 GGGGTTTCGCCATGTTAGCCAGGCTGATCTTGAACTCCTGATTTCAGGTGATCCGCCTGCCTCGG GGGGTTTCGCCATGTTAGCCAGGCTGATCTTGGACTCCTGATTTCAGGTGATCCGCCTGCCTCGG T C AC004923.4 Ensembl:ENSG00000255306 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68028434..68028535 32194978 MeRIP-seq:(Medium) rs1199935603 Functional Loss SNV dbSNP153 33..33 33 - - - 57298 RMVar_ID_57298 Human_SNP_ID_470751334 m1A Human chr11 + 68028682 68028676 68028682 CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAAAAAAAAAAAAAAAAACCTCCTGGGACTGTTGCA CTGGGTGACAGAAGGAGGCTCTGCCTT______AAAAAAAAAAAAAACCTCCTGGGACTGTTGCA TAAAAAA T ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68028633..68029009 26863196 MeRIP-seq:(Medium) rs10557779 Functional Loss DEL dbSNP153 28..33 33 - - - 57299 RMVar_ID_57299 Human_SNP_ID_470751335 m1A Human chr11 + 68028682 68028676 68028682 CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAAAAAAAAAAAAAAAAACCTCCTGGGACTGTTGCA CTGGGTGACAGAAGGAGGCTCTGCCTTAA____AAAAAAAAAAAAAACCTCCTGGGACTGTTGCA TAAAAAA TAA ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68028633..68029009 26863196 MeRIP-seq:(Medium) rs10557779 Functional Loss DEL dbSNP153 30..33 33 - - - 57300 RMVar_ID_57300 Human_SNP_ID_470751336 m1A Human chr11 + 68028682 68028676 68028682 CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAAAAAAAAAAAAAAAAACCTCCTGGGACTGTTGCA CTGGGTGACAGAAGGAGGCTCTGCCTTAAA___AAAAAAAAAAAAAACCTCCTGGGACTGTTGCA TAAAAAA TAAA ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68028633..68029009 26863196 MeRIP-seq:(Medium) rs10557779 Functional Loss DEL dbSNP153 31..33 33 - - - 57301 RMVar_ID_57301 Human_SNP_ID_470751337 m1A Human chr11 + 68028682 68028676 68028682 CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAAAAAAAAAAAAAAAAACCTCCTGGGACTGTTGCA CTGGGTGACAGAAGGAGGCTCTGCCTTAAAA__AAAAAAAAAAAAAACCTCCTGGGACTGTTGCA TAAAAAA TAAAA ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68028633..68029009 26863196 MeRIP-seq:(Medium) rs10557779 Functional Loss DEL dbSNP153 32..33 33 - - - 57302 RMVar_ID_57302 Human_SNP_ID_470751338 m1A Human chr11 + 68028682 68028676 68028682 CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAAAAAAAAAAAAAAAAACCTCCTGGGACTGTTGCA CTGGGTGACAGAAGGAGGCTCTGCCTTAAAAA_AAAAAAAAAAAAAACCTCCTGGGACTGTTGCA TAAAAAA TAAAAA ALDH3B1 Ensembl:ENSG00000006534 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68028633..68029009 26863196 MeRIP-seq:(Medium) rs10557779 Functional Loss DEL dbSNP153 33..33 33 - - - 57303 RMVar_ID_57303 Human_SNP_ID_470751999 m1A Human chr11 + 68030731 68030731 68030731 CTGCTTGGCAAGGCAAGTAGCGGCGGCGCTTCAAGGTGGGTGTTCACGTTTTGGCCGTGAAAGTC CTGCTTGGCAAGGCAAGTAGCGGCGGCGCTTCGAGGTGGGTGTTCACGTTTTGGCCGTGAAAGTC A G NDUFS8 Ensembl:ENSG00000110717 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1418462750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_988209,Human_RBP_ID_4185205,Human_RBP_ID_5110929,Human_RBP_ID_9321661,Human_RBP_ID_19050093,Human_RBP_ID_27804792 Human_Splice_Rec_1267859,Human_Splice_Rec_1267867,Human_Splice_Rec_1267869,Human_Splice_Rec_1267879,Human_Splice_Rec_1267889,Human_Splice_Rec_1267899,Human_Splice_Rec_1267901 RMVar_hsa_circ_79704,RMVar_hsa_circ_151101 57304 RMVar_ID_57304 Human_SNP_ID_470752000 m1A Human chr11 - 68030735 68030735 68030735 GCCCGACTTTCACGGCCAAAACGTGAACACCCACCTTGAAGCGCCGCCGCTACTTGCCTTGCCAA GCCCGACTTTCACGGCCAAAACGTGAACACCCCCCTTGAAGCGCCGCCGCTACTTGCCTTGCCAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:68030676..68030989;chr11:68030666..68030978;chr11:68030626..68031010;chr11:68030676..68030859;chr11:68030676..68031027 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs904008036 Functional Loss SNV dbSNP153 33..33 33 - - - 57305 RMVar_ID_57305 Human_SNP_ID_470752333 m1A Human chr11 - 68031808 68031808 68031808 CATCCTCCCCAAATCTAACCAAAAACAACATTACCAGCCCCCGCCAGCATGCACTGAGAGCGAAC CATCCTCCCCAAATCTAACCAAAAACAACATTGCCAGCCCCCGCCAGCATGCACTGAGAGCGAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68031804..68031984 26863196 MeRIP-seq:(Medium) rs1258782690 Functional Loss SNV dbSNP153 33..33 33 - - - 57306 RMVar_ID_57306 Human_SNP_ID_470753862 m1A Human chr11 + 68036301 68036301 68036301 CTGAGCCAAGAGCTGATGGCAGCCGCCGGACCACCCGCTATGACATCGACATGACCAAGTGCATC CTGAGCCAAGAGCTGATGGCAGCCGCCGGACCCCCCGCTATGACATCGACATGACCAAGTGCATC A C NDUFS8 Ensembl:ENSG00000110717 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68036214..68036608 26863196 MeRIP-seq:(Medium) rs1217820452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402207,Human_RBP_ID_865327,Human_RBP_ID_4175737,Human_RBP_ID_5110552,Human_RBP_ID_17649788,Human_RBP_ID_26803918 Human_Splice_Rec_1267888,Human_Splice_Rec_1267898,Human_Splice_Rec_1267900,Human_Splice_Rec_1267922,Human_Splice_Rec_1267928,Human_Splice_Rec_1267948,Human_Splice_Rec_1267950 RMVar_hsa_circ_15030,RMVar_hsa_circ_79704,RMVar_hsa_circ_151101,RMVar_hsa_circ_91696,RMVar_hsa_circ_128022,RMVar_hsa_circ_151104,RMVar_hsa_circ_119067,RMVar_hsa_circ_151105,RMVar_hsa_circ_151106 57307 RMVar_ID_57307 Human_SNP_ID_470753996 m1A Human chr11 + 68036553 68036553 68036553 GTTGCTCAACAACGGGGACAAGTGGGAGGCCGAGATCGCCGCCAACATCCAGGCTGACTACTTGT GTTGCTCAACAACGGGGACAAGTGGGAGGCCGGGATCGCCGCCAACATCCAGGCTGACTACTTGT A G NDUFS8 Ensembl:ENSG00000110717 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68036451..68036650 32194978 MeRIP-seq:(Medium) rs894226009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402216,Human_RBP_ID_1459829,Human_RBP_ID_9005770,Human_RBP_ID_17649219 RMVar_hsa_circ_79704,RMVar_hsa_circ_151101,RMVar_hsa_circ_108670,RMVar_hsa_circ_91696,RMVar_hsa_circ_128022,RMVar_hsa_circ_151104,RMVar_hsa_circ_119067,RMVar_hsa_circ_151105,RMVar_hsa_circ_151106,RMVar_hsa_circ_151107 57308 RMVar_ID_57308 Human_SNP_ID_470755767 m1A Human chr11 - 68042682 68042682 68042682 GGGGTGCCGGCAGCCTCCCCTTTGGCGGGGGCAGGACCAGCCCAGCCCGCCGCACCTCCTCCTGC GGGGTGCCGGCAGCCTCCCCTTTGGCGGGGGCGGGACCAGCCCAGCCCGCCGCACCTCCTCCTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68041291..68043196 32194978 MeRIP-seq:(Medium) rs1489611026 Functional Loss SNV dbSNP153 33..33 33 - - - 57309 RMVar_ID_57309 Human_SNP_ID_470755804 m1A Human chr11 + 68042745 68042745 68042745 CCCACCCCGGGACCTGCTGCGCATCCAGGAGGAGACGGAGCGCCTGGCCCAGGAGCTGCGGGATG CCCACCCCGGGACCTGCTGCGCATCCAGGAGGTGACGGAGCGCCTGGCCCAGGAGCTGCGGGATG A T TCIRG1 Ensembl:ENSG00000110719 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68042626..68043266 26863196 MeRIP-seq:(Medium) rs993860020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30061,Human_RBP_ID_3940967,Human_RBP_ID_9363928,Human_RBP_ID_18972411,Human_RBP_ID_22433813,Human_RBP_ID_22895186,Human_RBP_ID_26318892 RMVar_hsa_circ_76889,RMVar_hsa_circ_82679,RMVar_hsa_circ_113110,RMVar_hsa_circ_151108,RMVar_hsa_circ_151110,RMVar_hsa_circ_125031,RMVar_hsa_circ_151111,RMVar_hsa_circ_151112,RMVar_hsa_circ_93009,RMVar_hsa_circ_151113 57310 RMVar_ID_57310 Human_SNP_ID_470756199 m1A Human chr11 + 68043640 68043640 68043640 ACTGGGGTGAGCAGATCGGACAGAAGATCCGCAAGATCACGGACTGGTGAGTCACTGGGAACACC ACTGGGGTGAGCAGATCGGACAGAAGATCCGCCAGATCACGGACTGGTGAGTCACTGGGAACACC A C TCIRG1 Ensembl:ENSG00000110719 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68043575..68043649 26863196 MeRIP-seq:(Medium) rs1376740807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939588,Human_RBP_ID_9363934,Human_RBP_ID_18972416 Human_Splice_Rec_1267962,Human_Splice_Rec_1267963,Human_Splice_Rec_1267998,Human_Splice_Rec_1267999,Human_Splice_Rec_1268014,Human_Splice_Rec_1268015,Human_Splice_Rec_1268032,Human_Splice_Rec_1268042,Human_Splice_Rec_1268044,Human_Splice_Rec_1268045,Human_Splice_Rec_1268071,Human_Splice_Rec_1268076,Human_Splice_Rec_1268077 RMVar_hsa_circ_76889,RMVar_hsa_circ_82679,RMVar_hsa_circ_113110,RMVar_hsa_circ_151108,RMVar_hsa_circ_151110,RMVar_hsa_circ_125031,RMVar_hsa_circ_89146,RMVar_hsa_circ_116828,RMVar_hsa_circ_151111,RMVar_hsa_circ_151112,RMVar_hsa_circ_93009,RMVar_hsa_circ_151113,RMVar_hsa_circ_127776,RMVar_hsa_circ_151114,RMVar_hsa_circ_111123,RMVar_hsa_circ_151115,RMVar_hsa_circ_151116,RMVar_hsa_circ_151117 57311 RMVar_ID_57311 Human_SNP_ID_470756466 m1A Human chr11 + 68044184 68044181 68044184 GTTCCTGAGCCAGGTGCTAGGCCGGGTGCTGCAGCTGCTGCCGCCAGGGCAGGTGCAGGTCCACA GTTCCTGAGCCAGGTGCTAGGCCGGGTGCT___GCTGCTGCCGCCAGGGCAGGTGCAGGTCCACA TGCA T TCIRG1 Ensembl:ENSG00000110719 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68044112..68044366 26863196 MeRIP-seq:(Medium) rs1309487984 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3093,Human_RBP_ID_867947,Human_RBP_ID_3939590,Human_RBP_ID_5111210,Human_RBP_ID_9362638,Human_RBP_ID_18468977,Human_RBP_ID_18972418,Human_RBP_ID_22434687,Human_RBP_ID_22895449,Human_RBP_ID_23207383,Human_RBP_ID_26318895,Human_RBP_ID_26767962,Human_RBP_ID_27803726 Human_Splice_Rec_1267966,Human_Splice_Rec_1268002,Human_Splice_Rec_1268018,Human_Splice_Rec_1268048,Human_Splice_Rec_1268074,Human_Splice_Rec_1268080,Human_Splice_Rec_1268088 RMVar_hsa_circ_76889,RMVar_hsa_circ_82679,RMVar_hsa_circ_113110,RMVar_hsa_circ_151108,RMVar_hsa_circ_151110,RMVar_hsa_circ_89146,RMVar_hsa_circ_116828,RMVar_hsa_circ_151112,RMVar_hsa_circ_93009,RMVar_hsa_circ_151113,RMVar_hsa_circ_127776,RMVar_hsa_circ_151114,RMVar_hsa_circ_111123,RMVar_hsa_circ_151115,RMVar_hsa_circ_126377,RMVar_hsa_circ_151116,RMVar_hsa_circ_151117,RMVar_hsa_circ_109651,RMVar_hsa_circ_151118,RMVar_hsa_circ_151119 57312 RMVar_ID_57312 Human_SNP_ID_470757728 m1A Human chr11 - 68047690 68047690 68047690 AGATGAAGCCGGTGTAGATGGAGAACAGGCCCATAAGCAGGAGCAGGTAGCGGCCCCTGAAGAAA AGATGAAGCCGGTGTAGATGGAGAACAGGCCCCTAAGCAGGAGCAGGTAGCGGCCCCTGAAGAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68047567..68047742 26863196 MeRIP-seq:(Medium) rs1348842114 Functional Loss SNV dbSNP153 33..33 33 - - - 57313 RMVar_ID_57313 Human_SNP_ID_470757875 m1A Human chr11 - 68047974 68047974 68047974 TCACCACCCACGGACACTCCATCCCAGGACTCACAGGATCGATGCCAAAGGGGTAGGGTCCCAGG TCACCACCCACGGACACTCCATCCCAGGACTCTCAGGATCGATGCCAAAGGGGTAGGGTCCCAGG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68047951..68047975 32194978 MeRIP-seq:(Medium) rs761918801 Functional Loss SNV dbSNP153 33..33 33 - - - 57314 RMVar_ID_57314 Human_SNP_ID_470758209 m1A Human chr11 - 68048999 68048999 68048999 AGCCTCCCGTCCCCCGGGCAGCCTTGGCCCTCACACGTGGTTGAAGACTCCGAGGACCACCCCAA AGCCTCCCGTCCCCCGGGCAGCCTTGGCCCTCGCACGTGGTTGAAGACTCCGAGGACCACCCCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68048948..68049281 32194978 MeRIP-seq:(Medium) rs747048627 Functional Loss SNV dbSNP153 33..33 33 - - - 57315 RMVar_ID_57315 Human_SNP_ID_470758331 m1A Human chr11 - 68049278 68049278 68049278 ACCAGCCGCAGCCCACCTGCCGGGGGTAGAGCAGCCTGTTGCTGGGGCTGTGGGAGAAGAGGAAC ACCAGCCGCAGCCCACCTGCCGGGGGTAGAGCGGCCTGTTGCTGGGGCTGTGGGAGAAGAGGAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68049227..68049329 26863196 MeRIP-seq:(Medium) rs748503466 Functional Loss SNV dbSNP153 33..33 33 - - - 57316 RMVar_ID_57316 Human_SNP_ID_470758653 m1A Human chr11 - 68049994 68049994 68049994 TCATCGGAGCTCCAGCCATTCACAGATGCGTCAGGCAGGTCCAGCAACCCGGCCTTGTTTTCCTC TCATCGGAGCTCCAGCCATTCACAGATGCGTCGGGCAGGTCCAGCAACCCGGCCTTGTTTTCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68049962..68050037 26863196 MeRIP-seq:(Medium) rs373493580 Functional Loss SNV dbSNP153 33..33 33 - - - 57317 RMVar_ID_57317 Human_SNP_ID_470758932 m1A Human chr11 - 68050568 68050568 68050568 TCATCACGGCAAAGGCGGCAAAGATGGGGACCAGCACCACAGCCGCCACGCCCACCTCCCGGCCC TCATCACGGCAAAGGCGGCAAAGATGGGGACCGGCACCACAGCCGCCACGCCCACCTCCCGGCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68050519..68050885 32194978 MeRIP-seq:(Medium) rs765495869 Functional Loss SNV dbSNP153 33..33 33 - - - 57318 RMVar_ID_57318 Human_SNP_ID_470759340 m1A Human chr11 + 68051945 68051945 68051945 GGAGGGGTGCAGTGTGGGATCCCAGGGACATGACCAGTCAGCCCCGCCCTGGCTTTGACATGGGG GGAGGGGTGCAGTGTGGGATCCCAGGGACATGCCCAGTCAGCCCCGCCCTGGCTTTGACATGGGG A C AP002807.1 Ensembl:ENSG00000255031 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:68051895..68052121 26863196 MeRIP-seq:(Medium) rs1285970890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3389024,Human_RBP_ID_9415062 57319 RMVar_ID_57319 Human_SNP_ID_470759826 m1A Human chr11 + 68053408 68053408 68053408 GCTCCACACGCTGGCGGCCTTGGCTGCTCCAGAGCAATCCGCTGCTCCAGCTTCAGCCATGGGAC GCTCCACACGCTGGCGGCCTTGGCTGCTCCAGGGCAATCCGCTGCTCCAGCTTCAGCCATGGGAC A G AP002807.1 Ensembl:ENSG00000255031 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68053053..68053505 32194978 MeRIP-seq:(Medium) rs1362981230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1268160,Human_Splice_Rec_1268164,Human_Splice_Rec_1268166 57320 RMVar_ID_57320 Human_SNP_ID_470765233 m1A Human chr11 - 68074741 68074741 68074741 CTTGGGCCAAAACTCTATGGCATCTTTCCCCAAGGCCGACTGGAGCAGTTCATCCCGGTAAGATT CTTGGGCCAAAACTCTATGGCATCTTTCCCCACGGCCGACTGGAGCAGTTCATCCCGGTAAGATT T G CHKA Ensembl:ENSG00000110721 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68070733..68074742 32194978 MeRIP-seq:(Medium) rs760667062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_988213,Human_RBP_ID_9362639,Human_RBP_ID_18433118,Human_RBP_ID_18972432,Human_RBP_ID_19050112 Human_Splice_Rec_1268172,Human_Splice_Rec_1268173,Human_Splice_Rec_1268204,Human_Splice_Rec_1268205,Human_Splice_Rec_1268222,Human_Splice_Rec_1268223,Human_Splice_Rec_1268236,Human_Splice_Rec_1268237,Human_Splice_Rec_1268250,Human_Splice_Rec_1268251,Human_Splice_Rec_1268258,Human_Splice_Rec_1268259 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_11874,RMVar_hsa_circ_151131,RMVar_hsa_circ_290829,RMVar_hsa_circ_357675,RMVar_hsa_circ_61492,RMVar_hsa_circ_151132,RMVar_hsa_circ_320988,RMVar_hsa_circ_333132,RMVar_hsa_circ_151133,RMVar_hsa_circ_61142,RMVar_hsa_circ_336836 57321 RMVar_ID_57321 Human_SNP_ID_470773477 m1A Human chr11 - 68107415 68107415 68107415 GAAGAAATTATTTTGAATAGAGGAAGGAAAAGATTATAAGTTGGGAATCAAGTTAGAGAACAAAT GAAGAAATTATTTTGAATAGAGGAAGGAAAAGTTTATAAGTTGGGAATCAAGTTAGAGAACAAAT T A CHKA Ensembl:ENSG00000110721 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68107411..68107538 26863196 MeRIP-seq:(Medium) rs1475553125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98826,RMVar_hsa_circ_151131 57322 RMVar_ID_57322 Human_SNP_ID_470773478 m1A Human chr11 - 68107415 68107415 68107415 GAAGAAATTATTTTGAATAGAGGAAGGAAAAGATTATAAGTTGGGAATCAAGTTAGAGAACAAAT GAAGAAATTATTTTGAATAGAGGAAGGAAAAGGTTATAAGTTGGGAATCAAGTTAGAGAACAAAT T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68107411..68107538 26863196 MeRIP-seq:(Medium) rs1475553125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98826,RMVar_hsa_circ_151131 57323 RMVar_ID_57323 Human_SNP_ID_470777185 m1A Human chr11 - 68120951 68120951 68120951 GCCGCTGCCGCTGCCCCAGCCCCCGCCGCCGCAGCCGCCCGCAGACGAGCAGCCGGAGCCCCGGA GCCGCTGCCGCTGCCCCAGCCCCCGCCGCCGCCGCCGCCCGCAGACGAGCAGCCGGAGCCCCGGA T G CHKA Ensembl:ENSG00000110721 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68120911..68120982 26863196 MeRIP-seq:(Medium) rs749538147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98826,RMVar_hsa_circ_151131 57324 RMVar_ID_57324 Human_SNP_ID_470777347 m1A Human chr11 - 68121328 68121319 68121328 CATCCCCGCTCCACAGTCGCCGCAGTCGCCGCAGCCGCCGCCGCCGCCCCGCGCGCCCAACCGCC CATCCCCGCTCCACAGTCGCCGCAGTCGCCGC_________CGCCGCCCCGCGCGCCCAACCGCC GGCGGCGGCT G CHKA Ensembl:ENSG00000110721 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:68120797..68121370;chr11:68121091..68121375 26863196 MeRIP-seq:(Medium) rs1167438959 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4185216,Human_RBP_ID_5345880,Human_RBP_ID_9321667,Human_RBP_ID_9363947 RMVar_hsa_circ_98826,RMVar_hsa_circ_151131 57325 RMVar_ID_57325 Human_SNP_ID_470777367 m1A Human chr11 - 68121328 68121328 68121328 CATCCCCGCTCCACAGTCGCCGCAGTCGCCGCAGCCGCCGCCGCCGCCCCGCGCGCCCAACCGCC CATCCCCGCTCCACAGTCGCCGCAGTCGCCGCCGCCGCCGCCGCCGCCCCGCGCGCCCAACCGCC T G CHKA Ensembl:ENSG00000110721 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:68120797..68121370;chr11:68121091..68121375 26863196 MeRIP-seq:(Medium) rs1191731753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185216,Human_RBP_ID_5345880,Human_RBP_ID_9321667,Human_RBP_ID_9363947 RMVar_hsa_circ_98826,RMVar_hsa_circ_151131 57326 RMVar_ID_57326 Human_SNP_ID_470777373 m1A Human chr11 + 68121335 68121335 68121335 GGGCGCGCGGGGCGGCGGCGGCGGCTGCGGCGACTGCGGCGACTGTGGAGCGGGGATGTGCTGCT GGGCGCGCGGGGCGGCGGCGGCGGCTGCGGCGGCTGCGGCGACTGTGGAGCGGGGATGTGCTGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:68121235..68121368;chr11:68121176..68121400;chr11:68121151..68121400 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1216249311 Functional Loss SNV dbSNP153 33..33 33 - - - 57327 RMVar_ID_57327 Human_SNP_ID_470801189 m1A Human chr11 - 68213108 68213108 68213108 GCGGTGAGTCGGGGGAGGGGCGGGCGCCGGCGAGGGTGTGCGGGGGGCGGCCTCGGTGACGGGGC GCGGTGAGTCGGGGGAGGGGCGGGCGCCGGCGGGGGTGTGCGGGGGGCGGCCTCGGTGACGGGGC T C KMT5B Ensembl:ENSG00000110066 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68213105..68213241 26863196 MeRIP-seq:(Medium) rs1400212619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8174465,Human_RBP_ID_26776513 RMVar_hsa_circ_151136,RMVar_hsa_circ_123985 57328 RMVar_ID_57328 Human_SNP_ID_470801500 m1A Human chr11 - 68213564 68213564 68213564 GGGGCGATGAGGTGAGGACGCCCGGGAACCGGAGGCGGCACCGCGCGGCGCACGGACCTGGGACG GGGGCGATGAGGTGAGGACGCCCGGGAACCGGTGGCGGCACCGCGCGGCGCACGGACCTGGGACG T A KMT5B Ensembl:ENSG00000110066 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68213425..68213816 26863196 MeRIP-seq:(Medium) rs544069083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752029,Human_RBP_ID_9321669,Human_RBP_ID_18416609,Human_RBP_ID_22895190 Human_Splice_Rec_1268363,Human_Splice_Rec_1268381,Human_Splice_Rec_1268401,Human_Splice_Rec_1268449,Human_Splice_Rec_1268461 57329 RMVar_ID_57329 Human_SNP_ID_470801501 m1A Human chr11 - 68213564 68213564 68213564 GGGGCGATGAGGTGAGGACGCCCGGGAACCGGAGGCGGCACCGCGCGGCGCACGGACCTGGGACG GGGGCGATGAGGTGAGGACGCCCGGGAACCGGGGGCGGCACCGCGCGGCGCACGGACCTGGGACG T C KMT5B Ensembl:ENSG00000110066 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68213425..68213816 26863196 MeRIP-seq:(Medium) rs544069083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752029,Human_RBP_ID_9321669,Human_RBP_ID_18416609,Human_RBP_ID_22895190 Human_Splice_Rec_1268363,Human_Splice_Rec_1268381,Human_Splice_Rec_1268401,Human_Splice_Rec_1268449,Human_Splice_Rec_1268461 57330 RMVar_ID_57330 Human_SNP_ID_470801502 m1A Human chr11 - 68213564 68213564 68213564 GGGGCGATGAGGTGAGGACGCCCGGGAACCGGAGGCGGCACCGCGCGGCGCACGGACCTGGGACG GGGGCGATGAGGTGAGGACGCCCGGGAACCGGCGGCGGCACCGCGCGGCGCACGGACCTGGGACG T G KMT5B Ensembl:ENSG00000110066 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68213425..68213816 26863196 MeRIP-seq:(Medium) rs544069083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752029,Human_RBP_ID_9321669,Human_RBP_ID_18416609,Human_RBP_ID_22895190 Human_Splice_Rec_1268363,Human_Splice_Rec_1268381,Human_Splice_Rec_1268401,Human_Splice_Rec_1268449,Human_Splice_Rec_1268461 57331 RMVar_ID_57331 Human_SNP_ID_470814785 m1A Human chr11 - 68262118 68262118 68262118 CAGAGCCCGCCCCCACCCCCACAGTGGTGACCACCACCAAGGCACAAGCCAGGGAGCCAACTGCC CAGAGCCCGCCCCCACCCCCACAGTGGTGACCGCCACCAAGGCACAAGCCAGGGAGCCAACTGCC T C C11orf24 Ensembl:ENSG00000171067 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68262025..68262125 32194978 MeRIP-seq:(Medium) rs1391085929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17350283,Human_RBP_ID_27206266 57332 RMVar_ID_57332 Human_SNP_ID_470814952 m1A Human chr11 - 68262487 68262487 68262487 GCACTCCCATGACACTTGCACTCCCCGCGCCCACGTCCACTTCCACAGGGCGGACCCCGTCCACT GCACTCCCATGACACTTGCACTCCCCGCGCCCGCGTCCACTTCCACAGGGCGGACCCCGTCCACT T C C11orf24 Ensembl:ENSG00000171067 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:68262436..68262687 26863196 MeRIP-seq:(Medium) rs1337568833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227925,Human_RBP_ID_5126689,Human_RBP_ID_17235253,Human_RBP_ID_17350284,Human_RBP_ID_18932665,Human_RBP_ID_22034781,Human_RBP_ID_26896155,Human_RBP_ID_27206270 57333 RMVar_ID_57333 Human_SNP_ID_470816631 m1A Human chr11 - 68268191 68268191 68268191 ACCTTCGTCTCACATGTGCCACAAAGGATGGCATGGCCCGGGAGTGCCCCACCACGTGGCTTTCA ACCTTCGTCTCACATGTGCCACAAAGGATGGCGTGGCCCGGGAGTGCCCCACCACGTGGCTTTCA T C C11orf24 Ensembl:ENSG00000171067 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68268140..68268239 32194978 MeRIP-seq:(Medium) rs1001353390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32593,Human_RBP_ID_752404,Human_RBP_ID_4184281,Human_RBP_ID_5111214,Human_RBP_ID_27206282,Human_RBP_ID_27804798 Human_Splice_Rec_1268464,Human_Splice_Rec_1268472,Human_Splice_Rec_1268480,Human_Splice_Rec_1268486,Human_Splice_Rec_1268490,Human_Splice_Rec_1268494,Human_Splice_Rec_1268498,Human_Splice_Rec_1268502 RMVar_hsa_circ_20798,RMVar_hsa_circ_316180 57334 RMVar_ID_57334 Human_SNP_ID_470827547 m1A Human chr11 + 68312646 68312624 68312646 AGGGGGGAGGCGGAGGCGCCGGGAGCCGCGCGAGGAGCCGCCGCCGCCGCGCCATGGAGCCCGAG AGGGGGGAGGC______________________GGAGCCGCCGCCGCCGCGCCATGGAGCCCGAG CGGAGGCGCCGGGAGCCGCGCGA C LRP5 Ensembl:ENSG00000162337 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:68312513..68312890;chr11:68312518..68312880 26863196 MeRIP-seq:(Medium) rs1329119348 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_4175928,Human_RBP_ID_9275992,Human_RBP_ID_9321671,Human_RBP_ID_18478052,Human_RBP_ID_26776516 RMVar_hsa_circ_151160,RMVar_hsa_circ_120751 57335 RMVar_ID_57335 Human_SNP_ID_470827550 m1A Human chr11 + 68312646 68312634 68312646 AGGGGGGAGGCGGAGGCGCCGGGAGCCGCGCGAGGAGCCGCCGCCGCCGCGCCATGGAGCCCGAG AGGGGGGAGGCGGAGGCGCCG____________GGAGCCGCCGCCGCCGCGCCATGGAGCCCGAG GGGAGCCGCGCGA G LRP5 Ensembl:ENSG00000162337 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:68312513..68312890;chr11:68312518..68312880 26863196 MeRIP-seq:(Medium) rs1214520652 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4175928,Human_RBP_ID_9275992,Human_RBP_ID_9321671,Human_RBP_ID_18478052,Human_RBP_ID_26776516 RMVar_hsa_circ_151160,RMVar_hsa_circ_120751 57336 RMVar_ID_57336 Human_SNP_ID_470832855 m1A Human chr11 + 68334255 68334252 68334256 GACTCCATCTCAAACAAATAAATAAGAAATAAAGAAGCAGCATGTCGAGGGTGGTGCTATGTAGA GACTCCATCTCAAACAAATAAATAAGAAAT____AAGCAGCATGTCGAGGGTGGTGCTATGTAGA TAAAG T LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68334250..68334404 26863196 MeRIP-seq:(Medium) rs1358261541 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_151160,RMVar_hsa_circ_120751 57337 RMVar_ID_57337 Human_SNP_ID_470836436 m1A Human chr11 - 68347958 68347958 68347958 AGTACACGGCTCCCTTGGAAAACTGGAAGTCCACTGCGGCCGCATCCTCCAGGCCGCTGACCACG AGTACACGGCTCCCTTGGAAAACTGGAAGTCCGCTGCGGCCGCATCCTCCAGGCCGCTGACCACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68347908..68348025 26863196 MeRIP-seq:(Medium) rs1464364403 Functional Loss SNV dbSNP153 33..33 33 - - - 57338 RMVar_ID_57338 Human_SNP_ID_470837798 m1A Human chr11 - 68352532 68352532 68352532 TCACCTAGCACCTCCCGACTGATCACCTCCCAACCTAGCACTGAGCACTTCCCAACCAACATAGC TCACCTAGCACCTCCCGACTGATCACCTCCCAGCCTAGCACTGAGCACTTCCCAACCAACATAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68352528..68353023 26863196 MeRIP-seq:(Medium) rs140768342 Functional Loss SNV dbSNP153 33..33 33 - - - 57339 RMVar_ID_57339 Human_SNP_ID_470841235 m1A Human chr11 + 68365690 68365688 68365691 CCACGGGTGTGCAGCTGCAGGACAACGGCAGGACGTGTAAGGCAGGTGAGGCGGTGGGACGGGAC CCACGGGTGTGCAGCTGCAGGACAACGGCAG___GTGTAAGGCAGGTGAGGCGGTGGGACGGGAC GGAC G LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68365640..68365750 26863196 MeRIP-seq:(Medium) rs776221148 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3939594,Human_RBP_ID_5550128,Human_RBP_ID_17805941,Human_RBP_ID_18468985,Human_RBP_ID_27154433 Human_Splice_Rec_1268515,Human_Splice_Rec_1268557 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_280139,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151166,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_293205,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151172,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_119098,RMVar_hsa_circ_151178,RMVar_hsa_circ_151179,RMVar_hsa_circ_151180 57340 RMVar_ID_57340 Human_SNP_ID_470841237 m1A Human chr11 + 68365690 68365690 68365690 CCACGGGTGTGCAGCTGCAGGACAACGGCAGGACGTGTAAGGCAGGTGAGGCGGTGGGACGGGAC CCACGGGTGTGCAGCTGCAGGACAACGGCAGGGCGTGTAAGGCAGGTGAGGCGGTGGGACGGGAC A G LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68365640..68365750 26863196 MeRIP-seq:(Medium) rs764149976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939594,Human_RBP_ID_5550128,Human_RBP_ID_17805941,Human_RBP_ID_18468985,Human_RBP_ID_27154433 Human_Splice_Rec_1268515,Human_Splice_Rec_1268557 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_280139,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151166,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_293205,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151172,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_119098,RMVar_hsa_circ_151178,RMVar_hsa_circ_151179,RMVar_hsa_circ_151180 57341 RMVar_ID_57341 Human_SNP_ID_470842987 m1A Human chr11 + 68372454 68372454 68372454 CCGTGGCGGCGAGGAGGTGCAGCGTCAGGCGGACCCGGGACCGTGGCGGCGAGGAGGTGCAGTGT CCGTGGCGGCGAGGAGGTGCAGCGTCAGGCGGTCCCGGGACCGTGGCGGCGAGGAGGTGCAGTGT A T LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:68372165..68372499;chr11:68372076..68372561;chr11:68372033..68372555;chr11:68372112..68372528 26863196 MeRIP-seq:(Medium) rs314777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_806445,Human_RBP_ID_3386995,Human_RBP_ID_8063678,Human_RBP_ID_8174505,Human_RBP_ID_17111150,Human_RBP_ID_18416957,Human_RBP_ID_22709599 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_151178,RMVar_hsa_circ_151180 57342 RMVar_ID_57342 Human_SNP_ID_470843768 m1A Human chr11 - 68375252 68375250 68375252 AGACTTGGGGCCCAGGGGCCGTGTCTTCTATCACTGACCCCAGGGCACACGGAACTGGGGAGGGA AGACTTGGGGCCCAGGGGCCGTGTCTTCTATC__TGACCCCAGGGCACACGGAACTGGGGAGGGA AGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68375250..68375404 26863196 MeRIP-seq:(Medium) rs371487858 Functional Loss DEL dbSNP153 33..34 33 - - - 57343 RMVar_ID_57343 Human_SNP_ID_470845259 m1A Human chr11 + 68380985 68380985 68380985 TATGTGATCTAATTTGGAAACAGGGTCTTGGCAGATGTAATCAAGCGAGGATGAGGTCACCCTAG TATGTGATCTAATTTGGAAACAGGGTCTTGGCGGATGTAATCAAGCGAGGATGAGGTCACCCTAG A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68380981..68381065 26863196 MeRIP-seq:(Medium) rs643892 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6720 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_151178,RMVar_hsa_circ_151180 57344 RMVar_ID_57344 Human_SNP_ID_470845260 m1A Human chr11 + 68380985 68380985 68380985 TATGTGATCTAATTTGGAAACAGGGTCTTGGCAGATGTAATCAAGCGAGGATGAGGTCACCCTAG TATGTGATCTAATTTGGAAACAGGGTCTTGGCTGATGTAATCAAGCGAGGATGAGGTCACCCTAG A T LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68380981..68381065 26863196 MeRIP-seq:(Medium) rs643892 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6720 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_151178,RMVar_hsa_circ_151180 57345 RMVar_ID_57345 Human_SNP_ID_470847546 m1A Human chr11 + 68389946 68389946 68389946 TAAAATCGAGTGTGCCAACTTGGATGGGCAGGAGCGGCGTGTGCTGGTCAATGCCTCCCTCGGGT TAAAATCGAGTGTGCCAACTTGGATGGGCAGGGGCGGCGTGTGCTGGTCAATGCCTCCCTCGGGT A G LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:68389901..68390050 26863196 MeRIP-seq:(Medium) rs1211027012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773818,Human_RBP_ID_9275997,Human_RBP_ID_18974463,Human_RBP_ID_22433826,Human_RBP_ID_26768153 Human_Splice_Rec_1268518 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_66354,RMVar_hsa_circ_151178,RMVar_hsa_circ_300310,RMVar_hsa_circ_151180,RMVar_hsa_circ_363613,RMVar_hsa_circ_127861,RMVar_hsa_circ_151183,RMVar_hsa_circ_59948,RMVar_hsa_circ_151181,RMVar_hsa_circ_151182,RMVar_hsa_circ_75544,RMVar_hsa_circ_53985 57346 RMVar_ID_57346 Human_SNP_ID_470851197 m1A Human chr11 - 68403435 68403433 68403436 AATATAGGTCTGGATGGGCCAGGGCCACACCAACGAGAGCCAACCCGGACCCTGCCTGGGGCCTG AATATAGGTCTGGATGGGCCAGGGCCACACC___GAGAGCCAACCCGGACCCTGCCTGGGGCCTG CGTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68403432..68403512 26863196 MeRIP-seq:(Medium) rs778039810 Functional Loss DEL dbSNP153 32..34 33 - - - 57347 RMVar_ID_57347 Human_SNP_ID_470851199 m1A Human chr11 - 68403435 68403435 68403435 AATATAGGTCTGGATGGGCCAGGGCCACACCAACGAGAGCCAACCCGGACCCTGCCTGGGGCCTG AATATAGGTCTGGATGGGCCAGGGCCACACCAGCGAGAGCCAACCCGGACCCTGCCTGGGGCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68403432..68403512 26863196 MeRIP-seq:(Medium) rs1440377741 Functional Loss SNV dbSNP153 33..33 33 - - - 57348 RMVar_ID_57348 Human_SNP_ID_470851203 m1A Human chr11 - 68403447 68403447 68403447 CAGGACGGCAGAAATATAGGTCTGGATGGGCCAGGGCCACACCAACGAGAGCCAACCCGGACCCT CAGGACGGCAGAAATATAGGTCTGGATGGGCCTGGGCCACACCAACGAGAGCCAACCCGGACCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68403444..68403548 26863196 MeRIP-seq:(Medium) rs1392385815 Functional Loss SNV dbSNP153 33..33 33 - - - 57349 RMVar_ID_57349 Human_SNP_ID_470853271 m1A Human chr11 + 68410065 68410065 68410065 TGGGACCAACAGAATCGAAGTGGCGCGGCTGGACGGGCAGTTCCGGCAAGTCCTCGTGTGGAGGG TGGGACCAACAGAATCGAAGTGGCGCGGCTGGTCGGGCAGTTCCGGCAAGTCCTCGTGTGGAGGG A T LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:68409901..68410185 26863196 MeRIP-seq:(Medium) rs544505368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26320328 Human_Splice_Rec_1268525,Human_Splice_Rec_1268567,Human_Splice_Rec_1268593 RMVar_hsa_circ_38206,RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_124136,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_66354,RMVar_hsa_circ_151178,RMVar_hsa_circ_363613,RMVar_hsa_circ_127861,RMVar_hsa_circ_151183,RMVar_hsa_circ_151182,RMVar_hsa_circ_75544,RMVar_hsa_circ_53985,RMVar_hsa_circ_331344,RMVar_hsa_circ_351703,RMVar_hsa_circ_371280,RMVar_hsa_circ_346736,RMVar_hsa_circ_305187,RMVar_hsa_circ_151189,RMVar_hsa_circ_56990,RMVar_hsa_circ_122607,RMVar_hsa_circ_151186,RMVar_hsa_circ_151187,RMVar_hsa_circ_151188,RMVar_hsa_circ_358549,RMVar_hsa_circ_365063,RMVar_hsa_circ_101643,RMVar_hsa_circ_118796,RMVar_hsa_circ_87912,RMVar_hsa_circ_151191,RMVar_hsa_circ_151193,RMVar_hsa_circ_151194,RMVar_hsa_circ_151192,RMVar_hsa_circ_151190,RMVar_hsa_circ_22646,RMVar_hsa_circ_63454,RMVar_hsa_circ_80814,RMVar_hsa_circ_374807,RMVar_hsa_circ_48065,RMVar_hsa_circ_151196,RMVar_hsa_circ_151197 57350 RMVar_ID_57350 Human_SNP_ID_470853658 m1A Human chr11 + 68411506 68411506 68411506 TCGTGCGGGCCTTCATGGACGGGACCAACTGCATGACGCTGGTGGACAAGGTGGGCCGGGCCAAC TCGTGCGGGCCTTCATGGACGGGACCAACTGCGTGACGCTGGTGGACAAGGTGGGCCGGGCCAAC A G LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:68411388..68411561 26863196 MeRIP-seq:(Medium) rs775727748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402318,Human_RBP_ID_4176020 Human_Splice_Rec_1268526,Human_Splice_Rec_1268568,Human_Splice_Rec_1268594 RMVar_hsa_circ_38206,RMVar_hsa_circ_60233,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_124136,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_94107,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_66354,RMVar_hsa_circ_151178,RMVar_hsa_circ_363613,RMVar_hsa_circ_127861,RMVar_hsa_circ_151183,RMVar_hsa_circ_151182,RMVar_hsa_circ_75544,RMVar_hsa_circ_53985,RMVar_hsa_circ_331344,RMVar_hsa_circ_351703,RMVar_hsa_circ_371280,RMVar_hsa_circ_346736,RMVar_hsa_circ_305187,RMVar_hsa_circ_151189,RMVar_hsa_circ_56990,RMVar_hsa_circ_122607,RMVar_hsa_circ_151186,RMVar_hsa_circ_151187,RMVar_hsa_circ_151188,RMVar_hsa_circ_358549,RMVar_hsa_circ_365063,RMVar_hsa_circ_101643,RMVar_hsa_circ_118796,RMVar_hsa_circ_87912,RMVar_hsa_circ_151191,RMVar_hsa_circ_151193,RMVar_hsa_circ_151194,RMVar_hsa_circ_151192,RMVar_hsa_circ_151190,RMVar_hsa_circ_22646,RMVar_hsa_circ_63454,RMVar_hsa_circ_80814,RMVar_hsa_circ_374807,RMVar_hsa_circ_48065,RMVar_hsa_circ_151196,RMVar_hsa_circ_151197,RMVar_hsa_circ_151198,RMVar_hsa_circ_110988 57351 RMVar_ID_57351 Human_SNP_ID_470861381 m1A Human chr11 - 68438399 68438380 68438399 CAGAAAGAGGTGGCCAACATTAACCCCAACGGAATGGGCCCTCCTTGGGGGCAGACACCGTGCGC CAGAAAGAGGTGGCCAACATTAACCCCAACGG___________________CAGACACCGTGCGC GCCCCCAAGGAGGGCCCATT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68438398..68438475 26863196 MeRIP-seq:(Medium) rs1433944758 Functional Loss DEL dbSNP153 33..51 33 - - - 57352 RMVar_ID_57352 Human_SNP_ID_470861385 m1A Human chr11 - 68438399 68438399 68438399 CAGAAAGAGGTGGCCAACATTAACCCCAACGGAATGGGCCCTCCTTGGGGGCAGACACCGTGCGC CAGAAAGAGGTGGCCAACATTAACCCCAACGGGATGGGCCCTCCTTGGGGGCAGACACCGTGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68438398..68438475 26863196 MeRIP-seq:(Medium) rs755441813 Functional Loss SNV dbSNP153 33..33 33 - - - 57353 RMVar_ID_57353 Human_SNP_ID_470861882 m1A Human chr11 - 68439918 68439918 68439918 TCCCGCCCCGCCCCTCCCCGGCCCCGCCCCTCACCGGCGGGTACAGCGTGGCCTTCGTGCTGGAC TCCCGCCCCGCCCCTCCCCGGCCCCGCCCCTCCCCGGCGGGTACAGCGTGGCCTTCGTGCTGGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68439892..68439968 26863196 MeRIP-seq:(Medium) rs80358322 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_164 57354 RMVar_ID_57354 Human_SNP_ID_470863719 m1A Human chr11 + 68445924 68445917 68445925 GTGGTGACTTCTGTGTCAGGGCTTCAGCAGGGACGCAGAGCCCCTGAGTGTTCGGAACAAGGGCG GTGGTGACTTCTGTGTCAGGGCTTCA________GCAGAGCCCCTGAGTGTTCGGAACAAGGGCG AGCAGGGAC A LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68445921..68446065 26863196 MeRIP-seq:(Medium) rs1385833927 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_81769,RMVar_hsa_circ_151161 57355 RMVar_ID_57355 Human_SNP_ID_470870758 m1A Human chr11 - 68470394 68470394 68470394 CTCCAGCCACACTGGCCTCCGCTGCCCCTCCAACACAGCAGACATGCCTCCTTCTTAGCACCTTG CTCCAGCCACACTGGCCTCCGCTGCCCCTCCAGCACAGCAGACATGCCTCCTTCTTAGCACCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68470195..68470962 26863196 MeRIP-seq:(Medium) rs1208039102 Functional Loss SNV dbSNP153 33..33 33 - - - 57356 RMVar_ID_57356 Human_SNP_ID_470871140 m1A Human chr11 - 68471767 68471767 68471767 GCCTTCCCAAGAATGTGGCTCCAGCAAGGGTCACCTCTTCTGATTCATCATGTCATTCATCCTCT GCCTTCCCAAGAATGTGGCTCCAGCAAGGGTCGCCTCTTCTGATTCATCATGTCATTCATCCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:68471755..68472240 26863196 MeRIP-seq:(Medium) rs925118989 Functional Loss SNV dbSNP153 33..33 33 - - - 57357 RMVar_ID_57357 Human_SNP_ID_470891438 m1A Human chr11 + 68547346 68547346 68547346 CCCCCTGGGACTCGCAGAGGGTTTGGGAATAGATGACACGTGCGCATGGACAGAGGCAGAGGCAA CCCCCTGGGACTCGCAGAGGGTTTGGGAATAGGTGACACGTGCGCATGGACAGAGGCAGAGGCAA A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68547296..68547493 26863196 MeRIP-seq:(Medium) rs1251513249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11693023,Human_RBP_ID_18612001 RMVar_hsa_circ_151209,RMVar_hsa_circ_273670,RMVar_hsa_circ_324989,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838,RMVar_hsa_circ_365833,RMVar_hsa_circ_373954,RMVar_hsa_circ_338533,RMVar_hsa_circ_295394,RMVar_hsa_circ_306065,RMVar_hsa_circ_323265,RMVar_hsa_circ_107895,RMVar_hsa_circ_151211,RMVar_hsa_circ_151212,RMVar_hsa_circ_151210,RMVar_hsa_circ_32971,RMVar_hsa_circ_70039,RMVar_hsa_circ_341886,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_360207,RMVar_hsa_circ_74196,RMVar_hsa_circ_56180,RMVar_hsa_circ_56741,RMVar_hsa_circ_49309,RMVar_hsa_circ_315360,RMVar_hsa_circ_334306,RMVar_hsa_circ_348180,RMVar_hsa_circ_329940,RMVar_hsa_circ_322361,RMVar_hsa_circ_298364,RMVar_hsa_circ_313658,RMVar_hsa_circ_289577,RMVar_hsa_circ_27823,RMVar_hsa_circ_64334,RMVar_hsa_circ_52327,RMVar_hsa_circ_151219,RMVar_hsa_circ_151221,RMVar_hsa_circ_151222,RMVar_hsa_circ_151223,RMVar_hsa_circ_151220,RMVar_hsa_circ_151225,RMVar_hsa_circ_16302,RMVar_hsa_circ_281117,RMVar_hsa_circ_286068,RMVar_hsa_circ_306222,RMVar_hsa_circ_318783,RMVar_hsa_circ_282134,RMVar_hsa_circ_50286,RMVar_hsa_circ_64476,RMVar_hsa_circ_19663,RMVar_hsa_circ_151227,RMVar_hsa_circ_151229,RMVar_hsa_circ_151230,RMVar_hsa_circ_151228,RMVar_hsa_circ_151226,RMVar_hsa_circ_97759,RMVar_hsa_circ_300116,RMVar_hsa_circ_323847,RMVar_hsa_circ_353286,RMVar_hsa_circ_151231,RMVar_hsa_circ_352622,RMVar_hsa_circ_316142,RMVar_hsa_circ_281211,RMVar_hsa_circ_151233,RMVar_hsa_circ_151234,RMVar_hsa_circ_151232 57358 RMVar_ID_57358 Human_SNP_ID_470900021 m1A Human chr11 + 68580425 68580425 68580425 TGGGGCAAGAGCTAGGAGGAGGGAGACTGGGGAACTGCCAGCTGTGACATTAGTCCAGGTGAGGG TGGGGCAAGAGCTAGGAGGAGGGAGACTGGGGCACTGCCAGCTGTGACATTAGTCCAGGTGAGGG A C PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68580376..68580629 26863196 MeRIP-seq:(Medium) rs1183028927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5139397,Human_RBP_ID_6089953,Human_RBP_ID_11694246,Human_RBP_ID_24362931 RMVar_hsa_circ_9301,RMVar_hsa_circ_373954,RMVar_hsa_circ_107895,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_74196,RMVar_hsa_circ_329940,RMVar_hsa_circ_27823,RMVar_hsa_circ_52327,RMVar_hsa_circ_16302,RMVar_hsa_circ_64476,RMVar_hsa_circ_151230,RMVar_hsa_circ_97759,RMVar_hsa_circ_300116,RMVar_hsa_circ_151234,RMVar_hsa_circ_349824,RMVar_hsa_circ_296401,RMVar_hsa_circ_151236,RMVar_hsa_circ_151235,RMVar_hsa_circ_84137,RMVar_hsa_circ_341477,RMVar_hsa_circ_151243,RMVar_hsa_circ_344130,RMVar_hsa_circ_336680,RMVar_hsa_circ_63560,RMVar_hsa_circ_275013,RMVar_hsa_circ_151244,RMVar_hsa_circ_151245,RMVar_hsa_circ_354165,RMVar_hsa_circ_288113,RMVar_hsa_circ_151248,RMVar_hsa_circ_151249,RMVar_hsa_circ_47787,RMVar_hsa_circ_321006,RMVar_hsa_circ_360142,RMVar_hsa_circ_57535,RMVar_hsa_circ_278579,RMVar_hsa_circ_321720,RMVar_hsa_circ_286808,RMVar_hsa_circ_151251,RMVar_hsa_circ_151253,RMVar_hsa_circ_151252,RMVar_hsa_circ_68037,RMVar_hsa_circ_279641,RMVar_hsa_circ_151250,RMVar_hsa_circ_336249,RMVar_hsa_circ_284914,RMVar_hsa_circ_273918,RMVar_hsa_circ_151257,RMVar_hsa_circ_151258,RMVar_hsa_circ_151256,RMVar_hsa_circ_333208,RMVar_hsa_circ_348775,RMVar_hsa_circ_359879,RMVar_hsa_circ_91518,RMVar_hsa_circ_47055,RMVar_hsa_circ_151260,RMVar_hsa_circ_151261 57359 RMVar_ID_57359 Human_SNP_ID_470928149 m1A Human chr11 + 68684676 68684676 68684676 GACCCGGCCCGACGCCCGGACCTGCCGCCCAGACCCGCCACCGCACCCGGACCCCGACGCTCCGA GACCCGGCCCGACGCCCGGACCTGCCGCCCAGCCCCGCCACCGCACCCGGACCCCGACGCTCCGA A C GAL Ensembl:ENSG00000069482 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68684488..68684786 26863196 MeRIP-seq:(Medium) rs1013768928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402399,Human_RBP_ID_4185224 Human_Splice_Rec_1269159 57360 RMVar_ID_57360 Human_SNP_ID_470928238 m1A Human chr11 - 68684908 68684908 68684908 GCGCTGCCTCGGGCCATCTGGAAGGGAAGGACAGGGCGGGCGGGTCGGAACCCGGAGTGGGCTGC GCGCTGCCTCGGGCCATCTGGAAGGGAAGGACTGGGCGGGCGGGTCGGAACCCGGAGTGGGCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68684901..68685025 26863196 MeRIP-seq:(Medium) rs1264339808 Functional Loss SNV dbSNP153 33..33 33 - - - 57361 RMVar_ID_57361 Human_SNP_ID_470928478 m1A Human chr11 - 68685579 68685579 68685579 GCCTCGTTTTTCCTTGGCCTTGAAGGGAGAAAAGGGGATCAGATGCCAGGGCTGTGCCTGGAGCC GCCTCGTTTTTCCTTGGCCTTGAAGGGAGAAAGGGGGATCAGATGCCAGGGCTGTGCCTGGAGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68685576..68685650 26863196 MeRIP-seq:(Medium) rs1021754734 Functional Loss SNV dbSNP153 33..33 33 - - - 57362 RMVar_ID_57362 Human_SNP_ID_470929421 m1A Human chr11 + 68688924 68688924 68688924 AATCATTGAGTTTCTGTCTTTCTTGCATCTCAAAGGTATGTGAAATATCATCAACTTAACATTCA AATCATTGAGTTTCTGTCTTTCTTGCATCTCAGAGGTATGTGAAATATCATCAACTTAACATTCA A G GAL Ensembl:ENSG00000069482 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68688899..68688974 26863196 MeRIP-seq:(Medium) rs749326051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2279187,Human_RBP_ID_17350285,Human_RBP_ID_22753723,Human_RBP_ID_26803930 Human_Splice_Rec_1269166,Human_Splice_Rec_1269167 RMVar_hsa_circ_96272,RMVar_hsa_circ_80026,RMVar_hsa_circ_103899,RMVar_hsa_circ_151276,RMVar_hsa_circ_151277,RMVar_hsa_circ_102705,RMVar_hsa_circ_151278,RMVar_hsa_circ_151280 57363 RMVar_ID_57363 Human_SNP_ID_470943901 m1A Human chr11 - 68751396 68751396 68751396 CGGCCCCAGGTGCGTCCCTCCGAGGAGGAATGACGGGGCGGTCCCCGGGCTGGGCCTCGGCTCTG CGGCCCCAGGTGCGTCCCTCCGAGGAGGAATGGCGGGGCGGTCCCCGGGCTGGGCCTCGGCTCTG T C TESMIN Ensembl:ENSG00000132749 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68751387..68751497 26863196 MeRIP-seq:(Medium) rs1253444807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19054116 57364 RMVar_ID_57364 Human_SNP_ID_470947246 m1A Human chr11 - 68763622 68763622 68763622 CTTCACCCAGAAAACAGGAGCTTTTGGAAGAGACCTTCCCTGTGCATCTGCCAGCCCACCCGAGG CTTCACCCAGAAAACAGGAGCTTTTGGAAGAGCCCTTCCCTGTGCATCTGCCAGCCCACCCGAGG T G CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68763601..68763727 26863196 MeRIP-seq:(Medium) rs1208729886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124168,RMVar_hsa_circ_40006,RMVar_hsa_circ_94639,RMVar_hsa_circ_151283,RMVar_hsa_circ_349165,RMVar_hsa_circ_314725,RMVar_hsa_circ_82438,RMVar_hsa_circ_151287,RMVar_hsa_circ_151288,RMVar_hsa_circ_151289,RMVar_hsa_circ_92877,RMVar_hsa_circ_151291,RMVar_hsa_circ_102049,RMVar_hsa_circ_151292,RMVar_hsa_circ_151293,RMVar_hsa_circ_322934 57365 RMVar_ID_57365 Human_SNP_ID_470967030 m1A Human chr11 + 68841810 68841807 68841810 GTCAGCTACGGAGGTGCGGCAGCGGCAGCGGCAGCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC GTCAGCTACGGAGGTGCGGCAGCGGCAGCG___GCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC GGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:68841704..68841900;chr11:68841733..68841894;chr11:68841732..68841876 26863196 MeRIP-seq:(Medium) rs903806235 Functional Loss DEL dbSNP153 31..33 33 - - - 57366 RMVar_ID_57366 Human_SNP_ID_470967033 m1A Human chr11 + 68841810 68841810 68841810 GTCAGCTACGGAGGTGCGGCAGCGGCAGCGGCAGCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC GTCAGCTACGGAGGTGCGGCAGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:68841704..68841900;chr11:68841733..68841894;chr11:68841732..68841876 26863196 MeRIP-seq:(Medium) rs1000188907 Functional Loss SNV dbSNP153 33..33 33 - - - 57367 RMVar_ID_57367 Human_SNP_ID_470973139 m1A Human chr11 - 68865199 68865199 68865199 GTCTTTGCAAGGGGGAAGGGCTTGCCCGAGTCAAGGTGGAGCAGTGAGGCCCCTGCCTATTTTCA GTCTTTGCAAGGGGGAAGGGCTTGCCCGAGTCGAGGTGGAGCAGTGAGGCCCCTGCCTATTTTCA T C HSALNG0085265 RNACentral:URS0000E9BB11 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68865196..68865312 32194978 MeRIP-seq:(Medium) rs1378334838 Functional Loss SNV dbSNP153 33..33 33 - - - 57368 RMVar_ID_57368 Human_SNP_ID_470980248 m1A Human chr11 + 68892138 68892135 68892138 GGGAGCGAGGTGGGTTCACGCGCGGAGGGTGGAGGAGAAGGGGAGCGAGGTGGGTTCACGCGCGG GGGAGCGAGGTGGGTTCACGCGCGGAGGGT___GGAGAAGGGGAGCGAGGTGGGTTCACGCGCGG TGGA T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:68892018..68892212 26863196 MeRIP-seq:(Medium) rs1327820842 Functional Loss DEL dbSNP153 31..33 33 - - - 57369 RMVar_ID_57369 Human_SNP_ID_470980250 m1A Human chr11 + 68892138 68892138 68892138 GGGAGCGAGGTGGGTTCACGCGCGGAGGGTGGAGGAGAAGGGGAGCGAGGTGGGTTCACGCGCGG GGGAGCGAGGTGGGTTCACGCGCGGAGGGTGGGGGAGAAGGGGAGCGAGGTGGGTTCACGCGCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:68892018..68892212 26863196 MeRIP-seq:(Medium) rs1240784403 Functional Loss SNV dbSNP153 33..33 33 - - - 57370 RMVar_ID_57370 Human_SNP_ID_470980396 m1A Human chr11 + 68892700 68892700 68892700 AGCGAGGTGGGGTCACGCGTGGAGCGTGGAGGAGAAGGGGAGCGAGGCTGGACCCTCTGGGTGCT AGCGAGGTGGGGTCACGCGTGGAGCGTGGAGGGGAAGGGGAGCGAGGCTGGACCCTCTGGGTGCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:68892666..68892826 26863196 MeRIP-seq:(Medium) rs1444346558 Functional Loss SNV dbSNP153 33..33 33 - - - 57371 RMVar_ID_57371 Human_SNP_ID_470981849 m1A Human chr11 - 68897932 68897932 68897932 TCTGCCAGACCCAGTTGAGGAGACCAGACACCATGCAGGTAAGACCTCCCTGGGAGACAGAAGCT TCTGCCAGACCCAGTTGAGGAGACCAGACACCGTGCAGGTAAGACCTCCCTGGGAGACAGAAGCT T C MRPL21 Ensembl:ENSG00000197345 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68897926..68898025 32194978 MeRIP-seq:(Medium) rs1177004716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865361,Human_RBP_ID_9322267,Human_RBP_ID_9362664,Human_RBP_ID_18974483,Human_RBP_ID_22434695,Human_RBP_ID_22792098 Human_Splice_Rec_1269404,Human_Splice_Rec_1269405,Human_Splice_Rec_1269416,Human_Splice_Rec_1269417,Human_Splice_Rec_1269428,Human_Splice_Rec_1269429,Human_Splice_Rec_1269438,Human_Splice_Rec_1269439,Human_Splice_Rec_1269450,Human_Splice_Rec_1269451,Human_Splice_Rec_1269458,Human_Splice_Rec_1269459,Human_Splice_Rec_1269468,Human_Splice_Rec_1269469,Human_Splice_Rec_1269478 RMVar_hsa_circ_310704,RMVar_hsa_circ_84217,RMVar_hsa_circ_151321,RMVar_hsa_circ_68010,RMVar_hsa_circ_313711,RMVar_hsa_circ_111187,RMVar_hsa_circ_151322,RMVar_hsa_circ_151323 57372 RMVar_ID_57372 Human_SNP_ID_470981883 m1A Human chr11 - 68898014 68898014 68898014 CTTGTGACATTTGTCTACGAAATGTGTTTTACAGATATGTTCCTAAAACATCCCTGAGTTCACCA CTTGTGACATTTGTCTACGAAATGTGTTTTACTGATATGTTCCTAAAACATCCCTGAGTTCACCA T A MRPL21 Ensembl:ENSG00000197345 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68897976..68898025 32194978 MeRIP-seq:(Medium) rs111451120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2279420,Human_RBP_ID_4176240,Human_RBP_ID_17234173 Human_Splice_Rec_1269405,Human_Splice_Rec_1269417,Human_Splice_Rec_1269429,Human_Splice_Rec_1269439,Human_Splice_Rec_1269451,Human_Splice_Rec_1269459,Human_Splice_Rec_1269469 RMVar_hsa_circ_68010,RMVar_hsa_circ_111187,RMVar_hsa_circ_151323 57373 RMVar_ID_57373 Human_SNP_ID_470981884 m1A Human chr11 - 68898014 68898014 68898014 CTTGTGACATTTGTCTACGAAATGTGTTTTACAGATATGTTCCTAAAACATCCCTGAGTTCACCA CTTGTGACATTTGTCTACGAAATGTGTTTTACGGATATGTTCCTAAAACATCCCTGAGTTCACCA T C MRPL21 Ensembl:ENSG00000197345 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68897976..68898025 32194978 MeRIP-seq:(Medium) rs111451120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2279420,Human_RBP_ID_4176240,Human_RBP_ID_17234173 Human_Splice_Rec_1269405,Human_Splice_Rec_1269417,Human_Splice_Rec_1269429,Human_Splice_Rec_1269439,Human_Splice_Rec_1269451,Human_Splice_Rec_1269459,Human_Splice_Rec_1269469 RMVar_hsa_circ_68010,RMVar_hsa_circ_111187,RMVar_hsa_circ_151323 57374 RMVar_ID_57374 Human_SNP_ID_470982507 m1A Human chr11 + 68900529 68900529 68900529 GTTCTACAAATGAAAGGAAAAGAGGCACCAAAACCCACATTTTGATATTACCCTGGTAGATATGA GTTCTACAAATGAAAGGAAAAGAGGCACCAAAGCCCACATTTTGATATTACCCTGGTAGATATGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:68900526..68900625;chr11:68900526..68900600 32194978 MeRIP-seq:(Medium) rs373501945 Functional Loss SNV dbSNP153 33..33 33 - - - 57375 RMVar_ID_57375 Human_SNP_ID_470983301 m1A Human chr11 + 68903773 68903773 68903773 GTCTCAGGATGCTGTGGCTGCACGCGGACGCCAGCCGCCCTAAGGTGACCGTCAGGGAAGATGCT GTCTCAGGATGCTGTGGCTGCACGCGGACGCCGGCCGCCCTAAGGTGACCGTCAGGGAAGATGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68903691..68903796 26863196 MeRIP-seq:(Medium) rs1266013993 Functional Loss SNV dbSNP153 33..33 33 - - - 57376 RMVar_ID_57376 Human_SNP_ID_470983414 m1A Human chr11 + 68903930 68903930 68903930 CGGCCCGGCGCAGAAGCGGGACGTCGGCTTCTAGGGGCCCAGGCCGGCGGCGGCGATGGCCTCGG CGGCCCGGCGCAGAAGCGGGACGTCGGCTTCTGGGGGCCCAGGCCGGCGGCGGCGATGGCCTCGG A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68903883..68904033 26863196 MeRIP-seq:(Medium) rs1347732611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4176251 57377 RMVar_ID_57377 Human_SNP_ID_470983420 m1A Human chr11 + 68903938 68903938 68903938 CGCAGAAGCGGGACGTCGGCTTCTAGGGGCCCAGGCCGGCGGCGGCGATGGCCTCGGCAGCTGTG CGCAGAAGCGGGACGTCGGCTTCTAGGGGCCCGGGCCGGCGGCGGCGATGGCCTCGGCAGCTGTG A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68903890..68904030 26863196 MeRIP-seq:(Medium) rs759682770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185233 57378 RMVar_ID_57378 Human_SNP_ID_470983986 m1A Human chr11 - 68906032 68906032 68906032 AAGACACCCGGTATTGATGCTTCAGGATTTTTACTAGTTTCTACTTCCACCCACCCAGGAAAAGT AAGACACCCGGTATTGATGCTTCAGGATTTTTGCTAGTTTCTACTTCCACCCACCCAGGAAAAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68906030..68906147 26863196 MeRIP-seq:(Medium) rs1388590019 Functional Loss SNV dbSNP153 33..33 33 - - - 57379 RMVar_ID_57379 Human_SNP_ID_470984060 m1A Human chr11 - 68906170 68906167 68906170 ACCCGTATCGCCTGGGCTCAAAGGTGACCAGCAGCCGTCCGTACAGCCCAGTGCGCTGGCTGGAT ACCCGTATCGCCTGGGCTCAAAGGTGACCAGC___CGTCCGTACAGCCCAGTGCGCTGGCTGGAT GGCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68906120..68906220 32194978 MeRIP-seq:(Medium) rs1359229269 Functional Loss DEL dbSNP153 33..35 33 - - - 57380 RMVar_ID_57380 Human_SNP_ID_470990571 m1A Human chr11 - 68930465 68930465 68930465 TTCCAACATCTTCCTCCCAAAGCTCACTCTCAATTACTATTTTTGACACCTCTCTCTACATACCC TTCCAACATCTTCCTCCCAAAGCTCACTCTCAGTTACTATTTTTGACACCTCTCTCTACATACCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:68930359..68930724 26863196 MeRIP-seq:(Medium) rs537149910 Functional Loss SNV dbSNP153 33..33 33 - - - 57381 RMVar_ID_57381 Human_SNP_ID_470990919 m1A Human chr11 - 68931894 68931894 68931894 AACCATCCTACTCTCTGCAGGGAACGCCACCCAACGTCTTCCCCCGAAACCATCCTACTCCCTCC AACCATCCTACTCTCTGCAGGGAACGCCACCCGACGTCTTCCCCCGAAACCATCCTACTCCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68931843..68932301 26863196 MeRIP-seq:(Medium) rs978198214 Functional Loss SNV dbSNP153 33..33 33 - - - 57382 RMVar_ID_57382 Human_SNP_ID_470991015 m1A Human chr11 - 68932127 68932127 68932127 AACCATTCTACTCTCTCCAGGGAATGCCACCCAACGTCTTCCCCCGAAACCATCCTACTCTCTCC AACCATTCTACTCTCTCCAGGGAATGCCACCCCACGTCTTCCCCCGAAACCATCCTACTCTCTCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:68931905..68932197 26863196 MeRIP-seq:(Medium) rs1405839490 Functional Loss SNV dbSNP153 33..33 33 - - - 57383 RMVar_ID_57383 Human_SNP_ID_470993462 m1A Human chr11 - 68939955 68939955 68939955 TAAGGGGAAGGGACGTGCATTTCCCAAGCCCCACCTGCACGAGCACTGTTGTCCCCCAGGTGCTT TAAGGGGAAGGGACGTGCATTTCCCAAGCCCCCCCTGCACGAGCACTGTTGTCCCCCAGGTGCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68939905..68940204 32194978 MeRIP-seq:(Medium) rs971315347 Functional Loss SNV dbSNP153 33..33 33 - - - 57384 RMVar_ID_57384 Human_SNP_ID_471088136 m1A Human chr11 + 69295778 69295778 69295778 TTGCTGCTGGAGCTGGTGACCGGGAGAGAAACAAGGGAGACAAGGGTGCCCAGACAGGTGCGGGG TTGCTGCTGGAGCTGGTGACCGGGAGAGAAACGAGGGAGACAAGGGTGCCCAGACAGGTGCGGGG A G MYEOV Ensembl:ENSG00000172927 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:69295774..69295905 26863196 MeRIP-seq:(Medium) rs1305868490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709224 RMVar_hsa_circ_151344,RMVar_hsa_circ_98677,RMVar_hsa_circ_88443,RMVar_hsa_circ_151345 57385 RMVar_ID_57385 Human_SNP_ID_471179187 m1A Human chr11 + 69641263 69641263 69641263 CGCGGGGCAGCAGAAGCGAGAGCCGAGCGCGGACCCAGCCAGGACCCACAGCCCTCCCCAGCTGC CGCGGGGCAGCAGAAGCGAGAGCCGAGCGCGGTCCCAGCCAGGACCCACAGCCCTCCCCAGCTGC A T CCND1 Ensembl:ENSG00000110092 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:69641212..69641419;chr11:69641212..69641374 26863196 MeRIP-seq:(Medium) rs567650296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27803746 Human_miRNA_ID_2331970,Human_miRNA_ID_2965055 RMVar_hsa_circ_84086,RMVar_hsa_circ_151346 57386 RMVar_ID_57386 Human_SNP_ID_471179481 m1A Human chr11 + 69642094 69642094 69642094 TAAGGGCCGCGCGGCTGCCGGGAGCCCGCGGGAGGGGCGCAGGGACGCGGCATGGGTAGTTTTGG TAAGGGCCGCGCGGCTGCCGGGAGCCCGCGGGGGGGGCGCAGGGACGCGGCATGGGTAGTTTTGG A G CCND1 Ensembl:ENSG00000110092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:69642086..69642256 26863196 MeRIP-seq:(Medium) rs1047557668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84086,RMVar_hsa_circ_151346 57387 RMVar_ID_57387 Human_SNP_ID_471182353 m1A Human chr11 + 69651194 69651194 69651194 GTCAAGCCTGCGCCAGGCCCAGCAGAACATGGACCCCAAGGCCGCCGAGGAGGAGGAAGAGGAGG GTCAAGCCTGCGCCAGGCCCAGCAGAACATGGGCCCCAAGGCCGCCGAGGAGGAGGAAGAGGAGG A G CCND1 Ensembl:ENSG00000110092 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:69651144..69651325 26863196 MeRIP-seq:(Medium) rs377271027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6090490 Human_Splice_Rec_1269984,Human_Splice_Rec_1269996 Human_miRNA_ID_2017853 RMVar_hsa_circ_151347,RMVar_hsa_circ_86573 57388 RMVar_ID_57388 Human_SNP_ID_120501142 m1A Human chr3 - 3126992 3126992 3126992 ACTCTGCCCCTCTGAGCGGCGCGCGCCCGCTTACCGGCCCCGCTGTTGCCGCAGCCGCCACCGCC ACTCTGCCCCTCTGAGCGGCGCGCGCCCGCTTGCCGGCCCCGCTGTTGCCGCAGCCGCCACCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:3126965..3127053;chr3:3126977..3127106;chr3:3126973..3127105 26863196 MeRIP-seq:(Medium) rs1297006000 Functional Loss SNV dbSNP153 33..33 33 - - - 57389 RMVar_ID_57389 Human_SNP_ID_120518027 m1A Human chr3 - 3179653 3179653 3179653 GGCCGGCGAAGGAGATCAGCAGGACGCTGCGCACAACATGGGCAACCACCTGCCGCTCCTGCCTG GGCCGGCGAAGGAGATCAGCAGGACGCTGCGCCCAACATGGGCAACCACCTGCCGCTCCTGCCTG T G CRBN Ensembl:ENSG00000113851 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:3179572..3179655 26863196 MeRIP-seq:(Medium) rs1392453549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7186892,Human_RBP_ID_18446483,Human_RBP_ID_26346393,Human_RBP_ID_27821804 Human_Splice_Rec_385049,Human_Splice_Rec_385071,Human_Splice_Rec_385087,Human_Splice_Rec_385105,Human_Splice_Rec_385125,Human_Splice_Rec_385171,Human_Splice_Rec_385179,Human_Splice_Rec_385191 57390 RMVar_ID_57390 Human_SNP_ID_120518048 m1A Human chr3 - 3179665 3179663 3179666 GTAAACAGACATGGCCGGCGAAGGAGATCAGCAGGACGCTGCGCACAACATGGGCAACCACCTGC GTAAACAGACATGGCCGGCGAAGGAGATCAG___GACGCTGCGCACAACATGGGCAACCACCTGC CCTG C CRBN Ensembl:ENSG00000113851 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:3179591..3179700 26863196 MeRIP-seq:(Medium) rs1559261370 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_7186892,Human_RBP_ID_26347664,Human_RBP_ID_27822895 Human_Splice_Rec_385049,Human_Splice_Rec_385071,Human_Splice_Rec_385087,Human_Splice_Rec_385105,Human_Splice_Rec_385125,Human_Splice_Rec_385171,Human_Splice_Rec_385179,Human_Splice_Rec_385191 57391 RMVar_ID_57391 Human_SNP_ID_120518049 m1A Human chr3 - 3179665 3179665 3179665 GTAAACAGACATGGCCGGCGAAGGAGATCAGCAGGACGCTGCGCACAACATGGGCAACCACCTGC GTAAACAGACATGGCCGGCGAAGGAGATCAGCGGGACGCTGCGCACAACATGGGCAACCACCTGC T C CRBN Ensembl:ENSG00000113851 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:3179591..3179700 26863196 MeRIP-seq:(Medium) rs147395766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7186892,Human_RBP_ID_26347664,Human_RBP_ID_27822895 Human_Splice_Rec_385049,Human_Splice_Rec_385071,Human_Splice_Rec_385087,Human_Splice_Rec_385105,Human_Splice_Rec_385125,Human_Splice_Rec_385171,Human_Splice_Rec_385179,Human_Splice_Rec_385191 57392 RMVar_ID_57392 Human_SNP_ID_120518050 m1A Human chr3 - 3179665 3179665 3179665 GTAAACAGACATGGCCGGCGAAGGAGATCAGCAGGACGCTGCGCACAACATGGGCAACCACCTGC GTAAACAGACATGGCCGGCGAAGGAGATCAGCCGGACGCTGCGCACAACATGGGCAACCACCTGC T G CRBN Ensembl:ENSG00000113851 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:3179591..3179700 26863196 MeRIP-seq:(Medium) rs147395766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7186892,Human_RBP_ID_26347664,Human_RBP_ID_27822895 Human_Splice_Rec_385049,Human_Splice_Rec_385071,Human_Splice_Rec_385087,Human_Splice_Rec_385105,Human_Splice_Rec_385125,Human_Splice_Rec_385171,Human_Splice_Rec_385179,Human_Splice_Rec_385191 57393 RMVar_ID_57393 Human_SNP_ID_120848505 m1A Human chr3 + 4303426 4303426 4303426 GACACGGCCTTGTGGGATGGCGGAGTTTAAGGAGAAGCCTGAGGCCCCGACTGAGCAGCTGGATG GACACGGCCTTGTGGGATGGCGGAGTTTAAGGGGAAGCCTGAGGCCCCGACTGAGCAGCTGGATG A G SETMAR Ensembl:ENSG00000170364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:4303375..4303502;chr3:4303357..4303565;chr3:4303351..4303506 26863196 MeRIP-seq:(Medium) rs1032777383 Functional Loss SNV dbSNP153 33..33 33 - - - 57394 RMVar_ID_57394 Human_SNP_ID_120881282 m1A Human chr3 + 4420104 4420102 4420104 AATAGTAGAGTCAGGCCCTTCTGGGTGTCTCCAGTTAGCGCCTTTCACAGGTAACCACCAGGGAG AATAGTAGAGTCAGGCCCTTCTGGGTGTCTC__GTTAGCGCCTTTCACAGGTAACCACCAGGGAG CCA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:4418124..4449274 32194978 MeRIP-seq:(Medium) rs1262799846 Functional Loss DEL dbSNP153 32..33 33 - - - 57395 RMVar_ID_57395 Human_SNP_ID_120894559 m1A Human chr3 - 4467006 4467006 4467006 TACTCGCGGGAGGCTAACGCTCCGGGCCCCGTACCCGGAGAGCGGCAACTCGCGCACTCAAAGGT TACTCGCGGGAGGCTAACGCTCCGGGCCCCGTGCCCGGAGAGCGGCAACTCGCGCACTCAAAGGT T C SUMF1 Ensembl:ENSG00000144455 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:4466982..4467082 32194978 MeRIP-seq:(Medium) rs766851609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150224 Human_Splice_Rec_385229,Human_Splice_Rec_385259,Human_Splice_Rec_385275,Human_Splice_Rec_385289,Human_Splice_Rec_385297 57396 RMVar_ID_57396 Human_SNP_ID_120894560 m1A Human chr3 - 4467006 4467006 4467006 TACTCGCGGGAGGCTAACGCTCCGGGCCCCGTACCCGGAGAGCGGCAACTCGCGCACTCAAAGGT TACTCGCGGGAGGCTAACGCTCCGGGCCCCGTCCCCGGAGAGCGGCAACTCGCGCACTCAAAGGT T G SUMF1 Ensembl:ENSG00000144455 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:4466982..4467082 32194978 MeRIP-seq:(Medium) rs766851609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150224 Human_Splice_Rec_385229,Human_Splice_Rec_385259,Human_Splice_Rec_385275,Human_Splice_Rec_385289,Human_Splice_Rec_385297 57397 RMVar_ID_57397 Human_SNP_ID_120894685 m1A Human chr3 + 4467178 4467178 4467178 TCCCTGCCGCTCCACACAGCAGCGAGAGCAGCAGCAGCAAGAGGACGAGACCCAGCTCAGGGCAA TCCCTGCCGCTCCACACAGCAGCGAGAGCAGCTGCAGCAAGAGGACGAGACCCAGCTCAGGGCAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:4467129..4467197 26863196 MeRIP-seq:(Medium) rs775879406 Functional Loss SNV dbSNP153 33..33 33 - - - 57398 RMVar_ID_57398 Human_SNP_ID_120918358 m1A Human chr3 - 4554461 4554461 4554461 TGGCACATAGCCAGCATCAAAAACAAGGATTCAATTGATTCATGCCCACAAAAAACATTTACTAA TGGCACATAGCCAGCATCAAAAACAAGGATTCCATTGATTCATGCCCACAAAAAACATTTACTAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:4554458..4554634 26863196 MeRIP-seq:(Medium) rs144624797 Functional Loss SNV dbSNP153 33..33 33 - - - 57399 RMVar_ID_57399 Human_SNP_ID_120918359 m1A Human chr3 + 4554464 4554464 4554464 GTAAATGTTTTTTGTGGGCATGAATCAATTGAATCCTTGTTTTTGATGCTGGCTATGTGCCAGGC GTAAATGTTTTTTGTGGGCATGAATCAATTGAGTCCTTGTTTTTGATGCTGGCTATGTGCCAGGC A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:4554459..4554636 26863196 MeRIP-seq:(Medium) rs1479905936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24004557 RMVar_hsa_circ_86176,RMVar_hsa_circ_97271,RMVar_hsa_circ_117644,RMVar_hsa_circ_215503,RMVar_hsa_circ_99350,RMVar_hsa_circ_215505,RMVar_hsa_circ_215506,RMVar_hsa_circ_215507 57400 RMVar_ID_57400 Human_SNP_ID_120918376 m1A Human chr3 + 4554534 4554534 4554534 TGTAGGTGCTGGGGACCTACGGTGGTGAGCTCACTGGTGGGTTGGGCTGGAGAGAAAGGGGTCGT TGTAGGTGCTGGGGACCTACGGTGGTGAGCTCGCTGGTGGGTTGGGCTGGAGAGAAAGGGGTCGT A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:4554431..4554646 26863196 MeRIP-seq:(Medium) rs1209154795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86176,RMVar_hsa_circ_97271,RMVar_hsa_circ_117644,RMVar_hsa_circ_215503,RMVar_hsa_circ_99350,RMVar_hsa_circ_215505,RMVar_hsa_circ_215506,RMVar_hsa_circ_215507 57401 RMVar_ID_57401 Human_SNP_ID_120926500 m1A Human chr3 + 4584864 4584864 4584864 AGGGACTGTCCCCATCATAGGAGATGAAGCAAATGAAGAGACAAAATGAAGCAAATGAAGAGGCA AGGGACTGTCCCCATCATAGGAGATGAAGCAATTGAAGAGACAAAATGAAGCAAATGAAGAGGCA A T ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:4584861..4584985 26863196 MeRIP-seq:(Medium) rs550572519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86176,RMVar_hsa_circ_97271,RMVar_hsa_circ_117644,RMVar_hsa_circ_215503,RMVar_hsa_circ_99350,RMVar_hsa_circ_215505,RMVar_hsa_circ_215506,RMVar_hsa_circ_215507 57402 RMVar_ID_57402 Human_SNP_ID_120939814 m1A Human chr3 - 4629712 4629712 4629712 CTCCCACAGCTTTGTGTGGTTTGTCCTGTAATATAGTACTTATCACTGCCTCTTTATTCTTTGAT CTCCCACAGCTTTGTGTGGTTTGTCCTGTAATGTAGTACTTATCACTGCCTCTTTATTCTTTGAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:4629710..4629884 26863196 MeRIP-seq:(Medium) rs770926730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1137958 57403 RMVar_ID_57403 Human_SNP_ID_120944417 m1A Human chr3 + 4646344 4646344 4646344 TAAGGAAGACTTCCTGAAGGAGATAGCATCTGATCTGGTACCTGCAGGATGATTTGTATTTCAGA TAAGGAAGACTTCCTGAAGGAGATAGCATCTGGTCTGGTACCTGCAGGATGATTTGTATTTCAGA A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:4646294..4646364 26863196 MeRIP-seq:(Medium) rs1431870498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9570,RMVar_hsa_circ_86176,RMVar_hsa_circ_97271,RMVar_hsa_circ_117644,RMVar_hsa_circ_215503,RMVar_hsa_circ_215505,RMVar_hsa_circ_215506,RMVar_hsa_circ_95604,RMVar_hsa_circ_215510,RMVar_hsa_circ_33939,RMVar_hsa_circ_266234,RMVar_hsa_circ_12198,RMVar_hsa_circ_127064,RMVar_hsa_circ_49388,RMVar_hsa_circ_215512 57404 RMVar_ID_57404 Human_SNP_ID_120955066 m1A Human chr3 - 4683432 4683432 4683432 ATGCATCGTCAAGTGGAGCAGGACACGGAGAAAGGTTCTGCCGCCGTGGTCATCCAAGTCCAGTG ATGCATCGTCAAGTGGAGCAGGACACGGAGAAGGGTTCTGCCGCCGTGGTCATCCAAGTCCAGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:4683376..4683568 26863196 MeRIP-seq:(Medium) rs762525136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215525 57405 RMVar_ID_57405 Human_SNP_ID_120955072 m1A Human chr3 + 4683469 4683469 4683469 CCGTGTCCTGCTCCACTTGACGATGCATGACTACCCACCCCTGGTGTCAGGGGCCCTGCAGCTCC CCGTGTCCTGCTCCACTTGACGATGCATGACTGCCCACCCCTGGTGTCAGGGGCCCTGCAGCTCC A G ITPR1 Ensembl:ENSG00000150995 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:4683451..4683475 26863196 MeRIP-seq:(Medium) rs1382664089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9141142,Human_RBP_ID_9302695,Human_RBP_ID_9394541 Human_Splice_Rec_385427,Human_Splice_Rec_385537,Human_Splice_Rec_385673,Human_Splice_Rec_385789,Human_Splice_Rec_385901,Human_Splice_Rec_386093,Human_Splice_Rec_386211,Human_Splice_Rec_386323,Human_Splice_Rec_386435,Human_Splice_Rec_386549,Human_Splice_Rec_386625,Human_Splice_Rec_386699,Human_Splice_Rec_386767,Human_Splice_Rec_386837 RMVar_hsa_circ_86176,RMVar_hsa_circ_97271,RMVar_hsa_circ_215503,RMVar_hsa_circ_215505,RMVar_hsa_circ_95604,RMVar_hsa_circ_215510,RMVar_hsa_circ_33939,RMVar_hsa_circ_266234,RMVar_hsa_circ_6971,RMVar_hsa_circ_309789,RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_331109,RMVar_hsa_circ_329100,RMVar_hsa_circ_118399,RMVar_hsa_circ_299518,RMVar_hsa_circ_215514,RMVar_hsa_circ_215515,RMVar_hsa_circ_65242,RMVar_hsa_circ_311933,RMVar_hsa_circ_116535,RMVar_hsa_circ_293942,RMVar_hsa_circ_342654,RMVar_hsa_circ_215519,RMVar_hsa_circ_346289,RMVar_hsa_circ_365117,RMVar_hsa_circ_365863,RMVar_hsa_circ_356709,RMVar_hsa_circ_265463,RMVar_hsa_circ_37013,RMVar_hsa_circ_2349,RMVar_hsa_circ_71586,RMVar_hsa_circ_215522,RMVar_hsa_circ_215523,RMVar_hsa_circ_215521,RMVar_hsa_circ_56169,RMVar_hsa_circ_22440,RMVar_hsa_circ_37012,RMVar_hsa_circ_215524,RMVar_hsa_circ_373151 57406 RMVar_ID_57406 Human_SNP_ID_120988817 m1A Human chr3 - 4804258 4804258 4804258 CCACCTTCTCCTCCTCCAGCTCTCAGAACTCCAATATTCTCTCTCTGTCTCCGTCCACAGGTACT CCACCTTCTCCTCCTCCAGCTCTCAGAACTCCGATATTCTCTCTCTGTCTCCGTCCACAGGTACT T C EGOT,EGOT:2 RNACentral:URS0000D5DB80,RNACentral:URS0000D59004 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:4804220..4804354 26863196 MeRIP-seq:(Medium) rs1037230897 Functional Loss SNV dbSNP153 33..33 33 - - - 57407 RMVar_ID_57407 Human_SNP_ID_121037655 m1A Human chr3 + 4979640 4979640 4979640 ACTCAGAGGAACATCTGCGGAGAGACCCCCGAAGCCCTCTCCAGGGCAGTCCTCATCCAGACGCT ACTCAGAGGAACATCTGCGGAGAGACCCCCGAGGCCCTCTCCAGGGCAGTCCTCATCCAGACGCT A G BHLHE40 Ensembl:ENSG00000134107 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:4979546..4979800 26863196 MeRIP-seq:(Medium) rs111860035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67530,Human_RBP_ID_938346,Human_RBP_ID_4756952,Human_RBP_ID_17404469,Human_RBP_ID_22455688 Human_miRNA_ID_3089880 RMVar_hsa_circ_93229,RMVar_hsa_circ_215544 57408 RMVar_ID_57408 Human_SNP_ID_121037656 m1A Human chr3 + 4979640 4979640 4979640 ACTCAGAGGAACATCTGCGGAGAGACCCCCGAAGCCCTCTCCAGGGCAGTCCTCATCCAGACGCT ACTCAGAGGAACATCTGCGGAGAGACCCCCGATGCCCTCTCCAGGGCAGTCCTCATCCAGACGCT A T BHLHE40 Ensembl:ENSG00000134107 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:4979546..4979800 26863196 MeRIP-seq:(Medium) rs111860035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67530,Human_RBP_ID_938346,Human_RBP_ID_4756952,Human_RBP_ID_17404469,Human_RBP_ID_22455688 Human_miRNA_ID_3089880 RMVar_hsa_circ_93229,RMVar_hsa_circ_215544 57409 RMVar_ID_57409 Human_SNP_ID_121037704 m1A Human chr3 + 4979742 4979742 4979742 CGCCGCGCCATGGAGCGGATCCCCAGCGCGCAACCACCCCCCGCCTGCCTGCCCAAAGCACCGGG CGCCGCGCCATGGAGCGGATCCCCAGCGCGCACCCACCCCCCGCCTGCCTGCCCAAAGCACCGGG A C BHLHE40 Ensembl:ENSG00000134107 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:4979536..4979800;chr3:4979625..4979775 26863196 MeRIP-seq:(Medium) rs776510674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783332,Human_RBP_ID_836064,Human_RBP_ID_938347,Human_RBP_ID_18471585,Human_RBP_ID_22455689,Human_RBP_ID_22533886 Human_Splice_Rec_387449,Human_Splice_Rec_387455 RMVar_hsa_circ_93229,RMVar_hsa_circ_215544 57410 RMVar_ID_57410 Human_SNP_ID_121037705 m1A Human chr3 + 4979742 4979742 4979742 CGCCGCGCCATGGAGCGGATCCCCAGCGCGCAACCACCCCCCGCCTGCCTGCCCAAAGCACCGGG CGCCGCGCCATGGAGCGGATCCCCAGCGCGCAGCCACCCCCCGCCTGCCTGCCCAAAGCACCGGG A G BHLHE40 Ensembl:ENSG00000134107 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:4979536..4979800;chr3:4979625..4979775 26863196 MeRIP-seq:(Medium) rs776510674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783332,Human_RBP_ID_836064,Human_RBP_ID_938347,Human_RBP_ID_18471585,Human_RBP_ID_22455689,Human_RBP_ID_22533886 Human_Splice_Rec_387449,Human_Splice_Rec_387455 RMVar_hsa_circ_93229,RMVar_hsa_circ_215544 57411 RMVar_ID_57411 Human_SNP_ID_121038940 m1A Human chr3 - 4983433 4983433 4983433 TGGGCAGGTAGGCAGTCGCTGAAGGTGGGATCAGGTAGAAGGGCAGGCAGAAAGGAGGCTGGTGT TGGGCAGGTAGGCAGTCGCTGAAGGTGGGATCGGGTAGAAGGGCAGGCAGAAAGGAGGCTGGTGT T C lnc-SUMF1-18 RNACentral:URS0000D5DE10 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:4983093..4983675 26863196 MeRIP-seq:(Medium) rs1360846174 Functional Loss SNV dbSNP153 33..33 33 - - - 57412 RMVar_ID_57412 Human_SNP_ID_121038949 m1A Human chr3 - 4983469 4983469 4983469 CTGGCACTGAGGTGGGATACCAGCACTTCTCCAGCATGGGCAGGTAGGCAGTCGCTGAAGGTGGG CTGGCACTGAGGTGGGATACCAGCACTTCTCCGGCATGGGCAGGTAGGCAGTCGCTGAAGGTGGG T C lnc-SUMF1-18 RNACentral:URS0000D5DE10 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:4983427..4983556 26863196 MeRIP-seq:(Medium) rs1034781310 Functional Loss SNV dbSNP153 33..33 33 - - - 57413 RMVar_ID_57413 Human_SNP_ID_121051264 m1A Human chr3 - 5026768 5026768 5026768 GAAAGAAGAACGGGTTTGGGCAAAGACACTTCAGCCCCTCCCCCCACACCCCGCGCTGGGCCTTT GAAAGAAGAACGGGTTTGGGCAAAGACACTTCCGCCCCTCCCCCCACACCCCGCGCTGGGCCTTT T G lnc-SUMF1-12,lnc-SUMF1-12:2,lnc-SUMF1-12:3,lnc-SUMF1-12:4,lnc-SUMF1-12:5,lnc-SUMF1-12:6 RNACentral:URS0000D5B0F0,RNACentral:URS00009B9C39,RNACentral:URS0000D59D83,RNACentral:URS0000D58321,RNACentral:URS0000D56E6E,RNACentral:URS0000D5E074 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:5026710..5026799 26863196 MeRIP-seq:(Medium) rs1004844802 Functional Loss SNV dbSNP153 33..33 33 - - - 57414 RMVar_ID_57414 Human_SNP_ID_121081812 m1A Human chr3 - 5122404 5122404 5122404 AGGACGGACGAGCGGCGGCGTCGACGACTTCCACACGAGCGGGCCTCCGCCCGGACCCTCCAACG AGGACGGACGAGCGGCGGCGTCGACGACTTCCTCACGAGCGGGCCTCCGCCCGGACCCTCCAACG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:5122301..5122450 26863410 MeRIP-seq:(Medium) rs558886518 Functional Loss SNV dbSNP153 33..33 33 - - - 57415 RMVar_ID_57415 Human_SNP_ID_121096364 m1A Human chr3 - 5173063 5173063 5173063 TTTCTTCCTAGCACTTAAAGCTGCATTATTCAAGTGTTTTCAGAGTATCTACCTTTCCCACTAAA TTTCTTCCTAGCACTTAAAGCTGCATTATTCAGGTGTTTTCAGAGTATCTACCTTTCCCACTAAA T C AC026202.2 Ensembl:ENSG00000233912 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:5173056..5173241 26863196 MeRIP-seq:(Medium) rs1046923636 Functional Loss SNV dbSNP153 33..33 33 - - - 57416 RMVar_ID_57416 Human_SNP_ID_121096378 m1A Human chr3 + 5173109 5173109 5173109 TTTAAGTGCTAGGAAGAAAGGTGCAAGGGGATATGAGAGTTGTAATTTAGAGGGGAGATGTGATC TTTAAGTGCTAGGAAGAAAGGTGCAAGGGGATGTGAGAGTTGTAATTTAGAGGGGAGATGTGATC A G ARL8B Ensembl:ENSG00000134108 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:5173104..5173200 26863196 MeRIP-seq:(Medium) rs574636907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24010488 RMVar_hsa_circ_59904,RMVar_hsa_circ_52082,RMVar_hsa_circ_270474,RMVar_hsa_circ_215546,RMVar_hsa_circ_91582,RMVar_hsa_circ_215551 57417 RMVar_ID_57417 Human_SNP_ID_121528695 m1A Human chr3 + 6600367 6600362 6600368 AGAAAGAAAGACGGAAAGACAGACAGACAGAAAGAGAGGGAAAAGAAAAGAAAGAGAGGAAGGAA AGAAAGAAAGACGGAAAGACAGACAGAC______AGAGGGAAAAGAAAAGAAAGAGAGGAAGGAA CAGAAAG C AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:6600333..6600459 26863196 MeRIP-seq:(Medium) rs1192642766 Functional Loss DEL dbSNP153 29..34 33 - - - 57418 RMVar_ID_57418 Human_SNP_ID_121580555 m1A Human chr3 + 6773279 6773279 6773279 GTTTAGGATTGTCTCTTCTGTCAGGAAACCTTATTAATGGAGTGTGTGGTTTGACTACCTGAACG GTTTAGGATTGTCTCTTCTGTCAGGAAACCTTGTTAATGGAGTGTGTGGTTTGACTACCTGAACG A G GRM7 Ensembl:ENSG00000196277 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:6773264..6773351 26863410 MeRIP-seq:(Medium) rs1189351174 Functional Loss SNV dbSNP153 33..33 33 - - - 57419 RMVar_ID_57419 Human_SNP_ID_122116806 m1A Human chr3 - 8751694 8751694 8751694 GAGCAGAATAAAGAGTACAGATATGAACACTTATACTTACGGTCAATTGATTTTTGACAAGGTTC GAGCAGAATAAAGAGTACAGATATGAACACTTGTACTTACGGTCAATTGATTTTTGACAAGGTTC T C OXTR Ensembl:ENSG00000180914 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:8751647..8751747 32194978 MeRIP-seq:(Medium) rs1176475954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215590 57420 RMVar_ID_57420 Human_SNP_ID_122154980 m1A Human chr3 - 8905208 8905208 8905208 TGAGTTGATTGAACGTGTACTTAGTCATGGACACTCCCACGACTAGCTGAGCCACTTAAAACTTT TGAGTTGATTGAACGTGTACTTAGTCATGGACCCTCCCACGACTAGCTGAGCCACTTAAAACTTT T G RAD18 Ensembl:ENSG00000070950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:8905193..8905345 26863196 MeRIP-seq:(Medium) rs1434521999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14957387 RMVar_hsa_circ_126710,RMVar_hsa_circ_215591,RMVar_hsa_circ_104686,RMVar_hsa_circ_84360,RMVar_hsa_circ_215596,RMVar_hsa_circ_215597,RMVar_hsa_circ_215598,RMVar_hsa_circ_215599,RMVar_hsa_circ_29354,RMVar_hsa_circ_316497,RMVar_hsa_circ_331212,RMVar_hsa_circ_347110,RMVar_hsa_circ_18857,RMVar_hsa_circ_283421,RMVar_hsa_circ_317030,RMVar_hsa_circ_51127,RMVar_hsa_circ_215601,RMVar_hsa_circ_121589 57421 RMVar_ID_57421 Human_SNP_ID_122170164 m1A Human chr3 - 8963410 8963410 8963410 GTGTTGGAGCGCCGGAGGCTAGTGGGTGGCTGACCCCCAGCATCCTCGGGAGCGACCATGGACTC GTGTTGGAGCGCCGGAGGCTAGTGGGTGGCTGGCCCCCAGCATCCTCGGGAGCGACCATGGACTC T C RAD18 Ensembl:ENSG00000070950 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:8963348..8963446 26863196 MeRIP-seq:(Medium) rs1171527499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608831,Human_RBP_ID_4757699,Human_RBP_ID_18424451,Human_RBP_ID_19011363,Human_RBP_ID_22285861,Human_RBP_ID_22457208,Human_RBP_ID_22605025 Human_Splice_Rec_388697,Human_Splice_Rec_388721,Human_Splice_Rec_388755,Human_Splice_Rec_388761,Human_Splice_Rec_388767,Human_Splice_Rec_388777,Human_Splice_Rec_388785 Human_miRNA_ID_2465792,Human_miRNA_ID_2683287 RMVar_hsa_circ_79336,RMVar_hsa_circ_215605 57422 RMVar_ID_57422 Human_SNP_ID_122170166 m1A Human chr3 + 8963412 8963412 8963412 GTCCATGGTCGCTCCCGAGGATGCTGGGGGTCAGCCACCCACTAGCCTCCGGCGCTCCAACACCA GTCCATGGTCGCTCCCGAGGATGCTGGGGGTCGGCCACCCACTAGCCTCCGGCGCTCCAACACCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:8963343..8963436 26863196 MeRIP-seq:(Medium) rs1414738293 Functional Loss SNV dbSNP153 33..33 33 - - - 57423 RMVar_ID_57423 Human_SNP_ID_122170172 m1A Human chr3 + 8963420 8963420 8963420 TCGCTCCCGAGGATGCTGGGGGTCAGCCACCCACTAGCCTCCGGCGCTCCAACACCACTCGAAAT TCGCTCCCGAGGATGCTGGGGGTCAGCCACCCCCTAGCCTCCGGCGCTCCAACACCACTCGAAAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr3:8963326..8963475;chr3:8963323..8963452 26863196 MeRIP-seq:(Medium) rs571753483 Functional Loss SNV dbSNP153 33..33 33 - - - 57424 RMVar_ID_57424 Human_SNP_ID_122269093 m1A Human chr3 - 9363119 9363119 9363119 CCGTTCCCAACCGCCGCCAGTTACCGGCCGCCAGCGAAGACCCTTTCAGCTCCCACACTCCATTG CCGTTCCCAACCGCCGCCAGTTACCGGCCGCCGGCGAAGACCCTTTCAGCTCCCACACTCCATTG T C AC026191.1,THUMPD3-AS1 Ensembl:ENSG00000254485,Ensembl:ENSG00000206573 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9363076..9363253 26863196 MeRIP-seq:(Medium) rs1559295195 Functional Loss SNV dbSNP153 33..33 33 - - - 57425 RMVar_ID_57425 Human_SNP_ID_122278839 m1A Human chr3 + 9396954 9396954 9396954 AGCCGATTTCACTGACCCTCCCCTCCCGCCGCAGGAGGCCGGCCGCGCCCGCACACCCAGCATCT AGCCGATTTCACTGACCCTCCCCTCCCGCCGCTGGAGGCCGGCCGCGCCCGCACACCCAGCATCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9396945..9397044 26863196 MeRIP-seq:(Medium) rs1168716892 Functional Loss SNV dbSNP153 33..33 33 - - - 57426 RMVar_ID_57426 Human_SNP_ID_122278861 m1A Human chr3 + 9397000 9397000 9397000 GCCCGCACACCCAGCATCTCTACACCCCACCTACCTACCCGCCCCACCCAGGGGGCAACGCGAGA GCCCGCACACCCAGCATCTCTACACCCCACCTGCCTACCCGCCCCACCCAGGGGGCAACGCGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9396963..9397060 26863196 MeRIP-seq:(Medium) rs940180570 Functional Loss SNV dbSNP153 33..33 33 - - - 57427 RMVar_ID_57427 Human_SNP_ID_122278948 m1A Human chr3 + 9397205 9397205 9397205 CTCTGCGAGAGCAATGGCTCCGTCCGGTTTCGAGCATTTTCCGCTCCCTTCTCCCTCCCCCTCCG CTCTGCGAGAGCAATGGCTCCGTCCGGTTTCGCGCATTTTCCGCTCCCTTCTCCCTCCCCCTCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9397198..9397458 26863196 MeRIP-seq:(Medium) rs181526446 Functional Loss SNV dbSNP153 33..33 33 - - - 57428 RMVar_ID_57428 Human_SNP_ID_122278949 m1A Human chr3 + 9397205 9397205 9397205 CTCTGCGAGAGCAATGGCTCCGTCCGGTTTCGAGCATTTTCCGCTCCCTTCTCCCTCCCCCTCCG CTCTGCGAGAGCAATGGCTCCGTCCGGTTTCGTGCATTTTCCGCTCCCTTCTCCCTCCCCCTCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9397198..9397458 26863196 MeRIP-seq:(Medium) rs181526446 Functional Loss SNV dbSNP153 33..33 33 - - - 57429 RMVar_ID_57429 Human_SNP_ID_122278963 m1A Human chr3 - 9397240 9397240 9397240 GATGCAGGCGGGAGGGAGGCCCGCCCTGCGGCAACCGGAGGGGGAGGGAGAAGGGAGCGGAAAAT GATGCAGGCGGGAGGGAGGCCCGCCCTGCGGCCACCGGAGGGGGAGGGAGAAGGGAGCGGAAAAT T G THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9397196..9397382 26863196 MeRIP-seq:(Medium) rs1385398379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266384,Human_RBP_ID_785388,Human_RBP_ID_835087,Human_RBP_ID_3720690,Human_RBP_ID_5089658,Human_RBP_ID_5120899,Human_RBP_ID_5149868,Human_RBP_ID_5241470,Human_RBP_ID_5389830,Human_RBP_ID_5654816,Human_RBP_ID_8124501,Human_RBP_ID_8209125,Human_RBP_ID_8235785,Human_RBP_ID_8943538,Human_RBP_ID_9434517,Human_RBP_ID_17195047,Human_RBP_ID_17208803,Human_RBP_ID_17660779,Human_RBP_ID_18464326,Human_RBP_ID_18499538,Human_RBP_ID_18953293,Human_RBP_ID_19119277,Human_RBP_ID_21986785,Human_RBP_ID_22701623,Human_RBP_ID_22725566,Human_RBP_ID_23288101,Human_RBP_ID_24553925,Human_RBP_ID_25759845,Human_RBP_ID_26771176,Human_RBP_ID_26790082 57430 RMVar_ID_57430 Human_SNP_ID_122279265 m1A Human chr3 + 9397696 9397696 9397696 GCCGCCGCCGCCGCCGCCGCCGCTGCCGGGGGAGGGGCGGCCGCCGCCCGCCTGCGCTCAGAGAC GCCGCCGCCGCCGCCGCCGCCGCTGCCGGGGGGGGGGCGGCCGCCGCCCGCCTGCGCTCAGAGAC A G SETD5 Ensembl:ENSG00000168137 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:9397649..9397784 26863196 MeRIP-seq:(Medium) rs1038814401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756961,Human_RBP_ID_5325428,Human_RBP_ID_9333592,Human_RBP_ID_17404483,Human_RBP_ID_18423922,Human_RBP_ID_18499540,Human_RBP_ID_22533887 57431 RMVar_ID_57431 Human_SNP_ID_122292342 m1A Human chr3 + 9445195 9445195 9445195 ATTGGAGCAGAGACTAGACGTAGAAAAGCACGACGGAAAGAGCTAGAGATGGAGCAGCAGAATGA ATTGGAGCAGAGACTAGACGTAGAAAAGCACGGCGGAAAGAGCTAGAGATGGAGCAGCAGAATGA A G SETD5 Ensembl:ENSG00000168137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9445145..9445247 26863196 MeRIP-seq:(Medium) rs1267570577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835599,Human_RBP_ID_5602853,Human_RBP_ID_14963324,Human_RBP_ID_22825052,Human_RBP_ID_25760603 Human_miRNA_ID_1968205 RMVar_hsa_circ_301307,RMVar_hsa_circ_329981,RMVar_hsa_circ_342583,RMVar_hsa_circ_44841,RMVar_hsa_circ_67104,RMVar_hsa_circ_315370,RMVar_hsa_circ_13045,RMVar_hsa_circ_342894,RMVar_hsa_circ_353608,RMVar_hsa_circ_62908,RMVar_hsa_circ_334353,RMVar_hsa_circ_55533,RMVar_hsa_circ_104460,RMVar_hsa_circ_337,RMVar_hsa_circ_85055,RMVar_hsa_circ_353233,RMVar_hsa_circ_215646,RMVar_hsa_circ_374649,RMVar_hsa_circ_121045,RMVar_hsa_circ_215654,RMVar_hsa_circ_215656,RMVar_hsa_circ_215655,RMVar_hsa_circ_63101,RMVar_hsa_circ_267667,RMVar_hsa_circ_332102,RMVar_hsa_circ_72505,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_43807,RMVar_hsa_circ_346618,RMVar_hsa_circ_280813,RMVar_hsa_circ_215663,RMVar_hsa_circ_302892,RMVar_hsa_circ_215661,RMVar_hsa_circ_359261,RMVar_hsa_circ_271779,RMVar_hsa_circ_215662 57432 RMVar_ID_57432 Human_SNP_ID_122298936 m1A Human chr3 + 9467317 9467317 9467317 AATGGTGAGAAGTCTTAAGTGCTAAGGGGAAGAAGGTAAGAAGATAAACAGTGGAAGAGAACAAG AATGGTGAGAAGTCTTAAGTGCTAAGGGGAAGGAGGTAAGAAGATAAACAGTGGAAGAGAACAAG A G SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:9467273..9467398 26863196 MeRIP-seq:(Medium) rs1004112608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7233991,Human_RBP_ID_14963989,Human_RBP_ID_18815674,Human_RBP_ID_23026043,Human_RBP_ID_23288066,Human_RBP_ID_24547370 RMVar_hsa_circ_329981,RMVar_hsa_circ_315370,RMVar_hsa_circ_353608,RMVar_hsa_circ_62908,RMVar_hsa_circ_85055,RMVar_hsa_circ_353233,RMVar_hsa_circ_121045,RMVar_hsa_circ_215656,RMVar_hsa_circ_215655,RMVar_hsa_circ_62211,RMVar_hsa_circ_43807,RMVar_hsa_circ_60549,RMVar_hsa_circ_74772,RMVar_hsa_circ_118676,RMVar_hsa_circ_114369,RMVar_hsa_circ_215664,RMVar_hsa_circ_215665,RMVar_hsa_circ_366958 57433 RMVar_ID_57433 Human_SNP_ID_122299275 m1A Human chr3 - 9468669 9468669 9468669 GAGTGGCCGCCCTCCAGCCCATCACCCCACTGACTCAGATCCCCAGCCCTCCCCACACACTCAGG GAGTGGCCGCCCTCCAGCCCATCACCCCACTGTCTCAGATCCCCAGCCCTCCCCACACACTCAGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9468619..9468916 26863196 MeRIP-seq:(Medium) rs1327602399 Functional Loss SNV dbSNP153 33..33 33 - - - 57434 RMVar_ID_57434 Human_SNP_ID_122301269 m1A Human chr3 + 9475609 9475609 9475609 ACAGTTATCGAACTACTGCACTGAGACCTGGAAACCCCCCCTCTCACGGTTCTTCAGAATCATCC ACAGTTATCGAACTACTGCACTGAGACCTGGAGACCCCCCCTCTCACGGTTCTTCAGAATCATCC A G SETD5 Ensembl:ENSG00000168137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9475558..9475712 26863196 MeRIP-seq:(Medium) rs1297918468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609057,Human_RBP_ID_7234081,Human_RBP_ID_8874620,Human_RBP_ID_14964224,Human_RBP_ID_17291089,Human_RBP_ID_17404395,Human_RBP_ID_17521182,Human_RBP_ID_18815709,Human_RBP_ID_18954112,Human_RBP_ID_27504868 RMVar_hsa_circ_112912,RMVar_hsa_circ_215670 57435 RMVar_ID_57435 Human_SNP_ID_122301959 m1A Human chr3 + 9477896 9477896 9477896 TGCATTCTCCCCTTGGCTATTTAACCAAGGGGAGAGGCCAGCGGGCAGGCGGCCCTCACCCTGCC TGCATTCTCCCCTTGGCTATTTAACCAAGGGGCGAGGCCAGCGGGCAGGCGGCCCTCACCCTGCC A C SETD5 Ensembl:ENSG00000168137 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9477846..9477940 26863196 MeRIP-seq:(Medium) rs1361902985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247728,Human_RBP_ID_5120181,Human_RBP_ID_7234173,Human_RBP_ID_18012153,Human_RBP_ID_18341706,Human_RBP_ID_21897349,Human_RBP_ID_22825098 RMVar_hsa_circ_112912,RMVar_hsa_circ_215670 57436 RMVar_ID_57436 Human_SNP_ID_122350280 m1A Human chr3 - 9649527 9649527 9649527 GTGCCTCAAGCGGGCCCATGGCACCTGCCTGCACCCAACTCCGACACTAGAACCTCCGGAACCGC GTGCCTCAAGCGGGCCCATGGCACCTGCCTGCCCCCAACTCCGACACTAGAACCTCCGGAACCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9649476..9649791 26863196 MeRIP-seq:(Medium) rs1366534660 Functional Loss SNV dbSNP153 33..33 33 - - - 57437 RMVar_ID_57437 Human_SNP_ID_122350288 m1A Human chr3 - 9649537 9649537 9649537 TCCCCTCAGTGTGCCTCAAGCGGGCCCATGGCACCTGCCTGCACCCAACTCCGACACTAGAACCT TCCCCTCAGTGTGCCTCAAGCGGGCCCATGGCGCCTGCCTGCACCCAACTCCGACACTAGAACCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:9649489..9649658;chr3:9649491..9649672 26863196 MeRIP-seq:(Medium) rs1342041667 Functional Loss SNV dbSNP153 33..33 33 - - - 57438 RMVar_ID_57438 Human_SNP_ID_122364900 m1A Human chr3 + 9702125 9702125 9702125 CATCATGAACATGGCAGCCCCAAAGCTGAGCAAGGCCAAAGACAGGGTTTTCCAACCCCCAGCCT CATCATGAACATGGCAGCCCCAAAGCTGAGCACGGCCAAAGACAGGGTTTTCCAACCCCCAGCCT A C MTMR14 Ensembl:ENSG00000163719 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9702076..9702343 32194978 MeRIP-seq:(Medium) rs1221083967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5120900 RMVar_hsa_circ_115827,RMVar_hsa_circ_215673 57439 RMVar_ID_57439 Human_SNP_ID_122373474 m1A Human chr3 + 9731796 9731796 9731796 CTGCCGCCGCCGCTGCCACAGCCTTTGCCGCCACGGTCTCCGCCGCCGCTGTCCTCGCGCTGCCT CTGCCGCCGCCGCTGCCACAGCCTTTGCCGCCGCGGTCTCCGCCGCCGCTGTCCTCGCGCTGCCT A G BRPF1 Ensembl:ENSG00000156983 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:9731747..9731894 26863196 MeRIP-seq:(Medium) rs1355623928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4755289,Human_RBP_ID_5392473,Human_RBP_ID_5447970,Human_RBP_ID_9334054,Human_RBP_ID_18815892,Human_RBP_ID_22286245,Human_RBP_ID_27504980 57440 RMVar_ID_57440 Human_SNP_ID_122373544 m1A Human chr3 + 9731981 9731980 9731981 AGGGGTCAGCTCAGGAATCCCGGGGAGCCGGGACCAAAGCGTGGGGCGGCAGGGGGCCGGGGTGG AGGGGTCAGCTCAGGAATCCCGGGGAGCCGGG_CCAAAGCGTGGGGCGGCAGGGGGCCGGGGTGG GA G BRPF1 Ensembl:ENSG00000156983 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9731755..9732050 26863196 MeRIP-seq:(Medium) rs1407640560 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22455312 57441 RMVar_ID_57441 Human_SNP_ID_122375695 m1A Human chr3 + 9739850 9739850 9739850 TGAGGGTAAGGGCTGGAGCTCAGAGAAAGTCAAGAAGGCCAAGGCCAAGTCCCGGATCAAAATGA TGAGGGTAAGGGCTGGAGCTCAGAGAAAGTCAGGAAGGCCAAGGCCAAGTCCCGGATCAAAATGA A G BRPF1 Ensembl:ENSG00000156983 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9739801..9739904 26863196 MeRIP-seq:(Medium) rs139007155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26346441 RMVar_hsa_circ_70033,RMVar_hsa_circ_39143 57442 RMVar_ID_57442 Human_SNP_ID_122377057 m1A Human chr3 - 9744387 9744387 9744387 GAACTCATGATGGGGAGCTGGGGGGGCCCCACAGGACTGCCTCCGTGGCTGGGGGTCATCTGGCT GAACTCATGATGGGGAGCTGGGGGGGCCCCACGGGACTGCCTCCGTGGCTGGGGGTCATCTGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9744342..9744447 26863196 MeRIP-seq:(Medium) rs1358447010 Functional Loss SNV dbSNP153 33..33 33 - - - 57443 RMVar_ID_57443 Human_SNP_ID_122377072 m1A Human chr3 + 9744401 9744400 9744402 CAGCCACGGAGGCAGTCCTGTGGGGCCCCCCCAGCTCCCCATCATGAGTTCCCTGCGTCAGCGCA CAGCCACGGAGGCAGTCCTGTGGGGCCCCCCC__CTCCCCATCATGAGTTCCCTGCGTCAGCGCA CAG C BRPF1 Ensembl:ENSG00000156983 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:9744350..9744500 26863196 MeRIP-seq:(Medium) rs1245919644 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4755348 Human_miRNA_ID_2366151,Human_miRNA_ID_2616987,Human_miRNA_ID_2683292,Human_miRNA_ID_3013960 RMVar_hsa_circ_36037,RMVar_hsa_circ_49656,RMVar_hsa_circ_215686,RMVar_hsa_circ_372988,RMVar_hsa_circ_38386,RMVar_hsa_circ_344417 57444 RMVar_ID_57444 Human_SNP_ID_122377073 m1A Human chr3 + 9744401 9744401 9744401 CAGCCACGGAGGCAGTCCTGTGGGGCCCCCCCAGCTCCCCATCATGAGTTCCCTGCGTCAGCGCA CAGCCACGGAGGCAGTCCTGTGGGGCCCCCCCGGCTCCCCATCATGAGTTCCCTGCGTCAGCGCA A G BRPF1 Ensembl:ENSG00000156983 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:9744350..9744500 26863196 MeRIP-seq:(Medium) rs372788717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4755348 Human_miRNA_ID_2366151,Human_miRNA_ID_2616987,Human_miRNA_ID_2683292,Human_miRNA_ID_3013960 RMVar_hsa_circ_36037,RMVar_hsa_circ_49656,RMVar_hsa_circ_215686,RMVar_hsa_circ_372988,RMVar_hsa_circ_38386,RMVar_hsa_circ_344417 57445 RMVar_ID_57445 Human_SNP_ID_122380779 m1A Human chr3 + 9756551 9756551 9756551 CCCGTGGATGTCCATATGTGGCACATTGCCCAACGTGACTACAGCTGGCACCCTACCACGTCCCA CCCGTGGATGTCCATATGTGGCACATTGCCCAGCGTGACTACAGCTGGCACCCTACCACGTCCCA A G OGG1 Ensembl:ENSG00000114026 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9754717..9756553 32194978 MeRIP-seq:(Medium) rs138147246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14968319,Human_RBP_ID_18815921 Human_Splice_Rec_390460,Human_Splice_Rec_390461,Human_Splice_Rec_390472,Human_Splice_Rec_390473,Human_Splice_Rec_390492,Human_Splice_Rec_390493,Human_Splice_Rec_390504,Human_Splice_Rec_390505,Human_Splice_Rec_390516,Human_Splice_Rec_390517,Human_Splice_Rec_390530,Human_Splice_Rec_390531,Human_Splice_Rec_390538,Human_Splice_Rec_390539,Human_Splice_Rec_390552,Human_Splice_Rec_390553,Human_Splice_Rec_390560,Human_Splice_Rec_390561,Human_Splice_Rec_390580,Human_Splice_Rec_390581 GWAS_ID_6721,GWAS_ID_6722 RMVar_hsa_circ_84285,RMVar_hsa_circ_292327,RMVar_hsa_circ_215688,RMVar_hsa_circ_215689,RMVar_hsa_circ_363095,RMVar_hsa_circ_379004 57446 RMVar_ID_57446 Human_SNP_ID_122380915 m1A Human chr3 + 9756989 9756989 9756989 GCCCTGTTCCCCAAGGACTCTTCCACCTCCCAACACTGTCACTAGTCTCACCAGCCCTGACCCCA GCCCTGTTCCCCAAGGACTCTTCCACCTCCCAGCACTGTCACTAGTCTCACCAGCCCTGACCCCA A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9756943..9757030 26863196 MeRIP-seq:(Medium) rs373863564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5133170,Human_RBP_ID_17088494,Human_RBP_ID_17404858,Human_RBP_ID_18954117,Human_RBP_ID_27505013 RMVar_hsa_circ_292327,RMVar_hsa_circ_215688 57447 RMVar_ID_57447 Human_SNP_ID_122381417 m1A Human chr3 + 9758391 9758391 9758391 TAACCATCTCAGTCATGGTACCACCACCATCCATTCTGTTCCCAGCCACAGTCTTGGGCCAGCCC TAACCATCTCAGTCATGGTACCACCACCATCCGTTCTGTTCCCAGCCACAGTCTTGGGCCAGCCC A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9758388..9758590 26863196 MeRIP-seq:(Medium) rs1486419521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292327,RMVar_hsa_circ_215688 57448 RMVar_ID_57448 Human_SNP_ID_122381442 m1A Human chr3 + 9758470 9758470 9758470 CCCCAACATCCATTGCATCGTCATGTCTTGTCAGTTTCACCTCCTAAATGACTCCTGGATCAACC CCCCAACATCCATTGCATCGTCATGTCTTGTCCGTTTCACCTCCTAAATGACTCCTGGATCAACC A C OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9758466..9758560 26863196 MeRIP-seq:(Medium) rs1260388466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580638 RMVar_hsa_circ_292327,RMVar_hsa_circ_215688 57449 RMVar_ID_57449 Human_SNP_ID_122382142 m1A Human chr3 - 9760791 9760791 9760791 CCCGGAGCCAACGGCACCCGAAAGTGGAAATGAGGATGAGTTTCTCCCTGCCCAGGCTCTGCGGT CCCGGAGCCAACGGCACCCGAAAGTGGAAATGCGGATGAGTTTCTCCCTGCCCAGGCTCTGCGGT T G CAMK1 Ensembl:ENSG00000134072 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9760788..9760889 32194978 MeRIP-seq:(Medium) rs376144816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18815930 RMVar_hsa_circ_101448,RMVar_hsa_circ_125240,RMVar_hsa_circ_72000,RMVar_hsa_circ_215694,RMVar_hsa_circ_91953,RMVar_hsa_circ_215695,RMVar_hsa_circ_215696,RMVar_hsa_circ_305707,RMVar_hsa_circ_34368 57450 RMVar_ID_57450 Human_SNP_ID_122382339 m1A Human chr3 + 9761462 9761462 9761462 CCACAGCCTACCATGGCCAAGCCCCACTTACAAGATGTAGGCGATGACACCTATGGACCAGCAAT CCACAGCCTACCATGGCCAAGCCCCACTTACAGGATGTAGGCGATGACACCTATGGACCAGCAAT A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9761451..9761475 32194978 MeRIP-seq:(Medium) rs1327064915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14968350 57451 RMVar_ID_57451 Human_SNP_ID_122382883 m1A Human chr3 - 9763170 9763168 9763170 CCAACATTGTAGCCCTGGATGACATCTATGAGAGTGGGGGCCACCTCTACCTCATCATGCAGCTG CCAACATTGTAGCCCTGGATGACATCTATGAG__TGGGGGCCACCTCTACCTCATCATGCAGCTG ACT A CAMK1 Ensembl:ENSG00000134072 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9763165..9765860 32194978 MeRIP-seq:(Medium) rs1446869253 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_933559 Human_Splice_Rec_390594,Human_Splice_Rec_390595,Human_Splice_Rec_390630,Human_Splice_Rec_390631,Human_Splice_Rec_390648,Human_Splice_Rec_390649 Human_miRNA_ID_2375,Human_miRNA_ID_6050,Human_miRNA_ID_9657,Human_miRNA_ID_13193,Human_miRNA_ID_16795,Human_miRNA_ID_20443,Human_miRNA_ID_24081,Human_miRNA_ID_27750,Human_miRNA_ID_1306755 RMVar_hsa_circ_101448,RMVar_hsa_circ_125240,RMVar_hsa_circ_215695,RMVar_hsa_circ_215696,RMVar_hsa_circ_305707,RMVar_hsa_circ_215700,RMVar_hsa_circ_215698,RMVar_hsa_circ_107796,RMVar_hsa_circ_291469,RMVar_hsa_circ_113646,RMVar_hsa_circ_215699 57452 RMVar_ID_57452 Human_SNP_ID_122383664 m1A Human chr3 - 9765858 9765858 9765858 GGGGGCCTTCTCGGAGGTGATCCTGGCAGAAGATAAGAGGACGCAGAAGCTGGTGGCCATCAAAT GGGGGCCTTCTCGGAGGTGATCCTGGCAGAAGGTAAGAGGACGCAGAAGCTGGTGGCCATCAAAT T C CAMK1 Ensembl:ENSG00000134072 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9765808..9765935 26863196 MeRIP-seq:(Medium) rs775439790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393275 Human_Splice_Rec_390592,Human_Splice_Rec_390593,Human_Splice_Rec_390628,Human_Splice_Rec_390629 Human_miRNA_ID_1348314 GWAS_ID_6723,GWAS_ID_6724,GWAS_ID_6725,GWAS_ID_6726 RMVar_hsa_circ_101448,RMVar_hsa_circ_125240,RMVar_hsa_circ_215695,RMVar_hsa_circ_215696,RMVar_hsa_circ_215698,RMVar_hsa_circ_107796,RMVar_hsa_circ_113646,RMVar_hsa_circ_215699,RMVar_hsa_circ_215702 57453 RMVar_ID_57453 Human_SNP_ID_122387527 m1A Human chr3 - 9780535 9780532 9780535 GCTGGCTGGTCCCCACAGGCTGGCAAAGGAGGAGGTGAGCCGGCAGGAGCTGAGGCAGCGGGTGC GCTGGCTGGTCCCCACAGGCTGGCAAAGGAGG___TGAGCCGGCAGGAGCTGAGGCAGCGGGTGC ACCT A TADA3 Ensembl:ENSG00000171148 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9780376..9780592 26863196 MeRIP-seq:(Medium) rs764925976 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_938875 Human_Splice_Rec_390668,Human_Splice_Rec_390676,Human_Splice_Rec_390692 RMVar_hsa_circ_90942,RMVar_hsa_circ_215703 57454 RMVar_ID_57454 Human_SNP_ID_122389479 m1A Human chr3 + 9787112 9787112 9787112 CCTCAGACTTCTTCAGCAGGGCATCCACATCTAAGCGGGCACAGGAAAGGAGGGGAGGTGGGCTG CCTCAGACTTCTTCAGCAGGGCATCCACATCTGAGCGGGCACAGGAAAGGAGGGGAGGTGGGCTG A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9787110..9787190 26863196 MeRIP-seq:(Medium) rs1464483853 Functional Loss SNV dbSNP153 33..33 33 - - - 57455 RMVar_ID_57455 Human_SNP_ID_122389546 m1A Human chr3 + 9787254 9787254 9787254 GGCCCCATGAGGCCTTTCTTCTTGTCAGCCACAGCCGCTGCCCGGGCCCCATCCTTCTGCTCCTC GGCCCCATGAGGCCTTTCTTCTTGTCAGCCACGGCCGCTGCCCGGGCCCCATCCTTCTGCTCCTC A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9787206..9787293 26863196 MeRIP-seq:(Medium) rs777162351 Functional Loss SNV dbSNP153 33..33 33 - - - 57456 RMVar_ID_57456 Human_SNP_ID_122390381 m1A Human chr3 - 9789856 9789856 9789856 CCCCCCAAACATGGGAAGCCCAAGAAGCAGAAACTGGAAGGGAAGGCAGGACATGGGCCGGGCCC CCCCCCAAACATGGGAAGCCCAAGAAGCAGAACCTGGAAGGGAAGGCAGGACATGGGCCGGGCCC T G TADA3 Ensembl:ENSG00000171148 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9789720..9789899 26863196 MeRIP-seq:(Medium) rs1409232331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580680,Human_RBP_ID_18815965,Human_RBP_ID_27322885 RMVar_hsa_circ_4211,RMVar_hsa_circ_109034,RMVar_hsa_circ_215704 57457 RMVar_ID_57457 Human_SNP_ID_122393043 m1A Human chr3 + 9797678 9797678 9797678 TTATTTCCTATAGACTGCCACTCTCCGCCCCTACCTGAGTGCCGTGCGGGCCACATTGCAGGCTG TTATTTCCTATAGACTGCCACTCTCCGCCCCTGCCTGAGTGCCGTGCGGGCCACATTGCAGGCTG A G ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:9793081..9797833 26863196 MeRIP-seq:(Medium) rs755000138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784094,Human_RBP_ID_835810,Human_RBP_ID_934726,Human_RBP_ID_4756971,Human_RBP_ID_9333595,Human_RBP_ID_26346446 Human_Splice_Rec_390716,Human_Splice_Rec_390717,Human_Splice_Rec_390726,Human_Splice_Rec_390727,Human_Splice_Rec_390736,Human_Splice_Rec_390738,Human_Splice_Rec_390739,Human_Splice_Rec_390750,Human_Splice_Rec_390751,Human_Splice_Rec_390762,Human_Splice_Rec_390763,Human_Splice_Rec_390769,Human_Splice_Rec_390776,Human_Splice_Rec_390777,Human_Splice_Rec_390786,Human_Splice_Rec_390787,Human_Splice_Rec_390794,Human_Splice_Rec_390795,Human_Splice_Rec_390808,Human_Splice_Rec_390809,Human_Splice_Rec_390829 Human_miRNA_ID_2769871,Human_miRNA_ID_2769872,Human_miRNA_ID_2769873 RMVar_hsa_circ_6194,RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_274210,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708,RMVar_hsa_circ_299260,RMVar_hsa_circ_366727,RMVar_hsa_circ_287945,RMVar_hsa_circ_48815,RMVar_hsa_circ_83967,RMVar_hsa_circ_10453,RMVar_hsa_circ_215710,RMVar_hsa_circ_215711,RMVar_hsa_circ_215709 57458 RMVar_ID_57458 Human_SNP_ID_122395563 m1A Human chr3 - 9806327 9806327 9806327 AGCACACCACCCACCTCCCGCATCAAATGCCCACCCCAACCCAACTCCCTGCCGCCGCCGCGCTG AGCACACCACCCACCTCCCGCATCAAATGCCCTCCCCAACCCAACTCCCTGCCGCCGCCGCGCTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9806276..9806442 26863196 MeRIP-seq:(Medium) rs1159573984 Functional Loss SNV dbSNP153 33..33 33 - - - 57459 RMVar_ID_57459 Human_SNP_ID_122395567 m1A Human chr3 - 9806356 9806356 9806356 TCCACTGCTGCTTTCTTGCCCAGCTAGCAAGCACACCACCCACCTCCCGCATCAAATGCCCACCC TCCACTGCTGCTTTCTTGCCCAGCTAGCAAGCTCACCACCCACCTCCCGCATCAAATGCCCACCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9806201..9806444 26863196 MeRIP-seq:(Medium) rs958709787 Functional Loss SNV dbSNP153 33..33 33 - - - 57460 RMVar_ID_57460 Human_SNP_ID_122396899 m1A Human chr3 - 9810382 9810380 9810382 GCGGGCCGCACGGGCCTCACCATCCTGCGGAGAGGGGTCGAGGACCGGGGTGTGCGGGGGGCCGA GCGGGCCGCACGGGCCTCACCATCCTGCGGAG__GGGTCGAGGACCGGGGTGTGCGGGGGGCCGA CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9809912..9810648 26863196 MeRIP-seq:(Medium) rs1265853670 Functional Loss DEL dbSNP153 33..34 33 - - - 57461 RMVar_ID_57461 Human_SNP_ID_122399682 m1A Human chr3 - 9820533 9820533 9820533 TTTCTTGGGCTGCTTGTCTCCTGCACATAGGGAGGGGCCTGTCACGATCCCATATCAAGGCAGGT TTTCTTGGGCTGCTTGTCTCCTGCACATAGGGCGGGGCCTGTCACGATCCCATATCAAGGCAGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9820289..9820539 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 57462 RMVar_ID_57462 Human_SNP_ID_122399773 m1A Human chr3 + 9820741 9820741 9820741 CCTCTTCCTCCAGCGCTACTACCAAGTGGTCCAGTGAGTCCCCTGCAGCTGGGACTTTGGGCTGT CCTCTTCCTCCAGCGCTACTACCAAGTGGTCCCGTGAGTCCCCTGCAGCTGGGACTTTGGGCTGT A C ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9820738..9820838 32194978 MeRIP-seq:(Medium) rs376121879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580768,Human_RBP_ID_9394600,Human_RBP_ID_18816093,Human_RBP_ID_19011414 Human_Splice_Rec_390821,Human_Splice_Rec_390919,Human_Splice_Rec_390939,Human_Splice_Rec_390995,Human_Splice_Rec_391011,Human_Splice_Rec_391023,Human_Splice_Rec_391053,Human_Splice_Rec_391061,Human_Splice_Rec_391073,Human_Splice_Rec_391081,Human_Splice_Rec_391093,Human_Splice_Rec_391101,Human_Splice_Rec_391111 RMVar_hsa_circ_344559,RMVar_hsa_circ_346108 57463 RMVar_ID_57463 Human_SNP_ID_122399774 m1A Human chr3 + 9820741 9820741 9820741 CCTCTTCCTCCAGCGCTACTACCAAGTGGTCCAGTGAGTCCCCTGCAGCTGGGACTTTGGGCTGT CCTCTTCCTCCAGCGCTACTACCAAGTGGTCCGGTGAGTCCCCTGCAGCTGGGACTTTGGGCTGT A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9820738..9820838 32194978 MeRIP-seq:(Medium) rs376121879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580768,Human_RBP_ID_9394600,Human_RBP_ID_18816093,Human_RBP_ID_19011414 Human_Splice_Rec_390821,Human_Splice_Rec_390919,Human_Splice_Rec_390939,Human_Splice_Rec_390995,Human_Splice_Rec_391011,Human_Splice_Rec_391023,Human_Splice_Rec_391053,Human_Splice_Rec_391061,Human_Splice_Rec_391073,Human_Splice_Rec_391081,Human_Splice_Rec_391093,Human_Splice_Rec_391101,Human_Splice_Rec_391111 RMVar_hsa_circ_344559,RMVar_hsa_circ_346108 57464 RMVar_ID_57464 Human_SNP_ID_122402294 m1A Human chr3 - 9829360 9829360 9829360 CTTATAGATGAGCTCAAAGGCTCCTGTGTCACAGTTGCGGTCCAGCATCCGGTCAATGACCACGC CTTATAGATGAGCTCAAAGGCTCCTGTGTCACTGTTGCGGTCCAGCATCCGGTCAATGACCACGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9829309..9833118 32194978 MeRIP-seq:(Medium) rs1487916947 Functional Loss SNV dbSNP153 33..33 33 - - - 57465 RMVar_ID_57465 Human_SNP_ID_122405007 m1A Human chr3 + 9838206 9838206 9838206 GGTGGAGGCGTCTGAGGAGGGCTTCATCCAGGACCTGGAGCGGGAGAGGTACGTTGTGTTCAGCC GGTGGAGGCGTCTGAGGAGGGCTTCATCCAGGGCCTGGAGCGGGAGAGGTACGTTGTGTTCAGCC A G TTLL3 Ensembl:ENSG00000214021 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9837898..9839026 32194978 MeRIP-seq:(Medium) rs369448971 Functional Loss SNV dbSNP153 33..33 33 - - - 57466 RMVar_ID_57466 Human_SNP_ID_122405008 m1A Human chr3 + 9838206 9838206 9838206 GGTGGAGGCGTCTGAGGAGGGCTTCATCCAGGACCTGGAGCGGGAGAGGTACGTTGTGTTCAGCC GGTGGAGGCGTCTGAGGAGGGCTTCATCCAGGTCCTGGAGCGGGAGAGGTACGTTGTGTTCAGCC A T TTLL3 Ensembl:ENSG00000214021 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9837898..9839026 32194978 MeRIP-seq:(Medium) rs369448971 Functional Loss SNV dbSNP153 33..33 33 - - - 57467 RMVar_ID_57467 Human_SNP_ID_122406643 m1A Human chr3 - 9843599 9843599 9843599 GACTCCCATTGCTTCTCCCTCCTTGTCCAGGCATCAGAGGCAACCCCGCGGCTCCTGCCAACGGT GACTCCCATTGCTTCTCCCTCCTTGTCCAGGCTTCAGAGGCAACCCCGCGGCTCCTGCCAACGGT T A RPUSD3 Ensembl:ENSG00000156990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9843520..9843653 26863196 MeRIP-seq:(Medium) rs760554242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756973,Human_RBP_ID_5325118 Human_Splice_Rec_391142,Human_Splice_Rec_391156,Human_Splice_Rec_391178,Human_Splice_Rec_391192,Human_Splice_Rec_391212,Human_Splice_Rec_391218,Human_Splice_Rec_391236,Human_Splice_Rec_391248,Human_Splice_Rec_391258 57468 RMVar_ID_57468 Human_SNP_ID_122406644 m1A Human chr3 - 9843599 9843599 9843599 GACTCCCATTGCTTCTCCCTCCTTGTCCAGGCATCAGAGGCAACCCCGCGGCTCCTGCCAACGGT GACTCCCATTGCTTCTCCCTCCTTGTCCAGGCGTCAGAGGCAACCCCGCGGCTCCTGCCAACGGT T C RPUSD3 Ensembl:ENSG00000156990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9843520..9843653 26863196 MeRIP-seq:(Medium) rs760554242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756973,Human_RBP_ID_5325118 Human_Splice_Rec_391142,Human_Splice_Rec_391156,Human_Splice_Rec_391178,Human_Splice_Rec_391192,Human_Splice_Rec_391212,Human_Splice_Rec_391218,Human_Splice_Rec_391236,Human_Splice_Rec_391248,Human_Splice_Rec_391258 57469 RMVar_ID_57469 Human_SNP_ID_122406826 m1A Human chr3 + 9843951 9843951 9843951 GGGCACTGGGCGGACACCCAGGCCCCGCCGCCAGCCACTCCAGAACCGGCCCAAAACACGGCGGC GGGCACTGGGCGGACACCCAGGCCCCGCCGCCGGCCACTCCAGAACCGGCCCAAAACACGGCGGC A G TTLL3 Ensembl:ENSG00000214021 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9843834..9843958 26863196 MeRIP-seq:(Medium) rs777725369 Functional Loss SNV dbSNP153 33..33 33 - - - 57470 RMVar_ID_57470 Human_SNP_ID_122406837 m1A Human chr3 + 9843962 9843962 9843962 GGACACCCAGGCCCCGCCGCCAGCCACTCCAGAACCGGCCCAAAACACGGCGGCCGTCCATCTCC GGACACCCAGGCCCCGCCGCCAGCCACTCCAGCACCGGCCCAAAACACGGCGGCCGTCCATCTCC A C TTLL3 Ensembl:ENSG00000214021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9843707..9844000 26863196 MeRIP-seq:(Medium) rs369545840 Functional Loss SNV dbSNP153 33..33 33 - - - 57471 RMVar_ID_57471 Human_SNP_ID_122406838 m1A Human chr3 + 9843962 9843962 9843962 GGACACCCAGGCCCCGCCGCCAGCCACTCCAGAACCGGCCCAAAACACGGCGGCCGTCCATCTCC GGACACCCAGGCCCCGCCGCCAGCCACTCCAGTACCGGCCCAAAACACGGCGGCCGTCCATCTCC A T TTLL3 Ensembl:ENSG00000214021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9843707..9844000 26863196 MeRIP-seq:(Medium) rs369545840 Functional Loss SNV dbSNP153 33..33 33 - - - 57472 RMVar_ID_57472 Human_SNP_ID_122420437 m1A Human chr3 + 9890830 9890830 9890830 CACTACCAGATGAGGTATGAAGTGAGGCGAGGAGCACGGAGGCTTTCTCCCCCGCTGGAGCCTGC CACTACCAGATGAGGTATGAAGTGAGGCGAGGGGCACGGAGGCTTTCTCCCCCGCTGGAGCCTGC A G JAGN1 Ensembl:ENSG00000171135 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9890827..9891002 26863196 MeRIP-seq:(Medium) rs1467017763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115011,Human_RBP_ID_22092179 57473 RMVar_ID_57473 Human_SNP_ID_122420486 m1A Human chr3 - 9890939 9890936 9890939 ATGGGGGACAGGCCCGAAGCCGTCACGGGAGGAGGGGACTTGGCAGGTGAGCGGGGGCTGGCTGG ATGGGGGACAGGCCCGAAGCCGTCACGGGAGG___GGACTTGGCAGGTGAGCGGGGGCTGGCTGG CCCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9890927..9891052 26863196 MeRIP-seq:(Medium) rs774444949 Functional Loss DEL dbSNP153 33..35 33 - - - 57474 RMVar_ID_57474 Human_SNP_ID_122420488 m1A Human chr3 - 9890939 9890939 9890939 ATGGGGGACAGGCCCGAAGCCGTCACGGGAGGAGGGGACTTGGCAGGTGAGCGGGGGCTGGCTGG ATGGGGGACAGGCCCGAAGCCGTCACGGGAGGGGGGGACTTGGCAGGTGAGCGGGGGCTGGCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9890927..9891052 26863196 MeRIP-seq:(Medium) rs965239782 Functional Loss SNV dbSNP153 33..33 33 - - - 57475 RMVar_ID_57475 Human_SNP_ID_122424192 m1A Human chr3 - 9902958 9902958 9902958 GGTCGATGACTATGAGGAGGAGAGGCAGGAGCAGGGCTGCCAGTCTGGAGCTCCCCATGGGCTTC GGTCGATGACTATGAGGAGGAGAGGCAGGAGCTGGGCTGCCAGTCTGGAGCTCCCCATGGGCTTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9902945..9903028 26863196 MeRIP-seq:(Medium) rs1238418797 Functional Loss SNV dbSNP153 33..33 33 - - - 57476 RMVar_ID_57476 Human_SNP_ID_122431558 m1A Human chr3 + 9928355 9928355 9928355 ACCTCTGGCAAGCCGCCCGACTGCAACTGCTGACCCTGCAGAGCTGGCTGCTGGACGCACCGTGC ACCTCTGGCAAGCCGCCCGACTGCAACTGCTGTCCCTGCAGAGCTGGCTGCTGGACGCACCGTGC A T IL17RC Ensembl:ENSG00000163702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9928236..9928445 26863196 MeRIP-seq:(Medium) rs1450817827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934746,Human_RBP_ID_9394608,Human_RBP_ID_19011435 Human_Splice_Rec_391536,Human_Splice_Rec_391566,Human_Splice_Rec_391598,Human_Splice_Rec_391614,Human_Splice_Rec_391632,Human_Splice_Rec_391652,Human_Splice_Rec_391686,Human_Splice_Rec_391718,Human_Splice_Rec_391750,Human_Splice_Rec_391782,Human_Splice_Rec_391816,Human_Splice_Rec_391852,Human_Splice_Rec_391884,Human_Splice_Rec_391926,Human_Splice_Rec_391990,Human_Splice_Rec_392024,Human_Splice_Rec_392058,Human_Splice_Rec_392070 RMVar_hsa_circ_33732 57477 RMVar_ID_57477 Human_SNP_ID_122431591 m1A Human chr3 + 9928408 9928408 9928408 GACGCACCGTGCTCGCTGCCCGCAGAAGCGGCACTGTGCTGGCGGGCTCCGGGTGGGGACCCCTG GACGCACCGTGCTCGCTGCCCGCAGAAGCGGCGCTGTGCTGGCGGGCTCCGGGTGGGGACCCCTG A G IL17RC Ensembl:ENSG00000163702 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:9928301..9928450 26863196 MeRIP-seq:(Medium) rs753009287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_391537,Human_Splice_Rec_391567,Human_Splice_Rec_391615,Human_Splice_Rec_391633,Human_Splice_Rec_391653,Human_Splice_Rec_391687,Human_Splice_Rec_391719,Human_Splice_Rec_391751,Human_Splice_Rec_391783,Human_Splice_Rec_391817,Human_Splice_Rec_391853,Human_Splice_Rec_391885,Human_Splice_Rec_391927,Human_Splice_Rec_391991,Human_Splice_Rec_392025,Human_Splice_Rec_392059,Human_Splice_Rec_392071 RMVar_hsa_circ_33732 57478 RMVar_ID_57478 Human_SNP_ID_122431592 m1A Human chr3 - 9928410 9928410 9928410 GGCAGGGGTCCCCACCCGGAGCCCGCCAGCACAGTGCCGCTTCTGCGGGCAGCGAGCACGGTGCG GGCAGGGGTCCCCACCCGGAGCCCGCCAGCACCGTGCCGCTTCTGCGGGCAGCGAGCACGGTGCG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:9928360..9928542 26863196 MeRIP-seq:(Medium) rs373390329 Functional Loss SNV dbSNP153 33..33 33 - - - 57479 RMVar_ID_57479 Human_SNP_ID_122433426 m1A Human chr3 + 9933359 9933359 9933359 TGCTTCGACAGGCTGCTCCACCCGGACGCCGTACCCGCCCTTTTCCGCACCGTGCCCGTCTTCAC TGCTTCGACAGGCTGCTCCACCCGGACGCCGTCCCCGCCCTTTTCCGCACCGTGCCCGTCTTCAC A C AC018809.3,IL17RC Ensembl:ENSG00000288550,Ensembl:ENSG00000163702 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9933030..9933381 32194978 MeRIP-seq:(Medium) rs745345902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5149625,Human_RBP_ID_27505110 57480 RMVar_ID_57480 Human_SNP_ID_122433427 m1A Human chr3 + 9933359 9933359 9933359 TGCTTCGACAGGCTGCTCCACCCGGACGCCGTACCCGCCCTTTTCCGCACCGTGCCCGTCTTCAC TGCTTCGACAGGCTGCTCCACCCGGACGCCGTGCCCGCCCTTTTCCGCACCGTGCCCGTCTTCAC A G AC018809.3,IL17RC Ensembl:ENSG00000288550,Ensembl:ENSG00000163702 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9933030..9933381 32194978 MeRIP-seq:(Medium) rs745345902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5149625,Human_RBP_ID_27505110 57481 RMVar_ID_57481 Human_SNP_ID_122433868 m1A Human chr3 - 9934398 9934398 9934398 AGGCTGGGGACCTGCAGATAGAGGGCGTGGAGAGGCTTCACTGAAGGAGTCAGGCCCCACGCGAG AGGCTGGGGACCTGCAGATAGAGGGCGTGGAGGGGCTTCACTGAAGGAGTCAGGCCCCACGCGAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:9934348..9934439 26863196 MeRIP-seq:(Medium) rs763606299 Functional Loss SNV dbSNP153 33..33 33 - - - 57482 RMVar_ID_57482 Human_SNP_ID_122433937 m1A Human chr3 - 9934547 9934547 9934547 ATGACACGGATGGGGCTGAGGCGGGGGAGAAGACTGGGGAGGTGGAGAGGGCTGGAGCCAGATAG ATGACACGGATGGGGCTGAGGCGGGGGAGAAGTCTGGGGAGGTGGAGAGGGCTGGAGCCAGATAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:9934395..9934546 26863196 MeRIP-seq:(Medium) rs1413486339 Functional Loss SNV dbSNP153 33..33 33 - - - 57483 RMVar_ID_57483 Human_SNP_ID_122436586 m1A Human chr3 + 9942859 9942859 9942859 GGCACAGAGGGAGCCAACTGTGGAGCTGACCAATTCTGCGTGAACACTGAGGGCTCCTATGAGTG GGCACAGAGGGAGCCAACTGTGGAGCTGACCAGTTCTGCGTGAACACTGAGGGCTCCTATGAGTG A G AC018809.3,CRELD1 Ensembl:ENSG00000288550,Ensembl:ENSG00000163703 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:9941202..9943217 32194978 MeRIP-seq:(Medium) rs1321368548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3964664,Human_RBP_ID_19009824,Human_RBP_ID_24025473,Human_RBP_ID_27821877 Human_Splice_Rec_392118,Human_Splice_Rec_392119,Human_Splice_Rec_392134,Human_Splice_Rec_392135,Human_Splice_Rec_392154,Human_Splice_Rec_392155,Human_Splice_Rec_392174,Human_Splice_Rec_392175,Human_Splice_Rec_392192,Human_Splice_Rec_392193,Human_Splice_Rec_392212,Human_Splice_Rec_392213,Human_Splice_Rec_392232,Human_Splice_Rec_392233,Human_Splice_Rec_392254,Human_Splice_Rec_392255,Human_Splice_Rec_392270,Human_Splice_Rec_392271,Human_Splice_Rec_392290,Human_Splice_Rec_392291,Human_Splice_Rec_392306,Human_Splice_Rec_392307,Human_Splice_Rec_392314,Human_Splice_Rec_392315,Human_Splice_Rec_392322,Human_Splice_Rec_392323,Human_Splice_Rec_392325 RMVar_hsa_circ_91630,RMVar_hsa_circ_336228,RMVar_hsa_circ_215737 57484 RMVar_ID_57484 Human_SNP_ID_122448935 m1A Human chr3 - 9986709 9986709 9986709 GGCGAAGCCGAAGAGAAGCAACTGTGCCCCGGAGAAGAGAAGCTCGCCCATTCCAGACTGGGAAC GGCGAAGCCGAAGAGAAGCAACTGTGCCCCGGGGAAGAGAAGCTCGCCCATTCCAGACTGGGAAC T C EMC3 Ensembl:ENSG00000125037 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9986661..9986785 26863196 MeRIP-seq:(Medium) rs373153918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247279,Human_RBP_ID_836323,Human_RBP_ID_1614616,Human_RBP_ID_4756980,Human_RBP_ID_9333597,Human_RBP_ID_9393291,Human_RBP_ID_18445760,Human_RBP_ID_23134611,Human_RBP_ID_27310934,Human_RBP_ID_27496219 Human_miRNA_ID_3116228 RMVar_hsa_circ_108738,RMVar_hsa_circ_215742,RMVar_hsa_circ_340033,RMVar_hsa_circ_320587,RMVar_hsa_circ_215750,RMVar_hsa_circ_338937 57485 RMVar_ID_57485 Human_SNP_ID_122448945 m1A Human chr3 - 9986731 9986731 9986731 AAGGGGCTTGAGAAGGCCCGGAGGCGAAGCCGAAGAGAAGCAACTGTGCCCCGGAGAAGAGAAGC AAGGGGCTTGAGAAGGCCCGGAGGCGAAGCCGGAGAGAAGCAACTGTGCCCCGGAGAAGAGAAGC T C EMC3 Ensembl:ENSG00000125037 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9986551..9986800 32194978 MeRIP-seq:(Medium) rs1433118899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247279,Human_RBP_ID_836323,Human_RBP_ID_4756980,Human_RBP_ID_9393291,Human_RBP_ID_18445760,Human_RBP_ID_22457217 Human_miRNA_ID_3116229 RMVar_hsa_circ_108738,RMVar_hsa_circ_215742,RMVar_hsa_circ_340033,RMVar_hsa_circ_320587,RMVar_hsa_circ_215750,RMVar_hsa_circ_338937 57486 RMVar_ID_57486 Human_SNP_ID_122459751 m1A Human chr3 - 10026266 10026266 10026266 CGGGCATAGGGGCGAGAGAAGGCCCAGAGGCGACGTCAGAGAGAAGCAACTGCGCCCCGGTGAAG CGGGCATAGGGGCGAGAGAAGGCCCAGAGGCGGCGTCAGAGAGAAGCAACTGCGCCCCGGTGAAG T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:10026216..10026331 26863196 MeRIP-seq:(Medium) rs1559366196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756981,Human_RBP_ID_10484668,Human_RBP_ID_21960450,Human_RBP_ID_27821883 57487 RMVar_ID_57487 Human_SNP_ID_122467554 m1A Human chr3 + 10051570 10051570 10051570 AAGGGTGGAAGCCAGAGAGCAGTAACTTGAAGACTTGGGGAATAGAGTCAATGTCGAGAAGCATC AAGGGTGGAAGCCAGAGAGCAGTAACTTGAAGCCTTGGGGAATAGAGTCAATGTCGAGAAGCATC A C FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:10051565..10051690 26863196 MeRIP-seq:(Medium) rs1332079837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14548874 RMVar_hsa_circ_8843,RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_215756,RMVar_hsa_circ_114606,RMVar_hsa_circ_104365,RMVar_hsa_circ_215757,RMVar_hsa_circ_215759,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_77614,RMVar_hsa_circ_215763,RMVar_hsa_circ_120008,RMVar_hsa_circ_99141,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215765,RMVar_hsa_circ_45778,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_72165,RMVar_hsa_circ_124318,RMVar_hsa_circ_122156,RMVar_hsa_circ_215771,RMVar_hsa_circ_277918,RMVar_hsa_circ_215772,RMVar_hsa_circ_311631,RMVar_hsa_circ_86339,RMVar_hsa_circ_92781,RMVar_hsa_circ_75780,RMVar_hsa_circ_215775,RMVar_hsa_circ_215777,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,RMVar_hsa_circ_215776,RMVar_hsa_circ_85392,RMVar_hsa_circ_127890,RMVar_hsa_circ_77302,RMVar_hsa_circ_215780,RMVar_hsa_circ_215781,RMVar_hsa_circ_265956,RMVar_hsa_circ_215782 57488 RMVar_ID_57488 Human_SNP_ID_122470027 m1A Human chr3 + 10059822 10059822 10059822 AGCGAGACTCCTTCTCAAAGAAAAAAAAAAAAAGTCCCCATTTCACAGATGTAAAAATTAAAACT AGCGAGACTCCTTCTCAAAGAAAAAAAAAAAAGGTCCCCATTTCACAGATGTAAAAATTAAAACT A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:10059737..10059824 26863410 MeRIP-seq:(Medium) rs74882077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8843,RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_215756,RMVar_hsa_circ_114606,RMVar_hsa_circ_104365,RMVar_hsa_circ_215757,RMVar_hsa_circ_215759,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_77614,RMVar_hsa_circ_215763,RMVar_hsa_circ_120008,RMVar_hsa_circ_99141,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215765,RMVar_hsa_circ_45778,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_20779,RMVar_hsa_circ_72165,RMVar_hsa_circ_124318,RMVar_hsa_circ_122156,RMVar_hsa_circ_215771,RMVar_hsa_circ_277918,RMVar_hsa_circ_215772,RMVar_hsa_circ_86339,RMVar_hsa_circ_92781,RMVar_hsa_circ_75780,RMVar_hsa_circ_215775,RMVar_hsa_circ_215777,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,RMVar_hsa_circ_215776,RMVar_hsa_circ_85392,RMVar_hsa_circ_127890,RMVar_hsa_circ_77302,RMVar_hsa_circ_215780,RMVar_hsa_circ_215781,RMVar_hsa_circ_265956,RMVar_hsa_circ_314439,RMVar_hsa_circ_215782,RMVar_hsa_circ_94327,RMVar_hsa_circ_215783,RMVar_hsa_circ_215784 57489 RMVar_ID_57489 Human_SNP_ID_122470028 m1A Human chr3 + 10059822 10059822 10059822 AGCGAGACTCCTTCTCAAAGAAAAAAAAAAAAAGTCCCCATTTCACAGATGTAAAAATTAAAACT AGCGAGACTCCTTCTCAAAGAAAAAAAAAAAATGTCCCCATTTCACAGATGTAAAAATTAAAACT A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:10059737..10059824 26863410 MeRIP-seq:(Medium) rs74882077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8843,RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_215756,RMVar_hsa_circ_114606,RMVar_hsa_circ_104365,RMVar_hsa_circ_215757,RMVar_hsa_circ_215759,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_77614,RMVar_hsa_circ_215763,RMVar_hsa_circ_120008,RMVar_hsa_circ_99141,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215765,RMVar_hsa_circ_45778,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_20779,RMVar_hsa_circ_72165,RMVar_hsa_circ_124318,RMVar_hsa_circ_122156,RMVar_hsa_circ_215771,RMVar_hsa_circ_277918,RMVar_hsa_circ_215772,RMVar_hsa_circ_86339,RMVar_hsa_circ_92781,RMVar_hsa_circ_75780,RMVar_hsa_circ_215775,RMVar_hsa_circ_215777,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,RMVar_hsa_circ_215776,RMVar_hsa_circ_85392,RMVar_hsa_circ_127890,RMVar_hsa_circ_77302,RMVar_hsa_circ_215780,RMVar_hsa_circ_215781,RMVar_hsa_circ_265956,RMVar_hsa_circ_314439,RMVar_hsa_circ_215782,RMVar_hsa_circ_94327,RMVar_hsa_circ_215783,RMVar_hsa_circ_215784 57490 RMVar_ID_57490 Human_SNP_ID_122481447 m1A Human chr3 + 10101155 10101154 10101155 TGTATTCCAGAGGTCACCCAGAGCAGTAACCTAAAATGCTTATTTATTTATTCTTTGCCCCTTAG TGTATTCCAGAGGTCACCCAGAGCAGTAACCT_AAATGCTTATTTATTTATTCTTTGCCCCTTAG TA T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10101152..10101289 26863196 MeRIP-seq:(Medium) rs759927900 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_215779,RMVar_hsa_circ_127890,RMVar_hsa_circ_215781,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_215783,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_93917,RMVar_hsa_circ_215795,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_103351,RMVar_hsa_circ_215815,RMVar_hsa_circ_95112,RMVar_hsa_circ_215816,RMVar_hsa_circ_215817,RMVar_hsa_circ_90637 57491 RMVar_ID_57491 Human_SNP_ID_122493289 m1A Human chr3 - 10141906 10141906 10141906 CCCCGCCGTCTTCTTCAGGGCCGTACTCTTCGACGCCTGCCTCCTCCGCGCCTACCTCGGCCTCG CCCCGCCGTCTTCTTCAGGGCCGTACTCTTCGGCGCCTGCCTCCTCCGCGCCTACCTCGGCCTCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:10141824..10142100 26863196 MeRIP-seq:(Medium) rs929332564 Functional Loss SNV dbSNP153 33..33 33 - - - 57492 RMVar_ID_57492 Human_SNP_ID_122493291 m1A Human chr3 + 10141909 10141909 10141909 GGCCGAGGTAGGCGCGGAGGAGGCAGGCGTCGAAGAGTACGGCCCTGAAGAAGACGGCGGGGAGG GGCCGAGGTAGGCGCGGAGGAGGCAGGCGTCGCAGAGTACGGCCCTGAAGAAGACGGCGGGGAGG A C VHL Ensembl:ENSG00000134086 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr3:10141776..10142050;chr3:10141776..10142148 26863196 MeRIP-seq:(Medium) rs1060503548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4715652,Human_RBP_ID_8943457,Human_RBP_ID_9393295,Human_RBP_ID_14554131,Human_RBP_ID_23026311,Human_RBP_ID_23119954,Human_RBP_ID_26346476 Clinvar_Rec_165 57493 RMVar_ID_57493 Human_SNP_ID_122497025 m1A Human chr3 + 10152189 10152189 10152189 CAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCATTTCTACTAAAAAATACAAGAATT CAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATTTCTACTAAAAAATACAAGAATT A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs886057734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17990414,Human_RBP_ID_27709790 Clinvar_Rec_30,Clinvar_Rec_166 57494 RMVar_ID_57494 Human_SNP_ID_122497310 m1A Human chr3 + 10153057 10153057 10153057 CCAGCACTTTGGGAGGCCTAGGCGGGTGGATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAA CCAGCACTTTGGGAGGCCTAGGCGGGTGGATCGCGAGGTCAGGAAATCGAGACCATCCTGGCTAA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1026556299 Functional Loss SNV dbSNP153 33..33 33 - - - 57495 RMVar_ID_57495 Human_SNP_ID_122497345 m1A Human chr3 + 10153167 10153167 10153167 GGGCGTGGTGGTGAGCGCCTGTAGTCCCAGCTACTCGAGAGCCTGAGGCAGGAGAATGGCATGAA GGGCGTGGTGGTGAGCGCCTGTAGTCCCAGCTGCTCGAGAGCCTGAGGCAGGAGAATGGCATGAA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1362807922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584677,Human_RBP_ID_14554632,Human_RBP_ID_23312185 57496 RMVar_ID_57496 Human_SNP_ID_122497426 m1A Human chr3 + 10153378 10153378 10153378 TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAAC TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAAC A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1136250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10113896,Human_RBP_ID_25765459 57497 RMVar_ID_57497 Human_SNP_ID_122524486 m1A Human chr3 + 10248649 10248649 10248649 GGCGTCCTGAGTTGGCGGTCGAGGGCGCTGCCAGCTCCCGAGGGGCCGCTCGGGCCCCTTCCGGC GGCGTCCTGAGTTGGCGGTCGAGGGCGCTGCCCGCTCCCGAGGGGCCGCTCGGGCCCCTTCCGGC A C TATDN2 Ensembl:ENSG00000157014 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:10248548..10248793 26863410 MeRIP-seq:(Medium) rs1218882255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247464,Human_RBP_ID_4715838,Human_RBP_ID_5530184 RMVar_hsa_circ_215827,RMVar_hsa_circ_101231 57498 RMVar_ID_57498 Human_SNP_ID_122524743 m1A Human chr3 + 10249306 10249306 10249306 GCCTCCGGGAGCCCTGTGATGTGGCCCCCTCCAGCCGGCCAGCTCAGAGGTCTGCGTCGCGTTCT GCCTCCGGGAGCCCTGTGATGTGGCCCCCTCCTGCCGGCCAGCTCAGAGGTCTGCGTCGCGTTCT A T TATDN2 Ensembl:ENSG00000157014 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:10249256..10249358 26863196 MeRIP-seq:(Medium) rs953317829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530796,Human_RBP_ID_8874812 RMVar_hsa_circ_215827,RMVar_hsa_circ_101231 57499 RMVar_ID_57499 Human_SNP_ID_122524809 m1A Human chr3 - 10249438 10249436 10249439 GCCCAAGAAATGTGGGGAGAAGGAGGAGGAGGAGTTATTTCTGCGGCGGGATGAGCCCCAGGATA GCCCAAGAAATGTGGGGAGAAGGAGGAGGAG___TTATTTCTGCGGCGGGATGAGCCCCAGGATA ACTC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:10249017..10249443 32194978 MeRIP-seq:(Medium) rs751012309 Functional Loss DEL dbSNP153 32..34 33 - - - 57500 RMVar_ID_57500 Human_SNP_ID_122524812 m1A Human chr3 - 10249438 10249438 10249438 GCCCAAGAAATGTGGGGAGAAGGAGGAGGAGGAGTTATTTCTGCGGCGGGATGAGCCCCAGGATA GCCCAAGAAATGTGGGGAGAAGGAGGAGGAGGTGTTATTTCTGCGGCGGGATGAGCCCCAGGATA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:10249017..10249443 32194978 MeRIP-seq:(Medium) rs770435769 Functional Loss SNV dbSNP153 33..33 33 - - - 57501 RMVar_ID_57501 Human_SNP_ID_122528113 m1A Human chr3 + 10260494 10260494 10260494 AGAAGGAGAAAGACGCAACCCCAGAGGTCAGCATGGAGGAGGATAAGACAGTGCCAGAGAGGAGC AGAAGGAGAAAGACGCAACCCCAGAGGTCAGCGTGGAGGAGGATAAGACAGTGCCAGAGAGGAGC A G TATDN2,AC022384.1 Ensembl:ENSG00000157014,Ensembl:ENSG00000272410 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10260261..10260529 26863196 MeRIP-seq:(Medium) rs761566077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530193,Human_RBP_ID_9393299,Human_RBP_ID_26346480,Human_RBP_ID_27565551 Human_miRNA_ID_957056,Human_miRNA_ID_957057,Human_miRNA_ID_2896131,Human_miRNA_ID_2948489 RMVar_hsa_circ_215827,RMVar_hsa_circ_101231,RMVar_hsa_circ_291127,RMVar_hsa_circ_356849 57502 RMVar_ID_57502 Human_SNP_ID_122533657 m1A Human chr3 - 10280870 10280868 10280871 GGCACTACTGACTTCAGGGCTTGCTGGAGAGGAGATGGTTGTGCTGCAGTTCACTTGGTGACTAT GGCACTACTGACTTCAGGGCTTGCTGGAGAG___ATGGTTGTGCTGCAGTTCACTTGGTGACTAT TCTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10280820..10280921 26863196 MeRIP-seq:(Medium) rs1195112302 Functional Loss DEL dbSNP153 32..34 33 - - - 57503 RMVar_ID_57503 Human_SNP_ID_122533659 m1A Human chr3 - 10280870 10280870 10280870 GGCACTACTGACTTCAGGGCTTGCTGGAGAGGAGATGGTTGTGCTGCAGTTCACTTGGTGACTAT GGCACTACTGACTTCAGGGCTTGCTGGAGAGGTGATGGTTGTGCTGCAGTTCACTTGGTGACTAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10280820..10280921 26863196 MeRIP-seq:(Medium) rs1044457161 Functional Loss SNV dbSNP153 33..33 33 - - - 57504 RMVar_ID_57504 Human_SNP_ID_122539803 m1A Human chr3 - 10301268 10301268 10301268 ATCAGCATCAGTGACAGAGGGCCAGCAGAACGAGCAGTGACAAGACAGGTGGGGCCTGGCTCCCC ATCAGCATCAGTGACAGAGGGCCAGCAGAACGGGCAGTGACAAGACAGGTGGGGCCTGGCTCCCC T C SEC13 Ensembl:ENSG00000157020 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10301219..10301408 26863196 MeRIP-seq:(Medium) rs1184527547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155340,Human_RBP_ID_247473,Human_RBP_ID_1615183,Human_RBP_ID_5120199,Human_RBP_ID_5601785,Human_RBP_ID_7099980,Human_RBP_ID_14555777,Human_RBP_ID_17404497,Human_RBP_ID_17661335,Human_RBP_ID_18013685,Human_RBP_ID_22457221,Human_RBP_ID_23957012 RMVar_hsa_circ_215832,RMVar_hsa_circ_93948,RMVar_hsa_circ_118440,RMVar_hsa_circ_126046,RMVar_hsa_circ_114023,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_215830,RMVar_hsa_circ_215831 57505 RMVar_ID_57505 Human_SNP_ID_122541046 m1A Human chr3 - 10305145 10305125 10305146 TCTTTCTGTCCCCACTGTTAGGGAGGAGGAGGACGGCCAGTGGAAGGAGGAGCAGAAGCTAGAAG TCTTTCTGTCCCCACTGTTAGGGAGGAGGAG_____________________CAGAAGCTAGAAG GCTCCTCCTTCCACTGGCCGTC G SEC13 Ensembl:ENSG00000157020 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10305000..10305199 26863196 MeRIP-seq:(Medium) rs1257615659 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_783548,Human_RBP_ID_3964706,Human_RBP_ID_4716064,Human_RBP_ID_18194472,Human_RBP_ID_22456476,Human_RBP_ID_22675985,Human_RBP_ID_23026315 Human_Splice_Rec_393108,Human_Splice_Rec_393126,Human_Splice_Rec_393142,Human_Splice_Rec_393152,Human_Splice_Rec_393168,Human_Splice_Rec_393186,Human_Splice_Rec_393200,Human_Splice_Rec_393204 Human_miRNA_ID_2155113,Human_miRNA_ID_2158674,Human_miRNA_ID_2967682 RMVar_hsa_circ_25247,RMVar_hsa_circ_215832,RMVar_hsa_circ_118440,RMVar_hsa_circ_114023,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_278113,RMVar_hsa_circ_321863,RMVar_hsa_circ_127072,RMVar_hsa_circ_215835,RMVar_hsa_circ_215836 57506 RMVar_ID_57506 Human_SNP_ID_122541057 m1A Human chr3 - 10305145 10305145 10305145 TCTTTCTGTCCCCACTGTTAGGGAGGAGGAGGACGGCCAGTGGAAGGAGGAGCAGAAGCTAGAAG TCTTTCTGTCCCCACTGTTAGGGAGGAGGAGGGCGGCCAGTGGAAGGAGGAGCAGAAGCTAGAAG T C SEC13 Ensembl:ENSG00000157020 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10305000..10305199 26863196 MeRIP-seq:(Medium) rs1191333841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783548,Human_RBP_ID_3964706,Human_RBP_ID_4716064,Human_RBP_ID_18194472,Human_RBP_ID_22456476,Human_RBP_ID_22675985,Human_RBP_ID_23026315 Human_Splice_Rec_393108,Human_Splice_Rec_393126,Human_Splice_Rec_393142,Human_Splice_Rec_393152,Human_Splice_Rec_393168,Human_Splice_Rec_393186,Human_Splice_Rec_393200,Human_Splice_Rec_393204 Human_miRNA_ID_2155113,Human_miRNA_ID_2158674,Human_miRNA_ID_2967682 RMVar_hsa_circ_25247,RMVar_hsa_circ_215832,RMVar_hsa_circ_118440,RMVar_hsa_circ_114023,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_278113,RMVar_hsa_circ_321863,RMVar_hsa_circ_127072,RMVar_hsa_circ_215835,RMVar_hsa_circ_215836 57507 RMVar_ID_57507 Human_SNP_ID_122543933 m1A Human chr3 - 10315372 10315372 10315372 CCTGGCAACCTGCTCATCAGACAGGTCCGTCAAAATCTTTGATGTGCGCAATGGAGGGCAGATCC CCTGGCAACCTGCTCATCAGACAGGTCCGTCAGAATCTTTGATGTGCGCAATGGAGGGCAGATCC T C SEC13 Ensembl:ENSG00000157020 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10315276..10315480 26863196 MeRIP-seq:(Medium) rs906510801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1615201,Human_RBP_ID_1945693,Human_RBP_ID_8554441,Human_RBP_ID_22457229,Human_RBP_ID_27042308 Human_Splice_Rec_393100,Human_Splice_Rec_393101,Human_Splice_Rec_393118,Human_Splice_Rec_393119,Human_Splice_Rec_393134,Human_Splice_Rec_393135,Human_Splice_Rec_393160,Human_Splice_Rec_393161,Human_Splice_Rec_393178,Human_Splice_Rec_393179,Human_Splice_Rec_393192,Human_Splice_Rec_393193,Human_Splice_Rec_393214,Human_Splice_Rec_393215,Human_Splice_Rec_393224,Human_Splice_Rec_393225,Human_Splice_Rec_393230,Human_Splice_Rec_393231,Human_Splice_Rec_393236,Human_Splice_Rec_393242 Human_miRNA_ID_2046710 RMVar_hsa_circ_118440,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_127072,RMVar_hsa_circ_215836 57508 RMVar_ID_57508 Human_SNP_ID_122543934 m1A Human chr3 - 10315372 10315372 10315372 CCTGGCAACCTGCTCATCAGACAGGTCCGTCAAAATCTTTGATGTGCGCAATGGAGGGCAGATCC CCTGGCAACCTGCTCATCAGACAGGTCCGTCACAATCTTTGATGTGCGCAATGGAGGGCAGATCC T G SEC13 Ensembl:ENSG00000157020 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:10315276..10315480 26863196 MeRIP-seq:(Medium) rs906510801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1615201,Human_RBP_ID_1945693,Human_RBP_ID_8554441,Human_RBP_ID_22457229,Human_RBP_ID_27042308 Human_Splice_Rec_393100,Human_Splice_Rec_393101,Human_Splice_Rec_393118,Human_Splice_Rec_393119,Human_Splice_Rec_393134,Human_Splice_Rec_393135,Human_Splice_Rec_393160,Human_Splice_Rec_393161,Human_Splice_Rec_393178,Human_Splice_Rec_393179,Human_Splice_Rec_393192,Human_Splice_Rec_393193,Human_Splice_Rec_393214,Human_Splice_Rec_393215,Human_Splice_Rec_393224,Human_Splice_Rec_393225,Human_Splice_Rec_393230,Human_Splice_Rec_393231,Human_Splice_Rec_393236,Human_Splice_Rec_393242 Human_miRNA_ID_2046710 RMVar_hsa_circ_118440,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_127072,RMVar_hsa_circ_215836 57509 RMVar_ID_57509 Human_SNP_ID_122766689 m1A Human chr3 - 11213051 11213051 11213051 AGTGATGGCTGAAGTGGGTCTGCTGTTTATATAGGGTGGTCAAGGTGATCTGGCAACATTTGAGC AGTGATGGCTGAAGTGGGTCTGCTGTTTATATCGGGTGGTCAAGGTGATCTGGCAACATTTGAGC T G AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:11212927..11213088 26863196 MeRIP-seq:(Medium) rs879113957 Functional Loss SNV dbSNP153 33..33 33 - - - 57510 RMVar_ID_57510 Human_SNP_ID_122769982 m1A Human chr3 + 11225803 11225803 11225803 TGCCTCCCGGGTTCAGGCGACTCACATGCCTCAGTCTCCCAAGTGCTGGGATTACAGGCATGAGC TGCCTCCCGGGTTCAGGCGACTCACATGCCTCTGTCTCCCAAGTGCTGGGATTACAGGCATGAGC A T HRH1 Ensembl:ENSG00000196639 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:11225761..11225844 26863196 MeRIP-seq:(Medium) rs1370171404 Functional Loss SNV dbSNP153 33..33 33 - - - 57511 RMVar_ID_57511 Human_SNP_ID_122769985 m1A Human chr3 - 11225817 11225817 11225817 GGTCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTGGGAGACTGAGGCATGTGAGTCGCCT GGTCGGGTGCGGTGGCTCATGCCTGTAATCCCGGCACTTGGGAGACTGAGGCATGTGAGTCGCCT T C AC083855.2 Ensembl:ENSG00000285906 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:11225778..11225904 26863196 MeRIP-seq:(Medium) rs1056316876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8555073 57512 RMVar_ID_57512 Human_SNP_ID_122802665 m1A Human chr3 - 11358545 11358545 11358545 ACCGGCTCTCCCTGGTGTCCATCAATAGGAAGACGACATCATGGCTTTCGATGAGCTGCTCCAGT ACCGGCTCTCCCTGGTGTCCATCAATAGGAAGGCGACATCATGGCTTTCGATGAGCTGCTCCAGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:11358502..11360621 32194978 MeRIP-seq:(Medium) rs36117895 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_6727,GWAS_ID_6728,GWAS_ID_6729,GWAS_ID_6730 57513 RMVar_ID_57513 Human_SNP_ID_122820669 m1A Human chr3 + 11426896 11426896 11426896 CATTCCTTCTTAGAAGACTTGACTGGTCTTACATTGCTGCATCAAGAAACCCAAGCTGCTGAGGT CATTCCTTCTTAGAAGACTTGACTGGTCTTACCTTGCTGCATCAAGAAACCCAAGCTGCTGAGGT A C ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:11426845..11446527 32194978 MeRIP-seq:(Medium) rs1397463445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69448 Human_Splice_Rec_394908,Human_Splice_Rec_394909,Human_Splice_Rec_394944,Human_Splice_Rec_394945,Human_Splice_Rec_395022,Human_Splice_Rec_395023,Human_Splice_Rec_395028,Human_Splice_Rec_395029,Human_Splice_Rec_395034,Human_Splice_Rec_395035 RMVar_hsa_circ_110,RMVar_hsa_circ_373095,RMVar_hsa_circ_215854,RMVar_hsa_circ_324359,RMVar_hsa_circ_304093,RMVar_hsa_circ_215872,RMVar_hsa_circ_303724,RMVar_hsa_circ_349649,RMVar_hsa_circ_215873,RMVar_hsa_circ_282809,RMVar_hsa_circ_215884,RMVar_hsa_circ_317877,RMVar_hsa_circ_215891,RMVar_hsa_circ_115042,RMVar_hsa_circ_215893,RMVar_hsa_circ_108562,RMVar_hsa_circ_277160,RMVar_hsa_circ_215894,RMVar_hsa_circ_215895,RMVar_hsa_circ_4543,RMVar_hsa_circ_8831,RMVar_hsa_circ_215904,RMVar_hsa_circ_318163,RMVar_hsa_circ_215903 57514 RMVar_ID_57514 Human_SNP_ID_122856931 m1A Human chr3 - 11556351 11556351 11556351 CCGGGTCCCTGGTGCACTGACCTATCTGGGATAGGCAGTACCCTGGAGGGGGGCCTGGGGCAGAG CCGGGTCCCTGGTGCACTGACCTATCTGGGATGGGCAGTACCCTGGAGGGGGGCCTGGGGCAGAG T C VGLL4 Ensembl:ENSG00000144560 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:11556217..11556467 32194978 MeRIP-seq:(Medium) rs1371248449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_586351,Human_RBP_ID_1102453,Human_RBP_ID_18794266 57515 RMVar_ID_57515 Human_SNP_ID_122857754 m1A Human chr3 - 11558594 11558594 11558594 GCAGGGGCCAGCCCGCCAGCCCCTCTGCCCACATGGTCAGCCACAGTCACTCCCCCTCTGTGGTC GCAGGGGCCAGCCCGCCAGCCCCTCTGCCCACGTGGTCAGCCACAGTCACTCCCCCTCTGTGGTC T C VGLL4 Ensembl:ENSG00000144560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:11558545..11558649;chr3:11558544..11558620 26863196 MeRIP-seq:(Medium) rs756315421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_586391,Human_RBP_ID_9394633 Human_miRNA_ID_251673,Human_miRNA_ID_820831 57516 RMVar_ID_57516 Human_SNP_ID_122858330 m1A Human chr3 - 11560093 11560093 11560093 AGAGAGAGATCTGAACAGGGCTTGAAGGAACAAGGGGAGTTTGCCAGGCAGACAGCGTGGGGGTG AGAGAGAGATCTGAACAGGGCTTGAAGGAACACGGGGAGTTTGCCAGGCAGACAGCGTGGGGGTG T G VGLL4 Ensembl:ENSG00000144560 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:11560076..11560168 26863196 MeRIP-seq:(Medium) rs17034656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93656,RMVar_hsa_circ_215906 57517 RMVar_ID_57517 Human_SNP_ID_122859920 m1A Human chr3 - 11564978 11564978 11564978 TGCCAATGGAGACTGCCGCAGAGACCCCCGGGAGCGGAGCCGCAGCCCCATCGAGCGCGCTGTGG TGCCAATGGAGACTGCCGCAGAGACCCCCGGGCGCGGAGCCGCAGCCCCATCGAGCGCGCTGTGG T G VGLL4 Ensembl:ENSG00000144560 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:11564951..11565025 26863196 MeRIP-seq:(Medium) rs1259758354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933584,Human_RBP_ID_19011493 Human_Splice_Rec_395040,Human_Splice_Rec_395050,Human_Splice_Rec_395058,Human_Splice_Rec_395064,Human_Splice_Rec_395070,Human_Splice_Rec_395082,Human_Splice_Rec_395092,Human_Splice_Rec_395102,Human_Splice_Rec_395110,Human_Splice_Rec_395118,Human_Splice_Rec_395128,Human_Splice_Rec_395132,Human_Splice_Rec_395138,Human_Splice_Rec_395142 RMVar_hsa_circ_93656,RMVar_hsa_circ_215906 57518 RMVar_ID_57518 Human_SNP_ID_122870131 m1A Human chr3 + 11601796 11601796 11601796 AAAGTTGCAAAACAAATAAGGCCCCAGCACGGAGCACCCTTAAGCCAAAATAAGAACAGAGGAAC AAAGTTGCAAAACAAATAAGGCCCCAGCACGGGGCACCCTTAAGCCAAAATAAGAACAGAGGAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:11601791..11601856 26863196 MeRIP-seq:(Medium) rs1286624136 Functional Loss SNV dbSNP153 33..33 33 - - - 57519 RMVar_ID_57519 Human_SNP_ID_122870132 m1A Human chr3 + 11601796 11601796 11601796 AAAGTTGCAAAACAAATAAGGCCCCAGCACGGAGCACCCTTAAGCCAAAATAAGAACAGAGGAAC AAAGTTGCAAAACAAATAAGGCCCCAGCACGGTGCACCCTTAAGCCAAAATAAGAACAGAGGAAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:11601791..11601856 26863196 MeRIP-seq:(Medium) rs1286624136 Functional Loss SNV dbSNP153 33..33 33 - - - 57520 RMVar_ID_57520 Human_SNP_ID_122870169 m1A Human chr3 + 11601880 11601880 11601880 ATGCGACTCATTTTGGAGACGTGGTCGTTGTCACAGTCTAGGTCCTCGTCACCTGGCTCCATGCT ATGCGACTCATTTTGGAGACGTGGTCGTTGTCGCAGTCTAGGTCCTCGTCACCTGGCTCCATGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:11601781..11601908 26863196 MeRIP-seq:(Medium) rs143577475 Functional Loss SNV dbSNP153 33..33 33 - - - 57521 RMVar_ID_57521 Human_SNP_ID_122878136 m1A Human chr3 - 11633330 11633330 11633330 AGGTGTTTGTATTTTCATGGCATGCTGTGCATACTTCTGCCATGGAATTTATCTCGCTGTGTTAC AGGTGTTTGTATTTTCATGGCATGCTGTGCATTCTTCTGCCATGGAATTTATCTCGCTGTGTTAC T A VGLL4 Ensembl:ENSG00000144560 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:11633304..11633389 26863410 MeRIP-seq:(Medium) rs1015965513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215908,RMVar_hsa_circ_93656,RMVar_hsa_circ_215906,RMVar_hsa_circ_273847 57522 RMVar_ID_57522 Human_SNP_ID_122886732 m1A Human chr3 - 11666861 11666861 11666861 CATGCACACCGGAGTGGAGGGGAGCACAGAGGAGGGTTGTAGCATTCATGTTTTGTAAGTAACTA CATGCACACCGGAGTGGAGGGGAGCACAGAGGGGGGTTGTAGCATTCATGTTTTGTAAGTAACTA T C VGLL4 Ensembl:ENSG00000144560 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:11666859..11667014 26863196 MeRIP-seq:(Medium) rs531817976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215908,RMVar_hsa_circ_93656,RMVar_hsa_circ_215906,RMVar_hsa_circ_273847 57523 RMVar_ID_57523 Human_SNP_ID_122899956 m1A Human chr3 + 11719348 11719348 11719348 GGCATCCCGGTTCTGCTCCGACAGCCCACCCCAAGGCCCCTCTCAGGCCAGCCCTCGCCCAGCCC GGCATCCCGGTTCTGCTCCGACAGCCCACCCCGAGGCCCCTCTCAGGCCAGCCCTCGCCCAGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:11719341..11719422 26863196 MeRIP-seq:(Medium) rs1200438668 Functional Loss SNV dbSNP153 33..33 33 - - - 57524 RMVar_ID_57524 Human_SNP_ID_122900039 m1A Human chr3 + 11719530 11719530 11719530 GCGGGGCGCACCCCGAGGGCGCGCAGACGCACAGGCGGGCTCGCGCCCGAGCCCCCGCACGGGCC GCGGGGCGCACCCCGAGGGCGCGCAGACGCACCGGCGGGCTCGCGCCCGAGCCCCCGCACGGGCC A C lnc-ATG7-2,lnc-ATG7-2:2 RNACentral:URS00008BE584,RNACentral:URS00009B02E3 lincRNA,lincRNA exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:11719495..11719621 26863410 MeRIP-seq:(Medium) rs999579626 Functional Loss SNV dbSNP153 33..33 33 - - - 57525 RMVar_ID_57525 Human_SNP_ID_122932084 m1A Human chr3 - 11844117 11844115 11844117 GAAGAAAAATTGGAGTCACTACTCTTTCCTAAAAGTTTTAGGGCCCAAGATTATCACGTCCATCC GAAGAAAAATTGGAGTCACTACTCTTTCCTAA__GTTTTAGGGCCCAAGATTATCACGTCCATCC CTT C TAMM41 Ensembl:ENSG00000144559 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:11844049..11844249 26863196 MeRIP-seq:(Medium) rs1559334438 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1030463,Human_RBP_ID_18794433 Human_Splice_Rec_395168,Human_Splice_Rec_395169,Human_Splice_Rec_395182,Human_Splice_Rec_395183,Human_Splice_Rec_395194,Human_Splice_Rec_395195,Human_Splice_Rec_395224,Human_Splice_Rec_395225,Human_Splice_Rec_395240,Human_Splice_Rec_395241,Human_Splice_Rec_395252,Human_Splice_Rec_395253,Human_Splice_Rec_395258 RMVar_hsa_circ_79069,RMVar_hsa_circ_101250,RMVar_hsa_circ_215911,RMVar_hsa_circ_215913,RMVar_hsa_circ_30734,RMVar_hsa_circ_377173,RMVar_hsa_circ_266544 57526 RMVar_ID_57526 Human_SNP_ID_122932103 m1A Human chr3 + 11844171 11844171 11844171 AATTTTTCTTCAGGTTCTTTGAATGCCATGCGACAGGGTCATCTACTGTGAACACAAAGTCCAGC AATTTTTCTTCAGGTTCTTTGAATGCCATGCGGCAGGGTCATCTACTGTGAACACAAAGTCCAGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:11844087..11844188 26863410 MeRIP-seq:(Medium) rs777805813 Functional Loss SNV dbSNP153 33..33 33 - - - 57527 RMVar_ID_57527 Human_SNP_ID_123088748 m1A Human chr3 - 12484519 12484514 12484519 AAAGGGCCGCGCTTTCCTCGCCCAGGGCCCTTACCTTTCTTGGCCCCACGCGCTCGCCGTTACCC AAAGGGCCGCGCTTTCCTCGCCCAGGGCCCTT_____TCTTGGCCCCACGCGCTCGCCGTTACCC AAAGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:12484500..12484732;chr3:12484507..12484683 26863196 MeRIP-seq:(Medium) rs1460301457 Functional Loss DEL dbSNP153 33..37 33 - - - 57528 RMVar_ID_57528 Human_SNP_ID_123088859 m1A Human chr3 + 12484807 12484807 12484807 CTGGTGGGGCTGGGGCGCAAGGTGCAGCTGACAATGCCCGAGAGGAGCCGCAGCCTCTGGTGGAG CTGGTGGGGCTGGGGCGCAAGGTGCAGCTGACCATGCCCGAGAGGAGCCGCAGCCTCTGGTGGAG A C TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:12484803..12484870 26863196 MeRIP-seq:(Medium) rs866706372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_395699,Human_Splice_Rec_395743,Human_Splice_Rec_395759 57529 RMVar_ID_57529 Human_SNP_ID_123088860 m1A Human chr3 + 12484807 12484807 12484807 CTGGTGGGGCTGGGGCGCAAGGTGCAGCTGACAATGCCCGAGAGGAGCCGCAGCCTCTGGTGGAG CTGGTGGGGCTGGGGCGCAAGGTGCAGCTGACGATGCCCGAGAGGAGCCGCAGCCTCTGGTGGAG A G TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:12484803..12484870 26863196 MeRIP-seq:(Medium) rs866706372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_395699,Human_Splice_Rec_395743,Human_Splice_Rec_395759 57530 RMVar_ID_57530 Human_SNP_ID_123103694 m1A Human chr3 + 12539189 12539189 12539189 GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCAATGCTGCGATCTTGGATCACTGCAACCTCTGC GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCGATGCTGCGATCTTGGATCACTGCAACCTCTGC A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs113368836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9131581 Human_Splice_Rec_395778,Human_Splice_Rec_395808 GWAS_ID_110,GWAS_ID_111,GWAS_ID_112,GWAS_ID_113 RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 57531 RMVar_ID_57531 Human_SNP_ID_123108883 m1A Human chr3 + 12557139 12557139 12557139 TGCGAGAGGCGGCGGCACGACGACGGTCCCTCAGCCCAGCCACCATGAGCACCAAGCAGATCACT TGCGAGAGGCGGCGGCACGACGACGGTCCCTCGGCCCAGCCACCATGAGCACCAAGCAGATCACT A G MKRN2 Ensembl:ENSG00000075975 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12557091..12557206 26863196 MeRIP-seq:(Medium) rs1274241359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1948273,Human_RBP_ID_4719997,Human_RBP_ID_19115055 Human_Splice_Rec_395835,Human_Splice_Rec_395847,Human_Splice_Rec_395859 RMVar_hsa_circ_117010,RMVar_hsa_circ_120833,RMVar_hsa_circ_215977,RMVar_hsa_circ_100505,RMVar_hsa_circ_215978,RMVar_hsa_circ_215976 57532 RMVar_ID_57532 Human_SNP_ID_123116377 m1A Human chr3 - 12584136 12584136 12584136 GGTAGCAGGCAGTCCAGCCCTGATGTGGAGACACATGGGATTTTGGAAATCAGCTTCTGGAGGAA GGTAGCAGGCAGTCCAGCCCTGATGTGGAGACGCATGGGATTTTGGAAATCAGCTTCTGGAGGAA T C RAF1 Ensembl:ENSG00000132155 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12584086..12584162 26863196 MeRIP-seq:(Medium) rs926124509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7116316,Human_RBP_ID_26510061 RMVar_hsa_circ_85505,RMVar_hsa_circ_215984 57533 RMVar_ID_57533 Human_SNP_ID_123116566 m1A Human chr3 + 12584627 12584627 12584627 CTCGGAAGCGCTCCGGTTGATCTTCGGTAGAGAGTGTTGGAGCAGCTCAATGGAAGACAGGATCT CTCGGAAGCGCTCCGGTTGATCTTCGGTAGAGTGTGTTGGAGCAGCTCAATGGAAGACAGGATCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:12584576..12584650 32194978 MeRIP-seq:(Medium) rs1448392469 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6731 57534 RMVar_ID_57534 Human_SNP_ID_123116696 m1A Human chr3 + 12584977 12584977 12584977 CTGGGGAGGCATATCCTCGGCCCACCATGAAGATGATCTAAGGGAAAGAAAACAGCTGAGCTAAT CTGGGGAGGCATATCCTCGGCCCACCATGAAGGTGATCTAAGGGAAAGAAAACAGCTGAGCTAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:12584938..12585706 32194978 MeRIP-seq:(Medium) rs1559399152 Functional Loss SNV dbSNP153 33..33 33 - - - 57535 RMVar_ID_57535 Human_SNP_ID_123121740 m1A Human chr3 - 12603486 12603486 12603486 CTCCCAGGGCGTGGTCCAGACGATTTTGTTTGAGGGGAAGAGTAGGTATTTTTCTTCATGCCTTT CTCCCAGGGCGTGGTCCAGACGATTTTGTTTGCGGGGAAGAGTAGGTATTTTTCTTCATGCCTTT T G RAF1 Ensembl:ENSG00000132155 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:12603482..12606241 32194978 MeRIP-seq:(Medium) rs1254872791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7116565,Human_RBP_ID_23017649 Human_Splice_Rec_395886,Human_Splice_Rec_395887 RMVar_hsa_circ_14332,RMVar_hsa_circ_84407,RMVar_hsa_circ_215987,RMVar_hsa_circ_310115,RMVar_hsa_circ_43270,RMVar_hsa_circ_33183,RMVar_hsa_circ_118584,RMVar_hsa_circ_345790,RMVar_hsa_circ_215990,RMVar_hsa_circ_349801,RMVar_hsa_circ_323691,RMVar_hsa_circ_323838,RMVar_hsa_circ_52302,RMVar_hsa_circ_215991,RMVar_hsa_circ_215992,RMVar_hsa_circ_215993,RMVar_hsa_circ_215994,RMVar_hsa_circ_292156,RMVar_hsa_circ_215996,RMVar_hsa_circ_215995,RMVar_hsa_circ_337943 57536 RMVar_ID_57536 Human_SNP_ID_123138957 m1A Human chr3 + 12663935 12663935 12663935 CGGTCACATTCGGCGCGTCCCCAGCCCAGGGGACGGAGCCCCGAGCAGCCCCCGCATCGTAGCAA CGGTCACATTCGGCGCGTCCCCAGCCCAGGGGCCGGAGCCCCGAGCAGCCCCCGCATCGTAGCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:12663886..12664126 26863196 MeRIP-seq:(Medium) rs1290847333 Functional Loss SNV dbSNP153 33..33 33 - - - 57537 RMVar_ID_57537 Human_SNP_ID_123168047 m1A Human chr3 - 12768967 12768967 12768967 GGACCTGCAGTGCGCCTTGCCTGTGCCTCGCCAGGCCGCGCCCCCCCGCCCCCCCCGCCCCCCCC GGACCTGCAGTGCGCCTTGCCTGTGCCTCGCCTGGCCGCGCCCCCCCGCCCCCCCCGCCCCCCCC T A TMEM40 Ensembl:ENSG00000088726 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:12768916..12769045 26863196 MeRIP-seq:(Medium) rs1475830733 Functional Loss SNV dbSNP153 33..33 33 - - - 57538 RMVar_ID_57538 Human_SNP_ID_123186681 m1A Human chr3 - 12836135 12836135 12836135 TGGAAAGAGCTGCCCAACTGGCCATCAGAGTCACCAACCCCAATGCCAGGCTGCGCAGTGAAGAA TGGAAAGAGCTGCCCAACTGGCCATCAGAGTCCCCAACCCCAATGCCAGGCTGCGCAGTGAAGAA T G RPL32 Ensembl:ENSG00000144713 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12836084..12836194 26863196 MeRIP-seq:(Medium) rs3209282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248321,Human_RBP_ID_588863,Human_RBP_ID_784472,Human_RBP_ID_1102658,Human_RBP_ID_1617517,Human_RBP_ID_1948888,Human_RBP_ID_3685679,Human_RBP_ID_4760752,Human_RBP_ID_8558294,Human_RBP_ID_9131843,Human_RBP_ID_14615209,Human_RBP_ID_18194484,Human_RBP_ID_18796553,Human_RBP_ID_26503371,Human_RBP_ID_26678286,Human_RBP_ID_26823586,Human_RBP_ID_27045083,Human_RBP_ID_27313099 Human_Splice_Rec_396266,Human_Splice_Rec_396272,Human_Splice_Rec_396278,Human_Splice_Rec_396284,Human_Splice_Rec_396288,Human_Splice_Rec_396294 57539 RMVar_ID_57539 Human_SNP_ID_123187830 m1A Human chr3 + 12840227 12840227 12840227 TTTTGACGATCTTGGGCTTCACAAGGGGTCTGAGGGCGGCCATGATGCCTTTTGGGGAAGAAGCG TTTTGACGATCTTGGGCTTCACAAGGGGTCTGGGGGCGGCCATGATGCCTTTTGGGGAAGAAGCG A G CAND2 Ensembl:ENSG00000144712 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:12840176..12840300 26863410 MeRIP-seq:(Medium) rs1366288626 Functional Loss SNV dbSNP153 33..33 33 - - - 57540 RMVar_ID_57540 Human_SNP_ID_123187843 m1A Human chr3 - 12840240 12840240 12840240 CCTCACCTGGGGCCGCTTCTTCCCCAAAAGGCATCATGGCCGCCCTCAGACCCCTTGTGAAGCCC CCTCACCTGGGGCCGCTTCTTCCCCAAAAGGCGTCATGGCCGCCCTCAGACCCCTTGTGAAGCCC T C RPL32 Ensembl:ENSG00000144713 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:12840201..12840250 26863196 MeRIP-seq:(Medium) rs773408400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247386,Human_RBP_ID_783432,Human_RBP_ID_936733,Human_RBP_ID_4756999,Human_RBP_ID_17521363 Human_Splice_Rec_396262,Human_Splice_Rec_396263,Human_Splice_Rec_396269,Human_Splice_Rec_396274,Human_Splice_Rec_396275,Human_Splice_Rec_396281,Human_Splice_Rec_396285,Human_Splice_Rec_396291,Human_Splice_Rec_396296,Human_Splice_Rec_396297,Human_Splice_Rec_396300,Human_Splice_Rec_396301 Human_miRNA_ID_2869365 RMVar_hsa_circ_20188,RMVar_hsa_circ_104498,RMVar_hsa_circ_216022,RMVar_hsa_circ_83962,RMVar_hsa_circ_216023 57541 RMVar_ID_57541 Human_SNP_ID_123187880 m1A Human chr3 + 12840302 12840302 12840302 AGGAAGAATCCTGGAAGGAGGCTTTCCTGCCCAGGGACTGAACACTGTCGCAGAGTGTCTTCCAA AGGAAGAATCCTGGAAGGAGGCTTTCCTGCCCTGGGACTGAACACTGTCGCAGAGTGTCTTCCAA A T CAND2 Ensembl:ENSG00000144712 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:12840298..12840398 32194978 MeRIP-seq:(Medium) rs1485686093 Functional Loss SNV dbSNP153 33..33 33 - - - 57542 RMVar_ID_57542 Human_SNP_ID_123188241 m1A Human chr3 - 12841483 12841483 12841483 GGTGGCAGCCATCTCCTTCTCGGTAAGTGTTAATCCGTGGCAATCCGCATTCCTGCGGGATTCAT GGTGGCAGCCATCTCCTTCTCGGTAAGTGTTAGTCCGTGGCAATCCGCATTCCTGCGGGATTCAT T C RPL32 Ensembl:ENSG00000144713 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:12841476..12841550 26863196 MeRIP-seq:(Medium) rs963474799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1617576,Human_RBP_ID_2747633,Human_RBP_ID_4760762,Human_RBP_ID_5424885,Human_RBP_ID_5473677,Human_RBP_ID_19115065,Human_RBP_ID_22275638,Human_RBP_ID_22822056,Human_RBP_ID_27045116,Human_RBP_ID_27313108,Human_RBP_ID_27497928 RMVar_hsa_circ_104498,RMVar_hsa_circ_216022 57543 RMVar_ID_57543 Human_SNP_ID_123205672 m1A Human chr3 - 12901131 12901131 12901131 ACACCAGTACCACCACGGCCCCCATGGGGGCCACCCAGCCTACGGGGCCCATGCCCACGGCCACC ACACCAGTACCACCACGGCCCCCATGGGGGCCCCCCAGCCTACGGGGCCCATGCCCACGGCCACC T G IQSEC1 Ensembl:ENSG00000144711 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12901082..12901172 26863196 MeRIP-seq:(Medium) rs977222969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212275,Human_RBP_ID_589232,Human_RBP_ID_17292321,Human_RBP_ID_17404872,Human_RBP_ID_17521511 57544 RMVar_ID_57544 Human_SNP_ID_123223643 m1A Human chr3 + 12967078 12967078 12967078 AAGCCCCCAAACTCAAACTCACCCCCACACCAACTTGCACTCCAACAGGCCCTCGATCACACACA AAGCCCCCAAACTCAAACTCACCCCCACACCAGCTTGCACTCCAACAGGCCCTCGATCACACACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:12967072..12967352 26863196 MeRIP-seq:(Medium) rs1216883358 Functional Loss SNV dbSNP153 33..33 33 - - - 57545 RMVar_ID_57545 Human_SNP_ID_123224559 m1A Human chr3 - 12970566 12970566 12970566 ACGAGGCTGGCTGTGCAGGGAGGCTGGGCTTGATCCTGACAGCTTGGAGAGAGGGGCTGCAAAGG ACGAGGCTGGCTGTGCAGGGAGGCTGGGCTTGTTCCTGACAGCTTGGAGAGAGGGGCTGCAAAGG T A IQSEC1 Ensembl:ENSG00000144711 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:12970523..12970607 26863196 MeRIP-seq:(Medium) rs1182346445 Functional Loss SNV dbSNP153 33..33 33 - - - 57546 RMVar_ID_57546 Human_SNP_ID_123312481 m1A Human chr3 - 13317747 13317747 13317747 TTCGCTGCCTCATCACCCACATCTCCCAATGCATTGCCTCCTGCTCGCAAAGCCAGCCCTCCCTC TTCGCTGCCTCATCACCCACATCTCCCAATGCGTTGCCTCCTGCTCGCAAAGCCAGCCCTCCCTC T C NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13317501..13317815 26863196 MeRIP-seq:(Medium) rs1218435172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4723654,Human_RBP_ID_17292327,Human_RBP_ID_17404505,Human_RBP_ID_18169395,Human_RBP_ID_20822886,Human_RBP_ID_22423240 Human_Splice_Rec_396556 57547 RMVar_ID_57547 Human_SNP_ID_123312501 m1A Human chr3 - 13317783 13317783 13317783 TCTGCTGCTAACATCGTCTCTCTTCCCACCCTAGATTTCGCTGCCTCATCACCCACATCTCCCAA TCTGCTGCTAACATCGTCTCTCTTCCCACCCTGGATTTCGCTGCCTCATCACCCACATCTCCCAA T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:13317551..13317800 26863196 MeRIP-seq:(Medium) rs767906021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2749108,Human_RBP_ID_22676020 57548 RMVar_ID_57548 Human_SNP_ID_123314245 m1A Human chr3 - 13323434 13323434 13323434 GCGCTCCATGAAGCTTCCTTGGCTCCCTCTCTAGGTGGTGGTCAGCGTCCCTCAGAGGATCATGG GCGCTCCATGAAGCTTCCTTGGCTCCCTCTCTGGGTGGTGGTCAGCGTCCCTCAGAGGATCATGG T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13323401..13323450 32194978 MeRIP-seq:(Medium) rs369500635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4761230 RMVar_hsa_circ_116747,RMVar_hsa_circ_268389,RMVar_hsa_circ_216033 57549 RMVar_ID_57549 Human_SNP_ID_123317770 m1A Human chr3 - 13336897 13336897 13336897 CTCCCCTGCAGATGCCCATCTATGTCACCGGCATCACCAACCACCAGAACCCTTTCTCCTTTGGC CTCCCCTGCAGATGCCCATCTATGTCACCGGCGTCACCAACCACCAGAACCCTTTCTCCTTTGGC T C NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13336846..13336955 26863196 MeRIP-seq:(Medium) rs1273710939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8559205 Human_Splice_Rec_396530 RMVar_hsa_circ_43835,RMVar_hsa_circ_99145,RMVar_hsa_circ_11311,RMVar_hsa_circ_35171,RMVar_hsa_circ_123641,RMVar_hsa_circ_216034,RMVar_hsa_circ_216035,RMVar_hsa_circ_369818,RMVar_hsa_circ_38977,RMVar_hsa_circ_216036 57550 RMVar_ID_57550 Human_SNP_ID_123318037 m1A Human chr3 + 13337895 13337895 13337895 TGGGGGCGCGGATCCTCACGGCCCTTAGCAGCAGCACCTCCACCTGCACGAGGTCCTGGGGAAAC TGGGGGCGCGGATCCTCACGGCCCTTAGCAGCGGCACCTCCACCTGCACGAGGTCCTGGGGAAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13337826..13337953 26863196 MeRIP-seq:(Medium) rs764496955 Functional Loss SNV dbSNP153 33..33 33 - - - 57551 RMVar_ID_57551 Human_SNP_ID_123318555 m1A Human chr3 + 13339903 13339903 13339903 CCTTGCCGGTCTCTGCATCCACTGCCTGCACGAGCCCAGACACAGTGCCGTTCCCGATGGCGAGG CCTTGCCGGTCTCTGCATCCACTGCCTGCACGGGCCCAGACACAGTGCCGTTCCCGATGGCGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13339808..13339942 26863196 MeRIP-seq:(Medium) rs1210369299 Functional Loss SNV dbSNP153 33..33 33 - - - 57552 RMVar_ID_57552 Human_SNP_ID_123318556 m1A Human chr3 + 13339903 13339903 13339903 CCTTGCCGGTCTCTGCATCCACTGCCTGCACGAGCCCAGACACAGTGCCGTTCCCGATGGCGAGG CCTTGCCGGTCTCTGCATCCACTGCCTGCACGTGCCCAGACACAGTGCCGTTCCCGATGGCGAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13339808..13339942 26863196 MeRIP-seq:(Medium) rs1210369299 Functional Loss SNV dbSNP153 33..33 33 - - - 57553 RMVar_ID_57553 Human_SNP_ID_123319092 m1A Human chr3 - 13341727 13341727 13341727 CAACAGATTGAAGTAAGACGAGTTCTTCCCACACCATGTGGGATCAGCCCAGTGCTGGGGGTTGG CAACAGATTGAAGTAAGACGAGTTCTTCCCACTCCATGTGGGATCAGCCCAGTGCTGGGGGTTGG T A NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:13341726..13341800 26863196 MeRIP-seq:(Medium) rs769011372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115081 RMVar_hsa_circ_99145,RMVar_hsa_circ_35171,RMVar_hsa_circ_123641,RMVar_hsa_circ_216034,RMVar_hsa_circ_216035,RMVar_hsa_circ_112106,RMVar_hsa_circ_78627,RMVar_hsa_circ_38977,RMVar_hsa_circ_113640,RMVar_hsa_circ_216037,RMVar_hsa_circ_216038,RMVar_hsa_circ_52726,RMVar_hsa_circ_122264,RMVar_hsa_circ_265747,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_96062,RMVar_hsa_circ_85725,RMVar_hsa_circ_216043,RMVar_hsa_circ_216040,RMVar_hsa_circ_216041,RMVar_hsa_circ_216039 57554 RMVar_ID_57554 Human_SNP_ID_123319207 m1A Human chr3 + 13342000 13342000 13342000 CCCTCCTCTGACCCCTAGGAGAACTCACACCAATGTAATGATCGGGGAGGCTGCTCGGAGCTTCA CCCTCCTCTGACCCCTAGGAGAACTCACACCAGTGTAATGATCGGGGAGGCTGCTCGGAGCTTCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:13341776..13342075 26863196 MeRIP-seq:(Medium) rs1247450602 Functional Loss SNV dbSNP153 33..33 33 - - - 57555 RMVar_ID_57555 Human_SNP_ID_123319983 m1A Human chr3 - 13344900 13344900 13344900 ACGTGGATGCAGGAAGACTGTTCTGAGGAAGGACGCTGGACCTGGGCCTGGAGGATGACTTGGAG ACGTGGATGCAGGAAGACTGTTCTGAGGAAGGCCGCTGGACCTGGGCCTGGAGGATGACTTGGAG T G NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13344863..13345019 26863196 MeRIP-seq:(Medium) rs1287663541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836855,Human_RBP_ID_7123325,Human_RBP_ID_14629193,Human_RBP_ID_17994482,Human_RBP_ID_23026682,Human_RBP_ID_23119913 RMVar_hsa_circ_99145,RMVar_hsa_circ_216034,RMVar_hsa_circ_112106,RMVar_hsa_circ_78627,RMVar_hsa_circ_216037,RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_96062,RMVar_hsa_circ_216043,RMVar_hsa_circ_216040,RMVar_hsa_circ_216041,RMVar_hsa_circ_97575,RMVar_hsa_circ_126441,RMVar_hsa_circ_216044,RMVar_hsa_circ_216046 57556 RMVar_ID_57556 Human_SNP_ID_123322172 m1A Human chr3 - 13353561 13353561 13353561 CCAGGAGTCCCACCTCAGCTCTGCCAGAACAAAGCAGCCGGTATCTCCCAGGGCCCAGTGGTGGG CCAGGAGTCCCACCTCAGCTCTGCCAGAACAACGCAGCCGGTATCTCCCAGGGCCCAGTGGTGGG T G NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:13353551..13353575 26863196 MeRIP-seq:(Medium) rs1343542388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_396512,Human_Splice_Rec_396513,Human_Splice_Rec_396562,Human_Splice_Rec_396563,Human_Splice_Rec_396596,Human_Splice_Rec_396597 RMVar_hsa_circ_99145,RMVar_hsa_circ_216034,RMVar_hsa_circ_112106,RMVar_hsa_circ_78627,RMVar_hsa_circ_216037,RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_216041,RMVar_hsa_circ_53093,RMVar_hsa_circ_97575,RMVar_hsa_circ_126441,RMVar_hsa_circ_216044,RMVar_hsa_circ_106947,RMVar_hsa_circ_117756,RMVar_hsa_circ_216046,RMVar_hsa_circ_272143,RMVar_hsa_circ_109268,RMVar_hsa_circ_81841,RMVar_hsa_circ_216049,RMVar_hsa_circ_29455,RMVar_hsa_circ_216051,RMVar_hsa_circ_8821,RMVar_hsa_circ_216050,RMVar_hsa_circ_216047,RMVar_hsa_circ_216048,RMVar_hsa_circ_216052,RMVar_hsa_circ_118580 57557 RMVar_ID_57557 Human_SNP_ID_123327013 m1A Human chr3 - 13371989 13371989 13371989 CGAGCCCCACAGCATGGAGTTTGCCCCGTGCCAGGTGGAGGCACGTGTGGGCCAGGCCCTGGAGC CGAGCCCCACAGCATGGAGTTTGCCCCGTGCCGGGTGGAGGCACGTGTGGGCCAGGCCCTGGAGC T C NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13371938..13372072 26863196 MeRIP-seq:(Medium) rs1348056616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_932876,Human_RBP_ID_3963661,Human_RBP_ID_8235987,Human_RBP_ID_18194500,Human_RBP_ID_18471594,Human_RBP_ID_19009878,Human_RBP_ID_22455718,Human_RBP_ID_22769081 Human_Splice_Rec_396502,Human_Splice_Rec_396586 RMVar_hsa_circ_99145,RMVar_hsa_circ_216034,RMVar_hsa_circ_112106,RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_216041,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_117756,RMVar_hsa_circ_216046,RMVar_hsa_circ_109268,RMVar_hsa_circ_81841,RMVar_hsa_circ_216049,RMVar_hsa_circ_29455,RMVar_hsa_circ_216051,RMVar_hsa_circ_8821,RMVar_hsa_circ_216050 57558 RMVar_ID_57558 Human_SNP_ID_123327961 m1A Human chr3 - 13375601 13375601 13375601 GGTCCACATACTACAGGTGCCTGTGTGGAACCAGCAGGAGGTGGAAATTCACATCCCGATCACCC GGTCCACATACTACAGGTGCCTGTGTGGAACCGGCAGGAGGTGGAAATTCACATCCCGATCACCC T C NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13375551..13375650 32194978 MeRIP-seq:(Medium) rs895364937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18013137 Human_Splice_Rec_396499,Human_Splice_Rec_396583 RMVar_hsa_circ_112106,RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_216041,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_117756,RMVar_hsa_circ_216046,RMVar_hsa_circ_109268,RMVar_hsa_circ_29455,RMVar_hsa_circ_216051,RMVar_hsa_circ_8821,RMVar_hsa_circ_216050,RMVar_hsa_circ_367268,RMVar_hsa_circ_377406,RMVar_hsa_circ_38044 57559 RMVar_ID_57559 Human_SNP_ID_123339594 m1A Human chr3 - 13420244 13420244 13420244 GCGGCGCGGGCGGCCGGGCGCAGGGTCGCGGGAGGTGACGCGCGGCGAGGATGGCGGCGCGGGGC GCGGCGCGGGCGGCCGGGCGCAGGGTCGCGGGGGGTGACGCGCGGCGAGGATGGCGGCGCGGGGC T C NUP210 Ensembl:ENSG00000132182 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:13419493..13420325 26863196 MeRIP-seq:(Medium) rs1187281389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836859,Human_RBP_ID_4756317,Human_RBP_ID_8729828,Human_RBP_ID_9333615,Human_RBP_ID_9435291,Human_RBP_ID_22725730 RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 57560 RMVar_ID_57560 Human_SNP_ID_123355331 m1A Human chr3 + 13481215 13481214 13481215 GGGAGGGAGCTGCTTTCTGCCGAGGCTGCCCCAGCTGTGCGTCTGTCTTTTTCCACACGGTAGGC GGGAGGGAGCTGCTTTCTGCCGAGGCTGCCCC_GCTGTGCGTCTGTCTTTTTCCACACGGTAGGC CA C HDAC11 Ensembl:ENSG00000163517 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:13481211..13481341 26863410 MeRIP-seq:(Medium) rs765760173 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22551347 57561 RMVar_ID_57561 Human_SNP_ID_123355332 m1A Human chr3 + 13481215 13481215 13481215 GGGAGGGAGCTGCTTTCTGCCGAGGCTGCCCCAGCTGTGCGTCTGTCTTTTTCCACACGGTAGGC GGGAGGGAGCTGCTTTCTGCCGAGGCTGCCCCTGCTGTGCGTCTGTCTTTTTCCACACGGTAGGC A T HDAC11 Ensembl:ENSG00000163517 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:13481211..13481341 26863410 MeRIP-seq:(Medium) rs757324125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22551347 57562 RMVar_ID_57562 Human_SNP_ID_123357309 m1A Human chr3 - 13487980 13487980 13487980 CTCCCTCACTCCCTTCCCACATGTCACCTGTGATCACAGGTAGTAAGCCCTTTCCTGACTCCTGA CTCCCTCACTCCCTTCCCACATGTCACCTGTGGTCACAGGTAGTAAGCCCTTTCCTGACTCCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:13487968..13488074 26863196 MeRIP-seq:(Medium) rs1395529422 Functional Loss SNV dbSNP153 33..33 33 - - - 57563 RMVar_ID_57563 Human_SNP_ID_123360036 m1A Human chr3 - 13498529 13498529 13498529 ACTCACCCACGTTGATGGCCCAGCCTCGCTCCACAGCCAGCTTCCCCGCCTTTGGAGACAAGCAG ACTCACCCACGTTGATGGCCCAGCCTCGCTCCGCAGCCAGCTTCCCCGCCTTTGGAGACAAGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13498524..13501671 32194978 MeRIP-seq:(Medium) rs552771143 Functional Loss SNV dbSNP153 33..33 33 - - - 57564 RMVar_ID_57564 Human_SNP_ID_123361534 m1A Human chr3 - 13504169 13504169 13504169 CGTCGGGCAGGTGCTCCTGGAGGGATTTCTTGATGTTCCTCTCCACCTTATCCAGGTACTCATCA CGTCGGGCAGGTGCTCCTGGAGGGATTTCTTGGTGTTCCTCTCCACCTTATCCAGGTACTCATCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13504136..13504481 26863196 MeRIP-seq:(Medium) rs1338484405 Functional Loss SNV dbSNP153 33..33 33 - - - 57565 RMVar_ID_57565 Human_SNP_ID_123361762 m1A Human chr3 - 13504681 13504681 13504681 AGGGCCACGTGACAGGCAGGGCAGCAAGGGTCAGGGCACTGCAGGGGGAAGCAGCGGTGTGTCTG AGGGCCACGTGACAGGCAGGGCAGCAAGGGTCGGGGCACTGCAGGGGGAAGCAGCGGTGTGTCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13504580..13504730 26863196 MeRIP-seq:(Medium) rs368703111 Functional Loss SNV dbSNP153 33..33 33 - - - 57566 RMVar_ID_57566 Human_SNP_ID_123362094 m1A Human chr3 + 13506032 13506032 13506032 GGGGGTGCTCCCACTGTCTCCCGGCCTCCCTAATGCTCCCTCTGCTGCAGGGAGAAGGGTTCCAA GGGGGTGCTCCCACTGTCTCCCGGCCTCCCTAGTGCTCCCTCTGCTGCAGGGAGAAGGGTTCCAA A G HDAC11 Ensembl:ENSG00000163517 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13505576..13506125 32194978 MeRIP-seq:(Medium) rs767341820 Functional Loss SNV dbSNP153 33..33 33 - - - 57567 RMVar_ID_57567 Human_SNP_ID_123460212 m1A Human chr3 + 13880037 13880037 13880037 GAGGGAGGGAGGAGCGAGCGCGGCGTGGGGCGACGCCGGGCTGCGCGCGAGCGACCGGTGCAAGT GAGGGAGGGAGGAGCGAGCGCGGCGTGGGGCGGCGCCGGGCTGCGCGCGAGCGACCGGTGCAAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:13879990..13880072 26863196 MeRIP-seq:(Medium) rs553828588 Functional Loss SNV dbSNP153 33..33 33 - - - 57568 RMVar_ID_57568 Human_SNP_ID_123517459 m1A Human chr3 + 14112927 14112927 14112927 ATCCCTCCTCTTCTTTGGTTGCAGTGGCCTCAATGGGAGCTGTTTCTTCTGCTTGTTCTGCTGGC ATCCCTCCTCTTCTTTGGTTGCAGTGGCCTCAGTGGGAGCTGTTTCTTCTGCTTGTTCTGCTGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14112914..14113029 26863196 MeRIP-seq:(Medium) rs751845757 Functional Loss SNV dbSNP153 33..33 33 - - - 57569 RMVar_ID_57569 Human_SNP_ID_123520289 m1A Human chr3 + 14124734 14124734 14124734 GCAGAAGCGGCGGTGGCGGCAGCTGCACCTTTACGCCGTGACCTCCCTCTCCTCTGGCAGGGCGG GCAGAAGCGGCGGTGGCGGCAGCTGCACCTTTCCGCCGTGACCTCCCTCTCCTCTGGCAGGGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:14124623..14124875;chr3:14124685..14124855;chr3:14124672..14124845;chr3:14124628..14124841 26863196 MeRIP-seq:(Medium) rs1400429493 Functional Loss SNV dbSNP153 33..33 33 - - - 57570 RMVar_ID_57570 Human_SNP_ID_123521684 m1A Human chr3 + 14129479 14129479 14129479 AGTTAAAACCAGCTCCCAGCCAGGCTTCCTGGAACGGCTGAGCGAGACCTCGGGTGGGATGTTTG AGTTAAAACCAGCTCCCAGCCAGGCTTCCTGGGACGGCTGAGCGAGACCTCGGGTGGGATGTTTG A G TMEM43 Ensembl:ENSG00000170876 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14129368..14129484 26863196 MeRIP-seq:(Medium) rs760725387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18471596,Human_RBP_ID_22455726,Human_RBP_ID_22768523 Human_Splice_Rec_397078,Human_Splice_Rec_397079,Human_Splice_Rec_397088,Human_Splice_Rec_397089 RMVar_hsa_circ_25304 57571 RMVar_ID_57571 Human_SNP_ID_123521699 m1A Human chr3 - 14129501 14129501 14129501 AGCAGGAAGGCCATGAGCCCCACAAACATCCCACCCGAGGTCTCGCTCAGCCGTTCCAGGAAGCC AGCAGGAAGGCCATGAGCCCCACAAACATCCCTCCCGAGGTCTCGCTCAGCCGTTCCAGGAAGCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:14129451..14129575 26863196 MeRIP-seq:(Medium) rs1474026817 Functional Loss SNV dbSNP153 33..33 33 - - - 57572 RMVar_ID_57572 Human_SNP_ID_123522842 m1A Human chr3 + 14133438 14133438 14133438 GTTGGGATGGAATGCTCTGGGAGGGGCTAGTGAGGGGTGTAAAGTCCATGCAAGATACATCTGAC GTTGGGATGGAATGCTCTGGGAGGGGCTAGTGGGGGGTGTAAAGTCCATGCAAGATACATCTGAC A G TMEM43 Ensembl:ENSG00000170876 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14133434..14133548 26863196 MeRIP-seq:(Medium) rs1349432979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68025,RMVar_hsa_circ_25304,RMVar_hsa_circ_75623,RMVar_hsa_circ_216064 57573 RMVar_ID_57573 Human_SNP_ID_123525243 m1A Human chr3 + 14141751 14141751 14141751 CCCTCCTCATTGCCGGCCTGGCCCTTGTGCCCATCCTTGTTGCTCGGACACGGGTGCCAGCCAAA CCCTCCTCATTGCCGGCCTGGCCCTTGTGCCCGTCCTTGTTGCTCGGACACGGGTGCCAGCCAAA A G TMEM43,AC090004.1 Ensembl:ENSG00000170876,Ensembl:ENSG00000268279 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:14141726..14141750 32194978 MeRIP-seq:(Medium) rs541565919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17292333,Human_RBP_ID_17404883,Human_RBP_ID_22456495,Human_RBP_ID_22768841 Clinvar_Rec_167 57574 RMVar_ID_57574 Human_SNP_ID_123525368 m1A Human chr3 - 14142176 14142176 14142176 AAGCATGGCACTTGTGTGCAGTGATGAGAAGCAGCACACGGCAAGGCTGAGCCCTTTATCAGCAG AAGCATGGCACTTGTGTGCAGTGATGAGAAGCGGCACACGGCAAGGCTGAGCCCTTTATCAGCAG T C lnc-XPC-7 RNACentral:URS0000D5C63D lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:14142126..14142300 32194978 MeRIP-seq:(Medium) rs557868412 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_168 57575 RMVar_ID_57575 Human_SNP_ID_123526471 m1A Human chr3 + 14145749 14145749 14145749 GCTTCACCCTGGGTGAATCTGACAAGGGCTGGAGCCAGACGGGACCTGCAGCACCTCCTCAGCTT GCTTCACCCTGGGTGAATCTGACAAGGGCTGGGGCCAGACGGGACCTGCAGCACCTCCTCAGCTT A G AC090004.1,AC093495.1 Ensembl:ENSG00000268279,Ensembl:ENSG00000228242 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14145701..14145875 26863196 MeRIP-seq:(Medium) rs3731178 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_5603539 Clinvar_Rec_169 57576 RMVar_ID_57576 Human_SNP_ID_123526482 m1A Human chr3 + 14145769 14145768 14145769 GACAAGGGCTGGAGCCAGACGGGACCTGCAGCACCTCCTCAGCTTGGCCTCGTCTCCCCTGACCC GACAAGGGCTGGAGCCAGACGGGACCTGCAGC_CCTCCTCAGCTTGGCCTCGTCTCCCCTGACCC CA C AC090004.1,AC093495.1 Ensembl:ENSG00000268279,Ensembl:ENSG00000228242 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14145720..14145843 26863196 MeRIP-seq:(Medium) rs1276043691 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5603539 57577 RMVar_ID_57577 Human_SNP_ID_123528214 m1A Human chr3 + 14151484 14151484 14151484 GCAGAGAAAATCCTCAGCAACCCTGCAGGCCCAGGCAGGGGGCATCGCCCACTCCAGCCTGCTGC GCAGAGAAAATCCTCAGCAACCCTGCAGGCCCGGGCAGGGGGCATCGCCCACTCCAGCCTGCTGC A G AC093495.1 Ensembl:ENSG00000228242 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:14151479..14151591 26863196 MeRIP-seq:(Medium) rs1040857769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8560786 57578 RMVar_ID_57578 Human_SNP_ID_123528215 m1A Human chr3 + 14151484 14151484 14151484 GCAGAGAAAATCCTCAGCAACCCTGCAGGCCCAGGCAGGGGGCATCGCCCACTCCAGCCTGCTGC GCAGAGAAAATCCTCAGCAACCCTGCAGGCCCTGGCAGGGGGCATCGCCCACTCCAGCCTGCTGC A T AC093495.1 Ensembl:ENSG00000228242 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:14151479..14151591 26863196 MeRIP-seq:(Medium) rs1040857769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8560786 57579 RMVar_ID_57579 Human_SNP_ID_123529434 m1A Human chr3 - 14156383 14156383 14156383 GCATCTCCTGAAATATGAGGCCATCTATCCCGAGACAGCTGCCATCCTTGGGTATTGTCGTGGAG GCATCTCCTGAAATATGAGGCCATCTATCCCGGGACAGCTGCCATCCTTGGGTATTGTCGTGGAG T C XPC Ensembl:ENSG00000154767 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14156304..14156386 26863196 MeRIP-seq:(Medium) rs777771958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8874834,Human_RBP_ID_18798581 Human_Splice_Rec_397227,Human_Splice_Rec_397255 RMVar_hsa_circ_216066,RMVar_hsa_circ_60924,RMVar_hsa_circ_371615,RMVar_hsa_circ_316132,RMVar_hsa_circ_364754,RMVar_hsa_circ_216067 57580 RMVar_ID_57580 Human_SNP_ID_123529972 m1A Human chr3 + 14158240 14158238 14158240 AACAGGTCAGAGGCTGGCCCACCACACCGTGCACACAGTCTACACATACCCACTTTTCCTCCTGC AACAGGTCAGAGGCTGGCCCACCACACCGTG__CACAGTCTACACATACCCACTTTTCCTCCTGC GCA G AC093495.1 Ensembl:ENSG00000228242 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14158189..14158396 26863196 MeRIP-seq:(Medium) rs754532049 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_170 57581 RMVar_ID_57581 Human_SNP_ID_123530163 m1A Human chr3 - 14158654 14158654 14158654 CGAGGAAGATGAGGGCCCAGGAGACAAGCAGGAGAAGGCAACCCAGCGACGTCCGCATGGCCGGG CGAGGAAGATGAGGGCCCAGGAGACAAGCAGGGGAAGGCAACCCAGCGACGTCCGCATGGCCGGG T C XPC Ensembl:ENSG00000154767 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14158604..14158741 26863196 MeRIP-seq:(Medium) rs587778762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8875389,Human_RBP_ID_9393330,Human_RBP_ID_18413230,Human_RBP_ID_26346499,Human_RBP_ID_27821932 Human_miRNA_ID_1359556 Clinvar_Rec_171 RMVar_hsa_circ_2932,RMVar_hsa_circ_216066,RMVar_hsa_circ_60924,RMVar_hsa_circ_371615,RMVar_hsa_circ_51469,RMVar_hsa_circ_316132,RMVar_hsa_circ_364754,RMVar_hsa_circ_216067,RMVar_hsa_circ_29167 57582 RMVar_ID_57582 Human_SNP_ID_123533737 m1A Human chr3 + 14173061 14173061 14173061 CTCTTCTTTGGGGGTTTCTCATCTTCAAAGGCATCTAGGTGACAACACAGAACATAAGGTGAGGG CTCTTCTTTGGGGGTTTCTCATCTTCAAAGGCTTCTAGGTGACAACACAGAACATAAGGTGAGGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:14172976..14173118;chr3:14172831..14173111;chr3:14172951..14173126;chr3:14173043..14173127 26863196 MeRIP-seq:(Medium) rs202128104 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57583 RMVar_ID_57583 Human_SNP_ID_123535469 m1A Human chr3 + 14178880 14178880 14178880 CAGGGTTTGAAACATGGCGGACGACGTAGACCAGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG CAGGGTTTGAAACATGGCGGACGACGTAGACCCGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG A C LSM3 Ensembl:ENSG00000170860 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:14178826..14178900 26863410 MeRIP-seq:(Medium) rs200658802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393339 Human_Splice_Rec_397301 57584 RMVar_ID_57584 Human_SNP_ID_123535470 m1A Human chr3 + 14178880 14178880 14178880 CAGGGTTTGAAACATGGCGGACGACGTAGACCAGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG CAGGGTTTGAAACATGGCGGACGACGTAGACCTGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG A T LSM3 Ensembl:ENSG00000170860 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:14178826..14178900 26863410 MeRIP-seq:(Medium) rs200658802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393339 Human_Splice_Rec_397301 57585 RMVar_ID_57585 Human_SNP_ID_123536265 m1A Human chr3 + 14181565 14181565 14181565 CATTACTAATCCTGTTTCTTTTATCAGCAACAAACTACCAACACTGTAGAGGAGCCCCTGGATCT CATTACTAATCCTGTTTCTTTTATCAGCAACAGACTACCAACACTGTAGAGGAGCCCCTGGATCT A G LSM3 Ensembl:ENSG00000170860 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:14181551..14181675;chr3:14178783..14184000;chr3:14178803..14181675 26863410,26863196,26863196 MeRIP-seq:(Medium) rs761249917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_591329,Human_RBP_ID_9393340,Human_RBP_ID_14654907,Human_RBP_ID_26347773,Human_RBP_ID_27046742 Human_Splice_Rec_397302 57586 RMVar_ID_57586 Human_SNP_ID_123601923 m1A Human chr3 - 14440432 14440432 14440432 CCCCATCTTCCCTCTCCCCTTCTCCTTGGGACACGGGCCACACAGAACTGCTTTAGTCCCTCCTA CCCCATCTTCCCTCTCCCCTTCTCCTTGGGACTCGGGCCACACAGAACTGCTTTAGTCCCTCCTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14440427..14440520 26863196 MeRIP-seq:(Medium) rs1485933862 Functional Loss SNV dbSNP153 33..33 33 - - - 57587 RMVar_ID_57587 Human_SNP_ID_123610360 m1A Human chr3 + 14473628 14473628 14473628 CAAGGTCAAGAGCAGAGCAGGGGATTTGGCAGAGAAGGGGGCAGGATTAGCAGAGAAGACAGAAC CAAGGTCAAGAGCAGAGCAGGGGATTTGGCAGGGAAGGGGGCAGGATTAGCAGAGAAGACAGAAC A G SLC6A6 Ensembl:ENSG00000131389 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:14473577..14473682 26863196 MeRIP-seq:(Medium) rs983476089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50615,RMVar_hsa_circ_76105,RMVar_hsa_circ_119640,RMVar_hsa_circ_216076,RMVar_hsa_circ_216079,RMVar_hsa_circ_375112,RMVar_hsa_circ_216080,RMVar_hsa_circ_109670,RMVar_hsa_circ_216081 57588 RMVar_ID_57588 Human_SNP_ID_123624252 m1A Human chr3 + 14525945 14525945 14525945 TTGGAGTAGGGCCCATCGTCTGCAGGAGAGAAAGAGGGAAAGGCCGAGTTCCACTTTCGTTTCCA TTGGAGTAGGGCCCATCGTCTGCAGGAGAGAAGGAGGGAAAGGCCGAGTTCCACTTTCGTTTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14525861..14526051 26863196 MeRIP-seq:(Medium) rs1359797251 Functional Loss SNV dbSNP153 33..33 33 - - - 57589 RMVar_ID_57589 Human_SNP_ID_123659270 m1A Human chr3 + 14668100 14668100 14668100 AACGAGAAAACATAAAGGAAAAGCGAAAGGCTATCTTAGAGGCAAGACTTGCCAAACTTCGACAA AACGAGAAAACATAAAGGAAAAGCGAAAGGCTGTCTTAGAGGCAAGACTTGCCAAACTTCGACAA A G CCDC174 Ensembl:ENSG00000154781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:14668007..14668136 26863196 MeRIP-seq:(Medium) rs542404527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5390548 Human_Splice_Rec_397690,Human_Splice_Rec_397691,Human_Splice_Rec_397731 57590 RMVar_ID_57590 Human_SNP_ID_123660042 m1A Human chr3 + 14671070 14671070 14671070 AGCACAGAGTGACCCAGGGCAGTGCCCTGACCAGAGCCACGGACCTAGCCCTGAACATACGTCAC AGCACAGAGTGACCCAGGGCAGTGCCCTGACCGGAGCCACGGACCTAGCCCTGAACATACGTCAC A G CCDC174 Ensembl:ENSG00000154781 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14671019..14671129 26863196 MeRIP-seq:(Medium) rs1168559687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248354 57591 RMVar_ID_57591 Human_SNP_ID_123728672 m1A Human chr3 + 14943531 14943526 14943531 CCTACGGGGGCTCGCAGTGTGGGCAGGTGCTGAGCTAACGCACACACACAAGGGCTGGGTACTGC CCTACGGGGGCTCGCAGTGTGGGCAGGT_____GCTAACGCACACACACAAGGGCTGGGTACTGC TGCTGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:14943480..14943588 26863196 MeRIP-seq:(Medium) rs1012719247 Functional Loss DEL dbSNP153 29..33 33 - - - 57592 RMVar_ID_57592 Human_SNP_ID_123728673 m1A Human chr3 - 14943526 14943526 14943526 ACCCAGCCCTTGTGTGTGTGCGTTAGCTCAGCACCTGCCCACACTGCGAGCCCCCGTAGGATGTG ACCCAGCCCTTGTGTGTGTGCGTTAGCTCAGCGCCTGCCCACACTGCGAGCCCCCGTAGGATGTG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:14943476..14943550 26863196 MeRIP-seq:(Medium) rs1192947055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592323,Human_RBP_ID_936363,Human_RBP_ID_1104420,Human_RBP_ID_5102095,Human_RBP_ID_5654848,Human_RBP_ID_7135743,Human_RBP_ID_8211167,Human_RBP_ID_17292613,Human_RBP_ID_23976776 57593 RMVar_ID_57593 Human_SNP_ID_123729147 m1A Human chr3 - 14944928 14944928 14944928 TGGCTCATGCCTGTAATCCCAGCATTTTGGGAAGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG TGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1142981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592374,Human_RBP_ID_5654819,Human_RBP_ID_26510847 RMVar_hsa_circ_216093,RMVar_hsa_circ_112835 57594 RMVar_ID_57594 Human_SNP_ID_123730045 m1A Human chr3 - 14947392 14947392 14947392 CGCCGGCCTTGGCCGCGGCCGGGCGGGCGGATATGTGGCTTAAATGGCGCAGGCGTCGGGGCCTA CGCCGGCCTTGGCCGCGGCCGGGCGGGCGGATCTGTGGCTTAAATGGCGCAGGCGTCGGGGCCTA T G FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:14947341..14947424 26863196 MeRIP-seq:(Medium) rs892697913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834768,Human_RBP_ID_4726962,Human_RBP_ID_5089767,Human_RBP_ID_5207563,Human_RBP_ID_5605656,Human_RBP_ID_5654824,Human_RBP_ID_18499609,Human_RBP_ID_27047238 RMVar_hsa_circ_216093,RMVar_hsa_circ_112835 57595 RMVar_ID_57595 Human_SNP_ID_123730255 m1A Human chr3 - 14947718 14947718 14947718 CGAGACGCCGAGGTGGGAGCGGGGTGGCGGGGACGGGCCCGGGGGCGCCGCCGGGGTCGCGGAGA CGAGACGCCGAGGTGGGAGCGGGGTGGCGGGGCCGGGCCCGGGGGCGCCGCCGGGGTCGCGGAGA T G FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:14947626..14947931 26863196 MeRIP-seq:(Medium) rs1384983114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3720718,Human_RBP_ID_5325454,Human_RBP_ID_8211271,Human_RBP_ID_8265287,Human_RBP_ID_9333619,Human_RBP_ID_9435061,Human_RBP_ID_18464583 57596 RMVar_ID_57596 Human_SNP_ID_123730280 m1A Human chr3 - 14947755 14947755 14947755 CCGGGGGCCGCGGGCTCGCGGGGCAGCGGGCGAGAGACGAGACGCCGAGGTGGGAGCGGGGTGGC CCGGGGGCCGCGGGCTCGCGGGGCAGCGGGCGGGAGACGAGACGCCGAGGTGGGAGCGGGGTGGC T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr3:14947326..14948658;chr3:14947708..14947837 26863196 MeRIP-seq:(Medium) rs1169901613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11375,Human_RBP_ID_5605658 Human_Splice_Rec_398017,Human_Splice_Rec_398019 57597 RMVar_ID_57597 Human_SNP_ID_123730281 m1A Human chr3 - 14947755 14947755 14947755 CCGGGGGCCGCGGGCTCGCGGGGCAGCGGGCGAGAGACGAGACGCCGAGGTGGGAGCGGGGTGGC CCGGGGGCCGCGGGCTCGCGGGGCAGCGGGCGCGAGACGAGACGCCGAGGTGGGAGCGGGGTGGC T G FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr3:14947326..14948658;chr3:14947708..14947837 26863196 MeRIP-seq:(Medium) rs1169901613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11375,Human_RBP_ID_5605658 Human_Splice_Rec_398017,Human_Splice_Rec_398019 57598 RMVar_ID_57598 Human_SNP_ID_123730286 m1A Human chr3 - 14947763 14947763 14947763 GCGGGAGCCCGGGGGCCGCGGGCTCGCGGGGCAGCGGGCGAGAGACGAGACGCCGAGGTGGGAGC GCGGGAGCCCGGGGGCCGCGGGCTCGCGGGGCCGCGGGCGAGAGACGAGACGCCGAGGTGGGAGC T G FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr3:14947662..14947875;chr3:14947576..14948658 26863196,26863410 MeRIP-seq:(Medium) rs1184382152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11375,Human_RBP_ID_5089768,Human_RBP_ID_5605658,Human_RBP_ID_26763233 Human_Splice_Rec_398017,Human_Splice_Rec_398019 57599 RMVar_ID_57599 Human_SNP_ID_452837024 m1A Human chr11 + 207220 207220 207220 CCTCTCGGCCGAGGTCACCCCAGCTGGGCCAGAGGCAGGCGCACGCGGCTCTACAGGCAGCGGCG CCTCTCGGCCGAGGTCACCCCAGCTGGGCCAGTGGCAGGCGCACGCGGCTCTACAGGCAGCGGCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:207214..207339 26863196 MeRIP-seq:(Medium) rs1264373250 Functional Loss SNV dbSNP153 33..33 33 - - - 57600 RMVar_ID_57600 Human_SNP_ID_452837440 m1A Human chr11 - 208239 208239 208239 CAACGGGCTGTGAGGAAGTGCTGTTTTTGCTGACACCGGACGGTGGGAAGTGAGCCGGGAAAAGA CAACGGGCTGTGAGGAAGTGCTGTTTTTGCTGCCACCGGACGGTGGGAAGTGAGCCGGGAAAAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:208188..208307 26863196 MeRIP-seq:(Medium) rs1400162168 Functional Loss SNV dbSNP153 33..33 33 - - - 57601 RMVar_ID_57601 Human_SNP_ID_452837645 m1A Human chr11 - 208841 208841 208841 CAACCGCCCGGGGCTCCATGGCGCGCCGGGGAAGGCGGGACGGGCCCTTCCTCAGCCGTTCCGGG CAACCGCCCGGGGCTCCATGGCGCGCCGGGGAGGGCGGGACGGGCCCTTCCTCAGCCGTTCCGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr11:208751..208950;chr11:208776..209187 26863410,26863196 MeRIP-seq:(Medium) rs778055462 Functional Loss SNV dbSNP153 33..33 33 - - - 57602 RMVar_ID_57602 Human_SNP_ID_452837667 m1A Human chr11 - 208872 208872 208872 ACATCCTCCTCACCCGTCTCCACGGCTTCTGCAACCGCCCGGGGCTCCATGGCGCGCCGGGGAAG ACATCCTCCTCACCCGTCTCCACGGCTTCTGCCACCGCCCGGGGCTCCATGGCGCGCCGGGGAAG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:208826..209018 26863196 MeRIP-seq:(Medium) rs749034397 Functional Loss SNV dbSNP153 33..33 33 - - - 57603 RMVar_ID_57603 Human_SNP_ID_452837685 m1A Human chr11 + 208901 208901 208901 GGTTGCAGAAGCCGTGGAGACGGGTGAGGAGGATGTGATTATGGAAGCTCTGCGGTCATACAACC GGTTGCAGAAGCCGTGGAGACGGGTGAGGAGGGTGTGATTATGGAAGCTCTGCGGTCATACAACC A G RIC8A Ensembl:ENSG00000177963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:208801..209094 26863196 MeRIP-seq:(Medium) rs1261876099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184518,Human_RBP_ID_8348571,Human_RBP_ID_17793658,Human_RBP_ID_23499098,Human_RBP_ID_26319414 Human_Splice_Rec_1192001,Human_Splice_Rec_1192019,Human_Splice_Rec_1192037,Human_Splice_Rec_1192041,Human_Splice_Rec_1192047,Human_Splice_Rec_1192049,Human_Splice_Rec_1192053 RMVar_hsa_circ_127940,RMVar_hsa_circ_147348 57604 RMVar_ID_57604 Human_SNP_ID_452839231 m1A Human chr11 + 213399 213399 213399 AGAAGGAGCACGAGGCCATGAAGCTGGTGACCATGTTTGACAAGCTCTCCAGGTGTGTGGCATGA AGAAGGAGCACGAGGCCATGAAGCTGGTGACCGTGTTTGACAAGCTCTCCAGGTGTGTGGCATGA A G RIC8A Ensembl:ENSG00000177963 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:213349..213456 26863196 MeRIP-seq:(Medium) rs369229712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809054,Human_RBP_ID_19050674 Human_Splice_Rec_1192017,Human_Splice_Rec_1192035,Human_Splice_Rec_1192067,Human_Splice_Rec_1192093,Human_Splice_Rec_1192097,Human_Splice_Rec_1192099,Human_Splice_Rec_1192101 RMVar_hsa_circ_88652,RMVar_hsa_circ_147351 57605 RMVar_ID_57605 Human_SNP_ID_452839547 m1A Human chr11 - 214406 214406 214406 GTGGGATGTGGCTTCCCCAGGTTGCAACCCCAAGGAAGTCTCTGGAAGCAGCACCAGTCCTGATG GTGGGATGTGGCTTCCCCAGGTTGCAACCCCAGGGAAGTCTCTGGAAGCAGCACCAGTCCTGATG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:214314..214465 32194978 MeRIP-seq:(Medium) rs1473495694 Functional Loss SNV dbSNP153 33..33 33 - - - 57606 RMVar_ID_57606 Human_SNP_ID_452840158 m1A Human chr11 + 216612 216612 216612 CTCAGTTCACATATTCTGGTTTCACCTGCCCAAGCTGTCTTCAGGCATGAGGTCTTGTCAGAATT CTCAGTTCACATATTCTGGTTTCACCTGCCCAGGCTGTCTTCAGGCATGAGGTCTTGTCAGAATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:216200..216647 32194978 MeRIP-seq:(Medium) rs1437071334 Functional Loss SNV dbSNP153 33..33 33 - - - 57607 RMVar_ID_57607 Human_SNP_ID_452841909 m1A Human chr11 - 223250 223250 223250 CGGTTCTGTGTGTGTCTGAGGTGTCGGGAAACATGCCCTGGATGTGTTCAAGCAGCTGTTCTGCG CGGTTCTGTGTGTGTCTGAGGTGTCGGGAAACGTGCCCTGGATGTGTTCAAGCAGCTGTTCTGCG T C SIRT3 Ensembl:ENSG00000142082 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:223246..223584 26863196 MeRIP-seq:(Medium) rs1245628458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385825,Human_RBP_ID_17110210 RMVar_hsa_circ_42587 57608 RMVar_ID_57608 Human_SNP_ID_452842017 m1A Human chr11 + 223670 223670 223670 CTCACACGTGGTGCCCCACCCACACCTATACCACCTCCAAAGCCCAGCAGCTTCCCACCTTCCTG CTCACACGTGGTGCCCCACCCACACCTATACCCCCTCCAAAGCCCAGCAGCTTCCCACCTTCCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:223661..223777 26863196 MeRIP-seq:(Medium) rs1216167551 Functional Loss SNV dbSNP153 33..33 33 - - - 57609 RMVar_ID_57609 Human_SNP_ID_452845120 m1A Human chr11 - 234102 234102 234102 TTTCAGTGACTCACAAACATTTTATTTACGTAAATGAGGAATGTACTCAGGCACCCTTCGTGATA TTTCAGTGACTCACAAACATTTTATTTACGTATATGAGGAATGTACTCAGGCACCCTTCGTGATA T A SIRT3 Ensembl:ENSG00000142082 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10794302 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6732,GWAS_ID_6733,GWAS_ID_6734,GWAS_ID_6735,GWAS_ID_6736,GWAS_ID_6737,GWAS_ID_6738,GWAS_ID_6739,GWAS_ID_6740,GWAS_ID_6741,GWAS_ID_6742,GWAS_ID_6743,GWAS_ID_6744,GWAS_ID_6745,GWAS_ID_6746,GWAS_ID_6747,GWAS_ID_6748,GWAS_ID_6749,GWAS_ID_6750,GWAS_ID_6751,GWAS_ID_6752,GWAS_ID_6753,GWAS_ID_6754,GWAS_ID_6755,GWAS_ID_6756,GWAS_ID_6757,GWAS_ID_6758,GWAS_ID_6759,GWAS_ID_6760,GWAS_ID_6761,GWAS_ID_6762,GWAS_ID_6763,GWAS_ID_6764,GWAS_ID_6765,GWAS_ID_6766,GWAS_ID_6767,GWAS_ID_6768,GWAS_ID_6769,GWAS_ID_6770,GWAS_ID_6771,GWAS_ID_6772,GWAS_ID_6773,GWAS_ID_6774,GWAS_ID_6775,GWAS_ID_6776,GWAS_ID_6777,GWAS_ID_6778,GWAS_ID_6779,GWAS_ID_6780,GWAS_ID_6781,GWAS_ID_6782,GWAS_ID_6783,GWAS_ID_6784,GWAS_ID_6785,GWAS_ID_6786,GWAS_ID_6787,GWAS_ID_6788,GWAS_ID_6789,GWAS_ID_6790,GWAS_ID_6791,GWAS_ID_6792,GWAS_ID_6793,GWAS_ID_6794,GWAS_ID_6795,GWAS_ID_6796 RMVar_hsa_circ_147357,RMVar_hsa_circ_75729 57610 RMVar_ID_57610 Human_SNP_ID_452845121 m1A Human chr11 - 234102 234102 234102 TTTCAGTGACTCACAAACATTTTATTTACGTAAATGAGGAATGTACTCAGGCACCCTTCGTGATA TTTCAGTGACTCACAAACATTTTATTTACGTAGATGAGGAATGTACTCAGGCACCCTTCGTGATA T C SIRT3 Ensembl:ENSG00000142082 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10794302 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6732,GWAS_ID_6733,GWAS_ID_6734,GWAS_ID_6735,GWAS_ID_6736,GWAS_ID_6737,GWAS_ID_6738,GWAS_ID_6739,GWAS_ID_6740,GWAS_ID_6741,GWAS_ID_6742,GWAS_ID_6743,GWAS_ID_6744,GWAS_ID_6745,GWAS_ID_6746,GWAS_ID_6747,GWAS_ID_6748,GWAS_ID_6749,GWAS_ID_6750,GWAS_ID_6751,GWAS_ID_6752,GWAS_ID_6753,GWAS_ID_6754,GWAS_ID_6755,GWAS_ID_6756,GWAS_ID_6757,GWAS_ID_6758,GWAS_ID_6759,GWAS_ID_6760,GWAS_ID_6761,GWAS_ID_6762,GWAS_ID_6763,GWAS_ID_6764,GWAS_ID_6765,GWAS_ID_6766,GWAS_ID_6767,GWAS_ID_6768,GWAS_ID_6769,GWAS_ID_6770,GWAS_ID_6771,GWAS_ID_6772,GWAS_ID_6773,GWAS_ID_6774,GWAS_ID_6775,GWAS_ID_6776,GWAS_ID_6777,GWAS_ID_6778,GWAS_ID_6779,GWAS_ID_6780,GWAS_ID_6781,GWAS_ID_6782,GWAS_ID_6783,GWAS_ID_6784,GWAS_ID_6785,GWAS_ID_6786,GWAS_ID_6787,GWAS_ID_6788,GWAS_ID_6789,GWAS_ID_6790,GWAS_ID_6791,GWAS_ID_6792,GWAS_ID_6793,GWAS_ID_6794,GWAS_ID_6795,GWAS_ID_6796 RMVar_hsa_circ_147357,RMVar_hsa_circ_75729 57611 RMVar_ID_57611 Human_SNP_ID_452845858 m1A Human chr11 + 236213 236213 236213 GCCCCGCACTCACATCGTCCCTGCCGCCAAGCACCAGCCGACAGCCGCAGGCCTGAAACGGCCCC GCCCCGCACTCACATCGTCCCTGCCGCCAAGCCCCAGCCGACAGCCGCAGGCCTGAAACGGCCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:236167..236331 26863196 MeRIP-seq:(Medium) rs963825344 Functional Loss SNV dbSNP153 33..33 33 - - - 57612 RMVar_ID_57612 Human_SNP_ID_452846436 m1A Human chr11 - 237168 237168 237168 GCCCCCTCCGTCTCCCTCTATCGCCGGGGCCCAGGGCCCGTCTGCTCGGCGCTCACTTCTTCGTG GCCCCCTCCGTCTCCCTCTATCGCCGGGGCCCGGGGCCCGTCTGCTCGGCGCTCACTTCTTCGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:237163..237300 26863196 MeRIP-seq:(Medium) rs763093879 Functional Loss SNV dbSNP153 33..33 33 - - - 57613 RMVar_ID_57613 Human_SNP_ID_452846446 m1A Human chr11 + 237180 237180 237180 AGCGCCGAGCAGACGGGCCCTGGGCCCCGGCGATAGAGGGAGACGGAGGGGGCAGGCGGGCGGAG AGCGCCGAGCAGACGGGCCCTGGGCCCCGGCGGTAGAGGGAGACGGAGGGGGCAGGCGGGCGGAG A G PSMD13 Ensembl:ENSG00000185627 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:237171..237328 26863196 MeRIP-seq:(Medium) rs376058802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228084,Human_RBP_ID_19050678 57614 RMVar_ID_57614 Human_SNP_ID_452846447 m1A Human chr11 + 237180 237180 237180 AGCGCCGAGCAGACGGGCCCTGGGCCCCGGCGATAGAGGGAGACGGAGGGGGCAGGCGGGCGGAG AGCGCCGAGCAGACGGGCCCTGGGCCCCGGCGTTAGAGGGAGACGGAGGGGGCAGGCGGGCGGAG A T PSMD13 Ensembl:ENSG00000185627 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:237171..237328 26863196 MeRIP-seq:(Medium) rs376058802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228084,Human_RBP_ID_19050678 57615 RMVar_ID_57615 Human_SNP_ID_452850856 m1A Human chr11 + 251918 251918 251918 AAACGAGTCCACATGACCTGGGTGCAGCCCCGAGTGTTGGATTTGCAACAGGTGATGTGTTTGAA AAACGAGTCCACATGACCTGGGTGCAGCCCCGGGTGTTGGATTTGCAACAGGTGATGTGTTTGAA A G PSMD13 Ensembl:ENSG00000185627 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:251801..251950 32194978 MeRIP-seq:(Medium) rs775295951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393944,Human_RBP_ID_5110308,Human_RBP_ID_8348861,Human_RBP_ID_18606215,Human_RBP_ID_18971483,Human_RBP_ID_22432676,Human_RBP_ID_23499429 Human_Splice_Rec_1192262,Human_Splice_Rec_1192263,Human_Splice_Rec_1192290,Human_Splice_Rec_1192291,Human_Splice_Rec_1192330,Human_Splice_Rec_1192350,Human_Splice_Rec_1192351,Human_Splice_Rec_1192382,Human_Splice_Rec_1192383,Human_Splice_Rec_1192404,Human_Splice_Rec_1192405,Human_Splice_Rec_1192424,Human_Splice_Rec_1192428,Human_Splice_Rec_1192429,Human_Splice_Rec_1192431 RMVar_hsa_circ_32282,RMVar_hsa_circ_124468,RMVar_hsa_circ_147361,RMVar_hsa_circ_80540,RMVar_hsa_circ_125066,RMVar_hsa_circ_147367,RMVar_hsa_circ_147368 57616 RMVar_ID_57616 Human_SNP_ID_452850857 m1A Human chr11 + 251918 251918 251918 AAACGAGTCCACATGACCTGGGTGCAGCCCCGAGTGTTGGATTTGCAACAGGTGATGTGTTTGAA AAACGAGTCCACATGACCTGGGTGCAGCCCCGTGTGTTGGATTTGCAACAGGTGATGTGTTTGAA A T PSMD13 Ensembl:ENSG00000185627 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:251801..251950 32194978 MeRIP-seq:(Medium) rs775295951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393944,Human_RBP_ID_5110308,Human_RBP_ID_8348861,Human_RBP_ID_18606215,Human_RBP_ID_18971483,Human_RBP_ID_22432676,Human_RBP_ID_23499429 Human_Splice_Rec_1192262,Human_Splice_Rec_1192263,Human_Splice_Rec_1192290,Human_Splice_Rec_1192291,Human_Splice_Rec_1192330,Human_Splice_Rec_1192350,Human_Splice_Rec_1192351,Human_Splice_Rec_1192382,Human_Splice_Rec_1192383,Human_Splice_Rec_1192404,Human_Splice_Rec_1192405,Human_Splice_Rec_1192424,Human_Splice_Rec_1192428,Human_Splice_Rec_1192429,Human_Splice_Rec_1192431 RMVar_hsa_circ_32282,RMVar_hsa_circ_124468,RMVar_hsa_circ_147361,RMVar_hsa_circ_80540,RMVar_hsa_circ_125066,RMVar_hsa_circ_147367,RMVar_hsa_circ_147368 57617 RMVar_ID_57617 Human_SNP_ID_452851011 m1A Human chr11 - 252487 252487 252487 CTTCATTCCCTTGATCTGAAATGGAAATCCGGACACAAGGGACGTTAAGACACGCAGGAGACACA CTTCATTCCCTTGATCTGAAATGGAAATCCGGCCACAAGGGACGTTAAGACACGCAGGAGACACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:252483..252595 26863196 MeRIP-seq:(Medium) rs763454969 Functional Loss SNV dbSNP153 33..33 33 - - - 57618 RMVar_ID_57618 Human_SNP_ID_452851109 m1A Human chr11 + 252784 252784 252784 CTGTCCCTGATGGGAGCCAGGCCACAGGGAGGAGGCTTCTTTGTGGGTCTCTCCTGCAGAGGGTG CTGTCCCTGATGGGAGCCAGGCCACAGGGAGGCGGCTTCTTTGTGGGTCTCTCCTGCAGAGGGTG A C PSMD13 Ensembl:ENSG00000185627 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:252735..252843 26863196 MeRIP-seq:(Medium) rs7116231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393952,Human_RBP_ID_986641,Human_RBP_ID_5110672,Human_RBP_ID_5138445,Human_RBP_ID_17649356,Human_RBP_ID_18159089,Human_RBP_ID_23207159 Human_miRNA_ID_1260985,Human_miRNA_ID_1338642,Human_miRNA_ID_1954608,Human_miRNA_ID_1954609,Human_miRNA_ID_2136699,Human_miRNA_ID_2136700,Human_miRNA_ID_2665492,Human_miRNA_ID_2665493,Human_miRNA_ID_3061578,Human_miRNA_ID_3061579 RMVar_hsa_circ_124468,RMVar_hsa_circ_147361,RMVar_hsa_circ_80540,RMVar_hsa_circ_125066,RMVar_hsa_circ_147367,RMVar_hsa_circ_147368 57619 RMVar_ID_57619 Human_SNP_ID_452851122 m1A Human chr11 + 252825 252825 252825 TGTGGGTCTCTCCTGCAGAGGGTGGGGGTCTCAGGGTCTTAGGTGATACGGGAGAGAAAGAACGT TGTGGGTCTCTCCTGCAGAGGGTGGGGGTCTCGGGGTCTTAGGTGATACGGGAGAGAAAGAACGT A G PSMD13 Ensembl:ENSG00000185627 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:252776..252850 32194978 MeRIP-seq:(Medium) rs1343887482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393952,Human_RBP_ID_5110310,Human_RBP_ID_5138445,Human_RBP_ID_6062684,Human_RBP_ID_9352668,Human_RBP_ID_17649356,Human_RBP_ID_17793807,Human_RBP_ID_18159089,Human_RBP_ID_18432587,Human_RBP_ID_23206779,Human_RBP_ID_26408152 Human_miRNA_ID_75392,Human_miRNA_ID_78561,Human_miRNA_ID_119158,Human_miRNA_ID_122965,Human_miRNA_ID_1003708,Human_miRNA_ID_1266919,Human_miRNA_ID_1973121,Human_miRNA_ID_1973122,Human_miRNA_ID_1975298,Human_miRNA_ID_1975299,Human_miRNA_ID_2613102,Human_miRNA_ID_2613103 RMVar_hsa_circ_124468,RMVar_hsa_circ_147361,RMVar_hsa_circ_80540,RMVar_hsa_circ_125066,RMVar_hsa_circ_147367,RMVar_hsa_circ_147368 57620 RMVar_ID_57620 Human_SNP_ID_452862086 m1A Human chr11 - 289269 289255 289269 GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGGAGCTGCGGGGCGGGGGCCTCTGGGACTCACCGC GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGG______________GGCCTCTGGGACTCACCGC CCCCGCCCCGCAGCT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:289176..289412 26863410 MeRIP-seq:(Medium) rs1175275999 Functional Loss DEL dbSNP153 33..46 33 - - - 57621 RMVar_ID_57621 Human_SNP_ID_452862090 m1A Human chr11 - 289269 289263 289269 GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGGAGCTGCGGGGCGGGGGCCTCTGGGACTCACCGC GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGG______GGGGCGGGGGCCTCTGGGACTCACCGC CGCAGCT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:289176..289412 26863410 MeRIP-seq:(Medium) rs1274849718 Functional Loss DEL dbSNP153 33..38 33 - - - 57622 RMVar_ID_57622 Human_SNP_ID_452862093 m1A Human chr11 - 289269 289269 289269 GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGGAGCTGCGGGGCGGGGGCCTCTGGGACTCACCGC GGGGGCTGGGGGGACGGGCCGGGGCGGCCGGGGGCTGCGGGGCGGGGGCCTCTGGGACTCACCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:289176..289412 26863410 MeRIP-seq:(Medium) rs1252885687 Functional Loss SNV dbSNP153 33..33 33 - - - 57623 RMVar_ID_57623 Human_SNP_ID_452862192 m1A Human chr11 + 289541 289541 289541 GGGGTGCGTTTGGAAAGCAGGGTTAGGACTGGAATTCTAAGGTAGCAGGAGGGAGAGACACACTC GGGGTGCGTTTGGAAAGCAGGGTTAGGACTGGCATTCTAAGGTAGCAGGAGGGAGAGACACACTC A C PGGHG Ensembl:ENSG00000142102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:289498..289844 26863196 MeRIP-seq:(Medium) rs1314374165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259514,Human_RBP_ID_864669,Human_RBP_ID_3383724,Human_RBP_ID_3939976,Human_RBP_ID_5126087,Human_RBP_ID_8229008,Human_RBP_ID_11590266,Human_RBP_ID_17073883,Human_RBP_ID_21966352,Human_RBP_ID_22035019,Human_RBP_ID_22640735,Human_RBP_ID_23206780,Human_RBP_ID_24550998,Human_RBP_ID_26317907,Human_RBP_ID_26767841,Human_RBP_ID_26889292,Human_RBP_ID_27836215 57624 RMVar_ID_57624 Human_SNP_ID_452862851 m1A Human chr11 + 290959 290954 290960 AGAATGTGGCTTGGACGTGGTGGGGCCCCTGCAGCTGCGCCAGGCCCTGCGTGGCTCCCTCTACT AGAATGTGGCTTGGACGTGGTGGGGCCC______CTGCGCCAGGCCCTGCGTGGCTCCCTCTACT CCTGCAG C PGGHG Ensembl:ENSG00000142102 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:290908..291008 32194978 MeRIP-seq:(Medium) rs1362876235 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_32332,Human_RBP_ID_227672,Human_RBP_ID_751129,Human_RBP_ID_3938707,Human_RBP_ID_5167501,Human_RBP_ID_18159091,Human_RBP_ID_21965017,Human_RBP_ID_22035589,Human_RBP_ID_24363000 57625 RMVar_ID_57625 Human_SNP_ID_452862934 m1A Human chr11 + 291157 291157 291157 ACACCCAGCACCAGCCACACAGCAGGCGACACATGGAGGTCCACGGTCTCTGCCCTCCCTGGGAC ACACCCAGCACCAGCCACACAGCAGGCGACACGTGGAGGTCCACGGTCTCTGCCCTCCCTGGGAC A G PGGHG Ensembl:ENSG00000142102 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:291107..291356 32194978 MeRIP-seq:(Medium) rs370614850 Functional Loss SNV dbSNP153 33..33 33 - - - 57626 RMVar_ID_57626 Human_SNP_ID_452862987 m1A Human chr11 - 291320 291320 291320 GAGGCCCCTCCCCACGCTCTGGAAAGTGCCTCAGGCCCTCTCAGCTCTGGTCTCTGCACCTTCCA GAGGCCCCTCCCCACGCTCTGGAAAGTGCCTCGGGCCCTCTCAGCTCTGGTCTCTGCACCTTCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:291271..291605 26863196 MeRIP-seq:(Medium) rs549442826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6065404 57627 RMVar_ID_57627 Human_SNP_ID_452863035 m1A Human chr11 - 291487 291487 291487 GGCCTCCAGTACCGGGCTCCACGCAGCCCCACAGGCCTTCCCAGTCCCCACAGGTCCCCGTCCTG GGCCTCCAGTACCGGGCTCCACGCAGCCCCACGGGCCTTCCCAGTCCCCACAGGTCCCCGTCCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:291443..291605 26863196 MeRIP-seq:(Medium) rs1391877414 Functional Loss SNV dbSNP153 33..33 33 - - - 57628 RMVar_ID_57628 Human_SNP_ID_452869503 m1A Human chr11 + 308245 308245 308245 CTTCTCTCCTGTCAACAGCGGCCAGCCTCCCAACTACGAGATGCTCAAGGAGGAGCAGGAAGTGG CTTCTCTCCTGTCAACAGCGGCCAGCCTCCCAGCTACGAGATGCTCAAGGAGGAGCAGGAAGTGG A G IFITM2 Ensembl:ENSG00000185201 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:308151..308367 26863196 MeRIP-seq:(Medium) rs757104476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_869797,Human_RBP_ID_4184525,Human_RBP_ID_9321111,Human_RBP_ID_17681810,Human_RBP_ID_17804383,Human_RBP_ID_22432679 Human_Splice_Rec_1192602 RMVar_hsa_circ_80719,RMVar_hsa_circ_147371 57629 RMVar_ID_57629 Human_SNP_ID_452869881 m1A Human chr11 - 309177 309177 309177 ACAGGTCACGGGCAGAGCTCCTGGCCTCAATGATGCCTCCTGATCTATCGCTGGGCCTGGACGAC ACAGGTCACGGGCAGAGCTCCTGGCCTCAATGGTGCCTCCTGATCTATCGCTGGGCCTGGACGAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:309126..309275;chr11:309126..309298 32194978 MeRIP-seq:(Medium) rs754905614 Functional Loss SNV dbSNP153 33..33 33 - - - 57630 RMVar_ID_57630 Human_SNP_ID_452872820 m1A Human chr11 + 319776 319776 319776 GACTCGGCTCCGGGGGCAGGGCGAGGAATGGAAGTTGGAGTACGTGGGATACAGGTCATGGGCAG GACTCGGCTCCGGGGGCAGGGCGAGGAATGGACGTTGGAGTACGTGGGATACAGGTCATGGGCAG A C AC136475.1 Ensembl:ENSG00000251661 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:319676..319950;chr11:319676..319914 26863196 MeRIP-seq:(Medium) rs1166426553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3388428,Human_RBP_ID_5553059 57631 RMVar_ID_57631 Human_SNP_ID_452873202 m1A Human chr11 + 320697 320697 320697 CTGCGGATGTGGATCACGGTGGACGTCGGGGGAGCAGGGTTGTGGGGCGCCCCCAGCACAGCCAC CTGCGGATGTGGATCACGGTGGACGTCGGGGGCGCAGGGTTGTGGGGCGCCCCCAGCACAGCCAC A C AC136475.1 Ensembl:ENSG00000251661 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:320601..320875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5552515,Human_RBP_ID_8176609 57632 RMVar_ID_57632 Human_SNP_ID_452873203 m1A Human chr11 + 320697 320697 320697 CTGCGGATGTGGATCACGGTGGACGTCGGGGGAGCAGGGTTGTGGGGCGCCCCCAGCACAGCCAC CTGCGGATGTGGATCACGGTGGACGTCGGGGGGGCAGGGTTGTGGGGCGCCCCCAGCACAGCCAC A G AC136475.1 Ensembl:ENSG00000251661 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:320601..320875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5552515,Human_RBP_ID_8176609 57633 RMVar_ID_57633 Human_SNP_ID_452886169 m1A Human chr11 + 359963 359959 359963 AGAGACAGAGAGGGAAAGAGAGAGAAACGGAGAGAGAGAGACAGAGGGAGAGAGAGATGGGGGAG AGAGACAGAGAGGGAAAGAGAGAGAAACG____GAGAGAGACAGAGGGAGAGAGAGATGGGGGAG GGAGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:359674..360365 26863196 MeRIP-seq:(Medium) rs138055131 Functional Loss DEL dbSNP153 30..33 33 - - - 57634 RMVar_ID_57634 Human_SNP_ID_452886170 m1A Human chr11 + 359963 359959 359963 AGAGACAGAGAGGGAAAGAGAGAGAAACGGAGAGAGAGAGACAGAGGGAGAGAGAGATGGGGGAG AGAGACAGAGAGGGAAAGAGAGAGAAACGGA__GAGAGAGACAGAGGGAGAGAGAGATGGGGGAG GGAGA GGA - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:359674..360365 26863196 MeRIP-seq:(Medium) rs138055131 Functional Loss DEL dbSNP153 32..33 33 - - - 57635 RMVar_ID_57635 Human_SNP_ID_452890696 m1A Human chr11 - 372148 372148 372148 CCTCAGCCCTCTGTGTGGATGGCGCAGCGTGGACCCCCCGGCCGTCGGTCTCACTGGTCAGCTTC CCTCAGCCCTCTGTGTGGATGGCGCAGCGTGGGCCCCCCGGCCGTCGGTCTCACTGGTCAGCTTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:369943..372197 32194978 MeRIP-seq:(Medium) rs748055483 Functional Loss SNV dbSNP153 33..33 33 - - - 57636 RMVar_ID_57636 Human_SNP_ID_452890707 m1A Human chr11 - 372162 372162 372162 GCTCTCACTGGAGTCCTCAGCCCTCTGTGTGGATGGCGCAGCGTGGACCCCCCGGCCGTCGGTCT GCTCTCACTGGAGTCCTCAGCCCTCTGTGTGGGTGGCGCAGCGTGGACCCCCCGGCCGTCGGTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:369465..373147;chr11:369551..373125;chr11:369768..372696 26863196 MeRIP-seq:(Medium) rs1182237200 Functional Loss SNV dbSNP153 33..33 33 - - - 57637 RMVar_ID_57637 Human_SNP_ID_452891650 m1A Human chr11 + 374037 374037 374037 AGTCACCTTTGAGTAGAGTCTTGAGAGGATGGAGACCTTCAGTAGGGAGATGTGGGGGGCAGAGA AGTCACCTTTGAGTAGAGTCTTGAGAGGATGGGGACCTTCAGTAGGGAGATGTGGGGGGCAGAGA A G B4GALNT4 Ensembl:ENSG00000182272 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:374035..374139 26863196 MeRIP-seq:(Medium) rs533129386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113003,RMVar_hsa_circ_123144,RMVar_hsa_circ_147376,RMVar_hsa_circ_93861,RMVar_hsa_circ_147377,RMVar_hsa_circ_124448,RMVar_hsa_circ_147378,RMVar_hsa_circ_147379 57638 RMVar_ID_57638 Human_SNP_ID_452891776 m1A Human chr11 - 374393 374393 374393 CATCGTGCTGCCCCCCACACCCACCAGGCTGCAGGCCCTCTGCCTTGCTGTATAACCCCTTCCGC CATCGTGCTGCCCCCCACACCCACCAGGCTGCGGGCCCTCTGCCTTGCTGTATAACCCCTTCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:374386..374537 26863196 MeRIP-seq:(Medium) rs1051197968 Functional Loss SNV dbSNP153 33..33 33 - - - 57639 RMVar_ID_57639 Human_SNP_ID_452891784 m1A Human chr11 - 374409 374409 374409 CACCAGACACAGGCACCATCGTGCTGCCCCCCACACCCACCAGGCTGCAGGCCCTCTGCCTTGCT CACCAGACACAGGCACCATCGTGCTGCCCCCCCCACCCACCAGGCTGCAGGCCCTCTGCCTTGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:374407..374537 26863196 MeRIP-seq:(Medium) rs1445841217 Functional Loss SNV dbSNP153 33..33 33 - - - 57640 RMVar_ID_57640 Human_SNP_ID_452892320 m1A Human chr11 - 375513 375513 375513 AGAGGCGTCCGCTCGCACCTGTGTACAGGGAGATGTGAGCAGAGCTGATGACCTCGAACTTCAGG AGAGGCGTCCGCTCGCACCTGTGTACAGGGAGTTGTGAGCAGAGCTGATGACCTCGAACTTCAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:375371..375527 26863196 MeRIP-seq:(Medium) rs1404405283 Functional Loss SNV dbSNP153 33..33 33 - - - 57641 RMVar_ID_57641 Human_SNP_ID_452893035 m1A Human chr11 + 376653 376653 376653 GCCGCCCGCCCTTTGCCGCTCTTCTTGGGCCGAGCTCCGCCCCCGCGCCCTGCAGTGGAGCAGCC GCCGCCCGCCCTTTGCCGCTCTTCTTGGGCCGTGCTCCGCCCCCGCGCCCTGCAGTGGAGCAGCC A T B4GALNT4 Ensembl:ENSG00000182272 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:376604..376780 26863196 MeRIP-seq:(Medium) rs1363510019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395974,Human_RBP_ID_5344582,Human_RBP_ID_9321115,Human_RBP_ID_22034115,Human_RBP_ID_22432690 Human_miRNA_ID_2250109,Human_miRNA_ID_2386822,Human_miRNA_ID_2388299,Human_miRNA_ID_2399448,Human_miRNA_ID_3030502 RMVar_hsa_circ_113003,RMVar_hsa_circ_123144,RMVar_hsa_circ_147376,RMVar_hsa_circ_93861,RMVar_hsa_circ_147377,RMVar_hsa_circ_124448,RMVar_hsa_circ_147378,RMVar_hsa_circ_147379,RMVar_hsa_circ_147380,RMVar_hsa_circ_81445,RMVar_hsa_circ_109368,RMVar_hsa_circ_147382 57642 RMVar_ID_57642 Human_SNP_ID_452893037 m1A Human chr11 - 376656 376656 376656 GGCGGCTGCTCCACTGCAGGGCGCGGGGGCGGAGCTCGGCCCAAGAAGAGCGGCAAAGGGCGGGC GGCGGCTGCTCCACTGCAGGGCGCGGGGGCGGGGCTCGGCCCAAGAAGAGCGGCAAAGGGCGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:376243..376953 26863196 MeRIP-seq:(Medium) rs755853527 Functional Loss SNV dbSNP153 33..33 33 - - - 57643 RMVar_ID_57643 Human_SNP_ID_452893061 m1A Human chr11 + 376694 376694 376694 CCCGCGCCCTGCAGTGGAGCAGCCGCCCCCAAAGGTGTACGTGACCAGGGTGCGGCCGGGACAGC CCCGCGCCCTGCAGTGGAGCAGCCGCCCCCAATGGTGTACGTGACCAGGGTGCGGCCGGGACAGC A T B4GALNT4 Ensembl:ENSG00000182272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:376580..376800 26863196 MeRIP-seq:(Medium) rs1233562718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395974,Human_RBP_ID_22432690 RMVar_hsa_circ_113003,RMVar_hsa_circ_123144,RMVar_hsa_circ_147376,RMVar_hsa_circ_93861,RMVar_hsa_circ_147377,RMVar_hsa_circ_124448,RMVar_hsa_circ_147378,RMVar_hsa_circ_147379,RMVar_hsa_circ_147380,RMVar_hsa_circ_81445,RMVar_hsa_circ_109368,RMVar_hsa_circ_147382 57644 RMVar_ID_57644 Human_SNP_ID_452893392 m1A Human chr11 - 377329 377329 377329 AACCGCCCTGGCGCGCGTTCGGCCGCCCCCATACCCGCCGTGGCGCGCGTTCAGCCGCTCCATGT AACCGCCCTGGCGCGCGTTCGGCCGCCCCCATCCCCGCCGTGGCGCGCGTTCAGCCGCTCCATGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:377303..377404;chr11:377300..377397 26863196 MeRIP-seq:(Medium) rs373329286 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57645 RMVar_ID_57645 Human_SNP_ID_452893447 m1A Human chr11 - 377437 377437 377437 GGGGCGCGGTGCCTCAGCCCCCAGGCCGGTACACCACTGGGCCCTGGGGAAGGTCTGAGGAGTCC GGGGCGCGGTGCCTCAGCCCCCAGGCCGGTACGCCACTGGGCCCTGGGGAAGGTCTGAGGAGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:377433..377568 32194978 MeRIP-seq:(Medium) rs61876284 Functional Loss SNV dbSNP153 33..33 33 - - - 57646 RMVar_ID_57646 Human_SNP_ID_452893679 m1A Human chr11 - 378138 378138 378138 TGCCCCTGCCTTTGCTCTGCTCGCAACCTTCCATCACACACATGAGAAACAGTCCTGGCCCTGTC TGCCCCTGCCTTTGCTCTGCTCGCAACCTTCCGTCACACACATGAGAAACAGTCCTGGCCCTGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:377959..378357 26863196 MeRIP-seq:(Medium) rs1422849845 Functional Loss SNV dbSNP153 33..33 33 - - - 57647 RMVar_ID_57647 Human_SNP_ID_452893760 m1A Human chr11 - 378448 378448 378448 ACTGTTGCTCCTTGAGCCATACCCAGGTGGGCATTGGTGGGGCCACAACCATGATCTTCCCATGA ACTGTTGCTCCTTGAGCCATACCCAGGTGGGCGTTGGTGGGGCCACAACCATGATCTTCCCATGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:378446..379011 26863196 MeRIP-seq:(Medium) rs981791195 Functional Loss SNV dbSNP153 33..33 33 - - - 57648 RMVar_ID_57648 Human_SNP_ID_452893946 m1A Human chr11 + 379130 379130 379130 TTCTGAGCAAGGGGGTAACAGGACAGGCGGGCATGTCATAAACGTCACCTGGGACGTGAGTGGTG TTCTGAGCAAGGGGGTAACAGGACAGGCGGGCGTGTCATAAACGTCACCTGGGACGTGAGTGGTG A G B4GALNT4 Ensembl:ENSG00000182272 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:379116..379269 26863196 MeRIP-seq:(Medium) rs1183970631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113003,RMVar_hsa_circ_123144,RMVar_hsa_circ_147376,RMVar_hsa_circ_93861,RMVar_hsa_circ_147377,RMVar_hsa_circ_124448,RMVar_hsa_circ_147378,RMVar_hsa_circ_147379,RMVar_hsa_circ_147380,RMVar_hsa_circ_81445,RMVar_hsa_circ_109368,RMVar_hsa_circ_147382 57649 RMVar_ID_57649 Human_SNP_ID_452893947 m1A Human chr11 - 379133 379133 379133 GGCCACCACTCACGTCCCAGGTGACGTTTATGACATGCCCGCCTGTCCTGTTACCCCCTTGCTCA GGCCACCACTCACGTCCCAGGTGACGTTTATGTCATGCCCGCCTGTCCTGTTACCCCCTTGCTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:379123..379251 26863196 MeRIP-seq:(Medium) rs1041565435 Functional Loss SNV dbSNP153 33..33 33 - - - 57650 RMVar_ID_57650 Human_SNP_ID_452894128 m1A Human chr11 - 379604 379604 379604 GGGCGGCCGTCGGGGCGCACGGAGGCGGCGGGAGCGGGTTCGGGACTTTCTCCGTCTGCATCCCC GGGCGGCCGTCGGGGCGCACGGAGGCGGCGGGGGCGGGTTCGGGACTTTCTCCGTCTGCATCCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:379411..379633 26863196 MeRIP-seq:(Medium) rs1313431269 Functional Loss SNV dbSNP153 33..33 33 - - - 57651 RMVar_ID_57651 Human_SNP_ID_452897715 m1A Human chr11 - 391677 391677 391677 TGGGCTCAGCGTGGGGGGCACGGGAGGCGCTCACAGAGAAGGTCGGCTGGGCCCAGGTCGTGGGC TGGGCTCAGCGTGGGGGGCACGGGAGGCGCTCCCAGAGAAGGTCGGCTGGGCCCAGGTCGTGGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:391438..391844 26863196 MeRIP-seq:(Medium) rs1263350655 Functional Loss SNV dbSNP153 33..33 33 - - - 57652 RMVar_ID_57652 Human_SNP_ID_452898616 m1A Human chr11 - 394251 394251 394251 TCCACCGGGCCTGGGCCTGGCGGCCGCCTCCAAACCCAACTATCTTCACGTCCTGTCCCTCGAGG TCCACCGGGCCTGGGCCTGGCGGCCGCCTCCATACCCAACTATCTTCACGTCCTGTCCCTCGAGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:394201..394444 26863196 MeRIP-seq:(Medium) rs1465190812 Functional Loss SNV dbSNP153 33..33 33 - - - 57653 RMVar_ID_57653 Human_SNP_ID_452898724 m1A Human chr11 + 394466 394466 394466 GAGCAGGTCCGCGCCCGCCTCTTGCAGCTGGGACAGCAGCCGCGGCACAACGGGGCCGCTGAGCC GAGCAGGTCCGCGCCCGCCTCTTGCAGCTGGGGCAGCAGCCGCGGCACAACGGGGCCGCTGAGCC A G PKP3 Ensembl:ENSG00000184363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:394345..396171 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4184531,Human_RBP_ID_24551021 Human_Splice_Rec_1192717,Human_Splice_Rec_1192723,Human_Splice_Rec_1192731,Human_Splice_Rec_1192737,Human_Splice_Rec_1192741,Human_Splice_Rec_1192765,Human_Splice_Rec_1192767 RMVar_hsa_circ_126824,RMVar_hsa_circ_147386 57654 RMVar_ID_57654 Human_SNP_ID_452898725 m1A Human chr11 + 394466 394466 394466 GAGCAGGTCCGCGCCCGCCTCTTGCAGCTGGGACAGCAGCCGCGGCACAACGGGGCCGCTGAGCC GAGCAGGTCCGCGCCCGCCTCTTGCAGCTGGGTCAGCAGCCGCGGCACAACGGGGCCGCTGAGCC A T PKP3 Ensembl:ENSG00000184363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:394345..396171 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4184531,Human_RBP_ID_24551021 Human_Splice_Rec_1192717,Human_Splice_Rec_1192723,Human_Splice_Rec_1192731,Human_Splice_Rec_1192737,Human_Splice_Rec_1192741,Human_Splice_Rec_1192765,Human_Splice_Rec_1192767 RMVar_hsa_circ_126824,RMVar_hsa_circ_147386 57655 RMVar_ID_57655 Human_SNP_ID_452899599 m1A Human chr11 + 396995 396995 396995 CCCTCCCATGCCCACCAGGCCCGTGTCCTTCCATGAGCGCGGTGGGGTTGGGAGCCGGGCCGACT CCCTCCCATGCCCACCAGGCCCGTGTCCTTCCGTGAGCGCGGTGGGGTTGGGAGCCGGGCCGACT A G PKP3 Ensembl:ENSG00000184363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:396837..397186 32194978 MeRIP-seq:(Medium) rs1403515472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773286,Human_RBP_ID_9276189 RMVar_hsa_circ_126824,RMVar_hsa_circ_78494,RMVar_hsa_circ_147386,RMVar_hsa_circ_147387 57656 RMVar_ID_57656 Human_SNP_ID_452900623 m1A Human chr11 - 399089 399089 399089 CCAGGGCCAGCTTGTTGTCAGCGTTGTCGTAGATGAGGTTGCGCATGGCACCTGTGGCATGGCGC CCAGGGCCAGCTTGTTGTCAGCGTTGTCGTAGGTGAGGTTGCGCATGGCACCTGTGGCATGGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:399039..399128 26863196 MeRIP-seq:(Medium) rs764290617 Functional Loss SNV dbSNP153 33..33 33 - - - 57657 RMVar_ID_57657 Human_SNP_ID_452901326 m1A Human chr11 - 400402 400402 400402 CCGCGTCCAGGGCGTGGTTGATAGAGGTGACCAGGGCGTCCACCAGCCCGTGGCACTCCCGCATC CCGCGTCCAGGGCGTGGTTGATAGAGGTGACCCGGGCGTCCACCAGCCCGTGGCACTCCCGCATC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:400212..400450 26863196 MeRIP-seq:(Medium) rs762855127 Functional Loss SNV dbSNP153 33..33 33 - - - 57658 RMVar_ID_57658 Human_SNP_ID_452901341 m1A Human chr11 - 400426 400426 400426 CCCTCACCTTGTCCTCGCATTTGCCCGCGTCCAGGGCGTGGTTGATAGAGGTGACCAGGGCGTCC CCCTCACCTTGTCCTCGCATTTGCCCGCGTCCGGGGCGTGGTTGATAGAGGTGACCAGGGCGTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:400376..400725 26863196 MeRIP-seq:(Medium) rs1007484732 Functional Loss SNV dbSNP153 33..33 33 - - - 57659 RMVar_ID_57659 Human_SNP_ID_452901464 m1A Human chr11 - 400601 400587 400602 GCGGCCGCGACCCTCCAGCCGCTGCAGCGCGGACGGCGGCATCTCGTCGTAGAGGCGGTAGGACA GCGGCCGCGACCCTCCAGCCGCTGCAGCGCG_______________TCGTAGAGGCGGTAGGACA ACGAGATGCCGCCGTC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:400551..400600 26863196 MeRIP-seq:(Medium) rs1165292304 Functional Loss DEL dbSNP153 32..46 33 - - - 57660 RMVar_ID_57660 Human_SNP_ID_452902626 m1A Human chr11 + 403120 403120 403120 CCGCCGATGCGCTCACCTTCGCGGAGGTGTCCAAGGACCCCAAGGGCCTCGAGTGGCTGTGGAGC CCGCCGATGCGCTCACCTTCGCGGAGGTGTCCGAGGACCCCAAGGGCCTCGAGTGGCTGTGGAGC A G PKP3 Ensembl:ENSG00000184363 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:403022..403203 26863196 MeRIP-seq:(Medium) rs771899111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5234868,Human_RBP_ID_18972987,Human_RBP_ID_22432693 Human_Splice_Rec_1192756 RMVar_hsa_circ_121041,RMVar_hsa_circ_126824,RMVar_hsa_circ_78494,RMVar_hsa_circ_147386,RMVar_hsa_circ_147387,RMVar_hsa_circ_122075,RMVar_hsa_circ_147388,RMVar_hsa_circ_147389,RMVar_hsa_circ_147390,RMVar_hsa_circ_85832 57661 RMVar_ID_57661 Human_SNP_ID_452903798 m1A Human chr11 - 405866 405866 405866 TAGCTCCCACCCCAGAGTGCAGGATCATAGGGACAGCGGGGGCCAGGGCAGCGGCGTCGCTCCTC TAGCTCCCACCCCAGAGTGCAGGATCATAGGGTCAGCGGGGGCCAGGGCAGCGGCGTCGCTCCTC T A SIGIRR Ensembl:ENSG00000185187 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:405815..405990 26863196 MeRIP-seq:(Medium) rs1293358342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396089,Human_RBP_ID_5110681,Human_RBP_ID_27201316 Human_miRNA_ID_3090540 RMVar_hsa_circ_111377,RMVar_hsa_circ_147392 57662 RMVar_ID_57662 Human_SNP_ID_452904167 m1A Human chr11 - 406540 406540 406540 TCACACCTGCAAACCGCCCCGACCTGGCCCCCAGACTCCTTCCTCCGATTTTTGGAAAGAAGTGC TCACACCTGCAAACCGCCCCGACCTGGCCCCCGGACTCCTTCCTCCGATTTTTGGAAAGAAGTGC T C SIGIRR Ensembl:ENSG00000185187 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:406514..406765 26863196 MeRIP-seq:(Medium) rs1411070214 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57663 RMVar_ID_57663 Human_SNP_ID_452904336 m1A Human chr11 + 406949 406948 406949 CGGGGTCGCGCCTCTGGCCCTCGAAGGTGATGAAGATGGGTCTGCGGGTGAGCTCCAGCAGCCGG CGGGGTCGCGCCTCTGGCCCTCGAAGGTGATG_AGATGGGTCTGCGGGTGAGCTCCAGCAGCCGG GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:406838..407125 26863196 MeRIP-seq:(Medium) rs1564887281 Functional Loss DEL dbSNP153 33..33 33 - - - 57664 RMVar_ID_57664 Human_SNP_ID_452904439 m1A Human chr11 + 407110 407110 407110 ACCAGGCCCGGCTCAGGAAGGCGTCCGAAAGCACCACGATGAGGCGTCGGCAGCGGCTCAGGTTC ACCAGGCCCGGCTCAGGAAGGCGTCCGAAAGCTCCACGATGAGGCGTCGGCAGCGGCTCAGGTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:406770..407164;chr11:406778..407114;chr11:406764..407164 26863196 MeRIP-seq:(Medium) rs1368470503 Functional Loss SNV dbSNP153 33..33 33 - - - 57665 RMVar_ID_57665 Human_SNP_ID_452906694 m1A Human chr11 + 412727 412727 412727 TGCCCAGCTCTAACCATGTCTGGATGCAGTCGAGGGGGGGTGCCCAGCTCTGGCCCACGTCTGGT TGCCCAGCTCTAACCATGTCTGGATGCAGTCGGGGGGGGGTGCCCAGCTCTGGCCCACGTCTGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:412721..412805 26863196 MeRIP-seq:(Medium) rs534422775 Functional Loss SNV dbSNP153 33..33 33 - - - 57666 RMVar_ID_57666 Human_SNP_ID_452908973 m1A Human chr11 - 419836 419836 419836 TGAATACTGCAGCCCTAGGGCTGCAAGGGGACACCACGCACAGAGACACGGCAGGCCCCGTGTTG TGAATACTGCAGCCCTAGGGCTGCAAGGGGACGCCACGCACAGAGACACGGCAGGCCCCGTGTTG T C ANO9 Ensembl:ENSG00000185101 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:419833..420129 26863196 MeRIP-seq:(Medium) rs910488638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89001,RMVar_hsa_circ_147395 57667 RMVar_ID_57667 Human_SNP_ID_452910652 m1A Human chr11 + 425258 425235 425259 AAAAGGCGGCGTGGAGAGACGGGACGCGCGGGAGCAAAAGGCGGCGTGGAGAGACGGGACGCGCG AAAAGGCGGC________________________CAAAAGGCGGCGTGGAGAGACGGGACGCGCG CGTGGAGAGACGGGACGCGCGGGAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:425215..425381 26863196 MeRIP-seq:(Medium) rs1346189078 Functional Loss DEL dbSNP153 11..34 33 - - - 57668 RMVar_ID_57668 Human_SNP_ID_452914939 m1A Human chr11 - 436658 436658 436658 CCTCCTGCTCACTCCCTGCTCACTCCCTGCTCACCCCCTGCTCACCTCCTGCTCACTCCCTGCTC CCTCCTGCTCACTCCCTGCTCACTCCCTGCTCCCCCCCTGCTCACCTCCTGCTCACTCCCTGCTC T G ANO9 Ensembl:ENSG00000185101 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:436551..436679 26863196 MeRIP-seq:(Medium) rs1422753847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3384586,Human_RBP_ID_18932067 57669 RMVar_ID_57669 Human_SNP_ID_452919164 m1A Human chr11 + 450462 450462 450462 GCGGAGTGGCTCCGGGCCGAAACGCCATGCGGAGGGGCGAGCGCAGGGACGCCGGAGGTCCGCGG GCGGAGTGGCTCCGGGCCGAAACGCCATGCGGCGGGGCGAGCGCAGGGACGCCGGAGGTCCGCGG A C PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:450337..450590 26863196 MeRIP-seq:(Medium) rs751369515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4183865,Human_RBP_ID_9321839,Human_RBP_ID_18188408,Human_RBP_ID_18410451,Human_RBP_ID_22433329 57670 RMVar_ID_57670 Human_SNP_ID_452919171 m1A Human chr11 + 450485 450485 450485 GCCATGCGGAGGGGCGAGCGCAGGGACGCCGGAGGTCCGCGGCCCGAGTCCCCGGTGCCCGCGGG GCCATGCGGAGGGGCGAGCGCAGGGACGCCGGGGGTCCGCGGCCCGAGTCCCCGGTGCCCGCGGG A G PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:450305..450625;chr11:450326..450589;chr11:450325..450625 26863196 MeRIP-seq:(Medium) rs182480820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4183865,Human_RBP_ID_18410451,Human_RBP_ID_22433329 57671 RMVar_ID_57671 Human_SNP_ID_452924553 m1A Human chr11 + 468760 468757 468760 AGAAGGAGGGGAGTCTCTGGGTAATCAGAGGGAGGAGGAGGGGAGTCTCTGGGTAATTGGAGGAG AGAAGGAGGGGAGTCTCTGGGTAATCAGAG___GGAGGAGGGGAGTCTCTGGGTAATTGGAGGAG GGGA G PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:468754..469287 26863196 MeRIP-seq:(Medium) rs1248894922 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23506800 RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 57672 RMVar_ID_57672 Human_SNP_ID_452924554 m1A Human chr11 + 468760 468760 468760 AGAAGGAGGGGAGTCTCTGGGTAATCAGAGGGAGGAGGAGGGGAGTCTCTGGGTAATTGGAGGAG AGAAGGAGGGGAGTCTCTGGGTAATCAGAGGGTGGAGGAGGGGAGTCTCTGGGTAATTGGAGGAG A T PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:468754..469287 26863196 MeRIP-seq:(Medium) rs1210883493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23506800 RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 57673 RMVar_ID_57673 Human_SNP_ID_452924585 m1A Human chr11 + 468844 468842 468844 GAGGAGGGGAGTCTGGGTAATCGGAGGAGGGGAGTCTCTGAGATGGAGGGGAGTCTCTGAATAAT GAGGAGGGGAGTCTGGGTAATCGGAGGAGGG__GTCTCTGAGATGGAGGGGAGTCTCTGAATAAT GGA G PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:468833..469061 26863196 MeRIP-seq:(Medium) rs1564972261 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8173845,Human_RBP_ID_22568291 RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 57674 RMVar_ID_57674 Human_SNP_ID_452924687 m1A Human chr11 + 469140 469140 469140 AGTCTCTGGGTAATCGGAAGGAGGAGGAGGGGAGTCTCTGGGTAATTGGAAGGAGGAGGAGGGCA AGTCTCTGGGTAATCGGAAGGAGGAGGAGGGGGGTCTCTGGGTAATTGGAAGGAGGAGGAGGGCA A G PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:469134..469256 26863196 MeRIP-seq:(Medium) rs1436140060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 57675 RMVar_ID_57675 Human_SNP_ID_452925566 m1A Human chr11 + 471991 471991 471991 GGTGATGCAGATGGCGGCCTGGGGTGACGCGGATGGCGGCCTGGGGTGACGCGGATGGCGGCCTG GGTGATGCAGATGGCGGCCTGGGGTGACGCGGCTGGCGGCCTGGGGTGACGCGGATGGCGGCCTG A C PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:471676..472103 26863196 MeRIP-seq:(Medium) rs1332039541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8063781,Human_RBP_ID_8173849 RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 57676 RMVar_ID_57676 Human_SNP_ID_452933641 m1A Human chr11 - 494719 494719 494719 GATGGAGGACCGGCTGCAGGCCCTGGAGAAGGACAAGCCATCCCTGAGGGTCATCTCCTGAGGCT GATGGAGGACCGGCTGCAGGCCCTGGAGAAGGGCAAGCCATCCCTGAGGGTCATCTCCTGAGGCT T C RNH1 Ensembl:ENSG00000023191 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:494593..494858 26863196 MeRIP-seq:(Medium) rs1005195425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17804387,Human_RBP_ID_22432696 Human_Splice_Rec_1193264,Human_Splice_Rec_1193282,Human_Splice_Rec_1193302,Human_Splice_Rec_1193322,Human_Splice_Rec_1193340,Human_Splice_Rec_1193356,Human_Splice_Rec_1193374,Human_Splice_Rec_1193400,Human_Splice_Rec_1193418,Human_Splice_Rec_1193436 Human_miRNA_ID_2043156,Human_miRNA_ID_2043157,Human_miRNA_ID_2045307,Human_miRNA_ID_2045308,Human_miRNA_ID_2254894,Human_miRNA_ID_2254895 RMVar_hsa_circ_121889,RMVar_hsa_circ_126827,RMVar_hsa_circ_123276,RMVar_hsa_circ_147408,RMVar_hsa_circ_105401,RMVar_hsa_circ_117423,RMVar_hsa_circ_147410,RMVar_hsa_circ_103043,RMVar_hsa_circ_147409,RMVar_hsa_circ_147406,RMVar_hsa_circ_147407,RMVar_hsa_circ_147405 57677 RMVar_ID_57677 Human_SNP_ID_452933668 m1A Human chr11 + 494765 494765 494765 CTGCAGCCGGTCCTCCATCTCCTCAGACCAGTAAATGTCGTACAGGCTGCACACAGGCCAGAAGG CTGCAGCCGGTCCTCCATCTCCTCAGACCAGTTAATGTCGTACAGGCTGCACACAGGCCAGAAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:494551..494811 32194978 MeRIP-seq:(Medium) rs1022792844 Functional Loss SNV dbSNP153 33..33 33 - - - 57678 RMVar_ID_57678 Human_SNP_ID_452933809 m1A Human chr11 - 495005 495005 495005 GTGAGTGACAGCAGCTGCAGCAGCCTCGCCGCAACCCTGTTGGCCAACCACAGCCTGCGTGAGCT GTGAGTGACAGCAGCTGCAGCAGCCTCGCCGCGACCCTGTTGGCCAACCACAGCCTGCGTGAGCT T C RNH1 Ensembl:ENSG00000023191 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:494959..495088 26863196 MeRIP-seq:(Medium) rs1436199021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5110319,Human_RBP_ID_5138792,Human_RBP_ID_18188107,Human_RBP_ID_22432698,Human_RBP_ID_22753231,Human_RBP_ID_26803053 Human_Splice_Rec_1193262,Human_Splice_Rec_1193280,Human_Splice_Rec_1193300,Human_Splice_Rec_1193320,Human_Splice_Rec_1193338,Human_Splice_Rec_1193354,Human_Splice_Rec_1193372,Human_Splice_Rec_1193380,Human_Splice_Rec_1193398,Human_Splice_Rec_1193416,Human_Splice_Rec_1193434,Human_Splice_Rec_1193444 Human_miRNA_ID_2294038,Human_miRNA_ID_2294039 RMVar_hsa_circ_121889,RMVar_hsa_circ_126827,RMVar_hsa_circ_123276,RMVar_hsa_circ_147408,RMVar_hsa_circ_117423,RMVar_hsa_circ_103043,RMVar_hsa_circ_147409,RMVar_hsa_circ_147406,RMVar_hsa_circ_147407,RMVar_hsa_circ_147405 57679 RMVar_ID_57679 Human_SNP_ID_452935688 m1A Human chr11 - 499081 499081 499081 CAAGGAGCTCACGGTTAGCAACAACGACATCAATGAGGCTGGCGTCCGTGTGCTGTGCCAGGGCC CAAGGAGCTCACGGTTAGCAACAACGACATCAGTGAGGCTGGCGTCCGTGTGCTGTGCCAGGGCC T C RNH1 Ensembl:ENSG00000023191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:498802..499200 26863196 MeRIP-seq:(Medium) rs763265221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1457434,Human_RBP_ID_4162658,Human_RBP_ID_17796910,Human_RBP_ID_22491296 Human_Splice_Rec_1193255,Human_Splice_Rec_1193273,Human_Splice_Rec_1193293,Human_Splice_Rec_1193313,Human_Splice_Rec_1193331,Human_Splice_Rec_1193347,Human_Splice_Rec_1193365,Human_Splice_Rec_1193391,Human_Splice_Rec_1193409,Human_Splice_Rec_1193427,Human_Splice_Rec_1193453 Human_miRNA_ID_2397678,Human_miRNA_ID_2397679 RMVar_hsa_circ_14107,RMVar_hsa_circ_123276,RMVar_hsa_circ_117423,RMVar_hsa_circ_103043,RMVar_hsa_circ_147406,RMVar_hsa_circ_147407,RMVar_hsa_circ_147405 57680 RMVar_ID_57680 Human_SNP_ID_452935877 m1A Human chr11 + 499508 499508 499508 GCTGTGGTCAACTCACAATGGCCGGGTCCCCCACACACACTGAGGCGGTGAGTGGAACCTGACTC GCTGTGGTCAACTCACAATGGCCGGGTCCCCCCCACACACTGAGGCGGTGAGTGGAACCTGACTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:499503..499704 32194978 MeRIP-seq:(Medium) rs1489090982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27412032 57681 RMVar_ID_57681 Human_SNP_ID_452936375 m1A Human chr11 + 500642 500640 500642 CTGATGTCCTTGCACCGTGCTTCCGTGAGGCCACAGTCGTCCAGCCTGTGAGCAGACCCCAGGGT CTGATGTCCTTGCACCGTGCTTCCGTGAGGC__CAGTCGTCCAGCCTGTGAGCAGACCCCAGGGT CCA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:500476..500700;chr11:500476..500675 32194978 MeRIP-seq:(Medium) rs1212137018 Functional Loss DEL dbSNP153 32..33 33 - - - 57682 RMVar_ID_57682 Human_SNP_ID_452937567 m1A Human chr11 + 504522 504522 504522 CGGGCGGAGCCTCCAGGCCGGGGCTGGCGGGGAGTCCACCCTGGGGGCCGCGCCCGCTAGTCGTC CGGGCGGAGCCTCCAGGCCGGGGCTGGCGGGGGGTCCACCCTGGGGGCCGCGCCCGCTAGTCGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:504515..504791 26863196 MeRIP-seq:(Medium) rs976718704 Functional Loss SNV dbSNP153 33..33 33 - - - 57683 RMVar_ID_57683 Human_SNP_ID_452937663 m1A Human chr11 + 504829 504829 504829 TTGCCCAAACAATAAAATAAAGCAAACCTGAGACACCCCTTTTTGCTACCAGACTGGAGAAGGTG TTGCCCAAACAATAAAATAAAGCAAACCTGAGTCACCCCTTTTTGCTACCAGACTGGAGAAGGTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:504826..505000 32194978 MeRIP-seq:(Medium) rs966680256 Functional Loss SNV dbSNP153 33..33 33 - - - 57684 RMVar_ID_57684 Human_SNP_ID_452937673 m1A Human chr11 + 504856 504856 504856 CTGAGACACCCCTTTTTGCTACCAGACTGGAGAAGGTGGAACAGGTTGACGATGATTTGTTGTAG CTGAGACACCCCTTTTTGCTACCAGACTGGAGCAGGTGGAACAGGTTGACGATGATTTGTTGTAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:504854..504955 26863196 MeRIP-seq:(Medium) rs1405498099 Functional Loss SNV dbSNP153 33..33 33 - - - 57685 RMVar_ID_57685 Human_SNP_ID_452947651 m1A Human chr11 - 534329 534327 534329 CCTGTAGGAGGACCCCGGGCCGCAGGCCCCTGAGGAGCGATGACGGAATATAAGCTGGTGGTGGT CCTGTAGGAGGACCCCGGGCCGCAGGCCCCTG__GAGCGATGACGGAATATAAGCTGGTGGTGGT CCT C HRAS Ensembl:ENSG00000174775 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:533838..535550 26863196 MeRIP-seq:(Medium) rs772989900 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_259346,Human_RBP_ID_750462,Human_RBP_ID_4162748,Human_RBP_ID_5313450,Human_RBP_ID_23508461 Human_Splice_Rec_1193538,Human_Splice_Rec_1193546,Human_Splice_Rec_1193558,Human_Splice_Rec_1193568,Human_Splice_Rec_1193578,Human_Splice_Rec_1193596,Human_Splice_Rec_1193600 RMVar_hsa_circ_118031,RMVar_hsa_circ_147412 57686 RMVar_ID_57686 Human_SNP_ID_452947678 m1A Human chr11 - 534353 534353 534353 TCCTTGGCAGGTGGGGCAGGAGACCCTGTAGGAGGACCCCGGGCCGCAGGCCCCTGAGGAGCGAT TCCTTGGCAGGTGGGGCAGGAGACCCTGTAGGGGGACCCCGGGCCGCAGGCCCCTGAGGAGCGAT T C HRAS Ensembl:ENSG00000174775 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:534178..534432 26863196 MeRIP-seq:(Medium) rs1169813174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259346,Human_RBP_ID_750462,Human_RBP_ID_3938766,Human_RBP_ID_4184543,Human_RBP_ID_5313450,Human_RBP_ID_22537183,Human_RBP_ID_23508462 Human_Splice_Rec_1193538,Human_Splice_Rec_1193546,Human_Splice_Rec_1193558,Human_Splice_Rec_1193568,Human_Splice_Rec_1193578,Human_Splice_Rec_1193596,Human_Splice_Rec_1193600 RMVar_hsa_circ_118031,RMVar_hsa_circ_147412 57687 RMVar_ID_57687 Human_SNP_ID_452947937 m1A Human chr11 + 535023 535023 535023 GAGACCCGGAGAGGGAAAAGGCACTGGGGCTGAGGCCCCCGGCCTGGTCCGCGACCTGTGATGCT GAGACCCGGAGAGGGAAAAGGCACTGGGGCTGCGGCCCCCGGCCTGGTCCGCGACCTGTGATGCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:535021..535150 32194978 MeRIP-seq:(Medium) rs1218556104 Functional Loss SNV dbSNP153 33..33 33 - - - 57688 RMVar_ID_57688 Human_SNP_ID_452948204 m1A Human chr11 - 535504 535504 535504 AACCCGAGCCGCACCCGCCGCGGACGGAGCCCATGCGCGGGGCGAACCGCGCGCCCCCGCCCCCG AACCCGAGCCGCACCCGCCGCGGACGGAGCCCGTGCGCGGGGCGAACCGCGCGCCCCCGCCCCCG T C HRAS Ensembl:ENSG00000174775 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:535400..535569 26863410 MeRIP-seq:(Medium) rs1481423560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4162756,Human_RBP_ID_9321846 Human_Splice_Rec_1193545,Human_Splice_Rec_1193557,Human_Splice_Rec_1193567,Human_Splice_Rec_1193577 RMVar_hsa_circ_118031,RMVar_hsa_circ_147412 57689 RMVar_ID_57689 Human_SNP_ID_452953188 m1A Human chr11 + 550187 550186 550187 CAACAGCGTGGAGGACCTGGGGCAGGTGCGCTACTTGCAGCTGTGCCCACGCCTGGCCATGCTCA CAACAGCGTGGAGGACCTGGGGCAGGTGCGCT_CTTGCAGCTGTGCCCACGCCTGGCCATGCTCA TA T LRRC56 Ensembl:ENSG00000161328 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:550186..551144 32194978 MeRIP-seq:(Medium) rs777448469 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1193615 RMVar_hsa_circ_101086,RMVar_hsa_circ_147414,RMVar_hsa_circ_83831,RMVar_hsa_circ_147413 57690 RMVar_ID_57690 Human_SNP_ID_452955519 m1A Human chr11 + 555276 555276 555276 GAGAGGAGAGGAGGAGAACGAGGAGGGAGAGGAGGGGGCGCACCCGCAAGCGCGCACTCACCCGA GAGAGGAGAGGAGGAGAACGAGGAGGGAGAGGGGGGGGCGCACCCGCAAGCGCGCACTCACCCGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:555270..555893 26863196 MeRIP-seq:(Medium) rs1564813152 Functional Loss SNV dbSNP153 33..33 33 - - - 57691 RMVar_ID_57691 Human_SNP_ID_452955527 m1A Human chr11 + 555285 555285 555285 GGAGGAGAACGAGGAGGGAGAGGAGGGGGCGCACCCGCAAGCGCGCACTCACCCGAACTCGGTGT GGAGGAGAACGAGGAGGGAGAGGAGGGGGCGCCCCCGCAAGCGCGCACTCACCCGAACTCGGTGT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:555276..555527 26863196 MeRIP-seq:(Medium) rs373015093 Functional Loss SNV dbSNP153 33..33 33 - - - 57692 RMVar_ID_57692 Human_SNP_ID_452955829 m1A Human chr11 - 555855 555855 555855 CGAGGGTCTTCGCCGACGGCACCGACTTGTCCATCGACCGCTTCCCGCTCCCTGAGGCCGGGCCC CGAGGGTCTTCGCCGACGGCACCGACTTGTCCGTCGACCGCTTCCCGCTCCCTGAGGCCGGGCCC T C LMNTD2 Ensembl:ENSG00000185522 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:555821..555961 26863196 MeRIP-seq:(Medium) rs375199142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1193648,Human_Splice_Rec_1193656 57693 RMVar_ID_57693 Human_SNP_ID_452955989 m1A Human chr11 + 556112 556112 556112 CGGCTTCTTGGCGCTGCGGGTCGCCTCGCCCCAGACCTGGAGGGGCGTGGAGCGGCGGGTGAGGG CGGCTTCTTGGCGCTGCGGGTCGCCTCGCCCCTGACCTGGAGGGGCGTGGAGCGGCGGGTGAGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:556106..556898 32194978 MeRIP-seq:(Medium) rs1250459065 Functional Loss SNV dbSNP153 33..33 33 - - - 57694 RMVar_ID_57694 Human_SNP_ID_452958494 m1A Human chr11 - 561035 561035 561035 CGCTCCCAAGTACCGGGGACCCGGCGCGGCTCACCTGGGCGCTCGCCAGCCTGGAGACCCGCTCC CGCTCCCAAGTACCGGGGACCCGGCGCGGCTCCCCTGGGCGCTCGCCAGCCTGGAGACCCGCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:560985..561097 26863196 MeRIP-seq:(Medium) rs1442836339 Functional Loss SNV dbSNP153 33..33 33 - - - 57695 RMVar_ID_57695 Human_SNP_ID_452958710 m1A Human chr11 - 561562 561562 561562 GTGGCGGCCCTCCGGAGCACGCATCCTCCCCCACTTCACCAGCTTCCTCTTGCCACGCTCGCACT GTGGCGGCCCTCCGGAGCACGCATCCTCCCCCGCTTCACCAGCTTCCTCTTGCCACGCTCGCACT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:561541..561678 26863196 MeRIP-seq:(Medium) rs1341876904 Functional Loss SNV dbSNP153 33..33 33 - - - 57696 RMVar_ID_57696 Human_SNP_ID_452958856 m1A Human chr11 - 561813 561813 561813 TCTGAGACCCCACAGACCACACGCTGGATGCCATCCACCCACACCTTCAGCTCCATGGCCGCCAG TCTGAGACCCCACAGACCACACGCTGGATGCCTTCCACCCACACCTTCAGCTCCATGGCCGCCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:561169..561893;chr11:560979..561890 26863196 MeRIP-seq:(Medium) rs775043913 Functional Loss SNV dbSNP153 33..33 33 - - - 57697 RMVar_ID_57697 Human_SNP_ID_452958857 m1A Human chr11 - 561813 561813 561813 TCTGAGACCCCACAGACCACACGCTGGATGCCATCCACCCACACCTTCAGCTCCATGGCCGCCAG TCTGAGACCCCACAGACCACACGCTGGATGCCGTCCACCCACACCTTCAGCTCCATGGCCGCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:561169..561893;chr11:560979..561890 26863196 MeRIP-seq:(Medium) rs775043913 Functional Loss SNV dbSNP153 33..33 33 - - - 57698 RMVar_ID_57698 Human_SNP_ID_452959327 m1A Human chr11 - 562554 562554 562554 TCCAGGGCCTGCAGCCGGGCGGCATGCTCAGCAGTGGCCGCACTTAGTGCCTGCAGGCGTGCCTG TCCAGGGCCTGCAGCCGGGCGGCATGCTCAGCTGTGGCCGCACTTAGTGCCTGCAGGCGTGCCTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:562505..562667 26863196 MeRIP-seq:(Medium) rs944830019 Functional Loss SNV dbSNP153 33..33 33 - - - 57699 RMVar_ID_57699 Human_SNP_ID_452961414 m1A Human chr11 + 567543 567543 567543 CTCTCCCTCTCCAGCGAGCAGGTGCAGCCCTCAACTCCTGCAGGCCTGGGGAGCGGAGACAGGGC CTCTCCCTCTCCAGCGAGCAGGTGCAGCCCTCGACTCCTGCAGGCCTGGGGAGCGGAGACAGGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:567494..567637 26863196 MeRIP-seq:(Medium) rs758456566 Functional Loss SNV dbSNP153 33..33 33 - - - 57700 RMVar_ID_57700 Human_SNP_ID_452961420 m1A Human chr11 - 567577 567577 567577 TAAAATCAGGACCGGGTCGTGTCCGAGCCTACAGGCCCTGTCTCCGCTCCCCAGGCCTGCAGGAG TAAAATCAGGACCGGGTCGTGTCCGAGCCTACGGGCCCTGTCTCCGCTCCCCAGGCCTGCAGGAG T C MIR210HG Ensembl:ENSG00000247095 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:567535..567634 26863196 MeRIP-seq:(Medium) rs115334811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1462074,Human_RBP_ID_18159620,Human_RBP_ID_22034139,Human_RBP_ID_26891384 57701 RMVar_ID_57701 Human_SNP_ID_452961770 m1A Human chr11 - 568400 568400 568400 GGGCCGGGGGGCGAGAGGGTGCCAGCGGCCGCAGCTGAAGTTGGGCCGAGAGCCGGCGACGGCCC GGGCCGGGGGGCGAGAGGGTGCCAGCGGCCGCGGCTGAAGTTGGGCCGAGAGCCGGCGACGGCCC T C MIR210HG Ensembl:ENSG00000247095 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:567831..568435;chr11:567782..568432 26863196 MeRIP-seq:(Medium) rs887358839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807127,Human_RBP_ID_4183870,Human_RBP_ID_5167293,Human_RBP_ID_5313461,Human_RBP_ID_5551186,Human_RBP_ID_9413921,Human_RBP_ID_18159115,Human_RBP_ID_18416696,Human_RBP_ID_18973044,Human_RBP_ID_22471716,Human_RBP_ID_26767854 Human_Splice_Rec_1193745,Human_Splice_Rec_1193747,Human_Splice_Rec_1193749,Human_Splice_Rec_1193751,Human_Splice_Rec_1193753 57702 RMVar_ID_57702 Human_SNP_ID_452964153 m1A Human chr11 + 574783 574783 574783 CGCCGCTGGCCCTCGGTGAGTCGCAGTGGCCCACCCTGCTGCACCCAGGCTCCCTCCCCCGCCTG CGCCGCTGGCCCTCGGTGAGTCGCAGTGGCCCCCCCTGCTGCACCCAGGCTCCCTCCCCCGCCTG A C lnc-PHRF1-1 RNACentral:URS00008BB238 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:574739..574870 26863196 MeRIP-seq:(Medium) rs907986005 Functional Loss SNV dbSNP153 33..33 33 - - - 57703 RMVar_ID_57703 Human_SNP_ID_452964306 m1A Human chr11 - 575299 575290 575299 GCTTGAGAACCGACGCCGGAGAGACGGGGAAGACGGGGGAGGCCTGAGCGCGGGCTGGCATGGCT GCTTGAGAACCGACGCCGGAGAGACGGGGAAG_________GCCTGAGCGCGGGCTGGCATGGCT CCTCCCCCGT C LOC143666,LOC143666:2,LOC143666:3,LOC143666:4,LOC143666:5 RNACentral:URS000075C0FE,RNACentral:URS00008C1AF6,RNACentral:URS0000D59EC9,RNACentral:URS00009B1B20,RNACentral:URS0000D5BC6B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:575003..575485 26863196 MeRIP-seq:(Medium) rs1319227249 Functional Loss DEL dbSNP153 33..41 33 - - - 57704 RMVar_ID_57704 Human_SNP_ID_452964322 m1A Human chr11 - 575324 575324 575324 GGAGAAATGAGGCGGGGAAGGACGAGCTTGAGAACCGACGCCGGAGAGACGGGGAAGACGGGGGA GGAGAAATGAGGCGGGGAAGGACGAGCTTGAGCACCGACGCCGGAGAGACGGGGAAGACGGGGGA T G LOC143666,LOC143666:2,LOC143666:3,LOC143666:4,LOC143666:5 RNACentral:URS000075C0FE,RNACentral:URS00008C1AF6,RNACentral:URS0000D59EC9,RNACentral:URS00009B1B20,RNACentral:URS0000D5BC6B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:575273..575413 26863196 MeRIP-seq:(Medium) rs1290372720 Functional Loss SNV dbSNP153 33..33 33 - - - 57705 RMVar_ID_57705 Human_SNP_ID_452964365 m1A Human chr11 + 575435 575435 575435 GGAGCCGGCACTTCCCACACCTGCGCAGACCCACCCGGGCCCCAGCCCAGGCAGCCCCTGCACGG GGAGCCGGCACTTCCCACACCTGCGCAGACCCGCCCGGGCCCCAGCCCAGGCAGCCCCTGCACGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:575386..575505 32194978 MeRIP-seq:(Medium) rs995918276 Functional Loss SNV dbSNP153 33..33 33 - - - 57706 RMVar_ID_57706 Human_SNP_ID_452964835 m1A Human chr11 + 576505 576505 576505 CTTCCGGGTCGAAGAGCGCACGGCGGCGGCAGAGGCGGCGGCGGCCGGGCCTAGGAGCGACTCTC CTTCCGGGTCGAAGAGCGCACGGCGGCGGCAGGGGCGGCGGCGGCCGGGCCTAGGAGCGACTCTC A G PHRF1 Ensembl:ENSG00000070047 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:576472..576614 26863196 MeRIP-seq:(Medium) rs1177230225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416697 Human_Splice_Rec_1193755,Human_Splice_Rec_1193789,Human_Splice_Rec_1193823,Human_Splice_Rec_1193857,Human_Splice_Rec_1193891 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57707 RMVar_ID_57707 Human_SNP_ID_452964847 m1A Human chr11 - 576524 576524 576524 TCGCCGCCGCTGCACGACCGAGAGTCGCTCCTAGGCCCGGCCGCCGCCGCCTCTGCCGCCGCCGT TCGCCGCCGCTGCACGACCGAGAGTCGCTCCTCGGCCCGGCCGCCGCCGCCTCTGCCGCCGCCGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:576476..587265 26863196 MeRIP-seq:(Medium) rs1023512955 Functional Loss SNV dbSNP153 33..33 33 - - - 57708 RMVar_ID_57708 Human_SNP_ID_452972635 m1A Human chr11 + 597484 597484 597484 CCACCAGCAGGCTTCGGCCTCGAGCAGGTAGGACCCGGGCGATAGCCAGGACACGGCAGAGTGAG CCACCAGCAGGCTTCGGCCTCGAGCAGGTAGGTCCCGGGCGATAGCCAGGACACGGCAGAGTGAG A T PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:597434..597602 26863196 MeRIP-seq:(Medium) rs1373094930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8770101,Human_RBP_ID_11649218,Human_RBP_ID_17797556,Human_RBP_ID_27412470 Human_Splice_Rec_1193768,Human_Splice_Rec_1193769,Human_Splice_Rec_1193802,Human_Splice_Rec_1193803,Human_Splice_Rec_1193836,Human_Splice_Rec_1193837,Human_Splice_Rec_1193870,Human_Splice_Rec_1193871,Human_Splice_Rec_1193904,Human_Splice_Rec_1193905 RMVar_hsa_circ_18825,RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_68954,RMVar_hsa_circ_37675,RMVar_hsa_circ_47497,RMVar_hsa_circ_352573,RMVar_hsa_circ_377204,RMVar_hsa_circ_292143,RMVar_hsa_circ_147424,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425,RMVar_hsa_circ_27297,RMVar_hsa_circ_304603,RMVar_hsa_circ_330275,RMVar_hsa_circ_147427 57709 RMVar_ID_57709 Human_SNP_ID_452974099 m1A Human chr11 + 601626 601626 601626 GGAAGAAAGAAAACCCCGTCCGGACCATCCGCAAAAAGTAAGAGCTCAGCGACAAGATCTAAGAA GGAAGAAAGAAAACCCCGTCCGGACCATCCGCCAAAAGTAAGAGCTCAGCGACAAGATCTAAGAA A C PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:598444..601737 26863196 MeRIP-seq:(Medium) rs764215194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29424,Human_RBP_ID_866986,Human_RBP_ID_3940054,Human_RBP_ID_11649279,Human_RBP_ID_24542291 Human_Splice_Rec_1193772,Human_Splice_Rec_1193773,Human_Splice_Rec_1193806,Human_Splice_Rec_1193807,Human_Splice_Rec_1193840,Human_Splice_Rec_1193841,Human_Splice_Rec_1193874,Human_Splice_Rec_1193875,Human_Splice_Rec_1193908,Human_Splice_Rec_1193909,Human_Splice_Rec_1193925 Human_miRNA_ID_2005181 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_37675,RMVar_hsa_circ_292143,RMVar_hsa_circ_147424,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425,RMVar_hsa_circ_67990 57710 RMVar_ID_57710 Human_SNP_ID_452974100 m1A Human chr11 + 601627 601627 601627 GAAGAAAGAAAACCCCGTCCGGACCATCCGCAAAAAGTAAGAGCTCAGCGACAAGATCTAAGAAA GAAGAAAGAAAACCCCGTCCGGACCATCCGCAGAAAGTAAGAGCTCAGCGACAAGATCTAAGAAA A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:601537..601700 26863196 MeRIP-seq:(Medium) rs752114114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29424,Human_RBP_ID_866986,Human_RBP_ID_3940054,Human_RBP_ID_11649279,Human_RBP_ID_24542291 Human_Splice_Rec_1193772,Human_Splice_Rec_1193773,Human_Splice_Rec_1193806,Human_Splice_Rec_1193807,Human_Splice_Rec_1193840,Human_Splice_Rec_1193841,Human_Splice_Rec_1193874,Human_Splice_Rec_1193875,Human_Splice_Rec_1193908,Human_Splice_Rec_1193909,Human_Splice_Rec_1193925 Human_miRNA_ID_2005181 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_37675,RMVar_hsa_circ_292143,RMVar_hsa_circ_147424,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425,RMVar_hsa_circ_67990 57711 RMVar_ID_57711 Human_SNP_ID_452975228 m1A Human chr11 - 605099 605099 605099 TGGTGGCTTCACTCTGAATCCAGTAACAAAGAAAAAGATGAACAGAGAGACGGGGATGGCATCTA TGGTGGCTTCACTCTGAATCCAGTAACAAAGATAAAGATGAACAGAGAGACGGGGATGGCATCTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:605095..605178 26863196 MeRIP-seq:(Medium) rs1020840107 Functional Loss SNV dbSNP153 33..33 33 - - - 57712 RMVar_ID_57712 Human_SNP_ID_452975275 m1A Human chr11 - 605175 605175 605175 GGCTTCAACACTGACGGGATGCAGCTGCTGTGAACAGGCCTGCGCAGGCCCAGCGTCCGCGCGAT GGCTTCAACACTGACGGGATGCAGCTGCTGTGTACAGGCCTGCGCAGGCCCAGCGTCCGCGCGAT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:601664..605231 32194978 MeRIP-seq:(Medium) rs191003484 Functional Loss SNV dbSNP153 33..33 33 - - - 57713 RMVar_ID_57713 Human_SNP_ID_452975439 m1A Human chr11 - 605638 605638 605638 GACCGGGACAGAGCCCGTCTCTTGGCACTCAGAGGGGAAAGAGGGTTTGCAGAAAGCTCTTCACT GACCGGGACAGAGCCCGTCTCTTGGCACTCAGGGGGGAAAGAGGGTTTGCAGAAAGCTCTTCACT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:605634..606551 32194978 MeRIP-seq:(Medium) rs376870140 Functional Loss SNV dbSNP153 33..33 33 - - - 57714 RMVar_ID_57714 Human_SNP_ID_452976037 m1A Human chr11 - 607221 607221 607221 AGGCGCCCCCGCGGTGCGGGCGGGGGTGCGGGACCTGCCTTGACAGCTGAGCCCTGTGCTCTGTG AGGCGCCCCCGCGGTGCGGGCGGGGGTGCGGGCCCTGCCTTGACAGCTGAGCCCTGTGCTCTGTG T G lnc-IRF7-1 RNACentral:URS0000D5ADFC lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:607170..607370 32194978 MeRIP-seq:(Medium) rs761047986 Functional Loss SNV dbSNP153 33..33 33 - - - 57715 RMVar_ID_57715 Human_SNP_ID_452976392 m1A Human chr11 - 607903 607903 607903 TCCGCAGCTGCTTCGTCTTCTTGATGGAGAAGAGGGGTGAGGGGTTCTCCTTCCTCTGCTCCTTA TCCGCAGCTGCTTCGTCTTCTTGATGGAGAAGGGGGGTGAGGGGTTCTCCTTCCTCTGCTCCTTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:607568..607967 32194978 MeRIP-seq:(Medium) rs999084333 Functional Loss SNV dbSNP153 33..33 33 - - - 57716 RMVar_ID_57716 Human_SNP_ID_452976405 m1A Human chr11 + 607935 607935 607935 TCTTCTCCATCAAGAAGACGAAGCAGCTGCGGAGCGAGGTCTACGACCCATCCGACCCCACCGGC TCTTCTCCATCAAGAAGACGAAGCAGCTGCGGGGCGAGGTCTACGACCCATCCGACCCCACCGGC A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:607886..608120 26863196 MeRIP-seq:(Medium) rs770644662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57717 RMVar_ID_57717 Human_SNP_ID_452976416 m1A Human chr11 + 607952 607952 607952 ACGAAGCAGCTGCGGAGCGAGGTCTACGACCCATCCGACCCCACCGGCTCCGACTCCAGCGCCCC ACGAAGCAGCTGCGGAGCGAGGTCTACGACCCTTCCGACCCCACCGGCTCCGACTCCAGCGCCCC A T PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:607903..608129 26863196 MeRIP-seq:(Medium) rs368400216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57718 RMVar_ID_57718 Human_SNP_ID_452976820 m1A Human chr11 + 608604 608604 608604 AGGAGCGCCCCAGGAGGCAGCGGTCCAAGGCCAAGAGCCGGCGGTCCTCCAGTGACCGCTCCAGC AGGAGCGCCCCAGGAGGCAGCGGTCCAAGGCCGAGAGCCGGCGGTCCTCCAGTGACCGCTCCAGC A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:608553..609000 26863196 MeRIP-seq:(Medium) rs775564327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57719 RMVar_ID_57719 Human_SNP_ID_452976949 m1A Human chr11 - 608802 608802 608802 GGTGGGGGAGCACTCCCTTCCCCGAGGTCTGGACGCTGATCTCCTTTTCTTCTTCTTCCTACTCT GGTGGGGGAGCACTCCCTTCCCCGAGGTCTGGTCGCTGATCTCCTTTTCTTCTTCTTCCTACTCT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:608701..608930 26863196 MeRIP-seq:(Medium) rs370766202 Functional Loss SNV dbSNP153 33..33 33 - - - 57720 RMVar_ID_57720 Human_SNP_ID_452976950 m1A Human chr11 - 608802 608802 608802 GGTGGGGGAGCACTCCCTTCCCCGAGGTCTGGACGCTGATCTCCTTTTCTTCTTCTTCCTACTCT GGTGGGGGAGCACTCCCTTCCCCGAGGTCTGGGCGCTGATCTCCTTTTCTTCTTCTTCCTACTCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:608701..608930 26863196 MeRIP-seq:(Medium) rs370766202 Functional Loss SNV dbSNP153 33..33 33 - - - 57721 RMVar_ID_57721 Human_SNP_ID_452976999 m1A Human chr11 + 608894 608894 608894 AAGCATCAGCGGGAACGCAGCCACGAGCGGCCAGACAGGAAGGAGAGTGTGGCGTGGCCCCGAGA AAGCATCAGCGGGAACGCAGCCACGAGCGGCCGGACAGGAAGGAGAGTGTGGCGTGGCCCCGAGA A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:608481..609011 26863196 MeRIP-seq:(Medium) rs1289520096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24542705 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57722 RMVar_ID_57722 Human_SNP_ID_452977850 m1A Human chr11 + 610300 610300 610300 TCAGGCAGGTGTTCTCCGAGCTGCCCTTTCCCAGTCACGTGCTTCCGGAACCCGGGTTCCCAGAC TCAGGCAGGTGTTCTCCGAGCTGCCCTTTCCCGGTCACGTGCTTCCGGAACCCGGGTTCCCAGAC A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:610250..610347 26863196 MeRIP-seq:(Medium) rs201244128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18609252,Human_RBP_ID_22790725,Human_RBP_ID_26892026 Human_Splice_Rec_1193783,Human_Splice_Rec_1193817,Human_Splice_Rec_1193851,Human_Splice_Rec_1193885,Human_Splice_Rec_1193919 Human_miRNA_ID_2037255,Human_miRNA_ID_2347958 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 57723 RMVar_ID_57723 Human_SNP_ID_452978508 m1A Human chr11 - 611716 611716 611716 CCTCCCCGGCCTCTGGTTTCTTGTGCCTGCGCATGTGCCTGTACTTGTCCACGTACGCCTTCACC CCTCCCCGGCCTCTGGTTTCTTGTGCCTGCGCGTGTGCCTGTACTTGTCCACGTACGCCTTCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:611626..611971 26863196 MeRIP-seq:(Medium) rs750587636 Functional Loss SNV dbSNP153 33..33 33 - - - 57724 RMVar_ID_57724 Human_SNP_ID_452978509 m1A Human chr11 - 611716 611716 611716 CCTCCCCGGCCTCTGGTTTCTTGTGCCTGCGCATGTGCCTGTACTTGTCCACGTACGCCTTCACC CCTCCCCGGCCTCTGGTTTCTTGTGCCTGCGCCTGTGCCTGTACTTGTCCACGTACGCCTTCACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:611626..611971 26863196 MeRIP-seq:(Medium) rs750587636 Functional Loss SNV dbSNP153 33..33 33 - - - 57725 RMVar_ID_57725 Human_SNP_ID_452980006 m1A Human chr11 + 614302 614302 614302 GGTCTGCCAGGCAGCTCTGTTGCACTGCCTGGAGCAGGAGGTCCCCCTTGTCACCAGCTGGGGCA GGTCTGCCAGGCAGCTCTGTTGCACTGCCTGGGGCAGGAGGTCCCCCTTGTCACCAGCTGGGGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:614178..614328 32194978 MeRIP-seq:(Medium) rs1337321351 Functional Loss SNV dbSNP153 33..33 33 - - - 57726 RMVar_ID_57726 Human_SNP_ID_452980563 m1A Human chr11 - 615213 615213 615213 TGCTGTTCGGAGAGTGGCTCCTTGGAGAGATCAGCAGCGGCTGCTATGAGGGGCTGCAGTGGCTG TGCTGTTCGGAGAGTGGCTCCTTGGAGAGATCGGCAGCGGCTGCTATGAGGGGCTGCAGTGGCTG T C IRF7 Ensembl:ENSG00000185507 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:615176..615370 26863196 MeRIP-seq:(Medium) rs1420766879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1193966,Human_Splice_Rec_1193984,Human_Splice_Rec_1194004,Human_Splice_Rec_1194032,Human_Splice_Rec_1194070,Human_Splice_Rec_1194098,Human_Splice_Rec_1194106,Human_Splice_Rec_1194120 57727 RMVar_ID_57727 Human_SNP_ID_452980596 m1A Human chr11 + 615280 615278 615280 CGTGGGGCTGCCCTGCGGGTGCCCGGCCGCGGAGAGTCAGGGCCGGCTGCAGGGCGCTCGGGGAC CGTGGGGCTGCCCTGCGGGTGCCCGGCCGCG__GAGTCAGGGCCGGCTGCAGGGCGCTCGGGGAC GGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:615229..615368 26863196 MeRIP-seq:(Medium) rs772080975 Functional Loss DEL dbSNP153 32..33 33 - - - 57728 RMVar_ID_57728 Human_SNP_ID_452980699 m1A Human chr11 - 615484 615475 615485 GGTGGCTACAAGCCCTCAGTCCACACCTGTGGACACCTGTGACACCTGGCCACACGACCTGTGGC GGTGGCTACAAGCCCTCAGTCCACACCTGTG__________ACACCTGGCCACACGACCTGTGGC TCACAGGTGTC T IRF7 Ensembl:ENSG00000185507 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:615477..615639 26863196 MeRIP-seq:(Medium) rs958732146 Functional Loss DEL dbSNP153 32..41 33 - - - 57729 RMVar_ID_57729 Human_SNP_ID_452983815 m1A Human chr11 - 621632 621632 621632 GGACACGAAAGTGAACTCCACCGTCATCCCCGAGACGCAACTGCAGGCTGAGGACCGCGACAAGG GGACACGAAAGTGAACTCCACCGTCATCCCCGGGACGCAACTGCAGGCTGAGGACCGCGACAAGG T C CDHR5 Ensembl:ENSG00000099834 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:621583..621739 26863196 MeRIP-seq:(Medium) rs963294461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1194128,Human_Splice_Rec_1194129,Human_Splice_Rec_1194156,Human_Splice_Rec_1194157,Human_Splice_Rec_1194184,Human_Splice_Rec_1194185,Human_Splice_Rec_1194212,Human_Splice_Rec_1194213,Human_Splice_Rec_1194240,Human_Splice_Rec_1194241,Human_Splice_Rec_1194266,Human_Splice_Rec_1194267,Human_Splice_Rec_1194290,Human_Splice_Rec_1194291,Human_Splice_Rec_1194302,Human_Splice_Rec_1194303,Human_Splice_Rec_1194312,Human_Splice_Rec_1194313 57730 RMVar_ID_57730 Human_SNP_ID_452984672 m1A Human chr11 + 624074 624074 624074 TCCACAGCTCAGGGCAGAGTCTGGACTGGAGGAAATGTGGGCATCACCCTCGGGGGGGTGGAATT TCCACAGCTCAGGGCAGAGTCTGGACTGGAGGTAATGTGGGCATCACCCTCGGGGGGGTGGAATT A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:623946..624075 26863196 MeRIP-seq:(Medium) rs1272535819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657360 57731 RMVar_ID_57731 Human_SNP_ID_452985742 m1A Human chr11 + 626573 626573 626573 AGCACGTGAGGGTCTGAGGGCTGGGGCTGGAGACCCCGGCCCCGCTGCTGGAATTGGGCCTCCAG AGCACGTGAGGGTCTGAGGGCTGGGGCTGGAGGCCCCGGCCCCGCTGCTGGAATTGGGCCTCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:626568..626677 26863196 MeRIP-seq:(Medium) rs748314311 Functional Loss SNV dbSNP153 33..33 33 - - - 57732 RMVar_ID_57732 Human_SNP_ID_452985812 m1A Human chr11 - 626719 626716 626720 TCAGCGCGGGTCTGCTCTGCCCGTCAGGGTCCAACATGCCCATCCTGCAGGCCTGGTGAGCACCC TCAGCGCGGGTCTGCTCTGCCCGTCAGGGTC____ATGCCCATCCTGCAGGCCTGGTGAGCACCC TGTTG T SCT Ensembl:ENSG00000070031 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:626717..626878 26863196 MeRIP-seq:(Medium) rs1411727419 Functional Loss DEL dbSNP153 32..35 33 - - - Human_Splice_Rec_1194322,Human_Splice_Rec_1194323 57733 RMVar_ID_57733 Human_SNP_ID_452986979 m1A Human chr11 - 628873 628873 628873 GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCAGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCTGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:628823..629118 26863196 MeRIP-seq:(Medium) rs924513523 Functional Loss SNV dbSNP153 33..33 33 - - - 57734 RMVar_ID_57734 Human_SNP_ID_452986980 m1A Human chr11 - 628873 628873 628873 GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCAGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCGGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:628823..629118 26863196 MeRIP-seq:(Medium) rs924513523 Functional Loss SNV dbSNP153 33..33 33 - - - 57735 RMVar_ID_57735 Human_SNP_ID_452986981 m1A Human chr11 - 628873 628873 628873 GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCAGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT GAAAGAAAAGCAAGCAAGCCAGCAAGCCAGCCCGCCAGCCAGCCCCACATTGCTGGCGGGGCTGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:628823..629118 26863196 MeRIP-seq:(Medium) rs924513523 Functional Loss SNV dbSNP153 33..33 33 - - - 57736 RMVar_ID_57736 Human_SNP_ID_452989431 m1A Human chr11 + 635561 635561 635561 AAGAGTGAAACTCCATCTCAAAAAAAAAAAAAAAAAAAAAACAAATTGGGGTTGTCTGTCTTTTC AAGAGTGAAACTCCATCTCAAAAAAAAAAAAACAAAAAAAACAAATTGGGGTTGTCTGTCTTTTC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:635550..635637 26863410 MeRIP-seq:(Medium) rs945057619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3377408 57737 RMVar_ID_57737 Human_SNP_ID_452989995 m1A Human chr11 - 636784 636746 636784 CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCACCCTCCACGCCCGCTCCCCCTGCCCCCGACTC CTCCCCCGCGGACTCGCCTCGACCTCGTGCGC_________________________________ GGCGCGGAGTCGGGGGCAGGGGGAGCGGGCGTGGAGGGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:636735..637076 26863196 MeRIP-seq:(Medium) rs1284116530 Functional Loss DEL dbSNP153 33..65 33 - - - 57738 RMVar_ID_57738 Human_SNP_ID_452990002 m1A Human chr11 - 636784 636762 636784 CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCACCCTCCACGCCCGCTCCCCCTGCCCCCGACTC CTCCCCCGCGGACTCGCCTCGACCTCGTGCGC______________________GCCCCCGACTC CAGGGGGAGCGGGCGTGGAGGGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:636735..637076 26863196 MeRIP-seq:(Medium) rs1313714971 Functional Loss DEL dbSNP153 33..54 33 - - - 57739 RMVar_ID_57739 Human_SNP_ID_452990020 m1A Human chr11 - 636784 636782 636784 CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCACCCTCCACGCCCGCTCCCCCTGCCCCCGACTC CTCCCCCGCGGACTCGCCTCGACCTCGTGCGC__CCTCCACGCCCGCTCCCCCTGCCCCCGACTC GGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:636735..637076 26863196 MeRIP-seq:(Medium) rs1384052241 Functional Loss DEL dbSNP153 33..34 33 - - - 57740 RMVar_ID_57740 Human_SNP_ID_452990023 m1A Human chr11 - 636784 636784 636784 CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCACCCTCCACGCCCGCTCCCCCTGCCCCCGACTC CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCGCCCTCCACGCCCGCTCCCCCTGCCCCCGACTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:636735..637076 26863196 MeRIP-seq:(Medium) rs1800955 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6797,GWAS_ID_6798,GWAS_ID_6799,GWAS_ID_6800,GWAS_ID_6801,GWAS_ID_6802,GWAS_ID_6803,GWAS_ID_6804 57741 RMVar_ID_57741 Human_SNP_ID_452990024 m1A Human chr11 - 636784 636784 636784 CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCACCCTCCACGCCCGCTCCCCCTGCCCCCGACTC CTCCCCCGCGGACTCGCCTCGACCTCGTGCGCCCCCTCCACGCCCGCTCCCCCTGCCCCCGACTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:636735..637076 26863196 MeRIP-seq:(Medium) rs1800955 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6797,GWAS_ID_6798,GWAS_ID_6799,GWAS_ID_6800,GWAS_ID_6801,GWAS_ID_6802,GWAS_ID_6803,GWAS_ID_6804 57742 RMVar_ID_57742 Human_SNP_ID_452990043 m1A Human chr11 + 636815 636815 636815 GTGCGCACGAGGTCGAGGCGAGTCCGCGGGGGAGGCGGGCAGAGCCTGAGCTCAGGTCTTTCTGC GTGCGCACGAGGTCGAGGCGAGTCCGCGGGGGGGGCGGGCAGAGCCTGAGCTCAGGTCTTTCTGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:636806..636949 26863196 MeRIP-seq:(Medium) rs1285581917 Functional Loss SNV dbSNP153 33..33 33 - - - 57743 RMVar_ID_57743 Human_SNP_ID_452990375 m1A Human chr11 - 637397 637397 637397 ACGCCCCCCACCAGCGCCGCCGCGCCCTGCCCAGCCAGCCCCGCAGATGCCCCCGCAGATGCCCC ACGCCCCCCACCAGCGCCGCCGCGCCCTGCCCTGCCAGCCCCGCAGATGCCCCCGCAGATGCCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:637390..637588 26863196 MeRIP-seq:(Medium) rs1265014684 Functional Loss SNV dbSNP153 33..33 33 - - - 57744 RMVar_ID_57744 Human_SNP_ID_452991471 m1A Human chr11 + 639431 639431 639431 GGGAAACCTCAGGGCCTGTGGTGTCGCCGCGCAGGTCCAGGGTGGCGCGTGGCTGCTGAGCCCCC GGGAAACCTCAGGGCCTGTGGTGTCGCCGCGCCGGTCCAGGGTGGCGCGTGGCTGCTGAGCCCCC A C DRD4 Ensembl:ENSG00000069696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:639422..639548 26863196 MeRIP-seq:(Medium) rs1369849868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259561,Human_RBP_ID_3384618,Human_RBP_ID_5313936,Human_RBP_ID_8063033,Human_RBP_ID_8229021,Human_RBP_ID_8940599,Human_RBP_ID_9414730,Human_RBP_ID_17648499,Human_RBP_ID_18159131,Human_RBP_ID_18188415,Human_RBP_ID_18416701,Human_RBP_ID_18456233,Human_RBP_ID_18477341,Human_RBP_ID_22695478,Human_RBP_ID_22708645,Human_RBP_ID_24362880 57745 RMVar_ID_57745 Human_SNP_ID_452991968 m1A Human chr11 - 640065 640017 640065 GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGGACCCCGGGGAAGGCCGGGCGCGGGGGGCGCACA GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGG_________________________________ CCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:639885..640233;chr11:640028..640203 26863196 MeRIP-seq:(Medium) rs1429763859 Functional Loss DEL dbSNP153 33..65 33 - - - 57746 RMVar_ID_57746 Human_SNP_ID_452991971 m1A Human chr11 + 640031 640022 640032 GCCCCGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGG GCCCCGCCTCCCCCAGGACCCCTG__________TGTGCGCCCCCCGCGCCCGGCCTTCCCCGGG GCGGCCCCGAC G DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:640019..640257 26863196 MeRIP-seq:(Medium) rs776759649 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_26776022 57747 RMVar_ID_57747 Human_SNP_ID_452991985 m1A Human chr11 + 640031 640031 640031 GCCCCGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGG GCCCCGCCTCCCCCAGGACCCCTGCGGCCCCGCCTGTGCGCCCCCCGCGCCCGGCCTTCCCCGGG A C DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:640019..640257 26863196 MeRIP-seq:(Medium) rs1564913740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26776022 57748 RMVar_ID_57748 Human_SNP_ID_452992022 m1A Human chr11 - 640065 640065 640065 GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGGACCCCGGGGAAGGCCGGGCGCGGGGGGCGCACA GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGGGCCCCGGGGAAGGCCGGGCGCGGGGGGCGCACA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:639885..640233;chr11:640028..640203 26863196 MeRIP-seq:(Medium) rs1256049181 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57749 RMVar_ID_57749 Human_SNP_ID_452992023 m1A Human chr11 - 640065 640065 640065 GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGGACCCCGGGGAAGGCCGGGCGCGGGGGGCGCACA GGCGCGGCGGGCGCACAGTCGGGGCCGCAGGGCCCCCGGGGAAGGCCGGGCGCGGGGGGCGCACA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:639885..640233;chr11:640028..640203 26863196 MeRIP-seq:(Medium) rs1256049181 Functional Loss SNV dbSNP153 33..33 33 - - - 57750 RMVar_ID_57750 Human_SNP_ID_452992026 m1A Human chr11 + 640079 640070 640080 GCCCGGCCTTCCCCGGGGTCCCTGCGGCCCCGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGG GCCCGGCCTTCCCCGGGGTCCCTG__________TGTGCGCCCGCCGCGCCCAGCCTCCCCCAGG GCGGCCCCGAC G DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr11:639525..640268;chr11:640046..640256 26863196 MeRIP-seq:(Medium) rs762885973 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_3384621,Human_RBP_ID_8173867,Human_RBP_ID_26775518 57751 RMVar_ID_57751 Human_SNP_ID_452992080 m1A Human chr11 + 640109 640108 640109 CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCC_GGACCCCTGCGGCCCCGACTGTGCGCCCCCCG CA C DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:639978..640162 26863196 MeRIP-seq:(Medium) rs1344788742 Functional Loss DEL dbSNP153 33..33 33 - - - 57752 RMVar_ID_57752 Human_SNP_ID_452992082 m1A Human chr11 + 640109 640109 640109 CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCCGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG A C DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:639978..640162 26863196 MeRIP-seq:(Medium) rs769762387 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57753 RMVar_ID_57753 Human_SNP_ID_452992083 m1A Human chr11 + 640109 640109 640109 CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCGGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG A G DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:639978..640162 26863196 MeRIP-seq:(Medium) rs769762387 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57754 RMVar_ID_57754 Human_SNP_ID_452992136 m1A Human chr11 - 640151 640151 640151 GAGCACAGTTGGAGCCGCAGGGGTCCGGGGGGAGGCCGGGCGCGGGGGGCGCACAGTCGGGGCCG GAGCACAGTTGGAGCCGCAGGGGTCCGGGGGGGGGCCGGGCGCGGGGGGCGCACAGTCGGGGCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:639737..640627 26863196 MeRIP-seq:(Medium) rs1231044744 Functional Loss SNV dbSNP153 33..33 33 - - - 57755 RMVar_ID_57755 Human_SNP_ID_452992387 m1A Human chr11 + 640378 640378 640378 GGGGGTACGAGGCCGGCTGGGCGGGGGGCGCTAACGCGGCTCTCGGCGCCCCCAGGGGCCTTCCT GGGGGTACGAGGCCGGCTGGGCGGGGGGCGCTGACGCGGCTCTCGGCGCCCCCAGGGGCCTTCCT A G DRD4 Ensembl:ENSG00000069696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:640370..640629 26863196 MeRIP-seq:(Medium) rs200635197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259562,Human_RBP_ID_3383786,Human_RBP_ID_5235159,Human_RBP_ID_5313937,Human_RBP_ID_5343208,Human_RBP_ID_5643974,Human_RBP_ID_8173868,Human_RBP_ID_8229150,Human_RBP_ID_8725252,Human_RBP_ID_18159133,Human_RBP_ID_22568322,Human_RBP_ID_22642673,Human_RBP_ID_22708646,Human_RBP_ID_24362962,Human_RBP_ID_24405165,Human_RBP_ID_26776024 57756 RMVar_ID_57756 Human_SNP_ID_452993519 m1A Human chr11 + 642800 642775 642801 GGTCACAGGAAGGGCCAGGCGGGGTGAGGGTCACAGGAAGGGCCAGGCGGGCTGAGGGTCACAGG GGTCACAG__________________________AGGAAGGGCCAGGCGGGCTGAGGGTCACAGG GGAAGGGCCAGGCGGGGTGAGGGTCAC G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:642710..642850 26863196 MeRIP-seq:(Medium) rs1237211089 Functional Loss DEL dbSNP153 9..34 33 - - - 57757 RMVar_ID_57757 Human_SNP_ID_452999577 m1A Human chr11 - 660409 660409 660409 AAAGCACAGAGGTGGCTTTGCAGTCCCACTTCAGGGGGACCCTGCCTGACCTGGGATGAGGTGTG AAAGCACAGAGGTGGCTTTGCAGTCCCACTTCGGGGGGACCCTGCCTGACCTGGGATGAGGTGTG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:660407..660582 26863196 MeRIP-seq:(Medium) rs370638923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9414405 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 57758 RMVar_ID_57758 Human_SNP_ID_452999578 m1A Human chr11 - 660409 660409 660409 AAAGCACAGAGGTGGCTTTGCAGTCCCACTTCAGGGGGACCCTGCCTGACCTGGGATGAGGTGTG AAAGCACAGAGGTGGCTTTGCAGTCCCACTTCCGGGGGACCCTGCCTGACCTGGGATGAGGTGTG T G DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:660407..660582 26863196 MeRIP-seq:(Medium) rs370638923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9414405 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 57759 RMVar_ID_57759 Human_SNP_ID_453005408 m1A Human chr11 + 679802 679802 679802 GGTCAGTGCCCCCGAGGTCGTGATCTGTCCCGAGGGGGTCACGGTGACTGGAAAGGCAGAAGCAC GGTCAGTGCCCCCGAGGTCGTGATCTGTCCCGGGGGGGTCACGGTGACTGGAAAGGCAGAAGCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:679754..679851 26863196 MeRIP-seq:(Medium) rs1449039506 Functional Loss SNV dbSNP153 33..33 33 - - - 57760 RMVar_ID_57760 Human_SNP_ID_453005415 m1A Human chr11 - 679818 679818 679818 CCTGGCCGCGTGAAATGTGCTTCTGCCTTTCCAGTCACCGTGACCCCCTCGGGACAGATCACGAC CCTGGCCGCGTGAAATGTGCTTCTGCCTTTCCGGTCACCGTGACCCCCTCGGGACAGATCACGAC T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:679778..680039 32194978 MeRIP-seq:(Medium) rs1172997135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402289,Human_RBP_ID_24899808 RMVar_hsa_circ_23519,RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_311192,RMVar_hsa_circ_147431,RMVar_hsa_circ_329909,RMVar_hsa_circ_294046,RMVar_hsa_circ_375113,RMVar_hsa_circ_38833,RMVar_hsa_circ_36902,RMVar_hsa_circ_147432,RMVar_hsa_circ_147433,RMVar_hsa_circ_285909,RMVar_hsa_circ_83217,RMVar_hsa_circ_147436,RMVar_hsa_circ_147437 57761 RMVar_ID_57761 Human_SNP_ID_453005844 m1A Human chr11 - 681013 681011 681014 GGAGAATGAACTGCCCACAACTCCCGTGAAGAAGGACTCCCCCAAGAACATCACATTGCTTCCAG GGAGAATGAACTGCCCACAACTCCCGTGAAG___GACTCCCCCAAGAACATCACATTGCTTCCAG CCTT C DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:680926..681050 26863196 MeRIP-seq:(Medium) rs1356093579 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3378877,Human_RBP_ID_11689858,Human_RBP_ID_18611913 Human_Splice_Rec_1194340,Human_Splice_Rec_1194341,Human_Splice_Rec_1194362,Human_Splice_Rec_1194363,Human_Splice_Rec_1194375,Human_Splice_Rec_1194386,Human_Splice_Rec_1194387 RMVar_hsa_circ_23519,RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_311192,RMVar_hsa_circ_147431,RMVar_hsa_circ_329909,RMVar_hsa_circ_294046,RMVar_hsa_circ_375113,RMVar_hsa_circ_38833,RMVar_hsa_circ_36902,RMVar_hsa_circ_147432,RMVar_hsa_circ_147433,RMVar_hsa_circ_285909,RMVar_hsa_circ_83217,RMVar_hsa_circ_31293,RMVar_hsa_circ_81212,RMVar_hsa_circ_147436,RMVar_hsa_circ_147437,RMVar_hsa_circ_362118,RMVar_hsa_circ_64112,RMVar_hsa_circ_147438 57762 RMVar_ID_57762 Human_SNP_ID_453007059 m1A Human chr11 - 684962 684962 684962 CTAATGCATGGTGGTTCTTTTCACATCTCAGGATGGGATCTTAAACCCTCACGCTGCCTCTTGCA CTAATGCATGGTGGTTCTTTTCACATCTCAGGTTGGGATCTTAAACCCTCACGCTGCCTCTTGCA T A DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:684932..686918 32194978 MeRIP-seq:(Medium) rs1421361308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22491715,Human_RBP_ID_26319458 Human_Splice_Rec_1194338,Human_Splice_Rec_1194339,Human_Splice_Rec_1194360,Human_Splice_Rec_1194361,Human_Splice_Rec_1194385 RMVar_hsa_circ_23519,RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_311192,RMVar_hsa_circ_147431,RMVar_hsa_circ_329909,RMVar_hsa_circ_375113,RMVar_hsa_circ_38833,RMVar_hsa_circ_36902,RMVar_hsa_circ_147432,RMVar_hsa_circ_83217,RMVar_hsa_circ_31293,RMVar_hsa_circ_147437,RMVar_hsa_circ_362118,RMVar_hsa_circ_64112,RMVar_hsa_circ_347691 57763 RMVar_ID_57763 Human_SNP_ID_453010073 m1A Human chr11 + 694301 694301 694301 TAGGCAGGTCACCAGGGGCAGGTGTGCGGGGCAGGTGTTTGGGGTAGGTGGGGCAGGCTGGTCAC TAGGCAGGTCACCAGGGGCAGGTGTGCGGGGCCGGTGTTTGGGGTAGGTGGGGCAGGCTGGTCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:694298..694379 26863196 MeRIP-seq:(Medium) rs1338093354 Functional Loss SNV dbSNP153 33..33 33 - - - 57764 RMVar_ID_57764 Human_SNP_ID_453010074 m1A Human chr11 + 694301 694301 694301 TAGGCAGGTCACCAGGGGCAGGTGTGCGGGGCAGGTGTTTGGGGTAGGTGGGGCAGGCTGGTCAC TAGGCAGGTCACCAGGGGCAGGTGTGCGGGGCGGGTGTTTGGGGTAGGTGGGGCAGGCTGGTCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:694298..694379 26863196 MeRIP-seq:(Medium) rs1338093354 Functional Loss SNV dbSNP153 33..33 33 - - - 57765 RMVar_ID_57765 Human_SNP_ID_453010342 m1A Human chr11 - 694899 694881 694899 GCCGGTGCTGAGCAGGGACGAGGACTCGGAGGAGGACGCAGACTCGGAGGCGGAGCGGGAGACGC GCCGGTGCTGAGCAGGGACGAGGACTCGGAGG__________________CGGAGCGGGAGACGC GCCTCCGAGTCTGCGTCCT G DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:694826..695050 26863196 MeRIP-seq:(Medium) rs1256713448 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_2818,Human_RBP_ID_227170,Human_RBP_ID_402637,Human_RBP_ID_3940066,Human_RBP_ID_4183872,Human_RBP_ID_5554439,Human_RBP_ID_6090644,Human_RBP_ID_9321177,Human_RBP_ID_11697414 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57766 RMVar_ID_57766 Human_SNP_ID_453010350 m1A Human chr11 - 694899 694899 694899 GCCGGTGCTGAGCAGGGACGAGGACTCGGAGGAGGACGCAGACTCGGAGGCGGAGCGGGAGACGC GCCGGTGCTGAGCAGGGACGAGGACTCGGAGGGGGACGCAGACTCGGAGGCGGAGCGGGAGACGC T C DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:694826..695050 26863196 MeRIP-seq:(Medium) rs889691540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2818,Human_RBP_ID_227170,Human_RBP_ID_402637,Human_RBP_ID_3940066,Human_RBP_ID_4183872,Human_RBP_ID_5554439,Human_RBP_ID_6090644,Human_RBP_ID_9321177,Human_RBP_ID_11697414 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57767 RMVar_ID_57767 Human_SNP_ID_453010362 m1A Human chr11 - 694914 694914 694914 AGGCGAGGCGGAGGAGCCGGTGCTGAGCAGGGACGAGGACTCGGAGGAGGACGCAGACTCGGAGG AGGCGAGGCGGAGGAGCCGGTGCTGAGCAGGGGCGAGGACTCGGAGGAGGACGCAGACTCGGAGG T C DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:694673..695185 26863196 MeRIP-seq:(Medium) rs1403325942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2818,Human_RBP_ID_227170,Human_RBP_ID_402637,Human_RBP_ID_4183872,Human_RBP_ID_6090644,Human_RBP_ID_9321177,Human_RBP_ID_11697414 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57768 RMVar_ID_57768 Human_SNP_ID_453010368 m1A Human chr11 + 694923 694923 694923 CTGCGTCCTCCTCCGAGTCCTCGTCCCTGCTCAGCACCGGCTCCTCCGCCTCGCCTCCTGCCGCG CTGCGTCCTCCTCCGAGTCCTCGTCCCTGCTCCGCACCGGCTCCTCCGCCTCGCCTCCTGCCGCG A C EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:694874..694987 26863196 MeRIP-seq:(Medium) rs1344300012 Functional Loss SNV dbSNP153 33..33 33 - - - 57769 RMVar_ID_57769 Human_SNP_ID_453010387 m1A Human chr11 - 694946 694946 694946 GCTGTGGCGGCGGCGGCCGCGGCCGCGGCAGGAGGCGAGGCGGAGGAGCCGGTGCTGAGCAGGGA GCTGTGGCGGCGGCGGCCGCGGCCGCGGCAGGGGGCGAGGCGGAGGAGCCGGTGCTGAGCAGGGA T C DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr11:694801..695050;chr11:694909..694999 26863410 MeRIP-seq:(Medium) rs1487162428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4176550,Human_RBP_ID_5313468,Human_RBP_ID_26776028 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57770 RMVar_ID_57770 Human_SNP_ID_453010407 m1A Human chr11 + 694992 694956 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT _________________________________CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCCGCGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs770980414 Functional Loss DEL dbSNP153 1..33 33 - - - 57771 RMVar_ID_57771 Human_SNP_ID_453010413 m1A Human chr11 + 694992 694959 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT _________________________________CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs1267034467 Functional Loss DEL dbSNP153 1..33 33 - - - 57772 RMVar_ID_57772 Human_SNP_ID_453010422 m1A Human chr11 + 694992 694962 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGG______________________________CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCCGCCGCCGCCACAGCGGCCGCGGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs748949371 Functional Loss DEL dbSNP153 4..33 33 - - - 57773 RMVar_ID_57773 Human_SNP_ID_453010425 m1A Human chr11 + 694992 694965 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGGCCG___________________________CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCCGCCGCCACAGCGGCCGCGGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs768085739 Functional Loss DEL dbSNP153,HGVD 7..33 33 - - - 57774 RMVar_ID_57774 Human_SNP_ID_453010428 m1A Human chr11 + 694974 694965 694974 CGCCTCCTGCCGCGGCCGCGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCA CGCCTCCTGCCGCGGCCGCGGCCG_________CAGCGGCCGCGGCCGCCACCGCCGCCGCCTCA GCCGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:694755..695025 26863410 MeRIP-seq:(Medium) rs1564956957 Functional Loss DEL dbSNP153 25..33 33 - - - 57775 RMVar_ID_57775 Human_SNP_ID_453010431 m1A Human chr11 + 694992 694968 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGGCCGCCG________________________CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCCGCCACAGCGGCCGCGGCCGCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs773843056 Functional Loss DEL dbSNP153 10..33 33 - - - 57776 RMVar_ID_57776 Human_SNP_ID_453010442 m1A Human chr11 + 694974 694974 694974 CGCCTCCTGCCGCGGCCGCGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCA CGCCTCCTGCCGCGGCCGCGGCCGCCGCCGCCTCAGCGGCCGCGGCCGCCACCGCCGCCGCCTCA A T EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:694755..695025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 57777 RMVar_ID_57777 Human_SNP_ID_453010464 m1A Human chr11 + 694992 694989 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGGCCGCCGCCGCCACAGCGGCCGCGGCCG___CCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT GCCA G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs1445772540 Functional Loss DEL dbSNP153 31..33 33 - - - 57778 RMVar_ID_57778 Human_SNP_ID_453010466 m1A Human chr11 + 694992 694992 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCGCCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs767318857 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57779 RMVar_ID_57779 Human_SNP_ID_453010478 m1A Human chr11 - 695004 695004 695004 GGACTCGGCGGCAAAGCAGCTGGGCCTGGCTGAGGCGGCGGCGGTGGCGGCCGCGGCCGCTGTGG GGACTCGGCGGCAAAGCAGCTGGGCCTGGCTGTGGCGGCGGCGGTGGCGGCCGCGGCCGCTGTGG T A DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:694876..695085 26863196 MeRIP-seq:(Medium) rs1481751613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227171,Human_RBP_ID_4184551,Human_RBP_ID_5313468,Human_RBP_ID_26776028 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57780 RMVar_ID_57780 Human_SNP_ID_453010479 m1A Human chr11 - 695004 695004 695004 GGACTCGGCGGCAAAGCAGCTGGGCCTGGCTGAGGCGGCGGCGGTGGCGGCCGCGGCCGCTGTGG GGACTCGGCGGCAAAGCAGCTGGGCCTGGCTGGGGCGGCGGCGGTGGCGGCCGCGGCCGCTGTGG T C DEAF1 Ensembl:ENSG00000177030 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:694876..695085 26863196 MeRIP-seq:(Medium) rs1481751613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227171,Human_RBP_ID_4184551,Human_RBP_ID_5313468,Human_RBP_ID_26776028 RMVar_hsa_circ_147439,RMVar_hsa_circ_86654 57781 RMVar_ID_57781 Human_SNP_ID_453010480 m1A Human chr11 + 695010 695008 695010 CGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTTGCCGCCGAGTCCGAGTCC CGGCCGCGGCCGCCACCGCCGCCGCCTCAGC__GGCCCAGCTGCTTTGCCGCCGAGTCCGAGTCC CCA C EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:694891..695134 26863196 MeRIP-seq:(Medium) rs1196445009 Functional Loss DEL dbSNP153 32..33 33 - - - 57782 RMVar_ID_57782 Human_SNP_ID_453010740 m1A Human chr11 + 695712 695712 695712 GGCCTCGGCCGTGGCTCGGACGTCCGCTCCCGAAACGCGGCGCGGTCGGGCCCCTTCGTCAGGAG GGCCTCGGCCGTGGCTCGGACGTCCGCTCCCGCAACGCGGCGCGGTCGGGCCCCTTCGTCAGGAG A C TMEM80,EPS8L2 Ensembl:ENSG00000177042,Ensembl:ENSG00000177106 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:695576..698897 26863196 MeRIP-seq:(Medium) rs976053924 Functional Loss SNV dbSNP153 33..33 33 - - - 57783 RMVar_ID_57783 Human_SNP_ID_453013418 m1A Human chr11 - 703904 703904 703904 GAATTTGTTTAGCACTCCGTGCAAAAGGCAAAAGCTGATAAAACTGGAGTGGACGGAGGCTCCGA GAATTTGTTTAGCACTCCGTGCAAAAGGCAAACGCTGATAAAACTGGAGTGGACGGAGGCTCCGA T G DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:697796..706616 32194978 MeRIP-seq:(Medium) rs1334597451 Functional Loss SNV dbSNP153 33..33 33 - - - 57784 RMVar_ID_57784 Human_SNP_ID_453013826 m1A Human chr11 + 705155 705155 705155 CTCCCCAGGAAGTGCTCCGGCCAGCCCAGGGTAAACACGCTAGCCCTGCCCCTCTGGGACCATAG CTCCCCAGGAAGTGCTCCGGCCAGCCCAGGGTGAACACGCTAGCCCTGCCCCTCTGGGACCATAG A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:705150..705307 26863196 MeRIP-seq:(Medium) rs1205582130 Functional Loss SNV dbSNP153 33..33 33 - - - 57785 RMVar_ID_57785 Human_SNP_ID_453014718 m1A Human chr11 - 707831 707831 707831 TGTGTCCAGGCACACACCTGGGCGAGACACCAACGCACCCTTGCAGACTCAGGCCTGGGGGCACG TGTGTCCAGGCACACACCTGGGCGAGACACCAGCGCACCCTTGCAGACTCAGGCCTGGGGGCACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:707828..708038 26863196 MeRIP-seq:(Medium) rs768395516 Functional Loss SNV dbSNP153 33..33 33 - - - 57786 RMVar_ID_57786 Human_SNP_ID_453015192 m1A Human chr11 - 709388 709388 709388 CGGACTGGCTCATGGTGTCTTGGGTGGCGGCCAGCGGGAGAAGGGCAGACCTCAGTGTGGCCCCG CGGACTGGCTCATGGTGTCTTGGGTGGCGGCCTGCGGGAGAAGGGCAGACCTCAGTGTGGCCCCG T A AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:709301..709475 26863196 MeRIP-seq:(Medium) rs1188119186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5170025 57787 RMVar_ID_57787 Human_SNP_ID_453015203 m1A Human chr11 + 709401 709401 709401 AGGTCTGCCCTTCTCCCGCTGGCCGCCACCCAAGACACCATGAGCCAGTCCGGGGCCGTGAGCTG AGGTCTGCCCTTCTCCCGCTGGCCGCCACCCAGGACACCATGAGCCAGTCCGGGGCCGTGAGCTG A G EPS8L2 Ensembl:ENSG00000177106 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:709321..709426 26863196 MeRIP-seq:(Medium) rs10902202 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_867010,Human_RBP_ID_18971570 Human_Splice_Rec_1194436,Human_Splice_Rec_1194437,Human_Splice_Rec_1194446,Human_Splice_Rec_1194447,Human_Splice_Rec_1194452,Human_Splice_Rec_1194453,Human_Splice_Rec_1194492,Human_Splice_Rec_1194493,Human_Splice_Rec_1194534,Human_Splice_Rec_1194535,Human_Splice_Rec_1194542,Human_Splice_Rec_1194543,Human_Splice_Rec_1194560,Human_Splice_Rec_1194561,Human_Splice_Rec_1194600,Human_Splice_Rec_1194601,Human_Splice_Rec_1194640,Human_Splice_Rec_1194641,Human_Splice_Rec_1194644,Human_Splice_Rec_1194645,Human_Splice_Rec_1194650,Human_Splice_Rec_1194651,Human_Splice_Rec_1194692,Human_Splice_Rec_1194693,Human_Splice_Rec_1194700,Human_Splice_Rec_1194701,Human_Splice_Rec_1194708,Human_Splice_Rec_1194709,Human_Splice_Rec_1194716,Human_Splice_Rec_1194717,Human_Splice_Rec_1194720,Human_Splice_Rec_1194721,Human_Splice_Rec_1194759 Human_miRNA_ID_2083410 RMVar_hsa_circ_88989,RMVar_hsa_circ_147442 57788 RMVar_ID_57788 Human_SNP_ID_453015286 m1A Human chr11 - 709553 709553 709553 TTGGCCACACCGTCGGACCGGCCCAGGCTGCCACTGCAGGGGAGGGGCTGTCAGGGCAGGGCCAA TTGGCCACACCGTCGGACCGGCCCAGGCTGCCGCTGCAGGGGAGGGGCTGTCAGGGCAGGGCCAA T C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:709551..709650 26863196 MeRIP-seq:(Medium) rs1370098738 Functional Loss SNV dbSNP153 33..33 33 - - - 57789 RMVar_ID_57789 Human_SNP_ID_453015310 m1A Human chr11 + 709584 709584 709584 GTGGCAGCCTGGGCCGGTCCGACGGTGTGGCCAAGATGAGCCCCAAGGACCTGTTTGGTGAGTGA GTGGCAGCCTGGGCCGGTCCGACGGTGTGGCCGAGATGAGCCCCAAGGACCTGTTTGGTGAGTGA A G EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:697895..709590 32194978 MeRIP-seq:(Medium) rs753552500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18973077,Human_RBP_ID_19048892 Human_Splice_Rec_1194438,Human_Splice_Rec_1194439,Human_Splice_Rec_1194448,Human_Splice_Rec_1194454,Human_Splice_Rec_1194455,Human_Splice_Rec_1194494,Human_Splice_Rec_1194495,Human_Splice_Rec_1194536,Human_Splice_Rec_1194537,Human_Splice_Rec_1194544,Human_Splice_Rec_1194545,Human_Splice_Rec_1194562,Human_Splice_Rec_1194563,Human_Splice_Rec_1194602,Human_Splice_Rec_1194642,Human_Splice_Rec_1194646,Human_Splice_Rec_1194647,Human_Splice_Rec_1194652,Human_Splice_Rec_1194653,Human_Splice_Rec_1194694,Human_Splice_Rec_1194695,Human_Splice_Rec_1194702,Human_Splice_Rec_1194703,Human_Splice_Rec_1194710,Human_Splice_Rec_1194711,Human_Splice_Rec_1194718,Human_Splice_Rec_1194722,Human_Splice_Rec_1194723,Human_Splice_Rec_1194760,Human_Splice_Rec_1194761,Human_Splice_Rec_1194797 RMVar_hsa_circ_88989,RMVar_hsa_circ_147442 57790 RMVar_ID_57790 Human_SNP_ID_453015349 m1A Human chr11 - 709680 709679 709680 GGCCAGACCAGGCACAGCTGTGGGGCAGGAGCAGCTGTCCCCCACCTGGATGCAGTGCCCATTTC GGCCAGACCAGGCACAGCTGTGGGGCAGGAGC_GCTGTCCCCCACCTGGATGCAGTGCCCATTTC CT C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:709529..709715 26863196 MeRIP-seq:(Medium) rs1318973894 Functional Loss DEL dbSNP153 33..33 33 - - - 57791 RMVar_ID_57791 Human_SNP_ID_453015350 m1A Human chr11 - 709680 709680 709680 GGCCAGACCAGGCACAGCTGTGGGGCAGGAGCAGCTGTCCCCCACCTGGATGCAGTGCCCATTTC GGCCAGACCAGGCACAGCTGTGGGGCAGGAGCGGCTGTCCCCCACCTGGATGCAGTGCCCATTTC T C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:709529..709715 26863196 MeRIP-seq:(Medium) rs11605783 Functional Loss SNV dbSNP153 33..33 33 - - - 57792 RMVar_ID_57792 Human_SNP_ID_453018767 m1A Human chr11 + 719627 719627 719627 CCTTGGAGTAGCGAGCACGCTGGACGCACAGCACACCACGTGCAGCGCGACGTTGGGTCTGATTC CCTTGGAGTAGCGAGCACGCTGGACGCACAGCGCACCACGTGCAGCGCGACGTTGGGTCTGATTC A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:719622..719827 26863196 MeRIP-seq:(Medium) rs1415859484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17204869 RMVar_hsa_circ_88989,RMVar_hsa_circ_84934,RMVar_hsa_circ_112437,RMVar_hsa_circ_147442,RMVar_hsa_circ_147443,RMVar_hsa_circ_147444,RMVar_hsa_circ_64100 57793 RMVar_ID_57793 Human_SNP_ID_453019455 m1A Human chr11 + 721019 721019 721019 GGAGGGGAGGAGCCCGGCAGGGAGGGAGGGTCAGGTGCGTTCCCGGCGGGGCTGAGCAGGACCCC GGAGGGGAGGAGCCCGGCAGGGAGGGAGGGTCCGGTGCGTTCCCGGCGGGGCTGAGCAGGACCCC A C EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:721018..721148 26863196 MeRIP-seq:(Medium) rs7126891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193875,Human_RBP_ID_5342013,Human_RBP_ID_8173886,Human_RBP_ID_9415181,Human_RBP_ID_18932081,Human_RBP_ID_19048896,Human_RBP_ID_21965060,Human_RBP_ID_22537969,Human_RBP_ID_22642206,Human_RBP_ID_26776052 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_147447 57794 RMVar_ID_57794 Human_SNP_ID_453019456 m1A Human chr11 + 721019 721019 721019 GGAGGGGAGGAGCCCGGCAGGGAGGGAGGGTCAGGTGCGTTCCCGGCGGGGCTGAGCAGGACCCC GGAGGGGAGGAGCCCGGCAGGGAGGGAGGGTCGGGTGCGTTCCCGGCGGGGCTGAGCAGGACCCC A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:721018..721148 26863196 MeRIP-seq:(Medium) rs7126891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193875,Human_RBP_ID_5342013,Human_RBP_ID_8173886,Human_RBP_ID_9415181,Human_RBP_ID_18932081,Human_RBP_ID_19048896,Human_RBP_ID_21965060,Human_RBP_ID_22537969,Human_RBP_ID_22642206,Human_RBP_ID_26776052 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_147447 57795 RMVar_ID_57795 Human_SNP_ID_453019758 m1A Human chr11 + 721567 721567 721567 GGGCTGACCCCTGACCCCCTCTGACCCCAGCAAATCCTCAACTGCGCCCTGGACGACATCGAGTG GGGCTGACCCCTGACCCCCTCTGACCCCAGCACATCCTCAACTGCGCCCTGGACGACATCGAGTG A C EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:721565..721705 26863196 MeRIP-seq:(Medium) rs758045701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867017,Human_RBP_ID_18973089 Human_Splice_Rec_1194468,Human_Splice_Rec_1194508,Human_Splice_Rec_1194558,Human_Splice_Rec_1194576,Human_Splice_Rec_1194614,Human_Splice_Rec_1194666,Human_Splice_Rec_1194736,Human_Splice_Rec_1194774,Human_Splice_Rec_1194812,Human_Splice_Rec_1194820,Human_Splice_Rec_1194824,Human_Splice_Rec_1194832,Human_Splice_Rec_1194836,Human_Splice_Rec_1194860,Human_Splice_Rec_1194868 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_147447 57796 RMVar_ID_57796 Human_SNP_ID_453019912 m1A Human chr11 - 721811 721808 721811 TCTGTCCCACGCAGCCCATCTGTGTGGGCTGGACCTTCCTCCACCTCCATGAGTAGCCCCCATGG TCTGTCCCACGCAGCCCATCTGTGTGGGCTGG___TTCCTCCACCTCCATGAGTAGCCCCCATGG AGGT A AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:721551..721925;chr11:721551..721900 26863196 MeRIP-seq:(Medium) rs774849193 Functional Loss DEL dbSNP153 33..35 33 - - - 57797 RMVar_ID_57797 Human_SNP_ID_453020086 m1A Human chr11 + 722115 722115 722115 ACCCCCAGGCAAAGCTGCAGAAGCACATCCAGAACCCCAGCGCCGCGGAGCTCGTGCACTTCCTC ACCCCCAGGCAAAGCTGCAGAAGCACATCCAGGACCCCAGCGCCGCGGAGCTCGTGCACTTCCTC A G EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:721980..722119 26863196 MeRIP-seq:(Medium) rs1210245734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1194472,Human_Splice_Rec_1194473,Human_Splice_Rec_1194512,Human_Splice_Rec_1194513,Human_Splice_Rec_1194580,Human_Splice_Rec_1194581,Human_Splice_Rec_1194618,Human_Splice_Rec_1194619,Human_Splice_Rec_1194670,Human_Splice_Rec_1194671,Human_Splice_Rec_1194740,Human_Splice_Rec_1194741,Human_Splice_Rec_1194778,Human_Splice_Rec_1194779,Human_Splice_Rec_1194816,Human_Splice_Rec_1194817,Human_Splice_Rec_1194838,Human_Splice_Rec_1194839,Human_Splice_Rec_1194872 Human_miRNA_ID_1545864,Human_miRNA_ID_2684601 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_79540,RMVar_hsa_circ_147447,RMVar_hsa_circ_147448 57798 RMVar_ID_57798 Human_SNP_ID_453020136 m1A Human chr11 + 722185 722185 722185 GCCTCTGGACCTGGTGCCTGGGGCCGGGCGGCAGGGGCGCGCAGGGTGGGGGCCCAGAGGCCTCT GCCTCTGGACCTGGTGCCTGGGGCCGGGCGGCGGGGGCGCGCAGGGTGGGGGCCCAGAGGCCTCT A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:722182..722412 26863196 MeRIP-seq:(Medium) rs896827184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808704,Human_RBP_ID_5343241,Human_RBP_ID_9363254,Human_RBP_ID_18971580,Human_RBP_ID_21965065,Human_RBP_ID_23117919 Human_Splice_Rec_1194472,Human_Splice_Rec_1194512,Human_Splice_Rec_1194580,Human_Splice_Rec_1194618,Human_Splice_Rec_1194670,Human_Splice_Rec_1194740,Human_Splice_Rec_1194778,Human_Splice_Rec_1194816,Human_Splice_Rec_1194838,Human_Splice_Rec_1194872 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_79540,RMVar_hsa_circ_147447,RMVar_hsa_circ_147448 57799 RMVar_ID_57799 Human_SNP_ID_453020165 m1A Human chr11 - 722235 722235 722235 GCCCAAGGCGGGCACCTGCTGCCCCAACCCCGACCCCGGGGAGATGCTGCAGAGGCCTCTGGGCC GCCCAAGGCGGGCACCTGCTGCCCCAACCCCGGCCCCGGGGAGATGCTGCAGAGGCCTCTGGGCC T C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:722189..722435 26863196 MeRIP-seq:(Medium) rs936609609 Functional Loss SNV dbSNP153 33..33 33 - - - 57800 RMVar_ID_57800 Human_SNP_ID_453020324 m1A Human chr11 - 722569 722569 722569 CATGCAGCGCTGGCCCCCCATGAAGCCCCGGCACTGCTCTGCCCTGCCCTACCGGGGCCGCATCC CATGCAGCGCTGGCCCCCCATGAAGCCCCGGCGCTGCTCTGCCCTGCCCTACCGGGGCCGCATCC T C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:722523..722607 26863196 MeRIP-seq:(Medium) rs191126136 Functional Loss SNV dbSNP153 33..33 33 - - - 57801 RMVar_ID_57801 Human_SNP_ID_453020431 m1A Human chr11 + 722797 722797 722797 CCTGGGAGGTGGAGGGGCTGGCGTCTGCCCCCATCGAGGAGGTGAGAGCACCAGCAGCCCCCATC CCTGGGAGGTGGAGGGGCTGGCGTCTGCCCCCGTCGAGGAGGTGAGAGCACCAGCAGCCCCCATC A G EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:722746..722831 26863196 MeRIP-seq:(Medium) rs1411579027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18973102,Human_RBP_ID_22895521 Human_Splice_Rec_1194477,Human_Splice_Rec_1194517,Human_Splice_Rec_1194585,Human_Splice_Rec_1194623,Human_Splice_Rec_1194675,Human_Splice_Rec_1194745,Human_Splice_Rec_1194783,Human_Splice_Rec_1194843,Human_Splice_Rec_1194865,Human_Splice_Rec_1194875,Human_Splice_Rec_1194889 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_79540,RMVar_hsa_circ_147447,RMVar_hsa_circ_147448,RMVar_hsa_circ_10531 57802 RMVar_ID_57802 Human_SNP_ID_453020616 m1A Human chr11 + 723197 723197 723197 CCCCTGTCATATGCCCCCTCGTCCTGGGACCCAGCCCCGCCCCATGTCTAACTCAGGTCGCCCAC CCCCTGTCATATGCCCCCTCGTCCTGGGACCCCGCCCCGCCCCATGTCTAACTCAGGTCGCCCAC A C EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:723195..723325 26863196 MeRIP-seq:(Medium) rs75996321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126428,Human_RBP_ID_22570422,Human_RBP_ID_22642214 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_79540,RMVar_hsa_circ_147447,RMVar_hsa_circ_147448,RMVar_hsa_circ_10531 57803 RMVar_ID_57803 Human_SNP_ID_453020649 m1A Human chr11 + 723292 723292 723292 AGTCCATAAGAAACTCCCAGAAGCACAGCCCCACTTCAGAGCCCACCCCCCCGGGGGATGCCCTA AGTCCATAAGAAACTCCCAGAAGCACAGCCCCGCTTCAGAGCCCACCCCCCCGGGGGATGCCCTA A G EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:723150..723300 26863196 MeRIP-seq:(Medium) rs762876409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1194478,Human_Splice_Rec_1194479,Human_Splice_Rec_1194518,Human_Splice_Rec_1194519,Human_Splice_Rec_1194586,Human_Splice_Rec_1194587,Human_Splice_Rec_1194624,Human_Splice_Rec_1194625,Human_Splice_Rec_1194676,Human_Splice_Rec_1194677,Human_Splice_Rec_1194746,Human_Splice_Rec_1194747,Human_Splice_Rec_1194784,Human_Splice_Rec_1194785,Human_Splice_Rec_1194844,Human_Splice_Rec_1194845,Human_Splice_Rec_1194866,Human_Splice_Rec_1194876,Human_Splice_Rec_1194877,Human_Splice_Rec_1194890,Human_Splice_Rec_1194891 Human_miRNA_ID_1417552,Human_miRNA_ID_2873373,Human_miRNA_ID_2981336,Human_miRNA_ID_3069138 RMVar_hsa_circ_112437,RMVar_hsa_circ_147443,RMVar_hsa_circ_64100,RMVar_hsa_circ_108457,RMVar_hsa_circ_127175,RMVar_hsa_circ_147445,RMVar_hsa_circ_79540,RMVar_hsa_circ_147447,RMVar_hsa_circ_147448,RMVar_hsa_circ_10531 57804 RMVar_ID_57804 Human_SNP_ID_453020650 m1A Human chr11 - 723294 723294 723294 GGTAGGGCATCCCCCGGGGGGGTGGGCTCTGAAGTGGGGCTGTGCTTCTGGGAGTTTCTTATGGA GGTAGGGCATCCCCCGGGGGGGTGGGCTCTGACGTGGGGCTGTGCTTCTGGGAGTTTCTTATGGA T G AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:723208..723302 26863196 MeRIP-seq:(Medium) rs1360888513 Functional Loss SNV dbSNP153 33..33 33 - - - 57805 RMVar_ID_57805 Human_SNP_ID_453021116 m1A Human chr11 - 724831 724831 724831 TCCCCCTCTTGGACCCCGTCCTCCAGCCCCTCACCTCTAGGACCTCATCCTTGAGCACCGATAGC TCCCCCTCTTGGACCCCGTCCTCCAGCCCCTCTCCTCTAGGACCTCATCCTTGAGCACCGATAGC T A AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:724799..724956;chr11:724800..724979 26863196 MeRIP-seq:(Medium) rs762487907 Functional Loss SNV dbSNP153 33..33 33 - - - 57806 RMVar_ID_57806 Human_SNP_ID_453022125 m1A Human chr11 - 726935 726935 726935 CCCTCCTCTGATTCATGGAATGAAACTTGTTCATGAGTTCTTCCAGCTCCGACCCACTTTGCTGC CCCTCCTCTGATTCATGGAATGAAACTTGTTCTTGAGTTCTTCCAGCTCCGACCCACTTTGCTGC T A AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:726902..726982 26863196 MeRIP-seq:(Medium) rs1397490450 Functional Loss SNV dbSNP153 33..33 33 - - - 57807 RMVar_ID_57807 Human_SNP_ID_453022180 m1A Human chr11 - 727006 727006 727006 CTCCATGCATTGTGGGTGGGCTTCCCCTCCGCAGGCCCCAGCCCAAGGCAGCTGGGCCTAGCTGT CTCCATGCATTGTGGGTGGGCTTCCCCTCCGCGGGCCCCAGCCCAAGGCAGCTGGGCCTAGCTGT T C AP006621.4 Ensembl:ENSG00000269915 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:726956..727140 26863196 MeRIP-seq:(Medium) rs1379442948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1194969 57808 RMVar_ID_57808 Human_SNP_ID_453022348 m1A Human chr11 - 727475 727475 727475 GCCCTTGCAGGTGAAGTGTGTGTCGTTCCCCCACTTTCCCCCGAATGGCACCCACGGCCTCCTGC GCCCTTGCAGGTGAAGTGTGTGTCGTTCCCCCCCTTTCCCCCGAATGGCACCCACGGCCTCCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:727424..727544 26863196 MeRIP-seq:(Medium) rs1032240181 Functional Loss SNV dbSNP153 33..33 33 - - - 57809 RMVar_ID_57809 Human_SNP_ID_453029032 m1A Human chr11 + 747488 747488 747488 GCCGCCGCAGACCCCTCGGTCTTGCTATGTCGAGCTCACCCGTGAAGCGTCAGAGGATGGAGTCC GCCGCCGCAGACCCCTCGGTCTTGCTATGTCGCGCTCACCCGTGAAGCGTCAGAGGATGGAGTCC A C TALDO1 Ensembl:ENSG00000177156 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:747426..747639 26863196 MeRIP-seq:(Medium) rs754266881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_274720,Human_RBP_ID_1265861,Human_RBP_ID_1460289,Human_RBP_ID_4178745,Human_RBP_ID_8358947,Human_RBP_ID_9006347,Human_RBP_ID_9321180,Human_RBP_ID_11716021,Human_RBP_ID_18612958,Human_RBP_ID_26897328,Human_RBP_ID_27416164 Human_Splice_Rec_1194971,Human_Splice_Rec_1194981,Human_Splice_Rec_1194983,Human_Splice_Rec_1194995,Human_Splice_Rec_1195005,Human_Splice_Rec_1195011 RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_147449 57810 RMVar_ID_57810 Human_SNP_ID_453029034 m1A Human chr11 - 747491 747491 747491 CGCGGACTCCATCCTCTGACGCTTCACGGGTGAGCTCGACATAGCAAGACCGAGGGGTCTGCGGC CGCGGACTCCATCCTCTGACGCTTCACGGGTGGGCTCGACATAGCAAGACCGAGGGGTCTGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:747426..747989;chr11:747426..747999;chr11:747426..748094 26863196 MeRIP-seq:(Medium) rs765509037 Functional Loss SNV dbSNP153 33..33 33 - - - 57811 RMVar_ID_57811 Human_SNP_ID_453029056 m1A Human chr11 + 747536 747536 747536 GTCAGAGGATGGAGTCCGCGCTGGACCAGCTCAAGCAGTTCACCACCGTGGTGGCCGACACGGGC GTCAGAGGATGGAGTCCGCGCTGGACCAGCTCCAGCAGTTCACCACCGTGGTGGCCGACACGGGC A C TALDO1 Ensembl:ENSG00000177156 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:747487..747600 26863196 MeRIP-seq:(Medium) rs138232181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750560,Human_RBP_ID_1460292,Human_RBP_ID_4184552,Human_RBP_ID_9321180,Human_RBP_ID_22434987,Human_RBP_ID_26803067,Human_RBP_ID_26897329 Human_Splice_Rec_1194971,Human_Splice_Rec_1194981,Human_Splice_Rec_1194983,Human_Splice_Rec_1194995,Human_Splice_Rec_1195005,Human_Splice_Rec_1195011 RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_147449 57812 RMVar_ID_57812 Human_SNP_ID_453029063 m1A Human chr11 + 747545 747545 747545 TGGAGTCCGCGCTGGACCAGCTCAAGCAGTTCACCACCGTGGTGGCCGACACGGGCGACTTCCAC TGGAGTCCGCGCTGGACCAGCTCAAGCAGTTCGCCACCGTGGTGGCCGACACGGGCGACTTCCAC A G TALDO1 Ensembl:ENSG00000177156 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:747473..747600 26863410 MeRIP-seq:(Medium) rs1414426846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_869223,Human_RBP_ID_4184553,Human_RBP_ID_9321180,Human_RBP_ID_22434987,Human_RBP_ID_26803067 Human_Splice_Rec_1194971,Human_Splice_Rec_1194981,Human_Splice_Rec_1194983,Human_Splice_Rec_1194995,Human_Splice_Rec_1195005,Human_Splice_Rec_1195011 RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_147449 57813 RMVar_ID_57813 Human_SNP_ID_453031337 m1A Human chr11 - 755829 755829 755829 AAAAGCCAAAGTAAGTGGAGTACTTGCTTCCAACTGGAAACATGTGAAGGAACCCTGTAATTCCC AAAAGCCAAAGTAAGTGGAGTACTTGCTTCCAGCTGGAAACATGTGAAGGAACCCTGTAATTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:755826..755965 26863196 MeRIP-seq:(Medium) rs917716173 Functional Loss SNV dbSNP153 33..33 33 - - - 57814 RMVar_ID_57814 Human_SNP_ID_453031360 m1A Human chr11 + 755888 755888 755888 GCTTTTGAAAACTATTTCCCTAGCCATCGACGAGTACAAGCCCCAGGATGCTACCACCAACCCGT GCTTTTGAAAACTATTTCCCTAGCCATCGACGGGTACAAGCCCCAGGATGCTACCACCAACCCGT A G TALDO1 Ensembl:ENSG00000177156 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:755876..755950 26863196 MeRIP-seq:(Medium) rs1165057276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227182,Human_RBP_ID_871760,Human_RBP_ID_4178978,Human_RBP_ID_22434127,Human_RBP_ID_26804301 Human_Splice_Rec_1194974,Human_Splice_Rec_1194982,Human_Splice_Rec_1194984,Human_Splice_Rec_1194996,Human_Splice_Rec_1195006,Human_Splice_Rec_1195012 Human_miRNA_ID_2040080,Human_miRNA_ID_3019062 RMVar_hsa_circ_8060,RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_373496,RMVar_hsa_circ_147449,RMVar_hsa_circ_291586,RMVar_hsa_circ_147451,RMVar_hsa_circ_147452 57815 RMVar_ID_57815 Human_SNP_ID_453031402 m1A Human chr11 + 755972 755972 755972 ACAGATGCCCGCTTACCAGGAGCTGGTGGAGGAGGCGATTGCCTATGGCCGGAAGCTGGGCGGGT ACAGATGCCCGCTTACCAGGAGCTGGTGGAGGCGGCGATTGCCTATGGCCGGAAGCTGGGCGGGT A C TALDO1 Ensembl:ENSG00000177156 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:755874..755973 32194978 MeRIP-seq:(Medium) rs376926927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178989,Human_RBP_ID_9361872,Human_RBP_ID_17801408,Human_RBP_ID_22432713,Human_RBP_ID_26317969 Human_Splice_Rec_1194974,Human_Splice_Rec_1194975,Human_Splice_Rec_1194982,Human_Splice_Rec_1194984,Human_Splice_Rec_1194985,Human_Splice_Rec_1194996,Human_Splice_Rec_1194997,Human_Splice_Rec_1195006,Human_Splice_Rec_1195007,Human_Splice_Rec_1195012,Human_Splice_Rec_1195013,Human_Splice_Rec_1195025 RMVar_hsa_circ_8060,RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_373496,RMVar_hsa_circ_147449,RMVar_hsa_circ_291586,RMVar_hsa_circ_147451,RMVar_hsa_circ_147452 57816 RMVar_ID_57816 Human_SNP_ID_453031406 m1A Human chr11 - 755978 755978 755978 GCACTCACCCGCCCAGCTTCCGGCCATAGGCAATCGCCTCCTCCACCAGCTCCTGGTAAGCGGGC GCACTCACCCGCCCAGCTTCCGGCCATAGGCAGTCGCCTCCTCCACCAGCTCCTGGTAAGCGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:755874..756023 32194978 MeRIP-seq:(Medium) rs146282855 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_172 57817 RMVar_ID_57817 Human_SNP_ID_453033760 m1A Human chr11 - 763323 763311 763323 TCCTCGAGCTCCCTGCGGGGCGGGGACAGGTGAGGGCGGGGCAGGTGAGGGCGGGGACAGGTGAG TCCTCGAGCTCCCTGCGGGGCGGGGACAGGTG____________GTGAGGGCGGGGACAGGTGAG CCTGCCCCGCCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:763317..763464 26863196 MeRIP-seq:(Medium) rs1469131031 Functional Loss DEL dbSNP153 33..44 33 - - - 57818 RMVar_ID_57818 Human_SNP_ID_453033781 m1A Human chr11 - 763323 763323 763323 TCCTCGAGCTCCCTGCGGGGCGGGGACAGGTGAGGGCGGGGCAGGTGAGGGCGGGGACAGGTGAG TCCTCGAGCTCCCTGCGGGGCGGGGACAGGTGGGGGCGGGGCAGGTGAGGGCGGGGACAGGTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:763317..763464 26863196 MeRIP-seq:(Medium) rs528127490 Functional Loss SNV dbSNP153 33..33 33 - - - 57819 RMVar_ID_57819 Human_SNP_ID_453033862 m1A Human chr11 + 763432 763432 763432 CCCAGGCTGTGGCCTGTGCCGAGGCGGGTGTGACCCTCATCTCCCCATTTGTTGGGCGCATCCTT CCCAGGCTGTGGCCTGTGCCGAGGCGGGTGTGGCCCTCATCTCCCCATTTGTTGGGCGCATCCTT A G TALDO1 Ensembl:ENSG00000177156 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:760933..763525 32194978 MeRIP-seq:(Medium) rs759782370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404038,Human_RBP_ID_9275391,Human_RBP_ID_17349951,Human_RBP_ID_22034151,Human_RBP_ID_22432717,Human_RBP_ID_22753234 Human_Splice_Rec_1194980,Human_Splice_Rec_1194990,Human_Splice_Rec_1194991,Human_Splice_Rec_1195002,Human_Splice_Rec_1195003,Human_Splice_Rec_1195018,Human_Splice_Rec_1195019 Human_miRNA_ID_841684,Human_miRNA_ID_2065285,Human_miRNA_ID_2367170,Human_miRNA_ID_2703153,Human_miRNA_ID_2934461,Human_miRNA_ID_3014968 RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_109835,RMVar_hsa_circ_147453 57820 RMVar_ID_57820 Human_SNP_ID_453034133 m1A Human chr11 - 763946 763946 763946 GAGCAGGAGCCACAGCTGGGCAGTGGGGCCTCACCCGCCTTGGCTGAGAGCACAGGCACCAGCTT GAGCAGGAGCCACAGCTGGGCAGTGGGGCCTCGCCCGCCTTGGCTGAGAGCACAGGCACCAGCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:763931..764067 32194978 MeRIP-seq:(Medium) rs879177588 Functional Loss SNV dbSNP153 33..33 33 - - - 57821 RMVar_ID_57821 Human_SNP_ID_453034243 m1A Human chr11 + 764300 764300 764300 GGCTGGTTCTTGTCCCCCAGCCCAAGCCAGTGACCTGGAAAAAATCCACCTGGATGAGAAGTCTT GGCTGGTTCTTGTCCCCCAGCCCAAGCCAGTGGCCTGGAAAAAATCCACCTGGATGAGAAGTCTT A G TALDO1 Ensembl:ENSG00000177156 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs779846428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22034161,Human_RBP_ID_22426084,Human_RBP_ID_22434134,Human_RBP_ID_23522041 Human_Splice_Rec_1195022 Human_miRNA_ID_2514692 RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_126484,RMVar_hsa_circ_109835,RMVar_hsa_circ_147453,RMVar_hsa_circ_75799,RMVar_hsa_circ_147454,RMVar_hsa_circ_147455 57822 RMVar_ID_57822 Human_SNP_ID_453036527 m1A Human chr11 - 770705 770705 770705 CTGAGGGGGTGTCGGCTCTCCTGGAGGGTCCAAACCCCCATCCTCCTGCATGTTCTCTGGTAGGA CTGAGGGGGTGTCGGCTCTCCTGGAGGGTCCAGACCCCCATCCTCCTGCATGTTCTCTGGTAGGA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs567149534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404150,Human_RBP_ID_751682,Human_RBP_ID_17682674,Human_RBP_ID_18478260,Human_RBP_ID_18971592,Human_RBP_ID_24903649 Human_Splice_Rec_1195087 Human_miRNA_ID_1024013 RMVar_hsa_circ_69645 57823 RMVar_ID_57823 Human_SNP_ID_453038924 m1A Human chr11 + 777037 777037 777037 CTCCCCACACCCGGGCTCCCCTCTCGCAGCGCAGCGGCCTCAGAGACCAGGCCCAGGCACGCGGC CTCCCCACACCCGGGCTCCCCTCTCGCAGCGCTGCGGCCTCAGAGACCAGGCCCAGGCACGCGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:777031..777134 26863196 MeRIP-seq:(Medium) rs919298918 Functional Loss SNV dbSNP153 33..33 33 - - - 57824 RMVar_ID_57824 Human_SNP_ID_453039115 m1A Human chr11 + 777446 777446 777446 TGGCCACGAGCAGACAGGCGGGCCTGTTAGGGAGCCGCTCGGACGCCATGGCTCGGGCTCGGCGC TGGCCACGAGCAGACAGGCGGGCCTGTTAGGGGGCCGCTCGGACGCCATGGCTCGGGCTCGGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:777259..777475 26863196 MeRIP-seq:(Medium) rs1262110883 Functional Loss SNV dbSNP153 33..33 33 - - - 57825 RMVar_ID_57825 Human_SNP_ID_453039123 m1A Human chr11 - 777452 777452 777452 GACCCAGCGCCGAGCCCGAGCCATGGCGTCCGAGCGGCTCCCTAACAGGCCCGCCTGTCTGCTCG GACCCAGCGCCGAGCCCGAGCCATGGCGTCCGGGCGGCTCCCTAACAGGCCCGCCTGTCTGCTCG T C GATD1 Ensembl:ENSG00000177225 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr11:777333..777500;chr11:777247..777475 26863196 MeRIP-seq:(Medium) rs918075609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752434,Human_RBP_ID_4184558 Human_Splice_Rec_1195047,Human_Splice_Rec_1195061,Human_Splice_Rec_1195075,Human_Splice_Rec_1195097,Human_Splice_Rec_1195109,Human_Splice_Rec_1195121,Human_Splice_Rec_1195135,Human_Splice_Rec_1195149,Human_Splice_Rec_1195163,Human_Splice_Rec_1195173 57826 RMVar_ID_57826 Human_SNP_ID_453039719 m1A Human chr11 + 778927 778927 778927 ACAGATTGAGACTCCTTCTCAAAAAAAAAAAAAAGCCACTGGCCTCTGGCTCCCCCTGGCCCAGC ACAGATTGAGACTCCTTCTCAAAAAAAAAAAAGAGCCACTGGCCTCTGGCTCCCCCTGGCCCAGC A G AP006621.3 Ensembl:ENSG00000255284 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:778924..779197 26863196 MeRIP-seq:(Medium) rs1456082354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9006642,Human_RBP_ID_23155168 57827 RMVar_ID_57827 Human_SNP_ID_453043682 m1A Human chr11 + 790757 790757 790757 TCAGGGTCTGTCACCAACACGATCACATGGCCAGGGCGGGGCAGGGAGAGCTTCGGCTCACAGCA TCAGGGTCTGTCACCAACACGATCACATGGCCGGGGCGGGGCAGGGAGAGCTTCGGCTCACAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:790708..790938 26863196 MeRIP-seq:(Medium) rs907123054 Functional Loss SNV dbSNP153 33..33 33 - - - 57828 RMVar_ID_57828 Human_SNP_ID_453043702 m1A Human chr11 - 790802 790802 790802 GACCACACTTCAGAAGCCCCATCCCCCCTGCCACCGGGCGATCCCTGCTGTGAGCCGAAGCTCTC GACCACACTTCAGAAGCCCCATCCCCCCTGCCGCCGGGCGATCCCTGCTGTGAGCCGAAGCTCTC T C SLC25A22 Ensembl:ENSG00000177542 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:790751..790879 26863196 MeRIP-seq:(Medium) rs1343701703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8174876,Human_RBP_ID_17073594,Human_RBP_ID_23523213 57829 RMVar_ID_57829 Human_SNP_ID_453045127 m1A Human chr11 - 794309 794309 794309 CGTGGACGTGTTTGTGGGGGCTGTGCCTGTGCAGGGGGGACTGGATCTCTGGTGAGTGGTAGTTC CGTGGACGTGTTTGTGGGGGCTGTGCCTGTGCTGGGGGGACTGGATCTCTGGTGAGTGGTAGTTC T A SLC25A22 Ensembl:ENSG00000177542 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:794299..794437 26863196 MeRIP-seq:(Medium) rs767642562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19054434 57830 RMVar_ID_57830 Human_SNP_ID_453045457 m1A Human chr11 - 794903 794902 794904 AAGGAAGCCGGTCCTGACACCCCTGTCCACACAGCCTGCCAGCCAAGCTCATCAATGGCGGCATC AAGGAAGCCGGTCCTGACACCCCTGTCCACA__GCCTGCCAGCCAAGCTCATCAATGGCGGCATC CTG C SLC25A22 Ensembl:ENSG00000177542 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:794857..795043 32194978 MeRIP-seq:(Medium) rs1364367954 Functional Loss DEL dbSNP153 32..33 33 - - - 57831 RMVar_ID_57831 Human_SNP_ID_453045519 m1A Human chr11 + 795024 794999 795025 CTGCTTATCAGCCATTTAACTCGATTGCACCCAGGTAGGAGCCGCAGAGGTGGACGCCAGGCCAG CTGCTTAT__________________________GTAGGAGCCGCAGAGGTGGACGCCAGGCCAG TCAGCCATTTAACTCGATTGCACCCAG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:794984..795162 26863196 MeRIP-seq:(Medium) rs1291555677 Functional Loss DEL dbSNP153 9..34 33 - - - 57832 RMVar_ID_57832 Human_SNP_ID_453046002 m1A Human chr11 + 796047 796047 796047 CCCCCCAGAGGCCAGCTGTTTCACCCACCGGCAGCGCCGTTGCCCAGGGCCACGCGGCTGGCTCA CCCCCCAGAGGCCAGCTGTTTCACCCACCGGCGGCGCCGTTGCCCAGGGCCACGCGGCTGGCTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:796041..796221 26863196 MeRIP-seq:(Medium) rs1057522653 Functional Loss SNV dbSNP153 33..33 33 - - - 57833 RMVar_ID_57833 Human_SNP_ID_453046711 m1A Human chr11 + 798143 798143 798143 TTCGGGCAGCTGTCACCTCCCTCGGCCGCCGCAGCACCTCTCGCCCCCGCAGCCCGGCCGCGTTC TTCGGGCAGCTGTCACCTCCCTCGGCCGCCGCGGCACCTCTCGCCCCCGCAGCCCGGCCGCGTTC A G PANO1 Ensembl:ENSG00000274897 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:798139..798253 26863196 MeRIP-seq:(Medium) rs912154233 Functional Loss SNV dbSNP153 33..33 33 - - - 57834 RMVar_ID_57834 Human_SNP_ID_453047150 m1A Human chr11 + 799293 799293 799293 CCCATCCACTGGGGAATATCTGGGCCAGCCTAAAAGTCTGTGGGGCCTAGGCCTGGGCAGGCTCT CCCATCCACTGGGGAATATCTGGGCCAGCCTAGAAGTCTGTGGGGCCTAGGCCTGGGCAGGCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:799242..799490 26863196 MeRIP-seq:(Medium) rs766735943 Functional Loss SNV dbSNP153 33..33 33 - - - 57835 RMVar_ID_57835 Human_SNP_ID_453047418 m1A Human chr11 + 799830 799830 799830 GGCAGTGGGAGCCTCACCGGAACTCGTGCCGGATGCGCTGCACCTCCCGGTAGGACACCCCCAGG GGCAGTGGGAGCCTCACCGGAACTCGTGCCGGGTGCGCTGCACCTCCCGGTAGGACACCCCCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:799824..800024 32194978 MeRIP-seq:(Medium) rs947639455 Functional Loss SNV dbSNP153 33..33 33 - - - 57836 RMVar_ID_57836 Human_SNP_ID_453047579 m1A Human chr11 + 800149 800149 800149 TCCCTCAGTCCCACCGGCAGCTTGATGGGCAGAGTGGCCATCCACAGGGCGTCTGCGCCCTTCCT TCCCTCAGTCCCACCGGCAGCTTGATGGGCAGGGTGGCCATCCACAGGGCGTCTGCGCCCTTCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:800123..800361 32194978 MeRIP-seq:(Medium) rs765357677 Functional Loss SNV dbSNP153 33..33 33 - - - 57837 RMVar_ID_57837 Human_SNP_ID_453047580 m1A Human chr11 + 800149 800149 800149 TCCCTCAGTCCCACCGGCAGCTTGATGGGCAGAGTGGCCATCCACAGGGCGTCTGCGCCCTTCCT TCCCTCAGTCCCACCGGCAGCTTGATGGGCAGTGTGGCCATCCACAGGGCGTCTGCGCCCTTCCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:800123..800361 32194978 MeRIP-seq:(Medium) rs765357677 Functional Loss SNV dbSNP153 33..33 33 - - - 57838 RMVar_ID_57838 Human_SNP_ID_453048889 m1A Human chr11 - 802379 802379 802379 TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCAAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCTAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC T A PIDD1 Ensembl:ENSG00000177595 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10902221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3938810,Human_RBP_ID_9361879,Human_RBP_ID_18973142 Human_Splice_Rec_1195524,Human_Splice_Rec_1195548,Human_Splice_Rec_1195574,Human_Splice_Rec_1195602,Human_Splice_Rec_1195624,Human_Splice_Rec_1195648,Human_Splice_Rec_1195664 GWAS_ID_6805,GWAS_ID_6806,GWAS_ID_6807,GWAS_ID_6808,GWAS_ID_6809,GWAS_ID_6810,GWAS_ID_6811,GWAS_ID_6812 57839 RMVar_ID_57839 Human_SNP_ID_453048890 m1A Human chr11 - 802379 802379 802379 TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCAAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCGAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC T C PIDD1 Ensembl:ENSG00000177595 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10902221 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3938810,Human_RBP_ID_9361879,Human_RBP_ID_18973142 Human_Splice_Rec_1195524,Human_Splice_Rec_1195548,Human_Splice_Rec_1195574,Human_Splice_Rec_1195602,Human_Splice_Rec_1195624,Human_Splice_Rec_1195648,Human_Splice_Rec_1195664 GWAS_ID_6805,GWAS_ID_6806,GWAS_ID_6807,GWAS_ID_6808,GWAS_ID_6809,GWAS_ID_6810,GWAS_ID_6811,GWAS_ID_6812 57840 RMVar_ID_57840 Human_SNP_ID_453048891 m1A Human chr11 - 802379 802379 802379 TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCAAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCCAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC T G PIDD1 Ensembl:ENSG00000177595 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10902221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3938810,Human_RBP_ID_9361879,Human_RBP_ID_18973142 Human_Splice_Rec_1195524,Human_Splice_Rec_1195548,Human_Splice_Rec_1195574,Human_Splice_Rec_1195602,Human_Splice_Rec_1195624,Human_Splice_Rec_1195648,Human_Splice_Rec_1195664 GWAS_ID_6805,GWAS_ID_6806,GWAS_ID_6807,GWAS_ID_6808,GWAS_ID_6809,GWAS_ID_6810,GWAS_ID_6811,GWAS_ID_6812 57841 RMVar_ID_57841 Human_SNP_ID_453049856 m1A Human chr11 - 804379 804379 804379 CCTCCAAGGACCGTCGGTGGGCGATGGCTGCAACGGTGGAGGGGCCAGAGCTGGAGGCAGCTGCT CCTCCAAGGACCGTCGGTGGGCGATGGCTGCAGCGGTGGAGGGGCCAGAGCTGGAGGCAGCTGCT T C PIDD1 Ensembl:ENSG00000177595 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:804331..804408 26863196 MeRIP-seq:(Medium) rs1338878660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9361881,Human_RBP_ID_18433249,Human_RBP_ID_18971621 Human_Splice_Rec_1195594,Human_Splice_Rec_1195644,Human_Splice_Rec_1195660,Human_Splice_Rec_1195688 57842 RMVar_ID_57842 Human_SNP_ID_453051897 m1A Human chr11 - 810020 810014 810020 TCACCACACTCACGCGGCGGCGTCTGCGGCGGAGGCGGCGGAGAAGTCTCACGCGTGCGACCTCG TCACCACACTCACGCGGCGGCGTCTGCGGCGG______CGGAGAAGTCTCACGCGTGCGACCTCG GCCGCCT G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:809951..810404 26863410 MeRIP-seq:(Medium) rs1461351863 Functional Loss DEL dbSNP153 33..38 33 - - - 57843 RMVar_ID_57843 Human_SNP_ID_453051903 m1A Human chr11 - 810020 810020 810020 TCACCACACTCACGCGGCGGCGTCTGCGGCGGAGGCGGCGGAGAAGTCTCACGCGTGCGACCTCG TCACCACACTCACGCGGCGGCGTCTGCGGCGGCGGCGGCGGAGAAGTCTCACGCGTGCGACCTCG T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:809951..810404 26863410 MeRIP-seq:(Medium) rs1013373191 Functional Loss SNV dbSNP153 33..33 33 - - - 57844 RMVar_ID_57844 Human_SNP_ID_453052912 m1A Human chr11 + 812326 812326 812326 GGCAGGCAGTGTGGGCCTAATTCCTAGAAGGCAAGTCCCTGGATAGGAAAGGTGGGGAAGAGAAG GGCAGGCAGTGTGGGCCTAATTCCTAGAAGGCGAGTCCCTGGATAGGAAAGGTGGGGAAGAGAAG A G RPLP2 Ensembl:ENSG00000177600 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:812322..812421 26863196 MeRIP-seq:(Medium) rs1426580020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9006772 RMVar_hsa_circ_31950,RMVar_hsa_circ_120996,RMVar_hsa_circ_147464,RMVar_hsa_circ_147465,RMVar_hsa_circ_80331,RMVar_hsa_circ_89889,RMVar_hsa_circ_147466,RMVar_hsa_circ_147468,RMVar_hsa_circ_125818,RMVar_hsa_circ_147467 57845 RMVar_ID_57845 Human_SNP_ID_453052957 m1A Human chr11 - 812488 812488 812488 GAGGTGAGACCAGAGCAGCTGCCCAGCCTGGGAGGCTGTTCCACAGGGAAGTTAGATGGCACCAG GAGGTGAGACCAGAGCAGCTGCCCAGCCTGGGTGGCTGTTCCACAGGGAAGTTAGATGGCACCAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:812487..812807 26863196 MeRIP-seq:(Medium) rs776638397 Functional Loss SNV dbSNP153 33..33 33 - - - 57846 RMVar_ID_57846 Human_SNP_ID_453055375 m1A Human chr11 + 819615 819615 819615 CTCCGCCAGCGGGGACCCCGAGCTAGAGCCGCAGCGGGACCTGCCCGGCCCCCGGCTCCAGCGAG CTCCGCCAGCGGGGACCCCGAGCTAGAGCCGCGGCGGGACCTGCCCGGCCCCCGGCTCCAGCGAG A G PNPLA2 Ensembl:ENSG00000177666 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:819576..819769 26863196 MeRIP-seq:(Medium) rs1358079229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228032,Human_RBP_ID_752435,Human_RBP_ID_4183881,Human_RBP_ID_5344714,Human_RBP_ID_9321194,Human_RBP_ID_18416496 Human_Splice_Rec_1195734 57847 RMVar_ID_57847 Human_SNP_ID_453055532 m1A Human chr11 - 819970 819970 819970 CGACTCGCCGCGGGGCCCCTCCGCTCACGGAGACCATCCCCCGGCCCCGCACGGCCTTCCCGCCA CGACTCGCCGCGGGGCCCCTCCGCTCACGGAGGCCATCCCCCGGCCCCGCACGGCCTTCCCGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:819919..820247 26863196 MeRIP-seq:(Medium) rs1394089303 Functional Loss SNV dbSNP153 33..33 33 - - - 57848 RMVar_ID_57848 Human_SNP_ID_453055540 m1A Human chr11 - 820004 820004 820004 AGGCGCGGACCGGAACCCTCCCCACGGTACCCACCGACTCGCCGCGGGGCCCCTCCGCTCACGGA AGGCGCGGACCGGAACCCTCCCCACGGTACCCGCCGACTCGCCGCGGGGCCCCTCCGCTCACGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:819890..820147 26863196 MeRIP-seq:(Medium) rs1276721865 Functional Loss SNV dbSNP153 33..33 33 - - - 57849 RMVar_ID_57849 Human_SNP_ID_453056321 m1A Human chr11 + 822508 822505 822508 GCGAGAGTGACATCTGTCCGCAGGACAGCTCCACCAACATCCACGAGCTGCGGGTCACCAACACC GCGAGAGTGACATCTGTCCGCAGGACAGCT___CCAACATCCACGAGCTGCGGGTCACCAACACC TCCA T PNPLA2 Ensembl:ENSG00000177666 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:822459..822560 26863196 MeRIP-seq:(Medium) rs749881826 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_404733,Human_RBP_ID_751704,Human_RBP_ID_6098755,Human_RBP_ID_17233251,Human_RBP_ID_26803103,Human_RBP_ID_26898109 Human_Splice_Rec_1195741,Human_Splice_Rec_1195755,Human_Splice_Rec_1195763 RMVar_hsa_circ_46024 57850 RMVar_ID_57850 Human_SNP_ID_453056747 m1A Human chr11 - 823589 823589 823589 CCCACCCCGCCCTCTCCCGCCCGGGTCCGCGCACCGTTCCGCTGCAGAAAGCGCAGGCCATCCCG CCCACCCCGCCCTCTCCCGCCCGGGTCCGCGCGCCGTTCCGCTGCAGAAAGCGCAGGCCATCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:823585..823705 26863196 MeRIP-seq:(Medium) rs777539013 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_173 57851 RMVar_ID_57851 Human_SNP_ID_453056773 m1A Human chr11 + 823607 823607 823607 CTGCAGCGGAACGGTGCGCGGACCCGGGCGGGAGAGGGCGGGGTGGGCTCGGCTCTGCTACCCCC CTGCAGCGGAACGGTGCGCGGACCCGGGCGGGGGAGGGCGGGGTGGGCTCGGCTCTGCTACCCCC A G PNPLA2 Ensembl:ENSG00000177666 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:823601..823696 26863196 MeRIP-seq:(Medium) rs760836201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344724,Human_RBP_ID_19048945,Human_RBP_ID_22642231 Human_Splice_Rec_1195742,Human_Splice_Rec_1195756,Human_Splice_Rec_1195764 RMVar_hsa_circ_49021 57852 RMVar_ID_57852 Human_SNP_ID_453056877 m1A Human chr11 + 823745 823745 823745 CCCCTTGCTGGCGTTGCCCCCCGCCCGCCCCCACGGCCCAGAGGACAAGGACCAGGCAGTGGAGA CCCCTTGCTGGCGTTGCCCCCCGCCCGCCCCCCCGGCCCAGAGGACAAGGACCAGGCAGTGGAGA A C PNPLA2 Ensembl:ENSG00000177666 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1436895164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9275394 Human_Splice_Rec_1195744,Human_Splice_Rec_1195766 RMVar_hsa_circ_49021 57853 RMVar_ID_57853 Human_SNP_ID_453057600 m1A Human chr11 - 824806 824805 824806 GGGCCGGGCCTCGGGAGCAGGGGTGCTCAGCAAGGGGGCAGGCCCGGCCAGCTGGTGCTGCGGGG GGGCCGGGCCTCGGGAGCAGGGGTGCTCAGCAGAGGGGCAGGCCCGGCCAGCTGGTGCTGCGGGG CT TC AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:824456..830573 26863410 MeRIP-seq:(Medium) rs886038654 Functional Loss MNV dbSNP153 33..34 33 - - - 57854 RMVar_ID_57854 Human_SNP_ID_453057604 m1A Human chr11 - 824806 824806 824806 GGGCCGGGCCTCGGGAGCAGGGGTGCTCAGCAAGGGGGCAGGCCCGGCCAGCTGGTGCTGCGGGG GGGCCGGGCCTCGGGAGCAGGGGTGCTCAGCAGGGGGGCAGGCCCGGCCAGCTGGTGCTGCGGGG T C AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:824456..830573 26863410 MeRIP-seq:(Medium) rs541287299 Functional Loss SNV dbSNP153 33..33 33 - - - 57855 RMVar_ID_57855 Human_SNP_ID_453057640 m1A Human chr11 - 824852 824852 824852 GTTCCTCGAGAGGGTCGGGGTCTCACAGCCCCAGGGCCCCGATCACGGGCCGGGCCTCGGGAGCA GTTCCTCGAGAGGGTCGGGGTCTCACAGCCCCTGGGCCCCGATCACGGGCCGGGCCTCGGGAGCA T A AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:824801..824900 26863196 MeRIP-seq:(Medium) rs1262777413 Functional Loss SNV dbSNP153 33..33 33 - - - 57856 RMVar_ID_57856 Human_SNP_ID_453057723 m1A Human chr11 - 825021 825021 825021 CACAGGTGCGCGGGGCCTCAGCGGCCCAGGGGAGGGGTGTGGAAACCTCCCCTCTCAGTGCATGC CACAGGTGCGCGGGGCCTCAGCGGCCCAGGGGTGGGGTGTGGAAACCTCCCCTCTCAGTGCATGC T A AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:824972..825091 26863196 MeRIP-seq:(Medium) rs1335069036 Functional Loss SNV dbSNP153 33..33 33 - - - 57857 RMVar_ID_57857 Human_SNP_ID_453060163 m1A Human chr11 - 830984 830984 830984 GGCGGCCTCGTGCTTCGCTCTCCAGCCTGCGGATCTGCTCCTGCGCCCCCTCCAGCTGCGTTCGC GGCGGCCTCGTGCTTCGCTCTCCAGCCTGCGGTTCTGCTCCTGCGCCCCCTCCAGCTGCGTTCGC T A AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:830953..831038 26863196 MeRIP-seq:(Medium) rs1389667003 Functional Loss SNV dbSNP153 33..33 33 - - - 57858 RMVar_ID_57858 Human_SNP_ID_453061634 m1A Human chr11 + 834497 834497 834497 CCGGCCCACTCTGGCCCTTGGGCCAGACCTGTAACCTGTGACCTGACATGTCCTTGCCCCTCTAG CCGGCCCACTCTGGCCCTTGGGCCAGACCTGTCACCTGTGACCTGACATGTCCTTGCCCCTCTAG A C CD151 Ensembl:ENSG00000177697 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:834495..834664 26863196 MeRIP-seq:(Medium) rs1403348747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22414422 Human_Splice_Rec_1195879,Human_Splice_Rec_1195893,Human_Splice_Rec_1195905,Human_Splice_Rec_1195935,Human_Splice_Rec_1195965,Human_Splice_Rec_1195979,Human_Splice_Rec_1195998,Human_Splice_Rec_1195999,Human_Splice_Rec_1196005,Human_Splice_Rec_1196009,Human_Splice_Rec_1196039,Human_Splice_Rec_1196055 RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472 57859 RMVar_ID_57859 Human_SNP_ID_453062297 m1A Human chr11 - 836056 836056 836056 TCTCGTTGAACTCACCCATCCTGGGGCTGAGGAGGCAGGGGAGGGGTCAGCGGGGCCACAGCACC TCTCGTTGAACTCACCCATCCTGGGGCTGAGGTGGCAGGGGAGGGGTCAGCGGGGCCACAGCACC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:836051..836125 26863196 MeRIP-seq:(Medium) rs759650623 Functional Loss SNV dbSNP153 33..33 33 - - - 57860 RMVar_ID_57860 Human_SNP_ID_453062411 m1A Human chr11 + 836300 836298 836300 CATGGCAGTGGGCATCTGGACGCTGGCCCTCAAGAGTGACTACATCAGCCTGCTGGCCTCAGGCA CATGGCAGTGGGCATCTGGACGCTGGCCCTC__GAGTGACTACATCAGCCTGCTGGCCTCAGGCA CAA C CD151 Ensembl:ENSG00000177697 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:836208..836377 26863196 MeRIP-seq:(Medium) rs1218473834 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4180647,Human_RBP_ID_8360172,Human_RBP_ID_9363277,Human_RBP_ID_22433345,Human_RBP_ID_23206796,Human_RBP_ID_26407556,Human_RBP_ID_26898340,Human_RBP_ID_27207792 Human_Splice_Rec_1195882,Human_Splice_Rec_1195896,Human_Splice_Rec_1195908,Human_Splice_Rec_1195922,Human_Splice_Rec_1195938,Human_Splice_Rec_1195954,Human_Splice_Rec_1195958,Human_Splice_Rec_1195968,Human_Splice_Rec_1195984,Human_Splice_Rec_1195996,Human_Splice_Rec_1196002,Human_Splice_Rec_1196012,Human_Splice_Rec_1196026,Human_Splice_Rec_1196036,Human_Splice_Rec_1196042,Human_Splice_Rec_1196058,Human_Splice_Rec_1196072,Human_Splice_Rec_1196076,Human_Splice_Rec_1196084 Human_miRNA_ID_2865564,Human_miRNA_ID_2996381 RMVar_hsa_circ_84629,RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472,RMVar_hsa_circ_101560,RMVar_hsa_circ_86893,RMVar_hsa_circ_147473,RMVar_hsa_circ_375673,RMVar_hsa_circ_147476,RMVar_hsa_circ_92006,RMVar_hsa_circ_147477,RMVar_hsa_circ_147475,RMVar_hsa_circ_147478 57861 RMVar_ID_57861 Human_SNP_ID_453062460 m1A Human chr11 + 836417 836417 836417 GACTGGGGTCTTGGGCTGCTGCGCCACCTTCAAGGAGCGTCGGAACCTGCTGCGCCTGGTCAGGA GACTGGGGTCTTGGGCTGCTGCGCCACCTTCAGGGAGCGTCGGAACCTGCTGCGCCTGGTCAGGA A G CD151 Ensembl:ENSG00000177697 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:836036..836450 32194978 MeRIP-seq:(Medium) rs150909098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109910,Human_RBP_ID_808363,Human_RBP_ID_9361886,Human_RBP_ID_22433346,Human_RBP_ID_22753242,Human_RBP_ID_26317989,Human_RBP_ID_27416592 Human_Splice_Rec_1195883,Human_Splice_Rec_1195897,Human_Splice_Rec_1195909,Human_Splice_Rec_1195923,Human_Splice_Rec_1195939,Human_Splice_Rec_1195959,Human_Splice_Rec_1195985,Human_Splice_Rec_1196027,Human_Splice_Rec_1196043,Human_Splice_Rec_1196059,Human_Splice_Rec_1196077 Human_miRNA_ID_596518,Human_miRNA_ID_2221805,Human_miRNA_ID_3073238 RMVar_hsa_circ_84629,RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472,RMVar_hsa_circ_101560,RMVar_hsa_circ_86893,RMVar_hsa_circ_147473,RMVar_hsa_circ_375673,RMVar_hsa_circ_147476,RMVar_hsa_circ_92006,RMVar_hsa_circ_147477,RMVar_hsa_circ_147475,RMVar_hsa_circ_147478 57862 RMVar_ID_57862 Human_SNP_ID_453063272 m1A Human chr11 + 838164 838163 838165 GGTCTTTGGCATGATCTTCACGTGCTGCCTGTACAGGAGTCTCAAGCTGGAGCACTACTGACCCT GGTCTTTGGCATGATCTTCACGTGCTGCCTGT__AGGAGTCTCAAGCTGGAGCACTACTGACCCT TAC T CD151 Ensembl:ENSG00000177697 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:837251..839769 32194978 MeRIP-seq:(Medium) rs777122361 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_404945,Human_RBP_ID_1783178,Human_RBP_ID_5110691,Human_RBP_ID_17648908,Human_RBP_ID_17802323,Human_RBP_ID_18613713,Human_RBP_ID_18971636,Human_RBP_ID_22433351,Human_RBP_ID_22753249 Human_Splice_Rec_1195918,Human_Splice_Rec_1195932,Human_Splice_Rec_1195948,Human_Splice_Rec_1195976,Human_Splice_Rec_1196020,Human_Splice_Rec_1196052,Human_Splice_Rec_1196068 Human_miRNA_ID_1398730,Human_miRNA_ID_2717437 RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472,RMVar_hsa_circ_101560,RMVar_hsa_circ_86893,RMVar_hsa_circ_147473,RMVar_hsa_circ_147477,RMVar_hsa_circ_76911,RMVar_hsa_circ_100252,RMVar_hsa_circ_147480,RMVar_hsa_circ_98985,RMVar_hsa_circ_80869,RMVar_hsa_circ_91719,RMVar_hsa_circ_123734,RMVar_hsa_circ_147481,RMVar_hsa_circ_147482,RMVar_hsa_circ_93869,RMVar_hsa_circ_147483,RMVar_hsa_circ_147484,RMVar_hsa_circ_147485,RMVar_hsa_circ_83961,RMVar_hsa_circ_147486,RMVar_hsa_circ_147487 57863 RMVar_ID_57863 Human_SNP_ID_453063304 m1A Human chr11 + 838225 838225 838225 CCCTGCCTTGGGCCTTGCTGCTGCTGCACCCAACTACTGAGCTGAGACCACTGAGTACCAGGGGC CCCTGCCTTGGGCCTTGCTGCTGCTGCACCCAGCTACTGAGCTGAGACCACTGAGTACCAGGGGC A G CD151 Ensembl:ENSG00000177697 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:838175..838326 26863196 MeRIP-seq:(Medium) rs748660774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404946,Human_RBP_ID_749364,Human_RBP_ID_869202,Human_RBP_ID_9007060,Human_RBP_ID_17648909,Human_RBP_ID_22432728,Human_RBP_ID_22754520,Human_RBP_ID_27417630 Human_Splice_Rec_1195918,Human_Splice_Rec_1195932,Human_Splice_Rec_1195948,Human_Splice_Rec_1195976,Human_Splice_Rec_1196020,Human_Splice_Rec_1196052,Human_Splice_Rec_1196068 Human_miRNA_ID_500895,Human_miRNA_ID_508115,Human_miRNA_ID_830529,Human_miRNA_ID_2173571,Human_miRNA_ID_2177015,Human_miRNA_ID_2355511 RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472,RMVar_hsa_circ_101560,RMVar_hsa_circ_86893,RMVar_hsa_circ_147473,RMVar_hsa_circ_147477,RMVar_hsa_circ_76911,RMVar_hsa_circ_100252,RMVar_hsa_circ_147480,RMVar_hsa_circ_98985,RMVar_hsa_circ_80869,RMVar_hsa_circ_91719,RMVar_hsa_circ_123734,RMVar_hsa_circ_147481,RMVar_hsa_circ_147482,RMVar_hsa_circ_93869,RMVar_hsa_circ_147483,RMVar_hsa_circ_147484,RMVar_hsa_circ_147485,RMVar_hsa_circ_83961,RMVar_hsa_circ_147486,RMVar_hsa_circ_147487 57864 RMVar_ID_57864 Human_SNP_ID_453063434 m1A Human chr11 + 838630 838630 838630 CCTTGGGCCTGGGCCTCTGCCCCTCCCAACCCAGCCCTCGTCTCCCTCGACAGCGCCCCTGCTGT CCTTGGGCCTGGGCCTCTGCCCCTCCCAACCCGGCCCTCGTCTCCCTCGACAGCGCCCCTGCTGT A G CD151 Ensembl:ENSG00000177697 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:838580..838736 26863196 MeRIP-seq:(Medium) rs1188751622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404959,Human_RBP_ID_8174881,Human_RBP_ID_17648913,Human_RBP_ID_18932100,Human_RBP_ID_26407576 RMVar_hsa_circ_85145,RMVar_hsa_circ_106249,RMVar_hsa_circ_147471,RMVar_hsa_circ_147472,RMVar_hsa_circ_101560,RMVar_hsa_circ_86893,RMVar_hsa_circ_147473,RMVar_hsa_circ_147477,RMVar_hsa_circ_76911,RMVar_hsa_circ_100252,RMVar_hsa_circ_147480,RMVar_hsa_circ_98985,RMVar_hsa_circ_80869,RMVar_hsa_circ_91719,RMVar_hsa_circ_123734,RMVar_hsa_circ_147481,RMVar_hsa_circ_147482,RMVar_hsa_circ_93869,RMVar_hsa_circ_147483,RMVar_hsa_circ_147484,RMVar_hsa_circ_147485,RMVar_hsa_circ_83961,RMVar_hsa_circ_105259,RMVar_hsa_circ_147486,RMVar_hsa_circ_147487,RMVar_hsa_circ_147488 57865 RMVar_ID_57865 Human_SNP_ID_453064796 m1A Human chr11 + 842448 842448 842448 CTCGGTGTACTCGGCCTGCAGCAGCCCCAGGTAAGCCTCCCACTTGTTGCCGACGATCTTGCCAC CTCGGTGTACTCGGCCTGCAGCAGCCCCAGGTGAGCCTCCCACTTGTTGCCGACGATCTTGCCAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:842428..842545 26863410 MeRIP-seq:(Medium) rs1352766798 Functional Loss SNV dbSNP153 33..33 33 - - - 57866 RMVar_ID_57866 Human_SNP_ID_453064797 m1A Human chr11 + 842448 842448 842448 CTCGGTGTACTCGGCCTGCAGCAGCCCCAGGTAAGCCTCCCACTTGTTGCCGACGATCTTGCCAC CTCGGTGTACTCGGCCTGCAGCAGCCCCAGGTTAGCCTCCCACTTGTTGCCGACGATCTTGCCAC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:842428..842545 26863410 MeRIP-seq:(Medium) rs1352766798 Functional Loss SNV dbSNP153 33..33 33 - - - 57867 RMVar_ID_57867 Human_SNP_ID_453064802 m1A Human chr11 - 842462 842462 842462 ACGCTGCTTCACTTGTGGCAAGATCGTCGGCAACAAGTGGGAGGCTTACCTGGGGCTGCTGCAGG ACGCTGCTTCACTTGTGGCAAGATCGTCGGCAGCAAGTGGGAGGCTTACCTGGGGCTGCTGCAGG T C POLR2L Ensembl:ENSG00000177700 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:840413..842525 26863196 MeRIP-seq:(Medium) rs377218898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404995,Human_RBP_ID_1163683,Human_RBP_ID_1460776,Human_RBP_ID_4180729,Human_RBP_ID_5110692,Human_RBP_ID_5313487,Human_RBP_ID_9321212,Human_RBP_ID_11732123,Human_RBP_ID_17802337,Human_RBP_ID_18613735,Human_RBP_ID_22432730,Human_RBP_ID_22792366,Human_RBP_ID_26407598,Human_RBP_ID_26898372,Human_RBP_ID_27207818,Human_RBP_ID_27416603 Human_Splice_Rec_1196091,Human_Splice_Rec_1196095 RMVar_hsa_circ_268808 57868 RMVar_ID_57868 Human_SNP_ID_453064813 m1A Human chr11 + 842479 842479 842479 TAAGCCTCCCACTTGTTGCCGACGATCTTGCCACAAGTGAAGCAGCGTACAGGGATGATCATGGC TAAGCCTCCCACTTGTTGCCGACGATCTTGCCGCAAGTGAAGCAGCGTACAGGGATGATCATGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:840451..842525;chr11:840266..842751;chr11:840251..842550 26863196 MeRIP-seq:(Medium) rs1423838343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11732122 57869 RMVar_ID_57869 Human_SNP_ID_453064956 m1A Human chr11 - 842627 842627 842627 GCGGTGGCGGGGCCGGTGGAGGGACGGCCGGAACAGCGGAGAACGAGCGGAGCCGATTCTCCCGC GCGGTGGCGGGGCCGGTGGAGGGACGGCCGGAGCAGCGGAGAACGAGCGGAGCCGATTCTCCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:842576..842766 26863196 MeRIP-seq:(Medium) rs9705236 Functional Loss SNV dbSNP153,PGA 33..33 33 - - - 57870 RMVar_ID_57870 Human_SNP_ID_453065103 m1A Human chr11 + 842902 842902 842902 GCTGCGCGGCGGGAGCGGGCGGCGCGAGCGGGAGGCGGCGGCGCAGGTACTGCGCCTGGGGGTTG GCTGCGCGGCGGGAGCGGGCGGCGCGAGCGGGCGGCGGCGGCGCAGGTACTGCGCCTGGGGGTTG A C TSPAN4 Ensembl:ENSG00000214063 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:842851..843055;chr11:842851..843053 26863196 MeRIP-seq:(Medium) rs932436961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751893,Human_RBP_ID_4183894 Human_Splice_Rec_1196097,Human_Splice_Rec_1196111,Human_Splice_Rec_1196125 57871 RMVar_ID_57871 Human_SNP_ID_453065749 m1A Human chr11 - 844560 844560 844560 CTTGCCTGAGGAGGGCCAGGCCCAGGCTCCCCAGGGTCCTCAGGTAGAGCCCAGTCGGGACTGAG CTTGCCTGAGGAGGGCCAGGCCCAGGCTCCCCTGGGTCCTCAGGTAGAGCCCAGTCGGGACTGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:844555..849978 26863196 MeRIP-seq:(Medium) rs959604736 Functional Loss SNV dbSNP153 33..33 33 - - - 57872 RMVar_ID_57872 Human_SNP_ID_453065750 m1A Human chr11 - 844560 844560 844560 CTTGCCTGAGGAGGGCCAGGCCCAGGCTCCCCAGGGTCCTCAGGTAGAGCCCAGTCGGGACTGAG CTTGCCTGAGGAGGGCCAGGCCCAGGCTCCCCGGGGTCCTCAGGTAGAGCCCAGTCGGGACTGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:844555..849978 26863196 MeRIP-seq:(Medium) rs959604736 Functional Loss SNV dbSNP153 33..33 33 - - - 57873 RMVar_ID_57873 Human_SNP_ID_453065835 m1A Human chr11 + 844724 844724 844724 CTCGGCCTGGCTTCTGGGGGGGGGGGTCTGGGATGGGGCCAGGAGGGTGAGGCGCTGGTTTTATA CTCGGCCTGGCTTCTGGGGGGGGGGGTCTGGGGTGGGGCCAGGAGGGTGAGGCGCTGGTTTTATA A G TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:844721..844914 26863196 MeRIP-seq:(Medium) rs1226126843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2834,Human_RBP_ID_8173923,Human_RBP_ID_8725274,Human_RBP_ID_18456271 57874 RMVar_ID_57874 Human_SNP_ID_453065839 m1A Human chr11 + 844732 844732 844732 GGCTTCTGGGGGGGGGGGTCTGGGATGGGGCCAGGAGGGTGAGGCGCTGGTTTTATAGAAGGGGG GGCTTCTGGGGGGGGGGGTCTGGGATGGGGCCGGGAGGGTGAGGCGCTGGTTTTATAGAAGGGGG A G TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:844728..844914 26863196 MeRIP-seq:(Medium) rs1322881525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2834,Human_RBP_ID_259584,Human_RBP_ID_3383826,Human_RBP_ID_5643550,Human_RBP_ID_8173923,Human_RBP_ID_8725274,Human_RBP_ID_18456271,Human_RBP_ID_18932107,Human_RBP_ID_27836266 57875 RMVar_ID_57875 Human_SNP_ID_453066141 m1A Human chr11 + 845634 845634 845634 TGGGATGGCACCTGAGGTGCGGCTGCTCCTGGAGCCTGGGGGGTGTGGGAAGGTGCCCCCCACCC TGGGATGGCACCTGAGGTGCGGCTGCTCCTGGGGCCTGGGGGGTGTGGGAAGGTGCCCCCCACCC A G TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:845631..845701 26863196 MeRIP-seq:(Medium) rs1038206943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3383828,Human_RBP_ID_5126136,Human_RBP_ID_5313489,Human_RBP_ID_8063086,Human_RBP_ID_8173929,Human_RBP_ID_8725154,Human_RBP_ID_9415202,Human_RBP_ID_18456272,Human_RBP_ID_22709343 57876 RMVar_ID_57876 Human_SNP_ID_453067349 m1A Human chr11 - 849671 849671 849671 CAATCGCAGCCCCCGGCAACGCACCAGCCGCGACCCCGGCCCCTTCGCCCGCGCCGGCGCCCCAG CAATCGCAGCCCCCGGCAACGCACCAGCCGCGGCCCCGGCCCCTTCGCCCGCGCCGGCGCCCCAG T C lnc-POLR2L-3 RNACentral:URS0000D5A04C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:849660..849765 26863196 MeRIP-seq:(Medium) rs1344504043 Functional Loss SNV dbSNP153 33..33 33 - - - 57877 RMVar_ID_57877 Human_SNP_ID_453067470 m1A Human chr11 + 849856 849856 849856 GGGGCGCGGGGGCCGCAGCGCGCGGGCCGGGCAGATGTTTGGGTTCCGCCGCCGGGGTCCGAGCG GGGGCGCGGGGGCCGCAGCGCGCGGGCCGGGCGGATGTTTGGGTTCCGCCGCCGGGGTCCGAGCG A G TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:849843..850033;chr11:849852..850024 26863196 MeRIP-seq:(Medium) rs1024556573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259591,Human_RBP_ID_3384714,Human_RBP_ID_5167674,Human_RBP_ID_5313968,Human_RBP_ID_8173943,Human_RBP_ID_9415203,Human_RBP_ID_18456286,Human_RBP_ID_19050832,Human_RBP_ID_22414425,Human_RBP_ID_22570438,Human_RBP_ID_22695167,Human_RBP_ID_22709352,Human_RBP_ID_26755038 RMVar_hsa_circ_296316,RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_147489,RMVar_hsa_circ_147490 57878 RMVar_ID_57878 Human_SNP_ID_453067701 m1A Human chr11 + 850341 850341 850341 CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCATGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCGTGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT A G TSPAN4 Ensembl:ENSG00000214063 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:850276..850375 26863196 MeRIP-seq:(Medium) rs763642214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184578 Human_Splice_Rec_1196098,Human_Splice_Rec_1196099,Human_Splice_Rec_1196128,Human_Splice_Rec_1196129,Human_Splice_Rec_1196144,Human_Splice_Rec_1196145,Human_Splice_Rec_1196160,Human_Splice_Rec_1196161,Human_Splice_Rec_1196176,Human_Splice_Rec_1196177,Human_Splice_Rec_1196190,Human_Splice_Rec_1196191,Human_Splice_Rec_1196218,Human_Splice_Rec_1196219,Human_Splice_Rec_1196232,Human_Splice_Rec_1196233,Human_Splice_Rec_1196236,Human_Splice_Rec_1196237,Human_Splice_Rec_1196240,Human_Splice_Rec_1196241,Human_Splice_Rec_1196250,Human_Splice_Rec_1196251,Human_Splice_Rec_1196262,Human_Splice_Rec_1196263,Human_Splice_Rec_1196270,Human_Splice_Rec_1196271,Human_Splice_Rec_1196283 RMVar_hsa_circ_296316,RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_114660,RMVar_hsa_circ_147489,RMVar_hsa_circ_147490,RMVar_hsa_circ_147491 57879 RMVar_ID_57879 Human_SNP_ID_453067702 m1A Human chr11 + 850341 850341 850341 CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCATGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCTTGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT A T TSPAN4 Ensembl:ENSG00000214063 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:850276..850375 26863196 MeRIP-seq:(Medium) rs763642214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184578 Human_Splice_Rec_1196098,Human_Splice_Rec_1196099,Human_Splice_Rec_1196128,Human_Splice_Rec_1196129,Human_Splice_Rec_1196144,Human_Splice_Rec_1196145,Human_Splice_Rec_1196160,Human_Splice_Rec_1196161,Human_Splice_Rec_1196176,Human_Splice_Rec_1196177,Human_Splice_Rec_1196190,Human_Splice_Rec_1196191,Human_Splice_Rec_1196218,Human_Splice_Rec_1196219,Human_Splice_Rec_1196232,Human_Splice_Rec_1196233,Human_Splice_Rec_1196236,Human_Splice_Rec_1196237,Human_Splice_Rec_1196240,Human_Splice_Rec_1196241,Human_Splice_Rec_1196250,Human_Splice_Rec_1196251,Human_Splice_Rec_1196262,Human_Splice_Rec_1196263,Human_Splice_Rec_1196270,Human_Splice_Rec_1196271,Human_Splice_Rec_1196283 RMVar_hsa_circ_296316,RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_114660,RMVar_hsa_circ_147489,RMVar_hsa_circ_147490,RMVar_hsa_circ_147491 57880 RMVar_ID_57880 Human_SNP_ID_453069376 m1A Human chr11 - 855214 855214 855214 CCCTGGGCTGCCAATGCCACATCTCTGCCCCCAGAGACAGCCCTCTCCACACAGAGGCCCGGCCT CCCTGGGCTGCCAATGCCACATCTCTGCCCCCGGAGACAGCCCTCTCCACACAGAGGCCCGGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:855211..855368 26863196 MeRIP-seq:(Medium) rs28608948 Functional Loss SNV dbSNP153 33..33 33 - - - 57881 RMVar_ID_57881 Human_SNP_ID_453069936 m1A Human chr11 - 856996 856994 856996 CACAGACGCCTCACACCATCACACGTGGCCACACGCGCGCGTTACCGCCCTGCAACCTGGCGTCC CACAGACGCCTCACACCATCACACGTGGCCAC__GCGCGCGTTACCGCCCTGCAACCTGGCGTCC CGT C AP006623.1 Ensembl:ENSG00000250397 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:856994..857157 26863196 MeRIP-seq:(Medium) rs757286120 Functional Loss DEL dbSNP153 33..34 33 - - - 57882 RMVar_ID_57882 Human_SNP_ID_453070532 m1A Human chr11 - 858653 858653 858653 GGGAGCCTGGGGTGCGTGGGAACTGGGTGAGCAGGGTGTGTGAGCGGGGTGCGTGTGGGCCGGAG GGGAGCCTGGGGTGCGTGGGAACTGGGTGAGCGGGGTGTGTGAGCGGGGTGCGTGTGGGCCGGAG T C AP006623.1 Ensembl:ENSG00000250397 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:858476..858792 26863196 MeRIP-seq:(Medium) rs556990820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3386060,Human_RBP_ID_5313969,Human_RBP_ID_5643554,Human_RBP_ID_21965109,Human_RBP_ID_22471376 Human_Splice_Rec_1196316 57883 RMVar_ID_57883 Human_SNP_ID_453070789 m1A Human chr11 + 859162 859147 859163 GCACCCCTGGGCTCACATGCACCCCGGCTCACACGCACCCCAGGTCACACGCATCCCCTCACATG GCACCCCTGGGCTCACAT________________GCACCCCAGGTCACACGCATCCCCTCACATG TGCACCCCGGCTCACAC T TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:859007..859201 26863196 MeRIP-seq:(Medium) rs1307636919 Functional Loss DEL dbSNP153 19..34 33 - - - RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_147490 57884 RMVar_ID_57884 Human_SNP_ID_453070856 m1A Human chr11 + 859261 859261 859261 TCATCCCCGCTCACACACACCCCCACTCACACACACCCTGGCCCACACGCACCTTGGCTCACGTG TCATCCCCGCTCACACACACCCCCACTCACACGCACCCTGGCCCACACGCACCTTGGCTCACGTG A G TSPAN4 Ensembl:ENSG00000214063 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:859253..859437 26863196 MeRIP-seq:(Medium) rs1484706654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193249,Human_RBP_ID_24529619 RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_147490 57885 RMVar_ID_57885 Human_SNP_ID_453070863 m1A Human chr11 - 859267 859267 859267 GGGGTGCACGTGAGCCAAGGTGCGTGTGGGCCAGGGTGTGTGTGAGTGGGGGTGTGTGTGAGCGG GGGGTGCACGTGAGCCAAGGTGCGTGTGGGCCGGGGTGTGTGTGAGTGGGGGTGTGTGTGAGCGG T C AP006623.1 Ensembl:ENSG00000250397 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:859266..859396 26863196 MeRIP-seq:(Medium) rs1373989907 Functional Loss SNV dbSNP153 33..33 33 - - - 57886 RMVar_ID_57886 Human_SNP_ID_453070864 m1A Human chr11 - 859267 859267 859267 GGGGTGCACGTGAGCCAAGGTGCGTGTGGGCCAGGGTGTGTGTGAGTGGGGGTGTGTGTGAGCGG GGGGTGCACGTGAGCCAAGGTGCGTGTGGGCCCGGGTGTGTGTGAGTGGGGGTGTGTGTGAGCGG T G AP006623.1 Ensembl:ENSG00000250397 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:859266..859396 26863196 MeRIP-seq:(Medium) rs1373989907 Functional Loss SNV dbSNP153 33..33 33 - - - 57887 RMVar_ID_57887 Human_SNP_ID_453071103 m1A Human chr11 - 859520 859488 859521 GCCGGAGTGCATGTGGGCCCGGGGTGCGTGTAAGAGGGGGTGCGTGTGAGCCCGGGGTGCGTGTG GCCGGAGTGCATGTGGGCCCGGGGTGCGTGT_________________________________G CACACGCACCCCGGGCTCACACGCACCCCCTCTT C AP006623.1 Ensembl:ENSG00000250397 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:859423..859621 26863196 MeRIP-seq:(Medium) rs1293892965 Functional Loss DEL dbSNP153 32..64 33 - - - Human_RBP_ID_5643560,Human_RBP_ID_8174893,Human_RBP_ID_21965911,Human_RBP_ID_22471083 57888 RMVar_ID_57888 Human_SNP_ID_453071117 m1A Human chr11 - 859520 859505 859521 GCCGGAGTGCATGTGGGCCCGGGGTGCGTGTAAGAGGGGGTGCGTGTGAGCCCGGGGTGCGTGTG GCCGGAGTGCATGTGGGCCCGGGGTGCGTGT________________GAGCCCGGGGTGCGTGTG CACACGCACCCCCTCTT C AP006623.1 Ensembl:ENSG00000250397 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:859423..859621 26863196 MeRIP-seq:(Medium) rs1240140489 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_5643560,Human_RBP_ID_8174893,Human_RBP_ID_21965911,Human_RBP_ID_22471083 57889 RMVar_ID_57889 Human_SNP_ID_453071130 m1A Human chr11 - 859520 859519 859521 GCCGGAGTGCATGTGGGCCCGGGGTGCGTGTAAGAGGGGGTGCGTGTGAGCCCGGGGTGCGTGTG GCCGGAGTGCATGTGGGCCCGGGGTGCGTGT__GAGGGGGTGCGTGTGAGCCCGGGGTGCGTGTG CTT C AP006623.1 Ensembl:ENSG00000250397 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:859423..859621 26863196 MeRIP-seq:(Medium) rs1467455972 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5643560,Human_RBP_ID_8174893,Human_RBP_ID_21965911,Human_RBP_ID_22471083 57890 RMVar_ID_57890 Human_SNP_ID_453071152 m1A Human chr11 - 859565 859565 859565 TGGGGTGCGTGTGGGCCCGGGGTGCATGAGTGAGGGTGTGTGTGAGCCGGAGTGCATGTGGGCCC TGGGGTGCGTGTGGGCCCGGGGTGCATGAGTGGGGGTGTGTGTGAGCCGGAGTGCATGTGGGCCC T C AP006623.1 Ensembl:ENSG00000250397 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:859300..859710 26863196 MeRIP-seq:(Medium) rs1161121389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5643560,Human_RBP_ID_8174893,Human_RBP_ID_21965120,Human_RBP_ID_22471538,Human_RBP_ID_23524940 Human_Splice_Rec_1196315 57891 RMVar_ID_57891 Human_SNP_ID_453072195 m1A Human chr11 - 862569 862569 862569 CCTGTGTGGCGGCCAGCCAGATGCCGACACCCAGCACGCCACAGCCTCCCAGCTGGGGCACAGCA CCTGTGTGGCGGCCAGCCAGATGCCGACACCCGGCACGCCACAGCCTCCCAGCTGGGGCACAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:850276..862571 32194978 MeRIP-seq:(Medium) rs764537270 Functional Loss SNV dbSNP153 33..33 33 - - - 57892 RMVar_ID_57892 Human_SNP_ID_453072289 m1A Human chr11 + 862719 862719 862719 CGGCTTCGTGGGCTGCCTGGGTGCCATCAAGGAGAACAAGTGCCTCCTGCTCACTGTGAGTGCCG CGGCTTCGTGGGCTGCCTGGGTGCCATCAAGGTGAACAAGTGCCTCCTGCTCACTGTGAGTGCCG A T TSPAN4 Ensembl:ENSG00000214063 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:862669..862820 32194978 MeRIP-seq:(Medium) rs754028773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1196101,Human_Splice_Rec_1196115,Human_Splice_Rec_1196131,Human_Splice_Rec_1196147,Human_Splice_Rec_1196167,Human_Splice_Rec_1196179,Human_Splice_Rec_1196193,Human_Splice_Rec_1196207,Human_Splice_Rec_1196221,Human_Splice_Rec_1196253,Human_Splice_Rec_1196273,Human_Splice_Rec_1196285,Human_Splice_Rec_1196303 Human_miRNA_ID_2475524,Human_miRNA_ID_2961309 RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_147490 57893 RMVar_ID_57893 Human_SNP_ID_453074089 m1A Human chr11 + 867063 867063 867063 GCGGGGCCGTGGACCCCTCACCTACATTCCATAGTGGGCCCGTGGGGCTCCTGGTGCATCTTAAT GCGGGGCCGTGGACCCCTCACCTACATTCCATGGTGGGCCCGTGGGGCTCCTGGTGCATCTTAAT A G TSPAN4 Ensembl:ENSG00000214063 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:866666..867066 32194978 MeRIP-seq:(Medium) rs1211572819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_405466,Human_RBP_ID_5235353,Human_RBP_ID_8360660 RMVar_hsa_circ_101274,RMVar_hsa_circ_147492,RMVar_hsa_circ_95874,RMVar_hsa_circ_147493 57894 RMVar_ID_57894 Human_SNP_ID_453074630 m1A Human chr11 + 868612 868612 868612 GCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGAGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGA GCAGCTCGCAGGCCTCCCTGACGTCCAGGCGGGGGCTTTCTCAAGTGTGGGTGCCTTGGGTCCGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:868576..868956 26863196 MeRIP-seq:(Medium) rs1019445994 Functional Loss SNV dbSNP153 33..33 33 - - - 57895 RMVar_ID_57895 Human_SNP_ID_453074667 m1A Human chr11 + 868747 868747 868747 ATGTCCTGACCCCCTGCCCACTGCGCCCTAACATTACTGACTCTAAACCAGAACCCAGTGCCCAC ATGTCCTGACCCCCTGCCCACTGCGCCCTAACCTTACTGACTCTAAACCAGAACCCAGTGCCCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:868485..868978 26863196 MeRIP-seq:(Medium) rs972381841 Functional Loss SNV dbSNP153 33..33 33 - - - 57896 RMVar_ID_57896 Human_SNP_ID_453075304 m1A Human chr11 - 870423 870423 870423 ACAGCCAGGCCTCAGAGCACTTCTTCGAGTACAAGAAGTGAGTGTTTTGAAGTGCGTGGCCCACC ACAGCCAGGCCTCAGAGCACTTCTTCGAGTACCAGAAGTGAGTGTTTTGAAGTGCGTGGCCCACC T G CHID1 Ensembl:ENSG00000177830 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:869604..870423 32194978 MeRIP-seq:(Medium) rs761206835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1196336,Human_Splice_Rec_1196337,Human_Splice_Rec_1196360,Human_Splice_Rec_1196361,Human_Splice_Rec_1196384,Human_Splice_Rec_1196385,Human_Splice_Rec_1196389,Human_Splice_Rec_1196398,Human_Splice_Rec_1196399,Human_Splice_Rec_1196406,Human_Splice_Rec_1196407,Human_Splice_Rec_1196430,Human_Splice_Rec_1196431,Human_Splice_Rec_1196456,Human_Splice_Rec_1196457,Human_Splice_Rec_1196480,Human_Splice_Rec_1196481,Human_Splice_Rec_1196485,Human_Splice_Rec_1196492,Human_Splice_Rec_1196493,Human_Splice_Rec_1196510 RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_116638,RMVar_hsa_circ_147494,RMVar_hsa_circ_147495,RMVar_hsa_circ_147496 57897 RMVar_ID_57897 Human_SNP_ID_453077380 m1A Human chr11 + 877709 877709 877709 TGTTCTCTGCAAAATTCACACTGAAATGTAATACCCACTGTGGCACTGTGGGGAGGCGGGGCCTT TGTTCTCTGCAAAATTCACACTGAAATGTAATGCCCACTGTGGCACTGTGGGGAGGCGGGGCCTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:877684..877921 26863196 MeRIP-seq:(Medium) rs934634857 Functional Loss SNV dbSNP153 33..33 33 - - - 57898 RMVar_ID_57898 Human_SNP_ID_453079366 m1A Human chr11 - 884168 884168 884168 AGCCTGAGGTGGCTGCACCTGTCTGTTACAGGACCGACCAGCTGGGCATGTTCACGCACAAGGAG AGCCTGAGGTGGCTGCACCTGTCTGTTACAGGTCCGACCAGCTGGGCATGTTCACGCACAAGGAG T A CHID1 Ensembl:ENSG00000177830 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:884134..899361 32194978 MeRIP-seq:(Medium) rs1420444013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867057,Human_RBP_ID_11775888,Human_RBP_ID_26803112 Human_Splice_Rec_1196332,Human_Splice_Rec_1196356,Human_Splice_Rec_1196380,Human_Splice_Rec_1196426,Human_Splice_Rec_1196452,Human_Splice_Rec_1196476,Human_Splice_Rec_1196522,Human_Splice_Rec_1196536,Human_Splice_Rec_1196552 RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_116638,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147495,RMVar_hsa_circ_147496,RMVar_hsa_circ_294866,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_273307,RMVar_hsa_circ_147498,RMVar_hsa_circ_147499,RMVar_hsa_circ_147497 57899 RMVar_ID_57899 Human_SNP_ID_453079741 m1A Human chr11 + 885474 885473 885474 CAGGTACGTGGAGCATCATCCATGGTCCCCTCAGCCCCGACCTCTTTTCCTGATGCCTGCCAGCC CAGGTACGTGGAGCATCATCCATGGTCCCCTC_GCCCCGACCTCTTTTCCTGATGCCTGCCAGCC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:885469..885622 26863196 MeRIP-seq:(Medium) rs150274830 Functional Loss DEL dbSNP153 33..33 33 - - - 57900 RMVar_ID_57900 Human_SNP_ID_453080681 m1A Human chr11 + 888719 888719 888719 ACCCTCCCATCGCCATGTCGTGGGTGGGCCCCATGCAGGCAGCGGCATGCAAGTTGAGTGCCCAC ACCCTCCCATCGCCATGTCGTGGGTGGGCCCCGTGCAGGCAGCGGCATGCAAGTTGAGTGCCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:888714..889108 26863196 MeRIP-seq:(Medium) rs1327291968 Functional Loss SNV dbSNP153 33..33 33 - - - 57901 RMVar_ID_57901 Human_SNP_ID_453080786 m1A Human chr11 - 888991 888991 888991 CAGAGCGGCCTGTCTCAGCACAAAGCCTGAGCAGGGGCAGCCCGGGAAGAGCAGAGCGCGTCCAG CAGAGCGGCCTGTCTCAGCACAAAGCCTGAGCGGGGGCAGCCCGGGAAGAGCAGAGCGCGTCCAG T C CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:888985..889589 26863196 MeRIP-seq:(Medium) rs1003891242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_116638,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147495,RMVar_hsa_circ_147496,RMVar_hsa_circ_294866,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_147498,RMVar_hsa_circ_147499 57902 RMVar_ID_57902 Human_SNP_ID_453080978 m1A Human chr11 - 889810 889810 889810 CAGATGCCCTGAGCATGGGAGATTGCAGGGACAGTGATGCCAGCATCTGTTAGGGTTGGGGAAAG CAGATGCCCTGAGCATGGGAGATTGCAGGGACGGTGATGCCAGCATCTGTTAGGGTTGGGGAAAG T C CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:889807..889891 26863196 MeRIP-seq:(Medium) rs1439227621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11742887 RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_116638,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147495,RMVar_hsa_circ_147496,RMVar_hsa_circ_294866,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_147498,RMVar_hsa_circ_147499 57903 RMVar_ID_57903 Human_SNP_ID_453082841 m1A Human chr11 - 895862 895862 895862 GCTGCAGGAAGGTCGGGAGCTGCCAGCATGGCAGGGGCAGGCAGTATCCAGGCTCCTCAGAGCAG GCTGCAGGAAGGTCGGGAGCTGCCAGCATGGCCGGGGCAGGCAGTATCCAGGCTCCTCAGAGCAG T G CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:895854..896207;chr11:895853..896212 26863196 MeRIP-seq:(Medium) rs924857374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2369,Human_RBP_ID_259609,Human_RBP_ID_3383843,Human_RBP_ID_5138475,Human_RBP_ID_8063173,Human_RBP_ID_8174010,Human_RBP_ID_8725304,Human_RBP_ID_9414423,Human_RBP_ID_17350451,Human_RBP_ID_18159167,Human_RBP_ID_18477466,Human_RBP_ID_18932130,Human_RBP_ID_22414428,Human_RBP_ID_22736321,Human_RBP_ID_24550908 RMVar_hsa_circ_57161,RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147496,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_147499,RMVar_hsa_circ_365575,RMVar_hsa_circ_359857 57904 RMVar_ID_57904 Human_SNP_ID_453083020 m1A Human chr11 + 896298 896295 896298 GTCTCAGCACCCCCAGCCTCCACCCCAGACACAACGAGGCTGTCTCAGTGCCCCCAGCCTCCACC GTCTCAGCACCCCCAGCCTCCACCCCAGAC___ACGAGGCTGTCTCAGTGCCCCCAGCCTCCACC CACA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:896296..896495 26863196 MeRIP-seq:(Medium) rs552034363 Functional Loss DEL dbSNP153 31..33 33 - - - 57905 RMVar_ID_57905 Human_SNP_ID_453083303 m1A Human chr11 + 896953 896951 896953 GAGCCTGTCTCAGCACCCCCAGCCTCCACCCCAGACACAACGAGCCTGTCTCAGCACCCCCAGCC GAGCCTGTCTCAGCACCCCCAGCCTCCACCC__GACACAACGAGCCTGTCTCAGCACCCCCAGCC CCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:896951..897179 26863196 MeRIP-seq:(Medium) rs1298111033 Functional Loss DEL dbSNP153 32..33 33 - - - 57906 RMVar_ID_57906 Human_SNP_ID_453083335 m1A Human chr11 - 897024 897024 897024 AGGTGCTGAGACAGGCTCGTTGTGTCGGGTGGAGGCTGGGGGTGCTGAGACAGGCTCGTGTCTGG AGGTGCTGAGACAGGCTCGTTGTGTCGGGTGGGGGCTGGGGGTGCTGAGACAGGCTCGTGTCTGG T C CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:896735..897153 26863196 MeRIP-seq:(Medium) rs1487228196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259613,Human_RBP_ID_8174018,Human_RBP_ID_17110788 RMVar_hsa_circ_57161,RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147496,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_147499,RMVar_hsa_circ_365575,RMVar_hsa_circ_359857 57907 RMVar_ID_57907 Human_SNP_ID_453083336 m1A Human chr11 - 897024 897024 897024 AGGTGCTGAGACAGGCTCGTTGTGTCGGGTGGAGGCTGGGGGTGCTGAGACAGGCTCGTGTCTGG AGGTGCTGAGACAGGCTCGTTGTGTCGGGTGGCGGCTGGGGGTGCTGAGACAGGCTCGTGTCTGG T G CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:896735..897153 26863196 MeRIP-seq:(Medium) rs1487228196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259613,Human_RBP_ID_8174018,Human_RBP_ID_17110788 RMVar_hsa_circ_57161,RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_147494,RMVar_hsa_circ_113988,RMVar_hsa_circ_147496,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_147499,RMVar_hsa_circ_365575,RMVar_hsa_circ_359857 57908 RMVar_ID_57908 Human_SNP_ID_453085782 m1A Human chr11 - 904816 904816 904816 CCGAGGTTGGACCCTACTGTGACACACCTACCATGCGGACACTCTTCAACCTCCTCTGGCTTGCC CCGAGGTTGGACCCTACTGTGACACACCTACCGTGCGGACACTCTTCAACCTCCTCTGGCTTGCC T C CHID1 Ensembl:ENSG00000177830 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:904776..904850 26863196 MeRIP-seq:(Medium) rs958359935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184579,Human_RBP_ID_5110696,Human_RBP_ID_8361193,Human_RBP_ID_9321220,Human_RBP_ID_11744740,Human_RBP_ID_22640810,Human_RBP_ID_26803115,Human_RBP_ID_26898745,Human_RBP_ID_27416846 Human_Splice_Rec_1196318,Human_Splice_Rec_1196366,Human_Splice_Rec_1196414,Human_Splice_Rec_1196436,Human_Splice_Rec_1196568,Human_Splice_Rec_1196580,Human_Splice_Rec_1196588,Human_Splice_Rec_1196592,Human_Splice_Rec_1196594 RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_365575,RMVar_hsa_circ_359857,RMVar_hsa_circ_359756,RMVar_hsa_circ_375919,RMVar_hsa_circ_147500 57909 RMVar_ID_57909 Human_SNP_ID_453097321 m1A Human chr11 - 943998 943998 943998 CCGGTCGGGACTCTCTTACTCTCGCCATCTCCACTGCCACCTGCATCTCCGGTCGGACTCTCCTA CCGGTCGGGACTCTCTTACTCTCGCCATCTCCGCTGCCACCTGCATCTCCGGTCGGACTCTCCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:943995..944147 26863196 MeRIP-seq:(Medium) rs1268535647 Functional Loss SNV dbSNP153 33..33 33 - - - 57910 RMVar_ID_57910 Human_SNP_ID_453097481 m1A Human chr11 + 944596 944593 944597 GGTGAGATGTTAGAAGATGATAAACACAACAGAGAGATATTAAGGGGGGAAGGTGATTGGGTAAA GGTGAGATGTTAGAAGATGATAAACACAAC____AGATATTAAGGGGGGAAGGTGATTGGGTAAA CAGAG C AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:944594..945267 26863196 MeRIP-seq:(Medium) rs1460821617 Functional Loss DEL dbSNP153 31..34 33 - - - 57911 RMVar_ID_57911 Human_SNP_ID_453097761 m1A Human chr11 + 945821 945821 945821 AAAAATAAGAACAGAAAAGGAAAAGAATGGTCATTTTGGATATAGAGGATGGGTTTTAGGTGAGG AAAAATAAGAACAGAAAAGGAAAAGAATGGTCGTTTTGGATATAGAGGATGGGTTTTAGGTGAGG A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:945818..945970 26863196 MeRIP-seq:(Medium) rs1321741054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9653001,Human_RBP_ID_11754501 57912 RMVar_ID_57912 Human_SNP_ID_453101964 m1A Human chr11 + 961119 961119 961119 CAGAAGCAGATGGAGATGTGGGTCTGACAGTCACCACCACCAGTGAAAAGTAAAGGGCAGAAGCA CAGAAGCAGATGGAGATGTGGGTCTGACAGTCGCCACCACCAGTGAAAAGTAAAGGGCAGAAGCA A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:961115..961348 26863196 MeRIP-seq:(Medium) rs954206783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292644 57913 RMVar_ID_57913 Human_SNP_ID_453102060 m1A Human chr11 + 961406 961406 961406 AAGCAGATGGAGATGTGGGTCTGACAGTCGCCACCACTAGTGAAAAGTAAAGGGCAGAAGCAGAT AAGCAGATGGAGATGTGGGTCTGACAGTCGCCGCCACTAGTGAAAAGTAAAGGGCAGAAGCAGAT A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:961403..961851 26863196 MeRIP-seq:(Medium) rs28418982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292644 57914 RMVar_ID_57914 Human_SNP_ID_453103053 m1A Human chr11 + 964867 964811 964867 TAAAGGAAATAATCCCAGATGGAAGCGTGGAGATGGAAAGCATGGAACGGGCGGGAAATTAAAGG _________________________________TGGAAAGCATGGAACGGGCGGGAAATTAAAGG GAAAGCATGGAACGGGCAGGAAATTAAAGGAAATAATCCCAGATGGAAGCGTGGAGA G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:964807..964908;chr11:964816..964933 26863196 MeRIP-seq:(Medium) rs1564796916 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_292644 57915 RMVar_ID_57915 Human_SNP_ID_453103070 m1A Human chr11 + 964867 964867 964867 TAAAGGAAATAATCCCAGATGGAAGCGTGGAGATGGAAAGCATGGAACGGGCGGGAAATTAAAGG TAAAGGAAATAATCCCAGATGGAAGCGTGGAGGTGGAAAGCATGGAACGGGCGGGAAATTAAAGG A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:964807..964908;chr11:964816..964933 26863196 MeRIP-seq:(Medium) rs7396338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292644 57916 RMVar_ID_57916 Human_SNP_ID_453103102 m1A Human chr11 + 965251 965251 965251 AGGTGGAAAGCATGGAACGGGCGGGAAATTAAAGGAAATAATCCCAGATGGAAGCGTGGAGGTGG AGGTGGAAAGCATGGAACGGGCGGGAAATTAAGGGAAATAATCCCAGATGGAAGCGTGGAGGTGG A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:965244..965391 26863196 MeRIP-seq:(Medium) rs1476385895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8229161 RMVar_hsa_circ_292644 57917 RMVar_ID_57917 Human_SNP_ID_453104773 m1A Human chr11 - 971166 971166 971166 TCTCCCCCAGGACAAGGGCAGGCCCAAGTTCCAGTCCCTGTGCCTCCGTCCTCAAGGCTAATCCC TCTCCCCCAGGACAAGGGCAGGCCCAAGTTCCGGTCCCTGTGCCTCCGTCCTCAAGGCTAATCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:971153..971478 26863196 MeRIP-seq:(Medium) rs7103585 Functional Loss SNV dbSNP153 33..33 33 - - - 57918 RMVar_ID_57918 Human_SNP_ID_453105087 m1A Human chr11 - 972210 972210 972210 CCTTAGGGATCTCCCCGGCGAAGGCCTCGGCCATCTCCCGGCTGCCCACGCTGGCGATGCAGTGC CCTTAGGGATCTCCCCGGCGAAGGCCTCGGCCGTCTCCCGGCTGCCCACGCTGGCGATGCAGTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:972159..977099 32194978 MeRIP-seq:(Medium) rs1331833868 Functional Loss SNV dbSNP153 33..33 33 - - - 57919 RMVar_ID_57919 Human_SNP_ID_453109710 m1A Human chr11 + 986943 986943 986943 GGCTGTCAAGACGCACATCGAGACGGTCATCAACGCCCTGAAGGCGAGTGCCCTGTCCTTGGGTT GGCTGTCAAGACGCACATCGAGACGGTCATCAGCGCCCTGAAGGCGAGTGCCCTGTCCTTGGGTT A G AP2A2 Ensembl:ENSG00000183020 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:986741..986975 26863196 MeRIP-seq:(Medium) rs1390646128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864737,Human_RBP_ID_9363291,Human_RBP_ID_18410465,Human_RBP_ID_19048972,Human_RBP_ID_26320783 Human_miRNA_ID_2353575,Human_miRNA_ID_2353576 RMVar_hsa_circ_8883,RMVar_hsa_circ_268660,RMVar_hsa_circ_365699,RMVar_hsa_circ_286563,RMVar_hsa_circ_79421,RMVar_hsa_circ_147505,RMVar_hsa_circ_147506,RMVar_hsa_circ_373656,RMVar_hsa_circ_127009,RMVar_hsa_circ_103735,RMVar_hsa_circ_147508,RMVar_hsa_circ_376464,RMVar_hsa_circ_147509,RMVar_hsa_circ_147510 57920 RMVar_ID_57920 Human_SNP_ID_453117303 m1A Human chr11 - 1010997 1010996 1010998 CCCACGCCATGCACAGTGGCACTGCTGCTCCCAGAGGCTCCGAGGCGGGGTGGGCGGCAGCACGG CCCACGCCATGCACAGTGGCACTGCTGCTCC__GAGGCTCCGAGGCGGGGTGGGCGGCAGCACGG CTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1010946..1011047 32194978 MeRIP-seq:(Medium) rs746658104 Functional Loss DEL dbSNP153 32..33 33 - - - 57921 RMVar_ID_57921 Human_SNP_ID_453119146 m1A Human chr11 + 1016166 1016166 1016166 AGAGGGTGAAAGGAGAGGAGATAGTGTGGGGGAGAGTGGCCCTAATGGTAGTAGAGGCAGCTGGA AGAGGGTGAAAGGAGAGGAGATAGTGTGGGGGCGAGTGGCCCTAATGGTAGTAGAGGCAGCTGGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1016157..1016322 26863196 MeRIP-seq:(Medium) rs764190393 Functional Loss SNV dbSNP153 33..33 33 - - - 57922 RMVar_ID_57922 Human_SNP_ID_453119231 m1A Human chr11 + 1016302 1016302 1016302 CGAGCTCAGGGTTGTGGAGTGCACGGGGGCGGACACGAAAGAGGAAGATGTGCCAACAGAAGGCG CGAGCTCAGGGTTGTGGAGTGCACGGGGGCGGCCACGAAAGAGGAAGATGTGCCAACAGAAGGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1013979..1016395 26863196 MeRIP-seq:(Medium) rs959890350 Functional Loss SNV dbSNP153 33..33 33 - - - 57923 RMVar_ID_57923 Human_SNP_ID_453119662 m1A Human chr11 + 1016852 1016852 1016852 GTAGTGGTGGTCTGGAAGGATGTTGCAGTCATAGGACCTGTGGAAGAGAAGGGACTGCTCCCTGT GTAGTGGTGGTCTGGAAGGATGTTGCAGTCATGGGACCTGTGGAAGAGAAGGGACTGCTCCCTGT A G NONHSAG007366.2,NONHSAG007366.2:2,NONHSAG007366.2:3 RNACentral:URS00008B9B31,RNACentral:URS00008B4D59,RNACentral:URS00008B8EE5 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:1016587..1018548;chr11:1016487..1017600;chr11:1016587..1018233 26863196 MeRIP-seq:(Medium) rs1471162158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11502551,Human_RBP_ID_23482534,Human_RBP_ID_27613636 57924 RMVar_ID_57924 Human_SNP_ID_453119697 m1A Human chr11 + 1016885 1016885 1016885 GGACCTGTGGAAGAGAAGGGACTGCTCCCTGTAGGTGGGGAGTGTGTGGTGAAGGGTGTGGGTAG GGACCTGTGGAAGAGAAGGGACTGCTCCCTGTCGGTGGGGAGTGTGTGGTGAAGGGTGTGGGTAG A C NONHSAG007366.2,NONHSAG007366.2:2,NONHSAG007366.2:3 RNACentral:URS00008B9B31,RNACentral:URS00008B4D59,RNACentral:URS00008B8EE5 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1016836..1017037 26863196 MeRIP-seq:(Medium) rs760998763 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23482539 57925 RMVar_ID_57925 Human_SNP_ID_453120636 m1A Human chr11 + 1017724 1017724 1017724 ATGGTGTGTGGAGGAAGTGTGTGAATGTAGGGATGTAGAGGTTTTGGCTGTGTTTAATGAGCTCA ATGGTGTGTGGAGGAAGTGTGTGAATGTAGGGTTGTAGAGGTTTTGGCTGTGTTTAATGAGCTCA A T NONHSAG007366.2,NONHSAG007366.2:2,NONHSAG007366.2:3 RNACentral:URS00008B9B31,RNACentral:URS00008BF6F5,RNACentral:URS00008B8EE5 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1017685..1018533 26863196 MeRIP-seq:(Medium) rs748691294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11502634,Human_RBP_ID_23482563 57926 RMVar_ID_57926 Human_SNP_ID_453120647 m1A Human chr11 - 1017735 1017735 1017735 CAGCCAAGCCCTGAGCTCATTAAACACAGCCAAAACCTCTACATCCCTACATTCACACACTTCCT CAGCCAAGCCCTGAGCTCATTAAACACAGCCACAACCTCTACATCCCTACATTCACACACTTCCT T G MUC6 Ensembl:ENSG00000184956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1017684..1017835 26863196 MeRIP-seq:(Medium) rs1309107982 Functional Loss SNV dbSNP153 33..33 33 - - - 57927 RMVar_ID_57927 Human_SNP_ID_453122146 m1A Human chr11 + 1020183 1020183 1020183 GGGGCTGGCAGGGGTGTGATTAGAGCTGGGTGAGGGTCCGGTGGAGCTGAGAAGCCCGATGGTGG GGGGCTGGCAGGGGTGTGATTAGAGCTGGGTGGGGGTCCGGTGGAGCTGAGAAGCCCGATGGTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1020150..1020291 26863196 MeRIP-seq:(Medium) rs1466635619 Functional Loss SNV dbSNP153 33..33 33 - - - 57928 RMVar_ID_57928 Human_SNP_ID_453215435 m1A Human chr11 + 1287702 1287702 1287702 CCGCACCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCTGCACCCTCTCTGCCGCAGCCT CCGCACCCTCCCCGCCGCAGCCTCCCCGCCGCGGCCTCCCCGCTGCACCCTCTCTGCCGCAGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1287692..1287939 26863196 MeRIP-seq:(Medium) rs1420162691 Functional Loss SNV dbSNP153 33..33 33 - - - 57929 RMVar_ID_57929 Human_SNP_ID_453215436 m1A Human chr11 + 1287702 1287702 1287702 CCGCACCCTCCCCGCCGCAGCCTCCCCGCCGCAGCCTCCCCGCTGCACCCTCTCTGCCGCAGCCT CCGCACCCTCCCCGCCGCAGCCTCCCCGCCGCTGCCTCCCCGCTGCACCCTCTCTGCCGCAGCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1287692..1287939 26863196 MeRIP-seq:(Medium) rs1420162691 Functional Loss SNV dbSNP153 33..33 33 - - - 57930 RMVar_ID_57930 Human_SNP_ID_453216896 m1A Human chr11 + 1291558 1291554 1291558 CCACCCCCCGAAGGCACGGCCACCCCATCCTCACTGACGCCCCTCTGAGGGCACGGCCACCCTGT CCACCCCCCGAAGGCACGGCCACCCCATC____CTGACGCCCCTCTGAGGGCACGGCCACCCTGT CCTCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1291556..1291945 26863196 MeRIP-seq:(Medium) rs1203532779 Functional Loss DEL dbSNP153 30..33 33 - - - 57931 RMVar_ID_57931 Human_SNP_ID_453220930 m1A Human chr11 + 1305931 1305921 1305931 GCAGAAGGCAGGGGTCCACACGGTACTCCTCGATACTCCTCGCGGGGGCCCGCACGGTACCCCTC GCAGAAGGCAGGGGTCCACACGG__________TACTCCTCGCGGGGGCCCGCACGGTACCCCTC GTACTCCTCGA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1305925..1306029 32194978 MeRIP-seq:(Medium) rs1564981950 Functional Loss DEL dbSNP153 24..33 33 - - - 57932 RMVar_ID_57932 Human_SNP_ID_453221349 m1A Human chr11 + 1307331 1307331 1307331 TGGAAACAGCCCAGGAGGCACTGGGCAAGAGGAGATTCTAACGACACCTCAGCACTTGCCAGCAC TGGAAACAGCCCAGGAGGCACTGGGCAAGAGGCGATTCTAACGACACCTCAGCACTTGCCAGCAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1307325..1307425 32194978 MeRIP-seq:(Medium) rs1261183526 Functional Loss SNV dbSNP153 33..33 33 - - - 57933 RMVar_ID_57933 Human_SNP_ID_453228429 m1A Human chr11 - 1336508 1336508 1336508 GACGGTTTCCCTGACGGATGCGCTTCCGGGGGAGAAGTGAGGGGGGCACGGGGCGGTACTGGGGG GACGGTTTCCCTGACGGATGCGCTTCCGGGGGGGAAGTGAGGGGGGCACGGGGCGGTACTGGGGG T C AC136297.1 Ensembl:ENSG00000287935 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1336471..1336628 26863196 MeRIP-seq:(Medium) rs1310953651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1197345 57934 RMVar_ID_57934 Human_SNP_ID_453228458 m1A Human chr11 + 1336626 1336626 1336626 ATTCAGACGCGAAGACAAAGCGTCCCTGGCTCAGCCCTGAGAAGCAGCGGGACGGCGGCGCGTTC ATTCAGACGCGAAGACAAAGCGTCCCTGGCTCTGCCCTGAGAAGCAGCGGGACGGCGGCGCGTTC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:1336613..1336745 26863196 MeRIP-seq:(Medium) rs1425370711 Functional Loss SNV dbSNP153 33..33 33 - - - 57935 RMVar_ID_57935 Human_SNP_ID_453233282 m1A Human chr11 - 1351734 1351734 1351734 AGGCAGAGGGTTTAATCCACCCACCTCGCAAGAGTGTCAGGAACAACAGGTCATTTCTCAAAGGC AGGCAGAGGGTTTAATCCACCCACCTCGCAAGCGTGTCAGGAACAACAGGTCATTTCTCAAAGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:1351720..1351915 26863196 MeRIP-seq:(Medium) rs1014568600 Functional Loss SNV dbSNP153 33..33 33 - - - 57936 RMVar_ID_57936 Human_SNP_ID_453233362 m1A Human chr11 + 1351793 1351793 1351793 CTGCCTCTGCTAGCTTTTCTCCCAGGTCTCACACCTGGACCCCCCACCCCCACCAACTCCCCTCC CTGCCTCTGCTAGCTTTTCTCCCAGGTCTCACCCCTGGACCCCCCACCCCCACCAACTCCCCTCC A C LINC02689 Ensembl:ENSG00000285985 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1351752..1351969 26863196 MeRIP-seq:(Medium) rs1186671499 Functional Loss SNV dbSNP153 33..33 33 - - - 57937 RMVar_ID_57937 Human_SNP_ID_453233363 m1A Human chr11 + 1351793 1351793 1351793 CTGCCTCTGCTAGCTTTTCTCCCAGGTCTCACACCTGGACCCCCCACCCCCACCAACTCCCCTCC CTGCCTCTGCTAGCTTTTCTCCCAGGTCTCACGCCTGGACCCCCCACCCCCACCAACTCCCCTCC A G LINC02689 Ensembl:ENSG00000285985 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1351752..1351969 26863196 MeRIP-seq:(Medium) rs1186671499 Functional Loss SNV dbSNP153 33..33 33 - - - 57938 RMVar_ID_57938 Human_SNP_ID_453233785 m1A Human chr11 + 1352702 1352702 1352702 CCACCAACTTCCATCCCAGGCCTCACACCTGGACCCCCACCCCCACCAACTCCCCTCCCAGGCCT CCACCAACTTCCATCCCAGGCCTCACACCTGGCCCCCCACCCCCACCAACTCCCCTCCCAGGCCT A C LINC02689 Ensembl:ENSG00000285985 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1352694..1352809 26863196 MeRIP-seq:(Medium) rs1336772729 Functional Loss SNV dbSNP153 33..33 33 - - - 57939 RMVar_ID_57939 Human_SNP_ID_453242703 m1A Human chr11 - 1383146 1383146 1383146 GGACAAGCTCACGGCCACCAGGAGCTGGGCCGAGGGCCCGTGGGGGGAGGGCAGGTGGCACGGGT GGACAAGCTCACGGCCACCAGGAGCTGGGCCGGGGGCCCGTGGGGGGAGGGCAGGTGGCACGGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1383139..1383321 26863196 MeRIP-seq:(Medium) rs956599352 Functional Loss SNV dbSNP153 33..33 33 - - - 57940 RMVar_ID_57940 Human_SNP_ID_453244694 m1A Human chr11 - 1390224 1390213 1390224 CGCCCGGGCGCGCGGGCAGGGAGGGGCCGCCCAGCGTCCGCCCGCGTCCGCCGAGTGCCGTCCGC CGCCCGGGCGCGCGGGCAGGGAGGGGCCGCCC___________GCGTCCGCCGAGTGCCGTCCGC CGGGCGGACGCT C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:1390146..1390247 26863410 MeRIP-seq:(Medium) rs1167553357 Functional Loss DEL dbSNP153 33..43 33 - - - 57941 RMVar_ID_57941 Human_SNP_ID_453245206 m1A Human chr11 + 1391615 1391615 1391615 CCACGGCACGGAAGGGCCCCTGGCCACAGGGCAGGACCTGGGCAGGTGGGGTGGTGCAGCCTGGG CCACGGCACGGAAGGGCCCCTGGCCACAGGGCGGGACCTGGGCAGGTGGGGTGGTGCAGCCTGGG A G BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1391609..1391746 32194978 MeRIP-seq:(Medium) rs1306931159 Functional Loss SNV dbSNP153 33..33 33 - - - 57942 RMVar_ID_57942 Human_SNP_ID_453258384 m1A Human chr11 - 1435974 1435974 1435974 CCAGGGTGCCTGCAGCGAGCACCCAGCCGGACAGTGCAGGTTGGGGGCCTCCTCCCACGTCCTGG CCAGGGTGCCTGCAGCGAGCACCCAGCCGGACGGTGCAGGTTGGGGGCCTCCTCCCACGTCCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1435970..1436057 26863196 MeRIP-seq:(Medium) rs988316987 Functional Loss SNV dbSNP153 33..33 33 - - - 57943 RMVar_ID_57943 Human_SNP_ID_453258730 m1A Human chr11 + 1436912 1436912 1436912 GGGAGGCTTGTGGAAGGTGCTAAGGGTTGGGGACTGTGACATGTTGGGCACCCCCCAGCTGCTGG GGGAGGCTTGTGGAAGGTGCTAAGGGTTGGGGTCTGTGACATGTTGGGCACCCCCCAGCTGCTGG A T BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1436906..1437035 26863196 MeRIP-seq:(Medium) rs895707866 Functional Loss SNV dbSNP153 33..33 33 - - - 57944 RMVar_ID_57944 Human_SNP_ID_453265601 m1A Human chr11 + 1454191 1454176 1454191 GGGGGGCTCACCTGTGGGGGGCTCACCTGTGGAGGGGCATCCCCAGACTTGGGAGTGGGTGGCAT GGGGGGCTCACCTGTGGG_______________GGGGCATCCCCAGACTTGGGAGTGGGTGGCAT GGGGCTCACCTGTGGA G BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1454140..1454248 26863196 MeRIP-seq:(Medium) rs140446560 Functional Loss DEL dbSNP153 19..33 33 - - - RMVar_hsa_circ_266764 57945 RMVar_ID_57945 Human_SNP_ID_453265616 m1A Human chr11 + 1454191 1454190 1454191 GGGGGGCTCACCTGTGGGGGGCTCACCTGTGGAGGGGCATCCCCAGACTTGGGAGTGGGTGGCAT GGGGGGCTCACCTGTGGGGGGCTCACCTGTGG_GGGGCATCCCCAGACTTGGGAGTGGGTGGCAT GA G BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1454140..1454248 26863196 MeRIP-seq:(Medium) rs148190768 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_266764 57946 RMVar_ID_57946 Human_SNP_ID_453265620 m1A Human chr11 + 1454191 1454191 1454191 GGGGGGCTCACCTGTGGGGGGCTCACCTGTGGAGGGGCATCCCCAGACTTGGGAGTGGGTGGCAT GGGGGGCTCACCTGTGGGGGGCTCACCTGTGGGGGGGCATCCCCAGACTTGGGAGTGGGTGGCAT A G BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1454140..1454248 26863196 MeRIP-seq:(Medium) rs74233938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266764 57947 RMVar_ID_57947 Human_SNP_ID_453267696 m1A Human chr11 - 1459238 1459236 1459239 GAGGTGCCAGGTGAGCGTGGGGGATTCTTACCACATTTGGAAAGCCGCCCCGTCATCATTTCCAT GAGGTGCCAGGTGAGCGTGGGGGATTCTTAC___ATTTGGAAAGCCGCCCCGTCATCATTTCCAT TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1459221..1459379 26863196 MeRIP-seq:(Medium) rs768483881 Functional Loss DEL dbSNP153 32..34 33 - - - 57948 RMVar_ID_57948 Human_SNP_ID_453267720 m1A Human chr11 + 1459259 1459254 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCAC_____CCTGGCACCTCCACCTGCCACTTCACCGCTCA CGCTCA C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs752162907 Functional Loss DEL dbSNP153 29..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57949 RMVar_ID_57949 Human_SNP_ID_453267726 m1A Human chr11 + 1459259 1459256 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCACGC___CCTGGCACCTCCACCTGCCACTTCACCGCTCA CTCA C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs781719064 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57950 RMVar_ID_57950 Human_SNP_ID_453267730 m1A Human chr11 + 1459259 1459258 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCACGCTC_CCTGGCACCTCCACCTGCCACTTCACCGCTCA CA C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs756426132 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57951 RMVar_ID_57951 Human_SNP_ID_453267734 m1A Human chr11 + 1459259 1459259 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCACGCTCCCCTGGCACCTCCACCTGCCACTTCACCGCTCA A C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs768100269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57952 RMVar_ID_57952 Human_SNP_ID_453267735 m1A Human chr11 + 1459259 1459259 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCACGCTCGCCTGGCACCTCCACCTGCCACTTCACCGCTCA A G BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs768100269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57953 RMVar_ID_57953 Human_SNP_ID_453267736 m1A Human chr11 + 1459259 1459259 1459259 CTTTCCAAATGTGGTAAGAATCCCCCACGCTCACCTGGCACCTCCACCTGCCACTTCACCGCTCA CTTTCCAAATGTGGTAAGAATCCCCCACGCTCTCCTGGCACCTCCACCTGCCACTTCACCGCTCA A T BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1459256..1459333 26863196 MeRIP-seq:(Medium) rs768100269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1197390,Human_Splice_Rec_1197430,Human_Splice_Rec_1197506,Human_Splice_Rec_1197640,Human_Splice_Rec_1197672,Human_Splice_Rec_1197696,Human_Splice_Rec_1197708,Human_Splice_Rec_1197718,Human_Splice_Rec_1197726 57954 RMVar_ID_57954 Human_SNP_ID_453268769 m1A Human chr11 - 1461120 1461120 1461120 CTTCCTCCCACGGGCCGTGCGGAGCTGAGGCGAGGAGCTGCCGCGGGGTGGACGGGGCGCTGGGC CTTCCTCCCACGGGCCGTGCGGAGCTGAGGCGGGGAGCTGCCGCGGGGTGGACGGGGCGCTGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1460943..1461403 26863196 MeRIP-seq:(Medium) rs139099614 Functional Loss SNV dbSNP153 33..33 33 - - - 57955 RMVar_ID_57955 Human_SNP_ID_453268912 m1A Human chr11 - 1461396 1461396 1461396 TGAGGCAAGGGAGGCGCGGGTGAGACGAGAGGACGGGAGGCAGCCTGAGGAGGCCAAGACTACAC TGAGGCAAGGGAGGCGCGGGTGAGACGAGAGGGCGGGAGGCAGCCTGAGGAGGCCAAGACTACAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1461347..1461497 32194978 MeRIP-seq:(Medium) rs1029525612 Functional Loss SNV dbSNP153 33..33 33 - - - 57956 RMVar_ID_57956 Human_SNP_ID_453272562 m1A Human chr11 + 1471803 1471803 1471803 CTGTTTTTCTGTTGTATTTTGAAAGCACACAGAGGCTCCTTCTCTTCCCAGGAAGCTGTGCTGTG CTGTTTTTCTGTTGTATTTTGAAAGCACACAGTGGCTCCTTCTCTTCCCAGGAAGCTGTGCTGTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1471799..1471899 32194978 MeRIP-seq:(Medium) rs1218843740 Functional Loss SNV dbSNP153 33..33 33 - - - 57957 RMVar_ID_57957 Human_SNP_ID_453278366 m1A Human chr11 + 1491534 1491531 1491535 ATACATATAACACAGGCGGAGACACACAACACAGACAAAGACACACAACACAGACGAAGATATAC ATACATATAACACAGGCGGAGACACACAAC____ACAAAGACACACAACACAGACGAAGATATAC CACAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1491483..1491575 26863196 MeRIP-seq:(Medium) rs930818131 Functional Loss DEL dbSNP153 31..34 33 - - - 57958 RMVar_ID_57958 Human_SNP_ID_453278741 m1A Human chr11 + 1492800 1492800 1492800 AGACCTGGCAGAGAACAGCTCTGGGAAGCGTGAGGAAGAGAGGTTCTGGAGGCCACACGGGGCAG AGACCTGGCAGAGAACAGCTCTGGGAAGCGTGGGGAAGAGAGGTTCTGGAGGCCACACGGGGCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:1492662..1492845 26863196 MeRIP-seq:(Medium) rs1393762902 Functional Loss SNV dbSNP153 33..33 33 - - - 57959 RMVar_ID_57959 Human_SNP_ID_453285652 m1A Human chr11 - 1517571 1517571 1517571 GGGTAGCGGTGACAACAGGAAGAGCTGGTGCGAGAGAGAAGGAGCTGGAAGGAGCTGTGACGGGT GGGTAGCGGTGACAACAGGAAGAGCTGGTGCGTGAGAGAAGGAGCTGGAAGGAGCTGTGACGGGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1517520..1517774 26863196 MeRIP-seq:(Medium) rs542150348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57960 RMVar_ID_57960 Human_SNP_ID_453297187 m1A Human chr11 - 1557289 1557289 1557289 CCCGCGCCCCCCACGCCCCCGGCGACCAGCGCACTGCAGCAGGGCCTGCGCGGCCTGCACCTCTC CCCGCGCCCCCCACGCCCCCGGCGACCAGCGCGCTGCAGCAGGGCCTGCGCGGCCTGCACCTCTC T C DUSP8 Ensembl:ENSG00000184545 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1557240..1557414 32194978 MeRIP-seq:(Medium) rs1330456460 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57961 RMVar_ID_57961 Human_SNP_ID_453297188 m1A Human chr11 - 1557289 1557289 1557289 CCCGCGCCCCCCACGCCCCCGGCGACCAGCGCACTGCAGCAGGGCCTGCGCGGCCTGCACCTCTC CCCGCGCCCCCCACGCCCCCGGCGACCAGCGCCCTGCAGCAGGGCCTGCGCGGCCTGCACCTCTC T G DUSP8 Ensembl:ENSG00000184545 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:1557240..1557414 32194978 MeRIP-seq:(Medium) rs1330456460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57962 RMVar_ID_57962 Human_SNP_ID_453297537 m1A Human chr11 - 1558152 1558152 1558152 ATGCGGGTCCCCATCAACGACAACTACTGTGAAAAACTGCTGCCCTGGCTGGACAAGTCCATCGA ATGCGGGTCCCCATCAACGACAACTACTGTGATAAACTGCTGCCCTGGCTGGACAAGTCCATCGA T A DUSP8 Ensembl:ENSG00000184545 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1558088..1558155 26863196 MeRIP-seq:(Medium) rs775764872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1197765,Human_Splice_Rec_1197777,Human_Splice_Rec_1197785 RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57963 RMVar_ID_57963 Human_SNP_ID_453301602 m1A Human chr11 + 1571854 1571854 1571854 GGCGCCCTCCGCCCCCCGGCCCGGGCCGGTGAACCCCATCCCCGGCGCCCGCCCCCGCCCCGCCG GGCGCCCTCCGCCCCCCGGCCCGGGCCGGTGACCCCCATCCCCGGCGCCCGCCCCCGCCCCGCCG A C KRTAP5-AS1 Ensembl:ENSG00000233930 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:1571847..1571985 26863410 MeRIP-seq:(Medium) rs1032797993 Functional Loss SNV dbSNP153 33..33 33 - - - 57964 RMVar_ID_57964 Human_SNP_ID_453302300 m1A Human chr11 - 1573758 1573758 1573758 CCCTCCCGCTTTGGGGCGCAGCCCCAACCCCAATAACCCCTGGGCTCCCTTCCGGGACAGACCCA CCCTCCCGCTTTGGGGCGCAGCCCCAACCCCAGTAACCCCTGGGCTCCCTTCCGGGACAGACCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1573707..1574013 26863196 MeRIP-seq:(Medium) rs1001913461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57965 RMVar_ID_57965 Human_SNP_ID_453305455 m1A Human chr11 - 1584034 1584034 1584034 GCAGTCACTAGGAGTTCAGATCTCTGTCCTTTAAACATCCAATAAACCGCTCACCCCAGCACCCC GCAGTCACTAGGAGTTCAGATCTCTGTCCTTTCAACATCCAATAAACCGCTCACCCCAGCACCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1584028..1584654 26863196 MeRIP-seq:(Medium) rs145441789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57966 RMVar_ID_57966 Human_SNP_ID_453305677 m1A Human chr11 - 1584670 1584661 1584670 GCAAGGGGGGCTGCGGTTCTTGTGGGGGATCCAAGGGGGGTTGTGGCTCCGGCTGTGGGGGCTGT GCAAGGGGGGCTGCGGTTCTTGTGGGGGATCC_________TGTGGCTCCGGCTGTGGGGGCTGT AACCCCCCTT A KRTAP5-1 Ensembl:ENSG00000205869 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:1584627..1584749 26863196 MeRIP-seq:(Medium) rs1346346599 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 57967 RMVar_ID_57967 Human_SNP_ID_453355110 m1A Human chr11 + 1747803 1747803 1747803 GGTAGACCTCGATGACGGTCGTGGGGTTGGTCATCGTCTTCTTCTCGGCTAGGTGCTTGCAGGCA GGTAGACCTCGATGACGGTCGTGGGGTTGGTCGTCGTCTTCTTCTCGGCTAGGTGCTTGCAGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1747787..1747937 26863196 MeRIP-seq:(Medium) rs983475095 Functional Loss SNV dbSNP153 33..33 33 - - - 57968 RMVar_ID_57968 Human_SNP_ID_453356796 m1A Human chr11 - 1753004 1753004 1753004 CACCCTACCTGTTCAGTGTCCCGGGCCCGTTGAGGATGAGGCCGCTAGAGGCCTGAGGATGAGCT CACCCTACCTGTTCAGTGTCCCGGGCCCGTTGGGGATGAGGCCGCTAGAGGCCTGAGGATGAGCT T C AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1752851..1753558 26863196 MeRIP-seq:(Medium) rs1235006019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393233,Human_RBP_ID_748763,Human_RBP_ID_5110698,Human_RBP_ID_5138477,Human_RBP_ID_8176165,Human_RBP_ID_17648931,Human_RBP_ID_17793265,Human_RBP_ID_23497247,Human_RBP_ID_26402744 Human_miRNA_ID_1968564,Human_miRNA_ID_3122086 RMVar_hsa_circ_108626,RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_114255,RMVar_hsa_circ_119606,RMVar_hsa_circ_109547,RMVar_hsa_circ_147536,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_89570,RMVar_hsa_circ_147539,RMVar_hsa_circ_147537,RMVar_hsa_circ_147534,RMVar_hsa_circ_147535,RMVar_hsa_circ_147533 57969 RMVar_ID_57969 Human_SNP_ID_453358684 m1A Human chr11 - 1757427 1757427 1757427 TCATCGCAGCCAAGTTCGATGGCATCCTGGGCATGGCCTACCCCCGCATCTCCGTCAACAACGTG TCATCGCAGCCAAGTTCGATGGCATCCTGGGCCTGGCCTACCCCCGCATCTCCGTCAACAACGTG T G AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1757376..1757505 26863196 MeRIP-seq:(Medium) rs1281616300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870526,Human_RBP_ID_9001716,Human_RBP_ID_18468890,Human_RBP_ID_22433376,Human_RBP_ID_22753275,Human_RBP_ID_26803117,Human_RBP_ID_27410551 RMVar_hsa_circ_108626,RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_119606,RMVar_hsa_circ_84171,RMVar_hsa_circ_147536,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_147539,RMVar_hsa_circ_147537,RMVar_hsa_circ_351490,RMVar_hsa_circ_25793,RMVar_hsa_circ_43374,RMVar_hsa_circ_147541,RMVar_hsa_circ_147542,RMVar_hsa_circ_59744 57970 RMVar_ID_57970 Human_SNP_ID_453359201 m1A Human chr11 - 1759085 1759085 1759085 ACCGGCGGGCCCCCTTGTCGCCCGGGGCAGGGATCCACCACAAGTACAACAGCGACAAGTCCAGC ACCGGCGGGCCCCCTTGTCGCCCGGGGCAGGGTTCCACCACAAGTACAACAGCGACAAGTCCAGC T A AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1759076..1759100 26863196 MeRIP-seq:(Medium) rs768013885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8063966,Human_RBP_ID_19048984,Human_RBP_ID_22642722,Human_RBP_ID_22753280,Human_RBP_ID_26803118 Human_Splice_Rec_1197836,Human_Splice_Rec_1197856,Human_Splice_Rec_1197884,Human_Splice_Rec_1197900,Human_Splice_Rec_1197914,Human_Splice_Rec_1197936,Human_Splice_Rec_1197952,Human_Splice_Rec_1197978,Human_Splice_Rec_1197994,Human_Splice_Rec_1198016,Human_Splice_Rec_1198028,Human_Splice_Rec_1198036 Human_miRNA_ID_2477584 RMVar_hsa_circ_108626,RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_84171,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_147539,RMVar_hsa_circ_147537,RMVar_hsa_circ_351490,RMVar_hsa_circ_25793,RMVar_hsa_circ_43374,RMVar_hsa_circ_147541,RMVar_hsa_circ_147542,RMVar_hsa_circ_59744,RMVar_hsa_circ_69425,RMVar_hsa_circ_112280,RMVar_hsa_circ_147543 57971 RMVar_ID_57971 Human_SNP_ID_453359202 m1A Human chr11 - 1759085 1759085 1759085 ACCGGCGGGCCCCCTTGTCGCCCGGGGCAGGGATCCACCACAAGTACAACAGCGACAAGTCCAGC ACCGGCGGGCCCCCTTGTCGCCCGGGGCAGGGGTCCACCACAAGTACAACAGCGACAAGTCCAGC T C AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1759076..1759100 26863196 MeRIP-seq:(Medium) rs768013885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8063966,Human_RBP_ID_19048984,Human_RBP_ID_22642722,Human_RBP_ID_22753280,Human_RBP_ID_26803118 Human_Splice_Rec_1197836,Human_Splice_Rec_1197856,Human_Splice_Rec_1197884,Human_Splice_Rec_1197900,Human_Splice_Rec_1197914,Human_Splice_Rec_1197936,Human_Splice_Rec_1197952,Human_Splice_Rec_1197978,Human_Splice_Rec_1197994,Human_Splice_Rec_1198016,Human_Splice_Rec_1198028,Human_Splice_Rec_1198036 Human_miRNA_ID_2477584 RMVar_hsa_circ_108626,RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_84171,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_147539,RMVar_hsa_circ_147537,RMVar_hsa_circ_351490,RMVar_hsa_circ_25793,RMVar_hsa_circ_43374,RMVar_hsa_circ_147541,RMVar_hsa_circ_147542,RMVar_hsa_circ_59744,RMVar_hsa_circ_69425,RMVar_hsa_circ_112280,RMVar_hsa_circ_147543 57972 RMVar_ID_57972 Human_SNP_ID_453359349 m1A Human chr11 - 1759504 1759504 1759504 AACTGCTGGACATCGCTTGCTGTGAGTCACGAACCCTGGCCCCGTCGCCCAGGTCCTGCCCTTCC AACTGCTGGACATCGCTTGCTGTGAGTCACGACCCCTGGCCCCGTCGCCCAGGTCCTGCCCTTCC T G AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1759501..1759550 26863196 MeRIP-seq:(Medium) rs765749835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108768,Human_RBP_ID_864743,Human_RBP_ID_19048985 RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_84171,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_147539,RMVar_hsa_circ_351490,RMVar_hsa_circ_25793,RMVar_hsa_circ_43374,RMVar_hsa_circ_147541,RMVar_hsa_circ_147542,RMVar_hsa_circ_59744,RMVar_hsa_circ_69425,RMVar_hsa_circ_112280,RMVar_hsa_circ_147543 57973 RMVar_ID_57973 Human_SNP_ID_453359378 m1A Human chr11 - 1759576 1759576 1759576 CGCCCCCCCAGTGCTTCACAGTCGTCTTCGACACGGGCTCCTCCAACCTGTGGGTCCCCTCCATC CGCCCCCCCAGTGCTTCACAGTCGTCTTCGACTCGGGCTCCTCCAACCTGTGGGTCCCCTCCATC T A AC068580.4,CTSD Ensembl:ENSG00000250644,Ensembl:ENSG00000117984 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:1759526..1761375 32194978 MeRIP-seq:(Medium) rs11555042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108768,Human_RBP_ID_5139203,Human_RBP_ID_17348088,Human_RBP_ID_22753281,Human_RBP_ID_27410556,Human_RBP_ID_27836505 Human_Splice_Rec_1197834,Human_Splice_Rec_1197835,Human_Splice_Rec_1197854,Human_Splice_Rec_1197855,Human_Splice_Rec_1197882,Human_Splice_Rec_1197883,Human_Splice_Rec_1197898,Human_Splice_Rec_1197899,Human_Splice_Rec_1197912,Human_Splice_Rec_1197913,Human_Splice_Rec_1197934,Human_Splice_Rec_1197935,Human_Splice_Rec_1197950,Human_Splice_Rec_1197951,Human_Splice_Rec_1197976,Human_Splice_Rec_1197977,Human_Splice_Rec_1197992,Human_Splice_Rec_1197993,Human_Splice_Rec_1198014,Human_Splice_Rec_1198015,Human_Splice_Rec_1198026,Human_Splice_Rec_1198027,Human_Splice_Rec_1198034,Human_Splice_Rec_1198035 RMVar_hsa_circ_55625,RMVar_hsa_circ_127061,RMVar_hsa_circ_147530,RMVar_hsa_circ_104097,RMVar_hsa_circ_84171,RMVar_hsa_circ_99334,RMVar_hsa_circ_104765,RMVar_hsa_circ_147538,RMVar_hsa_circ_147540,RMVar_hsa_circ_147539,RMVar_hsa_circ_351490,RMVar_hsa_circ_25793,RMVar_hsa_circ_43374,RMVar_hsa_circ_147541,RMVar_hsa_circ_147542,RMVar_hsa_circ_59744,RMVar_hsa_circ_69425,RMVar_hsa_circ_112280,RMVar_hsa_circ_147543 57974 RMVar_ID_57974 Human_SNP_ID_453360394 m1A Human chr11 + 1762850 1762850 1762850 TTGGGGCTACCCGCCCCCGGGCCATTCCCCACAGCCTTTGGTGAGGCTCAGTCCTACCCAGCTGG TTGGGGCTACCCGCCCCCGGGCCATTCCCCACTGCCTTTGGTGAGGCTCAGTCCTACCCAGCTGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1762848..1762918 26863196 MeRIP-seq:(Medium) rs959907895 Functional Loss SNV dbSNP153 33..33 33 - - - 57975 RMVar_ID_57975 Human_SNP_ID_453360697 m1A Human chr11 + 1763842 1763839 1763842 GGTGCAGCCAGCAGGCAGAGGGCGAGCGGCAGAAGGCTGGAGGGCTGCATGGCGGCGGCGGCCGG GGTGCAGCCAGCAGGCAGAGGGCGAGCGGC___AGGCTGGAGGGCTGCATGGCGGCGGCGGCCGG CAGA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr11:1763809..1763907;chr11:1763804..1763954 26863410 MeRIP-seq:(Medium) rs1420082715 Functional Loss DEL dbSNP153 31..33 33 - - - 57976 RMVar_ID_57976 Human_SNP_ID_453360719 m1A Human chr11 + 1763882 1763872 1763882 AGGGCTGCATGGCGGCGGCGGCCGGGTCGGAGAGGGTCGCCGAGGCCGTGCGCTTATAGCCGGGA AGGGCTGCATGGCGGCGGCGGCC__________GGGTCGCCGAGGCCGTGCGCTTATAGCCGGGA CGGGTCGGAGA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:1763720..1763950 26863196 MeRIP-seq:(Medium) rs905220328 Functional Loss DEL dbSNP153 24..33 33 - - - 57977 RMVar_ID_57977 Human_SNP_ID_453417494 m1A Human chr11 - 1947374 1947374 1947374 GACGGGGGGGTGACGACCCCTACTCACACCACATTCCGCGCCATGGCGGCCACGCGCGCTTCCGG GACGGGGGGGTGACGACCCCTACTCACACCACTTTCCGCGCCATGGCGGCCACGCGCGCTTCCGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:1947351..1947451 26863410 MeRIP-seq:(Medium) rs773061135 Functional Loss SNV dbSNP153 33..33 33 - - - 57978 RMVar_ID_57978 Human_SNP_ID_453418257 m1A Human chr11 + 1950879 1950879 1950879 TCGGGCTGCCTTGGCCTAAGTGTGTGACATGGACCCAATCTCTTCTGTACAGGTACCCCCTGTAC TCGGGCTGCCTTGGCCTAAGTGTGTGACATGGGCCCAATCTCTTCTGTACAGGTACCCCCTGTAC A G MRPL23 Ensembl:ENSG00000214026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:1950876..1951064;chr11:1950876..1950950;chr11:1950876..1951025 26863196 MeRIP-seq:(Medium) rs200471692 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 57979 RMVar_ID_57979 Human_SNP_ID_453419716 m1A Human chr11 + 1956315 1956315 1956315 GATCTGTTTCCCGAGAAAGACGAGAGCCCTGAAGGCAGCGCTGCCGACGACCTCTACAGCATGCT GATCTGTTTCCCGAGAAAGACGAGAGCCCTGACGGCAGCGCTGCCGACGACCTCTACAGCATGCT A C MRPL23 Ensembl:ENSG00000214026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1956306..1956600 26863196 MeRIP-seq:(Medium) rs202115348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393580,Human_RBP_ID_1455687,Human_RBP_ID_3372476,Human_RBP_ID_9361895,Human_RBP_ID_17649431 Human_Splice_Rec_1198884,Human_Splice_Rec_1198894,Human_Splice_Rec_1198928,Human_Splice_Rec_1198938,Human_Splice_Rec_1198944 57980 RMVar_ID_57980 Human_SNP_ID_453426267 m1A Human chr11 - 1984846 1984846 1984846 CACCATCTCACTCTCCAAGTCCCTTCTCGGTGAGACGGGGGGCCTTGCACCCACCTCCCAGCCCC CACCATCTCACTCTCCAAGTCCCTTCTCGGTGGGACGGGGGGCCTTGCACCCACCTCCCAGCCCC T C MRPL23-AS1 Ensembl:ENSG00000226416 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1984839..1984925 26863196 MeRIP-seq:(Medium) rs373099173 Functional Loss SNV dbSNP153 33..33 33 - - - 57981 RMVar_ID_57981 Human_SNP_ID_453426816 m1A Human chr11 - 1987627 1987627 1987627 GGTCTAGAGCCTAGAAATGGACCCCCACGTCCACCTGCCCAGCCTAGACCCCCAGCATTGAAGGG GGTCTAGAGCCTAGAAATGGACCCCCACGTCCCCCTGCCCAGCCTAGACCCCCAGCATTGAAGGG T G MRPL23-AS1 Ensembl:ENSG00000226416 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1987625..1988012 26863196 MeRIP-seq:(Medium) rs926283574 Functional Loss SNV dbSNP153 33..33 33 - - - 57982 RMVar_ID_57982 Human_SNP_ID_453426836 m1A Human chr11 + 1987793 1987793 1987793 CCGCCCAGCCCAGCCCAGTCTGTCTGCTCCCCAGCCTCCCACGCCCCCCATTGGCGTGCATGAGT CCGCCCAGCCCAGCCCAGTCTGTCTGCTCCCCGGCCTCCCACGCCCCCCATTGGCGTGCATGAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1987785..1987990 26863196 MeRIP-seq:(Medium) rs899171656 Functional Loss SNV dbSNP153 33..33 33 - - - 57983 RMVar_ID_57983 Human_SNP_ID_453428603 m1A Human chr11 - 1995271 1995271 1995271 GAAGCTCCGACCGACATCACGGAGCAGCCTTCAAGCATTCCATTACGCCCCATCTCGCTCTGTGC GAAGCTCCGACCGACATCACGGAGCAGCCTTCCAGCATTCCATTACGCCCCATCTCGCTCTGTGC T G H19 Ensembl:ENSG00000130600 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:1995221..1995857 26863196 MeRIP-seq:(Medium) rs763768485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5549127 Human_miRNA_ID_2924325,Human_miRNA_ID_3204538 RMVar_hsa_circ_147550,RMVar_hsa_circ_99310,RMVar_hsa_circ_116698,RMVar_hsa_circ_147551 57984 RMVar_ID_57984 Human_SNP_ID_453428838 m1A Human chr11 - 1995739 1995739 1995739 CATCAGCCCAACATCAAAGACACCATCGGAACAGCAGCGCCCGCAGCACCCACCCCGCACCGGCG CATCAGCCCAACATCAAAGACACCATCGGAACGGCAGCGCCCGCAGCACCCACCCCGCACCGGCG T C H19 Ensembl:ENSG00000130600 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:1995205..1995879 26863196 MeRIP-seq:(Medium) rs746288770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5549132 Human_Splice_Rec_1198958,Human_Splice_Rec_1198962,Human_Splice_Rec_1198968,Human_Splice_Rec_1198982,Human_Splice_Rec_1198990,Human_Splice_Rec_1198998,Human_Splice_Rec_1199006,Human_Splice_Rec_1199012,Human_Splice_Rec_1199018 RMVar_hsa_circ_147550,RMVar_hsa_circ_99310,RMVar_hsa_circ_116698,RMVar_hsa_circ_147551 57985 RMVar_ID_57985 Human_SNP_ID_453429152 m1A Human chr11 - 1996392 1996382 1996393 CAGCCAGGTCTCCAGCTGGGGTGGACGTGCCCACCAGCTGCCGAAGGCCAAGACGCCAGGTCCGG CAGCCAGGTCTCCAGCTGGGGTGGACGTGCC___________GAAGGCCAAGACGCCAGGTCCGG CGGCAGCTGGTG C H19 Ensembl:ENSG00000130600 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:1995189..1997850 26863196 MeRIP-seq:(Medium) rs765022022 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_259373,Human_RBP_ID_5550886,Human_RBP_ID_18188149 Human_Splice_Rec_1198964,Human_Splice_Rec_1198970,Human_Splice_Rec_1198976,Human_Splice_Rec_1198984,Human_Splice_Rec_1198992,Human_Splice_Rec_1199000,Human_Splice_Rec_1199008 Human_miRNA_ID_2051666,Human_miRNA_ID_2873375,Human_miRNA_ID_2981338,Human_miRNA_ID_3152874,Human_miRNA_ID_3201540,Human_miRNA_ID_3207850 RMVar_hsa_circ_80311,RMVar_hsa_circ_147550,RMVar_hsa_circ_99310,RMVar_hsa_circ_116698,RMVar_hsa_circ_147551,RMVar_hsa_circ_128033,RMVar_hsa_circ_147554,RMVar_hsa_circ_147555 57986 RMVar_ID_57986 Human_SNP_ID_453429160 m1A Human chr11 - 1996389 1996389 1996389 CCAGGTCTCCAGCTGGGGTGGACGTGCCCACCAGCTGCCGAAGGCCAAGACGCCAGGTCCGGTGG CCAGGTCTCCAGCTGGGGTGGACGTGCCCACCGGCTGCCGAAGGCCAAGACGCCAGGTCCGGTGG T C H19 Ensembl:ENSG00000130600 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:1995972..1997850 26863196 MeRIP-seq:(Medium) rs1271841785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5549140,Human_RBP_ID_18188149 Human_Splice_Rec_1198964,Human_Splice_Rec_1198970,Human_Splice_Rec_1198976,Human_Splice_Rec_1198984,Human_Splice_Rec_1198992,Human_Splice_Rec_1199000,Human_Splice_Rec_1199008 Human_miRNA_ID_2051666,Human_miRNA_ID_2873375,Human_miRNA_ID_2981338,Human_miRNA_ID_3152874,Human_miRNA_ID_3201540,Human_miRNA_ID_3207850 RMVar_hsa_circ_80311,RMVar_hsa_circ_147550,RMVar_hsa_circ_99310,RMVar_hsa_circ_116698,RMVar_hsa_circ_147551,RMVar_hsa_circ_128033,RMVar_hsa_circ_147554,RMVar_hsa_circ_147555 57987 RMVar_ID_57987 Human_SNP_ID_453533172 m1A Human chr11 + 2377471 2377447 2377471 GCCCCTCGGCCCGCCAGGCCCCCTTGCCGGCCACCCGCCAGGCCCCGCGCCGGCCCGCCCGCCGC GCCCCTCGG________________________CCCGCCAGGCCCCGCGCCGGCCCGCCCGCCGC GCCCGCCAGGCCCCCTTGCCGGCCA G CD81 Ensembl:ENSG00000110651 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:2377301..2377562 26863196 MeRIP-seq:(Medium) rs1439903092 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_226415,Human_RBP_ID_4184593,Human_RBP_ID_9275395,Human_RBP_ID_9321239,Human_RBP_ID_22532261,Human_RBP_ID_22570465,Human_RBP_ID_26803120 Human_miRNA_ID_2250118,Human_miRNA_ID_3065886 RMVar_hsa_circ_115338,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562 57988 RMVar_ID_57988 Human_SNP_ID_453533180 m1A Human chr11 + 2377471 2377471 2377471 GCCCCTCGGCCCGCCAGGCCCCCTTGCCGGCCACCCGCCAGGCCCCGCGCCGGCCCGCCCGCCGC GCCCCTCGGCCCGCCAGGCCCCCTTGCCGGCCCCCCGCCAGGCCCCGCGCCGGCCCGCCCGCCGC A C CD81 Ensembl:ENSG00000110651 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:2377301..2377562 26863196 MeRIP-seq:(Medium) rs1322314341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226415,Human_RBP_ID_4184593,Human_RBP_ID_9275395,Human_RBP_ID_9321239,Human_RBP_ID_22532261,Human_RBP_ID_22570465,Human_RBP_ID_26803120 Human_miRNA_ID_2250118,Human_miRNA_ID_3065886 RMVar_hsa_circ_115338,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562 57989 RMVar_ID_57989 Human_SNP_ID_453533183 m1A Human chr11 + 2377478 2377478 2377478 GGCCCGCCAGGCCCCCTTGCCGGCCACCCGCCAGGCCCCGCGCCGGCCCGCCCGCCGCCCAGGAC GGCCCGCCAGGCCCCCTTGCCGGCCACCCGCCTGGCCCCGCGCCGGCCCGCCCGCCGCCCAGGAC A T CD81 Ensembl:ENSG00000110651 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:2377301..2377512 26863196 MeRIP-seq:(Medium) rs1251356919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226415,Human_RBP_ID_4184593,Human_RBP_ID_9275395,Human_RBP_ID_9321239,Human_RBP_ID_22532261,Human_RBP_ID_22570465 Human_miRNA_ID_2250118,Human_miRNA_ID_3065886 RMVar_hsa_circ_115338,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562 57990 RMVar_ID_57990 Human_SNP_ID_453533194 m1A Human chr11 + 2377526 2377498 2377527 CGCCCGCCGCCCAGGACCGGCCCGCGCCCCGCAGGCCGCCCGCCGCCCGCGCCGCCATGGGAGTG CGCCC_____________________________GCCGCCCGCCGCCCGCGCCGCCATGGGAGTG CGCCGCCCAGGACCGGCCCGCGCCCCGCAG C CD81 Ensembl:ENSG00000110651 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:2377476..2377670 26863196 MeRIP-seq:(Medium) rs1349396535 Functional Loss DEL dbSNP153 6..34 33 - - - Human_RBP_ID_29967,Human_RBP_ID_226415,Human_RBP_ID_4156881,Human_RBP_ID_9321239,Human_RBP_ID_22532261 Human_Splice_Rec_1199567 Human_miRNA_ID_2250120,Human_miRNA_ID_3065887 RMVar_hsa_circ_115338,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562 57991 RMVar_ID_57991 Human_SNP_ID_453533247 m1A Human chr11 - 2377613 2377607 2377613 TCCCGCCCCGGCCCCCGGCGCAGCCCTTACCCAGAAGACGAAATTGAAGACGAAGAGCAGGTACT TCCCGCCCCGGCCCCCGGCGCAGCCCTTACCC______CGAAATTGAAGACGAAGAGCAGGTACT GTCTTCT G CD81-AS1 Ensembl:ENSG00000238184 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2377312..2379202 32194978 MeRIP-seq:(Medium) rs1339099807 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_5550684 Human_Splice_Rec_1199537,Human_Splice_Rec_1199541 57992 RMVar_ID_57992 Human_SNP_ID_453533651 m1A Human chr11 - 2379026 2379026 2379026 CCTAGCTGCCCCCACTGCCAGGGCAGTGCCGAAGGCCACAGTGACTCCCACCAGCGTCCCAAGCA CCTAGCTGCCCCCACTGCCAGGGCAGTGCCGACGGCCACAGTGACTCCCACCAGCGTCCCAAGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2379022..2379219 26863196 MeRIP-seq:(Medium) rs1450435675 Functional Loss SNV dbSNP153 33..33 33 - - - 57993 RMVar_ID_57993 Human_SNP_ID_453534809 m1A Human chr11 - 2382888 2382888 2382888 AGCCCTACTCTAAGCCTCTAAGCCCTACTCTAAGCCCCTCGGAAACCCCTGGGGTCCCACTCGGG AGCCCTACTCTAAGCCTCTAAGCCCTACTCTAGGCCCCTCGGAAACCCCTGGGGTCCCACTCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2382882..2383036 32194978 MeRIP-seq:(Medium) rs1323913387 Functional Loss SNV dbSNP153 33..33 33 - - - 57994 RMVar_ID_57994 Human_SNP_ID_453537163 m1A Human chr11 + 2390464 2390464 2390464 GGGTGTGGCCCTGTGGCTCCGCCATGACCCGCAGACCACCAACCTCCTGTATCTGGAGCTGGGAG GGGTGTGGCCCTGTGGCTCCGCCATGACCCGCGGACCACCAACCTCCTGTATCTGGAGCTGGGAG A G CD81 Ensembl:ENSG00000110651 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:2390401..2390525 26863196 MeRIP-seq:(Medium) rs1438014764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393883,Human_RBP_ID_1264150,Human_RBP_ID_1354092,Human_RBP_ID_4156888,Human_RBP_ID_8348618,Human_RBP_ID_22432740,Human_RBP_ID_22753285,Human_RBP_ID_27200461 Human_Splice_Rec_1199548,Human_Splice_Rec_1199549,Human_Splice_Rec_1199560,Human_Splice_Rec_1199561,Human_Splice_Rec_1199568,Human_Splice_Rec_1199569,Human_Splice_Rec_1199581,Human_Splice_Rec_1199588,Human_Splice_Rec_1199589,Human_Splice_Rec_1199602,Human_Splice_Rec_1199603,Human_Splice_Rec_1199616,Human_Splice_Rec_1199617,Human_Splice_Rec_1199628,Human_Splice_Rec_1199629,Human_Splice_Rec_1199636,Human_Splice_Rec_1199637,Human_Splice_Rec_1199650,Human_Splice_Rec_1199651,Human_Splice_Rec_1199662,Human_Splice_Rec_1199663,Human_Splice_Rec_1199676,Human_Splice_Rec_1199677,Human_Splice_Rec_1199687 RMVar_hsa_circ_115338,RMVar_hsa_circ_109574,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562,RMVar_hsa_circ_147564 57995 RMVar_ID_57995 Human_SNP_ID_453537197 m1A Human chr11 + 2390549 2390549 2390549 TTCTATGTAGGTGAGTGCACATGTGGCCGCAGACGCATTCAGGGAGGGCTTCTAGGAGGAGGCAG TTCTATGTAGGTGAGTGCACATGTGGCCGCAGGCGCATTCAGGGAGGGCTTCTAGGAGGAGGCAG A G CD81 Ensembl:ENSG00000110651 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:2390545..2390663;chr11:2390544..2390659 26863196 MeRIP-seq:(Medium) rs770758666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115338,RMVar_hsa_circ_109574,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562,RMVar_hsa_circ_147564 57996 RMVar_ID_57996 Human_SNP_ID_453538730 m1A Human chr11 - 2395472 2395472 2395472 TTCACCACAGCCTTGGCGTTGTTGGCGTCATCATCCACCACGGCCTGCTGTAGGGCCTGGTCATA TTCACCACAGCCTTGGCGTTGTTGGCGTCATCGTCCACCACGGCCTGCTGTAGGGCCTGGTCATA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2395401..2395525 32194978 MeRIP-seq:(Medium) rs772886745 Functional Loss SNV dbSNP153 33..33 33 - - - 57997 RMVar_ID_57997 Human_SNP_ID_453538739 m1A Human chr11 + 2395485 2395485 2395485 TACAGCAGGCCGTGGTGGATGATGACGCCAACAACGCCAAGGCTGTGGTGAAGACCTTCCACGAG TACAGCAGGCCGTGGTGGATGATGACGCCAACGACGCCAAGGCTGTGGTGAAGACCTTCCACGAG A G CD81 Ensembl:ENSG00000110651 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs764653167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29971,Human_RBP_ID_226422,Human_RBP_ID_393891,Human_RBP_ID_1161639,Human_RBP_ID_1455744,Human_RBP_ID_1777745,Human_RBP_ID_3372641,Human_RBP_ID_5165510,Human_RBP_ID_8348623,Human_RBP_ID_9002013,Human_RBP_ID_17681758,Human_RBP_ID_18606185,Human_RBP_ID_22753295,Human_RBP_ID_23499344,Human_RBP_ID_27200481 Human_Splice_Rec_1199554,Human_Splice_Rec_1199555,Human_Splice_Rec_1199566,Human_Splice_Rec_1199574,Human_Splice_Rec_1199575,Human_Splice_Rec_1199586,Human_Splice_Rec_1199594,Human_Splice_Rec_1199595,Human_Splice_Rec_1199608,Human_Splice_Rec_1199609,Human_Splice_Rec_1199622,Human_Splice_Rec_1199623,Human_Splice_Rec_1199642,Human_Splice_Rec_1199643,Human_Splice_Rec_1199656,Human_Splice_Rec_1199657,Human_Splice_Rec_1199668,Human_Splice_Rec_1199669,Human_Splice_Rec_1199684,Human_Splice_Rec_1199685,Human_Splice_Rec_1199692,Human_Splice_Rec_1199698,Human_Splice_Rec_1199699,Human_Splice_Rec_1199706,Human_Splice_Rec_1199707 Human_miRNA_ID_2055818,Human_miRNA_ID_2171734,Human_miRNA_ID_2217897 RMVar_hsa_circ_115338,RMVar_hsa_circ_109574,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562,RMVar_hsa_circ_120379,RMVar_hsa_circ_147564,RMVar_hsa_circ_78421,RMVar_hsa_circ_7635,RMVar_hsa_circ_147565,RMVar_hsa_circ_147566,RMVar_hsa_circ_92303,RMVar_hsa_circ_110121,RMVar_hsa_circ_147567,RMVar_hsa_circ_147568 57998 RMVar_ID_57998 Human_SNP_ID_453539244 m1A Human chr11 + 2396653 2396653 2396653 CCTGCAGGAGGACTGCCACCAGAAGATCGATGACCTCTTCTCCGGGAAGCTGTACCTCATCGGCA CCTGCAGGAGGACTGCCACCAGAAGATCGATGGCCTCTTCTCCGGGAAGCTGTACCTCATCGGCA A G CD81 Ensembl:ENSG00000110651 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1281515385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393896,Human_RBP_ID_866345,Human_RBP_ID_986622,Human_RBP_ID_1354094,Human_RBP_ID_1455747,Human_RBP_ID_1777749,Human_RBP_ID_8348627,Human_RBP_ID_11584095,Human_RBP_ID_22753302,Human_RBP_ID_22790128,Human_RBP_ID_26888915 Human_Splice_Rec_1199578,Human_Splice_Rec_1199579,Human_Splice_Rec_1199598,Human_Splice_Rec_1199599,Human_Splice_Rec_1199612,Human_Splice_Rec_1199613,Human_Splice_Rec_1199626,Human_Splice_Rec_1199646,Human_Splice_Rec_1199647,Human_Splice_Rec_1199660,Human_Splice_Rec_1199672,Human_Splice_Rec_1199673,Human_Splice_Rec_1199702,Human_Splice_Rec_1199703,Human_Splice_Rec_1199710,Human_Splice_Rec_1199711,Human_Splice_Rec_1199713 RMVar_hsa_circ_1231,RMVar_hsa_circ_115338,RMVar_hsa_circ_109574,RMVar_hsa_circ_147563,RMVar_hsa_circ_113748,RMVar_hsa_circ_147562,RMVar_hsa_circ_120379,RMVar_hsa_circ_147564,RMVar_hsa_circ_78421,RMVar_hsa_circ_147565,RMVar_hsa_circ_147566,RMVar_hsa_circ_92303,RMVar_hsa_circ_110121,RMVar_hsa_circ_147567,RMVar_hsa_circ_114650,RMVar_hsa_circ_147568,RMVar_hsa_circ_147570,RMVar_hsa_circ_76351,RMVar_hsa_circ_121234,RMVar_hsa_circ_147569,RMVar_hsa_circ_147571 57999 RMVar_ID_57999 Human_SNP_ID_453539474 m1A Human chr11 - 2397200 2397200 2397200 GGACGGGCGGGCTGGGTGGACACAGCCCCCCAAGTTGGCCAAGCTGAGTCTCTGGGCGAGTGGCT GGACGGGCGGGCTGGGTGGACACAGCCCCCCAGGTTGGCCAAGCTGAGTCTCTGGGCGAGTGGCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:2397176..2397200 26863196 MeRIP-seq:(Medium) rs1049549 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6813 58000 RMVar_ID_58000 Human_SNP_ID_453539504 m1A Human chr11 - 2397296 2397296 2397296 GTGTTAGAAAGGACAGGTGCATGAAGGCAGAGAGTGCCCACAGACTCGGCTCTCGAACCGGGGCA GTGTTAGAAAGGACAGGTGCATGAAGGCAGAGTGTGCCCACAGACTCGGCTCTCGAACCGGGGCA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:2397276..2397300 26863196 MeRIP-seq:(Medium) rs1308136288 Functional Loss SNV dbSNP153 33..33 33 - - - 58001 RMVar_ID_58001 Human_SNP_ID_453541308 m1A Human chr11 - 2402725 2402725 2402725 CGGGCAAGCTGAGGTCAGAGTCCGAGTCACTGAGGGAGACTGTGTCGGAAGGCAGCGTGTCATAC CGGGCAAGCTGAGGTCAGAGTCCGAGTCACTGCGGGAGACTGTGTCGGAAGGCAGCGTGTCATAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2402675..2402958 26863196 MeRIP-seq:(Medium) rs1342954835 Functional Loss SNV dbSNP153 33..33 33 - - - 58002 RMVar_ID_58002 Human_SNP_ID_453541601 m1A Human chr11 + 2403238 2403238 2403238 GGCTGCCCCCACTGACTGCGTGTCCTCCTTCAACCAGGATCCCTCCAGCTGTGGGGAGGGGAGGG GGCTGCCCCCACTGACTGCGTGTCCTCCTTCAGCCAGGATCCCTCCAGCTGTGGGGAGGGGAGGG A G TSSC4 Ensembl:ENSG00000184281 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:2403188..2403484 32194978 MeRIP-seq:(Medium) rs752998507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344827 RMVar_hsa_circ_124786,RMVar_hsa_circ_147572,RMVar_hsa_circ_147573,RMVar_hsa_circ_120511 58003 RMVar_ID_58003 Human_SNP_ID_453555863 m1A Human chr11 - 2445294 2445294 2445294 GGCAACTGGGGGCGCGGCGGGCGCGGCCGGGGACGCAGGGGGCGCGGGACCTGGGGCGCCGGGCG GGCAACTGGGGGCGCGGCGGGCGCGGCCGGGGGCGCAGGGGGCGCGGGACCTGGGGCGCCGGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2445246..2445330 26863196 MeRIP-seq:(Medium) rs960169714 Functional Loss SNV dbSNP153 33..33 33 - - - 58004 RMVar_ID_58004 Human_SNP_ID_453645896 m1A Human chr11 + 2777715 2777714 2777715 CTTGCACAGCTGGCAGTGTGGCCAGCTTAGGCAGCCCCCTAGGGCTCTCAGAGGTCAGAGGTGGA CTTGCACAGCTGGCAGTGTGGCCAGCTTAGGC_GCCCCCTAGGGCTCTCAGAGGTCAGAGGTGGA CA C KCNQ1 Ensembl:ENSG00000053918 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:2777665..2777756 26863196 MeRIP-seq:(Medium) rs763604480 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1200041 RMVar_hsa_circ_147575,RMVar_hsa_circ_362147 58005 RMVar_ID_58005 Human_SNP_ID_453645900 m1A Human chr11 - 2777730 2777721 2777730 TCCTGCTCCACGCTCTCCACCTCTGACCTCTGAGAGCCCTAGGGGGCTGCCTAAGCTGGCCACAC TCCTGCTCCACGCTCTCCACCTCTGACCTCTG_________GGGGGCTGCCTAAGCTGGCCACAC CTAGGGCTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2777596..2777746 26863196 MeRIP-seq:(Medium) rs1224687820 Functional Loss DEL dbSNP153 33..41 33 - - - 58006 RMVar_ID_58006 Human_SNP_ID_453675610 m1A Human chr11 - 2883877 2883877 2883877 GCCCAAAGAGCCCCGAGGGAACCTGCCGGGGCAGCGGACGTTGGAAGGGCGCTGGGCCTCGGCTG GCCCAAAGAGCCCCGAGGGAACCTGCCGGGGCTGCGGACGTTGGAAGGGCGCTGGGCCTCGGCTG T A CDKN1C Ensembl:ENSG00000129757 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2883833..2884102 26863196 MeRIP-seq:(Medium) rs1336810226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200054,Human_Splice_Rec_1200058,Human_Splice_Rec_1200064,Human_Splice_Rec_1200070,Human_Splice_Rec_1200076,Human_Splice_Rec_1200078 Human_miRNA_ID_460635,Human_miRNA_ID_926306 58007 RMVar_ID_58007 Human_SNP_ID_453676210 m1A Human chr11 + 2884935 2884917 2884935 GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GCGACTGGAGCCGGG__________________GCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GGCCGGAGCCGGAGCCGGA G NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2884886..2885036 26863196 MeRIP-seq:(Medium) rs878853632 Functional Loss DEL dbSNP153 16..33 33 - - - 58008 RMVar_ID_58008 Human_SNP_ID_453676211 m1A Human chr11 + 2884935 2884917 2884935 GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GCGACTGGAGCCGGGGCCGGA____________GCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GGCCGGAGCCGGAGCCGGA GGCCGGA NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2884886..2885036 26863196 MeRIP-seq:(Medium) rs878853632 Functional Loss DEL dbSNP153 22..33 33 - - - 58009 RMVar_ID_58009 Human_SNP_ID_453676212 m1A Human chr11 + 2884935 2884917 2884935 GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GCGACTGGAGCCGGGGCCGGAGCCGGA______GCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GGCCGGAGCCGGAGCCGGA GGCCGGAGCCGGA NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2884886..2885036 26863196 MeRIP-seq:(Medium) rs878853632 Functional Loss DEL dbSNP153 28..33 33 - - - 58010 RMVar_ID_58010 Human_SNP_ID_453676234 m1A Human chr11 + 2884935 2884935 2884935 GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC A G NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2884886..2885036 26863196 MeRIP-seq:(Medium) rs191294997 Functional Loss SNV dbSNP153 33..33 33 - - - 58011 RMVar_ID_58011 Human_SNP_ID_453676523 m1A Human chr11 - 2885432 2885432 2885432 CATCCACGATGGAGCGTCTTGTCGCCCGTGGGACCTTCCCAGTACTAGTGCGCACCAGCGCCTGC CATCCACGATGGAGCGTCTTGTCGCCCGTGGGGCCTTCCCAGTACTAGTGCGCACCAGCGCCTGC T C CDKN1C Ensembl:ENSG00000129757 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2885383..2885483 32194978 MeRIP-seq:(Medium) rs1194168261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9275401 Human_Splice_Rec_1200060,Human_Splice_Rec_1200066,Human_Splice_Rec_1200072 58012 RMVar_ID_58012 Human_SNP_ID_453681513 m1A Human chr11 - 2902366 2902366 2902366 CAGAGGCCGCCCTCTCCGGAGTGTGCTCGAGTACCTGCCTTTGCAGGGGCGGGCTTGGGCACGGG CAGAGGCCGCCCTCTCCGGAGTGTGCTCGAGTTCCTGCCTTTGCAGGGGCGGGCTTGGGCACGGG T A SLC22A18AS Ensembl:ENSG00000254827 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2902325..2902440 26863196 MeRIP-seq:(Medium) rs1253620556 Functional Loss SNV dbSNP153 33..33 33 - - - 58013 RMVar_ID_58013 Human_SNP_ID_453684004 m1A Human chr11 - 2910673 2910673 2910673 CTGCTTTCTCTCATCACGGTCCCCTCTGGTCCAGCCACTGTCCTCCCCCACCTCGGCCGGCACAA CTGCTTTCTCTCATCACGGTCCCCTCTGGTCCGGCCACTGTCCTCCCCCACCTCGGCCGGCACAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2910338..2910749 26863196 MeRIP-seq:(Medium) rs1423308685 Functional Loss SNV dbSNP153 33..33 33 - - - 58014 RMVar_ID_58014 Human_SNP_ID_453694835 m1A Human chr11 + 2945080 2945078 2945081 AAAAAAAAAAAAAATCAAGAAGCAACATCCTAAGGAGAACAGGGCCCTACTCTACACAGCCCTTT AAAAAAAAAAAAAATCAAGAAGCAACATCCT___GAGAACAGGGCCCTACTCTACACAGCCCTTT TAAG T lnc-SLC22A18-1,lnc-SLC22A18-1:2 RNACentral:URS00009B4C5F,RNACentral:URS00008B7C1E lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2945030..2945131 32194978 MeRIP-seq:(Medium) rs1414036355 Functional Loss DEL dbSNP153 32..34 33 - - - 58015 RMVar_ID_58015 Human_SNP_ID_453694984 m1A Human chr11 + 2945577 2945577 2945577 CGAGGCCCCGCCCACAGGCCTGGAGTCCCGACAGCCGGTCTGCCAGGCACCCGCCTCCGCTTCCT CGAGGCCCCGCCCACAGGCCTGGAGTCCCGACTGCCGGTCTGCCAGGCACCCGCCTCCGCTTCCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2945526..2949261 32194978 MeRIP-seq:(Medium) rs574872983 Functional Loss SNV dbSNP153 33..33 33 - - - 58016 RMVar_ID_58016 Human_SNP_ID_453697230 m1A Human chr11 - 2953682 2953682 2953682 TCCCATTGTACTGAGTTCCACCAGTGGGGAGAATAGGCCAGCGTGCTCTTTATCAGCTGTTAGGT TCCCATTGTACTGAGTTCCACCAGTGGGGAGAGTAGGCCAGCGTGCTCTTTATCAGCTGTTAGGT T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2001006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6065699,Human_RBP_ID_17794275 GWAS_ID_6814,GWAS_ID_6815,GWAS_ID_6816,GWAS_ID_6817 RMVar_hsa_circ_47327,RMVar_hsa_circ_77496,RMVar_hsa_circ_126801,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147580,RMVar_hsa_circ_147581,RMVar_hsa_circ_147582,RMVar_hsa_circ_268286,RMVar_hsa_circ_268535,RMVar_hsa_circ_329952,RMVar_hsa_circ_347828,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_147583,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585 58017 RMVar_ID_58017 Human_SNP_ID_453697412 m1A Human chr11 - 2954354 2954352 2954355 TCCTTGTTGTGGGGGGAATACGCTTGAAGAGGAGAAGTCTGAGGAACAGAGCAGGAAAAGCAGGT TCCTTGTTGTGGGGGGAATACGCTTGAAGAG___AAGTCTGAGGAACAGAGCAGGAAAAGCAGGT TCTC T NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:2954351..2954551 32194978 MeRIP-seq:(Medium) rs776361840 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_394454,Human_RBP_ID_1778080,Human_RBP_ID_6065712,Human_RBP_ID_11591291,Human_RBP_ID_22790196 Human_Splice_Rec_1200348,Human_Splice_Rec_1200349 RMVar_hsa_circ_47327,RMVar_hsa_circ_77496,RMVar_hsa_circ_126801,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147580,RMVar_hsa_circ_147581,RMVar_hsa_circ_147582,RMVar_hsa_circ_268286,RMVar_hsa_circ_268535,RMVar_hsa_circ_329952,RMVar_hsa_circ_347828,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_147583,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585 58018 RMVar_ID_58018 Human_SNP_ID_453697485 m1A Human chr11 - 2954529 2954529 2954529 ACTTCACTGGGGAGGCCATAGAAGATGATGACAATGTATGAGGCTCGGGGAAGGGGGGCTTCCAC ACTTCACTGGGGAGGCCATAGAAGATGATGACCATGTATGAGGCTCGGGGAAGGGGGGCTTCCAC T G NAP1L4 Ensembl:ENSG00000205531 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:2954526..2954575;chr11:2954526..2954550 26863196 MeRIP-seq:(Medium) rs1404698959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6065719,Human_RBP_ID_11591307,Human_RBP_ID_17794283,Human_RBP_ID_18973224,Human_RBP_ID_19048995,Human_RBP_ID_22896102,Human_RBP_ID_23500521,Human_RBP_ID_24880369,Human_RBP_ID_26317759 Human_Splice_Rec_1200249,Human_Splice_Rec_1200275,Human_Splice_Rec_1200317,Human_Splice_Rec_1200325,Human_Splice_Rec_1200347 RMVar_hsa_circ_47327,RMVar_hsa_circ_77496,RMVar_hsa_circ_126801,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147580,RMVar_hsa_circ_147581,RMVar_hsa_circ_147582,RMVar_hsa_circ_268286,RMVar_hsa_circ_268535,RMVar_hsa_circ_329952,RMVar_hsa_circ_347828,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_147583,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585,RMVar_hsa_circ_147586,RMVar_hsa_circ_92505 58019 RMVar_ID_58019 Human_SNP_ID_453698404 m1A Human chr11 + 2957904 2957904 2957904 TAAAAAATTACAAGAAAAGGGGGACTAAGCAGATGATCCAAAAGCAGCACAACTAGAACCAGCGT TAAAAAATTACAAGAAAAGGGGGACTAAGCAGGTGATCCAAAAGCAGCACAACTAGAACCAGCGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:2957897..2958010 32194978 MeRIP-seq:(Medium) rs1034394680 Functional Loss SNV dbSNP153 33..33 33 - - - 58020 RMVar_ID_58020 Human_SNP_ID_453708367 m1A Human chr11 + 2991614 2991614 2991614 GCCGCCCAGCTCGCTCCCACCGCACAGCTCCCAACAGCTAAGAAGCAACGCCAAGGACTTTCTTC GCCGCCCAGCTCGCTCCCACCGCACAGCTCCCTACAGCTAAGAAGCAACGCCAAGGACTTTCTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2991610..2991686 26863196 MeRIP-seq:(Medium) rs1293677305 Functional Loss SNV dbSNP153 33..33 33 - - - 58021 RMVar_ID_58021 Human_SNP_ID_453708410 m1A Human chr11 + 2991746 2991746 2991746 CAGAGGCTCACGATGACAACCGCCCTACGGAAAAACTCAAATTCCTAAACATCTAATAAAGAAGT CAGAGGCTCACGATGACAACCGCCCTACGGAATAACTCAAATTCCTAAACATCTAATAAAGAAGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2991744..2992354 26863196 MeRIP-seq:(Medium) rs930025407 Functional Loss SNV dbSNP153 33..33 33 - - - 58022 RMVar_ID_58022 Human_SNP_ID_453708613 m1A Human chr11 - 2992245 2992245 2992245 CGCCACTGCCGCAGGAGGCGTGAGGTGCGGAGACACGGGTGCTGGGCCGGTAACGGCGCGCTGGG CGCCACTGCCGCAGGAGGCGTGAGGTGCGGAGGCACGGGTGCTGGGCCGGTAACGGCGCGCTGGG T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr11:2991986..2992246;chr11:2992076..2992300 26863196 MeRIP-seq:(Medium) rs1448386473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416503,Human_RBP_ID_19050896 Human_Splice_Rec_1200423,Human_Splice_Rec_1200435,Human_Splice_Rec_1200461,Human_Splice_Rec_1200471,Human_Splice_Rec_1200493 RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585 58023 RMVar_ID_58023 Human_SNP_ID_453711530 m1A Human chr11 + 3002599 3002599 3002599 CCTCCTCTTTCTTCTTCCTCTTCTCCTCTTCAACCTGGAGGGTCAATACAGAGCCAGATGAGACA CCTCCTCTTTCTTCTTCCTCTTCTCCTCTTCATCCTGGAGGGTCAATACAGAGCCAGATGAGACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3002485..3002635 26863196 MeRIP-seq:(Medium) rs1007523733 Functional Loss SNV dbSNP153 33..33 33 - - - 58024 RMVar_ID_58024 Human_SNP_ID_453712226 m1A Human chr11 - 3005315 3005315 3005315 ACTTAAGCGTGATATTTGTTGAAAATGTAAAAACCATTGCGATTATTACATAGTTTACTTTTTAA ACTTAAGCGTGATATTTGTTGAAAATGTAAAATCCATTGCGATTATTACATAGTTTACTTTTTAA T A CARS1 Ensembl:ENSG00000110619 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3005312..3005450 26863196 MeRIP-seq:(Medium) rs757679888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147601,RMVar_hsa_circ_110417,RMVar_hsa_circ_127125,RMVar_hsa_circ_147600,RMVar_hsa_circ_147602 58025 RMVar_ID_58025 Human_SNP_ID_453713067 m1A Human chr11 + 3008150 3008149 3008150 ACTGTGCTAGGCGGGCAGGTGCCCTGCCCCCCAGCCTGCTGGGACCCCCACCATCCCACCCCATC ACTGTGCTAGGCGGGCAGGTGCCCTGCCCCCC_GCCTGCTGGGACCCCCACCATCCCACCCCATC CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3008147..3008237 26863196 MeRIP-seq:(Medium) rs201258638 Functional Loss DEL dbSNP153 33..33 33 - - - 58026 RMVar_ID_58026 Human_SNP_ID_453726521 m1A Human chr11 - 3057027 3057027 3057027 GAGGGGTGGCACGTCCTAGGATCCGAAGGACAACGGGTGCCCGGCTCCGAGGGACGGCCACTGGG GAGGGGTGGCACGTCCTAGGATCCGAAGGACAGCGGGTGCCCGGCTCCGAGGGACGGCCACTGGG T C CARS1 Ensembl:ENSG00000110619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3057023..3057388 26863196 MeRIP-seq:(Medium) rs1026333457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3384045,Human_RBP_ID_8064115,Human_RBP_ID_26775565 RMVar_hsa_circ_95792,RMVar_hsa_circ_147608 58027 RMVar_ID_58027 Human_SNP_ID_453726786 m1A Human chr11 - 3057652 3057652 3057652 AGCGCAATCATGACTTAAACACCTATTACAGGACGCTCAGTCTTTAGTGCTTGTCTCCCCGCGGC AGCGCAATCATGACTTAAACACCTATTACAGGGCGCTCAGTCTTTAGTGCTTGTCTCCCCGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3057601..3057692 26863196 MeRIP-seq:(Medium) rs1201259359 Functional Loss SNV dbSNP153 33..33 33 - - - 58028 RMVar_ID_58028 Human_SNP_ID_453736714 m1A Human chr11 - 3093588 3093588 3093588 CGCTTTTCTGGACCCCGAGCGGGGAGGTCCGCAGACAGAGGCTGAGGCAGCACACGGTGCCGCTG CGCTTTTCTGGACCCCGAGCGGGGAGGTCCGCGGACAGAGGCTGAGGCAGCACACGGTGCCGCTG T C OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3093481..3093627 26863196 MeRIP-seq:(Medium) rs1289615353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200866,Human_Splice_Rec_1200867,Human_Splice_Rec_1200880,Human_Splice_Rec_1200881,Human_Splice_Rec_1200918,Human_Splice_Rec_1200919,Human_Splice_Rec_1200936,Human_Splice_Rec_1200937,Human_Splice_Rec_1200978,Human_Splice_Rec_1200979,Human_Splice_Rec_1201008,Human_Splice_Rec_1201009,Human_Splice_Rec_1201046,Human_Splice_Rec_1201047,Human_Splice_Rec_1201086 RMVar_hsa_circ_147611,RMVar_hsa_circ_99648 58029 RMVar_ID_58029 Human_SNP_ID_453736719 m1A Human chr11 + 3093593 3093593 3093593 GCACCGTGTGCTGCCTCAGCCTCTGTCTGCGGACCTCCCCGCTCGGGGTCCAGAAAAGCGCACTG GCACCGTGTGCTGCCTCAGCCTCTGTCTGCGGGCCTCCCCGCTCGGGGTCCAGAAAAGCGCACTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3093525..3093760 26863196 MeRIP-seq:(Medium) rs1271517604 Functional Loss SNV dbSNP153 33..33 33 - - - 58030 RMVar_ID_58030 Human_SNP_ID_453739887 m1A Human chr11 - 3103630 3103626 3103631 GAGGCAGGAAGGGGGCTGCAGGCTCAGGAGCCAGGCAGAGGGAGCAGGTGGGAACAAGAGCATGG GAGGCAGGAAGGGGGCTGCAGGCTCAGGAGC_____AGAGGGAGCAGGTGGGAACAAGAGCATGG TGCCTG T OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3103620..3103832 26863196 MeRIP-seq:(Medium) rs1466462740 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_147611,RMVar_hsa_circ_99648,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613 58031 RMVar_ID_58031 Human_SNP_ID_453739914 m1A Human chr11 + 3103677 3103677 3103677 CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCCGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3103668..3103809 26863196 MeRIP-seq:(Medium) rs1163821924 Functional Loss SNV dbSNP153 33..33 33 - - - 58032 RMVar_ID_58032 Human_SNP_ID_453739915 m1A Human chr11 + 3103677 3103677 3103677 CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCGGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3103668..3103809 26863196 MeRIP-seq:(Medium) rs1163821924 Functional Loss SNV dbSNP153 33..33 33 - - - 58033 RMVar_ID_58033 Human_SNP_ID_453739916 m1A Human chr11 + 3103677 3103677 3103677 CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC CAGCCCCCTTCCTGCCTCTGTTGCCCCCTTCCTGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3103668..3103809 26863196 MeRIP-seq:(Medium) rs1163821924 Functional Loss SNV dbSNP153 33..33 33 - - - 58034 RMVar_ID_58034 Human_SNP_ID_453739947 m1A Human chr11 + 3103697 3103694 3103698 TTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCCCCTTCCAGGCTCTGCTGCCC TTGCCCCCTTCCAGTCTCTGCAGCCCCCTT____CCTGCGTACCCCCTTCCAGGCTCTGCTGCCC TCCAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3103660..3103819 26863196 MeRIP-seq:(Medium) rs1233763311 Functional Loss DEL dbSNP153 31..34 33 - - - 58035 RMVar_ID_58035 Human_SNP_ID_453739948 m1A Human chr11 + 3103697 3103697 3103697 TTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCAGCCTGCGTACCCCCTTCCAGGCTCTGCTGCCC TTGCCCCCTTCCAGTCTCTGCAGCCCCCTTCCTGCCTGCGTACCCCCTTCCAGGCTCTGCTGCCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3103660..3103819 26863196 MeRIP-seq:(Medium) rs1161017500 Functional Loss SNV dbSNP153 33..33 33 - - - 58036 RMVar_ID_58036 Human_SNP_ID_453740677 m1A Human chr11 - 3104345 3104345 3104345 CTGGGCGAGGCGTCCCAGGTGGAGACAGTGTCAGAGGAGAACAAGAGTCTGATGTGGACCCTGCT CTGGGCGAGGCGTCCCAGGTGGAGACAGTGTCCGAGGAGAACAAGAGTCTGATGTGGACCCTGCT T G OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3104253..3104412 26863196 MeRIP-seq:(Medium) rs1226412887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200854,Human_Splice_Rec_1200906,Human_Splice_Rec_1200966,Human_Splice_Rec_1201034,Human_Splice_Rec_1201074 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_147611,RMVar_hsa_circ_99648,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920 58037 RMVar_ID_58037 Human_SNP_ID_453740679 m1A Human chr11 + 3104349 3104349 3104349 GGGTCCACATCAGACTCTTGTTCTCCTCTGACACTGTCTCCACCTGGGACGCCTCGCCCAGCTGC GGGTCCACATCAGACTCTTGTTCTCCTCTGACGCTGTCTCCACCTGGGACGCCTCGCCCAGCTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3104298..3107413 26863196 MeRIP-seq:(Medium) rs765910962 Functional Loss SNV dbSNP153 33..33 33 - - - 58038 RMVar_ID_58038 Human_SNP_ID_453740977 m1A Human chr11 - 3105554 3105554 3105554 TACGGCAAGACAGTCTCAGTAGAGAAGACGGCAGAAGCCTGGTGGAGAGGGTTAAGGAGGACGGG TACGGCAAGACAGTCTCAGTAGAGAAGACGGCGGAAGCCTGGTGGAGAGGGTTAAGGAGGACGGG T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3105552..3105692 26863196 MeRIP-seq:(Medium) rs560693896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920 58039 RMVar_ID_58039 Human_SNP_ID_453741315 m1A Human chr11 - 3106650 3106647 3106650 AGTGACGGGAGGGAGGATGGCGTTCCAAGAAGAAGGACCACCAGCGCACGAGCTCAAGGGAGGCA AGTGACGGGAGGGAGGATGGCGTTCCAAGAAG___GACCACCAGCGCACGAGCTCAAGGGAGGCA CCTT C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3106640..3106777 26863196 MeRIP-seq:(Medium) rs1418908215 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920 58040 RMVar_ID_58040 Human_SNP_ID_453741502 m1A Human chr11 + 3107270 3107270 3107270 GGGCTCCTGGCTGGGGGGCTCTCACCTCCCCCAGCTCCTCCTGGACCTGCTCCACATAGGTGGTC GGGCTCCTGGCTGGGGGGCTCTCACCTCCCCCGGCTCCTCCTGGACCTGCTCCACATAGGTGGTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3107266..3107380 26863196 MeRIP-seq:(Medium) rs111469886 Functional Loss SNV dbSNP153 33..33 33 - - - 58041 RMVar_ID_58041 Human_SNP_ID_453742228 m1A Human chr11 - 3109476 3109476 3109476 AAAACTCACTGTCTCCAGGAGCTCGAAAAGGCAGAGGCTCAGAGAGGCACAGAACCGCCTTCAAT AAAACTCACTGTCTCCAGGAGCTCGAAAAGGCTGAGGCTCAGAGAGGCACAGAACCGCCTTCAAT T A OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:3109426..3109575 26863196 MeRIP-seq:(Medium) rs1198498707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_147615 58042 RMVar_ID_58042 Human_SNP_ID_453742239 m1A Human chr11 - 3109501 3109498 3109502 TTAATGGATCTCAAAGTGAGGGAGAAAAACTCACTGTCTCCAGGAGCTCGAAAAGGCAGAGGCTC TTAATGGATCTCAAAGTGAGGGAGAAAAACT____GTCTCCAGGAGCTCGAAAAGGCAGAGGCTC CAGTG C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3109476..3109500 26863196 MeRIP-seq:(Medium) rs1303353538 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_147615 58043 RMVar_ID_58043 Human_SNP_ID_453742336 m1A Human chr11 - 3109892 3109891 3109892 GAGGAGAGGTGTCTGCAGCCCCTGTGGGTATCAGGGTGGGCTTCCAGGAAGAGGAGGAAGAGGTC GAGGAGAGGTGTCTGCAGCCCCTGTGGGTATC_GGGTGGGCTTCCAGGAAGAGGAGGAAGAGGTC CT C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:3109841..3109983;chr11:3109841..3110032 26863196 MeRIP-seq:(Medium) rs1268768401 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23501307 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_15738,RMVar_hsa_circ_147613,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_147615 58044 RMVar_ID_58044 Human_SNP_ID_453745358 m1A Human chr11 - 3119653 3119653 3119653 TGCAGCTGGCCCTGGGTGTTGCCTCGGGTGACACCCAGATCTCTCTCTCTCCAGGGCCCCAAAGG TGCAGCTGGCCCTGGGTGTTGCCTCGGGTGACGCCCAGATCTCTCTCTCTCCAGGGCCCCAAAGG T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:3119651..3119675 26863196 MeRIP-seq:(Medium) rs753037886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22640863 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_323218,RMVar_hsa_circ_147615,RMVar_hsa_circ_25265,RMVar_hsa_circ_147616,RMVar_hsa_circ_147617 58045 RMVar_ID_58045 Human_SNP_ID_453745359 m1A Human chr11 - 3119653 3119653 3119653 TGCAGCTGGCCCTGGGTGTTGCCTCGGGTGACACCCAGATCTCTCTCTCTCCAGGGCCCCAAAGG TGCAGCTGGCCCTGGGTGTTGCCTCGGGTGACCCCCAGATCTCTCTCTCTCCAGGGCCCCAAAGG T G OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:3119651..3119675 26863196 MeRIP-seq:(Medium) rs753037886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22640863 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_323218,RMVar_hsa_circ_147615,RMVar_hsa_circ_25265,RMVar_hsa_circ_147616,RMVar_hsa_circ_147617 58046 RMVar_ID_58046 Human_SNP_ID_453746302 m1A Human chr11 - 3122424 3122424 3122424 GTCCCGCATACCCACCTCTCTCTTTCAGGCAGAGTACAGGCTGTGCAACGGGTCAGACAAGGAAT GTCCCGCATACCCACCTCTCTCTTTCAGGCAGGGTACAGGCTGTGCAACGGGTCAGACAAGGAAT T C OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3122347..3122475 26863196 MeRIP-seq:(Medium) rs1211347684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29269 Human_Splice_Rec_1200842,Human_Splice_Rec_1200843,Human_Splice_Rec_1200896,Human_Splice_Rec_1200897,Human_Splice_Rec_1200954,Human_Splice_Rec_1200955,Human_Splice_Rec_1200994,Human_Splice_Rec_1200995,Human_Splice_Rec_1201024,Human_Splice_Rec_1201025,Human_Splice_Rec_1201062,Human_Splice_Rec_1201063,Human_Splice_Rec_1201090,Human_Splice_Rec_1201091,Human_Splice_Rec_1201102,Human_Splice_Rec_1201103,Human_Splice_Rec_1201112,Human_Splice_Rec_1201113,Human_Splice_Rec_1201116,Human_Splice_Rec_1201120,Human_Splice_Rec_1201121,Human_Splice_Rec_1201128,Human_Splice_Rec_1201134 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_147615,RMVar_hsa_circ_25265,RMVar_hsa_circ_23876,RMVar_hsa_circ_147617,RMVar_hsa_circ_24776 58047 RMVar_ID_58047 Human_SNP_ID_453746303 m1A Human chr11 - 3122426 3122426 3122426 CTGTCCCGCATACCCACCTCTCTCTTTCAGGCAGAGTACAGGCTGTGCAACGGGTCAGACAAGGA CTGTCCCGCATACCCACCTCTCTCTTTCAGGCGGAGTACAGGCTGTGCAACGGGTCAGACAAGGA T C OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:3122326..3122450;chr11:3122306..3122450 26863196 MeRIP-seq:(Medium) rs1162169759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29269 Human_Splice_Rec_1200842,Human_Splice_Rec_1200843,Human_Splice_Rec_1200896,Human_Splice_Rec_1200897,Human_Splice_Rec_1200954,Human_Splice_Rec_1200955,Human_Splice_Rec_1200994,Human_Splice_Rec_1200995,Human_Splice_Rec_1201024,Human_Splice_Rec_1201025,Human_Splice_Rec_1201062,Human_Splice_Rec_1201063,Human_Splice_Rec_1201090,Human_Splice_Rec_1201091,Human_Splice_Rec_1201102,Human_Splice_Rec_1201103,Human_Splice_Rec_1201112,Human_Splice_Rec_1201113,Human_Splice_Rec_1201116,Human_Splice_Rec_1201120,Human_Splice_Rec_1201121,Human_Splice_Rec_1201128,Human_Splice_Rec_1201134 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_88590,RMVar_hsa_circ_147615,RMVar_hsa_circ_25265,RMVar_hsa_circ_23876,RMVar_hsa_circ_147617,RMVar_hsa_circ_24776 58048 RMVar_ID_58048 Human_SNP_ID_453746305 m1A Human chr11 - 3122430 3122430 3122430 TGCCCTGTCCCGCATACCCACCTCTCTCTTTCAGGCAGAGTACAGGCTGTGCAACGGGTCAGACA TGCCCTGTCCCGCATACCCACCTCTCTCTTTCGGGCAGAGTACAGGCTGTGCAACGGGTCAGACA T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr11:3122326..3122450;chr11:3122401..3122450 26863196 MeRIP-seq:(Medium) rs1564844074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200843,Human_Splice_Rec_1200897,Human_Splice_Rec_1200955,Human_Splice_Rec_1200995,Human_Splice_Rec_1201025,Human_Splice_Rec_1201063,Human_Splice_Rec_1201091,Human_Splice_Rec_1201103,Human_Splice_Rec_1201113,Human_Splice_Rec_1201121 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_25265,RMVar_hsa_circ_23876,RMVar_hsa_circ_147617,RMVar_hsa_circ_24776 58049 RMVar_ID_58049 Human_SNP_ID_453747477 m1A Human chr11 - 3126512 3126512 3126512 GAGCCCAACGGCCCGTCGCTGCCCAGGGATGAAGGGCCCCCGACCCCAAGCTCTGCCACGAAGGT GAGCCCAACGGCCCGTCGCTGCCCAGGGATGAGGGGCCCCCGACCCCAAGCTCTGCCACGAAGGT T C OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3126436..3126636 26863196 MeRIP-seq:(Medium) rs1232074148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200840,Human_Splice_Rec_1200841,Human_Splice_Rec_1200894,Human_Splice_Rec_1200895,Human_Splice_Rec_1200953,Human_Splice_Rec_1200992,Human_Splice_Rec_1200993,Human_Splice_Rec_1201022,Human_Splice_Rec_1201023,Human_Splice_Rec_1201060,Human_Splice_Rec_1201061,Human_Splice_Rec_1201089,Human_Splice_Rec_1201100,Human_Splice_Rec_1201101,Human_Splice_Rec_1201110,Human_Splice_Rec_1201111,Human_Splice_Rec_1201115,Human_Splice_Rec_1201118,Human_Splice_Rec_1201119,Human_Splice_Rec_1201126,Human_Splice_Rec_1201127,Human_Splice_Rec_1201132,Human_Splice_Rec_1201133,Human_Splice_Rec_1201138 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_25265,RMVar_hsa_circ_23876,RMVar_hsa_circ_147617,RMVar_hsa_circ_24776,RMVar_hsa_circ_53198 58050 RMVar_ID_58050 Human_SNP_ID_453747483 m1A Human chr11 - 3126520 3126520 3126520 AGGACATGGAGCCCAACGGCCCGTCGCTGCCCAGGGATGAAGGGCCCCCGACCCCAAGCTCTGCC AGGACATGGAGCCCAACGGCCCGTCGCTGCCCCGGGATGAAGGGCCCCCGACCCCAAGCTCTGCC T G OSBPL5 Ensembl:ENSG00000021762 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:3126374..3126700;chr11:3126424..3126700;chr11:3126412..3129211 26863196 MeRIP-seq:(Medium) rs752982529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200840,Human_Splice_Rec_1200841,Human_Splice_Rec_1200894,Human_Splice_Rec_1200895,Human_Splice_Rec_1200953,Human_Splice_Rec_1200992,Human_Splice_Rec_1200993,Human_Splice_Rec_1201022,Human_Splice_Rec_1201023,Human_Splice_Rec_1201060,Human_Splice_Rec_1201061,Human_Splice_Rec_1201089,Human_Splice_Rec_1201100,Human_Splice_Rec_1201101,Human_Splice_Rec_1201110,Human_Splice_Rec_1201111,Human_Splice_Rec_1201115,Human_Splice_Rec_1201118,Human_Splice_Rec_1201119,Human_Splice_Rec_1201126,Human_Splice_Rec_1201127,Human_Splice_Rec_1201132,Human_Splice_Rec_1201133,Human_Splice_Rec_1201138 RMVar_hsa_circ_28666,RMVar_hsa_circ_147612,RMVar_hsa_circ_375574,RMVar_hsa_circ_295266,RMVar_hsa_circ_147613,RMVar_hsa_circ_419,RMVar_hsa_circ_34342,RMVar_hsa_circ_147614,RMVar_hsa_circ_91920,RMVar_hsa_circ_25265,RMVar_hsa_circ_23876,RMVar_hsa_circ_147617,RMVar_hsa_circ_24776,RMVar_hsa_circ_53198 58051 RMVar_ID_58051 Human_SNP_ID_453748882 m1A Human chr11 + 3131505 3131505 3131505 CGTCCATCCATCCATCCATCTACCATCCTCCCATCTATCCATCCATCCACCCATTCATCCATCCA CGTCCATCCATCCATCCATCTACCATCCTCCCGTCTATCCATCCATCCACCCATTCATCCATCCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3131403..3131646 26863196 MeRIP-seq:(Medium) rs888886759 Functional Loss SNV dbSNP153 33..33 33 - - - 58052 RMVar_ID_58052 Human_SNP_ID_453753591 m1A Human chr11 + 3147653 3147653 3147653 TGGACTTCCAGAAATTTACCCTTGGGACTAAAACCCCCTGTAATCAATATCTGCTGGAAGAGAGG TGGACTTCCAGAAATTTACCCTTGGGACTAAACCCCCCTGTAATCAATATCTGCTGGAAGAGAGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:3147651..3147834 26863196 MeRIP-seq:(Medium) rs1031623134 Functional Loss SNV dbSNP153 33..33 33 - - - 58053 RMVar_ID_58053 Human_SNP_ID_453757627 m1A Human chr11 + 3162598 3162598 3162598 GTCCAAGTCCTTTGTACTCGACCGCCAACCCTACCACTCTCCGGAGCAGCTTCACTATCTGCCCA GTCCAAGTCCTTTGTACTCGACCGCCAACCCTGCCACTCTCCGGAGCAGCTTCACTATCTGCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3162596..3162689 26863196 MeRIP-seq:(Medium) rs1416860920 Functional Loss SNV dbSNP153 33..33 33 - - - 58054 RMVar_ID_58054 Human_SNP_ID_453758354 m1A Human chr11 - 3165187 3165187 3165187 GGAGGTAGGAGCGCGGCGGCCCGGGGGGCGGCAGGGCGGCGGGGGGATGGCGGGCTGGGAAGGAT GGAGGTAGGAGCGCGGCGGCCCGGGGGGCGGCGGGGCGGCGGGGGGATGGCGGGCTGGGAAGGAT T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:3165176..3165261 26863410 MeRIP-seq:(Medium) rs531628959 Functional Loss SNV dbSNP153 33..33 33 - - - 58055 RMVar_ID_58055 Human_SNP_ID_453758386 m1A Human chr11 - 3165268 3165268 3165268 ATTTCCTGCAGCCAGGCCCGCGCCGCCAGTGGAGCCCCCGCGCGCCCGGCCGGCCCGGAGCACCG ATTTCCTGCAGCCAGGCCCGCGCCGCCAGTGGCGCCCCCGCGCGCCCGGCCGGCCCGGAGCACCG T G OSBPL5 Ensembl:ENSG00000021762 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr11:3164851..3165350;chr11:3164951..3165350;chr11:3164871..3165350 26863196 MeRIP-seq:(Medium) rs1215988507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1200837,Human_Splice_Rec_1200891,Human_Splice_Rec_1200989,Human_Splice_Rec_1201019,Human_Splice_Rec_1201097,Human_Splice_Rec_1201107,Human_Splice_Rec_1201139 58056 RMVar_ID_58056 Human_SNP_ID_453759748 m1A Human chr11 - 3169970 3169967 3169971 TGCACACGTGTGCATCAGAGAGAGAGACAGACAGAGACACAGAGTAAGAGAGTCAGAGAGAGACA TGCACACGTGTGCATCAGAGAGAGAGACAGA____GACACAGAGTAAGAGAGTCAGAGAGAGACA CTCTG C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:3169914..3170001 26863410 MeRIP-seq:(Medium) rs1201512660 Functional Loss DEL dbSNP153 32..35 33 - - - 58057 RMVar_ID_58057 Human_SNP_ID_453770006 m1A Human chr11 + 3206828 3206800 3206828 TAATGGTGGTGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATG TAATG____________________________TAATGGTGATGATGGTGATAATGGTGATGATG GGTGGTGATGGTGATGATGGTGATGATGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3206697..3206894 26863196 MeRIP-seq:(Medium) rs1157223047 Functional Loss DEL dbSNP153 6..33 33 - - - 58058 RMVar_ID_58058 Human_SNP_ID_453770011 m1A Human chr11 + 3206837 3206804 3206837 TGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATGGTAATGGTG _________________________________TGATGGTGATAATGGTGATGATGGTAATGGTG GTGATGGTGATGATGGTGATGATGATAATGGTGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3206750..3206884 26863196 MeRIP-seq:(Medium) rs1564884547 Functional Loss DEL dbSNP153 1..33 33 - - - 58059 RMVar_ID_58059 Human_SNP_ID_453770031 m1A Human chr11 + 3206828 3206828 3206828 TAATGGTGGTGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATG TAATGGTGGTGATGGTGATGATGGTGATGATGGTAATGGTGATGATGGTGATAATGGTGATGATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3206697..3206894 26863196 MeRIP-seq:(Medium) rs1007385734 Functional Loss SNV dbSNP153 33..33 33 - - - 58060 RMVar_ID_58060 Human_SNP_ID_453770034 m1A Human chr11 + 3206837 3206834 3206837 TGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATGGTAATGGTG TGATGGTGATGATGGTGATGATGATAATGG___TGATGGTGATAATGGTGATGATGGTAATGGTG GTGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3206750..3206884 26863196 MeRIP-seq:(Medium) rs1342185822 Functional Loss DEL dbSNP153 31..33 33 - - - 58061 RMVar_ID_58061 Human_SNP_ID_453770036 m1A Human chr11 + 3206837 3206837 3206837 TGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATGGTAATGGTG TGATGGTGATGATGGTGATGATGATAATGGTGGTGATGGTGATAATGGTGATGATGGTAATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3206750..3206884 26863196 MeRIP-seq:(Medium) rs750715477 Functional Loss SNV dbSNP153 33..33 33 - - - 58062 RMVar_ID_58062 Human_SNP_ID_453799167 m1A Human chr11 - 3370960 3370960 3370960 CAGCAGACGGACATCCAGGTGGGTGGGAATGAACGAAGCAGGTAACCCAGGTGAGAGGTCCAGAG CAGCAGACGGACATCCAGGTGGGTGGGAATGAGCGAAGCAGGTAACCCAGGTGAGAGGTCCAGAG T C ZNF195 Ensembl:ENSG00000005801 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3370883..3371005 26863196 MeRIP-seq:(Medium) rs375518869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807004,Human_RBP_ID_867098,Human_RBP_ID_9361938,Human_RBP_ID_11604782,Human_RBP_ID_18973231,Human_RBP_ID_19049015,Human_RBP_ID_22895640,Human_RBP_ID_27836285 Human_Splice_Rec_1201279 RMVar_hsa_circ_7397 58063 RMVar_ID_58063 Human_SNP_ID_453801106 m1A Human chr11 - 3379075 3379075 3379075 AGGTCGTGTGACCCGCAGGCACCGGGAGATCCAGAAGTGAAACGCCAGGCTCTCTGGAGGCCAGG AGGTCGTGTGACCCGCAGGCACCGGGAGATCCGGAAGTGAAACGCCAGGCTCTCTGGAGGCCAGG T C ZNF195 Ensembl:ENSG00000005801 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3378885..3379076 26863196 MeRIP-seq:(Medium) rs1396098546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395485,Human_RBP_ID_1462455,Human_RBP_ID_4184606,Human_RBP_ID_11604988,Human_RBP_ID_18416504,Human_RBP_ID_18971680,Human_RBP_ID_27804219 Human_Splice_Rec_1201161,Human_Splice_Rec_1201167,Human_Splice_Rec_1201173,Human_Splice_Rec_1201183,Human_Splice_Rec_1201191,Human_Splice_Rec_1201203,Human_Splice_Rec_1201211,Human_Splice_Rec_1201221,Human_Splice_Rec_1201229,Human_Splice_Rec_1201239,Human_Splice_Rec_1201249,Human_Splice_Rec_1201259,Human_Splice_Rec_1201275,Human_Splice_Rec_1201283,Human_Splice_Rec_1201305,Human_Splice_Rec_1201319,Human_Splice_Rec_1201327,Human_Splice_Rec_1201337,Human_Splice_Rec_1201347,Human_Splice_Rec_1201357,Human_Splice_Rec_1201365,Human_Splice_Rec_1201373,Human_Splice_Rec_1201379,Human_Splice_Rec_1201389,Human_Splice_Rec_1201397,Human_Splice_Rec_1201403 58064 RMVar_ID_58064 Human_SNP_ID_453815874 m1A Human chr11 + 3423401 3423401 3423401 GGAGAGTTTGAGGCAGGCCCAGGAGCGAGCCCACGGTCTGCCGACGCGGAGCCAGGGACGGGCCC GGAGAGTTTGAGGCAGGCCCAGGAGCGAGCCCGCGGTCTGCCGACGCGGAGCCAGGGACGGGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3423351..3423503 26863196 MeRIP-seq:(Medium) rs1206273108 Functional Loss SNV dbSNP153 33..33 33 - - - 58065 RMVar_ID_58065 Human_SNP_ID_453858387 m1A Human chr11 + 3545012 3545011 3545013 ACAGAAAGTGAGACTGGGGAGAGAGATAGTGTAAGAGAGAGAGAGAGAGACCGTAAGAGAAGGGA ACAGAAAGTGAGACTGGGGAGAGAGATAGTGT__GAGAGAGAGAGAGAGACCGTAAGAGAAGGGA TAA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3544853..3545143 26863196 MeRIP-seq:(Medium) rs201177799 Functional Loss DEL dbSNP153 33..34 33 - - - 58066 RMVar_ID_58066 Human_SNP_ID_453858388 m1A Human chr11 + 3545012 3545012 3545012 ACAGAAAGTGAGACTGGGGAGAGAGATAGTGTAAGAGAGAGAGAGAGAGACCGTAAGAGAAGGGA ACAGAAAGTGAGACTGGGGAGAGAGATAGTGTGAGAGAGAGAGAGAGAGACCGTAAGAGAAGGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3544853..3545143 26863196 MeRIP-seq:(Medium) rs955115515 Functional Loss SNV dbSNP153 33..33 33 - - - 58067 RMVar_ID_58067 Human_SNP_ID_453858431 m1A Human chr11 - 3545128 3545128 3545128 GTGTGGGTGCTGCGGCACCCGGGCAGTCTCCCACTTCCTTTGTGTCTTAGTTGCTGTTTCTCATC GTGTGGGTGCTGCGGCACCCGGGCAGTCTCCCGCTTCCTTTGTGTCTTAGTTGCTGTTTCTCATC T C AC127526.2 Ensembl:ENSG00000255367 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3545003..3545130 26863196 MeRIP-seq:(Medium) rs528033258 Functional Loss SNV dbSNP153 33..33 33 - - - 58068 RMVar_ID_58068 Human_SNP_ID_453858432 m1A Human chr11 - 3545128 3545128 3545128 GTGTGGGTGCTGCGGCACCCGGGCAGTCTCCCACTTCCTTTGTGTCTTAGTTGCTGTTTCTCATC GTGTGGGTGCTGCGGCACCCGGGCAGTCTCCCCCTTCCTTTGTGTCTTAGTTGCTGTTTCTCATC T G AC127526.2 Ensembl:ENSG00000255367 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3545003..3545130 26863196 MeRIP-seq:(Medium) rs528033258 Functional Loss SNV dbSNP153 33..33 33 - - - 58069 RMVar_ID_58069 Human_SNP_ID_453869502 m1A Human chr11 - 3581151 3581151 3581151 CGCCGGGTCCTTCCTCTTCCCCAGGTGCAGGCAGAACCCCCGGAGCCATGGCCAGCCCTTCCGGC CGCCGGGTCCTTCCTCTTCCCCAGGTGCAGGCTGAACCCCCGGAGCCATGGCCAGCCCTTCCGGC T A AC127526.2 Ensembl:ENSG00000255367 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:3581102..3581248;chr11:3581081..3581209;chr11:3581086..3581272 26863196 MeRIP-seq:(Medium) rs1247959727 Functional Loss SNV dbSNP153 33..33 33 - - - 58070 RMVar_ID_58070 Human_SNP_ID_453880243 m1A Human chr11 + 3616110 3616110 3616110 GGGGAGGGCAAAGCGGGAGGATTGGTGAAGAAAGAGTATGTTGGGATCCTGCTGGGGCCCTGGTC GGGGAGGGCAAAGCGGGAGGATTGGTGAAGAAGGAGTATGTTGGGATCCTGCTGGGGCCCTGGTC A G TRPC2 Ensembl:ENSG00000182048 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3615960..3616171 26863196 MeRIP-seq:(Medium) rs547551972 Functional Loss SNV dbSNP153 33..33 33 - - - 58071 RMVar_ID_58071 Human_SNP_ID_453916502 m1A Human chr11 - 3735315 3735315 3735315 TTTTCTTTTTTTTTTTTTAAAAGCTTTGACAGATCCAAATGCTTCTGCTGCCCAGCAGGCTGTTC TTTTCTTTTTTTTTTTTTAAAAGCTTTGACAGCTCCAAATGCTTCTGCTGCCCAGCAGGCTGTTC T G NUP98 Ensembl:ENSG00000110713 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:3735211..3760142 32194978 MeRIP-seq:(Medium) rs760832963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30033,Human_RBP_ID_864765,Human_RBP_ID_22790335,Human_RBP_ID_24913231 Human_Splice_Rec_1201644,Human_Splice_Rec_1201708,Human_Splice_Rec_1201772,Human_Splice_Rec_1201838,Human_Splice_Rec_1201950,Human_Splice_Rec_1201988,Human_Splice_Rec_1202010,Human_Splice_Rec_1202020,Human_Splice_Rec_1202032 RMVar_hsa_circ_147634,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_20849,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_119513,RMVar_hsa_circ_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147663,RMVar_hsa_circ_147662,RMVar_hsa_circ_147660,RMVar_hsa_circ_326676,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_42290,RMVar_hsa_circ_77363,RMVar_hsa_circ_147672,RMVar_hsa_circ_29221,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_67602,RMVar_hsa_circ_147679,RMVar_hsa_circ_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_74924,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,RMVar_hsa_circ_363784,RMVar_hsa_circ_373076,RMVar_hsa_circ_285181,RMVar_hsa_circ_120713,RMVar_hsa_circ_50468,RMVar_hsa_circ_147683,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_330626,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_302654,RMVar_hsa_circ_147686,RMVar_hsa_circ_276230,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_15224,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147688,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147689,RMVar_hsa_circ_332588,RMVar_hsa_circ_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,RMVar_hsa_circ_147695,RMVar_hsa_circ_309285,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_271708,RMVar_hsa_circ_95967,RMVar_hsa_circ_147698,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_44012,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_147700,RMVar_hsa_circ_147701,RMVar_hsa_circ_147699,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_273538,RMVar_hsa_circ_91945,RMVar_hsa_circ_147709,RMVar_hsa_circ_28911,RMVar_hsa_circ_147710,RMVar_hsa_circ_147708 58072 RMVar_ID_58072 Human_SNP_ID_453935601 m1A Human chr11 - 3797486 3797486 3797486 GGTCGGTGGCAGGGGTGGTAGCGGCGGCGGCGACGGTTTCGTGGGGGCCGCGCGCTGCTCTGTGA GGTCGGTGGCAGGGGTGGTAGCGGCGGCGGCGTCGGTTTCGTGGGGGCCGCGCGCTGCTCTGTGA T A NUP98 Ensembl:ENSG00000110713 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3797359..3797550 26863196 MeRIP-seq:(Medium) rs1029231712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226441,Human_RBP_ID_749341,Human_RBP_ID_808435,Human_RBP_ID_4183917,Human_RBP_ID_8773980,Human_RBP_ID_17795738 Human_Splice_Rec_1201621,Human_Splice_Rec_1201685,Human_Splice_Rec_1201749,Human_Splice_Rec_1201815,Human_Splice_Rec_1201927,Human_Splice_Rec_1201965,Human_Splice_Rec_1202037 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 58073 RMVar_ID_58073 Human_SNP_ID_453935602 m1A Human chr11 - 3797486 3797486 3797486 GGTCGGTGGCAGGGGTGGTAGCGGCGGCGGCGACGGTTTCGTGGGGGCCGCGCGCTGCTCTGTGA GGTCGGTGGCAGGGGTGGTAGCGGCGGCGGCGGCGGTTTCGTGGGGGCCGCGCGCTGCTCTGTGA T C NUP98 Ensembl:ENSG00000110713 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3797359..3797550 26863196 MeRIP-seq:(Medium) rs1029231712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226441,Human_RBP_ID_749341,Human_RBP_ID_808435,Human_RBP_ID_4183917,Human_RBP_ID_8773980,Human_RBP_ID_17795738 Human_Splice_Rec_1201621,Human_Splice_Rec_1201685,Human_Splice_Rec_1201749,Human_Splice_Rec_1201815,Human_Splice_Rec_1201927,Human_Splice_Rec_1201965,Human_Splice_Rec_1202037 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 58074 RMVar_ID_58074 Human_SNP_ID_453935612 m1A Human chr11 - 3797499 3797499 3797499 CGCCCGAAGCGGCGGTCGGTGGCAGGGGTGGTAGCGGCGGCGGCGACGGTTTCGTGGGGGCCGCG CGCCCGAAGCGGCGGTCGGTGGCAGGGGTGGTGGCGGCGGCGGCGACGGTTTCGTGGGGGCCGCG T C NUP98 Ensembl:ENSG00000110713 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3797402..3797550 26863196 MeRIP-seq:(Medium) rs1564954457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30060,Human_RBP_ID_226441,Human_RBP_ID_749341,Human_RBP_ID_4184610,Human_RBP_ID_5460314,Human_RBP_ID_8773980 Human_Splice_Rec_1201621,Human_Splice_Rec_1201685,Human_Splice_Rec_1201749,Human_Splice_Rec_1201815,Human_Splice_Rec_1201927,Human_Splice_Rec_1201965,Human_Splice_Rec_1202037 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 58075 RMVar_ID_58075 Human_SNP_ID_453935634 m1A Human chr11 - 3797524 3797524 3797524 ACGCAGTCGGGCCCTCTGCGCGCTGCGCCCGAAGCGGCGGTCGGTGGCAGGGGTGGTAGCGGCGG ACGCAGTCGGGCCCTCTGCGCGCTGCGCCCGAGGCGGCGGTCGGTGGCAGGGGTGGTAGCGGCGG T C NUP98 Ensembl:ENSG00000110713 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:3797476..3797550 26863196 MeRIP-seq:(Medium) rs971748882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30060,Human_RBP_ID_4159626,Human_RBP_ID_8773981,Human_RBP_ID_18432696 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 58076 RMVar_ID_58076 Human_SNP_ID_453935635 m1A Human chr11 - 3797524 3797524 3797524 ACGCAGTCGGGCCCTCTGCGCGCTGCGCCCGAAGCGGCGGTCGGTGGCAGGGGTGGTAGCGGCGG ACGCAGTCGGGCCCTCTGCGCGCTGCGCCCGACGCGGCGGTCGGTGGCAGGGGTGGTAGCGGCGG T G NUP98 Ensembl:ENSG00000110713 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:3797476..3797550 26863196 MeRIP-seq:(Medium) rs971748882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30060,Human_RBP_ID_4159626,Human_RBP_ID_8773981,Human_RBP_ID_18432696 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 58077 RMVar_ID_58077 Human_SNP_ID_453935864 m1A Human chr11 - 3797956 3797952 3797956 AGTTACCATGCCATTCTGGGGCCGTCCCTCTGATTGGCCCGAGCTCCCTCAGCCCGAGTCGCGGC AGTTACCATGCCATTCTGGGGCCGTCCCTCTG____GCCCGAGCTCCCTCAGCCCGAGTCGCGGC CCAAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3797746..3798034 26863196 MeRIP-seq:(Medium) rs1564957716 Functional Loss DEL dbSNP153 33..36 33 - - - 58078 RMVar_ID_58078 Human_SNP_ID_453935865 m1A Human chr11 + 3797964 3797964 3797964 TCGGGCTGAGGGAGCTCGGGCCAATCAGAGGGACGGCCCCAGAATGGCATGGTAACTATTCGACC TCGGGCTGAGGGAGCTCGGGCCAATCAGAGGGCCGGCCCCAGAATGGCATGGTAACTATTCGACC A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3797739..3798023 26863196 MeRIP-seq:(Medium) rs757468946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202059,Human_Splice_Rec_1202071,Human_Splice_Rec_1202083,Human_Splice_Rec_1202091,Human_Splice_Rec_1202101,Human_Splice_Rec_1202105,Human_Splice_Rec_1202115,Human_Splice_Rec_1202127,Human_Splice_Rec_1202135,Human_Splice_Rec_1202145,Human_Splice_Rec_1202157,Human_Splice_Rec_1202167,Human_Splice_Rec_1202181,Human_Splice_Rec_1202191,Human_Splice_Rec_1202197,Human_Splice_Rec_1202219 58079 RMVar_ID_58079 Human_SNP_ID_453935866 m1A Human chr11 + 3797964 3797964 3797964 TCGGGCTGAGGGAGCTCGGGCCAATCAGAGGGACGGCCCCAGAATGGCATGGTAACTATTCGACC TCGGGCTGAGGGAGCTCGGGCCAATCAGAGGGGCGGCCCCAGAATGGCATGGTAACTATTCGACC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3797739..3798023 26863196 MeRIP-seq:(Medium) rs757468946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202059,Human_Splice_Rec_1202071,Human_Splice_Rec_1202083,Human_Splice_Rec_1202091,Human_Splice_Rec_1202101,Human_Splice_Rec_1202105,Human_Splice_Rec_1202115,Human_Splice_Rec_1202127,Human_Splice_Rec_1202135,Human_Splice_Rec_1202145,Human_Splice_Rec_1202157,Human_Splice_Rec_1202167,Human_Splice_Rec_1202181,Human_Splice_Rec_1202191,Human_Splice_Rec_1202197,Human_Splice_Rec_1202219 58080 RMVar_ID_58080 Human_SNP_ID_453939043 m1A Human chr11 - 3808621 3808621 3808621 ACCCACGCGGTGGTGGCGAGAGTGCCGGCGGAACCCGGGGGCCCAGGTGGCCCGGGGTCGGGGGC ACCCACGCGGTGGTGGCGAGAGTGCCGGCGGAGCCCGGGGGCCCAGGTGGCCCGGGGTCGGGGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3808575..3808730 26863196 MeRIP-seq:(Medium) rs1367127094 Functional Loss SNV dbSNP153 33..33 33 - - - 58081 RMVar_ID_58081 Human_SNP_ID_453939044 m1A Human chr11 - 3808622 3808622 3808622 CACCCACGCGGTGGTGGCGAGAGTGCCGGCGGAACCCGGGGGCCCAGGTGGCCCGGGGTCGGGGG CACCCACGCGGTGGTGGCGAGAGTGCCGGCGGCACCCGGGGGCCCAGGTGGCCCGGGGTCGGGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:3808576..3808675;chr11:3808576..3808625 26863196 MeRIP-seq:(Medium) rs945841258 Functional Loss SNV dbSNP153 33..33 33 - - - 58082 RMVar_ID_58082 Human_SNP_ID_453939476 m1A Human chr11 - 3810733 3810733 3810733 CTTCAGTCCCTTCCCAGGCTCTGTGTGCCTGCACCGCAGTCCACAGTGGCAGGGATTCCATGGAA CTTCAGTCCCTTCCCAGGCTCTGTGTGCCTGCGCCGCAGTCCACAGTGGCAGGGATTCCATGGAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3810727..3810875 26863196 MeRIP-seq:(Medium) rs1234994000 Functional Loss SNV dbSNP153 33..33 33 - - - 58083 RMVar_ID_58083 Human_SNP_ID_453939866 m1A Human chr11 + 3812492 3812492 3812492 CCTGCTCCTTCCCAGGGCTAGTGTAGAGCTCTAGGTAGAAGAAGGATAGGAAGGTAGTTTAGGGA CCTGCTCCTTCCCAGGGCTAGTGTAGAGCTCTCGGTAGAAGAAGGATAGGAAGGTAGTTTAGGGA A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3812489..3812599 26863196 MeRIP-seq:(Medium) rs1384226339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23504578 58084 RMVar_ID_58084 Human_SNP_ID_453941325 m1A Human chr11 + 3817675 3817675 3817675 ACAAGGGGATGGGGGAAGGGTAGGTAAGTCAGAGTCAGAGATAATTCATGGGGGGAGACTCAGAG ACAAGGGGATGGGGGAAGGGTAGGTAAGTCAGGGTCAGAGATAATTCATGGGGGGAGACTCAGAG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3817563..3817776 26863196 MeRIP-seq:(Medium) rs1386965717 Functional Loss SNV dbSNP153 33..33 33 - - - 58085 RMVar_ID_58085 Human_SNP_ID_453941589 m1A Human chr11 + 3818329 3818326 3818329 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAAAAAAAAAAAAAAAACAATAACAGTGCAAGGGA GCAGAGGTTGCAGTGAGCCAAGATCGTGCC___AAAAAAAAAAAAAACAATAACAGTGCAAGGGA CAAA C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3818276..3818525 26863196 MeRIP-seq:(Medium) rs5789309 Functional Loss DEL dbSNP153 31..33 33 - - - 58086 RMVar_ID_58086 Human_SNP_ID_453941590 m1A Human chr11 + 3818329 3818326 3818329 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAAAAAAAAAAAAAAAACAATAACAGTGCAAGGGA GCAGAGGTTGCAGTGAGCCAAGATCGTGCCA__AAAAAAAAAAAAAACAATAACAGTGCAAGGGA CAAA CA PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3818276..3818525 26863196 MeRIP-seq:(Medium) rs5789309 Functional Loss DEL dbSNP153 32..33 33 - - - 58087 RMVar_ID_58087 Human_SNP_ID_453941591 m1A Human chr11 + 3818329 3818326 3818329 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAAAAAAAAAAAAAAAACAATAACAGTGCAAGGGA GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAA_AAAAAAAAAAAAAACAATAACAGTGCAAGGGA CAAA CAA PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3818276..3818525 26863196 MeRIP-seq:(Medium) rs5789309 Functional Loss DEL dbSNP153 33..33 33 - - - 58088 RMVar_ID_58088 Human_SNP_ID_453941595 m1A Human chr11 + 3818329 3818329 3818329 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAAAAAAAAAAAAAAAACAATAACAGTGCAAGGGA GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAACAAAAAAAAAAAAAACAATAACAGTGCAAGGGA A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3818276..3818525 26863196 MeRIP-seq:(Medium) rs75818904 Functional Loss SNV dbSNP153 33..33 33 - - - 58089 RMVar_ID_58089 Human_SNP_ID_453941596 m1A Human chr11 + 3818329 3818329 3818329 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAAAAAAAAAAAAAAAACAATAACAGTGCAAGGGA GCAGAGGTTGCAGTGAGCCAAGATCGTGCCAAGAAAAAAAAAAAAAACAATAACAGTGCAAGGGA A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3818276..3818525 26863196 MeRIP-seq:(Medium) rs75818904 Functional Loss SNV dbSNP153 33..33 33 - - - 58090 RMVar_ID_58090 Human_SNP_ID_453943191 m1A Human chr11 + 3824013 3824013 3824013 CTTCTTGGTGGCCTTCGCCTACTGGAACCACTACCTCAGCTGCACCTCCCCGTGTTCCTGCTATC CTTCTTGGTGGCCTTCGCCTACTGGAACCACTGCCTCAGCTGCACCTCCCCGTGTTCCTGCTATC A G PGAP2 Ensembl:ENSG00000148985 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3823963..3824084 26863196 MeRIP-seq:(Medium) rs879255232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8351255,Human_RBP_ID_17349967 Human_miRNA_ID_640,Human_miRNA_ID_4289,Human_miRNA_ID_7968,Human_miRNA_ID_11506,Human_miRNA_ID_15051,Human_miRNA_ID_18719,Human_miRNA_ID_22349,Human_miRNA_ID_25996,Human_miRNA_ID_282886,Human_miRNA_ID_490541,Human_miRNA_ID_493800,Human_miRNA_ID_1305669,Human_miRNA_ID_1914340,Human_miRNA_ID_1916791,Human_miRNA_ID_1919240,Human_miRNA_ID_1921697,Human_miRNA_ID_1924153,Human_miRNA_ID_1926605,Human_miRNA_ID_1929055,Human_miRNA_ID_1931508,Human_miRNA_ID_2012813,Human_miRNA_ID_2057846,Human_miRNA_ID_2168368,Human_miRNA_ID_2169891,Human_miRNA_ID_2629337,Human_miRNA_ID_2642448,Human_miRNA_ID_2759192,Human_miRNA_ID_3125189 Clinvar_Rec_174 GWAS_ID_6818 RMVar_hsa_circ_107193,RMVar_hsa_circ_147732 58091 RMVar_ID_58091 Human_SNP_ID_453943201 m1A Human chr11 + 3824043 3824043 3824043 CTACCTCAGCTGCACCTCCCCGTGTTCCTGCTATCGCCCGCTCTGCCGCCTCAACTTCGGCCTCA CTACCTCAGCTGCACCTCCCCGTGTTCCTGCTGTCGCCCGCTCTGCCGCCTCAACTTCGGCCTCA A G PGAP2 Ensembl:ENSG00000148985 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3823861..3824303 26863196 MeRIP-seq:(Medium) rs185342002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9321271,Human_RBP_ID_17349967 Human_Splice_Rec_1202053,Human_Splice_Rec_1202065,Human_Splice_Rec_1202077,Human_Splice_Rec_1202095,Human_Splice_Rec_1202121,Human_Splice_Rec_1202133,Human_Splice_Rec_1202139,Human_Splice_Rec_1202151,Human_Splice_Rec_1202161,Human_Splice_Rec_1202175,Human_Splice_Rec_1202217,Human_Splice_Rec_1202235,Human_Splice_Rec_1202249,Human_Splice_Rec_1202261,Human_Splice_Rec_1202281,Human_Splice_Rec_1202295,Human_Splice_Rec_1202305,Human_Splice_Rec_1202319,Human_Splice_Rec_1202325,Human_Splice_Rec_1202335,Human_Splice_Rec_1202343,Human_Splice_Rec_1202353,Human_Splice_Rec_1202369 Human_miRNA_ID_1183023 RMVar_hsa_circ_107193,RMVar_hsa_circ_147732 58092 RMVar_ID_58092 Human_SNP_ID_453943374 m1A Human chr11 - 3824502 3824502 3824502 TCAGTTTGTTCCCAAGCCCCAGCCCCAACCCCAGCACCCCTCTGCCAGGGTTCCCATTAGAACTC TCAGTTTGTTCCCAAGCCCCAGCCCCAACCCCGGCACCCCTCTGCCAGGGTTCCCATTAGAACTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:3824451..3824700 26863196 MeRIP-seq:(Medium) rs1361943850 Functional Loss SNV dbSNP153 33..33 33 - - - 58093 RMVar_ID_58093 Human_SNP_ID_453944196 m1A Human chr11 + 3827183 3827183 3827183 TGGGGGCGCAATTCCAAGAGCAGCGAGGGCAGAGGTTAGAGATGGCTGAGAGCCCCTAACCTGAG TGGGGGCGCAATTCCAAGAGCAGCGAGGGCAGCGGTTAGAGATGGCTGAGAGCCCCTAACCTGAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3827041..3827276 26863196 MeRIP-seq:(Medium) rs1565080171 Functional Loss SNV dbSNP153 33..33 33 - - - 58094 RMVar_ID_58094 Human_SNP_ID_453944197 m1A Human chr11 - 3827186 3827186 3827186 CGCCTCAGGTTAGGGGCTCTCAGCCATCTCTAACCTCTGCCCTCGCTGCTCTTGGAATTGCGCCC CGCCTCAGGTTAGGGGCTCTCAGCCATCTCTAGCCTCTGCCCTCGCTGCTCTTGGAATTGCGCCC T C RHOG Ensembl:ENSG00000177105 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:3827026..3827325 26863196 MeRIP-seq:(Medium) rs1246248572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396064,Human_RBP_ID_750550,Human_RBP_ID_5110348,Human_RBP_ID_17074095,Human_RBP_ID_17349970,Human_RBP_ID_18432697,Human_RBP_ID_22034205,Human_RBP_ID_27201292 Human_miRNA_ID_356305,Human_miRNA_ID_2252232,Human_miRNA_ID_2272773,Human_miRNA_ID_2438540,Human_miRNA_ID_2756586 RMVar_hsa_circ_83937,RMVar_hsa_circ_100703,RMVar_hsa_circ_147734,RMVar_hsa_circ_147735 58095 RMVar_ID_58095 Human_SNP_ID_453944198 m1A Human chr11 - 3827187 3827187 3827187 CCGCCTCAGGTTAGGGGCTCTCAGCCATCTCTAACCTCTGCCCTCGCTGCTCTTGGAATTGCGCC CCGCCTCAGGTTAGGGGCTCTCAGCCATCTCTGACCTCTGCCCTCGCTGCTCTTGGAATTGCGCC T C RHOG Ensembl:ENSG00000177105 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3827048..3827233 26863196 MeRIP-seq:(Medium) rs895120921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396064,Human_RBP_ID_750550,Human_RBP_ID_5110348,Human_RBP_ID_17074095,Human_RBP_ID_17349970,Human_RBP_ID_18432697,Human_RBP_ID_22034205,Human_RBP_ID_27201292 Human_miRNA_ID_356305,Human_miRNA_ID_2252232,Human_miRNA_ID_2272773,Human_miRNA_ID_2756586 RMVar_hsa_circ_83937,RMVar_hsa_circ_100703,RMVar_hsa_circ_147734,RMVar_hsa_circ_147735 58096 RMVar_ID_58096 Human_SNP_ID_453944200 m1A Human chr11 - 3827197 3827197 3827197 TATTGTGGTGCCGCCTCAGGTTAGGGGCTCTCAGCCATCTCTAACCTCTGCCCTCGCTGCTCTTG TATTGTGGTGCCGCCTCAGGTTAGGGGCTCTCGGCCATCTCTAACCTCTGCCCTCGCTGCTCTTG T C RHOG Ensembl:ENSG00000177105 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:3827096..3827285 26863196 MeRIP-seq:(Medium) rs1327196706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750550,Human_RBP_ID_4159672,Human_RBP_ID_5110348,Human_RBP_ID_5234957,Human_RBP_ID_17074095,Human_RBP_ID_17349970,Human_RBP_ID_22034205 Human_miRNA_ID_256719,Human_miRNA_ID_260511,Human_miRNA_ID_2272773 RMVar_hsa_circ_83937,RMVar_hsa_circ_100703,RMVar_hsa_circ_147734,RMVar_hsa_circ_147735 58097 RMVar_ID_58097 Human_SNP_ID_453948128 m1A Human chr11 - 3840921 3840921 3840921 TTCTCGAGCCCGGAGCCGCTGCCGCCGCCCCCAGCTCCCCCGCCTCGGGGAGGGCACCAGGTGAG TTCTCGAGCCCGGAGCCGCTGCCGCCGCCCCCGGCTCCCCCGCCTCGGGGAGGGCACCAGGTGAG T C RHOG Ensembl:ENSG00000177105 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3840790..3840950 26863196 MeRIP-seq:(Medium) rs935416779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750553,Human_RBP_ID_4183923 Human_Splice_Rec_1202373 RMVar_hsa_circ_100703,RMVar_hsa_circ_147735 58098 RMVar_ID_58098 Human_SNP_ID_453948141 m1A Human chr11 - 3840940 3840940 3840940 GCCTCCCGCTCTCACTTCCTTCTCGAGCCCGGAGCCGCTGCCGCCGCCCCCAGCTCCCCCGCCTC GCCTCCCGCTCTCACTTCCTTCTCGAGCCCGGGGCCGCTGCCGCCGCCCCCAGCTCCCCCGCCTC T C RHOG Ensembl:ENSG00000177105 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3840416..3840975 26863196 MeRIP-seq:(Medium) rs1181914726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184616,Human_RBP_ID_5489638 Human_Splice_Rec_1202373 RMVar_hsa_circ_100703,RMVar_hsa_circ_147735 58099 RMVar_ID_58099 Human_SNP_ID_453948262 m1A Human chr11 - 3841131 3841131 3841131 CTTGGGAGGCCTGACTTACTGACCGCAGGGGCAGCGGACTGGGAGGGGAACGTGGCAAGCCCGGG CTTGGGAGGCCTGACTTACTGACCGCAGGGGCGGCGGACTGGGAGGGGAACGTGGCAAGCCCGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:3841084..3841232 26863196 MeRIP-seq:(Medium) rs952837823 Functional Loss SNV dbSNP153 33..33 33 - - - 58100 RMVar_ID_58100 Human_SNP_ID_453951832 m1A Human chr11 - 3855258 3855258 3855258 TCCACTCGCCTCAGTTCTAGAGCTGTCTAAACAGAGGCCCAGGACACGACGTTAGCCTCCCAGGA TCCACTCGCCTCAGTTCTAGAGCTGTCTAAACGGAGGCCCAGGACACGACGTTAGCCTCCCAGGA T C AC090587.1 Ensembl:ENSG00000228661 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3855207..3855399 26863196 MeRIP-seq:(Medium) rs1173553272 Functional Loss SNV dbSNP153 33..33 33 - - - 58101 RMVar_ID_58101 Human_SNP_ID_453951870 m1A Human chr11 + 3855424 3855424 3855424 CCGCGGTTGGCGCTGGAGACTCTCGGTGGGGAAAGGGAAGCTGGGACTTGATCCTTTGCGCGGGA CCGCGGTTGGCGCTGGAGACTCTCGGTGGGGAGAGGGAAGCTGGGACTTGATCCTTTGCGCGGGA A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3855373..3855495 26863196 MeRIP-seq:(Medium) rs890158733 Functional Loss SNV dbSNP153 33..33 33 - - - 58102 RMVar_ID_58102 Human_SNP_ID_453964786 m1A Human chr11 - 3904699 3904699 3904699 TCACCTAACACTGCCTCCTTCATCCTTCCGTCACACAATTTAAATCAACCCCCATGACCACTACC TCACCTAACACTGCCTCCTTCATCCTTCCGTCCCACAATTTAAATCAACCCCCATGACCACTACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3904695..3904814 26863196 MeRIP-seq:(Medium) rs1259730696 Functional Loss SNV dbSNP153 33..33 33 - - - 58103 RMVar_ID_58103 Human_SNP_ID_453966560 m1A Human chr11 + 3912049 3912049 3912049 AGTTAAATAAGTAGGCTTTGTTGGTATTGTTCAGTCTAGTGAGGCTAATAGGGGGCATCTATCCA AGTTAAATAAGTAGGCTTTGTTGGTATTGTTCGGTCTAGTGAGGCTAATAGGGGGCATCTATCCA A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:3912039..3912127 26863196 MeRIP-seq:(Medium) rs1182505917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18933280 RMVar_hsa_circ_104299,RMVar_hsa_circ_147736 58104 RMVar_ID_58104 Human_SNP_ID_454006752 m1A Human chr11 + 4082294 4082294 4082294 TGGCTGCAGCTGACACATGAGGTGGAGGTGCAATATTACAACATCAAGAAGCAAAATGCTGAGAA TGGCTGCAGCTGACACATGAGGTGGAGGTGCAGTATTACAACATCAAGAAGCAAAATGCTGAGAA A G STIM1 Ensembl:ENSG00000167323 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4082244..4082347 26863196 MeRIP-seq:(Medium) rs2304891 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_987082,Human_RBP_ID_17795822 Human_Splice_Rec_1202405,Human_Splice_Rec_1202427,Human_Splice_Rec_1202449,Human_Splice_Rec_1202541,Human_Splice_Rec_1202551,Human_Splice_Rec_1202561 GWAS_ID_6819,GWAS_ID_6820,GWAS_ID_6821 RMVar_hsa_circ_104299,RMVar_hsa_circ_147736,RMVar_hsa_circ_84531,RMVar_hsa_circ_147747,RMVar_hsa_circ_119467,RMVar_hsa_circ_308319,RMVar_hsa_circ_99657,RMVar_hsa_circ_43338,RMVar_hsa_circ_147746,RMVar_hsa_circ_308029,RMVar_hsa_circ_147754,RMVar_hsa_circ_147755,RMVar_hsa_circ_340651,RMVar_hsa_circ_147759,RMVar_hsa_circ_80919,RMVar_hsa_circ_147758 58105 RMVar_ID_58105 Human_SNP_ID_454009931 m1A Human chr11 - 4094876 4094869 4094877 GCTGCTCAGGGGAAAGAACTGGAGTTGGAGCCAGACAGCACTTTCTTCAGAGCAGAGGCGCAACA GCTGCTCAGGGGAAAGAACTGGAGTTGGAGC________ACTTTCTTCAGAGCAGAGGCGCAACA TGCTGTCTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:4094801..4095190 26863196 MeRIP-seq:(Medium) rs1054628532 Functional Loss DEL dbSNP153 32..39 33 - - - 58106 RMVar_ID_58106 Human_SNP_ID_454009934 m1A Human chr11 - 4094876 4094876 4094876 GCTGCTCAGGGGAAAGAACTGGAGTTGGAGCCAGACAGCACTTTCTTCAGAGCAGAGGCGCAACA GCTGCTCAGGGGAAAGAACTGGAGTTGGAGCCGGACAGCACTTTCTTCAGAGCAGAGGCGCAACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:4094801..4095190 26863196 MeRIP-seq:(Medium) rs891927345 Functional Loss SNV dbSNP153 33..33 33 - - - 58107 RMVar_ID_58107 Human_SNP_ID_454009957 m1A Human chr11 + 4094938 4094938 4094938 AGCGCCTGGAACCTAACCCTTCCCACTCTGTCACCTTCTCGATCCCGCCGGCGCTTTAGAGCCGC AGCGCCTGGAACCTAACCCTTCCCACTCTGTCGCCTTCTCGATCCCGCCGGCGCTTTAGAGCCGC A G RRM1 Ensembl:ENSG00000167325 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:4094837..4094956 26863410 MeRIP-seq:(Medium) rs1291649251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226907,Human_RBP_ID_1161976,Human_RBP_ID_4159865,Human_RBP_ID_5415956,Human_RBP_ID_5436439,Human_RBP_ID_5460324,Human_RBP_ID_5489653,Human_RBP_ID_9321274,Human_RBP_ID_9361956,Human_RBP_ID_17349974,Human_RBP_ID_17795853,Human_RBP_ID_22035082,Human_RBP_ID_22161546,Human_RBP_ID_22432759,Human_RBP_ID_26803146 Human_Splice_Rec_1202575,Human_Splice_Rec_1202579,Human_Splice_Rec_1202617,Human_Splice_Rec_1202653,Human_Splice_Rec_1202659,Human_Splice_Rec_1202693 Human_miRNA_ID_2877405 RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 58108 RMVar_ID_58108 Human_SNP_ID_454010038 m1A Human chr11 + 4095105 4095104 4095105 TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGACCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAG_CCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT GA G RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:4095080..4095300 26863196 MeRIP-seq:(Medium) rs111548639 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 58109 RMVar_ID_58109 Human_SNP_ID_454010040 m1A Human chr11 + 4095105 4095105 4095105 TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGACCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGCCCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT A C RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:4095080..4095300 26863196 MeRIP-seq:(Medium) rs12801088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 58110 RMVar_ID_58110 Human_SNP_ID_454010041 m1A Human chr11 + 4095105 4095105 4095105 TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGACCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGTCCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT A T RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:4095080..4095300 26863196 MeRIP-seq:(Medium) rs12801088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 58111 RMVar_ID_58111 Human_SNP_ID_454011765 m1A Human chr11 + 4101936 4101936 4101936 CATGTTAATTACATTTGATTCTTTGACATTGTAGTCTTAATAATTGCTAACATGAATTTAATAAT CATGTTAATTACATTTGATTCTTTGACATTGTTGTCTTAATAATTGCTAACATGAATTTAATAAT A T RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:4101933..4102005 26863196 MeRIP-seq:(Medium) rs1415767297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 58112 RMVar_ID_58112 Human_SNP_ID_454016929 m1A Human chr11 + 4123383 4123383 4123383 CACAGAAATAGTGGAGTACACCAGCAAAGATGAGGTAGGTAGAAAAAATTCTTCCTAGAGTACTA CACAGAAATAGTGGAGTACACCAGCAAAGATGGGGTAGGTAGAAAAAATTCTTCCTAGAGTACTA A G RRM1 Ensembl:ENSG00000167325 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4123361..4126760 32194978 MeRIP-seq:(Medium) rs1249997322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17804895 Human_Splice_Rec_1202603,Human_Splice_Rec_1202639,Human_Splice_Rec_1202679,Human_Splice_Rec_1202721,Human_Splice_Rec_1202745,Human_Splice_Rec_1202783,Human_Splice_Rec_1202787 RMVar_hsa_circ_341423,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_369290,RMVar_hsa_circ_147772,RMVar_hsa_circ_55496,RMVar_hsa_circ_316394,RMVar_hsa_circ_51885,RMVar_hsa_circ_24516,RMVar_hsa_circ_28571,RMVar_hsa_circ_29090,RMVar_hsa_circ_90550,RMVar_hsa_circ_124542,RMVar_hsa_circ_147775,RMVar_hsa_circ_147776,RMVar_hsa_circ_45312,RMVar_hsa_circ_269177,RMVar_hsa_circ_28819,RMVar_hsa_circ_29685,RMVar_hsa_circ_147777 58113 RMVar_ID_58113 Human_SNP_ID_454020843 m1A Human chr11 + 4138278 4138278 4138278 ATCCAGTTCACTCTAAATAAGGAGAAGCTAAAAGATAAAGAAAAGGTATCAAAAGAGGAAGAAGA ATCCAGTTCACTCTAAATAAGGAGAAGCTAAAGGATAAAGAAAAGGTATCAAAAGAGGAAGAAGA A G RRM1 Ensembl:ENSG00000167325 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4138229..4138429 32194978 MeRIP-seq:(Medium) rs1409588853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26318042 Human_Splice_Rec_1202616,Human_Splice_Rec_1202652,Human_Splice_Rec_1202692,Human_Splice_Rec_1202734,Human_Splice_Rec_1202758 RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_90550,RMVar_hsa_circ_124542,RMVar_hsa_circ_147776,RMVar_hsa_circ_147777,RMVar_hsa_circ_80818,RMVar_hsa_circ_147778 58114 RMVar_ID_58114 Human_SNP_ID_454020850 m1A Human chr11 + 4138299 4138299 4138299 GAGAAGCTAAAAGATAAAGAAAAGGTATCAAAAGAGGAAGAAGAGAAGGAGAGGAACACAGCAGC GAGAAGCTAAAAGATAAAGAAAAGGTATCAAAGGAGGAAGAAGAGAAGGAGAGGAACACAGCAGC A G RRM1 Ensembl:ENSG00000167325 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4138248..4138456 26863196 MeRIP-seq:(Medium) rs763906229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4190308,Human_RBP_ID_8351321,Human_RBP_ID_26318042 Human_miRNA_ID_3117661 RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_90550,RMVar_hsa_circ_124542,RMVar_hsa_circ_147776,RMVar_hsa_circ_147777,RMVar_hsa_circ_80818,RMVar_hsa_circ_147778 58115 RMVar_ID_58115 Human_SNP_ID_454107934 m1A Human chr11 - 4388457 4388455 4388458 TGTGCAGCAAAAAAACTTCCTGGTTGAAGAAGAACAGAGGCAGCTGCAGGAGCTGGAGAAGGATG TGTGCAGCAAAAAAACTTCCTGGTTGAAGAA___CAGAGGCAGCTGCAGGAGCTGGAGAAGGATG GTTC G TRIM21 Ensembl:ENSG00000132109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4388408..4388489 26863196 MeRIP-seq:(Medium) rs1299357362 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1202810 RMVar_hsa_circ_60388 58116 RMVar_ID_58116 Human_SNP_ID_454107936 m1A Human chr11 - 4388457 4388457 4388457 TGTGCAGCAAAAAAACTTCCTGGTTGAAGAAGAACAGAGGCAGCTGCAGGAGCTGGAGAAGGATG TGTGCAGCAAAAAAACTTCCTGGTTGAAGAAGCACAGAGGCAGCTGCAGGAGCTGGAGAAGGATG T G TRIM21 Ensembl:ENSG00000132109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4388408..4388489 26863196 MeRIP-seq:(Medium) rs1403178097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202810 RMVar_hsa_circ_60388 58117 RMVar_ID_58117 Human_SNP_ID_454108334 m1A Human chr11 - 4389713 4389713 4389713 AGCTCCAGGTGGCATTAGGGGAACTGAGAAGAAAGCAGGAGTTGGCTGAGAAGTTGGAAGTGGAA AGCTCCAGGTGGCATTAGGGGAACTGAGAAGAGAGCAGGAGTTGGCTGAGAAGTTGGAAGTGGAA T C TRIM21 Ensembl:ENSG00000132109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4389635..4389766 26863196 MeRIP-seq:(Medium) rs745654190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202808,Human_Splice_Rec_1202809 RMVar_hsa_circ_60388 58118 RMVar_ID_58118 Human_SNP_ID_454108624 m1A Human chr11 - 4390401 4390401 4390401 TGCTGTTTAACGGCACACTTGACAATGGCTTCAGCAGCACGCTTGACAATGATGTGGGAGGAGGT TGCTGTTTAACGGCACACTTGACAATGGCTTCGGCAGCACGCTTGACAATGATGTGGGAGGAGGT T C TRIM21 Ensembl:ENSG00000132109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4390351..4390428 26863196 MeRIP-seq:(Medium) rs1394250777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202806 58119 RMVar_ID_58119 Human_SNP_ID_454181088 m1A Human chr11 + 4599863 4599863 4599863 AGCTCTGGGTATGCGCAGCATTTTTTTGGCCTATTGGGAAAGCCCATCTAATGGTGTCCTGAAGA AGCTCTGGGTATGCGCAGCATTTTTTTGGCCTGTTGGGAAAGCCCATCTAATGGTGTCCTGAAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4599816..4599916 32194978 MeRIP-seq:(Medium) rs138145498 Functional Loss SNV dbSNP153 33..33 33 - - - 58120 RMVar_ID_58120 Human_SNP_ID_454181150 m1A Human chr11 + 4600116 4600112 4600116 CCTCTGCTTTTTAAAATAAGTGGTTTCATGACAGACTTCAGCCTGGTAGCAAAGACCAAAGGATC CCTCTGCTTTTTAAAATAAGTGGTTTCAT____GACTTCAGCCTGGTAGCAAAGACCAAAGGATC TGACA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4600015..4600116 32194978 MeRIP-seq:(Medium) rs1454515043 Functional Loss DEL dbSNP153 30..33 33 - - - 58121 RMVar_ID_58121 Human_SNP_ID_454181152 m1A Human chr11 + 4600116 4600116 4600116 CCTCTGCTTTTTAAAATAAGTGGTTTCATGACAGACTTCAGCCTGGTAGCAAAGACCAAAGGATC CCTCTGCTTTTTAAAATAAGTGGTTTCATGACTGACTTCAGCCTGGTAGCAAAGACCAAAGGATC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4600015..4600116 32194978 MeRIP-seq:(Medium) rs894627869 Functional Loss SNV dbSNP153 33..33 33 - - - 58122 RMVar_ID_58122 Human_SNP_ID_454181362 m1A Human chr11 - 4600604 4600604 4600604 CAGGTCTGAGTGGGGCCTGGGAGTATGTAAGCAAAATGTAGACCGGAAGGAGGTGGTCTACTTAT CAGGTCTGAGTGGGGCCTGGGAGTATGTAAGCCAAATGTAGACCGGAAGGAGGTGGTCTACTTAT T G TRIM68 Ensembl:ENSG00000167333 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:4600554..4600667 26863196 MeRIP-seq:(Medium) rs1299104700 Functional Loss SNV dbSNP153 33..33 33 - - - 58123 RMVar_ID_58123 Human_SNP_ID_454181366 m1A Human chr11 - 4600612 4600612 4600612 GTGGGAGACAGGTCTGAGTGGGGCCTGGGAGTATGTAAGCAAAATGTAGACCGGAAGGAGGTGGT GTGGGAGACAGGTCTGAGTGGGGCCTGGGAGTCTGTAAGCAAAATGTAGACCGGAAGGAGGTGGT T G TRIM68 Ensembl:ENSG00000167333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:4600506..4600671 26863196 MeRIP-seq:(Medium) rs375151620 Functional Loss SNV dbSNP153 33..33 33 - - - 58124 RMVar_ID_58124 Human_SNP_ID_454181569 m1A Human chr11 + 4601111 4601111 4601111 CAACTCCAGGGAGATTGGTTCTGGCTGCTGCAAGCTCCAAGATTTGCTCCTGGTAGAGGAGGGTG CAACTCCAGGGAGATTGGTTCTGGCTGCTGCAGGCTCCAAGATTTGCTCCTGGTAGAGGAGGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:4601061..4601162 32194978 MeRIP-seq:(Medium) rs748816001 Functional Loss SNV dbSNP153 33..33 33 - - - 58125 RMVar_ID_58125 Human_SNP_ID_454181942 m1A Human chr11 - 4602314 4602314 4602314 AAAAAGCAGCCACCACATCGGCAGCTGGGGGCAGAGGTAGCAGCAGCTCTGGCCAGCCTACAGCG AAAAAGCAGCCACCACATCGGCAGCTGGGGGCGGAGGTAGCAGCAGCTCTGGCCAGCCTACAGCG T C TRIM68 Ensembl:ENSG00000167333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4602268..4602397 26863196 MeRIP-seq:(Medium) rs139418325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202852,Human_Splice_Rec_1202880 RMVar_hsa_circ_47436 58126 RMVar_ID_58126 Human_SNP_ID_454181956 m1A Human chr11 - 4602339 4602339 4602339 TGAAAAATACCAGCGATTACTAGAGAAAAAGCAGCCACCACATCGGCAGCTGGGGGCAGAGGTAG TGAAAAATACCAGCGATTACTAGAGAAAAAGCGGCCACCACATCGGCAGCTGGGGGCAGAGGTAG T C TRIM68 Ensembl:ENSG00000167333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:4602290..4602421 26863196 MeRIP-seq:(Medium) rs552545459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1202852,Human_Splice_Rec_1202880 Human_miRNA_ID_732366 RMVar_hsa_circ_47436 58127 RMVar_ID_58127 Human_SNP_ID_454627471 m1A Human chr11 - 6212195 6212195 6212195 GGGCATGGAGAAGGAATGGATCTTAACTGGGAATGAAGTGGCTAAAGTGTTGATTGATTAAGACT GGGCATGGAGAAGGAATGGATCTTAACTGGGATTGAAGTGGCTAAAGTGTTGATTGATTAAGACT T A FAM160A2 Ensembl:ENSG00000051009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6212148..6212520 26863196 MeRIP-seq:(Medium) rs776359835 Functional Loss SNV dbSNP153 33..33 33 - - - 58128 RMVar_ID_58128 Human_SNP_ID_454627475 m1A Human chr11 - 6212219 6212219 6212219 ATAGGAGAATTCGTCAGGGTGAGAGGGCATGGAGAAGGAATGGATCTTAACTGGGAATGAAGTGG ATAGGAGAATTCGTCAGGGTGAGAGGGCATGGGGAAGGAATGGATCTTAACTGGGAATGAAGTGG T C FAM160A2 Ensembl:ENSG00000051009 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:6212186..6212317 26863196 MeRIP-seq:(Medium) rs1445037664 Functional Loss SNV dbSNP153 33..33 33 - - - 58129 RMVar_ID_58129 Human_SNP_ID_454628998 m1A Human chr11 - 6217609 6217609 6217609 GTTCGTCTGGTGCCAAAGGAGGGAGCTGGGGAACTGCTAGAGGGCATCTCCGAGGGCATGGCAGG GTTCGTCTGGTGCCAAAGGAGGGAGCTGGGGAGCTGCTAGAGGGCATCTCCGAGGGCATGGCAGG T C FAM160A2 Ensembl:ENSG00000051009 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:6217558..6217714 26863196 MeRIP-seq:(Medium) rs1204876035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3938886,Human_RBP_ID_5314087,Human_RBP_ID_8174133,Human_RBP_ID_9414083 Human_miRNA_ID_1968565,Human_miRNA_ID_2257503 RMVar_hsa_circ_61084,RMVar_hsa_circ_97259,RMVar_hsa_circ_122299,RMVar_hsa_circ_147813,RMVar_hsa_circ_147814 58130 RMVar_ID_58130 Human_SNP_ID_454633375 m1A Human chr11 - 6234067 6234067 6234067 AGGCCTCCTTCGATGGACTGCCCTGTCCAGTGAGAGCAATAGTTTTAGACAAAGTAGGGCAGCTT AGGCCTCCTTCGATGGACTGCCCTGTCCAGTGGGAGCAATAGTTTTAGACAAAGTAGGGCAGCTT T C FAM160A2 Ensembl:ENSG00000051009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6234065..6234558 26863196 MeRIP-seq:(Medium) rs1055517476 Functional Loss SNV dbSNP153 33..33 33 - - - 58131 RMVar_ID_58131 Human_SNP_ID_454633509 m1A Human chr11 - 6234568 6234568 6234568 ACCTAACACCGCAGCAGCAACCGGGCCCGGCCAGGTTCGGCGTTCCGTGAGTGAACGGTACGCAT ACCTAACACCGCAGCAGCAACCGGGCCCGGCCGGGTTCGGCGTTCCGTGAGTGAACGGTACGCAT T C FAM160A2 Ensembl:ENSG00000051009 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:6234105..6234579 26863196 MeRIP-seq:(Medium) rs1370304324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1203599,Human_Splice_Rec_1203621,Human_Splice_Rec_1203643 58132 RMVar_ID_58132 Human_SNP_ID_454655467 m1A Human chr11 - 6319176 6319176 6319176 TGGGGCTGCCGAAGAAGCTCTGCTCCAAATGGAGAGTGTAGCCTGAGGGCTGGTGTTGCCTGCCT TGGGGCTGCCGAAGAAGCTCTGCTCCAAATGGGGAGTGTAGCCTGAGGGCTGGTGTTGCCTGCCT T C CAVIN3 Ensembl:ENSG00000170955 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6319126..6319683 32194978 MeRIP-seq:(Medium) rs762061933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2047621 RMVar_hsa_circ_103803,RMVar_hsa_circ_126440,RMVar_hsa_circ_147817,RMVar_hsa_circ_147818 58133 RMVar_ID_58133 Human_SNP_ID_454655585 m1A Human chr11 + 6319383 6319383 6319383 CAGGGCCTTTCCGGCCCGAAAGGGCCCTTCGGAGGCTCTGTACCTTCTGCAATCCGGTGCGCCGC CAGGGCCTTTCCGGCCCGAAAGGGCCCTTCGGCGGCTCTGTACCTTCTGCAATCCGGTGCGCCGC A C AC068733.3 Ensembl:ENSG00000282556 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:6319333..6319476 26863196 MeRIP-seq:(Medium) rs765898204 Functional Loss SNV dbSNP153 33..33 33 - - - 58134 RMVar_ID_58134 Human_SNP_ID_454656134 m1A Human chr11 - 6320457 6320457 6320457 GCGGTCAGGGATCATGAGGGAGAGTGCGTTGGAGCGGGGGCCTGTGCCCGAGGCGCCGGCGGGGG GCGGTCAGGGATCATGAGGGAGAGTGCGTTGGGGCGGGGGCCTGTGCCCGAGGCGCCGGCGGGGG T C CAVIN3 Ensembl:ENSG00000170955 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:6320076..6320550;chr11:6320126..6320550;chr11:6320151..6320525 26863196 MeRIP-seq:(Medium) rs748407762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126440,RMVar_hsa_circ_147817 58135 RMVar_ID_58135 Human_SNP_ID_454678137 m1A Human chr11 - 6403770 6403770 6403770 GCCTTCGAGACGGATTCCGACCTGCCGGCTGGATGGATGAGGGTCCAGGACACCTCAGGGACCTA GCCTTCGAGACGGATTCCGACCTGCCGGCTGGGTGGATGAGGGTCCAGGACACCTCAGGGACCTA T C APBB1 Ensembl:ENSG00000166313 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6403658..6403859 32194978 MeRIP-seq:(Medium) rs143407326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400010 Human_Splice_Rec_1203836,Human_Splice_Rec_1203856,Human_Splice_Rec_1203878,Human_Splice_Rec_1203900,Human_Splice_Rec_1203924,Human_Splice_Rec_1203948,Human_Splice_Rec_1203974,Human_Splice_Rec_1203998,Human_Splice_Rec_1204024,Human_Splice_Rec_1204050,Human_Splice_Rec_1204074,Human_Splice_Rec_1204126,Human_Splice_Rec_1204150,Human_Splice_Rec_1204174,Human_Splice_Rec_1204196,Human_Splice_Rec_1204214,Human_Splice_Rec_1204246,Human_Splice_Rec_1204260,Human_Splice_Rec_1204272 Human_miRNA_ID_2509255 RMVar_hsa_circ_10278,RMVar_hsa_circ_147826,RMVar_hsa_circ_320574,RMVar_hsa_circ_331319,RMVar_hsa_circ_45787 58136 RMVar_ID_58136 Human_SNP_ID_454682275 m1A Human chr11 - 6419306 6419306 6419306 TGTGGAATAGTAGTGGAGGACGGCGCCGCGCTAGGCGGGGGTCCCAGGGAGTCGGCTGCAGGGGT TGTGGAATAGTAGTGGAGGACGGCGCCGCGCTGGGCGGGGGTCCCAGGGAGTCGGCTGCAGGGGT T C APBB1 Ensembl:ENSG00000166313 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6419297..6419401 26863196 MeRIP-seq:(Medium) rs1026386706 Functional Loss SNV dbSNP153 33..33 33 - - - 58137 RMVar_ID_58137 Human_SNP_ID_454690062 m1A Human chr11 - 6450128 6450128 6450128 GGACGAGAGTGTTTGAGACAAAAGACACAGGAAGAGCCAAGAATGCAAGGTGGGAACCTTAATAG GGACGAGAGTGTTTGAGACAAAAGACACAGGAGGAGCCAAGAATGCAAGGTGGGAACCTTAATAG T C TRIM3 Ensembl:ENSG00000110171 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6450078..6450242 26863196 MeRIP-seq:(Medium) rs1377275692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2274819,Human_RBP_ID_11668606 58138 RMVar_ID_58138 Human_SNP_ID_454697156 m1A Human chr11 - 6477812 6477812 6477812 CCCCCGGGATGCAGGGACACGTGGTCGACTTGAGAGTGCCCAGGCCACTTTCCAGGCCCATCGGG CCCCCGGGATGCAGGGACACGTGGTCGACTTGGGAGTGCCCAGGCCACTTTCCAGGCCCATCGGG T C ARFIP2 Ensembl:ENSG00000132254 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6477762..6477862 32194978 MeRIP-seq:(Medium) rs1364301140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226505,Human_RBP_ID_400454,Human_RBP_ID_807954,Human_RBP_ID_9276233,Human_RBP_ID_17804436,Human_RBP_ID_22035093,Human_RBP_ID_22570581,Human_RBP_ID_26318047,Human_RBP_ID_27204532 Human_Splice_Rec_1204532,Human_Splice_Rec_1204533,Human_Splice_Rec_1204546,Human_Splice_Rec_1204547,Human_Splice_Rec_1204560,Human_Splice_Rec_1204561,Human_Splice_Rec_1204574,Human_Splice_Rec_1204575,Human_Splice_Rec_1204584,Human_Splice_Rec_1204585,Human_Splice_Rec_1204596,Human_Splice_Rec_1204597 Human_miRNA_ID_2781295,Human_miRNA_ID_2786862 RMVar_hsa_circ_28375,RMVar_hsa_circ_56624,RMVar_hsa_circ_107460,RMVar_hsa_circ_147828 58139 RMVar_ID_58139 Human_SNP_ID_454697969 m1A Human chr11 - 6480391 6480391 6480391 CCATGACGGACGGGATCCTAGGGAAGGCAGCCACAATGGAGATCCCTATCCACGGGAACGGCGAA CCATGACGGACGGGATCCTAGGGAAGGCAGCCGCAATGGAGATCCCTATCCACGGGAACGGCGAA T C ARFIP2 Ensembl:ENSG00000132254 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6480342..6480734 32194978 MeRIP-seq:(Medium) rs1411487165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870220,Human_RBP_ID_4184626,Human_RBP_ID_6084924,Human_RBP_ID_22895275,Human_RBP_ID_24913240 Human_Splice_Rec_1204522,Human_Splice_Rec_1204523,Human_Splice_Rec_1204536,Human_Splice_Rec_1204537,Human_Splice_Rec_1204550,Human_Splice_Rec_1204551,Human_Splice_Rec_1204564,Human_Splice_Rec_1204565,Human_Splice_Rec_1204600,Human_Splice_Rec_1204601,Human_Splice_Rec_1204612,Human_Splice_Rec_1204613,Human_Splice_Rec_1204616 Human_miRNA_ID_2047622 RMVar_hsa_circ_147830,RMVar_hsa_circ_90002 58140 RMVar_ID_58140 Human_SNP_ID_454697972 m1A Human chr11 - 6480404 6480404 6480404 ATACCTTTCCTAGCCATGACGGACGGGATCCTAGGGAAGGCAGCCACAATGGAGATCCCTATCCA ATACCTTTCCTAGCCATGACGGACGGGATCCTGGGGAAGGCAGCCACAATGGAGATCCCTATCCA T C ARFIP2 Ensembl:ENSG00000132254 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:6480301..6480476;chr11:6480301..6480734 26863196 MeRIP-seq:(Medium) rs201774105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870220,Human_RBP_ID_4184626,Human_RBP_ID_6084924,Human_RBP_ID_22895275,Human_RBP_ID_24913240 Human_Splice_Rec_1204522,Human_Splice_Rec_1204523,Human_Splice_Rec_1204536,Human_Splice_Rec_1204537,Human_Splice_Rec_1204550,Human_Splice_Rec_1204551,Human_Splice_Rec_1204564,Human_Splice_Rec_1204565,Human_Splice_Rec_1204600,Human_Splice_Rec_1204601,Human_Splice_Rec_1204612,Human_Splice_Rec_1204613,Human_Splice_Rec_1204616 Human_miRNA_ID_2047622 RMVar_hsa_circ_147830,RMVar_hsa_circ_90002 58141 RMVar_ID_58141 Human_SNP_ID_454698148 m1A Human chr11 - 6480934 6480934 6480934 GTGTATGAGACGGAGGAGGGGAGACCCCCTGAAGGAAGGGGGAAGAAACGCTAAAGGAATGTGAA GTGTATGAGACGGAGGAGGGGAGACCCCCTGACGGAAGGGGGAAGAAACGCTAAAGGAATGTGAA T G ARFIP2 Ensembl:ENSG00000132254 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:6480932..6481032 26863196 MeRIP-seq:(Medium) rs1270027969 Functional Loss SNV dbSNP153 33..33 33 - - - 58142 RMVar_ID_58142 Human_SNP_ID_454703547 m1A Human chr11 - 6502251 6502251 6502251 ATGCCTGTTACATTTTCTGCTCTTCCCCTACCATCACCCAACCTCTAGCTTCATATTCTTTCCTT ATGCCTGTTACATTTTCTGCTCTTCCCCTACCGTCACCCAACCTCTAGCTTCATATTCTTTCCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6502202..6502366 26863196 MeRIP-seq:(Medium) rs962438041 Functional Loss SNV dbSNP153 33..33 33 - - - 58143 RMVar_ID_58143 Human_SNP_ID_454719461 m1A Human chr11 + 6565765 6565765 6565765 ACGGACATGAAAGAGGAAGATGATGAGAGTGAAGAGAGTAATGAGGCTGAGGACCAGACAAAAGA ACGGACATGAAAGAGGAAGATGATGAGAGTGAGGAGAGTAATGAGGCTGAGGACCAGACAAAAGA A G DNHD1 Ensembl:ENSG00000179532 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:6565714..6565874 26863196 MeRIP-seq:(Medium) rs1449771696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5554431 Human_Splice_Rec_1204720,Human_Splice_Rec_1204828,Human_Splice_Rec_1204846,Human_Splice_Rec_1204862 RMVar_hsa_circ_122193,RMVar_hsa_circ_147865,RMVar_hsa_circ_99893,RMVar_hsa_circ_105014,RMVar_hsa_circ_147866,RMVar_hsa_circ_147864,RMVar_hsa_circ_105462,RMVar_hsa_circ_147867 58144 RMVar_ID_58144 Human_SNP_ID_454728863 m1A Human chr11 - 6601490 6601490 6601490 ACATTAAGCCGCAAGCAGTGGCGGAACCGGCAAAAGAACAAGAGAAGATGTAAGAACAAGTTTCA ACATTAAGCCGCAAGCAGTGGCGGAACCGGCAGAAGAACAAGAGAAGATGTAAGAACAAGTTTCA T C RRP8 Ensembl:ENSG00000132275 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6601444..6601594 26863196 MeRIP-seq:(Medium) rs1192993366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26319563 RMVar_hsa_circ_13756,RMVar_hsa_circ_112068,RMVar_hsa_circ_147868,RMVar_hsa_circ_346369,RMVar_hsa_circ_49083,RMVar_hsa_circ_42283 58145 RMVar_ID_58145 Human_SNP_ID_454729066 m1A Human chr11 - 6601901 6601901 6601901 GAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCCCCTATAAATTCAGCCCAGCACCTGGA GAAGATGAGAAAAGAAAGAGGAAATGCCAGAAGCATGCCCCTATAAATTCAGCCCAGCACCTGGA T C RRP8 Ensembl:ENSG00000132275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:6601843..6601935 26863196 MeRIP-seq:(Medium) rs982436514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940187,Human_RBP_ID_5344866,Human_RBP_ID_26319564,Human_RBP_ID_26804398,Human_RBP_ID_27803221 Human_Splice_Rec_1204913,Human_Splice_Rec_1204935,Human_Splice_Rec_1204943 RMVar_hsa_circ_13756,RMVar_hsa_circ_112068,RMVar_hsa_circ_147868,RMVar_hsa_circ_346369,RMVar_hsa_circ_42283 58146 RMVar_ID_58146 Human_SNP_ID_454729087 m1A Human chr11 + 6601969 6601969 6601969 AGAGTCACTGCCAACAAGAGCCTGTTTGTGGCATTTCTTCTTCCTTTCTACTTCTTCCTCAGAGT AGAGTCACTGCCAACAAGAGCCTGTTTGTGGCGTTTCTTCTTCCTTTCTACTTCTTCCTCAGAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6601918..6602074 26863196 MeRIP-seq:(Medium) rs369557794 Functional Loss SNV dbSNP153 33..33 33 - - - 58147 RMVar_ID_58147 Human_SNP_ID_454730030 m1A Human chr11 - 6604326 6604326 6604326 CTGGTTGAGGTCGTTCTCCGTGTTGTCCAGCCACAGGCGAACGGCGACTGCGTTGCCCTCCCGGC CTGGTTGAGGTCGTTCTCCGTGTTGTCCAGCCGCAGGCGAACGGCGACTGCGTTGCCCTCCCGGC T C AC091564.2 Ensembl:ENSG00000254400 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:6604224..6604393 26863196 MeRIP-seq:(Medium) rs767175625 Functional Loss SNV dbSNP153 33..33 33 - - - 58148 RMVar_ID_58148 Human_SNP_ID_454732034 m1A Human chr11 - 6610657 6610657 6610657 AGGCCTGCTGCTTTGGGGAGGTGCATTCCCCCAACCATGTCCCGACACCTCTGGAGTTCAGGCAA AGGCCTGCTGCTTTGGGGAGGTGCATTCCCCCGACCATGTCCCGACACCTCTGGAGTTCAGGCAA T C TAF10 Ensembl:ENSG00000166337 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:6610608..6610782 26863196 MeRIP-seq:(Medium) rs372079694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8356577 58149 RMVar_ID_58149 Human_SNP_ID_454732046 m1A Human chr11 - 6610699 6610699 6610699 GGCTGGGGTAGTACCATGACTGGAGGCGGGGGAGGCAACCAGAGGCCTGCTGCTTTGGGGAGGTG GGCTGGGGTAGTACCATGACTGGAGGCGGGGGGGGCAACCAGAGGCCTGCTGCTTTGGGGAGGTG T C TAF10 Ensembl:ENSG00000166337 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6610651..6610810 32194978 MeRIP-seq:(Medium) rs916910026 Functional Loss SNV dbSNP153 33..33 33 - - - 58150 RMVar_ID_58150 Human_SNP_ID_454732133 m1A Human chr11 - 6610950 6610950 6610950 CTTGACCCCTGCCCTCAGCGAGTATGGCATCAATGTGAAGAAGCCGCACTACTTCACCTGAGCCA CTTGACCCCTGCCCTCAGCGAGTATGGCATCACTGTGAAGAAGCCGCACTACTTCACCTGAGCCA T G AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6610926..6610950 26863196 MeRIP-seq:(Medium) rs202151101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401556,Human_RBP_ID_868617,Human_RBP_ID_1462326,Human_RBP_ID_1781671,Human_RBP_ID_4187152,Human_RBP_ID_5111281,Human_RBP_ID_5235183,Human_RBP_ID_17350472,Human_RBP_ID_17649481,Human_RBP_ID_18933299,Human_RBP_ID_21882828,Human_RBP_ID_23516194 Human_Splice_Rec_1205192,Human_Splice_Rec_1205196,Human_Splice_Rec_1205200,Human_Splice_Rec_1205228 Human_miRNA_ID_2022031,Human_miRNA_ID_2260574,Human_miRNA_ID_2263619,Human_miRNA_ID_2266688,Human_miRNA_ID_3151184,Human_miRNA_ID_3164954,Human_miRNA_ID_3165107,Human_miRNA_ID_3165260 RMVar_hsa_circ_81150,RMVar_hsa_circ_99612,RMVar_hsa_circ_147882,RMVar_hsa_circ_147883,RMVar_hsa_circ_147884 58151 RMVar_ID_58151 Human_SNP_ID_454732474 m1A Human chr11 - 6611777 6611777 6611777 CGGCGGGTGGCGCGGCGCCCCCGGAGGGGGCCATATCTAACGGGGTTTACGTACTGCCGAGCGCG CGGCGGGTGGCGCGGCGCCCCCGGAGGGGGCCGTATCTAACGGGGTTTACGTACTGCCGAGCGCG T C AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding exon,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:6611726..6612025 26863196 MeRIP-seq:(Medium) rs1334000944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401568,Human_RBP_ID_864794,Human_RBP_ID_988106,Human_RBP_ID_1462327,Human_RBP_ID_4185599,Human_RBP_ID_5093587,Human_RBP_ID_5644342,Human_RBP_ID_9321295,Human_RBP_ID_19049043 Human_Splice_Rec_1205186,Human_Splice_Rec_1205202,Human_Splice_Rec_1205208,Human_Splice_Rec_1205222 RMVar_hsa_circ_99612,RMVar_hsa_circ_147882 58152 RMVar_ID_58152 Human_SNP_ID_454732497 m1A Human chr11 + 6611802 6611802 6611802 TTAGATATGGCCCCCTCCGGGGGCGCCGCGCCACCCGCCGACACCGGAGCTGGAGGAGAACCAGC TTAGATATGGCCCCCTCCGGGGGCGCCGCGCCCCCCGCCGACACCGGAGCTGGAGGAGAACCAGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:6611751..6612200 26863196 MeRIP-seq:(Medium) rs776805315 Functional Loss SNV dbSNP153 33..33 33 - - - 58153 RMVar_ID_58153 Human_SNP_ID_454732609 m1A Human chr11 - 6612009 6612009 6612009 GGGGACCTGGGGCTGGAGCAGCTGCTGGGGGCACGGGACCCTTGGCGGCGCGGGCCGGGGAGCCA GGGGACCTGGGGCTGGAGCAGCTGCTGGGGGCGCGGGACCCTTGGCGGCGCGGGCCGGGGAGCCA T C AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:6611649..6612225;chr11:6611651..6612225 26863196 MeRIP-seq:(Medium) rs746816295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226111,Human_RBP_ID_401575,Human_RBP_ID_806796,Human_RBP_ID_1462329,Human_RBP_ID_4183940,Human_RBP_ID_5087114,Human_RBP_ID_5093541,Human_RBP_ID_5110350,Human_RBP_ID_5169861,Human_RBP_ID_5553623,Human_RBP_ID_5644343,Human_RBP_ID_8174135,Human_RBP_ID_9321296,Human_RBP_ID_19050958,Human_RBP_ID_27414932 Human_Splice_Rec_1205185,Human_Splice_Rec_1205207 RMVar_hsa_circ_99612,RMVar_hsa_circ_147882 58154 RMVar_ID_58154 Human_SNP_ID_454732618 m1A Human chr11 + 6612028 6612028 6612028 GCCAAGGGTCCCGTGCCCCCAGCAGCTGCTCCAGCCCCAGGTCCCCCCGCTGTCCCCGCGGGGCT GCCAAGGGTCCCGTGCCCCCAGCAGCTGCTCCGGCCCCAGGTCCCCCCGCTGTCCCCGCGGGGCT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:6611802..6612031 26863196 MeRIP-seq:(Medium) rs748001175 Functional Loss SNV dbSNP153 33..33 33 - - - 58155 RMVar_ID_58155 Human_SNP_ID_454732645 m1A Human chr11 + 6612103 6612103 6612103 TCCGCGGCGGTGCTGGAGGGCAGCGCGGCGGGAGCCGAGACCGGGGGCGCGGGGCCCGGGGCCGA TCCGCGGCGGTGCTGGAGGGCAGCGCGGCGGGGGCCGAGACCGGGGGCGCGGGGCCCGGGGCCGA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:6611751..6612169 26863410 MeRIP-seq:(Medium) rs1034532996 Functional Loss SNV dbSNP153 33..33 33 - - - 58156 RMVar_ID_58156 Human_SNP_ID_454732672 m1A Human chr11 - 6612158 6612158 6612158 GATGAGCTGCAGCGGCTCCGGCGCGGACCCCGAGGCGGCGCCGGCCTCCGCCGCCTCGGCCCCGG GATGAGCTGCAGCGGCTCCGGCGCGGACCCCGGGGCGGCGCCGGCCTCCGCCGCCTCGGCCCCGG T C AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding intron,CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:6611921..6612225 26863410 MeRIP-seq:(Medium) rs767768086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401579,Human_RBP_ID_806797,Human_RBP_ID_4183941,Human_RBP_ID_5169862,Human_RBP_ID_9321298 RMVar_hsa_circ_99612,RMVar_hsa_circ_147882 58157 RMVar_ID_58157 Human_SNP_ID_454745465 m1A Human chr11 - 6655754 6655754 6655754 GGCGGCTGTGCAGGAGGCGGCGCCCGGGCGTCAGCGGACGGACCGATCGACGGCCAAGGGCGCGC GGCGGCTGTGCAGGAGGCGGCGCCCGGGCGTCGGCGGACGGACCGATCGACGGCCAAGGGCGCGC T C DCHS1 Ensembl:ENSG00000166341 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:6655685..6655817 26863410 MeRIP-seq:(Medium) rs1474263709 Functional Loss SNV dbSNP153 33..33 33 - - - 58158 RMVar_ID_58158 Human_SNP_ID_454751869 m1A Human chr11 - 6682118 6682118 6682118 AGCTCCCACACAGCTCAAACACCAGGGATTTAACTGGATCTGAAGAGTCTGCAGCCCTTAATCAG AGCTCCCACACAGCTCAAACACCAGGGATTTAGCTGGATCTGAAGAGTCTGCAGCCCTTAATCAG T C MRPL17 Ensembl:ENSG00000158042 Protein coding stop codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:6682017..6682117 32194978 MeRIP-seq:(Medium) rs760354925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1459743,Human_RBP_ID_1781885,Human_RBP_ID_4175001,Human_RBP_ID_8357026,Human_RBP_ID_11686852,Human_RBP_ID_17649012,Human_RBP_ID_17800001,Human_RBP_ID_26895835 Human_miRNA_ID_2070535,Human_miRNA_ID_2803453 RMVar_hsa_circ_114617,RMVar_hsa_circ_147899 58159 RMVar_ID_58159 Human_SNP_ID_454752125 m1A Human chr11 + 6682814 6682814 6682814 CGTTAGTGTCTCCCAGCTTCCCATAGTCGATGAGCTGTGAGGACATAACATCACGGATCCAACCG CGTTAGTGTCTCCCAGCTTCCCATAGTCGATGGGCTGTGAGGACATAACATCACGGATCCAACCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:6682776..6682825;chr11:6682801..6682825 26863196 MeRIP-seq:(Medium) rs201914367 Functional Loss SNV dbSNP153 33..33 33 - - - 58160 RMVar_ID_58160 Human_SNP_ID_454752326 m1A Human chr11 + 6683279 6683279 6683279 CGGCGAAATACGCGGCCATGGGAGATCGCTGCAGCGACCGACAGCCGCATGTTTCCAACTTCTGC CGGCGAAATACGCGGCCATGGGAGATCGCTGCGGCGACCGACAGCCGCATGTTTCCAACTTCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:6683053..6683325;chr11:6683101..6683325 26863196 MeRIP-seq:(Medium) rs1484051756 Functional Loss SNV dbSNP153 33..33 33 - - - 58161 RMVar_ID_58161 Human_SNP_ID_454752345 m1A Human chr11 - 6683298 6683298 6683298 TCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAAACATGCGGCTGTCGGTCGCTGCAGCGATCTCCC TCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAAGCATGCGGCTGTCGGTCGCTGCAGCGATCTCCC T C MRPL17 Ensembl:ENSG00000158042 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:6683251..6683325 26863196 MeRIP-seq:(Medium) rs199806992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401894,Human_RBP_ID_751408,Human_RBP_ID_4175064,Human_RBP_ID_5460731,Human_RBP_ID_5490181,Human_RBP_ID_18416508 58162 RMVar_ID_58162 Human_SNP_ID_454752346 m1A Human chr11 - 6683298 6683298 6683298 TCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAAACATGCGGCTGTCGGTCGCTGCAGCGATCTCCC TCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAACCATGCGGCTGTCGGTCGCTGCAGCGATCTCCC T G MRPL17 Ensembl:ENSG00000158042 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:6683251..6683325 26863196 MeRIP-seq:(Medium) rs199806992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401894,Human_RBP_ID_751408,Human_RBP_ID_4175064,Human_RBP_ID_5460731,Human_RBP_ID_5490181,Human_RBP_ID_18416508 58163 RMVar_ID_58163 Human_SNP_ID_454752348 m1A Human chr11 - 6683300 6683300 6683300 GTTCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAAACATGCGGCTGTCGGTCGCTGCAGCGATCTC GTTCCGGCCTCCAAGGGGCGGGCAGAAGTTGGGAACATGCGGCTGTCGGTCGCTGCAGCGATCTC T C MRPL17 Ensembl:ENSG00000158042 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1286018082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401894,Human_RBP_ID_751408,Human_RBP_ID_4175064,Human_RBP_ID_5490181,Human_RBP_ID_18416508 58164 RMVar_ID_58164 Human_SNP_ID_454962811 m1A Human chr11 - 7514106 7514106 7514106 GGGGAGAGCCCACTGACCTGGGTACGGGGCCGAGGCTCCTCTCCGGGCGGCTCAGGTGTGCGGGC GGGGAGAGCCCACTGACCTGGGTACGGGGCCGCGGCTCCTCTCCGGGCGGCTCAGGTGTGCGGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:7514010..7514138 26863196 MeRIP-seq:(Medium) rs76560573 Functional Loss SNV dbSNP153 33..33 33 - - - 58165 RMVar_ID_58165 Human_SNP_ID_454964074 m1A Human chr11 + 7519067 7519067 7519067 AGGCAGTGCTAGAGTTGTCCTCAGGAGAGGACAGTGTAGGAAAAGAAGTGGGTACTGCTGACTGG AGGCAGTGCTAGAGTTGTCCTCAGGAGAGGACGGTGTAGGAAAAGAAGTGGGTACTGCTGACTGG A G PPFIBP2 Ensembl:ENSG00000166387 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:7518885..7519327 26863196 MeRIP-seq:(Medium) rs1000454831 Functional Loss SNV dbSNP153 33..33 33 - - - 58166 RMVar_ID_58166 Human_SNP_ID_455098636 m1A Human chr11 - 7987454 7987454 7987454 GAGGCTGGAGCCGCAGCGGGAACCGGAGCCGCAGCCGGTGCTGGCGTTGGCGCTGGAACTGAGGC GAGGCTGGAGCCGCAGCGGGAACCGGAGCCGCGGCCGGTGCTGGCGTTGGCGCTGGAACTGAGGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:7987351..7987576 26863196 MeRIP-seq:(Medium) rs1430191903 Functional Loss SNV dbSNP153 33..33 33 - - - 58167 RMVar_ID_58167 Human_SNP_ID_455098653 m1A Human chr11 + 7987481 7987481 7987481 CCGGCTGCGGCTCCGGTTCCCGCTGCGGCTCCAGCCTCATCCTCAGACCCTGCGGCAGCAGCGGC CCGGCTGCGGCTCCGGTTCCCGCTGCGGCTCCCGCCTCATCCTCAGACCCTGCGGCAGCAGCGGC A C EIF3F Ensembl:ENSG00000175390 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:7987326..7987650 26863410 MeRIP-seq:(Medium) rs753754616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404507,Human_RBP_ID_750523,Human_RBP_ID_9321949,Human_RBP_ID_17350028,Human_RBP_ID_17466930,Human_RBP_ID_18188165,Human_RBP_ID_22434206,Human_RBP_ID_26897960 Human_miRNA_ID_1024042,Human_miRNA_ID_1394226,Human_miRNA_ID_2466648,Human_miRNA_ID_2714620,Human_miRNA_ID_3050604 RMVar_hsa_circ_98732,RMVar_hsa_circ_115491,RMVar_hsa_circ_147919,RMVar_hsa_circ_147920,RMVar_hsa_circ_22566 58168 RMVar_ID_58168 Human_SNP_ID_455098658 m1A Human chr11 - 7987485 7987485 7987485 TGCAGCCGCTGCTGCCGCAGGGTCTGAGGATGAGGCTGGAGCCGCAGCGGGAACCGGAGCCGCAG TGCAGCCGCTGCTGCCGCAGGGTCTGAGGATGGGGCTGGAGCCGCAGCGGGAACCGGAGCCGCAG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:7987351..7987554 26863410 MeRIP-seq:(Medium) rs746100232 Functional Loss SNV dbSNP153 33..33 33 - - - 58169 RMVar_ID_58169 Human_SNP_ID_455098675 m1A Human chr11 - 7987514 7987514 7987514 GAGGCCGGGGTCTGGCCAGGAGCCGCAGTTGCAGCCGCTGCTGCCGCAGGGTCTGAGGATGAGGC GAGGCCGGGGTCTGGCCAGGAGCCGCAGTTGCGGCCGCTGCTGCCGCAGGGTCTGAGGATGAGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:7987376..7987550;chr11:7987351..7987550 32194978 MeRIP-seq:(Medium) rs372055041 Functional Loss SNV dbSNP153 33..33 33 - - - 58170 RMVar_ID_58170 Human_SNP_ID_455100813 m1A Human chr11 + 7994486 7994486 7994486 ATGGGAGTGATGTTCACGCCTCTGACAGTGAAATACGCGTACTACGACACTGAACGCATCGGAGG ATGGGAGTGATGTTCACGCCTCTGACAGTGAAGTACGCGTACTACGACACTGAACGCATCGGAGG A G EIF3F Ensembl:ENSG00000175390 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:7994426..7994525 32194978 MeRIP-seq:(Medium) rs1021979682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404514,Human_RBP_ID_808311,Human_RBP_ID_870968,Human_RBP_ID_1782984,Human_RBP_ID_5436955,Human_RBP_ID_5460882,Human_RBP_ID_5490429,Human_RBP_ID_17350029,Human_RBP_ID_22792330,Human_RBP_ID_23206820 Human_Splice_Rec_1206716,Human_Splice_Rec_1206717,Human_Splice_Rec_1206728,Human_Splice_Rec_1206729,Human_Splice_Rec_1206742,Human_Splice_Rec_1206743,Human_Splice_Rec_1206760,Human_Splice_Rec_1206761 RMVar_hsa_circ_10021,RMVar_hsa_circ_98732,RMVar_hsa_circ_115491,RMVar_hsa_circ_147919,RMVar_hsa_circ_147920,RMVar_hsa_circ_147921,RMVar_hsa_circ_84685,RMVar_hsa_circ_94194,RMVar_hsa_circ_147922,RMVar_hsa_circ_378323 58171 RMVar_ID_58171 Human_SNP_ID_455123352 m1A Human chr11 + 8081520 8081520 8081520 CCACCGCCCCGCCCCCGAGAGACATGACTTCCAAGCCGCATTCCGACTGGATTCCCTACAGGTAC CCACCGCCCCGCCCCCGAGAGACATGACTTCCGAGCCGCATTCCGACTGGATTCCCTACAGGTAC A G TUB Ensembl:ENSG00000166402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8081447..8081575 26863196 MeRIP-seq:(Medium) rs1159656048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17802057 Human_Splice_Rec_1206819 58172 RMVar_ID_58172 Human_SNP_ID_455164677 m1A Human chr11 + 8230411 8230411 8230411 ACTTGAGGCAGTCTTCGTGCCAGTACTTGTCCAATGCCTTCAGCAGATAGCGGTCCTTGATCTTG ACTTGAGGCAGTCTTCGTGCCAGTACTTGTCCGATGCCTTCAGCAGATAGCGGTCCTTGATCTTG A G HSALNG0082542 RNACentral:URS0000E9CCD3 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8230360..8230534 26863196 MeRIP-seq:(Medium) rs1170056796 Functional Loss SNV dbSNP153 33..33 33 - - - 58173 RMVar_ID_58173 Human_SNP_ID_455164693 m1A Human chr11 - 8230436 8230436 8230436 AGAAGGGCTGTGCGGGCTGTAACCGCAAGATCAAGGACCGCTATCTGCTGAAGGCATTGGACAAG AGAAGGGCTGTGCGGGCTGTAACCGCAAGATCGAGGACCGCTATCTGCTGAAGGCATTGGACAAG T C LMO1 Ensembl:ENSG00000166407 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8230343..8230536 26863196 MeRIP-seq:(Medium) rs767548965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1206942,Human_Splice_Rec_1206948,Human_Splice_Rec_1206954,Human_Splice_Rec_1206960 RMVar_hsa_circ_147936,RMVar_hsa_circ_267963,RMVar_hsa_circ_296573 58174 RMVar_ID_58174 Human_SNP_ID_455280484 m1A Human chr11 - 8682829 8682829 8682829 GGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAAACGAAACACCTACCATGTTGGCAGCCCAGACGA GGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAAGCGAAACACCTACCATGTTGGCAGCCCAGACGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8682806..8682958 26863196 MeRIP-seq:(Medium) rs780937350 Functional Loss SNV dbSNP153 33..33 33 - - - 58175 RMVar_ID_58175 Human_SNP_ID_455280485 m1A Human chr11 - 8682829 8682829 8682829 GGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAAACGAAACACCTACCATGTTGGCAGCCCAGACGA GGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAACCGAAACACCTACCATGTTGGCAGCCCAGACGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8682806..8682958 26863196 MeRIP-seq:(Medium) rs780937350 Functional Loss SNV dbSNP153 33..33 33 - - - 58176 RMVar_ID_58176 Human_SNP_ID_455280487 m1A Human chr11 - 8682833 8682833 8682833 TAGGGGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAAACGAAACACCTACCATGTTGGCAGCCCAG TAGGGGTCTCCGCCGGCAAGGAAGAGGAGGCAGGAAACGAAACACCTACCATGTTGGCAGCCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8682808..8682937 26863196 MeRIP-seq:(Medium) rs1260727399 Functional Loss SNV dbSNP153 33..33 33 - - - 58177 RMVar_ID_58177 Human_SNP_ID_455280488 m1A Human chr11 - 8682833 8682833 8682833 TAGGGGTCTCCGCCGGCAAGGAAGAGGAGGCAAGAAACGAAACACCTACCATGTTGGCAGCCCAG TAGGGGTCTCCGCCGGCAAGGAAGAGGAGGCACGAAACGAAACACCTACCATGTTGGCAGCCCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8682808..8682937 26863196 MeRIP-seq:(Medium) rs1260727399 Functional Loss SNV dbSNP153 33..33 33 - - - 58178 RMVar_ID_58178 Human_SNP_ID_455280694 m1A Human chr11 + 8683262 8683262 8683262 TTAGGGGCCACGTGAGCCACGGCCACGGCCGCATAGGTAAGTGCCGGCTTCCCCTCGGGGTGGGC TTAGGGGCCACGTGAGCCACGGCCACGGCCGCGTAGGTAAGTGCCGGCTTCCCCTCGGGGTGGGC A G RPL27A Ensembl:ENSG00000166441 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:8683201..8683275 32194978 MeRIP-seq:(Medium) rs748336698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227873,Human_RBP_ID_405517,Human_RBP_ID_988696,Human_RBP_ID_4184649,Human_RBP_ID_17648593,Human_RBP_ID_17802764,Human_RBP_ID_19050987,Human_RBP_ID_22434209 Human_Splice_Rec_1207418,Human_Splice_Rec_1207420,Human_Splice_Rec_1207421,Human_Splice_Rec_1207424,Human_Splice_Rec_1207425,Human_Splice_Rec_1207430,Human_Splice_Rec_1207431,Human_Splice_Rec_1207438,Human_Splice_Rec_1207439,Human_Splice_Rec_1207446,Human_Splice_Rec_1207447,Human_Splice_Rec_1207454,Human_Splice_Rec_1207455,Human_Splice_Rec_1207461,Human_Splice_Rec_1207467,Human_Splice_Rec_1207473 58179 RMVar_ID_58179 Human_SNP_ID_455280695 m1A Human chr11 - 8683263 8683263 8683263 GGCCCACCCCGAGGGGAAGCCGGCACTTACCTATGCGGCCGTGGCCGTGGCTCACGTGGCCCCTA GGCCCACCCCGAGGGGAAGCCGGCACTTACCTGTGCGGCCGTGGCCGTGGCTCACGTGGCCCCTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:8683201..8683275 32194978 MeRIP-seq:(Medium) rs1379720418 Functional Loss SNV dbSNP153 33..33 33 - - - 58180 RMVar_ID_58180 Human_SNP_ID_455280782 m1A Human chr11 - 8683491 8683491 8683491 GGTTCCACATCACAGCATTCCCACAGTACTCCATGTCTTCAACTAACCCAATACCGTGCCTGCTC GGTTCCACATCACAGCATTCCCACAGTACTCCGTGTCTTCAACTAACCCAATACCGTGCCTGCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8683475..8683654 26863196 MeRIP-seq:(Medium) rs143636617 Functional Loss SNV dbSNP153 33..33 33 - - - 58181 RMVar_ID_58181 Human_SNP_ID_455281319 m1A Human chr11 - 8684894 8684894 8684894 TATGGAAGTACAGAAAAACATCCAATTAACTTACCGATCGCACCACATCAATGATGGGAGCAGCC TATGGAAGTACAGAAAAACATCCAATTAACTTTCCGATCGCACCACATCAATGATGGGAGCAGCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr11:8684872..8684943;chr11:8684826..8684900 26863196,32194978 MeRIP-seq:(Medium) rs112715032 Functional Loss SNV dbSNP153 33..33 33 - - - 58182 RMVar_ID_58182 Human_SNP_ID_455281320 m1A Human chr11 - 8684894 8684894 8684894 TATGGAAGTACAGAAAAACATCCAATTAACTTACCGATCGCACCACATCAATGATGGGAGCAGCC TATGGAAGTACAGAAAAACATCCAATTAACTTCCCGATCGCACCACATCAATGATGGGAGCAGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr11:8684872..8684943;chr11:8684826..8684900 26863196,32194978 MeRIP-seq:(Medium) rs112715032 Functional Loss SNV dbSNP153 33..33 33 - - - 58183 RMVar_ID_58183 Human_SNP_ID_455281584 m1A Human chr11 + 8685628 8685628 8685628 GGGTTGGCAGTCTTTCCTCACGCCCATCACGCAGTTGGTACCTACTACAGTGTATTGTAAACTTT GGGTTGGCAGTCTTTCCTCACGCCCATCACGCCGTTGGTACCTACTACAGTGTATTGTAAACTTT A C RPL27A Ensembl:ENSG00000166441 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8685625..8685791 26863196 MeRIP-seq:(Medium) rs779089172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31211,Human_RBP_ID_2290576,Human_RBP_ID_11740991,Human_RBP_ID_22644062,Human_RBP_ID_24462572 RMVar_hsa_circ_91959,RMVar_hsa_circ_118057,RMVar_hsa_circ_147949,RMVar_hsa_circ_147950 58184 RMVar_ID_58184 Human_SNP_ID_455281585 m1A Human chr11 + 8685628 8685628 8685628 GGGTTGGCAGTCTTTCCTCACGCCCATCACGCAGTTGGTACCTACTACAGTGTATTGTAAACTTT GGGTTGGCAGTCTTTCCTCACGCCCATCACGCGGTTGGTACCTACTACAGTGTATTGTAAACTTT A G RPL27A Ensembl:ENSG00000166441 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8685625..8685791 26863196 MeRIP-seq:(Medium) rs779089172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31211,Human_RBP_ID_2290576,Human_RBP_ID_11740991,Human_RBP_ID_22644062,Human_RBP_ID_24462572 RMVar_hsa_circ_91959,RMVar_hsa_circ_118057,RMVar_hsa_circ_147949,RMVar_hsa_circ_147950 58185 RMVar_ID_58185 Human_SNP_ID_455281586 m1A Human chr11 + 8685628 8685628 8685628 GGGTTGGCAGTCTTTCCTCACGCCCATCACGCAGTTGGTACCTACTACAGTGTATTGTAAACTTT GGGTTGGCAGTCTTTCCTCACGCCCATCACGCTGTTGGTACCTACTACAGTGTATTGTAAACTTT A T RPL27A Ensembl:ENSG00000166441 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8685625..8685791 26863196 MeRIP-seq:(Medium) rs779089172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31211,Human_RBP_ID_2290576,Human_RBP_ID_11740991,Human_RBP_ID_22644062,Human_RBP_ID_24462572 RMVar_hsa_circ_91959,RMVar_hsa_circ_118057,RMVar_hsa_circ_147949,RMVar_hsa_circ_147950 58186 RMVar_ID_58186 Human_SNP_ID_455281614 m1A Human chr11 - 8685681 8685681 8685681 TGGGAGCTTTCCCTTTCCCAGAACTTTGTAGTAGCCCTAGAAGAACAGAGAAAAAAGTTTACAAT TGGGAGCTTTCCCTTTCCCAGAACTTTGTAGTGGCCCTAGAAGAACAGAGAAAAAAGTTTACAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:8685676..8685825 32194978 MeRIP-seq:(Medium) rs753975930 Functional Loss SNV dbSNP153 33..33 33 - - - 58187 RMVar_ID_58187 Human_SNP_ID_455282373 m1A Human chr11 + 8688049 8688037 8688050 ATTGGTCCAAGCAGAGGGAATACTGGTTCAGGAAACTGGTTTGGGAAGGTTAGGCAAACGGGAAG ATTGGTCCAAGCAGAGGGAAT_____________ACTGGTTTGGGAAGGTTAGGCAAACGGGAAG TACTGGTTCAGGAA T RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:8688001..8688210 26863196 MeRIP-seq:(Medium) rs1385068255 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_405585,Human_RBP_ID_6102733,Human_RBP_ID_11741117,Human_RBP_ID_17349617,Human_RBP_ID_18252984,Human_RBP_ID_23525685 RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 58188 RMVar_ID_58188 Human_SNP_ID_455286232 m1A Human chr11 - 8701511 8701511 8701511 GGAAGGAGAAAGGCAGAAAGAAGAAAGTACAGAGACAGAGGGAGAGAGGCTCCAAAGCCGAGAGA GGAAGGAGAAAGGCAGAAAGAAGAAAGTACAGCGACAGAGGGAGAGAGGCTCCAAAGCCGAGAGA T G DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8701461..8701600 26863196 MeRIP-seq:(Medium) rs57312436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23044,RMVar_hsa_circ_96914,RMVar_hsa_circ_125451,RMVar_hsa_circ_97643,RMVar_hsa_circ_89801,RMVar_hsa_circ_147953,RMVar_hsa_circ_147954,RMVar_hsa_circ_147955,RMVar_hsa_circ_147952,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_373913,RMVar_hsa_circ_147959 58189 RMVar_ID_58189 Human_SNP_ID_455286371 m1A Human chr11 + 8702024 8702024 8702024 ACCCACTCTCCTCTCTGCACCTCAGTGCCCCCATCACATCCTTCTCCCCAGCCCTCCCATTGCCC ACCCACTCTCCTCTCTGCACCTCAGTGCCCCCGTCACATCCTTCTCCCCAGCCCTCCCATTGCCC A G RPL27A Ensembl:ENSG00000166441 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:8701889..8702172 26863196 MeRIP-seq:(Medium) rs1203484083 Functional Loss SNV dbSNP153 33..33 33 - - - 58190 RMVar_ID_58190 Human_SNP_ID_455293670 m1A Human chr11 - 8730051 8730051 8730051 AAGAGTAAGCCCAGTAATGGTCTACCTCCTTCACCCACACCTGCTGCTCCACCTCCCTTGCCCTC AAGAGTAAGCCCAGTAATGGTCTACCTCCTTCGCCCACACCTGCTGCTCCACCTCCCTTGCCCTC T C DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8730000..8730194 26863196 MeRIP-seq:(Medium) rs759198980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27416807 Human_miRNA_ID_596260,Human_miRNA_ID_1237539,Human_miRNA_ID_1453310,Human_miRNA_ID_2100401,Human_miRNA_ID_2106349,Human_miRNA_ID_2112290,Human_miRNA_ID_2164843,Human_miRNA_ID_2221831,Human_miRNA_ID_2484887,Human_miRNA_ID_2596077,Human_miRNA_ID_2738998,Human_miRNA_ID_3039592,Human_miRNA_ID_3073263 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_81067,RMVar_hsa_circ_80502,RMVar_hsa_circ_147962,RMVar_hsa_circ_75978,RMVar_hsa_circ_147965,RMVar_hsa_circ_124340,RMVar_hsa_circ_147966,RMVar_hsa_circ_314841,RMVar_hsa_circ_147967,RMVar_hsa_circ_341464,RMVar_hsa_circ_14271,RMVar_hsa_circ_147968 58191 RMVar_ID_58191 Human_SNP_ID_455293687 m1A Human chr11 - 8730088 8730088 8730088 CAAGCGCACCTTTGAATACGAGGCTGACAAGAACCCCAAGAGTAAGCCCAGTAATGGTCTACCTC CAAGCGCACCTTTGAATACGAGGCTGACAAGAGCCCCAAGAGTAAGCCCAGTAATGGTCTACCTC T C DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:8729985..8730200 26863196 MeRIP-seq:(Medium) rs1292088855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2553985 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_81067,RMVar_hsa_circ_80502,RMVar_hsa_circ_147962,RMVar_hsa_circ_75978,RMVar_hsa_circ_147965,RMVar_hsa_circ_124340,RMVar_hsa_circ_147966,RMVar_hsa_circ_314841,RMVar_hsa_circ_147967,RMVar_hsa_circ_341464,RMVar_hsa_circ_14271,RMVar_hsa_circ_147968 58192 RMVar_ID_58192 Human_SNP_ID_455295740 m1A Human chr11 - 8737714 8737710 8737714 AGGAAGAGAAGAAAGAATGAAAGAAAGAAAAGAAAGGAGGGAGGGAGGAAGGAAGGAGAGAGAGA AGGAAGAGAAGAAAGAATGAAAGAAAGAAAAG____GAGGGAGGGAGGAAGGAAGGAGAGAGAGA CCTTT C DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8737709..8737882 26863196 MeRIP-seq:(Medium) rs1273040771 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_9651019 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_75978,RMVar_hsa_circ_147965,RMVar_hsa_circ_124340,RMVar_hsa_circ_147967,RMVar_hsa_circ_14271,RMVar_hsa_circ_147968 58193 RMVar_ID_58193 Human_SNP_ID_455310415 m1A Human chr11 + 8798011 8798011 8798011 ATCTGCACATTAACGGCTTCTTCTCATCCTTGAGCTCACAGTTCAAACGTCATTCTCAGAGGCCT ATCTGCACATTAACGGCTTCTTCTCATCCTTGGGCTCACAGTTCAAACGTCATTCTCAGAGGCCT A G AC026894.3 Ensembl:ENSG00000255159 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8798009..8798172 26863196 MeRIP-seq:(Medium) rs1423104866 Functional Loss SNV dbSNP153 33..33 33 - - - 58194 RMVar_ID_58194 Human_SNP_ID_455312825 m1A Human chr11 - 8806888 8806888 8806888 AAAAAAAAAAAAGACCATCTGGCATAGTCTGCAGAGATTTGTCTTTAAAGCCTATGGGAAAACTT AAAAAAAAAAAAGACCATCTGGCATAGTCTGCCGAGATTTGTCTTTAAAGCCTATGGGAAAACTT T G DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8806885..8807017 26863196 MeRIP-seq:(Medium) rs1338165833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_124340,RMVar_hsa_circ_147967,RMVar_hsa_circ_340433,RMVar_hsa_circ_291517,RMVar_hsa_circ_147969,RMVar_hsa_circ_147970 58195 RMVar_ID_58195 Human_SNP_ID_455313802 m1A Human chr11 - 8810614 8810614 8810614 GTCAGAGGAAGGAGCTGTGGGAAGCTCGCAGCAGGTATCGGAGCTTAAGCCAGTGGATTTGGGGG GTCAGAGGAAGGAGCTGTGGGAAGCTCGCAGCTGGTATCGGAGCTTAAGCCAGTGGATTTGGGGG T A DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8810464..8810636 26863196 MeRIP-seq:(Medium) rs914757215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1207561,Human_Splice_Rec_1207691,Human_Splice_Rec_1207857,Human_Splice_Rec_1207871,Human_Splice_Rec_1207895,Human_Splice_Rec_1207959,Human_Splice_Rec_1207967 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_124340,RMVar_hsa_circ_147967,RMVar_hsa_circ_340433,RMVar_hsa_circ_291517,RMVar_hsa_circ_147969,RMVar_hsa_circ_147970 58196 RMVar_ID_58196 Human_SNP_ID_455313803 m1A Human chr11 - 8810617 8810617 8810617 AAGGTCAGAGGAAGGAGCTGTGGGAAGCTCGCAGCAGGTATCGGAGCTTAAGCCAGTGGATTTGG AAGGTCAGAGGAAGGAGCTGTGGGAAGCTCGCTGCAGGTATCGGAGCTTAAGCCAGTGGATTTGG T A DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8810466..8810634 26863196 MeRIP-seq:(Medium) rs1194144177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1207959 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_124340,RMVar_hsa_circ_147967,RMVar_hsa_circ_340433,RMVar_hsa_circ_291517,RMVar_hsa_circ_147969,RMVar_hsa_circ_147970 58197 RMVar_ID_58197 Human_SNP_ID_455315037 m1A Human chr11 - 8815432 8815432 8815432 TTGGTAGCAGGGGAGGTGTGGGCAAGAGATGAAGCCAGAGGATTTCAGATTTGGGTGGGAGCGTA TTGGTAGCAGGGGAGGTGTGGGCAAGAGATGAGGCCAGAGGATTTCAGATTTGGGTGGGAGCGTA T C DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:8815427..8815532;chr11:8815428..8815614 26863196 MeRIP-seq:(Medium) rs1312816215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_124340,RMVar_hsa_circ_147967,RMVar_hsa_circ_147972,RMVar_hsa_circ_291517,RMVar_hsa_circ_147970,RMVar_hsa_circ_84238,RMVar_hsa_circ_302662,RMVar_hsa_circ_147973 58198 RMVar_ID_58198 Human_SNP_ID_455328571 m1A Human chr11 - 8871090 8871090 8871090 AAATCTGCGCTCCCTCCCCTCTCTCTCCCTGCAGCCCGGCCGCAGCCCGGGGCGCGGATGCCTGC AAATCTGCGCTCCCTCCCCTCTCTCTCCCTGCCGCCCGGCCGCAGCCCGGGGCGCGGATGCCTGC T G DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:8870913..8871206;chr11:8870711..8871358 26863196 MeRIP-seq:(Medium) rs1469178170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84238,RMVar_hsa_circ_147973 58199 RMVar_ID_58199 Human_SNP_ID_455328637 m1A Human chr11 + 8871271 8871271 8871271 GAGTGTGCGAGGGAGGGTGGGGGACAGGGGTGAGGGAGGCGGGGGCCGGGGGCAGCAGGGAGGAG GAGTGTGCGAGGGAGGGTGGGGGACAGGGGTGGGGGAGGCGGGGGCCGGGGGCAGCAGGGAGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8871265..8871352 26863196 MeRIP-seq:(Medium) rs1439733627 Functional Loss SNV dbSNP153 33..33 33 - - - 58200 RMVar_ID_58200 Human_SNP_ID_455338286 m1A Human chr11 - 8911225 8911225 8911225 TCTACCCCTTCCGCTACTTAGGGAGCCCCCTCACCCGGCTCACTCGTCAAGGCGCATGCGCGCAA TCTACCCCTTCCGCTACTTAGGGAGCCCCCTCGCCCGGCTCACTCGTCAAGGCGCATGCGCGCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:8911188..8911360;chr11:8911201..8911412;chr11:8911188..8911406 26863196 MeRIP-seq:(Medium) rs768073181 Functional Loss SNV dbSNP153 33..33 33 - - - 58201 RMVar_ID_58201 Human_SNP_ID_455338509 m1A Human chr11 + 8911668 8911668 8911668 CCGGCAGCCGGCCCGCAGCGCGTTCTCCCGGGAGAGGTGAGGGTCGCTGTGCCGGGGGCCGCCCC CCGGCAGCCGGCCCGCAGCGCGTTCTCCCGGGGGAGGTGAGGGTCGCTGTGCCGGGGGCCGCCCC A G AKIP1 Ensembl:ENSG00000166452 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8911426..8912520 26863196 MeRIP-seq:(Medium) rs780605091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19050998 Human_Splice_Rec_1208131,Human_Splice_Rec_1208139,Human_Splice_Rec_1208145,Human_Splice_Rec_1208151,Human_Splice_Rec_1208159,Human_Splice_Rec_1208167,Human_Splice_Rec_1208175,Human_Splice_Rec_1208180,Human_Splice_Rec_1208181,Human_Splice_Rec_1208189,Human_Splice_Rec_1208195,Human_Splice_Rec_1208203 RMVar_hsa_circ_46453 58202 RMVar_ID_58202 Human_SNP_ID_455338514 m1A Human chr11 - 8911673 8911673 8911673 GGACTGGGGCGGCCCCCGGCACAGCGACCCTCACCTCTCCCGGGAGAACGCGCTGCGGGCCGGCT GGACTGGGGCGGCCCCCGGCACAGCGACCCTCGCCTCTCCCGGGAGAACGCGCTGCGGGCCGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8911426..8911675 26863196 MeRIP-seq:(Medium) rs568250697 Functional Loss SNV dbSNP153 33..33 33 - - - 58203 RMVar_ID_58203 Human_SNP_ID_455339511 m1A Human chr11 + 8914902 8914902 8914902 CTATCGTTATCACAGAGGCGAGTCGAAGCTGCACATGTGCTTGGACATAGGGAATGGTCAGGTAA CTATCGTTATCACAGAGGCGAGTCGAAGCTGCGCATGTGCTTGGACATAGGGAATGGTCAGGTAA A G AKIP1 Ensembl:ENSG00000166452 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8914791..8917318 26863196 MeRIP-seq:(Medium) rs951974279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1208132,Human_Splice_Rec_1208133,Human_Splice_Rec_1208142,Human_Splice_Rec_1208143,Human_Splice_Rec_1208146,Human_Splice_Rec_1208147,Human_Splice_Rec_1208154,Human_Splice_Rec_1208155,Human_Splice_Rec_1208162,Human_Splice_Rec_1208163,Human_Splice_Rec_1208170,Human_Splice_Rec_1208171,Human_Splice_Rec_1208176,Human_Splice_Rec_1208177,Human_Splice_Rec_1208184,Human_Splice_Rec_1208185,Human_Splice_Rec_1208190,Human_Splice_Rec_1208191,Human_Splice_Rec_1208198,Human_Splice_Rec_1208199,Human_Splice_Rec_1208204,Human_Splice_Rec_1208205 Human_miRNA_ID_2012828,Human_miRNA_ID_2759208 RMVar_hsa_circ_40835,RMVar_hsa_circ_46453,RMVar_hsa_circ_330994,RMVar_hsa_circ_377868,RMVar_hsa_circ_147976,RMVar_hsa_circ_147977,RMVar_hsa_circ_147978 58204 RMVar_ID_58204 Human_SNP_ID_455340130 m1A Human chr11 + 8917235 8917235 8917235 TCCTAATAAGGTAGAAGAGAACTTCTCTTTACAATCCAAAAGTGAAAGCTTGGGCACAAATCAGT TCCTAATAAGGTAGAAGAGAACTTCTCTTTACCATCCAAAAGTGAAAGCTTGGGCACAAATCAGT A C AKIP1 Ensembl:ENSG00000166452 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:8917233..8917304 26863196 MeRIP-seq:(Medium) rs915038479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40835,RMVar_hsa_circ_377868,RMVar_hsa_circ_147977,RMVar_hsa_circ_147978 58205 RMVar_ID_58205 Human_SNP_ID_455350405 m1A Human chr11 - 8956250 8956250 8956250 GTGGAGCCCATGCCTGTGCGGGGGCCTGATGTAGAAGCATACTGTCTACGCTGTGAATGCAAATA GTGGAGCCCATGCCTGTGCGGGGGCCTGATGTGGAAGCATACTGTCTACGCTGTGAATGCAAATA T C TMEM9B Ensembl:ENSG00000175348 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:8953238..8962131 32194978 MeRIP-seq:(Medium) rs1166678115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4181454,Human_RBP_ID_22753363 Human_Splice_Rec_1208248,Human_Splice_Rec_1208249,Human_Splice_Rec_1208254,Human_Splice_Rec_1208255,Human_Splice_Rec_1208262,Human_Splice_Rec_1208263,Human_Splice_Rec_1208268,Human_Splice_Rec_1208269,Human_Splice_Rec_1208276,Human_Splice_Rec_1208277 58206 RMVar_ID_58206 Human_SNP_ID_455352386 m1A Human chr11 + 8964381 8964381 8964381 CCGCGACCGGCTCCCGGCTCGGGCTCAGGCTCAGGCTCAGGCTCAGGCACAGGCTTGGGACCCGG CCGCGACCGGCTCCCGGCTCGGGCTCAGGCTCGGGCTCAGGCTCAGGCACAGGCTTGGGACCCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8964274..8964382 26863196 MeRIP-seq:(Medium) rs1009700001 Functional Loss SNV dbSNP153 33..33 33 - - - 58207 RMVar_ID_58207 Human_SNP_ID_455354426 m1A Human chr11 + 8972206 8972206 8972206 TCAGATAATGAGATAGATTATGGAGGGGTTACAGTTTTTGGTAATAACGAGAGAGATCTAAGGTA TCAGATAATGAGATAGATTATGGAGGGGTTACGGTTTTTGGTAATAACGAGAGAGATCTAAGGTA A G TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:8972164..8972253 26863196 MeRIP-seq:(Medium) rs1192414185 Functional Loss SNV dbSNP153 33..33 33 - - - 58208 RMVar_ID_58208 Human_SNP_ID_455357047 m1A Human chr11 - 8980930 8980930 8980930 GTCTCATTCCTTATTAGATGTCTATCTCAAATAACAGAGTTTGAAAAATATTGGTTTTATCATTT GTCTCATTCCTTATTAGATGTCTATCTCAAATGACAGAGTTTGAAAAATATTGGTTTTATCATTT T C NRIP3 Ensembl:ENSG00000175352 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2568044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79930,RMVar_hsa_circ_112229,RMVar_hsa_circ_124010,RMVar_hsa_circ_122236,RMVar_hsa_circ_95094,RMVar_hsa_circ_147981,RMVar_hsa_circ_147983,RMVar_hsa_circ_147984,RMVar_hsa_circ_147985,RMVar_hsa_circ_147982 58209 RMVar_ID_58209 Human_SNP_ID_455405175 m1A Human chr11 - 9179014 9179014 9179014 AATAAGGATCTCAAAGTTCAGTGTGATGAAGAAGAACTCAGGATTTACCAGCTAAACATTCAGAT AATAAGGATCTCAAAGTTCAGTGTGATGAAGAGGAACTCAGGATTTACCAGCTAAACATTCAGAT T C DENND5A Ensembl:ENSG00000184014 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:9178963..9193566 32194978 MeRIP-seq:(Medium) rs1392869787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1783660,Human_RBP_ID_5520627,Human_RBP_ID_11745623,Human_RBP_ID_26318062,Human_RBP_ID_27803230 Human_Splice_Rec_1208580,Human_Splice_Rec_1208632,Human_Splice_Rec_1208744 RMVar_hsa_circ_106758,RMVar_hsa_circ_38541,RMVar_hsa_circ_372727,RMVar_hsa_circ_147995,RMVar_hsa_circ_148002,RMVar_hsa_circ_286023,RMVar_hsa_circ_81317,RMVar_hsa_circ_148006,RMVar_hsa_circ_22188,RMVar_hsa_circ_40751,RMVar_hsa_circ_335924,RMVar_hsa_circ_148021,RMVar_hsa_circ_287117,RMVar_hsa_circ_302214,RMVar_hsa_circ_288292,RMVar_hsa_circ_271236,RMVar_hsa_circ_148018,RMVar_hsa_circ_298540,RMVar_hsa_circ_266594,RMVar_hsa_circ_98585,RMVar_hsa_circ_148019,RMVar_hsa_circ_11709,RMVar_hsa_circ_347588,RMVar_hsa_circ_348338,RMVar_hsa_circ_303376,RMVar_hsa_circ_148023,RMVar_hsa_circ_148027,RMVar_hsa_circ_290774,RMVar_hsa_circ_313610,RMVar_hsa_circ_148020,RMVar_hsa_circ_316741,RMVar_hsa_circ_294296,RMVar_hsa_circ_275947,RMVar_hsa_circ_148025,RMVar_hsa_circ_148026,RMVar_hsa_circ_148024,RMVar_hsa_circ_50412 58210 RMVar_ID_58210 Human_SNP_ID_455411200 m1A Human chr11 + 9202686 9202680 9202687 TCTATACCATCTGGCCTCCAGTTAAGTCTCTAACACCATCTCCTACTATACTCCCGCTCATTCAC TCTATACCATCTGGCCTCCAGTTAAGT_______ACCATCTCCTACTATACTCCCGCTCATTCAC TCTCTAAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:9202684..9202991 26863196 MeRIP-seq:(Medium) rs1325678112 Functional Loss DEL dbSNP153 28..34 33 - - - 58211 RMVar_ID_58211 Human_SNP_ID_455411553 m1A Human chr11 - 9203963 9203963 9203963 AGTGCATCTGCCTCATCACACCCATGTCTTTCATGAAGGCATGTCGGAGCGTGCTGGAGCAACTC AGTGCATCTGCCTCATCACACCCATGTCTTTCGTGAAGGCATGTCGGAGCGTGCTGGAGCAACTC T C DENND5A Ensembl:ENSG00000184014 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:9203914..9206720 32194978 MeRIP-seq:(Medium) rs1470550721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4181792,Human_RBP_ID_9361973,Human_RBP_ID_17233417,Human_RBP_ID_17350031,Human_RBP_ID_18188171,Human_RBP_ID_26898786,Human_RBP_ID_27208209,Human_RBP_ID_27416885 Human_miRNA_ID_2195440,Human_miRNA_ID_2869877 RMVar_hsa_circ_4674,RMVar_hsa_circ_81317,RMVar_hsa_circ_148006,RMVar_hsa_circ_287117,RMVar_hsa_circ_302214,RMVar_hsa_circ_266594,RMVar_hsa_circ_347588,RMVar_hsa_circ_148027,RMVar_hsa_circ_290774,RMVar_hsa_circ_294296,RMVar_hsa_circ_148026,RMVar_hsa_circ_50412,RMVar_hsa_circ_35559,RMVar_hsa_circ_295900,RMVar_hsa_circ_299559,RMVar_hsa_circ_148028,RMVar_hsa_circ_276604,RMVar_hsa_circ_148030,RMVar_hsa_circ_148031,RMVar_hsa_circ_148029 58212 RMVar_ID_58212 Human_SNP_ID_455428555 m1A Human chr11 + 9265321 9265293 9265321 CCTCCGCGCCGCCGCCGCTGCAGCTAGCCGAGAGCGCCGCGGCCCGAGCGAGCCTGGAGAAGGGC CCTCC____________________________GCGCCGCGGCCCGAGCGAGCCTGGAGAAGGGC CGCGCCGCCGCCGCTGCAGCTAGCCGAGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:9265219..9265353 26863410 MeRIP-seq:(Medium) rs1313331276 Functional Loss DEL dbSNP153 6..33 33 - - - 58213 RMVar_ID_58213 Human_SNP_ID_455428562 m1A Human chr11 + 9265321 9265321 9265321 CCTCCGCGCCGCCGCCGCTGCAGCTAGCCGAGAGCGCCGCGGCCCGAGCGAGCCTGGAGAAGGGC CCTCCGCGCCGCCGCCGCTGCAGCTAGCCGAGGGCGCCGCGGCCCGAGCGAGCCTGGAGAAGGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:9265219..9265353 26863410 MeRIP-seq:(Medium) rs1193505761 Functional Loss SNV dbSNP153 33..33 33 - - - 58214 RMVar_ID_58214 Human_SNP_ID_455435445 m1A Human chr11 - 9289458 9289458 9289458 AAATGAGAACATGAGTAAAATGGGAACTAGAGAAAAAGGAATAGTTAATGAGTGAGGATAGATGG AAATGAGAACATGAGTAAAATGGGAACTAGAGGAAAAGGAATAGTTAATGAGTGAGGATAGATGG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:9289409..9289585 26863196 MeRIP-seq:(Medium) rs1020728650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21650,RMVar_hsa_circ_299863,RMVar_hsa_circ_284958,RMVar_hsa_circ_148038,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_288447,RMVar_hsa_circ_270143,RMVar_hsa_circ_148041,RMVar_hsa_circ_148043,RMVar_hsa_circ_282852,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 58215 RMVar_ID_58215 Human_SNP_ID_455457439 m1A Human chr11 - 9364141 9364140 9364141 GCACGGGAAAGTATTCCCCACCCCCCAGCGCAAGGAGGAAGTTAGCCTAAGACTAATTGAGGCAA GCACGGGAAAGTATTCCCCACCCCCCAGCGCA_GGAGGAAGTTAGCCTAAGACTAATTGAGGCAA CT C lnc-TMEM41B-10 RNACentral:URS0000D5C015 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:9364018..9364145 26863196 MeRIP-seq:(Medium) rs1346591851 Functional Loss DEL dbSNP153 33..33 33 - - - 58216 RMVar_ID_58216 Human_SNP_ID_455463616 m1A Human chr11 - 9384717 9384717 9384717 GGTCAAACCCGGGGCTCGGGTGCTACTGGGCCAGGAATAGCGCCACTCACTGCGCACATGGACCC GGTCAAACCCGGGGCTCGGGTGCTACTGGGCCGGGAATAGCGCCACTCACTGCGCACATGGACCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:9384670..9385068 26863196 MeRIP-seq:(Medium) rs981178827 Functional Loss SNV dbSNP153 33..33 33 - - - 58217 RMVar_ID_58217 Human_SNP_ID_455463675 m1A Human chr11 + 9384837 9384837 9384837 GGACCCAGCCCTGCGTGAGGCCGCGGAGCGCCAGCTCAATGAAGTAAGGACGCCCGGCTAGCGGT GGACCCAGCCCTGCGTGAGGCCGCGGAGCGCCGGCTCAATGAAGTAAGGACGCCCGGCTAGCGGT A G IPO7 Ensembl:ENSG00000205339 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:9384727..9384964 26863196 MeRIP-seq:(Medium) rs1273404507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406516,Human_RBP_ID_750812,Human_RBP_ID_871572,Human_RBP_ID_4184659,Human_RBP_ID_8773341,Human_RBP_ID_9275448,Human_RBP_ID_9321307,Human_RBP_ID_18188172,Human_RBP_ID_26803202 Human_Splice_Rec_1208861,Human_Splice_Rec_1208867,Human_Splice_Rec_1208913,Human_Splice_Rec_1208919 RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 58218 RMVar_ID_58218 Human_SNP_ID_455478953 m1A Human chr11 + 9438271 9438271 9438271 GAATGACAGTGATGATGATGATGAAGCTGAAGATGATGATGAAACCGGTAAGGGATTTTCAATGG GAATGACAGTGATGATGATGATGAAGCTGAAGCTGATGATGAAACCGGTAAGGGATTTTCAATGG A C IPO7 Ensembl:ENSG00000205339 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:9438226..9438300 26863196 MeRIP-seq:(Medium) rs772220602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17804939,Human_RBP_ID_23528008,Human_RBP_ID_26318066,Human_RBP_ID_27803234 Human_Splice_Rec_1208907 RMVar_hsa_circ_358273,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_127808,RMVar_hsa_circ_148061,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_318697,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_95475,RMVar_hsa_circ_31735,RMVar_hsa_circ_316929,RMVar_hsa_circ_148093,RMVar_hsa_circ_102630,RMVar_hsa_circ_367346,RMVar_hsa_circ_292076,RMVar_hsa_circ_326804,RMVar_hsa_circ_148094,RMVar_hsa_circ_24738,RMVar_hsa_circ_148096,RMVar_hsa_circ_148097,RMVar_hsa_circ_285855,RMVar_hsa_circ_314331,RMVar_hsa_circ_148098,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176 58219 RMVar_ID_58219 Human_SNP_ID_455478954 m1A Human chr11 + 9438271 9438271 9438271 GAATGACAGTGATGATGATGATGAAGCTGAAGATGATGATGAAACCGGTAAGGGATTTTCAATGG GAATGACAGTGATGATGATGATGAAGCTGAAGGTGATGATGAAACCGGTAAGGGATTTTCAATGG A G IPO7 Ensembl:ENSG00000205339 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:9438226..9438300 26863196 MeRIP-seq:(Medium) rs772220602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17804939,Human_RBP_ID_23528008,Human_RBP_ID_26318066,Human_RBP_ID_27803234 Human_Splice_Rec_1208907 RMVar_hsa_circ_358273,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_127808,RMVar_hsa_circ_148061,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_318697,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_95475,RMVar_hsa_circ_31735,RMVar_hsa_circ_316929,RMVar_hsa_circ_148093,RMVar_hsa_circ_102630,RMVar_hsa_circ_367346,RMVar_hsa_circ_292076,RMVar_hsa_circ_326804,RMVar_hsa_circ_148094,RMVar_hsa_circ_24738,RMVar_hsa_circ_148096,RMVar_hsa_circ_148097,RMVar_hsa_circ_285855,RMVar_hsa_circ_314331,RMVar_hsa_circ_148098,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176 58220 RMVar_ID_58220 Human_SNP_ID_455479615 m1A Human chr11 - 9440543 9440543 9440543 TCTTCAGCATCATCTTCTTCCCAATCTTCATCATCTCCATCTTCACCAGCCTGCTTAGCCAGAAT TCTTCAGCATCATCTTCTTCCCAATCTTCATCGTCTCCATCTTCACCAGCCTGCTTAGCCAGAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:9440476..9440575 26863196 MeRIP-seq:(Medium) rs373104388 Functional Loss SNV dbSNP153 33..33 33 - - - 58221 RMVar_ID_58221 Human_SNP_ID_455485475 m1A Human chr11 + 9461075 9461075 9461075 CGGACGAAGGAATTGTTGGAAAATTTTCTCGGAGGTTCGTATATAAATGTGTTTTTACCCAGTGT CGGACGAAGGAATTGTTGGAAAATTTTCTCGGGGGTTCGTATATAAATGTGTTTTTACCCAGTGT A G ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:9461033..9461108 26863196 MeRIP-seq:(Medium) rs1373627026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11755089 Human_Splice_Rec_1208971,Human_Splice_Rec_1209001,Human_Splice_Rec_1209011,Human_Splice_Rec_1209021,Human_Splice_Rec_1209049,Human_Splice_Rec_1209059,Human_Splice_Rec_1209071,Human_Splice_Rec_1209101,Human_Splice_Rec_1209111,Human_Splice_Rec_1209139,Human_Splice_Rec_1209149 58222 RMVar_ID_58222 Human_SNP_ID_455491158 m1A Human chr11 + 9478552 9478552 9478552 TCTGCACACTGGGGATGCTACAATTGACCCTGACACCATCAGTGCTTTGGAACAGTATGCAGCAA TCTGCACACTGGGGATGCTACAATTGACCCTGGCACCATCAGTGCTTTGGAACAGTATGCAGCAA A G ZNF143 Ensembl:ENSG00000166478 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:9478464..9478608 32194978 MeRIP-seq:(Medium) rs1373719028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18973324,Human_RBP_ID_27804249 Human_Splice_Rec_1208951,Human_Splice_Rec_1208981,Human_Splice_Rec_1209009,Human_Splice_Rec_1209029,Human_Splice_Rec_1209081,Human_Splice_Rec_1209119 RMVar_hsa_circ_34486,RMVar_hsa_circ_7369,RMVar_hsa_circ_316548,RMVar_hsa_circ_358630,RMVar_hsa_circ_73911,RMVar_hsa_circ_109232,RMVar_hsa_circ_367512,RMVar_hsa_circ_37825,RMVar_hsa_circ_38199,RMVar_hsa_circ_148106,RMVar_hsa_circ_265513,RMVar_hsa_circ_268350 58223 RMVar_ID_58223 Human_SNP_ID_455517224 m1A Human chr11 - 9573744 9573744 9573744 GGCTGCGGACGGTGGCGGCAGCGGCGGCGCGGACTTTCCGGCAGAGGCGGGGCGGCCCGAGCACC GGCTGCGGACGGTGGCGGCAGCGGCGGCGCGGCCTTTCCGGCAGAGGCGGGGCGGCCCGAGCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:9573651..9574351;chr11:9573676..9574275 26863196 MeRIP-seq:(Medium) rs1278103457 Functional Loss SNV dbSNP153 33..33 33 - - - 58224 RMVar_ID_58224 Human_SNP_ID_455517262 m1A Human chr11 + 9573847 9573847 9573847 CGCCGCGGCTGCGACTAGGCGCGCCCAGCCGCACGTGGCGGACCCGCCCCCAGGCCCGCAGTGTC CGCCGCGGCTGCGACTAGGCGCGCCCAGCCGCTCGTGGCGGACCCGCCCCCAGGCCCGCAGTGTC A T WEE1 Ensembl:ENSG00000166483 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:9573751..9573994 26863196 MeRIP-seq:(Medium) rs1281476089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184661,Human_RBP_ID_8774006,Human_RBP_ID_9275451,Human_RBP_ID_9363388 58225 RMVar_ID_58225 Human_SNP_ID_455517282 m1A Human chr11 - 9573901 9573901 9573901 CGCGGCCCTGGGGACGGGGCCGAGGACAGGAGAGCGGAGGCCTGCGGGGTCCAGGACACTGCGGG CGCGGCCCTGGGGACGGGGCCGAGGACAGGAGGGCGGAGGCCTGCGGGGTCCAGGACACTGCGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:9573676..9574300 26863196 MeRIP-seq:(Medium) rs1224125654 Functional Loss SNV dbSNP153 33..33 33 - - - 58226 RMVar_ID_58226 Human_SNP_ID_455539977 m1A Human chr11 - 9664142 9664142 9664142 CGGCCCTGCTGCCCCGCCAACCCCTCCTGCCCAGCCAGCCCCTCCGCGCCTCGGACGCCCCTCAA CGGCCCTGCTGCCCCGCCAACCCCTCCTGCCCTGCCAGCCCCTCCGCGCCTCGGACGCCCCTCAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:9664091..9664275 26863196 MeRIP-seq:(Medium) rs1349492436 Functional Loss SNV dbSNP153 33..33 33 - - - 58227 RMVar_ID_58227 Human_SNP_ID_455539978 m1A Human chr11 - 9664142 9664142 9664142 CGGCCCTGCTGCCCCGCCAACCCCTCCTGCCCAGCCAGCCCCTCCGCGCCTCGGACGCCCCTCAA CGGCCCTGCTGCCCCGCCAACCCCTCCTGCCCCGCCAGCCCCTCCGCGCCTCGGACGCCCCTCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:9664091..9664275 26863196 MeRIP-seq:(Medium) rs1349492436 Functional Loss SNV dbSNP153 33..33 33 - - - 58228 RMVar_ID_58228 Human_SNP_ID_455562115 m1A Human chr11 + 9748029 9748029 9748029 GCCATGGAGCAGCTGGAGCAGCTTGAGTTAGAACGGAAGCAAGCACTTGAGCAGTACGAGGTAAT GCCATGGAGCAGCTGGAGCAGCTTGAGTTAGAGCGGAAGCAAGCACTTGAGCAGTACGAGGTAAT A G SWAP70 Ensembl:ENSG00000133789 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:9747828..9748075 26863196 MeRIP-seq:(Medium) rs1227618854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5550448 Human_Splice_Rec_1209283,Human_Splice_Rec_1209305 RMVar_hsa_circ_26137,RMVar_hsa_circ_295435,RMVar_hsa_circ_22632,RMVar_hsa_circ_148120,RMVar_hsa_circ_352136,RMVar_hsa_circ_352981 58229 RMVar_ID_58229 Human_SNP_ID_455699687 m1A Human chr11 + 10282459 10282459 10282459 ACTTTTCTCCTTACCTCCTGACTCACATGTCTAAACACCTAAATGACATCTCTACCTTGATTATA ACTTTTCTCCTTACCTCCTGACTCACATGTCTGAACACCTAAATGACATCTCTACCTTGATTATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:10282456..10282547 26863196 MeRIP-seq:(Medium) rs755444216 Functional Loss SNV dbSNP153 33..33 33 - - - 58230 RMVar_ID_58230 Human_SNP_ID_455702778 m1A Human chr11 + 10294168 10294168 10294168 CCGGGAGGGCTCAGCATTTTCCCTGCAGCGGCAGTAGCGGCAGCGGCAGCGCTTCAGCCATGTTT CCGGGAGGGCTCAGCATTTTCCCTGCAGCGGCGGTAGCGGCAGCGGCAGCGCTTCAGCCATGTTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:10293714..10294176;chr11:10294024..10294187 26863196 MeRIP-seq:(Medium) rs1274026638 Functional Loss SNV dbSNP153 33..33 33 - - - 58231 RMVar_ID_58231 Human_SNP_ID_455702779 m1A Human chr11 - 10294170 10294170 10294170 TCAAACATGGCTGAAGCGCTGCCGCTGCCGCTACTGCCGCTGCAGGGAAAATGCTGAGCCCTCCC TCAAACATGGCTGAAGCGCTGCCGCTGCCGCTCCTGCCGCTGCAGGGAAAATGCTGAGCCCTCCC T G SBF2 Ensembl:ENSG00000133812 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:10294055..10294200 26863196 MeRIP-seq:(Medium) rs886047577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4145863,Human_RBP_ID_18416516 Clinvar_Rec_175 RMVar_hsa_circ_117770,RMVar_hsa_circ_95817,RMVar_hsa_circ_148177,RMVar_hsa_circ_148181 58232 RMVar_ID_58232 Human_SNP_ID_455756209 m1A Human chr11 - 10508163 10508163 10508163 TTTCAACCAGTGAAATTGACCTGCCCGTGAAGAGGCGGGCATAGTATAACAAGACGAGAAGACCC TTTCAACCAGTGAAATTGACCTGCCCGTGAAGGGGCGGGCATAGTATAACAAGACGAGAAGACCC T C MTRNR2L8 Ensembl:ENSG00000255823 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:10508101..10508297 26863410 MeRIP-seq:(Medium) rs1225390518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751821,Human_RBP_ID_22789503 58233 RMVar_ID_58233 Human_SNP_ID_455756256 m1A Human chr11 - 10508242 10508242 10508242 GTGCAAAGGTAGCATAATCACTTGTTCCTTAAATAGGGACTTGTATGAATGGCTCCACGAGGGTT GTGCAAAGGTAGCATAATCACTTGTTCCTTAAGTAGGGACTTGTATGAATGGCTCCACGAGGGTT T C MTRNR2L8 Ensembl:ENSG00000255823 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1443807828 Functional Loss SNV dbSNP153 33..33 33 - - - 58234 RMVar_ID_58234 Human_SNP_ID_455756257 m1A Human chr11 + 10508245 10508245 10508245 CCTCGTGGAGCCATTCATACAAGTCCCTATTTAAGGAACAAGTGATTATGCTACCTTTGCACAGT CCTCGTGGAGCCATTCATACAAGTCCCTATTTGAGGAACAAGTGATTATGCTACCTTTGCACAGT A G lnc-AMPD3-3 RNACentral:URS00008BDE77 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:10508128..10508343 26863196 MeRIP-seq:(Medium) rs1564862047 Functional Loss SNV dbSNP153 33..33 33 - - - 58235 RMVar_ID_58235 Human_SNP_ID_455756273 m1A Human chr11 + 10508275 10508275 10508275 TTAAGGAACAAGTGATTATGCTACCTTTGCACAGTTAGGGTACCGCGGCCGTTAAACGCATGTCA TTAAGGAACAAGTGATTATGCTACCTTTGCACGGTTAGGGTACCGCGGCCGTTAAACGCATGTCA A G lnc-AMPD3-3 RNACentral:URS00008BDE77 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr11:10508049..10508398;chr11:10508042..10508369 26863196 MeRIP-seq:(Medium) rs7350542 Functional Loss SNV dbSNP153 33..33 33 - - - 58236 RMVar_ID_58236 Human_SNP_ID_455756464 m1A Human chr11 - 10508826 10508826 10508826 CGAGTCTGGTGATAGCTGGTTGTCCAAGACAGAATCTTAGTTCAACTTTAAATTTACCCACAGAA CGAGTCTGGTGATAGCTGGTTGTCCAAGACAGGATCTTAGTTCAACTTTAAATTTACCCACAGAA T C MTRNR2L8 Ensembl:ENSG00000255823 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1035803614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17185253 58237 RMVar_ID_58237 Human_SNP_ID_455815163 m1A Human chr11 + 10751278 10751278 10751278 GTTGTTTAAGCGGCTGACGGGAAGGAGAAGCCAGAGCTCCAGCGGCGCCGCGGGGCGGCAGTCAA GTTGTTTAAGCGGCTGACGGGAAGGAGAAGCCGGAGCTCCAGCGGCGCCGCGGGGCGGCAGTCAA A G CTR9 Ensembl:ENSG00000198730 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:10751267..10751373 26863196 MeRIP-seq:(Medium) rs1304352173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752460,Human_RBP_ID_4184665 58238 RMVar_ID_58238 Human_SNP_ID_455815180 m1A Human chr11 + 10751315 10751315 10751315 TCCAGCGGCGCCGCGGGGCGGCAGTCAAGACCAGAGCCGGAGCCGTCACTCACCTCTGGATTAGC TCCAGCGGCGCCGCGGGGCGGCAGTCAAGACCTGAGCCGGAGCCGTCACTCACCTCTGGATTAGC A T CTR9 Ensembl:ENSG00000198730 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:10751265..10751370;chr11:10751265..10751376 26863196 MeRIP-seq:(Medium) rs1486474127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184665 58239 RMVar_ID_58239 Human_SNP_ID_455818251 m1A Human chr11 + 10764168 10764168 10764168 CAGTATCCCGATGATGTTGAAGCTTGGATTGAATTGGCACAAATCTTAGAACAGACTGATATACA CAGTATCCCGATGATGTTGAAGCTTGGATTGAGTTGGCACAAATCTTAGAACAGACTGATATACA A G CTR9 Ensembl:ENSG00000198730 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:10763784..10764180 26863196 MeRIP-seq:(Medium) rs957928118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31922,Human_RBP_ID_1774900,Human_RBP_ID_11511897 Human_Splice_Rec_1210430,Human_Splice_Rec_1210431 RMVar_hsa_circ_25857,RMVar_hsa_circ_117326,RMVar_hsa_circ_27958,RMVar_hsa_circ_42246,RMVar_hsa_circ_57912,RMVar_hsa_circ_107308,RMVar_hsa_circ_295794,RMVar_hsa_circ_148189,RMVar_hsa_circ_148190,RMVar_hsa_circ_148191 58240 RMVar_ID_58240 Human_SNP_ID_455820695 m1A Human chr11 - 10774104 10774104 10774104 TCCTCATCTTCACCTTCTTGTTCACTGCCACTACCCTTTCTTCTCTTCTTCTTTTTGGATATAGG TCCTCATCTTCACCTTCTTGTTCACTGCCACTGCCCTTTCTTCTCTTCTTCTTTTTGGATATAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:10774053..10774212 26863196 MeRIP-seq:(Medium) rs746166934 Functional Loss SNV dbSNP153 33..33 33 - - - 58241 RMVar_ID_58241 Human_SNP_ID_455820704 m1A Human chr11 + 10774136 10774136 10774136 TAGTGGCAGTGAACAAGAAGGTGAAGATGAGGAGGGTGGTGAGAGAAAGAAGAAAAAGAGGAGAA TAGTGGCAGTGAACAAGAAGGTGAAGATGAGGGGGGTGGTGAGAGAAAGAAGAAAAAGAGGAGAA A G CTR9 Ensembl:ENSG00000198730 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:10772555..10774213;chr11:10773960..10774231;chr11:10772572..10774230 26863196 MeRIP-seq:(Medium) rs1225288568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31930,Human_RBP_ID_193279,Human_RBP_ID_5166364,Human_RBP_ID_22034287,Human_RBP_ID_24542308,Human_RBP_ID_26318092,Human_RBP_ID_27803248 Human_Splice_Rec_1210455 Human_miRNA_ID_2171738 RMVar_hsa_circ_117326,RMVar_hsa_circ_107308,RMVar_hsa_circ_148189,RMVar_hsa_circ_65765,RMVar_hsa_circ_148191,RMVar_hsa_circ_54428,RMVar_hsa_circ_148192,RMVar_hsa_circ_101349,RMVar_hsa_circ_360634,RMVar_hsa_circ_361197 58242 RMVar_ID_58242 Human_SNP_ID_455829288 m1A Human chr11 - 10804369 10804369 10804369 AGAAGAGCCAAAGTATAGCTCACTGTATGCTCAGCTATGTCTGCGATTGGCAGAAGATGCACCAA AGAAGAGCCAAAGTATAGCTCACTGTATGCTCGGCTATGTCTGCGATTGGCAGAAGATGCACCAA T C EIF4G2 Ensembl:ENSG00000110321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:10804252..10804368 26863196 MeRIP-seq:(Medium) rs1161823956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_388390,Human_RBP_ID_985675,Human_RBP_ID_1453890,Human_RBP_ID_1775165,Human_RBP_ID_4187581,Human_RBP_ID_6041121,Human_RBP_ID_8344098,Human_RBP_ID_8766523,Human_RBP_ID_8997994,Human_RBP_ID_9274447,Human_RBP_ID_11516701,Human_RBP_ID_17789289,Human_RBP_ID_18602617,Human_RBP_ID_23485051,Human_RBP_ID_26803258,Human_RBP_ID_27197585,Human_RBP_ID_27614296 Human_Splice_Rec_1210504,Human_Splice_Rec_1210505,Human_Splice_Rec_1210544,Human_Splice_Rec_1210545,Human_Splice_Rec_1210579,Human_Splice_Rec_1210614,Human_Splice_Rec_1210615,Human_Splice_Rec_1210656,Human_Splice_Rec_1210657,Human_Splice_Rec_1210730,Human_Splice_Rec_1210731,Human_Splice_Rec_1210764,Human_Splice_Rec_1210765,Human_Splice_Rec_1210773,Human_Splice_Rec_1210790,Human_Splice_Rec_1210791,Human_Splice_Rec_1210797,Human_Splice_Rec_1210800,Human_Splice_Rec_1210801,Human_Splice_Rec_1210806,Human_Splice_Rec_1210814,Human_Splice_Rec_1210822,Human_Splice_Rec_1210830,Human_Splice_Rec_1210838,Human_Splice_Rec_1210850 RMVar_hsa_circ_108187,RMVar_hsa_circ_148195,RMVar_hsa_circ_84701,RMVar_hsa_circ_93069,RMVar_hsa_circ_148193,RMVar_hsa_circ_148194,RMVar_hsa_circ_13727,RMVar_hsa_circ_46090,RMVar_hsa_circ_301121,RMVar_hsa_circ_47004,RMVar_hsa_circ_346519,RMVar_hsa_circ_374422,RMVar_hsa_circ_148209,RMVar_hsa_circ_148210,RMVar_hsa_circ_370220,RMVar_hsa_circ_53958,RMVar_hsa_circ_103847,RMVar_hsa_circ_28479,RMVar_hsa_circ_125018,RMVar_hsa_circ_148215,RMVar_hsa_circ_148216,RMVar_hsa_circ_148217,RMVar_hsa_circ_307613,RMVar_hsa_circ_280734,RMVar_hsa_circ_22870,RMVar_hsa_circ_148218,RMVar_hsa_circ_148219,RMVar_hsa_circ_148221,RMVar_hsa_circ_366770,RMVar_hsa_circ_148222,RMVar_hsa_circ_327047 58243 RMVar_ID_58243 Human_SNP_ID_455829798 m1A Human chr11 + 10805999 10805999 10805999 GCGGAGTTGTCATCTCGTCTAGTGCTTCGTGCAGGAATCCATTTCTGAGCGTTTTGCCCTGGGGT GCGGAGTTGTCATCTCGTCTAGTGCTTCGTGCGGGAATCCATTTCTGAGCGTTTTGCCCTGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr11:10805950..10806048;chr11:10804922..10806013 26863196,32194978 MeRIP-seq:(Medium) rs753847685 Functional Loss SNV dbSNP153 33..33 33 - - - 58244 RMVar_ID_58244 Human_SNP_ID_455829800 m1A Human chr11 + 10806002 10806002 10806002 GAGTTGTCATCTCGTCTAGTGCTTCGTGCAGGAATCCATTTCTGAGCGTTTTGCCCTGGGGTTTT GAGTTGTCATCTCGTCTAGTGCTTCGTGCAGGGATCCATTTCTGAGCGTTTTGCCCTGGGGTTTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:10805951..10806050 32194978 MeRIP-seq:(Medium) rs757718007 Functional Loss SNV dbSNP153 33..33 33 - - - 58245 RMVar_ID_58245 Human_SNP_ID_455830285 m1A Human chr11 + 10807354 10807349 10807354 TCAAAAGAATAATATTAATAGATGGGGTGGGGAGGGGAGGGGACAGGAGAAATGAAATACCTGGA TCAAAAGAATAATATTAATAGATGGGGT_____GGGGAGGGGACAGGAGAAATGAAATACCTGGA TGGGGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:10807255..10807405;chr11:10807276..10807400 32194978 MeRIP-seq:(Medium) rs748410370 Functional Loss DEL dbSNP153 29..33 33 - - - 58246 RMVar_ID_58246 Human_SNP_ID_455830288 m1A Human chr11 + 10807354 10807354 10807354 TCAAAAGAATAATATTAATAGATGGGGTGGGGAGGGGAGGGGACAGGAGAAATGAAATACCTGGA TCAAAAGAATAATATTAATAGATGGGGTGGGGGGGGGAGGGGACAGGAGAAATGAAATACCTGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:10807255..10807405;chr11:10807276..10807400 32194978 MeRIP-seq:(Medium) rs747849622 Functional Loss SNV dbSNP153 33..33 33 - - - 58247 RMVar_ID_58247 Human_SNP_ID_455830302 m1A Human chr11 - 10807383 10807383 10807383 CAGTGTCTAATTTTGGTGCTCTTTCTCGTTCCAGGTATTTCATTTCTCCTGTCCCCTCCCCTCCC CAGTGTCTAATTTTGGTGCTCTTTCTCGTTCCGGGTATTTCATTTCTCCTGTCCCCTCCCCTCCC T C EIF4G2 Ensembl:ENSG00000110321 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:10807351..10807400 26863196 MeRIP-seq:(Medium) rs1298794921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22568676,Human_RBP_ID_22644075,Human_RBP_ID_22735979,Human_RBP_ID_24458680,Human_RBP_ID_24866794 Human_Splice_Rec_1210809,Human_Splice_Rec_1210817 RMVar_hsa_circ_84701,RMVar_hsa_circ_148193 58248 RMVar_ID_58248 Human_SNP_ID_455830689 m1A Human chr11 - 10808428 10808365 10808428 GGCCGACGCCTGCAGGGACGAGGCCGTGGCGGACCGAGGCACGGCTGTGCTCGGACGGCGAGGGA GGCCGACGCCTGCAGGGACGAGGCCGTGGCGG_________________________________ CCCGCCACGGCGCTAGCGGTCCGAGCCACGCTCCCTCGCCGTCCGAGCACAGCCGTGCCTCGGT C EIF4G2 Ensembl:ENSG00000110321 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:10808426..10808525 26863196 MeRIP-seq:(Medium) rs1564986535 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5343432,Human_RBP_ID_6041175,Human_RBP_ID_11516884,Human_RBP_ID_17109034,Human_RBP_ID_18477620 Human_Splice_Rec_1210780 RMVar_hsa_circ_84701,RMVar_hsa_circ_148193 58249 RMVar_ID_58249 Human_SNP_ID_455830930 m1A Human chr11 - 10808867 10808864 10808867 GGTGGCAGCGGGTACCGAGTGGCGGCTGCAGCAGCGACTCCTCTGAGCTGAGTTTGAGGCCGTCC GGTGGCAGCGGGTACCGAGTGGCGGCTGCAGC___GACTCCTCTGAGCTGAGTTTGAGGCCGTCC CGCT C EIF4G2 Ensembl:ENSG00000110321 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:10808776..10808900 26863410 MeRIP-seq:(Medium) rs1200085438 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_226387,Human_RBP_ID_388411,Human_RBP_ID_4146910,Human_RBP_ID_5313566,Human_RBP_ID_5461109,Human_RBP_ID_6041183,Human_RBP_ID_11516903,Human_RBP_ID_22434223,Human_RBP_ID_23124069,Human_RBP_ID_23485090 RMVar_hsa_circ_84701,RMVar_hsa_circ_148193 58250 RMVar_ID_58250 Human_SNP_ID_455830937 m1A Human chr11 + 10808880 10808880 10808880 CTCAGCTCAGAGGAGTCGCTGCTGCAGCCGCCACTCGGTACCCGCTGCCACCTCCATAGAGCTCC CTCAGCTCAGAGGAGTCGCTGCTGCAGCCGCCGCTCGGTACCCGCTGCCACCTCCATAGAGCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:10808070..10808950;chr11:10808099..10808950;chr11:10808701..10808950 26863196 MeRIP-seq:(Medium) rs999148150 Functional Loss SNV dbSNP153 33..33 33 - - - 58251 RMVar_ID_58251 Human_SNP_ID_455842892 m1A Human chr11 + 10857928 10857928 10857928 CGTCGTGGACTGGAGGGGGAGGGGAGAGAGGGAGGGGAATGAAAAACAAAACAGAGAGGAAAGAA CGTCGTGGACTGGAGGGGGAGGGGAGAGAGGGGGGGGAATGAAAAACAAAACAGAGAGGAAAGAA A G ZBED5-AS1,LOC101928053,ZBED5-AS1:2,ZBED5-AS1:3 RNACentral:URS00008B372D,RNACentral:URS00008BB4E1,RNACentral:URS0000D5717D,RNACentral:URS00008BC366 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:10857877..10858032 26863196 MeRIP-seq:(Medium) rs983513791 Functional Loss SNV dbSNP153 33..33 33 - - - 58252 RMVar_ID_58252 Human_SNP_ID_455842915 m1A Human chr11 - 10858004 10858004 10858004 AGCCGCGAATCGGATCTCTATGGAGATGGCCTAGGCGATATCCCTGAGCTGAGAGCATCACCCTG AGCCGCGAATCGGATCTCTATGGAGATGGCCTGGGCGATATCCCTGAGCTGAGAGCATCACCCTG T C ZBED5 Ensembl:ENSG00000236287 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:10857555..10858021;chr11:10857856..10858016 26863196 MeRIP-seq:(Medium) rs974467231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184667,Human_RBP_ID_11519277,Human_RBP_ID_17789442,Human_RBP_ID_18416517 58253 RMVar_ID_58253 Human_SNP_ID_455860297 m1A Human chr11 + 10931415 10931415 10931415 GGTGAGCGGCCGTAATGAGCACTCGCAGGAGCAAGGGGCCCGGCGCGGGCCTCCAGGGCGGGAGG GGTGAGCGGCCGTAATGAGCACTCGCAGGAGCGAGGGGCCCGGCGCGGGCCTCCAGGGCGGGAGG A G lnc-CTR9-5,lnc-CTR9-5:2,lnc-CTR9-5:3,lnc-CTR9-5:4,lnc-CTR9-5:5 RNACentral:URS00008BD1AA,RNACentral:URS0000D5E3B0,RNACentral:URS0000D58D4C,RNACentral:URS00009C46FE,RNACentral:URS00008BD5BA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:10931062..10931660 26863196 MeRIP-seq:(Medium) rs1457226324 Functional Loss SNV dbSNP153 33..33 33 - - - 58254 RMVar_ID_58254 Human_SNP_ID_455860341 m1A Human chr11 + 10931531 10931531 10931531 GTGCGGAGGCCGGGACGGAGCAGCGCGTAACTAGGGAGAGGATAGGCCGGGCTGGTGGAGATGCG GTGCGGAGGCCGGGACGGAGCAGCGCGTAACTGGGGAGAGGATAGGCCGGGCTGGTGGAGATGCG A G lnc-CTR9-5,lnc-CTR9-5:2,lnc-CTR9-5:3,lnc-CTR9-5:4,lnc-CTR9-5:5 RNACentral:URS00008BD1AA,RNACentral:URS0000D5E3B0,RNACentral:URS0000D58D4C,RNACentral:URS00009C46FE,RNACentral:URS00008BD5BA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:10931375..10931627 26863196 MeRIP-seq:(Medium) rs920417234 Functional Loss SNV dbSNP153 33..33 33 - - - 58255 RMVar_ID_58255 Human_SNP_ID_455860347 m1A Human chr11 - 10931541 10931541 10931541 GGTCTCTCCCCGCATCTCCACCAGCCCGGCCTATCCTCTCCCTAGTTACGCGCTGCTCCGTCCCG GGTCTCTCCCCGCATCTCCACCAGCCCGGCCTGTCCTCTCCCTAGTTACGCGCTGCTCCGTCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:10931201..10931669 26863196 MeRIP-seq:(Medium) rs796164054 Functional Loss SNV dbSNP153 33..33 33 - - - 58256 RMVar_ID_58256 Human_SNP_ID_455860585 m1A Human chr11 - 10932267 10932267 10932267 CCTCTGCTCTCTTCCTCCTCTCCTTGACCCCCACTGCTTCCTCCTCCTCCTCTCTCCTTCCTCCA CCTCTGCTCTCTTCCTCCTCTCCTTGACCCCCCCTGCTTCCTCCTCCTCCTCTCTCCTTCCTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:10932224..10932415 26863196 MeRIP-seq:(Medium) rs1415358368 Functional Loss SNV dbSNP153 33..33 33 - - - 58257 RMVar_ID_58257 Human_SNP_ID_456090156 m1A Human chr11 + 11842242 11842242 11842242 CTGGTCCCGAAAGAGGTGAGGGGCCCCAGAGGAGGTTAGGCCTTAGGCCTGCGGCCGCTCGAGGC CTGGTCCCGAAAGAGGTGAGGGGCCCCAGAGGTGGTTAGGCCTTAGGCCTGCGGCCGCTCGAGGC A T USP47 Ensembl:ENSG00000170242 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:11842236..11842347 26863196 MeRIP-seq:(Medium) rs1262769112 Functional Loss SNV dbSNP153 33..33 33 - - - 58258 RMVar_ID_58258 Human_SNP_ID_456106841 m1A Human chr11 + 11912179 11912179 11912179 GCTTCCACCTAACCTGAAAAAAGAAGAGCAAAAGAAACCCAAAGCAAGCGGAAGGAAGGACATAA GCTTCCACCTAACCTGAAAAAAGAAGAGCAAAGGAAACCCAAAGCAAGCGGAAGGAAGGACATAA A G USP47 Ensembl:ENSG00000170242 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:11912120..11912212 26863196 MeRIP-seq:(Medium) rs533245943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319460,RMVar_hsa_circ_1337,RMVar_hsa_circ_148248,RMVar_hsa_circ_31179,RMVar_hsa_circ_322492,RMVar_hsa_circ_341654,RMVar_hsa_circ_353541,RMVar_hsa_circ_371745,RMVar_hsa_circ_148245,RMVar_hsa_circ_148246,RMVar_hsa_circ_325356,RMVar_hsa_circ_352489,RMVar_hsa_circ_107331,RMVar_hsa_circ_43676,RMVar_hsa_circ_61156,RMVar_hsa_circ_342505,RMVar_hsa_circ_350517,RMVar_hsa_circ_328945,RMVar_hsa_circ_34005,RMVar_hsa_circ_34448,RMVar_hsa_circ_6154,RMVar_hsa_circ_148249,RMVar_hsa_circ_148250 58259 RMVar_ID_58259 Human_SNP_ID_456117836 m1A Human chr11 + 11958127 11958127 11958127 GGGTTTCTGCTTTAAAGGACTGACTTGCTATCACACAAAAGAGGCAGACTTGTAAACACAATGGG GGGTTTCTGCTTTAAAGGACTGACTTGCTATCGCACAAAAGAGGCAGACTTGTAAACACAATGGG A G USP47 Ensembl:ENSG00000170242 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1979687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_321465,Human_miRNA_ID_1008572 GWAS_ID_6822,GWAS_ID_6823,GWAS_ID_6824,GWAS_ID_6825 58260 RMVar_ID_58260 Human_SNP_ID_456119024 m1A Human chr11 + 11963304 11963304 11963304 GGAGTGGCGTAGAGTTCAGTGTTCGCAGTCGCATATTACAACCATGTTTCACACAGCCCTGCTCG GGAGTGGCGTAGAGTTCAGTGTTCGCAGTCGCTTATTACAACCATGTTTCACACAGCCCTGCTCG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:11963254..11963354 32194978 MeRIP-seq:(Medium) rs942760847 Functional Loss SNV dbSNP153 33..33 33 - - - 58261 RMVar_ID_58261 Human_SNP_ID_456119199 m1A Human chr11 + 11964098 11964097 11964098 GCAAAGCAGGGCACTCTTCTCCACATTTCCCCAAAACCAATCAGAGGGAGACTCCACATTGTTTC GCAAAGCAGGGCACTCTTCTCCACATTTCCCC_AAACCAATCAGAGGGAGACTCCACATTGTTTC CA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:11964047..11964197 32194978 MeRIP-seq:(Medium) rs1314010568 Functional Loss DEL dbSNP153 33..33 33 - - - 58262 RMVar_ID_58262 Human_SNP_ID_456119300 m1A Human chr11 + 11964491 11964491 11964491 CAGATCTAAATCTCTTCCCCTCCCAGCAGTGCAGCGGCGGCAGCCGCAGGCTCCCTCAGCGCCAT CAGATCTAAATCTCTTCCCCTCCCAGCAGTGCGGCGGCGGCAGCCGCAGGCTCCCTCAGCGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:11964440..11964637 26863196 MeRIP-seq:(Medium) rs781567445 Functional Loss SNV dbSNP153 33..33 33 - - - 58263 RMVar_ID_58263 Human_SNP_ID_456119332 m1A Human chr11 - 11964527 11964527 11964527 GAGCTGGAGGACCTGGAGAGGAGCCTGACTGAAGAGATGGCGCTGAGGGAGCCTGCGGCTGCCGC GAGCTGGAGGACCTGGAGAGGAGCCTGACTGAGGAGATGGCGCTGAGGGAGCCTGCGGCTGCCGC T C DKK3 Ensembl:ENSG00000050165 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:11964477..11964603 26863196 MeRIP-seq:(Medium) rs1442141496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148256,RMVar_hsa_circ_97794 58264 RMVar_ID_58264 Human_SNP_ID_456130283 m1A Human chr11 - 12008610 12008610 12008610 CCGCGCGCCTCTGATCGCGTTCCGGGACACACAGGCGGCGGCTGCGGGCGCAGAGCGGAGATGCA CCGCGCGCCTCTGATCGCGTTCCGGGACACACTGGCGGCGGCTGCGGGCGCAGAGCGGAGATGCA T A DKK3 Ensembl:ENSG00000050165 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:12008568..12008907 32194978 MeRIP-seq:(Medium) rs1004396369 Functional Loss SNV dbSNP153 33..33 33 - - - 58265 RMVar_ID_58265 Human_SNP_ID_456130284 m1A Human chr11 - 12008610 12008610 12008610 CCGCGCGCCTCTGATCGCGTTCCGGGACACACAGGCGGCGGCTGCGGGCGCAGAGCGGAGATGCA CCGCGCGCCTCTGATCGCGTTCCGGGACACACGGGCGGCGGCTGCGGGCGCAGAGCGGAGATGCA T C DKK3 Ensembl:ENSG00000050165 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:12008568..12008907 32194978 MeRIP-seq:(Medium) rs1004396369 Functional Loss SNV dbSNP153 33..33 33 - - - 58266 RMVar_ID_58266 Human_SNP_ID_456173509 m1A Human chr11 + 12175761 12175761 12175761 TAAAGGAGCAAGGTGATGAGTGTGCAGTTCTTAGAGGGGAGTGAATGCTAGGCAAAGGAGCAGCA TAAAGGAGCAAGGTGATGAGTGTGCAGTTCTTGGAGGGGAGTGAATGCTAGGCAAAGGAGCAGCA A G MICAL2 Ensembl:ENSG00000133816 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12175752..12175851 26863196 MeRIP-seq:(Medium) rs1313216558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15749,RMVar_hsa_circ_114181,RMVar_hsa_circ_79804,RMVar_hsa_circ_148263,RMVar_hsa_circ_11060,RMVar_hsa_circ_148262 58267 RMVar_ID_58267 Human_SNP_ID_456225640 m1A Human chr11 + 12377620 12377593 12377620 CTGCGTCCGCCCAGCGCCAGCTCCGCGTCCCGACCGGCCCGCGGCAGCCTGCGCCGCGCCATGGC CTGCGT___________________________CCGGCCCGCGGCAGCCTGCGCCGCGCCATGGC TCCGCCCAGCGCCAGCTCCGCGTCCCGA T PARVA Ensembl:ENSG00000197702 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12377576..12377859 26863196 MeRIP-seq:(Medium) rs746644973 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_4185633 58268 RMVar_ID_58268 Human_SNP_ID_456225670 m1A Human chr11 + 12377633 12377633 12377633 GCGCCAGCTCCGCGTCCCGACCGGCCCGCGGCAGCCTGCGCCGCGCCATGGCCACCTCCCCGCAG GCGCCAGCTCCGCGTCCCGACCGGCCCGCGGCTGCCTGCGCCGCGCCATGGCCACCTCCCCGCAG A T PARVA Ensembl:ENSG00000197702 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:12377576..12377725 26863410 MeRIP-seq:(Medium) rs1451729338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185633 58269 RMVar_ID_58269 Human_SNP_ID_456251121 m1A Human chr11 + 12485247 12485247 12485247 GCCTCTGTTAATTTTGGTGCTAATGGAGGGAAAATGCTGTAGAGTCCAGGAGCCAGTGGGTAGAT GCCTCTGTTAATTTTGGTGCTAATGGAGGGAACATGCTGTAGAGTCCAGGAGCCAGTGGGTAGAT A C PARVA Ensembl:ENSG00000197702 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12485214..12485356 26863196 MeRIP-seq:(Medium) rs898185938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27374,RMVar_hsa_circ_48335,RMVar_hsa_circ_367395 58270 RMVar_ID_58270 Human_SNP_ID_456251122 m1A Human chr11 + 12485247 12485247 12485247 GCCTCTGTTAATTTTGGTGCTAATGGAGGGAAAATGCTGTAGAGTCCAGGAGCCAGTGGGTAGAT GCCTCTGTTAATTTTGGTGCTAATGGAGGGAATATGCTGTAGAGTCCAGGAGCCAGTGGGTAGAT A T PARVA Ensembl:ENSG00000197702 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12485214..12485356 26863196 MeRIP-seq:(Medium) rs898185938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27374,RMVar_hsa_circ_48335,RMVar_hsa_circ_367395 58271 RMVar_ID_58271 Human_SNP_ID_456263359 m1A Human chr11 + 12533856 12533856 12533856 GGAGGAGGAGTAGGGGTTGGTCTTGCTGTCTGAGGGGTGGCAGAGGCAGAAAAAAAATCCATGGG GGAGGAGGAGTAGGGGTTGGTCTTGCTGTCTGGGGGGTGGCAGAGGCAGAAAAAAAATCCATGGG A G PARVA Ensembl:ENSG00000197702 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:12533805..12533887 26863196 MeRIP-seq:(Medium) rs1253496214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148278,RMVar_hsa_circ_102185 58272 RMVar_ID_58272 Human_SNP_ID_456308188 m1A Human chr11 - 12710652 12710629 12710652 TTCACTGCTGTCCCAGTGCCTACAACAGTGTCATCCCAGTGCCTACAACAGTGTCTGGCCAGTGC TTCACTGCTGTCCCAGTGCCTACAACAGTGTC_______________________TGGCCAGTGC AGACACTGTTGTAGGCACTGGGAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:12710647..12710947 26863196 MeRIP-seq:(Medium) rs941609823 Functional Loss DEL dbSNP153 33..55 33 - - - 58273 RMVar_ID_58273 Human_SNP_ID_456308193 m1A Human chr11 - 12710652 12710652 12710652 TTCACTGCTGTCCCAGTGCCTACAACAGTGTCATCCCAGTGCCTACAACAGTGTCTGGCCAGTGC TTCACTGCTGTCCCAGTGCCTACAACAGTGTCGTCCCAGTGCCTACAACAGTGTCTGGCCAGTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:12710647..12710947 26863196 MeRIP-seq:(Medium) rs376610573 Functional Loss SNV dbSNP153 33..33 33 - - - 58274 RMVar_ID_58274 Human_SNP_ID_456324746 m1A Human chr11 - 12776004 12776004 12776004 AAACACCCCTGCACCCCTCCCTGCCCACTGTGACCCTGCCGTAACTTCCCCGGGTGAACCCCCCG AAACACCCCTGCACCCCTCCCTGCCCACTGTGCCCCTGCCGTAACTTCCCCGGGTGAACCCCCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12775996..12776095 26863196 MeRIP-seq:(Medium) rs967634351 Functional Loss SNV dbSNP153 33..33 33 - - - 58275 RMVar_ID_58275 Human_SNP_ID_456326926 m1A Human chr11 - 12783768 12783768 12783768 CACATGCTTACCAGCCTCCTTACTACTCCTGAAAACACTGTATTTTCACATCTCTCTGCCTTCAG CACATGCTTACCAGCCTCCTTACTACTCCTGAGAACACTGTATTTTCACATCTCTCTGCCTTCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12783764..12783873 26863196 MeRIP-seq:(Medium) rs1393998724 Functional Loss SNV dbSNP153 33..33 33 - - - 58276 RMVar_ID_58276 Human_SNP_ID_456327012 m1A Human chr11 + 12784092 12784090 12784093 CTTGAACTAGGTCAGAGGTTATGGGAGTGACAAGGAGGGGATGGATGGGAAGGACATTTTACATC CTTGAACTAGGTCAGAGGTTATGGGAGTGAC___GAGGGGATGGATGGGAAGGACATTTTACATC CAAG C TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12784088..12784190 26863196 MeRIP-seq:(Medium) rs1253689100 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_90079,RMVar_hsa_circ_81333,RMVar_hsa_circ_109654,RMVar_hsa_circ_10471,RMVar_hsa_circ_148280,RMVar_hsa_circ_148281,RMVar_hsa_circ_315627,RMVar_hsa_circ_59598,RMVar_hsa_circ_319151,RMVar_hsa_circ_371690,RMVar_hsa_circ_375707,RMVar_hsa_circ_328680,RMVar_hsa_circ_96327,RMVar_hsa_circ_93021,RMVar_hsa_circ_148284,RMVar_hsa_circ_148288,RMVar_hsa_circ_77799,RMVar_hsa_circ_81685,RMVar_hsa_circ_148290,RMVar_hsa_circ_148291,RMVar_hsa_circ_148289,RMVar_hsa_circ_148286,RMVar_hsa_circ_148287,RMVar_hsa_circ_148285,RMVar_hsa_circ_148283 58277 RMVar_ID_58277 Human_SNP_ID_456338732 m1A Human chr11 + 12829955 12829955 12829955 GAGTTCATAGCTGTCCATAGAGCAGGGCAGGGACATTTCTGAGAAGGTCAGAGAGGTTTGATGAG GAGTTCATAGCTGTCCATAGAGCAGGGCAGGGGCATTTCTGAGAAGGTCAGAGAGGTTTGATGAG A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12829952..12830153 26863196 MeRIP-seq:(Medium) rs946769104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90079,RMVar_hsa_circ_81333,RMVar_hsa_circ_109654,RMVar_hsa_circ_10471,RMVar_hsa_circ_148280,RMVar_hsa_circ_148281,RMVar_hsa_circ_315627,RMVar_hsa_circ_59598,RMVar_hsa_circ_319151,RMVar_hsa_circ_371690,RMVar_hsa_circ_375707,RMVar_hsa_circ_328680,RMVar_hsa_circ_96327,RMVar_hsa_circ_93021,RMVar_hsa_circ_148284,RMVar_hsa_circ_148288,RMVar_hsa_circ_77799,RMVar_hsa_circ_81685,RMVar_hsa_circ_148290,RMVar_hsa_circ_148291,RMVar_hsa_circ_148289,RMVar_hsa_circ_148286,RMVar_hsa_circ_148287,RMVar_hsa_circ_148285,RMVar_hsa_circ_148283 58278 RMVar_ID_58278 Human_SNP_ID_456344630 m1A Human chr11 - 12851950 12851950 12851950 GTAACCTCAAGTACTGAGCATGCACCCCTGCTACTGCTGCACTGCCATTACTTATCTACAGACTA GTAACCTCAAGTACTGAGCATGCACCCCTGCTTCTGCTGCACTGCCATTACTTATCTACAGACTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12851943..12852122 26863196 MeRIP-seq:(Medium) rs1461395863 Functional Loss SNV dbSNP153 33..33 33 - - - 58279 RMVar_ID_58279 Human_SNP_ID_456360067 m1A Human chr11 + 12910078 12910078 12910078 GCATTGAGATTCAGGCAGATGGATTGCCAGTGACGTGGCAGACAGTGCAATTAATGTAACAAAAT GCATTGAGATTCAGGCAGATGGATTGCCAGTGTCGTGGCAGACAGTGCAATTAATGTAACAAAAT A T TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12910030..12910113 26863196 MeRIP-seq:(Medium) rs181518633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90079,RMVar_hsa_circ_371690,RMVar_hsa_circ_567,RMVar_hsa_circ_148284,RMVar_hsa_circ_81685,RMVar_hsa_circ_148285,RMVar_hsa_circ_148283,RMVar_hsa_circ_55572,RMVar_hsa_circ_3635,RMVar_hsa_circ_352297,RMVar_hsa_circ_123922,RMVar_hsa_circ_148296,RMVar_hsa_circ_49767,RMVar_hsa_circ_359039,RMVar_hsa_circ_148299 58280 RMVar_ID_58280 Human_SNP_ID_456364305 m1A Human chr11 + 12926742 12926742 12926742 GAGCAGCCACTAGCCCTAGGATAAGTAGAGGGAGACATAAACAGAAGAACAGAGGACAAAAATGA GAGCAGCCACTAGCCCTAGGATAAGTAGAGGGGGACATAAACAGAAGAACAGAGGACAAAAATGA A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12926739..12926858 26863196 MeRIP-seq:(Medium) rs144849884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90079,RMVar_hsa_circ_371690,RMVar_hsa_circ_148284,RMVar_hsa_circ_148283,RMVar_hsa_circ_55572,RMVar_hsa_circ_123922,RMVar_hsa_circ_49767,RMVar_hsa_circ_148299,RMVar_hsa_circ_305665,RMVar_hsa_circ_148301 58281 RMVar_ID_58281 Human_SNP_ID_456364306 m1A Human chr11 + 12926742 12926742 12926742 GAGCAGCCACTAGCCCTAGGATAAGTAGAGGGAGACATAAACAGAAGAACAGAGGACAAAAATGA GAGCAGCCACTAGCCCTAGGATAAGTAGAGGGTGACATAAACAGAAGAACAGAGGACAAAAATGA A T TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12926739..12926858 26863196 MeRIP-seq:(Medium) rs144849884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90079,RMVar_hsa_circ_371690,RMVar_hsa_circ_148284,RMVar_hsa_circ_148283,RMVar_hsa_circ_55572,RMVar_hsa_circ_123922,RMVar_hsa_circ_49767,RMVar_hsa_circ_148299,RMVar_hsa_circ_305665,RMVar_hsa_circ_148301 58282 RMVar_ID_58282 Human_SNP_ID_456368230 m1A Human chr11 + 12942652 12942652 12942652 TTTCTTTTCCATTCAAATGACAGTGCGCACTTATCTGGTTTACACAATGATACCATTTTGAAAGT TTTCTTTTCCATTCAAATGACAGTGCGCACTTGTCTGGTTTACACAATGATACCATTTTGAAAGT A G TEAD1 Ensembl:ENSG00000187079 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:12942601..12942675 26863196 MeRIP-seq:(Medium) rs1281888035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31827,Human_RBP_ID_6055144,Human_RBP_ID_11560002,Human_RBP_ID_17231438,Human_RBP_ID_26603188,Human_RBP_ID_27410141 Human_miRNA_ID_644414,Human_miRNA_ID_1778037 RMVar_hsa_circ_90079,RMVar_hsa_circ_148283,RMVar_hsa_circ_123922,RMVar_hsa_circ_148299 58283 RMVar_ID_58283 Human_SNP_ID_456376363 m1A Human chr11 + 12976847 12976847 12976847 ACTCAAACTTTCCCCATCTTATCTCCCAGCATACTTGTATATAGCCATGACCTACCTACTCATGG ACTCAAACTTTCCCCATCTTATCTCCCAGCATGCTTGTATATAGCCATGACCTACCTACTCATGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:12976820..12976998 26863196 MeRIP-seq:(Medium) rs752705071 Functional Loss SNV dbSNP153 33..33 33 - - - 58284 RMVar_ID_58284 Human_SNP_ID_456376382 m1A Human chr11 - 12976925 12976925 12976925 AATGAAGGGGAGAAGACCATGCCTGGCAGTGGAGAGAGCACAAGCAGAAGGTGGGAAAGCGTGTG AATGAAGGGGAGAAGACCATGCCTGGCAGTGGGGAGAGCACAAGCAGAAGGTGGGAAAGCGTGTG T C LINC00958 Ensembl:ENSG00000251381 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:12976762..12977083 26863196 MeRIP-seq:(Medium) rs1031930076 Functional Loss SNV dbSNP153 33..33 33 - - - 58285 RMVar_ID_58285 Human_SNP_ID_456453174 m1A Human chr11 - 13277909 13277909 13277909 CGCCGGCCTGACACTCACCGTGGCTCGCCGGGAGCGCCCGCGCCCGCGCCCGCACTCGGATCCCG CGCCGGCCTGACACTCACCGTGGCTCGCCGGGCGCGCCCGCGCCCGCGCCCGCACTCGGATCCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:13277744..13277953 26863196 MeRIP-seq:(Medium) rs929502590 Functional Loss SNV dbSNP153 33..33 33 - - - 58286 RMVar_ID_58286 Human_SNP_ID_456461373 m1A Human chr11 + 13309948 13309948 13309948 GGAGTATGGTAAATCAAAACTTATTGGGTGCTATGAATTTAAAGCTAAACTTTTATTTCATTGGC GGAGTATGGTAAATCAAAACTTATTGGGTGCTGTGAATTTAAAGCTAAACTTTTATTTCATTGGC A G ARNTL Ensembl:ENSG00000133794 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:13309940..13310083 26863196 MeRIP-seq:(Medium) rs535029061 Functional Loss SNV dbSNP153 33..33 33 - - - 58287 RMVar_ID_58287 Human_SNP_ID_456552364 m1A Human chr11 + 13668733 13668733 13668733 CGGGCGGTGGAAAAGCGAGTGAAGAGAGCGCGACGGCGGCGGCGGCGGCGGCGCAGCTATTGCTG CGGGCGGTGGAAAAGCGAGTGAAGAGAGCGCGGCGGCGGCGGCGGCGGCGGCGCAGCTATTGCTG A G FAR1 Ensembl:ENSG00000197601 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:13668695..13694825;chr11:13668703..13694768 26863196 MeRIP-seq:(Medium) rs376260899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227307,Human_RBP_ID_392498,Human_RBP_ID_4184675,Human_RBP_ID_11567598,Human_RBP_ID_26319620,Human_RBP_ID_27803254 Human_Splice_Rec_1212689,Human_Splice_Rec_1212709 RMVar_hsa_circ_86150,RMVar_hsa_circ_148324 58288 RMVar_ID_58288 Human_SNP_ID_456552534 m1A Human chr11 - 13669092 13669092 13669092 CACCTTCGCCACCTCTAGCGGCCTCCCACCCCAGGCGGCTCCCCGGGCTCCGCGGCTGCAAACCA CACCTTCGCCACCTCTAGCGGCCTCCCACCCCGGGCGGCTCCCCGGGCTCCGCGGCTGCAAACCA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:13669088..13669294 26863196 MeRIP-seq:(Medium) rs1465312006 Functional Loss SNV dbSNP153 33..33 33 - - - 58289 RMVar_ID_58289 Human_SNP_ID_456704885 m1A Human chr11 - 14281700 14281700 14281700 TTGGAATTTCAGGTAACACAGGAAGAAGGACAACAGTTAGCACGGCAGCTTAAGGTAACATACAT TTGGAATTTCAGGTAACACAGGAAGAAGGACAGCAGTTAGCACGGCAGCTTAAGGTAACATACAT T C RRAS2 Ensembl:ENSG00000133818 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:14281652..14281751 26863196 MeRIP-seq:(Medium) rs782747533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6058143,Human_RBP_ID_11570170 Human_Splice_Rec_1212858,Human_Splice_Rec_1212859,Human_Splice_Rec_1212868,Human_Splice_Rec_1212869,Human_Splice_Rec_1212876,Human_Splice_Rec_1212877,Human_Splice_Rec_1212886,Human_Splice_Rec_1212887,Human_Splice_Rec_1212896,Human_Splice_Rec_1212897,Human_Splice_Rec_1212906,Human_Splice_Rec_1212907,Human_Splice_Rec_1212916,Human_Splice_Rec_1212917,Human_Splice_Rec_1212926,Human_Splice_Rec_1212927,Human_Splice_Rec_1212938,Human_Splice_Rec_1212946 RMVar_hsa_circ_25591 58290 RMVar_ID_58290 Human_SNP_ID_456724340 m1A Human chr11 - 14359037 14359037 14359037 TCCGCGCCTCGGGCGGTACCCAGCCAGTCCCCAGCGCCGCGCTACCGCGCTGACCGGCCCTCCAG TCCGCGCCTCGGGCGGTACCCAGCCAGTCCCCGGCGCCGCGCTACCGCGCTGACCGGCCCTCCAG T C RRAS2 Ensembl:ENSG00000133818 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:14358282..14359175 26863196 MeRIP-seq:(Medium) rs1447096587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184676,Human_RBP_ID_5436231,Human_RBP_ID_9321322,Human_RBP_ID_18477629 58291 RMVar_ID_58291 Human_SNP_ID_456724372 m1A Human chr11 + 14359102 14359102 14359102 GAAGCGGGGTGACGGCACGGGCCAGGGGCGGCAGCGGCCGGGGGGCGCGCTCCTCTACGCGTCTC GAAGCGGGGTGACGGCACGGGCCAGGGGCGGCTGCGGCCGGGGGGCGCGCTCCTCTACGCGTCTC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:14359001..14359175 26863410 MeRIP-seq:(Medium) rs1456287401 Functional Loss SNV dbSNP153 33..33 33 - - - 58292 RMVar_ID_58292 Human_SNP_ID_456751595 m1A Human chr11 + 14476886 14476886 14476886 AAAAGTCAGATTTTCCTAAAGGAAAAATTACCATATAAACTAACATTTACTAAAGTAAAACATAC AAAAGTCAGATTTTCCTAAAGGAAAAATTACCGTATAAACTAACATTTACTAAAGTAAAACATAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:14476882..14476953 26863196 MeRIP-seq:(Medium) rs1357005900 Functional Loss SNV dbSNP153 33..33 33 - - - 58293 RMVar_ID_58293 Human_SNP_ID_456757481 m1A Human chr11 - 14499783 14499783 14499783 GTTCATAGCCGGAGTAGACGGAGCCGCAGTAGACGGATCCGCGGCTGCACCAAACCACTGCCCCT GTTCATAGCCGGAGTAGACGGAGCCGCAGTAGGCGGATCCGCGGCTGCACCAAACCACTGCCCCT T C AC018523.2,COPB1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129083 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:14499629..14499825 26863196 MeRIP-seq:(Medium) rs1000195250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807796,Human_RBP_ID_4183957,Human_RBP_ID_8773381,Human_RBP_ID_8940529,Human_RBP_ID_9254549,Human_RBP_ID_9275486,Human_RBP_ID_9321324,Human_RBP_ID_17350039,Human_RBP_ID_18416520,Human_RBP_ID_22895006,Human_RBP_ID_23117941,Human_RBP_ID_26775586 Human_Splice_Rec_1213009,Human_Splice_Rec_1213055,Human_Splice_Rec_1213095,Human_Splice_Rec_1213101 Human_miRNA_ID_1983415,Human_miRNA_ID_3114551 RMVar_hsa_circ_148334,RMVar_hsa_circ_93534,RMVar_hsa_circ_148345,RMVar_hsa_circ_148344 58294 RMVar_ID_58294 Human_SNP_ID_456759795 m1A Human chr11 - 14508809 14508809 14508809 AACTTTCAAGGAGGAGGGGCAATGAAGTTGTCACTGAGGACCTGACAAAACAGGCTTAATGGAAT AACTTTCAAGGAGGAGGGGCAATGAAGTTGTCGCTGAGGACCTGACAAAACAGGCTTAATGGAAT T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:14508781..14508910 26863196 MeRIP-seq:(Medium) rs1363412576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11572451 RMVar_hsa_circ_148334,RMVar_hsa_circ_3278,RMVar_hsa_circ_148345,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349,RMVar_hsa_circ_148350,RMVar_hsa_circ_297712,RMVar_hsa_circ_357707,RMVar_hsa_circ_18949 58295 RMVar_ID_58295 Human_SNP_ID_456760341 m1A Human chr11 - 14510904 14510904 14510904 TAGTTAAACATGGTCTGCGTGCCTTAAGAGAGACGCTTCCTGCAGAACAGGACCTGACTACAAAG TAGTTAAACATGGTCTGCGTGCCTTAAGAGAGGCGCTTCCTGCAGAACAGGACCTGACTACAAAG T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding 3'UTR,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1264477923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_392760,Human_RBP_ID_6058632,Human_RBP_ID_9001511,Human_RBP_ID_11572494,Human_RBP_ID_18971753,Human_RBP_ID_22792658,Human_RBP_ID_23495894,Human_RBP_ID_26888099,Human_RBP_ID_27199819 Human_Splice_Rec_1213118,Human_Splice_Rec_1213119,Human_Splice_Rec_1213129,Human_Splice_Rec_1213146,Human_Splice_Rec_1213147,Human_Splice_Rec_1213164,Human_Splice_Rec_1213165,Human_Splice_Rec_1213178,Human_Splice_Rec_1213179,Human_Splice_Rec_1213196,Human_Splice_Rec_1213197,Human_Splice_Rec_1213202,Human_Splice_Rec_1213203,Human_Splice_Rec_1213208 Human_miRNA_ID_1979059 RMVar_hsa_circ_148334,RMVar_hsa_circ_3278,RMVar_hsa_circ_148345,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349,RMVar_hsa_circ_72093,RMVar_hsa_circ_148350,RMVar_hsa_circ_297712,RMVar_hsa_circ_357707,RMVar_hsa_circ_18949,RMVar_hsa_circ_98278,RMVar_hsa_circ_375209,RMVar_hsa_circ_148351,RMVar_hsa_circ_148352 58296 RMVar_ID_58296 Human_SNP_ID_456762088 m1A Human chr11 - 14517983 14517983 14517983 TAAGATGTGTGTTTTTTGTTTTTTTTTTCTTTAGGGCAGGATTCATCAAATTGAATATGCAATGG TAAGATGTGTGTTTTTTGTTTTTTTTTTCTTTTGGGCAGGATTCATCAAATTGAATATGCAATGG T A AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:14517934..14518025;chr11:14517951..14518000 26863196 MeRIP-seq:(Medium) rs755407938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864836,Human_RBP_ID_6058688,Human_RBP_ID_22640979,Human_RBP_ID_22895290 RMVar_hsa_circ_3278,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349,RMVar_hsa_circ_125571,RMVar_hsa_circ_18949,RMVar_hsa_circ_98278,RMVar_hsa_circ_148352,RMVar_hsa_circ_148353 58297 RMVar_ID_58297 Human_SNP_ID_456764000 m1A Human chr11 - 14525658 14525657 14525659 AGTGAGTTGTGGAGGAAGGTATTGAGGACAAAAGAGTGTACGGGTTGCGCACTACAGGGTGGATA AGTGAGTTGTGGAGGAAGGTATTGAGGACAA__GAGTGTACGGGTTGCGCACTACAGGGTGGATA CTT C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:14525623..14525769 26863196 MeRIP-seq:(Medium) rs753230343 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 58298 RMVar_ID_58298 Human_SNP_ID_456764001 m1A Human chr11 - 14525661 14525661 14525661 AATAGTGAGTTGTGGAGGAAGGTATTGAGGACAAAAGAGTGTACGGGTTGCGCACTACAGGGTGG AATAGTGAGTTGTGGAGGAAGGTATTGAGGACGAAAGAGTGTACGGGTTGCGCACTACAGGGTGG T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:14525631..14525740 26863196 MeRIP-seq:(Medium) rs767435088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 58299 RMVar_ID_58299 Human_SNP_ID_456778260 m1A Human chr11 - 14588991 14588991 14588991 AAGAAGGGTGAATGCCTAAAGGAGGGTAAGTAAAAGGAAGGGTAGTAAGAAGTGAAGTGCCAGAA AAGAAGGGTGAATGCCTAAAGGAGGGTAAGTAGAAGGAAGGGTAGTAAGAAGTGAAGTGCCAGAA T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:14588890..14589109 26863196 MeRIP-seq:(Medium) rs753414462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 58300 RMVar_ID_58300 Human_SNP_ID_456792108 m1A Human chr11 - 14643603 14643603 14643603 GCGGCCGCCCAACAGGGACGCGAGCCGGGACCACGCCGACCCAGCGTGCCCAGGCCGAGGAAAGC GCGGCCGCCCAACAGGGACGCGAGCCGGGACCCCGCCGACCCAGCGTGCCCAGGCCGAGGAAAGC T G PSMA1 Ensembl:ENSG00000129084 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:14643507..14643611 26863196 MeRIP-seq:(Medium) rs528715813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4189270 58301 RMVar_ID_58301 Human_SNP_ID_456792298 m1A Human chr11 - 14644025 14644025 14644025 CCACGGGACTCAGCACACCCCGCTCGTACCGTAGCGGCCGCTCGCGCTCCCAGACCCCAACCCCC CCACGGGACTCAGCACACCCCGCTCGTACCGTGGCGGCCGCTCGCGCTCCCAGACCCCAACCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:14643745..14644198 26863196 MeRIP-seq:(Medium) rs1463073270 Functional Loss SNV dbSNP153 33..33 33 - - - 58302 RMVar_ID_58302 Human_SNP_ID_456814925 m1A Human chr11 + 14731975 14731975 14731975 AAATTAAGCAAGGAAGGGTAAAGGGGAATTCTAGGGGTTAGGAAAGGGGAGTTATAATTTTAAAC AAATTAAGCAAGGAAGGGTAAAGGGGAATTCTTGGGGTTAGGAAAGGGGAGTTATAATTTTAAAC A T PDE3B Ensembl:ENSG00000152270 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:14731974..14732113 26863196 MeRIP-seq:(Medium) rs995580646 Functional Loss SNV dbSNP153 33..33 33 - - - 58303 RMVar_ID_58303 Human_SNP_ID_456832999 m1A Human chr11 - 14807549 14807549 14807549 CTTTTCTTTTCTCAGATTCTTTTGAATTATTCAAGCTTTTTTTAATCATGCCATTTTACCTCCTT CTTTTCTTTTCTCAGATTCTTTTGAATTATTCCAGCTTTTTTTAATCATGCCATTTTACCTCCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:14807538..14807643 26863196 MeRIP-seq:(Medium) rs574152556 Functional Loss SNV dbSNP153 33..33 33 - - - 58304 RMVar_ID_58304 Human_SNP_ID_457291820 m1A Human chr11 + 16748126 16748126 16748126 TAGAAAGAACATACTGGTCGTCTTGTTATAGGAGATCACAAATCAACATCTCACTTCCGAACCGG TAGAAAGAACATACTGGTCGTCTTGTTATAGGTGATCACAAATCAACATCTCACTTCCGAACCGG A T C11orf58 Ensembl:ENSG00000110696 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:16748101..16748125 26863196 MeRIP-seq:(Medium) rs1224501997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1455438,Human_RBP_ID_1777406,Human_RBP_ID_3371933,Human_RBP_ID_6059676,Human_RBP_ID_9362035,Human_RBP_ID_11575054,Human_RBP_ID_17231567,Human_RBP_ID_17348005,Human_RBP_ID_17464000,Human_RBP_ID_17793032,Human_RBP_ID_22420690,Human_RBP_ID_22790022,Human_RBP_ID_22889890,Human_RBP_ID_26317771,Human_RBP_ID_27803262 Human_Splice_Rec_1214026,Human_Splice_Rec_1214028,Human_Splice_Rec_1214029,Human_Splice_Rec_1214036,Human_Splice_Rec_1214037,Human_Splice_Rec_1214044,Human_Splice_Rec_1214045,Human_Splice_Rec_1214060,Human_Splice_Rec_1214062,Human_Splice_Rec_1214063 RMVar_hsa_circ_1071,RMVar_hsa_circ_358044 58305 RMVar_ID_58305 Human_SNP_ID_457336270 m1A Human chr11 - 16925825 16925823 16925825 TGGGCTCGGACGCGCCGTCCTGGCCGAACGGCAGCACCTGGGGCGCGCTCTGGACCGCTGGGGTC TGGGCTCGGACGCGCCGTCCTGGCCGAACGGC__CACCTGGGGCGCGCTCTGGACCGCTGGGGTC GCT G PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:16925720..16925853 26863196 MeRIP-seq:(Medium) rs1565122952 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58306 RMVar_ID_58306 Human_SNP_ID_457344249 m1A Human chr11 - 16960132 16960132 16960132 GGGGCCCCTGAAAGGAACGTGGCCTAAAGTGGAGAGTGAAGCCGGAGCAGAGCAGGGCGTGAGAA GGGGCCCCTGAAAGGAACGTGGCCTAAAGTGGGGAGTGAAGCCGGAGCAGAGCAGGGCGTGAGAA T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:16960130..16960224 26863196 MeRIP-seq:(Medium) rs980256324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58307 RMVar_ID_58307 Human_SNP_ID_457347365 m1A Human chr11 - 16973805 16973805 16973805 ACAGGGCCTTTCATGTTTGATACTCACAGTGGATGGGGAGGAACACTCCAGAGGGAGACTCAGGT ACAGGGCCTTTCATGTTTGATACTCACAGTGGTTGGGGAGGAACACTCCAGAGGGAGACTCAGGT T A PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:16973803..16973955 26863196 MeRIP-seq:(Medium) rs114459117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58308 RMVar_ID_58308 Human_SNP_ID_457347366 m1A Human chr11 - 16973805 16973805 16973805 ACAGGGCCTTTCATGTTTGATACTCACAGTGGATGGGGAGGAACACTCCAGAGGGAGACTCAGGT ACAGGGCCTTTCATGTTTGATACTCACAGTGGGTGGGGAGGAACACTCCAGAGGGAGACTCAGGT T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:16973803..16973955 26863196 MeRIP-seq:(Medium) rs114459117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58309 RMVar_ID_58309 Human_SNP_ID_457347654 m1A Human chr11 - 16974902 16974902 16974902 AGAAGGGCAAGGATTCTCTGTACGCCCAGGGAAAGCGGCGTTATGACAGGAAGCAGAGTGGCTAT AGAAGGGCAAGGATTCTCTGTACGCCCAGGGACAGCGGCGTTATGACAGGAAGCAGAGTGGCTAT T G PLEKHA7,AC116533.1 Ensembl:ENSG00000166689,Ensembl:ENSG00000244398 Protein coding,Pseudogene intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:16974868..16974943 26863196 MeRIP-seq:(Medium) rs1316186486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_392994,Human_RBP_ID_1063917,Human_RBP_ID_1455491,Human_RBP_ID_1777449,Human_RBP_ID_3372001,Human_RBP_ID_4155155,Human_RBP_ID_5093002,Human_RBP_ID_5169028,Human_RBP_ID_6059963,Human_RBP_ID_8347972,Human_RBP_ID_9001640,Human_RBP_ID_11575712,Human_RBP_ID_17233887,Human_RBP_ID_17673002,Human_RBP_ID_17682985,Human_RBP_ID_17804481,Human_RBP_ID_18605708,Human_RBP_ID_18926281,Human_RBP_ID_22160267,Human_RBP_ID_22369738,Human_RBP_ID_22790031,Human_RBP_ID_26410384,Human_RBP_ID_26803269,Human_RBP_ID_26888415,Human_RBP_ID_27199969 RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58310 RMVar_ID_58310 Human_SNP_ID_457349923 m1A Human chr11 - 16984490 16984490 16984490 CGAGGAAACAGCAAGGAGGCCAGAGTGGATGGAGCTCAGGGAGTAGGAGTTGAGACTGGAGAGGT CGAGGAAACAGCAAGGAGGCCAGAGTGGATGGCGCTCAGGGAGTAGGAGTTGAGACTGGAGAGGT T G PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:16984487..16984713 26863196 MeRIP-seq:(Medium) rs1046420238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58311 RMVar_ID_58311 Human_SNP_ID_457356487 m1A Human chr11 - 17012003 17012003 17012003 CAGGGAGTAGTGGTCACATTCAGGCTGTGTTTAGGAAATAGGCTCTTCACACCTTCATGATGGAC CAGGGAGTAGTGGTCACATTCAGGCTGTGTTTGGGAAATAGGCTCTTCACACCTTCATGATGGAC T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:17012001..17012457 26863196 MeRIP-seq:(Medium) rs915507816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113097,RMVar_hsa_circ_82968,RMVar_hsa_circ_148418,RMVar_hsa_circ_148417,RMVar_hsa_circ_10701 58312 RMVar_ID_58312 Human_SNP_ID_457357208 m1A Human chr11 + 17014151 17014151 17014151 GCCCACCTGAGCGGATCATGTGGCCCGAGTTGACGGGCTCCCCGGTGCGCGGATGCAGCCAGGTC GCCCACCTGAGCGGATCATGTGGCCCGAGTTGGCGGGCTCCCCGGTGCGCGGATGCAGCCAGGTC A G OR7E14P Ensembl:ENSG00000184669 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17014022..17014227 26863196 MeRIP-seq:(Medium) rs1174487472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185648 58313 RMVar_ID_58313 Human_SNP_ID_457357359 m1A Human chr11 - 17014374 17014374 17014374 CGAACATGGCGGCGGCGACGGTCGGGCGGGACACTTTACCTGAGCATTGGTCCTACGGGGTGTGC CGAACATGGCGGCGGCGACGGTCGGGCGGGACGCTTTACCTGAGCATTGGTCCTACGGGGTGTGC T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:17013973..17014378 26863196 MeRIP-seq:(Medium) rs940541538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17793091 Human_Splice_Rec_1214071,Human_Splice_Rec_1214195,Human_Splice_Rec_1214323 RMVar_hsa_circ_82968,RMVar_hsa_circ_148417 58314 RMVar_ID_58314 Human_SNP_ID_457357360 m1A Human chr11 - 17014374 17014374 17014374 CGAACATGGCGGCGGCGACGGTCGGGCGGGACACTTTACCTGAGCATTGGTCCTACGGGGTGTGC CGAACATGGCGGCGGCGACGGTCGGGCGGGACCCTTTACCTGAGCATTGGTCCTACGGGGTGTGC T G PLEKHA7 Ensembl:ENSG00000166689 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:17013973..17014378 26863196 MeRIP-seq:(Medium) rs940541538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17793091 Human_Splice_Rec_1214071,Human_Splice_Rec_1214195,Human_Splice_Rec_1214323 RMVar_hsa_circ_82968,RMVar_hsa_circ_148417 58315 RMVar_ID_58315 Human_SNP_ID_457357362 m1A Human chr11 - 17014376 17014376 17014376 GGCGAACATGGCGGCGGCGACGGTCGGGCGGGACACTTTACCTGAGCATTGGTCCTACGGGGTGT GGCGAACATGGCGGCGGCGACGGTCGGGCGGGGCACTTTACCTGAGCATTGGTCCTACGGGGTGT T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:17014294..17052059 26863196 MeRIP-seq:(Medium) rs1037277652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17793091 Human_Splice_Rec_1214071,Human_Splice_Rec_1214195,Human_Splice_Rec_1214323 RMVar_hsa_circ_82968,RMVar_hsa_circ_148417 58316 RMVar_ID_58316 Human_SNP_ID_457373426 m1A Human chr11 - 17075168 17075168 17075168 TAGGATAAGGATGCTAAATTCCGTCTGATTCTAATAGAGAGCCGGATTCACCGTTTGGCTCGATA TAGGATAAGGATGCTAAATTCCGTCTGATTCTGATAGAGAGCCGGATTCACCGTTTGGCTCGATA T C RPS13 Ensembl:ENSG00000110700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17075117..17075267 32194978 MeRIP-seq:(Medium) rs1059640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29989,Human_RBP_ID_393020,Human_RBP_ID_748742,Human_RBP_ID_986480,Human_RBP_ID_1455511,Human_RBP_ID_1777460,Human_RBP_ID_2261461,Human_RBP_ID_3372027,Human_RBP_ID_4155179,Human_RBP_ID_6060123,Human_RBP_ID_8348006,Human_RBP_ID_9001648,Human_RBP_ID_11576495,Human_RBP_ID_17231583,Human_RBP_ID_17348028,Human_RBP_ID_17464027,Human_RBP_ID_17793104,Human_RBP_ID_18249185,Human_RBP_ID_18605727,Human_RBP_ID_23496823,Human_RBP_ID_24459296,Human_RBP_ID_27199981,Human_RBP_ID_27410452,Human_RBP_ID_27616351 Human_Splice_Rec_1214396,Human_Splice_Rec_1214397,Human_Splice_Rec_1214399,Human_Splice_Rec_1214402,Human_Splice_Rec_1214403,Human_Splice_Rec_1214413,Human_Splice_Rec_1214422,Human_Splice_Rec_1214423,Human_Splice_Rec_1214430,Human_Splice_Rec_1214431 RMVar_hsa_circ_35996,RMVar_hsa_circ_110321,RMVar_hsa_circ_127941,RMVar_hsa_circ_80997,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148441,RMVar_hsa_circ_148442,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698 58317 RMVar_ID_58317 Human_SNP_ID_457373427 m1A Human chr11 - 17075168 17075168 17075168 TAGGATAAGGATGCTAAATTCCGTCTGATTCTAATAGAGAGCCGGATTCACCGTTTGGCTCGATA TAGGATAAGGATGCTAAATTCCGTCTGATTCTCATAGAGAGCCGGATTCACCGTTTGGCTCGATA T G RPS13 Ensembl:ENSG00000110700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17075117..17075267 32194978 MeRIP-seq:(Medium) rs1059640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29989,Human_RBP_ID_393020,Human_RBP_ID_748742,Human_RBP_ID_986480,Human_RBP_ID_1455511,Human_RBP_ID_1777460,Human_RBP_ID_2261461,Human_RBP_ID_3372027,Human_RBP_ID_4155179,Human_RBP_ID_6060123,Human_RBP_ID_8348006,Human_RBP_ID_9001648,Human_RBP_ID_11576495,Human_RBP_ID_17231583,Human_RBP_ID_17348028,Human_RBP_ID_17464027,Human_RBP_ID_17793104,Human_RBP_ID_18249185,Human_RBP_ID_18605727,Human_RBP_ID_23496823,Human_RBP_ID_24459296,Human_RBP_ID_27199981,Human_RBP_ID_27410452,Human_RBP_ID_27616351 Human_Splice_Rec_1214396,Human_Splice_Rec_1214397,Human_Splice_Rec_1214399,Human_Splice_Rec_1214402,Human_Splice_Rec_1214403,Human_Splice_Rec_1214413,Human_Splice_Rec_1214422,Human_Splice_Rec_1214423,Human_Splice_Rec_1214430,Human_Splice_Rec_1214431 RMVar_hsa_circ_35996,RMVar_hsa_circ_110321,RMVar_hsa_circ_127941,RMVar_hsa_circ_80997,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148441,RMVar_hsa_circ_148442,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698 58318 RMVar_ID_58318 Human_SNP_ID_457373879 m1A Human chr11 - 17076680 17076680 17076680 AAAAAAGCCAGCCGCAATGTGCCTGTAGTCCCAGATACTTGGGATGCAGAGGTGAGAGGATCACC AAAAAAGCCAGCCGCAATGTGCCTGTAGTCCCGGATACTTGGGATGCAGAGGTGAGAGGATCACC T C RPS13 Ensembl:ENSG00000110700 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17076677..17076742 26863196 MeRIP-seq:(Medium) rs901708003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11576558 RMVar_hsa_circ_110321,RMVar_hsa_circ_127941,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148441,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698,RMVar_hsa_circ_48535 58319 RMVar_ID_58319 Human_SNP_ID_457374110 m1A Human chr11 - 17077463 17077463 17077463 GACTGCTTCTCTCCCCAGGAAGGGCCTGTCCCAGTCGGCTTTACCCTATCGACGCAGCGTCCCCA GACTGCTTCTCTCCCCAGGAAGGGCCTGTCCCTGTCGGCTTTACCCTATCGACGCAGCGTCCCCA T A RPS13 Ensembl:ENSG00000110700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17077426..17077539 32194978 MeRIP-seq:(Medium) rs778376279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226434,Human_RBP_ID_393032,Human_RBP_ID_748747,Human_RBP_ID_869373,Human_RBP_ID_1455523,Human_RBP_ID_4155195,Human_RBP_ID_5341229,Human_RBP_ID_17350060,Human_RBP_ID_17793109,Human_RBP_ID_18417081,Human_RBP_ID_18605738,Human_RBP_ID_19051121,Human_RBP_ID_22432818,Human_RBP_ID_22471135,Human_RBP_ID_22568747,Human_RBP_ID_22644078,Human_RBP_ID_26767883 Human_Splice_Rec_1214390,Human_Splice_Rec_1214391,Human_Splice_Rec_1214406,Human_Splice_Rec_1214407,Human_Splice_Rec_1214416,Human_Splice_Rec_1214417,Human_Splice_Rec_1214425,Human_Splice_Rec_1214434,Human_Splice_Rec_1214435,Human_Splice_Rec_1214441,Human_Splice_Rec_1214444,Human_Splice_Rec_1214445,Human_Splice_Rec_1214448 RMVar_hsa_circ_127941,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698,RMVar_hsa_circ_48535 58320 RMVar_ID_58320 Human_SNP_ID_457374111 m1A Human chr11 - 17077463 17077463 17077463 GACTGCTTCTCTCCCCAGGAAGGGCCTGTCCCAGTCGGCTTTACCCTATCGACGCAGCGTCCCCA GACTGCTTCTCTCCCCAGGAAGGGCCTGTCCCGGTCGGCTTTACCCTATCGACGCAGCGTCCCCA T C RPS13 Ensembl:ENSG00000110700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17077426..17077539 32194978 MeRIP-seq:(Medium) rs778376279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226434,Human_RBP_ID_393032,Human_RBP_ID_748747,Human_RBP_ID_869373,Human_RBP_ID_1455523,Human_RBP_ID_4155195,Human_RBP_ID_5341229,Human_RBP_ID_17350060,Human_RBP_ID_17793109,Human_RBP_ID_18417081,Human_RBP_ID_18605738,Human_RBP_ID_19051121,Human_RBP_ID_22432818,Human_RBP_ID_22471135,Human_RBP_ID_22568747,Human_RBP_ID_22644078,Human_RBP_ID_26767883 Human_Splice_Rec_1214390,Human_Splice_Rec_1214391,Human_Splice_Rec_1214406,Human_Splice_Rec_1214407,Human_Splice_Rec_1214416,Human_Splice_Rec_1214417,Human_Splice_Rec_1214425,Human_Splice_Rec_1214434,Human_Splice_Rec_1214435,Human_Splice_Rec_1214441,Human_Splice_Rec_1214444,Human_Splice_Rec_1214445,Human_Splice_Rec_1214448 RMVar_hsa_circ_127941,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698,RMVar_hsa_circ_48535 58321 RMVar_ID_58321 Human_SNP_ID_457397652 m1A Human chr11 - 17169780 17169780 17169780 GTATAGGCCTTGCTATTTTGGAAGCTACAAGAAAAAAATAGAGGAAGGAAGGTTTGGTCTTTTTA GTATAGGCCTTGCTATTTTGGAAGCTACAAGATAAAAATAGAGGAAGGAAGGTTTGGTCTTTTTA T A PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17169612..17204312 26863196 MeRIP-seq:(Medium) rs1340983326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214536,Human_Splice_Rec_1214548 RMVar_hsa_circ_8646,RMVar_hsa_circ_69091,RMVar_hsa_circ_364891,RMVar_hsa_circ_148506,RMVar_hsa_circ_373566,RMVar_hsa_circ_368928,RMVar_hsa_circ_148507,RMVar_hsa_circ_266258,RMVar_hsa_circ_342262,RMVar_hsa_circ_287206 58322 RMVar_ID_58322 Human_SNP_ID_457407646 m1A Human chr11 + 17207909 17207909 17207909 ACAACCTGAGCCGCCGAAGCCGCCACAGTCCGAGCCATTTTTCCCCTCAGCTGGCTCAGCCGCCG ACAACCTGAGCCGCCGAAGCCGCCACAGTCCGTGCCATTTTTCCCCTCAGCTGGCTCAGCCGCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:17207805..17207936;chr11:17169671..17207952;chr11:17207785..17207955 26863196 MeRIP-seq:(Medium) rs1386958303 Functional Loss SNV dbSNP153 33..33 33 - - - 58323 RMVar_ID_58323 Human_SNP_ID_457407656 m1A Human chr11 + 17207934 17207921 17207934 CAGTCCGAGCCATTTTTCCCCTCAGCTGGCTCAGCCGCCGCCGAAAGCTTCGGCCGACTCCACAG CAGTCCGAGCCATTTTTCCC_____________GCCGCCGCCGAAAGCTTCGGCCGACTCCACAG CCTCAGCTGGCTCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:17207848..17207954 26863196 MeRIP-seq:(Medium) rs1237362512 Functional Loss DEL dbSNP153 21..33 33 - - - 58324 RMVar_ID_58324 Human_SNP_ID_457424815 m1A Human chr11 - 17276776 17276776 17276776 GAGGCTGCGCCTGGTGCTTGCGTCCAGCGCACAAACCTGTCCTCCAGCCCCCGGCCCACCGCTCC GAGGCTGCGCCTGGTGCTTGCGTCCAGCGCACCAACCTGTCCTCCAGCCCCCGGCCCACCGCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:17276726..17276875;chr11:17276726..17276869;chr11:17276726..17276888 26863196 MeRIP-seq:(Medium) rs1174433840 Functional Loss SNV dbSNP153 33..33 33 - - - 58325 RMVar_ID_58325 Human_SNP_ID_457424894 m1A Human chr11 + 17277023 17277023 17277023 GCGAGCCGGAGGCGCTGGGTTCCCTCTGCTCCACTCGCAGCTGGGCACCCGAGCTTTCTTCGGGG GCGAGCCGGAGGCGCTGGGTTCCCTCTGCTCCGCTCGCAGCTGGGCACCCGAGCTTTCTTCGGGG A G NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17277018..17277146 26863196 MeRIP-seq:(Medium) rs918388433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214729,Human_Splice_Rec_1214743 58326 RMVar_ID_58326 Human_SNP_ID_457451551 m1A Human chr11 - 17388716 17388715 17388716 GGGCGGGGAGAAGGGCTCTTAGCGGGAGGCCCAGGGGTGGTCAGCTGGTGGGGGAAGCTGGGGGA GGGCGGGGAGAAGGGCTCTTAGCGGGAGGCCC_GGGGTGGTCAGCTGGTGGGGGAAGCTGGGGGA CT C KCNJ11 Ensembl:ENSG00000187486 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:17388648..17388761 26863196 MeRIP-seq:(Medium) rs1415193028 Functional Loss DEL dbSNP153 33..33 33 - - - 58327 RMVar_ID_58327 Human_SNP_ID_457451552 m1A Human chr11 - 17388716 17388716 17388716 GGGCGGGGAGAAGGGCTCTTAGCGGGAGGCCCAGGGGTGGTCAGCTGGTGGGGGAAGCTGGGGGA GGGCGGGGAGAAGGGCTCTTAGCGGGAGGCCCGGGGGTGGTCAGCTGGTGGGGGAAGCTGGGGGA T C KCNJ11 Ensembl:ENSG00000187486 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:17388648..17388761 26863196 MeRIP-seq:(Medium) rs1160904815 Functional Loss SNV dbSNP153 33..33 33 - - - 58328 RMVar_ID_58328 Human_SNP_ID_457484016 m1A Human chr11 - 17509700 17509700 17509700 TCCCTTTGGACATGTTCTACTATCCCCCCAAGACTCCCTCTGCCTTGCCTGTGATGCCCCACCCT TCCCTTTGGACATGTTCTACTATCCCCCCAAGCCTCCCTCTGCCTTGCCTGTGATGCCCCACCCT T G USH1C Ensembl:ENSG00000006611 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:17509651..17509791 26863196 MeRIP-seq:(Medium) rs768816943 Functional Loss SNV dbSNP153 33..33 33 - - - 58329 RMVar_ID_58329 Human_SNP_ID_457484079 m1A Human chr11 + 17509818 17509818 17509818 GGTGGGGCCAGGGGAGACACAGAAGGCGGGGGAGGCGGGGGCCCTGTGGTCATCTGGGGGTGTTG GGTGGGGCCAGGGGAGACACAGAAGGCGGGGGGGGCGGGGGCCCTGTGGTCATCTGGGGGTGTTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:17509577..17509850 26863196 MeRIP-seq:(Medium) rs1255408661 Functional Loss SNV dbSNP153 33..33 33 - - - 58330 RMVar_ID_58330 Human_SNP_ID_457487399 m1A Human chr11 - 17522744 17522744 17522744 CAGCCAGCCCTGGATGCCCTGTCCCGCCTCCCACCCCACCACACGACCCCACCTAGCTTGCTTCC CAGCCAGCCCTGGATGCCCTGTCCCGCCTCCCCCCCCACCACACGACCCCACCTAGCTTGCTTCC T G USH1C Ensembl:ENSG00000006611 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17522743..17522867 26863196 MeRIP-seq:(Medium) rs1322043131 Functional Loss SNV dbSNP153 33..33 33 - - - 58331 RMVar_ID_58331 Human_SNP_ID_457494044 m1A Human chr11 + 17547545 17547545 17547545 AAACGTTAAAGGAATGAGGAATGGGCCCGCGCAGGTTGGAGAGAGGGAGGAAAGAGAGGTTTGAG AAACGTTAAAGGAATGAGGAATGGGCCCGCGCCGGTTGGAGAGAGGGAGGAAAGAGAGGTTTGAG A C OTOG Ensembl:ENSG00000188162 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17547509..17547823 26863196 MeRIP-seq:(Medium) rs939488779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1217389 58332 RMVar_ID_58332 Human_SNP_ID_457494091 m1A Human chr11 + 17547706 17547706 17547706 TTAGGCTGGGTGGAAGAGACCCGAGGTGGGGAACTAGAGAGAGCTGGGGGCCAAAGACTGAGAGT TTAGGCTGGGTGGAAGAGACCCGAGGTGGGGACCTAGAGAGAGCTGGGGGCCAAAGACTGAGAGT A C OTOG Ensembl:ENSG00000188162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:17547519..17547802 26863196 MeRIP-seq:(Medium) rs1221811246 Functional Loss SNV dbSNP153 33..33 33 - - - 58333 RMVar_ID_58333 Human_SNP_ID_457497814 m1A Human chr11 + 17559932 17559932 17559932 GGGAGGAAGGAAGGAAAGAAGGAAGGGAGGGAAGGAAGGAAGGAAGGAGCAAACAATTAACAAAT GGGAGGAAGGAAGGAAAGAAGGAAGGGAGGGAGGGAAGGAAGGAAGGAGCAAACAATTAACAAAT A G OTOG Ensembl:ENSG00000188162 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17559919..17560030 26863196 MeRIP-seq:(Medium) rs77199445 Functional Loss SNV dbSNP153 33..33 33 - - - 58334 RMVar_ID_58334 Human_SNP_ID_457571122 m1A Human chr11 - 17856210 17856210 17856210 AGGGGAGCCAGCCATGGGCAGCAGAGATATTGACAGAGGGTAAAGGATGAGCTTGTTAGTTATAT AGGGGAGCCAGCCATGGGCAGCAGAGATATTGGCAGAGGGTAAAGGATGAGCTTGTTAGTTATAT T C SERGEF Ensembl:ENSG00000129158 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:17856197..17856266 26863196 MeRIP-seq:(Medium) rs1259032476 Functional Loss SNV dbSNP153 33..33 33 - - - 58335 RMVar_ID_58335 Human_SNP_ID_457599381 m1A Human chr11 - 17988755 17988755 17988755 CACCTCTTTTGTTACCCTTCTGTTTGTTTAAGATGCAGGAGAGGTGTATGTTTGGGGAAGCAACA CACCTCTTTTGTTACCCTTCTGTTTGTTTAAGGTGCAGGAGAGGTGTATGTTTGGGGAAGCAACA T C SERGEF Ensembl:ENSG00000129158 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17988720..17992992 32194978 MeRIP-seq:(Medium) rs1294933012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24363562 Human_Splice_Rec_1217782,Human_Splice_Rec_1217800,Human_Splice_Rec_1217822,Human_Splice_Rec_1217842,Human_Splice_Rec_1217860,Human_Splice_Rec_1217870,Human_Splice_Rec_1217902,Human_Splice_Rec_1217930,Human_Splice_Rec_1217948,Human_Splice_Rec_1217964 RMVar_hsa_circ_148530,RMVar_hsa_circ_119279,RMVar_hsa_circ_301534,RMVar_hsa_circ_148534,RMVar_hsa_circ_282248,RMVar_hsa_circ_148532,RMVar_hsa_circ_336029,RMVar_hsa_circ_148529,RMVar_hsa_circ_295612,RMVar_hsa_circ_317848,RMVar_hsa_circ_148531,RMVar_hsa_circ_300477,RMVar_hsa_circ_148536,RMVar_hsa_circ_277836,RMVar_hsa_circ_148535,RMVar_hsa_circ_148533 58336 RMVar_ID_58336 Human_SNP_ID_457604999 m1A Human chr11 - 18012795 18012784 18012795 AGGATCCTGGGCTGGGAGCGGAGGGGGAGCGGAGGAGGAGCGGGCGGGCGGGGAAGGAAGGGTCT AGGATCCTGGGCTGGGAGCGGAGGGGGAGCGG___________GCGGGCGGGGAAGGAAGGGTCT CCCGCTCCTCCT C SERGEF,AC055860.1 Ensembl:ENSG00000129158,Ensembl:ENSG00000255448 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:18012790..18012906 26863196 MeRIP-seq:(Medium) rs1321443709 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_5314106,Human_RBP_ID_8174159,Human_RBP_ID_18932302,Human_RBP_ID_21965232,Human_RBP_ID_22709075,Human_RBP_ID_24363567 58337 RMVar_ID_58337 Human_SNP_ID_457605015 m1A Human chr11 - 18012811 18012811 18012811 CCGGGCTCTGGGTTGAAGGATCCTGGGCTGGGAGCGGAGGGGGAGCGGAGGAGGAGCGGGCGGGC CCGGGCTCTGGGTTGAAGGATCCTGGGCTGGGGGCGGAGGGGGAGCGGAGGAGGAGCGGGCGGGC T C SERGEF,AC055860.1 Ensembl:ENSG00000129158,Ensembl:ENSG00000255448 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:18012789..18012909 26863196 MeRIP-seq:(Medium) rs1323576886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5314106,Human_RBP_ID_21965232 58338 RMVar_ID_58338 Human_SNP_ID_457626656 m1A Human chr11 - 18103328 18103328 18103328 TTGTGTTTCTGAAGATTGTTAGCCCTGAAAACACCAAATCTAGCTCAGATGATGAGGAGCAGCTG TTGTGTTTCTGAAGATTGTTAGCCCTGAAAACCCCAAATCTAGCTCAGATGATGAGGAGCAGCTG T G SAAL1 Ensembl:ENSG00000166788 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:18103278..18103419 26863196 MeRIP-seq:(Medium) rs761484261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362063,Human_RBP_ID_27803284 Human_Splice_Rec_1218074,Human_Splice_Rec_1218075,Human_Splice_Rec_1218094,Human_Splice_Rec_1218095,Human_Splice_Rec_1218138,Human_Splice_Rec_1218139,Human_Splice_Rec_1218162,Human_Splice_Rec_1218163,Human_Splice_Rec_1218170,Human_Splice_Rec_1218171,Human_Splice_Rec_1218194,Human_Splice_Rec_1218195,Human_Splice_Rec_1218206,Human_Splice_Rec_1218207,Human_Splice_Rec_1218222,Human_Splice_Rec_1218223 RMVar_hsa_circ_35791,RMVar_hsa_circ_96511,RMVar_hsa_circ_148543,RMVar_hsa_circ_119124,RMVar_hsa_circ_334249,RMVar_hsa_circ_148546,RMVar_hsa_circ_343413 58339 RMVar_ID_58339 Human_SNP_ID_457627286 m1A Human chr11 - 18105814 18105813 18105814 CTCTGGCGAATCCTCCTGCCCCGGGAGCCGCCATCCCCACAAAGACCCCTCCCCAGGCGTGCGCT CTCTGGCGAATCCTCCTGCCCCGGGAGCCGCC_TCCCCACAAAGACCCCTCCCCAGGCGTGCGCT AT A SAAL1 Ensembl:ENSG00000166788 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:18105812..18106053 26863196 MeRIP-seq:(Medium) rs1294081388 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_96511,RMVar_hsa_circ_148543,RMVar_hsa_circ_119124,RMVar_hsa_circ_148546 58340 RMVar_ID_58340 Human_SNP_ID_457627332 m1A Human chr11 + 18105911 18105911 18105911 ACCCCACGCGTGGCGCGAGTTTCCACACCTGGATGAGTCCGCTGAGGACGCCGAAGAGCCAGTGT ACCCCACGCGTGGCGCGAGTTTCCACACCTGGGTGAGTCCGCTGAGGACGCCGAAGAGCCAGTGT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:18105908..18106050 26863196 MeRIP-seq:(Medium) rs550001896 Functional Loss SNV dbSNP153 33..33 33 - - - 58341 RMVar_ID_58341 Human_SNP_ID_457627375 m1A Human chr11 - 18106001 18105999 18106002 CAACCCCTCGCCGCCGCCGCCGGGTCGCGACAAGGAGGAGGAGGAGGAGGTGGCCGGTGGAGACT CAACCCCTCGCCGCCGCCGCCGGGTCGCGAC___GAGGAGGAGGAGGAGGTGGCCGGTGGAGACT CCTT C SAAL1 Ensembl:ENSG00000166788 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:18105911..18106041 26863410 MeRIP-seq:(Medium) rs746292570 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4184698,Human_RBP_ID_23497630 Human_Splice_Rec_1218073,Human_Splice_Rec_1218093,Human_Splice_Rec_1218137,Human_Splice_Rec_1218161,Human_Splice_Rec_1218169,Human_Splice_Rec_1218193,Human_Splice_Rec_1218205,Human_Splice_Rec_1218221 RMVar_hsa_circ_96511,RMVar_hsa_circ_148543,RMVar_hsa_circ_119124,RMVar_hsa_circ_148546 58342 RMVar_ID_58342 Human_SNP_ID_457627377 m1A Human chr11 - 18106001 18106000 18106001 CAACCCCTCGCCGCCGCCGCCGGGTCGCGACAAGGAGGAGGAGGAGGAGGTGGCCGGTGGAGACT CAACCCCTCGCCGCCGCCGCCGGGTCGCGACA_GGAGGAGGAGGAGGAGGTGGCCGGTGGAGACT CT C SAAL1 Ensembl:ENSG00000166788 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:18105911..18106041 26863410 MeRIP-seq:(Medium) rs1554904717 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4184698,Human_RBP_ID_23497630 Human_Splice_Rec_1218073,Human_Splice_Rec_1218093,Human_Splice_Rec_1218137,Human_Splice_Rec_1218161,Human_Splice_Rec_1218169,Human_Splice_Rec_1218193,Human_Splice_Rec_1218205,Human_Splice_Rec_1218221 RMVar_hsa_circ_96511,RMVar_hsa_circ_148543,RMVar_hsa_circ_119124,RMVar_hsa_circ_148546 58343 RMVar_ID_58343 Human_SNP_ID_457627385 m1A Human chr11 + 18106009 18106009 18106009 CCGGCCACCTCCTCCTCCTCCTCCTTGTCGCGACCCGGCGGCGGCGGCGAGGGGTTGCGGTCCAT CCGGCCACCTCCTCCTCCTCCTCCTTGTCGCGTCCCGGCGGCGGCGGCGAGGGGTTGCGGTCCAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:18103276..18106075 26863196 MeRIP-seq:(Medium) rs1408137773 Functional Loss SNV dbSNP153 33..33 33 - - - 58344 RMVar_ID_58344 Human_SNP_ID_457678735 m1A Human chr11 - 18302207 18302205 18302208 ATTTATATGAGTAAGTATAGAAAAAGATGAGGAGAAAAAAATGAGTCCTCCAGACCAGAGGACTG ATTTATATGAGTAAGTATAGAAAAAGATGAG___AAAAAAATGAGTCCTCCAGACCAGAGGACTG TCTC T HPS5 Ensembl:ENSG00000110756 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:18302156..18302263 26863196 MeRIP-seq:(Medium) rs1246918614 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_77153,RMVar_hsa_circ_60097,RMVar_hsa_circ_33613,RMVar_hsa_circ_74742,RMVar_hsa_circ_148554,RMVar_hsa_circ_25172,RMVar_hsa_circ_148567,RMVar_hsa_circ_310657,RMVar_hsa_circ_374122,RMVar_hsa_circ_148566,RMVar_hsa_circ_148568,RMVar_hsa_circ_59509,RMVar_hsa_circ_65752,RMVar_hsa_circ_45685,RMVar_hsa_circ_304216,RMVar_hsa_circ_314203,RMVar_hsa_circ_54886,RMVar_hsa_circ_148570,RMVar_hsa_circ_68058,RMVar_hsa_circ_148573,RMVar_hsa_circ_76873,RMVar_hsa_circ_300729,RMVar_hsa_circ_311219,RMVar_hsa_circ_351864,RMVar_hsa_circ_104432,RMVar_hsa_circ_148575,RMVar_hsa_circ_72367,RMVar_hsa_circ_148574,RMVar_hsa_circ_148572 58345 RMVar_ID_58345 Human_SNP_ID_457683809 m1A Human chr11 + 18322040 18322040 18322040 TTCAAAGCCAGGCTCACAGACCAGCAGCCCGGAGGTCCCAGCCCAGCTCCACCACATCCAGGGCA TTCAAAGCCAGGCTCACAGACCAGCAGCCCGGGGGTCCCAGCCCAGCTCCACCACATCCAGGGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:18321991..18322074 26863196 MeRIP-seq:(Medium) rs981634115 Functional Loss SNV dbSNP153 33..33 33 - - - 58346 RMVar_ID_58346 Human_SNP_ID_457683819 m1A Human chr11 + 18322072 18322072 18322072 AGGTCCCAGCCCAGCTCCACCACATCCAGGGCAGTACCTCGCAGCTCTCAGTAGATCGGATCTTG AGGTCCCAGCCCAGCTCCACCACATCCAGGGCTGTACCTCGCAGCTCTCAGTAGATCGGATCTTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:18322021..18322107 26863196 MeRIP-seq:(Medium) rs1228458349 Functional Loss SNV dbSNP153 33..33 33 - - - 58347 RMVar_ID_58347 Human_SNP_ID_457683986 m1A Human chr11 + 18322372 18322372 18322372 CCGTTGCGGGCTGGAGACACGGCGCCGACTGGAACCGGAGGAGCTCTAGGCCAAATGGTTGGGCC CCGTTGCGGGCTGGAGACACGGCGCCGACTGGTACCGGAGGAGCTCTAGGCCAAATGGTTGGGCC A T GTF2H1 Ensembl:ENSG00000110768 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:18322322..18322499 26863196 MeRIP-seq:(Medium) rs962097517 Functional Loss SNV dbSNP153 33..33 33 - - - 58348 RMVar_ID_58348 Human_SNP_ID_457703890 m1A Human chr11 + 18394616 18394616 18394616 ATTCCGGATCTCATTGCCACGCGCCCCCGACGACCGCCCGACGTGCATTCCCGGTACGGTAGGGC ATTCCGGATCTCATTGCCACGCGCCCCCGACGGCCGCCCGACGTGCATTCCCGGTACGGTAGGGC A G LDHA Ensembl:ENSG00000134333 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:18394525..18394698;chr11:18394551..18394750;chr11:18394551..18394753;chr11:18394551..18394749;chr11:18394471..18394736;chr11:18394456..18394713;chr11:18394489..18394706 26863196 MeRIP-seq:(Medium) rs764991833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226535,Human_RBP_ID_393406,Human_RBP_ID_871343,Human_RBP_ID_1777602,Human_RBP_ID_4184702,Human_RBP_ID_6061270,Human_RBP_ID_8348246,Human_RBP_ID_9321339,Human_RBP_ID_11580883,Human_RBP_ID_17350066,Human_RBP_ID_18605923,Human_RBP_ID_19049145,Human_RBP_ID_22034331,Human_RBP_ID_22432821,Human_RBP_ID_22532344 Human_Splice_Rec_1218719,Human_Splice_Rec_1218727,Human_Splice_Rec_1218729,Human_Splice_Rec_1218737,Human_Splice_Rec_1218749,Human_Splice_Rec_1218761,Human_Splice_Rec_1218767,Human_Splice_Rec_1218771,Human_Splice_Rec_1218779,Human_Splice_Rec_1218787,Human_Splice_Rec_1218793,Human_Splice_Rec_1218803,Human_Splice_Rec_1218815,Human_Splice_Rec_1218829 RMVar_hsa_circ_148590,RMVar_hsa_circ_91084,RMVar_hsa_circ_94174,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592 58349 RMVar_ID_58349 Human_SNP_ID_457703898 m1A Human chr11 - 18394632 18394632 18394632 GCGCCGTGCGCGCAGGGCCCTACCGTACCGGGAATGCACGTCGGGCGGTCGTCGGGGGCGCGTGG GCGCCGTGCGCGCAGGGCCCTACCGTACCGGGGATGCACGTCGGGCGGTCGTCGGGGGCGCGTGG T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:18394551..18394704 26863410 MeRIP-seq:(Medium) rs1407531219 Functional Loss SNV dbSNP153 33..33 33 - - - 58350 RMVar_ID_58350 Human_SNP_ID_457704593 m1A Human chr11 + 18396881 18396881 18396881 ACTCTAAAGGATCAGCTGATTTATAATCTTCTAAAGGAAGAACAGACCCCCCAGAATAAGATTAC ACTCTAAAGGATCAGCTGATTTATAATCTTCTCAAGGAAGAACAGACCCCCCAGAATAAGATTAC A C LDHA Ensembl:ENSG00000134333 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:18396760..18396925 26863196 MeRIP-seq:(Medium) rs371221146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393409,Human_RBP_ID_749553,Human_RBP_ID_1455590,Human_RBP_ID_1777604,Human_RBP_ID_3372320,Human_RBP_ID_22434243,Human_RBP_ID_26888666,Human_RBP_ID_27616476 Human_Splice_Rec_1218720,Human_Splice_Rec_1218721,Human_Splice_Rec_1218728,Human_Splice_Rec_1218730,Human_Splice_Rec_1218731,Human_Splice_Rec_1218738,Human_Splice_Rec_1218739,Human_Splice_Rec_1218750,Human_Splice_Rec_1218751,Human_Splice_Rec_1218764,Human_Splice_Rec_1218765,Human_Splice_Rec_1218768,Human_Splice_Rec_1218769,Human_Splice_Rec_1218772,Human_Splice_Rec_1218773,Human_Splice_Rec_1218780,Human_Splice_Rec_1218781,Human_Splice_Rec_1218788,Human_Splice_Rec_1218789,Human_Splice_Rec_1218794,Human_Splice_Rec_1218795,Human_Splice_Rec_1218804,Human_Splice_Rec_1218805,Human_Splice_Rec_1218816,Human_Splice_Rec_1218817,Human_Splice_Rec_1218830,Human_Splice_Rec_1218831,Human_Splice_Rec_1218842,Human_Splice_Rec_1218843,Human_Splice_Rec_1218850,Human_Splice_Rec_1218851,Human_Splice_Rec_1218856,Human_Splice_Rec_1218857,Human_Splice_Rec_1218870,Human_Splice_Rec_1218871,Human_Splice_Rec_1218883,Human_Splice_Rec_1218895,Human_Splice_Rec_1218903 RMVar_hsa_circ_91084,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592,RMVar_hsa_circ_148593,RMVar_hsa_circ_108242 58351 RMVar_ID_58351 Human_SNP_ID_457706441 m1A Human chr11 + 18402940 18402940 18402940 TGCAATCTGGATTCAGCCCGATTCCGTTACCTAATGGGGGAAAGGCTGGGAGTTCACCCATTAAG TGCAATCTGGATTCAGCCCGATTCCGTTACCTGATGGGGGAAAGGCTGGGAGTTCACCCATTAAG A G LDHA Ensembl:ENSG00000134333 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4820 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - Human_RBP_ID_393417,Human_RBP_ID_4156073,Human_RBP_ID_8348261,Human_RBP_ID_9001787,Human_RBP_ID_17231652,Human_RBP_ID_23497776 Human_Splice_Rec_1218743,Human_Splice_Rec_1218757,Human_Splice_Rec_1218785,Human_Splice_Rec_1218791,Human_Splice_Rec_1218809,Human_Splice_Rec_1218823,Human_Splice_Rec_1218837,Human_Splice_Rec_1218863,Human_Splice_Rec_1218877,Human_Splice_Rec_1218889,Human_Splice_Rec_1218899,Human_Splice_Rec_1218909,Human_Splice_Rec_1218919,Human_Splice_Rec_1218923,Human_Splice_Rec_1218929 Human_miRNA_ID_2970526 Clinvar_Rec_176 RMVar_hsa_circ_37723,RMVar_hsa_circ_338133,RMVar_hsa_circ_148595,RMVar_hsa_circ_106856,RMVar_hsa_circ_270675,RMVar_hsa_circ_304781,RMVar_hsa_circ_108291,RMVar_hsa_circ_148596,RMVar_hsa_circ_96667,RMVar_hsa_circ_148594,RMVar_hsa_circ_299052,RMVar_hsa_circ_148597,RMVar_hsa_circ_148598 58352 RMVar_ID_58352 Human_SNP_ID_457706442 m1A Human chr11 + 18402940 18402940 18402940 TGCAATCTGGATTCAGCCCGATTCCGTTACCTAATGGGGGAAAGGCTGGGAGTTCACCCATTAAG TGCAATCTGGATTCAGCCCGATTCCGTTACCTTATGGGGGAAAGGCTGGGAGTTCACCCATTAAG A T LDHA Ensembl:ENSG00000134333 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393417,Human_RBP_ID_4156073,Human_RBP_ID_8348261,Human_RBP_ID_9001787,Human_RBP_ID_17231652,Human_RBP_ID_23497776 Human_Splice_Rec_1218743,Human_Splice_Rec_1218757,Human_Splice_Rec_1218785,Human_Splice_Rec_1218791,Human_Splice_Rec_1218809,Human_Splice_Rec_1218823,Human_Splice_Rec_1218837,Human_Splice_Rec_1218863,Human_Splice_Rec_1218877,Human_Splice_Rec_1218889,Human_Splice_Rec_1218899,Human_Splice_Rec_1218909,Human_Splice_Rec_1218919,Human_Splice_Rec_1218923,Human_Splice_Rec_1218929 Human_miRNA_ID_2970526 Clinvar_Rec_176 RMVar_hsa_circ_37723,RMVar_hsa_circ_338133,RMVar_hsa_circ_148595,RMVar_hsa_circ_106856,RMVar_hsa_circ_270675,RMVar_hsa_circ_304781,RMVar_hsa_circ_108291,RMVar_hsa_circ_148596,RMVar_hsa_circ_96667,RMVar_hsa_circ_148594,RMVar_hsa_circ_299052,RMVar_hsa_circ_148597,RMVar_hsa_circ_148598 58353 RMVar_ID_58353 Human_SNP_ID_457707723 m1A Human chr11 + 18407536 18407536 18407536 TTAGTGTGAAATAGTTCTGCCACCTCTGACGCACCACTGCCAATGCTGTACGTACTGCATTTGCC TTAGTGTGAAATAGTTCTGCCACCTCTGACGCGCCACTGCCAATGCTGTACGTACTGCATTTGCC A G LDHA Ensembl:ENSG00000134333 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:18407485..18407561 26863196 MeRIP-seq:(Medium) rs200774396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226537,Human_RBP_ID_393438,Human_RBP_ID_749570,Human_RBP_ID_807828,Human_RBP_ID_869992,Human_RBP_ID_1455606,Human_RBP_ID_1777625,Human_RBP_ID_2262540,Human_RBP_ID_3372329,Human_RBP_ID_6061298,Human_RBP_ID_8348283,Human_RBP_ID_9001797,Human_RBP_ID_11581075,Human_RBP_ID_17231665,Human_RBP_ID_17348106,Human_RBP_ID_17464127,Human_RBP_ID_17793402,Human_RBP_ID_18249346,Human_RBP_ID_18605936,Human_RBP_ID_21883363,Human_RBP_ID_23206856,Human_RBP_ID_23497792,Human_RBP_ID_26410406,Human_RBP_ID_27154064,Human_RBP_ID_27410610 Human_miRNA_ID_282901,Human_miRNA_ID_2457401,Human_miRNA_ID_2462321,Human_miRNA_ID_2634964,Human_miRNA_ID_2637651 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 58354 RMVar_ID_58354 Human_SNP_ID_457707805 m1A Human chr11 + 18407777 18407777 18407777 AGTGTACATTACCATATAATGTAAAAAGATCTACATACAAACAATGCAACCAACTATCCAAGTGT AGTGTACATTACCATATAATGTAAAAAGATCTGCATACAAACAATGCAACCAACTATCCAAGTGT A G LDHA Ensembl:ENSG00000134333 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:18407726..18407825 32194978 MeRIP-seq:(Medium) rs1457181879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393447,Human_RBP_ID_1455608,Human_RBP_ID_1777631,Human_RBP_ID_3372332,Human_RBP_ID_11581085,Human_RBP_ID_17231670,Human_RBP_ID_17348112,Human_RBP_ID_17464135,Human_RBP_ID_17793406,Human_RBP_ID_18249351,Human_RBP_ID_21883369,Human_RBP_ID_23497801,Human_RBP_ID_26402873,Human_RBP_ID_27200218,Human_RBP_ID_27616493 Human_miRNA_ID_2445504,Human_miRNA_ID_2446890 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 58355 RMVar_ID_58355 Human_SNP_ID_457739071 m1A Human chr11 - 18526867 18526867 18526867 GTGCGATTGTGTGGGACGGTCTGGGGCAGCCCAGCAGCGGCTGACCCTCTGCCTGCGGGGAAGGG GTGCGATTGTGTGGGACGGTCTGGGGCAGCCCGGCAGCGGCTGACCCTCTGCCTGCGGGGAAGGG T C TSG101 Ensembl:ENSG00000074319 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:18526774..18526916 26863196 MeRIP-seq:(Medium) rs745447761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226246,Human_RBP_ID_871534,Human_RBP_ID_4183965,Human_RBP_ID_5138514,Human_RBP_ID_5436265,Human_RBP_ID_9321340,Human_RBP_ID_9352630,Human_RBP_ID_17649036,Human_RBP_ID_18416526,Human_RBP_ID_22432842,Human_RBP_ID_23206860,Human_RBP_ID_23497861,Human_RBP_ID_27410623 Human_Splice_Rec_1219077,Human_Splice_Rec_1219105,Human_Splice_Rec_1219125,Human_Splice_Rec_1219151,Human_Splice_Rec_1219157,Human_Splice_Rec_1219167,Human_Splice_Rec_1219173 RMVar_hsa_circ_91752,RMVar_hsa_circ_148606 58356 RMVar_ID_58356 Human_SNP_ID_457739075 m1A Human chr11 - 18526872 18526872 18526872 GGGGTGTGCGATTGTGTGGGACGGTCTGGGGCAGCCCAGCAGCGGCTGACCCTCTGCCTGCGGGG GGGGTGTGCGATTGTGTGGGACGGTCTGGGGCGGCCCAGCAGCGGCTGACCCTCTGCCTGCGGGG T C TSG101 Ensembl:ENSG00000074319 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:18525661..18526925;chr11:18525661..18526950;chr11:18526760..18526925 26863196 MeRIP-seq:(Medium) rs1370582151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226246,Human_RBP_ID_4183965,Human_RBP_ID_5138514,Human_RBP_ID_5436265,Human_RBP_ID_9321340,Human_RBP_ID_9352630,Human_RBP_ID_17649036,Human_RBP_ID_18416526,Human_RBP_ID_22432842,Human_RBP_ID_23206860,Human_RBP_ID_23497861,Human_RBP_ID_27410623 Human_Splice_Rec_1219077,Human_Splice_Rec_1219105,Human_Splice_Rec_1219125,Human_Splice_Rec_1219151,Human_Splice_Rec_1219157,Human_Splice_Rec_1219167,Human_Splice_Rec_1219173 RMVar_hsa_circ_91752,RMVar_hsa_circ_148606 58357 RMVar_ID_58357 Human_SNP_ID_457739079 m1A Human chr11 + 18526878 18526878 18526878 AGGCAGAGGGTCAGCCGCTGCTGGGCTGCCCCAGACCGTCCCACACAATCGCACACCCCCAACCC AGGCAGAGGGTCAGCCGCTGCTGGGCTGCCCCGGACCGTCCCACACAATCGCACACCCCCAACCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:18519551..18526925 26863196 MeRIP-seq:(Medium) rs1222927069 Functional Loss SNV dbSNP153 33..33 33 - - - 58358 RMVar_ID_58358 Human_SNP_ID_457754622 m1A Human chr11 + 18589880 18589880 18589880 TGAGGGAGTAAGTGTTACGAATCCGAGTGCAGACAAAGCAGTAGCCTAAGGCATGTGCCCAGGGA TGAGGGAGTAAGTGTTACGAATCCGAGTGCAGTCAAAGCAGTAGCCTAAGGCATGTGCCCAGGGA A T SPTY2D1OS Ensembl:ENSG00000247595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:18589829..18590054 26863196 MeRIP-seq:(Medium) rs920948878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18605965 58359 RMVar_ID_58359 Human_SNP_ID_457765888 m1A Human chr11 + 18634368 18634368 18634368 GCCAACTGCACTGCCTCGGGAGCCCCACTCCCACCCCGCCTCTGCGGGACCACTTCCGGCGCCTT GCCAACTGCACTGCCTCGGGAGCCCCACTCCCCCCCCGCCTCTGCGGGACCACTTCCGGCGCCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:18634318..18634460 26863196 MeRIP-seq:(Medium) rs975977724 Functional Loss SNV dbSNP153 33..33 33 - - - 58360 RMVar_ID_58360 Human_SNP_ID_457773777 m1A Human chr11 + 18665325 18665325 18665325 ACTGTCCAATGGTGAAAAAAGAAGTAGAAATCATGGCCCACCTCCCTCCTGGGGTCGTCGCCCTC ACTGTCCAATGGTGAAAAAAGAAGTAGAAATCGTGGCCCACCTCCCTCCTGGGGTCGTCGCCCTC A G SRSF3P1 Ensembl:ENSG00000257043 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878929748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18432562 58361 RMVar_ID_58361 Human_SNP_ID_457889186 m1A Human chr11 + 19117218 19117218 19117218 GCTGGCGGGCTGGCGGCAGTCGCTACTTGCCTAGTAGCCTCAGCCGCTGTGGGCTCCTGGGGAGA GCTGGCGGGCTGGCGGCAGTCGCTACTTGCCTGGTAGCCTCAGCCGCTGTGGGCTCCTGGGGAGA A G ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:19117169..19117335 26863196 MeRIP-seq:(Medium) rs947755731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227178,Human_RBP_ID_750548,Human_RBP_ID_4156232,Human_RBP_ID_18416793 Human_Splice_Rec_1219707,Human_Splice_Rec_1219735,Human_Splice_Rec_1219761,Human_Splice_Rec_1219791 RMVar_hsa_circ_148637,RMVar_hsa_circ_102157 58362 RMVar_ID_58362 Human_SNP_ID_457889358 m1A Human chr11 + 19117844 19117844 19117844 GGAGAGGGGAGGTACACCACAGCGATCTGCAGAATCTCAAAGGACAATATTCCGTGGAGGAGGTG GGAGAGGGGAGGTACACCACAGCGATCTGCAGGATCTCAAAGGACAATATTCCGTGGAGGAGGTG A G ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:19117841..19117912 26863196 MeRIP-seq:(Medium) rs983749713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344943,Human_RBP_ID_11582027 Human_Splice_Rec_1219793 RMVar_hsa_circ_148637,RMVar_hsa_circ_102157 58363 RMVar_ID_58363 Human_SNP_ID_458007738 m1A Human chr11 + 19598202 19598202 19598202 CGTCTCTTCTGCAAGGGCAGTGCCCCAGCCTCAGCCACACTTCTGATCTGCAGTCCAACAGACCT CGTCTCTTCTGCAAGGGCAGTGCCCCAGCCTCCGCCACACTTCTGATCTGCAGTCCAACAGACCT A C NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:19598152..19598296 26863196 MeRIP-seq:(Medium) rs1055581839 Functional Loss SNV dbSNP153 33..33 33 - - - 58364 RMVar_ID_58364 Human_SNP_ID_458036719 m1A Human chr11 - 19713182 19713182 19713182 GGAAGGAAAGGAGACAGCAGCGAAGGAAGGAGAGAAGAAGGGCGCAAGGGTCCCAAGACGTCTCC GGAAGGAAAGGAGACAGCAGCGAAGGAAGGAGTGAAGAAGGGCGCAAGGGTCCCAAGACGTCTCC T A LOC100126784 RNACentral:URS000075CF88 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:19713080..19713224 32194978 MeRIP-seq:(Medium) rs1426290624 Functional Loss SNV dbSNP153 33..33 33 - - - 58365 RMVar_ID_58365 Human_SNP_ID_458037421 m1A Human chr11 - 19715450 19715450 19715450 CACCGACTGCCCACTACACCTCATAAACCCCAAGTCCATGGATGAAGGGAAACCCCATGCAGAAG CACCGACTGCCCACTACACCTCATAAACCCCACGTCCATGGATGAAGGGAAACCCCATGCAGAAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19715439..19715550 26863196 MeRIP-seq:(Medium) rs1319701 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6826,GWAS_ID_6827,GWAS_ID_6828,GWAS_ID_6829,GWAS_ID_6830,GWAS_ID_6831,GWAS_ID_6832 58366 RMVar_ID_58366 Human_SNP_ID_458040561 m1A Human chr11 - 19729216 19729216 19729216 CATCTTCTAGGATCCCATTCCTGCTTGCTCCAAGTCACCCAGTTCCCTCCTTCCCTCAGTCTTCC CATCTTCTAGGATCCCATTCCTGCTTGCTCCAGGTCACCCAGTTCCCTCCTTCCCTCAGTCTTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19729203..19729292 26863196 MeRIP-seq:(Medium) rs1368928164 Functional Loss SNV dbSNP153 33..33 33 - - - 58367 RMVar_ID_58367 Human_SNP_ID_458051525 m1A Human chr11 - 19776561 19776561 19776561 ACACACACACACACACCCCTGCCCCAGCCCACACGCTGCGTTCCCAGCAATATTTATTTCCTGCC ACACACACACACACACCCCTGCCCCAGCCCACCCGCTGCGTTCCCAGCAATATTTATTTCCTGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19776550..19776690 26863196 MeRIP-seq:(Medium) rs996618852 Functional Loss SNV dbSNP153 33..33 33 - - - 58368 RMVar_ID_58368 Human_SNP_ID_458051708 m1A Human chr11 + 19776782 19776782 19776782 TGTCAACTTGCGTGAGTTCTGTGCAGAAAGAAAATGCGGATGGAGATGAGTGCGCATAGTGAGGC TGTCAACTTGCGTGAGTTCTGTGCAGAAAGAAGATGCGGATGGAGATGAGTGCGCATAGTGAGGC A G NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19776771..19776911 26863196 MeRIP-seq:(Medium) rs910215086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23498510 RMVar_hsa_circ_107272,RMVar_hsa_circ_148647 58369 RMVar_ID_58369 Human_SNP_ID_458076861 m1A Human chr11 + 19880058 19880058 19880058 CACCCCTCAGCAGCAGGTGCCAGTCACTCCCCAAGCCCCGTGCCAGCCTCACCAGCCAGCGCCAC CACCCCTCAGCAGCAGGTGCCAGTCACTCCCCCAGCCCCGTGCCAGCCTCACCAGCCAGCGCCAC A C NAV2 Ensembl:ENSG00000166833 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:19879946..19880100 26863196 MeRIP-seq:(Medium) rs770962584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1219975,Human_Splice_Rec_1220049,Human_Splice_Rec_1220125,Human_Splice_Rec_1220197,Human_Splice_Rec_1220273,Human_Splice_Rec_1220347 Human_miRNA_ID_2051689,Human_miRNA_ID_2367197,Human_miRNA_ID_2714628,Human_miRNA_ID_3014995,Human_miRNA_ID_3050612 RMVar_hsa_circ_148652,RMVar_hsa_circ_107272,RMVar_hsa_circ_293325,RMVar_hsa_circ_148647,RMVar_hsa_circ_337242,RMVar_hsa_circ_372438,RMVar_hsa_circ_318062,RMVar_hsa_circ_36342,RMVar_hsa_circ_82910,RMVar_hsa_circ_148654,RMVar_hsa_circ_13725,RMVar_hsa_circ_148653,RMVar_hsa_circ_619,RMVar_hsa_circ_148651,RMVar_hsa_circ_148655,RMVar_hsa_circ_331479,RMVar_hsa_circ_330571,RMVar_hsa_circ_324562,RMVar_hsa_circ_347726,RMVar_hsa_circ_34858,RMVar_hsa_circ_148656,RMVar_hsa_circ_290060,RMVar_hsa_circ_148657 58370 RMVar_ID_58370 Human_SNP_ID_458084440 m1A Human chr11 - 19910306 19910306 19910306 TTGCACCTCCAGCAATTTGTACAGCATTTAACATAAAAGAGGGGCTCAATGATTAGTGAATTTAG TTGCACCTCCAGCAATTTGTACAGCATTTAACGTAAAAGAGGGGCTCAATGATTAGTGAATTTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19910300..19910465 26863196 MeRIP-seq:(Medium) rs2625335 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6833 58371 RMVar_ID_58371 Human_SNP_ID_212156939 m1A Human chr4 - 165112813 165112813 165112813 TCGCGGCCAGAGGCTTACAGGTCCAGGTGGAGAGGCCGGGCTGGCCAGGGCTTCGGCCTCCGGCG TCGCGGCCAGAGGCTTACAGGTCCAGGTGGAGGGGCCGGGCTGGCCAGGGCTTCGGCCTCCGGCG T C TMEM192 Ensembl:ENSG00000170088 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:165112688..165112836 26863196 MeRIP-seq:(Medium) rs749650821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794745,Human_RBP_ID_18424645 Human_Splice_Rec_620245,Human_Splice_Rec_620267 58372 RMVar_ID_58372 Human_SNP_ID_212179494 m1A Human chr4 + 165207749 165207749 165207749 GCCGCCGCCGCAGGTGGTGGCGCGCGGTGAGGAGAGCGCGGCGCCCCCTCCGGGGCGGATGGAAC GCCGCCGCCGCAGGTGGTGGCGCGCGGTGAGGTGAGCGCGGCGCCCCCTCCGGGGCGGATGGAAC A T KLHL2 Ensembl:ENSG00000109466 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:165207614..165207868 26863196 MeRIP-seq:(Medium) rs1190263418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_615996,Human_RBP_ID_4795692 58373 RMVar_ID_58373 Human_SNP_ID_212210496 m1A Human chr4 + 165342967 165342967 165342967 AGCTTTATTTCTATTTACCCTTCCATTTTTGTATATCAAATTTCCATTGTCATTAAAAACTGTAT AGCTTTATTTCTATTTACCCTTCCATTTTTGTGTATCAAATTTCCATTGTCATTAAAAACTGTAT A G MSMO1 Ensembl:ENSG00000052802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1641675,Human_RBP_ID_5475293,Human_RBP_ID_7285229,Human_RBP_ID_8212761,Human_RBP_ID_8950290,Human_RBP_ID_15237758,Human_RBP_ID_17296111,Human_RBP_ID_18345328,Human_RBP_ID_24431347,Human_RBP_ID_24500621,Human_RBP_ID_26518190,Human_RBP_ID_26691061 Human_miRNA_ID_756040,Human_miRNA_ID_1178568,Human_miRNA_ID_1632164,Human_miRNA_ID_1672663 RMVar_hsa_circ_100844,RMVar_hsa_circ_229435,RMVar_hsa_circ_110729,RMVar_hsa_circ_229437 58374 RMVar_ID_58374 Human_SNP_ID_212210497 m1A Human chr4 + 165342967 165342967 165342967 AGCTTTATTTCTATTTACCCTTCCATTTTTGTATATCAAATTTCCATTGTCATTAAAAACTGTAT AGCTTTATTTCTATTTACCCTTCCATTTTTGTTTATCAAATTTCCATTGTCATTAAAAACTGTAT A T MSMO1 Ensembl:ENSG00000052802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1641675,Human_RBP_ID_5475293,Human_RBP_ID_7285229,Human_RBP_ID_8212761,Human_RBP_ID_8950290,Human_RBP_ID_15237758,Human_RBP_ID_17296111,Human_RBP_ID_18345328,Human_RBP_ID_24431347,Human_RBP_ID_24500621,Human_RBP_ID_26518190,Human_RBP_ID_26691061 Human_miRNA_ID_756040,Human_miRNA_ID_1178568,Human_miRNA_ID_1632164,Human_miRNA_ID_1672663 RMVar_hsa_circ_100844,RMVar_hsa_circ_229435,RMVar_hsa_circ_110729,RMVar_hsa_circ_229437 58375 RMVar_ID_58375 Human_SNP_ID_212343576 m1A Human chr4 + 165887258 165887258 165887258 AAGAGTGAGCTGGTGTAGTTGGTGGAAGAAGTAATGAGAAAGTGGGAGGAGGGAGGCTTGTTAGG AAGAGTGAGCTGGTGTAGTTGGTGGAAGAAGTCATGAGAAAGTGGGAGGAGGGAGGCTTGTTAGG A C TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:165887250..165887390 26863196 MeRIP-seq:(Medium) rs1274943948 Functional Loss SNV dbSNP153 33..33 33 - - - 58376 RMVar_ID_58376 Human_SNP_ID_212405846 m1A Human chr4 - 166142619 166142619 166142619 TCACATGGGACCCAGTTCCTCTTCAGCCTTCAAAGTTCTCATTTGAATATTGGCTACTGCCACCA TCACATGGGACCCAGTTCCTCTTCAGCCTTCAGAGTTCTCATTTGAATATTGGCTACTGCCACCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:166142559..166142630 26863196 MeRIP-seq:(Medium) rs1486935727 Functional Loss SNV dbSNP153 33..33 33 - - - 58377 RMVar_ID_58377 Human_SNP_ID_212419692 m1A Human chr4 - 166198371 166198371 166198371 ACAATTTGAAATAATGAGTAAGACAGGGTATTATTGGGTGAAAAGGAAGAGAAGGAGAAAACAGA ACAATTTGAAATAATGAGTAAGACAGGGTATTCTTGGGTGAAAAGGAAGAGAAGGAGAAAACAGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:166198333..166198420 26863196 MeRIP-seq:(Medium) rs1006450605 Functional Loss SNV dbSNP153 33..33 33 - - - 58378 RMVar_ID_58378 Human_SNP_ID_212432812 m1A Human chr4 + 166248718 166248717 166248718 TGAAAACAGGATTTGTAATTGTTGGAATGTGGAAGAGTGAAGGAAGGCTGACAGATATATGGATT TGAAAACAGGATTTGTAATTGTTGGAATGTGG_AGAGTGAAGGAAGGCTGACAGATATATGGATT GA G lnc-TLL1-4,lnc-TLL1-4:2,lnc-TLL1-4:3,lnc-TLL1-4:4 RNACentral:URS0000D5989A,RNACentral:URS0000D59962,RNACentral:URS0000D5CACA,RNACentral:URS0000D58039 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:166248677..166248744 26863196 MeRIP-seq:(Medium) rs1398031520 Functional Loss DEL dbSNP153 33..33 33 - - - 58379 RMVar_ID_58379 Human_SNP_ID_212964956 m1A Human chr4 - 168318461 168318461 168318461 GGGAACCTCCTGGGATCGCAAGGCCGTGGCGCACGGGCCCCCTGCTGGCCCGGAAGGCCGGGCGT GGGAACCTCCTGGGATCGCAAGGCCGTGGCGCCCGGGCCCCCTGCTGGCCCGGAAGGCCGGGCGT T G DDX60 Ensembl:ENSG00000137628 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:168318414..168318615 26863196 MeRIP-seq:(Medium) rs947547395 Functional Loss SNV dbSNP153 33..33 33 - - - 58380 RMVar_ID_58380 Human_SNP_ID_213004770 m1A Human chr4 + 168480234 168480234 168480234 CGAAGCTGCCGCCCGAGCCCAGTGGGCGCCCCAGCTTCCCTCGCCCGGCGCGCACGAAGCCACCA CGAAGCTGCCGCCCGAGCCCAGTGGGCGCCCCGGCTTCCCTCGCCCGGCGCGCACGAAGCCACCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168480097..168480475 26863196 MeRIP-seq:(Medium) rs953887148 Functional Loss SNV dbSNP153 33..33 33 - - - 58381 RMVar_ID_58381 Human_SNP_ID_213040498 m1A Human chr4 + 168631617 168631617 168631617 GCGCACACGCGCCCCTCGGCGAGACGCGGCGCATTCGCGCGCTGGAGACCGGCGGCCTCTCACCG GCGCACACGCGCCCCTCGGCGAGACGCGGCGCGTTCGCGCGCTGGAGACCGGCGGCCTCTCACCG A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:168631512..168631653 26863196 MeRIP-seq:(Medium) rs1041835184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99022,RMVar_hsa_circ_229474 58382 RMVar_ID_58382 Human_SNP_ID_213051903 m1A Human chr4 - 168679377 168679377 168679377 CACACCCCACAGCACACCACACACACACACACACCCACACACATCCATACTCACCCCACCACACA CACACCCCACAGCACACCACACACACACACACCCCCACACACATCCATACTCACCCCACCACACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:168679355..168679516 26863196 MeRIP-seq:(Medium) rs1331851116 Functional Loss SNV dbSNP153 33..33 33 - - - 58383 RMVar_ID_58383 Human_SNP_ID_213070215 m1A Human chr4 - 168755328 168755328 168755328 TTGCTCTTTCTATATAATTCAAGTCCCTGCCCATATTTTACTCCCCTGATCCTCCATCTAAATTA TTGCTCTTTCTATATAATTCAAGTCCCTGCCCGTATTTTACTCCCCTGATCCTCCATCTAAATTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:168755314..168755535 26863196 MeRIP-seq:(Medium) rs1034518703 Functional Loss SNV dbSNP153 33..33 33 - - - 58384 RMVar_ID_58384 Human_SNP_ID_213070530 m1A Human chr4 + 168756556 168756556 168756556 TTTGCTGATGGCTAGCACTCAGGATGTAAGGGAAAGAGAAGGATTGAGGCTAACTATTGAGTTTT TTTGCTGATGGCTAGCACTCAGGATGTAAGGGTAAGAGAAGGATTGAGGCTAACTATTGAGTTTT A T PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168756542..168756660 26863196 MeRIP-seq:(Medium) rs542955535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58385 RMVar_ID_58385 Human_SNP_ID_213070535 m1A Human chr4 - 168756580 168756580 168756580 CACCTTTCATGCAGTTCTTAGACCAAAACTCAATAGTTAGCCTCAATCCTTCTCTTTCCCTTACA CACCTTTCATGCAGTTCTTAGACCAAAACTCAGTAGTTAGCCTCAATCCTTCTCTTTCCCTTACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:168756565..168756655 26863196 MeRIP-seq:(Medium) rs1251864957 Functional Loss SNV dbSNP153 33..33 33 - - - 58386 RMVar_ID_58386 Human_SNP_ID_213077399 m1A Human chr4 + 168784330 168784330 168784330 ACTTCAGCCTGGGAAACAGAGCAAGACCCTGAAAAAAAAAAGAGAGAGAGAGAGAAAGAAAAGAA ACTTCAGCCTGGGAAACAGAGCAAGACCCTGAGAAAAAAAAGAGAGAGAGAGAGAAAGAAAAGAA A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168784317..168784578 26863196 MeRIP-seq:(Medium) rs77326149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58387 RMVar_ID_58387 Human_SNP_ID_213089070 m1A Human chr4 - 168832114 168832114 168832114 TGCTGCCCGATTCCGCGTCCGGAGCGAGCGGGAGCTGCAGCGGGCTCCGCGGACCGGGCGCGGGG TGCTGCCCGATTCCGCGTCCGGAGCGAGCGGGCGCTGCAGCGGGCTCCGCGGACCGGGCGCGGGG T G AC080188.1 Ensembl:ENSG00000249609 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:168832092..168832224 26863196 MeRIP-seq:(Medium) rs1028507801 Functional Loss SNV dbSNP153 33..33 33 - - - 58388 RMVar_ID_58388 Human_SNP_ID_213089093 m1A Human chr4 + 168832163 168832163 168832163 GCGGAATCGGGCAGCAGCGGGAGGCGGCCCGGAGAGCCGAGGTAGGCGCGGGGAATCGGCCCTGA GCGGAATCGGGCAGCAGCGGGAGGCGGCCCGGGGAGCCGAGGTAGGCGCGGGGAATCGGCCCTGA A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168832140..168832255 26863196 MeRIP-seq:(Medium) rs1384245001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_621799,Human_Splice_Rec_621809 RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58389 RMVar_ID_58389 Human_SNP_ID_213097266 m1A Human chr4 + 168869810 168869795 168869810 ATAGTGGAATTCAGGACTGAGGGCTGGGTTAGAGAGATCAGGGAGTGAGAGTGATGCAGCTGACT ATAGTGGAATTCAGGACT_______________GAGATCAGGGAGTGAGAGTGATGCAGCTGACT TGAGGGCTGGGTTAGA T PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168869808..168869978 26863196 MeRIP-seq:(Medium) rs533676641 Functional Loss DEL dbSNP153 19..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58390 RMVar_ID_58390 Human_SNP_ID_213097270 m1A Human chr4 + 168869810 168869807 168869811 ATAGTGGAATTCAGGACTGAGGGCTGGGTTAGAGAGATCAGGGAGTGAGAGTGATGCAGCTGACT ATAGTGGAATTCAGGACTGAGGGCTGGGTT____AGATCAGGGAGTGAGAGTGATGCAGCTGACT TAGAG T PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168869808..168869978 26863196 MeRIP-seq:(Medium) rs150697690 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58391 RMVar_ID_58391 Human_SNP_ID_213097273 m1A Human chr4 + 168869810 168869810 168869810 ATAGTGGAATTCAGGACTGAGGGCTGGGTTAGAGAGATCAGGGAGTGAGAGTGATGCAGCTGACT ATAGTGGAATTCAGGACTGAGGGCTGGGTTAGCGAGATCAGGGAGTGAGAGTGATGCAGCTGACT A C PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:168869808..168869978 26863196 MeRIP-seq:(Medium) rs907809263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58392 RMVar_ID_58392 Human_SNP_ID_213099174 m1A Human chr4 + 168878321 168878321 168878321 TCGGCCACAGCCAGACGCCCGCGGCCTTCCTCAGCGCTCTGCTGCCCTCGCAGCCGCCGCCGGCG TCGGCCACAGCCAGACGCCCGCGGCCTTCCTCGGCGCTCTGCTGCCCTCGCAGCCGCCGCCGGCG A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:168878301..168878325 26863196 MeRIP-seq:(Medium) rs1032107869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_621791,Human_Splice_Rec_621811 RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 58393 RMVar_ID_58393 Human_SNP_ID_213130373 m1A Human chr4 + 169010195 169010195 169010195 CAACCGCGGTTCCAAAAAAAAAAAAAAGAAAAAAAAAGGCAAACCGCAAAAAAAAATAACGCCGC CAACCGCGGTTCCAAAAAAAAAAAAAAGAAAAGAAAAGGCAAACCGCAAAAAAAAATAACGCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:169010145..169010230 26863196 MeRIP-seq:(Medium) rs528754595 Functional Loss SNV dbSNP153 33..33 33 - - - 58394 RMVar_ID_58394 Human_SNP_ID_213130386 m1A Human chr4 + 169010220 169010220 169010220 AAGAAAAAAAAAGGCAAACCGCAAAAAAAAATAACGCCGCTCGACACCTCCTGCAGCCGCACAAT AAGAAAAAAAAAGGCAAACCGCAAAAAAAAATTACGCCGCTCGACACCTCCTGCAGCCGCACAAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:169010079..169010238 26863196 MeRIP-seq:(Medium) rs1211860401 Functional Loss SNV dbSNP153 33..33 33 - - - 58395 RMVar_ID_58395 Human_SNP_ID_213156888 m1A Human chr4 - 169117479 169117479 169117479 CCCAGGCCAGAACATATCAGGATAAAGGGCTTACCTGCCTAATAGTAGATCTTTTATGACAGATG CCCAGGCCAGAACATATCAGGATAAAGGGCTTTCCTGCCTAATAGTAGATCTTTTATGACAGATG T A SH3RF1 Ensembl:ENSG00000154447 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:169117475..169117591 26863196 MeRIP-seq:(Medium) rs1384169264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340285,RMVar_hsa_circ_69708,RMVar_hsa_circ_319074,RMVar_hsa_circ_25086,RMVar_hsa_circ_229495 58396 RMVar_ID_58396 Human_SNP_ID_213169860 m1A Human chr4 + 169175358 169175358 169175358 CAAACTCCTTCCTGTGGCTCCCAAGGCTTTCTATCATCTGGTCCCGGCTAACCTCTCTGGCTCCC CAAACTCCTTCCTGTGGCTCCCAAGGCTTTCTCTCATCTGGTCCCGGCTAACCTCTCTGGCTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:169175211..169175482 26863196 MeRIP-seq:(Medium) rs1249716071 Functional Loss SNV dbSNP153 33..33 33 - - - 58397 RMVar_ID_58397 Human_SNP_ID_213191058 m1A Human chr4 + 169270897 169270897 169270897 CCTCGGCTCCTCCTCTTTGTTCGCGGCCCCGCAGCGGCTGCGGCGGCTGATGCAGATGCGGCCCC CCTCGGCTCCTCCTCTTTGTTCGCGGCCCCGCGGCGGCTGCGGCGGCTGATGCAGATGCGGCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:169270860..169270989 26863196 MeRIP-seq:(Medium) rs1241780453 Functional Loss SNV dbSNP153 33..33 33 - - - 58398 RMVar_ID_58398 Human_SNP_ID_213259972 m1A Human chr4 - 169561556 169561556 169561556 GAAATGGTGTTTTGTTTATTTCTTTTCCCCAAAGTTGGAAAGAATAAATAGGGCCAGGGAACAAG GAAATGGTGTTTTGTTTATTTCTTTTCCCCAATGTTGGAAAGAATAAATAGGGCCAGGGAACAAG T A NEK1 Ensembl:ENSG00000137601 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:169561531..169561599;chr4:169561522..169561693 26863196 MeRIP-seq:(Medium) rs781260493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2832438,Human_RBP_ID_3732810 Human_Splice_Rec_622013,Human_Splice_Rec_622103,Human_Splice_Rec_622169,Human_Splice_Rec_622233,Human_Splice_Rec_622351 RMVar_hsa_circ_66227,RMVar_hsa_circ_57562,RMVar_hsa_circ_66616,RMVar_hsa_circ_122853,RMVar_hsa_circ_229505,RMVar_hsa_circ_18632,RMVar_hsa_circ_69567,RMVar_hsa_circ_365739,RMVar_hsa_circ_73308,RMVar_hsa_circ_354376,RMVar_hsa_circ_69461,RMVar_hsa_circ_324547,RMVar_hsa_circ_326220,RMVar_hsa_circ_10925,RMVar_hsa_circ_38601,RMVar_hsa_circ_29311,RMVar_hsa_circ_229524,RMVar_hsa_circ_229525,RMVar_hsa_circ_266448,RMVar_hsa_circ_352779,RMVar_hsa_circ_360661,RMVar_hsa_circ_367972,RMVar_hsa_circ_83241,RMVar_hsa_circ_104294,RMVar_hsa_circ_229527,RMVar_hsa_circ_229528,RMVar_hsa_circ_229529,RMVar_hsa_circ_265548,RMVar_hsa_circ_57536,RMVar_hsa_circ_70128,RMVar_hsa_circ_53315,RMVar_hsa_circ_229530 58399 RMVar_ID_58399 Human_SNP_ID_213306586 m1A Human chr4 - 169757767 169757767 169757767 GGGGCGCTTTGGGTGACAGCCAGGGCACCAGGAGGCAGCGCTTTTCATTCATCCAGTGACTATTA GGGGCGCTTTGGGTGACAGCCAGGGCACCAGGTGGCAGCGCTTTTCATTCATCCAGTGACTATTA T A HPF1 Ensembl:ENSG00000056050 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:169757764..169757922 26863196 MeRIP-seq:(Medium) rs1266284432 Functional Loss SNV dbSNP153 33..33 33 - - - 58400 RMVar_ID_58400 Human_SNP_ID_213306645 m1A Human chr4 - 169757853 169757853 169757853 GCTGCAGAATGGTCGGCGGTGGCGGGAAGCGCAGGCCCGGCGGAGAGGGGCCGCAGGTACTGCCG GCTGCAGAATGGTCGGCGGTGGCGGGAAGCGCCGGCCCGGCGGAGAGGGGCCGCAGGTACTGCCG T G HPF1 Ensembl:ENSG00000056050 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:169753810..169757927 26863196 MeRIP-seq:(Medium) rs1352801721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795180,Human_RBP_ID_27824516 Human_Splice_Rec_622539,Human_Splice_Rec_622555 58401 RMVar_ID_58401 Human_SNP_ID_213306667 m1A Human chr4 - 169757886 169757886 169757886 GGCCGCGGATCGGGGAATTCTGCTGGCGCTGCAGCTGCAGAATGGTCGGCGGTGGCGGGAAGCGC GGCCGCGGATCGGGGAATTCTGCTGGCGCTGCCGCTGCAGAATGGTCGGCGGTGGCGGGAAGCGC T G HPF1 Ensembl:ENSG00000056050 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:169753758..169757921 26863196 MeRIP-seq:(Medium) rs1204319869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795180 Human_Splice_Rec_622539,Human_Splice_Rec_622555 58402 RMVar_ID_58402 Human_SNP_ID_213372391 m1A Human chr4 - 170026314 170026314 170026314 GCCCGCAGTAGGCGCTACCGGGCGTCCGGCGCAGAGTGCGGCGCAGCGGCCGCTGTCGGGCTGGC GCCCGCAGTAGGCGCTACCGGGCGTCCGGCGCGGAGTGCGGCGCAGCGGCCGCTGTCGGGCTGGC T C MFAP3L Ensembl:ENSG00000198948 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:170026189..170026390 26863196 MeRIP-seq:(Medium) rs1410314565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_622601,Human_Splice_Rec_622605,Human_Splice_Rec_622611,Human_Splice_Rec_622625,Human_Splice_Rec_622629 58403 RMVar_ID_58403 Human_SNP_ID_213383918 m1A Human chr4 - 170072300 170072279 170072301 AAGACCCCAACTCTAAATATATATATATATATACACACACACATATATATACACACACACACATA AAGACCCCAACTCTAAATATATATATATATA______________________CACACACACATA GTGTATATATATGTGTGTGTGTA G AADAT Ensembl:ENSG00000109576 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:170072293..170072375 26863410 MeRIP-seq:(Medium) rs1227269927 Functional Loss DEL dbSNP153 32..53 33 - - - RMVar_hsa_circ_1471,RMVar_hsa_circ_63563,RMVar_hsa_circ_62645,RMVar_hsa_circ_229554,RMVar_hsa_circ_81680,RMVar_hsa_circ_34080 58404 RMVar_ID_58404 Human_SNP_ID_213383920 m1A Human chr4 - 170072300 170072281 170072301 AAGACCCCAACTCTAAATATATATATATATATACACACACACATATATATACACACACACACATA AAGACCCCAACTCTAAATATATATATATATA____________________CACACACACACATA GTATATATATGTGTGTGTGTA G AADAT Ensembl:ENSG00000109576 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:170072293..170072375 26863410 MeRIP-seq:(Medium) rs1196568889 Functional Loss DEL dbSNP153 32..51 33 - - - RMVar_hsa_circ_1471,RMVar_hsa_circ_63563,RMVar_hsa_circ_62645,RMVar_hsa_circ_229554,RMVar_hsa_circ_81680,RMVar_hsa_circ_34080 58405 RMVar_ID_58405 Human_SNP_ID_213388186 m1A Human chr4 - 170089730 170089730 170089730 TTGACGAGGCTCTTTGGTTTTTCTAGTCCTCAACCACTGAAGAAGAAGCTTGATGCTTGGCTGTC TTGACGAGGCTCTTTGGTTTTTCTAGTCCTCAGCCACTGAAGAAGAAGCTTGATGCTTGGCTGTC T C AADAT Ensembl:ENSG00000109576 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:170089679..170090197 26863196 MeRIP-seq:(Medium) rs1224307365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1974676,Human_RBP_ID_9396777 Human_Splice_Rec_622662,Human_Splice_Rec_622688,Human_Splice_Rec_622714,Human_Splice_Rec_622758,Human_Splice_Rec_622770 RMVar_hsa_circ_1471,RMVar_hsa_circ_62645,RMVar_hsa_circ_61568 58406 RMVar_ID_58406 Human_SNP_ID_213388231 m1A Human chr4 + 170089852 170089852 170089852 GCGTCTGGCTTCCCGCGCGCGGTGCCCGGAGAACGCCGCCGAAACTCCCCGGCTGGACGCTGCGT GCGTCTGGCTTCCCGCGCGCGGTGCCCGGAGAGCGCCGCCGAAACTCCCCGGCTGGACGCTGCGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:170089801..170090178 26863196 MeRIP-seq:(Medium) rs1292142489 Functional Loss SNV dbSNP153 33..33 33 - - - 58407 RMVar_ID_58407 Human_SNP_ID_213825213 m1A Human chr4 + 171813753 171813753 171813753 CAGAGGATCGCATTCCGAGGACCGCGCGAGGAAGGGACGTCGCGGCGCCACCACTTCCTGGCTGG CAGAGGATCGCATTCCGAGGACCGCGCGAGGAGGGGACGTCGCGGCGCCACCACTTCCTGGCTGG A G GALNTL6 Ensembl:ENSG00000174473 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:171813702..171813802 32194978 MeRIP-seq:(Medium) rs1230587010 Functional Loss SNV dbSNP153 33..33 33 - - - 58408 RMVar_ID_58408 Human_SNP_ID_214146826 m1A Human chr4 - 173168810 173168809 173168811 GCCTCATCTTCCTCCGGCGGCGAGAGACTCACAGCCCGGCGCAGCCGCCGCCACCGCTCTCCCCT GCCTCATCTTCCTCCGGCGGCGAGAGACTCA__GCCCGGCGCAGCCGCCGCCACCGCTCTCCCCT CTG C AC105285.1 Ensembl:ENSG00000245213 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:173168279..173169124 26863196 MeRIP-seq:(Medium) rs759193805 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8267159 58409 RMVar_ID_58409 Human_SNP_ID_214146977 m1A Human chr4 - 173169112 173169112 173169112 GGCCAGGGAGGTCGGAGTGCGCGGGGCTCGGCACCCCCTCGGCCCGCGCTGCGCCAGCACCACCT GGCCAGGGAGGTCGGAGTGCGCGGGGCTCGGCGCCCCCTCGGCCCGCGCTGCGCCAGCACCACCT T C AC105285.1 Ensembl:ENSG00000245213 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:173169106..173169405 26863196 MeRIP-seq:(Medium) rs1213543690 Functional Loss SNV dbSNP153 33..33 33 - - - 58410 RMVar_ID_58410 Human_SNP_ID_214147053 m1A Human chr4 + 173169280 173169271 173169280 CCGCGCCGGGACTGCGGGCGGAGCGGGCGGAGAGCCGGGTCCGGGGGGCTGCGGCCGCCCGGCGT CCGCGCCGGGACTGCGGGCGGAGC_________GCCGGGTCCGGGGGGCTGCGGCCGCCCGGCGT CGGGCGGAGA C GALNT7 Ensembl:ENSG00000109586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:173169276..173169424 26863196 MeRIP-seq:(Medium) rs1561138548 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_5241999 RMVar_hsa_circ_229566,RMVar_hsa_circ_75719 58411 RMVar_ID_58411 Human_SNP_ID_214148961 m1A Human chr4 - 173177388 173177388 173177388 ATCCACTTCTGATTCCATTCTGAGCTCCATCGACCTGGTTAAGACACCTTCACTTGACTGACCTG ATCCACTTCTGATTCCATTCTGAGCTCCATCGCCCTGGTTAAGACACCTTCACTTGACTGACCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:173177386..173177623 26863196 MeRIP-seq:(Medium) rs1212194645 Functional Loss SNV dbSNP153 33..33 33 - - - 58412 RMVar_ID_58412 Human_SNP_ID_214151027 m1A Human chr4 + 173183976 173183976 173183976 TCCTCACCTCCCAGACGGGGTCGCGGCCGGGCAGAGGCGCTCTTCACATCTCAGACGGGTCGGTG TCCTCACCTCCCAGACGGGGTCGCGGCCGGGCGGAGGCGCTCTTCACATCTCAGACGGGTCGGTG A G GALNT7 Ensembl:ENSG00000109586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:173183969..173184113 26863196 MeRIP-seq:(Medium) rs1357573576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229566,RMVar_hsa_circ_75719 58413 RMVar_ID_58413 Human_SNP_ID_214151231 m1A Human chr4 + 173184451 173184451 173184451 AAACCCCGTCTCCACCAAGAAATATGAAAACCAGTCAGGCATGGTGGCGCCCGCCTGCAATCCCA AAACCCCGTCTCCACCAAGAAATATGAAAACCTGTCAGGCATGGTGGCGCCCGCCTGCAATCCCA A T GALNT7 Ensembl:ENSG00000109586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:173184449..173184586 26863196 MeRIP-seq:(Medium) rs961106363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229566,RMVar_hsa_circ_75719 58414 RMVar_ID_58414 Human_SNP_ID_214165605 m1A Human chr4 + 173248030 173248030 173248030 GACCCCATGCCCAACCGAGGCGGCAATGGACTAGCTCCTGGGGAGGACAGATTCAAACCTGTGGT GACCCCATGCCCAACCGAGGCGGCAATGGACTGGCTCCTGGGGAGGACAGATTCAAACCTGTGGT A G GALNT7 Ensembl:ENSG00000109586 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:173247964..173248131 26863196 MeRIP-seq:(Medium) rs1212338198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1636435,Human_RBP_ID_4798022,Human_RBP_ID_8878168 Human_Splice_Rec_623046,Human_Splice_Rec_623056 RMVar_hsa_circ_77321,RMVar_hsa_circ_274981,RMVar_hsa_circ_229566,RMVar_hsa_circ_75719,RMVar_hsa_circ_229567,RMVar_hsa_circ_281207,RMVar_hsa_circ_114703,RMVar_hsa_circ_124046,RMVar_hsa_circ_94253,RMVar_hsa_circ_229569,RMVar_hsa_circ_229571,RMVar_hsa_circ_229572,RMVar_hsa_circ_229570,RMVar_hsa_circ_229573,RMVar_hsa_circ_229568 58415 RMVar_ID_58415 Human_SNP_ID_214180391 m1A Human chr4 - 173315215 173315215 173315215 GCCCTTATCCCTTCACACACCAACCCATAAGGAATCCACTCCCAGATGAACTATGCTTCCGCAGT GCCCTTATCCCTTCACACACCAACCCATAAGGCATCCACTCCCAGATGAACTATGCTTCCGCAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:173315164..173315299 26863196 MeRIP-seq:(Medium) rs554801362 Functional Loss SNV dbSNP153 33..33 33 - - - 58416 RMVar_ID_58416 Human_SNP_ID_214183354 m1A Human chr4 - 173328734 173328734 173328734 ATGGTGGTGCATGCCTGTGGTCCTGGCTATTTAGGAGGCTGAGGTGGATCACTTGAGCCTGGGAT ATGGTGGTGCATGCCTGTGGTCCTGGCTATTTGGGAGGCTGAGGTGGATCACTTGAGCCTGGGAT T C AC097534.1 Ensembl:ENSG00000248774 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1490209946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7287694 58417 RMVar_ID_58417 Human_SNP_ID_214184417 m1A Human chr4 - 173332141 173332141 173332141 AGGCTCAAAGAAGAAGAACGAACCAGAAGATGAGGAGGAGGAGGAGGAAGAAGAAGATGAAGATG AGGCTCAAAGAAGAAGAACGAACCAGAAGATGGGGAGGAGGAGGAGGAAGAAGAAGATGAAGATG T C HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:173331776..173332289 32194978 MeRIP-seq:(Medium) rs1409172017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213854,Human_RBP_ID_249141,Human_RBP_ID_616761,Human_RBP_ID_837637,Human_RBP_ID_941783,Human_RBP_ID_1636472,Human_RBP_ID_2832969,Human_RBP_ID_3733074,Human_RBP_ID_5607331,Human_RBP_ID_7287802,Human_RBP_ID_8265742,Human_RBP_ID_9396782,Human_RBP_ID_17662032,Human_RBP_ID_18536957,Human_RBP_ID_21022600,Human_RBP_ID_22008826,Human_RBP_ID_22095735,Human_RBP_ID_22510449,Human_RBP_ID_23034748,Human_RBP_ID_23116084,Human_RBP_ID_23120107,Human_RBP_ID_24045074,Human_RBP_ID_24547746,Human_RBP_ID_26349650,Human_RBP_ID_27824532 Human_Splice_Rec_623124,Human_Splice_Rec_623130,Human_Splice_Rec_623138 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578 58418 RMVar_ID_58418 Human_SNP_ID_214184420 m1A Human chr4 - 173332153 173332153 173332153 TGGCAGGCCAACAGGCTCAAAGAAGAAGAACGAACCAGAAGATGAGGAGGAGGAGGAGGAAGAAG TGGCAGGCCAACAGGCTCAAAGAAGAAGAACGGACCAGAAGATGAGGAGGAGGAGGAGGAAGAAG T C HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:173332026..173332257 26863196 MeRIP-seq:(Medium) rs762867578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_616761,Human_RBP_ID_837637,Human_RBP_ID_941783,Human_RBP_ID_1035793,Human_RBP_ID_1636472,Human_RBP_ID_2832969,Human_RBP_ID_4798052,Human_RBP_ID_7287802,Human_RBP_ID_8265742,Human_RBP_ID_8587289,Human_RBP_ID_9396782,Human_RBP_ID_15096342,Human_RBP_ID_17662032,Human_RBP_ID_18536957,Human_RBP_ID_22095735,Human_RBP_ID_22510449,Human_RBP_ID_23034748,Human_RBP_ID_23116084,Human_RBP_ID_23120107,Human_RBP_ID_24045074,Human_RBP_ID_24547748,Human_RBP_ID_26349651,Human_RBP_ID_27824533 Human_Splice_Rec_623124,Human_Splice_Rec_623130,Human_Splice_Rec_623138 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578 58419 RMVar_ID_58419 Human_SNP_ID_214184430 m1A Human chr4 - 173332165 173332165 173332165 AAAGAAGGGCCCTGGCAGGCCAACAGGCTCAAAGAAGAAGAACGAACCAGAAGATGAGGAGGAGG AAAGAAGGGCCCTGGCAGGCCAACAGGCTCAAGGAAGAAGAACGAACCAGAAGATGAGGAGGAGG T C HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:173332065..173332195 26863196 MeRIP-seq:(Medium) rs1370393541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_616782,Human_RBP_ID_786241,Human_RBP_ID_941783,Human_RBP_ID_1035793,Human_RBP_ID_1636473,Human_RBP_ID_2832970,Human_RBP_ID_4798052,Human_RBP_ID_7287804,Human_RBP_ID_8587289,Human_RBP_ID_9396783,Human_RBP_ID_15096342,Human_RBP_ID_22510450,Human_RBP_ID_23034748,Human_RBP_ID_23116084,Human_RBP_ID_23120107,Human_RBP_ID_24045076,Human_RBP_ID_24547749,Human_RBP_ID_26349651,Human_RBP_ID_27824533 Human_Splice_Rec_623124,Human_Splice_Rec_623130,Human_Splice_Rec_623138 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578 58420 RMVar_ID_58420 Human_SNP_ID_214184611 m1A Human chr4 + 173332803 173332801 173332803 ATTACCTATACCTAGTCTTATCCACGGCTTTAAAAAAGATGACACTGTACCTTTTCATATTTCTC ATTACCTATACCTAGTCTTATCCACGGCTTT__AAAAGATGACACTGTACCTTTTCATATTTCTC TAA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:173332801..173332933 26863196 MeRIP-seq:(Medium) rs779920500 Functional Loss DEL dbSNP153 32..33 33 - - - 58421 RMVar_ID_58421 Human_SNP_ID_214184628 m1A Human chr4 - 173332914 173332914 173332914 GAACACCCTGGCCTATCCATTGGGGATACTGCAAAGAAATTGGGTGAAATGTGGTCTGAGCAGTC GAACACCCTGGCCTATCCATTGGGGATACTGCGAAGAAATTGGGTGAAATGTGGTCTGAGCAGTC T C HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:173332801..173333000 32194978 MeRIP-seq:(Medium) rs1216205723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_616789,Human_RBP_ID_1035798,Human_RBP_ID_1106362,Human_RBP_ID_1636476,Human_RBP_ID_1974761,Human_RBP_ID_3733077,Human_RBP_ID_4777959,Human_RBP_ID_7287819,Human_RBP_ID_8587293,Human_RBP_ID_9152992,Human_RBP_ID_9396786,Human_RBP_ID_15096368,Human_RBP_ID_18022067,Human_RBP_ID_18820816,Human_RBP_ID_22825732,Human_RBP_ID_24045096,Human_RBP_ID_26349654,Human_RBP_ID_26826078,Human_RBP_ID_27064103,Human_RBP_ID_27725695,Human_RBP_ID_27824539 Human_Splice_Rec_623122,Human_Splice_Rec_623123,Human_Splice_Rec_623128,Human_Splice_Rec_623129,Human_Splice_Rec_623136,Human_Splice_Rec_623137,Human_Splice_Rec_623146 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578,RMVar_hsa_circ_229579,RMVar_hsa_circ_283352 58422 RMVar_ID_58422 Human_SNP_ID_214184698 m1A Human chr4 - 173333165 173333165 173333165 GAAGTCGAAGTTTGAAGATATGGCAAAAAGTGACAAAGCTCGCTATGACAGGGAGATGAAAAATT GAAGTCGAAGTTTGAAGATATGGCAAAAAGTGCCAAAGCTCGCTATGACAGGGAGATGAAAAATT T G HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs200502763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283217,Human_RBP_ID_941099,Human_RBP_ID_1636481,Human_RBP_ID_1974764,Human_RBP_ID_4777966,Human_RBP_ID_7287824,Human_RBP_ID_8587299,Human_RBP_ID_8878207,Human_RBP_ID_9152993,Human_RBP_ID_9396791,Human_RBP_ID_15096379,Human_RBP_ID_17294130,Human_RBP_ID_18032232,Human_RBP_ID_18447357,Human_RBP_ID_24045099,Human_RBP_ID_25829920,Human_RBP_ID_26348936,Human_RBP_ID_27825180 Human_Splice_Rec_623120,Human_Splice_Rec_623121,Human_Splice_Rec_623126,Human_Splice_Rec_623127,Human_Splice_Rec_623134,Human_Splice_Rec_623135,Human_Splice_Rec_623140,Human_Splice_Rec_623144,Human_Splice_Rec_623145 Human_miRNA_ID_2443625 RMVar_hsa_circ_44926,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577 58423 RMVar_ID_58423 Human_SNP_ID_214185103 m1A Human chr4 + 173334303 173334303 173334303 CCTGGTGCGAGCTTTTCCTCAGAGTCCCGCAGAGCGGCCGGACCCAACGGAGACGCTTCCCTCAC CCTGGTGCGAGCTTTTCCTCAGAGTCCCGCAGGGCGGCCGGACCCAACGGAGACGCTTCCCTCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:173334301..173334350 32194978 MeRIP-seq:(Medium) rs918128142 Functional Loss SNV dbSNP153 33..33 33 - - - 58424 RMVar_ID_58424 Human_SNP_ID_214185122 m1A Human chr4 - 173334327 173334327 173334327 TAAACCAGTTCACGCCGGAGCCCCGTGAGGGAAGCGTCTCCGTTGGGTCCGGCCGCTCTGCGGGA TAAACCAGTTCACGCCGGAGCCCCGTGAGGGAGGCGTCTCCGTTGGGTCCGGCCGCTCTGCGGGA T C HMGB2 Ensembl:ENSG00000164104 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1245513904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249145,Human_RBP_ID_616803,Human_RBP_ID_785572,Human_RBP_ID_1636494,Human_RBP_ID_4794756,Human_RBP_ID_8587307,Human_RBP_ID_9334827,Human_RBP_ID_9397509,Human_RBP_ID_18424650,Human_RBP_ID_22095740,Human_RBP_ID_22825743,Human_RBP_ID_26348939,Human_RBP_ID_27064113 Human_Splice_Rec_623131 RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_17556 58425 RMVar_ID_58425 Human_SNP_ID_214193748 m1A Human chr4 + 173371451 173371451 173371451 GGCAGGCAACGCCAGCTTCAGCAAGAGGATCCAGAAGAGCATCTCCCAGAAGAAGGTGAAGATCG GGCAGGCAACGCCAGCTTCAGCAAGAGGATCCCGAAGAGCATCTCCCAGAAGAAGGTGAAGATCG A C SAP30 Ensembl:ENSG00000164105 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:173371276..173371450 32194978 MeRIP-seq:(Medium) rs568734277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941103,Human_RBP_ID_7287850,Human_RBP_ID_26350411,Human_RBP_ID_27824542 Human_Splice_Rec_623167 58426 RMVar_ID_58426 Human_SNP_ID_214233602 m1A Human chr4 - 173527251 173527251 173527251 GCAGTGAGGAGGAGGAGAAGGAGGAGGAGGAGAGCGCGAGTGAGCAGGGGCCAAGGCGCCAGATG GCAGTGAGGAGGAGGAGAAGGAGGAGGAGGAGGGCGCGAGTGAGCAGGGGCCAAGGCGCCAGATG T C HAND2 Ensembl:ENSG00000164107 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:173527200..173527307 32194978 MeRIP-seq:(Medium) rs1553974383 Functional Loss SNV dbSNP153 33..33 33 - - - 58427 RMVar_ID_58427 Human_SNP_ID_214415996 m1A Human chr4 - 174263084 174263084 174263084 TCTGGCTTTTTCCCAGGCTTGCAGATGGGTCAAGGGTTGTGGAGAGTGGTCAGAAACCAGCAGCT TCTGGCTTTTTCCCAGGCTTGCAGATGGGTCAGGGGTTGTGGAGAGTGGTCAGAAACCAGCAGCT T C FBXO8 Ensembl:ENSG00000164117 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:174263033..174269086 32194978 MeRIP-seq:(Medium) rs776076785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1636568,Human_RBP_ID_4795711,Human_RBP_ID_24045422,Human_RBP_ID_26350414 Human_Splice_Rec_623710,Human_Splice_Rec_623720,Human_Splice_Rec_623730 RMVar_hsa_circ_279734,RMVar_hsa_circ_229589,RMVar_hsa_circ_360528 58428 RMVar_ID_58428 Human_SNP_ID_214924660 m1A Human chr4 - 176320072 176320072 176320072 AGTTCGCCCGCGACAGCACCGTGTTCATCGCGATCGTCTCCCACGAGTCCGGACTCCACACGCAC AGTTCGCCCGCGACAGCACCGTGTTCATCGCGGTCGTCTCCCACGAGTCCGGACTCCACACGCAC T C AC019163.1 Ensembl:ENSG00000248980 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr4:176311568..176320271;chr4:176320001..176320458 32194978 MeRIP-seq:(Medium) rs777553804 Functional Loss SNV dbSNP153 33..33 33 - - - 58429 RMVar_ID_58429 Human_SNP_ID_215042400 m1A Human chr4 + 176792459 176792459 176792459 CGACCCCCCCTGGGCGAGCCGGAGGCGGCGGGAGCGGGTCCGGGGCTCCGCGTTCCCAACTTTGC CGACCCCCCCTGGGCGAGCCGGAGGCGGCGGGTGCGGGTCCGGGGCTCCGCGTTCCCAACTTTGC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:176792380..176792628 26863410 MeRIP-seq:(Medium) rs1006997100 Functional Loss SNV dbSNP153 33..33 33 - - - 58430 RMVar_ID_58430 Human_SNP_ID_215178217 m1A Human chr4 - 177351510 177351510 177351510 CCTTGAGGTCAAGCAAGCATCACATGCCTTAGAAGAGGGCTTATTGATTAAAGTACACACCACAC CCTTGAGGTCAAGCAAGCATCACATGCCTTAGGAGAGGGCTTATTGATTAAAGTACACACCACAC T C AC027627.1 Ensembl:ENSG00000249084 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:177341592..177351527 32194978 MeRIP-seq:(Medium) rs746576745 Functional Loss SNV dbSNP153 33..33 33 - - - 58431 RMVar_ID_58431 Human_SNP_ID_215200497 m1A Human chr4 - 177442366 177442366 177442366 GCTGGTCTCTTCGGTGGTCAGGGATGGCGCGGAAGTCGAACTTGCCTGTGCTTCTCGTGCCGTTT GCTGGTCTCTTCGGTGGTCAGGGATGGCGCGGCAGTCGAACTTGCCTGTGCTTCTCGTGCCGTTT T G AGA Ensembl:ENSG00000038002 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:177442292..177442458;chr4:177442289..177442404 26863196 MeRIP-seq:(Medium) rs149092606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794763 58432 RMVar_ID_58432 Human_SNP_ID_391577725 m1A Human chr9 - 15466796 15466796 15466796 TCAAGATGGTAATCAGCCACAACATAACGGGGAGAGCAATGAAGACAGCAAAGACAACCATGAAG TCAAGATGGTAATCAGCCACAACATAACGGGGCGAGCAATGAAGACAGCAAAGACAACCATGAAG T G PSIP1 Ensembl:ENSG00000164985 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:15466726..15466850 26863196 MeRIP-seq:(Medium) rs201652868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91602,Human_RBP_ID_256188,Human_RBP_ID_26360594 Human_Splice_Rec_1033692,Human_Splice_Rec_1033693,Human_Splice_Rec_1033722,Human_Splice_Rec_1033723 RMVar_hsa_circ_59570,RMVar_hsa_circ_98452,RMVar_hsa_circ_114356,RMVar_hsa_circ_255823,RMVar_hsa_circ_87910,RMVar_hsa_circ_255824,RMVar_hsa_circ_255822 58433 RMVar_ID_58433 Human_SNP_ID_391578574 m1A Human chr9 - 15469057 15469057 15469057 ACAGCTATGAAATTACTGTTTTGTCATGAAGGATGTGAACAGATGCATTGAGGCCTTGGATGAAC ACAGCTATGAAATTACTGTTTTGTCATGAAGGTTGTGAACAGATGCATTGAGGCCTTGGATGAAC T A PSIP1 Ensembl:ENSG00000164985 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:15469006..15469313 32194978 MeRIP-seq:(Medium) rs536287269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2062731,Human_RBP_ID_24522988 Human_Splice_Rec_1033688,Human_Splice_Rec_1033718 RMVar_hsa_circ_98452,RMVar_hsa_circ_114356,RMVar_hsa_circ_255823,RMVar_hsa_circ_255822,RMVar_hsa_circ_107121,RMVar_hsa_circ_22326,RMVar_hsa_circ_60934,RMVar_hsa_circ_117253,RMVar_hsa_circ_255826,RMVar_hsa_circ_255827 58434 RMVar_ID_58434 Human_SNP_ID_391580403 m1A Human chr9 + 15474060 15474060 15474060 TCTCCTTCTTCTTCAGAATCGGAGGTTGAAGTAACCCCTGTTTTAGCTAAATTTTTCCTTTTTGA TCTCCTTCTTCTTCAGAATCGGAGGTTGAAGTGACCCCTGTTTTAGCTAAATTTTTCCTTTTTGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:15472668..15485916 32194978 MeRIP-seq:(Medium) rs767758501 Functional Loss SNV dbSNP153 33..33 33 - - - 58435 RMVar_ID_58435 Human_SNP_ID_391584303 m1A Human chr9 - 15486773 15486773 15486773 ATTTTAAACCCATTTTGTTTCAAGGAAGAAATAATGAAATGAGTTGGCCATGATTAATTAGTAAG ATTTTAAACCCATTTTGTTTCAAGGAAGAAATCATGAAATGAGTTGGCCATGATTAATTAGTAAG T G PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:15486771..15486845 26863196 MeRIP-seq:(Medium) rs1186794104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46716,RMVar_hsa_circ_114356,RMVar_hsa_circ_255822,RMVar_hsa_circ_107121,RMVar_hsa_circ_61773,RMVar_hsa_circ_255827,RMVar_hsa_circ_321676,RMVar_hsa_circ_313857,RMVar_hsa_circ_315873,RMVar_hsa_circ_316557,RMVar_hsa_circ_277408 58436 RMVar_ID_58436 Human_SNP_ID_391592303 m1A Human chr9 - 15510103 15510103 15510103 TCCCCATTGGCCAGCTCGAGTAAGTGATTTGTAGCCCTCGCGCTTAGCAGTGCTACCCTCCTCTC TCCCCATTGGCCAGCTCGAGTAAGTGATTTGTGGCCCTCGCGCTTAGCAGTGCTACCCTCCTCTC T C PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:15510101..15510150 32194978 MeRIP-seq:(Medium) rs758794961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16629795 58437 RMVar_ID_58437 Human_SNP_ID_391592369 m1A Human chr9 + 15510224 15510224 15510224 TCGGGGGCGAGACCGGGGGTCCGAAGCCCGGGAGGCGGCGAGGAGATGCGGCGGCGCGGGGATGC TCGGGGGCGAGACCGGGGGTCCGAAGCCCGGGGGGCGGCGAGGAGATGCGGCGGCGCGGGGATGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:15510176..15510250 26863196 MeRIP-seq:(Medium) rs1563906243 Functional Loss SNV dbSNP153 33..33 33 - - - 58438 RMVar_ID_58438 Human_SNP_ID_391592654 m1A Human chr9 - 15510729 15510729 15510729 TGTAGCGGGGAAGTGGACGCGGCCCGCCCGGGAGCCGAGGGGGCCGAGGCTGCAGCCGCTGGGCA TGTAGCGGGGAAGTGGACGCGGCCCGCCCGGGGGCCGAGGGGGCCGAGGCTGCAGCCGCTGGGCA T C PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:15510718..15510975 26863196 MeRIP-seq:(Medium) rs1368107265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963040 58439 RMVar_ID_58439 Human_SNP_ID_391592679 m1A Human chr9 + 15510781 15510780 15510781 CTTCCCCGCTACAGCCAGGAGCGACGCCACCGAGGGGGGGGCGGGGCGAGTCCCCGTCGCCCGCT CTTCCCCGCTACAGCCAGGAGCGACGCCACCG_GGGGGGGGCGGGGCGAGTCCCCGTCGCCCGCT GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:15510779..15510975 26863196 MeRIP-seq:(Medium) rs993588841 Functional Loss DEL dbSNP153 33..33 33 - - - 58440 RMVar_ID_58440 Human_SNP_ID_391592717 m1A Human chr9 - 15510851 15510851 15510851 GCTTGCGTGGACGCGGGTAGAGGCGACCGGCCAGCAACCGCAGCGTCGGCGCCCGCGGCCCCGGC GCTTGCGTGGACGCGGGTAGAGGCGACCGGCCGGCAACCGCAGCGTCGGCGCCCGCGGCCCCGGC T C PSIP1 Ensembl:ENSG00000164985 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:15510819..15510919 26863410 MeRIP-seq:(Medium) rs1463715597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_716397,Human_RBP_ID_5023831,Human_RBP_ID_9314952,Human_RBP_ID_9338880 Human_Splice_Rec_1033665,Human_Splice_Rec_1033695,Human_Splice_Rec_1033725,Human_Splice_Rec_1033745,Human_Splice_Rec_1033795,Human_Splice_Rec_1033803,Human_Splice_Rec_1033809 58441 RMVar_ID_58441 Human_SNP_ID_391597964 m1A Human chr9 - 15527719 15527719 15527719 CCAAGGCCCCCGCCGCAGCTCCAGCGCCGCGCAGCAGCCGCCGCCGCCGCCTCTCCTTAGTCACT CCAAGGCCCCCGCCGCAGCTCCAGCGCCGCGCGGCAGCCGCCGCCGCCGCCTCTCCTTAGTCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:15527671..15527810 26863196 MeRIP-seq:(Medium) rs1026192249 Functional Loss SNV dbSNP153 33..33 33 - - - 58442 RMVar_ID_58442 Human_SNP_ID_391606483 m1A Human chr9 - 15553114 15553114 15553114 CAAAGGGGTACAGAAGGGGAAGAGCCCCCGGGAGGTGAAGTTTACAACTGCCACTTCCGGAGCTG CAAAGGGGTACAGAAGGGGAAGAGCCCCCGGGTGGTGAAGTTTACAACTGCCACTTCCGGAGCTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:15553022..15553115 26863196 MeRIP-seq:(Medium) rs1332683446 Functional Loss SNV dbSNP153 33..33 33 - - - 58443 RMVar_ID_58443 Human_SNP_ID_391606484 m1A Human chr9 - 15553114 15553114 15553114 CAAAGGGGTACAGAAGGGGAAGAGCCCCCGGGAGGTGAAGTTTACAACTGCCACTTCCGGAGCTG CAAAGGGGTACAGAAGGGGAAGAGCCCCCGGGCGGTGAAGTTTACAACTGCCACTTCCGGAGCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:15553022..15553115 26863196 MeRIP-seq:(Medium) rs1332683446 Functional Loss SNV dbSNP153 33..33 33 - - - 58444 RMVar_ID_58444 Human_SNP_ID_391875389 m1A Human chr9 - 16416997 16416997 16416997 TTCATCAGTCTAAAAGTTAGAAATATCCCTTTATTTTAACTTTTATGTCGTTTCCATTTTTCATG TTCATCAGTCTAAAAGTTAGAAATATCCCTTTTTTTTAACTTTTATGTCGTTTCCATTTTTCATG T A BNC2 Ensembl:ENSG00000173068 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1999032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_299278,Human_miRNA_ID_1754841 GWAS_ID_6834 58445 RMVar_ID_58445 Human_SNP_ID_391875390 m1A Human chr9 - 16416997 16416997 16416997 TTCATCAGTCTAAAAGTTAGAAATATCCCTTTATTTTAACTTTTATGTCGTTTCCATTTTTCATG TTCATCAGTCTAAAAGTTAGAAATATCCCTTTGTTTTAACTTTTATGTCGTTTCCATTTTTCATG T C BNC2 Ensembl:ENSG00000173068 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1999032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_299278,Human_miRNA_ID_1754841 GWAS_ID_6834 58446 RMVar_ID_58446 Human_SNP_ID_391875391 m1A Human chr9 - 16416997 16416997 16416997 TTCATCAGTCTAAAAGTTAGAAATATCCCTTTATTTTAACTTTTATGTCGTTTCCATTTTTCATG TTCATCAGTCTAAAAGTTAGAAATATCCCTTTCTTTTAACTTTTATGTCGTTTCCATTTTTCATG T G BNC2 Ensembl:ENSG00000173068 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1999032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_299278,Human_miRNA_ID_1754841 GWAS_ID_6834 58447 RMVar_ID_58447 Human_SNP_ID_391966798 m1A Human chr9 - 16726986 16726986 16726986 CCGACGTGGTAGCGCGAGGCCATCGGTTACTGATAATTAATCACCGGAGCCGGCGGCTCGTACCA CCGACGTGGTAGCGCGAGGCCATCGGTTACTGGTAATTAATCACCGGAGCCGGCGGCTCGTACCA T C BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:16726935..16727280 26863196 MeRIP-seq:(Medium) rs1428593075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18133328 RMVar_hsa_circ_97342,RMVar_hsa_circ_290021,RMVar_hsa_circ_298080,RMVar_hsa_circ_255850,RMVar_hsa_circ_346576,RMVar_hsa_circ_359137,RMVar_hsa_circ_255851,RMVar_hsa_circ_124556,RMVar_hsa_circ_98138,RMVar_hsa_circ_255853,RMVar_hsa_circ_83637,RMVar_hsa_circ_255852,RMVar_hsa_circ_255854,RMVar_hsa_circ_255855 58448 RMVar_ID_58448 Human_SNP_ID_391966888 m1A Human chr9 + 16727170 16727170 16727170 GGAGAGCGGGCCGGAGCCGGCGAAGGGAATGCAGGGGCGGGCGCAGAGGGCTGGCTGGCAAGGAG GGAGAGCGGGCCGGAGCCGGCGAAGGGAATGCCGGGGCGGGCGCAGAGGGCTGGCTGGCAAGGAG A C BNC2-AS1 Ensembl:ENSG00000234779 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:16726844..16727273 26863196 MeRIP-seq:(Medium) rs1227656913 Functional Loss SNV dbSNP153 33..33 33 - - - 58449 RMVar_ID_58449 Human_SNP_ID_391966889 m1A Human chr9 + 16727170 16727170 16727170 GGAGAGCGGGCCGGAGCCGGCGAAGGGAATGCAGGGGCGGGCGCAGAGGGCTGGCTGGCAAGGAG GGAGAGCGGGCCGGAGCCGGCGAAGGGAATGCGGGGGCGGGCGCAGAGGGCTGGCTGGCAAGGAG A G BNC2-AS1 Ensembl:ENSG00000234779 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:16726844..16727273 26863196 MeRIP-seq:(Medium) rs1227656913 Functional Loss SNV dbSNP153 33..33 33 - - - 58450 RMVar_ID_58450 Human_SNP_ID_391970183 m1A Human chr9 - 16738481 16738481 16738481 GTAATTTCCTTTCCCAATCTCTCAATAGGCACACCTTGGGCCCACCCCACCTCCACATAGCCTTA GTAATTTCCTTTCCCAATCTCTCAATAGGCACGCCTTGGGCCCACCCCACCTCCACATAGCCTTA T C BNC2 Ensembl:ENSG00000173068 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:16738453..16738548 26863196 MeRIP-seq:(Medium) rs745890218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1033960,Human_Splice_Rec_1033972,Human_Splice_Rec_1034018,Human_Splice_Rec_1034066 RMVar_hsa_circ_97342,RMVar_hsa_circ_298080,RMVar_hsa_circ_255850,RMVar_hsa_circ_359137,RMVar_hsa_circ_124556,RMVar_hsa_circ_98138,RMVar_hsa_circ_255853,RMVar_hsa_circ_255854,RMVar_hsa_circ_255857,RMVar_hsa_circ_109082,RMVar_hsa_circ_255855,RMVar_hsa_circ_274134,RMVar_hsa_circ_255859,RMVar_hsa_circ_255856,RMVar_hsa_circ_374026 58451 RMVar_ID_58451 Human_SNP_ID_391970186 m1A Human chr9 - 16738487 16738487 16738487 GCATATGTAATTTCCTTTCCCAATCTCTCAATAGGCACACCTTGGGCCCACCCCACCTCCACATA GCATATGTAATTTCCTTTCCCAATCTCTCAATGGGCACACCTTGGGCCCACCCCACCTCCACATA T C BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:16738469..16738537 26863196 MeRIP-seq:(Medium) rs780187588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109082,RMVar_hsa_circ_255856 58452 RMVar_ID_58452 Human_SNP_ID_391970187 m1A Human chr9 - 16738487 16738487 16738487 GCATATGTAATTTCCTTTCCCAATCTCTCAATAGGCACACCTTGGGCCCACCCCACCTCCACATA GCATATGTAATTTCCTTTCCCAATCTCTCAATCGGCACACCTTGGGCCCACCCCACCTCCACATA T G BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:16738469..16738537 26863196 MeRIP-seq:(Medium) rs780187588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109082,RMVar_hsa_circ_255856 58453 RMVar_ID_58453 Human_SNP_ID_392098496 m1A Human chr9 + 17135175 17135175 17135175 GCGGGGAGCTGAAGTACACGCAATGCGCAGCGAGGCCTCGGGTTTTGCCGGCGCAGCGCGGGAGG GCGGGGAGCTGAAGTACACGCAATGCGCAGCGGGGCCTCGGGTTTTGCCGGCGCAGCGCGGGAGG A G CNTLN Ensembl:ENSG00000044459 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:17135124..17135241 32194978 MeRIP-seq:(Medium) rs1229702534 Functional Loss SNV dbSNP153 33..33 33 - - - 58454 RMVar_ID_58454 Human_SNP_ID_392098544 m1A Human chr9 + 17135245 17135245 17135245 GCGGACGAAAGTGATAAAATCTGGGTGGGTGAAGAAGGGTCAGGGGGCCGGCGAGGGCCTGGGGG GCGGACGAAAGTGATAAAATCTGGGTGGGTGAGGAAGGGTCAGGGGGCCGGCGAGGGCCTGGGGG A G CNTLN Ensembl:ENSG00000044459 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:17135150..17135330 26863196 MeRIP-seq:(Medium) rs1385472486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92231,Human_RBP_ID_256506,Human_RBP_ID_963041,Human_RBP_ID_18133355,Human_RBP_ID_19023715 58455 RMVar_ID_58455 Human_SNP_ID_392098552 m1A Human chr9 + 17135254 17135253 17135255 AGTGATAAAATCTGGGTGGGTGAAGAAGGGTCAGGGGGCCGGCGAGGGCCTGGGGGGGCAGCTCC AGTGATAAAATCTGGGTGGGTGAAGAAGGGTC__GGGGCCGGCGAGGGCCTGGGGGGGCAGCTCC CAG C CNTLN Ensembl:ENSG00000044459 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:17135063..17135362 26863196 MeRIP-seq:(Medium) rs772777501 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_92231,Human_RBP_ID_256506,Human_RBP_ID_963041,Human_RBP_ID_19023715 58456 RMVar_ID_58456 Human_SNP_ID_392098634 m1A Human chr9 + 17135369 17135354 17135369 GCATCTCGGTAGAGGAGGCGATGGTGACCCGGACGCAGCTGCTGGAGGAAGAGCTGAGCAGCCTA GCATCTCGGTAGAGGAGG_______________CGCAGCTGCTGGAGGAAGAGCTGAGCAGCCTA GCGATGGTGACCCGGA G CNTLN Ensembl:ENSG00000044459 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:17135044..17143342;chr9:17135070..17135462 26863196 MeRIP-seq:(Medium) rs1283386622 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_7911936,Human_RBP_ID_16630921,Human_RBP_ID_19023715 Human_Splice_Rec_1034115,Human_Splice_Rec_1034119,Human_Splice_Rec_1034129 58457 RMVar_ID_58457 Human_SNP_ID_392140609 m1A Human chr9 + 17273733 17273733 17273733 TTTGATTATTGATATAAGCACTCTAATTTTAGACCTTTGAAGACAATTTAATTGAAGCAAGGAAA TTTGATTATTGATATAAGCACTCTAATTTTAGGCCTTTGAAGACAATTTAATTGAAGCAAGGAAA A G CNTLN Ensembl:ENSG00000044459 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3808795 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1034128,Human_Splice_Rec_1034138 GWAS_ID_6835,GWAS_ID_6836,GWAS_ID_6837,GWAS_ID_6838,GWAS_ID_6839,GWAS_ID_6840,GWAS_ID_6841,GWAS_ID_6842,GWAS_ID_6843,GWAS_ID_6844,GWAS_ID_6845,GWAS_ID_6846,GWAS_ID_6847,GWAS_ID_6848,GWAS_ID_6849,GWAS_ID_6850,GWAS_ID_6851,GWAS_ID_6852 RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_304454,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_301881,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255862 58458 RMVar_ID_58458 Human_SNP_ID_392147826 m1A Human chr9 + 17294680 17294680 17294680 TGGAGCTGCCTGCCAGTCCCGTGCCCTCCACCAGCACTCCTCAGCCCTTGGATGGGACTGGCTGC TGGAGCTGCCTGCCAGTCCCGTGCCCTCCACCGGCACTCCTCAGCCCTTGGATGGGACTGGCTGC A G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:17294652..17294741 26863196 MeRIP-seq:(Medium) rs897211741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58459 RMVar_ID_58459 Human_SNP_ID_392147827 m1A Human chr9 + 17294680 17294680 17294680 TGGAGCTGCCTGCCAGTCCCGTGCCCTCCACCAGCACTCCTCAGCCCTTGGATGGGACTGGCTGC TGGAGCTGCCTGCCAGTCCCGTGCCCTCCACCTGCACTCCTCAGCCCTTGGATGGGACTGGCTGC A T CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:17294652..17294741 26863196 MeRIP-seq:(Medium) rs897211741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58460 RMVar_ID_58460 Human_SNP_ID_392147927 m1A Human chr9 + 17294818 17294810 17294818 GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAAGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGGAGGGGGGGAGGGTGGGGGGGAG________GGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GTGGGCGAA G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:17294732..17294859 26863196 MeRIP-seq:(Medium) rs1203434122 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58461 RMVar_ID_58461 Human_SNP_ID_392147934 m1A Human chr9 + 17294818 17294813 17294818 GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAAGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGGAGGGGGGGAGGGTGGGGGGGAGTGG_____GGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGCGAA G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:17294732..17294859 26863196 MeRIP-seq:(Medium) rs1563967160 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58462 RMVar_ID_58462 Human_SNP_ID_392147936 m1A Human chr9 + 17294818 17294814 17294818 GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAAGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGGAGGGGGGGAGGGTGGGGGGGAGTGGG____GGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GCGAA G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:17294732..17294859 26863196 MeRIP-seq:(Medium) rs1563967170 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58463 RMVar_ID_58463 Human_SNP_ID_392147942 m1A Human chr9 + 17294818 17294816 17294818 GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAAGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCG__GGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GAA G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:17294732..17294859 26863196 MeRIP-seq:(Medium) rs1563967198 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58464 RMVar_ID_58464 Human_SNP_ID_392147947 m1A Human chr9 + 17294818 17294818 17294818 GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAAGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG GGGAGGGGGGGAGGGTGGGGGGGAGTGGGCGAGGGGGGGAGGGCGGGGAGGAGGGGGGAGGGCGG A G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:17294732..17294859 26863196 MeRIP-seq:(Medium) rs1171029031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255863,RMVar_hsa_circ_255862 58465 RMVar_ID_58465 Human_SNP_ID_392209012 m1A Human chr9 - 17503513 17503510 17503513 AAGTTGAGTGCAGAGTATTCTAGAAAGAGAGAAGACCAAGGGCAAATGTGGGAGGCAGGCACCAG AAGTTGAGTGCAGAGTATTCTAGAAAGAGAGA___CCAAGGGCAAATGTGGGAGGCAGGCACCAG GTCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:17503468..17503543 26863196 MeRIP-seq:(Medium) rs963596010 Functional Loss DEL dbSNP153 33..35 33 - - - 58466 RMVar_ID_58466 Human_SNP_ID_392209014 m1A Human chr9 - 17503513 17503513 17503513 AAGTTGAGTGCAGAGTATTCTAGAAAGAGAGAAGACCAAGGGCAAATGTGGGAGGCAGGCACCAG AAGTTGAGTGCAGAGTATTCTAGAAAGAGAGAGGACCAAGGGCAAATGTGGGAGGCAGGCACCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:17503468..17503543 26863196 MeRIP-seq:(Medium) rs539026051 Functional Loss SNV dbSNP153 33..33 33 - - - 58467 RMVar_ID_58467 Human_SNP_ID_392233805 m1A Human chr9 + 17579215 17579215 17579215 TCCAGTCCCCCTCCGCCTCCTCCCTCCCGCACAGCAGCCGCCAGCGCGGCCTCCTGCACCATGTC TCCAGTCCCCCTCCGCCTCCTCCCTCCCGCACGGCAGCCGCCAGCGCGGCCTCCTGCACCATGTC A G SH3GL2 Ensembl:ENSG00000107295 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:17579084..17579217 26863196 MeRIP-seq:(Medium) rs1048808558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1034185,Human_Splice_Rec_1034201 58468 RMVar_ID_58468 Human_SNP_ID_392241147 m1A Human chr9 + 17603437 17603437 17603437 GATCCCACTTATAAGGTACCTAGAGTAGTCAAATTCATAGACAGAAAGTAGAACAGTGGTTGAGA GATCCCACTTATAAGGTACCTAGAGTAGTCAAGTTCATAGACAGAAAGTAGAACAGTGGTTGAGA A G SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:17603433..17603546 26863196 MeRIP-seq:(Medium) rs114166533 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6853,GWAS_ID_6854 58469 RMVar_ID_58469 Human_SNP_ID_392469209 m1A Human chr9 + 18336654 18336654 18336654 TTTTTATAGATGGGTGAAGTGGAAGGTTACAAAAAGTAAAAGGAACTCGGCAACTCTTGCCCTGC TTTTTATAGATGGGTGAAGTGGAAGGTTACAATAAGTAAAAGGAACTCGGCAACTCTTGCCCTGC A T ADAMTSL1 Ensembl:ENSG00000178031 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:18336643..18336778 26863196 MeRIP-seq:(Medium) rs1210560288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17201909 RMVar_hsa_circ_255894,RMVar_hsa_circ_255895,RMVar_hsa_circ_255896 58470 RMVar_ID_58470 Human_SNP_ID_392682472 m1A Human chr9 + 19049477 19049477 19049477 CCACTGACAGCCGCGGGCGCTCCCATCTGAGTAAGAGCCAGCCCGTCCGCGGCCTCTCCAGCCCC CCACTGACAGCCGCGGGCGCTCCCATCTGAGTGAGAGCCAGCCCGTCCGCGGCCTCTCCAGCCCC A G RRAGA Ensembl:ENSG00000155876 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:19049426..19049833 26863196 MeRIP-seq:(Medium) rs1376886963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5023935,Human_RBP_ID_5515964,Human_RBP_ID_27134863,Human_RBP_ID_27374086 58471 RMVar_ID_58471 Human_SNP_ID_392682506 m1A Human chr9 + 19049563 19049563 19049563 CTGCCTGCCCAGCTGCGCGGCGGAGCGGAGCGAGGCGCGGCCTGCGAGTCCCCGGCAGCCCCCGA CTGCCTGCCCAGCTGCGCGGCGGAGCGGAGCGTGGCGCGGCCTGCGAGTCCCCGGCAGCCCCCGA A T RRAGA Ensembl:ENSG00000155876 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr9:19049440..19049845;chr9:19049426..19049850 26863196 MeRIP-seq:(Medium) rs1418255440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035634,Human_RBP_ID_22466310 58472 RMVar_ID_58472 Human_SNP_ID_392682511 m1A Human chr9 - 19049573 19049573 19049573 GAGGGAGGGGTCGGGGGCTGCCGGGGACTCGCAGGCCGCGCCTCGCTCCGCTCCGCCGCGCAGCT GAGGGAGGGGTCGGGGGCTGCCGGGGACTCGCCGGCCGCGCCTCGCTCCGCTCCGCCGCGCAGCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:19049526..19049575 26863196 MeRIP-seq:(Medium) rs531335718 Functional Loss SNV dbSNP153 33..33 33 - - - 58473 RMVar_ID_58473 Human_SNP_ID_392700273 m1A Human chr9 + 19102841 19102841 19102841 GGCCTCACAACCTCCGGGAAATTGAGTTTCTAACGGTATAGTGCGGCCACCACTGCCTCAGCGAA GGCCTCACAACCTCCGGGAAATTGAGTTTCTAGCGGTATAGTGCGGCCACCACTGCCTCAGCGAA A G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:19102751..19102900 26863410 MeRIP-seq:(Medium) rs1157365624 Functional Loss SNV dbSNP153 33..33 33 - - - 58474 RMVar_ID_58474 Human_SNP_ID_392742213 m1A Human chr9 - 19230543 19230543 19230543 GCGGCGCGTCGCCTAGGAGCTGCCCGCGGCGCAGCCGTCCCAAGACCTGACCGCCATGTTTCTGT GCGGCGCGTCGCCTAGGAGCTGCCCGCGGCGCCGCCGTCCCAAGACCTGACCGCCATGTTTCTGT T G RF00017-4620,RF00017-4565 RNACentral:URS000092122F,RNACentral:URS000096E4F6 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:19230503..19230779 26863196 MeRIP-seq:(Medium) rs79909362 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6855,GWAS_ID_6856,GWAS_ID_6857,GWAS_ID_6858,GWAS_ID_6859,GWAS_ID_6860,GWAS_ID_6861 58475 RMVar_ID_58475 Human_SNP_ID_392742252 m1A Human chr9 + 19230608 19230608 19230608 CCGCACTGTCCGACGGCTCACAGCGCGGAGGCACCCGCGCGGGCCAGCGCTCCGGCCATCGCCCC CCGCACTGTCCGACGGCTCACAGCGCGGAGGCGCCCGCGCGGGCCAGCGCTCCGGCCATCGCCCC A G DENND4C Ensembl:ENSG00000137145 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:19230552..19230773 26863410 MeRIP-seq:(Medium) rs1269207728 Functional Loss SNV dbSNP153 33..33 33 - - - 58476 RMVar_ID_58476 Human_SNP_ID_392742405 m1A Human chr9 + 19230832 19230832 19230832 GTCGGGGCTGCGCTGACAGAGGAGCAGGCAGCAGGTGAGGCTGCGGCGCGGGGCCTTTGGCGGAG GTCGGGGCTGCGCTGACAGAGGAGCAGGCAGCCGGTGAGGCTGCGGCGCGGGGCCTTTGGCGGAG A C DENND4C Ensembl:ENSG00000137145 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:19230830..19230964 26863196 MeRIP-seq:(Medium) rs1021871278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1034595,Human_Splice_Rec_1034657,Human_Splice_Rec_1034717 58477 RMVar_ID_58477 Human_SNP_ID_392742561 m1A Human chr9 + 19231161 19231161 19231161 GCGTACAAGCGCGAGGGGTCTGGGCCCGGGGGACCGCCGGGGCGACGGCCGCTTTGGTGGGGGCC GCGTACAAGCGCGAGGGGTCTGGGCCCGGGGGGCCGCCGGGGCGACGGCCGCTTTGGTGGGGGCC A G DENND4C Ensembl:ENSG00000137145 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:19231156..19231274 26863196 MeRIP-seq:(Medium) rs112293177 Functional Loss SNV dbSNP153 33..33 33 - - - 58478 RMVar_ID_58478 Human_SNP_ID_392742569 m1A Human chr9 - 19231182 19231182 19231182 ATCCTGCTCCCTCCGCACCCCGGCCCCCACCAAAGCGGCCGTCGCCCCGGCGGTCCCCCGGGCCC ATCCTGCTCCCTCCGCACCCCGGCCCCCACCACAGCGGCCGTCGCCCCGGCGGTCCCCCGGGCCC T G RF00017-4620,RF00017-4565 RNACentral:URS000092122F,RNACentral:URS000096E4F6 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:19231174..19231310 26863196 MeRIP-seq:(Medium) rs1564067109 Functional Loss SNV dbSNP153 33..33 33 - - - 58479 RMVar_ID_58479 Human_SNP_ID_392744469 m1A Human chr9 - 19236662 19236662 19236662 ATTTTCTACCCCTACCATGCTGTTCTCAATACATGCCTAGGTGCCTTCAAGATGTTCTGGATGAT ATTTTCTACCCCTACCATGCTGTTCTCAATACCTGCCTAGGTGCCTTCAAGATGTTCTGGATGAT T G RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:19236579..19236708 26863196 MeRIP-seq:(Medium) rs1281073153 Functional Loss SNV dbSNP153 33..33 33 - - - 58480 RMVar_ID_58480 Human_SNP_ID_392789097 m1A Human chr9 - 19376382 19376382 19376382 ACTGTTTGCTGTTTTGTTTTGTTTAGGAGGCTAAGGAGAAGCGCCAGGAACAAATTGCGAAGAGA ACTGTTTGCTGTTTTGTTTTGTTTAGGAGGCTGAGGAGAAGCGCCAGGAACAAATTGCGAAGAGA T C RPS6 Ensembl:ENSG00000137154 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:19376369..19376475 26863196 MeRIP-seq:(Medium) rs759504638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_218259,Human_RBP_ID_256042,Human_RBP_ID_716610,Human_RBP_ID_797552,Human_RBP_ID_846699,Human_RBP_ID_964716,Human_RBP_ID_1058797,Human_RBP_ID_1146227,Human_RBP_ID_1704174,Human_RBP_ID_2062974,Human_RBP_ID_5041909,Human_RBP_ID_7913436,Human_RBP_ID_8701581,Human_RBP_ID_9234884,Human_RBP_ID_9406814,Human_RBP_ID_16634314,Human_RBP_ID_17666463,Human_RBP_ID_18140756,Human_RBP_ID_18907086,Human_RBP_ID_21709661,Human_RBP_ID_22119603,Human_RBP_ID_23141554,Human_RBP_ID_24549796,Human_RBP_ID_27134959 Human_Splice_Rec_1034890,Human_Splice_Rec_1034892,Human_Splice_Rec_1034900,Human_Splice_Rec_1034910 RMVar_hsa_circ_88413,RMVar_hsa_circ_122551,RMVar_hsa_circ_119085,RMVar_hsa_circ_120519,RMVar_hsa_circ_107449,RMVar_hsa_circ_255999,RMVar_hsa_circ_256001,RMVar_hsa_circ_256003,RMVar_hsa_circ_77164,RMVar_hsa_circ_256002,RMVar_hsa_circ_256000,RMVar_hsa_circ_255998 58481 RMVar_ID_58481 Human_SNP_ID_392789098 m1A Human chr9 + 19376383 19376383 19376383 CTCTTCGCAATTTGTTCCTGGCGCTTCTCCTTAGCCTCCTAAACAAAACAAAACAGCAAACAGTT CTCTTCGCAATTTGTTCCTGGCGCTTCTCCTTGGCCTCCTAAACAAAACAAAACAGCAAACAGTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:19376369..19376461 26863196 MeRIP-seq:(Medium) rs1466018356 Functional Loss SNV dbSNP153 33..33 33 - - - 58482 RMVar_ID_58482 Human_SNP_ID_392790063 m1A Human chr9 + 19378859 19378859 19378859 AGTAGCAGGCGGACACGGCCATGGGTCAAGACACCCTGCTTCATGGGGAAACCTTGTTTGTCGTT AGTAGCAGGCGGACACGGCCATGGGTCAAGACGCCCTGCTTCATGGGGAAACCTTGTTTGTCGTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:19378351..19378971 32194978 MeRIP-seq:(Medium) rs772074797 Functional Loss SNV dbSNP153 33..33 33 - - - 58483 RMVar_ID_58483 Human_SNP_ID_392790064 m1A Human chr9 + 19378859 19378859 19378859 AGTAGCAGGCGGACACGGCCATGGGTCAAGACACCCTGCTTCATGGGGAAACCTTGTTTGTCGTT AGTAGCAGGCGGACACGGCCATGGGTCAAGACTCCCTGCTTCATGGGGAAACCTTGTTTGTCGTT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:19378351..19378971 32194978 MeRIP-seq:(Medium) rs772074797 Functional Loss SNV dbSNP153 33..33 33 - - - 58484 RMVar_ID_58484 Human_SNP_ID_392790316 m1A Human chr9 - 19379447 19379446 19379448 TTGACAAATTGTTGCAGGTATTTAAGTCAGAGACGGTAAACGCCATTGGTAACTGGTATTTGGAA TTGACAAATTGTTGCAGGTATTTAAGTCAGA__CGGTAAACGCCATTGGTAACTGGTATTTGGAA GTC G RPS6 Ensembl:ENSG00000137154 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:19379445..19379592;chr9:19379444..19379570 26863196 MeRIP-seq:(Medium) rs764971346 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_91365,Human_RBP_ID_3198844,Human_RBP_ID_16634448,Human_RBP_ID_24296099,Human_RBP_ID_27843580 RMVar_hsa_circ_13482,RMVar_hsa_circ_120519,RMVar_hsa_circ_256003,RMVar_hsa_circ_77164,RMVar_hsa_circ_256002,RMVar_hsa_circ_108329,RMVar_hsa_circ_256008 58485 RMVar_ID_58485 Human_SNP_ID_392790358 m1A Human chr9 - 19379542 19379542 19379542 AGTGGACGATGAACGCAAACTTCGTACTTTCTATGAGAAGCGTATGGCCACAGAAGTTGCTGCTG AGTGGACGATGAACGCAAACTTCGTACTTTCTTTGAGAAGCGTATGGCCACAGAAGTTGCTGCTG T A RPS6 Ensembl:ENSG00000137154 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:19379464..19379625 32194978 MeRIP-seq:(Medium) rs370530821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_716638,Human_RBP_ID_1403019,Human_RBP_ID_1704204,Human_RBP_ID_2062993,Human_RBP_ID_3198845,Human_RBP_ID_3897125,Human_RBP_ID_5024159,Human_RBP_ID_8701606,Human_RBP_ID_9234895,Human_RBP_ID_9314679,Human_RBP_ID_16634452,Human_RBP_ID_17666468,Human_RBP_ID_18133610,Human_RBP_ID_18397583,Human_RBP_ID_18907105,Human_RBP_ID_22117703,Human_RBP_ID_22339109,Human_RBP_ID_22838428,Human_RBP_ID_23091643,Human_RBP_ID_24296100,Human_RBP_ID_26562892,Human_RBP_ID_27134979,Human_RBP_ID_27374186,Human_RBP_ID_27545185 Human_Splice_Rec_1034882,Human_Splice_Rec_1034883,Human_Splice_Rec_1034893,Human_Splice_Rec_1034902,Human_Splice_Rec_1034903,Human_Splice_Rec_1034912 Human_miRNA_ID_2393011,Human_miRNA_ID_2534406,Human_miRNA_ID_2536140 RMVar_hsa_circ_13482,RMVar_hsa_circ_120519,RMVar_hsa_circ_256003,RMVar_hsa_circ_77164,RMVar_hsa_circ_256002,RMVar_hsa_circ_108329,RMVar_hsa_circ_256008 58486 RMVar_ID_58486 Human_SNP_ID_392790359 m1A Human chr9 - 19379542 19379542 19379542 AGTGGACGATGAACGCAAACTTCGTACTTTCTATGAGAAGCGTATGGCCACAGAAGTTGCTGCTG AGTGGACGATGAACGCAAACTTCGTACTTTCTGTGAGAAGCGTATGGCCACAGAAGTTGCTGCTG T C RPS6 Ensembl:ENSG00000137154 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:19379464..19379625 32194978 MeRIP-seq:(Medium) rs370530821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_716638,Human_RBP_ID_1403019,Human_RBP_ID_1704204,Human_RBP_ID_2062993,Human_RBP_ID_3198845,Human_RBP_ID_3897125,Human_RBP_ID_5024159,Human_RBP_ID_8701606,Human_RBP_ID_9234895,Human_RBP_ID_9314679,Human_RBP_ID_16634452,Human_RBP_ID_17666468,Human_RBP_ID_18133610,Human_RBP_ID_18397583,Human_RBP_ID_18907105,Human_RBP_ID_22117703,Human_RBP_ID_22339109,Human_RBP_ID_22838428,Human_RBP_ID_23091643,Human_RBP_ID_24296100,Human_RBP_ID_26562892,Human_RBP_ID_27134979,Human_RBP_ID_27374186,Human_RBP_ID_27545185 Human_Splice_Rec_1034882,Human_Splice_Rec_1034883,Human_Splice_Rec_1034893,Human_Splice_Rec_1034902,Human_Splice_Rec_1034903,Human_Splice_Rec_1034912 Human_miRNA_ID_2393011,Human_miRNA_ID_2534406,Human_miRNA_ID_2536140 RMVar_hsa_circ_13482,RMVar_hsa_circ_120519,RMVar_hsa_circ_256003,RMVar_hsa_circ_77164,RMVar_hsa_circ_256002,RMVar_hsa_circ_108329,RMVar_hsa_circ_256008 58487 RMVar_ID_58487 Human_SNP_ID_392790557 m1A Human chr9 - 19380016 19380016 19380016 GGGGCATGGAGCTTTTTGGCCGAACGGATGGCAGGCGATTGCGGCTGGAGCCGCGGCGGGCCGGG GGGGCATGGAGCTTTTTGGCCGAACGGATGGCGGGCGATTGCGGCTGGAGCCGCGGCGGGCCGGG T C RPS6 Ensembl:ENSG00000137154 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:19380013..19380250 26863196 MeRIP-seq:(Medium) rs1364861692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16634480,Human_RBP_ID_17175099,Human_RBP_ID_22118654,Human_RBP_ID_24296112 RMVar_hsa_circ_13482,RMVar_hsa_circ_120519,RMVar_hsa_circ_256003 58488 RMVar_ID_58488 Human_SNP_ID_392811846 m1A Human chr9 + 19445858 19445858 19445858 GGCTGTAGGGGCAAGGGTGGAAGGAGACTCTGATGAGATGGCGGTAGCATGGATCTAGATGGAGG GGCTGTAGGGGCAAGGGTGGAAGGAGACTCTGCTGAGATGGCGGTAGCATGGATCTAGATGGAGG A C ACER2 Ensembl:ENSG00000177076 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:19445810..19445936 26863196 MeRIP-seq:(Medium) rs143741778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89379,RMVar_hsa_circ_373471,RMVar_hsa_circ_256013,RMVar_hsa_circ_256014 58489 RMVar_ID_58489 Human_SNP_ID_392811847 m1A Human chr9 + 19445858 19445858 19445858 GGCTGTAGGGGCAAGGGTGGAAGGAGACTCTGATGAGATGGCGGTAGCATGGATCTAGATGGAGG GGCTGTAGGGGCAAGGGTGGAAGGAGACTCTGTTGAGATGGCGGTAGCATGGATCTAGATGGAGG A T ACER2 Ensembl:ENSG00000177076 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:19445810..19445936 26863196 MeRIP-seq:(Medium) rs143741778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89379,RMVar_hsa_circ_373471,RMVar_hsa_circ_256013,RMVar_hsa_circ_256014 58490 RMVar_ID_58490 Human_SNP_ID_393096402 m1A Human chr9 - 20363557 20363557 20363557 AATGAAAGATCTGCATTCTGATGACAATGAGGAGGAATCAGATGAAGTGGAGGATAACGACAATG AATGAAAGATCTGCATTCTGATGACAATGAGGGGGAATCAGATGAAGTGGAGGATAACGACAATG T C MLLT3 Ensembl:ENSG00000171843 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:20363426..20363625 26863196 MeRIP-seq:(Medium) rs1346134565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2063013 Human_Splice_Rec_1034978,Human_Splice_Rec_1034979,Human_Splice_Rec_1034998,Human_Splice_Rec_1034999,Human_Splice_Rec_1035008,Human_Splice_Rec_1035009,Human_Splice_Rec_1035026,Human_Splice_Rec_1035027,Human_Splice_Rec_1035035,Human_Splice_Rec_1035048,Human_Splice_Rec_1035049,Human_Splice_Rec_1035062,Human_Splice_Rec_1035063,Human_Splice_Rec_1035070,Human_Splice_Rec_1035071,Human_Splice_Rec_1035080 RMVar_hsa_circ_330332,RMVar_hsa_circ_256022,RMVar_hsa_circ_256028,RMVar_hsa_circ_290422,RMVar_hsa_circ_256027,RMVar_hsa_circ_256031,RMVar_hsa_circ_256030,RMVar_hsa_circ_269080,RMVar_hsa_circ_276382,RMVar_hsa_circ_374478,RMVar_hsa_circ_256029,RMVar_hsa_circ_376215 58491 RMVar_ID_58491 Human_SNP_ID_393096984 m1A Human chr9 + 20365695 20365695 20365695 TGATACCTTGTTGCCTGGTCTGGGATGGTGTGAAGCTGGAGCTGGAGCTGGAGCTGGAGCTGGCA TGATACCTTGTTGCCTGGTCTGGGATGGTGTGGAGCTGGAGCTGGAGCTGGAGCTGGAGCTGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:20363584..20380209 26863196 MeRIP-seq:(Medium) rs1563938129 Functional Loss SNV dbSNP153 33..33 33 - - - 58492 RMVar_ID_58492 Human_SNP_ID_393109419 m1A Human chr9 + 20414312 20414282 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTG______________________________CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTGCTGCTGCTGCTGCTACTGCTGCTGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs1554680642 Functional Loss DEL dbSNP153 4..33 33 - - - 58493 RMVar_ID_58493 Human_SNP_ID_393109421 m1A Human chr9 + 20414312 20414285 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTG___________________________CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTGCTGCTGCTGCTACTGCTGCTGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs1257565231 Functional Loss DEL dbSNP153 7..33 33 - - - 58494 RMVar_ID_58494 Human_SNP_ID_393109430 m1A Human chr9 - 20414296 20414294 20414296 GCAGCAGCAGCAGCAGTAGCAGCAGCAGTAGCAGCAGCAGCAGCAGCAGTAGTACCAGTTTTTCA GCAGCAGCAGCAGCAGTAGCAGCAGCAGTAGC__CAGCAGCAGCAGCAGTAGTACCAGTTTTTCA GCT G MLLT3 Ensembl:ENSG00000171843 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:20414258..20414347 26863196 MeRIP-seq:(Medium) rs1203032867 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_256036,RMVar_hsa_circ_291964,RMVar_hsa_circ_256032,RMVar_hsa_circ_316325,RMVar_hsa_circ_282522,RMVar_hsa_circ_256034,RMVar_hsa_circ_256035,RMVar_hsa_circ_256033 58495 RMVar_ID_58495 Human_SNP_ID_393109435 m1A Human chr9 + 20414312 20414297 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTG_______________CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTACTGCTGCTGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs756056977 Functional Loss DEL dbSNP153 19..33 33 - - - 58496 RMVar_ID_58496 Human_SNP_ID_393109446 m1A Human chr9 - 20414335 20414300 20414378 GCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGC GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC ACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTA GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG MLLT3 Ensembl:ENSG00000171843 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:20414285..20414363 26863196 MeRIP-seq:(Medium) rs1554680672 Functional Loss MNV dbSNP153 1..65 33 - - - Human_Splice_Rec_1034974,Human_Splice_Rec_1034994,Human_Splice_Rec_1035022,Human_Splice_Rec_1035076 RMVar_hsa_circ_256036,RMVar_hsa_circ_291964,RMVar_hsa_circ_256032,RMVar_hsa_circ_316325,RMVar_hsa_circ_282522,RMVar_hsa_circ_256034,RMVar_hsa_circ_256035,RMVar_hsa_circ_256033 58497 RMVar_ID_58497 Human_SNP_ID_393109446 m1A Human chr9 + 20414312 20414300 20414378 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT ACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTA GCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs1554680672 Functional Loss MNV dbSNP153 21..65 33 - - - 58498 RMVar_ID_58498 Human_SNP_ID_393109453 m1A Human chr9 + 20414312 20414303 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTG_________CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTGCTGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs780013387 Functional Loss DEL dbSNP153 25..33 33 - - - 58499 RMVar_ID_58499 Human_SNP_ID_393109457 m1A Human chr9 + 20414312 20414306 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTGCTG______CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs1179028638 Functional Loss DEL dbSNP153 28..33 33 - - - 58500 RMVar_ID_58500 Human_SNP_ID_393109459 m1A Human chr9 + 20414312 20414308 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTGCTGCT____CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT TGCTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs772288806 Functional Loss DEL dbSNP153 30..33 33 - - - 58501 RMVar_ID_58501 Human_SNP_ID_393109461 m1A Human chr9 + 20414312 20414309 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTGCTGCTG___CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT GCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs773355057 Functional Loss DEL dbSNP153,HGVD 31..33 33 - - - 58502 RMVar_ID_58502 Human_SNP_ID_393109464 m1A Human chr9 + 20414312 20414312 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs148318848 Functional Loss SNV dbSNP153 33..33 33 - - - 58503 RMVar_ID_58503 Human_SNP_ID_393109497 m1A Human chr9 - 20414335 20414335 20414335 GCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGC GCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGCTGCAGCAGCAGCAGCAGCAGCAGTAGCAGCAGC T A MLLT3 Ensembl:ENSG00000171843 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:20414285..20414363 26863196 MeRIP-seq:(Medium) rs1306612727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1034974,Human_Splice_Rec_1034994,Human_Splice_Rec_1035022,Human_Splice_Rec_1035076 RMVar_hsa_circ_256036,RMVar_hsa_circ_291964,RMVar_hsa_circ_256032,RMVar_hsa_circ_316325,RMVar_hsa_circ_282522,RMVar_hsa_circ_256034,RMVar_hsa_circ_256035,RMVar_hsa_circ_256033 58504 RMVar_ID_58504 Human_SNP_ID_393167538 m1A Human chr9 - 20622391 20622391 20622391 GCGAGCAAGCGAGCGCGGGGGGAAAAAGGCAGAGAATGTCCGCCATCTACCCTCCGCTCCTGGGC GCGAGCAAGCGAGCGCGGGGGGAAAAAGGCAGGGAATGTCCGCCATCTACCCTCCGCTCCTGGGC T C MLLT3 Ensembl:ENSG00000171843 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:20622340..20622493 26863196 MeRIP-seq:(Medium) rs1470108954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22838442,Human_RBP_ID_23091766,Human_RBP_ID_26242719 58505 RMVar_ID_58505 Human_SNP_ID_393178218 m1A Human chr9 + 20658417 20658417 20658417 CGCCTTGCAGGTTGATCTCAGACTGCTGTGCTAGCAATCAGTGAGACTCCGTGGGCGTAGGACTC CGCCTTGCAGGTTGATCTCAGACTGCTGTGCTGGCAATCAGTGAGACTCCGTGGGCGTAGGACTC A G FOCAD Ensembl:ENSG00000188352 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20658366..20658478 26863196 MeRIP-seq:(Medium) rs922994892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1035081 58506 RMVar_ID_58506 Human_SNP_ID_393179170 m1A Human chr9 + 20660891 20660891 20660891 AGGATATGAGAGGCAGACAGTCAAAGAGAAAGAGAGAGAGAGAGAGCAATTTGGGCAAAAATTAT AGGATATGAGAGGCAGACAGTCAAAGAGAAAGGGAGAGAGAGAGAGCAATTTGGGCAAAAATTAT A G FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20660784..20661064 26863196 MeRIP-seq:(Medium) rs1435090713 Functional Loss SNV dbSNP153 33..33 33 - - - 58507 RMVar_ID_58507 Human_SNP_ID_393185718 m1A Human chr9 - 20684317 20684317 20684317 CGGCGGCTCCCGAGCAGGGGTGCAGCGGTGGCAGCCCGCCGCCCCGCACGGCTTACCTCCCTTCT CGGCGGCTCCCGAGCAGGGGTGCAGCGGTGGCCGCCCGCCGCCCCGCACGGCTTACCTCCCTTCT T G FOCAD-AS1 Ensembl:ENSG00000227071 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20684293..20684467 26863196 MeRIP-seq:(Medium) rs1370644385 Functional Loss SNV dbSNP153 33..33 33 - - - 58508 RMVar_ID_58508 Human_SNP_ID_393185726 m1A Human chr9 + 20684329 20684329 20684329 AGCCGTGCGGGGCGGCGGGCTGCCACCGCTGCACCCCTGCTCGGGAGCCGCCGGGTCGCGCCGCC AGCCGTGCGGGGCGGCGGGCTGCCACCGCTGCGCCCCTGCTCGGGAGCCGCCGGGTCGCGCCGCC A G FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:20684324..20684471 26863196 MeRIP-seq:(Medium) rs1266053990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18427137,Human_RBP_ID_21995794 58509 RMVar_ID_58509 Human_SNP_ID_393379065 m1A Human chr9 + 21324198 21324198 21324198 CAGTTGTCTGAAGGTTCTGTTTGGGCTGGCGGATCTGTTTCTAACATGGGTCACTCACACGGCCA CAGTTGTCTGAAGGTTCTGTTTGGGCTGGCGGGTCTGTTTCTAACATGGGTCACTCACACGGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:21324151..21324231 26863196 MeRIP-seq:(Medium) rs1268730073 Functional Loss SNV dbSNP153 33..33 33 - - - 58510 RMVar_ID_58510 Human_SNP_ID_393432606 m1A Human chr9 + 21519546 21519546 21519546 CCCTCAGAGTCTGCATTCTATCTGTGCCCCCAAACTAACTTCCAACATTACCACCCTTATTTTCT CCCTCAGAGTCTGCATTCTATCTGTGCCCCCACACTAACTTCCAACATTACCACCCTTATTTTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:21519544..21519626 26863196 MeRIP-seq:(Medium) rs556403851 Functional Loss SNV dbSNP153 33..33 33 - - - 58511 RMVar_ID_58511 Human_SNP_ID_393432607 m1A Human chr9 + 21519547 21519547 21519547 CCTCAGAGTCTGCATTCTATCTGTGCCCCCAAACTAACTTCCAACATTACCACCCTTATTTTCTA CCTCAGAGTCTGCATTCTATCTGTGCCCCCAAGCTAACTTCCAACATTACCACCCTTATTTTCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21519540..21519648 26863196 MeRIP-seq:(Medium) rs987663084 Functional Loss SNV dbSNP153 33..33 33 - - - 58512 RMVar_ID_58512 Human_SNP_ID_393443880 m1A Human chr9 + 21559261 21559261 21559261 CCAGGATGACGACCTGAGATTTGGACAAGAGGAGGCGGCGGTTCCGCGAAGAGCCAAGGGCGGCC CCAGGATGACGACCTGAGATTTGGACAAGAGGGGGCGGCGGTTCCGCGAAGAGCCAAGGGCGGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:21559181..21559294 32194978 MeRIP-seq:(Medium) rs1304718982 Functional Loss SNV dbSNP153 33..33 33 - - - 58513 RMVar_ID_58513 Human_SNP_ID_393444012 m1A Human chr9 + 21559569 21559569 21559569 CGCACACGAAGGGGCCGCTTCCCGCCCCCCGCACCCCAGACCAGGCGGCTCACGGAACACCGCCT CGCACACGAAGGGGCCGCTTCCCGCCCCCCGCCCCCCAGACCAGGCGGCTCACGGAACACCGCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21559519..21559795 26863196 MeRIP-seq:(Medium) rs902925858 Functional Loss SNV dbSNP153 33..33 33 - - - 58514 RMVar_ID_58514 Human_SNP_ID_393444063 m1A Human chr9 - 21559708 21559708 21559708 GCTGCGACCTGTGCATAACTTGGGGCGCCGCCAGGGGCTCGCAGGTTCCACGTCCGGCGCCTGGA GCTGCGACCTGTGCATAACTTGGGGCGCCGCCCGGGGCTCGCAGGTTCCACGTCCGGCGCCTGGA T G MIR31HG Ensembl:ENSG00000171889 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21559667..21559766 26863196 MeRIP-seq:(Medium) rs1444991028 Functional Loss SNV dbSNP153 33..33 33 - - - 58515 RMVar_ID_58515 Human_SNP_ID_393524365 m1A Human chr9 + 21806175 21806175 21806175 TGTTGTATACAGAATAGCCTGTGGGCAGGGGAAGAGCTAAGAGATCAGGCCAGAAGTCTTGGTGC TGTTGTATACAGAATAGCCTGTGGGCAGGGGAGGAGCTAAGAGATCAGGCCAGAAGTCTTGGTGC A G AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:21806173..21806285 26863196 MeRIP-seq:(Medium) rs538351229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256177,RMVar_hsa_circ_127908 58516 RMVar_ID_58516 Human_SNP_ID_393551026 m1A Human chr9 + 21899476 21899476 21899476 GGAAAGGAAGGAAGGAAAAGAAAGAACTGCCCAAGATTGGGTAATTTATAAAGGAGAGAGGTTCA GGAAAGGAAGGAAGGAAAAGAAAGAACTGCCCGAGATTGGGTAATTTATAAAGGAGAGAGGTTCA A G AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21899445..21899618 26863196 MeRIP-seq:(Medium) rs200036590 Functional Loss SNV dbSNP153 33..33 33 - - - 58517 RMVar_ID_58517 Human_SNP_ID_393569910 m1A Human chr9 + 21968239 21968239 21968239 TCTCAGAGCCTCTCTGGTTCTTTCAATCGGGGATGTCTGCAGAGGGCAGAAAGAAAACAGGCGTT TCTCAGAGCCTCTCTGGTTCTTTCAATCGGGGTTGTCTGCAGAGGGCAGAAAGAAAACAGGCGTT A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr9:21968078..21968285;chr9:21968026..21968267;chr9:21968026..21968280;chr9:21968026..21968289;chr9:21968151..21968250 26863196,32194978 MeRIP-seq:(Medium) rs1554653284 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_177 58518 RMVar_ID_58518 Human_SNP_ID_393570744 m1A Human chr9 + 21970974 21970974 21970974 GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTACCGTGCGACATCGCGATGGCCCAGCTCCTCAG GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTCCCGTGCGACATCGCGATGGCCCAGCTCCTCAG A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970951..21970975 26863196 MeRIP-seq:(Medium) rs1554653923 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_178 58519 RMVar_ID_58519 Human_SNP_ID_393570827 m1A Human chr9 + 21971042 21971042 21971042 GGTCCACGGGCAGACGGCCCCAGGCATCGCGCACGTCCAGCCGCGCCCCGGCCCGGTGCAGCACC GGTCCACGGGCAGACGGCCCCAGGCATCGCGCGCGTCCAGCCGCGCCCCGGCCCGGTGCAGCACC A G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:21970901..21971278 26863410 MeRIP-seq:(Medium) rs1554654028 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_179 58520 RMVar_ID_58520 Human_SNP_ID_393570899 m1A Human chr9 - 21971111 21971111 21971111 CGCCGACCCCGCCACTCTCACCCGACCCGTGCACGACGCTGCCCGGGAGGGCTTCCTGGACACGC CGCCGACCCCGCCACTCTCACCCGACCCGTGCGCGACGCTGCCCGGGAGGGCTTCCTGGACACGC T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:21970877..21971278;chr9:21970868..21971254 26863196 MeRIP-seq:(Medium) rs1057519881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717038,Human_RBP_ID_8275220,Human_RBP_ID_18134011,Human_RBP_ID_18212440,Human_RBP_ID_24297451,Human_RBP_ID_27545288 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1549725,Human_miRNA_ID_1549902,Human_miRNA_ID_1550232 Clinvar_Rec_180 58521 RMVar_ID_58521 Human_SNP_ID_393570970 m1A Human chr9 - 21971162 21971162 21971162 CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAACTGCGCCGACCCCGCCA CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCGCGGCGCGGAGCCCAACTGCGCCGACCCCGCCA T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970995..21971204 26863196 MeRIP-seq:(Medium) rs756750256 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_717039,Human_RBP_ID_5042037,Human_RBP_ID_8702224,Human_RBP_ID_18134013,Human_RBP_ID_24297452,Human_RBP_ID_24523182,Human_RBP_ID_27135409,Human_RBP_ID_27374365 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Clinvar_Rec_181,Clinvar_Rec_182 58522 RMVar_ID_58522 Human_SNP_ID_393570971 m1A Human chr9 - 21971162 21971162 21971162 CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAACTGCGCCGACCCCGCCA CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCCCGGCGCGGAGCCCAACTGCGCCGACCCCGCCA T G CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970995..21971204 26863196 MeRIP-seq:(Medium) rs756750256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717039,Human_RBP_ID_5042037,Human_RBP_ID_8702224,Human_RBP_ID_18134013,Human_RBP_ID_24297452,Human_RBP_ID_24523182,Human_RBP_ID_27135409,Human_RBP_ID_27374365 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Clinvar_Rec_181,Clinvar_Rec_182 58523 RMVar_ID_58523 Human_SNP_ID_393571012 m1A Human chr9 + 21971204 21971204 21971204 GCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGC GCAGCTCCGCCACTCGGGCGCTGCCCATCATCGTGACCTGCCAGAGAGAACAGAATGGTCAGAGC A G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21970862..21971254 26863196 MeRIP-seq:(Medium) rs752573958 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_183 58524 RMVar_ID_58524 Human_SNP_ID_393572106 m1A Human chr9 + 21974759 21974758 21974759 GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GCCTCCAGCAGCGCCCGCACCTCCTCTACCCG_CCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GA G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:21974676..21975075 26863196 MeRIP-seq:(Medium) rs1563892715 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_184 58525 RMVar_ID_58525 Human_SNP_ID_393572107 m1A Human chr9 + 21974759 21974759 21974759 GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGCCCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:21974676..21975075 26863196 MeRIP-seq:(Medium) rs766772030 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_185 58526 RMVar_ID_58526 Human_SNP_ID_393572134 m1A Human chr9 + 21974781 21974777 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTG____GCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC GGCCA G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs587782206 Functional Loss DEL dbSNP153 30..33 33 - - - Clinvar_Rec_186 58527 RMVar_ID_58527 Human_SNP_ID_393572140 m1A Human chr9 + 21974781 21974781 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCCGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs864622263 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_187,Clinvar_Rec_188 58528 RMVar_ID_58528 Human_SNP_ID_393572141 m1A Human chr9 + 21974781 21974781 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCTGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs864622263 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_187,Clinvar_Rec_188 58529 RMVar_ID_58529 Human_SNP_ID_393572149 m1A Human chr9 + 21974789 21974789 21974789 CGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCCGCCGCCGG CGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCCGCCGAAGGCTCCATGCTGCTCCCCGCCGCCGG A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr9:21974726..21974878 26863410 MeRIP-seq:(Medium) rs786201931 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_189,Clinvar_Rec_13687 58530 RMVar_ID_58530 Human_SNP_ID_393572172 m1A Human chr9 - 21974809 21974809 21974809 CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCC CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGGTGCAGCATGGAGCCTTCGGCTGACTGGCTGGCC T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:21974720..21974890 26863410 MeRIP-seq:(Medium) rs1554656670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92522,Human_RBP_ID_5024668 Clinvar_Rec_190 58531 RMVar_ID_58531 Human_SNP_ID_393576113 m1A Human chr9 - 21989601 21989601 21989601 GTGAGTCAGGGTTACCCGGAGGAACCACGGGGAAAGTGCGCTTCTGAGACTCTTGACAGCCATTT GTGAGTCAGGGTTACCCGGAGGAACCACGGGGCAAGTGCGCTTCTGAGACTCTTGACAGCCATTT T G CDKN2A Ensembl:ENSG00000147889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21989600..21989768 26863196 MeRIP-seq:(Medium) rs1421519935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3203277,Human_RBP_ID_7916729,Human_RBP_ID_16644127 58532 RMVar_ID_58532 Human_SNP_ID_393577379 m1A Human chr9 - 21994227 21994217 21994227 GTTCACATCCCGCGGCTCACGGGGGAGTGGGCAGCGCCAGGGGCGCCCGCCGCTGTGGCCCTCGT GTTCACATCCCGCGGCTCACGGGGGAGTGGGC__________GCGCCCGCCGCTGTGGCCCTCGT CCCCTGGCGCT C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr9:21994176..21994400;chr9:21994176..21994853 26863196 MeRIP-seq:(Medium) rs768804955 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_92524,Human_RBP_ID_256694,Human_RBP_ID_717061,Human_RBP_ID_5024706,Human_RBP_ID_22339396,Human_RBP_ID_22838468,Human_RBP_ID_24523189 Human_Splice_Rec_1035553,Human_Splice_Rec_1035563 58533 RMVar_ID_58533 Human_SNP_ID_393577408 m1A Human chr9 - 21994253 21994253 21994253 GCCCGCCGCGAGTGAGGGTTTTCGTGGTTCACATCCCGCGGCTCACGGGGGAGTGGGCAGCGCCA GCCCGCCGCGAGTGAGGGTTTTCGTGGTTCACCTCCCGCGGCTCACGGGGGAGTGGGCAGCGCCA T G CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:21994203..21994400 26863196 MeRIP-seq:(Medium) rs1057517575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92524,Human_RBP_ID_256694,Human_RBP_ID_717061,Human_RBP_ID_1058874,Human_RBP_ID_5024706,Human_RBP_ID_5482625,Human_RBP_ID_18907509,Human_RBP_ID_24297531 Clinvar_Rec_191 58534 RMVar_ID_58534 Human_SNP_ID_393577450 m1A Human chr9 - 21994333 21994333 21994333 GGCTGCCGAGCTCGGCCCTGGAGGCGGCGAGAACATGGTGCGCAGGTTCTTGGTGACCCTCCGGA GGCTGCCGAGCTCGGCCCTGGAGGCGGCGAGATCATGGTGCGCAGGTTCTTGGTGACCCTCCGGA T A CDKN2A Ensembl:ENSG00000147889 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21994112..21994853 26863196 MeRIP-seq:(Medium) rs764949869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717067,Human_RBP_ID_1704457,Human_RBP_ID_5024707,Human_RBP_ID_24297533 58535 RMVar_ID_58535 Human_SNP_ID_393577606 m1A Human chr9 + 21994610 21994610 21994610 CGCACGCGGGAAGGGCTGCCGGAGGCGCCCGTAGGGAGGCGCGCGCGCGGGCGGCTCAGGGCCCG CGCACGCGGGAAGGGCTGCCGGAGGCGCCCGTTGGGAGGCGCGCGCGCGGGCGGCTCAGGGCCCG A T AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:21994607..21994977 26863196 MeRIP-seq:(Medium) rs1563903506 Functional Loss SNV dbSNP153 33..33 33 - - - 58536 RMVar_ID_58536 Human_SNP_ID_393580476 m1A Human chr9 + 22005953 22005953 22005953 AGGTGGGTGGGGGTGGGAAATTGGGTAAGAAAATAAAGTCGTTGTGGGCGGCTGGGGAACCTGGC AGGTGGGTGGGGGTGGGAAATTGGGTAAGAAAGTAAAGTCGTTGTGGGCGGCTGGGGAACCTGGC A G AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:22005920..22006069 32194978 MeRIP-seq:(Medium) rs768447646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256182,RMVar_hsa_circ_111947 58537 RMVar_ID_58537 Human_SNP_ID_393581330 m1A Human chr9 - 22008799 22008799 22008799 CGGAGTCAACCGTTTCGGGAGGCGCGCGATCCAGGTAGCTGGGGCCCCAGGGCCTCGCCGGCAGG CGGAGTCAACCGTTTCGGGAGGCGCGCGATCCGGGTAGCTGGGGCCCCAGGGCCTCGCCGGCAGG T C CDKN2B Ensembl:ENSG00000147883 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:22008768..22008918 32194978 MeRIP-seq:(Medium) rs769168016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1035901 58538 RMVar_ID_58538 Human_SNP_ID_393581331 m1A Human chr9 - 22008799 22008799 22008799 CGGAGTCAACCGTTTCGGGAGGCGCGCGATCCAGGTAGCTGGGGCCCCAGGGCCTCGCCGGCAGG CGGAGTCAACCGTTTCGGGAGGCGCGCGATCCCGGTAGCTGGGGCCCCAGGGCCTCGCCGGCAGG T G CDKN2B Ensembl:ENSG00000147883 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:22008768..22008918 32194978 MeRIP-seq:(Medium) rs769168016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1035901 58539 RMVar_ID_58539 Human_SNP_ID_393581439 m1A Human chr9 + 22008984 22008984 22008984 ATTCCGCAGCCCCCAGACGCGCAGCGGCCCGGATAATCCACCGTTGGCCGTAAACTTAACGACAC ATTCCGCAGCCCCCAGACGCGCAGCGGCCCGGTTAATCCACCGTTGGCCGTAAACTTAACGACAC A T AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:22008826..22009300;chr9:22008771..22009300 26863196 MeRIP-seq:(Medium) rs769642333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256182,RMVar_hsa_circ_111947 58540 RMVar_ID_58540 Human_SNP_ID_393584557 m1A Human chr9 + 22018959 22018957 22018960 TGATCTGGTCTGGTGGTTGAGGGAATCAAGAGATATTTGAGTTGAGGTCTGCAGTATTATAGAAA TGATCTGGTCTGGTGGTTGAGGGAATCAAGA___ATTTGAGTTGAGGTCTGCAGTATTATAGAAA AGAT A AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:22018955..22019119 26863196 MeRIP-seq:(Medium) rs562892373 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_256182,RMVar_hsa_circ_111947 58541 RMVar_ID_58541 Human_SNP_ID_393584558 m1A Human chr9 + 22018959 22018959 22018959 TGATCTGGTCTGGTGGTTGAGGGAATCAAGAGATATTTGAGTTGAGGTCTGCAGTATTATAGAAA TGATCTGGTCTGGTGGTTGAGGGAATCAAGAGGTATTTGAGTTGAGGTCTGCAGTATTATAGAAA A G AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:22018955..22019119 26863196 MeRIP-seq:(Medium) rs1040533108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256182,RMVar_hsa_circ_111947 58542 RMVar_ID_58542 Human_SNP_ID_393610968 m1A Human chr9 - 22116612 22116612 22116612 AGTTCTCTGTATTTGCCATTGCTGTTTCCCTCATTTTCATCTCACTGTCTCCTTCTCCTCATTTA AGTTCTCTGTATTTGCCATTGCTGTTTCCCTCGTTTTCATCTCACTGTCTCCTTCTCCTCATTTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:22116565..22116719 26863196 MeRIP-seq:(Medium) rs1374212203 Functional Loss SNV dbSNP153 33..33 33 - - - 58543 RMVar_ID_58543 Human_SNP_ID_393703347 m1A Human chr9 + 22440089 22440086 22440090 AGAGAGAGGAAGCGAGAGAGAAAGAGAAAGAGATAGAAAGTCAAAGAGAAGGAGACAGAAAGGAA AGAGAGAGGAAGCGAGAGAGAAAGAGAAAG____AGAAAGTCAAAGAGAAGGAGACAGAAAGGAA GAGAT G LINC01239 RNACentral:URS0000D58298 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:22439983..22440156 26863196 MeRIP-seq:(Medium) rs979080513 Functional Loss DEL dbSNP153 31..34 33 - - - 58544 RMVar_ID_58544 Human_SNP_ID_394689231 m1A Human chr9 + 25677590 25677590 25677590 GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGAGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGCGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:25677469..25677750 26863196 MeRIP-seq:(Medium) rs10812300 Functional Loss SNV dbSNP153 33..33 33 - - - 58545 RMVar_ID_58545 Human_SNP_ID_394689232 m1A Human chr9 + 25677590 25677590 25677590 GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGAGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGTGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:25677469..25677750 26863196 MeRIP-seq:(Medium) rs10812300 Functional Loss SNV dbSNP153 33..33 33 - - - 58546 RMVar_ID_58546 Human_SNP_ID_394689255 m1A Human chr9 + 25677629 25677629 25677629 CAGGGCGTGCGCGAGGTCGGGGGTAGCTGGGAACGGAGGAGGAGGGGCCCGCTCGAGGCTCCGCC CAGGGCGTGCGCGAGGTCGGGGGTAGCTGGGAGCGGAGGAGGAGGGGCCCGCTCGAGGCTCCGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:25677526..25678038 26863196 MeRIP-seq:(Medium) rs991158461 Functional Loss SNV dbSNP153 33..33 33 - - - 58547 RMVar_ID_58547 Human_SNP_ID_394689256 m1A Human chr9 + 25677629 25677629 25677629 CAGGGCGTGCGCGAGGTCGGGGGTAGCTGGGAACGGAGGAGGAGGGGCCCGCTCGAGGCTCCGCC CAGGGCGTGCGCGAGGTCGGGGGTAGCTGGGATCGGAGGAGGAGGGGCCCGCTCGAGGCTCCGCC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:25677526..25678038 26863196 MeRIP-seq:(Medium) rs991158461 Functional Loss SNV dbSNP153 33..33 33 - - - 58548 RMVar_ID_58548 Human_SNP_ID_394689269 m1A Human chr9 - 25677649 25677649 25677649 CGAGGCCGCAGCCGGTGAGAGGCGGAGCCTCGAGCGGGCCCCTCCTCCTCCGTTCCCAGCTACCC CGAGGCCGCAGCCGGTGAGAGGCGGAGCCTCGCGCGGGCCCCTCCTCCTCCGTTCCCAGCTACCC T G TUSC1 Ensembl:ENSG00000198680 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:25677462..25677805 26863410 MeRIP-seq:(Medium) rs80023951 Functional Loss SNV dbSNP153 33..33 33 - - - 58549 RMVar_ID_58549 Human_SNP_ID_394689557 m1A Human chr9 - 25678026 25678026 25678026 GCTGCGTCAGGAGAACGCCCGGCTGCGGCTCGAGAACCGGCGGCTGAAGCGCGAGAACCGCAGCC GCTGCGTCAGGAGAACGCCCGGCTGCGGCTCGTGAACCGGCGGCTGAAGCGCGAGAACCGCAGCC T A TUSC1 Ensembl:ENSG00000198680 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1448274037 Functional Loss SNV dbSNP153 33..33 33 - - - 58550 RMVar_ID_58550 Human_SNP_ID_395032922 m1A Human chr9 - 26892559 26892559 26892559 GCTGCGGGAGCGCCGGGGGCTGCGGGAGCGTCAGCTGCTGTGGGAACGCCAATTTTAGTGGAAGT GCTGCGGGAGCGCCGGGGGCTGCGGGAGCGTCGGCTGCTGTGGGAACGCCAATTTTAGTGGAAGT T C CAAP1 Ensembl:ENSG00000120159 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:26892457..26892755 26863410 MeRIP-seq:(Medium) rs746643059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036681 58551 RMVar_ID_58551 Human_SNP_ID_395032955 m1A Human chr9 - 26892629 26892629 26892629 GCGGCCGCAGCGCTCGCGGCCCCGGACATCGTACCCGCGTTGGCCAGCGGCAGCAGTGGAAGCAC GCGGCCGCAGCGCTCGCGGCCCCGGACATCGTTCCCGCGTTGGCCAGCGGCAGCAGTGGAAGCAC T A CAAP1 Ensembl:ENSG00000120159 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:26892580..26892743 26863196 MeRIP-seq:(Medium) rs753900549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9235595,Human_RBP_ID_27374448,Human_RBP_ID_27570540 58552 RMVar_ID_58552 Human_SNP_ID_395048500 m1A Human chr9 - 26947186 26947186 26947186 CTCGGCGCGCCCCTTCCCAGCCGCCCTTCCGTACCGGCTCTCGGGCTCTTCCGGTCTCCGGCCGC CTCGGCGCGCCCCTTCCCAGCCGCCCTTCCGTGCCGGCTCTCGGGCTCTTCCGGTCTCCGGCCGC T C PLAA Ensembl:ENSG00000137055 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:26947087..26947340 26863410 MeRIP-seq:(Medium) rs967644773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184768,Human_RBP_ID_717263 58553 RMVar_ID_58553 Human_SNP_ID_395172525 m1A Human chr9 - 27388740 27388740 27388740 AGATGGGGGAGATTGAAGGCAGGAACATGCTTAGAAGGGAAAGGAAAAGAATATATTCAACATGT AGATGGGGGAGATTGAAGGCAGGAACATGCTTTGAAGGGAAAGGAAAAGAATATATTCAACATGT T A MOB3B Ensembl:ENSG00000120162 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:27388738..27388925 26863196 MeRIP-seq:(Medium) rs1222969956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339399 58554 RMVar_ID_58554 Human_SNP_ID_395172534 m1A Human chr9 - 27388784 27388784 27388784 TGGGTTTCTGGCTTGAGAAAGGGAGATGGCCAAGGCACGTACTGAGATGGGGGAGATTGAAGGCA TGGGTTTCTGGCTTGAGAAAGGGAGATGGCCAGGGCACGTACTGAGATGGGGGAGATTGAAGGCA T C MOB3B Ensembl:ENSG00000120162 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:27388782..27388906 26863196 MeRIP-seq:(Medium) rs1029020544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339399 58555 RMVar_ID_58555 Human_SNP_ID_395175315 m1A Human chr9 + 27400332 27400332 27400332 CTCAACCTACCCTTATTCCTGCCATTCACCCAATGCACCCACTTTTCCCCATTGCGGTGACCTCC CTCAACCTACCCTTATTCCTGCCATTCACCCAGTGCACCCACTTTTCCCCATTGCGGTGACCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:27400330..27400440 26863196 MeRIP-seq:(Medium) rs1384315066 Functional Loss SNV dbSNP153 33..33 33 - - - 58556 RMVar_ID_58556 Human_SNP_ID_395653768 m1A Human chr9 + 29188490 29188490 29188490 TTTCCCCACCTTTCCCGCCTTTCTATTCCACGAAACCGCCCCGATTTCTCAATCTTTTCCCCACC TTTCCCCACCTTTCCCGCCTTTCTATTCCACGCAACCGCCCCGATTTCTCAATCTTTTCCCCACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:29188411..29188498 26863196 MeRIP-seq:(Medium) rs1266271127 Functional Loss SNV dbSNP153 33..33 33 - - - 58557 RMVar_ID_58557 Human_SNP_ID_395660360 m1A Human chr9 - 29213479 29213479 29213479 CCTCACCTGGCGCCGCCGCCCGCCGCCCGCCCAGCCCCGCACCGGCGCTGCCTCCCCTGAAAGTT CCTCACCTGGCGCCGCCGCCCGCCGCCCGCCCGGCCCCGCACCGGCGCTGCCTCCCCTGAAAGTT T C lnc-LINGO2-2 RNACentral:URS00008B65F1 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:29213360..29213487 26863196 MeRIP-seq:(Medium) rs1434714483 Functional Loss SNV dbSNP153 33..33 33 - - - 58558 RMVar_ID_58558 Human_SNP_ID_264112606 m1A Human chr6 + 292156 292156 292156 CGGCGGCCGCGAGCCGGGGTCCGCGAGGGCGGAGTGGGGCGCGGCAGCCAGGAACCCGACTACGA CGGCGGCCGCGAGCCGGGGTCCGCGAGGGCGGGGTGGGGCGCGGCAGCCAGGAACCCGACTACGA A G DUSP22 Ensembl:ENSG00000112679 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:292105..292216 26863196 MeRIP-seq:(Medium) rs1433107234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4878243,Human_RBP_ID_18425339 58559 RMVar_ID_58559 Human_SNP_ID_264112608 m1A Human chr6 - 292158 292158 292158 ATTCGTAGTCGGGTTCCTGGCTGCCGCGCCCCACTCCGCCCTCGCGGACCCCGGCTCGCGGCCGC ATTCGTAGTCGGGTTCCTGGCTGCCGCGCCCCGCTCCGCCCTCGCGGACCCCGGCTCGCGGCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:292107..292250 26863196 MeRIP-seq:(Medium) rs1397244567 Functional Loss SNV dbSNP153 33..33 33 - - - 58560 RMVar_ID_58560 Human_SNP_ID_264135511 m1A Human chr6 - 351101 351101 351101 AGTGCGGCAAGGCTCCCGGGATCCTTACAGGCATCCAAGCGAGGTACAGAAACCTCCACAGCAGT AGTGCGGCAAGGCTCCCGGGATCCTTACAGGCCTCCAAGCGAGGTACAGAAACCTCCACAGCAGT T G lnc-EXOC2-15 RNACentral:URS00008B5090 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:351005..351106 32194978 MeRIP-seq:(Medium) rs976942496 Functional Loss SNV dbSNP153 33..33 33 - - - 58561 RMVar_ID_58561 Human_SNP_ID_264138698 m1A Human chr6 - 358670 358670 358670 TCCGTGCCCACCACCCAGGCCACCCCACACAGACTCTTCCTCGCTGCACTTCTTAAAGCCTGCCT TCCGTGCCCACCACCCAGGCCACCCCACACAGGCTCTTCCTCGCTGCACTTCTTAAAGCCTGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:358643..358708 26863196 MeRIP-seq:(Medium) rs1010004306 Functional Loss SNV dbSNP153 33..33 33 - - - 58562 RMVar_ID_58562 Human_SNP_ID_264183164 m1A Human chr6 - 485826 485826 485826 TAACGGAAAGGCCAGGCTCCGCGTGGACGGCCAACTCCCTGCCCGCTCCTTCAGCAGGTGACTGT TAACGGAAAGGCCAGGCTCCGCGTGGACGGCCGACTCCCTGCCCGCTCCTTCAGCAGGTGACTGT T C EXOC2 Ensembl:ENSG00000112685 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:485780..486378 32194978 MeRIP-seq:(Medium) rs796837286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3026115 RMVar_hsa_circ_92587,RMVar_hsa_circ_102003,RMVar_hsa_circ_236833,RMVar_hsa_circ_236834 58563 RMVar_ID_58563 Human_SNP_ID_264207115 m1A Human chr6 - 572637 572637 572637 AGTATTTTATTCTTTTCCCCCTTAGCGTGGAGATACAAAACTCCCCACAGGGTGGCCTTTGTTGA AGTATTTTATTCTTTTCCCCCTTAGCGTGGAGGTACAAAACTCCCCACAGGGTGGCCTTTGTTGA T C EXOC2 Ensembl:ENSG00000112685 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:572588..592586 32194978 MeRIP-seq:(Medium) rs753808699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9309467,Human_RBP_ID_18079187 Human_Splice_Rec_732756 RMVar_hsa_circ_41281,RMVar_hsa_circ_55826,RMVar_hsa_circ_102003,RMVar_hsa_circ_236834,RMVar_hsa_circ_77053,RMVar_hsa_circ_236840,RMVar_hsa_circ_285295,RMVar_hsa_circ_6820,RMVar_hsa_circ_236836,RMVar_hsa_circ_316091,RMVar_hsa_circ_236837,RMVar_hsa_circ_119454,RMVar_hsa_circ_323684,RMVar_hsa_circ_349621,RMVar_hsa_circ_299755,RMVar_hsa_circ_288241,RMVar_hsa_circ_53068,RMVar_hsa_circ_284225,RMVar_hsa_circ_236841,RMVar_hsa_circ_120841,RMVar_hsa_circ_236838,RMVar_hsa_circ_236839,RMVar_hsa_circ_236849,RMVar_hsa_circ_299191,RMVar_hsa_circ_375807,RMVar_hsa_circ_46551,RMVar_hsa_circ_372533,RMVar_hsa_circ_236848,RMVar_hsa_circ_52101,RMVar_hsa_circ_236858,RMVar_hsa_circ_81930,RMVar_hsa_circ_236852,RMVar_hsa_circ_236853,RMVar_hsa_circ_98963,RMVar_hsa_circ_345568,RMVar_hsa_circ_236854,RMVar_hsa_circ_369328,RMVar_hsa_circ_339929,RMVar_hsa_circ_90299,RMVar_hsa_circ_236855,RMVar_hsa_circ_236856,RMVar_hsa_circ_22652,RMVar_hsa_circ_291055,RMVar_hsa_circ_325229,RMVar_hsa_circ_236857,RMVar_hsa_circ_324410,RMVar_hsa_circ_281845,RMVar_hsa_circ_236859,RMVar_hsa_circ_236860 58564 RMVar_ID_58564 Human_SNP_ID_264215095 m1A Human chr6 - 604315 604315 604315 AAGGTAGAGCGAGTGGCAGGTGAGAAAGGTGAAGGGACAGGGAAGGTTTGACATGTTACATAGGG AAGGTAGAGCGAGTGGCAGGTGAGAAAGGTGAGGGGACAGGGAAGGTTTGACATGTTACATAGGG T C EXOC2 Ensembl:ENSG00000112685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:604271..604403 26863196 MeRIP-seq:(Medium) rs1003592789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102003,RMVar_hsa_circ_236834,RMVar_hsa_circ_77053,RMVar_hsa_circ_236840,RMVar_hsa_circ_6820,RMVar_hsa_circ_236836,RMVar_hsa_circ_236837,RMVar_hsa_circ_119454,RMVar_hsa_circ_323684,RMVar_hsa_circ_349621,RMVar_hsa_circ_299755,RMVar_hsa_circ_53068,RMVar_hsa_circ_284225,RMVar_hsa_circ_120841,RMVar_hsa_circ_236838,RMVar_hsa_circ_236839,RMVar_hsa_circ_236849,RMVar_hsa_circ_375807,RMVar_hsa_circ_46551,RMVar_hsa_circ_372533,RMVar_hsa_circ_52101,RMVar_hsa_circ_20539,RMVar_hsa_circ_81930,RMVar_hsa_circ_236852,RMVar_hsa_circ_236853,RMVar_hsa_circ_98963,RMVar_hsa_circ_339929,RMVar_hsa_circ_90299,RMVar_hsa_circ_236855,RMVar_hsa_circ_236856,RMVar_hsa_circ_22652,RMVar_hsa_circ_291055,RMVar_hsa_circ_236857,RMVar_hsa_circ_324410,RMVar_hsa_circ_236860,RMVar_hsa_circ_16708,RMVar_hsa_circ_330273,RMVar_hsa_circ_103696,RMVar_hsa_circ_236863,RMVar_hsa_circ_14054,RMVar_hsa_circ_236862,RMVar_hsa_circ_236866,RMVar_hsa_circ_302601,RMVar_hsa_circ_352153,RMVar_hsa_circ_373708,RMVar_hsa_circ_329232,RMVar_hsa_circ_287227,RMVar_hsa_circ_236867,RMVar_hsa_circ_236865,RMVar_hsa_circ_328816,RMVar_hsa_circ_55813,RMVar_hsa_circ_236869,RMVar_hsa_circ_97473,RMVar_hsa_circ_122135,RMVar_hsa_circ_376358,RMVar_hsa_circ_236870,RMVar_hsa_circ_236868 58565 RMVar_ID_58565 Human_SNP_ID_264215266 m1A Human chr6 - 604790 604790 604790 GTGGAGGGAGGCAGGTGTGTCCCCGCGGGGCCAGCGCGTGAGTTCAGAGACAAGCAGAGGCCAGC GTGGAGGGAGGCAGGTGTGTCCCCGCGGGGCCCGCGCGTGAGTTCAGAGACAAGCAGAGGCCAGC T G EXOC2 Ensembl:ENSG00000112685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:604638..604890 26863196 MeRIP-seq:(Medium) rs1254033761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102003,RMVar_hsa_circ_236834,RMVar_hsa_circ_77053,RMVar_hsa_circ_236840,RMVar_hsa_circ_6820,RMVar_hsa_circ_236836,RMVar_hsa_circ_236837,RMVar_hsa_circ_119454,RMVar_hsa_circ_323684,RMVar_hsa_circ_349621,RMVar_hsa_circ_299755,RMVar_hsa_circ_53068,RMVar_hsa_circ_284225,RMVar_hsa_circ_120841,RMVar_hsa_circ_236838,RMVar_hsa_circ_236839,RMVar_hsa_circ_236849,RMVar_hsa_circ_375807,RMVar_hsa_circ_46551,RMVar_hsa_circ_372533,RMVar_hsa_circ_52101,RMVar_hsa_circ_20539,RMVar_hsa_circ_81930,RMVar_hsa_circ_236852,RMVar_hsa_circ_236853,RMVar_hsa_circ_98963,RMVar_hsa_circ_339929,RMVar_hsa_circ_90299,RMVar_hsa_circ_236855,RMVar_hsa_circ_236856,RMVar_hsa_circ_22652,RMVar_hsa_circ_291055,RMVar_hsa_circ_236857,RMVar_hsa_circ_324410,RMVar_hsa_circ_236860,RMVar_hsa_circ_16708,RMVar_hsa_circ_330273,RMVar_hsa_circ_103696,RMVar_hsa_circ_236863,RMVar_hsa_circ_14054,RMVar_hsa_circ_236862,RMVar_hsa_circ_236866,RMVar_hsa_circ_302601,RMVar_hsa_circ_352153,RMVar_hsa_circ_373708,RMVar_hsa_circ_329232,RMVar_hsa_circ_287227,RMVar_hsa_circ_236867,RMVar_hsa_circ_236865,RMVar_hsa_circ_328816,RMVar_hsa_circ_55813,RMVar_hsa_circ_236869,RMVar_hsa_circ_97473,RMVar_hsa_circ_122135,RMVar_hsa_circ_376358,RMVar_hsa_circ_236870,RMVar_hsa_circ_236868 58566 RMVar_ID_58566 Human_SNP_ID_264368361 m1A Human chr6 - 1205183 1205171 1205184 TGGGTGCTGGGATAGAGTGGGTGCTGGGATGAAGTGGGTGCTGGGATACAGTGGGTGCTGGGATA TGGGTGCTGGGATAGAGTGGGTGCTGGGATG_____________GATACAGTGGGTGCTGGGATA CCCAGCACCCACTT C lnc-GMDS-21-001,lnc-GMDS-24 RNACentral:URS00008B445B,RNACentral:URS00008B9B5E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1205156..1205294 26863196 MeRIP-seq:(Medium) rs1468840879 Functional Loss DEL dbSNP153 32..44 33 - - - 58567 RMVar_ID_58567 Human_SNP_ID_264368414 m1A Human chr6 - 1205251 1205243 1205252 TGGGTGCTGGGATAGAGCGGGTGCTGGGATAGAGTGGGTGCTGGGATGAAGTGGGTGCTGGGATA TGGGTGCTGGGATAGAGCGGGTGCTGGGATA_________CTGGGATGAAGTGGGTGCTGGGATA GCACCCACTC G lnc-GMDS-21-001,lnc-GMDS-24 RNACentral:URS00008B445B,RNACentral:URS00008B9B5E lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:1205143..1205298 26863196 MeRIP-seq:(Medium) rs1561729900 Functional Loss DEL dbSNP153 32..40 33 - - - 58568 RMVar_ID_58568 Human_SNP_ID_264368523 m1A Human chr6 - 1205508 1205508 1205508 AGCGGGTGCTGGGATGAAGTGGGTGCTGGGATACAGTGGGTGCTGGGATAGAGCGGGTGCTGGGA AGCGGGTGCTGGGATGAAGTGGGTGCTGGGATGCAGTGGGTGCTGGGATAGAGCGGGTGCTGGGA T C lnc-GMDS-21-001,lnc-GMDS-24 RNACentral:URS00008B445B,RNACentral:URS00008B9B5E lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1205455..1205525 26863196 MeRIP-seq:(Medium) rs1409018563 Functional Loss SNV dbSNP153 33..33 33 - - - 58569 RMVar_ID_58569 Human_SNP_ID_264368716 m1A Human chr6 + 1205815 1205812 1205815 CCCAGCACCTGCTCTATCCCAGCACCCACTCTATCCCAGCACCCACTCTATCCCAGCACCCACTC CCCAGCACCTGCTCTATCCCAGCACCCACT___TCCCAGCACCCACTCTATCCCAGCACCCACTC TCTA T lnc-FOXQ1-11,NONHSAG042575.2,lnc-FOXQ1-11:2,RF00017-1190 RNACentral:URS00009BB774,RNACentral:URS00009AF878,RNACentral:URS00009AFC6C,RNACentral:URS000092EF5C lincRNA,lincRNA,lincRNA,SRP RNA intron,exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1205766..1205851 26863196 MeRIP-seq:(Medium) rs1316516637 Functional Loss DEL dbSNP153 31..33 33 - - - 58570 RMVar_ID_58570 Human_SNP_ID_264395190 m1A Human chr6 + 1312463 1312463 1312463 CCCCAAAGTCTCAACGTCGAACCGAAGGCGACACCCACCCAACTCCTCCCTCTCCGCCCCATAGT CCCCAAAGTCTCAACGTCGAACCGAAGGCGACGCCCACCCAACTCCTCCCTCTCCGCCCCATAGT A G FOXQ1 Ensembl:ENSG00000164379 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1312414..1312610 26863196 MeRIP-seq:(Medium) rs1303974644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791069,Human_RBP_ID_27519363 58571 RMVar_ID_58571 Human_SNP_ID_264395319 m1A Human chr6 + 1312784 1312784 1312784 GGGCAGTGACCTGGAGGGCGCGGGCGGCAGCGACGCGCCGTCCCCGCTGTCGGCGGCGGGAGACG GGGCAGTGACCTGGAGGGCGCGGGCGGCAGCGCCGCGCCGTCCCCGCTGTCGGCGGCGGGAGACG A C FOXQ1 Ensembl:ENSG00000164379 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1312734..1313142 26863196 MeRIP-seq:(Medium) rs1446955656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791710,Human_RBP_ID_4903055,Human_RBP_ID_5152271,Human_RBP_ID_9354672,Human_RBP_ID_9399815,Human_RBP_ID_18465678,Human_RBP_ID_22106624,Human_RBP_ID_22728059,Human_RBP_ID_23116485 58572 RMVar_ID_58572 Human_SNP_ID_264395384 m1A Human chr6 + 1312878 1312878 1312878 GCCAACAGCCCGGCCGCGGGCGGCGGCGCCAGAGATACGCAGGGCGACGGCGAACAGAGTGCGGG GCCAACAGCCCGGCCGCGGGCGGCGGCGCCAGGGATACGCAGGGCGACGGCGAACAGAGTGCGGG A G FOXQ1 Ensembl:ENSG00000164379 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:1312756..1313127 26863196 MeRIP-seq:(Medium) rs1278727194 Functional Loss SNV dbSNP153 33..33 33 - - - 58573 RMVar_ID_58573 Human_SNP_ID_264395385 m1A Human chr6 + 1312878 1312878 1312878 GCCAACAGCCCGGCCGCGGGCGGCGGCGCCAGAGATACGCAGGGCGACGGCGAACAGAGTGCGGG GCCAACAGCCCGGCCGCGGGCGGCGGCGCCAGTGATACGCAGGGCGACGGCGAACAGAGTGCGGG A T FOXQ1 Ensembl:ENSG00000164379 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:1312756..1313127 26863196 MeRIP-seq:(Medium) rs1278727194 Functional Loss SNV dbSNP153 33..33 33 - - - 58574 RMVar_ID_58574 Human_SNP_ID_264395734 m1A Human chr6 + 1313501 1313501 1313501 CCGCCAGGAGGAGCGCGCCAGCCCCGCGGGCAAGTTCTCCAGCTCCTTCGCCATCGACAGCATCC CCGCCAGGAGGAGCGCGCCAGCCCCGCGGGCAGGTTCTCCAGCTCCTTCGCCATCGACAGCATCC A G FOXQ1 Ensembl:ENSG00000164379 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1313452..1313815 26863196 MeRIP-seq:(Medium) rs773920812 Functional Loss SNV dbSNP153 33..33 33 - - - 58575 RMVar_ID_58575 Human_SNP_ID_264415176 m1A Human chr6 + 1390075 1390075 1390075 CGCCGCCGCCGCCGCCGCCGCCGCCGCCCCGGAGACCACCTCCTCCTCCTCGTCGTCGTCCTCCG CGCCGCCGCCGCCGCCGCCGCCGCCGCCCCGGGGACCACCTCCTCCTCCTCGTCGTCGTCCTCCG A G FOXF2 Ensembl:ENSG00000137273 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:1389975..1390145 26863196 MeRIP-seq:(Medium) rs900625813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27519702 58576 RMVar_ID_58576 Human_SNP_ID_264415178 m1A Human chr6 - 1390083 1390080 1390083 GCAGGAGGCGGAGGACGACGACGAGGAGGAGGAGGTGGTCTCCGGGGCGGCGGCGGCGGCGGCGG GCAGGAGGCGGAGGACGACGACGAGGAGGAGG___TGGTCTCCGGGGCGGCGGCGGCGGCGGCGG ACCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1389576..1390320 26863196 MeRIP-seq:(Medium) rs769821909 Functional Loss DEL dbSNP153 33..35 33 - - - 58577 RMVar_ID_58577 Human_SNP_ID_264415204 m1A Human chr6 - 1390122 1390122 1390122 GGGGGCGCTGGCCGAATTGGAGGAGGACGAGGACGAGGCGCAGGAGGCGGAGGACGACGACGAGG GGGGGCGCTGGCCGAATTGGAGGAGGACGAGGGCGAGGCGCAGGAGGCGGAGGACGACGACGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:1389559..1390440;chr6:1389526..1390450 26863196 MeRIP-seq:(Medium) rs1490467102 Functional Loss SNV dbSNP153 33..33 33 - - - 58578 RMVar_ID_58578 Human_SNP_ID_264474262 m1A Human chr6 - 1609555 1609555 1609555 GACTTCCTGGGTCCTCCCGGGACCCCGTGCAGACCCTTCCTTCGCCCACGGCTCCCGAGTGGCCC GACTTCCTGGGTCCTCCCGGGACCCCGTGCAGCCCCTTCCTTCGCCCACGGCTCCCGAGTGGCCC T G lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1609505..1609653 26863196 MeRIP-seq:(Medium) rs1486299378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4908733,Human_RBP_ID_5477562 58579 RMVar_ID_58579 Human_SNP_ID_264474317 m1A Human chr6 + 1609725 1609725 1609725 GCCGGCGCGGGCGCAGGGCCGGGGCCCGGGCCAGGGCGGCCGGCGCGCGTGTGGTCAGCCCCGCG GCCGGCGCGGGCGCAGGGCCGGGGCCCGGGCCGGGGCGGCCGGCGCGCGTGTGGTCAGCCCCGCG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr6:1609626..1609750;chr6:1609642..1609724 26863410 MeRIP-seq:(Medium) rs912813991 Functional Loss SNV dbSNP153 33..33 33 - - - 58580 RMVar_ID_58580 Human_SNP_ID_264474440 m1A Human chr6 + 1609977 1609977 1609977 TCCTTAAGCGGCTGGCGCGCGAGAGACCGAGAAAAGGTGACGCGGGGCCCGGGCAGGCGGCCGGC TCCTTAAGCGGCTGGCGCGCGAGAGACCGAGACAAGGTGACGCGGGGCCCGGGCAGGCGGCCGGC A C FOXC1 Ensembl:ENSG00000054598 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1609926..1610506 26863196 MeRIP-seq:(Medium) rs1554100871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1325696,Human_RBP_ID_4872175 58581 RMVar_ID_58581 Human_SNP_ID_264474518 m1A Human chr6 - 1610034 1610034 1610034 CCTGAGCTGCCGGCGAAGGCGGCCAAATAACCAGGGCGGGGGGGGGGGGGGCCGCGCGCCGGCCG CCTGAGCTGCCGGCGAAGGCGGCCAAATAACCGGGGCGGGGGGGGGGGGGGCCGCGCGCCGGCCG T C lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:1609933..1610197 26863410 MeRIP-seq:(Medium) rs1224309145 Functional Loss SNV dbSNP153 33..33 33 - - - 58582 RMVar_ID_58582 Human_SNP_ID_264474519 m1A Human chr6 - 1610034 1610034 1610034 CCTGAGCTGCCGGCGAAGGCGGCCAAATAACCAGGGCGGGGGGGGGGGGGGCCGCGCGCCGGCCG CCTGAGCTGCCGGCGAAGGCGGCCAAATAACCCGGGCGGGGGGGGGGGGGGCCGCGCGCCGGCCG T G lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:1609933..1610197 26863410 MeRIP-seq:(Medium) rs1224309145 Functional Loss SNV dbSNP153 33..33 33 - - - 58583 RMVar_ID_58583 Human_SNP_ID_264474587 m1A Human chr6 - 1610207 1610201 1610208 CGGCCGCGAGGCGGGGTCGCTGCGAGGGGAGAAGGCCGGGCCCGGCCGCGGCAGACCGCCTTGCA CGGCCGCGAGGCGGGGTCGCTGCGAGGGGAG_______GGCCCGGCCGCGGCAGACCGCCTTGCA CCGGCCTT C lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:1609926..1610750 26863410 MeRIP-seq:(Medium) rs1248072663 Functional Loss DEL dbSNP153 32..38 33 - - - 58584 RMVar_ID_58584 Human_SNP_ID_264474674 m1A Human chr6 - 1610404 1610404 1610404 TCGCCGCCGCCCCGCGCCGCCCGCCGCCCCCCACCCTCGCTCGGGCCGGGCCGCGCCGCGCCGGC TCGCCGCCGCCCCGCGCCGCCCGCCGCCCCCCCCCCTCGCTCGGGCCGGGCCGCGCCGCGCCGGC T G lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,H2O2 treatment;HEK293T,Starvation treatment chr6:1610319..1610469;chr6:1610324..1610440 26863410 MeRIP-seq:(Medium) rs1002267010 Functional Loss SNV dbSNP153 33..33 33 - - - 58585 RMVar_ID_58585 Human_SNP_ID_264474975 m1A Human chr6 + 1611007 1611007 1611007 AGGACGCGGTGAAGGACAAGGAGGAGAAGGACAGGCTGCACCTCAAGGAGCCGCCCCCGCCCGGC AGGACGCGGTGAAGGACAAGGAGGAGAAGGACGGGCTGCACCTCAAGGAGCCGCCCCCGCCCGGC A G FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:1610875..1611400;chr6:1610876..1612299 26863196 MeRIP-seq:(Medium) rs1485684451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3800038,Human_RBP_ID_7568524 58586 RMVar_ID_58586 Human_SNP_ID_264475035 m1A Human chr6 - 1611107 1611107 1611107 TACCGTTCTCGGTCTTGATGTCCTGGATGCGCACGGGCGGCGGCTGCGGACCGGGCGCGTTGCCG TACCGTTCTCGGTCTTGATGTCCTGGATGCGCGCGGGCGGCGGCTGCGGACCGGGCGCGTTGCCG T C lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:1610951..1612025 26863410 MeRIP-seq:(Medium) rs768405602 Functional Loss SNV dbSNP153 33..33 33 - - - 58587 RMVar_ID_58587 Human_SNP_ID_264475053 m1A Human chr6 - 1611138 1611138 1611138 GGGGACAGGGGCTGGGGCGGCGAGGGGCACGTACCGTTCTCGGTCTTGATGTCCTGGATGCGCAC GGGGACAGGGGCTGGGGCGGCGAGGGGCACGTGCCGTTCTCGGTCTTGATGTCCTGGATGCGCAC T C lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1610834..1611363 26863196 MeRIP-seq:(Medium) rs1160038006 Functional Loss SNV dbSNP153 33..33 33 - - - 58588 RMVar_ID_58588 Human_SNP_ID_264475080 m1A Human chr6 + 1611193 1611173 1611194 CCCTGTCCCCGGCCGCCGCCCTGGGCAGCGGCAGCGCCGCCGCGGTGCCCAAGATCGAGAGCCCC CCCTGTCCCCGGC_____________________CGCCGCCGCGGTGCCCAAGATCGAGAGCCCC CCGCCGCCCTGGGCAGCGGCAG C FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:1611093..1611238 26863196 MeRIP-seq:(Medium) rs1019610153 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_251949,Human_RBP_ID_4872238 58589 RMVar_ID_58589 Human_SNP_ID_264475322 m1A Human chr6 + 1611562 1611562 1611562 GCTCCCCCTGCAGCCAGACCTCCAGCGCGGGCAGCTCGGGCGGCGGCGGCGGCGGCGCGGGGGCC GCTCCCCCTGCAGCCAGACCTCCAGCGCGGGCCGCTCGGGCGGCGGCGGCGGCGGCGCGGGGGCC A C FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1611536..1611975 26863196 MeRIP-seq:(Medium) rs1270754997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251950,Human_RBP_ID_7568537 58590 RMVar_ID_58590 Human_SNP_ID_264475509 m1A Human chr6 + 1611842 1611839 1611842 AGGCCAGGAGGCCGGCCACCACCCTGCGGCCCACCAAGGCCGCCTCACCTCGTGGTACCTGAACC AGGCCAGGAGGCCGGCCACCACCCTGCGGC___CCAAGGCCGCCTCACCTCGTGGTACCTGAACC CCCA C FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:1611511..1612009 26863196 MeRIP-seq:(Medium) rs971780796 Functional Loss DEL dbSNP153 31..33 33 - - - 58591 RMVar_ID_58591 Human_SNP_ID_264475558 m1A Human chr6 + 1611930 1611930 1611930 TTGGCGAGCGCGGCGGCGGCGGCGGCGGCCGCAGGCTACCCGGGCCAGCAGCAGAACTTCCACTC TTGGCGAGCGCGGCGGCGGCGGCGGCGGCCGCGGGCTACCCGGGCCAGCAGCAGAACTTCCACTC A G FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1611458..1612212 26863196 MeRIP-seq:(Medium) rs1334903055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251952,Human_RBP_ID_22829937 58592 RMVar_ID_58592 Human_SNP_ID_264475630 m1A Human chr6 - 1612057 1612057 1612057 GTAGACGAAAGCTCCGGACGTGCGGTACAGAGACTGGCTGGAAGGGAAGGCCATTTGACAGCTAC GTAGACGAAAGCTCCGGACGTGCGGTACAGAGTCTGGCTGGAAGGGAAGGCCATTTGACAGCTAC T A lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:1612007..1612107 26863196 MeRIP-seq:(Medium) rs1278204046 Functional Loss SNV dbSNP153 33..33 33 - - - 58593 RMVar_ID_58593 Human_SNP_ID_264508550 m1A Human chr6 + 1738002 1737996 1738002 ACACATACACACACACCACAAACACACCACACACACAGACACACATACACACATACACACACCAC ACACATACACACACACCACAAACACAC______CACAGACACACATACACACATACACACACCAC CCACACA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1737999..1738110 26863196 MeRIP-seq:(Medium) rs1212464966 Functional Loss DEL dbSNP153 28..33 33 - - - 58594 RMVar_ID_58594 Human_SNP_ID_264508551 m1A Human chr6 + 1738002 1737996 1738002 ACACATACACACACACCACAAACACACCACACACACAGACACACATACACACATACACACACCAC ACACATACACACACACCACAAACACACCA____CACAGACACACATACACACATACACACACCAC CCACACA CCA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1737999..1738110 26863196 MeRIP-seq:(Medium) rs1212464966 Functional Loss DEL dbSNP153 30..33 33 - - - 58595 RMVar_ID_58595 Human_SNP_ID_264508552 m1A Human chr6 + 1738002 1737996 1738002 ACACATACACACACACCACAAACACACCACACACACAGACACACATACACACATACACACACCAC ACACATACACACACACCACAAACACACCACA__CACAGACACACATACACACATACACACACCAC CCACACA CCACA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1737999..1738110 26863196 MeRIP-seq:(Medium) rs1212464966 Functional Loss DEL dbSNP153 32..33 33 - - - 58596 RMVar_ID_58596 Human_SNP_ID_264547594 m1A Human chr6 + 1898094 1898094 1898094 GACACCTACCCTGGCCTCCCTTGCCATCCTGGACACCTATCCTGGCCTCCCTTGCCATCCTGGAC GACACCTACCCTGGCCTCCCTTGCCATCCTGGGCACCTATCCTGGCCTCCCTTGCCATCCTGGAC A G lnc-FOXC1-9,lnc-FOXC1-9:2,lnc-FOXC1-9:3,lnc-FOXC1-9:4,lnc-FOXC1-9:5,lnc-FOXC1-9:6 RNACentral:URS00008BBBEB,RNACentral:URS00008BF06D,RNACentral:URS00008B94CF,RNACentral:URS00008B33FE,RNACentral:URS00008BA595,RNACentral:URS00008BAF01 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1898061..1898212 26863196 MeRIP-seq:(Medium) rs1391791055 Functional Loss SNV dbSNP153 33..33 33 - - - 58597 RMVar_ID_58597 Human_SNP_ID_264547595 m1A Human chr6 - 1898101 1898101 1898101 GGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGATAGGTGTCCAGGATGGCAAGGGAGGCCAGGGT GGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGGT T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:1897899..1898234;chr6:1897952..1898133 26863196 MeRIP-seq:(Medium) rs9501781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18956956 RMVar_hsa_circ_74524 58598 RMVar_ID_58598 Human_SNP_ID_264570768 m1A Human chr6 - 1991117 1991117 1991117 TACACTCCAGTGACTTGTCTGTTTTCTGGGTGAGGTAAGGGGATAGTCTGCTGGAGAATAAGAGG TACACTCCAGTGACTTGTCTGTTTTCTGGGTGTGGTAAGGGGATAGTCTGCTGGAGAATAAGAGG T A GMDS Ensembl:ENSG00000112699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:1991115..1991367 26863196 MeRIP-seq:(Medium) rs538693285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65797,RMVar_hsa_circ_280126,RMVar_hsa_circ_236883,RMVar_hsa_circ_236881,RMVar_hsa_circ_376247 58599 RMVar_ID_58599 Human_SNP_ID_264601319 m1A Human chr6 - 2112707 2112707 2112707 GATTTGTGACGTTTTAAAGAAACATTTTAGTGATGTGACAGAAGAACTTGGCCAGCGTGCAAGGG GATTTGTGACGTTTTAAAGAAACATTTTAGTGGTGTGACAGAAGAACTTGGCCAGCGTGCAAGGG T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:2112706..2112820 26863196 MeRIP-seq:(Medium) rs1272773764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15764118 RMVar_hsa_circ_65797,RMVar_hsa_circ_280126,RMVar_hsa_circ_236883,RMVar_hsa_circ_236881,RMVar_hsa_circ_376247 58600 RMVar_ID_58600 Human_SNP_ID_264601446 m1A Human chr6 + 2113201 2113201 2113201 ACTGGTTCTATTGACCTTCTGGTCCCCTGGGCACTGGAGCCCTGGGTTTCCCTCTTCTCTAGTGA ACTGGTTCTATTGACCTTCTGGTCCCCTGGGCCCTGGAGCCCTGGGTTTCCCTCTTCTCTAGTGA A C lnc-FOXC1-12,lnc-FOXC1-12:2,lnc-FOXC1-12:3 RNACentral:URS00008C0678,RNACentral:URS00008B507E,RNACentral:URS00008BB85E lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:2113196..2113419 26863196 MeRIP-seq:(Medium) rs913351350 Functional Loss SNV dbSNP153 33..33 33 - - - 58601 RMVar_ID_58601 Human_SNP_ID_264608216 m1A Human chr6 - 2141857 2141857 2141857 AGAGAGAGAGAGAGAGAGAGAGAGCACGCACAACCAAAACCAAACCCAGACTTCCCAGTGTGTCG AGAGAGAGAGAGAGAGAGAGAGAGCACGCACAGCCAAAACCAAACCCAGACTTCCCAGTGTGTCG T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:2141855..2141939 26863196 MeRIP-seq:(Medium) rs1204210680 Functional Loss SNV dbSNP153 33..33 33 - - - 58602 RMVar_ID_58602 Human_SNP_ID_264633795 m1A Human chr6 + 2245473 2245457 2245473 GGTCGGCGGCAGGGCGGAGCGCGGCAGAGGGCAGGCGCGGTGCCGGCAGGAACGCGGGGGTGTGC GGTCGGCGGCAGGGCGG________________GGCGCGGTGCCGGCAGGAACGCGGGGGTGTGC GAGCGCGGCAGAGGGCA G lnc-WRNIP1-3 RNACentral:URS00008B99F2 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr6:2245351..2245572;chr6:2245426..2245577 26863196 MeRIP-seq:(Medium) rs781549210 Functional Loss DEL dbSNP153 18..33 33 - - - 58603 RMVar_ID_58603 Human_SNP_ID_264633803 m1A Human chr6 + 2245473 2245473 2245473 GGTCGGCGGCAGGGCGGAGCGCGGCAGAGGGCAGGCGCGGTGCCGGCAGGAACGCGGGGGTGTGC GGTCGGCGGCAGGGCGGAGCGCGGCAGAGGGCGGGCGCGGTGCCGGCAGGAACGCGGGGGTGTGC A G lnc-WRNIP1-3 RNACentral:URS00008B99F2 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr6:2245351..2245572;chr6:2245426..2245577 26863196 MeRIP-seq:(Medium) rs1225716559 Functional Loss SNV dbSNP153 33..33 33 - - - 58604 RMVar_ID_58604 Human_SNP_ID_264633835 m1A Human chr6 + 2245550 2245550 2245550 CTCTCCAGGCTGCGGGCAGGGAGGGAGAGCGCACCGCGCGACCGGCCGCCACAGTCTGACAGGGG CTCTCCAGGCTGCGGGCAGGGAGGGAGAGCGCCCCGCGCGACCGGCCGCCACAGTCTGACAGGGG A C lnc-WRNIP1-3 RNACentral:URS00008B99F2 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:2245401..2245600 26863196 MeRIP-seq:(Medium) rs910250977 Functional Loss SNV dbSNP153 33..33 33 - - - 58605 RMVar_ID_58605 Human_SNP_ID_264639437 m1A Human chr6 + 2268200 2268195 2268201 AGGAAATAGTGGCTGGAGAGTGGTTACTTGAAACTGAGTTTATGGCAAGGATGTAGAGGGGTGTG AGGAAATAGTGGCTGGAGAGTGGTTACT______TGAGTTTATGGCAAGGATGTAGAGGGGTGTG TTGAAAC T GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:2268033..2268230 26863196 MeRIP-seq:(Medium) rs1359163777 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_15765858 RMVar_hsa_circ_75731,RMVar_hsa_circ_236887,RMVar_hsa_circ_98527,RMVar_hsa_circ_354242,RMVar_hsa_circ_271586,RMVar_hsa_circ_236889,RMVar_hsa_circ_236890,RMVar_hsa_circ_236891,RMVar_hsa_circ_236888 58606 RMVar_ID_58606 Human_SNP_ID_264666465 m1A Human chr6 + 2376421 2376421 2376421 CACACACAAACCTCCAAATATACCCAACACACACACCAACCCAATGCATTACACACACATATACA CACACACAAACCTCCAAATATACCCAACACACGCACCAACCCAATGCATTACACACACATATACA A G GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:2376377..2376494 26863196 MeRIP-seq:(Medium) rs945628699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214552,Human_RBP_ID_267267,Human_RBP_ID_9437312,Human_RBP_ID_26764306 RMVar_hsa_circ_354242,RMVar_hsa_circ_32701,RMVar_hsa_circ_236893,RMVar_hsa_circ_236892,RMVar_hsa_circ_236894 58607 RMVar_ID_58607 Human_SNP_ID_264687637 m1A Human chr6 - 2468159 2468159 2468159 TGGATCTCACCACCCCTGCAGCCCAGACTCCGACTCTCTCTCTCTCCCCTTCCTCTCCCTGTCTA TGGATCTCACCACCCCTGCAGCCCAGACTCCGTCTCTCTCTCTCTCCCCTTCCTCTCCCTGTCTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:2468119..2468215 26863196 MeRIP-seq:(Medium) rs1460197196 Functional Loss SNV dbSNP153 33..33 33 - - - 58608 RMVar_ID_58608 Human_SNP_ID_264761978 m1A Human chr6 - 2765571 2765571 2765571 GGCGCCCGGCGCGGCCGCAGCAACCCGTGCGCACGCGGAGGCCTTCGATGCCCTCCGCTAGGCCC GGCGCCCGGCGCGGCCGCAGCAACCCGTGCGCCCGCGGAGGCCTTCGATGCCCTCCGCTAGGCCC T G lnc-MYLK4-1 RNACentral:URS00008C135C lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:2765529..2765655 26863196 MeRIP-seq:(Medium) rs949790717 Functional Loss SNV dbSNP153 33..33 33 - - - 58609 RMVar_ID_58609 Human_SNP_ID_264762019 m1A Human chr6 + 2765608 2765608 2765608 ACGGGTTGCTGCGGCCGCGCCGGGCGCCGGGGAGGGCGGCGGCCGCCATGGAGGTGAGCGGGCCG ACGGGTTGCTGCGGCCGCGCCGGGCGCCGGGGGGGGCGGCGGCCGCCATGGAGGTGAGCGGGCCG A G WRNIP1 Ensembl:ENSG00000124535 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:2765512..2766010 26863410 MeRIP-seq:(Medium) rs979830713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903060,Human_RBP_ID_8905613 58610 RMVar_ID_58610 Human_SNP_ID_264762093 m1A Human chr6 + 2765701 2765701 2765701 ACCAGGTGCAGTGCCCCGTGTGCCAGCAGATGATGCCCGCCGCGCACATCAACTCGCACCTGGAC ACCAGGTGCAGTGCCCCGTGTGCCAGCAGATGCTGCCCGCCGCGCACATCAACTCGCACCTGGAC A C WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2765661..2765762 32194978 MeRIP-seq:(Medium) rs913649122 Functional Loss SNV dbSNP153 33..33 33 - - - 58611 RMVar_ID_58611 Human_SNP_ID_264762112 m1A Human chr6 - 2765722 2765722 2765722 CGGGTGGAGCAGCAGACAGCGGTCCAGGTGCGAGTTGATGTGCGCGGCGGGCATCATCTGCTGGC CGGGTGGAGCAGCAGACAGCGGTCCAGGTGCGCGTTGATGTGCGCGGCGGGCATCATCTGCTGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:2765554..2765854 26863196 MeRIP-seq:(Medium) rs763635770 Functional Loss SNV dbSNP153 33..33 33 - - - 58612 RMVar_ID_58612 Human_SNP_ID_264762374 m1A Human chr6 + 2766073 2766073 2766073 GGAAGAGGCCGGCGGCCGCCGCCGCGGCGGGGAGCGCGTCTCCGCGCAGCTGGGACGAGGCGGAG GGAAGAGGCCGGCGGCCGCCGCCGCGGCGGGGGGCGCGTCTCCGCGCAGCTGGGACGAGGCGGAG A G WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:2765901..2766200 26863196 MeRIP-seq:(Medium) rs1044893495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8905042 58613 RMVar_ID_58613 Human_SNP_ID_264762409 m1A Human chr6 + 2766122 2766122 2766122 CTGGGACGAGGCGGAGGCGCAGGAGGAGGAGGAGGCCGTGGGCGACGGCGATGGCGACGGGGACG CTGGGACGAGGCGGAGGCGCAGGAGGAGGAGGCGGCCGTGGGCGACGGCGATGGCGACGGGGACG A C WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T cell line,total RNA;HEK293T,H2O2 treatment chr6:2766048..2766277;chr6:2766059..2766159 26863196,26863410 MeRIP-seq:(Medium) rs981681990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9309068,Human_RBP_ID_18472190 RMVar_hsa_circ_236897 58614 RMVar_ID_58614 Human_SNP_ID_264762420 m1A Human chr6 - 2766141 2766129 2766141 TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCCATCGCCGTCGCCCACGGCCTCCTCCTCCTCCTG TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCC____________CACGGCCTCCTCCTCCTCCTG GGGCGACGGCGAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:2765389..2766441;chr6:2765351..2768750;chr6:2765376..2766450;chr6:2765351..2766450 26863196 MeRIP-seq:(Medium) rs535821800 Functional Loss DEL dbSNP153 33..44 33 - - - 58615 RMVar_ID_58615 Human_SNP_ID_264762429 m1A Human chr6 - 2766141 2766135 2766141 TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCCATCGCCGTCGCCCACGGCCTCCTCCTCCTCCTG TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCC______GTCGCCCACGGCCTCCTCCTCCTCCTG CGGCGAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:2765389..2766441;chr6:2765351..2768750;chr6:2765376..2766450;chr6:2765351..2766450 26863196 MeRIP-seq:(Medium) rs984238283 Functional Loss DEL dbSNP153 33..38 33 - - - 58616 RMVar_ID_58616 Human_SNP_ID_264762433 m1A Human chr6 + 2766152 2766141 2766153 GGAGGCCGTGGGCGACGGCGATGGCGACGGGGACGCGGACGCGGACGGCGAGGACGACCCGGGGC GGAGGCCGTGGGCGACGGCGAT____________GCGGACGCGGACGGCGAGGACGACCCGGGGC TGGCGACGGGGAC T WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:2766026..2766200 26863196 MeRIP-seq:(Medium) rs1395438803 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_9309068,Human_RBP_ID_18472190 RMVar_hsa_circ_236897 58617 RMVar_ID_58617 Human_SNP_ID_264762437 m1A Human chr6 + 2766146 2766146 2766146 GGAGGAGGAGGCCGTGGGCGACGGCGATGGCGACGGGGACGCGGACGCGGACGGCGAGGACGACC GGAGGAGGAGGCCGTGGGCGACGGCGATGGCGGCGGGGACGCGGACGCGGACGGCGAGGACGACC A G WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:2765676..2766491 26863196 MeRIP-seq:(Medium) rs1483731459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9309068,Human_RBP_ID_18472190 RMVar_hsa_circ_236897 58618 RMVar_ID_58618 Human_SNP_ID_264762492 m1A Human chr6 - 2766221 2766221 2766221 GGGGGTGCGGGCGGCCCCCGCCACTGGCCCCGAAGGCGGTGGCGGCTTCGGCAGCGTCCGCGTCC GGGGGTGCGGGCGGCCCCCGCCACTGGCCCCGCAGGCGGTGGCGGCTTCGGCAGCGTCCGCGTCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:2765860..2766290 26863410 MeRIP-seq:(Medium) rs1193157455 Functional Loss SNV dbSNP153 33..33 33 - - - 58619 RMVar_ID_58619 Human_SNP_ID_264762595 m1A Human chr6 - 2766314 2766314 2766314 GCCCGAAGTAATCCTGCAGCGTGTCAGGACGCATCGTGTCGGCCAGCGGCTTGCCCTGTAGCATC GCCCGAAGTAATCCTGCAGCGTGTCAGGACGCGTCGTGTCGGCCAGCGGCTTGCCCTGTAGCATC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:2766264..2766481 26863196 MeRIP-seq:(Medium) rs1305870473 Functional Loss SNV dbSNP153 33..33 33 - - - 58620 RMVar_ID_58620 Human_SNP_ID_264762669 m1A Human chr6 - 2766404 2766404 2766404 AGCCCGGCGGCCCCCACAGGATAAGCGAGGGGATTTCGTTGGTCTCCAGGAGCGAGCGCAGCAGG AGCCCGGCGGCCCCCACAGGATAAGCGAGGGGCTTTCGTTGGTCTCCAGGAGCGAGCGCAGCAGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2766357..2770338 32194978 MeRIP-seq:(Medium) rs759102231 Functional Loss SNV dbSNP153 33..33 33 - - - 58621 RMVar_ID_58621 Human_SNP_ID_264766659 m1A Human chr6 + 2779420 2779420 2779420 TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCAGTAGAGTTCTGATCACAGAGAATGACGTGAAG TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCGGTAGAGTTCTGATCACAGAGAATGACGTGAAG A G WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:2779251..2785350 32194978 MeRIP-seq:(Medium) rs1182152203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659868,Human_RBP_ID_2017201,Human_RBP_ID_8899400,Human_RBP_ID_9308109,Human_RBP_ID_15773178,Human_RBP_ID_18072053,Human_RBP_ID_22513842,Human_RBP_ID_23059251 Human_Splice_Rec_733311,Human_Splice_Rec_733323,Human_Splice_Rec_733335,Human_Splice_Rec_733347,Human_Splice_Rec_733357 Human_miRNA_ID_2211918,Human_miRNA_ID_2568006 RMVar_hsa_circ_13644,RMVar_hsa_circ_283108,RMVar_hsa_circ_309443,RMVar_hsa_circ_365013,RMVar_hsa_circ_236901,RMVar_hsa_circ_125205,RMVar_hsa_circ_289201,RMVar_hsa_circ_370942,RMVar_hsa_circ_277934,RMVar_hsa_circ_236902,RMVar_hsa_circ_236899,RMVar_hsa_circ_236900 58622 RMVar_ID_58622 Human_SNP_ID_264766660 m1A Human chr6 + 2779420 2779420 2779420 TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCAGTAGAGTTCTGATCACAGAGAATGACGTGAAG TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCTGTAGAGTTCTGATCACAGAGAATGACGTGAAG A T WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:2779251..2785350 32194978 MeRIP-seq:(Medium) rs1182152203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659868,Human_RBP_ID_2017201,Human_RBP_ID_8899400,Human_RBP_ID_9308109,Human_RBP_ID_15773178,Human_RBP_ID_18072053,Human_RBP_ID_22513842,Human_RBP_ID_23059251 Human_Splice_Rec_733311,Human_Splice_Rec_733323,Human_Splice_Rec_733335,Human_Splice_Rec_733347,Human_Splice_Rec_733357 Human_miRNA_ID_2211918,Human_miRNA_ID_2568006 RMVar_hsa_circ_13644,RMVar_hsa_circ_283108,RMVar_hsa_circ_309443,RMVar_hsa_circ_365013,RMVar_hsa_circ_236901,RMVar_hsa_circ_125205,RMVar_hsa_circ_289201,RMVar_hsa_circ_370942,RMVar_hsa_circ_277934,RMVar_hsa_circ_236902,RMVar_hsa_circ_236899,RMVar_hsa_circ_236900 58623 RMVar_ID_58623 Human_SNP_ID_264768034 m1A Human chr6 + 2783499 2783499 2783499 CGCCTCCCTCTACTGGCTGGCTCGCATGCTCGAGGGAGGAGAGGACCCACTCTACGTGGCACGGA CGCCTCCCTCTACTGGCTGGCTCGCATGCTCGGGGGAGGAGAGGACCCACTCTACGTGGCACGGA A G WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2783449..2783550 32194978 MeRIP-seq:(Medium) rs1411128154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841753,Human_RBP_ID_8905045,Human_RBP_ID_9309471 Human_Splice_Rec_733312,Human_Splice_Rec_733313,Human_Splice_Rec_733324,Human_Splice_Rec_733325,Human_Splice_Rec_733336,Human_Splice_Rec_733337,Human_Splice_Rec_733348,Human_Splice_Rec_733349,Human_Splice_Rec_733358,Human_Splice_Rec_733359 RMVar_hsa_circ_13644,RMVar_hsa_circ_283108,RMVar_hsa_circ_365013,RMVar_hsa_circ_236901,RMVar_hsa_circ_125205,RMVar_hsa_circ_289201,RMVar_hsa_circ_277934,RMVar_hsa_circ_236902,RMVar_hsa_circ_236900 58624 RMVar_ID_58624 Human_SNP_ID_264780972 m1A Human chr6 - 2833875 2833875 2833875 AGTTACACTCTCAACTCCGACCTCGCCCGCCTAGGTGTGCAGGATCTCTTTAACAGTAGCAAGGC AGTTACACTCTCAACTCCGACCTCGCCCGCCTGGGTGTGCAGGATCTCTTTAACAGTAGCAAGGC T C SERPINB1 Ensembl:ENSG00000021355 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2833528..2833879 32194978 MeRIP-seq:(Medium) rs772390994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660109,Human_RBP_ID_17421439,Human_RBP_ID_22772573 RMVar_hsa_circ_106164,RMVar_hsa_circ_109378,RMVar_hsa_circ_236903,RMVar_hsa_circ_236904 58625 RMVar_ID_58625 Human_SNP_ID_264782643 m1A Human chr6 - 2840574 2840574 2840574 TCTGTGTTGCAGTTTTCACCATGGAGCAGCTGAGCTCAGCAAACACCCGCTTCGCCTTGGACCTG TCTGTGTTGCAGTTTTCACCATGGAGCAGCTGGGCTCAGCAAACACCCGCTTCGCCTTGGACCTG T C SERPINB1 Ensembl:ENSG00000021355 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2840465..2841386 32194978 MeRIP-seq:(Medium) rs1309836175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903629,Human_RBP_ID_9335898 Human_Splice_Rec_733364,Human_Splice_Rec_733392,Human_Splice_Rec_733400 RMVar_hsa_circ_21050,RMVar_hsa_circ_106164,RMVar_hsa_circ_113888,RMVar_hsa_circ_236904,RMVar_hsa_circ_354656,RMVar_hsa_circ_236906,RMVar_hsa_circ_310046,RMVar_hsa_circ_81654,RMVar_hsa_circ_90541,RMVar_hsa_circ_114731,RMVar_hsa_circ_236908,RMVar_hsa_circ_266264,RMVar_hsa_circ_236909,RMVar_hsa_circ_236910 58626 RMVar_ID_58626 Human_SNP_ID_264782941 m1A Human chr6 - 2841717 2841717 2841717 CTCAGCTTCCAGCCCGGCACCCCCCACCCCCCAGGCTCAGGCCCCTCAGACCCGCAGCTCCCTGC CTCAGCTTCCAGCCCGGCACCCCCCACCCCCCCGGCTCAGGCCCCTCAGACCCGCAGCTCCCTGC T G SERPINB1 Ensembl:ENSG00000021355 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:2841712..2841855 26863196 MeRIP-seq:(Medium) rs1481753668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113888,RMVar_hsa_circ_236906,RMVar_hsa_circ_81654,RMVar_hsa_circ_90541,RMVar_hsa_circ_114731,RMVar_hsa_circ_236908,RMVar_hsa_circ_236909,RMVar_hsa_circ_236910 58627 RMVar_ID_58627 Human_SNP_ID_264782946 m1A Human chr6 - 2841724 2841724 2841724 TCCCTCGCTCAGCTTCCAGCCCGGCACCCCCCACCCCCCAGGCTCAGGCCCCTCAGACCCGCAGC TCCCTCGCTCAGCTTCCAGCCCGGCACCCCCCCCCCCCCAGGCTCAGGCCCCTCAGACCCGCAGC T G SERPINB1 Ensembl:ENSG00000021355 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:2841717..2841809 26863196 MeRIP-seq:(Medium) rs887518736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113888,RMVar_hsa_circ_236906,RMVar_hsa_circ_81654,RMVar_hsa_circ_90541,RMVar_hsa_circ_114731,RMVar_hsa_circ_236908,RMVar_hsa_circ_236909,RMVar_hsa_circ_236910 58628 RMVar_ID_58628 Human_SNP_ID_264786057 m1A Human chr6 + 2853466 2853466 2853466 TCCTGGGACCCCCTCGCCTTTCCCTGACCCTCACCTGAAGTCCCCTCCCCTTTCCCTGACCCTCT TCCTGGGACCCCCTCGCCTTTCCCTGACCCTCCCCTGAAGTCCCCTCCCCTTTCCCTGACCCTCT A C HSALNG0047515 RNACentral:URS0000E9F536 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:2853416..2853603 26863196 MeRIP-seq:(Medium) rs575716787 Functional Loss SNV dbSNP153 33..33 33 - - - 58629 RMVar_ID_58629 Human_SNP_ID_264786058 m1A Human chr6 + 2853466 2853466 2853466 TCCTGGGACCCCCTCGCCTTTCCCTGACCCTCACCTGAAGTCCCCTCCCCTTTCCCTGACCCTCT TCCTGGGACCCCCTCGCCTTTCCCTGACCCTCTCCTGAAGTCCCCTCCCCTTTCCCTGACCCTCT A T HSALNG0047515 RNACentral:URS0000E9F536 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:2853416..2853603 26863196 MeRIP-seq:(Medium) rs575716787 Functional Loss SNV dbSNP153 33..33 33 - - - 58630 RMVar_ID_58630 Human_SNP_ID_264786581 m1A Human chr6 - 2855442 2855442 2855442 GTGCGCTAGCCCTTCATGGAGGTCAGAGAGGAAGAAACAAAGGCAGCTGTGGCCTCGGCGGTCAC GTGCGCTAGCCCTTCATGGAGGTCAGAGAGGAGGAAACAAAGGCAGCTGTGGCCTCGGCGGTCAC T C SERPINB9P1 Ensembl:ENSG00000230438 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:2855391..2855459 26863196 MeRIP-seq:(Medium) rs1036605299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5619927 58631 RMVar_ID_58631 Human_SNP_ID_264821993 m1A Human chr6 - 2971027 2971027 2971027 GACGCGTGCTCAGTCTTGGGGCGCCGGGTGTTAGGAGCCGGGCGGGAGGCGGAGAGAGGCCGAGG GACGCGTGCTCAGTCTTGGGGCGCCGGGTGTTGGGAGCCGGGCGGGAGGCGGAGAGAGGCCGAGG T C SERPINB6 Ensembl:ENSG00000124570 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:2971024..2971192 32194978 MeRIP-seq:(Medium) rs6938590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1217025,Human_RBP_ID_17161214 GWAS_ID_6862,GWAS_ID_6863 RMVar_hsa_circ_83951,RMVar_hsa_circ_236920 58632 RMVar_ID_58632 Human_SNP_ID_264822072 m1A Human chr6 + 2971333 2971333 2971333 CGGACGCTCGCCCGGGCCCCCGCCCCGCTGGGACTGCTGGGGTCACAGCCCCGCGCGGCCACGCC CGGACGCTCGCCCGGGCCCCCGCCCCGCTGGGGCTGCTGGGGTCACAGCCCCGCGCGGCCACGCC A G NONHSAG042719.2 RNACentral:URS00009BF6B0 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:2971321..2971420 26863196 MeRIP-seq:(Medium) rs558121313 Functional Loss SNV dbSNP153 33..33 33 - - - 58633 RMVar_ID_58633 Human_SNP_ID_264831181 m1A Human chr6 - 3006518 3006518 3006518 CGTAAGAAGGTGGATTCCTTCTCTCTGATTTGATGGGTGGCTGGGGCTTTCCTGCGTAGTCTCTC CGTAAGAAGGTGGATTCCTTCTCTCTGATTTGGTGGGTGGCTGGGGCTTTCCTGCGTAGTCTCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:3006421..3006602 26863196 MeRIP-seq:(Medium) rs953973323 Functional Loss SNV dbSNP153 33..33 33 - - - 58634 RMVar_ID_58634 Human_SNP_ID_264831200 m1A Human chr6 - 3006561 3006561 3006561 AAAAAAGTCTTACTCCACAATAGTGAATCATTACCTGCCATAGCGTAAGAAGGTGGATTCCTTCT AAAAAAGTCTTACTCCACAATAGTGAATCATTCCCTGCCATAGCGTAAGAAGGTGGATTCCTTCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:3006526..3006575 26863196 MeRIP-seq:(Medium) rs762221263 Functional Loss SNV dbSNP153 33..33 33 - - - 58635 RMVar_ID_58635 Human_SNP_ID_264834682 m1A Human chr6 - 3019548 3019548 3019548 CGCAGCCACCATCCCCTTTCTTTCTTCTTCGGATGCAATTTCAGGAGCAAAGCTGATCTGAGGGG CGCAGCCACCATCCCCTTTCTTTCTTCTTCGGTTGCAATTTCAGGAGCAAAGCTGATCTGAGGGG T A lnc-SERPINB6-1,lnc-SERPINB6-1:2 RNACentral:URS00008BF125,RNACentral:URS00008BE890 lincRNA,lincRNA exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:3019476..3019550 32194978 MeRIP-seq:(Medium) rs774654286 Functional Loss SNV dbSNP153 33..33 33 - - - 58636 RMVar_ID_58636 Human_SNP_ID_264846502 m1A Human chr6 + 3064015 3064015 3064015 CGCAGCAGCAGGGCCCGGTCCTGCGCCTCGGGAGTCGGCGTCCAGGCTCGGAGCGCGACACGGAG CGCAGCAGCAGGGCCCGGTCCTGCGCCTCGGGGGTCGGCGTCCAGGCTCGGAGCGCGACACGGAG A G RIPK1 Ensembl:ENSG00000137275 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3063969..3064111 26863196 MeRIP-seq:(Medium) rs12203636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_733791 58637 RMVar_ID_58637 Human_SNP_ID_264846580 m1A Human chr6 - 3064225 3064225 3064225 CGGAGGCGGAAACCGGCTGCGCGCTGCAGGGGACCCCCCACAGACCGTTGCTGACCCCGCCGAGA CGGAGGCGGAAACCGGCTGCGCGCTGCAGGGGCCCCCCCACAGACCGTTGCTGACCCCGCCGAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3064195..3064260 26863196 MeRIP-seq:(Medium) rs918080549 Functional Loss SNV dbSNP153 33..33 33 - - - 58638 RMVar_ID_58638 Human_SNP_ID_264847938 m1A Human chr6 - 3068576 3068576 3068576 GCCCCGCCCGGATGGCCGCGCTCTGGCGCCCCAGCTGTGGGTCCCCTGGAGTCGCCGCGCTCCGG GCCCCGCCCGGATGGCCGCGCTCTGGCGCCCCTGCTGTGGGTCCCCTGGAGTCGCCGCGCTCCGG T A AL031963.3 Ensembl:ENSG00000272277 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3068530..3068652 26863196 MeRIP-seq:(Medium) rs935063901 Functional Loss SNV dbSNP153 33..33 33 - - - 58639 RMVar_ID_58639 Human_SNP_ID_264850436 m1A Human chr6 - 3076725 3076725 3076725 AGAAAACAGAGAGAAAACCTCAGGGCAAGACTATATATATATATATATATATATATATGTTTTTT AGAAAACAGAGAGAAAACCTCAGGGCAAGACTCTATATATATATATATATATATATATGTTTTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3076722..3076866 26863196 MeRIP-seq:(Medium) rs1003371350 Functional Loss SNV dbSNP153 33..33 33 - - - 58640 RMVar_ID_58640 Human_SNP_ID_264864687 m1A Human chr6 + 3132239 3132239 3132239 CGCACCTCCTCTTGGCTCCTTGGTCATTCTGCAGCGTTTGAGAACATGCTCATGATGTGTGCGCC CGCACCTCCTCTTGGCTCCTTGGTCATTCTGCGGCGTTTGAGAACATGCTCATGATGTGTGCGCC A G BPHL Ensembl:ENSG00000137274 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:3132107..3132336 26863196 MeRIP-seq:(Medium) rs1210858555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21323528,Human_RBP_ID_23244933 RMVar_hsa_circ_338994,RMVar_hsa_circ_21265,RMVar_hsa_circ_357032 58641 RMVar_ID_58641 Human_SNP_ID_264868289 m1A Human chr6 - 3145615 3145527 3145616 CGAACCAGCACTCCAACCCGAACCAGCACTCGACCCAAACCAGCACTCCGACCCAAACCAGCACT CGAACCAGCACTCCAACCCGAACCAGCACTC__________________________________ GGAGTGCTGGTTCCGGTTGGAGTGCTGGTGTGGGTTGGAGTGCTGGTGTGGGTCGGAGTGCTGGTTTGGGTCGGAGTGCTGGTTTGGGTC G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3144998..3145795 26863196 MeRIP-seq:(Medium) rs1561800092 Functional Loss DEL dbSNP153 32..65 33 - - - 58642 RMVar_ID_58642 Human_SNP_ID_264868328 m1A Human chr6 - 3145593 3145593 3145593 CCAGCACTCGACCCAAACCAGCACTCCGACCCAAACCAGCACTCCGACCCACACCAGCACTCCAA CCAGCACTCGACCCAAACCAGCACTCCGACCCGAACCAGCACTCCGACCCACACCAGCACTCCAA T C AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:3145587..3145671 26863196 MeRIP-seq:(Medium) rs1380111686 Functional Loss SNV dbSNP153 33..33 33 - - - 58643 RMVar_ID_58643 Human_SNP_ID_264868340 m1A Human chr6 - 3145615 3145612 3145616 CGAACCAGCACTCCAACCCGAACCAGCACTCGACCCAAACCAGCACTCCGACCCAAACCAGCACT CGAACCAGCACTCCAACCCGAACCAGCACTC____CAAACCAGCACTCCGACCCAAACCAGCACT GGGTC G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3144998..3145795 26863196 MeRIP-seq:(Medium) rs199752886 Functional Loss DEL dbSNP153 32..35 33 - - - 58644 RMVar_ID_58644 Human_SNP_ID_264868761 m1A Human chr6 - 3146361 3146361 3146361 CAAATCAGCACTCAACTGGAACCAGCACTCCAACCCACACCAGCACTCCACCCCGAACCAGCACT CAAATCAGCACTCAACTGGAACCAGCACTCCACCCCACACCAGCACTCCACCCCGAACCAGCACT T G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:3146261..3146407 26863196 MeRIP-seq:(Medium) rs1273741824 Functional Loss SNV dbSNP153 33..33 33 - - - 58645 RMVar_ID_58645 Human_SNP_ID_264869023 m1A Human chr6 - 3146794 3146794 3146794 GAACCAGCACTCCAACCCGAACCAGCACTCCGACCCAAACCAGCACTCGACCCAAACCAGCACTC GAACCAGCACTCCAACCCGAACCAGCACTCCGCCCCAAACCAGCACTCGACCCAAACCAGCACTC T G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3146776..3146911 26863196 MeRIP-seq:(Medium) rs1315810451 Functional Loss SNV dbSNP153 33..33 33 - - - 58646 RMVar_ID_58646 Human_SNP_ID_264869066 m1A Human chr6 - 3146866 3146865 3146866 CCGAACCAGCACTCGCCCAAACCAGCACTCCGACCCAAACCAGCACTCCGACCCAAACCAGCACT CCGAACCAGCACTCGCCCAAACCAGCACTCCG_CCCAAACCAGCACTCCGACCCAAACCAGCACT GT G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3146754..3146914 26863196 MeRIP-seq:(Medium) rs1166161192 Functional Loss DEL dbSNP153 33..33 33 - - - 58647 RMVar_ID_58647 Human_SNP_ID_264869067 m1A Human chr6 - 3146866 3146866 3146866 CCGAACCAGCACTCGCCCAAACCAGCACTCCGACCCAAACCAGCACTCCGACCCAAACCAGCACT CCGAACCAGCACTCGCCCAAACCAGCACTCCGCCCCAAACCAGCACTCCGACCCAAACCAGCACT T G AL031963.1 Ensembl:ENSG00000228170 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3146754..3146914 26863196 MeRIP-seq:(Medium) rs1227686193 Functional Loss SNV dbSNP153 33..33 33 - - - 58648 RMVar_ID_58648 Human_SNP_ID_264888474 m1A Human chr6 - 3222071 3222068 3222071 TGGTGGTGGTGGTAGTGATGGTGATGATGGTGATAGTGGTGATTGTGATGGTGGTGGTGGTAGTA TGGTGGTGGTGGTAGTGATGGTGATGATGGTG___GTGGTGATTGTGATGGTGGTGGTGGTAGTA CTAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3222062..3222127 26863196 MeRIP-seq:(Medium) rs1359991123 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_236953 58649 RMVar_ID_58649 Human_SNP_ID_264888477 m1A Human chr6 - 3222071 3222069 3222072 TGGTGGTGGTGGTAGTGATGGTGATGATGGTGATAGTGGTGATTGTGATGGTGGTGGTGGTAGTA TGGTGGTGGTGGTAGTGATGGTGATGATGGT___AGTGGTGATTGTGATGGTGGTGGTGGTAGTA TATC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3222062..3222127 26863196 MeRIP-seq:(Medium) rs1561824858 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_236953 58650 RMVar_ID_58650 Human_SNP_ID_264888480 m1A Human chr6 - 3222071 3222071 3222071 TGGTGGTGGTGGTAGTGATGGTGATGATGGTGATAGTGGTGATTGTGATGGTGGTGGTGGTAGTA TGGTGGTGGTGGTAGTGATGGTGATGATGGTGGTAGTGGTGATTGTGATGGTGGTGGTGGTAGTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3222062..3222127 26863196 MeRIP-seq:(Medium) rs375849666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236953 58651 RMVar_ID_58651 Human_SNP_ID_264900843 m1A Human chr6 - 3259059 3259059 3259059 CTCCCACAGCCTCGCGCTGAAGTTGTGCAGGGAGACGTCCCCGCCGGCGGCGACAACCAGCCCCT CTCCCACAGCCTCGCGCTGAAGTTGTGCAGGGGGACGTCCCCGCCGGCGGCGACAACCAGCCCCT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:3258964..3259092 26863196 MeRIP-seq:(Medium) rs1257226067 Functional Loss SNV dbSNP153 33..33 33 - - - 58652 RMVar_ID_58652 Human_SNP_ID_264900861 m1A Human chr6 + 3259093 3259093 3259093 CCTGCACAACTTCAGCGCGAGGCTGTGGGAGCAGCTGGTCCACTTCCACGTCATGCGGCTGACGG CCTGCACAACTTCAGCGCGAGGCTGTGGGAGCGGCTGGTCCACTTCCACGTCATGCGGCTGACGG A G PSMG4 Ensembl:ENSG00000180822 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:3258976..3259276 26863196 MeRIP-seq:(Medium) rs1201680330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662135,Human_RBP_ID_1671398,Human_RBP_ID_4903643,Human_RBP_ID_9335908,Human_RBP_ID_15789642,Human_RBP_ID_17161218,Human_RBP_ID_18502463,Human_RBP_ID_27345932 RMVar_hsa_circ_115216,RMVar_hsa_circ_236955 58653 RMVar_ID_58653 Human_SNP_ID_264900862 m1A Human chr6 + 3259093 3259093 3259093 CCTGCACAACTTCAGCGCGAGGCTGTGGGAGCAGCTGGTCCACTTCCACGTCATGCGGCTGACGG CCTGCACAACTTCAGCGCGAGGCTGTGGGAGCTGCTGGTCCACTTCCACGTCATGCGGCTGACGG A T PSMG4 Ensembl:ENSG00000180822 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:3258976..3259276 26863196 MeRIP-seq:(Medium) rs1201680330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662135,Human_RBP_ID_1671398,Human_RBP_ID_4903643,Human_RBP_ID_9335908,Human_RBP_ID_15789642,Human_RBP_ID_17161218,Human_RBP_ID_18502463,Human_RBP_ID_27345932 RMVar_hsa_circ_115216,RMVar_hsa_circ_236955 58654 RMVar_ID_58654 Human_SNP_ID_264905104 m1A Human chr6 + 3270442 3270442 3270442 ACAGGGAAGTGTTGCTGCTCTGGCAACATTTCATAAAGGTGTTGCTCAACAGCTTCAGGTATCCC ACAGGGAAGTGTTGCTGCTCTGGCAACATTTCGTAAAGGTGTTGCTCAACAGCTTCAGGTATCCC A G PSMG4 Ensembl:ENSG00000180822 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:3270391..3270542 32194978 MeRIP-seq:(Medium) rs146550014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27096562 58655 RMVar_ID_58655 Human_SNP_ID_264952529 m1A Human chr6 - 3456948 3456948 3456948 GAGCAGCAGCCTTTGCCCGCACCGCCGCCCGCAGGGCCCTGAACCGCCGGCAAGGGCGCGGGCCG GAGCAGCAGCCTTTGCCCGCACCGCCGCCCGCCGGGCCCTGAACCGCCGGCAAGGGCGCGGGCCG T G SLC22A23 Ensembl:ENSG00000137266 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:3456901..3457085 26863196 MeRIP-seq:(Medium) rs1244844869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903075,Human_RBP_ID_5532271,Human_RBP_ID_8730292,Human_RBP_ID_22460867 58656 RMVar_ID_58656 Human_SNP_ID_265025135 m1A Human chr6 + 3723586 3723586 3723586 AGCACAGTGGACAGCATCAGAGCTGGCAGTGAACAGCTGAGGCGGGGGAGGCCTGATAGAGAGGT AGCACAGTGGACAGCATCAGAGCTGGCAGTGAGCAGCTGAGGCGGGGGAGGCCTGATAGAGAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:3723536..3723690 26863196 MeRIP-seq:(Medium) rs776604366 Functional Loss SNV dbSNP153 33..33 33 - - - 58657 RMVar_ID_58657 Human_SNP_ID_265025146 m1A Human chr6 + 3723602 3723602 3723602 TCAGAGCTGGCAGTGAACAGCTGAGGCGGGGGAGGCCTGATAGAGAGGTTCAGTCCCAAATGTCT TCAGAGCTGGCAGTGAACAGCTGAGGCGGGGGTGGCCTGATAGAGAGGTTCAGTCCCAAATGTCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:3723551..3723695 26863196 MeRIP-seq:(Medium) rs201329088 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 58658 RMVar_ID_58658 Human_SNP_ID_265026007 m1A Human chr6 + 3726555 3726555 3726555 GCCAGTCCCACAAGCCTGACAGGGACCCCCCCATGCTCAGTCATGGAGCAGGGATTCAGCAGAGG GCCAGTCCCACAAGCCTGACAGGGACCCCCCCCTGCTCAGTCATGGAGCAGGGATTCAGCAGAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:3726541..3726641 32194978 MeRIP-seq:(Medium) rs948939760 Functional Loss SNV dbSNP153 33..33 33 - - - 58659 RMVar_ID_58659 Human_SNP_ID_265026913 m1A Human chr6 + 3730181 3730181 3730181 AGGGACTTCGCTTAGACTCTCACATTTCACTAAAGATGGTCCCTGAGAAGCTCCGGTTCCCTCCT AGGGACTTCGCTTAGACTCTCACATTTCACTACAGATGGTCCCTGAGAAGCTCCGGTTCCCTCCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:3730176..3730279 32194978 MeRIP-seq:(Medium) rs928417302 Functional Loss SNV dbSNP153 33..33 33 - - - 58660 RMVar_ID_58660 Human_SNP_ID_265032257 m1A Human chr6 - 3750554 3750554 3750554 CGGTGGCTTCCCTTTTCCTACCGCTCTGCCCGATCTTTCTTTTGGAGGCCAGGCTGAGGGGGTGG CGGTGGCTTCCCTTTTCCTACCGCTCTGCCCGGTCTTTCTTTTGGAGGCCAGGCTGAGGGGGTGG T C PXDC1 Ensembl:ENSG00000168994 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:3750551..3751107 26863196 MeRIP-seq:(Medium) rs1033195098 Functional Loss SNV dbSNP153 33..33 33 - - - 58661 RMVar_ID_58661 Human_SNP_ID_265032258 m1A Human chr6 - 3750554 3750554 3750554 CGGTGGCTTCCCTTTTCCTACCGCTCTGCCCGATCTTTCTTTTGGAGGCCAGGCTGAGGGGGTGG CGGTGGCTTCCCTTTTCCTACCGCTCTGCCCGCTCTTTCTTTTGGAGGCCAGGCTGAGGGGGTGG T G PXDC1 Ensembl:ENSG00000168994 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:3750551..3751107 26863196 MeRIP-seq:(Medium) rs1033195098 Functional Loss SNV dbSNP153 33..33 33 - - - 58662 RMVar_ID_58662 Human_SNP_ID_265032607 m1A Human chr6 - 3751356 3751356 3751356 CAGCGTGCTCTACCTGCACCGCAGCCTGGCGGACCTGGGCCGCCTGTGGCAGCGCCTGCGCGACG CAGCGTGCTCTACCTGCACCGCAGCCTGGCGGCCCTGGGCCGCCTGTGGCAGCGCCTGCGCGACG T G PXDC1 Ensembl:ENSG00000168994 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:3751307..3751505 32194978 MeRIP-seq:(Medium) rs1356598642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_734403,Human_Splice_Rec_734411,Human_Splice_Rec_734427 58663 RMVar_ID_58663 Human_SNP_ID_265032775 m1A Human chr6 - 3751626 3751599 3751626 GAGTGACGGGCCGACCCCGGACGACCCCGGCCACGGACAGACCCGGGACGACCCCGGCCGGGGCG GAGTGACGGGCCGACCCCGGACGACCCCGGCC___________________________GGGGCG CGGCCGGGGTCGTCCCGGGTCTGTCCGT C PXDC1 Ensembl:ENSG00000168994 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:3750499..3751985 26863196 MeRIP-seq:(Medium) rs955976969 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_4903078 58664 RMVar_ID_58664 Human_SNP_ID_265032976 m1A Human chr6 - 3751976 3751976 3751976 ACCGACCTGCGGCTCCGGGGCCGCGAGGGAGGAGGCGCGGGGGGCGCGAGGCGGGGGCGAGCGCT ACCGACCTGCGGCTCCGGGGCCGCGAGGGAGGGGGCGCGGGGGGCGCGAGGCGGGGGCGAGCGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:3751926..3752026 26863196 MeRIP-seq:(Medium) rs1292185475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904448 58665 RMVar_ID_58665 Human_SNP_ID_265049518 m1A Human chr6 + 3804565 3804565 3804565 TGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCCCGCCATTCTCCT TGGAGTGCAGTGGCGCGATCTCAGCTCACTGCCAGCTCCGCCTCCCGGGTTCCCGCCATTCTCCT A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:3804546..3804630 26863410 MeRIP-seq:(Medium) rs916925756 Functional Loss SNV dbSNP153 33..33 33 - - - 58666 RMVar_ID_58666 Human_SNP_ID_265105253 m1A Human chr6 + 4031610 4031610 4031610 GAAAAGAGTATAAATGAAGAAAATGGAGAAGTATCAGAAGACCAGTCTCAAAATAAGCACAGTCG GAAAAGAGTATAAATGAAGAAAATGGAGAAGTCTCAGAAGACCAGTCTCAAAATAAGCACAGTCG A C PRPF4B Ensembl:ENSG00000112739 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:4031550..4031853 26863196 MeRIP-seq:(Medium) rs190419800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949009,Human_RBP_ID_2021044,Human_RBP_ID_3007446,Human_RBP_ID_3969497,Human_RBP_ID_5532276,Human_RBP_ID_7605592,Human_RBP_ID_9399831,Human_RBP_ID_15823520,Human_RBP_ID_24162563,Human_RBP_ID_24548526,Human_RBP_ID_26353315,Human_RBP_ID_27828203 Human_Splice_Rec_734452,Human_Splice_Rec_734482 Human_miRNA_ID_3085694 RMVar_hsa_circ_58849,RMVar_hsa_circ_111498,RMVar_hsa_circ_236967,RMVar_hsa_circ_102759,RMVar_hsa_circ_236968,RMVar_hsa_circ_326913,RMVar_hsa_circ_358863,RMVar_hsa_circ_121680,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 58667 RMVar_ID_58667 Human_SNP_ID_265105254 m1A Human chr6 + 4031610 4031610 4031610 GAAAAGAGTATAAATGAAGAAAATGGAGAAGTATCAGAAGACCAGTCTCAAAATAAGCACAGTCG GAAAAGAGTATAAATGAAGAAAATGGAGAAGTTTCAGAAGACCAGTCTCAAAATAAGCACAGTCG A T PRPF4B Ensembl:ENSG00000112739 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:4031550..4031853 26863196 MeRIP-seq:(Medium) rs190419800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949009,Human_RBP_ID_2021044,Human_RBP_ID_3007446,Human_RBP_ID_3969497,Human_RBP_ID_5532276,Human_RBP_ID_7605592,Human_RBP_ID_9399831,Human_RBP_ID_15823520,Human_RBP_ID_24162563,Human_RBP_ID_24548526,Human_RBP_ID_26353315,Human_RBP_ID_27828203 Human_Splice_Rec_734452,Human_Splice_Rec_734482 Human_miRNA_ID_3085694 RMVar_hsa_circ_58849,RMVar_hsa_circ_111498,RMVar_hsa_circ_236967,RMVar_hsa_circ_102759,RMVar_hsa_circ_236968,RMVar_hsa_circ_326913,RMVar_hsa_circ_358863,RMVar_hsa_circ_121680,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 58668 RMVar_ID_58668 Human_SNP_ID_265105264 m1A Human chr6 + 4031636 4031636 4031636 AGAAGTATCAGAAGACCAGTCTCAAAATAAGCACAGTCGTCACAAAAAAAAGAAGCATAAACACA AGAAGTATCAGAAGACCAGTCTCAAAATAAGCCCAGTCGTCACAAAAAAAAGAAGCATAAACACA A C PRPF4B Ensembl:ENSG00000112739 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:4021339..4031757 26863196 MeRIP-seq:(Medium) rs757401402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949009,Human_RBP_ID_2021044,Human_RBP_ID_3007446,Human_RBP_ID_3969497,Human_RBP_ID_5532276,Human_RBP_ID_5617921,Human_RBP_ID_9399831,Human_RBP_ID_24548526,Human_RBP_ID_26353315,Human_RBP_ID_27098021,Human_RBP_ID_27828203 Human_Splice_Rec_734452,Human_Splice_Rec_734482 Human_miRNA_ID_626245,Human_miRNA_ID_2236504,Human_miRNA_ID_3066928 RMVar_hsa_circ_58849,RMVar_hsa_circ_111498,RMVar_hsa_circ_236967,RMVar_hsa_circ_102759,RMVar_hsa_circ_236968,RMVar_hsa_circ_326913,RMVar_hsa_circ_358863,RMVar_hsa_circ_121680,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 58669 RMVar_ID_58669 Human_SNP_ID_265105348 m1A Human chr6 + 4031965 4031965 4031965 GTTATGAGTCTGGCTCTGAAGAAGAGGGGGAAATTCATGAAAAGGCAAGAAATGGAAATAGGTCT GTTATGAGTCTGGCTCTGAAGAAGAGGGGGAAGTTCATGAAAAGGCAAGAAATGGAAATAGGTCT A G PRPF4B Ensembl:ENSG00000112739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:4031855..4032055 32194978 MeRIP-seq:(Medium) rs1297667033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79827,Human_RBP_ID_214809,Human_RBP_ID_251367,Human_RBP_ID_789529,Human_RBP_ID_841616,Human_RBP_ID_951616,Human_RBP_ID_2021051,Human_RBP_ID_3007454,Human_RBP_ID_5532277,Human_RBP_ID_7605598,Human_RBP_ID_8237292,Human_RBP_ID_9399832,Human_RBP_ID_15823523,Human_RBP_ID_17663195,Human_RBP_ID_18413808,Human_RBP_ID_18865537,Human_RBP_ID_22104545,Human_RBP_ID_22312706,Human_RBP_ID_24548316,Human_RBP_ID_24554586,Human_RBP_ID_26353316,Human_RBP_ID_27827221 RMVar_hsa_circ_58849,RMVar_hsa_circ_111498,RMVar_hsa_circ_236967,RMVar_hsa_circ_102759,RMVar_hsa_circ_236968,RMVar_hsa_circ_326913,RMVar_hsa_circ_358863,RMVar_hsa_circ_121680,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 58670 RMVar_ID_58670 Human_SNP_ID_265105495 m1A Human chr6 - 4032404 4032404 4032404 ACCTTCTGTCTTTGGATTTACCTCTTAAATCAACTGGGGATCTGGATTTTTTACCTCGATCGCGA ACCTTCTGTCTTTGGATTTACCTCTTAAATCACCTGGGGATCTGGATTTTTTACCTCGATCGCGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:4032353..4032602 32194978 MeRIP-seq:(Medium) rs1473082771 Functional Loss SNV dbSNP153 33..33 33 - - - 58671 RMVar_ID_58671 Human_SNP_ID_265129498 m1A Human chr6 + 4127830 4127830 4127830 CAGCTTTAAGTGCACGCATAATTTCATGATACATCTGTGTAATGGGAAGACAAGGAAAAGAAAAG CAGCTTTAAGTGCACGCATAATTTCATGATACTTCTGTGTAATGGGAAGACAAGGAAAAGAAAAG A T C6orf201 Ensembl:ENSG00000185689 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:4126125..4130245 32194978 MeRIP-seq:(Medium) rs878941184 Functional Loss SNV dbSNP153 33..33 33 - - - 58672 RMVar_ID_58672 Human_SNP_ID_265130904 m1A Human chr6 - 4133684 4133684 4133684 TGTAGTTCTCTGCAGGTCACTAGTTTCCCGGTAGTTCAGCTGCACATGAATAGAACAGCAATGAG TGTAGTTCTCTGCAGGTCACTAGTTTCCCGGTCGTTCAGCTGCACATGAATAGAACAGCAATGAG T G ECI2 Ensembl:ENSG00000198721 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:4133585..4133725 26863196 MeRIP-seq:(Medium) rs770734736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664426,Human_RBP_ID_792289,Human_RBP_ID_2021257,Human_RBP_ID_4903645,Human_RBP_ID_15825545 Human_Splice_Rec_734736,Human_Splice_Rec_734754,Human_Splice_Rec_734772,Human_Splice_Rec_734792,Human_Splice_Rec_734810,Human_Splice_Rec_734824,Human_Splice_Rec_734840,Human_Splice_Rec_734858,Human_Splice_Rec_734888,Human_Splice_Rec_734896 RMVar_hsa_circ_69854,RMVar_hsa_circ_69893 58673 RMVar_ID_58673 Human_SNP_ID_265205858 m1A Human chr6 + 4427973 4427973 4427973 CCATCTGGCCTTTTCCAGCCACGTCTACGGCCATACCACCCTGAACGCCCCCGATCTCGTCTGAT CCATCTGGCCTTTTCCAGCCACGTCTACGGCCTTACCACCCTGAACGCCCCCGATCTCGTCTGAT A T RNA5SP202 Ensembl:ENSG00000201185 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs962380287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270871,Human_RBP_ID_1218055,Human_RBP_ID_1674150,Human_RBP_ID_4914548,Human_RBP_ID_5216370,Human_RBP_ID_5268982,Human_RBP_ID_5451310,Human_RBP_ID_5511790,Human_RBP_ID_5617988,Human_RBP_ID_8271674,Human_RBP_ID_8901859,Human_RBP_ID_10286334,Human_RBP_ID_15836762,Human_RBP_ID_17065060,Human_RBP_ID_17710951,Human_RBP_ID_18202532,Human_RBP_ID_18211404,Human_RBP_ID_18519310,Human_RBP_ID_18539913,Human_RBP_ID_21347267,Human_RBP_ID_21947189,Human_RBP_ID_22832808,Human_RBP_ID_23116604,Human_RBP_ID_23120451,Human_RBP_ID_23139071,Human_RBP_ID_23314773,Human_RBP_ID_26537149,Human_RBP_ID_26751393,Human_RBP_ID_27102603,Human_RBP_ID_27347994,Human_RBP_ID_27525286 58674 RMVar_ID_58674 Human_SNP_ID_265293767 m1A Human chr6 - 4776385 4776356 4776386 TCCTACTTGCGACCAAAAAACCTGCCCCGGCTACTGAGCATGCCCAGTGCGGCCGCCCGGCCCTG TCCTACTTGCGACCAAAAAACCTGCCCCGGC______________________________CCTG GGCCGGGCGGCCGCACTGGGCATGCTCAGTA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:4776342..4776504 26863196 MeRIP-seq:(Medium) rs1364932764 Functional Loss DEL dbSNP153 32..61 33 - - - 58675 RMVar_ID_58675 Human_SNP_ID_265293774 m1A Human chr6 - 4776385 4776385 4776385 TCCTACTTGCGACCAAAAAACCTGCCCCGGCTACTGAGCATGCCCAGTGCGGCCGCCCGGCCCTG TCCTACTTGCGACCAAAAAACCTGCCCCGGCTGCTGAGCATGCCCAGTGCGGCCGCCCGGCCCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:4776342..4776504 26863196 MeRIP-seq:(Medium) rs1165396591 Functional Loss SNV dbSNP153 33..33 33 - - - 58676 RMVar_ID_58676 Human_SNP_ID_265293814 m1A Human chr6 + 4776521 4776521 4776521 CAGCCCGCCCGGCCCCGCGGCGGGGCGCGATGAGCCCGAGCGCGAGCCGGCCCGCCGGGGAGTGA CAGCCCGCCCGGCCCCGCGGCGGGGCGCGATGCGCCCGAGCGCGAGCCGGCCCGCCGGGGAGTGA A C CDYL Ensembl:ENSG00000153046 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr6:4776401..4776716;chr6:4776426..4776550 26863410 MeRIP-seq:(Medium) rs1291474067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903647,Human_RBP_ID_8905619,Human_RBP_ID_9401505,Human_RBP_ID_22534048,Human_RBP_ID_27828225 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 58677 RMVar_ID_58677 Human_SNP_ID_265293815 m1A Human chr6 + 4776521 4776521 4776521 CAGCCCGCCCGGCCCCGCGGCGGGGCGCGATGAGCCCGAGCGCGAGCCGGCCCGCCGGGGAGTGA CAGCCCGCCCGGCCCCGCGGCGGGGCGCGATGTGCCCGAGCGCGAGCCGGCCCGCCGGGGAGTGA A T CDYL Ensembl:ENSG00000153046 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr6:4776401..4776716;chr6:4776426..4776550 26863410 MeRIP-seq:(Medium) rs1291474067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903647,Human_RBP_ID_8905619,Human_RBP_ID_9401505,Human_RBP_ID_22534048,Human_RBP_ID_27828225 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 58678 RMVar_ID_58678 Human_SNP_ID_265293821 m1A Human chr6 + 4776527 4776527 4776527 GCCCGGCCCCGCGGCGGGGCGCGATGAGCCCGAGCGCGAGCCGGCCCGCCGGGGAGTGAGCGCGG GCCCGGCCCCGCGGCGGGGCGCGATGAGCCCGTGCGCGAGCCGGCCCGCCGGGGAGTGAGCGCGG A T CDYL Ensembl:ENSG00000153046 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:4776455..4776543 26863410 MeRIP-seq:(Medium) rs1392850257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4893162,Human_RBP_ID_8905619,Human_RBP_ID_9401505,Human_RBP_ID_22105555,Human_RBP_ID_22534048,Human_RBP_ID_27827244 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 58679 RMVar_ID_58679 Human_SNP_ID_265293889 m1A Human chr6 + 4776748 4776748 4776748 GTGTCGGCCGCCCGGCGCCGGCGCCCGCCCCGACCCTGCCCCTCCCGCCCGCAACTCCGCCGCCC GTGTCGGCCGCCCGGCGCCGGCGCCCGCCCCGCCCCTGCCCCTCCCGCCCGCAACTCCGCCGCCC A C CDYL Ensembl:ENSG00000153046 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:4776378..4776825;chr6:4776372..4776747;chr6:4776334..4776842;chr6:4776567..4776750 26863196 MeRIP-seq:(Medium) rs1253146958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22534122 Human_Splice_Rec_734989,Human_Splice_Rec_735001 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 58680 RMVar_ID_58680 Human_SNP_ID_265298665 m1A Human chr6 + 4794148 4794148 4794148 AGGAGGTAAGCATAAGTAGAGAAGAGATGTGAAGACTGAATCCTGGGGGCACTGTAGCCGTCATC AGGAGGTAAGCATAAGTAGAGAAGAGATGTGAGGACTGAATCCTGGGGGCACTGTAGCCGTCATC A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:4794134..4794607 26863196 MeRIP-seq:(Medium) rs764247164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15841616 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 58681 RMVar_ID_58681 Human_SNP_ID_265324345 m1A Human chr6 + 4892258 4892258 4892258 GAAGTGGCAGCGGAAAAGCCGGTCGGAGCTTTATTGGGCCCCGGTGCCGAGAGGGCCAGGATGGG GAAGTGGCAGCGGAAAAGCCGGTCGGAGCTTTGTTGGGCCCCGGTGCCGAGAGGGCCAGGATGGG A G CDYL Ensembl:ENSG00000153046 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:4892120..4935571 32194978 MeRIP-seq:(Medium) rs140679987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665913,Human_RBP_ID_948508,Human_RBP_ID_3968542,Human_RBP_ID_4914679,Human_RBP_ID_9308513,Human_RBP_ID_9399862,Human_RBP_ID_18078049,Human_RBP_ID_22104553,Human_RBP_ID_22313606,Human_RBP_ID_22534123,Human_RBP_ID_26353347,Human_RBP_ID_27099251,Human_RBP_ID_27827249 Human_miRNA_ID_3104901,Human_miRNA_ID_3104902,Human_miRNA_ID_3104903,Human_miRNA_ID_3104904 RMVar_hsa_circ_127308,RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983,RMVar_hsa_circ_117762,RMVar_hsa_circ_107359,RMVar_hsa_circ_236984,RMVar_hsa_circ_345794,RMVar_hsa_circ_236985,RMVar_hsa_circ_278914,RMVar_hsa_circ_236987,RMVar_hsa_circ_236989,RMVar_hsa_circ_24166,RMVar_hsa_circ_236988,RMVar_hsa_circ_236986 58682 RMVar_ID_58682 Human_SNP_ID_265419167 m1A Human chr6 + 5260706 5260706 5260706 GCTCTCTCTCAGCATCGCCCGGTACAGAGATAACACTTGTGCGCGACTGGAGGCTGCCATTTTGG GCTCTCTCTCAGCATCGCCCGGTACAGAGATAGCACTTGTGCGCGACTGGAGGCTGCCATTTTGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:5260594..5260862 26863196 MeRIP-seq:(Medium) rs1390810768 Functional Loss SNV dbSNP153 33..33 33 - - - 58683 RMVar_ID_58683 Human_SNP_ID_265431457 m1A Human chr6 - 5309318 5309318 5309318 AGTGTCTCTCTCCCCTCTGTAAAGAGTACCCCATCCCTGCCTCTTAACCTTGAGTCCTCCTTCTC AGTGTCTCTCTCCCCTCTGTAAAGAGTACCCCGTCCCTGCCTCTTAACCTTGAGTCCTCCTTCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:5309236..5309365 26863196 MeRIP-seq:(Medium) rs903783085 Functional Loss SNV dbSNP153 33..33 33 - - - 58684 RMVar_ID_58684 Human_SNP_ID_265432497 m1A Human chr6 + 5314239 5314239 5314239 CCTGAAGGTTAAGGTGGGCTGATGGAGGAGGGAGTGGCAGTAGAGTTGGAAAGAGGCAGATGGAT CCTGAAGGTTAAGGTGGGCTGATGGAGGAGGGTGTGGCAGTAGAGTTGGAAAGAGGCAGATGGAT A T FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5314235..5314336 26863196 MeRIP-seq:(Medium) rs1230110261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997 58685 RMVar_ID_58685 Human_SNP_ID_265445680 m1A Human chr6 + 5368701 5368701 5368701 ATCGAGGCCTCCTGCAGCAGAGTGTGCCACCCAAAGAGCTCCAGGCAGTGTGGTGGAGCTGCTGG ATCGAGGCCTCCTGCAGCAGAGTGTGCCACCCGAAGAGCTCCAGGCAGTGTGGTGGAGCTGCTGG A G FARS2 Ensembl:ENSG00000145982 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:5368651..5404550 32194978 MeRIP-seq:(Medium) rs1453046888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_237001,RMVar_hsa_circ_286335,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997,RMVar_hsa_circ_303679,RMVar_hsa_circ_337412,RMVar_hsa_circ_301841,RMVar_hsa_circ_237003,RMVar_hsa_circ_278872,RMVar_hsa_circ_237002,RMVar_hsa_circ_236999,RMVar_hsa_circ_237000,RMVar_hsa_circ_236998 58686 RMVar_ID_58686 Human_SNP_ID_265466036 m1A Human chr6 - 5450276 5450276 5450276 GCCTTTCTGAAAGCTTCCCCAAGTCACACTAGATGCCACCTCCTACTCTTCCCACAGTGCAATGT GCCTTTCTGAAAGCTTCCCCAAGTCACACTAGGTGCCACCTCCTACTCTTCCCACAGTGCAATGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5450266..5450381 26863196 MeRIP-seq:(Medium) rs368133127 Functional Loss SNV dbSNP153 33..33 33 - - - 58687 RMVar_ID_58687 Human_SNP_ID_265466074 m1A Human chr6 - 5450418 5450418 5450418 GACCAAGGCCGCCCCAAACCCAAATGCCTACCACTTGGCCCCTTACCAAACTAGTTTGCCCCTGC GACCAAGGCCGCCCCAAACCCAAATGCCTACCGCTTGGCCCCTTACCAAACTAGTTTGCCCCTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:5450385..5450494 26863196 MeRIP-seq:(Medium) rs913473477 Functional Loss SNV dbSNP153 33..33 33 - - - 58688 RMVar_ID_58688 Human_SNP_ID_265488912 m1A Human chr6 - 5545245 5545245 5545245 ACACCAGAAGAGACGGATATCAGGGATGTCGTAGAGGATCATGGCTAGCCTTTCTAATCCTAGGC ACACCAGAAGAGACGGATATCAGGGATGTCGTGGAGGATCATGGCTAGCCTTTCTAATCCTAGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:5545194..5613316 32194978 MeRIP-seq:(Medium) rs1561701691 Functional Loss SNV dbSNP153 33..33 33 - - - 58689 RMVar_ID_58689 Human_SNP_ID_265494966 m1A Human chr6 - 5569766 5569766 5569766 CAACTACCTCTCCCCCATAACAATATGCCCTGACTTCACCTCCCCTGGACCATCCTCTCTTAAAG CAACTACCTCTCCCCCATAACAATATGCCCTGCCTTCACCTCCCCTGGACCATCCTCTCTTAAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5569736..5569858 26863196 MeRIP-seq:(Medium) rs1314395263 Functional Loss SNV dbSNP153 33..33 33 - - - 58690 RMVar_ID_58690 Human_SNP_ID_265494973 m1A Human chr6 + 5569790 5569790 5569790 AGGTGAAGTCAGGGCATATTGTTATGGGGGAGAGGTAGTTGCTGAGCAAGCACTGGCATGGGTTG AGGTGAAGTCAGGGCATATTGTTATGGGGGAGCGGTAGTTGCTGAGCAAGCACTGGCATGGGTTG A C FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:5569690..5569923 26863196 MeRIP-seq:(Medium) rs910535630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337412,RMVar_hsa_circ_114769,RMVar_hsa_circ_237006 58691 RMVar_ID_58691 Human_SNP_ID_265521982 m1A Human chr6 + 5682909 5682909 5682909 CATTTTAAGGAGAGTCAGGGAAGACTCCTGAGAAAGCAGGGAAGTAAGGGACCATGGAAAGGCTG CATTTTAAGGAGAGTCAGGGAAGACTCCTGAGGAAGCAGGGAAGTAAGGGACCATGGAAAGGCTG A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5682902..5683051 26863196 MeRIP-seq:(Medium) rs1561797069 Functional Loss SNV dbSNP153 33..33 33 - - - 58692 RMVar_ID_58692 Human_SNP_ID_265538414 m1A Human chr6 - 5750481 5750481 5750481 CTGACTGGGCCTCCTCTCTGGTCGTCTTGTTTATCTCTTGCCTGTCCTTCTCAACCAAGCTTCCT CTGACTGGGCCTCCTCTCTGGTCGTCTTGTTTTTCTCTTGCCTGTCCTTCTCAACCAAGCTTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5750476..5750738 26863196 MeRIP-seq:(Medium) rs1049738331 Functional Loss SNV dbSNP153 33..33 33 - - - 58693 RMVar_ID_58693 Human_SNP_ID_265538415 m1A Human chr6 - 5750481 5750481 5750481 CTGACTGGGCCTCCTCTCTGGTCGTCTTGTTTATCTCTTGCCTGTCCTTCTCAACCAAGCTTCCT CTGACTGGGCCTCCTCTCTGGTCGTCTTGTTTGTCTCTTGCCTGTCCTTCTCAACCAAGCTTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:5750476..5750738 26863196 MeRIP-seq:(Medium) rs1049738331 Functional Loss SNV dbSNP153 33..33 33 - - - 58694 RMVar_ID_58694 Human_SNP_ID_265543226 m1A Human chr6 + 5771434 5771434 5771434 GCTGTTGGGTGTGGAGGGCAGGTTCTGATGTCACCACTTCACTCAGGCTGCAGCCCTCTTGGGGC GCTGTTGGGTGTGGAGGGCAGGTTCTGATGTCGCCACTTCACTCAGGCTGCAGCCCTCTTGGGGC A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:5771383..5771482 32194978 MeRIP-seq:(Medium) rs1224250250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18079273 RMVar_hsa_circ_237015 58695 RMVar_ID_58695 Human_SNP_ID_265776590 m1A Human chr6 - 6683246 6683243 6683247 AGAGGGAAAGAGAAAGAGAAGGGGGAGAAAGAAAGGGAGAGACAGAGGAAGGGAGAGATGGGGAA AGAGGGAAAGAGAAAGAGAAGGGGGAGAAAG____GGAGAGACAGAGGAAGGGAGAGATGGGGAA CCTTT C AL031123.2 Ensembl:ENSG00000261211 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:6683137..6683430 26863196 MeRIP-seq:(Medium) rs1189921088 Functional Loss DEL dbSNP153 32..35 33 - - - 58696 RMVar_ID_58696 Human_SNP_ID_265779215 m1A Human chr6 + 6694971 6694971 6694971 CCTGTCGATGGCCTGCCAGCCTGCCGTGGGCCACTATCAGTCTGCTCTTACACCGGTGTGTTCCT CCTGTCGATGGCCTGCCAGCCTGCCGTGGGCCCCTATCAGTCTGCTCTTACACCGGTGTGTTCCT A C lnc-LY86-2,lnc-LY86-4 RNACentral:URS00008B441F,RNACentral:URS0000D5E29F lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:6694824..6695001 26863196 MeRIP-seq:(Medium) rs1172369547 Functional Loss SNV dbSNP153 33..33 33 - - - 58697 RMVar_ID_58697 Human_SNP_ID_265779217 m1A Human chr6 - 6694979 6694979 6694979 ACGTCAAGAGGAACACACCGGTGTAAGAGCAGACTGATAGTGGCCCACGGCAGGCTGGCAGGCCA ACGTCAAGAGGAACACACCGGTGTAAGAGCAGCCTGATAGTGGCCCACGGCAGGCTGGCAGGCCA T G AL031123.1 Ensembl:ENSG00000226281 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:6694857..6694979 26863196 MeRIP-seq:(Medium) rs904167050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5304833 58698 RMVar_ID_58698 Human_SNP_ID_265779316 m1A Human chr6 + 6695344 6695344 6695344 GAGTCCTTTGGTGAGGGAAACACTGGACACACAGAGGGCGGGCTGGAAGGGCAGGTGCTGGGAAG GAGTCCTTTGGTGAGGGAAACACTGGACACACGGAGGGCGGGCTGGAAGGGCAGGTGCTGGGAAG A G lnc-LY86-2 RNACentral:URS00008B441F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:6695298..6695418 26863196 MeRIP-seq:(Medium) rs541328002 Functional Loss SNV dbSNP153 33..33 33 - - - 58699 RMVar_ID_58699 Human_SNP_ID_265897609 m1A Human chr6 - 7129193 7129193 7129193 AGCCCCTACTTGTGCTTTTCCTAGAAGTGCAGACCCACTCCTGCGAGCTTCTGTGAGCCTTGGCC AGCCCCTACTTGTGCTTTTCCTAGAAGTGCAGGCCCACTCCTGCGAGCTTCTGTGAGCCTTGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7129186..7129275 26863196 MeRIP-seq:(Medium) rs1396262652 Functional Loss SNV dbSNP153 33..33 33 - - - 58700 RMVar_ID_58700 Human_SNP_ID_265908691 m1A Human chr6 + 7171713 7171713 7171713 CCATGATGAAGTGTGATGGGTGTGATGGCAACATTAGAGGTGAGTGTGTCCTGGAATTTGGAACC CCATGATGAAGTGTGATGGGTGTGATGGCAACGTTAGAGGTGAGTGTGTCCTGGAATTTGGAACC A G RREB1 Ensembl:ENSG00000124782 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7171706..7171902 26863196 MeRIP-seq:(Medium) rs1194938736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73104,RMVar_hsa_circ_125201,RMVar_hsa_circ_237028,RMVar_hsa_circ_328645 58701 RMVar_ID_58701 Human_SNP_ID_265924213 m1A Human chr6 + 7230197 7230197 7230197 ACCTGCGCACGCACAGTGGGGAGCGGCCCTACATTTGCAAGATCTGCCACTACCCCTTCACTGTC ACCTGCGCACGCACAGTGGGGAGCGGCCCTACGTTTGCAAGATCTGCCACTACCCCTTCACTGTC A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7230146..7230276 26863196 MeRIP-seq:(Medium) rs573607507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_292687,Human_miRNA_ID_870238 RMVar_hsa_circ_32361,RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_89958,RMVar_hsa_circ_237030,RMVar_hsa_circ_237039,RMVar_hsa_circ_373821,RMVar_hsa_circ_335838,RMVar_hsa_circ_318970,RMVar_hsa_circ_328228 58702 RMVar_ID_58702 Human_SNP_ID_265929270 m1A Human chr6 + 7246550 7246550 7246550 GCTCCGCCAGGTCGCAGGGGATGCGCCTGTGGAGCAGGCCACGGCGGAAACGGCCTCGCCGGTGC GCTCCGCCAGGTCGCAGGGGATGCGCCTGTGGCGCAGGCCACGGCGGAAACGGCCTCGCCGGTGC A C RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:7246501..7246700;chr6:7246501..7246835;chr6:7246501..7246602 26863196,32194978 MeRIP-seq:(Medium) rs1185556898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_950780,Human_RBP_ID_1048434,Human_RBP_ID_8905074,Human_RBP_ID_9309494,Human_RBP_ID_9354627,Human_RBP_ID_9399874,Human_RBP_ID_22727828 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58703 RMVar_ID_58703 Human_SNP_ID_265929271 m1A Human chr6 + 7246550 7246550 7246550 GCTCCGCCAGGTCGCAGGGGATGCGCCTGTGGAGCAGGCCACGGCGGAAACGGCCTCGCCGGTGC GCTCCGCCAGGTCGCAGGGGATGCGCCTGTGGGGCAGGCCACGGCGGAAACGGCCTCGCCGGTGC A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:7246501..7246700;chr6:7246501..7246835;chr6:7246501..7246602 26863196,32194978 MeRIP-seq:(Medium) rs1185556898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_950780,Human_RBP_ID_1048434,Human_RBP_ID_8905074,Human_RBP_ID_9309494,Human_RBP_ID_9354627,Human_RBP_ID_9399874,Human_RBP_ID_22727828 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58704 RMVar_ID_58704 Human_SNP_ID_265929277 m1A Human chr6 + 7246558 7246558 7246558 AGGTCGCAGGGGATGCGCCTGTGGAGCAGGCCACGGCGGAAACGGCCTCGCCGGTGCACCGGGAA AGGTCGCAGGGGATGCGCCTGTGGAGCAGGCCGCGGCGGAAACGGCCTCGCCGGTGCACCGGGAA A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7246510..7246703 26863196 MeRIP-seq:(Medium) rs370441334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1048434,Human_RBP_ID_8905074,Human_RBP_ID_9309494,Human_RBP_ID_9354627,Human_RBP_ID_9399874,Human_RBP_ID_22460868,Human_RBP_ID_22727828 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58705 RMVar_ID_58705 Human_SNP_ID_265929321 m1A Human chr6 + 7246607 7246607 7246607 GCCGGTGCACCGGGAAGAGCACGGGCGTGGGGAGAGCCATGAGCCGGAGGAGGAGCATGGCACTG GCCGGTGCACCGGGAAGAGCACGGGCGTGGGGGGAGCCATGAGCCGGAGGAGGAGCATGGCACTG A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7246496..7246704 26863196 MeRIP-seq:(Medium) rs1216061218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7624778,Human_RBP_ID_8905075,Human_RBP_ID_9309495,Human_RBP_ID_9354627,Human_RBP_ID_22460868,Human_RBP_ID_22727828 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58706 RMVar_ID_58706 Human_SNP_ID_265929582 m1A Human chr6 - 7246978 7246978 7246978 TTCCGCCGGGGCCTCCCCGGCACCCGGGGCCGACTCCACCACCTCTGCCGGGGTCTCGGGGGGCT TTCCGCCGGGGCCTCCCCGGCACCCGGGGCCGCCTCCACCACCTCTGCCGGGGTCTCGGGGGGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7246937..7247131 26863196 MeRIP-seq:(Medium) rs1273517893 Functional Loss SNV dbSNP153 33..33 33 - - - 58707 RMVar_ID_58707 Human_SNP_ID_265929675 m1A Human chr6 + 7247078 7247078 7247078 GGAGAGCGCGGCCGAGAAAAGGTCCTCAGAGAAGAGCGACGATGACAAGAAACCAAAGACAGACT GGAGAGCGCGGCCGAGAAAAGGTCCTCAGAGAGGAGCGACGATGACAAGAAACCAAAGACAGACT A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:7246790..7247218;chr6:7246815..7247175 26863196 MeRIP-seq:(Medium) rs1395519596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13330,Human_RBP_ID_5618131,Human_RBP_ID_9399876,Human_RBP_ID_18472007,Human_RBP_ID_26354683 Human_miRNA_ID_3116772 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58708 RMVar_ID_58708 Human_SNP_ID_265929677 m1A Human chr6 + 7247080 7247080 7247080 AGAGCGCGGCCGAGAAAAGGTCCTCAGAGAAGAGCGACGATGACAAGAAACCAAAGACAGACTCC AGAGCGCGGCCGAGAAAAGGTCCTCAGAGAAGGGCGACGATGACAAGAAACCAAAGACAGACTCC A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:7246887..7247172 26863196 MeRIP-seq:(Medium) rs1329219818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13330,Human_RBP_ID_5618131,Human_RBP_ID_9399876,Human_RBP_ID_18472007,Human_RBP_ID_26354683 Human_miRNA_ID_3116772 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58709 RMVar_ID_58709 Human_SNP_ID_265929688 m1A Human chr6 + 7247101 7247101 7247101 CCTCAGAGAAGAGCGACGATGACAAGAAACCAAAGACAGACTCCCCCAAAAGCGTGGCCAGCAAG CCTCAGAGAAGAGCGACGATGACAAGAAACCAGAGACAGACTCCCCCAAAAGCGTGGCCAGCAAG A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7247051..7247150 26863196 MeRIP-seq:(Medium) rs549841770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13330,Human_RBP_ID_9309090,Human_RBP_ID_9399876,Human_RBP_ID_18472007,Human_RBP_ID_19016404,Human_RBP_ID_26353082,Human_RBP_ID_27827257 Human_miRNA_ID_835722,Human_miRNA_ID_1348762,Human_miRNA_ID_1812408,Human_miRNA_ID_2359364,Human_miRNA_ID_3106739 RMVar_hsa_circ_237029,RMVar_hsa_circ_126517,RMVar_hsa_circ_47983 58710 RMVar_ID_58710 Human_SNP_ID_265930190 m1A Human chr6 + 7248604 7248604 7248604 TCGCCACCAGCGGATCCACCAGAAAGCCAGGCATGCCAAACACCACGGGAAGGACAGCGACAAGG TCGCCACCAGCGGATCCACCAGAAAGCCAGGCGTGCCAAACACCACGGGAAGGACAGCGACAAGG A G RREB1 Ensembl:ENSG00000124782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7248554..7248758 26863196 MeRIP-seq:(Medium) rs774151170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532298,Human_RBP_ID_8237300,Human_RBP_ID_26353361 Human_Splice_Rec_735538,Human_Splice_Rec_735584,Human_Splice_Rec_735612,Human_Splice_Rec_735634,Human_Splice_Rec_735670 58711 RMVar_ID_58711 Human_SNP_ID_265946950 m1A Human chr6 + 7309977 7309977 7309977 TCGGCTTCATCATCTTCATCCTCAATTATGGAATCTTCTACTGTTTCTTCATCCTCTGTAAGATC TCGGCTTCATCATCTTCATCCTCAATTATGGAGTCTTCTACTGTTTCTTCATCCTCTGTAAGATC A G RF00017-4503,RF00017-4498 RNACentral:URS00009569F7,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7309926..7310094 26863196 MeRIP-seq:(Medium) rs1031055448 Functional Loss SNV dbSNP153 33..33 33 - - - 58712 RMVar_ID_58712 Human_SNP_ID_265947889 m1A Human chr6 + 7313102 7313102 7313102 GGCAGGGAACACGAGTAAGAGAAGCAGCAGCAAGCGGGGGAGGAGTCTCATGGCGCTGCCGGTCC GGCAGGGAACACGAGTAAGAGAAGCAGCAGCAGGCGGGGGAGGAGTCTCATGGCGCTGCCGGTCC A G RF00017-4503,RF00017-4498 RNACentral:URS00009569F7,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr6:7313019..7313200;chr6:7313026..7313150 26863196,32194978 MeRIP-seq:(Medium) rs1414890179 Functional Loss SNV dbSNP153 33..33 33 - - - 58713 RMVar_ID_58713 Human_SNP_ID_265947931 m1A Human chr6 + 7313156 7313149 7313156 GCTGCCGGTCCAGTGTCCAGTTTCCGTCGGCTAAGGCTCTCGGCGGCTCCGGCGGTAATGGCGTT GCTGCCGGTCCAGTGTCCAGTTTCCG_______AGGCTCTCGGCGGCTCCGGCGGTAATGGCGTT GTCGGCTA G RF00017-4503,RF00017-4498 RNACentral:URS00009569F7,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:7313066..7313175 26863410 MeRIP-seq:(Medium) rs753193831 Functional Loss DEL dbSNP153 27..33 33 - - - 58714 RMVar_ID_58714 Human_SNP_ID_265955864 m1A Human chr6 - 7339454 7339454 7339454 AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGATGCGAGTTACACCAACCAGGACAGAAATCATT AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGGTGCGAGTTACACCAACCAGGACAGAAATCATT T C AL139095.2,SSR1,CAGE1 Ensembl:ENSG00000220472,Ensembl:ENSG00000124783,Ensembl:ENSG00000164304 Pseudogene,Protein coding,Protein coding exon,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs780641426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17711605 58715 RMVar_ID_58715 Human_SNP_ID_265970029 m1A Human chr6 + 7393200 7393198 7393201 GAATGAGAATGGTGAAGGTGAAATAGAAGATGAGGAGGAGGAGGGTTATGACGATGATGATGATG GAATGAGAATGGTGAAGGTGAAATAGAAGAT___GAGGAGGAGGGTTATGACGATGATGATGATG TGAG T RIOK1 Ensembl:ENSG00000124784 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7393151..7393275 26863196 MeRIP-seq:(Medium) rs759262612 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3969510,Human_RBP_ID_4915479,Human_RBP_ID_7626509,Human_RBP_ID_9444291,Human_RBP_ID_24170943 RMVar_hsa_circ_112397,RMVar_hsa_circ_122053,RMVar_hsa_circ_115987,RMVar_hsa_circ_63429,RMVar_hsa_circ_237057,RMVar_hsa_circ_237058,RMVar_hsa_circ_237056 58716 RMVar_ID_58716 Human_SNP_ID_265975340 m1A Human chr6 + 7414377 7414377 7414377 TGCCCGCCCCAAGAAACACACCACGGACCCTGACATTGATAAAAAAGTAAGCAATGAAATACCTT TGCCCGCCCCAAGAAACACACCACGGACCCTGGCATTGATAAAAAAGTAAGCAATGAAATACCTT A G RIOK1 Ensembl:ENSG00000124784 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:7414326..7417450 26863196 MeRIP-seq:(Medium) rs775270644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22682369,Human_RBP_ID_24171023 Human_Splice_Rec_736021,Human_Splice_Rec_736045 RMVar_hsa_circ_277822,RMVar_hsa_circ_359371,RMVar_hsa_circ_237064,RMVar_hsa_circ_124339,RMVar_hsa_circ_237065 58717 RMVar_ID_58717 Human_SNP_ID_265976103 m1A Human chr6 + 7417402 7417402 7417402 AGAAAAAACAAAATTCCTAAACATGTGAAAAAAAGAAAGGAGAAGACAGCCAAGACGAAAAAAGG AGAAAAAACAAAATTCCTAAACATGTGAAAAAGAGAAAGGAGAAGACAGCCAAGACGAAAAAAGG A G RIOK1 Ensembl:ENSG00000124784 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7417300..7417421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_80097,Human_RBP_ID_3017201,Human_RBP_ID_23064720 Human_Splice_Rec_736022,Human_Splice_Rec_736046 RMVar_hsa_circ_124339,RMVar_hsa_circ_237065 58718 RMVar_ID_58718 Human_SNP_ID_266011231 m1A Human chr6 - 7541691 7541691 7541691 GGGGCAGGAGCGGGAGGAAAGCTGTGGCTCGGAGGGCGGCAAGGGCGCAGAGGAGCTGCGTCGGA GGGGCAGGAGCGGGAGGAAAGCTGTGGCTCGGGGGGCGGCAAGGGCGCAGAGGAGCTGCGTCGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7541576..7542028 26863196 MeRIP-seq:(Medium) rs138647938 Functional Loss SNV dbSNP153 33..33 33 - - - 58719 RMVar_ID_58719 Human_SNP_ID_266011256 m1A Human chr6 + 7541784 7541754 7541784 CGGCCTCGGGAGGGCCCAGGTAGCGAGCAGCGACCTCGCGAGCCTTCCGCACTCCCGCCCGGTTC CGG______________________________CCTCGCGAGCCTTCCGCACTCCCGCCCGGTTC GCCTCGGGAGGGCCCAGGTAGCGAGCAGCGA G DSP Ensembl:ENSG00000096696 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:7541601..7541950 26863196 MeRIP-seq:(Medium) rs1310361806 Functional Loss DEL dbSNP153 4..33 33 - - - Human_RBP_ID_842302,Human_RBP_ID_4903087,Human_RBP_ID_22460873 RMVar_hsa_circ_98792,RMVar_hsa_circ_237066 58720 RMVar_ID_58720 Human_SNP_ID_266011268 m1A Human chr6 - 7541796 7541794 7541797 CGGACGGCCGGGGAACCGGGCGGGAGTGCGGAAGGCTCGCGAGGTCGCTGCTCGCTACCTGGGCC CGGACGGCCGGGGAACCGGGCGGGAGTGCGG___GCTCGCGAGGTCGCTGCTCGCTACCTGGGCC CCTT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7541551..7541927 26863196 MeRIP-seq:(Medium) rs1336339919 Functional Loss DEL dbSNP153 32..34 33 - - - 58721 RMVar_ID_58721 Human_SNP_ID_266011363 m1A Human chr6 - 7541968 7541968 7541968 CGTAGCGCAGGTCCGGGCCAGACTCGGCGCGGATCATGCGGCCCAGAGTGTTGATCCGCGGGTGG CGTAGCGCAGGTCCGGGCCAGACTCGGCGCGGGTCATGCGGCCCAGAGTGTTGATCCGCGGGTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7541951..7541975 26863196 MeRIP-seq:(Medium) rs769533657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_668001 58722 RMVar_ID_58722 Human_SNP_ID_266016910 m1A Human chr6 + 7562658 7562658 7562658 CGCCTCTCTTTGTCTTTGTGTCGCAGGCGGAGATGGACATGGTGGCCTGGGGTGTGGACCTGGCC CGCCTCTCTTTGTCTTTGTGTCGCAGGCGGAGGTGGACATGGTGGCCTGGGGTGTGGACCTGGCC A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:7562651..7562700 26863196 MeRIP-seq:(Medium) rs1184593852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79271,Human_RBP_ID_789731,Human_RBP_ID_948033,Human_RBP_ID_5532302,Human_RBP_ID_8903248,Human_RBP_ID_9401536,Human_RBP_ID_18086080,Human_RBP_ID_18472194,Human_RBP_ID_19017764,Human_RBP_ID_22460880,Human_RBP_ID_26037987 Human_Splice_Rec_736060,Human_Splice_Rec_736106,Human_Splice_Rec_736146 RMVar_hsa_circ_65575,RMVar_hsa_circ_98792,RMVar_hsa_circ_356334,RMVar_hsa_circ_237066,RMVar_hsa_circ_74547,RMVar_hsa_circ_237067 58723 RMVar_ID_58723 Human_SNP_ID_266021524 m1A Human chr6 + 7579748 7579748 7579748 GTTCTACTGCAGGAAGAAGGCACCCGGAAGAGAGAATATGAAAATGAGCTGGCAAAGGTAAGAAA GTTCTACTGCAGGAAGAAGGCACCCGGAAGAGGGAATATGAAAATGAGCTGGCAAAGGTAAGAAA A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7579499..7579836 26863196 MeRIP-seq:(Medium) rs754299901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3017580,Human_RBP_ID_7627561,Human_RBP_ID_8903334,Human_RBP_ID_9399929,Human_RBP_ID_27525948 Human_Splice_Rec_736097 58724 RMVar_ID_58724 Human_SNP_ID_266022070 m1A Human chr6 - 7581046 7581046 7581046 CACTCCTCTTCTTAACAATGGATGCCTGCTCCAGCTGCTGGGTCAGGTTGGTGATTTTGATGGCT CACTCCTCTTCTTAACAATGGATGCCTGCTCCCGCTGCTGGGTCAGGTTGGTGATTTTGATGGCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7581026..7581050 26863196 MeRIP-seq:(Medium) rs1348541237 Functional Loss SNV dbSNP153 33..33 33 - - - 58725 RMVar_ID_58725 Human_SNP_ID_266022103 m1A Human chr6 + 7581112 7581112 7581112 GGATGACCTCCGGCAGCAGAGGGACGTGCTGGATGGCCACCTGAGGGAAAAGCAGAGGACCCAGG GGATGACCTCCGGCAGCAGAGGGACGTGCTGGGTGGCCACCTGAGGGAAAAGCAGAGGACCCAGG A G DSP Ensembl:ENSG00000096696 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:7581067..7581225 26863196 MeRIP-seq:(Medium) rs765847051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81322,Human_RBP_ID_215441,Human_RBP_ID_668007,Human_RBP_ID_791936,Human_RBP_ID_948034,Human_RBP_ID_5217209,Human_RBP_ID_5478518,Human_RBP_ID_8237319,Human_RBP_ID_9399935,Human_RBP_ID_18472197,Human_RBP_ID_18869134,Human_RBP_ID_19016411,Human_RBP_ID_21389477,Human_RBP_ID_26353095 58726 RMVar_ID_58726 Human_SNP_ID_266022104 m1A Human chr6 + 7581112 7581112 7581112 GGATGACCTCCGGCAGCAGAGGGACGTGCTGGATGGCCACCTGAGGGAAAAGCAGAGGACCCAGG GGATGACCTCCGGCAGCAGAGGGACGTGCTGGTTGGCCACCTGAGGGAAAAGCAGAGGACCCAGG A T DSP Ensembl:ENSG00000096696 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:7581067..7581225 26863196 MeRIP-seq:(Medium) rs765847051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81322,Human_RBP_ID_215441,Human_RBP_ID_668007,Human_RBP_ID_791936,Human_RBP_ID_948034,Human_RBP_ID_5217209,Human_RBP_ID_5478518,Human_RBP_ID_8237319,Human_RBP_ID_9399935,Human_RBP_ID_18472197,Human_RBP_ID_18869134,Human_RBP_ID_19016411,Human_RBP_ID_21389477,Human_RBP_ID_26353095 58727 RMVar_ID_58727 Human_SNP_ID_266022570 m1A Human chr6 + 7582771 7582771 7582771 AGGCAAGGCTGCAGAGGCTGGAGGATGAGCTGAATCGTGCAAAATCAACTCTAGAGGCAGAAACC AGGCAAGGCTGCAGAGGCTGGAGGATGAGCTGGATCGTGCAAAATCAACTCTAGAGGCAGAAACC A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:7582626..7582975 26863196 MeRIP-seq:(Medium) rs1297636815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3017658,Human_RBP_ID_5618165,Human_RBP_ID_8903371,Human_RBP_ID_17711258,Human_RBP_ID_23120260,Human_RBP_ID_24171343 58728 RMVar_ID_58728 Human_SNP_ID_266022620 m1A Human chr6 + 7582913 7582913 7582913 CAAGGAGGAGGCTATTAGGAAGATAGAATCGGAAAGAGAAAAGAGTGAGAGAGAGAAGAACAGTC CAAGGAGGAGGCTATTAGGAAGATAGAATCGGGAAGAGAAAAGAGTGAGAGAGAGAAGAACAGTC A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:7582676..7583199;chr6:7582693..7583075;chr6:7582719..7583121;chr6:7582703..7583050 26863196 MeRIP-seq:(Medium) rs1414563217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4897336,Human_RBP_ID_8903374 58729 RMVar_ID_58729 Human_SNP_ID_266022642 m1A Human chr6 + 7582951 7582951 7582951 AAAAGAGTGAGAGAGAGAAGAACAGTCTTAGGAGTGAGATCGAAAGACTCCAAGCAGAGATCAAG AAAAGAGTGAGAGAGAGAAGAACAGTCTTAGGGGTGAGATCGAAAGACTCCAAGCAGAGATCAAG A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7582926..7582950 26863196 MeRIP-seq:(Medium) rs1420813331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5618167,Human_RBP_ID_8903375 58730 RMVar_ID_58730 Human_SNP_ID_266023349 m1A Human chr6 + 7584970 7584970 7584970 ACATGATCTCCTTGAAAAATGGTGTCGGCACCAGCAGCAGCATGGGCAGTGGTGTCAGCGATGAT ACATGATCTCCTTGAAAAATGGTGTCGGCACCGGCAGCAGCATGGGCAGTGGTGTCAGCGATGAT A G DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7584919..7585054 26863196 MeRIP-seq:(Medium) rs1456123705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7627598,Human_RBP_ID_8903437,Human_RBP_ID_15876218 58731 RMVar_ID_58731 Human_SNP_ID_266023518 m1A Human chr6 + 7585379 7585379 7585379 CATAGGCTTCGAGGGTGTGAAGGGAAAGAAGAAGATGTCAGCAGCAGAGGCAGTGAAAGAAAAAT CATAGGCTTCGAGGGTGTGAAGGGAAAGAAGATGATGTCAGCAGCAGAGGCAGTGAAAGAAAAAT A T DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7585328..7585540 26863196 MeRIP-seq:(Medium) rs537588390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81338,Human_RBP_ID_1048597,Human_RBP_ID_2026108 Clinvar_Rec_192 58732 RMVar_ID_58732 Human_SNP_ID_266024882 m1A Human chr6 - 7590278 7590258 7590279 AGCTCCTCCTGCAGCCGCCGCCGCTCCTCCACAGGTGGAGGCTCGCCCTCCATAGCTGCAGCCCA AGCTCCTCCTGCAGCCGCCGCCGCTCCTCCA_____________________TAGCTGCAGCCCA ATGGAGGGCGAGCCTCCACCTG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7590201..7593768 26863196 MeRIP-seq:(Medium) rs1338729581 Functional Loss DEL dbSNP153 32..52 33 - - - 58733 RMVar_ID_58733 Human_SNP_ID_266024905 m1A Human chr6 + 7590283 7590283 7590283 TGCAGCTATGGAGGGCGAGCCTCCACCTGTGGAGGAGCGGCGGCGGCTGCAGGAGGAGCTGAACG TGCAGCTATGGAGGGCGAGCCTCCACCTGTGGCGGAGCGGCGGCGGCTGCAGGAGGAGCTGAACG A C SNRNP48 Ensembl:ENSG00000168566 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:7590232..7590358 26863196 MeRIP-seq:(Medium) rs145014878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252362,Human_RBP_ID_668044,Human_RBP_ID_791101,Human_RBP_ID_948035,Human_RBP_ID_4903090,Human_RBP_ID_9309093,Human_RBP_ID_18425561,Human_RBP_ID_23067766,Human_RBP_ID_27827270 58734 RMVar_ID_58734 Human_SNP_ID_266025421 m1A Human chr6 - 7592195 7592195 7592195 TTCTACACATGCTGTTGATGCTTCTTCCCCGCACCCGCCAACCCCCTAGCCAATTCAACTCACTT TTCTACACATGCTGTTGATGCTTCTTCCCCGCCCCCGCCAACCCCCTAGCCAATTCAACTCACTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7592192..7592318 26863196 MeRIP-seq:(Medium) rs988129869 Functional Loss SNV dbSNP153 33..33 33 - - - 58735 RMVar_ID_58735 Human_SNP_ID_266028743 m1A Human chr6 + 7606150 7606147 7606151 TAGGAGTAGAAGCCCACATAAAAGAAAAAGAAACAAAGATAAGGATAAAAACTGTGAGTCGAGAA TAGGAGTAGAAGCCCACATAAAAGAAAAAG____AAAGATAAGGATAAAAACTGTGAGTCGAGAA GAAAC G SNRNP48 Ensembl:ENSG00000168566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7606026..7608825 26863196 MeRIP-seq:(Medium) rs765335450 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_668234,Human_RBP_ID_5622355,Human_RBP_ID_7628196,Human_RBP_ID_24171612,Human_RBP_ID_24548664 Human_Splice_Rec_736165,Human_Splice_Rec_736187 RMVar_hsa_circ_19055,RMVar_hsa_circ_109071,RMVar_hsa_circ_296659,RMVar_hsa_circ_75458,RMVar_hsa_circ_237073,RMVar_hsa_circ_365189,RMVar_hsa_circ_237074 58736 RMVar_ID_58736 Human_SNP_ID_266028744 m1A Human chr6 + 7606150 7606150 7606150 TAGGAGTAGAAGCCCACATAAAAGAAAAAGAAACAAAGATAAGGATAAAAACTGTGAGTCGAGAA TAGGAGTAGAAGCCCACATAAAAGAAAAAGAAGCAAAGATAAGGATAAAAACTGTGAGTCGAGAA A G SNRNP48 Ensembl:ENSG00000168566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7606026..7608825 26863196 MeRIP-seq:(Medium) rs1392832714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_668234,Human_RBP_ID_5622355,Human_RBP_ID_7628196,Human_RBP_ID_24171612,Human_RBP_ID_24548664 Human_Splice_Rec_736165,Human_Splice_Rec_736187 RMVar_hsa_circ_19055,RMVar_hsa_circ_109071,RMVar_hsa_circ_296659,RMVar_hsa_circ_75458,RMVar_hsa_circ_237073,RMVar_hsa_circ_365189,RMVar_hsa_circ_237074 58737 RMVar_ID_58737 Human_SNP_ID_266028745 m1A Human chr6 + 7606152 7606152 7606152 GGAGTAGAAGCCCACATAAAAGAAAAAGAAACAAAGATAAGGATAAAAACTGTGAGTCGAGAAGA GGAGTAGAAGCCCACATAAAAGAAAAAGAAACGAAGATAAGGATAAAAACTGTGAGTCGAGAAGA A G SNRNP48 Ensembl:ENSG00000168566 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7606026..7608825 26863196 MeRIP-seq:(Medium) rs1307196231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_668234,Human_RBP_ID_5622355,Human_RBP_ID_7628196,Human_RBP_ID_24171612,Human_RBP_ID_24548664 Human_Splice_Rec_736165,Human_Splice_Rec_736187 RMVar_hsa_circ_19055,RMVar_hsa_circ_109071,RMVar_hsa_circ_296659,RMVar_hsa_circ_75458,RMVar_hsa_circ_237073,RMVar_hsa_circ_365189,RMVar_hsa_circ_237074 58738 RMVar_ID_58738 Human_SNP_ID_266056448 m1A Human chr6 - 7726310 7726310 7726310 CCTGAGCTCTCGGGCACCGTCGCTCCCACTCAAAATCTCCGCGCGCCGCACGCCTCCTCAAGCGG CCTGAGCTCTCGGGCACCGTCGCTCCCACTCAGAATCTCCGCGCGCCGCACGCCTCCTCAAGCGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:7726189..7726374 26863196 MeRIP-seq:(Medium) rs145653316 Functional Loss SNV dbSNP153 33..33 33 - - - 58739 RMVar_ID_58739 Human_SNP_ID_266056817 m1A Human chr6 - 7727215 7727215 7727215 CGTGCAGGGGCCGGGGCCGGTGCGGGAGCCCCAGCACCGACAAGATCTCCTTCTGCATCTCCCGC CGTGCAGGGGCCGGGGCCGGTGCGGGAGCCCCGGCACCGACAAGATCTCCTTCTGCATCTCCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7727167..7727317 26863196 MeRIP-seq:(Medium) rs1561750275 Functional Loss SNV dbSNP153 33..33 33 - - - 58740 RMVar_ID_58740 Human_SNP_ID_266057008 m1A Human chr6 - 7727433 7727433 7727433 CTGGGACGAGCTGGCTGCTTCGTGGGGCCAGGACTGCTGCCTCTCCCCCTCCGACGCCCCGTCCT CTGGGACGAGCTGGCTGCTTCGTGGGGCCAGGTCTGCTGCCTCTCCCCCTCCGACGCCCCGTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7727384..7727569 26863196 MeRIP-seq:(Medium) rs771981511 Functional Loss SNV dbSNP153 33..33 33 - - - 58741 RMVar_ID_58741 Human_SNP_ID_266057009 m1A Human chr6 - 7727433 7727433 7727433 CTGGGACGAGCTGGCTGCTTCGTGGGGCCAGGACTGCTGCCTCTCCCCCTCCGACGCCCCGTCCT CTGGGACGAGCTGGCTGCTTCGTGGGGCCAGGGCTGCTGCCTCTCCCCCTCCGACGCCCCGTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7727384..7727569 26863196 MeRIP-seq:(Medium) rs771981511 Functional Loss SNV dbSNP153 33..33 33 - - - 58742 RMVar_ID_58742 Human_SNP_ID_266073914 m1A Human chr6 + 7795530 7795530 7795530 GGTCCTGGCTACAAAGGGCTAGTTTGTCATGAAGCCACTTAGATTCAACCCCACAGCTGATGACA GGTCCTGGCTACAAAGGGCTAGTTTGTCATGAGGCCACTTAGATTCAACCCCACAGCTGATGACA A G BMP6 Ensembl:ENSG00000153162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7795493..7795599 26863196 MeRIP-seq:(Medium) rs1219121853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106738,RMVar_hsa_circ_116306,RMVar_hsa_circ_237075,RMVar_hsa_circ_237076 58743 RMVar_ID_58743 Human_SNP_ID_266083721 m1A Human chr6 - 7833391 7833391 7833391 TCTGTCTCTAGCTCTGTCTACCCTGCCACCCTAAATTGCCCAATTAATCATCAACTCTTGTTGCT TCTGTCTCTAGCTCTGTCTACCCTGCCACCCTCAATTGCCCAATTAATCATCAACTCTTGTTGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:7833377..7833465 26863196 MeRIP-seq:(Medium) rs1309729852 Functional Loss SNV dbSNP153 33..33 33 - - - 58744 RMVar_ID_58744 Human_SNP_ID_266096556 m1A Human chr6 + 7882048 7882048 7882048 CAACAGCTGCCACAGCCGTGCACACCAGGGCCAGAGCAGCCCACTGACATCTGTCTTTGGTCTTG CAACAGCTGCCACAGCCGTGCACACCAGGGCCGGAGCAGCCCACTGACATCTGTCTTTGGTCTTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:7881776..7882400 32194978 MeRIP-seq:(Medium) rs577534909 Functional Loss SNV dbSNP153 33..33 33 - - - 58745 RMVar_ID_58745 Human_SNP_ID_266096889 m1A Human chr6 + 7883088 7883088 7883088 CACTGGGAACCCAGTGGCCTCTGTGGGACTGAACTCCTAAACGCAGGGTGCGGGAGCTGGGCAGG CACTGGGAACCCAGTGGCCTCTGTGGGACTGACCTCCTAAACGCAGGGTGCGGGAGCTGGGCAGG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:7882901..7883275 32194978 MeRIP-seq:(Medium) rs1371752491 Functional Loss SNV dbSNP153 33..33 33 - - - 58746 RMVar_ID_58746 Human_SNP_ID_266096938 m1A Human chr6 - 7883190 7883190 7883190 AGTCAGTGAGCACAGTGGAGGCAGAGACCTTGACTCGTTACACCGCTTTGTCCTGAGCCAAGCGA AGTCAGTGAGCACAGTGGAGGCAGAGACCTTGGCTCGTTACACCGCTTTGTCCTGAGCCAAGCGA T C BLOC1S5-TXNDC5,TXNDC5 Ensembl:ENSG00000259040,Ensembl:ENSG00000239264 Protein coding,Protein coding 3'UTR,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:7883139..7883274 26863196 MeRIP-seq:(Medium) rs202149821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_668540,Human_RBP_ID_791573,Human_RBP_ID_7630132,Human_RBP_ID_8649279,Human_RBP_ID_8903622,Human_RBP_ID_15881816,Human_RBP_ID_18084685,Human_RBP_ID_21222343,Human_RBP_ID_22773241,Human_RBP_ID_22832249,Human_RBP_ID_24513350,Human_RBP_ID_27526072 Human_Splice_Rec_736206,Human_Splice_Rec_736224,Human_Splice_Rec_736242,Human_Splice_Rec_736248,Human_Splice_Rec_736274 58747 RMVar_ID_58747 Human_SNP_ID_266096958 m1A Human chr6 + 7883220 7883220 7883220 AGTCAAGGTCTCTGCCTCCACTGTGCTCACTGACTTTCTTCCCTCCTCGGAAAAGCAATAACGTG AGTCAAGGTCTCTGCCTCCACTGTGCTCACTGCCTTTCTTCCCTCCTCGGAAAAGCAATAACGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7883087..7883300 26863196 MeRIP-seq:(Medium) rs776224289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27526073 58748 RMVar_ID_58748 Human_SNP_ID_266098263 m1A Human chr6 + 7887473 7887473 7887473 GCTGGGTACCATCCTCCACCAGATATGCGGGAATCAGACTCGCCTCGGACCCTCCCTCCCTCTCC GCTGGGTACCATCCTCCACCAGATATGCGGGACTCAGACTCGCCTCGGACCCTCCCTCCCTCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7887471..7888009 26863196 MeRIP-seq:(Medium) rs1007867705 Functional Loss SNV dbSNP153 33..33 33 - - - 58749 RMVar_ID_58749 Human_SNP_ID_266098958 m1A Human chr6 + 7889455 7889455 7889455 AAACCACTCAGTAGCTCAGCCTGATGGGGTTAAGAGATGAAGAATTCTCAGTACTAAGAAGTGCA AAACCACTCAGTAGCTCAGCCTGATGGGGTTAGGAGATGAAGAATTCTCAGTACTAAGAAGTGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7889453..7889619 26863196 MeRIP-seq:(Medium) rs770403407 Functional Loss SNV dbSNP153 33..33 33 - - - 58750 RMVar_ID_58750 Human_SNP_ID_266101627 m1A Human chr6 - 7899676 7899676 7899676 CTGTCTAATCCTTTGTTATTCTTTCAGCTTAAAGCTTTTCAAGCCAGGCCAAGAAGCTGTGAAGT CTGTCTAATCCTTTGTTATTCTTTCAGCTTAACGCTTTTCAAGCCAGGCCAAGAAGCTGTGAAGT T G BLOC1S5-TXNDC5,TXNDC5 Ensembl:ENSG00000259040,Ensembl:ENSG00000239264 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7899528..7899729 26863196 MeRIP-seq:(Medium) rs145133420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9350119 Human_Splice_Rec_736210,Human_Splice_Rec_736228,Human_Splice_Rec_736260 RMVar_hsa_circ_64775,RMVar_hsa_circ_63059,RMVar_hsa_circ_237088,RMVar_hsa_circ_80608,RMVar_hsa_circ_331363,RMVar_hsa_circ_237089,RMVar_hsa_circ_301163 58751 RMVar_ID_58751 Human_SNP_ID_266104593 m1A Human chr6 - 7910613 7910613 7910613 GGCGGCGGACGGGCCCCCCGCGGCAGACGGCGAGGACGGACAGGACCCGCACAGCAAGCACCTGT GGCGGCGGACGGGCCCCCCGCGGCAGACGGCGTGGACGGACAGGACCCGCACAGCAAGCACCTGT T A BLOC1S5-TXNDC5,TXNDC5 Ensembl:ENSG00000259040,Ensembl:ENSG00000239264 Protein coding,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:7910540..7910750 26863196 MeRIP-seq:(Medium) rs1359440935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170609,Human_RBP_ID_251831,Human_RBP_ID_842182,Human_RBP_ID_3968550,Human_RBP_ID_4898206,Human_RBP_ID_5327036,Human_RBP_ID_9309096,Human_RBP_ID_9336438,Human_RBP_ID_22460908 Human_Splice_Rec_736207 RMVar_hsa_circ_124740,RMVar_hsa_circ_80608,RMVar_hsa_circ_237089,RMVar_hsa_circ_237090 58752 RMVar_ID_58752 Human_SNP_ID_266104658 m1A Human chr6 + 7910700 7910698 7910701 GGGCGCCCCAGCGCCCGCCGCCGCCATGGCCCAGCAGCAGCAGCAGCAGCGCAGTCAGGGCCGCC GGGCGCCCCAGCGCCCGCCGCCGCCATGGCC___CAGCAGCAGCAGCAGCGCAGTCAGGGCCGCC CCAG C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:7910599..7910780 26863410 MeRIP-seq:(Medium) rs775841007 Functional Loss DEL dbSNP153 32..34 33 - - - 58753 RMVar_ID_58753 Human_SNP_ID_266151379 m1A Human chr6 - 8102495 8102495 8102495 CGGAAGATGGCGGCGGCCGCAGAGTTGTCGCTACTGGAGAAGTCCCTGGGACTGAGTAAGGGGAA CGGAAGATGGCGGCGGCCGCAGAGTTGTCGCTGCTGGAGAAGTCCCTGGGACTGAGTAAGGGGAA T C EEF1E1,EEF1E1-BLOC1S5 Ensembl:ENSG00000124802,Ensembl:ENSG00000265818 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:8097351..8102578 26863196 MeRIP-seq:(Medium) rs1364975454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81661,Human_RBP_ID_1676664,Human_RBP_ID_4898963,Human_RBP_ID_5512037,Human_RBP_ID_7634261,Human_RBP_ID_8649815,Human_RBP_ID_8903806,Human_RBP_ID_9198946,Human_RBP_ID_15888296,Human_RBP_ID_18425352,Human_RBP_ID_22460911,Human_RBP_ID_23067286 Human_Splice_Rec_736317,Human_Splice_Rec_736329,Human_Splice_Rec_736335,Human_Splice_Rec_736341,Human_Splice_Rec_736347 58754 RMVar_ID_58754 Human_SNP_ID_266232100 m1A Human chr6 - 8430156 8430156 8430156 AAATGTTTTAATTGCTTATTTCCTTCTCTAGGACTTGACACAGCAAGCAAAAGACATACAGAACA AAATGTTTTAATTGCTTATTTCCTTCTCTAGGGCTTGACACAGCAAGCAAAAGACATACAGAACA T C SLC35B3 Ensembl:ENSG00000124786 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:8430112..8435086 26863196 MeRIP-seq:(Medium) rs1333913627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22682381 Human_Splice_Rec_736462,Human_Splice_Rec_736484,Human_Splice_Rec_736504,Human_Splice_Rec_736524,Human_Splice_Rec_736546 RMVar_hsa_circ_333894,RMVar_hsa_circ_237092,RMVar_hsa_circ_372881,RMVar_hsa_circ_328237,RMVar_hsa_circ_350108,RMVar_hsa_circ_237093 58755 RMVar_ID_58755 Human_SNP_ID_266284204 m1A Human chr6 - 8644924 8644924 8644924 TCGTGGTGAGTGTTACAGCTCTTAAAAGTGGCACAGCCCCAAAAAGTAACCAACAGCAAAATTTA TCGTGGTGAGTGTTACAGCTCTTAAAAGTGGCGCAGCCCCAAAAAGTAACCAACAGCAAAATTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:8644889..8644981 26863196 MeRIP-seq:(Medium) rs1052044639 Functional Loss SNV dbSNP153 33..33 33 - - - 58756 RMVar_ID_58756 Human_SNP_ID_266723230 m1A Human chr6 - 10383399 10383399 10383399 AGTCGGCCTTTGTTCTGGCACTTTCAGGGCCTAGGAGTTAGGCAACTCTGGGGAGGTGCGAGGGG AGTCGGCCTTTGTTCTGGCACTTTCAGGGCCTGGGAGTTAGGCAACTCTGGGGAGGTGCGAGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:10383349..10383516 26863196 MeRIP-seq:(Medium) rs1232557305 Functional Loss SNV dbSNP153 33..33 33 - - - 58757 RMVar_ID_58757 Human_SNP_ID_266726851 m1A Human chr6 - 10398214 10398214 10398214 CCCTCTCGACTGTCAGTGGGGCAGCCTCTCCGACTCTGCACCCGCCTCGACCTCCCCACCCGCTC CCCTCTCGACTGTCAGTGGGGCAGCCTCTCCGTCTCTGCACCCGCCTCGACCTCCCCACCCGCTC T A TFAP2A Ensembl:ENSG00000137203 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:10398049..10398449 26863410 MeRIP-seq:(Medium) rs944946792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_649583,Human_RBP_ID_1043347,Human_RBP_ID_17303986 58758 RMVar_ID_58758 Human_SNP_ID_266726967 m1A Human chr6 + 10398394 10398394 10398394 GGTGGGCGCGCGGGGGGCTGGTGAGGCGTGGGAGGGGCGGGGCGGGAGGAGAGCCTCACTTTCTG GGTGGGCGCGCGGGGGGCTGGTGAGGCGTGGGGGGGGCGGGGCGGGAGGAGAGCCTCACTTTCTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:10398376..10398400 26863196 MeRIP-seq:(Medium) rs1021755301 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 58759 RMVar_ID_58759 Human_SNP_ID_266727008 m1A Human chr6 + 10398496 10398496 10398496 CCGTGTGGCTGTTGGGGTTGTTGCTGAGGTACATTTTGTCCATGGCCTTGAGGGCCTCGGTGAGA CCGTGTGGCTGTTGGGGTTGTTGCTGAGGTACCTTTTGTCCATGGCCTTGAGGGCCTCGGTGAGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:10398147..10398601 26863196 MeRIP-seq:(Medium) rs1332712198 Functional Loss SNV dbSNP153 33..33 33 - - - 58760 RMVar_ID_58760 Human_SNP_ID_266730206 m1A Human chr6 - 10409952 10409952 10409952 CTCCTGCACGGCCCACACGCGCTCAGCTCAGGACTCGGAGACCTCTCGATCCACTCCTTACCTCA CTCCTGCACGGCCCACACGCGCTCAGCTCAGGGCTCGGAGACCTCTCGATCCACTCCTTACCTCA T C TFAP2A Ensembl:ENSG00000137203 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10409871..10410364 26863196 MeRIP-seq:(Medium) rs777729482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8894842,Human_RBP_ID_15579757,Human_RBP_ID_17303995,Human_RBP_ID_27518457 Human_Splice_Rec_737847,Human_Splice_Rec_737859,Human_Splice_Rec_737873,Human_Splice_Rec_737885,Human_Splice_Rec_737899,Human_Splice_Rec_737913,Human_Splice_Rec_737925,Human_Splice_Rec_737937,Human_Splice_Rec_737947,Human_Splice_Rec_737957,Human_Splice_Rec_737971,Human_Splice_Rec_737979,Human_Splice_Rec_737985,Human_Splice_Rec_737989 RMVar_hsa_circ_2896 58761 RMVar_ID_58761 Human_SNP_ID_266730207 m1A Human chr6 - 10409952 10409952 10409952 CTCCTGCACGGCCCACACGCGCTCAGCTCAGGACTCGGAGACCTCTCGATCCACTCCTTACCTCA CTCCTGCACGGCCCACACGCGCTCAGCTCAGGCCTCGGAGACCTCTCGATCCACTCCTTACCTCA T G TFAP2A Ensembl:ENSG00000137203 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10409871..10410364 26863196 MeRIP-seq:(Medium) rs777729482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8894842,Human_RBP_ID_15579757,Human_RBP_ID_17303995,Human_RBP_ID_27518457 Human_Splice_Rec_737847,Human_Splice_Rec_737859,Human_Splice_Rec_737873,Human_Splice_Rec_737885,Human_Splice_Rec_737899,Human_Splice_Rec_737913,Human_Splice_Rec_737925,Human_Splice_Rec_737937,Human_Splice_Rec_737947,Human_Splice_Rec_737957,Human_Splice_Rec_737971,Human_Splice_Rec_737979,Human_Splice_Rec_737985,Human_Splice_Rec_737989 RMVar_hsa_circ_2896 58762 RMVar_ID_58762 Human_SNP_ID_266730219 m1A Human chr6 + 10409980 10409980 10409980 CGAGTCCTGAGCTGAGCGCGTGTGGGCCGTGCAGGAGGTCCTCGTGCCGCCTGTAGTCCCTGCGA CGAGTCCTGAGCTGAGCGCGTGTGGGCCGTGCGGGAGGTCCTCGTGCCGCCTGTAGTCCCTGCGA A G TFAP2A-AS1 Ensembl:ENSG00000229950 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:10409930..10410905 32194978 MeRIP-seq:(Medium) rs968299826 Functional Loss SNV dbSNP153 33..33 33 - - - 58763 RMVar_ID_58763 Human_SNP_ID_266730239 m1A Human chr6 - 10410031 10410031 10410031 GCTCCTGCACACGCACCGGGGGCTGCCTCACCAGCTGTCGGGCCTGGATCCTCGCAGGGACTACA GCTCCTGCACACGCACCGGGGGCTGCCTCACCGGCTGTCGGGCCTGGATCCTCGCAGGGACTACA T C TFAP2A Ensembl:ENSG00000137203 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:10409930..10410031 26863410 MeRIP-seq:(Medium) rs1405134828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4858409,Human_RBP_ID_5427689,Human_RBP_ID_15579763,Human_RBP_ID_18850393 RMVar_hsa_circ_2896 58764 RMVar_ID_58764 Human_SNP_ID_266730316 m1A Human chr6 - 10410226 10410226 10410226 CGCCCCGCCGCTGTCCCACACCCCCAATGCCGACTTCCAGCCCCCATACTTCCCCCCACCCTACC CGCCCCGCCGCTGTCCCACACCCCCAATGCCGCCTTCCAGCCCCCATACTTCCCCCCACCCTACC T G TFAP2A Ensembl:ENSG00000137203 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:10410177..10410350 26863196 MeRIP-seq:(Medium) rs775764363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_649595 RMVar_hsa_circ_2896 58765 RMVar_ID_58765 Human_SNP_ID_266730332 m1A Human chr6 + 10410247 10410247 10410247 GGGGCTGGAAGTCGGCATTGGGGGTGTGGGACAGCGGCGGGGCGCTCGTGTAGGGAGATTGACCT GGGGCTGGAAGTCGGCATTGGGGGTGTGGGACGGCGGCGGGGCGCTCGTGTAGGGAGATTGACCT A G TFAP2A-AS1 Ensembl:ENSG00000229950 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:10410226..10410250 26863196 MeRIP-seq:(Medium) rs751224702 Functional Loss SNV dbSNP153 33..33 33 - - - 58766 RMVar_ID_58766 Human_SNP_ID_266730702 m1A Human chr6 - 10411385 10411385 10411385 CTCTCGCTCTTTTCCATCCCTAAATCGAGTGCATTACCCCCTACCCCAGCCCCCGCTCGACCTCT CTCTCGCTCTTTTCCATCCCTAAATCGAGTGCCTTACCCCCTACCCCAGCCCCCGCTCGACCTCT T G TFAP2A Ensembl:ENSG00000137203 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:10411376..10411475 26863196 MeRIP-seq:(Medium) rs1020846888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15579794 58767 RMVar_ID_58767 Human_SNP_ID_266731012 m1A Human chr6 - 10412250 10412250 10412250 TTTAAAATGTTGCCCCTTCCCTGTGATTCGCCAGACGCCGCGCCGCGGCCCCCCGCGCGCTCGCC TTTAAAATGTTGCCCCTTCCCTGTGATTCGCCGGACGCCGCGCCGCGGCCCCCCGCGCGCTCGCC T C TFAP2A Ensembl:ENSG00000137203 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:10412126..10412355 26863410 MeRIP-seq:(Medium) rs1415138295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4858458,Human_RBP_ID_21224062,Human_RBP_ID_24125572,Human_RBP_ID_24509467 58768 RMVar_ID_58768 Human_SNP_ID_266731044 m1A Human chr6 + 10412340 10412340 10412340 AGAGAAAGAGGCAGAGAGGGAGACCGAAGGAGAGAGCGCAGAGAGGGAGAATGTGTCTGCGTGCG AGAGAAAGAGGCAGAGAGGGAGACCGAAGGAGGGAGCGCAGAGAGGGAGAATGTGTCTGCGTGCG A G TFAP2A-AS1 Ensembl:ENSG00000229950 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:10411901..10412675 26863196 MeRIP-seq:(Medium) rs1211226953 Functional Loss SNV dbSNP153 33..33 33 - - - 58769 RMVar_ID_58769 Human_SNP_ID_266731925 m1A Human chr6 - 10414991 10414991 10414991 ACCGAGAGGGGCATATCCGTTCACGCCGATCCATGAAAATGCTTTGGAAATTGACGGATAATATC ACCGAGAGGGGCATATCCGTTCACGCCGATCCTTGAAAATGCTTTGGAAATTGACGGATAATATC T A TFAP2A Ensembl:ENSG00000137203 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:10414891..10415193;chr6:10414882..10415692;chr6:10412094..10415245 26863196 MeRIP-seq:(Medium) rs1382984593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18363267 Human_Splice_Rec_737857,Human_Splice_Rec_737895,Human_Splice_Rec_737910,Human_Splice_Rec_737911,Human_Splice_Rec_737923,Human_Splice_Rec_737955,Human_Splice_Rec_737963 58770 RMVar_ID_58770 Human_SNP_ID_266731926 m1A Human chr6 - 10414991 10414991 10414991 ACCGAGAGGGGCATATCCGTTCACGCCGATCCATGAAAATGCTTTGGAAATTGACGGATAATATC ACCGAGAGGGGCATATCCGTTCACGCCGATCCGTGAAAATGCTTTGGAAATTGACGGATAATATC T C TFAP2A Ensembl:ENSG00000137203 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:10414891..10415193;chr6:10414882..10415692;chr6:10412094..10415245 26863196 MeRIP-seq:(Medium) rs1382984593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18363267 Human_Splice_Rec_737857,Human_Splice_Rec_737895,Human_Splice_Rec_737910,Human_Splice_Rec_737911,Human_Splice_Rec_737923,Human_Splice_Rec_737955,Human_Splice_Rec_737963 58771 RMVar_ID_58771 Human_SNP_ID_266732149 m1A Human chr6 - 10415527 10415527 10415527 AGAAGGCATCTCTGGAGAAAAGGAAGCGGAGAAAGAAAGGAAGGGGAATGTGGCGGAATTGGGGT AGAAGGCATCTCTGGAGAAAAGGAAGCGGAGAGAGAAAGGAAGGGGAATGTGGCGGAATTGGGGT T C TFAP2A Ensembl:ENSG00000137203 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:10415476..10415615 26863196 MeRIP-seq:(Medium) rs1181574297 Functional Loss SNV dbSNP153 33..33 33 - - - 58772 RMVar_ID_58772 Human_SNP_ID_266769848 m1A Human chr6 + 10528740 10528738 10528741 GAAAATGCAACCTAGTGGTAAGTGAAGAGGGGAAGAAGAAAGAAAAAGGACCAGAACCGTGAACT GAAAATGCAACCTAGTGGTAAGTGAAGAGGG___GAAGAAAGAAAAAGGACCAGAACCGTGAACT GGAA G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10528689..10528785 26863196 MeRIP-seq:(Medium) rs1213869180 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_360338 58773 RMVar_ID_58773 Human_SNP_ID_266778553 m1A Human chr6 + 10556179 10556179 10556179 GGAGGCAGAGGGAGGAGGGAAGGCTGGGCTTCAGCAACCTGCCACGGGGATTTAAACAAAGGAGG GGAGGCAGAGGGAGGAGGGAAGGCTGGGCTTCGGCAACCTGCCACGGGGATTTAAACAAAGGAGG A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10556145..10556217 26863196 MeRIP-seq:(Medium) rs1354877021 Functional Loss SNV dbSNP153 33..33 33 - - - 58774 RMVar_ID_58774 Human_SNP_ID_266789140 m1A Human chr6 - 10588854 10588842 10588854 CAAACACACATACCCCACACACATACACATACACACCACACACACACCACACACATACACTGCAA CAAACACACATACCCCACACACATACACATAC____________CACCACACACATACACTGCAA GTGTGTGTGGTGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:10588818..10588963 26863196 MeRIP-seq:(Medium) rs1312617721 Functional Loss DEL dbSNP153 33..44 33 - - - 58775 RMVar_ID_58775 Human_SNP_ID_266789147 m1A Human chr6 - 10588854 10588850 10588854 CAAACACACATACCCCACACACATACACATACACACCACACACACACCACACACATACACTGCAA CAAACACACATACCCCACACACATACACATAC____CACACACACACCACACACATACACTGCAA GGTGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:10588818..10588963 26863196 MeRIP-seq:(Medium) rs1378698051 Functional Loss DEL dbSNP153 33..36 33 - - - 58776 RMVar_ID_58776 Human_SNP_ID_266789292 m1A Human chr6 - 10589028 10589028 10589028 CACCACACACACACCATACACATACCACGCACATACACCACATATACACACCACACACACACCCA CACCACACACACACCATACACATACCACGCACGTACACCACATATACACACCACACACACACCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:10588804..10589060 26863196 MeRIP-seq:(Medium) rs1318035282 Functional Loss SNV dbSNP153 33..33 33 - - - 58777 RMVar_ID_58777 Human_SNP_ID_266789408 m1A Human chr6 - 10589166 10589166 10589166 ATACACACATGACGCACATACACCACACACACACCACACGCACACACACCCACACCACATAACCA ATACACACATGACGCACATACACCACACACACCCCACACGCACACACACCCACACCACATAACCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:10589118..10589231 26863196 MeRIP-seq:(Medium) rs146409550 Functional Loss SNV dbSNP153 33..33 33 - - - 58778 RMVar_ID_58778 Human_SNP_ID_266816675 m1A Human chr6 + 10694539 10694539 10694539 GAAAGCCTCGTTCCGCTGGTCCCTGAACAAAAACTCCTACCCTACTAGTACACAGCCCACAACAA GAAAGCCTCGTTCCGCTGGTCCCTGAACAAAATCTCCTACCCTACTAGTACACAGCCCACAACAA A T RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10694500..10694575 26863196 MeRIP-seq:(Medium) rs1421009364 Functional Loss SNV dbSNP153 33..33 33 - - - 58779 RMVar_ID_58779 Human_SNP_ID_266816933 m1A Human chr6 - 10695024 10695024 10695024 CAAGCCTCGGGCTCCGGGTGTACAGCGAACCCAAAGAGGACCTGCTCGTAGCAACCAGCGACCAG CAAGCCTCGGGCTCCGGGTGTACAGCGAACCCGAAGAGGACCTGCTCGTAGCAACCAGCGACCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:10694976..10695058 26863196 MeRIP-seq:(Medium) rs1418066411 Functional Loss SNV dbSNP153 33..33 33 - - - 58780 RMVar_ID_58780 Human_SNP_ID_266820544 m1A Human chr6 + 10709324 10709324 10709324 AAGAAGAAAAGCGGTCAAAACCTAACACAAAGAAACGCGGTTTAACAGGTGACAGTAAGAAAGCA AAGAAGAAAAGCGGTCAAAACCTAACACAAAGGAACGCGGTTTAACAGGTGACAGTAAGAAAGCA A G PAK1IP1 Ensembl:ENSG00000111845 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:10709274..10709411 26863196 MeRIP-seq:(Medium) rs1417396834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2003704 Human_Splice_Rec_738202 RMVar_hsa_circ_110872,RMVar_hsa_circ_237105 58781 RMVar_ID_58781 Human_SNP_ID_266820562 m1A Human chr6 + 10709357 10709357 10709357 AACGCGGTTTAACAGGTGACAGTAAGAAAGCAACAAAAGAAAGTGGCCTGATATCAACCAAGAAG AACGCGGTTTAACAGGTGACAGTAAGAAAGCAGCAAAAGAAAGTGGCCTGATATCAACCAAGAAG A G PAK1IP1 Ensembl:ENSG00000111845 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10709306..10709398 26863196 MeRIP-seq:(Medium) rs147259600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1661446,Human_RBP_ID_2003704,Human_RBP_ID_3786592 Human_miRNA_ID_2068433 RMVar_hsa_circ_110872,RMVar_hsa_circ_237105 58782 RMVar_ID_58782 Human_SNP_ID_266826096 m1A Human chr6 - 10725012 10725012 10725012 ACCCTACCTGCTTTTACATAGCCAATGATCCCACCAGAAGCAACCAGTGCTGCGTAGCCAAAGCC ACCCTACCTGCTTTTACATAGCCAATGATCCCCCCAGAAGCAACCAGTGCTGCGTAGCCAAAGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:10724918..10725086 26863196 MeRIP-seq:(Medium) rs1042507896 Functional Loss SNV dbSNP153 33..33 33 - - - 58783 RMVar_ID_58783 Human_SNP_ID_266832256 m1A Human chr6 - 10747864 10747864 10747864 AAGACCTGCACCGACCTGCCGAAGGCCCGCGGAGTCCACTACGGAGCGCAAGCCGCGGGACACAG AAGACCTGCACCGACCTGCCGAAGGCCCGCGGGGTCCACTACGGAGCGCAAGCCGCGGGACACAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:10747821..10747924 26863196 MeRIP-seq:(Medium) rs1159627531 Functional Loss SNV dbSNP153 33..33 33 - - - 58784 RMVar_ID_58784 Human_SNP_ID_266918653 m1A Human chr6 - 11094271 11094255 11094271 GAAGGGCAGTCGGCTCGGGGCGGCTGGCGCGGACGGCGGTGAGCGCGGGCGGCGGCGCGTCCTGC GAAGGGCAGTCGGCTCGGGGCGGCTGGCGCGG________________GCGGCGGCGCGTCCTGC CCCGCGCTCACCGCCGT C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:11094151..11094400 26863410 MeRIP-seq:(Medium) rs1279931500 Functional Loss DEL dbSNP153 33..48 33 - - - 58785 RMVar_ID_58785 Human_SNP_ID_267025101 m1A Human chr6 - 11537601 11537601 11537601 CCCCCGCTCCCCGCGACCCGCCGCCCTCCAACAGCCGGTCGGCCCCAAAGCCCTCCTTCTCGCTC CCCCCGCTCCCCGCGACCCGCCGCCCTCCAACTGCCGGTCGGCCCCAAAGCCCTCCTTCTCGCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:11537550..11537932 26863196 MeRIP-seq:(Medium) rs1056589475 Functional Loss SNV dbSNP153 33..33 33 - - - 58786 RMVar_ID_58786 Human_SNP_ID_267025102 m1A Human chr6 - 11537601 11537601 11537601 CCCCCGCTCCCCGCGACCCGCCGCCCTCCAACAGCCGGTCGGCCCCAAAGCCCTCCTTCTCGCTC CCCCCGCTCCCCGCGACCCGCCGCCCTCCAACCGCCGGTCGGCCCCAAAGCCCTCCTTCTCGCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:11537550..11537932 26863196 MeRIP-seq:(Medium) rs1056589475 Functional Loss SNV dbSNP153 33..33 33 - - - 58787 RMVar_ID_58787 Human_SNP_ID_267025124 m1A Human chr6 + 11537647 11537647 11537647 GGGTCGCGGGGAGCGGGGGAGTGAGCATGCGCAGCGGCTCCGGGGAGCGCAGGGGAGGAGGGGCC GGGTCGCGGGGAGCGGGGGAGTGAGCATGCGCGGCGGCTCCGGGGAGCGCAGGGGAGGAGGGGCC A G lnc-TMEM170B-3,lnc-TMEM170B-3:2 RNACentral:URS00008BF818,RNACentral:URS00008BA316 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:11537561..11537734 26863196 MeRIP-seq:(Medium) rs932061411 Functional Loss SNV dbSNP153 33..33 33 - - - 58788 RMVar_ID_58788 Human_SNP_ID_267137750 m1A Human chr6 + 12012376 12012376 12012376 GGGCGGCGGCAGGGTGGCGGACGGAGCGGGGGACCGGGGAGCGGCGGCCGCCGGAGGAGGTTATG GGGCGGCGGCAGGGTGGCGGACGGAGCGGGGGGCCGGGGAGCGGCGGCCGCCGGAGGAGGTTATG A G HIVEP1 Ensembl:ENSG00000095951 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:12012330..12012557 26863196 MeRIP-seq:(Medium) rs1317043329 Functional Loss SNV dbSNP153 33..33 33 - - - 58789 RMVar_ID_58789 Human_SNP_ID_267233962 m1A Human chr6 + 12399543 12399543 12399543 CATTACTTGATTTCAAACTATATTGTTAGGCCATAATCACCAAAACAGCATGGGACTCGTACAAA CATTACTTGATTTCAAACTATATTGTTAGGCCGTAATCACCAAAACAGCATGGGACTCGTACAAA A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:12399475..12399566 26863410 MeRIP-seq:(Medium) rs1192769392 Functional Loss SNV dbSNP153 33..33 33 - - - 58790 RMVar_ID_58790 Human_SNP_ID_267453930 m1A Human chr6 + 13328416 13328416 13328416 GCAGGCGGGCACCGTTGGGGCCCAGGGCCAGGAGGGACGAGTCCTGCGGGAAGGAGGGAGGCGGC GCAGGCGGGCACCGTTGGGGCCCAGGGCCAGGGGGGACGAGTCCTGCGGGAAGGAGGGAGGCGGC A G RF00017-4500 RNACentral:URS000099DB47 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:13328365..13328482 26863196 MeRIP-seq:(Medium) rs1323480385 Functional Loss SNV dbSNP153 33..33 33 - - - 58791 RMVar_ID_58791 Human_SNP_ID_267453950 m1A Human chr6 - 13328457 13328457 13328457 TCCCGGGCCGTCTGGGCGCGCGCGGGTGTCCCAGGTACCCCGCCGCCTCCCTCCTTCCCGCAGGA TCCCGGGCCGTCTGGGCGCGCGCGGGTGTCCCGGGTACCCCGCCGCCTCCCTCCTTCCCGCAGGA T C TBC1D7 Ensembl:ENSG00000145979 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:13328355..13328522 26863410 MeRIP-seq:(Medium) rs556652298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4864544 Human_Splice_Rec_739307,Human_Splice_Rec_739321,Human_Splice_Rec_739345,Human_Splice_Rec_739355,Human_Splice_Rec_739401,Human_Splice_Rec_739457 58792 RMVar_ID_58792 Human_SNP_ID_267453951 m1A Human chr6 - 13328457 13328457 13328457 TCCCGGGCCGTCTGGGCGCGCGCGGGTGTCCCAGGTACCCCGCCGCCTCCCTCCTTCCCGCAGGA TCCCGGGCCGTCTGGGCGCGCGCGGGTGTCCCCGGTACCCCGCCGCCTCCCTCCTTCCCGCAGGA T G TBC1D7 Ensembl:ENSG00000145979 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:13328355..13328522 26863410 MeRIP-seq:(Medium) rs556652298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4864544 Human_Splice_Rec_739307,Human_Splice_Rec_739321,Human_Splice_Rec_739345,Human_Splice_Rec_739355,Human_Splice_Rec_739401,Human_Splice_Rec_739457 58793 RMVar_ID_58793 Human_SNP_ID_267492296 m1A Human chr6 - 13487234 13487234 13487234 GAGCCGGCCATGGAGCGGCCTTGGCGGGGCGCACGCAGCGGACTGGCGCTGCCGCGGGAGCGCAG GAGCCGGCCATGGAGCGGCCTTGGCGGGGCGCTCGCAGCGGACTGGCGCTGCCGCGGGAGCGCAG T A GFOD1 Ensembl:ENSG00000145990 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13487191..13487348 26863196 MeRIP-seq:(Medium) rs1433991808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18064552 58794 RMVar_ID_58794 Human_SNP_ID_267492354 m1A Human chr6 - 13487427 13487427 13487427 GCATCCTTAGCCGGCCTCCTGGCGGCCGCGGGATTATTTCATTCCCAACGGAGAGCTAGGAAGAA GCATCCTTAGCCGGCCTCCTGGCGGCCGCGGGGTTATTTCATTCCCAACGGAGAGCTAGGAAGAA T C GFOD1 Ensembl:ENSG00000145990 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:13487388..13487587 26863196 MeRIP-seq:(Medium) rs1004984746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18064554 58795 RMVar_ID_58795 Human_SNP_ID_267492360 m1A Human chr6 - 13487457 13487457 13487457 TCGGGATCCCAGTCCGGCGCGCTCCGGGCCGCATCCTTAGCCGGCCTCCTGGCGGCCGCGGGATT TCGGGATCCCAGTCCGGCGCGCTCCGGGCCGCCTCCTTAGCCGGCCTCCTGGCGGCCGCGGGATT T G GFOD1 Ensembl:ENSG00000145990 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13487414..13487585 26863196 MeRIP-seq:(Medium) rs927453808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4864853,Human_RBP_ID_9188173 58796 RMVar_ID_58796 Human_SNP_ID_267526177 m1A Human chr6 + 13615373 13615373 13615373 TCTAGCGCTGCGTGGGCCATGGTGCAGCTCCGACCGCGAGCGTCTCGCGCCCCGGCGTCGGCGGA TCTAGCGCTGCGTGGGCCATGGTGCAGCTCCGGCCGCGAGCGTCTCGCGCCCCGGCGTCGGCGGA A G NOL7 Ensembl:ENSG00000225921 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:13615326..13615486 26863196 MeRIP-seq:(Medium) rs928171338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82049,Human_RBP_ID_4865049,Human_RBP_ID_9309100,Human_RBP_ID_9399953,Human_RBP_ID_22460400,Human_RBP_ID_23116416,Human_RBP_ID_26353098 58797 RMVar_ID_58797 Human_SNP_ID_267526198 m1A Human chr6 - 13615385 13615385 13615385 TCCACCATCGCCTCCGCCGACGCCGGGGCGCGAGACGCTCGCGGTCGGAGCTGCACCATGGCCCA TCCACCATCGCCTCCGCCGACGCCGGGGCGCGGGACGCTCGCGGTCGGAGCTGCACCATGGCCCA T C RF00017-4503,RF00017-4596 RNACentral:URS0000948B80,RNACentral:URS0000934741 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:13615326..13615775;chr6:13615326..13615750 26863196 MeRIP-seq:(Medium) rs1382984085 Functional Loss SNV dbSNP153 33..33 33 - - - 58798 RMVar_ID_58798 Human_SNP_ID_267526278 m1A Human chr6 + 13615511 13615511 13615511 AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGAAGACGAGGAAGGGGACGATGAGTTTGACGATGA AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGACGACGAGGAAGGGGACGATGAGTTTGACGATGA A C NOL7 Ensembl:ENSG00000225921 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:13615424..13615572 26863410 MeRIP-seq:(Medium) rs545142311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4865061,Human_RBP_ID_9401616,Human_RBP_ID_26353405 58799 RMVar_ID_58799 Human_SNP_ID_267526279 m1A Human chr6 + 13615511 13615511 13615511 AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGAAGACGAGGAAGGGGACGATGAGTTTGACGATGA AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGAGGACGAGGAAGGGGACGATGAGTTTGACGATGA A G NOL7 Ensembl:ENSG00000225921 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:13615424..13615572 26863410 MeRIP-seq:(Medium) rs545142311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4865061,Human_RBP_ID_9401616,Human_RBP_ID_26353405 58800 RMVar_ID_58800 Human_SNP_ID_267526301 m1A Human chr6 - 13615563 13615561 13615563 CTCTTCTCTCGCTTCCGCCTGGGCGCTGGCGAAAGTCAGCTCCTCCGGGGCCTCATCGTCAAACT CTCTTCTCTCGCTTCCGCCTGGGCGCTGGCGA__GTCAGCTCCTCCGGGGCCTCATCGTCAAACT CTT C RF00017-4503,RF00017-4596 RNACentral:URS0000948B80,RNACentral:URS0000934741 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:13615376..13616496 32194978 MeRIP-seq:(Medium) rs928015624 Functional Loss DEL dbSNP153 33..34 33 - - - 58801 RMVar_ID_58801 Human_SNP_ID_267526378 m1A Human chr6 - 13615703 13615687 13615704 TTCTCCTTCAGGAGCGTTTTATCCCTGGGAGGAAGGGTGATAAGTCAGCAAAGGGAAGGACAAGC TTCTCCTTCAGGAGCGTTTTATCCCTGGGAG_________________CAAAGGGAAGGACAAGC GCTGACTTATCACCCTTC G RF00017-4503,RF00017-4596 RNACentral:URS0000948B80,RNACentral:URS0000934741 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:13615701..13615775 32194978 MeRIP-seq:(Medium) rs1459657141 Functional Loss DEL dbSNP153 32..48 33 - - - 58802 RMVar_ID_58802 Human_SNP_ID_267526387 m1A Human chr6 - 13615703 13615703 13615703 TTCTCCTTCAGGAGCGTTTTATCCCTGGGAGGAAGGGTGATAAGTCAGCAAAGGGAAGGACAAGC TTCTCCTTCAGGAGCGTTTTATCCCTGGGAGGGAGGGTGATAAGTCAGCAAAGGGAAGGACAAGC T C RF00017-4503,RF00017-4596 RNACentral:URS0000948B80,RNACentral:URS0000934741 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:13615701..13615775 32194978 MeRIP-seq:(Medium) rs759760467 Functional Loss SNV dbSNP153 33..33 33 - - - 58803 RMVar_ID_58803 Human_SNP_ID_267526638 m1A Human chr6 + 13616453 13616453 13616453 TACATGACTTTCTATTAATTTTAAACGTTTTCATTCCAAAAGAAAAGAAAACTCCTTCCAGACAC TACATGACTTTCTATTAATTTTAAACGTTTTCGTTCCAAAAGAAAAGAAAACTCCTTCCAGACAC A G NOL7 Ensembl:ENSG00000225921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13616451..13616500 26863196 MeRIP-seq:(Medium) rs1255308642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22683696 Human_Splice_Rec_739583,Human_Splice_Rec_739597,Human_Splice_Rec_739603 RMVar_hsa_circ_55040 58804 RMVar_ID_58804 Human_SNP_ID_267526639 m1A Human chr6 + 13616453 13616453 13616453 TACATGACTTTCTATTAATTTTAAACGTTTTCATTCCAAAAGAAAAGAAAACTCCTTCCAGACAC TACATGACTTTCTATTAATTTTAAACGTTTTCCTTCCAAAAGAAAAGAAAACTCCTTCCAGACAC A C NOL7 Ensembl:ENSG00000225921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13616451..13616500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22683696 Human_Splice_Rec_739583,Human_Splice_Rec_739597,Human_Splice_Rec_739603 RMVar_hsa_circ_55040 58805 RMVar_ID_58805 Human_SNP_ID_267528507 m1A Human chr6 + 13622056 13622056 13622056 TCCTTCCCCTCTCTCCCCCCTCCCCCACAAAGAAGGCAGGATTTTTGGTTTCTTTTAGGTAATTG TCCTTCCCCTCTCTCCCCCCTCCCCCACAAAGGAGGCAGGATTTTTGGTTTCTTTTAGGTAATTG A G NOL7 Ensembl:ENSG00000225921 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:13621060..13632494 32194978 MeRIP-seq:(Medium) rs1280446747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7545635 58806 RMVar_ID_58806 Human_SNP_ID_267534570 m1A Human chr6 + 13644577 13644577 13644577 TTTTGTATCATGGTCTGCCATTCTCCTTCTCGATCTCCGATAGGAAATCGATCTATCTGTGCCTG TTTTGTATCATGGTCTGCCATTCTCCTTCTCGCTCTCCGATAGGAAATCGATCTATCTGTGCCTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:13642512..13644616 32194978 MeRIP-seq:(Medium) rs917619550 Functional Loss SNV dbSNP153 33..33 33 - - - 58807 RMVar_ID_58807 Human_SNP_ID_267549948 m1A Human chr6 - 13703179 13703179 13703179 CATCAAGGAGATTGGTGTCACAGAAGCTGAGCACGGGAGGGTGCAGTGGCTCACACCTGTAATCC CATCAAGGAGATTGGTGTCACAGAAGCTGAGCTCGGGAGGGTGCAGTGGCTCACACCTGTAATCC T A RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13703176..13703334 26863196 MeRIP-seq:(Medium) rs114264517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15661621 RMVar_hsa_circ_81702,RMVar_hsa_circ_237221 58808 RMVar_ID_58808 Human_SNP_ID_267549949 m1A Human chr6 - 13703179 13703179 13703179 CATCAAGGAGATTGGTGTCACAGAAGCTGAGCACGGGAGGGTGCAGTGGCTCACACCTGTAATCC CATCAAGGAGATTGGTGTCACAGAAGCTGAGCGCGGGAGGGTGCAGTGGCTCACACCTGTAATCC T C RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13703176..13703334 26863196 MeRIP-seq:(Medium) rs114264517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15661621 RMVar_hsa_circ_81702,RMVar_hsa_circ_237221 58809 RMVar_ID_58809 Human_SNP_ID_267549950 m1A Human chr6 - 13703179 13703179 13703179 CATCAAGGAGATTGGTGTCACAGAAGCTGAGCACGGGAGGGTGCAGTGGCTCACACCTGTAATCC CATCAAGGAGATTGGTGTCACAGAAGCTGAGCCCGGGAGGGTGCAGTGGCTCACACCTGTAATCC T G RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13703176..13703334 26863196 MeRIP-seq:(Medium) rs114264517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15661621 RMVar_hsa_circ_81702,RMVar_hsa_circ_237221 58810 RMVar_ID_58810 Human_SNP_ID_267552643 m1A Human chr6 + 13711087 13711087 13711087 GCCGCCGCTGCAACTCCTTCTCCTGCTCGTTCAGGGCCGAGTCCCCGTGAGGGAAGGGGGCCGCG GCCGCCGCTGCAACTCCTTCTCCTGCTCGTTCCGGGCCGAGTCCCCGTGAGGGAAGGGGGCCGCG A C RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:13710964..13711214 32194978 MeRIP-seq:(Medium) rs1372648507 Functional Loss SNV dbSNP153 33..33 33 - - - 58811 RMVar_ID_58811 Human_SNP_ID_267552697 m1A Human chr6 + 13711161 13711161 13711161 CCCGCCACCAGAGCTGGGGTCGGGGCTCCTCCAGCCGGGCCGGGGCCCGCTGCAAGGCCCGGGGG CCCGCCACCAGAGCTGGGGTCGGGGCTCCTCCGGCCGGGCCGGGGCCCGCTGCAAGGCCCGGGGG A G RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:13711114..13711214 32194978 MeRIP-seq:(Medium) rs1320528083 Functional Loss SNV dbSNP153 33..33 33 - - - 58812 RMVar_ID_58812 Human_SNP_ID_267552741 m1A Human chr6 + 13711236 13711236 13711236 CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGAGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGCGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC A C RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr6:13711079..13711357;chr6:13711163..13711564 26863196,26863410 MeRIP-seq:(Medium) rs989477384 Functional Loss SNV dbSNP153 33..33 33 - - - 58813 RMVar_ID_58813 Human_SNP_ID_267552742 m1A Human chr6 + 13711236 13711236 13711236 CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGAGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGGGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC A G RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr6:13711079..13711357;chr6:13711163..13711564 26863196,26863410 MeRIP-seq:(Medium) rs989477384 Functional Loss SNV dbSNP153 33..33 33 - - - 58814 RMVar_ID_58814 Human_SNP_ID_267552927 m1A Human chr6 + 13711520 13711520 13711520 CGGCGGCTGCCCGGACATCCCGGCCGCGACTCAGCCTGCGGCCACCTCCACCTCTTCTCTCCTTC CGGCGGCTGCCCGGACATCCCGGCCGCGACTCCGCCTGCGGCCACCTCCACCTCTTCTCTCCTTC A C RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:13711307..13711837 26863196 MeRIP-seq:(Medium) rs764230886 Functional Loss SNV dbSNP153 33..33 33 - - - 58815 RMVar_ID_58815 Human_SNP_ID_267552928 m1A Human chr6 + 13711520 13711520 13711520 CGGCGGCTGCCCGGACATCCCGGCCGCGACTCAGCCTGCGGCCACCTCCACCTCTTCTCTCCTTC CGGCGGCTGCCCGGACATCCCGGCCGCGACTCGGCCTGCGGCCACCTCCACCTCTTCTCTCCTTC A G RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:13711307..13711837 26863196 MeRIP-seq:(Medium) rs764230886 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 58816 RMVar_ID_58816 Human_SNP_ID_267553006 m1A Human chr6 + 13711674 13711674 13711674 CCCAGGGAGACCGCGGCGGTTGAGGAGCTCGGAGACGCGGGAGTAGGCGGCGGGCCCGGGAGGCC CCCAGGGAGACCGCGGCGGTTGAGGAGCTCGGGGACGCGGGAGTAGGCGGCGGGCCCGGGAGGCC A G RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:13710924..13711850 26863196 MeRIP-seq:(Medium) rs1460123157 Functional Loss SNV dbSNP153 33..33 33 - - - 58817 RMVar_ID_58817 Human_SNP_ID_267576393 m1A Human chr6 - 13789318 13789318 13789318 CTGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGTCTCCTGAGTAGCT CTGCTCACTGCAACCTCTGCCTCCTGGGTTCAGGCGATTCTCCTGCCTCAGTCTCCTGAGTAGCT T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1253873556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7100,RMVar_hsa_circ_109132,RMVar_hsa_circ_331721,RMVar_hsa_circ_237237,RMVar_hsa_circ_62883 58818 RMVar_ID_58818 Human_SNP_ID_267615396 m1A Human chr6 + 13924634 13924634 13924634 TGTGGGGGGGATGGTGGTGCGACGGGAGTTGGAATGTCCAGTGTGGGGAAGCAAAGGAGTGCCTA TGTGGGGGGGATGGTGGTGCGACGGGAGTTGGCATGTCCAGTGTGGGGAAGCAAAGGAGTGCCTA A C RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:13924583..13924833 26863196 MeRIP-seq:(Medium) rs550847396 Functional Loss SNV dbSNP153 33..33 33 - - - 58819 RMVar_ID_58819 Human_SNP_ID_267615397 m1A Human chr6 + 13924634 13924634 13924634 TGTGGGGGGGATGGTGGTGCGACGGGAGTTGGAATGTCCAGTGTGGGGAAGCAAAGGAGTGCCTA TGTGGGGGGGATGGTGGTGCGACGGGAGTTGGTATGTCCAGTGTGGGGAAGCAAAGGAGTGCCTA A T RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:13924583..13924833 26863196 MeRIP-seq:(Medium) rs550847396 Functional Loss SNV dbSNP153 33..33 33 - - - 58820 RMVar_ID_58820 Human_SNP_ID_267615640 m1A Human chr6 + 13925131 13925131 13925131 CCCCGCAGTCCTGGACGGCGCCGGGCCGCCCAAGCGCGCCGAGGAGAGGGGGCGGCAAACTTCGG CCCCGCAGTCCTGGACGGCGCCGGGCCGCCCAGGCGCGCCGAGGAGAGGGGGCGGCAAACTTCGG A G RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:13924888..13925350 26863196 MeRIP-seq:(Medium) rs556461980 Functional Loss SNV dbSNP153 33..33 33 - - - 58821 RMVar_ID_58821 Human_SNP_ID_267615657 m1A Human chr6 + 13925168 13925168 13925168 GCCGAGGAGAGGGGGCGGCAAACTTCGGGCCGAGCGGCGCCGGGGCCCGCGCGCGGAGTCTCCCT GCCGAGGAGAGGGGGCGGCAAACTTCGGGCCGGGCGGCGCCGGGGCCCGCGCGCGGAGTCTCCCT A G RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:13925126..13925292 26863196 MeRIP-seq:(Medium) rs1561771904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22617900 58822 RMVar_ID_58822 Human_SNP_ID_267617052 m1A Human chr6 + 13931022 13931022 13931022 TTATGTTACTTTGGAAAGAGTGGCAGTTGAGGACTGCCTGGTGGAGCAAATTCAGAGTGGCAGGT TTATGTTACTTTGGAAAGAGTGGCAGTTGAGGTCTGCCTGGTGGAGCAAATTCAGAGTGGCAGGT A T RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:13931014..13931124 26863196 MeRIP-seq:(Medium) rs1278630044 Functional Loss SNV dbSNP153 33..33 33 - - - 58823 RMVar_ID_58823 Human_SNP_ID_267617931 m1A Human chr6 + 13934841 13934841 13934841 TACCTTAGATTAAAGGGTAAGGTAACATTTAAATAGGGATTTGAGTGACGAGAAGATTTGATCAA TACCTTAGATTAAAGGGTAAGGTAACATTTAAGTAGGGATTTGAGTGACGAGAAGATTTGATCAA A G RNF182 Ensembl:ENSG00000180537 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13934839..13934918 26863196 MeRIP-seq:(Medium) rs1332458054 Functional Loss SNV dbSNP153 33..33 33 - - - 58824 RMVar_ID_58824 Human_SNP_ID_267664414 m1A Human chr6 - 14117837 14117837 14117837 ACAGGCGCTCGCGAGCCCTACCGCAGCTCAGGAGCAGAAGCTGGAGGCCGCGCGACATGGCTGGA ACAGGCGCTCGCGAGCCCTACCGCAGCTCAGGCGCAGAAGCTGGAGGCCGCGCGACATGGCTGGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:14117786..14117925 26863196 MeRIP-seq:(Medium) rs752769812 Functional Loss SNV dbSNP153 33..33 33 - - - 58825 RMVar_ID_58825 Human_SNP_ID_267664540 m1A Human chr6 - 14118015 14118015 14118015 GTAGGGAACCTGCGGATCCCAGGGGGCGGTGCAGGGCAAGTCCACATCTTCGGAGCAAGCCACCT GTAGGGAACCTGCGGATCCCAGGGGGCGGTGCTGGGCAAGTCCACATCTTCGGAGCAAGCCACCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:14117776..14118106 26863196 MeRIP-seq:(Medium) rs748196931 Functional Loss SNV dbSNP153 33..33 33 - - - 58826 RMVar_ID_58826 Human_SNP_ID_267685648 m1A Human chr6 + 14211101 14211101 14211101 CGGGCCCCTTACCTCCCGCGCGCGGCGGGCGCACGCACCACCTGACTCGCGTTCTCATTGGCTGC CGGGCCCCTTACCTCCCGCGCGCGGCGGGCGCGCGCACCACCTGACTCGCGTTCTCATTGGCTGC A G AL353152.2 Ensembl:ENSG00000286281 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:14210953..14211114 26863196 MeRIP-seq:(Medium) rs1002199982 Functional Loss SNV dbSNP153 33..33 33 - - - 58827 RMVar_ID_58827 Human_SNP_ID_704152406 m1A Human chr22 - 40007397 40007397 40007397 GAGAGGAGGAGGACAGGAGGAAGAGGAGGAGGAGAGGAAGAGGAGAGGAGGAGGAGAGGAAGAGG GAGAGGAGGAGGACAGGAGGAAGAGGAGGAGGGGAGGAAGAGGAGAGGAGGAGGAGAGGAAGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:40007329..40007426 26863196 MeRIP-seq:(Medium) rs1410971654 Functional Loss SNV dbSNP153 33..33 33 - - - 58828 RMVar_ID_58828 Human_SNP_ID_704172068 m1A Human chr22 - 40083640 40083640 40083640 AATCTTGCAATTCTCCCCTTTTTCCTCCACCAACCTTCACTCACTGTTTCCTGGATCACCCCCAC AATCTTGCAATTCTCCCCTTTTTCCTCCACCAGCCTTCACTCACTGTTTCCTGGATCACCCCCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40083624..40083770 26863196 MeRIP-seq:(Medium) rs1467416655 Functional Loss SNV dbSNP153 33..33 33 - - - 58829 RMVar_ID_58829 Human_SNP_ID_704183520 m1A Human chr22 + 40132381 40132381 40132381 GTGTGAAACTCCATCTCAATAAAGACGAGACGAGACGGGACGGGACGGGACGGAGCCAGGAGGCA GTGTGAAACTCCATCTCAATAAAGACGAGACGGGACGGGACGGGACGGGACGGAGCCAGGAGGCA A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40132351..40132511 26863196 MeRIP-seq:(Medium) rs184714953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99177,RMVar_hsa_circ_272040,RMVar_hsa_circ_353382,RMVar_hsa_circ_51529,RMVar_hsa_circ_76525,RMVar_hsa_circ_214424,RMVar_hsa_circ_214425,RMVar_hsa_circ_214423,RMVar_hsa_circ_214426,RMVar_hsa_circ_109850 58830 RMVar_ID_58830 Human_SNP_ID_704198442 m1A Human chr22 + 40185981 40185981 40185981 TACTGAATTGGAGAATTTGGTGGGACTTGGCAATGGAACTGGTTAGCAGGCAGCTGGCAGTGTGG TACTGAATTGGAGAATTTGGTGGGACTTGGCAGTGGAACTGGTTAGCAGGCAGCTGGCAGTGTGG A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40185973..40186203 26863196 MeRIP-seq:(Medium) rs979102386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14492324 RMVar_hsa_circ_99177,RMVar_hsa_circ_353382,RMVar_hsa_circ_51529,RMVar_hsa_circ_76525,RMVar_hsa_circ_214424,RMVar_hsa_circ_214425,RMVar_hsa_circ_214426,RMVar_hsa_circ_109850 58831 RMVar_ID_58831 Human_SNP_ID_704213534 m1A Human chr22 + 40246064 40246064 40246064 GGGAAGAACAGTTAATGGAAGACAAGAAAAGGAAGAAAGAGGATAAAAAGAAAAAAGAAGCCACT GGGAAGAACAGTTAATGGAAGACAAGAAAAGGGAGAAAGAGGATAAAAAGAAAAAAGAAGCCACT A G TNRC6B Ensembl:ENSG00000100354 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40245968..40246068 26863196 MeRIP-seq:(Medium) rs909991060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931051,Human_RBP_ID_3962418,Human_RBP_ID_5529945,Human_RBP_ID_9348403,Human_RBP_ID_19009263,Human_RBP_ID_24547072,Human_RBP_ID_26345442,Human_RBP_ID_27821325 Human_Splice_Rec_2168800,Human_Splice_Rec_2168801,Human_Splice_Rec_2168846,Human_Splice_Rec_2168847,Human_Splice_Rec_2168886,Human_Splice_Rec_2168888,Human_Splice_Rec_2168889,Human_Splice_Rec_2168932,Human_Splice_Rec_2168933 RMVar_hsa_circ_99177,RMVar_hsa_circ_353382,RMVar_hsa_circ_51529,RMVar_hsa_circ_76525,RMVar_hsa_circ_214424,RMVar_hsa_circ_214425,RMVar_hsa_circ_356504,RMVar_hsa_circ_214426,RMVar_hsa_circ_109850,RMVar_hsa_circ_365437,RMVar_hsa_circ_365919,RMVar_hsa_circ_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_17439 58832 RMVar_ID_58832 Human_SNP_ID_704217509 m1A Human chr22 + 40262082 40262082 40262082 CCACCGTCCTGCATGCTCCTTGGGGGTGGGGCAGGGCCTCCTCCCTGCACAGCACCTGGAGCAAA CCACCGTCCTGCATGCTCCTTGGGGGTGGGGCTGGGCCTCCTCCCTGCACAGCACCTGGAGCAAA A T TNRC6B Ensembl:ENSG00000100354 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:40261991..40262093 32194978 MeRIP-seq:(Medium) rs1363457500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931783,Human_RBP_ID_8235711,Human_RBP_ID_9392373,Human_RBP_ID_21985170,Human_RBP_ID_22086580,Human_RBP_ID_26345444 Human_Splice_Rec_2168805,Human_Splice_Rec_2168851,Human_Splice_Rec_2168893,Human_Splice_Rec_2168937 Human_miRNA_ID_235234,Human_miRNA_ID_1366725,Human_miRNA_ID_1371092,Human_miRNA_ID_2030925,Human_miRNA_ID_2030926,Human_miRNA_ID_2691354,Human_miRNA_ID_2691355,Human_miRNA_ID_2694697,Human_miRNA_ID_2694698 RMVar_hsa_circ_2242,RMVar_hsa_circ_99177,RMVar_hsa_circ_51529,RMVar_hsa_circ_76525,RMVar_hsa_circ_214424,RMVar_hsa_circ_214425,RMVar_hsa_circ_119237,RMVar_hsa_circ_356504,RMVar_hsa_circ_214426,RMVar_hsa_circ_109850,RMVar_hsa_circ_365437,RMVar_hsa_circ_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_17439,RMVar_hsa_circ_299115,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_367405,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_214428,RMVar_hsa_circ_214429 58833 RMVar_ID_58833 Human_SNP_ID_704218723 m1A Human chr22 + 40266219 40266219 40266219 TGGGAGAGCGCTGCCACACAGACCAAGAACTCAGGGGGCTGGGGAGATGCACCCAGCCAAAGCAA TGGGAGAGCGCTGCCACACAGACCAAGAACTCGGGGGGCTGGGGAGATGCACCCAGCCAAAGCAA A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40266173..40266272 26863196 MeRIP-seq:(Medium) rs1182302095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3963295,Human_RBP_ID_9393002,Human_RBP_ID_17986706,Human_RBP_ID_18789707,Human_RBP_ID_22724471,Human_RBP_ID_26345448 Human_miRNA_ID_1974046,Human_miRNA_ID_1976226,Human_miRNA_ID_2258801,Human_miRNA_ID_2614014 RMVar_hsa_circ_2242,RMVar_hsa_circ_99177,RMVar_hsa_circ_51529,RMVar_hsa_circ_214425,RMVar_hsa_circ_119237,RMVar_hsa_circ_356504,RMVar_hsa_circ_365437,RMVar_hsa_circ_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_367405,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_214429,RMVar_hsa_circ_331155,RMVar_hsa_circ_333281,RMVar_hsa_circ_214430 58834 RMVar_ID_58834 Human_SNP_ID_704218724 m1A Human chr22 + 40266219 40266219 40266219 TGGGAGAGCGCTGCCACACAGACCAAGAACTCAGGGGGCTGGGGAGATGCACCCAGCCAAAGCAA TGGGAGAGCGCTGCCACACAGACCAAGAACTCTGGGGGCTGGGGAGATGCACCCAGCCAAAGCAA A T TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40266173..40266272 26863196 MeRIP-seq:(Medium) rs1182302095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3963295,Human_RBP_ID_9393002,Human_RBP_ID_17986706,Human_RBP_ID_18789707,Human_RBP_ID_22724471,Human_RBP_ID_26345448 Human_miRNA_ID_1974046,Human_miRNA_ID_1976226,Human_miRNA_ID_2258801,Human_miRNA_ID_2614014 RMVar_hsa_circ_2242,RMVar_hsa_circ_99177,RMVar_hsa_circ_51529,RMVar_hsa_circ_214425,RMVar_hsa_circ_119237,RMVar_hsa_circ_356504,RMVar_hsa_circ_365437,RMVar_hsa_circ_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_367405,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_214429,RMVar_hsa_circ_331155,RMVar_hsa_circ_333281,RMVar_hsa_circ_214430 58835 RMVar_ID_58835 Human_SNP_ID_704218845 m1A Human chr22 - 40266536 40266536 40266536 TTTCATTCTGCCCTCCTTCACCCCACCCAGACACAGGTTTACTTGCAGAACTTTCCCAATTGCTG TTTCATTCTGCCCTCCTTCACCCCACCCAGACGCAGGTTTACTTGCAGAACTTTCCCAATTGCTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:40266428..40266780 26863196 MeRIP-seq:(Medium) rs201052764 Functional Loss SNV dbSNP153 33..33 33 - - - 58836 RMVar_ID_58836 Human_SNP_ID_704245264 m1A Human chr22 + 40366099 40366099 40366099 AGGCAGTGGTGAGAGACACAGACCGGGGAGGGAGAGGAGGTTAAGCTCTTGGTGGCTACTTGAAG AGGCAGTGGTGAGAGACACAGACCGGGGAGGGTGAGGAGGTTAAGCTCTTGGTGGCTACTTGAAG A T AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40366092..40366165 26863196 MeRIP-seq:(Medium) rs1041443543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_40538,RMVar_hsa_circ_214453,RMVar_hsa_circ_281970,RMVar_hsa_circ_101403,RMVar_hsa_circ_330350,RMVar_hsa_circ_214452,RMVar_hsa_circ_86469,RMVar_hsa_circ_308317,RMVar_hsa_circ_214463,RMVar_hsa_circ_214462,RMVar_hsa_circ_364944,RMVar_hsa_circ_27433,RMVar_hsa_circ_49366,RMVar_hsa_circ_214471,RMVar_hsa_circ_271539 58837 RMVar_ID_58837 Human_SNP_ID_704250798 m1A Human chr22 + 40388561 40388561 40388561 AATCAAGTTAACAAATTTGGACTTTAAAGCAAAGGGAAGGTTTTAAAGATGGGAGGGAAATGATC AATCAAGTTAACAAATTTGGACTTTAAAGCAAGGGGAAGGTTTTAAAGATGGGAGGGAAATGATC A G AL022238.4,ADSL,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000239900,Ensembl:ENSG00000100359 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40388558..40388730 26863196 MeRIP-seq:(Medium) rs1259603030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422 58838 RMVar_ID_58838 Human_SNP_ID_704253768 m1A Human chr22 + 40400775 40400775 40400775 AAGATAGCAGGATAGGAGACTTCTAAGATTGGAGCTGCAGAAGACTTGCCAGCCCACCAGCACAA AAGATAGCAGGATAGGAGACTTCTAAGATTGGCGCTGCAGAAGACTTGCCAGCCCACCAGCACAA A C AL022238.4,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000100359 Protein coding,Protein coding 3'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40400676..40400869 26863196 MeRIP-seq:(Medium) rs1434087850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65339,Human_RBP_ID_931067,Human_RBP_ID_1943252,Human_RBP_ID_3673430,Human_RBP_ID_3962430,Human_RBP_ID_4699587,Human_RBP_ID_9393008,Human_RBP_ID_14495317,Human_RBP_ID_18423912,Human_RBP_ID_19008099,Human_RBP_ID_23016215,Human_RBP_ID_27821338 Human_Splice_Rec_2169332,Human_Splice_Rec_2169333,Human_Splice_Rec_2169370,Human_Splice_Rec_2169371,Human_Splice_Rec_2169384,Human_Splice_Rec_2169385,Human_Splice_Rec_2169426,Human_Splice_Rec_2169427 RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_35483,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422,RMVar_hsa_circ_60596 58839 RMVar_ID_58839 Human_SNP_ID_704257055 m1A Human chr22 + 40409356 40409356 40409356 GGTCCTTCCTGCGCAGCCCGGGCTGGGTCCAGATCAAGTGTGAGCTCCGGTGAGGACCTTACTGG GGTCCTTCCTGCGCAGCCCGGGCTGGGTCCAGCTCAAGTGTGAGCTCCGGTGAGGACCTTACTGG A C AL022238.4,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000100359 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:40409202..40409991 32194978 MeRIP-seq:(Medium) rs201201598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2169365,Human_Splice_Rec_2169421,Human_Splice_Rec_2169459,Human_Splice_Rec_2169477,Human_Splice_Rec_2169529,Human_Splice_Rec_2169537,Human_Splice_Rec_2169545,Human_Splice_Rec_2169550,Human_Splice_Rec_2169551 RMVar_hsa_circ_109000,RMVar_hsa_circ_109973,RMVar_hsa_circ_214475,RMVar_hsa_circ_214477 58840 RMVar_ID_58840 Human_SNP_ID_704258093 m1A Human chr22 + 40411498 40411498 40411498 GTGCTGAGGGGGGCTAGGCTCAGCACGGGACCACCTGACGACAGCTCCAGCCAGTCCATGCTGTC GTGCTGAGGGGGGCTAGGCTCAGCACGGGACCCCCTGACGACAGCTCCAGCCAGTCCATGCTGTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:40411451..40411550 26863196 MeRIP-seq:(Medium) rs958529146 Functional Loss SNV dbSNP153 33..33 33 - - - 58841 RMVar_ID_58841 Human_SNP_ID_704259435 m1A Human chr22 - 40415516 40415516 40415516 TTCTCTTTGAGTGTCTCAGTGGCTTCAGGAGGAGGAGGAGCGGCTGAGGGGTGCAGGCAAAGTGG TTCTCTTTGAGTGTCTCAGTGGCTTCAGGAGGTGGAGGAGCGGCTGAGGGGTGCAGGCAAAGTGG T A MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40415512..40415904 26863196 MeRIP-seq:(Medium) rs1016499895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106869,RMVar_hsa_circ_214483 58842 RMVar_ID_58842 Human_SNP_ID_704259696 m1A Human chr22 + 40416474 40416474 40416474 GGAGCCAAAGCCACCCTGCCCTGGTGCCCAGGAGGCCACGCATGATCTGGCCATGAAGGCCTTCT GGAGCCAAAGCCACCCTGCCCTGGTGCCCAGGCGGCCACGCATGATCTGGCCATGAAGGCCTTCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40416467..40416632 26863196 MeRIP-seq:(Medium) rs947391225 Functional Loss SNV dbSNP153 33..33 33 - - - 58843 RMVar_ID_58843 Human_SNP_ID_704260016 m1A Human chr22 + 40417475 40417450 40417475 GTCCATCTGGGCAGAGGGGGCAGGCGCTGGAGAGCCAGGCTGGGACGAGGGCTGGACAGGAGAGC GTCCATCT_________________________GCCAGGCTGGGACGAGGGCTGGACAGGAGAGC TGGGCAGAGGGGGCAGGCGCTGGAGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40417424..40417523 26863196 MeRIP-seq:(Medium) rs1464519404 Functional Loss DEL dbSNP153 9..33 33 - - - 58844 RMVar_ID_58844 Human_SNP_ID_704260035 m1A Human chr22 + 40417475 40417475 40417475 GTCCATCTGGGCAGAGGGGGCAGGCGCTGGAGAGCCAGGCTGGGACGAGGGCTGGACAGGAGAGC GTCCATCTGGGCAGAGGGGGCAGGCGCTGGAGGGCCAGGCTGGGACGAGGGCTGGACAGGAGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40417424..40417523 26863196 MeRIP-seq:(Medium) rs775532649 Functional Loss SNV dbSNP153 33..33 33 - - - 58845 RMVar_ID_58845 Human_SNP_ID_704260428 m1A Human chr22 + 40418492 40418492 40418492 TGATGAGGGTGGGAGGTGCAACCCCCTTGATGAGGCTGGGGCCCTGAGGCCCCAGAAGCAACTGG TGATGAGGGTGGGAGGTGCAACCCCCTTGATGGGGCTGGGGCCCTGAGGCCCCAGAAGCAACTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:40418441..40418601 32194978 MeRIP-seq:(Medium) rs1208635677 Functional Loss SNV dbSNP153 33..33 33 - - - 58846 RMVar_ID_58846 Human_SNP_ID_704260638 m1A Human chr22 - 40418840 40418840 40418840 CAAGGACCAGATGCTGCAGGAGAAAGACAAGCAGATCGAGGCGCTGACGCGCATGCTCCGGCAGA CAAGGACCAGATGCTGCAGGAGAAAGACAAGCCGATCGAGGCGCTGACGCGCATGCTCCGGCAGA T G MRTFA Ensembl:ENSG00000196588 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40418790..40418932 26863196 MeRIP-seq:(Medium) rs747812349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_106869,RMVar_hsa_circ_116331,RMVar_hsa_circ_214483,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_268253 58847 RMVar_ID_58847 Human_SNP_ID_704260857 m1A Human chr22 - 40419169 40419169 40419169 GCCCGGCTGAGCACGGGGCCAGCCCTGGTGGCAGCAGGCCTGGCTCCAGCTGAGGTGGTGGTGGC GCCCGGCTGAGCACGGGGCCAGCCCTGGTGGCGGCAGGCCTGGCTCCAGCTGAGGTGGTGGTGGC T C MRTFA Ensembl:ENSG00000196588 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:40419126..40419350 26863196 MeRIP-seq:(Medium) rs1228170231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_106869,RMVar_hsa_circ_116331,RMVar_hsa_circ_214483,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_268253 58848 RMVar_ID_58848 Human_SNP_ID_704261496 m1A Human chr22 - 40420952 40420952 40420952 GGACAGGGGGGCACCCCCCATGGACTCATCCTACGCCAAGATCCTGCAGCAGCAGCAGCTCTTCC GGACAGGGGGGCACCCCCCATGGACTCATCCTCCGCCAAGATCCTGCAGCAGCAGCAGCTCTTCC T G MRTFA Ensembl:ENSG00000196588 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40420901..40421035 26863196 MeRIP-seq:(Medium) rs771544805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8864030 RMVar_hsa_circ_80394,RMVar_hsa_circ_106869,RMVar_hsa_circ_116331,RMVar_hsa_circ_214483,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_265656,RMVar_hsa_circ_214486,RMVar_hsa_circ_268253,RMVar_hsa_circ_41506,RMVar_hsa_circ_50679 58849 RMVar_ID_58849 Human_SNP_ID_704261502 m1A Human chr22 + 40420964 40420964 40420964 GCTGCTGCAGGATCTTGGCGTAGGATGAGTCCATGGGGGGTGCCCCCCTGTCCTGCTTCTGGTCC GCTGCTGCAGGATCTTGGCGTAGGATGAGTCCGTGGGGGGTGCCCCCCTGTCCTGCTTCTGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40420919..40421047 26863196 MeRIP-seq:(Medium) rs1417849237 Functional Loss SNV dbSNP153 33..33 33 - - - 58850 RMVar_ID_58850 Human_SNP_ID_704272128 m1A Human chr22 - 40461899 40461899 40461899 CCAGTGTGGCTGGGGCATGGTGGAGAGAGAGAAGGGGCAAGTGAAGATGGGTAAGGTGGGCAGGG CCAGTGTGGCTGGGGCATGGTGGAGAGAGAGAGGGGGCAAGTGAAGATGGGTAAGGTGGGCAGGG T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40461894..40462065 26863196 MeRIP-seq:(Medium) rs1019363711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_116331,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_40867,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_337554,RMVar_hsa_circ_214492 58851 RMVar_ID_58851 Human_SNP_ID_704272923 m1A Human chr22 - 40464896 40464896 40464896 TGGCAGGGTAAAATTGATAAGAGGGGAGTGTGAGTGTGAGGAGGTAGAGTTGAAGTTGGCCCAGA TGGCAGGGTAAAATTGATAAGAGGGGAGTGTGGGTGTGAGGAGGTAGAGTTGAAGTTGGCCCAGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40464894..40465107 26863196 MeRIP-seq:(Medium) rs1164944341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_116331,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_40867,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_45826,RMVar_hsa_circ_320252,RMVar_hsa_circ_347051,RMVar_hsa_circ_214493 58852 RMVar_ID_58852 Human_SNP_ID_704272932 m1A Human chr22 - 40464939 40464939 40464939 CAAGGACACAGCCAGGGAGCTACCACTGCAGCATGGGAAAACATGGCAGGGTAAAATTGATAAGA CAAGGACACAGCCAGGGAGCTACCACTGCAGCGTGGGAAAACATGGCAGGGTAAAATTGATAAGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40464938..40465095 26863196 MeRIP-seq:(Medium) rs1318531796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_116331,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_40867,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_45826,RMVar_hsa_circ_320252,RMVar_hsa_circ_347051,RMVar_hsa_circ_214493 58853 RMVar_ID_58853 Human_SNP_ID_704292678 m1A Human chr22 - 40540259 40540259 40540259 AACAAGGCCGAAGAGGAGGAGCACAGTGCTCAAGTACACACTACCACCTGTGAAATACTCCTTTC AACAAGGCCGAAGAGGAGGAGCACAGTGCTCAGGTACACACTACCACCTGTGAAATACTCCTTTC T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40540256..40540514 26863196 MeRIP-seq:(Medium) rs150963989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_116331,RMVar_hsa_circ_214484,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_40867,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_320252,RMVar_hsa_circ_347051,RMVar_hsa_circ_214493 58854 RMVar_ID_58854 Human_SNP_ID_704293188 m1A Human chr22 + 40542139 40542139 40542139 CATTTCACATCACTTCCTCCCAAACTCCCTCCACTGATATACTGGTACTCTTCCAGTTCCTTTGT CATTTCACATCACTTCCTCCCAAACTCCCTCCGCTGATATACTGGTACTCTTCCAGTTCCTTTGT A G MRTFA-AS1 RNACentral:URS000078844F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:40542137..40542271;chr22:40542130..40542269 26863196 MeRIP-seq:(Medium) rs989023090 Functional Loss SNV dbSNP153 33..33 33 - - - 58855 RMVar_ID_58855 Human_SNP_ID_704306356 m1A Human chr22 - 40595984 40595984 40595984 ATCAGATTATGAAAGGCTTCAGGGCCAGGGAGATGGGAGAATTATGTGATCCCAGGAGGTTGAGG ATCAGATTATGAAAGGCTTCAGGGCCAGGGAGGTGGGAGAATTATGTGATCCCAGGAGGTTGAGG T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40595982..40596119 26863196 MeRIP-seq:(Medium) rs1187919491 Functional Loss SNV dbSNP153 33..33 33 - - - 58856 RMVar_ID_58856 Human_SNP_ID_704316554 m1A Human chr22 - 40636558 40636558 40636558 CGACTTCTCAGCTCCGTGCGCCCGGGCTGGACAGTGAGCCTCGAGAGGAGACGCGGGCGGCTAGA CGACTTCTCAGCTCCGTGCGCCCGGGCTGGACCGTGAGCCTCGAGAGGAGACGCGGGCGGCTAGA T G MRTFA Ensembl:ENSG00000196588 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:40636526..40636650 26863196 MeRIP-seq:(Medium) rs1287149935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4699731,Human_RBP_ID_18423652 Human_Splice_Rec_2169567,Human_Splice_Rec_2169637,Human_Splice_Rec_2169711,Human_Splice_Rec_2169739,Human_Splice_Rec_2169795,Human_Splice_Rec_2169799,Human_Splice_Rec_2169803,Human_Splice_Rec_2169809 58857 RMVar_ID_58857 Human_SNP_ID_704316585 m1A Human chr22 - 40636640 40636640 40636640 GTGGTGGCCGCGGCGGCGAGAGCGACGGTCCCATCTTTCCCACCCTCTTGGTTGCCGCTGGCCAC GTGGTGGCCGCGGCGGCGAGAGCGACGGTCCCGTCTTTCCCACCCTCTTGGTTGCCGCTGGCCAC T C MRTFA Ensembl:ENSG00000196588 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40636415..40636659 26863196 MeRIP-seq:(Medium) rs969556213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4699740,Human_RBP_ID_5424551,Human_RBP_ID_5446590,Human_RBP_ID_5473201,Human_RBP_ID_5504897,Human_RBP_ID_18423652 58858 RMVar_ID_58858 Human_SNP_ID_704351052 m1A Human chr22 + 40770525 40770525 40770525 TTTAAGAAAGATTTAAATAGAAAACATTACACATGAGAGCAAAATAGTCCATTTCTCTTAAGAAA TTTAAGAAAGATTTAAATAGAAAACATTACACGTGAGAGCAAAATAGTCCATTTCTCTTAAGAAA A G lnc-XPNPEP3-4 RNACentral:URS00008B7943 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:40770476..40770777 32194978 MeRIP-seq:(Medium) rs1480933552 Functional Loss SNV dbSNP153 33..33 33 - - - 58859 RMVar_ID_58859 Human_SNP_ID_704362449 m1A Human chr22 - 40817137 40817137 40817137 GTTGATAAATCCAGTGGTTAATTGAAAAGACCAGTTTTGGTGGAGTGGTGGGGGAAATAGTTGGA GTTGATAAATCCAGTGGTTAATTGAAAAGACCGGTTTTGGTGGAGTGGTGGGGGAAATAGTTGGA T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40817135..40817319 26863196 MeRIP-seq:(Medium) rs1196700512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3673665,Human_RBP_ID_10053474 58860 RMVar_ID_58860 Human_SNP_ID_704362468 m1A Human chr22 + 40817211 40817211 40817211 TCTCAGTTATTTCTCAGTCCTCACCTTACTTGACCCATCAGCAGCATCTGACCCAGCTGGTCTAC TCTCAGTTATTTCTCAGTCCTCACCTTACTTGGCCCATCAGCAGCATCTGACCCAGCTGGTCTAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40817205..40817586 26863196 MeRIP-seq:(Medium) rs938705908 Functional Loss SNV dbSNP153 33..33 33 - - - 58861 RMVar_ID_58861 Human_SNP_ID_704362515 m1A Human chr22 - 40817382 40817382 40817382 CTGACAGAAGAATCTCAATGACTGAGTCTTGGAGCAGGCTAACCATTAAGAGGCCGAGAAAATAA CTGACAGAAGAATCTCAATGACTGAGTCTTGGGGCAGGCTAACCATTAAGAGGCCGAGAAAATAA T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40817380..40817643 26863196 MeRIP-seq:(Medium) rs1447691221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581163,Human_RBP_ID_14500069,Human_RBP_ID_23949441 58862 RMVar_ID_58862 Human_SNP_ID_704365261 m1A Human chr22 - 40824846 40824837 40824847 GCAGACAGAAATGCATCTGTTACATAAATGAGAAAAAGCTATTATGCTGATGGAGCATGCTTTTT GCAGACAGAAATGCATCTGTTACATAAATGA__________TTATGCTGATGGAGCATGCTTTTT ATAGCTTTTTC A ST13 Ensembl:ENSG00000100380 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1283087283 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_125045,RMVar_hsa_circ_214506 58863 RMVar_ID_58863 Human_SNP_ID_704365804 m1A Human chr22 + 40827153 40827153 40827153 TCACTAAGAATTTCATTGAGTCCAGGCATTCCAGCCATTCCAGGCATGCCCCCTCCCATTCCAGG TCACTAAGAATTTCATTGAGTCCAGGCATTCCGGCCATTCCAGGCATGCCCCCTCCCATTCCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr22:40827103..40827178;chr22:40827076..40827175 26863196,32194978 MeRIP-seq:(Medium) rs757482172 Functional Loss SNV dbSNP153 33..33 33 - - - 58864 RMVar_ID_58864 Human_SNP_ID_704374202 m1A Human chr22 - 40856564 40856564 40856564 GCCTGGGCCTGGAACCGGGCCGTAGCCCCCCCAGTTTCGCCCACCACCTCCCTACCATGGACCCC GCCTGGGCCTGGAACCGGGCCGTAGCCCCCCCGGTTTCGCCCACCACCTCCCTACCATGGACCCC T C ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:40856501..40856625 26863196 MeRIP-seq:(Medium) rs1269730043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581216,Human_RBP_ID_4699846,Human_RBP_ID_14501059,Human_RBP_ID_24381839,Human_RBP_ID_27038607 58865 RMVar_ID_58865 Human_SNP_ID_704374219 m1A Human chr22 - 40856573 40856573 40856573 CGAGCCAGCGCCTGGGCCTGGAACCGGGCCGTAGCCCCCCCAGTTTCGCCCACCACCTCCCTACC CGAGCCAGCGCCTGGGCCTGGAACCGGGCCGTGGCCCCCCCAGTTTCGCCCACCACCTCCCTACC T C ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr22:40856521..40856624 26863410 MeRIP-seq:(Medium) rs982164548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581216,Human_RBP_ID_782314,Human_RBP_ID_4708678,Human_RBP_ID_17399855,Human_RBP_ID_24381839,Human_RBP_ID_27038607,Human_RBP_ID_27308728 58866 RMVar_ID_58866 Human_SNP_ID_704374230 m1A Human chr22 - 40856583 40856583 40856583 GCGGTCACGCCGAGCCAGCGCCTGGGCCTGGAACCGGGCCGTAGCCCCCCCAGTTTCGCCCACCA GCGGTCACGCCGAGCCAGCGCCTGGGCCTGGAGCCGGGCCGTAGCCCCCCCAGTTTCGCCCACCA T C ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:40856426..40856788;chr22:40856426..40856789 26863196 MeRIP-seq:(Medium) rs1391168837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581217,Human_RBP_ID_782314,Human_RBP_ID_4708678,Human_RBP_ID_17399855,Human_RBP_ID_22085486,Human_RBP_ID_22270858 58867 RMVar_ID_58867 Human_SNP_ID_704374252 m1A Human chr22 - 40856609 40856609 40856609 GTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCAGCGCCTGGGCCTGGAACCGGGC GTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCTCGCCGAGCCAGCGCCTGGGCCTGGAACCGGGC T A ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr22:40856426..40856675;chr22:40856533..40856632 26863196,26863410 MeRIP-seq:(Medium) rs1410123739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4699847,Human_RBP_ID_17399856,Human_RBP_ID_22270859,Human_RBP_ID_22454482 58868 RMVar_ID_58868 Human_SNP_ID_704374260 m1A Human chr22 + 40856620 40856617 40856620 GGCCCAGGCGCTGGCTCGGCGTGACCGCGCAGAAGGGGGCGGCTGCCGCAAGACAGAACAGACTA GGCCCAGGCGCTGGCTCGGCGTGACCGCGC___AGGGGGCGGCTGCCGCAAGACAGAACAGACTA CAGA C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:40856536..40856633 26863410 MeRIP-seq:(Medium) rs1479877123 Functional Loss DEL dbSNP153 31..33 33 - - - 58869 RMVar_ID_58869 Human_SNP_ID_704374276 m1A Human chr22 - 40856631 40856631 40856631 CGGGGAGGTTCTAGTCTGTTCTGTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCA CGGGGAGGTTCTAGTCTGTTCTGTCTTGCGGCGGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCA T C ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1209211684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4699849,Human_RBP_ID_22454482 58870 RMVar_ID_58870 Human_SNP_ID_704374590 m1A Human chr22 + 40857199 40857199 40857199 GTGAGTTAGGCCGTAATGCCTTGGCTGCTCTCAGCCCCCAAGCTGGTTCCCGCTGTAGCAAACGT GTGAGTTAGGCCGTAATGCCTTGGCTGCTCTCGGCCCCCAAGCTGGTTCCCGCTGTAGCAAACGT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:40857150..40857263 26863196 MeRIP-seq:(Medium) rs1335744952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581219,Human_RBP_ID_4708680 Human_Splice_Rec_2170113,Human_Splice_Rec_2170117,Human_Splice_Rec_2170121,Human_Splice_Rec_2170123,Human_Splice_Rec_2170143 58871 RMVar_ID_58871 Human_SNP_ID_704381175 m1A Human chr22 + 40882030 40882030 40882030 AGAGCCTCCCTGGCAAACAATTACCATCACACAAAGCCATACTTTTTGTGCCTCGGCGAGATCCC AGAGCCTCCCTGGCAAACAATTACCATCACACGAAGCCATACTTTTTGTGCCTCGGCGAGATCCC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:40881961..40882133 26863196 MeRIP-seq:(Medium) rs765710614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17286199,Human_RBP_ID_17399369,Human_RBP_ID_17986965,Human_RBP_ID_18329705,Human_RBP_ID_27494475 Human_miRNA_ID_258540,Human_miRNA_ID_262336,Human_miRNA_ID_2044055,Human_miRNA_ID_2046206 RMVar_hsa_circ_284435,RMVar_hsa_circ_310383,RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214515,RMVar_hsa_circ_214516,RMVar_hsa_circ_214514,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_273429,RMVar_hsa_circ_278374,RMVar_hsa_circ_126281,RMVar_hsa_circ_214520,RMVar_hsa_circ_214521,RMVar_hsa_circ_214519,RMVar_hsa_circ_214517 58872 RMVar_ID_58872 Human_SNP_ID_704399489 m1A Human chr22 - 40953506 40953503 40953507 AGGGAACAGTGCATTCTGCTTGTAACACACACACATACTCTTTAGGACCTCAGGCTGCAGCTGCA AGGGAACAGTGCATTCTGCTTGTAACACACA____TACTCTTTAGGACCTCAGGCTGCAGCTGCA ATGTG A L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:40953503..40953600 26863196 MeRIP-seq:(Medium) rs943575956 Functional Loss DEL dbSNP153 32..35 33 - - - 58873 RMVar_ID_58873 Human_SNP_ID_704401241 m1A Human chr22 + 40960329 40960328 40960329 AATTGATGTGTTAAGAGTGCCTGAAGGAGAGGAAAATGACTCAGGGTGGAAGAGTCAGGAAAAGC AATTGATGTGTTAAGAGTGCCTGAAGGAGAGG_AAATGACTCAGGGTGGAAGAGTCAGGAAAAGC GA G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40960319..40960538 26863196 MeRIP-seq:(Medium) rs1161594765 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14501818 RMVar_hsa_circ_83622,RMVar_hsa_circ_214517,RMVar_hsa_circ_214530,RMVar_hsa_circ_118698,RMVar_hsa_circ_214531,RMVar_hsa_circ_270699,RMVar_hsa_circ_275606,RMVar_hsa_circ_214532 58874 RMVar_ID_58874 Human_SNP_ID_704417470 m1A Human chr22 + 41022504 41022504 41022504 CTCTTTCTGATCTTTTTTATGGCCTAAACTCGAGATCTCCCCACCCTAGTGCCCCCACCCTGCCA CTCTTTCTGATCTTTTTTATGGCCTAAACTCGCGATCTCCCCACCCTAGTGCCCCCACCCTGCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41022453..41022599 26863196 MeRIP-seq:(Medium) rs1382287239 Functional Loss SNV dbSNP153 33..33 33 - - - 58875 RMVar_ID_58875 Human_SNP_ID_704435413 m1A Human chr22 + 41091812 41091810 41091812 CGCCATCTTGTTTGTGTGCTAGGCTGGGGGGGAGAGAGGGCGAGAGAGAGCGGGCGAGAGTGGGC CGCCATCTTGTTTGTGTGCTAGGCTGGGGGG__GAGAGGGCGAGAGAGAGCGGGCGAGAGTGGGC GGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41091726..41092001 26863196 MeRIP-seq:(Medium) rs920405484 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_66017,Human_RBP_ID_246637,Human_RBP_ID_3676142,Human_RBP_ID_4699958,Human_RBP_ID_5203894,Human_RBP_ID_5324210,Human_RBP_ID_5529957,Human_RBP_ID_8235605,Human_RBP_ID_8729640,Human_RBP_ID_9432901,Human_RBP_ID_17069245,Human_RBP_ID_17671126,Human_RBP_ID_18423653,Human_RBP_ID_18463979,Human_RBP_ID_22087392,Human_RBP_ID_22454708,Human_RBP_ID_22723961,Human_RBP_ID_24381288,Human_RBP_ID_24553780,Human_RBP_ID_26345468,Human_RBP_ID_26770989 58876 RMVar_ID_58876 Human_SNP_ID_704435418 m1A Human chr22 + 41091812 41091812 41091812 CGCCATCTTGTTTGTGTGCTAGGCTGGGGGGGAGAGAGGGCGAGAGAGAGCGGGCGAGAGTGGGC CGCCATCTTGTTTGTGTGCTAGGCTGGGGGGGGGAGAGGGCGAGAGAGAGCGGGCGAGAGTGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41091726..41092001 26863196 MeRIP-seq:(Medium) rs956677949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66017,Human_RBP_ID_246637,Human_RBP_ID_3676142,Human_RBP_ID_4699958,Human_RBP_ID_5203894,Human_RBP_ID_5324210,Human_RBP_ID_5529957,Human_RBP_ID_8235605,Human_RBP_ID_8729640,Human_RBP_ID_9432901,Human_RBP_ID_17069245,Human_RBP_ID_17671126,Human_RBP_ID_18423653,Human_RBP_ID_18463979,Human_RBP_ID_22087392,Human_RBP_ID_22454708,Human_RBP_ID_22723961,Human_RBP_ID_24381288,Human_RBP_ID_24553780,Human_RBP_ID_26345468,Human_RBP_ID_26770989 58877 RMVar_ID_58877 Human_SNP_ID_704463938 m1A Human chr22 + 41178179 41178179 41178179 CCCCAGCAGCAACCACAGCAGCAACTCCAGCCACCCATGGGAGGGATGAGCCCCCAGGCTCAGCA CCCCAGCAGCAACCACAGCAGCAACTCCAGCCCCCCATGGGAGGGATGAGCCCCCAGGCTCAGCA A C EP300 Ensembl:ENSG00000100393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41178128..41178312 26863196 MeRIP-seq:(Medium) rs776688239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65423,Human_RBP_ID_8551181,Human_RBP_ID_17286247,Human_RBP_ID_17660029,Human_RBP_ID_17702121 Human_miRNA_ID_2215016 RMVar_hsa_circ_267084,RMVar_hsa_circ_96540,RMVar_hsa_circ_214579 58878 RMVar_ID_58878 Human_SNP_ID_704463939 m1A Human chr22 + 41178179 41178179 41178179 CCCCAGCAGCAACCACAGCAGCAACTCCAGCCACCCATGGGAGGGATGAGCCCCCAGGCTCAGCA CCCCAGCAGCAACCACAGCAGCAACTCCAGCCGCCCATGGGAGGGATGAGCCCCCAGGCTCAGCA A G EP300 Ensembl:ENSG00000100393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41178128..41178312 26863196 MeRIP-seq:(Medium) rs776688239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65423,Human_RBP_ID_8551181,Human_RBP_ID_17286247,Human_RBP_ID_17660029,Human_RBP_ID_17702121 Human_miRNA_ID_2215016 RMVar_hsa_circ_267084,RMVar_hsa_circ_96540,RMVar_hsa_circ_214579 58879 RMVar_ID_58879 Human_SNP_ID_704464151 m1A Human chr22 - 41178631 41178601 41178631 GCCGTGGAGAAGGGACAGGCTGGGGAGAGCGCACTTGATTGGAGAGAGAATTAGGGATCTGCTGG GCCGTGGAGAAGGGACAGGCTGGGGAGAGCGC______________________________TGG AGCAGATCCCTAATTCTCTCTCCAATCAAGT A AL035658.1,EP300-AS1 Ensembl:ENSG00000232754,Ensembl:ENSG00000231993 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41178519..41178729 26863196 MeRIP-seq:(Medium) rs1182099002 Functional Loss DEL dbSNP153 33..62 33 - - - 58880 RMVar_ID_58880 Human_SNP_ID_704464164 m1A Human chr22 - 41178626 41178622 41178626 GGAGAAGGGACAGGCTGGGGAGAGCGCACTTGATTGGAGAGAGAATTAGGGATCTGCTGGCCTTG GGAGAAGGGACAGGCTGGGGAGAGCGCACTTG____GAGAGAGAATTAGGGATCTGCTGGCCTTG CCAAT C AL035658.1,EP300-AS1 Ensembl:ENSG00000232754,Ensembl:ENSG00000231993 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41178478..41178765 26863196 MeRIP-seq:(Medium) rs797045560 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5600096 Clinvar_Rec_193 58881 RMVar_ID_58881 Human_SNP_ID_704464170 m1A Human chr22 - 41178626 41178626 41178626 GGAGAAGGGACAGGCTGGGGAGAGCGCACTTGATTGGAGAGAGAATTAGGGATCTGCTGGCCTTG GGAGAAGGGACAGGCTGGGGAGAGCGCACTTGGTTGGAGAGAGAATTAGGGATCTGCTGGCCTTG T C AL035658.1,EP300-AS1 Ensembl:ENSG00000232754,Ensembl:ENSG00000231993 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41178478..41178765 26863196 MeRIP-seq:(Medium) rs1172668323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5600096 58882 RMVar_ID_58882 Human_SNP_ID_704464175 m1A Human chr22 - 41178631 41178631 41178631 GCCGTGGAGAAGGGACAGGCTGGGGAGAGCGCACTTGATTGGAGAGAGAATTAGGGATCTGCTGG GCCGTGGAGAAGGGACAGGCTGGGGAGAGCGCCCTTGATTGGAGAGAGAATTAGGGATCTGCTGG T G AL035658.1,EP300-AS1 Ensembl:ENSG00000232754,Ensembl:ENSG00000231993 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41178519..41178729 26863196 MeRIP-seq:(Medium) rs766271527 Functional Loss SNV dbSNP153 33..33 33 - - - 58883 RMVar_ID_58883 Human_SNP_ID_704469881 m1A Human chr22 - 41197421 41197421 41197421 CCTACCAGTGCCAGGACTGCCAGAGCGGGAGGAGCGCGGCGCGGGCCAGCCGGGACTGCTGGACA CCTACCAGTGCCAGGACTGCCAGAGCGGGAGGGGCGCGGCGCGGGCCAGCCGGGACTGCTGGACA T C EP300-AS1 Ensembl:ENSG00000231993 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41197273..41197459 26863196 MeRIP-seq:(Medium) rs893968056 Functional Loss SNV dbSNP153 33..33 33 - - - 58884 RMVar_ID_58884 Human_SNP_ID_704471958 m1A Human chr22 - 41205338 41205338 41205338 TTCTCCATGAGACCTCAGTTTCGCCAAGCGTCACCAGGTGCAGGAAGCCATATTGGCCTGCCCCG TTCTCCATGAGACCTCAGTTTCGCCAAGCGTCCCCAGGTGCAGGAAGCCATATTGGCCTGCCCCG T G L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:41205330..41205417 26863410 MeRIP-seq:(Medium) rs928063884 Functional Loss SNV dbSNP153 33..33 33 - - - 58885 RMVar_ID_58885 Human_SNP_ID_704471991 m1A Human chr22 + 41205381 41205381 41205381 GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTATTGAGGTGAGAAGGCGAGGACTTAGCGTGACT GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTGTTGAGGTGAGAAGGCGAGGACTTAGCGTGACT A G L3MBTL2 Ensembl:ENSG00000100395 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:41205342..41205444;chr22:41205340..41205452 26863196 MeRIP-seq:(Medium) rs3804097 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_246062,Human_RBP_ID_4708682,Human_RBP_ID_19113495 Human_Splice_Rec_2170337,Human_Splice_Rec_2170363,Human_Splice_Rec_2170371,Human_Splice_Rec_2170401,Human_Splice_Rec_2170405,Human_Splice_Rec_2170437,Human_Splice_Rec_2170465 RMVar_hsa_circ_107484,RMVar_hsa_circ_214598 58886 RMVar_ID_58886 Human_SNP_ID_704471992 m1A Human chr22 + 41205381 41205381 41205381 GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTATTGAGGTGAGAAGGCGAGGACTTAGCGTGACT GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTTTTGAGGTGAGAAGGCGAGGACTTAGCGTGACT A T L3MBTL2 Ensembl:ENSG00000100395 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:41205342..41205444;chr22:41205340..41205452 26863196 MeRIP-seq:(Medium) rs3804097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246062,Human_RBP_ID_4708682,Human_RBP_ID_19113495 Human_Splice_Rec_2170337,Human_Splice_Rec_2170363,Human_Splice_Rec_2170371,Human_Splice_Rec_2170401,Human_Splice_Rec_2170405,Human_Splice_Rec_2170437,Human_Splice_Rec_2170465 RMVar_hsa_circ_107484,RMVar_hsa_circ_214598 58887 RMVar_ID_58887 Human_SNP_ID_704473274 m1A Human chr22 - 41209935 41209935 41209935 TCCTCTCCATCCTCAGGGGACACTCTGAAGGCACCTGGCTCAGAACCACTGCCATCCAAGGAGCG TCCTCTCCATCCTCAGGGGACACTCTGAAGGCGCCTGGCTCAGAACCACTGCCATCCAAGGAGCG T C L3MBTL2-AS1 Ensembl:ENSG00000235513 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:41209896..41213888 32194978 MeRIP-seq:(Medium) rs1276333569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2170524,Human_Splice_Rec_2170530,Human_Splice_Rec_2170532,Human_Splice_Rec_2170536 58888 RMVar_ID_58888 Human_SNP_ID_704484087 m1A Human chr22 - 41246061 41246061 41246061 CATCCATACCACTGTGCTGACCGCTCAGCCTGAAGAGCAGAGAATGCCATGGGTGGGACTGTGGG CATCCATACCACTGTGCTGACCGCTCAGCCTGCAGAGCAGAGAATGCCATGGGTGGGACTGTGGG T G RANGAP1 Ensembl:ENSG00000100401 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41245960..41246111 26863410 MeRIP-seq:(Medium) rs1457182744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581409,Human_RBP_ID_1382826,Human_RBP_ID_1612549,Human_RBP_ID_8551252,Human_RBP_ID_14504316,Human_RBP_ID_23949933,Human_RBP_ID_26498859,Human_RBP_ID_27308890 Human_miRNA_ID_1768433 RMVar_hsa_circ_85248,RMVar_hsa_circ_109735,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_126495,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_214618,RMVar_hsa_circ_77274,RMVar_hsa_circ_214617,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607 58889 RMVar_ID_58889 Human_SNP_ID_704484144 m1A Human chr22 - 41246216 41246216 41246216 CCTGCCTTCCGGCCCGGCTCCCTGGCGGAGCCAGAACCCAGGGAGTTGCCCGCGTGCTGTCCTTC CCTGCCTTCCGGCCCGGCTCCCTGGCGGAGCCGGAACCCAGGGAGTTGCCCGCGTGCTGTCCTTC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41246168..41246490 26863196 MeRIP-seq:(Medium) rs1317427713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246068,Human_RBP_ID_4700354,Human_RBP_ID_26498863,Human_RBP_ID_27308894 Human_miRNA_ID_337279,Human_miRNA_ID_2084651 RMVar_hsa_circ_85248,RMVar_hsa_circ_109735,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_126495,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_214618,RMVar_hsa_circ_77274,RMVar_hsa_circ_214617,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607 58890 RMVar_ID_58890 Human_SNP_ID_704484190 m1A Human chr22 + 41246333 41246333 41246333 GTGGAGGTGAGTTTAATGGCGGAGCAGCTCACAGCCCTTTCCCCTGGGGGCCAACTCCCCACAAC GTGGAGGTGAGTTTAATGGCGGAGCAGCTCACGGCCCTTTCCCCTGGGGGCCAACTCCCCACAAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:41246301..41246375 26863196 MeRIP-seq:(Medium) rs1001991195 Functional Loss SNV dbSNP153 33..33 33 - - - 58891 RMVar_ID_58891 Human_SNP_ID_704484268 m1A Human chr22 - 41246610 41246609 41246611 CGCCCGCCACAGTCTGCTGCAGACGCTGTACAAGGTCTAGACTCAAAGCCTCTCCCATCCCTTGG CGCCCGCCACAGTCTGCTGCAGACGCTGTAC__GGTCTAGACTCAAAGCCTCTCCCATCCCTTGG CTT C RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41246509..41246610 26863410 MeRIP-seq:(Medium) rs1569165547 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1029587,Human_RBP_ID_1943598,Human_RBP_ID_14504321,Human_RBP_ID_18445557,Human_RBP_ID_23949950 Human_Splice_Rec_2170590,Human_Splice_Rec_2170620,Human_Splice_Rec_2170648 Human_miRNA_ID_2948095 RMVar_hsa_circ_85248,RMVar_hsa_circ_109735,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_126495,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_214618,RMVar_hsa_circ_77274,RMVar_hsa_circ_214617,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607 58892 RMVar_ID_58892 Human_SNP_ID_704484269 m1A Human chr22 - 41246610 41246610 41246610 CGCCCGCCACAGTCTGCTGCAGACGCTGTACAAGGTCTAGACTCAAAGCCTCTCCCATCCCTTGG CGCCCGCCACAGTCTGCTGCAGACGCTGTACATGGTCTAGACTCAAAGCCTCTCCCATCCCTTGG T A RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41246509..41246610 26863410 MeRIP-seq:(Medium) rs1363251863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029587,Human_RBP_ID_1943598,Human_RBP_ID_14504321,Human_RBP_ID_18445557,Human_RBP_ID_23949950 Human_Splice_Rec_2170590,Human_Splice_Rec_2170620,Human_Splice_Rec_2170648 Human_miRNA_ID_2948095 RMVar_hsa_circ_85248,RMVar_hsa_circ_109735,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_126495,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_214618,RMVar_hsa_circ_77274,RMVar_hsa_circ_214617,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607 58893 RMVar_ID_58893 Human_SNP_ID_704485251 m1A Human chr22 - 41249817 41249817 41249817 AGCAGCCTGCCCCTGCTGCTTCTGCCCTACAGATGCCCTGATGCAGAAGGCTTTCAACTCCTCGT AGCAGCCTGCCCCTGCTGCTTCTGCCCTACAGTTGCCCTGATGCAGAAGGCTTTCAACTCCTCGT T A RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41249776..41249825 32194978 MeRIP-seq:(Medium) rs1173523795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3963322,Human_RBP_ID_5389386,Human_RBP_ID_18790200,Human_RBP_ID_19113507,Human_RBP_ID_22550799,Human_RBP_ID_22674368 Human_Splice_Rec_2170586,Human_Splice_Rec_2170587,Human_Splice_Rec_2170616,Human_Splice_Rec_2170617,Human_Splice_Rec_2170644,Human_Splice_Rec_2170645 RMVar_hsa_circ_6949,RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_77274,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_269361,RMVar_hsa_circ_340150,RMVar_hsa_circ_331078,RMVar_hsa_circ_123915,RMVar_hsa_circ_214620,RMVar_hsa_circ_214621 58894 RMVar_ID_58894 Human_SNP_ID_704485418 m1A Human chr22 - 41250372 41250372 41250372 GAGGCGAGGGGGACGGTTCCTGGAAAAGATAGAAAGGGGTGGAAGGACATGTGGTGCCTCTTCCC GAGGCGAGGGGGACGGTTCCTGGAAAAGATAGGAAGGGGTGGAAGGACATGTGGTGCCTCTTCCC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41250219..41250497 26863196 MeRIP-seq:(Medium) rs1021323047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387423,Human_RBP_ID_26345474 RMVar_hsa_circ_6949,RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_77274,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_331078,RMVar_hsa_circ_123915,RMVar_hsa_circ_214620,RMVar_hsa_circ_214621 58895 RMVar_ID_58895 Human_SNP_ID_704486136 m1A Human chr22 + 41252949 41252949 41252949 CTTCTCTGGAGAGGGAAAAGCCAGGAAGGTGGAGACGTCTGCAGGAGGTGGGGAGGACAGCACGG CTTCTCTGGAGAGGGAAAAGCCAGGAAGGTGGCGACGTCTGCAGGAGGTGGGGAGGACAGCACGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:41252901..41253000 26863196 MeRIP-seq:(Medium) rs763423763 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 58896 RMVar_ID_58896 Human_SNP_ID_704486149 m1A Human chr22 - 41252990 41252984 41252991 TCTCCAGAGCCTCTGTGCCCCTACTTCCCAGGAGCCAGCTCCCGTGCTGTCCTCCCCACCTCCTG TCTCCAGAGCCTCTGTGCCCCTACTTCCCAG_______CTCCCGTGCTGTCCTCCCCACCTCCTG GCTGGCTC G RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41252953..41253038 26863196 MeRIP-seq:(Medium) rs1211385149 Functional Loss DEL dbSNP153 32..38 33 - - - Human_Splice_Rec_2170582,Human_Splice_Rec_2170612,Human_Splice_Rec_2170640 RMVar_hsa_circ_6949,RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_77274,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_123915,RMVar_hsa_circ_214621,RMVar_hsa_circ_103476,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_214624 58897 RMVar_ID_58897 Human_SNP_ID_704486152 m1A Human chr22 - 41252990 41252990 41252990 TCTCCAGAGCCTCTGTGCCCCTACTTCCCAGGAGCCAGCTCCCGTGCTGTCCTCCCCACCTCCTG TCTCCAGAGCCTCTGTGCCCCTACTTCCCAGGGGCCAGCTCCCGTGCTGTCCTCCCCACCTCCTG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41252953..41253038 26863196 MeRIP-seq:(Medium) rs201597542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2170582,Human_Splice_Rec_2170612,Human_Splice_Rec_2170640 RMVar_hsa_circ_6949,RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_77274,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_123915,RMVar_hsa_circ_214621,RMVar_hsa_circ_103476,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_214624 58898 RMVar_ID_58898 Human_SNP_ID_704486592 m1A Human chr22 - 41254444 41254444 41254444 GGAGGAGGAGGAAGGAGAAGAGGAAGAAGAGGAAGCAGAAGAAGAGGAGGAGGAAGATGAGGAAG GGAGGAGGAGGAAGGAGAAGAGGAAGAAGAGGGAGCAGAAGAAGAGGAGGAGGAAGATGAGGAAG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:41254351..41254559 26863196 MeRIP-seq:(Medium) rs1317532080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65438,Human_RBP_ID_209889,Human_RBP_ID_1614224,Human_RBP_ID_4700403,Human_RBP_ID_5203413,Human_RBP_ID_5653854,Human_RBP_ID_9392413,Human_RBP_ID_17069247,Human_RBP_ID_19008123,Human_RBP_ID_22675357,Human_RBP_ID_22821127,Human_RBP_ID_23015276,Human_RBP_ID_23119833,Human_RBP_ID_24547073,Human_RBP_ID_25683162,Human_RBP_ID_26345476,Human_RBP_ID_26498885 Human_Splice_Rec_2170580,Human_Splice_Rec_2170610,Human_Splice_Rec_2170638 RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_77274,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_123915,RMVar_hsa_circ_214621,RMVar_hsa_circ_30779,RMVar_hsa_circ_69833,RMVar_hsa_circ_103476,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_214624,RMVar_hsa_circ_346294,RMVar_hsa_circ_54496,RMVar_hsa_circ_214625 58899 RMVar_ID_58899 Human_SNP_ID_704487650 m1A Human chr22 + 41258023 41258023 41258023 TTCAGGTTGATGACCCGCAGCAGGGGGTTGACAGCGAAAGCCTGGGCCAGGGCAGTGATGCCAGG TTCAGGTTGATGACCCGCAGCAGGGGGTTGACGGCGAAAGCCTGGGCCAGGGCAGTGATGCCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr22:41257916..41258089;chr22:41258001..41258025 26863196 MeRIP-seq:(Medium) rs772736694 Functional Loss SNV dbSNP153 33..33 33 - - - 58900 RMVar_ID_58900 Human_SNP_ID_704487797 m1A Human chr22 - 41258530 41258528 41258530 TCCCTAGAGAAGGACGCCATGTCGAAGGGGTTATGTTGTGTAGGTGGGTGGGCTAGGAGGGCCCC TCCCTAGAGAAGGACGCCATGTCGAAGGGGTT__GTTGTGTAGGTGGGTGGGCTAGGAGGGCCCC CAT C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41258528..41258618 26863196 MeRIP-seq:(Medium) rs1413290031 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10053926 RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_82171,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_69833,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_346294,RMVar_hsa_circ_325141,RMVar_hsa_circ_214625,RMVar_hsa_circ_293949,RMVar_hsa_circ_81774,RMVar_hsa_circ_214627,RMVar_hsa_circ_214628,RMVar_hsa_circ_214631,RMVar_hsa_circ_320288 58901 RMVar_ID_58901 Human_SNP_ID_704487799 m1A Human chr22 - 41258530 41258530 41258530 TCCCTAGAGAAGGACGCCATGTCGAAGGGGTTATGTTGTGTAGGTGGGTGGGCTAGGAGGGCCCC TCCCTAGAGAAGGACGCCATGTCGAAGGGGTTGTGTTGTGTAGGTGGGTGGGCTAGGAGGGCCCC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41258528..41258618 26863196 MeRIP-seq:(Medium) rs1351638529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10053926 RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_82171,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_69833,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_346294,RMVar_hsa_circ_325141,RMVar_hsa_circ_214625,RMVar_hsa_circ_293949,RMVar_hsa_circ_81774,RMVar_hsa_circ_214627,RMVar_hsa_circ_214628,RMVar_hsa_circ_214631,RMVar_hsa_circ_320288 58902 RMVar_ID_58902 Human_SNP_ID_704490483 m1A Human chr22 - 41268140 41268140 41268140 CTTCTTTCCGTTGCAGCGCTGCCACTGGAGTGACATGTTCACGGGAAGGCTGCGGACCGAGATCC CTTCTTTCCGTTGCAGCGCTGCCACTGGAGTGGCATGTTCACGGGAAGGCTGCGGACCGAGATCC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41264836..41274633 32194978 MeRIP-seq:(Medium) rs755223961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929934,Human_RBP_ID_3962458,Human_RBP_ID_5149047,Human_RBP_ID_8864269,Human_RBP_ID_9392420,Human_RBP_ID_23015438,Human_RBP_ID_24547149,Human_RBP_ID_26345478 Human_Splice_Rec_2170566,Human_Splice_Rec_2170567,Human_Splice_Rec_2170596,Human_Splice_Rec_2170597,Human_Splice_Rec_2170624,Human_Splice_Rec_2170625,Human_Splice_Rec_2170650,Human_Splice_Rec_2170651,Human_Splice_Rec_2170666,Human_Splice_Rec_2170667,Human_Splice_Rec_2170674 Human_miRNA_ID_2996850 RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_82171,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_14277,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_346294,RMVar_hsa_circ_214625,RMVar_hsa_circ_293949,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_100108,RMVar_hsa_circ_335522,RMVar_hsa_circ_328022,RMVar_hsa_circ_312185,RMVar_hsa_circ_276668,RMVar_hsa_circ_214633,RMVar_hsa_circ_214634,RMVar_hsa_circ_274153,RMVar_hsa_circ_355825,RMVar_hsa_circ_104098,RMVar_hsa_circ_214635,RMVar_hsa_circ_214636 58903 RMVar_ID_58903 Human_SNP_ID_704491961 m1A Human chr22 - 41273137 41273137 41273137 AGAGACTGGGTTGAGTCTCCATTTATAAGTCAAGGGAACTGAGGCTCAGAGGGGCTCATTAAATA AGAGACTGGGTTGAGTCTCCATTTATAAGTCAGGGGAACTGAGGCTCAGAGGGGCTCATTAAATA T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41273134..41273225 26863196 MeRIP-seq:(Medium) rs571627380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14504688 RMVar_hsa_circ_85248,RMVar_hsa_circ_117905,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_14277,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_346294,RMVar_hsa_circ_214625,RMVar_hsa_circ_293949,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_100108,RMVar_hsa_circ_335522,RMVar_hsa_circ_312185,RMVar_hsa_circ_276668,RMVar_hsa_circ_214633,RMVar_hsa_circ_214634,RMVar_hsa_circ_274153,RMVar_hsa_circ_355825,RMVar_hsa_circ_104098,RMVar_hsa_circ_214635,RMVar_hsa_circ_214636 58904 RMVar_ID_58904 Human_SNP_ID_704494230 m1A Human chr22 - 41281077 41281077 41281077 TTCTTACTGCAACTTTGGCCTCCTCAGTCTGCAGATCTCCAGGGGAGCCCACCAGCCTAGTCAAC TTCTTACTGCAACTTTGGCCTCCTCAGTCTGCGGATCTCCAGGGGAGCCCACCAGCCTAGTCAAC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr22:41281051..41281100;chr22:41281026..41281100 26863196 MeRIP-seq:(Medium) rs911024488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65444,Human_RBP_ID_581439,Human_RBP_ID_932201,Human_RBP_ID_2720255,Human_RBP_ID_14504980,Human_RBP_ID_19113517,Human_RBP_ID_20768490,Human_RBP_ID_25674489 Human_Splice_Rec_2170562,Human_Splice_Rec_2170592,Human_Splice_Rec_2170662,Human_Splice_Rec_2170678 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214622,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_340150,RMVar_hsa_circ_214623,RMVar_hsa_circ_316489,RMVar_hsa_circ_346294,RMVar_hsa_circ_214625,RMVar_hsa_circ_293949,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_335522,RMVar_hsa_circ_276668,RMVar_hsa_circ_214633,RMVar_hsa_circ_274153,RMVar_hsa_circ_355825,RMVar_hsa_circ_104098,RMVar_hsa_circ_214635,RMVar_hsa_circ_214636,RMVar_hsa_circ_273308,RMVar_hsa_circ_214637 58905 RMVar_ID_58905 Human_SNP_ID_704495364 m1A Human chr22 - 41285074 41285074 41285074 CCGCTGAACTGCAGCGTCGGCTTCCTGGGCTCAAGCGATCCTCCCACCTCAACCTCCCAAGTCAT CCGCTGAACTGCAGCGTCGGCTTCCTGGGCTCTAGCGATCCTCCCACCTCAACCTCCCAAGTCAT T A RANGAP1 Ensembl:ENSG00000100401 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41285072..41285381 32194978 MeRIP-seq:(Medium) rs1308504642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1612635,Human_RBP_ID_5424564,Human_RBP_ID_5504912,Human_RBP_ID_7086677,Human_RBP_ID_14505211,Human_RBP_ID_18790282 Human_Splice_Rec_2170560,Human_Splice_Rec_2170676 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 58906 RMVar_ID_58906 Human_SNP_ID_704495704 m1A Human chr22 - 41286101 41286101 41286101 AGAGCTAACAGACTAGCCGGCTGGACATCTGGACCGCTGGATCCGGAGGTGGCGACCCCGGCCTG AGAGCTAACAGACTAGCCGGCTGGACATCTGGGCCGCTGGATCCGGAGGTGGCGACCCCGGCCTG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41286001..41286200 26863410 MeRIP-seq:(Medium) rs940508899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781442,Human_RBP_ID_1612647,Human_RBP_ID_1943655,Human_RBP_ID_3673947,Human_RBP_ID_4708683,Human_RBP_ID_7086698,Human_RBP_ID_8551332,Human_RBP_ID_8864272,Human_RBP_ID_9332877,Human_RBP_ID_14505270,Human_RBP_ID_18790291,Human_RBP_ID_23015277,Human_RBP_ID_23119871,Human_RBP_ID_27565413 Human_miRNA_ID_1983584,Human_miRNA_ID_2017450,Human_miRNA_ID_2899459 RMVar_hsa_circ_85248,RMVar_hsa_circ_214606,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 58907 RMVar_ID_58907 Human_SNP_ID_704495714 m1A Human chr22 - 41286135 41286135 41286135 TGGTGCTGGAAGCGCGTGAGGCCGGGAGCTCGAGAGAGCTAACAGACTAGCCGGCTGGACATCTG TGGTGCTGGAAGCGCGTGAGGCCGGGAGCTCGGGAGAGCTAACAGACTAGCCGGCTGGACATCTG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1320544910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833750,Human_RBP_ID_1612648,Human_RBP_ID_4700482,Human_RBP_ID_9332877,Human_RBP_ID_9392422,Human_RBP_ID_14505271,Human_RBP_ID_18423654,Human_RBP_ID_18790293,Human_RBP_ID_23014014 Human_miRNA_ID_2791138 RMVar_hsa_circ_85248,RMVar_hsa_circ_214606,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 58908 RMVar_ID_58908 Human_SNP_ID_704500375 m1A Human chr22 + 41301639 41301639 41301639 GACGGAGCTGCCGGGGCGGCGGCGCCGGGAGCAGGATGCGGCCGCCCGTAATTAAATAGCATTTA GACGGAGCTGCCGGGGCGGCGGCGCCGGGAGCGGGATGCGGCCGCCCGTAATTAAATAGCATTTA A G ZC3H7B Ensembl:ENSG00000100403 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41301541..41301821 26863196 MeRIP-seq:(Medium) rs1439974555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781444,Human_RBP_ID_4708265,Human_RBP_ID_9127023 RMVar_hsa_circ_101564,RMVar_hsa_circ_268550,RMVar_hsa_circ_214638 58909 RMVar_ID_58909 Human_SNP_ID_704513629 m1A Human chr22 - 41351622 41351622 41351622 GGCCTTACCATGCTGCTGCTGGCCTTCCCCGCATGCGCCTCCATCTGCTGCCAGTACTTCTTAGA GGCCTTACCATGCTGCTGCTGGCCTTCCCCGCGTGCGCCTCCATCTGCTGCCAGTACTTCTTAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41351572..41355545 32194978 MeRIP-seq:(Medium) rs1051158148 Functional Loss SNV dbSNP153 33..33 33 - - - 58910 RMVar_ID_58910 Human_SNP_ID_704515191 m1A Human chr22 - 41357313 41357313 41357313 GTTGTATTTGCCAAAGTCGTCGTCCCGTGGGCACAGCAGCATGTCCTTGCGAGCCTTGGCCAACT GTTGTATTTGCCAAAGTCGTCGTCCCGTGGGCGCAGCAGCATGTCCTTGCGAGCCTTGGCCAACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41357265..41357429 26863196 MeRIP-seq:(Medium) rs776667239 Functional Loss SNV dbSNP153 33..33 33 - - - 58911 RMVar_ID_58911 Human_SNP_ID_704515537 m1A Human chr22 - 41358452 41358452 41358452 GATCCTGAGCTCATGGTGTCCTGCCCTCTGCCACCTTTCCCAGAGCGCATGTCAGGAGGTGACCT GATCCTGAGCTCATGGTGTCCTGCCCTCTGCCGCCTTTCCCAGAGCGCATGTCAGGAGGTGACCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41358404..41358785 26863196 MeRIP-seq:(Medium) rs556611607 Functional Loss SNV dbSNP153 33..33 33 - - - 58912 RMVar_ID_58912 Human_SNP_ID_704515554 m1A Human chr22 + 41358542 41358542 41358542 GGTGAGGGTCTGGGGGAATGCGGAGAAAAGGGAGGCTTGACCCCGGGCACCATGGGCCACTCCAG GGTGAGGGTCTGGGGGAATGCGGAGAAAAGGGTGGCTTGACCCCGGGCACCATGGGCCACTCCAG A T ZC3H7B Ensembl:ENSG00000100403 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41358391..41358763 26863196 MeRIP-seq:(Medium) rs1055469261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246644,Human_RBP_ID_5530127,Human_RBP_ID_8207358,Human_RBP_ID_8235516,Human_RBP_ID_8865999,Human_RBP_ID_9433229,Human_RBP_ID_18790317,Human_RBP_ID_22087203,Human_RBP_ID_26500377 Human_miRNA_ID_544928,Human_miRNA_ID_580163,Human_miRNA_ID_940486 58913 RMVar_ID_58913 Human_SNP_ID_704515602 m1A Human chr22 + 41358711 41358711 41358711 CTCCCAGCTGTCTGGGACTTCAGTGGACCCCCAGCCCCTGCCCCCACTCACCAAGGCCTCGCTCG CTCCCAGCTGTCTGGGACTTCAGTGGACCCCCCGCCCCTGCCCCCACTCACCAAGGCCTCGCTCG A C ZC3H7B Ensembl:ENSG00000100403 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:41358701..41358775 26863196 MeRIP-seq:(Medium) rs1390661979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581463,Human_RBP_ID_4708266,Human_RBP_ID_18194150 Human_miRNA_ID_1359514 58914 RMVar_ID_58914 Human_SNP_ID_704515603 m1A Human chr22 + 41358711 41358711 41358711 CTCCCAGCTGTCTGGGACTTCAGTGGACCCCCAGCCCCTGCCCCCACTCACCAAGGCCTCGCTCG CTCCCAGCTGTCTGGGACTTCAGTGGACCCCCTGCCCCTGCCCCCACTCACCAAGGCCTCGCTCG A T ZC3H7B Ensembl:ENSG00000100403 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:41358701..41358775 26863196 MeRIP-seq:(Medium) rs1390661979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581463,Human_RBP_ID_4708266,Human_RBP_ID_18194150 Human_miRNA_ID_1359514 58915 RMVar_ID_58915 Human_SNP_ID_704515617 m1A Human chr22 - 41358750 41358750 41358750 GAGGAGGGGGGTGCACACAGACATGTCAGACGAGAGGGACGAGCGAGGCCTTGGTGAGTGGGGGC GAGGAGGGGGGTGCACACAGACATGTCAGACGGGAGGGACGAGCGAGGCCTTGGTGAGTGGGGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:41358700..41358900 32194978 MeRIP-seq:(Medium) rs1008518451 Functional Loss SNV dbSNP153 33..33 33 - - - 58916 RMVar_ID_58916 Human_SNP_ID_704515810 m1A Human chr22 + 41359495 41359495 41359495 CCATGGCTCAGAGGTGATTCGGGCAGCCAGGGACAGGAGCCACCCTCCCCAGGCCCAACTCTGCT CCATGGCTCAGAGGTGATTCGGGCAGCCAGGGTCAGGAGCCACCCTCCCCAGGCCCAACTCTGCT A T ZC3H7B Ensembl:ENSG00000100403 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:41359445..41359561 26863196 MeRIP-seq:(Medium) rs1435135065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581471,Human_RBP_ID_5204749,Human_RBP_ID_5529973,Human_RBP_ID_7086794,Human_RBP_ID_18463982,Human_RBP_ID_26500382 58917 RMVar_ID_58917 Human_SNP_ID_704515875 m1A Human chr22 + 41359744 41359744 41359744 CCACAGGGTAAGGAAGAGAGAGTGGGAGGCAGAGTGTGATGGGGAGGAGGGACAGGAAGACCCTT CCACAGGGTAAGGAAGAGAGAGTGGGAGGCAGGGTGTGATGGGGAGGAGGGACAGGAAGACCCTT A G ZC3H7B Ensembl:ENSG00000100403 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41359704..41359855 26863196 MeRIP-seq:(Medium) rs965205827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529974,Human_RBP_ID_7086798,Human_RBP_ID_8208667,Human_RBP_ID_24553784,Human_RBP_ID_26500385 58918 RMVar_ID_58918 Human_SNP_ID_704522620 m1A Human chr22 + 41382088 41382088 41382088 GGGCGGCGGAAAGAAGCCGCCTGTGGACCCGCAGGCAGGACCCGGTCCGGGGCCGGGGCGCGCAG GGGCGGCGGAAAGAAGCCGCCTGTGGACCCGCGGGCAGGACCCGGTCCGGGGCCGGGGCGCGCAG A G TEF Ensembl:ENSG00000167074 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41382022..41382114 26863196 MeRIP-seq:(Medium) rs1458842710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80494,RMVar_hsa_circ_214660 58919 RMVar_ID_58919 Human_SNP_ID_704546824 m1A Human chr22 - 41468657 41468657 41468657 TCCCGAAGCTTCCGGTGGCCGGCTTAGTTAGGAGCTATGGCTAAACATCATCCTGATTTGATCTT TCCCGAAGCTTCCGGTGGCCGGCTTAGTTAGGGGCTATGGCTAAACATCATCCTGATTTGATCTT T C PHF5A Ensembl:ENSG00000100410 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:41468543..41468675;chr22:41468540..41468675 26863196 MeRIP-seq:(Medium) rs1183904756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029637,Human_RBP_ID_1612695,Human_RBP_ID_4708690,Human_RBP_ID_7087038,Human_RBP_ID_23950119 Human_Splice_Rec_2170755,Human_Splice_Rec_2170761 RMVar_hsa_circ_98699,RMVar_hsa_circ_214664 58920 RMVar_ID_58920 Human_SNP_ID_704546826 m1A Human chr22 - 41468660 41468660 41468660 AGTTCCCGAAGCTTCCGGTGGCCGGCTTAGTTAGGAGCTATGGCTAAACATCATCCTGATTTGAT AGTTCCCGAAGCTTCCGGTGGCCGGCTTAGTTTGGAGCTATGGCTAAACATCATCCTGATTTGAT T A PHF5A Ensembl:ENSG00000100410 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:41468560..41468668;chr22:41468546..41468700 26863196 MeRIP-seq:(Medium) rs776172063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1612695,Human_RBP_ID_4708690,Human_RBP_ID_7087038,Human_RBP_ID_23950119,Human_RBP_ID_27309065 Human_Splice_Rec_2170755,Human_Splice_Rec_2170761 RMVar_hsa_circ_98699,RMVar_hsa_circ_214664 58921 RMVar_ID_58921 Human_SNP_ID_704546827 m1A Human chr22 - 41468660 41468660 41468660 AGTTCCCGAAGCTTCCGGTGGCCGGCTTAGTTAGGAGCTATGGCTAAACATCATCCTGATTTGAT AGTTCCCGAAGCTTCCGGTGGCCGGCTTAGTTGGGAGCTATGGCTAAACATCATCCTGATTTGAT T C PHF5A Ensembl:ENSG00000100410 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:41468560..41468668;chr22:41468546..41468700 26863196 MeRIP-seq:(Medium) rs776172063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1612695,Human_RBP_ID_4708690,Human_RBP_ID_7087038,Human_RBP_ID_23950119,Human_RBP_ID_27309065 Human_Splice_Rec_2170755,Human_Splice_Rec_2170761 RMVar_hsa_circ_98699,RMVar_hsa_circ_214664 58922 RMVar_ID_58922 Human_SNP_ID_704548237 m1A Human chr22 - 41473887 41473887 41473887 CAGCCTCTTGTTCAGACCTTTCGCTCCTCAGGACACTGTAGCAACACTGGCCTTAGCTCTTATCC CAGCCTCTTGTTCAGACCTTTCGCTCCTCAGGGCACTGTAGCAACACTGGCCTTAGCTCTTATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41473884..41474247 26863196 MeRIP-seq:(Medium) rs1339388532 Functional Loss SNV dbSNP153 33..33 33 - - - 58923 RMVar_ID_58923 Human_SNP_ID_704550787 m1A Human chr22 + 41483957 41483957 41483957 TTAGACCTTATGGGGAAGGAGACAGAGGCTCCAGGAGATGACGAGGCTGGTGGATCTCCTGACGC TTAGACCTTATGGGGAAGGAGACAGAGGCTCCGGGAGATGACGAGGCTGGTGGATCTCCTGACGC A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41483947..41484030 26863196 MeRIP-seq:(Medium) rs1397630490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7087074 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666 58924 RMVar_ID_58924 Human_SNP_ID_704561142 m1A Human chr22 + 41524922 41524920 41524923 AGAGACCGACTACCTGACGGGCACGGATGGCAAGAAGTTCAGGCTGGAGGCTCCGGATGCAGATG AGAGACCGACTACCTGACGGGCACGGATGGC___AAGTTCAGGCTGGAGGCTCCGGATGCAGATG CAAG C ACO2 Ensembl:ENSG00000100412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41524816..41524996 26863196 MeRIP-seq:(Medium) rs750451539 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5203053,Human_RBP_ID_8866007,Human_RBP_ID_9300427,Human_RBP_ID_17987300,Human_RBP_ID_22454489 Human_Splice_Rec_2170796,Human_Splice_Rec_2170797,Human_Splice_Rec_2170830,Human_Splice_Rec_2170831 Human_miRNA_ID_2975338,Human_miRNA_ID_3008533,Human_miRNA_ID_3034276 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_214672,RMVar_hsa_circ_83338,RMVar_hsa_circ_93427,RMVar_hsa_circ_214675,RMVar_hsa_circ_82468,RMVar_hsa_circ_214683,RMVar_hsa_circ_321627 58925 RMVar_ID_58925 Human_SNP_ID_704561263 m1A Human chr22 + 41525241 41525241 41525241 AGGACACCTACCAGCACCCACCCAAGGACAGCAGCGGGCAGCATGTGGACGTGAGCCCCACCAGC AGGACACCTACCAGCACCCACCCAAGGACAGCTGCGGGCAGCATGTGGACGTGAGCCCCACCAGC A T ACO2 Ensembl:ENSG00000100412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41525156..41525279 26863196 MeRIP-seq:(Medium) rs1208628375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18194393,Human_RBP_ID_18471503,Human_RBP_ID_22454490,Human_RBP_ID_22768322,Human_RBP_ID_27821368 Human_Splice_Rec_2170798,Human_Splice_Rec_2170832 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_321627 58926 RMVar_ID_58926 Human_SNP_ID_704561579 m1A Human chr22 - 41526184 41526181 41526185 AGGGGTGGATGACAAGCCCTCCAGAGGCAGGCAGCAGGCCCCGGGGCCCAGGAGGGGTGACAGAG AGGGGTGGATGACAAGCCCTCCAGAGGCAGG____AGGCCCCGGGGCCCAGGAGGGGTGACAGAG TGCTG T POLR3H Ensembl:ENSG00000100413 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41526175..41526272 26863196 MeRIP-seq:(Medium) rs771415318 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_26501196 RMVar_hsa_circ_214684,RMVar_hsa_circ_84127 58927 RMVar_ID_58927 Human_SNP_ID_704561626 m1A Human chr22 + 41526314 41526314 41526314 TGACCACATCTCAGCTGCTGGCCCCTGGCTCAAGTTCCGTGGGCACTTGGATAACATCTCCAACA TGACCACATCTCAGCTGCTGGCCCCTGGCTCATGTTCCGTGGGCACTTGGATAACATCTCCAACA A T POLR3H Ensembl:ENSG00000100413 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs764260085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214684,RMVar_hsa_circ_84127 58928 RMVar_ID_58928 Human_SNP_ID_704562030 m1A Human chr22 - 41527377 41527377 41527377 GCAAAGCTCTTGGTGATGATGGCCCGGCCCCCAAGGTGGCGAGGCTCCAGAGCTGCATGCTCCCG GCAAAGCTCTTGGTGATGATGGCCCGGCCCCCGAGGTGGCGAGGCTCCAGAGCTGCATGCTCCCG T C POLR3H Ensembl:ENSG00000100413 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41527301..41527402 32194978 MeRIP-seq:(Medium) rs1404085379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27039043,Human_RBP_ID_27309111 RMVar_hsa_circ_214684,RMVar_hsa_circ_84127 58929 RMVar_ID_58929 Human_SNP_ID_704562274 m1A Human chr22 - 41528056 41528053 41528056 GTGCAGGAGGGGAAACAAGGTGGCTGCCCCTCACCCCACCACCTCAGGGGGACCCGGGCCCCTAA GTGCAGGAGGGGAAACAAGGTGGCTGCCCCTC___CCACCACCTCAGGGGGACCCGGGCCCCTAA GGGT G POLR3H Ensembl:ENSG00000100413 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41528051..41528201 32194978 MeRIP-seq:(Medium) rs1569026590 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3676785,Human_RBP_ID_4708273,Human_RBP_ID_17987319 Human_miRNA_ID_1704708,Human_miRNA_ID_2391487,Human_miRNA_ID_2391488,Human_miRNA_ID_2592728,Human_miRNA_ID_2592729 RMVar_hsa_circ_214684,RMVar_hsa_circ_84127,RMVar_hsa_circ_214685,RMVar_hsa_circ_377486 58930 RMVar_ID_58930 Human_SNP_ID_704562470 m1A Human chr22 + 41528613 41528613 41528613 GCCCTCAACAGAATGAAGGAACTGCAACAGTGAGGGCAGTGCCTCCCCGCCCCGCCGCTGGCGTC GCCCTCAACAGAATGAAGGAACTGCAACAGTGGGGGCAGTGCCTCCCCGCCCCGCCGCTGGCGTC A G ACO2 Ensembl:ENSG00000100412 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41528565..41528792 26863196 MeRIP-seq:(Medium) rs1569027545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581563,Human_RBP_ID_22454492 Human_miRNA_ID_2389082,Human_miRNA_ID_2476983,Human_miRNA_ID_2962767,Human_miRNA_ID_3022751 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667 58931 RMVar_ID_58931 Human_SNP_ID_704562630 m1A Human chr22 + 41529100 41529100 41529100 ACAGCCACAGCCACAGATGGATCCATCACTGCAGTGAAGGAGGAGCAGGGCCTAGATGGTGGAGG ACAGCCACAGCCACAGATGGATCCATCACTGCCGTGAAGGAGGAGCAGGGCCTAGATGGTGGAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41529050..41529150 32194978 MeRIP-seq:(Medium) rs1340862225 Functional Loss SNV dbSNP153 33..33 33 - - - 58932 RMVar_ID_58932 Human_SNP_ID_704563267 m1A Human chr22 + 41530800 41530800 41530800 CGTGTCAACAAAGCTCTCGTCCACCACCCGGAAGCGGATCTCCTCGCCGGTGTCCATGTAGAGGT CGTGTCAACAAAGCTCTCGTCCACCACCCGGAGGCGGATCTCCTCGCCGGTGTCCATGTAGAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41530749..41530845 26863196 MeRIP-seq:(Medium) rs773692726 Functional Loss SNV dbSNP153 33..33 33 - - - 58933 RMVar_ID_58933 Human_SNP_ID_704566257 m1A Human chr22 - 41541773 41541773 41541773 GGATGGCTTCTGGTTACTTTGTGAGGTTGAAGATGAGGGTCTGTTGGGGGATGGAGGTGTGGACC GGATGGCTTCTGGTTACTTTGTGAGGTTGAAGGTGAGGGTCTGTTGGGGGATGGAGGTGTGGACC T C POLR3H Ensembl:ENSG00000100413 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41541768..41542000 26863196 MeRIP-seq:(Medium) rs969189434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214685,RMVar_hsa_circ_377486,RMVar_hsa_circ_329140,RMVar_hsa_circ_214690 58934 RMVar_ID_58934 Human_SNP_ID_704566279 m1A Human chr22 - 41541882 41541882 41541882 AGAAAGAGGATGCTTAGCTGGCTTTACGCATGAGACAGGTCCCTTCAGAAGAGGTGAGGTTGATT AGAAAGAGGATGCTTAGCTGGCTTTACGCATGCGACAGGTCCCTTCAGAAGAGGTGAGGTTGATT T G POLR3H Ensembl:ENSG00000100413 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41541880..41541978 26863196 MeRIP-seq:(Medium) rs952622783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214685,RMVar_hsa_circ_377486,RMVar_hsa_circ_329140,RMVar_hsa_circ_214690 58935 RMVar_ID_58935 Human_SNP_ID_704566429 m1A Human chr22 - 41542424 41542424 41542424 GGGGGCTGGGTGGAGAGAAGAGCCCTGAAGGCAGGAACTGGCATGTGCAAAGGCCCTGTGAAGAA GGGGGCTGGGTGGAGAGAAGAGCCCTGAAGGCCGGAACTGGCATGTGCAAAGGCCCTGTGAAGAA T G POLR3H Ensembl:ENSG00000100413 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41542422..41542655 26863196 MeRIP-seq:(Medium) rs1348862330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246107,Human_RBP_ID_17069249 RMVar_hsa_circ_214685,RMVar_hsa_circ_377486,RMVar_hsa_circ_329140,RMVar_hsa_circ_214690 58936 RMVar_ID_58936 Human_SNP_ID_704567044 m1A Human chr22 + 41544370 41544350 41544370 CGCCGCGAGACCCCGCCACGCCACGCCACTCCACGCCACGCCACTCCACGCCCCGCACCCGCGCC CGCCGCGAGACCC____________________CGCCACGCCACTCCACGCCCCGCACCCGCGCC CCGCCACGCCACGCCACTCCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41544046..41544475 26863196 MeRIP-seq:(Medium) rs1262133331 Functional Loss DEL dbSNP153 14..33 33 - - - 58937 RMVar_ID_58937 Human_SNP_ID_704567079 m1A Human chr22 + 41544380 41544380 41544380 CCCCGCCACGCCACGCCACTCCACGCCACGCCACTCCACGCCCCGCACCCGCGCCACGTGCCGCC CCCCGCCACGCCACGCCACTCCACGCCACGCCCCTCCACGCCCCGCACCCGCGCCACGTGCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:41544226..41544464;chr22:41544076..41544475;chr22:41544184..41544461 26863196 MeRIP-seq:(Medium) rs913530075 Functional Loss SNV dbSNP153 33..33 33 - - - 58938 RMVar_ID_58938 Human_SNP_ID_704567080 m1A Human chr22 + 41544380 41544380 41544380 CCCCGCCACGCCACGCCACTCCACGCCACGCCACTCCACGCCCCGCACCCGCGCCACGTGCCGCC CCCCGCCACGCCACGCCACTCCACGCCACGCCTCTCCACGCCCCGCACCCGCGCCACGTGCCGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:41544226..41544464;chr22:41544076..41544475;chr22:41544184..41544461 26863196 MeRIP-seq:(Medium) rs913530075 Functional Loss SNV dbSNP153 33..33 33 - - - 58939 RMVar_ID_58939 Human_SNP_ID_704578415 m1A Human chr22 - 41586191 41586191 41586191 GAATGCTATGCTTCCCCTCTCCCCCCATAGAAAATTGACCCTGAGGTGGCCGCCTTCCTGCAGAA GAATGCTATGCTTCCCCTCTCCCCCCATAGAAGATTGACCCTGAGGTGGCCGCCTTCCTGCAGAA T C PMM1 Ensembl:ENSG00000100417 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41586140..41586248 26863196 MeRIP-seq:(Medium) rs375494696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709113,Human_RBP_ID_19008143 Human_Splice_Rec_2170954,Human_Splice_Rec_2170982,Human_Splice_Rec_2170994,Human_Splice_Rec_2171008,Human_Splice_Rec_2171016,Human_Splice_Rec_2171022,Human_Splice_Rec_2171030 RMVar_hsa_circ_17915,RMVar_hsa_circ_309282 58940 RMVar_ID_58940 Human_SNP_ID_704587716 m1A Human chr22 - 41621027 41621027 41621027 GGGCCCTCCCTGTCCCCTCTCTGTCACCTCACAGTAGTCGTTGCCGGTAGCGGGTGTGGGGGCGC GGGCCCTCCCTGTCCCCTCTCTGTCACCTCACCGTAGTCGTTGCCGGTAGCGGGTGTGGGGGCGC T G DESI1 Ensembl:ENSG00000100418 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:41620926..41621050 26863410 MeRIP-seq:(Medium) rs1372273694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423656 RMVar_hsa_circ_108119,RMVar_hsa_circ_214698 58941 RMVar_ID_58941 Human_SNP_ID_704588138 m1A Human chr22 - 41621980 41621980 41621980 CCTGACATGTTGGCTACTGCTCACTAGGCGAAAGACGTTAACGTCAGTAACAGGCAAATTTAAAT CCTGACATGTTGGCTACTGCTCACTAGGCGAAGGACGTTAACGTCAGTAACAGGCAAATTTAAAT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:41621976..41622050 26863196 MeRIP-seq:(Medium) rs760110269 Functional Loss SNV dbSNP153 33..33 33 - - - 58942 RMVar_ID_58942 Human_SNP_ID_704590169 m1A Human chr22 - 41628065 41628065 41628065 GAAAATGTTTGTCCTTGTTTTCGTATTTGTTTACCATATAAGATAAATAAAGGCCATAAAGGAAA GAAAATGTTTGTCCTTGTTTTCGTATTTGTTTGCCATATAAGATAAATAAAGGCCATAAAGGAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41628061..41628219 26863196 MeRIP-seq:(Medium) rs1014488335 Functional Loss SNV dbSNP153 33..33 33 - - - 58943 RMVar_ID_58943 Human_SNP_ID_704599197 m1A Human chr22 - 41658352 41658352 41658352 ATGAAAAGAACTACTCTATTCAACCTCCTTACATGTCAGGTCCACTGCTTGTTCCGGCTCCATCA ATGAAAAGAACTACTCTATTCAACCTCCTTACGTGTCAGGTCCACTGCTTGTTCCGGCTCCATCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41658319..41658410 26863196 MeRIP-seq:(Medium) rs1435645584 Functional Loss SNV dbSNP153 33..33 33 - - - 58944 RMVar_ID_58944 Human_SNP_ID_704600602 m1A Human chr22 - 41663841 41663841 41663841 GACAAGGCCAGGCAGCCTGGCCACACTGCGGAAGGGCAGCTGGACGCGCGGCCTCTGGTCAGTCC GACAAGGCCAGGCAGCCTGGCCACACTGCGGAGGGGCAGCTGGACGCGCGGCCTCTGGTCAGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41663751..41663900 32194978 MeRIP-seq:(Medium) rs761339453 Functional Loss SNV dbSNP153 33..33 33 - - - 58945 RMVar_ID_58945 Human_SNP_ID_704603619 m1A Human chr22 - 41674219 41674219 41674219 GGGCAGTTGACCTGGGTCTTGAAAGAGTCGGGAGTGACAAGCTCAGAGAGCATGAACTGATGCTG GGGCAGTTGACCTGGGTCTTGAAAGAGTCGGGCGTGACAAGCTCAGAGAGCATGAACTGATGCTG T G SNU13 Ensembl:ENSG00000100138 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41674169..41674275 26863196 MeRIP-seq:(Medium) rs1039764891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581677,Human_RBP_ID_1943837,Human_RBP_ID_8207989,Human_RBP_ID_14509260,Human_RBP_ID_23950319 RMVar_hsa_circ_85280,RMVar_hsa_circ_121890,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_214713,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 58946 RMVar_ID_58946 Human_SNP_ID_704603634 m1A Human chr22 - 41674272 41674272 41674272 ACCAAAGAGATGTGCTGCAGGACTCCGGAGGCAGCCTGGGTGGGTGAGCCATGGGGCAGTTGACC ACCAAAGAGATGTGCTGCAGGACTCCGGAGGCGGCCTGGGTGGGTGAGCCATGGGGCAGTTGACC T C SNU13 Ensembl:ENSG00000100138 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581677,Human_RBP_ID_5119803,Human_RBP_ID_7087535,Human_RBP_ID_8207989,Human_RBP_ID_14509263,Human_RBP_ID_17987404,Human_RBP_ID_23950320 GWAS_ID_6864 RMVar_hsa_circ_85280,RMVar_hsa_circ_121890,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_214713,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 58947 RMVar_ID_58947 Human_SNP_ID_704603832 m1A Human chr22 + 41675026 41675026 41675026 CCTTCTTTGATGGTGACAGAACAGGCGATGACAGGCCTGGAGACCCCACAGGCTCTCCCCAGGGC CCTTCTTTGATGGTGACAGAACAGGCGATGACGGGCCTGGAGACCCCACAGGCTCTCCCCAGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41674901..41675075 32194978 MeRIP-seq:(Medium) rs141373614 Functional Loss SNV dbSNP153 33..33 33 - - - 58948 RMVar_ID_58948 Human_SNP_ID_704603836 m1A Human chr22 + 41675036 41675036 41675036 TGGTGACAGAACAGGCGATGACAGGCCTGGAGACCCCACAGGCTCTCCCCAGGGCCTGCTTGGAG TGGTGACAGAACAGGCGATGACAGGCCTGGAGCCCCCACAGGCTCTCCCCAGGGCCTGCTTGGAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:41674822..41681278 32194978 MeRIP-seq:(Medium) rs1480217059 Functional Loss SNV dbSNP153 33..33 33 - - - 58949 RMVar_ID_58949 Human_SNP_ID_704603855 m1A Human chr22 - 41675096 41675096 41675096 GATCATTCTGCACCTGCCGCTGCTGTGTGAAGACAAGAATGTGCCCTACGTGTTTGTGCGCTCCA GATCATTCTGCACCTGCCGCTGCTGTGTGAAGTCAAGAATGTGCCCTACGTGTTTGTGCGCTCCA T A SNU13 Ensembl:ENSG00000100138 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41674895..41675213 26863196 MeRIP-seq:(Medium) rs752434289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65019,Human_RBP_ID_581716,Human_RBP_ID_931666,Human_RBP_ID_1101666,Human_RBP_ID_1612861,Human_RBP_ID_1943851,Human_RBP_ID_3674160,Human_RBP_ID_7087568,Human_RBP_ID_8551586,Human_RBP_ID_9127081,Human_RBP_ID_14509279,Human_RBP_ID_18194157,Human_RBP_ID_18790539,Human_RBP_ID_22086609,Human_RBP_ID_22454726,Human_RBP_ID_22508177,Human_RBP_ID_23950342,Human_RBP_ID_26823298,Human_RBP_ID_27494836 Human_Splice_Rec_2171194,Human_Splice_Rec_2171196,Human_Splice_Rec_2171202,Human_Splice_Rec_2171206,Human_Splice_Rec_2171212,Human_Splice_Rec_2171218,Human_Splice_Rec_2171226,Human_Splice_Rec_2171230,Human_Splice_Rec_2171236,Human_Splice_Rec_2171242,Human_Splice_Rec_2171248 RMVar_hsa_circ_85280,RMVar_hsa_circ_121890,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_214713,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 58950 RMVar_ID_58950 Human_SNP_ID_704607540 m1A Human chr22 - 41688731 41688731 41688731 AAGCGGGAGACTCAGGGTTGCGTTCACTCCCTAGCCTGTTAGATGGAGGCTTAGAGCCTGCGCCG AAGCGGGAGACTCAGGGTTGCGTTCACTCCCTGGCCTGTTAGATGGAGGCTTAGAGCCTGCGCCG T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41688727..41688816 26863196 MeRIP-seq:(Medium) rs1424172738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387431,Human_RBP_ID_19112257 RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 58951 RMVar_ID_58951 Human_SNP_ID_704607544 m1A Human chr22 + 41688746 41688746 41688746 GCCTCCATCTAACAGGCTAGGGAGTGAACGCAACCCTGAGTCTCCCGCTTCCCGGTCCCTCGGCC GCCTCCATCTAACAGGCTAGGGAGTGAACGCAGCCCTGAGTCTCCCGCTTCCCGGTCCCTCGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41688744..41688875 26863196 MeRIP-seq:(Medium) rs770654443 Functional Loss SNV dbSNP153 33..33 33 - - - 58952 RMVar_ID_58952 Human_SNP_ID_704609580 m1A Human chr22 + 41695929 41695929 41695929 GGAGCTGATTGGAAAGGATGTTGCAGAAAATCAGGCATCAGAGAAGAGAAACCAGAGAGAGGTTG GGAGCTGATTGGAAAGGATGTTGCAGAAAATCGGGCATCAGAGAAGAGAAACCAGAGAGAGGTTG A G C22orf46 Ensembl:ENSG00000184208 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41695514..41696432 26863196 MeRIP-seq:(Medium) rs932378959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5101277 58953 RMVar_ID_58953 Human_SNP_ID_704609919 m1A Human chr22 + 41697325 41697325 41697325 AACCACAGGAGATCCAGGAAGCGCTTGCTAGGACCAAGCTCCCAGCTCCCAGGACCCCCAGGCCG AACCACAGGAGATCCAGGAAGCGCTTGCTAGGCCCAAGCTCCCAGCTCCCAGGACCCCCAGGCCG A C C22orf46 Ensembl:ENSG00000184208 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41697308..41697419 26863196 MeRIP-seq:(Medium) rs956582205 Functional Loss SNV dbSNP153 33..33 33 - - - 58954 RMVar_ID_58954 Human_SNP_ID_704609920 m1A Human chr22 + 41697325 41697325 41697325 AACCACAGGAGATCCAGGAAGCGCTTGCTAGGACCAAGCTCCCAGCTCCCAGGACCCCCAGGCCG AACCACAGGAGATCCAGGAAGCGCTTGCTAGGGCCAAGCTCCCAGCTCCCAGGACCCCCAGGCCG A G C22orf46 Ensembl:ENSG00000184208 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41697308..41697419 26863196 MeRIP-seq:(Medium) rs956582205 Functional Loss SNV dbSNP153 33..33 33 - - - 58955 RMVar_ID_58955 Human_SNP_ID_704641622 m1A Human chr22 + 41813339 41813339 41813339 GGTGCTGCGCTTCCCGAGGATTGTGCACTATTACTTTGACCACAACTCCAACTGGAACCTCCTCA GGTGCTGCGCTTCCCGAGGATTGTGCACTATTGCTTTGACCACAACTCCAACTGGAACCTCCTCA A G CCDC134 Ensembl:ENSG00000100147 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:41810267..41813338 32194978 MeRIP-seq:(Medium) rs1208713458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4701491,Human_RBP_ID_22768156,Human_RBP_ID_22821196,Human_RBP_ID_27494859 Human_Splice_Rec_2171526 RMVar_hsa_circ_278300,RMVar_hsa_circ_280275,RMVar_hsa_circ_214719,RMVar_hsa_circ_214721,RMVar_hsa_circ_119134,RMVar_hsa_circ_214720,RMVar_hsa_circ_92933,RMVar_hsa_circ_86991,RMVar_hsa_circ_214727,RMVar_hsa_circ_214728,RMVar_hsa_circ_326384 58956 RMVar_ID_58956 Human_SNP_ID_704643518 m1A Human chr22 - 41820980 41820980 41820980 GCTTCCTCCTCAGTCCTTCAACCTCTATCTCCAGCCCCATCCCAGGCCTCAGTCCTCAGACTGCT GCTTCCTCCTCAGTCCTTCAACCTCTATCTCCGGCCCCATCCCAGGCCTCAGTCCTCAGACTGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41820855..41821221 26863196 MeRIP-seq:(Medium) rs1270811568 Functional Loss SNV dbSNP153 33..33 33 - - - 58957 RMVar_ID_58957 Human_SNP_ID_704644605 m1A Human chr22 + 41825856 41825856 41825856 CCCTGGAGCAGCTCAGGGCTCAGGGGGCCACAAGGAGGCAGGTCGGGAGGAAGAAGAGGTGGAGG CCCTGGAGCAGCTCAGGGCTCAGGGGGCCACAGGGAGGCAGGTCGGGAGGAAGAAGAGGTGGAGG A G CCDC134 Ensembl:ENSG00000100147 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41825706..41825867 26863196 MeRIP-seq:(Medium) rs949584341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27494860 RMVar_hsa_circ_214719,RMVar_hsa_circ_119134,RMVar_hsa_circ_92933,RMVar_hsa_circ_214728 58958 RMVar_ID_58958 Human_SNP_ID_704644607 m1A Human chr22 + 41825859 41825859 41825859 TGGAGCAGCTCAGGGCTCAGGGGGCCACAAGGAGGCAGGTCGGGAGGAAGAAGAGGTGGAGGTGT TGGAGCAGCTCAGGGCTCAGGGGGCCACAAGGGGGCAGGTCGGGAGGAAGAAGAGGTGGAGGTGT A G CCDC134 Ensembl:ENSG00000100147 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41825712..41826038 26863196 MeRIP-seq:(Medium) rs1291796193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27494860 RMVar_hsa_circ_214719,RMVar_hsa_circ_119134,RMVar_hsa_circ_92933,RMVar_hsa_circ_214728 58959 RMVar_ID_58959 Human_SNP_ID_704646338 m1A Human chr22 - 41832952 41832952 41832952 GTGCGTGGGGTGATGGCGCGTCATCGATCAGCAGCTCAGATTTGCATAGTGAGGTCCCTCCCCCC GTGCGTGGGGTGATGGCGCGTCATCGATCAGCTGCTCAGATTTGCATAGTGAGGTCCCTCCCCCC T A SREBF2-AS1 Ensembl:ENSG00000184068 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41832857..41832958 26863196 MeRIP-seq:(Medium) rs1160657817 Functional Loss SNV dbSNP153 33..33 33 - - - 58960 RMVar_ID_58960 Human_SNP_ID_704646339 m1A Human chr22 - 41832952 41832952 41832952 GTGCGTGGGGTGATGGCGCGTCATCGATCAGCAGCTCAGATTTGCATAGTGAGGTCCCTCCCCCC GTGCGTGGGGTGATGGCGCGTCATCGATCAGCCGCTCAGATTTGCATAGTGAGGTCCCTCCCCCC T G SREBF2-AS1 Ensembl:ENSG00000184068 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41832857..41832958 26863196 MeRIP-seq:(Medium) rs1160657817 Functional Loss SNV dbSNP153 33..33 33 - - - 58961 RMVar_ID_58961 Human_SNP_ID_704646447 m1A Human chr22 - 41833169 41833169 41833169 CCGCCCATGACACCCGACAACCCCCGCCCGGCACCGCCTCACCGACGGGTGCCACCCGCCGCCAT CCGCCCATGACACCCGACAACCCCCGCCCGGCGCCGCCTCACCGACGGGTGCCACCCGCCGCCAT T C SREBF2-AS1 Ensembl:ENSG00000184068 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:41833101..41867287;chr22:41833126..41833375;chr22:41833101..41867300;chr22:41833101..41867250 26863196 MeRIP-seq:(Medium) rs1301101035 Functional Loss SNV dbSNP153 33..33 33 - - - 58962 RMVar_ID_58962 Human_SNP_ID_704646488 m1A Human chr22 + 41833243 41833242 41833243 CACCGCCCCCGCGTCTCCCTGAGCGGGACGGCAGGGGGGGCTTCTGCGCTGAGCCGGGCGATGGA CACCGCCCCCGCGTCTCCCTGAGCGGGACGGC_GGGGGGGCTTCTGCGCTGAGCCGGGCGATGGA CA C SREBF2 Ensembl:ENSG00000198911 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:41833145..41833288 26863196 MeRIP-seq:(Medium) rs1372970812 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_833855,Human_RBP_ID_3962468,Human_RBP_ID_4701616,Human_RBP_ID_5324215,Human_RBP_ID_9332888,Human_RBP_ID_9433233,Human_RBP_ID_14509993,Human_RBP_ID_22087208,Human_RBP_ID_23950420,Human_RBP_ID_26789370 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 58963 RMVar_ID_58963 Human_SNP_ID_704646508 m1A Human chr22 + 41833271 41833271 41833271 CGGCAGGGGGGGCTTCTGCGCTGAGCCGGGCGATGGACGACAGCGGCGAGCTGGGTGGTCTGGAG CGGCAGGGGGGGCTTCTGCGCTGAGCCGGGCGGTGGACGACAGCGGCGAGCTGGGTGGTCTGGAG A G SREBF2 Ensembl:ENSG00000198911 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:41833185..41833287 26863410 MeRIP-seq:(Medium) rs1206392224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246339,Human_RBP_ID_833855,Human_RBP_ID_3962468,Human_RBP_ID_4701616,Human_RBP_ID_5324215,Human_RBP_ID_9332889,Human_RBP_ID_14509994,Human_RBP_ID_20769741,Human_RBP_ID_22087208,Human_RBP_ID_23015278,Human_RBP_ID_23950420,Human_RBP_ID_26789370 Human_Splice_Rec_2171533,Human_Splice_Rec_2171571,Human_Splice_Rec_2171607 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 58964 RMVar_ID_58964 Human_SNP_ID_704657839 m1A Human chr22 + 41875579 41875579 41875579 TCTAAAGGGCATCGACCTAGGCAGTCTGGTGGACAATGAGGTGGACCTGAAGATCGAGGACTTTA TCTAAAGGGCATCGACCTAGGCAGTCTGGTGGGCAATGAGGTGGACCTGAAGATCGAGGACTTTA A G SREBF2 Ensembl:ENSG00000198911 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs764787195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1612946,Human_RBP_ID_1943914,Human_RBP_ID_3674250,Human_RBP_ID_3963353,Human_RBP_ID_5203062,Human_RBP_ID_5599503,Human_RBP_ID_7088116,Human_RBP_ID_9393064,Human_RBP_ID_14510972,Human_RBP_ID_27821373 Human_Splice_Rec_2171544,Human_Splice_Rec_2171582,Human_Splice_Rec_2171618,Human_Splice_Rec_2171652 RMVar_hsa_circ_9595,RMVar_hsa_circ_24121,RMVar_hsa_circ_122139,RMVar_hsa_circ_39627,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729,RMVar_hsa_circ_29319,RMVar_hsa_circ_354754,RMVar_hsa_circ_355447,RMVar_hsa_circ_37548,RMVar_hsa_circ_214734,RMVar_hsa_circ_293282,RMVar_hsa_circ_214733,RMVar_hsa_circ_125188,RMVar_hsa_circ_335945,RMVar_hsa_circ_348704,RMVar_hsa_circ_354402,RMVar_hsa_circ_334403,RMVar_hsa_circ_45165,RMVar_hsa_circ_214736,RMVar_hsa_circ_214737,RMVar_hsa_circ_214735,RMVar_hsa_circ_41927,RMVar_hsa_circ_302948,RMVar_hsa_circ_338016,RMVar_hsa_circ_368734,RMVar_hsa_circ_326827,RMVar_hsa_circ_65348,RMVar_hsa_circ_214738,RMVar_hsa_circ_214739 58965 RMVar_ID_58965 Human_SNP_ID_704662406 m1A Human chr22 - 41893298 41893298 41893298 TTGCATGGCTTTCTCCAATTCTGAATGGCTCCAAGGTATTCTCACCTGGGTTCCTCTGGGCACAG TTGCATGGCTTTCTCCAATTCTGAATGGCTCCGAGGTATTCTCACCTGGGTTCCTCTGGGCACAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:41893276..41893300 26863196 MeRIP-seq:(Medium) rs754580493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214744 58966 RMVar_ID_58966 Human_SNP_ID_704664019 m1A Human chr22 + 41899082 41899082 41899082 CATGGCGCCACAGGCTGAAAAGAAGAGACGAGAGCAGTGTGGCCCCCAGCATCTTCAGAAGCTTT CATGGCGCCACAGGCTGAAAAGAAGAGACGAGGGCAGTGTGGCCCCCAGCATCTTCAGAAGCTTT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:41899031..41899158 26863196 MeRIP-seq:(Medium) rs1259817335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14511195 RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_88010,RMVar_hsa_circ_214734,RMVar_hsa_circ_354402,RMVar_hsa_circ_45165,RMVar_hsa_circ_214741,RMVar_hsa_circ_285826,RMVar_hsa_circ_214748,RMVar_hsa_circ_346387 58967 RMVar_ID_58967 Human_SNP_ID_704664602 m1A Human chr22 - 41901077 41901077 41901077 GGGCCCCAACAGTGGCAGCAGTGCCCTCTATCAGGATCCCCTCCCCCACCTGATAGGGCCTTCAG GGGCCCCAACAGTGGCAGCAGTGCCCTCTATCGGGATCCCCTCCCCCACCTGATAGGGCCTTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41901074..41901156 26863196 MeRIP-seq:(Medium) rs911711685 Functional Loss SNV dbSNP153 33..33 33 - - - 58968 RMVar_ID_58968 Human_SNP_ID_704666026 m1A Human chr22 - 41905699 41905686 41905700 TCAGCGGGAAGATGCTGAGGGGGAGAGAGAGAAATCGAGAGAGAGGTGGAGGGGTGGGCTGAGCC TCAGCGGGAAGATGCTGAGGGGGAGAGAGAG______________GTGGAGGGGTGGGCTGAGCC CCTCTCTCTCGATTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41905649..41905888 26863196 MeRIP-seq:(Medium) rs763613865 Functional Loss DEL dbSNP153 32..45 33 - - - 58969 RMVar_ID_58969 Human_SNP_ID_704668433 m1A Human chr22 - 41914199 41914199 41914199 GCGGCGTCGCAGCGCTGCTGGTGCTGGCCGGCATCGGGGCGCGCCTGGGACTGGAGAGGGCGCAC GCGGCGTCGCAGCGCTGCTGGTGCTGGCCGGCGTCGGGGCGCGCCTGGGACTGGAGAGGGCGCAC T C SHISA8 Ensembl:ENSG00000234965 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41911297..41914231 26863410 MeRIP-seq:(Medium) rs1460838753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2171693,Human_Splice_Rec_2171699 58970 RMVar_ID_58970 Human_SNP_ID_704671773 m1A Human chr22 - 41926204 41926192 41926204 CTCTTTGGCGCCCCCGCGCTGCTGGGCCTGGCACTGGTCCTGGCGCTGGTCCTGGTGGGTCTGGT CTCTTTGGCGCCCCCGCGCTGCTGGGCCTGGC____________GCTGGTCCTGGTGGGTCTGGT CGCCAGGACCAGT C TNFRSF13C Ensembl:ENSG00000159958 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41926153..41926292 26863196 MeRIP-seq:(Medium) rs776259962 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_17660034 58971 RMVar_ID_58971 Human_SNP_ID_704671778 m1A Human chr22 - 41926204 41926204 41926204 CTCTTTGGCGCCCCCGCGCTGCTGGGCCTGGCACTGGTCCTGGCGCTGGTCCTGGTGGGTCTGGT CTCTTTGGCGCCCCCGCGCTGCTGGGCCTGGCGCTGGTCCTGGCGCTGGTCCTGGTGGGTCTGGT T C TNFRSF13C Ensembl:ENSG00000159958 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41926153..41926292 26863196 MeRIP-seq:(Medium) rs778024793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17660034 58972 RMVar_ID_58972 Human_SNP_ID_704671915 m1A Human chr22 + 41926469 41926469 41926469 AGCCGGGGGGCGGTGGACAAGGGGAGGGAGAGAGGCGGCGGTGAGGGCCACGCGGTGATCGCGGG AGCCGGGGGGCGGTGGACAAGGGGAGGGAGAGGGGCGGCGGTGAGGGCCACGCGGTGATCGCGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:41926422..41926596 32194978 MeRIP-seq:(Medium) rs1268223591 Functional Loss SNV dbSNP153 33..33 33 - - - 58973 RMVar_ID_58973 Human_SNP_ID_704675809 m1A Human chr22 + 41940060 41940037 41940061 TCCAGCAGCTCCCCACCAGGCTCCACTGATCCAGCCCCACCATTCCTGATTTCTCCACCCCAACC TCCAGCAGCT________________________CCCCACCATTCCTGATTTCTCCACCCCAACC TCCCCACCAGGCTCCACTGATCCAG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:41939952..41940157 26863196 MeRIP-seq:(Medium) rs1183848283 Functional Loss DEL dbSNP153 11..34 33 - - - 58974 RMVar_ID_58974 Human_SNP_ID_704677607 m1A Human chr22 + 41946614 41946614 41946614 GATCGGGACACCGCCAGCAGGCGGCTCGGAGGACATTTCCCGAGAAGTGGACCCCGCGAAGCGGC GATCGGGACACCGCCAGCAGGCGGCTCGGAGGTCATTTCCCGAGAAGTGGACCCCGCGAAGCGGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41946605..41946705 26863196 MeRIP-seq:(Medium) rs773170192 Functional Loss SNV dbSNP153 33..33 33 - - - 58975 RMVar_ID_58975 Human_SNP_ID_704677805 m1A Human chr22 - 41947101 41947101 41947101 GGGCGGTTTGAAAGATCGGCGCGCACCGCAGGAGCAACGGTTGGTCCTGCGGCTGTGATGTCGGT GGGCGGTTTGAAAGATCGGCGCGCACCGCAGGGGCAACGGTTGGTCCTGCGGCTGTGATGTCGGT T C CENPM Ensembl:ENSG00000100162 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41947002..41947122 26863196 MeRIP-seq:(Medium) rs1569429425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708710 Human_Splice_Rec_2171721,Human_Splice_Rec_2171731,Human_Splice_Rec_2171747,Human_Splice_Rec_2171753 RMVar_hsa_circ_81164,RMVar_hsa_circ_214751,RMVar_hsa_circ_82669,RMVar_hsa_circ_214753 58976 RMVar_ID_58976 Human_SNP_ID_704685315 m1A Human chr22 - 41977011 41977011 41977011 CCTCCAGGGAGATGCTCCGGGCGCGGGGCTGCAAGGCTGAGCGGGGCGCGGGCTTCCCCGGGCCG CCTCCAGGGAGATGCTCCGGGCGCGGGGCTGCGAGGCTGAGCGGGGCGCGGGCTTCCCCGGGCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41976795..41977050 26863196 MeRIP-seq:(Medium) rs1211340098 Functional Loss SNV dbSNP153 33..33 33 - - - 58977 RMVar_ID_58977 Human_SNP_ID_704685337 m1A Human chr22 + 41977065 41977065 41977065 CTCCCTGGAGGAACGGAGACAAAGGAGGATTCATGTCCAAAGGTAGGGCGGCCGGCCAGGCCACC CTCCCTGGAGGAACGGAGACAAAGGAGGATTCCTGTCCAAAGGTAGGGCGGCCGGCCAGGCCACC A C SEPTIN3 Ensembl:ENSG00000100167 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41976794..41977120 26863196 MeRIP-seq:(Medium) rs1333831995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2171789,Human_Splice_Rec_2171809,Human_Splice_Rec_2171827,Human_Splice_Rec_2171845 58978 RMVar_ID_58978 Human_SNP_ID_704690751 m1A Human chr22 + 41998832 41998831 41998832 GCAGGAGGCCCGAAGCAAGATGGCGGTGAATCAGAGCCACACCGAGAACCGCCGCGGAGCCCTCA GCAGGAGGCCCGAAGCAAGATGGCGGTGAATC_GAGCCACACCGAGAACCGCCGCGGAGCCCTCA CA C WBP2NL Ensembl:ENSG00000183066 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41998808..41999010 26863196 MeRIP-seq:(Medium) rs1239603528 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2171869,Human_Splice_Rec_2171885,Human_Splice_Rec_2171899,Human_Splice_Rec_2171915,Human_Splice_Rec_2171921,Human_Splice_Rec_2171931,Human_Splice_Rec_2171937 58979 RMVar_ID_58979 Human_SNP_ID_704690753 m1A Human chr22 + 41998832 41998832 41998832 GCAGGAGGCCCGAAGCAAGATGGCGGTGAATCAGAGCCACACCGAGAACCGCCGCGGAGCCCTCA GCAGGAGGCCCGAAGCAAGATGGCGGTGAATCGGAGCCACACCGAGAACCGCCGCGGAGCCCTCA A G WBP2NL Ensembl:ENSG00000183066 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41998808..41999010 26863196 MeRIP-seq:(Medium) rs540233537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2171869,Human_Splice_Rec_2171885,Human_Splice_Rec_2171899,Human_Splice_Rec_2171915,Human_Splice_Rec_2171921,Human_Splice_Rec_2171931,Human_Splice_Rec_2171937 58980 RMVar_ID_58980 Human_SNP_ID_704690775 m1A Human chr22 + 41998857 41998857 41998857 GTGAATCAGAGCCACACCGAGAACCGCCGCGGAGCCCTCATCCCTAACGGTGAAAGGTGCCTGAG GTGAATCAGAGCCACACCGAGAACCGCCGCGGGGCCCTCATCCCTAACGGTGAAAGGTGCCTGAG A G WBP2NL Ensembl:ENSG00000183066 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41998808..41998963 26863196 MeRIP-seq:(Medium) rs1194220553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2171869,Human_Splice_Rec_2171885,Human_Splice_Rec_2171899,Human_Splice_Rec_2171915,Human_Splice_Rec_2171921,Human_Splice_Rec_2171931,Human_Splice_Rec_2171937 58981 RMVar_ID_58981 Human_SNP_ID_704710192 m1A Human chr22 - 42074343 42074343 42074343 ACCTCCTCCCGGAGCCCGCCGGGCCCACTCTCACCTCCCGCCGCCGATCGCACCGAAGCCCAAGA ACCTCCTCCCGGAGCCCGCCGGGCCCACTCTCGCCTCCCGCCGCCGATCGCACCGAAGCCCAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42074303..42074394 26863196 MeRIP-seq:(Medium) rs1362715165 Functional Loss SNV dbSNP153 33..33 33 - - - 58982 RMVar_ID_58982 Human_SNP_ID_704711670 m1A Human chr22 + 42079759 42079759 42079759 CGGTGGGGTGCGGGTGCCCGGGTGAGGGGCGGAGCTGGGGGCATGGCGTCCGGAGCGGCTCGCTG CGGTGGGGTGCGGGTGCCCGGGTGAGGGGCGGGGCTGGGGGCATGGCGTCCGGAGCGGCTCGCTG A G SMDT1 Ensembl:ENSG00000183172 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:42079701..42079925;chr22:42079690..42079975 26863196 MeRIP-seq:(Medium) rs1293093780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676149,Human_RBP_ID_4708286,Human_RBP_ID_5119952,Human_RBP_ID_5324245,Human_RBP_ID_8235608,Human_RBP_ID_8943296,Human_RBP_ID_9332898,Human_RBP_ID_9354237,Human_RBP_ID_9433235,Human_RBP_ID_17671127,Human_RBP_ID_22455289,Human_RBP_ID_23950713 58983 RMVar_ID_58983 Human_SNP_ID_704711673 m1A Human chr22 - 42079762 42079762 42079762 AGCCAGCGAGCCGCTCCGGACGCCATGCCCCCAGCTCCGCCCCTCACCCGGGCACCCGCACCCCA AGCCAGCGAGCCGCTCCGGACGCCATGCCCCCGGCTCCGCCCCTCACCCGGGCACCCGCACCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42079701..42079975 26863196 MeRIP-seq:(Medium) rs1413420179 Functional Loss SNV dbSNP153 33..33 33 - - - 58984 RMVar_ID_58984 Human_SNP_ID_704711674 m1A Human chr22 - 42079762 42079762 42079762 AGCCAGCGAGCCGCTCCGGACGCCATGCCCCCAGCTCCGCCCCTCACCCGGGCACCCGCACCCCA AGCCAGCGAGCCGCTCCGGACGCCATGCCCCCCGCTCCGCCCCTCACCCGGGCACCCGCACCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42079701..42079975 26863196 MeRIP-seq:(Medium) rs1413420179 Functional Loss SNV dbSNP153 33..33 33 - - - 58985 RMVar_ID_58985 Human_SNP_ID_704711752 m1A Human chr22 + 42079889 42079889 42079889 ATGTCTCCGCCGCATGGAGCGGCTCAGGCCGGAGCCTGGTACCGTCGAGGTCAGTCATCGTTACC ATGTCTCCGCCGCATGGAGCGGCTCAGGCCGGGGCCTGGTACCGTCGAGGTCAGTCATCGTTACC A G SMDT1 Ensembl:ENSG00000183172 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:42079838..42082106 32194978 MeRIP-seq:(Medium) rs376151257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582015,Human_RBP_ID_4708714,Human_RBP_ID_5203449,Human_RBP_ID_17702188,Human_RBP_ID_26822628 Human_Splice_Rec_2172029,Human_Splice_Rec_2172033,Human_Splice_Rec_2172035 58986 RMVar_ID_58986 Human_SNP_ID_704714889 m1A Human chr22 - 42090717 42090717 42090717 GCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTACTTCTACCGCCAGCACCTTCGTGAAGCCCATT GCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTGCTTCTACCGCCAGCACCTTCGTGAAGCCCATT T C NDUFA6 Ensembl:ENSG00000184983 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42090567..42090775 26863196 MeRIP-seq:(Medium) rs1200187280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1613070,Human_RBP_ID_4708287,Human_RBP_ID_18423659,Human_RBP_ID_22086625,Human_RBP_ID_22271494,Human_RBP_ID_22454504,Human_RBP_ID_23212808,Human_RBP_ID_26823317 Human_miRNA_ID_2144245,Human_miRNA_ID_2145774,Human_miRNA_ID_2688277 RMVar_hsa_circ_92591,RMVar_hsa_circ_214775 58987 RMVar_ID_58987 Human_SNP_ID_704714890 m1A Human chr22 - 42090717 42090717 42090717 GCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTACTTCTACCGCCAGCACCTTCGTGAAGCCCATT GCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTCCTTCTACCGCCAGCACCTTCGTGAAGCCCATT T G NDUFA6 Ensembl:ENSG00000184983 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42090567..42090775 26863196 MeRIP-seq:(Medium) rs1200187280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1613070,Human_RBP_ID_4708287,Human_RBP_ID_18423659,Human_RBP_ID_22086625,Human_RBP_ID_22271494,Human_RBP_ID_22454504,Human_RBP_ID_23212808,Human_RBP_ID_26823317 Human_miRNA_ID_2144245,Human_miRNA_ID_2145774,Human_miRNA_ID_2688277 RMVar_hsa_circ_92591,RMVar_hsa_circ_214775 58988 RMVar_ID_58988 Human_SNP_ID_704714895 m1A Human chr22 - 42090721 42090721 42090721 TTTGGCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTACTTCTACCGCCAGCACCTTCGTGAAGCC TTTGGCAAGATGGCGGGGAGCGGCGTCCGCCATGCTACTTCTACCGCCAGCACCTTCGTGAAGCC T A NDUFA6 Ensembl:ENSG00000184983 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42090567..42090775 26863196 MeRIP-seq:(Medium) rs1269911566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582053,Human_RBP_ID_781692,Human_RBP_ID_833713,Human_RBP_ID_4708287,Human_RBP_ID_18423659,Human_RBP_ID_22086625,Human_RBP_ID_22454504,Human_RBP_ID_23212808,Human_RBP_ID_23950752,Human_RBP_ID_26823317 RMVar_hsa_circ_92591,RMVar_hsa_circ_214775 58989 RMVar_ID_58989 Human_SNP_ID_704714896 m1A Human chr22 - 42090721 42090721 42090721 TTTGGCAAGATGGCGGGGAGCGGCGTCCGCCAAGCTACTTCTACCGCCAGCACCTTCGTGAAGCC TTTGGCAAGATGGCGGGGAGCGGCGTCCGCCAGGCTACTTCTACCGCCAGCACCTTCGTGAAGCC T C NDUFA6 Ensembl:ENSG00000184983 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42090567..42090775 26863196 MeRIP-seq:(Medium) rs1269911566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582053,Human_RBP_ID_781692,Human_RBP_ID_833713,Human_RBP_ID_4708287,Human_RBP_ID_18423659,Human_RBP_ID_22086625,Human_RBP_ID_22454504,Human_RBP_ID_23212808,Human_RBP_ID_23950752,Human_RBP_ID_26823317 RMVar_hsa_circ_92591,RMVar_hsa_circ_214775 58990 RMVar_ID_58990 Human_SNP_ID_704714906 m1A Human chr22 + 42090728 42090728 42090728 CGAAGGTGCTGGCGGTAGAAGTAGCTTGGCGGACGCCGCTCCCCGCCATCTTGCCAAAGCATCCA CGAAGGTGCTGGCGGTAGAAGTAGCTTGGCGGCCGCCGCTCCCCGCCATCTTGCCAAAGCATCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42090536..42090775 26863196 MeRIP-seq:(Medium) rs371574739 Functional Loss SNV dbSNP153 33..33 33 - - - 58991 RMVar_ID_58991 Human_SNP_ID_704722191 m1A Human chr22 + 42119162 42119161 42119163 AGAGAGACAAAGAGAGATAGAGAGACAGAAACAGATACAGAGACAGAGTTAGAGATACAGAGAGA AGAGAGACAAAGAGAGATAGAGAGACAGAAAC__ATACAGAGACAGAGTTAGAGATACAGAGAGA CAG C NDUFA6-DT Ensembl:ENSG00000237037 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42119152..42119488 26863196 MeRIP-seq:(Medium) rs1426734996 Functional Loss DEL dbSNP153 33..34 33 - - - 58992 RMVar_ID_58992 Human_SNP_ID_704736924 m1A Human chr22 + 42160420 42160420 42160420 TGCCTACAGCTCACACTGCCAGCTCTGGCAACACAGGCCTGGACCTCCTCCCATCCCCACGGGTC TGCCTACAGCTCACACTGCCAGCTCTGGCAACGCAGGCCTGGACCTCCTCCCATCCCCACGGGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:42160371..42160473 32194978 MeRIP-seq:(Medium) rs1276573243 Functional Loss SNV dbSNP153 33..33 33 - - - 58993 RMVar_ID_58993 Human_SNP_ID_704755286 m1A Human chr22 - 42222373 42222373 42222373 TGAAAATGACAGTGACGAGAATGGAATGGGAAAGGACAAATACAGGAAGGAGAGTAGTGTCATGA TGAAAATGACAGTGACGAGAATGGAATGGGAAGGGACAAATACAGGAAGGAGAGTAGTGTCATGA T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42222370..42222606 26863196 MeRIP-seq:(Medium) rs141381238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14513029 58994 RMVar_ID_58994 Human_SNP_ID_704769321 m1A Human chr22 + 42270005 42270000 42270005 GCCGCCCGCTCACACCCGCCGCCTTTGCACCCAAGGCCTCGCGCGACCAGCAGGTAGACCTTCCC GCCGCCCGCTCACACCCGCCGCCTTTGC_____AGGCCTCGCGCGACCAGCAGGTAGACCTTCCC CACCCA C OGFRP1 Ensembl:ENSG00000182057 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42270003..42270343 26863196 MeRIP-seq:(Medium) rs1322172493 Functional Loss DEL dbSNP153 29..33 33 - - - Human_Splice_Rec_2172363,Human_Splice_Rec_2172365,Human_Splice_Rec_2172367,Human_Splice_Rec_2172373 58995 RMVar_ID_58995 Human_SNP_ID_704769578 m1A Human chr22 + 42270590 42270590 42270590 GGCTCCCCTGGCGGAGGCCGCGGCCGCCTCGCAGGGGCCGAAAGCGGCTGGGCTCGGGGTTTTTT GGCTCCCCTGGCGGAGGCCGCGGCCGCCTCGCTGGGGCCGAAAGCGGCTGGGCTCGGGGTTTTTT A T OGFRP1 Ensembl:ENSG00000182057 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42270465..42270628 26863196 MeRIP-seq:(Medium) rs1201136994 Functional Loss SNV dbSNP153 33..33 33 - - - 58996 RMVar_ID_58996 Human_SNP_ID_704769600 m1A Human chr22 - 42270621 42270621 42270621 GTTATTTCCTGTGTGTTGGGAGAATGGAGAGAAAAAACCCCGAGCCCAGCCGCTTTCGGCCCCTG GTTATTTCCTGTGTGTTGGGAGAATGGAGAGAGAAAACCCCGAGCCCAGCCGCTTTCGGCCCCTG T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42270473..42270632 26863196 MeRIP-seq:(Medium) rs1473717760 Functional Loss SNV dbSNP153 33..33 33 - - - 58997 RMVar_ID_58997 Human_SNP_ID_704781292 m1A Human chr22 + 42317026 42317026 42317026 TTTGCTGCCAAGTGGACTCTGGCATGGCCGTAAGGCATCTTCAATGGTCCCATGTCCTCAACACT TTTGCTGCCAAGTGGACTCTGGCATGGCCGTACGGCATCTTCAATGGTCCCATGTCCTCAACACT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42316815..42317035 26863196 MeRIP-seq:(Medium) rs1404318247 Functional Loss SNV dbSNP153 33..33 33 - - - 58998 RMVar_ID_58998 Human_SNP_ID_704781317 m1A Human chr22 - 42317136 42317136 42317136 GAAGGTGGGGTGAGTCAGACGTGGCCAAGCACACAGAGCGCTCAGTCTGCAGGGGAGGCAGACGG GAAGGTGGGGTGAGTCAGACGTGGCCAAGCACGCAGAGCGCTCAGTCTGCAGGGGAGGCAGACGG T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42317088..42317174 26863196 MeRIP-seq:(Medium) rs1455258842 Functional Loss SNV dbSNP153 33..33 33 - - - 58999 RMVar_ID_58999 Human_SNP_ID_704786780 m1A Human chr22 - 42337459 42337459 42337459 TTGGAGGTACAAAAGCACAGGATGAGGGGGACACCAAGCATTGGCAGTGGCACCAGGGCTTGTAA TTGGAGGTACAAAAGCACAGGATGAGGGGGACGCCAAGCATTGGCAGTGGCACCAGGGCTTGTAA T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42337183..42337533 26863196 MeRIP-seq:(Medium) rs554633301 Functional Loss SNV dbSNP153 33..33 33 - - - 59000 RMVar_ID_59000 Human_SNP_ID_704793728 m1A Human chr22 + 42364673 42364673 42364673 CGGATTTCTTTGTGGCATCCACTTCATCGCTCAGCAGCCAGCCATGATGTCATAAGCCCATCAGA CGGATTTCTTTGTGGCATCCACTTCATCGCTCGGCAGCCAGCCATGATGTCATAAGCCCATCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42364622..42364759 26863196 MeRIP-seq:(Medium) rs372765637 Functional Loss SNV dbSNP153 33..33 33 - - - 59001 RMVar_ID_59001 Human_SNP_ID_704794761 m1A Human chr22 - 42369144 42369144 42369144 GGGACAGCCACGTGGCCGCAGGAGGATTTACAACATTTTCTTTCGCCATCGATGTTATCGCAAAA GGGACAGCCACGTGGCCGCAGGAGGATTTACAGCATTTTCTTTCGCCATCGATGTTATCGCAAAA T C LINC01315 Ensembl:ENSG00000229891 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42369094..42369178 26863196 MeRIP-seq:(Medium) rs1172764466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23285708 Human_Splice_Rec_2172379,Human_Splice_Rec_2172383 59002 RMVar_ID_59002 Human_SNP_ID_704834515 m1A Human chr22 - 42512864 42512864 42512864 CAGTGAATGGCTGGAGGTGCAGGGCCAGGAGGAGGCGAGGCAGGGCCTGCAGCGGTCTCTGAGAG CAGTGAATGGCTGGAGGTGCAGGGCCAGGAGGCGGCGAGGCAGGGCCTGCAGCGGTCTCTGAGAG T G RRP7A Ensembl:ENSG00000189306 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:42512776..42514213 26863410 MeRIP-seq:(Medium) rs9745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246785,Human_RBP_ID_7088965,Human_RBP_ID_27309574 GWAS_ID_6865,GWAS_ID_6866,GWAS_ID_6867,GWAS_ID_6868,GWAS_ID_6869,GWAS_ID_6870,GWAS_ID_6871,GWAS_ID_6872,GWAS_ID_6873,GWAS_ID_6874,GWAS_ID_6875,GWAS_ID_6876,GWAS_ID_6877,GWAS_ID_6878,GWAS_ID_6879 59003 RMVar_ID_59003 Human_SNP_ID_704836671 m1A Human chr22 + 42518081 42518081 42518081 TCTGAGGCCAGGTGGACTTGGTGCCTTGTCGAACGCCGTGTGCTCTCACATAGAGGTAGTGAGAA TCTGAGGCCAGGTGGACTTGGTGCCTTGTCGATCGCCGTGTGCTCTCACATAGAGGTAGTGAGAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42518051..42518150 26863196 MeRIP-seq:(Medium) rs1231523270 Functional Loss SNV dbSNP153 33..33 33 - - - 59004 RMVar_ID_59004 Human_SNP_ID_704836704 m1A Human chr22 - 42518149 42518138 42518150 CCTGGCCATCCCTCCCCTCCCATTTCCTTTCCAGCTATTCCAATCAAGTTCTCTGAAAAGCAACA CCTGGCCATCCCTCCCCTCCCATTTCCTTTC____________TCAAGTTCTCTGAAAAGCAACA ATTGGAATAGCTG A RRP7A Ensembl:ENSG00000189306 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:42518101..42518208 26863410 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 32..43 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_214791 59005 RMVar_ID_59005 Human_SNP_ID_704837111 m1A Human chr22 + 42519419 42519419 42519419 GGCGATGAGAAGGGGATGGGCTCACCTGGACGAGCGGGTGTGGACGGAAATGGGTTTGTCCTGGG GGCGATGAGAAGGGGATGGGCTCACCTGGACGGGCGGGTGTGGACGGAAATGGGTTTGTCCTGGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:42519331..42519544 26863196 MeRIP-seq:(Medium) rs1276470848 Functional Loss SNV dbSNP153 33..33 33 - - - 59006 RMVar_ID_59006 Human_SNP_ID_704855160 m1A Human chr22 - 42573467 42573467 42573467 AGGCCAAGGTGGGCGGATCACGAGGTCAGGAGATCAAGAGCATCCTGGTTAAGACAGTGAAACCC AGGCCAAGGTGGGCGGATCACGAGGTCAGGAGCTCAAGAGCATCCTGGTTAAGACAGTGAAACCC T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42573459..42573646 26863196 MeRIP-seq:(Medium) rs550319121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2721078,Human_RBP_ID_10056427,Human_RBP_ID_18535531 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 59007 RMVar_ID_59007 Human_SNP_ID_704855182 m1A Human chr22 - 42573499 42573483 42573500 TCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGAGGCCAAGGTGGGCGGATCACGAGGTCAGGAGA TCCCAGCACTTTGGGAGGCCAAGGCAGGCGG_________________ATCACGAGGTCAGGAGA TCCGCCCACCTTGGCCTC T RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42573483..42573670 26863196 MeRIP-seq:(Medium) rs1045791101 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_3679219,Human_RBP_ID_7089025,Human_RBP_ID_8208779,Human_RBP_ID_14514419,Human_RBP_ID_17516020,Human_RBP_ID_21960380 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 59008 RMVar_ID_59008 Human_SNP_ID_704855198 m1A Human chr22 - 42573499 42573499 42573499 TCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGAGGCCAAGGTGGGCGGATCACGAGGTCAGGAGA TCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGTGGCCAAGGTGGGCGGATCACGAGGTCAGGAGA T A RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42573483..42573670 26863196 MeRIP-seq:(Medium) rs878991679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679219,Human_RBP_ID_7089025,Human_RBP_ID_8208779,Human_RBP_ID_14514419,Human_RBP_ID_17516020,Human_RBP_ID_21960380 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 59009 RMVar_ID_59009 Human_SNP_ID_704855199 m1A Human chr22 - 42573499 42573499 42573499 TCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGAGGCCAAGGTGGGCGGATCACGAGGTCAGGAGA TCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGGGGCCAAGGTGGGCGGATCACGAGGTCAGGAGA T C RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42573483..42573670 26863196 MeRIP-seq:(Medium) rs878991679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679219,Human_RBP_ID_7089025,Human_RBP_ID_8208779,Human_RBP_ID_14514419,Human_RBP_ID_17516020,Human_RBP_ID_21960380 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 59010 RMVar_ID_59010 Human_SNP_ID_704855239 m1A Human chr22 + 42573580 42573580 42573580 CTGCGCCCGGCCCTGTCTGGCTTCTTGAAGGCAGACACAAGTCTGCAGGCTGTTCACGCCCCCAT CTGCGCCCGGCCCTGTCTGGCTTCTTGAAGGCGGACACAAGTCTGCAGGCTGTTCACGCCCCCAT A G SERHL2 Ensembl:ENSG00000183569 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42573558..42573642 26863196 MeRIP-seq:(Medium) rs1251292368 Functional Loss SNV dbSNP153 33..33 33 - - - 59011 RMVar_ID_59011 Human_SNP_ID_704855932 m1A Human chr22 + 42574794 42574794 42574794 GCAGCAGCTCGATCCTCTGCTTGTCCTCCTCAAACTTCTTGCGCAGCTGCGCTAGATCTGGGGGT GCAGCAGCTCGATCCTCTGCTTGTCCTCCTCAGACTTCTTGCGCAGCTGCGCTAGATCTGGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42574676..42574836 26863196 MeRIP-seq:(Medium) rs1006213133 Functional Loss SNV dbSNP153 33..33 33 - - - 59012 RMVar_ID_59012 Human_SNP_ID_704858335 m1A Human chr22 + 42581979 42581979 42581979 TCGGGATACCGTCCTCCGGGTCCCGCGCCGCGAGCTTCGTCCTGCGCGCCACCATCTTGCCACCC TCGGGATACCGTCCTCCGGGTCCCGCGCCGCGCGCTTCGTCCTGCGCGCCACCATCTTGCCACCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:42581880..42581992;chr22:42581842..42581991;chr22:42581838..42581987;chr22:42581859..42582000 26863196 MeRIP-seq:(Medium) rs1170719206 Functional Loss SNV dbSNP153 33..33 33 - - - 59013 RMVar_ID_59013 Human_SNP_ID_704858336 m1A Human chr22 + 42581979 42581979 42581979 TCGGGATACCGTCCTCCGGGTCCCGCGCCGCGAGCTTCGTCCTGCGCGCCACCATCTTGCCACCC TCGGGATACCGTCCTCCGGGTCCCGCGCCGCGTGCTTCGTCCTGCGCGCCACCATCTTGCCACCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:42581880..42581992;chr22:42581842..42581991;chr22:42581838..42581987;chr22:42581859..42582000 26863196 MeRIP-seq:(Medium) rs1170719206 Functional Loss SNV dbSNP153 33..33 33 - - - 59014 RMVar_ID_59014 Human_SNP_ID_704862601 m1A Human chr22 - 42596233 42596233 42596233 TTCGAACAAAAGCCTTGACCAACATGTCCCGGACACTGGTGAACAAGGAAGAACCCCCCAAAGAG TTCGAACAAAAGCCTTGACCAACATGTCCCGGTCACTGGTGAACAAGGAAGAACCCCCCAAAGAG T A POLDIP3 Ensembl:ENSG00000100227 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:42596140..42596314;chr22:42596133..42596302 26863196 MeRIP-seq:(Medium) rs755283036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14514761,Human_RBP_ID_17399562,Human_RBP_ID_18790975 Human_Splice_Rec_2172739,Human_Splice_Rec_2172755,Human_Splice_Rec_2172769,Human_Splice_Rec_2172791,Human_Splice_Rec_2172811 Human_miRNA_ID_2176152,Human_miRNA_ID_2179597 RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_214797,RMVar_hsa_circ_290888,RMVar_hsa_circ_285350,RMVar_hsa_circ_352328,RMVar_hsa_circ_359823,RMVar_hsa_circ_314204,RMVar_hsa_circ_214801,RMVar_hsa_circ_39802,RMVar_hsa_circ_214800 59015 RMVar_ID_59015 Human_SNP_ID_704868471 m1A Human chr22 + 42614829 42614829 42614829 ACCGTCCTTTCGCCGCCGCCCCGCGCTTCCTGATGAGTTCGTCCAGGGAGATGTCCGCCATCTTG ACCGTCCTTTCGCCGCCGCCCCGCGCTTCCTGTTGAGTTCGTCCAGGGAGATGTCCGCCATCTTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42614816..42614906 26863196 MeRIP-seq:(Medium) rs774049574 Functional Loss SNV dbSNP153 33..33 33 - - - 59016 RMVar_ID_59016 Human_SNP_ID_704868513 m1A Human chr22 + 42614870 42614870 42614870 TCCAGGGAGATGTCCGCCATCTTGCTCCGCCGAGCAAGCCGAAAGCAGTCGAGACCCCGCGAGCC TCCAGGGAGATGTCCGCCATCTTGCTCCGCCGGGCAAGCCGAAAGCAGTCGAGACCCCGCGAGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42614736..42614898 26863196 MeRIP-seq:(Medium) rs1424757759 Functional Loss SNV dbSNP153 33..33 33 - - - 59017 RMVar_ID_59017 Human_SNP_ID_704868815 m1A Human chr22 + 42615286 42615286 42615286 CTTATGAGTAAGGAAAATAACGATTCGGGGTGACGCCCGAATCCTCACTGCTAATGTGAGACGAA CTTATGAGTAAGGAAAATAACGATTCGGGGTGGCGCCCGAATCCTCACTGCTAATGTGAGACGAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs995709174 Functional Loss SNV dbSNP153 33..33 33 - - - 59018 RMVar_ID_59018 Human_SNP_ID_704868844 m1A Human chr22 - 42615298 42615298 42615298 CCCGCTCAAAAATTCGTCTCACATTAGCAGTGAGGATTCGGGCGTCACCCCGAATCGTTATTTTC CCCGCTCAAAAATTCGTCTCACATTAGCAGTGCGGATTCGGGCGTCACCCCGAATCGTTATTTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42615278..42615430 26863196 MeRIP-seq:(Medium) rs1487875590 Functional Loss SNV dbSNP153 33..33 33 - - - 59019 RMVar_ID_59019 Human_SNP_ID_704870726 m1A Human chr22 + 42619497 42619497 42619497 CTCAGCCTTATAGTGTGTGTGGGGGGTGGACGAGGGGTCATGAGGACAGGGATGGGGCTGGGCGT CTCAGCCTTATAGTGTGTGTGGGGGGTGGACGTGGGGTCATGAGGACAGGGATGGGGCTGGGCGT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:42619476..42619500 26863196 MeRIP-seq:(Medium) rs1340350105 Functional Loss SNV dbSNP153 33..33 33 - - - 59020 RMVar_ID_59020 Human_SNP_ID_704870751 m1A Human chr22 - 42619583 42619583 42619583 CTTCGGGAGCAGGGCTGTGTCCCAGATGGGCCACGGCTGAGCCTTCAGAGTACGTCCTGCCTGGC CTTCGGGAGCAGGGCTGTGTCCCAGATGGGCCGCGGCTGAGCCTTCAGAGTACGTCCTGCCTGGC T C CYB5R3 Ensembl:ENSG00000100243 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42619533..42619885 26863196 MeRIP-seq:(Medium) rs1222672039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582204,Human_RBP_ID_782241,Human_RBP_ID_1029814,Human_RBP_ID_8864692,Human_RBP_ID_17287113,Human_RBP_ID_17400063,Human_RBP_ID_23951067 Human_miRNA_ID_940431 59021 RMVar_ID_59021 Human_SNP_ID_704870804 m1A Human chr22 - 42619731 42619731 42619731 ACGGTCACACGGCCACCCGCCCCGCGCACCCCACGCCCTGTTCACGCTCACCCAGTCACCTCCCC ACGGTCACACGGCCACCCGCCCCGCGCACCCCGCGCCCTGTTCACGCTCACCCAGTCACCTCCCC T C CYB5R3 Ensembl:ENSG00000100243 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:42619624..42619950 26863196 MeRIP-seq:(Medium) rs778448550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582213,Human_RBP_ID_17400064,Human_RBP_ID_26499303 Human_miRNA_ID_1420419,Human_miRNA_ID_1808056 59022 RMVar_ID_59022 Human_SNP_ID_704870814 m1A Human chr22 - 42619749 42619742 42619749 GTCTTCTGAGGGCCGGGCACGGTCACACGGCCACCCGCCCCGCGCACCCCACGCCCTGTTCACGC GTCTTCTGAGGGCCGGGCACGGTCACACGGCC_______CCGCGCACCCCACGCCCTGTTCACGC GGGCGGGT G CYB5R3 Ensembl:ENSG00000100243 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:42619701..42619950 26863196 MeRIP-seq:(Medium) rs1313801065 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_582213,Human_RBP_ID_17400064,Human_RBP_ID_17660326,Human_RBP_ID_27039679 59023 RMVar_ID_59023 Human_SNP_ID_704870890 m1A Human chr22 - 42619876 42619876 42619876 GATCCGGGACCACCTTCCACCCCCAGAGGAGGAGCCGCTGGTGCTGATGTGTGGCCCCCCACCCA GATCCGGGACCACCTTCCACCCCCAGAGGAGGCGCCGCTGGTGCTGATGTGTGGCCCCCCACCCA T G CYB5R3 Ensembl:ENSG00000100243 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:42619826..42619950 26863196 MeRIP-seq:(Medium) rs1474956002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582215,Human_RBP_ID_782243,Human_RBP_ID_9127223,Human_RBP_ID_21896847,Human_RBP_ID_22454506 Human_Splice_Rec_2172844,Human_Splice_Rec_2172860,Human_Splice_Rec_2172876,Human_Splice_Rec_2172890,Human_Splice_Rec_2172900,Human_Splice_Rec_2172918 59024 RMVar_ID_59024 Human_SNP_ID_704873084 m1A Human chr22 + 42627329 42627329 42627329 CACTGACCTGGTTGGCAAAGAGCAGGTGGCACACAGTGTGGTCATCAGGGTCCTTCATGATGGCG CACTGACCTGGTTGGCAAAGAGCAGGTGGCACGCAGTGTGGTCATCAGGGTCCTTCATGATGGCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:42627301..42627375 26863196 MeRIP-seq:(Medium) rs1055746009 Functional Loss SNV dbSNP153 33..33 33 - - - 59025 RMVar_ID_59025 Human_SNP_ID_704873262 m1A Human chr22 - 42627655 42627655 42627655 GAAGTTCGCCATCCGACCTGACAAAAAGTCCAACCCTATCATCAGGACAGTGAAGTCTGTGGGCA GAAGTTCGCCATCCGACCTGACAAAAAGTCCAGCCCTATCATCAGGACAGTGAAGTCTGTGGGCA T C CYB5R3 Ensembl:ENSG00000100243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42627566..42627720 26863196 MeRIP-seq:(Medium) rs908208949 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1029818,Human_RBP_ID_17987874,Human_RBP_ID_19009388,Human_RBP_ID_22455298,Human_RBP_ID_22674427 Human_Splice_Rec_2172838,Human_Splice_Rec_2172839,Human_Splice_Rec_2172854,Human_Splice_Rec_2172855,Human_Splice_Rec_2172870,Human_Splice_Rec_2172871,Human_Splice_Rec_2172884,Human_Splice_Rec_2172885,Human_Splice_Rec_2172894,Human_Splice_Rec_2172895,Human_Splice_Rec_2172912,Human_Splice_Rec_2172913,Human_Splice_Rec_2172928 RMVar_hsa_circ_68033,RMVar_hsa_circ_377343 59026 RMVar_ID_59026 Human_SNP_ID_704873527 m1A Human chr22 + 42628233 42628233 42628233 GTCTCCAATCTGCATGCTCTCCAGGTACTGAGACATCTTCCCTCCAGCGGGAAACTTGGGATGGG GTCTCCAATCTGCATGCTCTCCAGGTACTGAGGCATCTTCCCTCCAGCGGGAAACTTGGGATGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42628126..42628234 26863196 MeRIP-seq:(Medium) rs121965006 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_194 GWAS_ID_6880,GWAS_ID_6881,GWAS_ID_6882 59027 RMVar_ID_59027 Human_SNP_ID_704873558 m1A Human chr22 - 42628283 42628283 42628283 GCTGGGGACTGAGGGCTGCGGGGGTGTCTTGCAGGTTTACTTCAAGGACACCCATCCCAAGTTTC GCTGGGGACTGAGGGCTGCGGGGGTGTCTTGCGGGTTTACTTCAAGGACACCCATCCCAAGTTTC T C CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:42628251..42628425 26863196 MeRIP-seq:(Medium) rs373889804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19113618,Human_RBP_ID_22455055,Human_RBP_ID_22675787 RMVar_hsa_circ_68033,RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591 59028 RMVar_ID_59028 Human_SNP_ID_704873614 m1A Human chr22 - 42628398 42628398 42628398 TGACGGCTGGGTGGATGGGGCTCCACGGGAGAAGGCCATGTGTGGGCCTCAGAAGAAGCTGCAGA TGACGGCTGGGTGGATGGGGCTCCACGGGAGACGGCCATGTGTGGGCCTCAGAAGAAGCTGCAGA T G CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42628394..42628508 26863196 MeRIP-seq:(Medium) rs541928449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5388466 RMVar_hsa_circ_68033,RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591 59029 RMVar_ID_59029 Human_SNP_ID_704873962 m1A Human chr22 - 42629355 42629355 42629355 AGGTGAGATCTGGGGCTGAGTAGGCACTGACCAGGTGAAGAAGGAAGAAAAGGAGCTTCAGGTGC AGGTGAGATCTGGGGCTGAGTAGGCACTGACCCGGTGAAGAAGGAAGAAAAGGAGCTTCAGGTGC T G CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42629352..42629417 26863196 MeRIP-seq:(Medium) rs1417204022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68033,RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591 59030 RMVar_ID_59030 Human_SNP_ID_704874621 m1A Human chr22 - 42631440 42631440 42631440 GCAGCTTTGGGCCTCTCTCCAGATCATCAGCCATGACACCCGGCGCTTCCGCTTTGCCCTGCCGT GCAGCTTTGGGCCTCTCTCCAGATCATCAGCCGTGACACCCGGCGCTTCCGCTTTGCCCTGCCGT T C CYB5R3 Ensembl:ENSG00000100243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42631334..42631487 26863196 MeRIP-seq:(Medium) rs957453549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931925,Human_RBP_ID_4713866,Human_RBP_ID_9127224,Human_RBP_ID_26823328 Human_Splice_Rec_2172832,Human_Splice_Rec_2172833,Human_Splice_Rec_2172848,Human_Splice_Rec_2172849,Human_Splice_Rec_2172864,Human_Splice_Rec_2172865,Human_Splice_Rec_2172878,Human_Splice_Rec_2172879,Human_Splice_Rec_2172906,Human_Splice_Rec_2172907,Human_Splice_Rec_2172922,Human_Splice_Rec_2172923,Human_Splice_Rec_2172932 RMVar_hsa_circ_214807,RMVar_hsa_circ_68033,RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591,RMVar_hsa_circ_323576,RMVar_hsa_circ_352613 59031 RMVar_ID_59031 Human_SNP_ID_704876161 m1A Human chr22 - 42636837 42636837 42636837 CCCCGCGGGTCCTGTCGTTTCAGTTGGGCCATATGGTGCTCTTCCCAGTCTGGTTCCTGTACAGT CCCCGCGGGTCCTGTCGTTTCAGTTGGGCCATGTGGTGCTCTTCCCAGTCTGGTTCCTGTACAGT T C CYB5R3 Ensembl:ENSG00000100243 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:42636701..42636907 26863410 MeRIP-seq:(Medium) rs147001900 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_65154,Human_RBP_ID_246576,Human_RBP_ID_582230,Human_RBP_ID_1308314,Human_RBP_ID_2721111,Human_RBP_ID_4709141 Human_Splice_Rec_2172830,Human_Splice_Rec_2172846,Human_Splice_Rec_2172862,Human_Splice_Rec_2172904,Human_Splice_Rec_2172920,Human_Splice_Rec_2172930 Human_miRNA_ID_2301973,Human_miRNA_ID_2305235,Human_miRNA_ID_2308501 RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591,RMVar_hsa_circ_352613,RMVar_hsa_circ_214810,RMVar_hsa_circ_214809 59032 RMVar_ID_59032 Human_SNP_ID_704879783 m1A Human chr22 + 42648759 42648759 42648759 ATCCGGGTTCTGTTCCTTGTTGCTAAACGTGCAAAACCCTCTGACATAGTGACATCGCACACACA ATCCGGGTTCTGTTCCTTGTTGCTAAACGTGCGAAACCCTCTGACATAGTGACATCGCACACACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42648757..42649073 26863196 MeRIP-seq:(Medium) rs8190371 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - GWAS_ID_6883,GWAS_ID_6884,GWAS_ID_6885,GWAS_ID_6886,GWAS_ID_6887,GWAS_ID_6888,GWAS_ID_6889 59033 RMVar_ID_59033 Human_SNP_ID_704879787 m1A Human chr22 - 42648768 42648768 42648768 GAACGTGTGTGTGTGTGCGATGTCACTATGTCAGAGGGTTTTGCACGTTTAGCAACAAGGAACAG GAACGTGTGTGTGTGTGCGATGTCACTATGTCTGAGGGTTTTGCACGTTTAGCAACAAGGAACAG T A CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42648765..42649057 26863196 MeRIP-seq:(Medium) rs1395083768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5298308,Human_RBP_ID_5653484,Human_RBP_ID_7089213,Human_RBP_ID_14515219,Human_RBP_ID_17286803,Human_RBP_ID_23954864 59034 RMVar_ID_59034 Human_SNP_ID_704883628 m1A Human chr22 - 42662174 42662174 42662174 GAGCCGGCTGGACCCGCGCCCCGGGCGCCGGGAGCCTTTTCCTGGCTCGGGCGCGCCCCCTGGAG GAGCCGGCTGGACCCGCGCCCCGGGCGCCGGGCGCCTTTTCCTGGCTCGGGCGCGCCCCCTGGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42662152..42662251 26863196 MeRIP-seq:(Medium) rs141704414 Functional Loss SNV dbSNP153 33..33 33 - - - 59035 RMVar_ID_59035 Human_SNP_ID_704883668 m1A Human chr22 - 42662239 42662239 42662239 CTCGGCTGGAGCAGAGCAGCGGCAGAACCCCCAGCCGAAGCCGGTGGGAGTGGAGATTTCGGATG CTCGGCTGGAGCAGAGCAGCGGCAGAACCCCCGGCCGAAGCCGGTGGGAGTGGAGATTTCGGATG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:42662147..42662279 26863196 MeRIP-seq:(Medium) rs1404560740 Functional Loss SNV dbSNP153 33..33 33 - - - 59036 RMVar_ID_59036 Human_SNP_ID_704890074 m1A Human chr22 + 42686892 42686892 42686892 GCCCCTCACATTCAGTCTCAGCTGCGTGTCTCATCTGCTCATCCTCCCATCTCTCCAGCCACTTG GCCCCTCACATTCAGTCTCAGCTGCGTGTCTCGTCTGCTCATCCTCCCATCTCTCCAGCCACTTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:42686861..42687012 26863196 MeRIP-seq:(Medium) rs12628410 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6890,GWAS_ID_6891,GWAS_ID_6892,GWAS_ID_6893 59037 RMVar_ID_59037 Human_SNP_ID_704891724 m1A Human chr22 + 42692484 42692484 42692484 GGCTGGGTCTCCCCCAGCCCTGCCACTTTCCTACCAACAGCCTCCTCTCCTCTCTGGGAATCTTG GGCTGGGTCTCCCCCAGCCCTGCCACTTTCCTCCCAACAGCCTCCTCTCCTCTCTGGGAATCTTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42692348..42692683 26863196 MeRIP-seq:(Medium) rs1355203972 Functional Loss SNV dbSNP153 33..33 33 - - - 59038 RMVar_ID_59038 Human_SNP_ID_704891876 m1A Human chr22 - 42692826 42692826 42692826 CCTGATGGGGCACTGGGCCGCCCTTCCCGGGGAGGCAAGATTGAGGGCCCGGGAGAGGGAGGCCC CCTGATGGGGCACTGGGCCGCCCTTCCCGGGGTGGCAAGATTGAGGGCCCGGGAGAGGGAGGCCC T A A4GALT Ensembl:ENSG00000128274 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42692779..42692893 26863196 MeRIP-seq:(Medium) rs1259991693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582233 59039 RMVar_ID_59039 Human_SNP_ID_704891954 m1A Human chr22 - 42692967 42692967 42692967 ACAAGAAGAGCCAGGGCACGCGGTTCGAGGCCACGTCCAGGGCACTGCTGGCCCAGCTGCATGCC ACAAGAAGAGCCAGGGCACGCGGTTCGAGGCCGCGTCCAGGGCACTGCTGGCCCAGCTGCATGCC T C A4GALT Ensembl:ENSG00000128274 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:42692918..42693019 32194978 MeRIP-seq:(Medium) rs111767731 Functional Loss SNV dbSNP153 33..33 33 - - - 59040 RMVar_ID_59040 Human_SNP_ID_704891988 m1A Human chr22 + 42693032 42693032 42693032 TCCACACGTGGACAGCATAGGTGGCACTGAGCAGCCGCGGCAGCTCCTCGGGGTTGATGTCCTCA TCCACACGTGGACAGCATAGGTGGCACTGAGCGGCCGCGGCAGCTCCTCGGGGTTGATGTCCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42692983..42693051 26863196 MeRIP-seq:(Medium) rs145624551 Functional Loss SNV dbSNP153 33..33 33 - - - 59041 RMVar_ID_59041 Human_SNP_ID_704892063 m1A Human chr22 + 42693168 42693166 42693169 GGCGCGGCTCTCGGCCAGGCTGCGGATGGAACACCACTTCTTGAAGACCCGCGTGAGCAGCTGCG GGCGCGGCTCTCGGCCAGGCTGCGGATGGAA___CACTTCTTGAAGACCCGCGTGAGCAGCTGCG ACAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:42693117..42693318 32194978 MeRIP-seq:(Medium) rs771529410 Functional Loss DEL dbSNP153 32..34 33 - - - 59042 RMVar_ID_59042 Human_SNP_ID_704892065 m1A Human chr22 + 42693168 42693168 42693168 GGCGCGGCTCTCGGCCAGGCTGCGGATGGAACACCACTTCTTGAAGACCCGCGTGAGCAGCTGCG GGCGCGGCTCTCGGCCAGGCTGCGGATGGAACCCCACTTCTTGAAGACCCGCGTGAGCAGCTGCG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:42693117..42693318 32194978 MeRIP-seq:(Medium) rs1226363953 Functional Loss SNV dbSNP153 33..33 33 - - - 59043 RMVar_ID_59043 Human_SNP_ID_704892349 m1A Human chr22 - 42693680 42693680 42693680 CTTCCTGGAGACTTCAGACCGGACCAACCCCAACTTCCTGTTCATGTGCTCGGTGGAGTCGGCCG CTTCCTGGAGACTTCAGACCGGACCAACCCCAGCTTCCTGTTCATGTGCTCGGTGGAGTCGGCCG T C A4GALT Ensembl:ENSG00000128274 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42693629..42693700 26863196 MeRIP-seq:(Medium) rs767419574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23951108,Human_RBP_ID_27495076 59044 RMVar_ID_59044 Human_SNP_ID_704892799 m1A Human chr22 + 42695072 42695072 42695072 CAGGCCACCTGGCTGGGGTCCCTGCTCTCACCACTGCACCGCCCTGCCTGGGAGAGGTGGCTAGC CAGGCCACCTGGCTGGGGTCCCTGCTCTCACCGCTGCACCGCCCTGCCTGGGAGAGGTGGCTAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42695033..42695137 26863196 MeRIP-seq:(Medium) rs894658842 Functional Loss SNV dbSNP153 33..33 33 - - - 59045 RMVar_ID_59045 Human_SNP_ID_704892918 m1A Human chr22 + 42695586 42695586 42695586 CGCCCTGGCTCAGCAGCCGACCTTCTTTGCCAACACGAACACGGCCCTTCCACACACTTGCAGCG CGCCCTGGCTCAGCAGCCGACCTTCTTTGCCAGCACGAACACGGCCCTTCCACACACTTGCAGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42695453..42695655 26863196 MeRIP-seq:(Medium) rs1287913326 Functional Loss SNV dbSNP153 33..33 33 - - - 59046 RMVar_ID_59046 Human_SNP_ID_704894748 m1A Human chr22 + 42701996 42701996 42701996 ACGGAACCTTCTGATGACCTCCTCAATCGACCAATGAATGTCTCATCCCCCTGATCAGTGTCTTC ACGGAACCTTCTGATGACCTCCTCAATCGACCCATGAATGTCTCATCCCCCTGATCAGTGTCTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42701984..42702130 26863196 MeRIP-seq:(Medium) rs1156601161 Functional Loss SNV dbSNP153 33..33 33 - - - 59047 RMVar_ID_59047 Human_SNP_ID_704900374 m1A Human chr22 + 42720827 42720821 42720827 ACCTCTAGCTCCAGCGGCGGCGGGCGGCGGACAGCGGGGCCCCGGCGGGCGGGCGGCGCGGCGGC ACCTCTAGCTCCAGCGGCGGCGGGCGG______GCGGGGCCCCGGCGGGCGGGCGGCGCGGCGGC GCGGACA G lnc-SERHL2-3 RNACentral:URS00008B58C2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:42720717..42720875;chr22:42720702..42720846;chr22:42720644..42720852 26863196 MeRIP-seq:(Medium) rs1290680201 Functional Loss DEL dbSNP153 28..33 33 - - - 59048 RMVar_ID_59048 Human_SNP_ID_704938903 m1A Human chr22 + 42857205 42857205 42857205 GGTCCCCCATCGTCAGCTGTGAGCCGCGGCGCAGCTGGCCCAGCCAACCGGTAAGAGTCGACGAA GGTCCCCCATCGTCAGCTGTGAGCCGCGGCGCCGCTGGCCCAGCCAACCGGTAAGAGTCGACGAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42857155..42857229 26863196 MeRIP-seq:(Medium) rs1001945739 Functional Loss SNV dbSNP153 33..33 33 - - - 59049 RMVar_ID_59049 Human_SNP_ID_704943192 m1A Human chr22 - 42871452 42871452 42871452 CTCTTTGTCTTGCAGGGGATGAGCTGACCAAGATGGAGGACGAGGATGAGCAGGGCTGGTGCAAG CTCTTTGTCTTGCAGGGGATGAGCTGACCAAGTTGGAGGACGAGGATGAGCAGGGCTGGTGCAAG T A PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:42871317..42871497;chr22:42871276..42876350;chr22:42871301..42876272 26863196 MeRIP-seq:(Medium) rs1395534817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7089295,Human_RBP_ID_9392457,Human_RBP_ID_22454511,Human_RBP_ID_25680857,Human_RBP_ID_27039699,Human_RBP_ID_27495099 Human_Splice_Rec_2173070,Human_Splice_Rec_2173090,Human_Splice_Rec_2173108,Human_Splice_Rec_2173128,Human_Splice_Rec_2173148 59050 RMVar_ID_59050 Human_SNP_ID_704944406 m1A Human chr22 + 42876199 42876199 42876199 GCCCCTCATAGTCATACAGGGCCCGGACTCGCACTTCCGTCCCCGAGGTGGCGTCGTCGTCGAAT GCCCCTCATAGTCATACAGGGCCCGGACTCGCCCTTCCGTCCCCGAGGTGGCGTCGTCGTCGAAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42876103..42876374 26863196 MeRIP-seq:(Medium) rs768766374 Functional Loss SNV dbSNP153 33..33 33 - - - 59051 RMVar_ID_59051 Human_SNP_ID_704944407 m1A Human chr22 + 42876199 42876199 42876199 GCCCCTCATAGTCATACAGGGCCCGGACTCGCACTTCCGTCCCCGAGGTGGCGTCGTCGTCGAAT GCCCCTCATAGTCATACAGGGCCCGGACTCGCGCTTCCGTCCCCGAGGTGGCGTCGTCGTCGAAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42876103..42876374 26863196 MeRIP-seq:(Medium) rs768766374 Functional Loss SNV dbSNP153 33..33 33 - - - 59052 RMVar_ID_59052 Human_SNP_ID_704944627 m1A Human chr22 - 42876858 42876858 42876858 AAAGTTGGTGAACAAATGCTTCCTCTGCTCCCACCGCGCTCACTCTGTCTCTCTTCCTCTCTCTC AAAGTTGGTGAACAAATGCTTCCTCTGCTCCCGCCGCGCTCACTCTGTCTCTCTTCCTCTCTCTC T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:42876852..42877025 26863196 MeRIP-seq:(Medium) rs1409885554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19112309 RMVar_hsa_circ_103952,RMVar_hsa_circ_328712,RMVar_hsa_circ_366692,RMVar_hsa_circ_214833,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_42926,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214832 59053 RMVar_ID_59053 Human_SNP_ID_704945270 m1A Human chr22 - 42879120 42879118 42879121 GAATCGAACCCTCAGCCGGAGAGAGAAGAAGAAGGCCACTGACGGCGTCACCCTGACGGGCATCA GAATCGAACCCTCAGCCGGAGAGAGAAGAAG___GCCACTGACGGCGTCACCCTGACGGGCATCA CCTT C PACSIN2 Ensembl:ENSG00000100266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42879007..42879179 26863196 MeRIP-seq:(Medium) rs765787751 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9392462,Human_RBP_ID_19112310,Human_RBP_ID_22455060,Human_RBP_ID_25680670 Human_Splice_Rec_2173066,Human_Splice_Rec_2173067,Human_Splice_Rec_2173084,Human_Splice_Rec_2173085,Human_Splice_Rec_2173104,Human_Splice_Rec_2173105,Human_Splice_Rec_2173122,Human_Splice_Rec_2173123,Human_Splice_Rec_2173142,Human_Splice_Rec_2173143,Human_Splice_Rec_2173162,Human_Splice_Rec_2173163 RMVar_hsa_circ_103952,RMVar_hsa_circ_328712,RMVar_hsa_circ_366692,RMVar_hsa_circ_214833,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214832,RMVar_hsa_circ_266424 59054 RMVar_ID_59054 Human_SNP_ID_704945271 m1A Human chr22 - 42879120 42879120 42879120 GAATCGAACCCTCAGCCGGAGAGAGAAGAAGAAGGCCACTGACGGCGTCACCCTGACGGGCATCA GAATCGAACCCTCAGCCGGAGAGAGAAGAAGACGGCCACTGACGGCGTCACCCTGACGGGCATCA T G PACSIN2 Ensembl:ENSG00000100266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42879007..42879179 26863196 MeRIP-seq:(Medium) rs759434680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392462,Human_RBP_ID_19112310,Human_RBP_ID_22455060,Human_RBP_ID_25680670 Human_Splice_Rec_2173066,Human_Splice_Rec_2173067,Human_Splice_Rec_2173084,Human_Splice_Rec_2173085,Human_Splice_Rec_2173104,Human_Splice_Rec_2173105,Human_Splice_Rec_2173122,Human_Splice_Rec_2173123,Human_Splice_Rec_2173142,Human_Splice_Rec_2173143,Human_Splice_Rec_2173162,Human_Splice_Rec_2173163 RMVar_hsa_circ_103952,RMVar_hsa_circ_328712,RMVar_hsa_circ_366692,RMVar_hsa_circ_214833,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214832,RMVar_hsa_circ_266424 59055 RMVar_ID_59055 Human_SNP_ID_704949178 m1A Human chr22 + 42893604 42893604 42893604 GCCATCGTCGATCCGCTTCACAGTCCGCTTGTAGTTCCCGACCTAGGAGAGAGAACCAGCTGGGA GCCATCGTCGATCCGCTTCACAGTCCGCTTGTGGTTCCCGACCTAGGAGAGAGAACCAGCTGGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42888774..42909444 26863196 MeRIP-seq:(Medium) rs1322329319 Functional Loss SNV dbSNP153 33..33 33 - - - 59056 RMVar_ID_59056 Human_SNP_ID_704953819 m1A Human chr22 + 42912003 42912003 42912003 ACACTATTGGCCTGGCCACTTCATTCACTGGAAGAAAGCAGGTGCATTACCTCCCAGAAGCTGTC ACACTATTGGCCTGGCCACTTCATTCACTGGATGAAAGCAGGTGCATTACCTCCCAGAAGCTGTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42912001..42912050 26863196 MeRIP-seq:(Medium) rs375975538 Functional Loss SNV dbSNP153 33..33 33 - - - 59057 RMVar_ID_59057 Human_SNP_ID_704981213 m1A Human chr22 - 43014537 43014537 43014537 GACGTGCAGAGGTTAGGCGAGGGTGCCGGAGCAACGCTGGAGGGAAGGCGTGGCTGGGACGCGCC GACGTGCAGAGGTTAGGCGAGGGTGCCGGAGCTACGCTGGAGGGAAGGCGTGGCTGGGACGCGCC T A PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:43014535..43014689 26863196 MeRIP-seq:(Medium) rs1196869733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676807,Human_RBP_ID_5149564,Human_RBP_ID_8207384,Human_RBP_ID_14517088,Human_RBP_ID_23285830 RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 59058 RMVar_ID_59058 Human_SNP_ID_704981388 m1A Human chr22 - 43015092 43015092 43015092 GGGCTGGGCAGTGCTGCCGGAGCAAAAGCGGTAGCGGGAGCCCGGCCGGAGCTGGGTCTGGAGAC GGGCTGGGCAGTGCTGCCGGAGCAAAAGCGGTGGCGGGAGCCCGGCCGGAGCTGGGTCTGGAGAC T C PACSIN2 Ensembl:ENSG00000100266 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr22:43014959..43015175;chr22:43014835..43015150;chr22:43014863..43015150;chr22:43014801..43015150;chr22:43014745..43015150 26863196 MeRIP-seq:(Medium) rs1485083612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708728,Human_RBP_ID_18423662,Human_RBP_ID_23015520,Human_RBP_ID_23119875 Human_Splice_Rec_2173071,Human_Splice_Rec_2173167,Human_Splice_Rec_2173187 RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 59059 RMVar_ID_59059 Human_SNP_ID_704998453 m1A Human chr22 - 43075581 43075581 43075581 TCTAATATTTTGATCTCTTCCAGGATTATGGCAGGGAAAGTAAAATGGGTCACTGATATCGAGAA TCTAATATTTTGATCTCTTCCAGGATTATGGCGGGGAAAGTAAAATGGGTCACTGATATCGAGAA T C TTLL1 Ensembl:ENSG00000100271 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43075532..43075642 26863196 MeRIP-seq:(Medium) rs1189588536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2173202,Human_Splice_Rec_2173222,Human_Splice_Rec_2173244 RMVar_hsa_circ_304406,RMVar_hsa_circ_278619,RMVar_hsa_circ_214847,RMVar_hsa_circ_282934,RMVar_hsa_circ_214854,RMVar_hsa_circ_214856,RMVar_hsa_circ_20757,RMVar_hsa_circ_214857,RMVar_hsa_circ_2914,RMVar_hsa_circ_214858,RMVar_hsa_circ_298029,RMVar_hsa_circ_354862 59060 RMVar_ID_59060 Human_SNP_ID_705002595 m1A Human chr22 + 43089374 43089374 43089374 CGCCCCGCCTCCAGCCCCTCTCCGGCGCTCGCAGGAGTACGCAGCCGACTGCCAGGCGCACCGGC CGCCCCGCCTCCAGCCCCTCTCCGGCGCTCGCGGGAGTACGCAGCCGACTGCCAGGCGCACCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43089250..43089402 26863196 MeRIP-seq:(Medium) rs1228013069 Functional Loss SNV dbSNP153 33..33 33 - - - 59061 RMVar_ID_59061 Human_SNP_ID_705015241 m1A Human chr22 - 43133098 43133098 43133098 CATGCAGGCCTGGAAGTCCTACAGCGCCGTGGATGTGCTGCAGACCCTCGAACATGTGGACCTGG CATGCAGGCCTGGAAGTCCTACAGCGCCGTGGGTGTGCTGCAGACCCTCGAACATGTGGACCTGG T C MCAT Ensembl:ENSG00000100294 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:43133001..43133101 26863410 MeRIP-seq:(Medium) rs1430056236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7089559 59062 RMVar_ID_59062 Human_SNP_ID_705016458 m1A Human chr22 + 43137206 43137206 43137206 CCGGGCTTCCAAACAGGCGAAGTTGAACTTGGACTGAGGCTGGCCGAGGACAGACAGCATCCCAC CCGGGCTTCCAAACAGGCGAAGTTGAACTTGGGCTGAGGCTGGCCGAGGACAGACAGCATCCCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:43137092..43140873 32194978 MeRIP-seq:(Medium) rs1321463598 Functional Loss SNV dbSNP153 33..33 33 - - - 59063 RMVar_ID_59063 Human_SNP_ID_705018212 m1A Human chr22 - 43143239 43143239 43143239 GGTGCCTCCGCCGGGCGCCCAGGGTGTAGCGGAGCTGCTGCGAGATGCGACCGGGGCGGAGGAGG GGTGCCTCCGCCGGGCGCCCAGGGTGTAGCGGGGCTGCTGCGAGATGCGACCGGGGCGGAGGAGG T C MCAT Ensembl:ENSG00000100294 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:43143189..43143328 26863196 MeRIP-seq:(Medium) rs557699968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708293 59064 RMVar_ID_59064 Human_SNP_ID_705018251 m1A Human chr22 - 43143331 43143322 43143331 GGCAGGTGTCCGACCATGAGCGTCCGGGTCGCACGGGTAGCGTGGGTCAGGGGCTTGGGCGCCAG GGCAGGTGTCCGACCATGAGCGTCCGGGTCGC_________GTGGGTCAGGGGCTTGGGCGCCAG CGCTACCCGT C MCAT Ensembl:ENSG00000100294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:43142951..43143400;chr22:43142976..43143400 26863196 MeRIP-seq:(Medium) rs1327487385 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4703283,Human_RBP_ID_17987964 59065 RMVar_ID_59065 Human_SNP_ID_705018263 m1A Human chr22 + 43143335 43143335 43143335 CGCCCAAGCCCCTGACCCACGCTACCCGTGCGACCCGGACGCTCATGGTCGGACACCTGCCCGCG CGCCCAAGCCCCTGACCCACGCTACCCGTGCGGCCCGGACGCTCATGGTCGGACACCTGCCCGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:43143141..43143340 26863196 MeRIP-seq:(Medium) rs1157267844 Functional Loss SNV dbSNP153 33..33 33 - - - 59066 RMVar_ID_59066 Human_SNP_ID_705022876 m1A Human chr22 - 43159251 43159251 43159251 GGGCGCCAGCGTGAAGCCCATGGCGGGCACCCAGGGCGGGGCCATGGCTGCTGCAGCTGCTGTTC GGGCGCCAGCGTGAAGCCCATGGCGGGCACCCGGGGCGGGGCCATGGCTGCTGCAGCTGCTGTTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:43159201..43159275 26863196 MeRIP-seq:(Medium) rs753849621 Functional Loss SNV dbSNP153 33..33 33 - - - 59067 RMVar_ID_59067 Human_SNP_ID_705023971 m1A Human chr22 + 43162900 43162900 43162900 GAGCCCGCTGGCCGCCCGCCTGCTCTACCCCTACCTGGCCTGGCTGGCCTTCACGACCACACTCA GAGCCCGCTGGCCGCCCGCCTGCTCTACCCCTGCCTGGCCTGGCTGGCCTTCACGACCACACTCA A G TSPO Ensembl:ENSG00000100300 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43162849..43163075 26863196 MeRIP-seq:(Medium) rs1190281290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582345,Human_RBP_ID_9333420,Human_RBP_ID_27495125 Human_Splice_Rec_2173302,Human_Splice_Rec_2173308,Human_Splice_Rec_2173320,Human_Splice_Rec_2173326 Human_miRNA_ID_2398754 RMVar_hsa_circ_81072,RMVar_hsa_circ_113825,RMVar_hsa_circ_119779,RMVar_hsa_circ_214860,RMVar_hsa_circ_214861,RMVar_hsa_circ_266146,RMVar_hsa_circ_214863 59068 RMVar_ID_59068 Human_SNP_ID_705025764 m1A Human chr22 - 43168061 43168061 43168061 GGTACCACCCCACCTTCTTCAACGACGTCTTCAGCACCTTGTTTCTGGACCAGCCCGGTGGCTGC GGTACCACCCCACCTTCTTCAACGACGTCTTCCGCACCTTGTTTCTGGACCAGCCCGGTGGCTGC T G TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:43167926..43168125 26863196 MeRIP-seq:(Medium) rs755704040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65197,Human_RBP_ID_14517239 Human_Splice_Rec_2173352,Human_Splice_Rec_2173356,Human_Splice_Rec_2173362 Human_miRNA_ID_448457,Human_miRNA_ID_452348,Human_miRNA_ID_2144246,Human_miRNA_ID_2145775,Human_miRNA_ID_2688278,Human_miRNA_ID_2698112,Human_miRNA_ID_2942905 RMVar_hsa_circ_99722,RMVar_hsa_circ_103428,RMVar_hsa_circ_120351,RMVar_hsa_circ_118428,RMVar_hsa_circ_103225,RMVar_hsa_circ_214866,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_214864,RMVar_hsa_circ_214865 59069 RMVar_ID_59069 Human_SNP_ID_705025770 m1A Human chr22 - 43168082 43168082 43168082 CCGACTGTGAGCGAGCCTGCAGGTACCACCCCACCTTCTTCAACGACGTCTTCAGCACCTTGTTT CCGACTGTGAGCGAGCCTGCAGGTACCACCCCTCCTTCTTCAACGACGTCTTCAGCACCTTGTTT T A TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43168033..43168098 26863196 MeRIP-seq:(Medium) rs745624185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3674614,Human_RBP_ID_7089597,Human_RBP_ID_8552241,Human_RBP_ID_14517241 Human_Splice_Rec_2173352,Human_Splice_Rec_2173356,Human_Splice_Rec_2173362 RMVar_hsa_circ_99722,RMVar_hsa_circ_103428,RMVar_hsa_circ_120351,RMVar_hsa_circ_118428,RMVar_hsa_circ_103225,RMVar_hsa_circ_214866,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_214864,RMVar_hsa_circ_214865 59070 RMVar_ID_59070 Human_SNP_ID_705025771 m1A Human chr22 - 43168082 43168082 43168082 CCGACTGTGAGCGAGCCTGCAGGTACCACCCCACCTTCTTCAACGACGTCTTCAGCACCTTGTTT CCGACTGTGAGCGAGCCTGCAGGTACCACCCCGCCTTCTTCAACGACGTCTTCAGCACCTTGTTT T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43168033..43168098 26863196 MeRIP-seq:(Medium) rs745624185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3674614,Human_RBP_ID_7089597,Human_RBP_ID_8552241,Human_RBP_ID_14517241 Human_Splice_Rec_2173352,Human_Splice_Rec_2173356,Human_Splice_Rec_2173362 RMVar_hsa_circ_99722,RMVar_hsa_circ_103428,RMVar_hsa_circ_120351,RMVar_hsa_circ_118428,RMVar_hsa_circ_103225,RMVar_hsa_circ_214866,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_214864,RMVar_hsa_circ_214865 59071 RMVar_ID_59071 Human_SNP_ID_705026056 m1A Human chr22 + 43168851 43168850 43168851 TGGCCCGGGATGAGGGGTAGTCGCAGAGGCCCAGGGGTGGTGGCTTGGCACAGGCCACCTGGAAC TGGCCCGGGATGAGGGGTAGTCGCAGAGGCCC_GGGGTGGTGGCTTGGCACAGGCCACCTGGAAC CA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:43168801..43168875 26863196 MeRIP-seq:(Medium) rs1569483012 Functional Loss DEL dbSNP153 33..33 33 - - - 59072 RMVar_ID_59072 Human_SNP_ID_705027280 m1A Human chr22 - 43172499 43172499 43172499 TCCCGTGTTGTTCCTTCGAGAAGACGTGGGAAAGGTCAAGTTCGACATCCGCTACATCGTGCTGC TCCCGTGTTGTTCCTTCGAGAAGACGTGGGAAGGGTCAAGTTCGACATCCGCTACATCGTGCTGC T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr22:43172448..43172602;chr22:43172401..43172598 26863196 MeRIP-seq:(Medium) rs201450134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9127258,Human_RBP_ID_26345511 Human_Splice_Rec_2173344,Human_Splice_Rec_2173345 RMVar_hsa_circ_120351,RMVar_hsa_circ_118428,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_214866,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_63976 59073 RMVar_ID_59073 Human_SNP_ID_705027296 m1A Human chr22 + 43172524 43172524 43172524 CTTGACCTTTCCCACGTCTTCTCGAAGGAACAACACGGGACTTTCGATGTACTTGGACACAACCT CTTGACCTTTCCCACGTCTTCTCGAAGGAACACCACGGGACTTTCGATGTACTTGGACACAACCT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:43172476..43172575 26863196 MeRIP-seq:(Medium) rs1569483959 Functional Loss SNV dbSNP153 33..33 33 - - - 59074 RMVar_ID_59074 Human_SNP_ID_705027653 m1A Human chr22 - 43173668 43173667 43173668 CCAGGAGCCCCAGGGCTCAGGGCCCTGGCTGGACAGTGAGAGGTGGGGCTAAGGGGACCGAGCAT CCAGGAGCCCCAGGGCTCAGGGCCCTGGCTGG_CAGTGAGAGGTGGGGCTAAGGGGACCGAGCAT GT G TTLL12 Ensembl:ENSG00000100304 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43173666..43173850 26863196 MeRIP-seq:(Medium) rs59626434 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_63976 59075 RMVar_ID_59075 Human_SNP_ID_705027902 m1A Human chr22 + 43174176 43174176 43174176 CGGACACAGACGCTGGGCCGGGGAAAAGGGCCATGGAGCACACCGATGCCGTGTCTGGGACTTAC CGGACACAGACGCTGGGCCGGGGAAAAGGGCCGTGGAGCACACCGATGCCGTGTCTGGGACTTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43174172..43174419 26863196 MeRIP-seq:(Medium) rs1395891688 Functional Loss SNV dbSNP153 33..33 33 - - - 59076 RMVar_ID_59076 Human_SNP_ID_705028139 m1A Human chr22 + 43174580 43174580 43174580 CACTCTGGGTGAGGGTGAAGCGCGGGTGGGTGAGGCTGCTGGCCACCTGCTGCACGTCCGTGTAG CACTCTGGGTGAGGGTGAAGCGCGGGTGGGTGGGGCTGCTGGCCACCTGCTGCACGTCCGTGTAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:43174368..43175317 32194978 MeRIP-seq:(Medium) rs1021385531 Functional Loss SNV dbSNP153 33..33 33 - - - 59077 RMVar_ID_59077 Human_SNP_ID_705028159 m1A Human chr22 - 43174617 43174617 43174617 AGCCGGGATCACCCAGCTCGGGCTCTCCCCACAGGGTCTACACGGACGTGCAGCAGGTGGCCAGC AGCCGGGATCACCCAGCTCGGGCTCTCCCCACGGGGTCTACACGGACGTGCAGCAGGTGGCCAGC T C TTLL12 Ensembl:ENSG00000100304 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43174501..43174625 26863196 MeRIP-seq:(Medium) rs1424235098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19113643,Human_RBP_ID_22550833,Human_RBP_ID_22674435 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_87082,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_63976,RMVar_hsa_circ_214871,RMVar_hsa_circ_292542 59078 RMVar_ID_59078 Human_SNP_ID_705028881 m1A Human chr22 + 43176368 43176368 43176368 GGGGGTGCACCACGGGGTTGATGTCAAGTGGCAGCTTCTCCTTGTTTTCCTCCAGAATGGCCTAA GGGGGTGCACCACGGGGTTGATGTCAAGTGGCGGCTTCTCCTTGTTTTCCTCCAGAATGGCCTAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:43176230..43176400 26863196 MeRIP-seq:(Medium) rs1047784145 Functional Loss SNV dbSNP153 33..33 33 - - - 59079 RMVar_ID_59079 Human_SNP_ID_705028886 m1A Human chr22 - 43176380 43176380 43176380 GTGTGTTTCCTTTTAGGCCATTCTGGAGGAAAACAAGGAGAAGCTGCCACTTGACATCAACCCCG GTGTGTTTCCTTTTAGGCCATTCTGGAGGAAAGCAAGGAGAAGCTGCCACTTGACATCAACCCCG T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:43176351..43176400 26863196 MeRIP-seq:(Medium) rs1397392837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387448,Human_RBP_ID_26345512 Human_Splice_Rec_2173336,Human_Splice_Rec_2173337 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_87082,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_63976,RMVar_hsa_circ_214871,RMVar_hsa_circ_292542,RMVar_hsa_circ_38231 59080 RMVar_ID_59080 Human_SNP_ID_705029984 m1A Human chr22 - 43179669 43179669 43179669 AGTGCATGCTGCTGCCCTGGGCCCCCACCGACATGCTGGACCTCAGCTCTTGCACACCCGAGCCG AGTGCATGCTGCTGCCCTGGGCCCCCACCGACGTGCTGGACCTCAGCTCTTGCACACCCGAGCCG T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43179567..43180029 26863196 MeRIP-seq:(Medium) rs1403458824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8864735,Human_RBP_ID_18791136 Human_Splice_Rec_2173334,Human_Splice_Rec_2173335 Human_miRNA_ID_2439199,Human_miRNA_ID_2442633 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_51571,RMVar_hsa_circ_38231 59081 RMVar_ID_59081 Human_SNP_ID_705031232 m1A Human chr22 - 43183031 43183031 43183031 GCAGCAGCCCAACCCGGGGAACGAGCTGTGCTACAAGGTCATCGTGACCAGGGAGAGCGGGCTCC GCAGCAGCCCAACCCGGGGAACGAGCTGTGCTGCAAGGTCATCGTGACCAGGGAGAGCGGGCTCC T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:43180903..43183042 26863410 MeRIP-seq:(Medium) rs1228047435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4703436,Human_RBP_ID_5389484,Human_RBP_ID_26770996 Human_Splice_Rec_2173329 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_51571,RMVar_hsa_circ_38231 59082 RMVar_ID_59082 Human_SNP_ID_705032698 m1A Human chr22 - 43187032 43187032 43187032 GGCCGAGCGGGGTCCCGAGCGCCGGCCTGCGGAGCGTAGCAGCCCGGGCCAGACGCCGGAGGAGG GGCCGAGCGGGGTCCCGAGCGCCGGCCTGCGGGGCGTAGCAGCCCGGGCCAGACGCCGGAGGAGG T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:43186933..43187133 26863410 MeRIP-seq:(Medium) rs1384080253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245956,Human_RBP_ID_4703443,Human_RBP_ID_19008185 RMVar_hsa_circ_120351,RMVar_hsa_circ_214870 59083 RMVar_ID_59083 Human_SNP_ID_705032726 m1A Human chr22 + 43187079 43187079 43187079 TCGGGACCCCGCTCGGCCTCCATGGCGCCAGCACCCGCGCCGACTCCAGCGCCGCCACCGCCGCC TCGGGACCCCGCTCGGCCTCCATGGCGCCAGCCCCCGCGCCGACTCCAGCGCCGCCACCGCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr22:43186837..43187150;chr22:43187033..43187133;chr22:43182976..43187150;chr22:43186826..43187150;chr22:43186901..43187100 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs549625874 Functional Loss SNV dbSNP153 33..33 33 - - - 59084 RMVar_ID_59084 Human_SNP_ID_705032782 m1A Human chr22 - 43187134 43187134 43187134 CGGGGCGGGGCAGGGGGCGGAGGCGGGAGGGCAGGGCCGACGGACGGCGGGCGGCGGCGGCGGTG CGGGGCGGGGCAGGGGGCGGAGGCGGGAGGGCGGGGCCGACGGACGGCGGGCGGCGGCGGCGGTG T C TTLL12 Ensembl:ENSG00000100304 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr22:43187033..43187133 26863410 MeRIP-seq:(Medium) rs1301982443 Functional Loss SNV dbSNP153 33..33 33 - - - 59085 RMVar_ID_59085 Human_SNP_ID_705118766 m1A Human chr22 + 43495281 43495278 43495281 TGGAGGTGGTGATGGAGGTGGTGGTGGTGGTGATGGAGGTGGTGATGGAGGTGATGGTGGTGATG TGGAGGTGGTGATGGAGGTGGTGGTGGTGG___TGGAGGTGGTGATGGAGGTGATGGTGGTGATG GTGA G MPPED1 Ensembl:ENSG00000186732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43495268..43495336 26863196 MeRIP-seq:(Medium) rs1346023062 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_11765,RMVar_hsa_circ_43993,RMVar_hsa_circ_338681,RMVar_hsa_circ_323053,RMVar_hsa_circ_214882 59086 RMVar_ID_59086 Human_SNP_ID_705118768 m1A Human chr22 + 43495281 43495281 43495281 TGGAGGTGGTGATGGAGGTGGTGGTGGTGGTGATGGAGGTGGTGATGGAGGTGATGGTGGTGATG TGGAGGTGGTGATGGAGGTGGTGGTGGTGGTGGTGGAGGTGGTGATGGAGGTGATGGTGGTGATG A G MPPED1 Ensembl:ENSG00000186732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43495268..43495336 26863196 MeRIP-seq:(Medium) rs1279145513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11765,RMVar_hsa_circ_43993,RMVar_hsa_circ_338681,RMVar_hsa_circ_323053,RMVar_hsa_circ_214882 59087 RMVar_ID_59087 Human_SNP_ID_705121137 m1A Human chr22 + 43499704 43499523 43499704 GGGTGATGGTGGTGATGGTGGTGGTGGAGGTGATGATGGTGGTGGTGATGGAGGTGGTGATGGGG _________________________________TGATGGTGGTGGTGATGGAGGTGGTGATGGGG GTGATGGAGGTGGTGGTGATGGTGGGTGGTGGTGGAGGTGGTGGTGGTGGTAGTGGAGGTGGTGGTGGTAGTGGAGGTGGTGGTGGTGGTGATGGTGGTGGTGATGATGGTGGAGGTGGTGGTGGTGGTGATGGGGGTGGCGGTGATGGGGGTGATGGTGGTGATGGTGGTGGTGGAGGTGA G MPPED1 Ensembl:ENSG00000186732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43499671..43499747 26863196 MeRIP-seq:(Medium) rs1569091099 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_43993,RMVar_hsa_circ_338681,RMVar_hsa_circ_323053,RMVar_hsa_circ_214882,RMVar_hsa_circ_291322,RMVar_hsa_circ_214884 59088 RMVar_ID_59088 Human_SNP_ID_705121278 m1A Human chr22 - 43499684 43499684 43499684 CCACCACCATCATCACCTCCACCACCACCATCACCACCATCACCCCCATCACCGCCACCCCCATC CCACCACCATCATCACCTCCACCACCACCATCGCCACCATCACCCCCATCACCGCCACCCCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:43499666..43499750 26863196 MeRIP-seq:(Medium) rs1419490449 Functional Loss SNV dbSNP153 33..33 33 - - - 59089 RMVar_ID_59089 Human_SNP_ID_705121282 m1A Human chr22 - 43499687 43499687 43499687 TCACCACCACCATCATCACCTCCACCACCACCATCACCACCATCACCCCCATCACCGCCACCCCC TCACCACCACCATCATCACCTCCACCACCACCTTCACCACCATCACCCCCATCACCGCCACCCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:43499666..43499757 26863196 MeRIP-seq:(Medium) rs1187501122 Functional Loss SNV dbSNP153 33..33 33 - - - 59090 RMVar_ID_59090 Human_SNP_ID_705121295 m1A Human chr22 + 43499704 43499701 43499704 GGGTGATGGTGGTGATGGTGGTGGTGGAGGTGATGATGGTGGTGGTGATGGAGGTGGTGATGGGG GGGTGATGGTGGTGATGGTGGTGGTGGAGG___TGATGGTGGTGGTGATGGAGGTGGTGATGGGG GTGA G MPPED1 Ensembl:ENSG00000186732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43499671..43499747 26863196 MeRIP-seq:(Medium) rs755194663 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_43993,RMVar_hsa_circ_338681,RMVar_hsa_circ_323053,RMVar_hsa_circ_214882,RMVar_hsa_circ_291322,RMVar_hsa_circ_214884 59091 RMVar_ID_59091 Human_SNP_ID_705121296 m1A Human chr22 + 43499704 43499704 43499704 GGGTGATGGTGGTGATGGTGGTGGTGGAGGTGATGATGGTGGTGGTGATGGAGGTGGTGATGGGG GGGTGATGGTGGTGATGGTGGTGGTGGAGGTGGTGATGGTGGTGGTGATGGAGGTGGTGATGGGG A G MPPED1 Ensembl:ENSG00000186732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43499671..43499747 26863196 MeRIP-seq:(Medium) rs866157127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43993,RMVar_hsa_circ_338681,RMVar_hsa_circ_323053,RMVar_hsa_circ_214882,RMVar_hsa_circ_291322,RMVar_hsa_circ_214884 59092 RMVar_ID_59092 Human_SNP_ID_705207012 m1A Human chr22 + 43835006 43835006 43835006 GCCCCCACCGCTGCCCTGAGCTTCCCGCACCCACACCGCGGCCCTGTGCTTCCCGCGCCCCCACC GCCCCCACCGCTGCCCTGAGCTTCCCGCACCCCCACCGCGGCCCTGTGCTTCCCGCGCCCCCACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:43834964..43835138;chr22:43834946..43835465 26863196 MeRIP-seq:(Medium) rs865856202 Functional Loss SNV dbSNP153 33..33 33 - - - 59093 RMVar_ID_59093 Human_SNP_ID_705211847 m1A Human chr22 + 43853093 43853089 43853093 ACATAACACACAGACCACACACACTCCTCCAAACACAGCACGCACACACACACCAGACACAGACC ACATAACACACAGACCACACACACTCCTC____CACAGCACGCACACACACACCAGACACAGACC CCAAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43853085..43853153 26863196 MeRIP-seq:(Medium) rs1317607148 Functional Loss DEL dbSNP153 30..33 33 - - - 59094 RMVar_ID_59094 Human_SNP_ID_705231538 m1A Human chr22 - 43923859 43923859 43923859 GGCGCGGGTTAGGATCTGGGTCGGGATCGGGAATCGGCTCGGGTCCTGATCCGCAGCAGCTCCGC GGCGCGGGTTAGGATCTGGGTCGGGATCGGGAGTCGGCTCGGGTCCTGATCCGCAGCAGCTCCGC T C lnc-PNPLA5-6,lnc-PNPLA5-6:2,lnc-PNPLA5-6:3 RNACentral:URS0000D57813,RNACentral:URS0000D5A66E,RNACentral:URS0000D5D7FA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:43923811..43923931 26863196 MeRIP-seq:(Medium) rs1044141868 Functional Loss SNV dbSNP153 33..33 33 - - - 59095 RMVar_ID_59095 Human_SNP_ID_705242351 m1A Human chr22 + 43963335 43963332 43963335 ATCAAGTGGACCTGATTTTGGAGGATTAGGAGAAGAAGCTGAATTTGTTGAAGTTGAGCCTGAAG ATCAAGTGGACCTGATTTTGGAGGATTAGG___AGAAGCTGAATTTGTTGAAGTTGAGCCTGAAG GAGA G SAMM50,PNPLA3 Ensembl:ENSG00000100347,Ensembl:ENSG00000100344 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43963237..43963350 26863196 MeRIP-seq:(Medium) rs1239217484 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1944213,Human_RBP_ID_4703496,Human_RBP_ID_7089788,Human_RBP_ID_9127278,Human_RBP_ID_9392480,Human_RBP_ID_14518023 Human_Splice_Rec_2173848,Human_Splice_Rec_2173849,Human_Splice_Rec_2173908,Human_Splice_Rec_2173909 RMVar_hsa_circ_214928,RMVar_hsa_circ_334038,RMVar_hsa_circ_364945,RMVar_hsa_circ_331821 59096 RMVar_ID_59096 Human_SNP_ID_705242353 m1A Human chr22 + 43963335 43963335 43963335 ATCAAGTGGACCTGATTTTGGAGGATTAGGAGAAGAAGCTGAATTTGTTGAAGTTGAGCCTGAAG ATCAAGTGGACCTGATTTTGGAGGATTAGGAGGAGAAGCTGAATTTGTTGAAGTTGAGCCTGAAG A G SAMM50,PNPLA3 Ensembl:ENSG00000100347,Ensembl:ENSG00000100344 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43963237..43963350 26863196 MeRIP-seq:(Medium) rs200348301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1944213,Human_RBP_ID_4703496,Human_RBP_ID_7089788,Human_RBP_ID_9127278,Human_RBP_ID_9392480,Human_RBP_ID_14518023 Human_Splice_Rec_2173848,Human_Splice_Rec_2173849,Human_Splice_Rec_2173908,Human_Splice_Rec_2173909 RMVar_hsa_circ_214928,RMVar_hsa_circ_334038,RMVar_hsa_circ_364945,RMVar_hsa_circ_331821 59097 RMVar_ID_59097 Human_SNP_ID_705249213 m1A Human chr22 + 43989161 43989161 43989161 AAGCGTACTGGGCCGGCGGCCTGCACCTCTACACCCCATTACCTTTCCGGCCAGGCCAGGGTGGC AAGCGTACTGGGCCGGCGGCCTGCACCTCTACCCCCCATTACCTTTCCGGCCAGGCCAGGGTGGC A C SAMM50 Ensembl:ENSG00000100347 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:43989080..43989181 32194978 MeRIP-seq:(Medium) rs1181488940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245997,Human_RBP_ID_17399587,Human_RBP_ID_17988067,Human_RBP_ID_18209646,Human_RBP_ID_22454516,Human_RBP_ID_27495159 Human_Splice_Rec_2173930,Human_Splice_Rec_2173931,Human_Splice_Rec_2173944,Human_Splice_Rec_2173945,Human_Splice_Rec_2173949 RMVar_hsa_circ_116390,RMVar_hsa_circ_23770,RMVar_hsa_circ_124038,RMVar_hsa_circ_352132,RMVar_hsa_circ_76226,RMVar_hsa_circ_214929,RMVar_hsa_circ_214930,RMVar_hsa_circ_19549,RMVar_hsa_circ_214932,RMVar_hsa_circ_320114 59098 RMVar_ID_59098 Human_SNP_ID_705258129 m1A Human chr22 + 44022474 44022474 44022474 GGCCACTGTGTCCTGTGCCCACGTTCTCCTTGACCACAAACTCCTGGAGGACAAAGCTCTGTGCC GGCCACTGTGTCCTGTGCCCACGTTCTCCTTGTCCACAAACTCCTGGAGGACAAAGCTCTGTGCC A T PARVB Ensembl:ENSG00000188677 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:44022423..44022536 26863196 MeRIP-seq:(Medium) rs953462696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16447 59099 RMVar_ID_59099 Human_SNP_ID_705263011 m1A Human chr22 + 44040351 44040351 44040351 TGGTAGACTGAATAGTAGTACCAAAAATGTCTATATTCCAATACCTGGAAACTGAGAATATGTTC TGGTAGACTGAATAGTAGTACCAAAAATGTCTGTATTCCAATACCTGGAAACTGAGAATATGTTC A G PARVB Ensembl:ENSG00000188677 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44040349..44040551 26863196 MeRIP-seq:(Medium) rs566502741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16447 59100 RMVar_ID_59100 Human_SNP_ID_705274267 m1A Human chr22 + 44083434 44083434 44083434 GCACTCCTTGCGGGGTCGGGGGGTGCAGGGAGATGAGCACAGTCCACAATCACATGATCGGGGAA GCACTCCTTGCGGGGTCGGGGGGTGCAGGGAGTTGAGCACAGTCCACAATCACATGATCGGGGAA A T PARVB Ensembl:ENSG00000188677 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:44083431..44083637 26863196 MeRIP-seq:(Medium) rs10427937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16447 59101 RMVar_ID_59101 Human_SNP_ID_705322816 m1A Human chr22 - 44254956 44254956 44254956 AGGATGAGTGAAAGGGGGACTGAGAATTGACCACTGGGTTTATTAACAGAGAGGTCTTTGGTGAC AGGATGAGTGAAAGGGGGACTGAGAATTGACCGCTGGGTTTATTAACAGAGAGGTCTTTGGTGAC T C SHISAL1 Ensembl:ENSG00000138944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44254953..44255080 26863196 MeRIP-seq:(Medium) rs1037730280 Functional Loss SNV dbSNP153 33..33 33 - - - 59102 RMVar_ID_59102 Human_SNP_ID_705327191 m1A Human chr22 + 44269645 44269644 44269645 ACCCACACAATATACACACACATGCCACAAACAACACACACACAATGTCACATAGACCCACACAA ACCCACACAATATACACACACATGCCACAAAC_ACACACACACAATGTCACATAGACCCACACAA CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44269642..44269772 26863196 MeRIP-seq:(Medium) rs1467407919 Functional Loss DEL dbSNP153 33..33 33 - - - 59103 RMVar_ID_59103 Human_SNP_ID_705327192 m1A Human chr22 + 44269645 44269645 44269645 ACCCACACAATATACACACACATGCCACAAACAACACACACACAATGTCACATAGACCCACACAA ACCCACACAATATACACACACATGCCACAAACCACACACACACAATGTCACATAGACCCACACAA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44269642..44269772 26863196 MeRIP-seq:(Medium) rs1053591212 Functional Loss SNV dbSNP153 33..33 33 - - - 59104 RMVar_ID_59104 Human_SNP_ID_705342109 m1A Human chr22 - 44323158 44323158 44323158 ATGCATGGATGGATGAATGGATGGATGGATGGATGAATGGGTGGATGGATGGATGGATGAACGGG ATGCATGGATGGATGAATGGATGGATGGATGGTTGAATGGGTGGATGGATGGATGGATGAACGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44323157..44323309 26863196 MeRIP-seq:(Medium) rs1004543256 Functional Loss SNV dbSNP153 33..33 33 - - - 59105 RMVar_ID_59105 Human_SNP_ID_705342389 m1A Human chr22 + 44323685 44323683 44323686 ATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCATCCCTTCATTCTCAGCAACCT ATCCATCCATCCATCCATCCATCCATCCATC___CCATCTATCATCCCTTCATTCTCAGCAACCT CCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44323683..44323780 26863196 MeRIP-seq:(Medium) rs1242565992 Functional Loss DEL dbSNP153 32..34 33 - - - 59106 RMVar_ID_59106 Human_SNP_ID_705344468 m1A Human chr22 - 44331146 44331146 44331146 CTCACCAAGGTCGGGGTCGCTGAACCTTGGAGAGGAAGGGGCTGGGTTCCGAAGAGAGCAGTTCG CTCACCAAGGTCGGGGTCGCTGAACCTTGGAGGGGAAGGGGCTGGGTTCCGAAGAGAGCAGTTCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44331143..44331255 26863196 MeRIP-seq:(Medium) rs1400157066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5424617,Human_RBP_ID_5446667,Human_RBP_ID_7089874,Human_RBP_ID_23955411 59107 RMVar_ID_59107 Human_SNP_ID_705344707 m1A Human chr22 - 44331931 44331888 44331931 GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGCGGGGCCCGGCGAGCATGAGCGCGGCGGC GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCG_________________________________ CCGCCGCCGCCGCCGCCGCGCTCATGCTCGCCGGGCCCCGCGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:44331901..44332056 26863196 MeRIP-seq:(Medium) rs1323738479 Functional Loss DEL dbSNP153 33..65 33 - - - 59108 RMVar_ID_59108 Human_SNP_ID_705344708 m1A Human chr22 - 44331931 44331891 44331931 GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGCGGGGCCCGGCGAGCATGAGCGCGGCGGC GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCG_________________________________ CCGCCGCCGCCGCCGCGCTCATGCTCGCCGGGCCCCGCGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:44331901..44332056 26863196 MeRIP-seq:(Medium) rs1310800808 Functional Loss DEL dbSNP153 33..65 33 - - - 59109 RMVar_ID_59109 Human_SNP_ID_705344719 m1A Human chr22 - 44331931 44331931 44331931 GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGCGGGGCCCGGCGAGCATGAGCGCGGCGGC GGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGCGGGGCCCGGCGAGCATGAGCGCGGCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:44331901..44332056 26863196 MeRIP-seq:(Medium) rs1357154620 Functional Loss SNV dbSNP153 33..33 33 - - - 59110 RMVar_ID_59110 Human_SNP_ID_705344734 m1A Human chr22 - 44331959 44331941 44331959 GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGC__________________GGCGGCGGCGAGCGC CGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44331874..44332003 26863196 MeRIP-seq:(Medium) rs1231194642 Functional Loss DEL dbSNP153 33..50 33 - - - 59111 RMVar_ID_59111 Human_SNP_ID_705344737 m1A Human chr22 - 44331959 44331950 44331959 GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGC_________GGCGGCGGCGGCGGCGGCGAGCGC CGCCGCCGCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44331874..44332003 26863196 MeRIP-seq:(Medium) rs1313592284 Functional Loss DEL dbSNP153 33..41 33 - - - 59112 RMVar_ID_59112 Human_SNP_ID_705344740 m1A Human chr22 - 44331959 44331953 44331959 GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGC______GGCGGCGGCGGCGGCGGCGGCGAGCGC CGCCGCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44331874..44332003 26863196 MeRIP-seq:(Medium) rs761428002 Functional Loss DEL dbSNP153 33..38 33 - - - 59113 RMVar_ID_59113 Human_SNP_ID_705344742 m1A Human chr22 - 44331959 44331956 44331959 GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGC___GGCGGCGGCGGCGGCGGCGGCGGCGAGCGC CGCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44331874..44332003 26863196 MeRIP-seq:(Medium) rs1194725416 Functional Loss DEL dbSNP153 33..35 33 - - - 59114 RMVar_ID_59114 Human_SNP_ID_705344744 m1A Human chr22 - 44331959 44331959 44331959 GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC GCGCGGAGCGAGCGCCAAAGAGTGAAGTGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44331874..44332003 26863196 MeRIP-seq:(Medium) rs1355660614 Functional Loss SNV dbSNP153 33..33 33 - - - 59115 RMVar_ID_59115 Human_SNP_ID_705344844 m1A Human chr22 - 44332199 44332199 44332199 GTAAAAAGAGAGAAAGTGAGAAGCCACCGCAAACAGCAGGAGGGGAGAGAGAAAGAGCCAGAGGG GTAAAAAGAGAGAAAGTGAGAAGCCACCGCAAGCAGCAGGAGGGGAGAGAGAAAGAGCCAGAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:44332149..44332241 26863196 MeRIP-seq:(Medium) rs1402007097 Functional Loss SNV dbSNP153 33..33 33 - - - 59116 RMVar_ID_59116 Human_SNP_ID_705387798 m1A Human chr22 - 44493731 44493731 44493731 GGAACAAGCCCTGGGATTGGACAAAAGGGCCCATGCTGCAGCCACTGACTGGGGGCAGAGCTCTG GGAACAAGCCCTGGGATTGGACAAAAGGGCCCGTGCTGCAGCCACTGACTGGGGGCAGAGCTCTG T C RTL6 Ensembl:ENSG00000188636 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:44493689..44493828 26863196 MeRIP-seq:(Medium) rs1055779230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7089915 59117 RMVar_ID_59117 Human_SNP_ID_705447197 m1A Human chr22 + 44702313 44702293 44702313 CGGCGGGGCGGCCGGCGCGGGACCCGAGACGGAGGCGCGGGGCCGGGGCGGGACCCCGCAGGACC CGGCGGGGCGGCC____________________GGCGCGGGGCCGGGGCGGGACCCCGCAGGACC CGGCGCGGGACCCGAGACGGA C PRR5-ARHGAP8,PRR5 Ensembl:ENSG00000248405,Ensembl:ENSG00000186654 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:44702265..44702579;chr22:44702227..44714611 26863196 MeRIP-seq:(Medium) rs1356635253 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_3676825,Human_RBP_ID_26789904 Human_Splice_Rec_2174451 59118 RMVar_ID_59118 Human_SNP_ID_705456576 m1A Human chr22 + 44732419 44732414 44732420 TGCAGGTGGGCACAGTGGGCAGAGGGTCGGGCATGGGGACCGTGGGGCAGTAATTGGGCTCAGGT TGCAGGTGGGCACAGTGGGCAGAGGGTC______GGGGACCGTGGGGCAGTAATTGGGCTCAGGT CGGGCAT C PRR5-ARHGAP8,PRR5 Ensembl:ENSG00000248405,Ensembl:ENSG00000186654 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:44732413..44732570 26863196 MeRIP-seq:(Medium) rs764198981 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_19112333,Human_RBP_ID_26789910 59119 RMVar_ID_59119 Human_SNP_ID_705458606 m1A Human chr22 + 44737041 44737041 44737041 CCCCGGCGCCCCACTCAGGGCCCTGCCCCAGCAGACTGTACCCCACGACCCAGCCCCCTGAGCAG CCCCGGCGCCCCACTCAGGGCCCTGCCCCAGCGGACTGTACCCCACGACCCAGCCCCCTGAGCAG A G PRR5-ARHGAP8,PRR5 Ensembl:ENSG00000248405,Ensembl:ENSG00000186654 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44736887..44737055 26863196 MeRIP-seq:(Medium) rs1433290983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4703851,Human_RBP_ID_27309858,Human_RBP_ID_27495298 59120 RMVar_ID_59120 Human_SNP_ID_705463620 m1A Human chr22 - 44752617 44752617 44752617 CTCCCGCCGCCGCCCGCCTTACCTGGCCACGGACCCCGCCGGCCCCCACCTGCGTGCCGGGTCTG CTCCCGCCGCCGCCCGCCTTACCTGGCCACGGCCCCCGCCGGCCCCCACCTGCGTGCCGGGTCTG T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:44752576..44752666 26863410 MeRIP-seq:(Medium) rs1333861498 Functional Loss SNV dbSNP153 33..33 33 - - - 59121 RMVar_ID_59121 Human_SNP_ID_705569977 m1A Human chr22 + 45080320 45080320 45080320 TCATCATCATCACCATCCTCATCACCATCACCATCATCATCACCATCATCACCATCATCATCATC TCATCATCATCACCATCCTCATCACCATCACCGTCATCATCACCATCATCACCATCATCATCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:45080274..45080362;chr22:45080240..45080347 26863196 MeRIP-seq:(Medium) rs1411789517 Functional Loss SNV dbSNP153 33..33 33 - - - 59122 RMVar_ID_59122 Human_SNP_ID_705569983 m1A Human chr22 - 45080327 45080327 45080327 TGATAATGATGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGAGGATGGTGATG TGATAATGATGATGATGATGGTGATGATGGTGGTGATGATGGTGATGGTGATGAGGATGGTGATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45080276..45080382 26863196 MeRIP-seq:(Medium) rs1392671531 Functional Loss SNV dbSNP153 33..33 33 - - - 59123 RMVar_ID_59123 Human_SNP_ID_705592064 m1A Human chr22 - 45162547 45162547 45162547 GACATGGGCTCTACCACGAGGGCCCACGACCAAGGTTTCATGCGCGTCCGTGTGAAGAGACCACC GACATGGGCTCTACCACGAGGGCCCACGACCAGGGTTTCATGCGCGTCCGTGTGAAGAGACCACC T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45162544..45162745 26863196 MeRIP-seq:(Medium) rs1345655491 Functional Loss SNV dbSNP153 33..33 33 - - - 59124 RMVar_ID_59124 Human_SNP_ID_705592432 m1A Human chr22 - 45163621 45163621 45163621 CATGGCCGAGGCCCGCGGTGTCCGCGTGTGGGAGCTGCAGGGCTGAGGAGAGGCCGCCCGCAACC CATGGCCGAGGCCCGCGGTGTCCGCGTGTGGGGGCTGCAGGGCTGAGGAGAGGCCGCCCGCAACC T C NUP50-DT Ensembl:ENSG00000226328 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45163571..45163742 26863196 MeRIP-seq:(Medium) rs571146534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7090147,Human_RBP_ID_18423667,Human_RBP_ID_22087221,Human_RBP_ID_23015523,Human_RBP_ID_23119877 Human_Splice_Rec_2174917,Human_Splice_Rec_2174927 59125 RMVar_ID_59125 Human_SNP_ID_705592446 m1A Human chr22 + 45163651 45163651 45163651 GCTCCCACACGCGGACACCGCGGGCCTCGGCCATGTCCACTGACCGACCTTCCTCGCCGGAACTC GCTCCCACACGCGGACACCGCGGGCCTCGGCCGTGTCCACTGACCGACCTTCCTCGCCGGAACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45163551..45163749 26863196 MeRIP-seq:(Medium) rs764299397 Functional Loss SNV dbSNP153 33..33 33 - - - 59126 RMVar_ID_59126 Human_SNP_ID_705592675 m1A Human chr22 - 45164072 45164072 45164072 GCTCCTCACGCTGTGTTCGGCAGGGAGGCGAGAGCGCCGGTTCAGCCAGAGACAGCTGGGGGAAC GCTCCTCACGCTGTGTTCGGCAGGGAGGCGAGGGCGCCGGTTCAGCCAGAGACAGCTGGGGGAAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45164021..45164154 26863196 MeRIP-seq:(Medium) rs1244417644 Functional Loss SNV dbSNP153 33..33 33 - - - 59127 RMVar_ID_59127 Human_SNP_ID_705604424 m1A Human chr22 - 45200037 45200037 45200037 TGCTACTCTGGTGACTTTGGCTGCTTGTTCCCAGGTGACCTCCTTCAGCACACCCCCCACCCCAG TGCTACTCTGGTGACTTTGGCTGCTTGTTCCCGGGTGACCTCCTTCAGCACACCCCCCACCCCAG T C KIAA0930 Ensembl:ENSG00000100364 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:45200026..45200176 32194978 MeRIP-seq:(Medium) rs1258572740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931743 RMVar_hsa_circ_111914,RMVar_hsa_circ_120856,RMVar_hsa_circ_122354,RMVar_hsa_circ_120499,RMVar_hsa_circ_104973,RMVar_hsa_circ_110938,RMVar_hsa_circ_97760,RMVar_hsa_circ_214962,RMVar_hsa_circ_214966,RMVar_hsa_circ_214967,RMVar_hsa_circ_214964,RMVar_hsa_circ_214965,RMVar_hsa_circ_214963,RMVar_hsa_circ_19533,RMVar_hsa_circ_214961,RMVar_hsa_circ_363532 59128 RMVar_ID_59128 Human_SNP_ID_705605695 m1A Human chr22 + 45203948 45203948 45203948 TGGTTTTGTCACTAGCCACCAGCTCCACACAGACCATCTCTCCTTCCCCTACGGTCATGTCGCTG TGGTTTTGTCACTAGCCACCAGCTCCACACAGGCCATCTCTCCTTCCCCTACGGTCATGTCGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45203897..45204028 26863196 MeRIP-seq:(Medium) rs1375594623 Functional Loss SNV dbSNP153 33..33 33 - - - 59129 RMVar_ID_59129 Human_SNP_ID_705607994 m1A Human chr22 + 45210745 45210745 45210745 ACCAGTCAGGCCTCCTCTTCATCCCTCCCAGAAAGCATTCCCTGCCTGCCCGAGTGTGGCTCTAG ACCAGTCAGGCCTCCTCTTCATCCCTCCCAGAGAGCATTCCCTGCCTGCCCGAGTGTGGCTCTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45210743..45210928 26863196 MeRIP-seq:(Medium) rs1381385342 Functional Loss SNV dbSNP153 33..33 33 - - - 59130 RMVar_ID_59130 Human_SNP_ID_705617763 m1A Human chr22 + 45240858 45240855 45240858 CTGTGCGCGTCGCCGTCGCCGCCGCCGCCGCCACCACCCGCCAAACACAGCACCGGCGAGCGCAC CTGTGCGCGTCGCCGTCGCCGCCGCCGCCG___CCACCCGCCAAACACAGCACCGGCGAGCGCAC GCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:45240788..45240901 26863196 MeRIP-seq:(Medium) rs1274856555 Functional Loss DEL dbSNP153 31..33 33 - - - 59131 RMVar_ID_59131 Human_SNP_ID_705638642 m1A Human chr22 - 45310010 45310010 45310010 GCGCAGGCACGCGGGCTAGAAGCGAGAGCGAGAGCCGGAGTCGGAGCCAGAGCGGACGCCACGCC GCGCAGGCACGCGGGCTAGAAGCGAGAGCGAGGGCCGGAGTCGGAGCCAGAGCGGACGCCACGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45309909..45310139 26863196 MeRIP-seq:(Medium) rs1485212540 Functional Loss SNV dbSNP153 33..33 33 - - - 59132 RMVar_ID_59132 Human_SNP_ID_705638651 m1A Human chr22 - 45310018 45310018 45310018 AGGGGACTGCGCAGGCACGCGGGCTAGAAGCGAGAGCGAGAGCCGGAGTCGGAGCCAGAGCGGAC AGGGGACTGCGCAGGCACGCGGGCTAGAAGCGGGAGCGAGAGCCGGAGTCGGAGCCAGAGCGGAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45309967..45310083 26863196 MeRIP-seq:(Medium) rs968891165 Functional Loss SNV dbSNP153 33..33 33 - - - 59133 RMVar_ID_59133 Human_SNP_ID_705638657 m1A Human chr22 - 45310045 45310045 45310045 GGCGGGGCAAGGGGATGGTTCTCGGGGAGGGGACTGCGCAGGCACGCGGGCTAGAAGCGAGAGCG GGCGGGGCAAGGGGATGGTTCTCGGGGAGGGGGCTGCGCAGGCACGCGGGCTAGAAGCGAGAGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:45309958..45310109 26863196 MeRIP-seq:(Medium) rs1344806362 Functional Loss SNV dbSNP153 33..33 33 - - - 59134 RMVar_ID_59134 Human_SNP_ID_705638968 m1A Human chr22 + 45311151 45311141 45311151 GGCGTCTTAGGAGTCGTGGGGAGGAGATGCTAAGCAGCAGGTGAGCTGATTCTTGAAGGTTGAGC GGCGTCTTAGGAGTCGTGGGGAG__________GCAGCAGGTGAGCTGATTCTTGAAGGTTGAGC GGAGATGCTAA G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45311146..45311225 26863196 MeRIP-seq:(Medium) rs1166269105 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_3678504,Human_RBP_ID_5389521,Human_RBP_ID_9432930,Human_RBP_ID_18952686 RMVar_hsa_circ_214974,RMVar_hsa_circ_374596 59135 RMVar_ID_59135 Human_SNP_ID_705669276 m1A Human chr22 + 45428557 45428557 45428557 CTTGGTGTGGCCTCTGGGAGCTCAGAGCCATCACTGGAGTCACGGGAAGGGGCATCAGGGCGGGA CTTGGTGTGGCCTCTGGGAGCTCAGAGCCATCCCTGGAGTCACGGGAAGGGGCATCAGGGCGGGA A C RIBC2 Ensembl:ENSG00000128408 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45428550..45428747 26863196 MeRIP-seq:(Medium) rs1031758363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352034 59136 RMVar_ID_59136 Human_SNP_ID_705688841 m1A Human chr22 + 45502811 45502811 45502811 CCGGCAGGGGGCGCCGGGGAGGGAGGACCAGGAGACCCGCGGCCCCGCCTCCGCCGCGCCCTCCT CCGGCAGGGGGCGCCGGGGAGGGAGGACCAGGGGACCCGCGGCCCCGCCTCCGCCGCGCCCTCCT A G FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45502749..45502839 26863196 MeRIP-seq:(Medium) rs1057333414 Functional Loss SNV dbSNP153 33..33 33 - - - 59137 RMVar_ID_59137 Human_SNP_ID_705688899 m1A Human chr22 - 45502949 45502947 45502950 GGCGGGCGACGGGCGGTGGGCGGCGGCGGACAAAGGCGCGGGCGCGGTCCTGGGGCAGCGGCGCG GGCGGGCGACGGGCGGTGGGCGGCGGCGGAC___GGCGCGGGCGCGGTCCTGGGGCAGCGGCGCG CTTT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:45502851..45503000 26863410 MeRIP-seq:(Medium) rs1288847186 Functional Loss DEL dbSNP153 32..34 33 - - - 59138 RMVar_ID_59138 Human_SNP_ID_705688914 m1A Human chr22 - 45502973 45502973 45502973 GACGGCGCGGCGCGCTCCATGGGCGGCGGGCGACGGGCGGTGGGCGGCGGCGGACAAAGGCGCGG GACGGCGCGGCGCGCTCCATGGGCGGCGGGCGGCGGGCGGTGGGCGGCGGCGGACAAAGGCGCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:45502876..45503075 26863410 MeRIP-seq:(Medium) rs1042898210 Functional Loss SNV dbSNP153 33..33 33 - - - 59139 RMVar_ID_59139 Human_SNP_ID_705692300 m1A Human chr22 - 45515960 45515960 45515960 CAGGCTCTGTCTCCTGTCCTTGTATACCCCCGACATCCATGCCAGCATGTGGCAGCTACAGAGTT CAGGCTCTGTCTCCTGTCCTTGTATACCCCCGTCATCCATGCCAGCATGTGGCAGCTACAGAGTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45515958..45516363 26863196 MeRIP-seq:(Medium) rs544978831 Functional Loss SNV dbSNP153 33..33 33 - - - 59140 RMVar_ID_59140 Human_SNP_ID_705694226 m1A Human chr22 - 45523055 45523055 45523055 AAATTATAAACCCACCATGAGCAGAAGCCCCTATGCCTCCCTGTTTCCCCCACGGCACATCCTGC AAATTATAAACCCACCATGAGCAGAAGCCCCTGTGCCTCCCTGTTTCCCCCACGGCACATCCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45523050..45523323 26863196 MeRIP-seq:(Medium) rs770010387 Functional Loss SNV dbSNP153 33..33 33 - - - 59141 RMVar_ID_59141 Human_SNP_ID_705694794 m1A Human chr22 + 45525086 45525079 45525087 AGCCTAACTCCATCTCAAAGAAAGAAAGAAAGAGAGAAAGAGAGAAAGGGAAAGAGAGAGAGAGA AGCCTAACTCCATCTCAAAGAAAGAA________AGAAAGAGAGAAAGGGAAAGAGAGAGAGAGA AAGAAAGAG A FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45525084..45525219 26863196 MeRIP-seq:(Medium) rs201381036 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_33304,RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_321914,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986 59142 RMVar_ID_59142 Human_SNP_ID_705694805 m1A Human chr22 + 45525104 45525097 45525105 AGAAAGAAAGAAAGAGAGAAAGAGAGAAAGGGAAAGAGAGAGAGAGAGAGAAAGAAAAACAGAGA AGAAAGAAAGAAAGAGAGAAAGAGAG________AGAGAGAGAGAGAGAGAAAGAAAAACAGAGA GAAAGGGAA G FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45525101..45525225 26863196 MeRIP-seq:(Medium) rs200167340 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_33304,RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_321914,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986 59143 RMVar_ID_59143 Human_SNP_ID_705694808 m1A Human chr22 + 45525099 45525099 45525099 CTCAAAGAAAGAAAGAAAGAGAGAAAGAGAGAAAGGGAAAGAGAGAGAGAGAGAGAAAGAAAAAC CTCAAAGAAAGAAAGAAAGAGAGAAAGAGAGAGAGGGAAAGAGAGAGAGAGAGAGAAAGAAAAAC A G FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45525093..45525213 26863196 MeRIP-seq:(Medium) rs1346226856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33304,RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_321914,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986 59144 RMVar_ID_59144 Human_SNP_ID_705695665 m1A Human chr22 + 45527964 45527964 45527964 GTGGACAGGTCTTCCAGGCATGCTGTGTCAAGAGCCAGGAGACCGGAGATTTGGATGTCGGGGGC GTGGACAGGTCTTCCAGGCATGCTGTGTCAAGGGCCAGGAGACCGGAGATTTGGATGTCGGGGGC A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45527915..45528064 26863196 MeRIP-seq:(Medium) rs754274542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582744,Human_RBP_ID_22768336 Human_Splice_Rec_2175455,Human_Splice_Rec_2175469,Human_Splice_Rec_2175479,Human_Splice_Rec_2175507,Human_Splice_Rec_2175535,Human_Splice_Rec_2175567,Human_Splice_Rec_2175595,Human_Splice_Rec_2175627,Human_Splice_Rec_2175633,Human_Splice_Rec_2175639 Human_miRNA_ID_2084658,Human_miRNA_ID_2084659 RMVar_hsa_circ_33304,RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_321914,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_285503,RMVar_hsa_circ_305067,RMVar_hsa_circ_114381,RMVar_hsa_circ_214987,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_214988,RMVar_hsa_circ_48218 59145 RMVar_ID_59145 Human_SNP_ID_705696548 m1A Human chr22 + 45531323 45531323 45531323 CAAGAGGACCCATATCTGAATGACCGCTGCCGAGGTGAGACTCGGGCGTCTCCCATCAGTTGGTA CAAGAGGACCCATATCTGAATGACCGCTGCCGCGGTGAGACTCGGGCGTCTCCCATCAGTTGGTA A C FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45531217..45531370 26863196 MeRIP-seq:(Medium) rs1330885689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780951,Human_RBP_ID_22455068 Human_Splice_Rec_2175456,Human_Splice_Rec_2175480,Human_Splice_Rec_2175481,Human_Splice_Rec_2175508,Human_Splice_Rec_2175509,Human_Splice_Rec_2175536,Human_Splice_Rec_2175537,Human_Splice_Rec_2175568,Human_Splice_Rec_2175569,Human_Splice_Rec_2175596,Human_Splice_Rec_2175597,Human_Splice_Rec_2175628,Human_Splice_Rec_2175640,Human_Splice_Rec_2175641 RMVar_hsa_circ_33304,RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_305067,RMVar_hsa_circ_114381,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_214988,RMVar_hsa_circ_48218,RMVar_hsa_circ_340737,RMVar_hsa_circ_214991 59146 RMVar_ID_59146 Human_SNP_ID_705696766 m1A Human chr22 + 45532169 45532169 45532169 ATTCTTAAATGATGCAGTCAGTGTACAGTGACAGTTGGTCCAGGGGCGCTGTCCAGGGGCCTGGT ATTCTTAAATGATGCAGTCAGTGTACAGTGACTGTTGGTCCAGGGGCGCTGTCCAGGGGCCTGGT A T FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45532167..45532420 26863196 MeRIP-seq:(Medium) rs561741207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_305067,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_48218,RMVar_hsa_circ_340737,RMVar_hsa_circ_214991 59147 RMVar_ID_59147 Human_SNP_ID_705697230 m1A Human chr22 + 45533814 45533814 45533814 GCAGCCACAGCTGCCGGCTTGGAGAATCCTGCATCAACACAGTGGGCTCTTTCCGCTGCCAGCGG GCAGCCACAGCTGCCGGCTTGGAGAATCCTGCCTCAACACAGTGGGCTCTTTCCGCTGCCAGCGG A C FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45533712..45533853 26863196 MeRIP-seq:(Medium) rs140981949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64858 Human_Splice_Rec_2175484,Human_Splice_Rec_2175485,Human_Splice_Rec_2175512,Human_Splice_Rec_2175513,Human_Splice_Rec_2175540,Human_Splice_Rec_2175541,Human_Splice_Rec_2175572,Human_Splice_Rec_2175573,Human_Splice_Rec_2175600,Human_Splice_Rec_2175601,Human_Splice_Rec_2175636,Human_Splice_Rec_2175644,Human_Splice_Rec_2175645,Human_Splice_Rec_2175652,Human_Splice_Rec_2175653,Human_Splice_Rec_2175658,Human_Splice_Rec_2175659,Human_Splice_Rec_2175661 Human_miRNA_ID_1989259,Human_miRNA_ID_1989260 RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_3569,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_305067,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_48218,RMVar_hsa_circ_340737,RMVar_hsa_circ_99808,RMVar_hsa_circ_214991,RMVar_hsa_circ_102718,RMVar_hsa_circ_214992,RMVar_hsa_circ_214993 59148 RMVar_ID_59148 Human_SNP_ID_705697231 m1A Human chr22 + 45533814 45533814 45533814 GCAGCCACAGCTGCCGGCTTGGAGAATCCTGCATCAACACAGTGGGCTCTTTCCGCTGCCAGCGG GCAGCCACAGCTGCCGGCTTGGAGAATCCTGCGTCAACACAGTGGGCTCTTTCCGCTGCCAGCGG A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45533712..45533853 26863196 MeRIP-seq:(Medium) rs140981949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64858 Human_Splice_Rec_2175484,Human_Splice_Rec_2175485,Human_Splice_Rec_2175512,Human_Splice_Rec_2175513,Human_Splice_Rec_2175540,Human_Splice_Rec_2175541,Human_Splice_Rec_2175572,Human_Splice_Rec_2175573,Human_Splice_Rec_2175600,Human_Splice_Rec_2175601,Human_Splice_Rec_2175636,Human_Splice_Rec_2175644,Human_Splice_Rec_2175645,Human_Splice_Rec_2175652,Human_Splice_Rec_2175653,Human_Splice_Rec_2175658,Human_Splice_Rec_2175659,Human_Splice_Rec_2175661 Human_miRNA_ID_1989259,Human_miRNA_ID_1989260 RMVar_hsa_circ_214982,RMVar_hsa_circ_81713,RMVar_hsa_circ_103434,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_323210,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_108725,RMVar_hsa_circ_3569,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214985,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_305067,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_48218,RMVar_hsa_circ_340737,RMVar_hsa_circ_99808,RMVar_hsa_circ_214991,RMVar_hsa_circ_102718,RMVar_hsa_circ_214992,RMVar_hsa_circ_214993 59149 RMVar_ID_59149 Human_SNP_ID_705699381 m1A Human chr22 + 45542200 45542200 45542200 CGCGCCACCTGCTGAGCCCTGTGGGAAGGGACATCGCTGCGTGAACTCTCCCGGCAGTTTCCGCT CGCGCCACCTGCTGAGCCCTGTGGGAAGGGACGTCGCTGCGTGAACTCTCCCGGCAGTTTCCGCT A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:45542176..45542200 26863196 MeRIP-seq:(Medium) rs1401880689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833125,Human_RBP_ID_22454765,Human_RBP_ID_22768340 Human_Splice_Rec_2175490,Human_Splice_Rec_2175491,Human_Splice_Rec_2175518,Human_Splice_Rec_2175519,Human_Splice_Rec_2175546,Human_Splice_Rec_2175547,Human_Splice_Rec_2175578,Human_Splice_Rec_2175579,Human_Splice_Rec_2175606,Human_Splice_Rec_2175607,Human_Splice_Rec_2175650,Human_Splice_Rec_2175664,Human_Splice_Rec_2175665 Human_miRNA_ID_3011894,Human_miRNA_ID_3011895 RMVar_hsa_circ_81713,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_3569,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_214991,RMVar_hsa_circ_214994,RMVar_hsa_circ_85184,RMVar_hsa_circ_308455,RMVar_hsa_circ_327117,RMVar_hsa_circ_345430,RMVar_hsa_circ_323201,RMVar_hsa_circ_285050,RMVar_hsa_circ_214996,RMVar_hsa_circ_214997,RMVar_hsa_circ_214998,RMVar_hsa_circ_214995,RMVar_hsa_circ_102453,RMVar_hsa_circ_127744,RMVar_hsa_circ_214999,RMVar_hsa_circ_215000 59150 RMVar_ID_59150 Human_SNP_ID_705699704 m1A Human chr22 + 45543406 45543404 45543407 CTGAGTCAGCCCACCCCTCACTTTCAGATGTCAACGAGTGCCAGCGCTACCCCGGGCGCCTGTGT CTGAGTCAGCCCACCCCTCACTTTCAGATGT___CGAGTGCCAGCGCTACCCCGGGCGCCTGTGT TCAA T FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr22:45543401..45543475;chr22:45543401..45543450 26863196 MeRIP-seq:(Medium) rs1376136770 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_932124,Human_RBP_ID_17989644,Human_RBP_ID_22454766,Human_RBP_ID_22768477 Human_Splice_Rec_2175492,Human_Splice_Rec_2175520,Human_Splice_Rec_2175548,Human_Splice_Rec_2175580,Human_Splice_Rec_2175608,Human_Splice_Rec_2175666 RMVar_hsa_circ_81713,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_340372,RMVar_hsa_circ_289613,RMVar_hsa_circ_3569,RMVar_hsa_circ_95602,RMVar_hsa_circ_107083,RMVar_hsa_circ_343435,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_214991,RMVar_hsa_circ_16850,RMVar_hsa_circ_214994,RMVar_hsa_circ_85184,RMVar_hsa_circ_308455,RMVar_hsa_circ_327117,RMVar_hsa_circ_345430,RMVar_hsa_circ_285050,RMVar_hsa_circ_214996,RMVar_hsa_circ_214997,RMVar_hsa_circ_214995,RMVar_hsa_circ_102453,RMVar_hsa_circ_127744,RMVar_hsa_circ_214999,RMVar_hsa_circ_215000,RMVar_hsa_circ_273735,RMVar_hsa_circ_376100,RMVar_hsa_circ_34592,RMVar_hsa_circ_215001,RMVar_hsa_circ_215002 59151 RMVar_ID_59151 Human_SNP_ID_705705007 m1A Human chr22 + 45563003 45563003 45563003 TAACCTACTACCACCTCTCTTTCCCCACCAACATCCAAGCGCCCGCGGTGGTTTTCCGCATGGGC TAACCTACTACCACCTCTCTTTCCCCACCAACGTCCAAGCGCCCGCGGTGGTTTTCCGCATGGGC A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45562953..45563302 26863196 MeRIP-seq:(Medium) rs755837069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17660613,Human_RBP_ID_18516463,Human_RBP_ID_22768481,Human_RBP_ID_27495408 Human_Splice_Rec_2175500,Human_Splice_Rec_2175528 RMVar_hsa_circ_81713,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_289613,RMVar_hsa_circ_107083,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_16850,RMVar_hsa_circ_345430,RMVar_hsa_circ_80908,RMVar_hsa_circ_111789,RMVar_hsa_circ_215004,RMVar_hsa_circ_215005 59152 RMVar_ID_59152 Human_SNP_ID_705705008 m1A Human chr22 + 45563003 45563003 45563003 TAACCTACTACCACCTCTCTTTCCCCACCAACATCCAAGCGCCCGCGGTGGTTTTCCGCATGGGC TAACCTACTACCACCTCTCTTTCCCCACCAACTTCCAAGCGCCCGCGGTGGTTTTCCGCATGGGC A T FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45562953..45563302 26863196 MeRIP-seq:(Medium) rs755837069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17660613,Human_RBP_ID_18516463,Human_RBP_ID_22768481,Human_RBP_ID_27495408 Human_Splice_Rec_2175500,Human_Splice_Rec_2175528 RMVar_hsa_circ_81713,RMVar_hsa_circ_214983,RMVar_hsa_circ_119686,RMVar_hsa_circ_289613,RMVar_hsa_circ_107083,RMVar_hsa_circ_103061,RMVar_hsa_circ_214984,RMVar_hsa_circ_214986,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_16850,RMVar_hsa_circ_345430,RMVar_hsa_circ_80908,RMVar_hsa_circ_111789,RMVar_hsa_circ_215004,RMVar_hsa_circ_215005 59153 RMVar_ID_59153 Human_SNP_ID_705708309 m1A Human chr22 + 45574606 45574606 45574606 ATGCGTGTTCGACCCCGTGCACACCATCTCCCACACCGTCATCTCGCTGCCTACCTTCCGCGAGT ATGCGTGTTCGACCCCGTGCACACCATCTCCCGCACCGTCATCTCGCTGCCTACCTTCCGCGAGT A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr22:45565687..45577061;chr22:45574418..45574726 26863196 MeRIP-seq:(Medium) rs760283248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27495412 Human_Splice_Rec_2175556,Human_Splice_Rec_2175557 Human_miRNA_ID_2066261,Human_miRNA_ID_2704105,Human_miRNA_ID_2935418 RMVar_hsa_circ_289613,RMVar_hsa_circ_107083,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_16850,RMVar_hsa_circ_345430,RMVar_hsa_circ_114639,RMVar_hsa_circ_111789,RMVar_hsa_circ_215004,RMVar_hsa_circ_293012,RMVar_hsa_circ_215007,RMVar_hsa_circ_91015,RMVar_hsa_circ_215008,RMVar_hsa_circ_215006 59154 RMVar_ID_59154 Human_SNP_ID_705709112 m1A Human chr22 - 45577069 45577067 45577069 CATGCCGTCCATGTAACGCTTGATGATGTCAAAAGAGTCCCGCAGGTTCCCTTCCGTGATGTCGA CATGCCGTCCATGTAACGCTTGATGATGTCAA__GAGTCCCGCAGGTTCCCTTCCGTGATGTCGA CTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:45577018..45577916 32194978 MeRIP-seq:(Medium) rs763734568 Functional Loss DEL dbSNP153 33..34 33 - - - 59155 RMVar_ID_59155 Human_SNP_ID_705712904 m1A Human chr22 - 45590784 45590784 45590784 CCCTACCCCTCACTCTCCAGGCAGGTACCCCCAAGCCAGGAACTTGGAGTCGCCCTCGATAGGCC CCCTACCCCTCACTCTCCAGGCAGGTACCCCCGAGCCAGGAACTTGGAGTCGCCCTCGATAGGCC T C LINC01589 RNACentral:URS0000D5BDD9 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45590778..45590939 26863196 MeRIP-seq:(Medium) rs747117864 Functional Loss SNV dbSNP153 33..33 33 - - - 59156 RMVar_ID_59156 Human_SNP_ID_705712905 m1A Human chr22 - 45590784 45590784 45590784 CCCTACCCCTCACTCTCCAGGCAGGTACCCCCAAGCCAGGAACTTGGAGTCGCCCTCGATAGGCC CCCTACCCCTCACTCTCCAGGCAGGTACCCCCCAGCCAGGAACTTGGAGTCGCCCTCGATAGGCC T G LINC01589 RNACentral:URS0000D5BDD9 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45590778..45590939 26863196 MeRIP-seq:(Medium) rs747117864 Functional Loss SNV dbSNP153 33..33 33 - - - 59157 RMVar_ID_59157 Human_SNP_ID_705714253 m1A Human chr22 - 45594751 45594748 45594752 ACCCAACCATCTGCTCATCCATCCATCCATCTATCCACTCACCCATCCATCTATCCATCCATCCA ACCCAACCATCTGCTCATCCATCCATCCATC____CACTCACCCATCCATCTATCCATCCATCCA GGATA G LINC01589,LINC01589:2 RNACentral:URS0000D5BDD9,RNACentral:URS00009AD2B3 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45594744..45594929 26863196 MeRIP-seq:(Medium) rs967813515 Functional Loss DEL dbSNP153 32..35 33 - - - 59158 RMVar_ID_59158 Human_SNP_ID_705718285 m1A Human chr22 - 45607861 45607861 45607861 GCCACTCCTCCATTCTTAGCTCCACATGGGGCACCCACATCTTCCCCCTCCCAGAGCCCCCTCCC GCCACTCCTCCATTCTTAGCTCCACATGGGGCCCCCACATCTTCCCCCTCCCAGAGCCCCCTCCC T G LINC01589,LINC01589:2,LINC01589:3,LINC01589:4,LINC01589:5 RNACentral:URS0000D5BDD9,RNACentral:URS00008BED00,RNACentral:URS00008B3DCC,RNACentral:URS0000D5840C,RNACentral:URS0000D58512 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45607859..45607942 26863196 MeRIP-seq:(Medium) rs1348883056 Functional Loss SNV dbSNP153 33..33 33 - - - 59159 RMVar_ID_59159 Human_SNP_ID_705734272 m1A Human chr22 - 45671976 45671976 45671976 AAGGGGGAGGATGACGAGGAGGGAGGAGTAGGATGGCGAGGAGGAAGGGGGAGGCCTCGCCCTAC AAGGGGGAGGATGACGAGGAGGGAGGAGTAGGTTGGCGAGGAGGAAGGGGGAGGCCTCGCCCTAC T A lnc-SMC1B-8 RNACentral:URS00008C20DE lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:45671874..45671986 26863410 MeRIP-seq:(Medium) rs1490794495 Functional Loss SNV dbSNP153 33..33 33 - - - 59160 RMVar_ID_59160 Human_SNP_ID_705748767 m1A Human chr22 + 45729447 45729447 45729447 TGTTTTACAGAGTTACACTGTTAGACCTTATGATAGCCAAGATAACGAGTGATGAGCCACTCACC TGTTTTACAGAGTTACACTGTTAGACCTTATGGTAGCCAAGATAACGAGTGATGAGCCACTCACC A G ATXN10 Ensembl:ENSG00000130638 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:45729432..45738486 32194978 MeRIP-seq:(Medium) rs745479298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1308428,Human_RBP_ID_8552557,Human_RBP_ID_17702259,Human_RBP_ID_17989567,Human_RBP_ID_23952572 Human_Splice_Rec_2175686,Human_Splice_Rec_2175708,Human_Splice_Rec_2175730,Human_Splice_Rec_2175756,Human_Splice_Rec_2175760 Human_miRNA_ID_678249 RMVar_hsa_circ_97228,RMVar_hsa_circ_84094,RMVar_hsa_circ_215010,RMVar_hsa_circ_113082,RMVar_hsa_circ_270513,RMVar_hsa_circ_215012,RMVar_hsa_circ_215013,RMVar_hsa_circ_315440,RMVar_hsa_circ_274330,RMVar_hsa_circ_215024,RMVar_hsa_circ_28976,RMVar_hsa_circ_215022,RMVar_hsa_circ_215014,RMVar_hsa_circ_215015,RMVar_hsa_circ_315660,RMVar_hsa_circ_278740,RMVar_hsa_circ_215023,RMVar_hsa_circ_272785,RMVar_hsa_circ_275917,RMVar_hsa_circ_108537,RMVar_hsa_circ_215026,RMVar_hsa_circ_215025,RMVar_hsa_circ_215029,RMVar_hsa_circ_313013,RMVar_hsa_circ_324029,RMVar_hsa_circ_215031,RMVar_hsa_circ_215034,RMVar_hsa_circ_90753,RMVar_hsa_circ_270309,RMVar_hsa_circ_351949,RMVar_hsa_circ_215035,RMVar_hsa_circ_215033 59161 RMVar_ID_59161 Human_SNP_ID_705751134 m1A Human chr22 - 45738780 45738780 45738780 AAACCTGCAGATAGCCGAGCAGCTCAGTATTCACAGTCATTTCGCACAGGACGTCGAGAAGCCTA AAACCTGCAGATAGCCGAGCAGCTCAGTATTCGCAGTCATTTCGCACAGGACGTCGAGAAGCCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45738683..45738800 26863196 MeRIP-seq:(Medium) rs1349801018 Functional Loss SNV dbSNP153 33..33 33 - - - 59162 RMVar_ID_59162 Human_SNP_ID_705758993 m1A Human chr22 + 45768579 45768579 45768579 AAACCTCTAGATCTAACTGTCAGTTTAGAGAAAATACAGGCATGAGAGAGAAGGGCATGTTAAAG AAACCTCTAGATCTAACTGTCAGTTTAGAGAAGATACAGGCATGAGAGAGAAGGGCATGTTAAAG A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45768576..45768704 26863196 MeRIP-seq:(Medium) rs1423141422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2722232,Human_RBP_ID_14521408 RMVar_hsa_circ_215024,RMVar_hsa_circ_108537,RMVar_hsa_circ_90837,RMVar_hsa_circ_215038 59163 RMVar_ID_59163 Human_SNP_ID_705759196 m1A Human chr22 + 45769521 45769521 45769521 ACCGTGGAGTTGGGCCTTGAGGAATGGTGGGTAGCAGTTATGTGGCGATGAAGAGACTATTTCAA ACCGTGGAGTTGGGCCTTGAGGAATGGTGGGTGGCAGTTATGTGGCGATGAAGAGACTATTTCAA A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45769405..45769592 26863196 MeRIP-seq:(Medium) rs1477167186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2722244,Human_RBP_ID_23014508,Human_RBP_ID_23952643 RMVar_hsa_circ_215024,RMVar_hsa_circ_108537,RMVar_hsa_circ_90837,RMVar_hsa_circ_215038 59164 RMVar_ID_59164 Human_SNP_ID_705790254 m1A Human chr22 + 45890480 45890478 45890480 CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGCGAGTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGC__GTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT CGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45890350..45890942 26863196 MeRIP-seq:(Medium) rs1394079673 Functional Loss DEL dbSNP153 32..33 33 - - - 59165 RMVar_ID_59165 Human_SNP_ID_705790259 m1A Human chr22 + 45890480 45890480 45890480 CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGCGAGTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGCGGGTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45890350..45890942 26863196 MeRIP-seq:(Medium) rs370704549 Functional Loss SNV dbSNP153 33..33 33 - - - 59166 RMVar_ID_59166 Human_SNP_ID_705790260 m1A Human chr22 + 45890480 45890480 45890480 CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGCGAGTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT CGAGTGTGTGAGGGGCGTGTGTGTGCGGGGCGTGTGTGTGAGGGGCGAGTGTGTGCGGGGCGAGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45890350..45890942 26863196 MeRIP-seq:(Medium) rs370704549 Functional Loss SNV dbSNP153 33..33 33 - - - 59167 RMVar_ID_59167 Human_SNP_ID_705790523 m1A Human chr22 - 45890842 45890842 45890842 CTCCCTGCCCCGCACACACACGCCCCGCACACACTCGCCCCGCACACACTCGCCCCGCACACACT CTCCCTGCCCCGCACACACACGCCCCGCACACCCTCGCCCCGCACACACTCGCCCCGCACACACT T G BX324167.1 Ensembl:ENSG00000235091 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45890758..45890896 26863196 MeRIP-seq:(Medium) rs1489028092 Functional Loss SNV dbSNP153 33..33 33 - - - 59168 RMVar_ID_59168 Human_SNP_ID_705796955 m1A Human chr22 - 45912430 45912430 45912430 TTTCCCCATGTCTACCCTGGACCCCACACCCCACACCCCCCAACAAGCCCTGCAGACTTCTCATC TTTCCCCATGTCTACCCTGGACCCCACACCCCCCACCCCCCAACAAGCCCTGCAGACTTCTCATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45912412..45912529 26863196 MeRIP-seq:(Medium) rs1442284159 Functional Loss SNV dbSNP153 33..33 33 - - - 59169 RMVar_ID_59169 Human_SNP_ID_705797047 m1A Human chr22 - 45912698 45912698 45912698 TGTCCCCAGCCAGCCAGAGAGCTCCTCCTTGAACCCCCCATCCCCTCTGTACTTATCATGATCTC TGTCCCCAGCCAGCCAGAGAGCTCCTCCTTGATCCCCCCATCCCCTCTGTACTTATCATGATCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45912647..45912751 26863196 MeRIP-seq:(Medium) rs1173599040 Functional Loss SNV dbSNP153 33..33 33 - - - 59170 RMVar_ID_59170 Human_SNP_ID_705797048 m1A Human chr22 - 45912698 45912698 45912698 TGTCCCCAGCCAGCCAGAGAGCTCCTCCTTGAACCCCCCATCCCCTCTGTACTTATCATGATCTC TGTCCCCAGCCAGCCAGAGAGCTCCTCCTTGACCCCCCCATCCCCTCTGTACTTATCATGATCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45912647..45912751 26863196 MeRIP-seq:(Medium) rs1173599040 Functional Loss SNV dbSNP153 33..33 33 - - - 59171 RMVar_ID_59171 Human_SNP_ID_705802127 m1A Human chr22 - 45928577 45928575 45928577 TGGTGATGGTCCCCACGGGTGGGCAGGAGACAAAGAGGACAGCCACAGGAAAGGGCTCTGATGAT TGGTGATGGTCCCCACGGGTGGGCAGGAGACA__GAGGACAGCCACAGGAAAGGGCTCTGATGAT CTT C WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45928573..45928958 26863196 MeRIP-seq:(Medium) rs1011378522 Functional Loss DEL dbSNP153 33..34 33 - - - 59172 RMVar_ID_59172 Human_SNP_ID_705802131 m1A Human chr22 - 45928585 45928585 45928585 AAGGCGGCTGGTGATGGTCCCCACGGGTGGGCAGGAGACAAAGAGGACAGCCACAGGAAAGGGCT AAGGCGGCTGGTGATGGTCCCCACGGGTGGGCGGGAGACAAAGAGGACAGCCACAGGAAAGGGCT T C WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45928582..45928827 26863196 MeRIP-seq:(Medium) rs942167483 Functional Loss SNV dbSNP153 33..33 33 - - - 59173 RMVar_ID_59173 Human_SNP_ID_705802456 m1A Human chr22 - 45929189 45929189 45929189 TGTGGTTCACCTACCTGGAGGCATCTGGGAGGACTCCCTGGAGGAGGAGGAGAAAGAGGAGAAGG TGTGGTTCACCTACCTGGAGGCATCTGGGAGGGCTCCCTGGAGGAGGAGGAGAAAGAGGAGAAGG T C WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45929187..45929456 26863196 MeRIP-seq:(Medium) rs1042150880 Functional Loss SNV dbSNP153 33..33 33 - - - 59174 RMVar_ID_59174 Human_SNP_ID_705802457 m1A Human chr22 - 45929189 45929189 45929189 TGTGGTTCACCTACCTGGAGGCATCTGGGAGGACTCCCTGGAGGAGGAGGAGAAAGAGGAGAAGG TGTGGTTCACCTACCTGGAGGCATCTGGGAGGCCTCCCTGGAGGAGGAGGAGAAAGAGGAGAAGG T G WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45929187..45929456 26863196 MeRIP-seq:(Medium) rs1042150880 Functional Loss SNV dbSNP153 33..33 33 - - - 59175 RMVar_ID_59175 Human_SNP_ID_705802545 m1A Human chr22 + 45929378 45929359 45929379 ATTCCTTTATCCATCCATCTATTCACCCATCCACCCACTCACCCATCCATCCTTCCATCCACCCG ATTCCTTTATCCAT____________________CCACTCACCCATCCATCCTTCCATCCACCCG TCCATCTATTCACCCATCCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45929146..45929452 26863196 MeRIP-seq:(Medium) rs1369974004 Functional Loss DEL dbSNP153 15..34 33 - - - 59176 RMVar_ID_59176 Human_SNP_ID_705803044 m1A Human chr22 + 45929722 45929722 45929722 ATCCACCCATCTTTCCATCCACCCGTGAATCCACTCACCCATCCACCCACCGATCCATCCTTTCA ATCCACCCATCTTTCCATCCACCCGTGAATCCGCTCACCCATCCACCCACCGATCCATCCTTTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:45929686..45929893 26863196 MeRIP-seq:(Medium) rs1309097566 Functional Loss SNV dbSNP153 33..33 33 - - - 59177 RMVar_ID_59177 Human_SNP_ID_705803098 m1A Human chr22 + 45929778 45929778 45929778 ATCCTTTCATTCATCTGTCTACTTATCCTTCCATCCACCCACCGATCCACTCAACCATCTACCCA ATCCTTTCATTCATCTGTCTACTTATCCTTCCGTCCACCCACCGATCCACTCAACCATCTACCCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:45929517..45929926 26863196 MeRIP-seq:(Medium) rs950088088 Functional Loss SNV dbSNP153 33..33 33 - - - 59178 RMVar_ID_59178 Human_SNP_ID_705803278 m1A Human chr22 - 45929922 45929906 45929922 TGGATGGATGGAAGGATGAGTGGGTGGATGGGAGGATAGATGGATGGGTAGATAGATGAGTGGAT TGGATGGATGGAAGGATGAGTGGGTGGATGGG________________TAGATAGATGAGTGGAT ACCCATCCATCTATCCT A WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45929522..45930164 26863196 MeRIP-seq:(Medium) rs1464343881 Functional Loss DEL dbSNP153 33..48 33 - - - 59179 RMVar_ID_59179 Human_SNP_ID_705803591 m1A Human chr22 - 45930407 45930397 45930407 TGAGATAGGGTGGCCAGCCAAGTGGAACGCCCAGCCGGCTCCGGCTCCGAGGCCTGGGGGCTGCA TGAGATAGGGTGGCCAGCCAAGTGGAACGCCC__________GGCTCCGAGGCCTGGGGGCTGCA CGGAGCCGGCT C WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45930405..45930643 26863196 MeRIP-seq:(Medium) rs200457501 Functional Loss DEL dbSNP153 33..42 33 - - - 59180 RMVar_ID_59180 Human_SNP_ID_705808109 m1A Human chr22 - 45943084 45943084 45943084 ACACACACATGCACACACACAAACACACGCACACACGTGCACACATGTGCACACTGCACACACAT ACACACACATGCACACACACAAACACACGCACGCACGTGCACACATGTGCACACTGCACACACAT T C WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45943082..45943165 26863196 MeRIP-seq:(Medium) rs1209999281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2722830 59181 RMVar_ID_59181 Human_SNP_ID_705809011 m1A Human chr22 - 45946203 45946203 45946203 CAGGAATGACAGGAGCTTCCAGGGCTAACAGGAGAGGCTGGAGGGTGAGGGCAGGGCTGGAGTAC CAGGAATGACAGGAGCTTCCAGGGCTAACAGGCGAGGCTGGAGGGTGAGGGCAGGGCTGGAGTAC T G WNT7B Ensembl:ENSG00000188064 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45946180..45946355 26863196 MeRIP-seq:(Medium) rs1449096998 Functional Loss SNV dbSNP153 33..33 33 - - - 59182 RMVar_ID_59182 Human_SNP_ID_705811191 m1A Human chr22 + 45953297 45953297 45953297 TCACAGTCACCGTGTCCTCGGCTTCCTCTCACAGTCACCACGTCCATGCCCCGCTTCCCCTCACA TCACAGTCACCGTGTCCTCGGCTTCCTCTCACGGTCACCACGTCCATGCCCCGCTTCCCCTCACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:45952953..45953368 26863196 MeRIP-seq:(Medium) rs1003573537 Functional Loss SNV dbSNP153 33..33 33 - - - 59183 RMVar_ID_59183 Human_SNP_ID_705818311 m1A Human chr22 - 45977090 45977090 45977090 GCCGCGGCGCTCGGCGAGGCGCTCACGGCCTCAGGCGGCTGCGCCTAGTGCAGGCTGCACCCGCC GCCGCGGCGCTCGGCGAGGCGCTCACGGCCTCGGGCGGCTGCGCCTAGTGCAGGCTGCACCCGCC T C WNT7B Ensembl:ENSG00000188064 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45977040..45977242 26863196 MeRIP-seq:(Medium) rs1238717036 Functional Loss SNV dbSNP153 33..33 33 - - - 59184 RMVar_ID_59184 Human_SNP_ID_705818312 m1A Human chr22 - 45977090 45977090 45977090 GCCGCGGCGCTCGGCGAGGCGCTCACGGCCTCAGGCGGCTGCGCCTAGTGCAGGCTGCACCCGCC GCCGCGGCGCTCGGCGAGGCGCTCACGGCCTCCGGCGGCTGCGCCTAGTGCAGGCTGCACCCGCC T G WNT7B Ensembl:ENSG00000188064 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45977040..45977242 26863196 MeRIP-seq:(Medium) rs1238717036 Functional Loss SNV dbSNP153 33..33 33 - - - 59185 RMVar_ID_59185 Human_SNP_ID_705828950 m1A Human chr22 - 46013960 46013960 46013960 CCCAGGAAGGCAGAGGGAACGGGCAGGCCCGGAGGAGCAGGCGGGAATGTGGAGGGGGGTTGGAA CCCAGGAAGGCAGAGGGAACGGGCAGGCCCGGTGGAGCAGGCGGGAATGTGGAGGGGGGTTGGAA T A lnc-PRR34-4 RNACentral:URS00008C257E lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46013909..46014118 26863196 MeRIP-seq:(Medium) rs906074957 Functional Loss SNV dbSNP153 33..33 33 - - - 59186 RMVar_ID_59186 Human_SNP_ID_705828968 m1A Human chr22 + 46014012 46014012 46014012 CTGCCTTCCTGGGAACCTCCCTCTATCTCCGCATCTTCCGCCGCTCCCTTCCCTGCGGCAGCCGG CTGCCTTCCTGGGAACCTCCCTCTATCTCCGCGTCTTCCGCCGCTCCCTTCCCTGCGGCAGCCGG A G BX537318.1 Ensembl:ENSG00000273145 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46013833..46014157 26863196 MeRIP-seq:(Medium) rs1198985730 Functional Loss SNV dbSNP153 33..33 33 - - - 59187 RMVar_ID_59187 Human_SNP_ID_705837006 m1A Human chr22 - 46044703 46044703 46044703 AGAGGGAAAGAAGGAGGAAAAGCAGGCCGGGGAGGGGAGGAAGAGAACCGCGCGGAGGCCGCGGC AGAGGGAAAGAAGGAGGAAAAGCAGGCCGGGGCGGGGAGGAAGAGAACCGCGCGGAGGCCGCGGC T G LINC00899 Ensembl:ENSG00000231711 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr22:46044588..46044870;chr22:46044659..46044994 26863196 MeRIP-seq:(Medium) rs1007650424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2175839 59188 RMVar_ID_59188 Human_SNP_ID_705838003 m1A Human chr22 + 46048478 46048478 46048478 CTGCCCCTCACACGTGTTCGTGCCGCATGCTGAGGCCCAGGGAGGGACCAAAGGCAGCTTCAGTG CTGCCCCTCACACGTGTTCGTGCCGCATGCTGCGGCCCAGGGAGGGACCAAAGGCAGCTTCAGTG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46048371..46048502 26863196 MeRIP-seq:(Medium) rs1403848364 Functional Loss SNV dbSNP153 33..33 33 - - - 59189 RMVar_ID_59189 Human_SNP_ID_705839318 m1A Human chr22 - 46053612 46053612 46053612 GCCTGCGGGGGCCTCCCCTGCCTCCCGTCCCCAGAGTCCCACAGAGGCGCAGACAACACGAGCGC GCCTGCGGGGGCCTCCCCTGCCTCCCGTCCCCGGAGTCCCACAGAGGCGCAGACAACACGAGCGC T C PRR34 Ensembl:ENSG00000182257 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46053608..46053704 26863196 MeRIP-seq:(Medium) rs1383379162 Functional Loss SNV dbSNP153 33..33 33 - - - 59190 RMVar_ID_59190 Human_SNP_ID_705844036 m1A Human chr22 + 46070584 46070584 46070584 CGCGCCCCTGCCCATCCCACGCCTCCCCGGGCACCGTGAACCACCCCCCAACCCAACTCCTCCAG CGCGCCCCTGCCCATCCCACGCCTCCCCGGGCGCCGTGAACCACCCCCCAACCCAACTCCTCCAG A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:46070551..46070850 26863196 MeRIP-seq:(Medium) rs1201756249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2723192,Human_RBP_ID_5600321 RMVar_hsa_circ_92627,RMVar_hsa_circ_215049 59191 RMVar_ID_59191 Human_SNP_ID_705844493 m1A Human chr22 - 46071693 46071693 46071693 GCGCGCCGGCCGCGCTTCCCCCGTTGCCGCCTATTTTATGTCTTTTGTCTCGGAGTTGGCACCTG GCGCGCCGGCCGCGCTTCCCCCGTTGCCGCCTGTTTTATGTCTTTTGTCTCGGAGTTGGCACCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46071645..46071796 26863196 MeRIP-seq:(Medium) rs1262990521 Functional Loss SNV dbSNP153 33..33 33 - - - 59192 RMVar_ID_59192 Human_SNP_ID_705845624 m1A Human chr22 - 46075378 46075378 46075378 GTGCAAAGACTCCAGCTTGCTGCGATTTCGGCAAGAGCATTCTCCTCTCTCCCCAAACATGCAAA GTGCAAAGACTCCAGCTTGCTGCGATTTCGGCCAGAGCATTCTCCTCTCTCCCCAAACATGCAAA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:46075330..46075452 32194978 MeRIP-seq:(Medium) rs778869059 Functional Loss SNV dbSNP153 33..33 33 - - - 59193 RMVar_ID_59193 Human_SNP_ID_705848430 m1A Human chr22 - 46084835 46084835 46084835 CCCACGGGCATCCCTGGGGTGGTGGAGAGCCCATGGCACAGTCATCCCCAGGTGTGGTCTGAGGA CCCACGGGCATCCCTGGGGTGGTGGAGAGCCCGTGGCACAGTCATCCCCAGGTGTGGTCTGAGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:46084830..46084986 26863196 MeRIP-seq:(Medium) rs891701813 Functional Loss SNV dbSNP153 33..33 33 - - - 59194 RMVar_ID_59194 Human_SNP_ID_705848476 m1A Human chr22 + 46085057 46085057 46085057 CTTATGTGGACAGGCGGTTCTGGGCGCCGGCCATTTGCAGACTGGGAGGAGTGGAAGTGAGGCCT CTTATGTGGACAGGCGGTTCTGGGCGCCGGCCCTTTGCAGACTGGGAGGAGTGGAAGTGAGGCCT A C MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46085049..46085124 26863196 MeRIP-seq:(Medium) rs1485126868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1136730,Human_RBP_ID_5101725,Human_RBP_ID_5600364 RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59195 RMVar_ID_59195 Human_SNP_ID_705848914 m1A Human chr22 + 46086476 46086476 46086476 GACGGGGGCCAGCAGGGCAGGAGCAGCGGGGAACCCTGGGTGGTGGAGATCCCCTGCCTTGGTCC GACGGGGGCCAGCAGGGCAGGAGCAGCGGGGACCCCTGGGTGGTGGAGATCCCCTGCCTTGGTCC A C MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46086426..46086600 26863196 MeRIP-seq:(Medium) rs1016503071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5203570,Human_RBP_ID_5601648,Human_RBP_ID_22723969 RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59196 RMVar_ID_59196 Human_SNP_ID_705848915 m1A Human chr22 + 46086476 46086476 46086476 GACGGGGGCCAGCAGGGCAGGAGCAGCGGGGAACCCTGGGTGGTGGAGATCCCCTGCCTTGGTCC GACGGGGGCCAGCAGGGCAGGAGCAGCGGGGAGCCCTGGGTGGTGGAGATCCCCTGCCTTGGTCC A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46086426..46086600 26863196 MeRIP-seq:(Medium) rs1016503071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5203570,Human_RBP_ID_5601648,Human_RBP_ID_22723969 RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59197 RMVar_ID_59197 Human_SNP_ID_705851279 m1A Human chr22 + 46094527 46094526 46094528 GGCCTAAGCTGGCCCTGTCCTGGGGGCCACACAGGGGTCCTGCAAGGAAGCACACCTCGGGGTGT GGCCTAAGCTGGCCCTGTCCTGGGGGCCACAC__GGGTCCTGCAAGGAAGCACACCTCGGGGTGT CAG C MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:46094517..46094626 32194978 MeRIP-seq:(Medium) rs981388962 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59198 RMVar_ID_59198 Human_SNP_ID_705851280 m1A Human chr22 + 46094527 46094527 46094527 GGCCTAAGCTGGCCCTGTCCTGGGGGCCACACAGGGGTCCTGCAAGGAAGCACACCTCGGGGTGT GGCCTAAGCTGGCCCTGTCCTGGGGGCCACACGGGGGTCCTGCAAGGAAGCACACCTCGGGGTGT A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:46094517..46094626 32194978 MeRIP-seq:(Medium) rs990125143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59199 RMVar_ID_59199 Human_SNP_ID_705851649 m1A Human chr22 - 46095919 46095837 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCC_________________________________ CGGCAGGTGAGGGCATTGGGGTGGTCCCAGCCAGCCCAGGGCGGCAGGTGAGGGCATTAGGGTGGTCCCAGCCAGCCCAGGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs1569157460 Functional Loss DEL dbSNP153 33..65 33 - - - 59200 RMVar_ID_59200 Human_SNP_ID_705851664 m1A Human chr22 - 46095919 46095878 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCC_________________________________ CGGCAGGTGAGGGCATTAGGGTGGTCCCAGCCAGCCCAGGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs1361248509 Functional Loss DEL dbSNP153 33..65 33 - - - 59201 RMVar_ID_59201 Human_SNP_ID_705851680 m1A Human chr22 + 46095915 46095915 46095915 GGTGAGGGCATTAGGGTGGTCCCAGCCAGCCCAGGGTGGCAGGTGAGGGCATTGGGGTGGTCCCA GGTGAGGGCATTAGGGTGGTCCCAGCCAGCCCGGGGTGGCAGGTGAGGGCATTGGGGTGGTCCCA A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46095865..46096287 26863196 MeRIP-seq:(Medium) rs866165502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2496868,Human_miRNA_ID_2498094,Human_miRNA_ID_2555550 RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59202 RMVar_ID_59202 Human_SNP_ID_705851682 m1A Human chr22 - 46095919 46095919 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCCTCCCTGGGCTGGCTGGGACCACCCTAATGCCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs13055228 Functional Loss SNV dbSNP153 33..33 33 - - - 59203 RMVar_ID_59203 Human_SNP_ID_705851683 m1A Human chr22 - 46095919 46095919 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCCGCCCTGGGCTGGCTGGGACCACCCTAATGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs13055228 Functional Loss SNV dbSNP153 33..33 33 - - - 59204 RMVar_ID_59204 Human_SNP_ID_705851684 m1A Human chr22 - 46095919 46095919 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCCCCCCTGGGCTGGCTGGGACCACCCTAATGCCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs13055228 Functional Loss SNV dbSNP153 33..33 33 - - - 59205 RMVar_ID_59205 Human_SNP_ID_705851735 m1A Human chr22 + 46096092 46096092 46096092 AGGCAGGGGGACCCAGGGTTATTAGAGTGGCTATCAGGACTCGCTGGGCCCCAGGGTGGGGGCTT AGGCAGGGGGACCCAGGGTTATTAGAGTGGCTGTCAGGACTCGCTGGGCCCCAGGGTGGGGGCTT A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46095880..46096250 26863196 MeRIP-seq:(Medium) rs1044572453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5600386,Human_RBP_ID_17988411,Human_RBP_ID_25678280 RMVar_hsa_circ_92627,RMVar_hsa_circ_215050,RMVar_hsa_circ_215049 59206 RMVar_ID_59206 Human_SNP_ID_705852724 m1A Human chr22 + 46099583 46099581 46099583 TAACAGAGGAAGGAGAACAGCGTGGGGACAGGAGAGGGGCAGGGACTGGGGAAGAGGAGACACAA TAACAGAGGAAGGAGAACAGCGTGGGGACAG__GAGGGGCAGGGACTGGGGAAGAGGAGACACAA GGA G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46099409..46099724;chr22:46099432..46099695 26863196 MeRIP-seq:(Medium) rs1355192595 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_65870,Human_RBP_ID_5101395,Human_RBP_ID_5204932,Human_RBP_ID_5324842,Human_RBP_ID_5601276,Human_RBP_ID_7091049 RMVar_hsa_circ_126840,RMVar_hsa_circ_88194,RMVar_hsa_circ_377553,RMVar_hsa_circ_378309,RMVar_hsa_circ_215052,RMVar_hsa_circ_47517,RMVar_hsa_circ_215053,RMVar_hsa_circ_215051,RMVar_hsa_circ_215056 59207 RMVar_ID_59207 Human_SNP_ID_705855470 m1A Human chr22 - 46108258 46108258 46108258 CCCGGGCTCCCCCTCCAGCCTCCCAGAGCAGCAAGTGTCCCGGGCAGGCCTCTGCTCCCAGCATT CCCGGGCTCCCCCTCCAGCCTCCCAGAGCAGCCAGTGTCCCGGGCAGGCCTCTGCTCCCAGCATT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46108209..46108326 26863196 MeRIP-seq:(Medium) rs1386807022 Functional Loss SNV dbSNP153 33..33 33 - - - 59208 RMVar_ID_59208 Human_SNP_ID_705857110 m1A Human chr22 + 46112949 46112949 46112949 GGGCAGGGGCCGCCTACACTGAGAAGTCTGACAGGCCTAGGTGCCACTTGCTGTGTGACCTTGGA GGGCAGGGGCCGCCTACACTGAGAAGTCTGACGGGCCTAGGTGCCACTTGCTGTGTGACCTTGGA A G MIRLET7BHG Ensembl:ENSG00000197182 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46112900..46113134 26863196 MeRIP-seq:(Medium) rs765526210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8119783 RMVar_hsa_circ_378309,RMVar_hsa_circ_215051 59209 RMVar_ID_59209 Human_SNP_ID_705884531 m1A Human chr22 + 46214250 46214250 46214250 GAGGTATGGGCGGTATGGCAAGGCGCGGGCCCATAGATGTGCAGGTCTGGAGATGTGTGCAGCGG GAGGTATGGGCGGTATGGCAAGGCGCGGGCCCGTAGATGTGCAGGTCTGGAGATGTGTGCAGCGG A G PPARA Ensembl:ENSG00000186951 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46214242..46214332 26863196 MeRIP-seq:(Medium) rs988741714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54495,RMVar_hsa_circ_52800,RMVar_hsa_circ_354322,RMVar_hsa_circ_368827,RMVar_hsa_circ_357932,RMVar_hsa_circ_215061 59210 RMVar_ID_59210 Human_SNP_ID_705884631 m1A Human chr22 + 46214512 46214512 46214512 CGAATCGGAGATGCGCGGGTCCGGAAATGTGCAGAGCGGAGATGTGTGGATCAGGAGATGTTGGG CGAATCGGAGATGCGCGGGTCCGGAAATGTGCGGAGCGGAGATGTGTGGATCAGGAGATGTTGGG A G PPARA Ensembl:ENSG00000186951 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46214226..46214621 26863196 MeRIP-seq:(Medium) rs4253730 Functional Loss SNV dbSNP153,PGA 33..33 33 - - - RMVar_hsa_circ_54495,RMVar_hsa_circ_52800,RMVar_hsa_circ_354322,RMVar_hsa_circ_368827,RMVar_hsa_circ_357932,RMVar_hsa_circ_215061 59211 RMVar_ID_59211 Human_SNP_ID_705892200 m1A Human chr22 - 46244255 46244255 46244255 ACTGCTTGCCTGCTTGCCCCCTGCCATCTCGCACTCAGCCCTGGGTGCCTGTGAAGCCTGGCCCC ACTGCTTGCCTGCTTGCCCCCTGCCATCTCGCCCTCAGCCCTGGGTGCCTGTGAAGCCTGGCCCC T G CDPF1 Ensembl:ENSG00000205643 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46244210..46244365 26863196 MeRIP-seq:(Medium) rs1170694194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121071,RMVar_hsa_circ_215067 59212 RMVar_ID_59212 Human_SNP_ID_705894008 m1A Human chr22 - 46250643 46250643 46250643 CCTAGTCCGCGGCGCGGGAGGGCAGGTGGGAGACTGGAGGCGCCCTCGCGCCCCTCAGCTATCCG CCTAGTCCGCGGCGCGGGAGGGCAGGTGGGAGGCTGGAGGCGCCCTCGCGCCCCTCAGCTATCCG T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46250529..46250642 26863196 MeRIP-seq:(Medium) rs796911682 Functional Loss SNV dbSNP153 33..33 33 - - - 59213 RMVar_ID_59213 Human_SNP_ID_705899213 m1A Human chr22 + 46268071 46268071 46268071 CATGGCCGCAGCCTCGCCTCTGCGCGACTGCCAGGTACACGGAGGCTGCCCCCAACCAGGTCCCC CATGGCCGCAGCCTCGCCTCTGCGCGACTGCCGGGTACACGGAGGCTGCCCCCAACCAGGTCCCC A G TTC38 Ensembl:ENSG00000075234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:46268030..46268113;chr22:46268031..46268108;chr22:46268045..46268265 26863196 MeRIP-seq:(Medium) rs1301700641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709169,Human_RBP_ID_5389528,Human_RBP_ID_19112346,Human_RBP_ID_23015525 Human_Splice_Rec_2176009,Human_Splice_Rec_2176019,Human_Splice_Rec_2176021,Human_Splice_Rec_2176033,Human_Splice_Rec_2176059 59214 RMVar_ID_59214 Human_SNP_ID_705905577 m1A Human chr22 - 46290527 46290526 46290528 CCCTCCTAACACCCTCCAGCCACGCTGCCCTAACACACTCACCCTCCAGCCATGCCACCCTAACA CCCTCCTAACACCCTCCAGCCACGCTGCCCT__CACACTCACCCTCCAGCCATGCCACCCTAACA GTT G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46290363..46290802 26863196 MeRIP-seq:(Medium) rs1473741118 Functional Loss DEL dbSNP153 32..33 33 - - - 59215 RMVar_ID_59215 Human_SNP_ID_705906454 m1A Human chr22 - 46293540 46293540 46293540 ACGGGTCCAAATCAGCACCAACAGAGCCCCCCAGGGGGCTCCAAGACTCGCCCCAGAGACAGCAG ACGGGTCCAAATCAGCACCAACAGAGCCCCCCCGGGGGCTCCAAGACTCGCCCCAGAGACAGCAG T G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:46293212..46293561 32194978 MeRIP-seq:(Medium) rs1394810940 Functional Loss SNV dbSNP153 33..33 33 - - - 59216 RMVar_ID_59216 Human_SNP_ID_705906523 m1A Human chr22 + 46293809 46293809 46293809 GAATGTGCCGCTGACTCAGCTGTGCTGCTTTCAGCCCTCCTGTGAGGGGCGGTCCCAGTGCACAG GAATGTGCCGCTGACTCAGCTGTGCTGCTTTCGGCCCTCCTGTGAGGGGCGGTCCCAGTGCACAG A G TTC38 Ensembl:ENSG00000075234 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:46293759..46293958 32194978 MeRIP-seq:(Medium) rs1406616856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582880 Human_miRNA_ID_1408033,Human_miRNA_ID_2701958,Human_miRNA_ID_2778676 RMVar_hsa_circ_87203,RMVar_hsa_circ_215072,RMVar_hsa_circ_103456,RMVar_hsa_circ_215074,RMVar_hsa_circ_110881,RMVar_hsa_circ_215078 59217 RMVar_ID_59217 Human_SNP_ID_705910508 m1A Human chr22 + 46308564 46308564 46308564 GAACCAGGCAGCCCAAGCTGCCAAGCCTGAAGACCCTCGGAGCCAGGGCGTGGAAAGATTCATAC GAACCAGGCAGCCCAAGCTGCCAAGCCTGAAGGCCCTCGGAGCCAGGGCGTGGAAAGATTCATAC A G GTSE1 Ensembl:ENSG00000075218 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46308452..46308819 26863196 MeRIP-seq:(Medium) rs762028294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931179,Human_RBP_ID_4704837,Human_RBP_ID_26346077,Human_RBP_ID_27310099,Human_RBP_ID_27495487,Human_RBP_ID_27821386 RMVar_hsa_circ_6108,RMVar_hsa_circ_344587,RMVar_hsa_circ_25509,RMVar_hsa_circ_215081,RMVar_hsa_circ_348454,RMVar_hsa_circ_336903,RMVar_hsa_circ_341430,RMVar_hsa_circ_316784,RMVar_hsa_circ_34265,RMVar_hsa_circ_215082 59218 RMVar_ID_59218 Human_SNP_ID_705913044 m1A Human chr22 + 46317819 46317819 46317819 GCCCGCGAGACCCCTGCACTCCTGCTGCTGCAAGATGACACCTTCTCGGCCCTGTGAGCTCCGCT GCCCGCGAGACCCCTGCACTCCTGCTGCTGCAGGATGACACCTTCTCGGCCCTGTGAGCTCCGCT A G GTSE1 Ensembl:ENSG00000075218 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:46317738..46317907 26863196 MeRIP-seq:(Medium) rs1197537321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14522915 RMVar_hsa_circ_344587,RMVar_hsa_circ_25509,RMVar_hsa_circ_215081,RMVar_hsa_circ_341430,RMVar_hsa_circ_215083,RMVar_hsa_circ_327277,RMVar_hsa_circ_19640,RMVar_hsa_circ_215085,RMVar_hsa_circ_94638,RMVar_hsa_circ_215086,RMVar_hsa_circ_284565 59219 RMVar_ID_59219 Human_SNP_ID_705913216 m1A Human chr22 - 46318613 46318613 46318613 ACCGGCTGCCTCAGTCTCCTGGTTCAGATCTCAGTCCCGTGTCACCTCCTGACCATCTTTGCCAA ACCGGCTGCCTCAGTCTCCTGGTTCAGATCTCCGTCCCGTGTCACCTCCTGACCATCTTTGCCAA T G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46318521..46318856 26863196 MeRIP-seq:(Medium) rs28522526 Functional Loss SNV dbSNP153 33..33 33 - - - 59220 RMVar_ID_59220 Human_SNP_ID_705913490 m1A Human chr22 - 46319504 46319504 46319504 GCCTCTTCCAGCCCTCCTGTCACATGAGTGGCAGCACCCAGGTTCCGCCAGAACCTCAGGGACAC GCCTCTTCCAGCCCTCCTGTCACATGAGTGGCGGCACCCAGGTTCCGCCAGAACCTCAGGGACAC T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46319500..46319584 26863196 MeRIP-seq:(Medium) rs1380201567 Functional Loss SNV dbSNP153 33..33 33 - - - 59221 RMVar_ID_59221 Human_SNP_ID_705916627 m1A Human chr22 - 46330373 46330373 46330373 AGCTCAGGCCATCCTCCCACTTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGCACTACCACAC AGCTCAGGCCATCCTCCCACTTCAGCCTCCCAGGTAGCTGGGACTACAGGCATGCACTACCACAC T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46330322..46330422 26863196 MeRIP-seq:(Medium) rs1215354212 Functional Loss SNV dbSNP153 33..33 33 - - - 59222 RMVar_ID_59222 Human_SNP_ID_705918097 m1A Human chr22 - 46335775 46335775 46335775 CGCCGCCGGACAGGGCGCACACGACGTGCCGCAAGGCCTGCATCCGCCAGTCGCCCAACTTCGCC CGCCGCCGGACAGGGCGCACACGACGTGCCGCGAGGCCTGCATCCGCCAGTCGCCCAACTTCGCC T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:46335726..46335891;chr22:46335726..46335881;chr22:46335726..46335900;chr22:46335726..46335918 26863196 MeRIP-seq:(Medium) rs1353951169 Functional Loss SNV dbSNP153 33..33 33 - - - 59223 RMVar_ID_59223 Human_SNP_ID_705918128 m1A Human chr22 - 46335808 46335808 46335808 GCCTCAGCAGCAGCGCGGCCACGGCGCTGTCCACGCCGCCGGACAGGGCGCACACGACGTGCCGC GCCTCAGCAGCAGCGCGGCCACGGCGCTGTCCCCGCCGCCGGACAGGGCGCACACGACGTGCCGC T G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:46335757..46335908 26863196 MeRIP-seq:(Medium) rs1264204669 Functional Loss SNV dbSNP153 33..33 33 - - - 59224 RMVar_ID_59224 Human_SNP_ID_705922594 m1A Human chr22 - 46351058 46351034 46351059 TTTGGCATCTCCATTCCCTACTCTCAGACCCCACTGGTGCTTCCCACCCAGGGTCCTACACCTCC TTTGGCATCTCCATTCCCTACTCTCAGACCC_________________________TACACCTCC AGGACCCTGGGTGGGAAGCACCAGTG A lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46351034..46351262 26863196 MeRIP-seq:(Medium) rs1432883329 Functional Loss DEL dbSNP153 32..56 33 - - - 59225 RMVar_ID_59225 Human_SNP_ID_705923295 m1A Human chr22 - 46352789 46352788 46352789 CAGCACAGGCTCACGCAGGCCTCACCGCAGTAAGGGTCTGCACATGAGCGAGCAGCACTCTGGCC CAGCACAGGCTCACGCAGGCCTCACCGCAGTA_GGGTCTGCACATGAGCGAGCAGCACTCTGGCC CT C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46352752..46353074 26863196 MeRIP-seq:(Medium) rs952512627 Functional Loss DEL dbSNP153 33..33 33 - - - 59226 RMVar_ID_59226 Human_SNP_ID_705923687 m1A Human chr22 - 46353866 46353866 46353866 CCAGTGCTGTCTCAGAGGCCGGCCCACTCACCACAAACACGTCACCCTTGACGCTGTCCTTCTCC CCAGTGCTGTCTCAGAGGCCGGCCCACTCACCGCAAACACGTCACCCTTGACGCTGTCCTTCTCC T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46353828..46353911 26863196 MeRIP-seq:(Medium) rs1466804790 Functional Loss SNV dbSNP153 33..33 33 - - - 59227 RMVar_ID_59227 Human_SNP_ID_705924691 m1A Human chr22 - 46356369 46356369 46356369 CACAGGGGCCCCGACCCTCTGCCTCTTTGAGCACTGTCCTCATGCCCCTTCCATTTTCTGTCCTC CACAGGGGCCCCGACCCTCTGCCTCTTTGAGCCCTGTCCTCATGCCCCTTCCATTTTCTGTCCTC T G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46355917..46356541 26863196 MeRIP-seq:(Medium) rs979555991 Functional Loss SNV dbSNP153 33..33 33 - - - 59228 RMVar_ID_59228 Human_SNP_ID_705924693 m1A Human chr22 - 46356372 46356372 46356372 GCCCACAGGGGCCCCGACCCTCTGCCTCTTTGAGCACTGTCCTCATGCCCCTTCCATTTTCTGTC GCCCACAGGGGCCCCGACCCTCTGCCTCTTTGCGCACTGTCCTCATGCCCCTTCCATTTTCTGTC T G lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46356338..46356472 26863196 MeRIP-seq:(Medium) rs571961106 Functional Loss SNV dbSNP153 33..33 33 - - - 59229 RMVar_ID_59229 Human_SNP_ID_705924695 m1A Human chr22 + 46356382 46356382 46356382 GGAAGGGGCATGAGGACAGTGCTCAAAGAGGCAGAGGGTCGGGGCCCCTGTGGGCCGAGTGTGCA GGAAGGGGCATGAGGACAGTGCTCAAAGAGGCGGAGGGTCGGGGCCCCTGTGGGCCGAGTGTGCA A G TRMU Ensembl:ENSG00000100416 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46355941..46356495 26863196 MeRIP-seq:(Medium) rs1379712511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5389564,Human_RBP_ID_14523511 59230 RMVar_ID_59230 Human_SNP_ID_705927424 m1A Human chr22 + 46364130 46364130 46364130 ATGGCGCAGTCGGGGCCGCCAGAGCCCAGGGAAGACGTGCGCGAGGATGTGGGGCTCTGCTCACA ATGGCGCAGTCGGGGCCGCCAGAGCCCAGGGAGGACGTGCGCGAGGATGTGGGGCTCTGCTCACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46364079..46364177 26863196 MeRIP-seq:(Medium) rs1280822264 Functional Loss SNV dbSNP153 33..33 33 - - - 59231 RMVar_ID_59231 Human_SNP_ID_705927494 m1A Human chr22 + 46364233 46364233 46364233 GCTCCGTCAGCGTCAGCGGCGGCGGGTAGGTGACTTTATTTTTCAAGATGCCTGGGAGGAGGAGA GCTCCGTCAGCGTCAGCGGCGGCGGGTAGGTGCCTTTATTTTTCAAGATGCCTGGGAGGAGGAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46364086..46364275 26863196 MeRIP-seq:(Medium) rs368331702 Functional Loss SNV dbSNP153 33..33 33 - - - 59232 RMVar_ID_59232 Human_SNP_ID_705930639 m1A Human chr22 + 46371705 46371702 46371706 AACCATCCTATTCATATCCACTGACTTATCCCATCCATCCATCTACCCACCCATCCATCCACTCA AACCATCCTATTCATATCCACTGACTTATC____CCATCCATCTACCCACCCATCCATCCACTCA CCCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46371518..46372470 26863196 MeRIP-seq:(Medium) rs1390569712 Functional Loss DEL dbSNP153 31..34 33 - - - 59233 RMVar_ID_59233 Human_SNP_ID_705930666 m1A Human chr22 + 46371786 46371783 46371787 TCCATCCACCTATTCATCCACTCACATATCCCATCCATCCACCCACCCATCCATCCACTCACTCA TCCATCCACCTATTCATCCACTCACATATC____CCATCCACCCACCCATCCATCCACTCACTCA CCCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46371510..46371891 26863196 MeRIP-seq:(Medium) rs1469130342 Functional Loss DEL dbSNP153 31..34 33 - - - 59234 RMVar_ID_59234 Human_SNP_ID_705930681 m1A Human chr22 + 46371826 46371826 46371826 ACCCACCCATCCATCCACTCACTCATCTCTCCATCCCTCCATCCATCCACCTATTCATCCACTCA ACCCACCCATCCATCCACTCACTCATCTCTCCGTCCCTCCATCCATCCACCTATTCATCCACTCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46371743..46371849 26863196 MeRIP-seq:(Medium) rs549430300 Functional Loss SNV dbSNP153 33..33 33 - - - 59235 RMVar_ID_59235 Human_SNP_ID_705930754 m1A Human chr22 - 46371996 46371996 46371996 GAGTAGATGGGTGAATAGATGGATGAGTGGGTAGCTGGATGGATGGAGGAGTGAGTTGAGTGGAT GAGTAGATGGGTGAATAGATGGATGAGTGGGTGGCTGGATGGATGGAGGAGTGAGTTGAGTGGAT T C CELSR1 Ensembl:ENSG00000075275 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46371956..46372055 26863196 MeRIP-seq:(Medium) rs1016443442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117485,RMVar_hsa_circ_85956,RMVar_hsa_circ_215093,RMVar_hsa_circ_127246,RMVar_hsa_circ_111345,RMVar_hsa_circ_112741,RMVar_hsa_circ_215094,RMVar_hsa_circ_121610,RMVar_hsa_circ_215095,RMVar_hsa_circ_215096,RMVar_hsa_circ_94973,RMVar_hsa_circ_215097,RMVar_hsa_circ_215098,RMVar_hsa_circ_215099 59236 RMVar_ID_59236 Human_SNP_ID_705932063 m1A Human chr22 + 46375290 46375290 46375290 GGCTCATGCGCCACACCTTCCTTGGCCTCTGCAGGTGTCCCATCTCACCCAGACCCTGCCTCTCA GGCTCATGCGCCACACCTTCCTTGGCCTCTGCGGGTGTCCCATCTCACCCAGACCCTGCCTCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46375288..46375487 26863196 MeRIP-seq:(Medium) rs1456771023 Functional Loss SNV dbSNP153 33..33 33 - - - 59237 RMVar_ID_59237 Human_SNP_ID_705946550 m1A Human chr22 + 46419973 46419973 46419973 TCATGCACACTCACCCACGCACACGTGCACTCACCCTTATGTACACTCACCCACAATCATGTGCA TCATGCACACTCACCCACGCACACGTGCACTCGCCCTTATGTACACTCACCCACAATCATGTGCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:46419851..46420221 26863196 MeRIP-seq:(Medium) rs924118930 Functional Loss SNV dbSNP153 33..33 33 - - - 59238 RMVar_ID_59238 Human_SNP_ID_705946658 m1A Human chr22 + 46420220 46420218 46420220 ATGTGCACACCTACCCACACTCGTACATACCCACATTCACACCCACATATGCTCACCCACACTCA ATGTGCACACCTACCCACACTCGTACATACC__CATTCACACCCACATATGCTCACCCACACTCA CCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46419891..46420386 26863196 MeRIP-seq:(Medium) rs1371364894 Functional Loss DEL dbSNP153 32..33 33 - - - 59239 RMVar_ID_59239 Human_SNP_ID_705946724 m1A Human chr22 - 46420341 46420339 46420341 GGGTGAGCATGCACATGTGGGTAAATGTGCACATGAGTGCACGAGTGGGTGAGTGCATACGTGAG GGGTGAGCATGCACATGTGGGTAAATGTGCAC__GAGTGCACGAGTGGGTGAGTGCATACGTGAG CAT C CELSR1 Ensembl:ENSG00000075275 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46420336..46420510 26863196 MeRIP-seq:(Medium) rs566991196 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117485,RMVar_hsa_circ_85956,RMVar_hsa_circ_111345,RMVar_hsa_circ_215094,RMVar_hsa_circ_121610,RMVar_hsa_circ_215096,RMVar_hsa_circ_94973,RMVar_hsa_circ_215097,RMVar_hsa_circ_215098,RMVar_hsa_circ_125686,RMVar_hsa_circ_123298,RMVar_hsa_circ_215099,RMVar_hsa_circ_215100,RMVar_hsa_circ_215102,RMVar_hsa_circ_81255,RMVar_hsa_circ_36493,RMVar_hsa_circ_215103,RMVar_hsa_circ_215110,RMVar_hsa_circ_115179,RMVar_hsa_circ_215112,RMVar_hsa_circ_124327,RMVar_hsa_circ_120591,RMVar_hsa_circ_87343,RMVar_hsa_circ_116547,RMVar_hsa_circ_215113,RMVar_hsa_circ_114676,RMVar_hsa_circ_215114,RMVar_hsa_circ_215115,RMVar_hsa_circ_280983,RMVar_hsa_circ_215117 59240 RMVar_ID_59240 Human_SNP_ID_705960303 m1A Human chr22 - 46463865 46463865 46463865 CAGCTCCACCACCGTGCTCTTCCGGCCCATCCACCCCATCAACGGCCTGCGCTGCCGCTGCCCGC CAGCTCCACCACCGTGCTCTTCCGGCCCATCCTCCCCATCAACGGCCTGCGCTGCCGCTGCCCGC T A CELSR1 Ensembl:ENSG00000075275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46463823..46463922 26863196 MeRIP-seq:(Medium) rs1489471148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17988530,Human_RBP_ID_27495542 RMVar_hsa_circ_112421,RMVar_hsa_circ_89790,RMVar_hsa_circ_215120,RMVar_hsa_circ_343085,RMVar_hsa_circ_215121,RMVar_hsa_circ_215122 59241 RMVar_ID_59241 Human_SNP_ID_705981843 m1A Human chr22 - 46535876 46535876 46535876 CGAGTACCAGCTCCTGGTGGAGGCCAACGACCAGGGGCGCAATCCGGGCCCGCTCAGTGCCACGG CGAGTACCAGCTCCTGGTGGAGGCCAACGACCGGGGGCGCAATCCGGGCCCGCTCAGTGCCACGG T C CELSR1 Ensembl:ENSG00000075275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46535826..46535979 26863196 MeRIP-seq:(Medium) rs1336968290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2437464 RMVar_hsa_circ_112421,RMVar_hsa_circ_89790,RMVar_hsa_circ_215120,RMVar_hsa_circ_215122 59242 RMVar_ID_59242 Human_SNP_ID_705982529 m1A Human chr22 - 46537313 46537313 46537313 AGGCCGGGCGCGTGGTCCCCACAGTCCCCGCCAGGGCCCCCGGGGAGGCGGGACGCGGACCGCCC AGGCCGGGCGCGTGGTCCCCACAGTCCCCGCCTGGGCCCCCGGGGAGGCGGGACGCGGACCGCCC T A CELSR1 Ensembl:ENSG00000075275 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46537267..46537487 26863196 MeRIP-seq:(Medium) rs1363546358 Functional Loss SNV dbSNP153 33..33 33 - - - 59243 RMVar_ID_59243 Human_SNP_ID_705993897 m1A Human chr22 + 46577240 46577240 46577240 GCGGCAGGCGTAGCGCGGCCGGGCGGCCGGCGAGGGGGGCGCCGCGGCGGGTGGATGAGAGTTGG GCGGCAGGCGTAGCGCGGCCGGGCGGCCGGCGGGGGGGGCGCCGCGGCGGGTGGATGAGAGTTGG A G GRAMD4 Ensembl:ENSG00000075240 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46577140..46577332 26863196 MeRIP-seq:(Medium) rs1315593126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676881,Human_RBP_ID_4708310,Human_RBP_ID_5324854,Human_RBP_ID_8729530,Human_RBP_ID_9332918 Human_Splice_Rec_2176647 59244 RMVar_ID_59244 Human_SNP_ID_705993906 m1A Human chr22 - 46577259 46577259 46577259 CCCTGAGCGGATATCGGGGCCAACTCTCATCCACCCGCCGCGGCGCCCCCCTCGCCGGCCGCCCG CCCTGAGCGGATATCGGGGCCAACTCTCATCCCCCCGCCGCGGCGCCCCCCTCGCCGGCCGCCCG T G lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:46577130..46577268 26863410 MeRIP-seq:(Medium) rs1026963271 Functional Loss SNV dbSNP153 33..33 33 - - - 59245 RMVar_ID_59245 Human_SNP_ID_705997113 m1A Human chr22 - 46587852 46587850 46587853 CGGCCCCACCCCGACGCCCGGGCTTCTGGCGCACACGCCTGTTTCACTTCCTCTCCACCAAACAT CGGCCCCACCCCGACGCCCGGGCTTCTGGCG___ACGCCTGTTTCACTTCCTCTCCACCAAACAT TGTG T lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46587841..46587962 26863196 MeRIP-seq:(Medium) rs533797227 Functional Loss DEL dbSNP153 32..34 33 - - - 59246 RMVar_ID_59246 Human_SNP_ID_705997964 m1A Human chr22 + 46590643 46590641 46590643 GCTGGGCCCAGGTGAGTGTCAACAGGGGAGGGAGAGAGCAGCAGAGGTCCCGCCAGGGCGTGCTT GCTGGGCCCAGGTGAGTGTCAACAGGGGAGG__GAGAGCAGCAGAGGTCCCGCCAGGGCGTGCTT GGA G GRAMD4 Ensembl:ENSG00000075240 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46590639..46590704 26863196 MeRIP-seq:(Medium) rs1418620355 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_266043,Human_RBP_ID_3676901,Human_RBP_ID_8207452,Human_RBP_ID_9433871,Human_RBP_ID_18464013,Human_RBP_ID_22418104,Human_RBP_ID_22479861,Human_RBP_ID_26789934 59247 RMVar_ID_59247 Human_SNP_ID_706017479 m1A Human chr22 + 46652207 46652207 46652207 GATGGTTCTGGATTATCTGGGGGCGCACAGTCACCACAAAGGTTCTGAGAAGGAGATGGCAGGAA GATGGTTCTGGATTATCTGGGGGCGCACAGTCGCCACAAAGGTTCTGAGAAGGAGATGGCAGGAA A G GRAMD4 Ensembl:ENSG00000075240 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46652199..46652411 26863196 MeRIP-seq:(Medium) rs186572859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97880,RMVar_hsa_circ_117590,RMVar_hsa_circ_373627,RMVar_hsa_circ_113977,RMVar_hsa_circ_215124,RMVar_hsa_circ_93724,RMVar_hsa_circ_215126,RMVar_hsa_circ_215127,RMVar_hsa_circ_215125,RMVar_hsa_circ_98892,RMVar_hsa_circ_215123,RMVar_hsa_circ_215129,RMVar_hsa_circ_49695 59248 RMVar_ID_59248 Human_SNP_ID_706019199 m1A Human chr22 + 46658277 46658277 46658277 GGACCGCGAGCGGCAGCGGCGGATGGAGCTGGAGCAGAAGGTGCAGGAGGTGCTGAAGGCCAGGT GGACCGCGAGCGGCAGCGGCGGATGGAGCTGGGGCAGAAGGTGCAGGAGGTGCTGAAGGCCAGGT A G GRAMD4 Ensembl:ENSG00000075240 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46658226..46658338 26863196 MeRIP-seq:(Medium) rs1023168833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929596,Human_RBP_ID_3963389,Human_RBP_ID_9393127,Human_RBP_ID_19009450,Human_RBP_ID_26346079,Human_RBP_ID_27821745 Human_Splice_Rec_2176654,Human_Splice_Rec_2176655,Human_Splice_Rec_2176688,Human_Splice_Rec_2176689 RMVar_hsa_circ_13768,RMVar_hsa_circ_97880,RMVar_hsa_circ_117590,RMVar_hsa_circ_373627,RMVar_hsa_circ_113977,RMVar_hsa_circ_215124,RMVar_hsa_circ_93724,RMVar_hsa_circ_215126,RMVar_hsa_circ_215127,RMVar_hsa_circ_215125,RMVar_hsa_circ_98892,RMVar_hsa_circ_215123,RMVar_hsa_circ_215129,RMVar_hsa_circ_49695,RMVar_hsa_circ_353049 59249 RMVar_ID_59249 Human_SNP_ID_706019203 m1A Human chr22 + 46658289 46658289 46658289 GCAGCGGCGGATGGAGCTGGAGCAGAAGGTGCAGGAGGTGCTGAAGGCCAGGTACCGCGCCTTCC GCAGCGGCGGATGGAGCTGGAGCAGAAGGTGCGGGAGGTGCTGAAGGCCAGGTACCGCGCCTTCC A G GRAMD4 Ensembl:ENSG00000075240 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46658239..46658345 26863196 MeRIP-seq:(Medium) rs556143177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929596,Human_RBP_ID_3963389,Human_RBP_ID_9393127,Human_RBP_ID_19009450,Human_RBP_ID_26346079,Human_RBP_ID_27821745 Human_Splice_Rec_2176655,Human_Splice_Rec_2176689 RMVar_hsa_circ_13768,RMVar_hsa_circ_97880,RMVar_hsa_circ_117590,RMVar_hsa_circ_373627,RMVar_hsa_circ_113977,RMVar_hsa_circ_215124,RMVar_hsa_circ_93724,RMVar_hsa_circ_215126,RMVar_hsa_circ_215127,RMVar_hsa_circ_215125,RMVar_hsa_circ_98892,RMVar_hsa_circ_215123,RMVar_hsa_circ_215129,RMVar_hsa_circ_49695,RMVar_hsa_circ_353049 59250 RMVar_ID_59250 Human_SNP_ID_706023529 m1A Human chr22 - 46672176 46672176 46672176 GGCCTGACTGCGCCCCAGGACCCCACCTGGCAACAGATGCAGGGATGGGAGGCGGGGCCGGCCCC GGCCTGACTGCGCCCCAGGACCCCACCTGGCATCAGATGCAGGGATGGGAGGCGGGGCCGGCCCC T A lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46672174..46672278 26863196 MeRIP-seq:(Medium) rs1054905139 Functional Loss SNV dbSNP153 33..33 33 - - - 59251 RMVar_ID_59251 Human_SNP_ID_706025116 m1A Human chr22 - 46676851 46676851 46676851 CCTGTCTGTCCGGTGACTCGATGGCCCCAGCAAGATTTCCAACCCAACCTGGACGCAGCCCCAGG CCTGTCTGTCCGGTGACTCGATGGCCCCAGCAGGATTTCCAACCCAACCTGGACGCAGCCCCAGG T C lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46676809..46676887 26863196 MeRIP-seq:(Medium) rs916485099 Functional Loss SNV dbSNP153 33..33 33 - - - 59252 RMVar_ID_59252 Human_SNP_ID_706037890 m1A Human chr22 + 46720152 46720152 46720152 CCACAAGTGACACAGCTGCTCCTCTGGACACCAGAAAGTCACCTGCGCCCACTTCCAGCGGTGCC CCACAAGTGACACAGCTGCTCCTCTGGACACCGGAAAGTCACCTGCGCCCACTTCCAGCGGTGCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:46720101..46720225 32194978 MeRIP-seq:(Medium) rs375439966 Functional Loss SNV dbSNP153 33..33 33 - - - 59253 RMVar_ID_59253 Human_SNP_ID_706043027 m1A Human chr22 - 46738226 46738226 46738226 CCTCCCGCCGCCCGCCGCCCGCCGCCCGGGCCACTGCAGGGGCCGCTAACGGTCCGGCGCCCCTC CCTCCCGCCGCCCGCCGCCCGCCGCCCGGGCCCCTGCAGGGGCCGCTAACGGTCCGGCGCCCCTC T G CERK Ensembl:ENSG00000100422 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:46738140..46738235 26863410 MeRIP-seq:(Medium) rs1569333822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268955,RMVar_hsa_circ_127219,RMVar_hsa_circ_215145 59254 RMVar_ID_59254 Human_SNP_ID_706049482 m1A Human chr22 - 46762158 46762155 46762159 ATAACCGCGGAGCGTATTCGAAGAGATGAGAGAGACTGGGGATTAGGCCAGGCTTGAAGGGAAGA ATAACCGCGGAGCGTATTCGAAGAGATGAGA____CTGGGGATTAGGCCAGGCTTGAAGGGAAGA GTCTC G AL118516.1 Ensembl:ENSG00000260708 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:46762036..46762372 32194978 MeRIP-seq:(Medium) rs376977048 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_1136757,Human_RBP_ID_1614278,Human_RBP_ID_3679507,Human_RBP_ID_5601424,Human_RBP_ID_23953289 59255 RMVar_ID_59255 Human_SNP_ID_706049555 m1A Human chr22 + 46762414 46762414 46762414 GGGGCAGTTCAGCTTTGGAAATGAGGAGCTCGAGGCTCCTGGGAGTCCGTTGCGGGCAGGTGGGC GGGGCAGTTCAGCTTTGGAAATGAGGAGCTCGCGGCTCCTGGGAGTCCGTTGCGGGCAGGTGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:46762366..46762502 26863196 MeRIP-seq:(Medium) rs1266535337 Functional Loss SNV dbSNP153 33..33 33 - - - 59256 RMVar_ID_59256 Human_SNP_ID_706053778 m1A Human chr22 + 46776128 46776128 46776128 AAGCCCTGTGGCAGTATAGGCAAGGAAAGGGGAGTTTTCACTGAGGACATGAGATGACATTAAAG AAGCCCTGTGGCAGTATAGGCAAGGAAAGGGGGGTTTTCACTGAGGACATGAGATGACATTAAAG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46776122..46776766 26863196 MeRIP-seq:(Medium) rs1189228490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14524517 RMVar_hsa_circ_81448,RMVar_hsa_circ_215148 59257 RMVar_ID_59257 Human_SNP_ID_706074456 m1A Human chr22 - 46854092 46854092 46854092 TGCGGAAAGACAGGCAGAGTCCCAACCAAGGAAGAGCGTGTTTAAAACAAGAAGTCCAGAAACGC TGCGGAAAGACAGGCAGAGTCCCAACCAAGGAGGAGCGTGTTTAAAACAAGAAGTCCAGAAACGC T C RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:46854007..46854120 26863196 MeRIP-seq:(Medium) rs1038758796 Functional Loss SNV dbSNP153 33..33 33 - - - 59258 RMVar_ID_59258 Human_SNP_ID_706082340 m1A Human chr22 + 46884140 46884140 46884140 CATTTTGGTGGGAGAAGACAAACAATACACCGAGAAGTAGATTTGATGTGCTGTGGAATGTGAGG CATTTTGGTGGGAGAAGACAAACAATACACCGTGAAGTAGATTTGATGTGCTGTGGAATGTGAGG A T TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46884126..46884305 26863196 MeRIP-seq:(Medium) rs1167086014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8138,RMVar_hsa_circ_333121,RMVar_hsa_circ_331055,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449,RMVar_hsa_circ_286588,RMVar_hsa_circ_311676,RMVar_hsa_circ_365488,RMVar_hsa_circ_361689,RMVar_hsa_circ_300395,RMVar_hsa_circ_215154,RMVar_hsa_circ_271787,RMVar_hsa_circ_215153 59259 RMVar_ID_59259 Human_SNP_ID_706082532 m1A Human chr22 + 46884848 46884848 46884848 CACTGAGGCAGGAGAGGTGTGGCATTTAAGGAACATTTAAGCAGCGAAGTAAAAGTGGGAGGGGC CACTGAGGCAGGAGAGGTGTGGCATTTAAGGAGCATTTAAGCAGCGAAGTAAAAGTGGGAGGGGC A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46884847..46884960 26863196 MeRIP-seq:(Medium) rs923945732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8138,RMVar_hsa_circ_333121,RMVar_hsa_circ_331055,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449,RMVar_hsa_circ_286588,RMVar_hsa_circ_311676,RMVar_hsa_circ_365488,RMVar_hsa_circ_361689,RMVar_hsa_circ_300395,RMVar_hsa_circ_215154,RMVar_hsa_circ_271787,RMVar_hsa_circ_215153 59260 RMVar_ID_59260 Human_SNP_ID_706091527 m1A Human chr22 + 46915020 46915020 46915020 GGCTAGATTGAGGCCGGGCATTCAGAGAGGGCAGCAGAAGGGCCGGCCTGGAATCCAAGGTGCAG GGCTAGATTGAGGCCGGGCATTCAGAGAGGGCGGCAGAAGGGCCGGCCTGGAATCCAAGGTGCAG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:46914975..46915092 26863196 MeRIP-seq:(Medium) rs1031520475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134,RMVar_hsa_circ_331055,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449,RMVar_hsa_circ_113538,RMVar_hsa_circ_311676,RMVar_hsa_circ_361689,RMVar_hsa_circ_300395,RMVar_hsa_circ_19320,RMVar_hsa_circ_8342,RMVar_hsa_circ_215156,RMVar_hsa_circ_215155,RMVar_hsa_circ_215160,RMVar_hsa_circ_97358,RMVar_hsa_circ_303210,RMVar_hsa_circ_314060,RMVar_hsa_circ_265114 59261 RMVar_ID_59261 Human_SNP_ID_706114211 m1A Human chr22 + 46997676 46997676 46997676 CCTTTGCCCAACCTGGGATTCAAATGAAAGTGAAAATGTTAGAAGAACTCGTGAGCCGGATTGAT CCTTTGCCCAACCTGGGATTCAAATGAAAGTGGAAATGTTAGAAGAACTCGTGAGCCGGATTGAT A G TBC1D22A Ensembl:ENSG00000054611 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:46997626..46997675 32194978 MeRIP-seq:(Medium) rs775814845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931201,Human_RBP_ID_1944590,Human_RBP_ID_5601751,Human_RBP_ID_19009472,Human_RBP_ID_27821389 Human_Splice_Rec_2176816,Human_Splice_Rec_2176817,Human_Splice_Rec_2176840,Human_Splice_Rec_2176841,Human_Splice_Rec_2176874,Human_Splice_Rec_2176875,Human_Splice_Rec_2176894,Human_Splice_Rec_2176895,Human_Splice_Rec_2176916,Human_Splice_Rec_2176917,Human_Splice_Rec_2176956,Human_Splice_Rec_2176957,Human_Splice_Rec_2176980,Human_Splice_Rec_2176981 RMVar_hsa_circ_134,RMVar_hsa_circ_331055,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449,RMVar_hsa_circ_113538,RMVar_hsa_circ_311676,RMVar_hsa_circ_300395,RMVar_hsa_circ_19320,RMVar_hsa_circ_215163,RMVar_hsa_circ_215155,RMVar_hsa_circ_215160,RMVar_hsa_circ_97358,RMVar_hsa_circ_303210,RMVar_hsa_circ_314060,RMVar_hsa_circ_265114,RMVar_hsa_circ_278708,RMVar_hsa_circ_215162,RMVar_hsa_circ_309940,RMVar_hsa_circ_274333,RMVar_hsa_circ_215165,RMVar_hsa_circ_215164,RMVar_hsa_circ_215169,RMVar_hsa_circ_364631,RMVar_hsa_circ_215168,RMVar_hsa_circ_282986 59262 RMVar_ID_59262 Human_SNP_ID_706132996 m1A Human chr22 + 47062978 47062978 47062978 GGGAAAAAGCCTGAAGGTGAGAAACAGCAGCGAGCGCAGGAACATGGAAACAGGGAGAAGGTGCC GGGAAAAAGCCTGAAGGTGAGAAACAGCAGCGGGCGCAGGAACATGGAAACAGGGAGAAGGTGCC A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:47062973..47063109 26863196 MeRIP-seq:(Medium) rs1028941810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331055,RMVar_hsa_circ_113538,RMVar_hsa_circ_215163,RMVar_hsa_circ_215155,RMVar_hsa_circ_265114,RMVar_hsa_circ_309940,RMVar_hsa_circ_364631,RMVar_hsa_circ_336047,RMVar_hsa_circ_215171 59263 RMVar_ID_59263 Human_SNP_ID_706147912 m1A Human chr22 + 47114388 47114388 47114388 GAGGAGCCATGAGATTGATTTTCTTCCTTTAGAGGAAGAGGAAGTTGGTTCTTTGATGCCATAGG GAGGAGCCATGAGATTGATTTTCTTCCTTTAGGGGAAGAGGAAGTTGGTTCTTTGATGCCATAGG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:47114385..47114553 26863196 MeRIP-seq:(Medium) rs921227844 Functional Loss SNV dbSNP153 33..33 33 - - - 59264 RMVar_ID_59264 Human_SNP_ID_706147932 m1A Human chr22 - 47114440 47114439 47114441 ACAGCATTCTCTCCATCCAACCCCTCACTCACAGCATTCTCTCCATCCAACCCCTATGGCATCAA ACAGCATTCTCTCCATCCAACCCCTCACTCA__GCATTCTCTCCATCCAACCCCTATGGCATCAA CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:47114430..47114584 26863196 MeRIP-seq:(Medium) rs1289221424 Functional Loss DEL dbSNP153 32..33 33 - - - 59265 RMVar_ID_59265 Human_SNP_ID_706159479 m1A Human chr22 + 47153585 47153585 47153585 AGGAGGCGGCCATGCAGGTGGACGGGCAAGGGAAAAGGGAGGAGCTGTGGCCGTCGTGCAAGCGA AGGAGGCGGCCATGCAGGTGGACGGGCAAGGGCAAAGGGAGGAGCTGTGGCCGTCGTGCAAGCGA A C TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:47153575..47153773 26863196 MeRIP-seq:(Medium) rs1386845694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_209491,Human_RBP_ID_265484,Human_RBP_ID_1068951,Human_RBP_ID_3677056,Human_RBP_ID_5203768,Human_RBP_ID_8207542,Human_RBP_ID_26789949 59266 RMVar_ID_59266 Human_SNP_ID_706165899 m1A Human chr22 + 47173601 47173601 47173601 CGAGGCCTACCGCCTCAAGTTTGCTTTTGCCGACGCCCCCAATCACTACAAGAAATGAGCCCAGG CGAGGCCTACCGCCTCAAGTTTGCTTTTGCCGGCGCCCCCAATCACTACAAGAAATGAGCCCAGG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:47173557..47173683 26863196 MeRIP-seq:(Medium) rs763586138 Functional Loss SNV dbSNP153 33..33 33 - - - 59267 RMVar_ID_59267 Human_SNP_ID_706165905 m1A Human chr22 + 47173610 47173610 47173610 CCGCCTCAAGTTTGCTTTTGCCGACGCCCCCAATCACTACAAGAAATGAGCCCAGGCCCACCCGC CCGCCTCAAGTTTGCTTTTGCCGACGCCCCCAGTCACTACAAGAAATGAGCCCAGGCCCACCCGC A G TBC1D22A Ensembl:ENSG00000054611 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:47173559..47173700 26863196 MeRIP-seq:(Medium) rs752962513 Functional Loss SNV dbSNP153 33..33 33 - - - 59268 RMVar_ID_59268 Human_SNP_ID_706226707 m1A Human chr22 + 47379320 47379320 47379320 GGAGGAGGCGGAGGCGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGG GGAGGAGGCGGAGGCGGAGGCGGCGGCGGAGGCGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:47379275..47379386 26863196 MeRIP-seq:(Medium) rs867314270 Functional Loss SNV dbSNP153 33..33 33 - - - 59269 RMVar_ID_59269 Human_SNP_ID_706226714 m1A Human chr22 + 47379332 47379323 47379332 GGCGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGG GGCGGAGGCGGCGGCGGAGGAGGC_________GGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGG CGGCGGCGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:47379285..47379384 26863196 MeRIP-seq:(Medium) rs1569017102 Functional Loss DEL dbSNP153 25..33 33 - - - 59270 RMVar_ID_59270 Human_SNP_ID_706226715 m1A Human chr22 + 47379335 47379323 47379335 GGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGGAGG GGAGGCGGCGGCGGAGGAGGC____________GGCGGCGGCGGAGGAGGCGGCGGCGGCGGAGG CGGCGGCGGAGGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:47379256..47379389 26863196 MeRIP-seq:(Medium) rs1569017105 Functional Loss DEL dbSNP153 22..33 33 - - - 59271 RMVar_ID_59271 Human_SNP_ID_706226729 m1A Human chr22 + 47379332 47379332 47379332 GGCGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGG GGCGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:47379285..47379384 26863196 MeRIP-seq:(Medium) rs939494623 Functional Loss SNV dbSNP153 33..33 33 - - - 59272 RMVar_ID_59272 Human_SNP_ID_706226732 m1A Human chr22 + 47379335 47379335 47379335 GGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGAGGCGGCGGCGGCGGAGG GGAGGCGGCGGCGGAGGAGGCGGCGGCGGAGGCGGCGGCGGCGGAGGAGGCGGCGGCGGCGGAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:47379256..47379389 26863196 MeRIP-seq:(Medium) rs1330569332 Functional Loss SNV dbSNP153 33..33 33 - - - 59273 RMVar_ID_59273 Human_SNP_ID_706937906 m1A Human chr22 + 49776128 49776128 49776128 TTCAGAGGCTCCAGCACCGAGGCGGCGGCATCAGTGGAGATCCACATGCTGCTCTGGCCGACTTC TTCAGAGGCTCCAGCACCGAGGCGGCGGCATCGGTGGAGATCCACATGCTGCTCTGGCCGACTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49776080..49787497 32194978 MeRIP-seq:(Medium) rs759393550 Functional Loss SNV dbSNP153 33..33 33 - - - 59274 RMVar_ID_59274 Human_SNP_ID_706941645 m1A Human chr22 + 49787603 49787602 49787603 GCTTACACTTTTCGATTTGCAGAAGAGAACAGAAGTGCGTCTGTTTACATCGCTTGCTGGCTCCG GCTTACACTTTTCGATTTGCAGAAGAGAACAG_AGTGCGTCTGTTTACATCGCTTGCTGGCTCCG GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49787596..49787697 32194978 MeRIP-seq:(Medium) rs1569097678 Functional Loss DEL dbSNP153 33..33 33 - - - 59275 RMVar_ID_59275 Human_SNP_ID_706944620 m1A Human chr22 + 49797839 49797839 49797839 TCTTCCCAGGAGAAAGGCCGCCGCGGTGCCGCAGCAGGCCGCTCAGGCAGGTGCATCCCCGAGGC TCTTCCCAGGAGAAAGGCCGCCGCGGTGCCGCCGCAGGCCGCTCAGGCAGGTGCATCCCCGAGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49787846..49798002 32194978 MeRIP-seq:(Medium) rs763870829 Functional Loss SNV dbSNP153 33..33 33 - - - 59276 RMVar_ID_59276 Human_SNP_ID_706944621 m1A Human chr22 + 49797839 49797839 49797839 TCTTCCCAGGAGAAAGGCCGCCGCGGTGCCGCAGCAGGCCGCTCAGGCAGGTGCATCCCCGAGGC TCTTCCCAGGAGAAAGGCCGCCGCGGTGCCGCGGCAGGCCGCTCAGGCAGGTGCATCCCCGAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49787846..49798002 32194978 MeRIP-seq:(Medium) rs763870829 Functional Loss SNV dbSNP153 33..33 33 - - - 59277 RMVar_ID_59277 Human_SNP_ID_706944634 m1A Human chr22 - 49797873 49797873 49797873 CCGGCGCGAGGTGGACAGCATCGGCTTGGAAGAGGCCTCGGGGATGCACCTGCCTGAGCGGCCTG CCGGCGCGAGGTGGACAGCATCGGCTTGGAAGCGGCCTCGGGGATGCACCTGCCTGAGCGGCCTG T G BRD1 Ensembl:ENSG00000100425 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:49797851..49797925 26863196 MeRIP-seq:(Medium) rs1442622656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17989932,Human_RBP_ID_18445673,Human_RBP_ID_19009480,Human_RBP_ID_23015449,Human_RBP_ID_23115761 Human_Splice_Rec_2178001,Human_Splice_Rec_2178023,Human_Splice_Rec_2178047,Human_Splice_Rec_2178071,Human_Splice_Rec_2178093 Human_miRNA_ID_2422218 RMVar_hsa_circ_52687,RMVar_hsa_circ_215182,RMVar_hsa_circ_266208,RMVar_hsa_circ_343447,RMVar_hsa_circ_123704,RMVar_hsa_circ_265202,RMVar_hsa_circ_357546,RMVar_hsa_circ_360593,RMVar_hsa_circ_298313,RMVar_hsa_circ_215183,RMVar_hsa_circ_215184,RMVar_hsa_circ_309225,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_215187,RMVar_hsa_circ_305078,RMVar_hsa_circ_215188 59278 RMVar_ID_59278 Human_SNP_ID_706953110 m1A Human chr22 - 49826859 49826859 49826859 CAGTTCACGGGAAACGCGGCTCTTGTGAGCGGACGCGGGAGTTCTGAGAATCCGTAGCAGCGGGA CAGTTCACGGGAAACGCGGCTCTTGTGAGCGGGCGCGGGAGTTCTGAGAATCCGTAGCAGCGGGA T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49826853..49826918 26863196 MeRIP-seq:(Medium) rs886956086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18498226 59279 RMVar_ID_59279 Human_SNP_ID_706953391 m1A Human chr22 - 49827565 49827565 49827565 CCGTTGGCGGAGGAGCCGCGGGCGCCATTAGCACCGCCTCGGCCGCGCCGGCCCCCGCGCCCGCC CCGTTGGCGGAGGAGCCGCGGGCGCCATTAGCCCCGCCTCGGCCGCGCCGGCCCCCGCGCCCGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:49827434..49827634 26863196 MeRIP-seq:(Medium) rs986893353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4705775 Human_Splice_Rec_2178061 59280 RMVar_ID_59280 Human_SNP_ID_706953483 m1A Human chr22 + 49827783 49827765 49827783 GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGAGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCCCGGCCGGCGGGC__________________GCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG CGCGGGCGCGGGCGCGGGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:49827702..49827800 26863410 MeRIP-seq:(Medium) rs1447965018 Functional Loss DEL dbSNP153 16..33 33 - - - 59281 RMVar_ID_59281 Human_SNP_ID_706953488 m1A Human chr22 + 49827783 49827771 49827783 GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGAGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCCCGGCCGGCGGGCGCGGGC____________GCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG CGCGGGCGCGGGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:49827702..49827800 26863410 MeRIP-seq:(Medium) rs1200394205 Functional Loss DEL dbSNP153 22..33 33 - - - 59282 RMVar_ID_59282 Human_SNP_ID_706953493 m1A Human chr22 + 49827783 49827778 49827783 GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGAGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCCCGGCCGGCGGGCGCGGGCGCGGGCG_____GCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCGGGA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:49827702..49827800 26863410 MeRIP-seq:(Medium) rs1226632157 Functional Loss DEL dbSNP153 29..33 33 - - - 59283 RMVar_ID_59283 Human_SNP_ID_706953498 m1A Human chr22 + 49827783 49827783 49827783 GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGAGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGCGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:49827702..49827800 26863410 MeRIP-seq:(Medium) rs949204844 Functional Loss SNV dbSNP153 33..33 33 - - - 59284 RMVar_ID_59284 Human_SNP_ID_706953499 m1A Human chr22 + 49827783 49827783 49827783 GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGAGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG GCCCGGCCGGCGGGCGCGGGCGCGGGCGCGGGGGCGGGCGGCGGGCGGCGGGCGCGGGACGCGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:49827702..49827800 26863410 MeRIP-seq:(Medium) rs949204844 Functional Loss SNV dbSNP153 33..33 33 - - - 59285 RMVar_ID_59285 Human_SNP_ID_706960939 m1A Human chr22 + 49853923 49853923 49853923 GGGCGCGGGGGCAGACAAAGCCGCGGTAATGAATGGAGCGTCCGCCCGCGCCGCCGTCGTCCGCA GGGCGCGGGGGCAGACAAAGCCGCGGTAATGAGTGGAGCGTCCGCCCGCGCCGCCGTCGTCCGCA A G ZBED4 Ensembl:ENSG00000100426 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49853873..49854037 26863196 MeRIP-seq:(Medium) rs1344515086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708319,Human_RBP_ID_18423796,Human_RBP_ID_27841168 Human_Splice_Rec_2178127 59286 RMVar_ID_59286 Human_SNP_ID_706960940 m1A Human chr22 + 49853927 49853927 49853927 GCGGGGGCAGACAAAGCCGCGGTAATGAATGGAGCGTCCGCCCGCGCCGCCGTCGTCCGCAGCCG GCGGGGGCAGACAAAGCCGCGGTAATGAATGGCGCGTCCGCCCGCGCCGCCGTCGTCCGCAGCCG A C ZBED4 Ensembl:ENSG00000100426 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:49853877..49854053;chr22:49853876..49883396 26863196 MeRIP-seq:(Medium) rs1295686878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708319,Human_RBP_ID_18423796,Human_RBP_ID_27841168 Human_Splice_Rec_2178127 59287 RMVar_ID_59287 Human_SNP_ID_706960955 m1A Human chr22 - 49853991 49853991 49853991 GCAGGCGGCGGGGCGGCGGCGCCCGCGCACTCACCTCGGCCCGGCCTCTGGGGCGGCTCCCGGCC GCAGGCGGCGGGGCGGCGGCGCCCGCGCACTCGCCTCGGCCCGGCCTCTGGGGCGGCTCCCGGCC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:49853891..49883336 26863410 MeRIP-seq:(Medium) rs893966783 Functional Loss SNV dbSNP153 33..33 33 - - - 59288 RMVar_ID_59288 Human_SNP_ID_706961099 m1A Human chr22 - 49854305 49854305 49854305 GCGCGCTCCCGGCGGACCCGGGCGGCGCCCCGAGCCCGAGCCCCGTCCCGTCCGCCCGGAAGCAA GCGCGCTCCCGGCGGACCCGGGCGGCGCCCCGGGCCCGAGCCCCGTCCCGTCCGCCCGGAAGCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49854301..49854398 26863196 MeRIP-seq:(Medium) rs914248685 Functional Loss SNV dbSNP153 33..33 33 - - - 59289 RMVar_ID_59289 Human_SNP_ID_706969622 m1A Human chr22 - 49883827 49883827 49883827 CAACCCGTCCCACCGAGGCCCGCTCGCTCCCCACCGCTGTCTGTCTGCTTCATGTCCTCCTGCTC CAACCCGTCCCACCGAGGCCCGCTCGCTCCCCCCCGCTGTCTGTCTGCTTCATGTCCTCCTGCTC T G lnc-ALG12-1 RNACentral:URS0000D5922D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49883777..49883937 26863196 MeRIP-seq:(Medium) rs114383207 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_195 59290 RMVar_ID_59290 Human_SNP_ID_706969773 m1A Human chr22 + 49884235 49884235 49884235 TCGTTCCCCTCTCCCTCACTCCTGCTTCCACCACAGCCTGCGGACGCGGGTGACCTCAGCACCAT TCGTTCCCCTCTCCCTCACTCCTGCTTCCACCGCAGCCTGCGGACGCGGGTGACCTCAGCACCAT A G ZBED4 Ensembl:ENSG00000100426 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs910797 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18194216 Clinvar_Rec_196 GWAS_ID_6894,GWAS_ID_6895,GWAS_ID_6896,GWAS_ID_6897,GWAS_ID_6898,GWAS_ID_6899,GWAS_ID_6900,GWAS_ID_6901,GWAS_ID_6902,GWAS_ID_6903,GWAS_ID_6904,GWAS_ID_6905,GWAS_ID_6906,GWAS_ID_6907,GWAS_ID_6908,GWAS_ID_6909,GWAS_ID_6910,GWAS_ID_6911,GWAS_ID_6912,GWAS_ID_6913,GWAS_ID_6914,GWAS_ID_6915,GWAS_ID_6916,GWAS_ID_6917,GWAS_ID_6918,GWAS_ID_6919,GWAS_ID_6920,GWAS_ID_6921,GWAS_ID_6922,GWAS_ID_6923,GWAS_ID_6924,GWAS_ID_6925,GWAS_ID_6926,GWAS_ID_6927,GWAS_ID_6928 RMVar_hsa_circ_215190 59291 RMVar_ID_59291 Human_SNP_ID_706975896 m1A Human chr22 + 49903324 49903324 49903324 TTTTATCTGTGATGGAGATGGGATGCCTGTGAATACAAAAGTTGCAGTGGTGGCACCAGGGTGGG TTTTATCTGTGATGGAGATGGGATGCCTGTGACTACAAAAGTTGCAGTGGTGGCACCAGGGTGGG A C AL671710.1 Ensembl:ENSG00000273192 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:49903276..49903428 32194978 MeRIP-seq:(Medium) rs1419175122 Functional Loss SNV dbSNP153 33..33 33 - - - 59292 RMVar_ID_59292 Human_SNP_ID_706975935 m1A Human chr22 - 49903401 49903401 49903401 GCTGCCCGAGGGCCTCTTGGGGCACCTAAGACAGCACCCCCTCTCAGGGGAGACCATGGTGGCCC GCTGCCCGAGGGCCTCTTGGGGCACCTAAGACGGCACCCCCTCTCAGGGGAGACCATGGTGGCCC T C ALG12 Ensembl:ENSG00000182858 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49903353..49903420 26863196 MeRIP-seq:(Medium) rs1164998905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_583175 RMVar_hsa_circ_89757,RMVar_hsa_circ_215193 59293 RMVar_ID_59293 Human_SNP_ID_706979169 m1A Human chr22 - 49913366 49913366 49913366 CTCTCAGCTAATAGGTAAGGGGGTCTTCAACAAAGGAGGAGGGAGTGAGGGACTGTGGTGTCATC CTCTCAGCTAATAGGTAAGGGGGTCTTCAACAGAGGAGGAGGGAGTGAGGGACTGTGGTGTCATC T C ALG12 Ensembl:ENSG00000182858 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49913363..49913497 26863196 MeRIP-seq:(Medium) rs1366132419 Functional Loss SNV dbSNP153 33..33 33 - - - 59294 RMVar_ID_59294 Human_SNP_ID_706980696 m1A Human chr22 - 49918303 49918303 49918303 TCCGCCGTCCTGCTTCCTGCCGAGGCTGGCCCAGGCAGCCGCGCTTCGAAGGACGCCGCCGGGAG TCCGCCGTCCTGCTTCCTGCCGAGGCTGGCCCGGGCAGCCGCGCTTCGAAGGACGCCGCCGGGAG T C ALG12 Ensembl:ENSG00000182858 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:49913838..49918358 32194978 MeRIP-seq:(Medium) rs981806690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708320,Human_RBP_ID_19009484,Human_RBP_ID_22272381 Human_Splice_Rec_2178129 59295 RMVar_ID_59295 Human_SNP_ID_706981176 m1A Human chr22 + 49919290 49919290 49919290 TTGGCGGCGGGAACACGGCTTGGGAGGAAAAGACGCTGTCCAAGTACGAGTCCAGGTGGGTGCCC TTGGCGGCGGGAACACGGCTTGGGAGGAAAAGGCGCTGTCCAAGTACGAGTCCAGGTGGGTGCCC A G CRELD2 Ensembl:ENSG00000184164 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49918718..49919814 26863196 MeRIP-seq:(Medium) rs1004419057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931215,Human_RBP_ID_19113752 Human_Splice_Rec_2178166,Human_Splice_Rec_2178167,Human_Splice_Rec_2178176,Human_Splice_Rec_2178177,Human_Splice_Rec_2178196,Human_Splice_Rec_2178197,Human_Splice_Rec_2178214,Human_Splice_Rec_2178215,Human_Splice_Rec_2178230,Human_Splice_Rec_2178231,Human_Splice_Rec_2178246,Human_Splice_Rec_2178247,Human_Splice_Rec_2178262,Human_Splice_Rec_2178263 59296 RMVar_ID_59296 Human_SNP_ID_706981339 m1A Human chr22 - 49919780 49919780 49919780 CCTCCTGCGCCTCTAGCATCTGATTGCATTCGAAGTCGCTGCTCTCGCACAGCCCCTCCAGGATC CCTCCTGCGCCTCTAGCATCTGATTGCATTCGGAGTCGCTGCTCTCGCACAGCCCCTCCAGGATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49919704..49919791 26863196 MeRIP-seq:(Medium) rs902493368 Functional Loss SNV dbSNP153 33..33 33 - - - 59297 RMVar_ID_59297 Human_SNP_ID_706982612 m1A Human chr22 + 49923159 49923159 49923159 TTCCCCAGCCGGCCCTGGCCACGGGCTGTGTCAGGCCATGATCGGTCCTTCCCCGCTCCCTGGCC TTCCCCAGCCGGCCCTGGCCACGGGCTGTGTCGGGCCATGATCGGTCCTTCCCCGCTCCCTGGCC A G CRELD2 Ensembl:ENSG00000184164 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49923157..49923259 26863196 MeRIP-seq:(Medium) rs1039604263 Functional Loss SNV dbSNP153 33..33 33 - - - 59298 RMVar_ID_59298 Human_SNP_ID_706984442 m1A Human chr22 + 49928087 49928087 49928087 TCACGCCGCCCCTCCTGTCGCCTCCCCGCGCCACCCCGCCGATGCCGCCAGTGGTAGGTGGCTGT TCACGCCGCCCCTCCTGTCGCCTCCCCGCGCCCCCCCGCCGATGCCGCCAGTGGTAGGTGGCTGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49928041..49928188 26863196 MeRIP-seq:(Medium) rs939110832 Functional Loss SNV dbSNP153 33..33 33 - - - 59299 RMVar_ID_59299 Human_SNP_ID_706986530 m1A Human chr22 - 49934545 49934545 49934545 GGCCACTGGGCCAGGGCCCTCCACCCTGAGTCACCCCACTGACGACCACCCTTCCCAGGTGGCAG GGCCACTGGGCCAGGGCCCTCCACCCTGAGTCGCCCCACTGACGACCACCCTTCCCAGGTGGCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:49934495..49934592 26863196 MeRIP-seq:(Medium) rs1211216793 Functional Loss SNV dbSNP153 33..33 33 - - - 59300 RMVar_ID_59300 Human_SNP_ID_706986644 m1A Human chr22 + 49934841 49934841 49934841 CTTCCCAAACCCCAAGCCGGCTGCTCTGCACCAGTGAGGGGCCGGGAGTGGCCTGGCCTGAGGAG CTTCCCAAACCCCAAGCCGGCTGCTCTGCACCGGTGAGGGGCCGGGAGTGGCCTGGCCTGAGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49934794..49934907 26863196 MeRIP-seq:(Medium) rs1344172799 Functional Loss SNV dbSNP153 33..33 33 - - - 59301 RMVar_ID_59301 Human_SNP_ID_706986836 m1A Human chr22 - 49935436 49935436 49935436 CCCATCTGCTCCCCGCCCCCGCCCGCCGGGGAAAGCCCAGCTGACGCTTCCGGCACCGCCCCCTT CCCATCTGCTCCCCGCCCCCGCCCGCCGGGGAGAGCCCAGCTGACGCTTCCGGCACCGCCCCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49935398..49935539 26863196 MeRIP-seq:(Medium) rs1395015338 Functional Loss SNV dbSNP153 33..33 33 - - - 59302 RMVar_ID_59302 Human_SNP_ID_706991990 m1A Human chr22 + 49951212 49951183 49951212 GATGGGGGCGTGGAGTCTGGGAGGCTGAGGCCAGGGGCGGAGATCTGGAGGGCTGAGGATGGGGG GATG_____________________________GGGGCGGAGATCTGGAGGGCTGAGGATGGGGG GGGGGCGTGGAGTCTGGGAGGCTGAGGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49951039..49951346 26863196 MeRIP-seq:(Medium) rs1361531377 Functional Loss DEL dbSNP153 5..33 33 - - - 59303 RMVar_ID_59303 Human_SNP_ID_706992016 m1A Human chr22 + 49951212 49951211 49951212 GATGGGGGCGTGGAGTCTGGGAGGCTGAGGCCAGGGGCGGAGATCTGGAGGGCTGAGGATGGGGG GATGGGGGCGTGGAGTCTGGGAGGCTGAGGCC_GGGGCGGAGATCTGGAGGGCTGAGGATGGGGG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49951039..49951346 26863196 MeRIP-seq:(Medium) rs1362082870 Functional Loss DEL dbSNP153 33..33 33 - - - 59304 RMVar_ID_59304 Human_SNP_ID_706993733 m1A Human chr22 + 49956538 49956538 49956538 CTCCTATCTGCAGCGGGTGAGAGGCTGCGACGACCGAGAGTGGAGGCCAGAGGGGAAAGGGCCTC CTCCTATCTGCAGCGGGTGAGAGGCTGCGACGGCCGAGAGTGGAGGCCAGAGGGGAAAGGGCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:49956489..49956670 26863196 MeRIP-seq:(Medium) rs1324133913 Functional Loss SNV dbSNP153 33..33 33 - - - 59305 RMVar_ID_59305 Human_SNP_ID_706993977 m1A Human chr22 + 49957021 49957021 49957021 GCCTCGGTAAGGGCTTGGGGGCAGGTGAGGGGACGCCCCCTCCTCAGGCATGGCCTGGGTTGGAA GCCTCGGTAAGGGCTTGGGGGCAGGTGAGGGGGCGCCCCCTCCTCAGGCATGGCCTGGGTTGGAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:49956970..49957280 26863196 MeRIP-seq:(Medium) rs947414037 Functional Loss SNV dbSNP153 33..33 33 - - - 59306 RMVar_ID_59306 Human_SNP_ID_706995325 m1A Human chr22 - 49960549 49960542 49960550 CGGGGCCGCTCCGGGACTCGTTTTCGTAGCGCAGCCGCGGAGGCGCACGGCGTGTCGCGTCGGTC CGGGGCCGCTCCGGGACTCGTTTTCGTAGCG________GAGGCGCACGGCGTGTCGCGTCGGTC CCGCGGCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49960540..49960621 26863196 MeRIP-seq:(Medium) rs1190505881 Functional Loss DEL dbSNP153 32..39 33 - - - 59307 RMVar_ID_59307 Human_SNP_ID_706995552 m1A Human chr22 - 49960957 49960957 49960957 CCCGCAGAGGTGCGCCAGGGAGCCGAACTTGGAGAGCAGCATCGCGGGCGACGGCCTCCCCGGAG CCCGCAGAGGTGCGCCAGGGAGCCGAACTTGGCGAGCAGCATCGCGGGCGACGGCCTCCCCGGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49960906..49961005 32194978 MeRIP-seq:(Medium) rs1379920544 Functional Loss SNV dbSNP153 33..33 33 - - - 59308 RMVar_ID_59308 Human_SNP_ID_706995658 m1A Human chr22 + 49961151 49961151 49961151 CTGCAGCCAAGGCGGACAAGGAGAGCTTCGAGAAGGCGTACCAGGTGGGCGCCGTGCTGGGTAGC CTGCAGCCAAGGCGGACAAGGAGAGCTTCGAGGAGGCGTACCAGGTGGGCGCCGTGCTGGGTAGC A G PIM3 Ensembl:ENSG00000198355 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:49960901..49961375 26863196 MeRIP-seq:(Medium) rs1170989804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4706149,Human_RBP_ID_19009491 Human_Splice_Rec_2178293,Human_Splice_Rec_2178298,Human_Splice_Rec_2178299 RMVar_hsa_circ_371867,RMVar_hsa_circ_215198 59309 RMVar_ID_59309 Human_SNP_ID_706995665 m1A Human chr22 + 49961161 49961161 49961161 GGCGGACAAGGAGAGCTTCGAGAAGGCGTACCAGGTGGGCGCCGTGCTGGGTAGCGGCGGCTTCG GGCGGACAAGGAGAGCTTCGAGAAGGCGTACCGGGTGGGCGCCGTGCTGGGTAGCGGCGGCTTCG A G PIM3 Ensembl:ENSG00000198355 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:49960844..49961550 26863196 MeRIP-seq:(Medium) rs1332555333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4706149,Human_RBP_ID_19009491 Human_Splice_Rec_2178293,Human_Splice_Rec_2178298,Human_Splice_Rec_2178299 RMVar_hsa_circ_371867,RMVar_hsa_circ_215198 59310 RMVar_ID_59310 Human_SNP_ID_706995668 m1A Human chr22 - 49961164 49961164 49961164 TGCCGAAGCCGCCGCTACCCAGCACGGCGCCCACCTGGTACGCCTTCTCGAAGCTCTCCTTGTCC TGCCGAAGCCGCCGCTACCCAGCACGGCGCCCGCCTGGTACGCCTTCTCGAAGCTCTCCTTGTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49960801..49961954 26863196 MeRIP-seq:(Medium) rs760885058 Functional Loss SNV dbSNP153 33..33 33 - - - 59311 RMVar_ID_59311 Human_SNP_ID_706995684 m1A Human chr22 - 49961180 49961180 49961180 CTACCCGCGTAGACCGTGCCGAAGCCGCCGCTACCCAGCACGGCGCCCACCTGGTACGCCTTCTC CTACCCGCGTAGACCGTGCCGAAGCCGCCGCTGCCCAGCACGGCGCCCACCTGGTACGCCTTCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:49961068..49961475 26863196 MeRIP-seq:(Medium) rs1421451582 Functional Loss SNV dbSNP153 33..33 33 - - - 59312 RMVar_ID_59312 Human_SNP_ID_706996076 m1A Human chr22 + 49961835 49961835 49961835 ACTTCGACGGTGAGCGCGGGCGCGGGGCAGGGAACGTTCCGGGGGCCTTGCCGGCGGGTTAACGC ACTTCGACGGTGAGCGCGGGCGCGGGGCAGGGGACGTTCCGGGGGCCTTGCCGGCGGGTTAACGC A G PIM3 Ensembl:ENSG00000198355 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49961824..49962005 26863196 MeRIP-seq:(Medium) rs776220295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833447,Human_RBP_ID_3677940,Human_RBP_ID_5387471,Human_RBP_ID_19112393,Human_RBP_ID_21985265,Human_RBP_ID_22362956,Human_RBP_ID_22674482,Human_RBP_ID_23258581,Human_RBP_ID_26789431 RMVar_hsa_circ_89523,RMVar_hsa_circ_215199 59313 RMVar_ID_59313 Human_SNP_ID_706996077 m1A Human chr22 + 49961835 49961835 49961835 ACTTCGACGGTGAGCGCGGGCGCGGGGCAGGGAACGTTCCGGGGGCCTTGCCGGCGGGTTAACGC ACTTCGACGGTGAGCGCGGGCGCGGGGCAGGGTACGTTCCGGGGGCCTTGCCGGCGGGTTAACGC A T PIM3 Ensembl:ENSG00000198355 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49961824..49962005 26863196 MeRIP-seq:(Medium) rs776220295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833447,Human_RBP_ID_3677940,Human_RBP_ID_5387471,Human_RBP_ID_19112393,Human_RBP_ID_21985265,Human_RBP_ID_22362956,Human_RBP_ID_22674482,Human_RBP_ID_23258581,Human_RBP_ID_26789431 RMVar_hsa_circ_89523,RMVar_hsa_circ_215199 59314 RMVar_ID_59314 Human_SNP_ID_706997042 m1A Human chr22 + 49963451 49963451 49963451 GCCTGCCCACCCGGAGCTCTTTCCGCCGGCGCAGGGTCCCAAGCCCACCTCCCGCCCTCAGTCCT GCCTGCCCACCCGGAGCTCTTTCCGCCGGCGCGGGGTCCCAAGCCCACCTCCCGCCCTCAGTCCT A G PIM3 Ensembl:ENSG00000198355 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr22:49963401..49963475;chr22:49963352..49963553 26863196 MeRIP-seq:(Medium) rs1210016616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_583216,Human_RBP_ID_1029981,Human_RBP_ID_4706209,Human_RBP_ID_5119970,Human_RBP_ID_17988787,Human_RBP_ID_22087234,Human_RBP_ID_22272404,Human_RBP_ID_22533847 Human_miRNA_ID_76984,Human_miRNA_ID_80152,Human_miRNA_ID_2874466,Human_miRNA_ID_2982426 RMVar_hsa_circ_111261,RMVar_hsa_circ_87503,RMVar_hsa_circ_89523,RMVar_hsa_circ_215199,RMVar_hsa_circ_215200,RMVar_hsa_circ_215201 59315 RMVar_ID_59315 Human_SNP_ID_706997232 m1A Human chr22 + 49963852 49963852 49963852 GGGTGACCCTGACACTTCCAGGCACTGTGCCCAGGGTTTGGGTTTTAAATTATTGACTTTGTACA GGGTGACCCTGACACTTCCAGGCACTGTGCCCTGGGTTTGGGTTTTAAATTATTGACTTTGTACA A T PIM3 Ensembl:ENSG00000198355 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:49963802..49964025 26863196 MeRIP-seq:(Medium) rs1322579188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029985,Human_RBP_ID_1944706,Human_RBP_ID_2727433,Human_RBP_ID_3675510,Human_RBP_ID_5149292,Human_RBP_ID_7092382,Human_RBP_ID_8865315,Human_RBP_ID_9127552,Human_RBP_ID_14528696,Human_RBP_ID_17988791,Human_RBP_ID_18330350,Human_RBP_ID_26501301 Human_miRNA_ID_76985,Human_miRNA_ID_80153 RMVar_hsa_circ_111261,RMVar_hsa_circ_87503,RMVar_hsa_circ_89523,RMVar_hsa_circ_215199,RMVar_hsa_circ_215200,RMVar_hsa_circ_215201 59316 RMVar_ID_59316 Human_SNP_ID_706999378 m1A Human chr22 + 49971349 49971349 49971349 GGATCTGGGGGCCGGGGGGCGGCGCAGAGAGCAGGGCGCGTGGGGAGCGGGAATGCGCTTTGGGG GGATCTGGGGGCCGGGGGGCGGCGCAGAGAGCCGGGCGCGTGGGGAGCGGGAATGCGCTTTGGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49971179..49971550 26863196 MeRIP-seq:(Medium) rs986096056 Functional Loss SNV dbSNP153 33..33 33 - - - 59317 RMVar_ID_59317 Human_SNP_ID_706999379 m1A Human chr22 + 49971349 49971349 49971349 GGATCTGGGGGCCGGGGGGCGGCGCAGAGAGCAGGGCGCGTGGGGAGCGGGAATGCGCTTTGGGG GGATCTGGGGGCCGGGGGGCGGCGCAGAGAGCGGGGCGCGTGGGGAGCGGGAATGCGCTTTGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49971179..49971550 26863196 MeRIP-seq:(Medium) rs986096056 Functional Loss SNV dbSNP153 33..33 33 - - - 59318 RMVar_ID_59318 Human_SNP_ID_707000124 m1A Human chr22 + 49973665 49973665 49973665 TGTGTGTGTGGTGTTTTGTGTTTGTGTGTGGTATGTATATATCATGTGTGTTGTGTGTGATGTGT TGTGTGTGTGGTGTTTTGTGTTTGTGTGTGGTGTGTATATATCATGTGTGTTGTGTGTGATGTGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:49973659..49973785 26863196 MeRIP-seq:(Medium) rs1461778597 Functional Loss SNV dbSNP153 33..33 33 - - - 59319 RMVar_ID_59319 Human_SNP_ID_707000164 m1A Human chr22 - 49973751 49973749 49973752 CCACACACAAACACCACACACCACAAAACACCACACACGCACAACACACACCATACACACACAGC CCACACACAAACACCACACACCACAAAACAC___ACACGCACAACACACACCATACACACACAGC TGTG T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:49973741..49973868 26863196 MeRIP-seq:(Medium) rs1168414613 Functional Loss DEL dbSNP153 32..34 33 - - - 59320 RMVar_ID_59320 Human_SNP_ID_707000244 m1A Human chr22 - 49975457 49975457 49975457 GCACACACCACAAAACACATGACACACACACCACACACAACACACCACACAAAACCACACACACA GCACACACCACAAAACACATGACACACACACCGCACACAACACACCACACAAAACCACACACACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:49975407..49975482 26863196 MeRIP-seq:(Medium) rs1205057424 Functional Loss SNV dbSNP153 33..33 33 - - - 59321 RMVar_ID_59321 Human_SNP_ID_707000380 m1A Human chr22 - 49975690 49975686 49975690 CAACACCACACACAGCACACACCACACAACACATGACACACACACCACACACACACCACACATGA CAACACCACACACAGCACACACCACACAACAC____CACACACACCACACACACACCACACATGA GTCAT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:49975388..49975982 26863196 MeRIP-seq:(Medium) rs1239290303 Functional Loss DEL dbSNP153 33..36 33 - - - 59322 RMVar_ID_59322 Human_SNP_ID_707000382 m1A Human chr22 - 49975690 49975688 49975690 CAACACCACACACAGCACACACCACACAACACATGACACACACACCACACACACACCACACATGA CAACACCACACACAGCACACACCACACAACAC__GACACACACACCACACACACACCACACATGA CAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:49975388..49975982 26863196 MeRIP-seq:(Medium) rs1250930550 Functional Loss DEL dbSNP153 33..34 33 - - - 59323 RMVar_ID_59323 Human_SNP_ID_707005197 m1A Human chr22 + 49992915 49992915 49992915 CTGGGATTACAGGCGGGAGCCACCGTGCCCAGACCCACCCTATTTCAGATTGCAGCTCCCCACAC CTGGGATTACAGGCGGGAGCCACCGTGCCCAGGCCCACCCTATTTCAGATTGCAGCTCCCCACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:49992909..49993132 26863196 MeRIP-seq:(Medium) rs1314576078 Functional Loss SNV dbSNP153 33..33 33 - - - 59324 RMVar_ID_59324 Human_SNP_ID_707010496 m1A Human chr22 - 50009939 50009939 50009939 CCGCCGATTCCACACCAGACTGAGGGTCACTGACTGCCGCCGATTCCACACCAGACTGAGGGTCA CCGCCGATTCCACACCAGACTGAGGGTCACTGGCTGCCGCCGATTCCACACCAGACTGAGGGTCA T C IL17REL Ensembl:ENSG00000188263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr22:50009913..50010078;chr22:50009827..50010138 26863196,32194978 MeRIP-seq:(Medium) rs1484390166 Functional Loss SNV dbSNP153 33..33 33 - - - 59325 RMVar_ID_59325 Human_SNP_ID_707010499 m1A Human chr22 + 50009964 50009964 50009964 GCGGCAGTCAGTGACCCTCAGTCTGGTGTGGAATCGGCGGCAGTCAGTGACCCTCAGTCTGGTGT GCGGCAGTCAGTGACCCTCAGTCTGGTGTGGAGTCGGCGGCAGTCAGTGACCCTCAGTCTGGTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:50009871..50009972;chr22:50009891..50010008;chr22:50009887..50010147 26863196 MeRIP-seq:(Medium) rs1209986239 Functional Loss SNV dbSNP153 33..33 33 - - - 59326 RMVar_ID_59326 Human_SNP_ID_707016795 m1A Human chr22 - 50028958 50028958 50028958 CGAGTGTGTGTGGGGGTCTTCAGGACGGTGTGATGGGGTCTTTACGAGGGTGTGTGGGGGTCTTC CGAGTGTGTGTGGGGGTCTTCAGGACGGTGTGGTGGGGTCTTTACGAGGGTGTGTGGGGGTCTTC T C TTLL8 Ensembl:ENSG00000138892 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50028952..50029098 26863196 MeRIP-seq:(Medium) rs1459976882 Functional Loss SNV dbSNP153 33..33 33 - - - 59327 RMVar_ID_59327 Human_SNP_ID_707059742 m1A Human chr22 + 50170498 50170498 50170498 CCGCTGCGGGCTCCGCGCCCGGCCAGCCCCGCACCCGCCGCGCGCCTCCGGCTACTCCCATCCCC CCGCTGCGGGCTCCGCGCCCGGCCAGCCCCGCCCCCGCCGCGCGCCTCCGGCTACTCCCATCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50170450..50170602 26863196 MeRIP-seq:(Medium) rs998515431 Functional Loss SNV dbSNP153 33..33 33 - - - 59328 RMVar_ID_59328 Human_SNP_ID_707062234 m1A Human chr22 + 50177997 50177997 50177997 CCGAGCCGCCCGTGGTCAAGCGGCCGCGCAAGAAGATGAAGTGGATCCCCACCAGCAACCCGCTT CCGAGCCGCCCGTGGTCAAGCGGCCGCGCAAGCAGATGAAGTGGATCCCCACCAGCAACCCGCTT A C PANX2 Ensembl:ENSG00000073150 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50177987..50178101 26863196 MeRIP-seq:(Medium) rs748134297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_583237 59329 RMVar_ID_59329 Human_SNP_ID_707063154 m1A Human chr22 - 50180093 50180093 50180093 GTTATTGCGTTGGGCCCCTTCACTCCTCATACATGGGCCACGCGCTGGCGTGCACTCACGCACTC GTTATTGCGTTGGGCCCCTTCACTCCTCATACGTGGGCCACGCGCTGGCGTGCACTCACGCACTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50179702..50180097 32194978 MeRIP-seq:(Medium) rs1039802732 Functional Loss SNV dbSNP153 33..33 33 - - - 59330 RMVar_ID_59330 Human_SNP_ID_707064756 m1A Human chr22 + 50185738 50185738 50185738 TGAGTGCGCGCCGATGTTCCTTAGGACCCGGGAGCGCCGGGGGGGGGGGGGGGGGCGGGGGCCCC TGAGTGCGCGCCGATGTTCCTTAGGACCCGGGGGCGCCGGGGGGGGGGGGGGGGGCGGGGGCCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50185726..50185800 26863196 MeRIP-seq:(Medium) rs1209385015 Functional Loss SNV dbSNP153 33..33 33 - - - 59331 RMVar_ID_59331 Human_SNP_ID_707065026 m1A Human chr22 - 50186153 50186153 50186153 ACCTGATCCGGGCCTGACCCCCACGACCTGCTACCCCGGCCCCAAAACCTGACCCGGGCCTGACC ACCTGATCCGGGCCTGACCCCCACGACCTGCTCCCCCGGCCCCAAAACCTGACCCGGGCCTGACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50186149..50186792 26863196 MeRIP-seq:(Medium) rs1187741178 Functional Loss SNV dbSNP153 33..33 33 - - - 59332 RMVar_ID_59332 Human_SNP_ID_707065035 m1A Human chr22 + 50186179 50186179 50186179 CCGGGGTAGCAGGTCGTGGGGGTCAGGCCCGGATCAGGTTCAGGTTTTGGGGCCGGGGGAGCAGG CCGGGGTAGCAGGTCGTGGGGGTCAGGCCCGGGTCAGGTTCAGGTTTTGGGGCCGGGGGAGCAGG A G TRABD Ensembl:ENSG00000170638 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:50186126..50186333 26863196 MeRIP-seq:(Medium) rs1187229415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5324442,Human_RBP_ID_8207570,Human_RBP_ID_9434067 RMVar_hsa_circ_104108,RMVar_hsa_circ_215213 59333 RMVar_ID_59333 Human_SNP_ID_707067581 m1A Human chr22 - 50194416 50194416 50194416 CTGCTCCCGTCCTCAGCCACCAACTGGGTCACAGTGCGCGGCAGGTTGGGCCGCTGACGCCGCCG CTGCTCCCGTCCTCAGCCACCAACTGGGTCACGGTGCGCGGCAGGTTGGGCCGCTGACGCCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50194341..50194505 26863196 MeRIP-seq:(Medium) rs1256241215 Functional Loss SNV dbSNP153 33..33 33 - - - 59334 RMVar_ID_59334 Human_SNP_ID_707068812 m1A Human chr22 + 50197936 50197936 50197936 GCACCGCACCATCGTCTCGGAGCGCGACGTCTACCTAACCTACATGCTGCGCCAGGCCGCGCGGC GCACCGCACCATCGTCTCGGAGCGCGACGTCTGCCTAACCTACATGCTGCGCCAGGCCGCGCGGC A G TRABD Ensembl:ENSG00000170638 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50197887..50198075 26863196 MeRIP-seq:(Medium) rs1268693525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029992,Human_RBP_ID_4706310,Human_RBP_ID_19008248,Human_RBP_ID_27040678 Human_Splice_Rec_2178767,Human_Splice_Rec_2178785,Human_Splice_Rec_2178819,Human_Splice_Rec_2178835 Human_miRNA_ID_1938711,Human_miRNA_ID_1949811,Human_miRNA_ID_2464450,Human_miRNA_ID_2561303,Human_miRNA_ID_2970904 RMVar_hsa_circ_104108,RMVar_hsa_circ_301565,RMVar_hsa_circ_215213,RMVar_hsa_circ_126259,RMVar_hsa_circ_215214,RMVar_hsa_circ_215215,RMVar_hsa_circ_379063 59335 RMVar_ID_59335 Human_SNP_ID_707068897 m1A Human chr22 + 50198083 50198083 50198083 CTGACCCCTTGTCCTTCCCCACAGCCGAGCCCAGGAAGTGCGTCCCCTCCGTGGTCGTGGGCGTC CTGACCCCTTGTCCTTCCCCACAGCCGAGCCCGGGAAGTGCGTCCCCTCCGTGGTCGTGGGCGTC A G TRABD Ensembl:ENSG00000170638 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50197801..50198662 32194978 MeRIP-seq:(Medium) rs1232320345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3963401,Human_RBP_ID_22550882,Human_RBP_ID_22674492,Human_RBP_ID_22744505,Human_RBP_ID_25680598 Human_Splice_Rec_2178768,Human_Splice_Rec_2178786,Human_Splice_Rec_2178820,Human_Splice_Rec_2178836 RMVar_hsa_circ_104108,RMVar_hsa_circ_301565,RMVar_hsa_circ_215213,RMVar_hsa_circ_215215,RMVar_hsa_circ_379063 59336 RMVar_ID_59336 Human_SNP_ID_707069320 m1A Human chr22 - 50198958 50198958 50198958 GTCGGCTGGAGCTCCAGGGCTGGGCCTTTCCCAGTCTCGCCTGCCCTGGAGCCCCCAGGAGCCGC GTCGGCTGGAGCTCCAGGGCTGGGCCTTTCCCGGTCTCGCCTGCCCTGGAGCCCCCAGGAGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50198909..50199006 26863196 MeRIP-seq:(Medium) rs1005313611 Functional Loss SNV dbSNP153 33..33 33 - - - 59337 RMVar_ID_59337 Human_SNP_ID_707069415 m1A Human chr22 + 50199234 50199234 50199234 CTCGCGTGCAGCCAAACATCAGCTCTGGGTCCAGGCGTGGCCTCAGCTGGGAGCCTGTGTCCTGA CTCGCGTGCAGCCAAACATCAGCTCTGGGTCCTGGCGTGGCCTCAGCTGGGAGCCTGTGTCCTGA A T TRABD Ensembl:ENSG00000170638 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50199184..50200123 32194978 MeRIP-seq:(Medium) rs905005844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_282142,Human_RBP_ID_583279,Human_RBP_ID_781609,Human_RBP_ID_1613908,Human_RBP_ID_1944715,Human_RBP_ID_5120133,Human_RBP_ID_7092438,Human_RBP_ID_9333072,Human_RBP_ID_18168806,Human_RBP_ID_18194223,Human_RBP_ID_18792087,Human_RBP_ID_26501305 Human_miRNA_ID_2510055 RMVar_hsa_circ_215216,RMVar_hsa_circ_103079 59338 RMVar_ID_59338 Human_SNP_ID_707070129 m1A Human chr22 - 50201099 50201099 50201099 GTAGAGCGGGGCGCCGGCGACGGGGAACAGCGACCGAGGGGCAAGAGTCGGGCAGCCGCGAGCGA GTAGAGCGGGGCGCCGGCGACGGGGAACAGCGGCCGAGGGGCAAGAGTCGGGCAGCCGCGAGCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50201064..50201197 26863196 MeRIP-seq:(Medium) rs5771226 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 59339 RMVar_ID_59339 Human_SNP_ID_707070137 m1A Human chr22 - 50201106 50201106 50201106 CGACAACGTAGAGCGGGGCGCCGGCGACGGGGAACAGCGACCGAGGGGCAAGAGTCGGGCAGCCG CGACAACGTAGAGCGGGGCGCCGGCGACGGGGGACAGCGACCGAGGGGCAAGAGTCGGGCAGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50201056..50201230 26863196 MeRIP-seq:(Medium) rs1415365353 Functional Loss SNV dbSNP153 33..33 33 - - - 59340 RMVar_ID_59340 Human_SNP_ID_707070144 m1A Human chr22 - 50201112 50201112 50201112 GGCGCCCGACAACGTAGAGCGGGGCGCCGGCGACGGGGAACAGCGACCGAGGGGCAAGAGTCGGG GGCGCCCGACAACGTAGAGCGGGGCGCCGGCGTCGGGGAACAGCGACCGAGGGGCAAGAGTCGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50201074..50201173 26863196 MeRIP-seq:(Medium) rs1209164880 Functional Loss SNV dbSNP153 33..33 33 - - - 59341 RMVar_ID_59341 Human_SNP_ID_707075237 m1A Human chr22 + 50215352 50215352 50215352 AAATGGCAGCTGCCTGGGCGGTGGATGGGTGGAGGCTGAGGAGTGGGGTGTGGAGGGCTCAGGAG AAATGGCAGCTGCCTGGGCGGTGGATGGGTGGGGGCTGAGGAGTGGGGTGTGGAGGGCTCAGGAG A G SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50215347..50215575 26863196 MeRIP-seq:(Medium) rs1182603550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677124,Human_RBP_ID_8208415 RMVar_hsa_circ_12707,RMVar_hsa_circ_8288,RMVar_hsa_circ_61724,RMVar_hsa_circ_58023,RMVar_hsa_circ_123246,RMVar_hsa_circ_215218 59342 RMVar_ID_59342 Human_SNP_ID_707078662 m1A Human chr22 - 50221053 50221053 50221053 GAGTCTGTGTCAGATGTGGCTCCCACTCGGCCACGGTGGAACATCCATGGACATGTGTCCAACGC GAGTCTGTGTCAGATGTGGCTCCCACTCGGCCGCGGTGGAACATCCATGGACATGTGTCCAACGC T C TUBGCP6 Ensembl:ENSG00000128159 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50221004..50221304 32194978 MeRIP-seq:(Medium) rs780958945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1944769,Human_RBP_ID_14529212 Human_miRNA_ID_2027737 RMVar_hsa_circ_75599,RMVar_hsa_circ_215220,RMVar_hsa_circ_106660,RMVar_hsa_circ_215223 59343 RMVar_ID_59343 Human_SNP_ID_707081288 m1A Human chr22 + 50227444 50227444 50227444 ACCAAGCATCTGCCACAACTCGCACCCTTCACAGCCCAGCTCCCCTGCCCCACAGTGTCTCAGCC ACCAAGCATCTGCCACAACTCGCACCCTTCACGGCCCAGCTCCCCTGCCCCACAGTGTCTCAGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:50227341..50227621;chr22:50227431..50227605 26863196 MeRIP-seq:(Medium) rs914249393 Functional Loss SNV dbSNP153 33..33 33 - - - 59344 RMVar_ID_59344 Human_SNP_ID_707081733 m1A Human chr22 - 50228643 50228633 50228643 CCGGGGGACTTGAGAGCTAGAGATGGTGGAGAAGGGGTCAGAGCAGGGGACGCTGAGAAGGGCTG CCGGGGGACTTGAGAGCTAGAGATGGTGGAGA__________GCAGGGGACGCTGAGAAGGGCTG CTCTGACCCCT C TUBGCP6 Ensembl:ENSG00000128159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50228563..50228724 26863196 MeRIP-seq:(Medium) rs904414763 Functional Loss DEL dbSNP153 33..42 33 - - - 59345 RMVar_ID_59345 Human_SNP_ID_707083683 m1A Human chr22 + 50234300 50234299 50234300 CACCCCTGTCCATGGCAGCATCACCCACACCCACCCATGGCAGCATCATCCACACCCCTGTCCAC CACCCCTGTCCATGGCAGCATCACCCACACCC_CCCATGGCAGCATCATCCACACCCCTGTCCAC CA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:50234251..50234923 26863196 MeRIP-seq:(Medium) rs1263008856 Functional Loss DEL dbSNP153 33..33 33 - - - 59346 RMVar_ID_59346 Human_SNP_ID_707083684 m1A Human chr22 + 50234300 50234300 50234300 CACCCCTGTCCATGGCAGCATCACCCACACCCACCCATGGCAGCATCATCCACACCCCTGTCCAC CACCCCTGTCCATGGCAGCATCACCCACACCCCCCCATGGCAGCATCATCCACACCCCTGTCCAC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:50234251..50234923 26863196 MeRIP-seq:(Medium) rs1451158564 Functional Loss SNV dbSNP153 33..33 33 - - - 59347 RMVar_ID_59347 Human_SNP_ID_707083685 m1A Human chr22 + 50234300 50234300 50234300 CACCCCTGTCCATGGCAGCATCACCCACACCCACCCATGGCAGCATCATCCACACCCCTGTCCAC CACCCCTGTCCATGGCAGCATCACCCACACCCGCCCATGGCAGCATCATCCACACCCCTGTCCAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:50234251..50234923 26863196 MeRIP-seq:(Medium) rs1451158564 Functional Loss SNV dbSNP153 33..33 33 - - - 59348 RMVar_ID_59348 Human_SNP_ID_707083937 m1A Human chr22 - 50234901 50234770 50234901 CCGTGGACCTGGGTGTGGATGCTGCTGTGGACAGGGGTGTGGATGATGCTGCCATGGGTGTGTGT CCGTGGACCTGGGTGTGGATGCTGCTGTGGAC_________________________________ CGTCCACAGCAGCATCCACATCCAGGTCCACAGCAGCATCATCCACACCCCCTGTCCACGACAGCATCACCCACACCCCTGTCCCTGGCAGCATCACCCACACACACCCATGGCAGCATCATCCACACCCCT C TUBGCP6 Ensembl:ENSG00000128159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50233987..50235322 26863196 MeRIP-seq:(Medium) rs1569123064 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5653675,Human_RBP_ID_23954236 59349 RMVar_ID_59349 Human_SNP_ID_707083985 m1A Human chr22 - 50234901 50234899 50234901 CCGTGGACCTGGGTGTGGATGCTGCTGTGGACAGGGGTGTGGATGATGCTGCCATGGGTGTGTGT CCGTGGACCTGGGTGTGGATGCTGCTGTGGAC__GGGTGTGGATGATGCTGCCATGGGTGTGTGT CCT C TUBGCP6 Ensembl:ENSG00000128159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50233987..50235322 26863196 MeRIP-seq:(Medium) rs111742858 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5653675,Human_RBP_ID_23954236 59350 RMVar_ID_59350 Human_SNP_ID_707083986 m1A Human chr22 - 50234901 50234901 50234901 CCGTGGACCTGGGTGTGGATGCTGCTGTGGACAGGGGTGTGGATGATGCTGCCATGGGTGTGTGT CCGTGGACCTGGGTGTGGATGCTGCTGTGGACGGGGGTGTGGATGATGCTGCCATGGGTGTGTGT T C TUBGCP6 Ensembl:ENSG00000128159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50233987..50235322 26863196 MeRIP-seq:(Medium) rs556861736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5653675,Human_RBP_ID_23954236 59351 RMVar_ID_59351 Human_SNP_ID_707087280 m1A Human chr22 + 50244392 50244392 50244392 TTGCCCTCTTCCGGTTCACACTGCGCTGGCCCAGGTGAGTCTTGGCAGCCGGCAGGAGGGCCTCA TTGCCCTCTTCCGGTTCACACTGCGCTGGCCCCGGTGAGTCTTGGCAGCCGGCAGGAGGGCCTCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50244342..50244493 32194978 MeRIP-seq:(Medium) rs746705594 Functional Loss SNV dbSNP153 33..33 33 - - - 59352 RMVar_ID_59352 Human_SNP_ID_707087281 m1A Human chr22 + 50244392 50244392 50244392 TTGCCCTCTTCCGGTTCACACTGCGCTGGCCCAGGTGAGTCTTGGCAGCCGGCAGGAGGGCCTCA TTGCCCTCTTCCGGTTCACACTGCGCTGGCCCTGGTGAGTCTTGGCAGCCGGCAGGAGGGCCTCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50244342..50244493 32194978 MeRIP-seq:(Medium) rs746705594 Functional Loss SNV dbSNP153 33..33 33 - - - 59353 RMVar_ID_59353 Human_SNP_ID_707087464 m1A Human chr22 + 50244809 50244809 50244809 CGAAACGCGCGCCCGCGCAGTACAGCGGACGAACTCGGCTTTGCACCCGTTCTTCGGGACCCACG CGAAACGCGCGCCCGCGCAGTACAGCGGACGAGCTCGGCTTTGCACCCGTTCTTCGGGACCCACG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50244802..50244970 26863196 MeRIP-seq:(Medium) rs1186124716 Functional Loss SNV dbSNP153 33..33 33 - - - 59354 RMVar_ID_59354 Human_SNP_ID_707087493 m1A Human chr22 + 50244906 50244906 50244906 AGGGTCGTGGGCAGCGGAGAGTCTGGGGGCTCAGCCGGGTGGGTCCCGGGTTCTGGCCTGCACGT AGGGTCGTGGGCAGCGGAGAGTCTGGGGGCTCGGCCGGGTGGGTCCCGGGTTCTGGCCTGCACGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50244857..50244989 26863196 MeRIP-seq:(Medium) rs1227415662 Functional Loss SNV dbSNP153 33..33 33 - - - 59355 RMVar_ID_59355 Human_SNP_ID_707087518 m1A Human chr22 + 50244967 50244967 50244967 ACGTCCACCCGTTCTCCAGGCCTCACCCGTGGAAAGTGCCCACGGCTGCCGCTCTCGCCGCCTCC ACGTCCACCCGTTCTCCAGGCCTCACCCGTGGCAAGTGCCCACGGCTGCCGCTCTCGCCGCCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50244693..50245000;chr22:50244762..50244985 26863196 MeRIP-seq:(Medium) rs917245771 Functional Loss SNV dbSNP153 33..33 33 - - - 59356 RMVar_ID_59356 Human_SNP_ID_707087670 m1A Human chr22 - 50245285 50245285 50245285 CCCGCCCCACCCATCGCGCCCCGGCCCGTCCCATCGAGGCCCATGCAACCCACGCTCGGTCCCGT CCCGCCCCACCCATCGCGCCCCGGCCCGTCCCCTCGAGGCCCATGCAACCCACGCTCGGTCCCGT T G HDAC10 Ensembl:ENSG00000100429 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:50245176..50245420 26863410 MeRIP-seq:(Medium) rs28488964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119975,Human_RBP_ID_5132975,Human_RBP_ID_17087515,Human_RBP_ID_17573107,Human_RBP_ID_18792274,Human_RBP_ID_18953176 RMVar_hsa_circ_109276,RMVar_hsa_circ_215228 59357 RMVar_ID_59357 Human_SNP_ID_707087748 m1A Human chr22 - 50245462 50245462 50245462 TGGGAGCATTTACACCGCAGAAATGACACCGCACGCCAGCGCCCCGCGGCCGCGATCCGGACCCC TGGGAGCATTTACACCGCAGAAATGACACCGCGCGCCAGCGCCCCGCGGCCGCGATCCGGACCCC T C MAPK12,HDAC10 Ensembl:ENSG00000188130,Ensembl:ENSG00000100429 Protein coding,Protein coding exon,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50245415..50245510 26863196 MeRIP-seq:(Medium) rs764144957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18168887 Human_Splice_Rec_2179136,Human_Splice_Rec_2179174,Human_Splice_Rec_2179210,Human_Splice_Rec_2179236,Human_Splice_Rec_2179266,Human_Splice_Rec_2179300,Human_Splice_Rec_2179336,Human_Splice_Rec_2179372,Human_Splice_Rec_2179390,Human_Splice_Rec_2179426,Human_Splice_Rec_2179558 RMVar_hsa_circ_109276,RMVar_hsa_circ_215228 59358 RMVar_ID_59358 Human_SNP_ID_707087931 m1A Human chr22 - 50245862 50245862 50245862 TGGAGGTGCTGCGGGGTGGGACGAGGGAAAGGACCAGTGACTGCTTCCGTCTTCGCCCCTGGTCC TGGAGGTGCTGCGGGGTGGGACGAGGGAAAGGTCCAGTGACTGCTTCCGTCTTCGCCCCTGGTCC T A MAPK12,HDAC10 Ensembl:ENSG00000188130,Ensembl:ENSG00000100429 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50245855..50246027 26863196 MeRIP-seq:(Medium) rs1482700702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931242,Human_RBP_ID_5119824,Human_RBP_ID_5387478,Human_RBP_ID_19112418,Human_RBP_ID_22362615,Human_RBP_ID_22603955,Human_RBP_ID_22674503,Human_RBP_ID_22744895,Human_RBP_ID_26789986 RMVar_hsa_circ_109276,RMVar_hsa_circ_215228 59359 RMVar_ID_59359 Human_SNP_ID_707087932 m1A Human chr22 - 50245862 50245862 50245862 TGGAGGTGCTGCGGGGTGGGACGAGGGAAAGGACCAGTGACTGCTTCCGTCTTCGCCCCTGGTCC TGGAGGTGCTGCGGGGTGGGACGAGGGAAAGGCCCAGTGACTGCTTCCGTCTTCGCCCCTGGTCC T G MAPK12,HDAC10 Ensembl:ENSG00000188130,Ensembl:ENSG00000100429 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50245855..50246027 26863196 MeRIP-seq:(Medium) rs1482700702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931242,Human_RBP_ID_5119824,Human_RBP_ID_5387478,Human_RBP_ID_19112418,Human_RBP_ID_22362615,Human_RBP_ID_22603955,Human_RBP_ID_22674503,Human_RBP_ID_22744895,Human_RBP_ID_26789986 RMVar_hsa_circ_109276,RMVar_hsa_circ_215228 59360 RMVar_ID_59360 Human_SNP_ID_707088845 m1A Human chr22 - 50247976 50247973 50247976 GCACCCTCTGTCCGCACCGCTGTTGCCCTGACAACGCCGGATATCACATTGGTTCTGCCCCCTGA GCACCCTCTGTCCGCACCGCTGTTGCCCTGAC___GCCGGATATCACATTGGTTCTGCCCCCTGA CGTT C MAPK12,HDAC10 Ensembl:ENSG00000188130,Ensembl:ENSG00000100429 Protein coding,Protein coding exon,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50247950..50248070 26863196 MeRIP-seq:(Medium) rs1158214517 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_9393160 Human_Splice_Rec_2179123,Human_Splice_Rec_2179161,Human_Splice_Rec_2179197,Human_Splice_Rec_2179225,Human_Splice_Rec_2179257,Human_Splice_Rec_2179287,Human_Splice_Rec_2179323,Human_Splice_Rec_2179359,Human_Splice_Rec_2179379,Human_Splice_Rec_2179413,Human_Splice_Rec_2179427,Human_Splice_Rec_2179437,Human_Splice_Rec_2179451,Human_Splice_Rec_2179467,Human_Splice_Rec_2179545 RMVar_hsa_circ_6554,RMVar_hsa_circ_109276,RMVar_hsa_circ_125167,RMVar_hsa_circ_215228,RMVar_hsa_circ_215229 59361 RMVar_ID_59361 Human_SNP_ID_707090319 m1A Human chr22 - 50250866 50250866 50250866 TGCGAGATCGAGCGTCCTGAGCGCCTGACCGCAGCCCTGGATCGCCTGCGGCAGCGCGGCCTGGA TGCGAGATCGAGCGTCCTGAGCGCCTGACCGCGGCCCTGGATCGCCTGCGGCAGCGCGGCCTGGA T C MAPK12,HDAC10 Ensembl:ENSG00000188130,Ensembl:ENSG00000100429 Protein coding,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50250817..50250956 26863196 MeRIP-seq:(Medium) rs1414492026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19008301,Human_RBP_ID_19112431 Human_Splice_Rec_2179104,Human_Splice_Rec_2179105,Human_Splice_Rec_2179138,Human_Splice_Rec_2179139,Human_Splice_Rec_2179176,Human_Splice_Rec_2179177,Human_Splice_Rec_2179212,Human_Splice_Rec_2179213,Human_Splice_Rec_2179238,Human_Splice_Rec_2179239,Human_Splice_Rec_2179268,Human_Splice_Rec_2179269,Human_Splice_Rec_2179302,Human_Splice_Rec_2179303,Human_Splice_Rec_2179338,Human_Splice_Rec_2179339,Human_Splice_Rec_2179392,Human_Splice_Rec_2179393,Human_Splice_Rec_2179473,Human_Splice_Rec_2179491,Human_Splice_Rec_2179497,Human_Splice_Rec_2179502,Human_Splice_Rec_2179503,Human_Splice_Rec_2179507 RMVar_hsa_circ_6554,RMVar_hsa_circ_215230,RMVar_hsa_circ_309509 59362 RMVar_ID_59362 Human_SNP_ID_707091790 m1A Human chr22 - 50254828 50254828 50254828 GAGCCGGGAGTGGTGAAAGGCAGCTGTGAGTCAGGGAACCAGGGCCCACTTAGCCCCTCCTGGCC GAGCCGGGAGTGGTGAAAGGCAGCTGTGAGTCCGGGAACCAGGGCCCACTTAGCCCCTCCTGGCC T G MAPK12 Ensembl:ENSG00000188130 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50254816..50255063 26863196 MeRIP-seq:(Medium) rs1321150947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10847,Human_RBP_ID_246291,Human_RBP_ID_583341,Human_RBP_ID_18498285,Human_RBP_ID_21986419 RMVar_hsa_circ_92910,RMVar_hsa_circ_215232 59363 RMVar_ID_59363 Human_SNP_ID_707091801 m1A Human chr22 + 50254871 50254871 50254871 TGCCTTTCACCACTCCCGGCTCCTTCTGTGCCAGCCTCTGTGCTGAGCCTGCCAGGAACACCCTT TGCCTTTCACCACTCCCGGCTCCTTCTGTGCCGGCCTCTGTGCTGAGCCTGCCAGGAACACCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50254847..50255043 26863196 MeRIP-seq:(Medium) rs1451734837 Functional Loss SNV dbSNP153 33..33 33 - - - 59364 RMVar_ID_59364 Human_SNP_ID_707092065 m1A Human chr22 - 50255265 50255265 50255265 TCCCTACTTCGAGTCCCTGCACGACACGGAAGATGAGCCCCAGGTCCAGAAGTATGATGACTCCT TCCCTACTTCGAGTCCCTGCACGACACGGAAGGTGAGCCCCAGGTCCAGAAGTATGATGACTCCT T C MAPK12 Ensembl:ENSG00000188130 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50255162..50255367 26863196 MeRIP-seq:(Medium) rs976183321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833755,Human_RBP_ID_23954275 Human_Splice_Rec_2179527,Human_Splice_Rec_2179579,Human_Splice_Rec_2179597,Human_Splice_Rec_2179619,Human_Splice_Rec_2179639,Human_Splice_Rec_2179659 RMVar_hsa_circ_92910,RMVar_hsa_circ_215233,RMVar_hsa_circ_321799,RMVar_hsa_circ_215232,RMVar_hsa_circ_372252,RMVar_hsa_circ_215234 59365 RMVar_ID_59365 Human_SNP_ID_707094664 m1A Human chr22 + 50261477 50261477 50261477 TCCCAGGCCGTCTTGGTCACCTCCTGGCGGTAAAAGCCACTGCGGGCGGGCGGCGGAGAGCTCAT TCCCAGGCCGTCTTGGTCACCTCCTGGCGGTAGAAGCCACTGCGGGCGGGCGGCGGAGAGCTCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50261375..50261771 26863196 MeRIP-seq:(Medium) rs1293193597 Functional Loss SNV dbSNP153 33..33 33 - - - 59366 RMVar_ID_59366 Human_SNP_ID_707094716 m1A Human chr22 - 50261592 50261592 50261592 GGCGAGCGGACGAGCGGCGCGGAGCCGGCCCGAGGCGCGCGCCGAGGGAGCCCCGTCCCCGGTCG GGCGAGCGGACGAGCGGCGCGGAGCCGGCCCGGGGCGCGCGCCGAGGGAGCCCCGTCCCCGGTCG T C MAPK12 Ensembl:ENSG00000188130 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:50261498..50261665 26863410 MeRIP-seq:(Medium) rs1188390882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_265791,Human_RBP_ID_929637,Human_RBP_ID_5119825,Human_RBP_ID_5389673,Human_RBP_ID_17671138,Human_RBP_ID_19112442,Human_RBP_ID_21986424,Human_RBP_ID_26345601,Human_RBP_ID_27841322 Human_miRNA_ID_2018158 RMVar_hsa_circ_215235,RMVar_hsa_circ_109519,RMVar_hsa_circ_215241 59367 RMVar_ID_59367 Human_SNP_ID_707094733 m1A Human chr22 - 50261620 50261620 50261620 GAGCGCCCCAGCGGCCGGCGGGCGGGCGGGCGAGCGGACGAGCGGCGCGGAGCCGGCCCGAGGCG GAGCGCCCCAGCGGCCGGCGGGCGGGCGGGCGGGCGGACGAGCGGCGCGGAGCCGGCCCGAGGCG T C MAPK12 Ensembl:ENSG00000188130 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr22:50261533..50261725;chr22:50261525..50261703 26863196,26863410 MeRIP-seq:(Medium) rs187578301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_265791,Human_RBP_ID_833764,Human_RBP_ID_929637,Human_RBP_ID_3963443,Human_RBP_ID_5119825,Human_RBP_ID_5389673,Human_RBP_ID_9333087,Human_RBP_ID_17671138,Human_RBP_ID_18423673,Human_RBP_ID_19008316,Human_RBP_ID_19112443,Human_RBP_ID_21986424,Human_RBP_ID_23258585,Human_RBP_ID_26345601,Human_RBP_ID_27841322 RMVar_hsa_circ_215235,RMVar_hsa_circ_109519,RMVar_hsa_circ_215241 59368 RMVar_ID_59368 Human_SNP_ID_707094761 m1A Human chr22 - 50261687 50261687 50261687 GCAGCCTGGGTCGGGGTCGGGCCGGGGTCGGCACCTGGGACATCCCTGAGGGAAGGGCCGGGAGC GCAGCCTGGGTCGGGGTCGGGCCGGGGTCGGCGCCTGGGACATCCCTGAGGGAAGGGCCGGGAGC T C MAPK12 Ensembl:ENSG00000188130 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50261377..50261773 26863196 MeRIP-seq:(Medium) rs968717872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246770,Human_RBP_ID_929637,Human_RBP_ID_9333571,Human_RBP_ID_17671138,Human_RBP_ID_18423673,Human_RBP_ID_19112443,Human_RBP_ID_21985663,Human_RBP_ID_26345601,Human_RBP_ID_27821432 RMVar_hsa_circ_215235 59369 RMVar_ID_59369 Human_SNP_ID_707094889 m1A Human chr22 - 50261984 50261984 50261984 GGCGGGGGGGGGGGGGGGGGGCTCCTGCTGAGACCCCCCCAGGGCGGGGAAGTTCAGCCAAAGGG GGCGGGGGGGGGGGGGGGGGGCTCCTGCTGAGGCCCCCCCAGGGCGGGGAAGTTCAGCCAAAGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50261976..50262025 26863196 MeRIP-seq:(Medium) rs1007756850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215235 59370 RMVar_ID_59370 Human_SNP_ID_707094890 m1A Human chr22 - 50261984 50261984 50261984 GGCGGGGGGGGGGGGGGGGGGCTCCTGCTGAGACCCCCCCAGGGCGGGGAAGTTCAGCCAAAGGG GGCGGGGGGGGGGGGGGGGGGCTCCTGCTGAGCCCCCCCCAGGGCGGGGAAGTTCAGCCAAAGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50261976..50262025 26863196 MeRIP-seq:(Medium) rs1007756850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215235 59371 RMVar_ID_59371 Human_SNP_ID_707095838 m1A Human chr22 + 50264964 50264964 50264964 GCTGCTGGGCAGCACCTCACTGCTCAATCTCCAGGCTGCCAGGTGGCTTCGGTGGCTCTGGGGGC GCTGCTGGGCAGCACCTCACTGCTCAATCTCCCGGCTGCCAGGTGGCTTCGGTGGCTCTGGGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50264913..50265032 26863196 MeRIP-seq:(Medium) rs200627432 Functional Loss SNV dbSNP153 33..33 33 - - - 59372 RMVar_ID_59372 Human_SNP_ID_707095839 m1A Human chr22 + 50264964 50264964 50264964 GCTGCTGGGCAGCACCTCACTGCTCAATCTCCAGGCTGCCAGGTGGCTTCGGTGGCTCTGGGGGC GCTGCTGGGCAGCACCTCACTGCTCAATCTCCTGGCTGCCAGGTGGCTTCGGTGGCTCTGGGGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50264913..50265032 26863196 MeRIP-seq:(Medium) rs200627432 Functional Loss SNV dbSNP153 33..33 33 - - - 59373 RMVar_ID_59373 Human_SNP_ID_707096173 m1A Human chr22 - 50265867 50265867 50265867 GGCAGTGGGGGTGGGCTGGGTGGAGGGAGTGTACTTGGACCCAGCTCCTGCAGGCATTAGGGGCC GGCAGTGGGGGTGGGCTGGGTGGAGGGAGTGTTCTTGGACCCAGCTCCTGCAGGCATTAGGGGCC T A MAPK11 Ensembl:ENSG00000185386 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50265864..50266109 26863196 MeRIP-seq:(Medium) rs1158077854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9433576 RMVar_hsa_circ_215235,RMVar_hsa_circ_103977,RMVar_hsa_circ_105769,RMVar_hsa_circ_215245,RMVar_hsa_circ_215244 59374 RMVar_ID_59374 Human_SNP_ID_707096650 m1A Human chr22 + 50267073 50267073 50267073 TCCAGGATCTGGGGCGACCACGTGGTGTTCTCAAGCTCCGCACGGGCTCCGCCGCCGCCCTGCCC TCCAGGATCTGGGGCGACCACGTGGTGTTCTCCAGCTCCGCACGGGCTCCGCCGCCGCCCTGCCC A C NONHSAG034238.2 RNACentral:URS00008C1ADF lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:50267071..50267270 26863196 MeRIP-seq:(Medium) rs1435378252 Functional Loss SNV dbSNP153 33..33 33 - - - 59375 RMVar_ID_59375 Human_SNP_ID_707099534 m1A Human chr22 - 50275186 50275184 50275186 TCCCCAAGGGTGCCGGCACTCTGGGTGGACTCACGGCTGCTGGGCCCCACGTCAAAGGTCAAGTG TCCCCAAGGGTGCCGGCACTCTGGGTGGACTC__GGCTGCTGGGCCCCACGTCAAAGGTCAAGTG CGT C PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50275001..50276855 32194978 MeRIP-seq:(Medium) rs896865672 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_583360,Human_RBP_ID_5119826,Human_RBP_ID_8865341,Human_RBP_ID_17287120,Human_RBP_ID_17988888,Human_RBP_ID_27495854 RMVar_hsa_circ_84415,RMVar_hsa_circ_117661,RMVar_hsa_circ_121954,RMVar_hsa_circ_126413,RMVar_hsa_circ_123581,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_93675,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_215258,RMVar_hsa_circ_215260,RMVar_hsa_circ_79920,RMVar_hsa_circ_215259,RMVar_hsa_circ_215257,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_377561,RMVar_hsa_circ_215249,RMVar_hsa_circ_215261 59376 RMVar_ID_59376 Human_SNP_ID_707100876 m1A Human chr22 + 50278154 50278154 50278154 CTGAGAGCAGCCGCGTCAGGTAGATCTCGGTGATGGCCTTCGTCCGCTCCTTCTCTTTCACGCTG CTGAGAGCAGCCGCGTCAGGTAGATCTCGGTGGTGGCCTTCGTCCGCTCCTTCTCTTTCACGCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50278151..50278175 26863196 MeRIP-seq:(Medium) rs1198992174 Functional Loss SNV dbSNP153 33..33 33 - - - 59377 RMVar_ID_59377 Human_SNP_ID_707100895 m1A Human chr22 - 50278177 50278177 50278177 GACGAGGGCAAGTCCAAGAGAGGCAGCGTGAAAGAGAAGGAGCGGACGAAGGCCATCACCGAGAT GACGAGGGCAAGTCCAAGAGAGGCAGCGTGAAGGAGAAGGAGCGGACGAAGGCCATCACCGAGAT T C PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50278126..50278276 26863196 MeRIP-seq:(Medium) rs199645325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65641 Human_Splice_Rec_2179772,Human_Splice_Rec_2179773,Human_Splice_Rec_2179808,Human_Splice_Rec_2179809,Human_Splice_Rec_2179848,Human_Splice_Rec_2179849,Human_Splice_Rec_2179920,Human_Splice_Rec_2179921,Human_Splice_Rec_2179992,Human_Splice_Rec_2179993,Human_Splice_Rec_2180024,Human_Splice_Rec_2180025,Human_Splice_Rec_2180050,Human_Splice_Rec_2180051,Human_Splice_Rec_2180060,Human_Splice_Rec_2180061 Human_miRNA_ID_3119339 RMVar_hsa_circ_84415,RMVar_hsa_circ_117661,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215257,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267 59378 RMVar_ID_59378 Human_SNP_ID_707100914 m1A Human chr22 - 50278221 50278221 50278221 AGGAGAACCGGGTGTGGCACCTGGTGCGGCCGACCGACGAGGTGGACGAGGGCAAGTCCAAGAGA AGGAGAACCGGGTGTGGCACCTGGTGCGGCCGCCCGACGAGGTGGACGAGGGCAAGTCCAAGAGA T G PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50278201..50278225 26863196 MeRIP-seq:(Medium) rs879151685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22454780 Human_Splice_Rec_2179772,Human_Splice_Rec_2179808,Human_Splice_Rec_2179848,Human_Splice_Rec_2179920,Human_Splice_Rec_2179992,Human_Splice_Rec_2180024,Human_Splice_Rec_2180050,Human_Splice_Rec_2180060 RMVar_hsa_circ_84415,RMVar_hsa_circ_117661,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215257,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267 59379 RMVar_ID_59379 Human_SNP_ID_707100983 m1A Human chr22 - 50278403 50278403 50278403 CGTGAGTCCCTCCCTGTTGCCCGTTTCCTTCCAGCCCCTGGTGGTCAGCGTGGACCATGTCTGCC CGTGAGTCCCTCCCTGTTGCCCGTTTCCTTCCGGCCCCTGGTGGTCAGCGTGGACCATGTCTGCC T C PLXNB2 Ensembl:ENSG00000196576 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50278397..50278500 26863196 MeRIP-seq:(Medium) rs1046534592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5388602,Human_RBP_ID_19113818,Human_RBP_ID_23258508,Human_RBP_ID_24494713 RMVar_hsa_circ_84415,RMVar_hsa_circ_117661,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215257,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267 59380 RMVar_ID_59380 Human_SNP_ID_707101225 m1A Human chr22 - 50279005 50279005 50279005 GGGCTTCATCCCGGATGTCTCGGCAGACGGTGAGCGTGATCGTGCAGGACGAGGGAGTGGACGCC GGGCTTCATCCCGGATGTCTCGGCAGACGGTGTGCGTGATCGTGCAGGACGAGGGAGTGGACGCC T A PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50278995..50279168 26863196 MeRIP-seq:(Medium) rs768751941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3963451,Human_RBP_ID_22675507,Human_RBP_ID_26346173 Human_Splice_Rec_2179802,Human_Splice_Rec_2179842,Human_Splice_Rec_2179914,Human_Splice_Rec_2179986,Human_Splice_Rec_2180018,Human_Splice_Rec_2180044 RMVar_hsa_circ_84415,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_49361,RMVar_hsa_circ_97641,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267,RMVar_hsa_circ_83697,RMVar_hsa_circ_215268,RMVar_hsa_circ_215269 59381 RMVar_ID_59381 Human_SNP_ID_707101460 m1A Human chr22 - 50279691 50279691 50279691 GGAAAAGGGCCCGGTGGATGCGGTACAGAAGAAGGCCAAGTACACTCTCAACGACACGGGGCTGC GGAAAAGGGCCCGGTGGATGCGGTACAGAAGACGGCCAAGTACACTCTCAACGACACGGGGCTGC T G PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:50279612..50279751;chr22:50279588..50279710 26863196 MeRIP-seq:(Medium) rs764463882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23015043,Human_RBP_ID_26345604 Human_Splice_Rec_2179800,Human_Splice_Rec_2179801,Human_Splice_Rec_2179840,Human_Splice_Rec_2179841,Human_Splice_Rec_2179912,Human_Splice_Rec_2179913,Human_Splice_Rec_2179984,Human_Splice_Rec_2179985,Human_Splice_Rec_2180016,Human_Splice_Rec_2180017,Human_Splice_Rec_2180042,Human_Splice_Rec_2180043 RMVar_hsa_circ_84415,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_49361,RMVar_hsa_circ_97641,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267,RMVar_hsa_circ_83697,RMVar_hsa_circ_215268,RMVar_hsa_circ_116987,RMVar_hsa_circ_215269,RMVar_hsa_circ_215270 59382 RMVar_ID_59382 Human_SNP_ID_707103843 m1A Human chr22 + 50284902 50284902 50284902 TCCTCTGTGGGTTTCCCACGGCCACCTCCACCACTCATCCACACCTGAGAACATCGCCCGGCCCA TCCTCTGTGGGTTTCCCACGGCCACCTCCACCCCTCATCCACACCTGAGAACATCGCCCGGCCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50284676..50285203 26863196 MeRIP-seq:(Medium) rs868362415 Functional Loss SNV dbSNP153 33..33 33 - - - 59383 RMVar_ID_59383 Human_SNP_ID_707105802 m1A Human chr22 - 50289776 50289776 50289776 CCTGGAGATGGACCTGCAGTGCCGGGACCCCGACATCCACGCCGCTGCCTTTGGCACCTGCCTGG CCTGGAGATGGACCTGCAGTGCCGGGACCCCGCCATCCACGCCGCTGCCTTTGGCACCTGCCTGG T G PLXNB2 Ensembl:ENSG00000196576 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50289726..50290143 26863196 MeRIP-seq:(Medium) rs1020040133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_583381 RMVar_hsa_circ_126413,RMVar_hsa_circ_215249,RMVar_hsa_circ_111551,RMVar_hsa_circ_215265,RMVar_hsa_circ_105885,RMVar_hsa_circ_215275,RMVar_hsa_circ_346969,RMVar_hsa_circ_349327 59384 RMVar_ID_59384 Human_SNP_ID_707105945 m1A Human chr22 + 50290099 50290099 50290099 CCTTTGCCCACAAACAGCACGCGGTCACCACCAGGACCCGTGGAGCTCACCAGCCCCACTGTGGC CCTTTGCCCACAAACAGCACGCGGTCACCACCGGGACCCGTGGAGCTCACCAGCCCCACTGTGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50290002..50290300 32194978 MeRIP-seq:(Medium) rs760284158 Functional Loss SNV dbSNP153 33..33 33 - - - 59385 RMVar_ID_59385 Human_SNP_ID_707106108 m1A Human chr22 + 50290547 50290547 50290547 TGCGGGGCCTCAGGCTGGCACCTGCGCCCAGCAGGCCCAGCAGGGTCAGGGCCCAGAGCTGCAGT TGCGGGGCCTCAGGCTGGCACCTGCGCCCAGCGGGCCCAGCAGGGTCAGGGCCCAGAGCTGCAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr22:50290501..50290575 26863196,32194978 MeRIP-seq:(Medium) rs1370982481 Functional Loss SNV dbSNP153 33..33 33 - - - 59386 RMVar_ID_59386 Human_SNP_ID_707107010 m1A Human chr22 - 50293474 50293473 50293474 GGCTGGGAGGGGAGGGCAGCAGGCCTGGGCGCAGGGCCGAGGGGCCTGGACGTTGCCTGCCCCCG GGCTGGGAGGGGAGGGCAGCAGGCCTGGGCGC_GGGCCGAGGGGCCTGGACGTTGCCTGCCCCCG CT C PLXNB2 Ensembl:ENSG00000196576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50293469..50293537 26863196 MeRIP-seq:(Medium) rs201443345 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3677141,Human_RBP_ID_5204118,Human_RBP_ID_5389706,Human_RBP_ID_8207620,Human_RBP_ID_8729548,Human_RBP_ID_18952750,Human_RBP_ID_22725340 RMVar_hsa_circ_111551,RMVar_hsa_circ_215265,RMVar_hsa_circ_349327 59387 RMVar_ID_59387 Human_SNP_ID_707107011 m1A Human chr22 - 50293474 50293474 50293474 GGCTGGGAGGGGAGGGCAGCAGGCCTGGGCGCAGGGCCGAGGGGCCTGGACGTTGCCTGCCCCCG GGCTGGGAGGGGAGGGCAGCAGGCCTGGGCGCGGGGCCGAGGGGCCTGGACGTTGCCTGCCCCCG T C PLXNB2 Ensembl:ENSG00000196576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50293469..50293537 26863196 MeRIP-seq:(Medium) rs28455041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677141,Human_RBP_ID_5204118,Human_RBP_ID_5389706,Human_RBP_ID_8207620,Human_RBP_ID_8729548,Human_RBP_ID_18952750,Human_RBP_ID_22725340 RMVar_hsa_circ_111551,RMVar_hsa_circ_215265,RMVar_hsa_circ_349327 59388 RMVar_ID_59388 Human_SNP_ID_707107405 m1A Human chr22 + 50294676 50294676 50294676 CAGTTCTAGATACCTCCGGCCTCCCTGTCCACATAGCCCCAGCCACCCACTGCCTTTCCCAGGTG CAGTTCTAGATACCTCCGGCCTCCCTGTCCACGTAGCCCCAGCCACCCACTGCCTTTCCCAGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50294673..50294809 26863196 MeRIP-seq:(Medium) rs1239890966 Functional Loss SNV dbSNP153 33..33 33 - - - 59389 RMVar_ID_59389 Human_SNP_ID_707109891 m1A Human chr22 + 50302955 50302955 50302955 GAAAACACACCTGACAGGGCTGGGATCCACAGAGTCCTCACCTCCTGCTGGTCCTCAAACCCCAC GAAAACACACCTGACAGGGCTGGGATCCACAGCGTCCTCACCTCCTGCTGGTCCTCAAACCCCAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50302952..50303038 26863196 MeRIP-seq:(Medium) rs1332661523 Functional Loss SNV dbSNP153 33..33 33 - - - 59390 RMVar_ID_59390 Human_SNP_ID_707110940 m1A Human chr22 - 50306666 50306666 50306666 GGGTGAGGGTGAGGGTGGGCCCCAAACCCGGCAGATCCCGGCGGCCTGGAGGGCTCCCTGTGCCC GGGTGAGGGTGAGGGTGGGCCCCAAACCCGGCGGATCCCGGCGGCCTGGAGGGCTCCCTGTGCCC T C PLXNB2 Ensembl:ENSG00000196576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50306664..50306732 26863196 MeRIP-seq:(Medium) rs1201537101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677208,Human_RBP_ID_5325087,Human_RBP_ID_5388629,Human_RBP_ID_8207676,Human_RBP_ID_22725373,Human_RBP_ID_24553827,Human_RBP_ID_26790015 RMVar_hsa_circ_111551,RMVar_hsa_circ_215265 59391 RMVar_ID_59391 Human_SNP_ID_707111297 m1A Human chr22 - 50307602 50307602 50307602 CGTCTCCATGGCAGCAGCGCGGGCCAGAGCGCAGCGCCGAGCGCGGCCCGGGCGCCATCGAGCCT CGTCTCCATGGCAGCAGCGCGGGCCAGAGCGCGGCGCCGAGCGCGGCCCGGGCGCCATCGAGCCT T C PLXNB2 Ensembl:ENSG00000196576 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:50307495..50307650;chr22:50307460..50307625 26863196 MeRIP-seq:(Medium) rs1396855670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707072 Human_Splice_Rec_2179861,Human_Splice_Rec_2179933,Human_Splice_Rec_2180101 59392 RMVar_ID_59392 Human_SNP_ID_707111298 m1A Human chr22 - 50307602 50307602 50307602 CGTCTCCATGGCAGCAGCGCGGGCCAGAGCGCAGCGCCGAGCGCGGCCCGGGCGCCATCGAGCCT CGTCTCCATGGCAGCAGCGCGGGCCAGAGCGCCGCGCCGAGCGCGGCCCGGGCGCCATCGAGCCT T G PLXNB2 Ensembl:ENSG00000196576 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:50307495..50307650;chr22:50307460..50307625 26863196 MeRIP-seq:(Medium) rs1396855670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707072 Human_Splice_Rec_2179861,Human_Splice_Rec_2179933,Human_Splice_Rec_2180101 59393 RMVar_ID_59393 Human_SNP_ID_707120870 m1A Human chr22 + 50337109 50337109 50337109 AAAAACCAAGCAGGGAAGGTGGTGATGAAGAGAGTGTGTGTGTGTGTGTGTGTGTGGTGTGTCTG AAAAACCAAGCAGGGAAGGTGGTGATGAAGAGTGTGTGTGTGTGTGTGTGTGTGTGGTGTGTCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50337106..50338531 26863196 MeRIP-seq:(Medium) rs1210370959 Functional Loss SNV dbSNP153 33..33 33 - - - 59394 RMVar_ID_59394 Human_SNP_ID_707120904 m1A Human chr22 - 50337166 50337164 50337167 CAGCACACACGCACACACCCCACACACACCACACATCGCACACACACACTGTACACACAGACACA CAGCACACACGCACACACCCCACACACACCA___ATCGCACACACACACTGTACACACAGACACA TGTG T lnc-DENND6B-1,lnc-DENND6B-1:2 RNACentral:URS00008B5232,RNACentral:URS00008BDF53 lincRNA,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50337115..50337239 26863196 MeRIP-seq:(Medium) rs982838232 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2727555 59395 RMVar_ID_59395 Human_SNP_ID_707121308 m1A Human chr22 - 50337835 50337835 50337835 ACACAGACACACCAACACACCACACACACCCCACACACACACTGTACCCAGATAGCACACATGCC ACACAGACACACCAACACACCACACACACCCCCCACACACACTGTACCCAGATAGCACACATGCC T G lnc-DENND6B-1,lnc-DENND6B-1:2,lnc-DENND6B-1:3 RNACentral:URS00008B5232,RNACentral:URS00008B787C,RNACentral:URS00008BDF53 lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50337826..50337974 26863196 MeRIP-seq:(Medium) rs898250279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2727569 59396 RMVar_ID_59396 Human_SNP_ID_707121560 m1A Human chr22 - 50338230 50338209 50338230 ACCACACATAGACACAAACACACCACACACACACACCAACACACCACACACACCCCCGACACACA ACCACACATAGACACAAACACACCACACACAC_____________________CCCCGACACACA GGTGTGTGTGGTGTGTTGGTGT G lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50337968..50338495 26863196 MeRIP-seq:(Medium) rs1400733187 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_2727575 59397 RMVar_ID_59397 Human_SNP_ID_707121571 m1A Human chr22 - 50338230 50338226 50338230 ACCACACATAGACACAAACACACCACACACACACACCAACACACCACACACACCCCCGACACACA ACCACACATAGACACAAACACACCACACACAC____CAACACACCACACACACCCCCGACACACA GGTGT G lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50337968..50338495 26863196 MeRIP-seq:(Medium) rs371044844 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_2727575 59398 RMVar_ID_59398 Human_SNP_ID_707121572 m1A Human chr22 - 50338230 50338226 50338230 ACCACACATAGACACAAACACACCACACACACACACCAACACACCACACACACCCCCGACACACA ACCACACATAGACACAAACACACCACACACAC__ACCAACACACCACACACACCCCCGACACACA GGTGT GGT lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50337968..50338495 26863196 MeRIP-seq:(Medium) rs371044844 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2727575 59399 RMVar_ID_59399 Human_SNP_ID_707121849 m1A Human chr22 + 50338610 50338603 50338610 GGTGTGTGTTTGTGGTGTGTGGTGTGTGTGGTATGTAGTATGTGTGGTATATGGTGTGTGGTGTC GGTGTGTGTTTGTGGTGTGTGGTGTG_______TGTAGTATGTGTGGTATATGGTGTGTGGTGTC GTGTGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50338601..50338889 26863196 MeRIP-seq:(Medium) rs1270668522 Functional Loss DEL dbSNP153 27..33 33 - - - 59400 RMVar_ID_59400 Human_SNP_ID_707121863 m1A Human chr22 - 50338634 50338634 50338634 ATACCACACACACTACATACCACAGACACCACACACCATATACCACACATACTACATACCACACA ATACCACACACACTACATACCACAGACACCACGCACCATATACCACACATACTACATACCACACA T C lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338550..50338669 26863196 MeRIP-seq:(Medium) rs923902967 Functional Loss SNV dbSNP153 33..33 33 - - - 59401 RMVar_ID_59401 Human_SNP_ID_707121864 m1A Human chr22 - 50338634 50338634 50338634 ATACCACACACACTACATACCACAGACACCACACACCATATACCACACATACTACATACCACACA ATACCACACACACTACATACCACAGACACCACCCACCATATACCACACATACTACATACCACACA T G lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338550..50338669 26863196 MeRIP-seq:(Medium) rs923902967 Functional Loss SNV dbSNP153 33..33 33 - - - 59402 RMVar_ID_59402 Human_SNP_ID_707121946 m1A Human chr22 - 50338779 50338749 50338779 ACCAGACACCGTACATACACACCACACACACCACATACCACACACACTACCTACCACACATACCA ACCAGACACCGTACATACACACCACACACACC______________________________CCA GTATGTGTGGTAGGTAGTGTGTGTGGTATGT G lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338731..50338896 26863196 MeRIP-seq:(Medium) rs1569218456 Functional Loss DEL dbSNP153 33..62 33 - - - 59403 RMVar_ID_59403 Human_SNP_ID_707121961 m1A Human chr22 - 50338779 50338775 50338780 ACCAGACACCGTACATACACACCACACACACCACATACCACACACACTACCTACCACACATACCA ACCAGACACCGTACATACACACCACACACAC_____ACCACACACACTACCTACCACACATACCA TATGTG T lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338731..50338896 26863196 MeRIP-seq:(Medium) rs1387285231 Functional Loss DEL dbSNP153 32..36 33 - - - 59404 RMVar_ID_59404 Human_SNP_ID_707122087 m1A Human chr22 + 50338964 50338955 50338964 GTGTGTGGGTGTGTAGGGTGTGGTGGGTGTGTAGGGTGTGTGGTGTGTGTGTGGTATGTAGTATG GTGTGTGGGTGTGTAGGGTGTGGT_________GGGTGTGTGGTGTGTGTGTGGTATGTAGTATG TGGGTGTGTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50338962..50339760 26863196 MeRIP-seq:(Medium) rs1321387383 Functional Loss DEL dbSNP153 25..33 33 - - - 59405 RMVar_ID_59405 Human_SNP_ID_707122093 m1A Human chr22 + 50338964 50338964 50338964 GTGTGTGGGTGTGTAGGGTGTGGTGGGTGTGTAGGGTGTGTGGTGTGTGTGTGGTATGTAGTATG GTGTGTGGGTGTGTAGGGTGTGGTGGGTGTGTGGGGTGTGTGGTGTGTGTGTGGTATGTAGTATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50338962..50339760 26863196 MeRIP-seq:(Medium) rs566984019 Functional Loss SNV dbSNP153 33..33 33 - - - 59406 RMVar_ID_59406 Human_SNP_ID_707122094 m1A Human chr22 + 50338964 50338964 50338964 GTGTGTGGGTGTGTAGGGTGTGGTGGGTGTGTAGGGTGTGTGGTGTGTGTGTGGTATGTAGTATG GTGTGTGGGTGTGTAGGGTGTGGTGGGTGTGTTGGGTGTGTGGTGTGTGTGTGGTATGTAGTATG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50338962..50339760 26863196 MeRIP-seq:(Medium) rs566984019 Functional Loss SNV dbSNP153 33..33 33 - - - 59407 RMVar_ID_59407 Human_SNP_ID_707122272 m1A Human chr22 + 50339202 50339202 50339202 GTGGTGTGCGTGTGGTATGTAGTGTGTGTTGTATGTGGTGTGTGTGTAGGGTGTGTGGTGTGTTT GTGGTGTGCGTGTGGTATGTAGTGTGTGTTGTGTGTGGTGTGTGTGTAGGGTGTGTGGTGTGTTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50339195..50339376 26863196 MeRIP-seq:(Medium) rs1465802132 Functional Loss SNV dbSNP153 33..33 33 - - - 59408 RMVar_ID_59408 Human_SNP_ID_707122509 m1A Human chr22 - 50339555 50339547 50339556 ACACCACACACACACTACATACCACACACACCACACACACACCACACACACACCACACACCACAT ACACCACACACACACTACATACCACACACAC_________ACCACACACACACCACACACCACAT TGTGTGTGTG T lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338966..50339751 26863196 MeRIP-seq:(Medium) rs1399383806 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_2727598 59409 RMVar_ID_59409 Human_SNP_ID_707122512 m1A Human chr22 - 50339555 50339555 50339555 ACACCACACACACACTACATACCACACACACCACACACACACCACACACACACCACACACCACAT ACACCACACACACACTACATACCACACACACCCCACACACACCACACACACACCACACACCACAT T G lnc-DENND6B-1 RNACentral:URS00008B787C lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50338966..50339751 26863196 MeRIP-seq:(Medium) rs1342216365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2727598 59410 RMVar_ID_59410 Human_SNP_ID_707122787 m1A Human chr22 - 50339893 50339891 50339893 CACACACACACCACATACCACACACACCACACACCCCACACACACACCACACCACACACACACTA CACACACACACCACATACCACACACACCACAC__CCCACACACACACCACACCACACACACACTA GGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50339890..50340563 26863196 MeRIP-seq:(Medium) rs1345200917 Functional Loss DEL dbSNP153 33..34 33 - - - 59411 RMVar_ID_59411 Human_SNP_ID_707122789 m1A Human chr22 - 50339893 50339893 50339893 CACACACACACCACATACCACACACACCACACACCCCACACACACACCACACCACACACACACTA CACACACACACCACATACCACACACACCACACCCCCCACACACACACCACACCACACACACACTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50339890..50340563 26863196 MeRIP-seq:(Medium) rs1333127383 Functional Loss SNV dbSNP153 33..33 33 - - - 59412 RMVar_ID_59412 Human_SNP_ID_707124077 m1A Human chr22 + 50343379 50343379 50343379 GGAGTGCCGCCCGCGGCCCCGAGTCGGTCTCGAGCCGCCGGCCGGCCGTGCCGGTGTCCGTAGGC GGAGTGCCGCCCGCGGCCCCGAGTCGGTCTCGTGCCGCCGGCCGGCCGTGCCGGTGTCCGTAGGC A T PPP6R2 Ensembl:ENSG00000100239 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50343377..50343466 26863196 MeRIP-seq:(Medium) rs1209585398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707087,Human_RBP_ID_9333572,Human_RBP_ID_18423674 59413 RMVar_ID_59413 Human_SNP_ID_707124121 m1A Human chr22 + 50343531 50343531 50343531 GCCTCCACACGGGCCTCCGAAGAGCTGCCGCGACGCCCGGCCCGCAGGGCAGGTGAGTGCGGCCG GCCTCCACACGGGCCTCCGAAGAGCTGCCGCGGCGCCCGGCCCGCAGGGCAGGTGAGTGCGGCCG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:50343527..50343656 26863196 MeRIP-seq:(Medium) rs895689489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709364 Human_Splice_Rec_2180225,Human_Splice_Rec_2180269,Human_Splice_Rec_2180313,Human_Splice_Rec_2180359 59414 RMVar_ID_59414 Human_SNP_ID_707124615 m1A Human chr22 + 50345318 50345317 50345318 AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCAGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCC_GTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC CA C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50345314..50345456 26863196 MeRIP-seq:(Medium) rs1569236479 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26790023 59415 RMVar_ID_59415 Human_SNP_ID_707124616 m1A Human chr22 + 50345318 50345317 50345319 AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCAGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCC__TCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC CAG C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50345314..50345456 26863196 MeRIP-seq:(Medium) rs1569236492 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26790023 59416 RMVar_ID_59416 Human_SNP_ID_707124617 m1A Human chr22 + 50345318 50345318 50345318 AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCAGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC AGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCCGTCAGTGCCCCCTCCAGTCAGTTCCCCCCCCC A C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50345314..50345456 26863196 MeRIP-seq:(Medium) rs1356607650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26790023 59417 RMVar_ID_59417 Human_SNP_ID_707124858 m1A Human chr22 + 50346101 50346101 50346101 CCCAGTCAGTGCCCCCTCCAGTCAGTTCCCCCAGTCAGTTGCCCCCCAGTCAGTGCCCCCCAAGT CCCAGTCAGTGCCCCCTCCAGTCAGTTCCCCCCGTCAGTTGCCCCCCAGTCAGTGCCCCCCAAGT A C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50346092..50346541 26863196 MeRIP-seq:(Medium) rs1334808806 Functional Loss SNV dbSNP153 33..33 33 - - - 59418 RMVar_ID_59418 Human_SNP_ID_707125103 m1A Human chr22 + 50346670 50346667 50346670 CCCCCACCGTCAGTCAGTGCCCCTTGCAAGTCATGCTCCTCCTGTCGGTCAGTGCCTCCGCATCT CCCCCACCGTCAGTCAGTGCCCCTTGCAAG___TGCTCCTCCTGTCGGTCAGTGCCTCCGCATCT GTCA G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50346666..50346998 26863196 MeRIP-seq:(Medium) rs1168873992 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5132982,Human_RBP_ID_14529534,Human_RBP_ID_17087524,Human_RBP_ID_18953179 59419 RMVar_ID_59419 Human_SNP_ID_707125600 m1A Human chr22 - 50348582 50348582 50348582 AGCCTTGCTTTCTACTTCCAAACTGTAGTAACACCCCCAGCCCTGACACCACCCTAATTCAGCTT AGCCTTGCTTTCTACTTCCAAACTGTAGTAACGCCCCCAGCCCTGACACCACCCTAATTCAGCTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50348581..50348715 26863196 MeRIP-seq:(Medium) rs1328589278 Functional Loss SNV dbSNP153 33..33 33 - - - 59420 RMVar_ID_59420 Human_SNP_ID_707131522 m1A Human chr22 + 50367171 50367171 50367171 GGTTGAGATGTGGGAGCGGAGGATGCCTGGACAGGGGAGCAGAGGATGCCTGGACAGGGGAGCGG GGTTGAGATGTGGGAGCGGAGGATGCCTGGACGGGGGAGCAGAGGATGCCTGGACAGGGGAGCGG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50367168..50367323 26863196 MeRIP-seq:(Medium) rs958884112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215283 59421 RMVar_ID_59421 Human_SNP_ID_707135302 m1A Human chr22 - 50380100 50380094 50380100 AGCGGAAGCAGCCTGAAACTCTTACCAGAACCAGAACTGTGTCAAACCTCTTTTCCTTATAAATT AGCGGAAGCAGCCTGAAACTCTTACCAGAACC______GTGTCAAACCTCTTTTCCTTATAAATT CAGTTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50380097..50380172 26863196 MeRIP-seq:(Medium) rs940423952 Functional Loss DEL dbSNP153 33..38 33 - - - 59422 RMVar_ID_59422 Human_SNP_ID_707142814 m1A Human chr22 + 50405438 50405438 50405438 AGGCCTGGAGAGAGGTGAGAGGCCTGGCAGGCAAGTGTGAAGGCCTGGAGAGAGGTGAGAGGCCT AGGCCTGGAGAGAGGTGAGAGGCCTGGCAGGCGAGTGTGAAGGCCTGGAGAGAGGTGAGAGGCCT A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:50405121..50405583;chr22:50405102..50405607;chr22:50405092..50405608 26863196 MeRIP-seq:(Medium) rs1161987611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833077,Human_RBP_ID_17147839 RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_267402,RMVar_hsa_circ_77386,RMVar_hsa_circ_82051,RMVar_hsa_circ_61276,RMVar_hsa_circ_215286,RMVar_hsa_circ_215288,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_69050,RMVar_hsa_circ_215296,RMVar_hsa_circ_323054,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297 59423 RMVar_ID_59423 Human_SNP_ID_707143117 m1A Human chr22 + 50406272 50406272 50406272 GTGAGAGACCTGGCAGGCGAGTGTGAAGGCCTAGAGGGAGGTGAGAGGCCTGGAGAGAGGTGAGA GTGAGAGACCTGGCAGGCGAGTGTGAAGGCCTGGAGGGAGGTGAGAGGCCTGGAGAGAGGTGAGA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50405701..50406453;chr22:50405690..50406485 26863196 MeRIP-seq:(Medium) rs1448145445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833082,Human_RBP_ID_17148839 RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_267402,RMVar_hsa_circ_77386,RMVar_hsa_circ_82051,RMVar_hsa_circ_61276,RMVar_hsa_circ_215286,RMVar_hsa_circ_215288,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_69050,RMVar_hsa_circ_215296,RMVar_hsa_circ_323054,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297 59424 RMVar_ID_59424 Human_SNP_ID_707150720 m1A Human chr22 + 50433176 50433176 50433176 AGAAGTGTCCTGGAGGAGGGCAGGGGGCGCGGACACTGGGCAGGGGCCGGGCATTTGCTCTGGAG AGAAGTGTCCTGGAGGAGGGCAGGGGGCGCGGGCACTGGGCAGGGGCCGGGCATTTGCTCTGGAG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50433172..50433250 26863196 MeRIP-seq:(Medium) rs372730759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677223,Human_RBP_ID_8119718,Human_RBP_ID_8207687,Human_RBP_ID_8729599,Human_RBP_ID_21985982,Human_RBP_ID_22725032,Human_RBP_ID_26790032 RMVar_hsa_circ_102802,RMVar_hsa_circ_77386,RMVar_hsa_circ_82051,RMVar_hsa_circ_215286,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_215297,RMVar_hsa_circ_45138,RMVar_hsa_circ_79344,RMVar_hsa_circ_215303,RMVar_hsa_circ_128190,RMVar_hsa_circ_215305 59425 RMVar_ID_59425 Human_SNP_ID_707150817 m1A Human chr22 - 50433481 50433481 50433481 GAGCAAATGCCCGGCCCCTGCCCAGCGTCCGCACCCCCAGCCCTCCTCCAGGTTCACCTCCAGGG GAGCAAATGCCCGGCCCCTGCCCAGCGTCCGCGCCCCCAGCCCTCCTCCAGGTTCACCTCCAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50433419..50433545 26863196 MeRIP-seq:(Medium) rs550107185 Functional Loss SNV dbSNP153 33..33 33 - - - 59426 RMVar_ID_59426 Human_SNP_ID_707150818 m1A Human chr22 - 50433481 50433481 50433481 GAGCAAATGCCCGGCCCCTGCCCAGCGTCCGCACCCCCAGCCCTCCTCCAGGTTCACCTCCAGGG GAGCAAATGCCCGGCCCCTGCCCAGCGTCCGCCCCCCCAGCCCTCCTCCAGGTTCACCTCCAGGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50433419..50433545 26863196 MeRIP-seq:(Medium) rs550107185 Functional Loss SNV dbSNP153 33..33 33 - - - 59427 RMVar_ID_59427 Human_SNP_ID_707150941 m1A Human chr22 - 50434183 50434183 50434183 CTCCTCCAGGTTCACCTCCAGAGCAAATGCCCAGCCCCTGCCCAGCGTCTGCGCCCCCGGCCCTC CTCCTCCAGGTTCACCTCCAGAGCAAATGCCCTGCCCCTGCCCAGCGTCTGCGCCCCCGGCCCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50434131..50434223 26863196 MeRIP-seq:(Medium) rs879061601 Functional Loss SNV dbSNP153 33..33 33 - - - 59428 RMVar_ID_59428 Human_SNP_ID_707150942 m1A Human chr22 - 50434183 50434183 50434183 CTCCTCCAGGTTCACCTCCAGAGCAAATGCCCAGCCCCTGCCCAGCGTCTGCGCCCCCGGCCCTC CTCCTCCAGGTTCACCTCCAGAGCAAATGCCCGGCCCCTGCCCAGCGTCTGCGCCCCCGGCCCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50434131..50434223 26863196 MeRIP-seq:(Medium) rs879061601 Functional Loss SNV dbSNP153 33..33 33 - - - 59429 RMVar_ID_59429 Human_SNP_ID_707151005 m1A Human chr22 - 50434437 50434437 50434437 CCGGCCCTCCTCCAGGTTCACCTCCAGAGCAAATGCCCGGCCCCTGCCCAGCGTCCGCGCCCCCG CCGGCCCTCCTCCAGGTTCACCTCCAGAGCAAGTGCCCGGCCCCTGCCCAGCGTCCGCGCCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50434425..50434511;chr22:50434424..50434520 26863196 MeRIP-seq:(Medium) rs1293535631 Functional Loss SNV dbSNP153 33..33 33 - - - 59430 RMVar_ID_59430 Human_SNP_ID_707151049 m1A Human chr22 + 50434597 50434597 50434597 CCTGGAGGTGAACCTGGAGGAGGGCCGGGGGCATGGATGCTGGGCAGGGGCCGGGCATTTGCTCT CCTGGAGGTGAACCTGGAGGAGGGCCGGGGGCGTGGATGCTGGGCAGGGGCCGGGCATTTGCTCT A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50434588..50434731 26863196 MeRIP-seq:(Medium) rs373740449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102802,RMVar_hsa_circ_77386,RMVar_hsa_circ_82051,RMVar_hsa_circ_215286,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_215297,RMVar_hsa_circ_45138,RMVar_hsa_circ_79344,RMVar_hsa_circ_215303,RMVar_hsa_circ_128190,RMVar_hsa_circ_215305 59431 RMVar_ID_59431 Human_SNP_ID_707151058 m1A Human chr22 - 50434622 50434622 50434622 GCATCCATGCCCCCGGCCCTCCTCCAGAGCAAATGCCCGGCCCCTGCCCAGCATCCATGCCCCCG GCATCCATGCCCCCGGCCCTCCTCCAGAGCAAGTGCCCGGCCCCTGCCCAGCATCCATGCCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50434609..50434731 26863196 MeRIP-seq:(Medium) rs1241268146 Functional Loss SNV dbSNP153 33..33 33 - - - 59432 RMVar_ID_59432 Human_SNP_ID_707151125 m1A Human chr22 + 50434818 50434818 50434818 GGGCCGGGCATTTGCTCTGGAGGTGAACCTGGAGGAGGGCCGGGGGCGCGGACACTGGGCAGGGG GGGCCGGGCATTTGCTCTGGAGGTGAACCTGGGGGAGGGCCGGGGGCGCGGACACTGGGCAGGGG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50434815..50434974 26863196 MeRIP-seq:(Medium) rs540443872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266372,Human_RBP_ID_3676570,Human_RBP_ID_5325094,Human_RBP_ID_5388638,Human_RBP_ID_8118712,Human_RBP_ID_8207689,Human_RBP_ID_8235729,Human_RBP_ID_8729603,Human_RBP_ID_8943240,Human_RBP_ID_9333094,Human_RBP_ID_9354245,Human_RBP_ID_9433584,Human_RBP_ID_17400086,Human_RBP_ID_18498300,Human_RBP_ID_21985309,Human_RBP_ID_22480520,Human_RBP_ID_22725033 RMVar_hsa_circ_102802,RMVar_hsa_circ_77386,RMVar_hsa_circ_82051,RMVar_hsa_circ_215286,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_215297,RMVar_hsa_circ_45138,RMVar_hsa_circ_79344,RMVar_hsa_circ_215303,RMVar_hsa_circ_128190,RMVar_hsa_circ_215305 59433 RMVar_ID_59433 Human_SNP_ID_707151141 m1A Human chr22 - 50434841 50434840 50434841 CACTTCGGAGAGCAAGTGCCCGGCCCCTGCCCAGTGTCCGCGCCCCCGGCCCTCCTCCAGGTTCA CACTTCGGAGAGCAAGTGCCCGGCCCCTGCCC_GTGTCCGCGCCCCCGGCCCTCCTCCAGGTTCA CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50434832..50434978 26863196 MeRIP-seq:(Medium) rs1440946622 Functional Loss DEL dbSNP153 33..33 33 - - - 59434 RMVar_ID_59434 Human_SNP_ID_707153647 m1A Human chr22 + 50442035 50442035 50442035 GAAGTCCTCGGGCTGGATTCCTCTAGGAGGGGACAAGGTGCCTTTCACATCTGGTGGTGCATCCC GAAGTCCTCGGGCTGGATTCCTCTAGGAGGGGGCAAGGTGCCTTTCACATCTGGTGGTGCATCCC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50442032..50442164 26863196 MeRIP-seq:(Medium) rs1025010594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22479895,Human_RBP_ID_27841194 RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 59435 RMVar_ID_59435 Human_SNP_ID_707154450 m1A Human chr22 - 50443944 50443944 50443944 GTGGTGATGGCCACAGTAGCCTCGGGGGGCACAGCCACGGCTGGGGCAGCAGTCACTTCCTTTGG GTGGTGATGGCCACAGTAGCCTCGGGGGGCACGGCCACGGCTGGGGCAGCAGTCACTTCCTTTGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:50443851..50444000 26863410 MeRIP-seq:(Medium) rs759938844 Functional Loss SNV dbSNP153 33..33 33 - - - 59436 RMVar_ID_59436 Human_SNP_ID_707154451 m1A Human chr22 - 50443944 50443944 50443944 GTGGTGATGGCCACAGTAGCCTCGGGGGGCACAGCCACGGCTGGGGCAGCAGTCACTTCCTTTGG GTGGTGATGGCCACAGTAGCCTCGGGGGGCACCGCCACGGCTGGGGCAGCAGTCACTTCCTTTGG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:50443851..50444000 26863410 MeRIP-seq:(Medium) rs759938844 Functional Loss SNV dbSNP153 33..33 33 - - - 59437 RMVar_ID_59437 Human_SNP_ID_707155400 m1A Human chr22 - 50445888 50445888 50445888 GTGGGAGGCGAGCAGCAGGTGTGGGTGAGGGGAAGGTTCTGATGACAGCTGCAGAGGCAGGGCCC GTGGGAGGCGAGCAGCAGGTGTGGGTGAGGGGTAGGTTCTGATGACAGCTGCAGAGGCAGGGCCC T A SBF1 Ensembl:ENSG00000100241 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:50445877..50446016 26863196 MeRIP-seq:(Medium) rs1384075837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677225,Human_RBP_ID_7092745,Human_RBP_ID_8207690 59438 RMVar_ID_59438 Human_SNP_ID_707155734 m1A Human chr22 - 50446466 50446466 50446466 ACAGAGGCTTGGGGGTGAAAGGGTGGGTGGTCATTTGACCCCAGAAGGCTGTTGCAGGTCCAGAG ACAGAGGCTTGGGGGTGAAAGGGTGGGTGGTCCTTTGACCCCAGAAGGCTGTTGCAGGTCCAGAG T G SBF1 Ensembl:ENSG00000100241 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50446416..50446550 26863196 MeRIP-seq:(Medium) rs1342641464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17988955 59439 RMVar_ID_59439 Human_SNP_ID_707155972 m1A Human chr22 - 50446897 50446897 50446897 TGGCCAAGGTACAGCCCGCAATGGGCCTGTAAATAGTCCGGCCCCGTCAGCGTGTGCTGGTCCAG TGGCCAAGGTACAGCCCGCAATGGGCCTGTAAGTAGTCCGGCCCCGTCAGCGTGTGCTGGTCCAG T C SBF1 Ensembl:ENSG00000100241 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50446847..50447098 32194978 MeRIP-seq:(Medium) rs1254490042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_583431,Human_RBP_ID_5119834,Human_RBP_ID_17660678,Human_RBP_ID_21896613,Human_RBP_ID_26501310 59440 RMVar_ID_59440 Human_SNP_ID_707156073 m1A Human chr22 + 50447039 50447039 50447039 GTACACACAAGTGCTGGGGGCTCGGGGCCTCAATACTGTCGAGGGCCGGGGCTGTAAACATGGCC GTACACACAAGTGCTGGGGGCTCGGGGCCTCAGTACTGTCGAGGGCCGGGGCTGTAAACATGGCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:50446972..50447239 26863196 MeRIP-seq:(Medium) rs1251901710 Functional Loss SNV dbSNP153 33..33 33 - - - 59441 RMVar_ID_59441 Human_SNP_ID_707156089 m1A Human chr22 + 50447066 50447066 50447066 CCTCAATACTGTCGAGGGCCGGGGCTGTAAACATGGCCGGGGCGGCCCTGCCCACCCCTAGTGGT CCTCAATACTGTCGAGGGCCGGGGCTGTAAACGTGGCCGGGGCGGCCCTGCCCACCCCTAGTGGT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:50447026..50447250 26863196 MeRIP-seq:(Medium) rs1053764 Functional Loss SNV dbSNP153 33..33 33 - - - 59442 RMVar_ID_59442 Human_SNP_ID_707156298 m1A Human chr22 + 50447452 50447422 50447453 ACTCTGTGTCCACACGGTGGTCGTAGTAGCGCAGCTGGAGGAGGCCACAGAGTCAGCGGAGCCCC ACT_______________________________CTGGAGGAGGCCACAGAGTCAGCGGAGCCCC TCTGTGTCCACACGGTGGTCGTAGTAGCGCAG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50447441..50447512 26863196 MeRIP-seq:(Medium) rs768726905 Functional Loss DEL dbSNP153 4..34 33 - - - 59443 RMVar_ID_59443 Human_SNP_ID_707158979 m1A Human chr22 + 50454632 50454632 50454632 CCTCCATCAGACCGTTCTTCCTCTGGGGGTTCAGGGGGCCCCTGGGCCAGTTCCCAGTCATAGGG CCTCCATCAGACCGTTCTTCCTCTGGGGGTTCGGGGGGCCCCTGGGCCAGTTCCCAGTCATAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50454503..50454680;chr22:50454489..50454671 26863196 MeRIP-seq:(Medium) rs1429349942 Functional Loss SNV dbSNP153 33..33 33 - - - 59444 RMVar_ID_59444 Human_SNP_ID_707159108 m1A Human chr22 - 50454864 50454864 50454864 GGTCTGTGTGGGAGTATGTGGACCGGCTGAGCAAGAGGACGCCTGTGTTCCACAATTACATGTAT GGTCTGTGTGGGAGTATGTGGACCGGCTGAGCTAGAGGACGCCTGTGTTCCACAATTACATGTAT T A SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50454744..50454876 26863196 MeRIP-seq:(Medium) rs199795851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930047,Human_RBP_ID_3962602,Human_RBP_ID_5601757,Human_RBP_ID_9392547,Human_RBP_ID_18169140,Human_RBP_ID_26344952 Human_Splice_Rec_2180580,Human_Splice_Rec_2180581,Human_Splice_Rec_2180658,Human_Splice_Rec_2180659,Human_Splice_Rec_2180674,Human_Splice_Rec_2180675,Human_Splice_Rec_2180692,Human_Splice_Rec_2180693 Human_miRNA_ID_2571579,Human_miRNA_ID_3045314 RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_58216,RMVar_hsa_circ_88848,RMVar_hsa_circ_215311 59445 RMVar_ID_59445 Human_SNP_ID_707159109 m1A Human chr22 - 50454864 50454864 50454864 GGTCTGTGTGGGAGTATGTGGACCGGCTGAGCAAGAGGACGCCTGTGTTCCACAATTACATGTAT GGTCTGTGTGGGAGTATGTGGACCGGCTGAGCGAGAGGACGCCTGTGTTCCACAATTACATGTAT T C SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50454744..50454876 26863196 MeRIP-seq:(Medium) rs199795851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930047,Human_RBP_ID_3962602,Human_RBP_ID_5601757,Human_RBP_ID_9392547,Human_RBP_ID_18169140,Human_RBP_ID_26344952 Human_Splice_Rec_2180580,Human_Splice_Rec_2180581,Human_Splice_Rec_2180658,Human_Splice_Rec_2180659,Human_Splice_Rec_2180674,Human_Splice_Rec_2180675,Human_Splice_Rec_2180692,Human_Splice_Rec_2180693 Human_miRNA_ID_2571579,Human_miRNA_ID_3045314 RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_58216,RMVar_hsa_circ_88848,RMVar_hsa_circ_215311 59446 RMVar_ID_59446 Human_SNP_ID_707159788 m1A Human chr22 - 50456314 50456314 50456314 TATTCGAGGCACGGCAGGTGAAGGCTAGCTTCAAGAAGCTGCTGAAAGCATGTGTCCCAGGCTGC TATTCGAGGCACGGCAGGTGAAGGCTAGCTTCTAGAAGCTGCTGAAAGCATGTGTCCCAGGCTGC T A SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50456228..50457034 32194978 MeRIP-seq:(Medium) rs1387447166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4714639,Human_RBP_ID_9127590 Human_Splice_Rec_2180572,Human_Splice_Rec_2180573,Human_Splice_Rec_2180650,Human_Splice_Rec_2180651 RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_51149,RMVar_hsa_circ_117579,RMVar_hsa_circ_88848,RMVar_hsa_circ_124178,RMVar_hsa_circ_215311,RMVar_hsa_circ_215313,RMVar_hsa_circ_82151,RMVar_hsa_circ_215314,RMVar_hsa_circ_113379,RMVar_hsa_circ_215312,RMVar_hsa_circ_108935,RMVar_hsa_circ_69950,RMVar_hsa_circ_215316,RMVar_hsa_circ_215317 59447 RMVar_ID_59447 Human_SNP_ID_707159789 m1A Human chr22 - 50456314 50456314 50456314 TATTCGAGGCACGGCAGGTGAAGGCTAGCTTCAAGAAGCTGCTGAAAGCATGTGTCCCAGGCTGC TATTCGAGGCACGGCAGGTGAAGGCTAGCTTCGAGAAGCTGCTGAAAGCATGTGTCCCAGGCTGC T C SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50456228..50457034 32194978 MeRIP-seq:(Medium) rs1387447166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4714639,Human_RBP_ID_9127590 Human_Splice_Rec_2180572,Human_Splice_Rec_2180573,Human_Splice_Rec_2180650,Human_Splice_Rec_2180651 RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_51149,RMVar_hsa_circ_117579,RMVar_hsa_circ_88848,RMVar_hsa_circ_124178,RMVar_hsa_circ_215311,RMVar_hsa_circ_215313,RMVar_hsa_circ_82151,RMVar_hsa_circ_215314,RMVar_hsa_circ_113379,RMVar_hsa_circ_215312,RMVar_hsa_circ_108935,RMVar_hsa_circ_69950,RMVar_hsa_circ_215316,RMVar_hsa_circ_215317 59448 RMVar_ID_59448 Human_SNP_ID_707160263 m1A Human chr22 - 50457070 50457070 50457070 CCAGAGCCAGGGTCACCACGCTGTCCAACCCCATGGCGGCCTCGGCCTCCAGACGGACCGCACCC CCAGAGCCAGGGTCACCACGCTGTCCAACCCCGTGGCGGCCTCGGCCTCCAGACGGACCGCACCC T C SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50456902..50457154 26863196 MeRIP-seq:(Medium) rs1373699189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19112494 Human_Splice_Rec_2180568,Human_Splice_Rec_2180569,Human_Splice_Rec_2180707 RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_51149,RMVar_hsa_circ_117579,RMVar_hsa_circ_88848,RMVar_hsa_circ_124178,RMVar_hsa_circ_215311,RMVar_hsa_circ_215313,RMVar_hsa_circ_82151,RMVar_hsa_circ_215314,RMVar_hsa_circ_113379,RMVar_hsa_circ_215312,RMVar_hsa_circ_69950,RMVar_hsa_circ_215317 59449 RMVar_ID_59449 Human_SNP_ID_707161985 m1A Human chr22 + 50460711 50460710 50460711 ACCCCACCTCCTCGTCAAAGGCCATTTTCAGCAGCTGTGTCAGTAAAAGCAGCCCTTAGGGGTGT ACCCCACCTCCTCGTCAAAGGCCATTTTCAGC_GCTGTGTCAGTAAAAGCAGCCCTTAGGGGTGT CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50460538..50461975 32194978 MeRIP-seq:(Medium) rs749194680 Functional Loss DEL dbSNP153 33..33 33 - - - 59450 RMVar_ID_59450 Human_SNP_ID_707162701 m1A Human chr22 - 50462072 50462072 50462072 GGCCGAGAGCTATGACACGGAGAGCGGCTTCGAGGATGCAGAGACCTGCGACGTAGCTGGGGCTG GGCCGAGAGCTATGACACGGAGAGCGGCTTCGTGGATGCAGAGACCTGCGACGTAGCTGGGGCTG T A SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50461962..50462074 26863196 MeRIP-seq:(Medium) rs1353498552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2180550,Human_Splice_Rec_2180630 RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_51149,RMVar_hsa_circ_117579,RMVar_hsa_circ_124178,RMVar_hsa_circ_215313,RMVar_hsa_circ_215314,RMVar_hsa_circ_113379,RMVar_hsa_circ_215317,RMVar_hsa_circ_120534,RMVar_hsa_circ_215319,RMVar_hsa_circ_95079,RMVar_hsa_circ_104496,RMVar_hsa_circ_114771,RMVar_hsa_circ_215321,RMVar_hsa_circ_215322,RMVar_hsa_circ_79620,RMVar_hsa_circ_215323,RMVar_hsa_circ_83798,RMVar_hsa_circ_100026,RMVar_hsa_circ_121913,RMVar_hsa_circ_215324,RMVar_hsa_circ_88919,RMVar_hsa_circ_215326,RMVar_hsa_circ_215328,RMVar_hsa_circ_79115,RMVar_hsa_circ_215329,RMVar_hsa_circ_215327,RMVar_hsa_circ_215325 59451 RMVar_ID_59451 Human_SNP_ID_707163989 m1A Human chr22 + 50464632 50464632 50464632 TCTTGGCTGCAGCCTGGTCCACGATCCACTGCACGGTGCCCTCATCCAGCCGGGGGAAGGGTCGG TCTTGGCTGCAGCCTGGTCCACGATCCACTGCCCGGTGCCCTCATCCAGCCGGGGGAAGGGTCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50464581..50464852 26863196 MeRIP-seq:(Medium) rs878969930 Functional Loss SNV dbSNP153 33..33 33 - - - 59452 RMVar_ID_59452 Human_SNP_ID_707164060 m1A Human chr22 - 50464742 50464742 50464742 CTGGGCCCCTGCCCCACACCTGCCGTCTCCCCACAGGAGAACCCGTACCCAGCCGTGGCGATGCA CTGGGCCCCTGCCCCACACCTGCCGTCTCCCCGCAGGAGAACCCGTACCCAGCCGTGGCGATGCA T C SBF1 Ensembl:ENSG00000100241 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50464741..50464827 26863196 MeRIP-seq:(Medium) rs992958690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22551247 RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215309,RMVar_hsa_circ_112381,RMVar_hsa_circ_215310,RMVar_hsa_circ_51149,RMVar_hsa_circ_117579,RMVar_hsa_circ_215314,RMVar_hsa_circ_113379,RMVar_hsa_circ_215317,RMVar_hsa_circ_120534,RMVar_hsa_circ_215319,RMVar_hsa_circ_69808,RMVar_hsa_circ_95079,RMVar_hsa_circ_104496,RMVar_hsa_circ_215321,RMVar_hsa_circ_79620,RMVar_hsa_circ_215323,RMVar_hsa_circ_83798,RMVar_hsa_circ_215324,RMVar_hsa_circ_88919,RMVar_hsa_circ_215328,RMVar_hsa_circ_79115,RMVar_hsa_circ_215329,RMVar_hsa_circ_215327,RMVar_hsa_circ_120017,RMVar_hsa_circ_215332,RMVar_hsa_circ_77640,RMVar_hsa_circ_215331 59453 RMVar_ID_59453 Human_SNP_ID_707165516 m1A Human chr22 - 50467652 50467652 50467652 ACGCGCGTGGAGGATGCCACAGAGAGGGAGGAAGAGGGGGATGAGGGAGGCCAGACCCACCTGTC ACGCGCGTGGAGGATGCCACAGAGAGGGAGGACGAGGGGGATGAGGGAGGCCAGACCCACCTGTC T G SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50467601..50467700 32194978 MeRIP-seq:(Medium) rs1050868430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2180518,Human_Splice_Rec_2180598 RMVar_hsa_circ_69808,RMVar_hsa_circ_77420,RMVar_hsa_circ_215333,RMVar_hsa_circ_62196,RMVar_hsa_circ_45499,RMVar_hsa_circ_28528 59454 RMVar_ID_59454 Human_SNP_ID_707165917 m1A Human chr22 - 50468446 50468446 50468446 CCTGTTCTTGTCCTCAGGGAGTGGGGAAGGCCAGGGCCAGATTCTGCAGCGCTTCCCAGAGAAGG CCTGTTCTTGTCCTCAGGGAGTGGGGAAGGCCGGGGCCAGATTCTGCAGCGCTTCCCAGAGAAGG T C SBF1 Ensembl:ENSG00000100241 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50468399..50474924 32194978 MeRIP-seq:(Medium) rs904638475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707453,Human_RBP_ID_18792476 Human_Splice_Rec_2180514,Human_Splice_Rec_2180515,Human_Splice_Rec_2180594,Human_Splice_Rec_2180595,Human_Splice_Rec_2180714,Human_Splice_Rec_2180715 RMVar_hsa_circ_69808,RMVar_hsa_circ_8896 59455 RMVar_ID_59455 Human_SNP_ID_707167458 m1A Human chr22 + 50473136 50473136 50473136 TGCCTCTTCTCTCTGCCTACCTTCAACTCCTCACCCCACGGCCACCACGCCTCCCACCTGGCCTT TGCCTCTTCTCTCTGCCTACCTTCAACTCCTCTCCCCACGGCCACCACGCCTCCCACCTGGCCTT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50473133..50473308 26863196 MeRIP-seq:(Medium) rs1456619022 Functional Loss SNV dbSNP153 33..33 33 - - - 59456 RMVar_ID_59456 Human_SNP_ID_707167859 m1A Human chr22 + 50474130 50474130 50474130 CACAGACCTCCTGGGCATGGGCACCGACCGCCACGCTGATACCCCACCCAGGGCTTGGCGTGCAG CACAGACCTCCTGGGCATGGGCACCGACCGCCCCGCTGATACCCCACCCAGGGCTTGGCGTGCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50474127..50474768 26863196 MeRIP-seq:(Medium) rs767723179 Functional Loss SNV dbSNP153 33..33 33 - - - 59457 RMVar_ID_59457 Human_SNP_ID_707168228 m1A Human chr22 + 50474864 50474864 50474864 CCGCGCCATGGCGAGGGACGCGGGGCGGCCCGAGGGGCGCGGGCGGGCTCCGCGGCTCGGGGACT CCGCGCCATGGCGAGGGACGCGGGGCGGCCCGTGGGGCGCGGGCGGGCTCCGCGGCTCGGGGACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:50474021..50475000;chr22:50474826..50474967 26863196 MeRIP-seq:(Medium) rs1403315352 Functional Loss SNV dbSNP153 33..33 33 - - - 59458 RMVar_ID_59458 Human_SNP_ID_707168260 m1A Human chr22 + 50474934 50474928 50474934 ACGGCGCGCTCATGGCCCGGCCCCGGCCCTGGACCGCGCACCCCGGACACCCCTGGTTCGCTCCG ACGGCGCGCTCATGGCCCGGCCCCGGC______CCGCGCACCCCGGACACCCCTGGTTCGCTCCG CCCTGGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:50474845..50474991 26863410 MeRIP-seq:(Medium) rs1272780197 Functional Loss DEL dbSNP153 28..33 33 - - - 59459 RMVar_ID_59459 Human_SNP_ID_707170406 m1A Human chr22 + 50481660 50481642 50481660 CCGCCTTGCGCCCCGGACCCGCGGCCGACCCCAGACCCGCTGCCCGCTTCGCGCCCGAGGCCTGC CCGCCTTGCGCCCCG__________________GACCCGCTGCCCGCTTCGCGCCCGAGGCCTGC GGACCCGCGGCCGACCCCA G ADM2 Ensembl:ENSG00000128165 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:50481576..50481825 26863410 MeRIP-seq:(Medium) rs1320021266 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_782351 59460 RMVar_ID_59460 Human_SNP_ID_707170413 m1A Human chr22 + 50481660 50481660 50481660 CCGCCTTGCGCCCCGGACCCGCGGCCGACCCCAGACCCGCTGCCCGCTTCGCGCCCGAGGCCTGC CCGCCTTGCGCCCCGGACCCGCGGCCGACCCCGGACCCGCTGCCCGCTTCGCGCCCGAGGCCTGC A G ADM2 Ensembl:ENSG00000128165 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:50481576..50481825 26863410 MeRIP-seq:(Medium) rs1158846088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782351 59461 RMVar_ID_59461 Human_SNP_ID_707178507 m1A Human chr22 + 50503057 50503056 50503057 ATGACAGTGCTTCCCCTCTTCCCCTGGGAGTCAGCCTCTTCCCCTCTGGCACGGGGCCTAGGGTT ATGACAGTGCTTCCCCTCTTCCCCTGGGAGTC_GCCTCTTCCCCTCTGGCACGGGGCCTAGGGTT CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50503007..50503104 26863196 MeRIP-seq:(Medium) rs1345488800 Functional Loss DEL dbSNP153 33..33 33 - - - 59462 RMVar_ID_59462 Human_SNP_ID_707179029 m1A Human chr22 - 50503906 50503906 50503906 GCCTCCAGCTTCTGAACATCGGGTCCTGCTGCAGCCAGTGGTGGCGGCGCCAGTGGGTGGAGGAG GCCTCCAGCTTCTGAACATCGGGTCCTGCTGCTGCCAGTGGTGGCGGCGCCAGTGGGTGGAGGAG T A LMF2 Ensembl:ENSG00000100258 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50503879..50504043;chr22:50503879..50504046 26863196 MeRIP-seq:(Medium) rs766166819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2180817,Human_Splice_Rec_2180841,Human_Splice_Rec_2180851 RMVar_hsa_circ_98001,RMVar_hsa_circ_108211,RMVar_hsa_circ_113377,RMVar_hsa_circ_125210,RMVar_hsa_circ_112969,RMVar_hsa_circ_106066,RMVar_hsa_circ_107094,RMVar_hsa_circ_103119,RMVar_hsa_circ_215343,RMVar_hsa_circ_215345,RMVar_hsa_circ_215347,RMVar_hsa_circ_215348,RMVar_hsa_circ_215346,RMVar_hsa_circ_215344,RMVar_hsa_circ_215341,RMVar_hsa_circ_215342,RMVar_hsa_circ_109376,RMVar_hsa_circ_215350 59463 RMVar_ID_59463 Human_SNP_ID_707179421 m1A Human chr22 - 50504422 50504422 50504422 CAGTGATCCGCCTTGTCCAGAGCCAAGTGGCCAGGTATCCCTTCCACAAGCAGCCGCCCACCTAC CAGTGATCCGCCTTGTCCAGAGCCAAGTGGCCGGGTATCCCTTCCACAAGCAGCCGCCCACCTAC T C LMF2 Ensembl:ENSG00000100258 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50504351..50504425 32194978 MeRIP-seq:(Medium) rs752140596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10865,Human_RBP_ID_65155,Human_RBP_ID_780876,Human_RBP_ID_929662,Human_RBP_ID_3962623,Human_RBP_ID_5119977,Human_RBP_ID_5387512,Human_RBP_ID_19113890,Human_RBP_ID_27841326 Human_Splice_Rec_2180814,Human_Splice_Rec_2180815,Human_Splice_Rec_2180838,Human_Splice_Rec_2180839,Human_Splice_Rec_2180849 Human_miRNA_ID_2676414,Human_miRNA_ID_2927168 RMVar_hsa_circ_98001,RMVar_hsa_circ_108211,RMVar_hsa_circ_113377,RMVar_hsa_circ_125210,RMVar_hsa_circ_112969,RMVar_hsa_circ_106066,RMVar_hsa_circ_107094,RMVar_hsa_circ_103119,RMVar_hsa_circ_215343,RMVar_hsa_circ_215345,RMVar_hsa_circ_215347,RMVar_hsa_circ_215348,RMVar_hsa_circ_215346,RMVar_hsa_circ_215344,RMVar_hsa_circ_215341,RMVar_hsa_circ_215342,RMVar_hsa_circ_109376,RMVar_hsa_circ_215350 59464 RMVar_ID_59464 Human_SNP_ID_707179665 m1A Human chr22 - 50504715 50504715 50504715 GACCTCGGCCTGCCTGGCAGGAGATCGAGTTCATGTACAAGCCTGGGAACCTGAGCCGGCCGCCC GACCTCGGCCTGCCTGGCAGGAGATCGAGTTCGTGTACAAGCCTGGGAACCTGAGCCGGCCGCCC T C LMF2 Ensembl:ENSG00000100258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50504558..50504729 26863196 MeRIP-seq:(Medium) rs773156059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707505,Human_RBP_ID_27821793 Human_Splice_Rec_2180812,Human_Splice_Rec_2180836,Human_Splice_Rec_2180848 Human_miRNA_ID_2730387 RMVar_hsa_circ_98001,RMVar_hsa_circ_108211,RMVar_hsa_circ_113377,RMVar_hsa_circ_125210,RMVar_hsa_circ_112969,RMVar_hsa_circ_106066,RMVar_hsa_circ_107094,RMVar_hsa_circ_103119,RMVar_hsa_circ_116312,RMVar_hsa_circ_215343,RMVar_hsa_circ_215345,RMVar_hsa_circ_215347,RMVar_hsa_circ_215348,RMVar_hsa_circ_215346,RMVar_hsa_circ_215344,RMVar_hsa_circ_215341,RMVar_hsa_circ_215342,RMVar_hsa_circ_109376,RMVar_hsa_circ_215350,RMVar_hsa_circ_215351,RMVar_hsa_circ_87279,RMVar_hsa_circ_92702,RMVar_hsa_circ_215352,RMVar_hsa_circ_215353 59465 RMVar_ID_59465 Human_SNP_ID_707179666 m1A Human chr22 - 50504715 50504715 50504715 GACCTCGGCCTGCCTGGCAGGAGATCGAGTTCATGTACAAGCCTGGGAACCTGAGCCGGCCGCCC GACCTCGGCCTGCCTGGCAGGAGATCGAGTTCCTGTACAAGCCTGGGAACCTGAGCCGGCCGCCC T G LMF2 Ensembl:ENSG00000100258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50504558..50504729 26863196 MeRIP-seq:(Medium) rs773156059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707505,Human_RBP_ID_27821793 Human_Splice_Rec_2180812,Human_Splice_Rec_2180836,Human_Splice_Rec_2180848 Human_miRNA_ID_2730387 RMVar_hsa_circ_98001,RMVar_hsa_circ_108211,RMVar_hsa_circ_113377,RMVar_hsa_circ_125210,RMVar_hsa_circ_112969,RMVar_hsa_circ_106066,RMVar_hsa_circ_107094,RMVar_hsa_circ_103119,RMVar_hsa_circ_116312,RMVar_hsa_circ_215343,RMVar_hsa_circ_215345,RMVar_hsa_circ_215347,RMVar_hsa_circ_215348,RMVar_hsa_circ_215346,RMVar_hsa_circ_215344,RMVar_hsa_circ_215341,RMVar_hsa_circ_215342,RMVar_hsa_circ_109376,RMVar_hsa_circ_215350,RMVar_hsa_circ_215351,RMVar_hsa_circ_87279,RMVar_hsa_circ_92702,RMVar_hsa_circ_215352,RMVar_hsa_circ_215353 59466 RMVar_ID_59466 Human_SNP_ID_707180388 m1A Human chr22 + 50505751 50505751 50505751 GGTGCTGGTCGTCCAGCAGCGCAGTGGTAAGCACCAGCGTCATCAGGTTGAAGAAGTTGTAGTTG GGTGCTGGTCGTCCAGCAGCGCAGTGGTAAGCGCCAGCGTCATCAGGTTGAAGAAGTTGTAGTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50505674..50505756 26863196 MeRIP-seq:(Medium) rs1340957791 Functional Loss SNV dbSNP153 33..33 33 - - - 59467 RMVar_ID_59467 Human_SNP_ID_707180843 m1A Human chr22 + 50506452 50506445 50506452 GGGGGGCCTCCTTGCGGTGGGAGGCTGGCCTCAGCGGGGCCACCAGCACGGCCAGGAAGCCAGTC GGGGGGCCTCCTTGCGGTGGGAGGCT_______GCGGGGCCACCAGCACGGCCAGGAAGCCAGTC TGGCCTCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50506401..50506475 32194978 MeRIP-seq:(Medium) rs1569518735 Functional Loss DEL dbSNP153 27..33 33 - - - 59468 RMVar_ID_59468 Human_SNP_ID_707181245 m1A Human chr22 - 50507065 50507065 50507065 CTCAGAGGTAGTCTAGTCTGCAAGGGCTGTCCAGGGCCTGGCCATGACATGCCCTCCCACAGGCC CTCAGAGGTAGTCTAGTCTGCAAGGGCTGTCCGGGGCCTGGCCATGACATGCCCTCCCACAGGCC T C LMF2 Ensembl:ENSG00000100258 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50507015..50507102 26863196 MeRIP-seq:(Medium) rs774227067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5388699,Human_RBP_ID_21985671 Human_Splice_Rec_2180820 Human_miRNA_ID_2510058 RMVar_hsa_circ_125210,RMVar_hsa_circ_215341,RMVar_hsa_circ_87279,RMVar_hsa_circ_215353 59469 RMVar_ID_59469 Human_SNP_ID_707181847 m1A Human chr22 + 50508279 50508279 50508279 AAAATGGCGCCAGAACTAGTGGCGGGCTGAGGACGCCGTACCCCTCGGAAGGCAGCCCTGCGGTC AAAATGGCGCCAGAACTAGTGGCGGGCTGAGGGCGCCGTACCCCTCGGAAGGCAGCCCTGCGGTC A G NCAPH2 Ensembl:ENSG00000025770 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:50508226..50508450 26863196 MeRIP-seq:(Medium) rs111442842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_308318 RMVar_hsa_circ_13053 59470 RMVar_ID_59470 Human_SNP_ID_707181853 m1A Human chr22 + 50508286 50508286 50508286 CGCCAGAACTAGTGGCGGGCTGAGGACGCCGTACCCCTCGGAAGGCAGCCCTGCGGTCCCTTTGC CGCCAGAACTAGTGGCGGGCTGAGGACGCCGTGCCCCTCGGAAGGCAGCCCTGCGGTCCCTTTGC A G NCAPH2 Ensembl:ENSG00000025770 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:50508226..50508450;chr22:50508226..50508463;chr22:50508226..50508425 26863196 MeRIP-seq:(Medium) rs1229247632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27310730 RMVar_hsa_circ_13053 59471 RMVar_ID_59471 Human_SNP_ID_707184348 m1A Human chr22 - 50515783 50515783 50515783 TACATTCAAATGTCCCCAAACACTTTACTTCCATACTTTACCCAACATCTTCCCCAACGCTGGCT TACATTCAAATGTCCCCAAACACTTTACTTCCGTACTTTACCCAACATCTTCCCCAACGCTGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50515781..50515983 26863196 MeRIP-seq:(Medium) rs183242642 Functional Loss SNV dbSNP153 33..33 33 - - - 59472 RMVar_ID_59472 Human_SNP_ID_707184365 m1A Human chr22 - 50515819 50515818 50515820 TTAGCTCTGGGGCTGCATTCATAGCTGTCCACAGAGTACATTCAAATGTCCCCAAACACTTTACT TTAGCTCTGGGGCTGCATTCATAGCTGTCCA__GAGTACATTCAAATGTCCCCAAACACTTTACT CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:50515811..50515969 26863196 MeRIP-seq:(Medium) rs1393955425 Functional Loss DEL dbSNP153 32..33 33 - - - 59473 RMVar_ID_59473 Human_SNP_ID_707185619 m1A Human chr22 + 50519210 50519210 50519210 CTCCCTGCCTAGGCCCCTCTCCAGAAGGCCCGATGCCCCTGGGTGGGGGCGAGGACGAGGATGCA CTCCCTGCCTAGGCCCCTCTCCAGAAGGCCCGCTGCCCCTGGGTGGGGGCGAGGACGAGGATGCA A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cells, overexperss TRMT6;HTR8/Svneo,Hypoxia IP chr22:50519201..50519300 29072297,32194978 m1A-MAP:(High) rs763292905 Functional Loss SNV dbSNP153 33..33 33 - - - 59474 RMVar_ID_59474 Human_SNP_ID_707186731 m1A Human chr22 - 50522184 50522184 50522184 GCTCCTTCACGTGTGTCCAGTACAGGACCTCCATGTCTGCAGACAAAGGCCTTGTGAGGGCTCCC GCTCCTTCACGTGTGTCCAGTACAGGACCTCCGTGTCTGCAGACAAAGGCCTTGTGAGGGCTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50522176..50522200 26863196 MeRIP-seq:(Medium) rs1466866312 Functional Loss SNV dbSNP153 33..33 33 - - - 59475 RMVar_ID_59475 Human_SNP_ID_707186795 m1A Human chr22 - 50522327 50522327 50522327 AGCCACTGCTCAGCCACCTGTCCAGAGAAAGCATCTGTGAGGGGCACTGTCACCTCCCATCAGGG AGCCACTGCTCAGCCACCTGTCCAGAGAAAGCGTCTGTGAGGGGCACTGTCACCTCCCATCAGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50522326..50522350 26863196 MeRIP-seq:(Medium) rs368746090 Functional Loss SNV dbSNP153 33..33 33 - - - 59476 RMVar_ID_59476 Human_SNP_ID_707186959 m1A Human chr22 + 50522653 50522653 50522653 GGGGAGAGCGTGGCCCCTTAGCTGCCCAGCTCACAGCTACCCCTTCCCAGACGCAGTGCCGATGT GGGGAGAGCGTGGCCCCTTAGCTGCCCAGCTCTCAGCTACCCCTTCCCAGACGCAGTGCCGATGT A T NCAPH2 Ensembl:ENSG00000025770 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50522651..50522725 26863196 MeRIP-seq:(Medium) rs1462113151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2180899,Human_Splice_Rec_2180951,Human_Splice_Rec_2181025,Human_Splice_Rec_2181053 RMVar_hsa_circ_103549,RMVar_hsa_circ_118868,RMVar_hsa_circ_215361,RMVar_hsa_circ_117956,RMVar_hsa_circ_215363,RMVar_hsa_circ_105691,RMVar_hsa_circ_215364,RMVar_hsa_circ_215365 59477 RMVar_ID_59477 Human_SNP_ID_707187081 m1A Human chr22 - 50522907 50522907 50522907 CAGCGGCCCCGCCTCACCTGCTCCTGGAGCAGAGGCTGCACTGTGTCCTCCCAGTCCCTGATGCG CAGCGGCCCCGCCTCACCTGCTCCTGGAGCAGGGGCTGCACTGTGTCCTCCCAGTCCCTGATGCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:50522826..50522925 32194978 MeRIP-seq:(Medium) rs748946438 Functional Loss SNV dbSNP153 33..33 33 - - - 59478 RMVar_ID_59478 Human_SNP_ID_707188208 m1A Human chr22 - 50525049 50525038 50525049 GGGAAAGGCTCAAAGGTCACCAACGCAAAGGCAGGGCGTCGGCTGTGAGCCCGGAGGAGCTGCTG GGGAAAGGCTCAAAGGTCACCAACGCAAAGGC___________TGTGAGCCCGGAGGAGCTGCTG AGCCGACGCCCT A SCO2 Ensembl:ENSG00000284194 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50524817..50525176 26863196 MeRIP-seq:(Medium) rs1205181658 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_23954533 59479 RMVar_ID_59479 Human_SNP_ID_707188675 m1A Human chr22 + 50525835 50525835 50525835 GGGCGAGGGGGCGGCGAATGGCGCGCGGTCGGAGAGTACGAGCGCCTCCTGCAGGGCGCGGCTCT GGGCGAGGGGGCGGCGAATGGCGCGCGGTCGGCGAGTACGAGCGCCTCCTGCAGGGCGCGGCTCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50525784..50526428 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 59480 RMVar_ID_59480 Human_SNP_ID_707189422 m1A Human chr22 + 50526939 50526939 50526939 GGGCCAGGAGGAACTTGTACTTGGTCTGGGGCAGGAACGCCACAGAGGGCTTCCCCAGGTCCAGG GGGCCAGGAGGAACTTGTACTTGGTCTGGGGCGGGAACGCCACAGAGGGCTTCCCCAGGTCCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50526902..50526973 26863196 MeRIP-seq:(Medium) rs1317226550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14531795 59481 RMVar_ID_59481 Human_SNP_ID_707190557 m1A Human chr22 + 50529564 50529564 50529564 CGGCCACGAAGCCCCTGATGTCCGCTTCGCTCAGGCGGCCTCCGTCTCGCTTCATGCGGATCAGC CGGCCACGAAGCCCCTGATGTCCGCTTCGCTCCGGCGGCCTCCGTCTCGCTTCATGCGGATCAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50529516..50529593 26863196 MeRIP-seq:(Medium) rs1064792857 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_197 59482 RMVar_ID_59482 Human_SNP_ID_707190558 m1A Human chr22 + 50529564 50529564 50529564 CGGCCACGAAGCCCCTGATGTCCGCTTCGCTCAGGCGGCCTCCGTCTCGCTTCATGCGGATCAGC CGGCCACGAAGCCCCTGATGTCCGCTTCGCTCTGGCGGCCTCCGTCTCGCTTCATGCGGATCAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50529516..50529593 26863196 MeRIP-seq:(Medium) rs1064792857 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_197 59483 RMVar_ID_59483 Human_SNP_ID_707190635 m1A Human chr22 - 50529713 50529713 50529713 CCCGGACGTGTCAGGCATCCCCGCAGGCCCGGAGCGATGGCAGCCTTGATGACCCCGGGAACCGG CCCGGACGTGTCAGGCATCCCCGCAGGCCCGGGGCGATGGCAGCCTTGATGACCCCGGGAACCGG T C TYMP,ODF3B Ensembl:ENSG00000025708,Ensembl:ENSG00000177989 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50529674..50530000 26863196 MeRIP-seq:(Medium) rs571316178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2181072,Human_Splice_Rec_2181090,Human_Splice_Rec_2181108,Human_Splice_Rec_2181142,Human_Splice_Rec_2181160,Human_Splice_Rec_2181174,Human_Splice_Rec_2181200,Human_Splice_Rec_2181228,Human_Splice_Rec_2181236,Human_Splice_Rec_2181238,Human_Splice_Rec_2181242 59484 RMVar_ID_59484 Human_SNP_ID_707190950 m1A Human chr22 - 50530473 50530459 50530473 CGCTGGTGACCGACGCGGACAACTGACCCGCCAGGCGGGAGCGGCCCCACACGTGTTTGCTTAAA CGCTGGTGACCGACGCGGACAACTGACCCGCC______________CCACACGTGTTTGCTTAAA GGGCCGCTCCCGCCT G ODF3B Ensembl:ENSG00000177989 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50530435..50530694 26863196 MeRIP-seq:(Medium) rs781283572 Functional Loss DEL dbSNP153 33..46 33 - - - Human_Splice_Rec_2181250,Human_Splice_Rec_2181260,Human_Splice_Rec_2181272,Human_Splice_Rec_2181280,Human_Splice_Rec_2181290,Human_Splice_Rec_2181300 59485 RMVar_ID_59485 Human_SNP_ID_707191571 m1A Human chr22 + 50531693 50531693 50531693 AGCGGGCACCAGGTGGCCTGGCCCGGGGCCGCACGTCGTCTGCTGCGTGGGGAAGCGCGCGCCGA AGCGGGCACCAGGTGGCCTGGCCCGGGGCCGCTCGTCGTCTGCTGCGTGGGGAAGCGCGCGCCGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50531642..50531752 26863196 MeRIP-seq:(Medium) rs1248841227 Functional Loss SNV dbSNP153 33..33 33 - - - 59486 RMVar_ID_59486 Human_SNP_ID_707196172 m1A Human chr22 + 50548047 50547999 50548047 CATCCCCTGCCCCAGCCCCCACCTCAGCCCCAACCCCAACCCCAGCCGCATCCCCTGCCCCAGCT _________________________________CCCCAACCCCAGCCGCATCCCCTGCCCCAGCT GCCCCAACCCCAGCCGCATCCCCTGCCCCAGCCCCCACCTCAGCCCCAA G KLHDC7B Ensembl:ENSG00000130487 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50548000..50548071 26863196 MeRIP-seq:(Medium) rs758283899 Functional Loss DEL dbSNP153 1..33 33 - - - 59487 RMVar_ID_59487 Human_SNP_ID_707196202 m1A Human chr22 + 50548047 50548047 50548047 CATCCCCTGCCCCAGCCCCCACCTCAGCCCCAACCCCAACCCCAGCCGCATCCCCTGCCCCAGCT CATCCCCTGCCCCAGCCCCCACCTCAGCCCCAGCCCCAACCCCAGCCGCATCCCCTGCCCCAGCT A G KLHDC7B Ensembl:ENSG00000130487 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50548000..50548071 26863196 MeRIP-seq:(Medium) rs558432431 Functional Loss SNV dbSNP153 33..33 33 - - - 59488 RMVar_ID_59488 Human_SNP_ID_707206867 m1A Human chr22 - 50582588 50582588 50582588 GGAGTACTTGGGCGGGGCCTGGCGCCGAGTGCAGCCCGAGGAGCTGAGGGTTTACCCCGTGAGGT GGAGTACTTGGGCGGGGCCTGGCGCCGAGTGCGGCCCGAGGAGCTGAGGGTTTACCCCGTGAGGT T C CHKB-CPT1B,CHKB Ensembl:ENSG00000254413,Ensembl:ENSG00000100288 Protein coding,Protein coding exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50582367..50582965 26863196 MeRIP-seq:(Medium) rs1197978216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707725,Human_RBP_ID_5389812,Human_RBP_ID_18792563,Human_RBP_ID_19008402,Human_RBP_ID_26771025 Human_Splice_Rec_2181697,Human_Splice_Rec_2181715 59489 RMVar_ID_59489 Human_SNP_ID_707206868 m1A Human chr22 - 50582588 50582588 50582588 GGAGTACTTGGGCGGGGCCTGGCGCCGAGTGCAGCCCGAGGAGCTGAGGGTTTACCCCGTGAGGT GGAGTACTTGGGCGGGGCCTGGCGCCGAGTGCCGCCCGAGGAGCTGAGGGTTTACCCCGTGAGGT T G CHKB-CPT1B,CHKB Ensembl:ENSG00000254413,Ensembl:ENSG00000100288 Protein coding,Protein coding exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50582367..50582965 26863196 MeRIP-seq:(Medium) rs1197978216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4707725,Human_RBP_ID_5389812,Human_RBP_ID_18792563,Human_RBP_ID_19008402,Human_RBP_ID_26771025 Human_Splice_Rec_2181697,Human_Splice_Rec_2181715 59490 RMVar_ID_59490 Human_SNP_ID_707213705 m1A Human chr22 + 50604750 50604750 50604750 AGAGGACGACGAGGAAGAGGAGGATGCCGAGGACAGTGCGGGGTCCCCCGGGGGCAGGGGCACGG AGAGGACGACGAGGAAGAGGAGGATGCCGAGGGCAGTGCGGGGTCCCCCGGGGGCAGGGGCACGG A G MAPK8IP2 Ensembl:ENSG00000008735 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50604715..50604911 26863196 MeRIP-seq:(Medium) rs1305958060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40251 59491 RMVar_ID_59491 Human_SNP_ID_707215122 m1A Human chr22 + 50608688 50608688 50608688 CAGCGGGCAGGGGCGCAGACCAGACAGCAGGGACAGCTCTGGGGTGGAGAGGTGGGACAGTGGGC CAGCGGGCAGGGGCGCAGACCAGACAGCAGGGCCAGCTCTGGGGTGGAGAGGTGGGACAGTGGGC A C MAPK8IP2 Ensembl:ENSG00000008735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50608668..50608878;chr22:50608577..50608816 26863196 MeRIP-seq:(Medium) rs369468729 Functional Loss SNV dbSNP153 33..33 33 - - - 59492 RMVar_ID_59492 Human_SNP_ID_707219677 m1A Human chr22 - 50624132 50624132 50624132 GGGAGGCGGTGGTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGAAA GGGAGGCGGTGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAGAGAAA T C ARSA Ensembl:ENSG00000100299 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1395424621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 59493 RMVar_ID_59493 Human_SNP_ID_707248639 m1A Human chr22 + 50720968 50720968 50720968 ATCGAGGGCAGCGCCCCCGGCGCGGATCTGCCATCCCTACAGCCCTCCCGCTCCATCGACGAGCG ATCGAGGGCAGCGCCCCCGGCGCGGATCTGCCGTCCCTACAGCCCTCCCGCTCCATCGACGAGCG A G SHANK3 Ensembl:ENSG00000251322 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:50720767..50721058 26863196 MeRIP-seq:(Medium) rs767307442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268566,RMVar_hsa_circ_61556,RMVar_hsa_circ_215372,RMVar_hsa_circ_350961 59494 RMVar_ID_59494 Human_SNP_ID_707250988 m1A Human chr22 + 50727948 50727948 50727948 AGTATCATGTGTTAGAGGGTGGGTGGCCCAGAAGCTCTCTGGGAGGCTGGCAGGTGCTGTGATGT AGTATCATGTGTTAGAGGGTGGGTGGCCCAGACGCTCTCTGGGAGGCTGGCAGGTGCTGTGATGT A C SHANK3 Ensembl:ENSG00000251322 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50727682..50728073 26863196 MeRIP-seq:(Medium) rs979539667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5149600,Human_RBP_ID_5204136,Human_RBP_ID_8207728,Human_RBP_ID_18464100 59495 RMVar_ID_59495 Human_SNP_ID_707262897 m1A Human chr22 + 50769344 50769344 50769344 ATCAGCTCCTCCCCTCCCTGCCACCCATGCCCATGCACTGTCCCGGTTCTCTCCATCACACCTGC ATCAGCTCCTCCCCTCCCTGCCACCCATGCCCGTGCACTGTCCCGGTTCTCTCCATCACACCTGC A G RPL23AP82 Ensembl:ENSG00000184319 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:50769296..50769384 26863196 MeRIP-seq:(Medium) rs1481119811 Functional Loss SNV dbSNP153 33..33 33 - - - 59496 RMVar_ID_59496 Human_SNP_ID_707266946 m1A Human chr22 + 50783595 50783595 50783595 CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCACGCCCGCCGGCCCAGCTCGCGCCGCAGCGCAC CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCGCGCCCGCCGGCCCAGCTCGCGCCGCAGCGCAC A G RPL23AP82 Ensembl:ENSG00000184319 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50783544..50783621;chr22:50783290..50783894 26863196 MeRIP-seq:(Medium) rs1434437075 Functional Loss SNV dbSNP153 33..33 33 - - - 59497 RMVar_ID_59497 Human_SNP_ID_707266947 m1A Human chr22 + 50783595 50783595 50783595 CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCACGCCCGCCGGCCCAGCTCGCGCCGCAGCGCAC CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCTCGCCCGCCGGCCCAGCTCGCGCCGCAGCGCAC A T RPL23AP82 Ensembl:ENSG00000184319 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50783544..50783621;chr22:50783290..50783894 26863196 MeRIP-seq:(Medium) rs1434437075 Functional Loss SNV dbSNP153 33..33 33 - - - 59498 RMVar_ID_59498 Human_SNP_ID_505802036 m1A Human chr12 - 70243316 70243316 70243316 AAGGTGGGAGCGACGACTGCAAAACGGCAGCGATGGGGTGGGTAGGCAGGCCGCTTTCAGCGCGC AAGGTGGGAGCGACGACTGCAAAACGGCAGCGGTGGGGTGGGTAGGCAGGCCGCTTTCAGCGCGC T C PRANCR Ensembl:ENSG00000257815 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:70242779..70243325 26863196 MeRIP-seq:(Medium) rs1376529138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1397461,Human_Splice_Rec_1397469,Human_Splice_Rec_1397483 59499 RMVar_ID_59499 Human_SNP_ID_505832052 m1A Human chr12 + 70366706 70366706 70366706 GCTCGGCGCCGGGGGCGGGAGGGGGCGGGGGGAGCACGCCAGCCGCCGAGAGTGGGGGGCGATGG GCTCGGCGCCGGGGGCGGGAGGGGGCGGGGGGGGCACGCCAGCCGCCGAGAGTGGGGGGCGATGG A G KCNMB4 Ensembl:ENSG00000135643 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:70366623..70366823 26863410 MeRIP-seq:(Medium) rs532514417 Functional Loss SNV dbSNP153 33..33 33 - - - 59500 RMVar_ID_59500 Human_SNP_ID_506131088 m1A Human chr12 + 71621730 71621730 71621730 TCTTCCCAACTTACCAGTTTTCTATTAATGACACTTTCCTTTTCCCAGTCTCAAAACCCTGAAAT TCTTCCCAACTTACCAGTTTTCTATTAATGACTCTTTCCTTTTCCCAGTCTCAAAACCCTGAAAT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:71621613..71621778 26863196 MeRIP-seq:(Medium) rs1021665755 Functional Loss SNV dbSNP153 33..33 33 - - - 59501 RMVar_ID_59501 Human_SNP_ID_506131175 m1A Human chr12 - 71622150 71622150 71622150 AGGACATTACTGTTAGGGGAGTTAAATAAACAAAAAGCAACAGGTAGAAGGGAATTTATGCAATG AGGACATTACTGTTAGGGGAGTTAAATAAACAGAAAGCAACAGGTAGAAGGGAATTTATGCAATG T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:71622108..71622198 26863196 MeRIP-seq:(Medium) rs1174755142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2352942,Human_RBP_ID_9701781,Human_RBP_ID_18633271,Human_RBP_ID_25002353 RMVar_hsa_circ_158266,RMVar_hsa_circ_158267,RMVar_hsa_circ_120461,RMVar_hsa_circ_50848,RMVar_hsa_circ_37631,RMVar_hsa_circ_53141,RMVar_hsa_circ_7401,RMVar_hsa_circ_107487,RMVar_hsa_circ_72760,RMVar_hsa_circ_54137,RMVar_hsa_circ_61495,RMVar_hsa_circ_158271,RMVar_hsa_circ_158269,RMVar_hsa_circ_357921,RMVar_hsa_circ_36545,RMVar_hsa_circ_680,RMVar_hsa_circ_10116 59502 RMVar_ID_59502 Human_SNP_ID_506136918 m1A Human chr12 - 71644272 71644272 71644272 AGGAAGCAGCAAACAAAGGCATGGAAGAAACTACAACAACAAAAAGAGCAGGAAAGACAGAAAGA AGGAAGCAGCAAACAAAGGCATGGAAGAAACTGCAACAACAAAAAGAGCAGGAAAGACAGAAAGA T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:71644151..71644886;chr12:71644128..71644925 26863196 MeRIP-seq:(Medium) rs764764444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872482,Human_RBP_ID_1479539,Human_RBP_ID_2353037,Human_RBP_ID_3941992,Human_RBP_ID_24543094,Human_RBP_ID_24551232,Human_RBP_ID_26323132,Human_RBP_ID_26911582,Human_RBP_ID_27805678 Human_Splice_Rec_1398920,Human_Splice_Rec_1398988 RMVar_hsa_circ_158266,RMVar_hsa_circ_31741,RMVar_hsa_circ_158276,RMVar_hsa_circ_67280,RMVar_hsa_circ_158284,RMVar_hsa_circ_353755,RMVar_hsa_circ_106049,RMVar_hsa_circ_158286,RMVar_hsa_circ_99513,RMVar_hsa_circ_158285,RMVar_hsa_circ_158287,RMVar_hsa_circ_158289,RMVar_hsa_circ_297434,RMVar_hsa_circ_327320,RMVar_hsa_circ_361343,RMVar_hsa_circ_158288,RMVar_hsa_circ_350236 59503 RMVar_ID_59503 Human_SNP_ID_506141688 m1A Human chr12 + 71663152 71663152 71663152 CCCACTCCTCGCCCCCGACTCCAGCGACTCCCACCCCGGTAAGGCCTGCCTCGAAAGCGGAAACG CCCACTCCTCGCCCCCGACTCCAGCGACTCCCCCCCCGGTAAGGCCTGCCTCGAAAGCGGAAACG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:71663105..71663183 26863196 MeRIP-seq:(Medium) rs535380093 Functional Loss SNV dbSNP153 33..33 33 - - - 59504 RMVar_ID_59504 Human_SNP_ID_506142199 m1A Human chr12 + 71664330 71664330 71664330 TCTAGTCGGCCATATTAATAAAGAGAAAGGGAAGGCTGACCGTCCTTCGCCTCCGCCCCCACATA TCTAGTCGGCCATATTAATAAAGAGAAAGGGAGGGCTGACCGTCCTTCGCCTCCGCCCCCACATA A G THAP2 Ensembl:ENSG00000173451 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:71664247..71664515 26863196 MeRIP-seq:(Medium) rs781466205 Functional Loss SNV dbSNP153 33..33 33 - - - 59505 RMVar_ID_59505 Human_SNP_ID_506163810 m1A Human chr12 - 71754951 71754951 71754951 CCTGGAAGGGCTGAGGGAAAGTCCGAGAATGAAGGGCCCCAGCCCACCACGTCAGGCACCGGAGG CCTGGAAGGGCTGAGGGAAAGTCCGAGAATGACGGGCCCCAGCCCACCACGTCAGGCACCGGAGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:71754901..71755225 26863196 MeRIP-seq:(Medium) rs555071396 Functional Loss SNV dbSNP153 33..33 33 - - - 59506 RMVar_ID_59506 Human_SNP_ID_506163866 m1A Human chr12 + 71755125 71755125 71755125 CGCGACACTCGGGCTCGGGCGGCCGGGAAGCGACGGGATGGCTGCGGCCGGCGGCGGCGGCGGCG CGCGACACTCGGGCTCGGGCGGCCGGGAAGCGGCGGGATGGCTGCGGCCGGCGGCGGCGGCGGCG A G RAB21 Ensembl:ENSG00000080371 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:71754876..71755300 26863196 MeRIP-seq:(Medium) rs1387011898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810167,Human_RBP_ID_6219484,Human_RBP_ID_9322627,Human_RBP_ID_9352764,Human_RBP_ID_17826619,Human_RBP_ID_22436641 59507 RMVar_ID_59507 Human_SNP_ID_506167771 m1A Human chr12 + 71770551 71770551 71770551 AAAGTTCACCATAGTTGCAATCGCAGATTTGTATTTTTCTTCTGATCTAATAAGCATTTGTTGCT AAAGTTCACCATAGTTGCAATCGCAGATTTGTGTTTTTCTTCTGATCTAATAAGCATTTGTTGCT A G RAB21 Ensembl:ENSG00000080371 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:71770549..71770618 26863196 MeRIP-seq:(Medium) rs757505083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273943,RMVar_hsa_circ_309111,RMVar_hsa_circ_158297 59508 RMVar_ID_59508 Human_SNP_ID_506184870 m1A Human chr12 + 71839809 71839809 71839809 GAAACATGGCGGCGGCGGGTGTTGTGAGCGGGAAGGTAGGTAACGGCCTCCAGGAAGACCTCGGC GAAACATGGCGGCGGCGGGTGTTGTGAGCGGGCAGGTAGGTAACGGCCTCCAGGAAGACCTCGGC A C TBC1D15 Ensembl:ENSG00000121749 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h chr12:71839789..71839864;chr12:71839775..71839919;chr12:71839776..71839892;chr12:71839776..71839886 26863196,26863410,26863196 MeRIP-seq:(Medium) rs75347629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417663,Human_RBP_ID_19056639,Human_RBP_ID_26321731,Human_RBP_ID_27805685 Human_Splice_Rec_1399175,Human_Splice_Rec_1399187,Human_Splice_Rec_1399221,Human_Splice_Rec_1399233,Human_Splice_Rec_1399243,Human_Splice_Rec_1399255,Human_Splice_Rec_1399265,Human_Splice_Rec_1399285,Human_Splice_Rec_1399319,Human_Splice_Rec_1399349,Human_Splice_Rec_1399381,Human_Splice_Rec_1399389 59509 RMVar_ID_59509 Human_SNP_ID_506184871 m1A Human chr12 + 71839809 71839809 71839809 GAAACATGGCGGCGGCGGGTGTTGTGAGCGGGAAGGTAGGTAACGGCCTCCAGGAAGACCTCGGC GAAACATGGCGGCGGCGGGTGTTGTGAGCGGGGAGGTAGGTAACGGCCTCCAGGAAGACCTCGGC A G TBC1D15 Ensembl:ENSG00000121749 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h chr12:71839789..71839864;chr12:71839775..71839919;chr12:71839776..71839892;chr12:71839776..71839886 26863196,26863410,26863196 MeRIP-seq:(Medium) rs75347629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417663,Human_RBP_ID_19056639,Human_RBP_ID_26321731,Human_RBP_ID_27805685 Human_Splice_Rec_1399175,Human_Splice_Rec_1399187,Human_Splice_Rec_1399221,Human_Splice_Rec_1399233,Human_Splice_Rec_1399243,Human_Splice_Rec_1399255,Human_Splice_Rec_1399265,Human_Splice_Rec_1399285,Human_Splice_Rec_1399319,Human_Splice_Rec_1399349,Human_Splice_Rec_1399381,Human_Splice_Rec_1399389 59510 RMVar_ID_59510 Human_SNP_ID_506185240 m1A Human chr12 - 71841115 71841115 71841115 ATAATCTTCAAATACGCAGTAAGTCAAGCAGTATATCAGCATCCACCCTGAATATAAAAAGAAAA ATAATCTTCAAATACGCAGTAAGTCAAGCAGTGTATCAGCATCCACCCTGAATATAAAAAGAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:71841113..71841197 26863196 MeRIP-seq:(Medium) rs996566971 Functional Loss SNV dbSNP153 33..33 33 - - - 59511 RMVar_ID_59511 Human_SNP_ID_506192817 m1A Human chr12 + 71872054 71872054 71872054 TAGTACTCAATAGAAATTATGTGACTAACTTTATTTTTGCTGTTTTAGATTATATATGAACAAGA TAGTACTCAATAGAAATTATGTGACTAACTTTGTTTTTGCTGTTTTAGATTATATATGAACAAGA A G TBC1D15 Ensembl:ENSG00000121749 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:71872051..71872175 26863196 MeRIP-seq:(Medium) rs751629838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71433,RMVar_hsa_circ_347907 59512 RMVar_ID_59512 Human_SNP_ID_506205280 m1A Human chr12 + 71923099 71923099 71923099 AATGTTGTCATGACTCCTTGTCCTACATCTGCATTTCAAAGTAATGCCTTGCCTACACTCTCTGC AATGTTGTCATGACTCCTTGTCCTACATCTGCGTTTCAAAGTAATGCCTTGCCTACACTCTCTGC A G TBC1D15 Ensembl:ENSG00000121749 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:71923048..71923134 26863196 MeRIP-seq:(Medium) rs1314125245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8069530 59513 RMVar_ID_59513 Human_SNP_ID_506853541 m1A Human chr12 - 74538769 74538769 74538769 ACGTCCAAACTGTCCAAGAAGCCCTTGACATCAGGCAGACAGAAAGGCTGAGGAACCAAAAATTT ACGTCCAAACTGTCCAAGAAGCCCTTGACATCGGGCAGACAGAAAGGCTGAGGAACCAAAAATTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:74538720..74538821 32194978 MeRIP-seq:(Medium) rs955334440 Functional Loss SNV dbSNP153 33..33 33 - - - 59514 RMVar_ID_59514 Human_SNP_ID_506854202 m1A Human chr12 - 74541035 74541035 74541035 TGCTATTAAAAGGAAGGTAGGTAGGGAAAGGGAGAGTTCCTAACCACTGTCAACTATATGGTAGG TGCTATTAAAAGGAAGGTAGGTAGGGAAAGGGGGAGTTCCTAACCACTGTCAACTATATGGTAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:74540808..74541156 32194978 MeRIP-seq:(Medium) rs1049224097 Functional Loss SNV dbSNP153 33..33 33 - - - 59515 RMVar_ID_59515 Human_SNP_ID_506964640 m1A Human chr12 - 74953573 74953573 74953573 GAGCCACTGCAGGCGCAGATCTTGGTGGTAGTAGCAAATATTAAAACAACAATAAAAAAATTAGG GAGCCACTGCAGGCGCAGATCTTGGTGGTAGTTGCAAATATTAAAACAACAATAAAAAAATTAGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:74953551..74953625 26863196 MeRIP-seq:(Medium) rs1367876687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275635,Human_RBP_ID_994534,Human_RBP_ID_1127515,Human_RBP_ID_1168870,Human_RBP_ID_1477841,Human_RBP_ID_1801538,Human_RBP_ID_5417331,Human_RBP_ID_5438053,Human_RBP_ID_5462148,Human_RBP_ID_5492089,Human_RBP_ID_6221114,Human_RBP_ID_8069547,Human_RBP_ID_8247861,Human_RBP_ID_8383802,Human_RBP_ID_8785421,Human_RBP_ID_9021215,Human_RBP_ID_12033335,Human_RBP_ID_16993710,Human_RBP_ID_17240665,Human_RBP_ID_17356179,Human_RBP_ID_17473679,Human_RBP_ID_17685357,Human_RBP_ID_17826891,Human_RBP_ID_18206653,Human_RBP_ID_18264168,Human_RBP_ID_18434782,Human_RBP_ID_18511360,Human_RBP_ID_19030503,Human_RBP_ID_21918360,Human_RBP_ID_22001522,Human_RBP_ID_22177604,Human_RBP_ID_22421132,Human_RBP_ID_22795720,Human_RBP_ID_23270160,Human_RBP_ID_26615214,Human_RBP_ID_26748112,Human_RBP_ID_26911751,Human_RBP_ID_27155014,Human_RBP_ID_27218520,Human_RBP_ID_27425182,Human_RBP_ID_27633483 59516 RMVar_ID_59516 Human_SNP_ID_507050374 m1A Human chr12 - 75282557 75282557 75282557 CATGGCGAAACCCCGCCTCTACTAAAAATACAAAAAATAGCTAGGTGTGGTGGCGGGCGCCTGTA CATGGCGAAACCCCGCCTCTACTAAAAATACACAAAATAGCTAGGTGTGGTGGCGGGCGCCTGTA T G CAPS2 Ensembl:ENSG00000180881 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:75282534..75282618 26863410 MeRIP-seq:(Medium) rs1409246502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158339,RMVar_hsa_circ_278167,RMVar_hsa_circ_336100,RMVar_hsa_circ_344184,RMVar_hsa_circ_310900,RMVar_hsa_circ_158340,RMVar_hsa_circ_158338 59517 RMVar_ID_59517 Human_SNP_ID_507231022 m1A Human chr12 - 76030614 76030603 76030615 CCACACCCTCACCCGCACCCGCATCCGCACCAAATACCGCACCCACACCCACAGCCGCACTCGCA CCACACCCTCACCCGCACCCGCATCCGCACC____________CACACCCACAGCCGCACTCGCA GGGTGCGGTATTT G PHLDA1 Ensembl:ENSG00000139289 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76030566..76030878 26863196 MeRIP-seq:(Medium) rs1489794988 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_114158,Human_RBP_ID_194809,Human_RBP_ID_753777,Human_RBP_ID_811397,Human_RBP_ID_1065484,Human_RBP_ID_17474839,Human_RBP_ID_18934646,Human_RBP_ID_22383712,Human_RBP_ID_24529918 RMVar_hsa_circ_123121,RMVar_hsa_circ_158349 59518 RMVar_ID_59518 Human_SNP_ID_507237801 m1A Human chr12 - 76056120 76056120 76056120 AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAAGATGAAGAAAAAGAAGACCCCAAAGGAATTCC AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAGGATGAAGAAAAAGAAGACCCCAAAGGAATTCC T C NAP1L1 Ensembl:ENSG00000187109 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1059143 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_194442,Human_RBP_ID_811191,Human_RBP_ID_877958,Human_RBP_ID_1477980,Human_RBP_ID_1801678,Human_RBP_ID_2368915,Human_RBP_ID_4241894,Human_RBP_ID_6222062,Human_RBP_ID_8247862,Human_RBP_ID_8383957,Human_RBP_ID_9365251,Human_RBP_ID_17240742,Human_RBP_ID_17473808,Human_RBP_ID_18410892,Human_RBP_ID_18526788,Human_RBP_ID_18633610,Human_RBP_ID_22001529,Human_RBP_ID_22909227,Human_RBP_ID_23113344,Human_RBP_ID_23574917,Human_RBP_ID_24543107,Human_RBP_ID_25003582,Human_RBP_ID_26320975,Human_RBP_ID_26911848,Human_RBP_ID_27805738 Human_Splice_Rec_1400534,Human_Splice_Rec_1400535,Human_Splice_Rec_1400562,Human_Splice_Rec_1400563,Human_Splice_Rec_1400588,Human_Splice_Rec_1400589,Human_Splice_Rec_1400618,Human_Splice_Rec_1400619,Human_Splice_Rec_1400644,Human_Splice_Rec_1400645,Human_Splice_Rec_1400666,Human_Splice_Rec_1400667,Human_Splice_Rec_1400690,Human_Splice_Rec_1400691,Human_Splice_Rec_1400716,Human_Splice_Rec_1400717,Human_Splice_Rec_1400742,Human_Splice_Rec_1400743,Human_Splice_Rec_1400770,Human_Splice_Rec_1400771,Human_Splice_Rec_1400796,Human_Splice_Rec_1400797,Human_Splice_Rec_1400809,Human_Splice_Rec_1400840,Human_Splice_Rec_1400841,Human_Splice_Rec_1400858,Human_Splice_Rec_1400859,Human_Splice_Rec_1400878,Human_Splice_Rec_1400879,Human_Splice_Rec_1400900,Human_Splice_Rec_1400901,Human_Splice_Rec_1400918,Human_Splice_Rec_1400919,Human_Splice_Rec_1400932,Human_Splice_Rec_1400933,Human_Splice_Rec_1400948,Human_Splice_Rec_1400949,Human_Splice_Rec_1400962,Human_Splice_Rec_1400963,Human_Splice_Rec_1400970 Human_miRNA_ID_2157685,Human_miRNA_ID_2157686 GWAS_ID_6929,GWAS_ID_6930 RMVar_hsa_circ_1721,RMVar_hsa_circ_84271,RMVar_hsa_circ_158351,RMVar_hsa_circ_125050,RMVar_hsa_circ_352895,RMVar_hsa_circ_339462,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158355,RMVar_hsa_circ_158356,RMVar_hsa_circ_83129,RMVar_hsa_circ_41971,RMVar_hsa_circ_158358,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_40655,RMVar_hsa_circ_158361,RMVar_hsa_circ_303154,RMVar_hsa_circ_309215,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_367606 59519 RMVar_ID_59519 Human_SNP_ID_507237802 m1A Human chr12 - 76056120 76056120 76056120 AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAAGATGAAGAAAAAGAAGACCCCAAAGGAATTCC AAAGAAAAGGCCAAGATTGAAGATGAGAAAAACGATGAAGAAAAAGAAGACCCCAAAGGAATTCC T G NAP1L1 Ensembl:ENSG00000187109 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1059143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194442,Human_RBP_ID_811191,Human_RBP_ID_877958,Human_RBP_ID_1477980,Human_RBP_ID_1801678,Human_RBP_ID_2368915,Human_RBP_ID_4241894,Human_RBP_ID_6222062,Human_RBP_ID_8247862,Human_RBP_ID_8383957,Human_RBP_ID_9365251,Human_RBP_ID_17240742,Human_RBP_ID_17473808,Human_RBP_ID_18410892,Human_RBP_ID_18526788,Human_RBP_ID_18633610,Human_RBP_ID_22001529,Human_RBP_ID_22909227,Human_RBP_ID_23113344,Human_RBP_ID_23574917,Human_RBP_ID_24543107,Human_RBP_ID_25003582,Human_RBP_ID_26320975,Human_RBP_ID_26911848,Human_RBP_ID_27805738 Human_Splice_Rec_1400534,Human_Splice_Rec_1400535,Human_Splice_Rec_1400562,Human_Splice_Rec_1400563,Human_Splice_Rec_1400588,Human_Splice_Rec_1400589,Human_Splice_Rec_1400618,Human_Splice_Rec_1400619,Human_Splice_Rec_1400644,Human_Splice_Rec_1400645,Human_Splice_Rec_1400666,Human_Splice_Rec_1400667,Human_Splice_Rec_1400690,Human_Splice_Rec_1400691,Human_Splice_Rec_1400716,Human_Splice_Rec_1400717,Human_Splice_Rec_1400742,Human_Splice_Rec_1400743,Human_Splice_Rec_1400770,Human_Splice_Rec_1400771,Human_Splice_Rec_1400796,Human_Splice_Rec_1400797,Human_Splice_Rec_1400809,Human_Splice_Rec_1400840,Human_Splice_Rec_1400841,Human_Splice_Rec_1400858,Human_Splice_Rec_1400859,Human_Splice_Rec_1400878,Human_Splice_Rec_1400879,Human_Splice_Rec_1400900,Human_Splice_Rec_1400901,Human_Splice_Rec_1400918,Human_Splice_Rec_1400919,Human_Splice_Rec_1400932,Human_Splice_Rec_1400933,Human_Splice_Rec_1400948,Human_Splice_Rec_1400949,Human_Splice_Rec_1400962,Human_Splice_Rec_1400963,Human_Splice_Rec_1400970 Human_miRNA_ID_2157685,Human_miRNA_ID_2157686 GWAS_ID_6929,GWAS_ID_6930 RMVar_hsa_circ_1721,RMVar_hsa_circ_84271,RMVar_hsa_circ_158351,RMVar_hsa_circ_125050,RMVar_hsa_circ_352895,RMVar_hsa_circ_339462,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158355,RMVar_hsa_circ_158356,RMVar_hsa_circ_83129,RMVar_hsa_circ_41971,RMVar_hsa_circ_158358,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_40655,RMVar_hsa_circ_158361,RMVar_hsa_circ_303154,RMVar_hsa_circ_309215,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_367606 59520 RMVar_ID_59520 Human_SNP_ID_507240825 m1A Human chr12 - 76067472 76067472 76067472 TCCTTCTTTCGATGCCCTTTTTTTTTTAAAGCACGTCAGCTAACTGTTCAGATGATGCAAAATCC TCCTTCTTTCGATGCCCTTTTTTTTTTAAAGCGCGTCAGCTAACTGTTCAGATGATGCAAAATCC T C NAP1L1 Ensembl:ENSG00000187109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:76067451..76067475 26863196 MeRIP-seq:(Medium) rs201324738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877961,Human_RBP_ID_1801727,Human_RBP_ID_4241907,Human_RBP_ID_12035686,Human_RBP_ID_22177670 Human_Splice_Rec_1400528,Human_Splice_Rec_1400556,Human_Splice_Rec_1400582,Human_Splice_Rec_1400612,Human_Splice_Rec_1400640,Human_Splice_Rec_1400736,Human_Splice_Rec_1400764,Human_Splice_Rec_1400790,Human_Splice_Rec_1400832,Human_Splice_Rec_1400872,Human_Splice_Rec_1400896,Human_Splice_Rec_1400912,Human_Splice_Rec_1400926,Human_Splice_Rec_1400942,Human_Splice_Rec_1400956,Human_Splice_Rec_1400980 RMVar_hsa_circ_352895,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158356,RMVar_hsa_circ_158357,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_158363,RMVar_hsa_circ_286148,RMVar_hsa_circ_323096,RMVar_hsa_circ_268347,RMVar_hsa_circ_311674,RMVar_hsa_circ_286605,RMVar_hsa_circ_158364 59521 RMVar_ID_59521 Human_SNP_ID_507241240 m1A Human chr12 - 76068832 76068830 76068832 GTCTACTAGAGGGTAGTTATAAGTACCAGTCTATTTTTTTGGACCCTTGCTCATTGTCCCATTTA GTCTACTAGAGGGTAGTTATAAGTACCAGTCT__TTTTTTGGACCCTTGCTCATTGTCCCATTTA AAT A NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1215611182 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9702667,Human_RBP_ID_22177674,Human_RBP_ID_22354025,Human_RBP_ID_24407688,Human_RBP_ID_24467852 RMVar_hsa_circ_352895,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158356,RMVar_hsa_circ_158357,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_158363,RMVar_hsa_circ_286148,RMVar_hsa_circ_323096,RMVar_hsa_circ_268347,RMVar_hsa_circ_311674,RMVar_hsa_circ_286605,RMVar_hsa_circ_158364 59522 RMVar_ID_59522 Human_SNP_ID_507241241 m1A Human chr12 - 76068832 76068832 76068832 GTCTACTAGAGGGTAGTTATAAGTACCAGTCTATTTTTTTGGACCCTTGCTCATTGTCCCATTTA GTCTACTAGAGGGTAGTTATAAGTACCAGTCTTTTTTTTTGGACCCTTGCTCATTGTCCCATTTA T A NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10880034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9702667,Human_RBP_ID_22177674,Human_RBP_ID_22354025,Human_RBP_ID_24407688,Human_RBP_ID_24467852 GWAS_ID_6931,GWAS_ID_6932,GWAS_ID_6933,GWAS_ID_6934,GWAS_ID_6935,GWAS_ID_6936,GWAS_ID_6937,GWAS_ID_6938 RMVar_hsa_circ_352895,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158356,RMVar_hsa_circ_158357,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_158363,RMVar_hsa_circ_286148,RMVar_hsa_circ_323096,RMVar_hsa_circ_268347,RMVar_hsa_circ_311674,RMVar_hsa_circ_286605,RMVar_hsa_circ_158364 59523 RMVar_ID_59523 Human_SNP_ID_507241242 m1A Human chr12 - 76068832 76068832 76068832 GTCTACTAGAGGGTAGTTATAAGTACCAGTCTATTTTTTTGGACCCTTGCTCATTGTCCCATTTA GTCTACTAGAGGGTAGTTATAAGTACCAGTCTGTTTTTTTGGACCCTTGCTCATTGTCCCATTTA T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10880034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9702667,Human_RBP_ID_22177674,Human_RBP_ID_22354025,Human_RBP_ID_24407688,Human_RBP_ID_24467852 GWAS_ID_6931,GWAS_ID_6932,GWAS_ID_6933,GWAS_ID_6934,GWAS_ID_6935,GWAS_ID_6936,GWAS_ID_6937,GWAS_ID_6938 RMVar_hsa_circ_352895,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158356,RMVar_hsa_circ_158357,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_158363,RMVar_hsa_circ_286148,RMVar_hsa_circ_323096,RMVar_hsa_circ_268347,RMVar_hsa_circ_311674,RMVar_hsa_circ_286605,RMVar_hsa_circ_158364 59524 RMVar_ID_59524 Human_SNP_ID_507245224 m1A Human chr12 + 76084111 76084111 76084111 ATTCGCAGCCTCCGCCGTTCTTTTCATCTCCCAGCGGCCTCCCTCCTGGTATTATTTTTGAGGGA ATTCGCAGCCTCCGCCGTTCTTTTCATCTCCCGGCGGCCTCCCTCCTGGTATTATTTTTGAGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76084108..76084265 26863196 MeRIP-seq:(Medium) rs1273058806 Functional Loss SNV dbSNP153 33..33 33 - - - 59525 RMVar_ID_59525 Human_SNP_ID_507245425 m1A Human chr12 + 76084650 76084650 76084650 AGGGCGGCAGCGGCAGCAGCAGCGGGAGGAGCAGGAGGCGGCGCCGCGAGCAGATGGCGCTAAAA AGGGCGGCAGCGGCAGCAGCAGCGGGAGGAGCTGGAGGCGGCGCCGCGAGCAGATGGCGCTAAAA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:76084551..76084675 26863196 MeRIP-seq:(Medium) rs1343309710 Functional Loss SNV dbSNP153 33..33 33 - - - 59526 RMVar_ID_59526 Human_SNP_ID_507313220 m1A Human chr12 - 76348362 76348362 76348362 TCTGCAAGCTGGTCAAAAAGGGGAAGCGGCCCAGATATGTTAAGTTCTATGGCCGCTGCAGGGTC TCTGCAAGCTGGTCAAAAAGGGGAAGCGGCCCGGATATGTTAAGTTCTATGGCCGCTGCAGGGTC T C BBS10 Ensembl:ENSG00000179941 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76348202..76348392 26863196 MeRIP-seq:(Medium) rs886049853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_994652 Clinvar_Rec_198 59527 RMVar_ID_59527 Human_SNP_ID_507332506 m1A Human chr12 - 76430026 76430026 76430026 CATGGCTGTTTGAGGAGCTGTAGTTGTGTTGGAAGTCAGCAGGCCTGTTACCAGGGGTGCTAGTG CATGGCTGTTTGAGGAGCTGTAGTTGTGTTGGGAGTCAGCAGGCCTGTTACCAGGGGTGCTAGTG T C OSBPL8 Ensembl:ENSG00000091039 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76430023..76430132 26863196 MeRIP-seq:(Medium) rs1425526050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810572,Human_RBP_ID_17113289 RMVar_hsa_circ_112449,RMVar_hsa_circ_158368,RMVar_hsa_circ_158370,RMVar_hsa_circ_88905,RMVar_hsa_circ_120942,RMVar_hsa_circ_26544,RMVar_hsa_circ_158376,RMVar_hsa_circ_158374,RMVar_hsa_circ_11867,RMVar_hsa_circ_6120,RMVar_hsa_circ_18796,RMVar_hsa_circ_44360,RMVar_hsa_circ_20034 59528 RMVar_ID_59528 Human_SNP_ID_507363743 m1A Human chr12 - 76559609 76559609 76559609 GTCCGCCCGGGCTGGTGGACCTCGGGGCCGAAAGTTCCCGCCCCGCTCGGGGGCTGAGCCGGCAG GTCCGCCCGGGCTGGTGGACCTCGGGGCCGAAGGTTCCCGCCCCGCTCGGGGGCTGAGCCGGCAG T C OSBPL8 Ensembl:ENSG00000091039 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:76559568..76559687 26863196 MeRIP-seq:(Medium) rs180921741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246220,Human_RBP_ID_5462333,Human_RBP_ID_8787335,Human_RBP_ID_18417487,Human_RBP_ID_18434788,Human_RBP_ID_22040041 59529 RMVar_ID_59529 Human_SNP_ID_507363763 m1A Human chr12 - 76559667 76559667 76559667 TAGCTTTGGACGCCGCAGTAGCCGCTGCCGGTAGCAAGCCGACTGAGGGAAGGTGGGGGTCCGCC TAGCTTTGGACGCCGCAGTAGCCGCTGCCGGTGGCAAGCCGACTGAGGGAAGGTGGGGGTCCGCC T C OSBPL8 Ensembl:ENSG00000091039 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76559616..76559731 26863196 MeRIP-seq:(Medium) rs747829866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246221,Human_RBP_ID_5462333,Human_RBP_ID_8787335,Human_RBP_ID_9279153,Human_RBP_ID_9322632,Human_RBP_ID_9366689,Human_RBP_ID_18417665,Human_RBP_ID_22039467 59530 RMVar_ID_59530 Human_SNP_ID_507412760 m1A Human chr12 - 76763885 76763885 76763885 CCGGGCGGTTGAGACAGTCGCTTGGGAAACCTAGCAGCTGCTCAGGAGCGAGAACAGAGCTCCGG CCGGGCGGTTGAGACAGTCGCTTGGGAAACCTTGCAGCTGCTCAGGAGCGAGAACAGAGCTCCGG T A lnc-CSRP2-2 RNACentral:URS0000D5BB75 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76763806..76763918 26863196 MeRIP-seq:(Medium) rs1412766084 Functional Loss SNV dbSNP153 33..33 33 - - - 59531 RMVar_ID_59531 Human_SNP_ID_507413013 m1A Human chr12 + 76764299 76764299 76764299 ATGGCGGACGGCCCGGATGAGTACGATACCGAAGCGGGCTGTGTGCCCCTTCTCCACCCAGAGGT ATGGCGGACGGCCCGGATGAGTACGATACCGAGGCGGGCTGTGTGCCCCTTCTCCACCCAGAGGT A G ZDHHC17 Ensembl:ENSG00000186908 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:76764128..76764576;chr12:76764124..76764427 26863196 MeRIP-seq:(Medium) rs756110340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755299,Human_RBP_ID_3943335,Human_RBP_ID_4260087,Human_RBP_ID_9365263,Human_RBP_ID_17830468 Human_Splice_Rec_1401355,Human_Splice_Rec_1401385,Human_Splice_Rec_1401401,Human_Splice_Rec_1401417,Human_Splice_Rec_1401427,Human_Splice_Rec_1401437,Human_Splice_Rec_1401447,Human_Splice_Rec_1401451 59532 RMVar_ID_59532 Human_SNP_ID_507413021 m1A Human chr12 - 76764308 76764308 76764308 CGGTTCCTCACCTCTGGGTGGAGAAGGGGCACACAGCCCGCTTCGGTATCGTACTCATCCGGGCC CGGTTCCTCACCTCTGGGTGGAGAAGGGGCACGCAGCCCGCTTCGGTATCGTACTCATCCGGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76764135..76764495 26863196 MeRIP-seq:(Medium) rs754044344 Functional Loss SNV dbSNP153 33..33 33 - - - 59533 RMVar_ID_59533 Human_SNP_ID_507441425 m1A Human chr12 - 76878960 76878960 76878960 TCCAGCCCAGCCTCGCTAGCTCCGCCTGCGGTACGTGCTCCCGCCTCCGACTCAAGTGAGTAGGG TCCAGCCCAGCCTCGCTAGCTCCGCCTGCGGTGCGTGCTCCCGCCTCCGACTCAAGTGAGTAGGG T C CSRP2 Ensembl:ENSG00000175183 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:76878926..76879025 26863196 MeRIP-seq:(Medium) rs963191538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230111,Human_RBP_ID_4242158 Human_Splice_Rec_1401519,Human_Splice_Rec_1401533,Human_Splice_Rec_1401555,Human_Splice_Rec_1401565 59534 RMVar_ID_59534 Human_SNP_ID_507441439 m1A Human chr12 - 76878984 76878984 76878984 ATCTCGGACTCCCTGGACCCTCCCTCCAGCCCAGCCTCGCTAGCTCCGCCTGCGGTACGTGCTCC ATCTCGGACTCCCTGGACCCTCCCTCCAGCCCGGCCTCGCTAGCTCCGCCTGCGGTACGTGCTCC T C CSRP2 Ensembl:ENSG00000175183 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:76878852..76878988 26863196 MeRIP-seq:(Medium) rs983261154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230111,Human_RBP_ID_4242160 Human_Splice_Rec_1401519,Human_Splice_Rec_1401533,Human_Splice_Rec_1401545,Human_Splice_Rec_1401555,Human_Splice_Rec_1401563,Human_Splice_Rec_1401565 Human_miRNA_ID_1157047,Human_miRNA_ID_1364235,Human_miRNA_ID_1394456 59535 RMVar_ID_59535 Human_SNP_ID_507441440 m1A Human chr12 - 76878984 76878984 76878984 ATCTCGGACTCCCTGGACCCTCCCTCCAGCCCAGCCTCGCTAGCTCCGCCTGCGGTACGTGCTCC ATCTCGGACTCCCTGGACCCTCCCTCCAGCCCCGCCTCGCTAGCTCCGCCTGCGGTACGTGCTCC T G CSRP2 Ensembl:ENSG00000175183 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:76878852..76878988 26863196 MeRIP-seq:(Medium) rs983261154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230111,Human_RBP_ID_4242160 Human_Splice_Rec_1401519,Human_Splice_Rec_1401533,Human_Splice_Rec_1401545,Human_Splice_Rec_1401555,Human_Splice_Rec_1401563,Human_Splice_Rec_1401565 Human_miRNA_ID_1157047,Human_miRNA_ID_1364235,Human_miRNA_ID_1394456 59536 RMVar_ID_59536 Human_SNP_ID_507441445 m1A Human chr12 - 76878989 76878989 76878989 CTGGGATCTCGGACTCCCTGGACCCTCCCTCCAGCCCAGCCTCGCTAGCTCCGCCTGCGGTACGT CTGGGATCTCGGACTCCCTGGACCCTCCCTCCGGCCCAGCCTCGCTAGCTCCGCCTGCGGTACGT T C CSRP2 Ensembl:ENSG00000175183 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:76878871..76879000 26863196 MeRIP-seq:(Medium) rs1311038661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230111,Human_RBP_ID_4242160 Human_Splice_Rec_1401519,Human_Splice_Rec_1401533,Human_Splice_Rec_1401545,Human_Splice_Rec_1401555,Human_Splice_Rec_1401563,Human_Splice_Rec_1401565 Human_miRNA_ID_1157047,Human_miRNA_ID_1364235,Human_miRNA_ID_1394456 59537 RMVar_ID_59537 Human_SNP_ID_507441612 m1A Human chr12 - 76879430 76879430 76879430 GCTGACTTTCTACTGCTGGAGCCTCCCGGCCCATGACTGTCTCCGCGAAGAGGGGGATCGGCGCT GCTGACTTTCTACTGCTGGAGCCTCCCGGCCCGTGACTGTCTCCGCGAAGAGGGGGATCGGCGCT T C lnc-CSRP2-1 RNACentral:URS00008B5D74 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:76879379..76879537 26863196 MeRIP-seq:(Medium) rs1587110 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6939,GWAS_ID_6940 59538 RMVar_ID_59538 Human_SNP_ID_507476528 m1A Human chr12 - 77030023 77030023 77030023 CTGTTCATGCTGTATGGAAGTCTGCAGGAGGGACCAGCGTCAGGGTCAGGGTCAGAGAGGGATGA CTGTTCATGCTGTATGGAAGTCTGCAGGAGGGGCCAGCGTCAGGGTCAGGGTCAGAGAGGGATGA T C E2F7 Ensembl:ENSG00000165891 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:77029882..77030032 32194978 MeRIP-seq:(Medium) rs1327748246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6224197,Human_RBP_ID_8785666 RMVar_hsa_circ_42406,RMVar_hsa_circ_63774,RMVar_hsa_circ_370131,RMVar_hsa_circ_158395 59539 RMVar_ID_59539 Human_SNP_ID_507482355 m1A Human chr12 + 77056064 77056064 77056064 TCTTTCTGGAGTAAATTTTTTTTGCTTCGATAAATCAATTGGTTCATTTTTTATTGGAGTCTTCG TCTTTCTGGAGTAAATTTTTTTTGCTTCGATATATCAATTGGTTCATTTTTTATTGGAGTCTTCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:77055961..77056104 26863196 MeRIP-seq:(Medium) rs757642250 Functional Loss SNV dbSNP153 33..33 33 - - - 59540 RMVar_ID_59540 Human_SNP_ID_507483649 m1A Human chr12 - 77061898 77061898 77061898 TTTGGGCTAAGCCTTAGTGGATGAGGAAGCTCAACCTACAAGAAAGCAAGAGTGAACGAGATGGA TTTGGGCTAAGCCTTAGTGGATGAGGAAGCTCGACCTACAAGAAAGCAAGAGTGAACGAGATGGA T C E2F7 Ensembl:ENSG00000165891 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:77061896..77062028 26863196 MeRIP-seq:(Medium) rs1478794371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19527 59541 RMVar_ID_59541 Human_SNP_ID_507484469 m1A Human chr12 - 77065489 77065489 77065489 CTGCCCGGACGCCGCGGGGTCCCCGCCAGCCCAGGGCACTCGGCGCGGGGATCTGCGCGCCTCGC CTGCCCGGACGCCGCGGGGTCCCCGCCAGCCCGGGGCACTCGGCGCGGGGATCTGCGCGCCTCGC T C E2F7 Ensembl:ENSG00000165891 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:77065438..77065526 26863196 MeRIP-seq:(Medium) rs1041755552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4242295 59542 RMVar_ID_59542 Human_SNP_ID_508090361 m1A Human chr12 - 79534361 79534361 79534361 TGGGCAGGATTTTTGATAGGTGGAGGGAATGCAAAGTGTTACGGTCGAGGGGAACTTCATGGATG TGGGCAGGATTTTTGATAGGTGGAGGGAATGCGAAGTGTTACGGTCGAGGGGAACTTCATGGATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79534319..79534450 26863196 MeRIP-seq:(Medium) rs1329981180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2357630 59543 RMVar_ID_59543 Human_SNP_ID_508092678 m1A Human chr12 - 79543678 79543678 79543678 AGTCCGGGCCAGGAACAATGGTAATTGTGGGAAACTCAACAAAGAGTGAGTACAGCTGAAGGAGC AGTCCGGGCCAGGAACAATGGTAATTGTGGGAGACTCAACAAAGAGTGAGTACAGCTGAAGGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79543630..79543695 26863196 MeRIP-seq:(Medium) rs1170974760 Functional Loss SNV dbSNP153 33..33 33 - - - 59544 RMVar_ID_59544 Human_SNP_ID_508107915 m1A Human chr12 - 79604635 79604635 79604635 TGGAGGGTGAAGAGAATGGGGCAGTGAAAGATACTAAAAGGATGGAAGCCAGTTAAGTAGTTGTT TGGAGGGTGAAGAGAATGGGGCAGTGAAAGATGCTAAAAGGATGGAAGCCAGTTAAGTAGTTGTT T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:79604633..79604730 26863196 MeRIP-seq:(Medium) rs1323337020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9716558 Human_Splice_Rec_1402332 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 59545 RMVar_ID_59545 Human_SNP_ID_508107925 m1A Human chr12 + 79604667 79604667 79604667 TATCTTTCACTGCCCCATTCTCTTCACCCTCCAACACTCCCACTCCTCGTAACAGCTCCTTGCTC TATCTTTCACTGCCCCATTCTCTTCACCCTCCGACACTCCCACTCCTCGTAACAGCTCCTTGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79604626..79604746 26863196 MeRIP-seq:(Medium) rs1299398977 Functional Loss SNV dbSNP153 33..33 33 - - - 59546 RMVar_ID_59546 Human_SNP_ID_508116368 m1A Human chr12 - 79637372 79637372 79637372 ATGGTAGATGAAAAGGGTATTACCAGAGAAGGAGGCGGATTAAAGAAGTGGCATTACTGATAGGA ATGGTAGATGAAAAGGGTATTACCAGAGAAGGCGGCGGATTAAAGAAGTGGCATTACTGATAGGA T G PAWR Ensembl:ENSG00000177425 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:79637367..79637459 26863196 MeRIP-seq:(Medium) rs1357663695 Functional Loss SNV dbSNP153 33..33 33 - - - 59547 RMVar_ID_59547 Human_SNP_ID_508125263 m1A Human chr12 - 79672099 79672099 79672099 CAGGTGGGAGGTAGGGGCCATGGAGAGACGGGATTGCGTATGGAATATGTTTTAGAGGTAGAGCT CAGGTGGGAGGTAGGGGCCATGGAGAGACGGGGTTGCGTATGGAATATGTTTTAGAGGTAGAGCT T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79672098..79672209 26863196 MeRIP-seq:(Medium) rs1350028435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2358335,Human_RBP_ID_26777434 59548 RMVar_ID_59548 Human_SNP_ID_508129967 m1A Human chr12 + 79690921 79690921 79690921 GGGACGAGGCGTAGGGCTGGGATCCGGCTCCCAGGTGTGCCGAAGCTGGCGCGCGCTCTTCCGCC GGGACGAGGCGTAGGGCTGGGATCCGGCTCCCTGGTGTGCCGAAGCTGGCGCGCGCTCTTCCGCC A T AC073569.2 Ensembl:ENSG00000258048 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:79690843..79690997;chr12:79690854..79690976;chr12:79690860..79690997 26863196 MeRIP-seq:(Medium) rs1369085462 Functional Loss SNV dbSNP153 33..33 33 - - - 59549 RMVar_ID_59549 Human_SNP_ID_508129979 m1A Human chr12 - 79690948 79690948 79690948 GCGAGTTTGCCGCGGCACTTTCCGCGCGGCGGAAGAGCGCGCGCCAGCTTCGGCACACCTGGGAG GCGAGTTTGCCGCGGCACTTTCCGCGCGGCGGCAGAGCGCGCGCCAGCTTCGGCACACCTGGGAG T G PAWR Ensembl:ENSG00000177425 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:79690897..79690997 32194978 MeRIP-seq:(Medium) rs1281202674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1402311 59550 RMVar_ID_59550 Human_SNP_ID_508154967 m1A Human chr12 + 79795710 79795710 79795710 TCTCTTGGTCGTCGTCGTTCTCTGATTGATTTAGGTTGTGATTTATCTTCTCCTTCTTTCTCCTC TCTCTTGGTCGTCGTCGTTCTCTGATTGATTTGGGTTGTGATTTATCTTCTCCTTCTTTCTCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:79795626..79795775 26863196 MeRIP-seq:(Medium) rs747353858 Functional Loss SNV dbSNP153 33..33 33 - - - 59551 RMVar_ID_59551 Human_SNP_ID_508166603 m1A Human chr12 + 79844790 79844790 79844790 GTGATATGACCTCCTGCTACTTCTGTGACCTCATCTCCTTCCTGCCTCTTCCTCTGCTCTGCCTC GTGATATGACCTCCTGCTACTTCTGTGACCTCCTCTCCTTCCTGCCTCTTCCTCTGCTCTGCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79844787..79844969 26863196 MeRIP-seq:(Medium) rs532026038 Functional Loss SNV dbSNP153 33..33 33 - - - 59552 RMVar_ID_59552 Human_SNP_ID_508166604 m1A Human chr12 + 79844790 79844790 79844790 GTGATATGACCTCCTGCTACTTCTGTGACCTCATCTCCTTCCTGCCTCTTCCTCTGCTCTGCCTC GTGATATGACCTCCTGCTACTTCTGTGACCTCGTCTCCTTCCTGCCTCTTCCTCTGCTCTGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79844787..79844969 26863196 MeRIP-seq:(Medium) rs532026038 Functional Loss SNV dbSNP153 33..33 33 - - - 59553 RMVar_ID_59553 Human_SNP_ID_508166730 m1A Human chr12 + 79845354 79845354 79845354 TGAAGTAGCTCTTCCATTGCCTCCTCCTCCGCAATATCTAAAGGTGTATCTCCTTCACTGTTGAC TGAAGTAGCTCTTCCATTGCCTCCTCCTCCGCGATATCTAAAGGTGTATCTCCTTCACTGTTGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:79845267..79845400;chr12:79845258..79845360 26863196 MeRIP-seq:(Medium) rs1429294117 Functional Loss SNV dbSNP153 33..33 33 - - - 59554 RMVar_ID_59554 Human_SNP_ID_508184319 m1A Human chr12 - 79918640 79918640 79918640 ATGAACTAGCTTAGCGGCAGGAGGGTTGGAAAATAGTAGATGGACTTAAAATATATTTATGAAAT ATGAACTAGCTTAGCGGCAGGAGGGTTGGAAAGTAGTAGATGGACTTAAAATATATTTATGAAAT T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79918635..79918703 26863196 MeRIP-seq:(Medium) rs11114270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12044625 RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 59555 RMVar_ID_59555 Human_SNP_ID_508188421 m1A Human chr12 + 79934972 79934972 79934972 CTGCCGCCGGGTCTTCTTATCGCGAGGGGGGGAAGGGGGAGGCGGAGAGGGAAGAGAGGGGAGGC CTGCCGCCGGGTCTTCTTATCGCGAGGGGGGGGAGGGGGAGGCGGAGAGGGAAGAGAGGGGAGGC A G PPP1R12A-AS1 Ensembl:ENSG00000257557 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:79934933..79935125 26863196 MeRIP-seq:(Medium) rs1225173793 Functional Loss SNV dbSNP153 33..33 33 - - - 59556 RMVar_ID_59556 Human_SNP_ID_513148360 m1A Human chr12 + 100142827 100142819 100142828 CCGAGAACCCGGAGCATCACGCTCAGGCCGCCACGGCCGCCGCGGGCGCCATCTTGGCTGCAGCA CCGAGAACCCGGAGCATCACGCTCA_________GGCCGCCGCGGGCGCCATCTTGGCTGCAGCA AGGCCGCCAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:100142648..100142846 26863196 MeRIP-seq:(Medium) rs1344182791 Functional Loss DEL dbSNP153 26..34 33 - - - 59557 RMVar_ID_59557 Human_SNP_ID_513148370 m1A Human chr12 + 100142827 100142827 100142827 CCGAGAACCCGGAGCATCACGCTCAGGCCGCCACGGCCGCCGCGGGCGCCATCTTGGCTGCAGCA CCGAGAACCCGGAGCATCACGCTCAGGCCGCCGCGGCCGCCGCGGGCGCCATCTTGGCTGCAGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:100142648..100142846 26863196 MeRIP-seq:(Medium) rs1170776815 Functional Loss SNV dbSNP153 33..33 33 - - - 59558 RMVar_ID_59558 Human_SNP_ID_513152259 m1A Human chr12 - 100157253 100157252 100157253 CCCAGCGTCTGAGTCCTGTCCTCCTGCAGGAGAGTACATCGCACTGTACCAGAGCCAGAGGGCAG CCCAGCGTCTGAGTCCTGTCCTCCTGCAGGAG_GTACATCGCACTGTACCAGAGCCAGAGGGCAG CT C GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:100157203..100157401 26863196 MeRIP-seq:(Medium) rs758621760 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_874950 Human_Splice_Rec_1412613,Human_Splice_Rec_1412630,Human_Splice_Rec_1412631,Human_Splice_Rec_1412635,Human_Splice_Rec_1412645,Human_Splice_Rec_1412671 59559 RMVar_ID_59559 Human_SNP_ID_513152265 m1A Human chr12 - 100157258 100157258 100157258 GGGGCCCCAGCGTCTGAGTCCTGTCCTCCTGCAGGAGAGTACATCGCACTGTACCAGAGCCAGAG GGGGCCCCAGCGTCTGAGTCCTGTCCTCCTGCGGGAGAGTACATCGCACTGTACCAGAGCCAGAG T C GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:100157211..100157391 26863196 MeRIP-seq:(Medium) rs768247772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874950,Human_RBP_ID_3421070 Human_Splice_Rec_1412613,Human_Splice_Rec_1412631,Human_Splice_Rec_1412635,Human_Splice_Rec_1412645,Human_Splice_Rec_1412671 59560 RMVar_ID_59560 Human_SNP_ID_513152266 m1A Human chr12 - 100157258 100157258 100157258 GGGGCCCCAGCGTCTGAGTCCTGTCCTCCTGCAGGAGAGTACATCGCACTGTACCAGAGCCAGAG GGGGCCCCAGCGTCTGAGTCCTGTCCTCCTGCCGGAGAGTACATCGCACTGTACCAGAGCCAGAG T G GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:100157211..100157391 26863196 MeRIP-seq:(Medium) rs768247772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874950,Human_RBP_ID_3421070 Human_Splice_Rec_1412613,Human_Splice_Rec_1412631,Human_Splice_Rec_1412635,Human_Splice_Rec_1412645,Human_Splice_Rec_1412671 59561 RMVar_ID_59561 Human_SNP_ID_513154164 m1A Human chr12 - 100164132 100164132 100164132 GCTTCCAGGAACTCAGCCTGCACAGAGGCAGCAGTGACAAGGAGCCAGGCGCAGCACACCAGAGC GCTTCCAGGAACTCAGCCTGCACAGAGGCAGCGGTGACAAGGAGCCAGGCGCAGCACACCAGAGC T C GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:100164083..100164154 26863196 MeRIP-seq:(Medium) rs549078272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5556177,Human_RBP_ID_17205507 59562 RMVar_ID_59562 Human_SNP_ID_513154821 m1A Human chr12 - 100167120 100167120 100167120 ATTTTGGGCAGGTGTGCACATTGAGAGAGGAGAAGGAGGATAGCATGAGTTGGGTATAAGAACAG ATTTTGGGCAGGTGTGCACATTGAGAGAGGAGGAGGAGGATAGCATGAGTTGGGTATAAGAACAG T C GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:100166941..100167145;chr12:100166879..100167168 26863196 MeRIP-seq:(Medium) rs1387296169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5556187 RMVar_hsa_circ_101875,RMVar_hsa_circ_159147 59563 RMVar_ID_59563 Human_SNP_ID_513162379 m1A Human chr12 - 100199891 100199891 100199891 CTGAGAGAGGAGCGGGGCGGCGGGAAGGGGGCACCGCGGGGGCAGGGAGCGCAGCAGCCGCAGCG CTGAGAGAGGAGCGGGGCGGCGGGAAGGGGGCTCCGCGGGGGCAGGGAGCGCAGCAGCCGCAGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:100199588..100200000 26863196 MeRIP-seq:(Medium) rs1271482310 Functional Loss SNV dbSNP153 33..33 33 - - - 59564 RMVar_ID_59564 Human_SNP_ID_513178244 m1A Human chr12 - 100266981 100266981 100266981 AGACTTGTCAGTCAGAACGAGCTTCCGGGCCCAGGGCTGAACGGGCCAAGTTCCAGGAACCGTAG AGACTTGTCAGTCAGAACGAGCTTCCGGGCCCGGGGCTGAACGGGCCAAGTTCCAGGAACCGTAG T C DEPDC4 Ensembl:ENSG00000166153 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:100263854..100267030 26863410 MeRIP-seq:(Medium) rs138623297 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1412887,Human_Splice_Rec_1412915,Human_Splice_Rec_1412929,Human_Splice_Rec_1412939,Human_Splice_Rec_1412951,Human_Splice_Rec_1412959,Human_Splice_Rec_1412965 RMVar_hsa_circ_159160,RMVar_hsa_circ_98564 59565 RMVar_ID_59565 Human_SNP_ID_513178527 m1A Human chr12 - 100267443 100267441 100267443 CTCCTCGCCGGCTCCGGGAGCCCAGGCGAGAGAGCCGCCGGTGAGGGAGGTCGGTCGGTGCCGGC CTCCTCGCCGGCTCCGGGAGCCCAGGCGAGAG__CCGCCGGTGAGGGAGGTCGGTCGGTGCCGGC GCT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:100267401..100267675 26863196 MeRIP-seq:(Medium) rs1213972201 Functional Loss DEL dbSNP153 33..34 33 - - - 59566 RMVar_ID_59566 Human_SNP_ID_513178528 m1A Human chr12 - 100267443 100267443 100267443 CTCCTCGCCGGCTCCGGGAGCCCAGGCGAGAGAGCCGCCGGTGAGGGAGGTCGGTCGGTGCCGGC CTCCTCGCCGGCTCCGGGAGCCCAGGCGAGAGGGCCGCCGGTGAGGGAGGTCGGTCGGTGCCGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:100267401..100267675 26863196 MeRIP-seq:(Medium) rs1314892816 Functional Loss SNV dbSNP153 33..33 33 - - - 59567 RMVar_ID_59567 Human_SNP_ID_513178558 m1A Human chr12 - 100267550 100267550 100267550 GCCGACCGCCGATCGCCCGGCCGGCCGCCGGCAGGCCCGTCACCAGGCAACACCCACCAGCCTGA GCCGACCGCCGATCGCCCGGCCGGCCGCCGGCGGGCCCGTCACCAGGCAACACCCACCAGCCTGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:100267479..100267675 26863196 MeRIP-seq:(Medium) rs1245093718 Functional Loss SNV dbSNP153 33..33 33 - - - 59568 RMVar_ID_59568 Human_SNP_ID_513178563 m1A Human chr12 - 100267578 100267555 100267578 TGCTCGTCCAGCCCCGCTTTGCGCGGGCGCCGACCGCCGATCGCCCGGCCGGCCGCCGGCAGGCC TGCTCGTCCAGCCCCGCTTTGCGCGGGCGCCG_______________________CCGGCAGGCC GCGGCCGGCCGGGCGATCGGCGGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:100267401..100267625 26863196 MeRIP-seq:(Medium) rs974690377 Functional Loss DEL dbSNP153 33..55 33 - - - 59569 RMVar_ID_59569 Human_SNP_ID_513178585 m1A Human chr12 + 100267592 100267592 100267592 CGGCCGGGCGATCGGCGGTCGGCGCCCGCGCAAAGCGGGGCTGGACGAGCAGCGAGCTCCGGGGA CGGCCGGGCGATCGGCGGTCGGCGCCCGCGCAGAGCGGGGCTGGACGAGCAGCGAGCTCCGGGGA A G SCYL2 Ensembl:ENSG00000136021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:100267222..100267788 26863196 MeRIP-seq:(Medium) rs1003606488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159161 59570 RMVar_ID_59570 Human_SNP_ID_513178597 m1A Human chr12 + 100267624 100267624 100267624 AAGCGGGGCTGGACGAGCAGCGAGCTCCGGGGAGCGGATCCGAGAGGGCCGAGTCCTCGAAAGAG AAGCGGGGCTGGACGAGCAGCGAGCTCCGGGGGGCGGATCCGAGAGGGCCGAGTCCTCGAAAGAG A G SCYL2 Ensembl:ENSG00000136021 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:100267501..100267730 26863196 MeRIP-seq:(Medium) rs1053468874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22910577 RMVar_hsa_circ_159161 59571 RMVar_ID_59571 Human_SNP_ID_513195324 m1A Human chr12 + 100335881 100335881 100335881 TCTGACTGGCAGTGAGTCCGAAAATAAAGAGGACGGGTTACAGAATAAACATAAAAGAGTGAGTT TCTGACTGGCAGTGAGTCCGAAAATAAAGAGGGCGGGTTACAGAATAAACATAAAAGAGTGAGTT A G SCYL2 Ensembl:ENSG00000136021 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:100335751..100335885 32194978 MeRIP-seq:(Medium) rs771019650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1413000,Human_Splice_Rec_1413001,Human_Splice_Rec_1413040,Human_Splice_Rec_1413041,Human_Splice_Rec_1413076,Human_Splice_Rec_1413077,Human_Splice_Rec_1413110,Human_Splice_Rec_1413111,Human_Splice_Rec_1413113 RMVar_hsa_circ_360986,RMVar_hsa_circ_64872 59572 RMVar_ID_59572 Human_SNP_ID_513348867 m1A Human chr12 + 100990060 100990060 100990060 GATGGATGAATAGATACATGGATGGGTATAGGAGTGGTTGTGTAGGTGTATAAATGAATAGAGGA GATGGATGAATAGATACATGGATGGGTATAGGCGTGGTTGTGTAGGTGTATAAATGAATAGAGGA A C ANO4 Ensembl:ENSG00000151572 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:100990016..100990087 26863196 MeRIP-seq:(Medium) rs147791840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1222,RMVar_hsa_circ_39813,RMVar_hsa_circ_15801,RMVar_hsa_circ_37792,RMVar_hsa_circ_18004,RMVar_hsa_circ_29557,RMVar_hsa_circ_319067,RMVar_hsa_circ_325743,RMVar_hsa_circ_325021,RMVar_hsa_circ_282348,RMVar_hsa_circ_159208,RMVar_hsa_circ_22987,RMVar_hsa_circ_159209,RMVar_hsa_circ_159207,RMVar_hsa_circ_3855 59573 RMVar_ID_59573 Human_SNP_ID_513419866 m1A Human chr12 + 101280193 101280192 101280193 GAGAAAGTCTGGGCATCTGGGAATCGGAGAGTATAGCCTGTGAGCCGCTTTCCCCTCCTTACTGT GAGAAAGTCTGGGCATCTGGGAATCGGAGAGT_TAGCCTGTGAGCCGCTTTCCCCTCCTTACTGT TA T UTP20 Ensembl:ENSG00000120800 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:101280142..101280243 26863196 MeRIP-seq:(Medium) rs1250796310 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4196193,Human_RBP_ID_6119230,Human_RBP_ID_8786866,Human_RBP_ID_9279747 59574 RMVar_ID_59574 Human_SNP_ID_513425544 m1A Human chr12 + 101303385 101303385 101303385 AGAAAAACAAAGCAGGGTCAGGAGATAGGGAGAGTCCAGAGGTGAGGGGAGCGGTAGCAGTTTTA AGAAAAACAAAGCAGGGTCAGGAGATAGGGAGTGTCCAGAGGTGAGGGGAGCGGTAGCAGTTTTA A T UTP20 Ensembl:ENSG00000120800 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:101303352..101303500 26863196 MeRIP-seq:(Medium) rs767256667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28847,RMVar_hsa_circ_67587,RMVar_hsa_circ_123108,RMVar_hsa_circ_159235,RMVar_hsa_circ_110546,RMVar_hsa_circ_159239,RMVar_hsa_circ_101035,RMVar_hsa_circ_18254,RMVar_hsa_circ_359899,RMVar_hsa_circ_51741,RMVar_hsa_circ_121557,RMVar_hsa_circ_95319,RMVar_hsa_circ_65437,RMVar_hsa_circ_159242,RMVar_hsa_circ_369630,RMVar_hsa_circ_159243,RMVar_hsa_circ_159244,RMVar_hsa_circ_265543,RMVar_hsa_circ_159245 59575 RMVar_ID_59575 Human_SNP_ID_513524977 m1A Human chr12 + 101697557 101697557 101697557 TAACAAGTTGCCGTTGGCGGGCGCCGAGGGTGACCCGCGAGCGCGGCACCCGCCTCCCCGCCCCT TAACAAGTTGCCGTTGGCGGGCGCCGAGGGTGTCCCGCGAGCGCGGCACCCGCCTCCCCGCCCCT A T CHPT1 Ensembl:ENSG00000111666 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:101697511..101697619 26863196 MeRIP-seq:(Medium) rs970230547 Functional Loss SNV dbSNP153 33..33 33 - - - 59576 RMVar_ID_59576 Human_SNP_ID_513525078 m1A Human chr12 - 101697724 101697724 101697724 GGCTGGACTCACCGGTCGGGCCCGCACGGCGGAGGTCGAGGTCAGGCCGGCCTGCCCGGCTGCCG GGCTGGACTCACCGGTCGGGCCCGCACGGCGGTGGTCGAGGTCAGGCCGGCCTGCCCGGCTGCCG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:101697676..101697931 26863196 MeRIP-seq:(Medium) rs1447190687 Functional Loss SNV dbSNP153 33..33 33 - - - 59577 RMVar_ID_59577 Human_SNP_ID_513537008 m1A Human chr12 - 101748639 101748637 101748640 AGCTCCCATTTATCTTTCTTTCAATCGCTAGGAGTTCTCCCTCCTCTCTCCTCCTTCCTCCTCTC AGCTCCCATTTATCTTTCTTTCAATCGCTAG___TTCTCCCTCCTCTCTCCTCCTTCCTCCTCTC ACTC A GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:101748613..101748698 26863196 MeRIP-seq:(Medium) rs1265409413 Functional Loss DEL dbSNP153 32..34 33 - - - 59578 RMVar_ID_59578 Human_SNP_ID_513557233 m1A Human chr12 + 101830691 101830686 101830691 AGGAGCTTGAACAGCATCACCCCTTCACCGCCACGCCACGCCCCGAGGAGCCTGAGCCGCCGCCG AGGAGCTTGAACAGCATCACCCCTTCAC_____CGCCACGCCCCGAGGAGCCTGAGCCGCCGCCG CCGCCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:101830588..101830888 26863196 MeRIP-seq:(Medium) rs745871394 Functional Loss DEL dbSNP153 29..33 33 - - - 59579 RMVar_ID_59579 Human_SNP_ID_513557237 m1A Human chr12 + 101830691 101830691 101830691 AGGAGCTTGAACAGCATCACCCCTTCACCGCCACGCCACGCCCCGAGGAGCCTGAGCCGCCGCCG AGGAGCTTGAACAGCATCACCCCTTCACCGCCGCGCCACGCCCCGAGGAGCCTGAGCCGCCGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:101830588..101830888 26863196 MeRIP-seq:(Medium) rs1454693486 Functional Loss SNV dbSNP153 33..33 33 - - - 59580 RMVar_ID_59580 Human_SNP_ID_513557245 m1A Human chr12 + 101830704 101830704 101830704 GCATCACCCCTTCACCGCCACGCCACGCCCCGAGGAGCCTGAGCCGCCGCCGCCGCCGCCGCCGC GCATCACCCCTTCACCGCCACGCCACGCCCCGCGGAGCCTGAGCCGCCGCCGCCGCCGCCGCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:101830657..101830846 26863196 MeRIP-seq:(Medium) rs778784398 Functional Loss SNV dbSNP153 33..33 33 - - - 59581 RMVar_ID_59581 Human_SNP_ID_513557252 m1A Human chr12 - 101830711 101830711 101830711 CGCTGAGGCGGCGGCGGCGGCGGCGGCGGCTCAGGCTCCTCGGGGCGTGGCGTGGCGGTGAAGGG CGCTGAGGCGGCGGCGGCGGCGGCGGCGGCTCCGGCTCCTCGGGGCGTGGCGTGGCGGTGAAGGG T G GNPTAB Ensembl:ENSG00000111670 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:101830669..101830820 26863196 MeRIP-seq:(Medium) rs1566106063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_408132,Human_RBP_ID_4246254,Human_RBP_ID_9279760 59582 RMVar_ID_59582 Human_SNP_ID_513569011 m1A Human chr12 + 101877407 101877407 101877407 GCCAGTGACCCCACGCCGCCCGTCCGCGCCCAACCCGGCCTCCGCCGAGTGTCCAAACCAAAAGC GCCAGTGACCCCACGCCGCCCGTCCGCGCCCATCCCGGCCTCCGCCGAGTGTCCAAACCAAAAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:101877391..101877496 26863196 MeRIP-seq:(Medium) rs1314743271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_121372,RMVar_hsa_circ_101936,RMVar_hsa_circ_159311,RMVar_hsa_circ_159312,RMVar_hsa_circ_159310 59583 RMVar_ID_59583 Human_SNP_ID_513569084 m1A Human chr12 - 101877640 101877640 101877640 CTCCGCGACGGCCGGGGCAGGCCCAGCCCCGGAGGGAGGGGAAGCGCGAGGAGCGGAGCGAGGCT CTCCGCGACGGCCGGGGCAGGCCCAGCCCCGGGGGGAGGGGAAGCGCGAGGAGCGGAGCGAGGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr12:101877549..101877762;chr12:101877382..101877748 26863196 MeRIP-seq:(Medium) rs1170406032 Functional Loss SNV dbSNP153 33..33 33 - - - 59584 RMVar_ID_59584 Human_SNP_ID_513569090 m1A Human chr12 - 101877654 101877654 101877654 GGTGGGAGGGGAGGCTCCGCGACGGCCGGGGCAGGCCCAGCCCCGGAGGGAGGGGAAGCGCGAGG GGTGGGAGGGGAGGCTCCGCGACGGCCGGGGCGGGCCCAGCCCCGGAGGGAGGGGAAGCGCGAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:101877609..101877786 26863196 MeRIP-seq:(Medium) rs888554714 Functional Loss SNV dbSNP153 33..33 33 - - - 59585 RMVar_ID_59585 Human_SNP_ID_513569256 m1A Human chr12 - 101878013 101878013 101878013 CTCCCACCTCTGCCTGACCACACGACGCCCCAAGCTGGGTCCGGACGCCTTCCCTCCCCGTCGGC CTCCCACCTCTGCCTGACCACACGACGCCCCAGGCTGGGTCCGGACGCCTTCCCTCCCCGTCGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:101877962..101878210 26863196 MeRIP-seq:(Medium) rs1453824201 Functional Loss SNV dbSNP153 33..33 33 - - - 59586 RMVar_ID_59586 Human_SNP_ID_513612585 m1A Human chr12 + 102061969 102061969 102061969 ATGAGAGGAAGCCCGTCCTCATCCATCTCCTCAGCGGGCGGTGGACCCCGAGTTCACCCACAAAC ATGAGAGGAAGCCCGTCCTCATCCATCTCCTCCGCGGGCGGTGGACCCCGAGTTCACCCACAAAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:102061901..102062026 26863196 MeRIP-seq:(Medium) rs536060529 Functional Loss SNV dbSNP153 33..33 33 - - - 59587 RMVar_ID_59587 Human_SNP_ID_513612586 m1A Human chr12 + 102061969 102061969 102061969 ATGAGAGGAAGCCCGTCCTCATCCATCTCCTCAGCGGGCGGTGGACCCCGAGTTCACCCACAAAC ATGAGAGGAAGCCCGTCCTCATCCATCTCCTCGGCGGGCGGTGGACCCCGAGTTCACCCACAAAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:102061901..102062026 26863196 MeRIP-seq:(Medium) rs536060529 Functional Loss SNV dbSNP153 33..33 33 - - - 59588 RMVar_ID_59588 Human_SNP_ID_513612595 m1A Human chr12 - 102061990 102061980 102061991 GGCGGGCCCCATCTGGGAGGGGTTTGTGGGTGAACTCGGGGTCCACCGCCCGCTGAGGAGATGGA GGCGGGCCCCATCTGGGAGGGGTTTGTGGGT___________CCACCGCCCGCTGAGGAGATGGA GACCCCGAGTTC G WASHC3 Ensembl:ENSG00000120860 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:102061919..102062069 26863196 MeRIP-seq:(Medium) rs1189279758 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_408161,Human_RBP_ID_4246922,Human_RBP_ID_5315031,Human_RBP_ID_9352766,Human_RBP_ID_18417314 Human_Splice_Rec_1415053,Human_Splice_Rec_1415065,Human_Splice_Rec_1415079,Human_Splice_Rec_1415093,Human_Splice_Rec_1415105,Human_Splice_Rec_1415119,Human_Splice_Rec_1415157,Human_Splice_Rec_1415167,Human_Splice_Rec_1415175,Human_Splice_Rec_1415181 59589 RMVar_ID_59589 Human_SNP_ID_514044873 m1A Human chr12 - 103841145 103841145 103841145 TGGCGGCAGCAGGCAGCAGGCATGACCATGGCAGCGGCGGCGGTGGTGGCACGCGGGGCCGGGGC TGGCGGCAGCAGGCAGCAGGCATGACCATGGCCGCGGCGGCGGTGGTGGCACGCGGGGCCGGGGC T G NT5DC3 Ensembl:ENSG00000111696 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:103841026..103841250 26863196 MeRIP-seq:(Medium) rs1014915641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246928,Human_RBP_ID_18417496 59590 RMVar_ID_59590 Human_SNP_ID_514044901 m1A Human chr12 - 103841201 103841201 103841201 GAGCGCGGGTAGATCTTGGGCCGGGCAGCAGCAGTCGCAGAGCGGCGCGGCGGCGGTGGCGGCAG GAGCGCGGGTAGATCTTGGGCCGGGCAGCAGCTGTCGCAGAGCGGCGCGGCGGCGGTGGCGGCAG T A NT5DC3 Ensembl:ENSG00000111696 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:103841013..103841219 26863196 MeRIP-seq:(Medium) rs912214043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4197020 59591 RMVar_ID_59591 Human_SNP_ID_514044902 m1A Human chr12 - 103841201 103841201 103841201 GAGCGCGGGTAGATCTTGGGCCGGGCAGCAGCAGTCGCAGAGCGGCGCGGCGGCGGTGGCGGCAG GAGCGCGGGTAGATCTTGGGCCGGGCAGCAGCGGTCGCAGAGCGGCGCGGCGGCGGTGGCGGCAG T C NT5DC3 Ensembl:ENSG00000111696 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:103841013..103841219 26863196 MeRIP-seq:(Medium) rs912214043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4197020 59592 RMVar_ID_59592 Human_SNP_ID_514065673 m1A Human chr12 - 103930474 103930474 103930474 CCGGTGAGTCTCAAGTCCCCTTCGATCGCAGGAGCCGCCTCCACCCCCCACCCCTGGGTTCGGAT CCGGTGAGTCTCAAGTCCCCTTCGATCGCAGGTGCCGCCTCCACCCCCCACCCCTGGGTTCGGAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:103930376..103930629;chr12:103930367..103930631;chr12:103930376..103930630;chr12:103930376..103931625 26863196 MeRIP-seq:(Medium) rs760496952 Functional Loss SNV dbSNP153 33..33 33 - - - 59593 RMVar_ID_59593 Human_SNP_ID_514065674 m1A Human chr12 - 103930474 103930474 103930474 CCGGTGAGTCTCAAGTCCCCTTCGATCGCAGGAGCCGCCTCCACCCCCCACCCCTGGGTTCGGAT CCGGTGAGTCTCAAGTCCCCTTCGATCGCAGGGGCCGCCTCCACCCCCCACCCCTGGGTTCGGAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:103930376..103930629;chr12:103930367..103930631;chr12:103930376..103930630;chr12:103930376..103931625 26863196 MeRIP-seq:(Medium) rs760496952 Functional Loss SNV dbSNP153 33..33 33 - - - 59594 RMVar_ID_59594 Human_SNP_ID_514065690 m1A Human chr12 - 103930494 103930494 103930494 AGGGCCCTCATGGCGTGCGGCCGGTGAGTCTCAAGTCCCCTTCGATCGCAGGAGCCGCCTCCACC AGGGCCCTCATGGCGTGCGGCCGGTGAGTCTCCAGTCCCCTTCGATCGCAGGAGCCGCCTCCACC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:103930426..103930575;chr12:103930401..103930575 32194978 MeRIP-seq:(Medium) rs1427908536 Functional Loss SNV dbSNP153 33..33 33 - - - 59595 RMVar_ID_59595 Human_SNP_ID_514066187 m1A Human chr12 - 103932292 103932292 103932292 CTTATTTGTGATGCATTTAATCCATCCAACTGAATAGCTTCTTCCTCTCTAAGGAAATCAGTTAG CTTATTTGTGATGCATTTAATCCATCCAACTGTATAGCTTCTTCCTCTCTAAGGAAATCAGTTAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:103932276..103932425 32194978 MeRIP-seq:(Medium) rs774680935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6122342 59596 RMVar_ID_59596 Human_SNP_ID_514067533 m1A Human chr12 - 103938405 103938405 103938405 TCTTCTTCTTCTTCCTCTACTGCAGCTTCATCATCAGATTCTTCTTTCTCTTCTTTGGCTGCTTC TCTTCTTCTTCTTCCTCTACTGCAGCTTCATCGTCAGATTCTTCTTTCTCTTCTTTGGCTGCTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:103938317..103938503 26863196 MeRIP-seq:(Medium) rs772361512 Functional Loss SNV dbSNP153 33..33 33 - - - 59597 RMVar_ID_59597 Human_SNP_ID_514068803 m1A Human chr12 - 103943729 103943729 103943729 CTGAGACACCACAGCCTTTTCAATCTTAGGGAAAGAAATCAAGTCATATAAATTAATATCAACAG CTGAGACACCACAGCCTTTTCAATCTTAGGGACAGAAATCAAGTCATATAAATTAATATCAACAG T G C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:103943726..103943875 32194978 MeRIP-seq:(Medium) rs1440291118 Functional Loss SNV dbSNP153 33..33 33 - - - 59598 RMVar_ID_59598 Human_SNP_ID_514069604 m1A Human chr12 - 103946932 103946932 103946932 GCGGGAAGGTTGGGGATACAAACCTTTGCATCAGGGTCAATGTTCAAACTGAGGCGAAGCATTCT GCGGGAAGGTTGGGGATACAAACCTTTGCATCGGGGTCAATGTTCAAACTGAGGCGAAGCATTCT T C C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:103946876..103946950 26863196 MeRIP-seq:(Medium) rs777596873 Functional Loss SNV dbSNP153 33..33 33 - - - 59599 RMVar_ID_59599 Human_SNP_ID_514069605 m1A Human chr12 - 103946932 103946932 103946932 GCGGGAAGGTTGGGGATACAAACCTTTGCATCAGGGTCAATGTTCAAACTGAGGCGAAGCATTCT GCGGGAAGGTTGGGGATACAAACCTTTGCATCCGGGTCAATGTTCAAACTGAGGCGAAGCATTCT T G C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:103946876..103946950 26863196 MeRIP-seq:(Medium) rs777596873 Functional Loss SNV dbSNP153 33..33 33 - - - 59600 RMVar_ID_59600 Human_SNP_ID_514069610 m1A Human chr12 + 103946939 103946939 103946939 TTCGCCTCAGTTTGAACATTGACCCTGATGCAAAGGTTTGTATCCCCAACCTTCCCGCAAAGGCT TTCGCCTCAGTTTGAACATTGACCCTGATGCACAGGTTTGTATCCCCAACCTTCCCGCAAAGGCT A C HSP90B1 Ensembl:ENSG00000166598 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:103946816..103946987;chr12:103946842..103946978 26863196 MeRIP-seq:(Medium) rs1566168803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229149,Human_RBP_ID_811096,Human_RBP_ID_877723,Human_RBP_ID_9365468,Human_RBP_ID_22756942,Human_RBP_ID_22910607,Human_RBP_ID_24543149,Human_RBP_ID_26321926,Human_RBP_ID_27805916 Human_Splice_Rec_1416371,Human_Splice_Rec_1416417,Human_Splice_Rec_1416433,Human_Splice_Rec_1416439 RMVar_hsa_circ_2770,RMVar_hsa_circ_121104,RMVar_hsa_circ_86096,RMVar_hsa_circ_159351,RMVar_hsa_circ_159355,RMVar_hsa_circ_70954,RMVar_hsa_circ_81709,RMVar_hsa_circ_159359,RMVar_hsa_circ_98686,RMVar_hsa_circ_117640,RMVar_hsa_circ_159360,RMVar_hsa_circ_108143,RMVar_hsa_circ_159361,RMVar_hsa_circ_91683,RMVar_hsa_circ_159362,RMVar_hsa_circ_159363 59601 RMVar_ID_59601 Human_SNP_ID_514069611 m1A Human chr12 + 103946940 103946940 103946940 TCGCCTCAGTTTGAACATTGACCCTGATGCAAAGGTTTGTATCCCCAACCTTCCCGCAAAGGCTG TCGCCTCAGTTTGAACATTGACCCTGATGCAATGGTTTGTATCCCCAACCTTCCCGCAAAGGCTG A T HSP90B1 Ensembl:ENSG00000166598 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:103946832..103946962 26863196 MeRIP-seq:(Medium) rs1220841786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229149,Human_RBP_ID_811096,Human_RBP_ID_877723,Human_RBP_ID_9365468,Human_RBP_ID_22756942,Human_RBP_ID_22910607,Human_RBP_ID_24543149,Human_RBP_ID_26321926,Human_RBP_ID_27805916 Human_Splice_Rec_1416371,Human_Splice_Rec_1416417,Human_Splice_Rec_1416433,Human_Splice_Rec_1416439 RMVar_hsa_circ_2770,RMVar_hsa_circ_121104,RMVar_hsa_circ_86096,RMVar_hsa_circ_159351,RMVar_hsa_circ_159355,RMVar_hsa_circ_70954,RMVar_hsa_circ_81709,RMVar_hsa_circ_159359,RMVar_hsa_circ_98686,RMVar_hsa_circ_117640,RMVar_hsa_circ_159360,RMVar_hsa_circ_108143,RMVar_hsa_circ_159361,RMVar_hsa_circ_91683,RMVar_hsa_circ_159362,RMVar_hsa_circ_159363 59602 RMVar_ID_59602 Human_SNP_ID_514069735 m1A Human chr12 + 103947370 103947370 103947370 GAAGAGACAGCAGAAGACACAACAGAAGACACAGAGCAAGACGAAGATGAAGAAATGGATGTGGG GAAGAGACAGCAGAAGACACAACAGAAGACACGGAGCAAGACGAAGATGAAGAAATGGATGTGGG A G HSP90B1 Ensembl:ENSG00000166598 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:103947335..103947638 26863196 MeRIP-seq:(Medium) rs763219647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35274,Human_RBP_ID_811097,Human_RBP_ID_874990,Human_RBP_ID_1785203,Human_RBP_ID_2299194,Human_RBP_ID_4248936,Human_RBP_ID_5171819,Human_RBP_ID_5554514,Human_RBP_ID_6122425,Human_RBP_ID_8247443,Human_RBP_ID_9344683,Human_RBP_ID_9366860,Human_RBP_ID_17467538,Human_RBP_ID_18206207,Human_RBP_ID_18469235,Human_RBP_ID_18526421,Human_RBP_ID_22756948,Human_RBP_ID_22910610,Human_RBP_ID_24543155,Human_RBP_ID_24551242,Human_RBP_ID_24557754,Human_RBP_ID_24922297,Human_RBP_ID_26323302,Human_RBP_ID_26900018,Human_RBP_ID_27417870,Human_RBP_ID_27805920 Human_Splice_Rec_1416372,Human_Splice_Rec_1416373,Human_Splice_Rec_1416387,Human_Splice_Rec_1416418,Human_Splice_Rec_1416419,Human_Splice_Rec_1416434,Human_Splice_Rec_1416440,Human_Splice_Rec_1416441 Human_miRNA_ID_2611403,Human_miRNA_ID_2907871,Human_miRNA_ID_3026709 RMVar_hsa_circ_2770,RMVar_hsa_circ_121104,RMVar_hsa_circ_86096,RMVar_hsa_circ_159351,RMVar_hsa_circ_159355,RMVar_hsa_circ_70954,RMVar_hsa_circ_81709,RMVar_hsa_circ_159359,RMVar_hsa_circ_98686,RMVar_hsa_circ_117640,RMVar_hsa_circ_159360,RMVar_hsa_circ_108143,RMVar_hsa_circ_159361,RMVar_hsa_circ_91683,RMVar_hsa_circ_159362,RMVar_hsa_circ_308009,RMVar_hsa_circ_159363 59603 RMVar_ID_59603 Human_SNP_ID_514069736 m1A Human chr12 + 103947370 103947370 103947370 GAAGAGACAGCAGAAGACACAACAGAAGACACAGAGCAAGACGAAGATGAAGAAATGGATGTGGG GAAGAGACAGCAGAAGACACAACAGAAGACACTGAGCAAGACGAAGATGAAGAAATGGATGTGGG A T HSP90B1 Ensembl:ENSG00000166598 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:103947335..103947638 26863196 MeRIP-seq:(Medium) rs763219647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35274,Human_RBP_ID_811097,Human_RBP_ID_874990,Human_RBP_ID_1785203,Human_RBP_ID_2299194,Human_RBP_ID_4248936,Human_RBP_ID_5171819,Human_RBP_ID_5554514,Human_RBP_ID_6122425,Human_RBP_ID_8247443,Human_RBP_ID_9344683,Human_RBP_ID_9366860,Human_RBP_ID_17467538,Human_RBP_ID_18206207,Human_RBP_ID_18469235,Human_RBP_ID_18526421,Human_RBP_ID_22756948,Human_RBP_ID_22910610,Human_RBP_ID_24543155,Human_RBP_ID_24551242,Human_RBP_ID_24557754,Human_RBP_ID_24922297,Human_RBP_ID_26323302,Human_RBP_ID_26900018,Human_RBP_ID_27417870,Human_RBP_ID_27805920 Human_Splice_Rec_1416372,Human_Splice_Rec_1416373,Human_Splice_Rec_1416387,Human_Splice_Rec_1416418,Human_Splice_Rec_1416419,Human_Splice_Rec_1416434,Human_Splice_Rec_1416440,Human_Splice_Rec_1416441 Human_miRNA_ID_2611403,Human_miRNA_ID_2907871,Human_miRNA_ID_3026709 RMVar_hsa_circ_2770,RMVar_hsa_circ_121104,RMVar_hsa_circ_86096,RMVar_hsa_circ_159351,RMVar_hsa_circ_159355,RMVar_hsa_circ_70954,RMVar_hsa_circ_81709,RMVar_hsa_circ_159359,RMVar_hsa_circ_98686,RMVar_hsa_circ_117640,RMVar_hsa_circ_159360,RMVar_hsa_circ_108143,RMVar_hsa_circ_159361,RMVar_hsa_circ_91683,RMVar_hsa_circ_159362,RMVar_hsa_circ_308009,RMVar_hsa_circ_159363 59604 RMVar_ID_59604 Human_SNP_ID_514069796 m1A Human chr12 - 103947592 103947591 103947592 AAATAAAAAAAACCCAGAAGGTATTAAAAGTTAGCAGAAAAAAAACCTAGCTCACAGGTTTGTGC AAATAAAAAAAACCCAGAAGGTATTAAAAGTT_GCAGAAAAAAAACCTAGCTCACAGGTTTGTGC CT C C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:103947588..103947714 26863196 MeRIP-seq:(Medium) rs778090698 Functional Loss DEL dbSNP153 33..33 33 - - - 59605 RMVar_ID_59605 Human_SNP_ID_514069797 m1A Human chr12 - 103947592 103947592 103947592 AAATAAAAAAAACCCAGAAGGTATTAAAAGTTAGCAGAAAAAAAACCTAGCTCACAGGTTTGTGC AAATAAAAAAAACCCAGAAGGTATTAAAAGTTCGCAGAAAAAAAACCTAGCTCACAGGTTTGTGC T G C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:103947588..103947714 26863196 MeRIP-seq:(Medium) rs774603610 Functional Loss SNV dbSNP153 33..33 33 - - - 59606 RMVar_ID_59606 Human_SNP_ID_514069803 m1A Human chr12 - 103947606 103947606 103947606 AGATTCCTGTAAATAAATAAAAAAAACCCAGAAGGTATTAAAAGTTAGCAGAAAAAAAACCTAGC AGATTCCTGTAAATAAATAAAAAAAACCCAGACGGTATTAAAAGTTAGCAGAAAAAAAACCTAGC T G C12orf73 Ensembl:ENSG00000204954 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:103947603..103947742 26863196 MeRIP-seq:(Medium) rs761158438 Functional Loss SNV dbSNP153 33..33 33 - - - 59607 RMVar_ID_59607 Human_SNP_ID_514072091 m1A Human chr12 - 103957094 103957094 103957094 TAGAGCGCGTGTATAGAGGCAGAGAGGAGTGAAGTCCACAGTTCCTCTCCTCCAAGAGGTAGAAG TAGAGCGCGTGTATAGAGGCAGAGAGGAGTGAGGTCCACAGTTCCTCTCCTCCAAGAGGTAGAAG T C C12orf73 Ensembl:ENSG00000204954 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:103957076..103957180 26863410 MeRIP-seq:(Medium) rs1267041889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246931 Human_Splice_Rec_1416447,Human_Splice_Rec_1416455,Human_Splice_Rec_1416467,Human_Splice_Rec_1416491,Human_Splice_Rec_1416495 59608 RMVar_ID_59608 Human_SNP_ID_514072115 m1A Human chr12 - 103957158 103957158 103957158 GTCCGCTCCGTCCGCCCTTAGACCTGTTGCCCAGCATCCCTGCAGTTCGCGGTACAGTCTCTAGT GTCCGCTCCGTCCGCCCTTAGACCTGTTGCCCGGCATCCCTGCAGTTCGCGGTACAGTCTCTAGT T C C12orf73 Ensembl:ENSG00000204954 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:103957022..103957186 26863196 MeRIP-seq:(Medium) rs929477541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1785223,Human_RBP_ID_4246931,Human_RBP_ID_9323194,Human_RBP_ID_11785848,Human_RBP_ID_23532595 Human_Splice_Rec_1416447,Human_Splice_Rec_1416455,Human_Splice_Rec_1416467,Human_Splice_Rec_1416475,Human_Splice_Rec_1416491,Human_Splice_Rec_1416495 59609 RMVar_ID_59609 Human_SNP_ID_514074349 m1A Human chr12 + 103965605 103965605 103965605 AATGCTGATAAGCGTCATCATCCCATATACACAGCACCCCAAGGACAGCACCCTATCGCCCACGC AATGCTGATAAGCGTCATCATCCCATATACACGGCACCCCAAGGACAGCACCCTATCGCCCACGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:103965584..103965687 26863196 MeRIP-seq:(Medium) rs1223600236 Functional Loss SNV dbSNP153 33..33 33 - - - 59610 RMVar_ID_59610 Human_SNP_ID_514074486 m1A Human chr12 + 103965899 103965899 103965899 ACGGTAGAAGCCTGGAGGAGGAGCTTGAGTCCAGCCACTGTCTGGGTACTGCCAGCCATCGGGCC ACGGTAGAAGCCTGGAGGAGGAGCTTGAGTCCGGCCACTGTCTGGGTACTGCCAGCCATCGGGCC A G TDG Ensembl:ENSG00000139372 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:103965851..103966010;chr12:103965851..103967894 26863196 MeRIP-seq:(Medium) rs112179075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229034,Human_RBP_ID_877662,Human_RBP_ID_9322669,Human_RBP_ID_18410730,Human_RBP_ID_18417322,Human_RBP_ID_22039513,Human_RBP_ID_26321932 RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 59611 RMVar_ID_59611 Human_SNP_ID_514074545 m1A Human chr12 + 103966011 103966011 103966011 AGAGACCGGCTGCCCGTGTGCCCGGCAGGTGGAGCCGCCCGCATCAGCGGCCTCGGGGAATGGAA AGAGACCGGCTGCCCGTGTGCCCGGCAGGTGGTGCCGCCCGCATCAGCGGCCTCGGGGAATGGAA A T TDG Ensembl:ENSG00000139372 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:103965923..103966057 26863196 MeRIP-seq:(Medium) rs1247360088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246932 Human_Splice_Rec_1416497,Human_Splice_Rec_1416507,Human_Splice_Rec_1416509,Human_Splice_Rec_1416529,Human_Splice_Rec_1416545,Human_Splice_Rec_1416563,Human_Splice_Rec_1416575 RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 59612 RMVar_ID_59612 Human_SNP_ID_514077784 m1A Human chr12 - 103978199 103978195 103978199 CCATTAGCCATGGCTAGGTAATTCTACCTCCTAAGTGTTTCCTAATTCTTTCTCCACCCCTTCAG CCATTAGCCATGGCTAGGTAATTCTACCTCCT____GTTTCCTAATTCTTTCTCCACCCCTTCAG CACTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:103978196..103978314 26863196 MeRIP-seq:(Medium) rs1045443611 Functional Loss DEL dbSNP153 33..36 33 - - - 59613 RMVar_ID_59613 Human_SNP_ID_514100065 m1A Human chr12 + 104064635 104064635 104064635 TTCACGGGGCCGGTCCCCCGCGCCCGGCACGGACACCGAGCGGTGGCCATCCGGGAGCTGATGAT TTCACGGGGCCGGTCCCCCGCGCCCGGCACGGGCACCGAGCGGTGGCCATCCGGGAGCTGATGAT A G HCFC2 Ensembl:ENSG00000111727 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:104064588..104064673 26863196 MeRIP-seq:(Medium) rs774982958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4197257,Human_RBP_ID_5522149 Human_Splice_Rec_1416687,Human_Splice_Rec_1416715 59614 RMVar_ID_59614 Human_SNP_ID_514115947 m1A Human chr12 - 104137889 104137889 104137889 GCTCTTTGTGCGCCGGGCTGAGGAGCGGCGGGACGCGGGCCAGGCCACCTCACCCTCGCCGCCGT GCTCTTTGTGCGCCGGGCTGAGGAGCGGCGGGTCGCGGGCCAGGCCACCTCACCCTCGCCGCCGT T A NFYB Ensembl:ENSG00000120837 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:104137458..104138100 26863196 MeRIP-seq:(Medium) rs1241872252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18457286 59615 RMVar_ID_59615 Human_SNP_ID_514135926 m1A Human chr12 + 104221810 104221810 104221810 CTGAGCTGGGCAGGTGGTGGGAAGTTGTATAGACCCAGAAATAACTTGTTATGGGAAGAATTAAG CTGAGCTGGGCAGGTGGTGGGAAGTTGTATAGGCCCAGAAATAACTTGTTATGGGAAGAATTAAG A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:104221796..104221879 26863196 MeRIP-seq:(Medium) rs990866749 Functional Loss SNV dbSNP153 33..33 33 - - - 59616 RMVar_ID_59616 Human_SNP_ID_514146633 m1A Human chr12 + 104265339 104265339 104265339 CCATGAAGGCCTCGGGCACGCTACGAGAGTACAAGGTAGTGGGTCGCTGCCTGCCCACCCCCAAA CCATGAAGGCCTCGGGCACGCTACGAGAGTACGAGGTAGTGGGTCGCTGCCTGCCCACCCCCAAA A G RPL18AP3,TXNRD1 Ensembl:ENSG00000213442,Ensembl:ENSG00000198431 Pseudogene,Protein coding exon,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:104265285..104265390 26863410 MeRIP-seq:(Medium) rs1565868793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230243,Human_RBP_ID_408645,Human_RBP_ID_989294,Human_RBP_ID_1463140,Human_RBP_ID_1785299,Human_RBP_ID_3390687,Human_RBP_ID_4197329,Human_RBP_ID_8363433,Human_RBP_ID_17358025,Human_RBP_ID_17475210,Human_RBP_ID_18616050,Human_RBP_ID_23532832 Human_miRNA_ID_1818782,Human_miRNA_ID_1894309,Human_miRNA_ID_1894353,Human_miRNA_ID_1907801 RMVar_hsa_circ_59710 59617 RMVar_ID_59617 Human_SNP_ID_514152876 m1A Human chr12 - 104288967 104288967 104288967 CAAACACAACGGGCAGATCGGTTTCCGCGGCCAATTCCGAGAGCGTTCCTTCCAGGGCCCGACCG CAAACACAACGGGCAGATCGGTTTCCGCGGCCTATTCCGAGAGCGTTCCTTCCAGGGCCCGACCG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:104288878..104288968 26863196 MeRIP-seq:(Medium) rs756997829 Functional Loss SNV dbSNP153 33..33 33 - - - 59618 RMVar_ID_59618 Human_SNP_ID_514152884 m1A Human chr12 + 104288982 104288982 104288982 AGGAACGCTCTCGGAATTGGCCGCGGAAACCGATCTGCCCGTTGTGTTTGTGAAACAGAGAAAGA AGGAACGCTCTCGGAATTGGCCGCGGAAACCGGTCTGCCCGTTGTGTTTGTGAAACAGAGAAAGA A G TXNRD1 Ensembl:ENSG00000198431 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:104288883..104289085;chr12:104288895..104289066 26863196 MeRIP-seq:(Medium) rs1212274281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229495,Human_RBP_ID_408662,Human_RBP_ID_1463150,Human_RBP_ID_4246938,Human_RBP_ID_5554518,Human_RBP_ID_9366875,Human_RBP_ID_11786615,Human_RBP_ID_23532844,Human_RBP_ID_24543325,Human_RBP_ID_26323311,Human_RBP_ID_26411263 Human_Splice_Rec_1416834,Human_Splice_Rec_1416835,Human_Splice_Rec_1416864,Human_Splice_Rec_1416865,Human_Splice_Rec_1416904,Human_Splice_Rec_1416905,Human_Splice_Rec_1416910,Human_Splice_Rec_1416911,Human_Splice_Rec_1416960,Human_Splice_Rec_1416961,Human_Splice_Rec_1416986,Human_Splice_Rec_1416987,Human_Splice_Rec_1417012,Human_Splice_Rec_1417013,Human_Splice_Rec_1417038,Human_Splice_Rec_1417039,Human_Splice_Rec_1417046,Human_Splice_Rec_1417047,Human_Splice_Rec_1417076,Human_Splice_Rec_1417077,Human_Splice_Rec_1417084,Human_Splice_Rec_1417085,Human_Splice_Rec_1417116,Human_Splice_Rec_1417118,Human_Splice_Rec_1417119,Human_Splice_Rec_1417130,Human_Splice_Rec_1417131,Human_Splice_Rec_1417136,Human_Splice_Rec_1417137,Human_Splice_Rec_1417161,Human_Splice_Rec_1417187 RMVar_hsa_circ_59710,RMVar_hsa_circ_159394,RMVar_hsa_circ_282578,RMVar_hsa_circ_302954,RMVar_hsa_circ_361855,RMVar_hsa_circ_363515,RMVar_hsa_circ_375176,RMVar_hsa_circ_360816,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_62185,RMVar_hsa_circ_159395,RMVar_hsa_circ_159396 59619 RMVar_ID_59619 Human_SNP_ID_514155829 m1A Human chr12 + 104300224 104300224 104300224 GAATGCTTGGAATTAACCTAAACTCCTAGAAAAGGAACTGAAAATATAGGAGAAAAGGGTGAAGA GAATGCTTGGAATTAACCTAAACTCCTAGAAAGGGAACTGAAAATATAGGAGAAAAGGGTGAAGA A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:104300220..104300337 26863196 MeRIP-seq:(Medium) rs1240694737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282578,RMVar_hsa_circ_361855,RMVar_hsa_circ_375176,RMVar_hsa_circ_360816,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_62185,RMVar_hsa_circ_159395,RMVar_hsa_circ_159396 59620 RMVar_ID_59620 Human_SNP_ID_514156757 m1A Human chr12 + 104303808 104303808 104303808 CCACACGCTGGGAGGGCCGTTACCTCAGAGATACCCGTGGCCGGCATGTTGGTTGAAAAAGCTTC CCACACGCTGGGAGGGCCGTTACCTCAGAGATGCCCGTGGCCGGCATGTTGGTTGAAAAAGCTTC A G EID3,TXNRD1 Ensembl:ENSG00000255150,Ensembl:ENSG00000198431 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:104303807..104303985 26863196 MeRIP-seq:(Medium) rs572280235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11787200,Human_RBP_ID_22710089 RMVar_hsa_circ_282578,RMVar_hsa_circ_361855,RMVar_hsa_circ_375176,RMVar_hsa_circ_360816,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_62185,RMVar_hsa_circ_159395,RMVar_hsa_circ_159396 59621 RMVar_ID_59621 Human_SNP_ID_514159438 m1A Human chr12 + 104313196 104313196 104313196 AAAAATCATGGATTTTTAACAGCCCATTTCCAATCTGTCATGTTAACCTTTCCAACTCACTTTAA AAAAATCATGGATTTTTAACAGCCCATTTCCAGTCTGTCATGTTAACCTTTCCAACTCACTTTAA A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:104313193..104313370 26863196 MeRIP-seq:(Medium) rs561020634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159399,RMVar_hsa_circ_282578,RMVar_hsa_circ_361855,RMVar_hsa_circ_375176,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_62185,RMVar_hsa_circ_159395,RMVar_hsa_circ_159396,RMVar_hsa_circ_303450,RMVar_hsa_circ_338076,RMVar_hsa_circ_347810,RMVar_hsa_circ_363158,RMVar_hsa_circ_348452,RMVar_hsa_circ_342725,RMVar_hsa_circ_279402,RMVar_hsa_circ_286706,RMVar_hsa_circ_159397,RMVar_hsa_circ_159398 59622 RMVar_ID_59622 Human_SNP_ID_514160144 m1A Human chr12 - 104315865 104315865 104315865 CCTGTCTCCTCGACTTTCCATCCATAATTTCGAGAGTCTTGCAGGGCTTGTCCTAACAAAGCTGC CCTGTCTCCTCGACTTTCCATCCATAATTTCGGGAGTCTTGCAGGGCTTGTCCTAACAAAGCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:104315783..104315942 26863196 MeRIP-seq:(Medium) rs1197745685 Functional Loss SNV dbSNP153 33..33 33 - - - 59623 RMVar_ID_59623 Human_SNP_ID_514163362 m1A Human chr12 + 104327467 104327464 104327468 TCCCTGAAAAAACGGAAGATTTTGTTCTCCTTAATTAATAATGGTAATTAATGATGATTTTTAAC TCCCTGAAAAAACGGAAGATTTTGTTCTCC____TTAATAATGGTAATTAATGATGATTTTTAAC CTTAA C TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:104327464..104327718 26863196 MeRIP-seq:(Medium) rs1373225622 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_1801,RMVar_hsa_circ_361855,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_159396,RMVar_hsa_circ_338076,RMVar_hsa_circ_363158,RMVar_hsa_circ_279402,RMVar_hsa_circ_286706,RMVar_hsa_circ_12512,RMVar_hsa_circ_159397,RMVar_hsa_circ_159398,RMVar_hsa_circ_47757,RMVar_hsa_circ_353210,RMVar_hsa_circ_342619,RMVar_hsa_circ_352554,RMVar_hsa_circ_323939,RMVar_hsa_circ_48515,RMVar_hsa_circ_15551,RMVar_hsa_circ_159404,RMVar_hsa_circ_35280,RMVar_hsa_circ_275981,RMVar_hsa_circ_276176,RMVar_hsa_circ_62582,RMVar_hsa_circ_159405,RMVar_hsa_circ_159406,RMVar_hsa_circ_159407,RMVar_hsa_circ_344446,RMVar_hsa_circ_361014,RMVar_hsa_circ_80885 59624 RMVar_ID_59624 Human_SNP_ID_514163363 m1A Human chr12 + 104327467 104327467 104327467 TCCCTGAAAAAACGGAAGATTTTGTTCTCCTTAATTAATAATGGTAATTAATGATGATTTTTAAC TCCCTGAAAAAACGGAAGATTTTGTTCTCCTTGATTAATAATGGTAATTAATGATGATTTTTAAC A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:104327464..104327718 26863196 MeRIP-seq:(Medium) rs149045251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1801,RMVar_hsa_circ_361855,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_159396,RMVar_hsa_circ_338076,RMVar_hsa_circ_363158,RMVar_hsa_circ_279402,RMVar_hsa_circ_286706,RMVar_hsa_circ_12512,RMVar_hsa_circ_159397,RMVar_hsa_circ_159398,RMVar_hsa_circ_47757,RMVar_hsa_circ_353210,RMVar_hsa_circ_342619,RMVar_hsa_circ_352554,RMVar_hsa_circ_323939,RMVar_hsa_circ_48515,RMVar_hsa_circ_15551,RMVar_hsa_circ_159404,RMVar_hsa_circ_35280,RMVar_hsa_circ_275981,RMVar_hsa_circ_276176,RMVar_hsa_circ_62582,RMVar_hsa_circ_159405,RMVar_hsa_circ_159406,RMVar_hsa_circ_159407,RMVar_hsa_circ_344446,RMVar_hsa_circ_361014,RMVar_hsa_circ_80885 59625 RMVar_ID_59625 Human_SNP_ID_514168783 m1A Human chr12 + 104349878 104349878 104349878 ACCCATGCATCTGCCTGGCATTTAGGCAGCAGAGCCCCTGACCGTCCCCCACAGGGCTCTGCCTC ACCCATGCATCTGCCTGGCATTTAGGCAGCAGTGCCCCTGACCGTCCCCCACAGGGCTCTGCCTC A T TXNRD1 Ensembl:ENSG00000198431 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr12:104349827..104349941;chr12:104349651..104350206 26863196,32194978 MeRIP-seq:(Medium) rs574804673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36116,Human_RBP_ID_6123177,Human_RBP_ID_17235784,Human_RBP_ID_17351476,Human_RBP_ID_17467596,Human_RBP_ID_17683193,Human_RBP_ID_17807541,Human_RBP_ID_18254369,Human_RBP_ID_19701635,Human_RBP_ID_26411317 Human_miRNA_ID_2395588,Human_miRNA_ID_3069377 RMVar_hsa_circ_159407,RMVar_hsa_circ_80885 59626 RMVar_ID_59626 Human_SNP_ID_514184915 m1A Human chr12 - 104416539 104416539 104416539 CTCATTTTTGGATATTTTCTGTACCATCCCCTATGCTCCATTCGCTCTGCTACCCTGGCCTTCAC CTCATTTTTGGATATTTTCTGTACCATCCCCTGTGCTCCATTCGCTCTGCTACCCTGGCCTTCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:104416376..104416596 26863196 MeRIP-seq:(Medium) rs530537538 Functional Loss SNV dbSNP153 33..33 33 - - - 59627 RMVar_ID_59627 Human_SNP_ID_514317028 m1A Human chr12 + 104986408 104986408 104986408 GGCTAGCCCGAGTTGTTCGTCGCCCACCCGGGATTCCTCAGGAGTCCCAGTGTCCAAGGAGCTGC GGCTAGCCCGAGTTGTTCGTCGCCCACCCGGGTTTCCTCAGGAGTCCCAGTGTCCAAGGAGCTGC A T C12orf45 Ensembl:ENSG00000151131 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:104986357..104986429 26863196 MeRIP-seq:(Medium) rs201369478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_408800,Human_RBP_ID_4246941,Human_RBP_ID_22437380,Human_RBP_ID_23207820 Human_Splice_Rec_1417291,Human_Splice_Rec_1417297,Human_Splice_Rec_1417305,Human_Splice_Rec_1417313,Human_Splice_Rec_1417323 59628 RMVar_ID_59628 Human_SNP_ID_514346708 m1A Human chr12 + 105107788 105107788 105107788 CCGCACGGGCTGGTTGGGGCTGTGTCTGTGGGAGGCGCCGGGGTGATGGCGGTGGAGACTCTGTC CCGCACGGGCTGGTTGGGGCTGTGTCTGTGGGGGGCGCCGGGGTGATGGCGGTGGAGACTCTGTC A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:105107726..105111196 26863196 MeRIP-seq:(Medium) rs562615723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229982,Human_RBP_ID_754769,Human_RBP_ID_4246942,Human_RBP_ID_5314647,Human_RBP_ID_9352767,Human_RBP_ID_18417325,Human_RBP_ID_18433423,Human_RBP_ID_23533488 Human_Splice_Rec_1417517,Human_Splice_Rec_1417565,Human_Splice_Rec_1417629,Human_Splice_Rec_1417693,Human_Splice_Rec_1417757 59629 RMVar_ID_59629 Human_SNP_ID_514346723 m1A Human chr12 + 105107811 105107811 105107811 GTCTGTGGGAGGCGCCGGGGTGATGGCGGTGGAGACTCTGTCCCCGGACTGGGAGTTTGACCGCG GTCTGTGGGAGGCGCCGGGGTGATGGCGGTGGCGACTCTGTCCCCGGACTGGGAGTTTGACCGCG A C WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:105107761..105111151 26863196 MeRIP-seq:(Medium) rs929742452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229982,Human_RBP_ID_754769,Human_RBP_ID_4246942,Human_RBP_ID_5314647,Human_RBP_ID_9352767,Human_RBP_ID_18417325 Human_Splice_Rec_1417517,Human_Splice_Rec_1417565,Human_Splice_Rec_1417629,Human_Splice_Rec_1417693,Human_Splice_Rec_1417757 59630 RMVar_ID_59630 Human_SNP_ID_514346724 m1A Human chr12 + 105107811 105107811 105107811 GTCTGTGGGAGGCGCCGGGGTGATGGCGGTGGAGACTCTGTCCCCGGACTGGGAGTTTGACCGCG GTCTGTGGGAGGCGCCGGGGTGATGGCGGTGGGGACTCTGTCCCCGGACTGGGAGTTTGACCGCG A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:105107761..105111151 26863196 MeRIP-seq:(Medium) rs929742452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229982,Human_RBP_ID_754769,Human_RBP_ID_4246942,Human_RBP_ID_5314647,Human_RBP_ID_9352767,Human_RBP_ID_18417325 Human_Splice_Rec_1417517,Human_Splice_Rec_1417565,Human_Splice_Rec_1417629,Human_Splice_Rec_1417693,Human_Splice_Rec_1417757 59631 RMVar_ID_59631 Human_SNP_ID_514347602 m1A Human chr12 - 105111074 105111074 105111074 ACAGTATGTGATAAGTGCAAGTAATGAATTGCAGGACATTTACTTCAAATAACCTCAAAAGTCAC ACAGTATGTGATAAGTGCAAGTAATGAATTGCTGGACATTTACTTCAAATAACCTCAAAAGTCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:105111072..105111155 26863196 MeRIP-seq:(Medium) rs776428689 Functional Loss SNV dbSNP153 33..33 33 - - - 59632 RMVar_ID_59632 Human_SNP_ID_514358826 m1A Human chr12 + 105155280 105155280 105155280 GGCTGGGCAGTGCTAGTCAGTGATGTTCAGGGAAAACAGGAGGTGACATTTGAGCAGGGACCTAA GGCTGGGCAGTGCTAGTCAGTGATGTTCAGGGGAAACAGGAGGTGACATTTGAGCAGGGACCTAA A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:105155194..105155349 26863196 MeRIP-seq:(Medium) rs1303562985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752707,Human_RBP_ID_811561 RMVar_hsa_circ_37136,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_339409,RMVar_hsa_circ_108083,RMVar_hsa_circ_159468,RMVar_hsa_circ_57806,RMVar_hsa_circ_16195,RMVar_hsa_circ_14939,RMVar_hsa_circ_7055,RMVar_hsa_circ_300722,RMVar_hsa_circ_367358,RMVar_hsa_circ_299786,RMVar_hsa_circ_159474,RMVar_hsa_circ_159475,RMVar_hsa_circ_289891,RMVar_hsa_circ_296674,RMVar_hsa_circ_159476 59633 RMVar_ID_59633 Human_SNP_ID_514379754 m1A Human chr12 + 105236046 105236046 105236046 GTGCGGCGCGGCTCAGCCGAGGGCTGGGTTGGAAGGACAGAGGGCAGGAGACGCGGCGGCCGAGA GTGCGGCGCGGCTCAGCCGAGGGCTGGGTTGGGAGGACAGAGGGCAGGAGACGCGGCGGCCGAGA A G C12orf75 Ensembl:ENSG00000235162 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:105235995..105236148 26863196 MeRIP-seq:(Medium) rs1480295195 Functional Loss SNV dbSNP153 33..33 33 - - - 59634 RMVar_ID_59634 Human_SNP_ID_514379759 m1A Human chr12 + 105236064 105236064 105236064 GAGGGCTGGGTTGGAAGGACAGAGGGCAGGAGACGCGGCGGCCGAGAGCACTCCCCGGCTCTGGG GAGGGCTGGGTTGGAAGGACAGAGGGCAGGAGGCGCGGCGGCCGAGAGCACTCCCCGGCTCTGGG A G C12orf75 Ensembl:ENSG00000235162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:105235907..105236089 26863196 MeRIP-seq:(Medium) rs1174679647 Functional Loss SNV dbSNP153 33..33 33 - - - 59635 RMVar_ID_59635 Human_SNP_ID_514402840 m1A Human chr12 - 105330798 105330798 105330798 ACCCAGACGAAGGGCGGCGCACCCCGAGCGGGAGGCTGACGGGGCCGCGAGGGGCCAGGAACCGA ACCCAGACGAAGGGCGGCGCACCCCGAGCGGGTGGCTGACGGGGCCGCGAGGGGCCAGGAACCGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr12:105330697..105353520;chr12:105330723..105330824 26863410 MeRIP-seq:(Medium) rs1454346646 Functional Loss SNV dbSNP153 33..33 33 - - - 59636 RMVar_ID_59636 Human_SNP_ID_514408546 m1A Human chr12 + 105354693 105354693 105354693 ATATTGAGGGCCTTGCTGTGGTTAGAAATCATATATTCCCATTGGTAGCCATGATGAGATTTTCC ATATTGAGGGCCTTGCTGTGGTTAGAAATCATGTATTCCCATTGGTAGCCATGATGAGATTTTCC A G C12orf75 Ensembl:ENSG00000235162 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:105354691..105354836 26863196 MeRIP-seq:(Medium) rs917360833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83909,RMVar_hsa_circ_105214,RMVar_hsa_circ_159498,RMVar_hsa_circ_159499 59637 RMVar_ID_59637 Human_SNP_ID_514411917 m1A Human chr12 - 105367511 105367511 105367511 AATATATAGAATTATTTAGAAAAATATACAGCACCTCTTGATTCTTGAGTCATGATGTTATTTTC AATATATAGAATTATTTAGAAAAATATACAGCTCCTCTTGATTCTTGAGTCATGATGTTATTTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:105366688..105370688 32194978 MeRIP-seq:(Medium) rs775242075 Functional Loss SNV dbSNP153 33..33 33 - - - 59638 RMVar_ID_59638 Human_SNP_ID_514577854 m1A Human chr12 - 106079249 106079249 106079249 GCAAGCACAGGAACACAGCATGGAGACTAGAAAAGGAAAGTAATGCTTACTGAGCCCCTGCTAGA GCAAGCACAGGAACACAGCATGGAGACTAGAAGAGGAAAGTAATGCTTACTGAGCCCCTGCTAGA T C NUAK1 Ensembl:ENSG00000074590 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:106079247..106079389 26863196 MeRIP-seq:(Medium) rs117172173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89769,RMVar_hsa_circ_40699,RMVar_hsa_circ_159507,RMVar_hsa_circ_271874 59639 RMVar_ID_59639 Human_SNP_ID_514591228 m1A Human chr12 + 106138553 106138553 106138553 GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCAGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCCGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:106138506..106138638 26863196 MeRIP-seq:(Medium) rs751592845 Functional Loss SNV dbSNP153 33..33 33 - - - 59640 RMVar_ID_59640 Human_SNP_ID_514591229 m1A Human chr12 + 106138553 106138553 106138553 GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCAGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCGGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:106138506..106138638 26863196 MeRIP-seq:(Medium) rs751592845 Functional Loss SNV dbSNP153 33..33 33 - - - 59641 RMVar_ID_59641 Human_SNP_ID_514591321 m1A Human chr12 + 106138767 106138767 106138767 CGCTGTACGCTCAAGGTCGCCCCCGCAGCATCAGGGAGGCGGCCCGATACCGCTCGGACTGCGGC CGCTGTACGCTCAAGGTCGCCCCCGCAGCATCCGGGAGGCGGCCCGATACCGCTCGGACTGCGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:106138716..106138961 26863196 MeRIP-seq:(Medium) rs1365469628 Functional Loss SNV dbSNP153 33..33 33 - - - 59642 RMVar_ID_59642 Human_SNP_ID_514591485 m1A Human chr12 + 106139190 106139190 106139190 TGTCGCGACTCGCCCTTTGTGCGGCGCGGCGTAGGCCACGGCGGCGGCGGCGGCGGCGGCCAGGA TGTCGCGACTCGCCCTTTGTGCGGCGCGGCGTGGGCCACGGCGGCGGCGGCGGCGGCGGCCAGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:106139149..106139252;chr12:106139160..106139307 26863196 MeRIP-seq:(Medium) rs989794937 Functional Loss SNV dbSNP153 33..33 33 - - - 59643 RMVar_ID_59643 Human_SNP_ID_514615727 m1A Human chr12 - 106239301 106239301 106239301 GGAATCACTCCAGAAGGTGCAGGAGCAGGTGCACACGCTGCTCAGTCAGGACCAAGCCCAGGCCG GGAATCACTCCAGAAGGTGCAGGAGCAGGTGCGCACGCTGCTCAGTCAGGACCAAGCCCAGGCCG T C CKAP4 Ensembl:ENSG00000136026 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:106239251..106239920 32194978 MeRIP-seq:(Medium) rs766741048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22756952,Human_RBP_ID_27418013 Human_miRNA_ID_245356,Human_miRNA_ID_247862 59644 RMVar_ID_59644 Human_SNP_ID_514615748 m1A Human chr12 + 106239357 106239357 106239357 AGTGATTCCACGGTGCTGGGGAGCTCGCCCACACTCCTCTTCAGCTCCTCCACGTCACCGTAGAG AGTGATTCCACGGTGCTGGGGAGCTCGCCCACCCTCCTCTTCAGCTCCTCCACGTCACCGTAGAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:106239351..106239375 26863196 MeRIP-seq:(Medium) rs745610546 Functional Loss SNV dbSNP153 33..33 33 - - - 59645 RMVar_ID_59645 Human_SNP_ID_514615791 m1A Human chr12 - 106239439 106239439 106239439 CCTGGAAGGCCTCGGGTCCTCAGAGGCAGACCAGGATGGCCTGGCCAGCACGGTGAGGAGCCTGG CCTGGAAGGCCTCGGGTCCTCAGAGGCAGACCGGGATGGCCTGGCCAGCACGGTGAGGAGCCTGG T C CKAP4 Ensembl:ENSG00000136026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:106239388..106239519 26863196 MeRIP-seq:(Medium) rs143082078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18469341,Human_RBP_ID_22436665,Human_RBP_ID_22756954 59646 RMVar_ID_59646 Human_SNP_ID_514616059 m1A Human chr12 + 106240070 106240063 106240070 CTCCTTCTGGCTCCTCTTCTGGACTTCTGTGAAGATGGCGATGTTGTCGTTGATGGATTTGGTGA CTCCTTCTGGCTCCTCTTCTGGACTT_______GATGGCGATGTTGTCGTTGATGGATTTGGTGA TCTGTGAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:106239797..106240161 26863196 MeRIP-seq:(Medium) rs1177979508 Functional Loss DEL dbSNP153 27..33 33 - - - 59647 RMVar_ID_59647 Human_SNP_ID_514616162 m1A Human chr12 - 106240351 106240351 106240351 TTCTCAGCAATTAACGTCTGGATTTTGATTACAGGTGCAGTCTTTGCAAGCCACATTTGGAACTT TTCTCAGCAATTAACGTCTGGATTTTGATTACGGGTGCAGTCTTTGCAAGCCACATTTGGAACTT T C CKAP4 Ensembl:ENSG00000136026 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:106240317..106247525 32194978 MeRIP-seq:(Medium) rs1302415864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2300692 59648 RMVar_ID_59648 Human_SNP_ID_514617889 m1A Human chr12 - 106247348 106247348 106247348 GTCGAGCAGAAGGTGGGTACCCCCGGCCCCGCAACTGTCCCCATCGACTGCGGCCTCCGGACCCA GTCGAGCAGAAGGTGGGTACCCCCGGCCCCGCGACTGTCCCCATCGACTGCGGCCTCCGGACCCA T C CKAP4 Ensembl:ENSG00000136026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:106247347..106247450 26863196 MeRIP-seq:(Medium) rs1168278392 Functional Loss SNV dbSNP153 33..33 33 - - - 59649 RMVar_ID_59649 Human_SNP_ID_514617907 m1A Human chr12 + 106247389 106247389 106247389 GGGGGTACCCACCTTCTGCTCGACGCCCTGCAAGCCCTGGCCCAGCTCCTCCCTCTGCCGGGAGA GGGGGTACCCACCTTCTGCTCGACGCCCTGCATGCCCTGGCCCAGCTCCTCCCTCTGCCGGGAGA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:106247376..106247400 26863196 MeRIP-seq:(Medium) rs766454750 Functional Loss SNV dbSNP153 33..33 33 - - - 59650 RMVar_ID_59650 Human_SNP_ID_514618152 m1A Human chr12 - 106247730 106247730 106247730 TGACGTGGCGAAGAAGCCGCCGCCGGCGCCGCAGCAGCCGCCGCCGCCGCCCGCGCCGCACCCGC TGACGTGGCGAAGAAGCCGCCGCCGGCGCCGCCGCAGCCGCCGCCGCCGCCCGCGCCGCACCCGC T G CKAP4 Ensembl:ENSG00000136026 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:106247680..106248000 26863196 MeRIP-seq:(Medium) rs1254793984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755713,Human_RBP_ID_4246280,Human_RBP_ID_18469237,Human_RBP_ID_22436673 59651 RMVar_ID_59651 Human_SNP_ID_514618206 m1A Human chr12 - 106247883 106247883 106247883 CCCGGGCCGCGCGCCGCGCTCGCTCGCCTCCCAGCCCGCGGCCCGAGCCGCCGCCGCGCCCGCCA CCCGGGCCGCGCGCCGCGCTCGCTCGCCTCCCGGCCCGCGGCCCGAGCCGCCGCCGCGCCCGCCA T C CKAP4 Ensembl:ENSG00000136026 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr12:106247626..106248010;chr12:106247651..106248025 26863196 MeRIP-seq:(Medium) rs1229376640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229981,Human_RBP_ID_4198105,Human_RBP_ID_22436674 59652 RMVar_ID_59652 Human_SNP_ID_514644915 m1A Human chr12 + 106357877 106357877 106357877 AGGTTCTATCTGTTTCTTCCTCCTTCGTGAGCAGCATGGACGTGCTAGCGGAGGAGTTTGGGAAC AGGTTCTATCTGTTTCTTCCTCCTTCGTGAGCGGCATGGACGTGCTAGCGGAGGAGTTTGGGAAC A G POLR3B Ensembl:ENSG00000013503 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:106357826..106357924 26863196 MeRIP-seq:(Medium) rs1271343590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247760,Human_RBP_ID_18616372 Human_Splice_Rec_1418289 59653 RMVar_ID_59653 Human_SNP_ID_514644916 m1A Human chr12 + 106357877 106357877 106357877 AGGTTCTATCTGTTTCTTCCTCCTTCGTGAGCAGCATGGACGTGCTAGCGGAGGAGTTTGGGAAC AGGTTCTATCTGTTTCTTCCTCCTTCGTGAGCTGCATGGACGTGCTAGCGGAGGAGTTTGGGAAC A T POLR3B Ensembl:ENSG00000013503 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:106357826..106357924 26863196 MeRIP-seq:(Medium) rs1271343590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247760,Human_RBP_ID_18616372 Human_Splice_Rec_1418289 59654 RMVar_ID_59654 Human_SNP_ID_514741272 m1A Human chr12 - 106774656 106774645 106774657 TAAACGCCTCGCGCCCCCGCTCGCTCCTTCCCAGCTTCCTTCCTTCCCTCTTTCCCTCCCTCCGT TAAACGCCTCGCGCCCCCGCTCGCTCCTTCC____________TTCCCTCTTTCCCTCCCTCCGT AGGAAGGAAGCTG A AC079385.1 Ensembl:ENSG00000257545 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:106507791..106774850;chr12:106507791..106774819 26863196 MeRIP-seq:(Medium) rs557717847 Functional Loss DEL dbSNP153 32..43 33 - - - 59655 RMVar_ID_59655 Human_SNP_ID_514783245 m1A Human chr12 - 106956001 106956001 106956001 CCGGGCGGAGTGAGCGGGCCGGCGCAGAGGAGAGCTGAGGCGGCCTGGGCGGCAGCGGCGGCCGG CCGGGCGGAGTGAGCGGGCCGGCGCAGAGGAGCGCTGAGGCGGCCTGGGCGGCAGCGGCGGCCGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:106955951..106956075 32194978 MeRIP-seq:(Medium) rs1002680141 Functional Loss SNV dbSNP153 33..33 33 - - - 59656 RMVar_ID_59656 Human_SNP_ID_514785862 m1A Human chr12 - 106967103 106967103 106967103 TTTTATCTGTCTGATTCATGATCTCCTAAAAAAAAAACATACAAACACATTTCATTTTAACCTCA TTTTATCTGTCTGATTCATGATCTCCTAAAAAGAAAACATACAAACACATTTCATTTTAACCTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:106967101..106967150 26863196 MeRIP-seq:(Medium) rs1566225018 Functional Loss SNV dbSNP153 33..33 33 - - - 59657 RMVar_ID_59657 Human_SNP_ID_514786769 m1A Human chr12 - 106971106 106971106 106971106 CCTGGCTGCTGCTGTGGGTGATCTTTCATTGAACCTAATGAGAGAAAATATCATGAGACAATCAA CCTGGCTGCTGCTGTGGGTGATCTTTCATTGAGCCTAATGAGAGAAAATATCATGAGACAATCAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:106971101..106971300 32194978 MeRIP-seq:(Medium) rs765374011 Functional Loss SNV dbSNP153 33..33 33 - - - 59658 RMVar_ID_59658 Human_SNP_ID_514790444 m1A Human chr12 + 106986967 106986967 106986967 ACACGCCCAGGAGCAGAGGAAGGGGGCGACTCACCCGTCGGCGTCAGCTCCAAGCAAGGCACAGG ACACGCCCAGGAGCAGAGGAAGGGGGCGACTCGCCCGTCGGCGTCAGCTCCAAGCAAGGCACAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:106986962..106987097 26863196 MeRIP-seq:(Medium) rs1218145002 Functional Loss SNV dbSNP153 33..33 33 - - - 59659 RMVar_ID_59659 Human_SNP_ID_514790476 m1A Human chr12 + 106987069 106987069 106987069 CCGGCCAGCCTCCCCACAGTCCGCAGTCCCCGAGGCCTGGAGCCGGGATTTCGGTCCTCGGTCTC CCGGCCAGCCTCCCCACAGTCCGCAGTCCCCGCGGCCTGGAGCCGGGATTTCGGTCCTCGGTCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:106986917..106987116;chr12:106986919..106987106 26863196 MeRIP-seq:(Medium) rs761159513 Functional Loss SNV dbSNP153 33..33 33 - - - 59660 RMVar_ID_59660 Human_SNP_ID_514793174 m1A Human chr12 - 106998044 106998044 106998044 ACTTCTGAAGGTATTTGAAGAATTATTGCTTGATGCAGATTGGAGCATAAATGCTGGAAGTTGGA ACTTCTGAAGGTATTTGAAGAATTATTGCTTGGTGCAGATTGGAGCATAAATGCTGGAAGTTGGA T C CRY1 Ensembl:ENSG00000008405 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:106997959..106999742 32194978 MeRIP-seq:(Medium) rs1158429803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1785713,Human_RBP_ID_8364049,Human_RBP_ID_9344354,Human_RBP_ID_11793098,Human_RBP_ID_18616472,Human_RBP_ID_23534510,Human_RBP_ID_27807127 Human_Splice_Rec_1418878,Human_Splice_Rec_1418906 RMVar_hsa_circ_24537,RMVar_hsa_circ_367630,RMVar_hsa_circ_311693,RMVar_hsa_circ_2312,RMVar_hsa_circ_123435,RMVar_hsa_circ_337508,RMVar_hsa_circ_8656,RMVar_hsa_circ_332074,RMVar_hsa_circ_72175,RMVar_hsa_circ_159564,RMVar_hsa_circ_378517 59661 RMVar_ID_59661 Human_SNP_ID_514816277 m1A Human chr12 + 107093237 107093237 107093237 CCGCGCCCGCCGCAACCGCCTGGAGGCGACGCATAACTTCGAGGGCCTCGGACCTCCGGAGCCTG CCGCGCCCGCCGCAACCGCCTGGAGGCGACGCGTAACTTCGAGGGCCTCGGACCTCCGGAGCCTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:107092935..107093335 26863196 MeRIP-seq:(Medium) rs1443672726 Functional Loss SNV dbSNP153 33..33 33 - - - 59662 RMVar_ID_59662 Human_SNP_ID_514816308 m1A Human chr12 + 107093314 107093313 107093314 GAGCTCGAGCCGCCACGACGGCCCGAGCCGGCACGGACGGCCCCAGGAGATTCGTCACGGAAACC GAGCTCGAGCCGCCACGACGGCCCGAGCCGGC_CGGACGGCCCCAGGAGATTCGTCACGGAAACC CA C AC078929.1 Ensembl:ENSG00000257548 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:107093264..107093370 32194978 MeRIP-seq:(Medium) rs1292142165 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1418925 59663 RMVar_ID_59663 Human_SNP_ID_514816356 m1A Human chr12 + 107093504 107093484 107093504 CGGAGGCTAGAGGCGGTGGTCGAGGCCGCTGGACGGTTGCCGGCCGGTGACCGGTCCCGAGGCTG CGGAGGCTAGAGG____________________CGGTTGCCGGCCGGTGACCGGTCCCGAGGCTG GCGGTGGTCGAGGCCGCTGGA G AC078929.1 Ensembl:ENSG00000257548 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:107093414..107093531 26863196 MeRIP-seq:(Medium) rs1261803665 Functional Loss DEL dbSNP153 14..33 33 - - - 59664 RMVar_ID_59664 Human_SNP_ID_514816467 m1A Human chr12 - 107093751 107093751 107093751 CGGCACAGGAAAGGGGCAGAGGCAGTGAGTTCAGCGTGTGGACGAGGGTCAACAAGTTTGGGATC CGGCACAGGAAAGGGGCAGAGGCAGTGAGTTCGGCGTGTGGACGAGGGTCAACAAGTTTGGGATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:107093710..107093794 26863196 MeRIP-seq:(Medium) rs980695187 Functional Loss SNV dbSNP153 33..33 33 - - - 59665 RMVar_ID_59665 Human_SNP_ID_514859073 m1A Human chr12 + 107271762 107271762 107271762 GAAGATGAGGAAGGATTAGAAGATATTGATGAAGAAGGGGGTGAGGATGAAGGTGAAGAAGATGA GAAGATGAGGAAGGATTAGAAGATATTGATGAGGAAGGGGGTGAGGATGAAGGTGAAGAAGATGA A G SETP7 Ensembl:ENSG00000257444 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:107271716..107271807 26863196 MeRIP-seq:(Medium) rs73398509 Functional Loss SNV dbSNP153 33..33 33 - - - 59666 RMVar_ID_59666 Human_SNP_ID_514957939 m1A Human chr12 + 107685860 107685860 107685860 GGCAGCAGTGCGGTCGTGGTCCCTCCCTATGCAGCCTGGTTTCTAGCGTGACACGCCCTTGACTT GGCAGCAGTGCGGTCGTGGTCCCTCCCTATGCCGCCTGGTTTCTAGCGTGACACGCCCTTGACTT A C PWP1 Ensembl:ENSG00000136045 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:107685801..107685975 26863196 MeRIP-seq:(Medium) rs1205286082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753730,Human_RBP_ID_4246949,Human_RBP_ID_8787351,Human_RBP_ID_9279187,Human_RBP_ID_11793887,Human_RBP_ID_18616533,Human_RBP_ID_26321943,Human_RBP_ID_26900261 Human_miRNA_ID_2093367 RMVar_hsa_circ_94912,RMVar_hsa_circ_111878,RMVar_hsa_circ_159579,RMVar_hsa_circ_87674,RMVar_hsa_circ_159580,RMVar_hsa_circ_159578 59667 RMVar_ID_59667 Human_SNP_ID_514957976 m1A Human chr12 + 107685955 107685955 107685955 GTGCGTGGCCTGGGTCCGCTGCGGCGTGGCCAAAGAGACACCAGACAAGGTGAGGCCTGGTCGCT GTGCGTGGCCTGGGTCCGCTGCGGCGTGGCCACAGAGACACCAGACAAGGTGAGGCCTGGTCGCT A C PWP1 Ensembl:ENSG00000136045 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:107685801..107686099;chr12:107685801..107686020 26863196 MeRIP-seq:(Medium) rs747030058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811381,Human_RBP_ID_4246949,Human_RBP_ID_9279188,Human_RBP_ID_9365486 Human_Splice_Rec_1419075,Human_Splice_Rec_1419103,Human_Splice_Rec_1419115 Human_miRNA_ID_2675368,Human_miRNA_ID_2926119 RMVar_hsa_circ_94912,RMVar_hsa_circ_111878,RMVar_hsa_circ_159579,RMVar_hsa_circ_87674,RMVar_hsa_circ_159580,RMVar_hsa_circ_159578 59668 RMVar_ID_59668 Human_SNP_ID_514974185 m1A Human chr12 + 107749865 107749865 107749865 TTTGTGTTCTGGCTCCTACTTCTCCTCTCACCACATGACCCCTCTCTTCACCCTCATTTTATGCT TTTGTGTTCTGGCTCCTACTTCTCCTCTCACCGCATGACCCCTCTCTTCACCCTCATTTTATGCT A G AC007622.2 Ensembl:ENSG00000258136 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:107749611..107750054 26863196 MeRIP-seq:(Medium) rs1364054967 Functional Loss SNV dbSNP153 33..33 33 - - - 59669 RMVar_ID_59669 Human_SNP_ID_514977256 m1A Human chr12 - 107761075 107761075 107761075 GCCGGGAAGGGCCGGGCGGGACGGGAAACGTTAGGGCAGCGGCCCCCGGGGTGAGGGGGCCGAGC GCCGGGAAGGGCCGGGCGGGACGGGAAACGTTGGGGCAGCGGCCCCCGGGGTGAGGGGGCCGAGC T C PRDM4 Ensembl:ENSG00000110851 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:107760977..107761152 26863196 MeRIP-seq:(Medium) rs1254320526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753183,Human_RBP_ID_873831,Human_RBP_ID_4198724,Human_RBP_ID_8940723,Human_RBP_ID_18417327,Human_RBP_ID_26323322 RMVar_hsa_circ_94769,RMVar_hsa_circ_159592 59670 RMVar_ID_59670 Human_SNP_ID_515163832 m1A Human chr12 - 108517154 108517154 108517154 CGGCATGCTGCGCCCTGTCCGGTTTGCTCCTGAGCAGGTAGAGGCCTTTGAGCACAGCCAAGCAC CGGCATGCTGCGCCCTGTCCGGTTTGCTCCTGGGCAGGTAGAGGCCTTTGAGCACAGCCAAGCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:108517126..108517253 26863196 MeRIP-seq:(Medium) rs370547934 Functional Loss SNV dbSNP153 33..33 33 - - - 59671 RMVar_ID_59671 Human_SNP_ID_515166572 m1A Human chr12 + 108526451 108526451 108526451 TCTCCTTCTGCTTCGAAGGGGGCTCCACATCTACGGCAGCACATTTCCCAGCGGGCCCTGCTGCT TCTCCTTCTGCTTCGAAGGGGGCTCCACATCTGCGGCAGCACATTTCCCAGCGGGCCCTGCTGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:108526401..108526475 32194978 MeRIP-seq:(Medium) rs374066826 Functional Loss SNV dbSNP153 33..33 33 - - - 59672 RMVar_ID_59672 Human_SNP_ID_515167537 m1A Human chr12 - 108530192 108530192 108530192 AAAAAAGAAGAAAAAGATCAGAGGCCCAGAGAAGCGCGGAGCAGATGAGGATGATGAGAAAGAGT AAAAAAGAAGAAAAAGATCAGAGGCCCAGAGAGGCGCGGAGCAGATGAGGATGATGAGAAAGAGT T C SART3 Ensembl:ENSG00000075856 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:108526526..108530325 26863196 MeRIP-seq:(Medium) rs776107033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33368,Human_RBP_ID_228475,Human_RBP_ID_3942045,Human_RBP_ID_6126994,Human_RBP_ID_8229960,Human_RBP_ID_9365501,Human_RBP_ID_24543161,Human_RBP_ID_26321015,Human_RBP_ID_27807134 Human_Splice_Rec_1419495,Human_Splice_Rec_1419529,Human_Splice_Rec_1419565,Human_Splice_Rec_1419601,Human_Splice_Rec_1419635 RMVar_hsa_circ_44654,RMVar_hsa_circ_364089,RMVar_hsa_circ_364163,RMVar_hsa_circ_57993 59673 RMVar_ID_59673 Human_SNP_ID_515172218 m1A Human chr12 - 108549204 108549204 108549204 AACTTGTTTCTTTTCCTGTTAGTTGTCTATCAACGTCTATGACTACAACTGCCATGTGGACTTGA AACTTGTTTCTTTTCCTGTTAGTTGTCTATCAGCGTCTATGACTACAACTGCCATGTGGACTTGA T C SART3 Ensembl:ENSG00000075856 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:108547976..108554097 26863196 MeRIP-seq:(Medium) rs758154672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33380,Human_RBP_ID_873249,Human_RBP_ID_1463517,Human_RBP_ID_1785943,Human_RBP_ID_5350021,Human_RBP_ID_8364268,Human_RBP_ID_9365512,Human_RBP_ID_18410912,Human_RBP_ID_26321962 Human_Splice_Rec_1419468,Human_Splice_Rec_1419504,Human_Splice_Rec_1419538,Human_Splice_Rec_1419574,Human_Splice_Rec_1419610,Human_Splice_Rec_1419652,Human_Splice_Rec_1419702,Human_Splice_Rec_1419714,Human_Splice_Rec_1419720,Human_Splice_Rec_1419721 Human_miRNA_ID_2534682,Human_miRNA_ID_2536414 RMVar_hsa_circ_364163,RMVar_hsa_circ_22333,RMVar_hsa_circ_31176,RMVar_hsa_circ_60236,RMVar_hsa_circ_58297,RMVar_hsa_circ_72240,RMVar_hsa_circ_316581,RMVar_hsa_circ_32522,RMVar_hsa_circ_159605,RMVar_hsa_circ_285165,RMVar_hsa_circ_159606,RMVar_hsa_circ_334113 59674 RMVar_ID_59674 Human_SNP_ID_515175306 m1A Human chr12 - 108561052 108561052 108561052 GAGAGGAGGATGAGGTTAAGGCGGCTAGGACAAGGAGGAAGGTGTTATCGCGGGCTGTGGCCGCT GAGAGGAGGATGAGGTTAAGGCGGCTAGGACAGGGAGGAAGGTGTTATCGCGGGCTGTGGCCGCT T C SART3 Ensembl:ENSG00000075856 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:108560807..108561175 26863196 MeRIP-seq:(Medium) rs1565871444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4198970,Human_RBP_ID_9366895,Human_RBP_ID_18410913,Human_RBP_ID_18417328,Human_RBP_ID_26321964,Human_RBP_ID_27807141 59675 RMVar_ID_59675 Human_SNP_ID_515175931 m1A Human chr12 + 108562702 108562702 108562702 GCTGCTGCGGAGCCCCCGCCTGCCCGCCCGGGAGCTGTCGGCCCCGGCCCGACTCTATCACAAGA GCTGCTGCGGAGCCCCCGCCTGCCCGCCCGGGGGCTGTCGGCCCCGGCCCGACTCTATCACAAGA A G ISCU Ensembl:ENSG00000136003 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:108562651..108562750 32194978 MeRIP-seq:(Medium) rs567636479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_409547,Human_RBP_ID_755709,Human_RBP_ID_4198982,Human_RBP_ID_9322676,Human_RBP_ID_17808327 Human_Splice_Rec_1419733,Human_Splice_Rec_1419739,Human_Splice_Rec_1419747,Human_Splice_Rec_1419757,Human_Splice_Rec_1419767,Human_Splice_Rec_1419775,Human_Splice_Rec_1419787,Human_Splice_Rec_1419797,Human_Splice_Rec_1419803 59676 RMVar_ID_59676 Human_SNP_ID_515175951 m1A Human chr12 + 108562732 108562732 108562732 GGAGCTGTCGGCCCCGGCCCGACTCTATCACAAGAAGGTAGGGACAAAAGAGGGACGCGCGGAAT GGAGCTGTCGGCCCCGGCCCGACTCTATCACAGGAAGGTAGGGACAAAAGAGGGACGCGCGGAAT A G ISCU Ensembl:ENSG00000136003 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:108562658..108562799 26863196 MeRIP-seq:(Medium) rs537876845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246952,Human_RBP_ID_19056738 Human_Splice_Rec_1419733,Human_Splice_Rec_1419739,Human_Splice_Rec_1419747,Human_Splice_Rec_1419757,Human_Splice_Rec_1419767,Human_Splice_Rec_1419775,Human_Splice_Rec_1419787,Human_Splice_Rec_1419797,Human_Splice_Rec_1419803 59677 RMVar_ID_59677 Human_SNP_ID_515176438 m1A Human chr12 - 108564281 108564281 108564281 CCCACGTTTCTAGGATTTTCATAATGATCAACAACCTAAAATGAGAGGGTTAAGATAAATCATGT CCCACGTTTCTAGGATTTTCATAATGATCAACCACCTAAAATGAGAGGGTTAAGATAAATCATGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:108564276..108564350 32194978 MeRIP-seq:(Medium) rs747311255 Functional Loss SNV dbSNP153 33..33 33 - - - 59678 RMVar_ID_59678 Human_SNP_ID_515177189 m1A Human chr12 + 108567260 108567260 108567260 CAAGGAGCTCTGCCTTCCTCCCGTGAAACTGCACTGCTCCAGTAAGTCTCTGCTCTCCATACCAG CAAGGAGCTCTGCCTTCCTCCCGTGAAACTGCTCTGCTCCAGTAAGTCTCTGCTCTCCATACCAG A T ISCU Ensembl:ENSG00000136003 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:108565351..108567290 32194978 MeRIP-seq:(Medium) rs926473212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_409560,Human_RBP_ID_19059034 Human_Splice_Rec_1419730,Human_Splice_Rec_1419731,Human_Splice_Rec_1419738,Human_Splice_Rec_1419744,Human_Splice_Rec_1419745,Human_Splice_Rec_1419752,Human_Splice_Rec_1419753,Human_Splice_Rec_1419762,Human_Splice_Rec_1419763,Human_Splice_Rec_1419772,Human_Splice_Rec_1419773,Human_Splice_Rec_1419782,Human_Splice_Rec_1419783,Human_Splice_Rec_1419794,Human_Splice_Rec_1419795,Human_Splice_Rec_1419802,Human_Splice_Rec_1419808,Human_Splice_Rec_1419810 59679 RMVar_ID_59679 Human_SNP_ID_515177617 m1A Human chr12 + 108568932 108568932 108568932 AGGCAGAGAAGAAATGAGCCCTCCCTCGGCGAAGCCTCCAGCAGGCCACACCAGCTGTTTCCCAC AGGCAGAGAAGAAATGAGCCCTCCCTCGGCGAGGCCTCCAGCAGGCCACACCAGCTGTTTCCCAC A G ISCU Ensembl:ENSG00000136003 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:108568883..108568990 26863196 MeRIP-seq:(Medium) rs772428040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_409567,Human_RBP_ID_875030,Human_RBP_ID_26806009 59680 RMVar_ID_59680 Human_SNP_ID_515197340 m1A Human chr12 - 108646093 108646093 108646093 AGAATGATAGAGAGTGAAGCAGAAACAGGAGCACAGACCTCTGCTGTAGCTTTAATGCATACAAA AGAATGATAGAGAGTGAAGCAGAAACAGGAGCTCAGACCTCTGCTGTAGCTTTAATGCATACAAA T A CORO1C Ensembl:ENSG00000110880 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2111211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1785964,Human_RBP_ID_6127247,Human_RBP_ID_11796778,Human_RBP_ID_17830524,Human_RBP_ID_22382377,Human_RBP_ID_23155434,Human_RBP_ID_23535262,Human_RBP_ID_26411591 Human_miRNA_ID_623897,Human_miRNA_ID_2273092 GWAS_ID_6941 RMVar_hsa_circ_159609,RMVar_hsa_circ_101388,RMVar_hsa_circ_126274,RMVar_hsa_circ_159610 59681 RMVar_ID_59681 Human_SNP_ID_515197341 m1A Human chr12 - 108646093 108646093 108646093 AGAATGATAGAGAGTGAAGCAGAAACAGGAGCACAGACCTCTGCTGTAGCTTTAATGCATACAAA AGAATGATAGAGAGTGAAGCAGAAACAGGAGCGCAGACCTCTGCTGTAGCTTTAATGCATACAAA T C CORO1C Ensembl:ENSG00000110880 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2111211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1785964,Human_RBP_ID_6127247,Human_RBP_ID_11796778,Human_RBP_ID_17830524,Human_RBP_ID_22382377,Human_RBP_ID_23155434,Human_RBP_ID_23535262,Human_RBP_ID_26411591 Human_miRNA_ID_623897,Human_miRNA_ID_2273092 GWAS_ID_6941 RMVar_hsa_circ_159609,RMVar_hsa_circ_101388,RMVar_hsa_circ_126274,RMVar_hsa_circ_159610 59682 RMVar_ID_59682 Human_SNP_ID_515197622 m1A Human chr12 - 108647452 108647452 108647452 CAAATCTATAAAAGACACAATCTGCAATCAAGATGAGCGTATTTCCAAGTTAGAACAGCAGATGG CAAATCTATAAAAGACACAATCTGCAATCAAGTTGAGCGTATTTCCAAGTTAGAACAGCAGATGG T A CORO1C Ensembl:ENSG00000110880 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:108647401..108647502 32194978 MeRIP-seq:(Medium) rs755094723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33781,Human_RBP_ID_409661,Human_RBP_ID_1785977,Human_RBP_ID_6127303,Human_RBP_ID_11796821,Human_RBP_ID_23535298 Human_Splice_Rec_1419864,Human_Splice_Rec_1419884,Human_Splice_Rec_1419904,Human_Splice_Rec_1419910,Human_Splice_Rec_1419911,Human_Splice_Rec_1419920,Human_Splice_Rec_1419938,Human_Splice_Rec_1419954,Human_Splice_Rec_1419974 Human_miRNA_ID_2909284 RMVar_hsa_circ_159609,RMVar_hsa_circ_101388,RMVar_hsa_circ_126274,RMVar_hsa_circ_159610,RMVar_hsa_circ_346942 59683 RMVar_ID_59683 Human_SNP_ID_515216599 m1A Human chr12 + 108730244 108730244 108730244 AGCAAGCACTTTAGACACCACAAAACAAGGGCAGCCTACATTACGGCCAAATATAGGATGTGTTT AGCAAGCACTTTAGACACCACAAAACAAGGGCTGCCTACATTACGGCCAAATATAGGATGTGTTT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:108730240..108730548 32194978 MeRIP-seq:(Medium) rs1028422529 Functional Loss SNV dbSNP153 33..33 33 - - - 59684 RMVar_ID_59684 Human_SNP_ID_515216698 m1A Human chr12 - 108730578 108730578 108730578 AATAGCGGGGCAGCTGGCGAGGGACGCAGTAAAAAGGAGCGAGGTGCAGGTGGGGCCCCGCTGCG AATAGCGGGGCAGCTGGCGAGGGACGCAGTAAGAAGGAGCGAGGTGCAGGTGGGGCCCCGCTGCG T C CORO1C Ensembl:ENSG00000110880 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:108730576..108730691 26863196 MeRIP-seq:(Medium) rs970759076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418449,Human_RBP_ID_5314651,Human_RBP_ID_8070355,Human_RBP_ID_17186476,Human_RBP_ID_18479077 Human_Splice_Rec_1420031 RMVar_hsa_circ_98336,RMVar_hsa_circ_159621,RMVar_hsa_circ_110657,RMVar_hsa_circ_159622 59685 RMVar_ID_59685 Human_SNP_ID_515216936 m1A Human chr12 + 108731419 108731419 108731419 GACTCGCTCTCAGGCTGCCCCCGCCGGGCGCGAGCCGCTCACCCGGGCCGAGGTGCCTGAGGCGC GACTCGCTCTCAGGCTGCCCCCGCCGGGCGCGCGCCGCTCACCCGGGCCGAGGTGCCTGAGGCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:108731402..108731500 26863410 MeRIP-seq:(Medium) rs11114043 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6942,GWAS_ID_6943,GWAS_ID_6944,GWAS_ID_6945,GWAS_ID_6946,GWAS_ID_6947,GWAS_ID_6948,GWAS_ID_6949 59686 RMVar_ID_59686 Human_SNP_ID_515216959 m1A Human chr12 - 108731470 108731470 108731470 CGGCAGCGGTTGGAGGCTTCGCCCGGCTTTGCAGCGGGGACTTCGGCGGCGGCGCCTCAGGCACC CGGCAGCGGTTGGAGGCTTCGCCCGGCTTTGCCGCGGGGACTTCGGCGGCGGCGCCTCAGGCACC T G CORO1C Ensembl:ENSG00000110880 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:108730424..108731525 26863196 MeRIP-seq:(Medium) rs1328089489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33795,Human_RBP_ID_228614,Human_RBP_ID_811454,Human_RBP_ID_4246288,Human_RBP_ID_8940793,Human_RBP_ID_9322679,Human_RBP_ID_22039535,Human_RBP_ID_22436677,Human_RBP_ID_22910619,Human_RBP_ID_24365943 Human_Splice_Rec_1419845,Human_Splice_Rec_1419913,Human_Splice_Rec_1419939,Human_Splice_Rec_1419993,Human_Splice_Rec_1420043 RMVar_hsa_circ_98336,RMVar_hsa_circ_159621,RMVar_hsa_circ_110657,RMVar_hsa_circ_159622 59687 RMVar_ID_59687 Human_SNP_ID_515229534 m1A Human chr12 - 108785197 108785197 108785197 AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCAATGAGCCGAGATCGCGCCACTGCACTCCAGCC AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCGATGAGCCGAGATCGCGCCACTGCACTCCAGCC T C SSH1 Ensembl:ENSG00000084112 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2003242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_211381,Human_miRNA_ID_220896,Human_miRNA_ID_759432,Human_miRNA_ID_764373 59688 RMVar_ID_59688 Human_SNP_ID_515229535 m1A Human chr12 - 108785197 108785197 108785197 AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCAATGAGCCGAGATCGCGCCACTGCACTCCAGCC AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCCATGAGCCGAGATCGCGCCACTGCACTCCAGCC T G SSH1 Ensembl:ENSG00000084112 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2003242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_211381,Human_miRNA_ID_220896,Human_miRNA_ID_759432,Human_miRNA_ID_764373 59689 RMVar_ID_59689 Human_SNP_ID_515230383 m1A Human chr12 - 108788273 108788273 108788273 CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACACAGGAGATTGAGACCCGGCTCCGGCTGGCGGG CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACTCAGGAGATTGAGACCCGGCTCCGGCTGGCGGG T A SSH1 Ensembl:ENSG00000084112 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3741778 Functional Loss SNV dbSNP153 33..33 33 - - - 59690 RMVar_ID_59690 Human_SNP_ID_515230384 m1A Human chr12 - 108788273 108788273 108788273 CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACACAGGAGATTGAGACCCGGCTCCGGCTGGCGGG CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACGCAGGAGATTGAGACCCGGCTCCGGCTGGCGGG T C SSH1 Ensembl:ENSG00000084112 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3741778 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 59691 RMVar_ID_59691 Human_SNP_ID_515230678 m1A Human chr12 - 108789013 108789013 108789013 CCCGTGTTCCGGAGAAGCCAGCCTCTGGCCCAACCGAACCTCCCCCGTTCCTACCACCAGCAGGC CCCGTGTTCCGGAGAAGCCAGCCTCTGGCCCAGCCGAACCTCCCCCGTTCCTACCACCAGCAGGC T C SSH1 Ensembl:ENSG00000084112 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:108788896..108789100 26863196 MeRIP-seq:(Medium) rs1358512326 Functional Loss SNV dbSNP153 33..33 33 - - - 59692 RMVar_ID_59692 Human_SNP_ID_515306431 m1A Human chr12 - 109092682 109092679 109092683 GAAGAGCCAGCTGTGTTGGGAGGAGACAAAGAAAGCACAAGGAAGAGGCCCAGGAGAGAGGCCCC GAAGAGCCAGCTGTGTTGGGAGGAGACAAAG____CACAAGGAAGAGGCCCAGGAGAGAGGCCCC GCTTT G ALKBH2 Ensembl:ENSG00000189046 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109092493..109092831 26863196 MeRIP-seq:(Medium) rs534683789 Functional Loss DEL dbSNP153,HGVD 32..35 33 - - - Human_RBP_ID_230227,Human_RBP_ID_4249474,Human_RBP_ID_18469238,Human_RBP_ID_18976123,Human_RBP_ID_27805967 59693 RMVar_ID_59693 Human_SNP_ID_515306434 m1A Human chr12 - 109092682 109092682 109092682 GAAGAGCCAGCTGTGTTGGGAGGAGACAAAGAAAGCACAAGGAAGAGGCCCAGGAGAGAGGCCCC GAAGAGCCAGCTGTGTTGGGAGGAGACAAAGATAGCACAAGGAAGAGGCCCAGGAGAGAGGCCCC T A ALKBH2 Ensembl:ENSG00000189046 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109092493..109092831 26863196 MeRIP-seq:(Medium) rs1230878915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230227,Human_RBP_ID_4249474,Human_RBP_ID_18469238,Human_RBP_ID_18976123,Human_RBP_ID_27805967 59694 RMVar_ID_59694 Human_SNP_ID_515306435 m1A Human chr12 - 109092685 109092684 109092686 GGAGAAGAGCCAGCTGTGTTGGGAGGAGACAAAGAAAGCACAAGGAAGAGGCCCAGGAGAGAGGC GGAGAAGAGCCAGCTGTGTTGGGAGGAGACA__GAAAGCACAAGGAAGAGGCCCAGGAGAGAGGC CTT C ALKBH2 Ensembl:ENSG00000189046 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:109092576..109092783;chr12:109092501..109092934;chr12:109092551..109092826 26863196 MeRIP-seq:(Medium) rs746333067 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_230227,Human_RBP_ID_4249474,Human_RBP_ID_5490812,Human_RBP_ID_18469238,Human_RBP_ID_18976123,Human_RBP_ID_27805967 59695 RMVar_ID_59695 Human_SNP_ID_515306436 m1A Human chr12 - 109092685 109092685 109092685 GGAGAAGAGCCAGCTGTGTTGGGAGGAGACAAAGAAAGCACAAGGAAGAGGCCCAGGAGAGAGGC GGAGAAGAGCCAGCTGTGTTGGGAGGAGACAACGAAAGCACAAGGAAGAGGCCCAGGAGAGAGGC T G ALKBH2 Ensembl:ENSG00000189046 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:109092576..109092783;chr12:109092501..109092934;chr12:109092551..109092826 26863196 MeRIP-seq:(Medium) rs771439989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230227,Human_RBP_ID_4249474,Human_RBP_ID_5490812,Human_RBP_ID_18469238,Human_RBP_ID_18976123,Human_RBP_ID_27805967 59696 RMVar_ID_59696 Human_SNP_ID_515306650 m1A Human chr12 - 109093418 109093418 109093418 CAGGGTGACTGCGGGATTCCGATCTGCGCCGGAGCTGCGATGCTAGAGCACTCTTGCCACCCCCA CAGGGTGACTGCGGGATTCCGATCTGCGCCGGGGCTGCGATGCTAGAGCACTCTTGCCACCCCCA T C ALKBH2 Ensembl:ENSG00000189046 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:109093282..109093450 26863196 MeRIP-seq:(Medium) rs1008898916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1463582,Human_RBP_ID_11797911,Human_RBP_ID_22792852 Human_Splice_Rec_1420445,Human_Splice_Rec_1420465 59697 RMVar_ID_59697 Human_SNP_ID_515308087 m1A Human chr12 + 109098384 109098384 109098384 GGGGGTTGGGCCGGAAGCTGCGGACGCCTGGGAAGGGGCCGCTGCAGCTCTTGAGCCGCCTCTGC GGGGGTTGGGCCGGAAGCTGCGGACGCCTGGGGAGGGGCCGCTGCAGCTCTTGAGCCGCCTCTGC A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:109098380..109098603 26863196 MeRIP-seq:(Medium) rs753209535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246290,Human_RBP_ID_19056748 RMVar_hsa_circ_159672,RMVar_hsa_circ_89852 59698 RMVar_ID_59698 Human_SNP_ID_515309682 m1A Human chr12 - 109103560 109103560 109103560 TTCTTCTGAGCATAAGAGCCCCAGAGCAAGAAAACAAGGCCATTCGAGTTCTGATTTAGCCAGGA TTCTTCTGAGCATAAGAGCCCCAGAGCAAGAAGACAAGGCCATTCGAGTTCTGATTTAGCCAGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:109101971..109105096 32194978 MeRIP-seq:(Medium) rs1214243361 Functional Loss SNV dbSNP153 33..33 33 - - - 59699 RMVar_ID_59699 Human_SNP_ID_515333268 m1A Human chr12 - 109199528 109199528 109199528 GCAGTCACCTCCATCTCAGCGTAGCTGCTCCCAGCCTCAACGTGGCCCCCATCCTCCACTGTGTA GCAGTCACCTCCATCTCAGCGTAGCTGCTCCCTGCCTCAACGTGGCCCCCATCCTCCACTGTGTA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:109199430..109199616 26863196 MeRIP-seq:(Medium) rs1236386107 Functional Loss SNV dbSNP153 33..33 33 - - - 59700 RMVar_ID_59700 Human_SNP_ID_515344690 m1A Human chr12 - 109239964 109239964 109239964 AAAGGCGAGACCTTGAAGGGGTCCATGATGACAGTGGGCACGAAGTTGAGGAAGATGTGGTTGCA AAAGGCGAGACCTTGAAGGGGTCCATGATGACGGTGGGCACGAAGTTGAGGAAGATGTGGTTGCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:109239926..109240058 26863196 MeRIP-seq:(Medium) rs778843959 Functional Loss SNV dbSNP153 33..33 33 - - - 59701 RMVar_ID_59701 Human_SNP_ID_515344691 m1A Human chr12 - 109239964 109239964 109239964 AAAGGCGAGACCTTGAAGGGGTCCATGATGACAGTGGGCACGAAGTTGAGGAAGATGTGGTTGCA AAAGGCGAGACCTTGAAGGGGTCCATGATGACCGTGGGCACGAAGTTGAGGAAGATGTGGTTGCA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:109239926..109240058 26863196 MeRIP-seq:(Medium) rs778843959 Functional Loss SNV dbSNP153 33..33 33 - - - 59702 RMVar_ID_59702 Human_SNP_ID_515362330 m1A Human chr12 - 109309988 109309988 109309988 CTGGGCTCGCGGCGCCGTACCCCGAACGCCGCAGCCTCCGCCTCCGCCGCCGCCGCCACCGCCAC CTGGGCTCGCGGCGCCGTACCCCGAACGCCGCCGCCTCCGCCTCCGCCGCCGCCGCCACCGCCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109309802..109310004 26863196 MeRIP-seq:(Medium) rs866320310 Functional Loss SNV dbSNP153 33..33 33 - - - 59703 RMVar_ID_59703 Human_SNP_ID_515398086 m1A Human chr12 + 109450360 109450357 109450360 CTGCGCCCAGCCGGGCTCCAGCAGGGGCCGCCACCTGTGCCCCACAAGCACACGTCCCCACCCAC CTGCGCCCAGCCGGGCTCCAGCAGGGGCCG___CCTGTGCCCCACAAGCACACGTCCCCACCCAC GCCA G MYO1H Ensembl:ENSG00000174527 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:109450311..109450440 26863196 MeRIP-seq:(Medium) rs1449798052 Functional Loss DEL dbSNP153 31..33 33 - - - 59704 RMVar_ID_59704 Human_SNP_ID_515398088 m1A Human chr12 + 109450360 109450360 109450360 CTGCGCCCAGCCGGGCTCCAGCAGGGGCCGCCACCTGTGCCCCACAAGCACACGTCCCCACCCAC CTGCGCCCAGCCGGGCTCCAGCAGGGGCCGCCGCCTGTGCCCCACAAGCACACGTCCCCACCCAC A G MYO1H Ensembl:ENSG00000174527 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:109450311..109450440 26863196 MeRIP-seq:(Medium) rs1479494496 Functional Loss SNV dbSNP153 33..33 33 - - - 59705 RMVar_ID_59705 Human_SNP_ID_515398450 m1A Human chr12 + 109451736 109451736 109451736 GCCCCGCCTGTGGCCTCCAGGAGCGCATTGTCAGGTCCCCGGCCATCCTGGGCCTCATACAGCAA GCCCCGCCTGTGGCCTCCAGGAGCGCATTGTCGGGTCCCCGGCCATCCTGGGCCTCATACAGCAA A G MYO1H Ensembl:ENSG00000174527 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109451685..109451790 26863196 MeRIP-seq:(Medium) rs1474673348 Functional Loss SNV dbSNP153 33..33 33 - - - 59706 RMVar_ID_59706 Human_SNP_ID_515404634 m1A Human chr12 - 109477723 109477723 109477723 CCGGAGGTCCCCGCACTTGGGGTCGGGGCCGCAGCTGCCACTGTCTCAGCCCAAAACACCCGAGT CCGGAGGTCCCCGCACTTGGGGTCGGGGCCGCGGCTGCCACTGTCTCAGCCCAAAACACCCGAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:109477674..109477825;chr12:109477675..109477913 26863196 MeRIP-seq:(Medium) rs1274273859 Functional Loss SNV dbSNP153 33..33 33 - - - 59707 RMVar_ID_59707 Human_SNP_ID_515431864 m1A Human chr12 - 109586102 109586102 109586102 CACACCTACCCCAGGTGCTGACAGCATTGTCCACTCCGGAGGGGTTCCCGTGAATCATTCTCTCC CACACCTACCCCAGGTGCTGACAGCATTGTCCGCTCCGGAGGGGTTCCCGTGAATCATTCTCTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:109586051..109586780 32194978 MeRIP-seq:(Medium) rs104895332 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_199 59708 RMVar_ID_59708 Human_SNP_ID_515434596 m1A Human chr12 + 109596921 109596921 109596921 TGGCCTGTGTTCTTCCTGGCCGCCTGGGTCCAATGCTCAGGTGCTGGGGCCTGGTTCCCGGAGAA TGGCCTGTGTTCTTCCTGGCCGCCTGGGTCCACTGCTCAGGTGCTGGGGCCTGGTTCCCGGAGAA A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs974772518 Functional Loss SNV dbSNP153 33..33 33 - - - 59709 RMVar_ID_59709 Human_SNP_ID_515434597 m1A Human chr12 + 109596921 109596921 109596921 TGGCCTGTGTTCTTCCTGGCCGCCTGGGTCCAATGCTCAGGTGCTGGGGCCTGGTTCCCGGAGAA TGGCCTGTGTTCTTCCTGGCCGCCTGGGTCCAGTGCTCAGGTGCTGGGGCCTGGTTCCCGGAGAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs974772518 Functional Loss SNV dbSNP153 33..33 33 - - - 59710 RMVar_ID_59710 Human_SNP_ID_515500688 m1A Human chr12 - 109857573 109857573 109857573 ATCCTGGAGGTGGAGAAAGAAATGTATGGAGCAGAGTGGCCCAAAGTAGGGGCCACACTGGCGCT ATCCTGGAGGTGGAGAAAGAAATGTATGGAGCCGAGTGGCCCAAAGTAGGGGCCACACTGGCGCT T G GLTP Ensembl:ENSG00000139433 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:109855768..109857870 32194978 MeRIP-seq:(Medium) rs1308696433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23536147 Human_Splice_Rec_1422086,Human_Splice_Rec_1422087,Human_Splice_Rec_1422094,Human_Splice_Rec_1422102,Human_Splice_Rec_1422103,Human_Splice_Rec_1422112,Human_Splice_Rec_1422113,Human_Splice_Rec_1422122,Human_Splice_Rec_1422123,Human_Splice_Rec_1422132,Human_Splice_Rec_1422133 RMVar_hsa_circ_306620,RMVar_hsa_circ_318207 59711 RMVar_ID_59711 Human_SNP_ID_515505931 m1A Human chr12 - 109880355 109880355 109880355 CCTCGACCCCGAAATGGCGCTGCTGGCCGAACACTTGCTGAAGCCGCTGCCCGCGGACAAGCAGA CCTCGACCCCGAAATGGCGCTGCTGGCCGAACCCTTGCTGAAGCCGCTGCCCGCGGACAAGCAGA T G GLTP Ensembl:ENSG00000139433 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109880305..109880456 26863196 MeRIP-seq:(Medium) rs765906968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246963,Human_RBP_ID_8775719 Human_Splice_Rec_1422083,Human_Splice_Rec_1422091,Human_Splice_Rec_1422099,Human_Splice_Rec_1422107,Human_Splice_Rec_1422117,Human_Splice_Rec_1422127 59712 RMVar_ID_59712 Human_SNP_ID_515512856 m1A Human chr12 + 109908635 109908635 109908635 GGAGCAGGAGAATCTGTTGAAGCAGCGGTGGGAGCTAGAGAGGCTGGAGGAAGAGCGAAAGCAGA GGAGCAGGAGAATCTGTTGAAGCAGCGGTGGGGGCTAGAGAGGCTGGAGGAAGAGCGAAAGCAGA A G TCHP Ensembl:ENSG00000139437 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109908545..109908698 26863196 MeRIP-seq:(Medium) rs74774614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3749,Human_RBP_ID_9365535,Human_RBP_ID_26321976,Human_RBP_ID_27805974 Human_Splice_Rec_1422156,Human_Splice_Rec_1422157,Human_Splice_Rec_1422180,Human_Splice_Rec_1422181,Human_Splice_Rec_1422208,Human_Splice_Rec_1422209 RMVar_hsa_circ_5214,RMVar_hsa_circ_39554,RMVar_hsa_circ_39308,RMVar_hsa_circ_347598,RMVar_hsa_circ_365680,RMVar_hsa_circ_71451,RMVar_hsa_circ_359199,RMVar_hsa_circ_17697,RMVar_hsa_circ_350122,RMVar_hsa_circ_159737,RMVar_hsa_circ_330574,RMVar_hsa_circ_159738 59713 RMVar_ID_59713 Human_SNP_ID_515512984 m1A Human chr12 + 109908921 109908921 109908921 GTATAACGCTCAACTCAGCAGACGCACACAGCAGATCCAAGAGGAGCTGGTAAGTCTGAAGAGAC GTATAACGCTCAACTCAGCAGACGCACACAGCGGATCCAAGAGGAGCTGGTAAGTCTGAAGAGAC A G TCHP Ensembl:ENSG00000139437 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109908840..109908971 26863196 MeRIP-seq:(Medium) rs150998390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1422158,Human_Splice_Rec_1422159,Human_Splice_Rec_1422182,Human_Splice_Rec_1422183,Human_Splice_Rec_1422210,Human_Splice_Rec_1422211,Human_Splice_Rec_1422229 RMVar_hsa_circ_5214,RMVar_hsa_circ_39554,RMVar_hsa_circ_39308,RMVar_hsa_circ_347598,RMVar_hsa_circ_365680,RMVar_hsa_circ_71451,RMVar_hsa_circ_359199,RMVar_hsa_circ_17697,RMVar_hsa_circ_350122,RMVar_hsa_circ_159737,RMVar_hsa_circ_330574,RMVar_hsa_circ_159738,RMVar_hsa_circ_51606 59714 RMVar_ID_59714 Human_SNP_ID_515514773 m1A Human chr12 - 109915367 109915367 109915367 AGTGCCAAGAGCAAAGTCACCACCCCAAGACAAGGCCCACAGGGCAGAGCCCTGCCTCTGATGAG AGTGCCAAGAGCAAAGTCACCACCCCAAGACAGGGCCCACAGGGCAGAGCCCTGCCTCTGATGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109915365..109915550 26863196 MeRIP-seq:(Medium) rs3809300 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6950,GWAS_ID_6951 59715 RMVar_ID_59715 Human_SNP_ID_515518718 m1A Human chr12 - 109931239 109931239 109931239 CCTGTTTTTAACCATATGTTCTGTCCCATAGCAGTCATTCACACATGTGAAGAAGACACAAGAAT CCTGTTTTTAACCATATGTTCTGTCCCATAGCGGTCATTCACACATGTGAAGAAGACACAAGAAT T C GIT2 Ensembl:ENSG00000139436 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:109931190..109931291 32194978 MeRIP-seq:(Medium) rs1395188011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17467867 RMVar_hsa_circ_119788,RMVar_hsa_circ_123060,RMVar_hsa_circ_159739,RMVar_hsa_circ_159740 59716 RMVar_ID_59716 Human_SNP_ID_515519156 m1A Human chr12 - 109933148 109933148 109933148 CTGATATGGTGAGGACTTCCCTTCGTTTACTGACGTCCAGTGCCTACCGACTGCAGTCAGAGTGC CTGATATGGTGAGGACTTCCCTTCGTTTACTGGCGTCCAGTGCCTACCGACTGCAGTCAGAGTGC T C GIT2 Ensembl:ENSG00000139436 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:109932989..109933190 32194978 MeRIP-seq:(Medium) rs1363321396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9365538 Human_Splice_Rec_1422280,Human_Splice_Rec_1422314,Human_Splice_Rec_1422348,Human_Splice_Rec_1422384,Human_Splice_Rec_1422416,Human_Splice_Rec_1422450,Human_Splice_Rec_1422454,Human_Splice_Rec_1422486,Human_Splice_Rec_1422492,Human_Splice_Rec_1422500 Human_miRNA_ID_2885261 RMVar_hsa_circ_119788,RMVar_hsa_circ_123060,RMVar_hsa_circ_159739,RMVar_hsa_circ_159740 59717 RMVar_ID_59717 Human_SNP_ID_515520278 m1A Human chr12 - 109938461 109938461 109938461 TGTGGCCCCAAGCCCCACTCTCCCTAGCACCGAAGATGTCATCAGGAAGACTGAACAGATCACCA TGTGGCCCCAAGCCCCACTCTCCCTAGCACCGGAGATGTCATCAGGAAGACTGAACAGATCACCA T C GIT2 Ensembl:ENSG00000139436 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:109938414..109938565 32194978 MeRIP-seq:(Medium) rs1565933454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753794,Human_RBP_ID_9365539,Human_RBP_ID_26321981 Human_Splice_Rec_1422277,Human_Splice_Rec_1422311,Human_Splice_Rec_1422345,Human_Splice_Rec_1422381,Human_Splice_Rec_1422413,Human_Splice_Rec_1422447,Human_Splice_Rec_1422451,Human_Splice_Rec_1422483,Human_Splice_Rec_1422489,Human_Splice_Rec_1422497,Human_Splice_Rec_1422505,Human_Splice_Rec_1422515 Human_miRNA_ID_2722222 RMVar_hsa_circ_65378,RMVar_hsa_circ_119788,RMVar_hsa_circ_123060,RMVar_hsa_circ_7044,RMVar_hsa_circ_159739,RMVar_hsa_circ_159740,RMVar_hsa_circ_22855,RMVar_hsa_circ_290167,RMVar_hsa_circ_298813,RMVar_hsa_circ_366132,RMVar_hsa_circ_159741,RMVar_hsa_circ_359405,RMVar_hsa_circ_271485,RMVar_hsa_circ_159743,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_159744,RMVar_hsa_circ_159742 59718 RMVar_ID_59718 Human_SNP_ID_515520960 m1A Human chr12 - 109941042 109941040 109941042 GGGAGCAGAAGAGTGTATGGGGATAGCAAACAAAGTGTGGTGTGAATAAGGGGGGCTTCTCCACG GGGAGCAGAAGAGTGTATGGGGATAGCAAACA__GTGTGGTGTGAATAAGGGGGGCTTCTCCACG CTT C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109940991..109941138 26863196 MeRIP-seq:(Medium) rs1455160775 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_65378,RMVar_hsa_circ_119788,RMVar_hsa_circ_123060,RMVar_hsa_circ_7044,RMVar_hsa_circ_159739,RMVar_hsa_circ_159740,RMVar_hsa_circ_22855,RMVar_hsa_circ_298813,RMVar_hsa_circ_366132,RMVar_hsa_circ_359405,RMVar_hsa_circ_159743,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_159744 59719 RMVar_ID_59719 Human_SNP_ID_515532609 m1A Human chr12 - 109991747 109991747 109991747 GATTTCACTCTCTTTCCAGATCCTTCCTGGGCATCAGTAAATAGGGGAACGTTTTTATGTGATGA GATTTCACTCTCTTTCCAGATCCTTCCTGGGCGTCAGTAAATAGGGGAACGTTTTTATGTGATGA T C GIT2 Ensembl:ENSG00000139436 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109991697..109991813 26863196 MeRIP-seq:(Medium) rs150511663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246965 Human_Splice_Rec_1422250,Human_Splice_Rec_1422282,Human_Splice_Rec_1422316,Human_Splice_Rec_1422350,Human_Splice_Rec_1422386,Human_Splice_Rec_1422418,Human_Splice_Rec_1422520,Human_Splice_Rec_1422546,Human_Splice_Rec_1422570,Human_Splice_Rec_1422602 RMVar_hsa_circ_6072,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_71444,RMVar_hsa_circ_82793,RMVar_hsa_circ_159750,RMVar_hsa_circ_159753,RMVar_hsa_circ_278122,RMVar_hsa_circ_336994,RMVar_hsa_circ_284875,RMVar_hsa_circ_159756,RMVar_hsa_circ_55687,RMVar_hsa_circ_44807,RMVar_hsa_circ_69661,RMVar_hsa_circ_159759,RMVar_hsa_circ_94871,RMVar_hsa_circ_295931,RMVar_hsa_circ_159758 59720 RMVar_ID_59720 Human_SNP_ID_515533697 m1A Human chr12 + 109996271 109996271 109996271 ACCTGCGGGGAACTAGAGGCCGGGGGACAGCAAAGGCGGCGGTGGCGGCGGCGCTTCCGCTCTAA ACCTGCGGGGAACTAGAGGCCGGGGGACAGCACAGGCGGCGGTGGCGGCGGCGCTTCCGCTCTAA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr12:109996226..109996352;chr12:109996229..109996313 26863196 MeRIP-seq:(Medium) rs563566412 Functional Loss SNV dbSNP153 33..33 33 - - - 59721 RMVar_ID_59721 Human_SNP_ID_515533699 m1A Human chr12 - 109996281 109996275 109996281 CTGGGACCCGTTAGAGCGGAAGCGCCGCCGCCACCGCCGCCTTTGCTGTCCCCCGGCCTCTAGTT CTGGGACCCGTTAGAGCGGAAGCGCCGCCGCC______GCCTTTGCTGTCCCCCGGCCTCTAGTT CGGCGGT C GIT2 Ensembl:ENSG00000139436 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:109996235..109996337 26863196 MeRIP-seq:(Medium) rs937288900 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4246966,Human_RBP_ID_18417507 Human_miRNA_ID_2882666 RMVar_hsa_circ_159759,RMVar_hsa_circ_94871 59722 RMVar_ID_59722 Human_SNP_ID_515534523 m1A Human chr12 + 109999557 109999557 109999557 GACCTCCCGCGCGCCCCGCACCCGACCGGCTCAGCCGGCCGGCAGCGTAACACGCCCTACGCTCG GACCTCCCGCGCGCCCCGCACCCGACCGGCTCCGCCGGCCGGCAGCGTAACACGCCCTACGCTCG A C ANKRD13A Ensembl:ENSG00000076513 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:109999463..109999561 26863410 MeRIP-seq:(Medium) rs551309164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4199861 59723 RMVar_ID_59723 Human_SNP_ID_515534524 m1A Human chr12 + 109999557 109999557 109999557 GACCTCCCGCGCGCCCCGCACCCGACCGGCTCAGCCGGCCGGCAGCGTAACACGCCCTACGCTCG GACCTCCCGCGCGCCCCGCACCCGACCGGCTCGGCCGGCCGGCAGCGTAACACGCCCTACGCTCG A G ANKRD13A Ensembl:ENSG00000076513 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:109999463..109999561 26863410 MeRIP-seq:(Medium) rs551309164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4199861 59724 RMVar_ID_59724 Human_SNP_ID_532673955 m1A Human chr13 - 60029844 60029842 60029844 TTTTCATTCTGTGGAAGTGGAGTCTGTTGAAGAGTTTCAAGCAGGAGATGAGCTATTCTGGCTTA TTTTCATTCTGTGGAAGTGGAGTCTGTTGAAG__TTTCAAGCAGGAGATGAGCTATTCTGGCTTA ACT A DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:60029837..60030004 26863196 MeRIP-seq:(Medium) rs1281969831 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_79097,RMVar_hsa_circ_163587,RMVar_hsa_circ_70153,RMVar_hsa_circ_27294,RMVar_hsa_circ_27879,RMVar_hsa_circ_311181,RMVar_hsa_circ_163602 59725 RMVar_ID_59725 Human_SNP_ID_532673959 m1A Human chr13 + 60029867 60029867 60029867 GCTTGAAACTCTTCAACAGACTCCACTTCCACAGAATGAAAATCCAATAACCCTACCACGAGCTT GCTTGAAACTCTTCAACAGACTCCACTTCCACGGAATGAAAATCCAATAACCCTACCACGAGCTT A G DIAPH3-AS1 Ensembl:ENSG00000227528 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:60029848..60030050 26863196 MeRIP-seq:(Medium) rs924684923 Functional Loss SNV dbSNP153 33..33 33 - - - 59726 RMVar_ID_59726 Human_SNP_ID_532683877 m1A Human chr13 - 60072257 60072257 60072257 AGCATATCTACATCTATAGGTACAGTGGAGAGAGGTAGAGAAGAATTAGATGAGATAGTCTAGGA AGCATATCTACATCTATAGGTACAGTGGAGAGGGGTAGAGAAGAATTAGATGAGATAGTCTAGGA T C DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:60072248..60072342 26863196 MeRIP-seq:(Medium) rs1166071900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6297660,Human_RBP_ID_8394384,Human_RBP_ID_9739470 RMVar_hsa_circ_79097,RMVar_hsa_circ_163587 59727 RMVar_ID_59727 Human_SNP_ID_532690669 m1A Human chr13 - 60101688 60101688 60101688 AGGTCCAGGTGTGGTCATTAGGACTGTAGCTGAGGACAGTGGAAGTGAAGCTTGCATTGGCAAGG AGGTCCAGGTGTGGTCATTAGGACTGTAGCTGGGGACAGTGGAAGTGAAGCTTGCATTGGCAAGG T C DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:60101686..60101833 26863196 MeRIP-seq:(Medium) rs910573990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6297806,Human_RBP_ID_12196243 RMVar_hsa_circ_79097,RMVar_hsa_circ_163587,RMVar_hsa_circ_163603,RMVar_hsa_circ_39265,RMVar_hsa_circ_349274 59728 RMVar_ID_59728 Human_SNP_ID_532764917 m1A Human chr13 + 60405803 60405798 60405804 AATCATGATGTGAGGGTTATGGTGGGAATAACATCATGGTTTTGAAGTATCCTTGGACTGAAGAA AATCATGATGTGAGGGTTATGGTGGGAA______CATGGTTTTGAAGTATCCTTGGACTGAAGAA ATAACAT A TDRD3 Ensembl:ENSG00000083544 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:60405797..60405924 26863196 MeRIP-seq:(Medium) rs980033890 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_2388451 RMVar_hsa_circ_163604,RMVar_hsa_circ_107150 59729 RMVar_ID_59729 Human_SNP_ID_534495609 m1A Human chr13 + 67156293 67156293 67156293 ACTGGACGTGTAGAGGAGCGGATCAGCAGAAGAAGATAGAGGCAGGGGGATGTCAAATGCAGCAT ACTGGACGTGTAGAGGAGCGGATCAGCAGAAGTAGATAGAGGCAGGGGGATGTCAAATGCAGCAT A T AL160254.1 Ensembl:ENSG00000285588 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:67156246..67156416 26863196 MeRIP-seq:(Medium) rs528885413 Functional Loss SNV dbSNP153 33..33 33 - - - 59730 RMVar_ID_59730 Human_SNP_ID_535698142 m1A Human chr13 - 71866436 71866435 71866436 GCAGCAACTGCAACCCCAACCTGGCGGCCGCGAGCAACGGCAGCGGCGGCGGCGGCGGCGGCATC GCAGCAACTGCAACCCCAACCTGGCGGCCGCG_GCAACGGCAGCGGCGGCGGCGGCGGCGGCATC CT C DACH1 Ensembl:ENSG00000276644 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:71866343..71866743 26863410 MeRIP-seq:(Medium) rs772612388 Functional Loss DEL dbSNP153 33..33 33 - - - 59731 RMVar_ID_59731 Human_SNP_ID_535909745 m1A Human chr13 - 72727553 72727553 72727553 TGCTGGGGCGGCGGCGGCGGCCGCGGCGGCGAATCTGAATGCGGTGCGGGAGACCATGGACGGTG TGCTGGGGCGGCGGCGGCGGCCGCGGCGGCGAGTCTGAATGCGGTGCGGGAGACCATGGACGGTG T C MZT1 Ensembl:ENSG00000204899 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:72718960..72727650 26863410 MeRIP-seq:(Medium) rs778115494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230752,Human_RBP_ID_438455,Human_RBP_ID_4276645,Human_RBP_ID_5315488,Human_RBP_ID_5463050,Human_RBP_ID_5492903,Human_RBP_ID_8940976,Human_RBP_ID_9323482,Human_RBP_ID_12202905,Human_RBP_ID_17360699,Human_RBP_ID_17843746,Human_RBP_ID_18417735,Human_RBP_ID_22438329,Human_RBP_ID_23602359 Human_Splice_Rec_1470887 59732 RMVar_ID_59732 Human_SNP_ID_535909776 m1A Human chr13 + 72727585 72727581 72727585 TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGAGGG TTCGCCGCCGCGGCCGCCGCCGCCGCCCC____CCGCTGCTACTCGCCATGGCTAAGGCCGAGGG CAGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:72719026..72727675;chr13:72727452..72727650;chr13:72719001..72727688;chr13:72719026..72727687 26863196 MeRIP-seq:(Medium) rs142438556 Functional Loss DEL dbSNP153 30..33 33 - - - 59733 RMVar_ID_59733 Human_SNP_ID_535909778 m1A Human chr13 + 72727582 72727582 72727582 AGATTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGA AGATTCGCCGCCGCGGCCGCCGCCGCCGCCCCCGCACCGCTGCTACTCGCCATGGCTAAGGCCGA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:72727473..72727687 26863196 MeRIP-seq:(Medium) rs775828017 Functional Loss SNV dbSNP153 33..33 33 - - - 59734 RMVar_ID_59734 Human_SNP_ID_535909779 m1A Human chr13 + 72727582 72727582 72727582 AGATTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGA AGATTCGCCGCCGCGGCCGCCGCCGCCGCCCCGGCACCGCTGCTACTCGCCATGGCTAAGGCCGA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:72727473..72727687 26863196 MeRIP-seq:(Medium) rs775828017 Functional Loss SNV dbSNP153 33..33 33 - - - 59735 RMVar_ID_59735 Human_SNP_ID_535909782 m1A Human chr13 + 72727585 72727584 72727585 TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGAGGG TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGC_CCGCTGCTACTCGCCATGGCTAAGGCCGAGGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:72719026..72727675;chr13:72727452..72727650;chr13:72719001..72727688;chr13:72719026..72727687 26863196 MeRIP-seq:(Medium) rs1212196187 Functional Loss DEL dbSNP153 33..33 33 - - - 59736 RMVar_ID_59736 Human_SNP_ID_535909785 m1A Human chr13 + 72727585 72727585 72727585 TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGAGGG TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCCCCGCTGCTACTCGCCATGGCTAAGGCCGAGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:72719026..72727675;chr13:72727452..72727650;chr13:72719001..72727688;chr13:72719026..72727687 26863196 MeRIP-seq:(Medium) rs749891691 Functional Loss SNV dbSNP153 33..33 33 - - - 59737 RMVar_ID_59737 Human_SNP_ID_535909786 m1A Human chr13 + 72727585 72727585 72727585 TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGAGGG TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCGCCGCTGCTACTCGCCATGGCTAAGGCCGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:72719026..72727675;chr13:72727452..72727650;chr13:72719001..72727688;chr13:72719026..72727687 26863196 MeRIP-seq:(Medium) rs749891691 Functional Loss SNV dbSNP153 33..33 33 - - - 59738 RMVar_ID_59738 Human_SNP_ID_535909787 m1A Human chr13 + 72727585 72727585 72727585 TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCACCGCTGCTACTCGCCATGGCTAAGGCCGAGGG TTCGCCGCCGCGGCCGCCGCCGCCGCCCCAGCTCCGCTGCTACTCGCCATGGCTAAGGCCGAGGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:72719026..72727675;chr13:72727452..72727650;chr13:72719001..72727688;chr13:72719026..72727687 26863196 MeRIP-seq:(Medium) rs749891691 Functional Loss SNV dbSNP153 33..33 33 - - - 59739 RMVar_ID_59739 Human_SNP_ID_535927728 m1A Human chr13 + 72795504 72795504 72795504 TGCGTGACTTTGAGTTGACAGAAGAGCAATATATTAAATTAAAAGCTTTTCCTGAAGATCAGCTT TGCGTGACTTTGAGTTGACAGAAGAGCAATATGTTAAATTAAAAGCTTTTCCTGAAGATCAGCTT A G PIBF1 Ensembl:ENSG00000083535 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1372000 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3944284,Human_RBP_ID_22181605 Human_Splice_Rec_1471203,Human_Splice_Rec_1471235,Human_Splice_Rec_1471261 Human_miRNA_ID_150779,Human_miRNA_ID_1991845 GWAS_ID_6952,GWAS_ID_6953,GWAS_ID_6954,GWAS_ID_6955,GWAS_ID_6956,GWAS_ID_6957,GWAS_ID_6958,GWAS_ID_6959,GWAS_ID_6960 RMVar_hsa_circ_12798,RMVar_hsa_circ_163699,RMVar_hsa_circ_286083,RMVar_hsa_circ_372291,RMVar_hsa_circ_49229,RMVar_hsa_circ_117928,RMVar_hsa_circ_15768,RMVar_hsa_circ_163700,RMVar_hsa_circ_311174,RMVar_hsa_circ_378979,RMVar_hsa_circ_163698,RMVar_hsa_circ_349159,RMVar_hsa_circ_280471,RMVar_hsa_circ_70924,RMVar_hsa_circ_57135,RMVar_hsa_circ_163701,RMVar_hsa_circ_69026,RMVar_hsa_circ_370151,RMVar_hsa_circ_163703 59740 RMVar_ID_59740 Human_SNP_ID_535994627 m1A Human chr13 - 73059055 73059045 73059055 TGCTCTCAGGCTCTCCGGAGCCCGCTCCCGCCACCGCCGACCTCCGCGAGAGAACCGCGAGCGCA TGCTCTCAGGCTCTCCGGAGCCCGCTCCCGCC__________TCCGCGAGAGAACCGCGAGCGCA AGGTCGGCGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr13:73059001..73059557;chr13:73059001..73059375;chr13:73059001..73060597 26863196 MeRIP-seq:(Medium) rs1331946781 Functional Loss DEL dbSNP153 33..42 33 - - - 59741 RMVar_ID_59741 Human_SNP_ID_535994689 m1A Human chr13 - 73059158 73059157 73059159 GGCAGTTTTCGAAGGCGCGCACGAAAAGCAAAACTCTTCCGCTCTTCCACACGTAAACGCCAACG GGCAGTTTTCGAAGGCGCGCACGAAAAGCAA__CTCTTCCGCTCTTCCACACGTAAACGCCAACG GTT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:73059057..73059158 26863410 MeRIP-seq:(Medium) rs1354623346 Functional Loss DEL dbSNP153 32..33 33 - - - 59742 RMVar_ID_59742 Human_SNP_ID_535994715 m1A Human chr13 - 73059226 73059226 73059226 CGGCGAGCTCAGCGCGGGGCTGCCGGCGGAGGAGGGGAGGTTTCGGGTGGACTCCTCAGACAGCG CGGCGAGCTCAGCGCGGGGCTGCCGGCGGAGGGGGGGAGGTTTCGGGTGGACTCCTCAGACAGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:73059001..73060597 26863196 MeRIP-seq:(Medium) rs1182161986 Functional Loss SNV dbSNP153 33..33 33 - - - 59743 RMVar_ID_59743 Human_SNP_ID_535994835 m1A Human chr13 + 73059542 73059530 73059542 GCCCGCGCCCGCGCAGGCCCCGCAGCCGGCCCAGCCGCCCGCCACCGGCCCGCGGCTGCCTCCAG GCCCGCGCCCGCGCAGGCCCC____________GCCGCCCGCCACCGGCCCGCGGCTGCCTCCAG CGCAGCCGGCCCA C KLF5 Ensembl:ENSG00000102554 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:73059501..73059575 26863196 MeRIP-seq:(Medium) rs1006658888 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_230570 Human_Splice_Rec_1471309 59744 RMVar_ID_59744 Human_SNP_ID_535995574 m1A Human chr13 - 73061853 73061853 73061853 GATACTTCTCCATTTCACATCTTGTCTAAAAAAGAAGAGATATAAAATGCATAATCCACCTGATT GATACTTCTCCATTTCACATCTTGTCTAAAAAGGAAGAGATATAAAATGCATAATCCACCTGATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:73061851..73061925 26863196 MeRIP-seq:(Medium) rs529026614 Functional Loss SNV dbSNP153 33..33 33 - - - 59745 RMVar_ID_59745 Human_SNP_ID_729914459 m1A Human chrX - 120250891 120250891 120250891 CCCCCAACAAGAAGAAGCCGCACTCCCCAGCGATTCTGCCCCTTCTTTAAACGTCGCTCCAGTCT CCCCCAACAAGAAGAAGCCGCACTCCCCAGCGCTTCTGCCCCTTCTTTAAACGTCGCTCCAGTCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:120250844..120250954 26863196 MeRIP-seq:(Medium) rs927312675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_726727 59746 RMVar_ID_59746 Human_SNP_ID_729969996 m1A Human chrX - 120560832 120560832 120560832 TCTCCCCCCTCGTTCTGCTCACTCCTGGTGTCAGCCTATCCGCCTTCCCAAACCCTCCCATTCCC TCTCCCCCCTCGTTCTGCTCACTCCTGGTGTCGGCCTATCCGCCTTCCCAAACCCTCCCATTCCC T C CUL4B Ensembl:ENSG00000158290 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:120560618..120560975 26863410 MeRIP-seq:(Medium) rs1197488513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1121309,Human_RBP_ID_5050566,Human_RBP_ID_18964117 59747 RMVar_ID_59747 Human_SNP_ID_729977545 m1A Human chrX + 120604169 120604169 120604169 GCCGGCCTTCCTCGTGTGAGGGGATCTGCCGGACCCCTGCAAATTCAATTTCTTTCCCATTCCGG GCCGGCCTTCCTCGTGTGAGGGGATCTGCCGGTCCCCTGCAAATTCAATTTCTTTCCCATTCCGG A T MCTS1 Ensembl:ENSG00000232119 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:120604118..120604225 26863196 MeRIP-seq:(Medium) rs1013062072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076276,Human_RBP_ID_5432423,Human_RBP_ID_5455133,Human_RBP_ID_5482959,Human_RBP_ID_5517150,Human_RBP_ID_7970582,Human_RBP_ID_8161901,Human_RBP_ID_9250822,Human_RBP_ID_17440037,Human_RBP_ID_18914645,Human_RBP_ID_22468970,Human_RBP_ID_23302354 Human_Splice_Rec_2233003 59748 RMVar_ID_59748 Human_SNP_ID_729981672 m1A Human chrX - 120630001 120630001 120630001 AGAACACCGCCTGCAGCTAGAACAGCCTGGTCAGGAGCGTAACGGAGTGGTGCGCCAACGTGAGA AGAACACCGCCTGCAGCTAGAACAGCCTGGTCTGGAGCGTAACGGAGTGGTGCGCCAACGTGAGA T A C1GALT1C1 Ensembl:ENSG00000171155 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:120629951..120630053 26863196 MeRIP-seq:(Medium) rs1335814275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800209,Human_RBP_ID_5076741,Human_RBP_ID_18454020 Human_Splice_Rec_2233033,Human_Splice_Rec_2233035 59749 RMVar_ID_59749 Human_SNP_ID_730502003 m1A Human chrX - 123614107 123614107 123614107 AATGGACAAGAAAGATTTGGACAAGTCAAGGGAAAGATCCAGAGAAAGAGAGAAAAAAGATGAAA AATGGACAAGAAAGATTTGGACAAGTCAAGGGGAAGATCCAGAGAAAGAGAGAAAAAAGATGAAA T C THOC2 Ensembl:ENSG00000125676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:123614027..123614137 26863196 MeRIP-seq:(Medium) rs1413809073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93738,Human_RBP_ID_968103,Human_RBP_ID_7971673,Human_RBP_ID_16807686,Human_RBP_ID_24549993,Human_RBP_ID_26363309 Human_Splice_Rec_2233253,Human_Splice_Rec_2233254,Human_Splice_Rec_2233268,Human_Splice_Rec_2233269,Human_Splice_Rec_2233338,Human_Splice_Rec_2233339,Human_Splice_Rec_2233347,Human_Splice_Rec_2233352,Human_Splice_Rec_2233353,Human_Splice_Rec_2233369,Human_Splice_Rec_2233370,Human_Splice_Rec_2233381,Human_Splice_Rec_2233382,Human_Splice_Rec_2233397,Human_Splice_Rec_2233398,Human_Splice_Rec_2233468,Human_Splice_Rec_2233469,Human_Splice_Rec_2233531,Human_Splice_Rec_2233532,Human_Splice_Rec_2233541,Human_Splice_Rec_2233542,Human_Splice_Rec_2233549,Human_Splice_Rec_2233550 RMVar_hsa_circ_5358,RMVar_hsa_circ_48249,RMVar_hsa_circ_74592,RMVar_hsa_circ_347580,RMVar_hsa_circ_62422,RMVar_hsa_circ_57296,RMVar_hsa_circ_69162,RMVar_hsa_circ_35666,RMVar_hsa_circ_43514,RMVar_hsa_circ_263705,RMVar_hsa_circ_8038,RMVar_hsa_circ_93198,RMVar_hsa_circ_66083,RMVar_hsa_circ_351081,RMVar_hsa_circ_263707,RMVar_hsa_circ_50180,RMVar_hsa_circ_87585,RMVar_hsa_circ_263708 59750 RMVar_ID_59750 Human_SNP_ID_730513544 m1A Human chrX - 123682495 123682495 123682495 GAGGAAGAGCCTCTAGGCCAAGGGAACAGTCAATGCAATGGCTCTAAGGTGTGAGCATGCCTGAT GAGGAAGAGCCTCTAGGCCAAGGGAACAGTCAGTGCAATGGCTCTAAGGTGTGAGCATGCCTGAT T C THOC2 Ensembl:ENSG00000125676 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:123682444..123682561 26863196 MeRIP-seq:(Medium) rs754407373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24326906 RMVar_hsa_circ_617,RMVar_hsa_circ_5358,RMVar_hsa_circ_53709,RMVar_hsa_circ_57239,RMVar_hsa_circ_54179,RMVar_hsa_circ_21392,RMVar_hsa_circ_14091,RMVar_hsa_circ_54617,RMVar_hsa_circ_43527,RMVar_hsa_circ_32078,RMVar_hsa_circ_281758,RMVar_hsa_circ_42837,RMVar_hsa_circ_297130,RMVar_hsa_circ_351668,RMVar_hsa_circ_344806,RMVar_hsa_circ_351620,RMVar_hsa_circ_336798,RMVar_hsa_circ_18633,RMVar_hsa_circ_50661,RMVar_hsa_circ_32948,RMVar_hsa_circ_36907,RMVar_hsa_circ_311158 59751 RMVar_ID_59751 Human_SNP_ID_730548300 m1A Human chrX - 123859883 123859883 123859883 TTCAACTTACCACTTGGGCCGGGCGTCCCTCGATGAGCGCCACGCCGGCTCCGGGCGCCGCCAAG TTCAACTTACCACTTGGGCCGGGCGTCCCTCGGTGAGCGCCACGCCGGCTCCGGGCGCCGCCAAG T C RF00017-4531,RF00017-4706 RNACentral:URS000098F531,RNACentral:URS000095B12E SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:123859834..123859917 26863196 MeRIP-seq:(Medium) rs1387817585 Functional Loss SNV dbSNP153 33..33 33 - - - 59752 RMVar_ID_59752 Human_SNP_ID_730548376 m1A Human chrX - 123860206 123860206 123860206 AGGGTCCCGGAGGAGGCGCGGCCCGAGCCCCAATCTGGAAATGCCAACTCCGCTCTGCGGCTTGG AGGGTCCCGGAGGAGGCGCGGCCCGAGCCCCAGTCTGGAAATGCCAACTCCGCTCTGCGGCTTGG T C RF00017-4531,RF00017-4706 RNACentral:URS000098F531,RNACentral:URS000095B12E SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:123860173..123860250 26863196 MeRIP-seq:(Medium) rs1169181070 Functional Loss SNV dbSNP153 33..33 33 - - - 59753 RMVar_ID_59753 Human_SNP_ID_730559736 m1A Human chrX + 123912590 123912590 123912590 CTGGGAGGCAGAGGCTGCATTGAGCTATGATCATGGCACTGCATTCCAGCCTGGGTGACAGTGCA CTGGGAGGCAGAGGCTGCATTGAGCTATGATCGTGGCACTGCATTCCAGCCTGGGTGACAGTGCA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs774899728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5078774,Human_RBP_ID_17580508,Human_RBP_ID_26573945 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 59754 RMVar_ID_59754 Human_SNP_ID_731014219 m1A Human chrX + 126473116 126473116 126473116 TACTAACTACCTGACTTCTACCCCTCACAATCATGGCAAGCCAGCGCCACCTATCCAACGAACCA TACTAACTACCTGACTTCTACCCCTCACAATCGTGGCAAGCCAGCGCCACCTATCCAACGAACCA A G MTND4P24 Ensembl:ENSG00000232177 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:126473002..126473205 26863196 MeRIP-seq:(Medium) rs5974657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3272141,Human_RBP_ID_17096348,Human_RBP_ID_17203231,Human_RBP_ID_17443619,Human_RBP_ID_18409825,Human_RBP_ID_18964268,Human_RBP_ID_21959042 59755 RMVar_ID_59755 Human_SNP_ID_731590323 m1A Human chrX - 129523421 129523420 129523421 AGCTCTTTCCAGTGCAGCCACTGCCGCCGCCCAGGAGCCCTCGTCCCCTGCCTTGTCCCCCTACT AGCTCTTTCCAGTGCAGCCACTGCCGCCGCCC_GGAGCCCTCGTCCCCTGCCTTGTCCCCCTACT CT C SMARCA1 Ensembl:ENSG00000102038 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:129523402..129523493 26863410 MeRIP-seq:(Medium) rs770494659 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_800431,Human_RBP_ID_9410142 59756 RMVar_ID_59756 Human_SNP_ID_731593382 m1A Human chrX + 129540346 129540346 129540346 GGCGCCCGGCGCGGAGCTGTTCCTCAAACGACACGCAGCCGAGGTGGGTGGGTGTGGGGACGCGG GGCGCCCGGCGCGGAGCTGTTCCTCAAACGACGCGCAGCCGAGGTGGGTGGGTGTGGGGACGCGG A G OCRL Ensembl:ENSG00000122126 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:129540275..129540566 26863196 MeRIP-seq:(Medium) rs1453006430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5051509 59757 RMVar_ID_59757 Human_SNP_ID_731593396 m1A Human chrX - 129540412 129540412 129540412 TCCATCCAGGCGGCCTCCGGGCTCAGCAGGACAGCGGACTGCGGGCCGATCCGACGACACTGGCT TCCATCCAGGCGGCCTCCGGGCTCAGCAGGACGGCGGACTGCGGGCCGATCCGACGACACTGGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:129540315..129540441 26863196 MeRIP-seq:(Medium) rs1380755597 Functional Loss SNV dbSNP153 33..33 33 - - - 59758 RMVar_ID_59758 Human_SNP_ID_731659024 m1A Human chrX - 129906238 129906238 129906238 ACCCAGAATCCCCCCTCCCCTCGTTGCCCTTCACCTCTCTGCAAGCCGGTTCGCAGTCATTTCAG ACCCAGAATCCCCCCTCCCCTCGTTGCCCTTCCCCTCTCTGCAAGCCGGTTCGCAGTCATTTCAG T G AL034405.1 Ensembl:ENSG00000235189 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chrX:129906198..129906269;chrX:129906198..129906308 26863196 MeRIP-seq:(Medium) rs978548087 Functional Loss SNV dbSNP153 33..33 33 - - - 59759 RMVar_ID_59759 Human_SNP_ID_731660380 m1A Human chrX + 129913371 129913371 129913371 TCAGGTTTAAAGTGTGGCTGCAGGATGAAGGGAGACTTTAGAAAAAAAAAATCAGAGGTAATACA TCAGGTTTAAAGTGTGGCTGCAGGATGAAGGGGGACTTTAGAAAAAAAAAATCAGAGGTAATACA A G UTP14A Ensembl:ENSG00000156697 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:129913364..129919443 32194978 MeRIP-seq:(Medium) rs752829939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7975438,Human_RBP_ID_16816684,Human_RBP_ID_24328425 Human_Splice_Rec_2234974 RMVar_hsa_circ_263852,RMVar_hsa_circ_107002 59760 RMVar_ID_59760 Human_SNP_ID_731661839 m1A Human chrX - 129921349 129921349 129921349 GTGCAGCTCCTGAGCATCCAGGGATTCGGCCCATCTGCATTCATCTGCACTTCATTCACTACATC GTGCAGCTCCTGAGCATCCAGGGATTCGGCCCGTCTGCATTCATCTGCACTTCATTCACTACATC T C AL034405.1 Ensembl:ENSG00000235189 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:129921298..129921396 26863196 MeRIP-seq:(Medium) rs772226470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55805 59761 RMVar_ID_59761 Human_SNP_ID_731661872 m1A Human chrX + 129921503 129921503 129921503 AAAGACCAGTGGCAGAAGAAGAAATTTTGTTGAGAGAATTTGAGGAAAGGCGATCCCTTAGAAAA AAAGACCAGTGGCAGAAGAAGAAATTTTGTTGGGAGAATTTGAGGAAAGGCGATCCCTTAGAAAA A G UTP14A Ensembl:ENSG00000156697 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:129921452..129921614;chrX:129921452..129921617 26863196 MeRIP-seq:(Medium) rs1474925941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3241935,Human_RBP_ID_24328433,Human_RBP_ID_27834807 Human_Splice_Rec_2234938,Human_Splice_Rec_2234966,Human_Splice_Rec_2234984 RMVar_hsa_circ_307698,RMVar_hsa_circ_315574 59762 RMVar_ID_59762 Human_SNP_ID_731662498 m1A Human chrX + 129925062 129925062 129925062 TCCCAGACCTGTGTTAGAAGGGCAGCAGTCAGAGAGGACCCCAAATAATCGCCCTGATGCCCCTA TCCCAGACCTGTGTTAGAAGGGCAGCAGTCAGCGAGGACCCCAAATAATCGCCCTGATGCCCCTA A C UTP14A Ensembl:ENSG00000156697 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:129925012..129925133 26863196 MeRIP-seq:(Medium) rs769273119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24328440,Human_RBP_ID_26363360 59763 RMVar_ID_59763 Human_SNP_ID_731662681 m1A Human chrX - 129926132 129926131 129926133 GGCGAGGGGAGAACCCGGTGCCCTTTTGACAGACTTTCTTCGGCATTCTTACCGGCGTCTTTTCT GGCGAGGGGAGAACCCGGTGCCCTTTTGACA__CTTTCTTCGGCATTCTTACCGGCGTCTTTTCT GTC G AL034405.1 Ensembl:ENSG00000235189 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:129926130..129926218 26863196 MeRIP-seq:(Medium) rs752929332 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_55805 59764 RMVar_ID_59764 Human_SNP_ID_731673484 m1A Human chrX - 129983827 129983827 129983827 TCGCCGACCCCTTGCCTCCAGGCCTGGCGCGAAGCGGGTGGAGGGCTTGCACGCCGGATCTCCCC TCGCCGACCCCTTGCCTCCAGGCCTGGCGCGAGGCGGGTGGAGGGCTTGCACGCCGGATCTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:129983815..129984084 26863196 MeRIP-seq:(Medium) rs1202570106 Functional Loss SNV dbSNP153 33..33 33 - - - 59765 RMVar_ID_59765 Human_SNP_ID_731673577 m1A Human chrX - 129984199 129984199 129984199 GCGGCGGCAACGGCTGCGGCGGCCCCAGCAGGAGCAGCAGCGGCGGCGGCGGCAGCGGCGGCGGC GCGGCGGCAACGGCTGCGGCGGCCCCAGCAGGGGCAGCAGCGGCGGCGGCGGCAGCGGCGGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:129984178..129984258 26863196 MeRIP-seq:(Medium) rs1323369699 Functional Loss SNV dbSNP153 33..33 33 - - - 59766 RMVar_ID_59766 Human_SNP_ID_731673629 m1A Human chrX + 129984374 129984374 129984374 GCGGGGGGGTGGAGCCCCCGACGGGGGGCGGTACGAGCCGGGACGACGACGACGAGGAGCCCCGG GCGGGGGGGTGGAGCCCCCGACGGGGGGCGGTGCGAGCCGGGACGACGACGACGAGGAGCCCCGG A G BCORL1 Ensembl:ENSG00000085185 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:129984364..129984671 26863196 MeRIP-seq:(Medium) rs1392016460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848288,Human_RBP_ID_3930362,Human_RBP_ID_8164633,Human_RBP_ID_8226607,Human_RBP_ID_9340286,Human_RBP_ID_9443332 59767 RMVar_ID_59767 Human_SNP_ID_731676750 m1A Human chrX - 130002325 130002325 130002325 CAGCTCGCCCCTTGATGCACTGATGACTCCCAAATCTGTATCTCTAGCCTTGACCTCTCTCCTTA CAGCTCGCCCCTTGATGCACTGATGACTCCCAGATCTGTATCTCTAGCCTTGACCTCTCTCCTTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:130002315..130002522 26863196 MeRIP-seq:(Medium) rs1354158824 Functional Loss SNV dbSNP153 33..33 33 - - - 59768 RMVar_ID_59768 Human_SNP_ID_731676767 m1A Human chrX + 130002397 130002397 130002397 GGAAGCTCATGAGCTGAGAGAGAAGGTGGGGCAGGGCTGACAACTGGCACAGAGGGAGAGAGATG GGAAGCTCATGAGCTGAGAGAGAAGGTGGGGCGGGGCTGACAACTGGCACAGAGGGAGAGAGATG A G BCORL1 Ensembl:ENSG00000085185 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:130002390..130002478 26863196 MeRIP-seq:(Medium) rs1569360781 Functional Loss SNV dbSNP153 33..33 33 - - - 59769 RMVar_ID_59769 Human_SNP_ID_731676823 m1A Human chrX - 130002705 130002705 130002705 GCTGTTCACCTCTTGCCTTTCTCCTCTCTCTCACACACACACACAATCCCCTCTCCTCCAACTTT GCTGTTCACCTCTTGCCTTTCTCCTCTCTCTCTCACACACACACAATCCCCTCTCCTCCAACTTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130002686..130002951 26863196 MeRIP-seq:(Medium) rs1265811220 Functional Loss SNV dbSNP153 33..33 33 - - - 59770 RMVar_ID_59770 Human_SNP_ID_731681088 m1A Human chrX + 130025263 130025252 130025264 AATGTGGGACACCAATGAGGAGGAGGAGGAAGAAGAGGAGGAGGGCCTGCTGAAGAGGAAGAAAC AATGTGGGACACCAATGAGGAG____________GAGGAGGAGGGCCTGCTGAAGAGGAAGAAAC GGAGGAGGAAGAA G BCORL1 Ensembl:ENSG00000085185 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:130025212..130025317 26863196 MeRIP-seq:(Medium) rs1221525286 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_59862,RMVar_hsa_circ_50941,RMVar_hsa_circ_345740,RMVar_hsa_circ_46663,RMVar_hsa_circ_22078,RMVar_hsa_circ_46503,RMVar_hsa_circ_61992,RMVar_hsa_circ_340451,RMVar_hsa_circ_263855 59771 RMVar_ID_59771 Human_SNP_ID_731696768 m1A Human chrX + 130110702 130110702 130110702 ACACTTCGCGCCGCCAATGGCAAGTTGGAGGGAGAGATGCAAATACCAGGTGAGACGGCGGCGCC ACACTTCGCGCCGCCAATGGCAAGTTGGAGGGGGAGATGCAAATACCAGGTGAGACGGCGGCGCC A G RF00017-8703 RNACentral:URS00009560DA SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:130110554..130110825 26863196 MeRIP-seq:(Medium) rs1220970806 Functional Loss SNV dbSNP153 33..33 33 - - - 59772 RMVar_ID_59772 Human_SNP_ID_731702456 m1A Human chrX - 130142470 130142470 130142470 AATAGGCTGGACGGGGGTGGTGGGGAGCCCTCATGCCTCATGGGAAGCTATGGAAGATCACATCT AATAGGCTGGACGGGGGTGGTGGGGAGCCCTCTTGCCTCATGGGAAGCTATGGAAGATCACATCT T A AIFM1 Ensembl:ENSG00000156709 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130142452..130142577 26863196 MeRIP-seq:(Medium) rs752501973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22632323 RMVar_hsa_circ_38968,RMVar_hsa_circ_35161,RMVar_hsa_circ_367240 59773 RMVar_ID_59773 Human_SNP_ID_731702457 m1A Human chrX - 130142470 130142470 130142470 AATAGGCTGGACGGGGGTGGTGGGGAGCCCTCATGCCTCATGGGAAGCTATGGAAGATCACATCT AATAGGCTGGACGGGGGTGGTGGGGAGCCCTCGTGCCTCATGGGAAGCTATGGAAGATCACATCT T C AIFM1 Ensembl:ENSG00000156709 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130142452..130142577 26863196 MeRIP-seq:(Medium) rs752501973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22632323 RMVar_hsa_circ_38968,RMVar_hsa_circ_35161,RMVar_hsa_circ_367240 59774 RMVar_ID_59774 Human_SNP_ID_731702742 m1A Human chrX - 130144436 130144436 130144436 CTCGATACTGATAGAGCAGTTAGGTACAAGTTAGGAAGTGGCAAGAGATGAACCTGAGAAGTTAT CTCGATACTGATAGAGCAGTTAGGTACAAGTTGGGAAGTGGCAAGAGATGAACCTGAGAAGTTAT T C AIFM1 Ensembl:ENSG00000156709 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130144426..130144550 26863196 MeRIP-seq:(Medium) rs1024134179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16817344 RMVar_hsa_circ_38968,RMVar_hsa_circ_35161,RMVar_hsa_circ_367240 59775 RMVar_ID_59775 Human_SNP_ID_731706615 m1A Human chrX + 130165652 130165652 130165652 TCAAAGCACCCGCCGCCAGGCCTCCACACCGGAACATTTCGGCGACCGCTATTCGGGACCTCCTC TCAAAGCACCCGCCGCCAGGCCTCCACACCGGGACATTTCGGCGACCGCTATTCGGGACCTCCTC A G RF00017-8703 RNACentral:URS00009560DA SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:130165607..130165760 26863196 MeRIP-seq:(Medium) rs1326038976 Functional Loss SNV dbSNP153 33..33 33 - - - 59776 RMVar_ID_59776 Human_SNP_ID_731749065 m1A Human chrX + 130412669 130412669 130412669 CCTCAAGCAGGAGGGAGGCAAGAGAAGAAAAGACCAGGATTAGGGACAGAGGGCGGAGCTCAGAT CCTCAAGCAGGAGGGAGGCAAGAGAAGAAAAGCCCAGGATTAGGGACAGAGGGCGGAGCTCAGAT A C RBMX2 Ensembl:ENSG00000134597 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:130412552..130412682 26863196 MeRIP-seq:(Medium) rs933413450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_728017,Human_RBP_ID_7976024,Human_RBP_ID_16818667 RMVar_hsa_circ_107020,RMVar_hsa_circ_124562,RMVar_hsa_circ_263877,RMVar_hsa_circ_263878 59777 RMVar_ID_59777 Human_SNP_ID_731749066 m1A Human chrX + 130412669 130412669 130412669 CCTCAAGCAGGAGGGAGGCAAGAGAAGAAAAGACCAGGATTAGGGACAGAGGGCGGAGCTCAGAT CCTCAAGCAGGAGGGAGGCAAGAGAAGAAAAGTCCAGGATTAGGGACAGAGGGCGGAGCTCAGAT A T RBMX2 Ensembl:ENSG00000134597 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:130412552..130412682 26863196 MeRIP-seq:(Medium) rs933413450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_728017,Human_RBP_ID_7976024,Human_RBP_ID_16818667 RMVar_hsa_circ_107020,RMVar_hsa_circ_124562,RMVar_hsa_circ_263877,RMVar_hsa_circ_263878 59778 RMVar_ID_59778 Human_SNP_ID_731806724 m1A Human chrX - 130749871 130749871 130749871 AGGCAGAGAGGAATTGATGGATGGACTGAGAGACGGACAGAGAAACAGAAAGAAAAATAGACAGA AGGCAGAGAGGAATTGATGGATGGACTGAGAGGCGGACAGAGAAACAGAAAGAAAAATAGACAGA T C ENOX2 Ensembl:ENSG00000165675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130749867..130749988 26863196 MeRIP-seq:(Medium) rs919650260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364459,RMVar_hsa_circ_354727,RMVar_hsa_circ_263884,RMVar_hsa_circ_375123 59779 RMVar_ID_59779 Human_SNP_ID_731829542 m1A Human chrX - 130900550 130900550 130900550 CAATGTGGAAGAATTCAGCATGGTTGGAGTGCAGATAGTTGAGTAAAAGGAAACTGTAATGGGTA CAATGTGGAAGAATTCAGCATGGTTGGAGTGCCGATAGTTGAGTAAAAGGAAACTGTAATGGGTA T G ENOX2 Ensembl:ENSG00000165675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:130900547..130900703 26863196 MeRIP-seq:(Medium) rs1248684942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7976304,Human_RBP_ID_16818836 59780 RMVar_ID_59780 Human_SNP_ID_731829570 m1A Human chrX - 130900745 130900745 130900745 TGGAGGGATAAAGGAAGGTGTGACTCACTGTAAGGGAGACTCGGGGAGAAGGCTTCCATGAGGAG TGGAGGGATAAAGGAAGGTGTGACTCACTGTACGGGAGACTCGGGGAGAAGGCTTCCATGAGGAG T G ENOX2 Ensembl:ENSG00000165675 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:130900559..130900744 26863196 MeRIP-seq:(Medium) rs899997220 Functional Loss SNV dbSNP153 33..33 33 - - - 59781 RMVar_ID_59781 Human_SNP_ID_731829983 m1A Human chrX + 130903158 130903158 130903158 CGTAGTGCCCTCGCGGCGCCCCACGCCGCGCCACTCTCTTCCGAAATGCCCGCCTCGCGCTTCCA CGTAGTGCCCTCGCGGCGCCCCACGCCGCGCCCCTCTCTTCCGAAATGCCCGCCTCGCGCTTCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:130903107..130903182 26863196 MeRIP-seq:(Medium) rs901953314 Functional Loss SNV dbSNP153 33..33 33 - - - 59782 RMVar_ID_59782 Human_SNP_ID_731975914 m1A Human chrX - 131713755 131713755 131713755 GTAGAAGGATTATAGGGTGGAAGAGCGGAGGCAGAGGAAGAATTGGGACCTAGCTCGGCCTGGCG GTAGAAGGATTATAGGGTGGAAGAGCGGAGGCTGAGGAAGAATTGGGACCTAGCTCGGCCTGGCG T A FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:131713579..131713883 26863196 MeRIP-seq:(Medium) rs142231419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263889,RMVar_hsa_circ_92929,RMVar_hsa_circ_311647,RMVar_hsa_circ_263890,RMVar_hsa_circ_263891,RMVar_hsa_circ_314230,RMVar_hsa_circ_362082,RMVar_hsa_circ_268761 59783 RMVar_ID_59783 Human_SNP_ID_731976255 m1A Human chrX - 131715352 131715352 131715352 AGTCTAAGTGAAGGCAAAGAGAGGCTGGGACGAGGGGTGCAGGGGAACAGTAAAGAAAGCATGTT AGTCTAAGTGAAGGCAAAGAGAGGCTGGGACGGGGGGTGCAGGGGAACAGTAAAGAAAGCATGTT T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:131715240..131715378 26863196 MeRIP-seq:(Medium) rs185201832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263889,RMVar_hsa_circ_92929,RMVar_hsa_circ_311647,RMVar_hsa_circ_263890,RMVar_hsa_circ_263891,RMVar_hsa_circ_314230,RMVar_hsa_circ_362082,RMVar_hsa_circ_268761 59784 RMVar_ID_59784 Human_SNP_ID_732032542 m1A Human chrX + 132023326 132023326 132023326 GGAGCGGCATCACTCGAGCCCAGGTCCCAGCCACCACCACTCACAGCGCTCGGCGTTCAGGAAGA GGAGCGGCATCACTCGAGCCCAGGTCCCAGCCGCCACCACTCACAGCGCTCGGCGTTCAGGAAGA A G STK26 Ensembl:ENSG00000134602 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:132023276..132023375 26863196 MeRIP-seq:(Medium) rs762145557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076300,Human_RBP_ID_5483007 Human_Splice_Rec_2236437,Human_Splice_Rec_2236459,Human_Splice_Rec_2236480,Human_Splice_Rec_2236500 59785 RMVar_ID_59785 Human_SNP_ID_732032567 m1A Human chrX - 132023409 132023409 132023409 TGTTAGCGGCGCAGCTCCCTGGGACTCAGTCTACCTTTCTGGCGCCCGCCCGCCGCTGAAGCAGC TGTTAGCGGCGCAGCTCCCTGGGACTCAGTCTCCCTTTCTGGCGCCCGCCCGCCGCTGAAGCAGC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:132023319..132023505 26863196 MeRIP-seq:(Medium) rs1391486741 Functional Loss SNV dbSNP153 33..33 33 - - - 59786 RMVar_ID_59786 Human_SNP_ID_732109297 m1A Human chrX - 132489908 132489908 132489908 GCGACTTTTTGGCGCTCTTTGGGAGCAGTGAGAGAGAGGCGGAGGCCAGAGAGTCCGGGGTGGGC GCGACTTTTTGGCGCTCTTTGGGAGCAGTGAGGGAGAGGCGGAGGCCAGAGAGTCCGGGGTGGGC T C MBNL3 Ensembl:ENSG00000076770 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:132489858..132489991 26863196 MeRIP-seq:(Medium) rs1383462387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5075893,Human_RBP_ID_5483677,Human_RBP_ID_8226616,Human_RBP_ID_23107668 Human_Splice_Rec_2236722,Human_Splice_Rec_2236752 59787 RMVar_ID_59787 Human_SNP_ID_732109314 m1A Human chrX - 132489988 132489988 132489988 AACCACACAAAGAATATATTTCGCGACGAAACAGCGCCCTACAGGAAGAAAGTGCCCGCACTCCG AACCACACAAAGAATATATTTCGCGACGAAACGGCGCCCTACAGGAAGAAAGTGCCCGCACTCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:132489821..132489994 26863196 MeRIP-seq:(Medium) rs906439926 Functional Loss SNV dbSNP153 33..33 33 - - - 59788 RMVar_ID_59788 Human_SNP_ID_732165171 m1A Human chrX + 132823843 132823843 132823843 CACCACTGTACTCCAGCCTGGGCAAGAGTGAGACTTCATAAAAAATAATAATAATAATAATAATA CACCACTGTACTCCAGCCTGGGCAAGAGTGAGGCTTCATAAAAAATAATAATAATAATAATAATA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:132823717..132823844 26863196 MeRIP-seq:(Medium) rs1203874622 Functional Loss SNV dbSNP153 33..33 33 - - - 59789 RMVar_ID_59789 Human_SNP_ID_732183187 m1A Human chrX + 132927205 132927204 132927205 TTACTCGCAGCATTCTTTCTGTTCTTCCTCCTAAACCTCCTGAATCCATTCACCTCTCTGCATCC TTACTCGCAGCATTCTTTCTGTTCTTCCTCCT_AACCTCCTGAATCCATTCACCTCTCTGCATCC TA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:132927195..132927279 26863196 MeRIP-seq:(Medium) rs1401581226 Functional Loss DEL dbSNP153 33..33 33 - - - 59790 RMVar_ID_59790 Human_SNP_ID_732188719 m1A Human chrX - 132958493 132958493 132958493 CTGTCCCCGCCGGCATTCCAGAGTAGAGGCCGAATTGGCAGCGAGCCGGCCCGGGTCGGTCGCCG CTGTCCCCGCCGGCATTCCAGAGTAGAGGCCGGATTGGCAGCGAGCCGGCCCGGGTCGGTCGCCG T C HS6ST2 Ensembl:ENSG00000171004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:132958443..132958560 26863196 MeRIP-seq:(Medium) rs1219155715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_728410 59791 RMVar_ID_59791 Human_SNP_ID_732266798 m1A Human chrX + 133415080 133415080 133415080 GTCGGGGACTAGCGAGTGGAGCTGGAGGGAGAAGGAGTTGGAGTTGGTGGAAGAGGCGAGCAGGC GTCGGGGACTAGCGAGTGGAGCTGGAGGGAGACGGAGTTGGAGTTGGTGGAAGAGGCGAGCAGGC A C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:133414993..133415093 26863196 MeRIP-seq:(Medium) rs1442299630 Functional Loss SNV dbSNP153 33..33 33 - - - 59792 RMVar_ID_59792 Human_SNP_ID_732356656 m1A Human chrX - 133985743 133985743 133985743 GGCCCCCGCCGCGCTCCACGCCGCGCCCCCGCACCCCGCCGGCTACCGGCCGCACAACCGCCACC GGCCCCCGCCGCGCTCCACGCCGCGCCCCCGCCCCCCGCCGGCTACCGGCCGCACAACCGCCACC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chrX:133985549..133985895;chrX:133985541..133985895;chrX:133985648..133985796 26863410 MeRIP-seq:(Medium) rs1002910014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5075903 59793 RMVar_ID_59793 Human_SNP_ID_732356670 m1A Human chrX + 133985784 133985784 133985784 GCGGCGTGGAGCGCGGCGGGGGCCACTGGGGCACCGCGGCGCGGGGACCGGGCGAAGGCAGTGCG GCGGCGTGGAGCGCGGCGGGGGCCACTGGGGCGCCGCGGCGCGGGGACCGGGCGAAGGCAGTGCG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrX:133985697..133985796 26863410 MeRIP-seq:(Medium) rs1478725814 Functional Loss SNV dbSNP153 33..33 33 - - - 59794 RMVar_ID_59794 Human_SNP_ID_732431491 m1A Human chrX + 134427272 134427272 134427272 GCCATTGGGTTTTTGTGTGTATGTGATTTTCAAAATTCATGACTTGAAGTGCAAGGACAGATCTA GCCATTGGGTTTTTGTGTGTATGTGATTTTCAGAATTCATGACTTGAAGTGCAAGGACAGATCTA A G PHF6 Ensembl:ENSG00000156531 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:134427197..134427397 32194978 MeRIP-seq:(Medium) rs1361466966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_728657,Human_RBP_ID_1061176,Human_RBP_ID_1341172,Human_RBP_ID_2070694,Human_RBP_ID_3916712,Human_RBP_ID_7978465,Human_RBP_ID_8226842,Human_RBP_ID_8933070,Human_RBP_ID_9243612,Human_RBP_ID_16824827,Human_RBP_ID_17552903,Human_RBP_ID_18402867,Human_RBP_ID_18915723,Human_RBP_ID_23217004,Human_RBP_ID_24330000,Human_RBP_ID_24444285,Human_RBP_ID_24525849,Human_RBP_ID_27790673 RMVar_hsa_circ_122191,RMVar_hsa_circ_263941,RMVar_hsa_circ_109681,RMVar_hsa_circ_263943 59795 RMVar_ID_59795 Human_SNP_ID_732437175 m1A Human chrX - 134460251 134460251 134460251 TGCTCAGGAGGAGGAAGCCGGTGGCGGAGCAGAGGAGGAGGCGGAGGCGCAGCAAGAGGCGGCGC TGCTCAGGAGGAGGAAGCCGGTGGCGGAGCAGCGGAGGAGGCGGAGGCGCAGCAAGAGGCGGCGC T G RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:134460152..134460350 26863196 MeRIP-seq:(Medium) rs1401506683 Functional Loss SNV dbSNP153 33..33 33 - - - 59796 RMVar_ID_59796 Human_SNP_ID_732442893 m1A Human chrX + 134493526 134493526 134493526 TTCTTTTTTGAAAGGATATAATTGACACTGGCAAAACAATGCAGACTTTGCTTTCCTTGGTCAGG TTCTTTTTTGAAAGGATATAATTGACACTGGCGAAACAATGCAGACTTTGCTTTCCTTGGTCAGG A G HPRT1 Ensembl:ENSG00000165704 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1240182715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2070761,Human_RBP_ID_16826152,Human_RBP_ID_18155989,Human_RBP_ID_18915756,Human_RBP_ID_22777777,Human_RBP_ID_24330139,Human_RBP_ID_27790718 Human_Splice_Rec_2237047,Human_Splice_Rec_2237048,Human_Splice_Rec_2237063,Human_Splice_Rec_2237064,Human_Splice_Rec_2237075,Human_Splice_Rec_2237076 Human_miRNA_ID_982546,Human_miRNA_ID_987266,Human_miRNA_ID_2446113,Human_miRNA_ID_2447502 RMVar_hsa_circ_11361,RMVar_hsa_circ_263949,RMVar_hsa_circ_272390,RMVar_hsa_circ_288322,RMVar_hsa_circ_291941,RMVar_hsa_circ_109760,RMVar_hsa_circ_263947,RMVar_hsa_circ_263948,RMVar_hsa_circ_344577,RMVar_hsa_circ_263946,RMVar_hsa_circ_355916,RMVar_hsa_circ_327265 59797 RMVar_ID_59797 Human_SNP_ID_732446013 m1A Human chrX + 134512187 134512187 134512187 GACATGCAGGAGATGAGGGGACAGTGAAGAGGATTTCTAAGAACACTCCAGGCAGACAGAACAGC GACATGCAGGAGATGAGGGGACAGTGAAGAGGGTTTCTAAGAACACTCCAGGCAGACAGAACAGC A G HPRT1 Ensembl:ENSG00000165704 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:134512138..134512306 26863196 MeRIP-seq:(Medium) rs1274508887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16826790 59798 RMVar_ID_59798 Human_SNP_ID_732492462 m1A Human chrX + 134796263 134796263 134796263 GGCAGTGCTCAGCTCCTGGTGCTTAGCTATGGACTCCCAAGACTCTCACTGCAGGACTGAGCTGC GGCAGTGCTCAGCTCCTGGTGCTTAGCTATGGGCTCCCAAGACTCTCACTGCAGGACTGAGCTGC A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:134796213..134796299 26863196 MeRIP-seq:(Medium) rs879119890 Functional Loss SNV dbSNP153 33..33 33 - - - 59799 RMVar_ID_59799 Human_SNP_ID_732492504 m1A Human chrX + 134796437 134796437 134796437 AGGAAGGGAGGATGATGGTGAGGCAGGAGAGGAGGACGAAGAGGTAGTGGTGGAAGGTGACAGAA AGGAAGGGAGGATGATGGTGAGGCAGGAGAGGGGGACGAAGAGGTAGTGGTGGAAGGTGACAGAA A G FAM122C Ensembl:ENSG00000156500 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:134796390..134796820 26863196 MeRIP-seq:(Medium) rs1457995791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2237290,Human_Splice_Rec_2237296 59800 RMVar_ID_59800 Human_SNP_ID_732492515 m1A Human chrX + 134796468 134796465 134796469 GAGGACGAAGAGGTAGTGGTGGAAGGTGACAGAATGAAGGAAAAGGATGAAGGAAAGAAGGATGG GAGGACGAAGAGGTAGTGGTGGAAGGTGAC____TGAAGGAAAAGGATGAAGGAAAGAAGGATGG CAGAA C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:134796420..134796571 26863196 MeRIP-seq:(Medium) rs1184472173 Functional Loss DEL dbSNP153 31..34 33 - - - 59801 RMVar_ID_59801 Human_SNP_ID_732492554 m1A Human chrX - 134796667 134796667 134796667 CTTCTTTCCCGCCCCTGCGCTTCTTTTCCCTTACCCTCTGTCCTCCTCCCTCCCCTCTGCCCTCT CTTCTTTCCCGCCCCTGCGCTTCTTTTCCCTTCCCCTCTGTCCTCCTCCCTCCCCTCTGCCCTCT T G FAM122B Ensembl:ENSG00000156504 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:134796637..134796886 32194978 MeRIP-seq:(Medium) rs1290837400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_728911,Human_RBP_ID_3930729,Human_RBP_ID_17580379,Human_RBP_ID_18963682,Human_RBP_ID_21872592,Human_RBP_ID_23098931,Human_RBP_ID_26260174 Human_miRNA_ID_828412,Human_miRNA_ID_848417,Human_miRNA_ID_1368068,Human_miRNA_ID_1387132 59802 RMVar_ID_59802 Human_SNP_ID_732492630 m1A Human chrX + 134797010 134797007 134797011 GCTTCTCCCCTCCCTGCCCCCCTCCCGCCTCGAGGACAGGTTGGGGGTTCGGCCTCTCAGCCGCC GCTTCTCCCCTCCCTGCCCCCCTCCCGCCT____GACAGGTTGGGGGTTCGGCCTCTCAGCCGCC TCGAG T FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:134796959..134797189;chrX:134796959..134797200 26863196 MeRIP-seq:(Medium) rs1353900416 Functional Loss DEL dbSNP153 31..34 33 - - - 59803 RMVar_ID_59803 Human_SNP_ID_732526434 m1A Human chrX - 134991048 134991048 134991048 CACCGACCGTGGGACAGAGGGATGGACGCGGGAAAGTACGGGCGGGAGGCCTCCTGGGCTGCTGC CACCGACCGTGGGACAGAGGGATGGACGCGGGGAAGTACGGGCGGGAGGCCTCCTGGGCTGCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:134991001..134991263 26863196 MeRIP-seq:(Medium) rs1452387996 Functional Loss SNV dbSNP153 33..33 33 - - - 59804 RMVar_ID_59804 Human_SNP_ID_732526661 m1A Human chrX - 134992182 134992182 134992182 CCCCTCAGCTCTCCTTCCCCCTGAATATAGTCATATCACTAATTTTTAACTCTTCTGTTGGCTAC CCCCTCAGCTCTCCTTCCCCCTGAATATAGTCGTATCACTAATTTTTAACTCTTCTGTTGGCTAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:134992131..134992275 26863196 MeRIP-seq:(Medium) rs1462994374 Functional Loss SNV dbSNP153 33..33 33 - - - 59805 RMVar_ID_59805 Human_SNP_ID_732526663 m1A Human chrX + 134992189 134992188 134992189 ACAGAAGAGTTAAAAATTAGTGATATGACTATATTCAGGGGGAAGGAGAGCTGAGGGGGGCGGCA ACAGAAGAGTTAAAAATTAGTGATATGACTAT_TTCAGGGGGAAGGAGAGCTGAGGGGGGCGGCA TA T SMIM10 Ensembl:ENSG00000184785 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:134992140..134992328 26863196 MeRIP-seq:(Medium) rs1273361493 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17667167,Human_RBP_ID_26569518 59806 RMVar_ID_59806 Human_SNP_ID_464050846 m1A Human chr11 - 43312061 43312061 43312061 CCTTGTCCTGACCGGCGCCACCGCCGCCTCGGAACTTCTCCAAACCCACTACCCGCACTATTACA CCTTGTCCTGACCGGCGCCACCGCCGCCTCGGTACTTCTCCAAACCCACTACCCGCACTATTACA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:43311976..43312200 26863196 MeRIP-seq:(Medium) rs1298795241 Functional Loss SNV dbSNP153 33..33 33 - - - 59807 RMVar_ID_59807 Human_SNP_ID_464058360 m1A Human chr11 + 43342521 43342521 43342521 TAGTCGGGGAAGACTCTACTGAATAAGACATCAGCATTCTTCAGCATTGTCATGAGCTTAATATA TAGTCGGGGAAGACTCTACTGAATAAGACATCGGCATTCTTCAGCATTGTCATGAGCTTAATATA A G API5 Ensembl:ENSG00000166181 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:43342451..43342575 32194978 MeRIP-seq:(Medium) rs766596374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1456917,Human_RBP_ID_1779233,Human_RBP_ID_26890507,Human_RBP_ID_27201391 Human_Splice_Rec_1229890,Human_Splice_Rec_1229918,Human_Splice_Rec_1229946,Human_Splice_Rec_1229970,Human_Splice_Rec_1229996 RMVar_hsa_circ_92063,RMVar_hsa_circ_78803,RMVar_hsa_circ_149211,RMVar_hsa_circ_149212,RMVar_hsa_circ_109079,RMVar_hsa_circ_149214 59808 RMVar_ID_59808 Human_SNP_ID_464084115 m1A Human chr11 - 43443446 43443446 43443446 AGACGCCGCCCTTTCATCTCTAGTGCACCCCCAAAGCCTTCCAAAGGCCATGCCTGTTGAAATTC AGACGCCGCCCTTTCATCTCTAGTGCACCCCCGAAGCCTTCCAAAGGCCATGCCTGTTGAAATTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:43443400..43443518 26863196 MeRIP-seq:(Medium) rs765811505 Functional Loss SNV dbSNP153 33..33 33 - - - 59809 RMVar_ID_59809 Human_SNP_ID_464140712 m1A Human chr11 + 43680824 43680824 43680824 TTCATTCACGAAGGTAGTGAGGCCTAGTGGAAAGCCATGGAGAGCGCTCTCCCCGCCGCCGGCTT TTCATTCACGAAGGTAGTGAGGCCTAGTGGAAGGCCATGGAGAGCGCTCTCCCCGCCGCCGGCTT A G AC068205.2,HSD17B12 Ensembl:ENSG00000283341,Ensembl:ENSG00000149084 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:43680775..43680892 26863196 MeRIP-seq:(Medium) rs368642264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227413,Human_RBP_ID_868865,Human_RBP_ID_4160103,Human_RBP_ID_11619679,Human_RBP_ID_17796017,Human_RBP_ID_18416544,Human_RBP_ID_18468911,Human_RBP_ID_22433466,Human_RBP_ID_23505178 Human_miRNA_ID_256838,Human_miRNA_ID_260630 RMVar_hsa_circ_991 59810 RMVar_ID_59810 Human_SNP_ID_464140713 m1A Human chr11 + 43680824 43680824 43680824 TTCATTCACGAAGGTAGTGAGGCCTAGTGGAAAGCCATGGAGAGCGCTCTCCCCGCCGCCGGCTT TTCATTCACGAAGGTAGTGAGGCCTAGTGGAATGCCATGGAGAGCGCTCTCCCCGCCGCCGGCTT A T AC068205.2,HSD17B12 Ensembl:ENSG00000283341,Ensembl:ENSG00000149084 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:43680775..43680892 26863196 MeRIP-seq:(Medium) rs368642264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227413,Human_RBP_ID_868865,Human_RBP_ID_4160103,Human_RBP_ID_11619679,Human_RBP_ID_17796017,Human_RBP_ID_18416544,Human_RBP_ID_18468911,Human_RBP_ID_22433466,Human_RBP_ID_23505178 Human_miRNA_ID_256838,Human_miRNA_ID_260630 RMVar_hsa_circ_991 59811 RMVar_ID_59811 Human_SNP_ID_464199969 m1A Human chr11 - 43942715 43942715 43942715 GGCGCTCCTCGGGAGGGCGGGCGGGCGGGCGGACCCGTCGGGGGGCACGGGGCTCGGGGGGCGCT GGCGCTCCTCGGGAGGGCGGGCGGGCGGGCGGGCCCGTCGGGGGGCACGGGGCTCGGGGGGCGCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:43942614..43942839 26863410 MeRIP-seq:(Medium) rs1403410563 Functional Loss SNV dbSNP153 33..33 33 - - - 59812 RMVar_ID_59812 Human_SNP_ID_464230202 m1A Human chr11 - 44066622 44066622 44066622 GCGGAAGCCGGGGTGGGAGTAAAGCCTGGGGTAGGGGGGCGGCGGGGTTCGAGCCTCCAGGCGTC GCGGAAGCCGGGGTGGGAGTAAAGCCTGGGGTTGGGGGGCGGCGGGGTTCGAGCCTCCAGGCGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:44066573..44066678 26863196 MeRIP-seq:(Medium) rs1410327279 Functional Loss SNV dbSNP153 33..33 33 - - - 59813 RMVar_ID_59813 Human_SNP_ID_464237532 m1A Human chr11 + 44095782 44095760 44095782 GCTGGCGATTCGGACCGATCCGACCTGGGCGGAGGTGGCCCGCGCCCCGCGGCATGAGCCGGTGA GCTGGCGATTC______________________GGTGGCCCGCGCCCCGCGGCATGAGCCGGTGA CGGACCGATCCGACCTGGGCGGA C EXT2 Ensembl:ENSG00000151348 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:44095733..44096242 26863196 MeRIP-seq:(Medium) rs1173593863 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_749959,Human_RBP_ID_807858,Human_RBP_ID_4183997,Human_RBP_ID_5314125,Human_RBP_ID_8940533,Human_RBP_ID_9321367,Human_RBP_ID_19697427,Human_RBP_ID_22433475,Human_RBP_ID_23505476 Human_Splice_Rec_1230767,Human_Splice_Rec_1230773,Human_Splice_Rec_1230799,Human_Splice_Rec_1230803 RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_149264 59814 RMVar_ID_59814 Human_SNP_ID_464237560 m1A Human chr11 + 44095851 44095851 44095851 GCTCGGGGCCGAGCGGGAGGCAGCCGTGGCCGAGGTAAGCGCGGCTCTCCAGGGCGGCGGCCGGG GCTCGGGGCCGAGCGGGAGGCAGCCGTGGCCGGGGTAAGCGCGGCTCTCCAGGGCGGCGGCCGGG A G EXT2 Ensembl:ENSG00000151348 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:44095801..44095875 32194978 MeRIP-seq:(Medium) rs1258303122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_749960,Human_RBP_ID_4183998,Human_RBP_ID_8940533,Human_RBP_ID_19697427,Human_RBP_ID_22433476 Human_Splice_Rec_1230767,Human_Splice_Rec_1230773,Human_Splice_Rec_1230799,Human_Splice_Rec_1230803 RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_149264 59815 RMVar_ID_59815 Human_SNP_ID_464237561 m1A Human chr11 + 44095851 44095851 44095851 GCTCGGGGCCGAGCGGGAGGCAGCCGTGGCCGAGGTAAGCGCGGCTCTCCAGGGCGGCGGCCGGG GCTCGGGGCCGAGCGGGAGGCAGCCGTGGCCGTGGTAAGCGCGGCTCTCCAGGGCGGCGGCCGGG A T EXT2 Ensembl:ENSG00000151348 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:44095801..44095875 32194978 MeRIP-seq:(Medium) rs1258303122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_749960,Human_RBP_ID_4183998,Human_RBP_ID_8940533,Human_RBP_ID_19697427,Human_RBP_ID_22433476 Human_Splice_Rec_1230767,Human_Splice_Rec_1230773,Human_Splice_Rec_1230799,Human_Splice_Rec_1230803 RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_149264 59816 RMVar_ID_59816 Human_SNP_ID_464237735 m1A Human chr11 + 44096336 44096335 44096336 CAGAAGCCGTGGGACGAGGTAGGGAAGGGGCCAGGGGCATGTTATGCCGGGGACTGGGTGGTCGG CAGAAGCCGTGGGACGAGGTAGGGAAGGGGCC_GGGGCATGTTATGCCGGGGACTGGGTGGTCGG CA C EXT2 Ensembl:ENSG00000151348 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:44096331..44096611 26863196 MeRIP-seq:(Medium) rs1218228586 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_149264 59817 RMVar_ID_59817 Human_SNP_ID_464237737 m1A Human chr11 + 44096336 44096336 44096336 CAGAAGCCGTGGGACGAGGTAGGGAAGGGGCCAGGGGCATGTTATGCCGGGGACTGGGTGGTCGG CAGAAGCCGTGGGACGAGGTAGGGAAGGGGCCGGGGGCATGTTATGCCGGGGACTGGGTGGTCGG A G EXT2 Ensembl:ENSG00000151348 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:44096331..44096611 26863196 MeRIP-seq:(Medium) rs1441575214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_149264 59818 RMVar_ID_59818 Human_SNP_ID_464237756 m1A Human chr11 - 44096365 44096365 44096365 GGTCACCCAGTCCCCGGCCTAACACGCCCCCGACCACCCAGTCCCCGGCATAACATGCCCCTGGC GGTCACCCAGTCCCCGGCCTAACACGCCCCCGGCCACCCAGTCCCCGGCATAACATGCCCCTGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:44096363..44096563 26863196 MeRIP-seq:(Medium) rs1432842366 Functional Loss SNV dbSNP153 33..33 33 - - - 59819 RMVar_ID_59819 Human_SNP_ID_464240282 m1A Human chr11 + 44107732 44107732 44107732 TGTCTGTGTCATTATGTGTGCGTCGGTCAAGTATAATATCCGGGGTCCTGCCCTCATCCCAAGAA TGTCTGTGTCATTATGTGTGCGTCGGTCAAGTGTAATATCCGGGGTCCTGCCCTCATCCCAAGAA A G EXT2 Ensembl:ENSG00000151348 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:44107656..44107749;chr11:44107659..44107775;chr11:44104779..44107800 26863196 MeRIP-seq:(Medium) rs765725291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396455,Human_RBP_ID_1162010,Human_RBP_ID_4184000,Human_RBP_ID_5138851,Human_RBP_ID_17796106,Human_RBP_ID_26803382 Human_Splice_Rec_1230772,Human_Splice_Rec_1230774,Human_Splice_Rec_1230802,Human_Splice_Rec_1230804,Human_Splice_Rec_1230830,Human_Splice_Rec_1230856 Human_miRNA_ID_166046,Human_miRNA_ID_1998270,Human_miRNA_ID_1998271,Human_miRNA_ID_2985402,Human_miRNA_ID_2985403 RMVar_hsa_circ_149266,RMVar_hsa_circ_287841,RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_290640,RMVar_hsa_circ_374519,RMVar_hsa_circ_149264,RMVar_hsa_circ_302663,RMVar_hsa_circ_289325,RMVar_hsa_circ_21418,RMVar_hsa_circ_273779,RMVar_hsa_circ_283335,RMVar_hsa_circ_273601,RMVar_hsa_circ_149268,RMVar_hsa_circ_149270,RMVar_hsa_circ_149271,RMVar_hsa_circ_149269,RMVar_hsa_circ_149267 59820 RMVar_ID_59820 Human_SNP_ID_464240463 m1A Human chr11 - 44108178 44108178 44108178 GCGCAGTGTGTTCTGGTTAAGCACATCGATGGAGGGAACAAACAGACAGGCCCGGTTGATGTCAT GCGCAGTGTGTTCTGGTTAAGCACATCGATGGCGGGAACAAACAGACAGGCCCGGTTGATGTCAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:44108127..44108228 32194978 MeRIP-seq:(Medium) rs1042043198 Functional Loss SNV dbSNP153 33..33 33 - - - 59821 RMVar_ID_59821 Human_SNP_ID_464241802 m1A Human chr11 + 44114299 44114299 44114299 TCAGCTGAGGTGGATCTTCCAGAGAAAGGACCAGGGTAAGGTACATTCATCCCAGCCAGGTGTGC TCAGCTGAGGTGGATCTTCCAGAGAAAGGACCGGGGTAAGGTACATTCATCCCAGCCAGGTGTGC A G EXT2 Ensembl:ENSG00000151348 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:44114251..44114347 32194978 MeRIP-seq:(Medium) rs773214800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940329,Human_RBP_ID_9343947,Human_RBP_ID_22753425 Human_Splice_Rec_1230779,Human_Splice_Rec_1230809,Human_Splice_Rec_1230835,Human_Splice_Rec_1230861,Human_Splice_Rec_1230885 RMVar_hsa_circ_149266,RMVar_hsa_circ_287841,RMVar_hsa_circ_97028,RMVar_hsa_circ_149263,RMVar_hsa_circ_113246,RMVar_hsa_circ_149265,RMVar_hsa_circ_79416,RMVar_hsa_circ_290640,RMVar_hsa_circ_374519,RMVar_hsa_circ_149264,RMVar_hsa_circ_302663,RMVar_hsa_circ_21418,RMVar_hsa_circ_273779,RMVar_hsa_circ_283335,RMVar_hsa_circ_273601,RMVar_hsa_circ_149268,RMVar_hsa_circ_149270,RMVar_hsa_circ_149269,RMVar_hsa_circ_149267,RMVar_hsa_circ_32794,RMVar_hsa_circ_98223,RMVar_hsa_circ_149272 59822 RMVar_ID_59822 Human_SNP_ID_464273903 m1A Human chr11 - 44261747 44261747 44261747 TAAGATCTCAACAGAGATGGCAACTTAAAAATAAAGTCGTGGGTAGCCGGCAGATGGATGGGCAG TAAGATCTCAACAGAGATGGCAACTTAAAAATGAAGTCGTGGGTAGCCGGCAGATGGATGGGCAG T C ALX4 Ensembl:ENSG00000052850 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4755239 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_200 GWAS_ID_6961,GWAS_ID_6962,GWAS_ID_6963,GWAS_ID_6964,GWAS_ID_6965,GWAS_ID_6966,GWAS_ID_6967,GWAS_ID_6968,GWAS_ID_6969,GWAS_ID_6970,GWAS_ID_6971,GWAS_ID_6972,GWAS_ID_6973,GWAS_ID_6974,GWAS_ID_6975,GWAS_ID_6976,GWAS_ID_6977,GWAS_ID_6978,GWAS_ID_6979,GWAS_ID_6980,GWAS_ID_6981,GWAS_ID_6982,GWAS_ID_6983,GWAS_ID_6984,GWAS_ID_6985,GWAS_ID_6986,GWAS_ID_6987,GWAS_ID_6988,GWAS_ID_6989,GWAS_ID_6990,GWAS_ID_6991,GWAS_ID_6992,GWAS_ID_6993,GWAS_ID_6994,GWAS_ID_6995,GWAS_ID_6996,GWAS_ID_6997,GWAS_ID_6998,GWAS_ID_6999,GWAS_ID_7000,GWAS_ID_7001,GWAS_ID_7002,GWAS_ID_7003,GWAS_ID_7004,GWAS_ID_7005,GWAS_ID_7006,GWAS_ID_7007,GWAS_ID_7008,GWAS_ID_7009,GWAS_ID_7010,GWAS_ID_7011,GWAS_ID_7012,GWAS_ID_7013,GWAS_ID_7014,GWAS_ID_7015,GWAS_ID_7016,GWAS_ID_7017,GWAS_ID_7018,GWAS_ID_7019,GWAS_ID_7020,GWAS_ID_7021,GWAS_ID_7022,GWAS_ID_7023,GWAS_ID_7024,GWAS_ID_7025,GWAS_ID_7026,GWAS_ID_7027,GWAS_ID_7028,GWAS_ID_7029,GWAS_ID_7030,GWAS_ID_7031,GWAS_ID_7032,GWAS_ID_7033,GWAS_ID_7034,GWAS_ID_7035,GWAS_ID_7036,GWAS_ID_7037,GWAS_ID_7038,GWAS_ID_7039,GWAS_ID_7040,GWAS_ID_7041,GWAS_ID_7042,GWAS_ID_7043,GWAS_ID_7044,GWAS_ID_7045,GWAS_ID_7046,GWAS_ID_7047,GWAS_ID_7048,GWAS_ID_7049,GWAS_ID_7050,GWAS_ID_7051,GWAS_ID_7052,GWAS_ID_7053 59823 RMVar_ID_59823 Human_SNP_ID_464362658 m1A Human chr11 - 44607953 44607953 44607953 GGGGTGTGGACTCTGAAGGGGAAGACAGGGGCAGGGGGTGCAATGCACAGAGCTTGGCTGGGGTC GGGGTGTGGACTCTGAAGGGGAAGACAGGGGCGGGGGGTGCAATGCACAGAGCTTGGCTGGGGTC T C AC010768.2 Ensembl:ENSG00000255092 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:44607952..44608061 26863196 MeRIP-seq:(Medium) rs1215276935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8064696 59824 RMVar_ID_59824 Human_SNP_ID_464443758 m1A Human chr11 + 44938312 44938312 44938312 ACGAGGTCCGTCTGGCTGTGCTTCTTCATCAGAGGCGGGGGCTGCTTGGCCGCCATCTTCTCCTC ACGAGGTCCGTCTGGCTGTGCTTCTTCATCAGCGGCGGGGGCTGCTTGGCCGCCATCTTCTCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:44938268..44938395 26863196 MeRIP-seq:(Medium) rs1472827352 Functional Loss SNV dbSNP153 33..33 33 - - - 59825 RMVar_ID_59825 Human_SNP_ID_464443784 m1A Human chr11 + 44938363 44938363 44938363 GCCATCTTCTCCTCCAGCCCGGCCTCTGCAGAAGGGCTGAGGGGAGACACCGGCCTCAGGCCACA GCCATCTTCTCCTCCAGCCCGGCCTCTGCAGACGGGCTGAGGGGAGACACCGGCCTCAGGCCACA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:44938315..44938416 32194978 MeRIP-seq:(Medium) rs753197355 Functional Loss SNV dbSNP153 33..33 33 - - - 59826 RMVar_ID_59826 Human_SNP_ID_464443785 m1A Human chr11 + 44938363 44938363 44938363 GCCATCTTCTCCTCCAGCCCGGCCTCTGCAGAAGGGCTGAGGGGAGACACCGGCCTCAGGCCACA GCCATCTTCTCCTCCAGCCCGGCCTCTGCAGAGGGGCTGAGGGGAGACACCGGCCTCAGGCCACA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:44938315..44938416 32194978 MeRIP-seq:(Medium) rs753197355 Functional Loss SNV dbSNP153 33..33 33 - - - 59827 RMVar_ID_59827 Human_SNP_ID_464444849 m1A Human chr11 + 44942123 44942109 44942124 CACACACCACACAATACGTGCACACACACGCCACACAAACCCACCACACATACATCACACACACC CACACACCACACAATACGT_______________ACAAACCCACCACACATACATCACACACACC TGCACACACACGCCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:44942119..44942221 26863196 MeRIP-seq:(Medium) rs1220008605 Functional Loss DEL dbSNP153 20..34 33 - - - 59828 RMVar_ID_59828 Human_SNP_ID_464447102 m1A Human chr11 + 44950630 44950630 44950630 TGGGTTGCGCTGCGCAGGCGGCGGGCGGCGGGAGGGGAAAGTCCGCGGCTCGGAAGCGGCGGCGG TGGGTTGCGCTGCGCAGGCGGCGGGCGGCGGGCGGGGAAAGTCCGCGGCTCGGAAGCGGCGGCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:44950629..44950871 26863196 MeRIP-seq:(Medium) rs1490092137 Functional Loss SNV dbSNP153 33..33 33 - - - 59829 RMVar_ID_59829 Human_SNP_ID_464447148 m1A Human chr11 - 44950763 44950763 44950763 GCCCTGCCCTGCCCTGCACTGCCCGGCCCGGCACGGGCGGCGCGATGTGAGGCGTCCGAGCCCGG GCCCTGCCCTGCCCTGCACTGCCCGGCCCGGCCCGGGCGGCGCGATGTGAGGCGTCCGAGCCCGG T G TP53I11 Ensembl:ENSG00000175274 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:44950722..44950894 26863196 MeRIP-seq:(Medium) rs1426767126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396610 Human_Splice_Rec_1231219,Human_Splice_Rec_1231277,Human_Splice_Rec_1231289,Human_Splice_Rec_1231301,Human_Splice_Rec_1231315,Human_Splice_Rec_1231321,Human_Splice_Rec_1231329,Human_Splice_Rec_1231341,Human_Splice_Rec_1231353,Human_Splice_Rec_1231359,Human_Splice_Rec_1231401 59830 RMVar_ID_59830 Human_SNP_ID_464498584 m1A Human chr11 - 45156872 45156872 45156872 TGCCTTTGCACATACTGTTCCCAGTGCCTAAAATGCCCTTCCCTCTCCCTCCGCCTGGCAAACCC TGCCTTTGCACATACTGTTCCCAGTGCCTAAAGTGCCCTTCCCTCTCCCTCCGCCTGGCAAACCC T C lnc-SYT13-2,lnc-SYT13-2:2,HSALNG0083916 RNACentral:URS00008C2C5D,RNACentral:URS00009B4C3B,RNACentral:URS0000EBE40D lincRNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:45156821..45157057 26863196 MeRIP-seq:(Medium) rs76851797 Functional Loss SNV dbSNP153 33..33 33 - - - 59831 RMVar_ID_59831 Human_SNP_ID_464504059 m1A Human chr11 + 45180797 45180797 45180797 CCCGCCCCGGCCGCAGCCTACACCGGCCCGAGACGGGGCGGCCACGGGGCAGGGGGCGGCGCGCC CCCGCCCCGGCCGCAGCCTACACCGGCCCGAGGCGGGGCGGCCACGGGGCAGGGGGCGGCGCGCC A G PRDM11 Ensembl:ENSG00000019485 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:45180747..45180869 26863196 MeRIP-seq:(Medium) rs984530066 Functional Loss SNV dbSNP153 33..33 33 - - - 59832 RMVar_ID_59832 Human_SNP_ID_464513112 m1A Human chr11 + 45219524 45219524 45219524 CCCAGCACTGTGCCGGCACCAGCGGGCACTCAACAAAGGGTGGCCCGTGCGTTCTCACCTGTCTC CCCAGCACTGTGCCGGCACCAGCGGGCACTCAGCAAAGGGTGGCCCGTGCGTTCTCACCTGTCTC A G PRDM11 Ensembl:ENSG00000019485 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:45219521..45219677 32194978 MeRIP-seq:(Medium) rs1482936084 Functional Loss SNV dbSNP153 33..33 33 - - - 59833 RMVar_ID_59833 Human_SNP_ID_464546112 m1A Human chr11 + 45356462 45356462 45356462 ATGGAATCTTCTTATTTGCTACACCTTTCACTACTGCTTGTGATATAGTGCAGGGTTGGGATGTG ATGGAATCTTCTTATTTGCTACACCTTTCACTGCTGCTTGTGATATAGTGCAGGGTTGGGATGTG A G LINC02696 Ensembl:ENSG00000254427 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58412666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23505845 Human_Splice_Rec_1231552,Human_Splice_Rec_1231560,Human_Splice_Rec_1231564 59834 RMVar_ID_59834 Human_SNP_ID_464656132 m1A Human chr11 - 45805312 45805312 45805312 AGGGGCGGGCAGGGGGAGGGAGGCGTACAGGGAGCTGCCGGAGGCCGGGCGCGGCTGGAGGGAGG AGGGGCGGGCAGGGGGAGGGAGGCGTACAGGGGGCTGCCGGAGGCCGGGCGCGGCTGGAGGGAGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:45805160..45805359 26863410 MeRIP-seq:(Medium) rs1363755032 Functional Loss SNV dbSNP153 33..33 33 - - - 59835 RMVar_ID_59835 Human_SNP_ID_464678701 m1A Human chr11 - 45900154 45900154 45900154 GGCTCCCCGCGCCGCCGCCGCCCGCAGAGAGCAGCCCGGCGCGCGGGGGCTGCACAGCGCACGGA GGCTCCCCGCGCCGCCGCCGCCCGCAGAGAGCGGCCCGGCGCGCGGGGGCTGCACAGCGCACGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:45900130..45900210 26863196 MeRIP-seq:(Medium) rs1478805840 Functional Loss SNV dbSNP153 33..33 33 - - - 59836 RMVar_ID_59836 Human_SNP_ID_464678704 m1A Human chr11 - 45900157 45900157 45900157 ACCGGCTCCCCGCGCCGCCGCCGCCCGCAGAGAGCAGCCCGGCGCGCGGGGGCTGCACAGCGCAC ACCGGCTCCCCGCGCCGCCGCCGCCCGCAGAGGGCAGCCCGGCGCGCGGGGGCTGCACAGCGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:45900126..45900197 26863196 MeRIP-seq:(Medium) rs937016000 Functional Loss SNV dbSNP153 33..33 33 - - - 59837 RMVar_ID_59837 Human_SNP_ID_464679626 m1A Human chr11 - 45902948 45902948 45902948 CACTGTAGTCTCCGAAGCACGGCCGCAGGCTCACCAGCTCCAGCTGTGCATGCTCATCTACCACC CACTGTAGTCTCCGAAGCACGGCCGCAGGCTCGCCAGCTCCAGCTGTGCATGCTCATCTACCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:45902498..45902948 32194978 MeRIP-seq:(Medium) rs1207275995 Functional Loss SNV dbSNP153 33..33 33 - - - 59838 RMVar_ID_59838 Human_SNP_ID_464683234 m1A Human chr11 - 45914230 45914230 45914230 GGGGAGTGTGCTGAGCAAGGCCCCTGTGCTGGAGACATCCTTGACGCCTTGGCCGTCAGTGCTCA GGGGAGTGTGCTGAGCAAGGCCCCTGTGCTGGGGACATCCTTGACGCCTTGGCCGTCAGTGCTCA T C PEX16 Ensembl:ENSG00000121680 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:45914221..45914310 26863196 MeRIP-seq:(Medium) rs774876161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865761,Human_RBP_ID_5343494,Human_RBP_ID_18971825,Human_RBP_ID_22642286 Human_Splice_Rec_1232259,Human_Splice_Rec_1232279,Human_Splice_Rec_1232303,Human_Splice_Rec_1232317 RMVar_hsa_circ_322797,RMVar_hsa_circ_149307,RMVar_hsa_circ_100774,RMVar_hsa_circ_149306 59839 RMVar_ID_59839 Human_SNP_ID_464685831 m1A Human chr11 + 45923121 45923121 45923121 CGGAGACCCGGGGGCCGGCCCCGGGGACCACAACCGCTCCGACTGCGGCCCGCAGCCGCCGCCGC CGGAGACCCGGGGGCCGGCCCCGGGGACCACAGCCGCTCCGACTGCGGCCCGCAGCCGCCGCCGC A G LARGE2 Ensembl:ENSG00000165905 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:45922815..45923162 26863410 MeRIP-seq:(Medium) rs1382467190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1232374,Human_Splice_Rec_1232375,Human_Splice_Rec_1232397,Human_Splice_Rec_1232421,Human_Splice_Rec_1232443 59840 RMVar_ID_59840 Human_SNP_ID_464689298 m1A Human chr11 - 45933966 45933966 45933966 GAACTGTAACCAGGGGGAAGAGACTAAATAACAGAGCCCCTCTAGGAGAAGCCACGGGATCCCGG GAACTGTAACCAGGGGGAAGAGACTAAATAACGGAGCCCCTCTAGGAGAAGCCACGGGATCCCGG T C PHF21A Ensembl:ENSG00000135365 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:45933915..45934042 26863196 MeRIP-seq:(Medium) rs767435299 Functional Loss SNV dbSNP153 33..33 33 - - - 59841 RMVar_ID_59841 Human_SNP_ID_464696677 m1A Human chr11 + 45965427 45965427 45965427 TGGTGAGCTGGGCCATGGGGAACGTTTTGGCTATGGTTGCAGTCTGCCCATTGACGACACGGACG TGGTGAGCTGGGCCATGGGGAACGTTTTGGCTGTGGTTGCAGTCTGCCCATTGACGACACGGACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:45965376..45965565 26863196 MeRIP-seq:(Medium) rs1275678984 Functional Loss SNV dbSNP153 33..33 33 - - - 59842 RMVar_ID_59842 Human_SNP_ID_464697693 m1A Human chr11 + 45969843 45969843 45969843 TCACCTGTGGAAGAAAGTTTGGACGTGGAGTGAGTCTAGGAGGGGGGATAAACTGTGGTACTTTG TCACCTGTGGAAGAAAGTTTGGACGTGGAGTGGGTCTAGGAGGGGGGATAAACTGTGGTACTTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:45969773..45969842 26863196 MeRIP-seq:(Medium) rs1278674686 Functional Loss SNV dbSNP153 33..33 33 - - - 59843 RMVar_ID_59843 Human_SNP_ID_464700051 m1A Human chr11 - 45979883 45979883 45979883 CCGGACAAGTTCCAAATACAGCCATTGCCACAATCTGAAAACAAACTACAAACAGCACAGCAGCA CCGGACAAGTTCCAAATACAGCCATTGCCACAGTCTGAAAACAAACTACAAACAGCACAGCAGCA T C PHF21A Ensembl:ENSG00000135365 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:45979832..45979910 26863196 MeRIP-seq:(Medium) rs780039605 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_869680 Human_Splice_Rec_1232538,Human_Splice_Rec_1232580,Human_Splice_Rec_1232652,Human_Splice_Rec_1232656,Human_Splice_Rec_1232668,Human_Splice_Rec_1232678,Human_Splice_Rec_1232688,Human_Splice_Rec_1232702 RMVar_hsa_circ_113581,RMVar_hsa_circ_149313,RMVar_hsa_circ_36023,RMVar_hsa_circ_149315,RMVar_hsa_circ_109827,RMVar_hsa_circ_60454,RMVar_hsa_circ_355906,RMVar_hsa_circ_149316,RMVar_hsa_circ_25414,RMVar_hsa_circ_303931 59844 RMVar_ID_59844 Human_SNP_ID_464730798 m1A Human chr11 + 46120401 46120398 46120402 GGCGAGGCTCCGTGCCCCCCGCCCCCGCCCGCAGCCCCCGGCCGGCCCCCCGCCGGGACAATGTG GGCGAGGCTCCGTGCCCCCCGCCCCCGCCC____CCCCCGGCCGGCCCCCCGCCGGGACAATGTG CGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46120395..46120508 26863196 MeRIP-seq:(Medium) rs1328254697 Functional Loss DEL dbSNP153 31..34 33 - - - 59845 RMVar_ID_59845 Human_SNP_ID_464730802 m1A Human chr11 + 46120401 46120401 46120401 GGCGAGGCTCCGTGCCCCCCGCCCCCGCCCGCAGCCCCCGGCCGGCCCCCCGCCGGGACAATGTG GGCGAGGCTCCGTGCCCCCCGCCCCCGCCCGCCGCCCCCGGCCGGCCCCCCGCCGGGACAATGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46120395..46120508 26863196 MeRIP-seq:(Medium) rs1282433897 Functional Loss SNV dbSNP153 33..33 33 - - - 59846 RMVar_ID_59846 Human_SNP_ID_464731416 m1A Human chr11 + 46122012 46121986 46122012 GGCGGCGGCGGCGGTGATGGGGCCGAGCACCGAGCGGCGGCGAAGGCAGCCAAACTCCGGGGCCC GGCGGCG__________________________GCGGCGGCGAAGGCAGCCAAACTCCGGGGCCC GGCGGCGGTGATGGGGCCGAGCACCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46121964..46122112 26863196 MeRIP-seq:(Medium) rs947267764 Functional Loss DEL dbSNP153 8..33 33 - - - 59847 RMVar_ID_59847 Human_SNP_ID_464785963 m1A Human chr11 + 46347516 46347516 46347516 GGCAGCGGCTTCCCGGGCACCTGGGCGTGGGGAGCGGGGGCGCGCGGCGCGGGGCGGGCGGAGCG GGCAGCGGCTTCCCGGGCACCTGGGCGTGGGGGGCGGGGGCGCGCGGCGCGGGGCGGGCGGAGCG A G DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:46347476..46347733;chr11:46347476..46347737 26863196 MeRIP-seq:(Medium) rs1047784371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184010,Human_RBP_ID_5086764,Human_RBP_ID_8174170,Human_RBP_ID_18416811 59848 RMVar_ID_59848 Human_SNP_ID_464785996 m1A Human chr11 + 46347581 46347581 46347581 AGCGCGCGCCATGGAGGTGGCGGGCGGCGCGGAGCGGGCGTGCTGAGCCCCGGCCGCCGGCCCGG AGCGCGCGCCATGGAGGTGGCGGGCGGCGCGGGGCGGGCGTGCTGAGCCCCGGCCGCCGGCCCGG A G DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:46347498..46347580 26863410 MeRIP-seq:(Medium) rs1375507197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751274,Human_RBP_ID_4184010,Human_RBP_ID_5086764,Human_RBP_ID_5313586,Human_RBP_ID_8174170,Human_RBP_ID_9321368,Human_RBP_ID_18416811,Human_RBP_ID_18477650 59849 RMVar_ID_59849 Human_SNP_ID_464790589 m1A Human chr11 + 46365280 46365280 46365280 GCTTCCAGCATCAGGGCCGCAGAAGAATGTGCAGTCACAGGCTCCATCAGGAGCAGAGTCAGAAG GCTTCCAGCATCAGGGCCGCAGAAGAATGTGCGGTCACAGGCTCCATCAGGAGCAGAGTCAGAAG A G DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46365124..46365382 26863196 MeRIP-seq:(Medium) rs1336810609 Functional Loss SNV dbSNP153 33..33 33 - - - 59850 RMVar_ID_59850 Human_SNP_ID_464791370 m1A Human chr11 + 46367320 46367320 46367320 TAGGAAAGCCATCACCAAGTCGGGCCTCCAGCACCTGGCCCCCCCTCCGCCCACCCCTGGGGCCC TAGGAAAGCCATCACCAAGTCGGGCCTCCAGCGCCTGGCCCCCCCTCCGCCCACCCCTGGGGCCC A G DGKZ Ensembl:ENSG00000149091 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:46367289..46367415 26863196 MeRIP-seq:(Medium) rs759956247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870154,Human_RBP_ID_3939036,Human_RBP_ID_8773411,Human_RBP_ID_22642943 Human_Splice_Rec_1232852,Human_Splice_Rec_1232853,Human_Splice_Rec_1232912,Human_Splice_Rec_1232913,Human_Splice_Rec_1232918,Human_Splice_Rec_1232919,Human_Splice_Rec_1233032,Human_Splice_Rec_1233033,Human_Splice_Rec_1233082,Human_Splice_Rec_1233083,Human_Splice_Rec_1233086,Human_Splice_Rec_1233087,Human_Splice_Rec_1233146,Human_Splice_Rec_1233147,Human_Splice_Rec_1233212,Human_Splice_Rec_1233213,Human_Splice_Rec_1233272,Human_Splice_Rec_1233273,Human_Splice_Rec_1233332,Human_Splice_Rec_1233333,Human_Splice_Rec_1233392,Human_Splice_Rec_1233393,Human_Splice_Rec_1233398,Human_Splice_Rec_1233399,Human_Splice_Rec_1233458,Human_Splice_Rec_1233459,Human_Splice_Rec_1233463 RMVar_hsa_circ_149329,RMVar_hsa_circ_273489,RMVar_hsa_circ_333027,RMVar_hsa_circ_50019,RMVar_hsa_circ_149328 59851 RMVar_ID_59851 Human_SNP_ID_464791386 m1A Human chr11 + 46367340 46367340 46367340 CGGGCCTCCAGCACCTGGCCCCCCCTCCGCCCACCCCTGGGGCCCCGTGCAGCGAGTCAGAGCGG CGGGCCTCCAGCACCTGGCCCCCCCTCCGCCCCCCCCTGGGGCCCCGTGCAGCGAGTCAGAGCGG A C DGKZ Ensembl:ENSG00000149091 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:46367276..46367438;chr11:46367287..46367435 26863196 MeRIP-seq:(Medium) rs772181855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3939036,Human_RBP_ID_8773411,Human_RBP_ID_17796293 Human_Splice_Rec_1232852,Human_Splice_Rec_1232853,Human_Splice_Rec_1232912,Human_Splice_Rec_1232913,Human_Splice_Rec_1232918,Human_Splice_Rec_1232919,Human_Splice_Rec_1233032,Human_Splice_Rec_1233033,Human_Splice_Rec_1233082,Human_Splice_Rec_1233083,Human_Splice_Rec_1233086,Human_Splice_Rec_1233087,Human_Splice_Rec_1233146,Human_Splice_Rec_1233147,Human_Splice_Rec_1233212,Human_Splice_Rec_1233213,Human_Splice_Rec_1233272,Human_Splice_Rec_1233273,Human_Splice_Rec_1233332,Human_Splice_Rec_1233333,Human_Splice_Rec_1233392,Human_Splice_Rec_1233393,Human_Splice_Rec_1233398,Human_Splice_Rec_1233399,Human_Splice_Rec_1233458,Human_Splice_Rec_1233459,Human_Splice_Rec_1233463 RMVar_hsa_circ_149329,RMVar_hsa_circ_273489,RMVar_hsa_circ_333027,RMVar_hsa_circ_50019,RMVar_hsa_circ_149328 59852 RMVar_ID_59852 Human_SNP_ID_464791389 m1A Human chr11 - 46367345 46367344 46367345 ATCTGCCGCTCTGACTCGCTGCACGGGGCCCCAGGGGTGGGCGGAGGGGGGGCCAGGTGCTGGAG ATCTGCCGCTCTGACTCGCTGCACGGGGCCCC_GGGGTGGGCGGAGGGGGGGCCAGGTGCTGGAG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46367300..46367436 26863196 MeRIP-seq:(Medium) rs1041225858 Functional Loss DEL dbSNP153 33..33 33 - - - 59853 RMVar_ID_59853 Human_SNP_ID_464791473 m1A Human chr11 + 46367601 46367601 46367601 TGGGAGAGGGCGGGTGGGCGGGGGCTGATGGGAGGGAGGGCTGGGCGGCCAGCGTGTGCTGAGCA TGGGAGAGGGCGGGTGGGCGGGGGCTGATGGGGGGGAGGGCTGGGCGGCCAGCGTGTGCTGAGCA A G DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46367600..46367672 26863196 MeRIP-seq:(Medium) rs922124630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5341258,Human_RBP_ID_8174177,Human_RBP_ID_9321369,Human_RBP_ID_9414484 RMVar_hsa_circ_149329,RMVar_hsa_circ_273489,RMVar_hsa_circ_333027,RMVar_hsa_circ_50019,RMVar_hsa_circ_149328 59854 RMVar_ID_59854 Human_SNP_ID_464794759 m1A Human chr11 - 46377249 46377249 46377249 TTCAGAAGTCATCGGCTTACAGGTGGGGCTGAAAGCCAGGGGCTGGAGGGACGGGACACCAGGAC TTCAGAAGTCATCGGCTTACAGGTGGGGCTGATAGCCAGGGGCTGGAGGGACGGGACACCAGGAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46377198..46377621 26863196 MeRIP-seq:(Medium) rs776402993 Functional Loss SNV dbSNP153 33..33 33 - - - 59855 RMVar_ID_59855 Human_SNP_ID_464794852 m1A Human chr11 - 46377583 46377583 46377583 TGGTATGCTCTGCATTTTTAGTTGACCGTGGTATGGAGATGGGGGTTCGAGGGCACGAATGGCCA TGGTATGCTCTGCATTTTTAGTTGACCGTGGTTTGGAGATGGGGGTTCGAGGGCACGAATGGCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46377187..46377837 26863196 MeRIP-seq:(Medium) rs1199009540 Functional Loss SNV dbSNP153 33..33 33 - - - 59856 RMVar_ID_59856 Human_SNP_ID_464796709 m1A Human chr11 - 46382598 46382598 46382598 CCCATCACACGCACCCCAGTTCTCAAACTTGTACTTGCAGTCGGCTGGCGAGAGAGCGGCCCAGG CCCATCACACGCACCCCAGTTCTCAAACTTGTGCTTGCAGTCGGCTGGCGAGAGAGCGGCCCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:46382051..46382814 32194978 MeRIP-seq:(Medium) rs745326945 Functional Loss SNV dbSNP153 33..33 33 - - - 59857 RMVar_ID_59857 Human_SNP_ID_464797107 m1A Human chr11 - 46383556 46383550 46383556 GGCACTGGTGGGTCACATCTCGGGCCTGGGAGAGGGAGGGCGTGGGCCAGGCCCCATGTGACACC GGCACTGGTGGGTCACATCTCGGGCCTGGGAG______GGCGTGGGCCAGGCCCCATGTGACACC CCTCCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46383512..46383753 26863196 MeRIP-seq:(Medium) rs1289934365 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_149334 59858 RMVar_ID_59858 Human_SNP_ID_464797139 m1A Human chr11 + 46383618 46383618 46383618 GCCTTCTGTCTGCTCGTTAGCTTTAATCAATCATGCCCTGCCTTGTCCCTCTCACTCCCCAGCCC GCCTTCTGTCTGCTCGTTAGCTTTAATCAATCGTGCCCTGCCTTGTCCCTCTCACTCCCCAGCCC A G MDK Ensembl:ENSG00000110492 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46383492..46383637 26863196 MeRIP-seq:(Medium) rs1387017465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396754,Human_RBP_ID_4190479,Human_RBP_ID_5110386,Human_RBP_ID_5138526,Human_RBP_ID_17074128,Human_RBP_ID_17649050,Human_RBP_ID_18932351,Human_RBP_ID_23506357,Human_RBP_ID_24459915,Human_RBP_ID_24886201,Human_RBP_ID_26403868,Human_RBP_ID_26890733,Human_RBP_ID_27201626 Human_miRNA_ID_1015326,Human_miRNA_ID_1061442,Human_miRNA_ID_1193474,Human_miRNA_ID_1372612 RMVar_hsa_circ_266875 59859 RMVar_ID_59859 Human_SNP_ID_464797150 m1A Human chr11 + 46383639 46383639 46383639 TTTAATCAATCATGCCCTGCCTTGTCCCTCTCACTCCCCAGCCCCACCCCTAAGTGCCCAAAGTG TTTAATCAATCATGCCCTGCCTTGTCCCTCTCGCTCCCCAGCCCCACCCCTAAGTGCCCAAAGTG A G MDK Ensembl:ENSG00000110492 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:46383538..46383747 26863410 MeRIP-seq:(Medium) rs1225656729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227573,Human_RBP_ID_396754,Human_RBP_ID_750987,Human_RBP_ID_5110386,Human_RBP_ID_5138526,Human_RBP_ID_6075563,Human_RBP_ID_17074128,Human_RBP_ID_17649050,Human_RBP_ID_18932351,Human_RBP_ID_27201626,Human_RBP_ID_27411666 Human_miRNA_ID_94668,Human_miRNA_ID_866573 RMVar_hsa_circ_266875 59860 RMVar_ID_59860 Human_SNP_ID_464800736 m1A Human chr11 + 46396827 46396827 46396827 CTCCTGAGTGAGGACCTGCCCACTGTCCCTTGACCCCATCCTGTATCAGGCAAGCAGGCGCCCCC CTCCTGAGTGAGGACCTGCCCACTGTCCCTTGTCCCCATCCTGTATCAGGCAAGCAGGCGCCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46396777..46396892 26863196 MeRIP-seq:(Medium) rs1045614166 Functional Loss SNV dbSNP153 33..33 33 - - - 59861 RMVar_ID_59861 Human_SNP_ID_464800866 m1A Human chr11 - 46397294 46397294 46397294 GTCAGGGTGGAGAGGAAGATCAGTCAGTGGGCACAAGACAGTCAAATGGGCAAGGCCTGCCTCGG GTCAGGGTGGAGAGGAAGATCAGTCAGTGGGCCCAAGACAGTCAAATGGGCAAGGCCTGCCTCGG T G AMBRA1 Ensembl:ENSG00000110497 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46397243..46397379 26863196 MeRIP-seq:(Medium) rs1210980020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8229343,Human_RBP_ID_11624021,Human_RBP_ID_26408380 59862 RMVar_ID_59862 Human_SNP_ID_464801002 m1A Human chr11 - 46397622 46397622 46397622 TTCCTGGGACCAGCCTGGTACCCCTGGGCGGGAGCCAACCCAGCCAACCCTGCCCTCTTCCTCCC TTCCTGGGACCAGCCTGGTACCCCTGGGCGGGGGCCAACCCAGCCAACCCTGCCCTCTTCCTCCC T C AMBRA1 Ensembl:ENSG00000110497 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:46397577..46397693 26863196 MeRIP-seq:(Medium) rs1369675167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18933443 59863 RMVar_ID_59863 Human_SNP_ID_464808561 m1A Human chr11 - 46428763 46428763 46428763 GAGGGGAAGCTGACAGAGATACCTACAGACGGAGTGCTGTGCCACCTGGTGCCGACAAGAAAGCC GAGGGGAAGCTGACAGAGATACCTACAGACGGTGTGCTGTGCCACCTGGTGCCGACAAGAAAGCC T A AMBRA1,AC024293.1 Ensembl:ENSG00000110497,Ensembl:ENSG00000244313 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1310538621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29174,Human_RBP_ID_396768,Human_RBP_ID_748713,Human_RBP_ID_869080,Human_RBP_ID_987172,Human_RBP_ID_1063904,Human_RBP_ID_1126543,Human_RBP_ID_1457021,Human_RBP_ID_1779411,Human_RBP_ID_3375457,Human_RBP_ID_5093001,Human_RBP_ID_5110740,Human_RBP_ID_5169027,Human_RBP_ID_5640894,Human_RBP_ID_5644290,Human_RBP_ID_6075600,Human_RBP_ID_8176865,Human_RBP_ID_8247104,Human_RBP_ID_8351810,Human_RBP_ID_8774622,Human_RBP_ID_9003999,Human_RBP_ID_9254911,Human_RBP_ID_9321374,Human_RBP_ID_9415746,Human_RBP_ID_9654095,Human_RBP_ID_11624335,Human_RBP_ID_17185348,Human_RBP_ID_17467244,Human_RBP_ID_17560774,Human_RBP_ID_17581531,Human_RBP_ID_17648660,Human_RBP_ID_17667639,Human_RBP_ID_17673000,Human_RBP_ID_17682974,Human_RBP_ID_17804537,Human_RBP_ID_18409241,Human_RBP_ID_18478841,Human_RBP_ID_18510908,Human_RBP_ID_18608039,Human_RBP_ID_18926285,Human_RBP_ID_19055646,Human_RBP_ID_19697739,Human_RBP_ID_21959515,Human_RBP_ID_22369740,Human_RBP_ID_22425412,Human_RBP_ID_23207267,Human_RBP_ID_23506380,Human_RBP_ID_26804589 RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341 59864 RMVar_ID_59864 Human_SNP_ID_464808566 m1A Human chr11 - 46428777 46428777 46428777 TGCGAGACTCACAAGAGGGGAAGCTGACAGAGATACCTACAGACGGAGTGCTGTGCCACCTGGTG TGCGAGACTCACAAGAGGGGAAGCTGACAGAGGTACCTACAGACGGAGTGCTGTGCCACCTGGTG T C AMBRA1,AC024293.1 Ensembl:ENSG00000110497,Ensembl:ENSG00000244313 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs14196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29174,Human_RBP_ID_396768,Human_RBP_ID_748713,Human_RBP_ID_869080,Human_RBP_ID_1063904,Human_RBP_ID_1457021,Human_RBP_ID_1779411,Human_RBP_ID_5093001,Human_RBP_ID_5110740,Human_RBP_ID_5644290,Human_RBP_ID_6075600,Human_RBP_ID_9003999,Human_RBP_ID_9254911,Human_RBP_ID_9321374,Human_RBP_ID_9654095,Human_RBP_ID_17185348,Human_RBP_ID_17351027,Human_RBP_ID_17560774,Human_RBP_ID_17581531,Human_RBP_ID_17648660,Human_RBP_ID_17667639,Human_RBP_ID_17673000,Human_RBP_ID_17682974,Human_RBP_ID_17804537,Human_RBP_ID_18409241,Human_RBP_ID_18478841,Human_RBP_ID_18608039,Human_RBP_ID_19055646,Human_RBP_ID_19697739,Human_RBP_ID_21959515,Human_RBP_ID_22425412,Human_RBP_ID_23207267,Human_RBP_ID_26804590 RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341 59865 RMVar_ID_59865 Human_SNP_ID_464808574 m1A Human chr11 - 46428803 46428803 46428803 CCTAAAGGTCTGGAGGGTGAGCGACCTGCGAGACTCACAAGAGGGGAAGCTGACAGAGATACCTA CCTAAAGGTCTGGAGGGTGAGCGACCTGCGAGTCTCACAAGAGGGGAAGCTGACAGAGATACCTA T A AMBRA1,AC024293.1 Ensembl:ENSG00000110497,Ensembl:ENSG00000244313 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1014053796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_396773,Human_RBP_ID_1063904,Human_RBP_ID_1779413,Human_RBP_ID_3375459,Human_RBP_ID_4190490,Human_RBP_ID_6075602,Human_RBP_ID_8351811,Human_RBP_ID_17351141,Human_RBP_ID_17681977,Human_RBP_ID_26403876,Human_RBP_ID_26890748 Human_miRNA_ID_1898924 RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341 59866 RMVar_ID_59866 Human_SNP_ID_464808656 m1A Human chr11 - 46429036 46429036 46429036 ACATGCCTAAGCACCCGGAGCTGGCAGACAAGAATGTGCCCAACCTTCATGTCATGAAGGCCATG ACATGCCTAAGCACCCGGAGCTGGCAGACAAGCATGTGCCCAACCTTCATGTCATGAAGGCCATG T G AMBRA1,AC024293.1 Ensembl:ENSG00000110497,Ensembl:ENSG00000244313 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs577136518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341 59867 RMVar_ID_59867 Human_SNP_ID_464809653 m1A Human chr11 - 46433622 46433622 46433622 TATTTCTCTGTTTTGTTGGCCCTCAGGTCCCAATGCCATTTCGGTGAGCCTGTCCCCAATGGGCA TATTTCTCTGTTTTGTTGGCCCTCAGGTCCCAGTGCCATTTCGGTGAGCCTGTCCCCAATGGGCA T C AMBRA1 Ensembl:ENSG00000110497 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs552593017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865766,Human_RBP_ID_22641078,Human_RBP_ID_24557182,Human_RBP_ID_24912277 Human_Splice_Rec_1233670,Human_Splice_Rec_1233704,Human_Splice_Rec_1233736,Human_Splice_Rec_1233770,Human_Splice_Rec_1233806 RMVar_hsa_circ_25772,RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_293057,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341,RMVar_hsa_circ_339423,RMVar_hsa_circ_372836,RMVar_hsa_circ_282599,RMVar_hsa_circ_284275,RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_149344,RMVar_hsa_circ_149346,RMVar_hsa_circ_149347,RMVar_hsa_circ_149345,RMVar_hsa_circ_149343 59868 RMVar_ID_59868 Human_SNP_ID_464809654 m1A Human chr11 - 46433622 46433622 46433622 TATTTCTCTGTTTTGTTGGCCCTCAGGTCCCAATGCCATTTCGGTGAGCCTGTCCCCAATGGGCA TATTTCTCTGTTTTGTTGGCCCTCAGGTCCCACTGCCATTTCGGTGAGCCTGTCCCCAATGGGCA T G AMBRA1 Ensembl:ENSG00000110497 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs552593017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865766,Human_RBP_ID_22641078,Human_RBP_ID_24557182,Human_RBP_ID_24912277 Human_Splice_Rec_1233670,Human_Splice_Rec_1233704,Human_Splice_Rec_1233736,Human_Splice_Rec_1233770,Human_Splice_Rec_1233806 RMVar_hsa_circ_25772,RMVar_hsa_circ_25905,RMVar_hsa_circ_269632,RMVar_hsa_circ_24443,RMVar_hsa_circ_149337,RMVar_hsa_circ_149335,RMVar_hsa_circ_298103,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_313818,RMVar_hsa_circ_326618,RMVar_hsa_circ_294536,RMVar_hsa_circ_26810,RMVar_hsa_circ_293057,RMVar_hsa_circ_149339,RMVar_hsa_circ_149340,RMVar_hsa_circ_149341,RMVar_hsa_circ_339423,RMVar_hsa_circ_372836,RMVar_hsa_circ_282599,RMVar_hsa_circ_284275,RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_149344,RMVar_hsa_circ_149346,RMVar_hsa_circ_149347,RMVar_hsa_circ_149345,RMVar_hsa_circ_149343 59869 RMVar_ID_59869 Human_SNP_ID_464854783 m1A Human chr11 + 46617603 46617603 46617603 TGAAAACAAACACTAACGATGGCGGCGCCGGGAAGCGACCGGCTGCTGGGCTTAAGGCGGGAGTG TGAAAACAAACACTAACGATGGCGGCGCCGGGGAGCGACCGGCTGCTGGGCTTAAGGCGGGAGTG A G ATG13 Ensembl:ENSG00000175224 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46617551..46617777 26863196 MeRIP-seq:(Medium) rs540059893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807759,Human_RBP_ID_4185729,Human_RBP_ID_22432867 RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 59870 RMVar_ID_59870 Human_SNP_ID_464871400 m1A Human chr11 - 46678274 46678274 46678274 CCTCCCTCTCCACCTCCCCGCCCCCGAGAGCTACAGCGTGTGATGGAATCAGTGACCGGCCAGGT CCTCCCTCTCCACCTCCCCGCCCCCGAGAGCTGCAGCGTGTGATGGAATCAGTGACCGGCCAGGT T C ARHGAP1 Ensembl:ENSG00000175220 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:46678226..46678300 26863196 MeRIP-seq:(Medium) rs922398460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8175701,Human_RBP_ID_18932356 RMVar_hsa_circ_99639,RMVar_hsa_circ_120451,RMVar_hsa_circ_106926,RMVar_hsa_circ_110491,RMVar_hsa_circ_103461,RMVar_hsa_circ_149391,RMVar_hsa_circ_149395,RMVar_hsa_circ_88100,RMVar_hsa_circ_97086,RMVar_hsa_circ_149397,RMVar_hsa_circ_87347,RMVar_hsa_circ_149396,RMVar_hsa_circ_149393,RMVar_hsa_circ_149394,RMVar_hsa_circ_149392,RMVar_hsa_circ_149390 59871 RMVar_ID_59871 Human_SNP_ID_464876832 m1A Human chr11 - 46700441 46700440 46700441 GGGTCCGGATGGGGAGGACCGGAGCAGATCCGAGGAGGGGAACGGGGGTGGAACTGGGCTCAGAG GGGTCCGGATGGGGAGGACCGGAGCAGATCCG_GGAGGGGAACGGGGGTGGAACTGGGCTCAGAG CT C ARHGAP1 Ensembl:ENSG00000175220 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46700425..46700557 26863196 MeRIP-seq:(Medium) rs963588807 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_808356,Human_RBP_ID_869200,Human_RBP_ID_5341271 RMVar_hsa_circ_120451,RMVar_hsa_circ_149397,RMVar_hsa_circ_118713,RMVar_hsa_circ_149399,RMVar_hsa_circ_120970,RMVar_hsa_circ_149403 59872 RMVar_ID_59872 Human_SNP_ID_464876833 m1A Human chr11 - 46700441 46700441 46700441 GGGTCCGGATGGGGAGGACCGGAGCAGATCCGAGGAGGGGAACGGGGGTGGAACTGGGCTCAGAG GGGTCCGGATGGGGAGGACCGGAGCAGATCCGCGGAGGGGAACGGGGGTGGAACTGGGCTCAGAG T G ARHGAP1 Ensembl:ENSG00000175220 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46700425..46700557 26863196 MeRIP-seq:(Medium) rs1291773558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808356,Human_RBP_ID_869200,Human_RBP_ID_5341271 RMVar_hsa_circ_120451,RMVar_hsa_circ_149397,RMVar_hsa_circ_118713,RMVar_hsa_circ_149399,RMVar_hsa_circ_120970,RMVar_hsa_circ_149403 59873 RMVar_ID_59873 Human_SNP_ID_464891648 m1A Human chr11 - 46755018 46755018 46755018 ACAGGAAGACAAAGCTGAAGCCATGTCCGGCCATATTGATCAGTTTCTGATAGCCACTTTTATGC ACAGGAAGACAAAGCTGAAGCCATGTCCGGCCGTATTGATCAGTTTCTGATAGCCACTTTTATGC T C CKAP5 Ensembl:ENSG00000175216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46754967..46755088 26863196 MeRIP-seq:(Medium) rs779274910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8769527 Human_Splice_Rec_1234470,Human_Splice_Rec_1234672,Human_Splice_Rec_1234714 Human_miRNA_ID_2212499,Human_miRNA_ID_2471195 RMVar_hsa_circ_1052,RMVar_hsa_circ_149412,RMVar_hsa_circ_149411,RMVar_hsa_circ_108805,RMVar_hsa_circ_331768,RMVar_hsa_circ_68016,RMVar_hsa_circ_118161,RMVar_hsa_circ_108038,RMVar_hsa_circ_149415,RMVar_hsa_circ_4038,RMVar_hsa_circ_79766,RMVar_hsa_circ_101169,RMVar_hsa_circ_149416,RMVar_hsa_circ_149418,RMVar_hsa_circ_149420,RMVar_hsa_circ_24301,RMVar_hsa_circ_324685,RMVar_hsa_circ_375595,RMVar_hsa_circ_305514,RMVar_hsa_circ_149421,RMVar_hsa_circ_149419,RMVar_hsa_circ_23336,RMVar_hsa_circ_268873,RMVar_hsa_circ_288220,RMVar_hsa_circ_149422,RMVar_hsa_circ_278575,RMVar_hsa_circ_35256,RMVar_hsa_circ_16171,RMVar_hsa_circ_149423,RMVar_hsa_circ_149424 59874 RMVar_ID_59874 Human_SNP_ID_464892557 m1A Human chr11 + 46758890 46758890 46758890 ATTCATCACATTTATAGCCTCTATGTCCACCAATGGAATCCCTGTCACGGGAGCACACCCATTAC ATTCATCACATTTATAGCCTCTATGTCCACCAGTGGAATCCCTGTCACGGGAGCACACCCATTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46758888..46758986 26863196 MeRIP-seq:(Medium) rs114083473 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7054 59875 RMVar_ID_59875 Human_SNP_ID_464892652 m1A Human chr11 + 46759254 46759252 46759254 CTGATCATCATGAACTGCTCATATTTAAATGAAAGAGTTTAACTCACTTGGGTTCAGGAATAAGG CTGATCATCATGAACTGCTCATATTTAAATG__AGAGTTTAACTCACTTGGGTTCAGGAATAAGG GAA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:46759251..46759300 32194978 MeRIP-seq:(Medium) rs1206550089 Functional Loss DEL dbSNP153 32..33 33 - - - 59876 RMVar_ID_59876 Human_SNP_ID_464892984 m1A Human chr11 + 46760702 46760702 46760702 TTATGTTCTGTGCACGCTGAGGTTTCTCTTCCACCTGTTTTATTGGTGCAGCAGAGGGTCTCTTT TTATGTTCTGTGCACGCTGAGGTTTCTCTTCCGCCTGTTTTATTGGTGCAGCAGAGGGTCTCTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:46760651..46760725 32194978 MeRIP-seq:(Medium) rs769765445 Functional Loss SNV dbSNP153 33..33 33 - - - 59877 RMVar_ID_59877 Human_SNP_ID_464900060 m1A Human chr11 - 46790536 46790536 46790536 AAAAAGGGGAAACCAGCTGCACCAGGAGGCGCAGGGAATACTGGAACCAAGAACAAGAAAGGACT AAAAAGGGGAAACCAGCTGCACCAGGAGGCGCGGGGAATACTGGAACCAAGAACAAGAAAGGACT T C CKAP5 Ensembl:ENSG00000175216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46790486..46790570 26863196 MeRIP-seq:(Medium) rs768069793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31593,Human_RBP_ID_1457076,Human_RBP_ID_5086832,Human_RBP_ID_6076232,Human_RBP_ID_9275534,Human_RBP_ID_11627971,Human_RBP_ID_19049285,Human_RBP_ID_22642959 Human_Splice_Rec_1234426,Human_Splice_Rec_1234427,Human_Splice_Rec_1234512,Human_Splice_Rec_1234513,Human_Splice_Rec_1234594,Human_Splice_Rec_1234595 RMVar_hsa_circ_82769,RMVar_hsa_circ_265498,RMVar_hsa_circ_149425,RMVar_hsa_circ_4527,RMVar_hsa_circ_4107,RMVar_hsa_circ_69163,RMVar_hsa_circ_15860,RMVar_hsa_circ_102661,RMVar_hsa_circ_149438,RMVar_hsa_circ_376367,RMVar_hsa_circ_21282,RMVar_hsa_circ_9489,RMVar_hsa_circ_10949,RMVar_hsa_circ_149439,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_339610,RMVar_hsa_circ_39382,RMVar_hsa_circ_117759,RMVar_hsa_circ_149446,RMVar_hsa_circ_149447,RMVar_hsa_circ_51065,RMVar_hsa_circ_149449,RMVar_hsa_circ_312680,RMVar_hsa_circ_357143,RMVar_hsa_circ_363341,RMVar_hsa_circ_309573,RMVar_hsa_circ_81884,RMVar_hsa_circ_149451,RMVar_hsa_circ_149452,RMVar_hsa_circ_149450,RMVar_hsa_circ_60445,RMVar_hsa_circ_349067,RMVar_hsa_circ_290955,RMVar_hsa_circ_355600,RMVar_hsa_circ_372343,RMVar_hsa_circ_75739,RMVar_hsa_circ_149457,RMVar_hsa_circ_51687,RMVar_hsa_circ_149454,RMVar_hsa_circ_149455,RMVar_hsa_circ_303570,RMVar_hsa_circ_149453,RMVar_hsa_circ_286354,RMVar_hsa_circ_149456 59878 RMVar_ID_59878 Human_SNP_ID_464900076 m1A Human chr11 - 46790585 46790585 46790585 GTGGTTTAATTTTTATTTTTTAAATTGTTTTTAGGCTGGTGGGCCACCAAAAAAGGGGAAACCAG GTGGTTTAATTTTTATTTTTTAAATTGTTTTTTGGCTGGTGGGCCACCAAAAAAGGGGAAACCAG T A CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:46790576..46790600 26863196 MeRIP-seq:(Medium) rs745369576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9343957,Human_RBP_ID_22641091,Human_RBP_ID_24886837 RMVar_hsa_circ_265498,RMVar_hsa_circ_4527,RMVar_hsa_circ_4107,RMVar_hsa_circ_15860,RMVar_hsa_circ_102661,RMVar_hsa_circ_9489,RMVar_hsa_circ_10949,RMVar_hsa_circ_149439,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_39382,RMVar_hsa_circ_117759,RMVar_hsa_circ_149447,RMVar_hsa_circ_51065,RMVar_hsa_circ_312680,RMVar_hsa_circ_357143,RMVar_hsa_circ_363341,RMVar_hsa_circ_81884,RMVar_hsa_circ_149451,RMVar_hsa_circ_149452,RMVar_hsa_circ_149450,RMVar_hsa_circ_60445,RMVar_hsa_circ_355600,RMVar_hsa_circ_372343,RMVar_hsa_circ_75739,RMVar_hsa_circ_149457,RMVar_hsa_circ_51687,RMVar_hsa_circ_149454,RMVar_hsa_circ_303570,RMVar_hsa_circ_149453 59879 RMVar_ID_59879 Human_SNP_ID_464913266 m1A Human chr11 - 46845897 46845897 46845897 GCAGGGCCGCGCCTGGCGGCAGCGATTTACCAAGACTAGGGCGGGGGCCCCGAGAGCCGGCCCTG GCAGGGCCGCGCCTGGCGGCAGCGATTTACCAGGACTAGGGCGGGGGCCCCGAGAGCCGGCCCTG T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:46845895..46846226 26863196 MeRIP-seq:(Medium) rs886919292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9321375,Human_RBP_ID_26755256,Human_RBP_ID_26775595 59880 RMVar_ID_59880 Human_SNP_ID_464913474 m1A Human chr11 - 46846499 46846491 46846499 GCTGACGACCAAGGATGCCCGGGTCTACACACATTCTTTCGCCTTTCTTTCTGGAGTCGGCAGAC GCTGACGACCAAGGATGCCCGGGTCTACACAC________GCCTTTCTTTCTGGAGTCGGCAGAC CGAAAGAAT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:46846489..46846618 32194978 MeRIP-seq:(Medium) rs1565765720 Functional Loss DEL dbSNP153 33..40 33 - - - 59881 RMVar_ID_59881 Human_SNP_ID_464983690 m1A Human chr11 - 47161678 47161678 47161678 AGGCTGGGTGGGCACACCAAGGGCTGGGTGGGAGCAGGTACAGGGCGCTGTGGGCAGGACCCTTT AGGCTGGGTGGGCACACCAAGGGCTGGGTGGGGGCAGGTACAGGGCGCTGTGGGCAGGACCCTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47161567..47161777 26863196 MeRIP-seq:(Medium) rs775079577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6076891 RMVar_hsa_circ_149481 59882 RMVar_ID_59882 Human_SNP_ID_464990327 m1A Human chr11 - 47182553 47182553 47182553 ATGGCACCCTTTTCCTGTATGCCCAGGCTGGCAACTACAGGCGCACGGTACAGCGGGTGGAGGAC ATGGCACCCTTTTCCTGTATGCCCAGGCTGGCGACTACAGGCGCACGGTACAGCGGGTGGAGGAC T C PACSIN3 Ensembl:ENSG00000165912 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:47182476..47182725 26863196 MeRIP-seq:(Medium) rs751656794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4161531,Human_RBP_ID_5345087 Human_Splice_Rec_1235444,Human_Splice_Rec_1235462,Human_Splice_Rec_1235480,Human_Splice_Rec_1235502,Human_Splice_Rec_1235518,Human_Splice_Rec_1235530,Human_Splice_Rec_1235542,Human_Splice_Rec_1235550,Human_Splice_Rec_1235556,Human_Splice_Rec_1235564 RMVar_hsa_circ_80682,RMVar_hsa_circ_149492,RMVar_hsa_circ_76795,RMVar_hsa_circ_149491 59883 RMVar_ID_59883 Human_SNP_ID_464990395 m1A Human chr11 + 47182739 47182739 47182739 AGCGTCCTCTTCTGGAGCCATGGTGTCCCCGCAGCACGGAATGGTGGCGGATTTGGGGCTGTGGA AGCGTCCTCTTCTGGAGCCATGGTGTCCCCGCGGCACGGAATGGTGGCGGATTTGGGGCTGTGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47182647..47182808 26863196 MeRIP-seq:(Medium) rs1341175153 Functional Loss SNV dbSNP153 33..33 33 - - - 59884 RMVar_ID_59884 Human_SNP_ID_464998385 m1A Human chr11 + 47215167 47215167 47215167 CGATGGCTCCCAAGAAACGCCCAGAAACCCAGAAGACCTCCGAGATTGTATTACGCCCCAGGAAC CGATGGCTCCCAAGAAACGCCCAGAAACCCAGGAGACCTCCGAGATTGTATTACGCCCCAGGAAC A G DDB2 Ensembl:ENSG00000134574 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47215026..47215225 26863196 MeRIP-seq:(Medium) rs762435826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362182,Human_RBP_ID_11631448,Human_RBP_ID_26319750 Human_Splice_Rec_1235566,Human_Splice_Rec_1235567,Human_Splice_Rec_1235572,Human_Splice_Rec_1235573,Human_Splice_Rec_1235581,Human_Splice_Rec_1235599,Human_Splice_Rec_1235621,Human_Splice_Rec_1235625,Human_Splice_Rec_1235653,Human_Splice_Rec_1235667,Human_Splice_Rec_1235677 59885 RMVar_ID_59885 Human_SNP_ID_465003343 m1A Human chr11 - 47235280 47235280 47235280 TGGTCCGTGGTCAGGAGCCGGGCTCCATCGGGACTGAAACAAGCTGGCAAAGTGAAAAGCCCCTG TGGTCCGTGGTCAGGAGCCGGGCTCCATCGGGGCTGAAACAAGCTGGCAAAGTGAAAAGCCCCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:47235264..47235365 32194978 MeRIP-seq:(Medium) rs1386384686 Functional Loss SNV dbSNP153 33..33 33 - - - 59886 RMVar_ID_59886 Human_SNP_ID_465007042 m1A Human chr11 - 47248972 47248972 47248972 GTTACCTTCTTATGCTCCTCCGCCACAGCCAGACCACGACCCTCCTGCACGCAATCCCACCGAGA GTTACCTTCTTATGCTCCTCCGCCACAGCCAGCCCACGACCCTCCTGCACGCAATCCCACCGAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47248924..47249060 26863196 MeRIP-seq:(Medium) rs1238791297 Functional Loss SNV dbSNP153 33..33 33 - - - 59887 RMVar_ID_59887 Human_SNP_ID_465010014 m1A Human chr11 - 47259768 47259768 47259768 ACCGCAGAGTCTGAGCTCCAAAAGAGAGGCACAAGGGGGTCTCAGGCCCCATCCCGGCTCCACGG ACCGCAGAGTCTGAGCTCCAAAAGAGAGGCACGAGGGGGTCTCAGGCCCCATCCCGGCTCCACGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47259765..47259836 26863196 MeRIP-seq:(Medium) rs1297280081 Functional Loss SNV dbSNP153 33..33 33 - - - 59888 RMVar_ID_59888 Human_SNP_ID_465010045 m1A Human chr11 + 47259835 47259835 47259835 AGCTGTGGAAGCCAGGCGCACAGGATGCAAGCAGCCAGGCCCAGGGAGGCAGCAGCTGCATCCTC AGCTGTGGAAGCCAGGCGCACAGGATGCAAGCTGCCAGGCCCAGGGAGGCAGCAGCTGCATCCTC A T NR1H3 Ensembl:ENSG00000025434 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:47259765..47259853;chr11:47259746..47259836 26863196 MeRIP-seq:(Medium) rs921841556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751930,Human_RBP_ID_867400,Human_RBP_ID_9363553,Human_RBP_ID_18971912,Human_RBP_ID_19049324 Human_Splice_Rec_1235944,Human_Splice_Rec_1235950,Human_Splice_Rec_1235962,Human_Splice_Rec_1235980,Human_Splice_Rec_1235996,Human_Splice_Rec_1236012,Human_Splice_Rec_1236026,Human_Splice_Rec_1236040,Human_Splice_Rec_1236058,Human_Splice_Rec_1236066,Human_Splice_Rec_1236082,Human_Splice_Rec_1236100,Human_Splice_Rec_1236110,Human_Splice_Rec_1236112,Human_Splice_Rec_1236122,Human_Splice_Rec_1236136,Human_Splice_Rec_1236140,Human_Splice_Rec_1236148,Human_Splice_Rec_1236152,Human_Splice_Rec_1236158,Human_Splice_Rec_1236164,Human_Splice_Rec_1236182,Human_Splice_Rec_1236190,Human_Splice_Rec_1236208,Human_Splice_Rec_1236222,Human_Splice_Rec_1236228,Human_Splice_Rec_1236232,Human_Splice_Rec_1236234 RMVar_hsa_circ_63435,RMVar_hsa_circ_362738 59889 RMVar_ID_59889 Human_SNP_ID_465014313 m1A Human chr11 + 47274897 47274897 47274897 CCCATGCCACCTGTGCCTCAGAAGAGGGTGGCACTGAGAGCTCAGAGAGTGGCTCATCCCTGCAG CCCATGCCACCTGTGCCTCAGAAGAGGGTGGCGCTGAGAGCTCAGAGAGTGGCTCATCCCTGCAG A G MADD Ensembl:ENSG00000110514 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:47274851..47275063 26863196 MeRIP-seq:(Medium) rs759062609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8769589 RMVar_hsa_circ_13669,RMVar_hsa_circ_85527,RMVar_hsa_circ_53340,RMVar_hsa_circ_149510,RMVar_hsa_circ_359569,RMVar_hsa_circ_19602,RMVar_hsa_circ_149511,RMVar_hsa_circ_111860 59890 RMVar_ID_59890 Human_SNP_ID_465017125 m1A Human chr11 - 47284402 47284402 47284402 GCTCGTCAATCTCCACCTCGCTGGCATCCCCCAGTGCTGCATGTGTCAGAGGGTCCACATCTGCC GCTCGTCAATCTCCACCTCGCTGGCATCCCCCGGTGCTGCATGTGTCAGAGGGTCCACATCTGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:47284288..47284406 32194978 MeRIP-seq:(Medium) rs1375636782 Functional Loss SNV dbSNP153 33..33 33 - - - 59891 RMVar_ID_59891 Human_SNP_ID_465054401 m1A Human chr11 + 47413523 47413522 47413524 TGGTCCGGAGCATCAAAGTGAGTGGCCTGCTCAGGGCCCCTGCAGCCGTACTGCCCTGAGTGGCC TGGTCCGGAGCATCAAAGTGAGTGGCCTGCTC__GGCCCCTGCAGCCGTACTGCCCTGAGTGGCC CAG C SLC39A13 Ensembl:ENSG00000165915 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47413521..47413590 26863196 MeRIP-seq:(Medium) rs764548331 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_149527,RMVar_hsa_circ_340541 59892 RMVar_ID_59892 Human_SNP_ID_465054403 m1A Human chr11 + 47413523 47413523 47413523 TGGTCCGGAGCATCAAAGTGAGTGGCCTGCTCAGGGCCCCTGCAGCCGTACTGCCCTGAGTGGCC TGGTCCGGAGCATCAAAGTGAGTGGCCTGCTCGGGGCCCCTGCAGCCGTACTGCCCTGAGTGGCC A G SLC39A13 Ensembl:ENSG00000165915 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47413521..47413590 26863196 MeRIP-seq:(Medium) rs772265206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149527,RMVar_hsa_circ_340541 59893 RMVar_ID_59893 Human_SNP_ID_465054541 m1A Human chr11 + 47413916 47413916 47413916 TACTCCTTGTTGGGTGCCTCTGTCAAGCTGCTAGGCGTGGCCCCTGCCTGCTCCTAGATGCTTCT TACTCCTTGTTGGGTGCCTCTGTCAAGCTGCTGGGCGTGGCCCCTGCCTGCTCCTAGATGCTTCT A G SLC39A13 Ensembl:ENSG00000165915 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:47413913..47414015 26863196 MeRIP-seq:(Medium) rs1283421935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18933463,Human_RBP_ID_21965269 59894 RMVar_ID_59894 Human_SNP_ID_465057644 m1A Human chr11 - 47424099 47424099 47424099 ACTCGCGGGTGAAGGCCATGGAGGTAGACGAGAGGCCCACGGAGCAATACAGTGACATTGGGGGT ACTCGCGGGTGAAGGCCATGGAGGTAGACGAGGGGCCCACGGAGCAATACAGTGACATTGGGGGT T C PSMC3 Ensembl:ENSG00000165916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47424035..47424209 26863196 MeRIP-seq:(Medium) rs1270594616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1457161,Human_RBP_ID_11632756,Human_RBP_ID_17796624,Human_RBP_ID_22435220,Human_RBP_ID_26319757 Human_Splice_Rec_1237356,Human_Splice_Rec_1237357,Human_Splice_Rec_1237378,Human_Splice_Rec_1237379,Human_Splice_Rec_1237400,Human_Splice_Rec_1237401,Human_Splice_Rec_1237420,Human_Splice_Rec_1237421,Human_Splice_Rec_1237442,Human_Splice_Rec_1237460,Human_Splice_Rec_1237461,Human_Splice_Rec_1237474,Human_Splice_Rec_1237475,Human_Splice_Rec_1237486,Human_Splice_Rec_1237487,Human_Splice_Rec_1237500,Human_Splice_Rec_1237501,Human_Splice_Rec_1237512 RMVar_hsa_circ_107277,RMVar_hsa_circ_124811,RMVar_hsa_circ_114541,RMVar_hsa_circ_7626,RMVar_hsa_circ_102948,RMVar_hsa_circ_149538,RMVar_hsa_circ_149540,RMVar_hsa_circ_83569,RMVar_hsa_circ_149539,RMVar_hsa_circ_149536,RMVar_hsa_circ_149537,RMVar_hsa_circ_102589,RMVar_hsa_circ_149541,RMVar_hsa_circ_371684,RMVar_hsa_circ_85347,RMVar_hsa_circ_21308,RMVar_hsa_circ_55740,RMVar_hsa_circ_149545,RMVar_hsa_circ_149546,RMVar_hsa_circ_116633,RMVar_hsa_circ_149547 59895 RMVar_ID_59895 Human_SNP_ID_465057729 m1A Human chr11 - 47424438 47424438 47424438 GGGTTGGTGGATGCTGAAAAGCTAAAGCCAGGAGACCTGGTGGTGAGTGGGGCCTGAGCCCAGGC GGGTTGGTGGATGCTGAAAAGCTAAAGCCAGGCGACCTGGTGGTGAGTGGGGCCTGAGCCCAGGC T G PSMC3 Ensembl:ENSG00000165916 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:47424426..47424500 32194978 MeRIP-seq:(Medium) rs759608633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4190743,Human_RBP_ID_9275550,Human_RBP_ID_19051495,Human_RBP_ID_22435222 Human_Splice_Rec_1237354,Human_Splice_Rec_1237355,Human_Splice_Rec_1237376,Human_Splice_Rec_1237377,Human_Splice_Rec_1237398,Human_Splice_Rec_1237399,Human_Splice_Rec_1237418,Human_Splice_Rec_1237419,Human_Splice_Rec_1237440,Human_Splice_Rec_1237441,Human_Splice_Rec_1237458,Human_Splice_Rec_1237459,Human_Splice_Rec_1237472,Human_Splice_Rec_1237473,Human_Splice_Rec_1237498,Human_Splice_Rec_1237499,Human_Splice_Rec_1237510,Human_Splice_Rec_1237511,Human_Splice_Rec_1237520 RMVar_hsa_circ_107277,RMVar_hsa_circ_114541,RMVar_hsa_circ_102948,RMVar_hsa_circ_149538,RMVar_hsa_circ_149540,RMVar_hsa_circ_83569,RMVar_hsa_circ_149539,RMVar_hsa_circ_149537,RMVar_hsa_circ_102589,RMVar_hsa_circ_149541,RMVar_hsa_circ_371684,RMVar_hsa_circ_85347,RMVar_hsa_circ_21308,RMVar_hsa_circ_55740,RMVar_hsa_circ_149545,RMVar_hsa_circ_149546,RMVar_hsa_circ_116633,RMVar_hsa_circ_94331,RMVar_hsa_circ_149547,RMVar_hsa_circ_149548 59896 RMVar_ID_59896 Human_SNP_ID_465057936 m1A Human chr11 - 47425205 47425205 47425205 AGTGAAGTGTTGAGAGTCACCCATGAGCTCCAAGCCATGAAGGACAAGATAAAAGAGAACAGTGA AGTGAAGTGTTGAGAGTCACCCATGAGCTCCAGGCCATGAAGGACAAGATAAAAGAGAACAGTGA T C PSMC3 Ensembl:ENSG00000165916 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:47425101..47425466;chr11:47425101..47425299 26863196 MeRIP-seq:(Medium) rs560520604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1779596,Human_RBP_ID_4161852,Human_RBP_ID_9362200,Human_RBP_ID_17648672,Human_RBP_ID_18410480,Human_RBP_ID_18525838,Human_RBP_ID_26318269 Human_Splice_Rec_1237350,Human_Splice_Rec_1237351,Human_Splice_Rec_1237372,Human_Splice_Rec_1237373,Human_Splice_Rec_1237394,Human_Splice_Rec_1237395,Human_Splice_Rec_1237436,Human_Splice_Rec_1237437,Human_Splice_Rec_1237454,Human_Splice_Rec_1237455,Human_Splice_Rec_1237468,Human_Splice_Rec_1237469,Human_Splice_Rec_1237482,Human_Splice_Rec_1237483,Human_Splice_Rec_1237494,Human_Splice_Rec_1237495,Human_Splice_Rec_1237506,Human_Splice_Rec_1237507,Human_Splice_Rec_1237516,Human_Splice_Rec_1237517,Human_Splice_Rec_1237524,Human_Splice_Rec_1237525 Human_miRNA_ID_2043195,Human_miRNA_ID_2045346,Human_miRNA_ID_2195472,Human_miRNA_ID_2254925,Human_miRNA_ID_2615442 RMVar_hsa_circ_107277,RMVar_hsa_circ_149540,RMVar_hsa_circ_83569,RMVar_hsa_circ_149539,RMVar_hsa_circ_371684,RMVar_hsa_circ_85347,RMVar_hsa_circ_21308,RMVar_hsa_circ_55740,RMVar_hsa_circ_149545,RMVar_hsa_circ_149546,RMVar_hsa_circ_345488,RMVar_hsa_circ_32022 59897 RMVar_ID_59897 Human_SNP_ID_465058126 m1A Human chr11 + 47425945 47425945 47425945 GTGGACATCTTGAGCACCTCCTCCCCAATTCCATCTTGCTGTAAAAAATTATTTGTTTATTTATA GTGGACATCTTGAGCACCTCCTCCCCAATTCCGTCTTGCTGTAAAAAATTATTTGTTTATTTATA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:47425827..47425998;chr11:47425841..47426455;chr11:47425829..47426439;chr11:47425831..47426004 26863196 MeRIP-seq:(Medium) rs1220865773 Functional Loss SNV dbSNP153 33..33 33 - - - 59898 RMVar_ID_59898 Human_SNP_ID_465058274 m1A Human chr11 - 47426332 47426332 47426332 GTCAAGAGAAGGCTTTAAGAAAGACGGTATTAATCTCCCGTTGCGGCTCCCGCCTGGTCCCATCT GTCAAGAGAAGGCTTTAAGAAAGACGGTATTAGTCTCCCGTTGCGGCTCCCGCCTGGTCCCATCT T C PSMC3 Ensembl:ENSG00000165916 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:47426281..47426434 26863196 MeRIP-seq:(Medium) rs756826237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4161864 Human_miRNA_ID_3011565 RMVar_hsa_circ_149540,RMVar_hsa_circ_83569,RMVar_hsa_circ_85347,RMVar_hsa_circ_149546 59899 RMVar_ID_59899 Human_SNP_ID_465069412 m1A Human chr11 + 47468002 47468002 47468002 TGATATATACGAAGGTGTGAAGAAACAGCAGGAAACATGCAAAACTTTTTTCTGGGCATAATCTT TGATATATACGAAGGTGTGAAGAAACAGCAGGTAACATGCAAAACTTTTTTCTGGGCATAATCTT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:47467951..47468149 26863196 MeRIP-seq:(Medium) rs1256622639 Functional Loss SNV dbSNP153 33..33 33 - - - 59900 RMVar_ID_59900 Human_SNP_ID_465069430 m1A Human chr11 + 47468077 47468077 47468077 GAAAAAATTCAAAACAAAAACACAAAAACAATACAAAAACAAAAACAACAACAAAAAAATCAAAG GAAAAAATTCAAAACAAAAACACAAAAACAATGCAAAAACAAAAACAACAACAAAAAAATCAAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:47468026..47468200 32194978 MeRIP-seq:(Medium) rs988770978 Functional Loss SNV dbSNP153 33..33 33 - - - 59901 RMVar_ID_59901 Human_SNP_ID_465069945 m1A Human chr11 - 47470287 47470287 47470287 ATAAAAAAGAAAAAAGAAAACAAAAAAAAAAAAGAAAAAAATGCTAGGTTGGGGAGGCGCTGTTC ATAAAAAAGAAAAAAGAAAACAAAAAAAAAAAGGAAAAAAATGCTAGGTTGGGGAGGCGCTGTTC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs199952011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119120,RMVar_hsa_circ_125906,RMVar_hsa_circ_122378,RMVar_hsa_circ_149549,RMVar_hsa_circ_149550,RMVar_hsa_circ_149551 59902 RMVar_ID_59902 Human_SNP_ID_465074819 m1A Human chr11 - 47489021 47489021 47489021 TAATAGAAGTTTCATTTTATCTCACACAGCTCAAAGAAAATGAACGGCACCCTGGACCACCCAGA TAATAGAAGTTTCATTTTATCTCACACAGCTCGAAGAAAATGAACGGCACCCTGGACCACCCAGA T C CELF1 Ensembl:ENSG00000149187 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47489001..47489025 26863196 MeRIP-seq:(Medium) rs1267094641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870000,Human_RBP_ID_3940419,Human_RBP_ID_4190806,Human_RBP_ID_9004107,Human_RBP_ID_9362211,Human_RBP_ID_11634004,Human_RBP_ID_24916681,Human_RBP_ID_27804412 Human_Splice_Rec_1237576,Human_Splice_Rec_1237650,Human_Splice_Rec_1237712,Human_Splice_Rec_1237742,Human_Splice_Rec_1237792,Human_Splice_Rec_1237802,Human_Splice_Rec_1237808,Human_Splice_Rec_1237814,Human_Splice_Rec_1237818,Human_Splice_Rec_1237822,Human_Splice_Rec_1237832,Human_Splice_Rec_1237838 RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_11194,RMVar_hsa_circ_348304,RMVar_hsa_circ_341549,RMVar_hsa_circ_149561,RMVar_hsa_circ_72610,RMVar_hsa_circ_370104,RMVar_hsa_circ_342676,RMVar_hsa_circ_296993,RMVar_hsa_circ_149563,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_272133,RMVar_hsa_circ_149566,RMVar_hsa_circ_149575,RMVar_hsa_circ_270573,RMVar_hsa_circ_116927,RMVar_hsa_circ_149568,RMVar_hsa_circ_272507,RMVar_hsa_circ_52645,RMVar_hsa_circ_149573,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_290310,RMVar_hsa_circ_149576 59903 RMVar_ID_59903 Human_SNP_ID_465092467 m1A Human chr11 - 47553064 47553064 47553064 ACGCGGAGGCTCCCCCGGGATTCGGCCTCAGCAGCGAGGCGGCGGCGGCGGCTGCGGAGGCGCAG ACGCGGAGGCTCCCCCGGGATTCGGCCTCAGCTGCGAGGCGGCGGCGGCGGCTGCGGAGGCGCAG T A CELF1 Ensembl:ENSG00000149187 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47552976..47553150 26863196 MeRIP-seq:(Medium) rs995030778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227720,Human_RBP_ID_3940420,Human_RBP_ID_4162140,Human_RBP_ID_18416549,Human_RBP_ID_27804413 Human_Splice_Rec_1237575,Human_Splice_Rec_1237707 59904 RMVar_ID_59904 Human_SNP_ID_465092477 m1A Human chr11 - 47553077 47553077 47553077 CAGCGGCGGCGGGACGCGGAGGCTCCCCCGGGATTCGGCCTCAGCAGCGAGGCGGCGGCGGCGGC CAGCGGCGGCGGGACGCGGAGGCTCCCCCGGGCTTCGGCCTCAGCAGCGAGGCGGCGGCGGCGGC T G CELF1 Ensembl:ENSG00000149187 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:47552973..47553127;chr11:47552997..47553110;chr11:47552961..47553125;chr11:47552976..47553150;chr11:47552965..47553125 26863196 MeRIP-seq:(Medium) rs1449052470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227720,Human_RBP_ID_3940420,Human_RBP_ID_4162142,Human_RBP_ID_18416550,Human_RBP_ID_22034408,Human_RBP_ID_27804413 Human_Splice_Rec_1237575,Human_Splice_Rec_1237707 59905 RMVar_ID_59905 Human_SNP_ID_465095915 m1A Human chr11 - 47565424 47565424 47565424 CTGGAGGAGGGCCCGGCGGCCTCGGAGGAGGGACCGAGGTTTCCTGGGCGGGAAACTGGGACCCC CTGGAGGAGGGCCCGGCGGCCTCGGAGGAGGGCCCGAGGTTTCCTGGGCGGGAAACTGGGACCCC T G CELF1 Ensembl:ENSG00000149187 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:47565375..47565495 26863196 MeRIP-seq:(Medium) rs947873190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17066991 59906 RMVar_ID_59906 Human_SNP_ID_465096094 m1A Human chr11 - 47565879 47565879 47565879 TACCAGCTGCCGAGGCAAAGAGGTGGCTCAGCAAAGACGGTGGAGACCCCAGCGGCCCGACAGGG TACCAGCTGCCGAGGCAAAGAGGTGGCTCAGCGAAGACGGTGGAGACCCCAGCGGCCCGACAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:47565876..47565900 26863196 MeRIP-seq:(Medium) rs530786983 Functional Loss SNV dbSNP153 33..33 33 - - - 59907 RMVar_ID_59907 Human_SNP_ID_465096114 m1A Human chr11 + 47565919 47565919 47565919 CACCTCTTTGCCTCGGCAGCTGGTACAGGACGAGAACGTGCGCGGGGTGATCACCATGAACGAGG CACCTCTTTGCCTCGGCAGCTGGTACAGGACGGGAACGTGCGCGGGGTGATCACCATGAACGAGG A G PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47565335..47566005 26863196 MeRIP-seq:(Medium) rs770334751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397198,Human_RBP_ID_867417,Human_RBP_ID_1162163,Human_RBP_ID_1457297,Human_RBP_ID_4184817,Human_RBP_ID_11636340,Human_RBP_ID_22569091,Human_RBP_ID_23507698 Human_Splice_Rec_1237842,Human_Splice_Rec_1237843,Human_Splice_Rec_1237913,Human_Splice_Rec_1237915,Human_Splice_Rec_1237920,Human_Splice_Rec_1237921,Human_Splice_Rec_1237924,Human_Splice_Rec_1237925,Human_Splice_Rec_1237929 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582 59908 RMVar_ID_59908 Human_SNP_ID_465099416 m1A Human chr11 + 47577968 47577968 47577968 TGAAAGTGTAGTTCACAAAGTAGTTCTCATCCATGGATGCTCCAGGCTCCTCTGGTGATTCCATG TGAAAGTGTAGTTCACAAAGTAGTTCTCATCCGTGGATGCTCCAGGCTCCTCTGGTGATTCCATG A G KF459542.1,NDUFS3 Ensembl:ENSG00000231880,Ensembl:ENSG00000213619 lincRNA,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47577917..47578047 26863196 MeRIP-seq:(Medium) rs1176296527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246022,Human_RBP_ID_8247179 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584 59909 RMVar_ID_59909 Human_SNP_ID_465099844 m1A Human chr11 - 47579122 47579122 47579122 GGTCAGCGCCGAGGCCCCCAAGATCCCGCGCCACCACAGCCTGGCTACCGCCGCCGCCGCCATGT GGTCAGCGCCGAGGCCCCCAAGATCCCGCGCCGCCACAGCCTGGCTACCGCCGCCGCCGCCATGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:47579076..47579286 26863196 MeRIP-seq:(Medium) rs1297486508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149587 59910 RMVar_ID_59910 Human_SNP_ID_465099852 m1A Human chr11 - 47579134 47579134 47579134 GTGCTCACCCCTGGTCAGCGCCGAGGCCCCCAAGATCCCGCGCCACCACAGCCTGGCTACCGCCG GTGCTCACCCCTGGTCAGCGCCGAGGCCCCCAGGATCCCGCGCCACCACAGCCTGGCTACCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47579051..47579386 26863196 MeRIP-seq:(Medium) rs780719617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149587 59911 RMVar_ID_59911 Human_SNP_ID_465099948 m1A Human chr11 + 47579311 47579311 47579311 ACCCTCCGTTCTGTTGCTGCCGGTGAGGCGGGAGAGCGCCGGGGCCGACACGCGCCGTGAGTATG ACCCTCCGTTCTGTTGCTGCCGGTGAGGCGGGGGAGCGCCGGGGCCGACACGCGCCGTGAGTATG A G NDUFS3 Ensembl:ENSG00000213619 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:47579076..47579350 26863410 MeRIP-seq:(Medium) rs1469806098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750834,Human_RBP_ID_807999,Human_RBP_ID_4184821,Human_RBP_ID_5110405,Human_RBP_ID_9321384,Human_RBP_ID_19049357,Human_RBP_ID_22432888,Human_RBP_ID_26775763,Human_RBP_ID_27836312 Human_Splice_Rec_1237854,Human_Splice_Rec_1237856,Human_Splice_Rec_1237857,Human_Splice_Rec_1237868,Human_Splice_Rec_1237869,Human_Splice_Rec_1237872,Human_Splice_Rec_1237873,Human_Splice_Rec_1237878,Human_Splice_Rec_1237879,Human_Splice_Rec_1237889,Human_Splice_Rec_1237891,Human_Splice_Rec_1237899 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_149588,RMVar_hsa_circ_88849 59912 RMVar_ID_59912 Human_SNP_ID_465100363 m1A Human chr11 - 47580482 47580482 47580482 AAGGCATATTTAAAAAAGAAATGGAGAAGGCAAAAGCCAGCCCTGCATGCAGTCTCTTAGGCTTG AAGGCATATTTAAAAAAGAAATGGAGAAGGCAGAAGCCAGCCCTGCATGCAGTCTCTTAGGCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47580479..47580614 26863196 MeRIP-seq:(Medium) rs1313391930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149587 59913 RMVar_ID_59913 Human_SNP_ID_465100511 m1A Human chr11 - 47580866 47580851 47580867 AAGTCAGCACTGGGATGACGCCATCAGGATGGATACAGACCTCTAACTCATTGAAGCAGGACACC AAGTCAGCACTGGGATGACGCCATCAGGATG________________TCATTGAAGCAGGACACC AGTTAGAGGTCTGTATC A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:47580857..47581006 32194978 MeRIP-seq:(Medium) rs765444983 Functional Loss DEL dbSNP153 32..47 33 - - - RMVar_hsa_circ_149587 59914 RMVar_ID_59914 Human_SNP_ID_465100852 m1A Human chr11 + 47582152 47582152 47582152 CTCACGGATCCGTGTGAAGACCTACACAGATGAGCTGACGCCCATTGAGTCTGCTGTCTCTGTGT CTCACGGATCCGTGTGAAGACCTACACAGATGCGCTGACGCCCATTGAGTCTGCTGTCTCTGTGT A C NDUFS3 Ensembl:ENSG00000213619 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47582101..47582242 26863196 MeRIP-seq:(Medium) rs770110842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397246,Human_RBP_ID_987254,Human_RBP_ID_1457313,Human_RBP_ID_11636584,Human_RBP_ID_17234050 Human_Splice_Rec_1237848,Human_Splice_Rec_1237849,Human_Splice_Rec_1237884,Human_Splice_Rec_1237885,Human_Splice_Rec_1237896,Human_Splice_Rec_1237897,Human_Splice_Rec_1237903,Human_Splice_Rec_1237907 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_84774,RMVar_hsa_circ_149588,RMVar_hsa_circ_88849,RMVar_hsa_circ_149591,RMVar_hsa_circ_149590,RMVar_hsa_circ_270308 59915 RMVar_ID_59915 Human_SNP_ID_465100853 m1A Human chr11 + 47582152 47582152 47582152 CTCACGGATCCGTGTGAAGACCTACACAGATGAGCTGACGCCCATTGAGTCTGCTGTCTCTGTGT CTCACGGATCCGTGTGAAGACCTACACAGATGGGCTGACGCCCATTGAGTCTGCTGTCTCTGTGT A G NDUFS3 Ensembl:ENSG00000213619 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47582101..47582242 26863196 MeRIP-seq:(Medium) rs770110842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397246,Human_RBP_ID_987254,Human_RBP_ID_1457313,Human_RBP_ID_11636584,Human_RBP_ID_17234050 Human_Splice_Rec_1237848,Human_Splice_Rec_1237849,Human_Splice_Rec_1237884,Human_Splice_Rec_1237885,Human_Splice_Rec_1237896,Human_Splice_Rec_1237897,Human_Splice_Rec_1237903,Human_Splice_Rec_1237907 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_84774,RMVar_hsa_circ_149588,RMVar_hsa_circ_88849,RMVar_hsa_circ_149591,RMVar_hsa_circ_149590,RMVar_hsa_circ_270308 59916 RMVar_ID_59916 Human_SNP_ID_465101462 m1A Human chr11 + 47584370 47584370 47584370 CGGGTGGTGGCAGAGCCGGTGGAGTTGGCCCAAGAGTTCCGCAAATTTGACCTGAACAGCCCCTG CGGGTGGTGGCAGAGCCGGTGGAGTTGGCCCAGGAGTTCCGCAAATTTGACCTGAACAGCCCCTG A G NDUFS3 Ensembl:ENSG00000213619 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47584286..47584504 26863196 MeRIP-seq:(Medium) rs747604324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397251,Human_RBP_ID_750837,Human_RBP_ID_5110406,Human_RBP_ID_5138867,Human_RBP_ID_9004138,Human_RBP_ID_17649063,Human_RBP_ID_17804541,Human_RBP_ID_22433522,Human_RBP_ID_22753446,Human_RBP_ID_23206914,Human_RBP_ID_23507761,Human_RBP_ID_26319763 Human_Splice_Rec_1237852,Human_Splice_Rec_1237888,Human_Splice_Rec_1237906,Human_Splice_Rec_1237910,Human_Splice_Rec_1237912 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_84774,RMVar_hsa_circ_149590 59917 RMVar_ID_59917 Human_SNP_ID_465110762 m1A Human chr11 + 47618860 47618860 47618860 CATCTTCAAATTAACATTTTCAGGTCACAACAATAAGTCTTCCCAAAGGGGACCTTCCGGAAAAA CATCTTCAAATTAACATTTTCAGGTCACAACAGTAAGTCTTCCCAAAGGGGACCTTCCGGAAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:47618751..47618900 32194978 MeRIP-seq:(Medium) rs200224785 Functional Loss SNV dbSNP153 33..33 33 - - - 59918 RMVar_ID_59918 Human_SNP_ID_465116065 m1A Human chr11 + 47639031 47639031 47639031 TGCCGCCCAAAAATATTTCGTCCTATTGTTGGAGGAAGAGGCTCATATCCCACCTTTAAAAACAA TGCCGCCCAAAAATATTTCGTCCTATTGTTGGGGGAAGAGGCTCATATCCCACCTTTAAAAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47638980..47642550 26863196 MeRIP-seq:(Medium) rs1355103595 Functional Loss SNV dbSNP153 33..33 33 - - - 59919 RMVar_ID_59919 Human_SNP_ID_465143467 m1A Human chr11 - 47746234 47746234 47746234 AATTTGTAAAGAGGAGCCAGTTTCAGAAGTAAAAGAAACAAGTACAACAGTAGAAGAAGCAACAA AATTTGTAAAGAGGAGCCAGTTTCAGAAGTAAGAGAAACAAGTACAACAGTAGAAGAAGCAACAA T C FNBP4 Ensembl:ENSG00000109920 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47746105..47746350 26863196 MeRIP-seq:(Medium) rs767713162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29742,Human_RBP_ID_867431,Human_RBP_ID_1461974,Human_RBP_ID_2271209,Human_RBP_ID_3940432,Human_RBP_ID_5520689,Human_RBP_ID_18410590,Human_RBP_ID_22035888,Human_RBP_ID_24542330,Human_RBP_ID_26318292,Human_RBP_ID_27803412 Human_miRNA_ID_2477609 RMVar_hsa_circ_5588,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_360503,RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_44057,RMVar_hsa_circ_79080,RMVar_hsa_circ_149626,RMVar_hsa_circ_341159,RMVar_hsa_circ_280985,RMVar_hsa_circ_275399,RMVar_hsa_circ_347418,RMVar_hsa_circ_149628,RMVar_hsa_circ_149630,RMVar_hsa_circ_287,RMVar_hsa_circ_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_71587,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354019,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,RMVar_hsa_circ_350437,RMVar_hsa_circ_359423,RMVar_hsa_circ_329619,RMVar_hsa_circ_68679,RMVar_hsa_circ_149643,RMVar_hsa_circ_149640,RMVar_hsa_circ_149641,RMVar_hsa_circ_149642,RMVar_hsa_circ_58118,RMVar_hsa_circ_294542 59920 RMVar_ID_59920 Human_SNP_ID_465149808 m1A Human chr11 + 47767226 47767226 47767226 TCCGGGTCCCGGCCCGGCGTGCTGCCCCGAGGACCCGGCGGAGAGAGTTGCAGGATGGGCCTACG TCCGGGTCCCGGCCCGGCGTGCTGCCCCGAGGGCCCGGCGGAGAGAGTTGCAGGATGGGCCTACG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:47767176..47767250 26863196 MeRIP-seq:(Medium) rs1375906594 Functional Loss SNV dbSNP153 33..33 33 - - - 59921 RMVar_ID_59921 Human_SNP_ID_465149820 m1A Human chr11 - 47767241 47767241 47767241 CGGGCGGTACCCGGCCGTAGGCCCATCCTGCAACTCTCTCCGCCGGGTCCTCGGGGCAGCACGCC CGGGCGGTACCCGGCCGTAGGCCCATCCTGCAGCTCTCTCCGCCGGGTCCTCGGGGCAGCACGCC T C FNBP4 Ensembl:ENSG00000109920 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:47767191..47767289 26863196 MeRIP-seq:(Medium) rs1191697115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108559,Human_RBP_ID_4184828,Human_RBP_ID_8769711 RMVar_hsa_circ_90929,RMVar_hsa_circ_149650 59922 RMVar_ID_59922 Human_SNP_ID_465170390 m1A Human chr11 - 47844067 47844067 47844067 GGATGGGGAGTATACAGAAAGAAAAGAGTCACAGGTGAGCCCTAGATTTTTGGCTTGAGCAATTG GGATGGGGAGTATACAGAAAGAAAAGAGTCACTGGTGAGCCCTAGATTTTTGGCTTGAGCAATTG T A NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:47844064..47844624 26863196 MeRIP-seq:(Medium) rs1227608832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_43917,RMVar_hsa_circ_149711,RMVar_hsa_circ_86024 59923 RMVar_ID_59923 Human_SNP_ID_465203612 m1A Human chr11 + 47980805 47980805 47980805 GCGGAGCGGGGACGAGGCGGACCGGCTGGCGGAGGAGGAGGCGAAGGAGACGGCAGGAGGCGGCG GCGGAGCGGGGACGAGGCGGACCGGCTGGCGGGGGAGGAGGCGAAGGAGACGGCAGGAGGCGGCG A G PTPRJ Ensembl:ENSG00000149177 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:47980479..47980991;chr11:47980489..47981007;chr11:47980532..47980838 26863196 MeRIP-seq:(Medium) rs1025183572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3384110,Human_RBP_ID_9275556,Human_RBP_ID_9414491 59924 RMVar_ID_59924 Human_SNP_ID_465210147 m1A Human chr11 + 48007758 48007758 48007758 GTCTTCCCTCCAGGCAGCAGCAAGCTGGTAGGAGCTGTACTTGTGAGTTGACATCATGATGTACA GTCTTCCCTCCAGGCAGCAGCAAGCTGGTAGGTGCTGTACTTGTGAGTTGACATCATGATGTACA A T PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:48007754..48007890 26863196 MeRIP-seq:(Medium) rs904569823 Functional Loss SNV dbSNP153 33..33 33 - - - 59925 RMVar_ID_59925 Human_SNP_ID_465226888 m1A Human chr11 + 48078425 48078425 48078425 TGGGTTTCGGCAGTTCAGGTTGTTAGGAGACAAGGGTGGAAAGGTGTCCTGGAGCCCTACAGAGA TGGGTTTCGGCAGTTCAGGTTGTTAGGAGACACGGGTGGAAAGGTGTCCTGGAGCCCTACAGAGA A C PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:48078423..48078631 26863196 MeRIP-seq:(Medium) rs1365059324 Functional Loss SNV dbSNP153 33..33 33 - - - 59926 RMVar_ID_59926 Human_SNP_ID_465226889 m1A Human chr11 + 48078425 48078425 48078425 TGGGTTTCGGCAGTTCAGGTTGTTAGGAGACAAGGGTGGAAAGGTGTCCTGGAGCCCTACAGAGA TGGGTTTCGGCAGTTCAGGTTGTTAGGAGACAGGGGTGGAAAGGTGTCCTGGAGCCCTACAGAGA A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:48078423..48078631 26863196 MeRIP-seq:(Medium) rs1365059324 Functional Loss SNV dbSNP153 33..33 33 - - - 59927 RMVar_ID_59927 Human_SNP_ID_123745397 m1A Human chr3 - 15003927 15003927 15003927 AGAGTCGGTGGAGATTATCTGGATGCGTGGGGAGGGGCTGGTCATCCCTGGAGATTCCGGCCGAG AGAGTCGGTGGAGATTATCTGGATGCGTGGGGTGGGGCTGGTCATCCCTGGAGATTCCGGCCGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:15003828..15003949;chr3:15003815..15003979 26863196 MeRIP-seq:(Medium) rs762363329 Functional Loss SNV dbSNP153 33..33 33 - - - 59928 RMVar_ID_59928 Human_SNP_ID_123758136 m1A Human chr3 - 15052498 15052498 15052498 GGGCAGGTGCCCTGCCCCAGCCTGGTGCCATTACCCAAGGAGATGAGGGGGAAGTACAAAGCCGC GGGCAGGTGCCCTGCCCCAGCCTGGTGCCATTGCCCAAGGAGATGAGGGGGAAGTACAAAGCCGC T C MRPS25 Ensembl:ENSG00000131368 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:15052376..15052525 32194978 MeRIP-seq:(Medium) rs1245027742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592779,Human_RBP_ID_934856,Human_RBP_ID_14673779,Human_RBP_ID_17996745,Human_RBP_ID_18799614,Human_RBP_ID_19011567,Human_RBP_ID_19115120,Human_RBP_ID_22091491,Human_RBP_ID_22455340,Human_RBP_ID_22822488,Human_RBP_ID_23026469,Human_RBP_ID_23119959,Human_RBP_ID_26346240,Human_RBP_ID_27047560,Human_RBP_ID_27821959 59929 RMVar_ID_59929 Human_SNP_ID_123758138 m1A Human chr3 - 15052501 15052501 15052501 GAAGGGCAGGTGCCCTGCCCCAGCCTGGTGCCATTACCCAAGGAGATGAGGGGGAAGTACAAAGC GAAGGGCAGGTGCCCTGCCCCAGCCTGGTGCCGTTACCCAAGGAGATGAGGGGGAAGTACAAAGC T C MRPS25 Ensembl:ENSG00000131368 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:15052451..15052525 26863196 MeRIP-seq:(Medium) rs771525885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592779,Human_RBP_ID_934856,Human_RBP_ID_17996745,Human_RBP_ID_18799614,Human_RBP_ID_19011567,Human_RBP_ID_19115120,Human_RBP_ID_22091491,Human_RBP_ID_22455340,Human_RBP_ID_22822488,Human_RBP_ID_23026469,Human_RBP_ID_23119959,Human_RBP_ID_26346240,Human_RBP_ID_27047560,Human_RBP_ID_27821959 59930 RMVar_ID_59930 Human_SNP_ID_123758375 m1A Human chr3 + 15053392 15053392 15053392 GGTCAAACCAAACAACTCACTCATTCTTCCCCAAGATTTTTCTGATGTGCTCCATGATCTCCTTA GGTCAAACCAAACAACTCACTCATTCTTCCCCCAGATTTTTCTGATGTGCTCCATGATCTCCTTA A C NR2C2 Ensembl:ENSG00000177463 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15053376..15053425 32194978 MeRIP-seq:(Medium) rs746509761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_398224 59931 RMVar_ID_59931 Human_SNP_ID_123758392 m1A Human chr3 - 15053429 15053429 15053429 GGGAGCAGGTCCTGGTGGATGTGGAGACCAAGAGCAATAAGGAGATCATGGAGCACATCAGAAAA GGGAGCAGGTCCTGGTGGATGTGGAGACCAAGGGCAATAAGGAGATCATGGAGCACATCAGAAAA T C MRPS25 Ensembl:ENSG00000131368 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15053341..15053478 26863196 MeRIP-seq:(Medium) rs1316194938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592782,Human_RBP_ID_1952476,Human_RBP_ID_7138032,Human_RBP_ID_14673889,Human_RBP_ID_18799620,Human_RBP_ID_22822491,Human_RBP_ID_23027165,Human_RBP_ID_23977522,Human_RBP_ID_25764266,Human_RBP_ID_27047568 Human_Splice_Rec_398240,Human_Splice_Rec_398241,Human_Splice_Rec_398246,Human_Splice_Rec_398247,Human_Splice_Rec_398252,Human_Splice_Rec_398262 59932 RMVar_ID_59932 Human_SNP_ID_123759975 m1A Human chr3 - 15059474 15059474 15059474 TTTCATAGGCTTCATTTCTTCCCTTTTGCAGGAAGTTTGTGTTTTTCAACATACCTCAGATTCAA TTTCATAGGCTTCATTTCTTCCCTTTTGCAGGCAGTTTGTGTTTTTCAACATACCTCAGATTCAA T G MRPS25 Ensembl:ENSG00000131368 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15059451..15059500 26863196 MeRIP-seq:(Medium) rs1367831861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67368 Human_Splice_Rec_398238,Human_Splice_Rec_398244,Human_Splice_Rec_398250,Human_Splice_Rec_398256,Human_Splice_Rec_398260 Human_miRNA_ID_2976337 RMVar_hsa_circ_216127,RMVar_hsa_circ_375605 59933 RMVar_ID_59933 Human_SNP_ID_123761941 m1A Human chr3 - 15065142 15065142 15065142 CCCCATCCGCCGCACCCTGCAATATCTGAGCCAGGGGAACGTGGTGTTCAAGGACTCCGTGAAGG CCCCATCCGCCGCACCCTGCAATATCTGAGCCGGGGGAACGTGGTGTTCAAGGACTCCGTGAAGG T C MRPS25 Ensembl:ENSG00000131368 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15065051..15065200 32194978 MeRIP-seq:(Medium) rs964335338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69863,Human_RBP_ID_592797,Human_RBP_ID_1620185,Human_RBP_ID_1952534,Human_RBP_ID_3963700,Human_RBP_ID_4757019,Human_RBP_ID_7138288,Human_RBP_ID_8562161,Human_RBP_ID_14674615,Human_RBP_ID_18423929,Human_RBP_ID_18799667,Human_RBP_ID_23977643,Human_RBP_ID_26823635 Human_Splice_Rec_398237,Human_Splice_Rec_398243,Human_Splice_Rec_398249,Human_Splice_Rec_398255,Human_Splice_Rec_398259 59934 RMVar_ID_59934 Human_SNP_ID_123762013 m1A Human chr3 - 15065260 15065260 15065260 GGGAGAAGCCGCGTGAGATCCGCGCGGGTGCTAGCTAGTCCTTTCTCGTCGCTGCTCGGCTCGCG GGGAGAAGCCGCGTGAGATCCGCGCGGGTGCTGGCTAGTCCTTTCTCGTCGCTGCTCGGCTCGCG T C MRPS25 Ensembl:ENSG00000131368 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15065067..15065325 26863196 MeRIP-seq:(Medium) rs569995490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757020,Human_RBP_ID_14674618 59935 RMVar_ID_59935 Human_SNP_ID_123762014 m1A Human chr3 - 15065260 15065260 15065260 GGGAGAAGCCGCGTGAGATCCGCGCGGGTGCTAGCTAGTCCTTTCTCGTCGCTGCTCGGCTCGCG GGGAGAAGCCGCGTGAGATCCGCGCGGGTGCTCGCTAGTCCTTTCTCGTCGCTGCTCGGCTCGCG T G MRPS25 Ensembl:ENSG00000131368 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15065067..15065325 26863196 MeRIP-seq:(Medium) rs569995490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757020,Human_RBP_ID_14674618 59936 RMVar_ID_59936 Human_SNP_ID_123763953 m1A Human chr3 - 15073726 15073726 15073726 GGGCCCAGGGGTCTGGCAGGAGCCAGTGGAGCAGGACAGAGGGCAGGCAGGATGGATGGGGAAGG GGGCCCAGGGGTCTGGCAGGAGCCAGTGGAGCGGGACAGAGGGCAGGCAGGATGGATGGGGAAGG T C RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:15073681..15073844 26863196 MeRIP-seq:(Medium) rs1339300536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4727621,Human_RBP_ID_7138428,Human_RBP_ID_14674887,Human_RBP_ID_22092231 Human_miRNA_ID_1094712 RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 59937 RMVar_ID_59937 Human_SNP_ID_123764262 m1A Human chr3 - 15074577 15074577 15074577 AGGCAGGCTGAGGAGGAGGACCTGCAGCGGGAACAGCTGCAGATGTTGCGTGAACGGGAGTTGGA AGGCAGGCTGAGGAGGAGGACCTGCAGCGGGAGCAGCTGCAGATGTTGCGTGAACGGGAGTTGGA T C RBSN Ensembl:ENSG00000131381 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:15074531..15074677 26863196 MeRIP-seq:(Medium) rs753402351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8868644,Human_RBP_ID_23977724 RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 59938 RMVar_ID_59938 Human_SNP_ID_123769976 m1A Human chr3 - 15098262 15098262 15098262 TGCTTCATTGTGTGTGCCAGGTACTGTGCTAAACCCTGGGGAGACGGCGAAGTGGAAAACATATA TGCTTCATTGTGTGTGCCAGGTACTGTGCTAAGCCCTGGGGAGACGGCGAAGTGGAAAACATATA T C RBSN Ensembl:ENSG00000131381 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:15098211..15098330 26863196 MeRIP-seq:(Medium) rs1156585953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757022,Human_RBP_ID_17151852 Human_Splice_Rec_398266,Human_Splice_Rec_398358 59939 RMVar_ID_59939 Human_SNP_ID_123769977 m1A Human chr3 - 15098263 15098263 15098263 CTGCTTCATTGTGTGTGCCAGGTACTGTGCTAAACCCTGGGGAGACGGCGAAGTGGAAAACATAT CTGCTTCATTGTGTGTGCCAGGTACTGTGCTAGACCCTGGGGAGACGGCGAAGTGGAAAACATAT T C RBSN Ensembl:ENSG00000131381 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15098230..15098318 26863196 MeRIP-seq:(Medium) rs977130513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4727705,Human_RBP_ID_17151852 Human_Splice_Rec_398266,Human_Splice_Rec_398358 59940 RMVar_ID_59940 Human_SNP_ID_123796929 m1A Human chr3 + 15206507 15206507 15206507 CCGGCGCGGGGCCACTGCGCCATGGACGCCACAGCACTGGAGCGGGACGCTGTGCAGTTCGCCCG CCGGCGCGGGGCCACTGCGCCATGGACGCCACGGCACTGGAGCGGGACGCTGTGCAGTTCGCCCG A G CAPN7 Ensembl:ENSG00000131375 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:15206476..15206525 26863196 MeRIP-seq:(Medium) rs1361216313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757785,Human_RBP_ID_8874841,Human_RBP_ID_9302132,Human_RBP_ID_22091499,Human_RBP_ID_23026321 Human_Splice_Rec_398423,Human_Splice_Rec_398429,Human_Splice_Rec_398435 RMVar_hsa_circ_84590,RMVar_hsa_circ_216138 59941 RMVar_ID_59941 Human_SNP_ID_123810250 m1A Human chr3 + 15255377 15255377 15255377 GATAAGGCTTATGCTGTAGAACCTTCTCCCCCACAGCCACAAATCCCCTTCTATAAGTCCCTCCT GATAAGGCTTATGCTGTAGAACCTTCTCCCCCCCAGCCACAAATCCCCTTCTATAAGTCCCTCCT A C SH3BP5-AS1 Ensembl:ENSG00000224660 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:15255326..15255489;chr3:15255327..15255475 26863196 MeRIP-seq:(Medium) rs375639263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5102075,Human_RBP_ID_14679652,Human_RBP_ID_17088517,Human_RBP_ID_18799928 59942 RMVar_ID_59942 Human_SNP_ID_123810839 m1A Human chr3 - 15256952 15256952 15256952 CGGTTGTGAGGCCTGGCAGCCTGGATCTGCCCAGCCCTGTGTCCCTGTCAGAGTTTGGGATGATG CGGTTGTGAGGCCTGGCAGCCTGGATCTGCCCCGCCCTGTGTCCCTGTCAGAGTTTGGGATGATG T G SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15256904..15257052 26863196 MeRIP-seq:(Medium) rs755431705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_398553,Human_Splice_Rec_398559,Human_Splice_Rec_398579,Human_Splice_Rec_398595 59943 RMVar_ID_59943 Human_SNP_ID_123810903 m1A Human chr3 + 15257084 15257084 15257084 TTCCGAGTCATCTTCAGACACAAAGTTGCTACAGCTGTCATCTTCAAAGGCCTCCGAGGCCACTA TTCCGAGTCATCTTCAGACACAAAGTTGCTACGGCTGTCATCTTCAAAGGCCTCCGAGGCCACTA A G SH3BP5-AS1 Ensembl:ENSG00000224660 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:15257034..15259000 32194978 MeRIP-seq:(Medium) rs748728890 Functional Loss SNV dbSNP153 33..33 33 - - - 59944 RMVar_ID_59944 Human_SNP_ID_123811506 m1A Human chr3 - 15258989 15258989 15258989 GGCCAAACTGACCCTGGCAAAAGGCGAGTACAAGATGGCCCTGAAGAACCTGGAGATGATCTCAG GGCCAAACTGACCCTGGCAAAAGGCGAGTACAGGATGGCCCTGAAGAACCTGGAGATGATCTCAG T C SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15258793..15259052 26863196 MeRIP-seq:(Medium) rs754656049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1031597,Human_RBP_ID_4728119,Human_RBP_ID_14679780,Human_RBP_ID_18446148 Human_Splice_Rec_398550,Human_Splice_Rec_398576,Human_Splice_Rec_398592,Human_Splice_Rec_398604 Human_miRNA_ID_2352857,Human_miRNA_ID_2572278 RMVar_hsa_circ_216169,RMVar_hsa_circ_45131,RMVar_hsa_circ_64757,RMVar_hsa_circ_369940,RMVar_hsa_circ_12976 59945 RMVar_ID_59945 Human_SNP_ID_123812496 m1A Human chr3 - 15262205 15262205 15262205 CGGCAGCCAGGTACAATGCCGCCATGGGCCGCATGCGACAGCTGGAGAAGAAACTCAAGAGAGCC CGGCAGCCAGGTACAATGCCGCCATGGGCCGCGTGCGACAGCTGGAGAAGAAACTCAAGAGAGCC T C SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15262110..15262334 26863196 MeRIP-seq:(Medium) rs145105347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593192,Human_RBP_ID_5207858 Human_Splice_Rec_398546,Human_Splice_Rec_398547,Human_Splice_Rec_398572,Human_Splice_Rec_398573,Human_Splice_Rec_398588,Human_Splice_Rec_398589,Human_Splice_Rec_398600,Human_Splice_Rec_398601,Human_Splice_Rec_398612,Human_Splice_Rec_398618 RMVar_hsa_circ_216169,RMVar_hsa_circ_64757,RMVar_hsa_circ_369940,RMVar_hsa_circ_12976,RMVar_hsa_circ_7259,RMVar_hsa_circ_117334,RMVar_hsa_circ_216170,RMVar_hsa_circ_216171 59946 RMVar_ID_59946 Human_SNP_ID_123812509 m1A Human chr3 - 15262233 15262233 15262233 ACCAGGAGCGAGCTGGTGCATAAGGAGACGGCAGCCAGGTACAATGCCGCCATGGGCCGCATGCG ACCAGGAGCGAGCTGGTGCATAAGGAGACGGCCGCCAGGTACAATGCCGCCATGGGCCGCATGCG T G SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:15262162..15271606 32194978 MeRIP-seq:(Medium) rs1413358884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593192 Human_Splice_Rec_398546,Human_Splice_Rec_398547,Human_Splice_Rec_398572,Human_Splice_Rec_398573,Human_Splice_Rec_398588,Human_Splice_Rec_398589,Human_Splice_Rec_398600,Human_Splice_Rec_398601,Human_Splice_Rec_398612,Human_Splice_Rec_398618 Human_miRNA_ID_2330484,Human_miRNA_ID_2963564 RMVar_hsa_circ_216169,RMVar_hsa_circ_64757,RMVar_hsa_circ_369940,RMVar_hsa_circ_12976,RMVar_hsa_circ_7259,RMVar_hsa_circ_117334,RMVar_hsa_circ_216170,RMVar_hsa_circ_216171 59947 RMVar_ID_59947 Human_SNP_ID_123814469 m1A Human chr3 + 15269673 15269673 15269673 TACCTCCGCTCAGGGGAAGCCAGCGCGCATGCACGCGCACACCCCCACAGCACACCCGGCCATGA TACCTCCGCTCAGGGGAAGCCAGCGCGCATGCGCGCGCACACCCCCACAGCACACCCGGCCATGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15269670..15269920 26863196 MeRIP-seq:(Medium) rs769380338 Functional Loss SNV dbSNP153 33..33 33 - - - 59948 RMVar_ID_59948 Human_SNP_ID_123814476 m1A Human chr3 + 15269679 15269679 15269679 CGCTCAGGGGAAGCCAGCGCGCATGCACGCGCACACCCCCACAGCACACCCGGCCATGACTCATA CGCTCAGGGGAAGCCAGCGCGCATGCACGCGCCCACCCCCACAGCACACCCGGCCATGACTCATA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15269676..15269918 26863196 MeRIP-seq:(Medium) rs767987327 Functional Loss SNV dbSNP153 33..33 33 - - - 59949 RMVar_ID_59949 Human_SNP_ID_123817327 m1A Human chr3 - 15280600 15280600 15280600 TGATGTCGGGGATGGCTGTGTGGCTGGCTGGCAGGGAAGGCAGCTTGGATTGGGGCTGATAGAAT TGATGTCGGGGATGGCTGTGTGGCTGGCTGGCGGGGAAGGCAGCTTGGATTGGGGCTGATAGAAT T C SH3BP5 Ensembl:ENSG00000131370 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:15280598..15280846;chr3:15280596..15280789 26863196 MeRIP-seq:(Medium) rs990693418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216169,RMVar_hsa_circ_369940,RMVar_hsa_circ_315080 59950 RMVar_ID_59950 Human_SNP_ID_123823236 m1A Human chr3 - 15304196 15304196 15304196 GCTCGTCAGAAGTTCCGCTCTGTTCTGGTTGAAGCAACGGTGAAACTGGATGAACTGGTGAAGAA GCTCGTCAGAAGTTCCGCTCTGTTCTGGTTGAGGCAACGGTGAAACTGGATGAACTGGTGAAGAA T C SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15304063..15304272 26863196 MeRIP-seq:(Medium) rs765227528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18799977,Human_RBP_ID_26347798,Human_RBP_ID_27821975 Human_Splice_Rec_398542,Human_Splice_Rec_398543,Human_Splice_Rec_398564,Human_Splice_Rec_398565,Human_Splice_Rec_398585,Human_Splice_Rec_398609,Human_Splice_Rec_398622,Human_Splice_Rec_398623,Human_Splice_Rec_398630 Human_miRNA_ID_2069576,Human_miRNA_ID_2802475 RMVar_hsa_circ_216169,RMVar_hsa_circ_369940,RMVar_hsa_circ_315080 59951 RMVar_ID_59951 Human_SNP_ID_123830319 m1A Human chr3 - 15332335 15332335 15332335 CGAAATCCTGCCGCCTGCCCGGGACGAGGAGGAGGAGGAGGAAGAGGGGATGGAGCAGGGGCTGG CGAAATCCTGCCGCCTGCCCGGGACGAGGAGGTGGAGGAGGAAGAGGGGATGGAGCAGGGGCTGG T A SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:15332227..15332575;chr3:15332219..15332575;chr3:15332220..15332575 26863196 MeRIP-seq:(Medium) rs1172620358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593198,Human_RBP_ID_3963708,Human_RBP_ID_5149885,Human_RBP_ID_26347800,Human_RBP_ID_27821976 Human_Splice_Rec_398539,Human_Splice_Rec_398555,Human_Splice_Rec_398605 59952 RMVar_ID_59952 Human_SNP_ID_123830339 m1A Human chr3 - 15332377 15332377 15332377 CATGGACGCGGCACTGAAGCGGAGCCGCTCGGAGGAGCCAGCCGAAATCCTGCCGCCTGCCCGGG CATGGACGCGGCACTGAAGCGGAGCCGCTCGGGGGAGCCAGCCGAAATCCTGCCGCCTGCCCGGG T C SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:15332326..15332550 26863196 MeRIP-seq:(Medium) rs1180399165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785303,Human_RBP_ID_4728135 59953 RMVar_ID_59953 Human_SNP_ID_123857596 m1A Human chr3 + 15442323 15442323 15442323 TAATGTTATATACAGCCAAAGTGGATGTTTCTATTTGGCAAGGAAGGTAGGATTTCTGAAACTCA TAATGTTATATACAGCCAAAGTGGATGTTTCTGTTTGGCAAGGAAGGTAGGATTTCTGAAACTCA A G EAF1 Ensembl:ENSG00000144597 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593364,Human_RBP_ID_1953191,Human_RBP_ID_5149887,Human_RBP_ID_5654278,Human_RBP_ID_7141744,Human_RBP_ID_8949695,Human_RBP_ID_14683352,Human_RBP_ID_17291242,Human_RBP_ID_17997348,Human_RBP_ID_18334137,Human_RBP_ID_21897917,Human_RBP_ID_23978876,Human_RBP_ID_26504828,Human_RBP_ID_27713796 Human_miRNA_ID_824029,Human_miRNA_ID_2349353 GWAS_ID_7055,GWAS_ID_7056,GWAS_ID_7057,GWAS_ID_7058,GWAS_ID_7059,GWAS_ID_7060,GWAS_ID_7061,GWAS_ID_7062,GWAS_ID_7063,GWAS_ID_7064,GWAS_ID_7065,GWAS_ID_7066,GWAS_ID_7067 RMVar_hsa_circ_86821,RMVar_hsa_circ_97003,RMVar_hsa_circ_216180,RMVar_hsa_circ_216184,RMVar_hsa_circ_216185,RMVar_hsa_circ_83713 59954 RMVar_ID_59954 Human_SNP_ID_123860146 m1A Human chr3 + 15453007 15453007 15453007 GGACAGAAGAGATCGGAAGCACCAGTAGATCCACTCTGGAACCCAGTGAAGAGCAGGGCATGGCC GGACAGAAGAGATCGGAAGCACCAGTAGATCCTCTCTGGAACCCAGTGAAGAGCAGGGCATGGCC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:15452900..15453032 26863196 MeRIP-seq:(Medium) rs1049076646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14683434 59955 RMVar_ID_59955 Human_SNP_ID_123888339 m1A Human chr3 + 15569529 15569529 15569529 AACATGGTGAAATCCTGTCTCTACTAAAAAAAATACAAAAATTGGCTGGGTGCGGTGGCTCACGC AACATGGTGAAATCCTGTCTCTACTAAAAAAAGTACAAAAATTGGCTGGGTGCGGTGGCTCACGC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:15569512..15569603 26863410 MeRIP-seq:(Medium) rs1394923314 Functional Loss SNV dbSNP153 33..33 33 - - - 59956 RMVar_ID_59956 Human_SNP_ID_123897885 m1A Human chr3 + 15601801 15601801 15601801 AGGTAAGAAGCCGAACTCTGAGGCCTCTCGCCATTGTCTCCGAGTCGGCCAGCTGGAGCGTTTTC AGGTAAGAAGCCGAACTCTGAGGCCTCTCGCCGTTGTCTCCGAGTCGGCCAGCTGGAGCGTTTTC A G BTD Ensembl:ENSG00000169814 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15601764..15601894 26863196 MeRIP-seq:(Medium) rs1265479087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4728860,Human_RBP_ID_5505760,Human_RBP_ID_18423931 Human_Splice_Rec_399191,Human_Splice_Rec_399197,Human_Splice_Rec_399199,Human_Splice_Rec_399207,Human_Splice_Rec_399211,Human_Splice_Rec_399215,Human_Splice_Rec_399219,Human_Splice_Rec_399231,Human_Splice_Rec_399245,Human_Splice_Rec_399251,Human_Splice_Rec_399255,Human_Splice_Rec_399259 59957 RMVar_ID_59957 Human_SNP_ID_123897935 m1A Human chr3 - 15601865 15601865 15601865 TACCTGCTCTTAGCGCGCCTTCCGCCCTGAATATGCGCATGCGCCATTCTCCCTTTACAGCCCCG TACCTGCTCTTAGCGCGCCTTCCGCCCTGAATGTGCGCATGCGCCATTCTCCCTTTACAGCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:15601767..15601946;chr3:15601787..15601936 26863196 MeRIP-seq:(Medium) rs374044613 Functional Loss SNV dbSNP153 33..33 33 - - - 59958 RMVar_ID_59958 Human_SNP_ID_123906194 m1A Human chr3 - 15635498 15635496 15635498 CAGCCACGCTCTCCTCCCCGGTGTGGGCTCCCAGGGCAACCACGTAACAGCCGCAGAGGAAAAGA CAGCCACGCTCTCCTCCCCGGTGTGGGCTCCC__GGCAACCACGTAACAGCCGCAGAGGAAAAGA CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15635406..15635628 26863196 MeRIP-seq:(Medium) rs1553652080 Functional Loss DEL dbSNP153 33..34 33 - - - Clinvar_Rec_201 59959 RMVar_ID_59959 Human_SNP_ID_123906231 m1A Human chr3 + 15635577 15635577 15635577 GAATATTATGTGGCTGCCGTGTATGAGCATCCATCCATCCTGAGTCTGAACCCTCTGGCTCTCAT GAATATTATGTGGCTGCCGTGTATGAGCATCCGTCCATCCTGAGTCTGAACCCTCTGGCTCTCAT A G BTD Ensembl:ENSG00000169814 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15635528..15635628 32194978 MeRIP-seq:(Medium) rs1159185297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87295,RMVar_hsa_circ_216208,RMVar_hsa_circ_343916,RMVar_hsa_circ_68742 59960 RMVar_ID_59960 Human_SNP_ID_123908707 m1A Human chr3 - 15644437 15644434 15644437 TTCCATTATTGCTGAACACGACATTTGTGTTGAACTGGTATCTCCCATCTTTTGGGCACCTTGGG TTCCATTATTGCTGAACACGACATTTGTGTTG___TGGTATCTCCCATCTTTTGGGCACCTTGGG AGTT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15644340..15644440 32194978 MeRIP-seq:(Medium) rs781696450 Functional Loss DEL dbSNP153 33..35 33 - - - 59961 RMVar_ID_59961 Human_SNP_ID_123909200 m1A Human chr3 + 15645424 15645424 15645424 TGGCTGGGAGAATGACCACTATTTCCTGAGGAAAAGTAGGCTGTCCTCTGGGCTGGTGACGGCGG TGGCTGGGAGAATGACCACTATTTCCTGAGGAGAAGTAGGCTGTCCTCTGGGCTGGTGACGGCGG A G BTD Ensembl:ENSG00000169814 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15645179..15645427 32194978 MeRIP-seq:(Medium) rs370021134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17402304 Human_miRNA_ID_2997664 RMVar_hsa_circ_87295,RMVar_hsa_circ_216208 59962 RMVar_ID_59962 Human_SNP_ID_123943768 m1A Human chr3 - 15785364 15785364 15785364 CGTTTTTTAAACAGGTTTGTGTTCTTCTGGTTAGGTTTTGGGATTTCTTTGTAGATTTTGGATAA CGTTTTTTAAACAGGTTTGTGTTCTTCTGGTTTGGTTTTGGGATTTCTTTGTAGATTTTGGATAA T A ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:15785354..15785438 26863196 MeRIP-seq:(Medium) rs1378306178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18800801 RMVar_hsa_circ_100377,RMVar_hsa_circ_216231,RMVar_hsa_circ_94219,RMVar_hsa_circ_216232,RMVar_hsa_circ_216241,RMVar_hsa_circ_62922,RMVar_hsa_circ_374760,RMVar_hsa_circ_216240,RMVar_hsa_circ_335396,RMVar_hsa_circ_311599,RMVar_hsa_circ_85117,RMVar_hsa_circ_216250,RMVar_hsa_circ_216253,RMVar_hsa_circ_216251,RMVar_hsa_circ_291183,RMVar_hsa_circ_326322,RMVar_hsa_circ_216252,RMVar_hsa_circ_216255,RMVar_hsa_circ_302918,RMVar_hsa_circ_316673,RMVar_hsa_circ_216254 59963 RMVar_ID_59963 Human_SNP_ID_123961869 m1A Human chr3 - 15859435 15859435 15859435 GTCGGCGGCGGCAGCGGCAGCGGCGGAGGAGGAGGAGGCTGGAGTGGGCGCGGAGGCGACCGCCA GTCGGCGGCGGCAGCGGCAGCGGCGGAGGAGGGGGAGGCTGGAGTGGGCGCGGAGGCGACCGCCA T C ANKRD28 Ensembl:ENSG00000206560 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:15859310..15859562 26863196 MeRIP-seq:(Medium) rs1434001432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247972,Human_RBP_ID_3963712,Human_RBP_ID_4729245,Human_RBP_ID_9434822,Human_RBP_ID_18194503,Human_RBP_ID_18424401,Human_RBP_ID_19011577,Human_RBP_ID_23026590,Human_RBP_ID_26790555 Human_Splice_Rec_399339,Human_Splice_Rec_399393,Human_Splice_Rec_399625 Human_miRNA_ID_2972573,Human_miRNA_ID_3005759 RMVar_hsa_circ_100377,RMVar_hsa_circ_216231 59964 RMVar_ID_59964 Human_SNP_ID_123961887 m1A Human chr3 - 15859455 15859452 15859455 GGGGCGGGAGCAGTGGGCCGGTCGGCGGCGGCAGCGGCAGCGGCGGAGGAGGAGGAGGCTGGAGT GGGGCGGGAGCAGTGGGCCGGTCGGCGGCGGC___GGCAGCGGCGGAGGAGGAGGAGGCTGGAGT CGCT C ANKRD28 Ensembl:ENSG00000206560 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:15859296..15859538 26863196 MeRIP-seq:(Medium) rs562111487 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_836568,Human_RBP_ID_3964804,Human_RBP_ID_4756332,Human_RBP_ID_5390557,Human_RBP_ID_9434822,Human_RBP_ID_18194503,Human_RBP_ID_18424401,Human_RBP_ID_19011577,Human_RBP_ID_23026590,Human_RBP_ID_26790555 Human_Splice_Rec_399339,Human_Splice_Rec_399393,Human_Splice_Rec_399625 RMVar_hsa_circ_100377,RMVar_hsa_circ_216231 59965 RMVar_ID_59965 Human_SNP_ID_123961892 m1A Human chr3 - 15859455 15859455 15859455 GGGGCGGGAGCAGTGGGCCGGTCGGCGGCGGCAGCGGCAGCGGCGGAGGAGGAGGAGGCTGGAGT GGGGCGGGAGCAGTGGGCCGGTCGGCGGCGGCGGCGGCAGCGGCGGAGGAGGAGGAGGCTGGAGT T C ANKRD28 Ensembl:ENSG00000206560 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:15859296..15859538 26863196 MeRIP-seq:(Medium) rs1342279486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836568,Human_RBP_ID_3964804,Human_RBP_ID_4756332,Human_RBP_ID_5390557,Human_RBP_ID_9434822,Human_RBP_ID_18194503,Human_RBP_ID_18424401,Human_RBP_ID_19011577,Human_RBP_ID_23026590,Human_RBP_ID_26790555 Human_Splice_Rec_399339,Human_Splice_Rec_399393,Human_Splice_Rec_399625 RMVar_hsa_circ_100377,RMVar_hsa_circ_216231 59966 RMVar_ID_59966 Human_SNP_ID_123962033 m1A Human chr3 - 15859748 15859748 15859748 TGGAACGGCGCGGCCGCGGGGGCTGCCAGGGTATTTCGGGAAGGGGGCGTGAGGAGGCGGCGGCG TGGAACGGCGCGGCCGCGGGGGCTGCCAGGGTGTTTCGGGAAGGGGGCGTGAGGAGGCGGCGGCG T C ANKRD28 Ensembl:ENSG00000206560 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:15859690..15859775 26863410 MeRIP-seq:(Medium) rs1470463148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70458,Human_RBP_ID_282495,Human_RBP_ID_4762382,Human_RBP_ID_9354309,Human_RBP_ID_18423932 59967 RMVar_ID_59967 Human_SNP_ID_123962271 m1A Human chr3 - 15860235 15860235 15860235 ACGCTTTCTCCACGTGCAAGTCCGGCTCGCCCATCGCCACTCGCCGCAGCCCCCAGGTGCCCACC ACGCTTTCTCCACGTGCAAGTCCGGCTCGCCCCTCGCCACTCGCCGCAGCCCCCAGGTGCCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:15860136..15860341 26863196 MeRIP-seq:(Medium) rs1161946441 Functional Loss SNV dbSNP153 33..33 33 - - - 59968 RMVar_ID_59968 Human_SNP_ID_124057329 m1A Human chr3 - 16259118 16259118 16259118 CTCACTCACTATGGTGGCATCAGCTGCAAAGCAAAATGAACTGTCCCATGATCATGTTGATGGTT CTCACTCACTATGGTGGCATCAGCTGCAAAGCGAAATGAACTGTCCCATGATCATGTTGATGGTT T C DPH3 Ensembl:ENSG00000154813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs842254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8869319 GWAS_ID_7068,GWAS_ID_7069,GWAS_ID_7070,GWAS_ID_7071,GWAS_ID_7072,GWAS_ID_7073,GWAS_ID_7074,GWAS_ID_7075,GWAS_ID_7076,GWAS_ID_7077,GWAS_ID_7078,GWAS_ID_7079,GWAS_ID_7080,GWAS_ID_7081,GWAS_ID_7082,GWAS_ID_7083,GWAS_ID_7084,GWAS_ID_7085,GWAS_ID_7086,GWAS_ID_7087,GWAS_ID_7088,GWAS_ID_7089,GWAS_ID_7090,GWAS_ID_7091,GWAS_ID_7092,GWAS_ID_7093,GWAS_ID_7094,GWAS_ID_7095,GWAS_ID_7096,GWAS_ID_7097,GWAS_ID_7098,GWAS_ID_7099,GWAS_ID_7100,GWAS_ID_7101,GWAS_ID_7102,GWAS_ID_7103,GWAS_ID_7104,GWAS_ID_7105,GWAS_ID_7106,GWAS_ID_7107,GWAS_ID_7108,GWAS_ID_7109,GWAS_ID_7110,GWAS_ID_7111,GWAS_ID_7112,GWAS_ID_7113,GWAS_ID_7114,GWAS_ID_7115,GWAS_ID_7116,GWAS_ID_7117,GWAS_ID_7118,GWAS_ID_7119,GWAS_ID_7120,GWAS_ID_7121,GWAS_ID_7122,GWAS_ID_7123,GWAS_ID_7124,GWAS_ID_7125,GWAS_ID_7126,GWAS_ID_7127,GWAS_ID_7128,GWAS_ID_7129,GWAS_ID_7130,GWAS_ID_7131,GWAS_ID_7132,GWAS_ID_7133,GWAS_ID_7134,GWAS_ID_7135,GWAS_ID_7136,GWAS_ID_7137,GWAS_ID_7138,GWAS_ID_7139,GWAS_ID_7140,GWAS_ID_7141,GWAS_ID_7142,GWAS_ID_7143,GWAS_ID_7144,GWAS_ID_7145,GWAS_ID_7146,GWAS_ID_7147,GWAS_ID_7148,GWAS_ID_7149,GWAS_ID_7150,GWAS_ID_7151,GWAS_ID_7152,GWAS_ID_7153,GWAS_ID_7154,GWAS_ID_7155,GWAS_ID_7156,GWAS_ID_7157,GWAS_ID_7158,GWAS_ID_7159,GWAS_ID_7160,GWAS_ID_7161,GWAS_ID_7162,GWAS_ID_7163,GWAS_ID_7164,GWAS_ID_7165,GWAS_ID_7166,GWAS_ID_7167,GWAS_ID_7168,GWAS_ID_7169,GWAS_ID_7170,GWAS_ID_7171,GWAS_ID_7172,GWAS_ID_7173,GWAS_ID_7174,GWAS_ID_7175,GWAS_ID_7176,GWAS_ID_7177,GWAS_ID_7178,GWAS_ID_7179,GWAS_ID_7180,GWAS_ID_7181,GWAS_ID_7182,GWAS_ID_7183,GWAS_ID_7184,GWAS_ID_7185,GWAS_ID_7186,GWAS_ID_7187,GWAS_ID_7188,GWAS_ID_7189,GWAS_ID_7190,GWAS_ID_7191,GWAS_ID_7192,GWAS_ID_7193,GWAS_ID_7194,GWAS_ID_7195,GWAS_ID_7196,GWAS_ID_7197,GWAS_ID_7198,GWAS_ID_7199,GWAS_ID_7200,GWAS_ID_7201,GWAS_ID_7202,GWAS_ID_7203,GWAS_ID_7204,GWAS_ID_7205,GWAS_ID_7206,GWAS_ID_7207,GWAS_ID_7208,GWAS_ID_7209,GWAS_ID_7210,GWAS_ID_7211,GWAS_ID_7212,GWAS_ID_7213,GWAS_ID_7214,GWAS_ID_7215,GWAS_ID_7216,GWAS_ID_7217,GWAS_ID_7218,GWAS_ID_7219,GWAS_ID_7220,GWAS_ID_7221,GWAS_ID_7222,GWAS_ID_7223,GWAS_ID_7224,GWAS_ID_7225,GWAS_ID_7226,GWAS_ID_7227,GWAS_ID_7228,GWAS_ID_7229,GWAS_ID_7230,GWAS_ID_7231,GWAS_ID_7232,GWAS_ID_7233,GWAS_ID_7234,GWAS_ID_7235,GWAS_ID_7236,GWAS_ID_7237,GWAS_ID_7238,GWAS_ID_7239,GWAS_ID_7240,GWAS_ID_7241,GWAS_ID_7242,GWAS_ID_7243,GWAS_ID_7244,GWAS_ID_7245,GWAS_ID_7246,GWAS_ID_7247,GWAS_ID_7248,GWAS_ID_7249,GWAS_ID_7250,GWAS_ID_7251,GWAS_ID_7252,GWAS_ID_7253,GWAS_ID_7254,GWAS_ID_7255,GWAS_ID_7256,GWAS_ID_7257,GWAS_ID_7258,GWAS_ID_7259,GWAS_ID_7260,GWAS_ID_7261 59969 RMVar_ID_59969 Human_SNP_ID_124063021 m1A Human chr3 + 16282619 16282619 16282619 GAGGGAGGACCTCAGGCAGGGGGTGTTACTTGAGCAGGGCCTAGAAGGGTGAGCAGAAGGTTGGT GAGGGAGGACCTCAGGCAGGGGGTGTTACTTGGGCAGGGCCTAGAAGGGTGAGCAGAAGGTTGGT A G OXNAD1 Ensembl:ENSG00000154814 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:16282591..16282780 26863196 MeRIP-seq:(Medium) rs189602932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7150214 RMVar_hsa_circ_56367,RMVar_hsa_circ_362386,RMVar_hsa_circ_364589,RMVar_hsa_circ_344861,RMVar_hsa_circ_216267,RMVar_hsa_circ_353961,RMVar_hsa_circ_32637 59970 RMVar_ID_59970 Human_SNP_ID_124063561 m1A Human chr3 - 16285050 16285050 16285050 CTCCTAAAAATCAACTGGGGTAATTTTCCATTACTGACCCTCTACCTGCACTCTTGGTCCTAGTC CTCCTAAAAATCAACTGGGGTAATTTTCCATTTCTGACCCTCTACCTGCACTCTTGGTCCTAGTC T A lnc-DPH3-3 RNACentral:URS00008BD176 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:16285008..16285126 26863196 MeRIP-seq:(Medium) rs1488291448 Functional Loss SNV dbSNP153 33..33 33 - - - 59971 RMVar_ID_59971 Human_SNP_ID_124121100 m1A Human chr3 - 16513516 16513516 16513516 TCCTCCCCGCGCCGCCTCCTCTGTATGGCACAAACTTTCCTCCCGGGACGGAACACGCTGCCTCA TCCTCCCCGCGCCGCCTCCTCTGTATGGCACAGACTTTCCTCCCGGGACGGAACACGCTGCCTCA T C RFTN1 Ensembl:ENSG00000131378 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:16513466..16513736 26863196 MeRIP-seq:(Medium) rs960195108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_399851,Human_Splice_Rec_399921 59972 RMVar_ID_59972 Human_SNP_ID_124212790 m1A Human chr3 - 16885359 16885359 16885359 CGATGAGCGCCCTTCTCCCACCTACCTTGATGATGCTGCTCCGGCGGGGCAGGCCGCCCGGCTTG CGATGAGCGCCCTTCTCCCACCTACCTTGATGTTGCTGCTCCGGCGGGGCAGGCCGCCCGGCTTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:16885259..16885375 26863410 MeRIP-seq:(Medium) rs1482169508 Functional Loss SNV dbSNP153 33..33 33 - - - 59973 RMVar_ID_59973 Human_SNP_ID_124233567 m1A Human chr3 + 16974256 16974256 16974256 GGAAAACGTTAAAGAGTTTTAAGCAGGCAGGAATCAAAATCGGGTCTCACAGCTGCAGTGGAAAG GGAAAACGTTAAAGAGTTTTAAGCAGGCAGGACTCAAAATCGGGTCTCACAGCTGCAGTGGAAAG A C PLCL2 Ensembl:ENSG00000154822 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:16974250..16974455 26863196 MeRIP-seq:(Medium) rs890371151 Functional Loss SNV dbSNP153 33..33 33 - - - 59974 RMVar_ID_59974 Human_SNP_ID_124258559 m1A Human chr3 + 17083287 17083287 17083287 AGAGTCAAGATGGCATCAAGGGGAGGGGAAGGAGCTAGCTACGTGCATTTCTGGGGCAAGGGCAT AGAGTCAAGATGGCATCAAGGGGAGGGGAAGGTGCTAGCTACGTGCATTTCTGGGGCAAGGGCAT A T PLCL2 Ensembl:ENSG00000154822 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:17083067..17083534 26863196 MeRIP-seq:(Medium) rs1424359461 Functional Loss SNV dbSNP153 33..33 33 - - - 59975 RMVar_ID_59975 Human_SNP_ID_124278583 m1A Human chr3 - 17161098 17161098 17161098 CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCAGTCTGCTCCCCACTGGTGTTCTCAGATCCACT CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCTGTCTGCTCCCCACTGGTGTTCTCAGATCCACT T A TBC1D5 Ensembl:ENSG00000131374 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:17161050..17161151 32194978 MeRIP-seq:(Medium) rs985203162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27499929 Human_miRNA_ID_2366170,Human_miRNA_ID_2366171,Human_miRNA_ID_2724956,Human_miRNA_ID_2724957,Human_miRNA_ID_3013978,Human_miRNA_ID_3013979 RMVar_hsa_circ_109601,RMVar_hsa_circ_118271,RMVar_hsa_circ_115931,RMVar_hsa_circ_216297,RMVar_hsa_circ_216299,RMVar_hsa_circ_85797,RMVar_hsa_circ_216298,RMVar_hsa_circ_216296 59976 RMVar_ID_59976 Human_SNP_ID_124278584 m1A Human chr3 - 17161098 17161098 17161098 CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCAGTCTGCTCCCCACTGGTGTTCTCAGATCCACT CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCCGTCTGCTCCCCACTGGTGTTCTCAGATCCACT T G TBC1D5 Ensembl:ENSG00000131374 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:17161050..17161151 32194978 MeRIP-seq:(Medium) rs985203162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27499929 Human_miRNA_ID_2366170,Human_miRNA_ID_2366171,Human_miRNA_ID_2724956,Human_miRNA_ID_2724957,Human_miRNA_ID_3013978,Human_miRNA_ID_3013979 RMVar_hsa_circ_109601,RMVar_hsa_circ_118271,RMVar_hsa_circ_115931,RMVar_hsa_circ_216297,RMVar_hsa_circ_216299,RMVar_hsa_circ_85797,RMVar_hsa_circ_216298,RMVar_hsa_circ_216296 59977 RMVar_ID_59977 Human_SNP_ID_124409966 m1A Human chr3 + 17699976 17699976 17699976 AAATGCTCTGCCCCCTGAGATATACCCCCTTCACCTGTTAGAAGCTCCTTCCTTGTCCACTTATG AAATGCTCTGCCCCCTGAGATATACCCCCTTCCCCTGTTAGAAGCTCCTTCCTTGTCCACTTATG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:17699927..17700027 26863196 MeRIP-seq:(Medium) rs1455408813 Functional Loss SNV dbSNP153 33..33 33 - - - 59978 RMVar_ID_59978 Human_SNP_ID_124585621 m1A Human chr3 - 18425146 18425138 18425147 CCCACAGCGGCAGCGGCGGCGGCGGCGGCAGCAGCAGCAGGAGCAGCGGCGGAGAGGGCTGCAGC CCCACAGCGGCAGCGGCGGCGGCGGCGGCAG_________GAGCAGCGGCGGAGAGGGCTGCAGC CCTGCTGCTG C TBC1D5,SATB1 Ensembl:ENSG00000131374,Ensembl:ENSG00000182568 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:18425039..18425315 26863196 MeRIP-seq:(Medium) rs1287358635 Functional Loss DEL dbSNP153 32..40 33 - - - Human_Splice_Rec_400653 RMVar_hsa_circ_268436 59979 RMVar_ID_59979 Human_SNP_ID_124585622 m1A Human chr3 - 18425146 18425138 18425147 CCCACAGCGGCAGCGGCGGCGGCGGCGGCAGCAGCAGCAGGAGCAGCGGCGGAGAGGGCTGCAGC CCCACAGCGGCAGCGGCGGCGGCGGCGGCAG___CAGCAGGAGCAGCGGCGGAGAGGGCTGCAGC CCTGCTGCTG CCTGCTG TBC1D5,SATB1 Ensembl:ENSG00000131374,Ensembl:ENSG00000182568 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:18425039..18425315 26863196 MeRIP-seq:(Medium) rs1287358635 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_400653 RMVar_hsa_circ_268436 59980 RMVar_ID_59980 Human_SNP_ID_124585626 m1A Human chr3 - 18425146 18425146 18425146 CCCACAGCGGCAGCGGCGGCGGCGGCGGCAGCAGCAGCAGGAGCAGCGGCGGAGAGGGCTGCAGC CCCACAGCGGCAGCGGCGGCGGCGGCGGCAGCGGCAGCAGGAGCAGCGGCGGAGAGGGCTGCAGC T C TBC1D5,SATB1 Ensembl:ENSG00000131374,Ensembl:ENSG00000182568 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:18425039..18425315 26863196 MeRIP-seq:(Medium) rs933754142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_400653 RMVar_hsa_circ_268436 59981 RMVar_ID_59981 Human_SNP_ID_124969655 m1A Human chr3 + 19947256 19947256 19947256 CAGAGGGAGGAGGAGGAGGAAGAATTAGTCGGAACTCCAGCGCCGGCGGCGGCGGCGGCGGCGGA CAGAGGGAGGAGGAGGAGGAAGAATTAGTCGGCACTCCAGCGCCGGCGGCGGCGGCGGCGGCGGA A C RAB5A Ensembl:ENSG00000144566 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:19947093..19947500;chr3:19947094..19947500 26863196 MeRIP-seq:(Medium) rs563651436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4737640,Human_RBP_ID_8943466 59982 RMVar_ID_59982 Human_SNP_ID_124969756 m1A Human chr3 + 19947390 19947382 19947390 GGCACGAGCCCCGCACAGTCCAGTGTGAGGGGAGCGGCGCTAAGAGCAGGCGACGCCGCCGCCGC GGCACGAGCCCCGCACAGTCCAGTG________GCGGCGCTAAGAGCAGGCGACGCCGCCGCCGC GTGAGGGGA G RAB5A Ensembl:ENSG00000144566 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:19947350..19947561 26863196 MeRIP-seq:(Medium) rs1267196513 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_784464,Human_RBP_ID_4757036,Human_RBP_ID_8943466,Human_RBP_ID_18805665,Human_RBP_ID_22092965 59983 RMVar_ID_59983 Human_SNP_ID_124969759 m1A Human chr3 + 19947390 19947390 19947390 GGCACGAGCCCCGCACAGTCCAGTGTGAGGGGAGCGGCGCTAAGAGCAGGCGACGCCGCCGCCGC GGCACGAGCCCCGCACAGTCCAGTGTGAGGGGCGCGGCGCTAAGAGCAGGCGACGCCGCCGCCGC A C RAB5A Ensembl:ENSG00000144566 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:19947350..19947561 26863196 MeRIP-seq:(Medium) rs888388891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784464,Human_RBP_ID_4757036,Human_RBP_ID_8943466,Human_RBP_ID_18805665,Human_RBP_ID_22092965 59984 RMVar_ID_59984 Human_SNP_ID_124995430 m1A Human chr3 - 20040392 20040390 20040393 CAGGGTCTCCCTCTCGGGCTCTGGTAGTCGGGAGAGCGAGACCCTCCCCCCACGCCCTCCCGCCC CAGGGTCTCCCTCTCGGGCTCTGGTAGTCGG___AGCGAGACCCTCCCCCCACGCCCTCCCGCCC TCTC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:20040390..20040573 26863196 MeRIP-seq:(Medium) rs1386473157 Functional Loss DEL dbSNP153 32..34 33 - - - 59985 RMVar_ID_59985 Human_SNP_ID_124995432 m1A Human chr3 - 20040392 20040392 20040392 CAGGGTCTCCCTCTCGGGCTCTGGTAGTCGGGAGAGCGAGACCCTCCCCCCACGCCCTCCCGCCC CAGGGTCTCCCTCTCGGGCTCTGGTAGTCGGGCGAGCGAGACCCTCCCCCCACGCCCTCCCGCCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:20040390..20040573 26863196 MeRIP-seq:(Medium) rs1472060426 Functional Loss SNV dbSNP153 33..33 33 - - - 59986 RMVar_ID_59986 Human_SNP_ID_124995534 m1A Human chr3 - 20040572 20040572 20040572 CGCAGGGGGAGCCCTGCGGGGGCGCGGGCGGAAGCGCCGCAGGCTGCGGGGGCAGCGCCCCGGGC CGCAGGGGGAGCCCTGCGGGGGCGCGGGCGGACGCGCCGCAGGCTGCGGGGGCAGCGCCCCGGGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr3:20040472..20040594;chr3:20040471..20040571 26863410 MeRIP-seq:(Medium) rs899390624 Functional Loss SNV dbSNP153 33..33 33 - - - 59987 RMVar_ID_59987 Human_SNP_ID_124995603 m1A Human chr3 + 20040720 20040720 20040720 GGCTCGGCCCGAATCGCCGTGAAGAAAGCGCAACTACGCTCCGCTCCGCGGGCCAAGAAACTGGA GGCTCGGCCCGAATCGCCGTGAAGAAAGCGCAGCTACGCTCCGCTCCGCGGGCCAAGAAACTGGA A G KAT2B Ensembl:ENSG00000114166 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:20040321..20095275 26863196 MeRIP-seq:(Medium) rs978866993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4737699 Human_Splice_Rec_401467,Human_Splice_Rec_401501 59988 RMVar_ID_59988 Human_SNP_ID_125009975 m1A Human chr3 + 20094611 20094611 20094611 GAGGAGAGAGTCAATGGACAGGTCACAAAACTATAGTAAGACAACAGAACAAAGATGCAAAAGTG GAGGAGAGAGTCAATGGACAGGTCACAAAACTGTAGTAAGACAACAGAACAAAGATGCAAAAGTG A G KAT2B Ensembl:ENSG00000114166 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:20094584..20094697 26863196 MeRIP-seq:(Medium) rs1361077077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59577,RMVar_hsa_circ_63489,RMVar_hsa_circ_72615 59989 RMVar_ID_59989 Human_SNP_ID_125668142 m1A Human chr3 + 22381760 22381760 22381760 ACATTGAGCTCCATAGAGACAGCGCCGGGGCAAGTGAGAGCCGGACGGGCACTGGGCGACTCTGT ACATTGAGCTCCATAGAGACAGCGCCGGGGCACGTGAGAGCCGGACGGGCACTGGGCGACTCTGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:22381701..22381800 26863196 MeRIP-seq:(Medium) rs551717800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_598953,Human_RBP_ID_4764305,Human_RBP_ID_9138626,Human_RBP_ID_14772353 59990 RMVar_ID_59990 Human_SNP_ID_125668144 m1A Human chr3 - 22381762 22381762 22381762 GCACAGAGTCGCCCAGTGCCCGTCCGGCTCTCACTTGCCCCGGCGCTGTCTCTATGGAGCTCAAT GCACAGAGTCGCCCAGTGCCCGTCCGGCTCTCGCTTGCCCCGGCGCTGTCTCTATGGAGCTCAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:22381722..22381812 26863196 MeRIP-seq:(Medium) rs1371739386 Functional Loss SNV dbSNP153 33..33 33 - - - 59991 RMVar_ID_59991 Human_SNP_ID_125899743 m1A Human chr3 - 23226551 23226551 23226551 TTCTTCAAAGCCAAGTTCACATCCCTCCTTAAAGATGTTTTCCTGGCCGGGCGCAGTGGCTCACA TTCTTCAAAGCCAAGTTCACATCCCTCCTTAAGGATGTTTTCCTGGCCGGGCGCAGTGGCTCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:23226545..23226658 26863196 MeRIP-seq:(Medium) rs1225099981 Functional Loss SNV dbSNP153 33..33 33 - - - 59992 RMVar_ID_59992 Human_SNP_ID_125929451 m1A Human chr3 + 23331375 23331375 23331375 CAAACAAAGAAAACAAAGTACTGCCAACCTGGAGTTTACATTGTAGTGGAGGAAGAAGAAAATGA CAAACAAAGAAAACAAAGTACTGCCAACCTGGCGTTTACATTGTAGTGGAGGAAGAAGAAAATGA A C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:23331367..23331794 26863196 MeRIP-seq:(Medium) rs1378522830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2776801,Human_RBP_ID_10090177 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 59993 RMVar_ID_59993 Human_SNP_ID_125999244 m1A Human chr3 - 23589840 23589840 23589840 TGTGCTTGCACAGGTCCCGCGGGGCGGCAGGCAGCAGGCCCCTATGTGGCGTACCGCTTGGTCCA TGTGCTTGCACAGGTCCCGCGGGGCGGCAGGCCGCAGGCCCCTATGTGGCGTACCGCTTGGTCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:23589793..23589869 26863196 MeRIP-seq:(Medium) rs772497815 Functional Loss SNV dbSNP153 33..33 33 - - - 59994 RMVar_ID_59994 Human_SNP_ID_125999258 m1A Human chr3 + 23589870 23589870 23589870 GCTGCCTGCCGCCCCGCGGGACCTGTGCAAGCACATTCACCAAGTGCATCGGTAGCCCTGCCCAC GCTGCCTGCCGCCCCGCGGGACCTGTGCAAGCGCATTCACCAAGTGCATCGGTAGCCCTGCCCAC A G UBE2E2 Ensembl:ENSG00000182247 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:23589799..23589975 26863196 MeRIP-seq:(Medium) rs752516965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7181456,Human_RBP_ID_17289777,Human_RBP_ID_17519447,Human_RBP_ID_26512007 Human_miRNA_ID_625681,Human_miRNA_ID_1332733,Human_miRNA_ID_2236169,Human_miRNA_ID_2478396 RMVar_hsa_circ_109322,RMVar_hsa_circ_216392 59995 RMVar_ID_59995 Human_SNP_ID_126055971 m1A Human chr3 - 23805965 23805965 23805965 AGAGAAGCGGAAGTGCAGCAACAGCAACTATTAAACAGGCAATGGCTTCCCCCAGCCACACACGC AGAGAAGCGGAAGTGCAGCAACAGCAACTATTGAACAGGCAATGGCTTCCCCCAGCCACACACGC T C UBE2E1-AS1 Ensembl:ENSG00000223791 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:23805914..23806086 26863196 MeRIP-seq:(Medium) rs1278951171 Functional Loss SNV dbSNP153 33..33 33 - - - 59996 RMVar_ID_59996 Human_SNP_ID_126059172 m1A Human chr3 - 23817644 23817644 23817644 CACTTCTCACCTCTTCCATGAAGCCTTCCCAGATCACTAAGTACTCCAGCCACAATCCCTCAAAC CACTTCTCACCTCTTCCATGAAGCCTTCCCAGTTCACTAAGTACTCCAGCCACAATCCCTCAAAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:23817637..23817803;chr3:23817639..23817748 26863196 MeRIP-seq:(Medium) rs1013300314 Functional Loss SNV dbSNP153 33..33 33 - - - 59997 RMVar_ID_59997 Human_SNP_ID_126059173 m1A Human chr3 - 23817644 23817644 23817644 CACTTCTCACCTCTTCCATGAAGCCTTCCCAGATCACTAAGTACTCCAGCCACAATCCCTCAAAC CACTTCTCACCTCTTCCATGAAGCCTTCCCAGGTCACTAAGTACTCCAGCCACAATCCCTCAAAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:23817637..23817803;chr3:23817639..23817748 26863196 MeRIP-seq:(Medium) rs1013300314 Functional Loss SNV dbSNP153 33..33 33 - - - 59998 RMVar_ID_59998 Human_SNP_ID_126086866 m1A Human chr3 + 23919226 23919226 23919226 AGGAGCGAGCTGGACGCCACTGTGGGGCTCTGAGAGTCCTGAATTCTTACTGGGTTGGTGAAGAT AGGAGCGAGCTGGACGCCACTGTGGGGCTCTGGGAGTCCTGAATTCTTACTGGGTTGGTGAAGAT A G RPL15 Ensembl:ENSG00000174748 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:23919176..23919275 32194978 MeRIP-seq:(Medium) rs3088096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248563,Human_RBP_ID_599131,Human_RBP_ID_785465,Human_RBP_ID_1032766,Human_RBP_ID_1205046,Human_RBP_ID_1625419,Human_RBP_ID_1960443,Human_RBP_ID_2777755,Human_RBP_ID_3703592,Human_RBP_ID_4757801,Human_RBP_ID_5209895,Human_RBP_ID_7182776,Human_RBP_ID_8569911,Human_RBP_ID_8871246,Human_RBP_ID_9138926,Human_RBP_ID_9334101,Human_RBP_ID_14779837,Human_RBP_ID_17289810,Human_RBP_ID_17403200,Human_RBP_ID_17519488,Human_RBP_ID_18003508,Human_RBP_ID_18337528,Human_RBP_ID_18806056,Human_RBP_ID_22279568,Human_RBP_ID_22456501,Human_RBP_ID_22509400,Human_RBP_ID_22823082,Human_RBP_ID_23022281,Human_RBP_ID_23135174,Human_RBP_ID_23213063,Human_RBP_ID_23995422,Human_RBP_ID_26512014,Human_RBP_ID_27050870,Human_RBP_ID_27159780,Human_RBP_ID_27316920,Human_RBP_ID_27500885,Human_RBP_ID_27566088,Human_RBP_ID_27717412 Human_Splice_Rec_402046,Human_Splice_Rec_402052,Human_Splice_Rec_402058,Human_Splice_Rec_402064,Human_Splice_Rec_402070,Human_Splice_Rec_402076,Human_Splice_Rec_402082,Human_Splice_Rec_402083,Human_Splice_Rec_402090,Human_Splice_Rec_402096,Human_Splice_Rec_402104,Human_Splice_Rec_402106,Human_Splice_Rec_402112,Human_Splice_Rec_402120,Human_Splice_Rec_402126,Human_Splice_Rec_402130 59999 RMVar_ID_59999 Human_SNP_ID_126086927 m1A Human chr3 - 23919425 23919425 23919425 CTGCCCGGCGAGAGCCACCAATAGTGTGGTGGAACTTGTGGCCCTTTCCAAGGCCACGGCTCTTT CTGCCCGGCGAGAGCCACCAATAGTGTGGTGGGACTTGTGGCCCTTTCCAAGGCCACGGCTCTTT T C NKIRAS1 Ensembl:ENSG00000197885 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:23919376..23919575 32194978 MeRIP-seq:(Medium) rs17851241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23995425 60000 RMVar_ID_60000 Human_SNP_ID_126086930 m1A Human chr3 + 23919431 23919431 23919431 CCGTGGCCTTGGAAAGGGCCACAAGTTCCACCACACTATTGGTGGCTCTCGCCGGGCAGCTTGGA CCGTGGCCTTGGAAAGGGCCACAAGTTCCACCGCACTATTGGTGGCTCTCGCCGGGCAGCTTGGA A G RPL15 Ensembl:ENSG00000174748 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:23919380..23919459 26863196 MeRIP-seq:(Medium) rs1456954396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_599136,Human_RBP_ID_1032767,Human_RBP_ID_1385550,Human_RBP_ID_1625424,Human_RBP_ID_1960445,Human_RBP_ID_3703593,Human_RBP_ID_8122867,Human_RBP_ID_8569913,Human_RBP_ID_9138927,Human_RBP_ID_17289811,Human_RBP_ID_17403201,Human_RBP_ID_17519490,Human_RBP_ID_17703738,Human_RBP_ID_18003510,Human_RBP_ID_18194505,Human_RBP_ID_22455734,Human_RBP_ID_27717413 60001 RMVar_ID_60001 Human_SNP_ID_126087045 m1A Human chr3 - 23919751 23919751 23919751 TTTTAAAGAATTTATTAAGCCTGTTATACCACACAGTATGTTTTATACACTGACATACAACTCCC TTTTAAAGAATTTATTAAGCCTGTTATACCACGCAGTATGTTTTATACACTGACATACAACTCCC T C NKIRAS1 Ensembl:ENSG00000197885 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:23919701..23919800 32194978 MeRIP-seq:(Medium) rs2360612 Functional Loss SNV dbSNP153 33..33 33 - - - 60002 RMVar_ID_60002 Human_SNP_ID_126193679 m1A Human chr3 - 24316370 24316370 24316370 CGAGGGAGAAGGGAAAAGAGAAAAAAGGAAGGAAAGGATGGAAAGAGGAGAGAAAAGAATATACC CGAGGGAGAAGGGAAAAGAGAAAAAAGGAAGGCAAGGATGGAAAGAGGAGAGAAAAGAATATACC T G THRB Ensembl:ENSG00000151090 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:24316350..24316473 26863196 MeRIP-seq:(Medium) rs566996769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10116758 RMVar_hsa_circ_58744,RMVar_hsa_circ_31108,RMVar_hsa_circ_45070,RMVar_hsa_circ_216415,RMVar_hsa_circ_293422,RMVar_hsa_circ_306875,RMVar_hsa_circ_283922,RMVar_hsa_circ_310057,RMVar_hsa_circ_312210,RMVar_hsa_circ_321343,RMVar_hsa_circ_216421,RMVar_hsa_circ_216416,RMVar_hsa_circ_216423,RMVar_hsa_circ_296980,RMVar_hsa_circ_216419,RMVar_hsa_circ_289736,RMVar_hsa_circ_216422,RMVar_hsa_circ_216420 60003 RMVar_ID_60003 Human_SNP_ID_126567752 m1A Human chr3 - 25645457 25645457 25645457 ATTTTTTGGTTAATTTTAGACTCTTTTTGATCAGAACAATGCTGCAAAAAAAGAAGAGTCAGAAA ATTTTTTGGTTAATTTTAGACTCTTTTTGATCGGAACAATGCTGCAAAAAAAGAAGAGTCAGAAA T C TOP2B Ensembl:ENSG00000077097 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:25645361..25645511 26863196 MeRIP-seq:(Medium) rs1423294607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4738412,Human_RBP_ID_25730139 Human_Splice_Rec_402614 RMVar_hsa_circ_78593,RMVar_hsa_circ_216435,RMVar_hsa_circ_40884,RMVar_hsa_circ_60513,RMVar_hsa_circ_299517,RMVar_hsa_circ_216466,RMVar_hsa_circ_50063,RMVar_hsa_circ_32001,RMVar_hsa_circ_53683,RMVar_hsa_circ_366060,RMVar_hsa_circ_346281,RMVar_hsa_circ_216474,RMVar_hsa_circ_282891,RMVar_hsa_circ_301123,RMVar_hsa_circ_216477 60004 RMVar_ID_60004 Human_SNP_ID_126572489 m1A Human chr3 + 25664279 25664279 25664279 GTTGCCGCCGCCCACGCCGGCTCCCGCGCCGCAGCCACCCGACTTGGCCATGGCGAGTGCCTCCA GTTGCCGCCGCCCACGCCGGCTCCCGCGCCGCGGCCACCCGACTTGGCCATGGCGAGTGCCTCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:25664261..25664439 26863410 MeRIP-seq:(Medium) rs1235525179 Functional Loss SNV dbSNP153 33..33 33 - - - 60005 RMVar_ID_60005 Human_SNP_ID_126572498 m1A Human chr3 + 25664296 25664296 25664296 CGGCTCCCGCGCCGCAGCCACCCGACTTGGCCATGGCGAGTGCCTCCAGCTCACAGGCCCTGAGG CGGCTCCCGCGCCGCAGCCACCCGACTTGGCCGTGGCGAGTGCCTCCAGCTCACAGGCCCTGAGG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:25664230..25664381 26863410 MeRIP-seq:(Medium) rs1246094875 Functional Loss SNV dbSNP153 33..33 33 - - - 60006 RMVar_ID_60006 Human_SNP_ID_126572536 m1A Human chr3 + 25664385 25664371 25664385 TGCGGGCCGCTGGGCCCCGCCGCTCCGCACCCACCGCTCCACTCGCCGCACTCCTAGCCGCGCCG TGCGGGCCGCTGGGCCCCG______________CCGCTCCACTCGCCGCACTCCTAGCCGCGCCG GCCGCTCCGCACCCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:25664199..25664925;chr3:25664226..25664925 26863196 MeRIP-seq:(Medium) rs1470757281 Functional Loss DEL dbSNP153 20..33 33 - - - 60007 RMVar_ID_60007 Human_SNP_ID_126602313 m1A Human chr3 - 25783390 25783390 25783390 GGGGCGGCGGCGGCGCCCGCTGGCGCTCAAGCATGGCGGCGGCGGCATTGGGCAGCTCCTCAGGC GGGGCGGCGGCGGCGCCCGCTGGCGCTCAAGCGTGGCGGCGGCGGCATTGGGCAGCTCCTCAGGC T C NGLY1 Ensembl:ENSG00000151092 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:25783301..25783425 26863410 MeRIP-seq:(Medium) rs772627507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757052,Human_RBP_ID_9334106,Human_RBP_ID_18424160 60008 RMVar_ID_60008 Human_SNP_ID_126602317 m1A Human chr3 - 25783394 25783394 25783394 GCGAGGGGCGGCGGCGGCGCCCGCTGGCGCTCAAGCATGGCGGCGGCGGCATTGGGCAGCTCCTC GCGAGGGGCGGCGGCGGCGCCCGCTGGCGCTCGAGCATGGCGGCGGCGGCATTGGGCAGCTCCTC T C NGLY1 Ensembl:ENSG00000151092 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:25783308..25783393 26863196 MeRIP-seq:(Medium) rs1007037983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757052,Human_RBP_ID_9334106,Human_RBP_ID_18424160 60009 RMVar_ID_60009 Human_SNP_ID_126602318 m1A Human chr3 - 25783394 25783394 25783394 GCGAGGGGCGGCGGCGGCGCCCGCTGGCGCTCAAGCATGGCGGCGGCGGCATTGGGCAGCTCCTC GCGAGGGGCGGCGGCGGCGCCCGCTGGCGCTCCAGCATGGCGGCGGCGGCATTGGGCAGCTCCTC T G NGLY1 Ensembl:ENSG00000151092 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:25783308..25783393 26863196 MeRIP-seq:(Medium) rs1007037983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757052,Human_RBP_ID_9334106,Human_RBP_ID_18424160 60010 RMVar_ID_60010 Human_SNP_ID_126602519 m1A Human chr3 - 25783700 25783700 25783700 CCCTGCCGGCCGAGGCCCCCCACCTTCTTCCGAACAGCCCCTTGCCCCCCGCGAAGGGGCAGCCG CCCTGCCGGCCGAGGCCCCCCACCTTCTTCCGGACAGCCCCTTGCCCCCCGCGAAGGGGCAGCCG T C NGLY1 Ensembl:ENSG00000151092 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:25783652..25783752 26863196 MeRIP-seq:(Medium) rs1291743800 Functional Loss SNV dbSNP153 33..33 33 - - - 60011 RMVar_ID_60011 Human_SNP_ID_127038444 m1A Human chr3 + 27407558 27407558 27407558 TCTCACATTCAGAAGTTTCCATTGTACCCATCAGAAGGCCTACCTACCCTTACCTTCCCCTCACA TCTCACATTCAGAAGTTTCCATTGTACCCATCGGAAGGCCTACCTACCCTTACCTTCCCCTCACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:27407508..27408022 26863196 MeRIP-seq:(Medium) rs543488847 Functional Loss SNV dbSNP153 33..33 33 - - - 60012 RMVar_ID_60012 Human_SNP_ID_127058759 m1A Human chr3 - 27484163 27484163 27484163 GCAGCGGCAGAAGCAGGCAGACCGCGCGGGGCAGTACCGTAGCGGCCGTCACGGGCTGGCCGGCC GCAGCGGCAGAAGCAGGCAGACCGCGCGGGGCGGTACCGTAGCGGCCGTCACGGGCTGGCCGGCC T C SLC4A7 Ensembl:ENSG00000033867 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:27484017..27484393 26863196 MeRIP-seq:(Medium) rs1002302588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756345 Human_Splice_Rec_403429,Human_Splice_Rec_403603,Human_Splice_Rec_403649,Human_Splice_Rec_403693,Human_Splice_Rec_403737,Human_Splice_Rec_403777,Human_Splice_Rec_403821,Human_Splice_Rec_403863,Human_Splice_Rec_403909,Human_Splice_Rec_403959,Human_Splice_Rec_404047 RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 60013 RMVar_ID_60013 Human_SNP_ID_127099621 m1A Human chr3 + 27633157 27633157 27633157 CCCTCAACCGACGCATCCAGCTCGTTGAGGAGAAGTTGGACAGGGCTCAGGAAAGACTGGCCACG CCCTCAACCGACGCATCCAGCTCGTTGAGGAGGAGTTGGACAGGGCTCAGGAAAGACTGGCCACG A G AC098614.2 Ensembl:ENSG00000271943 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1320428615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1859387 60014 RMVar_ID_60014 Human_SNP_ID_127099639 m1A Human chr3 + 27633236 27633236 27633236 GGAGGAGGCAGAAAAAGCTGCAGATGAGAGTGAGAGAGGAATGAAGGTGATAGAAAACCGGGCCA GGAGGAGGCAGAAAAAGCTGCAGATGAGAGTGTGAGAGGAATGAAGGTGATAGAAAACCGGGCCA A T AC098614.2 Ensembl:ENSG00000271943 Pseudogene exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:27633186..27633335 26863196 MeRIP-seq:(Medium) rs1228542732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_599644,Human_RBP_ID_1625672,Human_RBP_ID_3723908,Human_RBP_ID_5101916,Human_RBP_ID_7184837,Human_RBP_ID_8264756,Human_RBP_ID_18536338,Human_RBP_ID_23996552 Human_miRNA_ID_1839065 60015 RMVar_ID_60015 Human_SNP_ID_127250754 m1A Human chr3 - 28241690 28241690 28241690 GCTTGGGCTCGGACGCACGTGCGACCCCCGGGAGCTTCCCGCAACAGAAACACGGGCCCTTTGCA GCTTGGGCTCGGACGCACGTGCGACCCCCGGGGGCTTCCCGCAACAGAAACACGGGCCCTTTGCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:28241647..28241739 26863196 MeRIP-seq:(Medium) rs1426026010 Functional Loss SNV dbSNP153 33..33 33 - - - 60016 RMVar_ID_60016 Human_SNP_ID_127276553 m1A Human chr3 + 28348914 28348914 28348914 ATACGCGCGCGAGACCCAGGCCCGCCGTCGGGACCAGCACGGGCCGGAGGGAGGGGAAGCACTCC ATACGCGCGCGAGACCCAGGCCCGCCGTCGGGCCCAGCACGGGCCGGAGGGAGGGGAAGCACTCC A C ZCWPW2 Ensembl:ENSG00000206559 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:28348808..28349015 26863196 MeRIP-seq:(Medium) rs1004267192 Functional Loss SNV dbSNP153 33..33 33 - - - 60017 RMVar_ID_60017 Human_SNP_ID_103992068 m1A Human chr2 - 180005489 180005489 180005489 TCACTGCAAGCTCCGCCTCCCTAGTTCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAAGCTCCGCCTCCCTAGTTCATGCCGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C CWC22 Ensembl:ENSG00000163510 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:180005374..180005601 26863196 MeRIP-seq:(Medium) rs1368305783 Functional Loss SNV dbSNP153 33..33 33 - - - 60018 RMVar_ID_60018 Human_SNP_ID_104210296 m1A Human chr2 - 180873408 180873408 180873408 GCCGCCGCCTCTCCTTAGTCGCCGCAATGACGACCGCGTCCACCTCGCAGGTGCGCCAGAACTAC GCCGCCGCCTCTCCTTAGTCGCCGCAATGACGTCCGCGTCCACCTCGCAGGTGCGCCAGAACTAC T A FTH1P20 Ensembl:ENSG00000226564 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:180873358..180873461 26863196 MeRIP-seq:(Medium) rs374925004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17280295,Human_RBP_ID_17393674 60019 RMVar_ID_60019 Human_SNP_ID_104210307 m1A Human chr2 - 180873424 180873424 180873424 CGCAGCCACTGCCGCCGCCGCCGCCTCTCCTTAGTCGCCGCAATGACGACCGCGTCCACCTCGCA CGCAGCCACTGCCGCCGCCGCCGCCTCTCCTTGGTCGCCGCAATGACGACCGCGTCCACCTCGCA T C NONHSAG029990.2 RNACentral:URS00009BCDD6 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr2:180873376..180873467;chr2:180873392..180873500 26863410,26863196 MeRIP-seq:(Medium) rs1201638758 Functional Loss SNV dbSNP153 33..33 33 - - - 60020 RMVar_ID_60020 Human_SNP_ID_104235074 m1A Human chr2 - 180980677 180980677 180980677 GAGCTCCCGGCGAGGCGGAGGGGACGCGGGAGACCCCCGCGCGCTGTAGCCTCCCGCCGCCGCCG GAGCTCCCGGCGAGGCGGAGGGGACGCGGGAGGCCCCCGCGCGCTGTAGCCTCCCGCCGCCGCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:180980626..180980875 26863196 MeRIP-seq:(Medium) rs1334624625 Functional Loss SNV dbSNP153 33..33 33 - - - 60021 RMVar_ID_60021 Human_SNP_ID_104235075 m1A Human chr2 - 180980677 180980677 180980677 GAGCTCCCGGCGAGGCGGAGGGGACGCGGGAGACCCCCGCGCGCTGTAGCCTCCCGCCGCCGCCG GAGCTCCCGGCGAGGCGGAGGGGACGCGGGAGCCCCCCGCGCGCTGTAGCCTCCCGCCGCCGCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:180980626..180980875 26863196 MeRIP-seq:(Medium) rs1334624625 Functional Loss SNV dbSNP153 33..33 33 - - - 60022 RMVar_ID_60022 Human_SNP_ID_104235131 m1A Human chr2 + 180980790 180980790 180980790 TGGGCGGCGCCACCCTCCGGCCGGAGCCCGGCACTGCACAACCCCCTCCGACTTTCAATGTTCCA TGGGCGGCGCCACCCTCCGGCCGGAGCCCGGCGCTGCACAACCCCCTCCGACTTTCAATGTTCCA A G UBE2E3 Ensembl:ENSG00000170035 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:180980380..180981084;chr2:180980389..180981233 26863196 MeRIP-seq:(Medium) rs1386059347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539589,Human_RBP_ID_4623747,Human_RBP_ID_17274405 60023 RMVar_ID_60023 Human_SNP_ID_104235134 m1A Human chr2 + 180980795 180980795 180980795 GGCGCCACCCTCCGGCCGGAGCCCGGCACTGCACAACCCCCTCCGACTTTCAATGTTCCACACTC GGCGCCACCCTCCGGCCGGAGCCCGGCACTGCCCAACCCCCTCCGACTTTCAATGTTCCACACTC A C UBE2E3 Ensembl:ENSG00000170035 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr2:180980671..180981233;chr2:180980626..180981064 26863196 MeRIP-seq:(Medium) rs1482734344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539589,Human_RBP_ID_4623747,Human_RBP_ID_17274405,Human_RBP_ID_17945542 60024 RMVar_ID_60024 Human_SNP_ID_104235135 m1A Human chr2 + 180980795 180980795 180980795 GGCGCCACCCTCCGGCCGGAGCCCGGCACTGCACAACCCCCTCCGACTTTCAATGTTCCACACTC GGCGCCACCCTCCGGCCGGAGCCCGGCACTGCGCAACCCCCTCCGACTTTCAATGTTCCACACTC A G UBE2E3 Ensembl:ENSG00000170035 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr2:180980671..180981233;chr2:180980626..180981064 26863196 MeRIP-seq:(Medium) rs1482734344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539589,Human_RBP_ID_4623747,Human_RBP_ID_17274405,Human_RBP_ID_17945542 60025 RMVar_ID_60025 Human_SNP_ID_104235518 m1A Human chr2 - 180981958 180981958 180981958 GAGAAAATGTTAAATCTAGGAAATAAACCAACAGCATTTTCTTCTAGTCATCTAAAATCGTCTTG GAGAAAATGTTAAATCTAGGAAATAAACCAACTGCATTTTCTTCTAGTCATCTAAAATCGTCTTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:180981956..180982039 26863196 MeRIP-seq:(Medium) rs1010858815 Functional Loss SNV dbSNP153 33..33 33 - - - 60026 RMVar_ID_60026 Human_SNP_ID_104235523 m1A Human chr2 - 180981970 180981970 180981970 GGGGAGGAGGAGGAGAAAATGTTAAATCTAGGAAATAAACCAACAGCATTTTCTTCTAGTCATCT GGGGAGGAGGAGGAGAAAATGTTAAATCTAGGCAATAAACCAACAGCATTTTCTTCTAGTCATCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:180981968..180982041 26863196 MeRIP-seq:(Medium) rs1022205875 Functional Loss SNV dbSNP153 33..33 33 - - - 60027 RMVar_ID_60027 Human_SNP_ID_104461214 m1A Human chr2 + 181892058 181892058 181892058 GCGCAGGGTCCGGCTGGGGTAGCGGAGCCCCCAGTGCGGCCATGGACCGGCCCCTGTCGTCGTCG GCGCAGGGTCCGGCTGGGGTAGCGGAGCCCCCCGTGCGGCCATGGACCGGCCCCTGTCGTCGTCG A C ITPRID2 Ensembl:ENSG00000138434 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:181891973..181892148 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4622780,Human_RBP_ID_5240008,Human_RBP_ID_18421955,Human_RBP_ID_22450619,Human_RBP_ID_27817824 RMVar_hsa_circ_204970,RMVar_hsa_circ_97429,RMVar_hsa_circ_107766,RMVar_hsa_circ_204971 60028 RMVar_ID_60028 Human_SNP_ID_104461215 m1A Human chr2 + 181892058 181892058 181892058 GCGCAGGGTCCGGCTGGGGTAGCGGAGCCCCCAGTGCGGCCATGGACCGGCCCCTGTCGTCGTCG GCGCAGGGTCCGGCTGGGGTAGCGGAGCCCCCTGTGCGGCCATGGACCGGCCCCTGTCGTCGTCG A T ITPRID2 Ensembl:ENSG00000138434 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:181891973..181892148 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4622780,Human_RBP_ID_5240008,Human_RBP_ID_18421955,Human_RBP_ID_22450619,Human_RBP_ID_27817824 RMVar_hsa_circ_204970,RMVar_hsa_circ_97429,RMVar_hsa_circ_107766,RMVar_hsa_circ_204971 60029 RMVar_ID_60029 Human_SNP_ID_104461299 m1A Human chr2 + 181892227 181892222 181892228 CACAGAAGCGACGACGCAGGACGAGGAGGAGGACGAGGAGGAGGACCTCCCCGGCGCGCAGCTGC CACAGAAGCGACGACGCAGGACGAGGAG______GAGGAGGAGGACCTCCCCGGCGCGCAGCTGC GGAGGAC G ITPRID2 Ensembl:ENSG00000138434 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:181891882..181892675 26863196 MeRIP-seq:(Medium) rs1377424955 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_242879,Human_RBP_ID_828938,Human_RBP_ID_920949,Human_RBP_ID_9385139,Human_RBP_ID_18470868,Human_RBP_ID_19002704,Human_RBP_ID_22996898,Human_RBP_ID_26340137,Human_RBP_ID_27476248 Human_Splice_Rec_333871,Human_Splice_Rec_333905,Human_Splice_Rec_333907,Human_Splice_Rec_333939,Human_Splice_Rec_333971,Human_Splice_Rec_334001 RMVar_hsa_circ_204970,RMVar_hsa_circ_97429,RMVar_hsa_circ_107766,RMVar_hsa_circ_204971 60030 RMVar_ID_60030 Human_SNP_ID_104461301 m1A Human chr2 + 181892227 181892227 181892227 CACAGAAGCGACGACGCAGGACGAGGAGGAGGACGAGGAGGAGGACCTCCCCGGCGCGCAGCTGC CACAGAAGCGACGACGCAGGACGAGGAGGAGGTCGAGGAGGAGGACCTCCCCGGCGCGCAGCTGC A T ITPRID2 Ensembl:ENSG00000138434 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:181891882..181892675 26863196 MeRIP-seq:(Medium) rs1448660670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242879,Human_RBP_ID_828938,Human_RBP_ID_920949,Human_RBP_ID_9385139,Human_RBP_ID_18470868,Human_RBP_ID_19002704,Human_RBP_ID_22996898,Human_RBP_ID_26340137,Human_RBP_ID_27476248 Human_Splice_Rec_333871,Human_Splice_Rec_333905,Human_Splice_Rec_333907,Human_Splice_Rec_333939,Human_Splice_Rec_333971,Human_Splice_Rec_334001 RMVar_hsa_circ_204970,RMVar_hsa_circ_97429,RMVar_hsa_circ_107766,RMVar_hsa_circ_204971 60031 RMVar_ID_60031 Human_SNP_ID_104461315 m1A Human chr2 - 181892257 181892257 181892257 GGGAGCACCGACCTCTTCCCCCCGCTGCCGGCAGCTGCGCGCCGGGGAGGTCCTCCTCCTCGTCC GGGAGCACCGACCTCTTCCCCCCGCTGCCGGCGGCTGCGCGCCGGGGAGGTCCTCCTCCTCGTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:181891926..181892309;chr2:181891926..181892701;chr2:181891926..181892725 26863196 MeRIP-seq:(Medium) rs1215568700 Functional Loss SNV dbSNP153 33..33 33 - - - 60032 RMVar_ID_60032 Human_SNP_ID_104735676 m1A Human chr2 - 183013794 183013794 183013794 CAGAGTAGATGATTGAAGGGGACGGTGGTAGGACATGAAGTGCCAGTGGTTGTAATGAATAGGCA CAGAGTAGATGATTGAAGGGGACGGTGGTAGGGCATGAAGTGCCAGTGGTTGTAATGAATAGGCA T C NCKAP1 Ensembl:ENSG00000061676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:183013793..183013947 26863196 MeRIP-seq:(Medium) rs995592160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34471,RMVar_hsa_circ_351246,RMVar_hsa_circ_26770,RMVar_hsa_circ_205011,RMVar_hsa_circ_315456,RMVar_hsa_circ_205020,RMVar_hsa_circ_78903,RMVar_hsa_circ_81568,RMVar_hsa_circ_205042,RMVar_hsa_circ_205043,RMVar_hsa_circ_312941,RMVar_hsa_circ_276200,RMVar_hsa_circ_205054,RMVar_hsa_circ_30911,RMVar_hsa_circ_103188,RMVar_hsa_circ_205057,RMVar_hsa_circ_43169,RMVar_hsa_circ_323288,RMVar_hsa_circ_205064,RMVar_hsa_circ_275950,RMVar_hsa_circ_205066,RMVar_hsa_circ_205067,RMVar_hsa_circ_46344 60033 RMVar_ID_60033 Human_SNP_ID_104738048 m1A Human chr2 - 183023918 183023918 183023918 CATTTCACTTTTTTTTATTACTGTTGTTTTATAGGCATGTGGAGACCCCAAGGCAAAACCATCCT CATTTCACTTTTTTTTATTACTGTTGTTTTATTGGCATGTGGAGACCCCAAGGCAAAACCATCCT T A NCKAP1 Ensembl:ENSG00000061676 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr2:183023876..183023925;chr2:183023876..183023987 26863196,32194978 MeRIP-seq:(Medium) rs775973136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4628801,Human_RBP_ID_6861557,Human_RBP_ID_13708727,Human_RBP_ID_18422779,Human_RBP_ID_25576895 RMVar_hsa_circ_78903,RMVar_hsa_circ_205043,RMVar_hsa_circ_103188,RMVar_hsa_circ_205066 60034 RMVar_ID_60034 Human_SNP_ID_104741627 m1A Human chr2 - 183038326 183038326 183038326 GGGTGGGGGCGGAAGGGCGGCGGGCGGAAGGCAGGAGGCTGCCGGGGCGCGGGCTGCTGCGGGAG GGGTGGGGGCGGAAGGGCGGCGGGCGGAAGGCCGGAGGCTGCCGGGGCGCGGGCTGCTGCGGGAG T G NCKAP1 Ensembl:ENSG00000061676 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:183037981..183038500;chr2:183023851..183038464;chr2:183037976..183038468;chr2:183037976..183038446 26863196 MeRIP-seq:(Medium) rs1198128858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264268,Human_RBP_ID_774530,Human_RBP_ID_827429,Human_RBP_ID_3638235,Human_RBP_ID_3958407,Human_RBP_ID_4622788,Human_RBP_ID_5146926,Human_RBP_ID_5322244,Human_RBP_ID_8200751,Human_RBP_ID_8234023,Human_RBP_ID_8728560,Human_RBP_ID_9330748,Human_RBP_ID_9353821,Human_RBP_ID_9428880,Human_RBP_ID_17068687,Human_RBP_ID_18422705,Human_RBP_ID_18948421,Human_RBP_ID_26786357,Human_RBP_ID_27817846 RMVar_hsa_circ_78903,RMVar_hsa_circ_205043 60035 RMVar_ID_60035 Human_SNP_ID_104766126 m1A Human chr2 - 183134507 183134503 183134507 AAACTTCCGACCTCCAGAAATGAAAGATAATGAATGTGTATTGTTTAAGCCACTTTTATGTTTGT AAACTTCCGACCTCCAGAAATGAAAGATAATG____TGTATTGTTTAAGCCACTTTTATGTTTGT ACATT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:183134471..183134598 26863196 MeRIP-seq:(Medium) rs1231075228 Functional Loss DEL dbSNP153 33..36 33 - - - 60036 RMVar_ID_60036 Human_SNP_ID_104885650 m1A Human chr2 - 183607609 183607609 183607609 ACAAGGTGGGATTACCTGACCCAGGTTGAAAAAGAGTGCAAAGAAAAAGAGAAGCCCTCCTATGA ACAAGGTGGGATTACCTGACCCAGGTTGAAAAGGAGTGCAAAGAAAAAGAGAAGCCCTCCTATGA T C CACYBPP2 Ensembl:ENSG00000177855 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878959244 Functional Loss SNV dbSNP153 33..33 33 - - - 60037 RMVar_ID_60037 Human_SNP_ID_105133800 m1A Human chr2 - 184598954 184598954 184598954 GCTGATGACAATGTAGTAACACTCCATGGGGCAGCCGCCGCCTCCTCCGCCGCAGCCGCCGCTTC GCTGATGACAATGTAGTAACACTCCATGGGGCGGCCGCCGCCTCCTCCGCCGCAGCCGCCGCTTC T C AC096667.1 Ensembl:ENSG00000283839 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:184598908..184599008 32194978 MeRIP-seq:(Medium) rs749172695 Functional Loss SNV dbSNP153 33..33 33 - - - 60038 RMVar_ID_60038 Human_SNP_ID_105524391 m1A Human chr2 - 186150249 186150249 186150249 AGAGGTCAGGTAGAAAAGGAATCAAGAAAGGAAACAAAAGCAGCAGGCAGTGATGAGGAGAAAAC AGAGGTCAGGTAGAAAAGGAATCAAGAAAGGAGACAAAAGCAGCAGGCAGTGATGAGGAGAAAAC T C LINC01473 Ensembl:ENSG00000237877 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:186150199..186150293 26863196 MeRIP-seq:(Medium) rs1277462045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2608895 60039 RMVar_ID_60039 Human_SNP_ID_105612471 m1A Human chr2 + 186502577 186502577 186502577 GAAGCACGGTGAGGCGGAAAAGAAAAAACCAAAAACTCAAATAGTATGTCCTTTTCTTGAATTGA GAAGCACGGTGAGGCGGAAAAGAAAAAACCAAGAACTCAAATAGTATGTCCTTTTCTTGAATTGA A G ZC3H15 Ensembl:ENSG00000065548 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:186502526..186502600 32194978 MeRIP-seq:(Medium) rs1411937545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774533,Human_RBP_ID_1592372,Human_RBP_ID_26340153,Human_RBP_ID_27819209 Human_Splice_Rec_335438,Human_Splice_Rec_335439,Human_Splice_Rec_335474,Human_Splice_Rec_335484 RMVar_hsa_circ_82811,RMVar_hsa_circ_205104,RMVar_hsa_circ_360736,RMVar_hsa_circ_98901,RMVar_hsa_circ_124649,RMVar_hsa_circ_205106,RMVar_hsa_circ_361443,RMVar_hsa_circ_56792,RMVar_hsa_circ_205107 60040 RMVar_ID_60040 Human_SNP_ID_105632944 m1A Human chr2 - 186590278 186590278 186590278 GGGAGCGGTAGCCACCTCCCCCCGCCCCAGCGAGGCGCCCAGTGCCCGCGGCCCGCCGCCTGCGC GGGAGCGGTAGCCACCTCCCCCCGCCCCAGCGCGGCGCCCAGTGCCCGCGGCCCGCCGCCTGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:186590229..186590404 26863196 MeRIP-seq:(Medium) rs1013738573 Functional Loss SNV dbSNP153 33..33 33 - - - 60041 RMVar_ID_60041 Human_SNP_ID_105645172 m1A Human chr2 - 186641530 186641530 186641530 CCCAAAGGAGCTATGGCACTGCCAAACCGTGCAAAGACCTCAAATCCATTCAGCTTTGTCGTCTG CCCAAAGGAGCTATGGCACTGCCAAACCGTGCGAAGACCTCAAATCCATTCAGCTTTGTCGTCTG T C AC017101.1 Ensembl:ENSG00000227227 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:186641433..186641576 32194978 MeRIP-seq:(Medium) rs201824820 Functional Loss SNV dbSNP153 33..33 33 - - - 60042 RMVar_ID_60042 Human_SNP_ID_106036880 m1A Human chr2 - 188292508 188292506 188292508 TTCCTGCTCACCGGCCCCCCGCCGCCGGACCAAAGTTACCACAAAAGGCTAAGGAGGTTTCTGGA TTCCTGCTCACCGGCCCCCCGCCGCCGGACCA__GTTACCACAAAAGGCTAAGGAGGTTTCTGGA CTT C LINC01090 Ensembl:ENSG00000231689 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188292497..188292672 26863196 MeRIP-seq:(Medium) rs748699468 Functional Loss DEL dbSNP153 33..34 33 - - - 60043 RMVar_ID_60043 Human_SNP_ID_106036881 m1A Human chr2 - 188292508 188292508 188292508 TTCCTGCTCACCGGCCCCCCGCCGCCGGACCAAAGTTACCACAAAAGGCTAAGGAGGTTTCTGGA TTCCTGCTCACCGGCCCCCCGCCGCCGGACCACAGTTACCACAAAAGGCTAAGGAGGTTTCTGGA T G LINC01090 Ensembl:ENSG00000231689 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188292497..188292672 26863196 MeRIP-seq:(Medium) rs1268375613 Functional Loss SNV dbSNP153 33..33 33 - - - 60044 RMVar_ID_60044 Human_SNP_ID_106106622 m1A Human chr2 - 188594045 188594045 188594045 AATAATAATAAATGACATGTGTATACAAACACATTTAACATGAATCAGGATTTCTTGTTCTTGAT AATAATAATAAATGACATGTGTATACAAACACCTTTAACATGAATCAGGATTTCTTGTTCTTGAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:188594003..188594092 32194978 MeRIP-seq:(Medium) rs199874668 Functional Loss SNV dbSNP153 33..33 33 - - - 60045 RMVar_ID_60045 Human_SNP_ID_106199944 m1A Human chr2 + 188985247 188985247 188985247 GGTCAAGGACCTCAAGGCCCCAAGGGAGATCCAGTAAGTAAACATTCTTCAGTAGAATAAAATTA GGTCAAGGACCTCAAGGCCCCAAGGGAGATCCGGTAAGTAAACATTCTTCAGTAGAATAAAATTA A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:188985176..188985250 32194978 MeRIP-seq:(Medium) rs1394127532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336268,Human_Splice_Rec_336269,Human_Splice_Rec_336368,Human_Splice_Rec_336369 RMVar_hsa_circ_100088,RMVar_hsa_circ_111421,RMVar_hsa_circ_109620,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205165,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_205166,RMVar_hsa_circ_96427,RMVar_hsa_circ_86433,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_205170,RMVar_hsa_circ_124939,RMVar_hsa_circ_108688,RMVar_hsa_circ_115502,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_43135,RMVar_hsa_circ_87403,RMVar_hsa_circ_205176,RMVar_hsa_circ_205178,RMVar_hsa_circ_205179,RMVar_hsa_circ_205177,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173 60046 RMVar_ID_60046 Human_SNP_ID_106200061 m1A Human chr2 - 188985678 188985678 188985678 CTGGAATACCAGGGTCACCATTTCTCCCAGGAATACCAGGAGGGCCCTAAAAAAGAGATAAAAAT CTGGAATACCAGGGTCACCATTTCTCCCAGGACTACCAGGAGGGCCCTAAAAAAGAGATAAAAAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:188985673..188988093 32194978 MeRIP-seq:(Medium) rs769622439 Functional Loss SNV dbSNP153 33..33 33 - - - 60047 RMVar_ID_60047 Human_SNP_ID_106201825 m1A Human chr2 - 188992195 188992195 188992195 GGTTGACCATCACTGCCTCGAGCACCGTCATTACCCCGAGCACCCTAAAAAGAGAAGTTTACATC GGTTGACCATCACTGCCTCGAGCACCGTCATTTCCCCGAGCACCCTAAAAAGAGAAGTTTACATC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:188992176..188992250 26863196 MeRIP-seq:(Medium) rs771292385 Functional Loss SNV dbSNP153 33..33 33 - - - 60048 RMVar_ID_60048 Human_SNP_ID_106201826 m1A Human chr2 - 188992195 188992195 188992195 GGTTGACCATCACTGCCTCGAGCACCGTCATTACCCCGAGCACCCTAAAAAGAGAAGTTTACATC GGTTGACCATCACTGCCTCGAGCACCGTCATTGCCCCGAGCACCCTAAAAAGAGAAGTTTACATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:188992176..188992250 26863196 MeRIP-seq:(Medium) rs771292385 Functional Loss SNV dbSNP153 33..33 33 - - - 60049 RMVar_ID_60049 Human_SNP_ID_106201999 m1A Human chr2 - 188992878 188992878 188992878 AGTTCCAGGAGGACCAGGAGGGCCCTGAAAAAATTAAATACAATTTCAAGAGCTCTTTTTCAACT AGTTCCAGGAGGACCAGGAGGGCCCTGAAAAATTTAAATACAATTTCAAGAGCTCTTTTTCAACT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188992876..188992900 26863196 MeRIP-seq:(Medium) rs1278617595 Functional Loss SNV dbSNP153 33..33 33 - - - 60050 RMVar_ID_60050 Human_SNP_ID_106202392 m1A Human chr2 - 188994284 188994284 188994284 CCAGGAGCACCATTAGCACCGGCTGGTCCTGGAGGACCCCGGGCTCCCATCAGTCCAGGAGCTCC CCAGGAGCACCATTAGCACCGGCTGGTCCTGGGGGACCCCGGGCTCCCATCAGTCCAGGAGCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188994193..188994371 26863196 MeRIP-seq:(Medium) rs772726982 Functional Loss SNV dbSNP153 33..33 33 - - - 60051 RMVar_ID_60051 Human_SNP_ID_106202416 m1A Human chr2 - 188994326 188994326 188994326 AACAGAGAAAAAACAAGGCAACTTACTGCACCACCTCGCAGTCCAGGAGCACCATTAGCACCGGC AACAGAGAAAAAACAAGGCAACTTACTGCACCGCCTCGCAGTCCAGGAGCACCATTAGCACCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188994226..188994361 26863196 MeRIP-seq:(Medium) rs1289997955 Functional Loss SNV dbSNP153 33..33 33 - - - 60052 RMVar_ID_60052 Human_SNP_ID_106202592 m1A Human chr2 + 188994829 188994829 188994829 GTGCAAATGGGCTTCCAGGAGCTGCAGGAGAAAGGGTACGTTTTCCATGGGGCATCTAAAAGAAA GTGCAAATGGGCTTCCAGGAGCTGCAGGAGAAGGGGTACGTTTTCCATGGGGCATCTAAAAGAAA A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188994701..188994850 26863196 MeRIP-seq:(Medium) rs771070731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336303,Human_Splice_Rec_336403 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_125194,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205191,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_97783,RMVar_hsa_circ_205194,RMVar_hsa_circ_205198,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_91322,RMVar_hsa_circ_205206,RMVar_hsa_circ_78566,RMVar_hsa_circ_32244,RMVar_hsa_circ_65714,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_67768,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_362709 60053 RMVar_ID_60053 Human_SNP_ID_106202875 m1A Human chr2 + 188995788 188995788 188995788 GCAGAGATGGCGTCCCTGGAGGTCCAGGAATGAGGGTACAGAGAAACATTTGTTTGAATGACACT GCAGAGATGGCGTCCCTGGAGGTCCAGGAATGGGGGTACAGAGAAACATTTGTTTGAATGACACT A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188995640..188995839 26863196 MeRIP-seq:(Medium) rs1251091868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336306,Human_Splice_Rec_336307,Human_Splice_Rec_336406,Human_Splice_Rec_336407 RMVar_hsa_circ_14000,RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_125194,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205191,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_97783,RMVar_hsa_circ_205194,RMVar_hsa_circ_205198,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_91322,RMVar_hsa_circ_205206,RMVar_hsa_circ_78566,RMVar_hsa_circ_32244,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_67768,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_365153,RMVar_hsa_circ_89524,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216 60054 RMVar_ID_60054 Human_SNP_ID_106203160 m1A Human chr2 - 188996379 188996379 188996379 TCTCCTTGACTTCCCTAATAAGAAAAAATTACATTAATAAAGGTTTGATAAAGAGAAGATTAAAG TCTCCTTGACTTCCCTAATAAGAAAAAATTACTTTAATAAAGGTTTGATAAAGAGAAGATTAAAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188996376..188996500 26863196 MeRIP-seq:(Medium) rs367750985 Functional Loss SNV dbSNP153 33..33 33 - - - 60055 RMVar_ID_60055 Human_SNP_ID_106203161 m1A Human chr2 - 188996379 188996379 188996379 TCTCCTTGACTTCCCTAATAAGAAAAAATTACATTAATAAAGGTTTGATAAAGAGAAGATTAAAG TCTCCTTGACTTCCCTAATAAGAAAAAATTACGTTAATAAAGGTTTGATAAAGAGAAGATTAAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188996376..188996500 26863196 MeRIP-seq:(Medium) rs367750985 Functional Loss SNV dbSNP153 33..33 33 - - - 60056 RMVar_ID_60056 Human_SNP_ID_106203162 m1A Human chr2 - 188996379 188996379 188996379 TCTCCTTGACTTCCCTAATAAGAAAAAATTACATTAATAAAGGTTTGATAAAGAGAAGATTAAAG TCTCCTTGACTTCCCTAATAAGAAAAAATTACCTTAATAAAGGTTTGATAAAGAGAAGATTAAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188996376..188996500 26863196 MeRIP-seq:(Medium) rs367750985 Functional Loss SNV dbSNP153 33..33 33 - - - 60057 RMVar_ID_60057 Human_SNP_ID_106203440 m1A Human chr2 + 188997236 188997236 188997236 GGACCTGGCCCTCAGGTACGTAGCTTTCCTCAATTTATTTCTAGCCTTCTAATAGATGCGTTCAT GGACCTGGCCCTCAGGTACGTAGCTTTCCTCAGTTTATTTCTAGCCTTCTAATAGATGCGTTCAT A G COL3A1 Ensembl:ENSG00000168542 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188997234..188997321 26863196 MeRIP-seq:(Medium) rs28413125 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_336312,Human_Splice_Rec_336412 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_56534,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_79379,RMVar_hsa_circ_205218 60058 RMVar_ID_60058 Human_SNP_ID_106203489 m1A Human chr2 + 188997380 188997380 188997380 AAGAATGGTGAAACTGGACCTCAGGGACCCCCAGGGCCTACTGTAAGTTCACTCATATAAAATTG AAGAATGGTGAAACTGGACCTCAGGGACCCCCTGGGCCTACTGTAAGTTCACTCATATAAAATTG A T COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188997151..188997400 26863196 MeRIP-seq:(Medium) rs141128796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336314,Human_Splice_Rec_336315,Human_Splice_Rec_336414,Human_Splice_Rec_336415 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_56534,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_79379,RMVar_hsa_circ_205218,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220 60059 RMVar_ID_60059 Human_SNP_ID_106203599 m1A Human chr2 + 188997720 188997720 188997720 ATACTTTTCTAGGGGCCTGGTGGTGACAAAGGAGACACAGGACCCCCTGGTCCACAAGGATTACA ATACTTTTCTAGGGGCCTGGTGGTGACAAAGGTGACACAGGACCCCCTGGTCCACAAGGATTACA A T COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:188997701..188997775 26863196 MeRIP-seq:(Medium) rs1397481099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336316,Human_Splice_Rec_336317,Human_Splice_Rec_336416,Human_Splice_Rec_336417 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_105049,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205193,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_56534,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_79379,RMVar_hsa_circ_205218,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221 60060 RMVar_ID_60060 Human_SNP_ID_106204078 m1A Human chr2 + 188999377 188999377 188999377 AGAGGTGGAGCTGGTCCCCCTGGTCCCGAAGGAGGAAAGGTAACTCCACAGCATTCCATTCACCT AGAGGTGGAGCTGGTCCCCCTGGTCCCGAAGGCGGAAAGGTAACTCCACAGCATTCCATTCACCT A C COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:188999326..188999400 26863196 MeRIP-seq:(Medium) rs1166127350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336322,Human_Splice_Rec_336323,Human_Splice_Rec_336422,Human_Splice_Rec_336423 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_205196,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_56534,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_286207,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_358421,RMVar_hsa_circ_353094,RMVar_hsa_circ_99747,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205224,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225 60061 RMVar_ID_60061 Human_SNP_ID_106204156 m1A Human chr2 + 188999575 188999575 188999575 GAGGTCTTGGAAGTCCTGGTCCAAAGGGTGACAAGGTGTTGACTTGTTTTCTCTTAATTGTTCAA GAGGTCTTGGAAGTCCTGGTCCAAAGGGTGACGAGGTGTTGACTTGTTTTCTCTTAATTGTTCAA A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:188999476..188999600 26863196 MeRIP-seq:(Medium) rs754331056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336325,Human_Splice_Rec_336425 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_358421,RMVar_hsa_circ_353094,RMVar_hsa_circ_99747,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205224,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_27739,RMVar_hsa_circ_66658,RMVar_hsa_circ_205229 60062 RMVar_ID_60062 Human_SNP_ID_106204157 m1A Human chr2 + 188999576 188999576 188999576 AGGTCTTGGAAGTCCTGGTCCAAAGGGTGACAAGGTGTTGACTTGTTTTCTCTTAATTGTTCAAT AGGTCTTGGAAGTCCTGGTCCAAAGGGTGACACGGTGTTGACTTGTTTTCTCTTAATTGTTCAAT A C COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:188999451..188999575;chr2:188999526..188999600;chr2:188999551..188999600 26863196 MeRIP-seq:(Medium) rs1307941220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336325,Human_Splice_Rec_336425 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_358421,RMVar_hsa_circ_353094,RMVar_hsa_circ_99747,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205224,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_27739,RMVar_hsa_circ_66658,RMVar_hsa_circ_205229 60063 RMVar_ID_60063 Human_SNP_ID_106204632 m1A Human chr2 - 189001447 189001447 189001447 TTTTATATCCAGGTAGTATTAAGGGTTACCTTATCTCCAGGCTGGCCAGCTGGGCCAGGAGGACC TTTTATATCCAGGTAGTATTAAGGGTTACCTTCTCTCCAGGCTGGCCAGCTGGGCCAGGAGGACC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:189001376..189001475 26863196 MeRIP-seq:(Medium) rs1369704939 Functional Loss SNV dbSNP153 33..33 33 - - - 60064 RMVar_ID_60064 Human_SNP_ID_106204677 m1A Human chr2 + 189001556 189001556 189001556 CTCTTTTTCCAGGGTGAAGGTGGTGCCCCCGGACTTCCAGGTATAGCTGGACCTCGTGGTAGCCC CTCTTTTTCCAGGGTGAAGGTGGTGCCCCCGGGCTTCCAGGTATAGCTGGACCTCGTGGTAGCCC A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:189001526..189001575 26863196 MeRIP-seq:(Medium) rs1207914999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336330,Human_Splice_Rec_336331,Human_Splice_Rec_336430,Human_Splice_Rec_336431 Human_miRNA_ID_2362528 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_78566,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_66984,RMVar_hsa_circ_82223,RMVar_hsa_circ_205233,RMVar_hsa_circ_268303,RMVar_hsa_circ_80204,RMVar_hsa_circ_205234,RMVar_hsa_circ_205235 60065 RMVar_ID_60065 Human_SNP_ID_106204679 m1A Human chr2 + 189001562 189001562 189001562 TTCCAGGGTGAAGGTGGTGCCCCCGGACTTCCAGGTATAGCTGGACCTCGTGGTAGCCCTGTAAG TTCCAGGGTGAAGGTGGTGCCCCCGGACTTCCCGGTATAGCTGGACCTCGTGGTAGCCCTGTAAG A C COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:189001526..189001600 26863196 MeRIP-seq:(Medium) rs886055332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336330,Human_Splice_Rec_336331,Human_Splice_Rec_336430,Human_Splice_Rec_336431 Human_miRNA_ID_2362528 Clinvar_Rec_202 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_78566,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_66984,RMVar_hsa_circ_82223,RMVar_hsa_circ_205233,RMVar_hsa_circ_268303,RMVar_hsa_circ_80204,RMVar_hsa_circ_205234,RMVar_hsa_circ_205235 60066 RMVar_ID_60066 Human_SNP_ID_106204680 m1A Human chr2 + 189001562 189001562 189001562 TTCCAGGGTGAAGGTGGTGCCCCCGGACTTCCAGGTATAGCTGGACCTCGTGGTAGCCCTGTAAG TTCCAGGGTGAAGGTGGTGCCCCCGGACTTCCGGGTATAGCTGGACCTCGTGGTAGCCCTGTAAG A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:189001526..189001600 26863196 MeRIP-seq:(Medium) rs886055332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336330,Human_Splice_Rec_336331,Human_Splice_Rec_336430,Human_Splice_Rec_336431 Human_miRNA_ID_2362528 Clinvar_Rec_202 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_78566,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_66984,RMVar_hsa_circ_82223,RMVar_hsa_circ_205233,RMVar_hsa_circ_268303,RMVar_hsa_circ_80204,RMVar_hsa_circ_205234,RMVar_hsa_circ_205235 60067 RMVar_ID_60067 Human_SNP_ID_106204684 m1A Human chr2 - 189001571 189001571 189001571 TCTTTAACACTTACAGGGCTACCACGAGGTCCAGCTATACCTGGAAGTCCGGGGGCACCACCTTC TCTTTAACACTTACAGGGCTACCACGAGGTCCGGCTATACCTGGAAGTCCGGGGGCACCACCTTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:189001376..189001600 26863196 MeRIP-seq:(Medium) rs200452382 Functional Loss SNV dbSNP153 33..33 33 - - - 60068 RMVar_ID_60068 Human_SNP_ID_106204685 m1A Human chr2 - 189001571 189001571 189001571 TCTTTAACACTTACAGGGCTACCACGAGGTCCAGCTATACCTGGAAGTCCGGGGGCACCACCTTC TCTTTAACACTTACAGGGCTACCACGAGGTCCCGCTATACCTGGAAGTCCGGGGGCACCACCTTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:189001376..189001600 26863196 MeRIP-seq:(Medium) rs200452382 Functional Loss SNV dbSNP153 33..33 33 - - - 60069 RMVar_ID_60069 Human_SNP_ID_106204690 m1A Human chr2 - 189001580 189001580 189001580 TTGAGAATGTCTTTAACACTTACAGGGCTACCACGAGGTCCAGCTATACCTGGAAGTCCGGGGGC TTGAGAATGTCTTTAACACTTACAGGGCTACCGCGAGGTCCAGCTATACCTGGAAGTCCGGGGGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:189001526..189001600 26863196 MeRIP-seq:(Medium) rs759951500 Functional Loss SNV dbSNP153 33..33 33 - - - 60070 RMVar_ID_60070 Human_SNP_ID_106205037 m1A Human chr2 - 189002952 189002952 189002952 TCCTTTACCACCAGGTTCACCATTCTGTCCCTACATGCAACAACAACAGCAATCTCTCAGCTGAC TCCTTTACCACCAGGTTCACCATTCTGTCCCTGCATGCAACAACAACAGCAATCTCTCAGCTGAC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:189002951..189003025 26863196 MeRIP-seq:(Medium) rs1325362291 Functional Loss SNV dbSNP153 33..33 33 - - - 60071 RMVar_ID_60071 Human_SNP_ID_106205048 m1A Human chr2 + 189002988 189002988 189002988 GACAGAATGGTGAACCTGGTGGTAAAGGAGAAAGAGGGGCTCCGGGTGAGAAAGGTGAAGGAGGC GACAGAATGGTGAACCTGGTGGTAAAGGAGAAGGAGGGGCTCCGGGTGAGAAAGGTGAAGGAGGC A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:189002951..189003075 26863196 MeRIP-seq:(Medium) rs1309388302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336334,Human_Splice_Rec_336335,Human_Splice_Rec_336434 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_114363,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205216,RMVar_hsa_circ_205219,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_109126,RMVar_hsa_circ_66984,RMVar_hsa_circ_82223,RMVar_hsa_circ_205233,RMVar_hsa_circ_80204,RMVar_hsa_circ_205234,RMVar_hsa_circ_205235,RMVar_hsa_circ_125639,RMVar_hsa_circ_310216,RMVar_hsa_circ_91505,RMVar_hsa_circ_205236,RMVar_hsa_circ_205237,RMVar_hsa_circ_107947,RMVar_hsa_circ_205239,RMVar_hsa_circ_60713,RMVar_hsa_circ_205238 60072 RMVar_ID_60072 Human_SNP_ID_106205393 m1A Human chr2 - 189004056 189004056 189004056 TTTGGTCCAGACACTCCAGGGCTGCCAGGAGCACCAGTGTTACCCGCAGGACCTGGGGGCCCATC TTTGGTCCAGACACTCCAGGGCTGCCAGGAGCGCCAGTGTTACCCGCAGGACCTGGGGGCCCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:189003976..189004172;chr2:189003945..189004082 26863196 MeRIP-seq:(Medium) rs1179979349 Functional Loss SNV dbSNP153 33..33 33 - - - 60073 RMVar_ID_60073 Human_SNP_ID_106207734 m1A Human chr2 + 189011630 189011630 189011630 TGATCATGTACATTTTGTCCTTTTTTACAGAAACACACTGGGGAATGGAGCAAAACAGTCTTTGA TGATCATGTACATTTTGTCCTTTTTTACAGAAGCACACTGGGGAATGGAGCAAAACAGTCTTTGA A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:189011626..189011700 32194978 MeRIP-seq:(Medium) rs754723643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_336364,Human_Splice_Rec_336442,Human_Splice_Rec_336458 RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_205240,RMVar_hsa_circ_124579,RMVar_hsa_circ_205241,RMVar_hsa_circ_127071,RMVar_hsa_circ_109084,RMVar_hsa_circ_205243 60074 RMVar_ID_60074 Human_SNP_ID_106214874 m1A Human chr2 + 189039552 189039534 189039552 GGGGGACCCGGAGGGCCAGGTGGGCCAGGCTCACCAGGAGGGCCCTAATTAAAAAGAGATTGGAA GGGGGACCCGGAGGG__________________CCAGGAGGGCCCTAATTAAAAAGAGATTGGAA GCCAGGTGGGCCAGGCTCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:189039501..189054225 32194978 MeRIP-seq:(Medium) rs1553512960 Functional Loss DEL dbSNP153 16..33 33 - - - 60075 RMVar_ID_60075 Human_SNP_ID_106219031 m1A Human chr2 + 189057024 189057024 189057024 GCTGTGCCTTCAGCACCTTTTTCTCCTATGCCACCCTGGGAAAACACACAAAATACAATTGATTC GCTGTGCCTTCAGCACCTTTTTCTCCTATGCCGCCCTGGGAAAACACACAAAATACAATTGATTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:189056976..189057050 32194978 MeRIP-seq:(Medium) rs994797617 Functional Loss SNV dbSNP153 33..33 33 - - - 60076 RMVar_ID_60076 Human_SNP_ID_106219032 m1A Human chr2 + 189057024 189057024 189057024 GCTGTGCCTTCAGCACCTTTTTCTCCTATGCCACCCTGGGAAAACACACAAAATACAATTGATTC GCTGTGCCTTCAGCACCTTTTTCTCCTATGCCTCCCTGGGAAAACACACAAAATACAATTGATTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:189056976..189057050 32194978 MeRIP-seq:(Medium) rs994797617 Functional Loss SNV dbSNP153 33..33 33 - - - 60077 RMVar_ID_60077 Human_SNP_ID_106224248 m1A Human chr2 + 189078567 189078567 189078567 AGTCTCCCTCTCTCTCCTGGCATTCCCCTCGGACCCTATAGACGATAGAGAAGAAATGTCTCTTG AGTCTCCCTCTCTCTCCTGGCATTCCCCTCGGGCCCTATAGACGATAGAGAAGAAATGTCTCTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:189056951..189110274 32194978 MeRIP-seq:(Medium) rs751477421 Functional Loss SNV dbSNP153 33..33 33 - - - 60078 RMVar_ID_60078 Human_SNP_ID_106246729 m1A Human chr2 + 189179750 189179750 189179750 CTCTGCAAACCCCCTTTTTCAGCACCAGCTCCAGCACAGTCTGCGAAAACTTTTTTCAAGCGATG CTCTGCAAACCCCCTTTTTCAGCACCAGCTCCCGCACAGTCTGCGAAAACTTTTTTCAAGCGATG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:189179701..189179750 32194978 MeRIP-seq:(Medium) rs1433555150 Functional Loss SNV dbSNP153 33..33 33 - - - 60079 RMVar_ID_60079 Human_SNP_ID_106246730 m1A Human chr2 + 189179750 189179750 189179750 CTCTGCAAACCCCCTTTTTCAGCACCAGCTCCAGCACAGTCTGCGAAAACTTTTTTCAAGCGATG CTCTGCAAACCCCCTTTTTCAGCACCAGCTCCTGCACAGTCTGCGAAAACTTTTTTCAAGCGATG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:189179701..189179750 32194978 MeRIP-seq:(Medium) rs1433555150 Functional Loss SNV dbSNP153 33..33 33 - - - 60080 RMVar_ID_60080 Human_SNP_ID_106305747 m1A Human chr2 - 189441518 189441518 189441518 TAAAGTTCAACTCGCTGCCGCCACAACGAACCACGCGGATGTTCTCCTCCTCCACCATCTTTGCG TAAAGTTCAACTCGCTGCCGCCACAACGAACCGCGCGGATGTTCTCCTCCTCCACCATCTTTGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:189441469..189441751 26863196 MeRIP-seq:(Medium) rs369077081 Functional Loss SNV dbSNP153 33..33 33 - - - 60081 RMVar_ID_60081 Human_SNP_ID_106305755 m1A Human chr2 - 189441528 189441528 189441528 ACAGCTCTCCTAAAGTTCAACTCGCTGCCGCCACAACGAACCACGCGGATGTTCTCCTCCTCCAC ACAGCTCTCCTAAAGTTCAACTCGCTGCCGCCGCAACGAACCACGCGGATGTTCTCCTCCTCCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:189441482..189448432 26863196 MeRIP-seq:(Medium) rs760256469 Functional Loss SNV dbSNP153 33..33 33 - - - 60082 RMVar_ID_60082 Human_SNP_ID_106305760 m1A Human chr2 + 189441535 189441535 189441535 AGGAGAACATCCGCGTGGTTCGTTGTGGCGGCAGCGAGTTGAACTTTAGGAGAGCTGTGTTCTCT AGGAGAACATCCGCGTGGTTCGTTGTGGCGGCGGCGAGTTGAACTTTAGGAGAGCTGTGTTCTCT A G WDR75 Ensembl:ENSG00000115368 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:189441485..189441610 26863196 MeRIP-seq:(Medium) rs75534935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1905727,Human_RBP_ID_4625610,Human_RBP_ID_5588851,Human_RBP_ID_9959697,Human_RBP_ID_13716398,Human_RBP_ID_18421963,Human_RBP_ID_18751449,Human_RBP_ID_22986264,Human_RBP_ID_23212147,Human_RBP_ID_23843699 Human_Splice_Rec_336693,Human_Splice_Rec_336735,Human_Splice_Rec_336743,Human_Splice_Rec_336749,Human_Splice_Rec_336789,Human_Splice_Rec_336829 60083 RMVar_ID_60083 Human_SNP_ID_106305764 m1A Human chr2 + 189441539 189441539 189441539 GAACATCCGCGTGGTTCGTTGTGGCGGCAGCGAGTTGAACTTTAGGAGAGCTGTGTTCTCTGCAG GAACATCCGCGTGGTTCGTTGTGGCGGCAGCGTGTTGAACTTTAGGAGAGCTGTGTTCTCTGCAG A T WDR75 Ensembl:ENSG00000115368 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:189441490..189441616 26863196 MeRIP-seq:(Medium) rs1336878148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1905727,Human_RBP_ID_4625610,Human_RBP_ID_5588851,Human_RBP_ID_9959697,Human_RBP_ID_13716398,Human_RBP_ID_18421963,Human_RBP_ID_18751449,Human_RBP_ID_22986264,Human_RBP_ID_23212147,Human_RBP_ID_23843699 Human_Splice_Rec_336693,Human_Splice_Rec_336735,Human_Splice_Rec_336743,Human_Splice_Rec_336749,Human_Splice_Rec_336789,Human_Splice_Rec_336829 60084 RMVar_ID_60084 Human_SNP_ID_106381421 m1A Human chr2 + 189762731 189762731 189762731 GCAGTAGCTAGCACTTGTCTCCTTTCCCTACTAAAGACTGTCGACTGCCCTTATCGCTGCAGGAG GCAGTAGCTAGCACTTGTCTCCTTTCCCTACTGAAGACTGTCGACTGCCCTTATCGCTGCAGGAG A G OSGEPL1-AS1 Ensembl:ENSG00000253559 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:189761661..189762730 26863196 MeRIP-seq:(Medium) rs898860703 Functional Loss SNV dbSNP153 33..33 33 - - - 60085 RMVar_ID_60085 Human_SNP_ID_106383710 m1A Human chr2 - 189771751 189771751 189771751 GAATTAATAAGTATTGAAATGTTTTGAAACTGAAAAAAAATTTTACAGCTACTGAATTTCTTATA GAATTAATAAGTATTGAAATGTTTTGAAACTGGAAAAAAATTTTACAGCTACTGAATTTCTTATA T C ORMDL1 Ensembl:ENSG00000128699 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1429105605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_540514,Human_RBP_ID_1905874,Human_RBP_ID_9099670,Human_RBP_ID_22998344,Human_RBP_ID_23843918 60086 RMVar_ID_60086 Human_SNP_ID_106386429 m1A Human chr2 - 189783893 189783893 189783893 CCGTCTTCGGAGGCACCGGCGAGGGCAGAGCCAACAGCCTCTTCACGGTCTGTAAGGTCATTGTT CCGTCTTCGGAGGCACCGGCGAGGGCAGAGCCCACAGCCTCTTCACGGTCTGTAAGGTCATTGTT T G ORMDL1 Ensembl:ENSG00000128699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:189783891..189784029 26863196 MeRIP-seq:(Medium) rs1204844869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622797,Human_RBP_ID_9428884,Human_RBP_ID_18422421,Human_RBP_ID_19102263,Human_RBP_ID_23119495 RMVar_hsa_circ_88204,RMVar_hsa_circ_205327 60087 RMVar_ID_60087 Human_SNP_ID_106475852 m1A Human chr2 + 190158998 190158998 190158998 GGATGAGGATGCAGGAAGTTGATTAGCAAGGGATTAGGATTCCAAAGGCTGCAGTGGAAGGGGCT GGATGAGGATGCAGGAAGTTGATTAGCAAGGGGTTAGGATTCCAAAGGCTGCAGTGGAAGGGGCT A G C2orf88 Ensembl:ENSG00000187699 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:190158977..190159104 26863196 MeRIP-seq:(Medium) rs1475202009 Functional Loss SNV dbSNP153 33..33 33 - - - 60088 RMVar_ID_60088 Human_SNP_ID_106488283 m1A Human chr2 + 190210202 190210202 190210202 TCCCATTTTTCCTCTCCAACTTACTACACTCTAACTTCTGCCCCCACTCCTCTAAAATGGCTTGC TCCCATTTTTCCTCTCCAACTTACTACACTCTGACTTCTGCCCCCACTCCTCTAAAATGGCTTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:190210152..190210453 26863196 MeRIP-seq:(Medium) rs1172459809 Functional Loss SNV dbSNP153 33..33 33 - - - 60089 RMVar_ID_60089 Human_SNP_ID_106499292 m1A Human chr2 - 190253840 190253840 190253840 CTGCTGAGGCTCTGGGGCAGGAATGAGTGTAGAATGTTAGGGAACTGAAAGAAGACCAGAGTGGC CTGCTGAGGCTCTGGGGCAGGAATGAGTGTAGGATGTTAGGGAACTGAAAGAAGACCAGAGTGGC T C HIBCH Ensembl:ENSG00000198130 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:190253830..190253996 26863196 MeRIP-seq:(Medium) rs976823303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13719951,Human_RBP_ID_23844154 RMVar_hsa_circ_119683,RMVar_hsa_circ_205353,RMVar_hsa_circ_73037,RMVar_hsa_circ_335509,RMVar_hsa_circ_337194,RMVar_hsa_circ_359923,RMVar_hsa_circ_102400,RMVar_hsa_circ_115990,RMVar_hsa_circ_205356,RMVar_hsa_circ_205357,RMVar_hsa_circ_375880,RMVar_hsa_circ_205358,RMVar_hsa_circ_128065,RMVar_hsa_circ_205360,RMVar_hsa_circ_205362,RMVar_hsa_circ_82706,RMVar_hsa_circ_205361,RMVar_hsa_circ_205359 60090 RMVar_ID_60090 Human_SNP_ID_106503787 m1A Human chr2 - 190271175 190271175 190271175 TGATGGATTGTATGTGATGGATAAAGTGGAGCAAGAATGACTTTCAGGTGTCTAGGCTGGGCCAT TGATGGATTGTATGTGATGGATAAAGTGGAGCGAGAATGACTTTCAGGTGTCTAGGCTGGGCCAT T C HIBCH Ensembl:ENSG00000198130 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:190271173..190271265 26863196 MeRIP-seq:(Medium) rs112441119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8507807,Human_RBP_ID_13719997,Human_RBP_ID_23844168 RMVar_hsa_circ_119683,RMVar_hsa_circ_205353,RMVar_hsa_circ_337194,RMVar_hsa_circ_359923,RMVar_hsa_circ_20660,RMVar_hsa_circ_102400,RMVar_hsa_circ_115990,RMVar_hsa_circ_205357,RMVar_hsa_circ_375880,RMVar_hsa_circ_205358,RMVar_hsa_circ_128065,RMVar_hsa_circ_205360,RMVar_hsa_circ_205361,RMVar_hsa_circ_205359,RMVar_hsa_circ_205363,RMVar_hsa_circ_12686 60091 RMVar_ID_60091 Human_SNP_ID_106516106 m1A Human chr2 + 190319681 190319681 190319681 GGCCCTTTTCCCACTGTGGCGAGTGCCGCTGAAGAGCCTGCCCTTGGCCCCTCGCTCTCTCACTC GGCCCTTTTCCCACTGTGGCGAGTGCCGCTGAGGAGCCTGCCCTTGGCCCCTCGCTCTCTCACTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:190319673..190319785 26863196 MeRIP-seq:(Medium) rs775286873 Functional Loss SNV dbSNP153 33..33 33 - - - 60092 RMVar_ID_60092 Human_SNP_ID_106521494 m1A Human chr2 + 190343844 190343844 190343844 CGTCCTCTGGCCGCGCCTGCGGCCGCACGCCCAGCGCCCCTCGCCTAACCTCGCGCCCGGGCCGC CGTCCTCTGGCCGCGCCTGCGGCCGCACGCCCCGCGCCCCTCGCCTAACCTCGCGCCCGGGCCGC A C INPP1 Ensembl:ENSG00000151689 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:190343747..190343884 26863410 MeRIP-seq:(Medium) rs1290890376 Functional Loss SNV dbSNP153 33..33 33 - - - 60093 RMVar_ID_60093 Human_SNP_ID_106521495 m1A Human chr2 + 190343844 190343844 190343844 CGTCCTCTGGCCGCGCCTGCGGCCGCACGCCCAGCGCCCCTCGCCTAACCTCGCGCCCGGGCCGC CGTCCTCTGGCCGCGCCTGCGGCCGCACGCCCGGCGCCCCTCGCCTAACCTCGCGCCCGGGCCGC A G INPP1 Ensembl:ENSG00000151689 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:190343747..190343884 26863410 MeRIP-seq:(Medium) rs1290890376 Functional Loss SNV dbSNP153 33..33 33 - - - 60094 RMVar_ID_60094 Human_SNP_ID_106536685 m1A Human chr2 - 190408394 190408371 190408394 GCGCCGGGGCGGCGGCTGTCGGGGCAGCGCGCACCATCCCGGGCTGCTCGCGCGCTCCTCCGGGG GCGCCGGGGCGGCGGCTGTCGGGGCAGCGCGC_______________________TCCTCCGGGG AGCGCGCGAGCAGCCCGGGATGGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:190408194..190408453 26863196 MeRIP-seq:(Medium) rs1387050004 Functional Loss DEL dbSNP153 33..55 33 - - - 60095 RMVar_ID_60095 Human_SNP_ID_106536697 m1A Human chr2 - 190408394 190408394 190408394 GCGCCGGGGCGGCGGCTGTCGGGGCAGCGCGCACCATCCCGGGCTGCTCGCGCGCTCCTCCGGGG GCGCCGGGGCGGCGGCTGTCGGGGCAGCGCGCTCCATCCCGGGCTGCTCGCGCGCTCCTCCGGGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:190408194..190408453 26863196 MeRIP-seq:(Medium) rs1441105357 Functional Loss SNV dbSNP153 33..33 33 - - - 60096 RMVar_ID_60096 Human_SNP_ID_106538276 m1A Human chr2 - 190415250 190415250 190415250 AATAAAAATAAAAAAGATAGATACTTTAACATACATACCATACCAATAATTTTTAAAATGGAAAT AATAAAAATAAAAAAGATAGATACTTTAACATGCATACCATACCAATAATTTTTAAAATGGAAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:190415242..190415326 26863196 MeRIP-seq:(Medium) rs1012351304 Functional Loss SNV dbSNP153 33..33 33 - - - 60097 RMVar_ID_60097 Human_SNP_ID_106564983 m1A Human chr2 - 190534656 190534656 190534656 GGCTCGGGTCGCACGGAGCTGACCCCTAACGAAATGGGGCCGCGCCAAGGGCGGTGGTGGCTGCT GGCTCGGGTCGCACGGAGCTGACCCCTAACGACATGGGGCCGCGCCAAGGGCGGTGGTGGCTGCT T G NEMP2 Ensembl:ENSG00000189362 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:190534605..190534813 26863196 MeRIP-seq:(Medium) rs1299592814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624918,Human_RBP_ID_18422426 Human_Splice_Rec_337903,Human_Splice_Rec_337941 RMVar_hsa_circ_102197,RMVar_hsa_circ_205372 60098 RMVar_ID_60098 Human_SNP_ID_106565157 m1A Human chr2 + 190535035 190535035 190535035 CGCTGCCCTCGGCGCAGGGGTGGGAGTTGCAGAGAGGAAGAGTCGCTAACCCGGAGTGTTTCTTA CGCTGCCCTCGGCGCAGGGGTGGGAGTTGCAGCGAGGAAGAGTCGCTAACCCGGAGTGTTTCTTA A C AC108047.1 Ensembl:ENSG00000233654 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:190534899..190535034 26863196 MeRIP-seq:(Medium) rs1048850330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258951 Human_Splice_Rec_337959 60099 RMVar_ID_60099 Human_SNP_ID_106591401 m1A Human chr2 - 190656037 190656037 190656037 CATTCAAAAGCTAACTCGGAGGCCTTGCTGCCAATGTACAGCAACTTCCACTTCCACTTCCATCA CATTCAAAAGCTAACTCGGAGGCCTTGCTGCCCATGTACAGCAACTTCCACTTCCACTTCCATCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:190656035..190656136 32194978 MeRIP-seq:(Medium) rs928069388 Functional Loss SNV dbSNP153 33..33 33 - - - 60100 RMVar_ID_60100 Human_SNP_ID_106643175 m1A Human chr2 + 190880875 190880874 190880875 GAAGAGAACCGGTCGCGGCAATCCTAGCGCGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC GAAGAGAACCGGTCGCGGCAATCCTAGCGCGC_GCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC CA C GLS Ensembl:ENSG00000115419 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:190880826..190881226;chr2:190880826..190881129;chr2:190880826..190881234;chr2:190880826..190881138 26863196 MeRIP-seq:(Medium) rs1367921864 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5195883,Human_RBP_ID_9347780,Human_RBP_ID_18421973 60101 RMVar_ID_60101 Human_SNP_ID_106643283 m1A Human chr2 - 190880927 190880927 190880927 GGGTGTGGTTCCGGCTCGGACTCCCGCAGCGGATGCGGGTGCTGCTGCTGCTGCTGCTGCTGCTG GGGTGTGGTTCCGGCTCGGACTCCCGCAGCGGCTGCGGGTGCTGCTGCTGCTGCTGCTGCTGCTG T G AC005540.1 Ensembl:ENSG00000235852 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:190880826..190881000 26863410 MeRIP-seq:(Medium) rs1476345352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5199056 Human_miRNA_ID_3155621,Human_miRNA_ID_3155969,Human_miRNA_ID_3156318,Human_miRNA_ID_3184823,Human_miRNA_ID_3193201 60102 RMVar_ID_60102 Human_SNP_ID_106643291 m1A Human chr2 - 190880940 190880939 190880940 AGGGCAGCTACTTGGGTGTGGTTCCGGCTCGGACTCCCGCAGCGGATGCGGGTGCTGCTGCTGCT AGGGCAGCTACTTGGGTGTGGTTCCGGCTCGG_CTCCCGCAGCGGATGCGGGTGCTGCTGCTGCT GT G AC005540.1 Ensembl:ENSG00000235852 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:190880893..190880990 32194978 MeRIP-seq:(Medium) rs1328628910 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5199056 Human_miRNA_ID_3205299 60103 RMVar_ID_60103 Human_SNP_ID_106643564 m1A Human chr2 + 190881434 190881434 190881434 GGACGGCCCCGGGGAGACGGACGCGTTTGGCAACAGCGAGGGCAAAGAGCTGGTGGCCTCAGGTG GGACGGCCCCGGGGAGACGGACGCGTTTGGCAGCAGCGAGGGCAAAGAGCTGGTGGCCTCAGGTG A G GLS Ensembl:ENSG00000115419 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:190881279..190881522 32194978 MeRIP-seq:(Medium) rs550215381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919026,Human_RBP_ID_4590367,Human_RBP_ID_9960355,Human_RBP_ID_19002752,Human_RBP_ID_22076737,Human_RBP_ID_22450632,Human_RBP_ID_27285044 Human_Splice_Rec_338071,Human_Splice_Rec_338105,Human_Splice_Rec_338133,Human_Splice_Rec_338135 60104 RMVar_ID_60104 Human_SNP_ID_106643586 m1A Human chr2 - 190881476 190881476 190881476 AAGGAACGAGGCCTCCTGCGCCTCGCGGAGACACTCACTTTTCACCTGAGGCCACCAGCTCTTTG AAGGAACGAGGCCTCCTGCGCCTCGCGGAGACGCTCACTTTTCACCTGAGGCCACCAGCTCTTTG T C AC005540.1 Ensembl:ENSG00000235852 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:190881472..190881914 32194978 MeRIP-seq:(Medium) rs1272641938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_338070 60105 RMVar_ID_60105 Human_SNP_ID_106660401 m1A Human chr2 - 190951162 190951154 190951162 CTTCCTCCTGTTTGCTGCTTTGCAGATTCATTACCCACTTTCCACTGCCAAATACTACTCCCAAG CTTCCTCCTGTTTGCTGCTTTGCAGATTCATT________TCCACTGCCAAATACTACTCCCAAG AAAGTGGGT A STAT1 Ensembl:ENSG00000115415 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:190950972..190951200 26863196 MeRIP-seq:(Medium) rs1209003971 Functional Loss DEL dbSNP153 33..40 33 - - - 60106 RMVar_ID_60106 Human_SNP_ID_106660405 m1A Human chr2 - 190951162 190951162 190951162 CTTCCTCCTGTTTGCTGCTTTGCAGATTCATTACCCACTTTCCACTGCCAAATACTACTCCCAAG CTTCCTCCTGTTTGCTGCTTTGCAGATTCATTGCCCACTTTCCACTGCCAAATACTACTCCCAAG T C STAT1 Ensembl:ENSG00000115415 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:190950972..190951200 26863196 MeRIP-seq:(Medium) rs968416133 Functional Loss SNV dbSNP153 33..33 33 - - - 60107 RMVar_ID_60107 Human_SNP_ID_106675595 m1A Human chr2 + 191013570 191013570 191013570 CCCCAACAAGGGCCTGGGGATTCAACCAAAGGAGCAGCTACGCACAGCACGTTAGGTGCCAAGAC CCCCAACAAGGGCCTGGGGATTCAACCAAAGGGGCAGCTACGCACAGCACGTTAGGTGCCAAGAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:191009933..191013569 32194978 MeRIP-seq:(Medium) rs1215740346 Functional Loss SNV dbSNP153 33..33 33 - - - 60108 RMVar_ID_60108 Human_SNP_ID_106742464 m1A Human chr2 + 191307976 191307976 191307976 CTGTTCACCAACCTAGATCCCTCCATCTCCCCAAAAAAACAGAATTGTGTTCAAATTTTTGTAAC CTGTTCACCAACCTAGATCCCTCCATCTCCCCCAAAAAACAGAATTGTGTTCAAATTTTTGTAAC A C MYO1B Ensembl:ENSG00000128641 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:191307941..191308068 26863196 MeRIP-seq:(Medium) rs145527722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126354,RMVar_hsa_circ_355832,RMVar_hsa_circ_205433,RMVar_hsa_circ_357084,RMVar_hsa_circ_352897,RMVar_hsa_circ_63836,RMVar_hsa_circ_375792,RMVar_hsa_circ_205436 60109 RMVar_ID_60109 Human_SNP_ID_106742465 m1A Human chr2 + 191307976 191307976 191307976 CTGTTCACCAACCTAGATCCCTCCATCTCCCCAAAAAAACAGAATTGTGTTCAAATTTTTGTAAC CTGTTCACCAACCTAGATCCCTCCATCTCCCCGAAAAAACAGAATTGTGTTCAAATTTTTGTAAC A G MYO1B Ensembl:ENSG00000128641 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:191307941..191308068 26863196 MeRIP-seq:(Medium) rs145527722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126354,RMVar_hsa_circ_355832,RMVar_hsa_circ_205433,RMVar_hsa_circ_357084,RMVar_hsa_circ_352897,RMVar_hsa_circ_63836,RMVar_hsa_circ_375792,RMVar_hsa_circ_205436 60110 RMVar_ID_60110 Human_SNP_ID_106761589 m1A Human chr2 + 191390427 191390427 191390427 AGGGCAGGCTACGCCTTCAGGCAGGCCTATGAACCTTGCCTAGAAAGATACAAAATGCTTTGTAA AGGGCAGGCTACGCCTTCAGGCAGGCCTATGACCCTTGCCTAGAAAGATACAAAATGCTTTGTAA A C MYO1B Ensembl:ENSG00000128641 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:191390377..191390478 32194978 MeRIP-seq:(Medium) rs1559226494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_339523,Human_Splice_Rec_339579,Human_Splice_Rec_339639,Human_Splice_Rec_339739 RMVar_hsa_circ_266790,RMVar_hsa_circ_358443,RMVar_hsa_circ_68677,RMVar_hsa_circ_33933,RMVar_hsa_circ_66706,RMVar_hsa_circ_61381,RMVar_hsa_circ_56592,RMVar_hsa_circ_29103,RMVar_hsa_circ_60783,RMVar_hsa_circ_39096,RMVar_hsa_circ_66783,RMVar_hsa_circ_69286,RMVar_hsa_circ_205445,RMVar_hsa_circ_70196,RMVar_hsa_circ_205446,RMVar_hsa_circ_123006,RMVar_hsa_circ_70498,RMVar_hsa_circ_367031,RMVar_hsa_circ_22028,RMVar_hsa_circ_205447 60111 RMVar_ID_60111 Human_SNP_ID_106764981 m1A Human chr2 - 191402585 191402585 191402585 ATAGTAAATAAAAGAGACAGCCCAATGCAGACAGCACAAATGACCAGAAAAAGATATCCCACCAA ATAGTAAATAAAAGAGACAGCCCAATGCAGACGGCACAAATGACCAGAAAAAGATATCCCACCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:191402581..191402661 26863196 MeRIP-seq:(Medium) rs977657057 Functional Loss SNV dbSNP153 33..33 33 - - - 60112 RMVar_ID_60112 Human_SNP_ID_106829987 m1A Human chr2 + 191678213 191678213 191678213 CCGTTTCGCTGTCACAGCCCGTTCCTTCCCGGAGCCCGGGACAGGCTGGGCGCGCGCCCGTGTGA CCGTTTCGCTGTCACAGCCCGTTCCTTCCCGGGGCCCGGGACAGGCTGGGCGCGCGCCCGTGTGA A G NABP1 Ensembl:ENSG00000173559 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:191678165..191678319 26863196 MeRIP-seq:(Medium) rs893922245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623773 Human_Splice_Rec_339807,Human_Splice_Rec_339811,Human_Splice_Rec_339823,Human_Splice_Rec_339851,Human_Splice_Rec_339861,Human_Splice_Rec_339885,Human_Splice_Rec_339903 60113 RMVar_ID_60113 Human_SNP_ID_737722159 m1A Human chrM + 263 263 263 CATAATAATAACAATTGAATGTCTGCACAGCCACTTTCCACACAGACATCATAACAAAAAATTTC CATAATAATAACAATTGAATGTCTGCACAGCCGCTTTCCACACAGACATCATAACAAAAAATTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrMT:31..337;chrMT:29..337 26863196 MeRIP-seq:(Medium) rs2853515 Functional Loss SNV dbSNP153 33..33 33 - - - 60114 RMVar_ID_60114 Human_SNP_ID_737722160 m1A Human chrM + 272 272 272 AACAATTGAATGTCTGCACAGCCACTTTCCACACAGACATCATAACAAAAAATTTCCACCAAACC AACAATTGAATGTCTGCACAGCCACTTTCCACGCAGACATCATAACAAAAAATTTCCACCAAACC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrMT:43..400 26863196 MeRIP-seq:(Medium) rs1556422410 Functional Loss SNV dbSNP153 33..33 33 - - - 60115 RMVar_ID_60115 Human_SNP_ID_737722162 m1A Human chrM - 279 279 279 GAGGGGGGGTTTGGTGGAAATTTTTTGTTATGATGTCTGTGTGGAAAGTGGCTGTGCAGACATTC GAGGGGGGGTTTGGTGGAAATTTTTTGTTATGGTGTCTGTGTGGAAAGTGGCTGTGCAGACATTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrMT:182..389 26863196 MeRIP-seq:(Medium) rs879199276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271424,Human_RBP_ID_287387,Human_RBP_ID_723300,Human_RBP_ID_1060098,Human_RBP_ID_1120077,Human_RBP_ID_1228309,Human_RBP_ID_1340269,Human_RBP_ID_1404203,Human_RBP_ID_1708422,Human_RBP_ID_2067442,Human_RBP_ID_3233494,Human_RBP_ID_3911710,Human_RBP_ID_5044730,Human_RBP_ID_5230420,Human_RBP_ID_5277756,Human_RBP_ID_5454879,Human_RBP_ID_5482702,Human_RBP_ID_5516751,Human_RBP_ID_5637204,Human_RBP_ID_7959671,Human_RBP_ID_8161326,Human_RBP_ID_8276599,Human_RBP_ID_8709477,Human_RBP_ID_8931310,Human_RBP_ID_16770906,Human_RBP_ID_17057576,Human_RBP_ID_17202758,Human_RBP_ID_17439365,Human_RBP_ID_17551308,Human_RBP_ID_17717189,Human_RBP_ID_18142185,Human_RBP_ID_18212794,Human_RBP_ID_18400815,Human_RBP_ID_18453859,Human_RBP_ID_18521671,Human_RBP_ID_18912746,Human_RBP_ID_21764144,Human_RBP_ID_22342631,Human_RBP_ID_22518719,Human_RBP_ID_22839187,Human_RBP_ID_23096013,Human_RBP_ID_23142034,Human_RBP_ID_23201902,Human_RBP_ID_24317903,Human_RBP_ID_24443860,Human_RBP_ID_24524713,Human_RBP_ID_26245330,Human_RBP_ID_26567192,Human_RBP_ID_26740539,Human_RBP_ID_27140400,Human_RBP_ID_27162910,Human_RBP_ID_27377507,Human_RBP_ID_27548325,Human_RBP_ID_27570853,Human_RBP_ID_27788315 60116 RMVar_ID_60116 Human_SNP_ID_737722187 m1A Human chrM - 318 317 319 TGGCAGAGATGTGTTTAAGTGCTGTGGCCAGAAGCGGGGGAGGGGGGGTTTGGTGGAAATTTTTT TGGCAGAGATGTGTTTAAGTGCTGTGGCCAG__GCGGGGGAGGGGGGGTTTGGTGGAAATTTTTT CTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEK293T,untreat control chrMT:176..404;chrMT:214..410;chrMT:220..426 26863410 MeRIP-seq:(Medium) rs1556422427 Functional Loss DEL dbSNP153 32..33 33 - - - 60117 RMVar_ID_60117 Human_SNP_ID_737722315 m1A Human chrM + 827 827 827 AGCCACACCCCCACGGGAAACAGCAGTGATTAACCTTTAGCAATAAACGAAAGTTTAACTAAGCT AGCCACACCCCCACGGGAAACAGCAGTGATTAGCCTTTAGCAATAAACGAAAGTTTAACTAAGCT A G MT-RNR1 Ensembl:ENSG00000211459 Other exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrMT:816..1306 26863410 MeRIP-seq:(Medium) rs28358569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186032,Human_RBP_ID_287501,Human_RBP_ID_723437,Human_RBP_ID_1120099,Human_RBP_ID_1228639,Human_RBP_ID_1340345,Human_RBP_ID_1404332,Human_RBP_ID_1708931,Human_RBP_ID_2067709,Human_RBP_ID_3233647,Human_RBP_ID_3911941,Human_RBP_ID_5091123,Human_RBP_ID_5271883,Human_RBP_ID_5310224,Human_RBP_ID_5482742,Human_RBP_ID_5516831,Human_RBP_ID_7959997,Human_RBP_ID_8161392,Human_RBP_ID_8226394,Human_RBP_ID_8276711,Human_RBP_ID_8709857,Human_RBP_ID_8731530,Human_RBP_ID_8931522,Human_RBP_ID_9241271,Human_RBP_ID_9315989,Human_RBP_ID_10443590,Human_RBP_ID_16771305,Human_RBP_ID_17065898,Human_RBP_ID_17177721,Human_RBP_ID_17202848,Human_RBP_ID_17324080,Human_RBP_ID_17439437,Human_RBP_ID_17551503,Human_RBP_ID_17717241,Human_RBP_ID_18142317,Human_RBP_ID_18203934,Human_RBP_ID_18212986,Human_RBP_ID_18453895,Human_RBP_ID_18521798,Human_RBP_ID_18542809,Human_RBP_ID_21763624,Human_RBP_ID_21957319,Human_RBP_ID_22120187,Human_RBP_ID_22342701,Human_RBP_ID_22518787,Human_RBP_ID_22839831,Human_RBP_ID_23096203,Human_RBP_ID_23142109,Human_RBP_ID_24318158,Human_RBP_ID_26245562,Human_RBP_ID_26567402,Human_RBP_ID_26740621,Human_RBP_ID_26752715,Human_RBP_ID_26796962,Human_RBP_ID_27140362,Human_RBP_ID_27163039,Human_RBP_ID_27377607,Human_RBP_ID_27548517,Human_RBP_ID_27570884,Human_RBP_ID_27788486 Clinvar_Rec_203 60118 RMVar_ID_60118 Human_SNP_ID_737722320 m1A Human chrM + 896 896 896 TAACCCCAGGGTTGGTCAATTTCGTGCCAGCCACCGCGGTCACACGATTAACCCAAGTCAATAGA TAACCCCAGGGTTGGTCAATTTCGTGCCAGCCGCCGCGGTCACACGATTAACCCAAGTCAATAGA A G MT-RNR1 Ensembl:ENSG00000211459 Other exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chrMT:885..1220 26863410 MeRIP-seq:(Medium) rs1556422491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723463,Human_RBP_ID_1228679,Human_RBP_ID_3233959,Human_RBP_ID_3911962,Human_RBP_ID_5091124,Human_RBP_ID_5244313,Human_RBP_ID_5516834,Human_RBP_ID_5637245,Human_RBP_ID_5659259,Human_RBP_ID_8276728,Human_RBP_ID_8709927,Human_RBP_ID_8731517,Human_RBP_ID_9315990,Human_RBP_ID_16771306,Human_RBP_ID_17057684,Human_RBP_ID_17202895,Human_RBP_ID_17324103,Human_RBP_ID_17551555,Human_RBP_ID_17717263,Human_RBP_ID_18521866,Human_RBP_ID_18542851,Human_RBP_ID_21957330,Human_RBP_ID_22518815,Human_RBP_ID_22839831,Human_RBP_ID_24318246,Human_RBP_ID_26796960,Human_RBP_ID_27140362,Human_RBP_ID_27163103,Human_RBP_ID_27377651,Human_RBP_ID_27548518 60119 RMVar_ID_60119 Human_SNP_ID_737722329 m1A Human chrM + 955 955 955 AATAGAAGCCGGCGTAAAGAGTGTTTTAGATCACCCCCTCCCCAATAAAGCTAAAACTCACCTGA AATAGAAGCCGGCGTAAAGAGTGTTTTAGATCCCCCCCTCCCCAATAAAGCTAAAACTCACCTGA A C MT-RNR1 Ensembl:ENSG00000211459 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chrMT:576..1061;chrMT:626..1062;chrMT:640..1084 26863196 MeRIP-seq:(Medium) rs1556422497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271359,Human_RBP_ID_287448,Human_RBP_ID_723463,Human_RBP_ID_798946,Human_RBP_ID_847905,Human_RBP_ID_966189,Human_RBP_ID_1060109,Human_RBP_ID_1120104,Human_RBP_ID_1228694,Human_RBP_ID_1340357,Human_RBP_ID_1404346,Human_RBP_ID_1708969,Human_RBP_ID_2067734,Human_RBP_ID_3233694,Human_RBP_ID_3911962,Human_RBP_ID_5044988,Human_RBP_ID_5091124,Human_RBP_ID_5230505,Human_RBP_ID_5251961,Human_RBP_ID_5310225,Human_RBP_ID_5431663,Human_RBP_ID_5454907,Human_RBP_ID_5482746,Human_RBP_ID_5516834,Human_RBP_ID_5637245,Human_RBP_ID_5641223,Human_RBP_ID_5659259,Human_RBP_ID_7960087,Human_RBP_ID_8161477,Human_RBP_ID_8226396,Human_RBP_ID_8276759,Human_RBP_ID_8709927,Human_RBP_ID_8731531,Human_RBP_ID_8931498,Human_RBP_ID_9241302,Human_RBP_ID_9264869,Human_RBP_ID_9315990,Human_RBP_ID_9341892,Human_RBP_ID_9443082,Human_RBP_ID_10443644,Human_RBP_ID_10486106,Human_RBP_ID_16771306,Human_RBP_ID_17057654,Human_RBP_ID_17065910,Human_RBP_ID_17095703,Human_RBP_ID_17177726,Human_RBP_ID_17202895,Human_RBP_ID_17210603,Human_RBP_ID_17324103,Human_RBP_ID_17439460,Human_RBP_ID_17551555,Human_RBP_ID_17579878,Human_RBP_ID_17586465,Human_RBP_ID_17587057,Human_RBP_ID_17587317,Human_RBP_ID_17644587,Human_RBP_ID_17672652,Human_RBP_ID_17717251,Human_RBP_ID_18142340,Human_RBP_ID_18173713,Human_RBP_ID_18186007,Human_RBP_ID_18203946,Human_RBP_ID_18213001,Human_RBP_ID_18453886,Human_RBP_ID_18508113,Human_RBP_ID_18521833,Human_RBP_ID_18542834,Human_RBP_ID_18545117,Human_RBP_ID_18912896,Human_RBP_ID_18927613,Human_RBP_ID_18963338,Human_RBP_ID_19148119,Human_RBP_ID_21763633,Human_RBP_ID_21957232,Human_RBP_ID_21997193,Human_RBP_ID_22342742,Human_RBP_ID_22368870,Human_RBP_ID_22372701,Human_RBP_ID_22412348,Human_RBP_ID_22424983,Human_RBP_ID_22518795,Human_RBP_ID_22530939,Human_RBP_ID_22531872,Human_RBP_ID_22556928,Human_RBP_ID_22692271,Human_RBP_ID_22706393,Human_RBP_ID_22734120,Human_RBP_ID_22748489,Human_RBP_ID_22777546,Human_RBP_ID_22839831,Human_RBP_ID_23096279,Human_RBP_ID_23117360,Human_RBP_ID_23120962,Human_RBP_ID_23142128,Human_RBP_ID_23202059,Human_RBP_ID_23301030,Human_RBP_ID_23317191,Human_RBP_ID_24318246,Human_RBP_ID_24443878,Human_RBP_ID_24524762,Human_RBP_ID_24537882,Human_RBP_ID_24549883,Human_RBP_ID_24555679,Human_RBP_ID_24563803,Human_RBP_ID_26245623,Human_RBP_ID_26567480,Human_RBP_ID_26740642,Human_RBP_ID_26752723,Human_RBP_ID_26796960,Human_RBP_ID_27140362,Human_RBP_ID_27163103,Human_RBP_ID_27377662,Human_RBP_ID_27548518,Human_RBP_ID_27574953,Human_RBP_ID_27788471 60120 RMVar_ID_60120 Human_SNP_ID_737722384 m1A Human chrM + 1299 1299 1299 TCTTCAGCAAACCCTGATGAAGGCTACAAAGTAAGCGCAAGTACCCACGTAAAGACGTTAGGTCA TCTTCAGCAAACCCTGATGAAGGCTACAAAGTGAGCGCAAGTACCCACGTAAAGACGTTAGGTCA A G MT-RNR1 Ensembl:ENSG00000211459 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1556422518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723145,Human_RBP_ID_966190,Human_RBP_ID_1708533,Human_RBP_ID_2067510,Human_RBP_ID_5045076,Human_RBP_ID_5230506,Human_RBP_ID_5659260,Human_RBP_ID_8276441,Human_RBP_ID_8709510,Human_RBP_ID_9241055,Human_RBP_ID_9264852,Human_RBP_ID_9443083,Human_RBP_ID_10486107,Human_RBP_ID_16770382,Human_RBP_ID_17550998,Human_RBP_ID_17579879,Human_RBP_ID_17717258,Human_RBP_ID_18203638,Human_RBP_ID_18212600,Human_RBP_ID_18521555,Human_RBP_ID_18542574,Human_RBP_ID_18912612,Human_RBP_ID_19148120,Human_RBP_ID_21764456,Human_RBP_ID_22531873,Human_RBP_ID_22556929,Human_RBP_ID_24317606,Human_RBP_ID_24537898,Human_RBP_ID_24555680,Human_RBP_ID_26752749,Human_RBP_ID_27162711,Human_RBP_ID_27548066,Human_RBP_ID_27574943 60121 RMVar_ID_60121 Human_SNP_ID_737722395 m1A Human chrM + 1379 1379 1379 GGTGGCAAGAAATGGGCTACATTTTCTACCCCAGAAAACTACGATAGCCCTTATGAAACTTAAGG GGTGGCAAGAAATGGGCTACATTTTCTACCCCCGAAAACTACGATAGCCCTTATGAAACTTAAGG A C MT-RNR1 Ensembl:ENSG00000211459 Other exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrMT:1256..1541 26863196 MeRIP-seq:(Medium) rs28729254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271248,Human_RBP_ID_287358,Human_RBP_ID_723173,Human_RBP_ID_847907,Human_RBP_ID_966191,Human_RBP_ID_1060093,Human_RBP_ID_1228376,Human_RBP_ID_1340178,Human_RBP_ID_1404102,Human_RBP_ID_1708593,Human_RBP_ID_2067534,Human_RBP_ID_3233247,Human_RBP_ID_3911750,Human_RBP_ID_5044476,Human_RBP_ID_5091125,Human_RBP_ID_5230507,Human_RBP_ID_5244329,Human_RBP_ID_5271778,Human_RBP_ID_5516680,Human_RBP_ID_5637173,Human_RBP_ID_7959395,Human_RBP_ID_8161415,Human_RBP_ID_8276478,Human_RBP_ID_8709570,Human_RBP_ID_8931178,Human_RBP_ID_9241085,Human_RBP_ID_9341894,Human_RBP_ID_9355200,Human_RBP_ID_10443359,Human_RBP_ID_10486015,Human_RBP_ID_16770479,Human_RBP_ID_17057476,Human_RBP_ID_17065771,Human_RBP_ID_17177661,Human_RBP_ID_17202621,Human_RBP_ID_17323906,Human_RBP_ID_17439281,Human_RBP_ID_17551100,Human_RBP_ID_17668024,Human_RBP_ID_17717133,Human_RBP_ID_18142027,Human_RBP_ID_18173722,Human_RBP_ID_18185947,Human_RBP_ID_18203690,Human_RBP_ID_18212625,Human_RBP_ID_18453838,Human_RBP_ID_18521581,Human_RBP_ID_18542629,Human_RBP_ID_18545119,Human_RBP_ID_18912649,Human_RBP_ID_21763516,Human_RBP_ID_21957584,Human_RBP_ID_22120056,Human_RBP_ID_22342557,Human_RBP_ID_22368872,Human_RBP_ID_22412267,Human_RBP_ID_22518679,Human_RBP_ID_22531874,Human_RBP_ID_22556929,Human_RBP_ID_22748466,Human_RBP_ID_22839427,Human_RBP_ID_23095783,Human_RBP_ID_23141943,Human_RBP_ID_23201785,Human_RBP_ID_23301035,Human_RBP_ID_23317245,Human_RBP_ID_24317666,Human_RBP_ID_24524663,Human_RBP_ID_24555681,Human_RBP_ID_26245081,Human_RBP_ID_26567062,Human_RBP_ID_26740454,Human_RBP_ID_27140179,Human_RBP_ID_27162758,Human_RBP_ID_27377406,Human_RBP_ID_27548144,Human_RBP_ID_27574958,Human_RBP_ID_27788325 60122 RMVar_ID_60122 Human_SNP_ID_737722654 m1A Human chrM + 3243 3243 3243 CCACCCAAGAACAGGGTTTGTTAAGATGGCAGAGCCCGGTAATCGCATAAAACTTAAAACTTTAC CCACCCAAGAACAGGGTTTGTTAAGATGGCAGGGCCCGGTAATCGCATAAAACTTAAAACTTTAC A G MT-TL1 Ensembl:ENSG00000209082 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs199474657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271306,Human_RBP_ID_287416,Human_RBP_ID_723353,Human_RBP_ID_1120186,Human_RBP_ID_1228533,Human_RBP_ID_1248109,Human_RBP_ID_1340287,Human_RBP_ID_1404231,Human_RBP_ID_1708809,Human_RBP_ID_2067644,Human_RBP_ID_3233510,Human_RBP_ID_3911873,Human_RBP_ID_5045262,Human_RBP_ID_5230426,Human_RBP_ID_5244633,Human_RBP_ID_5271862,Human_RBP_ID_5277748,Human_RBP_ID_5482716,Human_RBP_ID_5516769,Human_RBP_ID_5637222,Human_RBP_ID_7959776,Human_RBP_ID_8161337,Human_RBP_ID_8276628,Human_RBP_ID_8709768,Human_RBP_ID_8931349,Human_RBP_ID_9241200,Human_RBP_ID_16770974,Human_RBP_ID_17057603,Human_RBP_ID_17065852,Human_RBP_ID_17177701,Human_RBP_ID_17202776,Human_RBP_ID_17324017,Human_RBP_ID_17551351,Human_RBP_ID_17717275,Human_RBP_ID_18142239,Human_RBP_ID_18185991,Human_RBP_ID_18203836,Human_RBP_ID_18212830,Human_RBP_ID_18453869,Human_RBP_ID_18521693,Human_RBP_ID_18542756,Human_RBP_ID_18912790,Human_RBP_ID_19148094,Human_RBP_ID_21763577,Human_RBP_ID_22120136,Human_RBP_ID_22342650,Human_RBP_ID_22518743,Human_RBP_ID_22839706,Human_RBP_ID_23096050,Human_RBP_ID_23142070,Human_RBP_ID_23201921,Human_RBP_ID_23301073,Human_RBP_ID_23317139,Human_RBP_ID_24318031,Human_RBP_ID_24443883,Human_RBP_ID_24524728,Human_RBP_ID_26245392,Human_RBP_ID_26567297,Human_RBP_ID_26740558,Human_RBP_ID_26752851,Human_RBP_ID_26796947,Human_RBP_ID_27140291,Human_RBP_ID_27162956,Human_RBP_ID_27377539,Human_RBP_ID_27548366,Human_RBP_ID_27788421 Clinvar_Rec_204 60123 RMVar_ID_60123 Human_SNP_ID_737722661 m1A Human chrM + 3260 3260 3260 TTGTTAAGATGGCAGAGCCCGGTAATCGCATAAAACTTAAAACTTTACAGTCAGAGGTTCAATTC TTGTTAAGATGGCAGAGCCCGGTAATCGCATAGAACTTAAAACTTTACAGTCAGAGGTTCAATTC A G MT-TL1 Ensembl:ENSG00000209082 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs199474663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271306,Human_RBP_ID_287416,Human_RBP_ID_723353,Human_RBP_ID_798919,Human_RBP_ID_1060100,Human_RBP_ID_1146855,Human_RBP_ID_1228533,Human_RBP_ID_1248110,Human_RBP_ID_1340287,Human_RBP_ID_1404231,Human_RBP_ID_1708809,Human_RBP_ID_2067644,Human_RBP_ID_3233510,Human_RBP_ID_3911873,Human_RBP_ID_5044754,Human_RBP_ID_5091100,Human_RBP_ID_5230427,Human_RBP_ID_5244479,Human_RBP_ID_5271862,Human_RBP_ID_5277748,Human_RBP_ID_5310209,Human_RBP_ID_5431611,Human_RBP_ID_5482716,Human_RBP_ID_5516769,Human_RBP_ID_5659236,Human_RBP_ID_7959776,Human_RBP_ID_8161338,Human_RBP_ID_8239514,Human_RBP_ID_8276628,Human_RBP_ID_8709768,Human_RBP_ID_8731518,Human_RBP_ID_8931349,Human_RBP_ID_9241200,Human_RBP_ID_9264829,Human_RBP_ID_9315929,Human_RBP_ID_10443502,Human_RBP_ID_10486082,Human_RBP_ID_16770974,Human_RBP_ID_17057604,Human_RBP_ID_17065852,Human_RBP_ID_17095678,Human_RBP_ID_17177701,Human_RBP_ID_17202776,Human_RBP_ID_17210595,Human_RBP_ID_17324017,Human_RBP_ID_17439380,Human_RBP_ID_17551352,Human_RBP_ID_17586431,Human_RBP_ID_17672628,Human_RBP_ID_17717214,Human_RBP_ID_18142239,Human_RBP_ID_18185991,Human_RBP_ID_18203836,Human_RBP_ID_18212832,Human_RBP_ID_18400818,Human_RBP_ID_18453870,Human_RBP_ID_18521693,Human_RBP_ID_18542756,Human_RBP_ID_18912790,Human_RBP_ID_19148094,Human_RBP_ID_21764179,Human_RBP_ID_21957175,Human_RBP_ID_22120136,Human_RBP_ID_22342650,Human_RBP_ID_22368844,Human_RBP_ID_22372680,Human_RBP_ID_22412313,Human_RBP_ID_22518743,Human_RBP_ID_22530922,Human_RBP_ID_22706394,Human_RBP_ID_22734094,Human_RBP_ID_22748462,Human_RBP_ID_22777518,Human_RBP_ID_22839706,Human_RBP_ID_23096050,Human_RBP_ID_23142071,Human_RBP_ID_23300974,Human_RBP_ID_23317140,Human_RBP_ID_24318031,Human_RBP_ID_24443872,Human_RBP_ID_24524730,Human_RBP_ID_24537878,Human_RBP_ID_24540794,Human_RBP_ID_24555660,Human_RBP_ID_26245392,Human_RBP_ID_26567528,Human_RBP_ID_26740558,Human_RBP_ID_26796947,Human_RBP_ID_27140291,Human_RBP_ID_27377539,Human_RBP_ID_27548366,Human_RBP_ID_27570863,Human_RBP_ID_27788422 Clinvar_Rec_205 60124 RMVar_ID_60124 Human_SNP_ID_737722671 m1A Human chrM + 3289 3289 3289 ATAAAACTTAAAACTTTACAGTCAGAGGTTCAATTCCTCTTCTTAACAACATACCCATGGCCAAC ATAAAACTTAAAACTTTACAGTCAGAGGTTCAGTTCCTCTTCTTAACAACATACCCATGGCCAAC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1569483871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1228542,Human_RBP_ID_1708817,Human_RBP_ID_2067647,Human_RBP_ID_3911877,Human_RBP_ID_7959793,Human_RBP_ID_8276630,Human_RBP_ID_16771004,Human_RBP_ID_18521697,Human_RBP_ID_22839715,Human_RBP_ID_23096064,Human_RBP_ID_27162959 60125 RMVar_ID_60125 Human_SNP_ID_737722729 m1A Human chrM + 3511 3511 3511 AAGAGCCCCTAAAACCCGCCACATCTACCATCACCCTCTACATCACCGCCCCGACCTTAGCTCTC AAGAGCCCCTAAAACCCGCCACATCTACCATCGCCCTCTACATCACCGCCCCGACCTTAGCTCTC A G MT-ND1 Ensembl:ENSG00000198888 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrMT:3393..4168 26863410 MeRIP-seq:(Medium) rs386828909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287485,Human_RBP_ID_723364,Human_RBP_ID_798904,Human_RBP_ID_1228545,Human_RBP_ID_1708810,Human_RBP_ID_2067649,Human_RBP_ID_3233522,Human_RBP_ID_3911879,Human_RBP_ID_5244486,Human_RBP_ID_5431614,Human_RBP_ID_5482720,Human_RBP_ID_5516783,Human_RBP_ID_7959810,Human_RBP_ID_8239517,Human_RBP_ID_8709768,Human_RBP_ID_8931364,Human_RBP_ID_9241208,Human_RBP_ID_16771024,Human_RBP_ID_17057611,Human_RBP_ID_17065856,Human_RBP_ID_17095611,Human_RBP_ID_17202784,Human_RBP_ID_17324024,Human_RBP_ID_17439382,Human_RBP_ID_17551668,Human_RBP_ID_18203843,Human_RBP_ID_18212841,Human_RBP_ID_18521706,Human_RBP_ID_18912801,Human_RBP_ID_21763581,Human_RBP_ID_22412314,Human_RBP_ID_22424997,Human_RBP_ID_22839706,Human_RBP_ID_23096075,Human_RBP_ID_26245407,Human_RBP_ID_26567308,Human_RBP_ID_26752633,Human_RBP_ID_27140298,Human_RBP_ID_27162967,Human_RBP_ID_27377543,Human_RBP_ID_27548383 60126 RMVar_ID_60126 Human_SNP_ID_737722781 m1A Human chrM + 3721 3721 3721 CCCTGATCGGCGCACTGCGAGCAGTAGCCCAAACAATCTCATATGAAGTCACCCTAGCCATCATT CCCTGATCGGCGCACTGCGAGCAGTAGCCCAAGCAATCTCATATGAAGTCACCCTAGCCATCATT A G MT-ND1 Ensembl:ENSG00000198888 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrMT:3698..4194 26863410 MeRIP-seq:(Medium) rs878927280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723372,Human_RBP_ID_798907,Human_RBP_ID_1228548,Human_RBP_ID_1404245,Human_RBP_ID_1708830,Human_RBP_ID_2067650,Human_RBP_ID_3233539,Human_RBP_ID_3911884,Human_RBP_ID_7959830,Human_RBP_ID_8276648,Human_RBP_ID_8709788,Human_RBP_ID_9241216,Human_RBP_ID_10443517,Human_RBP_ID_16771044,Human_RBP_ID_17202785,Human_RBP_ID_17324030,Human_RBP_ID_17551621,Human_RBP_ID_18212861,Human_RBP_ID_18521712,Human_RBP_ID_18542899,Human_RBP_ID_18912803,Human_RBP_ID_21763584,Human_RBP_ID_22412318,Human_RBP_ID_22518750,Human_RBP_ID_22839738,Human_RBP_ID_23096644,Human_RBP_ID_23317148,Human_RBP_ID_24318061,Human_RBP_ID_26245422,Human_RBP_ID_26567316,Human_RBP_ID_26740568,Human_RBP_ID_27140304,Human_RBP_ID_27377548,Human_RBP_ID_27788426 60127 RMVar_ID_60127 Human_SNP_ID_737723005 m1A Human chrM + 4918 4918 4918 CTCAATCATATACCAAATCTCTCCCTCACTAAACGTAAGCCTTCTCCTCACTCTCTCAATCTTAT CTCAATCATATACCAAATCTCTCCCTCACTAAGCGTAAGCCTTCTCCTCACTCTCTCAATCTTAT A G MT-ND2 Ensembl:ENSG00000198763 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrMT:4801..5062 26863196 MeRIP-seq:(Medium) rs879058895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723393,Human_RBP_ID_1228574,Human_RBP_ID_1404269,Human_RBP_ID_1708854,Human_RBP_ID_3233562,Human_RBP_ID_5431628,Human_RBP_ID_7959875,Human_RBP_ID_8709813,Human_RBP_ID_10443926,Human_RBP_ID_16771142,Human_RBP_ID_17057619,Human_RBP_ID_17202811,Human_RBP_ID_17551406,Human_RBP_ID_18203871,Human_RBP_ID_18213246,Human_RBP_ID_18521739,Human_RBP_ID_21763592,Human_RBP_ID_22412321,Human_RBP_ID_22839764,Human_RBP_ID_23096108,Human_RBP_ID_23317157,Human_RBP_ID_24393823,Human_RBP_ID_26245453,Human_RBP_ID_26567349,Human_RBP_ID_26740584,Human_RBP_ID_27377573,Human_RBP_ID_27548427 60128 RMVar_ID_60128 Human_SNP_ID_737723119 m1A Human chrM + 5520 5520 5520 CCCCTTTTATACTAATAATCTTATAGAAATTTAGGTTAAATACAGACCAAGAGCCTTCAAAGCCC CCCCTTTTATACTAATAATCTTATAGAAATTTGGGTTAAATACAGACCAAGAGCCTTCAAAGCCC A G MT-TW Ensembl:ENSG00000210117 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs878974649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22412331,Human_RBP_ID_26567371 60129 RMVar_ID_60129 Human_SNP_ID_737723185 m1A Human chrM + 5823 5823 5823 GAATTTGCAATTCAATATGAAAATCACCTCGGAGCTGGTAAAAAGAGGCCTAACCCCTGTCTTTA GAATTTGCAATTCAATATGAAAATCACCTCGGGGCTGGTAAAAAGAGGCCTAACCCCTGTCTTTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chrMT:5751..5900;chrMT:5751..5875 26863196,32194978 MeRIP-seq:(Medium) rs878875817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723411,Human_RBP_ID_1228590,Human_RBP_ID_1404285,Human_RBP_ID_1708880,Human_RBP_ID_3233597,Human_RBP_ID_3911911,Human_RBP_ID_5271842,Human_RBP_ID_7959913,Human_RBP_ID_8161368,Human_RBP_ID_8276679,Human_RBP_ID_8709834,Human_RBP_ID_8931399,Human_RBP_ID_9241244,Human_RBP_ID_16771224,Human_RBP_ID_17203043,Human_RBP_ID_17551425,Human_RBP_ID_18142286,Human_RBP_ID_18203884,Human_RBP_ID_18212906,Human_RBP_ID_18912828,Human_RBP_ID_21763600,Human_RBP_ID_22342683,Human_RBP_ID_22518761,Human_RBP_ID_22839795,Human_RBP_ID_23096143,Human_RBP_ID_23201967,Human_RBP_ID_23317296,Human_RBP_ID_24318121,Human_RBP_ID_26752675,Human_RBP_ID_27163015,Human_RBP_ID_27377586 60130 RMVar_ID_60130 Human_SNP_ID_737723189 m1A Human chrM + 5836 5836 5836 AATATGAAAATCACCTCGGAGCTGGTAAAAAGAGGCCTAACCCCTGTCTTTAGATTTACAGTCCA AATATGAAAATCACCTCGGAGCTGGTAAAAAGGGGCCTAACCCCTGTCTTTAGATTTACAGTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrMT:5751..5900 26863196 MeRIP-seq:(Medium) rs386828979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287428,Human_RBP_ID_723413,Human_RBP_ID_1228590,Human_RBP_ID_1404285,Human_RBP_ID_1708880,Human_RBP_ID_3233597,Human_RBP_ID_3911911,Human_RBP_ID_7959913,Human_RBP_ID_8161368,Human_RBP_ID_8276679,Human_RBP_ID_8709834,Human_RBP_ID_9241244,Human_RBP_ID_16771224,Human_RBP_ID_17203043,Human_RBP_ID_17551425,Human_RBP_ID_18142286,Human_RBP_ID_18203885,Human_RBP_ID_18212910,Human_RBP_ID_18912828,Human_RBP_ID_21763600,Human_RBP_ID_22518761,Human_RBP_ID_22839795,Human_RBP_ID_23096143,Human_RBP_ID_23201967,Human_RBP_ID_23317296,Human_RBP_ID_26752675,Human_RBP_ID_27377586 60131 RMVar_ID_60131 Human_SNP_ID_737723249 m1A Human chrM + 6252 6252 6252 CTCCCTCTCTCCTACTCCTGCTCGCATCTGCTATAGTGGAGGCCGGAGCAGGAACAGGTTGAACA CTCCCTCTCTCCTACTCCTGCTCGCATCTGCTGTAGTGGAGGCCGGAGCAGGAACAGGTTGAACA A G MT-CO1 Ensembl:ENSG00000198804 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrMT:6201..6700 32194978 MeRIP-seq:(Medium) rs878927119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271335,Human_RBP_ID_723423,Human_RBP_ID_798859,Human_RBP_ID_1228599,Human_RBP_ID_1708886,Human_RBP_ID_3233605,Human_RBP_ID_5230445,Human_RBP_ID_5244367,Human_RBP_ID_5431640,Human_RBP_ID_5637229,Human_RBP_ID_7959930,Human_RBP_ID_8161372,Human_RBP_ID_8239530,Human_RBP_ID_8276688,Human_RBP_ID_8709846,Human_RBP_ID_8931405,Human_RBP_ID_10443560,Human_RBP_ID_16771251,Human_RBP_ID_17057630,Human_RBP_ID_17202836,Human_RBP_ID_17439412,Human_RBP_ID_17551436,Human_RBP_ID_18203894,Human_RBP_ID_18212914,Human_RBP_ID_18521754,Human_RBP_ID_18912834,Human_RBP_ID_21763604,Human_RBP_ID_22342690,Human_RBP_ID_22518766,Human_RBP_ID_22839802,Human_RBP_ID_23096146,Human_RBP_ID_23142096,Human_RBP_ID_23201977,Human_RBP_ID_23317165,Human_RBP_ID_24318134,Human_RBP_ID_26245496,Human_RBP_ID_26567382,Human_RBP_ID_26740598,Human_RBP_ID_26752677,Human_RBP_ID_27140351,Human_RBP_ID_27163024,Human_RBP_ID_27377595,Human_RBP_ID_27548455,Human_RBP_ID_27788440 60132 RMVar_ID_60132 Human_SNP_ID_737723306 m1A Human chrM + 6494 6494 6494 TCCGTCCTAATCACAGCAGTCCTACTTCTCCTATCTCTCCCAGTCCTAGCTGCTGGCATCACTAT TCCGTCCTAATCACAGCAGTCCTACTTCTCCTGTCTCTCCCAGTCCTAGCTGCTGGCATCACTAT A G MT-CO1 Ensembl:ENSG00000198804 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrMT:5994..6647 26863410 MeRIP-seq:(Medium) rs878937838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287431,Human_RBP_ID_723429,Human_RBP_ID_798863,Human_RBP_ID_1120094,Human_RBP_ID_1228601,Human_RBP_ID_1248126,Human_RBP_ID_1340318,Human_RBP_ID_1404292,Human_RBP_ID_1708894,Human_RBP_ID_2067688,Human_RBP_ID_3233921,Human_RBP_ID_3911919,Human_RBP_ID_5044860,Human_RBP_ID_5431645,Human_RBP_ID_5482735,Human_RBP_ID_5516817,Human_RBP_ID_7959952,Human_RBP_ID_8161378,Human_RBP_ID_8276698,Human_RBP_ID_8709849,Human_RBP_ID_8931415,Human_RBP_ID_9241255,Human_RBP_ID_10443579,Human_RBP_ID_16771251,Human_RBP_ID_17057790,Human_RBP_ID_17095653,Human_RBP_ID_17203046,Human_RBP_ID_17324057,Human_RBP_ID_17439414,Human_RBP_ID_17551449,Human_RBP_ID_17717232,Human_RBP_ID_18142294,Human_RBP_ID_18203898,Human_RBP_ID_18212923,Human_RBP_ID_18453876,Human_RBP_ID_18521760,Human_RBP_ID_18542789,Human_RBP_ID_18912846,Human_RBP_ID_21763605,Human_RBP_ID_21957186,Human_RBP_ID_22120172,Human_RBP_ID_22342696,Human_RBP_ID_22412336,Human_RBP_ID_22839821,Human_RBP_ID_23096155,Human_RBP_ID_23201987,Human_RBP_ID_23300963,Human_RBP_ID_24318150,Human_RBP_ID_24524750,Human_RBP_ID_26245504,Human_RBP_ID_26567390,Human_RBP_ID_26740602,Human_RBP_ID_26752681,Human_RBP_ID_27140356,Human_RBP_ID_27163032,Human_RBP_ID_27377598,Human_RBP_ID_27548462,Human_RBP_ID_27788443 60133 RMVar_ID_60133 Human_SNP_ID_737723391 m1A Human chrM - 6939 6938 6939 AATGCCAGTCAGGCCACCTACGGTGAAAAGAAAGATGAATCCTAGGGCTCAGAGCACTGCAGCAG AATGCCAGTCAGGCCACCTACGGTGAAAAGAA_GATGAATCCTAGGGCTCAGAGCACTGCAGCAG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrMT:6895..6977 26863196 MeRIP-seq:(Medium) rs1569484126 Functional Loss DEL dbSNP153 33..33 33 - - - 60134 RMVar_ID_60134 Human_SNP_ID_737723422 m1A Human chrM + 7146 7146 7146 CCCTAGACCAAACCTACGCCAAAATCCATTTCACTATCATATTCATCGGCGTAAATCTAACTTTC CCCTAGACCAAACCTACGCCAAAATCCATTTCGCTATCATATTCATCGGCGTAAATCTAACTTTC A G MT-CO1 Ensembl:ENSG00000198804 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrMT:7122..7352 26863196 MeRIP-seq:(Medium) rs372136420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271342,Human_RBP_ID_287433,Human_RBP_ID_723452,Human_RBP_ID_1228621,Human_RBP_ID_1340332,Human_RBP_ID_1404309,Human_RBP_ID_1708912,Human_RBP_ID_2067699,Human_RBP_ID_3233621,Human_RBP_ID_5230601,Human_RBP_ID_7959986,Human_RBP_ID_8161382,Human_RBP_ID_8276712,Human_RBP_ID_8709865,Human_RBP_ID_8931437,Human_RBP_ID_9241432,Human_RBP_ID_9264835,Human_RBP_ID_16771341,Human_RBP_ID_17057793,Human_RBP_ID_17202855,Human_RBP_ID_17324074,Human_RBP_ID_17439427,Human_RBP_ID_17551474,Human_RBP_ID_17717236,Human_RBP_ID_18142308,Human_RBP_ID_18203909,Human_RBP_ID_18212947,Human_RBP_ID_18400820,Human_RBP_ID_18521781,Human_RBP_ID_18542801,Human_RBP_ID_18912862,Human_RBP_ID_21763613,Human_RBP_ID_22342706,Human_RBP_ID_22839847,Human_RBP_ID_23096704,Human_RBP_ID_23202000,Human_RBP_ID_23301091,Human_RBP_ID_24318177,Human_RBP_ID_26245539,Human_RBP_ID_26567416,Human_RBP_ID_26752690,Human_RBP_ID_27140372,Human_RBP_ID_27377616,Human_RBP_ID_27548485,Human_RBP_ID_27788450 60135 RMVar_ID_60135 Human_SNP_ID_737723423 m1A Human chrM - 7148 7148 7148 AAGAAAGTTAGATTTACGCCGATGAATATGATAGTGAAATGGATTTTGGCGTAGGTTTGGTCTAG AAGAAAGTTAGATTTACGCCGATGAATATGATGGTGAAATGGATTTTGGCGTAGGTTTGGTCTAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrMT:7121..7349;chrMT:7076..7333 26863196 MeRIP-seq:(Medium) rs1556423240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7959987,Human_RBP_ID_16771340,Human_RBP_ID_18521782,Human_RBP_ID_21764307,Human_RBP_ID_22839850,Human_RBP_ID_23096705,Human_RBP_ID_24537866,Human_RBP_ID_27140373 60136 RMVar_ID_60136 Human_SNP_ID_737723433 m1A Human chrM + 7241 7241 7241 ATGCCCCGACGTTACTCGGACTACCCCGATGCATACACCACATGAAACATCCTATCATCTGTAGG ATGCCCCGACGTTACTCGGACTACCCCGATGCGTACACCACATGAAACATCCTATCATCTGTAGG A G MT-CO1 Ensembl:ENSG00000198804 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrMT:7131..7324 26863196 MeRIP-seq:(Medium) rs879201845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271447,Human_RBP_ID_723455,Human_RBP_ID_798866,Human_RBP_ID_1228623,Human_RBP_ID_1340333,Human_RBP_ID_1404310,Human_RBP_ID_1708917,Human_RBP_ID_2067701,Human_RBP_ID_3233626,Human_RBP_ID_3911931,Human_RBP_ID_5044890,Human_RBP_ID_5230456,Human_RBP_ID_5244378,Human_RBP_ID_5637233,Human_RBP_ID_7959991,Human_RBP_ID_8276714,Human_RBP_ID_8709866,Human_RBP_ID_8931441,Human_RBP_ID_9241266,Human_RBP_ID_16771357,Human_RBP_ID_17203049,Human_RBP_ID_17324077,Human_RBP_ID_17439429,Human_RBP_ID_17551480,Human_RBP_ID_18203914,Human_RBP_ID_18212953,Human_RBP_ID_18521784,Human_RBP_ID_18542803,Human_RBP_ID_18912863,Human_RBP_ID_21763614,Human_RBP_ID_22342708,Human_RBP_ID_22839853,Human_RBP_ID_23096195,Human_RBP_ID_23202003,Human_RBP_ID_23317177,Human_RBP_ID_26245544,Human_RBP_ID_26567423,Human_RBP_ID_26740612,Human_RBP_ID_26752696,Human_RBP_ID_27140376,Human_RBP_ID_27163203,Human_RBP_ID_27377619,Human_RBP_ID_27548491 60137 RMVar_ID_60137 Human_SNP_ID_737723457 m1A Human chrM + 7375 7375 7375 AAAAGTCCTAATAGTAGAAGAACCCTCCATAAACCTGGAGTGACTATATGGATGCCCCCCACCCT AAAAGTCCTAATAGTAGAAGAACCCTCCATAAGCCTGGAGTGACTATATGGATGCCCCCCACCCT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1556423274 Functional Loss SNV dbSNP153 33..33 33 - - - 60138 RMVar_ID_60138 Human_SNP_ID_737723495 m1A Human chrM + 7526 7526 7526 CATGGCCTCCATGACTTTTTCAAAAAGGTATTAGAAAAACCATTTCATAACTTTGTCAAAGTTAA CATGGCCTCCATGACTTTTTCAAAAAGGTATTGGAAAAACCATTTCATAACTTTGTCAAAGTTAA A G MT-TD Ensembl:ENSG00000210154 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs121434454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186021,Human_RBP_ID_1404313,Human_RBP_ID_1708924,Human_RBP_ID_2067705,Human_RBP_ID_3233636,Human_RBP_ID_5244643,Human_RBP_ID_5271878,Human_RBP_ID_5637257,Human_RBP_ID_8276795,Human_RBP_ID_8709875,Human_RBP_ID_9341885,Human_RBP_ID_17439495,Human_RBP_ID_18142380,Human_RBP_ID_18521865,Human_RBP_ID_18542852,Human_RBP_ID_18545111,Human_RBP_ID_22777511,Human_RBP_ID_24555655 Clinvar_Rec_206 60139 RMVar_ID_60139 Human_SNP_ID_737723498 m1A Human chrM + 7570 7570 7570 TCATAACTTTGTCAAAGTTAAATTATAGGCTAAATCCTATATATCTTAATGGCACATGCAGCGCA TCATAACTTTGTCAAAGTTAAATTATAGGCTAGATCCTATATATCTTAATGGCACATGCAGCGCA A G MT-TD Ensembl:ENSG00000210154 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1556423311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637257 60140 RMVar_ID_60140 Human_SNP_ID_737723653 m1A Human chrM + 8348 8348 8348 TTAACCTTTTAAGTTAAAGATTAAGAGAACCAACACCTCTTTACAGTGAAATGCCCCAACTAAAT TTAACCTTTTAAGTTAAAGATTAAGAGAACCAGCACCTCTTTACAGTGAAATGCCCCAACTAAAT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1556423430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2928404 60141 RMVar_ID_60141 Human_SNP_ID_737723691 m1A Human chrM + 8483 8483 8483 TAAACACAAACTACCACCTACCTCCCTCACCAAAGCCCATAAAAATAAAAAATTATAACAAACCC TAAACACAAACTACCACCTACCTCCCTCACCAGAGCCCATAAAAATAAAAAATTATAACAAACCC A G MT-ATP8 Ensembl:ENSG00000228253 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs377093295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287493,Human_RBP_ID_723484,Human_RBP_ID_1120102,Human_RBP_ID_1228672,Human_RBP_ID_1248133,Human_RBP_ID_1340348,Human_RBP_ID_1404336,Human_RBP_ID_1708959,Human_RBP_ID_2067724,Human_RBP_ID_3233674,Human_RBP_ID_3911952,Human_RBP_ID_8161473,Human_RBP_ID_8239541,Human_RBP_ID_8276751,Human_RBP_ID_8709914,Human_RBP_ID_8931484,Human_RBP_ID_9241435,Human_RBP_ID_16771498,Human_RBP_ID_17057644,Human_RBP_ID_17095635,Human_RBP_ID_17202888,Human_RBP_ID_17324099,Human_RBP_ID_17439454,Human_RBP_ID_17551636,Human_RBP_ID_17586434,Human_RBP_ID_17717245,Human_RBP_ID_18142330,Human_RBP_ID_18203936,Human_RBP_ID_18212988,Human_RBP_ID_18521821,Human_RBP_ID_21763626,Human_RBP_ID_21957249,Human_RBP_ID_22518791,Human_RBP_ID_22839909,Human_RBP_ID_23096238,Human_RBP_ID_23301094,Human_RBP_ID_23317309,Human_RBP_ID_24318242,Human_RBP_ID_26245597,Human_RBP_ID_26567468,Human_RBP_ID_26740632,Human_RBP_ID_26752882,Human_RBP_ID_27163092,Human_RBP_ID_27377645,Human_RBP_ID_27548534 60142 RMVar_ID_60142 Human_SNP_ID_737723708 m1A Human chrM - 8540 8540 8540 CTAGGATTGTGGGGGCAATGAATGAAGCGAACAGATTTTCGTTCATTTTGGTTCTCAGGGTTTGT CTAGGATTGTGGGGGCAATGAATGAAGCGAACGGATTTTCGTTCATTTTGGTTCTCAGGGTTTGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chrMT:8389..8775;chrMT:8379..8757 26863196 MeRIP-seq:(Medium) rs878852987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1404338,Human_RBP_ID_5637244,Human_RBP_ID_16771495,Human_RBP_ID_18521823,Human_RBP_ID_23096743,Human_RBP_ID_24318245 Clinvar_Rec_207,Clinvar_Rec_1493 60143 RMVar_ID_60143 Human_SNP_ID_737723746 m1A Human chrM + 8659 8659 8659 CCAAATATCTCATCAACAACCGACTAATCACCACCCAACAATGACTAATCAAACTAACCTCAAAA CCAAATATCTCATCAACAACCGACTAATCACCGCCCAACAATGACTAATCAAACTAACCTCAAAA A G MT-ATP6 Ensembl:ENSG00000198899 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrMT:8434..8767 26863196 MeRIP-seq:(Medium) rs879150284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271355,Human_RBP_ID_287488,Human_RBP_ID_723487,Human_RBP_ID_798910,Human_RBP_ID_1228674,Human_RBP_ID_1340350,Human_RBP_ID_1404339,Human_RBP_ID_1708964,Human_RBP_ID_2067727,Human_RBP_ID_3233680,Human_RBP_ID_3911957,Human_RBP_ID_5230463,Human_RBP_ID_5482744,Human_RBP_ID_5516839,Human_RBP_ID_7960068,Human_RBP_ID_8161395,Human_RBP_ID_8276756,Human_RBP_ID_8709922,Human_RBP_ID_8931488,Human_RBP_ID_9241293,Human_RBP_ID_10486067,Human_RBP_ID_16771523,Human_RBP_ID_17057648,Human_RBP_ID_17065902,Human_RBP_ID_17177723,Human_RBP_ID_17202892,Human_RBP_ID_17324101,Human_RBP_ID_17439457,Human_RBP_ID_17551551,Human_RBP_ID_18142336,Human_RBP_ID_18203943,Human_RBP_ID_18212995,Human_RBP_ID_18521826,Human_RBP_ID_18542828,Human_RBP_ID_18912893,Human_RBP_ID_21763627,Human_RBP_ID_21957191,Human_RBP_ID_22342733,Human_RBP_ID_22412345,Human_RBP_ID_22839920,Human_RBP_ID_23096253,Human_RBP_ID_23202043,Human_RBP_ID_23301095,Human_RBP_ID_23317186,Human_RBP_ID_24318254,Human_RBP_ID_24393770,Human_RBP_ID_26245610,Human_RBP_ID_26567473,Human_RBP_ID_26740635,Human_RBP_ID_26752719,Human_RBP_ID_27140416,Human_RBP_ID_27163095,Human_RBP_ID_27377647,Human_RBP_ID_27548542,Human_RBP_ID_27788464 60144 RMVar_ID_60144 Human_SNP_ID_737723863 m1A Human chrM + 9066 9066 9066 CTCATGCACCTAATTGGAAGCGCCACCCTAGCAATATCAACCATTAACCTTCCCTCTACACTTAT CTCATGCACCTAATTGGAAGCGCCACCCTAGCGATATCAACCATTAACCTTCCCTCTACACTTAT A G MT-ATP6 Ensembl:ENSG00000198899 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrMT:8901..9413 26863196 MeRIP-seq:(Medium) rs1556423601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287490,Human_RBP_ID_723496,Human_RBP_ID_798913,Human_RBP_ID_1120201,Human_RBP_ID_1228686,Human_RBP_ID_1404343,Human_RBP_ID_1708972,Human_RBP_ID_2067732,Human_RBP_ID_3233691,Human_RBP_ID_3911966,Human_RBP_ID_5431658,Human_RBP_ID_5516843,Human_RBP_ID_7960091,Human_RBP_ID_8161399,Human_RBP_ID_8276765,Human_RBP_ID_8709931,Human_RBP_ID_9241438,Human_RBP_ID_10443649,Human_RBP_ID_16771555,Human_RBP_ID_17057649,Human_RBP_ID_17202900,Human_RBP_ID_17324106,Human_RBP_ID_17439462,Human_RBP_ID_17551562,Human_RBP_ID_17717250,Human_RBP_ID_18142342,Human_RBP_ID_18203949,Human_RBP_ID_18213004,Human_RBP_ID_18521836,Human_RBP_ID_18542915,Human_RBP_ID_18912898,Human_RBP_ID_21764485,Human_RBP_ID_21957192,Human_RBP_ID_22342737,Human_RBP_ID_22518796,Human_RBP_ID_22839934,Human_RBP_ID_23096270,Human_RBP_ID_23202053,Human_RBP_ID_23300969,Human_RBP_ID_24318269,Human_RBP_ID_24537867,Human_RBP_ID_26245626,Human_RBP_ID_26567482,Human_RBP_ID_26740643,Human_RBP_ID_26752724,Human_RBP_ID_27140424,Human_RBP_ID_27163211,Human_RBP_ID_27377656,Human_RBP_ID_27548551 60145 RMVar_ID_60145 Human_SNP_ID_737723866 m1A Human chrM + 9073 9073 9073 ACCTAATTGGAAGCGCCACCCTAGCAATATCAACCATTAACCTTCCCTCTACACTTATCATCTTC ACCTAATTGGAAGCGCCACCCTAGCAATATCAGCCATTAACCTTCCCTCTACACTTATCATCTTC A G MT-ATP6 Ensembl:ENSG00000198899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chrMT:8876..9666;chrMT:8923..10344;chrMT:8917..9977;chrMT:8901..9652;chrMT:8876..9375;chrMT:8876..9343;chrMT:8928..9645 26863196 MeRIP-seq:(Medium) rs1556423603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723496,Human_RBP_ID_798913,Human_RBP_ID_1120201,Human_RBP_ID_1228686,Human_RBP_ID_1404343,Human_RBP_ID_1708972,Human_RBP_ID_2067732,Human_RBP_ID_3233691,Human_RBP_ID_3911966,Human_RBP_ID_5431658,Human_RBP_ID_5516843,Human_RBP_ID_7960091,Human_RBP_ID_8161399,Human_RBP_ID_8276765,Human_RBP_ID_8709931,Human_RBP_ID_9241438,Human_RBP_ID_10443649,Human_RBP_ID_16771556,Human_RBP_ID_17057649,Human_RBP_ID_17202900,Human_RBP_ID_17324106,Human_RBP_ID_17439462,Human_RBP_ID_17551562,Human_RBP_ID_17717250,Human_RBP_ID_18142342,Human_RBP_ID_18203949,Human_RBP_ID_18213004,Human_RBP_ID_18521836,Human_RBP_ID_18542915,Human_RBP_ID_18912898,Human_RBP_ID_21764485,Human_RBP_ID_21957192,Human_RBP_ID_22342737,Human_RBP_ID_22518796,Human_RBP_ID_22839934,Human_RBP_ID_23096270,Human_RBP_ID_23202053,Human_RBP_ID_23300969,Human_RBP_ID_24318269,Human_RBP_ID_24537867,Human_RBP_ID_26245626,Human_RBP_ID_26567482,Human_RBP_ID_26740643,Human_RBP_ID_26752724,Human_RBP_ID_27140424,Human_RBP_ID_27163211,Human_RBP_ID_27377656,Human_RBP_ID_27548551 60146 RMVar_ID_60146 Human_SNP_ID_737723978 m1A Human chrM + 9531 9531 9531 TCTGAGCCTTTTACCACTCCAGCCTAGCCCCTACCCCCCAATTAGGAGGGCACTGGCCCCCAACA TCTGAGCCTTTTACCACTCCAGCCTAGCCCCTGCCCCCCAATTAGGAGGGCACTGGCCCCCAACA A G MT-CO3 Ensembl:ENSG00000198938 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrMT:9451..9625 32194978 MeRIP-seq:(Medium) rs386829082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723511,Human_RBP_ID_798916,Human_RBP_ID_1120205,Human_RBP_ID_1228705,Human_RBP_ID_1404355,Human_RBP_ID_2067743,Human_RBP_ID_3911977,Human_RBP_ID_5244389,Human_RBP_ID_5516852,Human_RBP_ID_7960129,Human_RBP_ID_8239543,Human_RBP_ID_8276777,Human_RBP_ID_8709952,Human_RBP_ID_9241303,Human_RBP_ID_10486073,Human_RBP_ID_16771631,Human_RBP_ID_17065915,Human_RBP_ID_17177733,Human_RBP_ID_17202912,Human_RBP_ID_17324112,Human_RBP_ID_17551586,Human_RBP_ID_18186009,Human_RBP_ID_18203953,Human_RBP_ID_18213013,Human_RBP_ID_18521851,Human_RBP_ID_18912909,Human_RBP_ID_22412353,Human_RBP_ID_22839954,Human_RBP_ID_23096770,Human_RBP_ID_23317196,Human_RBP_ID_24524765,Human_RBP_ID_26567766,Human_RBP_ID_26740652,Human_RBP_ID_26752731,Human_RBP_ID_27163120,Human_RBP_ID_27548564 60147 RMVar_ID_60147 Human_SNP_ID_737724036 m1A Human chrM - 9836 9836 9836 CGGATGAAGCAGATAGTGAGGAAAGTTGAGCCAATAATGACGTGAAGTCCGTGGAAGCCTGTGGC CGGATGAAGCAGATAGTGAGGAAAGTTGAGCCGATAATGACGTGAAGTCCGTGGAAGCCTGTGGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrMT:9744..9897 26863196 MeRIP-seq:(Medium) rs1556423731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1228713,Human_RBP_ID_1709001,Human_RBP_ID_2067750,Human_RBP_ID_3233980,Human_RBP_ID_5230469,Human_RBP_ID_7960143,Human_RBP_ID_8276781,Human_RBP_ID_8709966,Human_RBP_ID_8931517,Human_RBP_ID_10443671,Human_RBP_ID_16771658,Human_RBP_ID_18142355,Human_RBP_ID_18521857,Human_RBP_ID_22839963,Human_RBP_ID_23096319,Human_RBP_ID_23142135,Human_RBP_ID_23317316,Human_RBP_ID_24318326,Human_RBP_ID_26740656,Human_RBP_ID_27140453,Human_RBP_ID_27163134,Human_RBP_ID_27548580,Human_RBP_ID_27570892,Human_RBP_ID_27788473 60148 RMVar_ID_60148 Human_SNP_ID_737724091 m1A Human chrM + 10133 10133 10133 TTACTACTAATAATTATTACATTTTGACTACCACAACTCAACGGCTACATAGAAAAATCCACCCC TTACTACTAATAATTATTACATTTTGACTACCCCAACTCAACGGCTACATAGAAAAATCCACCCC A C MT-ND3 Ensembl:ENSG00000198840 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrMT:10126..10356 26863410 MeRIP-seq:(Medium) rs28409867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271373,Human_RBP_ID_287330,Human_RBP_ID_723057,Human_RBP_ID_1228219,Human_RBP_ID_1404010,Human_RBP_ID_1708411,Human_RBP_ID_2067440,Human_RBP_ID_3232975,Human_RBP_ID_3911663,Human_RBP_ID_5230510,Human_RBP_ID_7959052,Human_RBP_ID_8161197,Human_RBP_ID_8276342,Human_RBP_ID_8709369,Human_RBP_ID_8931018,Human_RBP_ID_9240995,Human_RBP_ID_16770051,Human_RBP_ID_17202503,Human_RBP_ID_17439173,Human_RBP_ID_17550872,Human_RBP_ID_18141855,Human_RBP_ID_18212485,Human_RBP_ID_18521484,Human_RBP_ID_18542483,Human_RBP_ID_18912545,Human_RBP_ID_21763473,Human_RBP_ID_21957270,Human_RBP_ID_22119985,Human_RBP_ID_22342456,Human_RBP_ID_22518612,Human_RBP_ID_22839192,Human_RBP_ID_23095510,Human_RBP_ID_26245737,Human_RBP_ID_26566904,Human_RBP_ID_26740374,Human_RBP_ID_27140073,Human_RBP_ID_27162595,Human_RBP_ID_27547946 60149 RMVar_ID_60149 Human_SNP_ID_737724100 m1A Human chrM - 10166 10166 10166 GCGGGGGATATAGGGTCGAAGCCGCACTCGTAAGGGGTGGATTTTTCTATGTAGCCGTTGAGTTG GCGGGGGATATAGGGTCGAAGCCGCACTCGTAGGGGGTGGATTTTTCTATGTAGCCGTTGAGTTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrMT:10116..10303 26863196 MeRIP-seq:(Medium) rs1556423772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1228221,Human_RBP_ID_3232985,Human_RBP_ID_3911668,Human_RBP_ID_7959051,Human_RBP_ID_8276345,Human_RBP_ID_8709374,Human_RBP_ID_8931025,Human_RBP_ID_10443171,Human_RBP_ID_16770045,Human_RBP_ID_17065697,Human_RBP_ID_17202919,Human_RBP_ID_17439174,Human_RBP_ID_18521487,Human_RBP_ID_18542485,Human_RBP_ID_21763474,Human_RBP_ID_22518614,Human_RBP_ID_22839200,Human_RBP_ID_23095501,Human_RBP_ID_23201617,Human_RBP_ID_27788240 60150 RMVar_ID_60150 Human_SNP_ID_737724161 m1A Human chrM + 10499 10499 10499 CAAATGCCCCTCATTTACATAAATATTATACTAGCATTTACCATCTCACTTCTAGGAATACTAGT CAAATGCCCCTCATTTACATAAATATTATACTGGCATTTACCATCTCACTTCTAGGAATACTAGT A G MT-ND4L Ensembl:ENSG00000212907 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrMT:10426..10500 26863196 MeRIP-seq:(Medium) rs1057520074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287333,Human_RBP_ID_723065,Human_RBP_ID_1228234,Human_RBP_ID_1404021,Human_RBP_ID_1708434,Human_RBP_ID_2067453,Human_RBP_ID_3233005,Human_RBP_ID_3911676,Human_RBP_ID_5044230,Human_RBP_ID_5482652,Human_RBP_ID_5516610,Human_RBP_ID_7959096,Human_RBP_ID_8161207,Human_RBP_ID_8276359,Human_RBP_ID_8709390,Human_RBP_ID_8931040,Human_RBP_ID_9241003,Human_RBP_ID_16770095,Human_RBP_ID_17057407,Human_RBP_ID_17065701,Human_RBP_ID_17177624,Human_RBP_ID_17202513,Human_RBP_ID_17323824,Human_RBP_ID_17439183,Human_RBP_ID_17550889,Human_RBP_ID_17717096,Human_RBP_ID_18141870,Human_RBP_ID_18212494,Human_RBP_ID_18521500,Human_RBP_ID_18542489,Human_RBP_ID_18912557,Human_RBP_ID_21764491,Human_RBP_ID_22119992,Human_RBP_ID_22342468,Human_RBP_ID_22424939,Human_RBP_ID_22518621,Human_RBP_ID_22839220,Human_RBP_ID_23095533,Human_RBP_ID_23201632,Human_RBP_ID_23300884,Human_RBP_ID_24317469,Human_RBP_ID_26244858,Human_RBP_ID_26566924,Human_RBP_ID_26740380,Human_RBP_ID_27140084,Human_RBP_ID_27162614,Human_RBP_ID_27377319,Human_RBP_ID_27547968,Human_RBP_ID_27788253 60151 RMVar_ID_60151 Human_SNP_ID_737724163 m1A Human chrM + 10514 10514 10514 TACATAAATATTATACTAGCATTTACCATCTCACTTCTAGGAATACTAGTATATCGCTCACACCT TACATAAATATTATACTAGCATTTACCATCTCGCTTCTAGGAATACTAGTATATCGCTCACACCT A G MT-ND4L Ensembl:ENSG00000212907 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrMT:10501..12099 26863410 MeRIP-seq:(Medium) rs386829102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723065,Human_RBP_ID_1228235,Human_RBP_ID_1404021,Human_RBP_ID_1708434,Human_RBP_ID_2067454,Human_RBP_ID_3233006,Human_RBP_ID_3911677,Human_RBP_ID_5431506,Human_RBP_ID_5516611,Human_RBP_ID_7959096,Human_RBP_ID_8161207,Human_RBP_ID_8276359,Human_RBP_ID_8709391,Human_RBP_ID_8931040,Human_RBP_ID_9241004,Human_RBP_ID_17057407,Human_RBP_ID_17202514,Human_RBP_ID_17323824,Human_RBP_ID_17439183,Human_RBP_ID_17550889,Human_RBP_ID_17717096,Human_RBP_ID_18141870,Human_RBP_ID_18203579,Human_RBP_ID_18212495,Human_RBP_ID_18542491,Human_RBP_ID_22424939,Human_RBP_ID_23095533,Human_RBP_ID_23300884,Human_RBP_ID_24317469,Human_RBP_ID_26244858,Human_RBP_ID_26566924,Human_RBP_ID_27162614,Human_RBP_ID_27547968,Human_RBP_ID_27788253 60152 RMVar_ID_60152 Human_SNP_ID_737724466 m1A Human chrM - 12175 12175 12175 CGGTAAATAAGGGGTCGTAAGCCTCTGTTGTCAGATTCACAATCTGATGTTTTGGTTAAACTATA CGGTAAATAAGGGGTCGTAAGCCTCTGTTGTCGGATTCACAATCTGATGTTTTGGTTAAACTATA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrMT:12126..12200 26863196 MeRIP-seq:(Medium) rs1057520099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1708511,Human_RBP_ID_7959263,Human_RBP_ID_8276421,Human_RBP_ID_8709482,Human_RBP_ID_16770323,Human_RBP_ID_17717113,Human_RBP_ID_18203642,Human_RBP_ID_18212568,Human_RBP_ID_18521536,Human_RBP_ID_18912600,Human_RBP_ID_23095671,Human_RBP_ID_24317583 Clinvar_Rec_208 60153 RMVar_ID_60153 Human_SNP_ID_737724756 m1A Human chrM + 13710 13710 13710 CCCACCCTACTAAACCCCATTAAACGCCTGGCAGCCGGAAGCCTATTCGCAGGATTTCTCATTAC CCCACCCTACTAAACCCCATTAAACGCCTGGCCGCCGGAAGCCTATTCGCAGGATTTCTCATTAC A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs200295632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271249,Human_RBP_ID_1228390,Human_RBP_ID_1708613,Human_RBP_ID_3233816,Human_RBP_ID_5482669,Human_RBP_ID_7959404,Human_RBP_ID_8276488,Human_RBP_ID_8709589,Human_RBP_ID_8931179,Human_RBP_ID_10443355,Human_RBP_ID_16770519,Human_RBP_ID_17057482,Human_RBP_ID_17065769,Human_RBP_ID_17202630,Human_RBP_ID_18213139,Human_RBP_ID_18521586,Human_RBP_ID_22518673,Human_RBP_ID_22839458,Human_RBP_ID_23095806,Human_RBP_ID_23141949,Human_RBP_ID_23317048,Human_RBP_ID_24317693,Human_RBP_ID_26567072,Human_RBP_ID_26740461,Human_RBP_ID_27788326 60154 RMVar_ID_60154 Human_SNP_ID_737724757 m1A Human chrM + 13710 13710 13710 CCCACCCTACTAAACCCCATTAAACGCCTGGCAGCCGGAAGCCTATTCGCAGGATTTCTCATTAC CCCACCCTACTAAACCCCATTAAACGCCTGGCGGCCGGAAGCCTATTCGCAGGATTTCTCATTAC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs200295632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271249,Human_RBP_ID_1228390,Human_RBP_ID_1708613,Human_RBP_ID_3233816,Human_RBP_ID_5482669,Human_RBP_ID_7959404,Human_RBP_ID_8276488,Human_RBP_ID_8709589,Human_RBP_ID_8931179,Human_RBP_ID_10443355,Human_RBP_ID_16770519,Human_RBP_ID_17057482,Human_RBP_ID_17065769,Human_RBP_ID_17202630,Human_RBP_ID_18213139,Human_RBP_ID_18521586,Human_RBP_ID_22518673,Human_RBP_ID_22839458,Human_RBP_ID_23095806,Human_RBP_ID_23141949,Human_RBP_ID_23317048,Human_RBP_ID_24317693,Human_RBP_ID_26567072,Human_RBP_ID_26740461,Human_RBP_ID_27788326 60155 RMVar_ID_60155 Human_SNP_ID_737724957 m1A Human chrM + 14596 14596 14596 ACACCGCTAACAATCAATACTAAACCCCCATAAATAGGAGAAGGCTTAGAAGAAAACCCCACAAA ACACCGCTAACAATCAATACTAAACCCCCATATATAGGAGAAGGCTTAGAAGAAAACCCCACAAA A T - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs387906424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24317758 Clinvar_Rec_209 GWAS_ID_7262 60156 RMVar_ID_60156 Human_SNP_ID_737724958 m1A Human chrM + 14597 14597 14597 CACCGCTAACAATCAATACTAAACCCCCATAAATAGGAGAAGGCTTAGAAGAAAACCCCACAAAC CACCGCTAACAATCAATACTAAACCCCCATAAGTAGGAGAAGGCTTAGAAGAAAACCCCACAAAC A G MT-ND6 Ensembl:ENSG00000198695 Protein coding CDS GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs797045055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16770636,Human_RBP_ID_24317757 Clinvar_Rec_210 60157 RMVar_ID_60157 Human_SNP_ID_737724993 m1A Human chrM + 14793 14793 14793 CAAAACTAACCCCCTAATAAAATTAATTAACCACTCATTCATCGACCTCCCCACCCCATCCAACA CAAAACTAACCCCCTAATAAAATTAATTAACCGCTCATTCATCGACCTCCCCACCCCATCCAACA A G MT-CYB Ensembl:ENSG00000198727 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2853504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1120134,Human_RBP_ID_1708674,Human_RBP_ID_2067579,Human_RBP_ID_3233353,Human_RBP_ID_3911797,Human_RBP_ID_5244566,Human_RBP_ID_8709642,Human_RBP_ID_8931222,Human_RBP_ID_9241393,Human_RBP_ID_9355244,Human_RBP_ID_10443402,Human_RBP_ID_16770662,Human_RBP_ID_17065791,Human_RBP_ID_17177673,Human_RBP_ID_17202672,Human_RBP_ID_17323941,Human_RBP_ID_17439315,Human_RBP_ID_18203726,Human_RBP_ID_18521616,Human_RBP_ID_18542671,Human_RBP_ID_21763530,Human_RBP_ID_21957317,Human_RBP_ID_22412363,Human_RBP_ID_22839550,Human_RBP_ID_23095895,Human_RBP_ID_23317085,Human_RBP_ID_24317774,Human_RBP_ID_26245220,Human_RBP_ID_26567125,Human_RBP_ID_26752529,Human_RBP_ID_27548209 60158 RMVar_ID_60158 Human_SNP_ID_737725143 m1A Human chrM - 15454 15454 15454 GGTGAGAATAGTGTTAATGTCATTAAGGAGAGAAGGAAGAGAAGTAAGCCGAGGGCGTCTTTGAT GGTGAGAATAGTGTTAATGTCATTAAGGAGAGGAGGAAGAGAAGTAAGCCGAGGGCGTCTTTGAT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrMT:15253..15808 26863410 MeRIP-seq:(Medium) rs879015290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3233397,Human_RBP_ID_7959550,Human_RBP_ID_8709673,Human_RBP_ID_16770744,Human_RBP_ID_17203009,Human_RBP_ID_18212731,Human_RBP_ID_18521637,Human_RBP_ID_21764055,Human_RBP_ID_22839582,Human_RBP_ID_23095935,Human_RBP_ID_23201861,Human_RBP_ID_27788362 Human_miRNA_ID_3119341,Human_miRNA_ID_3119342 60159 RMVar_ID_60159 Human_SNP_ID_737725145 m1A Human chrM - 15458 15458 15458 GTCTGGTGAGAATAGTGTTAATGTCATTAAGGAGAGAAGGAAGAGAAGTAAGCCGAGGGCGTCTT GTCTGGTGAGAATAGTGTTAATGTCATTAAGGGGAGAAGGAAGAGAAGTAAGCCGAGGGCGTCTT T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrMT:15284..15638 26863410 MeRIP-seq:(Medium) rs527236185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3233397,Human_RBP_ID_5044663,Human_RBP_ID_7959550,Human_RBP_ID_8709673,Human_RBP_ID_10486031,Human_RBP_ID_16770744,Human_RBP_ID_17065807,Human_RBP_ID_17070636,Human_RBP_ID_17203009,Human_RBP_ID_18212731,Human_RBP_ID_18521637,Human_RBP_ID_21764055,Human_RBP_ID_22839582,Human_RBP_ID_23095935,Human_RBP_ID_23201861,Human_RBP_ID_26567162,Human_RBP_ID_27788362 Human_miRNA_ID_3119341,Human_miRNA_ID_3119342 Clinvar_Rec_211 60160 RMVar_ID_60160 Human_SNP_ID_737725274 m1A Human chrM - 15942 15942 15942 TTAAAGACTTTTTCTCTGATTTGTCCTTGGAAAAAGGTTTTCATCTCCGGTTTACAAGACTGGTG TTAAAGACTTTTTCTCTGATTTGTCCTTGGAAGAAGGTTTTCATCTCCGGTTTACAAGACTGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrMT:15901..15950 26863196 MeRIP-seq:(Medium) rs28535186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271282,Human_RBP_ID_1228482,Human_RBP_ID_1404170,Human_RBP_ID_1708738,Human_RBP_ID_2067603,Human_RBP_ID_3233436,Human_RBP_ID_3911835,Human_RBP_ID_5230559,Human_RBP_ID_5277744,Human_RBP_ID_5431566,Human_RBP_ID_5454861,Human_RBP_ID_5516714,Human_RBP_ID_7959607,Human_RBP_ID_8276570,Human_RBP_ID_8709698,Human_RBP_ID_8931278,Human_RBP_ID_9241136,Human_RBP_ID_10443451,Human_RBP_ID_16770812,Human_RBP_ID_17057538,Human_RBP_ID_17065819,Human_RBP_ID_17177682,Human_RBP_ID_17202731,Human_RBP_ID_17717157,Human_RBP_ID_18142155,Human_RBP_ID_18203774,Human_RBP_ID_18213194,Human_RBP_ID_18521653,Human_RBP_ID_18912717,Human_RBP_ID_21764556,Human_RBP_ID_21907330,Human_RBP_ID_21957166,Human_RBP_ID_22412288,Human_RBP_ID_22424955,Human_RBP_ID_22839624,Human_RBP_ID_23096588,Human_RBP_ID_23142002,Human_RBP_ID_23300937,Human_RBP_ID_24317847,Human_RBP_ID_24443838,Human_RBP_ID_24524683,Human_RBP_ID_24537857,Human_RBP_ID_26245315,Human_RBP_ID_26567183,Human_RBP_ID_26740519,Human_RBP_ID_26752827,Human_RBP_ID_27140256,Human_RBP_ID_27162859,Human_RBP_ID_27377478,Human_RBP_ID_27548268,Human_RBP_ID_27788371 60161 RMVar_ID_60161 Human_SNP_ID_737725287 m1A Human chrM - 15970 15970 15970 ATCTTAGCTTTGGGTGCTAATGGTGGAGTTAAAGACTTTTTCTCTGATTTGTCCTTGGAAAAAGG ATCTTAGCTTTGGGTGCTAATGGTGGAGTTAAGGACTTTTTCTCTGATTTGTCCTTGGAAAAAGG T C MT-TP Ensembl:ENSG00000210196 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs375213730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271282,Human_RBP_ID_723271,Human_RBP_ID_798943,Human_RBP_ID_847903,Human_RBP_ID_966186,Human_RBP_ID_1120138,Human_RBP_ID_1146865,Human_RBP_ID_1228482,Human_RBP_ID_1340236,Human_RBP_ID_1404171,Human_RBP_ID_1708738,Human_RBP_ID_2067606,Human_RBP_ID_3233436,Human_RBP_ID_3911835,Human_RBP_ID_5045073,Human_RBP_ID_5091122,Human_RBP_ID_5155136,Human_RBP_ID_5230503,Human_RBP_ID_5271801,Human_RBP_ID_5277745,Human_RBP_ID_5310223,Human_RBP_ID_5410749,Human_RBP_ID_5431567,Human_RBP_ID_5454862,Human_RBP_ID_5482680,Human_RBP_ID_5516715,Human_RBP_ID_5637261,Human_RBP_ID_5641221,Human_RBP_ID_5659256,Human_RBP_ID_7959608,Human_RBP_ID_8161304,Human_RBP_ID_8226379,Human_RBP_ID_8239566,Human_RBP_ID_8276570,Human_RBP_ID_8709698,Human_RBP_ID_8731529,Human_RBP_ID_8931278,Human_RBP_ID_9241137,Human_RBP_ID_9264867,Human_RBP_ID_9315987,Human_RBP_ID_9341865,Human_RBP_ID_9352077,Human_RBP_ID_9443080,Human_RBP_ID_10443452,Human_RBP_ID_10486104,Human_RBP_ID_16770813,Human_RBP_ID_17057539,Human_RBP_ID_17065820,Human_RBP_ID_17095698,Human_RBP_ID_17177683,Human_RBP_ID_17202959,Human_RBP_ID_17210619,Human_RBP_ID_17323976,Human_RBP_ID_17439343,Human_RBP_ID_17551231,Human_RBP_ID_17579851,Human_RBP_ID_17586443,Human_RBP_ID_17644585,Human_RBP_ID_17672625,Human_RBP_ID_17717158,Human_RBP_ID_18142155,Human_RBP_ID_18173720,Human_RBP_ID_18185952,Human_RBP_ID_18203774,Human_RBP_ID_18212760,Human_RBP_ID_18400813,Human_RBP_ID_18414648,Human_RBP_ID_18453848,Human_RBP_ID_18468185,Human_RBP_ID_18508111,Human_RBP_ID_18521653,Human_RBP_ID_18542893,Human_RBP_ID_18545094,Human_RBP_ID_18545798,Human_RBP_ID_18912717,Human_RBP_ID_18963335,Human_RBP_ID_19148116,Human_RBP_ID_21764446,Human_RBP_ID_21907330,Human_RBP_ID_21957166,Human_RBP_ID_21997201,Human_RBP_ID_22120095,Human_RBP_ID_22342614,Human_RBP_ID_22368868,Human_RBP_ID_22372699,Human_RBP_ID_22412288,Human_RBP_ID_22424955,Human_RBP_ID_22425324,Human_RBP_ID_22467485,Human_RBP_ID_22484887,Human_RBP_ID_22518709,Human_RBP_ID_22530937,Human_RBP_ID_22531870,Human_RBP_ID_22556926,Human_RBP_ID_22692269,Human_RBP_ID_22706385,Human_RBP_ID_22734117,Human_RBP_ID_22748487,Human_RBP_ID_22777509,Human_RBP_ID_22839624,Human_RBP_ID_23096340,Human_RBP_ID_23117359,Human_RBP_ID_23120961,Human_RBP_ID_23142002,Human_RBP_ID_23201885,Human_RBP_ID_23300938,Human_RBP_ID_24317851,Human_RBP_ID_24443886,Human_RBP_ID_24524683,Human_RBP_ID_24537857,Human_RBP_ID_24539379,Human_RBP_ID_24540792,Human_RBP_ID_24549882,Human_RBP_ID_24555677,Human_RBP_ID_24563800,Human_RBP_ID_26245316,Human_RBP_ID_26567183,Human_RBP_ID_26740519,Human_RBP_ID_26752558,Human_RBP_ID_26772755,Human_RBP_ID_26796944,Human_RBP_ID_27140256,Human_RBP_ID_27162859,Human_RBP_ID_27377479,Human_RBP_ID_27548268,Human_RBP_ID_27570823,Human_RBP_ID_27574942,Human_RBP_ID_27788376 60162 RMVar_ID_60162 Human_SNP_ID_737725348 m1A Human chrM + 16170 16169 16171 AATACTTGACCACCTGTAGTACATAAAAACCCAATCCACATCAAAACCCCCTCCCCATGCTTACA AATACTTGACCACCTGTAGTACATAAAAACCCTATCCACATCAAAACCCCCTCCCCATGCTTACA CAA TAG - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs386828864 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_1708756,Human_RBP_ID_3911840,Human_RBP_ID_7959628,Human_RBP_ID_8709712,Human_RBP_ID_17202736 60163 RMVar_ID_60163 Human_SNP_ID_737725351 m1A Human chrM + 16170 16170 16170 AATACTTGACCACCTGTAGTACATAAAAACCCAATCCACATCAAAACCCCCTCCCCATGCTTACA AATACTTGACCACCTGTAGTACATAAAAACCCGATCCACATCAAAACCCCCTCCCCATGCTTACA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs879121566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1708756,Human_RBP_ID_3911840,Human_RBP_ID_7959628,Human_RBP_ID_8709712,Human_RBP_ID_17202736 60164 RMVar_ID_60164 Human_SNP_ID_737725357 m1A Human chrM + 16177 16177 16177 GACCACCTGTAGTACATAAAAACCCAATCCACATCAAAACCCCCTCCCCATGCTTACAAGCAAGT GACCACCTGTAGTACATAAAAACCCAATCCACGTCAAAACCCCCTCCCCATGCTTACAAGCAAGT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1556424782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1708756,Human_RBP_ID_3911840,Human_RBP_ID_7959628,Human_RBP_ID_17202736 60165 RMVar_ID_60165 Human_SNP_ID_737725503 m1A Human chrM - 16362 16362 16362 GGACCCCTATCTGAGGGGGGTCATCCATGGGGACGAGAAGGGATTTGACTGTAATGTGCTATGTA GGACCCCTATCTGAGGGGGGTCATCCATGGGGGCGAGAAGGGATTTGACTGTAATGTGCTATGTA T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62581341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723286,Human_RBP_ID_1708761,Human_RBP_ID_2067613,Human_RBP_ID_3911842,Human_RBP_ID_7959637,Human_RBP_ID_8709718,Human_RBP_ID_16770851,Human_RBP_ID_17202743,Human_RBP_ID_21763546,Human_RBP_ID_22839642,Human_RBP_ID_23142010,Human_RBP_ID_23317124,Human_RBP_ID_24317866,Human_RBP_ID_27140268 60166 RMVar_ID_60166 Human_SNP_ID_737725528 m1A Human chrM + 16497 16497 16497 CACTTGGGGGTAGCTAAAGTGAACTGTATCCGACATCTGGTTCCTACTTCAGGGTCATAAAGCCT CACTTGGGGGTAGCTAAAGTGAACTGTATCCGGCATCTGGTTCCTACTTCAGGGTCATAAAGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrMT:16043..16551 26863196 MeRIP-seq:(Medium) rs376846509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26567208 60167 RMVar_ID_60167 Human_SNP_ID_618465745 m1A Human chr17 + 15250282 15250282 15250282 CATTCCTCCCTCATCACTGGCTGTTCATCCCCAGTCTCCTCTCCTTCCTGTACCCTCGTTAACCC CATTCCTCCCTCATCACTGGCTGTTCATCCCCTGTCTCCTCTCCTTCCTGTACCCTCGTTAACCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15250278..15250399 26863196 MeRIP-seq:(Medium) rs1445354066 Functional Loss SNV dbSNP153 33..33 33 - - - 60168 RMVar_ID_60168 Human_SNP_ID_618466449 m1A Human chr17 + 15253754 15253754 15253754 CCCAGCGATCTTGCACTTGACGGTCCTTCTGTATGGAACCTCCCCGAGATGTTCATATGGCTGGC CCCAGCGATCTTGCACTTGACGGTCCTTCTGTTTGGAACCTCCCCGAGATGTTCATATGGCTGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15253752..15253866 26863196 MeRIP-seq:(Medium) rs990850486 Functional Loss SNV dbSNP153 33..33 33 - - - 60169 RMVar_ID_60169 Human_SNP_ID_618468111 m1A Human chr17 - 15260759 15260759 15260759 TCGGCCTCACGCCCAGCGCTCTCCTCGCAGGCAGAAACTCCGCTGAGCAGAACTTGCCGCCAGAA TCGGCCTCACGCCCAGCGCTCTCCTCGCAGGCGGAAACTCCGCTGAGCAGAACTTGCCGCCAGAA T C PMP22 Ensembl:ENSG00000109099 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:15260715..15260792 26863196 MeRIP-seq:(Medium) rs1282340665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1781828,Human_Splice_Rec_1781836,Human_Splice_Rec_1781844,Human_Splice_Rec_1781860,Human_Splice_Rec_1781874,Human_Splice_Rec_1781890,Human_Splice_Rec_1781898,Human_Splice_Rec_1781906 RMVar_hsa_circ_329908,RMVar_hsa_circ_182207 60170 RMVar_ID_60170 Human_SNP_ID_618516352 m1A Human chr17 - 15464650 15464650 15464650 GTTTGAAAGCAGAAGGGGAAGGGTGCATAAGGAGGGACATTTGGAAAAGTGCTGGAGAGGGGAGC GTTTGAAAGCAGAAGGGGAAGGGTGCATAAGGGGGGACATTTGGAAAAGTGCTGGAGAGGGGAGC T C TVP23C-CDRT4,CDRT4 Ensembl:ENSG00000259024,Ensembl:ENSG00000239704 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15464601..15464735 26863196 MeRIP-seq:(Medium) rs376284433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648802 60171 RMVar_ID_60171 Human_SNP_ID_618516508 m1A Human chr17 + 15465097 15465094 15465098 CAGACACACACCAATACAGACACACACAACACAGACACACACCAACACACAGACACACCAACACA CAGACACACACCAATACAGACACACACAAC____ACACACACCAACACACAGACACACCAACACA CACAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15464958..15465733 26863196 MeRIP-seq:(Medium) rs1394323834 Functional Loss DEL dbSNP153 31..34 33 - - - 60172 RMVar_ID_60172 Human_SNP_ID_618516510 m1A Human chr17 + 15465097 15465096 15465098 CAGACACACACCAATACAGACACACACAACACAGACACACACCAACACACAGACACACCAACACA CAGACACACACCAATACAGACACACACAACAC__ACACACACCAACACACAGACACACCAACACA CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15464958..15465733 26863196 MeRIP-seq:(Medium) rs1451308806 Functional Loss DEL dbSNP153 33..34 33 - - - 60173 RMVar_ID_60173 Human_SNP_ID_618517195 m1A Human chr17 - 15467491 15467491 15467491 AACGCCGGGCAGGGGAACAGCCAAGATAGTGCAGGAAGGATGGGGAATCACAGAAACTTCTCAGG AACGCCGGGCAGGGGAACAGCCAAGATAGTGCGGGAAGGATGGGGAATCACAGAAACTTCTCAGG T C TVP23C-CDRT4,CDRT4 Ensembl:ENSG00000259024,Ensembl:ENSG00000239704 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15467470..15467605 26863196 MeRIP-seq:(Medium) rs1418535555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648423,Human_RBP_ID_23712005 Human_Splice_Rec_1781997 60174 RMVar_ID_60174 Human_SNP_ID_618522082 m1A Human chr17 + 15487721 15487717 15487722 CTATGACATATGTCACTACTTTACCTCTCTCAAGTCATCATCCAAACATCACCCTGTCACTTGCC CTATGACATATGTCACTACTTTACCTCTC_____TCATCATCCAAACATCACCCTGTCACTTGCC CTCAAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15487519..15487794 26863196 MeRIP-seq:(Medium) rs1238214134 Functional Loss DEL dbSNP153 30..34 33 - - - 60175 RMVar_ID_60175 Human_SNP_ID_618526275 m1A Human chr17 - 15502701 15502701 15502701 AAAGAGAGAGAGAGGAGAGAGAGAAAGAACGAACGAACAGGGAACTTGTAAAACTAAGGGGAAAA AAAGAGAGAGAGAGGAGAGAGAGAAAGAACGAGCGAACAGGGAACTTGTAAAACTAAGGGGAAAA T C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:15502617..15502871 26863196 MeRIP-seq:(Medium) rs886454372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6217,Human_RBP_ID_17653759 60176 RMVar_ID_60176 Human_SNP_ID_618526279 m1A Human chr17 - 15502709 15502707 15502709 GGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGAAAGAACGAACGAACAGGGAACTTGTAAAACTAA GGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA__GAACGAACGAACAGGGAACTTGTAAAACTAA CTT C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:15502662..15502828 26863196 MeRIP-seq:(Medium) rs1416394815 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6217,Human_RBP_ID_17068086,Human_RBP_ID_25337886 60177 RMVar_ID_60177 Human_SNP_ID_618526282 m1A Human chr17 - 15502709 15502709 15502709 GGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGAAAGAACGAACGAACAGGGAACTTGTAAAACTAA GGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGAGAGAACGAACGAACAGGGAACTTGTAAAACTAA T C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:15502662..15502828 26863196 MeRIP-seq:(Medium) rs116291298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6217,Human_RBP_ID_17068086,Human_RBP_ID_25337886 60178 RMVar_ID_60178 Human_SNP_ID_618526308 m1A Human chr17 - 15502742 15502736 15502742 GTGACGGAGAAGGAGAGAAAGAGACGGGAGAGAGGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA GTGACGGAGAAGGAGAGAAAGAGACGGGAGAG______GAGAAAGAGAGAGAGAGGAGAGAGAGA CTCTCCT C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:15502560..15502901;chr17:15502640..15502917 26863196 MeRIP-seq:(Medium) rs1433283491 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_9845916,Human_RBP_ID_17068086,Human_RBP_ID_17207060,Human_RBP_ID_25250520 60179 RMVar_ID_60179 Human_SNP_ID_618526312 m1A Human chr17 - 15502742 15502740 15502742 GTGACGGAGAAGGAGAGAAAGAGACGGGAGAGAGGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA GTGACGGAGAAGGAGAGAAAGAGACGGGAGAG__GAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA CCT C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:15502560..15502901;chr17:15502640..15502917 26863196 MeRIP-seq:(Medium) rs1341735564 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9845916,Human_RBP_ID_17068086,Human_RBP_ID_17207060,Human_RBP_ID_25250520 60180 RMVar_ID_60180 Human_SNP_ID_618526314 m1A Human chr17 - 15502742 15502742 15502742 GTGACGGAGAAGGAGAGAAAGAGACGGGAGAGAGGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA GTGACGGAGAAGGAGAGAAAGAGACGGGAGAGGGGAGAGAGAAAGAGAGAGAGAGGAGAGAGAGA T C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:15502560..15502901;chr17:15502640..15502917 26863196 MeRIP-seq:(Medium) rs79839249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9845916,Human_RBP_ID_17068086,Human_RBP_ID_17207060,Human_RBP_ID_25250520 60181 RMVar_ID_60181 Human_SNP_ID_618529779 m1A Human chr17 + 15516523 15516523 15516523 TTGTGGACGGCATCTTCCCCCTTCGTCTTCACACGGTCCTTCCTCTGTGTGTCTGTGTCCTAATA TTGTGGACGGCATCTTCCCCCTTCGTCTTCACGCGGTCCTTCCTCTGTGTGTCTGTGTCCTAATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:15516474..15516598 26863196 MeRIP-seq:(Medium) rs892676733 Functional Loss SNV dbSNP153 33..33 33 - - - 60182 RMVar_ID_60182 Human_SNP_ID_618540569 m1A Human chr17 + 15563495 15563495 15563495 AGCCCTGCTTCCAGGAGCCACGTCAGCGCAGCAGCGTACGGGTCCGGGTCGGAACTGACGCGACC AGCCCTGCTTCCAGGAGCCACGTCAGCGCAGCCGCGTACGGGTCCGGGTCGGAACTGACGCGACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:15563370..15563494 26863196 MeRIP-seq:(Medium) rs1039718842 Functional Loss SNV dbSNP153 33..33 33 - - - 60183 RMVar_ID_60183 Human_SNP_ID_618540571 m1A Human chr17 + 15563500 15563500 15563500 TGCTTCCAGGAGCCACGTCAGCGCAGCAGCGTACGGGTCCGGGTCGGAACTGACGCGACCCGTCA TGCTTCCAGGAGCCACGTCAGCGCAGCAGCGTGCGGGTCCGGGTCGGAACTGACGCGACCCGTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15563369..15563505 26863196 MeRIP-seq:(Medium) rs1412619912 Functional Loss SNV dbSNP153 33..33 33 - - - 60184 RMVar_ID_60184 Human_SNP_ID_618540572 m1A Human chr17 + 15563500 15563500 15563500 TGCTTCCAGGAGCCACGTCAGCGCAGCAGCGTACGGGTCCGGGTCGGAACTGACGCGACCCGTCA TGCTTCCAGGAGCCACGTCAGCGCAGCAGCGTTCGGGTCCGGGTCGGAACTGACGCGACCCGTCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15563369..15563505 26863196 MeRIP-seq:(Medium) rs1412619912 Functional Loss SNV dbSNP153 33..33 33 - - - 60185 RMVar_ID_60185 Human_SNP_ID_618563225 m1A Human chr17 - 15656473 15656473 15656473 GAGGACTCCCATCCACCTAGGCATAGGAAATGAGAGAAGGAGCTACACGGGTTGAGAGGTGGCAG GAGGACTCCCATCCACCTAGGCATAGGAAATGGGAGAAGGAGCTACACGGGTTGAGAGGTGGCAG T C TRIM16 Ensembl:ENSG00000221926 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:15656423..15656679 26863196 MeRIP-seq:(Medium) rs1291664198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6561520,Human_RBP_ID_8189369 60186 RMVar_ID_60186 Human_SNP_ID_618566025 m1A Human chr17 - 15668638 15668638 15668638 TGGTGTGTTTTCATGTGCAAAAGTGTGTTTTCATGTGCAAAAGCCTAGAGACAGGAGAAAACGGC TGGTGTGTTTTCATGTGCAAAAGTGTGTTTTCGTGTGCAAAAGCCTAGAGACAGGAGAAAACGGC T C TRIM16 Ensembl:ENSG00000221926 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15668564..15668641 26863196 MeRIP-seq:(Medium) rs1480579657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6561606,Human_RBP_ID_23712170 RMVar_hsa_circ_303372,RMVar_hsa_circ_325632 60187 RMVar_ID_60187 Human_SNP_ID_618566026 m1A Human chr17 - 15668638 15668638 15668638 TGGTGTGTTTTCATGTGCAAAAGTGTGTTTTCATGTGCAAAAGCCTAGAGACAGGAGAAAACGGC TGGTGTGTTTTCATGTGCAAAAGTGTGTTTTCCTGTGCAAAAGCCTAGAGACAGGAGAAAACGGC T G TRIM16 Ensembl:ENSG00000221926 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15668564..15668641 26863196 MeRIP-seq:(Medium) rs1480579657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6561606,Human_RBP_ID_23712170 RMVar_hsa_circ_303372,RMVar_hsa_circ_325632 60188 RMVar_ID_60188 Human_SNP_ID_618573568 m1A Human chr17 - 15699779 15699774 15699779 GCCGAGACGAGCGACATCACCACAAGCAACTCACCTCCCATCCCGGGCCTCACAAAGGGGACGAA GCCGAGACGAGCGACATCACCACAAGCAACTC_____CCATCCCGGGCCTCACAAAGGGGACGAA GGAGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:15699769..15699861;chr17:15699772..15699867;chr17:15699768..15699861 26863196 MeRIP-seq:(Medium) rs1336976183 Functional Loss DEL dbSNP153 33..37 33 - - - 60189 RMVar_ID_60189 Human_SNP_ID_618573575 m1A Human chr17 - 15699788 15699788 15699788 CGAGGCCGAGCCGAGACGAGCGACATCACCACAAGCAACTCACCTCCCATCCCGGGCCTCACAAA CGAGGCCGAGCCGAGACGAGCGACATCACCACGAGCAACTCACCTCCCATCCCGGGCCTCACAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:15699781..15699852 26863196 MeRIP-seq:(Medium) rs1308773053 Functional Loss SNV dbSNP153 33..33 33 - - - 60190 RMVar_ID_60190 Human_SNP_ID_618595831 m1A Human chr17 - 15786495 15786495 15786495 GGGGTGGGCAGGAGGCCAGACGCGCGCCCCCCAACCCCCGCCGCCGTCAGCCGCAGGCGCCGGGC GGGGTGGGCAGGAGGCCAGACGCGCGCCCCCCCACCCCCGCCGCCGTCAGCCGCAGGCGCCGGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15786385..15786568 26863196 MeRIP-seq:(Medium) rs1469720555 Functional Loss SNV dbSNP153 33..33 33 - - - 60191 RMVar_ID_60191 Human_SNP_ID_618634569 m1A Human chr17 + 15945249 15945249 15945249 TAGGGGGCGCCCGGGGCCCAGCTGGCCCGGCCATGCTGCTGGAGACACAGGACGCGCTGTACGTG TAGGGGGCGCCCGGGGCCCAGCTGGCCCGGCCGTGCTGCTGGAGACACAGGACGCGCTGTACGTG A G ADORA2B Ensembl:ENSG00000170425 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:15945161..15945358 26863410 MeRIP-seq:(Medium) rs1486709273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466106 60192 RMVar_ID_60192 Human_SNP_ID_618634628 m1A Human chr17 + 15945364 15945364 15945364 GTGCGCCGCGGTGGGCACGGCGAACACTCTGCAGACGCCCACCAACTACTTCCTGGTGTCCCTGG GTGCGCCGCGGTGGGCACGGCGAACACTCTGCGGACGCCCACCAACTACTTCCTGGTGTCCCTGG A G ADORA2B Ensembl:ENSG00000170425 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15945313..15945435 26863196 MeRIP-seq:(Medium) rs766104812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465174,Human_RBP_ID_5419814,Human_RBP_ID_5441127,Human_RBP_ID_5498178 60193 RMVar_ID_60193 Human_SNP_ID_618640438 m1A Human chr17 - 15967020 15967020 15967020 TCTGCCTCCCTCCCTGTGCTCCGAACACCCTCAGGTCTGCATGCGTTTGTCCATCTCCCCAAAAC TCTGCCTCCCTCCCTGTGCTCCGAACACCCTCGGGTCTGCATGCGTTTGTCCATCTCCCCAAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:15967013..15967096 26863196 MeRIP-seq:(Medium) rs923703840 Functional Loss SNV dbSNP153 33..33 33 - - - 60194 RMVar_ID_60194 Human_SNP_ID_618649295 m1A Human chr17 - 15999563 15999563 15999563 GATGGCCGTAGTGTTGCCGGCGGTTGTGGAGGAGCTCCTGAGCGAGATGGCGGCGGCGGTGCAGG GATGGCCGTAGTGTTGCCGGCGGTTGTGGAGGCGCTCCTGAGCGAGATGGCGGCGGCGGTGCAGG T G ZSWIM7 Ensembl:ENSG00000214941 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:15993798..15999668;chr17:15993798..15999636;chr17:15999494..15999661 26863196 MeRIP-seq:(Medium) rs771804863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465176 Human_Splice_Rec_1782901,Human_Splice_Rec_1782911,Human_Splice_Rec_1782933,Human_Splice_Rec_1782961,Human_Splice_Rec_1782969,Human_Splice_Rec_1782977,Human_Splice_Rec_1782987,Human_Splice_Rec_1782997,Human_Splice_Rec_1783007,Human_Splice_Rec_1783025,Human_Splice_Rec_1783039,Human_Splice_Rec_1783049,Human_Splice_Rec_1783063 60195 RMVar_ID_60195 Human_SNP_ID_618649723 m1A Human chr17 + 16000202 16000202 16000202 AGCCGACGGGGCCGCTGCCGAGGACGGGGCGGACGAGGCCGAGGCAGAGATCATCCAGCTGCTGA AGCCGACGGGGCCGCTGCCGAGGACGGGGCGGGCGAGGCCGAGGCAGAGATCATCCAGCTGCTGA A G TTC19 Ensembl:ENSG00000011295 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:15999727..16000374 26863196 MeRIP-seq:(Medium) rs1567575308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820047,Human_RBP_ID_899442,Human_RBP_ID_3950127,Human_RBP_ID_4407144,Human_RBP_ID_9377602,Human_RBP_ID_12897810,Human_RBP_ID_18987949,Human_RBP_ID_22959766 Human_Splice_Rec_1783072,Human_Splice_Rec_1783082,Human_Splice_Rec_1783100,Human_Splice_Rec_1783101,Human_Splice_Rec_1783120,Human_Splice_Rec_1783121,Human_Splice_Rec_1783138,Human_Splice_Rec_1783139 RMVar_hsa_circ_11866,RMVar_hsa_circ_23724 60196 RMVar_ID_60196 Human_SNP_ID_618649726 m1A Human chr17 + 16000205 16000205 16000205 CGACGGGGCCGCTGCCGAGGACGGGGCGGACGAGGCCGAGGCAGAGATCATCCAGCTGCTGAAGC CGACGGGGCCGCTGCCGAGGACGGGGCGGACGGGGCCGAGGCAGAGATCATCCAGCTGCTGAAGC A G TTC19 Ensembl:ENSG00000011295 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:16000078..16000250;chr17:15999805..16000338;chr17:15999799..16000348 26863196 MeRIP-seq:(Medium) rs979048292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820047,Human_RBP_ID_899442,Human_RBP_ID_3950127,Human_RBP_ID_4407144,Human_RBP_ID_5363766,Human_RBP_ID_9377602,Human_RBP_ID_12897810,Human_RBP_ID_18987949,Human_RBP_ID_22959766 Human_Splice_Rec_1783072,Human_Splice_Rec_1783082,Human_Splice_Rec_1783100,Human_Splice_Rec_1783101,Human_Splice_Rec_1783120,Human_Splice_Rec_1783121,Human_Splice_Rec_1783138,Human_Splice_Rec_1783139 RMVar_hsa_circ_11866,RMVar_hsa_circ_23724 60197 RMVar_ID_60197 Human_SNP_ID_618650171 m1A Human chr17 - 16001859 16001859 16001859 AGAAAATGAAACATATAGTAGATGCATATGCTAAGAGACAGAAGTGTATGCAACTGTACATCCCA AGAAAATGAAACATATAGTAGATGCATATGCTGAGAGACAGAAGTGTATGCAACTGTACATCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16001856..16001946 26863196 MeRIP-seq:(Medium) rs181443630 Functional Loss SNV dbSNP153 33..33 33 - - - 60198 RMVar_ID_60198 Human_SNP_ID_618665589 m1A Human chr17 - 16061836 16061836 16061836 TAAGCCAAGGCCTGCCAGCCTCCCGTTACAACACTGCTGCGGATGCCCTGGCTGCTCTTGTGGAT TAAGCCAAGGCCTGCCAGCCTCCCGTTACAACGCTGCTGCGGATGCCCTGGCTGCTCTTGTGGAT T C NCOR1 Ensembl:ENSG00000141027 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:16061785..16062146 32194978 MeRIP-seq:(Medium) rs1189570304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4468366,Human_RBP_ID_6562551,Human_RBP_ID_8813459,Human_RBP_ID_9289851,Human_RBP_ID_18689788,Human_RBP_ID_27813449 Human_Splice_Rec_1783228,Human_Splice_Rec_1783312,Human_Splice_Rec_1783354,Human_Splice_Rec_1783442,Human_Splice_Rec_1783443,Human_Splice_Rec_1783478,Human_Splice_Rec_1783550,Human_Splice_Rec_1783570 Human_miRNA_ID_2696107 RMVar_hsa_circ_14121,RMVar_hsa_circ_32572,RMVar_hsa_circ_265016,RMVar_hsa_circ_42083,RMVar_hsa_circ_41091,RMVar_hsa_circ_20950,RMVar_hsa_circ_123107,RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_348241,RMVar_hsa_circ_60155,RMVar_hsa_circ_73233,RMVar_hsa_circ_38408,RMVar_hsa_circ_182248,RMVar_hsa_circ_182247,RMVar_hsa_circ_18892,RMVar_hsa_circ_101359,RMVar_hsa_circ_366355,RMVar_hsa_circ_372745,RMVar_hsa_circ_376449,RMVar_hsa_circ_371096,RMVar_hsa_circ_365893,RMVar_hsa_circ_336814,RMVar_hsa_circ_340342,RMVar_hsa_circ_182249,RMVar_hsa_circ_182250,RMVar_hsa_circ_29564,RMVar_hsa_circ_182254,RMVar_hsa_circ_94048,RMVar_hsa_circ_301205,RMVar_hsa_circ_320447,RMVar_hsa_circ_182255,RMVar_hsa_circ_182253 60199 RMVar_ID_60199 Human_SNP_ID_618671762 m1A Human chr17 + 16086415 16086415 16086415 TCGGAAGCCGAACGCCTTCAGGGAGATTAGTTATCACTTGATGTGGAGCAGGCTGAAGGACTTTT TCGGAAGCCGAACGCCTTCAGGGAGATTAGTTGTCACTTGATGTGGAGCAGGCTGAAGGACTTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:16086311..16087290 32194978 MeRIP-seq:(Medium) rs1339026901 Functional Loss SNV dbSNP153 33..33 33 - - - 60200 RMVar_ID_60200 Human_SNP_ID_618676067 m1A Human chr17 + 16101516 16101516 16101516 GCTTTGGTAGCGGGTGGGGGATCACAAACAGAACCCTCTTCAGCACTGTGCTCCTGCTGATCTAC GCTTTGGTAGCGGGTGGGGGATCACAAACAGAGCCCTCTTCAGCACTGTGCTCCTGCTGATCTAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:16101465..16101566 32194978 MeRIP-seq:(Medium) rs757380085 Functional Loss SNV dbSNP153 33..33 33 - - - 60201 RMVar_ID_60201 Human_SNP_ID_618681209 m1A Human chr17 + 16121221 16121221 16121221 CGCCCCCGGGGTGTGGCTTGCTCTCTTTCCTCAGTTTCTTCTGCTGTACCATCTATCTTGTCCTT CGCCCCCGGGGTGTGGCTTGCTCTCTTTCCTCGGTTTCTTCTGCTGTACCATCTATCTTGTCCTT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:16121176..16121225 26863196 MeRIP-seq:(Medium) rs779267917 Functional Loss SNV dbSNP153 33..33 33 - - - 60202 RMVar_ID_60202 Human_SNP_ID_618681214 m1A Human chr17 - 16121252 16121252 16121252 TGCTTTTGTGTCCAGAGAAAATACCAAGGAAAAGGACAAGATAGATGGTACAGCAGAAGAAACTG TGCTTTTGTGTCCAGAGAAAATACCAAGGAAAGGGACAAGATAGATGGTACAGCAGAAGAAACTG T C NCOR1 Ensembl:ENSG00000141027 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16121087..16121315 26863196 MeRIP-seq:(Medium) rs1342819834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6716,Human_RBP_ID_48342,Human_RBP_ID_201538,Human_RBP_ID_899456,Human_RBP_ID_1546633,Human_RBP_ID_1849688,Human_RBP_ID_2494904,Human_RBP_ID_3951866,Human_RBP_ID_5467361,Human_RBP_ID_9346160,Human_RBP_ID_9375432,Human_RBP_ID_18411999,Human_RBP_ID_18469991,Human_RBP_ID_18987961,Human_RBP_ID_22959168,Human_RBP_ID_24544794,Human_RBP_ID_24552250,Human_RBP_ID_26331331,Human_RBP_ID_27812337 Human_Splice_Rec_1783186,Human_Splice_Rec_1783272,Human_Splice_Rec_1783400,Human_Splice_Rec_1783598,Human_Splice_Rec_1783612 Human_miRNA_ID_2255451,Human_miRNA_ID_2255452 RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_348241,RMVar_hsa_circ_372745,RMVar_hsa_circ_182249,RMVar_hsa_circ_182257,RMVar_hsa_circ_116302,RMVar_hsa_circ_98921,RMVar_hsa_circ_108863,RMVar_hsa_circ_123782,RMVar_hsa_circ_182260,RMVar_hsa_circ_182261,RMVar_hsa_circ_107798,RMVar_hsa_circ_182262,RMVar_hsa_circ_182263,RMVar_hsa_circ_96187,RMVar_hsa_circ_182270,RMVar_hsa_circ_16539,RMVar_hsa_circ_27721,RMVar_hsa_circ_72882,RMVar_hsa_circ_85654,RMVar_hsa_circ_60427,RMVar_hsa_circ_182275,RMVar_hsa_circ_357715,RMVar_hsa_circ_110802,RMVar_hsa_circ_23603,RMVar_hsa_circ_17899,RMVar_hsa_circ_55959,RMVar_hsa_circ_126613,RMVar_hsa_circ_182278,RMVar_hsa_circ_182277,RMVar_hsa_circ_375567,RMVar_hsa_circ_31076,RMVar_hsa_circ_119362,RMVar_hsa_circ_182283,RMVar_hsa_circ_182284,RMVar_hsa_circ_182282,RMVar_hsa_circ_67688,RMVar_hsa_circ_40412,RMVar_hsa_circ_659,RMVar_hsa_circ_48508,RMVar_hsa_circ_353205,RMVar_hsa_circ_354871,RMVar_hsa_circ_366029,RMVar_hsa_circ_282921,RMVar_hsa_circ_63783,RMVar_hsa_circ_75424,RMVar_hsa_circ_44380,RMVar_hsa_circ_264849,RMVar_hsa_circ_182288,RMVar_hsa_circ_23465,RMVar_hsa_circ_182289,RMVar_hsa_circ_341336,RMVar_hsa_circ_353936,RMVar_hsa_circ_319903,RMVar_hsa_circ_64286,RMVar_hsa_circ_66074,RMVar_hsa_circ_56158,RMVar_hsa_circ_358851 60203 RMVar_ID_60203 Human_SNP_ID_618682390 m1A Human chr17 - 16126134 16126125 16126134 AAGAAGAGGATAAAGCAGAAAAAACAGAAAAAAAAGAAGAAGAAAAGAAAGATGAAGAGGAAAAA AAGAAGAGGATAAAGCAGAAAAAACAGAAAAA_________GAAAAGAAAGATGAAGAGGAAAAA CTTCTTCTTT C NCOR1 Ensembl:ENSG00000141027 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16126019..16126225 26863196 MeRIP-seq:(Medium) rs1158483508 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_48343,Human_RBP_ID_200424,Human_RBP_ID_899458,Human_RBP_ID_1238451,Human_RBP_ID_1546634,Human_RBP_ID_9345967,Human_RBP_ID_18990571,Human_RBP_ID_24544985,Human_RBP_ID_25252157 Human_Splice_Rec_1783184,Human_Splice_Rec_1783185,Human_Splice_Rec_1783270,Human_Splice_Rec_1783271,Human_Splice_Rec_1783398,Human_Splice_Rec_1783399,Human_Splice_Rec_1783596,Human_Splice_Rec_1783597,Human_Splice_Rec_1783648,Human_Splice_Rec_1783678,Human_Splice_Rec_1783708,Human_Splice_Rec_1783736 RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_348241,RMVar_hsa_circ_372745,RMVar_hsa_circ_182249,RMVar_hsa_circ_182257,RMVar_hsa_circ_116302,RMVar_hsa_circ_98921,RMVar_hsa_circ_108863,RMVar_hsa_circ_123782,RMVar_hsa_circ_182260,RMVar_hsa_circ_182261,RMVar_hsa_circ_107798,RMVar_hsa_circ_182262,RMVar_hsa_circ_182263,RMVar_hsa_circ_96187,RMVar_hsa_circ_182270,RMVar_hsa_circ_16539,RMVar_hsa_circ_27721,RMVar_hsa_circ_72882,RMVar_hsa_circ_85654,RMVar_hsa_circ_60427,RMVar_hsa_circ_182275,RMVar_hsa_circ_357715,RMVar_hsa_circ_110802,RMVar_hsa_circ_23603,RMVar_hsa_circ_17899,RMVar_hsa_circ_55959,RMVar_hsa_circ_126613,RMVar_hsa_circ_182278,RMVar_hsa_circ_182277,RMVar_hsa_circ_375567,RMVar_hsa_circ_119362,RMVar_hsa_circ_182283,RMVar_hsa_circ_182284,RMVar_hsa_circ_182282,RMVar_hsa_circ_67688,RMVar_hsa_circ_40412,RMVar_hsa_circ_659,RMVar_hsa_circ_48508,RMVar_hsa_circ_353205,RMVar_hsa_circ_354871,RMVar_hsa_circ_282921,RMVar_hsa_circ_63783,RMVar_hsa_circ_75424,RMVar_hsa_circ_44380,RMVar_hsa_circ_264849,RMVar_hsa_circ_182288,RMVar_hsa_circ_23465,RMVar_hsa_circ_182289,RMVar_hsa_circ_341336,RMVar_hsa_circ_353936,RMVar_hsa_circ_64286,RMVar_hsa_circ_66074,RMVar_hsa_circ_56158,RMVar_hsa_circ_48922,RMVar_hsa_circ_288975,RMVar_hsa_circ_378569,RMVar_hsa_circ_353375,RMVar_hsa_circ_61405,RMVar_hsa_circ_182290 60204 RMVar_ID_60204 Human_SNP_ID_618682393 m1A Human chr17 - 16126134 16126131 16126134 AAGAAGAGGATAAAGCAGAAAAAACAGAAAAAAAAGAAGAAGAAAAGAAAGATGAAGAGGAAAAA AAGAAGAGGATAAAGCAGAAAAAACAGAAAAA___GAAGAAGAAAAGAAAGATGAAGAGGAAAAA CTTT C NCOR1 Ensembl:ENSG00000141027 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16126019..16126225 26863196 MeRIP-seq:(Medium) rs759535259 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_48343,Human_RBP_ID_200424,Human_RBP_ID_899458,Human_RBP_ID_1238451,Human_RBP_ID_1546634,Human_RBP_ID_9345967,Human_RBP_ID_18990571,Human_RBP_ID_24544985,Human_RBP_ID_25252157 Human_Splice_Rec_1783184,Human_Splice_Rec_1783185,Human_Splice_Rec_1783270,Human_Splice_Rec_1783271,Human_Splice_Rec_1783398,Human_Splice_Rec_1783399,Human_Splice_Rec_1783596,Human_Splice_Rec_1783597,Human_Splice_Rec_1783648,Human_Splice_Rec_1783678,Human_Splice_Rec_1783708,Human_Splice_Rec_1783736 RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_348241,RMVar_hsa_circ_372745,RMVar_hsa_circ_182249,RMVar_hsa_circ_182257,RMVar_hsa_circ_116302,RMVar_hsa_circ_98921,RMVar_hsa_circ_108863,RMVar_hsa_circ_123782,RMVar_hsa_circ_182260,RMVar_hsa_circ_182261,RMVar_hsa_circ_107798,RMVar_hsa_circ_182262,RMVar_hsa_circ_182263,RMVar_hsa_circ_96187,RMVar_hsa_circ_182270,RMVar_hsa_circ_16539,RMVar_hsa_circ_27721,RMVar_hsa_circ_72882,RMVar_hsa_circ_85654,RMVar_hsa_circ_60427,RMVar_hsa_circ_182275,RMVar_hsa_circ_357715,RMVar_hsa_circ_110802,RMVar_hsa_circ_23603,RMVar_hsa_circ_17899,RMVar_hsa_circ_55959,RMVar_hsa_circ_126613,RMVar_hsa_circ_182278,RMVar_hsa_circ_182277,RMVar_hsa_circ_375567,RMVar_hsa_circ_119362,RMVar_hsa_circ_182283,RMVar_hsa_circ_182284,RMVar_hsa_circ_182282,RMVar_hsa_circ_67688,RMVar_hsa_circ_40412,RMVar_hsa_circ_659,RMVar_hsa_circ_48508,RMVar_hsa_circ_353205,RMVar_hsa_circ_354871,RMVar_hsa_circ_282921,RMVar_hsa_circ_63783,RMVar_hsa_circ_75424,RMVar_hsa_circ_44380,RMVar_hsa_circ_264849,RMVar_hsa_circ_182288,RMVar_hsa_circ_23465,RMVar_hsa_circ_182289,RMVar_hsa_circ_341336,RMVar_hsa_circ_353936,RMVar_hsa_circ_64286,RMVar_hsa_circ_66074,RMVar_hsa_circ_56158,RMVar_hsa_circ_48922,RMVar_hsa_circ_288975,RMVar_hsa_circ_378569,RMVar_hsa_circ_353375,RMVar_hsa_circ_61405,RMVar_hsa_circ_182290 60205 RMVar_ID_60205 Human_SNP_ID_618707392 m1A Human chr17 + 16214862 16214862 16214862 TTTGCCATCTCCACCAGTACCCAGCCTTCGCCATTACACCCTGAAGCGGTCTGTTAGAAAGGTGA TTTGCCATCTCCACCAGTACCCAGCCTTCGCCGTTACACCCTGAAGCGGTCTGTTAGAAAGGTGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16214858..16215154 26863196 MeRIP-seq:(Medium) rs1345050175 Functional Loss SNV dbSNP153 33..33 33 - - - 60206 RMVar_ID_60206 Human_SNP_ID_618707616 m1A Human chr17 + 16215408 16215408 16215408 GCGTGGGAGCCGACGTGCGCCCCGGCCTGAGGAGTGGGACGCGGCCACGGCGCGCGGCCCTACAC GCGTGGGAGCCGACGTGCGCCCCGGCCTGAGGGGTGGGACGCGGCCACGGCGCGCGGCCCTACAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:16215351..16215525 26863196 MeRIP-seq:(Medium) rs1039572294 Functional Loss SNV dbSNP153 33..33 33 - - - 60207 RMVar_ID_60207 Human_SNP_ID_618707661 m1A Human chr17 - 16215501 16215501 16215501 AGTCAAGATGGCGGCCAAGGTGGCGAAGCAGCAGCCGCGGCGGCGGCGGCGGCTGGAGTGAGCGT AGTCAAGATGGCGGCCAAGGTGGCGAAGCAGCGGCCGCGGCGGCGGCGGCGGCTGGAGTGAGCGT T C NCOR1 Ensembl:ENSG00000141027 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:16215351..16215550;chr17:16215401..16215550;chr17:16215371..16215550 26863196 MeRIP-seq:(Medium) rs1413073305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237864,Human_RBP_ID_4407464,Human_RBP_ID_9375447,Human_RBP_ID_26331347 60208 RMVar_ID_60208 Human_SNP_ID_618707663 m1A Human chr17 - 16215504 16215504 16215504 TTGAGTCAAGATGGCGGCCAAGGTGGCGAAGCAGCAGCCGCGGCGGCGGCGGCGGCTGGAGTGAG TTGAGTCAAGATGGCGGCCAAGGTGGCGAAGCGGCAGCCGCGGCGGCGGCGGCGGCTGGAGTGAG T C NCOR1 Ensembl:ENSG00000141027 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16215398..16215524 26863196 MeRIP-seq:(Medium) rs1374939408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237864,Human_RBP_ID_4407464,Human_RBP_ID_9375447,Human_RBP_ID_26331347 60209 RMVar_ID_60209 Human_SNP_ID_618708426 m1A Human chr17 + 16217301 16217301 16217301 GCATGGGGCTTCCTCTGGGTTTGGGACTCCTCAGAACGAATGAAGAGTCGGGAGCAGGGAGGACG GCATGGGGCTTCCTCTGGGTTTGGGACTCCTCCGAACGAATGAAGAGTCGGGAGCAGGGAGGACG A C PIGL Ensembl:ENSG00000108474 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16217251..16217379 26863196 MeRIP-seq:(Medium) rs766413777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483703,Human_RBP_ID_1528388,Human_RBP_ID_3513384,Human_RBP_ID_5441133,Human_RBP_ID_9377641,Human_RBP_ID_22209364,Human_RBP_ID_23712800 60210 RMVar_ID_60210 Human_SNP_ID_618708461 m1A Human chr17 - 16217400 16217400 16217400 TGCCTTAGGCGGGCCAAGCCTAGCACTGTGGGAGCAAAAAACATGGCTTCATCGTCAGGGTGCGC TGCCTTAGGCGGGCCAAGCCTAGCACTGTGGGGGCAAAAAACATGGCTTCATCGTCAGGGTGCGC T C NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:16217351..16217400 32194978 MeRIP-seq:(Medium) rs752226508 Functional Loss SNV dbSNP153 33..33 33 - - - 60211 RMVar_ID_60211 Human_SNP_ID_618720731 m1A Human chr17 + 16267366 16267366 16267366 GGTGGCAGAGGCGGAAGAGGTGGAGGAAGTGGATGGGGAGGCGGAAGAGGTGGAGGAAGTGGATG GGTGGCAGAGGCGGAAGAGGTGGAGGAAGTGGGTGGGGAGGCGGAAGAGGTGGAGGAAGTGGATG A G PIGL Ensembl:ENSG00000108474 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16267341..16267458 26863196 MeRIP-seq:(Medium) rs1380457405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70177,RMVar_hsa_circ_66197 60212 RMVar_ID_60212 Human_SNP_ID_618733167 m1A Human chr17 + 16320307 16320307 16320307 GGGGAGGGGAGGGAGGGAGGAAGGGGAAGGGAAGGGAAGGAAGGAAGGGAAGCGAAGGAAGGAAG GGGGAGGGGAGGGAGGGAGGAAGGGGAAGGGACGGGAAGGAAGGAAGGGAAGCGAAGGAAGGAAG A C PIGL Ensembl:ENSG00000108474 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16320303..16320398 26863196 MeRIP-seq:(Medium) rs1265410910 Functional Loss SNV dbSNP153 33..33 33 - - - 60213 RMVar_ID_60213 Human_SNP_ID_618733181 m1A Human chr17 + 16320338 16320334 16320339 AAGGGAAGGAAGGAAGGGAAGCGAAGGAAGGAAGGGAAGGGAAGGAAGAAGGAAGGAAGAGAGAG AAGGGAAGGAAGGAAGGGAAGCGAAGGAA_____GGAAGGGAAGGAAGAAGGAAGGAAGAGAGAG AGGAAG A PIGL Ensembl:ENSG00000108474 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16320290..16320427 26863196 MeRIP-seq:(Medium) rs980455447 Functional Loss DEL dbSNP153 30..34 33 - - - 60214 RMVar_ID_60214 Human_SNP_ID_618741624 m1A Human chr17 - 16353154 16353136 16353154 CGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGACTCCCGCGACCCCGACGTCCTCGGCGTCCAAC CGTTGCTCCCGCCACCGCCGCCGCCGCCGCCG__________________TCCTCGGCGTCCAAC ACGTCGGGGTCGCGGGAGT A CENPV Ensembl:ENSG00000166582 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16353103..16353429 26863196 MeRIP-seq:(Medium) rs764124502 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_236564,Human_RBP_ID_4464347,Human_RBP_ID_5237867,Human_RBP_ID_22442816 RMVar_hsa_circ_126839,RMVar_hsa_circ_182319 60215 RMVar_ID_60215 Human_SNP_ID_618741632 m1A Human chr17 - 16353154 16353154 16353154 CGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGACTCCCGCGACCCCGACGTCCTCGGCGTCCAAC CGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGCCTCCCGCGACCCCGACGTCCTCGGCGTCCAAC T G CENPV Ensembl:ENSG00000166582 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16353103..16353429 26863196 MeRIP-seq:(Medium) rs776175621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236564,Human_RBP_ID_4464347,Human_RBP_ID_5237867,Human_RBP_ID_22442816 RMVar_hsa_circ_126839,RMVar_hsa_circ_182319 60216 RMVar_ID_60216 Human_SNP_ID_618741649 m1A Human chr17 - 16353173 16353164 16353173 CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGACTCCCGCGACCCC CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCC_________GCCGCCGCCGACTCCCGCGACCCC CGGCGGCGGT C CENPV Ensembl:ENSG00000166582 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16353126..16353475 26863196 MeRIP-seq:(Medium) rs746979329 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_236564,Human_RBP_ID_4407566,Human_RBP_ID_5237867,Human_RBP_ID_22442816 RMVar_hsa_circ_126839,RMVar_hsa_circ_182319 60217 RMVar_ID_60217 Human_SNP_ID_618741655 m1A Human chr17 - 16353173 16353173 16353173 CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGACTCCCGCGACCCC CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCCGCCGCCGCCGCCGCCGCCGACTCCCGCGACCCC T C CENPV Ensembl:ENSG00000166582 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16353126..16353475 26863196 MeRIP-seq:(Medium) rs768145241 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_236564,Human_RBP_ID_4407566,Human_RBP_ID_5237867,Human_RBP_ID_22442816 RMVar_hsa_circ_126839,RMVar_hsa_circ_182319 60218 RMVar_ID_60218 Human_SNP_ID_618741747 m1A Human chr17 + 16353358 16353358 16353358 GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGAGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGCGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:16353080..16353450;chr17:16353076..16353450 26863410 MeRIP-seq:(Medium) rs754483275 Functional Loss SNV dbSNP153 33..33 33 - - - 60219 RMVar_ID_60219 Human_SNP_ID_618741748 m1A Human chr17 + 16353358 16353358 16353358 GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGAGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGGGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:16353080..16353450;chr17:16353076..16353450 26863410 MeRIP-seq:(Medium) rs754483275 Functional Loss SNV dbSNP153 33..33 33 - - - 60220 RMVar_ID_60220 Human_SNP_ID_618748981 m1A Human chr17 - 16381150 16381150 16381150 GTTAGCGGATACCAGGATCCTGCCAATCACCAACCACGTCCACCCACAGGGACACAAACAAGCTC GTTAGCGGATACCAGGATCCTGCCAATCACCAGCCACGTCCACCCACAGGGACACAAACAAGCTC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:16381101..16381278;chr17:16381101..16381200;chr17:16381101..16381175 26863196 MeRIP-seq:(Medium) rs1376418481 Functional Loss SNV dbSNP153 33..33 33 - - - 60221 RMVar_ID_60221 Human_SNP_ID_618748982 m1A Human chr17 - 16381150 16381150 16381150 GTTAGCGGATACCAGGATCCTGCCAATCACCAACCACGTCCACCCACAGGGACACAAACAAGCTC GTTAGCGGATACCAGGATCCTGCCAATCACCACCCACGTCCACCCACAGGGACACAAACAAGCTC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:16381101..16381278;chr17:16381101..16381200;chr17:16381101..16381175 26863196 MeRIP-seq:(Medium) rs1376418481 Functional Loss SNV dbSNP153 33..33 33 - - - 60222 RMVar_ID_60222 Human_SNP_ID_618748989 m1A Human chr17 + 16381165 16381165 16381165 CCTGTGGGTGGACGTGGTTGGTGATTGGCAGGATCCTGGTATCCGCTAACAGGTACTGGCCCGCA CCTGTGGGTGGACGTGGTTGGTGATTGGCAGGCTCCTGGTATCCGCTAACAGGTACTGGCCCGCA A C UBB Ensembl:ENSG00000170315 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:16381076..16381345 26863196 MeRIP-seq:(Medium) rs1487869507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236708,Human_RBP_ID_277948,Human_RBP_ID_483785,Human_RBP_ID_766074,Human_RBP_ID_820455,Human_RBP_ID_1006397,Human_RBP_ID_1180268,Human_RBP_ID_1284562,Human_RBP_ID_1528429,Human_RBP_ID_1849799,Human_RBP_ID_3513451,Human_RBP_ID_4465181,Human_RBP_ID_5184387,Human_RBP_ID_5318272,Human_RBP_ID_5419828,Human_RBP_ID_5441142,Human_RBP_ID_5466115,Human_RBP_ID_5496533,Human_RBP_ID_5526191,Human_RBP_ID_6563320,Human_RBP_ID_8088923,Human_RBP_ID_8445075,Human_RBP_ID_8813537,Human_RBP_ID_8941885,Human_RBP_ID_9069396,Human_RBP_ID_9326493,Human_RBP_ID_12902127,Human_RBP_ID_17691297,Human_RBP_ID_17885911,Human_RBP_ID_18420473,Human_RBP_ID_18689925,Human_RBP_ID_22442817,Human_RBP_ID_22498774,Human_RBP_ID_22947321,Human_RBP_ID_23128902,Human_RBP_ID_23209829,Human_RBP_ID_23712866,Human_RBP_ID_27662017 Human_Splice_Rec_1783889,Human_Splice_Rec_1783893,Human_Splice_Rec_1783895 RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322 60223 RMVar_ID_60223 Human_SNP_ID_618748990 m1A Human chr17 + 16381165 16381165 16381165 CCTGTGGGTGGACGTGGTTGGTGATTGGCAGGATCCTGGTATCCGCTAACAGGTACTGGCCCGCA CCTGTGGGTGGACGTGGTTGGTGATTGGCAGGTTCCTGGTATCCGCTAACAGGTACTGGCCCGCA A T UBB Ensembl:ENSG00000170315 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:16381076..16381345 26863196 MeRIP-seq:(Medium) rs1487869507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236708,Human_RBP_ID_277948,Human_RBP_ID_483785,Human_RBP_ID_766074,Human_RBP_ID_820455,Human_RBP_ID_1006397,Human_RBP_ID_1180268,Human_RBP_ID_1284562,Human_RBP_ID_1528429,Human_RBP_ID_1849799,Human_RBP_ID_3513451,Human_RBP_ID_4465181,Human_RBP_ID_5184387,Human_RBP_ID_5318272,Human_RBP_ID_5419828,Human_RBP_ID_5441142,Human_RBP_ID_5466115,Human_RBP_ID_5496533,Human_RBP_ID_5526191,Human_RBP_ID_6563320,Human_RBP_ID_8088923,Human_RBP_ID_8445075,Human_RBP_ID_8813537,Human_RBP_ID_8941885,Human_RBP_ID_9069396,Human_RBP_ID_9326493,Human_RBP_ID_12902127,Human_RBP_ID_17691297,Human_RBP_ID_17885911,Human_RBP_ID_18420473,Human_RBP_ID_18689925,Human_RBP_ID_22442817,Human_RBP_ID_22498774,Human_RBP_ID_22947321,Human_RBP_ID_23128902,Human_RBP_ID_23209829,Human_RBP_ID_23712866,Human_RBP_ID_27662017 Human_Splice_Rec_1783889,Human_Splice_Rec_1783893,Human_Splice_Rec_1783895 RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322 60224 RMVar_ID_60224 Human_SNP_ID_618748996 m1A Human chr17 - 16381179 16381179 16381179 AAGGTCGTTACGGCTGCGGGCCAGTACCTGTTAGCGGATACCAGGATCCTGCCAATCACCAACCA AAGGTCGTTACGGCTGCGGGCCAGTACCTGTTCGCGGATACCAGGATCCTGCCAATCACCAACCA T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:16381076..16381345 26863410 MeRIP-seq:(Medium) rs1398709146 Functional Loss SNV dbSNP153 33..33 33 - - - 60225 RMVar_ID_60225 Human_SNP_ID_618748997 m1A Human chr17 + 16381180 16381180 16381180 GGTTGGTGATTGGCAGGATCCTGGTATCCGCTAACAGGTACTGGCCCGCAGCCGTAACGACCTTG GGTTGGTGATTGGCAGGATCCTGGTATCCGCTCACAGGTACTGGCCCGCAGCCGTAACGACCTTG A C UBB Ensembl:ENSG00000170315 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,H2O2 treatment;HEK293T,untreat control chr17:16381076..16381225;chr17:16381076..16381230 26863410 MeRIP-seq:(Medium) rs1218546306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277948,Human_RBP_ID_483785,Human_RBP_ID_820455,Human_RBP_ID_1006397,Human_RBP_ID_1528429,Human_RBP_ID_4465182,Human_RBP_ID_5318272,Human_RBP_ID_5526191,Human_RBP_ID_8941885,Human_RBP_ID_9326493,Human_RBP_ID_18420473,Human_RBP_ID_22442817,Human_RBP_ID_22498774,Human_RBP_ID_23209831,Human_RBP_ID_23712866 Human_Splice_Rec_1783889,Human_Splice_Rec_1783893,Human_Splice_Rec_1783895 RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322 60226 RMVar_ID_60226 Human_SNP_ID_618748998 m1A Human chr17 + 16381180 16381180 16381180 GGTTGGTGATTGGCAGGATCCTGGTATCCGCTAACAGGTACTGGCCCGCAGCCGTAACGACCTTG GGTTGGTGATTGGCAGGATCCTGGTATCCGCTGACAGGTACTGGCCCGCAGCCGTAACGACCTTG A G UBB Ensembl:ENSG00000170315 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,H2O2 treatment;HEK293T,untreat control chr17:16381076..16381225;chr17:16381076..16381230 26863410 MeRIP-seq:(Medium) rs1218546306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277948,Human_RBP_ID_483785,Human_RBP_ID_820455,Human_RBP_ID_1006397,Human_RBP_ID_1528429,Human_RBP_ID_4465182,Human_RBP_ID_5318272,Human_RBP_ID_5526191,Human_RBP_ID_8941885,Human_RBP_ID_9326493,Human_RBP_ID_18420473,Human_RBP_ID_22442817,Human_RBP_ID_22498774,Human_RBP_ID_23209831,Human_RBP_ID_23712866 Human_Splice_Rec_1783889,Human_Splice_Rec_1783893,Human_Splice_Rec_1783895 RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322 60227 RMVar_ID_60227 Human_SNP_ID_618749318 m1A Human chr17 + 16381845 16381845 16381845 ATAGTTGCTAATTTTGAAGAATATTAGGTGTAAAAGCAAGAAATACAATGATCCTGAGGTGACAC ATAGTTGCTAATTTTGAAGAATATTAGGTGTATAAGCAAGAAATACAATGATCCTGAGGTGACAC A T UBB Ensembl:ENSG00000170315 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:16381836..16381966 26863410 MeRIP-seq:(Medium) rs1295215512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17609362 RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322 60228 RMVar_ID_60228 Human_SNP_ID_618749332 m1A Human chr17 - 16381872 16381872 16381872 GACCTAGTTTAAAAGTAAAACATAAGCGTGTCACCTCAGGATCATTGTATTTCTTGCTTTTACAC GACCTAGTTTAAAAGTAAAACATAAGCGTGTCGCCTCAGGATCATTGTATTTCTTGCTTTTACAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:16381870..16382104 26863196 MeRIP-seq:(Medium) rs1253803899 Functional Loss SNV dbSNP153 33..33 33 - - - 60229 RMVar_ID_60229 Human_SNP_ID_618749499 m1A Human chr17 + 16382234 16382234 16382234 ATCGAAAATGTGAAGGCCAAGATCCAGGATAAAGAAGGCATCCCTCCCGACCAGCAGAGGCTCAT ATCGAAAATGTGAAGGCCAAGATCCAGGATAAGGAAGGCATCCCTCCCGACCAGCAGAGGCTCAT A G UBB Ensembl:ENSG00000170315 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16382184..16382454 26863196 MeRIP-seq:(Medium) rs1060199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766080,Human_RBP_ID_1528440,Human_RBP_ID_1849805,Human_RBP_ID_3513457,Human_RBP_ID_4468454,Human_RBP_ID_5525373,Human_RBP_ID_6563332,Human_RBP_ID_8253188,Human_RBP_ID_8445082,Human_RBP_ID_9069402,Human_RBP_ID_12902142,Human_RBP_ID_18530464,Human_RBP_ID_18689929,Human_RBP_ID_22209453,Human_RBP_ID_22498776,Human_RBP_ID_22760714,Human_RBP_ID_22803203,Human_RBP_ID_23128903,Human_RBP_ID_24544801,Human_RBP_ID_26811957,Human_RBP_ID_26955121,Human_RBP_ID_27249980,Human_RBP_ID_27448780 Human_miRNA_ID_2870249 RMVar_hsa_circ_83428,RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322,RMVar_hsa_circ_119884,RMVar_hsa_circ_182323,RMVar_hsa_circ_182324 60230 RMVar_ID_60230 Human_SNP_ID_618749641 m1A Human chr17 - 16382615 16382615 16382615 AGTGCAGAGTAATGCCATCACTGGGCACTGCGAATGCCATGACTGAAGAATTAACAGCCACCCCT AGTGCAGAGTAATGCCATCACTGGGCACTGCGTATGCCATGACTGAAGAATTAACAGCCACCCCT T A AC093484.3 Ensembl:ENSG00000265401 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16382524..16382631 26863196 MeRIP-seq:(Medium) rs777603854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1783905 60231 RMVar_ID_60231 Human_SNP_ID_618762156 m1A Human chr17 + 16428339 16428339 16428339 TCCTCCGCAGCTGTGGTACTTCTGGCGGCGCCACGTGTTCATCTGGATCTCGTTCATAGACAGCT TCCTCCGCAGCTGTGGTACTTCTGGCGGCGCCGCGTGTTCATCTGGATCTCGTTCATAGACAGCT A G AC093484.1,TRPV2 Ensembl:ENSG00000239203,Ensembl:ENSG00000187688 lincRNA,Protein coding exon,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:16427521..16428386 32194978 MeRIP-seq:(Medium) rs1192568221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1783920,Human_Splice_Rec_1783921,Human_Splice_Rec_1783939,Human_Splice_Rec_1783943,Human_Splice_Rec_1783970 RMVar_hsa_circ_101752,RMVar_hsa_circ_372497,RMVar_hsa_circ_372150,RMVar_hsa_circ_107427,RMVar_hsa_circ_182328,RMVar_hsa_circ_182329,RMVar_hsa_circ_182327,RMVar_hsa_circ_182330,RMVar_hsa_circ_44664 60232 RMVar_ID_60232 Human_SNP_ID_618765476 m1A Human chr17 - 16439372 16439372 16439372 CGGGTTTGCACACCCCCACTGTGGGCCGGGGAACCGGGTCCCGGCCTTCGCAGACTCCAGGCTCT CGGGTTTGCACACCCCCACTGTGGGCCGGGGATCCGGGTCCCGGCCTTCGCAGACTCCAGGCTCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:16439326..16439400;chr17:16439051..16439455;chr17:16439276..16439650;chr17:16439326..16439466 26863196 MeRIP-seq:(Medium) rs1383780739 Functional Loss SNV dbSNP153 33..33 33 - - - 60233 RMVar_ID_60233 Human_SNP_ID_618765477 m1A Human chr17 - 16439373 16439373 16439373 TCGGGTTTGCACACCCCCACTGTGGGCCGGGGAACCGGGTCCCGGCCTTCGCAGACTCCAGGCTC TCGGGTTTGCACACCCCCACTGTGGGCCGGGGTACCGGGTCCCGGCCTTCGCAGACTCCAGGCTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16439326..16439751 26863196 MeRIP-seq:(Medium) rs35752829 Functional Loss SNV dbSNP153 33..33 33 - - - 60234 RMVar_ID_60234 Human_SNP_ID_618765579 m1A Human chr17 + 16439562 16439562 16439562 AGTGCCGTCAGAAGCGATAACTGACGACGTCTAATGTCTATCTGACCGCAGTCGCTGAAACCTCT AGTGCCGTCAGAAGCGATAACTGACGACGTCTGATGTCTATCTGACCGCAGTCGCTGAAACCTCT A G SNORD49B,SNHG29 Ensembl:ENSG00000277108,Ensembl:ENSG00000175061 snoRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16439558..16439651 26863196 MeRIP-seq:(Medium) rs1568932775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237291,Human_RBP_ID_269807,Human_RBP_ID_483842,Human_RBP_ID_768564,Human_RBP_ID_1006418,Human_RBP_ID_1091556,Human_RBP_ID_1284571,Human_RBP_ID_1528461,Human_RBP_ID_1849822,Human_RBP_ID_2495150,Human_RBP_ID_3513482,Human_RBP_ID_5184391,Human_RBP_ID_6563363,Human_RBP_ID_8253189,Human_RBP_ID_8445108,Human_RBP_ID_8813550,Human_RBP_ID_9069420,Human_RBP_ID_12902209,Human_RBP_ID_17258135,Human_RBP_ID_18207736,Human_RBP_ID_18689950,Human_RBP_ID_20291422,Human_RBP_ID_22655885,Human_RBP_ID_22740218,Human_RBP_ID_22947334,Human_RBP_ID_23712918,Human_RBP_ID_25252787,Human_RBP_ID_26955167,Human_RBP_ID_27250025 Human_Splice_Rec_1784006,Human_Splice_Rec_1784092,Human_Splice_Rec_1784150,Human_Splice_Rec_1784166,Human_Splice_Rec_1784210,Human_Splice_Rec_1784300,Human_Splice_Rec_1784314,Human_Splice_Rec_1784328,Human_Splice_Rec_1784340,Human_Splice_Rec_1784358 RMVar_hsa_circ_4506,RMVar_hsa_circ_5195,RMVar_hsa_circ_182331,RMVar_hsa_circ_117464 60235 RMVar_ID_60235 Human_SNP_ID_618765882 m1A Human chr17 + 16440234 16440234 16440234 AATCAGCATCATGTTTGGCAGCTGAGTATTGGAGCCAGGAGCCTGCCATGAGGTAAGCCTTGCTC AATCAGCATCATGTTTGGCAGCTGAGTATTGGGGCCAGGAGCCTGCCATGAGGTAAGCCTTGCTC A G SNHG29 Ensembl:ENSG00000175061 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16440144..16440291 26863196 MeRIP-seq:(Medium) rs1330850133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483855,Human_RBP_ID_899466,Human_RBP_ID_1131912,Human_RBP_ID_1528476,Human_RBP_ID_1849836,Human_RBP_ID_3513488,Human_RBP_ID_4467532,Human_RBP_ID_5088431,Human_RBP_ID_5366398,Human_RBP_ID_5579996,Human_RBP_ID_5649221,Human_RBP_ID_6563382,Human_RBP_ID_8193418,Human_RBP_ID_8813554,Human_RBP_ID_9069424,Human_RBP_ID_12902249,Human_RBP_ID_17258139,Human_RBP_ID_17654102,Human_RBP_ID_17691304,Human_RBP_ID_17885946,Human_RBP_ID_18438432,Human_RBP_ID_18987973,Human_RBP_ID_22498784,Human_RBP_ID_23128907,Human_RBP_ID_23209840,Human_RBP_ID_23712930 Human_Splice_Rec_1783974,Human_Splice_Rec_1783975,Human_Splice_Rec_1783982,Human_Splice_Rec_1783983,Human_Splice_Rec_1783992,Human_Splice_Rec_1783993,Human_Splice_Rec_1784000,Human_Splice_Rec_1784001,Human_Splice_Rec_1784008,Human_Splice_Rec_1784009,Human_Splice_Rec_1784016,Human_Splice_Rec_1784017,Human_Splice_Rec_1784024,Human_Splice_Rec_1784025,Human_Splice_Rec_1784030,Human_Splice_Rec_1784031,Human_Splice_Rec_1784040,Human_Splice_Rec_1784041,Human_Splice_Rec_1784050,Human_Splice_Rec_1784051,Human_Splice_Rec_1784058,Human_Splice_Rec_1784059,Human_Splice_Rec_1784066,Human_Splice_Rec_1784067,Human_Splice_Rec_1784074,Human_Splice_Rec_1784075,Human_Splice_Rec_1784080,Human_Splice_Rec_1784081,Human_Splice_Rec_1784094,Human_Splice_Rec_1784095,Human_Splice_Rec_1784099,Human_Splice_Rec_1784106,Human_Splice_Rec_1784107,Human_Splice_Rec_1784117,Human_Splice_Rec_1784124,Human_Splice_Rec_1784125,Human_Splice_Rec_1784130,Human_Splice_Rec_1784131,Human_Splice_Rec_1784135,Human_Splice_Rec_1784143,Human_Splice_Rec_1784152,Human_Splice_Rec_1784153,Human_Splice_Rec_1784158,Human_Splice_Rec_1784159,Human_Splice_Rec_1784168,Human_Splice_Rec_1784169,Human_Splice_Rec_1784178,Human_Splice_Rec_1784179,Human_Splice_Rec_1784188,Human_Splice_Rec_1784189,Human_Splice_Rec_1784196,Human_Splice_Rec_1784197,Human_Splice_Rec_1784203,Human_Splice_Rec_1784213,Human_Splice_Rec_1784218,Human_Splice_Rec_1784219,Human_Splice_Rec_1784226,Human_Splice_Rec_1784227,Human_Splice_Rec_1784238,Human_Splice_Rec_1784239,Human_Splice_Rec_1784248,Human_Splice_Rec_1784249,Human_Splice_Rec_1784256,Human_Splice_Rec_1784257,Human_Splice_Rec_1784267,Human_Splice_Rec_1784269,Human_Splice_Rec_1784274,Human_Splice_Rec_1784275,Human_Splice_Rec_1784278,Human_Splice_Rec_1784279,Human_Splice_Rec_1784286,Human_Splice_Rec_1784287,Human_Splice_Rec_1784296,Human_Splice_Rec_1784297,Human_Splice_Rec_1784302,Human_Splice_Rec_1784303,Human_Splice_Rec_1784308,Human_Splice_Rec_1784309,Human_Splice_Rec_1784316,Human_Splice_Rec_1784317,Human_Splice_Rec_1784324,Human_Splice_Rec_1784325,Human_Splice_Rec_1784330,Human_Splice_Rec_1784331,Human_Splice_Rec_1784342,Human_Splice_Rec_1784343,Human_Splice_Rec_1784350,Human_Splice_Rec_1784351,Human_Splice_Rec_1784360,Human_Splice_Rec_1784361 Human_miRNA_ID_2084102,Human_miRNA_ID_2418607,Human_miRNA_ID_3154717,Human_miRNA_ID_3174484 RMVar_hsa_circ_4506,RMVar_hsa_circ_43320,RMVar_hsa_circ_182333,RMVar_hsa_circ_78035 60236 RMVar_ID_60236 Human_SNP_ID_618766258 m1A Human chr17 - 16441341 16441338 16441342 TATAACCTGCAAAGAAACTACATTTCAATCTCACTTTCTGCACCAACTGACAGTCAATCACAGGG TATAACCTGCAAAGAAACTACATTTCAATCT____TTCTGCACCAACTGACAGTCAATCACAGGG AAGTG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16441339..16441506 26863196 MeRIP-seq:(Medium) rs771308391 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_18689973 60237 RMVar_ID_60237 Human_SNP_ID_618768872 m1A Human chr17 + 16450799 16450799 16450799 GAGGGGTGGACAGGAGGTGGAGAGGATGACTCAGGGCCAGGCTATTGGAAGGGGCTGAGGGGACA GAGGGGTGGACAGGAGGTGGAGAGGATGACTCGGGGCCAGGCTATTGGAAGGGGCTGAGGGGACA A G SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16450759..16451198 26863196 MeRIP-seq:(Medium) rs1347424237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5581558,Human_RBP_ID_6563596,Human_RBP_ID_12902801,Human_RBP_ID_17189791 60238 RMVar_ID_60238 Human_SNP_ID_618768927 m1A Human chr17 + 16451099 16451099 16451099 TCCAGGCTGGACACATTCATCAGTAAGATTAAACCCCTGGCCAGAGAATGAGCTAAGCAGGAGGG TCCAGGCTGGACACATTCATCAGTAAGATTAAGCCCCTGGCCAGAGAATGAGCTAAGCAGGAGGG A G SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16450746..16451234 26863196 MeRIP-seq:(Medium) rs927256047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12902813,Human_RBP_ID_23308018,Human_RBP_ID_26331349 60239 RMVar_ID_60239 Human_SNP_ID_618770727 m1A Human chr17 + 16456434 16456431 16456435 GGAAGAGGAGGAGGAGGAAGAGGAGCAGAAGAAGGAAGAGGAGGAGGAAGAGGAAGAAGAGGAGA GGAAGAGGAGGAGGAGGAAGAGGAGCAGAA____GAAGAGGAGGAGGAAGAGGAAGAAGAGGAGA AGAAG A SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:16456161..16456633 26863196 MeRIP-seq:(Medium) rs1253028980 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_8254392,Human_RBP_ID_22947377,Human_RBP_ID_24544803 60240 RMVar_ID_60240 Human_SNP_ID_618770731 m1A Human chr17 + 16456438 16456438 16456438 GAGGAGGAGGAGGAAGAGGAGCAGAAGAAGGAAGAGGAGGAGGAAGAGGAAGAAGAGGAGAAGGA GAGGAGGAGGAGGAAGAGGAGCAGAAGAAGGAGGAGGAGGAGGAAGAGGAAGAAGAGGAGAAGGA A G SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16456142..16456647 26863196 MeRIP-seq:(Medium) rs1363874695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254392,Human_RBP_ID_22947377,Human_RBP_ID_24544803 60241 RMVar_ID_60241 Human_SNP_ID_618779505 m1A Human chr17 - 16491948 16491948 16491948 GGCAGACCAAGGGCAGCCTGGCGGAGAGAGCCAGCCCCGGCGCCGCGCCGGGCCCCCGACGCGAA GGCAGACCAAGGGCAGCCTGGCGGAGAGAGCCGGCCCCGGCGCCGCGCCGGGCCCCCGACGCGAA T C LRRC75A Ensembl:ENSG00000181350 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:16491896..16492048 26863196 MeRIP-seq:(Medium) rs1293428642 Functional Loss SNV dbSNP153 33..33 33 - - - 60242 RMVar_ID_60242 Human_SNP_ID_618868599 m1A Human chr17 + 16871060 16871060 16871060 GGCACGTGAAGATGGGGCTCCAGGAAGGGGACATGAACACAGCAGTTCTTGGGGCTTTCTCCTTC GGCACGTGAAGATGGGGCTCCAGGAAGGGGACCTGAACACAGCAGTTCTTGGGGCTTTCTCCTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:16871032..16871166 26863196 MeRIP-seq:(Medium) rs1290563913 Functional Loss SNV dbSNP153 33..33 33 - - - 60243 RMVar_ID_60243 Human_SNP_ID_618913092 m1A Human chr17 - 17042832 17042811 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG_____________________CAGGCCTGGCCG GCGCCGCCGCCGCCGCCGCCGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs980998209 Functional Loss DEL dbSNP153 33..53 33 - - - 60244 RMVar_ID_60244 Human_SNP_ID_618913103 m1A Human chr17 - 17042832 17042814 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG__________________GCGCAGGCCTGGCCG CCGCCGCCGCCGCCGCCGT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs773362138 Functional Loss DEL dbSNP153 33..50 33 - - - 60245 RMVar_ID_60245 Human_SNP_ID_618913106 m1A Human chr17 - 17042832 17042817 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG_______________GCGGCGCAGGCCTGGCCG CCGCCGCCGCCGCCGT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs1346182294 Functional Loss DEL dbSNP153 33..47 33 - - - 60246 RMVar_ID_60246 Human_SNP_ID_618913109 m1A Human chr17 - 17042832 17042820 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG____________GCGGCGGCGCAGGCCTGGCCG CCGCCGCCGCCGT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs749266518 Functional Loss DEL dbSNP153 33..44 33 - - - 60247 RMVar_ID_60247 Human_SNP_ID_618913114 m1A Human chr17 - 17042832 17042823 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG_________GCGGCGGCGGCGCAGGCCTGGCCG CCGCCGCCGT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs1190574837 Functional Loss DEL dbSNP153 33..41 33 - - - 60248 RMVar_ID_60248 Human_SNP_ID_618913117 m1A Human chr17 - 17042832 17042826 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG______GCGGCGGCGGCGGCGCAGGCCTGGCCG CCGCCGT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs774499369 Functional Loss DEL dbSNP153 33..38 33 - - - 60249 RMVar_ID_60249 Human_SNP_ID_618913125 m1A Human chr17 - 17042832 17042831 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCG_CGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs1555556338 Functional Loss DEL dbSNP153 33..33 33 - - - 60250 RMVar_ID_60250 Human_SNP_ID_618913126 m1A Human chr17 - 17042832 17042832 17042832 CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGACGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG CCTTGGCTGCCGACATGGTCGGCGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGCAGGCCTGGCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17042517..17042907 26863196 MeRIP-seq:(Medium) rs779512475 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 60251 RMVar_ID_60251 Human_SNP_ID_618917238 m1A Human chr17 + 17058510 17058510 17058510 GTGGGGAGTGGGGACCCGGGGAGGAGAGCCCCAGGGGCCATGGAGAGTGGGGACCCAGGGAGGAG GTGGGGAGTGGGGACCCGGGGAGGAGAGCCCCGGGGGCCATGGAGAGTGGGGACCCAGGGAGGAG A G MPRIP Ensembl:ENSG00000133030 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17058480..17058551 26863196 MeRIP-seq:(Medium) rs1204278543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26782038 RMVar_hsa_circ_182341,RMVar_hsa_circ_127450 60252 RMVar_ID_60252 Human_SNP_ID_618917241 m1A Human chr17 + 17058521 17058521 17058521 GGACCCGGGGAGGAGAGCCCCAGGGGCCATGGAGAGTGGGGACCCAGGGAGGAGAGCTCCAGGGA GGACCCGGGGAGGAGAGCCCCAGGGGCCATGGGGAGTGGGGACCCAGGGAGGAGAGCTCCAGGGA A G MPRIP Ensembl:ENSG00000133030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17058292..17058658 26863196 MeRIP-seq:(Medium) rs1230587958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26782038 RMVar_hsa_circ_182341,RMVar_hsa_circ_127450 60253 RMVar_ID_60253 Human_SNP_ID_618922931 m1A Human chr17 - 17081478 17081476 17081479 TCCCTTCTGCTGAGTAATCCCTAAAGGTCACTACATTGCTAATCTCCCTCCGAGGAACACCCCTT TCCCTTCTGCTGAGTAATCCCTAAAGGTCAC___ATTGCTAATCTCCCTCCGAGGAACACCCCTT TGTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17081463..17081556 26863196 MeRIP-seq:(Medium) rs552049638 Functional Loss DEL dbSNP153 32..34 33 - - - 60254 RMVar_ID_60254 Human_SNP_ID_618935685 m1A Human chr17 - 17131703 17131703 17131703 TGAGGGGATGCCATCTGGCAAACCCACTGCCTACCTGTGGTGTGGGGGGCTCCACTTTCCGTTTC TGAGGGGATGCCATCTGGCAAACCCACTGCCTGCCTGTGGTGTGGGGGGCTCCACTTTCCGTTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17131680..17131758 26863196 MeRIP-seq:(Medium) rs1260742962 Functional Loss SNV dbSNP153 33..33 33 - - - 60255 RMVar_ID_60255 Human_SNP_ID_618936778 m1A Human chr17 + 17136099 17136099 17136099 CTCACTGTTTTGGGGCAGTATCTGAAGATTCCAGGCCCCTGACATTGTGTAGCTGGCCCGGGTGC CTCACTGTTTTGGGGCAGTATCTGAAGATTCCGGGCCCCTGACATTGTGTAGCTGGCCCGGGTGC A G MPRIP Ensembl:ENSG00000133030 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:17136098..17136325 26863196 MeRIP-seq:(Medium) rs939199582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76119,RMVar_hsa_circ_102997,RMVar_hsa_circ_118635,RMVar_hsa_circ_127754,RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_108633,RMVar_hsa_circ_103498,RMVar_hsa_circ_92104,RMVar_hsa_circ_99928,RMVar_hsa_circ_101023,RMVar_hsa_circ_99099,RMVar_hsa_circ_85121,RMVar_hsa_circ_86770,RMVar_hsa_circ_16167,RMVar_hsa_circ_182346,RMVar_hsa_circ_182350,RMVar_hsa_circ_182354,RMVar_hsa_circ_182356,RMVar_hsa_circ_182355,RMVar_hsa_circ_182352,RMVar_hsa_circ_182353,RMVar_hsa_circ_182351,RMVar_hsa_circ_182348,RMVar_hsa_circ_182349,RMVar_hsa_circ_182347,RMVar_hsa_circ_118056,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_182360,RMVar_hsa_circ_81406,RMVar_hsa_circ_82985,RMVar_hsa_circ_182361,RMVar_hsa_circ_100905,RMVar_hsa_circ_182359,RMVar_hsa_circ_182365,RMVar_hsa_circ_370825,RMVar_hsa_circ_182366 60256 RMVar_ID_60256 Human_SNP_ID_618936852 m1A Human chr17 + 17136258 17136258 17136258 GGCCTGCCAAGGTGGCTGTTACCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCATCCCCAGT GGCCTGCCAAGGTGGCTGTTACCAGCAGCAGCGGCAGCAGCAGCAGCAGCAGCAGCATCCCCAGT A G MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17136226..17136325 26863196 MeRIP-seq:(Medium) rs1256264516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143755,Human_RBP_ID_18987979,Human_RBP_ID_26955358 Human_Splice_Rec_1784992,Human_Splice_Rec_1785046,Human_Splice_Rec_1785090,Human_Splice_Rec_1785128,Human_Splice_Rec_1785132 RMVar_hsa_circ_76119,RMVar_hsa_circ_102997,RMVar_hsa_circ_118635,RMVar_hsa_circ_127754,RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_108633,RMVar_hsa_circ_103498,RMVar_hsa_circ_92104,RMVar_hsa_circ_99928,RMVar_hsa_circ_101023,RMVar_hsa_circ_99099,RMVar_hsa_circ_85121,RMVar_hsa_circ_86770,RMVar_hsa_circ_16167,RMVar_hsa_circ_182346,RMVar_hsa_circ_182350,RMVar_hsa_circ_182354,RMVar_hsa_circ_182356,RMVar_hsa_circ_182355,RMVar_hsa_circ_182352,RMVar_hsa_circ_182353,RMVar_hsa_circ_182351,RMVar_hsa_circ_182348,RMVar_hsa_circ_182349,RMVar_hsa_circ_182347,RMVar_hsa_circ_118056,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_182360,RMVar_hsa_circ_81406,RMVar_hsa_circ_82985,RMVar_hsa_circ_182361,RMVar_hsa_circ_100905,RMVar_hsa_circ_182359,RMVar_hsa_circ_182365,RMVar_hsa_circ_370825,RMVar_hsa_circ_103287,RMVar_hsa_circ_182366,RMVar_hsa_circ_182367 60257 RMVar_ID_60257 Human_SNP_ID_618938473 m1A Human chr17 - 17142303 17142303 17142303 CTCTCCTGAGCCACAGACATGATCAAAAGGCAACCACCACCACGGAAGGCAGCCTCCATTCTCAT CTCTCCTGAGCCACAGACATGATCAAAAGGCACCCACCACCACGGAAGGCAGCCTCCATTCTCAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:17142298..17142432;chr17:17142301..17142419 26863196 MeRIP-seq:(Medium) rs1362425394 Functional Loss SNV dbSNP153 33..33 33 - - - 60258 RMVar_ID_60258 Human_SNP_ID_618941719 m1A Human chr17 + 17154393 17154393 17154393 GGATCCAGACCATCATGAAGCACGTGCACCCGACCACTGCCCCGGATGTGACCAGGTAGGATGGT GGATCCAGACCATCATGAAGCACGTGCACCCGTCCACTGCCCCGGATGTGACCAGGTAGGATGGT A T MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17154344..17154467 26863196 MeRIP-seq:(Medium) rs777305702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236232,Human_RBP_ID_5525376,Human_RBP_ID_6564270,Human_RBP_ID_8824457,Human_RBP_ID_9288797,Human_RBP_ID_19081633 Human_Splice_Rec_1785006,Human_Splice_Rec_1785007,Human_Splice_Rec_1785060,Human_Splice_Rec_1785061,Human_Splice_Rec_1785104,Human_Splice_Rec_1785105,Human_Splice_Rec_1785144,Human_Splice_Rec_1785145,Human_Splice_Rec_1785174,Human_Splice_Rec_1785175,Human_Splice_Rec_1785177 Human_miRNA_ID_2458093,Human_miRNA_ID_2463017,Human_miRNA_ID_2635657,Human_miRNA_ID_2638344 RMVar_hsa_circ_127754,RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_101023,RMVar_hsa_circ_99099,RMVar_hsa_circ_85121,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182350,RMVar_hsa_circ_182351,RMVar_hsa_circ_182348,RMVar_hsa_circ_182349,RMVar_hsa_circ_182347,RMVar_hsa_circ_118056,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_182360,RMVar_hsa_circ_81406,RMVar_hsa_circ_182361,RMVar_hsa_circ_5740,RMVar_hsa_circ_3515,RMVar_hsa_circ_92989,RMVar_hsa_circ_119486,RMVar_hsa_circ_55208,RMVar_hsa_circ_182368,RMVar_hsa_circ_182369,RMVar_hsa_circ_333553,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_9571,RMVar_hsa_circ_182372,RMVar_hsa_circ_303896,RMVar_hsa_circ_275561,RMVar_hsa_circ_182373 60259 RMVar_ID_60259 Human_SNP_ID_618942913 m1A Human chr17 - 17158742 17158742 17158742 GCCTGGCCCGTCTGTGGCGTCGAGCATCCCGAAGCGCTTGCGGCGCTCCTCCCGCCTCCGTGCAC GCCTGGCCCGTCTGTGGCGTCGAGCATCCCGACGCGCTTGCGGCGCTCCTCCCGCCTCCGTGCAC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:17158476..17158900 26863196 MeRIP-seq:(Medium) rs1457908349 Functional Loss SNV dbSNP153 33..33 33 - - - 60260 RMVar_ID_60260 Human_SNP_ID_618942969 m1A Human chr17 + 17158847 17158847 17158847 CAGGGCTGCCTATGAGCGACCTCAAAACGCATAACGTCCACGTGGAGATTGAGCAGCGGTGGCAT CAGGGCTGCCTATGAGCGACCTCAAAACGCATGACGTCCACGTGGAGATTGAGCAGCGGTGGCAT A G MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:17158501..17158900 26863196 MeRIP-seq:(Medium) rs775123897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48137,Human_RBP_ID_1849985,Human_RBP_ID_8445374,Human_RBP_ID_8813618,Human_RBP_ID_9289860,Human_RBP_ID_9377649,Human_RBP_ID_18987985,Human_RBP_ID_27813501 RMVar_hsa_circ_127754,RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_101023,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182350,RMVar_hsa_circ_182348,RMVar_hsa_circ_182349,RMVar_hsa_circ_182347,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_81406,RMVar_hsa_circ_182361,RMVar_hsa_circ_5740,RMVar_hsa_circ_3515,RMVar_hsa_circ_119486,RMVar_hsa_circ_55208,RMVar_hsa_circ_182369,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854 60261 RMVar_ID_60261 Human_SNP_ID_618945444 m1A Human chr17 - 17167199 17167199 17167199 CTGCTCTGAGCAGGAGGGCTCCCGGGTTTGCCAGGACTCCTTGCAGAGCTGGAGCTCCTTCTCAT CTGCTCTGAGCAGGAGGGCTCCCGGGTTTGCCGGGACTCCTTGCAGAGCTGGAGCTCCTTCTCAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17167192..17167492 32194978 MeRIP-seq:(Medium) rs1463077851 Functional Loss SNV dbSNP153 33..33 33 - - - 60262 RMVar_ID_60262 Human_SNP_ID_618945498 m1A Human chr17 + 17167346 17167346 17167346 TTGTTGAAAGGGAGAATGCAGAGCTCAAGGCCAAGGCCGCCCAGCTAGACCATCAGCAGCAGTGT TTGTTGAAAGGGAGAATGCAGAGCTCAAGGCCGAGGCCGCCCAGCTAGACCATCAGCAGCAGTGT A G MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17167345..17167577 26863196 MeRIP-seq:(Medium) rs1261064732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48166,Human_RBP_ID_22715696 RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182348,RMVar_hsa_circ_182347,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_55208,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374 60263 RMVar_ID_60263 Human_SNP_ID_618945514 m1A Human chr17 + 17167394 17167394 17167394 ACCATCAGCAGCAGTGTCTGGAGGATGCAGAGAGCAAGCACAGCATGAGCATGTTCACCCTGCGG ACCATCAGCAGCAGTGTCTGGAGGATGCAGAGGGCAAGCACAGCATGAGCATGTTCACCCTGCGG A G MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17167385..17167611 26863196 MeRIP-seq:(Medium) rs1464819583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48166 RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182348,RMVar_hsa_circ_182347,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_55208,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374 60264 RMVar_ID_60264 Human_SNP_ID_618945515 m1A Human chr17 + 17167394 17167394 17167394 ACCATCAGCAGCAGTGTCTGGAGGATGCAGAGAGCAAGCACAGCATGAGCATGTTCACCCTGCGG ACCATCAGCAGCAGTGTCTGGAGGATGCAGAGTGCAAGCACAGCATGAGCATGTTCACCCTGCGG A T MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17167385..17167611 26863196 MeRIP-seq:(Medium) rs1464819583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48166 RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182348,RMVar_hsa_circ_182347,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_55208,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374 60265 RMVar_ID_60265 Human_SNP_ID_618945551 m1A Human chr17 + 17167484 17167484 17167485 GTGTGGTGGAGCAGCTGACCAGGACCGAGAGCACACTGCAGGCTGAGCGCAGCCGGGTCCTGAGC GTGTGGTGGAGCAGCTGACCAGGACCGAGAGCGGACTGCAGGCTGAGCGCAGCCGGGTCCTGAGC AC GG MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17167475..17167549 26863196 MeRIP-seq:(Medium) rs868767144 Functional Loss MNV dbSNP153 33..34 33 - - - Human_RBP_ID_896227,Human_RBP_ID_22209658 RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182348,RMVar_hsa_circ_182347,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_55208,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374 60266 RMVar_ID_60266 Human_SNP_ID_618948103 m1A Human chr17 + 17176501 17176501 17176501 AGGAGATTAGCTCCCTCAAGGATGAGCTGCAGACGGCACTGCGGGTAAGGCCACCGCACCACAGG AGGAGATTAGCTCCCTCAAGGATGAGCTGCAGTCGGCACTGCGGGTAAGGCCACCGCACCACAGG A T MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17176476..17176500 26863196 MeRIP-seq:(Medium) rs767497368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821955,Human_RBP_ID_18987987,Human_RBP_ID_26331359 Human_Splice_Rec_1785022,Human_Splice_Rec_1785023,Human_Splice_Rec_1785074,Human_Splice_Rec_1785075,Human_Splice_Rec_1785118,Human_Splice_Rec_1785119,Human_Splice_Rec_1785158,Human_Splice_Rec_1785159,Human_Splice_Rec_1785192,Human_Splice_Rec_1785193,Human_Splice_Rec_1785208,Human_Splice_Rec_1785209,Human_Splice_Rec_1785224,Human_Splice_Rec_1785225,Human_Splice_Rec_1785232,Human_Splice_Rec_1785233,Human_Splice_Rec_1785236,Human_Splice_Rec_1785237 RMVar_hsa_circ_103498,RMVar_hsa_circ_99928,RMVar_hsa_circ_99099,RMVar_hsa_circ_86770,RMVar_hsa_circ_182346,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_73560,RMVar_hsa_circ_6854,RMVar_hsa_circ_64299,RMVar_hsa_circ_182377,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374,RMVar_hsa_circ_376011,RMVar_hsa_circ_280167,RMVar_hsa_circ_182376,RMVar_hsa_circ_282845,RMVar_hsa_circ_283197,RMVar_hsa_circ_122407,RMVar_hsa_circ_368378,RMVar_hsa_circ_10588,RMVar_hsa_circ_45194,RMVar_hsa_circ_182378 60267 RMVar_ID_60267 Human_SNP_ID_618950328 m1A Human chr17 - 17184925 17184925 17184925 CAGCGCTTGGGGTGTGCTGCTGCAAGCTGGGGAAGGCGCGTGCTCAACTTGGATGGGACACACCT CAGCGCTTGGGGTGTGCTGCTGCAAGCTGGGGGAGGCGCGTGCTCAACTTGGATGGGACACACCT T C AC055811.1 Ensembl:ENSG00000263624 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17184876..17184950 26863196 MeRIP-seq:(Medium) rs909936135 Functional Loss SNV dbSNP153 33..33 33 - - - 60268 RMVar_ID_60268 Human_SNP_ID_618956574 m1A Human chr17 + 17206271 17206271 17206271 CAGGCCCACAGCCGCCGCGGCCGCCACCTGCCAACTCAACCGTCCCATGCCGCCGCTAATCCGGG CAGGCCCACAGCCGCCGCGGCCGCCACCTGCCTACTCAACCGTCCCATGCCGCCGCTAATCCGGG A T MPRIP Ensembl:ENSG00000133030 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:17206170..17206338;chr17:17206039..17206400 26863196 MeRIP-seq:(Medium) rs1411606207 Functional Loss SNV dbSNP153 33..33 33 - - - 60269 RMVar_ID_60269 Human_SNP_ID_618956575 m1A Human chr17 - 17206274 17206274 17206274 GGTCCCGGATTAGCGGCGGCATGGGACGGTTGAGTTGGCAGGTGGCGGCCGCGGCGGCTGTGGGC GGTCCCGGATTAGCGGCGGCATGGGACGGTTGGGTTGGCAGGTGGCGGCCGCGGCGGCTGTGGGC T C PLD6,AC055811.2 Ensembl:ENSG00000179598,Ensembl:ENSG00000264187 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17206019..17206337 26863196 MeRIP-seq:(Medium) rs1163030994 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_767486,Human_RBP_ID_18419546 60270 RMVar_ID_60270 Human_SNP_ID_618961325 m1A Human chr17 - 17221440 17221437 17221441 GCTCTCCTGGCAGGAATCGCTGAGGGAGGGAAACGCGGCTCTGAATCAGCCCAGAACGAGCCTTC GCTCTCCTGGCAGGAATCGCTGAGGGAGGGA____CGGCTCTGAATCAGCCCAGAACGAGCCTTC GCGTT G FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr17:17221400..17221485;chr17:17221436..17221508 26863410,26863196 MeRIP-seq:(Medium) rs780928989 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_897383,Human_RBP_ID_9346165,Human_RBP_ID_12906559,Human_RBP_ID_17128096,Human_RBP_ID_19085891,Human_RBP_ID_22658436,Human_RBP_ID_23713356,Human_RBP_ID_26331360,Human_RBP_ID_26781125 RMVar_hsa_circ_2718,RMVar_hsa_circ_341830,RMVar_hsa_circ_10993,RMVar_hsa_circ_28716,RMVar_hsa_circ_265639 60271 RMVar_ID_60271 Human_SNP_ID_618971536 m1A Human chr17 - 17258945 17258945 17258945 GAGGAAGGAAGGTGAGGAGAGGGTCAATGGGCAAGAAAAAGAATCCTTCCAAATACTCTAGAAAG GAGGAAGGAAGGTGAGGAGAGGGTCAATGGGCCAGAAAAAGAATCCTTCCAAATACTCTAGAAAG T G COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17258943..17259029 26863196 MeRIP-seq:(Medium) rs1418658182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9847118,Human_RBP_ID_12907245 RMVar_hsa_circ_280000,RMVar_hsa_circ_182391,RMVar_hsa_circ_75079,RMVar_hsa_circ_330730,RMVar_hsa_circ_310596,RMVar_hsa_circ_343779,RMVar_hsa_circ_355939,RMVar_hsa_circ_285471,RMVar_hsa_circ_182393,RMVar_hsa_circ_182394,RMVar_hsa_circ_182392 60272 RMVar_ID_60272 Human_SNP_ID_618972289 m1A Human chr17 - 17262000 17262000 17262000 GATATTACTTGGCAAAGTACAACAGCTACCAAAATATACATCTCAAATTGTGGGTAGATTCATTA GATATTACTTGGCAAAGTACAACAGCTACCAACATATACATCTCAAATTGTGGGTAGATTCATTA T G COPS3 Ensembl:ENSG00000141030 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:17261976..17262050 32194978 MeRIP-seq:(Medium) rs760861624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1006476,Human_RBP_ID_1367239,Human_RBP_ID_1850145,Human_RBP_ID_8088965,Human_RBP_ID_9078467,Human_RBP_ID_9257289,Human_RBP_ID_17258193,Human_RBP_ID_17374169,Human_RBP_ID_17489304,Human_RBP_ID_17691330,Human_RBP_ID_17886202,Human_RBP_ID_22498813,Human_RBP_ID_22947463,Human_RBP_ID_27662134 Human_Splice_Rec_1785351,Human_Splice_Rec_1785373,Human_Splice_Rec_1785399,Human_Splice_Rec_1785421,Human_Splice_Rec_1785441,Human_Splice_Rec_1785451,Human_Splice_Rec_1785465,Human_Splice_Rec_1785479 Human_miRNA_ID_1381800,Human_miRNA_ID_2379619 RMVar_hsa_circ_4231,RMVar_hsa_circ_75079,RMVar_hsa_circ_310596,RMVar_hsa_circ_343779,RMVar_hsa_circ_355939,RMVar_hsa_circ_285471,RMVar_hsa_circ_182393,RMVar_hsa_circ_182394,RMVar_hsa_circ_352019,RMVar_hsa_circ_269985,RMVar_hsa_circ_25078,RMVar_hsa_circ_25363,RMVar_hsa_circ_182396,RMVar_hsa_circ_17684,RMVar_hsa_circ_182397,RMVar_hsa_circ_182399,RMVar_hsa_circ_276589,RMVar_hsa_circ_182398,RMVar_hsa_circ_292497,RMVar_hsa_circ_182400 60273 RMVar_ID_60273 Human_SNP_ID_618976230 m1A Human chr17 + 17277002 17277002 17277002 GAACTAAGGCCCTTCAATAACTGGTCCCTGCTACCTTTCCAGCCTTATCTCCTGCTACTTCCCCT GAACTAAGGCCCTTCAATAACTGGTCCCTGCTGCCTTTCCAGCCTTATCTCCTGCTACTTCCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17276997..17277067 26863196 MeRIP-seq:(Medium) rs78954673 Functional Loss SNV dbSNP153 33..33 33 - - - 60274 RMVar_ID_60274 Human_SNP_ID_618977460 m1A Human chr17 - 17281191 17281191 17281191 GTGCTGCCTTCGCCGCTCGGGCCGCCCGGGGGAAAACATGGCGTCTGCCCTGGAGCAGTTCGTGA GTGCTGCCTTCGCCGCTCGGGCCGCCCGGGGGCAAACATGGCGTCTGCCCTGGAGCAGTTCGTGA T G COPS3 Ensembl:ENSG00000141030 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17281098..17281251 26863196 MeRIP-seq:(Medium) rs1338592334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6229,Human_RBP_ID_237865,Human_RBP_ID_4464356,Human_RBP_ID_9327200 Human_Splice_Rec_1785339,Human_Splice_Rec_1785387,Human_Splice_Rec_1785443,Human_Splice_Rec_1785453,Human_Splice_Rec_1785469,Human_Splice_Rec_1785487,Human_Splice_Rec_1785499,Human_Splice_Rec_1785509,Human_Splice_Rec_1785523 60275 RMVar_ID_60275 Human_SNP_ID_618983144 m1A Human chr17 - 17303465 17303463 17303466 CCGGAGCCGGCCAGACATTCCCGCCGCGGAGGAGAAGCCCCCAACGCTGGGGCGCGCGTGGAGCG CCGGAGCCGGCCAGACATTCCCGCCGCGGAG___AAGCCCCCAACGCTGGGGCGCGCGTGGAGCG TCTC T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:17303368..17303629 26863410 MeRIP-seq:(Medium) rs1394372485 Functional Loss DEL dbSNP153 32..34 33 - - - 60276 RMVar_ID_60276 Human_SNP_ID_618983206 m1A Human chr17 + 17303646 17303628 17303646 CGCGGGGCGGCGGGCGGGCTGGGCCTGGCGGGAGGCCGCGCCCTACGGGTGCTGGTGGACATGGA CGCGGGGCGGCGGGC__________________GGCCGCGCCCTACGGGTGCTGGTGGACATGGA CGGGCTGGGCCTGGCGGGA C NT5M Ensembl:ENSG00000205309 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17303415..17303674 26863196 MeRIP-seq:(Medium) rs756600274 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_5237589,Human_RBP_ID_9327202,Human_RBP_ID_26781127 RMVar_hsa_circ_118122,RMVar_hsa_circ_182405 60277 RMVar_ID_60277 Human_SNP_ID_619003937 m1A Human chr17 - 17383352 17383352 17383352 AAAAATAAAGCCCTCCTGGGGACTTGGAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAGGAGGTT AAAAATAAAGCCCTCCTGGGGACTTGGAATAACAAAAAAAAAAAAAAAAAAAAAAAAAGGAGGTT T G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1387363557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238466,Human_RBP_ID_9069528,Human_RBP_ID_22947469,Human_RBP_ID_26447595,Human_RBP_ID_26955641 60278 RMVar_ID_60278 Human_SNP_ID_619027430 m1A Human chr17 + 17477103 17477103 17477103 ACAGGCGGAGGATGTATTGCCGCCAACGTCCGACCAGCCGCTGCCTGACACCAAGCCGCTGCCGC ACAGGCGGAGGATGTATTGCCGCCAACGTCCGCCCAGCCGCTGCCTGACACCAAGCCGCTGCCGC A C MED9 Ensembl:ENSG00000141026 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17477052..17477141 26863196 MeRIP-seq:(Medium) rs917990887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1528824,Human_RBP_ID_12907928 60279 RMVar_ID_60279 Human_SNP_ID_619027444 m1A Human chr17 - 17477140 17477140 17477140 TGCGGTTGAGGCGCAGGGACCGGCGGCGGCTGAGGAGGCGGCAGCGGCTTGGTGTCAGGCAGCGG TGCGGTTGAGGCGCAGGGACCGGCGGCGGCTGGGGAGGCGGCAGCGGCTTGGTGTCAGGCAGCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:17477051..17477225 26863410 MeRIP-seq:(Medium) rs570173732 Functional Loss SNV dbSNP153 33..33 33 - - - 60280 RMVar_ID_60280 Human_SNP_ID_619036446 m1A Human chr17 - 17509525 17509525 17509525 CCTCATCCACAGGTGATTACTTCGGGATCCTCAAGGAGGCGAGAGTGACCGTGTTCCCCTTCAAC CCTCATCCACAGGTGATTACTTCGGGATCCTCGAGGAGGCGAGAGTGACCGTGTTCCCCTTCAAC T C PEMT Ensembl:ENSG00000133027 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17509451..17509525 32194978 MeRIP-seq:(Medium) rs761000841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484247,Human_RBP_ID_1006499,Human_RBP_ID_17886249,Human_RBP_ID_26813219 Human_Splice_Rec_1785598,Human_Splice_Rec_1785599,Human_Splice_Rec_1785606,Human_Splice_Rec_1785607,Human_Splice_Rec_1785618,Human_Splice_Rec_1785619,Human_Splice_Rec_1785630,Human_Splice_Rec_1785631,Human_Splice_Rec_1785642,Human_Splice_Rec_1785643,Human_Splice_Rec_1785656,Human_Splice_Rec_1785657,Human_Splice_Rec_1785668,Human_Splice_Rec_1785669,Human_Splice_Rec_1785682,Human_Splice_Rec_1785683,Human_Splice_Rec_1785694,Human_Splice_Rec_1785695,Human_Splice_Rec_1785702 RMVar_hsa_circ_19370 60281 RMVar_ID_60281 Human_SNP_ID_619036811 m1A Human chr17 + 17510859 17510859 17510859 CTGCAGCCCTCCCTGTCCAGATCCACCCGAGCACTGGCCACTGGAGGGCCCCCGCCGCTGGTCTC CTGCAGCCCTCCCTGTCCAGATCCACCCGAGCCCTGGCCACTGGAGGGCCCCCGCCGCTGGTCTC A C AC020558.6 Ensembl:ENSG00000286430 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17510659..17511355 26863196 MeRIP-seq:(Medium) rs1286773628 Functional Loss SNV dbSNP153 33..33 33 - - - 60282 RMVar_ID_60282 Human_SNP_ID_619037010 m1A Human chr17 - 17511575 17511575 17511575 GGCTTCAGTGGCCTCAGTAGCCTCCTGGGACCAACGGTGTCCTGAGGAGCTCCCGGGCCTGCCTG GGCTTCAGTGGCCTCAGTAGCCTCCTGGGACCGACGGTGTCCTGAGGAGCTCCCGGGCCTGCCTG T C PEMT Ensembl:ENSG00000133027 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17511570..17511676 32194978 MeRIP-seq:(Medium) rs1007868042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19370 60283 RMVar_ID_60283 Human_SNP_ID_619039681 m1A Human chr17 - 17522283 17522283 17522283 CACCATCCTGCTCCTGAACTTCCTGCGCTCGCACTGGTAAGCACAGCTCTCTCACTGGGGAGCCA CACCATCCTGCTCCTGAACTTCCTGCGCTCGCTCTGGTAAGCACAGCTCTCTCACTGGGGAGCCA T A PEMT Ensembl:ENSG00000133027 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17522276..17522400 26863196 MeRIP-seq:(Medium) rs771507562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081653 Human_Splice_Rec_1785615,Human_Splice_Rec_1785627,Human_Splice_Rec_1785639,Human_Splice_Rec_1785653,Human_Splice_Rec_1785665,Human_Splice_Rec_1785691,Human_Splice_Rec_1785709 RMVar_hsa_circ_19370,RMVar_hsa_circ_60179 60284 RMVar_ID_60284 Human_SNP_ID_619041161 m1A Human chr17 - 17528201 17528201 17528201 GAGATGGGGGCGGTTCGGGAGGCAAAAGCAGGAAGGCAGAAGGAAGCTTGGAGCTCATGAGCCCC GAGATGGGGGCGGTTCGGGAGGCAAAAGCAGGGAGGCAGAAGGAAGCTTGGAGCTCATGAGCCCC T C PEMT Ensembl:ENSG00000133027 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17528195..17528304 26863196 MeRIP-seq:(Medium) rs1373292172 Functional Loss SNV dbSNP153 33..33 33 - - - 60285 RMVar_ID_60285 Human_SNP_ID_619041162 m1A Human chr17 - 17528201 17528201 17528201 GAGATGGGGGCGGTTCGGGAGGCAAAAGCAGGAAGGCAGAAGGAAGCTTGGAGCTCATGAGCCCC GAGATGGGGGCGGTTCGGGAGGCAAAAGCAGGCAGGCAGAAGGAAGCTTGGAGCTCATGAGCCCC T G PEMT Ensembl:ENSG00000133027 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17528195..17528304 26863196 MeRIP-seq:(Medium) rs1373292172 Functional Loss SNV dbSNP153 33..33 33 - - - 60286 RMVar_ID_60286 Human_SNP_ID_619053104 m1A Human chr17 - 17576939 17576939 17576939 CTTTGTGGCTGCCGTCATCACCATCACCTTCAATCCGCTCTACTGGAATGTGGTAAGTGATGTGC CTTTGTGGCTGCCGTCATCACCATCACCTTCAGTCCGCTCTACTGGAATGTGGTAAGTGATGTGC T C PEMT Ensembl:ENSG00000133027 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:17522364..17577415 32194978 MeRIP-seq:(Medium) rs567348854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1850203,Human_RBP_ID_5419848,Human_RBP_ID_17258215,Human_RBP_ID_17374178,Human_RBP_ID_22209841,Human_RBP_ID_22421816,Human_RBP_ID_23275206,Human_RBP_ID_27250321,Human_RBP_ID_27449033 Human_Splice_Rec_1785612,Human_Splice_Rec_1785613,Human_Splice_Rec_1785624,Human_Splice_Rec_1785625,Human_Splice_Rec_1785636,Human_Splice_Rec_1785637,Human_Splice_Rec_1785650,Human_Splice_Rec_1785651,Human_Splice_Rec_1785662,Human_Splice_Rec_1785663,Human_Splice_Rec_1785680,Human_Splice_Rec_1785681,Human_Splice_Rec_1785688,Human_Splice_Rec_1785689,Human_Splice_Rec_1785698,Human_Splice_Rec_1785699,Human_Splice_Rec_1785704,Human_Splice_Rec_1785705 Human_miRNA_ID_830874,Human_miRNA_ID_1351239 60287 RMVar_ID_60287 Human_SNP_ID_619053108 m1A Human chr17 - 17576949 17576949 17576949 TGGATCCCAGCTTTGTGGCTGCCGTCATCACCATCACCTTCAATCCGCTCTACTGGAATGTGGTA TGGATCCCAGCTTTGTGGCTGCCGTCATCACCGTCACCTTCAATCCGCTCTACTGGAATGTGGTA T C PEMT Ensembl:ENSG00000133027 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17576926..17576950 26863196 MeRIP-seq:(Medium) rs781325863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1850203,Human_RBP_ID_4408627,Human_RBP_ID_5419848,Human_RBP_ID_17258215,Human_RBP_ID_17374179,Human_RBP_ID_23275206,Human_RBP_ID_27449033 Human_Splice_Rec_1785612,Human_Splice_Rec_1785613,Human_Splice_Rec_1785624,Human_Splice_Rec_1785625,Human_Splice_Rec_1785636,Human_Splice_Rec_1785637,Human_Splice_Rec_1785650,Human_Splice_Rec_1785651,Human_Splice_Rec_1785662,Human_Splice_Rec_1785663,Human_Splice_Rec_1785680,Human_Splice_Rec_1785681,Human_Splice_Rec_1785688,Human_Splice_Rec_1785689,Human_Splice_Rec_1785698,Human_Splice_Rec_1785699,Human_Splice_Rec_1785704,Human_Splice_Rec_1785705 Human_miRNA_ID_1351239 60288 RMVar_ID_60288 Human_SNP_ID_619057014 m1A Human chr17 - 17591524 17591524 17591524 GCCTCGGCAATATTGATTTTAGACAGGTACTGACCGCACCGGACCGCCGCGGAAACTGGGAGAGG GCCTCGGCAATATTGATTTTAGACAGGTACTGGCCGCACCGGACCGCCGCGGAAACTGGGAGAGG T C PEMT Ensembl:ENSG00000133027 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17591521..17591616 32194978 MeRIP-seq:(Medium) rs1208674222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23713560 60289 RMVar_ID_60289 Human_SNP_ID_619082051 m1A Human chr17 - 17683324 17683322 17683325 GGAGAATGGAGGGGGGCAGGGGCAGGAAGAGAAGCAGAGCCCCCAGCTCGGGGCTCCCATCACGC GGAGAATGGAGGGGGGCAGGGGCAGGAAGAG___CAGAGCCCCCAGCTCGGGGCTCCCATCACGC GCTT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17683317..17683499 32194978 MeRIP-seq:(Medium) rs1220344338 Functional Loss DEL dbSNP153 32..34 33 - - - 60290 RMVar_ID_60290 Human_SNP_ID_619083022 m1A Human chr17 - 17686530 17686530 17686530 AAGAACCAGTGGAGCGAAATCTGTCCTTTGCCAGCCAAGCCCCAGCCTGTACCTCCAAGCCCTGC AAGAACCAGTGGAGCGAAATCTGTCCTTTGCCCGCCAAGCCCCAGCCTGTACCTCCAAGCCCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17686526..17686821 26863196 MeRIP-seq:(Medium) rs1486885236 Functional Loss SNV dbSNP153 33..33 33 - - - 60291 RMVar_ID_60291 Human_SNP_ID_619083281 m1A Human chr17 + 17687138 17687138 17687138 CCAAGTAGCTGGGATTACAGGCGCCCACCACCACGCCCGGCTAGTTGAGCAACCTCTTTCTGCAC CCAAGTAGCTGGGATTACAGGCGCCCACCACCGCGCCCGGCTAGTTGAGCAACCTCTTTCTGCAC A G RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17687134..17687454 26863196 MeRIP-seq:(Medium) rs1185090035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12909199 RMVar_hsa_circ_57371 60292 RMVar_ID_60292 Human_SNP_ID_619088302 m1A Human chr17 + 17706165 17706165 17706165 TGCAGAGCCACGGTGCTTGCCCAGAGGTCAGCAGCCCTATGGGATGCTTGGGGTGGGGCGTCAGA TGCAGAGCCACGGTGCTTGCCCAGAGGTCAGCCGCCCTATGGGATGCTTGGGGTGGGGCGTCAGA A C RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17706161..17706643 26863196 MeRIP-seq:(Medium) rs377715892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57371 60293 RMVar_ID_60293 Human_SNP_ID_619088303 m1A Human chr17 + 17706165 17706165 17706165 TGCAGAGCCACGGTGCTTGCCCAGAGGTCAGCAGCCCTATGGGATGCTTGGGGTGGGGCGTCAGA TGCAGAGCCACGGTGCTTGCCCAGAGGTCAGCGGCCCTATGGGATGCTTGGGGTGGGGCGTCAGA A G RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17706161..17706643 26863196 MeRIP-seq:(Medium) rs377715892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57371 60294 RMVar_ID_60294 Human_SNP_ID_619091999 m1A Human chr17 - 17722012 17722012 17722012 CACACTTGGGTTTTGCTGCTCAATGATGTCCCAATCTCCCTTCTCCACCTACTAACCCCCAACCC CACACTTGGGTTTTGCTGCTCAATGATGTCCCCATCTCCCTTCTCCACCTACTAACCCCCAACCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17722005..17722130 26863196 MeRIP-seq:(Medium) rs1156520042 Functional Loss SNV dbSNP153 33..33 33 - - - 60295 RMVar_ID_60295 Human_SNP_ID_619092354 m1A Human chr17 + 17723119 17723119 17723119 CACGGCCCCACACACCCACCAGCCCACTCGCAAACAGGCCCACATGGCCACACAACTGCCCTCTG CACGGCCCCACACACCCACCAGCCCACTCGCAGACAGGCCCACATGGCCACACAACTGCCCTCTG A G RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17723114..17723279 26863196 MeRIP-seq:(Medium) rs1430292004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57371 60296 RMVar_ID_60296 Human_SNP_ID_619102003 m1A Human chr17 - 17761728 17761728 17761728 CAGGGGATTCCCACCCACCTCCCCAGCTCCCAAATTTCATGCCCAGCAACAATGACTTACAAGGA CAGGGGATTCCCACCCACCTCCCCAGCTCCCATATTTCATGCCCAGCAACAATGACTTACAAGGA T A RAI1-AS1 Ensembl:ENSG00000237328 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17761721..17761956 26863196 MeRIP-seq:(Medium) rs1440924199 Functional Loss SNV dbSNP153 33..33 33 - - - 60297 RMVar_ID_60297 Human_SNP_ID_619102004 m1A Human chr17 - 17761728 17761728 17761728 CAGGGGATTCCCACCCACCTCCCCAGCTCCCAAATTTCATGCCCAGCAACAATGACTTACAAGGA CAGGGGATTCCCACCCACCTCCCCAGCTCCCAGATTTCATGCCCAGCAACAATGACTTACAAGGA T C RAI1-AS1 Ensembl:ENSG00000237328 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17761721..17761956 26863196 MeRIP-seq:(Medium) rs1440924199 Functional Loss SNV dbSNP153 33..33 33 - - - 60298 RMVar_ID_60298 Human_SNP_ID_619103145 m1A Human chr17 + 17766655 17766655 17766655 TGGATTCCCCAGCACTGCACTGTGCGAGGCCCAGGGCGGGGACCCCAGCAGGCAGCGTGGTAGGG TGGATTCCCCAGCACTGCACTGTGCGAGGCCCCGGGCGGGGACCCCAGCAGGCAGCGTGGTAGGG A C RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17766648..17767033 26863196 MeRIP-seq:(Medium) rs1320802986 Functional Loss SNV dbSNP153 33..33 33 - - - 60299 RMVar_ID_60299 Human_SNP_ID_619103782 m1A Human chr17 + 17769388 17769388 17769388 AGGCCTCCTTGGGACAGCCCGGGTCGGATCTCAGACTGCAGCATGTGGGGCTGGGAGCCAGCTCC AGGCCTCCTTGGGACAGCCCGGGTCGGATCTCGGACTGCAGCATGTGGGGCTGGGAGCCAGCTCC A G RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17769380..17769755 26863196 MeRIP-seq:(Medium) rs1368978701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542754,Human_RBP_ID_17206767 60300 RMVar_ID_60300 Human_SNP_ID_619110595 m1A Human chr17 + 17793275 17793275 17793275 GGCTACGGCGTCCAGGACAGCAGCCCCTACCCAGGCCGCTATGCTGGTGAGGAGAGCCTTCAGGC GGCTACGGCGTCCAGGACAGCAGCCCCTACCCGGGCCGCTATGCTGGTGAGGAGAGCCTTCAGGC A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17793069..17793470 32194978 MeRIP-seq:(Medium) rs750435058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526195 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60301 RMVar_ID_60301 Human_SNP_ID_619110684 m1A Human chr17 + 17793463 17793463 17793463 CGCCCAGGTGCCCTTTCGGACTCACTCCCTGCACGTCCAGCAGCCACCGCCGCCCCAGCAGCCCC CGCCCAGGTGCCCTTTCGGACTCACTCCCTGCGCGTCCAGCAGCCACCGCCGCCCCAGCAGCCCC A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17793412..17793592 26863196 MeRIP-seq:(Medium) rs767738169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27250387,Human_RBP_ID_27449045 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60302 RMVar_ID_60302 Human_SNP_ID_619110689 m1A Human chr17 + 17793469 17793469 17793469 GGTGCCCTTTCGGACTCACTCCCTGCACGTCCAGCAGCCACCGCCGCCCCAGCAGCCCCTGGCAT GGTGCCCTTTCGGACTCACTCCCTGCACGTCCGGCAGCCACCGCCGCCCCAGCAGCCCCTGGCAT A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17793419..17793701 26863196 MeRIP-seq:(Medium) rs1053199893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27449046 Human_Splice_Rec_1785737 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60303 RMVar_ID_60303 Human_SNP_ID_619111239 m1A Human chr17 - 17794628 17794628 17794628 GAGTCGTCAGATTTGGTGGACATGTCGTCAGGAGAGGTCACAGAACAGGTGGACACGGACTCGGG GAGTCGTCAGATTTGGTGGACATGTCGTCAGGGGAGGTCACAGAACAGGTGGACACGGACTCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17794579..17794710 26863196 MeRIP-seq:(Medium) rs1389509228 Functional Loss SNV dbSNP153 33..33 33 - - - 60304 RMVar_ID_60304 Human_SNP_ID_619111358 m1A Human chr17 + 17794900 17794900 17794900 CTTCTCGCTGGAGAACCACAGCGCCTGCCTGGACTCTGTGGCCAAGAGTGCGTGGCCCCGGCCTG CTTCTCGCTGGAGAACCACAGCGCCTGCCTGGTCTCTGTGGCCAAGAGTGCGTGGCCCCGGCCTG A T RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17794668..17796417 32194978 MeRIP-seq:(Medium) rs746654185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8813791,Human_RBP_ID_27449058 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60305 RMVar_ID_60305 Human_SNP_ID_619112000 m1A Human chr17 + 17796318 17796318 17796318 CCGCCCTGCCTGTGGCCTCCGACAGCAGCCCGATGGGCTCCAAGACCAAGGAGACAGACTCACCC CCGCCCTGCCTGTGGCCTCCGACAGCAGCCCGGTGGGCTCCAAGACCAAGGAGACAGACTCACCC A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17796268..17796430 26863196 MeRIP-seq:(Medium) rs764330506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60306 RMVar_ID_60306 Human_SNP_ID_619112125 m1A Human chr17 - 17796634 17796634 17796634 CCAGGTTCCGCTTCTTGGTGGGGACCGGCGCCATGAAGGCCGACTTCCTTTTGAGCGCATGGAGG CCAGGTTCCGCTTCTTGGTGGGGACCGGCGCCTTGAAGGCCGACTTCCTTTTGAGCGCATGGAGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17796587..17796682 26863196 MeRIP-seq:(Medium) rs369821666 Functional Loss SNV dbSNP153 33..33 33 - - - 60307 RMVar_ID_60307 Human_SNP_ID_619112126 m1A Human chr17 - 17796634 17796634 17796634 CCAGGTTCCGCTTCTTGGTGGGGACCGGCGCCATGAAGGCCGACTTCCTTTTGAGCGCATGGAGG CCAGGTTCCGCTTCTTGGTGGGGACCGGCGCCGTGAAGGCCGACTTCCTTTTGAGCGCATGGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17796587..17796682 26863196 MeRIP-seq:(Medium) rs369821666 Functional Loss SNV dbSNP153 33..33 33 - - - 60308 RMVar_ID_60308 Human_SNP_ID_619112664 m1A Human chr17 + 17797812 17797812 17797812 GCACTGTTGTCAACTCCCCTGGAGATGCGCCCAAGCCCCACAGGAAGCCTTCCTCCTCTGCCTCC GCACTGTTGTCAACTCCCCTGGAGATGCGCCCCAGCCCCACAGGAAGCCTTCCTCCTCTGCCTCC A C RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17797521..17797876 26863196 MeRIP-seq:(Medium) rs757056940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60309 RMVar_ID_60309 Human_SNP_ID_619112665 m1A Human chr17 + 17797812 17797812 17797812 GCACTGTTGTCAACTCCCCTGGAGATGCGCCCAAGCCCCACAGGAAGCCTTCCTCCTCTGCCTCC GCACTGTTGTCAACTCCCCTGGAGATGCGCCCGAGCCCCACAGGAAGCCTTCCTCCTCTGCCTCC A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17797521..17797876 26863196 MeRIP-seq:(Medium) rs757056940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60310 RMVar_ID_60310 Human_SNP_ID_619112666 m1A Human chr17 + 17797813 17797813 17797813 CACTGTTGTCAACTCCCCTGGAGATGCGCCCAAGCCCCACAGGAAGCCTTCCTCCTCTGCCTCCT CACTGTTGTCAACTCCCCTGGAGATGCGCCCAGGCCCCACAGGAAGCCTTCCTCCTCTGCCTCCT A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:17797551..17797875;chr17:17797584..17797950 26863196 MeRIP-seq:(Medium) rs745571330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 60311 RMVar_ID_60311 Human_SNP_ID_619112918 m1A Human chr17 - 17798363 17798363 17798363 CCGGGCTCTGCCGGAGCCTCCTTGCTGCACTCATGTTTGCGACCCTTGTCGGCTGGGGCTGCCTC CCGGGCTCTGCCGGAGCCTCCTTGCTGCACTCGTGTTTGCGACCCTTGTCGGCTGGGGCTGCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17798276..17798524 26863196 MeRIP-seq:(Medium) rs775376926 Functional Loss SNV dbSNP153 33..33 33 - - - 60312 RMVar_ID_60312 Human_SNP_ID_619116639 m1A Human chr17 + 17811074 17811074 17811074 ACTTGTCCACGCAGCCACCACCGGCCCGGGCCAGTCCCTGCCAGTCCGTCCGCCTGTCCGTCCGT ACTTGTCCACGCAGCCACCACCGGCCCGGGCCCGTCCCTGCCAGTCCGTCCGCCTGTCCGTCCGT A C RAI1 Ensembl:ENSG00000108557 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17811024..17811111 26863196 MeRIP-seq:(Medium) rs994114365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_471216,Human_miRNA_ID_477067,Human_miRNA_ID_939680 60313 RMVar_ID_60313 Human_SNP_ID_619116868 m1A Human chr17 - 17811592 17811592 17811592 GCCACACTGGAGAGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG GCCACACTGGAGAGGGGGCACAGGGGCGGGGGTGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG T A SREBF1 Ensembl:ENSG00000072310 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17811547..17811692 26863196 MeRIP-seq:(Medium) rs984197391 Functional Loss SNV dbSNP153 33..33 33 - - - 60314 RMVar_ID_60314 Human_SNP_ID_619116869 m1A Human chr17 - 17811592 17811592 17811592 GCCACACTGGAGAGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG GCCACACTGGAGAGGGGGCACAGGGGCGGGGGGGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG T C SREBF1 Ensembl:ENSG00000072310 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17811547..17811692 26863196 MeRIP-seq:(Medium) rs984197391 Functional Loss SNV dbSNP153 33..33 33 - - - 60315 RMVar_ID_60315 Human_SNP_ID_619116874 m1A Human chr17 - 17811612 17811611 17811612 CTCCTCCCTCCCGACCTGCCGCCACACTGGAGAGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTC CTCCTCCCTCCCGACCTGCCGCCACACTGGAG_GGGGGCACAGGGGCGGGGGAGGTTTCCTGTTC CT C SREBF1 Ensembl:ENSG00000072310 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17811561..17811727 26863196 MeRIP-seq:(Medium) rs1477079582 Functional Loss DEL dbSNP153 33..33 33 - - - 60316 RMVar_ID_60316 Human_SNP_ID_619116875 m1A Human chr17 - 17811612 17811612 17811612 CTCCTCCCTCCCGACCTGCCGCCACACTGGAGAGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTC CTCCTCCCTCCCGACCTGCCGCCACACTGGAGGGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTC T C SREBF1 Ensembl:ENSG00000072310 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17811561..17811727 26863196 MeRIP-seq:(Medium) rs899575088 Functional Loss SNV dbSNP153 33..33 33 - - - 60317 RMVar_ID_60317 Human_SNP_ID_619117279 m1A Human chr17 + 17812675 17812675 17812675 CCCACCGCCCAGGCGCATGAGCATCTGCTGACAGTCGTGCAGCAGCCGGCGATCGCCAAGCTTCT CCCACCGCCCAGGCGCATGAGCATCTGCTGACCGTCGTGCAGCAGCCGGCGATCGCCAAGCTTCT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:17812626..17812675 26863196 MeRIP-seq:(Medium) rs774907149 Functional Loss SNV dbSNP153 33..33 33 - - - 60318 RMVar_ID_60318 Human_SNP_ID_619117514 m1A Human chr17 + 17813282 17813282 17813282 TGCGCCAGGCCTGTCTGTCCCGTCTGACACACACACAGCCTCCCTTGGTATCACATCCCATGTGC TGCGCCAGGCCTGTCTGTCCCGTCTGACACACCCACAGCCTCCCTTGGTATCACATCCCATGTGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17813279..17813477 26863196 MeRIP-seq:(Medium) rs1417482959 Functional Loss SNV dbSNP153 33..33 33 - - - 60319 RMVar_ID_60319 Human_SNP_ID_619117515 m1A Human chr17 - 17813294 17813294 17813294 GCAGGGAAGGGCGCACATGGGATGTGATACCAAGGGAGGCTGTGTGTGTGTCAGACGGGACAGAC GCAGGGAAGGGCGCACATGGGATGTGATACCAGGGGAGGCTGTGTGTGTGTCAGACGGGACAGAC T C SREBF1 Ensembl:ENSG00000072310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17813290..17813428 26863196 MeRIP-seq:(Medium) rs1039416186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362566,Human_RBP_ID_22740856 60320 RMVar_ID_60320 Human_SNP_ID_619118645 m1A Human chr17 + 17816286 17816284 17816286 CAGCCGCCACATAGATCTCGGCCAGCGTCGCCACAGACACGGCATCCCCTGCACACTCTGCCAGG CAGCCGCCACATAGATCTCGGCCAGCGTCGC__CAGACACGGCATCCCCTGCACACTCTGCCAGG CCA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17815713..17816341 32194978 MeRIP-seq:(Medium) rs1424661602 Functional Loss DEL dbSNP153 32..33 33 - - - 60321 RMVar_ID_60321 Human_SNP_ID_619118827 m1A Human chr17 - 17816671 17816671 17816671 GCTGCCCAGCAGCTGTGGCTGGCCCTGCGGGCACTGGGCCGGCCCCTGCCCACCTCCCACCTGGA GCTGCCCAGCAGCTGTGGCTGGCCCTGCGGGCGCTGGGCCGGCCCCTGCCCACCTCCCACCTGGA T C SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:17816626..17816700 26863196 MeRIP-seq:(Medium) rs965777389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237514,Human_RBP_ID_18990618,Human_RBP_ID_22443484,Human_RBP_ID_27449135 Human_Splice_Rec_1785780,Human_Splice_Rec_1785816,Human_Splice_Rec_1785842,Human_Splice_Rec_1785874,Human_Splice_Rec_1785908,Human_Splice_Rec_1785946,Human_Splice_Rec_1785996,Human_Splice_Rec_1786006 RMVar_hsa_circ_8278 60322 RMVar_ID_60322 Human_SNP_ID_619119087 m1A Human chr17 - 17817361 17817361 17817361 TGTGCACGCTCGTCTTCCTCTGCCTGTCCTGCAACCCCTTGGCCTCCTTGCTGGGGGCCCGGGGG TGTGCACGCTCGTCTTCCTCTGCCTGTCCTGCGACCCCTTGGCCTCCTTGCTGGGGGCCCGGGGG T C SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17817312..17817486 26863196 MeRIP-seq:(Medium) rs1161491205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129082,Human_RBP_ID_27449138 Human_Splice_Rec_1785776,Human_Splice_Rec_1785812,Human_Splice_Rec_1785838,Human_Splice_Rec_1785870,Human_Splice_Rec_1785904,Human_Splice_Rec_1785942,Human_Splice_Rec_1786002,Human_Splice_Rec_1786008,Human_Splice_Rec_1786010 Human_miRNA_ID_167309,Human_miRNA_ID_729794,Human_miRNA_ID_970591,Human_miRNA_ID_1035641 RMVar_hsa_circ_8278,RMVar_hsa_circ_32721 60323 RMVar_ID_60323 Human_SNP_ID_619119251 m1A Human chr17 - 17817703 17817703 17817703 TGACTCGGAGCCTGACAGCCCAGTCTTTGAGGACAGCAAGGTTGGGCCCTGCCACGGTGCCCCCT TGACTCGGAGCCTGACAGCCCAGTCTTTGAGGGCAGCAAGGTTGGGCCCTGCCACGGTGCCCCCT T C SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:17817701..17817725 26863196 MeRIP-seq:(Medium) rs1451680345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277963,Human_RBP_ID_896258,Human_RBP_ID_2496006,Human_RBP_ID_3951901,Human_RBP_ID_22061062 Human_Splice_Rec_1785775,Human_Splice_Rec_1785811,Human_Splice_Rec_1785869,Human_Splice_Rec_1785901,Human_Splice_Rec_1785941,Human_Splice_Rec_1785999,Human_Splice_Rec_1786007,Human_Splice_Rec_1786009 RMVar_hsa_circ_8278,RMVar_hsa_circ_32721,RMVar_hsa_circ_34315 60324 RMVar_ID_60324 Human_SNP_ID_619119904 m1A Human chr17 + 17819675 17819675 17819675 GTGCAAGGAGACGGGCGGGACCCCTGGCGGGGAAGCCAGTGGCAGGCCAGGCAGCGGCTGCTGGG GTGCAAGGAGACGGGCGGGACCCCTGGCGGGGGAGCCAGTGGCAGGCCAGGCAGCGGCTGCTGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17819544..17819944 32194978 MeRIP-seq:(Medium) rs1392086268 Functional Loss SNV dbSNP153 33..33 33 - - - 60325 RMVar_ID_60325 Human_SNP_ID_619120062 m1A Human chr17 - 17820175 17820175 17820175 ACCCCACAGCCCCTGCCAGGGGCCCTCCTGCCACAGAGCTTCCCAGCCCCAGCCCCACCGCAGTT ACCCCACAGCCCCTGCCAGGGGCCCTCCTGCCGCAGAGCTTCCCAGCCCCAGCCCCACCGCAGTT T C SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:17820151..17820350 26863196 MeRIP-seq:(Medium) rs757230938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129489,Human_RBP_ID_17079994,Human_RBP_ID_18942912 Human_Splice_Rec_1785765,Human_Splice_Rec_1785801,Human_Splice_Rec_1785931,Human_Splice_Rec_1786017 RMVar_hsa_circ_8278 60326 RMVar_ID_60326 Human_SNP_ID_619120109 m1A Human chr17 + 17820294 17820294 17820294 GGAGAAAGCGGGCATGGACGGGTACATCTTCAATGGAGTGGGTGCAGGCTGGGGAGGGGACAGGG GGAGAAAGCGGGCATGGACGGGTACATCTTCAGTGGAGTGGGTGCAGGCTGGGGAGGGGACAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr17:17820086..17820543;chr17:17820093..17820543 26863196,32194978 MeRIP-seq:(Medium) rs760938572 Functional Loss SNV dbSNP153 33..33 33 - - - 60327 RMVar_ID_60327 Human_SNP_ID_619120138 m1A Human chr17 - 17820375 17820375 17820375 CAGGCAGCTTGTCTCCACCTCCTGCCACATTGAGCTCCTCTCTTGAAGCCTTCCTGAGCGGGCCG CAGGCAGCTTGTCTCCACCTCCTGCCACATTGTGCTCCTCTCTTGAAGCCTTCCTGAGCGGGCCG T A SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:17820226..17820500 32194978 MeRIP-seq:(Medium) rs1407488218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50286,Human_RBP_ID_8445690,Human_RBP_ID_17079995,Human_RBP_ID_18942916 Human_Splice_Rec_1786029 RMVar_hsa_circ_8278 60328 RMVar_ID_60328 Human_SNP_ID_619120155 m1A Human chr17 + 17820396 17820396 17820396 AAGAGAGGAGCTCAATGTGGCAGGAGGTGGAGACAAGCTGCCTGGGGAGCTGGTATCGGGGCTGG AAGAGAGGAGCTCAATGTGGCAGGAGGTGGAGCCAAGCTGCCTGGGGAGCTGGTATCGGGGCTGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:17820101..17820525 26863196 MeRIP-seq:(Medium) rs1224442476 Functional Loss SNV dbSNP153 33..33 33 - - - 60329 RMVar_ID_60329 Human_SNP_ID_619120846 m1A Human chr17 - 17823484 17823484 17823484 TATTTTTGGAGGCCTCCCCACCAGCCCTTTATACAATGCCTCCGTCTCCTGCAGGTTCTCCTGGG TATTTTTGGAGGCCTCCCCACCAGCCCTTTATGCAATGCCTCCGTCTCCTGCAGGTTCTCCTGGG T C SREBF1 Ensembl:ENSG00000072310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17823481..17823596 26863196 MeRIP-seq:(Medium) rs776200304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541585,Human_RBP_ID_8092589 RMVar_hsa_circ_8278 60330 RMVar_ID_60330 Human_SNP_ID_619120851 m1A Human chr17 - 17823497 17823497 17823497 GCACTTTCGAAGGTATTTTTGGAGGCCTCCCCACCAGCCCTTTATACAATGCCTCCGTCTCCTGC GCACTTTCGAAGGTATTTTTGGAGGCCTCCCCGCCAGCCCTTTATACAATGCCTCCGTCTCCTGC T C SREBF1 Ensembl:ENSG00000072310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17823495..17823600 26863196 MeRIP-seq:(Medium) rs764602703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541585 RMVar_hsa_circ_8278 60331 RMVar_ID_60331 Human_SNP_ID_619127056 m1A Human chr17 + 17847523 17847523 17847523 GCCTGGGAGCAGACACGGTGGCATTTCCATGGAAACACAGGTGTGCAGGCCGTGTGGAGCTGGGG GCCTGGGAGCAGACACGGTGGCATTTCCATGGGAACACAGGTGTGCAGGCCGTGTGGAGCTGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17847476..17847652 26863196 MeRIP-seq:(Medium) rs377155114 Functional Loss SNV dbSNP153 33..33 33 - - - 60332 RMVar_ID_60332 Human_SNP_ID_619127073 m1A Human chr17 - 17847579 17847579 17847579 AGATGGCGGGTCCCCGCTCGCACCCCGTGGACACCGGGCACTGGCCACTCCTACATCCCCAGCTC AGATGGCGGGTCCCCGCTCGCACCCCGTGGACGCCGGGCACTGGCCACTCCTACATCCCCAGCTC T C TOM1L2 Ensembl:ENSG00000175662 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:17847536..17847692 26863196 MeRIP-seq:(Medium) rs149458835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27449164 60333 RMVar_ID_60333 Human_SNP_ID_619137962 m1A Human chr17 - 17893201 17893201 17893201 TGGACCCTGAAGAATGATGGGGAGTTTGGTGGAAAAGTCAGTGGGAGAGACTTCACAGGCAGGGA TGGACCCTGAAGAATGATGGGGAGTTTGGTGGGAAAGTCAGTGGGAGAGACTTCACAGGCAGGGA T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17893193..17893327 26863196 MeRIP-seq:(Medium) rs900390991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94606,RMVar_hsa_circ_366018,RMVar_hsa_circ_365847,RMVar_hsa_circ_182411,RMVar_hsa_circ_304575,RMVar_hsa_circ_328430,RMVar_hsa_circ_28079,RMVar_hsa_circ_182418,RMVar_hsa_circ_290216,RMVar_hsa_circ_319613,RMVar_hsa_circ_182419,RMVar_hsa_circ_182420,RMVar_hsa_circ_333292,RMVar_hsa_circ_348559,RMVar_hsa_circ_314848 60334 RMVar_ID_60334 Human_SNP_ID_619141410 m1A Human chr17 - 17907528 17907527 17907528 GTAAACCCATTTTCTCTCTGATTTCACAGAAAAGGCAACAGATGGCTCCCTGCAAAGTGAGGATT GTAAACCCATTTTCTCTCTGATTTCACAGAAA_GGCAACAGATGGCTCCCTGCAAAGTGAGGATT CT C TOM1L2 Ensembl:ENSG00000175662 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17907492..17907581 26863196 MeRIP-seq:(Medium) rs1325539407 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1786038,Human_Splice_Rec_1786039,Human_Splice_Rec_1786080,Human_Splice_Rec_1786081,Human_Splice_Rec_1786108,Human_Splice_Rec_1786109,Human_Splice_Rec_1786136,Human_Splice_Rec_1786137,Human_Splice_Rec_1786162,Human_Splice_Rec_1786163,Human_Splice_Rec_1786190,Human_Splice_Rec_1786191,Human_Splice_Rec_1786216,Human_Splice_Rec_1786217,Human_Splice_Rec_1786250,Human_Splice_Rec_1786251,Human_Splice_Rec_1786263 RMVar_hsa_circ_94606,RMVar_hsa_circ_182411,RMVar_hsa_circ_304575,RMVar_hsa_circ_28079,RMVar_hsa_circ_290216,RMVar_hsa_circ_182419,RMVar_hsa_circ_333292,RMVar_hsa_circ_305518,RMVar_hsa_circ_182422,RMVar_hsa_circ_266551 60335 RMVar_ID_60335 Human_SNP_ID_619145939 m1A Human chr17 - 17924998 17924994 17924999 AGAGAGTGGAGGAGGGAGTGCCACACACTTTTAACTGACCAGATATTGCAAGAATTATCACAAAG AGAGAGTGGAGGAGGGAGTGCCACACACTTT_____GACCAGATATTGCAAGAATTATCACAAAG CAGTTA C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17924994..17925101 26863196 MeRIP-seq:(Medium) rs910894056 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_266551 60336 RMVar_ID_60336 Human_SNP_ID_619173436 m1A Human chr17 + 18039118 18039118 18039118 AGCCGCACGGTCGGGCTGTACGGAAACCTCTCAACGCCTCCTCAGAGCCCTCAACCTCCCTTGGA AGCCGCACGGTCGGGCTGTACGGAAACCTCTCGACGCCTCCTCAGAGCCCTCAACCTCCCTTGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18039036..18039151 26863196 MeRIP-seq:(Medium) rs935451546 Functional Loss SNV dbSNP153 33..33 33 - - - 60337 RMVar_ID_60337 Human_SNP_ID_619173439 m1A Human chr17 - 18039124 18039124 18039124 GCGGCGTCCAAGGGAGGTTGAGGGCTCTGAGGAGGCGTTGAGAGGTTTCCGTACAGCCCGACCGT GCGGCGTCCAAGGGAGGTTGAGGGCTCTGAGGCGGCGTTGAGAGGTTTCCGTACAGCCCGACCGT T G ATPAF2 Ensembl:ENSG00000171953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:18039041..18039128;chr17:18039046..18039142 26863196 MeRIP-seq:(Medium) rs1294192156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896276,Human_RBP_ID_18419900,Human_RBP_ID_18438464,Human_RBP_ID_19081679 60338 RMVar_ID_60338 Human_SNP_ID_619173607 m1A Human chr17 - 18039537 18039537 18039537 CCTGCGGAGCAAGCGCTCCGGCCGCCACCGGGACCCAGGGACCTGCGAGCAGGGCCTCCCAGTCC CCTGCGGAGCAAGCGCTCCGGCCGCCACCGGGGCCCAGGGACCTGCGAGCAGGGCCTCCCAGTCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:18039439..18039766 26863196 MeRIP-seq:(Medium) rs1459836808 Functional Loss SNV dbSNP153 33..33 33 - - - 60339 RMVar_ID_60339 Human_SNP_ID_619173671 m1A Human chr17 - 18039651 18039651 18039651 GAGTGGGAGAGGAACCGCCGCCGCCGCGCGGGAGCCGAGGAGGGTGGCGGGGAGGGAGAGGCCGG GAGTGGGAGAGGAACCGCCGCCGCCGCGCGGGGGCCGAGGAGGGTGGCGGGGAGGGAGAGGCCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:18039559..18039749 26863410 MeRIP-seq:(Medium) rs1267548943 Functional Loss SNV dbSNP153 33..33 33 - - - 60340 RMVar_ID_60340 Human_SNP_ID_619173702 m1A Human chr17 - 18039694 18039694 18039694 TGCGGACCGGCATCGCGGGGTCCCCCGGAGCCAGGGCTGGGGGGAGTGGGAGAGGAACCGCCGCC TGCGGACCGGCATCGCGGGGTCCCCCGGAGCCGGGGCTGGGGGGAGTGGGAGAGGAACCGCCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18039647..18039810 26863196 MeRIP-seq:(Medium) rs747481250 Functional Loss SNV dbSNP153 33..33 33 - - - 60341 RMVar_ID_60341 Human_SNP_ID_619173704 m1A Human chr17 - 18039698 18039698 18039698 TCGGTGCGGACCGGCATCGCGGGGTCCCCCGGAGCCAGGGCTGGGGGGAGTGGGAGAGGAACCGC TCGGTGCGGACCGGCATCGCGGGGTCCCCCGGCGCCAGGGCTGGGGGGAGTGGGAGAGGAACCGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,Wild Type;HEPG2 cell line,mRNA untreated chr17:18039602..18039775;chr17:18039649..18039845 26863410,26863196 MeRIP-seq:(Medium) rs1313953306 Functional Loss SNV dbSNP153 33..33 33 - - - 60342 RMVar_ID_60342 Human_SNP_ID_619173733 m1A Human chr17 - 18039758 18039758 18039758 GGCGGCGGCGGGATGAGTGAGGCCGCGGAGGCAGCGGAGGCACCGGCCGGCGGGGGACACTCGGT GGCGGCGGCGGGATGAGTGAGGCCGCGGAGGCTGCGGAGGCACCGGCCGGCGGGGGACACTCGGT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18039708..18039804 26863196 MeRIP-seq:(Medium) rs767387883 Functional Loss SNV dbSNP153 33..33 33 - - - 60343 RMVar_ID_60343 Human_SNP_ID_619173734 m1A Human chr17 - 18039758 18039758 18039758 GGCGGCGGCGGGATGAGTGAGGCCGCGGAGGCAGCGGAGGCACCGGCCGGCGGGGGACACTCGGT GGCGGCGGCGGGATGAGTGAGGCCGCGGAGGCCGCGGAGGCACCGGCCGGCGGGGGACACTCGGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18039708..18039804 26863196 MeRIP-seq:(Medium) rs767387883 Functional Loss SNV dbSNP153 33..33 33 - - - 60344 RMVar_ID_60344 Human_SNP_ID_619180285 m1A Human chr17 + 18067138 18067138 18067138 TGAGCTGATGGCCTTGGTTGAGCTGATGGACAAGTGAAGGAGGCCATGGGGCTGTGCTGTCCTTC TGAGCTGATGGCCTTGGTTGAGCTGATGGACAGGTGAAGGAGGCCATGGGGCTGTGCTGTCCTTC A G GID4 Ensembl:ENSG00000141034 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18067087..18067165 26863196 MeRIP-seq:(Medium) rs1191745732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484353,Human_RBP_ID_8445819 Human_miRNA_ID_548238 60345 RMVar_ID_60345 Human_SNP_ID_619180309 m1A Human chr17 - 18067202 18067200 18067202 GAAGGTATGGGCTCGCATGCTGTTGAGGGGAGAGCTGAAGAGAGTGGAATGGCACGTACGGCAGG GAAGGTATGGGCTCGCATGCTGTTGAGGGGAG__CTGAAGAGAGTGGAATGGCACGTACGGCAGG GCT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18067151..18067400 32194978 MeRIP-seq:(Medium) rs952029057 Functional Loss DEL dbSNP153 33..34 33 - - - 60346 RMVar_ID_60346 Human_SNP_ID_619180310 m1A Human chr17 - 18067202 18067202 18067202 GAAGGTATGGGCTCGCATGCTGTTGAGGGGAGAGCTGAAGAGAGTGGAATGGCACGTACGGCAGG GAAGGTATGGGCTCGCATGCTGTTGAGGGGAGGGCTGAAGAGAGTGGAATGGCACGTACGGCAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18067151..18067400 32194978 MeRIP-seq:(Medium) rs984680870 Functional Loss SNV dbSNP153 33..33 33 - - - 60347 RMVar_ID_60347 Human_SNP_ID_619185684 m1A Human chr17 - 18088002 18088002 18088002 AAGATCCCCATGGTAGCAGCAGAGGTGGGCGCACAGACAGCGGTGGCGGCGGCACCGGCAATTCC AAGATCCCCATGGTAGCAGCAGAGGTGGGCGCGCAGACAGCGGTGGCGGCGGCACCGGCAATTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:18087951..18088143;chr17:18087951..18088128;chr17:18087951..18088069 26863196 MeRIP-seq:(Medium) rs1260170258 Functional Loss SNV dbSNP153 33..33 33 - - - 60348 RMVar_ID_60348 Human_SNP_ID_619188812 m1A Human chr17 - 18100357 18100357 18100357 GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGAAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGTAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18100351..18100450 32194978 MeRIP-seq:(Medium) rs2272570 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7263,GWAS_ID_7264,GWAS_ID_7265,GWAS_ID_7266,GWAS_ID_7267,GWAS_ID_7268,GWAS_ID_7269,GWAS_ID_7270,GWAS_ID_7271,GWAS_ID_7272,GWAS_ID_7273,GWAS_ID_7274,GWAS_ID_7275,GWAS_ID_7276,GWAS_ID_7277,GWAS_ID_7278,GWAS_ID_7279,GWAS_ID_7280,GWAS_ID_7281,GWAS_ID_7282,GWAS_ID_7283,GWAS_ID_7284,GWAS_ID_7285,GWAS_ID_7286,GWAS_ID_7287,GWAS_ID_7288,GWAS_ID_7289,GWAS_ID_7290,GWAS_ID_7291,GWAS_ID_7292,GWAS_ID_7293,GWAS_ID_7294,GWAS_ID_7295,GWAS_ID_7296 60349 RMVar_ID_60349 Human_SNP_ID_619188813 m1A Human chr17 - 18100357 18100357 18100357 GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGAAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGCAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18100351..18100450 32194978 MeRIP-seq:(Medium) rs2272570 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7263,GWAS_ID_7264,GWAS_ID_7265,GWAS_ID_7266,GWAS_ID_7267,GWAS_ID_7268,GWAS_ID_7269,GWAS_ID_7270,GWAS_ID_7271,GWAS_ID_7272,GWAS_ID_7273,GWAS_ID_7274,GWAS_ID_7275,GWAS_ID_7276,GWAS_ID_7277,GWAS_ID_7278,GWAS_ID_7279,GWAS_ID_7280,GWAS_ID_7281,GWAS_ID_7282,GWAS_ID_7283,GWAS_ID_7284,GWAS_ID_7285,GWAS_ID_7286,GWAS_ID_7287,GWAS_ID_7288,GWAS_ID_7289,GWAS_ID_7290,GWAS_ID_7291,GWAS_ID_7292,GWAS_ID_7293,GWAS_ID_7294,GWAS_ID_7295,GWAS_ID_7296 60350 RMVar_ID_60350 Human_SNP_ID_619190803 m1A Human chr17 - 18107871 18107869 18107871 TAAACTCAAAAGTCCCTGCCCCAGGCGTGCAGAGCCAGGGTCCTGGGGTTTTGTGCTGGGCAGGG TAAACTCAAAAGTCCCTGCCCCAGGCGTGCAG__CCAGGGTCCTGGGGTTTTGTGCTGGGCAGGG GCT G AC087164.2 Ensembl:ENSG00000279428 Other exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18107821..18107921 32194978 MeRIP-seq:(Medium) rs1201781359 Functional Loss DEL dbSNP153 33..34 33 - - - 60351 RMVar_ID_60351 Human_SNP_ID_619212431 m1A Human chr17 + 18184014 18184014 18184014 TGCCGGCGCCCCTGCCCCGCGGGACGTGGAGAAGGTGGAGGAGGAAGAAGCCCCGTTGTCGCCAC TGCCGGCGCCCCTGCCCCGCGGGACGTGGAGACGGTGGAGGAGGAAGAAGCCCCGTTGTCGCCAC A C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:18183851..18184100 26863196 MeRIP-seq:(Medium) rs1256860570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235751,Human_RBP_ID_1528952,Human_RBP_ID_4466140,Human_RBP_ID_18690733 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60352 RMVar_ID_60352 Human_SNP_ID_619212614 m1A Human chr17 + 18184372 18184333 18184372 GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCAGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC _________________________________GCCGCCGCTGCCGCCGAACCTTACCCTGTGTC CGCCGCCGCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCA C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18184276..18184450 26863410 MeRIP-seq:(Medium) rs1567672804 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4466145,Human_RBP_ID_6565976,Human_RBP_ID_17886445 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60353 RMVar_ID_60353 Human_SNP_ID_619212651 m1A Human chr17 + 18184372 18184360 18184372 GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCAGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC GCTGCCGCAGCCGCCGTAGCC____________GCCGCCGCTGCCGCCGAACCTTACCCTGTGTC CGCCGCAGCCGCA C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18184276..18184450 26863410 MeRIP-seq:(Medium) rs771220641 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4466145,Human_RBP_ID_6565976,Human_RBP_ID_17886445 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60354 RMVar_ID_60354 Human_SNP_ID_619212652 m1A Human chr17 + 18184372 18184360 18184372 GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCAGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC GCTGCCGCAGCCGCCGTAGCCGCCGCA______GCCGCCGCTGCCGCCGAACCTTACCCTGTGTC CGCCGCAGCCGCA CGCCGCA ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18184276..18184450 26863410 MeRIP-seq:(Medium) rs771220641 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4466145,Human_RBP_ID_6565976,Human_RBP_ID_17886445 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60355 RMVar_ID_60355 Human_SNP_ID_619212656 m1A Human chr17 + 18184372 18184363 18184372 GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCAGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC GCTGCCGCAGCCGCCGTAGCCGCC_________GCCGCCGCTGCCGCCGAACCTTACCCTGTGTC CGCAGCCGCA C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18184276..18184450 26863410 MeRIP-seq:(Medium) rs1567672851 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4466145,Human_RBP_ID_6565976,Human_RBP_ID_17886445 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60356 RMVar_ID_60356 Human_SNP_ID_619212666 m1A Human chr17 + 18184372 18184372 18184372 GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCAGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC GCTGCCGCAGCCGCCGTAGCCGCCGCAGCCGCCGCCGCCGCTGCCGCCGAACCTTACCCTGTGTC A C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18184276..18184450 26863410 MeRIP-seq:(Medium) rs1029992487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466145,Human_RBP_ID_6565976,Human_RBP_ID_17886445 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 60357 RMVar_ID_60357 Human_SNP_ID_619219717 m1A Human chr17 + 18209050 18209050 18209050 AGCCCCCCAGGCGTCCTCCACCCACGCCCACTAGCCTGCCATGTCCACAGTTCCTTGGGCTGCTG AGCCCCCCAGGCGTCCTCCACCCACGCCCACTGGCCTGCCATGTCCACAGTTCCTTGGGCTGCTG A G ALKBH5 Ensembl:ENSG00000091542 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18209001..18209100 32194978 MeRIP-seq:(Medium) rs1341935112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484463,Human_RBP_ID_6566149,Human_RBP_ID_8191815,Human_RBP_ID_8445915,Human_RBP_ID_18178895,Human_RBP_ID_22803368,Human_RBP_ID_23714344 RMVar_hsa_circ_76382,RMVar_hsa_circ_182436,RMVar_hsa_circ_109858,RMVar_hsa_circ_78791,RMVar_hsa_circ_182439,RMVar_hsa_circ_182440 60358 RMVar_ID_60358 Human_SNP_ID_619224285 m1A Human chr17 + 18225717 18225717 18225717 GATGAAGTTTCGGTTCCGGCGGCAGGGCGCCGACCCGCAGCGCGAGAAGCTCAAGCAGGAGCTTT GATGAAGTTTCGGTTCCGGCGGCAGGGCGCCGGCCCGCAGCGCGAGAAGCTCAAGCAGGAGCTTT A G LLGL1 Ensembl:ENSG00000131899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18225670..18225795 26863196 MeRIP-seq:(Medium) rs1383002095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464374,Human_RBP_ID_23714368 Human_Splice_Rec_1787445,Human_Splice_Rec_1787489 RMVar_hsa_circ_78535,RMVar_hsa_circ_95526,RMVar_hsa_circ_182441,RMVar_hsa_circ_182442 60359 RMVar_ID_60359 Human_SNP_ID_619224414 m1A Human chr17 - 18226041 18226041 18226041 ACCCAGAGACAGGCAAAGAGTCTCAGAGACAGACCCCCACACACACAGACTGGCAGAGCCAGGGC ACCCAGAGACAGGCAAAGAGTCTCAGAGACAGGCCCCCACACACACAGACTGGCAGAGCCAGGGC T C lnc-TOP3A-1 RNACentral:URS0000D59144 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18226035..18226155 32194978 MeRIP-seq:(Medium) rs1340979141 Functional Loss SNV dbSNP153 33..33 33 - - - 60360 RMVar_ID_60360 Human_SNP_ID_619224753 m1A Human chr17 + 18227204 18227204 18227204 GGTTTCCCTGCCTAGGTCTGCAGTGATTGCCGATGAGAGCTGCCAGGACCCTCACACGGTGGCTG GGTTTCCCTGCCTAGGTCTGCAGTGATTGCCGGTGAGAGCTGCCAGGACCCTCACACGGTGGCTG A G LLGL1 Ensembl:ENSG00000131899 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18227199..18227315 32194978 MeRIP-seq:(Medium) rs1007528951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12913687 RMVar_hsa_circ_78535,RMVar_hsa_circ_95526,RMVar_hsa_circ_182441,RMVar_hsa_circ_182442 60361 RMVar_ID_60361 Human_SNP_ID_619226114 m1A Human chr17 + 18232520 18232520 18232520 CCCTCAGCTATGGTGCACCTGGCGTGGAGTTCACAGGCCTGCACCGGGATGCAGCCACTGTCACA CCCTCAGCTATGGTGCACCTGGCGTGGAGTTCGCAGGCCTGCACCGGGATGCAGCCACTGTCACA A G LLGL1 Ensembl:ENSG00000131899 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18230013..18232569 32194978 MeRIP-seq:(Medium) rs1219582722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4409459 Human_Splice_Rec_1787448,Human_Splice_Rec_1787449,Human_Splice_Rec_1787492,Human_Splice_Rec_1787493 Human_miRNA_ID_2421959 RMVar_hsa_circ_28410,RMVar_hsa_circ_78535,RMVar_hsa_circ_95526,RMVar_hsa_circ_182441,RMVar_hsa_circ_182442,RMVar_hsa_circ_62804,RMVar_hsa_circ_182443,RMVar_hsa_circ_100495 60362 RMVar_ID_60362 Human_SNP_ID_619227741 m1A Human chr17 + 18237023 18237023 18237023 GAGATGAGCTGGAGGGTCTGGTGGAAAGGGAGATGGACTGGCACAGGCAAAAGCCAAGGTGGGAA GAGATGAGCTGGAGGGTCTGGTGGAAAGGGAGGTGGACTGGCACAGGCAAAAGCCAAGGTGGGAA A G LLGL1 Ensembl:ENSG00000131899 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18236973..18237067 26863196 MeRIP-seq:(Medium) rs756739981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5363842,Human_RBP_ID_19078487 RMVar_hsa_circ_85723,RMVar_hsa_circ_28410,RMVar_hsa_circ_78535,RMVar_hsa_circ_95526,RMVar_hsa_circ_182441,RMVar_hsa_circ_182442,RMVar_hsa_circ_93514,RMVar_hsa_circ_182443,RMVar_hsa_circ_100495,RMVar_hsa_circ_182445,RMVar_hsa_circ_96029,RMVar_hsa_circ_92553,RMVar_hsa_circ_111864,RMVar_hsa_circ_182448,RMVar_hsa_circ_182450,RMVar_hsa_circ_107858,RMVar_hsa_circ_182449,RMVar_hsa_circ_77016,RMVar_hsa_circ_78074,RMVar_hsa_circ_182451,RMVar_hsa_circ_182452,RMVar_hsa_circ_112009,RMVar_hsa_circ_182453,RMVar_hsa_circ_182454,RMVar_hsa_circ_182456 60363 RMVar_ID_60363 Human_SNP_ID_619227853 m1A Human chr17 - 18237462 18237461 18237462 TCCAGTACCAGCACCTGAGCCCACAGCCAGGCAGGGGGAGCATCAGCGCAGGGGAGGGGCCGCCC TCCAGTACCAGCACCTGAGCCCACAGCCAGGC_GGGGGAGCATCAGCGCAGGGGAGGGGCCGCCC CT C lnc-TOP3A-1 RNACentral:URS0000D59144 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18237457..18238079 32194978 MeRIP-seq:(Medium) rs1158984748 Functional Loss DEL dbSNP153 33..33 33 - - - 60364 RMVar_ID_60364 Human_SNP_ID_619227856 m1A Human chr17 - 18237462 18237462 18237462 TCCAGTACCAGCACCTGAGCCCACAGCCAGGCAGGGGGAGCATCAGCGCAGGGGAGGGGCCGCCC TCCAGTACCAGCACCTGAGCCCACAGCCAGGCCGGGGGAGCATCAGCGCAGGGGAGGGGCCGCCC T G lnc-TOP3A-1 RNACentral:URS0000D59144 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18237457..18238079 32194978 MeRIP-seq:(Medium) rs1441492929 Functional Loss SNV dbSNP153 33..33 33 - - - 60365 RMVar_ID_60365 Human_SNP_ID_619229012 m1A Human chr17 - 18240858 18240858 18240858 AGCCCACAGTGGCTCACCTTGAACTGCTCCTCAGATGCGATGAGCACAGCGTGACCACCCTGCAT AGCCCACAGTGGCTCACCTTGAACTGCTCCTCGGATGCGATGAGCACAGCGTGACCACCCTGCAT T C lnc-TOP3A-1 RNACentral:URS0000D59144 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18240586..18240875 32194978 MeRIP-seq:(Medium) rs76973089 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 60366 RMVar_ID_60366 Human_SNP_ID_619230803 m1A Human chr17 + 18245406 18245406 18245406 GCTTGATCTCCACCTGGCTAGTCTGGGTCCCCACCCACATGTAGACCTGTGGGGGCAGCAGGGGA GCTTGATCTCCACCTGGCTAGTCTGGGTCCCCGCCCACATGTAGACCTGTGGGGGCAGCAGGGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18245336..18245427 26863196 MeRIP-seq:(Medium) rs146460796 Functional Loss SNV dbSNP153 33..33 33 - - - 60367 RMVar_ID_60367 Human_SNP_ID_619230986 m1A Human chr17 - 18245766 18245766 18245766 CACAGAAGCCCTATGATGACGATGCCGAGTACATGAAACACACACGTCTCTTCCGGTGAGGCCAG CACAGAAGCCCTATGATGACGATGCCGAGTACGTGAAACACACACGTCTCTTCCGGTGAGGCCAG T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18245738..18246022 26863196 MeRIP-seq:(Medium) rs773852769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22947554 Human_Splice_Rec_1787608,Human_Splice_Rec_1787609,Human_Splice_Rec_1787622,Human_Splice_Rec_1787623,Human_Splice_Rec_1787708,Human_Splice_Rec_1787709,Human_Splice_Rec_1787766,Human_Splice_Rec_1787767,Human_Splice_Rec_1787824,Human_Splice_Rec_1787825,Human_Splice_Rec_1787841,Human_Splice_Rec_1787846,Human_Splice_Rec_1787847,Human_Splice_Rec_1787854,Human_Splice_Rec_1787855,Human_Splice_Rec_1787866,Human_Splice_Rec_1787867 RMVar_hsa_circ_76013,RMVar_hsa_circ_118444,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182464,RMVar_hsa_circ_182465,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_369743,RMVar_hsa_circ_182470,RMVar_hsa_circ_182471 60368 RMVar_ID_60368 Human_SNP_ID_619231204 m1A Human chr17 + 18246154 18246142 18246155 CCTTGGTCCACGGAGTCCTGGCTCACACCCACAACCCCACCTTGAGGATGAAGCAGAACTCGGAG CCTTGGTCCACGGAGTCCTGG_____________CCCCACCTTGAGGATGAAGCAGAACTCGGAG GCTCACACCCACAA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18246151..18246275 32194978 MeRIP-seq:(Medium) rs750528799 Functional Loss DEL dbSNP153 22..34 33 - - - 60369 RMVar_ID_60369 Human_SNP_ID_619231212 m1A Human chr17 + 18246154 18246154 18246154 CCTTGGTCCACGGAGTCCTGGCTCACACCCACAACCCCACCTTGAGGATGAAGCAGAACTCGGAG CCTTGGTCCACGGAGTCCTGGCTCACACCCACCACCCCACCTTGAGGATGAAGCAGAACTCGGAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18246151..18246275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 60370 RMVar_ID_60370 Human_SNP_ID_619231437 m1A Human chr17 - 18246626 18246623 18246626 GCTGGCTCACCTTCACCTTCAGCCTGCAAAAGAAGTTCGAGAGCCTCTTCCCTGGGAAGCTGGAG GCTGGCTCACCTTCACCTTCAGCCTGCAAAAG___TTCGAGAGCCTCTTCCCTGGGAAGCTGGAG ACTT A FLII Ensembl:ENSG00000177731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18246576..18246625 32194978 MeRIP-seq:(Medium) rs879568374 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_22444397,Human_RBP_ID_27813503 Human_Splice_Rec_1787601,Human_Splice_Rec_1787701,Human_Splice_Rec_1787759,Human_Splice_Rec_1787817,Human_Splice_Rec_1787877,Human_Splice_Rec_1787881 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60371 RMVar_ID_60371 Human_SNP_ID_619231492 m1A Human chr17 - 18246751 18246751 18246751 CAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGAGGAAGCAACCGCTGAGGCAGAGGAGAAGCAGC CAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGGGGAAGCAACCGCTGAGGCAGAGGAGAAGCAGC T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18246576..18246850 26863196 MeRIP-seq:(Medium) rs201095894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766356,Human_RBP_ID_903438,Human_RBP_ID_26331375,Human_RBP_ID_27812365 Human_Splice_Rec_1787600,Human_Splice_Rec_1787700,Human_Splice_Rec_1787758,Human_Splice_Rec_1787816,Human_Splice_Rec_1787880,Human_Splice_Rec_1787888 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60372 RMVar_ID_60372 Human_SNP_ID_619231500 m1A Human chr17 - 18246766 18246766 18246766 GGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGAGGAAGCAACCGCTGAGG GGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGGGGGCAAAGAAGGCGAGGAAGCAACCGCTGAGG T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr17:18246651..18246975;chr17:18246686..18246850 26863196 MeRIP-seq:(Medium) rs200248186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903438,Human_RBP_ID_26331375,Human_RBP_ID_27812365 Human_Splice_Rec_1787600,Human_Splice_Rec_1787700,Human_Splice_Rec_1787758,Human_Splice_Rec_1787816,Human_Splice_Rec_1787880,Human_Splice_Rec_1787888 Human_miRNA_ID_209706 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60373 RMVar_ID_60373 Human_SNP_ID_619231501 m1A Human chr17 - 18246766 18246766 18246766 GGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGAGGAAGCAACCGCTGAGG GGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGCGGGCAAAGAAGGCGAGGAAGCAACCGCTGAGG T G FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr17:18246651..18246975;chr17:18246686..18246850 26863196 MeRIP-seq:(Medium) rs200248186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903438,Human_RBP_ID_26331375,Human_RBP_ID_27812365 Human_Splice_Rec_1787600,Human_Splice_Rec_1787700,Human_Splice_Rec_1787758,Human_Splice_Rec_1787816,Human_Splice_Rec_1787880,Human_Splice_Rec_1787888 Human_miRNA_ID_209706 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60374 RMVar_ID_60374 Human_SNP_ID_619231504 m1A Human chr17 - 18246772 18246772 18246772 GGAGGAGGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGAGGAAGCAACCG GGAGGAGGAAAAGAAGGAAGACAAGGAGGAGACGGCCGAGGGCAAAGAAGGCGAGGAAGCAACCG T G FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18246643..18247025 26863196 MeRIP-seq:(Medium) rs200455487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903438,Human_RBP_ID_26331375,Human_RBP_ID_27812365 Human_Splice_Rec_1787600,Human_Splice_Rec_1787700,Human_Splice_Rec_1787758,Human_Splice_Rec_1787816,Human_Splice_Rec_1787880,Human_Splice_Rec_1787888 Human_miRNA_ID_209706 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60375 RMVar_ID_60375 Human_SNP_ID_619231505 m1A Human chr17 - 18246775 18246773 18246776 CGAGGAGGAGGAAAAGAAGGAAGACAAGGAGGAGAAGGCCGAGGGCAAAGAAGGCGAGGAAGCAA CGAGGAGGAGGAAAAGAAGGAAGACAAGGAG___AAGGCCGAGGGCAAAGAAGGCGAGGAAGCAA TCTC T FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:18246738..18246893 26863196 MeRIP-seq:(Medium) rs139095003 Functional Loss DEL dbSNP153,HGVD 32..34 33 - - - Human_RBP_ID_903438,Human_RBP_ID_4409607,Human_RBP_ID_26331375,Human_RBP_ID_27812365 Human_Splice_Rec_1787600,Human_Splice_Rec_1787700,Human_Splice_Rec_1787758,Human_Splice_Rec_1787816,Human_Splice_Rec_1787880,Human_Splice_Rec_1787888 Human_miRNA_ID_209706 Clinvar_Rec_212 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_124511,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470,RMVar_hsa_circ_26514,RMVar_hsa_circ_182472 60376 RMVar_ID_60376 Human_SNP_ID_619231592 m1A Human chr17 - 18246949 18246949 18246949 GTTTGCGCGGCTGCCGGAAGAGGAGTTTGGCCACTTCTACACGCAGGACTGCTACGTCTTCCTCT GTTTGCGCGGCTGCCGGAAGAGGAGTTTGGCCGCTTCTACACGCAGGACTGCTACGTCTTCCTCT T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18246901..18246950 26863196 MeRIP-seq:(Medium) rs776501276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2496214,Human_RBP_ID_5466169,Human_RBP_ID_8824463 Human_Splice_Rec_1787599,Human_Splice_Rec_1787699,Human_Splice_Rec_1787757,Human_Splice_Rec_1787815,Human_Splice_Rec_1787879,Human_Splice_Rec_1787887 Human_miRNA_ID_878046 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 60377 RMVar_ID_60377 Human_SNP_ID_619231625 m1A Human chr17 - 18247023 18247023 18247023 CAGGCGGAGCAGCTGATGGAGGAGTGGAACGAAGACCTAGACGGCATGGAGGGTTTCGTGCTGGA CAGGCGGAGCAGCTGATGGAGGAGTGGAACGAGGACCTAGACGGCATGGAGGGTTTCGTGCTGGA T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18246893..18247073 26863196 MeRIP-seq:(Medium) rs1244215009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5582864,Human_RBP_ID_8825331,Human_RBP_ID_9289868,Human_RBP_ID_19078499,Human_RBP_ID_22442830 Human_Splice_Rec_1787598,Human_Splice_Rec_1787698,Human_Splice_Rec_1787756,Human_Splice_Rec_1787814,Human_Splice_Rec_1787886 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 60378 RMVar_ID_60378 Human_SNP_ID_619231811 m1A Human chr17 - 18247170 18247170 18247170 CCTGCCGCGGCAGCCGCCCATGTCGCTGGCCGAGGTGGGGGCAGGGCCGGGACCGGGGCGCGGGG CCTGCCGCGGCAGCCGCCCATGTCGCTGGCCGGGGTGGGGGCAGGGCCGGGACCGGGGCGCGGGG T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18247151..18247200 32194978 MeRIP-seq:(Medium) rs1182228845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821138,Human_RBP_ID_8824464,Human_RBP_ID_9288805 Human_Splice_Rec_1787597,Human_Splice_Rec_1787697,Human_Splice_Rec_1787755,Human_Splice_Rec_1787813,Human_Splice_Rec_1787885 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 60379 RMVar_ID_60379 Human_SNP_ID_619232096 m1A Human chr17 - 18247740 18247740 18247740 AGTCCCCGCGCCTGGTGCGCGCTGCCGCCCTCAAGCTGGGTCAGGAGCTGTGCGGGATGCTGCAC AGTCCCCGCGCCTGGTGCGCGCTGCCGCCCTCCAGCTGGGTCAGGAGCTGTGCGGGATGCTGCAC T G FLII Ensembl:ENSG00000177731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18247651..18247850 32194978 MeRIP-seq:(Medium) rs749538389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236878,Human_RBP_ID_4409627,Human_RBP_ID_8824467,Human_RBP_ID_9288806,Human_RBP_ID_18190738,Human_RBP_ID_26331376 Human_Splice_Rec_1787595,Human_Splice_Rec_1787695,Human_Splice_Rec_1787753,Human_Splice_Rec_1787811,Human_Splice_Rec_1787893 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 60380 RMVar_ID_60380 Human_SNP_ID_619232258 m1A Human chr17 - 18248035 18248035 18248035 ATCCCTTCCCTGCCATGCTCATCCTTCCTGCCAGGTGGGCCTGGGCTTGGGCTACCTGGAGCTGC ATCCCTTCCCTGCCATGCTCATCCTTCCTGCCTGGTGGGCCTGGGCTTGGGCTACCTGGAGCTGC T A FLII Ensembl:ENSG00000177731 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18247926..18248050 32194978 MeRIP-seq:(Medium) rs1419773791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4409638,Human_RBP_ID_5363847,Human_RBP_ID_8813941,Human_RBP_ID_19078500 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_182467,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 60381 RMVar_ID_60381 Human_SNP_ID_619232655 m1A Human chr17 - 18249133 18249133 18249133 GGAGCCTGTGCCCCTCAAGGGGACCTCTCTGGACCCAAGGTGAGCCCCAACAATGTGAGGTGGGG GGAGCCTGTGCCCCTCAAGGGGACCTCTCTGGGCCCAAGGTGAGCCCCAACAATGTGAGGTGGGG T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18249126..18249200 32194978 MeRIP-seq:(Medium) rs1238143262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821144,Human_RBP_ID_22444399,Human_RBP_ID_27449256 Human_Splice_Rec_1787586,Human_Splice_Rec_1787587,Human_Splice_Rec_1787656,Human_Splice_Rec_1787657,Human_Splice_Rec_1787686,Human_Splice_Rec_1787687,Human_Splice_Rec_1787744,Human_Splice_Rec_1787745,Human_Splice_Rec_1787802,Human_Splice_Rec_1787803,Human_Splice_Rec_1787898 RMVar_hsa_circ_120191,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_182467,RMVar_hsa_circ_92117,RMVar_hsa_circ_182470,RMVar_hsa_circ_36900,RMVar_hsa_circ_98653,RMVar_hsa_circ_44392,RMVar_hsa_circ_42434,RMVar_hsa_circ_182475 60382 RMVar_ID_60382 Human_SNP_ID_619233211 m1A Human chr17 + 18250866 18250866 18250866 GCACCTGCAGGAACTCCTCGCTCTCATCGCCCATCTCCTCCCGGACAGTGCGGCACTCAGCACCC GCACCTGCAGGAACTCCTCGCTCTCATCGCCCGTCTCCTCCCGGACAGTGCGGCACTCAGCACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18250842..18250966 26863196 MeRIP-seq:(Medium) rs1347557885 Functional Loss SNV dbSNP153 33..33 33 - - - 60383 RMVar_ID_60383 Human_SNP_ID_619233405 m1A Human chr17 + 18251326 18251326 18251326 AGAACTTGCCGTGGAAGGCTTCCTCCACCAGCACAGGCACGAAGTTCTCTATCTGCCAGATGGTC AGAACTTGCCGTGGAAGGCTTCCTCCACCAGCGCAGGCACGAAGTTCTCTATCTGCCAGATGGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18251276..18251500 32194978 MeRIP-seq:(Medium) rs1268474939 Functional Loss SNV dbSNP153 33..33 33 - - - 60384 RMVar_ID_60384 Human_SNP_ID_619233464 m1A Human chr17 - 18251453 18251453 18251453 GCCCCCAGGAGAGCGCAGATGCCCGGGCCCCCAGCGGGAAGGTGCGGCGTTGGGACCAGGGCCTG GCCCCCAGGAGAGCGCAGATGCCCGGGCCCCCGGCGGGAAGGTGCGGCGTTGGGACCAGGGCCTG T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18251368..18251488 26863196 MeRIP-seq:(Medium) rs1181735156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236882,Human_RBP_ID_903443,Human_RBP_ID_3951916,Human_RBP_ID_5525409,Human_RBP_ID_8825337,Human_RBP_ID_9375477 Human_Splice_Rec_1787580,Human_Splice_Rec_1787650,Human_Splice_Rec_1787680,Human_Splice_Rec_1787738,Human_Splice_Rec_1787796,Human_Splice_Rec_1787906 Human_miRNA_ID_2685693 RMVar_hsa_circ_120191,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_182467,RMVar_hsa_circ_98780,RMVar_hsa_circ_92117,RMVar_hsa_circ_182470,RMVar_hsa_circ_98653,RMVar_hsa_circ_182475,RMVar_hsa_circ_121111,RMVar_hsa_circ_182476,RMVar_hsa_circ_182477 60385 RMVar_ID_60385 Human_SNP_ID_619233538 m1A Human chr17 + 18251663 18251663 18251663 CAGCAGAAGCTAAGGCTCCCTGCCTTGTCCCAACCCTGGCCTGGCTCACCTCCTGCTTTTTGTTC CAGCAGAAGCTAAGGCTCCCTGCCTTGTCCCACCCCTGGCCTGGCTCACCTCCTGCTTTTTGTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18251660..18251801 26863196 MeRIP-seq:(Medium) rs775299530 Functional Loss SNV dbSNP153 33..33 33 - - - 60386 RMVar_ID_60386 Human_SNP_ID_619234577 m1A Human chr17 - 18254645 18254645 18254645 ACACCATCCCCAACCAGCTCTTCATCAACCTCACTGACCTACTATACCTGGACCTCAGCGAGAAC ACACCATCCCCAACCAGCTCTTCATCAACCTCGCTGACCTACTATACCTGGACCTCAGCGAGAAC T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18254498..18254798 26863196 MeRIP-seq:(Medium) rs146773001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3514222,Human_RBP_ID_18530488,Human_RBP_ID_27449259 Human_Splice_Rec_1787566,Human_Splice_Rec_1787636,Human_Splice_Rec_1787724,Human_Splice_Rec_1787782,Human_Splice_Rec_1787946,Human_Splice_Rec_1787966,Human_Splice_Rec_1787978 Human_miRNA_ID_189653,Human_miRNA_ID_2007566 RMVar_hsa_circ_98780,RMVar_hsa_circ_92117,RMVar_hsa_circ_182470,RMVar_hsa_circ_98653,RMVar_hsa_circ_182475,RMVar_hsa_circ_93102,RMVar_hsa_circ_182477,RMVar_hsa_circ_182479,RMVar_hsa_circ_20347,RMVar_hsa_circ_113612,RMVar_hsa_circ_182483,RMVar_hsa_circ_369722,RMVar_hsa_circ_182481 60387 RMVar_ID_60387 Human_SNP_ID_619235166 m1A Human chr17 - 18256658 18256658 18256658 GGCCTTCCTGGATGGTGCAGAGTTGTGGAGGCAGGCAGGGACTCTGGACACCCCACCCACCCTGC GGCCTTCCTGGATGGTGCAGAGTTGTGGAGGCGGGCAGGGACTCTGGACACCCCACCCACCCTGC T C FLII Ensembl:ENSG00000177731 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18256656..18256889 26863196 MeRIP-seq:(Medium) rs980363409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899537,Human_RBP_ID_5362587,Human_RBP_ID_23257134 RMVar_hsa_circ_93102,RMVar_hsa_circ_182479,RMVar_hsa_circ_182484,RMVar_hsa_circ_96044 60388 RMVar_ID_60388 Human_SNP_ID_619235247 m1A Human chr17 + 18256940 18256940 18256940 CCAGCTTCTGCAGGGCGGCCAGCTCCTCGGGCAGGTAGCAGAGGCCAGTGCGGTTCAGCTTCAGC CCAGCTTCTGCAGGGCGGCCAGCTCCTCGGGCTGGTAGCAGAGGCCAGTGCGGTTCAGCTTCAGC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:18256926..18257063 26863196 MeRIP-seq:(Medium) rs1229031001 Functional Loss SNV dbSNP153 33..33 33 - - - 60389 RMVar_ID_60389 Human_SNP_ID_619235709 m1A Human chr17 + 18258586 18258586 18258586 GAAGCGGAGGCCAAGCGGGCCGGGCGGAAGAGAAGGCCTGCAGGGAGGCCCGGCACGCGCCCGGC GAAGCGGAGGCCAAGCGGGCCGGGCGGAAGAGGAGGCCTGCAGGGAGGCCCGGCACGCGCCCGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18258584..18258725 26863196 MeRIP-seq:(Medium) rs1240397573 Functional Loss SNV dbSNP153 33..33 33 - - - 60390 RMVar_ID_60390 Human_SNP_ID_619235710 m1A Human chr17 + 18258586 18258586 18258586 GAAGCGGAGGCCAAGCGGGCCGGGCGGAAGAGAAGGCCTGCAGGGAGGCCCGGCACGCGCCCGGC GAAGCGGAGGCCAAGCGGGCCGGGCGGAAGAGTAGGCCTGCAGGGAGGCCCGGCACGCGCCCGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:18258584..18258725 26863196 MeRIP-seq:(Medium) rs1240397573 Functional Loss SNV dbSNP153 33..33 33 - - - 60391 RMVar_ID_60391 Human_SNP_ID_619236951 m1A Human chr17 + 18262757 18262757 18262757 CAGAGTTCTCCCAGAAACGGGGGAAGCGGCGTAGCGACGAAGGGCTGGGCAGCATGGTGGACTTC CAGAGTTCTCCCAGAAACGGGGGAAGCGGCGTCGCGACGAAGGGCTGGGCAGCATGGTGGACTTC A C MIEF2 Ensembl:ENSG00000177427 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18260731..18262756 32194978 MeRIP-seq:(Medium) rs1264354231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1787990,Human_Splice_Rec_1787996,Human_Splice_Rec_1788002,Human_Splice_Rec_1788010,Human_Splice_Rec_1788016,Human_Splice_Rec_1788022,Human_Splice_Rec_1788024,Human_Splice_Rec_1788030 60392 RMVar_ID_60392 Human_SNP_ID_619237064 m1A Human chr17 + 18263104 18263104 18263104 GACTGTGCTTGCAGTTCATTGACAGGGCCACTAGCCCGCGGGATGAGGATGACACCAAGGCAGAC GACTGTGCTTGCAGTTCATTGACAGGGCCACTCGCCCGCGGGATGAGGATGACACCAAGGCAGAC A C MIEF2 Ensembl:ENSG00000177427 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18263102..18263252 32194978 MeRIP-seq:(Medium) rs759080457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1787992,Human_Splice_Rec_1787998,Human_Splice_Rec_1788004,Human_Splice_Rec_1788012,Human_Splice_Rec_1788018,Human_Splice_Rec_1788026,Human_Splice_Rec_1788032 RMVar_hsa_circ_182485 60393 RMVar_ID_60393 Human_SNP_ID_619237426 m1A Human chr17 - 18263998 18263998 18263998 GCACCAGGCTCCACAGGCCCGGCTCCAGCACCAGTGGCACCAGGAGACGCACATGGTCCGCAGCC GCACCAGGCTCCACAGGCCCGGCTCCAGCACCGGTGGCACCAGGAGACGCACATGGTCCGCAGCC T C lnc-TOP3A-1 RNACentral:URS0000D59144 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18263873..18264717 32194978 MeRIP-seq:(Medium) rs1205413878 Functional Loss SNV dbSNP153 33..33 33 - - - 60394 RMVar_ID_60394 Human_SNP_ID_619239572 m1A Human chr17 - 18271837 18271837 18271837 GCTGGTCTCAAACTCGTGACCTCAGGTGATCTACCAGCCTCGGCCTCCCAAAGTGCTAGGATTAA GCTGGTCTCAAACTCGTGACCTCAGGTGATCTGCCAGCCTCGGCCTCCCAAAGTGCTAGGATTAA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1193575347 Functional Loss SNV dbSNP153 33..33 33 - - - 60395 RMVar_ID_60395 Human_SNP_ID_619254938 m1A Human chr17 + 18324444 18324444 18324444 AGTTTCTTGCAGCCTTGAAAATTTTATTCCCTAAGTGGGGACAGCTCTGGTATTACTGCTTCTTT AGTTTCTTGCAGCCTTGAAAATTTTATTCCCTGAGTGGGGACAGCTCTGGTATTACTGCTTCTTT A G SMCR8 Ensembl:ENSG00000176994 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs56001517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3514293,Human_RBP_ID_6566533,Human_RBP_ID_26458763 60396 RMVar_ID_60396 Human_SNP_ID_619255937 m1A Human chr17 + 18328779 18328778 18328780 CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGAAGAGAGAGGCGAAGCTCTCAACCTCCTCCCGGA CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGA__AGAGAGGCGAAGCTCTCAACCTCCTCCCGGA AAG A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18328651..18328900 32194978 MeRIP-seq:(Medium) rs992639703 Functional Loss DEL dbSNP153 33..34 33 - - - 60397 RMVar_ID_60397 Human_SNP_ID_619255938 m1A Human chr17 + 18328779 18328779 18328779 CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGAAGAGAGAGGCGAAGCTCTCAACCTCCTCCCGGA CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGACGAGAGAGGCGAAGCTCTCAACCTCCTCCCGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18328651..18328900 32194978 MeRIP-seq:(Medium) rs1323562284 Functional Loss SNV dbSNP153 33..33 33 - - - 60398 RMVar_ID_60398 Human_SNP_ID_619259447 m1A Human chr17 + 18340727 18340727 18340727 ACTGGTGAACAAGGTGACTTTCCGCCCCGCGCATCACCTGCGATGATCAGCTTCGGGTGGAAGAG ACTGGTGAACAAGGTGACTTTCCGCCCCGCGCCTCACCTGCGATGATCAGCTTCGGGTGGAAGAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18340717..18340868 32194978 MeRIP-seq:(Medium) rs1262559632 Functional Loss SNV dbSNP153 33..33 33 - - - 60399 RMVar_ID_60399 Human_SNP_ID_619263872 m1A Human chr17 + 18355994 18355982 18355995 CCGTTGACTGGCATCGTCATTGCACTGGTTCGAAGCTGCCTAAAAAAATGGGAAAAACATGTGTA CCGTTGACTGGCATCGTCATT_____________GCTGCCTAAAAAAATGGGAAAAACATGTGTA TGCACTGGTTCGAA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18355891..18363039 26863196 MeRIP-seq:(Medium) rs1021952457 Functional Loss DEL dbSNP153 22..34 33 - - - 60400 RMVar_ID_60400 Human_SNP_ID_619266153 m1A Human chr17 - 18363425 18363425 18363425 CTGGCCCGCGGCGGTGCGCGGGGCGTTGGGTCAGCGGGTCTGGGACTGGTGGCACCGGCGGCGGC CTGGCCCGCGGCGGTGCGCGGGGCGTTGGGTCTGCGGGTCTGGGACTGGTGGCACCGGCGGCGGC T A SHMT1 Ensembl:ENSG00000176974 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:18363300..18363473 26863196 MeRIP-seq:(Medium) rs1471852251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238181,Human_RBP_ID_4410070,Human_RBP_ID_5419873,Human_RBP_ID_18419552,Human_RBP_ID_22442833,Human_RBP_ID_22959778 Human_Splice_Rec_1788329,Human_Splice_Rec_1788361,Human_Splice_Rec_1788383,Human_Splice_Rec_1788403,Human_Splice_Rec_1788423,Human_Splice_Rec_1788443,Human_Splice_Rec_1788447 60401 RMVar_ID_60401 Human_SNP_ID_619266173 m1A Human chr17 + 18363465 18363465 18363465 CGCCCCGCGCACCGCCGCGGGCCAGCCACGTGACCAGCCGCTCCAACCCCAAACCCCGAACTTGG CGCCCCGCGCACCGCCGCGGGCCAGCCACGTGCCCAGCCGCTCCAACCCCAAACCCCGAACTTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:18363263..18363525;chr17:18363188..18363525;chr17:18363288..18363525 26863196 MeRIP-seq:(Medium) rs1002200622 Functional Loss SNV dbSNP153 33..33 33 - - - 60402 RMVar_ID_60402 Human_SNP_ID_619272137 m1A Human chr17 - 18383365 18383365 18383365 CGCCCTGCCCCCAGCGCACCTGGATGGGCCCCACCGCGGGGTGCCGCAGCTCCACCATGCGCTTG CGCCCTGCCCCCAGCGCACCTGGATGGGCCCCGCCGCGGGGTGCCGCAGCTCCACCATGCGCTTG T C AL353997.2 Ensembl:ENSG00000264177 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18383317..18383578 26863196 MeRIP-seq:(Medium) rs1297771258 Functional Loss SNV dbSNP153 33..33 33 - - - 60403 RMVar_ID_60403 Human_SNP_ID_619272644 m1A Human chr17 + 18384946 18384946 18384946 ATGGGTAGAAAGAGATGGGGGAGAGACAGAGGAGGCTGAGAGGGAGAGGAGGATGGAGAGAGCAG ATGGGTAGAAAGAGATGGGGGAGAGACAGAGGCGGCTGAGAGGGAGAGGAGGATGGAGAGAGCAG A C EVPLL Ensembl:ENSG00000214860 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18384941..18385033 26863196 MeRIP-seq:(Medium) rs1412734160 Functional Loss SNV dbSNP153 33..33 33 - - - 60404 RMVar_ID_60404 Human_SNP_ID_619272657 m1A Human chr17 + 18384988 18384988 18384988 GGAGAGGAGGATGGAGAGAGCAGAGAGAGAGAAACAGAGATGGGGAAAGGGGCAAGAGATGACAA GGAGAGGAGGATGGAGAGAGCAGAGAGAGAGAGACAGAGATGGGGAAAGGGGCAAGAGATGACAA A G EVPLL Ensembl:ENSG00000214860 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18384939..18385053 26863196 MeRIP-seq:(Medium) rs1052827132 Functional Loss SNV dbSNP153 33..33 33 - - - 60405 RMVar_ID_60405 Human_SNP_ID_619278943 m1A Human chr17 - 18410921 18410920 18410922 AGGCAGGGAACGAGGTGGGGAGGGGAAGAGAAAGGCAGAAAGACGGGCTGAGAAGAGTGCTGGGA AGGCAGGGAACGAGGTGGGGAGGGGAAGAGA__GGCAGAAAGACGGGCTGAGAAGAGTGCTGGGA CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18410769..18411168 26863196 MeRIP-seq:(Medium) rs1324248301 Functional Loss DEL dbSNP153 32..33 33 - - - 60406 RMVar_ID_60406 Human_SNP_ID_619279106 m1A Human chr17 - 18411290 18411290 18411290 ACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGGAA ACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAGAAAAAACTGCGGGGGAGAAGAAGGTGCGGGAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18411228..18411348 26863196 MeRIP-seq:(Medium) rs1371784733 Functional Loss SNV dbSNP153 33..33 33 - - - 60407 RMVar_ID_60407 Human_SNP_ID_619279107 m1A Human chr17 - 18411292 18411292 18411292 AGACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGG AGACTGAGGGGAAGAAAACGGTGGGGAAGGGGGAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18411229..18411348 26863196 MeRIP-seq:(Medium) rs539851579 Functional Loss SNV dbSNP153 33..33 33 - - - 60408 RMVar_ID_60408 Human_SNP_ID_619279374 m1A Human chr17 + 18411696 18411692 18411696 CTTCTCCATTTTCTTGCCGCCTCCATATCCCCACCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG CTTCTCCATTTTCTTGCCGCCTCCATATC____CCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG CCCCA C LINC02076 Ensembl:ENSG00000220161 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18411453..18411874 26863196 MeRIP-seq:(Medium) rs1392122296 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5290882 60409 RMVar_ID_60409 Human_SNP_ID_619279375 m1A Human chr17 + 18411696 18411694 18411696 CTTCTCCATTTTCTTGCCGCCTCCATATCCCCACCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG CTTCTCCATTTTCTTGCCGCCTCCATATCCC__CCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG CCA C LINC02076 Ensembl:ENSG00000220161 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18411453..18411874 26863196 MeRIP-seq:(Medium) rs759208950 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5290882 60410 RMVar_ID_60410 Human_SNP_ID_619279376 m1A Human chr17 + 18411696 18411696 18411696 CTTCTCCATTTTCTTGCCGCCTCCATATCCCCACCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG CTTCTCCATTTTCTTGCCGCCTCCATATCCCCGCCTTCTTCTCGCAGCAGCGTCTTCCTGCCGCG A G LINC02076 Ensembl:ENSG00000220161 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18411453..18411874 26863196 MeRIP-seq:(Medium) rs1455384669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5290882 60411 RMVar_ID_60411 Human_SNP_ID_619279380 m1A Human chr17 - 18411700 18411700 18411700 AAAGCGCGGCAGGAAGACGCTGCTGCGAGAAGAAGGTGGGGATATGGAGGCGGCAAGAAAATGGA AAAGCGCGGCAGGAAGACGCTGCTGCGAGAAGGAGGTGGGGATATGGAGGCGGCAAGAAAATGGA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:18411601..18411700 26863410 MeRIP-seq:(Medium) rs755304745 Functional Loss SNV dbSNP153 33..33 33 - - - 60412 RMVar_ID_60412 Human_SNP_ID_619279489 m1A Human chr17 - 18411803 18411803 18411803 GAGAAAACGGTTGTGGGGAAGGCGCGGGGAGAAGACAGTGAGGAGAAGAGGGCGTGGGGAGAGGA GAGAAAACGGTTGTGGGGAAGGCGCGGGGAGAGGACAGTGAGGAGAAGAGGGCGTGGGGAGAGGA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:18411581..18411850 26863196 MeRIP-seq:(Medium) rs1305161756 Functional Loss SNV dbSNP153 33..33 33 - - - 60413 RMVar_ID_60413 Human_SNP_ID_619361952 m1A Human chr17 - 18781322 18781322 18781322 AGCCAGTCCCAGGAGCCGCCACCCTCCCAGCGAGCCCTCAGCCCCTCACCTGCTGCAACATGGCG AGCCAGTCCCAGGAGCCGCCACCCTCCCAGCGCGCCCTCAGCCCCTCACCTGCTGCAACATGGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18781284..18781530 26863196 MeRIP-seq:(Medium) rs74697973 Functional Loss SNV dbSNP153 33..33 33 - - - 60414 RMVar_ID_60414 Human_SNP_ID_619361956 m1A Human chr17 + 18781330 18781330 18781330 TGCAGCAGGTGAGGGGCTGAGGGCTCGCTGGGAGGGTGGCGGCTCCTGGGACTGGCTCTGCAGGT TGCAGCAGGTGAGGGGCTGAGGGCTCGCTGGGGGGGTGGCGGCTCCTGGGACTGGCTCTGCAGGT A G TVP23B Ensembl:ENSG00000171928 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18781204..18781378 26863196 MeRIP-seq:(Medium) rs757531147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21974219 60415 RMVar_ID_60415 Human_SNP_ID_619361961 m1A Human chr17 - 18781334 18781334 18781334 CGGAACCTGCAGAGCCAGTCCCAGGAGCCGCCACCCTCCCAGCGAGCCCTCAGCCCCTCACCTGC CGGAACCTGCAGAGCCAGTCCCAGGAGCCGCCGCCCTCCCAGCGAGCCCTCAGCCCCTCACCTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18781221..18781399 26863196 MeRIP-seq:(Medium) rs746035332 Functional Loss SNV dbSNP153 33..33 33 - - - 60416 RMVar_ID_60416 Human_SNP_ID_619362022 m1A Human chr17 - 18781486 18781486 18781486 TTGCTCTGCGCCGCACGGGTCACGCCGCCCCCAGCGGCCTCAGAACCCCCAGCAGCCCTCCTCAG TTGCTCTGCGCCGCACGGGTCACGCCGCCCCCTGCGGCCTCAGAACCCCCAGCAGCCCTCCTCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18781448..18781533 26863196 MeRIP-seq:(Medium) rs1021644213 Functional Loss SNV dbSNP153 33..33 33 - - - 60417 RMVar_ID_60417 Human_SNP_ID_619362023 m1A Human chr17 - 18781486 18781486 18781486 TTGCTCTGCGCCGCACGGGTCACGCCGCCCCCAGCGGCCTCAGAACCCCCAGCAGCCCTCCTCAG TTGCTCTGCGCCGCACGGGTCACGCCGCCCCCGGCGGCCTCAGAACCCCCAGCAGCCCTCCTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18781448..18781533 26863196 MeRIP-seq:(Medium) rs1021644213 Functional Loss SNV dbSNP153 33..33 33 - - - 60418 RMVar_ID_60418 Human_SNP_ID_619377922 m1A Human chr17 + 18855933 18855929 18855934 GGCGGGTGAGAAAGGGCAATGGAGAAGGAAGGAGAGGAGACCGTGCAGACACTGCAAGTGCCAGA GGCGGGTGAGAAAGGGCAATGGAGAAGGA_____AGGAGACCGTGCAGACACTGCAAGTGCCAGA AAGGAG A PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18855900..18855984 26863196 MeRIP-seq:(Medium) rs1421646497 Functional Loss DEL dbSNP153 30..34 33 - - - 60419 RMVar_ID_60419 Human_SNP_ID_619378055 m1A Human chr17 + 18856406 18856406 18856406 CAGCGCAGAAGGGACGTGAGCCCAGCCGAGGTACCGCTGAAGAGGAATCAATTTTGGTATGCAGA CAGCGCAGAAGGGACGTGAGCCCAGCCGAGGTGCCGCTGAAGAGGAATCAATTTTGGTATGCAGA A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:18856355..18856453;chr17:18856357..18856463 26863196 MeRIP-seq:(Medium) rs371246409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23714605 Human_Splice_Rec_1789553,Human_Splice_Rec_1789561,Human_Splice_Rec_1789577,Human_Splice_Rec_1789611,Human_Splice_Rec_1789623,Human_Splice_Rec_1789637,Human_Splice_Rec_1789657,Human_Splice_Rec_1789675,Human_Splice_Rec_1789685 60420 RMVar_ID_60420 Human_SNP_ID_619378056 m1A Human chr17 + 18856406 18856406 18856406 CAGCGCAGAAGGGACGTGAGCCCAGCCGAGGTACCGCTGAAGAGGAATCAATTTTGGTATGCAGA CAGCGCAGAAGGGACGTGAGCCCAGCCGAGGTTCCGCTGAAGAGGAATCAATTTTGGTATGCAGA A T PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:18856355..18856453;chr17:18856357..18856463 26863196 MeRIP-seq:(Medium) rs371246409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23714605 Human_Splice_Rec_1789553,Human_Splice_Rec_1789561,Human_Splice_Rec_1789577,Human_Splice_Rec_1789611,Human_Splice_Rec_1789623,Human_Splice_Rec_1789637,Human_Splice_Rec_1789657,Human_Splice_Rec_1789675,Human_Splice_Rec_1789685 60421 RMVar_ID_60421 Human_SNP_ID_619378555 m1A Human chr17 - 18858252 18858252 18858252 GCCACTGGCTCCCGCCCGCCTACCTGGCCCCGACCCCAGCCCCGGCCCCGCCGCAGCCTCAGCTG GCCACTGGCTCCCGCCCGCCTACCTGGCCCCGCCCCCAGCCCCGGCCCCGCCGCAGCCTCAGCTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18858170..18858450 32194978 MeRIP-seq:(Medium) rs934823398 Functional Loss SNV dbSNP153 33..33 33 - - - 60422 RMVar_ID_60422 Human_SNP_ID_619382210 m1A Human chr17 - 18872599 18872599 18872599 ATGAAAACATCTTTTCCCCTCACAGACTCTTGAATTTGTACTCTTGTTTCTGGCAGGAAAAGGAA ATGAAAACATCTTTTCCCCTCACAGACTCTTGGATTTGTACTCTTGTTTCTGGCAGGAAAAGGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18865803..18877853 32194978 MeRIP-seq:(Medium) rs561935017 Functional Loss SNV dbSNP153 33..33 33 - - - 60423 RMVar_ID_60423 Human_SNP_ID_619406584 m1A Human chr17 + 18969380 18969380 18969380 TGGCTGCTGTAATCTACACGGACGCCCTGCAGACGCTCATCATGGTGGTGGGGGCTGTCATCCTG TGGCTGCTGTAATCTACACGGACGCCCTGCAGCCGCTCATCATGGTGGTGGGGGCTGTCATCCTG A C SLC5A10 Ensembl:ENSG00000154025 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:18969331..18969451 26863196 MeRIP-seq:(Medium) rs760144236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1789948,Human_Splice_Rec_1789949,Human_Splice_Rec_1789976,Human_Splice_Rec_1789977,Human_Splice_Rec_1790028,Human_Splice_Rec_1790029 60424 RMVar_ID_60424 Human_SNP_ID_619406745 m1A Human chr17 + 18970001 18970001 18970001 GCAGAGCCAGGAGGATCCCTCAGAGAGTGAACAAATCTCTAAAGACTCTTCCAGACTCAGACACT GCAGAGCCAGGAGGATCCCTCAGAGAGTGAACGAATCTCTAAAGACTCTTCCAGACTCAGACACT A G SLC5A10 Ensembl:ENSG00000154025 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18969951..18970000 32194978 MeRIP-seq:(Medium) rs1361146440 Functional Loss SNV dbSNP153 33..33 33 - - - 60425 RMVar_ID_60425 Human_SNP_ID_619415493 m1A Human chr17 - 19004096 19004096 19004096 CGAGCGCGCGGTGCCCCAGCTGGGCCGGAGCTAGGAGCTGGACCTTGCCCACCCACCCCCGGCAG CGAGCGCGCGGTGCCCCAGCTGGGCCGGAGCTGGGAGCTGGACCTTGCCCACCCACCCCCGGCAG T C FAM83G Ensembl:ENSG00000188522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19004046..19004138 26863196 MeRIP-seq:(Medium) rs557284855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466160 Human_Splice_Rec_1790050 60426 RMVar_ID_60426 Human_SNP_ID_619415511 m1A Human chr17 + 19004161 19004161 19004161 GGGGCCTCTCCGCGGCCTCTGCTTCTCTGCCCATGAGCAATCTGCGGGAAAGACCTGATGAGCCC GGGGCCTCTCCGCGGCCTCTGCTTCTCTGCCCGTGAGCAATCTGCGGGAAAGACCTGATGAGCCC A G SLC5A10 Ensembl:ENSG00000154025 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:19004152..19004754 26863410 MeRIP-seq:(Medium) rs1408236671 Functional Loss SNV dbSNP153 33..33 33 - - - 60427 RMVar_ID_60427 Human_SNP_ID_619415669 m1A Human chr17 + 19004736 19004736 19004736 CTTACCGAGCGGGCGCTGGCGGAGCGGGGCGCACACGCGGCGGCTGCGGCGGCGGCGCGAGGCTG CTTACCGAGCGGGCGCTGGCGGAGCGGGGCGCCCACGCGGCGGCTGCGGCGGCGGCGCGAGGCTG A C SLC5A10 Ensembl:ENSG00000154025 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:19004685..19004806 26863410 MeRIP-seq:(Medium) rs954338721 Functional Loss SNV dbSNP153 33..33 33 - - - 60428 RMVar_ID_60428 Human_SNP_ID_619415672 m1A Human chr17 - 19004748 19004739 19004748 CGCGCCCCCGCCCAGCCTCGCGCCGCCGCCGCAGCCGCCGCGTGTGCGCCCCGCTCCGCCAGCGC CGCGCCCCCGCCCAGCCTCGCGCCGCCGCCGC_________GTGTGCGCCCCGCTCCGCCAGCGC CGCGGCGGCT C FAM83G Ensembl:ENSG00000188522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19004682..19004780 26863196 MeRIP-seq:(Medium) rs539060717 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4410322 Human_Splice_Rec_1790049 60429 RMVar_ID_60429 Human_SNP_ID_619438060 m1A Human chr17 + 19188093 19188093 19188093 AGTTTCTCTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG AGTTTCTCTGAACGTGTAGAGCACCGAAAACCCCGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG A C SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19188062..19188150 26863196 MeRIP-seq:(Medium) rs1451686516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2496433,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883499,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60430 RMVar_ID_60430 Human_SNP_ID_619438061 m1A Human chr17 + 19188093 19188093 19188093 AGTTTCTCTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG AGTTTCTCTGAACGTGTAGAGCACCGAAAACCGCGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG A G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19188062..19188150 26863196 MeRIP-seq:(Medium) rs1451686516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2496433,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883499,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60431 RMVar_ID_60431 Human_SNP_ID_619438062 m1A Human chr17 + 19188093 19188093 19188093 AGTTTCTCTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG AGTTTCTCTGAACGTGTAGAGCACCGAAAACCTCGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCG A T SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19188062..19188150 26863196 MeRIP-seq:(Medium) rs1451686516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2496433,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883499,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60432 RMVar_ID_60432 Human_SNP_ID_619438071 m1A Human chr17 + 19188096 19188096 19188096 TTCTCTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGA TTCTCTGAACGTGTAGAGCACCGAAAACCACGCGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGA A C SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:19188029..19188178 26863196 MeRIP-seq:(Medium) rs780214079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2496433,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60433 RMVar_ID_60433 Human_SNP_ID_619438072 m1A Human chr17 + 19188096 19188096 19188096 TTCTCTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGA TTCTCTGAACGTGTAGAGCACCGAAAACCACGGGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGA A G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:19188029..19188178 26863196 MeRIP-seq:(Medium) rs780214079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2496433,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60434 RMVar_ID_60434 Human_SNP_ID_619438073 m1A Human chr17 + 19188100 19188097 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAG___GAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC GGAA G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs760680076 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60435 RMVar_ID_60435 Human_SNP_ID_619438078 m1A Human chr17 + 19188100 19188098 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAGG__GAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC GAA G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs1567835076 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60436 RMVar_ID_60436 Human_SNP_ID_619438088 m1A Human chr17 + 19188100 19188100 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAGGACGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC A C SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs531318002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60437 RMVar_ID_60437 Human_SNP_ID_619438089 m1A Human chr17 + 19188100 19188100 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAGGAGGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC A G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs531318002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60438 RMVar_ID_60438 Human_SNP_ID_619438090 m1A Human chr17 + 19188100 19188100 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAGGATGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC A T SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs531318002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 60439 RMVar_ID_60439 Human_SNP_ID_619438183 m1A Human chr17 - 19188126 19188124 19188126 TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCACGCTCAGGAGAAAACGCTACCTCTCTTCCTCG TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTC__GCTCAGGAGAAAACGCTACCTCTCTTCCTCG CGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:19187980..19188210;chr17:19187998..19188129 26863196 MeRIP-seq:(Medium) rs1491534409 Functional Loss DEL dbSNP153 33..34 33 - - - 60440 RMVar_ID_60440 Human_SNP_ID_619438191 m1A Human chr17 - 19188126 19188126 19188126 TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCACGCTCAGGAGAAAACGCTACCTCTCTTCCTCG TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCTCGCTCAGGAGAAAACGCTACCTCTCTTCCTCG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:19187980..19188210;chr17:19187998..19188129 26863196 MeRIP-seq:(Medium) rs778528157 Functional Loss SNV dbSNP153 33..33 33 - - - 60441 RMVar_ID_60441 Human_SNP_ID_619438192 m1A Human chr17 - 19188126 19188126 19188126 TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCACGCTCAGGAGAAAACGCTACCTCTCTTCCTCG TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCGCGCTCAGGAGAAAACGCTACCTCTCTTCCTCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:19187980..19188210;chr17:19187998..19188129 26863196 MeRIP-seq:(Medium) rs778528157 Functional Loss SNV dbSNP153 33..33 33 - - - 60442 RMVar_ID_60442 Human_SNP_ID_619438193 m1A Human chr17 - 19188126 19188126 19188126 TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCACGCTCAGGAGAAAACGCTACCTCTCTTCCTCG TTGCAGCCAAGCAACGCCAGAAAGCCGGCTTCCCGCTCAGGAGAAAACGCTACCTCTCTTCCTCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:19187980..19188210;chr17:19187998..19188129 26863196 MeRIP-seq:(Medium) rs778528157 Functional Loss SNV dbSNP153 33..33 33 - - - 60443 RMVar_ID_60443 Human_SNP_ID_619438199 m1A Human chr17 + 19188128 19188128 19188128 AGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCCGGCTTTCTGGCGTTGCTTGGCTGCAACT AGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGCAGCCGGCTTTCTGGCGTTGCTTGGCTGCAACT A C SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs537999577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_1547070,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5649293,Human_RBP_ID_8253215,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_9290531,Human_RBP_ID_10483700,Human_RBP_ID_12917158,Human_RBP_ID_17190190,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17693558,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18513487,Human_RBP_ID_18530492,Human_RBP_ID_18691022,Human_RBP_ID_18926827,Human_RBP_ID_21960120,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22524083,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22960098,Human_RBP_ID_23110430,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24545264,Human_RBP_ID_24559538,Human_RBP_ID_26575766,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_27449494,Human_RBP_ID_27796892 60444 RMVar_ID_60444 Human_SNP_ID_619438200 m1A Human chr17 + 19188128 19188128 19188128 AGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCCGGCTTTCTGGCGTTGCTTGGCTGCAACT AGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGGAGCCGGCTTTCTGGCGTTGCTTGGCTGCAACT A G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs537999577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_1547070,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5649293,Human_RBP_ID_8253215,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_9290531,Human_RBP_ID_10483700,Human_RBP_ID_12917158,Human_RBP_ID_17190190,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17693558,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18513487,Human_RBP_ID_18530492,Human_RBP_ID_18691022,Human_RBP_ID_18926827,Human_RBP_ID_21960120,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22524083,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22960098,Human_RBP_ID_23110430,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24545264,Human_RBP_ID_24559538,Human_RBP_ID_26575766,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_27449494,Human_RBP_ID_27796892 60445 RMVar_ID_60445 Human_SNP_ID_619441237 m1A Human chr17 + 19237528 19237528 19237528 GCAGCGGCGCACCCACGCCGGCCCGGAGGAGCAGAGGTGAGCCACAGCCCGTGGGGCTCCAAGGC GCAGCGGCGCACCCACGCCGGCCCGGAGGAGCCGAGGTGAGCCACAGCCCGTGGGGCTCCAAGGC A C EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr17:19237477..19237640;chr17:19237526..19237550 26863196,32194978 MeRIP-seq:(Medium) rs1258283778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419906,Human_RBP_ID_19081754 Human_Splice_Rec_1790205,Human_Splice_Rec_1790225,Human_Splice_Rec_1790243,Human_Splice_Rec_1790245,Human_Splice_Rec_1790251,Human_Splice_Rec_1790253,Human_Splice_Rec_1790261,Human_Splice_Rec_1790275,Human_Splice_Rec_1790289,Human_Splice_Rec_1790295,Human_Splice_Rec_1790307,Human_Splice_Rec_1790321,Human_Splice_Rec_1790327,Human_Splice_Rec_1790335 RMVar_hsa_circ_182564,RMVar_hsa_circ_110734,RMVar_hsa_circ_119994,RMVar_hsa_circ_182565 60446 RMVar_ID_60446 Human_SNP_ID_619441238 m1A Human chr17 + 19237528 19237528 19237528 GCAGCGGCGCACCCACGCCGGCCCGGAGGAGCAGAGGTGAGCCACAGCCCGTGGGGCTCCAAGGC GCAGCGGCGCACCCACGCCGGCCCGGAGGAGCGGAGGTGAGCCACAGCCCGTGGGGCTCCAAGGC A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr17:19237477..19237640;chr17:19237526..19237550 26863196,32194978 MeRIP-seq:(Medium) rs1258283778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419906,Human_RBP_ID_19081754 Human_Splice_Rec_1790205,Human_Splice_Rec_1790225,Human_Splice_Rec_1790243,Human_Splice_Rec_1790245,Human_Splice_Rec_1790251,Human_Splice_Rec_1790253,Human_Splice_Rec_1790261,Human_Splice_Rec_1790275,Human_Splice_Rec_1790289,Human_Splice_Rec_1790295,Human_Splice_Rec_1790307,Human_Splice_Rec_1790321,Human_Splice_Rec_1790327,Human_Splice_Rec_1790335 RMVar_hsa_circ_182564,RMVar_hsa_circ_110734,RMVar_hsa_circ_119994,RMVar_hsa_circ_182565 60447 RMVar_ID_60447 Human_SNP_ID_619441320 m1A Human chr17 + 19237688 19237688 19237688 TGCGCCCCTGCCGCCCCGCTGGTCCCTACGCCAGGCTCTGGGGGATCCCCTTCTTTCCAACCAGG TGCGCCCCTGCCGCCCCGCTGGTCCCTACGCCGGGCTCTGGGGGATCCCCTTCTTTCCAACCAGG A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:19237498..19237810 26863196 MeRIP-seq:(Medium) rs987547299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17080547,Human_RBP_ID_26781559 RMVar_hsa_circ_182564,RMVar_hsa_circ_110734,RMVar_hsa_circ_119994,RMVar_hsa_circ_182565 60448 RMVar_ID_60448 Human_SNP_ID_619449775 m1A Human chr17 - 19271255 19271255 19271255 GCCTCCTCAGAACCCATCAGGCACTCTCTATCAACGTCACCAGCTGTCATCTGGAACAGAGCCCC GCCTCCTCAGAACCCATCAGGCACTCTCTATCGACGTCACCAGCTGTCATCTGGAACAGAGCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19271249..19271386 26863196 MeRIP-seq:(Medium) rs374844817 Functional Loss SNV dbSNP153 33..33 33 - - - 60449 RMVar_ID_60449 Human_SNP_ID_619454101 m1A Human chr17 + 19288544 19288544 19288544 GCCTTGTGGAGGTTGGAAAGAGCCTTCCAGGCAGAAGGGCAGCTGTGCAAAGGCCCTGAGGTGGG GCCTTGTGGAGGTTGGAAAGAGCCTTCCAGGCCGAAGGGCAGCTGTGCAAAGGCCCTGAGGTGGG A C EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19288506..19288614 26863196 MeRIP-seq:(Medium) rs1204928170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9069659 RMVar_hsa_circ_110734,RMVar_hsa_circ_182565,RMVar_hsa_circ_362802,RMVar_hsa_circ_314538,RMVar_hsa_circ_37998,RMVar_hsa_circ_70095,RMVar_hsa_circ_182566,RMVar_hsa_circ_86632 60450 RMVar_ID_60450 Human_SNP_ID_619466338 m1A Human chr17 + 19336027 19336027 19336027 CCCCTCTCTGGTTCCAGAAGATTACCCTTCGCACCGGCACAGGAGAGATCTTAAATGGTCTCTGG CCCCTCTCTGGTTCCAGAAGATTACCCTTCGCGCCGGCACAGGAGAGATCTTAAATGGTCTCTGG A G EPN2 Ensembl:ENSG00000072134 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:19335980..19336167 32194978 MeRIP-seq:(Medium) rs1407016558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17886709 RMVar_hsa_circ_182566,RMVar_hsa_circ_86632,RMVar_hsa_circ_103375,RMVar_hsa_circ_182571 60451 RMVar_ID_60451 Human_SNP_ID_619466467 m1A Human chr17 + 19336463 19336463 19336463 ACAGCCACTGGGCCACCGGGACCCAAGAAGACAGCCCCCTGCCCCATCTTCTGGCACAGGCCATC ACAGCCACTGGGCCACCGGGACCCAAGAAGACGGCCCCCTGCCCCATCTTCTGGCACAGGCCATC A G EPN2 Ensembl:ENSG00000072134 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:19336415..19336615 32194978 MeRIP-seq:(Medium) rs1402080329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484696 RMVar_hsa_circ_182566,RMVar_hsa_circ_86632,RMVar_hsa_circ_103375,RMVar_hsa_circ_182571 60452 RMVar_ID_60452 Human_SNP_ID_619467985 m1A Human chr17 - 19341885 19341885 19341885 CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCAACCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCAGCCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA T C B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19341834..19341968 26863196 MeRIP-seq:(Medium) rs755124474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 60453 RMVar_ID_60453 Human_SNP_ID_619467986 m1A Human chr17 - 19341885 19341885 19341885 CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCAACCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCACCCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA T G B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19341834..19341968 26863196 MeRIP-seq:(Medium) rs755124474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 60454 RMVar_ID_60454 Human_SNP_ID_619469543 m1A Human chr17 - 19347326 19347326 19347326 CTCTGTCTGCAAAAACATTTGTTTCAGGCACAAAAGGACCATCCCCATGTTTGTCCCAGAATCTA CTCTGTCTGCAAAAACATTTGTTTCAGGCACAGAAGGACCATCCCCATGTTTGTCCCAGAATCTA T C B9D1 Ensembl:ENSG00000108641 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:19347251..19347325 32194978 MeRIP-seq:(Medium) rs1430578855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1790434,Human_Splice_Rec_1790435,Human_Splice_Rec_1790446,Human_Splice_Rec_1790447,Human_Splice_Rec_1790458,Human_Splice_Rec_1790459,Human_Splice_Rec_1790470,Human_Splice_Rec_1790471,Human_Splice_Rec_1790482,Human_Splice_Rec_1790483,Human_Splice_Rec_1790492,Human_Splice_Rec_1790493,Human_Splice_Rec_1790502,Human_Splice_Rec_1790503,Human_Splice_Rec_1790514,Human_Splice_Rec_1790515,Human_Splice_Rec_1790520,Human_Splice_Rec_1790521,Human_Splice_Rec_1790532,Human_Splice_Rec_1790533,Human_Splice_Rec_1790544,Human_Splice_Rec_1790545,Human_Splice_Rec_1790556,Human_Splice_Rec_1790557,Human_Splice_Rec_1790566,Human_Splice_Rec_1790567,Human_Splice_Rec_1790576,Human_Splice_Rec_1790577,Human_Splice_Rec_1790586,Human_Splice_Rec_1790594 RMVar_hsa_circ_117382,RMVar_hsa_circ_105448,RMVar_hsa_circ_182572,RMVar_hsa_circ_182573 60455 RMVar_ID_60455 Human_SNP_ID_619473041 m1A Human chr17 - 19362578 19362578 19362578 GCGCGGCCTAGGTGGGTCCCCCCGGCACCCCCAGACCTGCCATGGCGACCGCGAGTCCTAGCGTC GCGCGGCCTAGGTGGGTCCCCCCGGCACCCCCGGACCTGCCATGGCGACCGCGAGTCCTAGCGTC T C B9D1 Ensembl:ENSG00000108641 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19362443..19362671 26863196 MeRIP-seq:(Medium) rs1381795986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465213,Human_RBP_ID_5187119,Human_RBP_ID_23714892 Human_Splice_Rec_1790427,Human_Splice_Rec_1790451,Human_Splice_Rec_1790463,Human_Splice_Rec_1790475,Human_Splice_Rec_1790485,Human_Splice_Rec_1790495,Human_Splice_Rec_1790537,Human_Splice_Rec_1790559,Human_Splice_Rec_1790569,Human_Splice_Rec_1790579 60456 RMVar_ID_60456 Human_SNP_ID_619473067 m1A Human chr17 + 19362598 19362598 19362598 CCATGGCAGGTCTGGGGGTGCCGGGGGGACCCACCTAGGCCGCGCGCGGTTGCTAAGAGACGCCG CCATGGCAGGTCTGGGGGTGCCGGGGGGACCCCCCTAGGCCGCGCGCGGTTGCTAAGAGACGCCG A C lnc-MAPK7-2 RNACentral:URS00008BEC78 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19362552..19362685 26863196 MeRIP-seq:(Medium) rs1420733330 Functional Loss SNV dbSNP153 33..33 33 - - - 60457 RMVar_ID_60457 Human_SNP_ID_619473110 m1A Human chr17 + 19362666 19362666 19362666 TTGCCCTAGAAACAGACGGCGTAGCGCGCAGGACACGTTTCTTGGCAGCGACACCTTCGCGAAGG TTGCCCTAGAAACAGACGGCGTAGCGCGCAGGGCACGTTTCTTGGCAGCGACACCTTCGCGAAGG A G lnc-MAPK7-2 RNACentral:URS00008BEC78 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19362457..19362700 26863196 MeRIP-seq:(Medium) rs1412136257 Functional Loss SNV dbSNP153 33..33 33 - - - 60458 RMVar_ID_60458 Human_SNP_ID_619476899 m1A Human chr17 - 19378544 19378540 19378544 CCAGCGCGGGGGTCTCCGAGGGTGGCTCACTTACTTGTTCAAAGGCCGCAGCCACCACCTCAGCG CCAGCGCGGGGGTCTCCGAGGGTGGCTCACTT____GTTCAAAGGCCGCAGCCACCACCTCAGCG CAAGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:19378504..19378594;chr17:19378520..19378672;chr17:19378494..19378655 26863196 MeRIP-seq:(Medium) rs1176730144 Functional Loss DEL dbSNP153 33..36 33 - - - 60459 RMVar_ID_60459 Human_SNP_ID_619477029 m1A Human chr17 + 19378972 19378972 19378972 TCTGCGGAGCCCCCCGGGCCCGTGAAGGCCGAACCCGCCCACACCGCTGCCTCTGTAGCGGCCAA TCTGCGGAGCCCCCCGGGCCCGTGAAGGCCGATCCCGCCCACACCGCTGCCTCTGTAGCGGCCAA A T MAPK7 Ensembl:ENSG00000166484 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:19378820..19378971 32194978 MeRIP-seq:(Medium) rs747827826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1790620,Human_Splice_Rec_1790646,Human_Splice_Rec_1790658,Human_Splice_Rec_1790664,Human_Splice_Rec_1790670,Human_Splice_Rec_1790676,Human_Splice_Rec_1790688,Human_Splice_Rec_1790694,Human_Splice_Rec_1790706 60460 RMVar_ID_60460 Human_SNP_ID_619477041 m1A Human chr17 - 19379010 19378998 19379010 TCACATCGAAGGAGCGGGCTTTAAGCAGGGCCAGGTTCTTGGCCGCTACAGAGGCAGCGGTGTGG TCACATCGAAGGAGCGGGCTTTAAGCAGGGCC____________GCTACAGAGGCAGCGGTGTGG CGGCCAAGAACCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19378867..19379022 26863196 MeRIP-seq:(Medium) rs771836793 Functional Loss DEL dbSNP153 33..44 33 - - - 60461 RMVar_ID_60461 Human_SNP_ID_619478145 m1A Human chr17 + 19382076 19382076 19382076 CCAGCCCTCACCTCTGTGCCGGCCCCTGCCCCAGCGCCAACGCCAACCCCAACCCCAGTCCAACC CCAGCCCTCACCTCTGTGCCGGCCCCTGCCCCGGCGCCAACGCCAACCCCAACCCCAGTCCAACC A G MAPK7 Ensembl:ENSG00000166484 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:19382025..19382360;chr17:19382027..19382357 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_133807,Human_RBP_ID_5129499,Human_RBP_ID_17080549,Human_RBP_ID_18942924 60462 RMVar_ID_60462 Human_SNP_ID_619478599 m1A Human chr17 + 19383193 19383193 19383193 CCCTGCAGCGTGAGATCCAGATGGACTCCCCAATGCTGCTGGCTGACCTGCCTGACCTCCAGGAC CCCTGCAGCGTGAGATCCAGATGGACTCCCCAGTGCTGCTGGCTGACCTGCCTGACCTCCAGGAC A G MAPK7 Ensembl:ENSG00000166484 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:19382117..19383344 32194978 MeRIP-seq:(Medium) rs757807560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27449554 60463 RMVar_ID_60463 Human_SNP_ID_619494434 m1A Human chr17 - 19446686 19446686 19446686 CCAAGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGATAAGGAGTGGATGCCCGTCACCAAGTTGG CCAAGGCCGCGGAGCTCGCGGAGGCAAGGCCGGGGATAAGGAGTGGATGCCCGTCACCAAGTTGG T C RPS2P46,AC004448.2 Ensembl:ENSG00000189343,Ensembl:ENSG00000235979 Pseudogene,lincRNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs974803327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5649047,Human_RBP_ID_17379054 Human_miRNA_ID_1880640 60464 RMVar_ID_60464 Human_SNP_ID_619494497 m1A Human chr17 - 19446800 19446800 19446800 AGCGGGGGGGCCCGGAGGCCCTGGTGGCCCTGAGATGGGGAACCGCGGTGGCTTCCGCGGAGGTT AGCGGGGGGGCCCGGAGGCCCTGGTGGCCCTGGGATGGGGAACCGCGGTGGCTTCCGCGGAGGTT T C RPS2P46,AC004448.2 Ensembl:ENSG00000189343,Ensembl:ENSG00000235979 Pseudogene,lincRNA exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1298923414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484728,Human_RBP_ID_9069704,Human_RBP_ID_18926717,Human_RBP_ID_21976519,Human_RBP_ID_22803418 Human_miRNA_ID_1852595,Human_miRNA_ID_1870129,Human_miRNA_ID_1896450 60465 RMVar_ID_60465 Human_SNP_ID_619494501 m1A Human chr17 - 19446817 19446817 19446817 GCGGATGACGCCGGTGCAGCGGGGGGGCCCGGAGGCCCTGGTGGCCCTGAGATGGGGAACCGCGG GCGGATGACGCCGGTGCAGCGGGGGGGCCCGGGGGCCCTGGTGGCCCTGAGATGGGGAACCGCGG T C RPS2P46,AC004448.2 Ensembl:ENSG00000189343,Ensembl:ENSG00000235979 Pseudogene,lincRNA exon,intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr17:19446697..19446829;chr17:19446687..19446828 26863196 MeRIP-seq:(Medium) rs1444740603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237342,Human_RBP_ID_484728,Human_RBP_ID_4469055,Human_RBP_ID_5187910,Human_RBP_ID_8253945,Human_RBP_ID_8825904,Human_RBP_ID_9069704,Human_RBP_ID_12919162,Human_RBP_ID_17673418,Human_RBP_ID_18926717,Human_RBP_ID_21960012,Human_RBP_ID_21976519,Human_RBP_ID_23128956,Human_RBP_ID_26956466,Human_RBP_ID_27250922 Human_miRNA_ID_1852595,Human_miRNA_ID_1870129,Human_miRNA_ID_1870130 60466 RMVar_ID_60466 Human_SNP_ID_619509957 m1A Human chr17 + 19508236 19508236 19508236 CGTCTGACTCCAGATCAGAAGGTTGCGTGTTCAAGTCACGTCGGGGTCAAGGTTGGGTTTTTTTT CGTCTGACTCCAGATCAGAAGGTTGCGTGTTCCAGTCACGTCGGGGTCAAGGTTGGGTTTTTTTT A C SLC47A1 Ensembl:ENSG00000142494 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1288689748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51128,Human_RBP_ID_484737,Human_RBP_ID_822898,Human_RBP_ID_1180546,Human_RBP_ID_1367335,Human_RBP_ID_1547117,Human_RBP_ID_1850672,Human_RBP_ID_3514576,Human_RBP_ID_5184415,Human_RBP_ID_5259916,Human_RBP_ID_5275033,Human_RBP_ID_5419892,Human_RBP_ID_5441201,Human_RBP_ID_5466193,Human_RBP_ID_5496642,Human_RBP_ID_6567529,Human_RBP_ID_8253221,Human_RBP_ID_8446240,Human_RBP_ID_8814068,Human_RBP_ID_9424662,Human_RBP_ID_9847917,Human_RBP_ID_10483669,Human_RBP_ID_12919227,Human_RBP_ID_17610203,Human_RBP_ID_17670047,Human_RBP_ID_17693532,Human_RBP_ID_18200112,Human_RBP_ID_18208101,Human_RBP_ID_18289580,Human_RBP_ID_18438501,Human_RBP_ID_18530499,Human_RBP_ID_18545431,Human_RBP_ID_18691117,Human_RBP_ID_18943916,Human_RBP_ID_20186490,Human_RBP_ID_22055852,Human_RBP_ID_22370830,Human_RBP_ID_22544897,Human_RBP_ID_22803427,Human_RBP_ID_22960035,Human_RBP_ID_23110443,Human_RBP_ID_23114533,Human_RBP_ID_23128959,Human_RBP_ID_23714956,Human_RBP_ID_24552536,Human_RBP_ID_25255667,Human_RBP_ID_26640230,Human_RBP_ID_26749046,Human_RBP_ID_26758235,Human_RBP_ID_26956477,Human_RBP_ID_27157081,Human_RBP_ID_27662289,Human_RBP_ID_27838392 60467 RMVar_ID_60467 Human_SNP_ID_619509958 m1A Human chr17 + 19508236 19508236 19508236 CGTCTGACTCCAGATCAGAAGGTTGCGTGTTCAAGTCACGTCGGGGTCAAGGTTGGGTTTTTTTT CGTCTGACTCCAGATCAGAAGGTTGCGTGTTCGAGTCACGTCGGGGTCAAGGTTGGGTTTTTTTT A G SLC47A1 Ensembl:ENSG00000142494 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1288689748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51128,Human_RBP_ID_484737,Human_RBP_ID_822898,Human_RBP_ID_1180546,Human_RBP_ID_1367335,Human_RBP_ID_1547117,Human_RBP_ID_1850672,Human_RBP_ID_3514576,Human_RBP_ID_5184415,Human_RBP_ID_5259916,Human_RBP_ID_5275033,Human_RBP_ID_5419892,Human_RBP_ID_5441201,Human_RBP_ID_5466193,Human_RBP_ID_5496642,Human_RBP_ID_6567529,Human_RBP_ID_8253221,Human_RBP_ID_8446240,Human_RBP_ID_8814068,Human_RBP_ID_9424662,Human_RBP_ID_9847917,Human_RBP_ID_10483669,Human_RBP_ID_12919227,Human_RBP_ID_17610203,Human_RBP_ID_17670047,Human_RBP_ID_17693532,Human_RBP_ID_18200112,Human_RBP_ID_18208101,Human_RBP_ID_18289580,Human_RBP_ID_18438501,Human_RBP_ID_18530499,Human_RBP_ID_18545431,Human_RBP_ID_18691117,Human_RBP_ID_18943916,Human_RBP_ID_20186490,Human_RBP_ID_22055852,Human_RBP_ID_22370830,Human_RBP_ID_22544897,Human_RBP_ID_22803427,Human_RBP_ID_22960035,Human_RBP_ID_23110443,Human_RBP_ID_23114533,Human_RBP_ID_23128959,Human_RBP_ID_23714956,Human_RBP_ID_24552536,Human_RBP_ID_25255667,Human_RBP_ID_26640230,Human_RBP_ID_26749046,Human_RBP_ID_26758235,Human_RBP_ID_26956477,Human_RBP_ID_27157081,Human_RBP_ID_27662289,Human_RBP_ID_27838392 60468 RMVar_ID_60468 Human_SNP_ID_619518843 m1A Human chr17 - 19542346 19542346 19542346 GAACGGGAAGGGACGTGAGTGACCACCATTGCAGGGAAGCCTGGGGCCCCAAGTGTGACCCCGAC GAACGGGAAGGGACGTGAGTGACCACCATTGCTGGGAAGCCTGGGGCCCCAAGTGTGACCCCGAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19542345..19546477 26863196 MeRIP-seq:(Medium) rs1442280165 Functional Loss SNV dbSNP153 33..33 33 - - - 60469 RMVar_ID_60469 Human_SNP_ID_619533513 m1A Human chr17 + 19601330 19601330 19601330 ATGAAGAGGCGGATATAAGACGAGAAGACCCTATGGAGCTTTAATTTATTAATGCAAATAAAAAC ATGAAGAGGCGGATATAAGACGAGAAGACCCTGTGGAGCTTTAATTTATTAATGCAAATAAAAAC A G AC025627.3 Ensembl:ENSG00000266179 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:19601317..19601407 26863196 MeRIP-seq:(Medium) rs1567585712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237390,Human_RBP_ID_819947,Human_RBP_ID_5238039,Human_RBP_ID_9341043,Human_RBP_ID_9883262,Human_RBP_ID_13220896,Human_RBP_ID_17189851,Human_RBP_ID_17207256,Human_RBP_ID_17380339,Human_RBP_ID_18208005,Human_RBP_ID_18470003,Human_RBP_ID_18531306 Human_miRNA_ID_1911200 60470 RMVar_ID_60470 Human_SNP_ID_619544434 m1A Human chr17 + 19648815 19648815 19648815 GACTCAGCGGGCGTGGAGGTCGCGGCTGAGCGAGCGAGCCCTGGGCGAGTGAATTGTGGCTGTGG GACTCAGCGGGCGTGGAGGTCGCGGCTGAGCGGGCGAGCCCTGGGCGAGTGAATTGTGGCTGTGG A G ALDH3A2 Ensembl:ENSG00000072210 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19648751..19649091 26863196 MeRIP-seq:(Medium) rs1159464571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764425,Human_RBP_ID_4410635,Human_RBP_ID_18419556 Human_Splice_Rec_1791233,Human_Splice_Rec_1791315,Human_Splice_Rec_1791339 RMVar_hsa_circ_90158,RMVar_hsa_circ_182585,RMVar_hsa_circ_182584 60471 RMVar_ID_60471 Human_SNP_ID_619544444 m1A Human chr17 - 19648824 19648824 19648824 ACCGTCAACCCACAGCCACAATTCACTCGCCCAGGGCTCGCTCGCTCAGCCGCGACCTCCACGCC ACCGTCAACCCACAGCCACAATTCACTCGCCCTGGGCTCGCTCGCTCAGCCGCGACCTCCACGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:19648776..19648975;chr17:19648776..19649080 26863196 MeRIP-seq:(Medium) rs1281223625 Functional Loss SNV dbSNP153 33..33 33 - - - 60472 RMVar_ID_60472 Human_SNP_ID_619544445 m1A Human chr17 - 19648824 19648824 19648824 ACCGTCAACCCACAGCCACAATTCACTCGCCCAGGGCTCGCTCGCTCAGCCGCGACCTCCACGCC ACCGTCAACCCACAGCCACAATTCACTCGCCCCGGGCTCGCTCGCTCAGCCGCGACCTCCACGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:19648776..19648975;chr17:19648776..19649080 26863196 MeRIP-seq:(Medium) rs1281223625 Functional Loss SNV dbSNP153 33..33 33 - - - 60473 RMVar_ID_60473 Human_SNP_ID_619569277 m1A Human chr17 + 19744934 19744932 19744934 CCCCTCCCCCCACGCCCCATCGCATGGCCCCGACACTGGCAGAAGGCGGCCGCCCAGCCTGAGCA CCCCTCCCCCCACGCCCCATCGCATGGCCCC__CACTGGCAGAAGGCGGCCGCCCAGCCTGAGCA CGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19744930..19745481 26863196 MeRIP-seq:(Medium) rs1567655881 Functional Loss DEL dbSNP153 32..33 33 - - - 60474 RMVar_ID_60474 Human_SNP_ID_619569281 m1A Human chr17 + 19744934 19744934 19744934 CCCCTCCCCCCACGCCCCATCGCATGGCCCCGACACTGGCAGAAGGCGGCCGCCCAGCCTGAGCA CCCCTCCCCCCACGCCCCATCGCATGGCCCCGCCACTGGCAGAAGGCGGCCGCCCAGCCTGAGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19744930..19745481 26863196 MeRIP-seq:(Medium) rs1195557490 Functional Loss SNV dbSNP153 33..33 33 - - - 60475 RMVar_ID_60475 Human_SNP_ID_619569284 m1A Human chr17 + 19744942 19744942 19744942 CCCACGCCCCATCGCATGGCCCCGACACTGGCAGAAGGCGGCCGCCCAGCCTGAGCACCTTGTGC CCCACGCCCCATCGCATGGCCCCGACACTGGCTGAAGGCGGCCGCCCAGCCTGAGCACCTTGTGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:19744937..19745026 26863196 MeRIP-seq:(Medium) rs778633741 Functional Loss SNV dbSNP153 33..33 33 - - - 60476 RMVar_ID_60476 Human_SNP_ID_619569443 m1A Human chr17 - 19745273 19745273 19745273 GTCTGAGTGAGGGGCGGGAGAGGAGGCGAGGCAGAAAGTGGACCTTCCAGCGGAAAGGCCATTTT GTCTGAGTGAGGGGCGGGAGAGGAGGCGAGGCGGAAAGTGGACCTTCCAGCGGAAAGGCCATTTT T C ALDH3A1 Ensembl:ENSG00000108602 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:19745268..19745354 26863196 MeRIP-seq:(Medium) rs1410015562 Functional Loss SNV dbSNP153 33..33 33 - - - 60477 RMVar_ID_60477 Human_SNP_ID_619601423 m1A Human chr17 - 19867887 19867861 19867887 TAGCGCGCGCGAGGGCGTTGGGCGCCGCCGCGAGGCGGGGAAGCGCGGGGCCGCGGCGGTGCGGG TAGCGCGCGCGAGGGCGTTGGGCGCCGCCGCG__________________________GTGCGGG CCGCCGCGGCCCCGCGCTTCCCCGCCT C ULK2 Ensembl:ENSG00000083290 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr17:19867610..19867923;chr17:19867333..19867915 26863196 MeRIP-seq:(Medium) rs1158917244 Functional Loss DEL dbSNP153 33..58 33 - - - 60478 RMVar_ID_60478 Human_SNP_ID_619601426 m1A Human chr17 - 19867887 19867864 19867887 TAGCGCGCGCGAGGGCGTTGGGCGCCGCCGCGAGGCGGGGAAGCGCGGGGCCGCGGCGGTGCGGG TAGCGCGCGCGAGGGCGTTGGGCGCCGCCGCG_______________________GCGGTGCGGG CCGCGGCCCCGCGCTTCCCCGCCT C ULK2 Ensembl:ENSG00000083290 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr17:19867610..19867923;chr17:19867333..19867915 26863196 MeRIP-seq:(Medium) rs1361924030 Functional Loss DEL dbSNP153 33..55 33 - - - 60479 RMVar_ID_60479 Human_SNP_ID_619601435 m1A Human chr17 - 19867879 19867879 19867879 GCGAGGGCGTTGGGCGCCGCCGCGAGGCGGGGAAGCGCGGGGCCGCGGCGGTGCGGGTTCTAGGG GCGAGGGCGTTGGGCGCCGCCGCGAGGCGGGGGAGCGCGGGGCCGCGGCGGTGCGGGTTCTAGGG T C ULK2 Ensembl:ENSG00000083290 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19867350..19867939 26863196 MeRIP-seq:(Medium) rs1206024446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4410808 60480 RMVar_ID_60480 Human_SNP_ID_619611192 m1A Human chr17 - 19905269 19905269 19905269 GACTGCCTCCCCCATTCTTTGCTGTGAGCTGGAAAGTGTGCAGTTGGTCGTCTTTCTTCTCCTTT GACTGCCTCCCCCATTCTTTGCTGTGAGCTGGGAAGTGTGCAGTTGGTCGTCTTTCTTCTCCTTT T C AKAP10 Ensembl:ENSG00000108599 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:19904801..19905351 32194978 MeRIP-seq:(Medium) rs1339722172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143761,Human_RBP_ID_12920033,Human_RBP_ID_23715162 60481 RMVar_ID_60481 Human_SNP_ID_619617886 m1A Human chr17 + 19931840 19931840 19931840 AGACGCAGAGCTGTCAGAACTCCCTGGGTGAGACTCATCAGGAGGGCCAACAGAGCCAGGAGCAG AGACGCAGAGCTGTCAGAACTCCCTGGGTGAGTCTCATCAGGAGGGCCAACAGAGCCAGGAGCAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:19924443..19936003 32194978 MeRIP-seq:(Medium) rs375240721 Functional Loss SNV dbSNP153 33..33 33 - - - 60482 RMVar_ID_60482 Human_SNP_ID_619688153 m1A Human chr17 - 20204475 20204474 20204475 TTTGTGGAAGGGGTCCTCAGGTGTTTCGTAGGAGTGGGAGTGTTGGAAGAAGTTGGACTGGACAC TTTGTGGAAGGGGTCCTCAGGTGTTTCGTAGG_GTGGGAGTGTTGGAAGAAGTTGGACTGGACAC CT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:20204426..20204525 26863196 MeRIP-seq:(Medium) rs1370989721 Functional Loss DEL dbSNP153 33..33 33 - - - 60483 RMVar_ID_60483 Human_SNP_ID_619688156 m1A Human chr17 - 20204475 20204475 20204475 TTTGTGGAAGGGGTCCTCAGGTGTTTCGTAGGAGTGGGAGTGTTGGAAGAAGTTGGACTGGACAC TTTGTGGAAGGGGTCCTCAGGTGTTTCGTAGGTGTGGGAGTGTTGGAAGAAGTTGGACTGGACAC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:20204426..20204525 26863196 MeRIP-seq:(Medium) rs778743497 Functional Loss SNV dbSNP153 33..33 33 - - - 60484 RMVar_ID_60484 Human_SNP_ID_619688382 m1A Human chr17 + 20205047 20205047 20205047 TTCTTTGTCGCCAGATGCTTCCGACTTTGAGCACATTACAGCAGAGACACCCTCAAGGCCCCTGT TTCTTTGTCGCCAGATGCTTCCGACTTTGAGCGCATTACAGCAGAGACACCCTCAAGGCCCCTGT A G SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:20205026..20205050 26863196 MeRIP-seq:(Medium) rs1422606730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1006646,Human_RBP_ID_2496809,Human_RBP_ID_3548243,Human_RBP_ID_5098131,Human_RBP_ID_5576885,Human_RBP_ID_8193931,Human_RBP_ID_26812013,Human_RBP_ID_27449634 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182685,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_182689,RMVar_hsa_circ_312205,RMVar_hsa_circ_330276,RMVar_hsa_circ_340270,RMVar_hsa_circ_337476,RMVar_hsa_circ_326157,RMVar_hsa_circ_294190,RMVar_hsa_circ_302130,RMVar_hsa_circ_271270,RMVar_hsa_circ_182687,RMVar_hsa_circ_182688,RMVar_hsa_circ_182686,RMVar_hsa_circ_182684 60485 RMVar_ID_60485 Human_SNP_ID_619695542 m1A Human chr17 + 20232351 20232351 20232351 GGAGGAGGAGAAGAATGCCCGGTTGCAGAAGGAGCTGGGGGATGTGCAGGGCCACGGCAGGGTGG GGAGGAGGAGAAGAATGCCCGGTTGCAGAAGGTGCTGGGGGATGTGCAGGGCCACGGCAGGGTGG A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:20232326..20232350 26863196 MeRIP-seq:(Medium) rs1197186385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549108,Human_RBP_ID_5098139,Human_RBP_ID_5579330,Human_RBP_ID_6568669,Human_RBP_ID_23715419,Human_RBP_ID_26331390,Human_RBP_ID_27813513 Human_Splice_Rec_1792319,Human_Splice_Rec_1792333,Human_Splice_Rec_1792397,Human_Splice_Rec_1792411,Human_Splice_Rec_1792449,Human_Splice_Rec_1792479,Human_Splice_Rec_1792489,Human_Splice_Rec_1792497 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_182689,RMVar_hsa_circ_330276,RMVar_hsa_circ_340270,RMVar_hsa_circ_326157,RMVar_hsa_circ_294190,RMVar_hsa_circ_302130,RMVar_hsa_circ_182687,RMVar_hsa_circ_182688,RMVar_hsa_circ_182686,RMVar_hsa_circ_182690,RMVar_hsa_circ_11564,RMVar_hsa_circ_305730,RMVar_hsa_circ_371077,RMVar_hsa_circ_316155,RMVar_hsa_circ_293838,RMVar_hsa_circ_182691,RMVar_hsa_circ_182694,RMVar_hsa_circ_182692,RMVar_hsa_circ_287577,RMVar_hsa_circ_300199,RMVar_hsa_circ_182693,RMVar_hsa_circ_99026 60486 RMVar_ID_60486 Human_SNP_ID_619699118 m1A Human chr17 - 20245865 20245865 20245865 AAAGATGGAGGACATCCCCATGGGAGAAAAAGACACAGAGGAAAACAGAACTGATGTGGAGAAAA AAAGATGGAGGACATCCCCATGGGAGAAAAAGGCACAGAGGAAAACAGAACTGATGTGGAGAAAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:20245860..20245975 26863196 MeRIP-seq:(Medium) rs1027871672 Functional Loss SNV dbSNP153 33..33 33 - - - 60487 RMVar_ID_60487 Human_SNP_ID_619699145 m1A Human chr17 - 20245935 20245935 20245935 GCAGCATCGACCTCAGAGGACTCTGGCTCTTCATCCACAGGTCTGCATGGCAAAGAGCAAATCAG GCAGCATCGACCTCAGAGGACTCTGGCTCTTCGTCCACAGGTCTGCATGGCAAAGAGCAAATCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:20245926..20246000 26863196 MeRIP-seq:(Medium) rs902817261 Functional Loss SNV dbSNP153 33..33 33 - - - 60488 RMVar_ID_60488 Human_SNP_ID_619719307 m1A Human chr17 + 20321670 20321670 20321670 GACAAGAGGGATAGGAAGAAGAGGTAATGGCCAGGCGAAGGATGCGGGCGCGCCGTCCTGTCGGG GACAAGAGGGATAGGAAGAAGAGGTAATGGCCTGGCGAAGGATGCGGGCGCGCCGTCCTGTCGGG A T AC004702.1,CCDC144CP Ensembl:ENSG00000263494,Ensembl:ENSG00000154898 lincRNA,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20321636..20321710 26863196 MeRIP-seq:(Medium) rs775826221 Functional Loss SNV dbSNP153 33..33 33 - - - 60489 RMVar_ID_60489 Human_SNP_ID_619731315 m1A Human chr17 - 20376344 20376344 20376344 AGAAGAAGAGAAGAAGAAAGATGCAAAAAAAAAAAGAGAGACAGATAAACAGAAGAAAATTGCAG AGAAGAAGAGAAGAAGAAAGATGCAAAAAAAAGAAGAGAGACAGATAAACAGAAGAAAATTGCAG T C UPF3AP2 Ensembl:ENSG00000214832 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20376311..20376380 26863196 MeRIP-seq:(Medium) rs985528137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901593,Human_RBP_ID_1546852,Human_RBP_ID_3548619,Human_RBP_ID_8826046 60490 RMVar_ID_60490 Human_SNP_ID_619731327 m1A Human chr17 - 20376362 20376362 20376362 CGGGAAGAGGAAAAAAGAAGAAGAAGAGAAGAAGAAAGATGCAAAAAAAAAAAGAGAGACAGATA CGGGAAGAGGAAAAAAGAAGAAGAAGAGAAGATGAAAGATGCAAAAAAAAAAAGAGAGACAGATA T A UPF3AP2 Ensembl:ENSG00000214832 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:20376303..20376392 26863196 MeRIP-seq:(Medium) rs879864206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901593,Human_RBP_ID_1546852,Human_RBP_ID_3548619 60491 RMVar_ID_60491 Human_SNP_ID_619766457 m1A Human chr17 + 20532793 20532791 20532794 GCGGCAAGAAAATGGAGAAGAGGCTGGGAAAGACGACGATTGGGAGAGGAGAAGAGGGTGGGAAG GCGGCAAGAAAATGGAGAAGAGGCTGGGAAA___GACGATTGGGAGAGGAGAAGAGGGTGGGAAG AGAC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:20532734..20532946 26863196 MeRIP-seq:(Medium) rs1312307201 Functional Loss DEL dbSNP153 32..34 33 - - - 60492 RMVar_ID_60492 Human_SNP_ID_619766459 m1A Human chr17 + 20532796 20532796 20532796 GCAAGAAAATGGAGAAGAGGCTGGGAAAGACGACGATTGGGAGAGGAGAAGAGGGTGGGAAGAAG GCAAGAAAATGGAGAAGAGGCTGGGAAAGACGGCGATTGGGAGAGGAGAAGAGGGTGGGAAGAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:20532721..20532962 26863196 MeRIP-seq:(Medium) rs1330034511 Functional Loss SNV dbSNP153 33..33 33 - - - 60493 RMVar_ID_60493 Human_SNP_ID_619766582 m1A Human chr17 + 20533119 20533118 20533119 AGACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGGA AGACTGAGGGGAAGAAAACGGTGGGGAAGGGG_AAAAAAACTGCGGGGGAGAAGAAGGTGCGGGA GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20533080..20533161 26863196 MeRIP-seq:(Medium) rs71305118 Functional Loss DEL dbSNP153 33..33 33 - - - 60494 RMVar_ID_60494 Human_SNP_ID_619766585 m1A Human chr17 + 20533119 20533119 20533119 AGACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGGA AGACTGAGGGGAAGAAAACGGTGGGGAAGGGGGAAAAAAACTGCGGGGGAGAAGAAGGTGCGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20533080..20533161 26863196 MeRIP-seq:(Medium) rs1362034474 Functional Loss SNV dbSNP153 33..33 33 - - - 60495 RMVar_ID_60495 Human_SNP_ID_619766586 m1A Human chr17 + 20533120 20533120 20533120 GACTGAGGGGAAGAAAACGGTGGGGAAGGGGAAAAAAAACTGCGGGGGAGAAGAAGGTGCGGGAA GACTGAGGGGAAGAAAACGGTGGGGAAGGGGAGAAAAAACTGCGGGGGAGAAGAAGGTGCGGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:20533076..20533169;chr17:20533065..20533188;chr17:20533059..20533178 26863196 MeRIP-seq:(Medium) rs1382111365 Functional Loss SNV dbSNP153 33..33 33 - - - 60496 RMVar_ID_60496 Human_SNP_ID_619766727 m1A Human chr17 - 20533434 20533434 20533434 TCTTCTCTCCCACCCATCTTTTTCCCCTCTCCATCTCTTTCCCCAAGGTCGTCTTCGCCGCTTTC TCTTCTCTCCCACCCATCTTTTTCCCCTCTCCTTCTCTTTCCCCAAGGTCGTCTTCGCCGCTTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:20533358..20533518;chr17:20533344..20533527 26863196 MeRIP-seq:(Medium) rs1364533535 Functional Loss SNV dbSNP153 33..33 33 - - - 60497 RMVar_ID_60497 Human_SNP_ID_619766728 m1A Human chr17 - 20533434 20533434 20533434 TCTTCTCTCCCACCCATCTTTTTCCCCTCTCCATCTCTTTCCCCAAGGTCGTCTTCGCCGCTTTC TCTTCTCTCCCACCCATCTTTTTCCCCTCTCCCTCTCTTTCCCCAAGGTCGTCTTCGCCGCTTTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:20533358..20533518;chr17:20533344..20533527 26863196 MeRIP-seq:(Medium) rs1364533535 Functional Loss SNV dbSNP153 33..33 33 - - - 60498 RMVar_ID_60498 Human_SNP_ID_619766750 m1A Human chr17 + 20533502 20533499 20533503 TGAGGCAGGGAACGAGGTGGGGAGGGGAAGAAAAAGGCAGAAAGACGGGCTGAGAAGAGTGCTGG TGAGGCAGGGAACGAGGTGGGGAGGGGAAG____AGGCAGAAAGACGGGCTGAGAAGAGTGCTGG GAAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20533282..20533643 26863196 MeRIP-seq:(Medium) rs1389212361 Functional Loss DEL dbSNP153 31..34 33 - - - 60499 RMVar_ID_60499 Human_SNP_ID_619766752 m1A Human chr17 + 20533502 20533502 20533502 TGAGGCAGGGAACGAGGTGGGGAGGGGAAGAAAAAGGCAGAAAGACGGGCTGAGAAGAGTGCTGG TGAGGCAGGGAACGAGGTGGGGAGGGGAAGAACAAGGCAGAAAGACGGGCTGAGAAGAGTGCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:20533282..20533643 26863196 MeRIP-seq:(Medium) rs1224801437 Functional Loss SNV dbSNP153 33..33 33 - - - 60500 RMVar_ID_60500 Human_SNP_ID_619889122 m1A Human chr17 + 20999949 20999949 20999949 TGCAGTGCTCACCACGAAGCCCAGGTCCACGGAGGGAGCCAAGGTCCACAGAGGGCCCCGGGGCC TGCAGTGCTCACCACGAAGCCCAGGTCCACGGCGGGAGCCAAGGTCCACAGAGGGCCCCGGGGCC A C AC087393.2,CCDC144NL-AS1 Ensembl:ENSG00000263986,Ensembl:ENSG00000233098 lincRNA,lincRNA exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:20999876..21000175 32194978 MeRIP-seq:(Medium) rs149886063 Functional Loss SNV dbSNP153 33..33 33 - - - 60501 RMVar_ID_60501 Human_SNP_ID_619889301 m1A Human chr17 + 21000627 21000627 21000627 CAGGGTCTGGCCAAACCCAGGCAGCTGCCAGAAAGCCTTCTGCACTCCGCAAGACACCCCAGTAA CAGGGTCTGGCCAAACCCAGGCAGCTGCCAGAGAGCCTTCTGCACTCCGCAAGACACCCCAGTAA A G CCDC144NL-AS1 Ensembl:ENSG00000233098 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21000576..21000650 32194978 MeRIP-seq:(Medium) rs1317861856 Functional Loss SNV dbSNP153 33..33 33 - - - 60502 RMVar_ID_60502 Human_SNP_ID_619889378 m1A Human chr17 - 21000918 21000918 21000918 AGCCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCACGCCAGGCTAATTTTTGTATTTTTAG AGCCTCCCAAGTAGCTGGGACTACAGGCATGCGCCACCACGCCAGGCTAATTTTTGTATTTTTAG T C USP22 Ensembl:ENSG00000124422 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1127815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_104605,RMVar_hsa_circ_101623,RMVar_hsa_circ_182719,RMVar_hsa_circ_81808,RMVar_hsa_circ_182720,RMVar_hsa_circ_182718 60503 RMVar_ID_60503 Human_SNP_ID_619889711 m1A Human chr17 + 21002100 21002100 21002100 CGAGGGACAGAACCCATCAGACACCGGCAGACACTGCATTTACTCCAGACTGAGATGACAGACAC CGAGGGACAGAACCCATCAGACACCGGCAGACGCTGCATTTACTCCAGACTGAGATGACAGACAC A G CCDC144NL-AS1 Ensembl:ENSG00000233098 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21002051..21002100 32194978 MeRIP-seq:(Medium) rs561902096 Functional Loss SNV dbSNP153 33..33 33 - - - 60504 RMVar_ID_60504 Human_SNP_ID_619889939 m1A Human chr17 - 21002766 21002766 21002766 CTGGGTGGGAGGAGCAGCGTACACCCGTCACCAGAACATCTCTTGTGTCATGACATGGGGGTGCA CTGGGTGGGAGGAGCAGCGTACACCCGTCACCGGAACATCTCTTGTGTCATGACATGGGGGTGCA T C USP22 Ensembl:ENSG00000124422 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21002715..21002802 26863196 MeRIP-seq:(Medium) rs780497278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1529369,Human_RBP_ID_1850965,Human_RBP_ID_3515096,Human_RBP_ID_4411155,Human_RBP_ID_5143128,Human_RBP_ID_5525427,Human_RBP_ID_8814227,Human_RBP_ID_23715924,Human_RBP_ID_26447974 Human_miRNA_ID_2600048 RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_104605,RMVar_hsa_circ_101623,RMVar_hsa_circ_182719,RMVar_hsa_circ_81808,RMVar_hsa_circ_182720,RMVar_hsa_circ_182718,RMVar_hsa_circ_182722 60505 RMVar_ID_60505 Human_SNP_ID_619892597 m1A Human chr17 - 21011202 21011202 21011202 CCTGAGCCCAGGGAGCGAGGGCAACGTGGTAAACGGGGAAAGCCACGTGTCGGGAACCACCACGC CCTGAGCCCAGGGAGCGAGGGCAACGTGGTAATCGGGGAAAGCCACGTGTCGGGAACCACCACGC T A USP22 Ensembl:ENSG00000124422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:21011120..21011351 26863196 MeRIP-seq:(Medium) rs950604115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236058,Human_RBP_ID_6569199,Human_RBP_ID_26332991 Human_Splice_Rec_1793099,Human_Splice_Rec_1793123,Human_Splice_Rec_1793151,Human_Splice_Rec_1793163 RMVar_hsa_circ_2515,RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_81808,RMVar_hsa_circ_182718,RMVar_hsa_circ_182722,RMVar_hsa_circ_317048,RMVar_hsa_circ_374685,RMVar_hsa_circ_310247,RMVar_hsa_circ_125521,RMVar_hsa_circ_108933,RMVar_hsa_circ_51758,RMVar_hsa_circ_182724,RMVar_hsa_circ_182726,RMVar_hsa_circ_182725,RMVar_hsa_circ_182723,RMVar_hsa_circ_372154,RMVar_hsa_circ_301801,RMVar_hsa_circ_378132,RMVar_hsa_circ_182729,RMVar_hsa_circ_324166,RMVar_hsa_circ_282847,RMVar_hsa_circ_103075,RMVar_hsa_circ_182734,RMVar_hsa_circ_182735,RMVar_hsa_circ_182733,RMVar_hsa_circ_14248,RMVar_hsa_circ_182737,RMVar_hsa_circ_97245,RMVar_hsa_circ_275750,RMVar_hsa_circ_114722,RMVar_hsa_circ_182738,RMVar_hsa_circ_182739 60506 RMVar_ID_60506 Human_SNP_ID_619892630 m1A Human chr17 + 21011329 21011329 21011329 GGTGGAGACTCCACTGGAAGCAGAGGGAAAACAATGGCTGTGAGGACTGACACCCACCCAGCTCC GGTGGAGACTCCACTGGAAGCAGAGGGAAAACTATGGCTGTGAGGACTGACACCCACCCAGCTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr17:21011326..21011430;chr17:21011326..21011375 26863196,32194978 MeRIP-seq:(Medium) rs772419289 Functional Loss SNV dbSNP153 33..33 33 - - - 60507 RMVar_ID_60507 Human_SNP_ID_619893841 m1A Human chr17 - 21015702 21015702 21015702 CACCCTCCACCAGGGCAGGATGTTTTCCTTGAAGGGGAAGGAAGCAAAGCGAGTGTATGCACTCG CACCCTCCACCAGGGCAGGATGTTTTCCTTGAGGGGGAAGGAAGCAAAGCGAGTGTATGCACTCG T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:21015699..21015849 26863196 MeRIP-seq:(Medium) rs778527371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362589,Human_RBP_ID_19078554,Human_RBP_ID_23256863 RMVar_hsa_circ_2515,RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_81808,RMVar_hsa_circ_182718,RMVar_hsa_circ_182722,RMVar_hsa_circ_374685,RMVar_hsa_circ_310247,RMVar_hsa_circ_125521,RMVar_hsa_circ_51758,RMVar_hsa_circ_182724,RMVar_hsa_circ_182725,RMVar_hsa_circ_182723,RMVar_hsa_circ_378132,RMVar_hsa_circ_324166,RMVar_hsa_circ_103075,RMVar_hsa_circ_182735,RMVar_hsa_circ_14248,RMVar_hsa_circ_182737,RMVar_hsa_circ_275750,RMVar_hsa_circ_114722,RMVar_hsa_circ_182738,RMVar_hsa_circ_182740,RMVar_hsa_circ_268517,RMVar_hsa_circ_337341,RMVar_hsa_circ_369578,RMVar_hsa_circ_182741 60508 RMVar_ID_60508 Human_SNP_ID_619901576 m1A Human chr17 - 21041987 21041987 21041987 TCGCGGCTGCCTCGGGGCCCGCGAGGAGCTGGAGGTGGAGGGCGGCAGGGGCTGGGGCCGGGGCG TCGCGGCTGCCTCGGGGCCCGCGAGGAGCTGGGGGTGGAGGGCGGCAGGGGCTGGGGCCGGGGCG T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21041976..21042121 26863196 MeRIP-seq:(Medium) rs1030164986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542801,Human_RBP_ID_8189513,Human_RBP_ID_8231994,Human_RBP_ID_17128666,Human_RBP_ID_17566792 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 60509 RMVar_ID_60509 Human_SNP_ID_619902044 m1A Human chr17 + 21042874 21042874 21042874 CAAGGCCCGGCCGCGCGCGGGGGGCGGCGGCGAGGGAGGCGAGGACGACGCCAGCGCGGCGTGGG CAAGGCCCGGCCGCGCGCGGGGGGCGGCGGCGCGGGAGGCGAGGACGACGCCAGCGCGGCGTGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21042826..21043000 26863196 MeRIP-seq:(Medium) rs960287518 Functional Loss SNV dbSNP153 33..33 33 - - - 60510 RMVar_ID_60510 Human_SNP_ID_619902045 m1A Human chr17 + 21042874 21042874 21042874 CAAGGCCCGGCCGCGCGCGGGGGGCGGCGGCGAGGGAGGCGAGGACGACGCCAGCGCGGCGTGGG CAAGGCCCGGCCGCGCGCGGGGGGCGGCGGCGGGGGAGGCGAGGACGACGCCAGCGCGGCGTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21042826..21043000 26863196 MeRIP-seq:(Medium) rs960287518 Functional Loss SNV dbSNP153 33..33 33 - - - 60511 RMVar_ID_60511 Human_SNP_ID_619902053 m1A Human chr17 - 21042903 21042903 21042903 TGGCCAGCCTGGCCAGCCGCCGAGCAGCCCCCACGCCGCGCTGGCGTCGTCCTCGCCTCCCTCGC TGGCCAGCCTGGCCAGCCGCCGAGCAGCCCCCGCGCCGCGCTGGCGTCGTCCTCGCCTCCCTCGC T C USP22 Ensembl:ENSG00000124422 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:21042858..21042971 26863196 MeRIP-seq:(Medium) rs1470494070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822283,Human_RBP_ID_4411262,Human_RBP_ID_9326522 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 60512 RMVar_ID_60512 Human_SNP_ID_619902057 m1A Human chr17 - 21042910 21042910 21042910 CGGGCCTTGGCCAGCCTGGCCAGCCGCCGAGCAGCCCCCACGCCGCGCTGGCGTCGTCCTCGCCT CGGGCCTTGGCCAGCCTGGCCAGCCGCCGAGCGGCCCCCACGCCGCGCTGGCGTCGTCCTCGCCT T C USP22 Ensembl:ENSG00000124422 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21042859..21042967 26863196 MeRIP-seq:(Medium) rs942099410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236067,Human_RBP_ID_822283,Human_RBP_ID_4411263,Human_RBP_ID_9326522 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 60513 RMVar_ID_60513 Human_SNP_ID_619902062 m1A Human chr17 + 21042926 21042917 21042926 AGCGCGGCGTGGGGGCTGCTCGGCGGCTGGCCAGGCTGGCCAAGGCCCGGGCGCCGAGAACAAAG AGCGCGGCGTGGGGGCTGCTCGGC_________GGCTGGCCAAGGCCCGGGCGCCGAGAACAAAG CGGCTGGCCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:21042776..21042978;chr17:21042826..21043025;chr17:21042733..21043032 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1048776231 Functional Loss DEL dbSNP153 25..33 33 - - - 60514 RMVar_ID_60514 Human_SNP_ID_619951767 m1A Human chr17 + 21242456 21242456 21242456 AGTCAGCTTCACTCCCACCCCAGCCCCAAGGCATCTCCTCGGAGAAGGCTCAGGCAGGTGGCCAA AGTCAGCTTCACTCCCACCCCAGCCCCAAGGCTTCTCCTCGGAGAAGGCTCAGGCAGGTGGCCAA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21242405..21242505 32194978 MeRIP-seq:(Medium) rs967526636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8446776 60515 RMVar_ID_60515 Human_SNP_ID_619951841 m1A Human chr17 - 21242693 21242693 21242693 CAACCGTACGTGCGGTTCACACATGTGAACACACAGGATGCAGTCTACAGGCGGGCTGGTGGTGG CAACCGTACGTGCGGTTCACACATGTGAACACGCAGGATGCAGTCTACAGGCGGGCTGGTGGTGG T C NATD1 Ensembl:ENSG00000274180 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21242604..21242704 32194978 MeRIP-seq:(Medium) rs750801575 Functional Loss SNV dbSNP153 33..33 33 - - - 60516 RMVar_ID_60516 Human_SNP_ID_619954787 m1A Human chr17 + 21253352 21253352 21253352 TCAGGCGCGCGGCGGGGCTGGAGCGCGGGCGCAGGCGGCAGGCGGTGGGGTAGTTACGGCCTGGG TCAGGCGCGCGGCGGGGCTGGAGCGCGGGCGCCGGCGGCAGGCGGTGGGGTAGTTACGGCCTGGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:21253284..21253418 26863196 MeRIP-seq:(Medium) rs974076613 Functional Loss SNV dbSNP153 33..33 33 - - - 60517 RMVar_ID_60517 Human_SNP_ID_619962717 m1A Human chr17 - 21284771 21284759 21284771 CGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGAGGACTGCGGCGGCGACTGCAGCAAGGACGAGT CGGCGGCGGCGGCGGCGGCGGCGACTGCGGCG____________GCGACTGCAGCAAGGACGAGT CCGCCGCAGTCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21284726..21285017 26863196 MeRIP-seq:(Medium) rs1200673824 Functional Loss DEL dbSNP153 33..44 33 - - - 60518 RMVar_ID_60518 Human_SNP_ID_619962724 m1A Human chr17 - 21284771 21284771 21284771 CGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGAGGACTGCGGCGGCGACTGCAGCAAGGACGAGT CGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGGGGACTGCGGCGGCGACTGCAGCAAGGACGAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21284726..21285017 26863196 MeRIP-seq:(Medium) rs902096969 Functional Loss SNV dbSNP153 33..33 33 - - - 60519 RMVar_ID_60519 Human_SNP_ID_619962728 m1A Human chr17 - 21284780 21284780 21284780 GAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGAGGACTGCGGCGGCGACTGCAGCA GAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGCGGCGAGGACTGCGGCGGCGACTGCAGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:21284754..21284924;chr17:21284739..21285013 26863196 MeRIP-seq:(Medium) rs1050368182 Functional Loss SNV dbSNP153 33..33 33 - - - 60520 RMVar_ID_60520 Human_SNP_ID_619966244 m1A Human chr17 + 21295087 21295087 21295087 GCAGCCTCTCTGAACTGGTGAAAGGCAAGACGACGTAGTAGCTAGGACAGTCACAGGGAAGAGCA GCAGCCTCTCTGAACTGGTGAAAGGCAAGACGGCGTAGTAGCTAGGACAGTCACAGGGAAGAGCA A G MAP2K3 Ensembl:ENSG00000034152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:21295084..21295243 26863196 MeRIP-seq:(Medium) rs1567661917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12928195 60521 RMVar_ID_60521 Human_SNP_ID_619967665 m1A Human chr17 + 21298478 21298478 21298478 CCTGCATGTCCAAGCCACCCGCACCCAACCCCACGTGAGTCTGCCTCAGTTTCTCCCTGGCTCAC CCTGCATGTCCAAGCCACCCGCACCCAACCCCCCGTGAGTCTGCCTCAGTTTCTCCCTGGCTCAC A C MAP2K3 Ensembl:ENSG00000034152 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21298401..21298500 32194978 MeRIP-seq:(Medium) rs1363198122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081806 Human_Splice_Rec_1793326,Human_Splice_Rec_1793327,Human_Splice_Rec_1793362,Human_Splice_Rec_1793366,Human_Splice_Rec_1793367,Human_Splice_Rec_1793372,Human_Splice_Rec_1793373,Human_Splice_Rec_1793380,Human_Splice_Rec_1793381,Human_Splice_Rec_1793402,Human_Splice_Rec_1793403,Human_Splice_Rec_1793422,Human_Splice_Rec_1793423,Human_Splice_Rec_1793434,Human_Splice_Rec_1793435,Human_Splice_Rec_1793458,Human_Splice_Rec_1793459,Human_Splice_Rec_1793482,Human_Splice_Rec_1793483 RMVar_hsa_circ_45356,RMVar_hsa_circ_104785,RMVar_hsa_circ_182767,RMVar_hsa_circ_355661,RMVar_hsa_circ_28497 60522 RMVar_ID_60522 Human_SNP_ID_619968620 m1A Human chr17 - 21300660 21300660 21300660 GGAGCCCTCCCAGCTGCCTCCAGGCCCTGCTCACCTTCACGGCCATGATGGTGCCGCTCTGGGCG GGAGCCCTCCCAGCTGCCTCCAGGCCCTGCTCCCCTTCACGGCCATGATGGTGCCGCTCTGGGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:21300613..21300698 26863196 MeRIP-seq:(Medium) rs770555695 Functional Loss SNV dbSNP153 33..33 33 - - - 60523 RMVar_ID_60523 Human_SNP_ID_619970269 m1A Human chr17 - 21304525 21304525 21304525 TCACGGCCATGTAGGGCTTGCAGCCGGCATCCATCGTCTTGGCCACAGAGTCCACCAAGTAGCCA TCACGGCCATGTAGGGCTTGCAGCCGGCATCCGTCGTCTTGGCCACAGAGTCCACCAAGTAGCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21304476..21311730 32194978 MeRIP-seq:(Medium) rs760085339 Functional Loss SNV dbSNP153 33..33 33 - - - 60524 RMVar_ID_60524 Human_SNP_ID_619973506 m1A Human chr17 + 21314803 21314803 21314803 TCCCCTGGCACTGGCAAACAGGGCCTCTGCGGAGCACACTGGCTCACCCAGTCCTGCCCGCCACC TCCCCTGGCACTGGCAAACAGGGCCTCTGCGGGGCACACTGGCTCACCCAGTCCTGCCCGCCACC A G MAP2K3 Ensembl:ENSG00000034152 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21314692..21314875 32194978 MeRIP-seq:(Medium) rs4021723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485114,Human_RBP_ID_6569921,Human_RBP_ID_23716158 Human_miRNA_ID_624704 GWAS_ID_7297 60525 RMVar_ID_60525 Human_SNP_ID_620032288 m1A Human chr17 - 21530516 21530516 21530516 GGGTAAAGCCTGGGGAATGCCAGCATTTAGAAAGAGGCCGCTGGAGATCAGAAAAGAGCAACAGG GGGTAAAGCCTGGGGAATGCCAGCATTTAGAAGGAGGCCGCTGGAGATCAGAAAAGAGCAACAGG T C LINC02693 Ensembl:ENSG00000212719 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:21530418..21530624 26863196 MeRIP-seq:(Medium) rs550159270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12928578 RMVar_hsa_circ_182769 60526 RMVar_ID_60526 Human_SNP_ID_620032290 m1A Human chr17 + 21530521 21530521 21530521 TGCTCTTTTCTGATCTCCAGCGGCCTCTTTCTAAATGCTGGCATTCCCCAGGCTTTACCCTGGGC TGCTCTTTTCTGATCTCCAGCGGCCTCTTTCTGAATGCTGGCATTCCCCAGGCTTTACCCTGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21530422..21530589 26863196 MeRIP-seq:(Medium) rs946753149 Functional Loss SNV dbSNP153 33..33 33 - - - 60527 RMVar_ID_60527 Human_SNP_ID_620101467 m1A Human chr17 + 21780417 21780417 21780417 CCCTCCCTCTCCTCTGACCCGGCCACCCAGGCACACAGCAGGCACAGCCCCACCTCAGGGCCTTT CCCTCCCTCTCCTCTGACCCGGCCACCCAGGCGCACAGCAGGCACAGCCCCACCTCAGGGCCTTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:21780394..21780576 26863196 MeRIP-seq:(Medium) rs1274611249 Functional Loss SNV dbSNP153 33..33 33 - - - 60528 RMVar_ID_60528 Human_SNP_ID_620171556 m1A Human chr17 + 21969675 21969675 21969675 CCCGAGTGGTGTGGAATGGAATGGAATGGAATAGAATGGAATGGAATGCAATCAACCAGAGTGGA CCCGAGTGGTGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATGCAATCAACCAGAGTGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21969662..21969780 26863196 MeRIP-seq:(Medium) rs1238592277 Functional Loss SNV dbSNP153 33..33 33 - - - 60529 RMVar_ID_60529 Human_SNP_ID_620171557 m1A Human chr17 + 21969675 21969675 21969675 CCCGAGTGGTGTGGAATGGAATGGAATGGAATAGAATGGAATGGAATGCAATCAACCAGAGTGGA CCCGAGTGGTGTGGAATGGAATGGAATGGAATTGAATGGAATGGAATGCAATCAACCAGAGTGGA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21969662..21969780 26863196 MeRIP-seq:(Medium) rs1238592277 Functional Loss SNV dbSNP153 33..33 33 - - - 60530 RMVar_ID_60530 Human_SNP_ID_620174524 m1A Human chr17 - 21976827 21976827 21976827 CCACTCCATTCCAATCCATTCCATTCCATTCCACTCCACTCGGGTTGATTCCATTCCTTTCCGTT CCACTCCATTCCAATCCATTCCATTCCATTCCCCTCCACTCGGGTTGATTCCATTCCTTTCCGTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21976825..21977145 26863196 MeRIP-seq:(Medium) rs1380017264 Functional Loss SNV dbSNP153 33..33 33 - - - 60531 RMVar_ID_60531 Human_SNP_ID_620182834 m1A Human chr17 + 21991626 21991626 21991626 AATCCGAGTGGAATGGAATGGAATGGAATAGAATGGAAGAGAATGGAATTGAATCCACCCGATTG AATCCGAGTGGAATGGAATGGAATGGAATAGAGTGGAAGAGAATGGAATTGAATCCACCCGATTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21991524..21991791 26863196 MeRIP-seq:(Medium) rs1330069745 Functional Loss SNV dbSNP153 33..33 33 - - - 60532 RMVar_ID_60532 Human_SNP_ID_620183020 m1A Human chr17 - 21991935 21991935 21991935 ATTCCATTCTACTCCATTCCATTCCATTCCATACCATTCCATTGCATTCCACTTGGGTTGATTCC ATTCCATTCTACTCCATTCCATTCCATTCCATTCCATTCCATTGCATTCCACTTGGGTTGATTCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21991849..21991974 26863196 MeRIP-seq:(Medium) rs1339131686 Functional Loss SNV dbSNP153 33..33 33 - - - 60533 RMVar_ID_60533 Human_SNP_ID_620183021 m1A Human chr17 - 21991935 21991935 21991935 ATTCCATTCTACTCCATTCCATTCCATTCCATACCATTCCATTGCATTCCACTTGGGTTGATTCC ATTCCATTCTACTCCATTCCATTCCATTCCATCCCATTCCATTGCATTCCACTTGGGTTGATTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:21991849..21991974 26863196 MeRIP-seq:(Medium) rs1339131686 Functional Loss SNV dbSNP153 33..33 33 - - - 60534 RMVar_ID_60534 Human_SNP_ID_620311720 m1A Human chr17 + 22521416 22521416 22521416 AATAAGACATCACGATGGATCACGGGTCTATTACCCTATTAATCAGTCACGGGAGCTCTCCATGC AATAAGACATCACGATGGATCACGGGTCTATTTCCCTATTAATCAGTCACGGGAGCTCTCCATGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:22521361..22521439 26863196 MeRIP-seq:(Medium) rs1379895626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26448064 60535 RMVar_ID_60535 Human_SNP_ID_620312687 m1A Human chr17 + 22524048 22524048 22524048 GTAAAGGTAGCATAATCACTTGTTCCTTAAATAGGGACTTGTCTGAATGGCTCCACGAGGGTTCA GTAAAGGTAGCATAATCACTTGTTCCTTAAATGGGGACTTGTCTGAATGGCTCCACGAGGGTTCA A G MTRNR2L1 Ensembl:ENSG00000256618 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:22523861..22524254 26863196 MeRIP-seq:(Medium) rs183519861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_201539,Human_RBP_ID_5237877,Human_RBP_ID_22357198,Human_RBP_ID_22443505,Human_RBP_ID_22543026,Human_RBP_ID_23256864,Human_RBP_ID_23276431 60536 RMVar_ID_60536 Human_SNP_ID_620312704 m1A Human chr17 - 22524083 22524083 22524083 CAGGTCAATTTCACTGGTTGAAAGTAAGAGACAGCTGAACCCTCGTGGAGCCATTCAGACAAGTC CAGGTCAATTTCACTGGTTGAAAGTAAGAGACGGCTGAACCCTCGTGGAGCCATTCAGACAAGTC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:22524017..22524159 26863410 MeRIP-seq:(Medium) rs1387554875 Functional Loss SNV dbSNP153 33..33 33 - - - 60537 RMVar_ID_60537 Human_SNP_ID_620312722 m1A Human chr17 + 22524131 22524131 22524131 CCAGTGAAATTGACCTGCCCGTGAAGAGGCGGACATAATACAACAAGACGAGAAGACCCTAAGGA CCAGTGAAATTGACCTGCCCGTGAAGAGGCGGCCATAATACAACAAGACGAGAAGACCCTAAGGA A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs80040932 Functional Loss SNV dbSNP153 33..33 33 - - - 60538 RMVar_ID_60538 Human_SNP_ID_620312723 m1A Human chr17 + 22524131 22524131 22524131 CCAGTGAAATTGACCTGCCCGTGAAGAGGCGGACATAATACAACAAGACGAGAAGACCCTAAGGA CCAGTGAAATTGACCTGCCCGTGAAGAGGCGGGCATAATACAACAAGACGAGAAGACCCTAAGGA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs80040932 Functional Loss SNV dbSNP153 33..33 33 - - - 60539 RMVar_ID_60539 Human_SNP_ID_620873902 m1A Human chr17 - 27353765 27353765 27353765 GGACCGTGGGGCGGCCGGGAGCGAGTGTGGAGACGCGGCCACAGGAACCCAGGACAATGGCGGGA GGACCGTGGGGCGGCCGGGAGCGAGTGTGGAGGCGCGGCCACAGGAACCCAGGACAATGGCGGGA T C lnc-NOS2-11 RNACentral:URS00008B7F23 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:27353655..27353776 26863196 MeRIP-seq:(Medium) rs1442760617 Functional Loss SNV dbSNP153 33..33 33 - - - 60540 RMVar_ID_60540 Human_SNP_ID_620902272 m1A Human chr17 + 27471515 27471515 27471515 CTGGCTTGTGCAAGAGCCCTGAGGCAGAATCGAGCTTGGTGTGGTCAAGGGCCAGGAGGAGGCTG CTGGCTTGTGCAAGAGCCCTGAGGCAGAATCGTGCTTGGTGTGGTCAAGGGCCAGGAGGAGGCTG A T KSR1 Ensembl:ENSG00000141068 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:27471501..27471572 26863196 MeRIP-seq:(Medium) rs976165578 Functional Loss SNV dbSNP153 33..33 33 - - - 60541 RMVar_ID_60541 Human_SNP_ID_620907582 m1A Human chr17 - 27494989 27494989 27494989 GCTGTGCCCACCTGGAACCCGCACTGCCCGGGAGCCCCTTCCCTCTGCCTCTCCAGTCACTGAAT GCTGTGCCCACCTGGAACCCGCACTGCCCGGGTGCCCCTTCCCTCTGCCTCTCCAGTCACTGAAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:27494978..27495054 26863196 MeRIP-seq:(Medium) rs1354341984 Functional Loss SNV dbSNP153 33..33 33 - - - 60542 RMVar_ID_60542 Human_SNP_ID_620914287 m1A Human chr17 + 27524244 27524244 27524244 TGGGCATGTCTGGGAGGAGAGACCACTTGGCCAGATGCCCCAGTGAGGTCAAGCAGGATGAGGGT TGGGCATGTCTGGGAGGAGAGACCACTTGGCCGGATGCCCCAGTGAGGTCAAGCAGGATGAGGGT A G KSR1 Ensembl:ENSG00000141068 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:27524236..27524354 26863196 MeRIP-seq:(Medium) rs1275228665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40409,RMVar_hsa_circ_287307,RMVar_hsa_circ_182790 60543 RMVar_ID_60543 Human_SNP_ID_620916832 m1A Human chr17 + 27534584 27534584 27534584 TTTGAACCCGGGTCTGTTGGCCTCTAGGCCCCAGCACCTGACTATCCATCACTATACTGCCCCTG TTTGAACCCGGGTCTGTTGGCCTCTAGGCCCCGGCACCTGACTATCCATCACTATACTGCCCCTG A G KSR1 Ensembl:ENSG00000141068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:27534563..27534715 26863196 MeRIP-seq:(Medium) rs905181208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40409,RMVar_hsa_circ_287307,RMVar_hsa_circ_182790 60544 RMVar_ID_60544 Human_SNP_ID_620920594 m1A Human chr17 - 27550737 27550737 27550737 TGTGTGTTCCCTCTGCTTGGCCCCTCATGCCTATCCCTATGCTGAGAACCAGCTTGCATACCTGC TGTGTGTTCCCTCTGCTTGGCCCCTCATGCCTGTCCCTATGCTGAGAACCAGCTTGCATACCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:27550732..27550808 26863196 MeRIP-seq:(Medium) rs775750952 Functional Loss SNV dbSNP153 33..33 33 - - - 60545 RMVar_ID_60545 Human_SNP_ID_621006898 m1A Human chr17 + 27889145 27889145 27889145 CTCTTAAACCTGCTGTCCCATGGGAAAACAACAGTTTGGCCATGCTCTGACCAACTCCACAGGCA CTCTTAAACCTGCTGTCCCATGGGAAAACAACTGTTTGGCCATGCTCTGACCAACTCCACAGGCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:27889016..27889158 26863196 MeRIP-seq:(Medium) rs1265664944 Functional Loss SNV dbSNP153 33..33 33 - - - 60546 RMVar_ID_60546 Human_SNP_ID_621043997 m1A Human chr17 + 28041826 28041809 28041827 GGCGGAACCGGCGGCTGAGGAGGCGGCGGCTGAGGAGAAGGCGGCCGCGGCGGCTGAGGAGAAAG GGCGGAACCGGCGGCT__________________GAGAAGGCGGCCGCGGCGGCTGAGGAGAAAG TGAGGAGGCGGCGGCTGAG T NLK Ensembl:ENSG00000087095 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:28041776..28042126 26863196 MeRIP-seq:(Medium) rs1297699088 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_4466185 60547 RMVar_ID_60547 Human_SNP_ID_621044001 m1A Human chr17 + 28041814 28041814 28041814 GAGTCCGGCCGCGGCGGAACCGGCGGCTGAGGAGGCGGCGGCTGAGGAGAAGGCGGCCGCGGCGG GAGTCCGGCCGCGGCGGAACCGGCGGCTGAGGTGGCGGCGGCTGAGGAGAAGGCGGCCGCGGCGG A T NLK Ensembl:ENSG00000087095 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28041765..28041920 26863196 MeRIP-seq:(Medium) rs538066775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466185,Human_RBP_ID_18420572 60548 RMVar_ID_60548 Human_SNP_ID_621044025 m1A Human chr17 + 28041850 28041848 28041851 GGCGGCTGAGGAGAAGGCGGCCGCGGCGGCTGAGGAGAAAGCGGCCGCGGGGACGGAAGCCGGGT GGCGGCTGAGGAGAAGGCGGCCGCGGCGGCT___GAGAAAGCGGCCGCGGGGACGGAAGCCGGGT TGAG T NLK Ensembl:ENSG00000087095 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28041801..28041875 26863196 MeRIP-seq:(Medium) rs1447638312 Functional Loss DEL dbSNP153 32..34 33 - - - 60549 RMVar_ID_60549 Human_SNP_ID_621044026 m1A Human chr17 + 28041850 28041849 28041850 GGCGGCTGAGGAGAAGGCGGCCGCGGCGGCTGAGGAGAAAGCGGCCGCGGGGACGGAAGCCGGGT GGCGGCTGAGGAGAAGGCGGCCGCGGCGGCTG_GGAGAAAGCGGCCGCGGGGACGGAAGCCGGGT GA G NLK Ensembl:ENSG00000087095 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28041801..28041875 26863196 MeRIP-seq:(Medium) rs1407263214 Functional Loss DEL dbSNP153 33..33 33 - - - 60550 RMVar_ID_60550 Human_SNP_ID_621044124 m1A Human chr17 + 28042114 28042114 28042114 GTTCCCTCCGTCTGGGCGTCCGAGCGCTGCCCACATCTTTCATTCCTCCCTGCACCTCCTTCCCT GTTCCCTCCGTCTGGGCGTCCGAGCGCTGCCCCCATCTTTCATTCCTCCCTGCACCTCCTTCCCT A C NLK Ensembl:ENSG00000087095 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28041951..28042250 26863196 MeRIP-seq:(Medium) rs1318519047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1285136,Human_RBP_ID_1367491,Human_RBP_ID_5419931,Human_RBP_ID_5441234,Human_RBP_ID_5466247,Human_RBP_ID_5496722,Human_RBP_ID_12935597,Human_RBP_ID_17003600,Human_RBP_ID_17887634,Human_RBP_ID_20191936,Human_RBP_ID_22056074,Human_RBP_ID_22803614,Human_RBP_ID_25259256 60551 RMVar_ID_60551 Human_SNP_ID_621044283 m1A Human chr17 - 28042512 28042512 28042512 CAAACCTCCCGACCCCCTGAACTCCACACACGAAAAGGATCAGGTAACACACCACCCTTGGAATC CAAACCTCCCGACCCCCTGAACTCCACACACGGAAAGGATCAGGTAACACACCACCCTTGGAATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28042462..28042547 26863196 MeRIP-seq:(Medium) rs1423654761 Functional Loss SNV dbSNP153 33..33 33 - - - 60552 RMVar_ID_60552 Human_SNP_ID_621107236 m1A Human chr17 - 28318421 28318421 28318421 GAGGCAGCTGGCCGCGGTGAACAAAGAAGCAGAGGGGAGGACTCGAGGGACGTAGGAGGCAGTAA GAGGCAGCTGGCCGCGGTGAACAAAGAAGCAGTGGGGAGGACTCGAGGGACGTAGGAGGCAGTAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28318370..28318473 26863196 MeRIP-seq:(Medium) rs1272031649 Functional Loss SNV dbSNP153 33..33 33 - - - 60553 RMVar_ID_60553 Human_SNP_ID_621107581 m1A Human chr17 + 28319364 28319363 28319364 GGCGGTGCTGCCGCGCGAGCTCTACCCAGTCGAGGTGAGGGGCGCCCCTCTTATCCCGGCCCGCT GGCGGTGCTGCCGCGCGAGCTCTACCCAGTCG_GGTGAGGGGCGCCCCTCTTATCCCGGCCCGCT GA G TMEM97 Ensembl:ENSG00000109084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28319326..28319375 32194978 MeRIP-seq:(Medium) rs1197906382 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4464391,Human_RBP_ID_19078581 Human_Splice_Rec_1794913,Human_Splice_Rec_1794917,Human_Splice_Rec_1794921,Human_Splice_Rec_1794923 60554 RMVar_ID_60554 Human_SNP_ID_621109008 m1A Human chr17 + 28325553 28325553 28325553 TGGTATGCTAAGGAGTTCAAAGACCCACTGCTACAGGAGCCCCCAGCCTGGTTTAAGTCCTTTCT TGGTATGCTAAGGAGTTCAAAGACCCACTGCTGCAGGAGCCCCCAGCCTGGTTTAAGTCCTTTCT A G TMEM97 Ensembl:ENSG00000109084 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28325476..28325571 26863196 MeRIP-seq:(Medium) rs782665607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485581,Human_RBP_ID_4465221,Human_RBP_ID_5144076,Human_RBP_ID_6572572,Human_RBP_ID_22761383 Human_Splice_Rec_1794914,Human_Splice_Rec_1794915,Human_Splice_Rec_1794918,Human_Splice_Rec_1794919,Human_Splice_Rec_1794922,Human_Splice_Rec_1794928,Human_Splice_Rec_1794929 60555 RMVar_ID_60555 Human_SNP_ID_621111647 m1A Human chr17 + 28335424 28335424 28335424 AGCTTCTCCTGGGTCAGCGACAGCCGGTACCCAGCCAGCCTGCCACGGCCGCTGCCACGGATACA AGCTTCTCCTGGGTCAGCGACAGCCGGTACCCGGCCAGCCTGCCACGGCCGCTGCCACGGATACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28335347..28335445 26863196 MeRIP-seq:(Medium) rs1484261457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100403,RMVar_hsa_circ_182825 60556 RMVar_ID_60556 Human_SNP_ID_621111769 m1A Human chr17 + 28335812 28335812 28335812 GGGCAGGCGGCTGCAGGCTAGGGGCGGCTCGGAGTCCGCTGGCCACCCAGCTGAGAGGAGAGGCG GGGCAGGCGGCTGCAGGCTAGGGGCGGCTCGGCGTCCGCTGGCCACCCAGCTGAGAGGAGAGGCG A C TNFAIP1 Ensembl:ENSG00000109079 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28335764..28335912 26863196 MeRIP-seq:(Medium) rs1289042046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822037,Human_RBP_ID_4413015,Human_RBP_ID_18419915,Human_RBP_ID_19081833,Human_RBP_ID_22498990 Human_Splice_Rec_1795033,Human_Splice_Rec_1795047,Human_Splice_Rec_1795055 RMVar_hsa_circ_100403,RMVar_hsa_circ_182825 60557 RMVar_ID_60557 Human_SNP_ID_621114322 m1A Human chr17 + 28345555 28345555 28345555 CCTCACATACGGTAAAGCCAAAGAGCTGTCACATGGGCCAGAAACATGAGCCACGGCAGGAAGAC CCTCACATACGGTAAAGCCAAAGAGCTGTCACGTGGGCCAGAAACATGAGCCACGGCAGGAAGAC A G TNFAIP1 Ensembl:ENSG00000109079 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28345506..28345607 26863196 MeRIP-seq:(Medium) rs1354894846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_133270,Human_RBP_ID_12938191 60558 RMVar_ID_60558 Human_SNP_ID_621114945 m1A Human chr17 - 28348100 28348100 28348100 AGGCCTTCACTGGTAGGCCAGCTGAGGCCCCAAGTGCCCAGGCTTGGTCACCGGGAAGAACAACT AGGCCTTCACTGGTAGGCCAGCTGAGGCCCCAGGTGCCCAGGCTTGGTCACCGGGAAGAACAACT T C POLDIP2 Ensembl:ENSG00000004142 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1555579301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4469622,Human_RBP_ID_8447525,Human_RBP_ID_18988070,Human_RBP_ID_26812029 RMVar_hsa_circ_182830,RMVar_hsa_circ_78028,RMVar_hsa_circ_108043,RMVar_hsa_circ_182831 60559 RMVar_ID_60559 Human_SNP_ID_621115200 m1A Human chr17 + 28349084 28349084 28349084 GTGGCCCCTACTGCTGTGCACACTCACTCACCACATGTGCCCACTGGAAGCCTGCAGCGAGACGT GTGGCCCCTACTGCTGTGCACACTCACTCACCCCATGTGCCCACTGGAAGCCTGCAGCGAGACGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:28349076..28349175;chr17:28349076..28349100 32194978 MeRIP-seq:(Medium) rs1481824877 Functional Loss SNV dbSNP153 33..33 33 - - - 60560 RMVar_ID_60560 Human_SNP_ID_621115201 m1A Human chr17 + 28349084 28349084 28349084 GTGGCCCCTACTGCTGTGCACACTCACTCACCACATGTGCCCACTGGAAGCCTGCAGCGAGACGT GTGGCCCCTACTGCTGTGCACACTCACTCACCGCATGTGCCCACTGGAAGCCTGCAGCGAGACGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:28349076..28349175;chr17:28349076..28349100 32194978 MeRIP-seq:(Medium) rs1481824877 Functional Loss SNV dbSNP153 33..33 33 - - - 60561 RMVar_ID_60561 Human_SNP_ID_621115569 m1A Human chr17 + 28350545 28350545 28350545 GAGCTGTACCACATCACTGTCAAGGTTCTCCAAACGGATACAGTAGCGCCACTGAGGTGGGTGTG GAGCTGTACCACATCACTGTCAAGGTTCTCCAGACGGATACAGTAGCGCCACTGAGGTGGGTGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28350403..28350573 26863196 MeRIP-seq:(Medium) rs1202867674 Functional Loss SNV dbSNP153 33..33 33 - - - 60562 RMVar_ID_60562 Human_SNP_ID_621117418 m1A Human chr17 - 28357280 28357279 28357280 CGACGCGGAGGCACCTCTCGTCCCGGTGAGGGACGGAGCCAGGGGGCGCGAGGAACTGGGCCTGG CGACGCGGAGGCACCTCTCGTCCCGGTGAGGG_CGGAGCCAGGGGGCGCGAGGAACTGGGCCTGG GT G POLDIP2 Ensembl:ENSG00000004142 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28357276..28357300 26863196 MeRIP-seq:(Medium) rs552965062 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_237432,Human_RBP_ID_8941809,Human_RBP_ID_19078589 60563 RMVar_ID_60563 Human_SNP_ID_621117419 m1A Human chr17 - 28357280 28357280 28357280 CGACGCGGAGGCACCTCTCGTCCCGGTGAGGGACGGAGCCAGGGGGCGCGAGGAACTGGGCCTGG CGACGCGGAGGCACCTCTCGTCCCGGTGAGGGGCGGAGCCAGGGGGCGCGAGGAACTGGGCCTGG T C POLDIP2 Ensembl:ENSG00000004142 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28357276..28357300 26863196 MeRIP-seq:(Medium) rs370809049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237432,Human_RBP_ID_8941809,Human_RBP_ID_19078589 60564 RMVar_ID_60564 Human_SNP_ID_621117525 m1A Human chr17 - 28357443 28357443 28357443 GCAGCCGGGCGGGCGCTCGGGCGGGACATGGCAGCCTGTACAGCCCGGCGGGCCCTGGCCGTGGG GCAGCCGGGCGGGCGCTCGGGCGGGACATGGCGGCCTGTACAGCCCGGCGGGCCCTGGCCGTGGG T C POLDIP2 Ensembl:ENSG00000004142 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28357325..28357575 26863196 MeRIP-seq:(Medium) rs1555581234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767862,Human_RBP_ID_4464392,Human_RBP_ID_5318308,Human_RBP_ID_18419563 60565 RMVar_ID_60565 Human_SNP_ID_621117728 m1A Human chr17 - 28357712 28357712 28357712 CGCTCTGGCTCCAGCTCCCCGCCGGGGCCCAAAGCACGCACCAATCGCTCGCCCGCAAGCAAAGA CGCTCTGGCTCCAGCTCCCCGCCGGGGCCCAAGGCACGCACCAATCGCTCGCCCGCAAGCAAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:28357651..28358931;chr17:28357651..28358981 26863196 MeRIP-seq:(Medium) rs782278381 Functional Loss SNV dbSNP153 33..33 33 - - - 60566 RMVar_ID_60566 Human_SNP_ID_621117737 m1A Human chr17 + 28357729 28357729 28357729 GCGATTGGTGCGTGCTTTGGGCCCCGGCGGGGAGCTGGAGCCAGAGCGGCTACCCCGAAAGCTGC GCGATTGGTGCGTGCTTTGGGCCCCGGCGGGGTGCTGGAGCCAGAGCGGCTACCCCGAAAGCTGC A T AC002094.1,TMEM199 Ensembl:ENSG00000258924,Ensembl:ENSG00000244045 lincRNA,Protein coding exon,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:28357679..28357806 26863196 MeRIP-seq:(Medium) rs1555581397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766943,Human_RBP_ID_820114,Human_RBP_ID_901458,Human_RBP_ID_4465228,Human_RBP_ID_5649211,Human_RBP_ID_17887785,Human_RBP_ID_18419564,Human_RBP_ID_18988072,Human_RBP_ID_22443511 60567 RMVar_ID_60567 Human_SNP_ID_621117745 m1A Human chr17 - 28357747 28357747 28357747 CGGCCTCAAGCTCGGCCCGCAGCTTTCGGGGTAGCCGCTCTGGCTCCAGCTCCCCGCCGGGGCCC CGGCCTCAAGCTCGGCCCGCAGCTTTCGGGGTCGCCGCTCTGGCTCCAGCTCCCCGCCGGGGCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28357696..28357812 26863196 MeRIP-seq:(Medium) rs782558096 Functional Loss SNV dbSNP153 33..33 33 - - - 60568 RMVar_ID_60568 Human_SNP_ID_621122131 m1A Human chr17 + 28371775 28371775 28371775 GCCGCCTCCTCTACCCTACGGCGTCCGGAGCCATCCCTCGCCTGCTCGCTCTCTCCTTTCGCCCA GCCGCCTCCTCTACCCTACGGCGTCCGGAGCCGTCCCTCGCCTGCTCGCTCTCTCCTTTCGCCCA A G AC002094.1,SARM1 Ensembl:ENSG00000258924,Ensembl:ENSG00000004139 lincRNA,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:28371676..28371875 26863410 MeRIP-seq:(Medium) rs954227785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4413231,Human_RBP_ID_5291395 60569 RMVar_ID_60569 Human_SNP_ID_621125893 m1A Human chr17 + 28385640 28385640 28385640 CTGACCATGTCTTGAGAGGTGCACTGGCGGGGAGGGGTGGCAACAGGAAGGGCAGCCCAGGCAGA CTGACCATGTCTTGAGAGGTGCACTGGCGGGGGGGGGTGGCAACAGGAAGGGCAGCCCAGGCAGA A G SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28385591..28385682 26863196 MeRIP-seq:(Medium) rs1555585940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235469 RMVar_hsa_circ_80080,RMVar_hsa_circ_327482,RMVar_hsa_circ_377723,RMVar_hsa_circ_182841 60570 RMVar_ID_60570 Human_SNP_ID_621128565 m1A Human chr17 + 28396637 28396636 28396637 ATTCCCTTCTCCTGCTGATAGCAGTCAGCTTGAGGAGGATGACGGAAGGCAGCCTCAGACAGGAA ATTCCCTTCTCCTGCTGATAGCAGTCAGCTTG_GGAGGATGACGGAAGGCAGCCTCAGACAGGAA GA G SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28396507..28396658 32194978 MeRIP-seq:(Medium) rs1395027956 Functional Loss DEL dbSNP153 33..33 33 - - - 60571 RMVar_ID_60571 Human_SNP_ID_621130825 m1A Human chr17 - 28406116 28406116 28406116 CGCCCGCCTGGCGACAGCTCCGCCGCGCACGCACATGGAGGGGAGCGCGAGCCCCCCGGAAAAGC CGCCCGCCTGGCGACAGCTCCGCCGCGCACGCTCATGGAGGGGAGCGCGAGCCCCCCGGAAAAGC T A SLC46A1 Ensembl:ENSG00000076351 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28406066..28406144 26863196 MeRIP-seq:(Medium) rs1036638980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466204,Human_RBP_ID_22443532 60572 RMVar_ID_60572 Human_SNP_ID_621146226 m1A Human chr17 + 28468133 28468132 28468133 TTTATCGCTCAGAGGAGAATTCTGCCTAAGCCAACTCGAAAAAGCCGTACAAAAAATAAGCAAAA TTTATCGCTCAGAGGAGAATTCTGCCTAAGCC_ACTCGAAAAAGCCGTACAAAAAATAAGCAAAA CA C RPS7P1 Ensembl:ENSG00000263266 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1397151581 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1064002,Human_RBP_ID_3548717,Human_RBP_ID_5098593,Human_RBP_ID_9077484,Human_RBP_ID_26812031 60573 RMVar_ID_60573 Human_SNP_ID_621146258 m1A Human chr17 - 28468210 28468210 28468210 CCACAATTTCGCTTGGGAAGACCAAGTCCTCGAGGATGGCATCGTGCACAGCTGTCAGAGTACGG CCACAATTTCGCTTGGGAAGACCAAGTCCTCGCGGATGGCATCGTGCACAGCTGTCAGAGTACGG T G AC005726.1 Ensembl:ENSG00000258472 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28468191..28468322 26863196 MeRIP-seq:(Medium) rs1242428544 Functional Loss SNV dbSNP153 33..33 33 - - - 60574 RMVar_ID_60574 Human_SNP_ID_621166921 m1A Human chr17 + 28547282 28547282 28547282 CTCCCAGCCCAGAACTGGAGCCTCCTGGGGTCAGGGCAGCCGTGGGGTCAGGGTGTCCCGCTGTA CTCCCAGCCCAGAACTGGAGCCTCCTGGGGTCGGGGCAGCCGTGGGGTCAGGGTGTCCCGCTGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28547232..28547351 26863196 MeRIP-seq:(Medium) rs1334569497 Functional Loss SNV dbSNP153 33..33 33 - - - 60575 RMVar_ID_60575 Human_SNP_ID_621168292 m1A Human chr17 - 28552389 28552389 28552389 GCCCAGGGCCCAGGCCGGGGCCGCTGCAGAGGAAGCAGCCGATCGGGCCGGAGGACGTGCTGGGG GCCCAGGGCCCAGGCCGGGGCCGCTGCAGAGGTAGCAGCCGATCGGGCCGGAGGACGTGCTGGGG T A AC005726.1,UNC119 Ensembl:ENSG00000258472,Ensembl:ENSG00000109103 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28552303..28552581 26863196 MeRIP-seq:(Medium) rs267607166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4413530,Human_RBP_ID_22959785 Human_Splice_Rec_1795541,Human_Splice_Rec_1795549,Human_Splice_Rec_1795559,Human_Splice_Rec_1795561,Human_Splice_Rec_1795571 Clinvar_Rec_213 RMVar_hsa_circ_182845,RMVar_hsa_circ_99874 60576 RMVar_ID_60576 Human_SNP_ID_621168333 m1A Human chr17 + 28552484 28552484 28552484 CGGATTCCGCAGGCGGCTGTGGTATGGGGGCCACGCTCTGGCCCGAGGGCCCCGGAGCGGACTCC CGGATTCCGCAGGCGGCTGTGGTATGGGGGCCCCGCTCTGGCCCGAGGGCCCCGGAGCGGACTCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28552074..28552550 32194978 MeRIP-seq:(Medium) rs1484063034 Functional Loss SNV dbSNP153 33..33 33 - - - 60577 RMVar_ID_60577 Human_SNP_ID_621171196 m1A Human chr17 - 28563522 28563522 28563522 GCTCTTGGTGTACCACCTGTTCTTGCCCCCAGAGGCAGAAGCCATGTTAGATGAGCCTCAGGAAC GCTCTTGGTGTACCACCTGTTCTTGCCCCCAGGGGCAGAAGCCATGTTAGATGAGCCTCAGGAAC T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:28563501..28563525;chr17:28561782..28563565 26863196,32194978 MeRIP-seq:(Medium) rs1307204314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17904728,Human_RBP_ID_22761423,Human_RBP_ID_27838736 Human_Splice_Rec_1795578,Human_Splice_Rec_1795579,Human_Splice_Rec_1795606,Human_Splice_Rec_1795607,Human_Splice_Rec_1795626,Human_Splice_Rec_1795627,Human_Splice_Rec_1795645,Human_Splice_Rec_1795658,Human_Splice_Rec_1795659,Human_Splice_Rec_1795666,Human_Splice_Rec_1795667,Human_Splice_Rec_1795676,Human_Splice_Rec_1795677,Human_Splice_Rec_1795686 RMVar_hsa_circ_8487,RMVar_hsa_circ_97593,RMVar_hsa_circ_88032,RMVar_hsa_circ_93733,RMVar_hsa_circ_182847,RMVar_hsa_circ_182849,RMVar_hsa_circ_182848,RMVar_hsa_circ_182851,RMVar_hsa_circ_372160 60578 RMVar_ID_60578 Human_SNP_ID_621173004 m1A Human chr17 - 28571472 28571472 28571472 AAGCTAGCATGGCGGCCGCCGGGGCTGCGGCTACACACCTAGGTGCGGTGGGCTTCGGGTGGGGG AAGCTAGCATGGCGGCCGCCGGGGCTGCGGCTGCACACCTAGGTGCGGTGGGCTTCGGGTGGGGG T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28571378..28571498 26863196 MeRIP-seq:(Medium) rs770272089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820031,Human_RBP_ID_4464405,Human_RBP_ID_6573048,Human_RBP_ID_18420574,Human_RBP_ID_23717802 Human_Splice_Rec_1795573,Human_Splice_Rec_1795599,Human_Splice_Rec_1795671,Human_Splice_Rec_1795681,Human_Splice_Rec_1795687 RMVar_hsa_circ_88032,RMVar_hsa_circ_182849 60579 RMVar_ID_60579 Human_SNP_ID_621176463 m1A Human chr17 + 28584703 28584703 28584703 TTCCAACTCCAGTTGTTCTGTTTGGCCTTTGCACTCCTCTAACTGGGCAGAGACTTGTTCCAGCA TTCCAACTCCAGTTGTTCTGTTTGGCCTTTGCGCTCCTCTAACTGGGCAGAGACTTGTTCCAGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28584651..28584750 32194978 MeRIP-seq:(Medium) rs767597745 Functional Loss SNV dbSNP153 33..33 33 - - - 60580 RMVar_ID_60580 Human_SNP_ID_621179886 m1A Human chr17 - 28598627 28598627 28598627 CCTCTTTCTTGGTTTCTTTCTCAGGGAAAACCATCTATGAGAACTCCTCTCCGTGAACTTACCCT CCTCTTTCTTGGTTTCTTTCTCAGGGAAAACCGTCTATGAGAACTCCTCTCCGTGAACTTACCCT T C AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28598576..28598650 26863196 MeRIP-seq:(Medium) rs775109728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066813,Human_RBP_ID_3951986,Human_RBP_ID_9288834,Human_RBP_ID_9375527 Human_Splice_Rec_1795804,Human_Splice_Rec_1795934,Human_Splice_Rec_1795940,Human_Splice_Rec_1795946 Human_miRNA_ID_846457 RMVar_hsa_circ_182875 60581 RMVar_ID_60581 Human_SNP_ID_621180002 m1A Human chr17 - 28598974 28598974 28598974 GGGTGAACATGGCGTCCTCGACTTGGTCTGAGACGTGATAGGCCTGCCTTCTGGTTGAAGATGTG GGGTGAACATGGCGTCCTCGACTTGGTCTGAGTCGTGATAGGCCTGCCTTCTGGTTGAAGATGTG T A AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28598951..28599025 26863196 MeRIP-seq:(Medium) rs1282564204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768054,Human_RBP_ID_1530109,Human_RBP_ID_1851977,Human_RBP_ID_4413821,Human_RBP_ID_9288836,Human_RBP_ID_18692419,Human_RBP_ID_22445360,Human_RBP_ID_22531545,Human_RBP_ID_23717830 Human_Splice_Rec_1795803,Human_Splice_Rec_1795933,Human_Splice_Rec_1795939,Human_Splice_Rec_1795945 RMVar_hsa_circ_182875 60582 RMVar_ID_60582 Human_SNP_ID_621182171 m1A Human chr17 + 28605301 28605301 28605301 TGAGAGGGAGACCATGGAAAGGAGGGAGAGGGAGAGGGTTCGGCATGAGAGGGAGACCGTGGAAA TGAGAGGGAGACCATGGAAAGGAGGGAGAGGGGGAGGGTTCGGCATGAGAGGGAGACCGTGGAAA A G SPAG5-AS1 Ensembl:ENSG00000227543 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28605253..28605329 26863196 MeRIP-seq:(Medium) rs1351274219 Functional Loss SNV dbSNP153 33..33 33 - - - 60583 RMVar_ID_60583 Human_SNP_ID_621184969 m1A Human chr17 - 28615143 28615141 28615144 GGACCTGAACATGCAACAGCAGGAAGAGGAGGAGAAAGCCCGGCTCCTCATTGGTTTAAGTGTGG GGACCTGAACATGCAACAGCAGGAAGAGGAG___AAAGCCCGGCTCCTCATTGGTTTAAGTGTGG TCTC T KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28615094..28615214 26863196 MeRIP-seq:(Medium) rs753979041 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_767882,Human_RBP_ID_1852031,Human_RBP_ID_5576952,Human_RBP_ID_8824485,Human_RBP_ID_9289881,Human_RBP_ID_18412007,Human_RBP_ID_18692457 60584 RMVar_ID_60584 Human_SNP_ID_621185117 m1A Human chr17 - 28615734 28615734 28615734 TAACCTGGTGCTGCCCTGTCTGGAGTACCACAACAACACATGGACATGGCTAGACTTTGCCATGG TAACCTGGTGCTGCCCTGTCTGGAGTACCACAGCAACACATGGACATGGCTAGACTTTGCCATGG T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28615657..28615733 26863196 MeRIP-seq:(Medium) rs1381450043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46638,Human_RBP_ID_1530133,Human_RBP_ID_1852041,Human_RBP_ID_8814825,Human_RBP_ID_9258178,Human_RBP_ID_9375529,Human_RBP_ID_18411885 Human_Splice_Rec_1796158,Human_Splice_Rec_1796159,Human_Splice_Rec_1796232,Human_Splice_Rec_1796233,Human_Splice_Rec_1796308,Human_Splice_Rec_1796309 RMVar_hsa_circ_93293,RMVar_hsa_circ_30526,RMVar_hsa_circ_182879 60585 RMVar_ID_60585 Human_SNP_ID_621186616 m1A Human chr17 - 28621148 28621148 28621148 CTCTTCCCAGATTGGAACCAGCCAGCTGAGGCACAGCAAGCCCAGCAAGTCCAGCGGATCATTTC CTCTTCCCAGATTGGAACCAGCCAGCTGAGGCGCAGCAAGCCCAGCAAGTCCAGCGGATCATTTC T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28620976..28621175 32194978 MeRIP-seq:(Medium) rs765157879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905204,Human_RBP_ID_1006921,Human_RBP_ID_1530142,Human_RBP_ID_1852075,Human_RBP_ID_8814860,Human_RBP_ID_9258184,Human_RBP_ID_9289892,Human_RBP_ID_18990796,Human_RBP_ID_25336767,Human_RBP_ID_26333025 Human_Splice_Rec_1796140,Human_Splice_Rec_1796214,Human_Splice_Rec_1796288 Human_miRNA_ID_2546168,Human_miRNA_ID_2554829 RMVar_hsa_circ_3779,RMVar_hsa_circ_1620,RMVar_hsa_circ_93293,RMVar_hsa_circ_124962,RMVar_hsa_circ_182879,RMVar_hsa_circ_109175,RMVar_hsa_circ_91820,RMVar_hsa_circ_79309,RMVar_hsa_circ_102871,RMVar_hsa_circ_126193,RMVar_hsa_circ_182880,RMVar_hsa_circ_182881,RMVar_hsa_circ_111459,RMVar_hsa_circ_182882,RMVar_hsa_circ_182883,RMVar_hsa_circ_182884,RMVar_hsa_circ_119013,RMVar_hsa_circ_182887,RMVar_hsa_circ_76751,RMVar_hsa_circ_182886,RMVar_hsa_circ_97094,RMVar_hsa_circ_107928,RMVar_hsa_circ_92306,RMVar_hsa_circ_113252,RMVar_hsa_circ_182891,RMVar_hsa_circ_46095,RMVar_hsa_circ_88727,RMVar_hsa_circ_182893,RMVar_hsa_circ_182894,RMVar_hsa_circ_182892,RMVar_hsa_circ_309955,RMVar_hsa_circ_182889,RMVar_hsa_circ_182890,RMVar_hsa_circ_345047,RMVar_hsa_circ_309752,RMVar_hsa_circ_278938,RMVar_hsa_circ_90520,RMVar_hsa_circ_96387,RMVar_hsa_circ_43653,RMVar_hsa_circ_83753,RMVar_hsa_circ_98153,RMVar_hsa_circ_182895,RMVar_hsa_circ_182896,RMVar_hsa_circ_182897,RMVar_hsa_circ_103969,RMVar_hsa_circ_126412,RMVar_hsa_circ_182899,RMVar_hsa_circ_94576,RMVar_hsa_circ_182900,RMVar_hsa_circ_182898,RMVar_hsa_circ_114976,RMVar_hsa_circ_119340,RMVar_hsa_circ_109695,RMVar_hsa_circ_65302,RMVar_hsa_circ_182902,RMVar_hsa_circ_182904,RMVar_hsa_circ_182905,RMVar_hsa_circ_182903,RMVar_hsa_circ_18410,RMVar_hsa_circ_182901,RMVar_hsa_circ_85766,RMVar_hsa_circ_89486,RMVar_hsa_circ_182906,RMVar_hsa_circ_76336,RMVar_hsa_circ_182908,RMVar_hsa_circ_182909,RMVar_hsa_circ_182907 60586 RMVar_ID_60586 Human_SNP_ID_621189336 m1A Human chr17 - 28631610 28631610 28631610 TTACCCAGATGGTGAGTGACCTAAGTCAGGTGACCGTTCACCTGATGGCCTCACCCACTGAAGAG TTACCCAGATGGTGAGTGACCTAAGTCAGGTGGCCGTTCACCTGATGGCCTCACCCACTGAAGAG T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28631476..28631700 32194978 MeRIP-seq:(Medium) rs1266162284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485869,Human_RBP_ID_1852089,Human_RBP_ID_8814884,Human_RBP_ID_9258189,Human_RBP_ID_9288845,Human_RBP_ID_18190756,Human_RBP_ID_18470010,Human_RBP_ID_18692497,Human_RBP_ID_22760734,Human_RBP_ID_26640669 Human_Splice_Rec_1796130,Human_Splice_Rec_1796204,Human_Splice_Rec_1796278,Human_Splice_Rec_1796332 Human_miRNA_ID_3096577 RMVar_hsa_circ_3779,RMVar_hsa_circ_1620,RMVar_hsa_circ_93293,RMVar_hsa_circ_124962,RMVar_hsa_circ_182879,RMVar_hsa_circ_109175,RMVar_hsa_circ_91820,RMVar_hsa_circ_102871,RMVar_hsa_circ_126193,RMVar_hsa_circ_182880,RMVar_hsa_circ_182881,RMVar_hsa_circ_111459,RMVar_hsa_circ_182882,RMVar_hsa_circ_182883,RMVar_hsa_circ_182884,RMVar_hsa_circ_119013,RMVar_hsa_circ_182887,RMVar_hsa_circ_76751,RMVar_hsa_circ_97094,RMVar_hsa_circ_107928,RMVar_hsa_circ_92306,RMVar_hsa_circ_113252,RMVar_hsa_circ_182891,RMVar_hsa_circ_88727,RMVar_hsa_circ_182893,RMVar_hsa_circ_182894,RMVar_hsa_circ_182892,RMVar_hsa_circ_309955,RMVar_hsa_circ_182889,RMVar_hsa_circ_182890,RMVar_hsa_circ_278938,RMVar_hsa_circ_90520,RMVar_hsa_circ_96387,RMVar_hsa_circ_83753,RMVar_hsa_circ_98153,RMVar_hsa_circ_182895,RMVar_hsa_circ_182896,RMVar_hsa_circ_182897,RMVar_hsa_circ_126412,RMVar_hsa_circ_182899,RMVar_hsa_circ_94576,RMVar_hsa_circ_182898,RMVar_hsa_circ_114976,RMVar_hsa_circ_119340,RMVar_hsa_circ_109695,RMVar_hsa_circ_182902,RMVar_hsa_circ_182904,RMVar_hsa_circ_182905,RMVar_hsa_circ_182903,RMVar_hsa_circ_182901,RMVar_hsa_circ_85766,RMVar_hsa_circ_89486,RMVar_hsa_circ_76336,RMVar_hsa_circ_107847,RMVar_hsa_circ_182908,RMVar_hsa_circ_182909,RMVar_hsa_circ_182907,RMVar_hsa_circ_77620,RMVar_hsa_circ_100007,RMVar_hsa_circ_123459,RMVar_hsa_circ_182910,RMVar_hsa_circ_182911,RMVar_hsa_circ_103027,RMVar_hsa_circ_81329,RMVar_hsa_circ_89427,RMVar_hsa_circ_182912,RMVar_hsa_circ_182914,RMVar_hsa_circ_182915,RMVar_hsa_circ_182913,RMVar_hsa_circ_119185,RMVar_hsa_circ_55998,RMVar_hsa_circ_182916,RMVar_hsa_circ_182918,RMVar_hsa_circ_83485,RMVar_hsa_circ_182917,RMVar_hsa_circ_376356,RMVar_hsa_circ_124990,RMVar_hsa_circ_182919,RMVar_hsa_circ_182920 60587 RMVar_ID_60587 Human_SNP_ID_621189408 m1A Human chr17 + 28631805 28631805 28631805 AAAACAAGGAACAGGATAGGAGAAATGAAAGGAGTCTTTCATTTTACCTTGAGGTATAAGCCGCT AAAACAAGGAACAGGATAGGAGAAATGAAAGGTGTCTTTCATTTTACCTTGAGGTATAAGCCGCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28631801..28631925 32194978 MeRIP-seq:(Medium) rs1218363697 Functional Loss SNV dbSNP153 33..33 33 - - - 60588 RMVar_ID_60588 Human_SNP_ID_621190665 m1A Human chr17 - 28635469 28635469 28635469 GTGTTTCCTGAGACTGTACCATCCCTTGCACTAGAGACTTCAGGAACTACTTCTGAGCTAGAAGG GTGTTTCCTGAGACTGTACCATCCCTTGCACTGGAGACTTCAGGAACTACTTCTGAGCTAGAAGG T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28635420..28635519 26863196 MeRIP-seq:(Medium) rs781737805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1852129,Human_RBP_ID_8814948,Human_RBP_ID_9257780,Human_RBP_ID_12940021,Human_RBP_ID_17489801,Human_RBP_ID_18692536,Human_RBP_ID_22061165,Human_RBP_ID_22211315,Human_RBP_ID_27450359 Human_miRNA_ID_2019982,Human_miRNA_ID_2025077,Human_miRNA_ID_2311693,Human_miRNA_ID_2313711,Human_miRNA_ID_2499807,Human_miRNA_ID_2607589,Human_miRNA_ID_2655498 RMVar_hsa_circ_3779,RMVar_hsa_circ_1620,RMVar_hsa_circ_93293,RMVar_hsa_circ_182879,RMVar_hsa_circ_91820,RMVar_hsa_circ_126193,RMVar_hsa_circ_182882,RMVar_hsa_circ_119013,RMVar_hsa_circ_182887,RMVar_hsa_circ_76751,RMVar_hsa_circ_92306,RMVar_hsa_circ_113252,RMVar_hsa_circ_182891,RMVar_hsa_circ_88727,RMVar_hsa_circ_182893,RMVar_hsa_circ_182894,RMVar_hsa_circ_182892,RMVar_hsa_circ_309955,RMVar_hsa_circ_278938,RMVar_hsa_circ_90520,RMVar_hsa_circ_78425,RMVar_hsa_circ_83753,RMVar_hsa_circ_98153,RMVar_hsa_circ_182896,RMVar_hsa_circ_182897,RMVar_hsa_circ_126412,RMVar_hsa_circ_182898,RMVar_hsa_circ_119340,RMVar_hsa_circ_182904,RMVar_hsa_circ_182905,RMVar_hsa_circ_182903,RMVar_hsa_circ_85766,RMVar_hsa_circ_182909,RMVar_hsa_circ_77620,RMVar_hsa_circ_100007,RMVar_hsa_circ_123459,RMVar_hsa_circ_182911,RMVar_hsa_circ_103027,RMVar_hsa_circ_81329,RMVar_hsa_circ_115135,RMVar_hsa_circ_89427,RMVar_hsa_circ_182912,RMVar_hsa_circ_182914,RMVar_hsa_circ_182915,RMVar_hsa_circ_182913,RMVar_hsa_circ_119185,RMVar_hsa_circ_55998,RMVar_hsa_circ_182918,RMVar_hsa_circ_182917,RMVar_hsa_circ_376356,RMVar_hsa_circ_124990,RMVar_hsa_circ_182919,RMVar_hsa_circ_182920,RMVar_hsa_circ_125782,RMVar_hsa_circ_109875,RMVar_hsa_circ_112452,RMVar_hsa_circ_111069,RMVar_hsa_circ_105811,RMVar_hsa_circ_81303,RMVar_hsa_circ_28661,RMVar_hsa_circ_182921,RMVar_hsa_circ_182925,RMVar_hsa_circ_182927,RMVar_hsa_circ_182928,RMVar_hsa_circ_182926,RMVar_hsa_circ_182923,RMVar_hsa_circ_182924,RMVar_hsa_circ_182922,RMVar_hsa_circ_78433,RMVar_hsa_circ_107180,RMVar_hsa_circ_101316,RMVar_hsa_circ_80554,RMVar_hsa_circ_127134,RMVar_hsa_circ_182935,RMVar_hsa_circ_182936,RMVar_hsa_circ_182934,RMVar_hsa_circ_110553,RMVar_hsa_circ_182937,RMVar_hsa_circ_182938,RMVar_hsa_circ_182939,RMVar_hsa_circ_109963,RMVar_hsa_circ_76912,RMVar_hsa_circ_120619,RMVar_hsa_circ_375774,RMVar_hsa_circ_182940,RMVar_hsa_circ_125879,RMVar_hsa_circ_101966,RMVar_hsa_circ_182941,RMVar_hsa_circ_182943,RMVar_hsa_circ_182944,RMVar_hsa_circ_182945,RMVar_hsa_circ_182942 60589 RMVar_ID_60589 Human_SNP_ID_621193711 m1A Human chr17 + 28645032 28645032 28645032 GAGGGCGCTAAGCGCAACTAGCAGCAAGACCAACAGCGCGGAGAAGAACAGAGGCATTTAGGTCC GAGGGCGCTAAGCGCAACTAGCAGCAAGACCAGCAGCGCGGAGAAGAACAGAGGCATTTAGGTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28644976..28645150 26863196 MeRIP-seq:(Medium) rs142296849 Functional Loss SNV dbSNP153 33..33 33 - - - 60590 RMVar_ID_60590 Human_SNP_ID_621196582 m1A Human chr17 - 28655401 28655401 28655401 AGTTACTGGAGGATACGGGGGAAGAGTGCCACAGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG AGTTACTGGAGGATACGGGGGAAGAGTGCCACTGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG T A SDF2 Ensembl:ENSG00000132581 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28655351..28655517 32194978 MeRIP-seq:(Medium) rs746151655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115097,Human_RBP_ID_17654618,Human_RBP_ID_18692596,Human_RBP_ID_22443545,Human_RBP_ID_22760737 Human_Splice_Rec_1796418,Human_Splice_Rec_1796424,Human_Splice_Rec_1796428,Human_Splice_Rec_1796434,Human_Splice_Rec_1796440,Human_Splice_Rec_1796448 RMVar_hsa_circ_182959,RMVar_hsa_circ_291816,RMVar_hsa_circ_182960,RMVar_hsa_circ_331244 60591 RMVar_ID_60591 Human_SNP_ID_621196583 m1A Human chr17 - 28655401 28655401 28655401 AGTTACTGGAGGATACGGGGGAAGAGTGCCACAGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG AGTTACTGGAGGATACGGGGGAAGAGTGCCACCGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG T G SDF2 Ensembl:ENSG00000132581 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28655351..28655517 32194978 MeRIP-seq:(Medium) rs746151655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115097,Human_RBP_ID_17654618,Human_RBP_ID_18692596,Human_RBP_ID_22443545,Human_RBP_ID_22760737 Human_Splice_Rec_1796418,Human_Splice_Rec_1796424,Human_Splice_Rec_1796428,Human_Splice_Rec_1796434,Human_Splice_Rec_1796440,Human_Splice_Rec_1796448 RMVar_hsa_circ_182959,RMVar_hsa_circ_291816,RMVar_hsa_circ_182960,RMVar_hsa_circ_331244 60592 RMVar_ID_60592 Human_SNP_ID_621198676 m1A Human chr17 + 28661851 28661851 28661851 TGGACGCTCCCACAGCGCTCCACAAACCCCCCAACAACAGCAGAGGTACTACAGCCATCCTAACT TGGACGCTCCCACAGCGCTCCACAAACCCCCCGACAACAGCAGAGGTACTACAGCCATCCTAACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:28661647..28661911;chr17:28661661..28661871 26863196 MeRIP-seq:(Medium) rs1386519247 Functional Loss SNV dbSNP153 33..33 33 - - - 60593 RMVar_ID_60593 Human_SNP_ID_621198808 m1A Human chr17 + 28662128 28662128 28662128 GCTTCGGTTACCTTTCGCACCCACGAGACGAAAGCTTCCGAGAGCGGGAGAGAGAACAAGAAATG GCTTCGGTTACCTTTCGCACCCACGAGACGAACGCTTCCGAGAGCGGGAGAGAGAACAAGAAATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:28661972..28662140;chr17:28661984..28662127 26863196 MeRIP-seq:(Medium) rs924482978 Functional Loss SNV dbSNP153 33..33 33 - - - 60594 RMVar_ID_60594 Human_SNP_ID_621198895 m1A Human chr17 - 28662265 28662265 28662265 GGAAAATGGAGTCGTCGAACCGAGACTGGGAAAAGATAGTACGGACCCACCGCACGGCCCCTCCG GGAAAATGGAGTCGTCGAACCGAGACTGGGAAGAGATAGTACGGACCCACCGCACGGCCCCTCCG T C RF00017-1166,lnc-SDF2-3 RNACentral:URS00009832A9,RNACentral:URS00008B6876 SRP RNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28662214..28670955 26863196 MeRIP-seq:(Medium) rs1302326183 Functional Loss SNV dbSNP153 33..33 33 - - - 60595 RMVar_ID_60595 Human_SNP_ID_621198900 m1A Human chr17 - 28662275 28662275 28662275 CCCCCACCGAGGAAAATGGAGTCGTCGAACCGAGACTGGGAAAAGATAGTACGGACCCACCGCAC CCCCCACCGAGGAAAATGGAGTCGTCGAACCGGGACTGGGAAAAGATAGTACGGACCCACCGCAC T C RF00017-1166,lnc-SDF2-3 RNACentral:URS00009832A9,RNACentral:URS00008B6876 SRP RNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28662226..28662394 26863196 MeRIP-seq:(Medium) rs536910875 Functional Loss SNV dbSNP153 33..33 33 - - - 60596 RMVar_ID_60596 Human_SNP_ID_621198933 m1A Human chr17 + 28662339 28662339 28662339 GCTTAGCGCACTGGAGGAGCGGCGGGCTTCAGACAGGTAAAGTTCCGACTGGAGAGCGTGTTTCT GCTTAGCGCACTGGAGGAGCGGCGGGCTTCAGGCAGGTAAAGTTCCGACTGGAGAGCGTGTTTCT A G SUPT6H Ensembl:ENSG00000109111 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28662289..28670955 32194978 MeRIP-seq:(Medium) rs1451276849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237733,Human_RBP_ID_4465242,Human_RBP_ID_8825364,Human_RBP_ID_18419565,Human_RBP_ID_19078630,Human_RBP_ID_22061167,Human_RBP_ID_22959201,Human_RBP_ID_23118868,Human_RBP_ID_26331426 Human_Splice_Rec_1796455,Human_Splice_Rec_1796527 60597 RMVar_ID_60597 Human_SNP_ID_621201948 m1A Human chr17 - 28673490 28673490 28673490 GGGCCTCCTCACCATCATCCTCCTCTTCCACAAATTTCTTGGTGACTCGGGGTACCACCTCGCCT GGGCCTCCTCACCATCATCCTCCTCTTCCACAGATTTCTTGGTGACTCGGGGTACCACCTCGCCT T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:28673364..28673499 26863196 MeRIP-seq:(Medium) rs1338640639 Functional Loss SNV dbSNP153 33..33 33 - - - 60598 RMVar_ID_60598 Human_SNP_ID_621202159 m1A Human chr17 - 28674418 28674418 28674418 ACTACTCACTGCGTTTTCTCTTCTTGTGGCCAACATCATCTTCTGAATCACCAGAGTCACTGCCC ACTACTCACTGCGTTTTCTCTTCTTGTGGCCAGCATCATCTTCTGAATCACCAGAGTCACTGCCC T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28674227..28674625 26863196 MeRIP-seq:(Medium) rs749041928 Functional Loss SNV dbSNP153 33..33 33 - - - 60599 RMVar_ID_60599 Human_SNP_ID_621202354 m1A Human chr17 + 28675053 28675053 28675053 GAGGAATATGGCAAGGAGGAACATGAAAAAGAAGCTATTGCGGAAGAAATCTTCCAGGATGGGGA GAGGAATATGGCAAGGAGGAACATGAAAAAGAGGCTATTGCGGAAGAAATCTTCCAGGATGGGGA A G SUPT6H Ensembl:ENSG00000109111 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28674951..28675150 26863196 MeRIP-seq:(Medium) rs757574596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47652,Human_RBP_ID_201543,Human_RBP_ID_1546640,Human_RBP_ID_1852231,Human_RBP_ID_4414212,Human_RBP_ID_8232319,Human_RBP_ID_9257783,Human_RBP_ID_9375540,Human_RBP_ID_18438605,Human_RBP_ID_18990814,Human_RBP_ID_22061170,Human_RBP_ID_23758833,Human_RBP_ID_24544821,Human_RBP_ID_26330672,Human_RBP_ID_26957722,Human_RBP_ID_27812423 Human_Splice_Rec_1796464,Human_Splice_Rec_1796534,Human_Splice_Rec_1796606 RMVar_hsa_circ_124875,RMVar_hsa_circ_182961,RMVar_hsa_circ_364734,RMVar_hsa_circ_80314,RMVar_hsa_circ_55765,RMVar_hsa_circ_58430,RMVar_hsa_circ_182962,RMVar_hsa_circ_182963,RMVar_hsa_circ_99461,RMVar_hsa_circ_108970,RMVar_hsa_circ_182964,RMVar_hsa_circ_182965,RMVar_hsa_circ_182966,RMVar_hsa_circ_182967,RMVar_hsa_circ_116205 60600 RMVar_ID_60600 Human_SNP_ID_621202355 m1A Human chr17 - 28675056 28675056 28675056 CCTTCCCCATCCTGGAAGATTTCTTCCGCAATAGCTTCTTTTTCATGTTCCTCCTTGCCATATTC CCTTCCCCATCCTGGAAGATTTCTTCCGCAATGGCTTCTTTTTCATGTTCCTCCTTGCCATATTC T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28674937..28675175 26863196 MeRIP-seq:(Medium) rs1567688239 Functional Loss SNV dbSNP153 33..33 33 - - - 60601 RMVar_ID_60601 Human_SNP_ID_621204631 m1A Human chr17 - 28683017 28683017 28683017 TCTTGGAAGGTTTGCCTCAGCACCTGCCGGACAAGGGGCTCACGGGCAATCTGCAGGGCTACCAT TCTTGGAAGGTTTGCCTCAGCACCTGCCGGACGAGGGGCTCACGGGCAATCTGCAGGGCTACCAT T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28682747..28683083 32194978 MeRIP-seq:(Medium) rs777732217 Functional Loss SNV dbSNP153 33..33 33 - - - 60602 RMVar_ID_60602 Human_SNP_ID_621206394 m1A Human chr17 - 28689450 28689450 28689450 GCTCCTGCAGGATTGGCATCCTCGGCTGATTCATCGTATTCCAGGGCATCCACTGCCATCTTCCT GCTCCTGCAGGATTGGCATCCTCGGCTGATTCGTCGTATTCCAGGGCATCCACTGCCATCTTCCT T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28689426..28689450 32194978 MeRIP-seq:(Medium) rs745475952 Functional Loss SNV dbSNP153 33..33 33 - - - 60603 RMVar_ID_60603 Human_SNP_ID_621209224 m1A Human chr17 + 28700249 28700249 28700249 ATCAATGCTACCCCAGCCAACATCAACCTTGCAGGTGAGGAGCTTGAGCCTGGGACTGGAGGTGG ATCAATGCTACCCCAGCCAACATCAACCTTGCCGGTGAGGAGCTTGAGCCTGGGACTGGAGGTGG A C SUPT6H Ensembl:ENSG00000109111 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28700226..28700250 32194978 MeRIP-seq:(Medium) rs200810227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081937 Human_Splice_Rec_1796520,Human_Splice_Rec_1796521,Human_Splice_Rec_1796590,Human_Splice_Rec_1796591,Human_Splice_Rec_1796628,Human_Splice_Rec_1796629,Human_Splice_Rec_1796633 RMVar_hsa_circ_80314,RMVar_hsa_circ_182966,RMVar_hsa_circ_182967,RMVar_hsa_circ_116205,RMVar_hsa_circ_182971,RMVar_hsa_circ_94802,RMVar_hsa_circ_122076,RMVar_hsa_circ_182972,RMVar_hsa_circ_107026,RMVar_hsa_circ_91023,RMVar_hsa_circ_182982,RMVar_hsa_circ_182983,RMVar_hsa_circ_105625,RMVar_hsa_circ_182985,RMVar_hsa_circ_182990,RMVar_hsa_circ_102564 60604 RMVar_ID_60604 Human_SNP_ID_621209451 m1A Human chr17 + 28701055 28701055 28701055 TCACCACCCCTCAGTACCACCAGCTCCAGGCCAGCACCACCCCACAGTCGGCCCAGGCCCAGCCC TCACCACCCCTCAGTACCACCAGCTCCAGGCCGGCACCACCCCACAGTCGGCCCAGGCCCAGCCC A G SUPT6H Ensembl:ENSG00000109111 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28700950..28701100 26863196 MeRIP-seq:(Medium) rs200389208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821342,Human_RBP_ID_5115099,Human_RBP_ID_17263248,Human_RBP_ID_17378239,Human_RBP_ID_22532889,Human_RBP_ID_26458844 Human_Splice_Rec_1796525,Human_Splice_Rec_1796595,Human_Splice_Rec_1796631 RMVar_hsa_circ_80314,RMVar_hsa_circ_182966,RMVar_hsa_circ_182967,RMVar_hsa_circ_116205,RMVar_hsa_circ_182971,RMVar_hsa_circ_94802,RMVar_hsa_circ_122076,RMVar_hsa_circ_182972,RMVar_hsa_circ_107026,RMVar_hsa_circ_182983,RMVar_hsa_circ_182990,RMVar_hsa_circ_102564 60605 RMVar_ID_60605 Human_SNP_ID_621209460 m1A Human chr17 - 28701070 28701070 28701070 GCTGGAAGAGGGCTGGGGCTGGGCCTGGGCCGACTGTGGGGTGGTGCTGGCCTGGAGCTGGTGGT GCTGGAAGAGGGCTGGGGCTGGGCCTGGGCCGGCTGTGGGGTGGTGCTGGCCTGGAGCTGGTGGT T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28701051..28701075 26863196 MeRIP-seq:(Medium) rs1270803653 Functional Loss SNV dbSNP153 33..33 33 - - - 60606 RMVar_ID_60606 Human_SNP_ID_621209587 m1A Human chr17 + 28701469 28701469 28701469 AGGTCCAACAGCCATGCAGCCATCGACTGGGGAAAAATGGCGGAGCAGTGGCTGCAGGAAAAGGA AGGTCCAACAGCCATGCAGCCATCGACTGGGGGAAAATGGCGGAGCAGTGGCTGCAGGAAAAGGA A G SUPT6H Ensembl:ENSG00000109111 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28701432..28701568 26863196 MeRIP-seq:(Medium) rs775873545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1796526,Human_Splice_Rec_1796596,Human_Splice_Rec_1796632 RMVar_hsa_circ_80314,RMVar_hsa_circ_182966,RMVar_hsa_circ_182967,RMVar_hsa_circ_116205,RMVar_hsa_circ_182971,RMVar_hsa_circ_94802,RMVar_hsa_circ_122076,RMVar_hsa_circ_182972,RMVar_hsa_circ_107026,RMVar_hsa_circ_182983,RMVar_hsa_circ_182990,RMVar_hsa_circ_102564 60607 RMVar_ID_60607 Human_SNP_ID_621211632 m1A Human chr17 - 28708383 28708380 28708384 GGAAGAACTAAAGAGCTGGTTAGAGAAGGAAGAGAAAGATGAGGTCTGCCATGGAAGCCCAAGGA GGAAGAACTAAAGAGCTGGTTAGAGAAGGAA____AAGATGAGGTCTGCCATGGAAGCCCAAGGA TTCTC T PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28708332..28708422 26863196 MeRIP-seq:(Medium) rs370754446 Functional Loss DEL dbSNP153 32..35 33 - - - 60608 RMVar_ID_60608 Human_SNP_ID_621212417 m1A Human chr17 + 28711163 28711163 28711163 GGTGGAACCCTCAGTCTCCTTGGTCCACCCTCAGGGTCGATGGAACCGCCCGCTCCCGCCCCGGC GGTGGAACCCTCAGTCTCCTTGGTCCACCCTCTGGGTCGATGGAACCGCCCGCTCCCGCCCCGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28711113..28711238 26863196 MeRIP-seq:(Medium) rs919790356 Functional Loss SNV dbSNP153 33..33 33 - - - 60609 RMVar_ID_60609 Human_SNP_ID_621212633 m1A Human chr17 + 28711689 28711689 28711689 ACATCGCTCTCCGCCCAGGTCTTCGTCTCTACAGGACTCTTGCGTGAAGTCCAACCCTGAGCCTC ACATCGCTCTCCGCCCAGGTCTTCGTCTCTACCGGACTCTTGCGTGAAGTCCAACCCTGAGCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28711185..28712116 26863196 MeRIP-seq:(Medium) rs1350450838 Functional Loss SNV dbSNP153 33..33 33 - - - 60610 RMVar_ID_60610 Human_SNP_ID_621212634 m1A Human chr17 + 28711689 28711689 28711689 ACATCGCTCTCCGCCCAGGTCTTCGTCTCTACAGGACTCTTGCGTGAAGTCCAACCCTGAGCCTC ACATCGCTCTCCGCCCAGGTCTTCGTCTCTACGGGACTCTTGCGTGAAGTCCAACCCTGAGCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28711185..28712116 26863196 MeRIP-seq:(Medium) rs1350450838 Functional Loss SNV dbSNP153 33..33 33 - - - 60611 RMVar_ID_60611 Human_SNP_ID_621213284 m1A Human chr17 + 28714351 28714351 28714351 AGTGAGAGGCTGGAATCATTAAGCATCCTCAAACACAAAGGGCCCAGCAGGCTGAGCAAAAGAAC AGTGAGAGGCTGGAATCATTAAGCATCCTCAAGCACAAAGGGCCCAGCAGGCTGAGCAAAAGAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28714301..28714500 32194978 MeRIP-seq:(Medium) rs15200 Functional Loss SNV dbSNP153 33..33 33 - - - 60612 RMVar_ID_60612 Human_SNP_ID_621213445 m1A Human chr17 + 28714877 28714874 28714877 ATTGGCCTCAAAGGTCAGTGCTGCCACACGGAAGAAGAATTCTCGGACATTCTCACCTGACACAG ATTGGCCTCAAAGGTCAGTGCTGCCACACG___GAAGAATTCTCGGACATTCTCACCTGACACAG GGAA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28714826..28714925 32194978 MeRIP-seq:(Medium) rs764081799 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_12940862 60613 RMVar_ID_60613 Human_SNP_ID_621214316 m1A Human chr17 - 28717519 28717519 28717519 CCCAATTGGCGGCCGAAGAGTCTCCTCGCCCCAGAGTCATCTTCGGGACGCCCAGGGCCCGGGTG CCCAATTGGCGGCCGAAGAGTCTCCTCGCCCCTGAGTCATCTTCGGGACGCCCAGGGCCCGGGTG T A RAB34 Ensembl:ENSG00000109113 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28717501..28717575 26863196 MeRIP-seq:(Medium) rs1421310689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1796918 RMVar_hsa_circ_119538,RMVar_hsa_circ_183002 60614 RMVar_ID_60614 Human_SNP_ID_621214387 m1A Human chr17 + 28717655 28717655 28717655 ACGATTACGCGGGGCCGGATGGTTCCTACAATAACCCGGGGCCGCGGAGACCCGACGTCATCTCG ACGATTACGCGGGGCCGGATGGTTCCTACAATCACCCGGGGCCGCGGAGACCCGACGTCATCTCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28717618..28717843 26863196 MeRIP-seq:(Medium) rs1349837439 Functional Loss SNV dbSNP153 33..33 33 - - - 60615 RMVar_ID_60615 Human_SNP_ID_621214493 m1A Human chr17 + 28718010 28718010 28718010 TGCCCCGCTCAGGCTCCCTCTTTTGACGCTTCACCGGGCACCAGGACCGCCCCGACCCAGGCTGG TGCCCCGCTCAGGCTCCCTCTTTTGACGCTTCCCCGGGCACCAGGACCGCCCCGACCCAGGCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28718008..28718166 26863196 MeRIP-seq:(Medium) rs1385256274 Functional Loss SNV dbSNP153 33..33 33 - - - 60616 RMVar_ID_60616 Human_SNP_ID_621214499 m1A Human chr17 + 28718036 28718036 28718036 CGCTTCACCGGGCACCAGGACCGCCCCGACCCAGGCTGGAGCCTATCCAGATAGGGACTCCCCAG CGCTTCACCGGGCACCAGGACCGCCCCGACCCCGGCTGGAGCCTATCCAGATAGGGACTCCCCAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28718034..28718146 26863196 MeRIP-seq:(Medium) rs1274335519 Functional Loss SNV dbSNP153 33..33 33 - - - 60617 RMVar_ID_60617 Human_SNP_ID_621214507 m1A Human chr17 + 28718067 28718067 28718067 CAGGCTGGAGCCTATCCAGATAGGGACTCCCCAGGCTGCTCTCCCCTGCACCTCTATACCCGGCT CAGGCTGGAGCCTATCCAGATAGGGACTCCCCTGGCTGCTCTCCCCTGCACCTCTATACCCGGCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28718061..28718147 26863196 MeRIP-seq:(Medium) rs530069354 Functional Loss SNV dbSNP153 33..33 33 - - - 60618 RMVar_ID_60618 Human_SNP_ID_621214629 m1A Human chr17 + 28718368 28718368 28718368 GAAGGGGGTGCCAGGGTTAGAATGAGGTGCCCACCGAGGAGAGAGACGTCTGAAGTCTGGCGTCT GAAGGGGGTGCCAGGGTTAGAATGAGGTGCCCGCCGAGGAGAGAGACGTCTGAAGTCTGGCGTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28718317..28718404 26863196 MeRIP-seq:(Medium) rs1195255384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485929 60619 RMVar_ID_60619 Human_SNP_ID_621215110 m1A Human chr17 + 28720029 28720029 28720029 TTTCACAAGATGGCGCCGAAAGCGAAGAAGGAAGGTGTGTGTTGGTGATGGGGCCGCAGCTGGTT TTTCACAAGATGGCGCCGAAAGCGAAGAAGGAGGGTGTGTGTTGGTGATGGGGCCGCAGCTGGTT A G RPL23A Ensembl:ENSG00000198242 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:28719976..28720106;chr17:28720001..28720075 26863410 MeRIP-seq:(Medium) rs1238974412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766696,Human_RBP_ID_902109,Human_RBP_ID_19081939 Human_Splice_Rec_1797013,Human_Splice_Rec_1797021 RMVar_hsa_circ_112873,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005 60620 RMVar_ID_60620 Human_SNP_ID_621215502 m1A Human chr17 - 28720696 28720696 28720696 TCAGCTTTAGGAGGGGCAGGAGCTGGGAGAAAAGGAAAGAAAACGTGGGTGCGGGATTTAGAAAT TCAGCTTTAGGAGGGGCAGGAGCTGGGAGAAATGGAAAGAAAACGTGGGTGCGGGATTTAGAAAT T A RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:28720692..28720925 26863410 MeRIP-seq:(Medium) rs777225080 Functional Loss SNV dbSNP153 33..33 33 - - - 60621 RMVar_ID_60621 Human_SNP_ID_621217679 m1A Human chr17 - 28726052 28726033 28726053 TGCACCCCGCCCTGCCGCTGCTCCTGGGCGCCACGCTGACCTTCCGGGCGCTCCGGCGCGCGCTC TGCACCCCGCCCTGCCGCTGCTCCTGGGCGC____________________TCCGGCGCGCGCTC AGCGCCCGGAAGGTCAGCGTG A TLCD1 Ensembl:ENSG00000160606 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:28725951..28726162 26863410 MeRIP-seq:(Medium) rs779763392 Functional Loss DEL dbSNP153 32..51 33 - - - 60622 RMVar_ID_60622 Human_SNP_ID_621217695 m1A Human chr17 - 28726052 28726052 28726052 TGCACCCCGCCCTGCCGCTGCTCCTGGGCGCCACGCTGACCTTCCGGGCGCTCCGGCGCGCGCTC TGCACCCCGCCCTGCCGCTGCTCCTGGGCGCCTCGCTGACCTTCCGGGCGCTCCGGCGCGCGCTC T A TLCD1 Ensembl:ENSG00000160606 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:28725951..28726162 26863410 MeRIP-seq:(Medium) rs1488494078 Functional Loss SNV dbSNP153 33..33 33 - - - 60623 RMVar_ID_60623 Human_SNP_ID_621217712 m1A Human chr17 - 28726110 28726110 28726110 AGACCTAGGAGGCGGCCTCGAGGGCGGACGGCAGGGAGGGCCAGCATGCCCCGACTGCTGCACCC AGACCTAGGAGGCGGCCTCGAGGGCGGACGGCCGGGAGGGCCAGCATGCCCCGACTGCTGCACCC T G TLCD1 Ensembl:ENSG00000160606 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:28725901..28726175 26863196 MeRIP-seq:(Medium) rs1380536635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464415 60624 RMVar_ID_60624 Human_SNP_ID_621217730 m1A Human chr17 + 28726158 28726158 28726158 GGCCGCCTCCTAGGTCTGTTCTGGGAACCGGGATCCCTCTCGGGCCAGTCCAGGCCGGCCGCCTC GGCCGCCTCCTAGGTCTGTTCTGGGAACCGGGGTCCCTCTCGGGCCAGTCCAGGCCGGCCGCCTC A G NEK8 Ensembl:ENSG00000160602 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28725926..28733994 26863196 MeRIP-seq:(Medium) rs114349053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1530293 GWAS_ID_7298,GWAS_ID_7299,GWAS_ID_7300,GWAS_ID_7301,GWAS_ID_7302,GWAS_ID_7303,GWAS_ID_7304,GWAS_ID_7305,GWAS_ID_7306,GWAS_ID_7307,GWAS_ID_7308,GWAS_ID_7309,GWAS_ID_7310,GWAS_ID_7311,GWAS_ID_7312,GWAS_ID_7313,GWAS_ID_7314,GWAS_ID_7315,GWAS_ID_7316,GWAS_ID_7317,GWAS_ID_7318,GWAS_ID_7319,GWAS_ID_7320,GWAS_ID_7321,GWAS_ID_7322,GWAS_ID_7323,GWAS_ID_7324,GWAS_ID_7325,GWAS_ID_7326,GWAS_ID_7327,GWAS_ID_7328,GWAS_ID_7329,GWAS_ID_7330,GWAS_ID_7331,GWAS_ID_7332,GWAS_ID_7333,GWAS_ID_7334,GWAS_ID_7335,GWAS_ID_7336,GWAS_ID_7337,GWAS_ID_7338,GWAS_ID_7339,GWAS_ID_7340,GWAS_ID_7341,GWAS_ID_7342,GWAS_ID_7343,GWAS_ID_7344,GWAS_ID_7345,GWAS_ID_7346,GWAS_ID_7347,GWAS_ID_7348,GWAS_ID_7349,GWAS_ID_7350,GWAS_ID_7351,GWAS_ID_7352,GWAS_ID_7353,GWAS_ID_7354,GWAS_ID_7355,GWAS_ID_7356 60625 RMVar_ID_60625 Human_SNP_ID_621217781 m1A Human chr17 - 28726312 28726293 28726312 GAGGGGCGGGGGCAGGCGGACGGGGCGGGGGCAGGCGGGCGGGGCGGGGGCGCGGGCGGCTGGGG GAGGGGCGGGGGCAGGCGGACGGGGCGGGGGC___________________GCGGGCGGCTGGGG CGCCCCCGCCCCGCCCGCCT C TLCD1 Ensembl:ENSG00000160606 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28726276..28726325 26863196 MeRIP-seq:(Medium) rs1201009467 Functional Loss DEL dbSNP153 33..51 33 - - - 60626 RMVar_ID_60626 Human_SNP_ID_621217796 m1A Human chr17 - 28726312 28726311 28726313 GAGGGGCGGGGGCAGGCGGACGGGGCGGGGGCAGGCGGGCGGGGCGGGGGCGCGGGCGGCTGGGG GAGGGGCGGGGGCAGGCGGACGGGGCGGGGG__GGCGGGCGGGGCGGGGGCGCGGGCGGCTGGGG CTG C TLCD1 Ensembl:ENSG00000160606 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28726276..28726325 26863196 MeRIP-seq:(Medium) rs1334381405 Functional Loss DEL dbSNP153 32..33 33 - - - 60627 RMVar_ID_60627 Human_SNP_ID_621217797 m1A Human chr17 - 28726312 28726312 28726312 GAGGGGCGGGGGCAGGCGGACGGGGCGGGGGCAGGCGGGCGGGGCGGGGGCGCGGGCGGCTGGGG GAGGGGCGGGGGCAGGCGGACGGGGCGGGGGCGGGCGGGCGGGGCGGGGGCGCGGGCGGCTGGGG T C TLCD1 Ensembl:ENSG00000160606 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28726276..28726325 26863196 MeRIP-seq:(Medium) rs9910062 Functional Loss SNV dbSNP153 33..33 33 - - - 60628 RMVar_ID_60628 Human_SNP_ID_621223296 m1A Human chr17 - 28744356 28744356 28744356 GTCACGGGGCGCCCCTGAGGTCACAGGGTCGCAGCGCAGACAAAGGCCCGCCTTGCCCCGGGCCC GTCACGGGGCGCCCCTGAGGTCACAGGGTCGCGGCGCAGACAAAGGCCCGCCTTGCCCCGGGCCC T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28744352..28744469 26863196 MeRIP-seq:(Medium) rs949157760 Functional Loss SNV dbSNP153 33..33 33 - - - 60629 RMVar_ID_60629 Human_SNP_ID_621223297 m1A Human chr17 - 28744356 28744356 28744356 GTCACGGGGCGCCCCTGAGGTCACAGGGTCGCAGCGCAGACAAAGGCCCGCCTTGCCCCGGGCCC GTCACGGGGCGCCCCTGAGGTCACAGGGTCGCCGCGCAGACAAAGGCCCGCCTTGCCCCGGGCCC T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28744352..28744469 26863196 MeRIP-seq:(Medium) rs949157760 Functional Loss SNV dbSNP153 33..33 33 - - - 60630 RMVar_ID_60630 Human_SNP_ID_621223436 m1A Human chr17 + 28744891 28744891 28744891 TCTCCCGGGGGCTGGAGTAAGGCGGGTGGTCCATAAGTCATGAAGAAGGGGGTCGCACTCGTGTT TCTCCCGGGGGCTGGAGTAAGGCGGGTGGTCCCTAAGTCATGAAGAAGGGGGTCGCACTCGTGTT A C TRAF4 Ensembl:ENSG00000076604 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28744871..28744943 26863196 MeRIP-seq:(Medium) rs1032942638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768057,Human_RBP_ID_896344,Human_RBP_ID_3541624,Human_RBP_ID_4414614,Human_RBP_ID_5129505,Human_RBP_ID_8091937,Human_RBP_ID_22658576,Human_RBP_ID_22716490,Human_RBP_ID_22740265 Human_Splice_Rec_1797191 60631 RMVar_ID_60631 Human_SNP_ID_621223437 m1A Human chr17 + 28744891 28744891 28744891 TCTCCCGGGGGCTGGAGTAAGGCGGGTGGTCCATAAGTCATGAAGAAGGGGGTCGCACTCGTGTT TCTCCCGGGGGCTGGAGTAAGGCGGGTGGTCCGTAAGTCATGAAGAAGGGGGTCGCACTCGTGTT A G TRAF4 Ensembl:ENSG00000076604 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28744871..28744943 26863196 MeRIP-seq:(Medium) rs1032942638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768057,Human_RBP_ID_896344,Human_RBP_ID_3541624,Human_RBP_ID_4414614,Human_RBP_ID_5129505,Human_RBP_ID_8091937,Human_RBP_ID_22658576,Human_RBP_ID_22716490,Human_RBP_ID_22740265 Human_Splice_Rec_1797191 60632 RMVar_ID_60632 Human_SNP_ID_621223568 m1A Human chr17 + 28745319 28745318 28745320 TCCCCACAGCCTGGGCCGGCTCCTGCCCTCACATATGCTCCGGCACAAGCTGCAGGACTGCCCCC TCCCCACAGCCTGGGCCGGCTCCTGCCCTCAC__ATGCTCCGGCACAAGCTGCAGGACTGCCCCC CAT C TRAF4 Ensembl:ENSG00000076604 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28745271..28745495 26863196 MeRIP-seq:(Medium) rs1316371220 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5129507,Human_RBP_ID_17079518 Human_Splice_Rec_1797192 60633 RMVar_ID_60633 Human_SNP_ID_621223569 m1A Human chr17 + 28745319 28745319 28745319 TCCCCACAGCCTGGGCCGGCTCCTGCCCTCACATATGCTCCGGCACAAGCTGCAGGACTGCCCCC TCCCCACAGCCTGGGCCGGCTCCTGCCCTCACTTATGCTCCGGCACAAGCTGCAGGACTGCCCCC A T TRAF4 Ensembl:ENSG00000076604 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28745271..28745495 26863196 MeRIP-seq:(Medium) rs1260268283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129507,Human_RBP_ID_17079518 Human_Splice_Rec_1797192 60634 RMVar_ID_60634 Human_SNP_ID_621223582 m1A Human chr17 - 28745365 28745365 28745365 GGGGCTGTGTCTGTAGGAGAGTAAATGTGTACACTGCCGAGGGGGAGGGGGCAGTCCTGCAGCTT GGGGCTGTGTCTGTAGGAGAGTAAATGTGTACCCTGCCGAGGGGGAGGGGGCAGTCCTGCAGCTT T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28745361..28745635 26863196 MeRIP-seq:(Medium) rs943428652 Functional Loss SNV dbSNP153 33..33 33 - - - 60635 RMVar_ID_60635 Human_SNP_ID_621224393 m1A Human chr17 + 28748102 28748102 28748102 CATGAAGCTGAGCCGCCGTGATCTACCTGCACACTTGCAGCATGACTGCCCCAAGCGGCGCCTCA CATGAAGCTGAGCCGCCGTGATCTACCTGCACGCTTGCAGCATGACTGCCCCAAGCGGCGCCTCA A G TRAF4 Ensembl:ENSG00000076604 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28748052..28748125 26863196 MeRIP-seq:(Medium) rs1226868584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896347,Human_RBP_ID_4414628,Human_RBP_ID_22499047,Human_RBP_ID_23114374,Human_RBP_ID_26812064 Human_Splice_Rec_1797182,Human_Splice_Rec_1797183,Human_Splice_Rec_1797197,Human_Splice_Rec_1797206,Human_Splice_Rec_1797207,Human_Splice_Rec_1797214,Human_Splice_Rec_1797215,Human_Splice_Rec_1797224,Human_Splice_Rec_1797225,Human_Splice_Rec_1797240,Human_Splice_Rec_1797241,Human_Splice_Rec_1797248,Human_Splice_Rec_1797249,Human_Splice_Rec_1797254,Human_Splice_Rec_1797255,Human_Splice_Rec_1797262,Human_Splice_Rec_1797263,Human_Splice_Rec_1797268,Human_Splice_Rec_1797269,Human_Splice_Rec_1797278,Human_Splice_Rec_1797279,Human_Splice_Rec_1797285 RMVar_hsa_circ_105409,RMVar_hsa_circ_183019,RMVar_hsa_circ_183016,RMVar_hsa_circ_91865,RMVar_hsa_circ_281574,RMVar_hsa_circ_183018 60636 RMVar_ID_60636 Human_SNP_ID_621224934 m1A Human chr17 + 28749736 28749736 28749736 CCTCCCCCAGCCACCACCCTCAGGTGCCTCCAATTGGTGCTTCAGCCCTGGCCCCTGTGGGGAAC CCTCCCCCAGCCACCACCCTCAGGTGCCTCCAGTTGGTGCTTCAGCCCTGGCCCCTGTGGGGAAC A G AC010761.5 Ensembl:ENSG00000265840 lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs980702157 Functional Loss SNV dbSNP153 33..33 33 - - - 60637 RMVar_ID_60637 Human_SNP_ID_621224935 m1A Human chr17 + 28749736 28749736 28749736 CCTCCCCCAGCCACCACCCTCAGGTGCCTCCAATTGGTGCTTCAGCCCTGGCCCCTGTGGGGAAC CCTCCCCCAGCCACCACCCTCAGGTGCCTCCATTTGGTGCTTCAGCCCTGGCCCCTGTGGGGAAC A T AC010761.5 Ensembl:ENSG00000265840 lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs980702157 Functional Loss SNV dbSNP153 33..33 33 - - - 60638 RMVar_ID_60638 Human_SNP_ID_621230078 m1A Human chr17 + 28766688 28766688 28766688 ACAGGCTAGCATGGCAGATTGGCATCAACACAACATGGGGCAGTGGCTCACACTGTAATGAACAA ACAGGCTAGCATGGCAGATTGGCATCAACACAGCATGGGGCAGTGGCTCACACTGTAATGAACAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28766644..28766756 26863196 MeRIP-seq:(Medium) rs772612037 Functional Loss SNV dbSNP153 33..33 33 - - - 60639 RMVar_ID_60639 Human_SNP_ID_621230084 m1A Human chr17 - 28766709 28766709 28766709 TTGTGTTTCATGACCTTGTTTTTGTTCATTACAGTGTGAGCCACTGCCCCATGTTGTGTTGATGC TTGTGTTTCATGACCTTGTTTTTGTTCATTACCGTGTGAGCCACTGCCCCATGTTGTGTTGATGC T G FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28766658..28766750 26863196 MeRIP-seq:(Medium) rs769592494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899674,Human_RBP_ID_4465248 RMVar_hsa_circ_285541 60640 RMVar_ID_60640 Human_SNP_ID_621242242 m1A Human chr17 - 28812183 28812183 28812183 GCGCAAGGTGTGTGTGTGCTTTTTCTAACGCGACCCCGACTTCAGCCGACTTAACCTTGTAAGAA GCGCAAGGTGTGTGTGTGCTTTTTCTAACGCGTCCCCGACTTCAGCCGACTTAACCTTGTAAGAA T A FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28812177..28812370 26863196 MeRIP-seq:(Medium) rs756467382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2498783,Human_RBP_ID_3516591,Human_RBP_ID_12942008 Human_Splice_Rec_1797313 60641 RMVar_ID_60641 Human_SNP_ID_621242243 m1A Human chr17 - 28812183 28812183 28812183 GCGCAAGGTGTGTGTGTGCTTTTTCTAACGCGACCCCGACTTCAGCCGACTTAACCTTGTAAGAA GCGCAAGGTGTGTGTGTGCTTTTTCTAACGCGGCCCCGACTTCAGCCGACTTAACCTTGTAAGAA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28812177..28812370 26863196 MeRIP-seq:(Medium) rs756467382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2498783,Human_RBP_ID_3516591,Human_RBP_ID_12942008 Human_Splice_Rec_1797313 60642 RMVar_ID_60642 Human_SNP_ID_621242257 m1A Human chr17 - 28812218 28812218 28812218 ACGGAGCGCTGCGGAGCGAACCTCACCTTTCCAGGGCGCAAGGTGTGTGTGTGCTTTTTCTAACG ACGGAGCGCTGCGGAGCGAACCTCACCTTTCCGGGGCGCAAGGTGTGTGTGTGCTTTTTCTAACG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28812215..28812294 26863196 MeRIP-seq:(Medium) rs1327241490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3516591 Human_Splice_Rec_1797301,Human_Splice_Rec_1797313 60643 RMVar_ID_60643 Human_SNP_ID_621242526 m1A Human chr17 + 28813008 28813008 28813008 ATCCTCCCTGTCGGAAACTCGTGCTTCCCGTGACGCAGAAATTAAGCGGGGGGGGGGGGGGGGGG ATCCTCCCTGTCGGAAACTCGTGCTTCCCGTGGCGCAGAAATTAAGCGGGGGGGGGGGGGGGGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1310836119 Functional Loss SNV dbSNP153 33..33 33 - - - 60644 RMVar_ID_60644 Human_SNP_ID_621242544 m1A Human chr17 + 28813042 28813023 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCG___________________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1193278457 Functional Loss DEL dbSNP153 15..33 33 - - - 60645 RMVar_ID_60645 Human_SNP_ID_621242545 m1A Human chr17 + 28813042 28813024 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGG__________________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1489032152 Functional Loss DEL dbSNP153 16..33 33 - - - 60646 RMVar_ID_60646 Human_SNP_ID_621242547 m1A Human chr17 + 28813042 28813025 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGG_________________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1567874754 Functional Loss DEL dbSNP153 17..33 33 - - - 60647 RMVar_ID_60647 Human_SNP_ID_621242548 m1A Human chr17 + 28813042 28813026 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGG________________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1318129675 Functional Loss DEL dbSNP153 18..33 33 - - - 60648 RMVar_ID_60648 Human_SNP_ID_621242550 m1A Human chr17 + 28813042 28813027 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGG_______________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1485571980 Functional Loss DEL dbSNP153 19..33 33 - - - 60649 RMVar_ID_60649 Human_SNP_ID_621242551 m1A Human chr17 + 28813042 28813028 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGGG______________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1242016919 Functional Loss DEL dbSNP153 20..33 33 - - - 60650 RMVar_ID_60650 Human_SNP_ID_621242552 m1A Human chr17 + 28813042 28813029 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGGGG_____________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs869053812 Functional Loss DEL dbSNP153 21..33 33 - - - 60651 RMVar_ID_60651 Human_SNP_ID_621242555 m1A Human chr17 + 28813042 28813030 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGGGGG____________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1490424885 Functional Loss DEL dbSNP153 22..33 33 - - - 60652 RMVar_ID_60652 Human_SNP_ID_621242559 m1A Human chr17 + 28813042 28813041 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGG_GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1567874835 Functional Loss DEL dbSNP153 33..33 33 - - - 60653 RMVar_ID_60653 Human_SNP_ID_621242560 m1A Human chr17 + 28813042 28813042 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs914339894 Functional Loss SNV dbSNP153 33..33 33 - - - 60654 RMVar_ID_60654 Human_SNP_ID_621248257 m1A Human chr17 - 28834071 28834071 28834071 AGGAGAGTAACTAAAAGGATCTCATTGACTTTATATTGGAGGACGGGTAAAGAAGAAGGAGTTGT AGGAGAGTAACTAAAAGGATCTCATTGACTTTGTATTGGAGGACGGGTAAAGAAGAAGGAGTTGT T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28834064..28834157 26863196 MeRIP-seq:(Medium) rs1358309202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9850404,Human_RBP_ID_12942373 60655 RMVar_ID_60655 Human_SNP_ID_621250410 m1A Human chr17 - 28842201 28842201 28842201 GGTCTAGGGAAAAGAGCTAGGGGCTTAGAGTCAGGCAGGTTCGAAAGGAAGTCCACCATTGATAA GGTCTAGGGAAAAGAGCTAGGGGCTTAGAGTCCGGCAGGTTCGAAAGGAAGTCCACCATTGATAA T G FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28842199..28842277 26863196 MeRIP-seq:(Medium) rs1007098651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6573912,Human_RBP_ID_12942504,Human_RBP_ID_18941524,Human_RBP_ID_26782150 60656 RMVar_ID_60656 Human_SNP_ID_621250561 m1A Human chr17 - 28842719 28842719 28842719 TGGAGAAGTGGTGGCGGCGGGCGGCGGGCGGCAAAGGAGCAGCCATGAGGGCCGGGCCCAGTCAC TGGAGAAGTGGTGGCGGCGGGCGGCGGGCGGCGAAGGAGCAGCCATGAGGGCCGGGCCCAGTCAC T C FAM222B Ensembl:ENSG00000173065 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28842452..28842772 26863196 MeRIP-seq:(Medium) rs1041680674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6756,Human_RBP_ID_4465250,Human_RBP_ID_9422807,Human_RBP_ID_18420578 Human_Splice_Rec_1797293,Human_Splice_Rec_1797297,Human_Splice_Rec_1797305,Human_Splice_Rec_1797323,Human_Splice_Rec_1797329,Human_Splice_Rec_1797335,Human_Splice_Rec_1797345,Human_Splice_Rec_1797353,Human_Splice_Rec_1797363 60657 RMVar_ID_60657 Human_SNP_ID_621250562 m1A Human chr17 - 28842719 28842719 28842719 TGGAGAAGTGGTGGCGGCGGGCGGCGGGCGGCAAAGGAGCAGCCATGAGGGCCGGGCCCAGTCAC TGGAGAAGTGGTGGCGGCGGGCGGCGGGCGGCCAAGGAGCAGCCATGAGGGCCGGGCCCAGTCAC T G FAM222B Ensembl:ENSG00000173065 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28842452..28842772 26863196 MeRIP-seq:(Medium) rs1041680674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6756,Human_RBP_ID_4465250,Human_RBP_ID_9422807,Human_RBP_ID_18420578 Human_Splice_Rec_1797293,Human_Splice_Rec_1797297,Human_Splice_Rec_1797305,Human_Splice_Rec_1797323,Human_Splice_Rec_1797329,Human_Splice_Rec_1797335,Human_Splice_Rec_1797345,Human_Splice_Rec_1797353,Human_Splice_Rec_1797363 60658 RMVar_ID_60658 Human_SNP_ID_621250576 m1A Human chr17 + 28842740 28842740 28842740 GGCTGCTCCTTTGCCGCCCGCCGCCCGCCGCCACCACTTCTCCACTGCCCGGCCCCTCAGTCACC GGCTGCTCCTTTGCCGCCCGCCGCCCGCCGCCGCCACTTCTCCACTGCCCGGCCCCTCAGTCACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:28842454..28842773;chr17:28842370..28842772 26863196 MeRIP-seq:(Medium) rs1179971794 Functional Loss SNV dbSNP153 33..33 33 - - - 60659 RMVar_ID_60659 Human_SNP_ID_621255044 m1A Human chr17 + 28858682 28858681 28858682 AAAGCTCAAGATGAGGCAGGCCTTCCACTCACACCCTGGCACCCATTGCCCCAGCCCAGCAGTTA AAAGCTCAAGATGAGGCAGGCCTTCCACTCAC_CCCTGGCACCCATTGCCCCAGCCCAGCAGTTA CA C ERAL1 Ensembl:ENSG00000132591 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28858633..28858737 26863196 MeRIP-seq:(Medium) rs1452793294 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1006987,Human_RBP_ID_8447947,Human_RBP_ID_17258715,Human_RBP_ID_17888144,Human_RBP_ID_23718122,Human_RBP_ID_26813311,Human_RBP_ID_27450513 RMVar_hsa_circ_91655,RMVar_hsa_circ_94475,RMVar_hsa_circ_183024,RMVar_hsa_circ_100066,RMVar_hsa_circ_118765,RMVar_hsa_circ_121735,RMVar_hsa_circ_183025,RMVar_hsa_circ_336271,RMVar_hsa_circ_183027,RMVar_hsa_circ_101785,RMVar_hsa_circ_183026,RMVar_hsa_circ_108682,RMVar_hsa_circ_183028,RMVar_hsa_circ_330964,RMVar_hsa_circ_183029,RMVar_hsa_circ_183030 60660 RMVar_ID_60660 Human_SNP_ID_621255569 m1A Human chr17 - 28860510 28860510 28860510 GCTTCACAGAGAGGCGGATGTCAACATCGCAGAGGAAGATGTCCATGAGGTCATGGCCTGCCTCC GCTTCACAGAGAGGCGGATGTCAACATCGCAGGGGAAGATGTCCATGAGGTCATGGCCTGCCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28860406..28860551 26863196 MeRIP-seq:(Medium) rs1294952037 Functional Loss SNV dbSNP153 33..33 33 - - - 60661 RMVar_ID_60661 Human_SNP_ID_621260279 m1A Human chr17 + 28880336 28880336 28880336 AAGGAAAAGACACGCAGGGAGATGAGACACAAACCTGATGAAAGTGGCAGTGAAAGTGGGGTAAA AAGGAAAAGACACGCAGGGAGATGAGACACAAGCCTGATGAAAGTGGCAGTGAAAGTGGGGTAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28880286..28880473 26863196 MeRIP-seq:(Medium) rs1275866891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79188,RMVar_hsa_circ_183038 60662 RMVar_ID_60662 Human_SNP_ID_621260291 m1A Human chr17 + 28880393 28880393 28880393 GGGGTAAAGGAGAGGAAGAGGAGGAGGTGGACAGACAGGAGAGACAGGAAGACAGCCAGAGATGG GGGGTAAAGGAGAGGAAGAGGAGGAGGTGGACGGACAGGAGAGACAGGAAGACAGCCAGAGATGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28880376..28880500 26863196 MeRIP-seq:(Medium) rs1168770495 Functional Loss SNV dbSNP153 33..33 33 - - - 60663 RMVar_ID_60663 Human_SNP_ID_621260597 m1A Human chr17 - 28881328 28881328 28881328 CTTGGCACAGGCAGAGGCTGAGAAGATCCGCAAAATCGGGGAGGCGGAAGCGGCAGTCATCGAGG CTTGGCACAGGCAGAGGCTGAGAAGATCCGCACAATCGGGGAGGCGGAAGCGGCAGTCATCGAGG T G FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28881241..28881395 26863196 MeRIP-seq:(Medium) rs199774391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5187160,Human_RBP_ID_18990845 Human_Splice_Rec_1797476,Human_Splice_Rec_1797498,Human_Splice_Rec_1797518,Human_Splice_Rec_1797538,Human_Splice_Rec_1797558,Human_Splice_Rec_1797574,Human_Splice_Rec_1797590 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_121238,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183036,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60664 RMVar_ID_60664 Human_SNP_ID_621260774 m1A Human chr17 - 28881892 28881892 28881892 TGCCGTGGAGGCACAGGAGATCCTGCGTACGGACAAGGAGCTCATCGCTACAGTGCGCCGGCCTG TGCCGTGGAGGCACAGGAGATCCTGCGTACGGTCAAGGAGCTCATCGCTACAGTGCGCCGGCCTG T A FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28881842..28882025 26863196 MeRIP-seq:(Medium) rs1349628455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4414895,Human_RBP_ID_9289980,Human_RBP_ID_9340983,Human_RBP_ID_17888166,Human_RBP_ID_18191204 Human_Splice_Rec_1797475,Human_Splice_Rec_1797497,Human_Splice_Rec_1797517,Human_Splice_Rec_1797537,Human_Splice_Rec_1797557,Human_Splice_Rec_1797573,Human_Splice_Rec_1797589 Human_miRNA_ID_2894643 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60665 RMVar_ID_60665 Human_SNP_ID_621260804 m1A Human chr17 - 28881949 28881949 28881949 GCAGAAGATCCGGCAGGAAGAGATTGAGATTGAGGTTGTGCAGCGCAAGAAACAGATTGCCGTGG GCAGAAGATCCGGCAGGAAGAGATTGAGATTGGGGTTGTGCAGCGCAAGAAACAGATTGCCGTGG T C FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:28881801..28882050;chr17:28881801..28882250;chr17:28881851..28882050 26863196 MeRIP-seq:(Medium) rs749899892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_486042,Human_RBP_ID_12942587,Human_RBP_ID_17669953,Human_RBP_ID_17888167,Human_RBP_ID_23718140 Human_Splice_Rec_1797474,Human_Splice_Rec_1797496,Human_Splice_Rec_1797516,Human_Splice_Rec_1797536,Human_Splice_Rec_1797556,Human_Splice_Rec_1797572,Human_Splice_Rec_1797588,Human_Splice_Rec_1797598 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60666 RMVar_ID_60666 Human_SNP_ID_621260808 m1A Human chr17 - 28881959 28881959 28881959 CCCGTGAACAGCAGAAGATCCGGCAGGAAGAGATTGAGATTGAGGTTGTGCAGCGCAAGAAACAG CCCGTGAACAGCAGAAGATCCGGCAGGAAGAGGTTGAGATTGAGGTTGTGCAGCGCAAGAAACAG T C FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28881226..28882000 32194978 MeRIP-seq:(Medium) rs755576871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_486042,Human_RBP_ID_4414901,Human_RBP_ID_9345991,Human_RBP_ID_12942587,Human_RBP_ID_17669953,Human_RBP_ID_17888167 Human_Splice_Rec_1797474,Human_Splice_Rec_1797496,Human_Splice_Rec_1797516,Human_Splice_Rec_1797536,Human_Splice_Rec_1797556,Human_Splice_Rec_1797572,Human_Splice_Rec_1797588,Human_Splice_Rec_1797598 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60667 RMVar_ID_60667 Human_SNP_ID_621260880 m1A Human chr17 - 28882239 28882239 28882239 ACTCACCTTCCCCTTCTGCCCCTTTTGTCCCCAGGAAGCTGAGTGCAAGAAGGAGATGCTGGATG ACTCACCTTCCCCTTCTGCCCCTTTTGTCCCCCGGAAGCTGAGTGCAAGAAGGAGATGCTGGATG T G FLOT2 Ensembl:ENSG00000132589 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:28882101..28882250 26863196 MeRIP-seq:(Medium) rs770625552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899675 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60668 RMVar_ID_60668 Human_SNP_ID_621260913 m1A Human chr17 - 28882346 28882346 28882346 GACATTGGCGTGGCCGAGGCTGAACGGGACGCAGGCATCCGGGTATGTGGGTTCAAGGATGGGAA GACATTGGCGTGGCCGAGGCTGAACGGGACGCGGGCATCCGGGTATGTGGGTTCAAGGATGGGAA T C FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28882326..28882400 26863196 MeRIP-seq:(Medium) rs1231708523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8824577,Human_RBP_ID_9289981,Human_RBP_ID_18191205,Human_RBP_ID_22444444,Human_RBP_ID_22499054 Human_Splice_Rec_1797471,Human_Splice_Rec_1797493,Human_Splice_Rec_1797513,Human_Splice_Rec_1797533,Human_Splice_Rec_1797553,Human_Splice_Rec_1797569,Human_Splice_Rec_1797585,Human_Splice_Rec_1797595 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60669 RMVar_ID_60669 Human_SNP_ID_621260951 m1A Human chr17 - 28882449 28882449 28882449 TTGAGCCTCTGATACCCCCTTCCCTCCCCAGGACGTGTATGACAAAGTGGACTATCTGAGCTCCC TTGAGCCTCTGATACCCCCTTCCCTCCCCAGGGCGTGTATGACAAAGTGGACTATCTGAGCTCCC T C FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28882326..28882450 26863196 MeRIP-seq:(Medium) rs1469979776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1797470,Human_Splice_Rec_1797492,Human_Splice_Rec_1797512,Human_Splice_Rec_1797532,Human_Splice_Rec_1797552,Human_Splice_Rec_1797568,Human_Splice_Rec_1797584,Human_Splice_Rec_1797594 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 60670 RMVar_ID_60670 Human_SNP_ID_621261171 m1A Human chr17 - 28883228 28883228 28883228 AGCTGAAGCGCCTTTGTCGTCACTGACAGGTGAAGATCATGACGGAGAAGGAACTCCTGGCCGTG AGCTGAAGCGCCTTTGTCGTCACTGACAGGTGGAGATCATGACGGAGAAGGAACTCCTGGCCGTG T C FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28883090..28883266 26863196 MeRIP-seq:(Medium) rs763645724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6757,Human_RBP_ID_17904245,Human_RBP_ID_18191206,Human_RBP_ID_18990847,Human_RBP_ID_22587844,Human_RBP_ID_22656050,Human_RBP_ID_26813321 Human_Splice_Rec_1797466,Human_Splice_Rec_1797488,Human_Splice_Rec_1797508,Human_Splice_Rec_1797528,Human_Splice_Rec_1797548,Human_Splice_Rec_1797580,Human_Splice_Rec_1797581,Human_Splice_Rec_1797602,Human_Splice_Rec_1797608,Human_Splice_Rec_1797612 Human_miRNA_ID_2618107 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_110545,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161,RMVar_hsa_circ_115739,RMVar_hsa_circ_183040,RMVar_hsa_circ_183041 60671 RMVar_ID_60671 Human_SNP_ID_621261246 m1A Human chr17 + 28883491 28883491 28883491 GCCTCTCCTGGGCATTCGGGGCTTGTCTCCCCACCCCTCCAGCCTACTGTCCCCTCACCAGCTAA GCCTCTCCTGGGCATTCGGGGCTTGTCTCCCCCCCCCTCCAGCCTACTGTCCCCTCACCAGCTAA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:28883476..28883525 26863196 MeRIP-seq:(Medium) rs1273798475 Functional Loss SNV dbSNP153 33..33 33 - - - 60672 RMVar_ID_60672 Human_SNP_ID_621261434 m1A Human chr17 + 28884234 28884234 28884234 GCAGGGCTGCTGAGTTACTATACCTGGGCGACACCCGTCACAGTTAAAGCTACCCCCTCGGCCGT GCAGGGCTGCTGAGTTACTATACCTGGGCGACGCCCGTCACAGTTAAAGCTACCCCCTCGGCCGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28884226..28884346 26863196 MeRIP-seq:(Medium) rs1329991369 Functional Loss SNV dbSNP153 33..33 33 - - - 60673 RMVar_ID_60673 Human_SNP_ID_621264873 m1A Human chr17 + 28897618 28897618 28897618 CACGGAGGGCCCTCGGGACCGCACAGACCCGGACAACAGCAGCGGGTCTGCAGCGCCGGCCGCGC CACGGAGGGCCCTCGGGACCGCACAGACCCGGCCAACAGCAGCGGGTCTGCAGCGCCGGCCGCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:28897491..28897697;chr17:28897481..28897725;chr17:28897443..28897715 26863196 MeRIP-seq:(Medium) rs1302132820 Functional Loss SNV dbSNP153 33..33 33 - - - 60674 RMVar_ID_60674 Human_SNP_ID_621264889 m1A Human chr17 + 28897653 28897653 28897653 ACAGCAGCGGGTCTGCAGCGCCGGCCGCGCCCAGCCTATCCCGCCACCCCCAGCGGCCGGCCGCC ACAGCAGCGGGTCTGCAGCGCCGGCCGCGCCCGGCCTATCCCGCCACCCCCAGCGGCCGGCCGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:28897467..28897725 26863196 MeRIP-seq:(Medium) rs1447710978 Functional Loss SNV dbSNP153 33..33 33 - - - 60675 RMVar_ID_60675 Human_SNP_ID_621267505 m1A Human chr17 - 28906439 28906439 28906439 AGCCATGATGAGTTCCCAGGCCCAGGGGCCGCAGCGGAGACCCTGCAATTGCAAAGCCAGCAGCT AGCCATGATGAGTTCCCAGGCCCAGGGGCCGCGGCGGAGACCCTGCAATTGCAAAGCCAGCAGCT T C PHF12 Ensembl:ENSG00000109118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28906391..28906517 26863196 MeRIP-seq:(Medium) rs774453924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897458,Human_RBP_ID_3952052,Human_RBP_ID_27812445 Human_Splice_Rec_1797668,Human_Splice_Rec_1797698 Human_miRNA_ID_1310071 60676 RMVar_ID_60676 Human_SNP_ID_621269067 m1A Human chr17 - 28912668 28912668 28912668 TGCCCCCTTCCATTCCCAGCTCTTGTGCCAGCATCGAGAACACCAGCACTTTGCAAAGAAAGACT TGCCCCCTTCCATTCCCAGCTCTTGTGCCAGCGTCGAGAACACCAGCACTTTGCAAAGAAAGACT T C PHF12 Ensembl:ENSG00000109118 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28912617..28912702 26863196 MeRIP-seq:(Medium) rs986147977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899684,Human_RBP_ID_3950301,Human_RBP_ID_17888211,Human_RBP_ID_22061209,Human_RBP_ID_26331479,Human_RBP_ID_27252040 Human_miRNA_ID_1310073,Human_miRNA_ID_1685378,Human_miRNA_ID_1943265,Human_miRNA_ID_1943266,Human_miRNA_ID_1946310,Human_miRNA_ID_1946311,Human_miRNA_ID_2052439,Human_miRNA_ID_2052440,Human_miRNA_ID_2117456,Human_miRNA_ID_2117457,Human_miRNA_ID_2201038,Human_miRNA_ID_2201039,Human_miRNA_ID_2204101,Human_miRNA_ID_2204102,Human_miRNA_ID_2316647,Human_miRNA_ID_2316648,Human_miRNA_ID_2319803,Human_miRNA_ID_2319804,Human_miRNA_ID_2322959,Human_miRNA_ID_2322960,Human_miRNA_ID_2326132,Human_miRNA_ID_2326133,Human_miRNA_ID_2520509,Human_miRNA_ID_2520510,Human_miRNA_ID_2523672,Human_miRNA_ID_2523673,Human_miRNA_ID_2775510,Human_miRNA_ID_2775511,Human_miRNA_ID_2816559,Human_miRNA_ID_2816560,Human_miRNA_ID_2822861,Human_miRNA_ID_2822862,Human_miRNA_ID_2828995,Human_miRNA_ID_2828996,Human_miRNA_ID_2832153,Human_miRNA_ID_2832154,Human_miRNA_ID_2836273,Human_miRNA_ID_2836274,Human_miRNA_ID_2841628,Human_miRNA_ID_2841629,Human_miRNA_ID_2846682,Human_miRNA_ID_2846683,Human_miRNA_ID_2849707,Human_miRNA_ID_2849708,Human_miRNA_ID_2863822,Human_miRNA_ID_2863823,Human_miRNA_ID_3113555,Human_miRNA_ID_3113556 RMVar_hsa_circ_25517,RMVar_hsa_circ_62389,RMVar_hsa_circ_307792,RMVar_hsa_circ_64006,RMVar_hsa_circ_51189,RMVar_hsa_circ_183048,RMVar_hsa_circ_90398,RMVar_hsa_circ_183046,RMVar_hsa_circ_288633,RMVar_hsa_circ_183047,RMVar_hsa_circ_332417,RMVar_hsa_circ_268411,RMVar_hsa_circ_371490 60677 RMVar_ID_60677 Human_SNP_ID_621278114 m1A Human chr17 + 28950957 28950957 28950957 GTACACGATCGTCTTGGTCTCCATTTTCTCCCACATTCATCCACCTCCCGGGCTGGGTGCTCTCT GTACACGATCGTCTTGGTCTCCATTTTCTCCCCCATTCATCCACCTCCCGGGCTGGGTGCTCTCT A C PIPOX Ensembl:ENSG00000179761 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:28950858..28951185 26863196 MeRIP-seq:(Medium) rs1214044518 Functional Loss SNV dbSNP153 33..33 33 - - - 60678 RMVar_ID_60678 Human_SNP_ID_621278350 m1A Human chr17 - 28951431 28951431 28951431 AGTTTGCGCCAAGTGCGCGGCAGCCGGGACGCAGACGGCGGCGGCGGCGAGAGGCGGAGCCCGGG AGTTTGCGCCAAGTGCGCGGCAGCCGGGACGCGGACGGCGGCGGCGGCGAGAGGCGGAGCCCGGG T C PHF12 Ensembl:ENSG00000109118 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28951193..28951550 26863196 MeRIP-seq:(Medium) rs1197598077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47696,Human_RBP_ID_4415119,Human_RBP_ID_18419567 RMVar_hsa_circ_90398,RMVar_hsa_circ_183047 60679 RMVar_ID_60679 Human_SNP_ID_621308242 m1A Human chr17 - 29073620 29073620 29073620 GGAGCCCAAGTGCAGTGCCTGGTGCTGCTCCCATCTGCCGCCCCCCTTCTCTCCTGCAATTGGTT GGAGCCCAAGTGCAGTGCCTGGTGCTGCTCCCGTCTGCCGCCCCCCTTCTCTCCTGCAATTGGTT T C TIAF1,MYO18A Ensembl:ENSG00000221995,Ensembl:ENSG00000196535 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29073570..29073673 32194978 MeRIP-seq:(Medium) rs1440427749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115420,Human_RBP_ID_9377797,Human_RBP_ID_18692935,Human_RBP_ID_26457278 60680 RMVar_ID_60680 Human_SNP_ID_621311663 m1A Human chr17 - 29086492 29086492 29086492 AAAGTTGGCATTCAAGCGCATCGGGGACCTGCAGGCTGCCATTGAGGATGAGATGGAGAGTGATG AAAGTTGGCATTCAAGCGCATCGGGGACCTGCGGGCTGCCATTGAGGATGAGATGGAGAGTGATG T C MYO18A Ensembl:ENSG00000196535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29080984..29086554 32194978 MeRIP-seq:(Medium) rs1261321021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6574304,Human_RBP_ID_8815159,Human_RBP_ID_9375607,Human_RBP_ID_18990858,Human_RBP_ID_26331490,Human_RBP_ID_26457285 Human_Splice_Rec_1798222,Human_Splice_Rec_1798223,Human_Splice_Rec_1798236,Human_Splice_Rec_1798237,Human_Splice_Rec_1798314,Human_Splice_Rec_1798315,Human_Splice_Rec_1798394,Human_Splice_Rec_1798395,Human_Splice_Rec_1798472,Human_Splice_Rec_1798473,Human_Splice_Rec_1798552,Human_Splice_Rec_1798553,Human_Splice_Rec_1798566,Human_Splice_Rec_1798567,Human_Splice_Rec_1798575,Human_Splice_Rec_1798600 Human_miRNA_ID_1540578,Human_miRNA_ID_1594280 RMVar_hsa_circ_71497,RMVar_hsa_circ_59539,RMVar_hsa_circ_71390,RMVar_hsa_circ_25962 60681 RMVar_ID_60681 Human_SNP_ID_621313833 m1A Human chr17 - 29093930 29093930 29093930 TTACCTGTCCAGCGTAAACACCTGTTCCCATCACCGCTTTAAAGTAAGGGGCTTTCCACCTCCCT TTACCTGTCCAGCGTAAACACCTGTTCCCATCCCCGCTTTAAAGTAAGGGGCTTTCCACCTCCCT T G MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:29093926..29094100 26863196 MeRIP-seq:(Medium) rs1343023606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59539,RMVar_hsa_circ_267389 60682 RMVar_ID_60682 Human_SNP_ID_621314182 m1A Human chr17 - 29095027 29095024 29095027 GTTTGACAGTGAGCTCTCGCAGGCGCATGAGGAGGCCCAGCGGGAGAAGCTGCAGCGGGAGAAGC GTTTGACAGTGAGCTCTCGCAGGCGCATGAGG___CCCAGCGGGAGAAGCTGCAGCGGGAGAAGC GCCT G MYO18A Ensembl:ENSG00000196535 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:29094977..29095098 26863196 MeRIP-seq:(Medium) rs1231279562 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_896366,Human_RBP_ID_3952072,Human_RBP_ID_5525482,Human_RBP_ID_8815165,Human_RBP_ID_26331502 Human_Splice_Rec_1798202,Human_Splice_Rec_1798203,Human_Splice_Rec_1798296,Human_Splice_Rec_1798297,Human_Splice_Rec_1798374,Human_Splice_Rec_1798375,Human_Splice_Rec_1798452,Human_Splice_Rec_1798453,Human_Splice_Rec_1798532,Human_Splice_Rec_1798533,Human_Splice_Rec_1798604,Human_Splice_Rec_1798605 RMVar_hsa_circ_59539,RMVar_hsa_circ_267389 60683 RMVar_ID_60683 Human_SNP_ID_621314907 m1A Human chr17 + 29097758 29097758 29097758 AGGGGTGGGCATCAGGGCTCGCATTGCGGGCCACTGCCGAGCTCCTTGGGCCTCAGGCCCACCTG AGGGGTGGGCATCAGGGCTCGCATTGCGGGCCGCTGCCGAGCTCCTTGGGCCTCAGGCCCACCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:29097755..29097900 26863196 MeRIP-seq:(Medium) rs756345286 Functional Loss SNV dbSNP153 33..33 33 - - - 60684 RMVar_ID_60684 Human_SNP_ID_621315022 m1A Human chr17 - 29098061 29098061 29098061 GCCTGGGTGAGAACAGCAGGCTGGTGACTGCCATACCCTAGTGCCCATTGGCTCCCCCCAAAGAC GCCTGGGTGAGAACAGCAGGCTGGTGACTGCCGTACCCTAGTGCCCATTGGCTCCCCCCAAAGAC T C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29098059..29098182 26863196 MeRIP-seq:(Medium) rs752758761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19078699,Human_RBP_ID_22658600 RMVar_hsa_circ_59539 60685 RMVar_ID_60685 Human_SNP_ID_621315265 m1A Human chr17 - 29098790 29098789 29098790 TGTGACAGCCTGAGAGGGCCAAGTCTCTGGGTAGGGGGAAGCCTTGCTGGTTTATCTTGGGCTTC TGTGACAGCCTGAGAGGGCCAAGTCTCTGGGT_GGGGGAAGCCTTGCTGGTTTATCTTGGGCTTC CT C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:29098788..29098921 26863196 MeRIP-seq:(Medium) rs758148206 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_59539,RMVar_hsa_circ_44994 60686 RMVar_ID_60686 Human_SNP_ID_621321164 m1A Human chr17 - 29120755 29120753 29120756 TGATATCCCCTTGGGCCTGTATTCTGCAGTGGAGAAGTGGCAGGCTCTGTACACCCTCCTGGAAG TGATATCCCCTTGGGCCTGTATTCTGCAGTG___AAGTGGCAGGCTCTGTACACCCTCCTGGAAG TCTC T MYO18A Ensembl:ENSG00000196535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29114932..29121084 32194978 MeRIP-seq:(Medium) rs1274090053 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_897470,Human_RBP_ID_3950333,Human_RBP_ID_5363983,Human_RBP_ID_5526228 Human_Splice_Rec_1798158,Human_Splice_Rec_1798252,Human_Splice_Rec_1798330,Human_Splice_Rec_1798410,Human_Splice_Rec_1798488 RMVar_hsa_circ_37244,RMVar_hsa_circ_40901,RMVar_hsa_circ_30878,RMVar_hsa_circ_113258,RMVar_hsa_circ_183070,RMVar_hsa_circ_108638,RMVar_hsa_circ_330765,RMVar_hsa_circ_183072,RMVar_hsa_circ_183071,RMVar_hsa_circ_356770,RMVar_hsa_circ_359229,RMVar_hsa_circ_183074,RMVar_hsa_circ_63477,RMVar_hsa_circ_183073 60687 RMVar_ID_60687 Human_SNP_ID_621332061 m1A Human chr17 + 29166435 29166435 29166435 GATGCTGCACCAGCTGTCCCTCTAGAGTCCTCACCTCCACCTGTGGCGAGGGGGCGGCAGAGTGC GATGCTGCACCAGCTGTCCCTCTAGAGTCCTCCCCTCCACCTGTGGCGAGGGGGCGGCAGAGTGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29166251..29166502 32194978 MeRIP-seq:(Medium) rs1259788457 Functional Loss SNV dbSNP153 33..33 33 - - - 60688 RMVar_ID_60688 Human_SNP_ID_621363721 m1A Human chr17 + 29292614 29292613 29292614 CTACCCGAAATGAATCCCCCCGCCGCCCCCCCAGGCCTCCTGCCTCTAGGAGCGCCGCGGCCGCC CTACCCGAAATGAATCCCCCCGCCGCCCCCCC_GGCCTCCTGCCTCTAGGAGCGCCGCGGCCGCC CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:29292598..29292767 26863196 MeRIP-seq:(Medium) rs964434547 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_183079 60689 RMVar_ID_60689 Human_SNP_ID_621363725 m1A Human chr17 + 29292614 29292614 29292614 CTACCCGAAATGAATCCCCCCGCCGCCCCCCCAGGCCTCCTGCCTCTAGGAGCGCCGCGGCCGCC CTACCCGAAATGAATCCCCCCGCCGCCCCCCCCGGCCTCCTGCCTCTAGGAGCGCCGCGGCCGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:29292598..29292767 26863196 MeRIP-seq:(Medium) rs1486040695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183079 60690 RMVar_ID_60690 Human_SNP_ID_621363895 m1A Human chr17 - 29292902 29292892 29292902 CCCTGCACTGCGGGGGCGCCGGCGCCCCCCGCACCGCGGCCGCCCCCCCCCCCGTCGCCGGCCGG CCCTGCACTGCGGGGGCGCCGGCGCCCCCCGC__________CCCCCCCCCCCGTCGCCGGCCGG GCGGCCGCGGT G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr17:29292851..29292925;chr17:29292897..29293016 26863196 MeRIP-seq:(Medium) rs1047854734 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_5237885,Human_RBP_ID_26782158 60691 RMVar_ID_60691 Human_SNP_ID_621363902 m1A Human chr17 + 29292926 29292900 29292926 GGCCGCGGTGCGGGGGGCGCCGGCGCCCCCGCAGTGCAGGGGGCGAGGCTGCGGCCGGTGGTGAT GGCCGCG__________________________GTGCAGGGGGCGAGGCTGCGGCCGGTGGTGAT GGTGCGGGGGGCGCCGGCGCCCCCGCA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:29292876..29292925 26863196 MeRIP-seq:(Medium) rs1350037497 Functional Loss DEL dbSNP153 8..33 33 - - - RMVar_hsa_circ_183079 60692 RMVar_ID_60692 Human_SNP_ID_621363906 m1A Human chr17 - 29292902 29292902 29292902 CCCTGCACTGCGGGGGCGCCGGCGCCCCCCGCACCGCGGCCGCCCCCCCCCCCGTCGCCGGCCGG CCCTGCACTGCGGGGGCGCCGGCGCCCCCCGCCCCGCGGCCGCCCCCCCCCCCGTCGCCGGCCGG T G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr17:29292851..29292925;chr17:29292897..29293016 26863196 MeRIP-seq:(Medium) rs1042051661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5237885,Human_RBP_ID_26782158 60693 RMVar_ID_60693 Human_SNP_ID_621363919 m1A Human chr17 + 29292926 29292926 29292926 GGCCGCGGTGCGGGGGGCGCCGGCGCCCCCGCAGTGCAGGGGGCGAGGCTGCGGCCGGTGGTGAT GGCCGCGGTGCGGGGGGCGCCGGCGCCCCCGCGGTGCAGGGGGCGAGGCTGCGGCCGGTGGTGAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:29292876..29292925 26863196 MeRIP-seq:(Medium) rs567818794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183079 60694 RMVar_ID_60694 Human_SNP_ID_621364362 m1A Human chr17 - 29294036 29294036 29294036 CCGCTTTCAATGGAGGAGAAGCCCGGCCAGCCACAGCCTCAGCACCATCACAGCCACCACCATCC CCGCTTTCAATGGAGGAGAAGCCCGGCCAGCCGCAGCCTCAGCACCATCACAGCCACCACCATCC T C NUFIP2 Ensembl:ENSG00000108256 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:29293826..29294150;chr17:29293826..29294125;chr17:29293801..29294150 26863196 MeRIP-seq:(Medium) rs763952481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50369,Human_RBP_ID_768155,Human_RBP_ID_4415577,Human_RBP_ID_6575114,Human_RBP_ID_8448248,Human_RBP_ID_9375633,Human_RBP_ID_18419568,Human_RBP_ID_22061223,Human_RBP_ID_26331516 60695 RMVar_ID_60695 Human_SNP_ID_621388749 m1A Human chr17 + 29390542 29390542 29390542 CGCGAACATCTGAGGCCTCCCGGCCCCGGGGGACCCCGCCCCGCCGTCCGCCGGCCGGCCCGCGG CGCGAACATCTGAGGCCTCCCGGCCCCGGGGGCCCCCGCCCCGCCGTCCGCCGGCCGGCCCGCGG A C AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:29390424..29390675 26863196 MeRIP-seq:(Medium) rs983890741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820003,Human_RBP_ID_901735,Human_RBP_ID_3548347,Human_RBP_ID_4464435,Human_RBP_ID_5186488,Human_RBP_ID_18486444 Human_Splice_Rec_1798709 60696 RMVar_ID_60696 Human_SNP_ID_621431947 m1A Human chr17 - 29562560 29562560 29562560 TCTTTAACTGGAAGCGATCATACACAAGGTGAAAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA TCTTTAACTGGAAGCGATCATACACAAGGTGAGAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA T C ABHD15 Ensembl:ENSG00000168792 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs539307 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 60697 RMVar_ID_60697 Human_SNP_ID_621431948 m1A Human chr17 - 29562560 29562560 29562560 TCTTTAACTGGAAGCGATCATACACAAGGTGAAAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA TCTTTAACTGGAAGCGATCATACACAAGGTGACAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA T G ABHD15 Ensembl:ENSG00000168792 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs539307 Functional Loss SNV dbSNP153 33..33 33 - - - 60698 RMVar_ID_60698 Human_SNP_ID_621432082 m1A Human chr17 - 29562805 29562805 29562805 CAACCCCTACTTCTTCCTCCTGCTCAGTCGCCACGGAGGCCACTGTGGCTTCCTGCGCCAGGAGC CAACCCCTACTTCTTCCTCCTGCTCAGTCGCCTCGGAGGCCACTGTGGCTTCCTGCGCCAGGAGC T A ABHD15 Ensembl:ENSG00000168792 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:29562756..29562956 26863196 MeRIP-seq:(Medium) rs1198074038 Functional Loss SNV dbSNP153 33..33 33 - - - 60699 RMVar_ID_60699 Human_SNP_ID_621432135 m1A Human chr17 - 29562892 29562892 29562892 AGCCGTGCCTGTGCTGTGTATCTGCAGTGCTGACGACCCCGTGTGTGGACCCCCAGACCACACTC AGCCGTGCCTGTGCTGTGTATCTGCAGTGCTGGCGACCCCGTGTGTGGACCCCCAGACCACACTC T C ABHD15 Ensembl:ENSG00000168792 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29562741..29562891 32194978 MeRIP-seq:(Medium) rs1364542013 Functional Loss SNV dbSNP153 33..33 33 - - - 60700 RMVar_ID_60700 Human_SNP_ID_621433564 m1A Human chr17 + 29567264 29567263 29567264 GAGGGCGCGCCGGCAGCCGGAAGGGAGTGGGGAGGGCACGAGCCGGGGAGAGCGGTGTTGGCCAT GAGGGCGCGCCGGCAGCCGGAAGGGAGTGGGG_GGGCACGAGCCGGGGAGAGCGGTGTTGGCCAT GA G TP53I13,ABHD15-AS1 Ensembl:ENSG00000167543,Ensembl:ENSG00000264031 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29566570..29567361 26863196 MeRIP-seq:(Medium) rs530616489 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_819996,Human_RBP_ID_5098209,Human_RBP_ID_8193938,Human_RBP_ID_18419925,Human_RBP_ID_18988164,Human_RBP_ID_21974276 60701 RMVar_ID_60701 Human_SNP_ID_621434088 m1A Human chr17 - 29568832 29568832 29568832 GGGCCGAGGCCTTCCCAGGAGCGGGTCACCTTACCTCGCTGGGACCCAGGAGCCTCGCGAGGGCT GGGCCGAGGCCTTCCCAGGAGCGGGTCACCTTCCCTCGCTGGGACCCAGGAGCCTCGCGAGGGCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:29568730..29568850 26863410 MeRIP-seq:(Medium) rs752294319 Functional Loss SNV dbSNP153 33..33 33 - - - 60702 RMVar_ID_60702 Human_SNP_ID_621434191 m1A Human chr17 - 29569080 29569080 29569080 CTCCCTGGGCCCTCCAGGGCTCCTACCTGCGGAGGCAGAGGCCACAGGCTCTCGGGACAATGGGC CTCCCTGGGCCCTCCAGGGCTCCTACCTGCGGGGGCAGAGGCCACAGGCTCTCGGGACAATGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:29569029..29569179 32194978 MeRIP-seq:(Medium) rs1174655452 Functional Loss SNV dbSNP153 33..33 33 - - - 60703 RMVar_ID_60703 Human_SNP_ID_621435250 m1A Human chr17 + 29572519 29572511 29572520 GCTTCCCCGGCCCCTCGCGCAGCAGCGCCTCCACGGGCAGCCCGGGGCCCCACCCCACGCACTGA GCTTCCCCGGCCCCTCGCGCAGCAG_________GGGCAGCCCGGGGCCCCACCCCACGCACTGA GCGCCTCCAC G TP53I13,ABHD15-AS1 Ensembl:ENSG00000167543,Ensembl:ENSG00000264031 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29572471..29572717 26863196 MeRIP-seq:(Medium) rs1567763270 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_4470364,Human_RBP_ID_5098216,Human_RBP_ID_5188154 RMVar_hsa_circ_89808,RMVar_hsa_circ_183143 60704 RMVar_ID_60704 Human_SNP_ID_621435272 m1A Human chr17 - 29572549 29572549 29572549 GTCAGGGCCATGGCAGCCCAGGCGGCCTCTTCAGTGCGTGGGGTGGGGCCCCGGGCTGCCCGTGG GTCAGGGCCATGGCAGCCCAGGCGGCCTCTTCTGTGCGTGGGGTGGGGCCCCGGGCTGCCCGTGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:29572463..29572586 26863410 MeRIP-seq:(Medium) rs1159811564 Functional Loss SNV dbSNP153 33..33 33 - - - 60705 RMVar_ID_60705 Human_SNP_ID_621435502 m1A Human chr17 + 29572972 29572965 29572972 CACTGTGGCGTGCGGCTCCTCCCCGCGCCGCGAGGCCGCGACCTCTGCCACGTGGACCGCGCGCG CACTGTGGCGTGCGGCTCCTCCCCGC_______GGCCGCGACCTCTGCCACGTGGACCGCGCGCG CGCCGCGA C TP53I13,ABHD15-AS1 Ensembl:ENSG00000167543,Ensembl:ENSG00000264031 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29572812..29573024 26863196 MeRIP-seq:(Medium) rs989403622 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_899725,Human_RBP_ID_5115106,Human_RBP_ID_17654122,Human_RBP_ID_22443552 RMVar_hsa_circ_89808,RMVar_hsa_circ_183143 60706 RMVar_ID_60706 Human_SNP_ID_621435503 m1A Human chr17 + 29572972 29572965 29572973 CACTGTGGCGTGCGGCTCCTCCCCGCGCCGCGAGGCCGCGACCTCTGCCACGTGGACCGCGCGCG CACTGTGGCGTGCGGCTCCTCCCCGC________GCCGCGACCTCTGCCACGTGGACCGCGCGCG CGCCGCGAG C TP53I13,ABHD15-AS1 Ensembl:ENSG00000167543,Ensembl:ENSG00000264031 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29572812..29573024 26863196 MeRIP-seq:(Medium) rs1444451118 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_899725,Human_RBP_ID_5115106,Human_RBP_ID_17654122,Human_RBP_ID_22443552 RMVar_hsa_circ_89808,RMVar_hsa_circ_183143 60707 RMVar_ID_60707 Human_SNP_ID_621440472 m1A Human chr17 + 29589539 29589539 29589539 CGGCCAACCGTCCGCCCCGGGGCTGGCCCGGAACCCGCCGTGCCCGCCTGCCCGCTCGCCCTCGG CGGCCAACCGTCCGCCCCGGGGCTGGCCCGGACCCCGCCGTGCCCGCCTGCCCGCTCGCCCTCGG A C ABHD15-AS1 Ensembl:ENSG00000264031 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr17:29589451..29589608;chr17:29589490..29589606 26863410 MeRIP-seq:(Medium) rs901962156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5291144 60708 RMVar_ID_60708 Human_SNP_ID_621440489 m1A Human chr17 - 29589578 29589578 29589578 GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGAGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGGGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC T C GIT1 Ensembl:ENSG00000108262 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:29589248..29589634;chr17:29589236..29589650;chr17:29589490..29589631 26863196 MeRIP-seq:(Medium) rs998008746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262597,Human_RBP_ID_768158,Human_RBP_ID_4464451,Human_RBP_ID_5185108,Human_RBP_ID_18419926,Human_RBP_ID_26782162 60709 RMVar_ID_60709 Human_SNP_ID_621440490 m1A Human chr17 - 29589578 29589578 29589578 GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGAGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGCGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC T G GIT1 Ensembl:ENSG00000108262 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:29589248..29589634;chr17:29589236..29589650;chr17:29589490..29589631 26863196 MeRIP-seq:(Medium) rs998008746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262597,Human_RBP_ID_768158,Human_RBP_ID_4464451,Human_RBP_ID_5185108,Human_RBP_ID_18419926,Human_RBP_ID_26782162 60710 RMVar_ID_60710 Human_SNP_ID_621440510 m1A Human chr17 - 29589604 29589604 29589604 GAGCCGCGCAGGGGGCGGAGAGAGGAGCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGAGGGCGC GAGCCGCGCAGGGGGCGGAGAGAGGAGCCGCGGGCGGCGGCGGGGCGGCGCGGGGCGGAGGGCGC T C GIT1 Ensembl:ENSG00000108262 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:29589284..29589650;chr17:29589251..29589650;chr17:29589247..29589650 26863196 MeRIP-seq:(Medium) rs1190612766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768158,Human_RBP_ID_4464451,Human_RBP_ID_18419926,Human_RBP_ID_26782162 60711 RMVar_ID_60711 Human_SNP_ID_621441405 m1A Human chr17 - 29593195 29593195 29593195 CGCCCGCAGCCCCCGGGTCCCCACAGCTGCATAGCCCGGCCCTCAGCCCGAGCGGCCGGCGCGGG CGCCCGCAGCCCCCGGGTCCCCACAGCTGCATGGCCCGGCCCTCAGCCCGAGCGGCCGGCGCGGG T C GIT1 Ensembl:ENSG00000108262 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:29593057..29593327 26863196 MeRIP-seq:(Medium) rs1281945965 Functional Loss SNV dbSNP153 33..33 33 - - - 60712 RMVar_ID_60712 Human_SNP_ID_621441519 m1A Human chr17 - 29593492 29593492 29593492 CTGCTCGCGGGGCTGCGGCTCGGGCATGTGCGAGCGGCGGCGGGCGGGGGCGGCGCGCCCGGCGC CTGCTCGCGGGGCTGCGGCTCGGGCATGTGCGGGCGGCGGCGGGCGGGGGCGGCGCGCCCGGCGC T C GIT1 Ensembl:ENSG00000108262 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:29593483..29593610 26863196 MeRIP-seq:(Medium) rs1471107392 Functional Loss SNV dbSNP153 33..33 33 - - - 60713 RMVar_ID_60713 Human_SNP_ID_621447337 m1A Human chr17 + 29614406 29614406 29614406 GACACAAAGGGCTCGCCCAGGGCCCTGGCGCCACCCCCACCCCTTCCCACCAGCTGCTGCTAGCC GACACAAAGGGCTCGCCCAGGGCCCTGGCGCCCCCCCCACCCCTTCCCACCAGCTGCTGCTAGCC A C ABHD15-AS1,ANKRD13B Ensembl:ENSG00000264031,Ensembl:ENSG00000198720 lincRNA,Protein coding intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:29614358..29614537;chr17:29614355..29614539 26863196 MeRIP-seq:(Medium) rs1186965069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2052447,Human_miRNA_ID_2385605 RMVar_hsa_circ_95205,RMVar_hsa_circ_183159 60714 RMVar_ID_60714 Human_SNP_ID_621447360 m1A Human chr17 - 29614460 29614460 29614460 AAGGGTTTTAGAGTCAGTCTCCGTGTGGGGGCAAGTGGGATGTACAACCACAGAGGCTAGCAGCA AAGGGTTTTAGAGTCAGTCTCCGTGTGGGGGCCAGTGGGATGTACAACCACAGAGGCTAGCAGCA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:29614410..29614541 26863196 MeRIP-seq:(Medium) rs915342352 Functional Loss SNV dbSNP153 33..33 33 - - - 60715 RMVar_ID_60715 Human_SNP_ID_621449942 m1A Human chr17 - 29622752 29622752 29622752 CTCCTTCGCCCTGAAGCCTTCCTCGGCCCCCTACGCACTCGGGCCCCTTCCGCAGAGGATTCGCA CTCCTTCGCCCTGAAGCCTTCCTCGGCCCCCTTCGCACTCGGGCCCCTTCCGCAGAGGATTCGCA T A CORO6 Ensembl:ENSG00000167549 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:29622707..29622841 26863196 MeRIP-seq:(Medium) rs773559369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1799341,Human_Splice_Rec_1799361,Human_Splice_Rec_1799403,Human_Splice_Rec_1799447,Human_Splice_Rec_1799453,Human_Splice_Rec_1799461 60716 RMVar_ID_60716 Human_SNP_ID_621449943 m1A Human chr17 - 29622752 29622752 29622752 CTCCTTCGCCCTGAAGCCTTCCTCGGCCCCCTACGCACTCGGGCCCCTTCCGCAGAGGATTCGCA CTCCTTCGCCCTGAAGCCTTCCTCGGCCCCCTGCGCACTCGGGCCCCTTCCGCAGAGGATTCGCA T C CORO6 Ensembl:ENSG00000167549 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:29622707..29622841 26863196 MeRIP-seq:(Medium) rs773559369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1799341,Human_Splice_Rec_1799361,Human_Splice_Rec_1799403,Human_Splice_Rec_1799447,Human_Splice_Rec_1799453,Human_Splice_Rec_1799461 60717 RMVar_ID_60717 Human_SNP_ID_621485189 m1A Human chr17 - 29773071 29773071 29773071 GGATGATGGATGGATGGGTGGATGATGGATGGATGGGTGGATGATGGATGGATGGATGGATGGAT GGATGATGGATGGATGGGTGGATGATGGATGGGTGGGTGGATGATGGATGGATGGATGGATGGAT T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:29773046..29773167 26863196 MeRIP-seq:(Medium) rs62068613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648472 RMVar_hsa_circ_4443,RMVar_hsa_circ_101763,RMVar_hsa_circ_183163,RMVar_hsa_circ_75661,RMVar_hsa_circ_125995,RMVar_hsa_circ_183197,RMVar_hsa_circ_183208,RMVar_hsa_circ_183196,RMVar_hsa_circ_376304,RMVar_hsa_circ_26469 60718 RMVar_ID_60718 Human_SNP_ID_621518482 m1A Human chr17 + 29929780 29929780 29929780 GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTAGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTCGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG A C EFCAB5 Ensembl:ENSG00000176927 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:29929777..29929909 26863196 MeRIP-seq:(Medium) rs867530617 Functional Loss SNV dbSNP153 33..33 33 - - - 60719 RMVar_ID_60719 Human_SNP_ID_621518483 m1A Human chr17 + 29929780 29929780 29929780 GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTAGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTGGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG A G EFCAB5 Ensembl:ENSG00000176927 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:29929777..29929909 26863196 MeRIP-seq:(Medium) rs867530617 Functional Loss SNV dbSNP153 33..33 33 - - - 60720 RMVar_ID_60720 Human_SNP_ID_621518484 m1A Human chr17 + 29929780 29929780 29929780 GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTAGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG GCAAAAATCAACGTCTTGTAGTTCCTGCTGCTTGTCTTTAACATGGGGGTGTGGGGGGGTTCGCG A T EFCAB5 Ensembl:ENSG00000176927 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:29929777..29929909 26863196 MeRIP-seq:(Medium) rs867530617 Functional Loss SNV dbSNP153 33..33 33 - - - 60721 RMVar_ID_60721 Human_SNP_ID_621518592 m1A Human chr17 - 29930042 29930042 29930042 CCGGCTCCGTCACCCTCCCGTCCCCCACACTCAGGACAAGAATGCCCTGCCCGGAACAACCCAGC CCGGCTCCGTCACCCTCCCGTCCCCCACACTCTGGACAAGAATGCCCTGCCCGGAACAACCCAGC T A SSH2 Ensembl:ENSG00000141298 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:29929864..29930184 26863196 MeRIP-seq:(Medium) rs1383055624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129108,Human_RBP_ID_5441282,Human_RBP_ID_12950952,Human_RBP_ID_17079541,Human_RBP_ID_17378257,Human_RBP_ID_17566410,Human_RBP_ID_18941554,Human_RBP_ID_26448769 Human_miRNA_ID_655715,Human_miRNA_ID_1770683 60722 RMVar_ID_60722 Human_SNP_ID_621518630 m1A Human chr17 - 29930148 29930148 29930148 GTCAGTCGGCGACAGTCTGGTGGTGGGTGCGGAGTCTGCGGCCGTTCCCGCGGCCTCCTCCTCCT GTCAGTCGGCGACAGTCTGGTGGTGGGTGCGGGGTCTGCGGCCGTTCCCGCGGCCTCCTCCTCCT T C SSH2 Ensembl:ENSG00000141298 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:29930051..29930225 26863410 MeRIP-seq:(Medium) rs1271475841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23719149 60723 RMVar_ID_60723 Human_SNP_ID_399750464 m1A Human chr9 + 61330863 61330863 61330863 CGTGAGGAAGAGAGCTAGAGACTGGACACGGGAGACAGAGCAGCGTCAGAGCCGCGCAGGGGACG CGTGAGGAAGAGAGCTAGAGACTGGACACGGGTGACAGAGCAGCGTCAGAGCCGCGCAGGGGACG A T CNTNAP3C Ensembl:ENSG00000283378 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:61330810..61330914;chr9:61330788..61330914;chr9:61330807..61330915 26863196 MeRIP-seq:(Medium) rs1313574712 Functional Loss SNV dbSNP153 33..33 33 - - - 60724 RMVar_ID_60724 Human_SNP_ID_399868525 m1A Human chr9 + 61917489 61917489 61917489 TGTTTTTACAGAGACGAGGTCTCACTATATTGACCAGGCTGGTCTTGAACTCCTGGCCTTAAGCG TGTTTTTACAGAGACGAGGTCTCACTATATTGCCCAGGCTGGTCTTGAACTCCTGGCCTTAAGCG A C FAM27C Ensembl:ENSG00000231527 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:61917430..61917504 26863196 MeRIP-seq:(Medium) rs691041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1047112,Human_Splice_Rec_1047120,Human_Splice_Rec_1047132,Human_Splice_Rec_1047136,Human_Splice_Rec_1047144,Human_Splice_Rec_1047146,Human_Splice_Rec_1047152,Human_Splice_Rec_1047156,Human_Splice_Rec_1047164,Human_Splice_Rec_1047168,Human_Splice_Rec_1047172,Human_Splice_Rec_1047176,Human_Splice_Rec_1047182,Human_Splice_Rec_1047188,Human_Splice_Rec_1047202,Human_Splice_Rec_1047214,Human_Splice_Rec_1047220,Human_Splice_Rec_1047224,Human_Splice_Rec_1047230,Human_Splice_Rec_1047236,Human_Splice_Rec_1047242 60725 RMVar_ID_60725 Human_SNP_ID_399974808 m1A Human chr9 - 62799589 62799588 62799590 TCCACCTTGCTCTCTCTCTCTCTCTCTCTCTCAATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA TCCACCTTGCTCTCTCTCTCTCTCTCTCTCT__ATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA TTG T lnc-FOXD4L5-27,lnc-FOXD4L5-27:2 RNACentral:URS00008C163A,RNACentral:URS00009AE1AE lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1564073194 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1118736 60726 RMVar_ID_60726 Human_SNP_ID_399974810 m1A Human chr9 - 62799589 62799589 62799589 TCCACCTTGCTCTCTCTCTCTCTCTCTCTCTCAATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA TCCACCTTGCTCTCTCTCTCTCTCTCTCTCTCTATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA T A lnc-FOXD4L5-27,lnc-FOXD4L5-27:2 RNACentral:URS00008C163A,RNACentral:URS00009AE1AE lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7032037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1118736 60727 RMVar_ID_60727 Human_SNP_ID_400003618 m1A Human chr9 - 62897749 62897749 62897749 AGGCCGGGGAAGGCGCCGGTGGGAGGCAAGGCACGGATGGACTTTACCTGCGCACGCGTCGCAGC AGGCCGGGGAAGGCGCCGGTGGGAGGCAAGGCTCGGATGGACTTTACCTGCGCACGCGTCGCAGC T A LERFS Ensembl:ENSG00000234665 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:62897747..62897886 26863196 MeRIP-seq:(Medium) rs7028248 Functional Loss SNV dbSNP153 33..33 33 - - - 60728 RMVar_ID_60728 Human_SNP_ID_400003619 m1A Human chr9 - 62897749 62897749 62897749 AGGCCGGGGAAGGCGCCGGTGGGAGGCAAGGCACGGATGGACTTTACCTGCGCACGCGTCGCAGC AGGCCGGGGAAGGCGCCGGTGGGAGGCAAGGCGCGGATGGACTTTACCTGCGCACGCGTCGCAGC T C LERFS Ensembl:ENSG00000234665 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:62897747..62897886 26863196 MeRIP-seq:(Medium) rs7028248 Functional Loss SNV dbSNP153 33..33 33 - - - 60729 RMVar_ID_60729 Human_SNP_ID_400627215 m1A Human chr9 + 65675977 65675977 65675977 TCAGCTGAGGTAGGGACGTGCCGTAGGCCGGAATGTTACCGGCTGTTGGATCTGTGGATGAGGAA TCAGCTGAGGTAGGGACGTGCCGTAGGCCGGAGTGTTACCGGCTGTTGGATCTGTGGATGAGGAA A G CBWD5 Ensembl:ENSG00000147996 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:65675926..65676030;chr9:65675926..65676033 26863196 MeRIP-seq:(Medium) rs778893007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036182,Human_RBP_ID_5431262,Human_RBP_ID_18427149,Human_RBP_ID_24305599,Human_RBP_ID_27843843 60730 RMVar_ID_60730 Human_SNP_ID_400653461 m1A Human chr9 + 65825672 65825654 65825672 CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGACGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG CGGCGGCGAGGCGGG__________________CGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG GCGGCGGCGGCGAGGCGGA G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:65825606..65825688 26863410 MeRIP-seq:(Medium) rs1216478553 Functional Loss DEL dbSNP153 16..33 33 - - - 60731 RMVar_ID_60731 Human_SNP_ID_400653474 m1A Human chr9 + 65825672 65825670 65825673 CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGACGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCG___GGCGGCGGCGCGGCGGAGAGGCGCACAGCCG GGAC G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:65825606..65825688 26863410 MeRIP-seq:(Medium) rs1473715813 Functional Loss DEL dbSNP153 32..34 33 - - - 60732 RMVar_ID_60732 Human_SNP_ID_400653476 m1A Human chr9 + 65825672 65825672 65825672 CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGACGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGCCGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:65825606..65825688 26863410 MeRIP-seq:(Medium) rs1182968936 Functional Loss SNV dbSNP153 33..33 33 - - - 60733 RMVar_ID_60733 Human_SNP_ID_400653477 m1A Human chr9 + 65825672 65825672 65825672 CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGACGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGGCGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:65825606..65825688 26863410 MeRIP-seq:(Medium) rs1182968936 Functional Loss SNV dbSNP153 33..33 33 - - - 60734 RMVar_ID_60734 Human_SNP_ID_400653478 m1A Human chr9 + 65825672 65825672 65825672 CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGACGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG CGGCGGCGAGGCGGGCGGCGGCGGCGAGGCGGTCGGCGGCGGCGCGGCGGAGAGGCGCACAGCCG A T - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:65825606..65825688 26863410 MeRIP-seq:(Medium) rs1182968936 Functional Loss SNV dbSNP153 33..33 33 - - - 60735 RMVar_ID_60735 Human_SNP_ID_400970573 m1A Human chr9 - 67725679 67725679 67725679 TCCCTGTCACTGGAACGCTGGCCTCCCTGGACAAGCCACCCTTTAGGAACCCCACCCCTTATGTC TCCCTGTCACTGGAACGCTGGCCTCCCTGGACGAGCCACCCTTTAGGAACCCCACCCCTTATGTC T C FAM27B RNACentral:URS000075BE29 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1210449291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22118122,Human_RBP_ID_27137066 60736 RMVar_ID_60736 Human_SNP_ID_401141005 m1A Human chr9 - 68780134 68780134 68780134 ATGTCGGGGGCAGGGAGGCGGGGGAGGTGCTCAGTCAGGGACCTAGGATTCCCATTCCCCGCAGT ATGTCGGGGGCAGGGAGGCGGGGGAGGTGCTCGGTCAGGGACCTAGGATTCCCATTCCCCGCAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:68780083..68780441;chr9:68780083..68780389 26863196 MeRIP-seq:(Medium) rs1467136194 Functional Loss SNV dbSNP153 33..33 33 - - - 60737 RMVar_ID_60737 Human_SNP_ID_401199051 m1A Human chr9 + 69035836 69035836 69035836 GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCAGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCGGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:69035786..69035950 26863196 MeRIP-seq:(Medium) rs2481598 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5036779 Clinvar_Rec_214 GWAS_ID_7357 60738 RMVar_ID_60738 Human_SNP_ID_401199052 m1A Human chr9 + 69035836 69035836 69035836 GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCAGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCTGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG A T AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:69035786..69035950 26863196 MeRIP-seq:(Medium) rs2481598 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5036779 Clinvar_Rec_214 GWAS_ID_7357 60739 RMVar_ID_60739 Human_SNP_ID_401199057 m1A Human chr9 + 69035849 69035849 69035849 TCCTGGCGTCACCCAGCCCAGCCCAGGCCCAGACCCTCACCCGGGTCCCGCGGCCGGCAGAGTTG TCCTGGCGTCACCCAGCCCAGCCCAGGCCCAGGCCCTCACCCGGGTCCCGCGGCCGGCAGAGTTG A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:69035801..69035932 26863196 MeRIP-seq:(Medium) rs777206398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036779 Human_Splice_Rec_1049591,Human_Splice_Rec_1049599,Human_Splice_Rec_1049605,Human_Splice_Rec_1049613,Human_Splice_Rec_1049643,Human_Splice_Rec_1049653,Human_Splice_Rec_1049699,Human_Splice_Rec_1049747,Human_Splice_Rec_1049795,Human_Splice_Rec_1049805,Human_Splice_Rec_1049811 60740 RMVar_ID_60740 Human_SNP_ID_401220595 m1A Human chr9 + 69121343 69121343 69121343 TGCGTCTCCCTCCCGGGGCTCGCGCGCCCAGAACCCTCCGGTCTCAAGGAAGCAGGTGACAGCCG TGCGTCTCCCTCCCGGGGCTCGCGCGCCCAGACCCCTCCGGTCTCAAGGAAGCAGGTGACAGCCG A C TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69121292..69121433 26863196 MeRIP-seq:(Medium) rs1564361405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9408067 Human_Splice_Rec_1049825,Human_Splice_Rec_1049829,Human_Splice_Rec_1049871,Human_Splice_Rec_1049873 60741 RMVar_ID_60741 Human_SNP_ID_401222476 m1A Human chr9 + 69130672 69130672 69130672 GCTTGAGGCTGGTCTGGGCATCCTGTGTGTGCAGGGGCTTGGTGGAGCTGTGGAAGTGGGTACCA GCTTGAGGCTGGTCTGGGCATCCTGTGTGTGCCGGGGCTTGGTGGAGCTGTGGAAGTGGGTACCA A C TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:69130659..69130911 26863196 MeRIP-seq:(Medium) rs938727529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17175718,Human_RBP_ID_21995833 60742 RMVar_ID_60742 Human_SNP_ID_401233317 m1A Human chr9 - 69174336 69174336 69174336 GACACAGGTCCCGCGTAGGCGCGCAGCTCCGGACCCCGCTTCTGCTTCTGCTCCTGCTCCTACTC GACACAGGTCCCGCGTAGGCGCGCAGCTCCGGGCCCCGCTTCTGCTTCTGCTCCTGCTCCTACTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69174200..69174355 26863196 MeRIP-seq:(Medium) rs758922783 Functional Loss SNV dbSNP153 33..33 33 - - - 60743 RMVar_ID_60743 Human_SNP_ID_401233354 m1A Human chr9 - 69174397 69174396 69174398 GAGCCAACCTGACAGCTCCCGCCGGGGTGGAAACCCGCGGTCTCCTCGCACCGGCATTTCGGACA GAGCCAACCTGACAGCTCCCGCCGGGGTGGA__CCCGCGGTCTCCTCGCACCGGCATTTCGGACA GTT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:69174307..69204823 32194978 MeRIP-seq:(Medium) rs1294085720 Functional Loss DEL dbSNP153 32..33 33 - - - 60744 RMVar_ID_60744 Human_SNP_ID_401245303 m1A Human chr9 - 69220985 69220985 69220985 CTCTCGCTGTAGCCACTCCGGAAACTTCTGCCATCAAACTCGTCCATCACCTCAAAAGCCCGGTC CTCTCGCTGTAGCCACTCCGGAAACTTCTGCCGTCAAACTCGTCCATCACCTCAAAAGCCCGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69220935..69221176 26863196 MeRIP-seq:(Medium) rs924760397 Functional Loss SNV dbSNP153 33..33 33 - - - 60745 RMVar_ID_60745 Human_SNP_ID_401253245 m1A Human chr9 + 69249483 69249483 69249483 GCCCGCCCCCAGCATTCAAGCCAGAGCCGCCCAAGGTACGTGGCTGGGAAGCCCAGGATGGGAAG GCCCGCCCCCAGCATTCAAGCCAGAGCCGCCCCAGGTACGTGGCTGGGAAGCCCAGGATGGGAAG A C TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:69249450..69251100 32194978 MeRIP-seq:(Medium) rs775892454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962064,Human_RBP_ID_5408331,Human_RBP_ID_18472655,Human_RBP_ID_19143419,Human_RBP_ID_22691120 Human_Splice_Rec_1049789,Human_Splice_Rec_1050003,Human_Splice_Rec_1050093,Human_Splice_Rec_1050251,Human_Splice_Rec_1050461,Human_Splice_Rec_1050505,Human_Splice_Rec_1050601 RMVar_hsa_circ_54414,RMVar_hsa_circ_121491,RMVar_hsa_circ_257026,RMVar_hsa_circ_345034,RMVar_hsa_circ_86179,RMVar_hsa_circ_21105,RMVar_hsa_circ_257027,RMVar_hsa_circ_366411,RMVar_hsa_circ_364840,RMVar_hsa_circ_353528,RMVar_hsa_circ_374548,RMVar_hsa_circ_257030 60746 RMVar_ID_60746 Human_SNP_ID_401253246 m1A Human chr9 + 69249483 69249483 69249483 GCCCGCCCCCAGCATTCAAGCCAGAGCCGCCCAAGGTACGTGGCTGGGAAGCCCAGGATGGGAAG GCCCGCCCCCAGCATTCAAGCCAGAGCCGCCCGAGGTACGTGGCTGGGAAGCCCAGGATGGGAAG A G TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:69249450..69251100 32194978 MeRIP-seq:(Medium) rs775892454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962064,Human_RBP_ID_5408331,Human_RBP_ID_18472655,Human_RBP_ID_19143419,Human_RBP_ID_22691120 Human_Splice_Rec_1049789,Human_Splice_Rec_1050003,Human_Splice_Rec_1050093,Human_Splice_Rec_1050251,Human_Splice_Rec_1050461,Human_Splice_Rec_1050505,Human_Splice_Rec_1050601 RMVar_hsa_circ_54414,RMVar_hsa_circ_121491,RMVar_hsa_circ_257026,RMVar_hsa_circ_345034,RMVar_hsa_circ_86179,RMVar_hsa_circ_21105,RMVar_hsa_circ_257027,RMVar_hsa_circ_366411,RMVar_hsa_circ_364840,RMVar_hsa_circ_353528,RMVar_hsa_circ_374548,RMVar_hsa_circ_257030 60747 RMVar_ID_60747 Human_SNP_ID_401254517 m1A Human chr9 + 69254307 69254307 69254307 CAGTGATGCCGAGGAGGAGGAGTACCGCCAGCAGCTGTCAGAACACTCCAAGCGCGGTTACTATG CAGTGATGCCGAGGAGGAGGAGTACCGCCAGCGGCTGTCAGAACACTCCAAGCGCGGTTACTATG A G TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:69254257..69254408 32194978 MeRIP-seq:(Medium) rs547489209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9315094,Human_RBP_ID_23120881 Human_Splice_Rec_1049794,Human_Splice_Rec_1049870,Human_Splice_Rec_1050008,Human_Splice_Rec_1050054,Human_Splice_Rec_1050098,Human_Splice_Rec_1050298,Human_Splice_Rec_1050332,Human_Splice_Rec_1050374,Human_Splice_Rec_1050422,Human_Splice_Rec_1050466,Human_Splice_Rec_1050510,Human_Splice_Rec_1050554,Human_Splice_Rec_1050590,Human_Splice_Rec_1050604 Human_miRNA_ID_97287,Human_miRNA_ID_97288 60748 RMVar_ID_60748 Human_SNP_ID_401272141 m1A Human chr9 - 69325229 69325229 69325229 GAGGACGCGGAGCGGAGCCGAGCCGAAGGCGCAGCACACTGGGCACTGCAGACGGGCTCCGAGGC GAGGACGCGGAGCGGAGCCGAGCCGAAGGCGCGGCACACTGGGCACTGCAGACGGGCTCCGAGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69325186..69325419 26863196 MeRIP-seq:(Medium) rs1388158708 Functional Loss SNV dbSNP153 33..33 33 - - - 60749 RMVar_ID_60749 Human_SNP_ID_401288333 m1A Human chr9 + 69391700 69391700 69391700 TGCTGCACCTCCAGAGCTGCGGCGACCTTCACACCTTCACACCAGCGGGGAGGCCCCGAGCCGAG TGCTGCACCTCCAGAGCTGCGGCGACCTTCACCCCTTCACACCAGCGGGGAGGCCCCGAGCCGAG A C FAM189A2 Ensembl:ENSG00000135063 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69391651..69391789 26863196 MeRIP-seq:(Medium) rs773511736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1050644,Human_Splice_Rec_1050662,Human_Splice_Rec_1050682,Human_Splice_Rec_1050702,Human_Splice_Rec_1050718,Human_Splice_Rec_1050730,Human_Splice_Rec_1050742,Human_Splice_Rec_1050764 RMVar_hsa_circ_257031,RMVar_hsa_circ_75659 60750 RMVar_ID_60750 Human_SNP_ID_401288334 m1A Human chr9 + 69391700 69391700 69391700 TGCTGCACCTCCAGAGCTGCGGCGACCTTCACACCTTCACACCAGCGGGGAGGCCCCGAGCCGAG TGCTGCACCTCCAGAGCTGCGGCGACCTTCACGCCTTCACACCAGCGGGGAGGCCCCGAGCCGAG A G FAM189A2 Ensembl:ENSG00000135063 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69391651..69391789 26863196 MeRIP-seq:(Medium) rs773511736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1050644,Human_Splice_Rec_1050662,Human_Splice_Rec_1050682,Human_Splice_Rec_1050702,Human_Splice_Rec_1050718,Human_Splice_Rec_1050730,Human_Splice_Rec_1050742,Human_Splice_Rec_1050764 RMVar_hsa_circ_257031,RMVar_hsa_circ_75659 60751 RMVar_ID_60751 Human_SNP_ID_401374811 m1A Human chr9 + 69759904 69759904 69759904 AGGCGTTAGTGATGTCCTTCACAACCCGCTGCACCAGCACCGCCACCTCCTCGCTGGTCTCGGCC AGGCGTTAGTGATGTCCTTCACAACCCGCTGCCCCAGCACCGCCACCTCCTCGCTGGTCTCGGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:69759805..69759923 26863196 MeRIP-seq:(Medium) rs781265092 Functional Loss SNV dbSNP153 33..33 33 - - - 60752 RMVar_ID_60752 Human_SNP_ID_401374812 m1A Human chr9 + 69759904 69759904 69759904 AGGCGTTAGTGATGTCCTTCACAACCCGCTGCACCAGCACCGCCACCTCCTCGCTGGTCTCGGCC AGGCGTTAGTGATGTCCTTCACAACCCGCTGCGCCAGCACCGCCACCTCCTCGCTGGTCTCGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:69759805..69759923 26863196 MeRIP-seq:(Medium) rs781265092 Functional Loss SNV dbSNP153 33..33 33 - - - 60753 RMVar_ID_60753 Human_SNP_ID_401439620 m1A Human chr9 - 70030766 70030761 70030766 AGGAAGGAAAAGAAAAGAAGAAAGGAAAGGAAAGGAAGGAAGGAAAAGAAAAGAAAAACCTGATA AGGAAGGAAAAGAAAAGAAGAAAGGAAAGGAA_____GGAAGGAAAAGAAAAGAAAAACCTGATA CTTCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70030736..70030842 26863196 MeRIP-seq:(Medium) rs1192427061 Functional Loss DEL dbSNP153 33..37 33 - - - 60754 RMVar_ID_60754 Human_SNP_ID_401439623 m1A Human chr9 - 70030766 70030766 70030766 AGGAAGGAAAAGAAAAGAAGAAAGGAAAGGAAAGGAAGGAAGGAAAAGAAAAGAAAAACCTGATA AGGAAGGAAAAGAAAAGAAGAAAGGAAAGGAAGGGAAGGAAGGAAAAGAAAAGAAAAACCTGATA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70030736..70030842 26863196 MeRIP-seq:(Medium) rs58236988 Functional Loss SNV dbSNP153 33..33 33 - - - 60755 RMVar_ID_60755 Human_SNP_ID_401441393 m1A Human chr9 + 70038209 70038209 70038209 GGAATTGAATGGAATGCAATAGAATGGAATGGAATCAACTCGAGTGGAATGGAATGGAATGGAAT GGAATTGAATGGAATGCAATAGAATGGAATGGTATCAACTCGAGTGGAATGGAATGGAATGGAAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:70038151..70038438 26863196 MeRIP-seq:(Medium) rs895646249 Functional Loss SNV dbSNP153 33..33 33 - - - 60756 RMVar_ID_60756 Human_SNP_ID_401455252 m1A Human chr9 + 70100015 70100015 70100015 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCACAAGCACAATGGGCAGCAGGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGAGAGAGAGCACAAGCACAATGGGCAGCAGGT A T MAMDC2 Ensembl:ENSG00000165072 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70100013..70100123 26863196 MeRIP-seq:(Medium) rs895188746 Functional Loss SNV dbSNP153 33..33 33 - - - 60757 RMVar_ID_60757 Human_SNP_ID_401479352 m1A Human chr9 - 70204832 70204832 70204832 GGAGTTCCCTTTCCAAGTCAAAGAAAGGGGTGAAGGACACACCTGGAAAATCGGGTCACTCCCAC GGAGTTCCCTTTCCAAGTCAAAGAAAGGGGTGGAGGACACACCTGGAAAATCGGGTCACTCCCAC T C SMC5-AS1 Ensembl:ENSG00000268364 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:70204782..70204914 26863196 MeRIP-seq:(Medium) rs1229094408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257060,RMVar_hsa_circ_257061 60758 RMVar_ID_60758 Human_SNP_ID_401482193 m1A Human chr9 - 70214234 70214222 70214234 AGACCTGTTCTGACTATACTATTCCAAATTGCAGTCCCTCTTCCCTGGCACTCCTCATTCCTTAT AGACCTGTTCTGACTATACTATTCCAAATTGC____________CTGGCACTCCTCATTCCTTAT GGGAAGAGGGACT G SMC5-AS1 Ensembl:ENSG00000268364 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70214189..70214345 26863196 MeRIP-seq:(Medium) rs1478677147 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_5107154 RMVar_hsa_circ_257060,RMVar_hsa_circ_257061 60759 RMVar_ID_60759 Human_SNP_ID_401482203 m1A Human chr9 + 70214272 70214272 70214272 TTGGAATAGTATAGTCAGAACAGGTCTAATAGAAAAGGTGACATCTGAGCAAAGACTTAAAGGAG TTGGAATAGTATAGTCAGAACAGGTCTAATAGGAAAGGTGACATCTGAGCAAAGACTTAAAGGAG A G MAMDC2 Ensembl:ENSG00000165072 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:70214226..70214381 26863196 MeRIP-seq:(Medium) rs1301338332 Functional Loss SNV dbSNP153 33..33 33 - - - 60760 RMVar_ID_60760 Human_SNP_ID_401493359 m1A Human chr9 - 70259016 70258993 70259017 CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGCG CCGTTCCCACCGTCCGGCAGCCCAGGCGCCC________________________CGCTCCCGCG GGGGCGCCTGGGTGGATGGGCGCTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70258973..70259143 26863196 MeRIP-seq:(Medium) rs1344863756 Functional Loss DEL dbSNP153 32..55 33 - - - 60761 RMVar_ID_60761 Human_SNP_ID_401493359 m1A Human chr9 - 70259017 70258993 70259017 TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCC________________________CGCTCCCGC GGGGCGCCTGGGTGGATGGGCGCTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70258972..70259151 26863196 MeRIP-seq:(Medium) rs1344863756 Functional Loss DEL dbSNP153 33..56 33 - - - 60762 RMVar_ID_60762 Human_SNP_ID_401493368 m1A Human chr9 - 70259016 70259000 70259016 CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGCG CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCA________________GGCGCCCCGCTCCCGCG CTGGGTGGATGGGCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70258973..70259143 26863196 MeRIP-seq:(Medium) rs1366257797 Functional Loss DEL dbSNP153 33..48 33 - - - 60763 RMVar_ID_60763 Human_SNP_ID_401493384 m1A Human chr9 - 70259016 70259016 70259016 CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGCG CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAGGCGCCCATCCACCCAGGCGCCCCGCTCCCGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70258973..70259143 26863196 MeRIP-seq:(Medium) rs941047795 Functional Loss SNV dbSNP153 33..33 33 - - - 60764 RMVar_ID_60764 Human_SNP_ID_401493385 m1A Human chr9 - 70259017 70259017 70259017 TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCCAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70258972..70259151 26863196 MeRIP-seq:(Medium) rs878983240 Functional Loss SNV dbSNP153 33..33 33 - - - 60765 RMVar_ID_60765 Human_SNP_ID_401493392 m1A Human chr9 - 70259025 70259025 70259025 CAGCGACTTCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCC CAGCGACTTCCGTTCCCACCGTCCGGCAGCCCTGGCGCCCAAGCGCCCATCCACCCAGGCGCCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:70258976..70259138 26863196 MeRIP-seq:(Medium) rs1391567541 Functional Loss SNV dbSNP153 33..33 33 - - - 60766 RMVar_ID_60766 Human_SNP_ID_401531137 m1A Human chr9 + 70413617 70413604 70413617 ACGGCCCCGGGCTCCGCCGCGCCGCCGCCTCTAGCCGCCGCCCCTGCCCCGCGCCGGCCGCGATC ACGGCCCCGGGCTCCGCCGC_____________GCCGCCGCCCCTGCCCCGCGCCGGCCGCGATC CGCCGCCGCCTCTA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70413566..70413686 26863196 MeRIP-seq:(Medium) rs966469874 Functional Loss DEL dbSNP153 21..33 33 - - - 60767 RMVar_ID_60767 Human_SNP_ID_401532731 m1A Human chr9 - 70420042 70420042 70420042 CCGAACCCCTCGCAGGCTTAGCCTGAAGGCAGACGCGGGGCGCAGGTGCTCCCGGGACCGGACCG CCGAACCCCTCGCAGGCTTAGCCTGAAGGCAGCCGCGGGGCGCAGGTGCTCCCGGGACCGGACCG T G lnc-KLF9-5,lnc-KLF9-5:2 RNACentral:URS0000D59DEF,RNACentral:URS0000D57984 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70419991..70420077 26863196 MeRIP-seq:(Medium) rs1165628519 Functional Loss SNV dbSNP153 33..33 33 - - - 60768 RMVar_ID_60768 Human_SNP_ID_401532849 m1A Human chr9 + 70420345 70420345 70420345 AGCAGCTCTCCCCGCGGCCGCGCCCGCCCGGCACCCAGCGCTTCCCGCCGCAGCACACCCCCAAC AGCAGCTCTCCCCGCGGCCGCGCCCGCCCGGCCCCCAGCGCTTCCCGCCGCAGCACACCCCCAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:70420246..70420386;chr9:70420205..70420428 26863196 MeRIP-seq:(Medium) rs914947325 Functional Loss SNV dbSNP153 33..33 33 - - - 60769 RMVar_ID_60769 Human_SNP_ID_401532898 m1A Human chr9 + 70420497 70420497 70420497 GGGTCGAGACGTGTGTAGGTGTAGGGAGGTGGATAGCCCTTTTCCGAGCCGTAGGCGTCACCCCT GGGTCGAGACGTGTGTAGGTGTAGGGAGGTGGCTAGCCCTTTTCCGAGCCGTAGGCGTCACCCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70420447..70420527 26863196 MeRIP-seq:(Medium) rs1021033719 Functional Loss SNV dbSNP153 33..33 33 - - - 60770 RMVar_ID_60770 Human_SNP_ID_401532899 m1A Human chr9 + 70420497 70420497 70420497 GGGTCGAGACGTGTGTAGGTGTAGGGAGGTGGATAGCCCTTTTCCGAGCCGTAGGCGTCACCCCT GGGTCGAGACGTGTGTAGGTGTAGGGAGGTGGGTAGCCCTTTTCCGAGCCGTAGGCGTCACCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70420447..70420527 26863196 MeRIP-seq:(Medium) rs1021033719 Functional Loss SNV dbSNP153 33..33 33 - - - 60771 RMVar_ID_60771 Human_SNP_ID_401532969 m1A Human chr9 - 70420814 70420814 70420814 TATGTGTGGAAATGAAACTGGGAGGAGGAGGGAGAGAGGGAAGAGCGGGCACGCACTTCTCGGCT TATGTGTGGAAATGAAACTGGGAGGAGGAGGGCGAGAGGGAAGAGCGGGCACGCACTTCTCGGCT T G lnc-KLF9-5 RNACentral:URS0000D59DEF lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70420763..70420875 26863196 MeRIP-seq:(Medium) rs1298000149 Functional Loss SNV dbSNP153 33..33 33 - - - 60772 RMVar_ID_60772 Human_SNP_ID_401774143 m1A Human chr9 + 71420738 71420735 71420738 AGAAAGAAAGAGAGAAAGAGAGAGAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGA AGAAAGAAAGAGAGAAAGAGAGAGAGAGAG___GAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGA GAAA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:71420713..71420800 26863410 MeRIP-seq:(Medium) rs1565557112 Functional Loss DEL dbSNP153 31..33 33 - - - 60773 RMVar_ID_60773 Human_SNP_ID_401774149 m1A Human chr9 + 71420738 71420738 71420738 AGAAAGAAAGAGAGAAAGAGAGAGAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGA AGAAAGAAAGAGAGAAAGAGAGAGAGAGAGAAGGAGAGAGAAAGAGAGAGAAAGAGAGAGAAAGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:71420713..71420800 26863410 MeRIP-seq:(Medium) rs1442862013 Functional Loss SNV dbSNP153 33..33 33 - - - 60774 RMVar_ID_60774 Human_SNP_ID_401837311 m1A Human chr9 + 71683870 71683870 71683870 CAGTGTCAGCCTGAACACACTTTCTACCACCCACCCTTGGCCATCCCTCCTCTACACTTTATGCG CAGTGTCAGCCTGAACACACTTTCTACCACCCCCCCTTGGCCATCCCTCCTCTACACTTTATGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:71683767..71683976 26863196 MeRIP-seq:(Medium) rs192920734 Functional Loss SNV dbSNP153 33..33 33 - - - 60775 RMVar_ID_60775 Human_SNP_ID_401837507 m1A Human chr9 + 71684702 71684702 71684702 GGGCCTGAGTTGCCACTTAAAACTGTCATTCAATATCATAGAAAATCCTCAAAGGCTGCCCAGAA GGGCCTGAGTTGCCACTTAAAACTGTCATTCAGTATCATAGAAAATCCTCAAAGGCTGCCCAGAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:71684656..71684825 26863196 MeRIP-seq:(Medium) rs192841672 Functional Loss SNV dbSNP153 33..33 33 - - - 60776 RMVar_ID_60776 Human_SNP_ID_401875674 m1A Human chr9 - 71835774 71835771 71835775 AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGAAAGAGGAAAAGAAAAAGAGAAAGGAAGAAGGAAG AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGA____GGAAAAGAAAAAGAGAAAGGAAGAAGGAAG CTCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:71835725..71835809 26863196 MeRIP-seq:(Medium) rs553452074 Functional Loss DEL dbSNP153 32..35 33 - - - 60777 RMVar_ID_60777 Human_SNP_ID_401875675 m1A Human chr9 - 71835774 71835773 71835775 AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGAAAGAGGAAAAGAAAAAGAGAAAGGAAGAAGGAAG AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGA__GAGGAAAAGAAAAAGAGAAAGGAAGAAGGAAG CTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:71835725..71835809 26863196 MeRIP-seq:(Medium) rs1470789908 Functional Loss DEL dbSNP153 32..33 33 - - - 60778 RMVar_ID_60778 Human_SNP_ID_401875676 m1A Human chr9 - 71835774 71835774 71835774 AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGAAAGAGGAAAAGAAAAAGAGAAAGGAAGAAGGAAG AAGAAGAAAGAAAGAAAAAGAAAAAGAAAGAAGGAGGAAAAGAAAAAGAGAAAGGAAGAAGGAAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:71835725..71835809 26863196 MeRIP-seq:(Medium) rs1045195223 Functional Loss SNV dbSNP153 33..33 33 - - - 60779 RMVar_ID_60779 Human_SNP_ID_401891518 m1A Human chr9 - 71901677 71901671 71901678 AGGGGGATGGGGAAAGAGTGAAATGCAGGTGGAGATATTTCAGAGTCTAGAGTTTAAGGGGAGAG AGGGGGATGGGGAAAGAGTGAAATGCAGGTG_______TTCAGAGTCTAGAGTTTAAGGGGAGAG AATATCTC A ABHD17B Ensembl:ENSG00000107362 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:71901676..71901799 26863196 MeRIP-seq:(Medium) rs923304734 Functional Loss DEL dbSNP153 32..38 33 - - - 60780 RMVar_ID_60780 Human_SNP_ID_401951158 m1A Human chr9 + 72149487 72149486 72149488 CCTGTGTCCGCCCGGCAGCCGCCCGCAGCTGCAGAGAGTCCCGCTGCGTCTCCGCCGCGTGCGCC CCTGTGTCCGCCCGGCAGCCGCCCGCAGCTGC__AGAGTCCCGCTGCGTCTCCGCCGCGTGCGCC CAG C GDA Ensembl:ENSG00000119125 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:72149387..72149650 26863196 MeRIP-seq:(Medium) rs1016210503 Functional Loss DEL dbSNP153 33..34 33 - - - 60781 RMVar_ID_60781 Human_SNP_ID_401954347 m1A Human chr9 + 72163069 72163063 72163069 GGAAGAGATGAGTTAGAAAATGACTGCAGTGGACCACAAAAGAGACAGGTAGATGGTGATAGACA GGAAGAGATGAGTTAGAAAATGACTGC______CCACAAAAGAGACAGGTAGATGGTGATAGACA CAGTGGA C GDA Ensembl:ENSG00000119125 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:72163063..72163187 26863196 MeRIP-seq:(Medium) rs1033648821 Functional Loss DEL dbSNP153 28..33 33 - - - 60782 RMVar_ID_60782 Human_SNP_ID_401954349 m1A Human chr9 + 72163069 72163069 72163069 GGAAGAGATGAGTTAGAAAATGACTGCAGTGGACCACAAAAGAGACAGGTAGATGGTGATAGACA GGAAGAGATGAGTTAGAAAATGACTGCAGTGGGCCACAAAAGAGACAGGTAGATGGTGATAGACA A G GDA Ensembl:ENSG00000119125 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:72163063..72163187 26863196 MeRIP-seq:(Medium) rs1047545725 Functional Loss SNV dbSNP153 33..33 33 - - - 60783 RMVar_ID_60783 Human_SNP_ID_401954590 m1A Human chr9 + 72164184 72164184 72164184 TATCTGAACGGGCGATATAAAATGTAGAGTAAAGGTTGAGAAGACAACAGGAACTAGACTAATTC TATCTGAACGGGCGATATAAAATGTAGAGTAAGGGTTGAGAAGACAACAGGAACTAGACTAATTC A G GDA Ensembl:ENSG00000119125 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:72164181..72164466 26863196 MeRIP-seq:(Medium) rs542016529 Functional Loss SNV dbSNP153 33..33 33 - - - 60784 RMVar_ID_60784 Human_SNP_ID_402002194 m1A Human chr9 + 72364658 72364658 72364658 GTCCCTTCACTCCCGCCCCCGGCCCGGCAACAAGGAGCCCGGCTCCCACCCGCAGCCCCGTATCA GTCCCTTCACTCCCGCCCCCGGCCCGGCAACATGGAGCCCGGCTCCCACCCGCAGCCCCGTATCA A T RF00017-4503,RF00017-4596,RF00017-4672 RNACentral:URS0000948B80,RNACentral:URS0000934741,RNACentral:URS00009A3B2E SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:72364657..72364788 32194978 MeRIP-seq:(Medium) rs1411516790 Functional Loss SNV dbSNP153 33..33 33 - - - 60785 RMVar_ID_60785 Human_SNP_ID_402002279 m1A Human chr9 + 72364823 72364823 72364823 GGTGCCGCCGCCGCGGGCCGGGAGCGGGTCGGAGCAGCAGGCGGAGGTGGCGCCGCCGCCGCCGC GGTGCCGCCGCCGCGGGCCGGGAGCGGGTCGGCGCAGCAGGCGGAGGTGGCGCCGCCGCCGCCGC A C RF00017-4503,RF00017-4596,RF00017-4672 RNACentral:URS0000948B80,RNACentral:URS0000934741,RNACentral:URS00009A3B2E SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr9:72364508..72365191;chr9:72364705..72365175 26863196 MeRIP-seq:(Medium) rs988868333 Functional Loss SNV dbSNP153 33..33 33 - - - 60786 RMVar_ID_60786 Human_SNP_ID_402002335 m1A Human chr9 + 72364946 72364944 72364947 GGAAGTGGGAGGAGGGAAGCGAGGGGGGGCCGAGGAGGAGGTGGAGGGAGGACCGGCGGCCGCAG GGAAGTGGGAGGAGGGAAGCGAGGGGGGGCC___GAGGAGGTGGAGGGAGGACCGGCGGCCGCAG CGAG C RF00017-4503,RF00017-4596,RF00017-4672 RNACentral:URS0000948B80,RNACentral:URS0000934741,RNACentral:URS00009A3B2E SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:72364676..72365200 26863196 MeRIP-seq:(Medium) rs1237488803 Functional Loss DEL dbSNP153 32..34 33 - - - 60787 RMVar_ID_60787 Human_SNP_ID_402002356 m1A Human chr9 + 72364985 72364985 72364985 GGTGGAGGGAGGACCGGCGGCCGCAGCGGCTAACGCTGCTCGAGGCGCTCGCCTGTCGTCGCCTC GGTGGAGGGAGGACCGGCGGCCGCAGCGGCTATCGCTGCTCGAGGCGCTCGCCTGTCGTCGCCTC A T RF00017-4503,RF00017-4596,RF00017-4672 RNACentral:URS0000948B80,RNACentral:URS0000934741,RNACentral:URS00009A3B2E SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:72364701..72365164 26863410 MeRIP-seq:(Medium) rs973962726 Functional Loss SNV dbSNP153 33..33 33 - - - 60788 RMVar_ID_60788 Human_SNP_ID_402192433 m1A Human chr9 + 73159389 73159389 73159389 TCTAACTAAGCGAAACAATGCACAGCGTCAACAGATCAAAGCAGCATATCTCCAGGAAACAGGAA TCTAACTAAGCGAAACAATGCACAGCGTCAACGGATCAAAGCAGCATATCTCCAGGAAACAGGAA A G ANXA1 Ensembl:ENSG00000135046 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:73158526..73159446 32194978 MeRIP-seq:(Medium) rs757802790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91002,Human_RBP_ID_17322868,Human_RBP_ID_22466104 Human_Splice_Rec_1052856,Human_Splice_Rec_1052864,Human_Splice_Rec_1052865,Human_Splice_Rec_1052878,Human_Splice_Rec_1052879,Human_Splice_Rec_1052904,Human_Splice_Rec_1052905,Human_Splice_Rec_1052910,Human_Splice_Rec_1052911 Human_miRNA_ID_1984614 RMVar_hsa_circ_58215,RMVar_hsa_circ_115712,RMVar_hsa_circ_119809,RMVar_hsa_circ_257161,RMVar_hsa_circ_257162,RMVar_hsa_circ_27860,RMVar_hsa_circ_353156 60789 RMVar_ID_60789 Human_SNP_ID_402627990 m1A Human chr9 - 74948104 74948104 74948104 CAGACATTGAAGATTTAAGTGAAGACACCCTGACAGAAGCAACACTTCAGGGCAGGAATGAAGGG CAGACATTGAAGATTTAAGTGAAGACACCCTGTCAGAAGCAACACTTCAGGGCAGGAATGAAGGG T A C9orf40 Ensembl:ENSG00000135045 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:74948053..74948151 26863196 MeRIP-seq:(Medium) rs1300118699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1705865,Human_RBP_ID_2065354,Human_RBP_ID_8706129,Human_RBP_ID_16697475,Human_RBP_ID_24306745 Human_miRNA_ID_2452176 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 60790 RMVar_ID_60790 Human_SNP_ID_402628947 m1A Human chr9 - 74952244 74952244 74952244 CCCGGGCGCCCGGCTCCCGGGGGGCGGTGGCGACGACGGGGCGGGGCGCGCAGGACCCCCGCGGG CCCGGGCGCCCGGCTCCCGGGGGGCGGTGGCGGCGACGGGGCGGGGCGCGCAGGACCCCCGCGGG T C C9orf40 Ensembl:ENSG00000135045 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr9:74948164..74952391;chr9:74952242..74952342 26863410 MeRIP-seq:(Medium) rs1373436144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036804 Human_Splice_Rec_1053269 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 60791 RMVar_ID_60791 Human_SNP_ID_402628999 m1A Human chr9 - 74952330 74952328 74952330 GGCCAGGAGCGTGAGGACCACGGTCTGGAGACAGGCGATCCGCCGCTGCCGCCGCCGCCCGTACT GGCCAGGAGCGTGAGGACCACGGTCTGGAGAC__GCGATCCGCCGCTGCCGCCGCCGCCCGTACT CCT C C9orf40 Ensembl:ENSG00000135045 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:74952242..74952400 26863196 MeRIP-seq:(Medium) rs781393935 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9338923 Human_miRNA_ID_2225240 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 60792 RMVar_ID_60792 Human_SNP_ID_402629001 m1A Human chr9 - 74952330 74952330 74952330 GGCCAGGAGCGTGAGGACCACGGTCTGGAGACAGGCGATCCGCCGCTGCCGCCGCCGCCCGTACT GGCCAGGAGCGTGAGGACCACGGTCTGGAGACGGGCGATCCGCCGCTGCCGCCGCCGCCCGTACT T C C9orf40 Ensembl:ENSG00000135045 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:74952242..74952400 26863196 MeRIP-seq:(Medium) rs777991430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338923 Human_miRNA_ID_2225240 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 60793 RMVar_ID_60793 Human_SNP_ID_402629172 m1A Human chr9 + 74952772 74952772 74952772 CGCTGGAGGGGGTAGGGCGGGGCAGCTCGCGCAGGGCCTAGGGCTGGGGCTCCGGCTCGGAGGCA CGCTGGAGGGGGTAGGGCGGGGCAGCTCGCGCTGGGCCTAGGGCTGGGGCTCCGGCTCGGAGGCA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:74952476..74952875 26863410 MeRIP-seq:(Medium) rs1205571141 Functional Loss SNV dbSNP153 33..33 33 - - - 60794 RMVar_ID_60794 Human_SNP_ID_402629175 m1A Human chr9 - 74952784 74952784 74952784 GAGCGCGGGAGCTGCCTCCGAGCCGGAGCCCCAGCCCTAGGCCCTGCGCGAGCTGCCCCGCCCTA GAGCGCGGGAGCTGCCTCCGAGCCGGAGCCCCCGCCCTAGGCCCTGCGCGAGCTGCCCCGCCCTA T G C9orf40 Ensembl:ENSG00000135045 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:74952685..74952886 26863410 MeRIP-seq:(Medium) rs1465059431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1339418,Human_RBP_ID_1403513,Human_RBP_ID_5035719,Human_RBP_ID_9339460,Human_RBP_ID_22341072 Human_miRNA_ID_2573172,Human_miRNA_ID_2684314 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 60795 RMVar_ID_60795 Human_SNP_ID_564698825 m1A Human chr14 + 90256577 90256577 90256577 GCCGCAGTGGTGGAGGAACTTCCGGCAGCGGCAGCTCAAGTGGCCAAGGCAAGATGGTGAGTGAC GCCGCAGTGGTGGAGGAACTTCCGGCAGCGGCGGCTCAAGTGGCCAAGGCAAGATGGTGAGTGAC A G PSMC1 Ensembl:ENSG00000100764 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:90256551..90256668 26863196 MeRIP-seq:(Medium) rs199718567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758215 Human_Splice_Rec_1544405,Human_Splice_Rec_1544411,Human_Splice_Rec_1544431,Human_Splice_Rec_1544439,Human_Splice_Rec_1544447 60796 RMVar_ID_60796 Human_SNP_ID_564699467 m1A Human chr14 - 90259152 90259150 90259153 CATGACCACCACTCTGACTTTGACCCTGGAGGAGAAAAATCAGGCACAGATGTAAATTCAGAATA CATGACCACCACTCTGACTTTGACCCTGGAG___AAAAATCAGGCACAGATGTAAATTCAGAATA TCTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:90259151..90259200 26863196 MeRIP-seq:(Medium) rs1247428035 Functional Loss DEL dbSNP153 32..34 33 - - - 60797 RMVar_ID_60797 Human_SNP_ID_564734078 m1A Human chr14 + 90397112 90397112 90397112 CGGCGGCGCAGGCGGCGGCGGCGGCATAGCGCACAGCGCGCCTTAGCAGCAGCAGCAGCAGCAGC CGGCGGCGCAGGCGGCGGCGGCGGCATAGCGCGCAGCGCGCCTTAGCAGCAGCAGCAGCAGCAGC A G CALM1 Ensembl:ENSG00000198668 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:90397051..90397125 26863196 MeRIP-seq:(Medium) rs1482315950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1500684,Human_RBP_ID_4304680,Human_RBP_ID_5112742,Human_RBP_ID_5463803,Human_RBP_ID_9369287,Human_RBP_ID_22438809,Human_RBP_ID_26808165 Human_Splice_Rec_1544613 Human_miRNA_ID_325387 60798 RMVar_ID_60798 Human_SNP_ID_564734082 m1A Human chr14 - 90397122 90397122 90397122 CTCCGATGCCGCTGCTGCTGCTGCTGCTGCTAAGGCGCGCTGTGCGCTATGCCGCCGCCGCCGCC CTCCGATGCCGCTGCTGCTGCTGCTGCTGCTACGGCGCGCTGTGCGCTATGCCGCCGCCGCCGCC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:90397058..90397156 26863410 MeRIP-seq:(Medium) rs907168970 Functional Loss SNV dbSNP153 33..33 33 - - - 60799 RMVar_ID_60799 Human_SNP_ID_564734145 m1A Human chr14 + 90397228 90397228 90397228 TCGCTCCCTCTGCTCTTCCTCCCTTCGCTCGCACCATGGTAGGTCGGGAGTGGCAAATGCCGGCG TCGCTCCCTCTGCTCTTCCTCCCTTCGCTCGCGCCATGGTAGGTCGGGAGTGGCAAATGCCGGCG A G CALM1 Ensembl:ENSG00000198668 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:90397201..90397250 26863196 MeRIP-seq:(Medium) rs1566721983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308460,Human_RBP_ID_5418375,Human_RBP_ID_5463629,Human_RBP_ID_19064263 Human_Splice_Rec_1544563,Human_Splice_Rec_1544575,Human_Splice_Rec_1544585,Human_Splice_Rec_1544587,Human_Splice_Rec_1544589,Human_Splice_Rec_1544593,Human_Splice_Rec_1544599,Human_Splice_Rec_1544605 60800 RMVar_ID_60800 Human_SNP_ID_564734586 m1A Human chr14 + 90398176 90398176 90398176 TGGCGCGCGGCTTGGTTTCCATTAGAGACGCAAAGTTTCTGCTCCGGGAGGAGGCGGCGGCGCCG TGGCGCGCGGCTTGGTTTCCATTAGAGACGCATAGTTTCTGCTCCGGGAGGAGGCGGCGGCGCCG A T CALM1 Ensembl:ENSG00000198668 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:90398173..90398373 26863196 MeRIP-seq:(Medium) rs1214946956 Functional Loss SNV dbSNP153 33..33 33 - - - 60801 RMVar_ID_60801 Human_SNP_ID_564735394 m1A Human chr14 + 90401227 90401227 90401227 AAGTGTGTATTGTGACTGGGTTGGATAAAGACATTGATTCTAACGGGTCAACTTTTGTTTTCAGA AAGTGTGTATTGTGACTGGGTTGGATAAAGACGTTGATTCTAACGGGTCAACTTTTGTTTTCAGA A G CALM1 Ensembl:ENSG00000198668 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:90401225..90401328 26863196 MeRIP-seq:(Medium) rs766745492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22540056 60802 RMVar_ID_60802 Human_SNP_ID_564735398 m1A Human chr14 - 90401235 90401235 90401235 CCTTGAATTCTGAAAACAAAAGTTGACCCGTTAGAATCAATGTCTTTATCCAACCCAGTCACAAT CCTTGAATTCTGAAAACAAAAGTTGACCCGTTGGAATCAATGTCTTTATCCAACCCAGTCACAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:90401233..90401332 26863196 MeRIP-seq:(Medium) rs1046712559 Functional Loss SNV dbSNP153 33..33 33 - - - 60803 RMVar_ID_60803 Human_SNP_ID_564736559 m1A Human chr14 + 90405764 90405763 90405765 CAACCTCTGAGCCCAAGACCTTGCCTGAAAACAAGCAGATACCGATTGCTTCATCCTATTTATGG CAACCTCTGAGCCCAAGACCTTGCCTGAAAAC__GCAGATACCGATTGCTTCATCCTATTTATGG CAA C CALM1 Ensembl:ENSG00000198668 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:90405725..90405826 32194978 MeRIP-seq:(Medium) rs977738212 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_453400,Human_RBP_ID_1500747,Human_RBP_ID_9047247,Human_RBP_ID_12441024,Human_RBP_ID_17248164 60804 RMVar_ID_60804 Human_SNP_ID_564779438 m1A Human chr14 + 90573340 90573340 90573340 ACTGCTGTCCCGATGCTCTTTCCATGGTTCTCAGTGCATGGTCCCTCTCCGGCTCACGGTCCCTC ACTGCTGTCCCGATGCTCTTTCCATGGTTCTCGGTGCATGGTCCCTCTCCGGCTCACGGTCCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:90573335..90573867 26863196 MeRIP-seq:(Medium) rs573982072 Functional Loss SNV dbSNP153 33..33 33 - - - 60805 RMVar_ID_60805 Human_SNP_ID_564779888 m1A Human chr14 + 90574746 90574746 90574746 CTGTTCTCTGCCGTCACATCAGCCACCTGACCACCACCTGTGACACAGACAATGAGGCTTCCTTC CTGTTCTCTGCCGTCACATCAGCCACCTGACCGCCACCTGTGACACAGACAATGAGGCTTCCTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:90574744..90575039 26863196 MeRIP-seq:(Medium) rs189912338 Functional Loss SNV dbSNP153 33..33 33 - - - 60806 RMVar_ID_60806 Human_SNP_ID_564779961 m1A Human chr14 - 90575046 90575046 90575046 CTGTGTGGCGGAGAGTGGCGGAAACAGAGCTGAGCGTTGACAGTTGCCTGGCACACAGGGAGAGC CTGTGTGGCGGAGAGTGGCGGAAACAGAGCTGGGCGTTGACAGTTGCCTGGCACACAGGGAGAGC T C TTC7B Ensembl:ENSG00000165914 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:90574946..90575094 26863196 MeRIP-seq:(Medium) rs561777362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168504,RMVar_hsa_circ_90909 60807 RMVar_ID_60807 Human_SNP_ID_564824583 m1A Human chr14 + 90767029 90767027 90767029 GGCCTTGTCTGTTAATAAATAGTTTATATACCAAAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA GGCCTTGTCTGTTAATAAATAGTTTATATAC__AAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA CCA C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1491463493 Functional Loss DEL dbSNP153 32..33 33 - - - 60808 RMVar_ID_60808 Human_SNP_ID_564824597 m1A Human chr14 + 90767029 90767029 90767029 GGCCTTGTCTGTTAATAAATAGTTTATATACCAAAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA GGCCTTGTCTGTTAATAAATAGTTTATATACCCAAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1460426505 Functional Loss SNV dbSNP153 33..33 33 - - - 60809 RMVar_ID_60809 Human_SNP_ID_564824598 m1A Human chr14 + 90767029 90767029 90767029 GGCCTTGTCTGTTAATAAATAGTTTATATACCAAAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA GGCCTTGTCTGTTAATAAATAGTTTATATACCGAAAAAAAAAAAAAAAAGAAAGAAAGGAAGAAA A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1460426505 Functional Loss SNV dbSNP153 33..33 33 - - - 60810 RMVar_ID_60810 Human_SNP_ID_564836381 m1A Human chr14 + 90816336 90816336 90816336 GGCCGGGCCCGGCCGCCCGCCCCGCAGGCCCCACCGCCGCCGCCGCGGCGCCCCCTCGCCGCCTC GGCCGGGCCCGGCCGCCCGCCCCGCAGGCCCCGCCGCCGCCGCCGCGGCGCCCCCTCGCCGCCTC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr14:90816275..90816400 26863410 MeRIP-seq:(Medium) rs1353961218 Functional Loss SNV dbSNP153 33..33 33 - - - 60811 RMVar_ID_60811 Human_SNP_ID_564853055 m1A Human chr14 - 90883331 90883331 90883331 ACAATTAAAATTATTGAGTGTGAGGAACAGAGAGAAAAATGAAAAAAAGCGAACAGAGCCTAAGG ACAATTAAAATTATTGAGTGTGAGGAACAGAGTGAAAAATGAAAAAAAGCGAACAGAGCCTAAGG T A RPS6KA5 Ensembl:ENSG00000100784 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:90883284..90883410 26863196 MeRIP-seq:(Medium) rs1029749553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5309,RMVar_hsa_circ_60311,RMVar_hsa_circ_291165,RMVar_hsa_circ_318699,RMVar_hsa_circ_351395,RMVar_hsa_circ_267250,RMVar_hsa_circ_28365,RMVar_hsa_circ_168541,RMVar_hsa_circ_168542,RMVar_hsa_circ_3430 60812 RMVar_ID_60812 Human_SNP_ID_564853056 m1A Human chr14 - 90883331 90883331 90883331 ACAATTAAAATTATTGAGTGTGAGGAACAGAGAGAAAAATGAAAAAAAGCGAACAGAGCCTAAGG ACAATTAAAATTATTGAGTGTGAGGAACAGAGGGAAAAATGAAAAAAAGCGAACAGAGCCTAAGG T C RPS6KA5 Ensembl:ENSG00000100784 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:90883284..90883410 26863196 MeRIP-seq:(Medium) rs1029749553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5309,RMVar_hsa_circ_60311,RMVar_hsa_circ_291165,RMVar_hsa_circ_318699,RMVar_hsa_circ_351395,RMVar_hsa_circ_267250,RMVar_hsa_circ_28365,RMVar_hsa_circ_168541,RMVar_hsa_circ_168542,RMVar_hsa_circ_3430 60813 RMVar_ID_60813 Human_SNP_ID_564864951 m1A Human chr14 + 90933819 90933815 90933819 CCATGTCCTTCTTTCCTACTACTGTAACTCTCACTCATTCTGTATGCCCACAACGGCCTCTAACC CCATGTCCTTCTTTCCTACTACTGTAACT____CTCATTCTGTATGCCCACAACGGCCTCTAACC TCTCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:90933791..90933991 26863196 MeRIP-seq:(Medium) rs1450542191 Functional Loss DEL dbSNP153 30..33 33 - - - 60814 RMVar_ID_60814 Human_SNP_ID_564873548 m1A Human chr14 + 90969957 90969957 90969957 CCTTCTGATATGCTTCACTTCCATGAACTCCCATACCTCCTGTTCTCATTTCTACCTACTCTTTC CCTTCTGATATGCTTCACTTCCATGAACTCCCGTACCTCCTGTTCTCATTTCTACCTACTCTTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:90969896..90969991 26863196 MeRIP-seq:(Medium) rs1328166388 Functional Loss SNV dbSNP153 33..33 33 - - - 60815 RMVar_ID_60815 Human_SNP_ID_564881197 m1A Human chr14 - 91001161 91001161 91001161 CTCTTGTTTTTTTTTTCCTCTTTTTTTCTTTTAGCTAATTTGACAGGACATGCTGAGAAGGTGGG CTCTTGTTTTTTTTTTCCTCTTTTTTTCTTTTTGCTAATTTGACAGGACATGCTGAGAAGGTGGG T A RPS6KA5 Ensembl:ENSG00000100784 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:91001139..91001214 26863196 MeRIP-seq:(Medium) rs1201492111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944625,Human_RBP_ID_6394673 Human_Splice_Rec_1544983,Human_Splice_Rec_1545015,Human_Splice_Rec_1545051,Human_Splice_Rec_1545109,Human_Splice_Rec_1545133,Human_Splice_Rec_1545155 RMVar_hsa_circ_100401,RMVar_hsa_circ_90803,RMVar_hsa_circ_168554,RMVar_hsa_circ_168555,RMVar_hsa_circ_168565,RMVar_hsa_circ_168562,RMVar_hsa_circ_168566 60816 RMVar_ID_60816 Human_SNP_ID_564895738 m1A Human chr14 - 91060424 91060424 91060424 GGGATCGGAAAAAAAGGAGAAGATGGAGGAGGAGGGTGGCAGCAGCGGCGGCGCCGCGGGGACCA GGGATCGGAAAAAAAGGAGAAGATGGAGGAGGCGGGTGGCAGCAGCGGCGGCGCCGCGGGGACCA T G RPS6KA5 Ensembl:ENSG00000100784 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:91060377..91060576 26863196 MeRIP-seq:(Medium) rs1274552217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26325996 Human_Splice_Rec_1544981,Human_Splice_Rec_1545013,Human_Splice_Rec_1545107,Human_Splice_Rec_1545131,Human_Splice_Rec_1545151 RMVar_hsa_circ_100401,RMVar_hsa_circ_168554 60817 RMVar_ID_60817 Human_SNP_ID_564895763 m1A Human chr14 + 91060480 91060480 91060480 TCCGATCCCGCGGGTCGCTACGAGGGGAACCCAGGAGACAGCGGACGCCCGTCCCCTCGCAGCCG TCCGATCCCGCGGGTCGCTACGAGGGGAACCCCGGAGACAGCGGACGCCCGTCCCCTCGCAGCCG A C DGLUCY Ensembl:ENSG00000133943 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:91060430..91060572 26863196 MeRIP-seq:(Medium) rs1482643187 Functional Loss SNV dbSNP153 33..33 33 - - - 60818 RMVar_ID_60818 Human_SNP_ID_564895789 m1A Human chr14 - 91060554 91060554 91060554 CAGAGCGGGAAAGAGACTCGTCTTTGCGTCCGAGTTCTGGAGCCGCCGCACCCCGACTCCTGGGG CAGAGCGGGAAAGAGACTCGTCTTTGCGTCCGTGTTCTGGAGCCGCCGCACCCCGACTCCTGGGG T A RPS6KA5 Ensembl:ENSG00000100784 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91060504..91060646 26863196 MeRIP-seq:(Medium) rs1319767547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100401,RMVar_hsa_circ_168554 60819 RMVar_ID_60819 Human_SNP_ID_564950727 m1A Human chr14 - 91272352 91272352 91272352 ACAAATAATCCACGTCAGCATGGGGACCAATTAGGATGCAATGACAAACTGACTTCCCCCAAAGC ACAAATAATCCACGTCAGCATGGGGACCAATTTGGATGCAATGACAAACTGACTTCCCCCAAAGC T A CCDC88C Ensembl:ENSG00000015133 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12878426 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7358 RMVar_hsa_circ_268120 60820 RMVar_ID_60820 Human_SNP_ID_564950728 m1A Human chr14 - 91272352 91272352 91272352 ACAAATAATCCACGTCAGCATGGGGACCAATTAGGATGCAATGACAAACTGACTTCCCCCAAAGC ACAAATAATCCACGTCAGCATGGGGACCAATTCGGATGCAATGACAAACTGACTTCCCCCAAAGC T G CCDC88C Ensembl:ENSG00000015133 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12878426 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7358 RMVar_hsa_circ_268120 60821 RMVar_ID_60821 Human_SNP_ID_564956195 m1A Human chr14 - 91291032 91291032 91291032 GAAGACATAAGGAAAAGCTGGAAGAAAAAATCATGGATCAATACAAGTTCTATGATCCTCCTCCA GAAGACATAAGGAAAAGCTGGAAGAAAAAATCGTGGATCAATACAAGTTCTATGATCCTCCTCCA T C CCDC88C Ensembl:ENSG00000015133 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:91290993..91291078 26863410 MeRIP-seq:(Medium) rs773778383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545764,Human_Splice_Rec_1545765,Human_Splice_Rec_1545799 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60822 RMVar_ID_60822 Human_SNP_ID_564956770 m1A Human chr14 - 91293057 91293057 91293057 ACAGGAAGGTGGGCTGTGGCAGGTGAGGGGACAGGAAGGTCAGCCGTGGCAGGTGAGGACGGGAA ACAGGAAGGTGGGCTGTGGCAGGTGAGGGGACGGGAAGGTCAGCCGTGGCAGGTGAGGACGGGAA T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:91292998..91293199 26863196 MeRIP-seq:(Medium) rs1319475328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8180967 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60823 RMVar_ID_60823 Human_SNP_ID_564956825 m1A Human chr14 - 91293158 91293130 91293158 AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTATGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCT____________________________GTGGC CAGCCCACCTTCCCATCCTCACCTGCCAT C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293123..91293251 26863196 MeRIP-seq:(Medium) rs1567054648 Functional Loss DEL dbSNP153 33..60 33 - - - RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60824 RMVar_ID_60824 Human_SNP_ID_564956843 m1A Human chr14 - 91293158 91293158 91293158 AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTATGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTTTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC T A CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293123..91293251 26863196 MeRIP-seq:(Medium) rs77218441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60825 RMVar_ID_60825 Human_SNP_ID_564956844 m1A Human chr14 - 91293158 91293158 91293158 AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTATGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293123..91293251 26863196 MeRIP-seq:(Medium) rs77218441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60826 RMVar_ID_60826 Human_SNP_ID_564956845 m1A Human chr14 - 91293158 91293158 91293158 AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTATGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTCTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC T G CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293123..91293251 26863196 MeRIP-seq:(Medium) rs77218441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60827 RMVar_ID_60827 Human_SNP_ID_564956953 m1A Human chr14 - 91293299 91293299 91293299 TGGCAGGTGAGGATGGGAAGGTGGGCCGTGGCAGGTGAGGGGACAGGAAGGTCGGCCGTGGCAGG TGGCAGGTGAGGATGGGAAGGTGGGCCGTGGCGGGTGAGGGGACAGGAAGGTCGGCCGTGGCAGG T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:91293255..91293339 26863196 MeRIP-seq:(Medium) rs753541731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60828 RMVar_ID_60828 Human_SNP_ID_564957106 m1A Human chr14 - 91293465 91293434 91293465 GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTGAGGACGGG GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGG_______________________________GG CCGTCCTCACCTGCCACGGTCCACCTTCCCAT C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293445..91293518 26863196 MeRIP-seq:(Medium) rs1567055309 Functional Loss DEL dbSNP153 33..63 33 - - - Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60829 RMVar_ID_60829 Human_SNP_ID_564957115 m1A Human chr14 - 91293465 91293439 91293465 GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTGAGGACGGG GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGG__________________________GGACGGG CTCACCTGCCACGGTCCACCTTCCCAT C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293445..91293518 26863196 MeRIP-seq:(Medium) rs1567055328 Functional Loss DEL dbSNP153 33..58 33 - - - Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60830 RMVar_ID_60830 Human_SNP_ID_564957125 m1A Human chr14 - 91293465 91293450 91293465 GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTGAGGACGGG GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGG_______________GTGGCAGGTGAGGACGGG CGGTCCACCTTCCCAT C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293445..91293518 26863196 MeRIP-seq:(Medium) rs1567055375 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60831 RMVar_ID_60831 Human_SNP_ID_564957146 m1A Human chr14 - 91293465 91293465 91293465 GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTGAGGACGGG GAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGGTGGGAAGGTGGACCGTGGCAGGTGAGGACGGG T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293445..91293518 26863196 MeRIP-seq:(Medium) rs867589963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60832 RMVar_ID_60832 Human_SNP_ID_564957154 m1A Human chr14 - 91293473 91293473 91293473 TGGCAGGTGAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTG TGGCAGGTGAGGATGGGAAGGTGAGCTGTGGCGGGTGAGGATGGGAAGGTGGACCGTGGCAGGTG T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:91292955..91293583;chr14:91292946..91293621;chr14:91293411..91293538 26863196 MeRIP-seq:(Medium) rs61988373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 60833 RMVar_ID_60833 Human_SNP_ID_564963018 m1A Human chr14 - 91313322 91313319 91313322 AGGCCCTGGAGCAGGAGGTGGCCCAGCTCGAGAAGGATAAGAAGCTGCTGGAGAAGGAGGCCAAG AGGCCCTGGAGCAGGAGGTGGCCCAGCTCGAG___GATAAGAAGCTGCTGGAGAAGGAGGCCAAG CCTT C CCDC88C Ensembl:ENSG00000015133 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:91313274..91313358 26863196 MeRIP-seq:(Medium) rs1567069158 Functional Loss DEL dbSNP153 33..35 33 - - - Human_miRNA_ID_2790985 RMVar_hsa_circ_268120,RMVar_hsa_circ_49370,RMVar_hsa_circ_80740,RMVar_hsa_circ_168583,RMVar_hsa_circ_3066,RMVar_hsa_circ_168585,RMVar_hsa_circ_375984,RMVar_hsa_circ_97683,RMVar_hsa_circ_168584 60834 RMVar_ID_60834 Human_SNP_ID_564963299 m1A Human chr14 - 91313913 91313913 91313913 AGGAGAAGGGGGAGCGGGCAGAGAAGCTGGAGAGGGAGCTACAGCGACTCCAGGAGGAGAACGGG AGGAGAAGGGGGAGCGGGCAGAGAAGCTGGAGGGGGAGCTACAGCGACTCCAGGAGGAGAACGGG T C CCDC88C Ensembl:ENSG00000015133 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:91313862..91314099 26863196 MeRIP-seq:(Medium) rs1192030234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812694,Human_RBP_ID_880627,Human_RBP_ID_3945064,Human_RBP_ID_9369301,Human_RBP_ID_18980938,Human_RBP_ID_26325324,Human_RBP_ID_27809092 RMVar_hsa_circ_268120,RMVar_hsa_circ_49370,RMVar_hsa_circ_80740,RMVar_hsa_circ_168583,RMVar_hsa_circ_3066,RMVar_hsa_circ_168585,RMVar_hsa_circ_375984,RMVar_hsa_circ_97683,RMVar_hsa_circ_168584 60835 RMVar_ID_60835 Human_SNP_ID_564985717 m1A Human chr14 - 91399148 91399148 91399148 CTCAAGAGTCACAAGCAGGCATGGAGAATGAGAACTGCCCATGGCCAAGGAGGTGGGAGCAGGCC CTCAAGAGTCACAAGCAGGCATGGAGAATGAGGACTGCCCATGGCCAAGGAGGTGGGAGCAGGCC T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:91399137..91399364 26863196 MeRIP-seq:(Medium) rs920626310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49370,RMVar_hsa_circ_66874,RMVar_hsa_circ_121341,RMVar_hsa_circ_168589 60836 RMVar_ID_60836 Human_SNP_ID_565015001 m1A Human chr14 - 91510065 91510065 91510065 ACTGGCCGCGGTGGCAGGGCCAGGTATAAGGAAGGAAAATATGGCGGCGGCGGCGGCGGCCTGAG ACTGGCCGCGGTGGCAGGGCCAGGTATAAGGACGGAAAATATGGCGGCGGCGGCGGCGGCCTGAG T G PPP4R3A Ensembl:ENSG00000100796 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:91510056..91510254 26863196 MeRIP-seq:(Medium) rs1293083979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4483,Human_RBP_ID_40703,Human_RBP_ID_4305212,Human_RBP_ID_5522864,Human_RBP_ID_8941062,Human_RBP_ID_9323834 60837 RMVar_ID_60837 Human_SNP_ID_565137733 m1A Human chr14 + 92026751 92026748 92026751 CAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGAAGAAGAAGGTGAGGGTGAGGAAGAAGGATGGAG CAGGAAGAAGGTGGGGAGGAAGAGGAGGAG___GAAGAAGGTGAGGGTGAGGAAGAAGGATGGAG GGAA G AL049872.1 Ensembl:ENSG00000259020 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:92026621..92026876 26863196 MeRIP-seq:(Medium) rs776707608 Functional Loss DEL dbSNP153 31..33 33 - - - 60838 RMVar_ID_60838 Human_SNP_ID_565137734 m1A Human chr14 + 92026751 92026751 92026751 CAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGAAGAAGAAGGTGAGGGTGAGGAAGAAGGATGGAG CAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGAGGAAGAAGGTGAGGGTGAGGAAGAAGGATGGAG A G AL049872.1 Ensembl:ENSG00000259020 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:92026621..92026876 26863196 MeRIP-seq:(Medium) rs1223963133 Functional Loss SNV dbSNP153 33..33 33 - - - 60839 RMVar_ID_60839 Human_SNP_ID_565141679 m1A Human chr14 - 92042262 92042262 92042262 TCAGCTTAATCTCTCCCACTCTAGGTTCCCACACCACCCCTAATACCGCTCGAAGCAGCCCTGAG TCAGCTTAATCTCTCCCACTCTAGGTTCCCACGCCACCCCTAATACCGCTCGAAGCAGCCCTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92042231..92042296 26863196 MeRIP-seq:(Medium) rs11849081 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7359 60840 RMVar_ID_60840 Human_SNP_ID_565142275 m1A Human chr14 - 92044145 92044145 92044145 TGCACCTACACAGCTGCCCCCGCCTTATATACAGACTGGGCAACATCTCCTGTCTCCCTACACCT TGCACCTACACAGCTGCCCCCGCCTTATATACGGACTGGGCAACATCTCCTGTCTCCCTACACCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:92044102..92044238 26863196 MeRIP-seq:(Medium) rs1356180493 Functional Loss SNV dbSNP153 33..33 33 - - - 60841 RMVar_ID_60841 Human_SNP_ID_565142782 m1A Human chr14 + 92046350 92046350 92046350 ATAAACCAAGTGTGATCAGGGTGAGGAATAGGAAAGAAGGAAGTATGGGGAAATGGAGTGAATGC ATAAACCAAGTGTGATCAGGGTGAGGAATAGGGAAGAAGGAAGTATGGGGAAATGGAGTGAATGC A G lnc-CPSF2-5 RNACentral:URS0000D57E9E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92046299..92046406 26863196 MeRIP-seq:(Medium) rs201720188 Functional Loss SNV dbSNP153 33..33 33 - - - 60842 RMVar_ID_60842 Human_SNP_ID_565143256 m1A Human chr14 - 92048737 92048737 92048737 ATTCTTCCTCAGCCTCCGGTCCCCCACCCTATAATCCTTTTATCACCCCCTCCTCACACCGTGTC ATTCTTCCTCAGCCTCCGGTCCCCCACCCTATCATCCTTTTATCACCCCCTCCTCACACCGTGTC T G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:92048694..92048938 26863196 MeRIP-seq:(Medium) rs1227997449 Functional Loss SNV dbSNP153 33..33 33 - - - 60843 RMVar_ID_60843 Human_SNP_ID_565145741 m1A Human chr14 - 92059399 92059399 92059399 AGCAATGTAAATAACTTTATTTTTCATATTCAAAATAAAAACTTTCTTTTATTTCTGGCCCCTTT AGCAATGTAAATAACTTTATTTTTCATATTCAGAATAAAAACTTTCTTTTATTTCTGGCCCCTTT T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs116994678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6395723,Human_RBP_ID_26629510,Human_RBP_ID_27648612 60844 RMVar_ID_60844 Human_SNP_ID_565161214 m1A Human chr14 + 92117641 92117641 92117641 TCCCGCACAATCTGAAGTAAGTTCACCATGATAGCTAAAAGAAAAAAAAATTATCAGAAATACAA TCCCGCACAATCTGAAGTAAGTTCACCATGATGGCTAAAAGAAAAAAAAATTATCAGAAATACAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92117626..92117650 26863196 MeRIP-seq:(Medium) rs1342769682 Functional Loss SNV dbSNP153 33..33 33 - - - 60845 RMVar_ID_60845 Human_SNP_ID_565162281 m1A Human chr14 - 92121280 92121280 92121280 CCTCCCCTCCGCGAGCAGCTTACATTCGTCCAAGTTCCAGCCTTCTGTCTTCTCGCTAACCTCGC CCTCCCCTCCGCGAGCAGCTTACATTCGTCCAGGTTCCAGCCTTCTGTCTTCTCGCTAACCTCGC T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:92121277..92121376 26863196 MeRIP-seq:(Medium) rs571054513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3465901 Human_Splice_Rec_1547239,Human_Splice_Rec_1547247 GWAS_ID_7360 60846 RMVar_ID_60846 Human_SNP_ID_565162338 m1A Human chr14 + 92121460 92121460 92121460 TCAGAAAACCCTTTCCAAAAGCTCCGGCCCGGAAATCCCATCCTCCACCCGAAGAAAACCCCATT TCAGAAAACCCTTTCCAAAAGCTCCGGCCCGGCAATCCCATCCTCCACCCGAAGAAAACCCCATT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92121451..92121944 26863196 MeRIP-seq:(Medium) rs7143338 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7361,GWAS_ID_7362,GWAS_ID_7363,GWAS_ID_7364,GWAS_ID_7365,GWAS_ID_7366,GWAS_ID_7367 60847 RMVar_ID_60847 Human_SNP_ID_565164297 m1A Human chr14 + 92128730 92128730 92128730 AAAGTAGTCAGCGAATTAGAGAGATACCACTGACCCCAGAGGATTTTTGCAATGGGAATACTAGA AAAGTAGTCAGCGAATTAGAGAGATACCACTGGCCCCAGAGGATTTTTGCAATGGGAATACTAGA A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:92128722..92129070 26863196 MeRIP-seq:(Medium) rs530129559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12444637,Human_RBP_ID_18658828 RMVar_hsa_circ_23131,RMVar_hsa_circ_109463,RMVar_hsa_circ_168661,RMVar_hsa_circ_90785,RMVar_hsa_circ_168660,RMVar_hsa_circ_50899,RMVar_hsa_circ_281926,RMVar_hsa_circ_304851,RMVar_hsa_circ_305029,RMVar_hsa_circ_269781,RMVar_hsa_circ_39866,RMVar_hsa_circ_168663 60848 RMVar_ID_60848 Human_SNP_ID_565164329 m1A Human chr14 + 92128895 92128895 92128895 GGCTGAAGTGAAATGATTATTGGAGTTGAGGAAGTCAAGGAACCAACAGGTCAGTATTGAAGTTA GGCTGAAGTGAAATGATTATTGGAGTTGAGGAGGTCAAGGAACCAACAGGTCAGTATTGAAGTTA A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:92128637..92129107 26863196 MeRIP-seq:(Medium) rs1200418088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12444646 RMVar_hsa_circ_23131,RMVar_hsa_circ_109463,RMVar_hsa_circ_168661,RMVar_hsa_circ_90785,RMVar_hsa_circ_168660,RMVar_hsa_circ_50899,RMVar_hsa_circ_281926,RMVar_hsa_circ_304851,RMVar_hsa_circ_305029,RMVar_hsa_circ_269781,RMVar_hsa_circ_39866,RMVar_hsa_circ_168663 60849 RMVar_ID_60849 Human_SNP_ID_565258234 m1A Human chr14 + 92513740 92513739 92513740 TTTTGACAAAAAAACCCTTGACCACCAAGGCCAGCCTCTTCCTGAAAGCCCCGCTCGCTCCGATA TTTTGACAAAAAAACCCTTGACCACCAAGGCC_GCCTCTTCCTGAAAGCCCCGCTCGCTCCGATA CA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:92513654..92513883 26863410 MeRIP-seq:(Medium) rs950391453 Functional Loss DEL dbSNP153 33..33 33 - - - 60850 RMVar_ID_60850 Human_SNP_ID_565292463 m1A Human chr14 + 92652322 92652322 92652322 CTCCCCAAGGGACCTCAGACGGCCCTGAGGACACGCCCCGGGAGAGCACGGAGCAAGGCCAGGAC CTCCCCAAGGGACCTCAGACGGCCCTGAGGACGCGCCCCGGGAGAGCACGGAGCAAGGCCAGGAC A G RIN3 Ensembl:ENSG00000100599 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:92652271..92652385 32194978 MeRIP-seq:(Medium) rs1222512832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_542,RMVar_hsa_circ_73897,RMVar_hsa_circ_46320,RMVar_hsa_circ_355106,RMVar_hsa_circ_28619,RMVar_hsa_circ_168683,RMVar_hsa_circ_377829 60851 RMVar_ID_60851 Human_SNP_ID_565294370 m1A Human chr14 + 92659464 92659464 92659464 CAAACTCATCTACGACTCCATGGCCCTCGGCAACCCAGGTCAGTGGGCAGCCGGGAGGGGTCTGG CAAACTCATCTACGACTCCATGGCCCTCGGCAGCCCAGGTCAGTGGGCAGCCGGGAGGGGTCTGG A G RIN3 Ensembl:ENSG00000100599 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:92659367..92676572 32194978 MeRIP-seq:(Medium) rs1046031104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19064282 Human_Splice_Rec_1547491,Human_Splice_Rec_1547507,Human_Splice_Rec_1547527,Human_Splice_Rec_1547549,Human_Splice_Rec_1547569,Human_Splice_Rec_1547573 RMVar_hsa_circ_542,RMVar_hsa_circ_73897,RMVar_hsa_circ_46320,RMVar_hsa_circ_28619,RMVar_hsa_circ_332367 60852 RMVar_ID_60852 Human_SNP_ID_565307608 m1A Human chr14 - 92709847 92709847 92709847 TCCCCAGACAATCTCCACCATGAAAGTGATGCAGTTTCAGGGTATGAAACGCAAAGCCAGTTCTC TCCCCAGACAATCTCCACCATGAAAGTGATGCCGTTTCAGGGTATGAAACGCAAAGCCAGTTCTC T G LGMN Ensembl:ENSG00000100600 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:92709798..92715773 32194978 MeRIP-seq:(Medium) rs775353273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_453786,Human_RBP_ID_19994399 Human_Splice_Rec_1547598,Human_Splice_Rec_1547620,Human_Splice_Rec_1547648,Human_Splice_Rec_1547674,Human_Splice_Rec_1547698,Human_Splice_Rec_1547712 Human_miRNA_ID_619110,Human_miRNA_ID_2235154,Human_miRNA_ID_2452550,Human_miRNA_ID_3029317 RMVar_hsa_circ_29997,RMVar_hsa_circ_107561,RMVar_hsa_circ_299628,RMVar_hsa_circ_316872,RMVar_hsa_circ_168684,RMVar_hsa_circ_307632,RMVar_hsa_circ_47755,RMVar_hsa_circ_168685,RMVar_hsa_circ_168686 60853 RMVar_ID_60853 Human_SNP_ID_565310225 m1A Human chr14 + 92719302 92719272 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCG______________________________CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCGCCACCGCCGCCGCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1566924356 Functional Loss DEL dbSNP153 4..33 33 - - - 60854 RMVar_ID_60854 Human_SNP_ID_565310232 m1A Human chr14 + 92719302 92719275 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCG___________________________CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCACCGCCGCCGCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1267969098 Functional Loss DEL dbSNP153 7..33 33 - - - 60855 RMVar_ID_60855 Human_SNP_ID_565310252 m1A Human chr14 + 92719302 92719284 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCG__________________CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCGCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1566924435 Functional Loss DEL dbSNP153 16..33 33 - - - 60856 RMVar_ID_60856 Human_SNP_ID_565310258 m1A Human chr14 + 92719302 92719287 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCG_______________CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1566924459 Functional Loss DEL dbSNP153 19..33 33 - - - 60857 RMVar_ID_60857 Human_SNP_ID_565310267 m1A Human chr14 + 92719302 92719290 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCGCCG____________CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1566924472 Functional Loss DEL dbSNP153 22..33 33 - - - 60858 RMVar_ID_60858 Human_SNP_ID_565310286 m1A Human chr14 + 92719302 92719296 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCGCCGCCGCCG______CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1566924522 Functional Loss DEL dbSNP153 28..33 33 - - - 60859 RMVar_ID_60859 Human_SNP_ID_565310292 m1A Human chr14 + 92719302 92719299 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCGCCGCCGCCGCCG___CCGCCGCCACCGCCGCCGCCGCCACCGCCACC GCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs1180586672 Functional Loss DEL dbSNP153 31..33 33 - - - 60860 RMVar_ID_60860 Human_SNP_ID_565310296 m1A Human chr14 + 92719302 92719302 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCCCGCCGCCACCGCCGCCGCCGCCACCGCCACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs184843394 Functional Loss SNV dbSNP153 33..33 33 - - - 60861 RMVar_ID_60861 Human_SNP_ID_565310297 m1A Human chr14 + 92719302 92719302 92719302 CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCGCCGCCGCCACCGCCACC CCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCGCCACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:92719226..92719361;chr14:92719178..92719416;chr14:92719251..92719418;chr14:92719178..92719397;chr14:92719223..92719332;chr14:92719211..92719312;chr14:92719251..92719325;chr14:92719175..92719400 26863196 MeRIP-seq:(Medium) rs184843394 Functional Loss SNV dbSNP153 33..33 33 - - - 60862 RMVar_ID_60862 Human_SNP_ID_565312721 m1A Human chr14 - 92729211 92729211 92729211 ACAGAGGCAGACCTGGGAGAGGGGCCAGCAAGATGGGCCAGGATGGGCAGAGGTGCGCAGGCACC ACAGAGGCAGACCTGGGAGAGGGGCCAGCAAGGTGGGCCAGGATGGGCAGAGGTGCGCAGGCACC T C LGMN Ensembl:ENSG00000100600 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:92729206..92729318 26863196 MeRIP-seq:(Medium) rs531528881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813089 RMVar_hsa_circ_96704,RMVar_hsa_circ_107561,RMVar_hsa_circ_168684,RMVar_hsa_circ_168691,RMVar_hsa_circ_168690,RMVar_hsa_circ_101640,RMVar_hsa_circ_330570 60863 RMVar_ID_60863 Human_SNP_ID_565313678 m1A Human chr14 + 92732755 92732755 92732755 CATCTATAGGAACGGCACCAATGCCCAGGGCCACACTGAGGAATACAGCTACTTTCCAAACCATT CATCTATAGGAACGGCACCAATGCCCAGGGCCGCACTGAGGAATACAGCTACTTTCCAAACCATT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92732706..92732857 26863196 MeRIP-seq:(Medium) rs1566933160 Functional Loss SNV dbSNP153 33..33 33 - - - 60864 RMVar_ID_60864 Human_SNP_ID_565313695 m1A Human chr14 - 92732802 92732802 92732802 TCTGTGTTTCCCTTCTCAGGTGTCTGCAATTGAACTCCAAGGTGCAGAATGGTTTGGAAAGTAGC TCTGTGTTTCCCTTCTCAGGTGTCTGCAATTGCACTCCAAGGTGCAGAATGGTTTGGAAAGTAGC T G LGMN Ensembl:ENSG00000100600 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:92732708..92732866 26863196 MeRIP-seq:(Medium) rs145591815 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3466011 Human_Splice_Rec_1547580,Human_Splice_Rec_1547602,Human_Splice_Rec_1547630,Human_Splice_Rec_1547656,Human_Splice_Rec_1547682,Human_Splice_Rec_1547716,Human_Splice_Rec_1547734,Human_Splice_Rec_1547744,Human_Splice_Rec_1547754,Human_Splice_Rec_1547764,Human_Splice_Rec_1547770,Human_Splice_Rec_1547778,Human_Splice_Rec_1547784,Human_Splice_Rec_1547788,Human_Splice_Rec_1547792 Human_miRNA_ID_2615746,Human_miRNA_ID_2750894 RMVar_hsa_circ_96704,RMVar_hsa_circ_107561,RMVar_hsa_circ_168684,RMVar_hsa_circ_168691,RMVar_hsa_circ_168690,RMVar_hsa_circ_101640,RMVar_hsa_circ_330570 60865 RMVar_ID_60865 Human_SNP_ID_565339021 m1A Human chr14 + 92834880 92834880 92834880 CGGAGGTGGGTGGGTAGCCATTGCATTAATCCATGTGAGAGATGGTAGTCTAGAACTGAGTGGGA CGGAGGTGGGTGGGTAGCCATTGCATTAATCCGTGTGAGAGATGGTAGTCTAGAACTGAGTGGGA A G GOLGA5 Ensembl:ENSG00000066455 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:92834837..92834920 26863196 MeRIP-seq:(Medium) rs574148683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10526,RMVar_hsa_circ_44663,RMVar_hsa_circ_299001,RMVar_hsa_circ_168700,RMVar_hsa_circ_168701,RMVar_hsa_circ_346213,RMVar_hsa_circ_67711,RMVar_hsa_circ_338297,RMVar_hsa_circ_168704 60866 RMVar_ID_60866 Human_SNP_ID_565365336 m1A Human chr14 - 92940081 92940081 92940081 CTGCAGGATGCCCACTTTGAGGAGGGAGGCACAGGGCTTGGGCGAGGGGCAGAGGCCATCAGAAC CTGCAGGATGCCCACTTTGAGGAGGGAGGCACGGGGCTTGGGCGAGGGGCAGAGGCCATCAGAAC T C ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92940031..92940131 26863196 MeRIP-seq:(Medium) rs1252616680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2429851,Human_RBP_ID_6396521,Human_RBP_ID_8797203,Human_RBP_ID_26432187 Human_miRNA_ID_177095,Human_miRNA_ID_864376,Human_miRNA_ID_975592 RMVar_hsa_circ_168705,RMVar_hsa_circ_90755 60867 RMVar_ID_60867 Human_SNP_ID_565365422 m1A Human chr14 + 92940501 92940499 92940501 ACCTGCTGGCTCAGTGCTTGGGGCTTGCAATGAGAGGTGGACCAGGCCTGCTGGGTGAGGAGGGA ACCTGCTGGCTCAGTGCTTGGGGCTTGCAAT__GAGGTGGACCAGGCCTGCTGGGTGAGGAGGGA TGA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:92940354..92941402 32194978 MeRIP-seq:(Medium) rs934373931 Functional Loss DEL dbSNP153 32..33 33 - - - 60868 RMVar_ID_60868 Human_SNP_ID_565398780 m1A Human chr14 - 93076098 93076098 93076098 AGGTGGACAGATGGAGGGAGAAGGAAGGATGGAGGGAGAAGGAAGGATGGATGGAGGGGAGGAAG AGGTGGACAGATGGAGGGAGAAGGAAGGATGGCGGGAGAAGGAAGGATGGATGGAGGGGAGGAAG T G ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:93076095..93076197 26863196 MeRIP-seq:(Medium) rs1442863897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82381,RMVar_hsa_circ_168714,RMVar_hsa_circ_328829,RMVar_hsa_circ_168715 60869 RMVar_ID_60869 Human_SNP_ID_565408760 m1A Human chr14 + 93115198 93115198 93115198 TCCTCCTCGGGCGGGGAGCCTGGGTCCGGAGGAAATCGCCCACAGGCCGAGTCTGGCGGCCGGCG TCCTCCTCGGGCGGGGAGCCTGGGTCCGGAGGCAATCGCCCACAGGCCGAGTCTGGCGGCCGGCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:93115157..93115284 26863196 MeRIP-seq:(Medium) rs1254174401 Functional Loss SNV dbSNP153 33..33 33 - - - 60870 RMVar_ID_60870 Human_SNP_ID_565408790 m1A Human chr14 + 93115251 93115251 93115251 TGGCGGCCGGCGCGCGCCGCGAGCGAGTGGGCACCTCCTCCCGGCGGCGGGGACGCGGAACGGGG TGGCGGCCGGCGCGCGCCGCGAGCGAGTGGGCCCCTCCTCCCGGCGGCGGGGACGCGGAACGGGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:93115174..93115370 26863410 MeRIP-seq:(Medium) rs1248596656 Functional Loss SNV dbSNP153 33..33 33 - - - 60871 RMVar_ID_60871 Human_SNP_ID_565408819 m1A Human chr14 - 93115307 93115307 93115307 GCCGCGCCCCGCCCCGCTCCGCTCCGCGCGGCAGGACTGCGCGCCCCAGCTCCGATCCCCGTTCC GCCGCGCCCCGCCCCGCTCCGCTCCGCGCGGCGGGACTGCGCGCCCCAGCTCCGATCCCCGTTCC T C ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:93115236..93115366 26863410 MeRIP-seq:(Medium) rs1390182086 Functional Loss SNV dbSNP153 33..33 33 - - - 60872 RMVar_ID_60872 Human_SNP_ID_565408820 m1A Human chr14 - 93115307 93115307 93115307 GCCGCGCCCCGCCCCGCTCCGCTCCGCGCGGCAGGACTGCGCGCCCCAGCTCCGATCCCCGTTCC GCCGCGCCCCGCCCCGCTCCGCTCCGCGCGGCCGGACTGCGCGCCCCAGCTCCGATCCCCGTTCC T G ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:93115236..93115366 26863410 MeRIP-seq:(Medium) rs1390182086 Functional Loss SNV dbSNP153 33..33 33 - - - 60873 RMVar_ID_60873 Human_SNP_ID_565409028 m1A Human chr14 + 93115853 93115853 93115853 CCGCCGAGAAGGGCGGCGGCGAGCGCCCGCGCACTCGCCGCCCCTGCCCGCCGCCGCCCCGCGCT CCGCCGAGAAGGGCGGCGGCGAGCGCCCGCGCGCTCGCCGCCCCTGCCCGCCGCCGCCCCGCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:93115627..93115925;chr14:93115639..93115876 26863196 MeRIP-seq:(Medium) rs1208886390 Functional Loss SNV dbSNP153 33..33 33 - - - 60874 RMVar_ID_60874 Human_SNP_ID_565409029 m1A Human chr14 + 93115853 93115853 93115853 CCGCCGAGAAGGGCGGCGGCGAGCGCCCGCGCACTCGCCGCCCCTGCCCGCCGCCGCCCCGCGCT CCGCCGAGAAGGGCGGCGGCGAGCGCCCGCGCTCTCGCCGCCCCTGCCCGCCGCCGCCCCGCGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:93115627..93115925;chr14:93115639..93115876 26863196 MeRIP-seq:(Medium) rs1208886390 Functional Loss SNV dbSNP153 33..33 33 - - - 60875 RMVar_ID_60875 Human_SNP_ID_565429148 m1A Human chr14 - 93184713 93184713 93184713 GACTGTCATCGCCCCATCACTTCTCGTTGCAGACAGTACCACAGGCACCTGGAGTACCGGCATCG GACTGTCATCGCCCCATCACTTCTCGTTGCAGGCAGTACCACAGGCACCTGGAGTACCGGCATCG T C MOAP1 Ensembl:ENSG00000165943 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:93184671..93184840 26863196 MeRIP-seq:(Medium) rs1363421096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882175,Human_RBP_ID_1501170,Human_RBP_ID_5352389 Human_Splice_Rec_1548052 60876 RMVar_ID_60876 Human_SNP_ID_565429177 m1A Human chr14 + 93184814 93184814 93184814 GAGTCGCCAGACCCAGAGAGCCACCCACCTGGAGGGACGTGCCGCCACCCGCGCCGCCGGAGCTC GAGTCGCCAGACCCAGAGAGCCACCCACCTGGGGGGACGTGCCGCCACCCGCGCCGCCGGAGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:93184572..93184843 26863196 MeRIP-seq:(Medium) rs1010944379 Functional Loss SNV dbSNP153 33..33 33 - - - 60877 RMVar_ID_60877 Human_SNP_ID_565434766 m1A Human chr14 - 93206868 93206868 93206868 ATTATTCGACCCTCTGGTACAGGGGGAAGTGCAGCACCGGGTGGCGGCGGCTCCAGACGAGGACT ATTATTCGACCCTCTGGTACAGGGGGAAGTGCGGCACCGGGTGGCGGCGGCTCCAGACGAGGACT T C GON7 Ensembl:ENSG00000170270 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:93203758..93207050 26863196 MeRIP-seq:(Medium) rs747691161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1548087 60878 RMVar_ID_60878 Human_SNP_ID_565434792 m1A Human chr14 + 93206951 93206951 93206951 ATCTGGGCCACGCCAGACAACAGGCCCTGGAAAGGGTCGCCGTCACCCGGCGCCTCACAGGACAC ATCTGGGCCACGCCAGACAACAGGCCCTGGAAGGGGTCGCCGTCACCCGGCGCCTCACAGGACAC A G AL110118.2 Ensembl:ENSG00000259066 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:93203662..93206950 32194978 MeRIP-seq:(Medium) rs200749263 Functional Loss SNV dbSNP153 33..33 33 - - - 60879 RMVar_ID_60879 Human_SNP_ID_565435031 m1A Human chr14 + 93207305 93207305 93207305 GTTCGGCTGACAGTTGAGGATGGCCGGAGCCGAGGGCGCCGCTGGGCGGCAGTCGGAGCTGGAGC GTTCGGCTGACAGTTGAGGATGGCCGGAGCCGTGGGCGCCGCTGGGCGGCAGTCGGAGCTGGAGC A T AL110118.2,UBR7 Ensembl:ENSG00000259066,Ensembl:ENSG00000012963 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:93207251..93207384;chr14:93207251..93207405;chr14:93207251..93209846 26863196 MeRIP-seq:(Medium) rs1457382060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1501189,Human_RBP_ID_4308479,Human_RBP_ID_23641804 60880 RMVar_ID_60880 Human_SNP_ID_565443565 m1A Human chr14 - 93240209 93240209 93240209 TGGTTAGCTGCTGTGCGGGTGCGCTCGGTGACACTGGTGGTGGTGCACGCTCCCGAGCTCCCAGA TGGTTAGCTGCTGTGCGGGTGCGCTCGGTGACGCTGGTGGTGGTGCACGCTCCCGAGCTCCCAGA T C BTBD7 Ensembl:ENSG00000011114 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8013451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6396879 Human_miRNA_ID_504436,Human_miRNA_ID_511649,Human_miRNA_ID_2175446,Human_miRNA_ID_2178889 GWAS_ID_7368,GWAS_ID_7369 RMVar_hsa_circ_106641,RMVar_hsa_circ_110334,RMVar_hsa_circ_168727,RMVar_hsa_circ_168729,RMVar_hsa_circ_94171,RMVar_hsa_circ_168728 60881 RMVar_ID_60881 Human_SNP_ID_565445130 m1A Human chr14 - 93246038 93246038 93246038 TGGAAGCAAAGACCTCCCAGTCAGCACCCTTCACGTTCATTTTCTTATCCCTGTAATCATTCGCT TGGAAGCAAAGACCTCCCAGTCAGCACCCTTCCCGTTCATTTTCTTATCCCTGTAATCATTCGCT T G BTBD7 Ensembl:ENSG00000011114 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:93245989..93246079 26863196 MeRIP-seq:(Medium) rs375634897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18937531 RMVar_hsa_circ_106641,RMVar_hsa_circ_110334,RMVar_hsa_circ_23150,RMVar_hsa_circ_168727,RMVar_hsa_circ_168729,RMVar_hsa_circ_94171,RMVar_hsa_circ_168728,RMVar_hsa_circ_122664,RMVar_hsa_circ_264930,RMVar_hsa_circ_168730 60882 RMVar_ID_60882 Human_SNP_ID_565466678 m1A Human chr14 + 93332914 93332902 93332914 CCGCCACCAGCACCGCCGTCCGCACCGGCGCCAGCACCCCCGGCCATCCTCCTCCCACCGCCGCC CCGCCACCAGCACCGCCGTCC____________GCACCCCCGGCCATCCTCCTCCCACCGCCGCC CGCACCGGCGCCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:93332665..93333048 26863196 MeRIP-seq:(Medium) rs1242030102 Functional Loss DEL dbSNP153 22..33 33 - - - 60883 RMVar_ID_60883 Human_SNP_ID_565466757 m1A Human chr14 - 93333000 93333000 93333000 TCCGTCTAGGAGTCAAAATGGCGGCGAGGGGAACCTGGAGCAGTCCCGGAGCCTGAGCCACTGAC TCCGTCTAGGAGTCAAAATGGCGGCGAGGGGAGCCTGGAGCAGTCCCGGAGCCTGAGCCACTGAC T C BTBD7 Ensembl:ENSG00000011114 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:93332640..93333036;chr14:93296074..93333063 26863196 MeRIP-seq:(Medium) rs1233659179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106641,RMVar_hsa_circ_168727 60884 RMVar_ID_60884 Human_SNP_ID_565639844 m1A Human chr14 - 94051390 94051390 94051390 GCAGATGAAGGTTCTGAAGAAGGAGCTGCGCCACCTGCTGTCCCAGCCACTGTTTACGGAGAGCC GCAGATGAAGGTTCTGAAGAAGGAGCTGCGCCCCCTGCTGTCCCAGCCACTGTTTACGGAGAGCC T G DDX24 Ensembl:ENSG00000089737 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:94051301..94051770 32194978 MeRIP-seq:(Medium) rs749037973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38973,Human_RBP_ID_880637,Human_RBP_ID_1501365,Human_RBP_ID_1826317,Human_RBP_ID_3466331,Human_RBP_ID_3944634,Human_RBP_ID_4315211,Human_RBP_ID_6397460,Human_RBP_ID_8412725,Human_RBP_ID_9369335,Human_RBP_ID_18659118 Human_Splice_Rec_1549002,Human_Splice_Rec_1549016,Human_Splice_Rec_1549018,Human_Splice_Rec_1549034,Human_Splice_Rec_1549050,Human_Splice_Rec_1549062,Human_Splice_Rec_1549078,Human_Splice_Rec_1549094,Human_Splice_Rec_1549096 Human_miRNA_ID_2222518,Human_miRNA_ID_2485574,Human_miRNA_ID_3073950 RMVar_hsa_circ_94544,RMVar_hsa_circ_120930,RMVar_hsa_circ_168812,RMVar_hsa_circ_168813 60885 RMVar_ID_60885 Human_SNP_ID_565639876 m1A Human chr14 - 94051455 94051455 94051455 GATCGTTTTTGTATTGTGTTTCAAGGAGGAAAAGCTGACCAGCAAGAAGAACGTCGGAGACAAAA GATCGTTTTTGTATTGTGTTTCAAGGAGGAAAGGCTGACCAGCAAGAAGAACGTCGGAGACAAAA T C DDX24 Ensembl:ENSG00000089737 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94051083..94051483 26863196 MeRIP-seq:(Medium) rs754810856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880637,Human_RBP_ID_1501366,Human_RBP_ID_2430200,Human_RBP_ID_3944635,Human_RBP_ID_9369335,Human_RBP_ID_17651221 Human_Splice_Rec_1549002,Human_Splice_Rec_1549016,Human_Splice_Rec_1549018,Human_Splice_Rec_1549034,Human_Splice_Rec_1549050,Human_Splice_Rec_1549062,Human_Splice_Rec_1549078,Human_Splice_Rec_1549094,Human_Splice_Rec_1549096 RMVar_hsa_circ_94544,RMVar_hsa_circ_120930,RMVar_hsa_circ_168812,RMVar_hsa_circ_168813 60886 RMVar_ID_60886 Human_SNP_ID_565640874 m1A Human chr14 - 94055354 94055354 94055354 GCCTACACAGTGAATGGGCTAAACCTGGGAACATTTTGAATGTGGGACTAAGAGAGGAGGGCTAG GCCTACACAGTGAATGGGCTAAACCTGGGAACGTTTTGAATGTGGGACTAAGAGAGGAGGGCTAG T C DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:94055235..94055573 26863196 MeRIP-seq:(Medium) rs79099449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2430209,Human_RBP_ID_6397482,Human_RBP_ID_12447728,Human_RBP_ID_23642076 RMVar_hsa_circ_120930,RMVar_hsa_circ_168813 60887 RMVar_ID_60887 Human_SNP_ID_565640977 m1A Human chr14 - 94055833 94055833 94055833 GTGTTCAGGGGCACTTGGCTCACAGTGAGAAGAGGGTATGTGTTGGGAAAGGAATAGTTGCTGAG GTGTTCAGGGGCACTTGGCTCACAGTGAGAAGGGGGTATGTGTTGGGAAAGGAATAGTTGCTGAG T C DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94055793..94055885 26863196 MeRIP-seq:(Medium) rs971746438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6397497 RMVar_hsa_circ_120930,RMVar_hsa_circ_168813 60888 RMVar_ID_60888 Human_SNP_ID_565640978 m1A Human chr14 - 94055833 94055833 94055833 GTGTTCAGGGGCACTTGGCTCACAGTGAGAAGAGGGTATGTGTTGGGAAAGGAATAGTTGCTGAG GTGTTCAGGGGCACTTGGCTCACAGTGAGAAGCGGGTATGTGTTGGGAAAGGAATAGTTGCTGAG T G DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94055793..94055885 26863196 MeRIP-seq:(Medium) rs971746438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6397497 RMVar_hsa_circ_120930,RMVar_hsa_circ_168813 60889 RMVar_ID_60889 Human_SNP_ID_565647600 m1A Human chr14 + 94081170 94081170 94081170 AGCTCCGTCAGTCGCGAGTGAAGAACCTCAGAAACCGCCGCTGTACCTCAGCTGCAGCAGCAACT AGCTCCGTCAGTCGCGAGTGAAGAACCTCAGACACCGCCGCTGTACCTCAGCTGCAGCAGCAACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:94081072..94081200;chr14:94081101..94081200 26863196 MeRIP-seq:(Medium) rs1484454500 Functional Loss SNV dbSNP153 33..33 33 - - - 60890 RMVar_ID_60890 Human_SNP_ID_565647715 m1A Human chr14 + 94081423 94081423 94081423 AAGGTGAAATTCTGTGTGCTCCCTCCGGCGAGAGACTTTGTCAGCTCCCGCACAGTAACGTAAGT AAGGTGAAATTCTGTGTGCTCCCTCCGGCGAGGGACTTTGTCAGCTCCCGCACAGTAACGTAAGT A G IFI27L1 Ensembl:ENSG00000165948 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94081372..94081483 26863196 MeRIP-seq:(Medium) rs1299608206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_454006,Human_RBP_ID_4308484,Human_RBP_ID_23642126 Human_Splice_Rec_1549099,Human_Splice_Rec_1549103,Human_Splice_Rec_1549111,Human_Splice_Rec_1549115,Human_Splice_Rec_1549123,Human_Splice_Rec_1549127,Human_Splice_Rec_1549137,Human_Splice_Rec_1549147,Human_Splice_Rec_1549157,Human_Splice_Rec_1549167,Human_Splice_Rec_1549173,Human_Splice_Rec_1549177 60891 RMVar_ID_60891 Human_SNP_ID_565651530 m1A Human chr14 + 94097555 94097555 94097555 GATGGATTCCGGGTTCAGCAGTGACTTGGGCCAGAGCAGAGGCAGAGAGACAAGTTAGGAAGCTC GATGGATTCCGGGTTCAGCAGTGACTTGGGCCGGAGCAGAGGCAGAGAGACAAGTTAGGAAGCTC A G IFI27L1 Ensembl:ENSG00000165948 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:94097549..94097715 26863196 MeRIP-seq:(Medium) rs990645273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6397682,Human_RBP_ID_12448161 Human_Splice_Rec_1549130,Human_Splice_Rec_1549140,Human_Splice_Rec_1549160 60892 RMVar_ID_60892 Human_SNP_ID_565651739 m1A Human chr14 + 94098286 94098286 94098286 GCCCTTCAGGAGAATGTTCCATGCCACTCCCTAGTTTCTGGTGGCTGCTGTCAGTCTTCGACGTC GCCCTTCAGGAGAATGTTCCATGCCACTCCCTGGTTTCTGGTGGCTGCTGTCAGTCTTCGACGTC A G IFI27L1 Ensembl:ENSG00000165948 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1487713000 Functional Loss SNV dbSNP153 33..33 33 - - - 60893 RMVar_ID_60893 Human_SNP_ID_565651932 m1A Human chr14 - 94099153 94099153 94099153 GCTGGGCCCACCTGCTATTCCTACTCCAAGTCATGCTCCAGCAGTGCCTCCCTCGCTTCTGCATC GCTGGGCCCACCTGCTATTCCTACTCCAAGTCGTGCTCCAGCAGTGCCTCCCTCGCTTCTGCATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94099150..94099304 26863196 MeRIP-seq:(Medium) rs374085255 Functional Loss SNV dbSNP153 33..33 33 - - - 60894 RMVar_ID_60894 Human_SNP_ID_565659240 m1A Human chr14 + 94128503 94128503 94128503 TGGATCTTCTCGCAGCTCTGGTGGTCCTGTCTAGGACACTTACCCACGGACTGCAGAGTAGCCAC TGGATCTTCTCGCAGCTCTGGTGGTCCTGTCTGGGACACTTACCCACGGACTGCAGAGTAGCCAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:94128501..94128675 32194978 MeRIP-seq:(Medium) rs769173307 Functional Loss SNV dbSNP153 33..33 33 - - - 60895 RMVar_ID_60895 Human_SNP_ID_565659314 m1A Human chr14 + 94128651 94128651 94128651 CTGCCCCAGTGAAGCCCATGGCACTGAGCACCACGGGCACAGCCCCCACTGCCAGGGCTGTGGGG CTGCCCCAGTGAAGCCCATGGCACTGAGCACCCCGGGCACAGCCCCCACTGCCAGGGCTGTGGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:94128600..94128672 26863196 MeRIP-seq:(Medium) rs781454612 Functional Loss SNV dbSNP153 33..33 33 - - - 60896 RMVar_ID_60896 Human_SNP_ID_565659591 m1A Human chr14 - 94129492 94129492 94129492 GGGCTGGGGGCAGGCTTCCCCAACCCCAGCCCAGGAAGGGACAGGGAATAGCTTCATTCCCTGAC GGGCTGGGGGCAGGCTTCCCCAACCCCAGCCCGGGAAGGGACAGGGAATAGCTTCATTCCCTGAC T C IFI27L2 Ensembl:ENSG00000119632 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:94129490..94129576 26863196 MeRIP-seq:(Medium) rs540245814 Functional Loss SNV dbSNP153 33..33 33 - - - 60897 RMVar_ID_60897 Human_SNP_ID_565928478 m1A Human chr14 - 95157340 95157340 95157340 CAGCGGGGACGAGGCGACGGCGAGCGCGAGGAAATGGCGGCGGGGGCGGCGGCGCCGGGCGGCTC CAGCGGGGACGAGGCGACGGCGAGCGCGAGGACATGGCGGCGGGGGCGGCGGCGCCGGGCGGCTC T G DICER1 Ensembl:ENSG00000100697 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:95157297..95157512 26863196 MeRIP-seq:(Medium) rs886050946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231599,Human_RBP_ID_4306787,Human_RBP_ID_8725826,Human_RBP_ID_18418182 Clinvar_Rec_215 60898 RMVar_ID_60898 Human_SNP_ID_565928498 m1A Human chr14 - 95157392 95157392 95157392 GGCGGAGGCGCGGCGCAGGCTGCTGCAGGCCCAGGTGAATGGAGTAACCTGACAGCGGGGACGAG GGCGGAGGCGCGGCGCAGGCTGCTGCAGGCCCGGGTGAATGGAGTAACCTGACAGCGGGGACGAG T C DICER1 Ensembl:ENSG00000100697 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95157194..95157543 26863196 MeRIP-seq:(Medium) rs937855901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308076,Human_RBP_ID_8725826 Human_Splice_Rec_1550163 60899 RMVar_ID_60899 Human_SNP_ID_565928704 m1A Human chr14 - 95157831 95157831 95157831 GTTACGGTCTGTGGGTGCCAGAAGGAGCAACAATGGAGGCAGTCGAATTCCGAGAGCTCAGAGAG GTTACGGTCTGTGGGTGCCAGAAGGAGCAACAGTGGAGGCAGTCGAATTCCGAGAGCTCAGAGAG T C DICER1 Ensembl:ENSG00000100697 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:95157729..95157847 26863410 MeRIP-seq:(Medium) rs1170529592 Functional Loss SNV dbSNP153 33..33 33 - - - 60900 RMVar_ID_60900 Human_SNP_ID_565993759 m1A Human chr14 - 95419877 95419877 95419877 CTACCACCACCACCATCACTATCATCATCATCACCATCACCATCACCTCCATCACCATCATCACC CTACCACCACCACCATCACTATCATCATCATCGCCATCACCATCACCTCCATCACCATCATCACC T C SYNE3 Ensembl:ENSG00000176438 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95419841..95419906 26863196 MeRIP-seq:(Medium) rs1213505518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197261 60901 RMVar_ID_60901 Human_SNP_ID_565993770 m1A Human chr14 + 95419882 95419882 95419882 TGATGGTGATGGAGGTGATGGTGATGGTGATGATGATGATAGTGATGGTGGTGGTGGTAGTGATG TGATGGTGATGGAGGTGATGGTGATGGTGATGGTGATGATAGTGATGGTGGTGGTGGTAGTGATG A G NONHSAG015796.2 RNACentral:URS00008C09AE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:95419819..95419908 26863196 MeRIP-seq:(Medium) rs61981397 Functional Loss SNV dbSNP153 33..33 33 - - - 60902 RMVar_ID_60902 Human_SNP_ID_565993772 m1A Human chr14 - 95419883 95419883 95419883 CCATCACTACCACCACCACCATCACTATCATCATCATCACCATCACCATCACCTCCATCACCATC CCATCACTACCACCACCACCATCACTATCATCTTCATCACCATCACCATCACCTCCATCACCATC T A SYNE3 Ensembl:ENSG00000176438 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:95419831..95419915 26863196 MeRIP-seq:(Medium) rs891446883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197261 60903 RMVar_ID_60903 Human_SNP_ID_565993773 m1A Human chr14 - 95419883 95419883 95419883 CCATCACTACCACCACCACCATCACTATCATCATCATCACCATCACCATCACCTCCATCACCATC CCATCACTACCACCACCACCATCACTATCATCCTCATCACCATCACCATCACCTCCATCACCATC T G SYNE3 Ensembl:ENSG00000176438 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:95419831..95419915 26863196 MeRIP-seq:(Medium) rs891446883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197261 60904 RMVar_ID_60904 Human_SNP_ID_565999029 m1A Human chr14 - 95439675 95439674 95439675 GTCTTCTCCGGAGGGTGCTGCCGTGGTGCAGGAGGAGCTCAGGGAGCTGGCAGAGTCGTGGCGGG GTCTTCTCCGGAGGGTGCTGCCGTGGTGCAGG_GGAGCTCAGGGAGCTGGCAGAGTCGTGGCGGG CT C SYNE3 Ensembl:ENSG00000176438 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95439673..95439754 26863196 MeRIP-seq:(Medium) rs761656191 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1550377,Human_Splice_Rec_1550409,Human_Splice_Rec_1550433,Human_Splice_Rec_1550461 RMVar_hsa_circ_3108,RMVar_hsa_circ_19012,RMVar_hsa_circ_23334,RMVar_hsa_circ_269264,RMVar_hsa_circ_265939 60905 RMVar_ID_60905 Human_SNP_ID_566001705 m1A Human chr14 + 95449993 95449993 95449993 AGGCAGGTCCGGCAGGCTGGCAGTGACCTCCAAGAGCCGCTGGGCCAGGGCCTTCCACAGCTGCA AGGCAGGTCCGGCAGGCTGGCAGTGACCTCCAGGAGCCGCTGGGCCAGGGCCTTCCACAGCTGCA A G NONHSAG015796.2 RNACentral:URS00008C09AE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95449983..95450055 26863196 MeRIP-seq:(Medium) rs765452897 Functional Loss SNV dbSNP153 33..33 33 - - - 60906 RMVar_ID_60906 Human_SNP_ID_566003022 m1A Human chr14 - 95455424 95455424 95455424 GGCTGGCCCAGGAGGGCCTGCAGCCTGCGGCGAAAGCGGGGACCGAGGACGAGCTGGTGGCACAC GGCTGGCCCAGGAGGGCCTGCAGCCTGCGGCGGAAGCGGGGACCGAGGACGAGCTGGTGGCACAC T C SYNE3 Ensembl:ENSG00000176438 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95455349..95455651 26863196 MeRIP-seq:(Medium) rs1366168226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1550363,Human_Splice_Rec_1550395,Human_Splice_Rec_1550419,Human_Splice_Rec_1550449,Human_Splice_Rec_1550471 RMVar_hsa_circ_1241,RMVar_hsa_circ_3108,RMVar_hsa_circ_23334,RMVar_hsa_circ_47378,RMVar_hsa_circ_20576,RMVar_hsa_circ_93013,RMVar_hsa_circ_168851 60907 RMVar_ID_60907 Human_SNP_ID_566006430 m1A Human chr14 + 95467961 95467961 95467961 CACCCTCACACGCCCCTCGGGCTCCAGCTGGCATATTTTCTGTTGTGGACACACAAGCCAGTTTC CACCCTCACACGCCCCTCGGGCTCCAGCTGGCGTATTTTCTGTTGTGGACACACAAGCCAGTTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95467860..95468018 26863196 MeRIP-seq:(Medium) rs760607047 Functional Loss SNV dbSNP153 33..33 33 - - - 60908 RMVar_ID_60908 Human_SNP_ID_566008371 m1A Human chr14 + 95475640 95475640 95475640 CCTGAGGTCTGAGGGCGGGGTGGGATGGGGCCAAGACCACAGGGCCATCTGAGGCCACGCCTCTG CCTGAGGTCTGAGGGCGGGGTGGGATGGGGCCGAGACCACAGGGCCATCTGAGGCCACGCCTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95475636..95475797 26863196 MeRIP-seq:(Medium) rs373653788 Functional Loss SNV dbSNP153 33..33 33 - - - 60909 RMVar_ID_60909 Human_SNP_ID_566018362 m1A Human chr14 + 95516565 95516551 95516565 CGCCCGGCCCCCGGCCCCCGGCCCCCGGCCCCAGGCCTGGCCTCCCGGCCCCGTGCCACTTACCC CGCCCGGCCCCCGGCCCCC______________GGCCTGGCCTCCCGGCCCCGTGCCACTTACCC CGGCCCCCGGCCCCA C AL133467.1 Ensembl:ENSG00000258572 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95516555..95516651 26863196 MeRIP-seq:(Medium) rs1191503030 Functional Loss DEL dbSNP153 20..33 33 - - - 60910 RMVar_ID_60910 Human_SNP_ID_566018369 m1A Human chr14 + 95516565 95516558 95516565 CGCCCGGCCCCCGGCCCCCGGCCCCCGGCCCCAGGCCTGGCCTCCCGGCCCCGTGCCACTTACCC CGCCCGGCCCCCGGCCCCCGGCCCCC_______GGCCTGGCCTCCCGGCCCCGTGCCACTTACCC CGGCCCCA C AL133467.1 Ensembl:ENSG00000258572 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95516555..95516651 26863196 MeRIP-seq:(Medium) rs1389885442 Functional Loss DEL dbSNP153 27..33 33 - - - 60911 RMVar_ID_60911 Human_SNP_ID_566018373 m1A Human chr14 + 95516565 95516565 95516565 CGCCCGGCCCCCGGCCCCCGGCCCCCGGCCCCAGGCCTGGCCTCCCGGCCCCGTGCCACTTACCC CGCCCGGCCCCCGGCCCCCGGCCCCCGGCCCCCGGCCTGGCCTCCCGGCCCCGTGCCACTTACCC A C AL133467.1 Ensembl:ENSG00000258572 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95516555..95516651 26863196 MeRIP-seq:(Medium) rs1487367997 Functional Loss SNV dbSNP153 33..33 33 - - - 60912 RMVar_ID_60912 Human_SNP_ID_566023268 m1A Human chr14 + 95534574 95534574 95534574 GGCCTAGCCCCGCTACCTCCCAAGAGACCAACACGACAAGCGCGCGCCCACCGCATTGCCATGGC GGCCTAGCCCCGCTACCTCCCAAGAGACCAACGCGACAAGCGCGCGCCCACCGCATTGCCATGGC A G GLRX5 Ensembl:ENSG00000182512 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95534482..95534585 26863196 MeRIP-seq:(Medium) rs1396297160 Functional Loss SNV dbSNP153 33..33 33 - - - 60913 RMVar_ID_60913 Human_SNP_ID_566023576 m1A Human chr14 - 95535189 95535189 95535189 CTGCTCCGCCGAGCCGCCGCCGCCCGCGCCCGAGCCCGCCGCCCGCACGCCCGGACCCCAAAGGC CTGCTCCGCCGAGCCGCCGCCGCCCGCGCCCGGGCCCGCCGCCCGCACGCCCGGACCCCAAAGGC T C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control chr14:95535089..95535240;chr14:95535089..95535244;chr14:95535089..95535237 26863410 MeRIP-seq:(Medium) rs1328178162 Functional Loss SNV dbSNP153 33..33 33 - - - 60914 RMVar_ID_60914 Human_SNP_ID_566023598 m1A Human chr14 + 95535226 95535226 95535226 CGCGGGCGGCGGCGGCTCGGCGGAGCAGTTGGACGCGCTGGTGAAGAAGGACAAGGTGGTGGTCT CGCGGGCGGCGGCGGCTCGGCGGAGCAGTTGGGCGCGCTGGTGAAGAAGGACAAGGTGGTGGTCT A G GLRX5 Ensembl:ENSG00000182512 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:95535138..95535228 26863410 MeRIP-seq:(Medium) rs1213705441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1501701,Human_RBP_ID_1826632,Human_RBP_ID_4308488,Human_RBP_ID_5112592,Human_RBP_ID_6398516,Human_RBP_ID_8941063,Human_RBP_ID_9323842,Human_RBP_ID_17117214,Human_RBP_ID_17651451,Human_RBP_ID_17687835,Human_RBP_ID_26929253 60915 RMVar_ID_60915 Human_SNP_ID_566023607 m1A Human chr14 + 95535240 95535240 95535240 GCTCGGCGGAGCAGTTGGACGCGCTGGTGAAGAAGGACAAGGTGGTGGTCTTCCTCAAGGGGACG GCTCGGCGGAGCAGTTGGACGCGCTGGTGAAGGAGGACAAGGTGGTGGTCTTCCTCAAGGGGACG A G GLRX5 Ensembl:ENSG00000182512 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:95535139..95535240 32194978 MeRIP-seq:(Medium) rs747458426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_999952,Human_RBP_ID_1501701,Human_RBP_ID_1826632,Human_RBP_ID_3466610,Human_RBP_ID_4308488,Human_RBP_ID_5112592,Human_RBP_ID_6398516,Human_RBP_ID_8941063,Human_RBP_ID_9047730,Human_RBP_ID_9323842,Human_RBP_ID_17117214,Human_RBP_ID_17651451,Human_RBP_ID_17687835,Human_RBP_ID_18659377,Human_RBP_ID_22439428,Human_RBP_ID_26929253 60916 RMVar_ID_60916 Human_SNP_ID_566023657 m1A Human chr14 - 95535325 95535325 95535325 CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCAGCCGCAGGATCTGCACCACGGCGTTGCTGAAG CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCTGCCGCAGGATCTGCACCACGGCGTTGCTGAAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:95535276..95543028 32194978 MeRIP-seq:(Medium) rs752203652 Functional Loss SNV dbSNP153 33..33 33 - - - 60917 RMVar_ID_60917 Human_SNP_ID_566023658 m1A Human chr14 - 95535325 95535325 95535325 CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCAGCCGCAGGATCTGCACCACGGCGTTGCTGAAG CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCGGCCGCAGGATCTGCACCACGGCGTTGCTGAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:95535276..95543028 32194978 MeRIP-seq:(Medium) rs752203652 Functional Loss SNV dbSNP153 33..33 33 - - - 60918 RMVar_ID_60918 Human_SNP_ID_566023659 m1A Human chr14 - 95535325 95535325 95535325 CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCAGCCGCAGGATCTGCACCACGGCGTTGCTGAAG CGTTGTAGGCCGCGTAATCGCGGACGCCGTGCCGCCGCAGGATCTGCACCACGGCGTTGCTGAAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:95535276..95543028 32194978 MeRIP-seq:(Medium) rs752203652 Functional Loss SNV dbSNP153 33..33 33 - - - 60919 RMVar_ID_60919 Human_SNP_ID_566023669 m1A Human chr14 + 95535340 95535340 95535340 GGTGCAGATCCTGCGGCTGCACGGCGTCCGCGATTACGCGGCCTACAACGTGCTGGACGACCCGG GGTGCAGATCCTGCGGCTGCACGGCGTCCGCGGTTACGCGGCCTACAACGTGCTGGACGACCCGG A G GLRX5 Ensembl:ENSG00000182512 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:95535089..95535340 32194978 MeRIP-seq:(Medium) rs375487410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231799,Human_RBP_ID_454180,Human_RBP_ID_999954,Human_RBP_ID_1826633,Human_RBP_ID_6398519 Human_Splice_Rec_1550509,Human_Splice_Rec_1550511 60920 RMVar_ID_60920 Human_SNP_ID_566046734 m1A Human chr14 + 95625529 95625529 95625529 AAGGTTCTAAGAGGAGAGAGGAAAGAAGTGGCAAGGAGAAGGTGGACAAGCATGCTGGGGAGGCA AAGGTTCTAAGAGGAGAGAGGAAAGAAGTGGCGAGGAGAAGGTGGACAAGCATGCTGGGGAGGCA A G AL133467.2 Ensembl:ENSG00000258927 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:95625432..95625737 26863196 MeRIP-seq:(Medium) rs930954754 Functional Loss SNV dbSNP153 33..33 33 - - - 60921 RMVar_ID_60921 Human_SNP_ID_566051270 m1A Human chr14 - 95645623 95645623 95645623 CTGTGCTCACCTCTGCACTTGAACTCACCCCAATGCCCACACCTGGAACGACCTCGTGTTCATCC CTGTGCTCACCTCTGCACTTGAACTCACCCCAGTGCCCACACCTGGAACGACCTCGTGTTCATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:95645475..95645643 26863196 MeRIP-seq:(Medium) rs548810725 Functional Loss SNV dbSNP153 33..33 33 - - - 60922 RMVar_ID_60922 Human_SNP_ID_566212364 m1A Human chr14 - 96282273 96282273 96282273 ACAAAGCAATATTCTTTTGTATCTGCAAATGCATCAGCTGGACATACCAATTGGTATCAAATAGA ACAAAGCAATATTCTTTTGTATCTGCAAATGCGTCAGCTGGACATACCAATTGGTATCAAATAGA T C ATG2B Ensembl:ENSG00000066739 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7150634 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7370,GWAS_ID_7371,GWAS_ID_7372,GWAS_ID_7373,GWAS_ID_7374,GWAS_ID_7375,GWAS_ID_7376,GWAS_ID_7377,GWAS_ID_7378,GWAS_ID_7379,GWAS_ID_7380,GWAS_ID_7381,GWAS_ID_7382,GWAS_ID_7383,GWAS_ID_7384,GWAS_ID_7385,GWAS_ID_7386,GWAS_ID_7387 RMVar_hsa_circ_90457,RMVar_hsa_circ_268876,RMVar_hsa_circ_168857 60923 RMVar_ID_60923 Human_SNP_ID_566233161 m1A Human chr14 - 96364203 96364200 96364204 CACCCGCACCCAGGCCTTTCGAGGTTGACTTAACTTAACAGCCGGCTCCGCCTCTGCAGGAGTTA CACCCGCACCCAGGCCTTTCGAGGTTGACTT____TAACAGCCGGCTCCGCCTCTGCAGGAGTTA AAGTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:96364191..96364381 26863196 MeRIP-seq:(Medium) rs1483934922 Functional Loss DEL dbSNP153 32..35 33 - - - 60924 RMVar_ID_60924 Human_SNP_ID_566267322 m1A Human chr14 - 96502080 96502080 96502080 GAGGCACCGCTTCCGGCGCATTGTGAGGTCCCACCTTTCCCGCCGCCTGAGGTCGCGGCGGCTGC GAGGCACCGCTTCCGGCGCATTGTGAGGTCCCTCCTTTCCCGCCGCCTGAGGTCGCGGCGGCTGC T A AL163051.1 Ensembl:ENSG00000260806 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:96501979..96502126 26863410 MeRIP-seq:(Medium) rs1305620469 Functional Loss SNV dbSNP153 33..33 33 - - - 60925 RMVar_ID_60925 Human_SNP_ID_566267501 m1A Human chr14 + 96502470 96502459 96502470 AAGCGCTTAAAGCGGCGGGAGCGGTGCGGGAGAGGGGTTGGACCCAGGGCTGAGGCAGGCCCCCC AAGCGCTTAAAGCGGCGGGAGC___________GGGGTTGGACCCAGGGCTGAGGCAGGCCCCCC CGGTGCGGGAGA C PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:96502401..96502625 26863196 MeRIP-seq:(Medium) rs1316922336 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_231523,Human_RBP_ID_454294,Human_RBP_ID_812951,Human_RBP_ID_4308084,Human_RBP_ID_5112593,Human_RBP_ID_6399082,Human_RBP_ID_18418027,Human_RBP_ID_22355354,Human_RBP_ID_22926234,Human_RBP_ID_26325366 60926 RMVar_ID_60926 Human_SNP_ID_566267511 m1A Human chr14 - 96502475 96502475 96502475 GGAGGGGGGGGCCTGCCTCAGCCCTGGGTCCAACCCCTCTCCCGCACCGCTCCCGCCGCTTTAAG GGAGGGGGGGGCCTGCCTCAGCCCTGGGTCCAGCCCCTCTCCCGCACCGCTCCCGCCGCTTTAAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:96502426..96502600 26863196 MeRIP-seq:(Medium) rs1015892558 Functional Loss SNV dbSNP153 33..33 33 - - - 60927 RMVar_ID_60927 Human_SNP_ID_566267512 m1A Human chr14 - 96502475 96502475 96502475 GGAGGGGGGGGCCTGCCTCAGCCCTGGGTCCAACCCCTCTCCCGCACCGCTCCCGCCGCTTTAAG GGAGGGGGGGGCCTGCCTCAGCCCTGGGTCCACCCCCTCTCCCGCACCGCTCCCGCCGCTTTAAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:96502426..96502600 26863196 MeRIP-seq:(Medium) rs1015892558 Functional Loss SNV dbSNP153 33..33 33 - - - 60928 RMVar_ID_60928 Human_SNP_ID_566267602 m1A Human chr14 - 96502576 96502576 96502576 TTACTTACAACGGCATCGTCTCCGGCGCCGGCACCGCCCAGTCACTTCCCCCCCGCAACCGCCGC TTACTTACAACGGCATCGTCTCCGGCGCCGGCGCCGCCCAGTCACTTCCCCCCCGCAACCGCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:96502476..96502642 26863410 MeRIP-seq:(Medium) rs776518436 Functional Loss SNV dbSNP153 33..33 33 - - - 60929 RMVar_ID_60929 Human_SNP_ID_566272387 m1A Human chr14 - 96519996 96519996 96519996 TGCCAAAAGAATTCTACAATTTGAAACAAATCAGTAAGACCAGAAAAACTAATTTAGTAACACAC TGCCAAAAGAATTCTACAATTTGAAACAAATCGGTAAGACCAGAAAAACTAATTTAGTAACACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:96519994..96520100 26863196 MeRIP-seq:(Medium) rs1390663116 Functional Loss SNV dbSNP153 33..33 33 - - - 60930 RMVar_ID_60930 Human_SNP_ID_566280575 m1A Human chr14 - 96552617 96552617 96552617 CACTTCTATTTCCCTCTTTTTCCTTACCCCTGAGAGCTGCCAGAACTGTTCAATGGACTGGTCTT CACTTCTATTTCCCTCTTTTTCCTTACCCCTGGGAGCTGCCAGAACTGTTCAATGGACTGGTCTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:96552571..96552659 32194978 MeRIP-seq:(Medium) rs765584595 Functional Loss SNV dbSNP153 33..33 33 - - - 60931 RMVar_ID_60931 Human_SNP_ID_566341016 m1A Human chr14 + 96797445 96797445 96797445 GTACTGGGCAGAACGCGACGGGTCTGCGGCTTAGGGTAGGGAGGCCGCAGGCGACACGGCTCGAG GTACTGGGCAGAACGCGACGGGTCTGCGGCTTGGGGTAGGGAGGCCGCAGGCGACACGGCTCGAG A G VRK1 Ensembl:ENSG00000100749 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:96797418..96797504;chr14:96797419..96797529 26863196 MeRIP-seq:(Medium) rs916047691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756892,Human_RBP_ID_5353311,Human_RBP_ID_6399991,Human_RBP_ID_9323845,Human_RBP_ID_19065961,Human_RBP_ID_23208761 Human_Splice_Rec_1551557,Human_Splice_Rec_1551581 RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_168922 60932 RMVar_ID_60932 Human_SNP_ID_566341017 m1A Human chr14 + 96797445 96797445 96797445 GTACTGGGCAGAACGCGACGGGTCTGCGGCTTAGGGTAGGGAGGCCGCAGGCGACACGGCTCGAG GTACTGGGCAGAACGCGACGGGTCTGCGGCTTTGGGTAGGGAGGCCGCAGGCGACACGGCTCGAG A T VRK1 Ensembl:ENSG00000100749 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:96797418..96797504;chr14:96797419..96797529 26863196 MeRIP-seq:(Medium) rs916047691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756892,Human_RBP_ID_5353311,Human_RBP_ID_6399991,Human_RBP_ID_9323845,Human_RBP_ID_19065961,Human_RBP_ID_23208761 Human_Splice_Rec_1551557,Human_Splice_Rec_1551581 RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_168922 60933 RMVar_ID_60933 Human_SNP_ID_566349414 m1A Human chr14 + 96833516 96833516 96833516 AAAGCAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGAGACATCTTGCAGAACAATTTGCAGTTGG AAAGCAGCTCAAGCTGGAAGACAGAGCTCTGCGAAGAGACATCTTGCAGAACAATTTGCAGTTGG A G VRK1 Ensembl:ENSG00000100749 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2145635 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17856051 Human_Splice_Rec_1551558,Human_Splice_Rec_1551582 Clinvar_Rec_216 GWAS_ID_7388,GWAS_ID_7389,GWAS_ID_7390,GWAS_ID_7391,GWAS_ID_7392,GWAS_ID_7393,GWAS_ID_7394,GWAS_ID_7395,GWAS_ID_7396,GWAS_ID_7397,GWAS_ID_7398,GWAS_ID_7399,GWAS_ID_7400,GWAS_ID_7401 RMVar_hsa_circ_116596,RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_309331,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_361287,RMVar_hsa_circ_168922,RMVar_hsa_circ_323937,RMVar_hsa_circ_271676,RMVar_hsa_circ_300344,RMVar_hsa_circ_269902,RMVar_hsa_circ_168926,RMVar_hsa_circ_168928,RMVar_hsa_circ_13272,RMVar_hsa_circ_168929,RMVar_hsa_circ_168927,RMVar_hsa_circ_168925 60934 RMVar_ID_60934 Human_SNP_ID_566349418 m1A Human chr14 - 96833525 96833525 96833525 ATTATCTCTCCAACTGCAAATTGTTCTGCAAGATGTCTCTTTGCAGAGCTCTGTCTTCCAGCTTG ATTATCTCTCCAACTGCAAATTGTTCTGCAAGTTGTCTCTTTGCAGAGCTCTGTCTTCCAGCTTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:96833475..96833560 26863196 MeRIP-seq:(Medium) rs1379251732 Functional Loss SNV dbSNP153 33..33 33 - - - 60935 RMVar_ID_60935 Human_SNP_ID_566349419 m1A Human chr14 - 96833525 96833525 96833525 ATTATCTCTCCAACTGCAAATTGTTCTGCAAGATGTCTCTTTGCAGAGCTCTGTCTTCCAGCTTG ATTATCTCTCCAACTGCAAATTGTTCTGCAAGCTGTCTCTTTGCAGAGCTCTGTCTTCCAGCTTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:96833475..96833560 26863196 MeRIP-seq:(Medium) rs1379251732 Functional Loss SNV dbSNP153 33..33 33 - - - 60936 RMVar_ID_60936 Human_SNP_ID_566974887 m1A Human chr14 - 99173148 99173148 99173148 AGATGGGGTGGCCTGCAGTGACACAGAAAGGAAGAAACTAGCGGTGTTCTTTTAGGCGTTTTCTG AGATGGGGTGGCCTGCAGTGACACAGAAAGGAGGAAACTAGCGGTGTTCTTTTAGGCGTTTTCTG T C BCL11B Ensembl:ENSG00000127152 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:99173125..99173207 26863410 MeRIP-seq:(Medium) rs1236044120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6401861 RMVar_hsa_circ_168951 60937 RMVar_ID_60937 Human_SNP_ID_567038859 m1A Human chr14 - 99420977 99420966 99420977 AAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC AAGAAGACAGCAGTAGCTTGTCTGCACCTCCC___________CCCCCCCCCCCCCCCCCCCGCC GGGGGGGGGGGT G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr14:99420852..99421000;chr14:99420926..99421000;chr14:99420867..99421055 26863196 MeRIP-seq:(Medium) rs1566694362 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60938 RMVar_ID_60938 Human_SNP_ID_567038872 m1A Human chr14 - 99420977 99420974 99420977 AAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC AAGAAGACAGCAGTAGCTTGTCTGCACCTCCC___CCCCCCCCCCCCCCCCCCCCCCCCCCCGCC GGGT G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr14:99420852..99421000;chr14:99420926..99421000;chr14:99420867..99421055 26863196 MeRIP-seq:(Medium) rs1566694390 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60939 RMVar_ID_60939 Human_SNP_ID_567038875 m1A Human chr14 - 99420977 99420976 99420977 AAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC AAGAAGACAGCAGTAGCTTGTCTGCACCTCCC_CCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC GT G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr14:99420852..99421000;chr14:99420926..99421000;chr14:99420867..99421055 26863196 MeRIP-seq:(Medium) rs1566694399 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60940 RMVar_ID_60940 Human_SNP_ID_567038877 m1A Human chr14 - 99420984 99420976 99420984 GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCC GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGC________CCCCCCCCCCCCCCCCCCCCCCCCC GTGGGAGGT G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr14:99420915..99420993;chr14:99420851..99421000 26863196 MeRIP-seq:(Medium) rs1566694419 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60941 RMVar_ID_60941 Human_SNP_ID_567038878 m1A Human chr14 - 99420977 99420977 99420977 AAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC AAGAAGACAGCAGTAGCTTGTCTGCACCTCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCC T G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr14:99420852..99421000;chr14:99420926..99421000;chr14:99420867..99421055 26863196 MeRIP-seq:(Medium) rs867046649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60942 RMVar_ID_60942 Human_SNP_ID_567038889 m1A Human chr14 - 99420984 99420980 99420984 GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCC GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGC____CCCACCCCCCCCCCCCCCCCCCCCCCCCC GAGGT G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr14:99420915..99420993;chr14:99420851..99421000 26863196 MeRIP-seq:(Medium) rs1566694444 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60943 RMVar_ID_60943 Human_SNP_ID_567038895 m1A Human chr14 - 99420984 99420984 99420984 GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGCACCTCCCACCCCCCCCCCCCCCCCCCCCCCCCC GTCTTTAAAGAAGACAGCAGTAGCTTGTCTGCCCCTCCCACCCCCCCCCCCCCCCCCCCCCCCCC T G SETD3 Ensembl:ENSG00000183576 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr14:99420915..99420993;chr14:99420851..99421000 26863196 MeRIP-seq:(Medium) rs1202873282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116345,RMVar_hsa_circ_300828,RMVar_hsa_circ_361790,RMVar_hsa_circ_93655,RMVar_hsa_circ_168959,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_168961,RMVar_hsa_circ_373326,RMVar_hsa_circ_168963 60944 RMVar_ID_60944 Human_SNP_ID_567049232 m1A Human chr14 - 99463553 99463553 99463553 GTTACAGAATGCAGCAGTCCGGCGCCTGGCCCAGGAAAAGAGTGGGAAGAGTATGTGCAGATCCG GTTACAGAATGCAGCAGTCCGGCGCCTGGCCCGGGAAAAGAGTGGGAAGAGTATGTGCAGATCCG T C SETD3 Ensembl:ENSG00000183576 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:99459181..99465707 32194978 MeRIP-seq:(Medium) rs1366863916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_454589,Human_RBP_ID_882205,Human_RBP_ID_6402282,Human_RBP_ID_23643838 Human_Splice_Rec_1551866,Human_Splice_Rec_1551867,Human_Splice_Rec_1551890,Human_Splice_Rec_1551891,Human_Splice_Rec_1551912,Human_Splice_Rec_1551913,Human_Splice_Rec_1551928,Human_Splice_Rec_1551929,Human_Splice_Rec_1551944,Human_Splice_Rec_1551945,Human_Splice_Rec_1551958,Human_Splice_Rec_1551959,Human_Splice_Rec_1551972,Human_Splice_Rec_1551973,Human_Splice_Rec_1551984,Human_Splice_Rec_1551985 Human_miRNA_ID_2040568,Human_miRNA_ID_2040569,Human_miRNA_ID_2662712,Human_miRNA_ID_2662713,Human_miRNA_ID_2681163,Human_miRNA_ID_2681164,Human_miRNA_ID_3019549,Human_miRNA_ID_3019550 RMVar_hsa_circ_116345,RMVar_hsa_circ_168960,RMVar_hsa_circ_360917,RMVar_hsa_circ_324648,RMVar_hsa_circ_274216,RMVar_hsa_circ_320260,RMVar_hsa_circ_168965,RMVar_hsa_circ_168966,RMVar_hsa_circ_9935,RMVar_hsa_circ_168968 60945 RMVar_ID_60945 Human_SNP_ID_567054015 m1A Human chr14 - 99481481 99481481 99481481 GGGCGGCGCTGCCCTCAGTCGGTGGGTCACTCACCCCTCGCTTCAGGCAAGCCCCTCAGCGACGT GGGCGGCGCTGCCCTCAGTCGGTGGGTCACTCTCCCCTCGCTTCAGGCAAGCCCCTCAGCGACGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:99481454..99481570;chr14:99481453..99481556 26863196 MeRIP-seq:(Medium) rs945144539 Functional Loss SNV dbSNP153 33..33 33 - - - 60946 RMVar_ID_60946 Human_SNP_ID_567060323 m1A Human chr14 + 99507119 99507119 99507119 CCTAAAATCCCCAAAATTGAGACCACTCATCCACCGTTGCCTCCAGCCCACCCACCTCCAGGTAA CCTAAAATCCCCAAAATTGAGACCACTCATCCGCCGTTGCCTCCAGCCCACCCACCTCCAGGTAA A G CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:99503640..99510750;chr14:99503640..99510440;chr14:99503640..99510281 26863196 MeRIP-seq:(Medium) rs1452854368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5127720,Human_RBP_ID_17248640,Human_RBP_ID_17363391,Human_RBP_ID_18937598,Human_RBP_ID_19065974,Human_RBP_ID_22649229 Human_Splice_Rec_1552018,Human_Splice_Rec_1552019,Human_Splice_Rec_1552052,Human_Splice_Rec_1552053,Human_Splice_Rec_1552078,Human_Splice_Rec_1552079 60947 RMVar_ID_60947 Human_SNP_ID_567061076 m1A Human chr14 + 99510107 99510107 99510107 GATGGCCCTGAAGGGCCAGGAGGCACTGAAAAAGCAACCATTGCTGGCGGAGGCCGGGCACTGAT GATGGCCCTGAAGGGCCAGGAGGCACTGAAAAGGCAACCATTGCTGGCGGAGGCCGGGCACTGAT A G CCNK Ensembl:ENSG00000090061 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:99510102..99510310 26863196 MeRIP-seq:(Medium) rs748456006 Functional Loss SNV dbSNP153 33..33 33 - - - 60948 RMVar_ID_60948 Human_SNP_ID_567061077 m1A Human chr14 + 99510107 99510107 99510107 GATGGCCCTGAAGGGCCAGGAGGCACTGAAAAAGCAACCATTGCTGGCGGAGGCCGGGCACTGAT GATGGCCCTGAAGGGCCAGGAGGCACTGAAAATGCAACCATTGCTGGCGGAGGCCGGGCACTGAT A T CCNK Ensembl:ENSG00000090061 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:99510102..99510310 26863196 MeRIP-seq:(Medium) rs748456006 Functional Loss SNV dbSNP153 33..33 33 - - - 60949 RMVar_ID_60949 Human_SNP_ID_567061168 m1A Human chr14 + 99510274 99510274 99510274 TCCCCCTCCGGCCCACCCGGCCCCTGTGCACCAGCCACCGCCGCTGCCACACCGGCCCCCGCCCC TCCCCCTCCGGCCCACCCGGCCCCTGTGCACCTGCCACCGCCGCTGCCACACCGGCCCCCGCCCC A T CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:99510268..99510498 26863196 MeRIP-seq:(Medium) rs1459139101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_454602,Human_RBP_ID_812920,Human_RBP_ID_17363393 60950 RMVar_ID_60950 Human_SNP_ID_567061190 m1A Human chr14 + 99510308 99510305 99510308 CCACCGCCGCTGCCACACCGGCCCCCGCCCCCACCCCCCTCCAGCTACATGACCGGGATGTCCAC CCACCGCCGCTGCCACACCGGCCCCCGCCC___CCCCCCTCCAGCTACATGACCGGGATGTCCAC CCCA C CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:99510178..99510379 32194978 MeRIP-seq:(Medium) rs1291327922 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_454603,Human_RBP_ID_17363393 Human_miRNA_ID_464312,Human_miRNA_ID_1559617 60951 RMVar_ID_60951 Human_SNP_ID_567061195 m1A Human chr14 + 99510308 99510308 99510308 CCACCGCCGCTGCCACACCGGCCCCCGCCCCCACCCCCCTCCAGCTACATGACCGGGATGTCCAC CCACCGCCGCTGCCACACCGGCCCCCGCCCCCCCCCCCCTCCAGCTACATGACCGGGATGTCCAC A C CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:99510178..99510379 32194978 MeRIP-seq:(Medium) rs745936510 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_454603,Human_RBP_ID_17363393 Human_miRNA_ID_464312,Human_miRNA_ID_1559617 60952 RMVar_ID_60952 Human_SNP_ID_567061209 m1A Human chr14 + 99510318 99510318 99510318 TGCCACACCGGCCCCCGCCCCCACCCCCCTCCAGCTACATGACCGGGATGTCCACCACCAGCTCC TGCCACACCGGCCCCCGCCCCCACCCCCCTCCCGCTACATGACCGGGATGTCCACCACCAGCTCC A C CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:99510218..99510458 26863410 MeRIP-seq:(Medium) rs772955703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_454603,Human_RBP_ID_26808602 60953 RMVar_ID_60953 Human_SNP_ID_567061416 m1A Human chr14 + 99510877 99510877 99510877 TGAAGTGGGTAAGCAGCAGGGTACCTTGTATAATGCACGACAGTTGCAGTATGGGAAGAATGGAC TGAAGTGGGTAAGCAGCAGGGTACCTTGTATAGTGCACGACAGTTGCAGTATGGGAAGAATGGAC A G CCNK Ensembl:ENSG00000090061 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:99510828..99510964 26863196 MeRIP-seq:(Medium) rs1160779159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758089,Human_RBP_ID_3467728,Human_RBP_ID_5127616,Human_RBP_ID_12460105,Human_RBP_ID_17481003,Human_RBP_ID_18937604,Human_RBP_ID_23643933 Human_miRNA_ID_979248,Human_miRNA_ID_983980 60954 RMVar_ID_60954 Human_SNP_ID_567062992 m1A Human chr14 + 99516285 99516268 99516286 GCTGCCGGTCCAGATTCTCGTGTACCTCCAGGACCTGAAGGGAACGGGTCTCGGGGTCAGGGGCA GCTGCCGGTCCAGATT__________________CTGAAGGGAACGGGTCTCGGGGTCAGGGGCA TCTCGTGTACCTCCAGGAC T CCNK Ensembl:ENSG00000090061 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:99516279..99522180;chr14:99516279..99522230 26863196 MeRIP-seq:(Medium) rs1360391592 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_8413787 60955 RMVar_ID_60955 Human_SNP_ID_567078863 m1A Human chr14 - 99577665 99577665 99577665 CACACACACACACACACACTGATGGGGGATGCAGGACGGGCTGTATGGGCATGGATACATGCACA CACACACACACACACACACTGATGGGGGATGCGGGACGGGCTGTATGGGCATGGATACATGCACA T C CCDC85C Ensembl:ENSG00000205476 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:99577662..99577795 26863196 MeRIP-seq:(Medium) rs999879325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9417834,Human_RBP_ID_17844325 60956 RMVar_ID_60956 Human_SNP_ID_567085324 m1A Human chr14 + 99603212 99603212 99603212 GGGGATGCTGCGGTGGTGCGGCGGCGCCGACAAGTCGTCCAGGGACCGACGTGTGGCTCCTGCCT GGGGATGCTGCGGTGGTGCGGCGGCGCCGACAGGTCGTCCAGGGACCGACGTGTGGCTCCTGCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:99603175..99603976 32194978 MeRIP-seq:(Medium) rs1244814067 Functional Loss SNV dbSNP153 33..33 33 - - - 60957 RMVar_ID_60957 Human_SNP_ID_567085350 m1A Human chr14 - 99603288 99603288 99603288 GGCGGCAGCCCCGACCACCACCACCACGTCCCACCCCCGCTGCTGCCCCCCGGGCCGCACAAGGC GGCGGCAGCCCCGACCACCACCACCACGTCCCCCCCCCGCTGCTGCCCCCCGGGCCGCACAAGGC T G CCDC85C Ensembl:ENSG00000205476 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:99603188..99603390 26863410 MeRIP-seq:(Medium) rs1026600431 Functional Loss SNV dbSNP153 33..33 33 - - - 60958 RMVar_ID_60958 Human_SNP_ID_567085569 m1A Human chr14 - 99603824 99603824 99603824 TGCGGCGCGCCGAGGGCGAGAAGGTGGGCCTCATGCTGGAGCACGGCGGCCTGATGCGCGACGTG TGCGGCGCGCCGAGGGCGAGAAGGTGGGCCTCTTGCTGGAGCACGGCGGCCTGATGCGCGACGTG T A CCDC85C Ensembl:ENSG00000205476 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:99603801..99604187 26863196 MeRIP-seq:(Medium) rs763434759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4280344 60959 RMVar_ID_60959 Human_SNP_ID_567085570 m1A Human chr14 - 99603824 99603824 99603824 TGCGGCGCGCCGAGGGCGAGAAGGTGGGCCTCATGCTGGAGCACGGCGGCCTGATGCGCGACGTG TGCGGCGCGCCGAGGGCGAGAAGGTGGGCCTCCTGCTGGAGCACGGCGGCCTGATGCGCGACGTG T G CCDC85C Ensembl:ENSG00000205476 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:99603801..99604187 26863196 MeRIP-seq:(Medium) rs763434759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4280344 60960 RMVar_ID_60960 Human_SNP_ID_567085577 m1A Human chr14 - 99603844 99603844 99603844 GGAGGAGCTGGCGCGGCGGCTGCGGCGCGCCGAGGGCGAGAAGGTGGGCCTCATGCTGGAGCACG GGAGGAGCTGGCGCGGCGGCTGCGGCGCGCCGCGGGCGAGAAGGTGGGCCTCATGCTGGAGCACG T G CCDC85C Ensembl:ENSG00000205476 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:99603826..99604078 26863196 MeRIP-seq:(Medium) rs1482639215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308090,Human_RBP_ID_22438910 60961 RMVar_ID_60961 Human_SNP_ID_567085712 m1A Human chr14 - 99604166 99604166 99604166 AGAGCGCCCGGCACCGCGGCCGCCGACGCAGCAGCCGCCTCCGCTCGTCAACCCCGAGGCGCGCG AGAGCGCCCGGCACCGCGGCCGCCGACGCAGCGGCCGCCTCCGCTCGTCAACCCCGAGGCGCGCG T C CCDC85C Ensembl:ENSG00000205476 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:99603876..99604200 26863410 MeRIP-seq:(Medium) rs1304615743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4280354 60962 RMVar_ID_60962 Human_SNP_ID_567134939 m1A Human chr14 + 99793484 99793484 99793484 GCGGGCGCGGCCCGGCGGCCTCAGCATGGAGGACGGCTTCTCCAGCTACAGCAGCCTGTACGACA GCGGGCGCGGCCCGGCGGCCTCAGCATGGAGGGCGGCTTCTCCAGCTACAGCAGCCTGTACGACA A G EML1 Ensembl:ENSG00000066629 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:99793435..99793536 32194978 MeRIP-seq:(Medium) rs1188512269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1552421,Human_Splice_Rec_1552465,Human_Splice_Rec_1552471,Human_Splice_Rec_1552513 RMVar_hsa_circ_110014,RMVar_hsa_circ_168973 60963 RMVar_ID_60963 Human_SNP_ID_567148587 m1A Human chr14 + 99850897 99850897 99850897 CTGCTGCAAGTAGCATGGAGGTGACAGACCGCATTGCTTCACTGGAGCAGAGAGTCCAGATGCAA CTGCTGCAAGTAGCATGGAGGTGACAGACCGCGTTGCTTCACTGGAGCAGAGAGTCCAGATGCAA A G EML1 Ensembl:ENSG00000066629 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:99850808..99850896 26863196 MeRIP-seq:(Medium) rs376349469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1487341 Human_Splice_Rec_1552294,Human_Splice_Rec_1552314,Human_Splice_Rec_1552322,Human_Splice_Rec_1552366,Human_Splice_Rec_1552372,Human_Splice_Rec_1552416,Human_Splice_Rec_1552422,Human_Splice_Rec_1552466,Human_Splice_Rec_1552472,Human_Splice_Rec_1552514,Human_Splice_Rec_1552530,Human_Splice_Rec_1552536 RMVar_hsa_circ_168977,RMVar_hsa_circ_110014,RMVar_hsa_circ_168974,RMVar_hsa_circ_168973,RMVar_hsa_circ_168975,RMVar_hsa_circ_31947,RMVar_hsa_circ_13783,RMVar_hsa_circ_277283,RMVar_hsa_circ_307494,RMVar_hsa_circ_168976,RMVar_hsa_circ_331986,RMVar_hsa_circ_279906,RMVar_hsa_circ_265741,RMVar_hsa_circ_168978,RMVar_hsa_circ_168980,RMVar_hsa_circ_168981,RMVar_hsa_circ_168979 60964 RMVar_ID_60964 Human_SNP_ID_567202121 m1A Human chr14 - 100068621 100068621 100068621 ACCACGGCACTTCCTGAATCTGGTGACTTCTCACCGCCTACCCTGACTGCTCCACTGCTGGCCCA ACCACGGCACTTCCTGAATCTGGTGACTTCTCGCCGCCTACCCTGACTGCTCCACTGCTGGCCCA T C AL157912.1 Ensembl:ENSG00000258560 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100068615..100068780 26863196 MeRIP-seq:(Medium) rs1190964 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7402 60965 RMVar_ID_60965 Human_SNP_ID_567206053 m1A Human chr14 + 100084630 100084630 100084630 GTAGCAATTGGCCTCTATTTCAGAAAAGGGCAAAGTCAACTTCCATCCACTGTAGCTGAGGCTGA GTAGCAATTGGCCTCTATTTCAGAAAAGGGCAGAGTCAACTTCCATCCACTGTAGCTGAGGCTGA A G EVL Ensembl:ENSG00000196405 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:100084628..100084750 26863196 MeRIP-seq:(Medium) rs540535162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333688 60966 RMVar_ID_60966 Human_SNP_ID_567216560 m1A Human chr14 + 100126756 100126756 100126756 ACCAGCAGCAGCGTCAGGAATCTCTAGAAAGAAGAACCTCGGCCACAGGTGAGAGCCCTCCTCCC ACCAGCAGCAGCGTCAGGAATCTCTAGAAAGAGGAACCTCGGCCACAGGTGAGAGCCCTCCTCCC A G EVL Ensembl:ENSG00000196405 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:100114585..100128633 32194978 MeRIP-seq:(Medium) rs756579670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944645,Human_RBP_ID_9370415,Human_RBP_ID_18644569 Human_Splice_Rec_1552618,Human_Splice_Rec_1552619,Human_Splice_Rec_1552644,Human_Splice_Rec_1552645,Human_Splice_Rec_1552688,Human_Splice_Rec_1552689,Human_Splice_Rec_1552722,Human_Splice_Rec_1552723,Human_Splice_Rec_1552730,Human_Splice_Rec_1552731,Human_Splice_Rec_1552760,Human_Splice_Rec_1552761,Human_Splice_Rec_1552772,Human_Splice_Rec_1552773,Human_Splice_Rec_1552784,Human_Splice_Rec_1552785 RMVar_hsa_circ_89358,RMVar_hsa_circ_6840,RMVar_hsa_circ_169017,RMVar_hsa_circ_100284,RMVar_hsa_circ_169019 60967 RMVar_ID_60967 Human_SNP_ID_567217148 m1A Human chr14 + 100128744 100128744 100128744 TGCCATAGCTGGGGCCAAGCTGAGAAGAGTCCAACGGGTAAGAGCTCCTGTGTGCGGGGTGGGAA TGCCATAGCTGGGGCCAAGCTGAGAAGAGTCCGACGGGTAAGAGCTCCTGTGTGCGGGGTGGGAA A G EVL Ensembl:ENSG00000196405 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100128697..100128789 26863196 MeRIP-seq:(Medium) rs752083896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813997,Human_RBP_ID_1273596 Human_Splice_Rec_1552621,Human_Splice_Rec_1552647,Human_Splice_Rec_1552691,Human_Splice_Rec_1552733,Human_Splice_Rec_1552775,Human_Splice_Rec_1552787,Human_Splice_Rec_1552801 RMVar_hsa_circ_89358,RMVar_hsa_circ_6840,RMVar_hsa_circ_169017,RMVar_hsa_circ_100284,RMVar_hsa_circ_169019 60968 RMVar_ID_60968 Human_SNP_ID_567219540 m1A Human chr14 - 100137646 100137646 100137646 GCCTCGCTGCTCAGGCCTTCCTGGGGCAGCTCACCTGGACAGAATCGAGGACACAGGCTTCTCCA GCCTCGCTGCTCAGGCCTTCCTGGGGCAGCTCTCCTGGACAGAATCGAGGACACAGGCTTCTCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr14:100137638..100137710;chr14:100137524..100137819 26863196,32194978 MeRIP-seq:(Medium) rs111897088 Functional Loss SNV dbSNP153 33..33 33 - - - 60969 RMVar_ID_60969 Human_SNP_ID_567219995 m1A Human chr14 - 100139024 100139024 100139024 GGGCCCTGCGCATGAACACAATGCAAACTTCTAACTCCGCGCTCCCCCACACCCTCTTCCTCACC GGGCCCTGCGCATGAACACAATGCAAACTTCTTACTCCGCGCTCCCCCACACCCTCTTCCTCACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100138747..100139215 26863196 MeRIP-seq:(Medium) rs919002316 Functional Loss SNV dbSNP153 33..33 33 - - - 60970 RMVar_ID_60970 Human_SNP_ID_567219996 m1A Human chr14 + 100139025 100139025 100139025 GTGAGGAAGAGGGTGTGGGGGAGCGCGGAGTTAGAAGTTTGCATTGTGTTCATGCGCAGGGCCCA GTGAGGAAGAGGGTGTGGGGGAGCGCGGAGTTGGAAGTTTGCATTGTGTTCATGCGCAGGGCCCA A G EVL Ensembl:ENSG00000196405 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:100139015..100139116 26863196 MeRIP-seq:(Medium) rs938419514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880647,Human_RBP_ID_4280515,Human_RBP_ID_9418058 RMVar_hsa_circ_89358,RMVar_hsa_circ_6840,RMVar_hsa_circ_169017,RMVar_hsa_circ_100284,RMVar_hsa_circ_169019 60971 RMVar_ID_60971 Human_SNP_ID_567221319 m1A Human chr14 + 100143710 100143710 100143710 AGCCGCCGCCACCTGTCCCGCAGCCATCAGGCAGGAGCTGAGTGGGATCAGCACCACGTAAGGGG AGCCGCCGCCACCTGTCCCGCAGCCATCAGGCGGGAGCTGAGTGGGATCAGCACCACGTAAGGGG A G EVL Ensembl:ENSG00000196405 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100143699..100143831 26863196 MeRIP-seq:(Medium) rs774279850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882216,Human_RBP_ID_3944650,Human_RBP_ID_5112755,Human_RBP_ID_9369373,Human_RBP_ID_18979873,Human_RBP_ID_26325377,Human_RBP_ID_27809135 Human_Splice_Rec_1552636,Human_Splice_Rec_1552706,Human_Splice_Rec_1552748,Human_Splice_Rec_1552800,Human_Splice_Rec_1552832,Human_Splice_Rec_1552842,Human_Splice_Rec_1552848 RMVar_hsa_circ_89358,RMVar_hsa_circ_169017,RMVar_hsa_circ_100284,RMVar_hsa_circ_169019 60972 RMVar_ID_60972 Human_SNP_ID_567221415 m1A Human chr14 + 100143885 100143884 100143886 CTGCTGTGAAACGTCCTGACCTGTGATCACACATGACAGTGAGGAAACCAAGTGCAACTCCTGGG CTGCTGTGAAACGTCCTGACCTGTGATCACAC__GACAGTGAGGAAACCAAGTGCAACTCCTGGG CAT C EVL Ensembl:ENSG00000196405 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:100143736..100144186 32194978 MeRIP-seq:(Medium) rs1566737791 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1487440,Human_RBP_ID_1814114,Human_RBP_ID_4280532,Human_RBP_ID_12265518,Human_RBP_ID_18271514 Human_Splice_Rec_1552843 RMVar_hsa_circ_89358,RMVar_hsa_circ_169017,RMVar_hsa_circ_100284,RMVar_hsa_circ_169019 60973 RMVar_ID_60973 Human_SNP_ID_567227415 m1A Human chr14 + 100165169 100165169 100165169 GCCCACAGCCCACTACCTCCTCTGTCTCTCACACTCAGGGCCAATATTCCCCTGCCCTGATCACA GCCCACAGCCCACTACCTCCTCTGTCTCTCACTCTCAGGGCCAATATTCCCCTGCCCTGATCACA A T HSALNG0103703 RNACentral:URS0000E97A13 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100165161..100165226 26863196 MeRIP-seq:(Medium) rs1566745327 Functional Loss SNV dbSNP153 33..33 33 - - - 60974 RMVar_ID_60974 Human_SNP_ID_567228302 m1A Human chr14 + 100167203 100167203 100167203 TGGCTGCAGACAGGGCAGTCTCCCCCACACACACACCCGCTCCCACACACCCACCCGCTCCAACA TGGCTGCAGACAGGGCAGTCTCCCCCACACACCCACCCGCTCCCACACACCCACCCGCTCCAACA A C HSALNG0103703 RNACentral:URS0000E97A13 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100167192..100167257 26863196 MeRIP-seq:(Medium) rs1196680259 Functional Loss SNV dbSNP153 33..33 33 - - - 60975 RMVar_ID_60975 Human_SNP_ID_567247654 m1A Human chr14 + 100238194 100238194 100238194 GGCGAGATACCGGACGCTGCCCGCGTCGCCCGATTTTGTCCGTTCGGTCCTCCACACTCACCCCG GGCGAGATACCGGACGCTGCCCGCGTCGCCCGGTTTTGTCCGTTCGGTCCTCCACACTCACCCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100238145..100238261 26863196 MeRIP-seq:(Medium) rs1173972857 Functional Loss SNV dbSNP153 33..33 33 - - - 60976 RMVar_ID_60976 Human_SNP_ID_567248059 m1A Human chr14 - 100239133 100239133 100239133 TGGGGAAGGAAGGCAGAGGGAGGAAGGCGGCGAGCGGGCGGGGGGAGAGGGGGCGGGCGGCGGGG TGGGGAAGGAAGGCAGAGGGAGGAAGGCGGCGGGCGGGCGGGGGGAGAGGGGGCGGGCGGCGGGG T C lnc-DEGS2-3 RNACentral:URS00008C31D7 lincRNA intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr14:100239034..100239184 26863410 MeRIP-seq:(Medium) rs1327303655 Functional Loss SNV dbSNP153 33..33 33 - - - 60977 RMVar_ID_60977 Human_SNP_ID_567248219 m1A Human chr14 - 100239412 100239412 100239412 TGCCCGTGGCCGCCCCCGCCGCCGTGGTCGCCACCGCCGCCGTCCTCGTCGTCGTCGTCCTCCTC TGCCCGTGGCCGCCCCCGCCGCCGTGGTCGCCCCCGCCGCCGTCCTCGTCGTCGTCGTCCTCCTC T G lnc-DEGS2-3 RNACentral:URS00008C31D7 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:100239314..100239468 26863196 MeRIP-seq:(Medium) rs760870988 Functional Loss SNV dbSNP153 33..33 33 - - - 60978 RMVar_ID_60978 Human_SNP_ID_567248237 m1A Human chr14 + 100239438 100239438 100239438 CGGCGGTGGCGACCACGGCGGCGGGGGCGGCCACGGGCACGCCGGCCACCACCACCACCACCATC CGGCGGTGGCGACCACGGCGGCGGGGGCGGCCGCGGGCACGCCGGCCACCACCACCACCACCATC A G YY1 Ensembl:ENSG00000100811 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:100238785..100239700 26863410 MeRIP-seq:(Medium) rs376271434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4280606,Human_RBP_ID_27809136 Human_miRNA_ID_2027408 RMVar_hsa_circ_90088,RMVar_hsa_circ_169021 60979 RMVar_ID_60979 Human_SNP_ID_567248348 m1A Human chr14 - 100239648 100239648 100239648 TGTAGTCGTCGTCGCCGCCGGCCGGCGCGGGCACCGGGATGAGAATCTGATCCTCGAAGCCGTCC TGTAGTCGTCGTCGCCGCCGGCCGGCGCGGGCTCCGGGATGAGAATCTGATCCTCGAAGCCGTCC T A lnc-DEGS2-3 RNACentral:URS00008C31D7 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100239601..100239675 26863196 MeRIP-seq:(Medium) rs1306145498 Functional Loss SNV dbSNP153 33..33 33 - - - 60980 RMVar_ID_60980 Human_SNP_ID_567248401 m1A Human chr14 - 100239734 100239734 100239734 CTTCTTGACGCGGCCGCCTCCCGACGACGACGAGCCGCCGCCGCCGCTCTTGCCGGCCGCCGCCA CTTCTTGACGCGGCCGCCTCCCGACGACGACGGGCCGCCGCCGCCGCTCTTGCCGGCCGCCGCCA T C lnc-DEGS2-3 RNACentral:URS00008C31D7 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100239684..100239875 26863196 MeRIP-seq:(Medium) rs745977468 Functional Loss SNV dbSNP153 33..33 33 - - - 60981 RMVar_ID_60981 Human_SNP_ID_567248423 m1A Human chr14 + 100239782 100239770 100239782 GCGGCCGCGTCAAGAAGGGCGGCGGCAAGAAGAGCGGCAAGAAGAGTTACCTCAGCGGCGGGGCC GCGGCCGCGTCAAGAAGGGCG____________GCGGCAAGAAGAGTTACCTCAGCGGCGGGGCC GGCGGCAAGAAGA G YY1 Ensembl:ENSG00000100811 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100238713..100239926 26863196 MeRIP-seq:(Medium) rs776894477 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4309496,Human_RBP_ID_9369376 Human_miRNA_ID_1186,Human_miRNA_ID_4841,Human_miRNA_ID_8502,Human_miRNA_ID_15605,Human_miRNA_ID_19258,Human_miRNA_ID_22896,Human_miRNA_ID_26548,Human_miRNA_ID_1306012 RMVar_hsa_circ_90088,RMVar_hsa_circ_169021 60982 RMVar_ID_60982 Human_SNP_ID_567255310 m1A Human chr14 + 100262309 100262309 100262309 TAAAGATAATCTCATGATGTGTTTCAGATGAAAAAAAAGATATTGACCATGAGACAGTGGTTGAA TAAAGATAATCTCATGATGTGTTTCAGATGAAGAAAAAGATATTGACCATGAGACAGTGGTTGAA A G YY1 Ensembl:ENSG00000100811 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:100262301..100262350 26863196 MeRIP-seq:(Medium) rs1566776764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39381,Human_RBP_ID_441017,Human_RBP_ID_883474,Human_RBP_ID_1487466,Human_RBP_ID_1814132,Human_RBP_ID_2404316,Human_RBP_ID_5177348,Human_RBP_ID_17856967,Human_RBP_ID_22183083,Human_RBP_ID_26324725,Human_RBP_ID_26808607,Human_RBP_ID_26919788,Human_RBP_ID_27808534 Human_Splice_Rec_1552866,Human_Splice_Rec_1552874,Human_Splice_Rec_1552878,Human_Splice_Rec_1552884 RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_272218,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169022,RMVar_hsa_circ_169023 60983 RMVar_ID_60983 Human_SNP_ID_567260165 m1A Human chr14 - 100281446 100281446 100281446 CAGTGTATCCAGGACAAAGGGCCCGGAGCCAGACAGGTGCCCCCTACAGCCGAGGGTCCAAGGCA CAGTGTATCCAGGACAAAGGGCCCGGAGCCAGGCAGGTGCCCCCTACAGCCGAGGGTCCAAGGCA T C AL157871.6 Ensembl:ENSG00000259052 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:100281345..100281446 32194978 MeRIP-seq:(Medium) rs1026360031 Functional Loss SNV dbSNP153 33..33 33 - - - 60984 RMVar_ID_60984 Human_SNP_ID_567260418 m1A Human chr14 - 100282373 100282373 100282373 TCCGTGATGTGTGCGGACATTGTGCGGCCCCCAGAGAGAGCAGCAGACAGAACAGAGCACAGCAA TCCGTGATGTGTGCGGACATTGTGCGGCCCCCGGAGAGAGCAGCAGACAGAACAGAGCACAGCAA T C AL157871.6 Ensembl:ENSG00000259052 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:100282326..100282642 32194978 MeRIP-seq:(Medium) rs1054379828 Functional Loss SNV dbSNP153 33..33 33 - - - 60985 RMVar_ID_60985 Human_SNP_ID_567263528 m1A Human chr14 - 100292743 100292743 100292743 GATCTACGGGCACGAGGGTCTGCGTGGCGTCAACCGGGGCATGGTGTCCACGTTGCTGCGTGAGA GATCTACGGGCACGAGGGTCTGCGTGGCGTCAGCCGGGGCATGGTGTCCACGTTGCTGCGTGAGA T C SLC25A29 Ensembl:ENSG00000197119 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:100292252..100293508 32194978 MeRIP-seq:(Medium) rs1330326163 Functional Loss SNV dbSNP153 33..33 33 - - - 60986 RMVar_ID_60986 Human_SNP_ID_567267358 m1A Human chr14 + 100306408 100306408 100306408 GGTCAGGGATGGTGGGGATGGCGGCAGCAGCTAGACCCGCGCTGGTCCCTCGGCGGCAGCTGACT GGTCAGGGATGGTGGGGATGGCGGCAGCAGCTGGACCCGCGCTGGTCCCTCGGCGGCAGCTGACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:100306139..100306500 26863196 MeRIP-seq:(Medium) rs1373997840 Functional Loss SNV dbSNP153 33..33 33 - - - 60987 RMVar_ID_60987 Human_SNP_ID_567282646 m1A Human chr14 - 100361851 100361851 100361851 AAAAATGAGCTACAAAGCTGCCGCGGGGGAGGATTACAAGGCTGACTGTCCTCCAGGGAACCCAG AAAAATGAGCTACAAAGCTGCCGCGGGGGAGGTTTACAAGGCTGACTGTCCTCCAGGGAACCCAG T A WARS1 Ensembl:ENSG00000140105 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100361802..100361870 26863196 MeRIP-seq:(Medium) rs752171693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757215,Human_RBP_ID_882610,Human_RBP_ID_4280973,Human_RBP_ID_5087615,Human_RBP_ID_9256179,Human_RBP_ID_9282279,Human_RBP_ID_9324102,Human_RBP_ID_9369378,Human_RBP_ID_17363420,Human_RBP_ID_17844509,Human_RBP_ID_18435490,Human_RBP_ID_22439694,Human_RBP_ID_22758061,Human_RBP_ID_23610870,Human_RBP_ID_26325383 Human_Splice_Rec_1553006,Human_Splice_Rec_1553024,Human_Splice_Rec_1553044,Human_Splice_Rec_1553062,Human_Splice_Rec_1553084,Human_Splice_Rec_1553104,Human_Splice_Rec_1553138,Human_Splice_Rec_1553150,Human_Splice_Rec_1553172,Human_Splice_Rec_1553184,Human_Splice_Rec_1553192,Human_Splice_Rec_1553202,Human_Splice_Rec_1553210,Human_Splice_Rec_1553216,Human_Splice_Rec_1553222,Human_Splice_Rec_1553232,Human_Splice_Rec_1553240,Human_Splice_Rec_1553248,Human_Splice_Rec_1553258,Human_Splice_Rec_1553266,Human_Splice_Rec_1553274,Human_Splice_Rec_1553280,Human_Splice_Rec_1553288,Human_Splice_Rec_1553296,Human_Splice_Rec_1553302,Human_Splice_Rec_1553308,Human_Splice_Rec_1553314,Human_Splice_Rec_1553320,Human_Splice_Rec_1553326,Human_Splice_Rec_1553334,Human_Splice_Rec_1553342,Human_Splice_Rec_1553350,Human_Splice_Rec_1553356,Human_Splice_Rec_1553362,Human_Splice_Rec_1553368,Human_Splice_Rec_1553374 RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_108099,RMVar_hsa_circ_82436,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_95133,RMVar_hsa_circ_22120,RMVar_hsa_circ_315426,RMVar_hsa_circ_310387,RMVar_hsa_circ_169036,RMVar_hsa_circ_2855,RMVar_hsa_circ_266798,RMVar_hsa_circ_106497,RMVar_hsa_circ_169040,RMVar_hsa_circ_270155,RMVar_hsa_circ_288368,RMVar_hsa_circ_169041,RMVar_hsa_circ_121644,RMVar_hsa_circ_116703,RMVar_hsa_circ_169045,RMVar_hsa_circ_169046,RMVar_hsa_circ_169044,RMVar_hsa_circ_325870,RMVar_hsa_circ_169047,RMVar_hsa_circ_169048 60988 RMVar_ID_60988 Human_SNP_ID_567283188 m1A Human chr14 + 100364251 100364251 100364251 TCTGCTCTCTTTCTTAATACCTAAGACCTAGCATTGCTTCTTTAGTCCTGCTCAAACTATTTCCC TCTGCTCTCTTTCTTAATACCTAAGACCTAGCGTTGCTTCTTTAGTCCTGCTCAAACTATTTCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100364247..100364350 26863196 MeRIP-seq:(Medium) rs921793673 Functional Loss SNV dbSNP153 33..33 33 - - - 60989 RMVar_ID_60989 Human_SNP_ID_567284506 m1A Human chr14 - 100369134 100369134 100369134 CATCTCTGCTGGAGCTGTTCAACAGCATCGCCACACAAGGGGAGCTCGTAAGGTCCCTCAAAGCG CATCTCTGCTGGAGCTGTTCAACAGCATCGCCGCACAAGGGGAGCTCGTAAGGTCCCTCAAAGCG T C WARS1 Ensembl:ENSG00000140105 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:100369050..100369223 26863196 MeRIP-seq:(Medium) rs893565348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_997475,Human_RBP_ID_1487673,Human_RBP_ID_4280985,Human_RBP_ID_8798191,Human_RBP_ID_9282280,Human_RBP_ID_17246364,Human_RBP_ID_17844513,Human_RBP_ID_22438567,Human_RBP_ID_22758063,Human_RBP_ID_27642880 Human_Splice_Rec_1553005,Human_Splice_Rec_1553043,Human_Splice_Rec_1553083,Human_Splice_Rec_1553171,Human_Splice_Rec_1553183,Human_Splice_Rec_1553201,Human_Splice_Rec_1553209,Human_Splice_Rec_1553231,Human_Splice_Rec_1553239,Human_Splice_Rec_1553247,Human_Splice_Rec_1553255,Human_Splice_Rec_1553265,Human_Splice_Rec_1553273,Human_Splice_Rec_1553279,Human_Splice_Rec_1553285,Human_Splice_Rec_1553295,Human_Splice_Rec_1553301,Human_Splice_Rec_1553307,Human_Splice_Rec_1553313,Human_Splice_Rec_1553319,Human_Splice_Rec_1553323,Human_Splice_Rec_1553331,Human_Splice_Rec_1553341,Human_Splice_Rec_1553349,Human_Splice_Rec_1553355,Human_Splice_Rec_1553361,Human_Splice_Rec_1553367,Human_Splice_Rec_1553373,Human_Splice_Rec_1553375 Human_miRNA_ID_2076273,Human_miRNA_ID_2076274 RMVar_hsa_circ_92847,RMVar_hsa_circ_82436,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_95133,RMVar_hsa_circ_22120,RMVar_hsa_circ_315426,RMVar_hsa_circ_288368,RMVar_hsa_circ_169041,RMVar_hsa_circ_121644,RMVar_hsa_circ_116703,RMVar_hsa_circ_169045,RMVar_hsa_circ_169046,RMVar_hsa_circ_169047,RMVar_hsa_circ_298662,RMVar_hsa_circ_347813,RMVar_hsa_circ_377740 60990 RMVar_ID_60990 Human_SNP_ID_567286216 m1A Human chr14 - 100376207 100376207 100376207 CGGGGCGGAGTGAGGAAACAAGGGAGGGAGTGATGGAGGGACGCTGGCGCGGCGCCCAGTGGCCT CGGGGCGGAGTGAGGAAACAAGGGAGGGAGTGGTGGAGGGACGCTGGCGCGGCGCCCAGTGGCCT T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100376202..100376276 26863196 MeRIP-seq:(Medium) rs527525096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231223,Human_RBP_ID_5353327 RMVar_hsa_circ_95133,RMVar_hsa_circ_169047 60991 RMVar_ID_60991 Human_SNP_ID_567287911 m1A Human chr14 + 100382039 100382039 100382039 GAGGTGAGAGTGATTAGTGGGAGAAGAAAAGCAGGCCCAGGACCAAGCCCTGGGGACTGGGGACA GAGGTGAGAGTGATTAGTGGGAGAAGAAAAGCTGGCCCAGGACCAAGCCCTGGGGACTGGGGACA A T WDR25 Ensembl:ENSG00000176473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100382029..100382102 26863196 MeRIP-seq:(Medium) rs1009551872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6323280 RMVar_hsa_circ_319014,RMVar_hsa_circ_318768,RMVar_hsa_circ_169050 60992 RMVar_ID_60992 Human_SNP_ID_567288022 m1A Human chr14 - 100382398 100382398 100382398 AGCCAGCTCCCAGGCCCTCATGCTTGGAGCCAACACATACACAGGGCTCCTGCAGCCAAGCACGC AGCCAGCTCCCAGGCCCTCATGCTTGGAGCCATCACATACACAGGGCTCCTGCAGCCAAGCACGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100382390..100382455 26863196 MeRIP-seq:(Medium) rs1245311043 Functional Loss SNV dbSNP153 33..33 33 - - - 60993 RMVar_ID_60993 Human_SNP_ID_567288467 m1A Human chr14 + 100384433 100384433 100384433 AGGATGGGAAGACAGATTGGGAACCGGCGGGGAGCCAGGCAGGAGCTGTGGCCAGAAGTCCCGGC AGGATGGGAAGACAGATTGGGAACCGGCGGGGGGCCAGGCAGGAGCTGTGGCCAGAAGTCCCGGC A G WDR25 Ensembl:ENSG00000176473 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100384427..100384704 26863196 MeRIP-seq:(Medium) rs894716044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319014,RMVar_hsa_circ_318768,RMVar_hsa_circ_169050 60994 RMVar_ID_60994 Human_SNP_ID_567290695 m1A Human chr14 - 100394646 100394646 100394646 TATATTCCTGTTCCCAGCACAGATAGCCCTGGAGGGCCTTTCTCATCATCCCTCTCAAGTCTGCT TATATTCCTGTTCCCAGCACAGATAGCCCTGGGGGGCCTTTCTCATCATCCCTCTCAAGTCTGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100394641..100394741 26863196 MeRIP-seq:(Medium) rs1231365314 Functional Loss SNV dbSNP153 33..33 33 - - - 60995 RMVar_ID_60995 Human_SNP_ID_567293372 m1A Human chr14 + 100407017 100407017 100407017 GGAGCAGGAGCGAGGCTGCAGGTGTGAGAAGGACCCCGCCGTGCCAGGGCAGCCTCAAGGAGCTG GGAGCAGGAGCGAGGCTGCAGGTGTGAGAAGGCCCCCGCCGTGCCAGGGCAGCCTCAAGGAGCTG A C WDR25,AL135838.1 Ensembl:ENSG00000176473,Ensembl:ENSG00000258620 Protein coding,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:100406960..100407162;chr14:100406988..100407130 26863196 MeRIP-seq:(Medium) rs971887694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5565538 Human_Splice_Rec_1553484 RMVar_hsa_circ_319014,RMVar_hsa_circ_318768,RMVar_hsa_circ_169050 60996 RMVar_ID_60996 Human_SNP_ID_567299766 m1A Human chr14 - 100435015 100435015 100435015 GCACCTAGACGCACACTGCACAGTTCTCATGCACCTACATAACAGCCAAAATGGAGACCACAACA GCACCTAGACGCACACTGCACAGTTCTCATGCGCCTACATAACAGCCAAAATGGAGACCACAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100435009..100435078 26863196 MeRIP-seq:(Medium) rs1187563188 Functional Loss SNV dbSNP153 33..33 33 - - - 60997 RMVar_ID_60997 Human_SNP_ID_567303458 m1A Human chr14 - 100452498 100452498 100452498 GCTGCTGGGTTCCCTCAAGTCTCTACTCAGAGAGATGTTCCCTGAACCACACGATCTAAACACTG GCTGCTGGGTTCCCTCAAGTCTCTACTCAGAGGGATGTTCCCTGAACCACACGATCTAAACACTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100452492..100452612 26863196 MeRIP-seq:(Medium) rs767508298 Functional Loss SNV dbSNP153 33..33 33 - - - 60998 RMVar_ID_60998 Human_SNP_ID_567308451 m1A Human chr14 - 100474086 100474086 100474086 GGCGGCTGCTAACTGGACAAGGAGGCACATAAAGGGCGGCAGCCAGGGAACCCTCATCAGCTCAG GGCGGCTGCTAACTGGACAAGGAGGCACATAACGGGCGGCAGCCAGGGAACCCTCATCAGCTCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100474047..100474223 26863196 MeRIP-seq:(Medium) rs1435688209 Functional Loss SNV dbSNP153 33..33 33 - - - 60999 RMVar_ID_60999 Human_SNP_ID_567308454 m1A Human chr14 + 100474109 100474109 100474109 CTGCCGCCCTTTATGTGCCTCCTTGTCCAGTTAGCAGCCGCCTACTTTCTTGCCCACTTGTGAGT CTGCCGCCCTTTATGTGCCTCCTTGTCCAGTTGGCAGCCGCCTACTTTCTTGCCCACTTGTGAGT A G WDR25 Ensembl:ENSG00000176473 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:100474078..100474228 26863196 MeRIP-seq:(Medium) rs1004212416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318768,RMVar_hsa_circ_43004,RMVar_hsa_circ_281256,RMVar_hsa_circ_169051 61000 RMVar_ID_61000 Human_SNP_ID_567322939 m1A Human chr14 + 100537847 100537847 100537847 AGGGCTGGGGAGGAGAGGAGGTGCGGGGAGGAACAGACTCCTCGTTGTTGGCCGGGGCAGGGGAA AGGGCTGGGGAGGAGAGGAGGTGCGGGGAGGAGCAGACTCCTCGTTGTTGGCCGGGGCAGGGGAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100537761..100537900 26863196 MeRIP-seq:(Medium) rs1451581070 Functional Loss SNV dbSNP153 33..33 33 - - - 61001 RMVar_ID_61001 Human_SNP_ID_567323393 m1A Human chr14 - 100538741 100538741 100538741 CCTGAACAGCCGCGACGAGCTCTTCGACCGCAAGCCACCCGCCACCACCTACGAGGGCAGCCCTC CCTGAACAGCCGCGACGAGCTCTTCGACCGCAGGCCACCCGCCACCACCTACGAGGGCAGCCCTC T C BEGAIN Ensembl:ENSG00000183092 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:100538642..100538742 26863196 MeRIP-seq:(Medium) rs1222019538 Functional Loss SNV dbSNP153 33..33 33 - - - 61002 RMVar_ID_61002 Human_SNP_ID_567326519 m1A Human chr14 + 100549340 100549340 100549340 TCCATACCCTCACCACGTCCAGCCACCCACCTATGGCCCTCAGGCATCTCCACACCCAACCCGTC TCCATACCCTCACCACGTCCAGCCACCCACCTGTGGCCCTCAGGCATCTCCACACCCAACCCGTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100549229..100549492 26863196 MeRIP-seq:(Medium) rs1357552264 Functional Loss SNV dbSNP153 33..33 33 - - - 61003 RMVar_ID_61003 Human_SNP_ID_567326522 m1A Human chr14 + 100549349 100549349 100549349 TCACCACGTCCAGCCACCCACCTATGGCCCTCAGGCATCTCCACACCCAACCCGTCCAATGCAGC TCACCACGTCCAGCCACCCACCTATGGCCCTCGGGCATCTCCACACCCAACCCGTCCAATGCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:100548815..100549605;chr14:100548878..100549588 26863196 MeRIP-seq:(Medium) rs1006536458 Functional Loss SNV dbSNP153 33..33 33 - - - 61004 RMVar_ID_61004 Human_SNP_ID_567326768 m1A Human chr14 - 100550253 100550253 100550253 GCACAGCCTCACAGCCCTCAGCCCAGCATCCCAGCCAAGGGCTCCTTCCTTGGGCTTGGACCCCC GCACAGCCTCACAGCCCTCAGCCCAGCATCCCTGCCAAGGGCTCCTTCCTTGGGCTTGGACCCCC T A BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100550249..100550400 26863196 MeRIP-seq:(Medium) rs1002450070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2404726 61005 RMVar_ID_61005 Human_SNP_ID_567327901 m1A Human chr14 + 100554848 100554848 100554848 CAGTTCCTCACCCCAAATTCCTGTCCCCAGGGACCCGCCACAGCCCCAGCCTCGCCATTCCTGGC CAGTTCCTCACCCCAAATTCCTGTCCCCAGGGCCCCGCCACAGCCCCAGCCTCGCCATTCCTGGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr14:100554826..100554850;chr14:100554801..100555050;chr14:100554801..100554975 26863196 MeRIP-seq:(Medium) rs1022943999 Functional Loss SNV dbSNP153 33..33 33 - - - 61006 RMVar_ID_61006 Human_SNP_ID_567327974 m1A Human chr14 - 100555076 100555076 100555076 GGGGCCAACTGTAGGTTCTGCTGGGAAAGACCAGGCGAGGTCCGAGCAGCTTTGGGGACAAAGAC GGGGCCAACTGTAGGTTCTGCTGGGAAAGACCGGGCGAGGTCCGAGCAGCTTTGGGGACAAAGAC T C BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:100555051..100555075 26863196 MeRIP-seq:(Medium) rs944954209 Functional Loss SNV dbSNP153 33..33 33 - - - 61007 RMVar_ID_61007 Human_SNP_ID_567328048 m1A Human chr14 - 100555339 100555339 100555339 GAGCCATGAGGAACGAGGGTGGCCACGGGCACAGGGAACACAGGCCACCGGCACAGGAGAGGCTC GAGCCATGAGGAACGAGGGTGGCCACGGGCACGGGGAACACAGGCCACCGGCACAGGAGAGGCTC T C BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100555328..100555487 26863196 MeRIP-seq:(Medium) rs1287275188 Functional Loss SNV dbSNP153 33..33 33 - - - 61008 RMVar_ID_61008 Human_SNP_ID_567328279 m1A Human chr14 - 100556114 100556114 100556114 GAGCCCAAATCCACACCGTCAGGGTGGCCCCAATTGAGCTGGTGATGACCAAAGCTCACTCCTCT GAGCCCAAATCCACACCGTCAGGGTGGCCCCAGTTGAGCTGGTGATGACCAAAGCTCACTCCTCT T C BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100556107..100556318 26863196 MeRIP-seq:(Medium) rs575684892 Functional Loss SNV dbSNP153 33..33 33 - - - 61009 RMVar_ID_61009 Human_SNP_ID_567329006 m1A Human chr14 - 100558851 100558851 100558851 CCCCAAGGATGGGTCTGACGTTGGTTTCAAGGAGGTCTCGGGCTGAGAGCAGATGAGAGTAGCTG CCCCAAGGATGGGTCTGACGTTGGTTTCAAGGTGGTCTCGGGCTGAGAGCAGATGAGAGTAGCTG T A BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100558801..100558850 26863196 MeRIP-seq:(Medium) rs955425653 Functional Loss SNV dbSNP153 33..33 33 - - - 61010 RMVar_ID_61010 Human_SNP_ID_567329007 m1A Human chr14 - 100558851 100558851 100558851 CCCCAAGGATGGGTCTGACGTTGGTTTCAAGGAGGTCTCGGGCTGAGAGCAGATGAGAGTAGCTG CCCCAAGGATGGGTCTGACGTTGGTTTCAAGGCGGTCTCGGGCTGAGAGCAGATGAGAGTAGCTG T G BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:100558801..100558850 26863196 MeRIP-seq:(Medium) rs955425653 Functional Loss SNV dbSNP153 33..33 33 - - - 61011 RMVar_ID_61011 Human_SNP_ID_567329009 m1A Human chr14 + 100558859 100558859 100558859 CTCATCTGCTCTCAGCCCGAGACCTCCTTGAAACCAACGTCAGACCCATCCTTGGGGAGGTGGGC CTCATCTGCTCTCAGCCCGAGACCTCCTTGAAGCCAACGTCAGACCCATCCTTGGGGAGGTGGGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:100558851..100558875 26863196 MeRIP-seq:(Medium) rs985852670 Functional Loss SNV dbSNP153 33..33 33 - - - 61012 RMVar_ID_61012 Human_SNP_ID_567329058 m1A Human chr14 + 100559040 100559040 100559040 GGCCTGGGGTCAGCTGGCAGAAGGCCCTGAGCATGTGCTGAAGTATCTGATCCTCTTCCTGGGGG GGCCTGGGGTCAGCTGGCAGAAGGCCCTGAGCGTGTGCTGAAGTATCTGATCCTCTTCCTGGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100559033..100559168 26863196 MeRIP-seq:(Medium) rs1481380733 Functional Loss SNV dbSNP153 33..33 33 - - - 61013 RMVar_ID_61013 Human_SNP_ID_567329222 m1A Human chr14 + 100559789 100559789 100559789 GGATGCTCTTGGTCCCTGGCTGGTCCCACTCCACGTTCACCTCTGCATAGATGCGCACACAGACA GGATGCTCTTGGTCCCTGGCTGGTCCCACTCCGCGTTCACCTCTGCATAGATGCGCACACAGACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100559785..100560087 26863196 MeRIP-seq:(Medium) rs1159345047 Functional Loss SNV dbSNP153 33..33 33 - - - 61014 RMVar_ID_61014 Human_SNP_ID_567329581 m1A Human chr14 - 100561043 100561042 100561043 CATGTCAGGCCCGCATGGGGCTCCCCCTCCCCACCCCCCAACTACCACAGGCAGAAAATCCTTCC CATGTCAGGCCCGCATGGGGCTCCCCCTCCCC_CCCCCCAACTACCACAGGCAGAAAATCCTTCC GT G BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100561033..100561226 26863196 MeRIP-seq:(Medium) rs1566973457 Functional Loss DEL dbSNP153 33..33 33 - - - 61015 RMVar_ID_61015 Human_SNP_ID_567329582 m1A Human chr14 - 100561043 100561043 100561043 CATGTCAGGCCCGCATGGGGCTCCCCCTCCCCACCCCCCAACTACCACAGGCAGAAAATCCTTCC CATGTCAGGCCCGCATGGGGCTCCCCCTCCCCCCCCCCCAACTACCACAGGCAGAAAATCCTTCC T G BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100561033..100561226 26863196 MeRIP-seq:(Medium) rs1444527307 Functional Loss SNV dbSNP153 33..33 33 - - - 61016 RMVar_ID_61016 Human_SNP_ID_567330105 m1A Human chr14 - 100562892 100562892 100562892 CAGAGGCTGCTGTCGGCGCTGAGGACGCCGCAATGACTGCACAGGCGAATCTTCTAGTCGGCGGG CAGAGGCTGCTGTCGGCGCTGAGGACGCCGCAGTGACTGCACAGGCGAATCTTCTAGTCGGCGGG T C BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100562887..100563201 26863196 MeRIP-seq:(Medium) rs1026408522 Functional Loss SNV dbSNP153 33..33 33 - - - 61017 RMVar_ID_61017 Human_SNP_ID_567330433 m1A Human chr14 - 100564133 100564133 100564133 CCCGAGATCCCCCGAGACCCTTCCCCACAGACAGCCCCATCCTGCTCCCGGCCAGCCCCTAAGAT CCCGAGATCCCCCGAGACCCTTCCCCACAGACTGCCCCATCCTGCTCCCGGCCAGCCCCTAAGAT T A BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr14:100564041..100564189;chr14:100564001..100564165 26863196 MeRIP-seq:(Medium) rs948829799 Functional Loss SNV dbSNP153 33..33 33 - - - 61018 RMVar_ID_61018 Human_SNP_ID_567330524 m1A Human chr14 + 100564435 100564435 100564435 AGCTCAAATAGAAAAAGGGGCTGCCCAGCAGCACGCTGCAGGAGGCAGGCAGGAGGGACCCTGTT AGCTCAAATAGAAAAAGGGGCTGCCCAGCAGCTCGCTGCAGGAGGCAGGCAGGAGGGACCCTGTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100564426..100564550 26863196 MeRIP-seq:(Medium) rs569523957 Functional Loss SNV dbSNP153 33..33 33 - - - 61019 RMVar_ID_61019 Human_SNP_ID_567330694 m1A Human chr14 + 100565210 100565209 100565210 TCCACTTGGGAGGGAGGGGCAAGAGCGTCATGAAAACCCCAGGGAAAAGGCGACAGGGAAGACAC TCCACTTGGGAGGGAGGGGCAAGAGCGTCATG_AAACCCCAGGGAAAAGGCGACAGGGAAGACAC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100565171..100565425 26863196 MeRIP-seq:(Medium) rs1018920366 Functional Loss DEL dbSNP153 33..33 33 - - - 61020 RMVar_ID_61020 Human_SNP_ID_567331854 m1A Human chr14 + 100569512 100569510 100569512 GCGCTCAATAAACACGGACAGTGCATGCCTGGATCCTACGGCACTGGAGCCTGTCTTTCCTGGCC GCGCTCAATAAACACGGACAGTGCATGCCTG__TCCTACGGCACTGGAGCCTGTCTTTCCTGGCC GGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100569334..100569550 26863196 MeRIP-seq:(Medium) rs1390799907 Functional Loss DEL dbSNP153 32..33 33 - - - 61021 RMVar_ID_61021 Human_SNP_ID_567334683 m1A Human chr14 + 100580369 100580369 100580369 AAATCACAGGCCAGGTGACTAGACAACGTCACACCTTCATATACACTGCAAGGCCCTGACAATTG AAATCACAGGCCAGGTGACTAGACAACGTCACGCCTTCATATACACTGCAAGGCCCTGACAATTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100580366..100580642 26863196 MeRIP-seq:(Medium) rs538700176 Functional Loss SNV dbSNP153 33..33 33 - - - 61022 RMVar_ID_61022 Human_SNP_ID_567335404 m1A Human chr14 + 100583299 100583299 100583299 TCAATATACACTCATCACCTATCCATGCACTCACTCTTCCAGTGTCCATTCATTCCTCTGTCCAT TCAATATACACTCATCACCTATCCATGCACTCCCTCTTCCAGTGTCCATTCATTCCTCTGTCCAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100583294..100583666 26863196 MeRIP-seq:(Medium) rs1375403838 Functional Loss SNV dbSNP153 33..33 33 - - - 61023 RMVar_ID_61023 Human_SNP_ID_567336025 m1A Human chr14 - 100585463 100585463 100585463 GGCACTCCTGATGCTGAAGAGTGGATGGATGGATGAATGGATGGATGGATGGATGGATGGATGGA GGCACTCCTGATGCTGAAGAGTGGATGGATGGTTGAATGGATGGATGGATGGATGGATGGATGGA T A BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100585461..100585628 26863196 MeRIP-seq:(Medium) rs908617117 Functional Loss SNV dbSNP153 33..33 33 - - - 61024 RMVar_ID_61024 Human_SNP_ID_567336026 m1A Human chr14 - 100585463 100585463 100585463 GGCACTCCTGATGCTGAAGAGTGGATGGATGGATGAATGGATGGATGGATGGATGGATGGATGGA GGCACTCCTGATGCTGAAGAGTGGATGGATGGGTGAATGGATGGATGGATGGATGGATGGATGGA T C BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100585461..100585628 26863196 MeRIP-seq:(Medium) rs908617117 Functional Loss SNV dbSNP153 33..33 33 - - - 61025 RMVar_ID_61025 Human_SNP_ID_567364567 m1A Human chr14 + 100693044 100693044 100693044 TGCCTCCCTGAGCTCATTTCCTACCACTCGCCACCTCTCACTCCACCACAGCCACACGCACTTCC TGCCTCCCTGAGCTCATTTCCTACCACTCGCCGCCTCTCACTCCACCACAGCCACACGCACTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100692940..100693154 26863196 MeRIP-seq:(Medium) rs912146951 Functional Loss SNV dbSNP153 33..33 33 - - - 61026 RMVar_ID_61026 Human_SNP_ID_567370555 m1A Human chr14 - 100714665 100714665 100714665 GTGCCACCTCCTCCTGGAGGGCTTCCCTGAACACCCCTGCCAGGCAGAGCCGTCCACCACGATCC GTGCCACCTCCTCCTGGAGGGCTTCCCTGAACTCCCCTGCCAGGCAGAGCCGTCCACCACGATCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100714633..100714725 26863196 MeRIP-seq:(Medium) rs369102463 Functional Loss SNV dbSNP153 33..33 33 - - - 61027 RMVar_ID_61027 Human_SNP_ID_567370556 m1A Human chr14 - 100714665 100714665 100714665 GTGCCACCTCCTCCTGGAGGGCTTCCCTGAACACCCCTGCCAGGCAGAGCCGTCCACCACGATCC GTGCCACCTCCTCCTGGAGGGCTTCCCTGAACGCCCCTGCCAGGCAGAGCCGTCCACCACGATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100714633..100714725 26863196 MeRIP-seq:(Medium) rs369102463 Functional Loss SNV dbSNP153 33..33 33 - - - 61028 RMVar_ID_61028 Human_SNP_ID_567645803 m1A Human chr14 + 101761815 101761792 101761815 GCGGCGGCGGCGGCGGCGGCCGCGGGGGCGCGACGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCGGCGGCGG_______________________CGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCGGCGGCGGCCGCGGGGGCGCGA G PPP2R5C Ensembl:ENSG00000078304 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:101761772..101761923 26863196 MeRIP-seq:(Medium) rs1161774507 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_9323866,Human_RBP_ID_17363423,Human_RBP_ID_18435494 61029 RMVar_ID_61029 Human_SNP_ID_567645806 m1A Human chr14 + 101761815 101761798 101761815 GCGGCGGCGGCGGCGGCGGCCGCGGGGGCGCGACGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCGGCGGCGGCGGCGG_________________CGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCGGCCGCGGGGGCGCGA G PPP2R5C Ensembl:ENSG00000078304 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:101761772..101761923 26863196 MeRIP-seq:(Medium) rs1439250709 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_9323866,Human_RBP_ID_17363423,Human_RBP_ID_18435494 61030 RMVar_ID_61030 Human_SNP_ID_567645808 m1A Human chr14 + 101761815 101761801 101761815 GCGGCGGCGGCGGCGGCGGCCGCGGGGGCGCGACGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCGGCGGCGGCGGCGGCGG______________CGGCCGGGGCGGGGGCGCTGCTGCTGCGGGGG GCCGCGGGGGCGCGA G PPP2R5C Ensembl:ENSG00000078304 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:101761772..101761923 26863196 MeRIP-seq:(Medium) rs1241947288 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_9323866,Human_RBP_ID_17363423,Human_RBP_ID_18435494 61031 RMVar_ID_61031 Human_SNP_ID_567692950 m1A Human chr14 + 101948879 101948879 101948879 CAGTGAGGGTCAGAAGTGTCCGCGAGCCCTGTAGGCGAGGAGAGGCCTGGCTGAGGGCGCACAGC CAGTGAGGGTCAGAAGTGTCCGCGAGCCCTGTGGGCGAGGAGAGGCCTGGCTGAGGGCGCACAGC A G AL118558.3 Ensembl:ENSG00000271780 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:101948829..101948916 26863196 MeRIP-seq:(Medium) rs1362209646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5565217 61032 RMVar_ID_61032 Human_SNP_ID_567696998 m1A Human chr14 - 101964626 101964626 101964626 GAAGGCGGCCGCGACTCAGCGAGACAGCCAGCAAGAGACAGAAACGGCCGCCGGAAGCCGGACCG GAAGGCGGCCGCGACTCAGCGAGACAGCCAGCGAGAGACAGAAACGGCCGCCGGAAGCCGGACCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:101964576..101964750 26863196 MeRIP-seq:(Medium) rs1230598468 Functional Loss SNV dbSNP153 33..33 33 - - - 61033 RMVar_ID_61033 Human_SNP_ID_567697003 m1A Human chr14 - 101964645 101964645 101964645 GACCTTCCAGGAGCGATGAGAAGGCGGCCGCGACTCAGCGAGACAGCCAGCAAGAGACAGAAACG GACCTTCCAGGAGCGATGAGAAGGCGGCCGCGTCTCAGCGAGACAGCCAGCAAGAGACAGAAACG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:101964602..101964855 26863196 MeRIP-seq:(Medium) rs17511851 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - 61034 RMVar_ID_61034 Human_SNP_ID_567697024 m1A Human chr14 + 101964687 101964687 101964687 CTTCTCATCGCTCCTGGAAGGTCCCGAGCGCGACACCATGTCGGAGCCCGGGGGCGGCGGCGGCG CTTCTCATCGCTCCTGGAAGGTCCCGAGCGCGGCACCATGTCGGAGCCCGGGGGCGGCGGCGGCG A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:101964591..101964699 26863410 MeRIP-seq:(Medium) rs17511858 Functional Loss SNV dbSNP153,EGP,HGVD 33..33 33 - - - Human_RBP_ID_231346,Human_RBP_ID_4281183,Human_RBP_ID_8797985,Human_RBP_ID_9282287,Human_RBP_ID_9323872,Human_RBP_ID_17669232,Human_RBP_ID_18418297,Human_RBP_ID_22439447 Clinvar_Rec_217,Clinvar_Rec_218,Clinvar_Rec_219,Clinvar_Rec_220,Clinvar_Rec_221 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169153,RMVar_hsa_circ_94226,RMVar_hsa_circ_117712,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_169154 61035 RMVar_ID_61035 Human_SNP_ID_567702493 m1A Human chr14 - 101985827 101985827 101985827 GCTTCCGTGCCCTCTTTGGAAACATCCAGTCCATCCACTTCCTTGACGTTCTCATAAGCAAGGTT GCTTCCGTGCCCTCTTTGGAAACATCCAGTCCGTCCACTTCCTTGACGTTCTCATAAGCAAGGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:101985777..101985894 26863196 MeRIP-seq:(Medium) rs1407361267 Functional Loss SNV dbSNP153 33..33 33 - - - 61036 RMVar_ID_61036 Human_SNP_ID_567702611 m1A Human chr14 + 101986296 101986296 101986296 AGAAGCTGAAGCAGGATGGAGACAGCTTCCGCATGAAGCTCAACACGCAGGAGATCTTTGATGAC AGAAGCTGAAGCAGGATGGAGACAGCTTCCGCCTGAAGCTCAACACGCAGGAGATCTTTGATGAC A C DYNC1H1 Ensembl:ENSG00000197102 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:101986251..101986300 26863196 MeRIP-seq:(Medium) rs745510694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757476,Human_RBP_ID_4281275,Human_RBP_ID_5522893,Human_RBP_ID_17856499,Human_RBP_ID_22711286 Clinvar_Rec_222 RMVar_hsa_circ_68392,RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_117712,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_169154,RMVar_hsa_circ_105470,RMVar_hsa_circ_312055,RMVar_hsa_circ_342506,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_117557,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_122668,RMVar_hsa_circ_124549,RMVar_hsa_circ_119991,RMVar_hsa_circ_169161,RMVar_hsa_circ_169165,RMVar_hsa_circ_100522,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_169163,RMVar_hsa_circ_169164,RMVar_hsa_circ_169162,RMVar_hsa_circ_121278,RMVar_hsa_circ_90885,RMVar_hsa_circ_83551,RMVar_hsa_circ_115595,RMVar_hsa_circ_169168,RMVar_hsa_circ_169169,RMVar_hsa_circ_119288,RMVar_hsa_circ_77296,RMVar_hsa_circ_169173,RMVar_hsa_circ_169174,RMVar_hsa_circ_169172,RMVar_hsa_circ_302019,RMVar_hsa_circ_332616,RMVar_hsa_circ_106610,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_125875,RMVar_hsa_circ_169176,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169180,RMVar_hsa_circ_169178,RMVar_hsa_circ_324430,RMVar_hsa_circ_102363,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_85393,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169182,RMVar_hsa_circ_169183,RMVar_hsa_circ_169181 61037 RMVar_ID_61037 Human_SNP_ID_567707604 m1A Human chr14 + 102005139 102005123 102005140 CATGGGCGGAGGTGGAGATGCCGCGCCCTTGCACTCTGTGCTGAGCAATGTGGAGGTCACCCTCA CATGGGCGGAGGTGGAG_________________TCTGTGCTGAGCAATGTGGAGGTCACCCTCA GATGCCGCGCCCTTGCAC G DYNC1H1 Ensembl:ENSG00000197102 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102005026..102005150 32194978 MeRIP-seq:(Medium) rs1185382775 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_120629,Human_RBP_ID_1487835,Human_RBP_ID_1814457,Human_RBP_ID_8792522,Human_RBP_ID_9256225,Human_RBP_ID_9281369,Human_RBP_ID_22438937,Human_RBP_ID_24368230 Human_Splice_Rec_1555716,Human_Splice_Rec_1555717,Human_Splice_Rec_1555776,Human_Splice_Rec_1555777,Human_Splice_Rec_1555892,Human_Splice_Rec_1555893 Human_miRNA_ID_2019803,Human_miRNA_ID_2024898,Human_miRNA_ID_2311515,Human_miRNA_ID_2313533,Human_miRNA_ID_2499629,Human_miRNA_ID_2607410,Human_miRNA_ID_2655319 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_124549,RMVar_hsa_circ_119991,RMVar_hsa_circ_169165,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_90885,RMVar_hsa_circ_8271,RMVar_hsa_circ_83551,RMVar_hsa_circ_115595,RMVar_hsa_circ_169168,RMVar_hsa_circ_169169,RMVar_hsa_circ_119288,RMVar_hsa_circ_77296,RMVar_hsa_circ_169173,RMVar_hsa_circ_169174,RMVar_hsa_circ_169172,RMVar_hsa_circ_106610,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_125875,RMVar_hsa_circ_169176,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169180,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_85393,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169182,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169202,RMVar_hsa_circ_97875,RMVar_hsa_circ_169201,RMVar_hsa_circ_110171,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169205,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_77743,RMVar_hsa_circ_87202,RMVar_hsa_circ_109420,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169210,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_96241,RMVar_hsa_circ_114823,RMVar_hsa_circ_169214,RMVar_hsa_circ_81418,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_169215,RMVar_hsa_circ_169213,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_359178,RMVar_hsa_circ_117510,RMVar_hsa_circ_105884,RMVar_hsa_circ_70271,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169225,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_101542,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169234,RMVar_hsa_circ_169232,RMVar_hsa_circ_348666,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_27120,RMVar_hsa_circ_2934,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_328926,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_169250,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_323139,RMVar_hsa_circ_169246,RMVar_hsa_circ_14579,RMVar_hsa_circ_169251,RMVar_hsa_circ_105156,RMVar_hsa_circ_344963,RMVar_hsa_circ_82924,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_169254 61038 RMVar_ID_61038 Human_SNP_ID_567708949 m1A Human chr14 - 102010435 102010435 102010435 TAACGAACCTCTTGTTCAGGGAGATTTTCAGCAATTTCTCCTTCATCAACTGCTTCCCCTCGTTC TAACGAACCTCTTGTTCAGGGAGATTTTCAGCGATTTCTCCTTCATCAACTGCTTCCCCTCGTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102010384..102010467 26863196 MeRIP-seq:(Medium) rs759525537 Functional Loss SNV dbSNP153 33..33 33 - - - 61039 RMVar_ID_61039 Human_SNP_ID_567709100 m1A Human chr14 - 102010931 102010931 102010931 ATCCAAGTTACCTTTTCAACCCACATTCCACCAACTTCTTCTCCATCTCCATATGTCAAATACAT ATCCAAGTTACCTTTTCAACCCACATTCCACCGACTTCTTCTCCATCTCCATATGTCAAATACAT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:102010801..102011013 26863196 MeRIP-seq:(Medium) rs1305195955 Functional Loss SNV dbSNP153 33..33 33 - - - 61040 RMVar_ID_61040 Human_SNP_ID_567710124 m1A Human chr14 + 102015217 102015217 102015217 TGAGGATGTGCTGAGCACCGACATGATCTTCAACAACTTCCTGGCCAGGCTGCGCAGCATCCCGC TGAGGATGTGCTGAGCACCGACATGATCTTCAGCAACTTCCTGGCCAGGCTGCGCAGCATCCCGC A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102015167..102015279 26863196 MeRIP-seq:(Medium) rs775274723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40226,Human_RBP_ID_997493,Human_RBP_ID_1170933,Human_RBP_ID_1487850,Human_RBP_ID_1814483,Human_RBP_ID_4281520,Human_RBP_ID_8792570,Human_RBP_ID_9281377,Human_RBP_ID_17844656,Human_RBP_ID_18469457,Human_RBP_ID_18644984 Human_miRNA_ID_2567161,Human_miRNA_ID_2977510 RMVar_hsa_circ_2890,RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_119991,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_8271,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169201,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_114823,RMVar_hsa_circ_81418,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_169215,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_70271,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_169251,RMVar_hsa_circ_82924,RMVar_hsa_circ_113873,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_126755,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_169256,RMVar_hsa_circ_345503,RMVar_hsa_circ_58723,RMVar_hsa_circ_125284,RMVar_hsa_circ_39229,RMVar_hsa_circ_9183,RMVar_hsa_circ_124056,RMVar_hsa_circ_79196,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169259,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169264,RMVar_hsa_circ_169262,RMVar_hsa_circ_81152,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_111075,RMVar_hsa_circ_169270,RMVar_hsa_circ_44373,RMVar_hsa_circ_169271,RMVar_hsa_circ_45006,RMVar_hsa_circ_169272,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_7580,RMVar_hsa_circ_102087,RMVar_hsa_circ_372806,RMVar_hsa_circ_169275,RMVar_hsa_circ_327745,RMVar_hsa_circ_96665,RMVar_hsa_circ_169277,RMVar_hsa_circ_169278,RMVar_hsa_circ_169279 61041 RMVar_ID_61041 Human_SNP_ID_567710730 m1A Human chr14 + 102017501 102017501 102017501 CCCCACAGACCCTGGAAGAAAGCCCCTCTCACACAGGTAAAACAGCTCGGTAGACTGCTCTGCTT CCCCACAGACCCTGGAAGAAAGCCCCTCTCACCCAGGTAAAACAGCTCGGTAGACTGCTCTGCTT A C DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr14:102017476..102017525;chr14:102017401..102017606 26863196 MeRIP-seq:(Medium) rs1300180362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18189426,Human_RBP_ID_26808247 Human_Splice_Rec_1555805,Human_Splice_Rec_1555919,Human_Splice_Rec_1555999,Human_Splice_Rec_1556093,Human_Splice_Rec_1556103,Human_Splice_Rec_1556175 RMVar_hsa_circ_2890,RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_119991,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169201,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_114823,RMVar_hsa_circ_81418,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_169215,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_70271,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_169251,RMVar_hsa_circ_82924,RMVar_hsa_circ_113873,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_169256,RMVar_hsa_circ_345503,RMVar_hsa_circ_58723,RMVar_hsa_circ_125284,RMVar_hsa_circ_39229,RMVar_hsa_circ_124056,RMVar_hsa_circ_79196,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169264,RMVar_hsa_circ_169262,RMVar_hsa_circ_81152,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_111075,RMVar_hsa_circ_169270,RMVar_hsa_circ_169271,RMVar_hsa_circ_169272,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_102087,RMVar_hsa_circ_372806,RMVar_hsa_circ_169275,RMVar_hsa_circ_96665,RMVar_hsa_circ_100732,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169277,RMVar_hsa_circ_169278,RMVar_hsa_circ_169279,RMVar_hsa_circ_313534,RMVar_hsa_circ_333286,RMVar_hsa_circ_88918,RMVar_hsa_circ_108422,RMVar_hsa_circ_169280,RMVar_hsa_circ_169281,RMVar_hsa_circ_103111,RMVar_hsa_circ_169283,RMVar_hsa_circ_42988,RMVar_hsa_circ_169284,RMVar_hsa_circ_169282,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_110350,RMVar_hsa_circ_169285,RMVar_hsa_circ_169289,RMVar_hsa_circ_76682,RMVar_hsa_circ_93679,RMVar_hsa_circ_169290,RMVar_hsa_circ_169287,RMVar_hsa_circ_169288,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_117296,RMVar_hsa_circ_80861,RMVar_hsa_circ_117167,RMVar_hsa_circ_169292,RMVar_hsa_circ_169293,RMVar_hsa_circ_169294,RMVar_hsa_circ_127573,RMVar_hsa_circ_169295,RMVar_hsa_circ_169296 61042 RMVar_ID_61042 Human_SNP_ID_567711057 m1A Human chr14 - 102018599 102018599 102018599 AGAAACTCTGCGTACCTGAGACATGGTGTAGAACTCCACCATGGCAGCAGTGAGCGGCTCTGCAT AGAAACTCTGCGTACCTGAGACATGGTGTAGATCTCCACCATGGCAGCAGTGAGCGGCTCTGCAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:102018551..102018600 26863196 MeRIP-seq:(Medium) rs748320904 Functional Loss SNV dbSNP153 33..33 33 - - - 61043 RMVar_ID_61043 Human_SNP_ID_567711345 m1A Human chr14 + 102019805 102019805 102019805 TTAAATATTTCAGGGTCTAGGTTCTTTAATGTAAACATGTTTTGCCACATTTTACCTTTTGACCA TTAAATATTTCAGGGTCTAGGTTCTTTAATGTCAACATGTTTTGCCACATTTTACCTTTTGACCA A C DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:102019804..102020025 26863196 MeRIP-seq:(Medium) rs1260176354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_119991,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169201,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_114823,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_169251,RMVar_hsa_circ_82924,RMVar_hsa_circ_113873,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_169256,RMVar_hsa_circ_58723,RMVar_hsa_circ_125284,RMVar_hsa_circ_39229,RMVar_hsa_circ_124056,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169262,RMVar_hsa_circ_81152,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_111075,RMVar_hsa_circ_169270,RMVar_hsa_circ_169271,RMVar_hsa_circ_169272,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_102087,RMVar_hsa_circ_372806,RMVar_hsa_circ_169275,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169278,RMVar_hsa_circ_169279,RMVar_hsa_circ_333286,RMVar_hsa_circ_88918,RMVar_hsa_circ_108422,RMVar_hsa_circ_169280,RMVar_hsa_circ_169281,RMVar_hsa_circ_103111,RMVar_hsa_circ_169283,RMVar_hsa_circ_42988,RMVar_hsa_circ_169284,RMVar_hsa_circ_169282,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_110350,RMVar_hsa_circ_169285,RMVar_hsa_circ_169289,RMVar_hsa_circ_76682,RMVar_hsa_circ_93679,RMVar_hsa_circ_169287,RMVar_hsa_circ_169288,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_117296,RMVar_hsa_circ_80861,RMVar_hsa_circ_62402,RMVar_hsa_circ_117167,RMVar_hsa_circ_169292,RMVar_hsa_circ_169293,RMVar_hsa_circ_169294,RMVar_hsa_circ_127573,RMVar_hsa_circ_303827,RMVar_hsa_circ_169295,RMVar_hsa_circ_169296,RMVar_hsa_circ_312872,RMVar_hsa_circ_322984,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_169298,RMVar_hsa_circ_169300,RMVar_hsa_circ_169299,RMVar_hsa_circ_169297 61044 RMVar_ID_61044 Human_SNP_ID_567711371 m1A Human chr14 + 102019921 102019921 102019921 ATAGGAGAGATTCACCCAGGATACACAACCTCACTATATCTATTCACCCCGTGAAATGACTAGGT ATAGGAGAGATTCACCCAGGATACACAACCTCTCTATATCTATTCACCCCGTGAAATGACTAGGT A T DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:102019901..102019925 26863196 MeRIP-seq:(Medium) rs190094426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1814493,Human_RBP_ID_8792601,Human_RBP_ID_9281381,Human_RBP_ID_17246471,Human_RBP_ID_17361372,Human_RBP_ID_17478228,Human_RBP_ID_17686796,Human_RBP_ID_17844658,Human_RBP_ID_18528153,Human_RBP_ID_18644997,Human_RBP_ID_22421280,Human_RBP_ID_27642941 Human_Splice_Rec_1555808,Human_Splice_Rec_1555922,Human_Splice_Rec_1556002,Human_Splice_Rec_1556096,Human_Splice_Rec_1556106,Human_Splice_Rec_1556178 Human_miRNA_ID_2007332 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_119991,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169201,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_114823,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_169251,RMVar_hsa_circ_82924,RMVar_hsa_circ_113873,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_169256,RMVar_hsa_circ_58723,RMVar_hsa_circ_125284,RMVar_hsa_circ_39229,RMVar_hsa_circ_124056,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169262,RMVar_hsa_circ_81152,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_111075,RMVar_hsa_circ_169270,RMVar_hsa_circ_169271,RMVar_hsa_circ_169272,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_102087,RMVar_hsa_circ_372806,RMVar_hsa_circ_169275,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169278,RMVar_hsa_circ_169279,RMVar_hsa_circ_333286,RMVar_hsa_circ_88918,RMVar_hsa_circ_108422,RMVar_hsa_circ_169280,RMVar_hsa_circ_169281,RMVar_hsa_circ_103111,RMVar_hsa_circ_169283,RMVar_hsa_circ_42988,RMVar_hsa_circ_169284,RMVar_hsa_circ_169282,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_110350,RMVar_hsa_circ_169285,RMVar_hsa_circ_169289,RMVar_hsa_circ_76682,RMVar_hsa_circ_93679,RMVar_hsa_circ_169287,RMVar_hsa_circ_169288,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_117296,RMVar_hsa_circ_80861,RMVar_hsa_circ_62402,RMVar_hsa_circ_117167,RMVar_hsa_circ_169292,RMVar_hsa_circ_169293,RMVar_hsa_circ_169294,RMVar_hsa_circ_127573,RMVar_hsa_circ_303827,RMVar_hsa_circ_169295,RMVar_hsa_circ_169296,RMVar_hsa_circ_312872,RMVar_hsa_circ_322984,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169300,RMVar_hsa_circ_169299,RMVar_hsa_circ_169297,RMVar_hsa_circ_278395,RMVar_hsa_circ_169302,RMVar_hsa_circ_169303 61045 RMVar_ID_61045 Human_SNP_ID_567715993 m1A Human chr14 + 102038519 102038518 102038520 AACCCGGTGCTGAACCGTGAAGTGCGGCGAACAGGGGGGAGAGTGCTGATCACTCTCGGGGACCA AACCCGGTGCTGAACCGTGAAGTGCGGCGAAC__GGGGGAGAGTGCTGATCACTCTCGGGGACCA CAG C DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102038451..102038550 32194978 MeRIP-seq:(Medium) rs1567020949 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_757499,Human_RBP_ID_881107,Human_RBP_ID_3441530,Human_RBP_ID_4281704,Human_RBP_ID_5522931,Human_RBP_ID_8798283,Human_RBP_ID_9282381,Human_RBP_ID_18469460,Human_RBP_ID_18980978,Human_RBP_ID_22758395 Human_Splice_Rec_1555840,Human_Splice_Rec_1555841,Human_Splice_Rec_1556034,Human_Splice_Rec_1556035,Human_Splice_Rec_1556138,Human_Splice_Rec_1556139,Human_Splice_Rec_1556282,Human_Splice_Rec_1556283,Human_Splice_Rec_1556324,Human_Splice_Rec_1556325,Human_Splice_Rec_1556384,Human_Splice_Rec_1556385,Human_Splice_Rec_1556448,Human_Splice_Rec_1556449,Human_Splice_Rec_1556486,Human_Splice_Rec_1556487,Human_Splice_Rec_1556549 Human_miRNA_ID_1979292 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169158,RMVar_hsa_circ_103974,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_122969,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169208,RMVar_hsa_circ_97713,RMVar_hsa_circ_114823,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_124093,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_77475,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_82924,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_125284,RMVar_hsa_circ_124056,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169262,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_169270,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_102087,RMVar_hsa_circ_169275,RMVar_hsa_circ_96466,RMVar_hsa_circ_88408,RMVar_hsa_circ_169279,RMVar_hsa_circ_108422,RMVar_hsa_circ_169280,RMVar_hsa_circ_103111,RMVar_hsa_circ_169283,RMVar_hsa_circ_169284,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_169285,RMVar_hsa_circ_76682,RMVar_hsa_circ_169287,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_117296,RMVar_hsa_circ_80861,RMVar_hsa_circ_117167,RMVar_hsa_circ_169292,RMVar_hsa_circ_169293,RMVar_hsa_circ_169294,RMVar_hsa_circ_169296,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169297,RMVar_hsa_circ_169303,RMVar_hsa_circ_127230,RMVar_hsa_circ_99306,RMVar_hsa_circ_82087,RMVar_hsa_circ_169306,RMVar_hsa_circ_169307,RMVar_hsa_circ_169308,RMVar_hsa_circ_169305,RMVar_hsa_circ_81266,RMVar_hsa_circ_110513,RMVar_hsa_circ_30290,RMVar_hsa_circ_97484,RMVar_hsa_circ_169309,RMVar_hsa_circ_169310,RMVar_hsa_circ_116090,RMVar_hsa_circ_169314,RMVar_hsa_circ_101794,RMVar_hsa_circ_169316,RMVar_hsa_circ_78327,RMVar_hsa_circ_169317,RMVar_hsa_circ_169318,RMVar_hsa_circ_93345,RMVar_hsa_circ_115331,RMVar_hsa_circ_169322,RMVar_hsa_circ_98214,RMVar_hsa_circ_169321,RMVar_hsa_circ_39731,RMVar_hsa_circ_81008,RMVar_hsa_circ_169323,RMVar_hsa_circ_56386,RMVar_hsa_circ_88704,RMVar_hsa_circ_113056,RMVar_hsa_circ_169324,RMVar_hsa_circ_330906,RMVar_hsa_circ_169325,RMVar_hsa_circ_84093,RMVar_hsa_circ_169327,RMVar_hsa_circ_169326,RMVar_hsa_circ_108051,RMVar_hsa_circ_118168,RMVar_hsa_circ_169329,RMVar_hsa_circ_169330,RMVar_hsa_circ_169331,RMVar_hsa_circ_371950,RMVar_hsa_circ_100206,RMVar_hsa_circ_13373,RMVar_hsa_circ_102947,RMVar_hsa_circ_169332,RMVar_hsa_circ_169333,RMVar_hsa_circ_348045,RMVar_hsa_circ_375174,RMVar_hsa_circ_71435,RMVar_hsa_circ_77105,RMVar_hsa_circ_27209,RMVar_hsa_circ_169334,RMVar_hsa_circ_169335,RMVar_hsa_circ_169336 61046 RMVar_ID_61046 Human_SNP_ID_567715994 m1A Human chr14 + 102038519 102038519 102038519 AACCCGGTGCTGAACCGTGAAGTGCGGCGAACAGGGGGGAGAGTGCTGATCACTCTCGGGGACCA AACCCGGTGCTGAACCGTGAAGTGCGGCGAACGGGGGGGAGAGTGCTGATCACTCTCGGGGACCA A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102038451..102038550 32194978 MeRIP-seq:(Medium) rs773944980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757499,Human_RBP_ID_881107,Human_RBP_ID_3441530,Human_RBP_ID_4281704,Human_RBP_ID_5522931,Human_RBP_ID_8798283,Human_RBP_ID_9282381,Human_RBP_ID_18469460,Human_RBP_ID_18980978,Human_RBP_ID_22758395 Human_Splice_Rec_1555840,Human_Splice_Rec_1555841,Human_Splice_Rec_1556034,Human_Splice_Rec_1556035,Human_Splice_Rec_1556138,Human_Splice_Rec_1556139,Human_Splice_Rec_1556282,Human_Splice_Rec_1556283,Human_Splice_Rec_1556324,Human_Splice_Rec_1556325,Human_Splice_Rec_1556384,Human_Splice_Rec_1556385,Human_Splice_Rec_1556448,Human_Splice_Rec_1556449,Human_Splice_Rec_1556486,Human_Splice_Rec_1556487,Human_Splice_Rec_1556549 Human_miRNA_ID_1979292 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169158,RMVar_hsa_circ_103974,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169177,RMVar_hsa_circ_122969,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169208,RMVar_hsa_circ_97713,RMVar_hsa_circ_114823,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_124093,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_77475,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_169237,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_82924,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_125284,RMVar_hsa_circ_124056,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169262,RMVar_hsa_circ_115030,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_169270,RMVar_hsa_circ_109715,RMVar_hsa_circ_169276,RMVar_hsa_circ_116877,RMVar_hsa_circ_169273,RMVar_hsa_circ_118983,RMVar_hsa_circ_102087,RMVar_hsa_circ_169275,RMVar_hsa_circ_96466,RMVar_hsa_circ_88408,RMVar_hsa_circ_169279,RMVar_hsa_circ_108422,RMVar_hsa_circ_169280,RMVar_hsa_circ_103111,RMVar_hsa_circ_169283,RMVar_hsa_circ_169284,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_169285,RMVar_hsa_circ_76682,RMVar_hsa_circ_169287,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_117296,RMVar_hsa_circ_80861,RMVar_hsa_circ_117167,RMVar_hsa_circ_169292,RMVar_hsa_circ_169293,RMVar_hsa_circ_169294,RMVar_hsa_circ_169296,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169297,RMVar_hsa_circ_169303,RMVar_hsa_circ_127230,RMVar_hsa_circ_99306,RMVar_hsa_circ_82087,RMVar_hsa_circ_169306,RMVar_hsa_circ_169307,RMVar_hsa_circ_169308,RMVar_hsa_circ_169305,RMVar_hsa_circ_81266,RMVar_hsa_circ_110513,RMVar_hsa_circ_30290,RMVar_hsa_circ_97484,RMVar_hsa_circ_169309,RMVar_hsa_circ_169310,RMVar_hsa_circ_116090,RMVar_hsa_circ_169314,RMVar_hsa_circ_101794,RMVar_hsa_circ_169316,RMVar_hsa_circ_78327,RMVar_hsa_circ_169317,RMVar_hsa_circ_169318,RMVar_hsa_circ_93345,RMVar_hsa_circ_115331,RMVar_hsa_circ_169322,RMVar_hsa_circ_98214,RMVar_hsa_circ_169321,RMVar_hsa_circ_39731,RMVar_hsa_circ_81008,RMVar_hsa_circ_169323,RMVar_hsa_circ_56386,RMVar_hsa_circ_88704,RMVar_hsa_circ_113056,RMVar_hsa_circ_169324,RMVar_hsa_circ_330906,RMVar_hsa_circ_169325,RMVar_hsa_circ_84093,RMVar_hsa_circ_169327,RMVar_hsa_circ_169326,RMVar_hsa_circ_108051,RMVar_hsa_circ_118168,RMVar_hsa_circ_169329,RMVar_hsa_circ_169330,RMVar_hsa_circ_169331,RMVar_hsa_circ_371950,RMVar_hsa_circ_100206,RMVar_hsa_circ_13373,RMVar_hsa_circ_102947,RMVar_hsa_circ_169332,RMVar_hsa_circ_169333,RMVar_hsa_circ_348045,RMVar_hsa_circ_375174,RMVar_hsa_circ_71435,RMVar_hsa_circ_77105,RMVar_hsa_circ_27209,RMVar_hsa_circ_169334,RMVar_hsa_circ_169335,RMVar_hsa_circ_169336 61047 RMVar_ID_61047 Human_SNP_ID_567716904 m1A Human chr14 + 102041651 102041651 102041651 TCCGGCCCGATCGCCTGTTGGCCATGGCCCACATGTTTGTTTCAACAAACCTTGGGGAGTCTTTC TCCGGCCCGATCGCCTGTTGGCCATGGCCCACGTGTTTGTTTCAACAAACCTTGGGGAGTCTTTC A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102041601..102041650 32194978 MeRIP-seq:(Medium) rs765542840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1814552,Human_RBP_ID_4309865,Human_RBP_ID_18645055 Human_Splice_Rec_1555854,Human_Splice_Rec_1555855,Human_Splice_Rec_1556048,Human_Splice_Rec_1556049,Human_Splice_Rec_1556148,Human_Splice_Rec_1556149,Human_Splice_Rec_1556222,Human_Splice_Rec_1556223,Human_Splice_Rec_1556296,Human_Splice_Rec_1556297,Human_Splice_Rec_1556338,Human_Splice_Rec_1556339,Human_Splice_Rec_1556398,Human_Splice_Rec_1556399,Human_Splice_Rec_1556462,Human_Splice_Rec_1556463,Human_Splice_Rec_1556500,Human_Splice_Rec_1556501,Human_Splice_Rec_1556534,Human_Splice_Rec_1556535,Human_Splice_Rec_1556558,Human_Splice_Rec_1556559,Human_Splice_Rec_1556564,Human_Splice_Rec_1556565,Human_Splice_Rec_1556591 Human_miRNA_ID_2297614,Human_miRNA_ID_2734194,Human_miRNA_ID_2905343,Human_miRNA_ID_2977512 RMVar_hsa_circ_121811,RMVar_hsa_circ_169156,RMVar_hsa_circ_112765,RMVar_hsa_circ_169157,RMVar_hsa_circ_87310,RMVar_hsa_circ_122969,RMVar_hsa_circ_169178,RMVar_hsa_circ_169186,RMVar_hsa_circ_90357,RMVar_hsa_circ_169198,RMVar_hsa_circ_99123,RMVar_hsa_circ_169207,RMVar_hsa_circ_105884,RMVar_hsa_circ_169229,RMVar_hsa_circ_76343,RMVar_hsa_circ_169230,RMVar_hsa_circ_98599,RMVar_hsa_circ_169241,RMVar_hsa_circ_97684,RMVar_hsa_circ_94660,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_125165,RMVar_hsa_circ_169258,RMVar_hsa_circ_125913,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169262,RMVar_hsa_circ_115030,RMVar_hsa_circ_169270,RMVar_hsa_circ_88408,RMVar_hsa_circ_169280,RMVar_hsa_circ_103111,RMVar_hsa_circ_169284,RMVar_hsa_circ_113073,RMVar_hsa_circ_122984,RMVar_hsa_circ_169285,RMVar_hsa_circ_169286,RMVar_hsa_circ_85124,RMVar_hsa_circ_169294,RMVar_hsa_circ_87538,RMVar_hsa_circ_169303,RMVar_hsa_circ_127230,RMVar_hsa_circ_169308,RMVar_hsa_circ_110513,RMVar_hsa_circ_169309,RMVar_hsa_circ_78327,RMVar_hsa_circ_169318,RMVar_hsa_circ_115331,RMVar_hsa_circ_169321,RMVar_hsa_circ_67978,RMVar_hsa_circ_108051,RMVar_hsa_circ_169330,RMVar_hsa_circ_371950,RMVar_hsa_circ_13373,RMVar_hsa_circ_102947,RMVar_hsa_circ_169332,RMVar_hsa_circ_71435,RMVar_hsa_circ_77105,RMVar_hsa_circ_169335,RMVar_hsa_circ_169336,RMVar_hsa_circ_84052,RMVar_hsa_circ_169340,RMVar_hsa_circ_99163,RMVar_hsa_circ_109553,RMVar_hsa_circ_89122,RMVar_hsa_circ_119659,RMVar_hsa_circ_169344,RMVar_hsa_circ_309417,RMVar_hsa_circ_305008,RMVar_hsa_circ_122476,RMVar_hsa_circ_102150,RMVar_hsa_circ_112281,RMVar_hsa_circ_100906,RMVar_hsa_circ_169348,RMVar_hsa_circ_169350,RMVar_hsa_circ_169352,RMVar_hsa_circ_169353,RMVar_hsa_circ_169351,RMVar_hsa_circ_169349,RMVar_hsa_circ_169346,RMVar_hsa_circ_169347,RMVar_hsa_circ_374899,RMVar_hsa_circ_58457,RMVar_hsa_circ_93355,RMVar_hsa_circ_101603,RMVar_hsa_circ_82211,RMVar_hsa_circ_169357,RMVar_hsa_circ_169359,RMVar_hsa_circ_169360,RMVar_hsa_circ_169358,RMVar_hsa_circ_169356 61048 RMVar_ID_61048 Human_SNP_ID_567718397 m1A Human chr14 - 102046431 102046431 102046431 GCCTGGCTTTGGCTTTCCCTCCAGACCCGCCCAGCTCGCCTGGCTTATCCCTCCTGATTCTGTCC GCCTGGCTTTGGCTTTCCCTCCAGACCCGCCCTGCTCGCCTGGCTTATCCCTCCTGATTCTGTCC T A AL118558.1 Ensembl:ENSG00000258959 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102046430..102046498 26863196 MeRIP-seq:(Medium) rs1420597355 Functional Loss SNV dbSNP153 33..33 33 - - - 61049 RMVar_ID_61049 Human_SNP_ID_567721490 m1A Human chr14 - 102055741 102055739 102055742 ATCAGCTGCCTGCGGGGTTTGGAAGGAGGAGGAGCCAGGGCCTTGGGAAACATTTCAGCCTGAGC ATCAGCTGCCTGCGGGGTTTGGAAGGAGGAG___CCAGGGCCTTGGGAAACATTTCAGCCTGAGC GCTC G AL118558.1 Ensembl:ENSG00000258959 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102055727..102055849 26863196 MeRIP-seq:(Medium) rs754079226 Functional Loss DEL dbSNP153 32..34 33 - - - 61050 RMVar_ID_61050 Human_SNP_ID_567729752 m1A Human chr14 - 102081171 102081171 102081171 AAAGAAAAGTATTGTTTGGAGGAGCAAAGTTAAAAGCCTACCTAAGCATATCGTAAAGCTGTTCA AAAGAAAAGTATTGTTTGGAGGAGCAAAGTTAGAAGCCTACCTAAGCATATCGTAAAGCTGTTCA T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102081120..102081200 26863196 MeRIP-seq:(Medium) rs575140426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38884,Human_RBP_ID_441349,Human_RBP_ID_997495,Human_RBP_ID_1170938,Human_RBP_ID_1273715,Human_RBP_ID_1487928,Human_RBP_ID_1814588,Human_RBP_ID_2405365,Human_RBP_ID_3441576,Human_RBP_ID_5438811,Human_RBP_ID_6324522,Human_RBP_ID_8398904,Human_RBP_ID_12270871,Human_RBP_ID_17246477,Human_RBP_ID_17361375,Human_RBP_ID_17478243,Human_RBP_ID_17651754,Human_RBP_ID_17686810,Human_RBP_ID_17856764,Human_RBP_ID_18271693,Human_RBP_ID_18645111,Human_RBP_ID_22797027,Human_RBP_ID_23611600,Human_RBP_ID_26432225,Human_RBP_ID_26920177,Human_RBP_ID_27223758,Human_RBP_ID_27642944 Human_miRNA_ID_2970662,Human_miRNA_ID_2970663 RMVar_hsa_circ_96094,RMVar_hsa_circ_117634,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_127877,RMVar_hsa_circ_119531,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_87280,RMVar_hsa_circ_169376,RMVar_hsa_circ_169378,RMVar_hsa_circ_169379,RMVar_hsa_circ_169377,RMVar_hsa_circ_169375,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369 61051 RMVar_ID_61051 Human_SNP_ID_567729753 m1A Human chr14 - 102081171 102081171 102081171 AAAGAAAAGTATTGTTTGGAGGAGCAAAGTTAAAAGCCTACCTAAGCATATCGTAAAGCTGTTCA AAAGAAAAGTATTGTTTGGAGGAGCAAAGTTACAAGCCTACCTAAGCATATCGTAAAGCTGTTCA T G HSP90AA1 Ensembl:ENSG00000080824 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102081120..102081200 26863196 MeRIP-seq:(Medium) rs575140426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38884,Human_RBP_ID_441349,Human_RBP_ID_997495,Human_RBP_ID_1170938,Human_RBP_ID_1273715,Human_RBP_ID_1487928,Human_RBP_ID_1814588,Human_RBP_ID_2405365,Human_RBP_ID_3441576,Human_RBP_ID_5438811,Human_RBP_ID_6324522,Human_RBP_ID_8398904,Human_RBP_ID_12270871,Human_RBP_ID_17246477,Human_RBP_ID_17361375,Human_RBP_ID_17478243,Human_RBP_ID_17651754,Human_RBP_ID_17686810,Human_RBP_ID_17856764,Human_RBP_ID_18271693,Human_RBP_ID_18645111,Human_RBP_ID_22797027,Human_RBP_ID_23611600,Human_RBP_ID_26432225,Human_RBP_ID_26920177,Human_RBP_ID_27223758,Human_RBP_ID_27642944 Human_miRNA_ID_2970662,Human_miRNA_ID_2970663 RMVar_hsa_circ_96094,RMVar_hsa_circ_117634,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_127877,RMVar_hsa_circ_119531,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_87280,RMVar_hsa_circ_169376,RMVar_hsa_circ_169378,RMVar_hsa_circ_169379,RMVar_hsa_circ_169377,RMVar_hsa_circ_169375,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369 61052 RMVar_ID_61052 Human_SNP_ID_567730303 m1A Human chr14 - 102082418 102082418 102082418 TTACAGGTGGTTGTGTCAAACCGATTGGTGACATCTCCATGCTGTATTGTCACAAGCACATATGG TTACAGGTGGTTGTGTCAAACCGATTGGTGACCTCTCCATGCTGTATTGTCACAAGCACATATGG T G HSP90AA1 Ensembl:ENSG00000080824 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102082080..102082423 26863196 MeRIP-seq:(Medium) rs750025022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196957,Human_RBP_ID_441381,Human_RBP_ID_880680,Human_RBP_ID_997508,Human_RBP_ID_1487952,Human_RBP_ID_1814601,Human_RBP_ID_2432118,Human_RBP_ID_3441594,Human_RBP_ID_3945115,Human_RBP_ID_4281910,Human_RBP_ID_5112471,Human_RBP_ID_5141031,Human_RBP_ID_5463752,Human_RBP_ID_5523097,Human_RBP_ID_6324568,Human_RBP_ID_8230574,Human_RBP_ID_8398929,Human_RBP_ID_8792779,Human_RBP_ID_9039417,Human_RBP_ID_9256292,Human_RBP_ID_9281402,Human_RBP_ID_9345165,Human_RBP_ID_9369443,Human_RBP_ID_12270933,Human_RBP_ID_17187213,Human_RBP_ID_17246496,Human_RBP_ID_17361387,Human_RBP_ID_17478261,Human_RBP_ID_17651252,Human_RBP_ID_17856515,Human_RBP_ID_18189528,Human_RBP_ID_18418298,Human_RBP_ID_18469520,Human_RBP_ID_18544276,Human_RBP_ID_18645140,Human_RBP_ID_18979891,Human_RBP_ID_20001262,Human_RBP_ID_21969577,Human_RBP_ID_22044683,Human_RBP_ID_22183273,Human_RBP_ID_22439467,Human_RBP_ID_22472982,Human_RBP_ID_22648631,Human_RBP_ID_22797046,Human_RBP_ID_23611625,Human_RBP_ID_24558198,Human_RBP_ID_26324743,Human_RBP_ID_26920191,Human_RBP_ID_27642957,Human_RBP_ID_27808557 Human_Splice_Rec_1556704,Human_Splice_Rec_1556726 Human_miRNA_ID_1985078,Human_miRNA_ID_1985079,Human_miRNA_ID_2940716,Human_miRNA_ID_2940717 RMVar_hsa_circ_96094,RMVar_hsa_circ_117634,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_127877,RMVar_hsa_circ_119531,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_169376,RMVar_hsa_circ_169378,RMVar_hsa_circ_169377,RMVar_hsa_circ_169375,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_169381,RMVar_hsa_circ_83063,RMVar_hsa_circ_329287,RMVar_hsa_circ_169380 61053 RMVar_ID_61053 Human_SNP_ID_567730660 m1A Human chr14 - 102083131 102083131 102083131 GTCAGTCACCAAAGAAGGCCTGGAACTTCCAGAGGATGAAGAAGAGAAAAAGAAGCAGGAAGAGA GTCAGTCACCAAAGAAGGCCTGGAACTTCCAGCGGATGAAGAAGAGAAAAAGAAGCAGGAAGAGA T G HSP90AA1 Ensembl:ENSG00000080824 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102083081..102083229 26863196 MeRIP-seq:(Medium) rs927888850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38897,Human_RBP_ID_230915,Human_RBP_ID_441383,Human_RBP_ID_756641,Human_RBP_ID_812670,Human_RBP_ID_882689,Human_RBP_ID_1065835,Human_RBP_ID_1487959,Human_RBP_ID_1814608,Human_RBP_ID_2432122,Human_RBP_ID_3441595,Human_RBP_ID_4281917,Human_RBP_ID_6324572,Human_RBP_ID_8230575,Human_RBP_ID_8249958,Human_RBP_ID_8398936,Human_RBP_ID_8792782,Human_RBP_ID_9369450,Human_RBP_ID_12270943,Human_RBP_ID_17246497,Human_RBP_ID_17361388,Human_RBP_ID_17478262,Human_RBP_ID_17844693,Human_RBP_ID_18161114,Human_RBP_ID_18435509,Human_RBP_ID_18528165,Human_RBP_ID_18645146,Human_RBP_ID_19064380,Human_RBP_ID_19913109,Human_RBP_ID_22042375,Human_RBP_ID_22183281,Human_RBP_ID_22797048,Human_RBP_ID_23611627,Human_RBP_ID_24367286,Human_RBP_ID_24470763,Human_RBP_ID_24543734,Human_RBP_ID_26324747,Human_RBP_ID_26920199,Human_RBP_ID_27223776,Human_RBP_ID_27808563 Human_Splice_Rec_1556703,Human_Splice_Rec_1556725 RMVar_hsa_circ_74031,RMVar_hsa_circ_96094,RMVar_hsa_circ_117634,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_127877,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_169376,RMVar_hsa_circ_169377,RMVar_hsa_circ_169375,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_83063,RMVar_hsa_circ_169380,RMVar_hsa_circ_16211 61054 RMVar_ID_61054 Human_SNP_ID_567731394 m1A Human chr14 - 102084514 102084514 102084514 CAGTTGGAATTCAGAGCCCTTCTATTTGTCCCACGACGTGCTCCTTTTGATCTGTTTGAAAACAG CAGTTGGAATTCAGAGCCCTTCTATTTGTCCCGCGACGTGCTCCTTTTGATCTGTTTGAAAACAG T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102084416..102084517 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_38909,Human_RBP_ID_230916,Human_RBP_ID_441390,Human_RBP_ID_756646,Human_RBP_ID_997514,Human_RBP_ID_1236824,Human_RBP_ID_1273725,Human_RBP_ID_1360771,Human_RBP_ID_1487978,Human_RBP_ID_1814626,Human_RBP_ID_2432128,Human_RBP_ID_3441609,Human_RBP_ID_4281941,Human_RBP_ID_5353344,Human_RBP_ID_6324601,Human_RBP_ID_8398954,Human_RBP_ID_8792799,Human_RBP_ID_9039421,Human_RBP_ID_9281409,Human_RBP_ID_9369468,Human_RBP_ID_17246503,Human_RBP_ID_17478273,Human_RBP_ID_17844697,Human_RBP_ID_18161116,Human_RBP_ID_18189444,Human_RBP_ID_18271708,Human_RBP_ID_18645166,Human_RBP_ID_22183297,Human_RBP_ID_22797059,Human_RBP_ID_23611638,Human_RBP_ID_24367287,Human_RBP_ID_24543741,Human_RBP_ID_26622696,Human_RBP_ID_26920216,Human_RBP_ID_27223788,Human_RBP_ID_27429451,Human_RBP_ID_27642964 Human_Splice_Rec_1556696,Human_Splice_Rec_1556718,Human_Splice_Rec_1556734 RMVar_hsa_circ_74031,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_83063,RMVar_hsa_circ_169380,RMVar_hsa_circ_16211,RMVar_hsa_circ_301740,RMVar_hsa_circ_63125,RMVar_hsa_circ_169382,RMVar_hsa_circ_50191 61055 RMVar_ID_61055 Human_SNP_ID_567731677 m1A Human chr14 - 102084979 102084977 102084980 TTTTCTTTTGAAGGTGGAGAAGGAACGTGATAAAGAAGTAAGCGATGATGAGGCTGAAGAAAAGG TTTTCTTTTGAAGGTGGAGAAGGAACGTGAT___GAAGTAAGCGATGATGAGGCTGAAGAAAAGG CTTT C HSP90AA1 Ensembl:ENSG00000080824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:102084701..102085446 32194978 MeRIP-seq:(Medium) rs746607033 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_38913,Human_RBP_ID_197162,Human_RBP_ID_230919,Human_RBP_ID_812767,Human_RBP_ID_1487990,Human_RBP_ID_1814634,Human_RBP_ID_3441615,Human_RBP_ID_4281951,Human_RBP_ID_6324616,Human_RBP_ID_8249974,Human_RBP_ID_8792808,Human_RBP_ID_9039422,Human_RBP_ID_9345167,Human_RBP_ID_9369474,Human_RBP_ID_12270984,Human_RBP_ID_17246508,Human_RBP_ID_17361397,Human_RBP_ID_17478281,Human_RBP_ID_18528178,Human_RBP_ID_18544279,Human_RBP_ID_18645176,Human_RBP_ID_19066052,Human_RBP_ID_22042388,Human_RBP_ID_22758401,Human_RBP_ID_22921153,Human_RBP_ID_23113680,Human_RBP_ID_23611640,Human_RBP_ID_24543760,Human_RBP_ID_25123686,Human_RBP_ID_26325476,Human_RBP_ID_27808584 Human_Splice_Rec_1556694,Human_Splice_Rec_1556716,Human_Splice_Rec_1556732,Human_Splice_Rec_1556752,Human_Splice_Rec_1556754 RMVar_hsa_circ_74031,RMVar_hsa_circ_120437,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_87088,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_83063,RMVar_hsa_circ_169380,RMVar_hsa_circ_16211,RMVar_hsa_circ_301740,RMVar_hsa_circ_63125,RMVar_hsa_circ_169382,RMVar_hsa_circ_50191 61056 RMVar_ID_61056 Human_SNP_ID_567732107 m1A Human chr14 + 102085733 102085733 102085733 GTTGCAGCACCCCACCCTTCCACCGCTCACTTAACCAGTGAATGTTCAGGTGCCTACCTGTGTCT GTTGCAGCACCCCACCCTTCCACCGCTCACTTCACCAGTGAATGTTCAGGTGCCTACCTGTGTCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102085731..102085886 26863196 MeRIP-seq:(Medium) rs749997138 Functional Loss SNV dbSNP153 33..33 33 - - - 61057 RMVar_ID_61057 Human_SNP_ID_567732108 m1A Human chr14 + 102085733 102085733 102085733 GTTGCAGCACCCCACCCTTCCACCGCTCACTTAACCAGTGAATGTTCAGGTGCCTACCTGTGTCT GTTGCAGCACCCCACCCTTCCACCGCTCACTTTACCAGTGAATGTTCAGGTGCCTACCTGTGTCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102085731..102085886 26863196 MeRIP-seq:(Medium) rs749997138 Functional Loss SNV dbSNP153 33..33 33 - - - 61058 RMVar_ID_61058 Human_SNP_ID_567732150 m1A Human chr14 + 102085804 102085804 102085804 ACTGTGAATGATCCCCCTGCTGAGGACTCCCAAGCGTACTGCTCATCATCGTTATGTTTGGTGAT ACTGTGAATGATCCCCCTGCTGAGGACTCCCACGCGTACTGCTCATCATCGTTATGTTTGGTGAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102085718..102085886 26863196 MeRIP-seq:(Medium) rs772787983 Functional Loss SNV dbSNP153 33..33 33 - - - 61059 RMVar_ID_61059 Human_SNP_ID_567732151 m1A Human chr14 + 102085804 102085804 102085804 ACTGTGAATGATCCCCCTGCTGAGGACTCCCAAGCGTACTGCTCATCATCGTTATGTTTGGTGAT ACTGTGAATGATCCCCCTGCTGAGGACTCCCAGGCGTACTGCTCATCATCGTTATGTTTGGTGAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102085718..102085886 26863196 MeRIP-seq:(Medium) rs772787983 Functional Loss SNV dbSNP153 33..33 33 - - - 61060 RMVar_ID_61060 Human_SNP_ID_567732179 m1A Human chr14 + 102085852 102085852 102085852 TCGTTATGTTTGGTGATCACAGTTACTTTCTCAGCAACCAAATAAGCAGAATAAAAACCAACACC TCGTTATGTTTGGTGATCACAGTTACTTTCTCTGCAACCAAATAAGCAGAATAAAAACCAACACC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102085801..102085884 26863196 MeRIP-seq:(Medium) rs1301877431 Functional Loss SNV dbSNP153 33..33 33 - - - 61061 RMVar_ID_61061 Human_SNP_ID_567732443 m1A Human chr14 - 102086380 102086380 102086380 TGCAAGGTTTTAAACCGGCGCGGTGTCGTTCCAGATGCCTGAGGAAACCCAGACCCAAGACCAAC TGCAAGGTTTTAAACCGGCGCGGTGTCGTTCCGGATGCCTGAGGAAACCCAGACCCAAGACCAAC T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102086376..102086400 32194978 MeRIP-seq:(Medium) rs375119946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882701,Human_RBP_ID_3441628,Human_RBP_ID_19064386,Human_RBP_ID_22577938,Human_RBP_ID_22648638,Human_RBP_ID_26778526 RMVar_hsa_circ_102877,RMVar_hsa_circ_87088,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_16211 61062 RMVar_ID_61062 Human_SNP_ID_567732570 m1A Human chr14 - 102086564 102086564 102086564 CGGGCCTGCGGCGGCCTCCCGGAAGCGCGCACACGCTCGTGGTAGTTGCCGCGCTCCGAAATGAG CGGGCCTGCGGCGGCCTCCCGGAAGCGCGCACCCGCTCGTGGTAGTTGCCGCGCTCCGAAATGAG T G HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102086562..102086665 26863196 MeRIP-seq:(Medium) rs534522717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087621,Human_RBP_ID_9417958,Human_RBP_ID_22415045 RMVar_hsa_circ_102877,RMVar_hsa_circ_87088,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_16211 61063 RMVar_ID_61063 Human_SNP_ID_567732673 m1A Human chr14 - 102086754 102086754 102086754 CCGCGGGCTCCCCGAGGCTCTGCAGCAGCGCCAGAGCTGGCGCCGCACGCGAACAGAGCGGCCCC CCGCGGGCTCCCCGAGGCTCTGCAGCAGCGCCGGAGCTGGCGCCGCACGCGAACAGAGCGGCCCC T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102086751..102087561 26863196 MeRIP-seq:(Medium) rs1376122147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18480440,Human_RBP_ID_18645197 RMVar_hsa_circ_102877,RMVar_hsa_circ_87088,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_16211 61064 RMVar_ID_61064 Human_SNP_ID_567732785 m1A Human chr14 + 102086977 102086977 102086977 TCCCCAGTCCACCTCCACAGGCCCCCACAACCACCCGTCACCTTGGCTAAGTGACCGCACAGGAC TCCCCAGTCCACCTCCACAGGCCCCCACAACCCCCCGTCACCTTGGCTAAGTGACCGCACAGGAC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr14:102086976..102087050;chr14:102086976..102087025 26863196,32194978 MeRIP-seq:(Medium) rs1357149681 Functional Loss SNV dbSNP153 33..33 33 - - - 61065 RMVar_ID_61065 Human_SNP_ID_567732788 m1A Human chr14 - 102086982 102086982 102086982 CGTTGGTCCTGTGCGGTCACTTAGCCAAGGTGACGGGTGGTTGTGGGGGCCTGTGGAGGTGGACT CGTTGGTCCTGTGCGGTCACTTAGCCAAGGTGTCGGGTGGTTGTGGGGGCCTGTGGAGGTGGACT T A HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:102086976..102087075 26863196 MeRIP-seq:(Medium) rs1328770206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1273729,Human_RBP_ID_19064388,Human_RBP_ID_22578840 RMVar_hsa_circ_102877,RMVar_hsa_circ_87088,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369,RMVar_hsa_circ_16211 61066 RMVar_ID_61066 Human_SNP_ID_567733073 m1A Human chr14 + 102087449 102087449 102087449 GTGGGGGCCTTTGAAGTGAGGTGTAGTTGGTCACCCGGGCTGAGCGGAACGCGGGGCCGGGGTGG GTGGGGGCCTTTGAAGTGAGGTGTAGTTGGTCGCCCGGGCTGAGCGGAACGCGGGGCCGGGGTGG A G lnc-DYNC1H1-6 RNACentral:URS0000D590B8 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102087398..102087508 26863196 MeRIP-seq:(Medium) rs1488141209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12271014 61067 RMVar_ID_61067 Human_SNP_ID_567747218 m1A Human chr14 + 102139934 102139934 102139934 AGGATGAACGCTGCTTTCCAAGATGGCGACGGAGGGAGGAGGGAAGGAGATGAACGAGATTAAGA AGGATGAACGCTGCTTTCCAAGATGGCGACGGGGGGAGGAGGGAAGGAGATGAACGAGATTAAGA A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102139906..102140026 26863196 MeRIP-seq:(Medium) rs767616468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4282009,Human_RBP_ID_6406062,Human_RBP_ID_9370481,Human_RBP_ID_22044690,Human_RBP_ID_22921173 Human_Splice_Rec_1556817 61068 RMVar_ID_61068 Human_SNP_ID_567773879 m1A Human chr14 - 102240836 102240836 102240836 TGCCCATAGTGAAGCAGGCAAGCCCAGAGAAAAGAGAGGGTAGAGACACAGATAAGGAGGGTGGT TGCCCATAGTGAAGCAGGCAAGCCCAGAGAAACGAGAGGGTAGAGACACAGATAAGGAGGGTGGT T G MOK Ensembl:ENSG00000080823 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102240807..102240934 26863196 MeRIP-seq:(Medium) rs907268168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41104,RMVar_hsa_circ_344740,RMVar_hsa_circ_36672 61069 RMVar_ID_61069 Human_SNP_ID_567773962 m1A Human chr14 - 102241225 102241225 102241225 AGGGGTCAGATGGGTCTGTAGAAAAGGATTCAAAGGACTCAGAGCTTGGAGTGGAGACTGAAGGA AGGGGTCAGATGGGTCTGTAGAAAAGGATTCAGAGGACTCAGAGCTTGGAGTGGAGACTGAAGGA T C MOK Ensembl:ENSG00000080823 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102241195..102241268 26863196 MeRIP-seq:(Medium) rs1162245827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41104,RMVar_hsa_circ_344740,RMVar_hsa_circ_36672 61070 RMVar_ID_61070 Human_SNP_ID_567794860 m1A Human chr14 - 102319831 102319831 102319831 ACACGTGCGACGCTGCCGCTCTGGCCCGGAGGAGCCGGGCCGCCGCCGCCGCCGCCATCCTCGCT ACACGTGCGACGCTGCCGCTCTGGCCCGGAGGGGCCGGGCCGCCGCCGCCGCCGCCATCCTCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:102319781..102319866;chr14:102319780..102320173 26863196 MeRIP-seq:(Medium) rs1412081242 Functional Loss SNV dbSNP153 33..33 33 - - - 61071 RMVar_ID_61071 Human_SNP_ID_567796580 m1A Human chr14 + 102326368 102326368 102326368 CCGCTGGCAGTAACATCTCTTTCATCCAGTTCAGCACATCCATTTATTTCCAACTTGCATACAAG CCGCTGGCAGTAACATCTCTTTCATCCAGTTCTGCACATCCATTTATTTCCAACTTGCATACAAG A T ZNF839 Ensembl:ENSG00000022976 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:102326318..102326419 32194978 MeRIP-seq:(Medium) rs1206552236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17478292,Human_RBP_ID_18645310 RMVar_hsa_circ_169394,RMVar_hsa_circ_5739,RMVar_hsa_circ_272363,RMVar_hsa_circ_300202,RMVar_hsa_circ_370943,RMVar_hsa_circ_286331,RMVar_hsa_circ_77593,RMVar_hsa_circ_169396,RMVar_hsa_circ_169397,RMVar_hsa_circ_169398,RMVar_hsa_circ_169395 61072 RMVar_ID_61072 Human_SNP_ID_567802784 m1A Human chr14 + 102348410 102348410 102348410 GCCGCGGGTTGTGGGCATGAGCACGCCTGGAGAGGCCATGGGGCTGGTGACAAGCTCTGGCCAGA GCCGCGGGTTGTGGGCATGAGCACGCCTGGAGGGGCCATGGGGCTGGTGACAAGCTCTGGCCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:102348360..102348464;chr14:102348366..102348468 26863196 MeRIP-seq:(Medium) rs892907457 Functional Loss SNV dbSNP153 33..33 33 - - - 61073 RMVar_ID_61073 Human_SNP_ID_567802807 m1A Human chr14 - 102348472 102348472 102348472 AGTCTGCCTAGGACCCAGTGCCGCAGGCCTGGATCAGACCCCAGGATCAGACCTTGGGGTCTTCT AGTCTGCCTAGGACCCAGTGCCGCAGGCCTGGCTCAGACCCCAGGATCAGACCTTGGGGTCTTCT T G CINP Ensembl:ENSG00000100865 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102348377..102348478 32194978 MeRIP-seq:(Medium) rs1176194358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_441456,Human_RBP_ID_22797087,Human_RBP_ID_26808303 Human_miRNA_ID_253635 RMVar_hsa_circ_74676,RMVar_hsa_circ_342880,RMVar_hsa_circ_317324,RMVar_hsa_circ_169401 61074 RMVar_ID_61074 Human_SNP_ID_567807308 m1A Human chr14 + 102367072 102367072 102367072 CAGAGTGGGTCAGTGGAGCTAGAACTTGGAGGACAAGTGGAGACGGGTAGAGAGGTGACAGGGGA CAGAGTGGGTCAGTGGAGCTAGAACTTGGAGGGCAAGTGGAGACGGGTAGAGAGGTGACAGGGGA A G TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102367021..102367122 26863196 MeRIP-seq:(Medium) rs765805924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12273769 61075 RMVar_ID_61075 Human_SNP_ID_567820131 m1A Human chr14 + 102417983 102417983 102417983 AGCCGCAGGGAGGCTGCCTTGGGAGTCCAGGGAAACCATTGACTGAGATGGAGACTGGAGACTGG AGCCGCAGGGAGGCTGCCTTGGGAGTCCAGGGCAACCATTGACTGAGATGGAGACTGGAGACTGG A C TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102417967..102418099 26863196 MeRIP-seq:(Medium) rs1362777597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1036,RMVar_hsa_circ_45553,RMVar_hsa_circ_314981,RMVar_hsa_circ_288761,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_169406,RMVar_hsa_circ_317442,RMVar_hsa_circ_22690,RMVar_hsa_circ_169408,RMVar_hsa_circ_45590,RMVar_hsa_circ_127684,RMVar_hsa_circ_169409 61076 RMVar_ID_61076 Human_SNP_ID_567824578 m1A Human chr14 + 102434600 102434600 102434600 GAGCGAGGGAAGATGTGGGAGGCAGTGATGTCACGGGACTCGGAGATGAGCCGTGTCCTGCAGAT GAGCGAGGGAAGATGTGGGAGGCAGTGATGTCCCGGGACTCGGAGATGAGCCGTGTCCTGCAGAT A C TECPR2 Ensembl:ENSG00000196663 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102434552..102434656 26863196 MeRIP-seq:(Medium) rs1405050229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2722378 RMVar_hsa_circ_45553,RMVar_hsa_circ_288761,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_22690,RMVar_hsa_circ_17853,RMVar_hsa_circ_45590,RMVar_hsa_circ_127684,RMVar_hsa_circ_309868,RMVar_hsa_circ_169409,RMVar_hsa_circ_347375,RMVar_hsa_circ_315379,RMVar_hsa_circ_72494,RMVar_hsa_circ_169410,RMVar_hsa_circ_361063,RMVar_hsa_circ_364629,RMVar_hsa_circ_266060,RMVar_hsa_circ_294786,RMVar_hsa_circ_105862,RMVar_hsa_circ_169412,RMVar_hsa_circ_169413,RMVar_hsa_circ_169414 61077 RMVar_ID_61077 Human_SNP_ID_567840944 m1A Human chr14 + 102498888 102498867 102498889 CACACCACAACACACAACACACCTCACCTCACACCACAGCACACCTCACCACACCACACCGCACT CACACCACAACA______________________CACAGCACACCTCACCACACCACACCGCACT ACACAACACACCTCACCTCACAC A TECPR2 Ensembl:ENSG00000196663 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102498844..102499030 26863196 MeRIP-seq:(Medium) rs1159653504 Functional Loss DEL dbSNP153 13..34 33 - - - Human_RBP_ID_197281 RMVar_hsa_circ_266510 61078 RMVar_ID_61078 Human_SNP_ID_567842951 m1A Human chr14 - 102506590 102506590 102506590 GGGTGGGGACTGGCATGTCCAAGCAGCAGGACAGCGTATAAAAAGGCCTGGAAGCCAAGAGAACG GGGTGGGGACTGGCATGTCCAAGCAGCAGGACGGCGTATAAAAAGGCCTGGAAGCCAAGAGAACG T C ANKRD9 Ensembl:ENSG00000156381 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102506540..102506615 26863196 MeRIP-seq:(Medium) rs183437621 Functional Loss SNV dbSNP153 33..33 33 - - - 61079 RMVar_ID_61079 Human_SNP_ID_567843198 m1A Human chr14 - 102507273 102507273 102507273 TCTCGAGCTGCTGCTGCGCCAGCTGGGCCGCGACGCCGGGGCCACTCCCTCCGCCGCCGGAGCCC TCTCGAGCTGCTGCTGCGCCAGCTGGGCCGCGTCGCCGGGGCCACTCCCTCCGCCGCCGGAGCCC T A ANKRD9 Ensembl:ENSG00000156381 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:102507082..102507382 26863410 MeRIP-seq:(Medium) rs1411575974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8798315,Human_RBP_ID_9323887,Human_RBP_ID_22532587 61080 RMVar_ID_61080 Human_SNP_ID_567843463 m1A Human chr14 + 102507866 102507866 102507866 GAGGCCTCGGGCCCGCCGTCCGCGCCACCCCCAGGCCGCCGCGCGTCCCACGGCATGCTGGCGGC GAGGCCTCGGGCCCGCCGTCCGCGCCACCCCCCGGCCGCCGCGCGTCCCACGGCATGCTGGCGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102507822..102507893 26863196 MeRIP-seq:(Medium) rs1222914542 Functional Loss SNV dbSNP153 33..33 33 - - - 61081 RMVar_ID_61081 Human_SNP_ID_567862536 m1A Human chr14 - 102575760 102575760 102575760 CATTCCCGCCAGCATTCTGGTCATTATCACTTAAGCAATCTCTAAGAAGTTTTCCACTCTCCCTG CATTCCCGCCAGCATTCTGGTCATTATCACTTGAGCAATCTCTAAGAAGTTTTCCACTCTCCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102575732..102575838 26863196 MeRIP-seq:(Medium) rs1003763240 Functional Loss SNV dbSNP153 33..33 33 - - - 61082 RMVar_ID_61082 Human_SNP_ID_567867526 m1A Human chr14 - 102592697 102592697 102592697 GAGCGCGGAGCCGCTTCAAGCCCCCAGCGACGAGCCGAGCGCAACTTTCGCTCTCATCGCCGCCC GAGCGCGGAGCCGCTTCAAGCCCCCAGCGACGGGCCGAGCGCAACTTTCGCTCTCATCGCCGCCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:102592651..102593150 26863196 MeRIP-seq:(Medium) rs1454396568 Functional Loss SNV dbSNP153 33..33 33 - - - 61083 RMVar_ID_61083 Human_SNP_ID_567867555 m1A Human chr14 - 102592768 102592768 102592768 GGCGCGGGGCCGGGCGGGCGCGGCGGGAGCCCACGGGCGCGAGTCCGAGTCGGGGGAGGCCCAAA GGCGCGGGGCCGGGCGGGCGCGGCGGGAGCCCGCGGGCGCGAGTCCGAGTCGGGGGAGGCCCAAA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:102592710..102593107 26863410 MeRIP-seq:(Medium) rs999271685 Functional Loss SNV dbSNP153 33..33 33 - - - 61084 RMVar_ID_61084 Human_SNP_ID_567867558 m1A Human chr14 - 102592773 102592773 102592773 GGGCCGGCGCGGGGCCGGGCGGGCGCGGCGGGAGCCCACGGGCGCGAGTCCGAGTCGGGGGAGGC GGGCCGGCGCGGGGCCGGGCGGGCGCGGCGGGGGCCCACGGGCGCGAGTCCGAGTCGGGGGAGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:102592710..102592859 26863410 MeRIP-seq:(Medium) rs1187256720 Functional Loss SNV dbSNP153 33..33 33 - - - 61085 RMVar_ID_61085 Human_SNP_ID_567867572 m1A Human chr14 - 102592815 102592815 102592815 CGGCTCCTGAGGAGGGGGCGCCGAGACGGGGGAGGGGGCGCGGGGCCGGCGCGGGGCCGGGCGGG CGGCTCCTGAGGAGGGGGCGCCGAGACGGGGGGGGGGGCGCGGGGCCGGCGCGGGGCCGGGCGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr14:102592651..102681903;chr14:102592707..102592953 26863196 MeRIP-seq:(Medium) rs1398932001 Functional Loss SNV dbSNP153 33..33 33 - - - 61086 RMVar_ID_61086 Human_SNP_ID_567867758 m1A Human chr14 - 102593040 102593037 102593040 GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGGAGGCGGCGGCGCCCGAGGCGGCAGTGGCGGCTG GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGG___CGGCGGCGCCCGAGGCGGCAGTGGCGGCTG GCCT G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:102592710..102593058 26863410 MeRIP-seq:(Medium) rs908905035 Functional Loss DEL dbSNP153 33..35 33 - - - 61087 RMVar_ID_61087 Human_SNP_ID_567867761 m1A Human chr14 - 102593040 102593040 102593040 GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGGAGGCGGCGGCGCCCGAGGCGGCAGTGGCGGCTG GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGGTGGCGGCGGCGCCCGAGGCGGCAGTGGCGGCTG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:102592710..102593058 26863410 MeRIP-seq:(Medium) rs1372120045 Functional Loss SNV dbSNP153 33..33 33 - - - 61088 RMVar_ID_61088 Human_SNP_ID_567867762 m1A Human chr14 - 102593040 102593040 102593040 GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGGAGGCGGCGGCGCCCGAGGCGGCAGTGGCGGCTG GGCGGCTGAGGCGGCGGCGGCCGAGGCTGAGGCGGCGGCGGCGCCCGAGGCGGCAGTGGCGGCTG T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:102592710..102593058 26863410 MeRIP-seq:(Medium) rs1372120045 Functional Loss SNV dbSNP153 33..33 33 - - - 61089 RMVar_ID_61089 Human_SNP_ID_567920057 m1A Human chr14 - 102777232 102777231 102777232 TAGCAACGGCGGCGCCGCGGCGCGGGGCGGGGACGGCCCCGGGCGCCCCCCGCCTCCCTCCCGTC TAGCAACGGCGGCGCCGCGGCGCGGGGCGGGG_CGGCCCCGGGCGCCCCCCGCCTCCCTCCCGTC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:102777201..102777307;chr14:102777198..102777323 26863196 MeRIP-seq:(Medium) rs1031621809 Functional Loss DEL dbSNP153 33..33 33 - - - 61090 RMVar_ID_61090 Human_SNP_ID_567920058 m1A Human chr14 - 102777232 102777232 102777232 TAGCAACGGCGGCGCCGCGGCGCGGGGCGGGGACGGCCCCGGGCGCCCCCCGCCTCCCTCCCGTC TAGCAACGGCGGCGCCGCGGCGCGGGGCGGGGGCGGCCCCGGGCGCCCCCCGCCTCCCTCCCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:102777201..102777307;chr14:102777198..102777323 26863196 MeRIP-seq:(Medium) rs974185237 Functional Loss SNV dbSNP153 33..33 33 - - - 61091 RMVar_ID_61091 Human_SNP_ID_567921005 m1A Human chr14 + 102780133 102780129 102780133 AGGCCAGAGGATTTGGAAGGCTACCAGAGAGAAGCAGCCGAGGCCTGATTGTGGAAATGATGCTT AGGCCAGAGGATTTGGAAGGCTACCAGAG____GCAGCCGAGGCCTGATTGTGGAAATGATGCTT GAGAA G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102780127..102780207 26863196 MeRIP-seq:(Medium) rs1310093398 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 61092 RMVar_ID_61092 Human_SNP_ID_567921008 m1A Human chr14 + 102780133 102780133 102780133 AGGCCAGAGGATTTGGAAGGCTACCAGAGAGAAGCAGCCGAGGCCTGATTGTGGAAATGATGCTT AGGCCAGAGGATTTGGAAGGCTACCAGAGAGAGGCAGCCGAGGCCTGATTGTGGAAATGATGCTT A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102780127..102780207 26863196 MeRIP-seq:(Medium) rs3803286 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7403,GWAS_ID_7404,GWAS_ID_7405,GWAS_ID_7406,GWAS_ID_7407,GWAS_ID_7408,GWAS_ID_7409,GWAS_ID_7410,GWAS_ID_7411,GWAS_ID_7412,GWAS_ID_7413,GWAS_ID_7414,GWAS_ID_7415,GWAS_ID_7416,GWAS_ID_7417,GWAS_ID_7418,GWAS_ID_7419,GWAS_ID_7420,GWAS_ID_7421,GWAS_ID_7422,GWAS_ID_7423,GWAS_ID_7424,GWAS_ID_7425 RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 61093 RMVar_ID_61093 Human_SNP_ID_567933393 m1A Human chr14 + 102826491 102826490 102826491 TCGGGGGAGCTCAGGGAAAGGGCCTTGCTGCCAGGGGTGGGAAGGGAGTCAGTGAAGACGTCCTG TCGGGGGAGCTCAGGGAAAGGGCCTTGCTGCC_GGGGTGGGAAGGGAGTCAGTGAAGACGTCCTG CA C TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102826487..102826576 26863196 MeRIP-seq:(Medium) rs528113199 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 61094 RMVar_ID_61094 Human_SNP_ID_567946854 m1A Human chr14 - 102878403 102878403 102878403 CCATACACACACACCCACATTCACACACCCCCACACACTCACCCACATTCACACTCACCCCCACA CCATACACACACACCCACATTCACACACCCCCCCACACTCACCCACATTCACACTCACCCCCACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102878402..102878495 26863196 MeRIP-seq:(Medium) rs1171370898 Functional Loss SNV dbSNP153 33..33 33 - - - 61095 RMVar_ID_61095 Human_SNP_ID_567958010 m1A Human chr14 + 102919699 102919696 102919700 ACCTTCCATCCATCTACCATCCATCATCCACCACCCATCTATCCCCATTCACCATCCACCATCAC ACCTTCCATCCATCTACCATCCATCATCCA____CCATCTATCCCCATTCACCATCCACCATCAC ACCAC A lnc-AMN-2 RNACentral:URS00008B95DD lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102919477..102919781 26863196 MeRIP-seq:(Medium) rs1227524425 Functional Loss DEL dbSNP153 31..34 33 - - - 61096 RMVar_ID_61096 Human_SNP_ID_567958167 m1A Human chr14 + 102920243 102920243 102920243 ACCATTCATTTATCCACCGTCCATTCATGCATACATCCACCATCCATCTATCCACCATTCATCCA ACCATTCATTTATCCACCGTCCATTCATGCATGCATCCACCATCCATCTATCCACCATTCATCCA A G lnc-AMN-2 RNACentral:URS00008B95DD lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102920093..102921323 26863196 MeRIP-seq:(Medium) rs1566823222 Functional Loss SNV dbSNP153 33..33 33 - - - 61097 RMVar_ID_61097 Human_SNP_ID_567958168 m1A Human chr14 + 102920243 102920243 102920243 ACCATTCATTTATCCACCGTCCATTCATGCATACATCCACCATCCATCTATCCACCATTCATCCA ACCATTCATTTATCCACCGTCCATTCATGCATTCATCCACCATCCATCTATCCACCATTCATCCA A T lnc-AMN-2 RNACentral:URS00008B95DD lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102920093..102921323 26863196 MeRIP-seq:(Medium) rs1566823222 Functional Loss SNV dbSNP153 33..33 33 - - - 61098 RMVar_ID_61098 Human_SNP_ID_567962802 m1A Human chr14 + 102932651 102932651 102932651 GACCGGTGGGAGGACAGGGGAAGCCTGGCCCAAGCTGTGGACAAGCTGTGTCTGCCGCCACAGTT GACCGGTGGGAGGACAGGGGAAGCCTGGCCCAGGCTGTGGACAAGCTGTGTCTGCCGCCACAGTT A G AMN Ensembl:ENSG00000166126 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102932601..102932777 32194978 MeRIP-seq:(Medium) rs1017572437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3468217 Human_Splice_Rec_1557740,Human_Splice_Rec_1557741 61099 RMVar_ID_61099 Human_SNP_ID_567963026 m1A Human chr14 - 102933111 102933111 102933111 CAGGACCAGTGACACCCTGCGTCCCTGTGTGCATTAAGTTCATTCTGGGTCGCAGCCATGAAGTG CAGGACCAGTGACACCCTGCGTCCCTGTGTGCGTTAAGTTCATTCTGGGTCGCAGCCATGAAGTG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26920484,Human_RBP_ID_27224015 Human_miRNA_ID_359331,Human_miRNA_ID_1475318,Human_miRNA_ID_1480278,Human_miRNA_ID_2888625,Human_miRNA_ID_2888972 GWAS_ID_7426,GWAS_ID_7427,GWAS_ID_7428,GWAS_ID_7429,GWAS_ID_7430,GWAS_ID_7431 RMVar_hsa_circ_110689,RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_93325,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169454,RMVar_hsa_circ_169455,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450 61100 RMVar_ID_61100 Human_SNP_ID_567963027 m1A Human chr14 - 102933111 102933111 102933111 CAGGACCAGTGACACCCTGCGTCCCTGTGTGCATTAAGTTCATTCTGGGTCGCAGCCATGAAGTG CAGGACCAGTGACACCCTGCGTCCCTGTGTGCCTTAAGTTCATTCTGGGTCGCAGCCATGAAGTG T G CDC42BPB Ensembl:ENSG00000198752 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26920484,Human_RBP_ID_27224015 Human_miRNA_ID_359331,Human_miRNA_ID_1475318,Human_miRNA_ID_1480278,Human_miRNA_ID_2888625,Human_miRNA_ID_2888972 GWAS_ID_7426,GWAS_ID_7427,GWAS_ID_7428,GWAS_ID_7429,GWAS_ID_7430,GWAS_ID_7431 RMVar_hsa_circ_110689,RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_93325,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169454,RMVar_hsa_circ_169455,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450 61101 RMVar_ID_61101 Human_SNP_ID_567965288 m1A Human chr14 - 102939727 102939727 102939727 CCATGAATCTCAAAAGTGTGTCCTTTCCCCAGAGAGATGCTTAGAGACCCAGAATTGAGATCCAA CCATGAATCTCAAAAGTGTGTCCTTTCCCCAGGGAGATGCTTAGAGACCCAGAATTGAGATCCAA T C CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102938410..102939750 32194978 MeRIP-seq:(Medium) rs148066338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27808599 Human_Splice_Rec_1557822 RMVar_hsa_circ_110689,RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_93325,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_107326,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169454,RMVar_hsa_circ_169455,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450,RMVar_hsa_circ_295689,RMVar_hsa_circ_169458,RMVar_hsa_circ_46853,RMVar_hsa_circ_79054,RMVar_hsa_circ_16117,RMVar_hsa_circ_169459,RMVar_hsa_circ_169457,RMVar_hsa_circ_112747,RMVar_hsa_circ_94100,RMVar_hsa_circ_111755,RMVar_hsa_circ_169460,RMVar_hsa_circ_104397,RMVar_hsa_circ_169462,RMVar_hsa_circ_169463,RMVar_hsa_circ_169461 61102 RMVar_ID_61102 Human_SNP_ID_567966658 m1A Human chr14 - 102943969 102943969 102943969 AAAGCGAGGAGTACCTGCTTTGCTTCAGCCACATGGGACTGTACGTGGACCCGCAAGGCCGGAGG AAAGCGAGGAGTACCTGCTTTGCTTCAGCCACGTGGGACTGTACGTGGACCCGCAAGGCCGGAGG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102943918..102944168 32194978 MeRIP-seq:(Medium) rs944799076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40450,Human_RBP_ID_5463142,Human_RBP_ID_8792966,Human_RBP_ID_9323901,Human_RBP_ID_22044696,Human_RBP_ID_22183521,Human_RBP_ID_26920527,Human_RBP_ID_27429611 Human_Splice_Rec_1557815 RMVar_hsa_circ_110689,RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_93325,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_107326,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169454,RMVar_hsa_circ_169455,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450,RMVar_hsa_circ_169458,RMVar_hsa_circ_79054,RMVar_hsa_circ_16117,RMVar_hsa_circ_169459,RMVar_hsa_circ_169466,RMVar_hsa_circ_94100,RMVar_hsa_circ_111755,RMVar_hsa_circ_41369,RMVar_hsa_circ_169462,RMVar_hsa_circ_169461,RMVar_hsa_circ_127645,RMVar_hsa_circ_169464,RMVar_hsa_circ_39444,RMVar_hsa_circ_335121,RMVar_hsa_circ_372020,RMVar_hsa_circ_354629,RMVar_hsa_circ_68630,RMVar_hsa_circ_169467 61103 RMVar_ID_61103 Human_SNP_ID_567972625 m1A Human chr14 - 102963083 102963083 102963083 GAAGAAATGGAAATTTTGAAGAAAAAGATGGAAGAAAAATTCAGAGCAGATACTGGTAAATTAAT GAAGAAATGGAAATTTTGAAGAAAAAGATGGAGGAAAAATTCAGAGCAGATACTGGTAAATTAAT T C CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34301396 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_1815004,Human_RBP_ID_3442246,Human_RBP_ID_22921280 Human_Splice_Rec_1557794,Human_Splice_Rec_1557795,Human_Splice_Rec_1557848,Human_Splice_Rec_1557849 Human_miRNA_ID_2908043,Human_miRNA_ID_3026881 GWAS_ID_7432,GWAS_ID_7433,GWAS_ID_7434,GWAS_ID_7435,GWAS_ID_7436,GWAS_ID_7437,GWAS_ID_7438,GWAS_ID_7439,GWAS_ID_7440,GWAS_ID_7441,GWAS_ID_7442,GWAS_ID_7443,GWAS_ID_7444,GWAS_ID_7445,GWAS_ID_7446,GWAS_ID_7447,GWAS_ID_7448,GWAS_ID_7449,GWAS_ID_7450,GWAS_ID_7451,GWAS_ID_7452,GWAS_ID_7453,GWAS_ID_7454,GWAS_ID_7455,GWAS_ID_7456 RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450,RMVar_hsa_circ_16117,RMVar_hsa_circ_50591,RMVar_hsa_circ_111755,RMVar_hsa_circ_41369,RMVar_hsa_circ_169461,RMVar_hsa_circ_127645,RMVar_hsa_circ_169464,RMVar_hsa_circ_39444,RMVar_hsa_circ_68630,RMVar_hsa_circ_169470,RMVar_hsa_circ_91123,RMVar_hsa_circ_342986,RMVar_hsa_circ_323883,RMVar_hsa_circ_266038,RMVar_hsa_circ_301720,RMVar_hsa_circ_53364,RMVar_hsa_circ_169472,RMVar_hsa_circ_6568,RMVar_hsa_circ_289506,RMVar_hsa_circ_169473 61104 RMVar_ID_61104 Human_SNP_ID_567973855 m1A Human chr14 - 102967067 102967067 102967067 CAAGAAGGAGTCAGTGGCCCACTGGGAAGCTCAGATTGCGGAAATCATTCAGTGGTACGTGCGCG CAAGAAGGAGTCAGTGGCCCACTGGGAAGCTCTGATTGCGGAAATCATTCAGTGGTACGTGCGCG T A CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:102967051..102967125 32194978 MeRIP-seq:(Medium) rs1461545624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4282773,Human_RBP_ID_18645699 Human_Splice_Rec_1557789,Human_Splice_Rec_1557843 Human_miRNA_ID_2404210 RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450,RMVar_hsa_circ_16117,RMVar_hsa_circ_50591,RMVar_hsa_circ_111755,RMVar_hsa_circ_41369,RMVar_hsa_circ_169461,RMVar_hsa_circ_127645,RMVar_hsa_circ_169464,RMVar_hsa_circ_39444,RMVar_hsa_circ_68630,RMVar_hsa_circ_169470,RMVar_hsa_circ_91123,RMVar_hsa_circ_323883,RMVar_hsa_circ_266038,RMVar_hsa_circ_53364,RMVar_hsa_circ_332917 61105 RMVar_ID_61105 Human_SNP_ID_567975314 m1A Human chr14 - 102971992 102971990 102971993 GGTGTCCCGGCAGCTGCGAGACAAGGAGGAGGAGATGGAGGTGGCCACGCAGAAGGTGGACGCCA GGTGTCCCGGCAGCTGCGAGACAAGGAGGAG___ATGGAGGTGGCCACGCAGAAGGTGGACGCCA TCTC T CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102971894..102972081 26863196 MeRIP-seq:(Medium) rs772654550 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_813722,Human_RBP_ID_5523100,Human_RBP_ID_8798058,Human_RBP_ID_9282751,Human_RBP_ID_9370492,Human_RBP_ID_18981012,Human_RBP_ID_26325501,Human_RBP_ID_27808607 Human_Splice_Rec_1557781 RMVar_hsa_circ_125390,RMVar_hsa_circ_108427,RMVar_hsa_circ_169451,RMVar_hsa_circ_169450,RMVar_hsa_circ_111755,RMVar_hsa_circ_41369,RMVar_hsa_circ_169461,RMVar_hsa_circ_127645,RMVar_hsa_circ_169464,RMVar_hsa_circ_39444,RMVar_hsa_circ_68630,RMVar_hsa_circ_169470,RMVar_hsa_circ_91123,RMVar_hsa_circ_266038,RMVar_hsa_circ_53364,RMVar_hsa_circ_111131,RMVar_hsa_circ_105821,RMVar_hsa_circ_110907,RMVar_hsa_circ_127800,RMVar_hsa_circ_169475,RMVar_hsa_circ_169476,RMVar_hsa_circ_20839,RMVar_hsa_circ_169478,RMVar_hsa_circ_169479,RMVar_hsa_circ_120295,RMVar_hsa_circ_346493,RMVar_hsa_circ_169481,RMVar_hsa_circ_23842 61106 RMVar_ID_61106 Human_SNP_ID_568000295 m1A Human chr14 - 103058419 103058419 103058419 CATCAGCCTCCCTCCCCCAGCCACCCAAATTAACCAACAATCTTAGTAAATGCAGCGACTCGCTA CATCAGCCTCCCTCCCCCAGCCACCCAAATTACCCAACAATCTTAGTAAATGCAGCGACTCGCTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:103058382..103058737 26863196 MeRIP-seq:(Medium) rs548284589 Functional Loss SNV dbSNP153 33..33 33 - - - 61107 RMVar_ID_61107 Human_SNP_ID_568003525 m1A Human chr14 + 103071678 103071678 103071678 GCCTCTATTGTCATCCTCGTGAGGCTTCACGGAGGTTGCGGGTGCAGCCCGCAGTCACACTGGGG GCCTCTATTGTCATCCTCGTGAGGCTTCACGGTGGTTGCGGGTGCAGCCCGCAGTCACACTGGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103071667..103071740 26863196 MeRIP-seq:(Medium) rs928426471 Functional Loss SNV dbSNP153 33..33 33 - - - 61108 RMVar_ID_61108 Human_SNP_ID_568019096 m1A Human chr14 + 103123888 103123888 103123888 TGCGCCTTCCACATCCTGCCCAGGACTGAAGGAGCCGGGCCCAGCGAGCTCCCGGGAGGTGTGTG TGCGCCTTCCACATCCTGCCCAGGACTGAAGGCGCCGGGCCCAGCGAGCTCCCGGGAGGTGTGTG A C TNFAIP2 Ensembl:ENSG00000185215 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103123837..103123975 26863196 MeRIP-seq:(Medium) rs1368964932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944690,Human_RBP_ID_26325506 Human_Splice_Rec_1557973 61109 RMVar_ID_61109 Human_SNP_ID_568020516 m1A Human chr14 - 103128542 103128542 103128542 TATACCTCCAGGCTTCCTTCCTAAAGTTTCACACTAGGATCTGGGGCCAGCAGTGGCCAAGCCCC TATACCTCCAGGCTTCCTTCCTAAAGTTTCACCCTAGGATCTGGGGCCAGCAGTGGCCAAGCCCC T G lnc-CDC42BPB-4,lnc-CDC42BPB-4:2,lnc-CDC42BPB-4:3 RNACentral:URS0000D58481,RNACentral:URS0000D5D25D,RNACentral:URS0000D56CAA lincRNA,lincRNA,lincRNA intron,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103128539..103128743 26863196 MeRIP-seq:(Medium) rs1234605003 Functional Loss SNV dbSNP153 33..33 33 - - - 61110 RMVar_ID_61110 Human_SNP_ID_568041039 m1A Human chr14 - 103207066 103207066 103207066 CCCAATGACGAGATGCAGATGAACTGAGGAGGAAGAGCGTTTTTATTTTCTGCAACTGGTTACAG CCCAATGACGAGATGCAGATGAACTGAGGAGGGAGAGCGTTTTTATTTTCTGCAACTGGTTACAG T C lnc-CDC42BPB-5,lnc-CDC42BPB-5:2,lnc-CDC42BPB-5:3,lnc-CDC42BPB-5:4,lnc-CDC42BPB-5:5 RNACentral:URS0000D578D9,RNACentral:URS0000D5A36E,RNACentral:URS0000D5DF42,RNACentral:URS0000D5B440,RNACentral:URS0000D5B8BE lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103207015..103207133 26863196 MeRIP-seq:(Medium) rs376063844 Functional Loss SNV dbSNP153 33..33 33 - - - 61111 RMVar_ID_61111 Human_SNP_ID_568075282 m1A Human chr14 - 103334494 103334494 103334494 AACCCGAGTCCGAGTCCGAGGAGGCGGAGGCGAAGCGCAGCGAGGAGCGGCCGGGCCAGGTGCCG AACCCGAGTCCGAGTCCGAGGAGGCGGAGGCGTAGCGCAGCGAGGAGCGGCCGGGCCAGGTGCCG T A LOC105370687-001 RNACentral:URS0000D77FE8 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:103334401..103334600 32194978 MeRIP-seq:(Medium) rs1431835135 Functional Loss SNV dbSNP153 33..33 33 - - - 61112 RMVar_ID_61112 Human_SNP_ID_568091645 m1A Human chr14 + 103385455 103385455 103385455 GAGGCTCTGAGGTGCCGGGGTGCGGCGGCGGCAGCGGCGGCCAGCAGGGCGGAGGCTGAGGCAGC GAGGCTCTGAGGTGCCGGGGTGCGGCGGCGGCGGCGGCGGCCAGCAGGGCGGAGGCTGAGGCAGC A G MARK3 Ensembl:ENSG00000075413 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:103385401..103385897;chr14:103385391..103385900;chr14:103385391..103386299;chr14:103385391..103385975 26863196 MeRIP-seq:(Medium) rs775428569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230894,Human_RBP_ID_812762,Human_RBP_ID_4283085,Human_RBP_ID_18418032 RMVar_hsa_circ_118879,RMVar_hsa_circ_169501 61113 RMVar_ID_61113 Human_SNP_ID_568091757 m1A Human chr14 + 103385788 103385788 103385788 CGCAGCCCGCCGCCCGCAGGCTCGGCTCCGCCACTGCCGCCCTCCCGGTCTCCTCGCCTCGGCCG CGCAGCCCGCCGCCCGCAGGCTCGGCTCCGCCCCTGCCGCCCTCCCGGTCTCCTCGCCTCGGCCG A C MARK3 Ensembl:ENSG00000075413 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:103385550..103385950 26863196 MeRIP-seq:(Medium) rs1262059780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230897,Human_RBP_ID_9324133 RMVar_hsa_circ_118879,RMVar_hsa_circ_169501 61114 RMVar_ID_61114 Human_SNP_ID_568091853 m1A Human chr14 + 103386039 103386039 103386039 GTGCAGAATTAAAGTGCAGTAAAATGTCCACTAGGACCCCATTGCCAACGGTGAATGAACGAGAC GTGCAGAATTAAAGTGCAGTAAAATGTCCACTGGGACCCCATTGCCAACGGTGAATGAACGAGAC A G MARK3 Ensembl:ENSG00000075413 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:103385990..103386299 26863196 MeRIP-seq:(Medium) rs1248724256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38852,Human_RBP_ID_297400,Human_RBP_ID_441748,Human_RBP_ID_1488759,Human_RBP_ID_1815144,Human_RBP_ID_3442412,Human_RBP_ID_8399645,Human_RBP_ID_8793078,Human_RBP_ID_12279485,Human_RBP_ID_18418300,Human_RBP_ID_18645857,Human_RBP_ID_24367298 Human_Splice_Rec_1558243,Human_Splice_Rec_1558277,Human_Splice_Rec_1558313,Human_Splice_Rec_1558317,Human_Splice_Rec_1558349,Human_Splice_Rec_1558379,Human_Splice_Rec_1558409,Human_Splice_Rec_1558441,Human_Splice_Rec_1558453,Human_Splice_Rec_1558467 Human_miRNA_ID_2132640 RMVar_hsa_circ_118879,RMVar_hsa_circ_169501,RMVar_hsa_circ_169502 61115 RMVar_ID_61115 Human_SNP_ID_568096909 m1A Human chr14 - 103405033 103405032 103405034 GCATACACAAAGATAAGGAAATGAGAGAACACAGAGTACTTGCCAAGTTCTAAGAGCTTCTAATT GCATACACAAAGATAAGGAAATGAGAGAACA__GAGTACTTGCCAAGTTCTAAGAGCTTCTAATT CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:103405032..103405145 26863196 MeRIP-seq:(Medium) rs758882943 Functional Loss DEL dbSNP153 32..33 33 - - - 61116 RMVar_ID_61116 Human_SNP_ID_568096914 m1A Human chr14 - 103405042 103405042 103405042 TGCAATACAGCATACACAAAGATAAGGAAATGAGAGAACACAGAGTACTTGCCAAGTTCTAAGAG TGCAATACAGCATACACAAAGATAAGGAAATGGGAGAACACAGAGTACTTGCCAAGTTCTAAGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103405040..103405156 26863196 MeRIP-seq:(Medium) rs768447631 Functional Loss SNV dbSNP153 33..33 33 - - - 61117 RMVar_ID_61117 Human_SNP_ID_568117246 m1A Human chr14 + 103480464 103480464 103480464 TGCAGTGAGAGAACTACAGCTGATAGACACTCAGTGATTCAGAATGGCAAAGAAAACAGGTAGGA TGCAGTGAGAGAACTACAGCTGATAGACACTCGGTGATTCAGAATGGCAAAGAAAACAGGTAGGA A G MARK3 Ensembl:ENSG00000075413 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:103480396..103489403 32194978 MeRIP-seq:(Medium) rs1457220619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1488832,Human_RBP_ID_1815254,Human_RBP_ID_9370525,Human_RBP_ID_12281373,Human_RBP_ID_22921398,Human_RBP_ID_23612866,Human_RBP_ID_25085000,Human_RBP_ID_26808322 Human_Splice_Rec_1558266,Human_Splice_Rec_1558267,Human_Splice_Rec_1558302,Human_Splice_Rec_1558303,Human_Splice_Rec_1558344,Human_Splice_Rec_1558345,Human_Splice_Rec_1558374,Human_Splice_Rec_1558375,Human_Splice_Rec_1558404,Human_Splice_Rec_1558405,Human_Splice_Rec_1558434,Human_Splice_Rec_1558435,Human_Splice_Rec_1558494,Human_Splice_Rec_1558495,Human_Splice_Rec_1558578,Human_Splice_Rec_1558579,Human_Splice_Rec_1558600,Human_Splice_Rec_1558601,Human_Splice_Rec_1558604,Human_Splice_Rec_1558605,Human_Splice_Rec_1558608,Human_Splice_Rec_1558609 RMVar_hsa_circ_169510,RMVar_hsa_circ_312730,RMVar_hsa_circ_169509,RMVar_hsa_circ_311738,RMVar_hsa_circ_323142,RMVar_hsa_circ_169516,RMVar_hsa_circ_169517,RMVar_hsa_circ_319704,RMVar_hsa_circ_95136,RMVar_hsa_circ_329672,RMVar_hsa_circ_169519,RMVar_hsa_circ_169518,RMVar_hsa_circ_169529,RMVar_hsa_circ_371310,RMVar_hsa_circ_46555,RMVar_hsa_circ_169530,RMVar_hsa_circ_274321,RMVar_hsa_circ_169534,RMVar_hsa_circ_169535,RMVar_hsa_circ_347898,RMVar_hsa_circ_325968,RMVar_hsa_circ_298998,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_290090,RMVar_hsa_circ_307718,RMVar_hsa_circ_169541 61118 RMVar_ID_61118 Human_SNP_ID_568128153 m1A Human chr14 + 103519928 103519928 103519928 CCTGGCCCTGCTCCAGCCGCTGCTCCATCTCGATGAGCAGCTTCACTCCGTCCACCACCATCTGC CCTGGCCCTGCTCCAGCCGCTGCTCCATCTCGGTGAGCAGCTTCACTCCGTCCACCACCATCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103519721..103520001 26863196 MeRIP-seq:(Medium) rs145462676 Functional Loss SNV dbSNP153 33..33 33 - - - 61119 RMVar_ID_61119 Human_SNP_ID_568129049 m1A Human chr14 - 103522081 103522081 103522081 GGATCTCTTCGACCCCATCATCGAGGACCGGCACGGCGGCTACAAGCCCAGCGATGAGCACAAGA GGATCTCTTCGACCCCATCATCGAGGACCGGCGCGGCGGCTACAAGCCCAGCGATGAGCACAAGA T C CKB Ensembl:ENSG00000166165 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr14:103521751..103522528;chr14:103521851..103522525 26863196 MeRIP-seq:(Medium) rs1213631569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231289,Human_RBP_ID_441838,Human_RBP_ID_813155,Human_RBP_ID_997624,Human_RBP_ID_1488974,Human_RBP_ID_1815374,Human_RBP_ID_3442702,Human_RBP_ID_4283227,Human_RBP_ID_5562985,Human_RBP_ID_6327758,Human_RBP_ID_8250011,Human_RBP_ID_8399865,Human_RBP_ID_8793127,Human_RBP_ID_17246623,Human_RBP_ID_17845194,Human_RBP_ID_18469465,Human_RBP_ID_18528758,Human_RBP_ID_18646057,Human_RBP_ID_22921469,Human_RBP_ID_27224155 Human_Splice_Rec_1558630,Human_Splice_Rec_1558631,Human_Splice_Rec_1558658,Human_Splice_Rec_1558659,Human_Splice_Rec_1558686,Human_Splice_Rec_1558690,Human_Splice_Rec_1558691,Human_Splice_Rec_1558695,Human_Splice_Rec_1558702,Human_Splice_Rec_1558703,Human_Splice_Rec_1558708,Human_Splice_Rec_1558711,Human_Splice_Rec_1558716,Human_Splice_Rec_1558717,Human_Splice_Rec_1558720 Human_miRNA_ID_2554407,Human_miRNA_ID_3010744 RMVar_hsa_circ_126066,RMVar_hsa_circ_169546 61120 RMVar_ID_61120 Human_SNP_ID_568129380 m1A Human chr14 + 103522760 103522760 103522760 CCCGGGCGCGGACGCCCCCGGCCCCCGGGCCCACTCACCGGGCGGCCGGGCGGGGGCGGGGGCGC CCCGGGCGCGGACGCCCCCGGCCCCCGGGCCCTCTCACCGGGCGGCCGGGCGGGGGCGGGGGCGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr14:103522751..103522825;chr14:103522751..103522850 26863196 MeRIP-seq:(Medium) rs1312054450 Functional Loss SNV dbSNP153 33..33 33 - - - 61121 RMVar_ID_61121 Human_SNP_ID_568129417 m1A Human chr14 + 103522815 103522815 103522815 GCGGGGGCGCTCCGTCCGTCGGCAGCTCCCGGAGCGACGCAGGCGAACAGCGGCCGCTCCGCGCT GCGGGGGCGCTCCGTCCGTCGGCAGCTCCCGGCGCGACGCAGGCGAACAGCGGCCGCTCCGCGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103522713..103522850 26863196 MeRIP-seq:(Medium) rs1196285268 Functional Loss SNV dbSNP153 33..33 33 - - - 61122 RMVar_ID_61122 Human_SNP_ID_568130942 m1A Human chr14 + 103528959 103528959 103528959 CCTCCCGCCTCGGCCTCCCAAAGCGCGGGATCACAGGCGAGAGCCACCGCGCCGGCCGGCCGCCA CCTCCCGCCTCGGCCTCCCAAAGCGCGGGATCGCAGGCGAGAGCCACCGCGCCGGCCGGCCGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103528925..103529043 26863196 MeRIP-seq:(Medium) rs1441769174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17845202 61123 RMVar_ID_61123 Human_SNP_ID_568131075 m1A Human chr14 + 103529252 103529252 103529252 CGCGGAGGCACGTGTGGAGCCCCGGCAGCAGGAGCGTCGCAGGTGAGACTCCGCGGGGTACAGGG CGCGGAGGCACGTGTGGAGCCCCGGCAGCAGGGGCGTCGCAGGTGAGACTCCGCGGGGTACAGGG A G TRMT61A Ensembl:ENSG00000166166 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103529204..103529312 26863196 MeRIP-seq:(Medium) rs949301971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308536 Human_Splice_Rec_1558721,Human_Splice_Rec_1558727 RMVar_hsa_circ_77093,RMVar_hsa_circ_169550 61124 RMVar_ID_61124 Human_SNP_ID_568131082 m1A Human chr14 + 103529260 103529260 103529260 CACGTGTGGAGCCCCGGCAGCAGGAGCGTCGCAGGTGAGACTCCGCGGGGTACAGGGTGGCAGGG CACGTGTGGAGCCCCGGCAGCAGGAGCGTCGCTGGTGAGACTCCGCGGGGTACAGGGTGGCAGGG A T TRMT61A Ensembl:ENSG00000166166 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:103529233..103529308;chr14:103529236..103529332;chr14:103529211..103529323 26863196 MeRIP-seq:(Medium) rs1338659677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308536 Human_Splice_Rec_1558721,Human_Splice_Rec_1558727 RMVar_hsa_circ_77093,RMVar_hsa_circ_169550 61125 RMVar_ID_61125 Human_SNP_ID_568141005 m1A Human chr14 - 103563082 103563082 103563082 GCCGTATCCCTGCGCTCGGCGCCGCGCTCCGGAGCGAGTTGACAGCCGCGGCAGGCGAAGGCGCG GCCGTATCCCTGCGCTCGGCGCCGCGCTCCGGGGCGAGTTGACAGCCGCGGCAGGCGAAGGCGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103563032..103563118 26863196 MeRIP-seq:(Medium) rs1268847789 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 61126 RMVar_ID_61126 Human_SNP_ID_568159103 m1A Human chr14 - 103629272 103629272 103629272 CCGCCGAGCACAGCCCCGCGGCTCCTCGCACCAGCAGCCCAGCCGACCCAGCCAGTCCCGCTCGG CCGCCGAGCACAGCCCCGCGGCTCCTCGCACCTGCAGCCCAGCCGACCCAGCCAGTCCCGCTCGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:103629176..103629500;chr14:103629201..103629569 26863196 MeRIP-seq:(Medium) rs1014982342 Functional Loss SNV dbSNP153 33..33 33 - - - 61127 RMVar_ID_61127 Human_SNP_ID_568160670 m1A Human chr14 + 103634458 103634458 103634458 CATGTTAAATCTGAAGTGCTTGTGGGGCAGCCAAGTGGACTAGTGGGCAGTTAGAGATACATCTT CATGTTAAATCTGAAGTGCTTGTGGGGCAGCCGAGTGGACTAGTGGGCAGTTAGAGATACATCTT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:103634454..103634596 26863196 MeRIP-seq:(Medium) rs1277649979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6328023,Human_RBP_ID_12283076 RMVar_hsa_circ_124329,RMVar_hsa_circ_169560,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264 61128 RMVar_ID_61128 Human_SNP_ID_568166310 m1A Human chr14 - 103654580 103654580 103654580 CAACTTGTCTTCCTTTATGTACACCATTGTGGACATGTTGTCATACATTCTGGAATGAAAAAAGA CAACTTGTCTTCCTTTATGTACACCATTGTGGGCATGTTGTCATACATTCTGGAATGAAAAAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:103654551..103654675;chr14:103654551..103654625;chr14:103654551..103654650 26863196 MeRIP-seq:(Medium) rs754353645 Functional Loss SNV dbSNP153 33..33 33 - - - 61129 RMVar_ID_61129 Human_SNP_ID_568173163 m1A Human chr14 + 103679471 103679471 103679471 ACATGGAGAAGCGCAGGAGCCGTGAGAGCCTCAACGTGGACGTGGTCAAGTACGAGAGTGGCCCT ACATGGAGAAGCGCAGGAGCCGTGAGAGCCTCGACGTGGACGTGGTCAAGTACGAGAGTGGCCCT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103679422..103679558 26863196 MeRIP-seq:(Medium) rs183764708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39620,Human_RBP_ID_3945153,Human_RBP_ID_6328144,Human_RBP_ID_9039677,Human_RBP_ID_9369567,Human_RBP_ID_12283655,Human_RBP_ID_22926246,Human_RBP_ID_23613202,Human_RBP_ID_26325538,Human_RBP_ID_27808636 Human_Splice_Rec_1558764,Human_Splice_Rec_1558765,Human_Splice_Rec_1558791,Human_Splice_Rec_1558816,Human_Splice_Rec_1558817,Human_Splice_Rec_1558842,Human_Splice_Rec_1558843,Human_Splice_Rec_1558866,Human_Splice_Rec_1558867,Human_Splice_Rec_1558890,Human_Splice_Rec_1558891,Human_Splice_Rec_1558918,Human_Splice_Rec_1558919,Human_Splice_Rec_1558948,Human_Splice_Rec_1558949,Human_Splice_Rec_1558978,Human_Splice_Rec_1558979,Human_Splice_Rec_1559006,Human_Splice_Rec_1559030,Human_Splice_Rec_1559031,Human_Splice_Rec_1559060,Human_Splice_Rec_1559061,Human_Splice_Rec_1559086,Human_Splice_Rec_1559087,Human_Splice_Rec_1559114,Human_Splice_Rec_1559115,Human_Splice_Rec_1559144,Human_Splice_Rec_1559145,Human_Splice_Rec_1559157,Human_Splice_Rec_1559168,Human_Splice_Rec_1559169,Human_Splice_Rec_1559178,Human_Splice_Rec_1559185,Human_Splice_Rec_1559189,Human_Splice_Rec_1559336,Human_Splice_Rec_1559337 RMVar_hsa_circ_102941,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_370173,RMVar_hsa_circ_169566,RMVar_hsa_circ_108065,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_169573,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,RMVar_hsa_circ_169574,RMVar_hsa_circ_169569,RMVar_hsa_circ_169571,RMVar_hsa_circ_169572,RMVar_hsa_circ_169570,RMVar_hsa_circ_169567,RMVar_hsa_circ_169568,RMVar_hsa_circ_343063,RMVar_hsa_circ_369006,RMVar_hsa_circ_23448,RMVar_hsa_circ_169586,RMVar_hsa_circ_169585,RMVar_hsa_circ_338509,RMVar_hsa_circ_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_355040,RMVar_hsa_circ_303713,RMVar_hsa_circ_116514,RMVar_hsa_circ_169591,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 61130 RMVar_ID_61130 Human_SNP_ID_568173177 m1A Human chr14 + 103679493 103679493 103679493 TGAGAGCCTCAACGTGGACGTGGTCAAGTACGAGAGTGGCCCTGACGGAGGGGAGGAAGTGAGTA TGAGAGCCTCAACGTGGACGTGGTCAAGTACGGGAGTGGCCCTGACGGAGGGGAGGAAGTGAGTA A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103679442..103679578 26863196 MeRIP-seq:(Medium) rs1205240454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39620,Human_RBP_ID_3945153,Human_RBP_ID_5112776,Human_RBP_ID_6328147,Human_RBP_ID_9039677,Human_RBP_ID_9369567,Human_RBP_ID_12283659,Human_RBP_ID_22355062,Human_RBP_ID_22926246,Human_RBP_ID_23613202,Human_RBP_ID_26325538,Human_RBP_ID_27808636 Human_Splice_Rec_1558765,Human_Splice_Rec_1558791,Human_Splice_Rec_1558817,Human_Splice_Rec_1558843,Human_Splice_Rec_1558867,Human_Splice_Rec_1558891,Human_Splice_Rec_1558919,Human_Splice_Rec_1558949,Human_Splice_Rec_1558979,Human_Splice_Rec_1559031,Human_Splice_Rec_1559061,Human_Splice_Rec_1559087,Human_Splice_Rec_1559115,Human_Splice_Rec_1559145,Human_Splice_Rec_1559157,Human_Splice_Rec_1559169,Human_Splice_Rec_1559185,Human_Splice_Rec_1559189,Human_Splice_Rec_1559337 Human_miRNA_ID_2353898,Human_miRNA_ID_2353899,Human_miRNA_ID_2573987,Human_miRNA_ID_2573988 RMVar_hsa_circ_102941,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_370173,RMVar_hsa_circ_169566,RMVar_hsa_circ_108065,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_169573,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,RMVar_hsa_circ_169574,RMVar_hsa_circ_169569,RMVar_hsa_circ_169571,RMVar_hsa_circ_169572,RMVar_hsa_circ_169570,RMVar_hsa_circ_169567,RMVar_hsa_circ_169568,RMVar_hsa_circ_343063,RMVar_hsa_circ_369006,RMVar_hsa_circ_23448,RMVar_hsa_circ_169586,RMVar_hsa_circ_169585,RMVar_hsa_circ_338509,RMVar_hsa_circ_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_355040,RMVar_hsa_circ_303713,RMVar_hsa_circ_116514,RMVar_hsa_circ_169591,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 61131 RMVar_ID_61131 Human_SNP_ID_568178001 m1A Human chr14 + 103696879 103696879 103696879 CCAGGGCGTGGTGCCTCCCTAAGGGGATGGTCAGTGTTCTGGGACTGACTGCCAGGCCAGCCCGT CCAGGGCGTGGTGCCTCCCTAAGGGGATGGTCGGTGTTCTGGGACTGACTGCCAGGCCAGCCCGT A G AL049840.6,KLC1 Ensembl:ENSG00000269958,Ensembl:ENSG00000126214 lincRNA,Protein coding exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:103696876..103696972 32194978 MeRIP-seq:(Medium) rs543401111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17118002 RMVar_hsa_circ_103318,RMVar_hsa_circ_84202,RMVar_hsa_circ_169567,RMVar_hsa_circ_169568,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_169593,RMVar_hsa_circ_92719 61132 RMVar_ID_61132 Human_SNP_ID_568180095 m1A Human chr14 + 103703228 103703228 103703228 AGATCTGGCTGCCAAATCGGAGCTTCTGAAGCAGCTCTCCTGGAACGTCAGTGCGCAGCCGCGGC AGATCTGGCTGCCAAATCGGAGCTTCTGAAGCGGCTCTCCTGGAACGTCAGTGCGCAGCCGCGGC A G KLC1 Ensembl:ENSG00000126214 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:103703177..103703377 32194978 MeRIP-seq:(Medium) rs754035692 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3442890 RMVar_hsa_circ_169599 61133 RMVar_ID_61133 Human_SNP_ID_568183877 m1A Human chr14 - 103715329 103715329 103715329 TCGTGGGCGGCAGCGGGCGTGAGGGGTGAGGCAGGGTCAAGGGGCGGGGGCGGCCGCGGGTCTCC TCGTGGGCGGCAGCGGGCGTGAGGGGTGAGGCGGGGTCAAGGGGCGGGGGCGGCCGCGGGTCTCC T C XRCC3 Ensembl:ENSG00000126215 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:103715319..103715404 26863410 MeRIP-seq:(Medium) rs1289457850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260687,Human_RBP_ID_4283782,Human_RBP_ID_8078338,Human_RBP_ID_9323917,Human_RBP_ID_9417847,Human_RBP_ID_26778155 61134 RMVar_ID_61134 Human_SNP_ID_568183922 m1A Human chr14 - 103715410 103715410 103715410 AGTGCGGAACCCGCGGGAGGTGAGGCCCGCCGAGCCGGGCTGCGAGCCGGGCTGCGAGCCGGGCG AGTGCGGAACCCGCGGGAGGTGAGGCCCGCCGCGCCGGGCTGCGAGCCGGGCTGCGAGCCGGGCG T G XRCC3 Ensembl:ENSG00000126215 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:103715025..103715475;chr14:103714969..103715475;chr14:103714985..103715475;chr14:103714983..103715475 26863196 MeRIP-seq:(Medium) rs1258117113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418197 61135 RMVar_ID_61135 Human_SNP_ID_568184144 m1A Human chr14 + 103715852 103715852 103715852 GCCGAGAGGCTGAGGCGGCGTCATGTCCTCCGAGGTGTCCGCGCGCCGCGACGCCAAGAAGCTGG GCCGAGAGGCTGAGGCGGCGTCATGTCCTCCGCGGTGTCCGCGCGCCGCGACGCCAAGAAGCTGG A C ZFYVE21 Ensembl:ENSG00000100711 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:103715779..103715930;chr14:103715813..103715917 26863196 MeRIP-seq:(Medium) rs1273979058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442006,Human_RBP_ID_4283800,Human_RBP_ID_18418198 61136 RMVar_ID_61136 Human_SNP_ID_568184157 m1A Human chr14 - 103715885 103715885 103715885 CGGGCACCATGCGCAGGCCGCTCGGGGAGCGCACCAGCTTCTTGGCGTCGCGGCGCGCGGACACC CGGGCACCATGCGCAGGCCGCTCGGGGAGCGCGCCAGCTTCTTGGCGTCGCGGCGCGCGGACACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103715847..103715933 26863196 MeRIP-seq:(Medium) rs1378546505 Functional Loss SNV dbSNP153 33..33 33 - - - 61137 RMVar_ID_61137 Human_SNP_ID_568189827 m1A Human chr14 + 103734266 103734266 103734266 CCCCTCCTGACACCAGGCGTCTGCCATCCTTCAGGCACCAAACAGCCCCGTCTACCTGGCCCTGG CCCCTCCTGACACCAGGCGTCTGCCATCCTTCCGGCACCAAACAGCCCCGTCTACCTGGCCCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103734218..103734304 26863196 MeRIP-seq:(Medium) rs1265395293 Functional Loss SNV dbSNP153 33..33 33 - - - 61138 RMVar_ID_61138 Human_SNP_ID_568189828 m1A Human chr14 + 103734266 103734266 103734266 CCCCTCCTGACACCAGGCGTCTGCCATCCTTCAGGCACCAAACAGCCCCGTCTACCTGGCCCTGG CCCCTCCTGACACCAGGCGTCTGCCATCCTTCGGGCACCAAACAGCCCCGTCTACCTGGCCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103734218..103734304 26863196 MeRIP-seq:(Medium) rs1265395293 Functional Loss SNV dbSNP153 33..33 33 - - - 61139 RMVar_ID_61139 Human_SNP_ID_568191625 m1A Human chr14 - 103740016 103740016 103740016 GATGCCAATGATAATGAGTTACCTTCCCCCGAACCAGAGGAGCTCATCTGTCCCCAAACCACCCA GATGCCAATGATAATGAGTTACCTTCCCCCGAGCCAGAGGAGCTCATCTGTCCCCAAACCACCCA T C PPP1R13B Ensembl:ENSG00000088808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103739876..103740149 26863196 MeRIP-seq:(Medium) rs1395704616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1559716 Human_miRNA_ID_2894447 RMVar_hsa_circ_90701,RMVar_hsa_circ_169602,RMVar_hsa_circ_121924,RMVar_hsa_circ_267419,RMVar_hsa_circ_265979,RMVar_hsa_circ_56204,RMVar_hsa_circ_169604,RMVar_hsa_circ_266304 61140 RMVar_ID_61140 Human_SNP_ID_568191635 m1A Human chr14 + 103740037 103740037 103740037 AGCTCCTCTGGTTCGGGGGAAGGTAACTCATTATCATTGGCATCTGATGACGGGGCAGGCTCAGC AGCTCCTCTGGTTCGGGGGAAGGTAACTCATTGTCATTGGCATCTGATGACGGGGCAGGCTCAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:103739901..103740118 26863196 MeRIP-seq:(Medium) rs1226245415 Functional Loss SNV dbSNP153 33..33 33 - - - 61141 RMVar_ID_61141 Human_SNP_ID_568191790 m1A Human chr14 + 103740428 103740428 103740428 TGGTGGGGCTGAGTGGCCGTGGCAGGCTCTCCACGGTGCTGCCATCTGCGGGGGCGGCGGGGCCA TGGTGGGGCTGAGTGGCCGTGGCAGGCTCTCCGCGGTGCTGCCATCTGCGGGGGCGGCGGGGCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103740380..103740472 26863196 MeRIP-seq:(Medium) rs1213948733 Functional Loss SNV dbSNP153 33..33 33 - - - 61142 RMVar_ID_61142 Human_SNP_ID_568197036 m1A Human chr14 + 103760765 103760765 103760765 CACGGCAACATCACTTGTTTTCCACAATAAACACGGCCCACCCCGCCTCAGGTCTAGCTAGCCTC CACGGCAACATCACTTGTTTTCCACAATAAACGCGGCCCACCCCGCCTCAGGTCTAGCTAGCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:103760652..103760809 26863196 MeRIP-seq:(Medium) rs968810484 Functional Loss SNV dbSNP153 33..33 33 - - - 61143 RMVar_ID_61143 Human_SNP_ID_568208315 m1A Human chr14 - 103803773 103803773 103803773 GGCAGAGAAGCAGTTTGAGGAAAGGCATAAGTAGGGCATCTTGTCATTACATGCTATATTTGTTA GGCAGAGAAGCAGTTTGAGGAAAGGCATAAGTGGGGCATCTTGTCATTACATGCTATATTTGTTA T C PPP1R13B Ensembl:ENSG00000088808 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103803771..103803929 26863196 MeRIP-seq:(Medium) rs1343211699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8400205,Human_RBP_ID_12285294 61144 RMVar_ID_61144 Human_SNP_ID_568219725 m1A Human chr14 + 103847514 103847514 103847514 GGCCGCCGGCGCGCTGCGTCGCTGTCCCGGGCACCCGGCCGCCGCCGCCGCCGCCTCAACCTCAG GGCCGCCGGCGCGCTGCGTCGCTGTCCCGGGCCCCCGGCCGCCGCCGCCGCCGCCTCAACCTCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:103847321..103847570 26863196 MeRIP-seq:(Medium) rs953041051 Functional Loss SNV dbSNP153 33..33 33 - - - 61145 RMVar_ID_61145 Human_SNP_ID_568238344 m1A Human chr14 + 103915176 103915176 103915176 AGGGCTTCATGGGGATCCATATGTTTTTAATAATACTTTGAAGCATCTGAAAATGAACACAGTGA AGGGCTTCATGGGGATCCATATGTTTTTAATAGTACTTTGAAGCATCTGAAAATGAACACAGTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:103915126..103915202 26863196 MeRIP-seq:(Medium) rs368692211 Functional Loss SNV dbSNP153 33..33 33 - - - 61146 RMVar_ID_61146 Human_SNP_ID_568238505 m1A Human chr14 - 103915788 103915788 103915788 GAGTTGGAAGAGCTGTGGAAAGCATGAGTCCCAGGCCGGGCCCTGTGGCTCACACCGTAATCCTA GAGTTGGAAGAGCTGTGGAAAGCATGAGTCCCGGGCCGGGCCCTGTGGCTCACACCGTAATCCTA T C ATP5MPL Ensembl:ENSG00000156411 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:103915779..103915912 26863196 MeRIP-seq:(Medium) rs1474369175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81085,RMVar_hsa_circ_169620 61147 RMVar_ID_61147 Human_SNP_ID_568240187 m1A Human chr14 + 103921454 103921454 103921454 CCCCGCCGTCTCGCACCTCGGGAGCCAGGTCCAGGTCCCCGTACTCACCTTGGCGCAGGACAGAC CCCCGCCGTCTCGCACCTCGGGAGCCAGGTCCTGGTCCCCGTACTCACCTTGGCGCAGGACAGAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:103921451..103921525 26863196 MeRIP-seq:(Medium) rs528650673 Functional Loss SNV dbSNP153 33..33 33 - - - 61148 RMVar_ID_61148 Human_SNP_ID_568296706 m1A Human chr14 + 104137920 104137920 104137920 GCCTGCTGACAACAGGTCCGGCGCACGCCCGCAGGACCTCCCGCTTCCCGGGCGGCACGGCGCGC GCCTGCTGACAACAGGTCCGGCGCACGCCCGCGGGACCTCCCGCTTCCCGGGCGGCACGGCGCGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104137870..104137993 32194978 MeRIP-seq:(Medium) rs1293833796 Functional Loss SNV dbSNP153 33..33 33 - - - 61149 RMVar_ID_61149 Human_SNP_ID_568300974 m1A Human chr14 + 104152144 104152144 104152144 CCACACACCTGCAGCAGCTCACACGGGAGGCCATGCACCTGCTGCAGGCCCCTGCCAGCCATGAG CCACACACCTGCAGCAGCTCACACGGGAGGCCGTGCACCTGCTGCAGGCCCCTGCCAGCCATGAG A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104152093..104152480 26863196 MeRIP-seq:(Medium) rs758189946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18646438,Human_RBP_ID_27429817 RMVar_hsa_circ_318351 61150 RMVar_ID_61150 Human_SNP_ID_568300984 m1A Human chr14 + 104152175 104152175 104152175 CATGCACCTGCTGCAGGCCCCTGCCAGCCATGAGGACCTTGACGCCCCCCATGGAGGCCCCAGCC CATGCACCTGCTGCAGGCCCCTGCCAGCCATGGGGACCTTGACGCCCCCCATGGAGGCCCCAGCC A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:104152151..104152175 26863196 MeRIP-seq:(Medium) rs749757071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18646438 RMVar_hsa_circ_318351 61151 RMVar_ID_61151 Human_SNP_ID_568301413 m1A Human chr14 + 104153448 104153448 104153448 TGAGGCCGAGGAGAGGGAGCCCCACCCTTGCCACGAGGTGCCTCCTGGCCCCAGAGCTGAACCCC TGAGGCCGAGGAGAGGGAGCCCCACCCTTGCCCCGAGGTGCCTCCTGGCCCCAGAGCTGAACCCC A C KIF26A Ensembl:ENSG00000066735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104153444..104153606 26863196 MeRIP-seq:(Medium) rs1410936786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318351 61152 RMVar_ID_61152 Human_SNP_ID_568301448 m1A Human chr14 + 104153560 104153536 104153560 TGCCATGAGGTGCCTCCTGGCCCCAGAGCCGAACCCCACCCTTGCCACGAGGTGCCTCCTGGCCC TGCCATGAG________________________CCCCACCCTTGCCACGAGGTGCCTCCTGGCCC GGTGCCTCCTGGCCCCAGAGCCGAA G KIF26A Ensembl:ENSG00000066735 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr14:104153452..104153606;chr14:104153434..104153560 26863196 MeRIP-seq:(Medium) rs1160809844 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_27429818 RMVar_hsa_circ_318351 61153 RMVar_ID_61153 Human_SNP_ID_568309408 m1A Human chr14 - 104175518 104175518 104175518 CCCCAGACAATGGCCTTGCAGGGCTCAGGGGTACCCTGGTGGGTGTCTGGACCAGAACTGCCTCG CCCCAGACAATGGCCTTGCAGGGCTCAGGGGTGCCCTGGTGGGTGTCTGGACCAGAACTGCCTCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104175268..104175667 32194978 MeRIP-seq:(Medium) rs1340469203 Functional Loss SNV dbSNP153 33..33 33 - - - 61154 RMVar_ID_61154 Human_SNP_ID_568309441 m1A Human chr14 + 104175598 104175598 104175598 CAGCAGCGCTTGGCCTGAGCTGCTGGTCCCGGAAAAGGCTGCAGTGAGTGGAGGCAGGAGGCCAC CAGCAGCGCTTGGCCTGAGCTGCTGGTCCCGGGAAAGGCTGCAGTGAGTGGAGGCAGGAGGCCAC A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104175547..104175728 26863196 MeRIP-seq:(Medium) rs74324704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61155 RMVar_ID_61155 Human_SNP_ID_568309635 m1A Human chr14 - 104175996 104175975 104175996 ATTGATGCTGCTGATGATGCTGACTGGCCGGGACCCCGAGGCCAGGGCCCGCAGGGAGCAGTCAC ATTGATGCTGCTGATGATGCTGACTGGCCGGG_____________________GGGAGCAGTCAC CTGCGGGCCCTGGCCTCGGGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104175950..104176058 26863196 MeRIP-seq:(Medium) rs1566865590 Functional Loss DEL dbSNP153 33..53 33 - - - 61156 RMVar_ID_61156 Human_SNP_ID_568309649 m1A Human chr14 - 104175996 104175996 104175996 ATTGATGCTGCTGATGATGCTGACTGGCCGGGACCCCGAGGCCAGGGCCCGCAGGGAGCAGTCAC ATTGATGCTGCTGATGATGCTGACTGGCCGGGGCCCCGAGGCCAGGGCCCGCAGGGAGCAGTCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104175950..104176058 26863196 MeRIP-seq:(Medium) rs1300888262 Functional Loss SNV dbSNP153 33..33 33 - - - 61157 RMVar_ID_61157 Human_SNP_ID_568309862 m1A Human chr14 - 104176319 104176319 104176319 GGTCGGGATGGGGCCACTGCAGCCACTTCCCCAGGGCACGGACCCCAGGTTGGCCCAGGACTGTC GGTCGGGATGGGGCCACTGCAGCCACTTCCCCGGGGCACGGACCCCAGGTTGGCCCAGGACTGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104176268..104176373 26863196 MeRIP-seq:(Medium) rs758328099 Functional Loss SNV dbSNP153 33..33 33 - - - 61158 RMVar_ID_61158 Human_SNP_ID_568309979 m1A Human chr14 + 104176563 104176563 104176563 GGGAGTGTGATACCCAGGCAGCTTCTGCTGGCAGGGCCCCCAGCCCCACACTTGGCTCCCCCCGG GGGAGTGTGATACCCAGGCAGCTTCTGCTGGCCGGGCCCCCAGCCCCACACTTGGCTCCCCCCGG A C KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104176513..104176720 26863196 MeRIP-seq:(Medium) rs1423715695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61159 RMVar_ID_61159 Human_SNP_ID_568309980 m1A Human chr14 + 104176563 104176563 104176563 GGGAGTGTGATACCCAGGCAGCTTCTGCTGGCAGGGCCCCCAGCCCCACACTTGGCTCCCCCCGG GGGAGTGTGATACCCAGGCAGCTTCTGCTGGCGGGGCCCCCAGCCCCACACTTGGCTCCCCCCGG A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104176513..104176720 26863196 MeRIP-seq:(Medium) rs1423715695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61160 RMVar_ID_61160 Human_SNP_ID_568310041 m1A Human chr14 + 104176700 104176700 104176700 GCCCGCAGGCCAGAGGCTGTGGCTCGGATCCCACCGCTGCGGAGGGGTGCCACCACGCTGGGTGT GCCCGCAGGCCAGAGGCTGTGGCTCGGATCCCGCCGCTGCGGAGGGGTGCCACCACGCTGGGTGT A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:104176676..104176700 26863196 MeRIP-seq:(Medium) rs1188704406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61161 RMVar_ID_61161 Human_SNP_ID_568310099 m1A Human chr14 - 104176803 104176803 104176803 CTTGGGAGCCAGACCCTTCTTGCTGGTGGGGGAGGCCTTCAGGCTCCCCGAGCAGGCCACCACCT CTTGGGAGCCAGACCCTTCTTGCTGGTGGGGGGGGCCTTCAGGCTCCCCGAGCAGGCCACCACCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:104176697..104176850 26863196 MeRIP-seq:(Medium) rs868030595 Functional Loss SNV dbSNP153 33..33 33 - - - 61162 RMVar_ID_61162 Human_SNP_ID_568310236 m1A Human chr14 + 104177046 104177035 104177047 ACCACTCTGTCCCCAGGGCCACGTCCAGCCTGAAGGCCCGGGCCAGCAAGGTAGAAGCAGCACAC ACCACTCTGTCCCCAGGGCCAC____________GGCCCGGGCCAGCAAGGTAGAAGCAGCACAC CGTCCAGCCTGAA C KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104177002..104177122 26863196 MeRIP-seq:(Medium) rs1566866413 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61163 RMVar_ID_61163 Human_SNP_ID_568310241 m1A Human chr14 + 104177046 104177046 104177046 ACCACTCTGTCCCCAGGGCCACGTCCAGCCTGAAGGCCCGGGCCAGCAAGGTAGAAGCAGCACAC ACCACTCTGTCCCCAGGGCCACGTCCAGCCTGGAGGCCCGGGCCAGCAAGGTAGAAGCAGCACAC A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104177002..104177122 26863196 MeRIP-seq:(Medium) rs1462392899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633 61164 RMVar_ID_61164 Human_SNP_ID_568311396 m1A Human chr14 - 104179249 104179249 104179249 GCCTGCGCTCCGCCAGCCGCAGCCTTGTACTGACGCACGCCAGACCCTGGGAGGCAGGGCGGGCG GCCTGCGCTCCGCCAGCCGCAGCCTTGTACTGGCGCACGCCAGACCCTGGGAGGCAGGGCGGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104178552..104179281 26863196 MeRIP-seq:(Medium) rs1032583938 Functional Loss SNV dbSNP153 33..33 33 - - - 61165 RMVar_ID_61165 Human_SNP_ID_568312028 m1A Human chr14 + 104180566 104180566 104180566 TAGGTTCATATTTTTATATCATTTTGCCCATAAATGCGGAATTTGCCGTGGGAATTTGAAGACAA TAGGTTCATATTTTTATATCATTTTGCCCATACATGCGGAATTTGCCGTGGGAATTTGAAGACAA A C KIF26A Ensembl:ENSG00000066735 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104180516..104180589 26863196 MeRIP-seq:(Medium) rs1313907664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442078,Human_RBP_ID_8400322 RMVar_hsa_circ_90113,RMVar_hsa_circ_116512,RMVar_hsa_circ_92280,RMVar_hsa_circ_169631,RMVar_hsa_circ_124849,RMVar_hsa_circ_169632,RMVar_hsa_circ_169633,RMVar_hsa_circ_120652,RMVar_hsa_circ_169634,RMVar_hsa_circ_169635 61166 RMVar_ID_61166 Human_SNP_ID_568320654 m1A Human chr14 + 104209087 104208986 104209088 ACCAGCAGAGCTGGGACACCACCAGAGCTGTGAGACCACCAGAGCCGGGACACCACCAGAGCCGG __________________________________ACCACCAGAGCCGGGACACCACCAGAGCCGG CACCACCAGAGCTGGGACACCACCAGAGCTGCGAGACCACCAGAGCCGTGACACCACCAGAGCCGTGACACCAGCAGAGCTGGGACACCACCAGAGCTGTGAG C lnc-KIF26A-4,lnc-KIF26A-4:2 RNACentral:URS00008BFAB1,RNACentral:URS0000EA8B03 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104209042..104209146 26863196 MeRIP-seq:(Medium) rs1566875560 Functional Loss DEL dbSNP153 1..34 33 - - - 61167 RMVar_ID_61167 Human_SNP_ID_568320701 m1A Human chr14 + 104209087 104209071 104209088 ACCAGCAGAGCTGGGACACCACCAGAGCTGTGAGACCACCAGAGCCGGGACACCACCAGAGCCGG ACCAGCAGAGCTGGGAC_________________ACCACCAGAGCCGGGACACCACCAGAGCCGG CACCACCAGAGCTGTGAG C lnc-KIF26A-4,lnc-KIF26A-4:2 RNACentral:URS00008BFAB1,RNACentral:URS0000EA8B03 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104209042..104209146 26863196 MeRIP-seq:(Medium) rs1357723944 Functional Loss DEL dbSNP153 18..34 33 - - - 61168 RMVar_ID_61168 Human_SNP_ID_568321794 m1A Human chr14 + 104212727 104212714 104212728 GGACCCGGGGTGGGGACGGCGCAGCTGTGTGCATGCAGCTGTGTGTTGTGAGAGGTAGGGTTGGA GGACCCGGGGTGGGGACGGC______________GCAGCTGTGTGTTGTGAGAGGTAGGGTTGGA CGCAGCTGTGTGCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104212676..104212848 26863196 MeRIP-seq:(Medium) rs1380823357 Functional Loss DEL dbSNP153 21..34 33 - - - 61169 RMVar_ID_61169 Human_SNP_ID_568322630 m1A Human chr14 + 104215314 104215298 104215314 GGTCAGTGTATAGGGAGGTCAGTGTGTAGGGAAGTGAGTGTGTAGGGGGGTGTGTGGGGAGATGA GGTCAGTGTATAGGGAG________________GTGAGTGTGTAGGGGGGTGTGTGGGGAGATGA GGTCAGTGTGTAGGGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104214797..104215738 26863196 MeRIP-seq:(Medium) rs1236035517 Functional Loss DEL dbSNP153 18..33 33 - - - 61170 RMVar_ID_61170 Human_SNP_ID_568322637 m1A Human chr14 + 104215314 104215314 104215314 GGTCAGTGTATAGGGAGGTCAGTGTGTAGGGAAGTGAGTGTGTAGGGGGGTGTGTGGGGAGATGA GGTCAGTGTATAGGGAGGTCAGTGTGTAGGGAGGTGAGTGTGTAGGGGGGTGTGTGGGGAGATGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104214797..104215738 26863196 MeRIP-seq:(Medium) rs866345488 Functional Loss SNV dbSNP153 33..33 33 - - - 61171 RMVar_ID_61171 Human_SNP_ID_568348940 m1A Human chr14 + 104304187 104304187 104304187 CCACAGAAATCCCCTCCTCATCTGGCCCTCTGACTCCACCTTTCCACGCTGTCCGTGGGACCAGG CCACAGAAATCCCCTCCTCATCTGGCCCTCTGCCTCCACCTTTCCACGCTGTCCGTGGGACCAGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104304138..104304209 26863196 MeRIP-seq:(Medium) rs1429867546 Functional Loss SNV dbSNP153 33..33 33 - - - 61172 RMVar_ID_61172 Human_SNP_ID_568390589 m1A Human chr14 + 104461654 104461649 104461654 GGGCGGGGGCGGGGCGGGGGGGTGGGCGGGGGAGGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC GGGCGGGGGCGGGGCGGGGGGGTGGGCG_____GGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC GGGGGA G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr14:104461537..104461669;chr14:104461603..104461673 26863196 MeRIP-seq:(Medium) rs1326532269 Functional Loss DEL dbSNP153 29..33 33 - - - 61173 RMVar_ID_61173 Human_SNP_ID_568390592 m1A Human chr14 + 104461654 104461654 104461654 GGGCGGGGGCGGGGCGGGGGGGTGGGCGGGGGAGGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC GGGCGGGGGCGGGGCGGGGGGGTGGGCGGGGGCGGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr14:104461537..104461669;chr14:104461603..104461673 26863196 MeRIP-seq:(Medium) rs188407491 Functional Loss SNV dbSNP153 33..33 33 - - - 61174 RMVar_ID_61174 Human_SNP_ID_568390593 m1A Human chr14 + 104461654 104461654 104461654 GGGCGGGGGCGGGGCGGGGGGGTGGGCGGGGGAGGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC GGGCGGGGGCGGGGCGGGGGGGTGGGCGGGGGGGGGGCGGGGCGGGAGGGCGAGGGCTGTCTCTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr14:104461537..104461669;chr14:104461603..104461673 26863196 MeRIP-seq:(Medium) rs188407491 Functional Loss SNV dbSNP153 33..33 33 - - - 61175 RMVar_ID_61175 Human_SNP_ID_568444687 m1A Human chr14 + 104665140 104665137 104665141 ATGCAAACACACACACACAGACACACACACACAGACACACAGAAACACACAGACACACACAAACC ATGCAAACACACACACACAGACACACACAC____ACACACAGAAACACACAGACACACACAAACC CACAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:104665134..104665232;chr14:104665132..104665222 26863196 MeRIP-seq:(Medium) rs369645874 Functional Loss DEL dbSNP153 31..34 33 - - - 61176 RMVar_ID_61176 Human_SNP_ID_568444688 m1A Human chr14 + 104665140 104665139 104665140 ATGCAAACACACACACACAGACACACACACACAGACACACAGAAACACACAGACACACACAAACC ATGCAAACACACACACACAGACACACACACAC_GACACACAGAAACACACAGACACACACAAACC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:104665134..104665232;chr14:104665132..104665222 26863196 MeRIP-seq:(Medium) rs573726895 Functional Loss DEL dbSNP153 33..33 33 - - - 61177 RMVar_ID_61177 Human_SNP_ID_568444689 m1A Human chr14 + 104665140 104665139 104665141 ATGCAAACACACACACACAGACACACACACACAGACACACAGAAACACACAGACACACACAAACC ATGCAAACACACACACACAGACACACACACAC__ACACACAGAAACACACAGACACACACAAACC CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:104665134..104665232;chr14:104665132..104665222 26863196 MeRIP-seq:(Medium) rs1318252469 Functional Loss DEL dbSNP153 33..34 33 - - - 61178 RMVar_ID_61178 Human_SNP_ID_568448216 m1A Human chr14 + 104677890 104677890 104677890 CTCCTCCCAAGGAGGAGGCAGATGGTGGTGGAAACTCTGCTTCCTCCATTTTCCGGAGCGTGACT CTCCTCCCAAGGAGGAGGCAGATGGTGGTGGACACTCTGCTTCCTCCATTTTCCGGAGCGTGACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104677857..104677955 26863196 MeRIP-seq:(Medium) rs1454210745 Functional Loss SNV dbSNP153 33..33 33 - - - 61179 RMVar_ID_61179 Human_SNP_ID_568448240 m1A Human chr14 + 104677980 104677980 104677980 CCCACGCAGCAGCGCGAAGCCTGCCCTCCCCTACAGCGGAGCCCGGGGACTCCCCAGAACACCCC CCCACGCAGCAGCGCGAAGCCTGCCCTCCCCTGCAGCGGAGCCCGGGGACTCCCCAGAACACCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104677971..104678108 26863196 MeRIP-seq:(Medium) rs1247190194 Functional Loss SNV dbSNP153 33..33 33 - - - 61180 RMVar_ID_61180 Human_SNP_ID_568449408 m1A Human chr14 + 104682315 104682315 104682315 AGGGGCTTTAGCGGGGAAGTGCTGGCCTTCCCACCCCTCCTCTGGAATCTGTCACCTCCCACCCT AGGGGCTTTAGCGGGGAAGTGCTGGCCTTCCCCCCCCTCCTCTGGAATCTGTCACCTCCCACCCT A C AL583722.1 Ensembl:ENSG00000256050 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104682309..104682375 26863196 MeRIP-seq:(Medium) rs908990379 Functional Loss SNV dbSNP153 33..33 33 - - - 61181 RMVar_ID_61181 Human_SNP_ID_568449409 m1A Human chr14 + 104682315 104682315 104682315 AGGGGCTTTAGCGGGGAAGTGCTGGCCTTCCCACCCCTCCTCTGGAATCTGTCACCTCCCACCCT AGGGGCTTTAGCGGGGAAGTGCTGGCCTTCCCGCCCCTCCTCTGGAATCTGTCACCTCCCACCCT A G AL583722.1 Ensembl:ENSG00000256050 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104682309..104682375 26863196 MeRIP-seq:(Medium) rs908990379 Functional Loss SNV dbSNP153 33..33 33 - - - 61182 RMVar_ID_61182 Human_SNP_ID_568451530 m1A Human chr14 - 104689247 104689238 104689247 CTCCGGTGGGACTGGCCTCCCAGGCGCCGCTCACCTCTCTCTGCCCCGGCCCGGGACTCCCGTTC CTCCGGTGGGACTGGCCTCCCAGGCGCCGCTC_________TGCCCCGGCCCGGGACTCCCGTTC AGAGAGAGGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104689205..104689289 26863196 MeRIP-seq:(Medium) rs1219283348 Functional Loss DEL dbSNP153 33..41 33 - - - 61183 RMVar_ID_61183 Human_SNP_ID_568454974 m1A Human chr14 + 104701412 104701412 104701412 GGGCGCACAGCGCAAGTGGGCAGCGCTGAAGGAGAAGCTGGGGCCACAGGATTCGGACCCCACGG GGGCGCACAGCGCAAGTGGGCAGCGCTGAAGGCGAAGCTGGGGCCACAGGATTCGGACCCCACGG A C INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104701340..104701577 26863196 MeRIP-seq:(Medium) rs1475326589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758447,Human_RBP_ID_4309117,Human_RBP_ID_9369568,Human_RBP_ID_18981063 Human_Splice_Rec_1560312,Human_Splice_Rec_1560352,Human_Splice_Rec_1560394 61184 RMVar_ID_61184 Human_SNP_ID_568455629 m1A Human chr14 - 104703401 104703401 104703401 GGGTGCGCGCGCGCAGGTCCTCGGGGCCCAAGATGACGGCGTTGATCACGCTAAGCAGGGTGACC GGGTGCGCGCGCGCAGGTCCTCGGGGCCCAAGGTGACGGCGTTGATCACGCTAAGCAGGGTGACC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr14:104703351..104703475;chr14:104703276..104703400 26863196 MeRIP-seq:(Medium) rs764012283 Functional Loss SNV dbSNP153 33..33 33 - - - 61185 RMVar_ID_61185 Human_SNP_ID_568456961 m1A Human chr14 - 104707457 104707457 104707457 CTTTCAGGATGCTCTCACTCTGGGCGTGGTCCACGGGCTCGCAGGCAGCAGCTGCTGCTGGCTGC CTTTCAGGATGCTCTCACTCTGGGCGTGGTCCTCGGGCTCGCAGGCAGCAGCTGCTGCTGGCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104707408..104707550 26863196 MeRIP-seq:(Medium) rs1566781410 Functional Loss SNV dbSNP153 33..33 33 - - - 61186 RMVar_ID_61186 Human_SNP_ID_568457132 m1A Human chr14 - 104707689 104707686 104707689 TCACAGGAGCCTGGCAGGGGTGGTGGTAGAGGAGGTGCTGGGGGGGCCATGGCCCCCAGGCCTGG TCACAGGAGCCTGGCAGGGGTGGTGGTAGAGG___TGCTGGGGGGGCCATGGCCCCCAGGCCTGG ACCT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:104707576..104707864 26863196 MeRIP-seq:(Medium) rs1325744353 Functional Loss DEL dbSNP153 33..35 33 - - - 61187 RMVar_ID_61187 Human_SNP_ID_568457153 m1A Human chr14 + 104707734 104707734 104707734 CCCCTGCCAGGCTCCTGTGAGTTCCTGCCCCCACCACCTCCACCACTCCCGGGCTTGGGATGCCC CCCCTGCCAGGCTCCTGTGAGTTCCTGCCCCCCCCACCTCCACCACTCCCGGGCTTGGGATGCCC A C INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104707685..104707753 26863196 MeRIP-seq:(Medium) rs1383992230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5127656,Human_RBP_ID_17076443,Human_RBP_ID_18646456,Human_RBP_ID_18937059,Human_RBP_ID_26778581 Human_miRNA_ID_95068,Human_miRNA_ID_1418211 RMVar_hsa_circ_58272,RMVar_hsa_circ_169640,RMVar_hsa_circ_97495,RMVar_hsa_circ_124679,RMVar_hsa_circ_169641,RMVar_hsa_circ_169642,RMVar_hsa_circ_114585 61188 RMVar_ID_61188 Human_SNP_ID_568457274 m1A Human chr14 + 104707948 104707948 104707948 GGGTCCCCAGCCATCGGCGGGTGAACCCACCCACACTGCGCATGAAGAAGCTGAACTGGCAGAAG GGGTCCCCAGCCATCGGCGGGTGAACCCACCCCCACTGCGCATGAAGAAGCTGAACTGGCAGAAG A C INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104707661..104708349 32194978 MeRIP-seq:(Medium) rs1334835727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5563005,Human_RBP_ID_18981082 Human_Splice_Rec_1560325,Human_Splice_Rec_1560365,Human_Splice_Rec_1560401,Human_Splice_Rec_1560431 RMVar_hsa_circ_58272,RMVar_hsa_circ_169640,RMVar_hsa_circ_97495,RMVar_hsa_circ_124679,RMVar_hsa_circ_169641,RMVar_hsa_circ_169642,RMVar_hsa_circ_114585 61189 RMVar_ID_61189 Human_SNP_ID_568459647 m1A Human chr14 - 104714426 104714426 104714426 CCCTCCAAGGGCTGGGGGCACTGGGGATCCTCAGTGGTTAGGACATCGCTGGCATCCACATACCA CCCTCCAAGGGCTGGGGGCACTGGGGATCCTCGGTGGTTAGGACATCGCTGGCATCCACATACCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:104714376..104714525 26863196 MeRIP-seq:(Medium) rs762053888 Functional Loss SNV dbSNP153 33..33 33 - - - 61190 RMVar_ID_61190 Human_SNP_ID_568459688 m1A Human chr14 + 104714549 104714549 104714549 AACCAGCCCCCTGCAGCCGGAAGTTCAAGGCAAGATGCCAAGGATCCCACGTCCTTGCTGGGCGT AACCAGCCCCCTGCAGCCGGAAGTTCAAGGCAGGATGCCAAGGATCCCACGTCCTTGCTGGGCGT A G INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:104714526..104714550 26863196 MeRIP-seq:(Medium) rs1363315841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40513,Human_RBP_ID_442094,Human_RBP_ID_5176669,Human_RBP_ID_9370556,Human_RBP_ID_18469471,Human_RBP_ID_18979953 Human_miRNA_ID_2218240,Human_miRNA_ID_2490570,Human_miRNA_ID_2752654 RMVar_hsa_circ_169640,RMVar_hsa_circ_124679,RMVar_hsa_circ_127102,RMVar_hsa_circ_169645,RMVar_hsa_circ_20129,RMVar_hsa_circ_48026 61191 RMVar_ID_61191 Human_SNP_ID_568459717 m1A Human chr14 - 104714617 104714617 104714617 GTCTGGCACCACGGCTGTGGACAGCGTCCTCCAGCCCCTCACTTGTGCTGTCGGCCTCGGCCTGG GTCTGGCACCACGGCTGTGGACAGCGTCCTCCCGCCCCTCACTTGTGCTGTCGGCCTCGGCCTGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:104714601..104714625 26863196 MeRIP-seq:(Medium) rs776546949 Functional Loss SNV dbSNP153 33..33 33 - - - 61192 RMVar_ID_61192 Human_SNP_ID_568461115 m1A Human chr14 + 104718352 104718352 104718352 GGGGCCGTCTGGGTGGCGGGAGCTGTTGGGGCAGGGCTGAGCGCCCTCAGCAGCCCACTGGAGAA GGGGCCGTCTGGGTGGCGGGAGCTGTTGGGGCGGGGCTGAGCGCCCTCAGCAGCCCACTGGAGAA A G INF2 Ensembl:ENSG00000203485 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:104718301..104718463 26863196 MeRIP-seq:(Medium) rs4247032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3468278,Human_RBP_ID_5176873,Human_RBP_ID_8181082,Human_RBP_ID_9417851,Human_RBP_ID_18457736 RMVar_hsa_circ_127102,RMVar_hsa_circ_169645 61193 RMVar_ID_61193 Human_SNP_ID_568461159 m1A Human chr14 + 104718473 104718473 104718473 CTGCAGGGGGTGGCAGTGGGGATGAATGAGTAAGGACAGAGTGCAGCCTGGGTCTCAGACAGGGG CTGCAGGGGGTGGCAGTGGGGATGAATGAGTAGGGACAGAGTGCAGCCTGGGTCTCAGACAGGGG A G INF2 Ensembl:ENSG00000203485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104718270..104718592 26863196 MeRIP-seq:(Medium) rs1393492686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5176671,Human_RBP_ID_26768574 RMVar_hsa_circ_127102,RMVar_hsa_circ_169645 61194 RMVar_ID_61194 Human_SNP_ID_568462535 m1A Human chr14 + 104722925 104722925 104722925 AAGAGGGGACTGGGGACATGGGTGCAGGGGGCAGGAGGCCAGGCTTCAAACAGCCCCTCTCCCCC AAGAGGGGACTGGGGACATGGGTGCAGGGGGCGGGAGGCCAGGCTTCAAACAGCCCCTCTCCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104722874..104722963 26863196 MeRIP-seq:(Medium) rs767488980 Functional Loss SNV dbSNP153 33..33 33 - - - 61195 RMVar_ID_61195 Human_SNP_ID_568463134 m1A Human chr14 + 104724605 104724605 104724605 GCCTTCCTTCCGGGAGCACCTTTCCCAGGGCCACCCCACCCACGCACGCACACGCACCACTCACA GCCTTCCTTCCGGGAGCACCTTTCCCAGGGCCGCCCCACCCACGCACGCACACGCACCACTCACA A G ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104724602..104724698 26863196 MeRIP-seq:(Medium) rs117084961 Functional Loss SNV dbSNP153 33..33 33 - - - 61196 RMVar_ID_61196 Human_SNP_ID_568463463 m1A Human chr14 + 104725639 104725637 104725639 CCTAAGCAGCAGGCAAGCACATCCCTCGCTCCAGAGATCCCCCAGGTCCTAGAGGTGGTCCTCAG CCTAAGCAGCAGGCAAGCACATCCCTCGCTC__GAGATCCCCCAGGTCCTAGAGGTGGTCCTCAG CCA C ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104725637..104725702 26863196 MeRIP-seq:(Medium) rs1390576295 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_24411000 61197 RMVar_ID_61197 Human_SNP_ID_568463464 m1A Human chr14 + 104725639 104725639 104725639 CCTAAGCAGCAGGCAAGCACATCCCTCGCTCCAGAGATCCCCCAGGTCCTAGAGGTGGTCCTCAG CCTAAGCAGCAGGCAAGCACATCCCTCGCTCCGGAGATCCCCCAGGTCCTAGAGGTGGTCCTCAG A G ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104725637..104725702 26863196 MeRIP-seq:(Medium) rs952624579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24411000 61198 RMVar_ID_61198 Human_SNP_ID_568464241 m1A Human chr14 + 104728523 104728523 104728523 TTGAAGGAATGAATGAATGGTGGGAGCCTGCAAGCAGAGCCCAGAAGGGAGTGAAGCAGTGTAAG TTGAAGGAATGAATGAATGGTGGGAGCCTGCATGCAGAGCCCAGAAGGGAGTGAAGCAGTGTAAG A T ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104728516..104728628 26863196 MeRIP-seq:(Medium) rs958253314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3467803,Human_RBP_ID_8078353,Human_RBP_ID_18418203 61199 RMVar_ID_61199 Human_SNP_ID_568464627 m1A Human chr14 - 104729559 104729557 104729560 CCCACCACGCCGACGCCACGCTCCTCCCCACCACGCCGACGCCACGCTCCTCCCCACGACGCCGA CCCACCACGCCGACGCCACGCTCCTCCCCAC___GCCGACGCCACGCTCCTCCCCACGACGCCGA CGTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:104728932..104729625;chr14:104728902..104729775;chr14:104729448..104729748 26863196 MeRIP-seq:(Medium) rs1428946311 Functional Loss DEL dbSNP153 32..34 33 - - - 61200 RMVar_ID_61200 Human_SNP_ID_568464687 m1A Human chr14 + 104729893 104729664 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG _________________________________TGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG CGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCA C ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs1566794087 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 61201 RMVar_ID_61201 Human_SNP_ID_568464694 m1A Human chr14 - 104729715 104729693 104729716 CTCCCCACGACGCCGACGCCACGCTCCTCCCGACGCCGACGCCACGCTCCTCCCCACGACGCCGA CTCCCCACGACGCCGACGCCACGCTCCTCCC_______________________CACGACGCCGA GGGGAGGAGCGTGGCGTCGGCGTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729676..104729775 26863196 MeRIP-seq:(Medium) rs1460556833 Functional Loss DEL dbSNP153 32..54 33 - - - 61202 RMVar_ID_61202 Human_SNP_ID_568464700 m1A Human chr14 + 104729720 104729720 104729720 GTCGTGGGGAGGAGCGTGGCGTCGGCGTCGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCG GTCGTGGGGAGGAGCGTGGCGTCGGCGTCGGGGGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCG A G ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104729015..104729776 26863196 MeRIP-seq:(Medium) rs1390153115 Functional Loss SNV dbSNP153 33..33 33 - - - 61203 RMVar_ID_61203 Human_SNP_ID_568464729 m1A Human chr14 + 104729893 104729791 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG _________________________________TGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG CGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCA C ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs1566794160 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 61204 RMVar_ID_61204 Human_SNP_ID_568464778 m1A Human chr14 - 104729888 104729888 104729888 TTGCCACCCCACAGCTCCTCCCCACCATGCCGACGCCACGCTCCTCCCCACGACGCCGACGCCAC TTGCCACCCCACAGCTCCTCCCCACCATGCCGGCGCCACGCTCCTCCCCACGACGCCGACGCCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104729851..104730189 26863196 MeRIP-seq:(Medium) rs962302121 Functional Loss SNV dbSNP153 33..33 33 - - - 61205 RMVar_ID_61205 Human_SNP_ID_568464783 m1A Human chr14 + 104729893 104729893 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCCTGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG A C ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs80097179 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 61206 RMVar_ID_61206 Human_SNP_ID_568464784 m1A Human chr14 + 104729893 104729893 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG A G ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs80097179 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 61207 RMVar_ID_61207 Human_SNP_ID_568467425 m1A Human chr14 - 104738353 104738353 104738353 ACCCCGTTGCCTGCATGAGAGACAGAGGCATGAGAGACAGAGTTGTGTCCCAGACACTGGAAAAC ACCCCGTTGCCTGCATGAGAGACAGAGGCATGCGAGACAGAGTTGTGTCCCAGACACTGGAAAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104738350..104738471 26863196 MeRIP-seq:(Medium) rs1292305364 Functional Loss SNV dbSNP153 33..33 33 - - - 61208 RMVar_ID_61208 Human_SNP_ID_568469067 m1A Human chr14 + 104743172 104743172 104743172 GGCTCGACCTGATGATTCTAAGATATGCTCACATGGTCAACGGATTCACTGCGTAAGCAACCCAT GGCTCGACCTGATGATTCTAAGATATGCTCACGTGGTCAACGGATTCACTGCGTAAGCAACCCAT A G ADSS1 Ensembl:ENSG00000185100 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104743124..104743229 26863196 MeRIP-seq:(Medium) rs759674422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9370563 Human_Splice_Rec_1560497,Human_Splice_Rec_1560537,Human_Splice_Rec_1560561,Human_Splice_Rec_1560581,Human_Splice_Rec_1560591 RMVar_hsa_circ_74246,RMVar_hsa_circ_28385 61209 RMVar_ID_61209 Human_SNP_ID_568472012 m1A Human chr14 + 104753214 104753214 104753214 TAGCTCCCGGCCCCGCGGCCATGCCCAAGCGGAGCTGCCCCTTCGCGGACGTGGCCCCGCTACAG TAGCTCCCGGCCCCGCGGCCATGCCCAAGCGGGGCTGCCCCTTCGCGGACGTGGCCCCGCTACAG A G SIVA1 Ensembl:ENSG00000184990 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104753151..104753372 26863196 MeRIP-seq:(Medium) rs765580260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442106,Human_RBP_ID_1489469,Human_RBP_ID_4284156,Human_RBP_ID_5112609,Human_RBP_ID_5463171,Human_RBP_ID_8400449,Human_RBP_ID_8793277,Human_RBP_ID_9323925,Human_RBP_ID_17651481,Human_RBP_ID_22439491,Human_RBP_ID_23613918 Human_miRNA_ID_2385027 RMVar_hsa_circ_104602,RMVar_hsa_circ_169648 61210 RMVar_ID_61210 Human_SNP_ID_568472047 m1A Human chr14 + 104753251 104753251 104753251 CCCCTTCGCGGACGTGGCCCCGCTACAGCTCAAGGTCCGCGTGAGCCAGAGGGAGTTGAGCCGCG CCCCTTCGCGGACGTGGCCCCGCTACAGCTCAGGGTCCGCGTGAGCCAGAGGGAGTTGAGCCGCG A G SIVA1 Ensembl:ENSG00000184990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104753202..104753288 26863196 MeRIP-seq:(Medium) rs760022416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442107,Human_RBP_ID_813757,Human_RBP_ID_1489469,Human_RBP_ID_4284156,Human_RBP_ID_5112491,Human_RBP_ID_5315737,Human_RBP_ID_8400449,Human_RBP_ID_9324147,Human_RBP_ID_17651481,Human_RBP_ID_18646493,Human_RBP_ID_22438981,Human_RBP_ID_26921051,Human_RBP_ID_27224459 Human_Splice_Rec_1560607,Human_Splice_Rec_1560611,Human_Splice_Rec_1560617,Human_Splice_Rec_1560621,Human_Splice_Rec_1560627,Human_Splice_Rec_1560637,Human_Splice_Rec_1560639 Human_miRNA_ID_2083795,Human_miRNA_ID_2391832,Human_miRNA_ID_2956121 RMVar_hsa_circ_104602,RMVar_hsa_circ_169648 61211 RMVar_ID_61211 Human_SNP_ID_568472130 m1A Human chr14 + 104753466 104753466 104753466 CGCGTTCCCGGAAGCTGGGAGGCCGCGGGGACACAAGCTGGCCACGCCCAGGGCTGGGGTCAGTG CGCGTTCCCGGAAGCTGGGAGGCCGCGGGGACGCAAGCTGGCCACGCCCAGGGCTGGGGTCAGTG A G SIVA1 Ensembl:ENSG00000184990 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104753462..104753564 26863196 MeRIP-seq:(Medium) rs944397303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5353457 RMVar_hsa_circ_104602,RMVar_hsa_circ_169648 61212 RMVar_ID_61212 Human_SNP_ID_568472327 m1A Human chr14 + 104753918 104753918 104753918 CAGGTTTGTGCAGGCGCACCTGCAGGGATGGCACGGAAGGCTTCTTGGAAGAACAGTCTGAGCGG CAGGTTTGTGCAGGCGCACCTGCAGGGATGGCGCGGAAGGCTTCTTGGAAGAACAGTCTGAGCGG A G SIVA1 Ensembl:ENSG00000184990 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104753916..104754074 26863196 MeRIP-seq:(Medium) rs1348198816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18646495 RMVar_hsa_circ_104602,RMVar_hsa_circ_169648 61213 RMVar_ID_61213 Human_SNP_ID_568473134 m1A Human chr14 - 104756674 104756674 104756674 ACACACTGCCCGCACAGGGCTCGCTCACACTGACCGCAGACCGCCTTCCCATCCACGGCTCGCAC ACACACTGCCCGCACAGGGCTCGCTCACACTGCCCGCAGACCGCCTTCCCATCCACGGCTCGCAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104756581..104756681 32194978 MeRIP-seq:(Medium) rs1298763444 Functional Loss SNV dbSNP153 33..33 33 - - - 61214 RMVar_ID_61214 Human_SNP_ID_568476567 m1A Human chr14 - 104769449 104769449 104769449 GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCACCACGGCGTTTTTTTACAACATTCAACTTTAG GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCTCCACGGCGTTTTTTTACAACATTCAACTTTAG T A AKT1 Ensembl:ENSG00000142208 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104769398..104769716 26863196 MeRIP-seq:(Medium) rs1186786985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442136 Human_miRNA_ID_204416 RMVar_hsa_circ_78825,RMVar_hsa_circ_108929,RMVar_hsa_circ_169651,RMVar_hsa_circ_169652 61215 RMVar_ID_61215 Human_SNP_ID_568476568 m1A Human chr14 - 104769449 104769449 104769449 GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCACCACGGCGTTTTTTTACAACATTCAACTTTAG GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCGCCACGGCGTTTTTTTACAACATTCAACTTTAG T C AKT1 Ensembl:ENSG00000142208 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104769398..104769716 26863196 MeRIP-seq:(Medium) rs1186786985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442136 Human_miRNA_ID_204416 RMVar_hsa_circ_78825,RMVar_hsa_circ_108929,RMVar_hsa_circ_169651,RMVar_hsa_circ_169652 61216 RMVar_ID_61216 Human_SNP_ID_568476569 m1A Human chr14 - 104769449 104769449 104769449 GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCACCACGGCGTTTTTTTACAACATTCAACTTTAG GCCTCCTGGCCAGACGCTGCCGCTGCCGCTGCCCCACGGCGTTTTTTTACAACATTCAACTTTAG T G AKT1 Ensembl:ENSG00000142208 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104769398..104769716 26863196 MeRIP-seq:(Medium) rs1186786985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442136 Human_miRNA_ID_204416 RMVar_hsa_circ_78825,RMVar_hsa_circ_108929,RMVar_hsa_circ_169651,RMVar_hsa_circ_169652 61217 RMVar_ID_61217 Human_SNP_ID_568477407 m1A Human chr14 - 104772304 104772304 104772304 CACGCATGCTCCCCACATATCCACACTCACGCATGCACGTGGCACGCTCGCCAGATTTCCCACAC CACGCATGCTCCCCACATATCCACACTCACGCCTGCACGTGGCACGCTCGCCAGATTTCCCACAC T G AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104772303..104772408 26863196 MeRIP-seq:(Medium) rs1461606439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41483,RMVar_hsa_circ_78825,RMVar_hsa_circ_108929,RMVar_hsa_circ_92902,RMVar_hsa_circ_125525,RMVar_hsa_circ_169651,RMVar_hsa_circ_169652,RMVar_hsa_circ_372085,RMVar_hsa_circ_103082,RMVar_hsa_circ_87438,RMVar_hsa_circ_169654,RMVar_hsa_circ_169656,RMVar_hsa_circ_169658,RMVar_hsa_circ_23769,RMVar_hsa_circ_169657,RMVar_hsa_circ_169655 61218 RMVar_ID_61218 Human_SNP_ID_568477486 m1A Human chr14 + 104772449 104772449 104772449 ATGATCTCCTTGGCGTCCTCGGAGCCCCCGCCAAGCCTGCAGGCAGGAAACAAGGCCACAGTGTC ATGATCTCCTTGGCGTCCTCGGAGCCCCCGCCGAGCCTGCAGGCAGGAAACAAGGCCACAGTGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104772288..104773100 32194978 MeRIP-seq:(Medium) rs1049525123 Functional Loss SNV dbSNP153 33..33 33 - - - 61219 RMVar_ID_61219 Human_SNP_ID_568477701 m1A Human chr14 + 104773088 104773088 104773088 AGTCCACTGCACGGCCGTAGTCATTGTCCTCCAGCACCTGCACGGGTGGCAGATGGGCAGGACTC AGTCCACTGCACGGCCGTAGTCATTGTCCTCCGGCACCTGCACGGGTGGCAGATGGGCAGGACTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104772940..104773122 26863196 MeRIP-seq:(Medium) rs1454909926 Functional Loss SNV dbSNP153 33..33 33 - - - 61220 RMVar_ID_61220 Human_SNP_ID_568478007 m1A Human chr14 + 104773888 104773888 104773888 CCACCATGGGCGGCCCACAGGCCGCGAAGTCCATCCCCCGCAGCCCCAGCCCCTACCTCGCCCCC CCACCATGGGCGGCCCACAGGCCGCGAAGTCCGTCCCCCGCAGCCCCAGCCCCTACCTCGCCCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104773884..104774084 32194978 MeRIP-seq:(Medium) rs764437439 Functional Loss SNV dbSNP153 33..33 33 - - - 61221 RMVar_ID_61221 Human_SNP_ID_568478050 m1A Human chr14 - 104773998 104773992 104773998 GGCTGCCGTCCTGCCTGTGGGGCCGCAGTTCCAGCTCCCCTTCCTTGCAGGCCCTGAAGTACTCT GGCTGCCGTCCTGCCTGTGGGGCCGCAGTTCC______CCTTCCTTGCAGGCCCTGAAGTACTCT GGGAGCT G AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104773995..104774234 26863196 MeRIP-seq:(Medium) rs1566817049 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_880711,Human_RBP_ID_5352519,Human_RBP_ID_18161180,Human_RBP_ID_19066572,Human_RBP_ID_22540155,Human_RBP_ID_22648909 Human_Splice_Rec_1560661,Human_Splice_Rec_1560687,Human_Splice_Rec_1560715,Human_Splice_Rec_1560759,Human_Splice_Rec_1560785,Human_Splice_Rec_1560813,Human_Splice_Rec_1560853,Human_Splice_Rec_1560889 RMVar_hsa_circ_434,RMVar_hsa_circ_41483,RMVar_hsa_circ_108929,RMVar_hsa_circ_169651,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_91939,RMVar_hsa_circ_169660,RMVar_hsa_circ_120303,RMVar_hsa_circ_169661 61222 RMVar_ID_61222 Human_SNP_ID_568478455 m1A Human chr14 + 104775152 104775152 104775152 AGCGGCCTGTGGCCTTCTCCTTCACCAGGATCACCTTGCCGAAAGTGCCCTTGCCCAGCAGCTTC AGCGGCCTGTGGCCTTCTCCTTCACCAGGATCCCCTTGCCGAAAGTGCCCTTGCCCAGCAGCTTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104774332..104775928 32194978 MeRIP-seq:(Medium) rs1244026143 Functional Loss SNV dbSNP153 33..33 33 - - - 61223 RMVar_ID_61223 Human_SNP_ID_568478648 m1A Human chr14 - 104775737 104775735 104775738 GGCTGACGGCCTCAAGAAGCAGGAGGAGGAGGAGATGGACTTCCGGTCGGGCTCACCCAGTGACA GGCTGACGGCCTCAAGAAGCAGGAGGAGGAG___ATGGACTTCCGGTCGGGCTCACCCAGTGACA TCTC T AKT1 Ensembl:ENSG00000142208 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104775686..104775845 26863196 MeRIP-seq:(Medium) rs768025881 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3945163,Human_RBP_ID_18981124,Human_RBP_ID_22926374,Human_RBP_ID_26324786,Human_RBP_ID_26431901 Human_Splice_Rec_1560654,Human_Splice_Rec_1560655,Human_Splice_Rec_1560680,Human_Splice_Rec_1560681,Human_Splice_Rec_1560708,Human_Splice_Rec_1560709,Human_Splice_Rec_1560752,Human_Splice_Rec_1560753,Human_Splice_Rec_1560778,Human_Splice_Rec_1560779,Human_Splice_Rec_1560806,Human_Splice_Rec_1560807,Human_Splice_Rec_1560846,Human_Splice_Rec_1560847,Human_Splice_Rec_1560882,Human_Splice_Rec_1560883,Human_Splice_Rec_1560902,Human_Splice_Rec_1560903,Human_Splice_Rec_1560916,Human_Splice_Rec_1560917 Human_miRNA_ID_2018262,Human_miRNA_ID_2018263 RMVar_hsa_circ_41483,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_89665,RMVar_hsa_circ_101376,RMVar_hsa_circ_125927,RMVar_hsa_circ_92821,RMVar_hsa_circ_169663,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_169664,RMVar_hsa_circ_169662,RMVar_hsa_circ_369007 61224 RMVar_ID_61224 Human_SNP_ID_568480930 m1A Human chr14 + 104782235 104782235 104782235 CCCCGCTGCTCACGCCCACCCGCCTGCATGCCAGTCTGGAGCTGTCGGCCCCTGATGGAGTGCCT CCCCGCTGCTCACGCCCACCCGCCTGCATGCCGGTCTGGAGCTGTCGGCCCCTGATGGAGTGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104782232..104782437 26863196 MeRIP-seq:(Medium) rs1193116545 Functional Loss SNV dbSNP153 33..33 33 - - - 61225 RMVar_ID_61225 Human_SNP_ID_568480931 m1A Human chr14 + 104782235 104782235 104782235 CCCCGCTGCTCACGCCCACCCGCCTGCATGCCAGTCTGGAGCTGTCGGCCCCTGATGGAGTGCCT CCCCGCTGCTCACGCCCACCCGCCTGCATGCCTGTCTGGAGCTGTCGGCCCCTGATGGAGTGCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104782232..104782437 26863196 MeRIP-seq:(Medium) rs1193116545 Functional Loss SNV dbSNP153 33..33 33 - - - 61226 RMVar_ID_61226 Human_SNP_ID_568480938 m1A Human chr14 - 104782258 104782258 104782258 GGAGTGGCAGCTGGCAGGATGGGAGGCACTCCATCAGGGGCCGACAGCTCCAGACTGGCATGCAG GGAGTGGCAGCTGGCAGGATGGGAGGCACTCCCTCAGGGGCCGACAGCTCCAGACTGGCATGCAG T G AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104782256..104782359 26863196 MeRIP-seq:(Medium) rs943995645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3467814,Human_RBP_ID_8181111,Human_RBP_ID_22737541 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 61227 RMVar_ID_61227 Human_SNP_ID_568481490 m1A Human chr14 - 104784102 104784045 104784102 GCCCAGGGGGCCAGCAGGAGGGTGAGACTGGAACTGCTGCTTCCCCGCTGCCGAGGGAACCGGCC GCCCAGGGGGCCAGCAGGAGGGTGAGACTGGA_________________________________ CTCCGGTCCCACCCTCCTGCCCCATGGCCGGTTCCCTCGGCAGCGGGGAAGCAGCAGT C AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104784099..104784164 26863196 MeRIP-seq:(Medium) rs1566823033 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5177693,Human_RBP_ID_8230662,Human_RBP_ID_9324155,Human_RBP_ID_17205801 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 61228 RMVar_ID_61228 Human_SNP_ID_568481514 m1A Human chr14 - 104784102 104784102 104784102 GCCCAGGGGGCCAGCAGGAGGGTGAGACTGGAACTGCTGCTTCCCCGCTGCCGAGGGAACCGGCC GCCCAGGGGGCCAGCAGGAGGGTGAGACTGGAGCTGCTGCTTCCCCGCTGCCGAGGGAACCGGCC T C AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104784099..104784164 26863196 MeRIP-seq:(Medium) rs113750262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5177693,Human_RBP_ID_8230662,Human_RBP_ID_9324155,Human_RBP_ID_17205801 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 61229 RMVar_ID_61229 Human_SNP_ID_568483569 m1A Human chr14 - 104791530 104791528 104791530 AGGAGTGACCGAGATGAGATGCTGGGGGAATCAGGGGTGTGGCTGGCTGTGTGTTTGGAGTGTTT AGGAGTGACCGAGATGAGATGCTGGGGGAATC__GGGTGTGGCTGGCTGTGTGTTTGGAGTGTTT CCT C AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104791526..104791635 26863196 MeRIP-seq:(Medium) rs750022693 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5141214,Human_RBP_ID_8230673,Human_RBP_ID_22696679,Human_RBP_ID_23614013 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 61230 RMVar_ID_61230 Human_SNP_ID_568483930 m1A Human chr14 - 104792706 104792706 104792706 CCTTTGCTTCTCCCAGAGGCTGTGGCCAGGCCAGCTGGGCTCGGGGAGCGCCAGCCTGAGAGGAG CCTTTGCTTCTCCCAGAGGCTGTGGCCAGGCCCGCTGGGCTCGGGGAGCGCCAGCCTGAGAGGAG T G AKT1 Ensembl:ENSG00000142208 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:104786307..104793335;chr14:104792541..104793335;chr14:104792551..104792778 26863196 MeRIP-seq:(Medium) rs796352104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231237,Human_RBP_ID_756520,Human_RBP_ID_882680,Human_RBP_ID_4308149,Human_RBP_ID_22439497,Human_RBP_ID_22578024,Human_RBP_ID_22649322,Human_RBP_ID_24558422 Human_Splice_Rec_1560674,Human_Splice_Rec_1560702,Human_Splice_Rec_1560746,Human_Splice_Rec_1560772,Human_Splice_Rec_1560800,Human_Splice_Rec_1560876,Human_Splice_Rec_1560922 Human_miRNA_ID_2937533,Human_miRNA_ID_2937534 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 61231 RMVar_ID_61231 Human_SNP_ID_568484035 m1A Human chr14 - 104793128 104793128 104793128 CCTGGAGGAGGCAGCCTGTCAGCTGGTGCATCAGGTTAGGGAGGCTGGGAAGGCCTTTTGGGGAT CCTGGAGGAGGCAGCCTGTCAGCTGGTGCATCGGGTTAGGGAGGCTGGGAAGGCCTTTTGGGGAT T C AKT1 Ensembl:ENSG00000142208 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104793126..104793254 26863196 MeRIP-seq:(Medium) rs1228903487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1560700,Human_Splice_Rec_1560701,Human_Splice_Rec_1560745,Human_Splice_Rec_1560771,Human_Splice_Rec_1560799,Human_Splice_Rec_1560921 RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_125927,RMVar_hsa_circ_169666 61232 RMVar_ID_61232 Human_SNP_ID_568484311 m1A Human chr14 + 104794181 104794170 104794181 AGGATGGAAAGCAGGCCAGACTCGAGGAAGGCACCGCAGGACTCCGAGGGCAGGGCTCCGAGCCG AGGATGGAAAGCAGGCCAGACT___________CCGCAGGACTCCGAGGGCAGGGCTCCGAGCCG TCGAGGAAGGCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104794178..104794262 26863196 MeRIP-seq:(Medium) rs1025957871 Functional Loss DEL dbSNP153 23..33 33 - - - 61233 RMVar_ID_61233 Human_SNP_ID_568484313 m1A Human chr14 + 104794173 104794171 104794174 TACTTAGCAGGATGGAAAGCAGGCCAGACTCGAGGAAGGCACCGCAGGACTCCGAGGGCAGGGCT TACTTAGCAGGATGGAAAGCAGGCCAGACTC___GAAGGCACCGCAGGACTCCGAGGGCAGGGCT CGAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104794171..104794261 26863196 MeRIP-seq:(Medium) rs1257797141 Functional Loss DEL dbSNP153 32..34 33 - - - 61234 RMVar_ID_61234 Human_SNP_ID_568484315 m1A Human chr14 + 104794173 104794173 104794173 TACTTAGCAGGATGGAAAGCAGGCCAGACTCGAGGAAGGCACCGCAGGACTCCGAGGGCAGGGCT TACTTAGCAGGATGGAAAGCAGGCCAGACTCGCGGAAGGCACCGCAGGACTCCGAGGGCAGGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104794171..104794261 26863196 MeRIP-seq:(Medium) rs1230331739 Functional Loss SNV dbSNP153 33..33 33 - - - 61235 RMVar_ID_61235 Human_SNP_ID_568487841 m1A Human chr14 - 104806438 104806436 104806439 ATTGAAGATGGGACTGAGGTGGGGATGAAAGAAGTCATAGAAAACCAGGGCAGAGCCTCTGTGGG ATTGAAGATGGGACTGAGGTGGGGATGAAAG___TCATAGAAAACCAGGGCAGAGCCTCTGTGGG ACTT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104806423..104806781 26863196 MeRIP-seq:(Medium) rs370675066 Functional Loss DEL dbSNP153 32..34 33 - - - 61236 RMVar_ID_61236 Human_SNP_ID_568493121 m1A Human chr14 + 104824827 104824824 104824827 TATGGTTGGATGGTGAATGGTTGGATGAATTGATGGATGGATGGTAGGATAGGTGAATGGTTGGA TATGGTTGGATGGTGAATGGTTGGATGAAT___TGGATGGATGGTAGGATAGGTGAATGGTTGGA TTGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104824816..104824912 26863196 MeRIP-seq:(Medium) rs1483263834 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23614053 61237 RMVar_ID_61237 Human_SNP_ID_568493377 m1A Human chr14 + 104825797 104825797 104825797 AGGATTGGCGGAGATGGCCTCGCTGACTGGGAATATTTGAGCAGAGGCAGGAAATGGCTGGGGCG AGGATTGGCGGAGATGGCCTCGCTGACTGGGACTATTTGAGCAGAGGCAGGAAATGGCTGGGGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104825790..104825885 26863196 MeRIP-seq:(Medium) rs1267943743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17845494 61238 RMVar_ID_61238 Human_SNP_ID_568493424 m1A Human chr14 + 104826034 104826034 104826034 AGCTGCAGGAAGGTTTGATCCCCGGAGAGACCAGATCGGGCTTGAGCTCTGACCGCAACCCCTGG AGCTGCAGGAAGGTTTGATCCCCGGAGAGACCGGATCGGGCTTGAGCTCTGACCGCAACCCCTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104826019..104826103 26863196 MeRIP-seq:(Medium) rs1035917937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6328877 61239 RMVar_ID_61239 Human_SNP_ID_568496374 m1A Human chr14 - 104836779 104836779 104836779 GTGGTGCCTTCCGCGGAGGTTTCGGCAGTGGCATCCGGGGCCGGGGTCGCGGCCGTGGACGGGGC GTGGTGCCTTCCGCGGAGGTTTCGGCAGTGGCCTCCGGGGCCGGGGTCGCGGCCGTGGACGGGGC T G RPS2P4 Ensembl:ENSG00000196183 Pseudogene exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:104836772..104836954 26863196 MeRIP-seq:(Medium) rs1401563046 Functional Loss SNV dbSNP153 33..33 33 - - - 61240 RMVar_ID_61240 Human_SNP_ID_568502301 m1A Human chr14 - 104859158 104859158 104859158 GATGGAGGGTGGAGATGGTGAGTGGTGATAGAAGGTGGAGATGAATGGTGGCGATGGACGGTGGA GATGGAGGGTGGAGATGGTGAGTGGTGATAGATGGTGGAGATGAATGGTGGCGATGGACGGTGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104858900..104859312 26863196 MeRIP-seq:(Medium) rs1271988693 Functional Loss SNV dbSNP153 33..33 33 - - - 61241 RMVar_ID_61241 Human_SNP_ID_568502302 m1A Human chr14 - 104859158 104859158 104859158 GATGGAGGGTGGAGATGGTGAGTGGTGATAGAAGGTGGAGATGAATGGTGGCGATGGACGGTGGA GATGGAGGGTGGAGATGGTGAGTGGTGATAGAGGGTGGAGATGAATGGTGGCGATGGACGGTGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104858900..104859312 26863196 MeRIP-seq:(Medium) rs1271988693 Functional Loss SNV dbSNP153 33..33 33 - - - 61242 RMVar_ID_61242 Human_SNP_ID_568502797 m1A Human chr14 + 104860473 104860468 104860474 CCCTCCATCTCCACCATCCATCACAACCATTCATCTCTACTGTCCATCACCACCCTCCATTTCCA CCCTCCATCTCCACCATCCATCACAACC______CTCTACTGTCCATCACCACCCTCCATTTCCA CATTCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104860463..104860589 26863196 MeRIP-seq:(Medium) rs1209092698 Functional Loss DEL dbSNP153 29..34 33 - - - 61243 RMVar_ID_61243 Human_SNP_ID_568503152 m1A Human chr14 + 104861245 104861245 104861245 CCGTCCGTCACTACCCTCTGTCTCCACTGTCCATGTCCACCATCCATCACTACCCTCCGTCTCCA CCGTCCGTCACTACCCTCTGTCTCCACTGTCCCTGTCCACCATCCATCACTACCCTCCGTCTCCA A C lnc-CEP170B-3 RNACentral:URS00008B781D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104860821..104862645 26863196 MeRIP-seq:(Medium) rs931469895 Functional Loss SNV dbSNP153 33..33 33 - - - 61244 RMVar_ID_61244 Human_SNP_ID_568503419 m1A Human chr14 - 104861894 104861894 104861894 GGGTGGTGATGGACGGTGGACACAGACGGTGGAGATAGAGGGTGGTGATGGACGGTGGACACGGA GGGTGGTGATGGACGGTGGACACAGACGGTGGGGATAGAGGGTGGTGATGGACGGTGGACACGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104861856..104861957 26863196 MeRIP-seq:(Medium) rs112567182 Functional Loss SNV dbSNP153 33..33 33 - - - 61245 RMVar_ID_61245 Human_SNP_ID_568504528 m1A Human chr14 + 104865467 104865444 104865468 AGCTGGGGAACAAGCCGGGGACCAAGCCGGGGACCAAGCCGGGGACTAAGGCGAGCCGGAGACCG AGCTGGGGAA________________________CAAGCCGGGGACTAAGGCGAGCCGGAGACCG ACAAGCCGGGGACCAAGCCGGGGAC A CEP170B Ensembl:ENSG00000099814 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104865349..104865572 26863196 MeRIP-seq:(Medium) rs1047945175 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_882328,Human_RBP_ID_3469042,Human_RBP_ID_4308154,Human_RBP_ID_5353489,Human_RBP_ID_5463837,Human_RBP_ID_5646007,Human_RBP_ID_8230674,Human_RBP_ID_9418332,Human_RBP_ID_18418244,Human_RBP_ID_22415078,Human_RBP_ID_22696551,Human_RBP_ID_22711527,Human_RBP_ID_26778599 Human_Splice_Rec_1560933,Human_Splice_Rec_1560965,Human_Splice_Rec_1560995 61246 RMVar_ID_61246 Human_SNP_ID_568504529 m1A Human chr14 + 104865467 104865444 104865468 AGCTGGGGAACAAGCCGGGGACCAAGCCGGGGACCAAGCCGGGGACTAAGGCGAGCCGGAGACCG AGCTGGGGAACAAGCCGGGGAC____________CAAGCCGGGGACTAAGGCGAGCCGGAGACCG ACAAGCCGGGGACCAAGCCGGGGAC ACAAGCCGGGGAC CEP170B Ensembl:ENSG00000099814 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104865349..104865572 26863196 MeRIP-seq:(Medium) rs1047945175 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_882328,Human_RBP_ID_3469042,Human_RBP_ID_4308154,Human_RBP_ID_5353489,Human_RBP_ID_5463837,Human_RBP_ID_5646007,Human_RBP_ID_8230674,Human_RBP_ID_9418332,Human_RBP_ID_18418244,Human_RBP_ID_22415078,Human_RBP_ID_22696551,Human_RBP_ID_22711527,Human_RBP_ID_26778599 Human_Splice_Rec_1560933,Human_Splice_Rec_1560965,Human_Splice_Rec_1560995 61247 RMVar_ID_61247 Human_SNP_ID_568505266 m1A Human chr14 + 104868393 104868393 104868393 ATGTGTCCAGGGGGCTAAGAACCAGGCCAGGGAGCCCCACTCTAACAATCCCCTCTTCCCCAGGG ATGTGTCCAGGGGGCTAAGAACCAGGCCAGGGTGCCCCACTCTAACAATCCCCTCTTCCCCAGGG A T CEP170B Ensembl:ENSG00000099814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104868391..104868645 26863196 MeRIP-seq:(Medium) rs1453486956 Functional Loss SNV dbSNP153 33..33 33 - - - 61248 RMVar_ID_61248 Human_SNP_ID_568507251 m1A Human chr14 - 104874177 104874177 104874177 CTTCCTACCTGTCCCTGAAGGCCTCCAGACACAGGCGACCCCCAGCACTCACCTCCTCCAAGAAG CTTCCTACCTGTCCCTGAAGGCCTCCAGACACTGGCGACCCCCAGCACTCACCTCCTCCAAGAAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104874172..104874285 26863196 MeRIP-seq:(Medium) rs914166982 Functional Loss SNV dbSNP153 33..33 33 - - - 61249 RMVar_ID_61249 Human_SNP_ID_568507605 m1A Human chr14 - 104875517 104875517 104875517 TCCACACAGCGCTGCAAGCACGGCTGCTGCCCACCCGGCCTCCACTCCACACAGCACCCTGTGCT TCCACACAGCGCTGCAAGCACGGCTGCTGCCCGCCCGGCCTCCACTCCACACAGCACCCTGTGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104875511..104875648 26863196 MeRIP-seq:(Medium) rs1191224430 Functional Loss SNV dbSNP153 33..33 33 - - - 61250 RMVar_ID_61250 Human_SNP_ID_568510784 m1A Human chr14 - 104884487 104884487 104884487 CTCCGTGTCCTGCGCCTCGGTCTCGATGGTGTATGTCCCTGCGTCACTGAGGCTGTCGTCCTCCT CTCCGTGTCCTGCGCCTCGGTCTCGATGGTGTTTGTCCCTGCGTCACTGAGGCTGTCGTCCTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104884438..104884576 26863196 MeRIP-seq:(Medium) rs1174864228 Functional Loss SNV dbSNP153 33..33 33 - - - 61251 RMVar_ID_61251 Human_SNP_ID_568510796 m1A Human chr14 + 104884509 104884509 104884509 CGCAGGGACATACACCATCGAGACCGAGGCGCAGGACACGGAGGTGGAGGAGGCCCGGAAGATGA CGCAGGGACATACACCATCGAGACCGAGGCGCGGGACACGGAGGTGGAGGAGGCCCGGAAGATGA A G CEP170B Ensembl:ENSG00000099814 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104884458..104884574 26863196 MeRIP-seq:(Medium) rs768662962 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1560947,Human_Splice_Rec_1560977,Human_Splice_Rec_1561007 Human_miRNA_ID_208113,Human_miRNA_ID_2016479,Human_miRNA_ID_2465017 RMVar_hsa_circ_23318,RMVar_hsa_circ_103566,RMVar_hsa_circ_169669 61252 RMVar_ID_61252 Human_SNP_ID_568511883 m1A Human chr14 - 104886864 104886864 104886864 ATGTGGGGGGGCTTGCCGGGCGCTGGGGGACCACTGGCTGGCTCCTTAGTGAAGCTCTCTTGCCG ATGTGGGGGGGCTTGCCGGGCGCTGGGGGACCGCTGGCTGGCTCCTTAGTGAAGCTCTCTTGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104886820..104886960 26863196 MeRIP-seq:(Medium) rs550664070 Functional Loss SNV dbSNP153 33..33 33 - - - 61253 RMVar_ID_61253 Human_SNP_ID_568511884 m1A Human chr14 - 104886864 104886864 104886864 ATGTGGGGGGGCTTGCCGGGCGCTGGGGGACCACTGGCTGGCTCCTTAGTGAAGCTCTCTTGCCG ATGTGGGGGGGCTTGCCGGGCGCTGGGGGACCCCTGGCTGGCTCCTTAGTGAAGCTCTCTTGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104886820..104886960 26863196 MeRIP-seq:(Medium) rs550664070 Functional Loss SNV dbSNP153 33..33 33 - - - 61254 RMVar_ID_61254 Human_SNP_ID_568511910 m1A Human chr14 + 104886901 104886901 104886901 CCCCAGCGCCCGGCAAGCCCCCCCACATCTCCAGCCACCCGCTTCTACAGGACCTGGCCGCTACC CCCCAGCGCCCGGCAAGCCCCCCCACATCTCCGGCCACCCGCTTCTACAGGACCTGGCCGCTACC A G CEP170B Ensembl:ENSG00000099814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104886851..104886962 26863196 MeRIP-seq:(Medium) rs751517309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27429941 Human_miRNA_ID_1985085,Human_miRNA_ID_1985086,Human_miRNA_ID_2940723,Human_miRNA_ID_2940724 RMVar_hsa_circ_23318,RMVar_hsa_circ_103566,RMVar_hsa_circ_108473,RMVar_hsa_circ_169669,RMVar_hsa_circ_169670 61255 RMVar_ID_61255 Human_SNP_ID_568512166 m1A Human chr14 + 104887415 104887415 104887415 TGGCCCTGTCCTCGCCCACCTACCCAGCTCAGATGTGATGGCCTCCAACCACGAAACCCCTGAGG TGGCCCTGTCCTCGCCCACCTACCCAGCTCAGGTGTGATGGCCTCCAACCACGAAACCCCTGAGG A G CEP170B Ensembl:ENSG00000099814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104887364..104887479 26863196 MeRIP-seq:(Medium) rs754929468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2404212,Human_miRNA_ID_2404213 RMVar_hsa_circ_23318,RMVar_hsa_circ_103566,RMVar_hsa_circ_108473,RMVar_hsa_circ_169669,RMVar_hsa_circ_169670 61256 RMVar_ID_61256 Human_SNP_ID_568515143 m1A Human chr14 - 104895008 104895008 104895008 TGCGGCCAGGCAGGCGGGTGTGCGGCGGACGGAAGGCAGAGACGCACACGCACAGGGAGGCTGGC TGCGGCCAGGCAGGCGGGTGTGCGGCGGACGGTAGGCAGAGACGCACACGCACAGGGAGGCTGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104894957..104895205 26863196 MeRIP-seq:(Medium) rs1157188656 Functional Loss SNV dbSNP153 33..33 33 - - - 61257 RMVar_ID_61257 Human_SNP_ID_568515194 m1A Human chr14 - 104895146 104895141 104895146 CGAGGCAGGGGTGGGGGTGGCCATGGGGCTGGACAGGGTGAGTAGGGTGCTGGCTGGGAGCTGAC CGAGGCAGGGGTGGGGGTGGCCATGGGGCTGG_____GTGAGTAGGGTGCTGGCTGGGAGCTGAC CCCTGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104894964..104895248 26863196 MeRIP-seq:(Medium) rs1302639380 Functional Loss DEL dbSNP153 33..37 33 - - - 61258 RMVar_ID_61258 Human_SNP_ID_568515464 m1A Human chr14 - 104896173 104896173 104896173 CAGTGCCGCTCCCCCAGCAGCTGGCCCTGTCCAGGTCCGACTCTCATACCATTGCCAGGCAGGGT CAGTGCCGCTCCCCCAGCAGCTGGCCCTGTCCCGGTCCGACTCTCATACCATTGCCAGGCAGGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104896122..104896229 26863196 MeRIP-seq:(Medium) rs1163979810 Functional Loss SNV dbSNP153 33..33 33 - - - 61259 RMVar_ID_61259 Human_SNP_ID_568515582 m1A Human chr14 - 104896485 104896485 104896485 ACTGCCGAGGGGTGGGAAGGAGCCGTGGATGAAGCGTGACCACTTCATGTCCAGGGGCAGGCGGG ACTGCCGAGGGGTGGGAAGGAGCCGTGGATGAGGCGTGACCACTTCATGTCCAGGGGCAGGCGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104896449..104896545 26863196 MeRIP-seq:(Medium) rs931915551 Functional Loss SNV dbSNP153 33..33 33 - - - 61260 RMVar_ID_61260 Human_SNP_ID_568537421 m1A Human chr14 - 104953574 104953574 104953574 AGAGGCCACAGCAACAGCTGATAGAAGAGAACAGAGACGCACAGAGGAAGGATTAAAAGACAAAG AGAGGCCACAGCAACAGCTGATAGAAGAGAACTGAGACGCACAGAGGAAGGATTAAAAGACAAAG T A AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104953498..104954099 26863196 MeRIP-seq:(Medium) rs749694184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_122947,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 61261 RMVar_ID_61261 Human_SNP_ID_568537496 m1A Human chr14 + 104953753 104953753 104953753 TCTGTGTCTTCCCTGCCCTTGTCCTGTTCCTCAGTGATCCTTGTCCTCTGTAGTCCTTCCTCTCC TCTGTGTCTTCCCTGCCCTTGTCCTGTTCCTCCGTGATCCTTGTCCTCTGTAGTCCTTCCTCTCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104953449..104953953 26863196 MeRIP-seq:(Medium) rs756857966 Functional Loss SNV dbSNP153 33..33 33 - - - 61262 RMVar_ID_61262 Human_SNP_ID_568537770 m1A Human chr14 - 104954351 104954351 104954351 GGAAGAGTTGGGGCCCTGGGGTGATAGCCTCGAGGAGACTGGGGCTGCCACAGGCAGCAGGAGAG GGAAGAGTTGGGGCCCTGGGGTGATAGCCTCGGGGAGACTGGGGCTGCCACAGGCAGCAGGAGAG T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:104954181..104954704;chr14:104954166..104954666 26863196 MeRIP-seq:(Medium) rs1217730646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17845536 RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_122947,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 61263 RMVar_ID_61263 Human_SNP_ID_568537824 m1A Human chr14 - 104954466 104954466 104954466 AGAGGAGGCGGAAGTTCCTCAACCTCAGATTCAGGACAGGCTCGGGACAGGGCCCTTCATCGACA AGAGGAGGCGGAAGTTCCTCAACCTCAGATTCGGGACAGGCTCGGGACAGGGCCCTTCATCGACA T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:104954451..104954475 26863196 MeRIP-seq:(Medium) rs1299149697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8400573 Human_miRNA_ID_2225483,Human_miRNA_ID_2444262,Human_miRNA_ID_2937536 RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_122947,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 61264 RMVar_ID_61264 Human_SNP_ID_568537840 m1A Human chr14 - 104954512 104954512 104954512 CAGCTCACGGTGGAGCGCCAAGAGCAGAAGGCAGGGCCGGGCAGCCAGAGGAGGCGGAAGTTCCT CAGCTCACGGTGGAGCGCCAAGAGCAGAAGGCGGGGCCGGGCAGCCAGAGGAGGCGGAAGTTCCT T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:104954402..104954600 26863196 MeRIP-seq:(Medium) rs1265118683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_122947,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 61265 RMVar_ID_61265 Human_SNP_ID_568540962 m1A Human chr14 + 104966263 104966263 104966263 CACCTTCCTACTGCTCCGGGGGCCAGGCCCAGACCCCTGGCCTCCATAACCCCCCAGCAGAGCCA CACCTTCCTACTGCTCCGGGGGCCAGGCCCAGCCCCCTGGCCTCCATAACCCCCCAGCAGAGCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104966256..104966625 26863196 MeRIP-seq:(Medium) rs1057153172 Functional Loss SNV dbSNP153 33..33 33 - - - 61266 RMVar_ID_61266 Human_SNP_ID_568542047 m1A Human chr14 - 104970388 104970365 104970389 TTGCCTCACTCTTCCGCGGGTCTGTGGGGGCCAGCAGGCCACCAGCAAGGGGGGCTGGAGGAACA TTGCCTCACTCTTCCGCGGGTCTGTGGGGGC________________________TGGAGGAACA AGCCCCCCTTGCTGGTGGCCTGCTG A AHNAK2 Ensembl:ENSG00000185567 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104970384..104970681 26863196 MeRIP-seq:(Medium) rs981393634 Functional Loss DEL dbSNP153 32..55 33 - - - RMVar_hsa_circ_77373,RMVar_hsa_circ_113263,RMVar_hsa_circ_169680,RMVar_hsa_circ_169679 61267 RMVar_ID_61267 Human_SNP_ID_568546270 m1A Human chr14 + 104985865 104985862 104985866 TTCTCTCGCCCTGGTCCCGCGCGGCCCCGCCGAGGCGGCGACCAAGGTGGGTGCGGGGACTCTCG TTCTCTCGCCCTGGTCCCGCGCGGCCCCGC____GCGGCGACCAAGGTGGGTGCGGGGACTCTCG CCGAG C CLBA1 Ensembl:ENSG00000140104 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104985829..104985939 26863196 MeRIP-seq:(Medium) rs1201294919 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4284768 Human_Splice_Rec_1561145,Human_Splice_Rec_1561161 61268 RMVar_ID_61268 Human_SNP_ID_568548308 m1A Human chr14 + 104992028 104992004 104992028 CACACACCTCACGCCACCACATGCCGCCATGCACACGCCGCCACGCACACGCCACCACGCACACG CACACACCT________________________CACGCCGCCACGCACACGCCACCACGCACACG TCACGCCACCACATGCCGCCATGCA T CLBA1 Ensembl:ENSG00000140104 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104991979..104992132 26863196 MeRIP-seq:(Medium) rs1566933338 Functional Loss DEL dbSNP153 10..33 33 - - - 61269 RMVar_ID_61269 Human_SNP_ID_568548324 m1A Human chr14 + 104992028 104992026 104992028 CACACACCTCACGCCACCACATGCCGCCATGCACACGCCGCCACGCACACGCCACCACGCACACG CACACACCTCACGCCACCACATGCCGCCATG__CACGCCGCCACGCACACGCCACCACGCACACG GCA G CLBA1 Ensembl:ENSG00000140104 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104991979..104992132 26863196 MeRIP-seq:(Medium) rs1268310143 Functional Loss DEL dbSNP153 32..33 33 - - - 61270 RMVar_ID_61270 Human_SNP_ID_568548391 m1A Human chr14 + 104992124 104992110 104992124 CACACACCACCACATGCCGCCATGCACACGCCACCACGCACACGCCGCCATGCACACGCCTCACA CACACACCACCACATGCCG______________CCACGCACACGCCGCCATGCACACGCCTCACA GCCATGCACACGCCA G CLBA1 Ensembl:ENSG00000140104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104991906..104992300 26863196 MeRIP-seq:(Medium) rs1169838814 Functional Loss DEL dbSNP153 20..33 33 - - - 61271 RMVar_ID_61271 Human_SNP_ID_568548393 m1A Human chr14 + 104992113 104992113 104992113 CGCACATGCCTCACACACCACCACATGCCGCCATGCACACGCCACCACGCACACGCCGCCATGCA CGCACATGCCTCACACACCACCACATGCCGCCTTGCACACGCCACCACGCACACGCCGCCATGCA A T CLBA1 Ensembl:ENSG00000140104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104991861..104992325 26863196 MeRIP-seq:(Medium) rs1237730963 Functional Loss SNV dbSNP153 33..33 33 - - - 61272 RMVar_ID_61272 Human_SNP_ID_568548401 m1A Human chr14 + 104992124 104992124 104992124 CACACACCACCACATGCCGCCATGCACACGCCACCACGCACACGCCGCCATGCACACGCCTCACA CACACACCACCACATGCCGCCATGCACACGCCGCCACGCACACGCCGCCATGCACACGCCTCACA A G CLBA1 Ensembl:ENSG00000140104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104991906..104992300 26863196 MeRIP-seq:(Medium) rs1483873205 Functional Loss SNV dbSNP153 33..33 33 - - - 61273 RMVar_ID_61273 Human_SNP_ID_96847705 m1A Human chr2 + 150486518 150486518 150486518 GCTCTCCTCTCCCCACTGCTATCTCCTCGTCCACGCTGTCGTCTGCCGCCCCCACCCAGAAGGGA GCTCTCCTCTCCCCACTGCTATCTCCTCGTCCGCGCTGTCGTCTGCCGCCCCCACCCAGAAGGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:150486510..150486619 32194978 MeRIP-seq:(Medium) rs1018837982 Functional Loss SNV dbSNP153 33..33 33 - - - 61274 RMVar_ID_61274 Human_SNP_ID_97035751 m1A Human chr2 + 151289546 151289546 151289546 CTCCCTTTCCACCCCCGGCTCTCCAGCCCGGGACTGCCAGCGGCGGGAGTGGCAGCCGGGGAAGG CTCCCTTTCCACCCCCGGCTCTCCAGCCCGGGGCTGCCAGCGGCGGGAGTGGCAGCCGGGGAAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:151289538..151289646 26863196 MeRIP-seq:(Medium) rs1286834457 Functional Loss SNV dbSNP153 33..33 33 - - - 61275 RMVar_ID_61275 Human_SNP_ID_97065664 m1A Human chr2 - 151410031 151410031 151410031 CTACCACTGTCACCCCGATATTTATCCCACCTAGGAAGATCAGGACAGGGTTCTCTCCGCCTCTG CTACCACTGTCACCCCGATATTTATCCCACCTGGGAAGATCAGGACAGGGTTCTCTCCGCCTCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:151410011..151410111 32194978 MeRIP-seq:(Medium) rs1211036066 Functional Loss SNV dbSNP153 33..33 33 - - - 61276 RMVar_ID_61276 Human_SNP_ID_97065759 m1A Human chr2 + 151410247 151410247 151410247 CGTGGGCTCAGGTGTCTGGTGTCGGGCGCCGGAGGAGGTTCGCGCTGGGGTTTGGTGATTCGGAG CGTGGGCTCAGGTGTCTGGTGTCGGGCGCCGGTGGAGGTTCGCGCTGGGGTTTGGTGATTCGGAG A T RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:151410196..151410345 26863196 MeRIP-seq:(Medium) rs1360128143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243405,Human_RBP_ID_916631,Human_RBP_ID_4622715,Human_RBP_ID_5147173,Human_RBP_ID_5381684,Human_RBP_ID_8851568,Human_RBP_ID_9353917,Human_RBP_ID_17135920 61277 RMVar_ID_61277 Human_SNP_ID_97065764 m1A Human chr2 - 151410265 151410265 151410265 CGCGTCTGCACCCCAGGCCTCCGAATCACCAAACCCCAGCGCGAACCTCCTCCGGCGCCCGACAC CGCGTCTGCACCCCAGGCCTCCGAATCACCAAGCCCCAGCGCGAACCTCCTCCGGCGCCCGACAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:151410214..151410327 26863196 MeRIP-seq:(Medium) rs998833322 Functional Loss SNV dbSNP153 33..33 33 - - - 61278 RMVar_ID_61278 Human_SNP_ID_97169180 m1A Human chr2 - 151828200 151828200 151828200 GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGAGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGTGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT T A ARL5A,AC068547.1 Ensembl:ENSG00000162980,Ensembl:ENSG00000283228 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:151828151..151828350 32194978 MeRIP-seq:(Medium) rs201916854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_535742,Human_RBP_ID_777294,Human_RBP_ID_4622717,Human_RBP_ID_9331192,Human_RBP_ID_17392807 Human_Splice_Rec_308451,Human_Splice_Rec_308479 61279 RMVar_ID_61279 Human_SNP_ID_97169181 m1A Human chr2 - 151828200 151828200 151828200 GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGAGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGGGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT T C ARL5A,AC068547.1 Ensembl:ENSG00000162980,Ensembl:ENSG00000283228 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:151828151..151828350 32194978 MeRIP-seq:(Medium) rs201916854 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_535742,Human_RBP_ID_777294,Human_RBP_ID_4622717,Human_RBP_ID_9331192,Human_RBP_ID_17392807 Human_Splice_Rec_308451,Human_Splice_Rec_308479 61280 RMVar_ID_61280 Human_SNP_ID_97169229 m1A Human chr2 + 151828317 151828317 151828317 CTCCCGCGCTGGTCGCGGGCCCGCTTCCAGGGAACCGGAGGGAGGCCGAAGCCCAGGCCGCCCTG CTCCCGCGCTGGTCGCGGGCCCGCTTCCAGGGTACCGGAGGGAGGCCGAAGCCCAGGCCGCCCTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:151828268..151828442 26863196 MeRIP-seq:(Medium) rs930889344 Functional Loss SNV dbSNP153 33..33 33 - - - 61281 RMVar_ID_61281 Human_SNP_ID_97169244 m1A Human chr2 - 151828348 151828348 151828348 CGCGGCGGCAGCGGCGGGGCCTTGCGCGCGGCAGGGCGGCCTGGGCTTCGGCCTCCCTCCGGTTC CGCGGCGGCAGCGGCGGGGCCTTGCGCGCGGCCGGGCGGCCTGGGCTTCGGCCTCCCTCCGGTTC T G ARL5A,AC068547.1 Ensembl:ENSG00000162980,Ensembl:ENSG00000283228 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr2:151828260..151828424;chr2:151828299..151828441 26863410,26863196 MeRIP-seq:(Medium) rs1355719972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243838,Human_RBP_ID_777295,Human_RBP_ID_4622718,Human_RBP_ID_5239882,Human_RBP_ID_9330693,Human_RBP_ID_22451626 61282 RMVar_ID_61282 Human_SNP_ID_97251323 m1A Human chr2 + 152175540 152175540 152175540 CTAGTCCCCGGAGTCGCTACCGCCCACTTTCTAGCCGGACAAACAGCAGTCCAGGGCCAGGCACA CTAGTCCCCGGAGTCGCTACCGCCCACTTTCTTGCCGGACAAACAGCAGTCCAGGGCCAGGCACA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:152175536..152175638 32194978 MeRIP-seq:(Medium) rs1280259507 Functional Loss SNV dbSNP153 33..33 33 - - - 61283 RMVar_ID_61283 Human_SNP_ID_97251419 m1A Human chr2 + 152175710 152175710 152175710 GCTGACACTCAGCAACTGCTACCCGCCGGGTGACCCGCGGCCGCGGCTCCCTAGACCGCTCCGCT GCTGACACTCAGCAACTGCTACCCGCCGGGTGGCCCGCGGCCGCGGCTCCCTAGACCGCTCCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:152175567..152175909;chr2:152150171..152175906;chr2:152150171..152175899 26863196 MeRIP-seq:(Medium) rs1280310927 Functional Loss SNV dbSNP153 33..33 33 - - - 61284 RMVar_ID_61284 Human_SNP_ID_97288069 m1A Human chr2 + 152335170 152335170 152335170 AGGTGGCATTGTGTAGGGGAGCGCGGAGCTGCATTTGTCTGCTCCAGGTGCTAGCCAGGCAGGCG AGGTGGCATTGTGTAGGGGAGCGCGGAGCTGCCTTTGTCTGCTCCAGGTGCTAGCCAGGCAGGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:152335121..152335635 26863196 MeRIP-seq:(Medium) rs576315369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4583764,Human_RBP_ID_22244064 61285 RMVar_ID_61285 Human_SNP_ID_97288070 m1A Human chr2 + 152335170 152335170 152335170 AGGTGGCATTGTGTAGGGGAGCGCGGAGCTGCATTTGTCTGCTCCAGGTGCTAGCCAGGCAGGCG AGGTGGCATTGTGTAGGGGAGCGCGGAGCTGCGTTTGTCTGCTCCAGGTGCTAGCCAGGCAGGCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:152335121..152335635 26863196 MeRIP-seq:(Medium) rs576315369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4583764,Human_RBP_ID_22244064 61286 RMVar_ID_61286 Human_SNP_ID_97288122 m1A Human chr2 - 152335294 152335294 152335294 GTGCTCCGCTGGCACACCGCCCCCTGCCAGAGATCGCGGCCCCCGGCGCGTGGTCCCTCCTACTC GTGCTCCGCTGGCACACCGCCCCCTGCCAGAGGTCGCGGCCCCCGGCGCGTGGTCCCTCCTACTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:152335244..152335399 32194978 MeRIP-seq:(Medium) rs966649118 Functional Loss SNV dbSNP153 33..33 33 - - - 61287 RMVar_ID_61287 Human_SNP_ID_97291882 m1A Human chr2 - 152350037 152350037 152350037 ACGCTCCATTTCTGTACCTGTGCATCCCCTTCAGGTCTGGCTTCCCCCTCTACGCCCTCCCATTA ACGCTCCATTTCTGTACCTGTGCATCCCCTTCGGGTCTGGCTTCCCCCTCTACGCCCTCCCATTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:152350026..152350145 26863196 MeRIP-seq:(Medium) rs1006515248 Functional Loss SNV dbSNP153 33..33 33 - - - 61288 RMVar_ID_61288 Human_SNP_ID_97295693 m1A Human chr2 + 152365237 152365237 152365237 CTTAAGGAGAGTTGACTTGAATTGGAGAGTGGAAGATGAATGTAATGGCTTGGAATTGAGGAGAG CTTAAGGAGAGTTGACTTGAATTGGAGAGTGGTAGATGAATGTAATGGCTTGGAATTGAGGAGAG A T FMNL2 Ensembl:ENSG00000157827 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:152365232..152365329 26863196 MeRIP-seq:(Medium) rs1313067484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23830227 61289 RMVar_ID_61289 Human_SNP_ID_97303684 m1A Human chr2 - 152399857 152399846 152399857 TTTTGCTCAGCACTCTTCATCCAGTAGCTAGCACTCCACCTGCCACATAGAACTCACCCAAATAT TTTTGCTCAGCACTCTTCATCCAGTAGCTAGC___________CACATAGAACTCACCCAAATAT GGCAGGTGGAGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:152399848..152399932 26863196 MeRIP-seq:(Medium) rs910709714 Functional Loss DEL dbSNP153 33..43 33 - - - 61290 RMVar_ID_61290 Human_SNP_ID_97368033 m1A Human chr2 + 152672521 152672521 152672521 TGATTTTCAAGAAAACGCTGAAAGGATTCCTTAGCCTCTTTGTACTTTGATCTTGCTTCTTCTTT TGATTTTCAAGAAAACGCTGAAAGGATTCCTTGGCCTCTTTGTACTTTGATCTTGCTTCTTCTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:152672470..152672621 32194978 MeRIP-seq:(Medium) rs766851506 Functional Loss SNV dbSNP153 33..33 33 - - - 61291 RMVar_ID_61291 Human_SNP_ID_97369257 m1A Human chr2 + 152676678 152676678 152676678 CTGCTGCTGCTGCCGCTGCTGCTGCTGCAACAACAGCAGCTGCTGCTTCGGCAGCAGCCATGGTG CTGCTGCTGCTGCCGCTGCTGCTGCTGCAACAGCAGCAGCTGCTGCTTCGGCAGCAGCCATGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:152673629..152679072 32194978 MeRIP-seq:(Medium) rs547638795 Functional Loss SNV dbSNP153 33..33 33 - - - 61292 RMVar_ID_61292 Human_SNP_ID_97380256 m1A Human chr2 + 152717374 152717374 152717374 TCCATTTCACTCACCATGAGGCCTCCACGCTCAGCTCCCGTCCCCGGCCTCATCGTCGGGCTCAG TCCATTTCACTCACCATGAGGCCTCCACGCTCCGCTCCCGTCCCCGGCCTCATCGTCGGGCTCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:152717192..152717425;chr2:152717175..152717425 26863196 MeRIP-seq:(Medium) rs757611982 Functional Loss SNV dbSNP153 33..33 33 - - - 61293 RMVar_ID_61293 Human_SNP_ID_97380257 m1A Human chr2 + 152717374 152717374 152717374 TCCATTTCACTCACCATGAGGCCTCCACGCTCAGCTCCCGTCCCCGGCCTCATCGTCGGGCTCAG TCCATTTCACTCACCATGAGGCCTCCACGCTCGGCTCCCGTCCCCGGCCTCATCGTCGGGCTCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:152717192..152717425;chr2:152717175..152717425 26863196 MeRIP-seq:(Medium) rs757611982 Functional Loss SNV dbSNP153 33..33 33 - - - 61294 RMVar_ID_61294 Human_SNP_ID_97507710 m1A Human chr2 - 153222345 153222343 153222345 AAGTACTTCCTCCCTTCTAAGCCTATAAGCCCAACCCCCCCCCCCACCCCACCCCCCCCCCCCCC AAGTACTTCCTCCCTTCTAAGCCTATAAGCCC__CCCCCCCCCCCACCCCACCCCCCCCCCCCCC GTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:153222301..153222350 26863196 MeRIP-seq:(Medium) rs1558843433 Functional Loss DEL dbSNP153 33..34 33 - - - 61295 RMVar_ID_61295 Human_SNP_ID_97507713 m1A Human chr2 - 153222345 153222345 153222345 AAGTACTTCCTCCCTTCTAAGCCTATAAGCCCAACCCCCCCCCCCACCCCACCCCCCCCCCCCCC AAGTACTTCCTCCCTTCTAAGCCTATAAGCCCCACCCCCCCCCCCACCCCACCCCCCCCCCCCCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:153222301..153222350 26863196 MeRIP-seq:(Medium) rs1385138841 Functional Loss SNV dbSNP153 33..33 33 - - - 61296 RMVar_ID_61296 Human_SNP_ID_97706356 m1A Human chr2 - 154018831 154018831 154018831 GTCTCTCCTCCTCCTCCTCTCTCATCCTTTCTACCATCTTCCATCTCACTCTCCTTCATCCCCGT GTCTCTCCTCCTCCTCCTCTCTCATCCTTTCTTCCATCTTCCATCTCACTCTCCTTCATCCCCGT T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:154018739..154018912 26863196 MeRIP-seq:(Medium) rs1558911025 Functional Loss SNV dbSNP153 33..33 33 - - - 61297 RMVar_ID_61297 Human_SNP_ID_98261330 m1A Human chr2 - 156326572 156326569 156326573 AATGGAAGTCGGAGAAAGGAAGAAAAAGAAAGAAAACAAAAAAAGACGAGAAGAAGCGAGCCCAG AATGGAAGTCGGAGAAAGGAAGAAAAAGAAA____ACAAAAAAAGACGAGAAGAAGCGAGCCCAG TTTTC T NR4A2 Ensembl:ENSG00000153234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:156326522..156326663 26863196 MeRIP-seq:(Medium) rs1248193078 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_19188 61298 RMVar_ID_61298 Human_SNP_ID_98262990 m1A Human chr2 + 156332584 156332584 156332584 CCGGGGTCGGGTAGGGGTGGGAGAGCTGGGCGAAGGGAACCCGGACACCTCACGGAGGGAGGGAG CCGGGGTCGGGTAGGGGTGGGAGAGCTGGGCGGAGGGAACCCGGACACCTCACGGAGGGAGGGAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:156332468..156332705 26863196 MeRIP-seq:(Medium) rs1852536 Functional Loss SNV dbSNP153 33..33 33 - - - 61299 RMVar_ID_61299 Human_SNP_ID_98263012 m1A Human chr2 - 156332663 156332663 156332663 CGGCCAGGGCCAGTCCGCCCGGCGGCTCGCGCACGGCTCCGCGGTCCCTTTTGCCTGTCCAGCCG CGGCCAGGGCCAGTCCGCCCGGCGGCTCGCGCGCGGCTCCGCGGTCCCTTTTGCCTGTCCAGCCG T C NR4A2 Ensembl:ENSG00000153234 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:156332476..156332700;chr2:156332484..156332693;chr2:156332490..156332687 26863196 MeRIP-seq:(Medium) rs544647039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22504602 61300 RMVar_ID_61300 Human_SNP_ID_98280052 m1A Human chr2 + 156400825 156400825 156400825 GCGCGCTTCGCATGTGTGAGGTCCCGGGTTCAATCCCCGGCATCTCCAAATCAGCCGACGTTTGC GCGCGCTTCGCATGTGTGAGGTCCCGGGTTCAGTCCCCGGCATCTCCAAATCAGCCGACGTTTGC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1269437052 Functional Loss SNV dbSNP153 33..33 33 - - - 61301 RMVar_ID_61301 Human_SNP_ID_98288003 m1A Human chr2 - 156435713 156435713 156435713 CGGCAGGCTTCCCTAGGCCTACAGACGTGTCCAGGAGGCGGGCGACCCTGCGACCCCGCCGTCAG CGGCAGGCTTCCCTAGGCCTACAGACGTGTCCCGGAGGCGGGCGACCCTGCGACCCCGCCGTCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:156435663..156435761;chr2:156435664..156435778;chr2:156435628..156435781 26863196 MeRIP-seq:(Medium) rs1430193528 Functional Loss SNV dbSNP153 33..33 33 - - - 61302 RMVar_ID_61302 Human_SNP_ID_98288154 m1A Human chr2 + 156436231 156436231 156436231 TTTCCCCGCTGGGCCGGAGGAGCCTGGGCCCGAGGTATCCGGGCAGGAGGTGGCGGCCTCGCCGC TTTCCCCGCTGGGCCGGAGGAGCCTGGGCCCGCGGTATCCGGGCAGGAGGTGGCGGCCTCGCCGC A C GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:156436220..156436339 26863196 MeRIP-seq:(Medium) rs1439572076 Functional Loss SNV dbSNP153 33..33 33 - - - 61303 RMVar_ID_61303 Human_SNP_ID_98292227 m1A Human chr2 + 156452612 156452612 156452612 GAGAACTCTTTCAAGAAGTTTCATTATGAAGGAAAGCAGAGACGTGGAAAAGTTCTTGGAAGAGG GAGAACTCTTTCAAGAAGTTTCATTATGAAGGTAAGCAGAGACGTGGAAAAGTTCTTGGAAGAGG A T GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:156452605..156452845 26863196 MeRIP-seq:(Medium) rs1283587625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23831758 61304 RMVar_ID_61304 Human_SNP_ID_98292245 m1A Human chr2 - 156452664 156452664 156452664 GAAATTCACTGTATTATCCTCTAGTTCTAACAAACCCTCCCTTGACCAATATCCTCTTCCAAGAA GAAATTCACTGTATTATCCTCTAGTTCTAACACACCCTCCCTTGACCAATATCCTCTTCCAAGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:156452663..156452860 26863196 MeRIP-seq:(Medium) rs534034436 Functional Loss SNV dbSNP153 33..33 33 - - - 61305 RMVar_ID_61305 Human_SNP_ID_98292433 m1A Human chr2 + 156453435 156453435 156453435 TCCAGACTACAGTAGATAAACTGAAGAAAGAGAAGGTGGTGTTTACAGTGTAGGGTGCTTGAGGC TCCAGACTACAGTAGATAAACTGAAGAAAGAGGAGGTGGTGTTTACAGTGTAGGGTGCTTGAGGC A G GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:156453432..156453576 26863196 MeRIP-seq:(Medium) rs1257951129 Functional Loss SNV dbSNP153 33..33 33 - - - 61306 RMVar_ID_61306 Human_SNP_ID_98292559 m1A Human chr2 + 156453911 156453911 156453911 AAACAAAAAACAAAACAAAAAAGAAAACTGCAATGATGAAGACAGATGAGTCTGGAAAGGGAAAT AAACAAAAAACAAAACAAAAAAGAAAACTGCAGTGATGAAGACAGATGAGTCTGGAAAGGGAAAT A G GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:156453905..156454074 26863196 MeRIP-seq:(Medium) rs1224682299 Functional Loss SNV dbSNP153 33..33 33 - - - 61307 RMVar_ID_61307 Human_SNP_ID_98292562 m1A Human chr2 + 156453920 156453920 156453920 ACAAAACAAAAAAGAAAACTGCAATGATGAAGACAGATGAGTCTGGAAAGGGAAATAGGTATGAA ACAAAACAAAAAAGAAAACTGCAATGATGAAGGCAGATGAGTCTGGAAAGGGAAATAGGTATGAA A G GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:156453918..156454013 26863196 MeRIP-seq:(Medium) rs755571823 Functional Loss SNV dbSNP153 33..33 33 - - - 61308 RMVar_ID_61308 Human_SNP_ID_98293180 m1A Human chr2 + 156456812 156456812 156456812 GGGGAGGGTGAAGGTGGGTTGGGGGCTGTGGGAGAGTCTGAGCAATAAGGAGATGGCGTAGCATG GGGGAGGGTGAAGGTGGGTTGGGGGCTGTGGGCGAGTCTGAGCAATAAGGAGATGGCGTAGCATG A C GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:156456809..156456892 26863196 MeRIP-seq:(Medium) rs1266665423 Functional Loss SNV dbSNP153 33..33 33 - - - 61309 RMVar_ID_61309 Human_SNP_ID_98310681 m1A Human chr2 - 156535026 156535026 156535026 CCTGTAATTCCATGGGTCTGCATGCTTTGGCCACAGTGTTCCCTGTCATCTTCCTCCCCCACTGA CCTGTAATTCCATGGGTCTGCATGCTTTGGCCTCAGTGTTCCCTGTCATCTTCCTCCCCCACTGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:156535015..156535087 26863196 MeRIP-seq:(Medium) rs969354233 Functional Loss SNV dbSNP153 33..33 33 - - - 61310 RMVar_ID_61310 Human_SNP_ID_98310723 m1A Human chr2 - 156535254 156535254 156535254 TCTCTCTCTCTCACCTGGGATTCCTTCCCATCAGCATAAAATCTCATCTAATGCCCTCCTATTAA TCTCTCTCTCTCACCTGGGATTCCTTCCCATCTGCATAAAATCTCATCTAATGCCCTCCTATTAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:156535208..156535382 26863196 MeRIP-seq:(Medium) rs1330913433 Functional Loss SNV dbSNP153 33..33 33 - - - 61311 RMVar_ID_61311 Human_SNP_ID_98620486 m1A Human chr2 - 157875903 157875903 157875903 CCCGCAGAGTTCCGGGCTCCCTCGCCGGCTGCACCGCCCCGCCCCGCCCCGCGCCGCCCCGCGCC CCCGCAGAGTTCCGGGCTCCCTCGCCGGCTGCCCCGCCCCGCCCCGCCCCGCGCCGCCCCGCGCC T G ACVR1 Ensembl:ENSG00000115170 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:157875770..157876079 26863196 MeRIP-seq:(Medium) rs1278498478 Functional Loss SNV dbSNP153 33..33 33 - - - 61312 RMVar_ID_61312 Human_SNP_ID_98620488 m1A Human chr2 + 157875906 157875906 157875906 GCGGGGCGGCGCGGGGCGGGGCGGGGCGGTGCAGCCGGCGAGGGAGCCCGGAACTCTGCGGGGCC GCGGGGCGGCGCGGGGCGGGGCGGGGCGGTGCGGCCGGCGAGGGAGCCCGGAACTCTGCGGGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:157875860..157876071 26863196 MeRIP-seq:(Medium) rs1337166464 Functional Loss SNV dbSNP153 33..33 33 - - - 61313 RMVar_ID_61313 Human_SNP_ID_98620611 m1A Human chr2 - 157876234 157876234 157876234 CTGTGACGGTCTCCCCCGCCGCCCCCGGGGGCAAGCCCAGCTGGTCCGCCCGCCCCGCCCGCGGT CTGTGACGGTCTCCCCCGCCGCCCCCGGGGGCCAGCCCAGCTGGTCCGCCCGCCCCGCCCGCGGT T G ACVR1 Ensembl:ENSG00000115170 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:157876147..157876238 26863410 MeRIP-seq:(Medium) rs1230514256 Functional Loss SNV dbSNP153 33..33 33 - - - 61314 RMVar_ID_61314 Human_SNP_ID_98762193 m1A Human chr2 + 158457094 158457093 158457094 AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGGAGGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGG_GGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC GA G PKP4 Ensembl:ENSG00000144283 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:158456970..158457099 26863196 MeRIP-seq:(Medium) rs1229533163 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3638184,Human_RBP_ID_4622725,Human_RBP_ID_5239673,Human_RBP_ID_5322655,Human_RBP_ID_5381702,Human_RBP_ID_8200720,Human_RBP_ID_8728732,Human_RBP_ID_9330702,Human_RBP_ID_9428843,Human_RBP_ID_18948334,Human_RBP_ID_20615816,Human_RBP_ID_22596441,Human_RBP_ID_24553139,Human_RBP_ID_26787214 61315 RMVar_ID_61315 Human_SNP_ID_98762194 m1A Human chr2 + 158457094 158457094 158457094 AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGGAGGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGGGGGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC A G PKP4 Ensembl:ENSG00000144283 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:158456970..158457099 26863196 MeRIP-seq:(Medium) rs976473870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638184,Human_RBP_ID_4622725,Human_RBP_ID_5239673,Human_RBP_ID_5322655,Human_RBP_ID_5381702,Human_RBP_ID_8200720,Human_RBP_ID_8728732,Human_RBP_ID_9330702,Human_RBP_ID_9428843,Human_RBP_ID_18948334,Human_RBP_ID_20615816,Human_RBP_ID_22596441,Human_RBP_ID_24553139,Human_RBP_ID_26787214 61316 RMVar_ID_61316 Human_SNP_ID_98762214 m1A Human chr2 + 158457151 158457151 158457151 CGCGGCACTTTTTTAATTTTTTCGGGTGCCGCAGCGGCGACCCCTCGGCGCCGATGTCCCTGATC CGCGGCACTTTTTTAATTTTTTCGGGTGCCGCTGCGGCGACCCCTCGGCGCCGATGTCCCTGATC A T PKP4 Ensembl:ENSG00000144283 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:158456974..158457175 26863196 MeRIP-seq:(Medium) rs1339739631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243764,Human_RBP_ID_3641059,Human_RBP_ID_4624796,Human_RBP_ID_5239673,Human_RBP_ID_5322222,Human_RBP_ID_8201699,Human_RBP_ID_9330703,Human_RBP_ID_9428844,Human_RBP_ID_18193394,Human_RBP_ID_18948335,Human_RBP_ID_22743025,Human_RBP_ID_22997466,Human_RBP_ID_24422424,Human_RBP_ID_26786332 Human_Splice_Rec_311771,Human_Splice_Rec_311809,Human_Splice_Rec_311847,Human_Splice_Rec_311883,Human_Splice_Rec_311921,Human_Splice_Rec_311931,Human_Splice_Rec_311933,Human_Splice_Rec_311955 61317 RMVar_ID_61317 Human_SNP_ID_98762240 m1A Human chr2 - 158457204 158457204 158457204 GCGAGCCCACACACTTACTTTCCAGCTTAGGCAGCGGCCGTCGTCGCTCCAGGGATCAGGGACAT GCGAGCCCACACACTTACTTTCCAGCTTAGGCGGCGGCCGTCGTCGCTCCAGGGATCAGGGACAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:158457127..158458295 26863196 MeRIP-seq:(Medium) rs1280478661 Functional Loss SNV dbSNP153 33..33 33 - - - 61318 RMVar_ID_61318 Human_SNP_ID_98762472 m1A Human chr2 - 158457724 158457724 158457724 CAAGACCGCGCGGGCAGCAGGGGCGTGGGAAGACGGGGAGGGGACCAAGGTGCAGGATCTGGGGC CAAGACCGCGCGGGCAGCAGGGGCGTGGGAAGCCGGGGAGGGGACCAAGGTGCAGGATCTGGGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:158457719..158457893 26863196 MeRIP-seq:(Medium) rs887773131 Functional Loss SNV dbSNP153 33..33 33 - - - 61319 RMVar_ID_61319 Human_SNP_ID_98762483 m1A Human chr2 - 158457752 158457752 158457752 AAGGAGTACAGGACTTCGGGGACAAACGCAAGACCGCGCGGGCAGCAGGGGCGTGGGAAGACGGG AAGGAGTACAGGACTTCGGGGACAAACGCAAGTCCGCGCGGGCAGCAGGGGCGTGGGAAGACGGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:158457721..158457917 26863196 MeRIP-seq:(Medium) rs752067655 Functional Loss SNV dbSNP153 33..33 33 - - - 61320 RMVar_ID_61320 Human_SNP_ID_98762647 m1A Human chr2 + 158458179 158458179 158458179 GGGGACGCGCGCTGCCGGCTCCTGGGCTGGCGACAGATTGTGCAGGAATGCGAGGAATGCACCAG GGGGACGCGCGCTGCCGGCTCCTGGGCTGGCGGCAGATTGTGCAGGAATGCGAGGAATGCACCAG A G PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:158458177..158458279 26863196 MeRIP-seq:(Medium) rs952535649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264425,Human_RBP_ID_5131652,Human_RBP_ID_5239888,Human_RBP_ID_5322657,Human_RBP_ID_8109962,Human_RBP_ID_18462224,Human_RBP_ID_18493612,Human_RBP_ID_22417200,Human_RBP_ID_22449997,Human_RBP_ID_22548533,Human_RBP_ID_22699704,Human_RBP_ID_22720750,Human_RBP_ID_22742786,Human_RBP_ID_26787218 RMVar_hsa_circ_203985,RMVar_hsa_circ_76123 61321 RMVar_ID_61321 Human_SNP_ID_98774253 m1A Human chr2 - 158505651 158505651 158505651 TTCCCTGCCACTCCAAAACCCTCACTTCTCCTATCACCCACCCTGCTTCTTTTCTCACCTTAATG TTCCCTGCCACTCCAAAACCCTCACTTCTCCTGTCACCCACCCTGCTTCTTTTCTCACCTTAATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:158505645..158505767 26863196 MeRIP-seq:(Medium) rs1304398418 Functional Loss SNV dbSNP153 33..33 33 - - - 61322 RMVar_ID_61322 Human_SNP_ID_98781815 m1A Human chr2 + 158533240 158533240 158533240 ATTGGTGGAGGAGGGGCAACCACAGACCCGCCAGGAAGCTGCCTCCACTGGCCCAGGCATGGAAC ATTGGTGGAGGAGGGGCAACCACAGACCCGCCGGGAAGCTGCCTCCACTGGCCCAGGCATGGAAC A G PKP4 Ensembl:ENSG00000144283 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:158533155..158533300 26863196 MeRIP-seq:(Medium) rs780810544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_536321,Human_RBP_ID_922194,Human_RBP_ID_4584514,Human_RBP_ID_9387542 Human_Splice_Rec_311772,Human_Splice_Rec_311773,Human_Splice_Rec_311810,Human_Splice_Rec_311811,Human_Splice_Rec_311848,Human_Splice_Rec_311849,Human_Splice_Rec_311884,Human_Splice_Rec_311885,Human_Splice_Rec_311922,Human_Splice_Rec_311923,Human_Splice_Rec_311934,Human_Splice_Rec_311935,Human_Splice_Rec_311956,Human_Splice_Rec_311957,Human_Splice_Rec_311966,Human_Splice_Rec_311967,Human_Splice_Rec_311997 RMVar_hsa_circ_93424,RMVar_hsa_circ_287107,RMVar_hsa_circ_323109,RMVar_hsa_circ_203985,RMVar_hsa_circ_76123,RMVar_hsa_circ_203986,RMVar_hsa_circ_332421,RMVar_hsa_circ_292372,RMVar_hsa_circ_305195,RMVar_hsa_circ_290563,RMVar_hsa_circ_115220,RMVar_hsa_circ_279386,RMVar_hsa_circ_107361,RMVar_hsa_circ_203990,RMVar_hsa_circ_203992,RMVar_hsa_circ_203994,RMVar_hsa_circ_32929,RMVar_hsa_circ_203995,RMVar_hsa_circ_203993,RMVar_hsa_circ_203991,RMVar_hsa_circ_203988,RMVar_hsa_circ_203989,RMVar_hsa_circ_203987 61323 RMVar_ID_61323 Human_SNP_ID_98803077 m1A Human chr2 + 158625120 158625120 158625120 GCCTCTCCGTACTCACAGAGACCCGCCTCCCCAACAGCTATACGGCGGATTGGGTCAGTCACCTC GCCTCTCCGTACTCACAGAGACCCGCCTCCCCGACAGCTATACGGCGGATTGGGTCAGTCACCTC A G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158621409..158625166 32194978 MeRIP-seq:(Medium) rs1365556783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17279146,Human_RBP_ID_17393047,Human_RBP_ID_17510154 Human_miRNA_ID_843407,Human_miRNA_ID_2366077,Human_miRNA_ID_3013884 RMVar_hsa_circ_61459,RMVar_hsa_circ_93424,RMVar_hsa_circ_323109,RMVar_hsa_circ_290563,RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_203990,RMVar_hsa_circ_32929,RMVar_hsa_circ_203991,RMVar_hsa_circ_328944,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203989,RMVar_hsa_circ_203987,RMVar_hsa_circ_347654,RMVar_hsa_circ_338262,RMVar_hsa_circ_268617,RMVar_hsa_circ_35084,RMVar_hsa_circ_75189,RMVar_hsa_circ_284872,RMVar_hsa_circ_203998,RMVar_hsa_circ_203999,RMVar_hsa_circ_377364,RMVar_hsa_circ_273002,RMVar_hsa_circ_275646,RMVar_hsa_circ_94303,RMVar_hsa_circ_204002,RMVar_hsa_circ_204003,RMVar_hsa_circ_354610,RMVar_hsa_circ_368742,RMVar_hsa_circ_348729,RMVar_hsa_circ_49516 61324 RMVar_ID_61324 Human_SNP_ID_98807150 m1A Human chr2 + 158642508 158642508 158642508 TTCATTCTAGGTGTGTAGGTTAGGGGGAATCAAGCATCTGGTTGACCTTCTGGACCACAGAGTTT TTCATTCTAGGTGTGTAGGTTAGGGGGAATCAGGCATCTGGTTGACCTTCTGGACCACAGAGTTT A G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158634097..158642510 32194978 MeRIP-seq:(Medium) rs750922618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5528056,Human_RBP_ID_8843167,Human_RBP_ID_17504081,Human_RBP_ID_17964222,Human_RBP_ID_22076662,Human_RBP_ID_25575700 Human_Splice_Rec_311788,Human_Splice_Rec_311826,Human_Splice_Rec_311864,Human_Splice_Rec_311900,Human_Splice_Rec_311948,Human_Splice_Rec_311982 Human_miRNA_ID_1423875,Human_miRNA_ID_2727209 RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_32929,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203987,RMVar_hsa_circ_347654,RMVar_hsa_circ_268617,RMVar_hsa_circ_35084,RMVar_hsa_circ_75189,RMVar_hsa_circ_203998,RMVar_hsa_circ_203999,RMVar_hsa_circ_275646,RMVar_hsa_circ_94303,RMVar_hsa_circ_204002,RMVar_hsa_circ_204003,RMVar_hsa_circ_354610,RMVar_hsa_circ_334599,RMVar_hsa_circ_366422 61325 RMVar_ID_61325 Human_SNP_ID_98807151 m1A Human chr2 + 158642508 158642508 158642508 TTCATTCTAGGTGTGTAGGTTAGGGGGAATCAAGCATCTGGTTGACCTTCTGGACCACAGAGTTT TTCATTCTAGGTGTGTAGGTTAGGGGGAATCATGCATCTGGTTGACCTTCTGGACCACAGAGTTT A T PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158634097..158642510 32194978 MeRIP-seq:(Medium) rs750922618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5528056,Human_RBP_ID_8843167,Human_RBP_ID_17504081,Human_RBP_ID_17964222,Human_RBP_ID_22076662,Human_RBP_ID_25575700 Human_Splice_Rec_311788,Human_Splice_Rec_311826,Human_Splice_Rec_311864,Human_Splice_Rec_311900,Human_Splice_Rec_311948,Human_Splice_Rec_311982 Human_miRNA_ID_1423875,Human_miRNA_ID_2727209 RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_32929,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203987,RMVar_hsa_circ_347654,RMVar_hsa_circ_268617,RMVar_hsa_circ_35084,RMVar_hsa_circ_75189,RMVar_hsa_circ_203998,RMVar_hsa_circ_203999,RMVar_hsa_circ_275646,RMVar_hsa_circ_94303,RMVar_hsa_circ_204002,RMVar_hsa_circ_204003,RMVar_hsa_circ_354610,RMVar_hsa_circ_334599,RMVar_hsa_circ_366422 61326 RMVar_ID_61326 Human_SNP_ID_98811849 m1A Human chr2 + 158662952 158662951 158662952 CCTGAGGAACCTGTCCTATCGGCTGGAGCTGGAGGTGCCCCAGGCCCGGTTACTGGGACTGAACG CCTGAGGAACCTGTCCTATCGGCTGGAGCTGG_GGTGCCCCAGGCCCGGTTACTGGGACTGAACG GA G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158662881..158662982 32194978 MeRIP-seq:(Medium) rs770569549 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_829521,Human_RBP_ID_922203,Human_RBP_ID_8843174,Human_RBP_ID_9297539,Human_RBP_ID_19002589,Human_RBP_ID_19098326,Human_RBP_ID_22596457,Human_RBP_ID_22997468,Human_RBP_ID_24560609,Human_RBP_ID_27817681 Human_Splice_Rec_311794,Human_Splice_Rec_311832,Human_Splice_Rec_311870,Human_Splice_Rec_311906,Human_Splice_Rec_311954,Human_Splice_Rec_311988 Human_miRNA_ID_2014949 RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_32929,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203987,RMVar_hsa_circ_268617,RMVar_hsa_circ_75189,RMVar_hsa_circ_203999,RMVar_hsa_circ_94303,RMVar_hsa_circ_204003,RMVar_hsa_circ_31347,RMVar_hsa_circ_55382,RMVar_hsa_circ_16665,RMVar_hsa_circ_265834,RMVar_hsa_circ_362618,RMVar_hsa_circ_50042 61327 RMVar_ID_61327 Human_SNP_ID_98811850 m1A Human chr2 + 158662952 158662952 158662952 CCTGAGGAACCTGTCCTATCGGCTGGAGCTGGAGGTGCCCCAGGCCCGGTTACTGGGACTGAACG CCTGAGGAACCTGTCCTATCGGCTGGAGCTGGGGGTGCCCCAGGCCCGGTTACTGGGACTGAACG A G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158662881..158662982 32194978 MeRIP-seq:(Medium) rs769738027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_829521,Human_RBP_ID_922203,Human_RBP_ID_8843174,Human_RBP_ID_9297539,Human_RBP_ID_19002589,Human_RBP_ID_19098326,Human_RBP_ID_22596457,Human_RBP_ID_22997468,Human_RBP_ID_24560609,Human_RBP_ID_27817681 Human_Splice_Rec_311794,Human_Splice_Rec_311832,Human_Splice_Rec_311870,Human_Splice_Rec_311906,Human_Splice_Rec_311954,Human_Splice_Rec_311988 Human_miRNA_ID_2014949 RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_32929,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203987,RMVar_hsa_circ_268617,RMVar_hsa_circ_75189,RMVar_hsa_circ_203999,RMVar_hsa_circ_94303,RMVar_hsa_circ_204003,RMVar_hsa_circ_31347,RMVar_hsa_circ_55382,RMVar_hsa_circ_16665,RMVar_hsa_circ_265834,RMVar_hsa_circ_362618,RMVar_hsa_circ_50042 61328 RMVar_ID_61328 Human_SNP_ID_98813499 m1A Human chr2 - 158669809 158669809 158669809 CATGTTTTTGCTGGTGACCTCGTGCAGAGCACAGCAGATGGCTGCCATGGTCTCATCAGACAAGA CATGTTTTTGCTGGTGACCTCGTGCAGAGCACCGCAGATGGCTGCCATGGTCTCATCAGACAAGA T G PKP4-AS1 Ensembl:ENSG00000204380 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158669669..158676888 32194978 MeRIP-seq:(Medium) rs757868095 Functional Loss SNV dbSNP153 33..33 33 - - - 61329 RMVar_ID_61329 Human_SNP_ID_98816414 m1A Human chr2 - 158680950 158680950 158680950 TTGACCTACATATCCCCCATTTCATTTCACCCATTTCTCAAACCTCTCATCACGTCACCCACACC TTGACCTACATATCCCCCATTTCATTTCACCCGTTTCTCAAACCTCTCATCACGTCACCCACACC T C PKP4-AS1 Ensembl:ENSG00000204380 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:158680900..158681005 26863196 MeRIP-seq:(Medium) rs1442416428 Functional Loss SNV dbSNP153 33..33 33 - - - 61330 RMVar_ID_61330 Human_SNP_ID_98816503 m1A Human chr2 + 158681332 158681332 158681332 CTTTGGAAGCACAACGTCCAGGCTGGTACCGCAGCGCCATGCCCATTCCTCGCCTCATTCATAGG CTTTGGAAGCACAACGTCCAGGCTGGTACCGCGGCGCCATGCCCATTCCTCGCCTCATTCATAGG A G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158681282..158681383 32194978 MeRIP-seq:(Medium) rs1296785771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22983973 Human_miRNA_ID_2492377,Human_miRNA_ID_2975498 RMVar_hsa_circ_204008,RMVar_hsa_circ_88828,RMVar_hsa_circ_79124,RMVar_hsa_circ_204011 61331 RMVar_ID_61331 Human_SNP_ID_98931255 m1A Human chr2 + 159137269 159137269 159137269 TGGTGCTGTATGGCAGGGAGTGGGTAATAAGTAGGACATGGGAAGACAATATACTGGAGTGGTGG TGGTGCTGTATGGCAGGGAGTGGGTAATAAGTGGGACATGGGAAGACAATATACTGGAGTGGTGG A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159137252..159137403 26863196 MeRIP-seq:(Medium) rs1426216020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4731,RMVar_hsa_circ_67915,RMVar_hsa_circ_296971,RMVar_hsa_circ_298308,RMVar_hsa_circ_35591,RMVar_hsa_circ_97002,RMVar_hsa_circ_285865,RMVar_hsa_circ_321919,RMVar_hsa_circ_361323,RMVar_hsa_circ_378759,RMVar_hsa_circ_327820,RMVar_hsa_circ_120747,RMVar_hsa_circ_273111,RMVar_hsa_circ_99071,RMVar_hsa_circ_204022,RMVar_hsa_circ_204024,RMVar_hsa_circ_51037,RMVar_hsa_circ_204025,RMVar_hsa_circ_204023,RMVar_hsa_circ_204021 61332 RMVar_ID_61332 Human_SNP_ID_98942335 m1A Human chr2 - 159183111 159183111 159183111 AGCAAGGCCCGTCTCTAACCCCAGTCCCCCCAAGTCCCCACTCCTGACTGCTATAGTAGGCCCTA AGCAAGGCCCGTCTCTAACCCCAGTCCCCCCATGTCCCCACTCCTGACTGCTATAGTAGGCCCTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159183109..159183254 26863196 MeRIP-seq:(Medium) rs1011666350 Functional Loss SNV dbSNP153 33..33 33 - - - 61333 RMVar_ID_61333 Human_SNP_ID_98953201 m1A Human chr2 + 159227962 159227962 159227962 TATCTCAATTTGTCGCGATGCCGAAGAAAAACAAATGTAAGCTGTGCCCCTTTATTCCAACCCAG TATCTCAATTTGTCGCGATGCCGAAGAAAAACCAATGTAAGCTGTGCCCCTTTATTCCAACCCAG A C TANC1 Ensembl:ENSG00000115183 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2288110 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19098332 Human_Splice_Rec_312133,Human_Splice_Rec_312151 GWAS_ID_7457,GWAS_ID_7458,GWAS_ID_7459,GWAS_ID_7460,GWAS_ID_7461 RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_89610,RMVar_hsa_circ_204040,RMVar_hsa_circ_204041 61334 RMVar_ID_61334 Human_SNP_ID_98953886 m1A Human chr2 + 159230181 159230181 159230181 GCTGGGAGCAGAACCCAGCATTTAGAGGGAACAGGTACTTTCACTACAAGAGCTGGTTGTGGCCA GCTGGGAGCAGAACCCAGCATTTAGAGGGAACCGGTACTTTCACTACAAGAGCTGGTTGTGGCCA A C TANC1 Ensembl:ENSG00000115183 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3821296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1978493,Human_miRNA_ID_1978494,Human_miRNA_ID_2958627,Human_miRNA_ID_2958628 GWAS_ID_7462,GWAS_ID_7463,GWAS_ID_7464,GWAS_ID_7465,GWAS_ID_7466 RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_89610,RMVar_hsa_circ_204040,RMVar_hsa_circ_204041 61335 RMVar_ID_61335 Human_SNP_ID_98953887 m1A Human chr2 + 159230181 159230181 159230181 GCTGGGAGCAGAACCCAGCATTTAGAGGGAACAGGTACTTTCACTACAAGAGCTGGTTGTGGCCA GCTGGGAGCAGAACCCAGCATTTAGAGGGAACGGGTACTTTCACTACAAGAGCTGGTTGTGGCCA A G TANC1 Ensembl:ENSG00000115183 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3821296 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1978493,Human_miRNA_ID_1978494,Human_miRNA_ID_2958627,Human_miRNA_ID_2958628 GWAS_ID_7462,GWAS_ID_7463,GWAS_ID_7464,GWAS_ID_7465,GWAS_ID_7466 RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_89610,RMVar_hsa_circ_204040,RMVar_hsa_circ_204041 61336 RMVar_ID_61336 Human_SNP_ID_98967543 m1A Human chr2 - 159283038 159283038 159283038 CATGGTGAAACTGATTCACACATTAGCTGATCATGGTGACGATGTCAACTGCTGTGCCTTCTCCT CATGGTGAAACTGATTCACACATTAGCTGATCGTGGTGACGATGTCAACTGCTGTGCCTTCTCCT T C WDSUB1 Ensembl:ENSG00000196151 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159282988..159283108 26863196 MeRIP-seq:(Medium) rs759296460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4584741,Human_RBP_ID_23832800 Human_Splice_Rec_312158,Human_Splice_Rec_312178,Human_Splice_Rec_312190,Human_Splice_Rec_312210,Human_Splice_Rec_312230 Human_miRNA_ID_2721282 RMVar_hsa_circ_306995,RMVar_hsa_circ_350798,RMVar_hsa_circ_204045,RMVar_hsa_circ_14718,RMVar_hsa_circ_302494,RMVar_hsa_circ_275033,RMVar_hsa_circ_204053,RMVar_hsa_circ_204051,RMVar_hsa_circ_204052,RMVar_hsa_circ_288545,RMVar_hsa_circ_316457 61337 RMVar_ID_61337 Human_SNP_ID_98967545 m1A Human chr2 - 159283041 159283041 159283041 GAACATGGTGAAACTGATTCACACATTAGCTGATCATGGTGACGATGTCAACTGCTGTGCCTTCT GAACATGGTGAAACTGATTCACACATTAGCTGTTCATGGTGACGATGTCAACTGCTGTGCCTTCT T A WDSUB1 Ensembl:ENSG00000196151 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:159282990..159283122 26863196 MeRIP-seq:(Medium) rs767210177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_312158,Human_Splice_Rec_312178,Human_Splice_Rec_312190,Human_Splice_Rec_312210,Human_Splice_Rec_312230 Human_miRNA_ID_2721282 RMVar_hsa_circ_306995,RMVar_hsa_circ_350798,RMVar_hsa_circ_204045,RMVar_hsa_circ_14718,RMVar_hsa_circ_302494,RMVar_hsa_circ_275033,RMVar_hsa_circ_204053,RMVar_hsa_circ_204051,RMVar_hsa_circ_204052,RMVar_hsa_circ_288545,RMVar_hsa_circ_316457 61338 RMVar_ID_61338 Human_SNP_ID_98967556 m1A Human chr2 - 159283095 159283095 159283095 GAATAAATAATCTTTATCTGCTTAAAAATTTCAGGCTGTTTTTCTTCAAATAAAGAACATGGTGA GAATAAATAATCTTTATCTGCTTAAAAATTTCCGGCTGTTTTTCTTCAAATAAAGAACATGGTGA T G WDSUB1 Ensembl:ENSG00000196151 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:159283036..159286402 26863410 MeRIP-seq:(Medium) rs569208268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3600901 61339 RMVar_ID_61339 Human_SNP_ID_98968410 m1A Human chr2 + 159286534 159286534 159286534 CCCCGCGCGAGCAGGCCCAGCCGCGCTTCCCCACCTGCCGCCACCGCCGCTGAGCCGGCCCGTGG CCCCGCGCGAGCAGGCCCAGCCGCGCTTCCCCCCCTGCCGCCACCGCCGCTGAGCCGGCCCGTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159286530..159286679 26863196 MeRIP-seq:(Medium) rs1040644799 Functional Loss SNV dbSNP153 33..33 33 - - - 61340 RMVar_ID_61340 Human_SNP_ID_98968453 m1A Human chr2 - 159286644 159286644 159286644 GGCGCCCGCCCCGCCAGCCTCACCTGCGCGGCACGTGACCCGCACCGCCCGTGGGCACCTTGAAG GGCGCCCGCCCCGCCAGCCTCACCTGCGCGGCCCGTGACCCGCACCGCCCGTGGGCACCTTGAAG T G WDSUB1 Ensembl:ENSG00000196151 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:159286519..159286651 26863196 MeRIP-seq:(Medium) rs571357215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_536426,Human_RBP_ID_4584748 Human_Splice_Rec_312157,Human_Splice_Rec_312177,Human_Splice_Rec_312229 61341 RMVar_ID_61341 Human_SNP_ID_98990659 m1A Human chr2 - 159382629 159382629 159382629 TGATGATGACGATGACAGTGATGACCAAGGGGATGAAGATGATGAGGATGAAGAAGATAAAGAAG TGATGATGACGATGACAGTGATGACCAAGGGGGTGAAGATGATGAGGATGAAGAAGATAAAGAAG T C BAZ2B Ensembl:ENSG00000123636 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159382581..159382731 26863196 MeRIP-seq:(Medium) rs1231288026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923076,Human_RBP_ID_6841411,Human_RBP_ID_8257338,Human_RBP_ID_26340011 Human_Splice_Rec_312295,Human_Splice_Rec_312365 RMVar_hsa_circ_59412,RMVar_hsa_circ_72710,RMVar_hsa_circ_352353,RMVar_hsa_circ_69699,RMVar_hsa_circ_69963,RMVar_hsa_circ_63871,RMVar_hsa_circ_36083,RMVar_hsa_circ_78584,RMVar_hsa_circ_44448,RMVar_hsa_circ_204058,RMVar_hsa_circ_204059,RMVar_hsa_circ_21926,RMVar_hsa_circ_313442,RMVar_hsa_circ_37517,RMVar_hsa_circ_204061,RMVar_hsa_circ_204060,RMVar_hsa_circ_296177,RMVar_hsa_circ_289697,RMVar_hsa_circ_365625,RMVar_hsa_circ_42224,RMVar_hsa_circ_53810,RMVar_hsa_circ_67314,RMVar_hsa_circ_310643,RMVar_hsa_circ_73713,RMVar_hsa_circ_67242,RMVar_hsa_circ_53432,RMVar_hsa_circ_204064,RMVar_hsa_circ_360526,RMVar_hsa_circ_204066 61342 RMVar_ID_61342 Human_SNP_ID_98990667 m1A Human chr2 + 159382649 159382646 159382649 TCATCATCTTCATCCCCTTGGTCATCACTGTCATCGTCATCATCATCGTCATAATCACTGTCTCC TCATCATCTTCATCCCCTTGGTCATCACTG___TCGTCATCATCATCGTCATAATCACTGTCTCC GTCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:159382598..159382713 26863196 MeRIP-seq:(Medium) rs1198562195 Functional Loss DEL dbSNP153 31..33 33 - - - 61343 RMVar_ID_61343 Human_SNP_ID_99067719 m1A Human chr2 + 159712652 159712652 159712652 CGAGTGGGACGCGCACTGGTCGGTGCCGGCTCAGGAGCCGGGGTAATGAGCTGCGGAGCTAGTTC CGAGTGGGACGCGCACTGGTCGGTGCCGGCTCGGGAGCCGGGGTAATGAGCTGCGGAGCTAGTTC A G MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:159712556..159712657 32194978 MeRIP-seq:(Medium) rs1336535266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17139094,Human_RBP_ID_22813867,Human_RBP_ID_23833010 Human_Splice_Rec_312621,Human_Splice_Rec_312627 RMVar_hsa_circ_99514,RMVar_hsa_circ_204090 61344 RMVar_ID_61344 Human_SNP_ID_99076642 m1A Human chr2 + 159745936 159745936 159745936 AGTCACCGAAGTGGTGATTTCACAACTTCATCATGTATGTATAAATTACATCAAGTATAACTTCT AGTCACCGAAGTGGTGATTTCACAACTTCATCGTGTATGTATAAATTACATCAAGTATAACTTCT A G MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:159745906..159747874 32194978 MeRIP-seq:(Medium) rs1214582829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2598390,Human_RBP_ID_5528062,Human_RBP_ID_9387569,Human_RBP_ID_18748469,Human_RBP_ID_26338717 Human_Splice_Rec_312587,Human_Splice_Rec_312609,Human_Splice_Rec_312637,Human_Splice_Rec_312649 RMVar_hsa_circ_99514,RMVar_hsa_circ_366916,RMVar_hsa_circ_204090,RMVar_hsa_circ_65907,RMVar_hsa_circ_204097,RMVar_hsa_circ_66716,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_339415,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094,RMVar_hsa_circ_204099,RMVar_hsa_circ_46050,RMVar_hsa_circ_204098,RMVar_hsa_circ_102455,RMVar_hsa_circ_284126,RMVar_hsa_circ_312558,RMVar_hsa_circ_329688,RMVar_hsa_circ_272313,RMVar_hsa_circ_204101,RMVar_hsa_circ_204102,RMVar_hsa_circ_204103,RMVar_hsa_circ_204100,RMVar_hsa_circ_204104,RMVar_hsa_circ_204106,RMVar_hsa_circ_300894,RMVar_hsa_circ_373803,RMVar_hsa_circ_270484,RMVar_hsa_circ_204105 61345 RMVar_ID_61345 Human_SNP_ID_99077495 m1A Human chr2 + 159748854 159748854 159748854 GGAATTCAGCTGATGGTAAAAGTGATAAAACTAAAAGTGCGCCTTCAAGAGATCCAGAAAGATTG GGAATTCAGCTGATGGTAAAAGTGATAAAACTGAAAGTGCGCCTTCAAGAGATCCAGAAAGATTG A G MARCHF7 Ensembl:ENSG00000136536 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:159748671..159752420 32194978 MeRIP-seq:(Medium) rs1223843394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1901157,Human_RBP_ID_8843219,Human_RBP_ID_22077759,Human_RBP_ID_23833081,Human_RBP_ID_27688054 Human_Splice_Rec_312573,Human_Splice_Rec_312589,Human_Splice_Rec_312611,Human_Splice_Rec_312639 Human_miRNA_ID_2854326,Human_miRNA_ID_2857006 RMVar_hsa_circ_99514,RMVar_hsa_circ_366916,RMVar_hsa_circ_204090,RMVar_hsa_circ_65907,RMVar_hsa_circ_204097,RMVar_hsa_circ_66716,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094,RMVar_hsa_circ_204099,RMVar_hsa_circ_46050,RMVar_hsa_circ_204098,RMVar_hsa_circ_102455,RMVar_hsa_circ_312558,RMVar_hsa_circ_329688,RMVar_hsa_circ_272313,RMVar_hsa_circ_204101,RMVar_hsa_circ_204100,RMVar_hsa_circ_204108,RMVar_hsa_circ_204106,RMVar_hsa_circ_300894,RMVar_hsa_circ_270484,RMVar_hsa_circ_204105,RMVar_hsa_circ_204110,RMVar_hsa_circ_297092,RMVar_hsa_circ_319976,RMVar_hsa_circ_356041,RMVar_hsa_circ_310061,RMVar_hsa_circ_118630,RMVar_hsa_circ_204109,RMVar_hsa_circ_204107,RMVar_hsa_circ_204111 61346 RMVar_ID_61346 Human_SNP_ID_99079172 m1A Human chr2 + 159755405 159755404 159755406 GATGTTGAAACAACCAAGGATTTAGTTGGCAAAGAAGGGTAGAGAGCCAGGTGCTGAAGTCATTA GATGTTGAAACAACCAAGGATTTAGTTGGCAA__AAGGGTAGAGAGCCAGGTGCTGAAGTCATTA AAG A MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:159755267..159755581 26863196 MeRIP-seq:(Medium) rs1292352305 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9949697,Human_RBP_ID_22984111 RMVar_hsa_circ_99514,RMVar_hsa_circ_204090,RMVar_hsa_circ_65907,RMVar_hsa_circ_204097,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204096,RMVar_hsa_circ_204099,RMVar_hsa_circ_46050,RMVar_hsa_circ_204098,RMVar_hsa_circ_102455,RMVar_hsa_circ_329688,RMVar_hsa_circ_204110,RMVar_hsa_circ_319976,RMVar_hsa_circ_356041,RMVar_hsa_circ_118630,RMVar_hsa_circ_204109,RMVar_hsa_circ_91413,RMVar_hsa_circ_204111,RMVar_hsa_circ_74484,RMVar_hsa_circ_204112 61347 RMVar_ID_61347 Human_SNP_ID_99086986 m1A Human chr2 - 159783459 159783459 159783459 TGTTCTTCTTTTTTCTACATAGACTGTCCTTCATCTACTTGGATTCAGTTCCAAGACAGTTGTTA TGTTCTTCTTTTTTCTACATAGACTGTCCTTCGTCTACTTGGATTCAGTTCCAAGACAGTTGTTA T C LY75-CD302,CD302 Ensembl:ENSG00000248672,Ensembl:ENSG00000241399 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2114626 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4624797 Human_Splice_Rec_312664,Human_Splice_Rec_312674,Human_Splice_Rec_312690,Human_Splice_Rec_312768,Human_Splice_Rec_312842 GWAS_ID_7467,GWAS_ID_7468,GWAS_ID_7469,GWAS_ID_7470,GWAS_ID_7471,GWAS_ID_7472,GWAS_ID_7473,GWAS_ID_7474,GWAS_ID_7475,GWAS_ID_7476,GWAS_ID_7477,GWAS_ID_7478,GWAS_ID_7479,GWAS_ID_7480,GWAS_ID_7481,GWAS_ID_7482,GWAS_ID_7483,GWAS_ID_7484,GWAS_ID_7485,GWAS_ID_7486,GWAS_ID_7487,GWAS_ID_7488,GWAS_ID_7489,GWAS_ID_7490,GWAS_ID_7491,GWAS_ID_7492,GWAS_ID_7493,GWAS_ID_7494,GWAS_ID_7495,GWAS_ID_7496,GWAS_ID_7497,GWAS_ID_7498,GWAS_ID_7499,GWAS_ID_7500,GWAS_ID_7501,GWAS_ID_7502,GWAS_ID_7503,GWAS_ID_7504,GWAS_ID_7505,GWAS_ID_7506,GWAS_ID_7507,GWAS_ID_7508,GWAS_ID_7509,GWAS_ID_7510,GWAS_ID_7511,GWAS_ID_7512,GWAS_ID_7513,GWAS_ID_7514,GWAS_ID_7515,GWAS_ID_7516,GWAS_ID_7517,GWAS_ID_7518,GWAS_ID_7519,GWAS_ID_7520,GWAS_ID_7521,GWAS_ID_7522,GWAS_ID_7523,GWAS_ID_7524,GWAS_ID_7525,GWAS_ID_7526,GWAS_ID_7527,GWAS_ID_7528,GWAS_ID_7529,GWAS_ID_7530,GWAS_ID_7531,GWAS_ID_7532,GWAS_ID_7533,GWAS_ID_7534,GWAS_ID_7535,GWAS_ID_7536,GWAS_ID_7537,GWAS_ID_7538,GWAS_ID_7539,GWAS_ID_7540,GWAS_ID_7541,GWAS_ID_7542,GWAS_ID_7543,GWAS_ID_7544,GWAS_ID_7545,GWAS_ID_7546,GWAS_ID_7547,GWAS_ID_7548,GWAS_ID_7549,GWAS_ID_7550,GWAS_ID_7551,GWAS_ID_7552,GWAS_ID_7553,GWAS_ID_7554,GWAS_ID_7555,GWAS_ID_7556,GWAS_ID_7557,GWAS_ID_7558,GWAS_ID_7559,GWAS_ID_7560,GWAS_ID_7561,GWAS_ID_7562,GWAS_ID_7563,GWAS_ID_7564,GWAS_ID_7565,GWAS_ID_7566,GWAS_ID_7567,GWAS_ID_7568,GWAS_ID_7569,GWAS_ID_7570,GWAS_ID_7571,GWAS_ID_7572,GWAS_ID_7573,GWAS_ID_7574,GWAS_ID_7575,GWAS_ID_7576,GWAS_ID_7577,GWAS_ID_7578,GWAS_ID_7579,GWAS_ID_7580,GWAS_ID_7581 RMVar_hsa_circ_353371,RMVar_hsa_circ_356989 61348 RMVar_ID_61348 Human_SNP_ID_99152435 m1A Human chr2 - 160062436 160062421 160062437 GCTCTGGGCTCCCGGGATAAGGGGCTCCCGGGACAAGGGGCTCCCGGAGAGCCCAGTGGTTAGCG GCTCTGGGCTCCCGGGATAAGGGGCTCCCGG________________AGAGCCCAGTGGTTAGCG TCCGGGAGCCCCTTGTC T PLA2R1 Ensembl:ENSG00000153246 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:160062386..160062653 26863196 MeRIP-seq:(Medium) rs754716866 Functional Loss DEL dbSNP153 32..47 33 - - - 61349 RMVar_ID_61349 Human_SNP_ID_99152463 m1A Human chr2 + 160062466 160062465 160062466 TGTCCCGGGAGCCCCTTATCCCGGGAGCCCAGAGCCGCGTCCCAAGCACCCGGCCCCGCCGCGCG TGTCCCGGGAGCCCCTTATCCCGGGAGCCCAG_GCCGCGTCCCAAGCACCCGGCCCCGCCGCGCG GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:160062366..160062513 26863196 MeRIP-seq:(Medium) rs1198834502 Functional Loss DEL dbSNP153 33..33 33 - - - 61350 RMVar_ID_61350 Human_SNP_ID_99152465 m1A Human chr2 - 160062473 160062473 160062473 CCGCTTCCGCGCGGCGGGGCCGGGTGCTTGGGACGCGGCTCTGGGCTCCCGGGATAAGGGGCTCC CCGCTTCCGCGCGGCGGGGCCGGGTGCTTGGGTCGCGGCTCTGGGCTCCCGGGATAAGGGGCTCC T A PLA2R1 Ensembl:ENSG00000153246 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:160062466..160062595 26863196 MeRIP-seq:(Medium) rs925409 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7582 61351 RMVar_ID_61351 Human_SNP_ID_99152466 m1A Human chr2 - 160062473 160062473 160062473 CCGCTTCCGCGCGGCGGGGCCGGGTGCTTGGGACGCGGCTCTGGGCTCCCGGGATAAGGGGCTCC CCGCTTCCGCGCGGCGGGGCCGGGTGCTTGGGGCGCGGCTCTGGGCTCCCGGGATAAGGGGCTCC T C PLA2R1 Ensembl:ENSG00000153246 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:160062466..160062595 26863196 MeRIP-seq:(Medium) rs925409 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7582 61352 RMVar_ID_61352 Human_SNP_ID_99225387 m1A Human chr2 - 160364560 160364560 160364560 TTGAGATGACAGGGAAAGGCAGCCCCACCCAGACTCGAAAGAGGGAGTCATGACCCTGGAAAGTG TTGAGATGACAGGGAAAGGCAGCCCCACCCAGGCTCGAAAGAGGGAGTCATGACCCTGGAAAGTG T C RBMS1 Ensembl:ENSG00000153250 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:160364525..160364676 26863196 MeRIP-seq:(Medium) rs896675653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106928,RMVar_hsa_circ_204134,RMVar_hsa_circ_364885,RMVar_hsa_circ_204137 61353 RMVar_ID_61353 Human_SNP_ID_99233670 m1A Human chr2 + 160398888 160398888 160398888 CACCAGCCAAATCTTGTCAATTCTTTCTACACAATATCTTGAATCCATTCTATTTAATACATTCA CACCAGCCAAATCTTGTCAATTCTTTCTACACCATATCTTGAATCCATTCTATTTAATACATTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:160398885..160399119 26863196 MeRIP-seq:(Medium) rs1316916556 Functional Loss SNV dbSNP153 33..33 33 - - - 61354 RMVar_ID_61354 Human_SNP_ID_99235648 m1A Human chr2 + 160407581 160407581 160407581 GGCGGGTGCGGGCGCGGGCGCGGGCGCGGGGCAGCCTCGCCGCGAGGGGGAGGGCGCAAGGAGGT GGCGGGTGCGGGCGCGGGCGCGGGCGCGGGGCTGCCTCGCCGCGAGGGGGAGGGCGCAAGGAGGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:160407455..160408087 26863196 MeRIP-seq:(Medium) rs1399597344 Functional Loss SNV dbSNP153 33..33 33 - - - 61355 RMVar_ID_61355 Human_SNP_ID_99246865 m1A Human chr2 + 160453932 160453932 160453932 TGCTAAGAGTGGCTTTCCAGCCTTCTCCAGCTAACAAAATTCACTCCTCCTTCCCAACCCACTAA TGCTAAGAGTGGCTTTCCAGCCTTCTCCAGCTGACAAAATTCACTCCTCCTTCCCAACCCACTAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:160453930..160454051 26863196 MeRIP-seq:(Medium) rs1441773223 Functional Loss SNV dbSNP153 33..33 33 - - - 61356 RMVar_ID_61356 Human_SNP_ID_99255792 m1A Human chr2 - 160493431 160493431 160493431 GCCGCTGCCGCCGCCGCCGGAAAGGGAGAGGCAGGAGAGCCCGAGACTTGGAAACCCCAAAGTGT GCCGCTGCCGCCGCCGCCGGAAAGGGAGAGGCCGGAGAGCCCGAGACTTGGAAACCCCAAAGTGT T G RBMS1 Ensembl:ENSG00000153250 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:160493229..160493852;chr2:160493216..160493832 26863196 MeRIP-seq:(Medium) rs573204981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5528065,Human_RBP_ID_19000286 61357 RMVar_ID_61357 Human_SNP_ID_99415505 m1A Human chr2 + 161160475 161160475 161160475 GGCGACCTGAGGGGAGAGGGAACGCAGCTGAAAGCGTGAACTGTGTGAGTAAGAAACTTTGTGAA GGCGACCTGAGGGGAGAGGGAACGCAGCTGAAGGCGTGAACTGTGTGAGTAAGAAACTTTGTGAA A G TANK Ensembl:ENSG00000136560 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:161160361..161160596 26863196 MeRIP-seq:(Medium) rs1375013992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1901266,Human_RBP_ID_18421921,Human_RBP_ID_22997209 Human_Splice_Rec_313511,Human_Splice_Rec_313517,Human_Splice_Rec_313521,Human_Splice_Rec_313533,Human_Splice_Rec_313547,Human_Splice_Rec_313561,Human_Splice_Rec_313573,Human_Splice_Rec_313575,Human_Splice_Rec_313583,Human_Splice_Rec_313595,Human_Splice_Rec_313609,Human_Splice_Rec_313615,Human_Splice_Rec_313631 61358 RMVar_ID_61358 Human_SNP_ID_99415514 m1A Human chr2 - 161160509 161160509 161160509 CCGACGTCGTGCTTGACGGATTCGGACACACCAATTCACAAAGTTTCTTACTCACACAGTTCACG CCGACGTCGTGCTTGACGGATTCGGACACACCGATTCACAAAGTTTCTTACTCACACAGTTCACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:161160484..161160571 26863196 MeRIP-seq:(Medium) rs1397209958 Functional Loss SNV dbSNP153 33..33 33 - - - 61359 RMVar_ID_61359 Human_SNP_ID_99415763 m1A Human chr2 + 161161297 161161297 161161297 GTGTTTATCTCACCTCACAGGAGATGCTTTTGACAAGTTATAATAAGGGAGAGATGGTAGTAAAG GTGTTTATCTCACCTCACAGGAGATGCTTTTGGCAAGTTATAATAAGGGAGAGATGGTAGTAAAG A G TANK Ensembl:ENSG00000136560 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:161161284..161161403 26863196 MeRIP-seq:(Medium) rs1258899799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1901267,Human_RBP_ID_22813880 Human_Splice_Rec_313518,Human_Splice_Rec_313534,Human_Splice_Rec_313548,Human_Splice_Rec_313574,Human_Splice_Rec_313610,Human_Splice_Rec_313634 RMVar_hsa_circ_362095 61360 RMVar_ID_61360 Human_SNP_ID_99450691 m1A Human chr2 + 161308493 161308493 161308493 AATGGAATCGGGCTGATTCATCGCCGGTTTGCAGACAGAGCCGCGTCGGGTGTGCGCCGCTGCTG AATGGAATCGGGCTGATTCATCGCCGGTTTGCTGACAGAGCCGCGTCGGGTGTGCGCCGCTGCTG A T PSMD14 Ensembl:ENSG00000115233 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:161308426..161308625;chr2:161308426..161308568 26863196 MeRIP-seq:(Medium) rs1056191022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622731,Human_RBP_ID_9096747,Human_RBP_ID_9330714,Human_RBP_ID_17964226,Human_RBP_ID_22078258,Human_RBP_ID_22452486,Human_RBP_ID_26338718,Human_RBP_ID_26819019,Human_RBP_ID_27002267 Human_miRNA_ID_3068045 RMVar_hsa_circ_77642,RMVar_hsa_circ_204148 61361 RMVar_ID_61361 Human_SNP_ID_99450695 m1A Human chr2 + 161308499 161308499 161308499 ATCGGGCTGATTCATCGCCGGTTTGCAGACAGAGCCGCGTCGGGTGTGCGCCGCTGCTGCTGTTG ATCGGGCTGATTCATCGCCGGTTTGCAGACAGGGCCGCGTCGGGTGTGCGCCGCTGCTGCTGTTG A G PSMD14 Ensembl:ENSG00000115233 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:161308451..161308625 26863196 MeRIP-seq:(Medium) rs1262751841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_829786,Human_RBP_ID_920708,Human_RBP_ID_4622731,Human_RBP_ID_9096747,Human_RBP_ID_9330714,Human_RBP_ID_17964226,Human_RBP_ID_22078258,Human_RBP_ID_22452486,Human_RBP_ID_26338718,Human_RBP_ID_26819019,Human_RBP_ID_27002267 Human_miRNA_ID_3068045 RMVar_hsa_circ_77642,RMVar_hsa_circ_204148 61362 RMVar_ID_61362 Human_SNP_ID_99450710 m1A Human chr2 + 161308551 161308549 161308551 GCTGCTGCTGTTGCCTCTGTCTTCGCGTCACCACAGAGGCAAGACAAGGGTCCATATCGCGGCAT GCTGCTGCTGTTGCCTCTGTCTTCGCGTCAC__CAGAGGCAAGACAAGGGTCCATATCGCGGCAT CCA C PSMD14 Ensembl:ENSG00000115233 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:161308476..161308638 32194978 MeRIP-seq:(Medium) rs1250749742 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_57077,Human_RBP_ID_829786,Human_RBP_ID_4622731,Human_RBP_ID_5470125,Human_RBP_ID_9330714,Human_RBP_ID_17964226,Human_RBP_ID_18442635,Human_RBP_ID_22078258,Human_RBP_ID_26819020 Human_Splice_Rec_313759,Human_Splice_Rec_313781 Human_miRNA_ID_2610752 RMVar_hsa_circ_77642,RMVar_hsa_circ_204148 61363 RMVar_ID_61363 Human_SNP_ID_99464098 m1A Human chr2 - 161367503 161367503 161367503 GGGAAGAGATATAGACTTGTTCTGCTGTGTCCACTGCAGGAGCATCTGTAGGTGGCCCCTAGAAA GGGAAGAGATATAGACTTGTTCTGCTGTGTCCGCTGCAGGAGCATCTGTAGGTGGCCCCTAGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:161367494..161371325 32194978 MeRIP-seq:(Medium) rs1231526511 Functional Loss SNV dbSNP153 33..33 33 - - - 61364 RMVar_ID_61364 Human_SNP_ID_99701988 m1A Human chr2 + 162344206 162344206 162344206 CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGACGCGACTCGAGGGTGACGCTCGCTCCGCTCGT CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGCCGCGACTCGAGGGTGACGCTCGCTCCGCTCGT A C GCA Ensembl:ENSG00000115271 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:162344158..162344271 26863196 MeRIP-seq:(Medium) rs773790858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5422507 Human_Splice_Rec_314889,Human_Splice_Rec_314903,Human_Splice_Rec_314909,Human_Splice_Rec_314919,Human_Splice_Rec_314931 61365 RMVar_ID_61365 Human_SNP_ID_99701989 m1A Human chr2 + 162344206 162344206 162344206 CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGACGCGACTCGAGGGTGACGCTCGCTCCGCTCGT CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGGCGCGACTCGAGGGTGACGCTCGCTCCGCTCGT A G GCA Ensembl:ENSG00000115271 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:162344158..162344271 26863196 MeRIP-seq:(Medium) rs773790858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5422507 Human_Splice_Rec_314889,Human_Splice_Rec_314903,Human_Splice_Rec_314909,Human_Splice_Rec_314919,Human_Splice_Rec_314931 61366 RMVar_ID_61366 Human_SNP_ID_99701990 m1A Human chr2 + 162344206 162344206 162344206 CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGACGCGACTCGAGGGTGACGCTCGCTCCGCTCGT CTGCGCCTGTGCTTTTTCTCCCAGCACTGCGGTCGCGACTCGAGGGTGACGCTCGCTCCGCTCGT A T GCA Ensembl:ENSG00000115271 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:162344158..162344271 26863196 MeRIP-seq:(Medium) rs773790858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5422507 Human_Splice_Rec_314889,Human_Splice_Rec_314903,Human_Splice_Rec_314909,Human_Splice_Rec_314919,Human_Splice_Rec_314931 61367 RMVar_ID_61367 Human_SNP_ID_99702009 m1A Human chr2 - 162344226 162344226 162344226 GGTAGGCCATGACGAGCGGGACGAGCGGAGCGAGCGTCACCCTCGAGTCGCGTCCGCAGTGCTGG GGTAGGCCATGACGAGCGGGACGAGCGGAGCGTGCGTCACCCTCGAGTCGCGTCCGCAGTGCTGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:162344176..162344275 26863196 MeRIP-seq:(Medium) rs764942681 Functional Loss SNV dbSNP153 33..33 33 - - - 61368 RMVar_ID_61368 Human_SNP_ID_100037550 m1A Human chr2 - 163736171 163736171 163736171 TGCCCGTCTCTCTCCACTGCCCGCCTCTCGCCACTGCCTCCCGTCTTCTCTCCCTCACGGCAGCC TGCCCGTCTCTCTCCACTGCCCGCCTCTCGCCGCTGCCTCCCGTCTTCTCTCCCTCACGGCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:163736123..163736309 26863196 MeRIP-seq:(Medium) rs974275245 Functional Loss SNV dbSNP153 33..33 33 - - - 61369 RMVar_ID_61369 Human_SNP_ID_100037554 m1A Human chr2 + 163736178 163736178 163736178 GTGAGGGAGAGAAGACGGGAGGCAGTGGCGAGAGGCGGGCAGTGGAGAGAGACGGGCAGCGGGAG GTGAGGGAGAGAAGACGGGAGGCAGTGGCGAGGGGCGGGCAGTGGAGAGAGACGGGCAGCGGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:163736132..163736389;chr2:163736069..163736340 26863196 MeRIP-seq:(Medium) rs1027302073 Functional Loss SNV dbSNP153 33..33 33 - - - 61370 RMVar_ID_61370 Human_SNP_ID_100037751 m1A Human chr2 - 163736644 163736644 163736644 GGCCGCAGCTGTCGAGAGGGCCGGGAACCGGCAGGGAAGAGCCCGCGGGCCGGGGAGCAGCGCGG GGCCGCAGCTGTCGAGAGGGCCGGGAACCGGCCGGGAAGAGCCCGCGGGCCGGGGAGCAGCGCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:163736573..163736830 26863196 MeRIP-seq:(Medium) rs553809903 Functional Loss SNV dbSNP153 33..33 33 - - - 61371 RMVar_ID_61371 Human_SNP_ID_100301071 m1A Human chr2 + 164841302 164841302 164841302 TCAGGGCGGGACGCGCGCCTTCCCGAGGCCGGAGCGAAGCTGGCTGAGCGTCAAGAGCCCGCCCG TCAGGGCGGGACGCGCGCCTTCCCGAGGCCGGGGCGAAGCTGGCTGAGCGTCAAGAGCCCGCCCG A G AC019197.1 Ensembl:ENSG00000236283 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:164841210..164841336 26863196 MeRIP-seq:(Medium) rs980008698 Functional Loss SNV dbSNP153 33..33 33 - - - 61372 RMVar_ID_61372 Human_SNP_ID_290442383 m1A Human chr6 + 105179862 105179862 105179862 TACCTTTCCTTCCCAGCCCTGCCCGGAGCTTCAGCCCGGCGCCCGCAGAAGTTTCCCGGCGGAGC TACCTTTCCTTCCCAGCCCTGCCCGGAGCTTCCGCCCGGCGCCCGCAGAAGTTTCCCGGCGGAGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:105179850..105179934 26863196 MeRIP-seq:(Medium) rs894011150 Functional Loss SNV dbSNP153 33..33 33 - - - 61373 RMVar_ID_61373 Human_SNP_ID_290442388 m1A Human chr6 - 105179882 105179882 105179882 GGGCCACCCGGGTCAAGCGCGCTCCGCCGGGAAACTTCTGCGGGCGCCGGGCTGAAGCTCCGGGC GGGCCACCCGGGTCAAGCGCGCTCCGCCGGGAGACTTCTGCGGGCGCCGGGCTGAAGCTCCGGGC T C POPDC3 Ensembl:ENSG00000132429 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:105179788..105179973 26863196 MeRIP-seq:(Medium) rs1433659628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5427698 Human_Splice_Rec_798733,Human_Splice_Rec_798745 61374 RMVar_ID_61374 Human_SNP_ID_290442435 m1A Human chr6 - 105179996 105179996 105179996 CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGAGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGGGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC T C POPDC3 Ensembl:ENSG00000132429 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:105179895..105179995 26863410 MeRIP-seq:(Medium) rs1365044018 Functional Loss SNV dbSNP153 33..33 33 - - - 61375 RMVar_ID_61375 Human_SNP_ID_290442436 m1A Human chr6 - 105179996 105179996 105179996 CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGAGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGCGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC T G POPDC3 Ensembl:ENSG00000132429 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:105179895..105179995 26863410 MeRIP-seq:(Medium) rs1365044018 Functional Loss SNV dbSNP153 33..33 33 - - - 61376 RMVar_ID_61376 Human_SNP_ID_290494750 m1A Human chr6 + 105402913 105402913 105402913 AGGGACAGCATGGCCGGGGACAGGCAGGGGGCAGCGTGGAGGGGCGCGGGCTCCGGGAGCGGACC AGGGACAGCATGGCCGGGGACAGGCAGGGGGCGGCGTGGAGGGGCGCGGGCTCCGGGAGCGGACC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:105402876..105403016 26863196 MeRIP-seq:(Medium) rs753279673 Functional Loss SNV dbSNP153 33..33 33 - - - 61377 RMVar_ID_61377 Human_SNP_ID_290494751 m1A Human chr6 + 105402913 105402913 105402913 AGGGACAGCATGGCCGGGGACAGGCAGGGGGCAGCGTGGAGGGGCGCGGGCTCCGGGAGCGGACC AGGGACAGCATGGCCGGGGACAGGCAGGGGGCTGCGTGGAGGGGCGCGGGCTCCGGGAGCGGACC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:105402876..105403016 26863196 MeRIP-seq:(Medium) rs753279673 Functional Loss SNV dbSNP153 33..33 33 - - - 61378 RMVar_ID_61378 Human_SNP_ID_290494796 m1A Human chr6 + 105403010 105403010 105403010 GGGGCGCAGGCAGCTGCGGGGCGGCCGGCGGCAGCGGGCGGCCGGCTCACGGCCAGAGCTAGCAC GGGGCGCAGGCAGCTGCGGGGCGGCCGGCGGCCGCGGGCGGCCGGCTCACGGCCAGAGCTAGCAC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr6:105402911..105403035 26863410 MeRIP-seq:(Medium) rs1444693585 Functional Loss SNV dbSNP153 33..33 33 - - - 61379 RMVar_ID_61379 Human_SNP_ID_290494797 m1A Human chr6 + 105403010 105403010 105403010 GGGGCGCAGGCAGCTGCGGGGCGGCCGGCGGCAGCGGGCGGCCGGCTCACGGCCAGAGCTAGCAC GGGGCGCAGGCAGCTGCGGGGCGGCCGGCGGCGGCGGGCGGCCGGCTCACGGCCAGAGCTAGCAC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr6:105402911..105403035 26863410 MeRIP-seq:(Medium) rs1444693585 Functional Loss SNV dbSNP153 33..33 33 - - - 61380 RMVar_ID_61380 Human_SNP_ID_290697752 m1A Human chr6 - 106269596 106269596 106269596 GGGTGTACTGGGTCCCCCAGCAGTGACGGCCCACCGGCGCTGCACTCGATTTCTCACCTGGCCTT GGGTGTACTGGGTCCCCCAGCAGTGACGGCCCTCCGGCGCTGCACTCGATTTCTCACCTGGCCTT T A ATG5 Ensembl:ENSG00000057663 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:106269470..106269638 26863196 MeRIP-seq:(Medium) rs954967088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284976,RMVar_hsa_circ_240686,RMVar_hsa_circ_240688,RMVar_hsa_circ_271706,RMVar_hsa_circ_295174,RMVar_hsa_circ_352323,RMVar_hsa_circ_72608,RMVar_hsa_circ_240687 61381 RMVar_ID_61381 Human_SNP_ID_290710745 m1A Human chr6 - 106323909 106323908 106323910 TACTAGCTAGTTTGACTGGAAAATAATGAACAAGAGGGAAAGAAGTAGTGGATACTTAGGTGGAA TACTAGCTAGTTTGACTGGAAAATAATGAAC__GAGGGAAAGAAGTAGTGGATACTTAGGTGGAA CTT C ATG5 Ensembl:ENSG00000057663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:106323907..106323992 26863196 MeRIP-seq:(Medium) rs1420392558 Functional Loss DEL dbSNP153 32..33 33 - - - 61382 RMVar_ID_61382 Human_SNP_ID_290781056 m1A Human chr6 - 106612623 106612617 106612623 AATTGTAAAAGGTTGCTTTATGAGGAAGTTTAAAAGTAGAAGGCAAAGAATTGAACATACTGACA AATTGTAAAAGGTTGCTTTATGAGGAAGTTTA______GAAGGCAAAGAATTGAACATACTGACA CTACTTT C RTN4IP1 Ensembl:ENSG00000130347 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:106612621..106612762 26863196 MeRIP-seq:(Medium) rs1375900589 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_308896,RMVar_hsa_circ_374041,RMVar_hsa_circ_240694,RMVar_hsa_circ_240696,RMVar_hsa_circ_329411 61383 RMVar_ID_61383 Human_SNP_ID_290785234 m1A Human chr6 + 106629673 106629673 106629673 CCTTGCCTGGCTCCTGTGGTGGCAGGCTGGGCACGAGGACCATGCTGGGCCGGAGCCTCCGAGAA CCTTGCCTGGCTCCTGTGGTGGCAGGCTGGGCTCGAGGACCATGCTGGGCCGGAGCCTCCGAGAA A T QRSL1 Ensembl:ENSG00000130348 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:106629623..106629710 26863196 MeRIP-seq:(Medium) rs1224073433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4858944 Human_Splice_Rec_799193,Human_Splice_Rec_799213,Human_Splice_Rec_799219 61384 RMVar_ID_61384 Human_SNP_ID_290785243 m1A Human chr6 + 106629694 106629694 106629694 GCAGGCTGGGCACGAGGACCATGCTGGGCCGGAGCCTCCGAGAAGTGAGTGGAATTGGCCCGCTG GCAGGCTGGGCACGAGGACCATGCTGGGCCGGGGCCTCCGAGAAGTGAGTGGAATTGGCCCGCTG A G QRSL1 Ensembl:ENSG00000130348 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:106629646..106629749 26863196 MeRIP-seq:(Medium) rs1388731180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904200 Human_Splice_Rec_799193,Human_Splice_Rec_799213,Human_Splice_Rec_799219 61385 RMVar_ID_61385 Human_SNP_ID_290879990 m1A Human chr6 + 107028268 107028268 107028268 CGGCCGCGGGGAGGGACGAGAGGGCCTGACGTACAGGTGAGTGCGCCTCTGCTGGCGCGCCGCGC CGGCCGCGGGGAGGGACGAGAGGGCCTGACGTCCAGGTGAGTGCGCCTCTGCTGGCGCGCCGCGC A C MTRES1 Ensembl:ENSG00000130349 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:107028218..107028449 26863196 MeRIP-seq:(Medium) rs1486686097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4859028,Human_RBP_ID_19129628 Human_Splice_Rec_799601 61386 RMVar_ID_61386 Human_SNP_ID_290879991 m1A Human chr6 + 107028268 107028268 107028268 CGGCCGCGGGGAGGGACGAGAGGGCCTGACGTACAGGTGAGTGCGCCTCTGCTGGCGCGCCGCGC CGGCCGCGGGGAGGGACGAGAGGGCCTGACGTGCAGGTGAGTGCGCCTCTGCTGGCGCGCCGCGC A G MTRES1 Ensembl:ENSG00000130349 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:107028218..107028449 26863196 MeRIP-seq:(Medium) rs1486686097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4859028,Human_RBP_ID_19129628 Human_Splice_Rec_799601 61387 RMVar_ID_61387 Human_SNP_ID_290904017 m1A Human chr6 - 107115105 107115105 107115105 CAAACTCGGCGCGGGCCCGCCCGGCAAAGTACAGAACTCGCGTCCCAGGTAAGTGCGGGGCGGAT CAAACTCGGCGCGGGCCCGCCCGGCAAAGTACGGAACTCGCGTCCCAGGTAAGTGCGGGGCGGAT T C BEND3 Ensembl:ENSG00000178409 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:107115103..107115255 26863196 MeRIP-seq:(Medium) rs1554239104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_799623 61388 RMVar_ID_61388 Human_SNP_ID_290991326 m1A Human chr6 + 107490199 107490199 107490199 CGCGCCGGCCCTTGCTCCCCGCGCCCATGCGGACGGACCGAGCGACGGAAGATGGCTGACGACTC CGCGCCGGCCCTTGCTCCCCGCGCCCATGCGGGCGGACCGAGCGACGGAAGATGGCTGACGACTC A G SOBP Ensembl:ENSG00000112320 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:107490112..107490199 26863410 MeRIP-seq:(Medium) rs1244092552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252055,Human_RBP_ID_4905057,Human_RBP_ID_9400984,Human_RBP_ID_15587601,Human_RBP_ID_24126842 61389 RMVar_ID_61389 Human_SNP_ID_290991380 m1A Human chr6 + 107490304 107490304 107490304 GGAGCGGCAGCGGCAGCGAGGGCGGCAGGGGCAGCGGCAGCAGCGGCGGCGTTGGCTGCGGCGGC GGAGCGGCAGCGGCAGCGAGGGCGGCAGGGGCTGCGGCAGCAGCGGCGGCGTTGGCTGCGGCGGC A T SOBP Ensembl:ENSG00000112320 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:107490065..107490369 26863196 MeRIP-seq:(Medium) rs1390225351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9402493 61390 RMVar_ID_61390 Human_SNP_ID_291023805 m1A Human chr6 + 107634094 107634094 107634094 GATCCGCCCGCCCTTCATCCGCGGGCCTCCGCACCATGCCTCCAACCCCAACAGCCCCCTGTCCA GATCCGCCCGCCCTTCATCCGCGGGCCTCCGCTCCATGCCTCCAACCCCAACAGCCCCCTGTCCA A T SOBP Ensembl:ENSG00000112320 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:107633995..107634095 26863410 MeRIP-seq:(Medium) rs1003519427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17537944 61391 RMVar_ID_61391 Human_SNP_ID_291081472 m1A Human chr6 - 107871714 107871714 107871714 TAGCTTTGAGGAAGAAGAGGAGGAAGAAGAAGATGATGACTAAGCAGTACTCTGAATGGACCACA TAGCTTTGAGGAAGAAGAGGAGGAAGAAGAAGGTGATGACTAAGCAGTACTCTGAATGGACCACA T C SEC63 Ensembl:ENSG00000025796 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:107871616..107871845 26863196 MeRIP-seq:(Medium) rs1479640940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_650087,Human_RBP_ID_840881,Human_RBP_ID_2003950,Human_RBP_ID_2962694,Human_RBP_ID_4906102,Human_RBP_ID_7513536,Human_RBP_ID_9185178,Human_RBP_ID_9400986,Human_RBP_ID_19029265,Human_RBP_ID_23067427,Human_RBP_ID_23120293,Human_RBP_ID_24548471,Human_RBP_ID_25949355,Human_RBP_ID_26354303,Human_RBP_ID_27827941 Human_miRNA_ID_158091 61392 RMVar_ID_61392 Human_SNP_ID_291081473 m1A Human chr6 - 107871714 107871714 107871714 TAGCTTTGAGGAAGAAGAGGAGGAAGAAGAAGATGATGACTAAGCAGTACTCTGAATGGACCACA TAGCTTTGAGGAAGAAGAGGAGGAAGAAGAAGCTGATGACTAAGCAGTACTCTGAATGGACCACA T G SEC63 Ensembl:ENSG00000025796 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:107871616..107871845 26863196 MeRIP-seq:(Medium) rs1479640940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_650087,Human_RBP_ID_840881,Human_RBP_ID_2003950,Human_RBP_ID_2962694,Human_RBP_ID_4906102,Human_RBP_ID_7513536,Human_RBP_ID_9185178,Human_RBP_ID_9400986,Human_RBP_ID_19029265,Human_RBP_ID_23067427,Human_RBP_ID_23120293,Human_RBP_ID_24548471,Human_RBP_ID_25949355,Human_RBP_ID_26354303,Human_RBP_ID_27827941 Human_miRNA_ID_158091 61393 RMVar_ID_61393 Human_SNP_ID_291087170 m1A Human chr6 - 107893478 107893478 107893478 AAAAGCAGGCAAATGGAGTCGTTGGGAATGTAAGTTTATTATTATCGTTATTATCATTATTAAGC AAAAGCAGGCAAATGGAGTCGTTGGGAATGTAGGTTTATTATTATCGTTATTATCATTATTAAGC T C SEC63 Ensembl:ENSG00000025796 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:107893476..107893525 26863196 MeRIP-seq:(Medium) rs375648715 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_12467,RMVar_hsa_circ_48741,RMVar_hsa_circ_59053,RMVar_hsa_circ_266285,RMVar_hsa_circ_320968,RMVar_hsa_circ_268737,RMVar_hsa_circ_35889,RMVar_hsa_circ_40943,RMVar_hsa_circ_16249,RMVar_hsa_circ_50211,RMVar_hsa_circ_286430,RMVar_hsa_circ_311110,RMVar_hsa_circ_363891,RMVar_hsa_circ_364853,RMVar_hsa_circ_325358,RMVar_hsa_circ_58939,RMVar_hsa_circ_240721,RMVar_hsa_circ_240722 61394 RMVar_ID_61394 Human_SNP_ID_291087224 m1A Human chr6 - 107893626 107893626 107893626 CAGCAGGGTGAAACTAACAAGAACAGGACAAAAGGAGGATGGCAACAGAAGAGTAAAGGACCCAA CAGCAGGGTGAAACTAACAAGAACAGGACAAAGGGAGGATGGCAACAGAAGAGTAAAGGACCCAA T C SEC63 Ensembl:ENSG00000025796 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:107893435..107893676 26863196 MeRIP-seq:(Medium) rs768317798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840455,Human_RBP_ID_952040,Human_RBP_ID_2003972,Human_RBP_ID_2962777,Human_RBP_ID_7513628,Human_RBP_ID_18538793,Human_RBP_ID_22618976,Human_RBP_ID_27518608,Human_RBP_ID_27827947 Human_Splice_Rec_799810 RMVar_hsa_circ_12467,RMVar_hsa_circ_48741,RMVar_hsa_circ_59053,RMVar_hsa_circ_266285,RMVar_hsa_circ_320968,RMVar_hsa_circ_268737,RMVar_hsa_circ_35889,RMVar_hsa_circ_40943,RMVar_hsa_circ_16249,RMVar_hsa_circ_67481,RMVar_hsa_circ_50211,RMVar_hsa_circ_286430,RMVar_hsa_circ_311110,RMVar_hsa_circ_363891,RMVar_hsa_circ_364853,RMVar_hsa_circ_325358,RMVar_hsa_circ_58939,RMVar_hsa_circ_336658,RMVar_hsa_circ_240721,RMVar_hsa_circ_240722,RMVar_hsa_circ_364559,RMVar_hsa_circ_73611,RMVar_hsa_circ_313956,RMVar_hsa_circ_71243,RMVar_hsa_circ_17886,RMVar_hsa_circ_57040,RMVar_hsa_circ_240723,RMVar_hsa_circ_240724 61395 RMVar_ID_61395 Human_SNP_ID_291087225 m1A Human chr6 - 107893631 107893631 107893631 ATTCACAGCAGGGTGAAACTAACAAGAACAGGACAAAAGGAGGATGGCAACAGAAGAGTAAAGGA ATTCACAGCAGGGTGAAACTAACAAGAACAGGGCAAAAGGAGGATGGCAACAGAAGAGTAAAGGA T C SEC63 Ensembl:ENSG00000025796 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:107893444..107893655 26863196 MeRIP-seq:(Medium) rs776315483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840455,Human_RBP_ID_952040,Human_RBP_ID_2003972,Human_RBP_ID_2962777,Human_RBP_ID_18538793,Human_RBP_ID_22618976,Human_RBP_ID_25949422,Human_RBP_ID_27518608,Human_RBP_ID_27827947 Human_Splice_Rec_799810 RMVar_hsa_circ_12467,RMVar_hsa_circ_48741,RMVar_hsa_circ_59053,RMVar_hsa_circ_266285,RMVar_hsa_circ_320968,RMVar_hsa_circ_268737,RMVar_hsa_circ_35889,RMVar_hsa_circ_40943,RMVar_hsa_circ_16249,RMVar_hsa_circ_67481,RMVar_hsa_circ_50211,RMVar_hsa_circ_286430,RMVar_hsa_circ_311110,RMVar_hsa_circ_363891,RMVar_hsa_circ_364853,RMVar_hsa_circ_325358,RMVar_hsa_circ_58939,RMVar_hsa_circ_336658,RMVar_hsa_circ_240721,RMVar_hsa_circ_240722,RMVar_hsa_circ_364559,RMVar_hsa_circ_73611,RMVar_hsa_circ_313956,RMVar_hsa_circ_71243,RMVar_hsa_circ_17886,RMVar_hsa_circ_57040,RMVar_hsa_circ_240723,RMVar_hsa_circ_240724 61396 RMVar_ID_61396 Human_SNP_ID_291104585 m1A Human chr6 - 107957999 107957999 107957999 GCGAGGCGGAGGAGGGGGTGCCATGGCCGGGCAGCAGTTCCAGTACGATGACAGTGGGAACACCT GCGAGGCGGAGGAGGGGGTGCCATGGCCGGGCGGCAGTTCCAGTACGATGACAGTGGGAACACCT T C SEC63 Ensembl:ENSG00000025796 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:107957707..107958175 26863196 MeRIP-seq:(Medium) rs1389875293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251926,Human_RBP_ID_650101,Human_RBP_ID_840778,Human_RBP_ID_2962932,Human_RBP_ID_4903455,Human_RBP_ID_7514013,Human_RBP_ID_15590386,Human_RBP_ID_18059765,Human_RBP_ID_18449329,Human_RBP_ID_18850995,Human_RBP_ID_22105333,Human_RBP_ID_24127151 61397 RMVar_ID_61397 Human_SNP_ID_291104592 m1A Human chr6 + 107958013 107958013 107958013 TCATCGTACTGGAACTGCTGCCCGGCCATGGCACCCCCTCCTCCGCCTCGCTCTTCTCACCGCCG TCATCGTACTGGAACTGCTGCCCGGCCATGGCTCCCCCTCCTCCGCCTCGCTCTTCTCACCGCCG A T AL024507.3 Ensembl:ENSG00000272476 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:107957974..107958176 26863196 MeRIP-seq:(Medium) rs752767941 Functional Loss SNV dbSNP153 33..33 33 - - - 61398 RMVar_ID_61398 Human_SNP_ID_291104631 m1A Human chr6 + 107958092 107958092 107958092 CTCTGCACTCCCGCTCCCAACGCCCCGGCCCGAGTGGCGTAGCTTGGACACTGCCGCCGCCGCCT CTCTGCACTCCCGCTCCCAACGCCCCGGCCCGGGTGGCGTAGCTTGGACACTGCCGCCGCCGCCT A G AL024507.3 Ensembl:ENSG00000272476 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:107957976..107958205;chr6:107957876..107958254 26863196 MeRIP-seq:(Medium) rs1373686353 Functional Loss SNV dbSNP153 33..33 33 - - - 61399 RMVar_ID_61399 Human_SNP_ID_291104642 m1A Human chr6 - 107958124 107958121 107958124 GTCCGTGAGAGTGGCGTGGGGGCGGGGAGGAGAGGCGGCGGCGGCAGTGTCCAAGCTACGCCACT GTCCGTGAGAGTGGCGTGGGGGCGGGGAGGAG___CGGCGGCGGCAGTGTCCAAGCTACGCCACT GCCT G SEC63 Ensembl:ENSG00000025796 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:107958032..107958205 26863410 MeRIP-seq:(Medium) rs1474706958 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_791856,Human_RBP_ID_840779,Human_RBP_ID_4903456,Human_RBP_ID_5399888 61400 RMVar_ID_61400 Human_SNP_ID_291116105 m1A Human chr6 - 108005104 108005104 108005104 CAGCTGGAGAAGGACTTCAGCAGCATGAAGAAATACTGCCACGTCATCCGCGTCATTGCCCACAC CAGCTGGAGAAGGACTTCAGCAGCATGAAGAAGTACTGCCACGTCATCCGCGTCATTGCCCACAC T C RPL3P7 Ensembl:ENSG00000225093 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879108277 Functional Loss SNV dbSNP153 33..33 33 - - - 61401 RMVar_ID_61401 Human_SNP_ID_291131447 m1A Human chr6 - 108068582 108068582 108068582 GGAGAAATGGGTGGATTTCAGAGATACTTAGGAGGCAGAAATTACAGGCTTGGAGGTTAATTGAA GGAGAAATGGGTGGATTTCAGAGATACTTAGGTGGCAGAAATTACAGGCTTGGAGGTTAATTGAA T A OSTM1 Ensembl:ENSG00000081087 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:108068580..108068682 26863196 MeRIP-seq:(Medium) rs898890111 Functional Loss SNV dbSNP153 33..33 33 - - - 61402 RMVar_ID_61402 Human_SNP_ID_291133025 m1A Human chr6 + 108074616 108074616 108074616 AGCAGCCCCAGCGGCAGCCACGGCGGCAACGAACACCTCCGCTGCGCGGCTGTCGGGCCCGGCTC AGCAGCCCCAGCGGCAGCCACGGCGGCAACGACCACCTCCGCTGCGCGGCTGTCGGGCCCGGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:108074569..108074715 26863196 MeRIP-seq:(Medium) rs119460973 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_223 61403 RMVar_ID_61403 Human_SNP_ID_291133026 m1A Human chr6 + 108074616 108074616 108074616 AGCAGCCCCAGCGGCAGCCACGGCGGCAACGAACACCTCCGCTGCGCGGCTGTCGGGCCCGGCTC AGCAGCCCCAGCGGCAGCCACGGCGGCAACGATCACCTCCGCTGCGCGGCTGTCGGGCCCGGCTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:108074569..108074715 26863196 MeRIP-seq:(Medium) rs119460973 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_223 61404 RMVar_ID_61404 Human_SNP_ID_291133033 m1A Human chr6 - 108074636 108074636 108074636 GGTGTGTGAGCCCGGTGATGGAGCCGGGCCCGACAGCCGCGCAGCGGAGGTGTTCGTTGCCGCCG GGTGTGTGAGCCCGGTGATGGAGCCGGGCCCGTCAGCCGCGCAGCGGAGGTGTTCGTTGCCGCCG T A OSTM1 Ensembl:ENSG00000081087 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:108074587..108074696 26863196 MeRIP-seq:(Medium) rs1562378515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903460 61405 RMVar_ID_61405 Human_SNP_ID_291133065 m1A Human chr6 + 108074680 108074680 108074680 CCATCACCGGGCTCACACACCCCAGGGAGCCCACCGCCGCCTCTCCGCCCCCAGCCGGCACCGCG CCATCACCGGGCTCACACACCCCAGGGAGCCCCCCGCCGCCTCTCCGCCCCCAGCCGGCACCGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:108074590..108074692 26863196 MeRIP-seq:(Medium) rs945582334 Functional Loss SNV dbSNP153 33..33 33 - - - 61406 RMVar_ID_61406 Human_SNP_ID_291168791 m1A Human chr6 - 108222962 108222958 108222962 AGTGACTTTGAATGGCTGCGAAGTGAATTAGAAAGAGAGAGCAAGGTAAGAATGATTTATGATGC AGTGACTTTGAATGGCTGCGAAGTGAATTAGA____GAGAGCAAGGTAAGAATGATTTATGATGC CTCTT C SNX3 Ensembl:ENSG00000112335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:108222951..108223109 26863196 MeRIP-seq:(Medium) rs769873992 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_4906144,Human_RBP_ID_15590734,Human_RBP_ID_24127270 Human_Splice_Rec_799970,Human_Splice_Rec_799971,Human_Splice_Rec_799980,Human_Splice_Rec_799981,Human_Splice_Rec_799988,Human_Splice_Rec_799989 Human_miRNA_ID_2911647 RMVar_hsa_circ_86247,RMVar_hsa_circ_240755,RMVar_hsa_circ_309640,RMVar_hsa_circ_301194 61407 RMVar_ID_61407 Human_SNP_ID_291178689 m1A Human chr6 - 108260936 108260936 108260936 CGGAGGGGGCGGAGGGAGCCCGCGGCGGCGGCAGCAGCTACAGCGAAATGGCGGAGACCGTGGCT CGGAGGGGGCGGAGGGAGCCCGCGGCGGCGGCGGCAGCTACAGCGAAATGGCGGAGACCGTGGCT T C SNX3 Ensembl:ENSG00000112335 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:108260726..108261198;chr6:108260751..108261216 26863196 MeRIP-seq:(Medium) rs751463571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841609,Human_RBP_ID_4903462,Human_RBP_ID_7514413,Human_RBP_ID_9336256 RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 61408 RMVar_ID_61408 Human_SNP_ID_291178727 m1A Human chr6 + 108260974 108260969 108260975 CGCCGCGGGCTCCCTCCGCCCCCTCCGCGTTCAGCCGCCGCCGCCGCCGCTGCTGCCCGCCGTGG CGCCGCGGGCTCCCTCCGCCCCCTCCGC______CCGCCGCCGCCGCCGCTGCTGCCCGCCGTGG CGTTCAG C lnc-AFG1L-4,lnc-AFG1L-4:2,RF00017-4494,lnc-AFG1L-4:3 RNACentral:URS00008B3953,RNACentral:URS00008B4FC8,RNACentral:URS00009086DB,RNACentral:URS00008B9853 lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:108260926..108260975 32194978 MeRIP-seq:(Medium) rs142951692 Functional Loss DEL dbSNP153 29..34 33 - - - 61409 RMVar_ID_61409 Human_SNP_ID_291178733 m1A Human chr6 + 108260974 108260973 108260975 CGCCGCGGGCTCCCTCCGCCCCCTCCGCGTTCAGCCGCCGCCGCCGCCGCTGCTGCCCGCCGTGG CGCCGCGGGCTCCCTCCGCCCCCTCCGCGTTC__CCGCCGCCGCCGCCGCTGCTGCCCGCCGTGG CAG C lnc-AFG1L-4,lnc-AFG1L-4:2,RF00017-4494,lnc-AFG1L-4:3 RNACentral:URS00008B3953,RNACentral:URS00008B4FC8,RNACentral:URS00009086DB,RNACentral:URS00008B9853 lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:108260926..108260975 32194978 MeRIP-seq:(Medium) rs1491401907 Functional Loss DEL dbSNP153 33..34 33 - - - 61410 RMVar_ID_61410 Human_SNP_ID_291244633 m1A Human chr6 - 108558269 108558269 108558269 GTGGGAGGGTTCAAGGGGGGACGCGAGAGGACAGCGGACGGGAGGAAGGCAGCCGACTTGGGGCG GTGGGAGGGTTCAAGGGGGGACGCGAGAGGACGGCGGACGGGAGGAAGGCAGCCGACTTGGGGCG T C AL139106.1 Ensembl:ENSG00000287044 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:108558218..108558298 26863196 MeRIP-seq:(Medium) rs889204545 Functional Loss SNV dbSNP153 33..33 33 - - - 61411 RMVar_ID_61411 Human_SNP_ID_291246306 m1A Human chr6 + 108562139 108562139 108562139 AGTACATTTGCTGGATTCTCCGGACAGCACCGAGGAGGTAGGTCCGCAGCCAACTTTGGAGTAGA AGTACATTTGCTGGATTCTCCGGACAGCACCGTGGAGGTAGGTCCGCAGCCAACTTTGGAGTAGA A T FOXO3 Ensembl:ENSG00000118689 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:108562028..108562189 26863196 MeRIP-seq:(Medium) rs1308327847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15591579,Human_RBP_ID_22106889,Human_RBP_ID_26771949 61412 RMVar_ID_61412 Human_SNP_ID_291274269 m1A Human chr6 + 108684385 108684385 108684385 AAAAAAATCTGTATACAGTATCTGTAAAAACTATCTTATCTGTTTCAATTCCTTGCTCATATCCC AAAAAAATCTGTATACAGTATCTGTAAAAACTGTCTTATCTGTTTCAATTCCTTGCTCATATCCC A G FOXO3 Ensembl:ENSG00000118689 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1062034 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_17309139 61413 RMVar_ID_61413 Human_SNP_ID_291319588 m1A Human chr6 + 108879318 108879318 108879318 ATCCATCTATCCATCCATCTACCCATCCACCCATCCATATATCTACCCATCTGTCTACCCATGCA ATCCATCTATCCATCCATCTACCCATCCACCCGTCCATATATCTACCCATCTGTCTACCCATGCA A G ARMC2 Ensembl:ENSG00000118690 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:108879273..108879418 26863196 MeRIP-seq:(Medium) rs1261621000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214644 RMVar_hsa_circ_4717,RMVar_hsa_circ_339073,RMVar_hsa_circ_378600,RMVar_hsa_circ_28061,RMVar_hsa_circ_72924,RMVar_hsa_circ_240778,RMVar_hsa_circ_240774,RMVar_hsa_circ_85781,RMVar_hsa_circ_240775,RMVar_hsa_circ_10313,RMVar_hsa_circ_296790,RMVar_hsa_circ_12370,RMVar_hsa_circ_315095,RMVar_hsa_circ_240777,RMVar_hsa_circ_327360,RMVar_hsa_circ_240779 61414 RMVar_ID_61414 Human_SNP_ID_291345637 m1A Human chr6 - 108992076 108992076 108992076 ATAAATAAGCTAAGGGGCAAAATTTAGGCACAAGGAAGAGTTATAGAATAATTATGCAATAGATT ATAAATAAGCTAAGGGGCAAAATTTAGGCACAGGGAAGAGTTATAGAATAATTATGCAATAGATT T C SESN1 Ensembl:ENSG00000080546 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:108991948..108992075 26863196 MeRIP-seq:(Medium) rs939560990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31340,RMVar_hsa_circ_344203,RMVar_hsa_circ_9766,RMVar_hsa_circ_240805 61415 RMVar_ID_61415 Human_SNP_ID_291432490 m1A Human chr6 + 109367609 109367609 109367609 ATACTATGGGAAACCAAGAAGGAAGGGAGAGAAAAAGAAAAAGCACAGTCTATTCATCCAGGACA ATACTATGGGAAACCAAGAAGGAAGGGAGAGAGAAAGAAAAAGCACAGTCTATTCATCCAGGACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:109367562..109367662 32194978 MeRIP-seq:(Medium) rs924931897 Functional Loss SNV dbSNP153 33..33 33 - - - 61416 RMVar_ID_61416 Human_SNP_ID_291434197 m1A Human chr6 + 109374004 109374004 109374004 TTCAAGATGAGTTGTCCTTGTTACAGCATTTGACTACTTCTTCCTTTGAAAAACTACGCCCACAA TTCAAGATGAGTTGTCCTTGTTACAGCATTTGCCTACTTCTTCCTTTGAAAAACTACGCCCACAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109374002..109374528 26863196 MeRIP-seq:(Medium) rs1416682143 Functional Loss SNV dbSNP153 33..33 33 - - - 61417 RMVar_ID_61417 Human_SNP_ID_291434207 m1A Human chr6 + 109374033 109374033 109374033 TTGACTACTTCTTCCTTTGAAAAACTACGCCCACAACCACATACTGTTAGTTTCTTGCACATACT TTGACTACTTCTTCCTTTGAAAAACTACGCCCGCAACCACATACTGTTAGTTTCTTGCACATACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:109374027..109374521 26863196 MeRIP-seq:(Medium) rs766128505 Functional Loss SNV dbSNP153 33..33 33 - - - 61418 RMVar_ID_61418 Human_SNP_ID_291436815 m1A Human chr6 + 109382261 109382261 109382261 GAGGGACGTCACCGGCGCCGAGGTTACGTTGGAGATGGGCGCTAAAGTCGTCACGTTCGGGTGCT GAGGGACGTCACCGGCGCCGAGGTTACGTTGGGGATGGGCGCTAAAGTCGTCACGTTCGGGTGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:109382201..109382425 32194978 MeRIP-seq:(Medium) rs11542732 Functional Loss SNV dbSNP153 33..33 33 - - - 61419 RMVar_ID_61419 Human_SNP_ID_291436821 m1A Human chr6 + 109382274 109382274 109382274 GGCGCCGAGGTTACGTTGGAGATGGGCGCTAAAGTCGTCACGTTCGGGTGCTGGGTCGTGTTCTT GGCGCCGAGGTTACGTTGGAGATGGGCGCTAACGTCGTCACGTTCGGGTGCTGGGTCGTGTTCTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:109382226..109382450 26863196 MeRIP-seq:(Medium) rs760727081 Functional Loss SNV dbSNP153 33..33 33 - - - 61420 RMVar_ID_61420 Human_SNP_ID_291436852 m1A Human chr6 + 109382324 109382324 109382324 CTGGGTCGTGTTCTTGTCCGCGGACAGCACGCAGAGCACGCCCAGGCAGGTGGCGGCCCAAAGCA CTGGGTCGTGTTCTTGTCCGCGGACAGCACGCCGAGCACGCCCAGGCAGGTGGCGGCCCAAAGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:109382273..109382450 26863196 MeRIP-seq:(Medium) rs749077551 Functional Loss SNV dbSNP153 33..33 33 - - - 61421 RMVar_ID_61421 Human_SNP_ID_291450623 m1A Human chr6 + 109440572 109440572 109440572 CGGCGAGCCGCACCTAGCGTGCGGGGGCCCGCACGGCTGCGGCCTTGCCATGGCCGCGCCCGGGG CGGCGAGCCGCACCTAGCGTGCGGGGGCCCGCCCGGCTGCGGCCTTGCCATGGCCGCGCCCGGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:109440473..109440574 26863196 MeRIP-seq:(Medium) rs1415992913 Functional Loss SNV dbSNP153 33..33 33 - - - 61422 RMVar_ID_61422 Human_SNP_ID_291452723 m1A Human chr6 - 109446227 109446227 109446227 AACCTTACCCCTGACCCGGAAATGGAGCCTCCACCCAAGCCTCCCCGCAGCTGCTCCGCCTTGGC AACCTTACCCCTGACCCGGAAATGGAGCCTCCGCCCAAGCCTCCCCGCAGCTGCTCCGCCTTGGC T C MICAL1 Ensembl:ENSG00000135596 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:109446178..109446427 32194978 MeRIP-seq:(Medium) rs752374975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_801111,Human_Splice_Rec_801157,Human_Splice_Rec_801205,Human_Splice_Rec_801221,Human_Splice_Rec_801269 RMVar_hsa_circ_23978,RMVar_hsa_circ_240832,RMVar_hsa_circ_79517,RMVar_hsa_circ_89014,RMVar_hsa_circ_96769,RMVar_hsa_circ_45094,RMVar_hsa_circ_240836,RMVar_hsa_circ_75062,RMVar_hsa_circ_240837 61423 RMVar_ID_61423 Human_SNP_ID_291454323 m1A Human chr6 + 109450010 109450010 109450010 CAACACCTCTAGGGACTCAGCGCCCTCTGCCCACCGCTTCACCATCCAGGCTGCATCAAAGGCTG CAACACCTCTAGGGACTCAGCGCCCTCTGCCCGCCGCTTCACCATCCAGGCTGCATCAAAGGCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109449934..109450009 26863196 MeRIP-seq:(Medium) rs1169762646 Functional Loss SNV dbSNP153 33..33 33 - - - 61424 RMVar_ID_61424 Human_SNP_ID_291456024 m1A Human chr6 - 109455286 109455286 109455286 TCTCCTGTCTCGGCGCGGCGGGCTGGGAACGGAGGGGCAGCTGGATGGTGGAGGGGCCTGAGCCT TCTCCTGTCTCGGCGCGGCGGGCTGGGAACGGGGGGGCAGCTGGATGGTGGAGGGGCCTGAGCCT T C MICAL1 Ensembl:ENSG00000135596 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:109455245..109455349 32194978 MeRIP-seq:(Medium) rs1327912375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240841,RMVar_hsa_circ_78095 61425 RMVar_ID_61425 Human_SNP_ID_291456135 m1A Human chr6 + 109455676 109455676 109455676 CGTTTCCCCGGAAGCGCACCCCACCTCACCCCACCCGGCCGCGGGGCTCGCAGCCGGCTCCGCTG CGTTTCCCCGGAAGCGCACCCCACCTCACCCCCCCCGGCCGCGGGGCTCGCAGCCGGCTCCGCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109455666..109455736 26863196 MeRIP-seq:(Medium) rs1419870506 Functional Loss SNV dbSNP153 33..33 33 - - - 61426 RMVar_ID_61426 Human_SNP_ID_291459170 m1A Human chr6 + 109468176 109468176 109468176 TATATCAACCTTCCAAATATATCCAGAATCTGACCACTGCTCAGTACCTCCACTGCCACTCTCTT TATATCAACCTTCCAAATATATCCAGAATCTGCCCACTGCTCAGTACCTCCACTGCCACTCTCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:109468128..109468239 26863196 MeRIP-seq:(Medium) rs964985188 Functional Loss SNV dbSNP153 33..33 33 - - - 61427 RMVar_ID_61427 Human_SNP_ID_291460192 m1A Human chr6 + 109472847 109472847 109472847 GGCTTTTGCCTCCTCTTTCAACTCCCACATCCAATCATGAGCGAATCACATGAATTCTTCCCTGG GGCTTTTGCCTCCTCTTTCAACTCCCACATCCCATCATGAGCGAATCACATGAATTCTTCCCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109472797..109472938 26863196 MeRIP-seq:(Medium) rs768219384 Functional Loss SNV dbSNP153 33..33 33 - - - 61428 RMVar_ID_61428 Human_SNP_ID_291462512 m1A Human chr6 - 109481425 109481425 109481425 TTCAGTTCAGAATAGACAAAACTTTGTGGTTAAAGGAGACAGTGGTGTACTGAATGAGCAAATTG TTCAGTTCAGAATAGACAAAACTTTGTGGTTACAGGAGACAGTGGTGTACTGAATGAGCAAATTG T G ZBTB24 Ensembl:ENSG00000112365 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109481376..109481456 26863196 MeRIP-seq:(Medium) rs1562304893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27086316 RMVar_hsa_circ_58153 61429 RMVar_ID_61429 Human_SNP_ID_291463022 m1A Human chr6 + 109483120 109483120 109483120 GCCAACTCACCCGGCGGCCTGGCGGGAGACCCACGCCGGGGCCCGCTGGCCCTCCGCTCCGCCCC GCCAACTCACCCGGCGGCCTGGCGGGAGACCCGCGCCGGGGCCCGCTGGCCCTCCGCTCCGCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:109483094..109483193 26863196 MeRIP-seq:(Medium) rs905084999 Functional Loss SNV dbSNP153 33..33 33 - - - 61430 RMVar_ID_61430 Human_SNP_ID_291463053 m1A Human chr6 - 109483171 109483171 109483171 CGGCGGCGCAGGAGCAGAAACCGGTGCGGCGCAGAAGCCCCAGAGGCGGGCGGGGCGGAGCGGAG CGGCGGCGCAGGAGCAGAAACCGGTGCGGCGCCGAAGCCCCAGAGGCGGGCGGGGCGGAGCGGAG T G ZBTB24 Ensembl:ENSG00000112365 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:109483070..109483199;chr6:109483122..109483206 26863196 MeRIP-seq:(Medium) rs1335155979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4905071 Human_Splice_Rec_801307 61431 RMVar_ID_61431 Human_SNP_ID_291523900 m1A Human chr6 - 109738782 109738782 109738782 GCTGCTAAGGCACTGACTTTTGTTTAGGGCCCAGGCCAAGTTCAACTATTCCCATGGGCCTGTCC GCTGCTAAGGCACTGACTTTTGTTTAGGGCCCGGGCCAAGTTCAACTATTCCCATGGGCCTGTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:109738731..109738821 26863196 MeRIP-seq:(Medium) rs1036203226 Functional Loss SNV dbSNP153 33..33 33 - - - 61432 RMVar_ID_61432 Human_SNP_ID_291610941 m1A Human chr6 - 110101713 110101713 110101713 ACATCCAACTCCATCTACTGCCCCAGGTCCCCATGTTCCATTAATGCCTCCATCTCCTCCATCAC ACATCCAACTCCATCTACTGCCCCAGGTCCCCGTGTTCCATTAATGCCTCCATCTCCTCCATCAC T C WASF1 Ensembl:ENSG00000112290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:110101664..110101825 26863196 MeRIP-seq:(Medium) rs546806345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134376,Human_RBP_ID_9185521,Human_RBP_ID_17309970,Human_RBP_ID_23053167 RMVar_hsa_circ_39421,RMVar_hsa_circ_240886 61433 RMVar_ID_61433 Human_SNP_ID_291611086 m1A Human chr6 - 110102149 110102149 110102149 CACCAGCTACAGGCAGAACACCTGTGTTTGTGAGCCCCACTCCCCCACCTCCTCCACCACCTCTT CACCAGCTACAGGCAGAACACCTGTGTTTGTGCGCCCCACTCCCCCACCTCCTCCACCACCTCTT T G WASF1 Ensembl:ENSG00000112290 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:110101926..110102148 26863196 MeRIP-seq:(Medium) rs991226887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18958584 Human_Splice_Rec_801680,Human_Splice_Rec_801696,Human_Splice_Rec_801716,Human_Splice_Rec_801734,Human_Splice_Rec_801752 Human_miRNA_ID_96850,Human_miRNA_ID_1322542,Human_miRNA_ID_1479138 RMVar_hsa_circ_39421 61434 RMVar_ID_61434 Human_SNP_ID_291762722 m1A Human chr6 - 110746201 110746201 110746201 TGGAAAAATGATGTTTTTTTGTTTATGTGCAGAAAAGATGAAAAGGAATATGCATTGAAGCAAAT TGGAAAAATGATGTTTTTTTGTTTATGTGCAGCAAAGATGAAAAGGAATATGCATTGAAGCAAAT T G CDK19 Ensembl:ENSG00000155111 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:110746156..110813202;chr6:110746156..110773931 26863196 MeRIP-seq:(Medium) rs765991784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949971 Human_Splice_Rec_802036,Human_Splice_Rec_802037,Human_Splice_Rec_802058,Human_Splice_Rec_802059,Human_Splice_Rec_802084,Human_Splice_Rec_802085,Human_Splice_Rec_802110,Human_Splice_Rec_802111,Human_Splice_Rec_802125 RMVar_hsa_circ_54241,RMVar_hsa_circ_5890,RMVar_hsa_circ_100945,RMVar_hsa_circ_240902,RMVar_hsa_circ_50434,RMVar_hsa_circ_78429,RMVar_hsa_circ_240905,RMVar_hsa_circ_318766,RMVar_hsa_circ_18043,RMVar_hsa_circ_55201,RMVar_hsa_circ_371744,RMVar_hsa_circ_240912,RMVar_hsa_circ_271630,RMVar_hsa_circ_280451,RMVar_hsa_circ_240916,RMVar_hsa_circ_240917,RMVar_hsa_circ_240919,RMVar_hsa_circ_240921,RMVar_hsa_circ_240922,RMVar_hsa_circ_292863,RMVar_hsa_circ_240920,RMVar_hsa_circ_240918 61435 RMVar_ID_61435 Human_SNP_ID_291779643 m1A Human chr6 + 110814728 110814728 110814728 ACAAACTCCTCCTCCACCGCGGTCCCAACTCGAGTCCCCCCGCCGTCTCCGAGCACTCGGAGGGC ACAAACTCCTCCTCCACCGCGGTCCCAACTCGGGTCCCCCCGCCGTCTCCGAGCACTCGGAGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:110814677..110814822 32194978 MeRIP-seq:(Medium) rs899442396 Functional Loss SNV dbSNP153 33..33 33 - - - 61436 RMVar_ID_61436 Human_SNP_ID_291779979 m1A Human chr6 - 110815283 110815283 110815283 GTGGCCGCCGAGGAGTCCCTTGCTGAAGGCGGACCGCGGAGCGGCGGGCGGCGGGCGGCGCGCGC GTGGCCGCCGAGGAGTCCCTTGCTGAAGGCGGGCCGCGGAGCGGCGGGCGGCGGGCGGCGCGCGC T C CDK19 Ensembl:ENSG00000155111 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:110815025..110815588 26863196 MeRIP-seq:(Medium) rs1302320647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949972,Human_RBP_ID_3820906,Human_RBP_ID_5151964,Human_RBP_ID_5327207,Human_RBP_ID_8944032,Human_RBP_ID_9336754,Human_RBP_ID_18425711,Human_RBP_ID_23067875,Human_RBP_ID_23120295,Human_RBP_ID_26771777,Human_RBP_ID_26792503 61437 RMVar_ID_61437 Human_SNP_ID_291800121 m1A Human chr6 + 110892948 110892948 110892948 TATTGGACTATTCACATCACTCCAGAACCAGAATTTTCTTATGTTAGCTTTGAAACAAACTTAAG TATTGGACTATTCACATCACTCCAGAACCAGAGTTTTCTTATGTTAGCTTTGAAACAAACTTAAG A G AMD1 Ensembl:ENSG00000123505 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:110892815..110893011 32194978 MeRIP-seq:(Medium) rs1450346283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1661970,Human_RBP_ID_2004737,Human_RBP_ID_5399907,Human_RBP_ID_7519189,Human_RBP_ID_8627501,Human_RBP_ID_8895261,Human_RBP_ID_15602918,Human_RBP_ID_18851570,Human_RBP_ID_19134009,Human_RBP_ID_22619012,Human_RBP_ID_26038579,Human_RBP_ID_27086468 Human_Splice_Rec_802150,Human_Splice_Rec_802166,Human_Splice_Rec_802180,Human_Splice_Rec_802196,Human_Splice_Rec_802212,Human_Splice_Rec_802228,Human_Splice_Rec_802238,Human_Splice_Rec_802244,Human_Splice_Rec_802248 RMVar_hsa_circ_36859,RMVar_hsa_circ_112997,RMVar_hsa_circ_240925,RMVar_hsa_circ_68921,RMVar_hsa_circ_240930,RMVar_hsa_circ_33037,RMVar_hsa_circ_95601,RMVar_hsa_circ_124187,RMVar_hsa_circ_240932,RMVar_hsa_circ_240934,RMVar_hsa_circ_240933,RMVar_hsa_circ_340380 61438 RMVar_ID_61438 Human_SNP_ID_291800522 m1A Human chr6 - 110894527 110894527 110894527 ACTCATTAGACGCTAATCTCATTTACTGAGGAACACAGAATTGTATGTTTTCCACAGTTCAGCCA ACTCATTAGACGCTAATCTCATTTACTGAGGAGCACAGAATTGTATGTTTTCCACAGTTCAGCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:110894317..110894617 32194978 MeRIP-seq:(Medium) rs1368459689 Functional Loss SNV dbSNP153 33..33 33 - - - 61439 RMVar_ID_61439 Human_SNP_ID_291808173 m1A Human chr6 + 110923678 110923678 110923678 GCTGCAGTCTGAGAAGCAGAAGGCCAGGGAAGAAGAGGAGCAAAAAGAAGGTGGAGACGGGGCTG GCTGCAGTCTGAGAAGCAGAAGGCCAGGGAAGTAGAGGAGCAAAAAGAAGGTGGAGACGGGGCTG A T AL357515.1 Ensembl:ENSG00000219329 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:110923624..110923716 26863196 MeRIP-seq:(Medium) rs533052065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5104220,Human_RBP_ID_17422530 61440 RMVar_ID_61440 Human_SNP_ID_291816840 m1A Human chr6 - 110958735 110958735 110958735 TCCCGCGGCGCCTCGCCTTCTAGTCACTGGCCACGCCCGCCCGGAGCCGCCATCTTGAGTACGGG TCCCGCGGCGCCTCGCCTTCTAGTCACTGGCCGCGCCCGCCCGGAGCCGCCATCTTGAGTACGGG T C lnc-CDK19-6 RNACentral:URS0000D59297 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:110958704..110958848 26863196 MeRIP-seq:(Medium) rs766271471 Functional Loss SNV dbSNP153 33..33 33 - - - 61441 RMVar_ID_61441 Human_SNP_ID_291816841 m1A Human chr6 - 110958735 110958735 110958735 TCCCGCGGCGCCTCGCCTTCTAGTCACTGGCCACGCCCGCCCGGAGCCGCCATCTTGAGTACGGG TCCCGCGGCGCCTCGCCTTCTAGTCACTGGCCCCGCCCGCCCGGAGCCGCCATCTTGAGTACGGG T G lnc-CDK19-6 RNACentral:URS0000D59297 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:110958704..110958848 26863196 MeRIP-seq:(Medium) rs766271471 Functional Loss SNV dbSNP153 33..33 33 - - - 61442 RMVar_ID_61442 Human_SNP_ID_291816872 m1A Human chr6 + 110958767 110958767 110958767 TGGCCAGTGACTAGAAGGCGAGGCGCCGCGGGACCATGGCGGCGGCGGCGGACGAGCGGAGTCCA TGGCCAGTGACTAGAAGGCGAGGCGCCGCGGGCCCATGGCGGCGGCGGCGGACGAGCGGAGTCCA A C GTF3C6 Ensembl:ENSG00000155115 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:110958717..110958871 26863196 MeRIP-seq:(Medium) rs772749014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13526,Human_RBP_ID_4860514,Human_RBP_ID_9400997,Human_RBP_ID_23067619,Human_RBP_ID_26354316,Human_RBP_ID_27086491 Human_Splice_Rec_802251 61443 RMVar_ID_61443 Human_SNP_ID_291816902 m1A Human chr6 - 110958796 110958796 110958796 ACCTCCTCTTCCTCGTCTTCTCCGTCCTCTGGACTCCGCTCGTCCGCCGCCGCCGCCATGGTCCC ACCTCCTCTTCCTCGTCTTCTCCGTCCTCTGGTCTCCGCTCGTCCGCCGCCGCCGCCATGGTCCC T A lnc-CDK19-6 RNACentral:URS0000D59297 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:110958524..110958952;chr6:110958568..110958952;chr6:110958549..110958891 26863196 MeRIP-seq:(Medium) rs1301099593 Functional Loss SNV dbSNP153 33..33 33 - - - 61444 RMVar_ID_61444 Human_SNP_ID_291816903 m1A Human chr6 - 110958796 110958796 110958796 ACCTCCTCTTCCTCGTCTTCTCCGTCCTCTGGACTCCGCTCGTCCGCCGCCGCCGCCATGGTCCC ACCTCCTCTTCCTCGTCTTCTCCGTCCTCTGGCCTCCGCTCGTCCGCCGCCGCCGCCATGGTCCC T G lnc-CDK19-6 RNACentral:URS0000D59297 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:110958524..110958952;chr6:110958568..110958952;chr6:110958549..110958891 26863196 MeRIP-seq:(Medium) rs1301099593 Functional Loss SNV dbSNP153 33..33 33 - - - 61445 RMVar_ID_61445 Human_SNP_ID_291817503 m1A Human chr6 + 110960579 110960579 110960579 AATTTGCCTTTGTATTTTTCTGCAGACACTCTAGGGACCTGTGTTATATTTGAAGAAAATGTTGA AATTTGCCTTTGTATTTTTCTGCAGACACTCTGGGGACCTGTGTTATATTTGAAGAAAATGTTGA A G GTF3C6 Ensembl:ENSG00000155115 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:110960401..110960625 26863196 MeRIP-seq:(Medium) rs574625046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2004786,Human_RBP_ID_9401001,Human_RBP_ID_15603288,Human_RBP_ID_24128920,Human_RBP_ID_27828855 Human_Splice_Rec_802256,Human_Splice_Rec_802257,Human_Splice_Rec_802266,Human_Splice_Rec_802267 Human_miRNA_ID_2582899 RMVar_hsa_circ_240935,RMVar_hsa_circ_303242,RMVar_hsa_circ_304599 61446 RMVar_ID_61446 Human_SNP_ID_291819311 m1A Human chr6 - 110967462 110967462 110967462 TGAGGAATAAACAAAAAAAGAAACAAAAAATGAATTTTAGTATATTTTTCTTTAATTTAAATTTC TGAGGAATAAACAAAAAAAGAAACAAAAAATGTATTTTAGTATATTTTTCTTTAATTTAAATTTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:110967458..110967599 26863196 MeRIP-seq:(Medium) rs139531098 Functional Loss SNV dbSNP153 33..33 33 - - - 61447 RMVar_ID_61447 Human_SNP_ID_291819312 m1A Human chr6 - 110967462 110967462 110967462 TGAGGAATAAACAAAAAAAGAAACAAAAAATGAATTTTAGTATATTTTTCTTTAATTTAAATTTC TGAGGAATAAACAAAAAAAGAAACAAAAAATGCATTTTAGTATATTTTTCTTTAATTTAAATTTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:110967458..110967599 26863196 MeRIP-seq:(Medium) rs139531098 Functional Loss SNV dbSNP153 33..33 33 - - - 61448 RMVar_ID_61448 Human_SNP_ID_291823111 m1A Human chr6 - 110982079 110982078 110982079 TCCATCGCTACCGCTACCTGCAACTCTTAACCAGGGGGCATGCACGTGCCCTCGGCGATTACGTG TCCATCGCTACCGCTACCTGCAACTCTTAACC_GGGGGCATGCACGTGCCCTCGGCGATTACGTG CT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:110982050..110982192 26863196 MeRIP-seq:(Medium) rs772814863 Functional Loss DEL dbSNP153 33..33 33 - - - 61449 RMVar_ID_61449 Human_SNP_ID_291823113 m1A Human chr6 - 110982079 110982079 110982079 TCCATCGCTACCGCTACCTGCAACTCTTAACCAGGGGGCATGCACGTGCCCTCGGCGATTACGTG TCCATCGCTACCGCTACCTGCAACTCTTAACCCGGGGGCATGCACGTGCCCTCGGCGATTACGTG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:110982050..110982192 26863196 MeRIP-seq:(Medium) rs746470504 Functional Loss SNV dbSNP153 33..33 33 - - - 61450 RMVar_ID_61450 Human_SNP_ID_291823132 m1A Human chr6 - 110982102 110982102 110982102 CTTACACTACTCGATCCAGAGTGTCCATCGCTACCGCTACCTGCAACTCTTAACCAGGGGGCATG CTTACACTACTCGATCCAGAGTGTCCATCGCTGCCGCTACCTGCAACTCTTAACCAGGGGGCATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:110982051..110982178 26863196 MeRIP-seq:(Medium) rs1267551619 Functional Loss SNV dbSNP153 33..33 33 - - - 61451 RMVar_ID_61451 Human_SNP_ID_291823152 m1A Human chr6 - 110982129 110982129 110982129 CGCTCCCCGGGGCTGAGACCCAGCGCACTTACACTACTCGATCCAGAGTGTCCATCGCTACCGCT CGCTCCCCGGGGCTGAGACCCAGCGCACTTACCCTACTCGATCCAGAGTGTCCATCGCTACCGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:110982099..110982190;chr6:110982100..110982190 26863196 MeRIP-seq:(Medium) rs1213988791 Functional Loss SNV dbSNP153 33..33 33 - - - 61452 RMVar_ID_61452 Human_SNP_ID_291849235 m1A Human chr6 - 111087545 111087545 111087545 GAGGACAGCTGGCGCGCGCGAACACCTCGGGGATCGACACTGAAGCCTCTAGGTCACAGCCCCGC GAGGACAGCTGGCGCGCGCGAACACCTCGGGGGTCGACACTGAAGCCTCTAGGTCACAGCCCCGC T C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111087499..111087703 26863196 MeRIP-seq:(Medium) rs1489761548 Functional Loss SNV dbSNP153 33..33 33 - - - 61453 RMVar_ID_61453 Human_SNP_ID_291849239 m1A Human chr6 - 111087557 111087557 111087557 GCAGGCGGCCGCGAGGACAGCTGGCGCGCGCGAACACCTCGGGGATCGACACTGAAGCCTCTAGG GCAGGCGGCCGCGAGGACAGCTGGCGCGCGCGGACACCTCGGGGATCGACACTGAAGCCTCTAGG T C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:111087507..111087678 26863196 MeRIP-seq:(Medium) rs1249153396 Functional Loss SNV dbSNP153 33..33 33 - - - 61454 RMVar_ID_61454 Human_SNP_ID_291849244 m1A Human chr6 - 111087576 111087576 111087576 GCGCGCAGGCGGCCAGCGCGCAGGCGGCCGCGAGGACAGCTGGCGCGCGCGAACACCTCGGGGAT GCGCGCAGGCGGCCAGCGCGCAGGCGGCCGCGGGGACAGCTGGCGCGCGCGAACACCTCGGGGAT T C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:111087536..111087678 26863196 MeRIP-seq:(Medium) rs1403506331 Functional Loss SNV dbSNP153 33..33 33 - - - 61455 RMVar_ID_61455 Human_SNP_ID_291849397 m1A Human chr6 - 111087985 111087968 111087985 TCTGGATGCCGAACACCGACCCGTTGCACCACATGGCCGCCAGCATCACCAGCCAGCCCCAGCCG TCTGGATGCCGAACACCGACCCGTTGCACCAC_________________CAGCCAGCCCCAGCCG GGTGATGCTGGCGGCCAT G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:111087524..111088052 26863196 MeRIP-seq:(Medium) rs1269647834 Functional Loss DEL dbSNP153 33..49 33 - - - 61456 RMVar_ID_61456 Human_SNP_ID_291849397 m1A Human chr6 + 111087984 111087968 111087985 GCGGCTGGGGCTGGCTGGTGATGCTGGCGGCCATGTGGTGCAACGGGTCGGTGTTCGGCATCCAG GCGGCTGGGGCTGGCTG_________________GTGGTGCAACGGGTCGGTGTTCGGCATCCAG GGTGATGCTGGCGGCCAT G SLC16A10 Ensembl:ENSG00000112394 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:111087822..111088055 26863196 MeRIP-seq:(Medium) rs1269647834 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_651020,Human_RBP_ID_4905076 61457 RMVar_ID_61457 Human_SNP_ID_291849403 m1A Human chr6 - 111087985 111087985 111087985 TCTGGATGCCGAACACCGACCCGTTGCACCACATGGCCGCCAGCATCACCAGCCAGCCCCAGCCG TCTGGATGCCGAACACCGACCCGTTGCACCACTTGGCCGCCAGCATCACCAGCCAGCCCCAGCCG T A RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:111087524..111088052 26863196 MeRIP-seq:(Medium) rs772346861 Functional Loss SNV dbSNP153 33..33 33 - - - 61458 RMVar_ID_61458 Human_SNP_ID_291849404 m1A Human chr6 - 111087985 111087985 111087985 TCTGGATGCCGAACACCGACCCGTTGCACCACATGGCCGCCAGCATCACCAGCCAGCCCCAGCCG TCTGGATGCCGAACACCGACCCGTTGCACCACGTGGCCGCCAGCATCACCAGCCAGCCCCAGCCG T C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:111087524..111088052 26863196 MeRIP-seq:(Medium) rs772346861 Functional Loss SNV dbSNP153 33..33 33 - - - 61459 RMVar_ID_61459 Human_SNP_ID_291900467 m1A Human chr6 + 111306364 111306364 111306364 GACCTAAGAGAAGTTCAATATGGTATGGGTCGAGGTAGAGTGTGACAGAGAAGAGCAAGAAATCG GACCTAAGAGAAGTTCAATATGGTATGGGTCGTGGTAGAGTGTGACAGAGAAGAGCAAGAAATCG A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111306313..111306419 26863196 MeRIP-seq:(Medium) rs1025085672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15606227 61460 RMVar_ID_61460 Human_SNP_ID_291900477 m1A Human chr6 + 111306383 111306383 111306383 ATGGTATGGGTCGAGGTAGAGTGTGACAGAGAAGAGCAAGAAATCGTGACAGAGGGATAGCAGGT ATGGTATGGGTCGAGGTAGAGTGTGACAGAGATGAGCAAGAAATCGTGACAGAGGGATAGCAGGT A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:111306264..111306430 26863196 MeRIP-seq:(Medium) rs1164261147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15606227 61461 RMVar_ID_61461 Human_SNP_ID_291943864 m1A Human chr6 - 111482890 111482890 111482890 CCAGTGAAGGGAGGCAGTGGCGGCGGCGGCGAACATGTTTTCAGTAAGGATAGTGACTGCAGACT CCAGTGAAGGGAGGCAGTGGCGGCGGCGGCGAGCATGTTTTCAGTAAGGATAGTGACTGCAGACT T C REV3L Ensembl:ENSG00000009413 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:111482844..111483197 26863196 MeRIP-seq:(Medium) rs779418990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4906440,Human_RBP_ID_5401121,Human_RBP_ID_9336756 RMVar_hsa_circ_77645,RMVar_hsa_circ_240969,RMVar_hsa_circ_93025,RMVar_hsa_circ_240981 61462 RMVar_ID_61462 Human_SNP_ID_291943894 m1A Human chr6 + 111482932 111482932 111482932 CCGCCACTGCCTCCCTTCACTGGCGACCCGGCAGCGGCAGCAGCAGCGGCGGCGGCTCCCTCCGC CCGCCACTGCCTCCCTTCACTGGCGACCCGGCGGCGGCAGCAGCAGCGGCGGCGGCTCCCTCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:111482882..111483037 26863196 MeRIP-seq:(Medium) rs778105723 Functional Loss SNV dbSNP153 33..33 33 - - - 61463 RMVar_ID_61463 Human_SNP_ID_291961858 m1A Human chr6 + 111561477 111561477 111561477 AACAACCAAAAGAGGTGTCGGGGAGGCTAGAGAGATTGGGTGATATAAGGGTAAGTAAGAGTTCA AACAACCAAAAGAGGTGTCGGGGAGGCTAGAGGGATTGGGTGATATAAGGGTAAGTAAGAGTTCA A G TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111561464..111561594 26863196 MeRIP-seq:(Medium) rs1239020983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7521460 61464 RMVar_ID_61464 Human_SNP_ID_291971794 m1A Human chr6 + 111605706 111605706 111605706 GTAGAGGCAGAATGTTTCAGTAAAGGAGAAACAGCGTGCTTTGGGAAATAGGTCAGAGGTGAAGA GTAGAGGCAGAATGTTTCAGTAAAGGAGAAACGGCGTGCTTTGGGAAATAGGTCAGAGGTGAAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111605704..111605906 26863196 MeRIP-seq:(Medium) rs7769061 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7583,GWAS_ID_7584 61465 RMVar_ID_61465 Human_SNP_ID_292033055 m1A Human chr6 + 111872933 111872933 111872933 GCCGGCGGCCGGGCTTCTCCGCAGCATCCCCGAGGCCTCCCGCGACGCATCCCCGCCGCCTGCTT GCCGGCGGCCGGGCTTCTCCGCAGCATCCCCGTGGCCTCCCGCGACGCATCCCCGCCGCCTGCTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111872927..111873128 26863196 MeRIP-seq:(Medium) rs1003299776 Functional Loss SNV dbSNP153 33..33 33 - - - 61466 RMVar_ID_61466 Human_SNP_ID_292033246 m1A Human chr6 - 111873425 111873425 111873425 GGGGCAGAGCATCAGCAAGAGTAGCAGCGAGCAGCCGCGCTGGTGGCGGCGGCGCGTCGTTGCAG GGGGCAGAGCATCAGCAAGAGTAGCAGCGAGCGGCCGCGCTGGTGGCGGCGGCGCGTCGTTGCAG T C FYN Ensembl:ENSG00000010810 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:111873339..111873447 26863410 MeRIP-seq:(Medium) rs1460937471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266614 61467 RMVar_ID_61467 Human_SNP_ID_292084612 m1A Human chr6 - 112087437 112087437 112087437 GGCTAGCAAGCTCCCGGAGCCGGCGGCGCACCACCATGACCCAGTCGGTGGTCGTACAGGGTAAG GGCTAGCAAGCTCCCGGAGCCGGCGGCGCACCGCCATGACCCAGTCGGTGGTCGTACAGGGTAAG T C TUBE1 Ensembl:ENSG00000074935 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:112087339..112087436 26863196 MeRIP-seq:(Medium) rs1046680469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_651197,Human_RBP_ID_19019001 Human_Splice_Rec_803453,Human_Splice_Rec_803493,Human_Splice_Rec_803517,Human_Splice_Rec_803541,Human_Splice_Rec_803553,Human_Splice_Rec_803563,Human_Splice_Rec_803569 RMVar_hsa_circ_92466,RMVar_hsa_circ_241032 61468 RMVar_ID_61468 Human_SNP_ID_292087198 m1A Human chr6 - 112099376 112099376 112099376 CTGGTTGGTGACATCTCCTTCCCATTACAGGCAGCACTGGAGCTCAGCCCAGGTTCCAGCTCAAT CTGGTTGGTGACATCTCCTTCCCATTACAGGCGGCACTGGAGCTCAGCCCAGGTTCCAGCTCAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:112099326..112099425 32194978 MeRIP-seq:(Medium) rs1451440714 Functional Loss SNV dbSNP153 33..33 33 - - - 61469 RMVar_ID_61469 Human_SNP_ID_292520503 m1A Human chr6 - 113857613 113857609 113857613 GCAACAGCGGCAGCGGCACACACACCGGAGGGAGGGGGGTGGGGGTGGTGGAGAGGACAGAACAG GCAACAGCGGCAGCGGCACACACACCGGAGGG____GGGTGGGGGTGGTGGAGAGGACAGAACAG CCCCT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:113857460..113857660 32194978 MeRIP-seq:(Medium) rs1334420038 Functional Loss DEL dbSNP153 33..36 33 - - - 61470 RMVar_ID_61470 Human_SNP_ID_292520508 m1A Human chr6 - 113857613 113857613 113857613 GCAACAGCGGCAGCGGCACACACACCGGAGGGAGGGGGGTGGGGGTGGTGGAGAGGACAGAACAG GCAACAGCGGCAGCGGCACACACACCGGAGGGGGGGGGGTGGGGGTGGTGGAGAGGACAGAACAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:113857460..113857660 32194978 MeRIP-seq:(Medium) rs1471192989 Functional Loss SNV dbSNP153 33..33 33 - - - 61471 RMVar_ID_61471 Human_SNP_ID_292520535 m1A Human chr6 - 113857661 113857661 113857661 CCTCGGGTTGGTGTAACGACGGGGCGAGCAGCAGCAGCAGCGGCGGCGGCAACAGCGGCAGCGGC CCTCGGGTTGGTGTAACGACGGGGCGAGCAGCCGCAGCAGCGGCGGCGGCAACAGCGGCAGCGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:113857387..113857915 26863196 MeRIP-seq:(Medium) rs1347751322 Functional Loss SNV dbSNP153 33..33 33 - - - 61472 RMVar_ID_61472 Human_SNP_ID_292520557 m1A Human chr6 - 113857720 113857720 113857720 CACCCATGCTGGCTTCTTCAACAAAGAAACTCAACAGATCCAAGAGGGGAAACAAAGAGCCTCGG CACCCATGCTGGCTTCTTCAACAAAGAAACTCTACAGATCCAAGAGGGGAAACAAAGAGCCTCGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:113857560..113860600 32194978 MeRIP-seq:(Medium) rs368150133 Functional Loss SNV dbSNP153 33..33 33 - - - 61473 RMVar_ID_61473 Human_SNP_ID_292521366 m1A Human chr6 + 113860007 113860007 113860007 CGACTTCTTCGCCCAAGGCCGAGGACGGGGCCACGCCCTCGCCCAGCAACGAGACCCCGAAAAAA CGACTTCTTCGCCCAAGGCCGAGGACGGGGCCGCGCCCTCGCCCAGCAACGAGACCCCGAAAAAA A G MARCKS Ensembl:ENSG00000277443 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:113859762..113860050 26863196 MeRIP-seq:(Medium) rs754671406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789524,Human_RBP_ID_951405,Human_RBP_ID_22462176 61474 RMVar_ID_61474 Human_SNP_ID_292521425 m1A Human chr6 + 113860134 113860134 113860134 CAAGAAGGAGGCTGGAGAAGGCGGTGAGGCTGAGGCGCCCGCTGCCGAAGGCGGCAAGGACGAGG CAAGAAGGAGGCTGGAGAAGGCGGTGAGGCTGGGGCGCCCGCTGCCGAAGGCGGCAAGGACGAGG A G MARCKS Ensembl:ENSG00000277443 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:113860091..113860522;chr6:113859673..113860650;chr6:113857351..113860650;chr6:113857351..113860700 26863196 MeRIP-seq:(Medium) rs767199531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841529,Human_RBP_ID_951406,Human_RBP_ID_7523306,Human_RBP_ID_15614708,Human_RBP_ID_18061281,Human_RBP_ID_22106898,Human_RBP_ID_22461388 61475 RMVar_ID_61475 Human_SNP_ID_292521435 m1A Human chr6 + 113860150 113860150 113860150 GAAGGCGGTGAGGCTGAGGCGCCCGCTGCCGAAGGCGGCAAGGACGAGGCCGCCGGGGGCGCAGC GAAGGCGGTGAGGCTGAGGCGCCCGCTGCCGACGGCGGCAAGGACGAGGCCGCCGGGGGCGCAGC A C MARCKS Ensembl:ENSG00000277443 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:113860101..113860522 26863196 MeRIP-seq:(Medium) rs753655112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951406,Human_RBP_ID_7523309,Human_RBP_ID_22106898,Human_RBP_ID_22461388 61476 RMVar_ID_61476 Human_SNP_ID_292521474 m1A Human chr6 + 113860249 113860232 113860250 GAGCAGGCAGCGGCGCCGGGCGAGGAGGCGGCAGCGGGCGAGGAGGGGGCGGCGGGTGGCGACCC GAGCAGGCAGCGGCGC__________________CGGGCGAGGAGGGGGCGGCGGGTGGCGACCC CCGGGCGAGGAGGCGGCAG C MARCKS Ensembl:ENSG00000277443 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:113860132..113860300 26863196 MeRIP-seq:(Medium) rs1325571001 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_251846,Human_RBP_ID_789525,Human_RBP_ID_7523310,Human_RBP_ID_22461389 61477 RMVar_ID_61477 Human_SNP_ID_292521479 m1A Human chr6 + 113860239 113860239 113860239 GGCCTCCGGGGAGCAGGCAGCGGCGCCGGGCGAGGAGGCGGCAGCGGGCGAGGAGGGGGCGGCGG GGCCTCCGGGGAGCAGGCAGCGGCGCCGGGCGTGGAGGCGGCAGCGGGCGAGGAGGGGGCGGCGG A T MARCKS Ensembl:ENSG00000277443 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Starvation treatment;HTR8/Svneo,Normoxia chr6:113860152..113860238;chr6:113860140..113860290 26863410,32194978 MeRIP-seq:(Medium) rs1016230776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789525,Human_RBP_ID_18472124,Human_RBP_ID_22461388 61478 RMVar_ID_61478 Human_SNP_ID_292521625 m1A Human chr6 - 113860502 113860502 113860502 CTGGGCCTCCTGTGAGGGGGCTGCGCAGGCTGACGAGGCTGCGGCGGCCGCGGGCTCCTCCGCGG CTGGGCCTCCTGTGAGGGGGCTGCGCAGGCTGGCGAGGCTGCGGCGGCCGCGGGCTCCTCCGCGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:113860420..113860539 26863196 MeRIP-seq:(Medium) rs1188670141 Functional Loss SNV dbSNP153 33..33 33 - - - 61479 RMVar_ID_61479 Human_SNP_ID_292541039 m1A Human chr6 - 113939129 113939129 113939129 GAGATCCTGGAGTAGTGGATGGAGGAGATGGAACAGTGAAGACGGAAACTGAGCTCAGTATCCGG GAGATCCTGGAGTAGTGGATGGAGGAGATGGAGCAGTGAAGACGGAAACTGAGCTCAGTATCCGG T C HDAC2 Ensembl:ENSG00000196591 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:113939079..113939267 26863196 MeRIP-seq:(Medium) rs1168365581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_651336,Human_RBP_ID_7523571,Human_RBP_ID_15615337 61480 RMVar_ID_61480 Human_SNP_ID_292549128 m1A Human chr6 + 113971020 113971020 113971020 GAGAGAAAAGGGCTGAGGGAAACGTGGGGGCGATAGTCCCGCGGGGAAGGGCAGGCCGGTGGGAG GAGAGAAAAGGGCTGAGGGAAACGTGGGGGCGCTAGTCCCGCGGGGAAGGGCAGGCCGGTGGGAG A C HDAC2-AS2 Ensembl:ENSG00000228624 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:113970876..113971150 26863196 MeRIP-seq:(Medium) rs1367603116 Functional Loss SNV dbSNP153 33..33 33 - - - 61481 RMVar_ID_61481 Human_SNP_ID_292549130 m1A Human chr6 + 113971022 113971022 113971022 GAGAAAAGGGCTGAGGGAAACGTGGGGGCGATAGTCCCGCGGGGAAGGGCAGGCCGGTGGGAGGA GAGAAAAGGGCTGAGGGAAACGTGGGGGCGATCGTCCCGCGGGGAAGGGCAGGCCGGTGGGAGGA A C HDAC2-AS2 Ensembl:ENSG00000228624 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:113970935..113971107 26863196 MeRIP-seq:(Medium) rs750440472 Functional Loss SNV dbSNP153 33..33 33 - - - 61482 RMVar_ID_61482 Human_SNP_ID_292549131 m1A Human chr6 + 113971022 113971022 113971022 GAGAAAAGGGCTGAGGGAAACGTGGGGGCGATAGTCCCGCGGGGAAGGGCAGGCCGGTGGGAGGA GAGAAAAGGGCTGAGGGAAACGTGGGGGCGATGGTCCCGCGGGGAAGGGCAGGCCGGTGGGAGGA A G HDAC2-AS2 Ensembl:ENSG00000228624 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:113970935..113971107 26863196 MeRIP-seq:(Medium) rs750440472 Functional Loss SNV dbSNP153 33..33 33 - - - 61483 RMVar_ID_61483 Human_SNP_ID_292549195 m1A Human chr6 - 113971120 113971120 113971120 TGGCCCCCTCCTCGCGAGTTGGTGCCGCTGCCACCTCCGATTCCGAGCTTTCGGCACCTCTGCCG TGGCCCCCTCCTCGCGAGTTGGTGCCGCTGCCGCCTCCGATTCCGAGCTTTCGGCACCTCTGCCG T C HDAC2 Ensembl:ENSG00000196591 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:113971026..113971150 26863410 MeRIP-seq:(Medium) rs374558098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903474,Human_RBP_ID_5450366 61484 RMVar_ID_61484 Human_SNP_ID_293071800 m1A Human chr6 - 116100908 116100908 116100908 GCTGAGCCATGGCTGCGCGGGGAGCACCAGGGAGCGCCTCGGCCGCGAAGGGTGCAAGGAGCTGG GCTGAGCCATGGCTGCGCGGGGAGCACCAGGGGGCGCCTCGGCCGCGAAGGGTGCAAGGAGCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:116100860..116100955 26863196 MeRIP-seq:(Medium) rs761859844 Functional Loss SNV dbSNP153 33..33 33 - - - 61485 RMVar_ID_61485 Human_SNP_ID_293108295 m1A Human chr6 - 116253464 116253455 116253464 GGCGATGGAGGAAAAGAAGGTAGTGCAGAAGGAAAAAAAGGTGGCAGGAGGGGTGAAAGAGGAGA GGCGATGGAGGAAAAGAAGGTAGTGCAGAAGG_________TGGCAGGAGGGGTGAAAGAGGAGA ACCTTTTTTT A TSPYL4 Ensembl:ENSG00000187189 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:116253415..116253564 26863196 MeRIP-seq:(Medium) rs1355318577 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_17069811,Human_RBP_ID_21991807,Human_RBP_ID_22106903 61486 RMVar_ID_61486 Human_SNP_ID_293108302 m1A Human chr6 - 116253464 116253464 116253464 GGCGATGGAGGAAAAGAAGGTAGTGCAGAAGGAAAAAAAGGTGGCAGGAGGGGTGAAAGAGGAGA GGCGATGGAGGAAAAGAAGGTAGTGCAGAAGGGAAAAAAGGTGGCAGGAGGGGTGAAAGAGGAGA T C TSPYL4 Ensembl:ENSG00000187189 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:116253415..116253564 26863196 MeRIP-seq:(Medium) rs1284929494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17069811,Human_RBP_ID_21991807,Human_RBP_ID_22106903 61487 RMVar_ID_61487 Human_SNP_ID_293108538 m1A Human chr6 - 116253934 116253934 116253934 ACCGGCGGCCTGGCTGCTCCCGACCATGCCTCAGGAGATCCGGACCGAGACCAGTGCCAAGGGCT ACCGGCGGCCTGGCTGCTCCCGACCATGCCTCGGGAGATCCGGACCGAGACCAGTGCCAAGGGCT T C TSPYL4 Ensembl:ENSG00000187189 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:116253885..116254053 26863196 MeRIP-seq:(Medium) rs1212320645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22513120 61488 RMVar_ID_61488 Human_SNP_ID_293108594 m1A Human chr6 + 116254039 116254039 116254039 ATTTTGGAAGAAGTCAGACTAGTGGGAGAGGGAGAGTTCCTTGTCCTCCGCAGCGGCCGAGCTCT ATTTTGGAAGAAGTCAGACTAGTGGGAGAGGGGGAGTTCCTTGTCCTCCGCAGCGGCCGAGCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:116253876..116254071 26863196 MeRIP-seq:(Medium) rs750925816 Functional Loss SNV dbSNP153 33..33 33 - - - 61489 RMVar_ID_61489 Human_SNP_ID_293114301 m1A Human chr6 - 116279463 116279463 116279463 TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAAGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA TGTGGTGATGGCAGCCGACCGCAGCCTGAAAATGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA T A TSPYL1 Ensembl:ENSG00000189241 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:116279251..116279562 26863196 MeRIP-seq:(Medium) rs1034648999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1324070,Human_RBP_ID_18852236 61490 RMVar_ID_61490 Human_SNP_ID_293114302 m1A Human chr6 - 116279463 116279463 116279463 TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAAGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAGGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA T C TSPYL1 Ensembl:ENSG00000189241 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:116279251..116279562 26863196 MeRIP-seq:(Medium) rs1034648999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1324070,Human_RBP_ID_18852236 61491 RMVar_ID_61491 Human_SNP_ID_293114454 m1A Human chr6 + 116279772 116279770 116279773 GTGCGTCCTGGTCGCTCGGGACTTGGTCAGAAATAATGATGCTGTGGGTTTGGAGGGGAGTGGTC GTGCGTCCTGGTCGCTCGGGACTTGGTCAGA___AATGATGCTGTGGGTTTGGAGGGGAGTGGTC AAAT A DSE Ensembl:ENSG00000111817 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:116279751..116279800 26863196 MeRIP-seq:(Medium) rs997364858 Functional Loss DEL dbSNP153 32..34 33 - - - 61492 RMVar_ID_61492 Human_SNP_ID_293114490 m1A Human chr6 + 116279849 116279849 116279849 TCCAGGCCGCTCATGTTGCTAACAGTCGGACCAACCGCAGGCGAACGCCCGTTTTCCTCAGAGGC TCCAGGCCGCTCATGTTGCTAACAGTCGGACCTACCGCAGGCGAACGCCCGTTTTCCTCAGAGGC A T DSE Ensembl:ENSG00000111817 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr6:116279751..116279900;chr6:116279356..116279853 26863410,32194978 MeRIP-seq:(Medium) rs1288485769 Functional Loss SNV dbSNP153 33..33 33 - - - 61493 RMVar_ID_61493 Human_SNP_ID_293150094 m1A Human chr6 - 116435827 116435827 116435827 CCATTGGGAGCAAAAGTAAATGAGTTTTGATCAGGATGTTCATGCCCTGCATTAAAATTTCTCCA CCATTGGGAGCAAAAGTAAATGAGTTTTGATCCGGATGTTCATGCCCTGCATTAAAATTTCTCCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:116435780..116435881 32194978 MeRIP-seq:(Medium) rs1168061644 Functional Loss SNV dbSNP153 33..33 33 - - - 61494 RMVar_ID_61494 Human_SNP_ID_293150151 m1A Human chr6 + 116436077 116436077 116436077 TTGCAGCAGAGGAGAAAAATGGGGTGGTTTTCATCCGAGGAGAAGGTGTGGGAGCTTATAACCCC TTGCAGCAGAGGAGAAAAATGGGGTGGTTTTCTTCCGAGGAGAAGGTGTGGGAGCTTATAACCCC A T Z84488.2,DSE Ensembl:ENSG00000285446,Ensembl:ENSG00000111817 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:116436030..116436180 32194978 MeRIP-seq:(Medium) rs1213902929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100788,RMVar_hsa_circ_241092,RMVar_hsa_circ_241094 61495 RMVar_ID_61495 Human_SNP_ID_293182664 m1A Human chr6 + 116571561 116571561 116571561 TGCTGCGCGCCGCCTAGGTGTCTGGGCGATCTATGGGCAAGAGCAAGGGCCACGATGACAGATTA TGCTGCGCGCCGCCTAGGTGTCTGGGCGATCTGTGGGCAAGAGCAAGGGCCACGATGACAGATTA A G RWDD1 Ensembl:ENSG00000111832 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:116571511..116571613 26863196 MeRIP-seq:(Medium) rs775932589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169321,Human_RBP_ID_651725,Human_RBP_ID_1324078,Human_RBP_ID_1662810,Human_RBP_ID_4862040,Human_RBP_ID_5477288,Human_RBP_ID_8895953,Human_RBP_ID_9401033,Human_RBP_ID_24130525,Human_RBP_ID_26354336,Human_RBP_ID_26531918,Human_RBP_ID_27087179 Human_Splice_Rec_804841,Human_Splice_Rec_804853,Human_Splice_Rec_804867,Human_Splice_Rec_804879,Human_Splice_Rec_804885 Human_miRNA_ID_2426724 RMVar_hsa_circ_241097,RMVar_hsa_circ_111308 61496 RMVar_ID_61496 Human_SNP_ID_293182680 m1A Human chr6 + 116571588 116571588 116571588 GATCTATGGGCAAGAGCAAGGGCCACGATGACAGATTACGGCGAGGAGCAGCGCAACGAGCTGGA GATCTATGGGCAAGAGCAAGGGCCACGATGACCGATTACGGCGAGGAGCAGCGCAACGAGCTGGA A C RWDD1 Ensembl:ENSG00000111832 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:116571484..116571625 26863196 MeRIP-seq:(Medium) rs145335718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79347,Human_RBP_ID_169321,Human_RBP_ID_4904230,Human_RBP_ID_8628363,Human_RBP_ID_9336277,Human_RBP_ID_9401033,Human_RBP_ID_15617482,Human_RBP_ID_18852271,Human_RBP_ID_24130526,Human_RBP_ID_26354336,Human_RBP_ID_26828748,Human_RBP_ID_27087179 Human_Splice_Rec_804841,Human_Splice_Rec_804853,Human_Splice_Rec_804867,Human_Splice_Rec_804879,Human_Splice_Rec_804885 RMVar_hsa_circ_241097,RMVar_hsa_circ_111308 61497 RMVar_ID_61497 Human_SNP_ID_293187442 m1A Human chr6 - 116593107 116593107 116593107 TGTGGCAGTCAAGCCTCTCTGCAGATGGGGACAGTCCATTAGTCAGCTGAGTCACTCTCTGGGTC TGTGGCAGTCAAGCCTCTCTGCAGATGGGGACGGTCCATTAGTCAGCTGAGTCACTCTCTGGGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:116593057..116593207 32194978 MeRIP-seq:(Medium) rs778035529 Functional Loss SNV dbSNP153 33..33 33 - - - 61498 RMVar_ID_61498 Human_SNP_ID_293187443 m1A Human chr6 - 116593107 116593107 116593107 TGTGGCAGTCAAGCCTCTCTGCAGATGGGGACAGTCCATTAGTCAGCTGAGTCACTCTCTGGGTC TGTGGCAGTCAAGCCTCTCTGCAGATGGGGACCGTCCATTAGTCAGCTGAGTCACTCTCTGGGTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:116593057..116593207 32194978 MeRIP-seq:(Medium) rs778035529 Functional Loss SNV dbSNP153 33..33 33 - - - 61499 RMVar_ID_61499 Human_SNP_ID_293208630 m1A Human chr6 - 116681270 116681270 116681270 AGTCCCCAGCGGCGACGTGTGTGGCGGGTAACAGAAGGGCCGCCACTCCGCCCCTGGCGTGAAGC AGTCCCCAGCGGCGACGTGTGTGGCGGGTAACTGAAGGGCCGCCACTCCGCCCCTGGCGTGAAGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:116681220..116681386 26863196 MeRIP-seq:(Medium) rs893521027 Functional Loss SNV dbSNP153 33..33 33 - - - 61500 RMVar_ID_61500 Human_SNP_ID_293208631 m1A Human chr6 + 116681274 116681274 116681274 CACGCCAGGGGCGGAGTGGCGGCCCTTCTGTTACCCGCCACACACGTCGCCGCTGGGGACTGGGA CACGCCAGGGGCGGAGTGGCGGCCCTTCTGTTCCCCGCCACACACGTCGCCGCTGGGGACTGGGA A C KPNA5 Ensembl:ENSG00000196911 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:116681228..116681371;chr6:116681227..116681385 26863196 MeRIP-seq:(Medium) rs960745047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_651790 Human_Splice_Rec_804967,Human_Splice_Rec_804975,Human_Splice_Rec_805001 61501 RMVar_ID_61501 Human_SNP_ID_293208660 m1A Human chr6 - 116681333 116681333 116681333 ACCTAGCCCGTGTTCACTCCAACTTACCCATTAATGTGGCACTCTCCGATGCCCTGATTTCCCAG ACCTAGCCCGTGTTCACTCCAACTTACCCATTGATGTGGCACTCTCCGATGCCCTGATTTCCCAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:116681210..116681338 26863196 MeRIP-seq:(Medium) rs1360751211 Functional Loss SNV dbSNP153 33..33 33 - - - 61502 RMVar_ID_61502 Human_SNP_ID_293336884 m1A Human chr6 + 117208501 117208501 117208501 CTGGTAACCATCCTTCTACTCACCCCCTAACTACCCTTTCCAGCTCCTGGTAACCATCCTTCTAC CTGGTAACCATCCTTCTACTCACCCCCTAACTTCCCTTTCCAGCTCCTGGTAACCATCCTTCTAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:117208452..117208544 26863196 MeRIP-seq:(Medium) rs1178103908 Functional Loss SNV dbSNP153 33..33 33 - - - 61503 RMVar_ID_61503 Human_SNP_ID_293336888 m1A Human chr6 - 117208513 117208513 117208513 TGGTTATAAAGAGTAGAAGGATGGTTACCAGGAGCTGGAAAGGGTAGTTAGGGGGTGAGTAGAAG TGGTTATAAAGAGTAGAAGGATGGTTACCAGGGGCTGGAAAGGGTAGTTAGGGGGTGAGTAGAAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:117208462..117208570 26863196 MeRIP-seq:(Medium) rs1445251823 Functional Loss SNV dbSNP153 33..33 33 - - - 61504 RMVar_ID_61504 Human_SNP_ID_293409071 m1A Human chr6 - 117503731 117503729 117503732 GTAAAGAAAAAGAAGGGGGGAATAAAAGAAGAAGGGGTCATTAATTCTTACTGAGGATTGAGAGT GTAAAGAAAAAGAAGGGGGGAATAAAAGAAG___GGGTCATTAATTCTTACTGAGGATTGAGAGT CCTT C AL132671.2 Ensembl:ENSG00000282218 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:117503729..117503797 26863196 MeRIP-seq:(Medium) rs1474634827 Functional Loss DEL dbSNP153 32..34 33 - - - 61505 RMVar_ID_61505 Human_SNP_ID_293449107 m1A Human chr6 - 117675555 117675543 117675556 CGGGCCATCGCTCCGCGTCCCCCCGCCCCCCGAGCCCGAACCCCTTTCCACTGCCAACACCTCAC CGGGCCATCGCTCCGCGTCCCCCCGCCCCCC_____________TTTCCACTGCCAACACCTCAC AGGGGTTCGGGCTC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:117675501..117675651;chr6:117675501..117675661;chr6:117675501..117675663 26863196 MeRIP-seq:(Medium) rs1282663723 Functional Loss DEL dbSNP153 32..44 33 - - - 61506 RMVar_ID_61506 Human_SNP_ID_293449134 m1A Human chr6 + 117675639 117675602 117675639 TAAAAAGCCGTCGCGCTGCGGGAGTGGGCGGGAGGGAGAGGGGGTGTCTGAGGGCCACAAGAGTA _________________________________GGGAGAGGGGGTGTCTGAGGGCCACAAGAGTA GCGGATAAAAAGCCGTCGCGCTGCGGGAGTGGGCGGGA G NUS1 Ensembl:ENSG00000153989 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:117675548..117675642 26863410 MeRIP-seq:(Medium) rs1356548623 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_18957639 61507 RMVar_ID_61507 Human_SNP_ID_293449164 m1A Human chr6 + 117675639 117675639 117675639 TAAAAAGCCGTCGCGCTGCGGGAGTGGGCGGGAGGGAGAGGGGGTGTCTGAGGGCCACAAGAGTA TAAAAAGCCGTCGCGCTGCGGGAGTGGGCGGGGGGGAGAGGGGGTGTCTGAGGGCCACAAGAGTA A G NUS1 Ensembl:ENSG00000153989 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:117675548..117675642 26863410 MeRIP-seq:(Medium) rs766506214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18957639 61508 RMVar_ID_61508 Human_SNP_ID_293449257 m1A Human chr6 - 117675803 117675803 117675803 CGTGAAGCCGAGCGGCGCTAGGACCGCGGCAGAGGCGGCGCGGCAGCAGCGCCGCCAGATCCAGT CGTGAAGCCGAGCGGCGCTAGGACCGCGGCAGCGGCGGCGCGGCAGCAGCGCCGCCAGATCCAGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:117675750..117675850;chr6:117675745..117675850 26863196 MeRIP-seq:(Medium) rs1238893479 Functional Loss SNV dbSNP153 33..33 33 - - - 61509 RMVar_ID_61509 Human_SNP_ID_293449274 m1A Human chr6 - 117675837 117675837 117675837 GGCGGTTCCTGCCGACTGCCGGGGGCTTGCGGAGCGTGAAGCCGAGCGGCGCTAGGACCGCGGCA GGCGGTTCCTGCCGACTGCCGGGGGCTTGCGGGGCGTGAAGCCGAGCGGCGCTAGGACCGCGGCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:117675751..117675850 26863410 MeRIP-seq:(Medium) rs1373437089 Functional Loss SNV dbSNP153 33..33 33 - - - 61510 RMVar_ID_61510 Human_SNP_ID_293452537 m1A Human chr6 - 117689123 117689123 117689123 CTCAAAATTCTATCTTTATCCCAACTTGTCTCAATGTTCTCTTCCTGATTCAACACGTAACCTGG CTCAAAATTCTATCTTTATCCCAACTTGTCTCGATGTTCTCTTCCTGATTCAACACGTAACCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:117689015..117689215 26863196 MeRIP-seq:(Medium) rs1309145763 Functional Loss SNV dbSNP153 33..33 33 - - - 61511 RMVar_ID_61511 Human_SNP_ID_293528753 m1A Human chr6 + 117998953 117998953 117998953 AAATCAGCTCTTCCGGTTCTAGGCACTTCGGGAGCCGCGGCTTATGGTGCAGACATGGCCAAGTC AAATCAGCTCTTCCGGTTCTAGGCACTTCGGGCGCCGCGGCTTATGGTGCAGACATGGCCAAGTC A C SLC35F1 Ensembl:ENSG00000196376 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1313946295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81903,Human_RBP_ID_652015,Human_RBP_ID_4906801,Human_RBP_ID_8628696,Human_RBP_ID_9186344,Human_RBP_ID_15621878,Human_RBP_ID_17304467,Human_RBP_ID_17421854,Human_RBP_ID_18062002,Human_RBP_ID_22304986,Human_RBP_ID_24131243,Human_RBP_ID_26540564,Human_RBP_ID_27340242,Human_RBP_ID_27567875 61512 RMVar_ID_61512 Human_SNP_ID_293684474 m1A Human chr6 - 118651326 118651326 118651326 CGCTCCGCGCAAGTTTCCGCCGCCGAAGAAGCAGGAGGACGGACGTGAGGAGTCGGGCGTCCCTG CGCTCCGCGCAAGTTTCCGCCGCCGAAGAAGCCGGAGGACGGACGTGAGGAGTCGGGCGTCCCTG T G CEP85L Ensembl:ENSG00000111860 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:118651279..118651450 26863196 MeRIP-seq:(Medium) rs1001291615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22105362 RMVar_hsa_circ_107859,RMVar_hsa_circ_241159,RMVar_hsa_circ_92256,RMVar_hsa_circ_124480,RMVar_hsa_circ_241169,RMVar_hsa_circ_241178,RMVar_hsa_circ_56725,RMVar_hsa_circ_241175,RMVar_hsa_circ_70180,RMVar_hsa_circ_338743,RMVar_hsa_circ_350009 61513 RMVar_ID_61513 Human_SNP_ID_293684521 m1A Human chr6 + 118651452 118651450 118651452 CGGGCGGGGAGCGCAGGGGCCAGATTCGCCGCACTGCCGGCGCCTGCCATGGCCAAGCCGGCTGG CGGGCGGGGAGCGCAGGGGCCAGATTCGCCG__CTGCCGGCGCCTGCCATGGCCAAGCCGGCTGG GCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:118651358..118651559 26863410 MeRIP-seq:(Medium) rs1327087291 Functional Loss DEL dbSNP153 32..33 33 - - - 61514 RMVar_ID_61514 Human_SNP_ID_293684554 m1A Human chr6 - 118651528 118651528 118651528 CCTTTGAGCCTGGGCTCAGCCGGGGATCTAGCAGCCGTCACCGCCGAGTCGCCGCTTCCCCGGCG CCTTTGAGCCTGGGCTCAGCCGGGGATCTAGCGGCCGTCACCGCCGAGTCGCCGCTTCCCCGGCG T C CEP85L Ensembl:ENSG00000111860 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:118651483..118651557 26863196 MeRIP-seq:(Medium) rs1420470100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107859,RMVar_hsa_circ_241159,RMVar_hsa_circ_92256,RMVar_hsa_circ_124480,RMVar_hsa_circ_241169,RMVar_hsa_circ_241178,RMVar_hsa_circ_56725,RMVar_hsa_circ_241175,RMVar_hsa_circ_70180,RMVar_hsa_circ_338743,RMVar_hsa_circ_350009 61515 RMVar_ID_61515 Human_SNP_ID_293752499 m1A Human chr6 - 118935070 118935070 118935070 GAGAGCGCAGGCCCGGCAGAGCCGCAGGCGCTAGGCCGCCCGACACAGCCCGCGCGTCCCCGCGG GAGAGCGCAGGCCCGGCAGAGCCGCAGGCGCTGGGCCGCCCGACACAGCCCGCGCGTCCCCGCGG T C MCM9 Ensembl:ENSG00000111877 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:118934974..118935100 26863410 MeRIP-seq:(Medium) rs1245411786 Functional Loss SNV dbSNP153 33..33 33 - - - 61516 RMVar_ID_61516 Human_SNP_ID_430713563 m1A Human chr10 - 45003854 45003854 45003854 CCACATTCACTGCACTGGTAGGGTTTCTCCCCAGTGTGGGTTCTCTGATGTTGAATAAGGTGGGA CCACATTCACTGCACTGGTAGGGTTTCTCCCCGGTGTGGGTTCTCTGATGTTGAATAAGGTGGGA T C CEP164P1 Ensembl:ENSG00000226937 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:45003805..45004053 32194978 MeRIP-seq:(Medium) rs750115594 Functional Loss SNV dbSNP153 33..33 33 - - - 61517 RMVar_ID_61517 Human_SNP_ID_430894835 m1A Human chr10 - 45727010 45727010 45727010 GGCGGGGGGCGCTGCCGCCCAAGGCCCGAGGCAGCGGCGCGGGATCGGCCAAAGCACCGGCCGCC GGCGGGGGGCGCTGCCGCCCAAGGCCCGAGGCGGCGGCGCGGGATCGGCCAAAGCACCGGCCGCC T C FAM21FP Ensembl:ENSG00000237840 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:45726960..45727051 26863196 MeRIP-seq:(Medium) rs889243594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5546744 61518 RMVar_ID_61518 Human_SNP_ID_430894995 m1A Human chr10 + 45727303 45727303 45727303 TCGGCCTGTGCTGGCAGCCTCGGAGCCCACCGAGCCGGGCGGCTGGGATGGTGAGGGCGGCGGGC TCGGCCTGTGCTGGCAGCCTCGGAGCCCACCGCGCCGGGCGGCTGGGATGGTGAGGGCGGCGGGC A C WASHC2C Ensembl:ENSG00000172661 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:45727261..45727484;chr10:45727255..45727455 26863196 MeRIP-seq:(Medium) rs1044010304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225957,Human_RBP_ID_4136263,Human_RBP_ID_22886866 Human_Splice_Rec_1128821,Human_Splice_Rec_1128877,Human_Splice_Rec_1128935,Human_Splice_Rec_1128991,Human_Splice_Rec_1129045,Human_Splice_Rec_1129103,Human_Splice_Rec_1129163 61519 RMVar_ID_61519 Human_SNP_ID_430900826 m1A Human chr10 - 45750840 45750836 45750840 TCCCCTACTCCCCATCAACGTGGCTGGGGCTCACTTGTCGGCTCCTCGTCCACTCGACCCATGGC TCCCCTACTCCCCATCAACGTGGCTGGGGCTC____GTCGGCTCCTCGTCCACTCGACCCATGGC CAAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:45750790..45750871 26863196 MeRIP-seq:(Medium) rs1180739706 Functional Loss DEL dbSNP153 33..36 33 - - - 61520 RMVar_ID_61520 Human_SNP_ID_430949881 m1A Human chr10 - 45962986 45962986 45962986 TAAATACATTTGTCTTGACCTTAGAAAAGAACAATGGGAAACCAAACATCAAAGAACAGAAAGGA TAAATACATTTGTCTTGACCTTAGAAAAGAACTATGGGAAACCAAACATCAAAGAACAGAAAGGA T A PARGP1 Ensembl:ENSG00000239883 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:45962973..45963057 26863196 MeRIP-seq:(Medium) rs1274749925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26317141 Human_Splice_Rec_1129298 RMVar_hsa_circ_336805,RMVar_hsa_circ_280364,RMVar_hsa_circ_270114,RMVar_hsa_circ_21520,RMVar_hsa_circ_290869,RMVar_hsa_circ_57731,RMVar_hsa_circ_12229,RMVar_hsa_circ_352313,RMVar_hsa_circ_270082,RMVar_hsa_circ_270014,RMVar_hsa_circ_355104,RMVar_hsa_circ_70985 61521 RMVar_ID_61521 Human_SNP_ID_430952007 m1A Human chr10 - 45972344 45972344 45972344 GCATTGAGGCAGGTGGGGTGCCAGTGGAAGAGAGAAAGCAGGCGAGTGTTTACGGCCTGACTTGG GCATTGAGGCAGGTGGGGTGCCAGTGGAAGAGGGAAAGCAGGCGAGTGTTTACGGCCTGACTTGG T C HSALNG0077912 RNACentral:URS0000EAFE47 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:45972278..45972379;chr10:45972202..45972369;chr10:45972225..45972374;chr10:45972196..45972373 31548705,26863196 m1A-IP-seq:(High) rs74856023 Functional Loss SNV dbSNP153 33..33 33 - - - 61522 RMVar_ID_61522 Human_SNP_ID_430952148 m1A Human chr10 + 45972658 45972658 45972658 TGGAAGGAGGCGGGGGAAGCGGCAACAAAACCACAGGGGGATTGGCCGGCTTTTTCGGAGCCGGC TGGAAGGAGGCGGGGGAAGCGGCAACAAAACCTCAGGGGGATTGGCCGGCTTTTTCGGAGCCGGC A T TIMM23 Ensembl:ENSG00000265354 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:45972497..45972679 26863196 MeRIP-seq:(Medium) rs782262599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136264,Human_RBP_ID_9361235,Human_RBP_ID_26316250 Human_Splice_Rec_1129315 61523 RMVar_ID_61523 Human_SNP_ID_430954721 m1A Human chr10 + 45982603 45982603 45982603 AGATTTGAGCTGGCCTTCTTTACGATTGGAGGATGTTGCATGACAGGTGAGTGTTACATACTTTT AGATTTGAGCTGGCCTTCTTTACGATTGGAGGCTGTTGCATGACAGGTGAGTGTTACATACTTTT A C TIMM23 Ensembl:ENSG00000265354 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61849495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17787005 Human_Splice_Rec_1129318,Human_Splice_Rec_1129319 RMVar_hsa_circ_274417,RMVar_hsa_circ_364622,RMVar_hsa_circ_2354,RMVar_hsa_circ_271858,RMVar_hsa_circ_338423 61524 RMVar_ID_61524 Human_SNP_ID_430954722 m1A Human chr10 + 45982603 45982603 45982603 AGATTTGAGCTGGCCTTCTTTACGATTGGAGGATGTTGCATGACAGGTGAGTGTTACATACTTTT AGATTTGAGCTGGCCTTCTTTACGATTGGAGGGTGTTGCATGACAGGTGAGTGTTACATACTTTT A G TIMM23 Ensembl:ENSG00000265354 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61849495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17787005 Human_Splice_Rec_1129318,Human_Splice_Rec_1129319 RMVar_hsa_circ_274417,RMVar_hsa_circ_364622,RMVar_hsa_circ_2354,RMVar_hsa_circ_271858,RMVar_hsa_circ_338423 61525 RMVar_ID_61525 Human_SNP_ID_430960503 m1A Human chr10 + 46005182 46005182 46005182 CATACTCATTAACATAGTGATTAATGTAAATTATATTTTGACTTGTAAAATACAGTGTGTTTGGC CATACTCATTAACATAGTGATTAATGTAAATTGTATTTTGACTTGTAAAATACAGTGTGTTTGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:46005137..46005287 32194978 MeRIP-seq:(Medium) rs1170625365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1447012,Human_RBP_ID_1767097,Human_RBP_ID_18241696,Human_RBP_ID_27607991 RMVar_hsa_circ_96127,RMVar_hsa_circ_143390,RMVar_hsa_circ_143394,RMVar_hsa_circ_143396,RMVar_hsa_circ_143384,RMVar_hsa_circ_143389,RMVar_hsa_circ_119392,RMVar_hsa_circ_84765,RMVar_hsa_circ_87154,RMVar_hsa_circ_82047 61526 RMVar_ID_61526 Human_SNP_ID_430962065 m1A Human chr10 - 46010690 46010690 46010690 TAGAGGAGGTGTGCAGAGCCAATGAGCCCTGCACAAGCTTTGCAGAGTGTGTGTGTGATGAGAAT TAGAGGAGGTGTGCAGAGCCAATGAGCCCTGCGCAAGCTTTGCAGAGTGTGTGTGTGATGAGAAT T C NCOA4 Ensembl:ENSG00000266412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:46010648..46010792 26863196 MeRIP-seq:(Medium) rs141175678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9254047,Human_RBP_ID_9273805,Human_RBP_ID_17647972,Human_RBP_ID_22431407,Human_RBP_ID_23458451 RMVar_hsa_circ_23807,RMVar_hsa_circ_346999,RMVar_hsa_circ_63681,RMVar_hsa_circ_301910,RMVar_hsa_circ_288602 61527 RMVar_ID_61527 Human_SNP_ID_430967105 m1A Human chr10 + 46030575 46030575 46030575 CCAGGCGATCCGAGGAGACCTTGGGTGGACTGAGACACGGCCCCACACTAACCTACGGCCCAAAG CCAGGCGATCCGAGGAGACCTTGGGTGGACTGCGACACGGCCCCACACTAACCTACGGCCCAAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:46030472..46030600;chr10:46030475..46030625;chr10:46030480..46030650 26863196 MeRIP-seq:(Medium) rs1554926367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1980690,Human_miRNA_ID_1982414,Human_miRNA_ID_3079696 61528 RMVar_ID_61528 Human_SNP_ID_430986743 m1A Human chr10 - 46106977 46106973 46106977 AGGCAGGGGACAGGAACAGGAATGGGACTCAGAGAGGACCTGGGAGAATGCGGGAGGAAGCTGGC AGGCAGGGGACAGGAACAGGAATGGGACTCAG____GACCTGGGAGAATGCGGGAGGAAGCTGGC CCTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:46106959..46107072 26863196 MeRIP-seq:(Medium) rs1244205602 Functional Loss DEL dbSNP153 33..36 33 - - - 61529 RMVar_ID_61529 Human_SNP_ID_430986747 m1A Human chr10 - 46106977 46106977 46106977 AGGCAGGGGACAGGAACAGGAATGGGACTCAGAGAGGACCTGGGAGAATGCGGGAGGAAGCTGGC AGGCAGGGGACAGGAACAGGAATGGGACTCAGGGAGGACCTGGGAGAATGCGGGAGGAAGCTGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:46106959..46107072 26863196 MeRIP-seq:(Medium) rs1554937264 Functional Loss SNV dbSNP153 33..33 33 - - - 61530 RMVar_ID_61530 Human_SNP_ID_431029134 m1A Human chr10 + 46284395 46284395 46284395 AGACAGGGACAGCAATGGGACTCGGAAAGGACATGGGAGAGAGCTGGAGGAAGCTGACAGAGGGA AGACAGGGACAGCAATGGGACTCGGAAAGGACGTGGGAGAGAGCTGGAGGAAGCTGACAGAGGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:46284292..46284421 26863196 MeRIP-seq:(Medium) rs970001552 Functional Loss SNV dbSNP153 33..33 33 - - - 61531 RMVar_ID_61531 Human_SNP_ID_431087880 m1A Human chr10 + 46526341 46526337 46526341 CTCACACACAAATTCACAACCACATACGTCACACACACAACCACACACACCACAACCACACACAT CTCACACACAAATTCACAACCACATACGT____CACACAACCACACACACCACAACCACACACAT TCACA T AC244230.2 Ensembl:ENSG00000285402 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:46526300..46526385 26863196 MeRIP-seq:(Medium) rs1175872394 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_2218352 61532 RMVar_ID_61532 Human_SNP_ID_431087881 m1A Human chr10 + 46526341 46526337 46526341 CTCACACACAAATTCACAACCACATACGTCACACACACAACCACACACACCACAACCACACACAT CTCACACACAAATTCACAACCACATACGTCA__CACACAACCACACACACCACAACCACACACAT TCACA TCA AC244230.2 Ensembl:ENSG00000285402 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:46526300..46526385 26863196 MeRIP-seq:(Medium) rs1175872394 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2218352 61533 RMVar_ID_61533 Human_SNP_ID_431087884 m1A Human chr10 + 46526341 46526341 46526341 CTCACACACAAATTCACAACCACATACGTCACACACACAACCACACACACCACAACCACACACAT CTCACACACAAATTCACAACCACATACGTCACTCACACAACCACACACACCACAACCACACACAT A T AC244230.2 Ensembl:ENSG00000285402 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:46526300..46526385 26863196 MeRIP-seq:(Medium) rs1171661019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2218352 61534 RMVar_ID_61534 Human_SNP_ID_431090946 m1A Human chr10 - 46535364 46535361 46535364 AGAGAGGAGAGAGAGAGAGAGAACAGAGAGACAGAGGAGAGAAAGAGACAGAGGAGAGAGAGAGG AGAGAGGAGAGAGAGAGAGAGAACAGAGAGAC___GGAGAGAAAGAGACAGAGGAGAGAGAGAGG CTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:46535251..46535479 26863196 MeRIP-seq:(Medium) rs1442527604 Functional Loss DEL dbSNP153 33..35 33 - - - 61535 RMVar_ID_61535 Human_SNP_ID_431098824 m1A Human chr10 + 46556552 46556552 46556552 CAGGCGGGGGAAGCGCTGCTCCTGCGGCCGCCACAGGTGCCAGGTGCCGCGGCCCAAGATGGAGC CAGGCGGGGGAAGCGCTGCTCCTGCGGCCGCCCCAGGTGCCAGGTGCCGCGGCCCAAGATGGAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:46556448..46556568 26863196 MeRIP-seq:(Medium) rs1393406630 Functional Loss SNV dbSNP153 33..33 33 - - - 61536 RMVar_ID_61536 Human_SNP_ID_431111988 m1A Human chr10 + 46597484 46597484 46597484 TGTGGACAAGAGAGATGGGAGGATCCGGGAGGATGTGCTGTTTCTCAGGGTCCCACAGCTAGAAG TGTGGACAAGAGAGATGGGAGGATCCGGGAGGGTGTGCTGTTTCTCAGGGTCCCACAGCTAGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:46597476..46597541 26863196 MeRIP-seq:(Medium) rs1442989093 Functional Loss SNV dbSNP153 33..33 33 - - - 61537 RMVar_ID_61537 Human_SNP_ID_431116864 m1A Human chr10 - 46621715 46621715 46621715 TGAAGAGTATTTTTTCTTCTCTTCCCAACATCATATATACTGGCTGTGCAAAATGTGGATTGGAA TGAAGAGTATTTTTTCTTCTCTTCCCAACATCGTATATACTGGCTGTGCAAAATGTGGATTGGAA T C SHLD2P1 Ensembl:ENSG00000165874 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1555051039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15091 61538 RMVar_ID_61538 Human_SNP_ID_431118778 m1A Human chr10 - 46635113 46635113 46635113 GGGAAAGTACAAATACCTATTATGTTGGTTGGAAATAAGAAAGACCTGCATATGGAAAGGGTGAT GGGAAAGTACAAATACCTATTATGTTGGTTGGGAATAAGAAAGACCTGCATATGGAAAGGGTGAT T C RHEBP1,SHLD2P1 Ensembl:ENSG00000229927,Ensembl:ENSG00000165874 Pseudogene,Pseudogene exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1162299926 Functional Loss SNV dbSNP153 33..33 33 - - - 61539 RMVar_ID_61539 Human_SNP_ID_431147233 m1A Human chr10 - 46786775 46786775 46786775 AAGGCAGAAAAAAAGGGACCGCCGCCTGGACGACTTGCAGGGGACAGCTGGAAGAAAGACTCGTC AAGGCAGAAAAAAAGGGACCGCCGCCTGGACGGCTTGCAGGGGACAGCTGGAAGAAAGACTCGTC T C lnc-GPRIN2-4 RNACentral:URS00009B9C00 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:46786724..46786855 26863196 MeRIP-seq:(Medium) rs1232312477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1129897 61540 RMVar_ID_61540 Human_SNP_ID_431382769 m1A Human chr10 - 47930099 47930098 47930099 CAAGAGTAGGAAGTAGAAAGGCCTGAGGCGGGAGAGGTCTTAGCCTGTTCAAAAGATAGCAGAGA CAAGAGTAGGAAGTAGAAAGGCCTGAGGCGGG_GAGGTCTTAGCCTGTTCAAAAGATAGCAGAGA CT C AC245041.2 Ensembl:ENSG00000276850 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:47930061..47930131;chr10:47930053..47930137 26863196 MeRIP-seq:(Medium) rs1419884383 Functional Loss DEL dbSNP153 33..33 33 - - - 61541 RMVar_ID_61541 Human_SNP_ID_431591068 m1A Human chr10 + 48809519 48809519 48809519 TCATAACCACTACCACCATCAACATCATCACCATCACCACCAGCATCACCATCACCATAATCACC TCATAACCACTACCACCATCAACATCATCACCGTCACCACCAGCATCACCATCACCATAATCACC A G WDFY4 Ensembl:ENSG00000128815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:48809469..48809571 26863196 MeRIP-seq:(Medium) rs1203350836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83481,RMVar_hsa_circ_82154,RMVar_hsa_circ_143353,RMVar_hsa_circ_82440,RMVar_hsa_circ_92366,RMVar_hsa_circ_143356,RMVar_hsa_circ_143357,RMVar_hsa_circ_104375,RMVar_hsa_circ_86168,RMVar_hsa_circ_143358,RMVar_hsa_circ_377156,RMVar_hsa_circ_143359,RMVar_hsa_circ_143360 61542 RMVar_ID_61542 Human_SNP_ID_431765810 m1A Human chr10 + 49481809 49481809 49481809 GTCAGCCTCCAAACCTTGTTTGTTCTGCCTAAAAATGCCACCTGCGTCTCCTGCCCCACCATCTT GTCAGCCTCCAAACCTTGTTTGTTCTGCCTAACAATGCCACCTGCGTCTCCTGCCCCACCATCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:49481758..49481849 26863196 MeRIP-seq:(Medium) rs1237318395 Functional Loss SNV dbSNP153 33..33 33 - - - 61543 RMVar_ID_61543 Human_SNP_ID_431765830 m1A Human chr10 - 49481873 49481873 49481873 CTGCAGGAACCACTGGGGTGAGGGCCATGAGGACCTGGACCTGATCTTGGGTGGTGGTCTGAGAA CTGCAGGAACCACTGGGGTGAGGGCCATGAGGGCCTGGACCTGATCTTGGGTGGTGGTCTGAGAA T C ERCC6 Ensembl:ENSG00000225830 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:49481666..49481914 26863196 MeRIP-seq:(Medium) rs542157937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22158,RMVar_hsa_circ_351565,RMVar_hsa_circ_354290,RMVar_hsa_circ_333714,RMVar_hsa_circ_70959,RMVar_hsa_circ_143365,RMVar_hsa_circ_23846,RMVar_hsa_circ_21178,RMVar_hsa_circ_56918,RMVar_hsa_circ_353964,RMVar_hsa_circ_267720,RMVar_hsa_circ_362854,RMVar_hsa_circ_14447,RMVar_hsa_circ_67938,RMVar_hsa_circ_51962,RMVar_hsa_circ_62428,RMVar_hsa_circ_99506,RMVar_hsa_circ_143366,RMVar_hsa_circ_57530 61544 RMVar_ID_61544 Human_SNP_ID_431774856 m1A Human chr10 + 49519845 49519845 49519845 ATGAAGAATGTCACCAAGCTCCCCTCAGAGTCAGCGGGAGCTCAGCCAAAGCACAAGTGCAGTGC ATGAAGAATGTCACCAAGCTCCCCTCAGAGTCTGCGGGAGCTCAGCCAAAGCACAAGTGCAGTGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:49519843..49520006 26863196 MeRIP-seq:(Medium) rs1249069258 Functional Loss SNV dbSNP153 33..33 33 - - - 61545 RMVar_ID_61545 Human_SNP_ID_431775826 m1A Human chr10 - 49524095 49524092 49524095 GAAGCTGCTTCTGTAGGAGAAGGAGGAGGAGGAGGTCGGAAAGTGGGAAGATACCGAGATGATGG GAAGCTGCTTCTGTAGGAGAAGGAGGAGGAGG___TCGGAAAGTGGGAAGATACCGAGATGATGG ACCT A ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:49524044..49524448 26863196 MeRIP-seq:(Medium) rs745524303 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5974050,Human_RBP_ID_26316260 Human_Splice_Rec_1131769,Human_Splice_Rec_1131891,Human_Splice_Rec_1131901 RMVar_hsa_circ_70959,RMVar_hsa_circ_267720,RMVar_hsa_circ_67938,RMVar_hsa_circ_62428,RMVar_hsa_circ_362021,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_59124,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_367416,RMVar_hsa_circ_315857 61546 RMVar_ID_61546 Human_SNP_ID_431775906 m1A Human chr10 - 49524282 49524282 49524282 TGAGTATTTCCCCACAGAGGAGGAGGAAGAGGAGGAAGATGACGAGGTGGAGGGGGCAGAGGCGG TGAGTATTTCCCCACAGAGGAGGAGGAAGAGGGGGAAGATGACGAGGTGGAGGGGGCAGAGGCGG T C ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:49523999..49524425 26863196 MeRIP-seq:(Medium) rs747814000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861180,Human_RBP_ID_3938239,Human_RBP_ID_9343547,Human_RBP_ID_26316261 RMVar_hsa_circ_70959,RMVar_hsa_circ_267720,RMVar_hsa_circ_67938,RMVar_hsa_circ_62428,RMVar_hsa_circ_362021,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_59124,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_367416,RMVar_hsa_circ_315857 61547 RMVar_ID_61547 Human_SNP_ID_431775921 m1A Human chr10 - 49524318 49524316 49524318 GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAGAGTCTGAGTATTTCCCCACAGAGGAGGAGGAAG GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAG__TCTGAGTATTTCCCCACAGAGGAGGAGGAAG ACT A ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:49524267..49524356 26863196 MeRIP-seq:(Medium) rs759698849 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_378160,Human_RBP_ID_861180,Human_RBP_ID_9343547,Human_RBP_ID_26316261 RMVar_hsa_circ_70959,RMVar_hsa_circ_267720,RMVar_hsa_circ_67938,RMVar_hsa_circ_62428,RMVar_hsa_circ_362021,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_59124,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_367416,RMVar_hsa_circ_315857 61548 RMVar_ID_61548 Human_SNP_ID_431775923 m1A Human chr10 - 49524318 49524318 49524318 GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAGAGTCTGAGTATTTCCCCACAGAGGAGGAGGAAG GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAGTGTCTGAGTATTTCCCCACAGAGGAGGAGGAAG T A ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:49524267..49524356 26863196 MeRIP-seq:(Medium) rs774833290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378160,Human_RBP_ID_861180,Human_RBP_ID_9343547,Human_RBP_ID_26316261 RMVar_hsa_circ_70959,RMVar_hsa_circ_267720,RMVar_hsa_circ_67938,RMVar_hsa_circ_62428,RMVar_hsa_circ_362021,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_59124,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_367416,RMVar_hsa_circ_315857 61549 RMVar_ID_61549 Human_SNP_ID_431775924 m1A Human chr10 - 49524318 49524318 49524318 GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAGAGTCTGAGTATTTCCCCACAGAGGAGGAGGAAG GCCAGAGGCAGAGGGAGACTCTGAGGGTGAAGGGTCTGAGTATTTCCCCACAGAGGAGGAGGAAG T C ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:49524267..49524356 26863196 MeRIP-seq:(Medium) rs774833290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378160,Human_RBP_ID_861180,Human_RBP_ID_9343547,Human_RBP_ID_26316261 RMVar_hsa_circ_70959,RMVar_hsa_circ_267720,RMVar_hsa_circ_67938,RMVar_hsa_circ_62428,RMVar_hsa_circ_362021,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_59124,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_367416,RMVar_hsa_circ_315857 61550 RMVar_ID_61550 Human_SNP_ID_431778247 m1A Human chr10 - 49532927 49532927 49532927 AAATGAGGGAATCCCCCACTCAAGTCAAACTCAGGAGCAAGACTGTTTACAGAGTCAACCTGTCA AAATGAGGGAATCCCCCACTCAAGTCAAACTCCGGAGCAAGACTGTTTACAGAGTCAACCTGTCA T G ERCC6 Ensembl:ENSG00000225830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:49532876..49532987 26863196 MeRIP-seq:(Medium) rs748261677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2219816,Human_RBP_ID_8334863,Human_RBP_ID_26316265 Human_Splice_Rec_1131762,Human_Splice_Rec_1131884,Human_Splice_Rec_1131894,Human_Splice_Rec_1131908 Human_miRNA_ID_2026244,Human_miRNA_ID_2215887,Human_miRNA_ID_2335138,Human_miRNA_ID_2337372,Human_miRNA_ID_2339605,Human_miRNA_ID_2341840,Human_miRNA_ID_2344076,Human_miRNA_ID_2611251 RMVar_hsa_circ_267720,RMVar_hsa_circ_275056,RMVar_hsa_circ_368504,RMVar_hsa_circ_83295,RMVar_hsa_circ_143371,RMVar_hsa_circ_351313,RMVar_hsa_circ_143372 61551 RMVar_ID_61551 Human_SNP_ID_431877011 m1A Human chr10 - 49942084 49942084 49942084 GCGGGTAACCCCGCGTTGCCAGCGCCTACTTCACACGCTGACATTCCGGGCGCCGGTTCCCGTTA GCGGGTAACCCCGCGTTGCCAGCGCCTACTTCGCACGCTGACATTCCGGGCGCCGGTTCCCGTTA T C PARG Ensembl:ENSG00000227345 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:49942067..49942185 26863196 MeRIP-seq:(Medium) rs1464384032 Functional Loss SNV dbSNP153 33..33 33 - - - 61552 RMVar_ID_61552 Human_SNP_ID_431877034 m1A Human chr10 + 49942131 49942131 49942131 CAACGCGGGGTTACCCGCTGTTATTGAGGAGTAACGGCCCAGCGGACCACCCAGGCTTGAGGCAG CAACGCGGGGTTACCCGCTGTTATTGAGGAGTGACGGCCCAGCGGACCACCCAGGCTTGAGGCAG A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:49942081..49942181 26863196 MeRIP-seq:(Medium) rs1462062948 Functional Loss SNV dbSNP153 33..33 33 - - - 61553 RMVar_ID_61553 Human_SNP_ID_431881727 m1A Human chr10 + 49964260 49964260 49964260 AATACTGAAATGAAATAATAAAATGAAATGCCAGGTGTGGTGGCACACTCCAGCCTGGGCAATAG AATACTGAAATGAAATAATAAAATGAAATGCCCGGTGTGGTGGCACACTCCAGCCTGGGCAATAG A C TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:49964175..49964259 26863196 MeRIP-seq:(Medium) rs138933322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8228746,Human_RBP_ID_22521248 RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 61554 RMVar_ID_61554 Human_SNP_ID_431881885 m1A Human chr10 + 49964694 49964694 49964694 GAAATGAATAATGAAATGCCAGGTGCAGTGGCACACTCCAGCCTGGGTGATAGAGCGAGTCTCTG GAAATGAATAATGAAATGCCAGGTGCAGTGGCGCACTCCAGCCTGGGTGATAGAGCGAGTCTCTG A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:49964653..49964775 26863196 MeRIP-seq:(Medium) rs1306048354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9443872,Human_RBP_ID_17647999,Human_RBP_ID_26317159 RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 61555 RMVar_ID_61555 Human_SNP_ID_431882228 m1A Human chr10 - 49965873 49965873 49965873 TATTGCCCAGGCTGGAGTGCGCCACCGCACCCAGCATTTCATTATTCCATTTTATCATTTAGTTT TATTGCCCAGGCTGGAGTGCGCCACCGCACCCGGCATTTCATTATTCCATTTTATCATTTAGTTT T C PARG Ensembl:ENSG00000227345 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:49965765..49965902 26863196 MeRIP-seq:(Medium) rs2490915 Functional Loss SNV dbSNP153 33..33 33 - - - 61556 RMVar_ID_61556 Human_SNP_ID_431910486 m1A Human chr10 + 50067724 50067724 50067724 CGCCGCTGCCTCGGGCCTTGGGGGGCAGCGCCACCCGGCCAACCCGCCTCTGCAGCGTTCCTGGC CGCCGCTGCCTCGGGCCTTGGGGGGCAGCGCCCCCCGGCCAACCCGCCTCTGCAGCGTTCCTGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:50067674..50067754 26863196 MeRIP-seq:(Medium) rs1280888835 Functional Loss SNV dbSNP153 33..33 33 - - - 61557 RMVar_ID_61557 Human_SNP_ID_431910625 m1A Human chr10 + 50067991 50067991 50067991 TCGGCGTGTGCTGGCAGCTTCGGAGCCCACCGAGCCGGGCGGCTAGGATGGTGAGGGCGCCGGGC TCGGCGTGTGCTGGCAGCTTCGGAGCCCACCGGGCCGGGCGGCTAGGATGGTGAGGGCGCCGGGC A G WASHC2A Ensembl:ENSG00000099290 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:50067944..50068059 26863196 MeRIP-seq:(Medium) rs1554874473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136275,Human_RBP_ID_8765304,Human_RBP_ID_9273812,Human_RBP_ID_18416112,Human_RBP_ID_22886802 Human_Splice_Rec_1132649,Human_Splice_Rec_1132703,Human_Splice_Rec_1132761,Human_Splice_Rec_1132817,Human_Splice_Rec_1132869 61558 RMVar_ID_61558 Human_SNP_ID_431910636 m1A Human chr10 - 50068010 50068010 50068010 CCAGGCCGGCCTCTCTCCTGCCCGGCGCCCTCACCATCCTAGCCGCCCGGCTCGGTGGGCTCCGA CCAGGCCGGCCTCTCTCCTGCCCGGCGCCCTCGCCATCCTAGCCGCCCGGCTCGGTGGGCTCCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:50067959..50068046;chr10:50067972..50068070;chr10:50067975..50068171;chr10:50067983..50068068 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs782001014 Functional Loss SNV dbSNP153 33..33 33 - - - 61559 RMVar_ID_61559 Human_SNP_ID_431963626 m1A Human chr10 + 50310010 50310010 50310010 CCCATCCAGTCCATCCTGCAAGCTGCTGCAAGAGTGATTTTTCTCTCTTCAAAGACAAATGACAC CCCATCCAGTCCATCCTGCAAGCTGCTGCAAGGGTGATTTTTCTCTCTTCAAAGACAAATGACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:50309893..50310107 26863196 MeRIP-seq:(Medium) rs1483411384 Functional Loss SNV dbSNP153 33..33 33 - - - 61560 RMVar_ID_61560 Human_SNP_ID_431981002 m1A Human chr10 - 50384374 50384371 50384375 GAAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGAGAAAGAAAGTAAGTTAGAAAAAGTTTAAAAAT GAAAGGAGAGAGAGAGAGAGAAAAAGAAAGA____AAGAAAGTAAGTTAGAAAAAGTTTAAAAAT TTCTC T SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:50384372..50384492 26863196 MeRIP-seq:(Medium) rs1016949343 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_22567458 RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186 61561 RMVar_ID_61561 Human_SNP_ID_431981003 m1A Human chr10 - 50384374 50384374 50384374 GAAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGAGAAAGAAAGTAAGTTAGAAAAAGTTTAAAAAT GAAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGGGAAAGAAAGTAAGTTAGAAAAAGTTTAAAAAT T C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:50384372..50384492 26863196 MeRIP-seq:(Medium) rs1447903791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22567458 RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186 61562 RMVar_ID_61562 Human_SNP_ID_431981008 m1A Human chr10 - 50384385 50384381 50384385 AAAGAAGGAAGGAAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGAGAAAGAAAGTAAGTTAGAAAA AAAGAAGGAAGGAAAGGAGAGAGAGAGAGAGA____GAAAGAGAGAAAGAAAGTAAGTTAGAAAA CTTTT C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:50384377..50384595 26863196 MeRIP-seq:(Medium) rs1171434602 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_22567458,Human_RBP_ID_24813324 RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186 61563 RMVar_ID_61563 Human_SNP_ID_431981011 m1A Human chr10 - 50384385 50384385 50384385 AAAGAAGGAAGGAAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGAGAAAGAAAGTAAGTTAGAAAA AAAGAAGGAAGGAAAGGAGAGAGAGAGAGAGAGAAAGAAAGAGAGAAAGAAAGTAAGTTAGAAAA T C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:50384377..50384595 26863196 MeRIP-seq:(Medium) rs985612375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22567458,Human_RBP_ID_24813324 RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186 61564 RMVar_ID_61564 Human_SNP_ID_431988586 m1A Human chr10 - 50418295 50418295 50418295 GCCGCCCGCCAGCTCCAGACGCCGGGCTCCGCAGCGCCGCTGTCCTAGCACCAGGGCCCGGCAAG GCCGCCCGCCAGCTCCAGACGCCGGGCTCCGCGGCGCCGCTGTCCTAGCACCAGGGCCCGGCAAG T C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:50418244..50418410;chr10:50418245..50418412 26863196 MeRIP-seq:(Medium) rs1157493044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136276 RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186 61565 RMVar_ID_61565 Human_SNP_ID_431988588 m1A Human chr10 + 50418300 50418300 50418300 CGGGCCCTGGTGCTAGGACAGCGGCGCTGCGGAGCCCGGCGTCTGGAGCTGGCGGGCGGCCGGAT CGGGCCCTGGTGCTAGGACAGCGGCGCTGCGGGGCCCGGCGTCTGGAGCTGGCGGGCGGCCGGAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:50418251..50418398 26863196 MeRIP-seq:(Medium) rs891002228 Functional Loss SNV dbSNP153 33..33 33 - - - 61566 RMVar_ID_61566 Human_SNP_ID_432062893 m1A Human chr10 - 50739985 50739985 50739985 CCCACTGCCGCCTACCCCAGCCGCAGCACCGAACCTGTTCACAATTGCGACTCCTCAGGTCCGCT CCCACTGCCGCCTACCCCAGCCGCAGCACCGAGCCTGTTCACAATTGCGACTCCTCAGGTCCGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:50739982..50740053 26863196 MeRIP-seq:(Medium) rs1353372193 Functional Loss SNV dbSNP153 33..33 33 - - - 61567 RMVar_ID_61567 Human_SNP_ID_432290158 m1A Human chr10 + 51697711 51697711 51697711 CAAATATTTTCTAAAACCTTTCAAGACGCTCCAGTGGATTTCTGGATTTGTTCCTTTAAAATCAG CAAATATTTTCTAAAACCTTTCAAGACGCTCCGGTGGATTTCTGGATTTGTTCCTTTAAAATCAG A G PRKG1 Ensembl:ENSG00000185532 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:51697662..51697860 32194978 MeRIP-seq:(Medium) rs771581979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71630,RMVar_hsa_circ_334612,RMVar_hsa_circ_63103 61568 RMVar_ID_61568 Human_SNP_ID_432290227 m1A Human chr10 - 51697948 51697948 51697948 CAAGGAGGAGGGATGCAGGGGGCAGGCATACAAGGAGTCAGTATACAAGGAGGAGGTATACAAGG CAAGGAGGAGGGATGCAGGGGGCAGGCATACATGGAGTCAGTATACAAGGAGGAGGTATACAAGG T A CSTF2T Ensembl:ENSG00000177613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:51697826..51698367 26863196 MeRIP-seq:(Medium) rs745971043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378397,Human_RBP_ID_3351939,Human_RBP_ID_4120966,Human_RBP_ID_5086611,Human_RBP_ID_5137854,Human_RBP_ID_5977514,Human_RBP_ID_8761200,Human_RBP_ID_27608203 Human_miRNA_ID_1005574 61569 RMVar_ID_61569 Human_SNP_ID_432290582 m1A Human chr10 + 51698848 51698848 51698848 CTTCTAGCCAAATGCTGAGGCTGAGGAGCTGGAGGATTCTGCTGGTTCAGCAGAACATTAGGTCC CTTCTAGCCAAATGCTGAGGCTGAGGAGCTGGGGGATTCTGCTGGTTCAGCAGAACATTAGGTCC A G PRKG1 Ensembl:ENSG00000185532 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:51698799..51698899 32194978 MeRIP-seq:(Medium) rs1030885581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71630,RMVar_hsa_circ_334612,RMVar_hsa_circ_63103 61570 RMVar_ID_61570 Human_SNP_ID_432290801 m1A Human chr10 - 51699478 51699478 51699478 TCACTGCGTTCCGTGTTCGTGGGGAACATTCCATATGAGGCAACTGAGGAGCAGTTAAAGGACAT TCACTGCGTTCCGTGTTCGTGGGGAACATTCCTTATGAGGCAACTGAGGAGCAGTTAAAGGACAT T A CSTF2T Ensembl:ENSG00000177613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:51699428..51699560 26863196 MeRIP-seq:(Medium) rs992215828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_983316,Human_RBP_ID_3351956,Human_RBP_ID_4121027,Human_RBP_ID_5977548,Human_RBP_ID_8056871,Human_RBP_ID_8761227,Human_RBP_ID_8989460,Human_RBP_ID_11372752,Human_RBP_ID_17227220,Human_RBP_ID_17778458 61571 RMVar_ID_61571 Human_SNP_ID_432290802 m1A Human chr10 - 51699478 51699478 51699478 TCACTGCGTTCCGTGTTCGTGGGGAACATTCCATATGAGGCAACTGAGGAGCAGTTAAAGGACAT TCACTGCGTTCCGTGTTCGTGGGGAACATTCCCTATGAGGCAACTGAGGAGCAGTTAAAGGACAT T G CSTF2T Ensembl:ENSG00000177613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:51699428..51699560 26863196 MeRIP-seq:(Medium) rs992215828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_983316,Human_RBP_ID_3351956,Human_RBP_ID_4121027,Human_RBP_ID_5977548,Human_RBP_ID_8056871,Human_RBP_ID_8761227,Human_RBP_ID_8989460,Human_RBP_ID_11372752,Human_RBP_ID_17227220,Human_RBP_ID_17778458 61572 RMVar_ID_61572 Human_SNP_ID_432290824 m1A Human chr10 - 51699553 51699553 51699553 AAGAATCCGCTATCGGCTGTCTGCACAACCGGAATCATGTCGAGTTTGGCGGTGAGAGACCCGGC AAGAATCCGCTATCGGCTGTCTGCACAACCGGCATCATGTCGAGTTTGGCGGTGAGAGACCCGGC T G CSTF2T Ensembl:ENSG00000177613 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:51699285..51699600 26863196 MeRIP-seq:(Medium) rs1210133051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1447193,Human_RBP_ID_4136278 61573 RMVar_ID_61573 Human_SNP_ID_433286639 m1A Human chr10 - 55599893 55599893 55599893 AGACAGCTAAACCCTGGTGTGGCCATTCATACAAGTCCCTACTTAGGGAACAAGTGATTATGCTA AGACAGCTAAACCCTGGTGTGGCCATTCATACGAGTCCCTACTTAGGGAACAAGTGATTATGCTA T C PCDH15 Ensembl:ENSG00000150275 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:55599854..55599975 26863196 MeRIP-seq:(Medium) rs1291841071 Functional Loss SNV dbSNP153 33..33 33 - - - 61574 RMVar_ID_61574 Human_SNP_ID_433474551 m1A Human chr10 + 56358658 56358652 56358658 TGGGGTTTATCATCTGGAAGATTCTCTGCCTCAGCCTCAGCCTCAGGGAACAACAGCTTACCCTG TGGGGTTTATCATCTGGAAGATTCTCT______GCCTCAGCCTCAGGGAACAACAGCTTACCCTG TGCCTCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:56358601..56358725 32194978 MeRIP-seq:(Medium) rs200951666 Functional Loss DEL dbSNP153 28..33 33 - - - 61575 RMVar_ID_61575 Human_SNP_ID_433474557 m1A Human chr10 + 56358658 56358658 56358658 TGGGGTTTATCATCTGGAAGATTCTCTGCCTCAGCCTCAGCCTCAGGGAACAACAGCTTACCCTG TGGGGTTTATCATCTGGAAGATTCTCTGCCTCGGCCTCAGCCTCAGGGAACAACAGCTTACCCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:56358601..56358725 32194978 MeRIP-seq:(Medium) rs1322433289 Functional Loss SNV dbSNP153 33..33 33 - - - 61576 RMVar_ID_61576 Human_SNP_ID_433474645 m1A Human chr10 - 56358891 56358889 56358891 GAGGTTTCTGCAGAGGTGAGGGAGCGTAAGACAGGGACTCAGCAGGAGCTTGACAGGGTGTTTCA GAGGTTTCTGCAGAGGTGAGGGAGCGTAAGAC__GGACTCAGCAGGAGCTTGACAGGGTGTTTCA CCT C ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:56358793..56358891 26863196 MeRIP-seq:(Medium) rs755393132 Functional Loss DEL dbSNP153,HGVD 33..34 33 - - - Human_RBP_ID_862331,Human_RBP_ID_4121763,Human_RBP_ID_5339165,Human_RBP_ID_5979884,Human_RBP_ID_9360346,Human_RBP_ID_22029769,Human_RBP_ID_22886724,Human_RBP_ID_26317172 Human_Splice_Rec_1135716,Human_Splice_Rec_1135717,Human_Splice_Rec_1135728,Human_Splice_Rec_1135729,Human_Splice_Rec_1135744,Human_Splice_Rec_1135745,Human_Splice_Rec_1135752,Human_Splice_Rec_1135753,Human_Splice_Rec_1135764,Human_Splice_Rec_1135774,Human_Splice_Rec_1135775,Human_Splice_Rec_1135790,Human_Splice_Rec_1135802,Human_Splice_Rec_1135812,Human_Splice_Rec_1135813 Human_miRNA_ID_2210381,Human_miRNA_ID_2444043,Human_miRNA_ID_2444044,Human_miRNA_ID_2511930,Human_miRNA_ID_3054748 RMVar_hsa_circ_143483,RMVar_hsa_circ_86937,RMVar_hsa_circ_143482,RMVar_hsa_circ_116254 61577 RMVar_ID_61577 Human_SNP_ID_433474647 m1A Human chr10 - 56358891 56358891 56358891 GAGGTTTCTGCAGAGGTGAGGGAGCGTAAGACAGGGACTCAGCAGGAGCTTGACAGGGTGTTTCA GAGGTTTCTGCAGAGGTGAGGGAGCGTAAGACCGGGACTCAGCAGGAGCTTGACAGGGTGTTTCA T G ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:56358793..56358891 26863196 MeRIP-seq:(Medium) rs1467258355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862331,Human_RBP_ID_4121763,Human_RBP_ID_5339165,Human_RBP_ID_5979884,Human_RBP_ID_9360346,Human_RBP_ID_22029769,Human_RBP_ID_22886724,Human_RBP_ID_26317172 Human_Splice_Rec_1135716,Human_Splice_Rec_1135717,Human_Splice_Rec_1135728,Human_Splice_Rec_1135729,Human_Splice_Rec_1135744,Human_Splice_Rec_1135745,Human_Splice_Rec_1135752,Human_Splice_Rec_1135753,Human_Splice_Rec_1135764,Human_Splice_Rec_1135774,Human_Splice_Rec_1135775,Human_Splice_Rec_1135790,Human_Splice_Rec_1135802,Human_Splice_Rec_1135812,Human_Splice_Rec_1135813 Human_miRNA_ID_2210381,Human_miRNA_ID_2444043,Human_miRNA_ID_2444044,Human_miRNA_ID_2511930,Human_miRNA_ID_3054748 RMVar_hsa_circ_143483,RMVar_hsa_circ_86937,RMVar_hsa_circ_143482,RMVar_hsa_circ_116254 61578 RMVar_ID_61578 Human_SNP_ID_433474667 m1A Human chr10 - 56358931 56358931 56358931 TGCTCACTCCTGGCAGGAGAAGCATCTGCAGCATCTGGCGGAGGTTTCTGCAGAGGTGAGGGAGC TGCTCACTCCTGGCAGGAGAAGCATCTGCAGCTTCTGGCGGAGGTTTCTGCAGAGGTGAGGGAGC T A ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:56358801..56358950 32194978 MeRIP-seq:(Medium) rs1310734373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861188,Human_RBP_ID_3352457,Human_RBP_ID_3938253,Human_RBP_ID_4142200,Human_RBP_ID_17778918,Human_RBP_ID_26317172 Human_Splice_Rec_1135716,Human_Splice_Rec_1135728,Human_Splice_Rec_1135744,Human_Splice_Rec_1135752,Human_Splice_Rec_1135764,Human_Splice_Rec_1135765,Human_Splice_Rec_1135774,Human_Splice_Rec_1135790,Human_Splice_Rec_1135791,Human_Splice_Rec_1135802,Human_Splice_Rec_1135803,Human_Splice_Rec_1135812 RMVar_hsa_circ_143483,RMVar_hsa_circ_86937,RMVar_hsa_circ_143482,RMVar_hsa_circ_116254 61579 RMVar_ID_61579 Human_SNP_ID_433474830 m1A Human chr10 - 56359527 56359527 56359527 TGGTCTTTCTCCCTTGCTTATCTGTAGAAACAAATGGCCATGGAGAAACGCAGAGCAGTCCAGAA TGGTCTTTCTCCCTTGCTTATCTGTAGAAACAGATGGCCATGGAGAAACGCAGAGCAGTCCAGAA T C ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:56359476..56359550 32194978 MeRIP-seq:(Medium) rs373707810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378810,Human_RBP_ID_983450,Human_RBP_ID_1767715,Human_RBP_ID_3352459,Human_RBP_ID_4121767,Human_RBP_ID_11376467,Human_RBP_ID_17778920,Human_RBP_ID_18595179 Human_Splice_Rec_1135714,Human_Splice_Rec_1135715,Human_Splice_Rec_1135726,Human_Splice_Rec_1135727,Human_Splice_Rec_1135742,Human_Splice_Rec_1135743,Human_Splice_Rec_1135750,Human_Splice_Rec_1135751,Human_Splice_Rec_1135762,Human_Splice_Rec_1135763,Human_Splice_Rec_1135772,Human_Splice_Rec_1135773,Human_Splice_Rec_1135788,Human_Splice_Rec_1135789,Human_Splice_Rec_1135800,Human_Splice_Rec_1135801,Human_Splice_Rec_1135810,Human_Splice_Rec_1135811 RMVar_hsa_circ_86937,RMVar_hsa_circ_143482 61580 RMVar_ID_61580 Human_SNP_ID_433474926 m1A Human chr10 - 56359852 56359852 56359852 TCATGTACTCATTCCTGGTGGCTCATCTCAGGACAGAAGGCAATTGCAGCTAAGGAACAATGGAA TCATGTACTCATTCCTGGTGGCTCATCTCAGGTCAGAAGGCAATTGCAGCTAAGGAACAATGGAA T A ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:56359801..56359920 26863196 MeRIP-seq:(Medium) rs1042964324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1447519,Human_RBP_ID_5339516,Human_RBP_ID_8335613,Human_RBP_ID_9360348,Human_RBP_ID_11376468,Human_RBP_ID_18431797,Human_RBP_ID_19452751,Human_RBP_ID_22536605,Human_RBP_ID_22639336,Human_RBP_ID_22735789,Human_RBP_ID_22882538,Human_RBP_ID_24816859,Human_RBP_ID_26316295 Human_Splice_Rec_1135712,Human_Splice_Rec_1135740,Human_Splice_Rec_1135760,Human_Splice_Rec_1135786,Human_Splice_Rec_1135798,Human_Splice_Rec_1135808 RMVar_hsa_circ_86937,RMVar_hsa_circ_143482 61581 RMVar_ID_61581 Human_SNP_ID_433475113 m1A Human chr10 + 56360350 56360350 56360350 GCTGGCAGTTCTGCCTCCTCCTGCAGGCCTACAGGTTCCAAGATGCCTGCCACCTCAGCCAGGAC GCTGGCAGTTCTGCCTCCTCCTGCAGGCCTACGGGTTCCAAGATGCCTGCCACCTCAGCCAGGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:56360301..56360400 32194978 MeRIP-seq:(Medium) rs748110307 Functional Loss SNV dbSNP153 33..33 33 - - - 61582 RMVar_ID_61582 Human_SNP_ID_433475396 m1A Human chr10 - 56361221 56361215 56361221 ACTCGGCGCCTGGAAAGATGGAGGCAGCGGAGACAGAGGCGGAAGCTGCAGCCCTAGAGTAAGTG ACTCGGCGCCTGGAAAGATGGAGGCAGCGGAG______GCGGAAGCTGCAGCCCTAGAGTAAGTG CCTCTGT C ZWINT Ensembl:ENSG00000122952 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:56360251..56361275 26863196 MeRIP-seq:(Medium) rs776857505 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_225209,Human_RBP_ID_1447532,Human_RBP_ID_4142212,Human_RBP_ID_18970758,Human_RBP_ID_22886726,Human_RBP_ID_26316298 Human_Splice_Rec_1135707,Human_Splice_Rec_1135723,Human_Splice_Rec_1135735,Human_Splice_Rec_1135757,Human_Splice_Rec_1135781 RMVar_hsa_circ_86937,RMVar_hsa_circ_143482 61583 RMVar_ID_61583 Human_SNP_ID_433958319 m1A Human chr10 + 58267637 58267637 58267637 TTGCCATAACGGAGAGCAGAAGCGGTAACGGCAGCGAGAGTAGGAAAAAAAATAGGGCGAGGGAG TTGCCATAACGGAGAGCAGAAGCGGTAACGGCGGCGAGAGTAGGAAAAAAAATAGGGCGAGGGAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:58267540..58267721 26863196 MeRIP-seq:(Medium) rs200036307 Functional Loss SNV dbSNP153 33..33 33 - - - 61584 RMVar_ID_61584 Human_SNP_ID_433958373 m1A Human chr10 - 58267795 58267795 58267795 AGCCGGGAGCCGCGTTCCGCCGAGAGTTGGGCAGAGGAGCGCCCGCGCCCCGGCGGCGTCATGGG AGCCGGGAGCCGCGTTCCGCCGAGAGTTGGGCGGAGGAGCGCCCGCGCCCCGGCGGCGTCATGGG T C IPMK Ensembl:ENSG00000151151 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:58267744..58267929 26863196 MeRIP-seq:(Medium) rs531493014 Functional Loss SNV dbSNP153 33..33 33 - - - 61585 RMVar_ID_61585 Human_SNP_ID_433958850 m1A Human chr10 - 58269230 58269220 58269230 TTGCAAGGCGTGTGCACTAGGATACCGAGCTCAAACGGGTTCGCGCGGCCGGCGAGAGTAAAGGT TTGCAAGGCGTGTGCACTAGGATACCGAGCTC__________GCGCGGCCGGCGAGAGTAAAGGT CGAACCCGTTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:58269155..58273434 32194978 MeRIP-seq:(Medium) rs1301122689 Functional Loss DEL dbSNP153 33..42 33 - - - 61586 RMVar_ID_61586 Human_SNP_ID_433958903 m1A Human chr10 - 58269306 58269306 58269306 CACCAGCCTCACCCGCTCCCAGGCCCCACTTCACCTCGTACGCTGGAACTGGAAGTCAGACTCAT CACCAGCCTCACCCGCTCCCAGGCCCCACTTCCCCTCGTACGCTGGAACTGGAAGTCAGACTCAT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:58269277..58269403 26863196 MeRIP-seq:(Medium) rs1166781182 Functional Loss SNV dbSNP153 33..33 33 - - - 61587 RMVar_ID_61587 Human_SNP_ID_433974056 m1A Human chr10 + 58335049 58335049 58335049 CACACTCGCGCTCGGGCGCACACGGAGCAGGGACCGGCGCCCGGAGCGAGCCAGGGAGCGGCTAA CACACTCGCGCTCGGGCGCACACGGAGCAGGGGCCGGCGCCCGGAGCGAGCCAGGGAGCGGCTAA A G UBE2D1 Ensembl:ENSG00000072401 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:58335001..58335224 26863196 MeRIP-seq:(Medium) rs556464787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4122065,Human_RBP_ID_5459755 61588 RMVar_ID_61588 Human_SNP_ID_433974069 m1A Human chr10 + 58335069 58335069 58335069 CACGGAGCAGGGACCGGCGCCCGGAGCGAGCCAGGGAGCGGCTAACCGGGGACCCACCGCGCGGA CACGGAGCAGGGACCGGCGCCCGGAGCGAGCCTGGGAGCGGCTAACCGGGGACCCACCGCGCGGA A T UBE2D1 Ensembl:ENSG00000072401 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:58335018..58335193 26863196 MeRIP-seq:(Medium) rs1230370760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4122068,Human_RBP_ID_5459755 61589 RMVar_ID_61589 Human_SNP_ID_433985213 m1A Human chr10 - 58385520 58385520 58385520 GCCATCGCTCCGGTGGATGAGGCAGTGACCCGACCCCAATCTCGGAGAGCCTCCTGGCAATACAC GCCATCGCTCCGGTGGATGAGGCAGTGACCCGGCCCCAATCTCGGAGAGCCTCCTGGCAATACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:58385469..58385563 26863196 MeRIP-seq:(Medium) rs1224231975 Functional Loss SNV dbSNP153 33..33 33 - - - 61590 RMVar_ID_61590 Human_SNP_ID_434015535 m1A Human chr10 - 58513017 58512996 58513017 CGCGGCGCTAGCTCGTCCCCCTGCAGCCGCCGACGCCACCGCCAACGCCGCCGCCGCCACTGAGC CGCGGCGCTAGCTCGTCCCCCTGCAGCCGCCG_____________________CCGCCACTGAGC GCGGCGGCGTTGGCGGTGGCGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr10:58512977..58513192;chr10:58512834..58650110 26863196 MeRIP-seq:(Medium) rs1286369426 Functional Loss DEL dbSNP153 33..53 33 - - - 61591 RMVar_ID_61591 Human_SNP_ID_434015540 m1A Human chr10 - 58513012 58513012 58513012 CGCTAGCTCGTCCCCCTGCAGCCGCCGACGCCACCGCCAACGCCGCCGCCGCCACTGAGCCCCCG CGCTAGCTCGTCCCCCTGCAGCCGCCGACGCCGCCGCCAACGCCGCCGCCGCCACTGAGCCCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:58512830..58513281 26863196 MeRIP-seq:(Medium) rs1490508573 Functional Loss SNV dbSNP153 33..33 33 - - - 61592 RMVar_ID_61592 Human_SNP_ID_434015545 m1A Human chr10 - 58513017 58513017 58513017 CGCGGCGCTAGCTCGTCCCCCTGCAGCCGCCGACGCCACCGCCAACGCCGCCGCCGCCACTGAGC CGCGGCGCTAGCTCGTCCCCCTGCAGCCGCCGCCGCCACCGCCAACGCCGCCGCCGCCACTGAGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr10:58512977..58513192;chr10:58512834..58650110 26863196 MeRIP-seq:(Medium) rs1228435081 Functional Loss SNV dbSNP153 33..33 33 - - - 61593 RMVar_ID_61593 Human_SNP_ID_434046297 m1A Human chr10 - 58637849 58637849 58637849 ACAGTGCTTAGTTACTAGATCCCCTCTGGTCCACCATGCCTGTCCCAATTTATAAGTTATGCCAC ACAGTGCTTAGTTACTAGATCCCCTCTGGTCCCCCATGCCTGTCCCAATTTATAAGTTATGCCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:58637834..58638010 26863196 MeRIP-seq:(Medium) rs1027841545 Functional Loss SNV dbSNP153 33..33 33 - - - 61594 RMVar_ID_61594 Human_SNP_ID_434200815 m1A Human chr10 + 59284826 59284826 59284826 CCGAAACCTCCCAGCCTACTCCACACATACCCATGCACACCCACCTCACACACACCCACATCCAA CCGAAACCTCCCAGCCTACTCCACACATACCCTTGCACACCCACCTCACACACACCCACATCCAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:59284777..59284947 26863196 MeRIP-seq:(Medium) rs1480989881 Functional Loss SNV dbSNP153 33..33 33 - - - 61595 RMVar_ID_61595 Human_SNP_ID_434304402 m1A Human chr10 - 59709801 59709801 59709801 CCGCAAAGAGAGACAAGGGAGAAAAAGACAGCAGGGAAAACCCCGGGGAGGAGAAGGCGAAAGAG CCGCAAAGAGAGACAAGGGAGAAAAAGACAGCGGGGAAAACCCCGGGGAGGAGAAGGCGAAAGAG T C SLC16A9 Ensembl:ENSG00000165449 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:59709554..59709859 26863196 MeRIP-seq:(Medium) rs1362158146 Functional Loss SNV dbSNP153 33..33 33 - - - 61596 RMVar_ID_61596 Human_SNP_ID_434304403 m1A Human chr10 - 59709801 59709801 59709801 CCGCAAAGAGAGACAAGGGAGAAAAAGACAGCAGGGAAAACCCCGGGGAGGAGAAGGCGAAAGAG CCGCAAAGAGAGACAAGGGAGAAAAAGACAGCCGGGAAAACCCCGGGGAGGAGAAGGCGAAAGAG T G SLC16A9 Ensembl:ENSG00000165449 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:59709554..59709859 26863196 MeRIP-seq:(Medium) rs1362158146 Functional Loss SNV dbSNP153 33..33 33 - - - 61597 RMVar_ID_61597 Human_SNP_ID_434325173 m1A Human chr10 - 59792958 59792958 59792958 CCACGGTCCCCTCAGCAGCCACCTCGCAGCCTACTCCTTCGCAACATTCGGCGCACCCCTCCTCC CCACGGTCCCCTCAGCAGCCACCTCGCAGCCTTCTCCTTCGCAACATTCGGCGCACCCCTCCTCC T A CCDC6 Ensembl:ENSG00000108091 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:59792907..59793100 26863196 MeRIP-seq:(Medium) rs1378757870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5982427,Human_RBP_ID_17227487,Human_RBP_ID_17344085,Human_RBP_ID_17460140,Human_RBP_ID_17779493 61598 RMVar_ID_61598 Human_SNP_ID_434325182 m1A Human chr10 + 59792984 59792984 59792984 AAGGAGTAGGCTGCGAGGTGGCTGCTGAGGGGACCGTGGGCTGCATGGGTGGCGGAGGTGGAGGC AAGGAGTAGGCTGCGAGGTGGCTGCTGAGGGGGCCGTGGGCTGCATGGGTGGCGGAGGTGGAGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:59792917..59793076 26863196 MeRIP-seq:(Medium) rs1362746781 Functional Loss SNV dbSNP153 33..33 33 - - - 61599 RMVar_ID_61599 Human_SNP_ID_434343659 m1A Human chr10 - 59868381 59868381 59868381 TATCTGCATGGCCCAGTGGTGGTGGGCTGGGCAGGAAAATCACACGGTCCAGTGGTGGTGGGCTT TATCTGCATGGCCCAGTGGTGGTGGGCTGGGCCGGAAAATCACACGGTCCAGTGGTGGTGGGCTT T G CCDC6 Ensembl:ENSG00000108091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:59868377..59868488 26863196 MeRIP-seq:(Medium) rs1331127107 Functional Loss SNV dbSNP153 33..33 33 - - - 61600 RMVar_ID_61600 Human_SNP_ID_572012269 m1A Human chr15 - 30626149 30626149 30626149 GCCGTTAGCCTCATGCTTCCGCCCCCAGCTCCACTGCAGACACCCGGAGCCACCACGGGGGGGTC GCCGTTAGCCTCATGCTTCCGCCCCCAGCTCCTCTGCAGACACCCGGAGCCACCACGGGGGGGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:30626101..30626200;chr15:30626088..30626208 26863196 MeRIP-seq:(Medium) rs947795346 Functional Loss SNV dbSNP153 33..33 33 - - - 61601 RMVar_ID_61601 Human_SNP_ID_572012462 m1A Human chr15 + 30626810 30626810 30626810 GTCAGGACCTGCATCCTGCCTCAGAGTTATCGACGTATCCGGAATGTGGGATCAGAGGCTGGTGA GTCAGGACCTGCATCCTGCCTCAGAGTTATCGGCGTATCCGGAATGTGGGATCAGAGGCTGGTGA A G ARHGAP11B,ARHGAP11B:2 Ensembl:ENSG00000285077,Ensembl:ENSG00000284906 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:30626769..30626836 26863196 MeRIP-seq:(Medium) rs1357715694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9370655,Human_RBP_ID_18661144,Human_RBP_ID_18982000,Human_RBP_ID_23647871 61602 RMVar_ID_61602 Human_SNP_ID_572018429 m1A Human chr15 + 30650404 30650404 30650404 AGTTAGGGAAGGGTGAGGAAGAGGAGTTGGTCAACAGGAAGCAGGTAGTTGGTTAGGCAATTGTG AGTTAGGGAAGGGTGAGGAAGAGGAGTTGGTCGACAGGAAGCAGGTAGTTGGTTAGGCAATTGTG A G AC091057.6,ARHGAP11B Ensembl:ENSG00000285035,Ensembl:ENSG00000284906 Pseudogene,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:30650366..30650443;chr15:30650367..30650474 26863196 MeRIP-seq:(Medium) rs1342526841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251691,Human_RBP_ID_9816153,Human_RBP_ID_22579048,Human_RBP_ID_23273552 RMVar_hsa_circ_170439,RMVar_hsa_circ_371621 61603 RMVar_ID_61603 Human_SNP_ID_572027280 m1A Human chr15 + 30685889 30685889 30685889 AGGAAGTAGTTTATATCAGAGAGGAACAGGATATCACATCATTCAGAGCATTGTAAGATGTGGTA AGGAAGTAGTTTATATCAGAGAGGAACAGGATGTCACATCATTCAGAGCATTGTAAGATGTGGTA A G AC091057.6,AC091057.1 Ensembl:ENSG00000285035,Ensembl:ENSG00000187951 Pseudogene,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:30685855..30685983 26863196 MeRIP-seq:(Medium) rs1469956639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12486764 RMVar_hsa_circ_170440,RMVar_hsa_circ_170439,RMVar_hsa_circ_371621,RMVar_hsa_circ_377077 61604 RMVar_ID_61604 Human_SNP_ID_572046917 m1A Human chr15 + 30768292 30768292 30768292 GTTGCAAGTCAAAATTACTCCTTGATCCGTGGAGTACAGAATGGATGTTGTATTAGCAGACATGA GTTGCAAGTCAAAATTACTCCTTGATCCGTGGCGTACAGAATGGATGTTGTATTAGCAGACATGA A C AC091057.1 Ensembl:ENSG00000187951 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:30768249..30768352 26863196 MeRIP-seq:(Medium) rs558986343 Functional Loss SNV dbSNP153 33..33 33 - - - 61605 RMVar_ID_61605 Human_SNP_ID_572047593 m1A Human chr15 - 30770980 30770980 30770980 GCATATACGTCCCTGCCAGCACGCCACGGCGCATGCTCTGTGTTCTGCCCGGATGTTCTCCACCC GCATATACGTCCCTGCCAGCACGCCACGGCGCGTGCTCTGTGTTCTGCCCGGATGTTCTCCACCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:30770874..30771047 26863196 MeRIP-seq:(Medium) rs1321391870 Functional Loss SNV dbSNP153 33..33 33 - - - 61606 RMVar_ID_61606 Human_SNP_ID_572083080 m1A Human chr15 + 30904473 30904473 30904473 TTTCAGAGTTCGCTTTTCCCCTTGCTGAATTCATAAAAATGTTTTTAATTTATATGTGTTTCTTC TTTCAGAGTTCGCTTTTCCCCTTGCTGAATTCGTAAAAATGTTTTTAATTTATATGTGTTTCTTC A G FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:30904470..30904586 26863196 MeRIP-seq:(Medium) rs1361194757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1277893 61607 RMVar_ID_61607 Human_SNP_ID_572083081 m1A Human chr15 + 30904473 30904473 30904473 TTTCAGAGTTCGCTTTTCCCCTTGCTGAATTCATAAAAATGTTTTTAATTTATATGTGTTTCTTC TTTCAGAGTTCGCTTTTCCCCTTGCTGAATTCTTAAAAATGTTTTTAATTTATATGTGTTTCTTC A T FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:30904470..30904586 26863196 MeRIP-seq:(Medium) rs1361194757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1277893 61608 RMVar_ID_61608 Human_SNP_ID_572086442 m1A Human chr15 + 30917078 30917078 30917078 GATGTGGGGGTGGACAGGACTGGGTTGTTGGTAGCGGCAGTGGAGAGAAGTGAATGTGTATGAGG GATGTGGGGGTGGACAGGACTGGGTTGTTGGTGGCGGCAGTGGAGAGAAGTGAATGTGTATGAGG A G FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:30916989..30917253 26863196 MeRIP-seq:(Medium) rs1222733668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815362 RMVar_hsa_circ_47541,RMVar_hsa_circ_115269,RMVar_hsa_circ_170443,RMVar_hsa_circ_296228,RMVar_hsa_circ_370996,RMVar_hsa_circ_48432,RMVar_hsa_circ_170444,RMVar_hsa_circ_170445,RMVar_hsa_circ_289685,RMVar_hsa_circ_66994,RMVar_hsa_circ_170448 61609 RMVar_ID_61609 Human_SNP_ID_572165902 m1A Human chr15 - 31216301 31216301 31216301 TCCCACCGCTCCTTCCTCTCCTCCTTTCCCGCACCCCTCCTTTCTTTCTCGCTCATCTCTCTGCC TCCCACCGCTCCTTCCTCTCCTCCTTTCCCGCCCCCCTCCTTTCTTTCTCGCTCATCTCTCTGCC T G LOC283710 RNACentral:URS0000D5C33D lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:31216299..31216458 26863196 MeRIP-seq:(Medium) rs1259724907 Functional Loss SNV dbSNP153 33..33 33 - - - 61610 RMVar_ID_61610 Human_SNP_ID_572165910 m1A Human chr15 + 31216333 31216330 31216333 TGCGGGAAAGGAGGAGAGGAAGGAGCGGTGGGAGGAGGAGGAGGGGTGCGGGAGAGAAGGGCTGA TGCGGGAAAGGAGGAGAGGAAGGAGCGGTG___GGAGGAGGAGGGGTGCGGGAGAGAAGGGCTGA GGGA G LINC02352 Ensembl:ENSG00000259448 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:31216282..31216404 26863196 MeRIP-seq:(Medium) rs200060027 Functional Loss DEL dbSNP153 31..33 33 - - - 61611 RMVar_ID_61611 Human_SNP_ID_572165918 m1A Human chr15 + 31216353 31216353 31216353 AGGAGCGGTGGGAGGAGGAGGAGGGGTGCGGGAGAGAAGGGCTGAGGGAGAGGCGGAGGGAAACC AGGAGCGGTGGGAGGAGGAGGAGGGGTGCGGGGGAGAAGGGCTGAGGGAGAGGCGGAGGGAAACC A G LINC02352 Ensembl:ENSG00000259448 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:31216303..31216550 26863196 MeRIP-seq:(Medium) rs891498642 Functional Loss SNV dbSNP153 33..33 33 - - - 61612 RMVar_ID_61612 Human_SNP_ID_572195846 m1A Human chr15 + 31327715 31327715 31327715 CGCCGACCTCGAGTCCCCGCAGAGGAAGCACAAGTGCCACTACGCGGGCTGCGAGAAAGTTTACG CGCCGACCTCGAGTCCCCGCAGAGGAAGCACAGGTGCCACTACGCGGGCTGCGAGAAAGTTTACG A G KLF13 Ensembl:ENSG00000169926 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:31327598..31327717 26863196 MeRIP-seq:(Medium) rs757068968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1577129,Human_Splice_Rec_1577131 Human_miRNA_ID_2237356 RMVar_hsa_circ_127198,RMVar_hsa_circ_170460 61613 RMVar_ID_61613 Human_SNP_ID_572201717 m1A Human chr15 + 31346820 31346820 31346820 TCCTGCCGGCCATAGGTGGGCTATTGGCCTGCAGGCCAGGTTCCTGCCTGCCACCACTCTGCACC TCCTGCCGGCCATAGGTGGGCTATTGGCCTGCGGGCCAGGTTCCTGCCTGCCACCACTCTGCACC A G KLF13 Ensembl:ENSG00000169926 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:31346812..31347066 26863196 MeRIP-seq:(Medium) rs554685300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127198,RMVar_hsa_circ_170460 61614 RMVar_ID_61614 Human_SNP_ID_572332169 m1A Human chr15 - 31870670 31870670 31870670 GCGGAGCGGAGCGCGGGAGGAGGCGGGGGAGGAGAGGCCACCGGGACCGCGAGCGGCAGCTGGGG GCGGAGCGGAGCGCGGGAGGAGGCGGGGGAGGTGAGGCCACCGGGACCGCGAGCGGCAGCTGGGG T A OTUD7A Ensembl:ENSG00000169918 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:31870543..31870672 26863196 MeRIP-seq:(Medium) rs1006548456 Functional Loss SNV dbSNP153 33..33 33 - - - 61615 RMVar_ID_61615 Human_SNP_ID_572482544 m1A Human chr15 + 32615536 32615536 32615536 GACCCCCCCGTGGTGGCTCTGGGTGTCTGCGGAGGAGCTGGGGGCGGAAGCATGAGGCTAACGGC GACCCCCCCGTGGTGGCTCTGGGTGTCTGCGGGGGAGCTGGGGGCGGAAGCATGAGGCTAACGGC A G ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:32615476..32615629;chr15:32615476..32615606 26863196 MeRIP-seq:(Medium) rs1262195817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342536,Human_RBP_ID_18418329 Human_Splice_Rec_1577995 RMVar_hsa_circ_105871,RMVar_hsa_circ_170474 61616 RMVar_ID_61616 Human_SNP_ID_572482545 m1A Human chr15 + 32615536 32615536 32615536 GACCCCCCCGTGGTGGCTCTGGGTGTCTGCGGAGGAGCTGGGGGCGGAAGCATGAGGCTAACGGC GACCCCCCCGTGGTGGCTCTGGGTGTCTGCGGTGGAGCTGGGGGCGGAAGCATGAGGCTAACGGC A T ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:32615476..32615629;chr15:32615476..32615606 26863196 MeRIP-seq:(Medium) rs1262195817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342536,Human_RBP_ID_18418329 Human_Splice_Rec_1577995 RMVar_hsa_circ_105871,RMVar_hsa_circ_170474 61617 RMVar_ID_61617 Human_SNP_ID_572482681 m1A Human chr15 + 32615969 32615969 32615969 TGGGTGACCAGAAAGAAGGTCGGTGTAAGTGAAGGAAGAGTGAGGTGTGGCTGGATCAAAGGGCT TGGGTGACCAGAAAGAAGGTCGGTGTAAGTGATGGAAGAGTGAGGTGTGGCTGGATCAAAGGGCT A T ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:32615476..32616076 26863196 MeRIP-seq:(Medium) rs1366522165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6417503,Human_RBP_ID_12488142,Human_RBP_ID_23648244,Human_RBP_ID_26326447 RMVar_hsa_circ_101200,RMVar_hsa_circ_105871,RMVar_hsa_circ_170474,RMVar_hsa_circ_66213,RMVar_hsa_circ_170475 61618 RMVar_ID_61618 Human_SNP_ID_572482686 m1A Human chr15 + 32615991 32615991 32615991 GTGTAAGTGAAGGAAGAGTGAGGTGTGGCTGGATCAAAGGGCTAAGAGAAGCGGGTCTGTGTAAG GTGTAAGTGAAGGAAGAGTGAGGTGTGGCTGGGTCAAAGGGCTAAGAGAAGCGGGTCTGTGTAAG A G ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:32615895..32616019 26863196 MeRIP-seq:(Medium) rs1251244523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12488143,Human_RBP_ID_23648244 RMVar_hsa_circ_101200,RMVar_hsa_circ_105871,RMVar_hsa_circ_170474,RMVar_hsa_circ_66213,RMVar_hsa_circ_170475 61619 RMVar_ID_61619 Human_SNP_ID_572484834 m1A Human chr15 - 32623288 32623288 32623288 CTTCTCCAAGGCCCATCTTTTTACTTCTAACAACTCCAATGTGCACACTAAATTTTATCTTTCTC CTTCTCCAAGGCCCATCTTTTTACTTCTAACAGCTCCAATGTGCACACTAAATTTTATCTTTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:32623227..32623333 26863196 MeRIP-seq:(Medium) rs1350295200 Functional Loss SNV dbSNP153 33..33 33 - - - 61620 RMVar_ID_61620 Human_SNP_ID_572492112 m1A Human chr15 + 32652276 32652276 32652276 GAGCCGGCTCTGGGGAGTAGTGGGGGCCCACCATACCTGCAGGGCATTGAGGGGATAAACAAGGA GAGCCGGCTCTGGGGAGTAGTGGGGGCCCACCCTACCTGCAGGGCATTGAGGGGATAAACAAGGA A C SCG5 Ensembl:ENSG00000166922 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:32652251..32652319 26863196 MeRIP-seq:(Medium) rs867308670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376146,RMVar_hsa_circ_96230,RMVar_hsa_circ_170478,RMVar_hsa_circ_170479 61621 RMVar_ID_61621 Human_SNP_ID_572492113 m1A Human chr15 + 32652276 32652276 32652276 GAGCCGGCTCTGGGGAGTAGTGGGGGCCCACCATACCTGCAGGGCATTGAGGGGATAAACAAGGA GAGCCGGCTCTGGGGAGTAGTGGGGGCCCACCGTACCTGCAGGGCATTGAGGGGATAAACAAGGA A G SCG5 Ensembl:ENSG00000166922 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:32652251..32652319 26863196 MeRIP-seq:(Medium) rs867308670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376146,RMVar_hsa_circ_96230,RMVar_hsa_circ_170478,RMVar_hsa_circ_170479 61622 RMVar_ID_61622 Human_SNP_ID_572512218 m1A Human chr15 - 32733393 32733393 32733393 TTAACGAAATTGCATTCTTGTGGCAGAGTTAAAACAACAAGAGAAATTCAGTGTTTGCTGGTTCT TTAACGAAATTGCATTCTTGTGGCAGAGTTAAGACAACAAGAGAAATTCAGTGTTTGCTGGTTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:32733342..32733493 32194978 MeRIP-seq:(Medium) rs567560278 Functional Loss SNV dbSNP153 33..33 33 - - - 61623 RMVar_ID_61623 Human_SNP_ID_572862620 m1A Human chr15 - 33997653 33997653 33997653 GATGAGGGGCAGTAAAAAGATATTGGGATCACAGGACTACAGATTTTTTCAGGGCAGAAGGATTA GATGAGGGGCAGTAAAAAGATATTGGGATCACTGGACTACAGATTTTTTCAGGGCAGAAGGATTA T A AVEN Ensembl:ENSG00000169857 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:33997651..33997749 26863196 MeRIP-seq:(Medium) rs754228912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12489388 RMVar_hsa_circ_170517,RMVar_hsa_circ_100574,RMVar_hsa_circ_170516,RMVar_hsa_circ_84374 61624 RMVar_ID_61624 Human_SNP_ID_572862691 m1A Human chr15 + 33997984 33997984 33997984 CCTACTTGGAAAATAGGAAACTATACTTTCCCACTTCCTTGACAACTATTTCTTACCTTCTGCTC CCTACTTGGAAAATAGGAAACTATACTTTCCCGCTTCCTTGACAACTATTTCTTACCTTCTGCTC A G CHRM5 Ensembl:ENSG00000184984 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:33997975..33998123 26863196 MeRIP-seq:(Medium) rs1310983033 Functional Loss SNV dbSNP153 33..33 33 - - - 61625 RMVar_ID_61625 Human_SNP_ID_572872736 m1A Human chr15 - 34038824 34038824 34038824 GAGGCCGAGGAGGAGGAGGCGCCCCGCGAGGCAGCCGCCGGGAGCCGGGAGGCTGGGGCGCAGGG GAGGCCGAGGAGGAGGAGGCGCCCCGCGAGGCGGCCGCCGGGAGCCGGGAGGCTGGGGCGCAGGG T C AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:34003165..34038981 26863410 MeRIP-seq:(Medium) rs1251130548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1579741 61626 RMVar_ID_61626 Human_SNP_ID_572872754 m1A Human chr15 + 34038882 34038876 34038882 CGGCCTCCGCGAGCGCCGCGGAAGCCCCGGCCACGGCCACGGCCCCGGCGTCCGCCTCCGTCCCC CGGCCTCCGCGAGCGCCGCGGAAGCCC______CGGCCACGGCCCCGGCGTCCGCCTCCGTCCCC CCGGCCA C CHRM5 Ensembl:ENSG00000184984 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34038727..34039181 26863196 MeRIP-seq:(Medium) rs1035895081 Functional Loss DEL dbSNP153 28..33 33 - - - 61627 RMVar_ID_61627 Human_SNP_ID_572872762 m1A Human chr15 + 34038882 34038882 34038882 CGGCCTCCGCGAGCGCCGCGGAAGCCCCGGCCACGGCCACGGCCCCGGCGTCCGCCTCCGTCCCC CGGCCTCCGCGAGCGCCGCGGAAGCCCCGGCCCCGGCCACGGCCCCGGCGTCCGCCTCCGTCCCC A C CHRM5 Ensembl:ENSG00000184984 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34038727..34039181 26863196 MeRIP-seq:(Medium) rs1199602571 Functional Loss SNV dbSNP153 33..33 33 - - - 61628 RMVar_ID_61628 Human_SNP_ID_572872774 m1A Human chr15 - 34038900 34038900 34038900 GGCGGCGGAGGCGGCGGCGGGGACGGAGGCGGACGCCGGGGCCGTGGCCGTGGCCGGGGCTTCCG GGCGGCGGAGGCGGCGGCGGGGACGGAGGCGGGCGCCGGGGCCGTGGCCGTGGCCGGGGCTTCCG T C AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:34038833..34038932 26863410 MeRIP-seq:(Medium) rs1215448226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232752 61629 RMVar_ID_61629 Human_SNP_ID_572872791 m1A Human chr15 - 34038924 34038912 34038924 GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGGAGGCGGCGGCGGGGACGGAGGCGGACGCCGGGG GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGG____________GGACGGAGGCGGACGCCGGGG CCCGCCGCCGCCT C AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:34038784..34039078 26863196 MeRIP-seq:(Medium) rs758764557 Functional Loss DEL dbSNP153,HGVD 33..44 33 - - - 61630 RMVar_ID_61630 Human_SNP_ID_572872796 m1A Human chr15 - 34038924 34038915 34038924 GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGGAGGCGGCGGCGGGGACGGAGGCGGACGCCGGGG GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGG_________CGGGGACGGAGGCGGACGCCGGGG GCCGCCGCCT G AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:34038784..34039078 26863196 MeRIP-seq:(Medium) rs910904456 Functional Loss DEL dbSNP153 33..41 33 - - - 61631 RMVar_ID_61631 Human_SNP_ID_572872804 m1A Human chr15 - 34038924 34038924 34038924 GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGGAGGCGGCGGCGGGGACGGAGGCGGACGCCGGGG GCCGCAGCGGCGGTAGCCAGAGGCGGCGGCGGGGGCGGCGGCGGGGACGGAGGCGGACGCCGGGG T C AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:34038784..34039078 26863196 MeRIP-seq:(Medium) rs1278945833 Functional Loss SNV dbSNP153 33..33 33 - - - 61632 RMVar_ID_61632 Human_SNP_ID_572883760 m1A Human chr15 - 34084320 34084320 34084320 GGCTGGCAAAAGGAGGTAGTCAGGCCGTCCAGAGCTGGCATTTGCACAAACACGGCAACACTGGG GGCTGGCAAAAGGAGGTAGTCAGGCCGTCCAGCGCTGGCATTTGCACAAACACGGCAACACTGGG T G EMC7 Ensembl:ENSG00000134153 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34084270..34084500 26863196 MeRIP-seq:(Medium) rs1224522380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43118,Human_RBP_ID_455949,Human_RBP_ID_6418102,Human_RBP_ID_17652095 RMVar_hsa_circ_170521,RMVar_hsa_circ_170522,RMVar_hsa_circ_170520 61633 RMVar_ID_61633 Human_SNP_ID_572919590 m1A Human chr15 + 34225177 34225177 34225177 CGAGGCCGGCGCTTCAAGTGGGCCATTGAGCTAAGCGGGCCTGGAGGAGGCAGCAGGTGAGGCAC CGAGGCCGGCGCTTCAAGTGGGCCATTGAGCTCAGCGGGCCTGGAGGAGGCAGCAGGTGAGGCAC A C EMC4 Ensembl:ENSG00000128463 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:34225126..34225200 32194978 MeRIP-seq:(Medium) rs1325833655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232547,Human_RBP_ID_456008,Human_RBP_ID_4342210,Human_RBP_ID_5316056,Human_RBP_ID_5354819,Human_RBP_ID_21887653,Human_RBP_ID_22440517,Human_RBP_ID_22496135 Human_Splice_Rec_1579933,Human_Splice_Rec_1579939,Human_Splice_Rec_1579947,Human_Splice_Rec_1579953,Human_Splice_Rec_1579955,Human_Splice_Rec_1579959,Human_Splice_Rec_1579965,Human_Splice_Rec_1579973,Human_Splice_Rec_1579977,Human_Splice_Rec_1579981,Human_Splice_Rec_1579985 61634 RMVar_ID_61634 Human_SNP_ID_572920218 m1A Human chr15 - 34227683 34227679 34227684 CCCAAGGCGATGTCCCAGCAGCGCTAAAACAAAACACACAATTTTAACCCTCTGATCACTACCCT CCCAAGGCGATGTCCCAGCAGCGCTAAAACA_____CACAATTTTAACCCTCTGATCACTACCCT GTGTTT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34227676..34227825 32194978 MeRIP-seq:(Medium) rs773413671 Functional Loss DEL dbSNP153 32..36 33 - - - 61635 RMVar_ID_61635 Human_SNP_ID_572920471 m1A Human chr15 - 34228553 34228553 34228553 GGGGGCTCAATGAAGGCTAACCAATCCGATGCATGTGTAGGTAACAGTCCCATGGACTGGCACTT GGGGGCTCAATGAAGGCTAACCAATCCGATGCGTGTGTAGGTAACAGTCCCATGGACTGGCACTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34228502..34228613 26863196 MeRIP-seq:(Medium) rs577317699 Functional Loss SNV dbSNP153 33..33 33 - - - 61636 RMVar_ID_61636 Human_SNP_ID_572941017 m1A Human chr15 + 34311748 34311748 34311748 ATTAATAACACTTCCATAAATGGCCTCAATCTACCTCTCTCCCTCATCTCTTATCTCTTTACCAC ATTAATAACACTTCCATAAATGGCCTCAATCTGCCTCTCTCCCTCATCTCTTATCTCTTTACCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:34311745..34311865 26863196 MeRIP-seq:(Medium) rs1173074958 Functional Loss SNV dbSNP153 33..33 33 - - - 61637 RMVar_ID_61637 Human_SNP_ID_572947587 m1A Human chr15 - 34337815 34337815 34337815 CGTCGGGCCGGGGAGGGGGCGCCAGCCCCGGCAGCGCGAACCCTGCGCGCGCCGCGGCTCTGAAA CGTCGGGCCGGGGAGGGGGCGCCAGCCCCGGCGGCGCGAACCCTGCGCGCGCCGCGGCTCTGAAA T C SLC12A6 Ensembl:ENSG00000140199 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:34337768..34337954 26863196 MeRIP-seq:(Medium) rs1275027475 Functional Loss SNV dbSNP153 33..33 33 - - - 61638 RMVar_ID_61638 Human_SNP_ID_572947622 m1A Human chr15 + 34337881 34337881 34337881 CAGAGCAGCAGTTACGTGACCTGGCCTCCCCCAGCCCCGGGCCCGACGGGGTGCGCCCGCGCCGC CAGAGCAGCAGTTACGTGACCTGGCCTCCCCCTGCCCCGGGCCCGACGGGGTGCGCCCGCGCCGC A T NONHSAG016487.2 RNACentral:URS00008BD6FB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34337752..34338010 26863196 MeRIP-seq:(Medium) rs549669648 Functional Loss SNV dbSNP153 33..33 33 - - - 61639 RMVar_ID_61639 Human_SNP_ID_572948751 m1A Human chr15 + 34341935 34341935 34341935 AGAGTTTGGTTACGGAGTCTCCGAGGGGTAACAGGTGGCAGAAAAGACATCAGTTTAAGGGACCC AGAGTTTGGTTACGGAGTCTCCGAGGGGTAACGGGTGGCAGAAAAGACATCAGTTTAAGGGACCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34341886..34342144 26863196 MeRIP-seq:(Medium) rs375648407 Functional Loss SNV dbSNP153 33..33 33 - - - 61640 RMVar_ID_61640 Human_SNP_ID_572948752 m1A Human chr15 + 34341935 34341935 34341935 AGAGTTTGGTTACGGAGTCTCCGAGGGGTAACAGGTGGCAGAAAAGACATCAGTTTAAGGGACCC AGAGTTTGGTTACGGAGTCTCCGAGGGGTAACTGGTGGCAGAAAAGACATCAGTTTAAGGGACCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34341886..34342144 26863196 MeRIP-seq:(Medium) rs375648407 Functional Loss SNV dbSNP153 33..33 33 - - - 61641 RMVar_ID_61641 Human_SNP_ID_572949129 m1A Human chr15 - 34343083 34343083 34343083 TGAGCGGTGGACCGAATTGGGACCGCTGGCTTATAAGCGATCATGTTTCTCCAGTATTACCTCAA TGAGCGGTGGACCGAATTGGGACCGCTGGCTTGTAAGCGATCATGTTTCTCCAGTATTACCTCAA T C NOP10 Ensembl:ENSG00000182117 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34341804..34343085 32194978 MeRIP-seq:(Medium) rs746040045 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_456050,Human_RBP_ID_1174276,Human_RBP_ID_1277936,Human_RBP_ID_1503860,Human_RBP_ID_4342543,Human_RBP_ID_5463953,Human_RBP_ID_23648580,Human_RBP_ID_24473227,Human_RBP_ID_27230882 Human_Splice_Rec_1580621,Human_Splice_Rec_1580623 Human_miRNA_ID_2731968 RMVar_hsa_circ_102468,RMVar_hsa_circ_170546 61642 RMVar_ID_61642 Human_SNP_ID_572949132 m1A Human chr15 + 34343089 34343089 34343089 TAATACTGGAGAAACATGATCGCTTATAAGCCAGCGGTCCCAATTCGGTCCACCGCTCAGTCTGC TAATACTGGAGAAACATGATCGCTTATAAGCCGGCGGTCCCAATTCGGTCCACCGCTCAGTCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:34342914..34343150;chr15:34342845..34343150 26863196 MeRIP-seq:(Medium) rs764894891 Functional Loss SNV dbSNP153 33..33 33 - - - 61643 RMVar_ID_61643 Human_SNP_ID_572949133 m1A Human chr15 + 34343089 34343089 34343089 TAATACTGGAGAAACATGATCGCTTATAAGCCAGCGGTCCCAATTCGGTCCACCGCTCAGTCTGC TAATACTGGAGAAACATGATCGCTTATAAGCCTGCGGTCCCAATTCGGTCCACCGCTCAGTCTGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:34342914..34343150;chr15:34342845..34343150 26863196 MeRIP-seq:(Medium) rs764894891 Functional Loss SNV dbSNP153 33..33 33 - - - 61644 RMVar_ID_61644 Human_SNP_ID_572949155 m1A Human chr15 - 34343117 34343117 34343117 AACACGTGACGCGGTCGGGCGGACCACTGCAGACTGAGCGGTGGACCGAATTGGGACCGCTGGCT AACACGTGACGCGGTCGGGCGGACCACTGCAGGCTGAGCGGTGGACCGAATTGGGACCGCTGGCT T C NOP10 Ensembl:ENSG00000182117 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:34343101..34343150 26863196 MeRIP-seq:(Medium) rs1379888710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456051,Human_RBP_ID_815290,Human_RBP_ID_4342213,Human_RBP_ID_17366857,Human_RBP_ID_17688330 Human_Splice_Rec_1580621,Human_Splice_Rec_1580623 RMVar_hsa_circ_102468,RMVar_hsa_circ_170546 61645 RMVar_ID_61645 Human_SNP_ID_572953763 m1A Human chr15 - 34359220 34359220 34359220 AGCACCTACCTGCGCCCCCCACACACCTCTCGAGGCACCTCCCAGACACCAAATGCCTCATCCCC AGCACCTACCTGCGCCCCCCACACACCTCTCGTGGCACCTCCCAGACACCAAATGCCTCATCCCC T A LPCAT4 Ensembl:ENSG00000176454 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34359051..34359275 26863196 MeRIP-seq:(Medium) rs1013442627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759725 Human_Splice_Rec_1580702,Human_Splice_Rec_1580710,Human_Splice_Rec_1580734,Human_Splice_Rec_1580742 61646 RMVar_ID_61646 Human_SNP_ID_572954560 m1A Human chr15 + 34362247 34362247 34362247 TTCCCAGTTCCCAGAGCTGTGGTTCCAACGCCACCTTCAGCCGGCCCACCACAATCACAGGTAAG TTCCCAGTTCCCAGAGCTGTGGTTCCAACGCCTCCTTCAGCCGGCCCACCACAATCACAGGTAAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34362148..34362274 26863196 MeRIP-seq:(Medium) rs1400289801 Functional Loss SNV dbSNP153 33..33 33 - - - 61647 RMVar_ID_61647 Human_SNP_ID_572955459 m1A Human chr15 + 34365091 34365091 34365091 GGTCACAGGGCAGCAGAACAATGGGGTCAAAGAAAGTGGAGTGTGGGGCAGCAACAAGGACAGGG GGTCACAGGGCAGCAGAACAATGGGGTCAAAGCAAGTGGAGTGTGGGGCAGCAACAAGGACAGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34364972..34365212 26863196 MeRIP-seq:(Medium) rs1201515182 Functional Loss SNV dbSNP153 33..33 33 - - - 61648 RMVar_ID_61648 Human_SNP_ID_572955919 m1A Human chr15 + 34366843 34366843 34366843 CCAGGACTCCTTGCCCAACCGCGGCCGCCCCCACGTGCGCACCCCCGGACTCCCGCTCCGCAAGC CCAGGACTCCTTGCCCAACCGCGGCCGCCCCCGCGTGCGCACCCCCGGACTCCCGCTCCGCAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34366660..34366969 26863196 MeRIP-seq:(Medium) rs994669391 Functional Loss SNV dbSNP153 33..33 33 - - - 61649 RMVar_ID_61649 Human_SNP_ID_572956048 m1A Human chr15 + 34367117 34367117 34367117 GACTTCCCTGGCTCATGGCGGGAGAAGGTGGGAGGGAGGGCACCCCGGCCCTGGCCCCGGCCACC GACTTCCCTGGCTCATGGCGGGAGAAGGTGGGGGGGAGGGCACCCCGGCCCTGGCCCCGGCCACC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:34367026..34367200 26863410 MeRIP-seq:(Medium) rs913372527 Functional Loss SNV dbSNP153 33..33 33 - - - 61650 RMVar_ID_61650 Human_SNP_ID_572956058 m1A Human chr15 - 34367136 34367136 34367136 AGCAGCTGCTCTGCAGAGTGGTGGCCGGGGCCAGGGCCGGGGTGCCCTCCCTCCCACCTTCTCCC AGCAGCTGCTCTGCAGAGTGGTGGCCGGGGCCGGGGCCGGGGTGCCCTCCCTCCCACCTTCTCCC T C LPCAT4 Ensembl:ENSG00000176454 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34367091..34367178 26863196 MeRIP-seq:(Medium) rs1265360272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456075,Human_RBP_ID_4342216,Human_RBP_ID_23127322 61651 RMVar_ID_61651 Human_SNP_ID_572961938 m1A Human chr15 + 34386862 34386862 34386862 GGGAGGAGGTTGGAGGGCTGGCCTGCGGGGTCACTGCACCTCCGCCCAGAGCCTCCTACCTCCAG GGGAGGAGGTTGGAGGGCTGGCCTGCGGGGTCCCTGCACCTCCGCCCAGAGCCTCCTACCTCCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:34386779..34386878 26863196 MeRIP-seq:(Medium) rs1386617742 Functional Loss SNV dbSNP153 33..33 33 - - - 61652 RMVar_ID_61652 Human_SNP_ID_572972147 m1A Human chr15 - 34435440 34435440 34435440 GGAATAATCGGTGGAGATGGATTGTGAAATGGAGGTGCATAAATATCCAGTTTGCCAACCGAGCT GGAATAATCGGTGGAGATGGATTGTGAAATGGGGGTGCATAAATATCCAGTTTGCCAACCGAGCT T C GOLGA8A Ensembl:ENSG00000175265 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:34435401..34435475 26863196 MeRIP-seq:(Medium) rs898915166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884132,Human_RBP_ID_2437849,Human_RBP_ID_5179324,Human_RBP_ID_5566247,Human_RBP_ID_9371416,Human_RBP_ID_17651908,Human_RBP_ID_18981328,Human_RBP_ID_22047380,Human_RBP_ID_22934637,Human_RBP_ID_26326459,Human_RBP_ID_27809291 Human_Splice_Rec_1580864,Human_Splice_Rec_1580865 RMVar_hsa_circ_268920 61653 RMVar_ID_61653 Human_SNP_ID_572973099 m1A Human chr15 - 34437689 34437689 34437689 AGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGACGGCGGCGCGGCGAG AGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGTCGGCGGCGCGGCGAGGACGGCGGCGCGGCGAG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:34437673..34437755 26863410 MeRIP-seq:(Medium) rs1217241200 Functional Loss SNV dbSNP153 33..33 33 - - - 61654 RMVar_ID_61654 Human_SNP_ID_572973100 m1A Human chr15 - 34437689 34437689 34437689 AGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGACGGCGGCGCGGCGAG AGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGGCGGCGGCGCGGCGAGGACGGCGGCGCGGCGAG T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:34437673..34437755 26863410 MeRIP-seq:(Medium) rs1217241200 Functional Loss SNV dbSNP153 33..33 33 - - - 61655 RMVar_ID_61655 Human_SNP_ID_572973139 m1A Human chr15 - 34437721 34437721 34437721 TGCGGGAGCTCAGCCCCCGGGAGAGACCCGGCAGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGA TGCGGGAGCTCAGCCCCCGGGAGAGACCCGGCGGCGGCGCGGCGAGGACGGCGGCGCGGCGAGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:34437376..34437800 26863196 MeRIP-seq:(Medium) rs774886108 Functional Loss SNV dbSNP153 33..33 33 - - - 61656 RMVar_ID_61656 Human_SNP_ID_572973145 m1A Human chr15 - 34437728 34437728 34437728 CGAGCTCTGCGGGAGCTCAGCCCCCGGGAGAGACCCGGCAGCGGCGCGGCGAGGACGGCGGCGCG CGAGCTCTGCGGGAGCTCAGCCCCCGGGAGAGGCCCGGCAGCGGCGCGGCGAGGACGGCGGCGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:34437683..34437769 26863410 MeRIP-seq:(Medium) rs1374925528 Functional Loss SNV dbSNP153 33..33 33 - - - 61657 RMVar_ID_61657 Human_SNP_ID_572973156 m1A Human chr15 - 34437747 34437747 34437747 CGAGGTGTGCGGCTAGGCGCGAGCTCTGCGGGAGCTCAGCCCCCGGGAGAGACCCGGCAGCGGCG CGAGGTGTGCGGCTAGGCGCGAGCTCTGCGGGTGCTCAGCCCCCGGGAGAGACCCGGCAGCGGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr15:34437651..34437850;chr15:34437610..34437802;chr15:34437676..34437850 26863196 MeRIP-seq:(Medium) rs1399380531 Functional Loss SNV dbSNP153 33..33 33 - - - 61658 RMVar_ID_61658 Human_SNP_ID_572983887 m1A Human chr15 + 34490459 34490459 34490459 ACCACATCGTCAATCAGGCCCCTGCTGTGGACAACTGGGGAGGCAGGGGTTTTGTGCAGGTCATG ACCACATCGTCAATCAGGCCCCTGCTGTGGACCACTGGGGAGGCAGGGGTTTTGTGCAGGTCATG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34490446..34490694 26863196 MeRIP-seq:(Medium) rs573298083 Functional Loss SNV dbSNP153 33..33 33 - - - 61659 RMVar_ID_61659 Human_SNP_ID_572995080 m1A Human chr15 - 34553952 34553952 34553952 CTTAAGCAACATCTATTTAATTTAACAGCTCTACTGAGATGAAGAAAGAAAAAGAATACCTGCTC CTTAAGCAACATCTATTTAATTTAACAGCTCTGCTGAGATGAAGAAAGAAAAAGAATACCTGCTC T C GOLGA8B Ensembl:ENSG00000215252 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:34553928..34554055 26863196 MeRIP-seq:(Medium) rs1397265534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885350,Human_RBP_ID_8230949,Human_RBP_ID_18418433,Human_RBP_ID_18982035 Human_Splice_Rec_1580932,Human_Splice_Rec_1580976,Human_Splice_Rec_1581054,Human_Splice_Rec_1581062,Human_Splice_Rec_1581068,Human_Splice_Rec_1581074 RMVar_hsa_circ_324496,RMVar_hsa_circ_6950 61660 RMVar_ID_61660 Human_SNP_ID_573052734 m1A Human chr15 + 34793555 34793555 34793555 TCATCACCTACGTAGGAGTCCTTCTGACCCATACCCACCATAACTCCCTATGAGAAGAAAAAATG TCATCACCTACGTAGGAGTCCTTCTGACCCATCCCCACCATAACTCCCTATGAGAAGAAAAAATG A C AC087457.1 Ensembl:ENSG00000250007 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34793505..34794766 32194978 MeRIP-seq:(Medium) rs770650598 Functional Loss SNV dbSNP153 33..33 33 - - - 61661 RMVar_ID_61661 Human_SNP_ID_573078315 m1A Human chr15 - 34904487 34904487 34904487 TTCAAATTGTCCAGGACCTGAACCCAGACCCAATCTTAGAGGAGAATCAAGGACATTTAGAGTGT TTCAAATTGTCCAGGACCTGAACCCAGACCCAGTCTTAGAGGAGAATCAAGGACATTTAGAGTGT T C AQR Ensembl:ENSG00000021776 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34904384..34906598 32194978 MeRIP-seq:(Medium) rs1310437647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888110,Human_RBP_ID_12490790 Human_Splice_Rec_1581188,Human_Splice_Rec_1581256 RMVar_hsa_circ_108498,RMVar_hsa_circ_78233,RMVar_hsa_circ_170555,RMVar_hsa_circ_78892,RMVar_hsa_circ_170558,RMVar_hsa_circ_114293,RMVar_hsa_circ_170561,RMVar_hsa_circ_84856,RMVar_hsa_circ_170562,RMVar_hsa_circ_170559,RMVar_hsa_circ_170560,RMVar_hsa_circ_37484,RMVar_hsa_circ_14096,RMVar_hsa_circ_22603,RMVar_hsa_circ_2164,RMVar_hsa_circ_2677,RMVar_hsa_circ_4028,RMVar_hsa_circ_39524,RMVar_hsa_circ_72643,RMVar_hsa_circ_117097,RMVar_hsa_circ_35893,RMVar_hsa_circ_80628,RMVar_hsa_circ_170567,RMVar_hsa_circ_121343,RMVar_hsa_circ_170568,RMVar_hsa_circ_368757,RMVar_hsa_circ_307777,RMVar_hsa_circ_89078,RMVar_hsa_circ_79367,RMVar_hsa_circ_23784,RMVar_hsa_circ_8730,RMVar_hsa_circ_170571,RMVar_hsa_circ_170572,RMVar_hsa_circ_170569,RMVar_hsa_circ_170570,RMVar_hsa_circ_170577,RMVar_hsa_circ_36603,RMVar_hsa_circ_170578,RMVar_hsa_circ_113132,RMVar_hsa_circ_315239,RMVar_hsa_circ_170579,RMVar_hsa_circ_328360,RMVar_hsa_circ_30848,RMVar_hsa_circ_21505,RMVar_hsa_circ_31574,RMVar_hsa_circ_170581,RMVar_hsa_circ_8649,RMVar_hsa_circ_9712,RMVar_hsa_circ_368235,RMVar_hsa_circ_170580,RMVar_hsa_circ_268147,RMVar_hsa_circ_60365,RMVar_hsa_circ_267427,RMVar_hsa_circ_377691,RMVar_hsa_circ_115011,RMVar_hsa_circ_293486,RMVar_hsa_circ_170586,RMVar_hsa_circ_372596,RMVar_hsa_circ_373182,RMVar_hsa_circ_371808,RMVar_hsa_circ_318789,RMVar_hsa_circ_117779,RMVar_hsa_circ_121392,RMVar_hsa_circ_84278,RMVar_hsa_circ_170587,RMVar_hsa_circ_170591,RMVar_hsa_circ_170593,RMVar_hsa_circ_26436,RMVar_hsa_circ_170594,RMVar_hsa_circ_170592,RMVar_hsa_circ_170589,RMVar_hsa_circ_170590,RMVar_hsa_circ_170588,RMVar_hsa_circ_32035,RMVar_hsa_circ_106178,RMVar_hsa_circ_170595 61662 RMVar_ID_61662 Human_SNP_ID_573078827 m1A Human chr15 - 34906589 34906589 34906589 GCAGGTTGGCCTGGTTTATGTCAGAGGCTGTGAAATTCAGGGCATGCTGGATGATAAAGGACGTG GCAGGTTGGCCTGGTTTATGTCAGAGGCTGTGGAATTCAGGGCATGCTGGATGATAAAGGACGTG T C AQR Ensembl:ENSG00000021776 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:34906511..34906595 26863196 MeRIP-seq:(Medium) rs75634603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3945336,Human_RBP_ID_8803767,Human_RBP_ID_9283573,Human_RBP_ID_23648750 Human_Splice_Rec_1581187,Human_Splice_Rec_1581255 Human_miRNA_ID_707330,Human_miRNA_ID_714582,Human_miRNA_ID_969989,Human_miRNA_ID_1516376,Human_miRNA_ID_2441839,Human_miRNA_ID_2452567,Human_miRNA_ID_2898950,Human_miRNA_ID_3090827 RMVar_hsa_circ_108498,RMVar_hsa_circ_78233,RMVar_hsa_circ_170555,RMVar_hsa_circ_78892,RMVar_hsa_circ_170558,RMVar_hsa_circ_114293,RMVar_hsa_circ_170561,RMVar_hsa_circ_84856,RMVar_hsa_circ_170559,RMVar_hsa_circ_170560,RMVar_hsa_circ_37484,RMVar_hsa_circ_14096,RMVar_hsa_circ_22603,RMVar_hsa_circ_2164,RMVar_hsa_circ_39524,RMVar_hsa_circ_72643,RMVar_hsa_circ_117097,RMVar_hsa_circ_35893,RMVar_hsa_circ_80628,RMVar_hsa_circ_170567,RMVar_hsa_circ_121343,RMVar_hsa_circ_170568,RMVar_hsa_circ_368757,RMVar_hsa_circ_89078,RMVar_hsa_circ_79367,RMVar_hsa_circ_23784,RMVar_hsa_circ_8730,RMVar_hsa_circ_170571,RMVar_hsa_circ_170569,RMVar_hsa_circ_170570,RMVar_hsa_circ_36603,RMVar_hsa_circ_170578,RMVar_hsa_circ_113132,RMVar_hsa_circ_170579,RMVar_hsa_circ_328360,RMVar_hsa_circ_30848,RMVar_hsa_circ_21505,RMVar_hsa_circ_31574,RMVar_hsa_circ_8649,RMVar_hsa_circ_9712,RMVar_hsa_circ_368235,RMVar_hsa_circ_170580,RMVar_hsa_circ_268147,RMVar_hsa_circ_60365,RMVar_hsa_circ_267427,RMVar_hsa_circ_377691,RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_372596,RMVar_hsa_circ_373182,RMVar_hsa_circ_371808,RMVar_hsa_circ_318789,RMVar_hsa_circ_117779,RMVar_hsa_circ_121392,RMVar_hsa_circ_84278,RMVar_hsa_circ_170587,RMVar_hsa_circ_170591,RMVar_hsa_circ_170593,RMVar_hsa_circ_26436,RMVar_hsa_circ_170592,RMVar_hsa_circ_170589,RMVar_hsa_circ_170590,RMVar_hsa_circ_170588,RMVar_hsa_circ_87507,RMVar_hsa_circ_106178,RMVar_hsa_circ_170595,RMVar_hsa_circ_325131,RMVar_hsa_circ_170596,RMVar_hsa_circ_170597 61663 RMVar_ID_61663 Human_SNP_ID_573079618 m1A Human chr15 - 34910219 34910219 34910219 CTTTCACTGTCGTTGAAGTGGCCAAACCCAACATAGGTGAAAACTGGCCAACCCGAGTTCGTGCA CTTTCACTGTCGTTGAAGTGGCCAAACCCAACGTAGGTGAAAACTGGCCAACCCGAGTTCGTGCA T C AQR Ensembl:ENSG00000021776 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34910169..34910269 32194978 MeRIP-seq:(Medium) rs749357429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8230854,Human_RBP_ID_9283574,Human_RBP_ID_23648752 Human_Splice_Rec_1581184,Human_Splice_Rec_1581185,Human_Splice_Rec_1581252,Human_Splice_Rec_1581253 RMVar_hsa_circ_108498,RMVar_hsa_circ_78233,RMVar_hsa_circ_170555,RMVar_hsa_circ_78892,RMVar_hsa_circ_170558,RMVar_hsa_circ_114293,RMVar_hsa_circ_170561,RMVar_hsa_circ_84856,RMVar_hsa_circ_170559,RMVar_hsa_circ_170560,RMVar_hsa_circ_37484,RMVar_hsa_circ_14096,RMVar_hsa_circ_5522,RMVar_hsa_circ_22603,RMVar_hsa_circ_2164,RMVar_hsa_circ_39524,RMVar_hsa_circ_72643,RMVar_hsa_circ_117097,RMVar_hsa_circ_35893,RMVar_hsa_circ_80628,RMVar_hsa_circ_170567,RMVar_hsa_circ_121343,RMVar_hsa_circ_170568,RMVar_hsa_circ_368757,RMVar_hsa_circ_89078,RMVar_hsa_circ_79367,RMVar_hsa_circ_23784,RMVar_hsa_circ_8730,RMVar_hsa_circ_170571,RMVar_hsa_circ_170569,RMVar_hsa_circ_170570,RMVar_hsa_circ_36603,RMVar_hsa_circ_170578,RMVar_hsa_circ_113132,RMVar_hsa_circ_170579,RMVar_hsa_circ_328360,RMVar_hsa_circ_30848,RMVar_hsa_circ_21505,RMVar_hsa_circ_31574,RMVar_hsa_circ_8649,RMVar_hsa_circ_9712,RMVar_hsa_circ_368235,RMVar_hsa_circ_170580,RMVar_hsa_circ_268147,RMVar_hsa_circ_60365,RMVar_hsa_circ_267427,RMVar_hsa_circ_377691,RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_372596,RMVar_hsa_circ_373182,RMVar_hsa_circ_371808,RMVar_hsa_circ_318789,RMVar_hsa_circ_121392,RMVar_hsa_circ_84278,RMVar_hsa_circ_170587,RMVar_hsa_circ_170591,RMVar_hsa_circ_26436,RMVar_hsa_circ_170592,RMVar_hsa_circ_170589,RMVar_hsa_circ_170590,RMVar_hsa_circ_170588,RMVar_hsa_circ_106178,RMVar_hsa_circ_170595,RMVar_hsa_circ_325131,RMVar_hsa_circ_50390,RMVar_hsa_circ_170597,RMVar_hsa_circ_355718,RMVar_hsa_circ_378416,RMVar_hsa_circ_47062 61664 RMVar_ID_61664 Human_SNP_ID_573079619 m1A Human chr15 - 34910219 34910219 34910219 CTTTCACTGTCGTTGAAGTGGCCAAACCCAACATAGGTGAAAACTGGCCAACCCGAGTTCGTGCA CTTTCACTGTCGTTGAAGTGGCCAAACCCAACCTAGGTGAAAACTGGCCAACCCGAGTTCGTGCA T G AQR Ensembl:ENSG00000021776 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34910169..34910269 32194978 MeRIP-seq:(Medium) rs749357429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8230854,Human_RBP_ID_9283574,Human_RBP_ID_23648752 Human_Splice_Rec_1581184,Human_Splice_Rec_1581185,Human_Splice_Rec_1581252,Human_Splice_Rec_1581253 RMVar_hsa_circ_108498,RMVar_hsa_circ_78233,RMVar_hsa_circ_170555,RMVar_hsa_circ_78892,RMVar_hsa_circ_170558,RMVar_hsa_circ_114293,RMVar_hsa_circ_170561,RMVar_hsa_circ_84856,RMVar_hsa_circ_170559,RMVar_hsa_circ_170560,RMVar_hsa_circ_37484,RMVar_hsa_circ_14096,RMVar_hsa_circ_5522,RMVar_hsa_circ_22603,RMVar_hsa_circ_2164,RMVar_hsa_circ_39524,RMVar_hsa_circ_72643,RMVar_hsa_circ_117097,RMVar_hsa_circ_35893,RMVar_hsa_circ_80628,RMVar_hsa_circ_170567,RMVar_hsa_circ_121343,RMVar_hsa_circ_170568,RMVar_hsa_circ_368757,RMVar_hsa_circ_89078,RMVar_hsa_circ_79367,RMVar_hsa_circ_23784,RMVar_hsa_circ_8730,RMVar_hsa_circ_170571,RMVar_hsa_circ_170569,RMVar_hsa_circ_170570,RMVar_hsa_circ_36603,RMVar_hsa_circ_170578,RMVar_hsa_circ_113132,RMVar_hsa_circ_170579,RMVar_hsa_circ_328360,RMVar_hsa_circ_30848,RMVar_hsa_circ_21505,RMVar_hsa_circ_31574,RMVar_hsa_circ_8649,RMVar_hsa_circ_9712,RMVar_hsa_circ_368235,RMVar_hsa_circ_170580,RMVar_hsa_circ_268147,RMVar_hsa_circ_60365,RMVar_hsa_circ_267427,RMVar_hsa_circ_377691,RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_372596,RMVar_hsa_circ_373182,RMVar_hsa_circ_371808,RMVar_hsa_circ_318789,RMVar_hsa_circ_121392,RMVar_hsa_circ_84278,RMVar_hsa_circ_170587,RMVar_hsa_circ_170591,RMVar_hsa_circ_26436,RMVar_hsa_circ_170592,RMVar_hsa_circ_170589,RMVar_hsa_circ_170590,RMVar_hsa_circ_170588,RMVar_hsa_circ_106178,RMVar_hsa_circ_170595,RMVar_hsa_circ_325131,RMVar_hsa_circ_50390,RMVar_hsa_circ_170597,RMVar_hsa_circ_355718,RMVar_hsa_circ_378416,RMVar_hsa_circ_47062 61665 RMVar_ID_61665 Human_SNP_ID_573094763 m1A Human chr15 - 34969639 34969639 34969639 TTGCCGCTGCCCAGAGCGGTCCTTTAGTTTCCACTGGAGTGGAGGGAAGAGTGCTGCCATGGCAG TTGCCGCTGCCCAGAGCGGTCCTTTAGTTTCCGCTGGAGTGGAGGGAAGAGTGCTGCCATGGCAG T C AQR Ensembl:ENSG00000021776 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34969588..34969689 32194978 MeRIP-seq:(Medium) rs759283394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41117,Human_RBP_ID_4318338,Human_RBP_ID_8803771,Human_RBP_ID_9283576,Human_RBP_ID_9370668,Human_RBP_ID_18661592,Human_RBP_ID_22934639,Human_RBP_ID_26327979 RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_82898,RMVar_hsa_circ_170616 61666 RMVar_ID_61666 Human_SNP_ID_573158751 m1A Human chr15 + 35237930 35237928 35237931 GGAGGAAGGTGAAGAGGAGGACGTGAGTGGAGAGGAGGAGGAGGATGAAAAAGGTTATAACGATG GGAGGAAGGTGAAGAGGAGGACGTGAGTGGA___GAGGAGGAGGATGAAAAAGGTTATAACGATG AGAG A ANP32AP1 Ensembl:ENSG00000259516 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:35237815..35237965 26863196 MeRIP-seq:(Medium) rs560600149 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1130476,Human_RBP_ID_2438186,Human_RBP_ID_4344368,Human_RBP_ID_5095794,Human_RBP_ID_6419233,Human_RBP_ID_8251351,Human_RBP_ID_8804303,Human_RBP_ID_18512837 61667 RMVar_ID_61667 Human_SNP_ID_573232007 m1A Human chr15 + 35546134 35546134 35546134 CTCCAGGACCGCATTACCTGATCAGAGCCGCGACCCTCATGCTGGGCGCAGTGCGCGTGCGTGCG CTCCAGGACCGCATTACCTGATCAGAGCCGCGCCCCTCATGCTGGGCGCAGTGCGCGTGCGTGCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:35546050..35546136 26863196 MeRIP-seq:(Medium) rs780683833 Functional Loss SNV dbSNP153 33..33 33 - - - 61668 RMVar_ID_61668 Human_SNP_ID_573572799 m1A Human chr15 + 37002326 37002326 37002326 CCTCCTCCCCGCTTCTGCAGCCTCCTTAAAACATCTACTAATTTCTTCAGCTGGAAGTAATCTTT CCTCCTCCCCGCTTCTGCAGCCTCCTTAAAACGTCTACTAATTTCTTCAGCTGGAAGTAATCTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:37002309..37002375 26863196 MeRIP-seq:(Medium) rs1249584268 Functional Loss SNV dbSNP153 33..33 33 - - - 61669 RMVar_ID_61669 Human_SNP_ID_573595483 m1A Human chr15 - 37100483 37100483 37100483 GCTCCTCCTCGCTCCCGCTCCCCACTCCCGGGATGTGTCTCCGCCGTACGACGGGCTATGGCCAC GCTCCTCCTCGCTCCCGCTCCCCACTCCCGGGTTGTGTCTCCGCCGTACGACGGGCTATGGCCAC T A MEIS2 Ensembl:ENSG00000134138 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:37100437..37100511 26863196 MeRIP-seq:(Medium) rs1188327310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4318605 61670 RMVar_ID_61670 Human_SNP_ID_573595811 m1A Human chr15 + 37101271 37101271 37101271 GCCGCGGCGGAATCGGGAGGGAGGAAGTGAGGAGGCAGTCATCTGGGTCCGATGTAGCCAAAGGC GCCGCGGCGGAATCGGGAGGGAGGAAGTGAGGGGGCAGTCATCTGGGTCCGATGTAGCCAAAGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:37100896..37101320 26863196 MeRIP-seq:(Medium) rs1183968637 Functional Loss SNV dbSNP153 33..33 33 - - - 61671 RMVar_ID_61671 Human_SNP_ID_573596050 m1A Human chr15 + 37101597 37101597 37101597 TTACACAGGGGCGATTTCGCGGGGTCAGGGAGATGGGGCCAGCTCCGAAAGAACTTTTCCAAAAA TTACACAGGGGCGATTTCGCGGGGTCAGGGAGTTGGGGCCAGCTCCGAAAGAACTTTTCCAAAAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:37101492..37101599 26863196 MeRIP-seq:(Medium) rs556810271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25134945 61672 RMVar_ID_61672 Human_SNP_ID_573931974 m1A Human chr15 + 38454188 38454188 38454188 AGGACCATGAGAGGGCCGGAGCCGGGTCCCCAACCGACGATGGAGGGAGACGTGCTGGACACACT AGGACCATGAGAGGGCCGGAGCCGGGTCCCCAGCCGACGATGGAGGGAGACGTGCTGGACACACT A G FAM98B Ensembl:ENSG00000171262 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:38454126..38454289 26863196 MeRIP-seq:(Medium) rs201086439 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_456325,Human_RBP_ID_4318686,Human_RBP_ID_6421050 Human_Splice_Rec_1582357,Human_Splice_Rec_1582371 61673 RMVar_ID_61673 Human_SNP_ID_573931977 m1A Human chr15 + 38454195 38454195 38454195 TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGATGGAGGGAGACGTGCTGGACACACTGGAGGCG TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGGTGGAGGGAGACGTGCTGGACACACTGGAGGCG A G FAM98B Ensembl:ENSG00000171262 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:38454144..38464108 26863196 MeRIP-seq:(Medium) rs750510877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456325,Human_RBP_ID_4318686,Human_RBP_ID_6421050,Human_RBP_ID_18661780 Human_Splice_Rec_1582357,Human_Splice_Rec_1582371 61674 RMVar_ID_61674 Human_SNP_ID_573931978 m1A Human chr15 + 38454195 38454195 38454195 TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGATGGAGGGAGACGTGCTGGACACACTGGAGGCG TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGTTGGAGGGAGACGTGCTGGACACACTGGAGGCG A T FAM98B Ensembl:ENSG00000171262 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:38454144..38464108 26863196 MeRIP-seq:(Medium) rs750510877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456325,Human_RBP_ID_4318686,Human_RBP_ID_6421050,Human_RBP_ID_18661780 Human_Splice_Rec_1582357,Human_Splice_Rec_1582371 61675 RMVar_ID_61675 Human_SNP_ID_573932970 m1A Human chr15 + 38458136 38458136 38458136 AACCTTGGGGAGACACAGAAAGGGCCCATGCCAGGCACTTAGCTAGAGGCAAGCGTAGCTTTTGG AACCTTGGGGAGACACAGAAAGGGCCCATGCCGGGCACTTAGCTAGAGGCAAGCGTAGCTTTTGG A G FAM98B Ensembl:ENSG00000171262 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:38458135..38458235 32194978 MeRIP-seq:(Medium) rs552139893 Functional Loss SNV dbSNP153 33..33 33 - - - 61676 RMVar_ID_61676 Human_SNP_ID_573934386 m1A Human chr15 - 38463983 38463983 38463983 ACAAGTTAAAAACTAAATAAGCCAATCAAACAAAAAAACCTCCAACACTCTGTGTCAAGGTCTGC ACAAGTTAAAAACTAAATAAGCCAATCAAACAGAAAAACCTCCAACACTCTGTGTCAAGGTCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:38463980..38464125 26863196 MeRIP-seq:(Medium) rs1164156292 Functional Loss SNV dbSNP153 33..33 33 - - - 61677 RMVar_ID_61677 Human_SNP_ID_573938529 m1A Human chr15 + 38481451 38481451 38481451 GTGGCACCAGCCGGGAGAAGACCGCATGTGCCATTAATAAGGTTGGTGTTTCTTTCAGTACAGTG GTGGCACCAGCCGGGAGAAGACCGCATGTGCCGTTAATAAGGTTGGTGTTTCTTTCAGTACAGTG A G FAM98B Ensembl:ENSG00000171262 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:38481301..38481512;chr15:38474270..38481518 26863196 MeRIP-seq:(Medium) rs1306433344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1582369 RMVar_hsa_circ_170671,RMVar_hsa_circ_281124,RMVar_hsa_circ_296388 61678 RMVar_ID_61678 Human_SNP_ID_573939412 m1A Human chr15 - 38484506 38484506 38484506 CCATAATCTCCCCTGCCTTGGAAACCTCCTCTACCACCTCCTCCTCCTCCCCCCCACCCTCCTCC CCATAATCTCCCCTGCCTTGGAAACCTCCTCTTCCACCTCCTCCTCCTCCCCCCCACCCTCCTCC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:38484459..38484550 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 61679 RMVar_ID_61679 Human_SNP_ID_573939413 m1A Human chr15 - 38484506 38484506 38484506 CCATAATCTCCCCTGCCTTGGAAACCTCCTCTACCACCTCCTCCTCCTCCCCCCCACCCTCCTCC CCATAATCTCCCCTGCCTTGGAAACCTCCTCTGCCACCTCCTCCTCCTCCCCCCCACCCTCCTCC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:38484459..38484550 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 61680 RMVar_ID_61680 Human_SNP_ID_573957970 m1A Human chr15 + 38564698 38564698 38564698 GCGGCCGGGCGCGGCGCATCGCCCCCGCCACCACCGCCGCCGCCTGCCGGCTCTCTCCCCCCCGG GCGGCCGGGCGCGGCGCATCGCCCCCGCCACCCCCGCCGCCGCCTGCCGGCTCTCTCCCCCCCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:38564647..38564791 26863196 MeRIP-seq:(Medium) rs1038864342 Functional Loss SNV dbSNP153 33..33 33 - - - 61681 RMVar_ID_61681 Human_SNP_ID_574219292 m1A Human chr15 - 39581139 39581139 39581139 GGGCGCGGGGAATGCCTGTGCGTCCGGAGTAGAGGTTGCTCCTGGAGAGCGACAGGAGCCCTGAA GGGCGCGGGGAATGCCTGTGCGTCCGGAGTAGGGGTTGCTCCTGGAGAGCGACAGGAGCCCTGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:39581076..39581268 26863196 MeRIP-seq:(Medium) rs1475028029 Functional Loss SNV dbSNP153 33..33 33 - - - 61682 RMVar_ID_61682 Human_SNP_ID_574219297 m1A Human chr15 - 39581161 39581161 39581161 GCGAGGGCGGCGAGGGCTGGAGGGGCGCGGGGAATGCCTGTGCGTCCGGAGTAGAGGTTGCTCCT GCGAGGGCGGCGAGGGCTGGAGGGGCGCGGGGTATGCCTGTGCGTCCGGAGTAGAGGTTGCTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:39581113..39581244;chr15:39581111..39581269 26863196 MeRIP-seq:(Medium) rs1421426059 Functional Loss SNV dbSNP153 33..33 33 - - - 61683 RMVar_ID_61683 Human_SNP_ID_574219664 m1A Human chr15 - 39582300 39582300 39582300 AGGGGGGATCAGGTTGGCATCCTCGATGCGGAAAGCTGGGCTGGAAGGGTCGGGGCCCTTCACCA AGGGGGGATCAGGTTGGCATCCTCGATGCGGACAGCTGGGCTGGAAGGGTCGGGGCCCTTCACCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:39582253..39582663 26863196 MeRIP-seq:(Medium) rs1415248431 Functional Loss SNV dbSNP153 33..33 33 - - - 61684 RMVar_ID_61684 Human_SNP_ID_574222449 m1A Human chr15 + 39592671 39592671 39592671 GAACAATCTGGACAACTGTCCCTATGTGCCCAATGCCAACCAGGCTGACCATGACAAAGATGGCA GAACAATCTGGACAACTGTCCCTATGTGCCCAGTGCCAACCAGGCTGACCATGACAAAGATGGCA A G THBS1 Ensembl:ENSG00000137801 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:39592620..39592741 26863196 MeRIP-seq:(Medium) rs138397964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758900,Human_RBP_ID_815112,Human_RBP_ID_9370673,Human_RBP_ID_22387845 RMVar_hsa_circ_77636,RMVar_hsa_circ_103346,RMVar_hsa_circ_170691,RMVar_hsa_circ_77789,RMVar_hsa_circ_170692,RMVar_hsa_circ_103181,RMVar_hsa_circ_170699,RMVar_hsa_circ_127202,RMVar_hsa_circ_103875,RMVar_hsa_circ_118508,RMVar_hsa_circ_170707,RMVar_hsa_circ_170706,RMVar_hsa_circ_124452,RMVar_hsa_circ_91610,RMVar_hsa_circ_96287,RMVar_hsa_circ_88672,RMVar_hsa_circ_170717,RMVar_hsa_circ_170719,RMVar_hsa_circ_170720,RMVar_hsa_circ_170718,RMVar_hsa_circ_170716,RMVar_hsa_circ_118752,RMVar_hsa_circ_78254,RMVar_hsa_circ_170731,RMVar_hsa_circ_170732,RMVar_hsa_circ_121626,RMVar_hsa_circ_98455,RMVar_hsa_circ_114575,RMVar_hsa_circ_170740,RMVar_hsa_circ_99315,RMVar_hsa_circ_123527,RMVar_hsa_circ_170742,RMVar_hsa_circ_170743,RMVar_hsa_circ_170741,RMVar_hsa_circ_114314,RMVar_hsa_circ_76814,RMVar_hsa_circ_170764,RMVar_hsa_circ_170751,RMVar_hsa_circ_170753,RMVar_hsa_circ_170752,RMVar_hsa_circ_126317,RMVar_hsa_circ_90254,RMVar_hsa_circ_79988,RMVar_hsa_circ_170755,RMVar_hsa_circ_170756,RMVar_hsa_circ_170754,RMVar_hsa_circ_97392,RMVar_hsa_circ_107569,RMVar_hsa_circ_170762,RMVar_hsa_circ_170763,RMVar_hsa_circ_98597,RMVar_hsa_circ_115014,RMVar_hsa_circ_94028,RMVar_hsa_circ_170766,RMVar_hsa_circ_170765,RMVar_hsa_circ_77504,RMVar_hsa_circ_374388,RMVar_hsa_circ_106794,RMVar_hsa_circ_83310,RMVar_hsa_circ_170773,RMVar_hsa_circ_170775,RMVar_hsa_circ_170774,RMVar_hsa_circ_170772,RMVar_hsa_circ_83088,RMVar_hsa_circ_112067,RMVar_hsa_circ_76229,RMVar_hsa_circ_107145,RMVar_hsa_circ_170782,RMVar_hsa_circ_170783,RMVar_hsa_circ_170784,RMVar_hsa_circ_371511,RMVar_hsa_circ_373727,RMVar_hsa_circ_170786,RMVar_hsa_circ_170788,RMVar_hsa_circ_170787,RMVar_hsa_circ_110934,RMVar_hsa_circ_371575,RMVar_hsa_circ_372645,RMVar_hsa_circ_87872,RMVar_hsa_circ_170797,RMVar_hsa_circ_81389,RMVar_hsa_circ_170793,RMVar_hsa_circ_170795,RMVar_hsa_circ_170796,RMVar_hsa_circ_170794,RMVar_hsa_circ_170792,RMVar_hsa_circ_314597,RMVar_hsa_circ_372089,RMVar_hsa_circ_372229,RMVar_hsa_circ_170799,RMVar_hsa_circ_170800,RMVar_hsa_circ_170798,RMVar_hsa_circ_170804,RMVar_hsa_circ_100688,RMVar_hsa_circ_326129,RMVar_hsa_circ_374829,RMVar_hsa_circ_374892,RMVar_hsa_circ_124235,RMVar_hsa_circ_170806,RMVar_hsa_circ_98625,RMVar_hsa_circ_170807,RMVar_hsa_circ_170805,RMVar_hsa_circ_170802,RMVar_hsa_circ_170803 61685 RMVar_ID_61685 Human_SNP_ID_574314646 m1A Human chr15 + 39990946 39990946 39990946 GGGTAAGCAGACTTGGCTGTCGGAAGACCAGCATACTGTCTGACTGGTCGAAACTGTGAGGTGCA GGGTAAGCAGACTTGGCTGTCGGAAGACCAGCGTACTGTCTGACTGGTCGAAACTGTGAGGTGCA A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:39990940..39991060 26863196 MeRIP-seq:(Medium) rs956378792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89240,RMVar_hsa_circ_170841,RMVar_hsa_circ_23340,RMVar_hsa_circ_268465,RMVar_hsa_circ_13126,RMVar_hsa_circ_337510,RMVar_hsa_circ_339814,RMVar_hsa_circ_57910,RMVar_hsa_circ_347491 61686 RMVar_ID_61686 Human_SNP_ID_574315296 m1A Human chr15 + 39993471 39993471 39993471 AGGGAAGATCTCTTGAGAGGATGGCATTTAGGATAAAGGATGAGAAAGGACAAGCCACACAGATT AGGGAAGATCTCTTGAGAGGATGGCATTTAGGGTAAAGGATGAGAAAGGACAAGCCACACAGATT A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:39993421..39993648 26863196 MeRIP-seq:(Medium) rs974046812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12495083 RMVar_hsa_circ_89240,RMVar_hsa_circ_170841,RMVar_hsa_circ_268465,RMVar_hsa_circ_13126,RMVar_hsa_circ_347491 61687 RMVar_ID_61687 Human_SNP_ID_574325486 m1A Human chr15 + 40035488 40035488 40035488 AGACCCTGTCTTAAAAAAAAAAAGAAAAAAAAAATTTTTTTCTAAGAAGCTGTCCTACAAAGTTG AGACCCTGTCTTAAAAAAAAAAAGAAAAAAAATATTTTTTTCTAAGAAGCTGTCCTACAAAGTTG A T EIF2AK4 Ensembl:ENSG00000128829 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs897754817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4318945 RMVar_hsa_circ_119966,RMVar_hsa_circ_170858 61688 RMVar_ID_61688 Human_SNP_ID_574325694 m1A Human chr15 - 40036345 40036345 40036345 GCACCAACAACAGCAGCAACAACAGCAGCAACAGCAGCACAGTAAAGGGCATACATTTCCTGCTT GCACCAACAACAGCAGCAACAACAGCAGCAACGGCAGCACAGTAAAGGGCATACATTTCCTGCTT T C SRP14 Ensembl:ENSG00000140319 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40036294..40036514 26863196 MeRIP-seq:(Medium) rs1417559535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8415678,Human_RBP_ID_17249651,Human_RBP_ID_17364960,Human_RBP_ID_17481711,Human_RBP_ID_22190690 61689 RMVar_ID_61689 Human_SNP_ID_574325745 m1A Human chr15 - 40036375 40036375 40036375 GCAGCAGCAGCACCTGCCGCAGCAGCAACAGCACCAACAACAGCAGCAACAACAGCAGCAACAGC GCAGCAGCAGCACCTGCCGCAGCAGCAACAGCGCCAACAACAGCAGCAACAACAGCAGCAACAGC T C SRP14 Ensembl:ENSG00000140319 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:40036326..40036525;chr15:40036326..40036708 26863196 MeRIP-seq:(Medium) rs376432051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43182,Human_RBP_ID_17251768,Human_RBP_ID_26327307 61690 RMVar_ID_61690 Human_SNP_ID_574326514 m1A Human chr15 + 40038393 40038393 40038393 CCCTTCTTTGGAATGGGTTTGGTTCGACCGTCATCTGAAGGAAAAAATGCATCCTGGTGAACACG CCCTTCTTTGGAATGGGTTTGGTTCGACCGTCGTCTGAAGGAAAAAATGCATCCTGGTGAACACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:40038229..40038447;chr15:40038318..40038429;chr15:40038351..40038400;chr15:40038351..40038454 26863196 MeRIP-seq:(Medium) rs765631161 Functional Loss SNV dbSNP153 33..33 33 - - - 61691 RMVar_ID_61691 Human_SNP_ID_574326725 m1A Human chr15 + 40039033 40039033 40039033 CGCGTCAAGGCCCTGGTCCTCCTGCAGGAGGCACAGGTCTCGAGTAACGCCTGAGCCGCCCCCTT CGCGTCAAGGCCCTGGTCCTCCTGCAGGAGGCGCAGGTCTCGAGTAACGCCTGAGCCGCCCCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40039029..40039175 26863196 MeRIP-seq:(Medium) rs1057008746 Functional Loss SNV dbSNP153 33..33 33 - - - 61692 RMVar_ID_61692 Human_SNP_ID_574329514 m1A Human chr15 + 40050588 40050583 40050589 GGTGTGTGTGAGGAGTGTGTGGTGTGTGGGGGATTGTGGTGTGCGGGGGCGGTGGTGTGTGTGGT GGTGTGTGTGAGGAGTGTGTGGTGTGTG______TGTGGTGTGCGGGGGCGGTGGTGTGTGTGGT GGGGGAT G SRP14-AS1 Ensembl:ENSG00000248508 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40050580..40050667 26863196 MeRIP-seq:(Medium) rs1567018648 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_3489575,Human_RBP_ID_5236234,Human_RBP_ID_5287400,Human_RBP_ID_5646202,Human_RBP_ID_8081961,Human_RBP_ID_8182540,Human_RBP_ID_8230775,Human_RBP_ID_17252137,Human_RBP_ID_21969893 61693 RMVar_ID_61693 Human_SNP_ID_574329515 m1A Human chr15 + 40050588 40050588 40050588 GGTGTGTGTGAGGAGTGTGTGGTGTGTGGGGGATTGTGGTGTGCGGGGGCGGTGGTGTGTGTGGT GGTGTGTGTGAGGAGTGTGTGGTGTGTGGGGGGTTGTGGTGTGCGGGGGCGGTGGTGTGTGTGGT A G SRP14-AS1 Ensembl:ENSG00000248508 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40050580..40050667 26863196 MeRIP-seq:(Medium) rs929617952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489575,Human_RBP_ID_5236234,Human_RBP_ID_5287400,Human_RBP_ID_5646202,Human_RBP_ID_8081961,Human_RBP_ID_8182540,Human_RBP_ID_8230775,Human_RBP_ID_17252137,Human_RBP_ID_21969893 61694 RMVar_ID_61694 Human_SNP_ID_574331989 m1A Human chr15 + 40060749 40060749 40060749 AAAGAGCTGCCATCCGGGTAGGAGGAAGCCAGACCAGTGTGGAGTCCTGGACTCCAAAGAAAGAC AAAGAGCTGCCATCCGGGTAGGAGGAAGCCAGGCCAGTGTGGAGTCCTGGACTCCAAAGAAAGAC A G SRP14-AS1 Ensembl:ENSG00000248508 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40060670..40061157 26863196 MeRIP-seq:(Medium) rs1477313864 Functional Loss SNV dbSNP153 33..33 33 - - - 61695 RMVar_ID_61695 Human_SNP_ID_574332336 m1A Human chr15 - 40061852 40061852 40061852 CCTTCTCCAGCTCAATTCTGTAGGCCTTGACAAGAATCACCCATTTGTGGAAGCCCTCTCCTTTC CCTTCTCCAGCTCAATTCTGTAGGCCTTGACAGGAATCACCCATTTGTGGAAGCCCTCTCCTTTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40061803..40062065 26863196 MeRIP-seq:(Medium) rs1172087790 Functional Loss SNV dbSNP153 33..33 33 - - - 61696 RMVar_ID_61696 Human_SNP_ID_574332440 m1A Human chr15 - 40062468 40062467 40062469 TACCATACTCTAGGCCACTCCTGCTCATTCACAGATTTTAGTACCTGGCCCACGGTCTTCCTCTC TACCATACTCTAGGCCACTCCTGCTCATTCA__GATTTTAGTACCTGGCCCACGGTCTTCCTCTC CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40062424..40062513 26863196 MeRIP-seq:(Medium) rs1035994218 Functional Loss DEL dbSNP153 32..33 33 - - - 61697 RMVar_ID_61697 Human_SNP_ID_574332482 m1A Human chr15 + 40062659 40062658 40062660 CCTCCAGGCATACTGATGTGGAAGAAGAAAACAGAGCCAAGACAGGAGGTGGCTGCAAGGAAGCT CCTCCAGGCATACTGATGTGGAAGAAGAAAAC__AGCCAAGACAGGAGGTGGCTGCAAGGAAGCT CAG C SRP14-AS1 Ensembl:ENSG00000248508 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40062613..40062784 26863196 MeRIP-seq:(Medium) rs956914228 Functional Loss DEL dbSNP153 33..34 33 - - - 61698 RMVar_ID_61698 Human_SNP_ID_574332483 m1A Human chr15 + 40062659 40062659 40062659 CCTCCAGGCATACTGATGTGGAAGAAGAAAACAGAGCCAAGACAGGAGGTGGCTGCAAGGAAGCT CCTCCAGGCATACTGATGTGGAAGAAGAAAACTGAGCCAAGACAGGAGGTGGCTGCAAGGAAGCT A T SRP14-AS1 Ensembl:ENSG00000248508 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40062613..40062784 26863196 MeRIP-seq:(Medium) rs1471796604 Functional Loss SNV dbSNP153 33..33 33 - - - 61699 RMVar_ID_61699 Human_SNP_ID_574345228 m1A Human chr15 + 40108654 40108654 40108654 ACCCCAGCGCCCCAGTTCTTCATGGTCACCCCAGACGTCCGCAGCCCAAACCCTTCCCGGGCCCC ACCCCAGCGCCCCAGTTCTTCATGGTCACCCCGGACGTCCGCAGCCCAAACCCTTCCCGGGCCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:40108652..40108792 26863196 MeRIP-seq:(Medium) rs1037373709 Functional Loss SNV dbSNP153 33..33 33 - - - 61700 RMVar_ID_61700 Human_SNP_ID_574358690 m1A Human chr15 - 40161126 40161126 40161126 TGGGCTTTCTTCCGCAACCTGCCCTCGGAGCTACAGAAGCGACCAAGGCACGTACACGACTCCCT TGGGCTTTCTTCCGCAACCTGCCCTCGGAGCTGCAGAAGCGACCAAGGCACGTACACGACTCCCT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:40161051..40165069 26863196 MeRIP-seq:(Medium) rs375434078 Functional Loss SNV dbSNP153 33..33 33 - - - 61701 RMVar_ID_61701 Human_SNP_ID_574359609 m1A Human chr15 + 40165056 40165056 40165056 GAGATTTACATTTGTTTCCTTCTTCACAGTGAAGCCATGTCCCTGGAGGGAGATGAATGGGAACT GAGATTTACATTTGTTTCCTTCTTCACAGTGAGGCCATGTCCCTGGAGGGAGATGAATGGGAACT A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40165051..40165150 26863196 MeRIP-seq:(Medium) rs1324135738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885372,Human_RBP_ID_3945346,Human_RBP_ID_4319043,Human_RBP_ID_18981348,Human_RBP_ID_22047385,Human_RBP_ID_22928353,Human_RBP_ID_25183686,Human_RBP_ID_26326483,Human_RBP_ID_27809307 Human_Splice_Rec_1583490,Human_Splice_Rec_1583498,Human_Splice_Rec_1583506,Human_Splice_Rec_1583548 RMVar_hsa_circ_57449,RMVar_hsa_circ_300862,RMVar_hsa_circ_97128,RMVar_hsa_circ_170865 61702 RMVar_ID_61702 Human_SNP_ID_574364632 m1A Human chr15 + 40185377 40185377 40185377 GCCCTTGGAACACAGGCAGGTCCTTGGAACACAGGGTAAGGACTCTTAGATCCAGTGCTTTGCTG GCCCTTGGAACACAGGCAGGTCCTTGGAACACCGGGTAAGGACTCTTAGATCCAGTGCTTTGCTG A C BUB1B Ensembl:ENSG00000156970 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40185343..40185418 26863196 MeRIP-seq:(Medium) rs774455318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887164,Human_RBP_ID_9370706,Human_RBP_ID_12495693,Human_RBP_ID_19067883,Human_RBP_ID_20017907,Human_RBP_ID_22934555,Human_RBP_ID_26326315,Human_RBP_ID_27810078 Human_Splice_Rec_1583515,Human_Splice_Rec_1583559 RMVar_hsa_circ_57449,RMVar_hsa_circ_7105,RMVar_hsa_circ_52119,RMVar_hsa_circ_170868,RMVar_hsa_circ_304852,RMVar_hsa_circ_309947,RMVar_hsa_circ_342156,RMVar_hsa_circ_318811,RMVar_hsa_circ_80030,RMVar_hsa_circ_170870,RMVar_hsa_circ_25011,RMVar_hsa_circ_37594,RMVar_hsa_circ_170871,RMVar_hsa_circ_288427,RMVar_hsa_circ_350386,RMVar_hsa_circ_376054,RMVar_hsa_circ_290523,RMVar_hsa_circ_50270,RMVar_hsa_circ_170872,RMVar_hsa_circ_170873,RMVar_hsa_circ_170874,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_292405,RMVar_hsa_circ_170875 61703 RMVar_ID_61703 Human_SNP_ID_574364633 m1A Human chr15 + 40185377 40185377 40185377 GCCCTTGGAACACAGGCAGGTCCTTGGAACACAGGGTAAGGACTCTTAGATCCAGTGCTTTGCTG GCCCTTGGAACACAGGCAGGTCCTTGGAACACGGGGTAAGGACTCTTAGATCCAGTGCTTTGCTG A G BUB1B Ensembl:ENSG00000156970 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40185343..40185418 26863196 MeRIP-seq:(Medium) rs774455318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887164,Human_RBP_ID_9370706,Human_RBP_ID_12495693,Human_RBP_ID_19067883,Human_RBP_ID_20017907,Human_RBP_ID_22934555,Human_RBP_ID_26326315,Human_RBP_ID_27810078 Human_Splice_Rec_1583515,Human_Splice_Rec_1583559 RMVar_hsa_circ_57449,RMVar_hsa_circ_7105,RMVar_hsa_circ_52119,RMVar_hsa_circ_170868,RMVar_hsa_circ_304852,RMVar_hsa_circ_309947,RMVar_hsa_circ_342156,RMVar_hsa_circ_318811,RMVar_hsa_circ_80030,RMVar_hsa_circ_170870,RMVar_hsa_circ_25011,RMVar_hsa_circ_37594,RMVar_hsa_circ_170871,RMVar_hsa_circ_288427,RMVar_hsa_circ_350386,RMVar_hsa_circ_376054,RMVar_hsa_circ_290523,RMVar_hsa_circ_50270,RMVar_hsa_circ_170872,RMVar_hsa_circ_170873,RMVar_hsa_circ_170874,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_292405,RMVar_hsa_circ_170875 61704 RMVar_ID_61704 Human_SNP_ID_574364727 m1A Human chr15 + 40185641 40185641 40185641 CATATGTGGAAGAGACTGCACGACAGCCAGTTATGTGAGTGTGGTTTTTGGATATTTTGAAGTGG CATATGTGGAAGAGACTGCACGACAGCCAGTTTTGTGAGTGTGGTTTTTGGATATTTTGAAGTGG A T BUB1B Ensembl:ENSG00000156970 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:40185601..40185650 32194978 MeRIP-seq:(Medium) rs767779974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19067098,Human_RBP_ID_23650114 Human_Splice_Rec_1583516,Human_Splice_Rec_1583517,Human_Splice_Rec_1583560,Human_Splice_Rec_1583561,Human_Splice_Rec_1583605,Human_Splice_Rec_1583609 RMVar_hsa_circ_57449,RMVar_hsa_circ_7105,RMVar_hsa_circ_52119,RMVar_hsa_circ_170868,RMVar_hsa_circ_304852,RMVar_hsa_circ_309947,RMVar_hsa_circ_342156,RMVar_hsa_circ_318811,RMVar_hsa_circ_80030,RMVar_hsa_circ_170870,RMVar_hsa_circ_25011,RMVar_hsa_circ_37594,RMVar_hsa_circ_170871,RMVar_hsa_circ_288427,RMVar_hsa_circ_350386,RMVar_hsa_circ_376054,RMVar_hsa_circ_290523,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170873,RMVar_hsa_circ_170874,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_292405,RMVar_hsa_circ_170875,RMVar_hsa_circ_18787 61705 RMVar_ID_61705 Human_SNP_ID_574385127 m1A Human chr15 + 40266417 40266417 40266417 AAGACCCGGGAGAGCAGCCTGAAGCGCAGGCTATTCCGAAGCATGTTCCTGTCCACTGCTGCCAC AAGACCCGGGAGAGCAGCCTGAAGCGCAGGCTGTTCCGAAGCATGTTCCTGTCCACTGCTGCCAC A G PAK6 Ensembl:ENSG00000137843 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40266370..40266449 26863196 MeRIP-seq:(Medium) rs1460491478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1583633,Human_Splice_Rec_1583653,Human_Splice_Rec_1583673,Human_Splice_Rec_1583707,Human_Splice_Rec_1583725,Human_Splice_Rec_1583745,Human_Splice_Rec_1583809,Human_Splice_Rec_1583823 RMVar_hsa_circ_18616 61706 RMVar_ID_61706 Human_SNP_ID_574389533 m1A Human chr15 - 40281484 40281484 40281484 GTCTGTCTCGGTGCCTGGGCCGAACCCTTGGCAGGCGGGCACCGAGGCTGTGGTGCTGCGTGCTC GTCTGTCTCGGTGCCTGGGCCGAACCCTTGGCGGGCGGGCACCGAGGCTGTGGTGCTGCGTGCTC T C ANKRD63,PLCB2 Ensembl:ENSG00000230778,Ensembl:ENSG00000137841 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:40281407..40281493 26863410 MeRIP-seq:(Medium) rs1004148931 Functional Loss SNV dbSNP153 33..33 33 - - - 61707 RMVar_ID_61707 Human_SNP_ID_574390108 m1A Human chr15 - 40282814 40282813 40282814 GGAGTAGCGAGCAATCAACACCTCCAGGCGGGAGGCCCGGGGAAGGAGCGGCGACACGCCAGGCG GGAGTAGCGAGCAATCAACACCTCCAGGCGGG_GGCCCGGGGAAGGAGCGGCGACACGCCAGGCG CT C PLCB2 Ensembl:ENSG00000137841 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40282718..40283019 26863196 MeRIP-seq:(Medium) rs1485943194 Functional Loss DEL dbSNP153 33..33 33 - - - 61708 RMVar_ID_61708 Human_SNP_ID_574391674 m1A Human chr15 - 40288890 40288890 40288890 ACAGTTCCAGAAGGAGGCGCTGGCAGAGTACGAGGCCAGGATGAAGGGTCTGGAGGCAGAGGTGA ACAGTTCCAGAAGGAGGCGCTGGCAGAGTACGTGGCCAGGATGAAGGGTCTGGAGGCAGAGGTGA T A PLCB2 Ensembl:ENSG00000137841 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40288761..40288933 26863196 MeRIP-seq:(Medium) rs763121112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1583858,Human_Splice_Rec_1583860,Human_Splice_Rec_1583914,Human_Splice_Rec_1583974,Human_Splice_Rec_1584034,Human_Splice_Rec_1584092 61709 RMVar_ID_61709 Human_SNP_ID_574391675 m1A Human chr15 - 40288890 40288890 40288890 ACAGTTCCAGAAGGAGGCGCTGGCAGAGTACGAGGCCAGGATGAAGGGTCTGGAGGCAGAGGTGA ACAGTTCCAGAAGGAGGCGCTGGCAGAGTACGGGGCCAGGATGAAGGGTCTGGAGGCAGAGGTGA T C PLCB2 Ensembl:ENSG00000137841 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40288761..40288933 26863196 MeRIP-seq:(Medium) rs763121112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1583858,Human_Splice_Rec_1583860,Human_Splice_Rec_1583914,Human_Splice_Rec_1583974,Human_Splice_Rec_1584034,Human_Splice_Rec_1584092 61710 RMVar_ID_61710 Human_SNP_ID_574391806 m1A Human chr15 + 40289324 40289312 40289324 TCTGTTCCAGGCAAGCCGCCTGCTTCTCCTCCAGCTTCTCCTGGTGCCTCTCCAAGTTCTCCGTC TCTGTTCCAGGCAAGCCGCCT____________GCTTCTCCTGGTGCCTCTCCAAGTTCTCCGTC TGCTTCTCCTCCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40289216..40289409 26863196 MeRIP-seq:(Medium) rs763532703 Functional Loss DEL dbSNP153 22..33 33 - - - 61711 RMVar_ID_61711 Human_SNP_ID_574391808 m1A Human chr15 - 40289318 40289316 40289319 GAACTTGGAGAGGCACCAGGAGAAGCTGGAGGAGAAGCAGGCGGCTTGCCTGGAACAGATACGGG GAACTTGGAGAGGCACCAGGAGAAGCTGGAG___AAGCAGGCGGCTTGCCTGGAACAGATACGGG TCTC T PLCB2 Ensembl:ENSG00000137841 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40289291..40289375 26863196 MeRIP-seq:(Medium) rs1370199518 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_884144,Human_RBP_ID_26326496 Human_Splice_Rec_1583839,Human_Splice_Rec_1583846,Human_Splice_Rec_1583847,Human_Splice_Rec_1583856,Human_Splice_Rec_1583857,Human_Splice_Rec_1583859,Human_Splice_Rec_1583912,Human_Splice_Rec_1583913,Human_Splice_Rec_1583972,Human_Splice_Rec_1583973,Human_Splice_Rec_1584032,Human_Splice_Rec_1584033,Human_Splice_Rec_1584090,Human_Splice_Rec_1584091,Human_Splice_Rec_1584098,Human_Splice_Rec_1584099,Human_Splice_Rec_1584106 RMVar_hsa_circ_72458 61712 RMVar_ID_61712 Human_SNP_ID_574392294 m1A Human chr15 - 40290606 40290604 40290607 AAGAGACTGGAGCGGATCCAGGGCATGACCAAAGTCACCACAGACAAGATGGCCCAGGAGAGGTG AAGAGACTGGAGCGGATCCAGGGCATGACCA___TCACCACAGACAAGATGGCCCAGGAGAGGTG ACTT A PLCB2 Ensembl:ENSG00000137841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40290604..40290705 26863196 MeRIP-seq:(Medium) rs774940043 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1583843,Human_Splice_Rec_1583852,Human_Splice_Rec_1583853,Human_Splice_Rec_1583910,Human_Splice_Rec_1583911,Human_Splice_Rec_1583968,Human_Splice_Rec_1583969,Human_Splice_Rec_1584028,Human_Splice_Rec_1584029,Human_Splice_Rec_1584086,Human_Splice_Rec_1584087,Human_Splice_Rec_1584095,Human_Splice_Rec_1584103 RMVar_hsa_circ_72458 61713 RMVar_ID_61713 Human_SNP_ID_574392295 m1A Human chr15 - 40290606 40290606 40290606 AAGAGACTGGAGCGGATCCAGGGCATGACCAAAGTCACCACAGACAAGATGGCCCAGGAGAGGTG AAGAGACTGGAGCGGATCCAGGGCATGACCAAGGTCACCACAGACAAGATGGCCCAGGAGAGGTG T C PLCB2 Ensembl:ENSG00000137841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40290604..40290705 26863196 MeRIP-seq:(Medium) rs1433501881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1583843,Human_Splice_Rec_1583852,Human_Splice_Rec_1583853,Human_Splice_Rec_1583910,Human_Splice_Rec_1583911,Human_Splice_Rec_1583968,Human_Splice_Rec_1583969,Human_Splice_Rec_1584028,Human_Splice_Rec_1584029,Human_Splice_Rec_1584086,Human_Splice_Rec_1584087,Human_Splice_Rec_1584095,Human_Splice_Rec_1584103 RMVar_hsa_circ_72458 61714 RMVar_ID_61714 Human_SNP_ID_574392514 m1A Human chr15 - 40291067 40291067 40291067 CAGGCTGGAGCTGGAGCTGCTGCGGCAGGGCGAGGAGCAGTACGAGTGCGTTCTGAAGCGCAAGG CAGGCTGGAGCTGGAGCTGCTGCGGCAGGGCGGGGAGCAGTACGAGTGCGTTCTGAAGCGCAAGG T C PLCB2 Ensembl:ENSG00000137841 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40289558..40291478 26863196 MeRIP-seq:(Medium) rs1349261010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1583849,Human_Splice_Rec_1583907,Human_Splice_Rec_1583965,Human_Splice_Rec_1584025,Human_Splice_Rec_1584083 61715 RMVar_ID_61715 Human_SNP_ID_574401472 m1A Human chr15 + 40323721 40323721 40323721 GCCACTGGAGACCAGGCGGCCGGCGGCCGGGCAGGCGGCGGCGGAGCGCGCGGCGGCGTGGCGGC GCCACTGGAGACCAGGCGGCCGGCGGCCGGGCGGGCGGCGGCGGAGCGCGCGGCGGCGTGGCGGC A G INAFM2 Ensembl:ENSG00000259330 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40323693..40323822 26863196 MeRIP-seq:(Medium) rs970623444 Functional Loss SNV dbSNP153 33..33 33 - - - 61716 RMVar_ID_61716 Human_SNP_ID_574401525 m1A Human chr15 - 40323852 40323834 40323852 CGCCGCCGGGGCCTGGACCAGTCACCGCCGCCAGCGCCGCCGCCGCCGCCGGCCCGTCAGCTGCT CGCCGCCGGGGCCTGGACCAGTCACCGCCGCC__________________GGCCCGTCAGCTGCT CGGCGGCGGCGGCGGCGCT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:40323761..40323910 26863410 MeRIP-seq:(Medium) rs902716960 Functional Loss DEL dbSNP153 33..50 33 - - - 61717 RMVar_ID_61717 Human_SNP_ID_574404649 m1A Human chr15 - 40335812 40335812 40335812 TGAGCTGTGTTTCTACAGGTGGGATATGAAGGAAGACAAGGAGGAGCTGGAAGGTCAGGAGGTAG TGAGCTGTGTTTCTACAGGTGGGATATGAAGGGAGACAAGGAGGAGCTGGAAGGTCAGGAGGTAG T C CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40335503..40336842 26863196 MeRIP-seq:(Medium) rs768414232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584150,Human_Splice_Rec_1584151,Human_Splice_Rec_1584164,Human_Splice_Rec_1584165,Human_Splice_Rec_1584184,Human_Splice_Rec_1584185,Human_Splice_Rec_1584192,Human_Splice_Rec_1584193 61718 RMVar_ID_61718 Human_SNP_ID_574405279 m1A Human chr15 - 40337802 40337802 40337802 TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGACCTAGCCCGCCTCGCCCGGCACAGAGACGCAC TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGTCCTAGCCCGCCTCGCCCGGCACAGAGACGCAC T A CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40337438..40337915 26863196 MeRIP-seq:(Medium) rs1019233835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584142,Human_Splice_Rec_1584143,Human_Splice_Rec_1584156,Human_Splice_Rec_1584157,Human_Splice_Rec_1584176,Human_Splice_Rec_1584177,Human_Splice_Rec_1584187,Human_Splice_Rec_1584200,Human_Splice_Rec_1584201,Human_Splice_Rec_1584210 RMVar_hsa_circ_34019,RMVar_hsa_circ_34431 61719 RMVar_ID_61719 Human_SNP_ID_574405280 m1A Human chr15 - 40337802 40337802 40337802 TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGACCTAGCCCGCCTCGCCCGGCACAGAGACGCAC TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGGCCTAGCCCGCCTCGCCCGGCACAGAGACGCAC T C CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40337438..40337915 26863196 MeRIP-seq:(Medium) rs1019233835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584142,Human_Splice_Rec_1584143,Human_Splice_Rec_1584156,Human_Splice_Rec_1584157,Human_Splice_Rec_1584176,Human_Splice_Rec_1584177,Human_Splice_Rec_1584187,Human_Splice_Rec_1584200,Human_Splice_Rec_1584201,Human_Splice_Rec_1584210 RMVar_hsa_circ_34019,RMVar_hsa_circ_34431 61720 RMVar_ID_61720 Human_SNP_ID_574405281 m1A Human chr15 - 40337802 40337802 40337802 TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGACCTAGCCCGCCTCGCCCGGCACAGAGACGCAC TGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGCCCTAGCCCGCCTCGCCCGGCACAGAGACGCAC T G CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40337438..40337915 26863196 MeRIP-seq:(Medium) rs1019233835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584142,Human_Splice_Rec_1584143,Human_Splice_Rec_1584156,Human_Splice_Rec_1584157,Human_Splice_Rec_1584176,Human_Splice_Rec_1584177,Human_Splice_Rec_1584187,Human_Splice_Rec_1584200,Human_Splice_Rec_1584201,Human_Splice_Rec_1584210 RMVar_hsa_circ_34019,RMVar_hsa_circ_34431 61721 RMVar_ID_61721 Human_SNP_ID_574405652 m1A Human chr15 - 40338888 40338888 40338888 GGGTCTTTGTTCTGCAGGAAAAGCGGGTGGTTAGCAGGAACTGGGCAAGGGGTACCTGTGGACCC GGGTCTTTGTTCTGCAGGAAAAGCGGGTGGTTTGCAGGAACTGGGCAAGGGGTACCTGTGGACCC T A CCDC9B Ensembl:ENSG00000188549 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40338556..40338942 32194978 MeRIP-seq:(Medium) rs1566908321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584172,Human_Splice_Rec_1584206 61722 RMVar_ID_61722 Human_SNP_ID_574406044 m1A Human chr15 - 40339975 40339973 40339976 CAGAGCCGAGTCCCCCATGAGCAGGCAGGAGAAGGACGCAGAGCTGGATCGGAGGATAGTTGCCC CAGAGCCGAGTCCCCCATGAGCAGGCAGGAG___GACGCAGAGCTGGATCGGAGGATAGTTGCCC CCTT C CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40339865..40340036 26863196 MeRIP-seq:(Medium) rs755440406 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5566281,Human_RBP_ID_19067101 Human_Splice_Rec_1584168,Human_Splice_Rec_1584169,Human_Splice_Rec_1584195,Human_Splice_Rec_1584203,Human_Splice_Rec_1584212,Human_Splice_Rec_1584213 61723 RMVar_ID_61723 Human_SNP_ID_574406300 m1A Human chr15 + 40340875 40340875 40340875 TTCCAGAGCAGCCCCTGGGGAGCCAGAGTGGGAGGAAAGCTGGAGCCACCGGAGCCGGGCCTCTG TTCCAGAGCAGCCCCTGGGGAGCCAGAGTGGGTGGAAAGCTGGAGCCACCGGAGCCGGGCCTCTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40340772..40340906 26863196 MeRIP-seq:(Medium) rs1484057471 Functional Loss SNV dbSNP153 33..33 33 - - - 61724 RMVar_ID_61724 Human_SNP_ID_574406315 m1A Human chr15 - 40340904 40340904 40340904 GAGCAGCGAAGCCGGCAGGGAGAGGCCGGCAGAGGCCCGGCTCCGGTGGCTCCAGCTTTCCTCCC GAGCAGCGAAGCCGGCAGGGAGAGGCCGGCAGGGGCCCGGCTCCGGTGGCTCCAGCTTTCCTCCC T C CCDC9B Ensembl:ENSG00000188549 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40340819..40340922 26863196 MeRIP-seq:(Medium) rs748562160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584167,Human_Splice_Rec_1584211 61725 RMVar_ID_61725 Human_SNP_ID_574410878 m1A Human chr15 + 40358254 40358233 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACC_____________________CCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CCCGCCGCCGCTGCCGCCGCCA C DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs1329522686 Functional Loss DEL dbSNP153 13..33 33 - - - 61726 RMVar_ID_61726 Human_SNP_ID_574410888 m1A Human chr15 + 40358254 40358236 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACCCCG__________________CCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA GCCGCCGCTGCCGCCGCCA G DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs1158486049 Functional Loss DEL dbSNP153 16..33 33 - - - 61727 RMVar_ID_61727 Human_SNP_ID_574410895 m1A Human chr15 + 40358254 40358242 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACCCCGCCGCCG____________CCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA GCTGCCGCCGCCA G DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs1303760636 Functional Loss DEL dbSNP153 22..33 33 - - - 61728 RMVar_ID_61728 Human_SNP_ID_574410917 m1A Human chr15 + 40358254 40358245 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACCCCGCCGCCGCTG_________CCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA GCCGCCGCCA G DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs905655501 Functional Loss DEL dbSNP153 25..33 33 - - - 61729 RMVar_ID_61729 Human_SNP_ID_574410930 m1A Human chr15 + 40358254 40358251 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACCCCGCCGCCGCTGCCGCCG___CCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA GCCA G DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs1198317254 Functional Loss DEL dbSNP153 31..33 33 - - - 61730 RMVar_ID_61730 Human_SNP_ID_574410935 m1A Human chr15 + 40358254 40358254 40358254 CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA CGCACGAGCACCCCGCCGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGGCTTCA A G DISP2 Ensembl:ENSG00000140323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr15:40358206..40358310;chr15:40358162..40358354 26863196 MeRIP-seq:(Medium) rs1214634679 Functional Loss SNV dbSNP153 33..33 33 - - - 61731 RMVar_ID_61731 Human_SNP_ID_574414197 m1A Human chr15 - 40369025 40369025 40369025 CCCAGGAGCAGTGTGGCAAAGGCCAGCGCCAAAGCCAGGCCCAGCACCACAGCAGGCTCAGTGCT CCCAGGAGCAGTGTGGCAAAGGCCAGCGCCAATGCCAGGCCCAGCACCACAGCAGGCTCAGTGCT T A AC013356.4 Ensembl:ENSG00000259368 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40368924..40369124 32194978 MeRIP-seq:(Medium) rs1036114213 Functional Loss SNV dbSNP153 33..33 33 - - - 61732 RMVar_ID_61732 Human_SNP_ID_574417987 m1A Human chr15 + 40383005 40383005 40383005 CACGACAGTTGCTGCAGGGAATCTTTTAAACGAGAGCGAGAAGGACTGCGGGCAGGACCGGCGGG CACGACAGTTGCTGCAGGGAATCTTTTAAACGTGAGCGAGAAGGACTGCGGGCAGGACCGGCGGG A T KNSTRN Ensembl:ENSG00000128944 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40382951..40383325 26863196 MeRIP-seq:(Medium) rs1194398709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3473467,Human_RBP_ID_4319276,Human_RBP_ID_6422266,Human_RBP_ID_9324221 Human_Splice_Rec_1584241,Human_Splice_Rec_1584243,Human_Splice_Rec_1584259,Human_Splice_Rec_1584275,Human_Splice_Rec_1584291,Human_Splice_Rec_1584305,Human_Splice_Rec_1584321,Human_Splice_Rec_1584325,Human_Splice_Rec_1584341,Human_Splice_Rec_1584347,Human_Splice_Rec_1584365,Human_Splice_Rec_1584381,Human_Splice_Rec_1584393,Human_Splice_Rec_1584403 61733 RMVar_ID_61733 Human_SNP_ID_574418111 m1A Human chr15 - 40383302 40383302 40383302 TTGGACCCTCACCTGCCGGCTGGCCGCCGCTCAGCGCAGAGGGGGGCTGCAGGCTATACACTGTC TTGGACCCTCACCTGCCGGCTGGCCGCCGCTCGGCGCAGAGGGGGGCTGCAGGCTATACACTGTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:40383077..40383358 26863196 MeRIP-seq:(Medium) rs1476690636 Functional Loss SNV dbSNP153 33..33 33 - - - 61734 RMVar_ID_61734 Human_SNP_ID_574418836 m1A Human chr15 + 40386313 40386313 40386313 TCGAATGGGGCTCTGTTTGTTACAGGGTTGCAACTGTCGGGTCATGATGCCAGAAGCTTTACCTC TCGAATGGGGCTCTGTTTGTTACAGGGTTGCAGCTGTCGGGTCATGATGCCAGAAGCTTTACCTC A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40386310..40386475 26863196 MeRIP-seq:(Medium) rs199948606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3473476,Human_RBP_ID_8803788 RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889 61735 RMVar_ID_61735 Human_SNP_ID_574418837 m1A Human chr15 + 40386313 40386313 40386313 TCGAATGGGGCTCTGTTTGTTACAGGGTTGCAACTGTCGGGTCATGATGCCAGAAGCTTTACCTC TCGAATGGGGCTCTGTTTGTTACAGGGTTGCATCTGTCGGGTCATGATGCCAGAAGCTTTACCTC A T KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40386310..40386475 26863196 MeRIP-seq:(Medium) rs199948606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3473476,Human_RBP_ID_8803788 RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889 61736 RMVar_ID_61736 Human_SNP_ID_574418844 m1A Human chr15 + 40386324 40386324 40386324 TCTGTTTGTTACAGGGTTGCAACTGTCGGGTCATGATGCCAGAAGCTTTACCTCTCATTTTCCTT TCTGTTTGTTACAGGGTTGCAACTGTCGGGTCTTGATGCCAGAAGCTTTACCTCTCATTTTCCTT A T KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40386322..40386450 26863196 MeRIP-seq:(Medium) rs367716458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8803788,Human_RBP_ID_25135637 RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889 61737 RMVar_ID_61737 Human_SNP_ID_574422395 m1A Human chr15 + 40399393 40399393 40399393 AGGGAAGAATACCACATATGTAAAGTGTACTCAACGCATCATATTGAGAGGTGAAGCCAGCTGGA AGGGAAGAATACCACATATGTAAAGTGTACTCCACGCATCATATTGAGAGGTGAAGCCAGCTGGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:40399360..40399487 26863196 MeRIP-seq:(Medium) rs1285229233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456591,Human_RBP_ID_12497379,Human_RBP_ID_23650247 61738 RMVar_ID_61738 Human_SNP_ID_574422396 m1A Human chr15 + 40399393 40399393 40399393 AGGGAAGAATACCACATATGTAAAGTGTACTCAACGCATCATATTGAGAGGTGAAGCCAGCTGGA AGGGAAGAATACCACATATGTAAAGTGTACTCGACGCATCATATTGAGAGGTGAAGCCAGCTGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:40399360..40399487 26863196 MeRIP-seq:(Medium) rs1285229233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456591,Human_RBP_ID_12497379,Human_RBP_ID_23650247 61739 RMVar_ID_61739 Human_SNP_ID_574424242 m1A Human chr15 - 40405902 40405902 40405902 TCCACGGGCAAAAGCGAGTGGGCCCGCTGGGAAACGAAGCCGGCAAGCGGCGGCCGCAGCCTCCA TCCACGGGCAAAAGCGAGTGGGCCCGCTGGGAGACGAAGCCGGCAAGCGGCGGCCGCAGCCTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40405854..40405922 26863196 MeRIP-seq:(Medium) rs548882436 Functional Loss SNV dbSNP153 33..33 33 - - - 61740 RMVar_ID_61740 Human_SNP_ID_574433231 m1A Human chr15 + 40440289 40440289 40440289 GAGCCAGGACCGACCTTGCTGGAAAGGAAAGGAGACGTGGCAGGCAGGGAAGTCGGAAAGATGAG GAGCCAGGACCGACCTTGCTGGAAAGGAAAGGGGACGTGGCAGGCAGGGAAGTCGGAAAGATGAG A G BAHD1 Ensembl:ENSG00000140320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40440164..40440312 26863196 MeRIP-seq:(Medium) rs1288819643 Functional Loss SNV dbSNP153 33..33 33 - - - 61741 RMVar_ID_61741 Human_SNP_ID_574433605 m1A Human chr15 - 40441251 40441242 40441251 CGGCCCCTGACTCACCAGAACGGGCGGCGCGGACGGCGCGGCTCTGGGCGCCCGCAGGCCCCGGC CGGCCCCTGACTCACCAGAACGGGCGGCGCGG_________CTCTGGGCGCCCGCAGGCCCCGGC GCCGCGCCGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40441002..40441342 26863196 MeRIP-seq:(Medium) rs1301153536 Functional Loss DEL dbSNP153 33..41 33 - - - 61742 RMVar_ID_61742 Human_SNP_ID_574438110 m1A Human chr15 + 40458552 40458552 40458552 GCCGAGAGCCCCTGCAGATGGAAGACAGCAACATGGAGCAGGGGGTTGAGGGTGTGGAGCCAGGC GCCGAGAGCCCCTGCAGATGGAAGACAGCAACGTGGAGCAGGGGGTTGAGGGTGTGGAGCCAGGC A G BAHD1 Ensembl:ENSG00000140320 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40458501..40458629 26863196 MeRIP-seq:(Medium) rs770567434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4344555,Human_RBP_ID_9283969 Human_miRNA_ID_2660390 RMVar_hsa_circ_14807,RMVar_hsa_circ_99408,RMVar_hsa_circ_338819,RMVar_hsa_circ_170907,RMVar_hsa_circ_170908 61743 RMVar_ID_61743 Human_SNP_ID_574438120 m1A Human chr15 + 40458577 40458577 40458577 CAGCAACATGGAGCAGGGGGTTGAGGGTGTGGAGCCAGGCATGCCCGAGAGCCCAGGTCACCTCA CAGCAACATGGAGCAGGGGGTTGAGGGTGTGGGGCCAGGCATGCCCGAGAGCCCAGGTCACCTCA A G BAHD1 Ensembl:ENSG00000140320 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40458526..40458630 26863196 MeRIP-seq:(Medium) rs1237193327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9283969 Human_miRNA_ID_335545,Human_miRNA_ID_2083818 RMVar_hsa_circ_14807,RMVar_hsa_circ_99408,RMVar_hsa_circ_338819,RMVar_hsa_circ_170907,RMVar_hsa_circ_170908 61744 RMVar_ID_61744 Human_SNP_ID_574439339 m1A Human chr15 - 40462231 40462225 40462231 CCAACAGGTACCCAGCCATTAGTGCGGCGGCGACGGCGGCGGCGAGGGCGTGGGCGCTGGACACG CCAACAGGTACCCAGCCATTAGTGCGGCGGCG______GCGGCGAGGGCGTGGGCGCTGGACACG CCGCCGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40461990..40462234 26863196 MeRIP-seq:(Medium) rs759073538 Functional Loss DEL dbSNP153 33..38 33 - - - 61745 RMVar_ID_61745 Human_SNP_ID_574439349 m1A Human chr15 - 40462231 40462231 40462231 CCAACAGGTACCCAGCCATTAGTGCGGCGGCGACGGCGGCGGCGAGGGCGTGGGCGCTGGACACG CCAACAGGTACCCAGCCATTAGTGCGGCGGCGGCGGCGGCGGCGAGGGCGTGGGCGCTGGACACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40461990..40462234 26863196 MeRIP-seq:(Medium) rs762888298 Functional Loss SNV dbSNP153 33..33 33 - - - 61746 RMVar_ID_61746 Human_SNP_ID_574440345 m1A Human chr15 + 40465992 40465992 40465992 CGCCGAGGTGAAGGCCTCCCCAGCCGAAAGACAGCACTGGTTCCCCCCTCTGCAGACTATTCCAC CGCCGAGGTGAAGGCCTCCCCAGCCGAAAGACGGCACTGGTTCCCCCCTCTGCAGACTATTCCAC A G BAHD1 Ensembl:ENSG00000140320 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40465943..40466044 32194978 MeRIP-seq:(Medium) rs955400923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6422550,Human_RBP_ID_27434604 Human_Splice_Rec_1584608,Human_Splice_Rec_1584620,Human_Splice_Rec_1584630,Human_Splice_Rec_1584632 Human_miRNA_ID_1511312 61747 RMVar_ID_61747 Human_SNP_ID_574441767 m1A Human chr15 + 40471073 40471073 40471073 TCGGCGCCGCAGCCCGGGAGCCGGCCACCCCTACACGCGCCAGGGCTGTCCCCTGCCCTCCCCTC TCGGCGCCGCAGCCCGGGAGCCGGCCACCCCTGCACGCGCCAGGGCTGTCCCCTGCCCTCCCCTC A G CHST14 Ensembl:ENSG00000169105 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40471028..40471271 26863196 MeRIP-seq:(Medium) rs1474067619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4319591,Human_RBP_ID_27434609 61748 RMVar_ID_61748 Human_SNP_ID_574441776 m1A Human chr15 - 40471099 40471099 40471099 AGGGTCTGGGACCGGGGGTAGTTGGGGAGGGGAGGGCAGGGGACAGCCCTGGCGCGTGTAGGGGT AGGGTCTGGGACCGGGGGTAGTTGGGGAGGGGGGGGCAGGGGACAGCCCTGGCGCGTGTAGGGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:40471001..40471207 26863410 MeRIP-seq:(Medium) rs1433261749 Functional Loss SNV dbSNP153 33..33 33 - - - 61749 RMVar_ID_61749 Human_SNP_ID_574441780 m1A Human chr15 - 40471104 40471104 40471104 GGAGGAGGGTCTGGGACCGGGGGTAGTTGGGGAGGGGAGGGCAGGGGACAGCCCTGGCGCGTGTA GGAGGAGGGTCTGGGACCGGGGGTAGTTGGGGGGGGGAGGGCAGGGGACAGCCCTGGCGCGTGTA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:40471008..40471107 26863410 MeRIP-seq:(Medium) rs1463164193 Functional Loss SNV dbSNP153 33..33 33 - - - 61750 RMVar_ID_61750 Human_SNP_ID_574441781 m1A Human chr15 - 40471104 40471104 40471104 GGAGGAGGGTCTGGGACCGGGGGTAGTTGGGGAGGGGAGGGCAGGGGACAGCCCTGGCGCGTGTA GGAGGAGGGTCTGGGACCGGGGGTAGTTGGGGCGGGGAGGGCAGGGGACAGCCCTGGCGCGTGTA T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:40471008..40471107 26863410 MeRIP-seq:(Medium) rs1463164193 Functional Loss SNV dbSNP153 33..33 33 - - - 61751 RMVar_ID_61751 Human_SNP_ID_574442281 m1A Human chr15 + 40472237 40472237 40472237 CCAGCCCCGAAAGCCTGCATTACCACTTGTGCAGTGCCCCCCGGGCCCTGCTGCAGGATGTGCTG CCAGCCCCGAAAGCCTGCATTACCACTTGTGCGGTGCCCCCCGGGCCCTGCTGCAGGATGTGCTG A G CHST14 Ensembl:ENSG00000169105 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40471940..40472239 32194978 MeRIP-seq:(Medium) rs775530263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456638,Human_RBP_ID_22439967,Human_RBP_ID_22759196 61752 RMVar_ID_61752 Human_SNP_ID_574444294 m1A Human chr15 - 40480934 40480934 40480934 TTTCTTGGGTGAAAAATACATCCGCAGGGTTCAGATGAGACCAGGTGTTGCTTGTTCAGTATCTC TTTCTTGGGTGAAAAATACATCCGCAGGGTTCCGATGAGACCAGGTGTTGCTTGTTCAGTATCTC T G AC013356.1 Ensembl:ENSG00000244251 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs565579744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17871006 61753 RMVar_ID_61753 Human_SNP_ID_574460931 m1A Human chr15 + 40549449 40549449 40549449 TCTTCTATTTCCTCTCACTCCTATTCATTTCTATGGACTCAGCTCCCCTAACACGGCCTCTCTCC TCTTCTATTTCCTCTCACTCCTATTCATTTCTCTGGACTCAGCTCCCCTAACACGGCCTCTCTCC A C AC091045.2 Ensembl:ENSG00000259536 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40549322..40549517 26863196 MeRIP-seq:(Medium) rs981111600 Functional Loss SNV dbSNP153 33..33 33 - - - 61754 RMVar_ID_61754 Human_SNP_ID_574460932 m1A Human chr15 + 40549449 40549449 40549449 TCTTCTATTTCCTCTCACTCCTATTCATTTCTATGGACTCAGCTCCCCTAACACGGCCTCTCTCC TCTTCTATTTCCTCTCACTCCTATTCATTTCTGTGGACTCAGCTCCCCTAACACGGCCTCTCTCC A G AC091045.2 Ensembl:ENSG00000259536 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40549322..40549517 26863196 MeRIP-seq:(Medium) rs981111600 Functional Loss SNV dbSNP153 33..33 33 - - - 61755 RMVar_ID_61755 Human_SNP_ID_574466103 m1A Human chr15 - 40569705 40569705 40569705 AATAACTGGTTTCTGCAAAGTGCTCATCTCCGAAGCTCACCCCGGTCCGCCGCTTCTTCGGGGGC AATAACTGGTTTCTGCAAAGTGCTCATCTCCGTAGCTCACCCCGGTCCGCCGCTTCTTCGGGGGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40569516..40569787 26863196 MeRIP-seq:(Medium) rs1388655479 Functional Loss SNV dbSNP153 33..33 33 - - - 61756 RMVar_ID_61756 Human_SNP_ID_574466104 m1A Human chr15 - 40569705 40569705 40569705 AATAACTGGTTTCTGCAAAGTGCTCATCTCCGAAGCTCACCCCGGTCCGCCGCTTCTTCGGGGGC AATAACTGGTTTCTGCAAAGTGCTCATCTCCGCAGCTCACCCCGGTCCGCCGCTTCTTCGGGGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40569516..40569787 26863196 MeRIP-seq:(Medium) rs1388655479 Functional Loss SNV dbSNP153 33..33 33 - - - 61757 RMVar_ID_61757 Human_SNP_ID_574472598 m1A Human chr15 - 40593840 40593840 40593840 CTAATCCATTGTGCTCTGCACGCGTGGGTTCGAATCCCATCCTCGTCGATGTGGTGGCTTACTTT CTAATCCATTGTGCTCTGCACGCGTGGGTTCGCATCCCATCCTCGTCGATGTGGTGGCTTACTTT T G tRNA-Ser-GCT-4-2 RNACentral:URS00002034DC tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs892554769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17368451,Human_RBP_ID_18199767,Human_RBP_ID_18662019,Human_RBP_ID_20091643,Human_RBP_ID_22798768,Human_RBP_ID_23127342,Human_RBP_ID_23677221,Human_RBP_ID_24475170,Human_RBP_ID_26748660 61758 RMVar_ID_61758 Human_SNP_ID_574501143 m1A Human chr15 + 40695247 40695247 40695247 ACCGAGCCCTAAGGAGAGTGCGGCGCTTCCCGAGGCGTGCAGCTGGGAACTGCAACTCATCTGGG ACCGAGCCCTAAGGAGAGTGCGGCGCTTCCCGGGGCGTGCAGCTGGGAACTGCAACTCATCTGGG A G RAD51 Ensembl:ENSG00000051180 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:40695196..40695341 26863196 MeRIP-seq:(Medium) rs1209685275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4319864 Human_Splice_Rec_1585035 61759 RMVar_ID_61759 Human_SNP_ID_574514987 m1A Human chr15 - 40744148 40744148 40744148 GGGGCCTCACCCGTTTCTGTCTGGTCTGCAGTATGGAAGCCGGCAGGACTTTCTCTGGCGCCTGG GGGGCCTCACCCGTTTCTGTCTGGTCTGCAGTGTGGAAGCCGGCAGGACTTTCTCTGGCGCCTGG T C RMDN3 Ensembl:ENSG00000137824 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40744049..40744199 32194978 MeRIP-seq:(Medium) rs1396249125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885401,Human_RBP_ID_4319946,Human_RBP_ID_22540532,Human_RBP_ID_22650394 Human_Splice_Rec_1585150,Human_Splice_Rec_1585184,Human_Splice_Rec_1585208,Human_Splice_Rec_1585226,Human_Splice_Rec_1585270,Human_Splice_Rec_1585282 RMVar_hsa_circ_91281,RMVar_hsa_circ_331930,RMVar_hsa_circ_170943,RMVar_hsa_circ_170947,RMVar_hsa_circ_94085,RMVar_hsa_circ_170945,RMVar_hsa_circ_170946,RMVar_hsa_circ_375747,RMVar_hsa_circ_93545,RMVar_hsa_circ_170948,RMVar_hsa_circ_370869,RMVar_hsa_circ_270174,RMVar_hsa_circ_372955,RMVar_hsa_circ_170950,RMVar_hsa_circ_170951,RMVar_hsa_circ_170949 61760 RMVar_ID_61760 Human_SNP_ID_574517139 m1A Human chr15 + 40751561 40751561 40751561 TTCGCCGCCGAGCCACTCTCTGGTTCTCTTCCATGTGGCATCTGGAAAGCAGGCCCCATCCCGAA TTCGCCGCCGAGCCACTCTCTGGTTCTCTTCCGTGTGGCATCTGGAAAGCAGGCCCCATCCCGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40751512..40752125 26863196 MeRIP-seq:(Medium) rs1165844191 Functional Loss SNV dbSNP153 33..33 33 - - - 61761 RMVar_ID_61761 Human_SNP_ID_574517244 m1A Human chr15 + 40751946 40751946 40751946 AAGGCCAGAACACACCCCAGCTGAAAAGCTGCAGGGGAGGGATAAAGCAGGAGAAGAAGCCGCAT AAGGCCAGAACACACCCCAGCTGAAAAGCTGCCGGGGAGGGATAAAGCAGGAGAAGAAGCCGCAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40751943..40752116 26863196 MeRIP-seq:(Medium) rs374145058 Functional Loss SNV dbSNP153 33..33 33 - - - 61762 RMVar_ID_61762 Human_SNP_ID_574518151 m1A Human chr15 - 40755090 40755090 40755090 AGGGCGCCGGGTTTGTGGTCTGCAGTGTCGTGAGGCTGAGGTGGGGGTTGAAGGCCCAGAAGCCG AGGGCGCCGGGTTTGTGGTCTGCAGTGTCGTGTGGCTGAGGTGGGGGTTGAAGGCCCAGAAGCCG T A RMDN3 Ensembl:ENSG00000137824 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40754601..40755250 26863196 MeRIP-seq:(Medium) rs1028219913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342238,Human_RBP_ID_8941223,Human_RBP_ID_23650536 Human_Splice_Rec_1585175,Human_Splice_Rec_1585199,Human_Splice_Rec_1585257 RMVar_hsa_circ_93545,RMVar_hsa_circ_170951 61763 RMVar_ID_61763 Human_SNP_ID_574518152 m1A Human chr15 - 40755090 40755090 40755090 AGGGCGCCGGGTTTGTGGTCTGCAGTGTCGTGAGGCTGAGGTGGGGGTTGAAGGCCCAGAAGCCG AGGGCGCCGGGTTTGTGGTCTGCAGTGTCGTGCGGCTGAGGTGGGGGTTGAAGGCCCAGAAGCCG T G RMDN3 Ensembl:ENSG00000137824 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40754601..40755250 26863196 MeRIP-seq:(Medium) rs1028219913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342238,Human_RBP_ID_8941223,Human_RBP_ID_23650536 Human_Splice_Rec_1585175,Human_Splice_Rec_1585199,Human_Splice_Rec_1585257 RMVar_hsa_circ_93545,RMVar_hsa_circ_170951 61764 RMVar_ID_61764 Human_SNP_ID_574521512 m1A Human chr15 - 40767213 40767212 40767214 CATCGACGTAGTATTCATAACTGCAAAGAGACAGGATGGGGGGGGTGAGGAGGGGCACACAGCAA CATCGACGTAGTATTCATAACTGCAAAGAGA__GGATGGGGGGGGTGAGGAGGGGCACACAGCAA CTG C DNAJC17 Ensembl:ENSG00000104129 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40767211..40767457 26863196 MeRIP-seq:(Medium) rs1459512471 Functional Loss DEL dbSNP153 32..33 33 - - - 61765 RMVar_ID_61765 Human_SNP_ID_574523311 m1A Human chr15 + 40773695 40773695 40773695 AGGAGCCCAGGTAGGAAGAGCTCCGAGACCTGAGCGCCCAGCCGGGCGAGGCCTGACTCCTCACC AGGAGCCCAGGTAGGAAGAGCTCCGAGACCTGGGCGCCCAGCCGGGCGAGGCCTGACTCCTCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40773694..40773760 26863196 MeRIP-seq:(Medium) rs896888412 Functional Loss SNV dbSNP153 33..33 33 - - - 61766 RMVar_ID_61766 Human_SNP_ID_574523756 m1A Human chr15 - 40775106 40775106 40775106 AATCAGTGTTTCATGAGGCTCTCTTTTCAGCTAAAATGGAAGTGCAAGAAGGAGGATGAGTCAAA AATCAGTGTTTCATGAGGCTCTCTTTTCAGCTGAAATGGAAGTGCAAGAAGGAGGATGAGTCAAA T C DNAJC17 Ensembl:ENSG00000104129 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:40775046..40775296 26863196 MeRIP-seq:(Medium) rs1176972965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1585314,Human_Splice_Rec_1585315,Human_Splice_Rec_1585322,Human_Splice_Rec_1585323,Human_Splice_Rec_1585344,Human_Splice_Rec_1585345,Human_Splice_Rec_1585366,Human_Splice_Rec_1585367,Human_Splice_Rec_1585382,Human_Splice_Rec_1585383,Human_Splice_Rec_1585398,Human_Splice_Rec_1585414,Human_Splice_Rec_1585415 RMVar_hsa_circ_10741,RMVar_hsa_circ_170953,RMVar_hsa_circ_102200,RMVar_hsa_circ_108598,RMVar_hsa_circ_170954,RMVar_hsa_circ_279175,RMVar_hsa_circ_322385,RMVar_hsa_circ_324364,RMVar_hsa_circ_125059,RMVar_hsa_circ_170957,RMVar_hsa_circ_170958,RMVar_hsa_circ_170959,RMVar_hsa_circ_170956 61767 RMVar_ID_61767 Human_SNP_ID_574524091 m1A Human chr15 + 40776291 40776291 40776291 GCTGCCGGGAACCCTCTTCTCTCAGGCGTTCGATCTGCAGAGCAGGGGGTGGGGGTGACAATTCT GCTGCCGGGAACCCTCTTCTCTCAGGCGTTCGCTCTGCAGAGCAGGGGGTGGGGGTGACAATTCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40776176..40776330 26863196 MeRIP-seq:(Medium) rs1380336499 Functional Loss SNV dbSNP153 33..33 33 - - - 61768 RMVar_ID_61768 Human_SNP_ID_574524172 m1A Human chr15 - 40776495 40776495 40776495 ACACTGGCCAGAAGGCCACCTGCAGGAGGAGGAGGTGGGGGAGGATGGACCTGGTGGTCGCCGTG ACACTGGCCAGAAGGCCACCTGCAGGAGGAGGCGGTGGGGGAGGATGGACCTGGTGGTCGCCGTG T G DNAJC17 Ensembl:ENSG00000104129 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40776493..40776650 26863196 MeRIP-seq:(Medium) rs747813426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170953,RMVar_hsa_circ_102200,RMVar_hsa_circ_108598,RMVar_hsa_circ_170954,RMVar_hsa_circ_279175,RMVar_hsa_circ_322385,RMVar_hsa_circ_324364,RMVar_hsa_circ_125059,RMVar_hsa_circ_170957,RMVar_hsa_circ_170958,RMVar_hsa_circ_170959,RMVar_hsa_circ_170956 61769 RMVar_ID_61769 Human_SNP_ID_574524866 m1A Human chr15 + 40779155 40779155 40779155 GCTTTGAGATGAGTTGCTGGAAGTGAAGCTTCAGGTGAGGGAGATGAATGAAAATGACCACAGGA GCTTTGAGATGAGTTGCTGGAAGTGAAGCTTCGGGTGAGGGAGATGAATGAAAATGACCACAGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40779153..40780129 26863196 MeRIP-seq:(Medium) rs771540868 Functional Loss SNV dbSNP153 33..33 33 - - - 61770 RMVar_ID_61770 Human_SNP_ID_574527268 m1A Human chr15 - 40789449 40789447 40789449 AAGGGAGGAGGTGGGCCAGAGAGCAGGGTGGTATCTGAGGAGGAGAAAGAGGGCTGTAGACTGGG AAGGGAGGAGGTGGGCCAGAGAGCAGGGTGGT__CTGAGGAGGAGAAAGAGGGCTGTAGACTGGG GAT G DNAJC17 Ensembl:ENSG00000104129 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40789234..40789583 26863196 MeRIP-seq:(Medium) rs1178603937 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12499678 RMVar_hsa_circ_125059,RMVar_hsa_circ_170959 61771 RMVar_ID_61771 Human_SNP_ID_574527269 m1A Human chr15 - 40789449 40789449 40789449 AAGGGAGGAGGTGGGCCAGAGAGCAGGGTGGTATCTGAGGAGGAGAAAGAGGGCTGTAGACTGGG AAGGGAGGAGGTGGGCCAGAGAGCAGGGTGGTTTCTGAGGAGGAGAAAGAGGGCTGTAGACTGGG T A DNAJC17 Ensembl:ENSG00000104129 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40789234..40789583 26863196 MeRIP-seq:(Medium) rs1437225476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12499678 RMVar_hsa_circ_125059,RMVar_hsa_circ_170959 61772 RMVar_ID_61772 Human_SNP_ID_574531948 m1A Human chr15 - 40807419 40807419 40807419 GAACCATGGCAGTGACCAAGGAGCTCTTACAGATGGACCTGTACGCGCTGCTAGGCATTGAGGAG GAACCATGGCAGTGACCAAGGAGCTCTTACAGGTGGACCTGTACGCGCTGCTAGGCATTGAGGAG T C DNAJC17 Ensembl:ENSG00000104129 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40807351..40807475 26863196 MeRIP-seq:(Medium) rs764077015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12499881 Human_Splice_Rec_1585301,Human_Splice_Rec_1585329,Human_Splice_Rec_1585353,Human_Splice_Rec_1585371,Human_Splice_Rec_1585385,Human_Splice_Rec_1585401,Human_Splice_Rec_1585417,Human_Splice_Rec_1585433 Human_miRNA_ID_2650270,Human_miRNA_ID_2756802 RMVar_hsa_circ_125059,RMVar_hsa_circ_170959 61773 RMVar_ID_61773 Human_SNP_ID_574531950 m1A Human chr15 - 40807421 40807421 40807421 CGGAACCATGGCAGTGACCAAGGAGCTCTTACAGATGGACCTGTACGCGCTGCTAGGCATTGAGG CGGAACCATGGCAGTGACCAAGGAGCTCTTACCGATGGACCTGTACGCGCTGCTAGGCATTGAGG T G DNAJC17 Ensembl:ENSG00000104129 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40807302..40807432 26863196 MeRIP-seq:(Medium) rs1345897739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12499881 Human_Splice_Rec_1585301,Human_Splice_Rec_1585329,Human_Splice_Rec_1585353,Human_Splice_Rec_1585371,Human_Splice_Rec_1585385,Human_Splice_Rec_1585401,Human_Splice_Rec_1585417,Human_Splice_Rec_1585433 Human_miRNA_ID_2756802 RMVar_hsa_circ_125059,RMVar_hsa_circ_170959 61774 RMVar_ID_61774 Human_SNP_ID_574532127 m1A Human chr15 + 40807752 40807752 40807752 GAAGGGAAGGGCGGAGCTGGGGTGAGGGTCCAAGGGGCCCAGGACTTGGCCGGCGTGATCTCAGC GAAGGGAAGGGCGGAGCTGGGGTGAGGGTCCAGGGGGCCCAGGACTTGGCCGGCGTGATCTCAGC A G ZFYVE19 Ensembl:ENSG00000166140 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:40807597..40807866;chr15:40807299..40807875 26863196 MeRIP-seq:(Medium) rs370613030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884156,Human_RBP_ID_3946157,Human_RBP_ID_4342582,Human_RBP_ID_5141255,Human_RBP_ID_8941182,Human_RBP_ID_9324489,Human_RBP_ID_9418423,Human_RBP_ID_18418336,Human_RBP_ID_22048186,Human_RBP_ID_26768761,Human_RBP_ID_26778864 Human_Splice_Rec_1585591 61775 RMVar_ID_61775 Human_SNP_ID_574532585 m1A Human chr15 - 40809149 40809149 40809149 CACTGCTGCACTGAAGCTTAGGCAGCCTGAACAGAAGGCCCTGCCACAATTCTTACAGCCGTACT CACTGCTGCACTGAAGCTTAGGCAGCCTGAACGGAAGGCCCTGCCACAATTCTTACAGCCGTACT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40809047..40809148 32194978 MeRIP-seq:(Medium) rs17851856 Functional Loss SNV dbSNP153 33..33 33 - - - 61776 RMVar_ID_61776 Human_SNP_ID_574549753 m1A Human chr15 + 40872573 40872573 40872573 CCAGGCCTTATCCACCATCAGTCCCAGGCTCCAAGACCTCTTTTCCTGCTCGCTCTCTCAATCTC CCAGGCCTTATCCACCATCAGTCCCAGGCTCCGAGACCTCTTTTCCTGCTCGCTCTCTCAATCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:40872305..40872730;chr15:40872201..40872920 26863196 MeRIP-seq:(Medium) rs917922339 Functional Loss SNV dbSNP153 33..33 33 - - - 61777 RMVar_ID_61777 Human_SNP_ID_574555292 m1A Human chr15 - 40894513 40894513 40894513 TTGCACCTTACTCCCCGCCCCCGCTACAAAAAAATCACAGGCTCCCTTCAGCCGGTGCCAGGTGA TTGCACCTTACTCCCCGCCCCCGCTACAAAAAGATCACAGGCTCCCTTCAGCCGGTGCCAGGTGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40894463..40894780 26863196 MeRIP-seq:(Medium) rs1048984734 Functional Loss SNV dbSNP153 33..33 33 - - - 61778 RMVar_ID_61778 Human_SNP_ID_574555293 m1A Human chr15 - 40894513 40894513 40894513 TTGCACCTTACTCCCCGCCCCCGCTACAAAAAAATCACAGGCTCCCTTCAGCCGGTGCCAGGTGA TTGCACCTTACTCCCCGCCCCCGCTACAAAAACATCACAGGCTCCCTTCAGCCGGTGCCAGGTGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40894463..40894780 26863196 MeRIP-seq:(Medium) rs1048984734 Functional Loss SNV dbSNP153 33..33 33 - - - 61779 RMVar_ID_61779 Human_SNP_ID_574585979 m1A Human chr15 + 40995898 40995898 40995898 CTGACAGCCCTCCCATAGTATGACAGATGCTGATGATGTACAGCTACCCAGCAATGCCTCCAGTG CTGACAGCCCTCCCATAGTATGACAGATGCTGCTGATGTACAGCTACCCAGCAATGCCTCCAGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40995895..40995992 26863196 MeRIP-seq:(Medium) rs1397369824 Functional Loss SNV dbSNP153 33..33 33 - - - 61780 RMVar_ID_61780 Human_SNP_ID_574618714 m1A Human chr15 - 41115516 41115516 41115516 ACAAATGAGATCTAAGGGCTTGTTAGTGTGTCATTTTGTAAGGGGCAAGTTGAGATACGGTTGAA ACAAATGAGATCTAAGGGCTTGTTAGTGTGTCTTTTTGTAAGGGGCAAGTTGAGATACGGTTGAA T A INO80 Ensembl:ENSG00000128908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41115477..41115732 26863196 MeRIP-seq:(Medium) rs890295420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12501691 RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 61781 RMVar_ID_61781 Human_SNP_ID_574618945 m1A Human chr15 - 41116103 41116103 41116103 GGGAGCGAGCTAGGAGCGTCCACGCCCAACGCAGTCACCGTCCCACGGCCTCAGAGAGCGAACCG GGGAGCGAGCTAGGAGCGTCCACGCCCAACGCTGTCACCGTCCCACGGCCTCAGAGAGCGAACCG T A INO80 Ensembl:ENSG00000128908 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:41116041..41116211;chr15:41116053..41116230 26863196 MeRIP-seq:(Medium) rs974641182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2037603,Human_miRNA_ID_2348304 RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 61782 RMVar_ID_61782 Human_SNP_ID_574618959 m1A Human chr15 - 41116147 41116147 41116147 CCGCCTCAGCGCCGCCGCCATCTTGGGGTCCCAGGAGCCGCGGAGGGAGCGAGCTAGGAGCGTCC CCGCCTCAGCGCCGCCGCCATCTTGGGGTCCCCGGAGCCGCGGAGGGAGCGAGCTAGGAGCGTCC T G INO80 Ensembl:ENSG00000128908 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:41116069..41116248 26863196 MeRIP-seq:(Medium) rs1396494195 Functional Loss SNV dbSNP153 33..33 33 - - - 61783 RMVar_ID_61783 Human_SNP_ID_574650017 m1A Human chr15 + 41231302 41231302 41231302 TGGAAACACTGCCCTCTCCCTTCTTGACCCCTAGCCCTTCCTTCCCTCCCTCCTTCCCTCCTGTC TGGAAACACTGCCCTCTCCCTTCTTGACCCCTGGCCCTTCCTTCCCTCCCTCCTTCCCTCCTGTC A G CHP1 Ensembl:ENSG00000187446 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr15:41231251..41231450 26863196 MeRIP-seq:(Medium) rs1422311856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343039,Human_RBP_ID_5418544,Human_RBP_ID_5439617,Human_RBP_ID_5495032,Human_RBP_ID_18937732,Human_RBP_ID_27434872 61784 RMVar_ID_61784 Human_SNP_ID_574663479 m1A Human chr15 + 41284046 41284046 41284046 CGAAGATGGCGGAGTAAGGCGTGCCGCTGCAAACTGGCCTCTGGGCCGGGGGCGAGCAGCCCCCG CGAAGATGGCGGAGTAAGGCGTGCCGCTGCAAGCTGGCCTCTGGGCCGGGGGCGAGCAGCCCCCG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:41284001..41284150 26863196 MeRIP-seq:(Medium) rs969132770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232881,Human_RBP_ID_456829,Human_RBP_ID_759970,Human_RBP_ID_814493,Human_RBP_ID_886344,Human_RBP_ID_1511792,Human_RBP_ID_3490394,Human_RBP_ID_4342242,Human_RBP_ID_5087790,Human_RBP_ID_5180444,Human_RBP_ID_6423707,Human_RBP_ID_9370733,Human_RBP_ID_18418337,Human_RBP_ID_22934711,Human_RBP_ID_26326522,Human_RBP_ID_27809350 Human_Splice_Rec_1586361,Human_Splice_Rec_1586371,Human_Splice_Rec_1586377,Human_Splice_Rec_1586383,Human_Splice_Rec_1586389,Human_Splice_Rec_1586397,Human_Splice_Rec_1586399,Human_Splice_Rec_1586405,Human_Splice_Rec_1586411,Human_Splice_Rec_1586419,Human_Splice_Rec_1586447 61785 RMVar_ID_61785 Human_SNP_ID_574663509 m1A Human chr15 - 41284097 41284097 41284097 ACTGGCCTTCTCGGCTCACCTCGCACGGTCCAACAGATGCACTCGGCCTCCCGGGGGCTGCTCGC ACTGGCCTTCTCGGCTCACCTCGCACGGTCCAGCAGATGCACTCGGCCTCCCGGGGGCTGCTCGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:41284001..41284151 26863196 MeRIP-seq:(Medium) rs896895014 Functional Loss SNV dbSNP153 33..33 33 - - - 61786 RMVar_ID_61786 Human_SNP_ID_574663803 m1A Human chr15 + 41285166 41285166 41285166 GCTGAAAAATAATACAGAAGGACTTTTATATGAGACCTTTTTTGTCGCTCTGTCAGTTTATTTTT GCTGAAAAATAATACAGAAGGACTTTTATATGTGACCTTTTTTGTCGCTCTGTCAGTTTATTTTT A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:41285164..41285350 26863196 MeRIP-seq:(Medium) rs942147892 Functional Loss SNV dbSNP153 33..33 33 - - - 61787 RMVar_ID_61787 Human_SNP_ID_574663820 m1A Human chr15 + 41285231 41285230 41285231 TGTTTTTTTGTCTTTGTCTCATCCAGGAGAAGAAAAAAAATATCGGCCAGAGGAGAGGAACTAAC TGTTTTTTTGTCTTTGTCTCATCCAGGAGAAG_AAAAAAATATCGGCCAGAGGAGAGGAACTAAC GA G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:41285226..41285275 26863410 MeRIP-seq:(Medium) rs1230954315 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_886346,Human_RBP_ID_1511667,Human_RBP_ID_4342590,Human_RBP_ID_5180484,Human_RBP_ID_5568898,Human_RBP_ID_5646575,Human_RBP_ID_8183611,Human_RBP_ID_9345360,Human_RBP_ID_9370735,Human_RBP_ID_17859854,Human_RBP_ID_22048091,Human_RBP_ID_22540800,Human_RBP_ID_25183695,Human_RBP_ID_26326525,Human_RBP_ID_26808819,Human_RBP_ID_27809351 Human_Splice_Rec_1586362,Human_Splice_Rec_1586366,Human_Splice_Rec_1586372,Human_Splice_Rec_1586378,Human_Splice_Rec_1586384,Human_Splice_Rec_1586390,Human_Splice_Rec_1586398,Human_Splice_Rec_1586400,Human_Splice_Rec_1586406,Human_Splice_Rec_1586412,Human_Splice_Rec_1586420,Human_Splice_Rec_1586448 Human_miRNA_ID_2364488,Human_miRNA_ID_2364489 RMVar_hsa_circ_121853,RMVar_hsa_circ_171045,RMVar_hsa_circ_118405,RMVar_hsa_circ_171044 61788 RMVar_ID_61788 Human_SNP_ID_574676807 m1A Human chr15 + 41332452 41332452 41332452 AGGACCCCTTCACCACCTGCGTATCCCACTCCATGGAGGTCGTAAAAGAAGCTTGGTCAATCGCC AGGACCCCTTCACCACCTGCGTATCCCACTCCGTGGAGGTCGTAAAAGAAGCTTGGTCAATCGCC A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41332401..41332575 26863196 MeRIP-seq:(Medium) rs560529830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17859960 61789 RMVar_ID_61789 Human_SNP_ID_574676808 m1A Human chr15 + 41332452 41332452 41332452 AGGACCCCTTCACCACCTGCGTATCCCACTCCATGGAGGTCGTAAAAGAAGCTTGGTCAATCGCC AGGACCCCTTCACCACCTGCGTATCCCACTCCTTGGAGGTCGTAAAAGAAGCTTGGTCAATCGCC A T NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41332401..41332575 26863196 MeRIP-seq:(Medium) rs560529830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17859960 61790 RMVar_ID_61790 Human_SNP_ID_574676864 m1A Human chr15 - 41332532 41332532 41332532 AAGATGGCGGCTCAGCCGCTGCGGCATCGCTCACGTTGTGCAACGCCGCCCCGGGGGGACTTTTG AAGATGGCGGCTCAGCCGCTGCGGCATCGCTCGCGTTGTGCAACGCCGCCCCGGGGGGACTTTTG T C OIP5 Ensembl:ENSG00000104147 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:41332365..41332600;chr15:41332351..41332600 26863196 MeRIP-seq:(Medium) rs755047401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342591 RMVar_hsa_circ_171048,RMVar_hsa_circ_95181 61791 RMVar_ID_61791 Human_SNP_ID_574677080 m1A Human chr15 + 41332925 41332925 41332925 ATTTGAACCGCGCTGACGAAGTTTGGTGATCCATCTTCCGAGTATCGCCGGGATTTCGAATCGCG ATTTGAACCGCGCTGACGAAGTTTGGTGATCCGTCTTCCGAGTATCGCCGGGATTTCGAATCGCG A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41332876..41332925 26863196 MeRIP-seq:(Medium) rs1254515260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457015,Human_RBP_ID_1174432,Human_RBP_ID_1504373,Human_RBP_ID_4320658,Human_RBP_ID_5464590,Human_RBP_ID_5494340,Human_RBP_ID_8416201,Human_RBP_ID_9324229,Human_RBP_ID_18662246,Human_RBP_ID_22047409,Human_RBP_ID_26930989 Human_Splice_Rec_1586529 RMVar_hsa_circ_99120,RMVar_hsa_circ_171049 61792 RMVar_ID_61792 Human_SNP_ID_574677086 m1A Human chr15 + 41332933 41332933 41332933 CGCGCTGACGAAGTTTGGTGATCCATCTTCCGAGTATCGCCGGGATTTCGAATCGCGATGATCAT CGCGCTGACGAAGTTTGGTGATCCATCTTCCGGGTATCGCCGGGATTTCGAATCGCGATGATCAT A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:41332876..41333088;chr15:41332876..41333002 26863196 MeRIP-seq:(Medium) rs1179644405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1174432,Human_RBP_ID_1504373,Human_RBP_ID_4320658,Human_RBP_ID_5464590,Human_RBP_ID_5494340,Human_RBP_ID_8416201,Human_RBP_ID_9324229,Human_RBP_ID_18662246,Human_RBP_ID_22047409,Human_RBP_ID_26930989 Human_Splice_Rec_1586529 RMVar_hsa_circ_99120,RMVar_hsa_circ_171049 61793 RMVar_ID_61793 Human_SNP_ID_574681522 m1A Human chr15 - 41349187 41349187 41349187 ACAGTCTTGCACCTTCTCCTTGTTTTGGTGACATGGCCAAGTGGCTGTCTCTCAGCTTCTTCCTG ACAGTCTTGCACCTTCTCCTTGTTTTGGTGACTTGGCCAAGTGGCTGTCTCTCAGCTTCTTCCTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:41349136..41349271 26863196 MeRIP-seq:(Medium) rs778005789 Functional Loss SNV dbSNP153 33..33 33 - - - 61794 RMVar_ID_61794 Human_SNP_ID_574689800 m1A Human chr15 - 41380222 41380221 41380222 AAAAAAAAAAATTTACAAAAGGAAAAAAGTTGAGAATACAGGAATATTTACAAGATGTTAAAAAA AAAAAAAAAAATTTACAAAAGGAAAAAAGTTG_GAATACAGGAATATTTACAAGATGTTAAAAAA CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:41380076..41380300 32194978 MeRIP-seq:(Medium) rs758066976 Functional Loss DEL dbSNP153 33..33 33 - - - 61795 RMVar_ID_61795 Human_SNP_ID_574697067 m1A Human chr15 + 41402409 41402409 41402409 CCTCAAGTGCCAGGGCTCTGTCGCCTCCCCACACCCGGGACACACCAACCGCCGGCCTGCCGCCG CCTCAAGTGCCAGGGCTCTGTCGCCTCCCCACTCCCGGGACACACCAACCGCCGGCCTGCCGCCG A T OIP5-AS1 RNACentral:URS0000D5D5A0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41402191..41402450 26863196 MeRIP-seq:(Medium) rs1307931620 Functional Loss SNV dbSNP153 33..33 33 - - - 61796 RMVar_ID_61796 Human_SNP_ID_574700954 m1A Human chr15 + 41417175 41417175 41417175 GCAGCGGCGGCGGCGGCGGCAGTGGCGGTCCCACTGGCAGGCGGGCAAGAGGGGAGTCCGGGCGG GCAGCGGCGGCGGCGGCGGCAGTGGCGGTCCCGCTGGCAGGCGGGCAAGAGGGGAGTCCGGGCGG A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr15:41417130..41417291;chr15:41417125..41417300 26863196 MeRIP-seq:(Medium) rs1289560800 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_43139,Human_RBP_ID_4342596,Human_RBP_ID_8804050,Human_RBP_ID_9324490,Human_RBP_ID_18418339,Human_RBP_ID_26327360,Human_RBP_ID_27809357 61797 RMVar_ID_61797 Human_SNP_ID_574700964 m1A Human chr15 + 41417189 41417189 41417189 GGCGGCAGTGGCGGTCCCACTGGCAGGCGGGCAAGAGGGGAGTCCGGGCGGCGGCCGGCGTGGGA GGCGGCAGTGGCGGTCCCACTGGCAGGCGGGCGAGAGGGGAGTCCGGGCGGCGGCCGGCGTGGGA A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:41417125..41417341 26863196 MeRIP-seq:(Medium) rs777836965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43139,Human_RBP_ID_4320783,Human_RBP_ID_8804050,Human_RBP_ID_9324490,Human_RBP_ID_9370750,Human_RBP_ID_18418339,Human_RBP_ID_26326537,Human_RBP_ID_27809357 61798 RMVar_ID_61798 Human_SNP_ID_574700990 m1A Human chr15 + 41417253 41417253 41417253 AGCCGGGGGACCACCATGGTAAAGAAGCGGAAAGGCCGCGTCGTGATCGACTCGGACACAGAGGA AGCCGGGGGACCACCATGGTAAAGAAGCGGAAGGGCCGCGTCGTGATCGACTCGGACACAGAGGA A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:41417134..41417300 26863196 MeRIP-seq:(Medium) rs1210479028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759955,Human_RBP_ID_4342596,Human_RBP_ID_5566307,Human_RBP_ID_8804051,Human_RBP_ID_9370750,Human_RBP_ID_18418339,Human_RBP_ID_26326318,Human_RBP_ID_27810112 Human_Splice_Rec_1586735,Human_Splice_Rec_1586767 61799 RMVar_ID_61799 Human_SNP_ID_574703494 m1A Human chr15 - 41426725 41426725 41426725 TAGACTCACGCCTGTAATCCCAACACTTCAGGAGGCCGGCGGGGGGGGGGGGCGGGGGGGGGGGG TAGACTCACGCCTGTAATCCCAACACTTCAGGGGGCCGGCGGGGGGGGGGGGCGGGGGGGGGGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:41426676..41426811 26863196 MeRIP-seq:(Medium) rs1449461462 Functional Loss SNV dbSNP153 33..33 33 - - - 61800 RMVar_ID_61800 Human_SNP_ID_574710671 m1A Human chr15 - 41452863 41452863 41452863 AGGAGAAAAGAAAAAGGAAGACTGAAATAGGAATAGGGACTTTATTGGGAAAAGCTGGAAGACTC AGGAGAAAAGAAAAAGGAAGACTGAAATAGGAGTAGGGACTTTATTGGGAAAAGCTGGAAGACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41452860..41453006 26863196 MeRIP-seq:(Medium) rs755728450 Functional Loss SNV dbSNP153 33..33 33 - - - 61801 RMVar_ID_61801 Human_SNP_ID_574710692 m1A Human chr15 - 41452950 41452950 41452950 TGGCCTGTTTCTTCATGGTTCCTTTCTTCTCTATTTTTCTGGCTTTTCCTTTCTTCTTATTTTTA TGGCCTGTTTCTTCATGGTTCCTTTCTTCTCTGTTTTTCTGGCTTTTCCTTTCTTCTTATTTTTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41452844..41453025 26863196 MeRIP-seq:(Medium) rs747208093 Functional Loss SNV dbSNP153 33..33 33 - - - 61802 RMVar_ID_61802 Human_SNP_ID_574721460 m1A Human chr15 - 41493922 41493922 41493922 GCCCGTTGGGCCCCCGGGCAGGGTCATTTCCCAGTGCCGGCGCCGCCGCTGAGCCCACCAGCCCG GCCCGTTGGGCCCCCGGGCAGGGTCATTTCCCGGTGCCGGCGCCGCCGCTGAGCCCACCAGCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:41493874..41494020 26863196 MeRIP-seq:(Medium) rs1001374657 Functional Loss SNV dbSNP153 33..33 33 - - - 61803 RMVar_ID_61803 Human_SNP_ID_574730989 m1A Human chr15 + 41522949 41522949 41522949 GGGCTGGCACACAGGACAGCGGGTTGCAGAGAAGGGAGCAGTGCCTGTAGGTGAAGTGGAGAGTC GGGCTGGCACACAGGACAGCGGGTTGCAGAGAGGGGAGCAGTGCCTGTAGGTGAAGTGGAGAGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:41522898..41523282 32194978 MeRIP-seq:(Medium) rs1156893744 Functional Loss SNV dbSNP153 33..33 33 - - - 61804 RMVar_ID_61804 Human_SNP_ID_574735363 m1A Human chr15 + 41537194 41537194 41537194 CCAGCAGTGTCTCCGTGTGGGGGTTCCCTCTTATTCATCCCTAAGAGCAAGAAAGAATATGGGCC CCAGCAGTGTCTCCGTGTGGGGGTTCCCTCTTTTTCATCCCTAAGAGCAAGAAAGAATATGGGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41537015..41543919 26863196 MeRIP-seq:(Medium) rs1254121653 Functional Loss SNV dbSNP153 33..33 33 - - - 61805 RMVar_ID_61805 Human_SNP_ID_574737014 m1A Human chr15 + 41544150 41544150 41544150 CCAAAGGCCCGCAGGCAGGTTCCAGCAAAGAAACTGGACACGCTACCCTGGGTCCTCCTCCCAGA CCAAAGGCCCGCAGGCAGGTTCCAGCAAAGAAGCTGGACACGCTACCCTGGGTCCTCCTCCCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41544141..41544236 26863196 MeRIP-seq:(Medium) rs1303373454 Functional Loss SNV dbSNP153 33..33 33 - - - 61806 RMVar_ID_61806 Human_SNP_ID_574741199 m1A Human chr15 + 41559060 41559060 41559060 AGGAGCGCGGTGGCGCGGGAGCGGCCCCGGGGACCCCGCGCTGCTGACGGCGGCGACCGCGGCCG AGGAGCGCGGTGGCGCGGGAGCGGCCCCGGGGTCCCCGCGCTGCTGACGGCGGCGACCGCGGCCG A T TYRO3 Ensembl:ENSG00000092445 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41558945..41559148 26863196 MeRIP-seq:(Medium) rs956796688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342249 RMVar_hsa_circ_124495,RMVar_hsa_circ_171098,RMVar_hsa_circ_94029,RMVar_hsa_circ_171097 61807 RMVar_ID_61807 Human_SNP_ID_574741291 m1A Human chr15 - 41559292 41559292 41559292 GCCGCGGTGGCGGCGGCAGCGGCAGCGGCGGGAGCCCCGGCCGCCCCATGCTCCGCCTCAGCGCC GCCGCGGTGGCGGCGGCAGCGGCAGCGGCGGGGGCCCCGGCCGCCCCATGCTCCGCCTCAGCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41559249..41559330 26863196 MeRIP-seq:(Medium) rs1005142711 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 61808 RMVar_ID_61808 Human_SNP_ID_574741293 m1A Human chr15 - 41559301 41559295 41559301 GCAGCCCGAGCCGCGGTGGCGGCGGCAGCGGCAGCGGCGGGAGCCCCGGCCGCCCCATGCTCCGC GCAGCCCGAGCCGCGGTGGCGGCGGCAGCGGC______GGGAGCCCCGGCCGCCCCATGCTCCGC CGCCGCT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:41559117..41559313 26863410 MeRIP-seq:(Medium) rs534867062 Functional Loss DEL dbSNP153 33..38 33 - - - 61809 RMVar_ID_61809 Human_SNP_ID_574741298 m1A Human chr15 - 41559301 41559301 41559301 GCAGCCCGAGCCGCGGTGGCGGCGGCAGCGGCAGCGGCGGGAGCCCCGGCCGCCCCATGCTCCGC GCAGCCCGAGCCGCGGTGGCGGCGGCAGCGGCGGCGGCGGGAGCCCCGGCCGCCCCATGCTCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:41559117..41559313 26863410 MeRIP-seq:(Medium) rs1220758670 Functional Loss SNV dbSNP153 33..33 33 - - - 61810 RMVar_ID_61810 Human_SNP_ID_574741937 m1A Human chr15 + 41561220 41561220 41561220 CAACTGCAGTGTGGAGGGGATGGAGGAGCCTGACATCCAGTGGGTGAAGGATGGGGCTGTGGTCC CAACTGCAGTGTGGAGGGGATGGAGGAGCCTGGCATCCAGTGGGTGAAGGATGGGGCTGTGGTCC A G TYRO3 Ensembl:ENSG00000092445 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:41559284..41561230 32194978 MeRIP-seq:(Medium) rs1391906779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343049 Human_Splice_Rec_1587199,Human_Splice_Rec_1587234,Human_Splice_Rec_1587235,Human_Splice_Rec_1587270 RMVar_hsa_circ_124495,RMVar_hsa_circ_171098,RMVar_hsa_circ_94029,RMVar_hsa_circ_171097 61811 RMVar_ID_61811 Human_SNP_ID_574761544 m1A Human chr15 - 41634963 41634924 41634963 CATCCTAATAATCTCCTAAGTGTTCTTACTTCAAACTATTCTCATCACCACTGCAAAATCAAATA CATCCTAATAATCTCCTAAGTGTTCTTACTTC_________________________________ GGAAAAATATTTGATTTTGCAGTGGTGATGAGAATAGTTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41634959..41635098 26863196 MeRIP-seq:(Medium) rs1315398107 Functional Loss DEL dbSNP153 33..65 33 - - - 61812 RMVar_ID_61812 Human_SNP_ID_574762068 m1A Human chr15 + 41637061 41637060 41637061 GCTCTGGGGGCGGGGGTGGTAAAGGTCGTAGTAAAGAGAGAAATGTGAGAAAATACTTGAAGGAG GCTCTGGGGGCGGGGGTGGTAAAGGTCGTAGT_AAGAGAGAAATGTGAGAAAATACTTGAAGGAG TA T MGA Ensembl:ENSG00000174197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41637047..41637182 26863196 MeRIP-seq:(Medium) rs1266927019 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103369,RMVar_hsa_circ_171106 61813 RMVar_ID_61813 Human_SNP_ID_574762069 m1A Human chr15 + 41637061 41637061 41637061 GCTCTGGGGGCGGGGGTGGTAAAGGTCGTAGTAAAGAGAGAAATGTGAGAAAATACTTGAAGGAG GCTCTGGGGGCGGGGGTGGTAAAGGTCGTAGTGAAGAGAGAAATGTGAGAAAATACTTGAAGGAG A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41637047..41637182 26863196 MeRIP-seq:(Medium) rs1050833825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103369,RMVar_hsa_circ_171106 61814 RMVar_ID_61814 Human_SNP_ID_574782980 m1A Human chr15 + 41713456 41713456 41713456 GAGGAGGAAGAAGGAATCAGGGAGGAGGAGGAACAATTGAAAGAGAAAAAGAAGAGAAAGAAGCT GAGGAGGAAGAAGGAATCAGGGAGGAGGAGGAGCAATTGAAAGAGAAAAAGAAGAGAAAGAAGCT A G MGA Ensembl:ENSG00000174197 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41713406..41713472 26863196 MeRIP-seq:(Medium) rs772143722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42745,Human_RBP_ID_884170,Human_RBP_ID_2440161,Human_RBP_ID_4344818,Human_RBP_ID_6424749,Human_RBP_ID_17651931,Human_RBP_ID_17860071,Human_RBP_ID_18278860,Human_RBP_ID_22928555,Human_RBP_ID_24544204,Human_RBP_ID_26326557,Human_RBP_ID_27434977,Human_RBP_ID_27809375 Human_Splice_Rec_1587419,Human_Splice_Rec_1587463,Human_Splice_Rec_1587507,Human_Splice_Rec_1587549 Human_miRNA_ID_1132762 RMVar_hsa_circ_62516,RMVar_hsa_circ_361602,RMVar_hsa_circ_362942,RMVar_hsa_circ_293603,RMVar_hsa_circ_99996,RMVar_hsa_circ_63725,RMVar_hsa_circ_171110,RMVar_hsa_circ_28966,RMVar_hsa_circ_61298,RMVar_hsa_circ_321059,RMVar_hsa_circ_171108,RMVar_hsa_circ_171109,RMVar_hsa_circ_361195,RMVar_hsa_circ_328073,RMVar_hsa_circ_319720,RMVar_hsa_circ_109765,RMVar_hsa_circ_267209,RMVar_hsa_circ_272944,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_171116,RMVar_hsa_circ_171120,RMVar_hsa_circ_171121,RMVar_hsa_circ_171118,RMVar_hsa_circ_171119,RMVar_hsa_circ_171117,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_126451,RMVar_hsa_circ_84,RMVar_hsa_circ_171125,RMVar_hsa_circ_322292,RMVar_hsa_circ_68198,RMVar_hsa_circ_286685,RMVar_hsa_circ_17990,RMVar_hsa_circ_50622,RMVar_hsa_circ_171127,RMVar_hsa_circ_171128,RMVar_hsa_circ_358555,RMVar_hsa_circ_368129,RMVar_hsa_circ_375598,RMVar_hsa_circ_364918,RMVar_hsa_circ_57489,RMVar_hsa_circ_171129 61815 RMVar_ID_61815 Human_SNP_ID_574795053 m1A Human chr15 + 41759065 41759065 41759065 GGTGAGAGAGGGAAGAAGAAATAAAGGGAAGGATACAGGTGCTGATACCCTCATTTTACAAAGTA GGTGAGAGAGGGAAGAAGAAATAAAGGGAAGGGTACAGGTGCTGATACCCTCATTTTACAAAGTA A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41759047..41759187 26863196 MeRIP-seq:(Medium) rs1259773471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232347,Human_RBP_ID_23651139 RMVar_hsa_circ_631,RMVar_hsa_circ_61298,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_64804,RMVar_hsa_circ_98042,RMVar_hsa_circ_171138,RMVar_hsa_circ_30975,RMVar_hsa_circ_343003,RMVar_hsa_circ_274463,RMVar_hsa_circ_339736,RMVar_hsa_circ_321875,RMVar_hsa_circ_301549,RMVar_hsa_circ_171146,RMVar_hsa_circ_171147,RMVar_hsa_circ_171148,RMVar_hsa_circ_359928,RMVar_hsa_circ_314261 61816 RMVar_ID_61816 Human_SNP_ID_574799477 m1A Human chr15 - 41774565 41774565 41774565 CTAAGGCCACCCCGCTCACAGCGCCCTCGGGCATCGCGTTCGGCAATTTCAGCTCCGCCGCGGTA CTAAGGCCACCCCGCTCACAGCGCCCTCGGGCGTCGCGTTCGGCAATTTCAGCTCCGCCGCGGTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41774517..41774715 26863196 MeRIP-seq:(Medium) rs1393354063 Functional Loss SNV dbSNP153 33..33 33 - - - 61817 RMVar_ID_61817 Human_SNP_ID_574799501 m1A Human chr15 - 41774612 41774612 41774612 ACTCGTCAGCGCCCCCGTTCGGGCCCAGCCTCACCAGCCTCGGCGAGCTAAGGCCACCCCGCTCA ACTCGTCAGCGCCCCCGTTCGGGCCCAGCCTCGCCAGCCTCGGCGAGCTAAGGCCACCCCGCTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:41774567..41774674 26863196 MeRIP-seq:(Medium) rs1301529923 Functional Loss SNV dbSNP153 33..33 33 - - - 61818 RMVar_ID_61818 Human_SNP_ID_574801414 m1A Human chr15 + 41782264 41782259 41782264 AGCCTGGGAGATAGCGAGGCTCTGTCTCAAAAAAAAAAAAAAAAAATTATGAAATACAACAGACA AGCCTGGGAGATAGCGAGGCTCTGTCTC_____AAAAAAAAAAAAATTATGAAATACAACAGACA CAAAAA C MAPKBP1 Ensembl:ENSG00000137802 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:41782186..41782276 26863410 MeRIP-seq:(Medium) rs10629541 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_99150,RMVar_hsa_circ_171150 61819 RMVar_ID_61819 Human_SNP_ID_574801415 m1A Human chr15 + 41782264 41782259 41782264 AGCCTGGGAGATAGCGAGGCTCTGTCTCAAAAAAAAAAAAAAAAAATTATGAAATACAACAGACA AGCCTGGGAGATAGCGAGGCTCTGTCTCAAA__AAAAAAAAAAAAATTATGAAATACAACAGACA CAAAAA CAAA MAPKBP1 Ensembl:ENSG00000137802 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:41782186..41782276 26863410 MeRIP-seq:(Medium) rs10629541 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_99150,RMVar_hsa_circ_171150 61820 RMVar_ID_61820 Human_SNP_ID_574801416 m1A Human chr15 + 41782264 41782259 41782264 AGCCTGGGAGATAGCGAGGCTCTGTCTCAAAAAAAAAAAAAAAAAATTATGAAATACAACAGACA AGCCTGGGAGATAGCGAGGCTCTGTCTCAAAA_AAAAAAAAAAAAATTATGAAATACAACAGACA CAAAAA CAAAA MAPKBP1 Ensembl:ENSG00000137802 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:41782186..41782276 26863410 MeRIP-seq:(Medium) rs10629541 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_99150,RMVar_hsa_circ_171150 61821 RMVar_ID_61821 Human_SNP_ID_574813510 m1A Human chr15 - 41826753 41826753 41826753 CATTCTAACTTATCCCCTCACCTCTGCCACTTACCTGTCCCATCTACCACTTTTCTAGTGTCTCC CATTCTAACTTATCCCCTCACCTCTGCCACTTCCCTGTCCCATCTACCACTTTTCTAGTGTCTCC T G AC020659.2 Ensembl:ENSG00000250379 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41826645..41826956 26863196 MeRIP-seq:(Medium) rs929788431 Functional Loss SNV dbSNP153 33..33 33 - - - 61822 RMVar_ID_61822 Human_SNP_ID_574813536 m1A Human chr15 + 41826847 41826847 41826847 AGGAGATAGGGGACCCTAGGAGGTAGAGTGGGACCATGTCGTGAGGCAGTTGAAGAGTTGAGGAA AGGAGATAGGGGACCCTAGGAGGTAGAGTGGGTCCATGTCGTGAGGCAGTTGAAGAGTTGAGGAA A T MAPKBP1 Ensembl:ENSG00000137802 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41826648..41826978 26863196 MeRIP-seq:(Medium) rs1347799124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12507216,Human_RBP_ID_23651241 61823 RMVar_ID_61823 Human_SNP_ID_574813702 m1A Human chr15 + 41827290 41827290 41827290 CCATTGCACTCCAACCTAGGTGACAAAGCTACACGCCATCTCAAAAAAAAAAAAGAAAAAGGGTT CCATTGCACTCCAACCTAGGTGACAAAGCTACGCGCCATCTCAAAAAAAAAAAAGAAAAAGGGTT A G MAPKBP1 Ensembl:ENSG00000137802 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:41827241..41827346 26863196 MeRIP-seq:(Medium) rs916281486 Functional Loss SNV dbSNP153 33..33 33 - - - 61824 RMVar_ID_61824 Human_SNP_ID_574821431 m1A Human chr15 + 41847419 41847419 41847419 ACCCATCTCGCCCAGCCCCGAAGAGCAGCTCCAGCCTCGGGAGTGCCACACCTTCTCCGACCCCA ACCCATCTCGCCCAGCCCCGAAGAGCAGCTCCGGCCTCGGGAGTGCCACACCTTCTCCGACCCCA A G JMJD7-PLA2G4B,PLA2G4B Ensembl:ENSG00000168970,Ensembl:ENSG00000243708 Protein coding,Protein coding exon,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:41847394..41847533 26863196 MeRIP-seq:(Medium) rs776135432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1588102,Human_Splice_Rec_1588148,Human_Splice_Rec_1588192,Human_Splice_Rec_1588280,Human_Splice_Rec_1588318,Human_Splice_Rec_1588370,Human_Splice_Rec_1588392 RMVar_hsa_circ_113092,RMVar_hsa_circ_116729,RMVar_hsa_circ_171155,RMVar_hsa_circ_171156 61825 RMVar_ID_61825 Human_SNP_ID_574824734 m1A Human chr15 - 41853719 41853719 41853719 CTACAGACGGAGGCCTGCCGACTGGGCCAGCTACATCCTGCAGCTCCGGGGGGCCTGGCCAAGGT CTACAGACGGAGGCCTGCCGACTGGGCCAGCTCCATCCTGCAGCTCCGGGGGGCCTGGCCAAGGT T G SPTBN5 Ensembl:ENSG00000137877 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41853694..41853760 26863196 MeRIP-seq:(Medium) rs1388226035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1588508 RMVar_hsa_circ_105544,RMVar_hsa_circ_171158 61826 RMVar_ID_61826 Human_SNP_ID_574826445 m1A Human chr15 + 41857403 41857403 41857403 TCTGTGTGCCCAGGAGCTCGCCCACCCCAGGCAGGGCCTGGCCCACAGTGGGGGCTCTCAGCTCA TCTGTGTGCCCAGGAGCTCGCCCACCCCAGGCGGGGCCTGGCCCACAGTGGGGGCTCTCAGCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41857352..41857430 26863196 MeRIP-seq:(Medium) rs574798174 Functional Loss SNV dbSNP153 33..33 33 - - - 61827 RMVar_ID_61827 Human_SNP_ID_574826446 m1A Human chr15 + 41857403 41857403 41857403 TCTGTGTGCCCAGGAGCTCGCCCACCCCAGGCAGGGCCTGGCCCACAGTGGGGGCTCTCAGCTCA TCTGTGTGCCCAGGAGCTCGCCCACCCCAGGCTGGGCCTGGCCCACAGTGGGGGCTCTCAGCTCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:41857352..41857430 26863196 MeRIP-seq:(Medium) rs574798174 Functional Loss SNV dbSNP153 33..33 33 - - - 61828 RMVar_ID_61828 Human_SNP_ID_574845337 m1A Human chr15 - 41919427 41919427 41919427 CCAAGTGGACACGCAGCAGCTGATGCGGGTCTACGGGGCCCTCATGTGGTCCCTAGGCAAGGTCA CCAAGTGGACACGCAGCAGCTGATGCGGGTCTGCGGGGCCCTCATGTGGTCCCTAGGCAAGGTCA T C EHD4 Ensembl:ENSG00000103966 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:41919376..41919450 32194978 MeRIP-seq:(Medium) rs751987742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27231627 Human_miRNA_ID_2295827 RMVar_hsa_circ_37826,RMVar_hsa_circ_91169,RMVar_hsa_circ_171166,RMVar_hsa_circ_327379 61829 RMVar_ID_61829 Human_SNP_ID_574845338 m1A Human chr15 - 41919427 41919427 41919427 CCAAGTGGACACGCAGCAGCTGATGCGGGTCTACGGGGCCCTCATGTGGTCCCTAGGCAAGGTCA CCAAGTGGACACGCAGCAGCTGATGCGGGTCTCCGGGGCCCTCATGTGGTCCCTAGGCAAGGTCA T G EHD4 Ensembl:ENSG00000103966 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:41919376..41919450 32194978 MeRIP-seq:(Medium) rs751987742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27231627 Human_miRNA_ID_2295827 RMVar_hsa_circ_37826,RMVar_hsa_circ_91169,RMVar_hsa_circ_171166,RMVar_hsa_circ_327379 61830 RMVar_ID_61830 Human_SNP_ID_574858125 m1A Human chr15 - 41972250 41972250 41972250 CACCGGCAAGACCACCTTCATCAGGTACCGTCACCGCCCCTCGCCCGGCTCCCGCCCCGCTCCGC CACCGGCAAGACCACCTTCATCAGGTACCGTCCCCGCCCCTCGCCCGGCTCCCGCCCCGCTCCGC T G EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:41972249..41972540 26863196 MeRIP-seq:(Medium) rs1217526482 Functional Loss SNV dbSNP153 33..33 33 - - - 61831 RMVar_ID_61831 Human_SNP_ID_574858252 m1A Human chr15 - 41972513 41972513 41972513 GGAGAGTCGAACCCGGAGCAGGGTCCCATCCGAGCGTGGACTGGCGGCAGGATGTTCAGCTGGAT GGAGAGTCGAACCCGGAGCAGGGTCCCATCCGTGCGTGGACTGGCGGCAGGATGTTCAGCTGGAT T A EHD4 Ensembl:ENSG00000103966 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:41972276..41972600;chr15:41972301..41972600 26863196 MeRIP-seq:(Medium) rs1345323758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343051,Human_RBP_ID_23127357 61832 RMVar_ID_61832 Human_SNP_ID_574858253 m1A Human chr15 - 41972513 41972513 41972513 GGAGAGTCGAACCCGGAGCAGGGTCCCATCCGAGCGTGGACTGGCGGCAGGATGTTCAGCTGGAT GGAGAGTCGAACCCGGAGCAGGGTCCCATCCGCGCGTGGACTGGCGGCAGGATGTTCAGCTGGAT T G EHD4 Ensembl:ENSG00000103966 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:41972276..41972600;chr15:41972301..41972600 26863196 MeRIP-seq:(Medium) rs1345323758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343051,Human_RBP_ID_23127357 61833 RMVar_ID_61833 Human_SNP_ID_574858256 m1A Human chr15 + 41972517 41972517 41972517 AGCTGAACATCCTGCCGCCAGTCCACGCTCGGATGGGACCCTGCTCCGGGTTCGACTCTCCCCGG AGCTGAACATCCTGCCGCCAGTCCACGCTCGGCTGGGACCCTGCTCCGGGTTCGACTCTCCCCGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:41972319..41972575 26863196 MeRIP-seq:(Medium) rs1279760588 Functional Loss SNV dbSNP153 33..33 33 - - - 61834 RMVar_ID_61834 Human_SNP_ID_574935485 m1A Human chr15 + 42273361 42273361 42273361 GTGGTGACGGGTGAGCTCCCAGAAGCAGAAGAATGACAGGCAACACCTGAAGCCACGCAGCCGCC GTGGTGACGGGTGAGCTCCCAGAAGCAGAAGAGTGACAGGCAACACCTGAAGCCACGCAGCCGCC A G GANC Ensembl:ENSG00000214013 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:42273312..42273402 26863196 MeRIP-seq:(Medium) rs1408670544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1589221 61835 RMVar_ID_61835 Human_SNP_ID_574991956 m1A Human chr15 + 42491028 42491028 42491028 TCTTACTCCATCAGGCCGCCGAGAGCCAGGCGAGGGAGCTCCCTGACGCCTCAGACGCCCCCTTC TCTTACTCCATCAGGCCGCCGAGAGCCAGGCGCGGGAGCTCCCTGACGCCTCAGACGCCCCCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:42490939..42491053;chr15:42490922..42491127;chr15:42490925..42491078 26863196 MeRIP-seq:(Medium) rs1469201735 Functional Loss SNV dbSNP153 33..33 33 - - - 61836 RMVar_ID_61836 Human_SNP_ID_575006170 m1A Human chr15 + 42548732 42548732 42548732 CGCTCAGCTGCCGTAAGGCTCCGCAGGTGAAGACCCAGGACCCGCAGTAGCCGGGATGCGCTCCC CGCTCAGCTGCCGTAAGGCTCCGCAGGTGAAGGCCCAGGACCCGCAGTAGCCGGGATGCGCTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:42548665..42548733 26863196 MeRIP-seq:(Medium) rs1224175294 Functional Loss SNV dbSNP153 33..33 33 - - - 61837 RMVar_ID_61837 Human_SNP_ID_575006614 m1A Human chr15 + 42549832 42549832 42549832 AAAAGATAAGACCTTGGAACGTGAATGGAGGAAGAGATTAATTTTGAGAAGGAGAGAAAAGAGAC AAAAGATAAGACCTTGGAACGTGAATGGAGGACGAGATTAATTTTGAGAAGGAGAGAAAAGAGAC A C HAUS2 Ensembl:ENSG00000137814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:42549795..42550008 26863196 MeRIP-seq:(Medium) rs1183267036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12509183 61838 RMVar_ID_61838 Human_SNP_ID_575013769 m1A Human chr15 - 42575666 42575654 42575667 AGTCCAGCGGGTCAGCTCAGCGGCAGCATCCCAGGCCCCCGCCCTAAGCCCAGACACAGCCCCAA AGTCCAGCGGGTCAGCTCAGCGGCAGCATCC_____________TAAGCCCAGACACAGCCCCAA AGGGCGGGGGCCTG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:42575607..42575803 26863196 MeRIP-seq:(Medium) rs1343897406 Functional Loss DEL dbSNP153 32..44 33 - - - 61839 RMVar_ID_61839 Human_SNP_ID_575026946 m1A Human chr15 - 42626322 42626319 42626323 AGAAGAGGAAGAGGAAGAAGAGGAAGAGGAGGAAGAAGAGGAAGAGGAAGAAGGGGAGGAAGAGG AGAAGAGGAAGAGGAAGAAGAGGAAGAGGAG____AAGAGGAAGAGGAAGAAGGGGAGGAAGAGG TCTTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:42626292..42626407 26863196 MeRIP-seq:(Medium) rs1398098158 Functional Loss DEL dbSNP153 32..35 33 - - - 61840 RMVar_ID_61840 Human_SNP_ID_575027034 m1A Human chr15 - 42626405 42626390 42626405 GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAAGAGGA GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGA_______________GGAAGAGGAGGAAGAGGA CTCTTCCTCCTCCTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42626341..42626434 26863196 MeRIP-seq:(Medium) rs1180107107 Functional Loss DEL dbSNP153 33..47 33 - - - 61841 RMVar_ID_61841 Human_SNP_ID_575027049 m1A Human chr15 - 42626405 42626402 42626405 GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAAGAGGA GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGA___GGAGGAGGAAGAGGAAGAGGAGGAAGAGGA CTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42626341..42626434 26863196 MeRIP-seq:(Medium) rs1277986506 Functional Loss DEL dbSNP153 33..35 33 - - - 61842 RMVar_ID_61842 Human_SNP_ID_575027053 m1A Human chr15 - 42626405 42626405 42626405 GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAAGAGGA GAAGAAGAAGAAGAGGAGGAGGAGGAGGAAGAGGAGGAGGAGGAAGAGGAAGAGGAGGAAGAGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42626341..42626434 26863196 MeRIP-seq:(Medium) rs904630493 Functional Loss SNV dbSNP153 33..33 33 - - - 61843 RMVar_ID_61843 Human_SNP_ID_575038702 m1A Human chr15 + 42671642 42671628 42671643 AATAAGGAAAGGAATGTGAGCTGGTACTGATAACGCTGGTACTGTGGCATGTCTGGGCATGTAAT AATAAGGAAAGGAATGTGA_______________GCTGGTACTGTGGCATGTCTGGGCATGTAAT AGCTGGTACTGATAAC A STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42671605..42671785 26863196 MeRIP-seq:(Medium) rs1477809965 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_12509708 RMVar_hsa_circ_97055,RMVar_hsa_circ_67386,RMVar_hsa_circ_264954,RMVar_hsa_circ_106436,RMVar_hsa_circ_97565,RMVar_hsa_circ_171243,RMVar_hsa_circ_171244,RMVar_hsa_circ_171242,RMVar_hsa_circ_362722,RMVar_hsa_circ_21999,RMVar_hsa_circ_77169,RMVar_hsa_circ_35838,RMVar_hsa_circ_94192,RMVar_hsa_circ_171249,RMVar_hsa_circ_171248,RMVar_hsa_circ_171251,RMVar_hsa_circ_95074,RMVar_hsa_circ_266167,RMVar_hsa_circ_106823,RMVar_hsa_circ_126355,RMVar_hsa_circ_171253,RMVar_hsa_circ_121702,RMVar_hsa_circ_171255,RMVar_hsa_circ_292269,RMVar_hsa_circ_171256 61844 RMVar_ID_61844 Human_SNP_ID_575059359 m1A Human chr15 - 42737071 42737071 42737071 GATGGCGGCCGTTTTGGAGTCGCTGCTGCGAGAAGAGGTGTCGGTCGCAGCCGTCGTGCGGTGGA GATGGCGGCCGTTTTGGAGTCGCTGCTGCGAGGAGAGGTGTCGGTCGCAGCCGTCGTGCGGTGGA T C CDAN1 Ensembl:ENSG00000140326 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:42736602..42737102 26863196 MeRIP-seq:(Medium) rs1214359424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342614 Human_Splice_Rec_1591245,Human_Splice_Rec_1591327,Human_Splice_Rec_1591377 61845 RMVar_ID_61845 Human_SNP_ID_575059365 m1A Human chr15 + 42737077 42737077 42737077 GCACGACGGCTGCGACCGACACCTCTTCTCGCAGCAGCGACTCCAAAACGGCCGCCATCCCGGTC GCACGACGGCTGCGACCGACACCTCTTCTCGCGGCAGCGACTCCAAAACGGCCGCCATCCCGGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42736963..42737086 26863196 MeRIP-seq:(Medium) rs1441801566 Functional Loss SNV dbSNP153 33..33 33 - - - 61846 RMVar_ID_61846 Human_SNP_ID_575059366 m1A Human chr15 + 42737077 42737077 42737077 GCACGACGGCTGCGACCGACACCTCTTCTCGCAGCAGCGACTCCAAAACGGCCGCCATCCCGGTC GCACGACGGCTGCGACCGACACCTCTTCTCGCTGCAGCGACTCCAAAACGGCCGCCATCCCGGTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42736963..42737086 26863196 MeRIP-seq:(Medium) rs1441801566 Functional Loss SNV dbSNP153 33..33 33 - - - 61847 RMVar_ID_61847 Human_SNP_ID_575092007 m1A Human chr15 + 42872741 42872741 42872741 TCCAAGGCATCGTAAATTTCTCCAAAGCCCCCACCCCCAATCTTTCTCAACTGCACAGAAAATAA TCCAAGGCATCGTAAATTTCTCCAAAGCCCCCTCCCCCAATCTTTCTCAACTGCACAGAAAATAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:42872691..42878651 26863196 MeRIP-seq:(Medium) rs1375359928 Functional Loss SNV dbSNP153 33..33 33 - - - 61848 RMVar_ID_61848 Human_SNP_ID_575103536 m1A Human chr15 + 42920779 42920778 42920779 ACCGCTCCCATCGCCGCTGCGGCGACTACTGCAGAGCCCGCTGACCCGACCCGACGTTATTCTCC ACCGCTCCCATCGCCGCTGCGGCGACTACTGC_GAGCCCGCTGACCCGACCCGACGTTATTCTCC CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr15:42920462..42920819;chr15:42920676..42920813 26863196 MeRIP-seq:(Medium) rs1179871002 Functional Loss DEL dbSNP153 33..33 33 - - - 61849 RMVar_ID_61849 Human_SNP_ID_575117594 m1A Human chr15 + 42981374 42981374 42981374 TGTTCAAATGTGCCCTGTGTCTTTTGGAATGCAGCTTCTGTTCCTCTCAATTTATCTATTATGTG TGTTCAAATGTGCCCTGTGTCTTTTGGAATGCGGCTTCTGTTCCTCTCAATTTATCTATTATGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:42981329..42981412 26863196 MeRIP-seq:(Medium) rs931563004 Functional Loss SNV dbSNP153 33..33 33 - - - 61850 RMVar_ID_61850 Human_SNP_ID_575151484 m1A Human chr15 - 43115654 43115654 43115654 AAATAGTGGCAAATAAAAAGTGCTATTTGTGAAAAAAAAAAAAAAAAAAAAAAAAAGACAAAAAC AAATAGTGGCAAATAAAAAGTGCTATTTGTGAGAAAAAAAAAAAAAAAAAAAAAAAGACAAAAAC T C AC068724.4 Ensembl:ENSG00000285080 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1382379527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457536,Human_RBP_ID_9052278,Human_RBP_ID_23652004,Human_RBP_ID_26433959,Human_RBP_ID_26931461 61851 RMVar_ID_61851 Human_SNP_ID_575155683 m1A Human chr15 - 43133655 43133655 43133655 GCGGGGCCGGCGCCGGATGCGGGGCTGGAGCCAGACACTGGGCCTAGGGTGCTGCGCCCGTCAGC GCGGGGCCGGCGCCGGATGCGGGGCTGGAGCCGGACACTGGGCCTAGGGTGCTGCGCCCGTCAGC T C AC068724.4 Ensembl:ENSG00000285080 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43133606..43133768 26863196 MeRIP-seq:(Medium) rs1353826577 Functional Loss SNV dbSNP153 33..33 33 - - - 61852 RMVar_ID_61852 Human_SNP_ID_575167517 m1A Human chr15 + 43185875 43185875 43185875 GAGGAGTTTAATCGAGAGATGTTCTGGAGAAGACTCAGTGAGTGCGCCTCCTTCCGGGCTCCCCT GAGGAGTTTAATCGAGAGATGTTCTGGAGAAGGCTCAGTGAGTGCGCCTCCTTCCGGGCTCCCCT A G CCNDBP1 Ensembl:ENSG00000166946 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43185825..43185926 32194978 MeRIP-seq:(Medium) rs1286919173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1591884,Human_Splice_Rec_1591898,Human_Splice_Rec_1591899,Human_Splice_Rec_1591920,Human_Splice_Rec_1591921,Human_Splice_Rec_1591956,Human_Splice_Rec_1591957,Human_Splice_Rec_1591982,Human_Splice_Rec_1591983,Human_Splice_Rec_1591988,Human_Splice_Rec_1591989,Human_Splice_Rec_1592006,Human_Splice_Rec_1592007,Human_Splice_Rec_1592026,Human_Splice_Rec_1592027 RMVar_hsa_circ_90732,RMVar_hsa_circ_171423 61853 RMVar_ID_61853 Human_SNP_ID_575203148 m1A Human chr15 - 43330071 43330071 43330071 GCCAGAGCTGTGCGCGTTAACCGGGCCTTTCGAGAGGGGGGAGCCCGCGTCCGCGCTGTGCTTTG GCCAGAGCTGTGCGCGTTAACCGGGCCTTTCGCGAGGGGGGAGCCCGCGTCCGCGCTGTGCTTTG T G LCMT2 Ensembl:ENSG00000168806 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43330021..43330097 26863196 MeRIP-seq:(Medium) rs754423088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22048197 61854 RMVar_ID_61854 Human_SNP_ID_575213241 m1A Human chr15 - 43369002 43369002 43369002 GTGGAACCCCAGCCCAGGGGTGTACCCAAGAAAGAGAGGGCAAGAAGCCCAGACCTGGGACCACA GTGGAACCCCAGCCCAGGGGTGTACCCAAGAAGGAGAGGGCAAGAAGCCCAGACCTGGGACCACA T C ZSCAN29 Ensembl:ENSG00000140265 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:43368951..43369051 32194978 MeRIP-seq:(Medium) rs751145031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5523299,Human_RBP_ID_9283998 Human_Splice_Rec_1592463,Human_Splice_Rec_1592471,Human_Splice_Rec_1592479,Human_Splice_Rec_1592487,Human_Splice_Rec_1592495,Human_Splice_Rec_1592499 RMVar_hsa_circ_66243 61855 RMVar_ID_61855 Human_SNP_ID_575213829 m1A Human chr15 + 43370975 43370975 43370975 GGCCAGCCTCACCCACTCGGGGTCCGACCCTGACCCCGGCCCCGGCCCCGGCCCCGGCCCCGGCT GGCCAGCCTCACCCACTCGGGGTCCGACCCTGGCCCCGGCCCCGGCCCCGGCCCCGGCCCCGGCT A G TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:43370857..43371027 26863196 MeRIP-seq:(Medium) rs3840834 Functional Loss SNV dbSNP153 33..33 33 - - - 61856 RMVar_ID_61856 Human_SNP_ID_575213869 m1A Human chr15 - 43371007 43371001 43371007 CCGGTTTGGGAGCTGTACTTGGGAGGCTGGAGAGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGT CCGGTTTGGGAGCTGTACTTGGGAGGCTGGAG______GGCCGGGGCCGGGGCCGGGGCCGGGGT CCCGGCT C ZSCAN29 Ensembl:ENSG00000140265 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43370650..43371019 26863196 MeRIP-seq:(Medium) rs935241174 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4342260,Human_RBP_ID_9353033,Human_RBP_ID_18418348 61857 RMVar_ID_61857 Human_SNP_ID_575213878 m1A Human chr15 - 43371007 43371007 43371007 CCGGTTTGGGAGCTGTACTTGGGAGGCTGGAGAGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGT CCGGTTTGGGAGCTGTACTTGGGAGGCTGGAGCGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGT T G ZSCAN29 Ensembl:ENSG00000140265 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43370650..43371019 26863196 MeRIP-seq:(Medium) rs1372175731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342260,Human_RBP_ID_9353033,Human_RBP_ID_18418348 61858 RMVar_ID_61858 Human_SNP_ID_575217258 m1A Human chr15 + 43384973 43384973 43384973 AGAGATGTTTAGAGGGTGGAATCAGTAGGCTTAGTGAGTGCTTGGAAATGAGTCAAGAGGGAAGA AGAGATGTTTAGAGGGTGGAATCAGTAGGCTTCGTGAGTGCTTGGAAATGAGTCAAGAGGGAAGA A C TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43384970..43385128 26863196 MeRIP-seq:(Medium) rs542188416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2440913 RMVar_hsa_circ_88554,RMVar_hsa_circ_339561,RMVar_hsa_circ_110580,RMVar_hsa_circ_171444,RMVar_hsa_circ_171445,RMVar_hsa_circ_12149,RMVar_hsa_circ_171450,RMVar_hsa_circ_333823,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_308480 61859 RMVar_ID_61859 Human_SNP_ID_575217259 m1A Human chr15 + 43384973 43384973 43384973 AGAGATGTTTAGAGGGTGGAATCAGTAGGCTTAGTGAGTGCTTGGAAATGAGTCAAGAGGGAAGA AGAGATGTTTAGAGGGTGGAATCAGTAGGCTTGGTGAGTGCTTGGAAATGAGTCAAGAGGGAAGA A G TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43384970..43385128 26863196 MeRIP-seq:(Medium) rs542188416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2440913 RMVar_hsa_circ_88554,RMVar_hsa_circ_339561,RMVar_hsa_circ_110580,RMVar_hsa_circ_171444,RMVar_hsa_circ_171445,RMVar_hsa_circ_12149,RMVar_hsa_circ_171450,RMVar_hsa_circ_333823,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_308480 61860 RMVar_ID_61860 Human_SNP_ID_575222113 m1A Human chr15 + 43403463 43403455 43403464 TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTAAGAGAGTAATACTCGCTTAGCCAGGAAAGGATG TGTGGCTAGATTGGAGGTTTGGTGC_________AGAGTAATACTCGCTTAGCCAGGAAAGGATG CAGGGCTAAG C TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43403460..43403611 32194978 MeRIP-seq:(Medium) rs1248619288 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_22496266 RMVar_hsa_circ_110580,RMVar_hsa_circ_171445,RMVar_hsa_circ_8267,RMVar_hsa_circ_22718,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_62632,RMVar_hsa_circ_373827,RMVar_hsa_circ_171457,RMVar_hsa_circ_291432,RMVar_hsa_circ_374302,RMVar_hsa_circ_171462,RMVar_hsa_circ_171464 61861 RMVar_ID_61861 Human_SNP_ID_575222115 m1A Human chr15 + 43403463 43403461 43403463 TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTAAGAGAGTAATACTCGCTTAGCCAGGAAAGGATG TGTGGCTAGATTGGAGGTTTGGTGCAGGGCT__GAGAGTAATACTCGCTTAGCCAGGAAAGGATG TAA T TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43403460..43403611 32194978 MeRIP-seq:(Medium) rs1451064025 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22496266 RMVar_hsa_circ_110580,RMVar_hsa_circ_171445,RMVar_hsa_circ_8267,RMVar_hsa_circ_22718,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_62632,RMVar_hsa_circ_373827,RMVar_hsa_circ_171457,RMVar_hsa_circ_291432,RMVar_hsa_circ_374302,RMVar_hsa_circ_171462,RMVar_hsa_circ_171464 61862 RMVar_ID_61862 Human_SNP_ID_575222117 m1A Human chr15 + 43403463 43403462 43403464 TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTAAGAGAGTAATACTCGCTTAGCCAGGAAAGGATG TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTA__AGAGTAATACTCGCTTAGCCAGGAAAGGATG AAG A TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43403460..43403611 32194978 MeRIP-seq:(Medium) rs1251436574 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22496266 RMVar_hsa_circ_110580,RMVar_hsa_circ_171445,RMVar_hsa_circ_8267,RMVar_hsa_circ_22718,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_62632,RMVar_hsa_circ_373827,RMVar_hsa_circ_171457,RMVar_hsa_circ_291432,RMVar_hsa_circ_374302,RMVar_hsa_circ_171462,RMVar_hsa_circ_171464 61863 RMVar_ID_61863 Human_SNP_ID_575222118 m1A Human chr15 + 43403463 43403463 43403463 TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTAAGAGAGTAATACTCGCTTAGCCAGGAAAGGATG TGTGGCTAGATTGGAGGTTTGGTGCAGGGCTAGGAGAGTAATACTCGCTTAGCCAGGAAAGGATG A G TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43403460..43403611 32194978 MeRIP-seq:(Medium) rs970883876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22496266 RMVar_hsa_circ_110580,RMVar_hsa_circ_171445,RMVar_hsa_circ_8267,RMVar_hsa_circ_22718,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_62632,RMVar_hsa_circ_373827,RMVar_hsa_circ_171457,RMVar_hsa_circ_291432,RMVar_hsa_circ_374302,RMVar_hsa_circ_171462,RMVar_hsa_circ_171464 61864 RMVar_ID_61864 Human_SNP_ID_575236312 m1A Human chr15 - 43456988 43456988 43456988 TCCCCAAAGATGGAGAGCTTGAGTTCTCACAGAATTGATGAAGATGGAGAAAACACACAGATTGA TCCCCAAAGATGGAGAGCTTGAGTTCTCACAGGATTGATGAAGATGGAGAAAACACACAGATTGA T C TP53BP1 Ensembl:ENSG00000067369 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43456946..43457047 32194978 MeRIP-seq:(Medium) rs774356134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1829535,Human_RBP_ID_18662918 RMVar_hsa_circ_107044,RMVar_hsa_circ_171466,RMVar_hsa_circ_104974,RMVar_hsa_circ_889,RMVar_hsa_circ_171468,RMVar_hsa_circ_53912,RMVar_hsa_circ_126188,RMVar_hsa_circ_171472,RMVar_hsa_circ_171473,RMVar_hsa_circ_34296,RMVar_hsa_circ_93271,RMVar_hsa_circ_171477,RMVar_hsa_circ_266969,RMVar_hsa_circ_310538,RMVar_hsa_circ_319384,RMVar_hsa_circ_171481,RMVar_hsa_circ_372782,RMVar_hsa_circ_171484,RMVar_hsa_circ_374300,RMVar_hsa_circ_110231,RMVar_hsa_circ_171488,RMVar_hsa_circ_171486,RMVar_hsa_circ_294938,RMVar_hsa_circ_300810,RMVar_hsa_circ_171491,RMVar_hsa_circ_348781,RMVar_hsa_circ_370637,RMVar_hsa_circ_328789,RMVar_hsa_circ_61746,RMVar_hsa_circ_171494,RMVar_hsa_circ_292949,RMVar_hsa_circ_171492,RMVar_hsa_circ_322021,RMVar_hsa_circ_280711,RMVar_hsa_circ_171493 61865 RMVar_ID_61865 Human_SNP_ID_575242259 m1A Human chr15 - 43479503 43479503 43479503 AACTCTCAGCAATTAAGCATGAAGAACAGTCCAACGAAGATATCCCCATAGCAGAACAGTCCAGC AACTCTCAGCAATTAAGCATGAAGAACAGTCCGACGAAGATATCCCCATAGCAGAACAGTCCAGC T C TP53BP1 Ensembl:ENSG00000067369 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43477635..43479905 32194978 MeRIP-seq:(Medium) rs1407777406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885008,Human_RBP_ID_1829549,Human_RBP_ID_3945458,Human_RBP_ID_5523306,Human_RBP_ID_9371516,Human_RBP_ID_12654428,Human_RBP_ID_17860597,Human_RBP_ID_27435272 Human_Splice_Rec_1592678,Human_Splice_Rec_1592732,Human_Splice_Rec_1592832,Human_Splice_Rec_1592884,Human_Splice_Rec_1592952,Human_Splice_Rec_1593010 Human_miRNA_ID_1981012,Human_miRNA_ID_1982736 RMVar_hsa_circ_789,RMVar_hsa_circ_171466,RMVar_hsa_circ_104974,RMVar_hsa_circ_889,RMVar_hsa_circ_171468,RMVar_hsa_circ_310538,RMVar_hsa_circ_171481,RMVar_hsa_circ_171488,RMVar_hsa_circ_294938,RMVar_hsa_circ_171491,RMVar_hsa_circ_370637,RMVar_hsa_circ_322021,RMVar_hsa_circ_171496,RMVar_hsa_circ_323204,RMVar_hsa_circ_52051,RMVar_hsa_circ_279824,RMVar_hsa_circ_171500,RMVar_hsa_circ_295953,RMVar_hsa_circ_171498,RMVar_hsa_circ_275021,RMVar_hsa_circ_171499 61866 RMVar_ID_61866 Human_SNP_ID_575246047 m1A Human chr15 - 43493111 43493111 43493111 GTGGCGGCGGTGGCGACAGCGGCGACCTAGGGATCGATCTGGAGGGACTTGGGGAGCGTGCAGAG GTGGCGGCGGTGGCGACAGCGGCGACCTAGGGGTCGATCTGGAGGGACTTGGGGAGCGTGCAGAG T C TP53BP1 Ensembl:ENSG00000067369 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:43493042..43493147;chr15:43493016..43493133;chr15:43493008..43493127 26863196 MeRIP-seq:(Medium) rs1423718767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814553,Human_RBP_ID_4342625,Human_RBP_ID_5418568,Human_RBP_ID_8803823,Human_RBP_ID_9283629,Human_RBP_ID_18418349 Human_Splice_Rec_1592667,Human_Splice_Rec_1592821,Human_Splice_Rec_1592873,Human_Splice_Rec_1592941,Human_Splice_Rec_1592999 61867 RMVar_ID_61867 Human_SNP_ID_575246048 m1A Human chr15 - 43493111 43493111 43493111 GTGGCGGCGGTGGCGACAGCGGCGACCTAGGGATCGATCTGGAGGGACTTGGGGAGCGTGCAGAG GTGGCGGCGGTGGCGACAGCGGCGACCTAGGGCTCGATCTGGAGGGACTTGGGGAGCGTGCAGAG T G TP53BP1 Ensembl:ENSG00000067369 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:43493042..43493147;chr15:43493016..43493133;chr15:43493008..43493127 26863196 MeRIP-seq:(Medium) rs1423718767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814553,Human_RBP_ID_4342625,Human_RBP_ID_5418568,Human_RBP_ID_8803823,Human_RBP_ID_9283629,Human_RBP_ID_18418349 Human_Splice_Rec_1592667,Human_Splice_Rec_1592821,Human_Splice_Rec_1592873,Human_Splice_Rec_1592941,Human_Splice_Rec_1592999 61868 RMVar_ID_61868 Human_SNP_ID_575253537 m1A Human chr15 + 43523390 43523390 43523390 AGGGAAGCAGAGAGGCTCCCAGACAGAACAGAAGCCAGAGAGGAAAGTGAACCTGAAGTAAAGGA AGGGAAGCAGAGAGGCTCCCAGACAGAACAGACGCCAGAGAGGAAAGTGAACCTGAAGTAAAGGA A C MAP1A Ensembl:ENSG00000166963 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:43523354..43523438 26863196 MeRIP-seq:(Medium) rs768447122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110155,RMVar_hsa_circ_112964,RMVar_hsa_circ_96924,RMVar_hsa_circ_171501,RMVar_hsa_circ_171502,RMVar_hsa_circ_171503 61869 RMVar_ID_61869 Human_SNP_ID_575278900 m1A Human chr15 - 43648654 43648654 43648654 GAGCTGGAGGCGGAAGCGTGAAATAAGGACTGAGTGGGCAAAGAGAACCTGGGCTGAGGTGAGGC GAGCTGGAGGCGGAAGCGTGAAATAAGGACTGCGTGGGCAAAGAGAACCTGGGCTGAGGTGAGGC T G CATSPER2 Ensembl:ENSG00000166762 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43648639..43648788 26863196 MeRIP-seq:(Medium) rs1028151183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12513162,Human_RBP_ID_23652350 Human_Splice_Rec_1594181,Human_Splice_Rec_1594236,Human_Splice_Rec_1594237,Human_Splice_Rec_1594261,Human_Splice_Rec_1594307 RMVar_hsa_circ_171526,RMVar_hsa_circ_97014 61870 RMVar_ID_61870 Human_SNP_ID_575296095 m1A Human chr15 + 43746082 43746082 43746082 CAGCCCAGGTTCTCTTCGCCCACTCAGTCCTGACTTCACGCTTCCACCTCCAGCTCAGGCGCCCC CAGCCCAGGTTCTCTTCGCCCACTCAGTCCTGCCTTCACGCTTCCACCTCCAGCTCAGGCGCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43746056..43746249 26863196 MeRIP-seq:(Medium) rs1034107462 Functional Loss SNV dbSNP153 33..33 33 - - - 61871 RMVar_ID_61871 Human_SNP_ID_575296275 m1A Human chr15 + 43746464 43746464 43746464 TGGGCCAGACGCGCGAGCGCAAGCAGCGGGTTAGTGGTCGCGCGCCCGACCTCCGCAGTCCCAGC TGGGCCAGACGCGCGAGCGCAAGCAGCGGGTTTGTGGTCGCGCGCCCGACCTCCGCAGTCCCAGC A T PDIA3 Ensembl:ENSG00000167004 Protein coding exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:43746426..43746500;chr15:43746426..43746525;chr15:43746401..43746525;chr15:43746401..43746650;chr15:43746401..43746536 26863196 MeRIP-seq:(Medium) rs4080718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42519,Human_RBP_ID_123393,Human_RBP_ID_232292,Human_RBP_ID_457662,Human_RBP_ID_759173,Human_RBP_ID_815239,Human_RBP_ID_1000690,Human_RBP_ID_4342262,Human_RBP_ID_8804069,Human_RBP_ID_9283633,Human_RBP_ID_22532615,Human_RBP_ID_23652360 RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 61872 RMVar_ID_61872 Human_SNP_ID_575299123 m1A Human chr15 + 43756725 43756725 43756725 CAGTGGATATCCAACCCTGAAGATATTTAGAGATGGTGAAGAAGCAGGTGCTTATGATGGACCTA CAGTGGATATCCAACCCTGAAGATATTTAGAGCTGGTGAAGAAGCAGGTGCTTATGATGGACCTA A C PDIA3 Ensembl:ENSG00000167004 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43756676..43756817 26863196 MeRIP-seq:(Medium) rs746916199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457663,Human_RBP_ID_1504686,Human_RBP_ID_1829561,Human_RBP_ID_3474609,Human_RBP_ID_17870101,Human_RBP_ID_22440282,Human_RBP_ID_22758781,Human_RBP_ID_22934562,Human_RBP_ID_27650938 Human_Splice_Rec_1594546,Human_Splice_Rec_1594550,Human_Splice_Rec_1594551,Human_Splice_Rec_1594576,Human_Splice_Rec_1594582,Human_Splice_Rec_1594583,Human_Splice_Rec_1594606,Human_Splice_Rec_1594607 RMVar_hsa_circ_93618,RMVar_hsa_circ_12384,RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532,RMVar_hsa_circ_285234,RMVar_hsa_circ_334385,RMVar_hsa_circ_342005,RMVar_hsa_circ_285307,RMVar_hsa_circ_122670,RMVar_hsa_circ_171533,RMVar_hsa_circ_171534,RMVar_hsa_circ_171535,RMVar_hsa_circ_288441,RMVar_hsa_circ_355242,RMVar_hsa_circ_119058,RMVar_hsa_circ_171536,RMVar_hsa_circ_171537,RMVar_hsa_circ_171538 61873 RMVar_ID_61873 Human_SNP_ID_575299124 m1A Human chr15 + 43756725 43756725 43756725 CAGTGGATATCCAACCCTGAAGATATTTAGAGATGGTGAAGAAGCAGGTGCTTATGATGGACCTA CAGTGGATATCCAACCCTGAAGATATTTAGAGGTGGTGAAGAAGCAGGTGCTTATGATGGACCTA A G PDIA3 Ensembl:ENSG00000167004 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43756676..43756817 26863196 MeRIP-seq:(Medium) rs746916199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457663,Human_RBP_ID_1504686,Human_RBP_ID_1829561,Human_RBP_ID_3474609,Human_RBP_ID_17870101,Human_RBP_ID_22440282,Human_RBP_ID_22758781,Human_RBP_ID_22934562,Human_RBP_ID_27650938 Human_Splice_Rec_1594546,Human_Splice_Rec_1594550,Human_Splice_Rec_1594551,Human_Splice_Rec_1594576,Human_Splice_Rec_1594582,Human_Splice_Rec_1594583,Human_Splice_Rec_1594606,Human_Splice_Rec_1594607 RMVar_hsa_circ_93618,RMVar_hsa_circ_12384,RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532,RMVar_hsa_circ_285234,RMVar_hsa_circ_334385,RMVar_hsa_circ_342005,RMVar_hsa_circ_285307,RMVar_hsa_circ_122670,RMVar_hsa_circ_171533,RMVar_hsa_circ_171534,RMVar_hsa_circ_171535,RMVar_hsa_circ_288441,RMVar_hsa_circ_355242,RMVar_hsa_circ_119058,RMVar_hsa_circ_171536,RMVar_hsa_circ_171537,RMVar_hsa_circ_171538 61874 RMVar_ID_61874 Human_SNP_ID_575300937 m1A Human chr15 + 43763101 43763101 43763101 CTGTATAGGTTTTTTCGATGATTCATTCAGTGAGGCTCACTCCGAGTTCCTAAAAGCAGCCAGCA CTGTATAGGTTTTTTCGATGATTCATTCAGTGGGGCTCACTCCGAGTTCCTAAAAGCAGCCAGCA A G PDIA3 Ensembl:ENSG00000167004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43763063..43763142 26863196 MeRIP-seq:(Medium) rs1444662774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232295,Human_RBP_ID_759181,Human_RBP_ID_2441071,Human_RBP_ID_17366886,Human_RBP_ID_17688478,Human_RBP_ID_22387929,Human_RBP_ID_22758786,Human_RBP_ID_22928760,Human_RBP_ID_24412306,Human_RBP_ID_25140195,Human_RBP_ID_26931617 Human_Splice_Rec_1594554,Human_Splice_Rec_1594586 Human_miRNA_ID_2209195,Human_miRNA_ID_3033800 RMVar_hsa_circ_93618,RMVar_hsa_circ_12384,RMVar_hsa_circ_114800,RMVar_hsa_circ_171532,RMVar_hsa_circ_334385,RMVar_hsa_circ_342005,RMVar_hsa_circ_122670,RMVar_hsa_circ_171534,RMVar_hsa_circ_171535,RMVar_hsa_circ_288441,RMVar_hsa_circ_355242,RMVar_hsa_circ_119058,RMVar_hsa_circ_42561,RMVar_hsa_circ_46622,RMVar_hsa_circ_171536,RMVar_hsa_circ_171537,RMVar_hsa_circ_171538,RMVar_hsa_circ_331945,RMVar_hsa_circ_352735,RMVar_hsa_circ_270253,RMVar_hsa_circ_319879,RMVar_hsa_circ_370205,RMVar_hsa_circ_171539,RMVar_hsa_circ_372953,RMVar_hsa_circ_330285,RMVar_hsa_circ_299251,RMVar_hsa_circ_171541,RMVar_hsa_circ_171542,RMVar_hsa_circ_171540 61875 RMVar_ID_61875 Human_SNP_ID_575309029 m1A Human chr15 + 43792069 43792069 43792069 CGAGCCCGCGGGAGCGCCACATCGCCAGCCGCACCCCTCCACCCCCAACCTGCCCACGTGACCCG CGAGCCCGCGGGAGCGCCACATCGCCAGCCGCCCCCCTCCACCCCCAACCTGCCCACGTGACCCG A C SERF2 Ensembl:ENSG00000140264 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:43792018..43792118 32194978 MeRIP-seq:(Medium) rs1310022216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1594736 RMVar_hsa_circ_91551,RMVar_hsa_circ_171547 61876 RMVar_ID_61876 Human_SNP_ID_575309076 m1A Human chr15 + 43792184 43792184 43792184 CACGCTGAGCGCTCCGCCTGCGACCCTCCGCCACTTACCCACCCCGGCTCAAGCACGACCCGTGG CACGCTGAGCGCTCCGCCTGCGACCCTCCGCCGCTTACCCACCCCGGCTCAAGCACGACCCGTGG A G SERF2 Ensembl:ENSG00000140264 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43792117..43792218 26863196 MeRIP-seq:(Medium) rs1461265922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91551,RMVar_hsa_circ_171547 61877 RMVar_ID_61877 Human_SNP_ID_575309176 m1A Human chr15 + 43792377 43792377 43792377 AACGGAGGCAGGTTGGAGCCGCTGCCGTCGCCATGACCCGTGAGCACCGAGCCCCCTTCTCCTTG AACGGAGGCAGGTTGGAGCCGCTGCCGTCGCCCTGACCCGTGAGCACCGAGCCCCCTTCTCCTTG A C SERF2 Ensembl:ENSG00000140264 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:43792326..43792400 26863196 MeRIP-seq:(Medium) rs111392388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232139,Human_RBP_ID_457710,Human_RBP_ID_758957,Human_RBP_ID_815089,Human_RBP_ID_4342634,Human_RBP_ID_5112856,Human_RBP_ID_5316069,Human_RBP_ID_9324247,Human_RBP_ID_17652112,Human_RBP_ID_22440559,Human_RBP_ID_23652393,Human_RBP_ID_24544295,Human_RBP_ID_25140254,Human_RBP_ID_26326325 Human_Splice_Rec_1594737,Human_Splice_Rec_1594741,Human_Splice_Rec_1594745,Human_Splice_Rec_1594749,Human_Splice_Rec_1594753,Human_Splice_Rec_1594755,Human_Splice_Rec_1594759,Human_Splice_Rec_1594765,Human_Splice_Rec_1594771,Human_Splice_Rec_1594775,Human_Splice_Rec_1594779,Human_Splice_Rec_1594791 RMVar_hsa_circ_91551,RMVar_hsa_circ_171547 61878 RMVar_ID_61878 Human_SNP_ID_575309177 m1A Human chr15 + 43792377 43792377 43792377 AACGGAGGCAGGTTGGAGCCGCTGCCGTCGCCATGACCCGTGAGCACCGAGCCCCCTTCTCCTTG AACGGAGGCAGGTTGGAGCCGCTGCCGTCGCCTTGACCCGTGAGCACCGAGCCCCCTTCTCCTTG A T SERF2 Ensembl:ENSG00000140264 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:43792326..43792400 26863196 MeRIP-seq:(Medium) rs111392388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232139,Human_RBP_ID_457710,Human_RBP_ID_758957,Human_RBP_ID_815089,Human_RBP_ID_4342634,Human_RBP_ID_5112856,Human_RBP_ID_5316069,Human_RBP_ID_9324247,Human_RBP_ID_17652112,Human_RBP_ID_22440559,Human_RBP_ID_23652393,Human_RBP_ID_24544295,Human_RBP_ID_25140254,Human_RBP_ID_26326325 Human_Splice_Rec_1594737,Human_Splice_Rec_1594741,Human_Splice_Rec_1594745,Human_Splice_Rec_1594749,Human_Splice_Rec_1594753,Human_Splice_Rec_1594755,Human_Splice_Rec_1594759,Human_Splice_Rec_1594765,Human_Splice_Rec_1594771,Human_Splice_Rec_1594775,Human_Splice_Rec_1594779,Human_Splice_Rec_1594791 RMVar_hsa_circ_91551,RMVar_hsa_circ_171547 61879 RMVar_ID_61879 Human_SNP_ID_575309180 m1A Human chr15 - 43792385 43792385 43792385 GAAAAGGGCAAGGAGAAGGGGGCTCGGTGCTCACGGGTCATGGCGACGGCAGCGGCTCCAACCTG GAAAAGGGCAAGGAGAAGGGGGCTCGGTGCTCTCGGGTCATGGCGACGGCAGCGGCTCCAACCTG T A AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr15:43792276..43792568;chr15:43792326..43792449;chr15:43792326..43792447;chr15:43792180..43792518;chr15:43792217..43792518;chr15:43792367..43792468 26863196,26863410,26863410,26863196,26863196,32194978 MeRIP-seq:(Medium) rs112021926 Functional Loss SNV dbSNP153 33..33 33 - - - 61880 RMVar_ID_61880 Human_SNP_ID_575309181 m1A Human chr15 - 43792385 43792385 43792385 GAAAAGGGCAAGGAGAAGGGGGCTCGGTGCTCACGGGTCATGGCGACGGCAGCGGCTCCAACCTG GAAAAGGGCAAGGAGAAGGGGGCTCGGTGCTCGCGGGTCATGGCGACGGCAGCGGCTCCAACCTG T C AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr15:43792276..43792568;chr15:43792326..43792449;chr15:43792326..43792447;chr15:43792180..43792518;chr15:43792217..43792518;chr15:43792367..43792468 26863196,26863410,26863410,26863196,26863196,32194978 MeRIP-seq:(Medium) rs112021926 Functional Loss SNV dbSNP153 33..33 33 - - - 61881 RMVar_ID_61881 Human_SNP_ID_575309393 m1A Human chr15 - 43792927 43792927 43792927 TAAAGGTGAGACGCGGGGGCCGCTCTGCCCACACACCGGCGACCCTTCTACCCCAGCGCGGCCAG TAAAGGTGAGACGCGGGGGCCGCTCTGCCCACCCACCGGCGACCCTTCTACCCCAGCGCGGCCAG T G AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:43792925..43793129 26863196 MeRIP-seq:(Medium) rs1339583538 Functional Loss SNV dbSNP153 33..33 33 - - - 61882 RMVar_ID_61882 Human_SNP_ID_575309456 m1A Human chr15 + 43793080 43793080 43793080 AGATGACGGGCTTTCTGCTGCCGCCCGCAAGCAGAGGTAGCCCCAGGGAGGGGAGGGAAAGGGAC AGATGACGGGCTTTCTGCTGCCGCCCGCAAGCGGAGGTAGCCCCAGGGAGGGGAGGGAAAGGGAC A G SERF2 Ensembl:ENSG00000140264 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:43792930..43793135 26863196 MeRIP-seq:(Medium) rs1222320937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758959,Human_RBP_ID_815091,Human_RBP_ID_2441109,Human_RBP_ID_4343074,Human_RBP_ID_5112858,Human_RBP_ID_5141379,Human_RBP_ID_9370821,Human_RBP_ID_17652120,Human_RBP_ID_19067199,Human_RBP_ID_22439771,Human_RBP_ID_26326328,Human_RBP_ID_27809437 Human_Splice_Rec_1594739,Human_Splice_Rec_1594743,Human_Splice_Rec_1594747,Human_Splice_Rec_1594751,Human_Splice_Rec_1594757,Human_Splice_Rec_1594761,Human_Splice_Rec_1594767,Human_Splice_Rec_1594773,Human_Splice_Rec_1594777,Human_Splice_Rec_1594781,Human_Splice_Rec_1594793,Human_Splice_Rec_1594805,Human_Splice_Rec_1594809,Human_Splice_Rec_1594813,Human_Splice_Rec_1594815 RMVar_hsa_circ_91551,RMVar_hsa_circ_374696,RMVar_hsa_circ_171547,RMVar_hsa_circ_171548 61883 RMVar_ID_61883 Human_SNP_ID_575309656 m1A Human chr15 + 43793613 43793613 43793613 GAGTACAGCAGCCAAACGCTGAACTTAGTCCCATCCACTTCCATCTTATCCTTTGTGCCCTTCAT GAGTACAGCAGCCAAACGCTGAACTTAGTCCCGTCCACTTCCATCTTATCCTTTGTGCCCTTCAT A G SERF2 Ensembl:ENSG00000140264 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:43793610..43793775 26863196 MeRIP-seq:(Medium) rs1284635149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1594758 RMVar_hsa_circ_91551,RMVar_hsa_circ_374696,RMVar_hsa_circ_171547,RMVar_hsa_circ_171548 61884 RMVar_ID_61884 Human_SNP_ID_575309677 m1A Human chr15 - 43793645 43793645 43793645 ACCAGAGGGCAAAAAGGACAAGATGCAGGGGGATGAAGGGCACAAAGGATAAGATGGAAGTGGAT ACCAGAGGGCAAAAAGGACAAGATGCAGGGGGTTGAAGGGCACAAAGGATAAGATGGAAGTGGAT T A AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43793642..43794000 26863196 MeRIP-seq:(Medium) rs1298847802 Functional Loss SNV dbSNP153 33..33 33 - - - 61885 RMVar_ID_61885 Human_SNP_ID_575309697 m1A Human chr15 + 43793678 43793678 43793678 CCCCCTGCATCTTGTCCTTTTTGCCCTCTGGTACCTCCCAGTGCCCCATCATCTCTACCCCCAGG CCCCCTGCATCTTGTCCTTTTTGCCCTCTGGTTCCTCCCAGTGCCCCATCATCTCTACCCCCAGG A T SERF2 Ensembl:ENSG00000140264 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr15:43793676..43794025;chr15:43793676..43793975 26863196,32194978 MeRIP-seq:(Medium) rs1323669467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457717,Human_RBP_ID_20023433 RMVar_hsa_circ_91551,RMVar_hsa_circ_374696,RMVar_hsa_circ_171547,RMVar_hsa_circ_171548 61886 RMVar_ID_61886 Human_SNP_ID_575309762 m1A Human chr15 + 43793832 43793832 43793832 TGCCCTTCGCCTGTGTGCCTGGAGCCAGTCCCACCACGCTCGCGTTTCCTCCTGTAGTGCTCACA TGCCCTTCGCCTGTGTGCCTGGAGCCAGTCCCGCCACGCTCGCGTTTCCTCCTGTAGTGCTCACA A G SERF2 Ensembl:ENSG00000140264 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:43793612..43793927 26863196 MeRIP-seq:(Medium) rs1415942574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457719,Human_RBP_ID_758961,Human_RBP_ID_1000699,Human_RBP_ID_1087876,Human_RBP_ID_1174561,Human_RBP_ID_1829587,Human_RBP_ID_4322811,Human_RBP_ID_6427497,Human_RBP_ID_8416934,Human_RBP_ID_9324249,Human_RBP_ID_12513363,Human_RBP_ID_17651822,Human_RBP_ID_18436441,Human_RBP_ID_18662985,Human_RBP_ID_18938153,Human_RBP_ID_22191431,Human_RBP_ID_22439772,Human_RBP_ID_23652402,Human_RBP_ID_26931641 Human_miRNA_ID_1702280,Human_miRNA_ID_3078294 RMVar_hsa_circ_91551,RMVar_hsa_circ_374696,RMVar_hsa_circ_171547,RMVar_hsa_circ_171548 61887 RMVar_ID_61887 Human_SNP_ID_575309780 m1A Human chr15 - 43793854 43793854 43793854 GAATGCCATCGGTGCTGGGACCTGTGAGCACTACAGGAGGAAACGCGAGCGTGGTGGGACTGGCT GAATGCCATCGGTGCTGGGACCTGTGAGCACTGCAGGAGGAAACGCGAGCGTGGTGGGACTGGCT T C AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:43793815..43793930 26863196 MeRIP-seq:(Medium) rs765520151 Functional Loss SNV dbSNP153 33..33 33 - - - 61888 RMVar_ID_61888 Human_SNP_ID_575310201 m1A Human chr15 + 43795034 43795034 43795034 AGACTGGAGGATATTTGTTATCTGGGGATATGATGCGGTGGCGGCGGCGCCTCAAGATAAGGGGC AGACTGGAGGATATTTGTTATCTGGGGATATGGTGCGGTGGCGGCGGCGCCTCAAGATAAGGGGC A G SERF2 Ensembl:ENSG00000140264 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43794983..43795050 26863196 MeRIP-seq:(Medium) rs1186591979 Functional Loss SNV dbSNP153 33..33 33 - - - 61889 RMVar_ID_61889 Human_SNP_ID_575312345 m1A Human chr15 - 43800661 43800660 43800662 TTCTCCGGAGGCCGCTCTGGTCCACTGGTCTCAGTCTCCAACTCCAGCTCCACATCCCCCTCGGT TTCTCCGGAGGCCGCTCTGGTCCACTGGTCT__GTCTCCAACTCCAGCTCCACATCCCCCTCGGT CTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43800576..43801804 26863196 MeRIP-seq:(Medium) rs774320585 Functional Loss DEL dbSNP153 32..33 33 - - - 61890 RMVar_ID_61890 Human_SNP_ID_575312347 m1A Human chr15 - 43800661 43800661 43800661 TTCTCCGGAGGCCGCTCTGGTCCACTGGTCTCAGTCTCCAACTCCAGCTCCACATCCCCCTCGGT TTCTCCGGAGGCCGCTCTGGTCCACTGGTCTCCGTCTCCAACTCCAGCTCCACATCCCCCTCGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43800576..43801804 26863196 MeRIP-seq:(Medium) rs1189454705 Functional Loss SNV dbSNP153 33..33 33 - - - 61891 RMVar_ID_61891 Human_SNP_ID_575312369 m1A Human chr15 + 43800703 43800703 43800703 GGACCAGAGCGGCCTCCGGAGAAGCCACGGAAACATGACAGCGGTGCGGCGGACTTGGAGCGGGT GGACCAGAGCGGCCTCCGGAGAAGCCACGGAAGCATGACAGCGGTGCGGCGGACTTGGAGCGGGT A G SERF2,HYPK Ensembl:ENSG00000140264,Ensembl:ENSG00000242028 Protein coding,Protein coding 3'UTR,CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:43800601..43800800 26863410 MeRIP-seq:(Medium) rs1213034700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4345073,Human_RBP_ID_9052385,Human_RBP_ID_9370826,Human_RBP_ID_17652128,Human_RBP_ID_20090784,Human_RBP_ID_22928777,Human_RBP_ID_26326623,Human_RBP_ID_26931646 Human_Splice_Rec_1594785,Human_Splice_Rec_1594795,Human_Splice_Rec_1594911,Human_Splice_Rec_1594917,Human_Splice_Rec_1594919,Human_Splice_Rec_1594925,Human_Splice_Rec_1594927 61892 RMVar_ID_61892 Human_SNP_ID_575315002 m1A Human chr15 + 43809869 43809869 43809869 TTTGCCCGAAGTTCAGCTCTCCTCTCTTCCTCAGTCAGGTTTCGCATGCGTTCAATTTCTGCTTT TTTGCCCGAAGTTCAGCTCTCCTCTCTTCCTCCGTCAGGTTTCGCATGCGTTCAATTTCTGCTTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:43809818..43809977 26863196 MeRIP-seq:(Medium) rs937090420 Functional Loss SNV dbSNP153 33..33 33 - - - 61893 RMVar_ID_61893 Human_SNP_ID_575315006 m1A Human chr15 + 43809882 43809882 43809882 CAGCTCTCCTCTCTTCCTCAGTCAGGTTTCGCATGCGTTCAATTTCTGCTTTCTCCTTCTCAAGC CAGCTCTCCTCTCTTCCTCAGTCAGGTTTCGCGTGCGTTCAATTTCTGCTTTCTCCTTCTCAAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43809831..43809964 26863196 MeRIP-seq:(Medium) rs770189123 Functional Loss SNV dbSNP153 33..33 33 - - - 61894 RMVar_ID_61894 Human_SNP_ID_575316322 m1A Human chr15 - 43814685 43814685 43814685 CTGACTGGCTTATATATATGACTTGATAGGAAATAGAGCGGCGGCGTGGCATGATGCGTCAGCGA CTGACTGGCTTATATATATGACTTGATAGGAAGTAGAGCGGCGGCGTGGCATGATGCGTCAGCGA T C MFAP1 Ensembl:ENSG00000140259 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:43814563..43814737;chr15:43814509..43824674 26863196 MeRIP-seq:(Medium) rs777681279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1511583,Human_RBP_ID_24544063,Human_RBP_ID_26326633,Human_RBP_ID_27809446 Human_Splice_Rec_1594936 RMVar_hsa_circ_123979,RMVar_hsa_circ_3164,RMVar_hsa_circ_378570,RMVar_hsa_circ_360176,RMVar_hsa_circ_171549 61895 RMVar_ID_61895 Human_SNP_ID_575316904 m1A Human chr15 - 43817182 43817182 43817182 TGTGTTTACTTGAACATGAACCTCTACAGCTTAATAATAATAATAATAGCTAATACTTGAATAGT TGTGTTTACTTGAACATGAACCTCTACAGCTTGATAATAATAATAATAGCTAATACTTGAATAGT T C MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43817180..43817272 26863196 MeRIP-seq:(Medium) rs376162441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123979,RMVar_hsa_circ_3164,RMVar_hsa_circ_171549 61896 RMVar_ID_61896 Human_SNP_ID_575319627 m1A Human chr15 - 43827042 43827042 43827042 TCTGGAGTCCGCCTTCTCAGCCGCCGCGCCCGACCTGGACATCTTTCGGCTTCTTAGCGGCCGGC TCTGGAGTCCGCCTTCTCAGCCGCCGCGCCCGCCCTGGACATCTTTCGGCTTCTTAGCGGCCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43827001..43827115 26863196 MeRIP-seq:(Medium) rs745565950 Functional Loss SNV dbSNP153 33..33 33 - - - 61897 RMVar_ID_61897 Human_SNP_ID_575319647 m1A Human chr15 + 43827076 43827076 43827076 GGGCGCGGCGGCTGAGAAGGCGGACTCCAGACAGCGACCCCAGATGAAGGTGAGAAACGGACTGG GGGCGCGGCGGCTGAGAAGGCGGACTCCAGACGGCGACCCCAGATGAAGGTGAGAAACGGACTGG A G WDR76 Ensembl:ENSG00000092470 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:43827001..43827153 26863196 MeRIP-seq:(Medium) rs1273781405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342638,Human_RBP_ID_9283635,Human_RBP_ID_12513695,Human_RBP_ID_18663016 Human_Splice_Rec_1594951,Human_Splice_Rec_1594975,Human_Splice_Rec_1594987 61898 RMVar_ID_61898 Human_SNP_ID_575319911 m1A Human chr15 - 43827937 43827937 43827937 TTTACCTATTCAGATCAATAAAAGAAAACAGAATATTAGAACTCCAAGTCCTGTGCCTTTTCTTA TTTACCTATTCAGATCAATAAAAGAAAACAGAGTATTAGAACTCCAAGTCCTGTGCCTTTTCTTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:43827935..43828061 26863196 MeRIP-seq:(Medium) rs1212411627 Functional Loss SNV dbSNP153 33..33 33 - - - 61899 RMVar_ID_61899 Human_SNP_ID_575325367 m1A Human chr15 + 43846053 43846053 43846053 AACTGAAGCAAAAAAGTGGGAAGAAGATCAGAATAGTATGTTTTGGAAGCCAAGAGATGAGTTTC AACTGAAGCAAAAAAGTGGGAAGAAGATCAGAGTAGTATGTTTTGGAAGCCAAGAGATGAGTTTC A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43846047..43846283 26863196 MeRIP-seq:(Medium) rs989884142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54266,RMVar_hsa_circ_316575,RMVar_hsa_circ_171550,RMVar_hsa_circ_50141,RMVar_hsa_circ_85971,RMVar_hsa_circ_324238,RMVar_hsa_circ_348003,RMVar_hsa_circ_171555,RMVar_hsa_circ_171554,RMVar_hsa_circ_43869,RMVar_hsa_circ_31960 61900 RMVar_ID_61900 Human_SNP_ID_575434942 m1A Human chr15 - 44288813 44288813 44288813 CCCTCCTCAAATCAGGCCAAAACGCGTTCCGGAGGCTTTGAACCCGACCCTGCACCTGCCCAAGG CCCTCCTCAAATCAGGCCAAAACGCGTTCCGGGGGCTTTGAACCCGACCCTGCACCTGCCCAAGG T C lnc-FRMD5-1,lnc-FRMD5-1:2 RNACentral:URS00008C113C,RNACentral:URS00008BBD75 lincRNA,lincRNA exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:44288773..44288905 26863196 MeRIP-seq:(Medium) rs530948457 Functional Loss SNV dbSNP153 33..33 33 - - - 61901 RMVar_ID_61901 Human_SNP_ID_575435110 m1A Human chr15 + 44289259 44289259 44289259 CAATTCGGACCTCTTGCTGTTGGTGGACACGCACAAGAAACAGATCGACCAGAAGGAGGCCGACT CAATTCGGACCTCTTGCTGTTGGTGGACACGCGCAAGAAACAGATCGACCAGAAGGAGGCCGACT A G CASC4 Ensembl:ENSG00000166734 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:44289208..44289309 26863196 MeRIP-seq:(Medium) rs1368570428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1595257,Human_Splice_Rec_1595277,Human_Splice_Rec_1595285,Human_Splice_Rec_1595297,Human_Splice_Rec_1595317,Human_Splice_Rec_1595319,Human_Splice_Rec_1595335 Human_miRNA_ID_577196 61902 RMVar_ID_61902 Human_SNP_ID_575441358 m1A Human chr15 + 44315583 44315582 44315583 AGATTAAGGGAAAATAAATGAAGTAGCTGGGGATGAACAAGAAGTACTATAGGGAAGTATCAGGA AGATTAAGGGAAAATAAATGAAGTAGCTGGGG_TGAACAAGAAGTACTATAGGGAAGTATCAGGA GA G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:44315579..44315648 26863196 MeRIP-seq:(Medium) rs1162036982 Functional Loss DEL dbSNP153 33..33 33 - - - 61903 RMVar_ID_61903 Human_SNP_ID_575441493 m1A Human chr15 + 44316279 44316279 44316279 AGAGCTGGGTGTGGTGGCCTGAGCCTGTTGTCACAGCTACTGAGTTCGAGTTCAGCCTGGGCAAC AGAGCTGGGTGTGGTGGCCTGAGCCTGTTGTCGCAGCTACTGAGTTCGAGTTCAGCCTGGGCAAC A G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:44316277..44316419 26863196 MeRIP-seq:(Medium) rs978433990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5179378 61904 RMVar_ID_61904 Human_SNP_ID_575468334 m1A Human chr15 + 44427666 44427666 44427666 AGGTCGGTAGGCGGGAAATGGCGACTGGCTGAAGGAGCTGGTTCTGTTGCTGCTGCGGGGTAAGC AGGTCGGTAGGCGGGAAATGGCGACTGGCTGAGGGAGCTGGTTCTGTTGCTGCTGCGGGGTAAGC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:44427601..44427832 26863196 MeRIP-seq:(Medium) rs1362914961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759476,Human_RBP_ID_4323078,Human_RBP_ID_6428653,Human_RBP_ID_9370839,Human_RBP_ID_12515993,Human_RBP_ID_18418351,Human_RBP_ID_26326646,Human_RBP_ID_27810210 Human_Splice_Rec_1595367 61905 RMVar_ID_61905 Human_SNP_ID_575468345 m1A Human chr15 + 44427704 44427704 44427704 TGGTTCTGTTGCTGCTGCGGGGTAAGCGGGAAAGACACCACACATTGCGCAGTCGGGACCATCGC TGGTTCTGTTGCTGCTGCGGGGTAAGCGGGAAGGACACCACACATTGCGCAGTCGGGACCATCGC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:44427654..44427814 26863196 MeRIP-seq:(Medium) rs936367612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41435,Human_RBP_ID_4342642,Human_RBP_ID_5141488,Human_RBP_ID_9370839,Human_RBP_ID_18418351,Human_RBP_ID_22440566,Human_RBP_ID_26326646,Human_RBP_ID_27810210 Human_Splice_Rec_1595375,Human_Splice_Rec_1595399 61906 RMVar_ID_61906 Human_SNP_ID_575477129 m1A Human chr15 - 44459048 44459048 44459048 TCTGGCAGTGCGTTGTGTTTGGATTTGATTTGACTGCTGAGAAGCTTTCCGTGTTCTCAGCCTCA TCTGGCAGTGCGTTGTGTTTGGATTTGATTTGGCTGCTGAGAAGCTTTCCGTGTTCTCAGCCTCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:44458942..44459074 26863196 MeRIP-seq:(Medium) rs767261009 Functional Loss SNV dbSNP153 33..33 33 - - - 61907 RMVar_ID_61907 Human_SNP_ID_575477130 m1A Human chr15 + 44459051 44459051 44459051 GGCTGAGAACACGGAAAGCTTCTCAGCAGTCAAATCAAATCCAAACACAACGCACTGCCAGAGCA GGCTGAGAACACGGAAAGCTTCTCAGCAGTCAGATCAAATCCAAACACAACGCACTGCCAGAGCA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:44458961..44459082 26863196 MeRIP-seq:(Medium) rs368247562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1000742,Human_RBP_ID_9282994,Human_RBP_ID_17249981,Human_RBP_ID_17365248,Human_RBP_ID_17482187,Human_RBP_ID_17860811,Human_RBP_ID_26326648 Human_Splice_Rec_1595368,Human_Splice_Rec_1595376,Human_Splice_Rec_1595400,Human_Splice_Rec_1595406,Human_Splice_Rec_1595430,Human_Splice_Rec_1595436 RMVar_hsa_circ_69757,RMVar_hsa_circ_171584,RMVar_hsa_circ_92000,RMVar_hsa_circ_303487,RMVar_hsa_circ_354023,RMVar_hsa_circ_327814,RMVar_hsa_circ_278698,RMVar_hsa_circ_171587,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_12303,RMVar_hsa_circ_171588,RMVar_hsa_circ_171586 61908 RMVar_ID_61908 Human_SNP_ID_575501067 m1A Human chr15 + 44550813 44550813 44550813 CAACAAACATTTCTCTGGAGTTAGTCAAGTTGATAATAAAGTTCACATAGAAAAGCAAACATGCA CAACAAACATTTCTCTGGAGTTAGTCAAGTTGTTAATAAAGTTCACATAGAAAAGCAAACATGCA A T EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:44550810..44557550 26863196 MeRIP-seq:(Medium) rs974681607 Functional Loss SNV dbSNP153 33..33 33 - - - 61909 RMVar_ID_61909 Human_SNP_ID_575501254 m1A Human chr15 + 44551480 44551480 44551480 AAGAAAAAAATAGCAGAGAAGATAAAAGAGAAAGAACGGCAACAGAAGAAAAGGCAAGAAGAAAT AAGAAAAAAATAGCAGAGAAGATAAAAGAGAAGGAACGGCAACAGAAGAAAAGGCAAGAAGAAAT A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:44551386..44551560 26863196 MeRIP-seq:(Medium) rs1314751609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43079,Human_RBP_ID_1511590,Human_RBP_ID_2441749,Human_RBP_ID_5566410,Human_RBP_ID_9370847,Human_RBP_ID_23113785,Human_RBP_ID_24544066,Human_RBP_ID_26326658,Human_RBP_ID_27809467 Human_Splice_Rec_1595522,Human_Splice_Rec_1595523,Human_Splice_Rec_1595536,Human_Splice_Rec_1595537,Human_Splice_Rec_1595544,Human_Splice_Rec_1595545,Human_Splice_Rec_1595547 RMVar_hsa_circ_30737,RMVar_hsa_circ_300962,RMVar_hsa_circ_332229,RMVar_hsa_circ_281284,RMVar_hsa_circ_171609 61910 RMVar_ID_61910 Human_SNP_ID_575502114 m1A Human chr15 + 44554510 44554510 44554510 GAATTCGTACAATACAGAAAGGTACTGAGTGCATCATAATCCCTGTGCTTTTTAAAAACTTTTGT GAATTCGTACAATACAGAAAGGTACTGAGTGCCTCATAATCCCTGTGCTTTTTAAAAACTTTTGT A C EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:44554508..44554650 26863196 MeRIP-seq:(Medium) rs1160869796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30737,RMVar_hsa_circ_300962,RMVar_hsa_circ_332229,RMVar_hsa_circ_171609 61911 RMVar_ID_61911 Human_SNP_ID_575532898 m1A Human chr15 + 44663614 44663614 44663614 CATGGCCGCGGTGCCCCAGCTACCGCCGGCGGAAGCAGCACTCGCGACCCCTTCCTCTGCAGCCA CATGGCCGCGGTGCCCCAGCTACCGCCGGCGGGAGCAGCACTCGCGACCCCTTCCTCTGCAGCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:44663551..44663640 26863196 MeRIP-seq:(Medium) rs753871631 Functional Loss SNV dbSNP153 33..33 33 - - - 61912 RMVar_ID_61912 Human_SNP_ID_575544331 m1A Human chr15 + 44711582 44711582 44711582 TCTCGCTCCGTGGCCTTAGCTGTGCTCGCGCTACTCTCTCTTTCTGGCCTGGAGGCTATCCAGCG TCTCGCTCCGTGGCCTTAGCTGTGCTCGCGCTGCTCTCTCTTTCTGGCCTGGAGGCTATCCAGCG A G B2M Ensembl:ENSG00000166710 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:44711501..44711679;chr15:44711501..44711664 26863196 MeRIP-seq:(Medium) rs11553044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42487,Human_RBP_ID_232273,Human_RBP_ID_298354,Human_RBP_ID_458100,Human_RBP_ID_759128,Human_RBP_ID_815149,Human_RBP_ID_887565,Human_RBP_ID_1000773,Human_RBP_ID_1504960,Human_RBP_ID_3475157,Human_RBP_ID_4323350,Human_RBP_ID_5316071,Human_RBP_ID_5494390,Human_RBP_ID_6429621,Human_RBP_ID_8417302,Human_RBP_ID_9324257,Human_RBP_ID_17187745,Human_RBP_ID_17482241,Human_RBP_ID_18663312,Human_RBP_ID_20003791,Human_RBP_ID_22439776,Human_RBP_ID_22759583,Human_RBP_ID_23653066,Human_RBP_ID_24473603,Human_RBP_ID_25142108,Human_RBP_ID_26931775,Human_RBP_ID_27435378,Human_RBP_ID_27559415 Human_Splice_Rec_1596093,Human_Splice_Rec_1596097,Human_Splice_Rec_1596103,Human_Splice_Rec_1596111,Human_Splice_Rec_1596119,Human_Splice_Rec_1596125 RMVar_hsa_circ_171696,RMVar_hsa_circ_121594 61913 RMVar_ID_61913 Human_SNP_ID_575544332 m1A Human chr15 + 44711582 44711582 44711582 TCTCGCTCCGTGGCCTTAGCTGTGCTCGCGCTACTCTCTCTTTCTGGCCTGGAGGCTATCCAGCG TCTCGCTCCGTGGCCTTAGCTGTGCTCGCGCTTCTCTCTCTTTCTGGCCTGGAGGCTATCCAGCG A T B2M Ensembl:ENSG00000166710 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:44711501..44711679;chr15:44711501..44711664 26863196 MeRIP-seq:(Medium) rs11553044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42487,Human_RBP_ID_232273,Human_RBP_ID_298354,Human_RBP_ID_458100,Human_RBP_ID_759128,Human_RBP_ID_815149,Human_RBP_ID_887565,Human_RBP_ID_1000773,Human_RBP_ID_1504960,Human_RBP_ID_3475157,Human_RBP_ID_4323350,Human_RBP_ID_5316071,Human_RBP_ID_5494390,Human_RBP_ID_6429621,Human_RBP_ID_8417302,Human_RBP_ID_9324257,Human_RBP_ID_17187745,Human_RBP_ID_17482241,Human_RBP_ID_18663312,Human_RBP_ID_20003791,Human_RBP_ID_22439776,Human_RBP_ID_22759583,Human_RBP_ID_23653066,Human_RBP_ID_24473603,Human_RBP_ID_25142108,Human_RBP_ID_26931775,Human_RBP_ID_27435378,Human_RBP_ID_27559415 Human_Splice_Rec_1596093,Human_Splice_Rec_1596097,Human_Splice_Rec_1596103,Human_Splice_Rec_1596111,Human_Splice_Rec_1596119,Human_Splice_Rec_1596125 RMVar_hsa_circ_171696,RMVar_hsa_circ_121594 61914 RMVar_ID_61914 Human_SNP_ID_575544345 m1A Human chr15 + 44711611 44711611 44711611 GCTACTCTCTCTTTCTGGCCTGGAGGCTATCCAGCGTGAGTCTCTCCTACCCTCCCGCTCTGGTC GCTACTCTCTCTTTCTGGCCTGGAGGCTATCCGGCGTGAGTCTCTCCTACCCTCCCGCTCTGGTC A G B2M Ensembl:ENSG00000166710 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:44711526..44711625 26863410 MeRIP-seq:(Medium) rs1213728428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232273,Human_RBP_ID_458101,Human_RBP_ID_759128,Human_RBP_ID_815149,Human_RBP_ID_887565,Human_RBP_ID_3475157,Human_RBP_ID_4342270,Human_RBP_ID_5316071,Human_RBP_ID_9324257,Human_RBP_ID_22439776,Human_RBP_ID_22759043,Human_RBP_ID_27435378 Human_Splice_Rec_1596093,Human_Splice_Rec_1596097,Human_Splice_Rec_1596103,Human_Splice_Rec_1596111,Human_Splice_Rec_1596119,Human_Splice_Rec_1596125 RMVar_hsa_circ_171696,RMVar_hsa_circ_121594 61915 RMVar_ID_61915 Human_SNP_ID_575544412 m1A Human chr15 - 44711798 44711798 44711798 AAAGGGGCAAGTAGCGCGCGTCCCGGGTGCGCACCCCCTTCCCCACTCCCAGGCCACCCCGCCGC AAAGGGGCAAGTAGCGCGCGTCCCGGGTGCGCCCCCCCTTCCCCACTCCCAGGCCACCCCGCCGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:44711794..44712035 26863196 MeRIP-seq:(Medium) rs1013755482 Functional Loss SNV dbSNP153 33..33 33 - - - 61916 RMVar_ID_61916 Human_SNP_ID_575545242 m1A Human chr15 - 44715381 44715381 44715381 ATCGGGAAAAGACACATTAATATTGCCAGGGTATTTCACTTGGGGCTAACTTGGTGTCAAGCTAT ATCGGGAAAAGACACATTAATATTGCCAGGGTGTTTCACTTGGGGCTAACTTGGTGTCAAGCTAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:44715378..44715710 26863196 MeRIP-seq:(Medium) rs766655028 Functional Loss SNV dbSNP153 33..33 33 - - - 61917 RMVar_ID_61917 Human_SNP_ID_575545274 m1A Human chr15 + 44715469 44715469 44715469 CAGGTTTACTCACGTCATCCAGCAGAGAATGGAAAGTCAAATTTCCTGAATTGCTATGTGTCTGG CAGGTTTACTCACGTCATCCAGCAGAGAATGGGAAGTCAAATTTCCTGAATTGCTATGTGTCTGG A G B2M Ensembl:ENSG00000166710 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1455449641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_458105,Human_RBP_ID_1829891,Human_RBP_ID_3475160,Human_RBP_ID_4342650,Human_RBP_ID_22387955,Human_RBP_ID_22439778,Human_RBP_ID_22758794,Human_RBP_ID_26808879 Human_Splice_Rec_1596094,Human_Splice_Rec_1596098,Human_Splice_Rec_1596104,Human_Splice_Rec_1596112,Human_Splice_Rec_1596120,Human_Splice_Rec_1596126,Human_Splice_Rec_1596132,Human_Splice_Rec_1596138 Human_miRNA_ID_2765805 RMVar_hsa_circ_171696,RMVar_hsa_circ_121594,RMVar_hsa_circ_69743 61918 RMVar_ID_61918 Human_SNP_ID_575545299 m1A Human chr15 - 44715552 44715552 44715552 TGAAAGACAAGTCTGAATGCTCCACTTTTTCAATTCTCTCTCCATTCTTCAGTAAGTCAACTTCA TGAAAGACAAGTCTGAATGCTCCACTTTTTCAGTTCTCTCTCCATTCTTCAGTAAGTCAACTTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:44715401..44715700 32194978 MeRIP-seq:(Medium) rs928269033 Functional Loss SNV dbSNP153 33..33 33 - - - 61919 RMVar_ID_61919 Human_SNP_ID_695536645 m1A Human chr21 + 41150716 41150716 41150716 GTGTAGTGTGGTGTGGTAAGGGAGTGTATATGATGTGTGTGCGGTATGCAATGTGTGTGTCTGAG GTGTAGTGTGGTGTGGTAAGGGAGTGTATATGCTGTGTGTGCGGTATGCAATGTGTGTGTCTGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41150665..41150761 26863196 MeRIP-seq:(Medium) rs1278116911 Functional Loss SNV dbSNP153 33..33 33 - - - 61920 RMVar_ID_61920 Human_SNP_ID_695540954 m1A Human chr21 - 41168316 41168316 41168316 AGGGCGCGGGGGCCAGCTCCGGGGCGGCGCGCAGGAGCCACTGGGCCAGCAGAGGCAGCAGCAGC AGGGCGCGGGGGCCAGCTCCGGGGCGGCGCGCGGGAGCCACTGGGCCAGCAGAGGCAGCAGCAGC T C LINC00323,LINC00323:2,LINC00323:3,LINC00323:4,LINC00323:5 RNACentral:URS0000D6D973,RNACentral:URS0000D5ACD3,RNACentral:URS0000D5CBF8,RNACentral:URS0000D59587,RNACentral:URS0000D6E020 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41167847..41168403 26863196 MeRIP-seq:(Medium) rs190721616 Functional Loss SNV dbSNP153 33..33 33 - - - 61921 RMVar_ID_61921 Human_SNP_ID_695543820 m1A Human chr21 - 41179295 41179273 41179295 CCTGGACACTCTCACTCACCCTGACACCCTCAATCCTCACCCTGGACTCCCTCACTCCTCACCCT CCTGGACACTCTCACTCACCCTGACACCCTCA______________________CTCCTCACCCT GTGAGGGAGTCCAGGGTGAGGAT G PLAC4 Ensembl:ENSG00000280109 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41178999..41179590 26863196 MeRIP-seq:(Medium) rs747303577 Functional Loss DEL dbSNP153 33..54 33 - - - 61922 RMVar_ID_61922 Human_SNP_ID_695543830 m1A Human chr21 - 41179295 41179295 41179295 CCTGGACACTCTCACTCACCCTGACACCCTCAATCCTCACCCTGGACTCCCTCACTCCTCACCCT CCTGGACACTCTCACTCACCCTGACACCCTCACTCCTCACCCTGGACTCCCTCACTCCTCACCCT T G PLAC4 Ensembl:ENSG00000280109 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41178999..41179590 26863196 MeRIP-seq:(Medium) rs200016409 Functional Loss SNV dbSNP153 33..33 33 - - - 61923 RMVar_ID_61923 Human_SNP_ID_695543840 m1A Human chr21 + 41179318 41179318 41179318 GGGTGAGGATTGAGGGTGTCAGGGTGAGTGAGAGTGTCCAGGGTGAGGAGTGAGGGTATCCAGGG GGGTGAGGATTGAGGGTGTCAGGGTGAGTGAGGGTGTCCAGGGTGAGGAGTGAGGGTATCCAGGG A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:41179301..41179550 26863196 MeRIP-seq:(Medium) rs200941231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23928079 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61924 RMVar_ID_61924 Human_SNP_ID_695543920 m1A Human chr21 + 41179472 41179472 41179472 GTCCAGGGTGAGTGAGGGTGTCCAGGGTGCAGAGTGAGGTGTCCAGGGTGAGGAGTGACGGTGTC GTCCAGGGTGAGTGAGGGTGTCCAGGGTGCAGCGTGAGGTGTCCAGGGTGAGGAGTGACGGTGTC A C BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:41178894..41179663;chr21:41178772..41179675 26863196 MeRIP-seq:(Medium) rs367746564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10038536,Human_RBP_ID_23928081 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61925 RMVar_ID_61925 Human_SNP_ID_695549483 m1A Human chr21 + 41203378 41203378 41203378 TGCTTGGGGAAGGGTGTCCAGGCAGAAGGAAGAGCCAGTACGACGGCCTTGAGGAGGAGCTGTGC TGCTTGGGGAAGGGTGTCCAGGCAGAAGGAAGTGCCAGTACGACGGCCTTGAGGAGGAGCTGTGC A T BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:41203301..41203550 26863196 MeRIP-seq:(Medium) rs1489123971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61926 RMVar_ID_61926 Human_SNP_ID_695549598 m1A Human chr21 + 41203876 41203876 41203876 GTTTTGAAAGACGTCAAACCCCTCAGCAGGTCAGCCGTGGCTGGAGAGGACATTGCTACAGAGAG GTTTTGAAAGACGTCAAACCCCTCAGCAGGTCCGCCGTGGCTGGAGAGGACATTGCTACAGAGAG A C BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:41203708..41203975;chr21:41203676..41204025 26863196 MeRIP-seq:(Medium) rs1467600102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14313089 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61927 RMVar_ID_61927 Human_SNP_ID_695551728 m1A Human chr21 + 41213116 41213116 41213116 CATCTGAAGGAACAAGTGATTAGTGAATTCCTATTAGTTGCAGGCACTGTGGGGACCATCAAAAA CATCTGAAGGAACAAGTGATTAGTGAATTCCTGTTAGTTGCAGGCACTGTGGGGACCATCAAAAA A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41213113..41213217 26863196 MeRIP-seq:(Medium) rs1336735183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2704503,Human_RBP_ID_14313205 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61928 RMVar_ID_61928 Human_SNP_ID_695552182 m1A Human chr21 + 41215061 41215061 41215061 GCCTGCAGGCTGGACAGGTCAGGGGAGAGCTCAGAGATGACCGTGGGCCTGGAGCACGGGAGGTC GCCTGCAGGCTGGACAGGTCAGGGGAGAGCTCCGAGATGACCGTGGGCCTGGAGCACGGGAGGTC A C BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41215050..41215184 26863196 MeRIP-seq:(Medium) rs1358636646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14313239 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61929 RMVar_ID_61929 Human_SNP_ID_695552185 m1A Human chr21 + 41215065 41215065 41215065 GCAGGCTGGACAGGTCAGGGGAGAGCTCAGAGATGACCGTGGGCCTGGAGCACGGGAGGTCACTG GCAGGCTGGACAGGTCAGGGGAGAGCTCAGAGGTGACCGTGGGCCTGGAGCACGGGAGGTCACTG A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:41214810..41215225 26863196 MeRIP-seq:(Medium) rs902905108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14313239 RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 61930 RMVar_ID_61930 Human_SNP_ID_695554508 m1A Human chr21 - 41223908 41223908 41223908 CTCAGCTCAGGAATCACTTCTGGGATCCATCCACTCACACCCTTGGGGTCCCCACTGAGTCTCAA CTCAGCTCAGGAATCACTTCTGGGATCCATCCGCTCACACCCTTGGGGTCCCCACTGAGTCTCAA T C LINC00323,LINC00323:2 RNACentral:URS0000D6D973,RNACentral:URS0000D6E020 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41223901..41224064 26863196 MeRIP-seq:(Medium) rs1424975445 Functional Loss SNV dbSNP153 33..33 33 - - - 61931 RMVar_ID_61931 Human_SNP_ID_695557578 m1A Human chr21 - 41236652 41236652 41236652 AAATAATGACCAAGCCCTACCTGCTGAAGCCCAGGTCCTTCATGTCACAGGTCCTTCTCAAGGTT AAATAATGACCAAGCCCTACCTGCTGAAGCCCTGGTCCTTCATGTCACAGGTCCTTCTCAAGGTT T A LINC00323,LINC00323:2 RNACentral:URS0000D6D973,RNACentral:URS0000D6E020 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41236649..41236799 26863196 MeRIP-seq:(Medium) rs1307061752 Functional Loss SNV dbSNP153 33..33 33 - - - 61932 RMVar_ID_61932 Human_SNP_ID_695562363 m1A Human chr21 + 41255333 41255333 41255333 CACGGGGTGACCTAGGGCCATGGGGTGGGGCCAGATGGGTCACCCAAGGAGGGAAGATTGAGAGG CACGGGGTGACCTAGGGCCATGGGGTGGGGCCGGATGGGTCACCCAAGGAGGGAAGATTGAGAGG A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:41255322..41255462 26863196 MeRIP-seq:(Medium) rs985295988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_298531,RMVar_hsa_circ_212364,RMVar_hsa_circ_292343,RMVar_hsa_circ_212366,RMVar_hsa_circ_212368,RMVar_hsa_circ_375837,RMVar_hsa_circ_42997,RMVar_hsa_circ_212371,RMVar_hsa_circ_322940 61933 RMVar_ID_61933 Human_SNP_ID_695566865 m1A Human chr21 - 41275533 41275531 41275534 GGCGACGCTGACACCGGAACGGCAGCAGCAGCAGGACGATTAAGACAAGGAGGATGGCTCCACAG GGCGACGCTGACACCGGAACGGCAGCAGCAG___GACGATTAAGACAAGGAGGATGGCTCCACAG CCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr21:41275351..41275656;chr21:41275482..41275625 26863196 MeRIP-seq:(Medium) rs759116061 Functional Loss DEL dbSNP153 32..34 33 - - - 61934 RMVar_ID_61934 Human_SNP_ID_695566871 m1A Human chr21 - 41275542 41275542 41275542 GGTCACGGGGGCGACGCTGACACCGGAACGGCAGCAGCAGCAGGACGATTAAGACAAGGAGGATG GGTCACGGGGGCGACGCTGACACCGGAACGGCGGCAGCAGCAGGACGATTAAGACAAGGAGGATG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:41275526..41275550 26863196 MeRIP-seq:(Medium) rs1429528982 Functional Loss SNV dbSNP153 33..33 33 - - - 61935 RMVar_ID_61935 Human_SNP_ID_695568147 m1A Human chr21 - 41281042 41281042 41281042 CTGGCAGAGACACCAGGATGGCTGCTCTCACAATAGTGTCCAAGAAGTACCCGAGGCTCAACGGG CTGGCAGAGACACCAGGATGGCTGCTCTCACACTAGTGTCCAAGAAGTACCCGAGGCTCAACGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:41280826..41281075 26863196 MeRIP-seq:(Medium) rs1458350033 Functional Loss SNV dbSNP153 33..33 33 - - - 61936 RMVar_ID_61936 Human_SNP_ID_695602610 m1A Human chr21 + 41420669 41420669 41420669 TGCAGGATCCTGAGGCCCGTGTTTGCAGGACCAGGGCCGGCCTTCCGATTCCCCATTCATTCCAG TGCAGGATCCTGAGGCCCGTGTTTGCAGGACCGGGGCCGGCCTTCCGATTCCCCATTCATTCCAG A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41420619..41420690 26863196 MeRIP-seq:(Medium) rs909176415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212377,RMVar_hsa_circ_212379,RMVar_hsa_circ_79996 61937 RMVar_ID_61937 Human_SNP_ID_695697043 m1A Human chr21 + 41767047 41767047 41767047 CCATGGGGTCCCGCCGTCGCCCTCCATCGCGCACGTCTAGCCAGCGCCGCGGCGGCTGCCCAGGT CCATGGGGTCCCGCCGTCGCCCTCCATCGCGCGCGTCTAGCCAGCGCCGCGGCGGCTGCCCAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41766886..41767065 26863196 MeRIP-seq:(Medium) rs1006478324 Functional Loss SNV dbSNP153 33..33 33 - - - 61938 RMVar_ID_61938 Human_SNP_ID_695707857 m1A Human chr21 - 41805930 41805926 41805930 GGTGATGCCACGTGGTGGTAGTGGTACTGATGATGGTGGTGACAGTGTTGGTGGTGATGAGGGTA GGTGATGCCACGTGGTGGTAGTGGTACTGATG____TGGTGACAGTGTTGGTGGTGATGAGGGTA ACCAT A PRDM15 Ensembl:ENSG00000141956 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41805685..41806010 26863196 MeRIP-seq:(Medium) rs1305728673 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_17145998,Human_RBP_ID_23928180 RMVar_hsa_circ_15276 61939 RMVar_ID_61939 Human_SNP_ID_695707861 m1A Human chr21 - 41805933 41805933 41805933 GGTGGTGATGCCACGTGGTGGTAGTGGTACTGATGATGGTGGTGACAGTGTTGGTGGTGATGAGG GGTGGTGATGCCACGTGGTGGTAGTGGTACTGGTGATGGTGGTGACAGTGTTGGTGGTGATGAGG T C PRDM15 Ensembl:ENSG00000141956 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:41805688..41805996 26863196 MeRIP-seq:(Medium) rs894915400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17145998 RMVar_hsa_circ_15276 61940 RMVar_ID_61940 Human_SNP_ID_695712558 m1A Human chr21 + 41819490 41819490 41819490 CGGCCCCCGCCCCCGCCACACCCACCTTCCCCACACTCCCAGTTCTCGCTCATGTCCCCTTCCAG CGGCCCCCGCCCCCGCCACACCCACCTTCCCCCCACTCCCAGTTCTCGCTCATGTCCCCTTCCAG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:41819342..41819623 26863196 MeRIP-seq:(Medium) rs1432612922 Functional Loss SNV dbSNP153 33..33 33 - - - 61941 RMVar_ID_61941 Human_SNP_ID_695713514 m1A Human chr21 + 41822213 41822203 41822213 TTGTGCCCTAGCCCATCCCAGCTTGTCCCCAGAGGTCCCCACCTAAACGCTAAAGCTGCCCTTGC TTGTGCCCTAGCCCATCCCAGCT__________GGTCCCCACCTAAACGCTAAAGCTGCCCTTGC TTGTCCCCAGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41822203..41822293 26863196 MeRIP-seq:(Medium) rs528237151 Functional Loss DEL dbSNP153 24..33 33 - - - 61942 RMVar_ID_61942 Human_SNP_ID_695715958 m1A Human chr21 + 41830142 41830142 41830142 ACACACCACACACAAAAATACACATTCAACACACACCCCACACAAATACACACACAACACACACA ACACACCACACACAAAAATACACATTCAACACGCACCCCACACAAATACACACACAACACACACA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:41830091..41830244 26863196 MeRIP-seq:(Medium) rs1157116163 Functional Loss SNV dbSNP153 33..33 33 - - - 61943 RMVar_ID_61943 Human_SNP_ID_695716036 m1A Human chr21 + 41830349 41830349 41830349 TCAACACATACACCACACACAACCCACACACAAATACACACACAACATACAAACACATACGCTCA TCAACACATACACCACACACAACCCACACACACATACACACACAACATACAAACACATACGCTCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:41830311..41830410 26863196 MeRIP-seq:(Medium) rs1333986018 Functional Loss SNV dbSNP153 33..33 33 - - - 61944 RMVar_ID_61944 Human_SNP_ID_695716092 m1A Human chr21 + 41830557 41830557 41830557 CCACACACGAATACACACAAATCACACATACCACAAATACACTCAACACACACACCACACACCTC CCACACACGAATACACACAAATCACACATACCGCAAATACACTCAACACACACACCACACACCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:41828864..41830741;chr21:41830527..41830718 26863196 MeRIP-seq:(Medium) rs1271329053 Functional Loss SNV dbSNP153 33..33 33 - - - 61945 RMVar_ID_61945 Human_SNP_ID_695716119 m1A Human chr21 + 41830642 41830642 41830642 ACACACAAACACACCACAGAAATACTCAACACACACACCACACAAATACTAAACACACACCACAC ACACACAAACACACCACAGAAATACTCAACACGCACACCACACAAATACTAAACACACACCACAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:41830512..41830707 26863196 MeRIP-seq:(Medium) rs1264192183 Functional Loss SNV dbSNP153 33..33 33 - - - 61946 RMVar_ID_61946 Human_SNP_ID_695720172 m1A Human chr21 + 41844681 41844680 41844682 CACACATACACAGTCCCTCCCCCCTCACAGGGACACACACAGCCCCTCCTCCATCACAGGGACAC CACACATACACAGTCCCTCCCCCCTCACAGGG__ACACACAGCCCCTCCTCCATCACAGGGACAC GAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:41844677..41844771 26863196 MeRIP-seq:(Medium) rs1266790081 Functional Loss DEL dbSNP153 33..34 33 - - - 61947 RMVar_ID_61947 Human_SNP_ID_695722770 m1A Human chr21 - 41854664 41854664 41854664 CGGCAGCGACGTGTACTTCACCACCTCCAGAGACATCCCCCCGGGTACCGAGCTGCGCGTGTGGT CGGCAGCGACGTGTACTTCACCACCTCCAGAGGCATCCCCCCGGGTACCGAGCTGCGCGTGTGGT T C PRDM15 Ensembl:ENSG00000141956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41854613..41854757 26863196 MeRIP-seq:(Medium) rs1390931092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150740,Human_RBP_ID_572747,Human_RBP_ID_927735 Human_Splice_Rec_2124599,Human_Splice_Rec_2124649,Human_Splice_Rec_2124697,Human_Splice_Rec_2124743,Human_Splice_Rec_2124791,Human_Splice_Rec_2124851,Human_Splice_Rec_2124899,Human_Splice_Rec_2124963 RMVar_hsa_circ_34145,RMVar_hsa_circ_59160,RMVar_hsa_circ_212397,RMVar_hsa_circ_124600,RMVar_hsa_circ_326487,RMVar_hsa_circ_270216,RMVar_hsa_circ_373082,RMVar_hsa_circ_212398,RMVar_hsa_circ_212399 61948 RMVar_ID_61948 Human_SNP_ID_695729422 m1A Human chr21 + 41877087 41877087 41877087 GCTCATCCCACCCCAGGGCCTTTGCATTTGCCACCATCTGCCTGGTGGGGGCAGGCACCACCGCA GCTCATCCCACCCCAGGGCCTTTGCATTTGCCGCCATCTGCCTGGTGGGGGCAGGCACCACCGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:41877073..41877315 26863196 MeRIP-seq:(Medium) rs1569035924 Functional Loss SNV dbSNP153 33..33 33 - - - 61949 RMVar_ID_61949 Human_SNP_ID_695730269 m1A Human chr21 - 41879421 41879395 41879421 GCAGTCCCACCCGCAGGACCCCCGGCCGCGCCAGGGTCTCGCCTGCGCCCCCCGCGCCCGCCCGC GCAGTCCCACCCGCAGGACCCCCGGCCGCGCC__________________________CGCCCGC GGGCGCGGGGGGCGCAGGCGAGACCCT G PRDM15 Ensembl:ENSG00000141956 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:41879373..41879580 26863196 MeRIP-seq:(Medium) rs1474594562 Functional Loss DEL dbSNP153 33..58 33 - - - 61950 RMVar_ID_61950 Human_SNP_ID_695746760 m1A Human chr21 - 41942196 41942196 41942196 CTTTGAGGAGGACCCGCGGCAGCAGGCACTGGAGCTGGTGGTGCAGGAGGTCTCCAGCGTGCTCA CTTTGAGGAGGACCCGCGGCAGCAGGCACTGGGGCTGGTGGTGCAGGAGGTCTCCAGCGTGCTCA T C C2CD2 Ensembl:ENSG00000157617 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:41942145..41942281 26863196 MeRIP-seq:(Medium) rs1428671081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928178,Human_RBP_ID_4679748,Human_RBP_ID_19006712 Human_Splice_Rec_2125076,Human_Splice_Rec_2125077,Human_Splice_Rec_2125151 RMVar_hsa_circ_39121,RMVar_hsa_circ_212406 61951 RMVar_ID_61951 Human_SNP_ID_695749910 m1A Human chr21 + 41953783 41953771 41953783 TGGAGGGGGCGCGGCGGGGTCGGAGCCCGGCGAGGAGCGTGGCCGGGGGCCTCTGGGCGGGCAAG TGGAGGGGGCGCGGCGGGGTC____________GGAGCGTGGCCGGGGGCCTCTGGGCGGGCAAG CGGAGCCCGGCGA C HSALNG0133268 RNACentral:URS0000E95DBA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:41953735..41953968 26863196 MeRIP-seq:(Medium) rs1259424036 Functional Loss DEL dbSNP153 22..33 33 - - - 61952 RMVar_ID_61952 Human_SNP_ID_695749918 m1A Human chr21 + 41953783 41953783 41953783 TGGAGGGGGCGCGGCGGGGTCGGAGCCCGGCGAGGAGCGTGGCCGGGGGCCTCTGGGCGGGCAAG TGGAGGGGGCGCGGCGGGGTCGGAGCCCGGCGGGGAGCGTGGCCGGGGGCCTCTGGGCGGGCAAG A G HSALNG0133268 RNACentral:URS0000E95DBA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:41953735..41953968 26863196 MeRIP-seq:(Medium) rs979494196 Functional Loss SNV dbSNP153 33..33 33 - - - 61953 RMVar_ID_61953 Human_SNP_ID_695749925 m1A Human chr21 - 41953804 41953804 41953804 CCGCCGCGCGTTTCCTCCCCGCTTGCCCGCCCAGAGGCCCCCGGCCACGCTCCTCGCCGGGCTCC CCGCCGCGCGTTTCCTCCCCGCTTGCCCGCCCCGAGGCCCCCGGCCACGCTCCTCGCCGGGCTCC T G C2CD2 Ensembl:ENSG00000157617 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41953761..41953960 26863196 MeRIP-seq:(Medium) rs1402920128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679751,Human_RBP_ID_9332138 61954 RMVar_ID_61954 Human_SNP_ID_695750291 m1A Human chr21 - 41954764 41954764 41954764 ACACACCCATGCACCACACCGACACACCACACACGCACCACACCACATGCACCACGCTTACACAT ACACACCCATGCACCACACCGACACACCACACTCGCACCACACCACATGCACCACGCTTACACAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:41954542..41955214 26863196 MeRIP-seq:(Medium) rs949226535 Functional Loss SNV dbSNP153 33..33 33 - - - 61955 RMVar_ID_61955 Human_SNP_ID_695750325 m1A Human chr21 + 41954865 41954861 41954865 TGTGTGTGGTGTGTGGTGCACAGGATGGTGCGAGTGTGTATGGTGGTGCATGGGTGTGTATGTGT TGTGTGTGGTGTGTGGTGCACAGGATGGT____GTGTGTATGGTGGTGCATGGGTGTGTATGTGT TGCGA T HSALNG0133268 RNACentral:URS0000E95DBA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:41954548..41955141;chr21:41954559..41954959 26863196 MeRIP-seq:(Medium) rs1484014561 Functional Loss DEL dbSNP153 30..33 33 - - - 61956 RMVar_ID_61956 Human_SNP_ID_695750423 m1A Human chr21 - 41955088 41955086 41955089 CACACTGACACACCACATACATACACCACACCACATCACACATACACACCACACACACCACATGC CACACTGACACACCACATACATACACCACAC___ATCACACATACACACCACACACACCACATGC TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:41955041..41955156 26863196 MeRIP-seq:(Medium) rs775063576 Functional Loss DEL dbSNP153 32..34 33 - - - 61957 RMVar_ID_61957 Human_SNP_ID_695762794 m1A Human chr21 + 42002916 42002916 42002916 CCGGCTTGCTTACCACTTTGATCCTCGCACACAAATAGCTTCCCAAAGCCTTCCTGGATTGTTTC CCGGCTTGCTTACCACTTTGATCCTCGCACACTAATAGCTTCCCAAAGCCTTCCTGGATTGTTTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:42002912..42003007 26863196 MeRIP-seq:(Medium) rs1357357886 Functional Loss SNV dbSNP153 33..33 33 - - - 61958 RMVar_ID_61958 Human_SNP_ID_695764622 m1A Human chr21 + 42009480 42009480 42009480 TGCCCCTCCAGCCGCGGACCTCGGACGGGGGGAAGGGGGCTCCTCCAAGCGGGGAGACGGTCGCC TGCCCCTCCAGCCGCGGACCTCGGACGGGGGGGAGGGGGCTCCTCCAAGCGGGGAGACGGTCGCC A G ZNF295-AS1 Ensembl:ENSG00000237232 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:42009436..42022070 32194978 MeRIP-seq:(Medium) rs1459909766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8207042 61959 RMVar_ID_61959 Human_SNP_ID_695764989 m1A Human chr21 + 42010316 42010316 42010316 CTTTCCGCTCACACTCGGCTCGCGCGCGCCGCAGCCGCCGCTGCCGCTGTGATTCCATCCATCTT CTTTCCGCTCACACTCGGCTCGCGCGCGCCGCCGCCGCCGCTGCCGCTGTGATTCCATCCATCTT A C ZNF295-AS1 Ensembl:ENSG00000237232 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:42010231..42010333;chr21:42010234..42010334;chr21:42009534..42022070 26863196 MeRIP-seq:(Medium) rs1273653964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928475 61960 RMVar_ID_61960 Human_SNP_ID_695864098 m1A Human chr21 + 42371513 42371513 42371513 CACCACTCACTTCCTCCGGACACCACTCACACACTGTGGCCACCACTCAGACCCTCCATCCAGGT CACCACTCACTTCCTCCGGACACCACTCACACGCTGTGGCCACCACTCAGACCCTCCATCCAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42370838..42371710 26863196 MeRIP-seq:(Medium) rs1234940264 Functional Loss SNV dbSNP153 33..33 33 - - - 61961 RMVar_ID_61961 Human_SNP_ID_695865402 m1A Human chr21 + 42375319 42375319 42375319 ATCCCTGGCTCCCAGCGAGGTTCCAGCCCCTCAGCAGGCAGGCAAGGTCCTCTCCCGCACTGTCT ATCCCTGGCTCCCAGCGAGGTTCCAGCCCCTCCGCAGGCAGGCAAGGTCCTCTCCCGCACTGTCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:42375313..42375563 26863196 MeRIP-seq:(Medium) rs1032385746 Functional Loss SNV dbSNP153 33..33 33 - - - 61962 RMVar_ID_61962 Human_SNP_ID_695871547 m1A Human chr21 - 42396005 42396005 42396005 GAGCCAGGAAAGGGCTGTGTTTATGGGAAGCCAGTAACACTGTGGCCTACTATCTCTTCCGTGGT GAGCCAGGAAAGGGCTGTGTTTATGGGAAGCCGGTAACACTGTGGCCTACTATCTCTTCCGTGGT T C TMPRSS3 Ensembl:ENSG00000160183 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:42395901..42396028 26863196 MeRIP-seq:(Medium) rs752961392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2125773,Human_Splice_Rec_2125797,Human_Splice_Rec_2125889,Human_Splice_Rec_2125913 61963 RMVar_ID_61963 Human_SNP_ID_695898432 m1A Human chr21 + 42496176 42496176 42496176 TCTCTCCCTCCTCCTCCAACTCCTCCGAGCCCAGGTCCGACATGGTCTCGCCCCAGCCTGGATCA TCTCTCCCTCCTCCTCCAACTCCTCCGAGCCCCGGTCCGACATGGTCTCGCCCCAGCCTGGATCA A C SLC37A1 Ensembl:ENSG00000160190 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:42496101..42496229 26863196 MeRIP-seq:(Medium) rs144240955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2126129,Human_Splice_Rec_2126131 Clinvar_Rec_224 61964 RMVar_ID_61964 Human_SNP_ID_695898433 m1A Human chr21 + 42496176 42496176 42496176 TCTCTCCCTCCTCCTCCAACTCCTCCGAGCCCAGGTCCGACATGGTCTCGCCCCAGCCTGGATCA TCTCTCCCTCCTCCTCCAACTCCTCCGAGCCCGGGTCCGACATGGTCTCGCCCCAGCCTGGATCA A G SLC37A1 Ensembl:ENSG00000160190 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:42496101..42496229 26863196 MeRIP-seq:(Medium) rs144240955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2126129,Human_Splice_Rec_2126131 Clinvar_Rec_224 61965 RMVar_ID_61965 Human_SNP_ID_695943888 m1A Human chr21 - 42668891 42668891 42668891 GGCCCGCGTGGGACGTGGCGGGGGGTGGAGGGAGCAGCTCTGATAATCCGTGGGGAATTCCTCTC GGCCCGCGTGGGACGTGGCGGGGGGTGGAGGGGGCAGCTCTGATAATCCGTGGGGAATTCCTCTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:42668885..42669035 26863196 MeRIP-seq:(Medium) rs1379440634 Functional Loss SNV dbSNP153 33..33 33 - - - 61966 RMVar_ID_61966 Human_SNP_ID_695953315 m1A Human chr21 + 42703439 42703439 42703439 AGGACACCATCGGGAGCAGAGGGGAAGCCATAAAGCCCTGGAGGCAGGAAGAGGCAAAGGCTGGC AGGACACCATCGGGAGCAGAGGGGAAGCCATACAGCCCTGGAGGCAGGAAGAGGCAAAGGCTGGC A C PDE9A Ensembl:ENSG00000160191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42703426..42703567 26863196 MeRIP-seq:(Medium) rs1174223963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10096,RMVar_hsa_circ_123048,RMVar_hsa_circ_337612,RMVar_hsa_circ_79156,RMVar_hsa_circ_48585,RMVar_hsa_circ_64806,RMVar_hsa_circ_212424,RMVar_hsa_circ_212423 61967 RMVar_ID_61967 Human_SNP_ID_695960302 m1A Human chr21 + 42731851 42731851 42731851 ACCACTGAGGGACAGACGGGTTGTGGGCCTGGAGCAGCCCCGGAGGGAAGGAGCATTTGAAAGTG ACCACTGAGGGACAGACGGGTTGTGGGCCTGGGGCAGCCCCGGAGGGAAGGAGCATTTGAAAGTG A G PDE9A Ensembl:ENSG00000160191 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42731831..42731905 26863196 MeRIP-seq:(Medium) rs1363253948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19007109 Human_Splice_Rec_2126258,Human_Splice_Rec_2126259,Human_Splice_Rec_2126384,Human_Splice_Rec_2126385,Human_Splice_Rec_2126490,Human_Splice_Rec_2126491,Human_Splice_Rec_2126660,Human_Splice_Rec_2126661,Human_Splice_Rec_2126728,Human_Splice_Rec_2126729,Human_Splice_Rec_2126764,Human_Splice_Rec_2126765,Human_Splice_Rec_2126989 RMVar_hsa_circ_10096,RMVar_hsa_circ_123048,RMVar_hsa_circ_337612,RMVar_hsa_circ_79156,RMVar_hsa_circ_48585,RMVar_hsa_circ_64806,RMVar_hsa_circ_212424,RMVar_hsa_circ_212423,RMVar_hsa_circ_212426 61968 RMVar_ID_61968 Human_SNP_ID_695989563 m1A Human chr21 - 42837374 42837374 42837374 ATGTGGCAGTGGCAGAGTGTGGGGTGAGAGCCACGAAGAGAGGAGGTCACTGAGGTGGACAGTGG ATGTGGCAGTGGCAGAGTGTGGGGTGAGAGCCGCGAAGAGAGGAGGTCACTGAGGTGGACAGTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42837324..42837445 26863196 MeRIP-seq:(Medium) rs945063693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14317058,Human_RBP_ID_23928488 61969 RMVar_ID_61969 Human_SNP_ID_695989644 m1A Human chr21 + 42837628 42837628 42837628 CCACCCCAAGTCCCCACCTGGGCTTCTGCTGCACCCCCGCTGCCCTCCCTCCCGCTGGCCGGCAG CCACCCCAAGTCCCCACCTGGGCTTCTGCTGCTCCCCCGCTGCCCTCCCTCCCGCTGGCCGGCAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:42837578..42838019 26863196 MeRIP-seq:(Medium) rs531623350 Functional Loss SNV dbSNP153 33..33 33 - - - 61970 RMVar_ID_61970 Human_SNP_ID_695989722 m1A Human chr21 - 42837808 42837808 42837808 CAGAGGACAAGGACGGGGCCAGGGCAGGGGCCAGGGTTGGCAGAGGGCGGAGGGTGGGGAGGGCG CAGAGGACAAGGACGGGGCCAGGGCAGGGGCCGGGGTTGGCAGAGGGCGGAGGGTGGGGAGGGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:42837785..42837926 26863196 MeRIP-seq:(Medium) rs2156317 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7585,GWAS_ID_7586,GWAS_ID_7587,GWAS_ID_7588,GWAS_ID_7589,GWAS_ID_7590,GWAS_ID_7591,GWAS_ID_7592,GWAS_ID_7593,GWAS_ID_7594,GWAS_ID_7595,GWAS_ID_7596,GWAS_ID_7597,GWAS_ID_7598 61971 RMVar_ID_61971 Human_SNP_ID_695993750 m1A Human chr21 + 42848975 42848975 42848975 CACGATCACGCGGCGCGCACCTCACTCACAGCACACGATCACGCAGCGTGCACCTCACACACAGC CACGATCACGCGGCGCGCACCTCACTCACAGCGCACGATCACGCAGCGTGCACCTCACACACAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:42843193..42849287 32194978 MeRIP-seq:(Medium) rs1459162725 Functional Loss SNV dbSNP153 33..33 33 - - - 61972 RMVar_ID_61972 Human_SNP_ID_695993895 m1A Human chr21 + 42849168 42849164 42849168 CACAGCACACGATCACGCAGCGTGCACCTCACACACACACAGCGCACAATCACACCGCGCACCTC CACAGCACACGATCACGCAGCGTGCACCT____CACACACAGCGCACAATCACACCGCGCACCTC TCACA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42849119..42849252 26863196 MeRIP-seq:(Medium) rs560942483 Functional Loss DEL dbSNP153 30..33 33 - - - 61973 RMVar_ID_61973 Human_SNP_ID_695993896 m1A Human chr21 + 42849168 42849164 42849168 CACAGCACACGATCACGCAGCGTGCACCTCACACACACACAGCGCACAATCACACCGCGCACCTC CACAGCACACGATCACGCAGCGTGCACCTCA__CACACACAGCGCACAATCACACCGCGCACCTC TCACA TCA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42849119..42849252 26863196 MeRIP-seq:(Medium) rs560942483 Functional Loss DEL dbSNP153 32..33 33 - - - 61974 RMVar_ID_61974 Human_SNP_ID_695996215 m1A Human chr21 - 42855774 42855774 42855774 CTAACCTGTGTGTTTGGTTTGTGCAGGACGGCACCCTGAGGCTCTGGGAGTACAGGAGCGGCCGC CTAACCTGTGTGTTTGGTTTGTGCAGGACGGCTCCCTGAGGCTCTGGGAGTACAGGAGCGGCCGC T A WDR4 Ensembl:ENSG00000160193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:42850032..42862340 32194978 MeRIP-seq:(Medium) rs1296615324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961257,Human_RBP_ID_5386821,Human_RBP_ID_14318144,Human_RBP_ID_19006724,Human_RBP_ID_22673082,Human_RBP_ID_23009751 Human_Splice_Rec_2127062,Human_Splice_Rec_2127063,Human_Splice_Rec_2127084,Human_Splice_Rec_2127085,Human_Splice_Rec_2127104,Human_Splice_Rec_2127105,Human_Splice_Rec_2127124,Human_Splice_Rec_2127125,Human_Splice_Rec_2127144,Human_Splice_Rec_2127145,Human_Splice_Rec_2127158 RMVar_hsa_circ_2661,RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_99694,RMVar_hsa_circ_212432,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_120575,RMVar_hsa_circ_101683,RMVar_hsa_circ_289252,RMVar_hsa_circ_212435,RMVar_hsa_circ_212436,RMVar_hsa_circ_356789,RMVar_hsa_circ_212434,RMVar_hsa_circ_297383,RMVar_hsa_circ_289180,RMVar_hsa_circ_315645,RMVar_hsa_circ_212438,RMVar_hsa_circ_290281,RMVar_hsa_circ_20003,RMVar_hsa_circ_19239,RMVar_hsa_circ_212439,RMVar_hsa_circ_122175,RMVar_hsa_circ_212440,RMVar_hsa_circ_355744 61975 RMVar_ID_61975 Human_SNP_ID_695997529 m1A Human chr21 + 42859957 42859957 42859957 GGGAGGTGAGTGAGGTCATTCCTGGGTCCCCAACAGCACAGCAACCTCTAACCCAGGCCGCTCCT GGGAGGTGAGTGAGGTCATTCCTGGGTCCCCAGCAGCACAGCAACCTCTAACCCAGGCCGCTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:42859955..42860090;chr21:42859952..42860081 26863196 MeRIP-seq:(Medium) rs1397552650 Functional Loss SNV dbSNP153 33..33 33 - - - 61976 RMVar_ID_61976 Human_SNP_ID_695998296 m1A Human chr21 + 42862373 42862373 42862373 GATCTTCTCGTCCCGGTCGGCAGTGAGGATGAAGCGGTCATCAGGACTCACAGCCTGCATCACCA GATCTTCTCGTCCCGGTCGGCAGTGAGGATGATGCGGTCATCAGGACTCACAGCCTGCATCACCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42862326..42863639 26863196 MeRIP-seq:(Medium) rs1360096220 Functional Loss SNV dbSNP153 33..33 33 - - - 61977 RMVar_ID_61977 Human_SNP_ID_695998708 m1A Human chr21 - 42863531 42863529 42863532 CATAGCCTCGGAGGAGAAGGTCTTGGTGGCCGACAAGTCTGGAGACGTCTACTCCTTTTCGGTGC CATAGCCTCGGAGGAGAAGGTCTTGGTGGCC___AAGTCTGGAGACGTCTACTCCTTTTCGGTGC TGTC T WDR4 Ensembl:ENSG00000160193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:42863483..42876747 32194978 MeRIP-seq:(Medium) rs1278626433 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1937740,Human_RBP_ID_4673854,Human_RBP_ID_14318510,Human_RBP_ID_27028060,Human_RBP_ID_27301942 Human_Splice_Rec_2127056,Human_Splice_Rec_2127057,Human_Splice_Rec_2127078,Human_Splice_Rec_2127079,Human_Splice_Rec_2127098,Human_Splice_Rec_2127099,Human_Splice_Rec_2127118,Human_Splice_Rec_2127119,Human_Splice_Rec_2127138,Human_Splice_Rec_2127139,Human_Splice_Rec_2127152,Human_Splice_Rec_2127153,Human_Splice_Rec_2127164,Human_Splice_Rec_2127165 Human_miRNA_ID_2745956,Human_miRNA_ID_2745957,Human_miRNA_ID_2745958,Human_miRNA_ID_2745959 RMVar_hsa_circ_2661,RMVar_hsa_circ_102409,RMVar_hsa_circ_212433,RMVar_hsa_circ_120575,RMVar_hsa_circ_289252,RMVar_hsa_circ_212434,RMVar_hsa_circ_289180,RMVar_hsa_circ_315645,RMVar_hsa_circ_212438,RMVar_hsa_circ_212441,RMVar_hsa_circ_290281,RMVar_hsa_circ_20003,RMVar_hsa_circ_212439,RMVar_hsa_circ_355744,RMVar_hsa_circ_283309,RMVar_hsa_circ_293430,RMVar_hsa_circ_212442,RMVar_hsa_circ_212444,RMVar_hsa_circ_296263,RMVar_hsa_circ_302905,RMVar_hsa_circ_212443,RMVar_hsa_circ_330889 61978 RMVar_ID_61978 Human_SNP_ID_696002701 m1A Human chr21 + 42876605 42876605 42876605 TACTTATCTGCACCACTGTGTGACAGAAGCTAAGAATTCAGCAAGTAGGACAACAATTGCTTCTT TACTTATCTGCACCACTGTGTGACAGAAGCTACGAATTCAGCAAGTAGGACAACAATTGCTTCTT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:42876600..42876775 26863196 MeRIP-seq:(Medium) rs1016343920 Functional Loss SNV dbSNP153 33..33 33 - - - 61979 RMVar_ID_61979 Human_SNP_ID_696003604 m1A Human chr21 + 42879185 42879185 42879185 AGACCAGCCATCTAGTGCAAGGAGCGCGCCGGAGCCGGGGAGCGGACGCCGAGAGCGGACGGCGA AGACCAGCCATCTAGTGCAAGGAGCGCGCCGGCGCCGGGGAGCGGACGCCGAGAGCGGACGGCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42879178..42879287 26863196 MeRIP-seq:(Medium) rs986693333 Functional Loss SNV dbSNP153 33..33 33 - - - 61980 RMVar_ID_61980 Human_SNP_ID_696003736 m1A Human chr21 + 42879455 42879453 42879456 TGGCCAGGAATCGGCTGCCGCCCCGCACCACCAACGTCTGCCCGCACAACGCCAGTCCCACAGAG TGGCCAGGAATCGGCTGCCGCCCCGCACCAC___CGTCTGCCCGCACAACGCCAGTCCCACAGAG CCAA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:42879451..42879550 26863196 MeRIP-seq:(Medium) rs769417902 Functional Loss DEL dbSNP153 32..34 33 - - - 61981 RMVar_ID_61981 Human_SNP_ID_696003757 m1A Human chr21 + 42879484 42879484 42879484 ACCAACGTCTGCCCGCACAACGCCAGTCCCACAGAGCCCGCCATGTACCCGCCCGCCTCACCGCC ACCAACGTCTGCCCGCACAACGCCAGTCCCACCGAGCCCGCCATGTACCCGCCCGCCTCACCGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr21:42879164..42879550;chr21:42879194..42879550;chr21:42879385..42879525 26863196 MeRIP-seq:(Medium) rs779630985 Functional Loss SNV dbSNP153 33..33 33 - - - 61982 RMVar_ID_61982 Human_SNP_ID_696003758 m1A Human chr21 + 42879484 42879484 42879484 ACCAACGTCTGCCCGCACAACGCCAGTCCCACAGAGCCCGCCATGTACCCGCCCGCCTCACCGCC ACCAACGTCTGCCCGCACAACGCCAGTCCCACGGAGCCCGCCATGTACCCGCCCGCCTCACCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr21:42879164..42879550;chr21:42879194..42879550;chr21:42879385..42879525 26863196 MeRIP-seq:(Medium) rs779630985 Functional Loss SNV dbSNP153 33..33 33 - - - 61983 RMVar_ID_61983 Human_SNP_ID_696003772 m1A Human chr21 + 42879498 42879498 42879498 GCACAACGCCAGTCCCACAGAGCCCGCCATGTACCCGCCCGCCTCACCGCCATACACATGTGCCA GCACAACGCCAGTCCCACAGAGCCCGCCATGTCCCCGCCCGCCTCACCGCCATACACATGTGCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr21:42879378..42879550;chr21:42879149..42879568 26863196 MeRIP-seq:(Medium) rs771132429 Functional Loss SNV dbSNP153 33..33 33 - - - 61984 RMVar_ID_61984 Human_SNP_ID_696007439 m1A Human chr21 + 42893360 42893360 42893360 ACCGCCATGGCTGCCCCGTGTTTGCTGCGGCAAGGACGAGCCGGGGCGCTGAAGGTAAAGGAGGA ACCGCCATGGCTGCCCCGTGTTTGCTGCGGCATGGACGAGCCGGGGCGCTGAAGGTAAAGGAGGA A T NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42893301..42893432 26863196 MeRIP-seq:(Medium) rs1055927464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245151,Human_RBP_ID_572890,Human_RBP_ID_4679954,Human_RBP_ID_18423360,Human_RBP_ID_19110337,Human_RBP_ID_22083204,Human_RBP_ID_23009713,Human_RBP_ID_26821805 Human_Splice_Rec_2127177,Human_Splice_Rec_2127181,Human_Splice_Rec_2127187 RMVar_hsa_circ_109398,RMVar_hsa_circ_212448 61985 RMVar_ID_61985 Human_SNP_ID_696012847 m1A Human chr21 + 42910511 42910511 42910511 AAGAGGTGAAGTTTCTTGCAGTACAGGGACGAAGTAGGAAGAGGTGAAGTTTCGTGCAGTACAGG AAGAGGTGAAGTTTCTTGCAGTACAGGGACGATGTAGGAAGAGGTGAAGTTTCGTGCAGTACAGG A T NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42910465..42910613 26863196 MeRIP-seq:(Medium) rs1189965957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7049598,Human_RBP_ID_14320163,Human_RBP_ID_17146036,Human_RBP_ID_18326741 61986 RMVar_ID_61986 Human_SNP_ID_696012862 m1A Human chr21 + 42910549 42910549 42910549 AAGAGGTGAAGTTTCGTGCAGTACAGGGACGGAGTAGGAAGAGGTGAAGTTTCGTGCAGTACAGG AAGAGGTGAAGTTTCGTGCAGTACAGGGACGGCGTAGGAAGAGGTGAAGTTTCGTGCAGTACAGG A C NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:42910451..42910625;chr21:42910451..42910611;chr21:42910420..42910616 26863196 MeRIP-seq:(Medium) rs1013134009 Functional Loss SNV dbSNP153 33..33 33 - - - 61987 RMVar_ID_61987 Human_SNP_ID_696012894 m1A Human chr21 + 42910617 42910617 42910617 GGAGTAGGAAGAGGTGAAGTTTCGTGCGGTGCAGGGACGGAGTAGGAAGAGGTGAAGTTTCGTGC GGAGTAGGAAGAGGTGAAGTTTCGTGCGGTGCTGGGACGGAGTAGGAAGAGGTGAAGTTTCGTGC A T NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:42910480..42910639 26863196 MeRIP-seq:(Medium) rs1332493112 Functional Loss SNV dbSNP153 33..33 33 - - - 61988 RMVar_ID_61988 Human_SNP_ID_696012942 m1A Human chr21 - 42910745 42910745 42910745 AATAGCTCATTGAGTGCCTGTGGCCAGCGGGGAGCAACTTCGTCCCTGCACCGCACAAAACTTCA AATAGCTCATTGAGTGCCTGTGGCCAGCGGGGGGCAACTTCGTCCCTGCACCGCACAAAACTTCA T C ERVH48-1 RNACentral:URS0000D5A870 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:42910676..42910825;chr21:42910681..42910825;chr21:42910671..42910765 26863196 MeRIP-seq:(Medium) rs1202431709 Functional Loss SNV dbSNP153 33..33 33 - - - 61989 RMVar_ID_61989 Human_SNP_ID_696015831 m1A Human chr21 + 42921197 42921193 42921197 GACTCCATGCCGTTCGTCAGGATAGAGGGAGAAAGGTTTGGTGAGGTCTGGGAGGGTGAGGATGG GACTCCATGCCGTTCGTCAGGATAGAGGG____AGGTTTGGTGAGGTCTGGGAGGGTGAGGATGG GAGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42921162..42921299 26863196 MeRIP-seq:(Medium) rs1412803394 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23928832 61990 RMVar_ID_61990 Human_SNP_ID_696016071 m1A Human chr21 + 42922175 42922175 42922175 GATACTGCTTCTGTGATAGGAACTGGGTGGGGATTTTAAGGGTAATGCAGAAGGGGGTGTGGTGT GATACTGCTTCTGTGATAGGAACTGGGTGGGGGTTTTAAGGGTAATGCAGAAGGGGGTGTGGTGT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:42922094..42922223 26863196 MeRIP-seq:(Medium) rs1361508151 Functional Loss SNV dbSNP153 33..33 33 - - - 61991 RMVar_ID_61991 Human_SNP_ID_696016656 m1A Human chr21 + 42924205 42924205 42924205 AGGTGGCGGGGTGGGTTTACAGGCCTCAGGAGAGAGCGGTGGGGGAGGAGAATGGGTACAGGCAG AGGTGGCGGGGTGGGTTTACAGGCCTCAGGAGGGAGCGGTGGGGGAGGAGAATGGGTACAGGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42924155..42924453 26863196 MeRIP-seq:(Medium) rs1202268195 Functional Loss SNV dbSNP153 33..33 33 - - - 61992 RMVar_ID_61992 Human_SNP_ID_696023248 m1A Human chr21 - 42948749 42948746 42948749 AGAGACAGAGAGGAACAGACAAAGAGGGAGTCAAGGAGAGAGAGAGAAAGAGAGAGGCAGAGAGA AGAGACAGAGAGGAACAGACAAAGAGGGAGTC___GAGAGAGAGAGAAAGAGAGAGGCAGAGAGA CCTT C ERVH48-1,ERVH48-1:2 RNACentral:URS0000D5A870,RNACentral:URS0000D59CEE lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42948699..42948832 26863196 MeRIP-seq:(Medium) rs1234799716 Functional Loss DEL dbSNP153 33..35 33 - - - 61993 RMVar_ID_61993 Human_SNP_ID_696023262 m1A Human chr21 - 42948813 42948813 42948813 GAAAGAGCAGCAGAGAGAGAGAGAGGAAAGAGACAGAGAGGAAGAGAGGAAAAGAGAGAGAGGAA GAAAGAGCAGCAGAGAGAGAGAGAGGAAAGAGTCAGAGAGGAAGAGAGGAAAAGAGAGAGAGGAA T A ERVH48-1,ERVH48-1:2 RNACentral:URS0000D5A870,RNACentral:URS0000D59CEE lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42948680..42948878 26863196 MeRIP-seq:(Medium) rs189991815 Functional Loss SNV dbSNP153 33..33 33 - - - 61994 RMVar_ID_61994 Human_SNP_ID_696030973 m1A Human chr21 - 42974719 42974719 42974719 GCGGCGGCCGCGGGCCGGTGTGATTGATAGGGACGGCGGCGGCGAGAGCGGCGGCGGCGGCGGCG GCGGCGGCCGCGGGCCGGTGTGATTGATAGGGGCGGCGGCGGCGAGAGCGGCGGCGGCGGCGGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:42974698..42974875 26863196 MeRIP-seq:(Medium) rs1194232279 Functional Loss SNV dbSNP153 33..33 33 - - - 61995 RMVar_ID_61995 Human_SNP_ID_696031151 m1A Human chr21 - 42975098 42975057 42975098 CCGCCCCGGCCCCGCCCCGCCGCGCGCCCCCGACCCTCACGCCCGCCGCCCCGCCCGCGCCGGGC CCGCCCCGGCCCCGCCCCGCCGCGCGCCCCCG_________________________________ GCGCGCGGAGCCCGGCGCGGGCGGGGCGGCGGGCGTGAGGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:42974740..42975097 26863196 MeRIP-seq:(Medium) rs1184435428 Functional Loss DEL dbSNP153 33..65 33 - - - 61996 RMVar_ID_61996 Human_SNP_ID_696031173 m1A Human chr21 - 42975098 42975098 42975098 CCGCCCCGGCCCCGCCCCGCCGCGCGCCCCCGACCCTCACGCCCGCCGCCCCGCCCGCGCCGGGC CCGCCCCGGCCCCGCCCCGCCGCGCGCCCCCGCCCCTCACGCCCGCCGCCCCGCCCGCGCCGGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:42974740..42975097 26863196 MeRIP-seq:(Medium) rs1321864459 Functional Loss SNV dbSNP153 33..33 33 - - - 61997 RMVar_ID_61997 Human_SNP_ID_696031218 m1A Human chr21 + 42975198 42975186 42975198 GCGGAGTCCTCAGGGCCGGCGGGGCTGCTCGGAGGGTGCGGGGCGCGCGGCGGCGCAGGCGGGAA GCGGAGTCCTCAGGGCCGGCG____________GGGTGCGGGGCGCGCGGCGGCGCAGGCGGGAA GGGGCTGCTCGGA G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:42974688..42975437 26863196 MeRIP-seq:(Medium) rs1340827247 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_264854,Human_RBP_ID_780694,Human_RBP_ID_3665361,Human_RBP_ID_5240599,Human_RBP_ID_5323707,Human_RBP_ID_8115559,Human_RBP_ID_8205731,Human_RBP_ID_8235371,Human_RBP_ID_9431875,Human_RBP_ID_17144980,Human_RBP_ID_18423410,Human_RBP_ID_18496160,Human_RBP_ID_18952012,Human_RBP_ID_22723472,Human_RBP_ID_24425542,Human_RBP_ID_26788837 61998 RMVar_ID_61998 Human_SNP_ID_696031220 m1A Human chr21 - 42975194 42975194 42975194 CGCCTGCGCCGCCGCGCGCCCCGCACCCTCCGAGCAGCCCCGCCGGCCCTGAGGACTCCGCGAGG CGCCTGCGCCGCCGCGCGCCCCGCACCCTCCGGGCAGCCCCGCCGGCCCTGAGGACTCCGCGAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:42975117..42975577 26863196 MeRIP-seq:(Medium) rs954005029 Functional Loss SNV dbSNP153 33..33 33 - - - 61999 RMVar_ID_61999 Human_SNP_ID_696031372 m1A Human chr21 - 42975597 42975597 42975597 AACTGGTCCCGTCGCAGAGCCACTGTCCAAATAAGGCATTTCGAGAGCCACGAGGATGACATAAA AACTGGTCCCGTCGCAGAGCCACTGTCCAAATGAGGCATTTCGAGAGCCACGAGGATGACATAAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:42975160..42975735 26863196 MeRIP-seq:(Medium) rs1181756860 Functional Loss SNV dbSNP153 33..33 33 - - - 62000 RMVar_ID_62000 Human_SNP_ID_696036250 m1A Human chr21 - 42992764 42992743 42992764 GAGAACCCCCCAGTGCTGTGAGGAAGCCCCCAATGCTATGAGGGAACCCCCCAGTGCTGTGAGGG GAGAACCCCCCAGTGCTGTGAGGAAGCCCCCA_____________________GTGCTGTGAGGG CTGGGGGGTTCCCTCATAGCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42992484..42993090 26863196 MeRIP-seq:(Medium) rs1320933920 Functional Loss DEL dbSNP153 33..53 33 - - - 62001 RMVar_ID_62001 Human_SNP_ID_696036259 m1A Human chr21 - 42992764 42992764 42992764 GAGAACCCCCCAGTGCTGTGAGGAAGCCCCCAATGCTATGAGGGAACCCCCCAGTGCTGTGAGGG GAGAACCCCCCAGTGCTGTGAGGAAGCCCCCAGTGCTATGAGGGAACCCCCCAGTGCTGTGAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42992484..42993090 26863196 MeRIP-seq:(Medium) rs1431276281 Functional Loss SNV dbSNP153 33..33 33 - - - 62002 RMVar_ID_62002 Human_SNP_ID_696037779 m1A Human chr21 + 42997849 42997849 42997849 GGGGAGGACTCAGGGGTGGGAGAGAACCTGGCATGCTGGGGAAGCTAAATGTGGCGATTGGTTTG GGGGAGGACTCAGGGGTGGGAGAGAACCTGGCGTGCTGGGGAAGCTAAATGTGGCGATTGGTTTG A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:42997822..42997905 26863196 MeRIP-seq:(Medium) rs955307119 Functional Loss SNV dbSNP153 33..33 33 - - - 62003 RMVar_ID_62003 Human_SNP_ID_696055287 m1A Human chr21 - 43067740 43067740 43067740 TTCGGAGGGAGGCAGGAAGGGTGCCGCGGAGAACCCCGCGACAGGGCCAGATGGAGGGGGTGGAG TTCGGAGGGAGGCAGGAAGGGTGCCGCGGAGAGCCCCGCGACAGGGCCAGATGGAGGGGGTGGAG T C CBS Ensembl:ENSG00000160200 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43067733..43067813 26863196 MeRIP-seq:(Medium) rs1359881224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832577 RMVar_hsa_circ_119851,RMVar_hsa_circ_48771,RMVar_hsa_circ_212472,RMVar_hsa_circ_212464,RMVar_hsa_circ_81093,RMVar_hsa_circ_265399,RMVar_hsa_circ_378073 62004 RMVar_ID_62004 Human_SNP_ID_696061091 m1A Human chr21 - 43095575 43095575 43095575 CATACATGAGTTATATCTAATGACACTTTGTAATGTATAACGAGTCTTAAACCACTGTGGTCTCC CATACATGAGTTATATCTAATGACACTTTGTAGTGTATAACGAGTCTTAAACCACTGTGGTCTCC T C U2AF1 Ensembl:ENSG00000160201 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2839634 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7599,GWAS_ID_7600,GWAS_ID_7601,GWAS_ID_7602 RMVar_hsa_circ_9251,RMVar_hsa_circ_104652,RMVar_hsa_circ_212479,RMVar_hsa_circ_305046,RMVar_hsa_circ_372065,RMVar_hsa_circ_212477,RMVar_hsa_circ_344149,RMVar_hsa_circ_77183,RMVar_hsa_circ_212481,RMVar_hsa_circ_29675,RMVar_hsa_circ_212480,RMVar_hsa_circ_103143,RMVar_hsa_circ_212478,RMVar_hsa_circ_212482 62005 RMVar_ID_62005 Human_SNP_ID_696063454 m1A Human chr21 - 43107569 43107569 43107569 GGGGCGGGGAAGAGCGTCGTCGCGTCCGGGTGACGTCTCCCGAGGGCGTCGGCAGGGTCGGCGGC GGGGCGGGGAAGAGCGTCGTCGCGTCCGGGTGTCGTCTCCCGAGGGCGTCGGCAGGGTCGGCGGC T A U2AF1 Ensembl:ENSG00000160201 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:43107487..43107572 26863410 MeRIP-seq:(Medium) rs1224216686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104652,RMVar_hsa_circ_212477,RMVar_hsa_circ_77183,RMVar_hsa_circ_212481 62006 RMVar_ID_62006 Human_SNP_ID_696069071 m1A Human chr21 - 43141546 43141546 43141546 GACAGAGGGAGAGGCAGGGGCCAGACAGCGCCAACCACCTGAGACCCAGGCAAGAGACAGTATGG GACAGAGGGAGAGGCAGGGGCCAGACAGCGCCGACCACCTGAGACCCAGGCAAGAGACAGTATGG T C FRGCA,FRGCA:2,FRGCA:3,FRGCA:4,FRGCA:5 RNACentral:URS00009B0429,RNACentral:URS0000D5CD69,RNACentral:URS00008B6D88,RNACentral:URS0000D58F94,RNACentral:URS0000D5D609 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43141492..43141576 26863196 MeRIP-seq:(Medium) rs67365181 Functional Loss SNV dbSNP153 33..33 33 - - - 62007 RMVar_ID_62007 Human_SNP_ID_696084232 m1A Human chr21 + 43210888 43210888 43210888 GGTGGGCCTGGGCTAGTCTGCTTTCTGTGGCCATGGAACTGGAGGGCCCAGGCATTCACCCATCT GGTGGGCCTGGGCTAGTCTGCTTTCTGTGGCCGTGGAACTGGAGGGCCCAGGCATTCACCCATCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43210839..43210982 26863196 MeRIP-seq:(Medium) rs1214303668 Functional Loss SNV dbSNP153 33..33 33 - - - 62008 RMVar_ID_62008 Human_SNP_ID_696084452 m1A Human chr21 + 43211687 43211685 43211687 GGAAGAAAGAGAGGGAGGGAAGGAGAGAGGCAAGAGAGAGAGAGGAGGGGAAGAAGGGAGGAGTC GGAAGAAAGAGAGGGAGGGAAGGAGAGAGGC__GAGAGAGAGAGGAGGGGAAGAAGGGAGGAGTC CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43211620..43211783 26863196 MeRIP-seq:(Medium) rs1039838315 Functional Loss DEL dbSNP153 32..33 33 - - - 62009 RMVar_ID_62009 Human_SNP_ID_696084737 m1A Human chr21 + 43262709 43262709 43262709 AAAGTGGTGGTGGTGGTGGTGGGAGTGAAGGTAGTGGTGGTGGTGATGGTGGTGGTGGTGGTGGG AAAGTGGTGGTGGTGGTGGTGGGAGTGAAGGTGGTGGTGGTGGTGATGGTGGTGGTGGTGGTGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:43262606..43262733 26863196 MeRIP-seq:(Medium) rs1343724770 Functional Loss SNV dbSNP153 33..33 33 - - - 62010 RMVar_ID_62010 Human_SNP_ID_696084738 m1A Human chr21 - 43262720 43262720 43262720 CCACCTTCACTCCCACCACCACCACCACCATCACCACCACCACTACCTTCACTCCCACCACCACC CCACCTTCACTCCCACCACCACCACCACCATCGCCACCACCACTACCTTCACTCCCACCACCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43262660..43262852 26863196 MeRIP-seq:(Medium) rs1274698802 Functional Loss SNV dbSNP153 33..33 33 - - - 62011 RMVar_ID_62011 Human_SNP_ID_696084739 m1A Human chr21 - 43262720 43262720 43262720 CCACCTTCACTCCCACCACCACCACCACCATCACCACCACCACTACCTTCACTCCCACCACCACC CCACCTTCACTCCCACCACCACCACCACCATCCCCACCACCACTACCTTCACTCCCACCACCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43262660..43262852 26863196 MeRIP-seq:(Medium) rs1274698802 Functional Loss SNV dbSNP153 33..33 33 - - - 62012 RMVar_ID_62012 Human_SNP_ID_696105674 m1A Human chr21 + 43336504 43336501 43336504 CACCATCACCACCATCACCATCACCACCACCAACACCACCACCAACCCCACCACCACCACCATCA CACCATCACCACCATCACCATCACCACCAC___CACCACCACCAACCCCACCACCACCACCATCA CCAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43336467..43336615 26863196 MeRIP-seq:(Medium) rs1212497502 Functional Loss DEL dbSNP153 31..33 33 - - - 62013 RMVar_ID_62013 Human_SNP_ID_696105678 m1A Human chr21 + 43336504 43336504 43336504 CACCATCACCACCATCACCATCACCACCACCAACACCACCACCAACCCCACCACCACCACCATCA CACCATCACCACCATCACCATCACCACCACCACCACCACCACCAACCCCACCACCACCACCATCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43336467..43336615 26863196 MeRIP-seq:(Medium) rs932354517 Functional Loss SNV dbSNP153 33..33 33 - - - 62014 RMVar_ID_62014 Human_SNP_ID_696105679 m1A Human chr21 + 43336504 43336504 43336504 CACCATCACCACCATCACCATCACCACCACCAACACCACCACCAACCCCACCACCACCACCATCA CACCATCACCACCATCACCATCACCACCACCATCACCACCACCAACCCCACCACCACCACCATCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43336467..43336615 26863196 MeRIP-seq:(Medium) rs932354517 Functional Loss SNV dbSNP153 33..33 33 - - - 62015 RMVar_ID_62015 Human_SNP_ID_696106205 m1A Human chr21 + 43337151 43337110 43337152 CCACCATCAACATCACCACCATCACCATCAGCATCATCATCACCACCACCACCATCACCACCACC __________________________________CATCATCACCACCACCACCATCACCACCACC CCATCATCACCACCATCAACATCACCACCATCACCATCAGCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43337100..43337218 26863196 MeRIP-seq:(Medium) rs1388371575 Functional Loss DEL dbSNP153 1..34 33 - - - 62016 RMVar_ID_62016 Human_SNP_ID_696106229 m1A Human chr21 - 43337140 43337140 43337140 TGGTGGTGGTGGTGATGATGATGCTGATGGTGATGGTGGTGATGTTGATGGTGGTGATGATGGTG TGGTGGTGGTGGTGATGATGATGCTGATGGTGGTGGTGGTGATGTTGATGGTGGTGATGATGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43336929..43337385 26863196 MeRIP-seq:(Medium) rs1252905347 Functional Loss SNV dbSNP153 33..33 33 - - - 62017 RMVar_ID_62017 Human_SNP_ID_696106232 m1A Human chr21 + 43337151 43337149 43337152 CCACCATCAACATCACCACCATCACCATCAGCATCATCATCACCACCACCACCATCACCACCACC CCACCATCAACATCACCACCATCACCATCAG___CATCATCACCACCACCACCATCACCACCACC GCAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43337100..43337218 26863196 MeRIP-seq:(Medium) rs1260063201 Functional Loss DEL dbSNP153 32..34 33 - - - 62018 RMVar_ID_62018 Human_SNP_ID_696107438 m1A Human chr21 + 43340718 43340718 43340718 AGCTGAGGTGGGGTGTTTGAGCCGAGGAGCAGAGGGCGTCTGCAGAGGTGAGCTGAGGGAGGCAG AGCTGAGGTGGGGTGTTTGAGCCGAGGAGCAGCGGGCGTCTGCAGAGGTGAGCTGAGGGAGGCAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43340670..43340876 26863196 MeRIP-seq:(Medium) rs1258092747 Functional Loss SNV dbSNP153 33..33 33 - - - 62019 RMVar_ID_62019 Human_SNP_ID_696107439 m1A Human chr21 + 43340718 43340718 43340718 AGCTGAGGTGGGGTGTTTGAGCCGAGGAGCAGAGGGCGTCTGCAGAGGTGAGCTGAGGGAGGCAG AGCTGAGGTGGGGTGTTTGAGCCGAGGAGCAGGGGGCGTCTGCAGAGGTGAGCTGAGGGAGGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43340670..43340876 26863196 MeRIP-seq:(Medium) rs1258092747 Functional Loss SNV dbSNP153 33..33 33 - - - 62020 RMVar_ID_62020 Human_SNP_ID_696133702 m1A Human chr21 - 43451552 43451552 43451552 GCTGGAGGGGCCTGGGAGTCCCAGCGGGCGAGAAAGCCGGGCCCAGGGGAGAGCAGCATGCTGGG GCTGGAGGGGCCTGGGAGTCCCAGCGGGCGAGGAAGCCGGGCCCAGGGGAGAGCAGCATGCTGGG T C LINC00313 RNACentral:URS00008BFDE1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43451514..43451586 26863196 MeRIP-seq:(Medium) rs162387 Functional Loss SNV dbSNP153 33..33 33 - - - 62021 RMVar_ID_62021 Human_SNP_ID_696134833 m1A Human chr21 + 43458113 43458113 43458113 CCACCCTGCCAAGTGTGGTCCCTGGGCCCCCGACTTCCCTTCTCAGCCTCTGCCCCTGGGTCTGG CCACCCTGCCAAGTGTGGTCCCTGGGCCCCCGCCTTCCCTTCTCAGCCTCTGCCCCTGGGTCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:43458085..43458159;chr21:43458076..43458170 26863196 MeRIP-seq:(Medium) rs463194 Functional Loss SNV dbSNP153 33..33 33 - - - 62022 RMVar_ID_62022 Human_SNP_ID_696134834 m1A Human chr21 + 43458113 43458113 43458113 CCACCCTGCCAAGTGTGGTCCCTGGGCCCCCGACTTCCCTTCTCAGCCTCTGCCCCTGGGTCTGG CCACCCTGCCAAGTGTGGTCCCTGGGCCCCCGGCTTCCCTTCTCAGCCTCTGCCCCTGGGTCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:43458085..43458159;chr21:43458076..43458170 26863196 MeRIP-seq:(Medium) rs463194 Functional Loss SNV dbSNP153 33..33 33 - - - 62023 RMVar_ID_62023 Human_SNP_ID_696134835 m1A Human chr21 - 43458120 43458120 43458120 GCATGCCCCAGACCCAGGGGCAGAGGCTGAGAAGGGAAGTCGGGGGCCCAGGGACCACACTTGGC GCATGCCCCAGACCCAGGGGCAGAGGCTGAGAGGGGAAGTCGGGGGCCCAGGGACCACACTTGGC T C LINC00313,LINC00313:2,LINC00313:3,LINC00313:4,LINC00313:5 RNACentral:URS00008BF52B,RNACentral:URS00008BFDE1,RNACentral:URS00009C1496,RNACentral:URS0000D5A6FA,RNACentral:URS00009BD454 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:43458100..43458227 26863196 MeRIP-seq:(Medium) rs1308772602 Functional Loss SNV dbSNP153 33..33 33 - - - 62024 RMVar_ID_62024 Human_SNP_ID_696135057 m1A Human chr21 - 43459220 43459219 43459220 GGCGGGGTCATCCGTCATCACCTGGGTGCCGGAGGACGAGCATGCTGCCCTGACGAGGATGATCA GGCGGGGTCATCCGTCATCACCTGGGTGCCGG_GGACGAGCATGCTGCCCTGACGAGGATGATCA CT C LINC00313,LINC00313:2,LINC00313:3,LINC00313:4,LINC00313:5 RNACentral:URS00008BF52B,RNACentral:URS00008BFDE1,RNACentral:URS00009C1496,RNACentral:URS0000D5A6FA,RNACentral:URS00009BD454 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43459188..43459267 26863196 MeRIP-seq:(Medium) rs1313572971 Functional Loss DEL dbSNP153 33..33 33 - - - 62025 RMVar_ID_62025 Human_SNP_ID_696136802 m1A Human chr21 + 43467804 43467804 43467804 CACCACACCACAAACCACACACCACACATTACACAGCACACCACACACACACACCACACACACCA CACCACACCACAAACCACACACCACACATTACCCAGCACACCACACACACACACCACACACACCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:43467722..43467867 26863196 MeRIP-seq:(Medium) rs1368297817 Functional Loss SNV dbSNP153 33..33 33 - - - 62026 RMVar_ID_62026 Human_SNP_ID_696136960 m1A Human chr21 + 43467933 43467933 43467933 ACACGCACCACACACCACACACACCACACACCACACACACACACCACACACACCACACTTACACC ACACGCACCACACACCACACACACCACACACCCCACACACACACCACACACACCACACTTACACC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:43467930..43468015 26863410 MeRIP-seq:(Medium) rs1166994545 Functional Loss SNV dbSNP153 33..33 33 - - - 62027 RMVar_ID_62027 Human_SNP_ID_696137094 m1A Human chr21 + 43468046 43468024 43468047 ACCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACA ACCATACACAC_______________________CCATACCACACACACCATACCACAAACCACA CAGCACACACCACACCACACACAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43467651..43468177 26863196 MeRIP-seq:(Medium) rs1196812849 Functional Loss DEL dbSNP153 12..34 33 - - - 62028 RMVar_ID_62028 Human_SNP_ID_696137094 m1A Human chr21 + 43468047 43468024 43468047 CCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACAC CCATACACAC_______________________CCATACCACACACACCATACCACAAACCACAC CAGCACACACCACACCACACACAA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:43467919..43468127 26863196 MeRIP-seq:(Medium) rs1196812849 Functional Loss DEL dbSNP153 11..33 33 - - - 62029 RMVar_ID_62029 Human_SNP_ID_696137129 m1A Human chr21 + 43468047 43468042 43468048 CCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACAC CCATACACACAGCACACACCACACCACA______CATACCACACACACCATACCACAAACCACAC ACACAAC A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:43467919..43468127 26863196 MeRIP-seq:(Medium) rs1569027607 Functional Loss DEL dbSNP153 29..34 33 - - - 62030 RMVar_ID_62030 Human_SNP_ID_696137130 m1A Human chr21 + 43468046 43468043 43468046 ACCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACA ACCATACACACAGCACACACCACACCACAC___ACCATACCACACACACCATACCACAAACCACA CACA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43467651..43468177 26863196 MeRIP-seq:(Medium) rs1249407549 Functional Loss DEL dbSNP153 31..33 33 - - - 62031 RMVar_ID_62031 Human_SNP_ID_696137132 m1A Human chr21 + 43468046 43468045 43468047 ACCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACA ACCATACACACAGCACACACCACACCACACAC__CCATACCACACACACCATACCACAAACCACA CAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43467651..43468177 26863196 MeRIP-seq:(Medium) rs1420524458 Functional Loss DEL dbSNP153 33..34 33 - - - 62032 RMVar_ID_62032 Human_SNP_ID_696137132 m1A Human chr21 + 43468047 43468045 43468047 CCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACAC CCATACACACAGCACACACCACACCACACAC__CCATACCACACACACCATACCACAAACCACAC CAA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:43467919..43468127 26863196 MeRIP-seq:(Medium) rs1420524458 Functional Loss DEL dbSNP153 32..33 33 - - - 62033 RMVar_ID_62033 Human_SNP_ID_696137133 m1A Human chr21 + 43468046 43468046 43468046 ACCATACACACAGCACACACCACACCACACACAACCATACCACACACACCATACCACAAACCACA ACCATACACACAGCACACACCACACCACACACCACCATACCACACACACCATACCACAAACCACA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43467651..43468177 26863196 MeRIP-seq:(Medium) rs1229423639 Functional Loss SNV dbSNP153 33..33 33 - - - 62034 RMVar_ID_62034 Human_SNP_ID_696154928 m1A Human chr21 + 43577861 43577861 43577861 CCTTATGACAATACACCCTCCCTGCCCTTGCGATAATGGACTCTGTGATATTCCCCTGCCCTTAA CCTTATGACAATACACCCTCCCTGCCCTTGCGGTAATGGACTCTGTGATATTCCCCTGCCCTTAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43577845..43577928 26863196 MeRIP-seq:(Medium) rs1568880566 Functional Loss SNV dbSNP153 33..33 33 - - - 62035 RMVar_ID_62035 Human_SNP_ID_696162025 m1A Human chr21 + 43605134 43605134 43605134 CACACACATCACACACACACCACACAGATACCACACACACATCAGACACACCACACACACACCAG CACACACATCACACACACACCACACAGATACCGCACACACATCAGACACACCACACACACACCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43604253..43605373 26863196 MeRIP-seq:(Medium) rs1310198654 Functional Loss SNV dbSNP153 33..33 33 - - - 62036 RMVar_ID_62036 Human_SNP_ID_696184970 m1A Human chr21 + 43694116 43694116 43694116 GAGCCCAGCGCAGCCCCCGGCTCTTACCCAGGACCCCGCCCCGTGCTGAGCCTTCTGCTGAGGTC GAGCCCAGCGCAGCCCCCGGCTCTTACCCAGGGCCCCGCCCCGTGCTGAGCCTTCTGCTGAGGTC A G RRP1B Ensembl:ENSG00000160208 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43694065..43694232 26863196 MeRIP-seq:(Medium) rs943075432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573106,Human_RBP_ID_2705656,Human_RBP_ID_7050655,Human_RBP_ID_8859989,Human_RBP_ID_14327532,Human_RBP_ID_17284312,Human_RBP_ID_17514039,Human_RBP_ID_17980384,Human_RBP_ID_26495308,Human_RBP_ID_27302171 Human_miRNA_ID_254896,Human_miRNA_ID_2041750,Human_miRNA_ID_2041751,Human_miRNA_ID_2147569,Human_miRNA_ID_2147570,Human_miRNA_ID_2270703,Human_miRNA_ID_2270704,Human_miRNA_ID_2387568,Human_miRNA_ID_2387569,Human_miRNA_ID_2389041,Human_miRNA_ID_2389042,Human_miRNA_ID_2400190,Human_miRNA_ID_2400191,Human_miRNA_ID_2988996,Human_miRNA_ID_2988997,Human_miRNA_ID_3020728,Human_miRNA_ID_3020729,Human_miRNA_ID_3022698,Human_miRNA_ID_3022699,Human_miRNA_ID_3031253,Human_miRNA_ID_3031254 RMVar_hsa_circ_95467,RMVar_hsa_circ_212491,RMVar_hsa_circ_101963,RMVar_hsa_circ_91467,RMVar_hsa_circ_212501,RMVar_hsa_circ_212504 62037 RMVar_ID_62037 Human_SNP_ID_696185124 m1A Human chr21 + 43694665 43694665 43694665 CCAGCCACGCTCTGCTCAGGCCTGGAAGTGAAAGCCGCCTCCTTCCCGTTATGCCCCCCATACAG CCAGCCACGCTCTGCTCAGGCCTGGAAGTGAAGGCCGCCTCCTTCCCGTTATGCCCCCCATACAG A G RRP1B Ensembl:ENSG00000160208 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43694618..43694730 26863196 MeRIP-seq:(Medium) rs575037458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573114,Human_RBP_ID_17980390,Human_RBP_ID_18326828,Human_RBP_ID_27302180 RMVar_hsa_circ_95467,RMVar_hsa_circ_212491,RMVar_hsa_circ_101963,RMVar_hsa_circ_91467,RMVar_hsa_circ_212501,RMVar_hsa_circ_212504 62038 RMVar_ID_62038 Human_SNP_ID_696191802 m1A Human chr21 + 43719299 43719296 43719299 GCCCCGCGCCGCCGCGGCCAGGCCCGGCATGGAGGAGGAGTGCCGGGTGCTCTCCATACAGAGCC GCCCCGCGCCGCCGCGGCCAGGCCCGGCAT___GGAGGAGTGCCGGGTGCTCTCCATACAGAGCC TGGA T PDXK Ensembl:ENSG00000160209 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:43719126..43719581 26863196 MeRIP-seq:(Medium) rs1468389787 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4674649,Human_RBP_ID_8860898,Human_RBP_ID_22454136 Human_Splice_Rec_2127851,Human_Splice_Rec_2127855,Human_Splice_Rec_2127873,Human_Splice_Rec_2127893,Human_Splice_Rec_2127907,Human_Splice_Rec_2127909 62039 RMVar_ID_62039 Human_SNP_ID_696192450 m1A Human chr21 + 43721931 43721931 43721931 AGCCTAAGGTACATATTAGTGGTGGGGAACTAAAGGAGGGAACATGTTGGCATGACCAGTACTGG AGCCTAAGGTACATATTAGTGGTGGGGAACTAGAGGAGGGAACATGTTGGCATGACCAGTACTGG A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43721922..43722063 26863196 MeRIP-seq:(Medium) rs1342777586 Functional Loss SNV dbSNP153 33..33 33 - - - 62040 RMVar_ID_62040 Human_SNP_ID_696194085 m1A Human chr21 + 43727723 43727723 43727723 GGGAGGGAGCCAGCACTAGGTGGAGCTCTGCCAGCCGGGGCACAGGGAGGAACAGCATCCAGGAG GGGAGGGAGCCAGCACTAGGTGGAGCTCTGCCGGCCGGGGCACAGGGAGGAACAGCATCCAGGAG A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43727719..43727806 26863196 MeRIP-seq:(Medium) rs569483808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3665372,Human_RBP_ID_5652841,Human_RBP_ID_8116023 62041 RMVar_ID_62041 Human_SNP_ID_696194623 m1A Human chr21 - 43729457 43729457 43729457 CACCACTCTGTGAACTCCTCACTGGGCTGCAGAACCCCGGGCACCTTCTGAATCCTGTAAAGCTC CACCACTCTGTGAACTCCTCACTGGGCTGCAGTACCCCGGGCACCTTCTGAATCCTGTAAAGCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43729449..43729720 26863196 MeRIP-seq:(Medium) rs1229751222 Functional Loss SNV dbSNP153 33..33 33 - - - 62042 RMVar_ID_62042 Human_SNP_ID_696195187 m1A Human chr21 + 43731740 43731740 43731740 TCTGTCCTTGGCTCCCTTGTGGGTGGGGAAAGATGAGGTGTATCAGGCAGGGTCCAGTCCAGAAA TCTGTCCTTGGCTCCCTTGTGGGTGGGGAAAGGTGAGGTGTATCAGGCAGGGTCCAGTCCAGAAA A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43731732..43731871 26863196 MeRIP-seq:(Medium) rs537217688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5202423 62043 RMVar_ID_62043 Human_SNP_ID_696195956 m1A Human chr21 - 43734033 43734031 43734033 CAAGACAGAGAAGGAACAGGTAGGCGTAAGAGAGCCAGGTCTGGGGTCCCACGAACCCCAGCAGG CAAGACAGAGAAGGAACAGGTAGGCGTAAGAG__CCAGGTCTGGGGTCCCACGAACCCCAGCAGG GCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43734030..43734340 26863196 MeRIP-seq:(Medium) rs773199133 Functional Loss DEL dbSNP153 33..34 33 - - - 62044 RMVar_ID_62044 Human_SNP_ID_696195977 m1A Human chr21 - 43734055 43734054 43734056 CAATCTCAAATCCCAAAACCTGCAAGACAGAGAAGGAACAGGTAGGCGTAAGAGAGCCAGGTCTG CAATCTCAAATCCCAAAACCTGCAAGACAGA__AGGAACAGGTAGGCGTAAGAGAGCCAGGTCTG TTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43734051..43734321 26863196 MeRIP-seq:(Medium) rs1490031843 Functional Loss DEL dbSNP153 32..33 33 - - - 62045 RMVar_ID_62045 Human_SNP_ID_696202310 m1A Human chr21 - 43752504 43752504 43752504 AGTGCAGCATGTCCATCACCTAGCAGTGGCACAGGGAGCGTCAGCCACGGCCGGTCACATGTCAG AGTGCAGCATGTCCATCACCTAGCAGTGGCACGGGGAGCGTCAGCCACGGCCGGTCACATGTCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43752501..43752550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 62046 RMVar_ID_62046 Human_SNP_ID_696203539 m1A Human chr21 - 43756408 43756408 43756408 CGCGACACGGCCTCTGTACGGTAGTGGCAGCCAGGGCCCACTCGAGGCTCCACACGCAGCAGGCT CGCGACACGGCCTCTGTACGGTAGTGGCAGCCGGGGCCCACTCGAGGCTCCACACGCAGCAGGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43756360..43756541 26863196 MeRIP-seq:(Medium) rs916027785 Functional Loss SNV dbSNP153 33..33 33 - - - 62047 RMVar_ID_62047 Human_SNP_ID_696203690 m1A Human chr21 - 43756891 43756887 43756892 AGTGCTCAGCCTGCTGCACCACGGATGAGGGGAGCTTCCACAAGGAACCTGACGGGGTGGTTCTC AGTGCTCAGCCTGCTGCACCACGGATGAGGG_____TCCACAAGGAACCTGACGGGGTGGTTCTC AAGCTC A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:43756851..43756900 26863196 MeRIP-seq:(Medium) rs762672176 Functional Loss DEL dbSNP153 32..36 33 - - - 62048 RMVar_ID_62048 Human_SNP_ID_696204673 m1A Human chr21 + 43760526 43760526 43760526 TAGACAGCACCTCAGTTTCTGACTCCAGCCGCACACCTCCTGCCTCTGCCAGCAGGGGTTGCCGC TAGACAGCACCTCAGTTTCTGACTCCAGCCGCCCACCTCCTGCCTCTGCCAGCAGGGGTTGCCGC A C PDXK Ensembl:ENSG00000160209 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:43760476..43760550 26863196 MeRIP-seq:(Medium) rs1001488615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780375,Human_RBP_ID_14329023,Human_RBP_ID_18781995 RMVar_hsa_circ_124794,RMVar_hsa_circ_102532,RMVar_hsa_circ_212517,RMVar_hsa_circ_92105,RMVar_hsa_circ_212518,RMVar_hsa_circ_91067,RMVar_hsa_circ_212520,RMVar_hsa_circ_212521 62049 RMVar_ID_62049 Human_SNP_ID_696208463 m1A Human chr21 + 43774099 43774099 43774099 CAGAATCCTGCCCCTTCCACCCCAAGGGGCACAGCCCGGAGATGAAGCTTATTTTAGGATCACAA CAGAATCCTGCCCCTTCCACCCCAAGGGGCACGGCCCGGAGATGAAGCTTATTTTAGGATCACAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43774048..43774209 26863196 MeRIP-seq:(Medium) rs1028085696 Functional Loss SNV dbSNP153 33..33 33 - - - 62050 RMVar_ID_62050 Human_SNP_ID_696208502 m1A Human chr21 - 43774213 43774213 43774213 ACCAGACCAACAAAGCCAAGCATGATGAGCTGACCTATTTCTGATCCTGACTTTGGACAAGGCCC ACCAGACCAACAAAGCCAAGCATGATGAGCTGGCCTATTTCTGATCCTGACTTTGGACAAGGCCC T C CSTB Ensembl:ENSG00000160213 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs773945210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573228,Human_RBP_ID_1028137,Human_RBP_ID_1605483,Human_RBP_ID_1938067,Human_RBP_ID_3663773,Human_RBP_ID_8543394,Human_RBP_ID_14329268,Human_RBP_ID_17284579,Human_RBP_ID_17397798,Human_RBP_ID_17659726,Human_RBP_ID_22454137,Human_RBP_ID_22818771,Human_RBP_ID_23929547,Human_RBP_ID_24493364,Human_RBP_ID_26821820,Human_RBP_ID_27028720,Human_RBP_ID_27302281 Human_miRNA_ID_2213291,Human_miRNA_ID_2568716 RMVar_hsa_circ_80840,RMVar_hsa_circ_212522 62051 RMVar_ID_62051 Human_SNP_ID_696208711 m1A Human chr21 + 43774753 43774753 43774753 GAACTTCTTGTTTTCTTTCTCTTCAAGCTGGGACCTCACCTAGACAGAAGGGACAGAATGAGGAT GAACTTCTTGTTTTCTTTCTCTTCAAGCTGGGGCCTCACCTAGACAGAAGGGACAGAATGAGGAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr21:43774625..43774805;chr21:43774651..43774802;chr21:43774676..43774851 26863196,32194978 MeRIP-seq:(Medium) rs772315538 Functional Loss SNV dbSNP153 33..33 33 - - - 62052 RMVar_ID_62052 Human_SNP_ID_696208712 m1A Human chr21 + 43774753 43774753 43774753 GAACTTCTTGTTTTCTTTCTCTTCAAGCTGGGACCTCACCTAGACAGAAGGGACAGAATGAGGAT GAACTTCTTGTTTTCTTTCTCTTCAAGCTGGGTCCTCACCTAGACAGAAGGGACAGAATGAGGAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr21:43774625..43774805;chr21:43774651..43774802;chr21:43774676..43774851 26863196,32194978 MeRIP-seq:(Medium) rs772315538 Functional Loss SNV dbSNP153 33..33 33 - - - 62053 RMVar_ID_62053 Human_SNP_ID_696208981 m1A Human chr21 - 43775788 43775788 43775788 CTCCACGGTGATCCGATAGCAAGCGGGTGGGAAGGGTCTGGCTAAACTGACTTAGCCAGGCTTCT CTCCACGGTGATCCGATAGCAAGCGGGTGGGATGGGTCTGGCTAAACTGACTTAGCCAGGCTTCT T A CSTB Ensembl:ENSG00000160213 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43775784..43775898 26863196 MeRIP-seq:(Medium) rs1391181299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80840,RMVar_hsa_circ_212522 62054 RMVar_ID_62054 Human_SNP_ID_696209156 m1A Human chr21 + 43776263 43776263 43776263 GGTGGCCGGCTGCGTGGCGGAGGGCGCCCCGCACATCATCTTGGCGGCGACGGAGGGAATCTGGC GGTGGCCGGCTGCGTGGCGGAGGGCGCCCCGCCCATCATCTTGGCGGCGACGGAGGGAATCTGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:43776148..43776549;chr21:43776132..43776422 26863196 MeRIP-seq:(Medium) rs938561596 Functional Loss SNV dbSNP153 33..33 33 - - - 62055 RMVar_ID_62055 Human_SNP_ID_696209158 m1A Human chr21 + 43776268 43776268 43776268 CCGGCTGCGTGGCGGAGGGCGCCCCGCACATCATCTTGGCGGCGACGGAGGGAATCTGGCGAGGG CCGGCTGCGTGGCGGAGGGCGCCCCGCACATCGTCTTGGCGGCGACGGAGGGAATCTGGCGAGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:43776151..43776325 26863196 MeRIP-seq:(Medium) rs777803544 Functional Loss SNV dbSNP153 33..33 33 - - - 62056 RMVar_ID_62056 Human_SNP_ID_696209168 m1A Human chr21 - 43776304 43776292 43776305 TTGGGCTGAGGAGCCGCCGCGTCCCCTCGCCGAGTCCCCTCGCCAGATTCCCTCCGTCGCCGCCA TTGGGCTGAGGAGCCGCCGCGTCCCCTCGCC_____________AGATTCCCTCCGTCGCCGCCA TGGCGAGGGGACTC T CSTB Ensembl:ENSG00000160213 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:43776173..43776313 26863410 MeRIP-seq:(Medium) rs577227536 Functional Loss DEL dbSNP153,HGVD 32..44 33 - - - Human_RBP_ID_150982,Human_RBP_ID_573244,Human_RBP_ID_1381567,Human_RBP_ID_4675000,Human_RBP_ID_22533744,Human_RBP_ID_26822078 Human_miRNA_ID_2018133 RMVar_hsa_circ_80840,RMVar_hsa_circ_212522 62057 RMVar_ID_62057 Human_SNP_ID_696209179 m1A Human chr21 + 43776302 43776302 43776302 CTTGGCGGCGACGGAGGGAATCTGGCGAGGGGACTCGGCGAGGGGACGCGGCGGCTCCTCAGCCC CTTGGCGGCGACGGAGGGAATCTGGCGAGGGGCCTCGGCGAGGGGACGCGGCGGCTCCTCAGCCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:43776172..43776450 26863410 MeRIP-seq:(Medium) rs770366711 Functional Loss SNV dbSNP153 33..33 33 - - - 62058 RMVar_ID_62058 Human_SNP_ID_696209180 m1A Human chr21 + 43776302 43776302 43776302 CTTGGCGGCGACGGAGGGAATCTGGCGAGGGGACTCGGCGAGGGGACGCGGCGGCTCCTCAGCCC CTTGGCGGCGACGGAGGGAATCTGGCGAGGGGGCTCGGCGAGGGGACGCGGCGGCTCCTCAGCCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:43776172..43776450 26863410 MeRIP-seq:(Medium) rs770366711 Functional Loss SNV dbSNP153 33..33 33 - - - 62059 RMVar_ID_62059 Human_SNP_ID_696213241 m1A Human chr21 - 43789634 43789634 43789634 GCTGGATCTCAGGCGGGAGCTGCACGCGCGAAACCATGACGCCGACGGCCGAGACCCCCTGTCCC GCTGGATCTCAGGCGGGAGCTGCACGCGCGAAGCCATGACGCCGACGGCCGAGACCCCCTGTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:43789551..43789801;chr21:43789526..43789818 26863196 MeRIP-seq:(Medium) rs1452399333 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 62060 RMVar_ID_62060 Human_SNP_ID_696213247 m1A Human chr21 - 43789643 43789643 43789643 GCTGAGCCAGCTGGATCTCAGGCGGGAGCTGCACGCGCGAAACCATGACGCCGACGGCCGAGACC GCTGAGCCAGCTGGATCTCAGGCGGGAGCTGCGCGCGCGAAACCATGACGCCGACGGCCGAGACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43789551..43790540 26863196 MeRIP-seq:(Medium) rs1449005912 Functional Loss SNV dbSNP153 33..33 33 - - - 62061 RMVar_ID_62061 Human_SNP_ID_696213638 m1A Human chr21 - 43790989 43790989 43790989 GTTAATCTGTTGGTGATAATTCATCCAGCATTATACTGAGGGCTTCTGCACTCTCCTGTAATATA GTTAATCTGTTGGTGATAATTCATCCAGCATTGTACTGAGGGCTTCTGCACTCTCCTGTAATATA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43790983..43791450 26863196 MeRIP-seq:(Medium) rs1358378642 Functional Loss SNV dbSNP153 33..33 33 - - - 62062 RMVar_ID_62062 Human_SNP_ID_696213763 m1A Human chr21 + 43791362 43791357 43791363 CCGTTGCTGTTTTGATGCAGGTGGTTTTACGCACGACGAGCTGCTGAAGGTGTGGAAAGGACTGT CCGTTGCTGTTTTGATGCAGGTGGTTTT______GACGAGCTGCTGAAGGTGTGGAAAGGACTGT TACGCAC T RRP1 Ensembl:ENSG00000160214 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43791351..43791450 26863196 MeRIP-seq:(Medium) rs1424185436 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_4682604,Human_RBP_ID_14329402,Human_RBP_ID_18782019,Human_RBP_ID_22602619,Human_RBP_ID_23929559 Human_Splice_Rec_2128066,Human_Splice_Rec_2128067,Human_Splice_Rec_2128078,Human_Splice_Rec_2128079,Human_Splice_Rec_2128092,Human_Splice_Rec_2128093,Human_Splice_Rec_2128096,Human_Splice_Rec_2128097,Human_Splice_Rec_2128120 RMVar_hsa_circ_98709,RMVar_hsa_circ_212523 62063 RMVar_ID_62063 Human_SNP_ID_696215587 m1A Human chr21 - 43797538 43797538 43797538 CGTCGGAGCCCAGCCTCACCTCCTCGGCGCCCACTTTGGTCAGCTCCTCCAGGAAGATCTCGATG CGTCGGAGCCCAGCCTCACCTCCTCGGCGCCCGCTTTGGTCAGCTCCTCCAGGAAGATCTCGATG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:43795223..43797921 32194978 MeRIP-seq:(Medium) rs1569015365 Functional Loss SNV dbSNP153 33..33 33 - - - 62064 RMVar_ID_62064 Human_SNP_ID_696215596 m1A Human chr21 + 43797550 43797550 43797550 CCTGGAGGAGCTGACCAAAGTGGGCGCCGAGGAGGTGAGGCTGGGCTCCGACGGGGCGGTGGAGC CCTGGAGGAGCTGACCAAAGTGGGCGCCGAGGCGGTGAGGCTGGGCTCCGACGGGGCGGTGGAGC A C RRP1 Ensembl:ENSG00000160214 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43797527..43797622 26863196 MeRIP-seq:(Medium) rs764549852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928210,Human_RBP_ID_9391538,Human_RBP_ID_19007155,Human_RBP_ID_19110846,Human_RBP_ID_26344394 Human_Splice_Rec_2128087,Human_Splice_Rec_2128105,Human_Splice_Rec_2128125,Human_Splice_Rec_2128139 RMVar_hsa_circ_30766,RMVar_hsa_circ_98709,RMVar_hsa_circ_212523,RMVar_hsa_circ_212526,RMVar_hsa_circ_91899,RMVar_hsa_circ_364247,RMVar_hsa_circ_47254,RMVar_hsa_circ_79467,RMVar_hsa_circ_70958,RMVar_hsa_circ_212527 62065 RMVar_ID_62065 Human_SNP_ID_696215799 m1A Human chr21 + 43798026 43798026 43798026 ACTGGACACACAGGATGAGGAGGTGGCGTCGGACAGTGATGAGTCCTCTGAGGGTGGTGAGCGTG ACTGGACACACAGGATGAGGAGGTGGCGTCGGGCAGTGATGAGTCCTCTGAGGGTGGTGAGCGTG A G RRP1 Ensembl:ENSG00000160214 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43797890..43798028 26863196 MeRIP-seq:(Medium) rs371358839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4675041,Human_RBP_ID_14329738,Human_RBP_ID_19007158,Human_RBP_ID_27820729 Human_Splice_Rec_2128109,Human_Splice_Rec_2128129,Human_Splice_Rec_2128143 RMVar_hsa_circ_30766,RMVar_hsa_circ_98709,RMVar_hsa_circ_212523,RMVar_hsa_circ_212526,RMVar_hsa_circ_91899,RMVar_hsa_circ_364247,RMVar_hsa_circ_47254,RMVar_hsa_circ_79467,RMVar_hsa_circ_70958,RMVar_hsa_circ_212527 62066 RMVar_ID_62066 Human_SNP_ID_696235481 m1A Human chr21 + 43864426 43864426 43864426 TGGGGCTGAGAGGGCTCCGCGGTCTGGAGGGGACGGCGTCAGCGCCCGCGGGGGTTCGCAGGGCA TGGGGCTGAGAGGGCTCCGCGGTCTGGAGGGGGCGGCGTCAGCGCCCGCGGGGGTTCGCAGGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43864375..43864571 26863196 MeRIP-seq:(Medium) rs1323878369 Functional Loss SNV dbSNP153 33..33 33 - - - 62067 RMVar_ID_62067 Human_SNP_ID_696245144 m1A Human chr21 + 43900397 43900397 43900397 GCATGAAGCCACAGGCTTCAGACACTGGTGGCAGGCCGTGTGGACAGTGACCAGAGAGGGGCATG GCATGAAGCCACAGGCTTCAGACACTGGTGGCGGGCCGTGTGGACAGTGACCAGAGAGGGGCATG A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43900394..43900509 26863196 MeRIP-seq:(Medium) rs541854459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14332589 RMVar_hsa_circ_109762,RMVar_hsa_circ_212528 62068 RMVar_ID_62068 Human_SNP_ID_696246033 m1A Human chr21 - 43903919 43903919 43903919 AGTGAAAGGCACACATGTCAACGTGCTTGCGCAGGACTGGAGAGACGCCGTGTGACCAAATATAT AGTGAAAGGCACACATGTCAACGTGCTTGCGCTGGACTGGAGAGACGCCGTGTGACCAAATATAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43903915..43904060 26863196 MeRIP-seq:(Medium) rs541958704 Functional Loss SNV dbSNP153 33..33 33 - - - 62069 RMVar_ID_62069 Human_SNP_ID_696246034 m1A Human chr21 - 43903919 43903919 43903919 AGTGAAAGGCACACATGTCAACGTGCTTGCGCAGGACTGGAGAGACGCCGTGTGACCAAATATAT AGTGAAAGGCACACATGTCAACGTGCTTGCGCGGGACTGGAGAGACGCCGTGTGACCAAATATAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43903915..43904060 26863196 MeRIP-seq:(Medium) rs541958704 Functional Loss SNV dbSNP153 33..33 33 - - - 62070 RMVar_ID_62070 Human_SNP_ID_696247943 m1A Human chr21 - 43910535 43910535 43910535 GGCCCTCCGCTCCACCTTCACCTCACTGTATTAGGACTTCACCTAATTCACTTAATTCACCTAAT GGCCCTCCGCTCCACCTTCACCTCACTGTATTTGGACTTCACCTAATTCACTTAATTCACCTAAT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:43910532..43910676 26863196 MeRIP-seq:(Medium) rs1267727522 Functional Loss SNV dbSNP153 33..33 33 - - - 62071 RMVar_ID_62071 Human_SNP_ID_696247946 m1A Human chr21 + 43910557 43910557 43910557 GGTGAAGTCCTAATACAGTGAGGTGAAGGTGGAGCGGAGGGCCGAGGAGGGCCGGCCTTCCCTCT GGTGAAGTCCTAATACAGTGAGGTGAAGGTGGGGCGGAGGGCCGAGGAGGGCCGGCCTTCCCTCT A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43910555..43910697 26863196 MeRIP-seq:(Medium) rs1426286915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17146046 RMVar_hsa_circ_14631 62072 RMVar_ID_62072 Human_SNP_ID_696247947 m1A Human chr21 + 43910557 43910557 43910557 GGTGAAGTCCTAATACAGTGAGGTGAAGGTGGAGCGGAGGGCCGAGGAGGGCCGGCCTTCCCTCT GGTGAAGTCCTAATACAGTGAGGTGAAGGTGGTGCGGAGGGCCGAGGAGGGCCGGCCTTCCCTCT A T AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43910555..43910697 26863196 MeRIP-seq:(Medium) rs1426286915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17146046 RMVar_hsa_circ_14631 62073 RMVar_ID_62073 Human_SNP_ID_696249988 m1A Human chr21 - 43918094 43918081 43918095 CACAACACCCATAACACAACACCCACAACACAACACCCACAACACCCACAACACCCACAACCCCA CACAACACCCATAACACAACACCCACAACAC______________CCACAACACCCACAACCCCA GGTGTTGTGGGTGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43918092..43918302 26863196 MeRIP-seq:(Medium) rs1396149077 Functional Loss DEL dbSNP153 32..45 33 - - - 62074 RMVar_ID_62074 Human_SNP_ID_696249995 m1A Human chr21 - 43918094 43918090 43918095 CACAACACCCATAACACAACACCCACAACACAACACCCACAACACCCACAACACCCACAACCCCA CACAACACCCATAACACAACACCCACAACAC_____CCACAACACCCACAACACCCACAACCCCA GGTGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43918092..43918302 26863196 MeRIP-seq:(Medium) rs1441485233 Functional Loss DEL dbSNP153 32..36 33 - - - 62075 RMVar_ID_62075 Human_SNP_ID_696250012 m1A Human chr21 - 43918120 43918120 43918120 CCCACAACTCCAACACCCACAACCCCCACAACACCCATAACACAACACCCACAACACAACACCCA CCCACAACTCCAACACCCACAACCCCCACAACCCCCATAACACAACACCCACAACACAACACCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43918112..43918302 26863196 MeRIP-seq:(Medium) rs892194951 Functional Loss SNV dbSNP153 33..33 33 - - - 62076 RMVar_ID_62076 Human_SNP_ID_696250013 m1A Human chr21 - 43918125 43918123 43918126 CAACACCCACAACTCCAACACCCACAACCCCCACAACACCCATAACACAACACCCACAACACAAC CAACACCCACAACTCCAACACCCACAACCCC___AACACCCATAACACAACACCCACAACACAAC TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43918119..43918286 26863196 MeRIP-seq:(Medium) rs1158160781 Functional Loss DEL dbSNP153 32..34 33 - - - 62077 RMVar_ID_62077 Human_SNP_ID_696250599 m1A Human chr21 - 43920232 43920229 43920233 TTACACACACCCTTACACACACACACTCACTCACAATCTCTCACACACACACACACAGGGCTGAA TTACACACACCCTTACACACACACACTCACT____ATCTCTCACACACACACACACAGGGCTGAA TTGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43920229..43920346 26863196 MeRIP-seq:(Medium) rs1373841144 Functional Loss DEL dbSNP153 32..35 33 - - - 62078 RMVar_ID_62078 Human_SNP_ID_696250608 m1A Human chr21 - 43920256 43920256 43920256 CTCTCACACTGACACATTCACGCTTTACACACACCCTTACACACACACACTCACTCACAATCTCT CTCTCACACTGACACATTCACGCTTTACACACCCCCTTACACACACACACTCACTCACAATCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43920253..43920347 26863196 MeRIP-seq:(Medium) rs889039691 Functional Loss SNV dbSNP153 33..33 33 - - - 62079 RMVar_ID_62079 Human_SNP_ID_696251175 m1A Human chr21 - 43922266 43922266 43922266 CATCCTCGCCTCGCCACCCCCACAAGAACAGGAGCCTCCTCCGTCACATCCACTCCTCGTCCCCA CATCCTCGCCTCGCCACCCCCACAAGAACAGGGGCCTCCTCCGTCACATCCACTCCTCGTCCCCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:43922243..43922356 26863196 MeRIP-seq:(Medium) rs1376363656 Functional Loss SNV dbSNP153 33..33 33 - - - 62080 RMVar_ID_62080 Human_SNP_ID_696259918 m1A Human chr21 + 43954289 43954289 43954289 TGCTGCCATTGGAGGTTTGTGCAGTCAGGTTTATCAAGGAGGTCCAGGCGGGCTGGGTGTGGGGA TGCTGCCATTGGAGGTTTGTGCAGTCAGGTTTCTCAAGGAGGTCCAGGCGGGCTGGGTGTGGGGA A C AP001054.1,AGPAT3 Ensembl:ENSG00000288593,Ensembl:ENSG00000160216 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43954284..43954412 26863196 MeRIP-seq:(Medium) rs1307136857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10119 RMVar_hsa_circ_14631 62081 RMVar_ID_62081 Human_SNP_ID_696261219 m1A Human chr21 - 43958557 43958555 43958558 ACACCACAAACCACACACACGCCACACGCACCACACACACCACAAACCACACCTACACCACACAC ACACCACAAACCACACACACGCCACACGCAC___ACACACCACAAACCACACCTACACCACACAC TGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43958555..43959451 26863196 MeRIP-seq:(Medium) rs759081172 Functional Loss DEL dbSNP153 32..34 33 - - - 62082 RMVar_ID_62082 Human_SNP_ID_696266053 m1A Human chr21 + 43974545 43974543 43974545 GTATAGTGTGTCATGTGGTGTGTGTGTAAATTATATGTGTGTGGTGTGTGTGTAGTGTGTGTATA GTATAGTGTGTCATGTGGTGTGTGTGTAAAT__TATGTGTGTGGTGTGTGTGTAGTGTGTGTATA TTA T AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43974540..43974734 26863196 MeRIP-seq:(Medium) rs570862935 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8949584 62083 RMVar_ID_62083 Human_SNP_ID_696266054 m1A Human chr21 + 43974545 43974545 43974545 GTATAGTGTGTCATGTGGTGTGTGTGTAAATTATATGTGTGTGGTGTGTGTGTAGTGTGTGTATA GTATAGTGTGTCATGTGGTGTGTGTGTAAATTGTATGTGTGTGGTGTGTGTGTAGTGTGTGTATA A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43974540..43974734 26863196 MeRIP-seq:(Medium) rs925056891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8949584 62084 RMVar_ID_62084 Human_SNP_ID_696266056 m1A Human chr21 - 43974559 43974547 43974560 ACCCTCACGATTTATATACACACACTACACACACACCACACACATATAATTTACACACACACCAC ACCCTCACGATTTATATACACACACTACACA_____________TATAATTTACACACACACCAC ATGTGTGTGGTGTG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43974552..43974737 26863196 MeRIP-seq:(Medium) rs371869848 Functional Loss DEL dbSNP153 32..44 33 - - - 62085 RMVar_ID_62085 Human_SNP_ID_696266057 m1A Human chr21 - 43974559 43974547 43974560 ACCCTCACGATTTATATACACACACTACACACACACCACACACATATAATTTACACACACACCAC ACCCTCACGATTTATATACACACACTACACA___________CATATAATTTACACACACACCAC ATGTGTGTGGTGTG ATG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43974552..43974737 26863196 MeRIP-seq:(Medium) rs371869848 Functional Loss DEL dbSNP153 32..42 33 - - - 62086 RMVar_ID_62086 Human_SNP_ID_696266064 m1A Human chr21 - 43974559 43974559 43974559 ACCCTCACGATTTATATACACACACTACACACACACCACACACATATAATTTACACACACACCAC ACCCTCACGATTTATATACACACACTACACACTCACCACACACATATAATTTACACACACACCAC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:43974552..43974737 26863196 MeRIP-seq:(Medium) rs1221313533 Functional Loss SNV dbSNP153 33..33 33 - - - 62087 RMVar_ID_62087 Human_SNP_ID_696266236 m1A Human chr21 - 43975207 43975207 43975207 CCAAAACATTACCACACACCAGCACACACCAGAACACACCACACGTTAGCACATGCCATACACCA CCAAAACATTACCACACACCAGCACACACCAGCACACACCACACGTTAGCACATGCCATACACCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43975199..43975282 26863196 MeRIP-seq:(Medium) rs535764850 Functional Loss SNV dbSNP153 33..33 33 - - - 62088 RMVar_ID_62088 Human_SNP_ID_696268558 m1A Human chr21 + 43983477 43983477 43983477 CACCCCCCAGCCTCGCACTGTGTCCTTGGGGAAGGCCCGCCCCCATCCTGGCCGGTGTCACTGTG CACCCCCCAGCCTCGCACTGTGTCCTTGGGGAGGGCCCGCCCCCATCCTGGCCGGTGTCACTGTG A G AGPAT3 Ensembl:ENSG00000160216 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:43983436..43983537 32194978 MeRIP-seq:(Medium) rs11537799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8206334 62089 RMVar_ID_62089 Human_SNP_ID_696268848 m1A Human chr21 + 43984457 43984457 43984457 AAATGCAAATTTAGATCTTTTATGATTTAATTATTATTGTTTCCCATAGAAGTTCCCTCCCTTTG AAATGCAAATTTAGATCTTTTATGATTTAATTGTTATTGTTTCCCATAGAAGTTCCCTCCCTTTG A G AGPAT3 Ensembl:ENSG00000160216 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2706073,Human_RBP_ID_3663938,Human_RBP_ID_4675430,Human_RBP_ID_7051376 Human_miRNA_ID_1087421 GWAS_ID_7603,GWAS_ID_7604,GWAS_ID_7605,GWAS_ID_7606,GWAS_ID_7607,GWAS_ID_7608,GWAS_ID_7609,GWAS_ID_7610,GWAS_ID_7611,GWAS_ID_7612,GWAS_ID_7613,GWAS_ID_7614,GWAS_ID_7615,GWAS_ID_7616 62090 RMVar_ID_62090 Human_SNP_ID_696276798 m1A Human chr21 - 44012456 44012456 44012456 TCCGGCGTCACCGGCCCGGCCCCCCGCGCCCCATGGGCAGCCCCGAGGCCGCGCCGGGCCCAGCC TCCGGCGTCACCGGCCCGGCCCCCCGCGCCCCTTGGGCAGCCCCGAGGCCGCGCCGGGCCCAGCC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr21:44012368..44012519 26863410 MeRIP-seq:(Medium) rs1442780016 Functional Loss SNV dbSNP153 33..33 33 - - - 62091 RMVar_ID_62091 Human_SNP_ID_696282782 m1A Human chr21 + 44034054 44034054 44034054 AGGCAGACGTGCATAAAGACAGAGAAAGGAGGAGGCAGCGGAGGCCGCAGGATATAGCTGTGTTT AGGCAGACGTGCATAAAGACAGAGAAAGGAGGGGGCAGCGGAGGCCGCAGGATATAGCTGTGTTT A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44034017..44034119 26863196 MeRIP-seq:(Medium) rs1159988842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22525441 RMVar_hsa_circ_212533,RMVar_hsa_circ_84902,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_59795,RMVar_hsa_circ_302945,RMVar_hsa_circ_345151,RMVar_hsa_circ_347561,RMVar_hsa_circ_60251,RMVar_hsa_circ_212535 62092 RMVar_ID_62092 Human_SNP_ID_696283741 m1A Human chr21 + 44037843 44037843 44037843 AAGATGATTCACCTAGAGTCTAACTTTGTTCAATTCAAAGAGGAGCTGCTGCCCAAAGAAGGAAA AAGATGATTCACCTAGAGTCTAACTTTGTTCAGTTCAAAGAGGAGCTGCTGCCCAAAGAAGGAAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs114309802 Functional Loss SNV dbSNP153 33..33 33 - - - 62093 RMVar_ID_62093 Human_SNP_ID_696283778 m1A Human chr21 - 44037964 44037964 44037964 TCACACAGCACTCTCCACGCATCTCCAACCCCATCCCACCGCGCATCCTCTTCCCCTGCTGGTAC TCACACAGCACTCTCCACGCATCTCCAACCCCTTCCCACCGCGCATCCTCTTCCCCTGCTGGTAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44037963..44038056 26863196 MeRIP-seq:(Medium) rs771129889 Functional Loss SNV dbSNP153 33..33 33 - - - 62094 RMVar_ID_62094 Human_SNP_ID_696289116 m1A Human chr21 + 44058151 44058151 44058151 GTGACGCATATGCTAGGGCGAGAGAGAGGCACAAGGCAGAGATGGTGTGGGGTGCTGTGCGGGTC GTGACGCATATGCTAGGGCGAGAGAGAGGCACGAGGCAGAGATGGTGTGGGGTGCTGTGCGGGTC A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44058100..44058380;chr21:44058118..44058236 26863196 MeRIP-seq:(Medium) rs955389582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832740,Human_RBP_ID_14335969 RMVar_hsa_circ_212538,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_59795,RMVar_hsa_circ_345151,RMVar_hsa_circ_60251,RMVar_hsa_circ_338165,RMVar_hsa_circ_212535,RMVar_hsa_circ_328993,RMVar_hsa_circ_64013,RMVar_hsa_circ_212542,RMVar_hsa_circ_316196,RMVar_hsa_circ_356808,RMVar_hsa_circ_212537,RMVar_hsa_circ_362162,RMVar_hsa_circ_374841,RMVar_hsa_circ_326730,RMVar_hsa_circ_275141,RMVar_hsa_circ_309804,RMVar_hsa_circ_212540,RMVar_hsa_circ_212541,RMVar_hsa_circ_212539,RMVar_hsa_circ_212546,RMVar_hsa_circ_291882,RMVar_hsa_circ_324668,RMVar_hsa_circ_354574,RMVar_hsa_circ_359426,RMVar_hsa_circ_303531,RMVar_hsa_circ_212545 62095 RMVar_ID_62095 Human_SNP_ID_696289251 m1A Human chr21 - 44058692 44058692 44058692 GGCTCCGCCCTTGGACTTCCCTGTCTACACTCACTATTCCCTCTCCATGACGGAGCCCATCTACA GGCTCCGCCCTTGGACTTCCCTGTCTACACTCCCTATTCCCTCTCCATGACGGAGCCCATCTACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44058690..44058785 26863196 MeRIP-seq:(Medium) rs1182457629 Functional Loss SNV dbSNP153 33..33 33 - - - 62096 RMVar_ID_62096 Human_SNP_ID_696307942 m1A Human chr21 - 44133714 44133713 44133714 CAGATGCCGCAGCGAGCCTCGAGGCCACCAGGACCCTCACAGCCGCCATTGCGGTGAGGACAGCG CAGATGCCGCAGCGAGCCTCGAGGCCACCAGG_CCCTCACAGCCGCCATTGCGGTGAGGACAGCG GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44133676..44133770;chr21:44133687..44133761;chr21:44133687..44133783;chr21:44133690..44133776 26863196 MeRIP-seq:(Medium) rs763258982 Functional Loss DEL dbSNP153 33..33 33 - - - 62097 RMVar_ID_62097 Human_SNP_ID_696307945 m1A Human chr21 - 44133714 44133714 44133714 CAGATGCCGCAGCGAGCCTCGAGGCCACCAGGACCCTCACAGCCGCCATTGCGGTGAGGACAGCG CAGATGCCGCAGCGAGCCTCGAGGCCACCAGGGCCCTCACAGCCGCCATTGCGGTGAGGACAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44133676..44133770;chr21:44133687..44133761;chr21:44133687..44133783;chr21:44133690..44133776 26863196 MeRIP-seq:(Medium) rs968714 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7617,GWAS_ID_7618 62098 RMVar_ID_62098 Human_SNP_ID_696307956 m1A Human chr21 - 44133725 44133725 44133725 GGACGTGAATGCAGATGCCGCAGCGAGCCTCGAGGCCACCAGGACCCTCACAGCCGCCATTGCGG GGACGTGAATGCAGATGCCGCAGCGAGCCTCGGGGCCACCAGGACCCTCACAGCCGCCATTGCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:44133626..44133825 26863410 MeRIP-seq:(Medium) rs1446716322 Functional Loss SNV dbSNP153 33..33 33 - - - 62099 RMVar_ID_62099 Human_SNP_ID_696309291 m1A Human chr21 + 44139575 44139575 44139575 CAGGGGTCGCTGCTGCCTTCTAATTCAGTTCCAACAGTATGGACCCGGGGTAGCGTCCGATCGCA CAGGGGTCGCTGCTGCCTTCTAATTCAGTTCCGACAGTATGGACCCGGGGTAGCGTCCGATCGCA A G GATD3A Ensembl:ENSG00000160221 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4819377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7052048,Human_RBP_ID_14338895 RMVar_hsa_circ_78470,RMVar_hsa_circ_212572 62100 RMVar_ID_62100 Human_SNP_ID_696347600 m1A Human chr21 + 44299032 44299032 44299032 GGGCTGGTCTCGAACTCCTGACCTCAGACCTCAGGTGATCCACCCCCCCCCCCCCCCCCCACCCC GGGCTGGTCTCGAACTCCTGACCTCAGACCTCGGGTGATCCACCCCCCCCCCCCCCCCCCACCCC A G lnc-AIRE-2 RNACentral:URS00008B8A0A lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44299026..44299075 26863196 MeRIP-seq:(Medium) rs1352832046 Functional Loss SNV dbSNP153 33..33 33 - - - 62101 RMVar_ID_62101 Human_SNP_ID_696348096 m1A Human chr21 - 44300167 44300167 44300167 CCCGCCCACCTTGCGCGTCGCCGCCGCTGGTCAGGACGCCGATGGCCTTGCCCGCGCCCGACGCC CCCGCCCACCTTGCGCGTCGCCGCCGCTGGTCTGGACGCCGATGGCCTTGCCCGCGCCCGACGCC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:44300122..44300235 26863196 MeRIP-seq:(Medium) rs988201240 Functional Loss SNV dbSNP153 33..33 33 - - - 62102 RMVar_ID_62102 Human_SNP_ID_696350328 m1A Human chr21 + 44306630 44306624 44306630 ACCCCCTGTCCTCTGAGATGGGGAGGGTGTCCAGGGCCTTGCTTCTCAGCGTGGGACTGACAGGT ACCCCCTGTCCTCTGAGATGGGGAGGG______GGGCCTTGCTTCTCAGCGTGGGACTGACAGGT GTGTCCA G PFKL Ensembl:ENSG00000141959 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44306628..44306803 26863196 MeRIP-seq:(Medium) rs1251165625 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577 62103 RMVar_ID_62103 Human_SNP_ID_696351570 m1A Human chr21 + 44311043 44311043 44311043 TGAGGGCCTCGTGGAGGGAGGTGAGAACATCAAGCAGGCCAACTGGCTGAGCGTCTCCAACATCA TGAGGGCCTCGTGGAGGGAGGTGAGAACATCAGGCAGGCCAACTGGCTGAGCGTCTCCAACATCA A G PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44305902..44312344 26863196 MeRIP-seq:(Medium) rs1433758461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264872,Human_RBP_ID_1606133,Human_RBP_ID_4676077,Human_RBP_ID_5148635,Human_RBP_ID_5240611,Human_RBP_ID_5386890,Human_RBP_ID_26821834 Human_Splice_Rec_2128954,Human_Splice_Rec_2128955,Human_Splice_Rec_2128996,Human_Splice_Rec_2128997,Human_Splice_Rec_2129040,Human_Splice_Rec_2129041,Human_Splice_Rec_2129054,Human_Splice_Rec_2129055,Human_Splice_Rec_2129094,Human_Splice_Rec_2129095 Human_miRNA_ID_1094544 RMVar_hsa_circ_79964,RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577,RMVar_hsa_circ_320519,RMVar_hsa_circ_74862,RMVar_hsa_circ_212578 62104 RMVar_ID_62104 Human_SNP_ID_696351571 m1A Human chr21 + 44311043 44311043 44311043 TGAGGGCCTCGTGGAGGGAGGTGAGAACATCAAGCAGGCCAACTGGCTGAGCGTCTCCAACATCA TGAGGGCCTCGTGGAGGGAGGTGAGAACATCATGCAGGCCAACTGGCTGAGCGTCTCCAACATCA A T PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44305902..44312344 26863196 MeRIP-seq:(Medium) rs1433758461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264872,Human_RBP_ID_1606133,Human_RBP_ID_4676077,Human_RBP_ID_5148635,Human_RBP_ID_5240611,Human_RBP_ID_5386890,Human_RBP_ID_26821834 Human_Splice_Rec_2128954,Human_Splice_Rec_2128955,Human_Splice_Rec_2128996,Human_Splice_Rec_2128997,Human_Splice_Rec_2129040,Human_Splice_Rec_2129041,Human_Splice_Rec_2129054,Human_Splice_Rec_2129055,Human_Splice_Rec_2129094,Human_Splice_Rec_2129095 Human_miRNA_ID_1094544 RMVar_hsa_circ_79964,RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577,RMVar_hsa_circ_320519,RMVar_hsa_circ_74862,RMVar_hsa_circ_212578 62105 RMVar_ID_62105 Human_SNP_ID_696352050 m1A Human chr21 - 44312174 44312174 44312174 CAGGTTGGTGATGCCGTGCTGGACCAGGTTGTAGGCCGCTGCCCGGCGCCCCTCCCTGGTGGTAA CAGGTTGGTGATGCCGTGCTGGACCAGGTTGTGGGCCGCTGCCCGGCGCCCCTCCCTGGTGGTAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44312126..44312225 26863196 MeRIP-seq:(Medium) rs1371867936 Functional Loss SNV dbSNP153 33..33 33 - - - 62106 RMVar_ID_62106 Human_SNP_ID_696352596 m1A Human chr21 - 44313684 44313684 44313684 GGGCCACCCAGCGGGCCAGGAAGCCCCTCCTCACCCGCAGTGCCGGCCCATCACTTCCAGCACGA GGGCCACCCAGCGGGCCAGGAAGCCCCTCCTCGCCCGCAGTGCCGGCCCATCACTTCCAGCACGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44313676..44313700 26863196 MeRIP-seq:(Medium) rs764145950 Functional Loss SNV dbSNP153 33..33 33 - - - 62107 RMVar_ID_62107 Human_SNP_ID_696352705 m1A Human chr21 + 44313969 44313969 44313969 GGCCTCAGGGGCCGACTGGCTGTTCATCCCCGAGGCTCCACCCGAGGACGGCTGGGAGAACTTCA GGCCTCAGGGGCCGACTGGCTGTTCATCCCCGGGGCTCCACCCGAGGACGGCTGGGAGAACTTCA A G PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44313693..44314947 26863196 MeRIP-seq:(Medium) rs1316268323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1606137,Human_RBP_ID_18193871,Human_RBP_ID_19007181 Human_Splice_Rec_2128962,Human_Splice_Rec_2128963,Human_Splice_Rec_2129004,Human_Splice_Rec_2129005,Human_Splice_Rec_2129048,Human_Splice_Rec_2129049,Human_Splice_Rec_2129062,Human_Splice_Rec_2129102 Human_miRNA_ID_2209624,Human_miRNA_ID_3034230 RMVar_hsa_circ_52024,RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577,RMVar_hsa_circ_320519,RMVar_hsa_circ_74862,RMVar_hsa_circ_93789,RMVar_hsa_circ_212582,RMVar_hsa_circ_212581,RMVar_hsa_circ_32362 62108 RMVar_ID_62108 Human_SNP_ID_696352712 m1A Human chr21 + 44313984 44313984 44313984 CTGGCTGTTCATCCCCGAGGCTCCACCCGAGGACGGCTGGGAGAACTTCATGTGTGAGAGGCTGG CTGGCTGTTCATCCCCGAGGCTCCACCCGAGGTCGGCTGGGAGAACTTCATGTGTGAGAGGCTGG A T PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44313933..44314062 26863196 MeRIP-seq:(Medium) rs1057037 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5201849,Human_RBP_ID_14339998,Human_RBP_ID_18193871,Human_RBP_ID_18782586,Human_RBP_ID_19007181 Human_Splice_Rec_2128962,Human_Splice_Rec_2128963,Human_Splice_Rec_2129004,Human_Splice_Rec_2129005,Human_Splice_Rec_2129048,Human_Splice_Rec_2129049,Human_Splice_Rec_2129062,Human_Splice_Rec_2129102 GWAS_ID_7619,GWAS_ID_7620,GWAS_ID_7621,GWAS_ID_7622,GWAS_ID_7623,GWAS_ID_7624 RMVar_hsa_circ_52024,RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577,RMVar_hsa_circ_320519,RMVar_hsa_circ_74862,RMVar_hsa_circ_93789,RMVar_hsa_circ_212582,RMVar_hsa_circ_212581,RMVar_hsa_circ_32362 62109 RMVar_ID_62109 Human_SNP_ID_696352850 m1A Human chr21 + 44314377 44314377 44314377 GAGGTGGTTGGTTGTGAGGGAGTGGCCCCAGCAAGGTCCAGACGGCAGGGCTGTGGGGGTGGCGA GAGGTGGTTGGTTGTGAGGGAGTGGCCCCAGCGAGGTCCAGACGGCAGGGCTGTGGGGGTGGCGA A G PFKL Ensembl:ENSG00000141959 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44314028..44314865 26863196 MeRIP-seq:(Medium) rs900634988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_265170,Human_RBP_ID_1068512,Human_RBP_ID_3665419,Human_RBP_ID_3961698,Human_RBP_ID_5323534,Human_RBP_ID_5386070,Human_RBP_ID_8115674,Human_RBP_ID_8205801,Human_RBP_ID_8235204,Human_RBP_ID_8943031,Human_RBP_ID_9332183,Human_RBP_ID_9431895,Human_RBP_ID_17193419,Human_RBP_ID_18413038,Human_RBP_ID_18952036,Human_RBP_ID_21984581,Human_RBP_ID_22673116,Human_RBP_ID_22744176,Human_RBP_ID_26344745,Human_RBP_ID_27840806 RMVar_hsa_circ_52024,RMVar_hsa_circ_320519,RMVar_hsa_circ_93789,RMVar_hsa_circ_212581 62110 RMVar_ID_62110 Human_SNP_ID_696353100 m1A Human chr21 + 44315189 44315187 44315189 TAGGGCAGGGACTTCCCGGGGGTTCCGGCTCCAGTGGTGACCTTGGCCTTAGCTTATGTCTGTGA TAGGGCAGGGACTTCCCGGGGGTTCCGGCTC__GTGGTGACCTTGGCCTTAGCTTATGTCTGTGA CCA C PFKL Ensembl:ENSG00000141959 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44315185..44315313 26863196 MeRIP-seq:(Medium) rs1369156041 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10125,Human_RBP_ID_780117,Human_RBP_ID_3665429,Human_RBP_ID_5202179,Human_RBP_ID_5323537,Human_RBP_ID_5386518,Human_RBP_ID_8115682,Human_RBP_ID_8206341,Human_RBP_ID_8729346,Human_RBP_ID_9432145,Human_RBP_ID_18412995,Human_RBP_ID_18496311,Human_RBP_ID_21984586,Human_RBP_ID_22723520,Human_RBP_ID_22743990,Human_RBP_ID_23258431,Human_RBP_ID_23930383,Human_RBP_ID_27840946 RMVar_hsa_circ_52024,RMVar_hsa_circ_320519,RMVar_hsa_circ_93789,RMVar_hsa_circ_212581 62111 RMVar_ID_62111 Human_SNP_ID_696353683 m1A Human chr21 - 44316728 44316728 44316728 ACTGACACACACCCACACACACTGCCACACACACCCACACGGACCAGACACACACAGACACACCC ACTGACACACACCCACACACACTGCCACACACCCCCACACGGACCAGACACACACAGACACACCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:44316595..44316807 26863196 MeRIP-seq:(Medium) rs1237593400 Functional Loss SNV dbSNP153 33..33 33 - - - 62112 RMVar_ID_62112 Human_SNP_ID_696354585 m1A Human chr21 + 44319535 44319535 44319535 GGCCTGGGTCATCCTTCTAGGCACCGCGTCTGAAGATCGAGGGAGGAAGGGGCCTGCGGGTGGTA GGCCTGGGTCATCCTTCTAGGCACCGCGTCTGCAGATCGAGGGAGGAAGGGGCCTGCGGGTGGTA A C PFKL Ensembl:ENSG00000141959 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44319533..44319664 26863196 MeRIP-seq:(Medium) rs998742748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21984398 RMVar_hsa_circ_116584,RMVar_hsa_circ_371863,RMVar_hsa_circ_89128,RMVar_hsa_circ_212583,RMVar_hsa_circ_212584,RMVar_hsa_circ_212585,RMVar_hsa_circ_120542,RMVar_hsa_circ_212586 62113 RMVar_ID_62113 Human_SNP_ID_696355298 m1A Human chr21 - 44321816 44321816 44321816 ATCGTGCACCACGTATACTGTGTGTCCATGGGAGATGCCGGTCCGCACCGCCGAGCGCACGGCCG ATCGTGCACCACGTATACTGTGTGTCCATGGGCGATGCCGGTCCGCACCGCCGAGCGCACGGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44321766..44321903 26863196 MeRIP-seq:(Medium) rs754003768 Functional Loss SNV dbSNP153 33..33 33 - - - 62114 RMVar_ID_62114 Human_SNP_ID_696356047 m1A Human chr21 - 44323884 44323884 44323884 CCATGGCGGCATTTACAGCAGTGTCGGAGCCCAGGCTGAAGTCGGTGCCAGGGACGTTGTTGCTG CCATGGCGGCATTTACAGCAGTGTCGGAGCCCGGGCTGAAGTCGGTGCCAGGGACGTTGTTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44323770..44323969 26863196 MeRIP-seq:(Medium) rs1330537388 Functional Loss SNV dbSNP153 33..33 33 - - - 62115 RMVar_ID_62115 Human_SNP_ID_696356335 m1A Human chr21 + 44324609 44324609 44324609 GGCCACCGTGACTGGCATTGCTGTGGGGGCCGACGCCGCCTACGTCTTCGAGGACCCTTTCAACA GGCCACCGTGACTGGCATTGCTGTGGGGGCCGGCGCCGCCTACGTCTTCGAGGACCCTTTCAACA A G PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44324564..44324673 26863196 MeRIP-seq:(Medium) rs1309223074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9391803,Human_RBP_ID_19007212,Human_RBP_ID_22453913 Human_Splice_Rec_2128983,Human_Splice_Rec_2129025,Human_Splice_Rec_2129079,Human_Splice_Rec_2129117,Human_Splice_Rec_2129133,Human_Splice_Rec_2129159,Human_Splice_Rec_2129177,Human_Splice_Rec_2129191 RMVar_hsa_circ_116584,RMVar_hsa_circ_81422,RMVar_hsa_circ_212585,RMVar_hsa_circ_120542,RMVar_hsa_circ_212586,RMVar_hsa_circ_86240,RMVar_hsa_circ_212589,RMVar_hsa_circ_377735,RMVar_hsa_circ_48889,RMVar_hsa_circ_212590 62116 RMVar_ID_62116 Human_SNP_ID_696356970 m1A Human chr21 - 44326062 44326062 44326062 CAAAGTGAGGCCTCGGGTCGCACCCACCACCTACCCTTGCGGTAAACCTCGCGCAGCTTCTCCGA CAAAGTGAGGCCTCGGGTCGCACCCACCACCTGCCCTTGCGGTAAACCTCGCGCAGCTTCTCCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44326028..44326216 26863196 MeRIP-seq:(Medium) rs1338692048 Functional Loss SNV dbSNP153 33..33 33 - - - 62117 RMVar_ID_62117 Human_SNP_ID_696357265 m1A Human chr21 - 44326705 44326705 44326705 ACTGCTCCCGTGGCATGCGGTGCCTGTGCAGGACGGGGATGGGAGGATGATGGGGAGTCAGGGGT ACTGCTCCCGTGGCATGCGGTGCCTGTGCAGGGCGGGGATGGGAGGATGATGGGGAGTCAGGGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44326701..44326725 32194978 MeRIP-seq:(Medium) rs749525978 Functional Loss SNV dbSNP153 33..33 33 - - - 62118 RMVar_ID_62118 Human_SNP_ID_696357331 m1A Human chr21 + 44326827 44326827 44326827 CCGCCTACGTGTCAGGGGAGCTGGAGCACGTGACCCGCCGCACCCTGAGCATGGACAAGGGCTTC CCGCCTACGTGTCAGGGGAGCTGGAGCACGTGCCCCGCCGCACCCTGAGCATGGACAAGGGCTTC A C PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr21:44326777..44326877;chr21:44326776..44327326 32194978 MeRIP-seq:(Medium) rs750136662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780135,Human_RBP_ID_18193875,Human_RBP_ID_22453989,Human_RBP_ID_22533745,Human_RBP_ID_23212582,Human_RBP_ID_26821844,Human_RBP_ID_27490634 RMVar_hsa_circ_86240,RMVar_hsa_circ_212590 62119 RMVar_ID_62119 Human_SNP_ID_696358851 m1A Human chr21 + 44330847 44330847 44330847 CCACTCACCCTGCCCCTGTGGCTGCTCGAGGCATCCCTGGCTGAGAGGGAAGGAAACTGGCCCCG CCACTCACCCTGCCCCTGTGGCTGCTCGAGGCGTCCCTGGCTGAGAGGGAAGGAAACTGGCCCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44330818..44331217 32194978 MeRIP-seq:(Medium) rs745920377 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_212591 62120 RMVar_ID_62120 Human_SNP_ID_696362043 m1A Human chr21 + 44339206 44339206 44339206 CATCTTCCGCGTCAGCTTCATGGCGGCCGCCCAGGCCCGACCGGCGGGCGCCCCCGGCCTCCTGA CATCTTCCGCGTCAGCTTCATGGCGGCCGCCCGGGCCCGACCGGCGGGCGCCCCCGGCCTCCTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44339194..44339357;chr21:44339032..44339375;chr21:44339084..44339370 26863196 MeRIP-seq:(Medium) rs1275274505 Functional Loss SNV dbSNP153 33..33 33 - - - 62121 RMVar_ID_62121 Human_SNP_ID_696382184 m1A Human chr21 - 44406700 44406700 44406700 TGAGGTAGGAGTGGTAGACGGCCCCTCGGAACAGCCAGTCCACCCGGCGCTCGTTGTGGATGAGG TGAGGTAGGAGTGGTAGACGGCCCCTCGGAACGGCCAGTCCACCCGGCGCTCGTTGTGGATGAGG T C TRPM2-AS,TRPM2-AS:2,TRPM2-AS:3,TRPM2-AS:4 RNACentral:URS0000D5AB21,RNACentral:URS0000D5DFB3,RNACentral:URS0000D58436,RNACentral:URS0000D59512 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44406693..44407137 26863196 MeRIP-seq:(Medium) rs770445071 Functional Loss SNV dbSNP153 33..33 33 - - - 62122 RMVar_ID_62122 Human_SNP_ID_696382358 m1A Human chr21 + 44406951 44406951 44406951 CAGCTCCTGTGGCAGGAAGTAGAAGGGGCCCCACCAGGGGAGGGAGGAGGGGGGCCTGGTGGGGG CAGCTCCTGTGGCAGGAAGTAGAAGGGGCCCCGCCAGGGGAGGGAGGAGGGGGGCCTGGTGGGGG A G TRPM2 Ensembl:ENSG00000142185 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44406942..44407013 26863196 MeRIP-seq:(Medium) rs1046539401 Functional Loss SNV dbSNP153 33..33 33 - - - 62123 RMVar_ID_62123 Human_SNP_ID_696386688 m1A Human chr21 - 44419726 44419712 44419727 CTGCCATCATCACCATCAACATCACCACCACTACCATCACCACCACCATCACCACCACTTCCATT CTGCCATCATCACCATCAACATCACCACCAC_______________CATCACCACCACTTCCATT GGTGGTGGTGATGGTA G TRPM2-AS Ensembl:ENSG00000230061 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44419718..44419958 26863196 MeRIP-seq:(Medium) rs1325934027 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_207830,Human_RBP_ID_265180,Human_RBP_ID_2706339,Human_RBP_ID_24534176 62124 RMVar_ID_62124 Human_SNP_ID_696386697 m1A Human chr21 - 44419726 44419725 44419728 CTGCCATCATCACCATCAACATCACCACCACTACCATCACCACCACCATCACCACCACTTCCATT CTGCCATCATCACCATCAACATCACCACCATCAACATCACCACCACCATCACCACCACTTCCATT GTAG TTGA TRPM2-AS Ensembl:ENSG00000230061 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44419718..44419958 26863196 MeRIP-seq:(Medium) rs386819146 Functional Loss MNV dbSNP153 31..34 33 - - - Human_RBP_ID_207830,Human_RBP_ID_265180,Human_RBP_ID_2706339,Human_RBP_ID_24534176 62125 RMVar_ID_62125 Human_SNP_ID_696391014 m1A Human chr21 + 44434307 44434307 44434307 TGTGGCAGAGACGCTGGCAGGGATGGTGACGGAGACTGTGGCGAGGACTGTGGCAGGGACGCTGG TGTGGCAGAGACGCTGGCAGGGATGGTGACGGGGACTGTGGCGAGGACTGTGGCAGGGACGCTGG A G TRPM2 Ensembl:ENSG00000142185 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44434222..44434366 26863196 MeRIP-seq:(Medium) rs9979365 Functional Loss SNV dbSNP153 33..33 33 - - - 62126 RMVar_ID_62126 Human_SNP_ID_696391521 m1A Human chr21 + 44435683 44435663 44435683 CTCCACACCCATCCACGGGGACAGAGCCCCACACTCACCCCTCAGACTCACTTTCCACACCCATC CTCCACACCCATC____________________CTCACCCCTCAGACTCACTTTCCACACCCATC CCACGGGGACAGAGCCCCACA C TRPM2 Ensembl:ENSG00000142185 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44435675..44435749 26863196 MeRIP-seq:(Medium) rs1313914709 Functional Loss DEL dbSNP153 14..33 33 - - - 62127 RMVar_ID_62127 Human_SNP_ID_696393256 m1A Human chr21 - 44440903 44440903 44440903 CTCCCGCCTCCAGGGAGGCCAGGCACATACAGAGTTCAGCCTGTTCAGCTCCACGTCATTCTGGT CTCCCGCCTCCAGGGAGGCCAGGCACATACAGGGTTCAGCCTGTTCAGCTCCACGTCATTCTGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:44440895..44441122;chr21:44440887..44441112 26863196 MeRIP-seq:(Medium) rs1336552206 Functional Loss SNV dbSNP153 33..33 33 - - - 62128 RMVar_ID_62128 Human_SNP_ID_696393271 m1A Human chr21 + 44440955 44440935 44440955 CTGGAGGCGGGAGTGGGGAGGCAGGGACGGGTATGGGCGTGGCCTCCGGGGAGGGGGTTGGCAGG CTGGAGGCGGGAG____________________TGGGCGTGGCCTCCGGGGAGGGGGTTGGCAGG GTGGGGAGGCAGGGACGGGTA G TRPM2 Ensembl:ENSG00000142185 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44440910..44441116 26863196 MeRIP-seq:(Medium) rs1569126847 Functional Loss DEL dbSNP153 14..33 33 - - - 62129 RMVar_ID_62129 Human_SNP_ID_696393775 m1A Human chr21 + 44442535 44442535 44442535 GTGGCCAGGGACGGCATGAGCAGGAGGCGGGGACGTGGGGGCCTTCTGGTTTGGTGTCAACAGCT GTGGCCAGGGACGGCATGAGCAGGAGGCGGGGCCGTGGGGGCCTTCTGGTTTGGTGTCAACAGCT A C TRPM2 Ensembl:ENSG00000142185 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44442484..44442584 32194978 MeRIP-seq:(Medium) rs1433447250 Functional Loss SNV dbSNP153 33..33 33 - - - 62130 RMVar_ID_62130 Human_SNP_ID_696397470 m1A Human chr21 + 44456811 44456811 44456811 TGTGGCTGTCTTCTGCAGCTTGCGGGGCCTTCAGGAGGTCCCCGAGGACATCCCGGCCAACACCG TGTGGCTGTCTTCTGCAGCTTGCGGGGCCTTCGGGAGGTCCCCGAGGACATCCCGGCCAACACCG A G LRRC3 Ensembl:ENSG00000160233 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44455634..44457173 32194978 MeRIP-seq:(Medium) rs564773112 Functional Loss SNV dbSNP153 33..33 33 - - - 62131 RMVar_ID_62131 Human_SNP_ID_696398489 m1A Human chr21 + 44460256 44460256 44460256 GCCTGGAGCCCATGATGGACACTTGCGGAAGGAGGGGTGGCGGAGCACCCCTGAGATGACATCGC GCCTGGAGCCCATGATGGACACTTGCGGAAGGGGGGGTGGCGGAGCACCCCTGAGATGACATCGC A G LRRC3 Ensembl:ENSG00000160233 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44460206..44460406 32194978 MeRIP-seq:(Medium) rs974957341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572572,Human_RBP_ID_17981515 62132 RMVar_ID_62132 Human_SNP_ID_696405079 m1A Human chr21 + 44484860 44484815 44484860 GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGAGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG _________________________________GGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG CGGGGCGTCGGGGGCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGA C lnc-LRRC3-8,lnc-LRRC3-8:2 RNACentral:URS00008C11A4,RNACentral:URS00008B8EDC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44484852..44484985 26863196 MeRIP-seq:(Medium) rs780902625 Functional Loss DEL dbSNP153 1..33 33 - - - 62133 RMVar_ID_62133 Human_SNP_ID_696405151 m1A Human chr21 + 44484860 44484860 44484860 GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGAGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGCGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG A C lnc-LRRC3-8,lnc-LRRC3-8:2 RNACentral:URS00008C11A4,RNACentral:URS00008B8EDC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44484852..44484985 26863196 MeRIP-seq:(Medium) rs186875126 Functional Loss SNV dbSNP153 33..33 33 - - - 62134 RMVar_ID_62134 Human_SNP_ID_696405152 m1A Human chr21 + 44484860 44484860 44484860 GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGAGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGGGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG A G lnc-LRRC3-8,lnc-LRRC3-8:2 RNACentral:URS00008C11A4,RNACentral:URS00008B8EDC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44484852..44484985 26863196 MeRIP-seq:(Medium) rs186875126 Functional Loss SNV dbSNP153 33..33 33 - - - 62135 RMVar_ID_62135 Human_SNP_ID_696405153 m1A Human chr21 + 44484860 44484860 44484860 GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGAGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG GCGTGAGGGGCGTGCGGGGCGTGAGGGGCGTGTGGGGCGTGCGGGCGTGAGGGGCGTGAGGGGCG A T lnc-LRRC3-8,lnc-LRRC3-8:2 RNACentral:URS00008C11A4,RNACentral:URS00008B8EDC lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44484852..44484985 26863196 MeRIP-seq:(Medium) rs186875126 Functional Loss SNV dbSNP153 33..33 33 - - - 62136 RMVar_ID_62136 Human_SNP_ID_696411847 m1A Human chr21 - 44505567 44505561 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG______GAGGGGGTGATGTTTACTGGGTGCAGA CCCCCCT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911798 Functional Loss DEL dbSNP153 33..38 33 - - - 62137 RMVar_ID_62137 Human_SNP_ID_696411848 m1A Human chr21 - 44505567 44505562 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG_____GGAGGGGGTGATGTTTACTGGGTGCAGA CCCCCT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911799 Functional Loss DEL dbSNP153 33..37 33 - - - 62138 RMVar_ID_62138 Human_SNP_ID_696411849 m1A Human chr21 - 44505567 44505563 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG____GGGAGGGGGTGATGTTTACTGGGTGCAGA CCCCT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911801 Functional Loss DEL dbSNP153 33..36 33 - - - 62139 RMVar_ID_62139 Human_SNP_ID_696411850 m1A Human chr21 - 44505567 44505564 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG___GGGGAGGGGGTGATGTTTACTGGGTGCAGA CCCT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911802 Functional Loss DEL dbSNP153 33..35 33 - - - 62140 RMVar_ID_62140 Human_SNP_ID_696411851 m1A Human chr21 - 44505567 44505565 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG__GGGGGAGGGGGTGATGTTTACTGGGTGCAGA CCT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911803 Functional Loss DEL dbSNP153 33..34 33 - - - 62141 RMVar_ID_62141 Human_SNP_ID_696411852 m1A Human chr21 - 44505567 44505566 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGG_GGGGGGAGGGGGTGATGTTTACTGGGTGCAGA CT C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs1555911805 Functional Loss DEL dbSNP153 33..33 33 - - - 62142 RMVar_ID_62142 Human_SNP_ID_696411853 m1A Human chr21 - 44505567 44505567 44505567 TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGAGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA TGGGTGCCGGGGCTGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGTGATGTTTACTGGGTGCAGA T C TSPEAR Ensembl:ENSG00000175894 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44505551..44505681;chr21:44505551..44505684 26863196 MeRIP-seq:(Medium) rs200829812 Functional Loss SNV dbSNP153 33..33 33 - - - 62143 RMVar_ID_62143 Human_SNP_ID_696489401 m1A Human chr21 + 44770927 44770927 44770927 GGACTCCTCATGGGGCCCACAGGGAACCAGGAAGGACCCAGAAAGGGTGCCGGGCCCTTCCCCTG GGACTCCTCATGGGGCCCACAGGGAACCAGGAGGGACCCAGAAAGGGTGCCGGGCCCTTCCCCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44770878..44770978 32194978 MeRIP-seq:(Medium) rs2838678 Functional Loss SNV dbSNP153 33..33 33 - - - 62144 RMVar_ID_62144 Human_SNP_ID_696497179 m1A Human chr21 + 44801660 44801655 44801661 GCCCCAGCCCCGCCGGACGACGCGGGCCCGGGAGCAGGAACGCGGGACGCTGCTGACGGCCCGGG GCCCCAGCCCCGCCGGACGACGCGGGCC______CAGGAACGCGGGACGCTGCTGACGGCCCGGG CCGGGAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:44801658..44801800 26863196 MeRIP-seq:(Medium) rs1555964834 Functional Loss DEL dbSNP153 29..34 33 - - - 62145 RMVar_ID_62145 Human_SNP_ID_696497183 m1A Human chr21 + 44801660 44801660 44801660 GCCCCAGCCCCGCCGGACGACGCGGGCCCGGGAGCAGGAACGCGGGACGCTGCTGACGGCCCGGG GCCCCAGCCCCGCCGGACGACGCGGGCCCGGGGGCAGGAACGCGGGACGCTGCTGACGGCCCGGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:44801658..44801800 26863196 MeRIP-seq:(Medium) rs782386124 Functional Loss SNV dbSNP153 33..33 33 - - - 62146 RMVar_ID_62146 Human_SNP_ID_696497212 m1A Human chr21 - 44801714 44801714 44801714 GGCGGGGACCGCGCTCAAGAGGCTGATGGCCGAGTACAAACGTGAGTCTGGGGACCCGGGCCGTC GGCGGGGACCGCGCTCAAGAGGCTGATGGCCGTGTACAAACGTGAGTCTGGGGACCCGGGCCGTC T A UBE2G2 Ensembl:ENSG00000184787 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:44801695..44801781 26863410 MeRIP-seq:(Medium) rs3179387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928257,Human_RBP_ID_1606376,Human_RBP_ID_4676566,Human_RBP_ID_8544012,Human_RBP_ID_9123496,Human_RBP_ID_14345222,Human_RBP_ID_18423366,Human_RBP_ID_19007250,Human_RBP_ID_23009659,Human_RBP_ID_23930690,Human_RBP_ID_27029427 Human_Splice_Rec_2129711,Human_Splice_Rec_2129723,Human_Splice_Rec_2129729,Human_Splice_Rec_2129739,Human_Splice_Rec_2129751,Human_Splice_Rec_2129763,Human_Splice_Rec_2129773,Human_Splice_Rec_2129781,Human_Splice_Rec_2129787,Human_Splice_Rec_2129795,Human_Splice_Rec_2129803 62147 RMVar_ID_62147 Human_SNP_ID_696497242 m1A Human chr21 - 44801763 44801763 44801763 ACGCGCGCGGCTGAGGCGAGGTCGCTCGGCGCAGCTGTTGCGGGGCCATGGCGGGGACCGCGCTC ACGCGCGCGGCTGAGGCGAGGTCGCTCGGCGCCGCTGTTGCGGGGCCATGGCGGGGACCGCGCTC T G UBE2G2 Ensembl:ENSG00000184787 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44801652..44801825 26863196 MeRIP-seq:(Medium) rs782646823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245530,Human_RBP_ID_573767,Human_RBP_ID_4676567,Human_RBP_ID_7052835,Human_RBP_ID_14345233,Human_RBP_ID_18423367,Human_RBP_ID_19007250,Human_RBP_ID_23009659 Human_Splice_Rec_2129711,Human_Splice_Rec_2129723,Human_Splice_Rec_2129729,Human_Splice_Rec_2129739,Human_Splice_Rec_2129751,Human_Splice_Rec_2129763,Human_Splice_Rec_2129773,Human_Splice_Rec_2129781,Human_Splice_Rec_2129787,Human_Splice_Rec_2129795,Human_Splice_Rec_2129803 62148 RMVar_ID_62148 Human_SNP_ID_696498375 m1A Human chr21 - 44806275 44806275 44806275 GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCACCCCTCCCACCCCACTCCCTGCTCAGTACCTG GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCTCCCCTCCCACCCCACTCCCTGCTCAGTACCTG T A SUMO3 Ensembl:ENSG00000184900 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44806226..44806323 26863196 MeRIP-seq:(Medium) rs1247571913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573786,Human_RBP_ID_8206511,Human_RBP_ID_17397802,Human_RBP_ID_23930715 Human_miRNA_ID_466047,Human_miRNA_ID_1366529,Human_miRNA_ID_1561214,Human_miRNA_ID_2153995,Human_miRNA_ID_2801871,Human_miRNA_ID_3010003 RMVar_hsa_circ_91531,RMVar_hsa_circ_101684,RMVar_hsa_circ_122462,RMVar_hsa_circ_97155,RMVar_hsa_circ_212600,RMVar_hsa_circ_212602,RMVar_hsa_circ_212603,RMVar_hsa_circ_212601 62149 RMVar_ID_62149 Human_SNP_ID_696498376 m1A Human chr21 - 44806275 44806275 44806275 GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCACCCCTCCCACCCCACTCCCTGCTCAGTACCTG GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCGCCCCTCCCACCCCACTCCCTGCTCAGTACCTG T C SUMO3 Ensembl:ENSG00000184900 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44806226..44806323 26863196 MeRIP-seq:(Medium) rs1247571913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573786,Human_RBP_ID_8206511,Human_RBP_ID_17397802,Human_RBP_ID_23930715 Human_miRNA_ID_466047,Human_miRNA_ID_1366529,Human_miRNA_ID_1561214,Human_miRNA_ID_2153995,Human_miRNA_ID_2801871,Human_miRNA_ID_3010003 RMVar_hsa_circ_91531,RMVar_hsa_circ_101684,RMVar_hsa_circ_122462,RMVar_hsa_circ_97155,RMVar_hsa_circ_212600,RMVar_hsa_circ_212602,RMVar_hsa_circ_212603,RMVar_hsa_circ_212601 62150 RMVar_ID_62150 Human_SNP_ID_696498377 m1A Human chr21 - 44806275 44806275 44806275 GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCACCCCTCCCACCCCACTCCCTGCTCAGTACCTG GGGGTCTGAGGCCCAGGACCCACCCCCCTGCCCCCCCTCCCACCCCACTCCCTGCTCAGTACCTG T G SUMO3 Ensembl:ENSG00000184900 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44806226..44806323 26863196 MeRIP-seq:(Medium) rs1247571913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573786,Human_RBP_ID_8206511,Human_RBP_ID_17397802,Human_RBP_ID_23930715 Human_miRNA_ID_466047,Human_miRNA_ID_1366529,Human_miRNA_ID_1561214,Human_miRNA_ID_2153995,Human_miRNA_ID_2801871,Human_miRNA_ID_3010003 RMVar_hsa_circ_91531,RMVar_hsa_circ_101684,RMVar_hsa_circ_122462,RMVar_hsa_circ_97155,RMVar_hsa_circ_212600,RMVar_hsa_circ_212602,RMVar_hsa_circ_212603,RMVar_hsa_circ_212601 62151 RMVar_ID_62151 Human_SNP_ID_696499713 m1A Human chr21 + 44810958 44810956 44810958 ACATGCCCACACCCACACACATGCACACACCCACACATGCACACCCATGCACACACCCATGCACA ACATGCCCACACCCACACACATGCACACACC__CACATGCACACCCATGCACACACCCATGCACA CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44810956..44811113 26863196 MeRIP-seq:(Medium) rs1230697274 Functional Loss DEL dbSNP153 32..33 33 - - - 62152 RMVar_ID_62152 Human_SNP_ID_696500739 m1A Human chr21 - 44814092 44814092 44814092 GTCTCTGGTGTCTTCTGCAGGAGGGTGTGAAGACAGAGAATGACCACATCAACCTGAAGGTGGCC GTCTCTGGTGTCTTCTGCAGGAGGGTGTGAAGGCAGAGAATGACCACATCAACCTGAAGGTGGCC T C SUMO3 Ensembl:ENSG00000184900 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:44814026..44814125 26863196 MeRIP-seq:(Medium) rs774531863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928258,Human_RBP_ID_3961724,Human_RBP_ID_4679787,Human_RBP_ID_8942966,Human_RBP_ID_14345688,Human_RBP_ID_23930778,Human_RBP_ID_27302819 Human_Splice_Rec_2129808,Human_Splice_Rec_2129814,Human_Splice_Rec_2129820,Human_Splice_Rec_2129826,Human_Splice_Rec_2129832,Human_Splice_Rec_2129838 RMVar_hsa_circ_91531,RMVar_hsa_circ_101684,RMVar_hsa_circ_212602,RMVar_hsa_circ_212603,RMVar_hsa_circ_1839 62153 RMVar_ID_62153 Human_SNP_ID_696501596 m1A Human chr21 + 44817100 44817098 44817101 ATAGGGAGGGGTGGGCGCACACCAGGGACGCGATGATGGGGACGGGTGGGCGCACACCAGGTGGC ATAGGGAGGGGTGGGCGCACACCAGGGACGC___GATGGGGACGGGTGGGCGCACACCAGGTGGC CGAT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:44817095..44817224 26863196 MeRIP-seq:(Medium) rs1186689305 Functional Loss DEL dbSNP153 32..34 33 - - - 62154 RMVar_ID_62154 Human_SNP_ID_696501989 m1A Human chr21 - 44817935 44817927 44817936 TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGACCCCGCCTGCACGCGCGTCTATCGCGGGCGTC TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGC_________TGCACGCGCGTCTATCGCGGGCGTC AGGCGGGGTC A SUMO3 Ensembl:ENSG00000184900 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44817924..44818060 26863196 MeRIP-seq:(Medium) rs1456970916 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_780558,Human_RBP_ID_928514,Human_RBP_ID_19110402 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62155 RMVar_ID_62155 Human_SNP_ID_696501996 m1A Human chr21 - 44817935 44817933 44817935 TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGACCCCGCCTGCACGCGCGTCTATCGCGGGCGTC TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCG__CCCGCCTGCACGCGCGTCTATCGCGGGCGTC GGT G SUMO3 Ensembl:ENSG00000184900 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44817924..44818060 26863196 MeRIP-seq:(Medium) rs1384986698 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_780558,Human_RBP_ID_928514,Human_RBP_ID_19110402 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62156 RMVar_ID_62156 Human_SNP_ID_696501997 m1A Human chr21 - 44817935 44817934 44817935 TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGACCCCGCCTGCACGCGCGTCTATCGCGGGCGTC TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCG_CCCCGCCTGCACGCGCGTCTATCGCGGGCGTC GT G SUMO3 Ensembl:ENSG00000184900 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44817924..44818060 26863196 MeRIP-seq:(Medium) rs1300535340 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_780558,Human_RBP_ID_928514,Human_RBP_ID_19110402 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62157 RMVar_ID_62157 Human_SNP_ID_696501998 m1A Human chr21 - 44817935 44817935 44817935 TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGACCCCGCCTGCACGCGCGTCTATCGCGGGCGTC TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGGCCCCGCCTGCACGCGCGTCTATCGCGGGCGTC T C SUMO3 Ensembl:ENSG00000184900 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44817924..44818060 26863196 MeRIP-seq:(Medium) rs916475871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780558,Human_RBP_ID_928514,Human_RBP_ID_19110402 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62158 RMVar_ID_62158 Human_SNP_ID_696501999 m1A Human chr21 - 44817935 44817935 44817935 TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGACCCCGCCTGCACGCGCGTCTATCGCGGGCGTC TGTCCGAGGAGAAGCCCAAGGTAAGCGCGGCGCCCCCGCCTGCACGCGCGTCTATCGCGGGCGTC T G SUMO3 Ensembl:ENSG00000184900 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:44817924..44818060 26863196 MeRIP-seq:(Medium) rs916475871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780558,Human_RBP_ID_928514,Human_RBP_ID_19110402 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62159 RMVar_ID_62159 Human_SNP_ID_696502055 m1A Human chr21 + 44818023 44818023 44818023 GGCGGCGCGGGGGAAGCAGCGCGGAGCGGGCGAGTCACGCTCTCGGCCCCGCCGCTCTCCCGCCG GGCGGCGCGGGGGAAGCAGCGCGGAGCGGGCGGGTCACGCTCTCGGCCCCGCCGCTCTCCCGCCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:44813976..44818091;chr21:44813935..44818125;chr21:44817891..44818100 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1340175320 Functional Loss SNV dbSNP153 33..33 33 - - - 62160 RMVar_ID_62160 Human_SNP_ID_696502068 m1A Human chr21 - 44818048 44818048 44818048 TAAAGCGCGGCCCCGCGCACAGTTGCGGCGGGAGAGCGGCGGGGCCGAGAGCGTGACTCGCCCGC TAAAGCGCGGCCCCGCGCACAGTTGCGGCGGGGGAGCGGCGGGGCCGAGAGCGTGACTCGCCCGC T C SUMO3 Ensembl:ENSG00000184900 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:44817926..44818075 26863410 MeRIP-seq:(Medium) rs1046126361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679788 RMVar_hsa_circ_91531,RMVar_hsa_circ_212603 62161 RMVar_ID_62161 Human_SNP_ID_696512547 m1A Human chr21 - 44851500 44851500 44851500 GCAGCCCAGCCCAGCCGGGAGACCACGTGGCCATTGCGGTCTCCTGACCTTGGCCAGTGAACCTG GCAGCCCAGCCCAGCCGGGAGACCACGTGGCCGTTGCGGTCTCCTGACCTTGGCCAGTGAACCTG T C PTTG1IP Ensembl:ENSG00000183255 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44851451..44851600 32194978 MeRIP-seq:(Medium) rs1165364352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573878,Human_RBP_ID_4682962,Human_RBP_ID_14345997,Human_RBP_ID_17284782,Human_RBP_ID_17397811,Human_RBP_ID_17514067,Human_RBP_ID_26495734 Human_miRNA_ID_878712,Human_miRNA_ID_1348189,Human_miRNA_ID_1811397,Human_miRNA_ID_2676313,Human_miRNA_ID_2927066 RMVar_hsa_circ_113957,RMVar_hsa_circ_123018,RMVar_hsa_circ_122310,RMVar_hsa_circ_212605,RMVar_hsa_circ_88680,RMVar_hsa_circ_104447,RMVar_hsa_circ_212607,RMVar_hsa_circ_212609,RMVar_hsa_circ_80161,RMVar_hsa_circ_212608,RMVar_hsa_circ_212606,RMVar_hsa_circ_212604 62162 RMVar_ID_62162 Human_SNP_ID_696514044 m1A Human chr21 - 44856131 44856131 44856131 GTTACTTCGAGGGGATTCAGATCTGCAAGGCCATGGAAATCACATGGATACATCCTGAGTTTTCC GTTACTTCGAGGGGATTCAGATCTGCAAGGCCGTGGAAATCACATGGATACATCCTGAGTTTTCC T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44856130..44856375 26863196 MeRIP-seq:(Medium) rs1395408277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927547,Human_RBP_ID_5386923,Human_RBP_ID_14346126,Human_RBP_ID_22362221 RMVar_hsa_circ_113957,RMVar_hsa_circ_212605,RMVar_hsa_circ_88680,RMVar_hsa_circ_104447,RMVar_hsa_circ_212607,RMVar_hsa_circ_80161,RMVar_hsa_circ_212606,RMVar_hsa_circ_212611,RMVar_hsa_circ_122222,RMVar_hsa_circ_212604,RMVar_hsa_circ_288105,RMVar_hsa_circ_108705,RMVar_hsa_circ_212612,RMVar_hsa_circ_212610 62163 RMVar_ID_62163 Human_SNP_ID_696514100 m1A Human chr21 - 44856238 44856238 44856238 GAGGAGCCGGAAGCCGGACAGGAGTGAGGAGAAGGCCATGCGTGAGCGGGAGGAGAGGCGGATAC GAGGAGCCGGAAGCCGGACAGGAGTGAGGAGACGGCCATGCGTGAGCGGGAGGAGAGGCGGATAC T G PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44856137..44856375 26863196 MeRIP-seq:(Medium) rs759582287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64360,Human_RBP_ID_7052978,Human_RBP_ID_9348240,Human_RBP_ID_19007256,Human_RBP_ID_22453997,Human_RBP_ID_22768055,Human_RBP_ID_26344426 Human_Splice_Rec_2129855,Human_Splice_Rec_2129863,Human_Splice_Rec_2129871,Human_Splice_Rec_2129881 RMVar_hsa_circ_113957,RMVar_hsa_circ_212605,RMVar_hsa_circ_88680,RMVar_hsa_circ_104447,RMVar_hsa_circ_212607,RMVar_hsa_circ_80161,RMVar_hsa_circ_212606,RMVar_hsa_circ_212611,RMVar_hsa_circ_122222,RMVar_hsa_circ_212604,RMVar_hsa_circ_288105,RMVar_hsa_circ_108705,RMVar_hsa_circ_212612,RMVar_hsa_circ_212613,RMVar_hsa_circ_212610,RMVar_hsa_circ_359557 62164 RMVar_ID_62164 Human_SNP_ID_696514101 m1A Human chr21 - 44856241 44856239 44856242 GAAGAGGAGCCGGAAGCCGGACAGGAGTGAGGAGAAGGCCATGCGTGAGCGGGAGGAGAGGCGGA GAAGAGGAGCCGGAAGCCGGACAGGAGTGAG___AAGGCCATGCGTGAGCGGGAGGAGAGGCGGA TCTC T PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44856143..44856375 26863196 MeRIP-seq:(Medium) rs1284971855 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_64360,Human_RBP_ID_4676756,Human_RBP_ID_7052979,Human_RBP_ID_19007257,Human_RBP_ID_22453997,Human_RBP_ID_22768055,Human_RBP_ID_26344426 Human_Splice_Rec_2129855,Human_Splice_Rec_2129863,Human_Splice_Rec_2129871,Human_Splice_Rec_2129881 RMVar_hsa_circ_113957,RMVar_hsa_circ_212605,RMVar_hsa_circ_88680,RMVar_hsa_circ_104447,RMVar_hsa_circ_212607,RMVar_hsa_circ_80161,RMVar_hsa_circ_212606,RMVar_hsa_circ_212611,RMVar_hsa_circ_122222,RMVar_hsa_circ_212604,RMVar_hsa_circ_288105,RMVar_hsa_circ_108705,RMVar_hsa_circ_212612,RMVar_hsa_circ_212613,RMVar_hsa_circ_212610,RMVar_hsa_circ_359557 62165 RMVar_ID_62165 Human_SNP_ID_696515658 m1A Human chr21 + 44861240 44861240 44861240 CCGGTGGCAAGACGCTTGTAACTGGGTAGTCCAGACAAGCCTTGTTAGTGTTGCACCAAAGACAC CCGGTGGCAAGACGCTTGTAACTGGGTAGTCCCGACAAGCCTTGTTAGTGTTGCACCAAAGACAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:44861151..44861275 32194978 MeRIP-seq:(Medium) rs763445809 Functional Loss SNV dbSNP153 33..33 33 - - - 62166 RMVar_ID_62166 Human_SNP_ID_696515659 m1A Human chr21 + 44861240 44861240 44861240 CCGGTGGCAAGACGCTTGTAACTGGGTAGTCCAGACAAGCCTTGTTAGTGTTGCACCAAAGACAC CCGGTGGCAAGACGCTTGTAACTGGGTAGTCCGGACAAGCCTTGTTAGTGTTGCACCAAAGACAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:44861151..44861275 32194978 MeRIP-seq:(Medium) rs763445809 Functional Loss SNV dbSNP153 33..33 33 - - - 62167 RMVar_ID_62167 Human_SNP_ID_696516982 m1A Human chr21 + 44865442 44865442 44865442 GCACTCTTCACAGGTTTTGTTTGTGTTCTGAGAACAAGCTGCAGGAAAGAGGCAAGAGACAAGTC GCACTCTTCACAGGTTTTGTTTGTGTTCTGAGCACAAGCTGCAGGAAAGAGGCAAGAGACAAGTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44865426..44865450 32194978 MeRIP-seq:(Medium) rs13047375 Functional Loss SNV dbSNP153 33..33 33 - - - 62168 RMVar_ID_62168 Human_SNP_ID_696517225 m1A Human chr21 + 44866272 44866270 44866272 CCCCCAATCCCATAACACACACACACACACGCAGACTGCCTACTCCCCCAATCCCGTAACACACA CCCCCAATCCCATAACACACACACACACACG__GACTGCCTACTCCCCCAATCCCGTAACACACA GCA G lnc-FAM207A-6 RNACentral:URS00008B94ED lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:44866232..44866512 26863196 MeRIP-seq:(Medium) rs1340005558 Functional Loss DEL dbSNP153 32..33 33 - - - 62169 RMVar_ID_62169 Human_SNP_ID_696517244 m1A Human chr21 + 44866310 44866310 44866310 CCTACTCCCCCAATCCCGTAACACACACACAGACTGCCTACTCCCCCAATCCCATAACACACACA CCTACTCCCCCAATCCCGTAACACACACACAGTCTGCCTACTCCCCCAATCCCATAACACACACA A T lnc-FAM207A-6 RNACentral:URS00008B94ED lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44866298..44866369 26863196 MeRIP-seq:(Medium) rs1453132915 Functional Loss SNV dbSNP153 33..33 33 - - - 62170 RMVar_ID_62170 Human_SNP_ID_696517251 m1A Human chr21 + 44866333 44866332 44866334 CACACACAGACTGCCTACTCCCCCAATCCCATAACACACACACACACACACAGACTGCCTACTCC CACACACAGACTGCCTACTCCCCCAATCCCAT__CACACACACACACACACAGACTGCCTACTCC TAA T lnc-FAM207A-6 RNACentral:URS00008B94ED lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44866327..44866666 26863196 MeRIP-seq:(Medium) rs1491557966 Functional Loss DEL dbSNP153 33..34 33 - - - 62171 RMVar_ID_62171 Human_SNP_ID_696517261 m1A Human chr21 + 44866352 44866351 44866353 CCCCCAATCCCATAACACACACACACACACACAGACTGCCTACTCCAATCCCATAACACACACAC CCCCCAATCCCATAACACACACACACACACAC__ACTGCCTACTCCAATCCCATAACACACACAC CAG C lnc-FAM207A-6 RNACentral:URS00008B94ED lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:44866282..44866413 26863196 MeRIP-seq:(Medium) rs1173367074 Functional Loss DEL dbSNP153 33..34 33 - - - 62172 RMVar_ID_62172 Human_SNP_ID_696517293 m1A Human chr21 - 44866405 44866405 44866405 GTGTGTGTGTGTGTTATGGGATTGGAGTAGGCAGTCTCTGTGTGTGTGTGTGTGTGTGTGTGTTA GTGTGTGTGTGTGTTATGGGATTGGAGTAGGCTGTCTCTGTGTGTGTGTGTGTGTGTGTGTGTTA T A PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:44866149..44866682;chr21:44866126..44866677 26863196 MeRIP-seq:(Medium) rs1292467706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10010,Human_RBP_ID_5297655,Human_RBP_ID_5652922,Human_RBP_ID_17284702,Human_RBP_ID_23930933 RMVar_hsa_circ_80161,RMVar_hsa_circ_212604 62173 RMVar_ID_62173 Human_SNP_ID_696519444 m1A Human chr21 + 44873512 44873512 44873512 CCGCCCGCCCCGGCGCCCTCACCAGCTCCGGGAGGCTCCTGCGCGGCGGCCACCGGGATGAGCAG CCGCCCGCCCCGGCGCCCTCACCAGCTCCGGGTGGCTCCTGCGCGGCGGCCACCGGGATGAGCAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr21:44873501..44873625;chr21:44873501..44873675 32194978 MeRIP-seq:(Medium) rs1438277111 Functional Loss SNV dbSNP153 33..33 33 - - - 62174 RMVar_ID_62174 Human_SNP_ID_696539932 m1A Human chr21 + 44940095 44940095 44940095 GAAAGTGAGGGGGTTGCGCGCCCGAGTGCACCAGGCTGCCGTGAGGCCGAAAGGGGAGGCCGCCC GAAAGTGAGGGGGTTGCGCGCCCGAGTGCACCTGGCTGCCGTGAGGCCGAAAGGGGAGGCCGCCC A T FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44940044..44940261 26863196 MeRIP-seq:(Medium) rs777277247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573912,Human_RBP_ID_3667120,Human_RBP_ID_4679797,Human_RBP_ID_18782833 Human_Splice_Rec_2130341,Human_Splice_Rec_2130351,Human_Splice_Rec_2130359 RMVar_hsa_circ_212618,RMVar_hsa_circ_106102 62175 RMVar_ID_62175 Human_SNP_ID_696539939 m1A Human chr21 + 44940106 44940106 44940106 GGTTGCGCGCCCGAGTGCACCAGGCTGCCGTGAGGCCGAAAGGGGAGGCCGCCCCCGGCCCCGCG GGTTGCGCGCCCGAGTGCACCAGGCTGCCGTGGGGCCGAAAGGGGAGGCCGCCCCCGGCCCCGCG A G FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44940057..44940155 32194978 MeRIP-seq:(Medium) rs1357714253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573912,Human_RBP_ID_3667120,Human_RBP_ID_4679797 Human_Splice_Rec_2130341,Human_Splice_Rec_2130351,Human_Splice_Rec_2130359 RMVar_hsa_circ_212618,RMVar_hsa_circ_106102 62176 RMVar_ID_62176 Human_SNP_ID_696539967 m1A Human chr21 + 44940152 44940152 44940152 GGCCGCCCCCGGCCCCGCGCCCCCTGCCCCGGAGGCGACCCCTCCGCCGGCCTCGGCCGCGGGGA GGCCGCCCCCGGCCCCGCGCCCCCTGCCCCGGCGGCGACCCCTCCGCCGGCCTCGGCCGCGGGGA A C FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:44940051..44940225 26863410 MeRIP-seq:(Medium) rs926855539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679797,Human_RBP_ID_5323770,Human_RBP_ID_22454014 Human_Splice_Rec_2130341,Human_Splice_Rec_2130351,Human_Splice_Rec_2130359 Human_miRNA_ID_2153996,Human_miRNA_ID_2801872,Human_miRNA_ID_3010004 RMVar_hsa_circ_212618,RMVar_hsa_circ_106102 62177 RMVar_ID_62177 Human_SNP_ID_696539968 m1A Human chr21 + 44940152 44940152 44940152 GGCCGCCCCCGGCCCCGCGCCCCCTGCCCCGGAGGCGACCCCTCCGCCGGCCTCGGCCGCGGGGA GGCCGCCCCCGGCCCCGCGCCCCCTGCCCCGGTGGCGACCCCTCCGCCGGCCTCGGCCGCGGGGA A T FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:44940051..44940225 26863410 MeRIP-seq:(Medium) rs926855539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679797,Human_RBP_ID_5323770,Human_RBP_ID_22454014 Human_Splice_Rec_2130341,Human_Splice_Rec_2130351,Human_Splice_Rec_2130359 Human_miRNA_ID_2153996,Human_miRNA_ID_2801872,Human_miRNA_ID_3010004 RMVar_hsa_circ_212618,RMVar_hsa_circ_106102 62178 RMVar_ID_62178 Human_SNP_ID_696539985 m1A Human chr21 + 44940185 44940185 44940185 GGCGACCCCTCCGCCGGCCTCGGCCGCGGGGAAGGTGAGCTGGGGAGGCGCTGGCCGGGGGCTGC GGCGACCCCTCCGCCGGCCTCGGCCGCGGGGAGGGTGAGCTGGGGAGGCGCTGGCCGGGGGCTGC A G FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr21:44940051..44940233;chr21:44940115..44940202 26863196,26863410 MeRIP-seq:(Medium) rs1341534706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679797,Human_RBP_ID_5323770,Human_RBP_ID_19110905 Human_Splice_Rec_2130341,Human_Splice_Rec_2130351,Human_Splice_Rec_2130359 RMVar_hsa_circ_212618,RMVar_hsa_circ_106102 62179 RMVar_ID_62179 Human_SNP_ID_696540988 m1A Human chr21 + 44943771 44943771 44943771 CCTTGGTGCAGAAGCTGGAGCTGGACGTGAGGAGTGTCACTTCCGTCAGGAGAGGTGAGGCAGGC CCTTGGTGCAGAAGCTGGAGCTGGACGTGAGGCGTGTCACTTCCGTCAGGAGAGGTGAGGCAGGC A C FAM207A Ensembl:ENSG00000160256 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44943676..44943866 26863196 MeRIP-seq:(Medium) rs1483094673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7053104,Human_RBP_ID_9391548,Human_RBP_ID_14347444,Human_RBP_ID_19007261,Human_RBP_ID_24380924 Human_Splice_Rec_2130342,Human_Splice_Rec_2130343,Human_Splice_Rec_2130352,Human_Splice_Rec_2130353,Human_Splice_Rec_2130360,Human_Splice_Rec_2130361 Human_miRNA_ID_2709351 RMVar_hsa_circ_212619,RMVar_hsa_circ_322792,RMVar_hsa_circ_212618,RMVar_hsa_circ_106102,RMVar_hsa_circ_360188,RMVar_hsa_circ_373439,RMVar_hsa_circ_16662,RMVar_hsa_circ_84351,RMVar_hsa_circ_212620,RMVar_hsa_circ_212621 62180 RMVar_ID_62180 Human_SNP_ID_696542359 m1A Human chr21 + 44948324 44948324 44948324 GAGCATCGGGCGGTCCGGGGAGCTGGTCGTGGAGCATCGGGCGTCCGGGGAGCTGGTCGTGGAGC GAGCATCGGGCGGTCCGGGGAGCTGGTCGTGGCGCATCGGGCGTCCGGGGAGCTGGTCGTGGAGC A C FAM207A Ensembl:ENSG00000160256 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:44948039..44948622 26863196 MeRIP-seq:(Medium) rs1397814377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17397852,Human_RBP_ID_22723343,Human_RBP_ID_24425568 RMVar_hsa_circ_212619,RMVar_hsa_circ_322792,RMVar_hsa_circ_212618,RMVar_hsa_circ_106102,RMVar_hsa_circ_360188,RMVar_hsa_circ_373439,RMVar_hsa_circ_84351,RMVar_hsa_circ_212620,RMVar_hsa_circ_212621 62181 RMVar_ID_62181 Human_SNP_ID_696547800 m1A Human chr21 - 44967145 44967145 44967145 GGGCTTGGCGCCGGCTGCCAGCCTCGAGCCCCAGCAGCTCGGGCAGGGCATCCCTGAGAGGGTGC GGGCTTGGCGCCGGCTGCCAGCCTCGAGCCCCGGCAGCTCGGGCAGGGCATCCCTGAGAGGGTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44967095..44967223 26863196 MeRIP-seq:(Medium) rs1302811664 Functional Loss SNV dbSNP153 33..33 33 - - - 62182 RMVar_ID_62182 Human_SNP_ID_696551275 m1A Human chr21 + 44977170 44977170 44977170 TCCGTCCCTGAGCAGGCGCTGGTGCCCACAAGATAGTCTGCTGGCTGTGTTGGGAAGGAATTGTG TCCGTCCCTGAGCAGGCGCTGGTGCCCACAAGGTAGTCTGCTGGCTGTGTTGGGAAGGAATTGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44977119..44977614 26863196 MeRIP-seq:(Medium) rs569259680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1200341,Human_RBP_ID_4676881,Human_RBP_ID_8544134,Human_RBP_ID_14349142,Human_RBP_ID_23931153,Human_RBP_ID_26495747 62183 RMVar_ID_62183 Human_SNP_ID_696551374 m1A Human chr21 - 44977483 44977483 44977483 CCAGAGCAAGGCAGTGGGCTGCCTGGGTGTGGAGCAGCTGGGTAGGGTGAGGGCAACGGGTGGGG CCAGAGCAAGGCAGTGGGCTGCCTGGGTGTGGGGCAGCTGGGTAGGGTGAGGGCAACGGGTGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44977434..44977582 26863196 MeRIP-seq:(Medium) rs1438293934 Functional Loss SNV dbSNP153 33..33 33 - - - 62184 RMVar_ID_62184 Human_SNP_ID_696551559 m1A Human chr21 - 44978109 44978109 44978109 CAGGACACTGAACAGCAGGGACACAGGCTCCAACTTGCCTCGGCCACCCACTCGCCAGGCATCCT CAGGACACTGAACAGCAGGGACACAGGCTCCAGCTTGCCTCGGCCACCCACTCGCCAGGCATCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44978059..44978224 26863196 MeRIP-seq:(Medium) rs1206742602 Functional Loss SNV dbSNP153 33..33 33 - - - 62185 RMVar_ID_62185 Human_SNP_ID_696552038 m1A Human chr21 - 44978861 44978861 44978861 CTGCCGCCTCCCCACCGCGCTGTGCTCTGTGCATCCCGGACGCTGTTCCCAACACGCGCCCCACA CTGCCGCCTCCCCACCGCGCTGTGCTCTGTGCGTCCCGGACGCTGTTCCCAACACGCGCCCCACA T C lnc-ITGB2-3,lnc-ITGB2-3:2 RNACentral:URS00008C0AAA,RNACentral:URS00008C19D1 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44978811..44978894 26863196 MeRIP-seq:(Medium) rs1270155521 Functional Loss SNV dbSNP153 33..33 33 - - - 62186 RMVar_ID_62186 Human_SNP_ID_696552116 m1A Human chr21 + 44979120 44979120 44979120 CCGGGTGTGGTGGTGCGTGCCTGTAGTCAGCTACTGGGGAGGCTGAGGTGGGAGGATTGCTTGAG CCGGGTGTGGTGGTGCGTGCCTGTAGTCAGCTCCTGGGGAGGCTGAGGTGGGAGGATTGCTTGAG A C AP001505.1 Ensembl:ENSG00000276529 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44978880..44979130 32194978 MeRIP-seq:(Medium) rs984641356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573935,Human_RBP_ID_3666532,Human_RBP_ID_4682996,Human_RBP_ID_5119584,Human_RBP_ID_5653190,Human_RBP_ID_7053231,Human_RBP_ID_8115768,Human_RBP_ID_8235280,Human_RBP_ID_18168449,Human_RBP_ID_23931172,Human_RBP_ID_26495757 62187 RMVar_ID_62187 Human_SNP_ID_696552117 m1A Human chr21 + 44979120 44979120 44979120 CCGGGTGTGGTGGTGCGTGCCTGTAGTCAGCTACTGGGGAGGCTGAGGTGGGAGGATTGCTTGAG CCGGGTGTGGTGGTGCGTGCCTGTAGTCAGCTTCTGGGGAGGCTGAGGTGGGAGGATTGCTTGAG A T AP001505.1 Ensembl:ENSG00000276529 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44978880..44979130 32194978 MeRIP-seq:(Medium) rs984641356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573935,Human_RBP_ID_3666532,Human_RBP_ID_4682996,Human_RBP_ID_5119584,Human_RBP_ID_5653190,Human_RBP_ID_7053231,Human_RBP_ID_8115768,Human_RBP_ID_8235280,Human_RBP_ID_18168449,Human_RBP_ID_23931172,Human_RBP_ID_26495757 62188 RMVar_ID_62188 Human_SNP_ID_696552128 m1A Human chr21 - 44979174 44979174 44979174 CAGGTGGGAGTGCTGTGGCGCAATCTTGGCTCACTATAGCCACGGCCTCCTAGGCTCAAGCAATC CAGGTGGGAGTGCTGTGGCGCAATCTTGGCTCGCTATAGCCACGGCCTCCTAGGCTCAAGCAATC T C lnc-ITGB2-3,lnc-ITGB2-3:2 RNACentral:URS00008C0AAA,RNACentral:URS00008C19D1 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:44979124..44979202 26863196 MeRIP-seq:(Medium) rs945659474 Functional Loss SNV dbSNP153 33..33 33 - - - 62189 RMVar_ID_62189 Human_SNP_ID_696558525 m1A Human chr21 - 44997011 44997011 44997011 CCACCTTCCTCTGGGGGCACCCGCCTTCCTCCAGGGGCACCCACTATCCTCCCAGGATACCCATC CCACCTTCCTCTGGGGGCACCCGCCTTCCTCCTGGGGCACCCACTATCCTCCCAGGATACCCATC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:44996962..44997205 26863196 MeRIP-seq:(Medium) rs379754 Functional Loss SNV dbSNP153 33..33 33 - - - 62190 RMVar_ID_62190 Human_SNP_ID_696559378 m1A Human chr21 - 44999581 44999581 44999581 TGACTGAGAGCTCCAGCTCCGGAGAGGTGCCCAGTACCTGGTGAGCAGAGGGACCTGAAGGAGCA TGACTGAGAGCTCCAGCTCCGGAGAGGTGCCCGGTACCTGGTGAGCAGAGGGACCTGAAGGAGCA T C PICSAR Ensembl:ENSG00000275874 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:44999534..44999657 26863196 MeRIP-seq:(Medium) rs1233364117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2130384 62191 RMVar_ID_62191 Human_SNP_ID_696560398 m1A Human chr21 + 45002385 45002385 45002385 AGCTGGGGAGGGAGTTGGGTGAGGGGCTTGGGAGGGGGCTGGAGGCCACTCAAGTCAGGACGAAG AGCTGGGGAGGGAGTTGGGTGAGGGGCTTGGGGGGGGGCTGGAGGCCACTCAAGTCAGGACGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45002382..45002641 26863196 MeRIP-seq:(Medium) rs1183245219 Functional Loss SNV dbSNP153 33..33 33 - - - 62192 RMVar_ID_62192 Human_SNP_ID_696560401 m1A Human chr21 - 45002392 45002392 45002392 GCATCTTCTTCGTCCTGACTTGAGTGGCCTCCAGCCCCCTCCCAAGCCCCTCACCCAACTCCCTC GCATCTTCTTCGTCCTGACTTGAGTGGCCTCCGGCCCCCTCCCAAGCCCCTCACCCAACTCCCTC T C PICSAR Ensembl:ENSG00000275874 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45002381..45002629 26863196 MeRIP-seq:(Medium) rs189729943 Functional Loss SNV dbSNP153 33..33 33 - - - 62193 RMVar_ID_62193 Human_SNP_ID_696563868 m1A Human chr21 + 45014576 45014576 45014576 GGGGAGAGAGACAAGAGGGGCCGCCCCCGCCGAGCAGGGCCTGGTTGGGGGAGGAGCCACTCGGG GGGGAGAGAGACAAGAGGGGCCGCCCCCGCCGGGCAGGGCCTGGTTGGGGGAGGAGCCACTCGGG A G lnc-FAM207A-3 RNACentral:URS00009B9DD2 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45014526..45014699 26863196 MeRIP-seq:(Medium) rs550104764 Functional Loss SNV dbSNP153 33..33 33 - - - 62194 RMVar_ID_62194 Human_SNP_ID_696563876 m1A Human chr21 + 45014595 45014595 45014595 GCCGCCCCCGCCGAGCAGGGCCTGGTTGGGGGAGGAGCCACTCGGGGCCCTGGGCGGAGACAGAA GCCGCCCCCGCCGAGCAGGGCCTGGTTGGGGGGGGAGCCACTCGGGGCCCTGGGCGGAGACAGAA A G lnc-FAM207A-3 RNACentral:URS00009B9DD2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45014544..45014662 26863196 MeRIP-seq:(Medium) rs1037089274 Functional Loss SNV dbSNP153 33..33 33 - - - 62195 RMVar_ID_62195 Human_SNP_ID_696564879 m1A Human chr21 + 45018511 45018510 45018512 TCCTGGAGCAGGAGCGGCAGCGGGAAACGAAGACACGCGCTTCTTCCTACTGGGGGGATGGCTGG TCCTGGAGCAGGAGCGGCAGCGGGAAACGAAG__ACGCGCTTCTTCCTACTGGGGGGATGGCTGG GAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45018224..45018740 26863196 MeRIP-seq:(Medium) rs1366328838 Functional Loss DEL dbSNP153 33..34 33 - - - 62196 RMVar_ID_62196 Human_SNP_ID_696565238 m1A Human chr21 + 45019324 45019324 45019324 CATTCGTCACGCTCTATTATTGTAGGCAGCGCACCCCGGGGCTCGGTTCCCACACTGCGCCTGAG CATTCGTCACGCTCTATTATTGTAGGCAGCGCGCCCCGGGGCTCGGTTCCCACACTGCGCCTGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45019135..45019366 26863196 MeRIP-seq:(Medium) rs1038268621 Functional Loss SNV dbSNP153 33..33 33 - - - 62197 RMVar_ID_62197 Human_SNP_ID_696571428 m1A Human chr21 - 45042331 45042308 45042332 CACACACATTACACACACTACATACACACATCACGCATACACACCACACACACATATAAACCACA CACACACATTACACACACTACATACACACAT________________________ATAAACCACA TATGTGTGTGTGGTGTGTATGCGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45042235..45042657 26863196 MeRIP-seq:(Medium) rs1283124738 Functional Loss DEL dbSNP153 32..55 33 - - - 62198 RMVar_ID_62198 Human_SNP_ID_696571492 m1A Human chr21 - 45042398 45042395 45042399 ACACACACACCACACACATACACCACACACACACAACACACACTACACACACACCCCACACACAC ACACACACACCACACACATACACCACACACA____ACACACACTACACACACACCCCACACACAC TTGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45042347..45042598 26863196 MeRIP-seq:(Medium) rs759057927 Functional Loss DEL dbSNP153 32..35 33 - - - 62199 RMVar_ID_62199 Human_SNP_ID_696571493 m1A Human chr21 - 45042398 45042395 45042399 ACACACACACCACACACATACACCACACACACACAACACACACTACACACACACCCCACACACAC ACACACACACCACACACATACACCACACACA__CAACACACACTACACACACACCCCACACACAC TTGTG TTG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45042347..45042598 26863196 MeRIP-seq:(Medium) rs759057927 Functional Loss DEL dbSNP153 32..33 33 - - - 62200 RMVar_ID_62200 Human_SNP_ID_696571495 m1A Human chr21 - 45042398 45042396 45042399 ACACACACACCACACACATACACCACACACACACAACACACACTACACACACACCCCACACACAC ACACACACACCACACACATACACCACACACA___AACACACACTACACACACACCCCACACACAC TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45042347..45042598 26863196 MeRIP-seq:(Medium) rs1258992975 Functional Loss DEL dbSNP153 32..34 33 - - - 62201 RMVar_ID_62201 Human_SNP_ID_696571498 m1A Human chr21 - 45042398 45042398 45042398 ACACACACACCACACACATACACCACACACACACAACACACACTACACACACACCCCACACACAC ACACACACACCACACACATACACCACACACACTCAACACACACTACACACACACCCCACACACAC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45042347..45042598 26863196 MeRIP-seq:(Medium) rs1214022044 Functional Loss SNV dbSNP153 33..33 33 - - - 62202 RMVar_ID_62202 Human_SNP_ID_696571579 m1A Human chr21 - 45042487 45042486 45042488 CCCCCACACACTACACACACATTACACACTACATACACACATCACACACACACCACACACATACA CCCCCACACACTACACACACATTACACACTA__TACACACATCACACACACACCACACACATACA ATG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45042239..45042636 26863196 MeRIP-seq:(Medium) rs568651660 Functional Loss DEL dbSNP153 32..33 33 - - - 62203 RMVar_ID_62203 Human_SNP_ID_696578030 m1A Human chr21 + 45068942 45068942 45068942 ATGCTAGGCTGAGGCTCTTCGGGTCTGGAGCCAGGTTCCCTTCTTTCCTTTCTCCATTCTCTCTT ATGCTAGGCTGAGGCTCTTCGGGTCTGGAGCCGGGTTCCCTTCTTTCCTTTCTCCATTCTCTCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45068891..45069044 26863196 MeRIP-seq:(Medium) rs189033544 Functional Loss SNV dbSNP153 33..33 33 - - - 62204 RMVar_ID_62204 Human_SNP_ID_696579393 m1A Human chr21 - 45073898 45073897 45073899 CCCCCTCTCCCCGCCCGTCATCCTCACTGTAGACTCCGGGAGAACCAGGTCGCGGCCCAGGACCC CCCCCTCTCCCCGCCCGTCATCCTCACTGTA__CTCCGGGAGAACCAGGTCGCGGCCCAGGACCC GTC G SSR4P1 Ensembl:ENSG00000235374 Pseudogene exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:45073847..45074005 26863196 MeRIP-seq:(Medium) rs991073929 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14349631,Human_RBP_ID_17980871,Human_RBP_ID_18782881 62205 RMVar_ID_62205 Human_SNP_ID_696579395 m1A Human chr21 - 45073898 45073898 45073898 CCCCCTCTCCCCGCCCGTCATCCTCACTGTAGACTCCGGGAGAACCAGGTCGCGGCCCAGGACCC CCCCCTCTCCCCGCCCGTCATCCTCACTGTAGGCTCCGGGAGAACCAGGTCGCGGCCCAGGACCC T C SSR4P1 Ensembl:ENSG00000235374 Pseudogene exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:45073847..45074005 26863196 MeRIP-seq:(Medium) rs918133905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14349631,Human_RBP_ID_17980871,Human_RBP_ID_18782881 62206 RMVar_ID_62206 Human_SNP_ID_696579453 m1A Human chr21 + 45073967 45073967 45073967 CGGGACCCGCGTGTCCCAGGCAACTCCGGGAGAGGGAGAAGCAGGGGTGGCTCGGCGGGGGCTCG CGGGACCCGCGTGTCCCAGGCAACTCCGGGAGGGGGAGAAGCAGGGGTGGCTCGGCGGGGGCTCG A G ADARB1 Ensembl:ENSG00000197381 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45073866..45073966 26863410 MeRIP-seq:(Medium) rs1246615221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_207850,Human_RBP_ID_265198,Human_RBP_ID_928272,Human_RBP_ID_3665465,Human_RBP_ID_8115770,Human_RBP_ID_8942967,Human_RBP_ID_18168282,Human_RBP_ID_22723355,Human_RBP_ID_27840959 62207 RMVar_ID_62207 Human_SNP_ID_696579788 m1A Human chr21 + 45074415 45074415 45074415 CCAGCCCCAACGGCCCCGCGCCCGTCCGCCGCAGGTGGTCGTGAGGGAGGTGCCACAGCTCCGGC CCAGCCCCAACGGCCCCGCGCCCGTCCGCCGCGGGTGGTCGTGAGGGAGGTGCCACAGCTCCGGC A G ADARB1 Ensembl:ENSG00000197381 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:45074254..45074416 26863196 MeRIP-seq:(Medium) rs987613219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3665468,Human_RBP_ID_5240634,Human_RBP_ID_5323787,Human_RBP_ID_8115774,Human_RBP_ID_9332214,Human_RBP_ID_18496426,Human_RBP_ID_22371510,Human_RBP_ID_22723359,Human_RBP_ID_22744008,Human_RBP_ID_27840832 62208 RMVar_ID_62208 Human_SNP_ID_696580201 m1A Human chr21 - 45075080 45075075 45075080 TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGCAGCGCGGCGCATCCCACGCGGACTCGGCGCCCT TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGC_____GGCGCATCCCACGCGGACTCGGCGCCCT CGCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45075074..45075390 26863196 MeRIP-seq:(Medium) rs1354903429 Functional Loss DEL dbSNP153 33..37 33 - - - 62209 RMVar_ID_62209 Human_SNP_ID_696580203 m1A Human chr21 - 45075080 45075080 45075080 TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGCAGCGCGGCGCATCCCACGCGGACTCGGCGCCCT TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGCGGCGCGGCGCATCCCACGCGGACTCGGCGCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45075074..45075390 26863196 MeRIP-seq:(Medium) rs9977825 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7625,GWAS_ID_7626,GWAS_ID_7627,GWAS_ID_7628 62210 RMVar_ID_62210 Human_SNP_ID_696580204 m1A Human chr21 - 45075080 45075080 45075080 TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGCAGCGCGGCGCATCCCACGCGGACTCGGCGCCCT TCGTCCCGGCGCACCTGCCCTCCCCGCGGCGCCGCGCGGCGCATCCCACGCGGACTCGGCGCCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45075074..45075390 26863196 MeRIP-seq:(Medium) rs9977825 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7625,GWAS_ID_7626,GWAS_ID_7627,GWAS_ID_7628 62211 RMVar_ID_62211 Human_SNP_ID_696611802 m1A Human chr21 - 45201067 45201067 45201067 CATGGGAGGTGCCCACTCACAGCGTGCCATGAAGTGTGTTTGGCTGACACCCAAGGAACCTACAG CATGGGAGGTGCCCACTCACAGCGTGCCATGAGGTGTGTTTGGCTGACACCCAAGGAACCTACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45201062..45201162 32194978 MeRIP-seq:(Medium) rs1001668627 Functional Loss SNV dbSNP153 33..33 33 - - - 62212 RMVar_ID_62212 Human_SNP_ID_696612015 m1A Human chr21 + 45202019 45202019 45202019 GTGGCCAGAAGCTTGGGGACAGGTGCAGGGTGAGAGGTGACAGGGCTGGGGGATCTGGCCGGAGG GTGGCCAGAAGCTTGGGGACAGGTGCAGGGTGGGAGGTGACAGGGCTGGGGGATCTGGCCGGAGG A G ADARB1 Ensembl:ENSG00000197381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45202014..45202193 26863196 MeRIP-seq:(Medium) rs1397294705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14352376,Human_RBP_ID_21984437,Human_RBP_ID_22479663 RMVar_hsa_circ_297980,RMVar_hsa_circ_212639,RMVar_hsa_circ_31565,RMVar_hsa_circ_212626,RMVar_hsa_circ_330172,RMVar_hsa_circ_212635,RMVar_hsa_circ_296463,RMVar_hsa_circ_212636,RMVar_hsa_circ_373075,RMVar_hsa_circ_212638,RMVar_hsa_circ_275565,RMVar_hsa_circ_95611,RMVar_hsa_circ_212641,RMVar_hsa_circ_212642,RMVar_hsa_circ_212640,RMVar_hsa_circ_312830,RMVar_hsa_circ_212644 62213 RMVar_ID_62213 Human_SNP_ID_696628659 m1A Human chr21 - 45264970 45264970 45264970 GGCCTCATGAATCTCTCCGTTGCCCTCCGCGCAGCAGGAGGCTGCCTGTGTGTTTCCTCCTGGGA GGCCTCATGAATCTCTCCGTTGCCCTCCGCGCGGCAGGAGGCTGCCTGTGTGTTTCCTCCTGGGA T C POFUT2 Ensembl:ENSG00000186866 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45264920..45265468 32194978 MeRIP-seq:(Medium) rs925888257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26496069 Human_miRNA_ID_1094508 62214 RMVar_ID_62214 Human_SNP_ID_696633354 m1A Human chr21 - 45280690 45280690 45280690 AAGACGGGATCCGTGCAATTGAGACGAAACTCAGCGAGTGAGGGACGGGCAGCCTGGGGTGAGGT AAGACGGGATCCGTGCAATTGAGACGAAACTCGGCGAGTGAGGGACGGGCAGCCTGGGGTGAGGT T C POFUT2 Ensembl:ENSG00000186866 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45280607..45280855 26863196 MeRIP-seq:(Medium) rs1422997290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14353399 RMVar_hsa_circ_6597,RMVar_hsa_circ_39066,RMVar_hsa_circ_54466,RMVar_hsa_circ_13596,RMVar_hsa_circ_55348,RMVar_hsa_circ_359002,RMVar_hsa_circ_212646 62215 RMVar_ID_62215 Human_SNP_ID_696633355 m1A Human chr21 + 45280692 45280692 45280692 CTCACCCCAGGCTGCCCGTCCCTCACTCGCTGAGTTTCGTCTCAATTGCACGGATCCCGTCTTGG CTCACCCCAGGCTGCCCGTCCCTCACTCGCTGGGTTTCGTCTCAATTGCACGGATCCCGTCTTGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:45280674..45280807 26863196 MeRIP-seq:(Medium) rs542713058 Functional Loss SNV dbSNP153 33..33 33 - - - 62216 RMVar_ID_62216 Human_SNP_ID_696635908 m1A Human chr21 - 45288125 45288125 45288125 GCCCCTGCGTGGGCTGCGCCAGGGCGCCCGCGACAGCACCGCCGCGAACCACAGCCACGGCCTCC GCCCCTGCGTGGGCTGCGCCAGGGCGCCCGCGTCAGCACCGCCGCGAACCACAGCCACGGCCTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45288085..45289358 26863196 MeRIP-seq:(Medium) rs1418267317 Functional Loss SNV dbSNP153 33..33 33 - - - 62217 RMVar_ID_62217 Human_SNP_ID_696637369 m1A Human chr21 - 45292795 45292795 45292795 GGCCCAGGGCCTGCTCTCAGGGGTCGCTGGGGACAGGAGAGGCTCCGACAGGGGCCGCCCAGTGT GGCCCAGGGCCTGCTCTCAGGGGTCGCTGGGGGCAGGAGAGGCTCCGACAGGGGCCGCCCAGTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45292745..45292844 26863196 MeRIP-seq:(Medium) rs1267712193 Functional Loss SNV dbSNP153 33..33 33 - - - 62218 RMVar_ID_62218 Human_SNP_ID_696645149 m1A Human chr21 - 45320990 45320989 45320990 TCCCAGGGTTACATCTTAAGGGGCCTGGCAGCACCCGCCTGGGTCTCTGGGGATGCTCCCCCTCG TCCCAGGGTTACATCTTAAGGGGCCTGGCAGC_CCCGCCTGGGTCTCTGGGGATGCTCCCCCTCG GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45320958..45321112 26863196 MeRIP-seq:(Medium) rs1347191622 Functional Loss DEL dbSNP153 33..33 33 - - - 62219 RMVar_ID_62219 Human_SNP_ID_696645774 m1A Human chr21 - 45322744 45322744 45322744 CGCGAGGAAGAGGAGGGCGGGGCTGGGACAGGAGAACCCACGTGAGGAAGAGGAGGTGGGTGTTG CGCGAGGAAGAGGAGGGCGGGGCTGGGACAGGGGAACCCACGTGAGGAAGAGGAGGTGGGTGTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45322696..45322776 26863196 MeRIP-seq:(Medium) rs772511751 Functional Loss SNV dbSNP153 33..33 33 - - - 62220 RMVar_ID_62220 Human_SNP_ID_696647247 m1A Human chr21 - 45326818 45326818 45326818 GTGGCCATTGTCAGGGTGACTAAGAGATGACCAGCGTGGGTGGTATCGGGGGAAGCCAAGCCCGG GTGGCCATTGTCAGGGTGACTAAGAGATGACCGGCGTGGGTGGTATCGGGGGAAGCCAAGCCCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45326789..45326900 26863196 MeRIP-seq:(Medium) rs1569251371 Functional Loss SNV dbSNP153 33..33 33 - - - 62221 RMVar_ID_62221 Human_SNP_ID_696647263 m1A Human chr21 - 45326881 45326881 45326881 ATCAGGAAGGGCCAGTGGGGGCCTCCACACCCAGCCACAGAGCGTGGGACTGTCCTGTGAGCAGT ATCAGGAAGGGCCAGTGGGGGCCTCCACACCCGGCCACAGAGCGTGGGACTGTCCTGTGAGCAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45326831..45326982 26863196 MeRIP-seq:(Medium) rs549258240 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7629,GWAS_ID_7630 62222 RMVar_ID_62222 Human_SNP_ID_696648509 m1A Human chr21 + 45330751 45330751 45330751 CAGGACTCAGGGCCTCAGGGTGGAGGATGGTCAGGACTCAGGGCCTCAGGGTGGAGGCAGTCAGG CAGGACTCAGGGCCTCAGGGTGGAGGATGGTCGGGACTCAGGGCCTCAGGGTGGAGGCAGTCAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45330656..45330821 26863196 MeRIP-seq:(Medium) rs544061271 Functional Loss SNV dbSNP153 33..33 33 - - - 62223 RMVar_ID_62223 Human_SNP_ID_696659092 m1A Human chr21 - 45366604 45366603 45366604 ATACATGCCAATACTGCAACCTCGCATCTCAGAGGGGCCGAGTGCACACCACCACCCGCCCCGCC ATACATGCCAATACTGCAACCTCGCATCTCAG_GGGGCCGAGTGCACACCACCACCCGCCCCGCC CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45366554..45366712 32194978 MeRIP-seq:(Medium) rs1339358263 Functional Loss DEL dbSNP153 33..33 33 - - - 62224 RMVar_ID_62224 Human_SNP_ID_696683673 m1A Human chr21 + 45442853 45442835 45442853 CCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGAGGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT CCTGGTGTGGGCGGC__________________GGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT CGGTCCTGGTGTGGGCGGA C COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45442849..45443192 26863196 MeRIP-seq:(Medium) rs1261501195 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_5202103,Human_RBP_ID_8206060 62225 RMVar_ID_62225 Human_SNP_ID_696683681 m1A Human chr21 + 45442853 45442853 45442853 CCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGAGGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT CCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT A C COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45442849..45443192 26863196 MeRIP-seq:(Medium) rs867123420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5202103,Human_RBP_ID_8206060 62226 RMVar_ID_62226 Human_SNP_ID_696683682 m1A Human chr21 + 45442853 45442853 45442853 CCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGAGGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT CCTGGTGTGGGCGGCGGTCCTGGTGTGGGCGGTGGTCCTGGTGTGGGCGGTGGTGGTGCTGGTGT A T COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45442849..45443192 26863196 MeRIP-seq:(Medium) rs867123420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5202103,Human_RBP_ID_8206060 62227 RMVar_ID_62227 Human_SNP_ID_696692870 m1A Human chr21 + 45470890 45470890 45470890 CCTTGGAAGGTCAGAGAGCTGGAACAGGAGGGAGCTAGAGGGCCCTGGGTCTGGCCCTGGGCTGG CCTTGGAAGGTCAGAGAGCTGGAACAGGAGGGGGCTAGAGGGCCCTGGGTCTGGCCCTGGGCTGG A G COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45470886..45471165 26863196 MeRIP-seq:(Medium) rs1356816411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17145462,Human_RBP_ID_21984480 RMVar_hsa_circ_1151,RMVar_hsa_circ_347254,RMVar_hsa_circ_7945 62228 RMVar_ID_62228 Human_SNP_ID_696692888 m1A Human chr21 - 45470946 45470946 45470946 CCACCCACGCCCAGCAGCACACGGCCTGCTGCACGCCACCCACGCCCAGCAGGGCCCCAGCCCAG CCACCCACGCCCAGCAGCACACGGCCTGCTGCGCGCCACCCACGCCCAGCAGGGCCCCAGCCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45470944..45471210 26863196 MeRIP-seq:(Medium) rs555874994 Functional Loss SNV dbSNP153 33..33 33 - - - 62229 RMVar_ID_62229 Human_SNP_ID_696694029 m1A Human chr21 - 45474287 45474286 45474288 GACACACCACAGAGACACACCACACAAGACACAGAGACACACCACACAGACACAGACACACACAC GACACACCACAGAGACACACCACACAAGACA__GAGACACACCACACAGACACAGACACACACAC CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45474281..45474564 26863196 MeRIP-seq:(Medium) rs1219513000 Functional Loss DEL dbSNP153 32..33 33 - - - 62230 RMVar_ID_62230 Human_SNP_ID_696694048 m1A Human chr21 - 45474320 45474320 45474320 ACACACACACATCCACACACAACACACAAGACAGACACACCACAGAGACACACCACACAAGACAC ACACACACACATCCACACACAACACACAAGACGGACACACCACAGAGACACACCACACAAGACAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45474311..45474505 26863196 MeRIP-seq:(Medium) rs758890914 Functional Loss SNV dbSNP153 33..33 33 - - - 62231 RMVar_ID_62231 Human_SNP_ID_696694991 m1A Human chr21 + 45476423 45476423 45476423 TCACCACGCCACCCTTGGCTGGAGGCAGCAGCACGGAAGATTCCAGAAGTGAAGAAGTCGAGGAG TCACCACGCCACCCTTGGCTGGAGGCAGCAGCGCGGAAGATTCCAGAAGTGAAGAAGTCGAGGAG A G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:45476299..45476426 26863196 MeRIP-seq:(Medium) rs751212893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928288,Human_RBP_ID_3961334,Human_RBP_ID_22602186 Human_Splice_Rec_2130790,Human_Splice_Rec_2130791,Human_Splice_Rec_2130870,Human_Splice_Rec_2130871,Human_Splice_Rec_2130950,Human_Splice_Rec_2130951 RMVar_hsa_circ_1151,RMVar_hsa_circ_347254,RMVar_hsa_circ_7945,RMVar_hsa_circ_12706,RMVar_hsa_circ_55004,RMVar_hsa_circ_73405,RMVar_hsa_circ_16826 62232 RMVar_ID_62232 Human_SNP_ID_696695660 m1A Human chr21 - 45477833 45477833 45477833 GGACTCACTGGGCACGGGAGACCCGGGGGACCAGGTAGGCATGGGGATCCTGGGGGGCCTGCCCG GGACTCACTGGGCACGGGAGACCCGGGGGACCGGGTAGGCATGGGGATCCTGGGGGGCCTGCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45477784..45477892 26863196 MeRIP-seq:(Medium) rs779405324 Functional Loss SNV dbSNP153 33..33 33 - - - 62233 RMVar_ID_62233 Human_SNP_ID_696696750 m1A Human chr21 + 45480120 45480120 45480120 GAGAGAGGGCCCCCAGGACCCCAAGGGCCTCCAGGGCCCCCAGGACCCTCCTTCAGACACGACAA GAGAGAGGGCCCCCAGGACCCCAAGGGCCTCCGGGGCCCCCAGGACCCTCCTTCAGACACGACAA A G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45479970..45480125 26863196 MeRIP-seq:(Medium) rs1292887088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928299,Human_RBP_ID_9299332,Human_RBP_ID_18471353,Human_RBP_ID_19006799,Human_RBP_ID_22454030,Human_RBP_ID_24553681 Human_Splice_Rec_2130800,Human_Splice_Rec_2130801,Human_Splice_Rec_2130880,Human_Splice_Rec_2130881,Human_Splice_Rec_2130960,Human_Splice_Rec_2130961 RMVar_hsa_circ_347254,RMVar_hsa_circ_7945,RMVar_hsa_circ_73405,RMVar_hsa_circ_16826,RMVar_hsa_circ_367978 62234 RMVar_ID_62234 Human_SNP_ID_696699582 m1A Human chr21 - 45486986 45486986 45486986 GGGGGTCAGGTGTAGGCGGTACTCACAAATCCAGCGGGGAGTCCTGGTCCTGGGGGCCCAGGGGG GGGGGTCAGGTGTAGGCGGTACTCACAAATCCGGCGGGGAGTCCTGGTCCTGGGGGCCCAGGGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45486862..45489516 26863410 MeRIP-seq:(Medium) rs1439007572 Functional Loss SNV dbSNP153 33..33 33 - - - 62235 RMVar_ID_62235 Human_SNP_ID_696701468 m1A Human chr21 - 45491165 45491165 45491165 TTTCATCTCAACCGCTCTGGCCAGGACCCCAGAGTCCACCCAGCCCTGGAGGGGGTGCCCAGAGC TTTCATCTCAACCGCTCTGGCCAGGACCCCAGGGTCCACCCAGCCCTGGAGGGGGTGCCCAGAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45491162..45491357 26863196 MeRIP-seq:(Medium) rs781187328 Functional Loss SNV dbSNP153 33..33 33 - - - 62236 RMVar_ID_62236 Human_SNP_ID_696701471 m1A Human chr21 + 45491180 45491180 45491180 TCCAGGGCTGGGTGGACTCTGGGGTCCTGGCCAGAGCGGTTGAGATGAAATGCCGGACGCGTGGC TCCAGGGCTGGGTGGACTCTGGGGTCCTGGCCGGAGCGGTTGAGATGAAATGCCGGACGCGTGGC A G COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45491175..45491307 26863196 MeRIP-seq:(Medium) rs762821853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22673352 RMVar_hsa_circ_347254,RMVar_hsa_circ_8987,RMVar_hsa_circ_73405,RMVar_hsa_circ_16826,RMVar_hsa_circ_367978,RMVar_hsa_circ_48241 62237 RMVar_ID_62237 Human_SNP_ID_696703740 m1A Human chr21 + 45496567 45496567 45496567 AGGCCCTCCAGGGACTCCTGTTTACGACAGCAATGTAAGTCCCCAGGGCACCCACTGTCCTACAG AGGCCCTCCAGGGACTCCTGTTTACGACAGCAGTGTAAGTCCCCAGGGCACCCACTGTCCTACAG A G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45496542..45497679 26863410 MeRIP-seq:(Medium) rs762756737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2130838,Human_Splice_Rec_2130839,Human_Splice_Rec_2130918,Human_Splice_Rec_2130919,Human_Splice_Rec_2130998,Human_Splice_Rec_2130999,Human_Splice_Rec_2131042,Human_Splice_Rec_2131043,Human_Splice_Rec_2131076,Human_Splice_Rec_2131077 RMVar_hsa_circ_347254,RMVar_hsa_circ_73405,RMVar_hsa_circ_16826,RMVar_hsa_circ_48241 62238 RMVar_ID_62238 Human_SNP_ID_696705081 m1A Human chr21 + 45499699 45499699 45499699 TTAGAGGTTCCCGTGGTCTCAGCGCCCTGGGGAGTGGTGGTAGTTCTCACTATATTGGACGGTGA TTAGAGGTTCCCGTGGTCTCAGCGCCCTGGGGGGTGGTGGTAGTTCTCACTATATTGGACGGTGA A G COL18A1 Ensembl:ENSG00000182871 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:45499693..45500491 26863196 MeRIP-seq:(Medium) rs1319065268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5148861 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_48241 62239 RMVar_ID_62239 Human_SNP_ID_696705240 m1A Human chr21 - 45500134 45500134 45500134 CTACACACCCACATGCACACACTCCACACTCCACCCACACCCCCACACTGCACACACTCAGCACA CTACACACCCACATGCACACACTCCACACTCCCCCCACACCCCCACACTGCACACACTCAGCACA T G SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45500128..45500193 26863196 MeRIP-seq:(Medium) rs1022637370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_208225,Human_RBP_ID_24534441,Human_RBP_ID_26762004 62240 RMVar_ID_62240 Human_SNP_ID_696707466 m1A Human chr21 + 45504520 45504502 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCC__________________GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CGGCCCCCCCGGCCCCCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs201180574 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62241 RMVar_ID_62241 Human_SNP_ID_696707483 m1A Human chr21 + 45504520 45504509 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCC___________GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCCGGCCCCCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1345160374 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62242 RMVar_ID_62242 Human_SNP_ID_696707486 m1A Human chr21 + 45504520 45504510 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCC__________GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCGGCCCCCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1555874527 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62243 RMVar_ID_62243 Human_SNP_ID_696707493 m1A Human chr21 + 45504520 45504512 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCG________GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCCCCCCA G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs754870289 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62244 RMVar_ID_62244 Human_SNP_ID_696707496 m1A Human chr21 + 45504520 45504515 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCC_____GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCCCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs752450928 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62245 RMVar_ID_62245 Human_SNP_ID_696707497 m1A Human chr21 + 45504520 45504517 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCC___GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs757787509 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62246 RMVar_ID_62246 Human_SNP_ID_696707499 m1A Human chr21 + 45504520 45504518 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCC__GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs752020594 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62247 RMVar_ID_62247 Human_SNP_ID_696707504 m1A Human chr21 + 45504520 45504520 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCCGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT A C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28696990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62248 RMVar_ID_62248 Human_SNP_ID_696707505 m1A Human chr21 + 45504520 45504520 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCGGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT A G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28696990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62249 RMVar_ID_62249 Human_SNP_ID_696707506 m1A Human chr21 + 45504520 45504520 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCTGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT A T COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28696990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 62250 RMVar_ID_62250 Human_SNP_ID_696709912 m1A Human chr21 - 45509413 45509413 45509413 CGCGGTGGGGTGGGGGTGCTCCCGCCGCGGGTAGGGGTTGCTGTCGTGCAGCTGCACCACGGGGG CGCGGTGGGGTGGGGGTGCTCCCGCCGCGGGTGGGGGTTGCTGTCGTGCAGCTGCACCACGGGGG T C SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:45509371..45509528 26863196 MeRIP-seq:(Medium) rs1039474023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_207529,Human_RBP_ID_265247,Human_RBP_ID_5652975,Human_RBP_ID_8206150,Human_RBP_ID_8729477,Human_RBP_ID_23931672,Human_RBP_ID_26789234 62251 RMVar_ID_62251 Human_SNP_ID_696712516 m1A Human chr21 - 45515259 45515259 45515259 TGGCCCCACAGGAGTTGTGAGCCCTCTAGGGCAGGGTGGGAGCCGGGACCCTCAGGTGTAGCTGA TGGCCCCACAGGAGTTGTGAGCCCTCTAGGGCTGGGTGGGAGCCGGGACCCTCAGGTGTAGCTGA T A SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45515210..45515361 32194978 MeRIP-seq:(Medium) rs1486061461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679814,Human_RBP_ID_8235297,Human_RBP_ID_17981525,Human_RBP_ID_18168357,Human_RBP_ID_26496243 Human_miRNA_ID_76854,Human_miRNA_ID_80021,Human_miRNA_ID_462099,Human_miRNA_ID_928592,Human_miRNA_ID_2868958 RMVar_hsa_circ_212653,RMVar_hsa_circ_105956,RMVar_hsa_circ_114076,RMVar_hsa_circ_122079,RMVar_hsa_circ_212655,RMVar_hsa_circ_82513,RMVar_hsa_circ_212654,RMVar_hsa_circ_212652 62252 RMVar_ID_62252 Human_SNP_ID_696717855 m1A Human chr21 - 45531694 45531694 45531694 GCGCCCCAAGCGCAGCCTCTTCTTCAACCGCGACGACCGGGGGCGGTGCGAAACCTCGGCTTCGG GCGCCCCAAGCGCAGCCTCTTCTTCAACCGCGGCGACCGGGGGCGGTGCGAAACCTCGGCTTCGG T C SLC19A1 Ensembl:ENSG00000173638 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:45531533..45531855 26863196 MeRIP-seq:(Medium) rs1327888153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_208821,Human_RBP_ID_17701430,Human_RBP_ID_18783061,Human_RBP_ID_22767991 Human_miRNA_ID_2917569 RMVar_hsa_circ_212653,RMVar_hsa_circ_114076,RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_294117,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_376209,RMVar_hsa_circ_212656,RMVar_hsa_circ_338680,RMVar_hsa_circ_212658 62253 RMVar_ID_62253 Human_SNP_ID_696718055 m1A Human chr21 + 45532090 45532090 45532090 GCGTGTAGCGCAGGTAGTCGGTGAGCAGGAACACGGGCACCAGCACGGCCAGGTAGGAGTACGAC GCGTGTAGCGCAGGTAGTCGGTGAGCAGGAACCCGGGCACCAGCACGGCCAGGTAGGAGTACGAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45532040..45532131 26863196 MeRIP-seq:(Medium) rs1431775971 Functional Loss SNV dbSNP153 33..33 33 - - - 62254 RMVar_ID_62254 Human_SNP_ID_696719632 m1A Human chr21 - 45537425 45537424 45537425 CTTCTGGAATAGGCACGTGGGTGCTGGGTGCCAGGGCGGCCGCCTATGGGTGGGCGGGGAGCAGC CTTCTGGAATAGGCACGTGGGTGCTGGGTGCC_GGGCGGCCGCCTATGGGTGGGCGGGGAGCAGC CT C SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45537423..45537761 26863196 MeRIP-seq:(Medium) rs1182554764 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_265272,Human_RBP_ID_5323646,Human_RBP_ID_8116432,Human_RBP_ID_8206182,Human_RBP_ID_9432250,Human_RBP_ID_17670997,Human_RBP_ID_21984788,Human_RBP_ID_22723180,Human_RBP_ID_26789253 RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680 62255 RMVar_ID_62255 Human_SNP_ID_696719633 m1A Human chr21 - 45537425 45537425 45537425 CTTCTGGAATAGGCACGTGGGTGCTGGGTGCCAGGGCGGCCGCCTATGGGTGGGCGGGGAGCAGC CTTCTGGAATAGGCACGTGGGTGCTGGGTGCCGGGGCGGCCGCCTATGGGTGGGCGGGGAGCAGC T C SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45537423..45537761 26863196 MeRIP-seq:(Medium) rs1258276007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_265272,Human_RBP_ID_5323646,Human_RBP_ID_8116432,Human_RBP_ID_8206182,Human_RBP_ID_9432250,Human_RBP_ID_17670997,Human_RBP_ID_21984788,Human_RBP_ID_22723180,Human_RBP_ID_26789253 RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680 62256 RMVar_ID_62256 Human_SNP_ID_696719766 m1A Human chr21 - 45537669 45537669 45537669 CACGTGGGCGCCGGGATGCGGGGGCGGCCGCCAGTGGGTGGGCAGGGAGCAGCTTCTGGAATAGG CACGTGGGCGCCGGGATGCGGGGGCGGCCGCCTGTGGGTGGGCAGGGAGCAGCTTCTGGAATAGG T A SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45537640..45537724 26863196 MeRIP-seq:(Medium) rs1405962435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_208335,Human_RBP_ID_265085,Human_RBP_ID_833009,Human_RBP_ID_927625,Human_RBP_ID_3666227,Human_RBP_ID_5240687,Human_RBP_ID_5323648,Human_RBP_ID_5386359,Human_RBP_ID_5652986,Human_RBP_ID_8115937,Human_RBP_ID_8206186,Human_RBP_ID_8943115,Human_RBP_ID_9332511,Human_RBP_ID_9431962,Human_RBP_ID_17397860,Human_RBP_ID_18496880,Human_RBP_ID_18952135,Human_RBP_ID_19110940,Human_RBP_ID_22723181,Human_RBP_ID_22744124,Human_RBP_ID_24380620 RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680 62257 RMVar_ID_62257 Human_SNP_ID_696719945 m1A Human chr21 - 45537962 45537962 45537962 TCGTCCCCTCCGGAGCTGCACGTGGCCTGAGCAGGATGGTGCCCTCCAGCCCAGCGGTGGAGAAG TCGTCCCCTCCGGAGCTGCACGTGGCCTGAGCGGGATGGTGCCCTCCAGCCCAGCGGTGGAGAAG T C SLC19A1 Ensembl:ENSG00000173638 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45537801..45538047 26863410 MeRIP-seq:(Medium) rs1051340641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1606632,Human_RBP_ID_4677782,Human_RBP_ID_8942999,Human_RBP_ID_18193928,Human_RBP_ID_22264709,Human_RBP_ID_22454059,Human_RBP_ID_26495832,Human_RBP_ID_26821877,Human_RBP_ID_27303314 Human_Splice_Rec_2131122,Human_Splice_Rec_2131134,Human_Splice_Rec_2131148,Human_Splice_Rec_2131156,Human_Splice_Rec_2131172,Human_Splice_Rec_2131174,Human_Splice_Rec_2131178 RMVar_hsa_circ_100596,RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680,RMVar_hsa_circ_212662,RMVar_hsa_circ_90442,RMVar_hsa_circ_212661 62258 RMVar_ID_62258 Human_SNP_ID_696719946 m1A Human chr21 - 45537962 45537962 45537962 TCGTCCCCTCCGGAGCTGCACGTGGCCTGAGCAGGATGGTGCCCTCCAGCCCAGCGGTGGAGAAG TCGTCCCCTCCGGAGCTGCACGTGGCCTGAGCCGGATGGTGCCCTCCAGCCCAGCGGTGGAGAAG T G SLC19A1 Ensembl:ENSG00000173638 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45537801..45538047 26863410 MeRIP-seq:(Medium) rs1051340641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1606632,Human_RBP_ID_4677782,Human_RBP_ID_8942999,Human_RBP_ID_18193928,Human_RBP_ID_22264709,Human_RBP_ID_22454059,Human_RBP_ID_26495832,Human_RBP_ID_26821877,Human_RBP_ID_27303314 Human_Splice_Rec_2131122,Human_Splice_Rec_2131134,Human_Splice_Rec_2131148,Human_Splice_Rec_2131156,Human_Splice_Rec_2131172,Human_Splice_Rec_2131174,Human_Splice_Rec_2131178 RMVar_hsa_circ_100596,RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680,RMVar_hsa_circ_212662,RMVar_hsa_circ_90442,RMVar_hsa_circ_212661 62259 RMVar_ID_62259 Human_SNP_ID_696719979 m1A Human chr21 - 45538006 45538006 45538006 AAGGTGCCCTGACTCCACCCCTCCTTCCAGGCACAGCGTCACCTTCGTCCCCTCCGGAGCTGCAC AAGGTGCCCTGACTCCACCCCTCCTTCCAGGCCCAGCGTCACCTTCGTCCCCTCCGGAGCTGCAC T G SLC19A1 Ensembl:ENSG00000173638 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:45537914..45538034 26863196 MeRIP-seq:(Medium) rs1415495298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1068739,Human_RBP_ID_4679986 Human_Splice_Rec_2131122,Human_Splice_Rec_2131134,Human_Splice_Rec_2131148,Human_Splice_Rec_2131156,Human_Splice_Rec_2131172,Human_Splice_Rec_2131174,Human_Splice_Rec_2131178 RMVar_hsa_circ_100596,RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_338680,RMVar_hsa_circ_212662,RMVar_hsa_circ_90442,RMVar_hsa_circ_212661 62260 RMVar_ID_62260 Human_SNP_ID_696721229 m1A Human chr21 + 45542316 45542316 45542316 CCCGCGCCCCGCACTCACCCCAGGGCCCCGAGACACCCCGCAGCCCCCGACACGCGGCCCCGTGG CCCGCGCCCCGCACTCACCCCAGGGCCCCGAGCCACCCCGCAGCCCCCGACACGCGGCCCCGTGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45542309..45542394 26863410 MeRIP-seq:(Medium) rs1406299603 Functional Loss SNV dbSNP153 33..33 33 - - - 62261 RMVar_ID_62261 Human_SNP_ID_696721272 m1A Human chr21 + 45542405 45542405 45542405 ACTCGGCGGGGCGGCTGCCCTGGGGCTCCCGGACCCGGCCCCGCGCACGCGGACTCCGGGACTAC ACTCGGCGGGGCGGCTGCCCTGGGGCTCCCGGCCCCGGCCCCGCGCACGCGGACTCCGGGACTAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:45542235..45542413;chr21:45542236..45542406 26863196 MeRIP-seq:(Medium) rs1160908574 Functional Loss SNV dbSNP153 33..33 33 - - - 62262 RMVar_ID_62262 Human_SNP_ID_696724313 m1A Human chr21 - 45553187 45553187 45553187 GAAGGACCAGTAGAGCTTGCAGGGCAGGACCCAGCCCCAGCCTCTGCTTACAAAACTGCACCCAC GAAGGACCAGTAGAGCTTGCAGGGCAGGACCCGGCCCCAGCCTCTGCTTACAAAACTGCACCCAC T C SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45553136..45553223 26863196 MeRIP-seq:(Medium) rs1308997105 Functional Loss SNV dbSNP153 33..33 33 - - - 62263 RMVar_ID_62263 Human_SNP_ID_696726409 m1A Human chr21 - 45556447 45556447 45556447 TTACAGATTTCAAGCTTCTCTTGAAAAGTTGGAAGCACCAAACACCCAAGCCCGGGCGCTGGTGG TTACAGATTTCAAGCTTCTCTTGAAAAGTTGGGAGCACCAAACACCCAAGCCCGGGCGCTGGTGG T C SLC19A1 Ensembl:ENSG00000173638 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45556348..45556465 32194978 MeRIP-seq:(Medium) rs953662277 Functional Loss SNV dbSNP153 33..33 33 - - - 62264 RMVar_ID_62264 Human_SNP_ID_696751210 m1A Human chr21 + 45643805 45643805 45643805 TCCGCCGCCGCCTCCTCACCCGCCTCGCCCCGACCCCGCCCGGGCCTCCCGGCCTCTCCCCGCCG TCCGCCGCCGCCTCCTCACCCGCCTCGCCCCGCCCCCGCCCGGGCCTCCCGGCCTCTCCCCGCCG A C PCBP3 Ensembl:ENSG00000183570 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45643716..45668898 26863410 MeRIP-seq:(Medium) rs919681010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2131199,Human_Splice_Rec_2131205,Human_Splice_Rec_2131235 62265 RMVar_ID_62265 Human_SNP_ID_696823069 m1A Human chr21 + 45924270 45924270 45924270 ACAGTCGCGTGGATAGAAACAGCACACGTAAGATCGGGTGTGCGTGAGGAGATGCGAACACCGGG ACAGTCGCGTGGATAGAAACAGCACACGTAAGGTCGGGTGTGCGTGAGGAGATGCGAACACCGGG A G PCBP3 Ensembl:ENSG00000183570 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:45924162..45924306 26863196 MeRIP-seq:(Medium) rs1215919117 Functional Loss SNV dbSNP153 33..33 33 - - - 62266 RMVar_ID_62266 Human_SNP_ID_696840090 m1A Human chr21 - 45981826 45981825 45981827 GCCCTCATGTCTGGGGCCTGCGGTCACCACACAGCGCGGCCAGGGCAGAGTGGGCCGCCGCCGCC GCCCTCATGTCTGGGGCCTGCGGTCACCACA__GCGCGGCCAGGGCAGAGTGGGCCGCCGCCGCC CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:45981778..45981862 26863196 MeRIP-seq:(Medium) rs748707382 Functional Loss DEL dbSNP153 32..33 33 - - - 62267 RMVar_ID_62267 Human_SNP_ID_696847585 m1A Human chr21 - 46000344 46000344 46000344 GATACTCACAGCACATTTTCATGATGATGTCCAAAATCTCGCATTCCTGGGGAGGGAGAGACGAG GATACTCACAGCACATTTTCATGATGATGTCCCAAATCTCGCATTCCTGGGGAGGGAGAGACGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:45999651..46000799 32194978 MeRIP-seq:(Medium) rs201365474 Functional Loss SNV dbSNP153 33..33 33 - - - 62268 RMVar_ID_62268 Human_SNP_ID_696849426 m1A Human chr21 - 46004301 46004260 46004302 CCAGCTCAGGGCTGAGCCCCAGAGGGCCCTGCACAGGTGACGCCAGCTCAGGGCTGAGCCTCAGA CCAGCTCAGGGCTGAGCCCCAGAGGGCCCTG__________________________________ ACAGGGCCCTCTGAGGCTCAGCCCTGAGCTGGCGTCACCTGTG A HSALNG0133691 RNACentral:URS0000EAE1DB lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:46004201..46004500 26863410 MeRIP-seq:(Medium) rs1245879613 Functional Loss DEL dbSNP153 32..65 33 - - - 62269 RMVar_ID_62269 Human_SNP_ID_696849451 m1A Human chr21 - 46004301 46004301 46004301 CCAGCTCAGGGCTGAGCCCCAGAGGGCCCTGCACAGGTGACGCCAGCTCAGGGCTGAGCCTCAGA CCAGCTCAGGGCTGAGCCCCAGAGGGCCCTGCGCAGGTGACGCCAGCTCAGGGCTGAGCCTCAGA T C HSALNG0133691 RNACentral:URS0000EAE1DB lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:46004201..46004500 26863410 MeRIP-seq:(Medium) rs533201643 Functional Loss SNV dbSNP153 33..33 33 - - - 62270 RMVar_ID_62270 Human_SNP_ID_696849489 m1A Human chr21 - 46004387 46004387 46004387 TGCCTAGGGAAGGAGCTGCGCAGGCAGGAGGGAGGGCGGGCAGGAGGGCAGGGCAGGAGAGCCCG TGCCTAGGGAAGGAGCTGCGCAGGCAGGAGGGCGGGCGGGCAGGAGGGCAGGGCAGGAGAGCCCG T G HSALNG0133691 RNACentral:URS0000EAE1DB lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46004339..46004431 26863196 MeRIP-seq:(Medium) rs1409662119 Functional Loss SNV dbSNP153 33..33 33 - - - 62271 RMVar_ID_62271 Human_SNP_ID_696882899 m1A Human chr21 + 46116044 46116044 46116044 GACCCGGGCATCGAAGGCCCCATTGGATTCCCAGGACCCAAGGTGAGTGACCTCGGCCAGGGGCT GACCCGGGCATCGAAGGCCCCATTGGATTCCCGGGACCCAAGGTGAGTGACCTCGGCCAGGGGCT A G COL6A2 Ensembl:ENSG00000142173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46114001..46117475 32194978 MeRIP-seq:(Medium) rs1008037230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2131646,Human_Splice_Rec_2131647,Human_Splice_Rec_2131700,Human_Splice_Rec_2131701,Human_Splice_Rec_2131756,Human_Splice_Rec_2131757,Human_Splice_Rec_2131808,Human_Splice_Rec_2131809,Human_Splice_Rec_2131856,Human_Splice_Rec_2131857 Human_miRNA_ID_2041763,Human_miRNA_ID_3020741 RMVar_hsa_circ_11956,RMVar_hsa_circ_95548,RMVar_hsa_circ_127076,RMVar_hsa_circ_79099,RMVar_hsa_circ_212691,RMVar_hsa_circ_212690,RMVar_hsa_circ_56765,RMVar_hsa_circ_43545,RMVar_hsa_circ_212692,RMVar_hsa_circ_352705 62272 RMVar_ID_62272 Human_SNP_ID_696891671 m1A Human chr21 + 46132500 46132500 46132500 CCGCGCCGCCGTGTTCCACGAGAAGGACTATGACAGCCTGGCGCAACCCGGCTTCTTCGACCGCT CCGCGCCGCCGTGTTCCACGAGAAGGACTATGGCAGCCTGGCGCAACCCGGCTTCTTCGACCGCT A G COL6A2 Ensembl:ENSG00000142173 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:46132451..46132850 32194978 MeRIP-seq:(Medium) rs1174824223 Functional Loss SNV dbSNP153 33..33 33 - - - 62273 RMVar_ID_62273 Human_SNP_ID_696898188 m1A Human chr21 - 46144268 46144264 46144269 ATAGAAATAAAGACACAAGACAAAGAGAAGAAAAGACAGCTGGGCCCGGGGGACCACTACCACTA ATAGAAATAAAGACACAAGACAAAGAGAAGA_____CAGCTGGGCCCGGGGGACCACTACCACTA GTCTTT G FTCD Ensembl:ENSG00000160282 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:46144265..46144368 26863196 MeRIP-seq:(Medium) rs1276740847 Functional Loss DEL dbSNP153 32..36 33 - - - 62274 RMVar_ID_62274 Human_SNP_ID_696898850 m1A Human chr21 + 46145418 46145418 46145418 CCCGGGGAGCCCTGCTGTGGCCGCCACTCACCAGGTAGGCGGTGAAGGCCTCGGCGTCGGCATCC CCCGGGGAGCCCTGCTGTGGCCGCCACTCACCGGGTAGGCGGTGAAGGCCTCGGCGTCGGCATCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:46145417..46145556 26863196 MeRIP-seq:(Medium) rs1311683537 Functional Loss SNV dbSNP153 33..33 33 - - - 62275 RMVar_ID_62275 Human_SNP_ID_696899208 m1A Human chr21 + 46146001 46146001 46146001 GCGGGTCTGGCCGGGGTTGGTGGGGGGAGCGCAGTCCTCCCGGGGCGGCCCCAGGCCCCACGCCC GCGGGTCTGGCCGGGGTTGGTGGGGGGAGCGCCGTCCTCCCGGGGCGGCCCCAGGCCCCACGCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:46145950..46146075 26863196 MeRIP-seq:(Medium) rs1430017760 Functional Loss SNV dbSNP153 33..33 33 - - - 62276 RMVar_ID_62276 Human_SNP_ID_696904377 m1A Human chr21 + 46161279 46161279 46161279 AGCGGGGCCTTCTCTGGCCTCGCGCGCGGGGGACGCGGCCCTTTCCCCTCCGGGGGGACGCGCAG AGCGGGGCCTTCTCTGGCCTCGCGCGCGGGGGGCGCGGCCCTTTCCCCTCCGGGGGGACGCGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46161231..46161316 26863196 MeRIP-seq:(Medium) rs539607226 Functional Loss SNV dbSNP153 33..33 33 - - - 62277 RMVar_ID_62277 Human_SNP_ID_696904384 m1A Human chr21 - 46161295 46161295 46161295 GGGGCCGCGGTGCCTCCTGCGCGTCCCCCCGGAGGGGAAAGGGCCGCGTCCCCCGCGCGCGAGGC GGGGCCGCGGTGCCTCCTGCGCGTCCCCCCGGGGGGGAAAGGGCCGCGTCCCCCGCGCGCGAGGC T C SPATC1L Ensembl:ENSG00000160284 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46161197..46161297 32194978 MeRIP-seq:(Medium) rs1215567241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3666318 62278 RMVar_ID_62278 Human_SNP_ID_696904478 m1A Human chr21 - 46161431 46161431 46161431 CAAGTTCCTGGGCGACTCGCTGCTGCTGCTCAACTGCCTGTGCGAGCTCTCCAAGGAGGACGGCA CAAGTTCCTGGGCGACTCGCTGCTGCTGCTCAGCTGCCTGTGCGAGCTCTCCAAGGAGGACGGCA T C SPATC1L Ensembl:ENSG00000160284 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46161345..46161495 26863196 MeRIP-seq:(Medium) rs761070479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18193894,Human_RBP_ID_22453923,Human_RBP_ID_26821879 RMVar_hsa_circ_212703 62279 RMVar_ID_62279 Human_SNP_ID_696904892 m1A Human chr21 - 46162040 46162038 46162041 CCCAGAGATCCAGAGCTTCGCGGGCGCCGAGAAGGACGCGCGCGTGGTGGGCGAGATCGCCTTCC CCCAGAGATCCAGAGCTTCGCGGGCGCCGAG___GACGCGCGCGTGGTGGGCGAGATCGCCTTCC CCTT C SPATC1L Ensembl:ENSG00000160284 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:46161952..46162053 26863410 MeRIP-seq:(Medium) rs775298796 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_26821884 Human_Splice_Rec_2132054,Human_Splice_Rec_2132062 RMVar_hsa_circ_212703 62280 RMVar_ID_62280 Human_SNP_ID_696906627 m1A Human chr21 - 46168531 46168529 46168531 TCCAGCGAGGACGACACCTCCCCGGGCTGTGCAGCCCCCTCCCAGGCACCCTTCAAGGCCTTCCT TCCAGCGAGGACGACACCTCCCCGGGCTGTGC__CCCCCTCCCAGGCACCCTTCAAGGCCTTCCT GCT G SPATC1L Ensembl:ENSG00000160284 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46168480..46168670 26863196 MeRIP-seq:(Medium) rs749935979 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18193930,Human_RBP_ID_22453924 62281 RMVar_ID_62281 Human_SNP_ID_696906645 m1A Human chr21 - 46168553 46168553 46168553 GCTGTGCTCACATGCCCCCCTGTCCAGCGAGGACGACACCTCCCCGGGCTGTGCAGCCCCCTCCC GCTGTGCTCACATGCCCCCCTGTCCAGCGAGGGCGACACCTCCCCGGGCTGTGCAGCCCCCTCCC T C SPATC1L Ensembl:ENSG00000160284 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46168503..46168629 26863196 MeRIP-seq:(Medium) rs1010608695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22453924 62282 RMVar_ID_62282 Human_SNP_ID_696911124 m1A Human chr21 + 46184304 46184304 46184304 GAGCAGGCGTCTGTCCTCAGTCAGTGCGACCGACTTGAAACCCACCCTGACTCCCTGCTTCAATT GAGCAGGCGTCTGTCCTCAGTCAGTGCGACCGGCTTGAAACCCACCCTGACTCCCTGCTTCAATT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46184300..46184380 26863196 MeRIP-seq:(Medium) rs1260660815 Functional Loss SNV dbSNP153 33..33 33 - - - 62283 RMVar_ID_62283 Human_SNP_ID_696911126 m1A Human chr21 - 46184307 46184307 46184307 AGTAATTGAAGCAGGGAGTCAGGGTGGGTTTCAAGTCGGTCGCACTGACTGAGGACAGACGCCTG AGTAATTGAAGCAGGGAGTCAGGGTGGGTTTCCAGTCGGTCGCACTGACTGAGGACAGACGCCTG T G SPATC1L Ensembl:ENSG00000160284 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:46184286..46184371 26863410 MeRIP-seq:(Medium) rs116388708 Functional Loss SNV dbSNP153 33..33 33 - - - 62284 RMVar_ID_62284 Human_SNP_ID_696911149 m1A Human chr21 + 46184398 46184398 46184398 TTTCTTGGCTCCGAGGGTCTTGTTTTATCAGCAGCCGGGATGCAACAGATGGGTCATCTCATCCT TTTCTTGGCTCCGAGGGTCTTGTTTTATCAGCCGCCGGGATGCAACAGATGGGTCATCTCATCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46184303..46184400 26863196 MeRIP-seq:(Medium) rs377485135 Functional Loss SNV dbSNP153 33..33 33 - - - 62285 RMVar_ID_62285 Human_SNP_ID_696912801 m1A Human chr21 - 46189596 46189596 46189596 TCCTTCAGGGGCACCCCTCTGCCTTGGTGTGCAGTCCAGGGCTCTCACCCAGGTGCCGCACCCTC TCCTTCAGGGGCACCCCTCTGCCTTGGTGTGCGGTCCAGGGCTCTCACCCAGGTGCCGCACCCTC T C LSS Ensembl:ENSG00000160285 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14356043,Human_RBP_ID_26496089 Human_miRNA_ID_130642,Human_miRNA_ID_620882,Human_miRNA_ID_1148629,Human_miRNA_ID_1228783,Human_miRNA_ID_1981411,Human_miRNA_ID_1983135,Human_miRNA_ID_2510002,Human_miRNA_ID_2542726,Human_miRNA_ID_2544591,Human_miRNA_ID_2546429,Human_miRNA_ID_2548295,Human_miRNA_ID_2550159,Human_miRNA_ID_2552028,Human_miRNA_ID_2557441,Human_miRNA_ID_2559327,Human_miRNA_ID_2589741 GWAS_ID_7631,GWAS_ID_7632,GWAS_ID_7633,GWAS_ID_7634 RMVar_hsa_circ_112693,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_123146,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212705,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_212706 62286 RMVar_ID_62286 Human_SNP_ID_696913172 m1A Human chr21 + 46190755 46190755 46190755 GGAATCACACAGGCACAGCTGCTCCTCTCCCAAGAACTCAGCTATTGGTCAGAAAAAACCTCCTA GGAATCACACAGGCACAGCTGCTCCTCTCCCAGGAACTCAGCTATTGGTCAGAAAAAACCTCCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46190640..46190945 26863196 MeRIP-seq:(Medium) rs576936359 Functional Loss SNV dbSNP153 33..33 33 - - - 62287 RMVar_ID_62287 Human_SNP_ID_696914760 m1A Human chr21 + 46194580 46194579 46194581 CTCTGCAAATAACGCCGCTCCTCGCAGGACTCAAAGTCCTCCCCCCAGCCTCCGTCTGCCATCTG CTCTGCAAATAACGCCGCTCCTCGCAGGACTC__AGTCCTCCCCCCAGCCTCCGTCTGCCATCTG CAA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46194529..46196239 32194978 MeRIP-seq:(Medium) rs748058367 Functional Loss DEL dbSNP153 33..34 33 - - - 62288 RMVar_ID_62288 Human_SNP_ID_696914761 m1A Human chr21 + 46194580 46194580 46194580 CTCTGCAAATAACGCCGCTCCTCGCAGGACTCAAAGTCCTCCCCCCAGCCTCCGTCTGCCATCTG CTCTGCAAATAACGCCGCTCCTCGCAGGACTCGAAGTCCTCCCCCCAGCCTCCGTCTGCCATCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46194529..46196239 32194978 MeRIP-seq:(Medium) rs775078203 Functional Loss SNV dbSNP153 33..33 33 - - - 62289 RMVar_ID_62289 Human_SNP_ID_696914762 m1A Human chr21 + 46194580 46194580 46194580 CTCTGCAAATAACGCCGCTCCTCGCAGGACTCAAAGTCCTCCCCCCAGCCTCCGTCTGCCATCTG CTCTGCAAATAACGCCGCTCCTCGCAGGACTCTAAGTCCTCCCCCCAGCCTCCGTCTGCCATCTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46194529..46196239 32194978 MeRIP-seq:(Medium) rs775078203 Functional Loss SNV dbSNP153 33..33 33 - - - 62290 RMVar_ID_62290 Human_SNP_ID_696918450 m1A Human chr21 - 46207579 46207579 46207579 CCCCCAGCCTGGAGTCATGGCTTGTGCTCTGCAGGGTGGCTTCTCCTTCAGTACGCTGGACTGCG CCCCCAGCCTGGAGTCATGGCTTGTGCTCTGCCGGGTGGCTTCTCCTTCAGTACGCTGGACTGCG T G LSS Ensembl:ENSG00000160285 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:46207551..46207600 32194978 MeRIP-seq:(Medium) rs747998453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387044,Human_RBP_ID_21984645,Human_RBP_ID_22673233,Human_RBP_ID_23212663 RMVar_hsa_circ_112693,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_123146,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212705,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_212706,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709,RMVar_hsa_circ_212711,RMVar_hsa_circ_78546,RMVar_hsa_circ_122251,RMVar_hsa_circ_85662,RMVar_hsa_circ_212713,RMVar_hsa_circ_59149,RMVar_hsa_circ_212712,RMVar_hsa_circ_94593,RMVar_hsa_circ_212714 62291 RMVar_ID_62291 Human_SNP_ID_696920890 m1A Human chr21 - 46215253 46215253 46215253 GTATGAGCACCACCACAGTGCCCACCTGCGGCAGCGGGCCGTGCAGAAGCTGTATGAACACATTG GTATGAGCACCACCACAGTGCCCACCTGCGGCTGCGGGCCGTGCAGAAGCTGTATGAACACATTG T A LSS Ensembl:ENSG00000160285 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46215186..46215286 32194978 MeRIP-seq:(Medium) rs1477029602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10161,Human_RBP_ID_3961398,Human_RBP_ID_5201854,Human_RBP_ID_5386145,Human_RBP_ID_9391876,Human_RBP_ID_14357018,Human_RBP_ID_19006915,Human_RBP_ID_26495862 Human_Splice_Rec_2132082,Human_Splice_Rec_2132083,Human_Splice_Rec_2132130,Human_Splice_Rec_2132131,Human_Splice_Rec_2132174,Human_Splice_Rec_2132175,Human_Splice_Rec_2132218,Human_Splice_Rec_2132219 RMVar_hsa_circ_35839,RMVar_hsa_circ_112693,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_123146,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212705,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_212706,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709,RMVar_hsa_circ_212711,RMVar_hsa_circ_78546,RMVar_hsa_circ_59149,RMVar_hsa_circ_94593,RMVar_hsa_circ_212714,RMVar_hsa_circ_33263,RMVar_hsa_circ_19977,RMVar_hsa_circ_25287,RMVar_hsa_circ_79217,RMVar_hsa_circ_17984,RMVar_hsa_circ_212715 62292 RMVar_ID_62292 Human_SNP_ID_696922205 m1A Human chr21 + 46219246 46219246 46219246 CACCCAGCCCTGCCTGCAGCCTGACTCGGGGTACCTCCATCCATGGCACAGCCTTCTTCCTGCTC CACCCAGCCCTGCCTGCAGCCTGACTCGGGGTCCCTCCATCCATGGCACAGCCTTCTTCCTGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46219244..46219467 26863196 MeRIP-seq:(Medium) rs909332546 Functional Loss SNV dbSNP153 33..33 33 - - - 62293 RMVar_ID_62293 Human_SNP_ID_696922296 m1A Human chr21 - 46219498 46219498 46219498 CTGTCCTGAATGTTTACAGCTGGGAAGGCCTCAATACCCTGTTCCCAGAGATGTGGTATGTCTGC CTGTCCTGAATGTTTACAGCTGGGAAGGCCTCTATACCCTGTTCCCAGAGATGTGGTATGTCTGC T A LSS Ensembl:ENSG00000160285 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46215771..46219568 32194978 MeRIP-seq:(Medium) rs754230211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961401,Human_RBP_ID_19006920 Human_Splice_Rec_2132076,Human_Splice_Rec_2132077,Human_Splice_Rec_2132124,Human_Splice_Rec_2132125,Human_Splice_Rec_2132168,Human_Splice_Rec_2132169,Human_Splice_Rec_2132212,Human_Splice_Rec_2132213,Human_Splice_Rec_2132254,Human_Splice_Rec_2132255,Human_Splice_Rec_2132268,Human_Splice_Rec_2132269 Human_miRNA_ID_2425857,Human_miRNA_ID_2425858,Human_miRNA_ID_2435527,Human_miRNA_ID_2435528 Clinvar_Rec_225 GWAS_ID_7635 RMVar_hsa_circ_35839,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709,RMVar_hsa_circ_212711,RMVar_hsa_circ_78546,RMVar_hsa_circ_59149,RMVar_hsa_circ_94593,RMVar_hsa_circ_212714,RMVar_hsa_circ_33263,RMVar_hsa_circ_48355,RMVar_hsa_circ_19977,RMVar_hsa_circ_17984 62294 RMVar_ID_62294 Human_SNP_ID_696922297 m1A Human chr21 - 46219498 46219498 46219498 CTGTCCTGAATGTTTACAGCTGGGAAGGCCTCAATACCCTGTTCCCAGAGATGTGGTATGTCTGC CTGTCCTGAATGTTTACAGCTGGGAAGGCCTCGATACCCTGTTCCCAGAGATGTGGTATGTCTGC T C LSS Ensembl:ENSG00000160285 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46215771..46219568 32194978 MeRIP-seq:(Medium) rs754230211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961401,Human_RBP_ID_19006920 Human_Splice_Rec_2132076,Human_Splice_Rec_2132077,Human_Splice_Rec_2132124,Human_Splice_Rec_2132125,Human_Splice_Rec_2132168,Human_Splice_Rec_2132169,Human_Splice_Rec_2132212,Human_Splice_Rec_2132213,Human_Splice_Rec_2132254,Human_Splice_Rec_2132255,Human_Splice_Rec_2132268,Human_Splice_Rec_2132269 Human_miRNA_ID_2425857,Human_miRNA_ID_2425858,Human_miRNA_ID_2435527,Human_miRNA_ID_2435528 Clinvar_Rec_225 GWAS_ID_7635 RMVar_hsa_circ_35839,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709,RMVar_hsa_circ_212711,RMVar_hsa_circ_78546,RMVar_hsa_circ_59149,RMVar_hsa_circ_94593,RMVar_hsa_circ_212714,RMVar_hsa_circ_33263,RMVar_hsa_circ_48355,RMVar_hsa_circ_19977,RMVar_hsa_circ_17984 62295 RMVar_ID_62295 Human_SNP_ID_696924719 m1A Human chr21 - 46227677 46227677 46227677 TTTTTCGATCTCTTTGCAGAAGAATTACTTTAAGGACTTGCCCAAAGCCCACACCGCCTTTGAGG TTTTTCGATCTCTTTGCAGAAGAATTACTTTATGGACTTGCCCAAAGCCCACACCGCCTTTGAGG T A LSS Ensembl:ENSG00000160285 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46227530..46227716 26863196 MeRIP-seq:(Medium) rs772160065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961407,Human_RBP_ID_4683197,Human_RBP_ID_7053892,Human_RBP_ID_9391556,Human_RBP_ID_14357421 Human_Splice_Rec_2132070,Human_Splice_Rec_2132118,Human_Splice_Rec_2132162,Human_Splice_Rec_2132206,Human_Splice_Rec_2132248,Human_Splice_Rec_2132262,Human_Splice_Rec_2132274 RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_98025,RMVar_hsa_circ_212708,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709 62296 RMVar_ID_62296 Human_SNP_ID_696925021 m1A Human chr21 + 46228541 46228541 46228541 CGTCTGCCGGCCCCTCTCGCAGTTGAGTCGCCAGCGGCCGAGGTCGGTGGCGGGCTCGGTCTTGT CGTCTGCCGGCCCCTCTCGCAGTTGAGTCGCCGGCGGCCGAGGTCGGTGGCGGGCTCGGTCTTGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46228496..46228751 26863196 MeRIP-seq:(Medium) rs1287103323 Functional Loss SNV dbSNP153 33..33 33 - - - 62297 RMVar_ID_62297 Human_SNP_ID_696925493 m1A Human chr21 - 46229278 46229278 46229278 ACCCGCGGCTGGACCCTCCTCACAAATTTCTCAGAGAGGCTCACCTCAAAGCGCGGCGCACGAGG ACCCGCGGCTGGACCCTCCTCACAAATTTCTCGGAGAGGCTCACCTCAAAGCGCGGCGCACGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46229262..46229451 26863196 MeRIP-seq:(Medium) rs1345571816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8544607 62298 RMVar_ID_62298 Human_SNP_ID_696925496 m1A Human chr21 + 46229294 46229294 46229294 TTGAGGTGAGCCTCTCTGAGAAATTTGTGAGGAGGGTCCAGCCGCGGGTCGGAAGGAAGGACGTG TTGAGGTGAGCCTCTCTGAGAAATTTGTGAGGGGGGTCCAGCCGCGGGTCGGAAGGAAGGACGTG A G MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46229246..46229576 26863196 MeRIP-seq:(Medium) rs1290919435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928442,Human_RBP_ID_19110482,Human_RBP_ID_24553695 Human_Splice_Rec_2132329,Human_Splice_Rec_2132331,Human_Splice_Rec_2132335 62299 RMVar_ID_62299 Human_SNP_ID_696934222 m1A Human chr21 - 46260865 46260865 46260865 AGAGAGAGAGCTGGTGTTAAGTGAGCTGAGCCAGGGCCTGGCCGTGGAGCTGATGGAACGCGTGA AGAGAGAGAGCTGGTGTTAAGTGAGCTGAGCCGGGGCCTGGCCGTGGAGCTGATGGAACGCGTGA T C MCM3AP Ensembl:ENSG00000160294 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46260776..46260952 26863196 MeRIP-seq:(Medium) rs186506332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245266,Human_RBP_ID_927642,Human_RBP_ID_3961423,Human_RBP_ID_4678369,Human_RBP_ID_5529625,Human_RBP_ID_8860776,Human_RBP_ID_9299564,Human_RBP_ID_9332317,Human_RBP_ID_14359028,Human_RBP_ID_19007464,Human_RBP_ID_23009731,Human_RBP_ID_23932154 Human_Splice_Rec_2132372,Human_Splice_Rec_2132373,Human_Splice_Rec_2132408,Human_Splice_Rec_2132409,Human_Splice_Rec_2132460,Human_Splice_Rec_2132461,Human_Splice_Rec_2132516,Human_Splice_Rec_2132517 Human_miRNA_ID_2084573,Human_miRNA_ID_2270715 RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_212721,RMVar_hsa_circ_99167,RMVar_hsa_circ_16772,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_268669,RMVar_hsa_circ_19974,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_333797,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_31284,RMVar_hsa_circ_31919,RMVar_hsa_circ_212725,RMVar_hsa_circ_23958 62300 RMVar_ID_62300 Human_SNP_ID_696934238 m1A Human chr21 + 46260905 46260905 46260905 CTCACTTAACACCAGCTCTCTCTCTTGTTTCAACCTACAGGGAAGAGAAAAAATACACAAGGGTA CTCACTTAACACCAGCTCTCTCTCTTGTTTCAGCCTACAGGGAAGAGAAAAAATACACAAGGGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:46260801..46260939;chr21:46260776..46260925;chr21:46260776..46260949 26863196 MeRIP-seq:(Medium) rs191354648 Functional Loss SNV dbSNP153 33..33 33 - - - 62301 RMVar_ID_62301 Human_SNP_ID_696934344 m1A Human chr21 + 46261243 46261243 46261243 GCTAGGGTCAGTTCTTGCCTGTGTCCACACTGAGCTCCTTATTCGGCTGCATGGACAAGACACAC GCTAGGGTCAGTTCTTGCCTGTGTCCACACTGCGCTCCTTATTCGGCTGCATGGACAAGACACAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46261240..46261375 26863196 MeRIP-seq:(Medium) rs753335591 Functional Loss SNV dbSNP153 33..33 33 - - - 62302 RMVar_ID_62302 Human_SNP_ID_696942068 m1A Human chr21 + 46285906 46285906 46285906 CTCGAGCGGGCTGGAAGGACGAGGGCGCTGCCACGAAGCTGAGGCCTCTCGGCGGGGACGGCGTG CTCGAGCGGGCTGGAAGGACGAGGGCGCTGCCGCGAAGCTGAGGCCTCTCGGCGGGGACGGCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46285856..46285963 26863196 MeRIP-seq:(Medium) rs1029001853 Functional Loss SNV dbSNP153 33..33 33 - - - 62303 RMVar_ID_62303 Human_SNP_ID_696942151 m1A Human chr21 + 46286162 46286162 46286162 CGGCCCAGCCCCCACGCTCACCGTCTCGCCCCAGGACCCCGAGGCCCGCGCTGCCCACTGGCCCC CGGCCCAGCCCCCACGCTCACCGTCTCGCCCCCGGACCCCGAGGCCCGCGCTGCCCACTGGCCCC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:46286044..46286177 26863196 MeRIP-seq:(Medium) rs1263413878 Functional Loss SNV dbSNP153 33..33 33 - - - 62304 RMVar_ID_62304 Human_SNP_ID_696942405 m1A Human chr21 - 46286680 46286678 46286681 TCTATGGAAGGATGCCGCGGAATCCGGCCAGAAGGACTCCAGGCGGGCGGAGCGGAAGGAGCGGT TCTATGGAAGGATGCCGCGGAATCCGGCCAG___GACTCCAGGCGGGCGGAGCGGAAGGAGCGGT CCTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46286678..46286902 26863196 MeRIP-seq:(Medium) rs539766944 Functional Loss DEL dbSNP153 32..34 33 - - - Clinvar_Rec_226,Clinvar_Rec_227 62305 RMVar_ID_62305 Human_SNP_ID_696942406 m1A Human chr21 - 46286680 46286680 46286680 TCTATGGAAGGATGCCGCGGAATCCGGCCAGAAGGACTCCAGGCGGGCGGAGCGGAAGGAGCGGT TCTATGGAAGGATGCCGCGGAATCCGGCCAGATGGACTCCAGGCGGGCGGAGCGGAAGGAGCGGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46286678..46286902 26863196 MeRIP-seq:(Medium) rs1400882416 Functional Loss SNV dbSNP153 33..33 33 - - - 62306 RMVar_ID_62306 Human_SNP_ID_696942498 m1A Human chr21 + 46286953 46286953 46286953 TGGTGATTAGAAATCTGCAGCGAGTCATCCCCATCAGGAGAGCGCCACTTCGCAGTAAGATCGAG TGGTGATTAGAAATCTGCAGCGAGTCATCCCCGTCAGGAGAGCGCCACTTCGCAGTAAGATCGAG A G YBEY Ensembl:ENSG00000182362 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46286903..46286974 26863196 MeRIP-seq:(Medium) rs373749634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_574332,Human_RBP_ID_1938994,Human_RBP_ID_4678584,Human_RBP_ID_26821892 Human_Splice_Rec_2132560,Human_Splice_Rec_2132568,Human_Splice_Rec_2132572,Human_Splice_Rec_2132573,Human_Splice_Rec_2132580,Human_Splice_Rec_2132588,Human_Splice_Rec_2132594,Human_Splice_Rec_2132595,Human_Splice_Rec_2132600,Human_Splice_Rec_2132604 RMVar_hsa_circ_77535,RMVar_hsa_circ_212736 62307 RMVar_ID_62307 Human_SNP_ID_696946013 m1A Human chr21 - 46296232 46296232 46296232 ACCCCCTCGGTAGTGGGATGGATGGGCTCCTTACCTGCTGCCACTCTGCCTCCGTGCCGTGTGTG ACCCCCTCGGTAGTGGGATGGATGGGCTCCTTTCCTGCTGCCACTCTGCCTCCGTGCCGTGTGTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46296216..46296281 26863196 MeRIP-seq:(Medium) rs1386075890 Functional Loss SNV dbSNP153 33..33 33 - - - 62308 RMVar_ID_62308 Human_SNP_ID_696946014 m1A Human chr21 - 46296232 46296232 46296232 ACCCCCTCGGTAGTGGGATGGATGGGCTCCTTACCTGCTGCCACTCTGCCTCCGTGCCGTGTGTG ACCCCCTCGGTAGTGGGATGGATGGGCTCCTTGCCTGCTGCCACTCTGCCTCCGTGCCGTGTGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46296216..46296281 26863196 MeRIP-seq:(Medium) rs1386075890 Functional Loss SNV dbSNP153 33..33 33 - - - 62309 RMVar_ID_62309 Human_SNP_ID_696954638 m1A Human chr21 + 46323146 46323146 46323146 TTAGTTTCCCAAGTTCCACCTACGCGCGCGCCAGCTGAGAAAACGCCCACCCCGGCGGTCCCGCC TTAGTTTCCCAAGTTCCACCTACGCGCGCGCCCGCTGAGAAAACGCCCACCCCGGCGGTCCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46323095..46323213 26863196 MeRIP-seq:(Medium) rs1300574960 Functional Loss SNV dbSNP153 33..33 33 - - - 62310 RMVar_ID_62310 Human_SNP_ID_696954771 m1A Human chr21 - 46323499 46323499 46323499 AACTCGGCCGAATGCGGTCAGAAAGCCCGCGAACCGCCTGGACCTGCAGGCCCCGCCGCTTGGAG AACTCGGCCGAATGCGGTCAGAAAGCCCGCGACCCGCCTGGACCTGCAGGCCCCGCCGCTTGGAG T G C21orf58 Ensembl:ENSG00000160298 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46323455..46323599 26863196 MeRIP-seq:(Medium) rs932758245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245488,Human_RBP_ID_14361676,Human_RBP_ID_22083267,Human_RBP_ID_22362256,Human_RBP_ID_25649395 62311 RMVar_ID_62311 Human_SNP_ID_696954773 m1A Human chr21 - 46323510 46323510 46323510 CTTCAGAGAAGAACTCGGCCGAATGCGGTCAGAAAGCCCGCGAACCGCCTGGACCTGCAGGCCCC CTTCAGAGAAGAACTCGGCCGAATGCGGTCAGCAAGCCCGCGAACCGCCTGGACCTGCAGGCCCC T G C21orf58 Ensembl:ENSG00000160298 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46323460..46323551 26863196 MeRIP-seq:(Medium) rs1398303068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245488,Human_RBP_ID_14361676,Human_RBP_ID_27030373 62312 RMVar_ID_62312 Human_SNP_ID_696955056 m1A Human chr21 + 46324196 46324196 46324196 TAGAGCGAAGGCTGCTCTGTGTCAGCCCCGTCACCGCCGGGCGGCCCGCGCGGAGTCTGAGGGAG TAGAGCGAAGGCTGCTCTGTGTCAGCCCCGTCGCCGCCGGGCGGCCCGCGCGGAGTCTGAGGGAG A G PCNT Ensembl:ENSG00000160299 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46324151..46324926 26863196 MeRIP-seq:(Medium) rs755311284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4678797,Human_RBP_ID_8860806,Human_RBP_ID_9299395,Human_RBP_ID_18423379,Human_RBP_ID_21896163 Human_Splice_Rec_2132731,Human_Splice_Rec_2132745 62313 RMVar_ID_62313 Human_SNP_ID_696956080 m1A Human chr21 + 46326429 46326429 46326429 AAAAACAAAAGGTGACAGTTCGCATTCGGAGAAAAAGACGGCGAAGAGGAAGGGCTCGGCTGTCG AAAAACAAAAGGTGACAGTTCGCATTCGGAGAGAAAGACGGCGAAGAGGAAGGGCTCGGCTGTCG A G AP000471.1,PCNT Ensembl:ENSG00000286224,Ensembl:ENSG00000160299 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr21:46326336..46334398;chr21:46326321..46326536 26863196 MeRIP-seq:(Medium) rs1309693926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14361758,Human_RBP_ID_23932326 Human_Splice_Rec_2132732,Human_Splice_Rec_2132746,Human_Splice_Rec_2132838 RMVar_hsa_circ_64540,RMVar_hsa_circ_212742,RMVar_hsa_circ_120731,RMVar_hsa_circ_290005,RMVar_hsa_circ_356146,RMVar_hsa_circ_358615,RMVar_hsa_circ_285237,RMVar_hsa_circ_10467,RMVar_hsa_circ_52454,RMVar_hsa_circ_59616,RMVar_hsa_circ_41597,RMVar_hsa_circ_212743 62314 RMVar_ID_62314 Human_SNP_ID_696958932 m1A Human chr21 + 46334727 46334727 46334727 ACCACACACCAGAACAGCGTGGGATCTTCACAATCAGTGACCACCCAGCAGAACAGCGTGGGATG ACCACACACCAGAACAGCGTGGGATCTTCACAGTCAGTGACCACCCAGCAGAACAGCGTGGGATG A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs766375190 Functional Loss SNV dbSNP153 33..33 33 - - - 62315 RMVar_ID_62315 Human_SNP_ID_696958933 m1A Human chr21 + 46334727 46334727 46334727 ACCACACACCAGAACAGCGTGGGATCTTCACAATCAGTGACCACCCAGCAGAACAGCGTGGGATG ACCACACACCAGAACAGCGTGGGATCTTCACATTCAGTGACCACCCAGCAGAACAGCGTGGGATG A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs766375190 Functional Loss SNV dbSNP153 33..33 33 - - - 62316 RMVar_ID_62316 Human_SNP_ID_696963004 m1A Human chr21 - 46348234 46348234 46348234 ACGCAAGGCCTAATCCACACAGTCACCCTCAAAGCGTTAGTAATACATCTCCCTATAAGTCCCAG ACGCAAGGCCTAATCCACACAGTCACCCTCAATGCGTTAGTAATACATCTCCCTATAAGTCCCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46348232..46348315 26863196 MeRIP-seq:(Medium) rs1013595248 Functional Loss SNV dbSNP153 33..33 33 - - - 62317 RMVar_ID_62317 Human_SNP_ID_696976366 m1A Human chr21 - 46385962 46385962 46385962 GACACACTGACCTTTCGCTGTGGGACAGGTTGACGTCGGCCTTGAGCATGGAGAGGAGGTTTGCG GACACACTGACCTTTCGCTGTGGGACAGGTTGGCGTCGGCCTTGAGCATGGAGAGGAGGTTTGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46381778..46389340 32194978 MeRIP-seq:(Medium) rs762148129 Functional Loss SNV dbSNP153 33..33 33 - - - 62318 RMVar_ID_62318 Human_SNP_ID_696978030 m1A Human chr21 - 46390776 46390776 46390776 CCAGCTCTGCCTTTGCTGCGCTCTCCTCCTTCAAACACTCCAGCAGCTCCTGGTGCTTCCTGACA CCAGCTCTGCCTTTGCTGCGCTCTCCTCCTTCCAACACTCCAGCAGCTCCTGGTGCTTCCTGACA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:46390726..46391357 26863196 MeRIP-seq:(Medium) rs1298142341 Functional Loss SNV dbSNP153 33..33 33 - - - 62319 RMVar_ID_62319 Human_SNP_ID_696980136 m1A Human chr21 - 46397494 46397494 46397494 ATGCAAAAAAATGTATTATTCAGAATTCTTACATCCATGAATTGCCGCTGGTTGCGCAAATGCTT ATGCAAAAAAATGTATTATTCAGAATTCTTACCTCCATGAATTGCCGCTGGTTGCGCAAATGCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46397444..46401704 32194978 MeRIP-seq:(Medium) rs767410674 Functional Loss SNV dbSNP153 33..33 33 - - - 62320 RMVar_ID_62320 Human_SNP_ID_696985413 m1A Human chr21 - 46413253 46413194 46413253 GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCACGCCTTCCCCCTCCCCACACCTTGCTGCTGCG GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTC_________________________________ CGAGGCCCACCCGGGAGAGGCTGGACACGCAGCAGCAAGGTGTGGGGAGGGGGAAGGCGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46413208..46413275 26863196 MeRIP-seq:(Medium) rs1569272388 Functional Loss DEL dbSNP153 33..65 33 - - - 62321 RMVar_ID_62321 Human_SNP_ID_696985453 m1A Human chr21 - 46413253 46413253 46413253 GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCACGCCTTCCCCCTCCCCACACCTTGCTGCTGCG GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCTCGCCTTCCCCCTCCCCACACCTTGCTGCTGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46413208..46413275 26863196 MeRIP-seq:(Medium) rs13050327 Functional Loss SNV dbSNP153 33..33 33 - - - 62322 RMVar_ID_62322 Human_SNP_ID_696985454 m1A Human chr21 - 46413253 46413253 46413253 GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCACGCCTTCCCCCTCCCCACACCTTGCTGCTGCG GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCGCGCCTTCCCCCTCCCCACACCTTGCTGCTGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46413208..46413275 26863196 MeRIP-seq:(Medium) rs13050327 Functional Loss SNV dbSNP153 33..33 33 - - - 62323 RMVar_ID_62323 Human_SNP_ID_696985455 m1A Human chr21 - 46413253 46413253 46413253 GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCACGCCTTCCCCCTCCCCACACCTTGCTGCTGCG GCCGCGTGTCCAGCCTCTCCCAGGGGGGCCTCCCGCCTTCCCCCTCCCCACACCTTGCTGCTGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46413208..46413275 26863196 MeRIP-seq:(Medium) rs13050327 Functional Loss SNV dbSNP153 33..33 33 - - - 62324 RMVar_ID_62324 Human_SNP_ID_696986935 m1A Human chr21 + 46416758 46416758 46416758 CAGACCCAGGGGCCGGGGCTGCTTTGTTCCCCAGGCGTGTCTGCAGCAGCGCTGGCACTGCAGTG CAGACCCAGGGGCCGGGGCTGCTTTGTTCCCCTGGCGTGTCTGCAGCAGCGCTGGCACTGCAGTG A T PCNT Ensembl:ENSG00000160299 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46416506..46416806 32194978 MeRIP-seq:(Medium) rs1249350066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3664967,Human_RBP_ID_22083278,Human_RBP_ID_27030509 Human_Splice_Rec_2132803,Human_Splice_Rec_2132895 RMVar_hsa_circ_57716,RMVar_hsa_circ_65299,RMVar_hsa_circ_42707,RMVar_hsa_circ_30224,RMVar_hsa_circ_212756,RMVar_hsa_circ_371395,RMVar_hsa_circ_47853,RMVar_hsa_circ_324163,RMVar_hsa_circ_23620 62325 RMVar_ID_62325 Human_SNP_ID_696991533 m1A Human chr21 + 46430127 46430127 46430127 AAACAGCGTGCAGAAGCTCCTGGCGGCGGAGCAGACTGTAGTGCGAGATTTGAAGTCCGACCTCT AAACAGCGTGCAGAAGCTCCTGGCGGCGGAGCCGACTGTAGTGCGAGATTTGAAGTCCGACCTCT A C PCNT Ensembl:ENSG00000160299 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:46430076..46431595;chr21:46430076..46430627 26863196 MeRIP-seq:(Medium) rs141449534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151003,Human_RBP_ID_1939158,Human_RBP_ID_8860487,Human_RBP_ID_14364914,Human_RBP_ID_23009402 Human_miRNA_ID_2054306 RMVar_hsa_circ_6618,RMVar_hsa_circ_40539 62326 RMVar_ID_62326 Human_SNP_ID_696991722 m1A Human chr21 + 46430574 46430574 46430574 CCGCGCTTCAGGAGCTGGAGAGTGAGCAGGGGAAGGGGCGTGCCCTGCAGAGCCAGCTGGAGGAG CCGCGCTTCAGGAGCTGGAGAGTGAGCAGGGGCAGGGGCGTGCCCTGCAGAGCCAGCTGGAGGAG A C PCNT Ensembl:ENSG00000160299 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46430202..46430630 26863196 MeRIP-seq:(Medium) rs1400666825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64286,Human_RBP_ID_3961853,Human_RBP_ID_19006957,Human_RBP_ID_26344828 Human_Splice_Rec_2132816,Human_Splice_Rec_2132817,Human_Splice_Rec_2132908,Human_Splice_Rec_2132909 RMVar_hsa_circ_6618,RMVar_hsa_circ_40539 62327 RMVar_ID_62327 Human_SNP_ID_696992231 m1A Human chr21 - 46431936 46431936 46431936 CTCCTGAGCGCCTCACAGTGCTTCTGAGCCTCAGCCTCAAGCTGCTGCTGAGAATGCAGGGCTTG CTCCTGAGCGCCTCACAGTGCTTCTGAGCCTCCGCCTCAAGCTGCTGCTGAGAATGCAGGGCTTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46431625..46435962 32194978 MeRIP-seq:(Medium) rs1459283879 Functional Loss SNV dbSNP153 33..33 33 - - - 62328 RMVar_ID_62328 Human_SNP_ID_697026204 m1A Human chr21 + 46554669 46554669 46554669 CGGCCCCCGCACCCTCAGAACCTCGGCACCACACTGCCCACCGTCAAGATGATCGTGGAGGTGCG CGGCCCCCGCACCCTCAGAACCTCGGCACCACGCTGCCCACCGTCAAGATGATCGTGGAGGTGCG A G DIP2A Ensembl:ENSG00000160305 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1107065 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19007531 Human_Splice_Rec_2133010,Human_Splice_Rec_2133011,Human_Splice_Rec_2133082,Human_Splice_Rec_2133083,Human_Splice_Rec_2133156,Human_Splice_Rec_2133157,Human_Splice_Rec_2133352,Human_Splice_Rec_2133353 RMVar_hsa_circ_87161,RMVar_hsa_circ_88895,RMVar_hsa_circ_212779,RMVar_hsa_circ_212780,RMVar_hsa_circ_48607,RMVar_hsa_circ_32019,RMVar_hsa_circ_17715,RMVar_hsa_circ_1432,RMVar_hsa_circ_106334,RMVar_hsa_circ_112209,RMVar_hsa_circ_212781,RMVar_hsa_circ_212783 62329 RMVar_ID_62329 Human_SNP_ID_697047124 m1A Human chr21 - 46635715 46635715 46635715 CGCTGAGTTCCGCGTCCACACCGCCAGCGCGGAGGGGTGGACGGTCCTTTCCAGGAGCCTGAGCC CGCTGAGTTCCGCGTCCACACCGCCAGCGCGGCGGGGTGGACGGTCCTTTCCAGGAGCCTGAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46635651..46635814 26863196 MeRIP-seq:(Medium) rs1022069221 Functional Loss SNV dbSNP153 33..33 33 - - - 62330 RMVar_ID_62330 Human_SNP_ID_697047513 m1A Human chr21 - 46636951 46636951 46636951 TCACTTCTGGGACAGTCACCTGATGTTGCCATAGTTCTCTTAGGCTCTGCCTCATAACTGCTGAT TCACTTCTGGGACAGTCACCTGATGTTGCCATGGTTCTCTTAGGCTCTGCCTCATAACTGCTGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46636868..46636990 26863196 MeRIP-seq:(Medium) rs1298074768 Functional Loss SNV dbSNP153 33..33 33 - - - 62331 RMVar_ID_62331 Human_SNP_ID_697050593 m1A Human chr21 + 46648483 46648483 46648483 CTTCCAGAAACTCCACTTGGAGATGTTGGCAGACCAGCCACGAACAACTAAATACCACAGTGTCA CTTCCAGAAACTCCACTTGGAGATGTTGGCAGCCCAGCCACGAACAACTAAATACCACAGTGTCA A C PRMT2 Ensembl:ENSG00000160310 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46648449..46649841 32194978 MeRIP-seq:(Medium) rs749647394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927675,Human_RBP_ID_22673288,Human_RBP_ID_26821894 Human_Splice_Rec_2133404,Human_Splice_Rec_2133418,Human_Splice_Rec_2133432,Human_Splice_Rec_2133452,Human_Splice_Rec_2133464,Human_Splice_Rec_2133484,Human_Splice_Rec_2133496,Human_Splice_Rec_2133508,Human_Splice_Rec_2133528,Human_Splice_Rec_2133540,Human_Splice_Rec_2133550,Human_Splice_Rec_2133556,Human_Splice_Rec_2133562 Human_miRNA_ID_2455965,Human_miRNA_ID_2455966,Human_miRNA_ID_2455967,Human_miRNA_ID_2533480,Human_miRNA_ID_2533481,Human_miRNA_ID_2533482 RMVar_hsa_circ_100531,RMVar_hsa_circ_78656,RMVar_hsa_circ_94649,RMVar_hsa_circ_212785,RMVar_hsa_circ_212786,RMVar_hsa_circ_110991,RMVar_hsa_circ_212787,RMVar_hsa_circ_212788,RMVar_hsa_circ_332109,RMVar_hsa_circ_338782,RMVar_hsa_circ_333584,RMVar_hsa_circ_107943,RMVar_hsa_circ_33088,RMVar_hsa_circ_352687,RMVar_hsa_circ_327112,RMVar_hsa_circ_212793 62332 RMVar_ID_62332 Human_SNP_ID_697050622 m1A Human chr21 - 46648568 46648568 46648568 TGTGCACAGAAGAGACTGATGATCCCAGTCCCACAGCCCACGTCCAGGATGACTTTATCCGTCAG TGTGCACAGAAGAGACTGATGATCCCAGTCCCGCAGCCCACGTCCAGGATGACTTTATCCGTCAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:46648526..46648682 26863196 MeRIP-seq:(Medium) rs755628784 Functional Loss SNV dbSNP153 33..33 33 - - - 62333 RMVar_ID_62333 Human_SNP_ID_697050958 m1A Human chr21 - 46649648 46649645 46649648 CATCCTCCACCTTCTGCTGGTACACGGTGATGATGTCAGCAAAGCCGTTCTGCAGGACCAGCTGC CATCCTCCACCTTCTGCTGGTACACGGTGATG___TCAGCAAAGCCGTTCTGCAGGACCAGCTGC ACAT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:46649576..46649650 32194978 MeRIP-seq:(Medium) rs770083049 Functional Loss DEL dbSNP153 33..35 33 - - - 62334 RMVar_ID_62334 Human_SNP_ID_697051248 m1A Human chr21 + 46650702 46650701 46650702 CCCCGGCCACGGGGACAAAAAGAGGACAGAGCAGGAGTGAGGCTGTGGTGAGGCCAAGGTTGTGT CCCCGGCCACGGGGACAAAAAGAGGACAGAGC_GGAGTGAGGCTGTGGTGAGGCCAAGGTTGTGT CA C PRMT2 Ensembl:ENSG00000160310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46650697..46651570 26863196 MeRIP-seq:(Medium) rs1316623264 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7055037,Human_RBP_ID_14369323 RMVar_hsa_circ_78656,RMVar_hsa_circ_94649,RMVar_hsa_circ_212785,RMVar_hsa_circ_212786,RMVar_hsa_circ_110991,RMVar_hsa_circ_212788,RMVar_hsa_circ_332109,RMVar_hsa_circ_338782,RMVar_hsa_circ_107943,RMVar_hsa_circ_33088,RMVar_hsa_circ_352687,RMVar_hsa_circ_212793 62335 RMVar_ID_62335 Human_SNP_ID_697051259 m1A Human chr21 + 46650752 46650752 46650752 AGGCCAAGGTTGTGTGGGCGGTGATACGGGGAAGCCTGGCTGCTGGAGTGTCCGGCTGTGCCCTG AGGCCAAGGTTGTGTGGGCGGTGATACGGGGAGGCCTGGCTGCTGGAGTGTCCGGCTGTGCCCTG A G PRMT2 Ensembl:ENSG00000160310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:46650732..46651427 26863196 MeRIP-seq:(Medium) rs576271305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832673,Human_RBP_ID_5323663,Human_RBP_ID_7055040,Human_RBP_ID_9432522 RMVar_hsa_circ_78656,RMVar_hsa_circ_94649,RMVar_hsa_circ_212785,RMVar_hsa_circ_212786,RMVar_hsa_circ_110991,RMVar_hsa_circ_212788,RMVar_hsa_circ_332109,RMVar_hsa_circ_338782,RMVar_hsa_circ_107943,RMVar_hsa_circ_33088,RMVar_hsa_circ_352687,RMVar_hsa_circ_212793 62336 RMVar_ID_62336 Human_SNP_ID_697051523 m1A Human chr21 - 46651759 46651759 46651759 TGAAGGTGGGTACAACCGCACCAACGACTCCCAGATTCATACCCTCCCTCCCTCAAATCCGACCA TGAAGGTGGGTACAACCGCACCAACGACTCCCTGATTCATACCCTCCCTCCCTCAAATCCGACCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46651753..46651956 26863196 MeRIP-seq:(Medium) rs752914002 Functional Loss SNV dbSNP153 33..33 33 - - - 62337 RMVar_ID_62337 Human_SNP_ID_697051524 m1A Human chr21 - 46651759 46651759 46651759 TGAAGGTGGGTACAACCGCACCAACGACTCCCAGATTCATACCCTCCCTCCCTCAAATCCGACCA TGAAGGTGGGTACAACCGCACCAACGACTCCCGGATTCATACCCTCCCTCCCTCAAATCCGACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46651753..46651956 26863196 MeRIP-seq:(Medium) rs752914002 Functional Loss SNV dbSNP153 33..33 33 - - - 62338 RMVar_ID_62338 Human_SNP_ID_697053430 m1A Human chr21 - 46659095 46659095 46659095 CATTCTACCCTGCTCTGCCCATCTGTCTTGTTATAGCACCATACTGCTTTAATTACTCCAATGCT CATTCTACCCTGCTCTGCCCATCTGTCTTGTTGTAGCACCATACTGCTTTAATTACTCCAATGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46659091..46659192 32194978 MeRIP-seq:(Medium) rs1315877364 Functional Loss SNV dbSNP153 33..33 33 - - - 62339 RMVar_ID_62339 Human_SNP_ID_697053590 m1A Human chr21 + 46659732 46659732 46659732 GGCATCAGGCTGCCCACCCCAGTCACTGCCAGAGCCTCCCACCTGAGTGTTCCTCCCGGCACTGG GGCATCAGGCTGCCCACCCCAGTCACTGCCAGGGCCTCCCACCTGAGTGTTCCTCCCGGCACTGG A G PRMT2 Ensembl:ENSG00000160310 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46659729..46659835 32194978 MeRIP-seq:(Medium) rs553330158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_574468,Human_RBP_ID_7055094,Human_RBP_ID_8206436,Human_RBP_ID_17208472,Human_RBP_ID_26496105 RMVar_hsa_circ_78656,RMVar_hsa_circ_94649,RMVar_hsa_circ_212785,RMVar_hsa_circ_212786,RMVar_hsa_circ_110991,RMVar_hsa_circ_212788,RMVar_hsa_circ_332109,RMVar_hsa_circ_107943,RMVar_hsa_circ_33088,RMVar_hsa_circ_22631,RMVar_hsa_circ_212793 62340 RMVar_ID_62340 Human_SNP_ID_697053858 m1A Human chr21 - 46660693 46660693 46660693 TGCTAAGCCACTATCTGGGGCCCTGGAACCCCAGAGCAGCCCTCAGGCCTCCACAGGCCCTGGGT TGCTAAGCCACTATCTGGGGCCCTGGAACCCCTGAGCAGCCCTCAGGCCTCCACAGGCCCTGGGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46660690..46660806 32194978 MeRIP-seq:(Medium) rs1207805325 Functional Loss SNV dbSNP153 33..33 33 - - - 62341 RMVar_ID_62341 Human_SNP_ID_118912938 m1A Human chr2 - 240012091 240012088 240012091 TGGAGAGATGCAGGGAGAGTCAGGTGACAAGAAGAGAGTGTGCTGAGGACAGATGGCGGACAGAC TGGAGAGATGCAGGGAGAGTCAGGTGACAAGA___GAGTGTGCTGAGGACAGATGGCGGACAGAC CTCT C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240012040..240012243 26863196 MeRIP-seq:(Medium) rs3838574 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_242730,Human_RBP_ID_6899843,Human_RBP_ID_13817384 RMVar_hsa_circ_12827,RMVar_hsa_circ_207936,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_344547,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_271956,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_312803,RMVar_hsa_circ_338244,RMVar_hsa_circ_291146,RMVar_hsa_circ_295847,RMVar_hsa_circ_207941,RMVar_hsa_circ_207942,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_345598,RMVar_hsa_circ_207946,RMVar_hsa_circ_207947,RMVar_hsa_circ_334768,RMVar_hsa_circ_267376,RMVar_hsa_circ_207948 62342 RMVar_ID_62342 Human_SNP_ID_118914166 m1A Human chr2 + 240016823 240016823 240016823 CCAGTCCTCAGACTTCAGCAGACACTCAGCAGATGCCGACAGGTATCTCCTGCCACCTTGCCATG CCAGTCCTCAGACTTCAGCAGACACTCAGCAGGTGCCGACAGGTATCTCCTGCCACCTTGCCATG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240016820..240017400 26863196 MeRIP-seq:(Medium) rs889020360 Functional Loss SNV dbSNP153 33..33 33 - - - 62343 RMVar_ID_62343 Human_SNP_ID_118914205 m1A Human chr2 - 240016943 240016943 240016943 ACAGTGGGGAGTGGCGTGGACCTGCCCTGGCTAGTGGGCCGCTAAGGGGGAAGGATGCACAGGGG ACAGTGGGGAGTGGCGTGGACCTGCCCTGGCTTGTGGGCCGCTAAGGGGGAAGGATGCACAGGGG T A NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240016941..240017335 26863196 MeRIP-seq:(Medium) rs926140564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8201016,Human_RBP_ID_9429450,Human_RBP_ID_18493928,Human_RBP_ID_18948758 RMVar_hsa_circ_12827,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_344547,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_312803,RMVar_hsa_circ_291146,RMVar_hsa_circ_295847,RMVar_hsa_circ_207941,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_207947,RMVar_hsa_circ_267376,RMVar_hsa_circ_38258 62344 RMVar_ID_62344 Human_SNP_ID_118914440 m1A Human chr2 - 240017831 240017831 240017831 TCAGAGGAAGTACTGTTGATTAATGAAAGAGGAGGCCGAAGCAAGCCAGGTGACCATTCTGTGGA TCAGAGGAAGTACTGTTGATTAATGAAAGAGGTGGCCGAAGCAAGCCAGGTGACCATTCTGTGGA T A NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240017829..240017964 26863196 MeRIP-seq:(Medium) rs1291737002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24379151 Human_Splice_Rec_377640,Human_Splice_Rec_377641 RMVar_hsa_circ_12827,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_344547,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_312803,RMVar_hsa_circ_291146,RMVar_hsa_circ_295847,RMVar_hsa_circ_207941,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_207947,RMVar_hsa_circ_267376,RMVar_hsa_circ_38258 62345 RMVar_ID_62345 Human_SNP_ID_118914679 m1A Human chr2 - 240018558 240018558 240018558 GGAGGCGATGTACAACCAGGGATTCATCCGAAAGCAGTGTGAGTCAGCATTGCAGACCCACTTCT GGAGGCGATGTACAACCAGGGATTCATCCGAATGCAGTGTGAGTCAGCATTGCAGACCCACTTCT T A NDUFA10 Ensembl:ENSG00000130414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:240018551..240018650 32194978 MeRIP-seq:(Medium) rs1012086424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546720,Human_RBP_ID_922445,Human_RBP_ID_3959970,Human_RBP_ID_5382324,Human_RBP_ID_19103263,Human_RBP_ID_23212207 Human_Splice_Rec_377530,Human_Splice_Rec_377531,Human_Splice_Rec_377558,Human_Splice_Rec_377559,Human_Splice_Rec_377578,Human_Splice_Rec_377579,Human_Splice_Rec_377592,Human_Splice_Rec_377593,Human_Splice_Rec_377610,Human_Splice_Rec_377611,Human_Splice_Rec_377638,Human_Splice_Rec_377639,Human_Splice_Rec_377656,Human_Splice_Rec_377657,Human_Splice_Rec_377664 RMVar_hsa_circ_12827,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_344547,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_312803,RMVar_hsa_circ_291146,RMVar_hsa_circ_295847,RMVar_hsa_circ_207941,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_207947,RMVar_hsa_circ_267376,RMVar_hsa_circ_38258,RMVar_hsa_circ_47016,RMVar_hsa_circ_266227 62346 RMVar_ID_62346 Human_SNP_ID_118914680 m1A Human chr2 - 240018558 240018558 240018558 GGAGGCGATGTACAACCAGGGATTCATCCGAAAGCAGTGTGAGTCAGCATTGCAGACCCACTTCT GGAGGCGATGTACAACCAGGGATTCATCCGAAGGCAGTGTGAGTCAGCATTGCAGACCCACTTCT T C NDUFA10 Ensembl:ENSG00000130414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:240018551..240018650 32194978 MeRIP-seq:(Medium) rs1012086424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546720,Human_RBP_ID_922445,Human_RBP_ID_3959970,Human_RBP_ID_5382324,Human_RBP_ID_19103263,Human_RBP_ID_23212207 Human_Splice_Rec_377530,Human_Splice_Rec_377531,Human_Splice_Rec_377558,Human_Splice_Rec_377559,Human_Splice_Rec_377578,Human_Splice_Rec_377579,Human_Splice_Rec_377592,Human_Splice_Rec_377593,Human_Splice_Rec_377610,Human_Splice_Rec_377611,Human_Splice_Rec_377638,Human_Splice_Rec_377639,Human_Splice_Rec_377656,Human_Splice_Rec_377657,Human_Splice_Rec_377664 RMVar_hsa_circ_12827,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_344547,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_312803,RMVar_hsa_circ_291146,RMVar_hsa_circ_295847,RMVar_hsa_circ_207941,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_207947,RMVar_hsa_circ_267376,RMVar_hsa_circ_38258,RMVar_hsa_circ_47016,RMVar_hsa_circ_266227 62347 RMVar_ID_62347 Human_SNP_ID_118915773 m1A Human chr2 - 240022340 240022329 240022341 AATGTGCTGCTGTGTGATTTTGTGTTTTTCAGAGAGGAATTCATAGCAGTGTGCAGTGCAAACTG AATGTGCTGCTGTGTGATTTTGTGTTTTTCA____________TAGCAGTGTGCAGTGCAAACTG ATGAATTCCTCTC A NDUFA10 Ensembl:ENSG00000130414 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:240022290..240022389 26863196 MeRIP-seq:(Medium) rs751255623 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_4601344,Human_RBP_ID_27819460 Human_Splice_Rec_377526,Human_Splice_Rec_377554,Human_Splice_Rec_377574,Human_Splice_Rec_377606,Human_Splice_Rec_377634,Human_Splice_Rec_377660,Human_Splice_Rec_377666 RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_274735,RMVar_hsa_circ_207939,RMVar_hsa_circ_291146,RMVar_hsa_circ_351589,RMVar_hsa_circ_207940,RMVar_hsa_circ_207947,RMVar_hsa_circ_267376,RMVar_hsa_circ_38258,RMVar_hsa_circ_47016,RMVar_hsa_circ_111279,RMVar_hsa_circ_266227,RMVar_hsa_circ_207951 62348 RMVar_ID_62348 Human_SNP_ID_118915776 m1A Human chr2 - 240022342 240022342 240022342 ACAATGTGCTGCTGTGTGATTTTGTGTTTTTCAGAGAGGAATTCATAGCAGTGTGCAGTGCAAAC ACAATGTGCTGCTGTGTGATTTTGTGTTTTTCGGAGAGGAATTCATAGCAGTGTGCAGTGCAAAC T C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:240022251..240022396 26863410 MeRIP-seq:(Medium) rs917371150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625675,Human_RBP_ID_27819460 62349 RMVar_ID_62349 Human_SNP_ID_118944113 m1A Human chr2 - 240131023 240131023 240131023 AGTGAGATGCCCTCTGGCTGCAGGCGGGGCCAAGCCCTTGGTACAGAGCCGCAGTGTGAGCCTGC AGTGAGATGCCCTCTGGCTGCAGGCGGGGCCAGGCCCTTGGTACAGAGCCGCAGTGTGAGCCTGC T C COPS9 Ensembl:ENSG00000172428 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240130976..240134025 26863196 MeRIP-seq:(Medium) rs200187046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546746,Human_RBP_ID_776524,Human_RBP_ID_1022531,Human_RBP_ID_1584748,Human_RBP_ID_4625235,Human_RBP_ID_5118206,Human_RBP_ID_6899975,Human_RBP_ID_17658282,Human_RBP_ID_22450972,Human_RBP_ID_23861266,Human_RBP_ID_26340494,Human_RBP_ID_27008759,Human_RBP_ID_27288090 Human_Splice_Rec_377674,Human_Splice_Rec_377680,Human_Splice_Rec_377684,Human_Splice_Rec_377688 Human_miRNA_ID_3068098 RMVar_hsa_circ_102708,RMVar_hsa_circ_207952 62350 RMVar_ID_62350 Human_SNP_ID_118944910 m1A Human chr2 - 240133993 240133993 240133993 CTTGCCTTTCCATTCCCCAGGCGGGAGGCAGCACCGGGCTCTTGATGGACTTGGCAGCCAATGAA CTTGCCTTTCCATTCCCCAGGCGGGAGGCAGCGCCGGGCTCTTGATGGACTTGGCAGCCAATGAA T C COPS9 Ensembl:ENSG00000172428 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:240131003..240134069;chr2:240130955..240134069;chr2:240130976..240134069 26863196 MeRIP-seq:(Medium) rs1449696051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546755,Human_RBP_ID_776525,Human_RBP_ID_4623926,Human_RBP_ID_13817903,Human_RBP_ID_17658283,Human_RBP_ID_19099021,Human_RBP_ID_22452024,Human_RBP_ID_22547969,Human_RBP_ID_25524387 Human_Splice_Rec_377672,Human_Splice_Rec_377673,Human_Splice_Rec_377679,Human_Splice_Rec_377682,Human_Splice_Rec_377683,Human_Splice_Rec_377686,Human_Splice_Rec_377687,Human_Splice_Rec_377690 RMVar_hsa_circ_102708,RMVar_hsa_circ_207952 62351 RMVar_ID_62351 Human_SNP_ID_118944911 m1A Human chr2 - 240134000 240134000 240134000 ACATAACCTTGCCTTTCCATTCCCCAGGCGGGAGGCAGCACCGGGCTCTTGATGGACTTGGCAGC ACATAACCTTGCCTTTCCATTCCCCAGGCGGGGGGCAGCACCGGGCTCTTGATGGACTTGGCAGC T C COPS9 Ensembl:ENSG00000172428 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:240133926..240134072 26863410 MeRIP-seq:(Medium) rs778032765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546755,Human_RBP_ID_776525,Human_RBP_ID_4601370,Human_RBP_ID_13817903,Human_RBP_ID_17658283,Human_RBP_ID_19099021,Human_RBP_ID_22452024,Human_RBP_ID_22547969 Human_Splice_Rec_377672,Human_Splice_Rec_377673,Human_Splice_Rec_377679,Human_Splice_Rec_377682,Human_Splice_Rec_377683,Human_Splice_Rec_377686,Human_Splice_Rec_377687,Human_Splice_Rec_377690 RMVar_hsa_circ_102708,RMVar_hsa_circ_207952 62352 RMVar_ID_62352 Human_SNP_ID_118945584 m1A Human chr2 - 240136253 240136253 240136253 GATGAAGCCGGCGGTGGACGAGATGTTCCCCGAGGGCGCCGGGCCCTACGTGGACCTGGACGAGG GATGAAGCCGGCGGTGGACGAGATGTTCCCCGTGGGCGCCGGGCCCTACGTGGACCTGGACGAGG T A COPS9 Ensembl:ENSG00000172428 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:240136226..240136300 26863196 MeRIP-seq:(Medium) rs1250644125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61715,Human_RBP_ID_546756,Human_RBP_ID_4601375,Human_RBP_ID_5322337,Human_RBP_ID_17658773,Human_RBP_ID_22450973,Human_RBP_ID_23861284 Human_Splice_Rec_377671,Human_Splice_Rec_377685,Human_Splice_Rec_377689 62353 RMVar_ID_62353 Human_SNP_ID_119014888 m1A Human chr2 + 240383997 240383997 240383997 GGACACGTCGCCCACCACTGCCCTCGGTCACCACTGGACCCGACACCCACCACTGCCCTCGGTCA GGACACGTCGCCCACCACTGCCCTCGGTCACCGCTGGACCCGACACCCACCACTGCCCTCGGTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240383874..240384042 26863196 MeRIP-seq:(Medium) rs534113230 Functional Loss SNV dbSNP153 33..33 33 - - - 62354 RMVar_ID_62354 Human_SNP_ID_119026568 m1A Human chr2 + 240426981 240426973 240426982 CTCTTAAACAACCAGCTTTCTCGTGTGAACTAACTCAGCGACAGCTCACTCATCGCCAAGGGGAT CTCTTAAACAACCAGCTTTCTCGTG_________TCAGCGACAGCTCACTCATCGCCAAGGGGAT GTGAACTAAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240426940..240427062 26863196 MeRIP-seq:(Medium) rs1559188980 Functional Loss DEL dbSNP153 26..34 33 - - - 62355 RMVar_ID_62355 Human_SNP_ID_119026575 m1A Human chr2 + 240426981 240426981 240426981 CTCTTAAACAACCAGCTTTCTCGTGTGAACTAACTCAGCGACAGCTCACTCATCGCCAAGGGGAT CTCTTAAACAACCAGCTTTCTCGTGTGAACTATCTCAGCGACAGCTCACTCATCGCCAAGGGGAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240426940..240427062 26863196 MeRIP-seq:(Medium) rs1454218218 Functional Loss SNV dbSNP153 33..33 33 - - - 62356 RMVar_ID_62356 Human_SNP_ID_119029199 m1A Human chr2 + 240435727 240435727 240435727 CTGGGCTGCCCGAGCGAGCGTTCGGACCTCGCACCCCGCGCGCCCCGCGCCGCCGCCGCCGCCGG CTGGGCTGCCCGAGCGAGCGTTCGGACCTCGCGCCCCGCGCGCCCCGCGCCGCCGCCGCCGCCGG A G GPC1 Ensembl:ENSG00000063660 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240435678..240435805 26863196 MeRIP-seq:(Medium) rs1290754318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625239 RMVar_hsa_circ_80045,RMVar_hsa_circ_207953 62357 RMVar_ID_62357 Human_SNP_ID_119029279 m1A Human chr2 - 240435947 240435944 240435947 CGCAGGCGACCAGCGCTGCGGCCGCACATAGCAGCCACCAGCCTCGGGCCCGGAGCTCCATGGCG CGCAGGCGACCAGCGCTGCGGCCGCACATAGC___CACCAGCCTCGGGCCCGGAGCTCCATGGCG GGCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240435897..240436014 26863196 MeRIP-seq:(Medium) rs1470947612 Functional Loss DEL dbSNP153 33..35 33 - - - 62358 RMVar_ID_62358 Human_SNP_ID_119033824 m1A Human chr2 + 240450941 240450941 240450941 GCTGGGGAGGCTTCCTGAGGGAGGTGAGGGGAAAGCATGTGAGATGGAGGGAAGTGGCAGGTCAC GCTGGGGAGGCTTCCTGAGGGAGGTGAGGGGAGAGCATGTGAGATGGAGGGAAGTGGCAGGTCAC A G GPC1 Ensembl:ENSG00000063660 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:240450856..240450985 26863196 MeRIP-seq:(Medium) rs118190533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80045,RMVar_hsa_circ_207953 62359 RMVar_ID_62359 Human_SNP_ID_119034496 m1A Human chr2 + 240452853 240452853 240452853 CGGCTGCGGCGCTGCCCGGGGTGGCTGCGGCCAGAGTCTCCCGCGCGCCCGGCGGACCGCAGCCC CGGCTGCGGCGCTGCCCGGGGTGGCTGCGGCCGGAGTCTCCCGCGCGCCCGGCGGACCGCAGCCC A G GPC1 Ensembl:ENSG00000063660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240452847..240453157 26863196 MeRIP-seq:(Medium) rs938964035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80045,RMVar_hsa_circ_207953 62360 RMVar_ID_62360 Human_SNP_ID_119035334 m1A Human chr2 + 240454397 240454397 240454397 GGCTGCTGGACGTGCCGGAGGATGCCACAGCCACCGGAGCTGGTTGGGGTCCGAGAGCAGATGGG GGCTGCTGGACGTGCCGGAGGATGCCACAGCCGCCGGAGCTGGTTGGGGTCCGAGAGCAGATGGG A G GPC1 Ensembl:ENSG00000063660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240454393..240454548 26863196 MeRIP-seq:(Medium) rs1297619236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80045,RMVar_hsa_circ_207953 62361 RMVar_ID_62361 Human_SNP_ID_119035624 m1A Human chr2 + 240455265 240455265 240455265 ATCCCCTTCCCCCCCAAAAAAATCCTCAGAGCACTGGGGAAGGGAAGTGTCCCAGTGACTGAGGG ATCCCCTTCCCCCCCAAAAAAATCCTCAGAGCCCTGGGGAAGGGAAGTGTCCCAGTGACTGAGGG A C GPC1 Ensembl:ENSG00000063660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240455261..240455415 26863196 MeRIP-seq:(Medium) rs971107048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80045,RMVar_hsa_circ_207953 62362 RMVar_ID_62362 Human_SNP_ID_119039649 m1A Human chr2 + 240465598 240465598 240465598 GCAGCAGATCATGCAGCTGAAGATCATGACCAACCGGCTGCGCAGCGCCTACAACGGCAACGACG GCAGCAGATCATGCAGCTGAAGATCATGACCACCCGGCTGCGCAGCGCCTACAACGGCAACGACG A C GPC1 Ensembl:ENSG00000063660 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240465550..240465662 26863196 MeRIP-seq:(Medium) rs940548615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56233 Human_Splice_Rec_377729,Human_Splice_Rec_377743,Human_Splice_Rec_377757,Human_Splice_Rec_377787,Human_Splice_Rec_377797,Human_Splice_Rec_377799 RMVar_hsa_circ_13927,RMVar_hsa_circ_80045,RMVar_hsa_circ_81970,RMVar_hsa_circ_207953,RMVar_hsa_circ_207955,RMVar_hsa_circ_207954,RMVar_hsa_circ_101314,RMVar_hsa_circ_80551,RMVar_hsa_circ_91872,RMVar_hsa_circ_207958,RMVar_hsa_circ_207959,RMVar_hsa_circ_97619,RMVar_hsa_circ_207960,RMVar_hsa_circ_91453,RMVar_hsa_circ_207961,RMVar_hsa_circ_207962 62363 RMVar_ID_62363 Human_SNP_ID_119039901 m1A Human chr2 + 240466126 240466126 240466126 GTCTGGATGACCTCTGCAGCCGGAAGGTCAGCAGGAAGAGCTCCAGCTCCCGGACGCCCTTGACC GTCTGGATGACCTCTGCAGCCGGAAGGTCAGCGGGAAGAGCTCCAGCTCCCGGACGCCCTTGACC A G GPC1 Ensembl:ENSG00000063660 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240466076..240466307 26863196 MeRIP-seq:(Medium) rs777765903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22766330 Human_Splice_Rec_377730,Human_Splice_Rec_377744,Human_Splice_Rec_377758,Human_Splice_Rec_377788,Human_Splice_Rec_377798,Human_Splice_Rec_377800 RMVar_hsa_circ_80045,RMVar_hsa_circ_81970,RMVar_hsa_circ_207953,RMVar_hsa_circ_207955,RMVar_hsa_circ_101314,RMVar_hsa_circ_82031,RMVar_hsa_circ_80551,RMVar_hsa_circ_91872,RMVar_hsa_circ_207958,RMVar_hsa_circ_207959,RMVar_hsa_circ_97619,RMVar_hsa_circ_207960,RMVar_hsa_circ_91453,RMVar_hsa_circ_207961,RMVar_hsa_circ_207962,RMVar_hsa_circ_207963 62364 RMVar_ID_62364 Human_SNP_ID_119039913 m1A Human chr2 - 240466161 240466161 240466161 TGTCCTTCCTGCTCTGACAGGCCTGGGAGGGCATGGGTCAAGGGCGTCCGGGAGCTGGAGCTCTT TGTCCTTCCTGCTCTGACAGGCCTGGGAGGGCCTGGGTCAAGGGCGTCCGGGAGCTGGAGCTCTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240466111..240466277 26863196 MeRIP-seq:(Medium) rs772413143 Functional Loss SNV dbSNP153 33..33 33 - - - 62365 RMVar_ID_62365 Human_SNP_ID_119039920 m1A Human chr2 + 240466196 240466196 240466196 CCTCCCAGGCCTGTCAGAGCAGGAAGGACAGAAGACCTCGGCTGCCAGCTGCCCCCAGCCCCCGA CCTCCCAGGCCTGTCAGAGCAGGAAGGACAGACGACCTCGGCTGCCAGCTGCCCCCAGCCCCCGA A C GPC1 Ensembl:ENSG00000063660 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240466051..240466270 26863196 MeRIP-seq:(Medium) rs137923533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22450975,Human_RBP_ID_22766330,Human_RBP_ID_26480874 Human_miRNA_ID_1358969 RMVar_hsa_circ_80045,RMVar_hsa_circ_81970,RMVar_hsa_circ_207953,RMVar_hsa_circ_207955,RMVar_hsa_circ_101314,RMVar_hsa_circ_82031,RMVar_hsa_circ_80551,RMVar_hsa_circ_91872,RMVar_hsa_circ_207958,RMVar_hsa_circ_207959,RMVar_hsa_circ_97619,RMVar_hsa_circ_207960,RMVar_hsa_circ_91453,RMVar_hsa_circ_207961,RMVar_hsa_circ_207962,RMVar_hsa_circ_207963 62366 RMVar_ID_62366 Human_SNP_ID_119040430 m1A Human chr2 - 240467729 240467729 240467729 AACATCTAAAGTCAGGTTCCAGAGAACAAGCCATGGGGACCTGACCAGCAACCGGGGACCTCCGT AACATCTAAAGTCAGGTTCCAGAGAACAAGCCGTGGGGACCTGACCAGCAACCGGGGACCTCCGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240467679..240468028 32194978 MeRIP-seq:(Medium) rs1341363848 Functional Loss SNV dbSNP153 33..33 33 - - - 62367 RMVar_ID_62367 Human_SNP_ID_119051039 m1A Human chr2 - 240509862 240509862 240509862 TCCACCAGCCGAGGGTGGGGCTCTTTACACTCAGGCCGTCCTCTACGATCACTGAGCCCTGGTGG TCCACCAGCCGAGGGTGGGGCTCTTTACACTCGGGCCGTCCTCTACGATCACTGAGCCCTGGTGG T C ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240509815..240510135 26863196 MeRIP-seq:(Medium) rs560566623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3640368,Human_RBP_ID_9429459 RMVar_hsa_circ_207965,RMVar_hsa_circ_92801,RMVar_hsa_circ_330191,RMVar_hsa_circ_337796,RMVar_hsa_circ_372717,RMVar_hsa_circ_291750,RMVar_hsa_circ_207966,RMVar_hsa_circ_69758,RMVar_hsa_circ_341953,RMVar_hsa_circ_347733,RMVar_hsa_circ_207964,RMVar_hsa_circ_342395,RMVar_hsa_circ_53903,RMVar_hsa_circ_36644,RMVar_hsa_circ_207969,RMVar_hsa_circ_59311,RMVar_hsa_circ_372871,RMVar_hsa_circ_366073 62368 RMVar_ID_62368 Human_SNP_ID_119054666 m1A Human chr2 - 240522199 240522199 240522199 TGTCTAGCTAAAGGATTGTAAATGCACCAATCAATGCTCAGTGTCTAGCTAAAGGATTGTAAATG TGTCTAGCTAAAGGATTGTAAATGCACCAATCGATGCTCAGTGTCTAGCTAAAGGATTGTAAATG T C ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:240522152..240522242 26863410 MeRIP-seq:(Medium) rs939094410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207965,RMVar_hsa_circ_92801,RMVar_hsa_circ_330191,RMVar_hsa_circ_337796,RMVar_hsa_circ_341953,RMVar_hsa_circ_347733,RMVar_hsa_circ_207964,RMVar_hsa_circ_53903,RMVar_hsa_circ_93116,RMVar_hsa_circ_36644,RMVar_hsa_circ_59311,RMVar_hsa_circ_366073,RMVar_hsa_circ_29790,RMVar_hsa_circ_373861,RMVar_hsa_circ_207970,RMVar_hsa_circ_107477,RMVar_hsa_circ_207971,RMVar_hsa_circ_207972 62369 RMVar_ID_62369 Human_SNP_ID_119054667 m1A Human chr2 - 240522199 240522199 240522199 TGTCTAGCTAAAGGATTGTAAATGCACCAATCAATGCTCAGTGTCTAGCTAAAGGATTGTAAATG TGTCTAGCTAAAGGATTGTAAATGCACCAATCCATGCTCAGTGTCTAGCTAAAGGATTGTAAATG T G ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:240522152..240522242 26863410 MeRIP-seq:(Medium) rs939094410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207965,RMVar_hsa_circ_92801,RMVar_hsa_circ_330191,RMVar_hsa_circ_337796,RMVar_hsa_circ_341953,RMVar_hsa_circ_347733,RMVar_hsa_circ_207964,RMVar_hsa_circ_53903,RMVar_hsa_circ_93116,RMVar_hsa_circ_36644,RMVar_hsa_circ_59311,RMVar_hsa_circ_366073,RMVar_hsa_circ_29790,RMVar_hsa_circ_373861,RMVar_hsa_circ_207970,RMVar_hsa_circ_107477,RMVar_hsa_circ_207971,RMVar_hsa_circ_207972 62370 RMVar_ID_62370 Human_SNP_ID_119055245 m1A Human chr2 - 240524178 240524178 240524178 TTCCAGGACACCGGGCAGTGTGGGGGGTCCATAGACCACAGGAGCAGCTCTCTGAAGGGGGACTC TTCCAGGACACCGGGCAGTGTGGGGGGTCCATGGACCACAGGAGCAGCTCTCTGAAGGGGGACTC T C ANKMY1 Ensembl:ENSG00000144504 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35996697 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7636 RMVar_hsa_circ_207965,RMVar_hsa_circ_92801,RMVar_hsa_circ_330191,RMVar_hsa_circ_337796,RMVar_hsa_circ_4972,RMVar_hsa_circ_341953,RMVar_hsa_circ_347733,RMVar_hsa_circ_207964,RMVar_hsa_circ_53903,RMVar_hsa_circ_93116,RMVar_hsa_circ_36644,RMVar_hsa_circ_59311,RMVar_hsa_circ_366073,RMVar_hsa_circ_29790,RMVar_hsa_circ_373861,RMVar_hsa_circ_207970,RMVar_hsa_circ_107477,RMVar_hsa_circ_207971,RMVar_hsa_circ_316676,RMVar_hsa_circ_368315,RMVar_hsa_circ_207972,RMVar_hsa_circ_323613,RMVar_hsa_circ_303441,RMVar_hsa_circ_207973,RMVar_hsa_circ_207974 62371 RMVar_ID_62371 Human_SNP_ID_119063742 m1A Human chr2 - 240554927 240554926 240554927 TGTGCAGGAGTGGCAGGATGGTTGCATGTACCAGGGGGAGTTTGGGTTGAACATGAAGCTTGGAT TGTGCAGGAGTGGCAGGATGGTTGCATGTACC_GGGGGAGTTTGGGTTGAACATGAAGCTTGGAT CT C ANKMY1 Ensembl:ENSG00000144504 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240554878..240555009 26863196 MeRIP-seq:(Medium) rs1311408445 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_776176,Human_RBP_ID_9385804,Human_RBP_ID_22249305 Human_Splice_Rec_377813,Human_Splice_Rec_377839,Human_Splice_Rec_377869,Human_Splice_Rec_377903,Human_Splice_Rec_377929,Human_Splice_Rec_377961,Human_Splice_Rec_377989,Human_Splice_Rec_378035,Human_Splice_Rec_378047,Human_Splice_Rec_378065,Human_Splice_Rec_378075,Human_Splice_Rec_378085,Human_Splice_Rec_378091,Human_Splice_Rec_378097,Human_Splice_Rec_378103,Human_Splice_Rec_378107 RMVar_hsa_circ_330191,RMVar_hsa_circ_341953,RMVar_hsa_circ_36644,RMVar_hsa_circ_59311,RMVar_hsa_circ_373861,RMVar_hsa_circ_207970,RMVar_hsa_circ_323613,RMVar_hsa_circ_39177,RMVar_hsa_circ_353483,RMVar_hsa_circ_207975,RMVar_hsa_circ_281015,RMVar_hsa_circ_207977 62372 RMVar_ID_62372 Human_SNP_ID_119065770 m1A Human chr2 - 240560962 240560962 240560962 TGCAGTAGACTAGGCAGGCGCCGCCGGCGCGCACCGCGGCCTCCATGGCGGCGCACGTGGGCTCC TGCAGTAGACTAGGCAGGCGCCGCCGGCGCGCCCCGCGGCCTCCATGGCGGCGCACGTGGGCTCC T G ANKMY1 Ensembl:ENSG00000144504 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240560916..240561003 26863196 MeRIP-seq:(Medium) rs960942830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422058 62373 RMVar_ID_62373 Human_SNP_ID_119068141 m1A Human chr2 + 240568303 240568283 240568303 TCACCCGCTCCGCGCGCCTCGGCTCCCAACACAGCGCCCCGGCCCCGCGCCGCGCTCGATTCCCC TCACCCGCTCCGC____________________GCGCCCCGGCCCCGCGCCGCGCTCGATTCCCC CGCGCCTCGGCTCCCAACACA C RNPEPL1 Ensembl:ENSG00000142327 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240568258..240568331 26863196 MeRIP-seq:(Medium) rs975032506 Functional Loss DEL dbSNP153 14..33 33 - - - 62374 RMVar_ID_62374 Human_SNP_ID_119068361 m1A Human chr2 - 240568845 240568845 240568845 GGCGGCGGCGGGGGCGCGACGGAAGGCGGCTGAGTGCAGGCGCAGAGCCGGGTGCGCGTCGAGCA GGCGGCGGCGGGGGCGCGACGGAAGGCGGCTGGGTGCAGGCGCAGAGCCGGGTGCGCGTCGAGCA T C ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240568747..240568897 32194978 MeRIP-seq:(Medium) rs1285808370 Functional Loss SNV dbSNP153 33..33 33 - - - 62375 RMVar_ID_62375 Human_SNP_ID_119068405 m1A Human chr2 - 240568905 240568905 240568905 GGGCGGCGGCGCGGGCCCCGGCCCGGGGGCGGAGAAGGCGAAGGCGCAGGGCGTCTCGGCGGCGG GGGCGGCGGCGCGGGCCCCGGCCCGGGGGCGGTGAAGGCGAAGGCGCAGGGCGTCTCGGCGGCGG T A ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240568883..240569036 26863196 MeRIP-seq:(Medium) rs1158328998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26787517 62376 RMVar_ID_62376 Human_SNP_ID_119069786 m1A Human chr2 + 240573154 240573154 240573154 GTGCAGGTGCTGATGAGTGCCACCCGGAGTGCATACATGGAGGAAGAAGGCGTCTTCCACTTCCA GTGCAGGTGCTGATGAGTGCCACCCGGAGTGCGTACATGGAGGAAGAAGGCGTCTTCCACTTCCA A G RNPEPL1 Ensembl:ENSG00000142327 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240568976..240573911 32194978 MeRIP-seq:(Medium) rs756571696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22668266,Human_RBP_ID_24376774 Human_Splice_Rec_378134,Human_Splice_Rec_378154 Human_miRNA_ID_3012068 RMVar_hsa_circ_59991,RMVar_hsa_circ_83829,RMVar_hsa_circ_207978,RMVar_hsa_circ_41354 62377 RMVar_ID_62377 Human_SNP_ID_119071171 m1A Human chr2 - 240576959 240576959 240576959 CCTGGCTCTCCAGGAAGCGCCGCACCCTGTGGAGGTCAGGATAGTAGTCGTTGCGGACCACAATC CCTGGCTCTCCAGGAAGCGCCGCACCCTGTGGGGGTCAGGATAGTAGTCGTTGCGGACCACAATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240576826..240578036 32194978 MeRIP-seq:(Medium) rs1193862241 Functional Loss SNV dbSNP153 33..33 33 - - - 62378 RMVar_ID_62378 Human_SNP_ID_119074120 m1A Human chr2 + 240586874 240586874 240586874 TGACTCGCCTTCTCTCCGGGGCTGCGACCCCGAGGCAACCGGCTGCAGATGGGAGCCCGCGGAGC TGACTCGCCTTCTCTCCGGGGCTGCGACCCCGTGGCAACCGGCTGCAGATGGGAGCCCGCGGAGC A T CAPN10 Ensembl:ENSG00000142330 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:240586776..240586975 26863196 MeRIP-seq:(Medium) rs1215404495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5380356,Human_RBP_ID_17953556,Human_RBP_ID_18422566,Human_RBP_ID_19000980 62379 RMVar_ID_62379 Human_SNP_ID_119074132 m1A Human chr2 + 240586912 240586912 240586912 CCGGCTGCAGATGGGAGCCCGCGGAGCCGAGGATGCGGGCGGGCCGGGGCGCGACGCCGGCGAGG CCGGCTGCAGATGGGAGCCCGCGGAGCCGAGGGTGCGGGCGGGCCGGGGCGCGACGCCGGCGAGG A G CAPN10 Ensembl:ENSG00000142330 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240586756..240587009 26863196 MeRIP-seq:(Medium) rs1429597641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4601594 62380 RMVar_ID_62380 Human_SNP_ID_119075682 m1A Human chr2 + 240592062 240592062 240592062 GTAGCAGGAAGCGGAGGCCAGCAGGACAGGCCAGGCCGCTGGGAGCACAGGACTTGTCGGCAGCT GTAGCAGGAAGCGGAGGCCAGCAGGACAGGCCGGGCCGCTGGGAGCACAGGACTTGTCGGCAGCT A G CAPN10 Ensembl:ENSG00000142330 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240592017..240592118 26863196 MeRIP-seq:(Medium) rs3792269 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_242891,Human_RBP_ID_19003475 Human_Splice_Rec_378213,Human_Splice_Rec_378233,Human_Splice_Rec_378263,Human_Splice_Rec_378283,Human_Splice_Rec_378305,Human_Splice_Rec_378323,Human_Splice_Rec_378343,Human_Splice_Rec_378357,Human_Splice_Rec_378373 Clinvar_Rec_228 GWAS_ID_7637,GWAS_ID_7638,GWAS_ID_7639,GWAS_ID_7640,GWAS_ID_7641,GWAS_ID_7642,GWAS_ID_7643,GWAS_ID_7644,GWAS_ID_7645,GWAS_ID_7646,GWAS_ID_7647,GWAS_ID_7648,GWAS_ID_7649,GWAS_ID_7650,GWAS_ID_7651,GWAS_ID_7652,GWAS_ID_7653,GWAS_ID_7654,GWAS_ID_7655,GWAS_ID_7656,GWAS_ID_7657,GWAS_ID_7658,GWAS_ID_7659,GWAS_ID_7660,GWAS_ID_7661,GWAS_ID_7662,GWAS_ID_7663,GWAS_ID_7664,GWAS_ID_7665,GWAS_ID_7666 RMVar_hsa_circ_4606,RMVar_hsa_circ_340379,RMVar_hsa_circ_103084,RMVar_hsa_circ_207984 62381 RMVar_ID_62381 Human_SNP_ID_119076280 m1A Human chr2 + 240593969 240593969 240593969 CATTGTCTCGGACCTGCGGGAGCTCCAGGGTCAGGCGGGCCAGTGCATCCTGCTGCTGCGGATCC CATTGTCTCGGACCTGCGGGAGCTCCAGGGTCCGGCGGGCCAGTGCATCCTGCTGCTGCGGATCC A C CAPN10 Ensembl:ENSG00000142330 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240593920..240594264 32194978 MeRIP-seq:(Medium) rs548715768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242892,Human_RBP_ID_919607,Human_RBP_ID_9388305,Human_RBP_ID_19000983 Human_Splice_Rec_378214,Human_Splice_Rec_378215,Human_Splice_Rec_378234,Human_Splice_Rec_378235,Human_Splice_Rec_378264,Human_Splice_Rec_378265,Human_Splice_Rec_378284,Human_Splice_Rec_378285,Human_Splice_Rec_378306,Human_Splice_Rec_378307,Human_Splice_Rec_378324,Human_Splice_Rec_378325,Human_Splice_Rec_378344,Human_Splice_Rec_378345,Human_Splice_Rec_378358,Human_Splice_Rec_378359 RMVar_hsa_circ_103084,RMVar_hsa_circ_207984 62382 RMVar_ID_62382 Human_SNP_ID_119076281 m1A Human chr2 + 240593969 240593969 240593969 CATTGTCTCGGACCTGCGGGAGCTCCAGGGTCAGGCGGGCCAGTGCATCCTGCTGCTGCGGATCC CATTGTCTCGGACCTGCGGGAGCTCCAGGGTCGGGCGGGCCAGTGCATCCTGCTGCTGCGGATCC A G CAPN10 Ensembl:ENSG00000142330 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240593920..240594264 32194978 MeRIP-seq:(Medium) rs548715768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242892,Human_RBP_ID_919607,Human_RBP_ID_9388305,Human_RBP_ID_19000983 Human_Splice_Rec_378214,Human_Splice_Rec_378215,Human_Splice_Rec_378234,Human_Splice_Rec_378235,Human_Splice_Rec_378264,Human_Splice_Rec_378265,Human_Splice_Rec_378284,Human_Splice_Rec_378285,Human_Splice_Rec_378306,Human_Splice_Rec_378307,Human_Splice_Rec_378324,Human_Splice_Rec_378325,Human_Splice_Rec_378344,Human_Splice_Rec_378345,Human_Splice_Rec_378358,Human_Splice_Rec_378359 RMVar_hsa_circ_103084,RMVar_hsa_circ_207984 62383 RMVar_ID_62383 Human_SNP_ID_119076733 m1A Human chr2 - 240595066 240595066 240595066 TGTTCCGGCAGCCTCCTGCTGACTGGCCCTTGACCCAGGCCCCAGGCAGCGCCCGCGTATGGCAG TGTTCCGGCAGCCTCCTGCTGACTGGCCCTTGGCCCAGGCCCCAGGCAGCGCCCGCGTATGGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:240594462..240596153 32194978 MeRIP-seq:(Medium) rs371277139 Functional Loss SNV dbSNP153 33..33 33 - - - 62384 RMVar_ID_62384 Human_SNP_ID_119085636 m1A Human chr2 + 240623485 240623485 240623485 TCGTGAGGGTGCAAACAGGTCGTGAGGGCGCAAACAGGTCGTGAGGGTGCAAACAGGTCGTGAGG TCGTGAGGGTGCAAACAGGTCGTGAGGGCGCAGACAGGTCGTGAGGGTGCAAACAGGTCGTGAGG A G GPR35 Ensembl:ENSG00000178623 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240623444..240623671 26863196 MeRIP-seq:(Medium) rs1305404894 Functional Loss SNV dbSNP153 33..33 33 - - - 62385 RMVar_ID_62385 Human_SNP_ID_119086377 m1A Human chr2 + 240625724 240625724 240625724 GGGGTGAGGCTGTGACGGGGGTTCTCAGAGCGAGGTGAGGCTGTGACAGGGTCTCAGAGCGGGGT GGGGTGAGGCTGTGACGGGGGTTCTCAGAGCGGGGTGAGGCTGTGACAGGGTCTCAGAGCGGGGT A G GPR35 Ensembl:ENSG00000178623 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240625654..240626133 26863196 MeRIP-seq:(Medium) rs111969030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639298,Human_RBP_ID_8201092,Human_RBP_ID_9429079,Human_RBP_ID_13819117,Human_RBP_ID_17207839,Human_RBP_ID_18422582,Human_RBP_ID_22417350,Human_RBP_ID_22700022,Human_RBP_ID_23282895,Human_RBP_ID_26787529 62386 RMVar_ID_62386 Human_SNP_ID_119192802 m1A Human chr2 + 240998745 240998745 240998745 GCGCGGCCAGCGGGCGCGCCCGCGCTCCCCGCACCCCGCCTGGCCCTGCCGGCCACCCCCGCGCG GCGCGGCCAGCGGGCGCGCCCGCGCTCCCCGCCCCCCGCCTGGCCCTGCCGGCCACCCCCGCGCG A C SNED1 Ensembl:ENSG00000162804 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240998695..240998760 26863196 MeRIP-seq:(Medium) rs1002157077 Functional Loss SNV dbSNP153 33..33 33 - - - 62387 RMVar_ID_62387 Human_SNP_ID_119219117 m1A Human chr2 + 241096067 241096052 241096067 TCCTCCGCCTCGTCGTCGTCCTCATCATCGTCATCCTCATCATTGTCATCCTCATCATTGTCCTC TCCTCCGCCTCGTCGTCG_______________TCCTCATCATTGTCATCCTCATCATTGTCCTC GTCCTCATCATCGTCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241095951..241096175 26863196 MeRIP-seq:(Medium) rs747981001 Functional Loss DEL dbSNP153 19..33 33 - - - 62388 RMVar_ID_62388 Human_SNP_ID_119219132 m1A Human chr2 + 241096067 241096067 241096067 TCCTCCGCCTCGTCGTCGTCCTCATCATCGTCATCCTCATCATTGTCATCCTCATCATTGTCCTC TCCTCCGCCTCGTCGTCGTCCTCATCATCGTCGTCCTCATCATTGTCATCCTCATCATTGTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241095951..241096175 26863196 MeRIP-seq:(Medium) rs1329441730 Functional Loss SNV dbSNP153 33..33 33 - - - 62389 RMVar_ID_62389 Human_SNP_ID_119224413 m1A Human chr2 + 241115775 241115775 241115775 TACACCAGGGGCCACCGGTCCTCAAGCATCCCATTACGCCAGGGCCACCCGGTCCCCAAGCATCC TACACCAGGGGCCACCGGTCCTCAAGCATCCCGTTACGCCAGGGCCACCCGGTCCCCAAGCATCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241115772..241115861 26863196 MeRIP-seq:(Medium) rs1257489416 Functional Loss SNV dbSNP153 33..33 33 - - - 62390 RMVar_ID_62390 Human_SNP_ID_119226393 m1A Human chr2 - 241122829 241122829 241122829 GGCTGTGGAACTGGAGGGGTTGGCGGCCTGTGAGGGCGAGTACTCCCAAAAGTACAGTACCATGA GGCTGTGGAACTGGAGGGGTTGGCGGCCTGTGGGGGCGAGTACTCCCAAAAGTACAGTACCATGA T C PASK Ensembl:ENSG00000115687 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241122734..241122907 26863196 MeRIP-seq:(Medium) rs777663495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22505354 Human_Splice_Rec_380666,Human_Splice_Rec_380667,Human_Splice_Rec_380700,Human_Splice_Rec_380701,Human_Splice_Rec_380740,Human_Splice_Rec_380741,Human_Splice_Rec_380774,Human_Splice_Rec_380775,Human_Splice_Rec_380818,Human_Splice_Rec_380819,Human_Splice_Rec_380828,Human_Splice_Rec_380829 RMVar_hsa_circ_15480,RMVar_hsa_circ_120120,RMVar_hsa_circ_269174,RMVar_hsa_circ_208027,RMVar_hsa_circ_118033,RMVar_hsa_circ_208026,RMVar_hsa_circ_208029,RMVar_hsa_circ_96990,RMVar_hsa_circ_98999,RMVar_hsa_circ_331132,RMVar_hsa_circ_208030 62391 RMVar_ID_62391 Human_SNP_ID_119226841 m1A Human chr2 + 241124109 241124109 241124109 AGCAGAACAGAGGTGTGGGGCCCTGGAGCTCCACCCGCCTCACCTCAAACTGTATACCTGAAGGG AGCAGAACAGAGGTGTGGGGCCCTGGAGCTCCCCCCGCCTCACCTCAAACTGTATACCTGAAGGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241124059..241126471 32194978 MeRIP-seq:(Medium) rs766139528 Functional Loss SNV dbSNP153 33..33 33 - - - 62392 RMVar_ID_62392 Human_SNP_ID_119228155 m1A Human chr2 - 241127728 241127728 241127728 GACGGGGGGTTTGGGGGCCCTGAGATGAAGCGAGAGCGCTGACCAAAGCATTGGCAAGTTCTCCT GACGGGGGGTTTGGGGGCCCTGAGATGAAGCGGGAGCGCTGACCAAAGCATTGGCAAGTTCTCCT T C PASK Ensembl:ENSG00000115687 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241127725..241132990 32194978 MeRIP-seq:(Medium) rs1371997625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15480,RMVar_hsa_circ_120120,RMVar_hsa_circ_269174,RMVar_hsa_circ_208027,RMVar_hsa_circ_118033,RMVar_hsa_circ_208026,RMVar_hsa_circ_208029,RMVar_hsa_circ_96990,RMVar_hsa_circ_98999,RMVar_hsa_circ_331132,RMVar_hsa_circ_208030 62393 RMVar_ID_62393 Human_SNP_ID_119232210 m1A Human chr2 + 241140581 241140581 241140581 ATGGCCTTGTTAGGGTTGCACACAGGGGCCGGAAGCAGAGGTGAGGACCACCCTGAGGACAGTCC ATGGCCTTGTTAGGGTTGCACACAGGGGCCGGCAGCAGAGGTGAGGACCACCCTGAGGACAGTCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241140000..241140766 32194978 MeRIP-seq:(Medium) rs761530107 Functional Loss SNV dbSNP153 33..33 33 - - - 62394 RMVar_ID_62394 Human_SNP_ID_119235248 m1A Human chr2 - 241150542 241150542 241150542 GGGCCGCCGCCCGCAGGGGCCGCTCACCCTCCATCATCTCCTGCGACTGTTGCTGCCCCGCGCCG GGGCCGCCGCCCGCAGGGGCCGCTCACCCTCCTTCATCTCCTGCGACTGTTGCTGCCCCGCGCCG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:241150476..241150602 26863410 MeRIP-seq:(Medium) rs1024748224 Functional Loss SNV dbSNP153 33..33 33 - - - 62395 RMVar_ID_62395 Human_SNP_ID_119235249 m1A Human chr2 - 241150542 241150542 241150542 GGGCCGCCGCCCGCAGGGGCCGCTCACCCTCCATCATCTCCTGCGACTGTTGCTGCCCCGCGCCG GGGCCGCCGCCCGCAGGGGCCGCTCACCCTCCGTCATCTCCTGCGACTGTTGCTGCCCCGCGCCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:241150476..241150602 26863410 MeRIP-seq:(Medium) rs1024748224 Functional Loss SNV dbSNP153 33..33 33 - - - 62396 RMVar_ID_62396 Human_SNP_ID_119236043 m1A Human chr2 - 241153397 241153397 241153397 TTTGAGGAACATATAATAAACACCCGGTTGTAAGTCAAAAGGATTTCATTTAAACATGTTTGTTG TTTGAGGAACATATAATAAACACCCGGTTGTAGGTCAAAAGGATTTCATTTAAACATGTTTGTTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241153390..241153625 26863196 MeRIP-seq:(Medium) rs1204190331 Functional Loss SNV dbSNP153 33..33 33 - - - 62397 RMVar_ID_62397 Human_SNP_ID_119236048 m1A Human chr2 - 241153415 241153411 241153416 ACATCCACTTTATGGGACTTTGAGGAACATATAATAAACACCCGGTTGTAAGTCAAAAGGATTTC ACATCCACTTTATGGGACTTTGAGGAACATA_____AACACCCGGTTGTAAGTCAAAAGGATTTC TTATTA T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:241153413..241153625 26863196 MeRIP-seq:(Medium) rs762952342 Functional Loss DEL dbSNP153 32..36 33 - - - 62398 RMVar_ID_62398 Human_SNP_ID_119239828 m1A Human chr2 + 241167118 241167118 241167118 GAGCCCCCACCCTCCTCAGCTGCCTCCAGCTCACCCTGCTCTGCCCCAGTGCGGTGTTCAAGACA GAGCCCCCACCCTCCTCAGCTGCCTCCAGCTCGCCCTGCTCTGCCCCAGTGCGGTGTTCAAGACA A G PPP1R7 Ensembl:ENSG00000115685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241166821..241167175 26863196 MeRIP-seq:(Medium) rs780043005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546937 Human_Splice_Rec_380896,Human_Splice_Rec_380964,Human_Splice_Rec_381014,Human_Splice_Rec_381038 RMVar_hsa_circ_113787,RMVar_hsa_circ_123887,RMVar_hsa_circ_208038,RMVar_hsa_circ_351866,RMVar_hsa_circ_81086,RMVar_hsa_circ_208039,RMVar_hsa_circ_208040,RMVar_hsa_circ_309287,RMVar_hsa_circ_208042,RMVar_hsa_circ_113099,RMVar_hsa_circ_92793,RMVar_hsa_circ_208043,RMVar_hsa_circ_208045,RMVar_hsa_circ_318546,RMVar_hsa_circ_91633,RMVar_hsa_circ_89441,RMVar_hsa_circ_91476,RMVar_hsa_circ_208046,RMVar_hsa_circ_120735,RMVar_hsa_circ_208049,RMVar_hsa_circ_57663,RMVar_hsa_circ_208048,RMVar_hsa_circ_99815,RMVar_hsa_circ_208050,RMVar_hsa_circ_208051 62399 RMVar_ID_62399 Human_SNP_ID_119255183 m1A Human chr2 + 241218380 241218380 241218380 CCTCCTTCGCCGCCGCGCACAACCGCACGTGCAGGTGAGCCCCGCGCCAGGTGGAGGGGGCCGCG CCTCCTTCGCCGCCGCGCACAACCGCACGTGCCGGTGAGCCCCGCGCCAGGTGGAGGGGGCCGCG A C ANO7 Ensembl:ENSG00000146205 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241218335..241218426 26863196 MeRIP-seq:(Medium) rs1354078452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920326,Human_RBP_ID_19103315 Human_Splice_Rec_381139,Human_Splice_Rec_381185,Human_Splice_Rec_381231,Human_Splice_Rec_381245,Human_Splice_Rec_381249,Human_Splice_Rec_381251,Human_Splice_Rec_381255 RMVar_hsa_circ_85061,RMVar_hsa_circ_208053 62400 RMVar_ID_62400 Human_SNP_ID_119255268 m1A Human chr2 - 241218551 241218551 241218551 GCCCCGCAAAGCTCCGTCCCTTACCGCGGGGAACCTCCCCCCAGCCCCTGCCCACGGCGCCCCCA GCCCCGCAAAGCTCCGTCCCTTACCGCGGGGAGCCTCCCCCCAGCCCCTGCCCACGGCGCCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241218548..241218662 26863196 MeRIP-seq:(Medium) rs1036148452 Functional Loss SNV dbSNP153 33..33 33 - - - 62401 RMVar_ID_62401 Human_SNP_ID_119255269 m1A Human chr2 - 241218551 241218551 241218551 GCCCCGCAAAGCTCCGTCCCTTACCGCGGGGAACCTCCCCCCAGCCCCTGCCCACGGCGCCCCCA GCCCCGCAAAGCTCCGTCCCTTACCGCGGGGACCCTCCCCCCAGCCCCTGCCCACGGCGCCCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241218548..241218662 26863196 MeRIP-seq:(Medium) rs1036148452 Functional Loss SNV dbSNP153 33..33 33 - - - 62402 RMVar_ID_62402 Human_SNP_ID_119258704 m1A Human chr2 - 241229331 241229331 241229331 GTGCTAAGATAACAGACTCCAGCTCCTGGTCCACCCGGCATGTCAGTCAGCACTCTGGCCTTCAT GTGCTAAGATAACAGACTCCAGCTCCTGGTCCCCCCGGCATGTCAGTCAGCACTCTGGCCTTCAT T G HDLBP Ensembl:ENSG00000115677 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241229176..241229469 26863196 MeRIP-seq:(Medium) rs1322693693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546973,Human_RBP_ID_774282,Human_RBP_ID_1584866,Human_RBP_ID_1913656,Human_RBP_ID_3620061,Human_RBP_ID_6900713,Human_RBP_ID_8515545,Human_RBP_ID_8846933,Human_RBP_ID_13820891,Human_RBP_ID_17275563,Human_RBP_ID_17390723,Human_RBP_ID_17506727,Human_RBP_ID_18193433,Human_RBP_ID_18443312,Human_RBP_ID_18757186,Human_RBP_ID_26819351,Human_RBP_ID_27009003,Human_RBP_ID_27288286,Human_RBP_ID_27478780 Human_miRNA_ID_2773543,Human_miRNA_ID_2948480 RMVar_hsa_circ_107101,RMVar_hsa_circ_208054 62403 RMVar_ID_62403 Human_SNP_ID_119258726 m1A Human chr2 + 241229393 241229393 241229393 CACGAATGCTCATGACCTTGGTTTAGTGTTAAACAGTGGAGCAGGTCCTGAGCGGGCACGGCCAG CACGAATGCTCATGACCTTGGTTTAGTGTTAAGCAGTGGAGCAGGTCCTGAGCGGGCACGGCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241229326..241229500 32194978 MeRIP-seq:(Medium) rs1381199050 Functional Loss SNV dbSNP153 33..33 33 - - - 62404 RMVar_ID_62404 Human_SNP_ID_119258732 m1A Human chr2 - 241229409 241229409 241229409 GGCCGCTCCTCCAGGCCTGGCCGTGCCCGCTCAGGACCTGCTCCACTGTTTAACACTAAACCAAG GGCCGCTCCTCCAGGCCTGGCCGTGCCCGCTCGGGACCTGCTCCACTGTTTAACACTAAACCAAG T C HDLBP Ensembl:ENSG00000115677 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:241229313..241229430 26863196 MeRIP-seq:(Medium) rs1441800469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242520,Human_RBP_ID_546973,Human_RBP_ID_1913659,Human_RBP_ID_8846935,Human_RBP_ID_17506727,Human_RBP_ID_18193434,Human_RBP_ID_27478782 RMVar_hsa_circ_107101,RMVar_hsa_circ_208054 62405 RMVar_ID_62405 Human_SNP_ID_119258980 m1A Human chr2 - 241229963 241229963 241229963 AGACTGACCCTGTCTTCCTGTCTTCTGCCTGCAGCTAGCTGACGTGGTGGACAGTGAGGCGCTGC AGACTGACCCTGTCTTCCTGTCTTCTGCCTGCCGCTAGCTGACGTGGTGGACAGTGAGGCGCTGC T G HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:241229831..241229965;chr2:241229826..241229975 26863196,32194978,32194978 MeRIP-seq:(Medium) rs941985041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57657,Human_RBP_ID_916935,Human_RBP_ID_5379003,Human_RBP_ID_22548002,Human_RBP_ID_22597446,Human_RBP_ID_22668271 RMVar_hsa_circ_208055,RMVar_hsa_circ_27144,RMVar_hsa_circ_107101,RMVar_hsa_circ_323740,RMVar_hsa_circ_361065,RMVar_hsa_circ_208054,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_54384,RMVar_hsa_circ_113256,RMVar_hsa_circ_35176,RMVar_hsa_circ_208057,RMVar_hsa_circ_208058,RMVar_hsa_circ_208056 62406 RMVar_ID_62406 Human_SNP_ID_119261140 m1A Human chr2 - 241236665 241236665 241236665 ACCCCGGCTCTCCAAGGAGGTGTGACATCATCATCATCTCTGGCCGGAAAGAAAAGTGTGAGGCT ACCCCGGCTCTCCAAGGAGGTGTGACATCATCTTCATCTCTGGCCGGAAAGAAAAGTGTGAGGCT T A HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241236572..241236719 26863196 MeRIP-seq:(Medium) rs746674954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57667,Human_RBP_ID_546992,Human_RBP_ID_1022571,Human_RBP_ID_1134691,Human_RBP_ID_1913679,Human_RBP_ID_3620073,Human_RBP_ID_3959978,Human_RBP_ID_4631430,Human_RBP_ID_8846972,Human_RBP_ID_9295699,Human_RBP_ID_9385843,Human_RBP_ID_17275575,Human_RBP_ID_17390730,Human_RBP_ID_17965805,Human_RBP_ID_18180370,Human_RBP_ID_18193438,Human_RBP_ID_18757203,Human_RBP_ID_22990915,Human_RBP_ID_26340513,Human_RBP_ID_27009048,Human_RBP_ID_27288303,Human_RBP_ID_27478801 Human_Splice_Rec_381297,Human_Splice_Rec_381351,Human_Splice_Rec_381405,Human_Splice_Rec_381459,Human_Splice_Rec_381491,Human_Splice_Rec_381529,Human_Splice_Rec_381553,Human_Splice_Rec_381569 Human_miRNA_ID_2064505,Human_miRNA_ID_2702380,Human_miRNA_ID_2933685 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_27144,RMVar_hsa_circ_107101,RMVar_hsa_circ_323740,RMVar_hsa_circ_208054,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_113256,RMVar_hsa_circ_35176,RMVar_hsa_circ_208057,RMVar_hsa_circ_208058,RMVar_hsa_circ_208056,RMVar_hsa_circ_208062,RMVar_hsa_circ_87225,RMVar_hsa_circ_114474,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_208061,RMVar_hsa_circ_89030,RMVar_hsa_circ_30135,RMVar_hsa_circ_336624,RMVar_hsa_circ_352648,RMVar_hsa_circ_79638,RMVar_hsa_circ_39483,RMVar_hsa_circ_60705,RMVar_hsa_circ_54737,RMVar_hsa_circ_113630,RMVar_hsa_circ_208067,RMVar_hsa_circ_208068,RMVar_hsa_circ_208066,RMVar_hsa_circ_114625,RMVar_hsa_circ_57770,RMVar_hsa_circ_78553,RMVar_hsa_circ_55360,RMVar_hsa_circ_92839,RMVar_hsa_circ_118015,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_208070,RMVar_hsa_circ_208075,RMVar_hsa_circ_82300,RMVar_hsa_circ_89716,RMVar_hsa_circ_208077,RMVar_hsa_circ_208078,RMVar_hsa_circ_208076,RMVar_hsa_circ_208074,RMVar_hsa_circ_63741,RMVar_hsa_circ_57322 62407 RMVar_ID_62407 Human_SNP_ID_119262254 m1A Human chr2 + 241240000 241240000 241240000 GTGATCAGGTCCTGGTCCTTGTCCTCAGCCGCAGGGAAGATGACACGTGCTCCAGTGCTGTCGCG GTGATCAGGTCCTGGTCCTTGTCCTCAGCCGCGGGGAAGATGACACGTGCTCCAGTGCTGTCGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241239951..241240021 26863196 MeRIP-seq:(Medium) rs764463016 Functional Loss SNV dbSNP153 33..33 33 - - - 62408 RMVar_ID_62408 Human_SNP_ID_119263055 m1A Human chr2 + 241242572 241242572 241242572 TTCCTGAACCTTCCACGGGAAAGTGAATGTGGACCCCGCCGCACTCCTCCATGATGGAGCGGATC TTCCTGAACCTTCCACGGGAAAGTGAATGTGGCCCCCGCCGCACTCCTCCATGATGGAGCGGATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr2:241242526..241242605;chr2:241242526..241242650 26863196,32194978 MeRIP-seq:(Medium) rs757259747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17953780 62409 RMVar_ID_62409 Human_SNP_ID_119266781 m1A Human chr2 - 241256277 241256277 241256277 CAGGAGACAGGCACGCGCATCAACATCCCCCCACCCAGCGTGAACCGGACAGAGATTGTCTTCAC CAGGAGACAGGCACGCGCATCAACATCCCCCCGCCCAGCGTGAACCGGACAGAGATTGTCTTCAC T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241256226..241256329 26863196 MeRIP-seq:(Medium) rs1369358723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_922589,Human_RBP_ID_5196345,Human_RBP_ID_8847024,Human_RBP_ID_9259973,Human_RBP_ID_17275601,Human_RBP_ID_17390744,Human_RBP_ID_18193441,Human_RBP_ID_26340536,Human_RBP_ID_27009102,Human_RBP_ID_27818154 Human_Splice_Rec_381269,Human_Splice_Rec_381323,Human_Splice_Rec_381379,Human_Splice_Rec_381431,Human_Splice_Rec_381503,Human_Splice_Rec_381631,Human_Splice_Rec_381645 Human_miRNA_ID_3002487 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_78553,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_63419,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_375899,RMVar_hsa_circ_279198,RMVar_hsa_circ_371246,RMVar_hsa_circ_208089,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_302446,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_208092,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_20829 62410 RMVar_ID_62410 Human_SNP_ID_119266790 m1A Human chr2 - 241256297 241256297 241256297 GACTGGTTGGCGAGATCATGCAGGAGACAGGCACGCGCATCAACATCCCCCCACCCAGCGTGAAC GACTGGTTGGCGAGATCATGCAGGAGACAGGCGCGCGCATCAACATCCCCCCACCCAGCGTGAAC T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241256176..241256345 26863196 MeRIP-seq:(Medium) rs1380894489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5196345,Human_RBP_ID_5589219,Human_RBP_ID_9259973,Human_RBP_ID_18193441,Human_RBP_ID_26340536 Human_miRNA_ID_2224906,Human_miRNA_ID_2652956,Human_miRNA_ID_2754152 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_78553,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_63419,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_375899,RMVar_hsa_circ_279198,RMVar_hsa_circ_371246,RMVar_hsa_circ_208089,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_302446,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_208092,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_20829 62411 RMVar_ID_62411 Human_SNP_ID_119269118 m1A Human chr2 + 241264428 241264426 241264429 ACATAGACATGTTACATGATAAAATTTTTAAAAGAAAGAATGGTGTTTCTACCTGAGTGATGACA ACATAGACATGTTACATGATAAAATTTTTAA___AAAGAATGGTGTTTCTACCTGAGTGATGACA AAAG A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241264426..241264500 32194978 MeRIP-seq:(Medium) rs1375661944 Functional Loss DEL dbSNP153 32..34 33 - - - 62412 RMVar_ID_62412 Human_SNP_ID_119269178 m1A Human chr2 + 241264604 241264604 241264604 GGGTCGCTCTCCTCTTCTGAATTTAGAGTGGCAACTGGACCAGCCAACACAGATTAAAAGGAAGC GGGTCGCTCTCCTCTTCTGAATTTAGAGTGGCCACTGGACCAGCCAACACAGATTAAAAGGAAGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241264576..241264625 32194978 MeRIP-seq:(Medium) rs1332259607 Functional Loss SNV dbSNP153 33..33 33 - - - 62413 RMVar_ID_62413 Human_SNP_ID_119271332 m1A Human chr2 + 241272530 241272527 241272530 TGTGCGCGCCCCTCCGCGCCACGGCCACGCGCAGAAGAGACTCGGAGCCGGCCCCAGGTCTGGCC TGTGCGCGCCCCTCCGCGCCACGGCCACGC___GAAGAGACTCGGAGCCGGCCCCAGGTCTGGCC CGCA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:241272518..241272850 26863196 MeRIP-seq:(Medium) rs1437013111 Functional Loss DEL dbSNP153 31..33 33 - - - 62414 RMVar_ID_62414 Human_SNP_ID_119271458 m1A Human chr2 - 241272716 241272703 241272716 CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGGACGGGGCGGGCGGGCTGCCGGGCGGGGGGGTGG CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGG_____________GCTGCCGGGCGGGGGGGTGG CCCGCCCGCCCCGT C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:241272702..241272825;chr2:241272707..241272850;chr2:241272705..241272850;chr2:241272705..241272825 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1200684284 Functional Loss DEL dbSNP153 33..45 33 - - - 62415 RMVar_ID_62415 Human_SNP_ID_119271467 m1A Human chr2 + 241272731 241272714 241272731 GCAGCCCGCCCGCCCCGTCCGCCCGCCCGCCCAGGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG GCAGCCCGCCCGCCCC_________________GGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG CGTCCGCCCGCCCGCCCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241272716..241272857 26863196 MeRIP-seq:(Medium) rs1226649138 Functional Loss DEL dbSNP153 17..33 33 - - - 62416 RMVar_ID_62416 Human_SNP_ID_119271470 m1A Human chr2 - 241272716 241272716 241272716 CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGGACGGGGCGGGCGGGCTGCCGGGCGGGGGGGTGG CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGGGCGGGGCGGGCGGGCTGCCGGGCGGGGGGGTGG T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:241272702..241272825;chr2:241272707..241272850;chr2:241272705..241272850;chr2:241272705..241272825 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1213169647 Functional Loss SNV dbSNP153 33..33 33 - - - 62417 RMVar_ID_62417 Human_SNP_ID_119271471 m1A Human chr2 - 241272716 241272716 241272716 CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGGACGGGGCGGGCGGGCTGCCGGGCGGGGGGGTGG CACGGGGCTGGGAGGCCTGGGCGGGCGGGCGGCCGGGGCGGGCGGGCTGCCGGGCGGGGGGGTGG T G HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:241272702..241272825;chr2:241272707..241272850;chr2:241272705..241272850;chr2:241272705..241272825 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1213169647 Functional Loss SNV dbSNP153 33..33 33 - - - 62418 RMVar_ID_62418 Human_SNP_ID_119271484 m1A Human chr2 + 241272731 241272731 241272731 GCAGCCCGCCCGCCCCGTCCGCCCGCCCGCCCAGGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG GCAGCCCGCCCGCCCCGTCCGCCCGCCCGCCCCGGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241272716..241272857 26863196 MeRIP-seq:(Medium) rs1195703099 Functional Loss SNV dbSNP153 33..33 33 - - - 62419 RMVar_ID_62419 Human_SNP_ID_119271485 m1A Human chr2 + 241272731 241272731 241272731 GCAGCCCGCCCGCCCCGTCCGCCCGCCCGCCCAGGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG GCAGCCCGCCCGCCCCGTCCGCCCGCCCGCCCGGGCCTCCCAGCCCCGTGTTGCGCGCTCACTCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241272716..241272857 26863196 MeRIP-seq:(Medium) rs1195703099 Functional Loss SNV dbSNP153 33..33 33 - - - 62420 RMVar_ID_62420 Human_SNP_ID_119281240 m1A Human chr2 + 241309899 241309899 241309899 AAGATATTTCTCTGGGGAATCTGAAGAAACCCAAAGAAGCTGACAAGGGTGCTGTAAGGAAATGG AAGATATTTCTCTGGGGAATCTGAAGAAACCCGAAGAAGCTGACAAGGGTGCTGTAAGGAAATGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241309895..241310000 32194978 MeRIP-seq:(Medium) rs1242675237 Functional Loss SNV dbSNP153 33..33 33 - - - 62421 RMVar_ID_62421 Human_SNP_ID_119282714 m1A Human chr2 - 241315153 241315152 241315153 TGCCCGGGCTGGGGCCCGCCGCCCCGCGGGGGAGGGCGGAGCTGGCGCGGCCCCTAGCTTTCTCC TGCCCGGGCTGGGGCCCGCCGCCCCGCGGGGG_GGGCGGAGCTGGCGCGGCCCCTAGCTTTCTCC CT C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241315101..241315200 26863196 MeRIP-seq:(Medium) rs1274672174 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_243500,Human_RBP_ID_4602466,Human_RBP_ID_5382419,Human_RBP_ID_8728799,Human_RBP_ID_18422061,Human_RBP_ID_18494682,Human_RBP_ID_26787557 Human_Splice_Rec_381419,Human_Splice_Rec_381711 62422 RMVar_ID_62422 Human_SNP_ID_119282867 m1A Human chr2 + 241315456 241315456 241315456 CCCCCTCCCCGTGATCGCTCCGCACTCCCGCCACCACCTGCCCTCCCGCGACCGCCTCTCTCCTC CCCCCTCCCCGTGATCGCTCCGCACTCCCGCCCCCACCTGCCCTCCCGCGACCGCCTCTCTCCTC A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:241315359..241315543 26863196 MeRIP-seq:(Medium) rs1207970364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5501939,Human_RBP_ID_9330877 RMVar_hsa_circ_93215,RMVar_hsa_circ_208100 62423 RMVar_ID_62423 Human_SNP_ID_119282921 m1A Human chr2 - 241315621 241315621 241315621 TTACCAAGATGGCGGCTTGTCCCTGTTTCGCCACAGTTCCTACCTTATGAGCTCGGTTTTCTTAT TTACCAAGATGGCGGCTTGTCCCTGTTTCGCCTCAGTTCCTACCTTATGAGCTCGGTTTTCTTAT T A HDLBP Ensembl:ENSG00000115677 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241315551..241315675 32194978 MeRIP-seq:(Medium) rs981826893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547050,Human_RBP_ID_4602488,Human_RBP_ID_5471509,Human_RBP_ID_8852230,Human_RBP_ID_9297003,Human_RBP_ID_9330878,Human_RBP_ID_18193584,Human_RBP_ID_18757291,Human_RBP_ID_26338904 Human_Splice_Rec_381311,Human_Splice_Rec_381657,Human_Splice_Rec_381731,Human_Splice_Rec_381741,Human_Splice_Rec_381767,Human_Splice_Rec_381805,Human_Splice_Rec_381813,Human_Splice_Rec_381823 62424 RMVar_ID_62424 Human_SNP_ID_119282922 m1A Human chr2 - 241315621 241315621 241315621 TTACCAAGATGGCGGCTTGTCCCTGTTTCGCCACAGTTCCTACCTTATGAGCTCGGTTTTCTTAT TTACCAAGATGGCGGCTTGTCCCTGTTTCGCCCCAGTTCCTACCTTATGAGCTCGGTTTTCTTAT T G HDLBP Ensembl:ENSG00000115677 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241315551..241315675 32194978 MeRIP-seq:(Medium) rs981826893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547050,Human_RBP_ID_4602488,Human_RBP_ID_5471509,Human_RBP_ID_8852230,Human_RBP_ID_9297003,Human_RBP_ID_9330878,Human_RBP_ID_18193584,Human_RBP_ID_18757291,Human_RBP_ID_26338904 Human_Splice_Rec_381311,Human_Splice_Rec_381657,Human_Splice_Rec_381731,Human_Splice_Rec_381741,Human_Splice_Rec_381767,Human_Splice_Rec_381805,Human_Splice_Rec_381813,Human_Splice_Rec_381823 62425 RMVar_ID_62425 Human_SNP_ID_119282929 m1A Human chr2 + 241315637 241315637 241315637 CATAAGGTAGGAACTGTGGCGAAACAGGGACAAGCCGCCATCTTGGTAAAGGAGAAGAGGCTACG CATAAGGTAGGAACTGTGGCGAAACAGGGACACGCCGCCATCTTGGTAAAGGAGAAGAGGCTACG A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241315323..241315675 26863196 MeRIP-seq:(Medium) rs879131414 Functional Loss SNV dbSNP153 33..33 33 - - - 62426 RMVar_ID_62426 Human_SNP_ID_119283141 m1A Human chr2 - 241315964 241315964 241315964 GGCGAGACACTCACCCGCCAAACAGCCCGAGAACAGGCGCCGACCGACCGCGCCGCGGACCCGCC GGCGAGACACTCACCCGCCAAACAGCCCGAGATCAGGCGCCGACCGACCGCGCCGCGGACCCGCC T A HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr2:241315936..241316086;chr2:241315901..241316167 26863196 MeRIP-seq:(Medium) rs914999836 Functional Loss SNV dbSNP153 33..33 33 - - - 62427 RMVar_ID_62427 Human_SNP_ID_119283147 m1A Human chr2 - 241315975 241315975 241315975 CGGGGTACACCGGCGAGACACTCACCCGCCAAACAGCCCGAGAACAGGCGCCGACCGACCGCGCC CGGGGTACACCGGCGAGACACTCACCCGCCAATCAGCCCGAGAACAGGCGCCGACCGACCGCGCC T A HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241315941..241316094 26863196 MeRIP-seq:(Medium) rs1191178882 Functional Loss SNV dbSNP153 33..33 33 - - - 62428 RMVar_ID_62428 Human_SNP_ID_119283154 m1A Human chr2 + 241315986 241315986 241315986 TCGGCGCCTGTTCTCGGGCTGTTTGGCGGGTGAGTGTCTCGCCGGTGTACCCCGCACAAGTTGTG TCGGCGCCTGTTCTCGGGCTGTTTGGCGGGTGTGTGTCTCGCCGGTGTACCCCGCACAAGTTGTG A T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:241315982..241316104 26863196 MeRIP-seq:(Medium) rs1160736992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264295,Human_RBP_ID_920033,Human_RBP_ID_8110063,Human_RBP_ID_8201144,Human_RBP_ID_8852231,Human_RBP_ID_9330879,Human_RBP_ID_9429481,Human_RBP_ID_17139473,Human_RBP_ID_18422063,Human_RBP_ID_18493957,Human_RBP_ID_19099078,Human_RBP_ID_22371321 RMVar_hsa_circ_117214,RMVar_hsa_circ_126739,RMVar_hsa_circ_208101,RMVar_hsa_circ_208102 62429 RMVar_ID_62429 Human_SNP_ID_119286267 m1A Human chr2 - 241325978 241325978 241325978 AAACTGAGTTGGCTGTTGCTAAATAAGATTAAAAAACAAACAAACTAATAAACACCTTAGTAGTT AAACTGAGTTGGCTGTTGCTAAATAAGATTAAGAAACAAACAAACTAATAAACACCTTAGTAGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr2:241325976..241326050 26863196,32194978 MeRIP-seq:(Medium) rs761097928 Functional Loss SNV dbSNP153 33..33 33 - - - 62430 RMVar_ID_62430 Human_SNP_ID_119286268 m1A Human chr2 - 241325978 241325978 241325978 AAACTGAGTTGGCTGTTGCTAAATAAGATTAAAAAACAAACAAACTAATAAACACCTTAGTAGTT AAACTGAGTTGGCTGTTGCTAAATAAGATTAACAAACAAACAAACTAATAAACACCTTAGTAGTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr2:241325976..241326050 26863196,32194978 MeRIP-seq:(Medium) rs761097928 Functional Loss SNV dbSNP153 33..33 33 - - - 62431 RMVar_ID_62431 Human_SNP_ID_119286290 m1A Human chr2 + 241326076 241326076 241326076 GCAAACCTCCCCAATCAAGTTCACCGAAAATCAGTGAAAAAAGGTTTTGAGTTCACACTGATGGT GCAAACCTCCCCAATCAAGTTCACCGAAAATCGGTGAAAAAAGGTTTTGAGTTCACACTGATGGT A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241326051..241326075 26863196 MeRIP-seq:(Medium) rs757016174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1913833,Human_RBP_ID_17278196,Human_RBP_ID_18757306,Human_RBP_ID_26664514 Human_Splice_Rec_381828,Human_Splice_Rec_381829,Human_Splice_Rec_381860,Human_Splice_Rec_381861,Human_Splice_Rec_381876,Human_Splice_Rec_381877,Human_Splice_Rec_381904,Human_Splice_Rec_381905,Human_Splice_Rec_381912,Human_Splice_Rec_381913,Human_Splice_Rec_381916,Human_Splice_Rec_381917,Human_Splice_Rec_381922,Human_Splice_Rec_381923,Human_Splice_Rec_381940,Human_Splice_Rec_381941,Human_Splice_Rec_381964,Human_Splice_Rec_381965,Human_Splice_Rec_381970,Human_Splice_Rec_381971,Human_Splice_Rec_381992,Human_Splice_Rec_381993,Human_Splice_Rec_382016,Human_Splice_Rec_382017,Human_Splice_Rec_382048,Human_Splice_Rec_382049,Human_Splice_Rec_382060,Human_Splice_Rec_382061,Human_Splice_Rec_382070,Human_Splice_Rec_382071,Human_Splice_Rec_382102,Human_Splice_Rec_382103,Human_Splice_Rec_382122,Human_Splice_Rec_382123,Human_Splice_Rec_382148,Human_Splice_Rec_382149,Human_Splice_Rec_382174,Human_Splice_Rec_382175,Human_Splice_Rec_382184,Human_Splice_Rec_382185,Human_Splice_Rec_382206,Human_Splice_Rec_382207,Human_Splice_Rec_382214,Human_Splice_Rec_382215,Human_Splice_Rec_382225,Human_Splice_Rec_382236,Human_Splice_Rec_382237,Human_Splice_Rec_382252,Human_Splice_Rec_382260,Human_Splice_Rec_382261,Human_Splice_Rec_382270,Human_Splice_Rec_382271,Human_Splice_Rec_382280,Human_Splice_Rec_382281 Human_miRNA_ID_241282,Human_miRNA_ID_3097055,Human_miRNA_ID_3097056 RMVar_hsa_circ_208107,RMVar_hsa_circ_55220,RMVar_hsa_circ_117214,RMVar_hsa_circ_126739,RMVar_hsa_circ_124486,RMVar_hsa_circ_208101,RMVar_hsa_circ_208102,RMVar_hsa_circ_208103,RMVar_hsa_circ_81533,RMVar_hsa_circ_208106,RMVar_hsa_circ_62796,RMVar_hsa_circ_349631,RMVar_hsa_circ_29898,RMVar_hsa_circ_329789,RMVar_hsa_circ_318368,RMVar_hsa_circ_208104,RMVar_hsa_circ_348204,RMVar_hsa_circ_310151,RMVar_hsa_circ_283685,RMVar_hsa_circ_326498,RMVar_hsa_circ_208105,RMVar_hsa_circ_363951,RMVar_hsa_circ_294519,RMVar_hsa_circ_276747,RMVar_hsa_circ_278694,RMVar_hsa_circ_275956,RMVar_hsa_circ_208109,RMVar_hsa_circ_208111,RMVar_hsa_circ_208113,RMVar_hsa_circ_208114,RMVar_hsa_circ_208112,RMVar_hsa_circ_208110,RMVar_hsa_circ_208108 62432 RMVar_ID_62432 Human_SNP_ID_119289100 m1A Human chr2 - 241335146 241335146 241335146 ATCAGTTAGGAATAGGCTGTTTATGAGAGTCGATTTTCCTAGACCTGATTCACCTTTAAATAAAA ATCAGTTAGGAATAGGCTGTTTATGAGAGTCGCTTTTCCTAGACCTGATTCACCTTTAAATAAAA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241326084..241335247 32194978 MeRIP-seq:(Medium) rs762942157 Functional Loss SNV dbSNP153 33..33 33 - - - 62433 RMVar_ID_62433 Human_SNP_ID_119289410 m1A Human chr2 - 241336047 241336047 241336047 CGTCACCATAGCCAGGGGTATCTACCACTGTCAGGCGTAGCTTGACCCCTCGCTCTTCAATTTCA CGTCACCATAGCCAGGGGTATCTACCACTGTCGGGCGTAGCTTGACCCCTCGCTCTTCAATTTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241335996..241336146 32194978 MeRIP-seq:(Medium) rs1418689196 Functional Loss SNV dbSNP153 33..33 33 - - - 62434 RMVar_ID_62434 Human_SNP_ID_119292141 m1A Human chr2 - 241343841 241343841 241343841 AAGTCATTGTGCTCTGGGTTCTCCACTTCCACAACACCCCAGGGGTAGAGGCGGCCTCTGACCTT AAGTCATTGTGCTCTGGGTTCTCCACTTCCACCACACCCCAGGGGTAGAGGCGGCCTCTGACCTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241337658..241346284 32194978 MeRIP-seq:(Medium) rs1478397519 Functional Loss SNV dbSNP153 33..33 33 - - - 62435 RMVar_ID_62435 Human_SNP_ID_119293948 m1A Human chr2 - 241350116 241350110 241350116 CATCGCCATCCCCGCCCTGCATCTGCATCTGCATCTGCGCCTGCATCCTTGCAATCATCTCTTGC CATCGCCATCCCCGCCCTGCATCTGCATCTGC______GCCTGCATCCTTGCAATCATCTCTTGC CGCAGAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241350083..241350155 26863196 MeRIP-seq:(Medium) rs772812693 Functional Loss DEL dbSNP153 33..38 33 - - - 62436 RMVar_ID_62436 Human_SNP_ID_119293953 m1A Human chr2 - 241350116 241350116 241350116 CATCGCCATCCCCGCCCTGCATCTGCATCTGCATCTGCGCCTGCATCCTTGCAATCATCTCTTGC CATCGCCATCCCCGCCCTGCATCTGCATCTGCGTCTGCGCCTGCATCCTTGCAATCATCTCTTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241350083..241350155 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 62437 RMVar_ID_62437 Human_SNP_ID_119293984 m1A Human chr2 + 241350185 241350185 241350185 GGCTCTCGGGCACCACGTGTAAGGTGATGTGCACATATCAAGAAGTCAGAGGTAGGCCCTGTTGT GGCTCTCGGGCACCACGTGTAAGGTGATGTGCGCATATCAAGAAGTCAGAGGTAGGCCCTGTTGT A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241350051..241350225 32194978 MeRIP-seq:(Medium) rs201771016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547102,Human_RBP_ID_920397,Human_RBP_ID_1022601,Human_RBP_ID_1585022,Human_RBP_ID_1913920,Human_RBP_ID_3958600,Human_RBP_ID_9104718,Human_RBP_ID_13824134,Human_RBP_ID_17965086,Human_RBP_ID_23862285,Human_RBP_ID_26340543,Human_RBP_ID_27694250 Human_Splice_Rec_381847,Human_Splice_Rec_381895,Human_Splice_Rec_381959,Human_Splice_Rec_382013,Human_Splice_Rec_382035,Human_Splice_Rec_382141,Human_Splice_Rec_382167,Human_Splice_Rec_382307,Human_Splice_Rec_382315 Human_miRNA_ID_456126,Human_miRNA_ID_458086,Human_miRNA_ID_2147846,Human_miRNA_ID_2148646 RMVar_hsa_circ_33028,RMVar_hsa_circ_109430,RMVar_hsa_circ_208121,RMVar_hsa_circ_55957,RMVar_hsa_circ_103836,RMVar_hsa_circ_208126,RMVar_hsa_circ_75722,RMVar_hsa_circ_208128,RMVar_hsa_circ_124715,RMVar_hsa_circ_378827,RMVar_hsa_circ_208129 62438 RMVar_ID_62438 Human_SNP_ID_119299775 m1A Human chr2 - 241373060 241373060 241373060 AAGAAAACACTAAAATGAAAAAAAAAAAAACCACATGAAGGAATTATCACATTATTTAGGTACTA AAGAAAACACTAAAATGAAAAAAAAAAAAACCTCATGAAGGAATTATCACATTATTTAGGTACTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241373058..241373123 26863196 MeRIP-seq:(Medium) rs775418921 Functional Loss SNV dbSNP153 33..33 33 - - - 62439 RMVar_ID_62439 Human_SNP_ID_119299813 m1A Human chr2 + 241373128 241373128 241373128 TCATGGTGAAGAATGGGGGAGATAGAAGGAACATACAGAGTCCTGCAGACTGCAGGGATGCGCTT TCATGGTGAAGAATGGGGGAGATAGAAGGAACCTACAGAGTCCTGCAGACTGCAGGGATGCGCTT A C FARP2 Ensembl:ENSG00000006607 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241373039..241373132 26863196 MeRIP-seq:(Medium) rs139981990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4602676,Human_RBP_ID_19001032,Human_RBP_ID_26340544,Human_RBP_ID_27009234 Human_Splice_Rec_382322,Human_Splice_Rec_382374,Human_Splice_Rec_382408,Human_Splice_Rec_382418,Human_Splice_Rec_382452,Human_Splice_Rec_382456,Human_Splice_Rec_382460 RMVar_hsa_circ_40736,RMVar_hsa_circ_298757,RMVar_hsa_circ_109114,RMVar_hsa_circ_208130,RMVar_hsa_circ_208131 62440 RMVar_ID_62440 Human_SNP_ID_119303030 m1A Human chr2 + 241386563 241386562 241386564 TTTAAAGATTGGTTAGCGATTGTCAAAGGGAAAGGGGAGGTTTGGAAAGCCCCCTGGGCATGTGC TTTAAAGATTGGTTAGCGATTGTCAAAGGGAA__GGGAGGTTTGGAAAGCCCCCTGGGCATGTGC AAG A FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241386557..241386658 26863196 MeRIP-seq:(Medium) rs1179191368 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_40736,RMVar_hsa_circ_109114,RMVar_hsa_circ_208131 62441 RMVar_ID_62441 Human_SNP_ID_119303031 m1A Human chr2 + 241386563 241386563 241386563 TTTAAAGATTGGTTAGCGATTGTCAAAGGGAAAGGGGAGGTTTGGAAAGCCCCCTGGGCATGTGC TTTAAAGATTGGTTAGCGATTGTCAAAGGGAACGGGGAGGTTTGGAAAGCCCCCTGGGCATGTGC A C FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241386557..241386658 26863196 MeRIP-seq:(Medium) rs939168031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40736,RMVar_hsa_circ_109114,RMVar_hsa_circ_208131 62442 RMVar_ID_62442 Human_SNP_ID_119307259 m1A Human chr2 + 241403916 241403915 241403917 AGAATGTGACTACTTCGGGATGGAGTTTCAAAATACTCAGTCCTACTGGGTAAGTGCTTATGACG AGAATGTGACTACTTCGGGATGGAGTTTCAAA__ACTCAGTCCTACTGGGTAAGTGCTTATGACG AAT A FARP2 Ensembl:ENSG00000006607 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241403878..241405255 32194978 MeRIP-seq:(Medium) rs1363821342 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_916939,Human_RBP_ID_1585052,Human_RBP_ID_5380418,Human_RBP_ID_9385927 Human_Splice_Rec_382324,Human_Splice_Rec_382325,Human_Splice_Rec_382376,Human_Splice_Rec_382377,Human_Splice_Rec_382412,Human_Splice_Rec_382413,Human_Splice_Rec_382420,Human_Splice_Rec_382421,Human_Splice_Rec_382462,Human_Splice_Rec_382463,Human_Splice_Rec_382468,Human_Splice_Rec_382472,Human_Splice_Rec_382474,Human_Splice_Rec_382475,Human_Splice_Rec_382482,Human_Splice_Rec_382483 RMVar_hsa_circ_40736,RMVar_hsa_circ_109114,RMVar_hsa_circ_208137,RMVar_hsa_circ_270405,RMVar_hsa_circ_306744,RMVar_hsa_circ_208131,RMVar_hsa_circ_315261,RMVar_hsa_circ_337148,RMVar_hsa_circ_358423,RMVar_hsa_circ_310879,RMVar_hsa_circ_278744,RMVar_hsa_circ_289644,RMVar_hsa_circ_272371,RMVar_hsa_circ_208141,RMVar_hsa_circ_75502,RMVar_hsa_circ_77783,RMVar_hsa_circ_37702,RMVar_hsa_circ_208142,RMVar_hsa_circ_208139,RMVar_hsa_circ_208140,RMVar_hsa_circ_208138,RMVar_hsa_circ_208133,RMVar_hsa_circ_208135,RMVar_hsa_circ_208136,RMVar_hsa_circ_208134,RMVar_hsa_circ_208132 62443 RMVar_ID_62443 Human_SNP_ID_119313213 m1A Human chr2 - 241426543 241426542 241426544 TCCATTCATTCACCCGTATTTCTGAAAAGCACATTTATGACAGCTAGCACATTCTCCACTTTGAA TCCATTCATTCACCCGTATTTCTGAAAAGCA__TTTATGACAGCTAGCACATTCTCCACTTTGAA ATG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241426530..241426618 26863196 MeRIP-seq:(Medium) rs1480291953 Functional Loss DEL dbSNP153 32..33 33 - - - 62444 RMVar_ID_62444 Human_SNP_ID_119317317 m1A Human chr2 - 241441379 241441379 241441379 AAACTCTGGCAGGCCAGAGGGGACCAGAGTGGAGGGAGAGAGCGAGTAAAAGGCATTCGCTGAAG AAACTCTGGCAGGCCAGAGGGGACCAGAGTGGCGGGAGAGAGCGAGTAAAAGGCATTCGCTGAAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241436536..241441451 32194978 MeRIP-seq:(Medium) rs971097956 Functional Loss SNV dbSNP153 33..33 33 - - - 62445 RMVar_ID_62445 Human_SNP_ID_119317625 m1A Human chr2 + 241442246 241442246 241442246 GCAGCTCAGCCAGTCAATCTGAGGCCAGCTCCATGGTCAACTTCCCAGCCTACTCAGTCCGCTCT GCAGCTCAGCCAGTCAATCTGAGGCCAGCTCCCTGGTCAACTTCCCAGCCTACTCAGTCCGCTCT A C FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241442198..241442349 32194978 MeRIP-seq:(Medium) rs1213538702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1022620,Human_RBP_ID_18757385 RMVar_hsa_circ_13459,RMVar_hsa_circ_358423,RMVar_hsa_circ_77783,RMVar_hsa_circ_208133,RMVar_hsa_circ_208132,RMVar_hsa_circ_99116,RMVar_hsa_circ_80775,RMVar_hsa_circ_208144,RMVar_hsa_circ_127707,RMVar_hsa_circ_208143,RMVar_hsa_circ_208153,RMVar_hsa_circ_100772,RMVar_hsa_circ_208157,RMVar_hsa_circ_110193,RMVar_hsa_circ_338599,RMVar_hsa_circ_208162 62446 RMVar_ID_62446 Human_SNP_ID_119329113 m1A Human chr2 + 241485285 241485238 241485286 GGGATCCTCCTTTCCTAGGATCTTCCCTCCCTAGAGTCCTCCCTCCCTCCCTGGGATCTTCCCTT __________________________________AGTCCTCCCTCCCTCCCTGGGATCTTCCCTT TAGTCCTCCCTCCCTGGGATCCTCCTTTCCTAGGATCTTCCCTCCCTAG T FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241485265..241485468 26863196 MeRIP-seq:(Medium) rs1365931881 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5131748,Human_RBP_ID_17084795,Human_RBP_ID_18950007 RMVar_hsa_circ_6096,RMVar_hsa_circ_80775,RMVar_hsa_circ_208143,RMVar_hsa_circ_110193,RMVar_hsa_circ_99108,RMVar_hsa_circ_208162,RMVar_hsa_circ_76198,RMVar_hsa_circ_208164,RMVar_hsa_circ_126541,RMVar_hsa_circ_208165,RMVar_hsa_circ_64177,RMVar_hsa_circ_24686,RMVar_hsa_circ_208171,RMVar_hsa_circ_208172,RMVar_hsa_circ_122018 62447 RMVar_ID_62447 Human_SNP_ID_119332248 m1A Human chr2 - 241495069 241495069 241495069 TGAAATATTCTGAGGTTAATATGTTAGTTTTCATAGAACATTGAGAGGCCCCTGCCACTTTCAAT TGAAATATTCTGAGGTTAATATGTTAGTTTTCGTAGAACATTGAGAGGCCCCTGCCACTTTCAAT T C STK25 Ensembl:ENSG00000115694 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241494918..241495069 32194978 MeRIP-seq:(Medium) rs567240244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547243,Human_RBP_ID_1913993,Human_RBP_ID_3620442,Human_RBP_ID_4602766,Human_RBP_ID_5118218,Human_RBP_ID_13825406,Human_RBP_ID_23211858,Human_RBP_ID_23862452,Human_RBP_ID_24421435,Human_RBP_ID_24488715,Human_RBP_ID_26487734 RMVar_hsa_circ_208173,RMVar_hsa_circ_92368 62448 RMVar_ID_62448 Human_SNP_ID_119332306 m1A Human chr2 - 241495267 241495267 241495267 AGCTCTGCCTCCTCCTCCCATGAGGTGGGGAGAGGCAACAGGGCAGCCCCCAGAGGAGTGTCCTG AGCTCTGCCTCCTCCTCCCATGAGGTGGGGAGCGGCAACAGGGCAGCCCCCAGAGGAGTGTCCTG T G STK25 Ensembl:ENSG00000115694 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241495217..241497254 32194978 MeRIP-seq:(Medium) rs769530113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623052,Human_RBP_ID_18193446,Human_RBP_ID_23862458,Human_RBP_ID_27009288,Human_RBP_ID_27288428 Human_miRNA_ID_3089872 RMVar_hsa_circ_208173,RMVar_hsa_circ_92368 62449 RMVar_ID_62449 Human_SNP_ID_119332724 m1A Human chr2 + 241496491 241496491 241496491 CGGCCAGGCTGAAGGCGTTCTCCAGCTCCTCCAGCGCACCCACGCTCCCGCCGCTCTGCTTGTGC CGGCCAGGCTGAAGGCGTTCTCCAGCTCCTCCCGCGCACCCACGCTCCCGCCGCTCTGCTTGTGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241496443..241496578 26863196 MeRIP-seq:(Medium) rs1179240161 Functional Loss SNV dbSNP153 33..33 33 - - - 62450 RMVar_ID_62450 Human_SNP_ID_119334188 m1A Human chr2 + 241500877 241500877 241500877 ATGCTCCAGGGTGGGAGTCACAGGCCGGAGTCAGCCAGGGCCCAGGCCCCACCGGTCCCATCCCT ATGCTCCAGGGTGGGAGTCACAGGCCGGAGTCCGCCAGGGCCCAGGCCCCACCGGTCCCATCCCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241500872..241501073 32194978 MeRIP-seq:(Medium) rs1004342158 Functional Loss SNV dbSNP153 33..33 33 - - - 62451 RMVar_ID_62451 Human_SNP_ID_119334189 m1A Human chr2 + 241500877 241500877 241500877 ATGCTCCAGGGTGGGAGTCACAGGCCGGAGTCAGCCAGGGCCCAGGCCCCACCGGTCCCATCCCT ATGCTCCAGGGTGGGAGTCACAGGCCGGAGTCGGCCAGGGCCCAGGCCCCACCGGTCCCATCCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241500872..241501073 32194978 MeRIP-seq:(Medium) rs1004342158 Functional Loss SNV dbSNP153 33..33 33 - - - 62452 RMVar_ID_62452 Human_SNP_ID_119336509 m1A Human chr2 + 241508367 241508367 241508367 CCTCCCGGTGCCCCCGCCCCGGTGTCCCCGCCACCGAGCCCCGCCCCGGGCCCCTCCCTCTGCCC CCTCCCGGTGCCCCCGCCCCGGTGTCCCCGCCCCCGAGCCCCGCCCCGGGCCCCTCCCTCTGCCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:241508364..241508575 26863196 MeRIP-seq:(Medium) rs564119331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208180 62453 RMVar_ID_62453 Human_SNP_ID_119336510 m1A Human chr2 + 241508367 241508367 241508367 CCTCCCGGTGCCCCCGCCCCGGTGTCCCCGCCACCGAGCCCCGCCCCGGGCCCCTCCCTCTGCCC CCTCCCGGTGCCCCCGCCCCGGTGTCCCCGCCGCCGAGCCCCGCCCCGGGCCCCTCCCTCTGCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:241508364..241508575 26863196 MeRIP-seq:(Medium) rs564119331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208180 62454 RMVar_ID_62454 Human_SNP_ID_119339249 m1A Human chr2 + 241516966 241516966 241516966 CCAACACACACACAAACACACCCAACACACACACACCCAACACACACCCCCAACACACACACCCC CCAACACACACACAAACACACCCAACACACACCCACCCAACACACACCCCCAACACACACACCCC A C HSALNG0023694 RNACentral:URS0000E94C62 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241516889..241517109 26863196 MeRIP-seq:(Medium) rs1459191633 Functional Loss SNV dbSNP153 33..33 33 - - - 62455 RMVar_ID_62455 Human_SNP_ID_119350528 m1A Human chr2 + 241558818 241558818 241558818 CAGGCCCCCGACGCCGCGGCAGGAGCCCCCCAAGAGCGCGGGAAGCCCCGTGGACCTGGCGCTCC CAGGCCCCCGACGCCGCGGCAGGAGCCCCCCATGAGCGCGGGAAGCCCCGTGGACCTGGCGCTCC A T BOK Ensembl:ENSG00000176720 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241558776..241558895 26863196 MeRIP-seq:(Medium) rs971929748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127107,RMVar_hsa_circ_208181 62456 RMVar_ID_62456 Human_SNP_ID_119350765 m1A Human chr2 - 241559422 241559422 241559422 CTGCGGGCACAAGCGCTCAGCCGGGTGGAGGGAGGCGGCGCGGGGAACGGGGCGCGCGGGGCGCC CTGCGGGCACAAGCGCTCAGCCGGGTGGAGGGGGGCGGCGCGGGGAACGGGGCGCGCGGGGCGCC T C BOK-AS1 RNACentral:URS00008B9745 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241559417..241559501 26863196 MeRIP-seq:(Medium) rs1295612272 Functional Loss SNV dbSNP153 33..33 33 - - - 62457 RMVar_ID_62457 Human_SNP_ID_119351648 m1A Human chr2 - 241562166 241562166 241562166 ACCCCATCTGACCTCCCTTGGGCCATCCCCCAACCTTGGCCCCTAGGGACCAGAAGACCAAGGAA ACCCCATCTGACCTCCCTTGGGCCATCCCCCAGCCTTGGCCCCTAGGGACCAGAAGACCAAGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241562158..241562328 26863196 MeRIP-seq:(Medium) rs1342773958 Functional Loss SNV dbSNP153 33..33 33 - - - 62458 RMVar_ID_62458 Human_SNP_ID_119352382 m1A Human chr2 - 241564574 241564574 241564574 GCCCACTGTGCCGTGAACCCTGCCCCCTGCCCACCCGGCCCCTGAGCCACACCACCTGCCCACTC GCCCACTGTGCCGTGAACCCTGCCCCCTGCCCCCCCGGCCCCTGAGCCACACCACCTGCCCACTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241564558..241564827 26863196 MeRIP-seq:(Medium) rs1210739230 Functional Loss SNV dbSNP153 33..33 33 - - - 62459 RMVar_ID_62459 Human_SNP_ID_119354162 m1A Human chr2 + 241570438 241570438 241570438 CGAGGGTACAGACGTACGGGAGGGAGTGGCGGATGGGTGAGTGTCTGAGCGCCTGGGGGGTGGGA CGAGGGTACAGACGTACGGGAGGGAGTGGCGGGTGGGTGAGTGTCTGAGCGCCTGGGGGGTGGGA A G BOK Ensembl:ENSG00000176720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241570422..241570538 26863196 MeRIP-seq:(Medium) rs113164348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8201179 RMVar_hsa_circ_84439,RMVar_hsa_circ_127107,RMVar_hsa_circ_208181,RMVar_hsa_circ_208182 62460 RMVar_ID_62460 Human_SNP_ID_119354173 m1A Human chr2 - 241570459 241570459 241570459 TGCACCCTCGCACCCCAGCTCTCCCACCCCCCAGGCGCTCAGACACTCACCCATCCGCCACTCCC TGCACCCTCGCACCCCAGCTCTCCCACCCCCCCGGCGCTCAGACACTCACCCATCCGCCACTCCC T G HSALNG0023700 RNACentral:URS0000EB388D lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241570282..241570557 26863196 MeRIP-seq:(Medium) rs966992799 Functional Loss SNV dbSNP153 33..33 33 - - - 62461 RMVar_ID_62461 Human_SNP_ID_119354301 m1A Human chr2 + 241570973 241570973 241570973 CGAGGGTGCAGAGGTACAGGAGGGAGTGGCGGATGGGTGAGTGTCTGAGCGCCTGTGGGGGTGGG CGAGGGTGCAGAGGTACAGGAGGGAGTGGCGGGTGGGTGAGTGTCTGAGCGCCTGTGGGGGTGGG A G BOK Ensembl:ENSG00000176720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241570972..241571159 26863196 MeRIP-seq:(Medium) rs1370213564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84439,RMVar_hsa_circ_127107,RMVar_hsa_circ_208181,RMVar_hsa_circ_208182 62462 RMVar_ID_62462 Human_SNP_ID_119355167 m1A Human chr2 + 241573483 241573476 241573484 CTGGCCTGGCTGAAGCTGGAAGAGCTGTGGGGACTCAGCCTGTAAACAGAGCGTAAGGTTCACAT CTGGCCTGGCTGAAGCTGGAAGAGCT________TCAGCCTGTAAACAGAGCGTAAGGTTCACAT TGTGGGGAC T BOK Ensembl:ENSG00000176720 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:241572976..241573497 32194978 MeRIP-seq:(Medium) rs1237304209 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_8202621 RMVar_hsa_circ_84439,RMVar_hsa_circ_127107,RMVar_hsa_circ_208181,RMVar_hsa_circ_208182 62463 RMVar_ID_62463 Human_SNP_ID_119365640 m1A Human chr2 + 241610215 241610215 241610215 CCCACGAGGCAGGACAGCCCCGGGCTAGGGTGAGGGGCACGCGCCGCAAGTCCTGCCTCTGCTCC CCCACGAGGCAGGACAGCCCCGGGCTAGGGTGTGGGGCACGCGCCGCAAGTCCTGCCTCTGCTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241610213..241610702 26863196 MeRIP-seq:(Medium) rs981909157 Functional Loss SNV dbSNP153 33..33 33 - - - 62464 RMVar_ID_62464 Human_SNP_ID_119365665 m1A Human chr2 - 241610260 241610260 241610260 TGCGCTTCCGGGGCGGGGCCGGCGGAGGCTGGAGGGGGCCGCCCGGGAGCAGAGGCAGGACTTGC TGCGCTTCCGGGGCGGGGCCGGCGGAGGCTGGGGGGGGCCGCCCGGGAGCAGAGGCAGGACTTGC T C THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241610255..241610379 26863196 MeRIP-seq:(Medium) rs995776462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_84329,RMVar_hsa_circ_338904,RMVar_hsa_circ_208190,RMVar_hsa_circ_342575 62465 RMVar_ID_62465 Human_SNP_ID_119368684 m1A Human chr2 - 241620381 241620381 241620381 GACTCACTCTCCCCTCACTCACTGACTCACTCACCCCTCACCCCTCACTCACCGACTCACTCACC GACTCACTCTCCCCTCACTCACTGACTCACTCCCCCCTCACCCCTCACTCACCGACTCACTCACC T G THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241620377..241620654 26863196 MeRIP-seq:(Medium) rs1368255956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2632770 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_342575 62466 RMVar_ID_62466 Human_SNP_ID_119368738 m1A Human chr2 - 241620524 241620524 241620524 GACTCACTCACCCCTCAGTCACCGACTCACTCACCCCTCACTCACTCCTCACTCACCCCTCACTC GACTCACTCACCCCTCAGTCACCGACTCACTCCCCCCTCACTCACTCCTCACTCACCCCTCACTC T G THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241620522..241620606 26863196 MeRIP-seq:(Medium) rs1313062816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205065,Human_RBP_ID_1068091,Human_RBP_ID_26760723 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_342575 62467 RMVar_ID_62467 Human_SNP_ID_119368740 m1A Human chr2 - 241620536 241620533 241620536 TCACTCACTCCTGACTCACTCACCCCTCAGTCACCGACTCACTCACCCCTCACTCACTCCTCACT TCACTCACTCCTGACTCACTCACCCCTCAGTC___GACTCACTCACCCCTCACTCACTCCTCACT CGGT C THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241620532..241620639 26863196 MeRIP-seq:(Medium) rs1280169706 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_205065,Human_RBP_ID_1068091,Human_RBP_ID_9429116,Human_RBP_ID_26761238 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_342575 62468 RMVar_ID_62468 Human_SNP_ID_119370827 m1A Human chr2 - 241627955 241627955 241627955 TGGAGTGAGGCAAGTAGACAGGAGCCAGAGGGAGTGTGGCTCCAAAGAGAGTGTGTCAGTGGGGA TGGAGTGAGGCAAGTAGACAGGAGCCAGAGGGGGTGTGGCTCCAAAGAGAGTGTGTCAGTGGGGA T C THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241627953..241628540 26863196 MeRIP-seq:(Medium) rs150034230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_342575 62469 RMVar_ID_62469 Human_SNP_ID_119372299 m1A Human chr2 + 241633039 241633039 241633039 CGGAGCGGCTGACCCTCTGCCGCAGGCTCTTCAGCTCGCCGTTCTTCTTCTCCACCTGCTCCCGC CGGAGCGGCTGACCCTCTGCCGCAGGCTCTTCGGCTCGCCGTTCTTCTTCTCCACCTGCTCCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr2:241632901..241633100;chr2:241632989..241633340 26863196,32194978 MeRIP-seq:(Medium) rs963145223 Functional Loss SNV dbSNP153 33..33 33 - - - 62470 RMVar_ID_62470 Human_SNP_ID_119372362 m1A Human chr2 - 241633187 241633187 241633187 CGGAAGCCGTGCAGAGCGAGCACAGCGACGCCAGCCCCATGTCCATCAACGAGGTCATCCTGTCG CGGAAGCCGTGCAGAGCGAGCACAGCGACGCCCGCCCCATGTCCATCAACGAGGTCATCCTGTCG T G THAP4 Ensembl:ENSG00000176946 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241633136..241633400 26863196 MeRIP-seq:(Medium) rs755784876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_144691,Human_RBP_ID_1195460,Human_RBP_ID_4602922 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_273583,RMVar_hsa_circ_342575,RMVar_hsa_circ_208191 62471 RMVar_ID_62471 Human_SNP_ID_119372584 m1A Human chr2 - 241633745 241633745 241633745 GGTCACCGTCCTCGAGTGGAAACCCGATGGCCAAGCCAGAGTCCCGCAGGTTGAAGCAAGCTGCT GGTCACCGTCCTCGAGTGGAAACCCGATGGCCGAGCCAGAGTCCCGCAGGTTGAAGCAAGCTGCT T C THAP4 Ensembl:ENSG00000176946 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241633695..241633850 26863196 MeRIP-seq:(Medium) rs763395081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17954040,Human_RBP_ID_23862526 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_273583,RMVar_hsa_circ_342575,RMVar_hsa_circ_208191 62472 RMVar_ID_62472 Human_SNP_ID_119372606 m1A Human chr2 - 241633796 241633796 241633796 GGGGTGTGAGGGGACACTCGAGTGCCGCCACCAGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG GGGGTGTGAGGGGACACTCGAGTGCCGCCACCGGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG T C THAP4 Ensembl:ENSG00000176946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241633746..241634100 26863196 MeRIP-seq:(Medium) rs7424328 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4625286,Human_RBP_ID_17965088,Human_RBP_ID_19001057 Human_miRNA_ID_2050651 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_273583,RMVar_hsa_circ_342575,RMVar_hsa_circ_208191 62473 RMVar_ID_62473 Human_SNP_ID_119372607 m1A Human chr2 - 241633796 241633796 241633796 GGGGTGTGAGGGGACACTCGAGTGCCGCCACCAGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG GGGGTGTGAGGGGACACTCGAGTGCCGCCACCCGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG T G THAP4 Ensembl:ENSG00000176946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241633746..241634100 26863196 MeRIP-seq:(Medium) rs7424328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625286,Human_RBP_ID_17965088,Human_RBP_ID_19001057 Human_miRNA_ID_2050651 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_273583,RMVar_hsa_circ_342575,RMVar_hsa_circ_208191 62474 RMVar_ID_62474 Human_SNP_ID_119373651 m1A Human chr2 - 241636905 241636905 241636905 CGCGGGCCCCGGGCCGCCACGCCCCCGCCCCGACCCGGCCCTGCGGGGAAACTGAGGCCCCGCGG CGCGGGCCCCGGGCCGCCACGCCCCCGCCCCGCCCCGGCCCTGCGGGGAAACTGAGGCCCCGCGG T G THAP4 Ensembl:ENSG00000176946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241636903..241637055 26863196 MeRIP-seq:(Medium) rs577654899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19103388,Human_RBP_ID_26787586 62475 RMVar_ID_62475 Human_SNP_ID_119383502 m1A Human chr2 - 241667285 241667285 241667285 TGCTTTCATGACATGGGGGAGCCTGTGGCTGGAGCTCCTCACACAGCCCTGCCCATCCCCAGGCC TGCTTTCATGACATGGGGGAGCCTGTGGCTGGCGCTCCTCACACAGCCCTGCCCATCCCCAGGCC T G lnc-DTYMK-2 RNACentral:URS0000D6D650 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241667235..241667323 26863196 MeRIP-seq:(Medium) rs981617287 Functional Loss SNV dbSNP153 33..33 33 - - - 62476 RMVar_ID_62476 Human_SNP_ID_119385086 m1A Human chr2 - 241671759 241671759 241671759 GCTGGCCATGGTCCGAGGGGTCTACGCCACCCATGGCCAGTGGTGCCCAAGTGAACCAGTCCCCC GCTGGCCATGGTCCGAGGGGTCTACGCCACCCGTGGCCAGTGGTGCCCAAGTGAACCAGTCCCCC T C lnc-DTYMK-2 RNACentral:URS0000D6D650 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241671709..241671824 26863196 MeRIP-seq:(Medium) rs1323219994 Functional Loss SNV dbSNP153 33..33 33 - - - 62477 RMVar_ID_62477 Human_SNP_ID_119386571 m1A Human chr2 + 241675938 241675938 241675938 GCTCCATCGCTCTGCTCATGTCCACACTGCCAAGGTCCCCACCACGGGGGTCCCCAGTGCACCCC GCTCCATCGCTCTGCTCATGTCCACACTGCCAGGGTCCCCACCACGGGGGTCCCCAGTGCACCCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:241675801..241676025 32194978 MeRIP-seq:(Medium) rs1270264884 Functional Loss SNV dbSNP153 33..33 33 - - - 62478 RMVar_ID_62478 Human_SNP_ID_119388704 m1A Human chr2 - 241682911 241682911 241682911 TATTTCTTTTTTGTTTTCCTCGAGACAGTTTCATTCTTGTCGCCCAGACTGGAGTGCAATGGGGC TATTTCTTTTTTGTTTTCCTCGAGACAGTTTCGTTCTTGTCGCCCAGACTGGAGTGCAATGGGGC T C DTYMK Ensembl:ENSG00000168393 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4347866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13827336 Human_Splice_Rec_383280 62479 RMVar_ID_62479 Human_SNP_ID_119389802 m1A Human chr2 + 241686704 241686704 241686704 CGGCGCGGTGGCCCGCGGCGCACAGCGCTTCCACCAGCTTGCGGCTCTGCGTGCTCTTCCCGGCG CGGCGCGGTGGCCCGCGGCGCACAGCGCTTCCCCCAGCTTGCGGCTCTGCGTGCTCTTCCCGGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241686619..241686835 26863196 MeRIP-seq:(Medium) rs751863088 Functional Loss SNV dbSNP153 33..33 33 - - - 62480 RMVar_ID_62480 Human_SNP_ID_119389952 m1A Human chr2 + 241687050 241687050 241687050 CCGTGTCCCGTGCGGGCCTCCGTCCTCGGGCGAGCAGGGCCCTTCGCTCCGGGAGGGGAGGTGAC CCGTGTCCCGTGCGGGCCTCCGTCCTCGGGCGTGCAGGGCCCTTCGCTCCGGGAGGGGAGGTGAC A T NONHSAG031042.2 RNACentral:URS00008C15CA lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241687001..241687307 26863196 MeRIP-seq:(Medium) rs1033011125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4603143 62481 RMVar_ID_62481 Human_SNP_ID_119394226 m1A Human chr2 - 241701569 241701569 241701569 TGTCTGGCTCAGCGCCTTTCCCCCGGACCCCGAGCCCCCGGGGCCTCAGCCCGGCCTGAGCCGAG TGTCTGGCTCAGCGCCTTTCCCCCGGACCCCGGGCCCCCGGGGCCTCAGCCCGGCCTGAGCCGAG T C lnc-DTYMK-5 RNACentral:URS00008B20E4 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241701520..241701636 26863196 MeRIP-seq:(Medium) rs1367614812 Functional Loss SNV dbSNP153 33..33 33 - - - 62482 RMVar_ID_62482 Human_SNP_ID_119394683 m1A Human chr2 - 241702508 241702508 241702508 GACCCCGGAGCCCCCAAGGCCCGGAGCCCCGCAGCGGGCGCCAGCTCCTCCTGCAGACGGGACAG GACCCCGGAGCCCCCAAGGCCCGGAGCCCCGCGGCGGGCGCCAGCTCCTCCTGCAGACGGGACAG T C lnc-DTYMK-5 RNACentral:URS00008B20E4 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241702491..241702742 26863196 MeRIP-seq:(Medium) rs1360127115 Functional Loss SNV dbSNP153 33..33 33 - - - 62483 RMVar_ID_62483 Human_SNP_ID_119394689 m1A Human chr2 - 241702516 241702516 241702516 GAGGCCCAGACCCCGGAGCCCCCAAGGCCCGGAGCCCCGCAGCGGGCGCCAGCTCCTCCTGCAGA GAGGCCCAGACCCCGGAGCCCCCAAGGCCCGGCGCCCCGCAGCGGGCGCCAGCTCCTCCTGCAGA T G lnc-DTYMK-5 RNACentral:URS00008B20E4 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241702514..241702708 26863196 MeRIP-seq:(Medium) rs940642079 Functional Loss SNV dbSNP153 33..33 33 - - - 62484 RMVar_ID_62484 Human_SNP_ID_119394703 m1A Human chr2 - 241702541 241702541 241702541 GCGCACACGGGCGCACAGCCAGGCGGAGGCCCAGACCCCGGAGCCCCCAAGGCCCGGAGCCCCGC GCGCACACGGGCGCACAGCCAGGCGGAGGCCCGGACCCCGGAGCCCCCAAGGCCCGGAGCCCCGC T C lnc-DTYMK-5 RNACentral:URS00008B20E4 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241702534..241702741 26863196 MeRIP-seq:(Medium) rs912662467 Functional Loss SNV dbSNP153 33..33 33 - - - 62485 RMVar_ID_62485 Human_SNP_ID_119400324 m1A Human chr2 - 241721947 241721947 241721947 TCCTTGTCACTCCTTCATCCCCATCAGCTCCCACGTGGGTTTCTACACAGCAGCCTGGCAGGTGT TCCTTGTCACTCCTTCATCCCCATCAGCTCCCTCGTGGGTTTCTACACAGCAGCCTGGCAGGTGT T A lnc-DTYMK-5 RNACentral:URS00008B20E4 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241721897..241722243 26863196 MeRIP-seq:(Medium) rs112011439 Functional Loss SNV dbSNP153 33..33 33 - - - 62486 RMVar_ID_62486 Human_SNP_ID_119409775 m1A Human chr2 - 241751998 241751961 241751998 GGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGCTCC GGTCCCGGTAACAGTGACCAATGGCTCCCACT_________________________________ CAGGGGGAGCCCTCGGTCACCGTCACCGGGGCCTGGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241751671..241752224 26863196 MeRIP-seq:(Medium) rs1329566886 Functional Loss DEL dbSNP153 33..65 33 - - - 62487 RMVar_ID_62487 Human_SNP_ID_119409776 m1A Human chr2 + 241751962 241751961 241751962 GAGCCCTCGGTCACCGTCACCGGGGCCTGGGCAGGGGGAGCCCTCGGTCACCGTCACCGGGGCCT GAGCCCTCGGTCACCGTCACCGGGGCCTGGGC_GGGGGAGCCCTCGGTCACCGTCACCGGGGCCT CA C D2HGDH Ensembl:ENSG00000180902 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr2:241751734..241752175;chr2:241751793..241752096 26863196 MeRIP-seq:(Medium) rs1559382651 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_104445,RMVar_hsa_circ_16542,RMVar_hsa_circ_282654,RMVar_hsa_circ_92053,RMVar_hsa_circ_208221,RMVar_hsa_circ_208224,RMVar_hsa_circ_309249,RMVar_hsa_circ_208225 62488 RMVar_ID_62488 Human_SNP_ID_119409781 m1A Human chr2 - 241752001 241751964 241752001 CCAGGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGC CCAGGTCCCGGTAACAGTGACCAATGGCTCCC_________________________________ GGGGAGCCCTCGGTCACCGTCACCGGGGCCTGGATAGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241751839..241752095;chr2:241751739..241752208 26863196 MeRIP-seq:(Medium) rs370022160 Functional Loss DEL dbSNP153 33..65 33 - - - 62489 RMVar_ID_62489 Human_SNP_ID_119409803 m1A Human chr2 - 241752001 241751996 241752001 CCAGGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGC CCAGGTCCCGGTAACAGTGACCAATGGCTCCC_____CCAGGCCCCGGTGACGGTGACCGAGGGC GATAGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241751839..241752095;chr2:241751739..241752208 26863196 MeRIP-seq:(Medium) rs1358534775 Functional Loss DEL dbSNP153 33..37 33 - - - 62490 RMVar_ID_62490 Human_SNP_ID_119409804 m1A Human chr2 - 241751998 241751996 241751999 GGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGCTCC GGTCCCGGTAACAGTGACCAATGGCTCCCAC___CCAGGCCCCGGTGACGGTGACCGAGGGCTCC GATA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241751671..241752224 26863196 MeRIP-seq:(Medium) rs1456979140 Functional Loss DEL dbSNP153 32..34 33 - - - 62491 RMVar_ID_62491 Human_SNP_ID_119409804 m1A Human chr2 + 241751999 241751996 241751999 GAGCCCTCGGTCACCGTCACCGGGGCCTGGATAGTGGGAGCCATTGGTCACTGTTACCGGGACCT GAGCCCTCGGTCACCGTCACCGGGGCCTGG___GTGGGAGCCATTGGTCACTGTTACCGGGACCT GATA G D2HGDH Ensembl:ENSG00000180902 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:241751727..241752177;chr2:241751677..241752330 26863196 MeRIP-seq:(Medium) rs1456979140 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_13828542,Human_RBP_ID_18422631,Human_RBP_ID_18462421,Human_RBP_ID_18493979 RMVar_hsa_circ_104445,RMVar_hsa_circ_16542,RMVar_hsa_circ_282654,RMVar_hsa_circ_92053,RMVar_hsa_circ_208221,RMVar_hsa_circ_208224,RMVar_hsa_circ_309249,RMVar_hsa_circ_208225 62492 RMVar_ID_62492 Human_SNP_ID_119409806 m1A Human chr2 - 241751998 241751997 241751998 GGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGCTCC GGTCCCGGTAACAGTGACCAATGGCTCCCACTGCCCAGGCCCCGGTGACGGTGACCGAGGGCTCC AT GC - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241751671..241752224 26863196 MeRIP-seq:(Medium) rs386657188 Functional Loss MNV dbSNP153 33..34 33 - - - 62493 RMVar_ID_62493 Human_SNP_ID_119409807 m1A Human chr2 - 241751998 241751998 241751998 GGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGCTCC GGTCCCGGTAACAGTGACCAATGGCTCCCACTGTCCAGGCCCCGGTGACGGTGACCGAGGGCTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241751671..241752224 26863196 MeRIP-seq:(Medium) rs4992235 Functional Loss SNV dbSNP153 33..33 33 - - - 62494 RMVar_ID_62494 Human_SNP_ID_119409810 m1A Human chr2 - 241752001 241752001 241752001 CCAGGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGC CCAGGTCCCGGTAACAGTGACCAATGGCTCCCCCTATCCAGGCCCCGGTGACGGTGACCGAGGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241751839..241752095;chr2:241751739..241752208 26863196 MeRIP-seq:(Medium) rs866135021 Functional Loss SNV dbSNP153 33..33 33 - - - 62495 RMVar_ID_62495 Human_SNP_ID_119410040 m1A Human chr2 + 241752724 241752724 241752724 CTTGGTGGTGCGGGTGGGGACCCTCATCCCGCACTGGCTGCTTTGCTGGAGTGGCAGTCAGTCAT CTTGGTGGTGCGGGTGGGGACCCTCATCCCGCGCTGGCTGCTTTGCTGGAGTGGCAGTCAGTCAT A G D2HGDH Ensembl:ENSG00000180902 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241752716..241752938 26863196 MeRIP-seq:(Medium) rs893889588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638359,Human_RBP_ID_5132014,Human_RBP_ID_5239773,Human_RBP_ID_8110071,Human_RBP_ID_8201204,Human_RBP_ID_8728819 RMVar_hsa_circ_104445,RMVar_hsa_circ_16542,RMVar_hsa_circ_282654,RMVar_hsa_circ_92053,RMVar_hsa_circ_208221,RMVar_hsa_circ_208224,RMVar_hsa_circ_309249,RMVar_hsa_circ_208225 62496 RMVar_ID_62496 Human_SNP_ID_119410456 m1A Human chr2 - 241754145 241754145 241754145 CCGGCCGCCCCATGTGTCCCCGTGGCCACAAGATGGGCTCTACCCTTGTCTGCTCACGCCTCAGT CCGGCCGCCCCATGTGTCCCCGTGGCCACAAGGTGGGCTCTACCCTTGTCTGCTCACGCCTCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241754106..241754204 26863196 MeRIP-seq:(Medium) rs1029683110 Functional Loss SNV dbSNP153 33..33 33 - - - 62497 RMVar_ID_62497 Human_SNP_ID_119410754 m1A Human chr2 - 241755154 241755154 241755154 CGGGCCACGGGGGAGGAAGGATTCTGAGGAGGAGCAGACGGTGCTGGTGGCTGAAGCAGAACCGG CGGGCCACGGGGGAGGAAGGATTCTGAGGAGGGGCAGACGGTGCTGGTGGCTGAAGCAGAACCGG T C AC114730.2 Ensembl:ENSG00000234793 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241755114..241755232 26863196 MeRIP-seq:(Medium) rs1025973834 Functional Loss SNV dbSNP153 33..33 33 - - - 62498 RMVar_ID_62498 Human_SNP_ID_119410798 m1A Human chr2 - 241755241 241755210 241755241 CACAGGGGAGGGAAGGACATGGTGGGTGGGCCACGGGGGAGGGAAGGACACGGTGGGCGGGCCGT CACAGGGGAGGGAAGGACATGGTGGGTGGGCC_______________________________GT CGGCCCGCCCACCGTGTCCTTCCCTCCCCCGT C AC114730.2 Ensembl:ENSG00000234793 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241755194..241755343 26863196 MeRIP-seq:(Medium) rs1559388791 Functional Loss DEL dbSNP153 33..63 33 - - - 62499 RMVar_ID_62499 Human_SNP_ID_119410818 m1A Human chr2 - 241755234 241755234 241755234 GAGGGAAGGACATGGTGGGTGGGCCACGGGGGAGGGAAGGACACGGTGGGCGGGCCGTGGAGGAG GAGGGAAGGACATGGTGGGTGGGCCACGGGGGGGGGAAGGACACGGTGGGCGGGCCGTGGAGGAG T C AC114730.2 Ensembl:ENSG00000234793 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:241755132..241755318 26863196 MeRIP-seq:(Medium) rs1297059385 Functional Loss SNV dbSNP153 33..33 33 - - - 62500 RMVar_ID_62500 Human_SNP_ID_119410824 m1A Human chr2 - 241755241 241755238 241755241 CACAGGGGAGGGAAGGACATGGTGGGTGGGCCACGGGGGAGGGAAGGACACGGTGGGCGGGCCGT CACAGGGGAGGGAAGGACATGGTGGGTGGGCC___GGGGAGGGAAGGACACGGTGGGCGGGCCGT CCGT C AC114730.2 Ensembl:ENSG00000234793 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241755194..241755343 26863196 MeRIP-seq:(Medium) rs1355282457 Functional Loss DEL dbSNP153 33..35 33 - - - 62501 RMVar_ID_62501 Human_SNP_ID_119410844 m1A Human chr2 - 241755292 241755262 241755293 AGGCAGCTCAAGGGGCATGTCGGGTGGGAGGCAGGGACATGGCGGGTGGGCCACAGGGGAGGGAA AGGCAGCTCAAGGGGCATGTCGGGTGGGAGG_______________________________GAA CCCTCCCCTGTGGCCCACCCGCCATGTCCCTG C AC114730.2 Ensembl:ENSG00000234793 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:241755193..241755359 26863410 MeRIP-seq:(Medium) rs1182227106 Functional Loss DEL dbSNP153 32..62 33 - - - 62502 RMVar_ID_62502 Human_SNP_ID_119413470 m1A Human chr2 - 241763055 241763055 241763055 GTGGAGATTAAAGAGGTTCCGGGCGGGGCCCCAGGCCCTCACCCTCCCCACCCACTGCAGAAGCA GTGGAGATTAAAGAGGTTCCGGGCGGGGCCCCGGGCCCTCACCCTCCCCACCCACTGCAGAAGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241763047..241763199 26863196 MeRIP-seq:(Medium) rs985576042 Functional Loss SNV dbSNP153 33..33 33 - - - 62503 RMVar_ID_62503 Human_SNP_ID_119414281 m1A Human chr2 + 241767524 241767524 241767524 AGAGGGGGGAGAACTTGGGGAGAGAAGCAGGGAGAAGCCAAGGTAGCAGCGGCCCCAGAGGAGGG AGAGGGGGGAGAACTTGGGGAGAGAAGCAGGGGGAAGCCAAGGTAGCAGCGGCCCCAGAGGAGGG A G D2HGDH Ensembl:ENSG00000180902 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:241767471..241767718;chr2:241767470..241767917;chr2:241767460..241767802 26863196 MeRIP-seq:(Medium) rs1279285420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264497,Human_RBP_ID_5196362,Human_RBP_ID_8201219,Human_RBP_ID_9429893,Human_RBP_ID_18948868 62504 RMVar_ID_62504 Human_SNP_ID_119416655 m1A Human chr2 - 241774641 241774610 241774641 GAGCAGCCGGGAGCAGCGGGGAGCAGCCGGGGAGCAGCCGGGAGCAGCCGGGAGCAGCCGGGGCG GAGCAGCCGGGAGCAGCGGGGAGCAGCCGGGG_______________________________CG GCCCCGGCTGCTCCCGGCTGCTCCCGGCTGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241774372..241774747;chr2:241774415..241774736 26863196 MeRIP-seq:(Medium) rs1162967525 Functional Loss DEL dbSNP153 33..63 33 - - - 62505 RMVar_ID_62505 Human_SNP_ID_119416676 m1A Human chr2 - 241774641 241774631 241774642 GAGCAGCCGGGAGCAGCGGGGAGCAGCCGGGGAGCAGCCGGGAGCAGCCGGGAGCAGCCGGGGCG GAGCAGCCGGGAGCAGCGGGGAGCAGCCGGG___________AGCAGCCGGGAGCAGCCGGGGCG TCCCGGCTGCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241774372..241774747;chr2:241774415..241774736 26863196 MeRIP-seq:(Medium) rs1434694001 Functional Loss DEL dbSNP153 32..42 33 - - - 62506 RMVar_ID_62506 Human_SNP_ID_119423791 m1A Human chr2 - 241801564 241801564 241801564 TCCCAGCTGGTGGCCCGAACACAAACTCCCCCAACTGTCTCCCGTAACCATGCTCCCCCAACCCT TCCCAGCTGGTGGCCCGAACACAAACTCCCCCGACTGTCTCCCGTAACCATGCTCCCCCAACCCT T C AC131097.1 Ensembl:ENSG00000215023 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241801518..241801674 26863196 MeRIP-seq:(Medium) rs183051350 Functional Loss SNV dbSNP153 33..33 33 - - - 62507 RMVar_ID_62507 Human_SNP_ID_119423797 m1A Human chr2 - 241801578 241801578 241801578 CCCACTCCACAACCTCCCAGCTGGTGGCCCGAACACAAACTCCCCCAACTGTCTCCCGTAACCAT CCCACTCCACAACCTCCCAGCTGGTGGCCCGAGCACAAACTCCCCCAACTGTCTCCCGTAACCAT T C AC131097.1 Ensembl:ENSG00000215023 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241801492..241801634 26863196 MeRIP-seq:(Medium) rs1296885877 Functional Loss SNV dbSNP153 33..33 33 - - - 62508 RMVar_ID_62508 Human_SNP_ID_119423832 m1A Human chr2 - 241801709 241801709 241801709 GATGCCCCAACCCCCGCCCAACAGCGACCCCCAGCCCGGCAACCGCAAGGAGAGACCTCCCAACC GATGCCCCAACCCCCGCCCAACAGCGACCCCCGGCCCGGCAACCGCAAGGAGAGACCTCCCAACC T C AC131097.1 Ensembl:ENSG00000215023 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241801660..241801907 26863196 MeRIP-seq:(Medium) rs970747319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_383519 62509 RMVar_ID_62509 Human_SNP_ID_119423833 m1A Human chr2 - 241801709 241801709 241801709 GATGCCCCAACCCCCGCCCAACAGCGACCCCCAGCCCGGCAACCGCAAGGAGAGACCTCCCAACC GATGCCCCAACCCCCGCCCAACAGCGACCCCCCGCCCGGCAACCGCAAGGAGAGACCTCCCAACC T G AC131097.1 Ensembl:ENSG00000215023 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241801660..241801907 26863196 MeRIP-seq:(Medium) rs970747319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_383519 62510 RMVar_ID_62510 Human_SNP_ID_119444191 m1A Human chr2 - 241864624 241864624 241864624 CACACATTATGCACATCACACACAGCTCACACACAACACAGCACACATACCACACACACTACACA CACACATTATGCACATCACACACAGCTCACACGCAACACAGCACACATACCACACACACTACACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241864545..241864701 26863196 MeRIP-seq:(Medium) rs975451498 Functional Loss SNV dbSNP153 33..33 33 - - - 62511 RMVar_ID_62511 Human_SNP_ID_119452475 m1A Human chr2 - 241888779 241888779 241888779 AGTGAGGGGTAGTGAAGGGAAGGGAGGGAGGAAGCAGGTTGGCAGGGGAGGGGGAGCCAGTGAGA AGTGAGGGGTAGTGAAGGGAAGGGAGGGAGGAGGCAGGTTGGCAGGGGAGGGGGAGCCAGTGAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:241888735..241888824;chr2:241888739..241888867 26863196 MeRIP-seq:(Medium) rs1369835526 Functional Loss SNV dbSNP153 33..33 33 - - - 62512 RMVar_ID_62512 Human_SNP_ID_119467918 m1A Human chr2 - 241946077 241946077 241946077 ACACACGCACACACACCCACAGGCACACTCACACGCACACACACACAAACACATGCACACTTACA ACACACGCACACACACCCACAGGCACACTCACGCGCACACACACACAAACACATGCACACTTACA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241946037..241946166 26863196 MeRIP-seq:(Medium) rs200146624 Functional Loss SNV dbSNP153 33..33 33 - - - 62513 RMVar_ID_62513 Human_SNP_ID_119467919 m1A Human chr2 - 241946077 241946077 241946077 ACACACGCACACACACCCACAGGCACACTCACACGCACACACACACAAACACATGCACACTTACA ACACACGCACACACACCCACAGGCACACTCACCCGCACACACACACAAACACATGCACACTTACA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241946037..241946166 26863196 MeRIP-seq:(Medium) rs200146624 Functional Loss SNV dbSNP153 33..33 33 - - - 62514 RMVar_ID_62514 Human_SNP_ID_119468863 m1A Human chr2 + 241948768 241948768 241948768 TTGTGTGTGCGTGATGGTGTGTGAGTGACTGCATGGGTGTGATGGTGTGTGTCTGTGTGTGATTG TTGTGTGTGCGTGATGGTGTGTGAGTGACTGCGTGGGTGTGATGGTGTGTGTCTGTGTGTGATTG A G LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241948703..241948885 26863196 MeRIP-seq:(Medium) rs1174151125 Functional Loss SNV dbSNP153 33..33 33 - - - 62515 RMVar_ID_62515 Human_SNP_ID_119470253 m1A Human chr2 + 241953845 241953832 241953845 CCGGAGGTGCCCAGGCTGTGGGGAGGAGCCGGAGGTGCCCAGGCCGGGGGGAGGAGCCAGATGTG CCGGAGGTGCCCAGGCTGTG_____________GGTGCCCAGGCCGGGGGGAGGAGCCAGATGTG GGGGAGGAGCCGGA G LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241953794..241953897;chr2:241953793..241953908;chr2:241953771..241953904 26863196 MeRIP-seq:(Medium) rs1162059060 Functional Loss DEL dbSNP153 21..33 33 - - - 62516 RMVar_ID_62516 Human_SNP_ID_119471011 m1A Human chr2 + 241956625 241956625 241956625 AGTGGCAGTGGAGGGCAGGGAGAGTGGCAGGGAAGCCTGTGAGGGGCAGATGTGGAGAAGGAAGG AGTGGCAGTGGAGGGCAGGGAGAGTGGCAGGGGAGCCTGTGAGGGGCAGATGTGGAGAAGGAAGG A G LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241956587..241956877 26863196 MeRIP-seq:(Medium) rs960153205 Functional Loss SNV dbSNP153 33..33 33 - - - 62517 RMVar_ID_62517 Human_SNP_ID_119473897 m1A Human chr2 + 241968691 241968691 241968691 TTGATGATGGGTGATGGAGTGTGGGGTTGGTGACAGGTGACGGAGTGTGGGGTTGACGACGGGTG TTGATGATGGGTGATGGAGTGTGGGGTTGGTGGCAGGTGACGGAGTGTGGGGTTGACGACGGGTG A G LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241968592..241968831 26863196 MeRIP-seq:(Medium) rs150106715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5651787 62518 RMVar_ID_62518 Human_SNP_ID_119473907 m1A Human chr2 + 241968714 241968712 241968715 GGGTTGGTGACAGGTGACGGAGTGTGGGGTTGACGACGGGTGATGGAGTGTGGGGATGATGATGG GGGTTGGTGACAGGTGACGGAGTGTGGGGTT___GACGGGTGATGGAGTGTGGGGATGATGATGG TGAC T LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241968593..241968769 26863196 MeRIP-seq:(Medium) rs916706024 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5652066 62519 RMVar_ID_62519 Human_SNP_ID_119474168 m1A Human chr2 - 241969461 241969461 241969461 AACCCCAGACTCCGTCACCTGTCATCATCACCACACTCCATCATCATCCCCGCACTTCATCACCC AACCCCAGACTCCGTCACCTGTCATCATCACCCCACTCCATCATCATCCCCGCACTTCATCACCC T G lnc-PDCD1-6 RNACentral:URS00008BA079 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241969093..241969827 26863196 MeRIP-seq:(Medium) rs538536523 Functional Loss SNV dbSNP153 33..33 33 - - - 62520 RMVar_ID_62520 Human_SNP_ID_119474171 m1A Human chr2 + 241969466 241969466 241969466 ATGAAGTGCGGGGATGATGATGGAGTGTGGTGATGATGACAGGTGACGGAGTCTGGGGTTGATGA ATGAAGTGCGGGGATGATGATGGAGTGTGGTGTTGATGACAGGTGACGGAGTCTGGGGTTGATGA A T LINC01237 Ensembl:ENSG00000233806 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241969095..241969833;chr2:241969106..241969830 26863196 MeRIP-seq:(Medium) rs1239700743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638374,Human_RBP_ID_5651790,Human_RBP_ID_8203159,Human_RBP_ID_23863080 62521 RMVar_ID_62521 Human_SNP_ID_119474179 m1A Human chr2 - 241969485 241969485 241969485 TCATCAACCCCACGCCCCGTCATCAACCCCAGACTCCGTCACCTGTCATCATCACCACACTCCAT TCATCAACCCCACGCCCCGTCATCAACCCCAGGCTCCGTCACCTGTCATCATCACCACACTCCAT T C lnc-PDCD1-6 RNACentral:URS00008BA079 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr2:241969094..241969511;chr2:241969434..241969721 26863196 MeRIP-seq:(Medium) rs1037652686 Functional Loss SNV dbSNP153 33..33 33 - - - 62522 RMVar_ID_62522 Human_SNP_ID_119474254 m1A Human chr2 - 241969703 241969703 241969703 TGTCATCATCACCACACTCCATCATCATCCCCACACTTCATTACCCATCATCATCCCCACACTCC TGTCATCATCACCACACTCCATCATCATCCCCGCACTTCATTACCCATCATCATCCCCACACTCC T C lnc-PDCD1-6 RNACentral:URS00008BA079 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241969601..241969808 26863196 MeRIP-seq:(Medium) rs1341435481 Functional Loss SNV dbSNP153 33..33 33 - - - 62523 RMVar_ID_62523 Human_SNP_ID_119474569 m1A Human chr2 - 241970357 241970357 241970357 CCCACACCCCGTCATCAACCCCACACCCTGTCATTGACCCCACGCTCTGTCATAAACCCCACGCC CCCACACCCCGTCATCAACCCCACACCCTGTCGTTGACCCCACGCTCTGTCATAAACCCCACGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:241970330..241970440 26863196 MeRIP-seq:(Medium) rs1343864336 Functional Loss SNV dbSNP153 33..33 33 - - - 62524 RMVar_ID_62524 Human_SNP_ID_119507896 m1A Human chr2 + 242088510 242088510 242088510 GCGCCCCCGCGCCCCCGCGCCCCCGCGCCCCCACACCTCCACGCCCGGCACTCTGGGCGCGCGCG GCGCCCCCGCGCCCCCGCGCCCCCGCGCCCCCCCACCTCCACGCCCGGCACTCTGGGCGCGCGCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:242088373..242088584 26863196 MeRIP-seq:(Medium) rs1294132292 Functional Loss SNV dbSNP153 33..33 33 - - - 62525 RMVar_ID_62525 Human_SNP_ID_119507897 m1A Human chr2 + 242088510 242088510 242088510 GCGCCCCCGCGCCCCCGCGCCCCCGCGCCCCCACACCTCCACGCCCGGCACTCTGGGCGCGCGCG GCGCCCCCGCGCCCCCGCGCCCCCGCGCCCCCGCACCTCCACGCCCGGCACTCTGGGCGCGCGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:242088373..242088584 26863196 MeRIP-seq:(Medium) rs1294132292 Functional Loss SNV dbSNP153 33..33 33 - - - 62526 RMVar_ID_62526 Human_SNP_ID_119508029 m1A Human chr2 - 242088744 242088744 242088744 TCACCTGACGCGCCCGCGTCCCCCAGTGCCCAACGGGCGCGCCTGCCACCTGGGCCGGCACCTGA TCACCTGACGCGCCCGCGTCCCCCAGTGCCCAGCGGGCGCGCCTGCCACCTGGGCCGGCACCTGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:242088696..242089102 26863196 MeRIP-seq:(Medium) rs1438736765 Functional Loss SNV dbSNP153 33..33 33 - - - 62527 RMVar_ID_62527 Human_SNP_ID_119525047 m1A Human chr2 - 242163070 242163070 242163070 AGTGCTCGTGTTGGCCGGCAGAGCCAGCCCCCATCTCCTCTGACCTCCTCCCCACCTCTTGCCCT AGTGCTCGTGTTGGCCGGCAGAGCCAGCCCCCGTCTCCTCTGACCTCCTCCCCACCTCTTGCCCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:242163051..242163136 26863410 MeRIP-seq:(Medium) rs1217490964 Functional Loss SNV dbSNP153 33..33 33 - - - 62528 RMVar_ID_62528 Human_SNP_ID_544396680 m1A Human chr13 - 106544132 106544130 106544133 TCAGGCCGAAGAACAGTTGAGAATTGTTGAAGAACAAAGAAAGATTCATGAGGAAAGGATGAAAC TCAGGCCGAAGAACAGTTGAGAATTGTTGAA___CAAAGAAAGATTCATGAGGAAAGGATGAAAC GTTC G ARGLU1 Ensembl:ENSG00000134884 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:106544083..106544178 26863196 MeRIP-seq:(Medium) rs1209768324 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_38357,Human_RBP_ID_1480636,Human_RBP_ID_1804474,Human_RBP_ID_2370921,Human_RBP_ID_8248805,Human_RBP_ID_12095864,Human_RBP_ID_18434979,Human_RBP_ID_18527660,Human_RBP_ID_22913424,Human_RBP_ID_23113560,Human_RBP_ID_23584279,Human_RBP_ID_24543563,Human_RBP_ID_24558007,Human_RBP_ID_25031256,Human_RBP_ID_26323956,Human_RBP_ID_27807788 Human_Splice_Rec_1481858,Human_Splice_Rec_1481862,Human_Splice_Rec_1481870 62529 RMVar_ID_62529 Human_SNP_ID_544402676 m1A Human chr13 - 106567497 106567487 106567497 GGCGCGGGGCGAGGGCGTGGGGCCGGGGCGGGACGGTGCGGGCCGGGAGAATGGCGGGGACGGTC GGCGCGGGGCGAGGGCGTGGGGCCGGGGCGGG__________CCGGGAGAATGGCGGGGACGGTC GCCCGCACCGT G ARGLU1 Ensembl:ENSG00000134884 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:106567485..106567720 26863196 MeRIP-seq:(Medium) rs1178831597 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_3439071,Human_RBP_ID_8180139,Human_RBP_ID_18936165,Human_RBP_ID_19063023,Human_RBP_ID_26777958 RMVar_hsa_circ_164623 62530 RMVar_ID_62530 Human_SNP_ID_544402680 m1A Human chr13 - 106567497 106567497 106567497 GGCGCGGGGCGAGGGCGTGGGGCCGGGGCGGGACGGTGCGGGCCGGGAGAATGGCGGGGACGGTC GGCGCGGGGCGAGGGCGTGGGGCCGGGGCGGGCCGGTGCGGGCCGGGAGAATGGCGGGGACGGTC T G ARGLU1 Ensembl:ENSG00000134884 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:106567485..106567720 26863196 MeRIP-seq:(Medium) rs1372573010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439071,Human_RBP_ID_8180139,Human_RBP_ID_18936165,Human_RBP_ID_19063023,Human_RBP_ID_26777958 RMVar_hsa_circ_164623 62531 RMVar_ID_62531 Human_SNP_ID_544402728 m1A Human chr13 - 106567599 106567599 106567599 GAGAAGCAGAAGCGAGAGGAGGAGGAGAAGAAAGCGGAGTTCGAGCGGCAGCGAAAAATGTGAGT GAGAAGCAGAAGCGAGAGGAGGAGGAGAAGAAGGCGGAGTTCGAGCGGCAGCGAAAAATGTGAGT T C ARGLU1 Ensembl:ENSG00000134884 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr13:106559395..106567805;chr13:106559401..106567776 26863196 MeRIP-seq:(Medium) rs753085381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230643,Human_RBP_ID_5561049,Human_RBP_ID_24543574,Human_RBP_ID_25031471,Human_RBP_ID_26324177,Human_RBP_ID_27807795 Human_Splice_Rec_1481853,Human_Splice_Rec_1481859,Human_Splice_Rec_1481871 RMVar_hsa_circ_164623 62532 RMVar_ID_62532 Human_SNP_ID_544402750 m1A Human chr13 - 106567640 106567640 106567640 ACATCTTCGGGCGCACGGTGAGCAAGCGCAGCAGCCTGGACGAGAAGCAGAAGCGAGAGGAGGAG ACATCTTCGGGCGCACGGTGAGCAAGCGCAGCGGCCTGGACGAGAAGCAGAAGCGAGAGGAGGAG T C ARGLU1 Ensembl:ENSG00000134884 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:106567576..106567650 26863196 MeRIP-seq:(Medium) rs768443940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38377,Human_RBP_ID_3423122,Human_RBP_ID_9027077,Human_RBP_ID_24543574 Human_Splice_Rec_1481853,Human_Splice_Rec_1481859,Human_Splice_Rec_1481871 62533 RMVar_ID_62533 Human_SNP_ID_544402840 m1A Human chr13 - 106567873 106567873 106567873 GAGCCGGAGCTCGTCCCGCTCCAAGCACACCAAGAGCAGCAAGCACAACAAGAAGCGCAGCCGGT GAGCCGGAGCTCGTCCCGCTCCAAGCACACCACGAGCAGCAAGCACAACAAGAAGCGCAGCCGGT T G ARGLU1 Ensembl:ENSG00000134884 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:106567851..106567875 26863196 MeRIP-seq:(Medium) rs760846320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4262234,Human_RBP_ID_9367724,Human_RBP_ID_22919843,Human_RBP_ID_25076281,Human_RBP_ID_26324179,Human_RBP_ID_27808039 62534 RMVar_ID_62534 Human_SNP_ID_544402881 m1A Human chr13 + 106567951 106567951 106567951 TCCTTCCGGGAGACGCTCTAACCGCTCGCCTCAGGCCCCTCACGCGGCCAGTTCCCCTCGCCTCC TCCTTCCGGGAGACGCTCTAACCGCTCGCCTCGGGCCCCTCACGCGGCCAGTTCCCCTCGCCTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:106567926..106567950 26863196 MeRIP-seq:(Medium) rs1335107034 Functional Loss SNV dbSNP153 33..33 33 - - - 62535 RMVar_ID_62535 Human_SNP_ID_544818148 m1A Human chr13 - 108214803 108214803 108214803 GGGGGCAGCAAGCAGGGTGTTTGTGCAGCGGCAGGTGATGGGAGTTGCCGAGTCCACAGCGCTGT GGGGGCAGCAAGCAGGGTGTTTGTGCAGCGGCGGGTGATGGGAGTTGCCGAGTCCACAGCGCTGT T C LIG4 Ensembl:ENSG00000174405 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:108214756..108214858 26863196 MeRIP-seq:(Medium) rs1021055356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3438805,Human_RBP_ID_8075268,Human_RBP_ID_8180140,Human_RBP_ID_8940984,Human_RBP_ID_9417209,Human_RBP_ID_17833319 Human_Splice_Rec_1481936 62536 RMVar_ID_62536 Human_SNP_ID_544818149 m1A Human chr13 - 108214803 108214803 108214803 GGGGGCAGCAAGCAGGGTGTTTGTGCAGCGGCAGGTGATGGGAGTTGCCGAGTCCACAGCGCTGT GGGGGCAGCAAGCAGGGTGTTTGTGCAGCGGCCGGTGATGGGAGTTGCCGAGTCCACAGCGCTGT T G LIG4 Ensembl:ENSG00000174405 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:108214756..108214858 26863196 MeRIP-seq:(Medium) rs1021055356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3438805,Human_RBP_ID_8075268,Human_RBP_ID_8180140,Human_RBP_ID_8940984,Human_RBP_ID_9417209,Human_RBP_ID_17833319 Human_Splice_Rec_1481936 62537 RMVar_ID_62537 Human_SNP_ID_544818341 m1A Human chr13 - 108215286 108215286 108215286 TGGGGCGTCAGGCGGGGTATCTGTGGGACGTCAGGTTGGGGTCTGTAGGGCGTCACGTTGGGGGT TGGGGCGTCAGGCGGGGTATCTGTGGGACGTCGGGTTGGGGTCTGTAGGGCGTCACGTTGGGGGT T C LIG4 Ensembl:ENSG00000174405 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:108215248..108215379 26863196 MeRIP-seq:(Medium) rs1362700255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1271355,Human_RBP_ID_3439075,Human_RBP_ID_6256665,Human_RBP_ID_8180144,Human_RBP_ID_8230294,Human_RBP_ID_18936167 62538 RMVar_ID_62538 Human_SNP_ID_544818343 m1A Human chr13 - 108215300 108215300 108215300 CGGGGGAAGGTCTGTGGGGCGTCAGGCGGGGTATCTGTGGGACGTCAGGTTGGGGTCTGTAGGGC CGGGGGAAGGTCTGTGGGGCGTCAGGCGGGGTGTCTGTGGGACGTCAGGTTGGGGTCTGTAGGGC T C LIG4 Ensembl:ENSG00000174405 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:108215249..108215350 26863196 MeRIP-seq:(Medium) rs1453808192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1271355,Human_RBP_ID_3439075,Human_RBP_ID_6256665,Human_RBP_ID_8180144,Human_RBP_ID_8230294,Human_RBP_ID_18936167 62539 RMVar_ID_62539 Human_SNP_ID_544819323 m1A Human chr13 - 108218550 108218550 108218550 TTCCGTCGCTCCTCATCATCCTCCTCCAGCCCAGGGGCCGCTGCCGGCGCCACGGTCTAGCCCGG TTCCGTCGCTCCTCATCATCCTCCTCCAGCCCCGGGGCCGCTGCCGGCGCCACGGTCTAGCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr13:108218426..108229217;chr13:108218410..108218650;chr13:108218405..108218644;chr13:108218410..108218651;chr13:108218401..108218688 26863196 MeRIP-seq:(Medium) rs1462341058 Functional Loss SNV dbSNP153 33..33 33 - - - 62540 RMVar_ID_62540 Human_SNP_ID_544821888 m1A Human chr13 + 108229108 108229108 108229108 GGACTGTACCTATTACCATATTTAACAATTACATGTGGCCTAGTACCATAGTTTATTATATTGTG GGACTGTACCTATTACCATATTTAACAATTACCTGTGGCCTAGTACCATAGTTTATTATATTGTG A C ABHD13 Ensembl:ENSG00000139826 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:108229104..108229239 26863196 MeRIP-seq:(Medium) rs879234582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2371845,Human_RBP_ID_9028166 62541 RMVar_ID_62541 Human_SNP_ID_545084793 m1A Human chr13 + 109267551 109267551 109267551 GAGACAAACCCCAGCCACATCTCCAGCACACAACAACTTCCAAATGCCTGAACCGCAGTGGCCAG GAGACAAACCCCAGCCACATCTCCAGCACACATCAACTTCCAAATGCCTGAACCGCAGTGGCCAG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109267501..109267575 26863196 MeRIP-seq:(Medium) rs184939266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27426470 62542 RMVar_ID_62542 Human_SNP_ID_545084798 m1A Human chr13 - 109267567 109267567 109267567 GGTTCTGGAGGAATGTCTGGCCACTGCGGTTCAGGCATTTGGAAGTTGTTGTGTGCTGGAGATGT GGTTCTGGAGGAATGTCTGGCCACTGCGGTTCGGGCATTTGGAAGTTGTTGTGTGCTGGAGATGT T C lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:109267480..109267704 26863196 MeRIP-seq:(Medium) rs1298460170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2372688 62543 RMVar_ID_62543 Human_SNP_ID_545084803 m1A Human chr13 - 109267577 109267577 109267577 TGGGGGAGGAGGTTCTGGAGGAATGTCTGGCCACTGCGGTTCAGGCATTTGGAAGTTGTTGTGTG TGGGGGAGGAGGTTCTGGAGGAATGTCTGGCCTCTGCGGTTCAGGCATTTGGAAGTTGTTGTGTG T A lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:109267526..109267600 26863196 MeRIP-seq:(Medium) rs955258972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2372688 62544 RMVar_ID_62544 Human_SNP_ID_545084804 m1A Human chr13 - 109267577 109267577 109267577 TGGGGGAGGAGGTTCTGGAGGAATGTCTGGCCACTGCGGTTCAGGCATTTGGAAGTTGTTGTGTG TGGGGGAGGAGGTTCTGGAGGAATGTCTGGCCGCTGCGGTTCAGGCATTTGGAAGTTGTTGTGTG T C lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:109267526..109267600 26863196 MeRIP-seq:(Medium) rs955258972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2372688 62545 RMVar_ID_62545 Human_SNP_ID_545085211 m1A Human chr13 - 109269161 109269161 109269161 TTTAGGGCCTCTAAAATTATTAAAGCAGCGGCAGCTGCTGCATGCAGACATGAGGGCTAGGCTAA TTTAGGGCCTCTAAAATTATTAAAGCAGCGGCGGCTGCTGCATGCAGACATGAGGGCTAGGCTAA T C lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:109269078..109269198 26863196 MeRIP-seq:(Medium) rs1317089657 Functional Loss SNV dbSNP153 33..33 33 - - - 62546 RMVar_ID_62546 Human_SNP_ID_545085494 m1A Human chr13 - 109270153 109270153 109270153 AGAGCAGGGCATGTATGAGTAGTTGAGAACGGAGAATAGGAGTATGACTAGACGGAAAATAGTAG AGAGCAGGGCATGTATGAGTAGTTGAGAACGGTGAATAGGAGTATGACTAGACGGAAAATAGTAG T A lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109270151..109270175 26863196 MeRIP-seq:(Medium) rs1383897122 Functional Loss SNV dbSNP153 33..33 33 - - - 62547 RMVar_ID_62547 Human_SNP_ID_545125324 m1A Human chr13 - 109424252 109424252 109424252 AGATACCCCACTATGCTTAGCCCTAAACCTCAACAGTTAAATCAACAAAACTGCTCGCCAGAACA AGATACCCCACTATGCTTAGCCCTAAACCTCAGCAGTTAAATCAACAAAACTGCTCGCCAGAACA T C KR092908,AY633517,AY633517:2,AY633517:3,AY633517:4 RNACentral:URS00008EF377,RNACentral:URS0000359510,RNACentral:URS0000400AA7,RNACentral:URS000032B831,RNACentral:URS0000EE17E9 lincRNA,rRNA,rRNA,rRNA,rRNA exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1050138292 Functional Loss SNV dbSNP153 33..33 33 - - - 62548 RMVar_ID_62548 Human_SNP_ID_545125338 m1A Human chr13 - 109424309 109424309 109424309 TACGAAAGTGGCTTTAACATATCTGAACACACAATAGCTAAGACCCAAACTGGGATTAGATACCC TACGAAAGTGGCTTTAACATATCTGAACACACTATAGCTAAGACCCAAACTGGGATTAGATACCC T A KR092908 RNACentral:URS00008EF377 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:109424150..109424380 26863410 MeRIP-seq:(Medium) rs544964952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5561052,Human_RBP_ID_19829707 62549 RMVar_ID_62549 Human_SNP_ID_545216798 m1A Human chr13 + 109765539 109765539 109765539 AGCATGTAGATATCCCAGCCTCAACCACCCTGACTCCAACTCCCCACCAAGCATGTAGATATCCC AGCATGTAGATATCCCAGCCTCAACCACCCTGCCTCCAACTCCCCACCAAGCATGTAGATATCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:109765534..109765620 26863196 MeRIP-seq:(Medium) rs4773085 Functional Loss SNV dbSNP153 33..33 33 - - - 62550 RMVar_ID_62550 Human_SNP_ID_545216799 m1A Human chr13 + 109765539 109765539 109765539 AGCATGTAGATATCCCAGCCTCAACCACCCTGACTCCAACTCCCCACCAAGCATGTAGATATCCC AGCATGTAGATATCCCAGCCTCAACCACCCTGGCTCCAACTCCCCACCAAGCATGTAGATATCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:109765534..109765620 26863196 MeRIP-seq:(Medium) rs4773085 Functional Loss SNV dbSNP153 33..33 33 - - - 62551 RMVar_ID_62551 Human_SNP_ID_545216892 m1A Human chr13 - 109765936 109765936 109765936 AGGCTGGGATATCTACATGCTTGGTGGGGAGGAGGAGCCAAGGTGGATGAGGCTGGGATATCTAC AGGCTGGGATATCTACATGCTTGGTGGGGAGGTGGAGCCAAGGTGGATGAGGCTGGGATATCTAC T A IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr13:109765891..109765984;chr13:109765906..109766138 26863196 MeRIP-seq:(Medium) rs1289749177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62552 RMVar_ID_62552 Human_SNP_ID_545216893 m1A Human chr13 - 109765936 109765936 109765936 AGGCTGGGATATCTACATGCTTGGTGGGGAGGAGGAGCCAAGGTGGATGAGGCTGGGATATCTAC AGGCTGGGATATCTACATGCTTGGTGGGGAGGGGGAGCCAAGGTGGATGAGGCTGGGATATCTAC T C IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr13:109765891..109765984;chr13:109765906..109766138 26863196 MeRIP-seq:(Medium) rs1289749177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62553 RMVar_ID_62553 Human_SNP_ID_545216894 m1A Human chr13 - 109765936 109765936 109765936 AGGCTGGGATATCTACATGCTTGGTGGGGAGGAGGAGCCAAGGTGGATGAGGCTGGGATATCTAC AGGCTGGGATATCTACATGCTTGGTGGGGAGGCGGAGCCAAGGTGGATGAGGCTGGGATATCTAC T G IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr13:109765891..109765984;chr13:109765906..109766138 26863196 MeRIP-seq:(Medium) rs1289749177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62554 RMVar_ID_62554 Human_SNP_ID_545216896 m1A Human chr13 - 109765939 109765939 109765939 ATGAGGCTGGGATATCTACATGCTTGGTGGGGAGGAGGAGCCAAGGTGGATGAGGCTGGGATATC ATGAGGCTGGGATATCTACATGCTTGGTGGGGGGGAGGAGCCAAGGTGGATGAGGCTGGGATATC T C IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:109765875..109766002 26863196 MeRIP-seq:(Medium) rs1348205354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2372838 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62555 RMVar_ID_62555 Human_SNP_ID_545221077 m1A Human chr13 - 109782442 109782442 109782442 CCTGGAGGGGGCGACGAGCCGCCCACCTCCCCACGACAGTTGCAGCCGGCGCCCCCTTTGGCACC CCTGGAGGGGGCGACGAGCCGCCCACCTCCCCGCGACAGTTGCAGCCGGCGCCCCCTTTGGCACC T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109782426..109782450 26863196 MeRIP-seq:(Medium) rs376586626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62556 RMVar_ID_62556 Human_SNP_ID_545221078 m1A Human chr13 - 109782442 109782442 109782442 CCTGGAGGGGGCGACGAGCCGCCCACCTCCCCACGACAGTTGCAGCCGGCGCCCCCTTTGGCACC CCTGGAGGGGGCGACGAGCCGCCCACCTCCCCCCGACAGTTGCAGCCGGCGCCCCCTTTGGCACC T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109782426..109782450 26863196 MeRIP-seq:(Medium) rs376586626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62557 RMVar_ID_62557 Human_SNP_ID_545221409 m1A Human chr13 - 109783013 109783013 109783013 CGGCCTCCTGTCCCCCGAGGCCTCCTCCCCGTATCCGCCGTTGCCCCCGCGTCCGTCCGCGTCCC CGGCCTCCTGTCCCCCGAGGCCTCCTCCCCGTCTCCGCCGTTGCCCCCGCGTCCGTCCGCGTCCC T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:109782751..109783275 26863196 MeRIP-seq:(Medium) rs1179452995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27426490 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62558 RMVar_ID_62558 Human_SNP_ID_545221575 m1A Human chr13 - 109783356 109783356 109783356 GGCCCACGCGCCTGTCCCTGGAGGGGCTGCCCAGCCTGCCCAGCATGCACGAGTACCCACTGCCA GGCCCACGCGCCTGTCCCTGGAGGGGCTGCCCGGCCTGCCCAGCATGCACGAGTACCCACTGCCA T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109783351..109783375 26863196 MeRIP-seq:(Medium) rs775265872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6256947,Human_RBP_ID_8788226,Human_RBP_ID_9281270 Human_miRNA_ID_2794427,Human_miRNA_ID_2794893,Human_miRNA_ID_2795360 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62559 RMVar_ID_62559 Human_SNP_ID_545221714 m1A Human chr13 - 109783596 109783596 109783596 CCTACAAGGCCCCCTACACCTGTGGCGGGGACAGCGACCAGTACGTGCTCATGAGCTCCCCCGTG CCTACAAGGCCCCCTACACCTGTGGCGGGGACGGCGACCAGTACGTGCTCATGAGCTCCCCCGTG T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109783576..109783600 26863196 MeRIP-seq:(Medium) rs753030448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22040895,Human_RBP_ID_27426500 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62560 RMVar_ID_62560 Human_SNP_ID_545221715 m1A Human chr13 - 109783596 109783596 109783596 CCTACAAGGCCCCCTACACCTGTGGCGGGGACAGCGACCAGTACGTGCTCATGAGCTCCCCCGTG CCTACAAGGCCCCCTACACCTGTGGCGGGGACCGCGACCAGTACGTGCTCATGAGCTCCCCCGTG T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109783576..109783600 26863196 MeRIP-seq:(Medium) rs753030448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22040895,Human_RBP_ID_27426500 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62561 RMVar_ID_62561 Human_SNP_ID_545221833 m1A Human chr13 - 109783752 109783752 109783752 ATGGCAAGCTGCTGCCCAACGGGGACTACCTCAACGTGTCCCCCAGCGACGCGGTCACCACGGGC ATGGCAAGCTGCTGCCCAACGGGGACTACCTCGACGTGTCCCCCAGCGACGCGGTCACCACGGGC T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:109783701..109783775 26863196 MeRIP-seq:(Medium) rs1282400726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4262421,Human_RBP_ID_8788231,Human_RBP_ID_9280188 Human_miRNA_ID_1006,Human_miRNA_ID_4662,Human_miRNA_ID_8326,Human_miRNA_ID_11861,Human_miRNA_ID_15431,Human_miRNA_ID_19080,Human_miRNA_ID_22715,Human_miRNA_ID_26366,Human_miRNA_ID_1285145,Human_miRNA_ID_1305905,Human_miRNA_ID_1914635,Human_miRNA_ID_1917084,Human_miRNA_ID_1919536,Human_miRNA_ID_1921993,Human_miRNA_ID_1924448,Human_miRNA_ID_1926899,Human_miRNA_ID_1929350,Human_miRNA_ID_1931803,Human_miRNA_ID_2629631,Human_miRNA_ID_2642745,Human_miRNA_ID_2685084,Human_miRNA_ID_3125485 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62562 RMVar_ID_62562 Human_SNP_ID_545222150 m1A Human chr13 - 109784288 109784288 109784288 GACCACGCCAGCCCGGCAGCGGCCGGTGCCCCAGCCCTCCTCTGCCTCGCTGGATGAATACACCC GACCACGCCAGCCCGGCAGCGGCCGGTGCCCCCGCCCTCCTCTGCCTCGCTGGATGAATACACCC T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109784251..109784300 26863196 MeRIP-seq:(Medium) rs1311824406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8788239,Human_RBP_ID_27558407 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62563 RMVar_ID_62563 Human_SNP_ID_545222171 m1A Human chr13 - 109784337 109784337 109784337 ACGCGGCCCAGGACCTGGACCGAGGGCTGCGCAAGAGGACCTACTCCCTGACCACGCCAGCCCGG ACGCGGCCCAGGACCTGGACCGAGGGCTGCGCCAGAGGACCTACTCCCTGACCACGCCAGCCCGG T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:109784194..109784775 26863196 MeRIP-seq:(Medium) rs1334323076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8788240,Human_RBP_ID_27426509 Human_miRNA_ID_2570962,Human_miRNA_ID_3044699 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62564 RMVar_ID_62564 Human_SNP_ID_545222222 m1A Human chr13 + 109784443 109784443 109784443 GGCCTGTCCATGGTCATGTACCCGTAGAACTCACCGCCGCCGCCGCCGTCTCGGGCCGGGGGCGT GGCCTGTCCATGGTCATGTACCCGTAGAACTCCCCGCCGCCGCCGCCGTCTCGGGCCGGGGGCGT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109784426..109784450 26863196 MeRIP-seq:(Medium) rs765890903 Functional Loss SNV dbSNP153 33..33 33 - - - 62565 RMVar_ID_62565 Human_SNP_ID_545222223 m1A Human chr13 + 109784443 109784443 109784443 GGCCTGTCCATGGTCATGTACCCGTAGAACTCACCGCCGCCGCCGCCGTCTCGGGCCGGGGGCGT GGCCTGTCCATGGTCATGTACCCGTAGAACTCGCCGCCGCCGCCGCCGTCTCGGGCCGGGGGCGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109784426..109784450 26863196 MeRIP-seq:(Medium) rs765890903 Functional Loss SNV dbSNP153 33..33 33 - - - 62566 RMVar_ID_62566 Human_SNP_ID_545222288 m1A Human chr13 - 109784577 109784577 109784577 CCAGCGGCAGCGCCTCCGCCTCGGGCTCCCCCAGCGACCCCGGCTTCATGTCCCTGGACGAGTAC CCAGCGGCAGCGCCTCCGCCTCGGGCTCCCCCGGCGACCCCGGCTTCATGTCCCTGGACGAGTAC T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109784526..109784871 26863196 MeRIP-seq:(Medium) rs975536852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27426511 Human_miRNA_ID_2685085 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62567 RMVar_ID_62567 Human_SNP_ID_545222504 m1A Human chr13 - 109785074 109785071 109785074 CATCAGCGTCCCCGGCGCGCGCCGCCACCACCACCTGGTCAACCTGCCCCCCAGCCAGACGGGCC CATCAGCGTCCCCGGCGCGCGCCGCCACCACC___TGGTCAACCTGCCCCCCAGCCAGACGGGCC AGGT A IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109784876..109785175 26863196 MeRIP-seq:(Medium) rs1327493999 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_27426517 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62568 RMVar_ID_62568 Human_SNP_ID_545222677 m1A Human chr13 + 109785469 109785469 109785469 CCCTTGGGCTTCAGGTTCACCTGCCACACCTCACGGTAGGCGGCCGTGGCGGGAGCCACCAGCCC CCCTTGGGCTTCAGGTTCACCTGCCACACCTCGCGGTAGGCGGCCGTGGCGGGAGCCACCAGCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:109785419..109785519 32194978 MeRIP-seq:(Medium) rs757507101 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 62569 RMVar_ID_62569 Human_SNP_ID_545222911 m1A Human chr13 - 109785972 109785972 109785972 GCCCCAACCTCAACAACAACAACAACAACAACAACCACAGCGTGCGCAAGTGCGGCTACCTGCGC GCCCCAACCTCAACAACAACAACAACAACAACCACCACAGCGTGCGCAAGTGCGGCTACCTGCGC T G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:109785847..109786250 26863196 MeRIP-seq:(Medium) rs769951329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27429126 RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 62570 RMVar_ID_62570 Human_SNP_ID_545223129 m1A Human chr13 + 109786545 109786545 109786545 TGCTGGTGTTGCTGCTGCTGCTGCCAACGGCGACCCGGGCTCGTCGCGGTCCCCGCCGCACAGTG TGCTGGTGTTGCTGCTGCTGCTGCCAACGGCGCCCCGGGCTCGTCGCGGTCCCCGCCGCACAGTG A C AL162497.1 Ensembl:ENSG00000275741 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:109786192..109786600;chr13:109786191..109786600 26863196 MeRIP-seq:(Medium) rs1006042331 Functional Loss SNV dbSNP153 33..33 33 - - - 62571 RMVar_ID_62571 Human_SNP_ID_545316308 m1A Human chr13 - 110152401 110152401 110152401 GTGCGCCATTCATCGAGTGTCACGGCCGTGGGACCTGCAATTACTACGCAAACGCTTACAGCTTT GTGCGCCATTCATCGAGTGTCACGGCCGTGGGGCCTGCAATTACTACGCAAACGCTTACAGCTTT T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:110152351..110155375 32194978 MeRIP-seq:(Medium) rs1418118511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17685880 Human_Splice_Rec_1482419,Human_Splice_Rec_1482431,Human_Splice_Rec_1482449 RMVar_hsa_circ_124159,RMVar_hsa_circ_164696 62572 RMVar_ID_62572 Human_SNP_ID_545318681 m1A Human chr13 - 110161297 110161297 110161297 CTTCCTGTTCTGCAATATTAACAACGTGTGCAACTTTGCATCACGAAATGACTACTCGTACTGGC CTTCCTGTTCTGCAATATTAACAACGTGTGCAGCTTTGCATCACGAAATGACTACTCGTACTGGC T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:110161194..110161983 32194978 MeRIP-seq:(Medium) rs774891366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482414,Human_Splice_Rec_1482426,Human_Splice_Rec_1482444,Human_Splice_Rec_1482454 RMVar_hsa_circ_92341,RMVar_hsa_circ_164698 62573 RMVar_ID_62573 Human_SNP_ID_545321325 m1A Human chr13 + 110170654 110170654 110170654 ACCCCGGCTGTCCCTGGGGCCCCGGAGGACCCATGAATCCTTGCTCTCCTTTGGATCCAGGAATT ACCCCGGCTGTCCCTGGGGCCCCGGAGGACCCTTGAATCCTTGCTCTCCTTTGGATCCAGGAATT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110170603..110170772 26863196 MeRIP-seq:(Medium) rs965784572 Functional Loss SNV dbSNP153 33..33 33 - - - 62574 RMVar_ID_62574 Human_SNP_ID_545321818 m1A Human chr13 + 110172704 110172704 110172704 GGCAGCAGCGGTTGGTTGAAAAGGAAGAGCACAGTGAGCAAAGATTACCTTTGTCTCCTTTGGCC GGCAGCAGCGGTTGGTTGAAAAGGAAGAGCACGGTGAGCAAAGATTACCTTTGTCTCCTTTGGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110172701..110172775 26863196 MeRIP-seq:(Medium) rs774521208 Functional Loss SNV dbSNP153 33..33 33 - - - 62575 RMVar_ID_62575 Human_SNP_ID_545322278 m1A Human chr13 - 110174494 110174494 110174494 GAAGTCCTGGGCTACCTGGAGAAAAAGGTGACAAAGGCCTCCCAGGATTGGATGGCATCCCTGGT GAAGTCCTGGGCTACCTGGAGAAAAAGGTGACGAAGGCCTCCCAGGATTGGATGGCATCCCTGGT T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110174413..110174550 26863196 MeRIP-seq:(Medium) rs1566349683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482394,Human_Splice_Rec_1482395 Human_miRNA_ID_109298,Human_miRNA_ID_836702,Human_miRNA_ID_1966202,Human_miRNA_ID_2040465,Human_miRNA_ID_2361659,Human_miRNA_ID_3019445 RMVar_hsa_circ_92341,RMVar_hsa_circ_164698,RMVar_hsa_circ_102831,RMVar_hsa_circ_164699,RMVar_hsa_circ_66792,RMVar_hsa_circ_267470,RMVar_hsa_circ_267675 62576 RMVar_ID_62576 Human_SNP_ID_545322374 m1A Human chr13 - 110174735 110174735 110174735 CCTGACTTTTACTTGCAGGGAGATCAAGGGATAGCGGGTTTCCCAGGAAGCCCTGGAGAGAAGGG CCTGACTTTTACTTGCAGGGAGATCAAGGGATCGCGGGTTTCCCAGGAAGCCCTGGAGAGAAGGG T G COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110174684..110174777 26863196 MeRIP-seq:(Medium) rs1385072596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4277417,Human_RBP_ID_25031556 Human_Splice_Rec_1482392 RMVar_hsa_circ_92341,RMVar_hsa_circ_164698,RMVar_hsa_circ_102831,RMVar_hsa_circ_164699,RMVar_hsa_circ_267470,RMVar_hsa_circ_267675 62577 RMVar_ID_62577 Human_SNP_ID_545322997 m1A Human chr13 - 110176935 110176935 110176935 CGGTCTCCCTGGCAAGCCTGGCTCCATGGATAAGGTGGACATGGGCAGCATGAAGGGCCAGAAAG CGGTCTCCCTGGCAAGCCTGGCTCCATGGATAGGGTGGACATGGGCAGCATGAAGGGCCAGAAAG T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr13:110176840..110176982;chr13:110176839..110177002 26863196 MeRIP-seq:(Medium) rs1297293994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17833454 RMVar_hsa_circ_92341,RMVar_hsa_circ_164698,RMVar_hsa_circ_102831,RMVar_hsa_circ_164699,RMVar_hsa_circ_106591,RMVar_hsa_circ_68660,RMVar_hsa_circ_113039,RMVar_hsa_circ_267675,RMVar_hsa_circ_164701,RMVar_hsa_circ_81271,RMVar_hsa_circ_164703,RMVar_hsa_circ_97022,RMVar_hsa_circ_164702,RMVar_hsa_circ_164704 62578 RMVar_ID_62578 Human_SNP_ID_545323301 m1A Human chr13 + 110178083 110178083 110178083 AAAAATCACTTACCTGGAAACCCAGGAATCCCAGGAGCCCCCTGCTGTCCAGGAAGGCCAGGGAG AAAAATCACTTACCTGGAAACCCAGGAATCCCGGGAGCCCCCTGCTGTCCAGGAAGGCCAGGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110177795..110178232 26863196 MeRIP-seq:(Medium) rs760805207 Functional Loss SNV dbSNP153 33..33 33 - - - 62579 RMVar_ID_62579 Human_SNP_ID_545323319 m1A Human chr13 - 110178130 110178130 110178130 GAGATAAAGGGGCTCAAGGACTCCCTGGCATAACGGGACAGTCGGGGCTCCCTGGCCTTCCTGGA GAGATAAAGGGGCTCAAGGACTCCCTGGCATAGCGGGACAGTCGGGGCTCCCTGGCCTTCCTGGA T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110177948..110178197 26863196 MeRIP-seq:(Medium) rs756949024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17685894,Human_RBP_ID_17833455 Human_Splice_Rec_1482383 RMVar_hsa_circ_92341,RMVar_hsa_circ_164698,RMVar_hsa_circ_106591,RMVar_hsa_circ_68660,RMVar_hsa_circ_267675,RMVar_hsa_circ_81271,RMVar_hsa_circ_164703,RMVar_hsa_circ_97022,RMVar_hsa_circ_164702,RMVar_hsa_circ_164704 62580 RMVar_ID_62580 Human_SNP_ID_545323686 m1A Human chr13 + 110179320 110179320 110179320 CCAGGGGGTCCGATCGCTCCATGTTCTCCAGGAACGCCTGGTACCCCAATGCTCCCCTTCTCCCC CCAGGGGGTCCGATCGCTCCATGTTCTCCAGGGACGCCTGGTACCCCAATGCTCCCCTTCTCCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110179236..110179354 26863196 MeRIP-seq:(Medium) rs192750030 Functional Loss SNV dbSNP153 33..33 33 - - - 62581 RMVar_ID_62581 Human_SNP_ID_545327785 m1A Human chr13 + 110194961 110194961 110194961 CCCACCCCCACTTGGCTCCAAAGCCGGTAAGTATGTGGGAAAAAATCATACGCAAAGACACAACC CCCACCCCCACTTGGCTCCAAAGCCGGTAAGTCTGTGGGAAAAAATCATACGCAAAGACACAACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110194959..110195045 26863196 MeRIP-seq:(Medium) rs113190026 Functional Loss SNV dbSNP153 33..33 33 - - - 62582 RMVar_ID_62582 Human_SNP_ID_545332768 m1A Human chr13 + 110212491 110212490 110212491 GCCGTCTTGGCCAGGAATTCCCTGCAATGAAGAAAGTGAAAATGTAACCCAGGCAGAAAATCGCC GCCGTCTTGGCCAGGAATTCCCTGCAATGAAG_AAGTGAAAATGTAACCCAGGCAGAAAATCGCC GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110212489..110212559 26863196 MeRIP-seq:(Medium) rs779836221 Functional Loss DEL dbSNP153 33..33 33 - - - 62583 RMVar_ID_62583 Human_SNP_ID_545333182 m1A Human chr13 - 110213963 110213963 110213963 GTTACAAGGTGTCATTGGGTTTCCTGGAATGCAAGGACCTGAGGGGCCACAGGGACCACCAGGAC GTTACAAGGTGTCATTGGGTTTCCTGGAATGCGAGGACCTGAGGGGCCACAGGGACCACCAGGAC T C COL4A1 Ensembl:ENSG00000187498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110213926..110214025 26863196 MeRIP-seq:(Medium) rs765863981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4262632 Human_Splice_Rec_1482324,Human_Splice_Rec_1482325,Human_Splice_Rec_1482460,Human_Splice_Rec_1482461,Human_Splice_Rec_1482520,Human_Splice_Rec_1482521,Human_Splice_Rec_1482566,Human_Splice_Rec_1482567,Human_Splice_Rec_1482628,Human_Splice_Rec_1482629,Human_Splice_Rec_1482656,Human_Splice_Rec_1482657,Human_Splice_Rec_1482668,Human_Splice_Rec_1482669,Human_Splice_Rec_1482684,Human_Splice_Rec_1482685 RMVar_hsa_circ_43219,RMVar_hsa_circ_95749,RMVar_hsa_circ_164708,RMVar_hsa_circ_115936,RMVar_hsa_circ_164710 62584 RMVar_ID_62584 Human_SNP_ID_545358220 m1A Human chr13 + 110307090 110307090 110307090 TGCCCGGCGTGCGGGGGCCGCGGCGGACAGCTAGCTCTCGGAAGGCCGGACTTCCAGCGCTACGC TGCCCGGCGTGCGGGGGCCGCGGCGGACAGCTGGCTCTCGGAAGGCCGGACTTCCAGCGCTACGC A G COL4A2 Ensembl:ENSG00000134871 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:110307002..110307148 26863410 MeRIP-seq:(Medium) rs1183915508 Functional Loss SNV dbSNP153 33..33 33 - - - 62585 RMVar_ID_62585 Human_SNP_ID_545358324 m1A Human chr13 + 110307296 110307296 110307296 GGCGGGAGCGCGCGGCCCGGGAGTGTGGCTGCAGTGCGCCGGGACACCAGGGCTCCGCGCTCCGC GGCGGGAGCGCGCGGCCCGGGAGTGTGGCTGCCGTGCGCCGGGACACCAGGGCTCCGCGCTCCGC A C COL4A2 Ensembl:ENSG00000134871 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:110307271..110307590 26863196 MeRIP-seq:(Medium) rs7989823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4262653 Clinvar_Rec_229 GWAS_ID_7667 62586 RMVar_ID_62586 Human_SNP_ID_545358649 m1A Human chr13 - 110308119 110308119 110308119 AAGTCCAAGCGCGGGAGCCAGGACTTACCGCCAAGACGCTCTGGGCGAGGAACCCCACGGTCACT AAGTCCAAGCGCGGGAGCCAGGACTTACCGCCTAGACGCTCTGGGCGAGGAACCCCACGGTCACT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr13:110307827..110308166;chr13:110308051..110308125;chr13:110307851..110308125;chr13:110307817..110308125;chr13:110307301..110328430 26863196,32194978 MeRIP-seq:(Medium) rs1170159832 Functional Loss SNV dbSNP153 33..33 33 - - - 62587 RMVar_ID_62587 Human_SNP_ID_545372205 m1A Human chr13 - 110357454 110357454 110357454 AAACTTCTTCACACCCTGCAACAATAAAACACAAGGCAAAGAAAAGTTACCTAAACATTGCCAAC AAACTTCTTCACACCCTGCAACAATAAAACACGAGGCAAAGAAAAGTTACCTAAACATTGCCAAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110357451..110357575 26863196 MeRIP-seq:(Medium) rs368216378 Functional Loss SNV dbSNP153 33..33 33 - - - 62588 RMVar_ID_62588 Human_SNP_ID_545379273 m1A Human chr13 - 110385571 110385550 110385572 CACACTGTAACCACGGCCTATCCACACACTGCAGCCACGGTCTATCCACACACTGCAACCACGGC CACACTGTAACCACGGCCTATCCACACACTG______________________TGCAACCACGGC AGTGTGTGGATAGACCGTGGCTG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110385569..110385652 26863196 MeRIP-seq:(Medium) rs1277098568 Functional Loss DEL dbSNP153 32..53 33 - - - 62589 RMVar_ID_62589 Human_SNP_ID_545379392 m1A Human chr13 + 110385801 110385801 110385801 GCGTGGATAGGCCGTGGTTGCAGTGTGTGGATAGGCCGTGGTTACAGTGTGTGGATAGGCCGTGG GCGTGGATAGGCCGTGGTTGCAGTGTGTGGATGGGCCGTGGTTACAGTGTGTGGATAGGCCGTGG A G COL4A2 Ensembl:ENSG00000134871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110385800..110385915 26863196 MeRIP-seq:(Medium) rs201325420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718 62590 RMVar_ID_62590 Human_SNP_ID_545379512 m1A Human chr13 - 110385988 110385980 110385989 GCCCATCCACACGCTGTGACCACGGCCCATCCACACGCTGTGACCACGGCCCATCCACACGCTGT GCCCATCCACACGCTGTGACCACGGCCCATC_________TGACCACGGCCCATCCACACGCTGT ACAGCGTGTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110385984..110386049 26863196 MeRIP-seq:(Medium) rs1296287021 Functional Loss DEL dbSNP153 32..40 33 - - - 62591 RMVar_ID_62591 Human_SNP_ID_545381220 m1A Human chr13 - 110392351 110392351 110392351 CCTTTCTCCCTGCATCTTGGAGATAAATACCCAGTCCTCCTCCATTTACGTTTCAACTATAGCAT CCTTTCTCCCTGCATCTTGGAGATAAATACCCGGTCCTCCTCCATTTACGTTTCAACTATAGCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110392350..110392458 26863196 MeRIP-seq:(Medium) rs1392333740 Functional Loss SNV dbSNP153 33..33 33 - - - 62592 RMVar_ID_62592 Human_SNP_ID_545384758 m1A Human chr13 - 110407222 110407222 110407222 AAGCCGTTTCCTGCAGGGTTGGACTCTCCCACACCGGCTTTCCCACCCGAGGGGCGCAGTGCTGC AAGCCGTTTCCTGCAGGGTTGGACTCTCCCACGCCGGCTTTCCCACCCGAGGGGCGCAGTGCTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110407220..110407388 26863196 MeRIP-seq:(Medium) rs1443814122 Functional Loss SNV dbSNP153 33..33 33 - - - 62593 RMVar_ID_62593 Human_SNP_ID_545390332 m1A Human chr13 - 110428560 110428560 110428560 GATACTCACGGGAGGCCCGGTGAACCCCTCAGAGCCGGGGGGCCCCTGTGGACCTGAGTCTCCCT GATACTCACGGGAGGCCCGGTGAACCCCTCAGGGCCGGGGGGCCCCTGTGGACCTGAGTCTCCCT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110428551..110428600 26863196 MeRIP-seq:(Medium) rs1279465314 Functional Loss SNV dbSNP153 33..33 33 - - - 62594 RMVar_ID_62594 Human_SNP_ID_545390870 m1A Human chr13 + 110430607 110430607 110430607 CAGATGGGTCCAGTTGGAGCTCCAGGGAGACCAGTAAGTACCTGGACACAGGTGCCCACTCTGGG CAGATGGGTCCAGTTGGAGCTCCAGGGAGACCGGTAAGTACCTGGACACAGGTGCCCACTCTGGG A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr13:110430448..110430637;chr13:110430454..110430625 26863196 MeRIP-seq:(Medium) rs1221934460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482744,Human_Splice_Rec_1482745,Human_Splice_Rec_1482838,Human_Splice_Rec_1482839,Human_Splice_Rec_1482860 RMVar_hsa_circ_25503,RMVar_hsa_circ_88497,RMVar_hsa_circ_64524,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_362693,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_49849,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_266385,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724 62595 RMVar_ID_62595 Human_SNP_ID_545392346 m1A Human chr13 + 110436360 110436360 110436360 CGCGCCCACAGGAGTCACCTTCCACCCAGATCAGTACAAGGTAAAGAGCAAAATTGACTCTTTTC CGCGCCCACAGGAGTCACCTTCCACCCAGATCGGTACAAGGTAAAGAGCAAAATTGACTCTTTTC A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110436351..110436375 26863196 MeRIP-seq:(Medium) rs746705508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482750,Human_Splice_Rec_1482751,Human_Splice_Rec_1482844,Human_Splice_Rec_1482845,Human_Splice_Rec_1482861 RMVar_hsa_circ_25503,RMVar_hsa_circ_88497,RMVar_hsa_circ_64524,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_362693,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_88102,RMVar_hsa_circ_49849,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_266385,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_164731,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728 62596 RMVar_ID_62596 Human_SNP_ID_545393352 m1A Human chr13 - 110439797 110439797 110439797 TGTCCTGGTGATCCTTTTTCACCACTCAAGCCAGGGTAACCCTGGAATGAACAAAAAACAGAAGC TGTCCTGGTGATCCTTTTTCACCACTCAAGCCGGGGTAACCCTGGAATGAACAAAAAACAGAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110439776..110439850 26863196 MeRIP-seq:(Medium) rs1482261721 Functional Loss SNV dbSNP153 33..33 33 - - - 62597 RMVar_ID_62597 Human_SNP_ID_545394952 m1A Human chr13 - 110445846 110445846 110445846 GGTCCCCGGGGTCCATCAGGCCCTTGATAGCCATCCAGGCCTCGGCTTCCCTGCAAGAAAGATAT GGTCCCCGGGGTCCATCAGGCCCTTGATAGCCGTCCAGGCCTCGGCTTCCCTGCAAGAAAGATAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:110445826..110445900 26863196 MeRIP-seq:(Medium) rs1442070976 Functional Loss SNV dbSNP153 33..33 33 - - - 62598 RMVar_ID_62598 Human_SNP_ID_545394966 m1A Human chr13 + 110445881 110445881 110445881 CTATCAAGGGCCTGATGGACCCCGGGGACCCAAGGTGAGCCCGTTTCTCATGTCTTTGCCACTTA CTATCAAGGGCCTGATGGACCCCGGGGACCCATGGTGAGCCCGTTTCTCATGTCTTTGCCACTTA A T COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110445826..110445900 26863196 MeRIP-seq:(Medium) rs1355055637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482758,Human_Splice_Rec_1482759,Human_Splice_Rec_1482852,Human_Splice_Rec_1482853,Human_Splice_Rec_1482868,Human_Splice_Rec_1482869 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_362693,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_49849,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_266385,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732 62599 RMVar_ID_62599 Human_SNP_ID_545395216 m1A Human chr13 - 110446734 110446734 110446734 AGAATAGCCTTTTGGAGTTTTTGACAGTACACATATTTCCAAAGAAGAAACCCGAGCGTGGACCG AGAATAGCCTTTTGGAGTTTTTGACAGTACACGTATTTCCAAAGAAGAAACCCGAGCGTGGACCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110446732..110446875 26863196 MeRIP-seq:(Medium) rs531363913 Functional Loss SNV dbSNP153 33..33 33 - - - 62600 RMVar_ID_62600 Human_SNP_ID_545396277 m1A Human chr13 + 110450393 110450393 110450393 GGCATCCCTGCGCTCTACGGGGGCCCACCTGGACCTGATGGAAAGCGAGGGCCTCCAGGACCCCC GGCATCCCTGCGCTCTACGGGGGCCCACCTGGGCCTGATGGAAAGCGAGGGCCTCCAGGACCCCC A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110450310..110450407 26863196 MeRIP-seq:(Medium) rs772354234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482764,Human_Splice_Rec_1482765,Human_Splice_Rec_1482874,Human_Splice_Rec_1482875 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_362693,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_49849,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_15349,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732,RMVar_hsa_circ_16608 62601 RMVar_ID_62601 Human_SNP_ID_545398873 m1A Human chr13 - 110458820 110458820 110458820 GCGAAGCCCTTGGGTCCTGGCAGTCCCGGAAGACCTTTGATAGCTTCGTCGCCTTCTGTACATCT GCGAAGCCCTTGGGTCCTGGCAGTCCCGGAAGTCCTTTGATAGCTTCGTCGCCTTCTGTACATCT T A COL4A2-AS2 Ensembl:ENSG00000224821 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110458735..110458973 26863196 MeRIP-seq:(Medium) rs7327685 Functional Loss SNV dbSNP153 33..33 33 - - - 62602 RMVar_ID_62602 Human_SNP_ID_545398897 m1A Human chr13 + 110458853 110458853 110458853 CTTCCGGGACTGCCAGGACCCAAGGGCTTCGCAGGCATCAACGGGGAGCCGGGGAGGAAAGGGGA CTTCCGGGACTGCCAGGACCCAAGGGCTTCGCGGGCATCAACGGGGAGCCGGGGAGGAAAGGGGA A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110458735..110458960 26863196 MeRIP-seq:(Medium) rs765359924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482768,Human_Splice_Rec_1482769,Human_Splice_Rec_1482878 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_15349,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732,RMVar_hsa_circ_119753,RMVar_hsa_circ_16608,RMVar_hsa_circ_359949,RMVar_hsa_circ_164733 62603 RMVar_ID_62603 Human_SNP_ID_545398911 m1A Human chr13 + 110458892 110458892 110458892 AACGGGGAGCCGGGGAGGAAAGGGGACAGAGGAGACCCCGGCCAACACGGCCTCCCTGGGTTCCC AACGGGGAGCCGGGGAGGAAAGGGGACAGAGGTGACCCCGGCCAACACGGCCTCCCTGGGTTCCC A T COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110458720..110458995 26863196 MeRIP-seq:(Medium) rs1362551232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482769 Human_miRNA_ID_2690286 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_15349,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732,RMVar_hsa_circ_119753,RMVar_hsa_circ_16608,RMVar_hsa_circ_359949,RMVar_hsa_circ_164733 62604 RMVar_ID_62604 Human_SNP_ID_545399836 m1A Human chr13 - 110462324 110462324 110462324 TCGAGCCCATCGCGGCCTGGGCTGCCATCGTCACCTTTCATCCCGGGCACACCTGGGACGCCGGG TCGAGCCCATCGCGGCCTGGGCTGCCATCGTCGCCTTTCATCCCGGGCACACCTGGGACGCCGGG T C COL4A2-AS2 Ensembl:ENSG00000224821 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110462101..110462436 26863196 MeRIP-seq:(Medium) rs1407148937 Functional Loss SNV dbSNP153 33..33 33 - - - 62605 RMVar_ID_62605 Human_SNP_ID_545400687 m1A Human chr13 + 110465521 110465521 110465521 CCAGGACTGGGCCTTCCCGGCCTCAAAGGCCAACGTGGTTTCCCTGGAGACGCCGGCTTACCTGG CCAGGACTGGGCCTTCCCGGCCTCAAAGGCCAGCGTGGTTTCCCTGGAGACGCCGGCTTACCTGG A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110465401..110465575 26863196 MeRIP-seq:(Medium) rs1299794883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18434992 Human_Splice_Rec_1482775 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732,RMVar_hsa_circ_90642,RMVar_hsa_circ_119753,RMVar_hsa_circ_164733,RMVar_hsa_circ_164734 62606 RMVar_ID_62606 Human_SNP_ID_545408334 m1A Human chr13 - 110491236 110491236 110491236 CTTCTGTTCCCTTCTCTCCAAAGAATCCCTTCAGACCTGCAACCACAGACATGCTGCTTGGAACA CTTCTGTTCCCTTCTCTCCAAAGAATCCCTTCCGACCTGCAACCACAGACATGCTGCTTGGAACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110491226..110491275 26863196 MeRIP-seq:(Medium) rs760877863 Functional Loss SNV dbSNP153 33..33 33 - - - 62607 RMVar_ID_62607 Human_SNP_ID_545408338 m1A Human chr13 - 110491249 110491249 110491249 AAGCCGATGTCACCTTCTGTTCCCTTCTCTCCAAAGAATCCCTTCAGACCTGCAACCACAGACAT AAGCCGATGTCACCTTCTGTTCCCTTCTCTCCGAAGAATCCCTTCAGACCTGCAACCACAGACAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:110478072..110507483 32194978 MeRIP-seq:(Medium) rs1327728375 Functional Loss SNV dbSNP153 33..33 33 - - - 62608 RMVar_ID_62608 Human_SNP_ID_545408604 m1A Human chr13 - 110492127 110492127 110492127 CCGGCCAGCCATCATCTCCTTTGCCACCAGGCAGTCCAATCCGCCCCAGCTCTCCCTGCGACCCT CCGGCCAGCCATCATCTCCTTTGCCACCAGGCTGTCCAATCCGCCCCAGCTCTCCCTGCGACCCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110492033..110492131 26863196 MeRIP-seq:(Medium) rs942019808 Functional Loss SNV dbSNP153 33..33 33 - - - 62609 RMVar_ID_62609 Human_SNP_ID_545408605 m1A Human chr13 - 110492127 110492127 110492127 CCGGCCAGCCATCATCTCCTTTGCCACCAGGCAGTCCAATCCGCCCCAGCTCTCCCTGCGACCCT CCGGCCAGCCATCATCTCCTTTGCCACCAGGCGGTCCAATCCGCCCCAGCTCTCCCTGCGACCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110492033..110492131 26863196 MeRIP-seq:(Medium) rs942019808 Functional Loss SNV dbSNP153 33..33 33 - - - 62610 RMVar_ID_62610 Human_SNP_ID_545411637 m1A Human chr13 - 110503222 110503222 110503222 AGGCCTGCCCTGGGGCCCGGAGTCCCCGGCCCATCCTTTGGTCCCTGGGGTTCCTGGAGCTCCTG AGGCCTGCCCTGGGGCCCGGAGTCCCCGGCCCGTCCTTTGGTCCCTGGGGTTCCTGGAGCTCCTG T C COL4A2-AS1 Ensembl:ENSG00000232814 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110503179..110503300 26863196 MeRIP-seq:(Medium) rs1416541915 Functional Loss SNV dbSNP153 33..33 33 - - - 62611 RMVar_ID_62611 Human_SNP_ID_545412978 m1A Human chr13 + 110506527 110506527 110506527 CACAGCCAGACGGACCAGGAGCCCATGTGCCCAGTGGGCATGAACAAACTCTGGAGTGGATACAG CACAGCCAGACGGACCAGGAGCCCATGTGCCCGGTGGGCATGAACAAACTCTGGAGTGGATACAG A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs445348 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17685921 Human_Splice_Rec_1482817,Human_Splice_Rec_1482919,Human_Splice_Rec_1482933,Human_Splice_Rec_1482941 Clinvar_Rec_230 GWAS_ID_7668,GWAS_ID_7669,GWAS_ID_7670,GWAS_ID_7671,GWAS_ID_7672,GWAS_ID_7673,GWAS_ID_7674 RMVar_hsa_circ_109237,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_91490,RMVar_hsa_circ_164726,RMVar_hsa_circ_106872,RMVar_hsa_circ_164727,RMVar_hsa_circ_114020,RMVar_hsa_circ_164735,RMVar_hsa_circ_164736,RMVar_hsa_circ_104928,RMVar_hsa_circ_115927,RMVar_hsa_circ_126421,RMVar_hsa_circ_164739,RMVar_hsa_circ_164740 62612 RMVar_ID_62612 Human_SNP_ID_545413398 m1A Human chr13 - 110508050 110508050 110508050 TCCTCGGCCACGGGCATCATGGGCAGCGGCGCAGTGGTAGAGAGCCAGTAGGACTTGTCGTTCCG TCCTCGGCCACGGGCATCATGGGCAGCGGCGCCGTGGTAGAGAGCCAGTAGGACTTGTCGTTCCG T G COL4A2-AS1 Ensembl:ENSG00000232814 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110508000..110508094 26863196 MeRIP-seq:(Medium) rs898443428 Functional Loss SNV dbSNP153 33..33 33 - - - 62613 RMVar_ID_62613 Human_SNP_ID_545414588 m1A Human chr13 + 110512042 110512036 110512042 CACCATTCATCGAATGCAATGGAGGCCGCGGCACCTGCCACTACTACGCCAACAAGTACAGCTTC CACCATTCATCGAATGCAATGGAGGCC______CCTGCCACTACTACGCCAACAAGTACAGCTTC CGCGGCA C COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110511993..110512122 26863196 MeRIP-seq:(Medium) rs1555334194 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_27426547 RMVar_hsa_circ_109237,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_91490,RMVar_hsa_circ_164726,RMVar_hsa_circ_106872,RMVar_hsa_circ_164727,RMVar_hsa_circ_114020,RMVar_hsa_circ_164735,RMVar_hsa_circ_164736,RMVar_hsa_circ_104928,RMVar_hsa_circ_115927,RMVar_hsa_circ_126421,RMVar_hsa_circ_164739,RMVar_hsa_circ_164740 62614 RMVar_ID_62614 Human_SNP_ID_545414599 m1A Human chr13 + 110512042 110512042 110512042 CACCATTCATCGAATGCAATGGAGGCCGCGGCACCTGCCACTACTACGCCAACAAGTACAGCTTC CACCATTCATCGAATGCAATGGAGGCCGCGGCCCCTGCCACTACTACGCCAACAAGTACAGCTTC A C COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110511993..110512122 26863196 MeRIP-seq:(Medium) rs199702442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27426547 RMVar_hsa_circ_109237,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_91490,RMVar_hsa_circ_164726,RMVar_hsa_circ_106872,RMVar_hsa_circ_164727,RMVar_hsa_circ_114020,RMVar_hsa_circ_164735,RMVar_hsa_circ_164736,RMVar_hsa_circ_104928,RMVar_hsa_circ_115927,RMVar_hsa_circ_126421,RMVar_hsa_circ_164739,RMVar_hsa_circ_164740 62615 RMVar_ID_62615 Human_SNP_ID_545418088 m1A Human chr13 - 110524144 110524144 110524144 TGGGCTCCATGTACTGCCGGGGGGCGGCCGCCATCATCCTCACCTATGATGTGAATCACCGGCAG TGGGCTCCATGTACTGCCGGGGGGCGGCCGCCGTCATCCTCACCTATGATGTGAATCACCGGCAG T C RAB20 Ensembl:ENSG00000139832 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110524100..110524216 26863196 MeRIP-seq:(Medium) rs1202635606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1482960 Human_miRNA_ID_2466899 RMVar_hsa_circ_123521,RMVar_hsa_circ_164742,RMVar_hsa_circ_113850,RMVar_hsa_circ_164741 62616 RMVar_ID_62616 Human_SNP_ID_545428210 m1A Human chr13 - 110561519 110561519 110561519 GGCGCGGGGGCGCTGGGGGTTCTTACGGGAAGATGAGGAAGCCCGACAGCAAGATCGTGCTCCTG GGCGCGGGGGCGCTGGGGGTTCTTACGGGAAGGTGAGGAAGCCCGACAGCAAGATCGTGCTCCTG T C RAB20 Ensembl:ENSG00000139832 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110561414..110561652 26863196 MeRIP-seq:(Medium) rs199842595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113850,RMVar_hsa_circ_164741 62617 RMVar_ID_62617 Human_SNP_ID_545428483 m1A Human chr13 - 110561987 110561987 110561987 GGCCCCTTCGCCTCGTTCGGGCCCCGCGGCCAAGCTCCTCGCACCGCAGCCCCGGCTGTGCAGAA GGCCCCTTCGCCTCGTTCGGGCCCCGCGGCCAGGCTCCTCGCACCGCAGCCCCGGCTGTGCAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110561936..110562050 26863196 MeRIP-seq:(Medium) rs561560069 Functional Loss SNV dbSNP153 33..33 33 - - - 62618 RMVar_ID_62618 Human_SNP_ID_545428484 m1A Human chr13 - 110561987 110561987 110561987 GGCCCCTTCGCCTCGTTCGGGCCCCGCGGCCAAGCTCCTCGCACCGCAGCCCCGGCTGTGCAGAA GGCCCCTTCGCCTCGTTCGGGCCCCGCGGCCACGCTCCTCGCACCGCAGCCCCGGCTGTGCAGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110561936..110562050 26863196 MeRIP-seq:(Medium) rs561560069 Functional Loss SNV dbSNP153 33..33 33 - - - 62619 RMVar_ID_62619 Human_SNP_ID_545443079 m1A Human chr13 - 110615313 110615313 110615313 ATCGGCCCATTTTTAGGCTTGCGGCGTTATAGAAAATGATTTTGCTGGCAGGTGGAGTGCCGAGG ATCGGCCCATTTTTAGGCTTGCGGCGTTATAGCAAATGATTTTGCTGGCAGGTGGAGTGCCGAGG T G AL139385.1 Ensembl:ENSG00000275880 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110615311..110615411 26863196 MeRIP-seq:(Medium) rs893142397 Functional Loss SNV dbSNP153 33..33 33 - - - 62620 RMVar_ID_62620 Human_SNP_ID_545443231 m1A Human chr13 + 110615646 110615646 110615646 CCTCGCTGTGGGGCAATCCGGGCTTGCAGACGAGGTAAGGTCGATTCCATTTGGCCCGGGGATGG CCTCGCTGTGGGGCAATCCGGGCTTGCAGACGGGGTAAGGTCGATTCCATTTGGCCCGGGGATGG A G NAXD Ensembl:ENSG00000213995 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110615609..110616057 26863196 MeRIP-seq:(Medium) rs1053459066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276685 Human_Splice_Rec_1482961,Human_Splice_Rec_1482973 RMVar_hsa_circ_164744,RMVar_hsa_circ_90096,RMVar_hsa_circ_86464,RMVar_hsa_circ_164743 62621 RMVar_ID_62621 Human_SNP_ID_545452956 m1A Human chr13 + 110646880 110646880 110646880 CTGGGGAGCCCCTGACCCCACACCTCCTGTCCAGCTCCCAGTCCCCTGTGGCCTCTGGGGAGCCC CTGGGGAGCCCCTGACCCCACACCTCCTGTCCGGCTCCCAGTCCCCTGTGGCCTCTGGGGAGCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:110646847..110646985 26863196 MeRIP-seq:(Medium) rs528181199 Functional Loss SNV dbSNP153 33..33 33 - - - 62622 RMVar_ID_62622 Human_SNP_ID_545456933 m1A Human chr13 + 110662354 110662354 110662354 GACCCCCTTCTGCGTCATGCAACCCCATGGCCAGGCTCCGACCCCACTGCATACCATGCAACCCC GACCCCCTTCTGCGTCATGCAACCCCATGGCCGGGCTCCGACCCCACTGCATACCATGCAACCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110662345..110662518 26863196 MeRIP-seq:(Medium) rs1389246567 Functional Loss SNV dbSNP153 33..33 33 - - - 62623 RMVar_ID_62623 Human_SNP_ID_545468064 m1A Human chr13 + 110705818 110705818 110705818 CTCCCCGAGCCCAGATCCCGTTCAGCCGTGGGAAGTCTCCGCCACGATCGGCCCCCGCCCGTGCC CTCCCCGAGCCCAGATCCCGTTCAGCCGTGGGGAGTCTCCGCCACGATCGGCCCCCGCCCGTGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110705802..110706100 26863196 MeRIP-seq:(Medium) rs1463430442 Functional Loss SNV dbSNP153 33..33 33 - - - 62624 RMVar_ID_62624 Human_SNP_ID_545468200 m1A Human chr13 + 110706065 110706065 110706065 GGCCCAGCGCGGCCTGGAGCAGCGGGGGGCCCAGGCCTGGGCCGCGCGTAGTCCTCAACATGTCA GGCCCAGCGCGGCCTGGAGCAGCGGGGGGCCCCGGCCTGGGCCGCGCGTAGTCCTCAACATGTCA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr13:110705851..110706125;chr13:110706026..110706100 26863196 MeRIP-seq:(Medium) rs1326381296 Functional Loss SNV dbSNP153 33..33 33 - - - 62625 RMVar_ID_62625 Human_SNP_ID_545472970 m1A Human chr13 - 110719579 110719579 110719579 CGAGGCGCCGTCGTCGTGGTCGTGGTTGCTGGACGCGTTCTCACGGTTCTCGTTGTTGCGCTGCC CGAGGCGCCGTCGTCGTGGTCGTGGTTGCTGGGCGCGTTCTCACGGTTCTCGTTGTTGCGCTGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110719451..110719719 26863196 MeRIP-seq:(Medium) rs1342833850 Functional Loss SNV dbSNP153 33..33 33 - - - 62626 RMVar_ID_62626 Human_SNP_ID_545472984 m1A Human chr13 + 110719601 110719601 110719601 TGAGAACGCGTCCAGCAACCACGACCACGACGACGGCGCCTCGGGCACACCCAAGGAGAAGAAGG TGAGAACGCGTCCAGCAACCACGACCACGACGGCGGCGCCTCGGGCACACCCAAGGAGAAGAAGG A G ING1 Ensembl:ENSG00000153487 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:110715878..110719750;chr13:110715877..110719725 26863196 MeRIP-seq:(Medium) rs930579374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4263075 62627 RMVar_ID_62627 Human_SNP_ID_545511027 m1A Human chr13 + 110874329 110874326 110874329 TTCTCACACATTTGCACACTCACACATTGCCAACGACACACTTCCCTCCACATTCCCCCTACATT TTCTCACACATTTGCACACTCACACATTGC___CGACACACTTCCCTCCACATTCCCCCTACATT CCAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110874279..110874363 26863196 MeRIP-seq:(Medium) rs1160231603 Functional Loss DEL dbSNP153 31..33 33 - - - 62628 RMVar_ID_62628 Human_SNP_ID_545511028 m1A Human chr13 + 110874329 110874329 110874329 TTCTCACACATTTGCACACTCACACATTGCCAACGACACACTTCCCTCCACATTCCCCCTACATT TTCTCACACATTTGCACACTCACACATTGCCAGCGACACACTTCCCTCCACATTCCCCCTACATT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:110874279..110874363 26863196 MeRIP-seq:(Medium) rs1043852659 Functional Loss SNV dbSNP153 33..33 33 - - - 62629 RMVar_ID_62629 Human_SNP_ID_545517300 m1A Human chr13 - 110896097 110896097 110896097 CCTCCCCATCATGTCTGCCTTCTAGTGCCCCAAAATTATGTGAGATGCTAGAAGTTGTTTGACCT CCTCCCCATCATGTCTGCCTTCTAGTGCCCCAGAATTATGTGAGATGCTAGAAGTTGTTTGACCT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110896047..110896140 26863196 MeRIP-seq:(Medium) rs929375090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1804753,Human_RBP_ID_5246751,Human_RBP_ID_8249772,Human_RBP_ID_9028275,Human_RBP_ID_9719188,Human_RBP_ID_12098531,Human_RBP_ID_19834191,Human_RBP_ID_23585016 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 62630 RMVar_ID_62630 Human_SNP_ID_545518400 m1A Human chr13 - 110899994 110899994 110899994 TTGCCTAGGCTGGTCTCAAACTTCTGGCCTCAAGTGATCCTCCTGCTTCTGCCTCCCAAAGCGCC TTGCCTAGGCTGGTCTCAAACTTCTGGCCTCAGGTGATCCTCCTGCTTCTGCCTCCCAAAGCGCC T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9719294,Human_RBP_ID_12098775 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 62631 RMVar_ID_62631 Human_SNP_ID_545522568 m1A Human chr13 - 110914513 110914513 110914513 CGCGGCGGGGCAGCCGGGGGGCGCGGGGCGGAAGCGAGGTCGGTGGCGCCTGCGTCCGGAGGGGC CGCGGCGGGGCAGCCGGGGGGCGCGGGGCGGAGGCGAGGTCGGTGGCGCCTGCGTCCGGAGGGGC T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110914507..110914624 26863196 MeRIP-seq:(Medium) rs1243770109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260376,Human_RBP_ID_755923,Human_RBP_ID_811903,Human_RBP_ID_879030,Human_RBP_ID_5087553,Human_RBP_ID_5315538,Human_RBP_ID_5351192,Human_RBP_ID_8230152,Human_RBP_ID_17115685,Human_RBP_ID_18189365,Human_RBP_ID_18480284,Human_RBP_ID_19063298,Human_RBP_ID_22472630,Human_RBP_ID_23256177,Human_RBP_ID_26777772,Human_RBP_ID_27837127 Human_Splice_Rec_1483357 RMVar_hsa_circ_119664,RMVar_hsa_circ_164778 62632 RMVar_ID_62632 Human_SNP_ID_545522745 m1A Human chr13 + 110914847 110914847 110914847 CGAGCAGAGCGTGGCCAGGTCCCCGTCGCGGCAGGCGCGGTGCAGCGGGAAACGGAGCGAGAGCA CGAGCAGAGCGTGGCCAGGTCCCCGTCGCGGCTGGCGCGGTGCAGCGGGAAACGGAGCGAGAGCA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr13:110914801..110915050;chr13:110914800..110915010 26863196 MeRIP-seq:(Medium) rs1299705165 Functional Loss SNV dbSNP153 33..33 33 - - - 62633 RMVar_ID_62633 Human_SNP_ID_545523011 m1A Human chr13 - 110915264 110915264 110915264 TAGGCTAGACCCCGCCACCTACCGGCCGCTCCAGGCGTCCGCAGCTCCAAGCCCCGCCCTCCGCC TAGGCTAGACCCCGCCACCTACCGGCCGCTCCGGGCGTCCGCAGCTCCAAGCCCCGCCCTCCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:110915213..110915372 26863196 MeRIP-seq:(Medium) rs1243957595 Functional Loss SNV dbSNP153 33..33 33 - - - 62634 RMVar_ID_62634 Human_SNP_ID_545583490 m1A Human chr13 + 111153923 111153923 111153923 GCTCTGTATTGCAGGTCTACCCCGAGCCCCGGAGCGAGAGCGAGTGCCTGAGCAACATCCGCGAG GCTCTGTATTGCAGGTCTACCCCGAGCCCCGGGGCGAGAGCGAGTGCCTGAGCAACATCCGCGAG A G ARHGEF7 Ensembl:ENSG00000102606 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:111153689..111153990 26863196 MeRIP-seq:(Medium) rs1390499088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879589,Human_RBP_ID_4263285,Human_RBP_ID_18417815 Human_Splice_Rec_1483400,Human_Splice_Rec_1483402,Human_Splice_Rec_1483403,Human_Splice_Rec_1483472,Human_Splice_Rec_1483473,Human_Splice_Rec_1483518,Human_Splice_Rec_1483519,Human_Splice_Rec_1483560,Human_Splice_Rec_1483561,Human_Splice_Rec_1483570,Human_Splice_Rec_1483571,Human_Splice_Rec_1483600,Human_Splice_Rec_1483601,Human_Splice_Rec_1483623,Human_Splice_Rec_1483663 RMVar_hsa_circ_5360,RMVar_hsa_circ_53508,RMVar_hsa_circ_314409,RMVar_hsa_circ_348098,RMVar_hsa_circ_329608,RMVar_hsa_circ_119220,RMVar_hsa_circ_30691,RMVar_hsa_circ_164782,RMVar_hsa_circ_164783,RMVar_hsa_circ_164784 62635 RMVar_ID_62635 Human_SNP_ID_545617242 m1A Human chr13 + 111283248 111283248 111283248 GCTGCCCCACCCCTCCCACCACGGCACCCCGCACACCACCATCAACTGGGGACCCCTGGAGCCTC GCTGCCCCACCCCTCCCACCACGGCACCCCGCGCACCACCATCAACTGGGGACCCCTGGAGCCTC A G ARHGEF7 Ensembl:ENSG00000102606 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr13:111283151..111283300;chr13:111283197..111283304 26863196 MeRIP-seq:(Medium) rs1451938654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9368121,Human_RBP_ID_27807807 RMVar_hsa_circ_53508,RMVar_hsa_circ_119220,RMVar_hsa_circ_4166,RMVar_hsa_circ_113744,RMVar_hsa_circ_41966,RMVar_hsa_circ_164784,RMVar_hsa_circ_164798,RMVar_hsa_circ_81879,RMVar_hsa_circ_37650,RMVar_hsa_circ_164808,RMVar_hsa_circ_359312,RMVar_hsa_circ_122794,RMVar_hsa_circ_281390,RMVar_hsa_circ_102514,RMVar_hsa_circ_164810,RMVar_hsa_circ_164811,RMVar_hsa_circ_13285,RMVar_hsa_circ_27397,RMVar_hsa_circ_90035,RMVar_hsa_circ_164813,RMVar_hsa_circ_315291,RMVar_hsa_circ_28858,RMVar_hsa_circ_120600,RMVar_hsa_circ_164814 62636 RMVar_ID_62636 Human_SNP_ID_545617497 m1A Human chr13 - 111284110 111284110 111284110 CACACTCTCACCGCCACTCCTCATACCTCACCACCATGCACGCTCAACTGCTTATGAAAACAACT CACACTCTCACCGCCACTCCTCATACCTCACCTCCATGCACGCTCAACTGCTTATGAAAACAACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:111284105..111284250 26863196 MeRIP-seq:(Medium) rs867265107 Functional Loss SNV dbSNP153 33..33 33 - - - 62637 RMVar_ID_62637 Human_SNP_ID_545790770 m1A Human chr13 - 112063142 112063135 112063142 GGGCGAGGAGGGAGGGGAGCGCGACGGTGGGGACCGCGCGGGGGCGGGGCGGGGGTGCTGGGGAC GGGCGAGGAGGGAGGGGAGCGCGACGGTGGGG_______GGGGGCGGGGCGGGGGTGCTGGGGAC CGCGCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:112063126..112063150 26863196 MeRIP-seq:(Medium) rs1274717696 Functional Loss DEL dbSNP153 33..39 33 - - - 62638 RMVar_ID_62638 Human_SNP_ID_545790773 m1A Human chr13 - 112063142 112063137 112063142 GGGCGAGGAGGGAGGGGAGCGCGACGGTGGGGACCGCGCGGGGGCGGGGCGGGGGTGCTGGGGAC GGGCGAGGAGGGAGGGGAGCGCGACGGTGGGG_____GCGGGGGCGGGGCGGGGGTGCTGGGGAC CGCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:112063126..112063150 26863196 MeRIP-seq:(Medium) rs1198309359 Functional Loss DEL dbSNP153 33..37 33 - - - 62639 RMVar_ID_62639 Human_SNP_ID_545792351 m1A Human chr13 + 112067760 112067748 112067760 GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGAGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA GGCCCCGCCGGGGCGGGCGGC____________GGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA CGGCGGGGGCGGA C SOX1-OT,SOX1 Ensembl:ENSG00000224243,Ensembl:ENSG00000182968 lincRNA,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112067747..112067861 26863196 MeRIP-seq:(Medium) rs771858425 Functional Loss DEL dbSNP153 22..33 33 - - - 62640 RMVar_ID_62640 Human_SNP_ID_545792356 m1A Human chr13 + 112067760 112067754 112067760 GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGAGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA GGCCCCGCCGGGGCGGGCGGCGGCGGG______GGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA GGGCGGA G SOX1-OT,SOX1 Ensembl:ENSG00000224243,Ensembl:ENSG00000182968 lincRNA,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112067747..112067861 26863196 MeRIP-seq:(Medium) rs1001889852 Functional Loss DEL dbSNP153 28..33 33 - - - 62641 RMVar_ID_62641 Human_SNP_ID_545792369 m1A Human chr13 + 112067760 112067760 112067760 GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGAGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGCGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA A C SOX1-OT,SOX1 Ensembl:ENSG00000224243,Ensembl:ENSG00000182968 lincRNA,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112067747..112067861 26863196 MeRIP-seq:(Medium) rs896164603 Functional Loss SNV dbSNP153 33..33 33 - - - 62642 RMVar_ID_62642 Human_SNP_ID_545792370 m1A Human chr13 + 112067760 112067760 112067760 GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGAGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA GGCCCCGCCGGGGCGGGCGGCGGCGGGGGCGGGGGCGGGGGCGGCGGCGGCGGCGGGGGCGCCAA A G SOX1-OT,SOX1 Ensembl:ENSG00000224243,Ensembl:ENSG00000182968 lincRNA,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112067747..112067861 26863196 MeRIP-seq:(Medium) rs896164603 Functional Loss SNV dbSNP153 33..33 33 - - - 62643 RMVar_ID_62643 Human_SNP_ID_545802267 m1A Human chr13 + 112103839 112103839 112103839 GCCGTGTTTCCTGAATCCGTACGCTATGCAGGAGGGGGGCGGGGGCGGGGGCGCGGGGAGGAGGA GCCGTGTTTCCTGAATCCGTACGCTATGCAGGGGGGGGGCGGGGGCGGGGGCGCGGGGAGGAGGA A G SOX1-OT Ensembl:ENSG00000224243 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:112103826..112103875 26863196 MeRIP-seq:(Medium) rs1197828557 Functional Loss SNV dbSNP153 33..33 33 - - - 62644 RMVar_ID_62644 Human_SNP_ID_545946146 m1A Human chr13 - 112526428 112526428 112526428 GGGATGGGTGGCGACGGTGATGATGGCGTGGTAGCGGCAGTGATGGTGGTGATGATGTTGATGGT GGGATGGGTGGCGACGGTGATGATGGCGTGGTGGCGGCAGTGATGGTGGTGATGATGTTGATGGT T C TUBGCP3 Ensembl:ENSG00000126216 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112526054..112526922 26863196 MeRIP-seq:(Medium) rs1227491501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812400,Human_RBP_ID_5285433,Human_RBP_ID_5645488,Human_RBP_ID_23585454 RMVar_hsa_circ_25,RMVar_hsa_circ_126160,RMVar_hsa_circ_18363,RMVar_hsa_circ_107313,RMVar_hsa_circ_164826,RMVar_hsa_circ_315807,RMVar_hsa_circ_164827,RMVar_hsa_circ_8908,RMVar_hsa_circ_88074,RMVar_hsa_circ_272112,RMVar_hsa_circ_316485,RMVar_hsa_circ_369550,RMVar_hsa_circ_164828,RMVar_hsa_circ_28769,RMVar_hsa_circ_124860,RMVar_hsa_circ_164829,RMVar_hsa_circ_164830,RMVar_hsa_circ_306520,RMVar_hsa_circ_270137,RMVar_hsa_circ_104181,RMVar_hsa_circ_164833,RMVar_hsa_circ_26334,RMVar_hsa_circ_62541,RMVar_hsa_circ_164835,RMVar_hsa_circ_164836,RMVar_hsa_circ_164834,RMVar_hsa_circ_164832,RMVar_hsa_circ_67568,RMVar_hsa_circ_322052,RMVar_hsa_circ_326687,RMVar_hsa_circ_378601,RMVar_hsa_circ_309104,RMVar_hsa_circ_164837 62645 RMVar_ID_62645 Human_SNP_ID_545953093 m1A Human chr13 + 112553105 112553105 112553105 GTTCTTACCCACCAGCCATGCTCCTCCCCACCAGCCACACTGCCACACCACATGCCTAATCACCA GTTCTTACCCACCAGCCATGCTCCTCCCCACCCGCCACACTGCCACACCACATGCCTAATCACCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:112552801..112553350 26863196 MeRIP-seq:(Medium) rs942829703 Functional Loss SNV dbSNP153 33..33 33 - - - 62646 RMVar_ID_62646 Human_SNP_ID_545953935 m1A Human chr13 - 112556124 112556124 112556124 CTTTAACTGCAAATCAGCCTTCTTCACAAGCCACTACCTCAAAAGGTGTCCCCAGTGCTGTGTCT CTTTAACTGCAAATCAGCCTTCTTCACAAGCCGCTACCTCAAAAGGTGTCCCCAGTGCTGTGTCT T C TUBGCP3 Ensembl:ENSG00000126216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:112556076..112556178 26863196 MeRIP-seq:(Medium) rs751573665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37770,Human_RBP_ID_995606,Human_RBP_ID_17833809,Human_RBP_ID_18435014,Human_RBP_ID_18636678,Human_RBP_ID_27808053 Human_Splice_Rec_1483999,Human_Splice_Rec_1484041,Human_Splice_Rec_1484087,Human_Splice_Rec_1484137 Human_miRNA_ID_1008,Human_miRNA_ID_4664,Human_miRNA_ID_11863,Human_miRNA_ID_15433,Human_miRNA_ID_19082,Human_miRNA_ID_22717,Human_miRNA_ID_26368,Human_miRNA_ID_842128,Human_miRNA_ID_1305907,Human_miRNA_ID_1914638,Human_miRNA_ID_1917087,Human_miRNA_ID_1919539,Human_miRNA_ID_1921996,Human_miRNA_ID_1924451,Human_miRNA_ID_1926902,Human_miRNA_ID_1929353,Human_miRNA_ID_1931806,Human_miRNA_ID_2168571,Human_miRNA_ID_2170095,Human_miRNA_ID_2629634,Human_miRNA_ID_2642748,Human_miRNA_ID_3125488 RMVar_hsa_circ_88074,RMVar_hsa_circ_124860,RMVar_hsa_circ_104181,RMVar_hsa_circ_164835,RMVar_hsa_circ_164836,RMVar_hsa_circ_164834,RMVar_hsa_circ_376426,RMVar_hsa_circ_164838,RMVar_hsa_circ_342997,RMVar_hsa_circ_343366,RMVar_hsa_circ_164841,RMVar_hsa_circ_269253,RMVar_hsa_circ_164840,RMVar_hsa_circ_92845,RMVar_hsa_circ_102306,RMVar_hsa_circ_164844,RMVar_hsa_circ_83392,RMVar_hsa_circ_164845,RMVar_hsa_circ_281011,RMVar_hsa_circ_164843,RMVar_hsa_circ_121059,RMVar_hsa_circ_29327,RMVar_hsa_circ_300793,RMVar_hsa_circ_164846,RMVar_hsa_circ_357625,RMVar_hsa_circ_34657,RMVar_hsa_circ_164847,RMVar_hsa_circ_369646,RMVar_hsa_circ_47042,RMVar_hsa_circ_164848,RMVar_hsa_circ_164849,RMVar_hsa_circ_293516,RMVar_hsa_circ_164850 62647 RMVar_ID_62647 Human_SNP_ID_545960474 m1A Human chr13 + 112581821 112581821 112581821 TCACATAAATATCCCCAATCCAAATGTTTTATATACTTTTCAACTTTCTCATACCAAAAAGTTAG TCACATAAATATCCCCAATCCAAATGTTTTATGTACTTTTCAACTTTCTCATACCAAAAAGTTAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:112581819..112581924 26863196 MeRIP-seq:(Medium) rs756010770 Functional Loss SNV dbSNP153 33..33 33 - - - 62648 RMVar_ID_62648 Human_SNP_ID_545980237 m1A Human chr13 - 112657934 112657934 112657934 TGGTGTCAGGTGTCTCTATGCACATGGCAGACAGACTCCTTAGGAGGGGGAGTCCCGTCCCTACC TGGTGTCAGGTGTCTCTATGCACATGGCAGACTGACTCCTTAGGAGGGGGAGTCCCGTCCCTACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112657884..112657990 26863196 MeRIP-seq:(Medium) rs970331622 Functional Loss SNV dbSNP153 33..33 33 - - - 62649 RMVar_ID_62649 Human_SNP_ID_545982615 m1A Human chr13 - 112666139 112666138 112666140 ACAGCCTTACACACTCCCAGACTCACACATAGACACACATCCTTACACACTCCCACACACAGGCA ACAGCCTTACACACTCCCAGACTCACACATA__CACACATCCTTACACACTCCCACACACAGGCA GTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112666088..112666193 26863196 MeRIP-seq:(Medium) rs1555350380 Functional Loss DEL dbSNP153 32..33 33 - - - 62650 RMVar_ID_62650 Human_SNP_ID_545982616 m1A Human chr13 - 112666139 112666139 112666139 ACAGCCTTACACACTCCCAGACTCACACATAGACACACATCCTTACACACTCCCACACACAGGCA ACAGCCTTACACACTCCCAGACTCACACATAGCCACACATCCTTACACACTCCCACACACAGGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112666088..112666193 26863196 MeRIP-seq:(Medium) rs1186973640 Functional Loss SNV dbSNP153 33..33 33 - - - 62651 RMVar_ID_62651 Human_SNP_ID_545989963 m1A Human chr13 + 112690085 112690085 112690085 GGGGAGGAGGAGACTCGGGAGGAGCAGAGCGCAGGCTCCGCCGCGGCCGGGGTGCTCCAGCCGAG GGGGAGGAGGAGACTCGGGAGGAGCAGAGCGCCGGCTCCGCCGCGGCCGGGGTGCTCCAGCCGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:112689942..112697093;chr13:112689997..112690501 26863196 MeRIP-seq:(Medium) rs1345017525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18435020 62652 RMVar_ID_62652 Human_SNP_ID_545996888 m1A Human chr13 + 112714039 112714039 112714039 CCCCCCCACCCCTGATCCCACACCTCCCTTTCACTCCCCCGACCCCTGATCCCACGCCTCCCTTC CCCCCCCACCCCTGATCCCACACCTCCCTTTCCCTCCCCCGACCCCTGATCCCACGCCTCCCTTC A C ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:112713985..112714172 26863196 MeRIP-seq:(Medium) rs1469185235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439132,Human_RBP_ID_5127374,Human_RBP_ID_17075969,Human_RBP_ID_18936179 62653 RMVar_ID_62653 Human_SNP_ID_546004746 m1A Human chr13 + 112741207 112741207 112741207 GTTTTTTTGGGAGGCTGGGGACTGGGGAGGTGAGGGACATGGAGCTGTAGTCGGGAGGGTTGGGC GTTTTTTTGGGAGGCTGGGGACTGGGGAGGTGTGGGACATGGAGCTGTAGTCGGGAGGGTTGGGC A T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:112741205..112741421 26863196 MeRIP-seq:(Medium) rs1489121707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8180180,Human_RBP_ID_26777991 62654 RMVar_ID_62654 Human_SNP_ID_546010914 m1A Human chr13 + 112763273 112763273 112763273 CATCTTGGCCAAGGGGACCCCAAGGAAATGGGAAAGGCGAGTTCAGGCTCTGATGGGAAGAGGGG CATCTTGGCCAAGGGGACCCCAAGGAAATGGGGAAGGCGAGTTCAGGCTCTGATGGGAAGAGGGG A G ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:112763270..112763370 32194978 MeRIP-seq:(Medium) rs1432891737 Functional Loss SNV dbSNP153 33..33 33 - - - 62655 RMVar_ID_62655 Human_SNP_ID_546011683 m1A Human chr13 + 112765906 112765906 112765906 TCCCCTCACAGCGCTGAGCAGGCGTAACCGCCAGGGTCCTCCCCCTTCTGAAGCCGCGGCTTCCT TCCCCTCACAGCGCTGAGCAGGCGTAACCGCCGGGGTCCTCCCCCTTCTGAAGCCGCGGCTTCCT A G ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:112765905..112766067 32194978 MeRIP-seq:(Medium) rs1005188769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439191 62656 RMVar_ID_62656 Human_SNP_ID_546015697 m1A Human chr13 + 112778700 112778682 112778701 AGTAGCCACTGGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG AGTAGCCACTGGAGT___________________GAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG TGAGTAGCCGCTGGAGTGAG T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112778683..112778940 26863196 MeRIP-seq:(Medium) rs1290014220 Functional Loss DEL dbSNP153 16..34 33 - - - 62657 RMVar_ID_62657 Human_SNP_ID_546015704 m1A Human chr13 + 112778700 112778698 112778701 AGTAGCCACTGGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG AGTAGCCACTGGAGTGAGTAGCCGCTGGAGT___GAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG TGAG T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112778683..112778940 26863196 MeRIP-seq:(Medium) rs1195092818 Functional Loss DEL dbSNP153 32..34 33 - - - 62658 RMVar_ID_62658 Human_SNP_ID_546015705 m1A Human chr13 + 112778700 112778698 112778700 AGTAGCCACTGGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG AGTAGCCACTGGAGTGAGTAGCCGCTGGAGT__GGAGTAGCCGCTGGAGTGAGTAGCCGCTGGAG TGA T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112778683..112778940 26863196 MeRIP-seq:(Medium) rs1286795590 Functional Loss DEL dbSNP153 32..33 33 - - - 62659 RMVar_ID_62659 Human_SNP_ID_546015718 m1A Human chr13 + 112778745 112778745 112778745 GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCACTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCCCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG A C ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112778520..112778799 26863196 MeRIP-seq:(Medium) rs61961155 Functional Loss SNV dbSNP153 33..33 33 - - - 62660 RMVar_ID_62660 Human_SNP_ID_546015719 m1A Human chr13 + 112778745 112778745 112778745 GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCACTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG A G ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112778520..112778799 26863196 MeRIP-seq:(Medium) rs61961155 Functional Loss SNV dbSNP153 33..33 33 - - - 62661 RMVar_ID_62661 Human_SNP_ID_546015948 m1A Human chr13 + 112779312 112779294 112779313 AGTAGCCACTGGGGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTG AGTAGCCACTGGGGT___________________GAGTAGCCGCTGGAGTGAGGAGTAGCCGCTG TGAGTAGCCGCTGGAGTGAG T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112778867..112779474 26863196 MeRIP-seq:(Medium) rs1284118974 Functional Loss DEL dbSNP153 16..34 33 - - - 62662 RMVar_ID_62662 Human_SNP_ID_546015953 m1A Human chr13 + 112779312 112779310 112779313 AGTAGCCACTGGGGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTG AGTAGCCACTGGGGTGAGTAGCCGCTGGAGT___GAGTAGCCGCTGGAGTGAGGAGTAGCCGCTG TGAG T ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112778867..112779474 26863196 MeRIP-seq:(Medium) rs1325586920 Functional Loss DEL dbSNP153 32..34 33 - - - 62663 RMVar_ID_62663 Human_SNP_ID_546034646 m1A Human chr13 + 112840337 112840337 112840337 CCTCAGCCTCCCCACTCTCCCGTGCCCTCCAGACTCAGCCTCCCCACTCTCCCGTGCCTTCCAGC CCTCAGCCTCCCCACTCTCCCGTGCCCTCCAGCCTCAGCCTCCCCACTCTCCCGTGCCTTCCAGC A C ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112840334..112840424 26863196 MeRIP-seq:(Medium) rs111173909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17075996,Human_RBP_ID_18936206 RMVar_hsa_circ_728,RMVar_hsa_circ_22313,RMVar_hsa_circ_113720,RMVar_hsa_circ_117988,RMVar_hsa_circ_97642,RMVar_hsa_circ_164852,RMVar_hsa_circ_164854,RMVar_hsa_circ_164855,RMVar_hsa_circ_164853,RMVar_hsa_circ_340125,RMVar_hsa_circ_15331,RMVar_hsa_circ_117979,RMVar_hsa_circ_355226,RMVar_hsa_circ_78946,RMVar_hsa_circ_86515,RMVar_hsa_circ_164860,RMVar_hsa_circ_164861,RMVar_hsa_circ_164862,RMVar_hsa_circ_164864,RMVar_hsa_circ_119377,RMVar_hsa_circ_164865,RMVar_hsa_circ_76950,RMVar_hsa_circ_102817,RMVar_hsa_circ_164866,RMVar_hsa_circ_319862,RMVar_hsa_circ_164868,RMVar_hsa_circ_83674,RMVar_hsa_circ_77595,RMVar_hsa_circ_164869,RMVar_hsa_circ_269352,RMVar_hsa_circ_164870 62664 RMVar_ID_62664 Human_SNP_ID_546040840 m1A Human chr13 + 112860356 112860356 112860356 TCAGCTTCACCTCCCTCCCCATCCTCCTGTACAGCCTCATGGAGCAGCATGTTGGCATTGACGTG TCAGCTTCACCTCCCTCCCCATCCTCCTGTACGGCCTCATGGAGCAGCATGTTGGCATTGACGTG A G ATP11A Ensembl:ENSG00000068650 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:112860271..112860425 26863196 MeRIP-seq:(Medium) rs1566583799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37388,Human_RBP_ID_879261,Human_RBP_ID_2374795,Human_RBP_ID_18936520,Human_RBP_ID_26324204 Human_Splice_Rec_1484204,Human_Splice_Rec_1484205,Human_Splice_Rec_1484262,Human_Splice_Rec_1484263,Human_Splice_Rec_1484320,Human_Splice_Rec_1484321,Human_Splice_Rec_1484380,Human_Splice_Rec_1484424 RMVar_hsa_circ_117988,RMVar_hsa_circ_97642,RMVar_hsa_circ_164852,RMVar_hsa_circ_164853,RMVar_hsa_circ_15331,RMVar_hsa_circ_65235,RMVar_hsa_circ_117979,RMVar_hsa_circ_78946,RMVar_hsa_circ_86515,RMVar_hsa_circ_164861,RMVar_hsa_circ_164862,RMVar_hsa_circ_164864,RMVar_hsa_circ_119377,RMVar_hsa_circ_164865,RMVar_hsa_circ_76950,RMVar_hsa_circ_102817,RMVar_hsa_circ_164866,RMVar_hsa_circ_164868,RMVar_hsa_circ_83674,RMVar_hsa_circ_77595,RMVar_hsa_circ_164869,RMVar_hsa_circ_269352,RMVar_hsa_circ_73365,RMVar_hsa_circ_164870,RMVar_hsa_circ_39777,RMVar_hsa_circ_359987,RMVar_hsa_circ_28090,RMVar_hsa_circ_164872,RMVar_hsa_circ_73681,RMVar_hsa_circ_122613,RMVar_hsa_circ_164873,RMVar_hsa_circ_69032,RMVar_hsa_circ_371339,RMVar_hsa_circ_307513,RMVar_hsa_circ_164874 62665 RMVar_ID_62665 Human_SNP_ID_546047931 m1A Human chr13 - 112881912 112881912 112881912 GAGTGTCACCTGCTGAGAGTGGGAGCTGTACCAGGCGGCCGAGGGACAGGTGCTCTGGTAGCCTG GAGTGTCACCTGCTGAGAGTGGGAGCTGTACCGGGCGGCCGAGGGACAGGTGCTCTGGTAGCCTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112881860..112881973 26863196 MeRIP-seq:(Medium) rs575398896 Functional Loss SNV dbSNP153 33..33 33 - - - 62666 RMVar_ID_62666 Human_SNP_ID_546047932 m1A Human chr13 - 112881912 112881912 112881912 GAGTGTCACCTGCTGAGAGTGGGAGCTGTACCAGGCGGCCGAGGGACAGGTGCTCTGGTAGCCTG GAGTGTCACCTGCTGAGAGTGGGAGCTGTACCCGGCGGCCGAGGGACAGGTGCTCTGGTAGCCTG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:112881860..112881973 26863196 MeRIP-seq:(Medium) rs575398896 Functional Loss SNV dbSNP153 33..33 33 - - - 62667 RMVar_ID_62667 Human_SNP_ID_546047980 m1A Human chr13 + 112882000 112882000 112882000 CACGGAGCCCCCACCCATCCTCGGCGGTTCCCATCACCACTGCAGTTCCATCCCAAGTCACAGCT CACGGAGCCCCCACCCATCCTCGGCGGTTCCCGTCACCACTGCAGTTCCATCCCAAGTCACAGCT A G ATP11A Ensembl:ENSG00000068650 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:112881950..112882050 26863196 MeRIP-seq:(Medium) rs1460093435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27426682 RMVar_hsa_circ_269352,RMVar_hsa_circ_267495 62668 RMVar_ID_62668 Human_SNP_ID_546048309 m1A Human chr13 + 112882972 112882949 112882973 AGCACCGCACCTCTGCCCGCCTCCCGCACTGCAGCTCCGCCCGCCGGGCTCTGCGTCCCCACGTC AGCACCGCAC________________________CTCCGCCCGCCGGGCTCTGCGTCCCCACGTC CCTCTGCCCGCCTCCCGCACTGCAG C ATP11A Ensembl:ENSG00000068650 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112882921..112883175 26863196 MeRIP-seq:(Medium) rs1420521434 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_17076002,Human_RBP_ID_27426710 Human_miRNA_ID_631861 RMVar_hsa_circ_269352,RMVar_hsa_circ_267495 62669 RMVar_ID_62669 Human_SNP_ID_546048322 m1A Human chr13 + 112882972 112882972 112882972 AGCACCGCACCTCTGCCCGCCTCCCGCACTGCAGCTCCGCCCGCCGGGCTCTGCGTCCCCACGTC AGCACCGCACCTCTGCCCGCCTCCCGCACTGCGGCTCCGCCCGCCGGGCTCTGCGTCCCCACGTC A G ATP11A Ensembl:ENSG00000068650 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112882921..112883175 26863196 MeRIP-seq:(Medium) rs562263238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17076002,Human_RBP_ID_27426710 Human_miRNA_ID_631861 RMVar_hsa_circ_269352,RMVar_hsa_circ_267495 62670 RMVar_ID_62670 Human_SNP_ID_546048379 m1A Human chr13 + 112883068 112883060 112883068 GTCACCTCGTCCCCACATCCCCTTGCCCCGTCACCTCGTCCTCATGTCCCCTTGTCCTGTCACCT GTCACCTCGTCCCCACATCCCCTTG________CCTCGTCCTCATGTCCCCTTGTCCTGTCACCT GCCCCGTCA G ATP11A Ensembl:ENSG00000068650 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:112882876..112883122 26863196 MeRIP-seq:(Medium) rs982679562 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_3439718,Human_RBP_ID_4263627,Human_RBP_ID_5127412,Human_RBP_ID_17076005,Human_RBP_ID_17562146,Human_RBP_ID_17651043,Human_RBP_ID_18936209 RMVar_hsa_circ_269352,RMVar_hsa_circ_267495 62671 RMVar_ID_62671 Human_SNP_ID_546048385 m1A Human chr13 + 112883068 112883068 112883068 GTCACCTCGTCCCCACATCCCCTTGCCCCGTCACCTCGTCCTCATGTCCCCTTGTCCTGTCACCT GTCACCTCGTCCCCACATCCCCTTGCCCCGTCGCCTCGTCCTCATGTCCCCTTGTCCTGTCACCT A G ATP11A Ensembl:ENSG00000068650 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:112882876..112883122 26863196 MeRIP-seq:(Medium) rs1290980144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439718,Human_RBP_ID_4263627,Human_RBP_ID_5127412,Human_RBP_ID_17076005,Human_RBP_ID_17562146,Human_RBP_ID_17651043,Human_RBP_ID_18936209 RMVar_hsa_circ_269352,RMVar_hsa_circ_267495 62672 RMVar_ID_62672 Human_SNP_ID_546096536 m1A Human chr13 + 113050742 113050730 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGG____________GCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GGGGGCGGGGGGA G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1204906208 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62673 RMVar_ID_62673 Human_SNP_ID_546096540 m1A Human chr13 + 113050742 113050734 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGG________GCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCGGGGGGA G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1249981278 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62674 RMVar_ID_62674 Human_SNP_ID_546096548 m1A Human chr13 + 113050742 113050739 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGG___GCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GGGA G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1183470919 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62675 RMVar_ID_62675 Human_SNP_ID_546096550 m1A Human chr13 + 113050742 113050740 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGG__GCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GGA G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1413676333 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62676 RMVar_ID_62676 Human_SNP_ID_546096554 m1A Human chr13 + 113050742 113050741 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGG_GCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GA G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1422177657 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62677 RMVar_ID_62677 Human_SNP_ID_546096556 m1A Human chr13 - 113050764 113050742 113050765 CCACCGCCCCCTGCCGCCCCCCTCCCCCCGCCACCGCCCCCCGCACCCCCCCGCTCCCCCCGCCC CCACCGCCCCCTGCCGCCCCCCTCCCCCCGC_______________________TCCCCCCGCCC AGCGGGGGGGTGCGGGGGGCGGTG A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113050633..113050775 26863196 MeRIP-seq:(Medium) rs1298294222 Functional Loss DEL dbSNP153 32..54 33 - - - 62678 RMVar_ID_62678 Human_SNP_ID_546096559 m1A Human chr13 + 113050742 113050742 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGCGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA A C MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1462472774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62679 RMVar_ID_62679 Human_SNP_ID_546096560 m1A Human chr13 + 113050742 113050742 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA A G MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1462472774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62680 RMVar_ID_62680 Human_SNP_ID_546096561 m1A Human chr13 + 113050742 113050742 113050742 GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGAGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA GCAGGGGGGGCGGGGGCGGGGGGGGCGGGGGGTGCGGGGGGGTGCGGGGGGCGGTGGCGGGGGGA A T MCF2L Ensembl:ENSG00000126217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113050691..113050775 26863196 MeRIP-seq:(Medium) rs1462472774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494 62681 RMVar_ID_62681 Human_SNP_ID_546096585 m1A Human chr13 - 113050764 113050757 113050764 CCACCGCCCCCTGCCGCCCCCCTCCCCCCGCCACCGCCCCCCGCACCCCCCCGCTCCCCCCGCCC CCACCGCCCCCTGCCGCCCCCCTCCCCCCGCC_______CCCGCACCCCCCCGCTCCCCCCGCCC GGGGCGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113050633..113050775 26863196 MeRIP-seq:(Medium) rs1372137875 Functional Loss DEL dbSNP153 33..39 33 - - - 62682 RMVar_ID_62682 Human_SNP_ID_546096590 m1A Human chr13 - 113050764 113050764 113050764 CCACCGCCCCCTGCCGCCCCCCTCCCCCCGCCACCGCCCCCCGCACCCCCCCGCTCCCCCCGCCC CCACCGCCCCCTGCCGCCCCCCTCCCCCCGCCCCCGCCCCCCGCACCCCCCCGCTCCCCCCGCCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113050633..113050775 26863196 MeRIP-seq:(Medium) rs1376874628 Functional Loss SNV dbSNP153 33..33 33 - - - 62683 RMVar_ID_62683 Human_SNP_ID_546098429 m1A Human chr13 - 113057193 113057141 113057193 CCCAAACACACAGCACCTAAACACTCAGCACCAAAACACACAGCACCTACTCAGCACCCAAACAT CCCAAACACACAGCACCTAAACACTCAGCACC_________________________________ GGGTGCTGAGTGGGTGCTGAATGTTTGGGTGCTGAGTAGGTGCTGTGTGTTTT G HSALNG0099551 RNACentral:URS0000EA4812 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113057171..113057284 26863196 MeRIP-seq:(Medium) rs1566815135 Functional Loss DEL dbSNP153 33..65 33 - - - 62684 RMVar_ID_62684 Human_SNP_ID_546098447 m1A Human chr13 - 113057193 113057178 113057193 CCCAAACACACAGCACCTAAACACTCAGCACCAAAACACACAGCACCTACTCAGCACCCAAACAT CCCAAACACACAGCACCTAAACACTCAGCACC_______________TACTCAGCACCCAAACAT AGGTGCTGTGTGTTTT A HSALNG0099551 RNACentral:URS0000EA4812 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113057171..113057284 26863196 MeRIP-seq:(Medium) rs1318437724 Functional Loss DEL dbSNP153 33..47 33 - - - 62685 RMVar_ID_62685 Human_SNP_ID_546098452 m1A Human chr13 - 113057193 113057193 113057193 CCCAAACACACAGCACCTAAACACTCAGCACCAAAACACACAGCACCTACTCAGCACCCAAACAT CCCAAACACACAGCACCTAAACACTCAGCACCCAAACACACAGCACCTACTCAGCACCCAAACAT T G HSALNG0099551 RNACentral:URS0000EA4812 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113057171..113057284 26863196 MeRIP-seq:(Medium) rs1319558560 Functional Loss SNV dbSNP153 33..33 33 - - - 62686 RMVar_ID_62686 Human_SNP_ID_546101159 m1A Human chr13 + 113065078 113065078 113065078 AGTGCTGTGTGCGCACACAGAGAAGAAGGACAAGGCGAAGGTACATGGGGGGTGCTCCGGCTGGA AGTGCTGTGTGCGCACACAGAGAAGAAGGACAGGGCGAAGGTACATGGGGGGTGCTCCGGCTGGA A G MCF2L Ensembl:ENSG00000126217 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113064919..113065135 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18979019 Human_Splice_Rec_1484491,Human_Splice_Rec_1484553,Human_Splice_Rec_1484607,Human_Splice_Rec_1484665,Human_Splice_Rec_1484733,Human_Splice_Rec_1484791,Human_Splice_Rec_1484869,Human_Splice_Rec_1484875 RMVar_hsa_circ_74134,RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_53494,RMVar_hsa_circ_320433,RMVar_hsa_circ_164879,RMVar_hsa_circ_164877,RMVar_hsa_circ_164878,RMVar_hsa_circ_84652 62687 RMVar_ID_62687 Human_SNP_ID_546105039 m1A Human chr13 - 113079810 113079808 113079810 TCTCCTCTGCCTGGACCCTCCTCCATTCAGACATTCCTCTGCCTGGACCCTCCTCCGTGCAGACG TCTCCTCTGCCTGGACCCTCCTCCATTCAGAC__TCCTCTGCCTGGACCCTCCTCCGTGCAGACG AAT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113079803..113079942 26863196 MeRIP-seq:(Medium) rs1233162668 Functional Loss DEL dbSNP153 33..34 33 - - - 62688 RMVar_ID_62688 Human_SNP_ID_546105045 m1A Human chr13 - 113079810 113079810 113079810 TCTCCTCTGCCTGGACCCTCCTCCATTCAGACATTCCTCTGCCTGGACCCTCCTCCGTGCAGACG TCTCCTCTGCCTGGACCCTCCTCCATTCAGACGTTCCTCTGCCTGGACCCTCCTCCGTGCAGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113079803..113079942 26863196 MeRIP-seq:(Medium) rs79099872 Functional Loss SNV dbSNP153 33..33 33 - - - 62689 RMVar_ID_62689 Human_SNP_ID_546106407 m1A Human chr13 - 113084249 113084249 113084249 TTTTCTGGGGTTCAGGAGGTTTTCTGGGGTTCAGGAGGTTCTGGGGGTTCAGGAGGTTCTAGGGG TTTTCTGGGGTTCAGGAGGTTTTCTGGGGTTCGGGAGGTTCTGGGGGTTCAGGAGGTTCTAGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113084237..113084384 26863196 MeRIP-seq:(Medium) rs1190651349 Functional Loss SNV dbSNP153 33..33 33 - - - 62690 RMVar_ID_62690 Human_SNP_ID_546136741 m1A Human chr13 - 113184879 113184879 113184879 AAGCACGGGCTCCTGCAGGGCTGCGCCCCCTGAAACGGCTTCGCAGAGCCTCCACTAGCACAGGC AAGCACGGGCTCCTGCAGGGCTGCGCCCCCTGGAACGGCTTCGCAGAGCCTCCACTAGCACAGGC T C PCID2 Ensembl:ENSG00000126226 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113184877..113184948 26863196 MeRIP-seq:(Medium) rs1161874110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6318417,Human_RBP_ID_12102441,Human_RBP_ID_18636836 RMVar_hsa_circ_23786,RMVar_hsa_circ_34806,RMVar_hsa_circ_100487,RMVar_hsa_circ_164886,RMVar_hsa_circ_332201,RMVar_hsa_circ_274678,RMVar_hsa_circ_45938,RMVar_hsa_circ_164888,RMVar_hsa_circ_164890,RMVar_hsa_circ_291388,RMVar_hsa_circ_303816,RMVar_hsa_circ_326165,RMVar_hsa_circ_30287,RMVar_hsa_circ_164889 62691 RMVar_ID_62691 Human_SNP_ID_546137376 m1A Human chr13 - 113187395 113187394 113187395 AAAAACAGTGCAGCTGCTGTGCGGAAATGGGAAGGCAGTTCCTGAAAGTGGGACGTAGAGCTACC AAAAACAGTGCAGCTGCTGTGCGGAAATGGGA_GGCAGTTCCTGAAAGTGGGACGTAGAGCTACC CT C PCID2 Ensembl:ENSG00000126226 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113187344..113187433 26863196 MeRIP-seq:(Medium) rs1292685678 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_37789,Human_RBP_ID_8388010,Human_RBP_ID_12102588,Human_RBP_ID_18636841 RMVar_hsa_circ_23786,RMVar_hsa_circ_34806,RMVar_hsa_circ_100487,RMVar_hsa_circ_164886,RMVar_hsa_circ_332201,RMVar_hsa_circ_164890,RMVar_hsa_circ_303816,RMVar_hsa_circ_326165,RMVar_hsa_circ_30287,RMVar_hsa_circ_164889 62692 RMVar_ID_62692 Human_SNP_ID_546137854 m1A Human chr13 + 113189291 113189291 113189291 CTTCTTGTGCAACCTGCAGAACTGTGAGCCAAATAAACCTCTTTTCTTACATTCCCCAGCCTCAG CTTCTTGTGCAACCTGCAGAACTGTGAGCCAATTAAACCTCTTTTCTTACATTCCCCAGCCTCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113189186..113189414 26863196 MeRIP-seq:(Medium) rs1566957768 Functional Loss SNV dbSNP153 33..33 33 - - - 62693 RMVar_ID_62693 Human_SNP_ID_546142884 m1A Human chr13 - 113208797 113208797 113208797 CCGGCAGAAAGACCCCGGGCCCCCTCAGCCCGAGCGCGTCGCCGAGCCGGTCCCCAGGTTCTCCC CCGGCAGAAAGACCCCGGGCCCCCTCAGCCCGCGCGCGTCGCCGAGCCGGTCCCCAGGTTCTCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113208780..113208961 26863196 MeRIP-seq:(Medium) rs1199149728 Functional Loss SNV dbSNP153 33..33 33 - - - 62694 RMVar_ID_62694 Human_SNP_ID_546143044 m1A Human chr13 - 113209183 113209183 113209183 GCCCCGGGGCGCGCGCCTCCTGAGGGCTCGGCACCCCCACCCCGGGCGTGAGACCACCTCGAGGG GCCCCGGGGCGCGCGCCTCCTGAGGGCTCGGCCCCCCCACCCCGGGCGTGAGACCACCTCGAGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113209133..113209283 26863196 MeRIP-seq:(Medium) rs1313026980 Functional Loss SNV dbSNP153 33..33 33 - - - 62695 RMVar_ID_62695 Human_SNP_ID_546143397 m1A Human chr13 + 113209994 113209994 113209994 CCGCCCTGCAGACAGACCTCGGCTGCCCGACAACTACACGCAGGACACGTGGCGGAAGCTGCACG CCGCCCTGCAGACAGACCTCGGCTGCCCGACAGCTACACGCAGGACACGTGGCGGAAGCTGCACG A G CUL4A Ensembl:ENSG00000139842 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:113209976..113210050 26863196 MeRIP-seq:(Medium) rs1227095844 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_38096,Human_RBP_ID_5350969,Human_RBP_ID_17833892,Human_RBP_ID_18189338,Human_RBP_ID_19062347,Human_RBP_ID_22647891,Human_RBP_ID_26807851 Human_Splice_Rec_1485460,Human_Splice_Rec_1485461,Human_Splice_Rec_1485496,Human_Splice_Rec_1485497,Human_Splice_Rec_1485532,Human_Splice_Rec_1485533,Human_Splice_Rec_1485568,Human_Splice_Rec_1485569,Human_Splice_Rec_1485604,Human_Splice_Rec_1485605,Human_Splice_Rec_1485612,Human_Splice_Rec_1485613,Human_Splice_Rec_1485648,Human_Splice_Rec_1485649,Human_Splice_Rec_1485653,Human_Splice_Rec_1485659 RMVar_hsa_circ_52904,RMVar_hsa_circ_122233,RMVar_hsa_circ_62031,RMVar_hsa_circ_164896,RMVar_hsa_circ_400,RMVar_hsa_circ_9803 62696 RMVar_ID_62696 Human_SNP_ID_546146085 m1A Human chr13 + 113218991 113218991 113218991 CTGTTCTCACAAAGTCTCCCCAATGCTCTACAAGCAACTGCGTCAGGCCTGTGAAGACCACGTCC CTGTTCTCACAAAGTCTCCCCAATGCTCTACAGGCAACTGCGTCAGGCCTGTGAAGACCACGTCC A G CUL4A Ensembl:ENSG00000139842 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113218976..113219000 26863196 MeRIP-seq:(Medium) rs1355778034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38097,Human_RBP_ID_1805196,Human_RBP_ID_2375174,Human_RBP_ID_12103374,Human_RBP_ID_18636872,Human_RBP_ID_24469006,Human_RBP_ID_26324531 Human_Splice_Rec_1485462,Human_Splice_Rec_1485498,Human_Splice_Rec_1485534,Human_Splice_Rec_1485570,Human_Splice_Rec_1485606,Human_Splice_Rec_1485614,Human_Splice_Rec_1485650,Human_Splice_Rec_1485652,Human_Splice_Rec_1485654,Human_Splice_Rec_1485660 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_122233,RMVar_hsa_circ_62031,RMVar_hsa_circ_164896,RMVar_hsa_circ_400,RMVar_hsa_circ_9803,RMVar_hsa_circ_272744,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164903,RMVar_hsa_circ_164900 62697 RMVar_ID_62697 Human_SNP_ID_546149183 m1A Human chr13 - 113229922 113229922 113229922 GACGATGAGTGCTATGTGCTCAGGAGGCCGGGAGGCTGAGCAAGCCATTCCACAGGGGACGCACA GACGATGAGTGCTATGTGCTCAGGAGGCCGGGGGGCTGAGCAAGCCATTCCACAGGGGACGCACA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:113229876..113230025 32194978 MeRIP-seq:(Medium) rs1183085891 Functional Loss SNV dbSNP153 33..33 33 - - - 62698 RMVar_ID_62698 Human_SNP_ID_546149586 m1A Human chr13 + 113231241 113231241 113231241 AAGAAGAATCCTGGTTGAGGTGTGTGTGGGCAATGCATGGTGAGGAGATACTTTGTCCATCTCTG AAGAAGAATCCTGGTTGAGGTGTGTGTGGGCAGTGCATGGTGAGGAGATACTTTGTCCATCTCTG A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113231226..113231413 26863196 MeRIP-seq:(Medium) rs376003519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19062349,Human_RBP_ID_23586009 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_62031,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164900,RMVar_hsa_circ_164904,RMVar_hsa_circ_110493 62699 RMVar_ID_62699 Human_SNP_ID_546149597 m1A Human chr13 + 113231276 113231276 113231276 CATGGTGAGGAGATACTTTGTCCATCTCTGGGATGGGGAGGAGGGCTGAGGGTGAACCTTGGCCT CATGGTGAGGAGATACTTTGTCCATCTCTGGGGTGGGGAGGAGGGCTGAGGGTGAACCTTGGCCT A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113231274..113231378 26863196 MeRIP-seq:(Medium) rs1044736233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196055,Human_RBP_ID_6259415,Human_RBP_ID_22914078,Human_RBP_ID_23586010 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_62031,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164900,RMVar_hsa_circ_164904,RMVar_hsa_circ_110493 62700 RMVar_ID_62700 Human_SNP_ID_546149875 m1A Human chr13 + 113232041 113232041 113232041 CTGCCACCACCACCACCACCATTACTGCTGCCACCACTACCCGCCCACCACCATTACTGTCACCA CTGCCACCACCACCACCACCATTACTGCTGCCGCCACTACCCGCCCACCACCATTACTGTCACCA A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113231879..113232072 26863196 MeRIP-seq:(Medium) rs1346916527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17076238 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_62031,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164900,RMVar_hsa_circ_164904,RMVar_hsa_circ_110493 62701 RMVar_ID_62701 Human_SNP_ID_546150170 m1A Human chr13 + 113232335 113232335 113232335 CCACTATTACTGCTGCTGCCACCACCAGTATTACTGTCACCGCCACCACCGCTATTACTACTGCC CCACTATTACTGCTGCTGCCACCACCAGTATTGCTGTCACCGCCACCACCGCTATTACTACTGCC A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113232284..113232420 26863196 MeRIP-seq:(Medium) rs954706932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196064,Human_RBP_ID_5127449,Human_RBP_ID_17076054,Human_RBP_ID_26807853 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_62031,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164900,RMVar_hsa_circ_164904,RMVar_hsa_circ_110493 62702 RMVar_ID_62702 Human_SNP_ID_546150338 m1A Human chr13 + 113232745 113232745 113232745 CTCCCAGGGCTTGGAGAAGGGAAGCTGCTGGGACGTGCTCAGCAGAGGACACTGGGAAGAGAGTG CTCCCAGGGCTTGGAGAAGGGAAGCTGCTGGGGCGTGCTCAGCAGAGGACACTGGGAAGAGAGTG A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113232728..113232899 26863196 MeRIP-seq:(Medium) rs145672885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196066,Human_RBP_ID_22914081 RMVar_hsa_circ_1028,RMVar_hsa_circ_52904,RMVar_hsa_circ_62031,RMVar_hsa_circ_339053,RMVar_hsa_circ_346785,RMVar_hsa_circ_330934,RMVar_hsa_circ_14287,RMVar_hsa_circ_34635,RMVar_hsa_circ_3329,RMVar_hsa_circ_164899,RMVar_hsa_circ_164901,RMVar_hsa_circ_164902,RMVar_hsa_circ_164900,RMVar_hsa_circ_164904,RMVar_hsa_circ_110493 62703 RMVar_ID_62703 Human_SNP_ID_546150561 m1A Human chr13 - 113233330 113233330 113233330 TCTTCCGCACAGGCAGCACTCACCTGCAGGTCAGACAGCATGCCCAGGAGGCTCCGCAACAGGCT TCTTCCGCACAGGCAGCACTCACCTGCAGGTCGGACAGCATGCCCAGGAGGCTCCGCAACAGGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:113233228..113233350 32194978 MeRIP-seq:(Medium) rs966535875 Functional Loss SNV dbSNP153 33..33 33 - - - 62704 RMVar_ID_62704 Human_SNP_ID_546150562 m1A Human chr13 - 113233330 113233330 113233330 TCTTCCGCACAGGCAGCACTCACCTGCAGGTCAGACAGCATGCCCAGGAGGCTCCGCAACAGGCT TCTTCCGCACAGGCAGCACTCACCTGCAGGTCCGACAGCATGCCCAGGAGGCTCCGCAACAGGCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:113233228..113233350 32194978 MeRIP-seq:(Medium) rs966535875 Functional Loss SNV dbSNP153 33..33 33 - - - 62705 RMVar_ID_62705 Human_SNP_ID_546155479 m1A Human chr13 + 113251201 113251201 113251201 AGATGCTGGTAGAGCTAAGAGGGTGTCAGAGAAGACCTCTCTGAGGAGGCGGTTCTGGAAATGAG AGATGCTGGTAGAGCTAAGAGGGTGTCAGAGACGACCTCTCTGAGGAGGCGGTTCTGGAAATGAG A C CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113251197..113251417 26863196 MeRIP-seq:(Medium) rs375394984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14287,RMVar_hsa_circ_3329,RMVar_hsa_circ_7455,RMVar_hsa_circ_63154,RMVar_hsa_circ_356424,RMVar_hsa_circ_51009,RMVar_hsa_circ_29416,RMVar_hsa_circ_36382,RMVar_hsa_circ_357153,RMVar_hsa_circ_364984,RMVar_hsa_circ_24974,RMVar_hsa_circ_28182,RMVar_hsa_circ_73822 62706 RMVar_ID_62706 Human_SNP_ID_546155485 m1A Human chr13 + 113251228 113251228 113251228 AGAGAAGACCTCTCTGAGGAGGCGGTTCTGGAAATGAGTAGGTTTCATGAGGGAGATGGGATATG AGAGAAGACCTCTCTGAGGAGGCGGTTCTGGATATGAGTAGGTTTCATGAGGGAGATGGGATATG A T CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113251226..113251430 26863196 MeRIP-seq:(Medium) rs993936478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14287,RMVar_hsa_circ_3329,RMVar_hsa_circ_7455,RMVar_hsa_circ_63154,RMVar_hsa_circ_356424,RMVar_hsa_circ_51009,RMVar_hsa_circ_29416,RMVar_hsa_circ_36382,RMVar_hsa_circ_357153,RMVar_hsa_circ_364984,RMVar_hsa_circ_24974,RMVar_hsa_circ_28182,RMVar_hsa_circ_73822 62707 RMVar_ID_62707 Human_SNP_ID_546170838 m1A Human chr13 + 113306517 113306517 113306517 GCCTCATGCATTGTGCGTCAGCAGCAATGTTTATGGTGAAAAATGGCAACGGGACCGCGTGCATA GCCTCATGCATTGTGCGTCAGCAGCAATGTTTGTGGTGAAAAATGGCAACGGGACCGCGTGCATA A G LAMP1 Ensembl:ENSG00000185896 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113306476..113306550 26863196 MeRIP-seq:(Medium) rs748693352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1805289,Human_RBP_ID_4276529,Human_RBP_ID_8388256,Human_RBP_ID_17475577,Human_RBP_ID_19829811,Human_RBP_ID_22438365,Human_RBP_ID_22737312 Human_Splice_Rec_1485688,Human_Splice_Rec_1485689,Human_Splice_Rec_1485703 RMVar_hsa_circ_77204,RMVar_hsa_circ_87658,RMVar_hsa_circ_164911,RMVar_hsa_circ_164910,RMVar_hsa_circ_164912,RMVar_hsa_circ_279299,RMVar_hsa_circ_300709,RMVar_hsa_circ_371638,RMVar_hsa_circ_83132,RMVar_hsa_circ_164914,RMVar_hsa_circ_164916,RMVar_hsa_circ_164918,RMVar_hsa_circ_75946,RMVar_hsa_circ_164917,RMVar_hsa_circ_164915,RMVar_hsa_circ_164913 62708 RMVar_ID_62708 Human_SNP_ID_546171849 m1A Human chr13 + 113309756 113309756 113309756 AGTCTCGTGATTGCTTTTGGAAGAGGACATACACTCACTCTCAATTTCACGAGAAATGCAACACG AGTCTCGTGATTGCTTTTGGAAGAGGACATACGCTCACTCTCAATTTCACGAGAAATGCAACACG A G LAMP1 Ensembl:ENSG00000185896 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113309705..113309802 26863196 MeRIP-seq:(Medium) rs1226870090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38190,Human_RBP_ID_995627,Human_RBP_ID_1271537,Human_RBP_ID_8072529,Human_RBP_ID_9028568,Human_RBP_ID_9280255,Human_RBP_ID_17244006,Human_RBP_ID_17359007,Human_RBP_ID_17475578,Human_RBP_ID_17685962,Human_RBP_ID_17833942,Human_RBP_ID_18527677,Human_RBP_ID_22421244,Human_RBP_ID_22757485,Human_RBP_ID_26807588 Human_miRNA_ID_2382958,Human_miRNA_ID_2382959 RMVar_hsa_circ_108445,RMVar_hsa_circ_77204,RMVar_hsa_circ_87658,RMVar_hsa_circ_164910,RMVar_hsa_circ_164912,RMVar_hsa_circ_279299,RMVar_hsa_circ_300709,RMVar_hsa_circ_371638,RMVar_hsa_circ_83132,RMVar_hsa_circ_164914,RMVar_hsa_circ_164916,RMVar_hsa_circ_164918,RMVar_hsa_circ_75946,RMVar_hsa_circ_164917,RMVar_hsa_circ_164915,RMVar_hsa_circ_164913,RMVar_hsa_circ_294012,RMVar_hsa_circ_164919,RMVar_hsa_circ_57857,RMVar_hsa_circ_108292,RMVar_hsa_circ_164920,RMVar_hsa_circ_164921 62709 RMVar_ID_62709 Human_SNP_ID_546172193 m1A Human chr13 + 113310810 113310810 113310810 GCACCCAGGTCCACATGAACAACGTGACCGTAACGCTCCATGATGCCACCATCCAGGCGTACCTT GCACCCAGGTCCACATGAACAACGTGACCGTAGCGCTCCATGATGCCACCATCCAGGCGTACCTT A G LAMP1 Ensembl:ENSG00000185896 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113310762..113310920 26863196 MeRIP-seq:(Medium) rs1186662794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756139,Human_RBP_ID_1359215,Human_RBP_ID_12104590,Human_RBP_ID_22757488 Human_Splice_Rec_1485693,Human_Splice_Rec_1485707 Human_miRNA_ID_687706,Human_miRNA_ID_1957272,Human_miRNA_ID_2276870 RMVar_hsa_circ_108445,RMVar_hsa_circ_77204,RMVar_hsa_circ_87658,RMVar_hsa_circ_164910,RMVar_hsa_circ_279299,RMVar_hsa_circ_371638,RMVar_hsa_circ_83132,RMVar_hsa_circ_164914,RMVar_hsa_circ_164916,RMVar_hsa_circ_75946,RMVar_hsa_circ_164917,RMVar_hsa_circ_164915,RMVar_hsa_circ_164913,RMVar_hsa_circ_57857,RMVar_hsa_circ_108292,RMVar_hsa_circ_164920,RMVar_hsa_circ_164921,RMVar_hsa_circ_35448,RMVar_hsa_circ_90822,RMVar_hsa_circ_164922 62710 RMVar_ID_62710 Human_SNP_ID_546172962 m1A Human chr13 + 113313606 113313606 113313606 CGGTGTGCCTGGGGCGTGGCCTCCTGGAGGGAACCAGTGTGGAGATGTCGGTGTGCCTGGGGTGT CGGTGTGCCTGGGGCGTGGCCTCCTGGAGGGAGCCAGTGTGGAGATGTCGGTGTGCCTGGGGTGT A G LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113313601..113313908 26863196 MeRIP-seq:(Medium) rs1384456545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17114888 RMVar_hsa_circ_108445,RMVar_hsa_circ_77204,RMVar_hsa_circ_87658,RMVar_hsa_circ_164910,RMVar_hsa_circ_371638,RMVar_hsa_circ_83132,RMVar_hsa_circ_164914,RMVar_hsa_circ_164916,RMVar_hsa_circ_75946,RMVar_hsa_circ_164915,RMVar_hsa_circ_164913,RMVar_hsa_circ_108292,RMVar_hsa_circ_164920,RMVar_hsa_circ_164921,RMVar_hsa_circ_35448 62711 RMVar_ID_62711 Human_SNP_ID_546174898 m1A Human chr13 - 113319515 113319506 113319515 GGCACGGGTGAGGGCGAGGGGCTGGGTGGCGCAGGGGGCGCTGTGGTTGGGGAAGGCCTGTCTTG GGCACGGGTGAGGGCGAGGGGCTGGGTGGCGC_________TGTGGTTGGGGAAGGCCTGTCTTG AGCGCCCCCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr13:113319445..113319603;chr13:113319431..113319592;chr13:113319501..113319525 26863196 MeRIP-seq:(Medium) rs1346486401 Functional Loss DEL dbSNP153 33..41 33 - - - 62712 RMVar_ID_62712 Human_SNP_ID_546175154 m1A Human chr13 - 113320298 113320298 113320298 CAAGCAAGTCACCACCCTAGCTCAGGTCCTCCACACTCTCGAAAAGACAAACAGTCCTGAAACCG CAAGCAAGTCACCACCCTAGCTCAGGTCCTCCCCACTCTCGAAAAGACAAACAGTCCTGAAACCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113320295..113320425 26863196 MeRIP-seq:(Medium) rs537221592 Functional Loss SNV dbSNP153 33..33 33 - - - 62713 RMVar_ID_62713 Human_SNP_ID_546175856 m1A Human chr13 - 113322381 113322381 113322381 TCTGGTAGCCTGCGTGACTCCTCTTCCTGCCGACGAGGTAGGCGATGAGGACGATGAGGACCAGC TCTGGTAGCCTGCGTGACTCCTCTTCCTGCCGGCGAGGTAGGCGATGAGGACGATGAGGACCAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113322331..113322700 26863196 MeRIP-seq:(Medium) rs768578956 Functional Loss SNV dbSNP153 33..33 33 - - - 62714 RMVar_ID_62714 Human_SNP_ID_546176089 m1A Human chr13 + 113322869 113322869 113322869 TCTCTCCGAGGGGTGGAATGCCGCTGTCTCTGAGGGGTGGGGGTGCCGCTCTAAATTGGCTCCAT TCTCTCCGAGGGGTGGAATGCCGCTGTCTCTGGGGGGTGGGGGTGCCGCTCTAAATTGGCTCCAT A G LAMP1 Ensembl:ENSG00000185896 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113322700..113323109 26863196 MeRIP-seq:(Medium) rs1197587486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_432473,Human_RBP_ID_1169172,Human_RBP_ID_6259628,Human_RBP_ID_8180271,Human_RBP_ID_9028574,Human_RBP_ID_9352894,Human_RBP_ID_17685965,Human_RBP_ID_23586101,Human_RBP_ID_26426604 RMVar_hsa_circ_108445,RMVar_hsa_circ_87658,RMVar_hsa_circ_164910,RMVar_hsa_circ_75946,RMVar_hsa_circ_164913,RMVar_hsa_circ_79636,RMVar_hsa_circ_164921,RMVar_hsa_circ_127196,RMVar_hsa_circ_121883,RMVar_hsa_circ_164924,RMVar_hsa_circ_164925,RMVar_hsa_circ_101682,RMVar_hsa_circ_91340,RMVar_hsa_circ_164926,RMVar_hsa_circ_164927,RMVar_hsa_circ_164928 62715 RMVar_ID_62715 Human_SNP_ID_546176101 m1A Human chr13 - 113322922 113322922 113322922 GAGTGCAGTAAAGAATGAAGAAACCAAACACCAGAACCCTAAACTCAAATGATATGGAGCCAATT GAGTGCAGTAAAGAATGAAGAAACCAAACACCGGAACCCTAAACTCAAATGATATGGAGCCAATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113322872..113322981 26863196 MeRIP-seq:(Medium) rs1235265147 Functional Loss SNV dbSNP153 33..33 33 - - - 62716 RMVar_ID_62716 Human_SNP_ID_546176279 m1A Human chr13 + 113323468 113323468 113323468 CCTTGTCCTTCTGTCAGCTAAAATGGGAGCTCATGAGAGAAGGACGTCAGGGAAACGGGGTTGAG CCTTGTCCTTCTGTCAGCTAAAATGGGAGCTCCTGAGAGAAGGACGTCAGGGAAACGGGGTTGAG A C LAMP1 Ensembl:ENSG00000185896 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113323418..113323600 26863196 MeRIP-seq:(Medium) rs369008429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_432493,Human_RBP_ID_6259648,Human_RBP_ID_9352896,Human_RBP_ID_12104746 62717 RMVar_ID_62717 Human_SNP_ID_546188095 m1A Human chr13 + 113355424 113355406 113355424 TCTGGTCCATCTGCGCCTGGGCCCCACTCAGCACCATCCAGACGCGGGCACGGTGCTCCAGCGGG TCTGGTCCATCTGCG__________________CCATCCAGACGCGGGCACGGTGCTCCAGCGGG GCCTGGGCCCCACTCAGCA G GRTP1-AS1 Ensembl:ENSG00000225083 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113355392..113355536 26863196 MeRIP-seq:(Medium) rs1566440722 Functional Loss DEL dbSNP153 16..33 33 - - - 62718 RMVar_ID_62718 Human_SNP_ID_546190478 m1A Human chr13 + 113364070 113364070 113364070 TCGGCGGGCTGCATGCGGGGAGGGAGGCGCGCACCGAGCGAGGCCAGCGGGTCCCAAGTTCGCCT TCGGCGGGCTGCATGCGGGGAGGGAGGCGCGCGCCGAGCGAGGCCAGCGGGTCCCAAGTTCGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113363983..113364108 26863196 MeRIP-seq:(Medium) rs764714862 Functional Loss SNV dbSNP153 33..33 33 - - - 62719 RMVar_ID_62719 Human_SNP_ID_546205359 m1A Human chr13 + 113412783 113412749 113412784 TCGGTTCACCCACCGCCAACAGCGCCCCGCAGAACTCGGTTCACCCACCGCCAACAGCACCCCGC __________________________________CTCGGTTCACCCACCGCCAACAGCACCCCGC GCTCGGTTCACCCACCGCCAACAGCGCCCCGCAGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113412748..113412862 26863196 MeRIP-seq:(Medium) rs1566467618 Functional Loss DEL dbSNP153 1..34 33 - - - 62720 RMVar_ID_62720 Human_SNP_ID_546205378 m1A Human chr13 + 113412783 113412775 113412784 TCGGTTCACCCACCGCCAACAGCGCCCCGCAGAACTCGGTTCACCCACCGCCAACAGCACCCCGC TCGGTTCACCCACCGCCAACAGCGC_________CTCGGTTCACCCACCGCCAACAGCACCCCGC CCCCGCAGAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113412748..113412862 26863196 MeRIP-seq:(Medium) rs1243562598 Functional Loss DEL dbSNP153 26..34 33 - - - 62721 RMVar_ID_62721 Human_SNP_ID_546212333 m1A Human chr13 - 113433807 113433807 113433807 CATGTGCATCGGCCTGCGGTACTGGAAGCCTGAGCGGCTGGAGACCCTCATCGAGGTCAGCGTGG CATGTGCATCGGCCTGCGGTACTGGAAGCCTGGGCGGCTGGAGACCCTCATCGAGGTCAGCGTGG T C ADPRHL1 Ensembl:ENSG00000153531 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113433706..113433822 26863196 MeRIP-seq:(Medium) rs557040870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1485772,Human_Splice_Rec_1485773,Human_Splice_Rec_1485786,Human_Splice_Rec_1485787,Human_Splice_Rec_1485798,Human_Splice_Rec_1485799,Human_Splice_Rec_1485810,Human_Splice_Rec_1485811 RMVar_hsa_circ_13825,RMVar_hsa_circ_77121,RMVar_hsa_circ_120447,RMVar_hsa_circ_164935,RMVar_hsa_circ_164934 62722 RMVar_ID_62722 Human_SNP_ID_546217689 m1A Human chr13 - 113449432 113449432 113449432 GTGTGTCTCTCTGAACGGGGCTCACTCCTTCCAGGTGTGTCTCTCTGAACAGGGCTGCCTCCTTC GTGTGTCTCTCTGAACGGGGCTCACTCCTTCCGGGTGTGTCTCTCTGAACAGGGCTGCCTCCTTC T C ADPRHL1 Ensembl:ENSG00000153531 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113449407..113449519 26863196 MeRIP-seq:(Medium) rs56332458 Functional Loss SNV dbSNP153 33..33 33 - - - 62723 RMVar_ID_62723 Human_SNP_ID_546224981 m1A Human chr13 - 113472950 113472949 113472950 ACAGAAGGACAGAGGTACGGGAGCAGAGGCGCAGGGGGACACGGGAGAGAGACGGGGCTGGTGAG ACAGAAGGACAGAGGTACGGGAGCAGAGGCGC_GGGGGACACGGGAGAGAGACGGGGCTGGTGAG CT C DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113472926..113473070 26863196 MeRIP-seq:(Medium) rs1169792046 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3439922,Human_RBP_ID_5235901,Human_RBP_ID_8180275,Human_RBP_ID_9417277 RMVar_hsa_circ_305861,RMVar_hsa_circ_265899,RMVar_hsa_circ_66111 62724 RMVar_ID_62724 Human_SNP_ID_546225052 m1A Human chr13 - 113473157 113473155 113473157 ACGGGACAGAGGGATAGAGAGACGGGGGACAGAGGGACAGAGGCACAGGAGACAGAGGGATAGAG ACGGGACAGAGGGATAGAGAGACGGGGGACAG__GGACAGAGGCACAGGAGACAGAGGGATAGAG CCT C DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:113473010..113473161 26863196 MeRIP-seq:(Medium) rs1214904806 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_305861,RMVar_hsa_circ_265899,RMVar_hsa_circ_66111 62725 RMVar_ID_62725 Human_SNP_ID_546225068 m1A Human chr13 + 113473212 113473212 113473212 TCTGTCCCGTGTCTCTGCCCTTCTGTGCCTGCATTCCTTGTCCTTCTGCCCCGTGCCTCTGCCTC TCTGTCCCGTGTCTCTGCCCTTCTGTGCCTGCGTTCCTTGTCCTTCTGCCCCGTGCCTCTGCCTC A G DCUN1D2-AS Ensembl:ENSG00000233613 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113472907..113473317 26863196 MeRIP-seq:(Medium) rs976058490 Functional Loss SNV dbSNP153 33..33 33 - - - 62726 RMVar_ID_62726 Human_SNP_ID_546229295 m1A Human chr13 - 113489503 113489503 113489503 GAGAAACCAGGACACTAGAATGTGTCGAAACCAAGAGGATGGAGTTTAAAGGAGGAGGGAGCCAT GAGAAACCAGGACACTAGAATGTGTCGAAACCGAGAGGATGGAGTTTAAAGGAGGAGGGAGCCAT T C DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113489452..113489762 26863196 MeRIP-seq:(Medium) rs1379225302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2375784,Human_RBP_ID_12105679 62727 RMVar_ID_62727 Human_SNP_ID_546229300 m1A Human chr13 - 113489527 113489527 113489527 AGGAGACTGAGAGGGGGCTGGTAGGAGAAACCAGGACACTAGAATGTGTCGAAACCAAGAGGATG AGGAGACTGAGAGGGGGCTGGTAGGAGAAACCGGGACACTAGAATGTGTCGAAACCAAGAGGATG T C DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113489478..113489756 26863196 MeRIP-seq:(Medium) rs968350752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6259957,Human_RBP_ID_12105680 62728 RMVar_ID_62728 Human_SNP_ID_546229600 m1A Human chr13 - 113490528 113490528 113490528 GCGCGGGGCGTTCCGCGTGGATCCGAGGGAGGAACGCGCCGCGGGCCCGCGAGCCGGAGCGGTGG GCGCGGGGCGTTCCGCGTGGATCCGAGGGAGGGACGCGCCGCGGGCCCGCGAGCCGGAGCGGTGG T C DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113490442..113490692 26863196 MeRIP-seq:(Medium) rs1248848908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3438879,Human_RBP_ID_9352881,Human_RBP_ID_9417278,Human_RBP_ID_18480162,Human_RBP_ID_22919909 Human_Splice_Rec_1485851,Human_Splice_Rec_1485881 62729 RMVar_ID_62729 Human_SNP_ID_546229942 m1A Human chr13 + 113491137 113491137 113491137 TCCCTGGTCCCGCCTGGGAAGGGATGCAAGGAAGCCCTCCGGCGCTGCGCTCCGAGGCGGGAGAC TCCCTGGTCCCGCCTGGGAAGGGATGCAAGGACGCCCTCCGGCGCTGCGCTCCGAGGCGGGAGAC A C TMCO3 Ensembl:ENSG00000150403 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:113491051..113491183 26863196 MeRIP-seq:(Medium) rs1453877828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276532,Human_RBP_ID_18469376 RMVar_hsa_circ_78543,RMVar_hsa_circ_102850,RMVar_hsa_circ_164937,RMVar_hsa_circ_164938 62730 RMVar_ID_62730 Human_SNP_ID_546235101 m1A Human chr13 - 113509117 113509117 113509117 GCACCTCCAGGGGGGACCCACCCACCAAGCCCACCAGCCCCAACATACACAGGCAGTGTCAGGGG GCACCTCCAGGGGGGACCCACCCACCAAGCCCGCCAGCCCCAACATACACAGGCAGTGTCAGGGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113509060..113509190 26863196 MeRIP-seq:(Medium) rs113333662 Functional Loss SNV dbSNP153 33..33 33 - - - 62731 RMVar_ID_62731 Human_SNP_ID_546235102 m1A Human chr13 - 113509117 113509117 113509117 GCACCTCCAGGGGGGACCCACCCACCAAGCCCACCAGCCCCAACATACACAGGCAGTGTCAGGGG GCACCTCCAGGGGGGACCCACCCACCAAGCCCCCCAGCCCCAACATACACAGGCAGTGTCAGGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113509060..113509190 26863196 MeRIP-seq:(Medium) rs113333662 Functional Loss SNV dbSNP153 33..33 33 - - - 62732 RMVar_ID_62732 Human_SNP_ID_546236072 m1A Human chr13 + 113511943 113511939 113511943 GGTGTGCAGTATATATACACTCGGAGTCACGGAGGCCGGGACTGGAGAGGCAGAGGGCCGGAGTG GGTGTGCAGTATATATACACTCGGAGTCGCAGGGGCCGGGACTGGAGAGGCAGAGGGCCGGAGTG ACGGA GCAGG AL442125.2,TMCO3 Ensembl:ENSG00000276916,Ensembl:ENSG00000150403 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113511737..113511979 26863196 MeRIP-seq:(Medium) rs796866993 Functional Loss MNV dbSNP153 29..33 33 - - - Human_Splice_Rec_1485979 Human_miRNA_ID_3177290 RMVar_hsa_circ_102850,RMVar_hsa_circ_271284,RMVar_hsa_circ_164938,RMVar_hsa_circ_323964,RMVar_hsa_circ_274859,RMVar_hsa_circ_104733,RMVar_hsa_circ_85943,RMVar_hsa_circ_164940,RMVar_hsa_circ_164942,RMVar_hsa_circ_164943,RMVar_hsa_circ_164941,RMVar_hsa_circ_113394,RMVar_hsa_circ_164949,RMVar_hsa_circ_164939,RMVar_hsa_circ_286804,RMVar_hsa_circ_164950,RMVar_hsa_circ_40253,RMVar_hsa_circ_95642,RMVar_hsa_circ_114264,RMVar_hsa_circ_164951,RMVar_hsa_circ_164955,RMVar_hsa_circ_275248,RMVar_hsa_circ_292965,RMVar_hsa_circ_119165,RMVar_hsa_circ_164956,RMVar_hsa_circ_164957,RMVar_hsa_circ_164958,RMVar_hsa_circ_270995,RMVar_hsa_circ_272653,RMVar_hsa_circ_275146,RMVar_hsa_circ_126748,RMVar_hsa_circ_164959,RMVar_hsa_circ_164961,RMVar_hsa_circ_164962,RMVar_hsa_circ_164963,RMVar_hsa_circ_164960 62733 RMVar_ID_62733 Human_SNP_ID_546236077 m1A Human chr13 + 113511943 113511943 113511943 GGTGTGCAGTATATATACACTCGGAGTCACGGAGGCCGGGACTGGAGAGGCAGAGGGCCGGAGTG GGTGTGCAGTATATATACACTCGGAGTCACGGGGGCCGGGACTGGAGAGGCAGAGGGCCGGAGTG A G AL442125.2,TMCO3 Ensembl:ENSG00000276916,Ensembl:ENSG00000150403 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113511737..113511979 26863196 MeRIP-seq:(Medium) rs369667356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1485979 Human_miRNA_ID_3177290 RMVar_hsa_circ_102850,RMVar_hsa_circ_271284,RMVar_hsa_circ_164938,RMVar_hsa_circ_323964,RMVar_hsa_circ_274859,RMVar_hsa_circ_104733,RMVar_hsa_circ_85943,RMVar_hsa_circ_164940,RMVar_hsa_circ_164942,RMVar_hsa_circ_164943,RMVar_hsa_circ_164941,RMVar_hsa_circ_113394,RMVar_hsa_circ_164949,RMVar_hsa_circ_164939,RMVar_hsa_circ_286804,RMVar_hsa_circ_164950,RMVar_hsa_circ_40253,RMVar_hsa_circ_95642,RMVar_hsa_circ_114264,RMVar_hsa_circ_164951,RMVar_hsa_circ_164955,RMVar_hsa_circ_275248,RMVar_hsa_circ_292965,RMVar_hsa_circ_119165,RMVar_hsa_circ_164956,RMVar_hsa_circ_164957,RMVar_hsa_circ_164958,RMVar_hsa_circ_270995,RMVar_hsa_circ_272653,RMVar_hsa_circ_275146,RMVar_hsa_circ_126748,RMVar_hsa_circ_164959,RMVar_hsa_circ_164961,RMVar_hsa_circ_164962,RMVar_hsa_circ_164963,RMVar_hsa_circ_164960 62734 RMVar_ID_62734 Human_SNP_ID_546236123 m1A Human chr13 - 113512042 113512042 113512042 ATATATATACTGACCCTCTCCATCTACACTCCAACCCTCTCCCTCTCCAGTCCCGGCCCCCGCGA ATATATATACTGACCCTCTCCATCTACACTCCGACCCTCTCCCTCTCCAGTCCCGGCCCCCGCGA T C lnc-DCUN1D2-1 RNACentral:URS00008BDB55 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113512035..113512185 26863196 MeRIP-seq:(Medium) rs1220734850 Functional Loss SNV dbSNP153 33..33 33 - - - 62735 RMVar_ID_62735 Human_SNP_ID_546236124 m1A Human chr13 - 113512042 113512042 113512042 ATATATATACTGACCCTCTCCATCTACACTCCAACCCTCTCCCTCTCCAGTCCCGGCCCCCGCGA ATATATATACTGACCCTCTCCATCTACACTCCCACCCTCTCCCTCTCCAGTCCCGGCCCCCGCGA T G lnc-DCUN1D2-1 RNACentral:URS00008BDB55 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113512035..113512185 26863196 MeRIP-seq:(Medium) rs1220734850 Functional Loss SNV dbSNP153 33..33 33 - - - 62736 RMVar_ID_62736 Human_SNP_ID_546236220 m1A Human chr13 + 113512266 113512266 113512266 CGGGGGCCGGGACTGGAGAGGGAGAGGGTTGGAGTGTAGATGGAGAGGGTCAGTATATATATACA CGGGGGCCGGGACTGGAGAGGGAGAGGGTTGGGGTGTAGATGGAGAGGGTCAGTATATATATACA A G AL442125.2,TMCO3 Ensembl:ENSG00000276916,Ensembl:ENSG00000150403 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113512261..113512962 26863196 MeRIP-seq:(Medium) rs2490980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102850,RMVar_hsa_circ_271284,RMVar_hsa_circ_164938,RMVar_hsa_circ_323964,RMVar_hsa_circ_274859,RMVar_hsa_circ_104733,RMVar_hsa_circ_85943,RMVar_hsa_circ_164940,RMVar_hsa_circ_164942,RMVar_hsa_circ_164943,RMVar_hsa_circ_164941,RMVar_hsa_circ_113394,RMVar_hsa_circ_164949,RMVar_hsa_circ_164939,RMVar_hsa_circ_286804,RMVar_hsa_circ_164950,RMVar_hsa_circ_40253,RMVar_hsa_circ_95642,RMVar_hsa_circ_114264,RMVar_hsa_circ_164951,RMVar_hsa_circ_164955,RMVar_hsa_circ_275248,RMVar_hsa_circ_292965,RMVar_hsa_circ_119165,RMVar_hsa_circ_164956,RMVar_hsa_circ_164957,RMVar_hsa_circ_164958,RMVar_hsa_circ_270995,RMVar_hsa_circ_272653,RMVar_hsa_circ_275146,RMVar_hsa_circ_126748,RMVar_hsa_circ_164959,RMVar_hsa_circ_164961,RMVar_hsa_circ_164962,RMVar_hsa_circ_164963,RMVar_hsa_circ_164960 62737 RMVar_ID_62737 Human_SNP_ID_546236221 m1A Human chr13 + 113512266 113512266 113512266 CGGGGGCCGGGACTGGAGAGGGAGAGGGTTGGAGTGTAGATGGAGAGGGTCAGTATATATATACA CGGGGGCCGGGACTGGAGAGGGAGAGGGTTGGTGTGTAGATGGAGAGGGTCAGTATATATATACA A T AL442125.2,TMCO3 Ensembl:ENSG00000276916,Ensembl:ENSG00000150403 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113512261..113512962 26863196 MeRIP-seq:(Medium) rs2490980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102850,RMVar_hsa_circ_271284,RMVar_hsa_circ_164938,RMVar_hsa_circ_323964,RMVar_hsa_circ_274859,RMVar_hsa_circ_104733,RMVar_hsa_circ_85943,RMVar_hsa_circ_164940,RMVar_hsa_circ_164942,RMVar_hsa_circ_164943,RMVar_hsa_circ_164941,RMVar_hsa_circ_113394,RMVar_hsa_circ_164949,RMVar_hsa_circ_164939,RMVar_hsa_circ_286804,RMVar_hsa_circ_164950,RMVar_hsa_circ_40253,RMVar_hsa_circ_95642,RMVar_hsa_circ_114264,RMVar_hsa_circ_164951,RMVar_hsa_circ_164955,RMVar_hsa_circ_275248,RMVar_hsa_circ_292965,RMVar_hsa_circ_119165,RMVar_hsa_circ_164956,RMVar_hsa_circ_164957,RMVar_hsa_circ_164958,RMVar_hsa_circ_270995,RMVar_hsa_circ_272653,RMVar_hsa_circ_275146,RMVar_hsa_circ_126748,RMVar_hsa_circ_164959,RMVar_hsa_circ_164961,RMVar_hsa_circ_164962,RMVar_hsa_circ_164963,RMVar_hsa_circ_164960 62738 RMVar_ID_62738 Human_SNP_ID_546246256 m1A Human chr13 + 113546214 113546214 113546214 ACCAGTGTGGCCAAAGGCAGCCTGGACCGGGCATTGCAGCAGGGCAGAGGCACAGACATCCTGAG ACCAGTGTGGCCAAAGGCAGCCTGGACCGGGCGTTGCAGCAGGGCAGAGGCACAGACATCCTGAG A G TMCO3 Ensembl:ENSG00000150403 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113546203..113546557 26863196 MeRIP-seq:(Medium) rs1194172994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439967,Human_RBP_ID_8388450 RMVar_hsa_circ_104733,RMVar_hsa_circ_85943,RMVar_hsa_circ_164940,RMVar_hsa_circ_164939,RMVar_hsa_circ_95642,RMVar_hsa_circ_126748,RMVar_hsa_circ_164964,RMVar_hsa_circ_164962,RMVar_hsa_circ_164963,RMVar_hsa_circ_87770,RMVar_hsa_circ_108432,RMVar_hsa_circ_117897,RMVar_hsa_circ_164969,RMVar_hsa_circ_164970,RMVar_hsa_circ_2657 62739 RMVar_ID_62739 Human_SNP_ID_546256363 m1A Human chr13 - 113583535 113583535 113583535 ACTAGTGTGTGCAGGAGTGTGTGTGCACTTGGAAGAGCGGGGCCGGGTGTGTGCTTGAGTGTGTG ACTAGTGTGTGCAGGAGTGTGTGTGCACTTGGGAGAGCGGGGCCGGGTGTGTGCTTGAGTGTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113583385..113583610 26863196 MeRIP-seq:(Medium) rs1239117287 Functional Loss SNV dbSNP153 33..33 33 - - - 62740 RMVar_ID_62740 Human_SNP_ID_546256672 m1A Human chr13 - 113584362 113584362 113584362 GTGGCCGGCTGTGTGCAAGAGTGTGTGTGCACATGGGGGAGCGGGGCCGGCTATGTGCACGAGTG GTGGCCGGCTGTGTGCAAGAGTGTGTGTGCACGTGGGGGAGCGGGGCCGGCTATGTGCACGAGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113584245..113584482 26863196 MeRIP-seq:(Medium) rs1488571891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23586503 62741 RMVar_ID_62741 Human_SNP_ID_546256870 m1A Human chr13 + 113584840 113584828 113584840 CCCGCGCCTCTCCGCGCCGCCCCGCGCTCCGCACCGCGCCCTCTCCGCGTCCCCGCCCGCGCGGC CCCGCGCCTCTCCGCGCCGCC____________CCGCGCCCTCTCCGCGTCCCCGCCCGCGCGGC CCCGCGCTCCGCA C TFDP1 Ensembl:ENSG00000198176 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr13:113584741..113584875;chr13:113584743..113584865 26863410 MeRIP-seq:(Medium) rs1437600343 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_432590,Human_RBP_ID_4276538,Human_RBP_ID_9323557,Human_RBP_ID_18637079,Human_RBP_ID_22532555 Human_Splice_Rec_1485981,Human_Splice_Rec_1485993,Human_Splice_Rec_1485997,Human_Splice_Rec_1486009 RMVar_hsa_circ_164972,RMVar_hsa_circ_125311 62742 RMVar_ID_62742 Human_SNP_ID_546256875 m1A Human chr13 + 113584840 113584840 113584840 CCCGCGCCTCTCCGCGCCGCCCCGCGCTCCGCACCGCGCCCTCTCCGCGTCCCCGCCCGCGCGGC CCCGCGCCTCTCCGCGCCGCCCCGCGCTCCGCGCCGCGCCCTCTCCGCGTCCCCGCCCGCGCGGC A G TFDP1 Ensembl:ENSG00000198176 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr13:113584741..113584875;chr13:113584743..113584865 26863410 MeRIP-seq:(Medium) rs994031244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_432590,Human_RBP_ID_4276538,Human_RBP_ID_9323557,Human_RBP_ID_18637079,Human_RBP_ID_22532555 Human_Splice_Rec_1485981,Human_Splice_Rec_1485993,Human_Splice_Rec_1485997,Human_Splice_Rec_1486009 RMVar_hsa_circ_164972,RMVar_hsa_circ_125311 62743 RMVar_ID_62743 Human_SNP_ID_546256879 m1A Human chr13 - 113584857 113584846 113584857 CCTGGCTGCCCGGTCCGGCCGCGCGGGCGGGGACGCGGAGAGGGCGCGGTGCGGAGCGCGGGGCG CCTGGCTGCCCGGTCCGGCCGCGCGGGCGGGG___________GCGCGGTGCGGAGCGCGGGGCG CCCTCTCCGCGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr13:113584701..113585417;chr13:113584772..113585040 26863196 MeRIP-seq:(Medium) rs1440594946 Functional Loss DEL dbSNP153 33..43 33 - - - 62744 RMVar_ID_62744 Human_SNP_ID_546257064 m1A Human chr13 + 113585301 113585301 113585301 CCTCGTGCGGAGGCGGCCCGAGGCCTAGTGACAGGCGCGCGGCGCGGACCCCGGAAGCCCACCTG CCTCGTGCGGAGGCGGCCCGAGGCCTAGTGACCGGCGCGCGGCGCGGACCCCGGAAGCCCACCTG A C TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:113585073..113585350 26863196 MeRIP-seq:(Medium) rs1177754648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4161,Human_RBP_ID_6260047,Human_RBP_ID_8180297,Human_RBP_ID_9323558,Human_RBP_ID_17834058,Human_RBP_ID_18457561 RMVar_hsa_circ_164972,RMVar_hsa_circ_125311 62745 RMVar_ID_62745 Human_SNP_ID_546257216 m1A Human chr13 - 113585754 113585752 113585755 AAAAATGATTTTTCTGGTAAAAAAAAAAAAAAAAGTAAGGAAAAACAAGAAATAAGTAAGAATGA AAAAATGATTTTTCTGGTAAAAAAAAAAAAA___GTAAGGAAAAACAAGAAATAAGTAAGAATGA CTTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:113585751..113585850 26863410 MeRIP-seq:(Medium) rs113638790 Functional Loss DEL dbSNP153 32..34 33 - - - 62746 RMVar_ID_62746 Human_SNP_ID_546257217 m1A Human chr13 - 113585754 113585752 113585755 AAAAATGATTTTTCTGGTAAAAAAAAAAAAAAAAGTAAGGAAAAACAAGAAATAAGTAAGAATGA AAAAATGATTTTTCTGGTAAAAAAAAAAAAA__AGTAAGGAAAAACAAGAAATAAGTAAGAATGA CTTT CT - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:113585751..113585850 26863410 MeRIP-seq:(Medium) rs113638790 Functional Loss DEL dbSNP153 32..33 33 - - - 62747 RMVar_ID_62747 Human_SNP_ID_546257224 m1A Human chr13 - 113585754 113585754 113585754 AAAAATGATTTTTCTGGTAAAAAAAAAAAAAAAAGTAAGGAAAAACAAGAAATAAGTAAGAATGA AAAAATGATTTTTCTGGTAAAAAAAAAAAAAAGAGTAAGGAAAAACAAGAAATAAGTAAGAATGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:113585751..113585850 26863410 MeRIP-seq:(Medium) rs539424435 Functional Loss SNV dbSNP153 33..33 33 - - - 62748 RMVar_ID_62748 Human_SNP_ID_546258111 m1A Human chr13 - 113588813 113588813 113588813 ACCACTCACTCTCCATCCAATCTACCATCACCACTCACTGTCCCCGAGTCTACCACACTCACTCT ACCACTCACTCTCCATCCAATCTACCATCACCCCTCACTGTCCCCGAGTCTACCACACTCACTCT T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113588522..113589071 26863196 MeRIP-seq:(Medium) rs1008610865 Functional Loss SNV dbSNP153 33..33 33 - - - 62749 RMVar_ID_62749 Human_SNP_ID_546258181 m1A Human chr13 - 113589046 113589046 113589046 TGTGACCCTACATCACCCACTCCAGCACCGCCACTCACTCTCCACCCACAACACCATCACCACAC TGTGACCCTACATCACCCACTCCAGCACCGCCCCTCACTCTCCACCCACAACACCATCACCACAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:113588475..113589166 26863196 MeRIP-seq:(Medium) rs1438950990 Functional Loss SNV dbSNP153 33..33 33 - - - 62750 RMVar_ID_62750 Human_SNP_ID_546261505 m1A Human chr13 - 113600073 113600073 113600073 GTTCTCTCTCATGGTCCTGGAGCCCTACGTGCAAGGATTCTCTCTCACAGTCCTGGGTTCTCTCT GTTCTCTCTCATGGTCCTGGAGCCCTACGTGCCAGGATTCTCTCTCACAGTCCTGGGTTCTCTCT T G lnc-ATP4B-1,lnc-ATP4B-1:2 RNACentral:URS00008BF973,RNACentral:URS00008B5C69 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113599930..113600209 26863196 MeRIP-seq:(Medium) rs868085783 Functional Loss SNV dbSNP153 33..33 33 - - - 62751 RMVar_ID_62751 Human_SNP_ID_546261533 m1A Human chr13 - 113600131 113600131 113600131 GGGTTCTCTCTCACGGCTCTGGAGCCCTACATACAAGGATTCTCTCTCACGGTCCTGGGTTCTCT GGGTTCTCTCTCACGGCTCTGGAGCCCTACATGCAAGGATTCTCTCTCACGGTCCTGGGTTCTCT T C lnc-ATP4B-1,lnc-ATP4B-1:2 RNACentral:URS00008BF973,RNACentral:URS00008B5C69 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113600081..113600157 26863196 MeRIP-seq:(Medium) rs1390852615 Functional Loss SNV dbSNP153 33..33 33 - - - 62752 RMVar_ID_62752 Human_SNP_ID_546261536 m1A Human chr13 + 113600136 113600136 113600136 ACCCAGGACCGTGAGAGAGAATCCTTGTATGTAGGGCTCCAGAGCCGTGAGAGAGAACCCAGGAC ACCCAGGACCGTGAGAGAGAATCCTTGTATGTGGGGCTCCAGAGCCGTGAGAGAGAACCCAGGAC A G TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113599858..113600214 26863196 MeRIP-seq:(Medium) rs185703205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12106263 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62753 RMVar_ID_62753 Human_SNP_ID_546261824 m1A Human chr13 + 113600730 113600728 113600730 AGAATCCTTGCATGTAGGGCTCCAGGACCATGAGAGAGAACCCTCACGTAGGGCTCCAGGACCGC AGAATCCTTGCATGTAGGGCTCCAGGACCAT__GAGAGAACCCTCACGTAGGGCTCCAGGACCGC TGA T TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113600679..113600816 26863196 MeRIP-seq:(Medium) rs1375415685 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12106298 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62754 RMVar_ID_62754 Human_SNP_ID_546261828 m1A Human chr13 + 113600736 113600736 113600736 CTTGCATGTAGGGCTCCAGGACCATGAGAGAGAACCCTCACGTAGGGCTCCAGGACCGCGATAGA CTTGCATGTAGGGCTCCAGGACCATGAGAGAGGACCCTCACGTAGGGCTCCAGGACCGCGATAGA A G TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113600686..113600809 26863196 MeRIP-seq:(Medium) rs904858517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5417592,Human_RBP_ID_12106298 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62755 RMVar_ID_62755 Human_SNP_ID_546262343 m1A Human chr13 + 113602178 113602176 113602179 GGAGGAGTGGACGGAGTTACCCACAGGAGTCGAGGGAGGAGTGGACGGAGTTACCCGCAGGAGCT GGAGGAGTGGACGGAGTTACCCACAGGAGTC___GGAGGAGTGGACGGAGTTACCCGCAGGAGCT CGAG C TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113602130..113602357 26863196 MeRIP-seq:(Medium) rs1294909844 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62756 RMVar_ID_62756 Human_SNP_ID_546262347 m1A Human chr13 + 113602178 113602178 113602178 GGAGGAGTGGACGGAGTTACCCACAGGAGTCGAGGGAGGAGTGGACGGAGTTACCCGCAGGAGCT GGAGGAGTGGACGGAGTTACCCACAGGAGTCGCGGGAGGAGTGGACGGAGTTACCCGCAGGAGCT A C TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113602130..113602357 26863196 MeRIP-seq:(Medium) rs1359274746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62757 RMVar_ID_62757 Human_SNP_ID_546262349 m1A Human chr13 + 113602182 113602182 113602182 GAGTGGACGGAGTTACCCACAGGAGTCGAGGGAGGAGTGGACGGAGTTACCCGCAGGAGCTGAGG GAGTGGACGGAGTTACCCACAGGAGTCGAGGGGGGAGTGGACGGAGTTACCCGCAGGAGCTGAGG A G TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:113601983..113602308 26863196 MeRIP-seq:(Medium) rs1352334131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62758 RMVar_ID_62758 Human_SNP_ID_546263526 m1A Human chr13 + 113606103 113606103 113606103 GGTGATGAGTGTCCATAGGGGATCCTGTGGGAAGGCGGCGTGGTGGTGAGTGTCTGCAGGGGATC GGTGATGAGTGTCCATAGGGGATCCTGTGGGATGGCGGCGTGGTGGTGAGTGTCTGCAGGGGATC A T TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113605796..113606174 26863196 MeRIP-seq:(Medium) rs369740690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8180313,Human_RBP_ID_23586588 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 62759 RMVar_ID_62759 Human_SNP_ID_546268736 m1A Human chr13 - 113623274 113623274 113623274 CGCTCCTGCGGGAGGCTTACCACTTGCTGGGCAATGTTGACATTGGACTGTCCAAAGGTTTTTGG CGCTCCTGCGGGAGGCTTACCACTTGCTGGGCTATGTTGACATTGGACTGTCCAAAGGTTTTTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113623251..113623275 26863196 MeRIP-seq:(Medium) rs550544558 Functional Loss SNV dbSNP153 33..33 33 - - - 62760 RMVar_ID_62760 Human_SNP_ID_546271648 m1A Human chr13 - 113631579 113631579 113631579 AAAGACAATTCAGACAGTCAGTCCCCTCCCACACGGCGAGGGTGCCATGCCCACCATCTGTTCGC AAAGACAATTCAGACAGTCAGTCCCCTCCCACGCGGCGAGGGTGCCATGCCCACCATCTGTTCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113631575..113631704 26863196 MeRIP-seq:(Medium) rs370001344 Functional Loss SNV dbSNP153 33..33 33 - - - 62761 RMVar_ID_62761 Human_SNP_ID_546273110 m1A Human chr13 + 113636076 113636076 113636076 CACCCAACTCAGTCATCCACCTGCCCTTCATCATCGTCAACACCAGCAAGAAGACGGTCATCGAC CACCCAACTCAGTCATCCACCTGCCCTTCATCGTCGTCAACACCAGCAAGAAGACGGTCATCGAC A G TFDP1 Ensembl:ENSG00000198176 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:113636026..113636125 32194978 MeRIP-seq:(Medium) rs1002884470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1805507,Human_RBP_ID_8788507,Human_RBP_ID_9367783,Human_RBP_ID_12106724,Human_RBP_ID_17244031,Human_RBP_ID_17359035,Human_RBP_ID_17475613,Human_RBP_ID_18527683,Human_RBP_ID_26324476,Human_RBP_ID_26807600,Human_RBP_ID_26913977,Human_RBP_ID_27426816 Human_Splice_Rec_1486024,Human_Splice_Rec_1486025,Human_Splice_Rec_1486044,Human_Splice_Rec_1486045,Human_Splice_Rec_1486066 Human_miRNA_ID_2052001,Human_miRNA_ID_2052002 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164976,RMVar_hsa_circ_124245,RMVar_hsa_circ_164973,RMVar_hsa_circ_337273,RMVar_hsa_circ_113492,RMVar_hsa_circ_164974,RMVar_hsa_circ_164975,RMVar_hsa_circ_16737,RMVar_hsa_circ_164980,RMVar_hsa_circ_21209,RMVar_hsa_circ_329252,RMVar_hsa_circ_349648,RMVar_hsa_circ_118145,RMVar_hsa_circ_164981,RMVar_hsa_circ_164982,RMVar_hsa_circ_73403,RMVar_hsa_circ_324443,RMVar_hsa_circ_348585,RMVar_hsa_circ_101068,RMVar_hsa_circ_96432,RMVar_hsa_circ_164983,RMVar_hsa_circ_164984 62762 RMVar_ID_62762 Human_SNP_ID_546273407 m1A Human chr13 - 113636871 113636871 113636871 AGTGGGTCACGGCACTGGCTGGACCCCACCCCAGCCACACCCCTGCCCTCATCCCCCTCACAGCC AGTGGGTCACGGCACTGGCTGGACCCCACCCCCGCCACACCCCTGCCCTCATCCCCCTCACAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113636868..113636984 26863196 MeRIP-seq:(Medium) rs1566679265 Functional Loss SNV dbSNP153 33..33 33 - - - 62763 RMVar_ID_62763 Human_SNP_ID_546323846 m1A Human chr13 - 113838170 113838160 113838170 CTTGTTCCCAGATGTCAACGAATGCAGCCAGGAGAACGGGGGCTGCCTCCAGATCTGCCACAACA CTTGTTCCCAGATGTCAACGAATGCAGCCAGG__________CTGCCTCCAGATCTGCCACAACA GCCCCCGTTCT G GAS6 Ensembl:ENSG00000183087 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:113838121..113847719 32194978 MeRIP-seq:(Medium) rs1566364816 Functional Loss DEL dbSNP153 33..42 33 - - - Human_Splice_Rec_1486188 RMVar_hsa_circ_32208,RMVar_hsa_circ_52703,RMVar_hsa_circ_8628,RMVar_hsa_circ_95029,RMVar_hsa_circ_326499,RMVar_hsa_circ_124084,RMVar_hsa_circ_164993,RMVar_hsa_circ_164991,RMVar_hsa_circ_164992,RMVar_hsa_circ_284952,RMVar_hsa_circ_326583,RMVar_hsa_circ_284372,RMVar_hsa_circ_292649,RMVar_hsa_circ_100918,RMVar_hsa_circ_164994,RMVar_hsa_circ_164995,RMVar_hsa_circ_164996 62764 RMVar_ID_62764 Human_SNP_ID_546323907 m1A Human chr13 + 113838302 113838302 113838302 CACAGCCCAGCCCTGGAGCAGGGAGGGAGCCCAGAGGTGCACAGCCCAGCCCTGGAGCAGAGAGA CACAGCCCAGCCCTGGAGCAGGGAGGGAGCCCGGAGGTGCACAGCCCAGCCCTGGAGCAGAGAGA A G GAS6-AS1 Ensembl:ENSG00000233695 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113837924..113838563 26863196 MeRIP-seq:(Medium) rs1398935552 Functional Loss SNV dbSNP153 33..33 33 - - - 62765 RMVar_ID_62765 Human_SNP_ID_546324088 m1A Human chr13 - 113838748 113838748 113838748 TCCCTTCCTCCTGCTCCAGTGCTGGGCTGTGCACCCCCCCGGCTCCTTCCCTGCTCCAGTGCTGG TCCCTTCCTCCTGCTCCAGTGCTGGGCTGTGCCCCCCCCCGGCTCCTTCCCTGCTCCAGTGCTGG T G GAS6 Ensembl:ENSG00000183087 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113838699..113838788 26863196 MeRIP-seq:(Medium) rs1237153955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22472896 RMVar_hsa_circ_32208,RMVar_hsa_circ_52703,RMVar_hsa_circ_8628,RMVar_hsa_circ_95029,RMVar_hsa_circ_326499,RMVar_hsa_circ_124084,RMVar_hsa_circ_164991,RMVar_hsa_circ_164992,RMVar_hsa_circ_326583,RMVar_hsa_circ_284372,RMVar_hsa_circ_292649,RMVar_hsa_circ_164995,RMVar_hsa_circ_164996 62766 RMVar_ID_62766 Human_SNP_ID_546324882 m1A Human chr13 - 113841348 113841348 113841348 GAAGCCAGTGTGGTTGGGCAGCTTCCCCAAGAAGCCTGGGACTCGTAGCCAGGGCCTCTGGTGAG GAAGCCAGTGTGGTTGGGCAGCTTCCCCAAGATGCCTGGGACTCGTAGCCAGGGCCTCTGGTGAG T A GAS6 Ensembl:ENSG00000183087 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:113841298..113841437 26863196 MeRIP-seq:(Medium) rs1030219419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52703,RMVar_hsa_circ_8628,RMVar_hsa_circ_326499,RMVar_hsa_circ_124084,RMVar_hsa_circ_164992,RMVar_hsa_circ_284372,RMVar_hsa_circ_164996,RMVar_hsa_circ_24263 62767 RMVar_ID_62767 Human_SNP_ID_546324944 m1A Human chr13 - 113841484 113841484 113841484 GAAACTGTGGGGCGTATGGAGGAAATTGAGGCATATGGAGGAAACTGGGGCATACGGAGGAAACG GAAACTGTGGGGCGTATGGAGGAAATTGAGGCGTATGGAGGAAACTGGGGCATACGGAGGAAACG T C GAS6 Ensembl:ENSG00000183087 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113841435..113841595 26863196 MeRIP-seq:(Medium) rs902597535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52703,RMVar_hsa_circ_8628,RMVar_hsa_circ_326499,RMVar_hsa_circ_124084,RMVar_hsa_circ_164992,RMVar_hsa_circ_284372,RMVar_hsa_circ_164996,RMVar_hsa_circ_24263 62768 RMVar_ID_62768 Human_SNP_ID_546327821 m1A Human chr13 - 113851136 113851132 113851137 GTCCATCCTCATTCATTTATCCATCCATCTCCATTCATTTACTCATCCACCCACTCATTCATTCT GTCCATCCTCATTCATTTATCCATCCATCTC_____ATTTACTCATCCACCCACTCATTCATTCT TGAATG T GAS6 Ensembl:ENSG00000183087 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:113851128..113851317 26863196 MeRIP-seq:(Medium) rs527471729 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_196301,Human_RBP_ID_2376218,Human_RBP_ID_26807610 RMVar_hsa_circ_124084,RMVar_hsa_circ_164992 62769 RMVar_ID_62769 Human_SNP_ID_546356343 m1A Human chr13 + 113955908 113955888 113955908 GGAGCATCCGGTGGAGAGGAGGAGCATCTCGCAGAGAGGAGGAGCATCTCGCGGAGACGAGGAGC GGAGCATCCGGTG____________________GAGAGGAGGAGCATCTCGCGGAGACGAGGAGC GGAGAGGAGGAGCATCTCGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113955858..113955939 26863196 MeRIP-seq:(Medium) rs1282165555 Functional Loss DEL dbSNP153 14..33 33 - - - 62770 RMVar_ID_62770 Human_SNP_ID_546356353 m1A Human chr13 + 113955908 113955908 113955908 GGAGCATCCGGTGGAGAGGAGGAGCATCTCGCAGAGAGGAGGAGCATCTCGCGGAGACGAGGAGC GGAGCATCCGGTGGAGAGGAGGAGCATCTCGCGGAGAGGAGGAGCATCTCGCGGAGACGAGGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113955858..113955939 26863196 MeRIP-seq:(Medium) rs1446790253 Functional Loss SNV dbSNP153 33..33 33 - - - 62771 RMVar_ID_62771 Human_SNP_ID_546356589 m1A Human chr13 + 113956299 113956297 113956299 CCGGTGGAGAGGAGGAGCATCTGGTGGAGACGAGGAGCATCTGGTGGAGAGGAGGAGTAGTATCT CCGGTGGAGAGGAGGAGCATCTGGTGGAGAC__GGAGCATCTGGTGGAGAGGAGGAGTAGTATCT CGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113956278..113956346 26863196 MeRIP-seq:(Medium) rs1261203680 Functional Loss DEL dbSNP153 32..33 33 - - - 62772 RMVar_ID_62772 Human_SNP_ID_546358450 m1A Human chr13 - 113963337 113963337 113963337 GCTGAGGACGGGCCGAGGCTGAGGACGGGGCGAGGGCTGAGGACAGGGACCGAGGCTGAGGACAG GCTGAGGACGGGCCGAGGCTGAGGACGGGGCGGGGGCTGAGGACAGGGACCGAGGCTGAGGACAG T C C13orf46 Ensembl:ENSG00000283199 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113963305..113963415 26863196 MeRIP-seq:(Medium) rs1303187936 Functional Loss SNV dbSNP153 33..33 33 - - - 62773 RMVar_ID_62773 Human_SNP_ID_546358469 m1A Human chr13 - 113963373 113963356 113963373 AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGAGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG AGGCTGAGGACAGGGGCGAGGCTGAGGACGGG_________________CGAGGCTGAGGACGGG GGCCCGTCCTCAGCCTCT G C13orf46 Ensembl:ENSG00000283199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113963194..113963631 26863196 MeRIP-seq:(Medium) rs1566419065 Functional Loss DEL dbSNP153 33..49 33 - - - 62774 RMVar_ID_62774 Human_SNP_ID_546358478 m1A Human chr13 - 113963373 113963373 113963373 AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGAGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGTGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG T A C13orf46 Ensembl:ENSG00000283199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113963194..113963631 26863196 MeRIP-seq:(Medium) rs1258004634 Functional Loss SNV dbSNP153 33..33 33 - - - 62775 RMVar_ID_62775 Human_SNP_ID_546358479 m1A Human chr13 - 113963373 113963373 113963373 AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGAGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGGGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG T C C13orf46 Ensembl:ENSG00000283199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113963194..113963631 26863196 MeRIP-seq:(Medium) rs1258004634 Functional Loss SNV dbSNP153 33..33 33 - - - 62776 RMVar_ID_62776 Human_SNP_ID_546358480 m1A Human chr13 - 113963373 113963373 113963373 AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGAGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG AGGCTGAGGACAGGGGCGAGGCTGAGGACGGGCGAGGCTGAGGACGGGCCGAGGCTGAGGACGGG T G C13orf46 Ensembl:ENSG00000283199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113963194..113963631 26863196 MeRIP-seq:(Medium) rs1258004634 Functional Loss SNV dbSNP153 33..33 33 - - - 62777 RMVar_ID_62777 Human_SNP_ID_546363517 m1A Human chr13 - 113979891 113979872 113979891 GTAGGCACGTAGGAGGAGGTGCACACACATGGAGGTAGTGGACACACATGGCAGGAGGTGCACAC GTAGGCACGTAGGAGGAGGTGCACACACATGG___________________CAGGAGGTGCACAC GCCATGTGTGTCCACTACCT G RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113979889..113980432 26863196 MeRIP-seq:(Medium) rs916116363 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_9417402 62778 RMVar_ID_62778 Human_SNP_ID_546365193 m1A Human chr13 - 113984690 113984686 113984690 GGATGGACAGGGTGAGTGATGGGTGGATAGACAGATGGATGAGTGATGGGTGGATGGAAGGATGG GGATGGACAGGGTGAGTGATGGGTGGATAGAC____GGATGAGTGATGGGTGGATGGAAGGATGG CATCT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113984651..113984771 26863196 MeRIP-seq:(Medium) rs1408006733 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5175258 62779 RMVar_ID_62779 Human_SNP_ID_546365194 m1A Human chr13 - 113984690 113984690 113984690 GGATGGACAGGGTGAGTGATGGGTGGATAGACAGATGGATGAGTGATGGGTGGATGGAAGGATGG GGATGGACAGGGTGAGTGATGGGTGGATAGACTGATGGATGAGTGATGGGTGGATGGAAGGATGG T A RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113984651..113984771 26863196 MeRIP-seq:(Medium) rs1390248071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5175258 62780 RMVar_ID_62780 Human_SNP_ID_546365479 m1A Human chr13 - 113988947 113988946 113988947 GTACGGACAGGGTGAGTGATGGGTGTACGGACAGGGTGAGTGATGGGTGGATGGACAGATGGGCG GTACGGACAGGGTGAGTGATGGGTGTACGGAC_GGGTGAGTGATGGGTGGATGGACAGATGGGCG CT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113988915..113989114 26863196 MeRIP-seq:(Medium) rs1483904254 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3438934,Human_RBP_ID_5645558 62781 RMVar_ID_62781 Human_SNP_ID_546365480 m1A Human chr13 - 113988947 113988947 113988947 GTACGGACAGGGTGAGTGATGGGTGTACGGACAGGGTGAGTGATGGGTGGATGGACAGATGGGCG GTACGGACAGGGTGAGTGATGGGTGTACGGACGGGGTGAGTGATGGGTGGATGGACAGATGGGCG T C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113988915..113989114 26863196 MeRIP-seq:(Medium) rs544022978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3438934,Human_RBP_ID_5645558 62782 RMVar_ID_62782 Human_SNP_ID_546365531 m1A Human chr13 + 113989063 113989063 113989063 TCCACCCATCACTCACCCATCTGTCCATCACCATCACTCACCCATCTGTCAGTCCACCGATCACT TCCACCCATCACTCACCCATCTGTCCATCACCGTCACTCACCCATCTGTCAGTCCACCGATCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113988817..113989851 26863196 MeRIP-seq:(Medium) rs1418536711 Functional Loss SNV dbSNP153 33..33 33 - - - 62783 RMVar_ID_62783 Human_SNP_ID_546365532 m1A Human chr13 + 113989063 113989063 113989063 TCCACCCATCACTCACCCATCTGTCCATCACCATCACTCACCCATCTGTCAGTCCACCGATCACT TCCACCCATCACTCACCCATCTGTCCATCACCTTCACTCACCCATCTGTCAGTCCACCGATCACT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113988817..113989851 26863196 MeRIP-seq:(Medium) rs1418536711 Functional Loss SNV dbSNP153 33..33 33 - - - 62784 RMVar_ID_62784 Human_SNP_ID_546365533 m1A Human chr13 + 113989074 113989074 113989074 CTCACCCATCTGTCCATCACCATCACTCACCCATCTGTCAGTCCACCGATCACTCACCCATCTGT CTCACCCATCTGTCCATCACCATCACTCACCCGTCTGTCAGTCCACCGATCACTCACCCATCTGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:113988815..113989752 26863196 MeRIP-seq:(Medium) rs1205562425 Functional Loss SNV dbSNP153 33..33 33 - - - 62785 RMVar_ID_62785 Human_SNP_ID_546365603 m1A Human chr13 - 113989275 113989264 113989275 GGGTGAGTAATGGGTGGATGGACGGATGGGTGAGTGATGGGTGGATGGACAGATGGGTGAGAGAT GGGTGAGTAATGGGTGGATGGACGGATGGGTG___________GATGGACAGATGGGTGAGAGAT CCACCCATCACT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:113989065..113989486 26863196 MeRIP-seq:(Medium) rs1448096674 Functional Loss DEL dbSNP153 33..43 33 - - - 62786 RMVar_ID_62786 Human_SNP_ID_546371498 m1A Human chr13 - 114005774 114005773 114005775 AAGGTGGTGTCCGGCAGGGCAGGAGGGGGGAGAAGGGTAAGGTGGCATCCGGCAGGGCCGGAGGG AAGGTGGTGTCCGGCAGGGCAGGAGGGGGGA__AGGGTAAGGTGGCATCCGGCAGGGCCGGAGGG TTC T RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:114005668..114005815 26863196 MeRIP-seq:(Medium) rs1238321399 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3438948,Human_RBP_ID_8180417,Human_RBP_ID_9323583,Human_RBP_ID_9417404 RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_165001 62787 RMVar_ID_62787 Human_SNP_ID_546371500 m1A Human chr13 - 114005776 114005775 114005776 GTAAGGTGGTGTCCGGCAGGGCAGGAGGGGGGAGAAGGGTAAGGTGGCATCCGGCAGGGCCGGAG GTAAGGTGGTGTCCGGCAGGGCAGGAGGGGGG_GAAGGGTAAGGTGGCATCCGGCAGGGCCGGAG CT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114005695..114005815 26863196 MeRIP-seq:(Medium) rs1468434579 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3438948,Human_RBP_ID_9323583,Human_RBP_ID_9417404 RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_165001 62788 RMVar_ID_62788 Human_SNP_ID_546373229 m1A Human chr13 + 114010792 114010792 114010792 GGAGGTGGGGAGGAGGGGGCCGCGTGGGGAGGAGGGGGCCGCGAGGGGAGTAGGGGGCTGCGTGA GGAGGTGGGGAGGAGGGGGCCGCGTGGGGAGGGGGGGGCCGCGAGGGGAGTAGGGGGCTGCGTGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:114010773..114011100 26863196 MeRIP-seq:(Medium) rs917690765 Functional Loss SNV dbSNP153 33..33 33 - - - 62789 RMVar_ID_62789 Human_SNP_ID_546373261 m1A Human chr13 - 114010818 114010818 114010818 GGCGTTGCGGTGCTGGAGGCTCCTCGTCACGCAGCCCCCTACTCCCCTCGCGGCCCCCTCCTCCC GGCGTTGCGGTGCTGGAGGCTCCTCGTCACGCGGCCCCCTACTCCCCTCGCGGCCCCCTCCTCCC T C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:114010768..114010935 32194978 MeRIP-seq:(Medium) rs759834601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919 62790 RMVar_ID_62790 Human_SNP_ID_546373753 m1A Human chr13 + 114012240 114012240 114012240 TGCTTTTGTGACACTGTCTCGACTCCCCCAGAACGTACACAGCTTAAATAGGTCGGTGAACCACC TGCTTTTGTGACACTGTCTCGACTCCCCCAGAGCGTACACAGCTTAAATAGGTCGGTGAACCACC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:114012237..114012435 26863196 MeRIP-seq:(Medium) rs563398219 Functional Loss SNV dbSNP153 33..33 33 - - - 62791 RMVar_ID_62791 Human_SNP_ID_546373914 m1A Human chr13 + 114012635 114012631 114012635 CACGCACACTCCCCACTCACTCCTCATTCCACACACACTCCCCATTCCACACGCCTTCCACACTC CACGCACACTCCCCACTCACTCCTCATTC____CACACTCCCCATTCCACACGCCTTCCACACTC CCACA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:114012532..114012752 26863196 MeRIP-seq:(Medium) rs1293439319 Functional Loss DEL dbSNP153 30..33 33 - - - 62792 RMVar_ID_62792 Human_SNP_ID_546373915 m1A Human chr13 + 114012635 114012631 114012635 CACGCACACTCCCCACTCACTCCTCATTCCACACACACTCCCCATTCCACACGCCTTCCACACTC CACGCACACTCCCCACTCACTCCTCATTCCA__CACACTCCCCATTCCACACGCCTTCCACACTC CCACA CCA - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:114012532..114012752 26863196 MeRIP-seq:(Medium) rs1293439319 Functional Loss DEL dbSNP153 32..33 33 - - - 62793 RMVar_ID_62793 Human_SNP_ID_546373923 m1A Human chr13 + 114012673 114012669 114012673 TCCCCATTCCACACGCCTTCCACACTCCCCACACACTGTCCACGCACTCCACACACTCCTCATTC TCCCCATTCCACACGCCTTCCACACTCCC____CACTGTCCACGCACTCCACACACTCCTCATTC CCACA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114012667..114012738 26863196 MeRIP-seq:(Medium) rs141522015 Functional Loss DEL dbSNP153 30..33 33 - - - GWAS_ID_7675,GWAS_ID_7676,GWAS_ID_7677,GWAS_ID_7678,GWAS_ID_7679,GWAS_ID_7680,GWAS_ID_7681,GWAS_ID_7682,GWAS_ID_7683,GWAS_ID_7684 62794 RMVar_ID_62794 Human_SNP_ID_546373924 m1A Human chr13 + 114012673 114012669 114012673 TCCCCATTCCACACGCCTTCCACACTCCCCACACACTGTCCACGCACTCCACACACTCCTCATTC TCCCCATTCCACACGCCTTCCACACTCCCCA__CACTGTCCACGCACTCCACACACTCCTCATTC CCACA CCA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114012667..114012738 26863196 MeRIP-seq:(Medium) rs141522015 Functional Loss DEL dbSNP153 32..33 33 - - - GWAS_ID_7675,GWAS_ID_7676,GWAS_ID_7677,GWAS_ID_7678,GWAS_ID_7679,GWAS_ID_7680,GWAS_ID_7681,GWAS_ID_7682,GWAS_ID_7683,GWAS_ID_7684 62795 RMVar_ID_62795 Human_SNP_ID_546373926 m1A Human chr13 + 114012673 114012673 114012673 TCCCCATTCCACACGCCTTCCACACTCCCCACACACTGTCCACGCACTCCACACACTCCTCATTC TCCCCATTCCACACGCCTTCCACACTCCCCACGCACTGTCCACGCACTCCACACACTCCTCATTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114012667..114012738 26863196 MeRIP-seq:(Medium) rs1241091233 Functional Loss SNV dbSNP153 33..33 33 - - - 62796 RMVar_ID_62796 Human_SNP_ID_546374285 m1A Human chr13 - 114013444 114013436 114013444 AGAGACAGGGAGAGAGACAAAGGGGGAGAGACAGAGAGATGGAGAGAGAGAGGGAAACAGAGAGA AGAGACAGGGAGAGAGACAAAGGGGGAGAGAC________GGAGAGAGAGAGGGAAACAGAGAGA CATCTCTCT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:114013440..114014184 26863196 MeRIP-seq:(Medium) rs1408297812 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_5350667 RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62797 RMVar_ID_62797 Human_SNP_ID_546374292 m1A Human chr13 - 114013444 114013443 114013445 AGAGACAGGGAGAGAGACAAAGGGGGAGAGACAGAGAGATGGAGAGAGAGAGGGAAACAGAGAGA AGAGACAGGGAGAGAGACAAAGGGGGAGAGA__GAGAGATGGAGAGAGAGAGGGAAACAGAGAGA CTG C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:114013440..114014184 26863196 MeRIP-seq:(Medium) rs1412360679 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5350667 RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62798 RMVar_ID_62798 Human_SNP_ID_546374598 m1A Human chr13 + 114013797 114013797 114013797 TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTAACTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTACCTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:114013380..114013874;chr13:114013398..114014241 26863196 MeRIP-seq:(Medium) rs111173930 Functional Loss SNV dbSNP153 33..33 33 - - - 62799 RMVar_ID_62799 Human_SNP_ID_546374599 m1A Human chr13 + 114013797 114013797 114013797 TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTAACTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTAGCTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:114013380..114013874;chr13:114013398..114014241 26863196 MeRIP-seq:(Medium) rs111173930 Functional Loss SNV dbSNP153 33..33 33 - - - 62800 RMVar_ID_62800 Human_SNP_ID_546374600 m1A Human chr13 + 114013797 114013797 114013797 TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTAACTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC TCTGTCTCTCTCCCTCTCTGTCTCTCTCCCTATCTCCATCTCTCTCTCCCCGTCTCTTTCTCTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:114013380..114013874;chr13:114013398..114014241 26863196 MeRIP-seq:(Medium) rs111173930 Functional Loss SNV dbSNP153 33..33 33 - - - 62801 RMVar_ID_62801 Human_SNP_ID_546374804 m1A Human chr13 - 114013947 114013944 114013948 ATCGAGACGGAGAGAGAGAGAGAGAGACAGAGAGATAGAGACAGGGAGAGAGAGACGGAGAGAGA ATCGAGACGGAGAGAGAGAGAGAGAGACAGA____TAGAGACAGGGAGAGAGAGACGGAGAGAGA ATCTC A RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114013944..114014116 26863196 MeRIP-seq:(Medium) rs1302103861 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62802 RMVar_ID_62802 Human_SNP_ID_546374805 m1A Human chr13 - 114013947 114013944 114013948 ATCGAGACGGAGAGAGAGAGAGAGAGACAGAGAGATAGAGACAGGGAGAGAGAGACGGAGAGAGA ATCGAGACGGAGAGAGAGAGAGAGAGACAGA__GATAGAGACAGGGAGAGAGAGACGGAGAGAGA ATCTC ATC RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114013944..114014116 26863196 MeRIP-seq:(Medium) rs1302103861 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62803 RMVar_ID_62803 Human_SNP_ID_546374919 m1A Human chr13 - 114014061 114014056 114014061 AGAGAGAGGCAGAGACAGACGGAGAGAGAGGCAGAGACAGACGGAGAGAGAGATAGAGACGGAGA AGAGAGAGGCAGAGACAGACGGAGAGAGAGGC_____CAGACGGAGAGAGAGATAGAGACGGAGA GTCTCT G RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114013927..114014221 26863196 MeRIP-seq:(Medium) rs1284001844 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62804 RMVar_ID_62804 Human_SNP_ID_546375357 m1A Human chr13 - 114015260 114015258 114015260 TCACTGAGTCTGGGGTGAGCTGCCCGACCGTCATGTGTGACATCTTCTTCTCCCTCCGGGAGGCG TCACTGAGTCTGGGGTGAGCTGCCCGACCGTC__GTGTGACATCTTCTTCTCCCTCCGGGAGGCG CAT C RASA3 Ensembl:ENSG00000185989 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114015163..114015351 26863196 MeRIP-seq:(Medium) rs1279166659 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18637217 Human_Splice_Rec_1486364,Human_Splice_Rec_1486365 Human_miRNA_ID_2540084 RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62805 RMVar_ID_62805 Human_SNP_ID_546375359 m1A Human chr13 - 114015260 114015260 114015260 TCACTGAGTCTGGGGTGAGCTGCCCGACCGTCATGTGTGACATCTTCTTCTCCCTCCGGGAGGCG TCACTGAGTCTGGGGTGAGCTGCCCGACCGTCCTGTGTGACATCTTCTTCTCCCTCCGGGAGGCG T G RASA3 Ensembl:ENSG00000185989 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114015163..114015351 26863196 MeRIP-seq:(Medium) rs747411335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18637217 Human_Splice_Rec_1486364,Human_Splice_Rec_1486365 Human_miRNA_ID_2540084 RMVar_hsa_circ_4392,RMVar_hsa_circ_61745,RMVar_hsa_circ_19922,RMVar_hsa_circ_78744,RMVar_hsa_circ_112626,RMVar_hsa_circ_165001,RMVar_hsa_circ_12325,RMVar_hsa_circ_18824,RMVar_hsa_circ_165002,RMVar_hsa_circ_11445,RMVar_hsa_circ_50919,RMVar_hsa_circ_30061,RMVar_hsa_circ_23605,RMVar_hsa_circ_79513,RMVar_hsa_circ_165004 62806 RMVar_ID_62806 Human_SNP_ID_546381802 m1A Human chr13 - 114032719 114032719 114032719 GTGGGGGTGCCATGGAACGTGGTGTCAAGTGTAGGGGTGCCGTGGGACGTGTTGTCAGTGTGGGG GTGGGGGTGCCATGGAACGTGGTGTCAAGTGTGGGGGTGCCGTGGGACGTGTTGTCAGTGTGGGG T C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114032685..114032772 26863196 MeRIP-seq:(Medium) rs1306907300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8075405 RMVar_hsa_circ_61745,RMVar_hsa_circ_12325,RMVar_hsa_circ_31129,RMVar_hsa_circ_365246,RMVar_hsa_circ_35384,RMVar_hsa_circ_331264,RMVar_hsa_circ_318370,RMVar_hsa_circ_346291 62807 RMVar_ID_62807 Human_SNP_ID_546382100 m1A Human chr13 - 114033407 114033407 114033407 GGTGTCAGTGTGGGGGTGCCGTGGAACATGGTATGAAGTGTGGGGGTGCCATGGAACGTGGTGTC GGTGTCAGTGTGGGGGTGCCGTGGAACATGGTGTGAAGTGTGGGGGTGCCATGGAACGTGGTGTC T C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:114033134..114033454 26863196 MeRIP-seq:(Medium) rs1460353830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8075407 RMVar_hsa_circ_61745,RMVar_hsa_circ_12325,RMVar_hsa_circ_31129,RMVar_hsa_circ_365246,RMVar_hsa_circ_35384,RMVar_hsa_circ_331264,RMVar_hsa_circ_318370,RMVar_hsa_circ_346291 62808 RMVar_ID_62808 Human_SNP_ID_546402301 m1A Human chr13 + 114098630 114098630 114098630 CCCAACAAGATGTAGGAAACCCCATGGCCGGGATGAGGGGAGGCAGGAAGGGCAAGGGGCATGGA CCCAACAAGATGTAGGAAACCCCATGGCCGGGGTGAGGGGAGGCAGGAAGGGCAAGGGGCATGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:114098624..114098741 32194978 MeRIP-seq:(Medium) rs1221361999 Functional Loss SNV dbSNP153 33..33 33 - - - 62809 RMVar_ID_62809 Human_SNP_ID_546404902 m1A Human chr13 + 114103973 114103973 114103973 CAGCCACGGACACCCACCCCCGATGCGTCCACACTGCCGCCGGCCACAGACACCCACCCCTGATG CAGCCACGGACACCCACCCCCGATGCGTCCACGCTGCCGCCGGCCACAGACACCCACCCCTGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114103971..114104042 26863196 MeRIP-seq:(Medium) rs58190592 Functional Loss SNV dbSNP153 33..33 33 - - - 62810 RMVar_ID_62810 Human_SNP_ID_546405064 m1A Human chr13 + 114104310 114104310 114104310 TGCGTCCACGCTGTCCCCGGCCACGGACACCCACCCCCGATGCGTCCACACTGCCGCCGGCCACG TGCGTCCACGCTGTCCCCGGCCACGGACACCCCCCCCCGATGCGTCCACACTGCCGCCGGCCACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114104302..114104406 26863196 MeRIP-seq:(Medium) rs1000543555 Functional Loss SNV dbSNP153 33..33 33 - - - 62811 RMVar_ID_62811 Human_SNP_ID_546406172 m1A Human chr13 - 114108287 114108287 114108287 ATGGTTTCAGGGTGACAGACATGGGGTGACGGACGGGGATGACAGACACGGGGTGACGGATGCAG ATGGTTTCAGGGTGACAGACATGGGGTGACGGTCGGGGATGACAGACACGGGGTGACGGATGCAG T A RASA3-IT1,RASA3 Ensembl:ENSG00000232487,Ensembl:ENSG00000185989 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:114108173..114108541 26863196 MeRIP-seq:(Medium) rs1460288501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260595 62812 RMVar_ID_62812 Human_SNP_ID_546409695 m1A Human chr13 - 114119696 114119693 114119696 GGGCCCTGATCGACGCCTGGCTGGAGAGAGGGAGGGGGGGCCCTGATCGACGCCTGGCTGGAGAG GGGCCCTGATCGACGCCTGGCTGGAGAGAGGG___GGGGGCCCTGATCGACGCCTGGCTGGAGAG CCCT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114119689..114119760 26863196 MeRIP-seq:(Medium) rs1459550848 Functional Loss DEL dbSNP153 33..35 33 - - - 62813 RMVar_ID_62813 Human_SNP_ID_546409696 m1A Human chr13 - 114119696 114119694 114119696 GGGCCCTGATCGACGCCTGGCTGGAGAGAGGGAGGGGGGGCCCTGATCGACGCCTGGCTGGAGAG GGGCCCTGATCGACGCCTGGCTGGAGAGAGGG__GGGGGGCCCTGATCGACGCCTGGCTGGAGAG CCT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114119689..114119760 26863196 MeRIP-seq:(Medium) rs1277357734 Functional Loss DEL dbSNP153 33..34 33 - - - 62814 RMVar_ID_62814 Human_SNP_ID_546409697 m1A Human chr13 - 114119696 114119695 114119696 GGGCCCTGATCGACGCCTGGCTGGAGAGAGGGAGGGGGGGCCCTGATCGACGCCTGGCTGGAGAG GGGCCCTGATCGACGCCTGGCTGGAGAGAGGG_GGGGGGGCCCTGATCGACGCCTGGCTGGAGAG CT C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114119689..114119760 26863196 MeRIP-seq:(Medium) rs1219414152 Functional Loss DEL dbSNP153 33..33 33 - - - 62815 RMVar_ID_62815 Human_SNP_ID_546409700 m1A Human chr13 - 114119696 114119696 114119696 GGGCCCTGATCGACGCCTGGCTGGAGAGAGGGAGGGGGGGCCCTGATCGACGCCTGGCTGGAGAG GGGCCCTGATCGACGCCTGGCTGGAGAGAGGGGGGGGGGGCCCTGATCGACGCCTGGCTGGAGAG T C RASA3 Ensembl:ENSG00000185989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114119689..114119760 26863196 MeRIP-seq:(Medium) rs1346764388 Functional Loss SNV dbSNP153 33..33 33 - - - 62816 RMVar_ID_62816 Human_SNP_ID_546440941 m1A Human chr13 + 114234997 114234996 114234997 CGAGTCCTGGGGCGGCGGCGGCGGCTGCAGGCACGGGCACGGGCACGGGGCGGGGTGCTTAGGGT CGAGTCCTGGGGCGGCGGCGGCGGCTGCAGGC_CGGGCACGGGCACGGGGCGGGGTGCTTAGGGT CA C CDC16 Ensembl:ENSG00000130177 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:114234901..114235100 26863196 MeRIP-seq:(Medium) rs1276299496 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4264523,Human_RBP_ID_5087549,Human_RBP_ID_8230272,Human_RBP_ID_8940971,Human_RBP_ID_9417282,Human_RBP_ID_18417755,Human_RBP_ID_21968568 62817 RMVar_ID_62817 Human_SNP_ID_546440942 m1A Human chr13 + 114234997 114234997 114234997 CGAGTCCTGGGGCGGCGGCGGCGGCTGCAGGCACGGGCACGGGCACGGGGCGGGGTGCTTAGGGT CGAGTCCTGGGGCGGCGGCGGCGGCTGCAGGCGCGGGCACGGGCACGGGGCGGGGTGCTTAGGGT A G CDC16 Ensembl:ENSG00000130177 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:114234901..114235100 26863196 MeRIP-seq:(Medium) rs1205533153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4264523,Human_RBP_ID_5087549,Human_RBP_ID_8230272,Human_RBP_ID_8940971,Human_RBP_ID_9417282,Human_RBP_ID_18417755,Human_RBP_ID_21968568 62818 RMVar_ID_62818 Human_SNP_ID_546440963 m1A Human chr13 - 114235020 114235020 114235020 GCCGCTAGGCGCGCGCCTCCTGCACCCTAAGCACCCCGCCCCGTGCCCGTGCCCGTGCCTGCAGC GCCGCTAGGCGCGCGCCTCCTGCACCCTAAGCGCCCCGCCCCGTGCCCGTGCCCGTGCCTGCAGC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:114234934..114235024 26863410 MeRIP-seq:(Medium) rs540239709 Functional Loss SNV dbSNP153 33..33 33 - - - 62819 RMVar_ID_62819 Human_SNP_ID_546440964 m1A Human chr13 + 114235025 114235025 114235025 AGGCACGGGCACGGGCACGGGGCGGGGTGCTTAGGGTGCAGGAGGCGCGCGCCTAGCGGCGGAGT AGGCACGGGCACGGGCACGGGGCGGGGTGCTTCGGGTGCAGGAGGCGCGCGCCTAGCGGCGGAGT A C CDC16 Ensembl:ENSG00000130177 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr13:114234890..114235165;chr13:114234901..114236875 26863196 MeRIP-seq:(Medium) rs961868256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230605,Human_RBP_ID_756357,Human_RBP_ID_3944188,Human_RBP_ID_4264525,Human_RBP_ID_5087549,Human_RBP_ID_8940971,Human_RBP_ID_9323586,Human_RBP_ID_9417282,Human_RBP_ID_18417756,Human_RBP_ID_18936257,Human_RBP_ID_21968569,Human_RBP_ID_26324240,Human_RBP_ID_26914015,Human_RBP_ID_27808071 62820 RMVar_ID_62820 Human_SNP_ID_546440967 m1A Human chr13 + 114235032 114235032 114235032 GGCACGGGCACGGGGCGGGGTGCTTAGGGTGCAGGAGGCGCGCGCCTAGCGGCGGAGTGTGGCGT GGCACGGGCACGGGGCGGGGTGCTTAGGGTGCCGGAGGCGCGCGCCTAGCGGCGGAGTGTGGCGT A C CDC16 Ensembl:ENSG00000130177 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr13:114234901..114235186;chr13:114234935..114235075 26863196 MeRIP-seq:(Medium) rs187234058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230605,Human_RBP_ID_756357,Human_RBP_ID_3944188,Human_RBP_ID_4276704,Human_RBP_ID_5087549,Human_RBP_ID_8940971,Human_RBP_ID_9323586,Human_RBP_ID_9417282,Human_RBP_ID_18417756,Human_RBP_ID_18936257,Human_RBP_ID_21968569,Human_RBP_ID_26324240,Human_RBP_ID_27808071 62821 RMVar_ID_62821 Human_SNP_ID_546453841 m1A Human chr13 + 114281651 114281651 114281651 CGGCTCGGCGGAGAGTGCGGCATGCGCTCGGAAAAGGAGGGGGCCGGAGGCCTTCGGGCGGCCGT CGGCTCGGCGGAGAGTGCGGCATGCGCTCGGAGAAGGAGGGGGCCGGAGGCCTTCGGGCGGCCGT A G UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:114281601..114282259;chr13:114281601..114282110;chr13:114281601..114282209 26863196 MeRIP-seq:(Medium) rs1253439763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4264588,Human_RBP_ID_18417757,Human_RBP_ID_22919884,Human_RBP_ID_26324242,Human_RBP_ID_27808076 RMVar_hsa_circ_119268,RMVar_hsa_circ_165038 62822 RMVar_ID_62822 Human_SNP_ID_546453843 m1A Human chr13 + 114281653 114281653 114281653 GCTCGGCGGAGAGTGCGGCATGCGCTCGGAAAAGGAGGGGGCCGGAGGCCTTCGGGCGGCCGTTG GCTCGGCGGAGAGTGCGGCATGCGCTCGGAAAGGGAGGGGGCCGGAGGCCTTCGGGCGGCCGTTG A G UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:114281601..114281850 26863196 MeRIP-seq:(Medium) rs1340545238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4264589,Human_RBP_ID_18417757,Human_RBP_ID_21968570,Human_RBP_ID_22919884,Human_RBP_ID_26324242,Human_RBP_ID_27808076 RMVar_hsa_circ_119268,RMVar_hsa_circ_165038 62823 RMVar_ID_62823 Human_SNP_ID_546453942 m1A Human chr13 - 114281784 114281784 114281784 AGGTTTGCCCGCACCGCCCCCGCAACCGGAGGACGAAGTTGGCGGCGTCTCAGCCTCCTGCTGCT AGGTTTGCCCGCACCGCCCCCGCAACCGGAGGGCGAAGTTGGCGGCGTCTCAGCCTCCTGCTGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:114281627..114281852 26863196 MeRIP-seq:(Medium) rs1209085685 Functional Loss SNV dbSNP153 33..33 33 - - - 62824 RMVar_ID_62824 Human_SNP_ID_546454257 m1A Human chr13 - 114282102 114282100 114282103 GCCTCACCTCAGGTCGGCGGCGAAGAACTCGAAGTAGTCGTGTGCTGGCAGCGGGCGCAGCTGCT GCCTCACCTCAGGTCGGCGGCGAAGAACTCG___TAGTCGTGTGCTGGCAGCGGGCGCAGCTGCT ACTT A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:114282001..114282125 26863410 MeRIP-seq:(Medium) rs775704311 Functional Loss DEL dbSNP153 32..34 33 - - - 62825 RMVar_ID_62825 Human_SNP_ID_546454337 m1A Human chr13 - 114282256 114282256 114282256 TTTGACGGAACGGACACGTTTTACTGAAATGTATTTATTCAAAAAGCTCACACGACTCCCATATA TTTGACGGAACGGACACGTTTTACTGAAATGTGTTTATTCAAAAAGCTCACACGACTCCCATATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:114282208..114282925 26863196 MeRIP-seq:(Medium) rs1170924767 Functional Loss SNV dbSNP153 33..33 33 - - - 62826 RMVar_ID_62826 Human_SNP_ID_546455920 m1A Human chr13 + 114287484 114287484 114287484 ATGGTGGTGCGTGCCTATAGTTCCAGCTACTGAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA ATGGTGGTGCGTGCCTATAGTTCCAGCTACTGGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:114287470..114287578 32194978 MeRIP-seq:(Medium) rs1158890507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 62827 RMVar_ID_62827 Human_SNP_ID_546456222 m1A Human chr13 + 114288431 114288431 114288431 GGTCAGGAGATGAGCTGAGCCTGGCCGTGCTGAGCAGTGGAGGAAGGAAGCGCCAGGGGCAGGGC GGTCAGGAGATGAGCTGAGCCTGGCCGTGCTGCGCAGTGGAGGAAGGAAGCGCCAGGGGCAGGGC A C UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:114288385..114288522 26863196 MeRIP-seq:(Medium) rs1209156816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6260521,Human_RBP_ID_12107560 RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 62828 RMVar_ID_62828 Human_SNP_ID_546456317 m1A Human chr13 - 114288701 114288701 114288701 TCCCACACCCTATCCGTCTGTCGGTCCTGTCCAGCCCACCTCCAAAACACACGCTCATCTCTTGG TCCCACACCCTATCCGTCTGTCGGTCCTGTCCGGCCCACCTCCAAAACACACGCTCATCTCTTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:114288276..114288866 26863196 MeRIP-seq:(Medium) rs992736699 Functional Loss SNV dbSNP153 33..33 33 - - - 62829 RMVar_ID_62829 Human_SNP_ID_546459927 m1A Human chr13 + 114298969 114298969 114298969 GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCATGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCGTGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG A G UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114298926..114299025 26863196 MeRIP-seq:(Medium) rs3993409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22919914,Human_RBP_ID_24543580,Human_RBP_ID_26324248 Human_Splice_Rec_1486767,Human_Splice_Rec_1486785,Human_Splice_Rec_1486825,Human_Splice_Rec_1486839,Human_Splice_Rec_1486859 62830 RMVar_ID_62830 Human_SNP_ID_546459928 m1A Human chr13 + 114298969 114298969 114298969 GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCATGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCTTGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG A T UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114298926..114299025 26863196 MeRIP-seq:(Medium) rs3993409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22919914,Human_RBP_ID_24543580,Human_RBP_ID_26324248 Human_Splice_Rec_1486767,Human_Splice_Rec_1486785,Human_Splice_Rec_1486825,Human_Splice_Rec_1486839,Human_Splice_Rec_1486859 62831 RMVar_ID_62831 Human_SNP_ID_546461497 m1A Human chr13 + 114304852 114304852 114304852 GAGCTCGCTTCCGAGCGCGAGAGTGTGGCGGAAACAGGAGGATCTGCAAGGCAGAAGGTTCGGGG GAGCTCGCTTCCGAGCGCGAGAGTGTGGCGGATACAGGAGGATCTGCAAGGCAGAAGGTTCGGGG A T UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114304801..114304875 26863196 MeRIP-seq:(Medium) rs746478058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879665,Human_RBP_ID_26324252 Human_Splice_Rec_1486770,Human_Splice_Rec_1486788,Human_Splice_Rec_1486816,Human_Splice_Rec_1486862 62832 RMVar_ID_62832 Human_SNP_ID_546466914 m1A Human chr13 + 114324631 114324631 114324631 TCCCCAGAACCTTGGGGACCATCCCCAGCTGCATCTCCAGAATCTCGGAAGTCAGCCCGGACTAC TCCCCAGAACCTTGGGGACCATCCCCAGCTGCGTCTCCAGAATCTCGGAAGTCAGCCCGGACTAC A G CHAMP1 Ensembl:ENSG00000198824 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:114324582..114324688 26863196 MeRIP-seq:(Medium) rs782255585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4264661,Human_RBP_ID_17244073,Human_RBP_ID_17360782,Human_RBP_ID_18637296 Human_miRNA_ID_1546302 RMVar_hsa_circ_165039 62833 RMVar_ID_62833 Human_SNP_ID_260685844 m1A Human chr5 + 168291822 168291795 168291822 CGGCGTGGAGGGCGCAGCGCGCCGCGCGGCGGAGGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG CGGCGT___________________________GGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG TGGAGGGCGCAGCGCGCCGCGCGGCGGA T WWC1 Ensembl:ENSG00000113645 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:168291746..168291869 26863410 MeRIP-seq:(Medium) rs1313409879 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_8213269,Human_RBP_ID_8236999,Human_RBP_ID_19015287 62834 RMVar_ID_62834 Human_SNP_ID_260685855 m1A Human chr5 + 168291822 168291822 168291822 CGGCGTGGAGGGCGCAGCGCGCCGCGCGGCGGAGGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG CGGCGTGGAGGGCGCAGCGCGCCGCGCGGCGGCGGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG A C WWC1 Ensembl:ENSG00000113645 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:168291746..168291869 26863410 MeRIP-seq:(Medium) rs1445153769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213269,Human_RBP_ID_8236999,Human_RBP_ID_19015287 62835 RMVar_ID_62835 Human_SNP_ID_260685856 m1A Human chr5 + 168291822 168291822 168291822 CGGCGTGGAGGGCGCAGCGCGCCGCGCGGCGGAGGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG CGGCGTGGAGGGCGCAGCGCGCCGCGCGGCGGGGGAGGGCAGACGGCGGCGGCGGCGGCGCTCGG A G WWC1 Ensembl:ENSG00000113645 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:168291746..168291869 26863410 MeRIP-seq:(Medium) rs1445153769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213269,Human_RBP_ID_8236999,Human_RBP_ID_19015287 62836 RMVar_ID_62836 Human_SNP_ID_260701537 m1A Human chr5 - 168355804 168355804 168355804 CTCAGTTTTTCTACCTACACTCCTTCCTGTTCACTCCCTTACCCACCCCCATAATAAAAACAACA CTCAGTTTTTCTACCTACACTCCTTCCTGTTCGCTCCCTTACCCACCCCCATAATAAAAACAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:168355799..168355952;chr5:168355796..168355972 26863196 MeRIP-seq:(Medium) rs1372835032 Functional Loss SNV dbSNP153 33..33 33 - - - 62837 RMVar_ID_62837 Human_SNP_ID_260712998 m1A Human chr5 + 168400941 168400941 168400941 AAAGGAAAGGAAAAAGAACGAGAGAGAAAGAGAAAAAGCCCTCCAGTCTGGGTGACAAAGTGACA AAAGGAAAGGAAAAAGAACGAGAGAGAAAGAGGAAAAGCCCTCCAGTCTGGGTGACAAAGTGACA A G WWC1 Ensembl:ENSG00000113645 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:168400920..168401059 26863196 MeRIP-seq:(Medium) rs192441009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34469,RMVar_hsa_circ_313937,RMVar_hsa_circ_368423,RMVar_hsa_circ_6673,RMVar_hsa_circ_235996,RMVar_hsa_circ_45853,RMVar_hsa_circ_284868 62838 RMVar_ID_62838 Human_SNP_ID_260719238 m1A Human chr5 - 168423820 168423820 168423820 TCATGGACTTTGGGGTGCCAGACAGGGAACGCAGAGCCTGCAGGCGGCCACCTCCCTCTGCCTTC TCATGGACTTTGGGGTGCCAGACAGGGAACGCCGAGCCTGCAGGCGGCCACCTCCCTCTGCCTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:168423770..168423878 26863196 MeRIP-seq:(Medium) rs1279932312 Functional Loss SNV dbSNP153 33..33 33 - - - 62839 RMVar_ID_62839 Human_SNP_ID_260724635 m1A Human chr5 - 168444584 168444584 168444584 GCTCCTGGGGCCCAAGGGCGGGCTCACTCACCAGCTGTCTTCCAGTGTCTGTGTGCTGCTCCTGC GCTCCTGGGGCCCAAGGGCGGGCTCACTCACCTGCTGTCTTCCAGTGTCTGTGTGCTGCTCCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:168444501..168444634;chr5:168444501..168454140 26863196 MeRIP-seq:(Medium) rs1164394649 Functional Loss SNV dbSNP153 33..33 33 - - - 62840 RMVar_ID_62840 Human_SNP_ID_260727106 m1A Human chr5 - 168453913 168453913 168453913 TTACCCACCCAGAAGCCGCTCTGCCTCTGTTCACCTGCCTTTAATACACCCAAGGTAGGGCTTCC TTACCCACCCAGAAGCCGCTCTGCCTCTGTTCTCCTGCCTTTAATACACCCAAGGTAGGGCTTCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168453909..168453981 26863196 MeRIP-seq:(Medium) rs1188394794 Functional Loss SNV dbSNP153 33..33 33 - - - 62841 RMVar_ID_62841 Human_SNP_ID_260735563 m1A Human chr5 - 168486533 168486533 168486533 CGCCGGTCTCCTGCGTCCAAACCTGCTGCAGCAGCCGCGCGGAGCACTCAGACACCAGTACGTCC CGCCGGTCTCCTGCGTCCAAACCTGCTGCAGCTGCCGCGCGGAGCACTCAGACACCAGTACGTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:168486476..168486689 26863196 MeRIP-seq:(Medium) rs952079636 Functional Loss SNV dbSNP153 33..33 33 - - - 62842 RMVar_ID_62842 Human_SNP_ID_260736192 m1A Human chr5 + 168488609 168488609 168488609 GAAAAAAGTGCTTTTTTTCCCACAGGAAGAAGAGATTAAATCTCTGACTGCTGAAATTGACCGGT GAAAAAAGTGCTTTTTTTCCCACAGGAAGAAGCGATTAAATCTCTGACTGCTGAAATTGACCGGT A C RARS1 Ensembl:ENSG00000113643 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168488601..168488675 26863196 MeRIP-seq:(Medium) rs1354675753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17196653,Human_RBP_ID_22553386,Human_RBP_ID_24094792,Human_RBP_ID_27077487 Human_Splice_Rec_718578,Human_Splice_Rec_718588,Human_Splice_Rec_718616,Human_Splice_Rec_718626,Human_Splice_Rec_718634 Human_miRNA_ID_2232353,Human_miRNA_ID_2232354,Human_miRNA_ID_2232355 RMVar_hsa_circ_124053,RMVar_hsa_circ_289746,RMVar_hsa_circ_307071,RMVar_hsa_circ_375825,RMVar_hsa_circ_333202,RMVar_hsa_circ_305517,RMVar_hsa_circ_270901,RMVar_hsa_circ_276764,RMVar_hsa_circ_270821,RMVar_hsa_circ_236008,RMVar_hsa_circ_236010,RMVar_hsa_circ_236012,RMVar_hsa_circ_122411,RMVar_hsa_circ_236013,RMVar_hsa_circ_236011,RMVar_hsa_circ_236009,RMVar_hsa_circ_236006,RMVar_hsa_circ_236007,RMVar_hsa_circ_236014,RMVar_hsa_circ_236005 62843 RMVar_ID_62843 Human_SNP_ID_260737603 m1A Human chr5 + 168494384 168494384 168494384 GGTTTCAGGAGAGTGGTGAAGGCTTGAAGTAGACGGTGAGACAGGAGCTTACAAGACAGCTTAAG GGTTTCAGGAGAGTGGTGAAGGCTTGAAGTAGGCGGTGAGACAGGAGCTTACAAGACAGCTTAAG A G RARS1 Ensembl:ENSG00000113643 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13182927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1649540,Human_RBP_ID_7413053,Human_RBP_ID_15369560 RMVar_hsa_circ_29880,RMVar_hsa_circ_124053,RMVar_hsa_circ_289746,RMVar_hsa_circ_307071,RMVar_hsa_circ_333202,RMVar_hsa_circ_305517,RMVar_hsa_circ_270901,RMVar_hsa_circ_270821,RMVar_hsa_circ_236008,RMVar_hsa_circ_236010,RMVar_hsa_circ_236012,RMVar_hsa_circ_236013,RMVar_hsa_circ_236011,RMVar_hsa_circ_236009,RMVar_hsa_circ_236014,RMVar_hsa_circ_330181,RMVar_hsa_circ_336024,RMVar_hsa_circ_293764,RMVar_hsa_circ_349010,RMVar_hsa_circ_236015,RMVar_hsa_circ_236016,RMVar_hsa_circ_351023,RMVar_hsa_circ_319080,RMVar_hsa_circ_320336,RMVar_hsa_circ_314446,RMVar_hsa_circ_274915,RMVar_hsa_circ_275213,RMVar_hsa_circ_272045,RMVar_hsa_circ_236019,RMVar_hsa_circ_236021,RMVar_hsa_circ_236023,RMVar_hsa_circ_236024,RMVar_hsa_circ_236022,RMVar_hsa_circ_236020 62844 RMVar_ID_62844 Human_SNP_ID_260755658 m1A Human chr5 - 168563969 168563969 168563969 GCTCTTGAAATGGCATCCAAAGGTGATAGCACACAAGCTGACAAGCTGGTCCGTGATATTTATGG GCTCTTGAAATGGCATCCAAAGGTGATAGCACCCAAGCTGACAAGCTGGTCCGTGATATTTATGG T G PANK3 Ensembl:ENSG00000120137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168563892..168563993 26863196 MeRIP-seq:(Medium) rs747484040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4821643,Human_RBP_ID_8609380,Human_RBP_ID_15370869,Human_RBP_ID_24095136,Human_RBP_ID_27738134 Human_Splice_Rec_718684,Human_Splice_Rec_718685 RMVar_hsa_circ_116149,RMVar_hsa_circ_236052,RMVar_hsa_circ_236053,RMVar_hsa_circ_236051,RMVar_hsa_circ_278568,RMVar_hsa_circ_287370,RMVar_hsa_circ_270730,RMVar_hsa_circ_236054,RMVar_hsa_circ_236056,RMVar_hsa_circ_236057,RMVar_hsa_circ_236055,RMVar_hsa_circ_236060,RMVar_hsa_circ_378497,RMVar_hsa_circ_278821,RMVar_hsa_circ_1878,RMVar_hsa_circ_317329 62845 RMVar_ID_62845 Human_SNP_ID_260760056 m1A Human chr5 + 168579352 168579352 168579352 CGGGGCACTGAGAGCAGAGGCGGCGACTCCGGAGGTGGCTGGGCCGCGCGGCGAGGCCCGGCCGG CGGGGCACTGAGAGCAGAGGCGGCGACTCCGGGGGTGGCTGGGCCGCGCGGCGAGGCCCGGCCGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:168579301..168579557 26863196 MeRIP-seq:(Medium) rs778282411 Functional Loss SNV dbSNP153 33..33 33 - - - 62846 RMVar_ID_62846 Human_SNP_ID_260760060 m1A Human chr5 - 168579359 168579359 168579359 GGAGGAACCGGCCGGGCCTCGCCGCGCGGCCCAGCCACCTCCGGAGTCGCCGCCTCTGCTCTCAG GGAGGAACCGGCCGGGCCTCGCCGCGCGGCCCGGCCACCTCCGGAGTCGCCGCCTCTGCTCTCAG T C PANK3 Ensembl:ENSG00000120137 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168579251..168579550 26863196 MeRIP-seq:(Medium) rs1013793161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_637271,Human_RBP_ID_4845476,Human_RBP_ID_9335448,Human_RBP_ID_18837838 RMVar_hsa_circ_116149,RMVar_hsa_circ_236054 62847 RMVar_ID_62847 Human_SNP_ID_260760109 m1A Human chr5 - 168579501 168579501 168579501 GCCCCGGAGCGGCGAGGCCGGCGGCCTTCCCCAGCTTGCTCGGTCCCGGCCACCCCTCGCGGGGG GCCCCGGAGCGGCGAGGCCGGCGGCCTTCCCCGGCTTGCTCGGTCCCGGCCACCCCTCGCGGGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:168579401..168579600 26863410 MeRIP-seq:(Medium) rs1271591517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250031,Human_RBP_ID_637272,Human_RBP_ID_840119,Human_RBP_ID_4845477,Human_RBP_ID_5242322,Human_RBP_ID_5449574,Human_RBP_ID_5476445,Human_RBP_ID_5509215,Human_RBP_ID_18044139,Human_RBP_ID_18465266,Human_RBP_ID_26792205 Human_miRNA_ID_2683631 RMVar_hsa_circ_116149,RMVar_hsa_circ_236054 62848 RMVar_ID_62848 Human_SNP_ID_260768611 m1A Human chr5 + 168616439 168616439 168616439 AGTCTCGCTTCTGCCGAGGTGTCCCTGATGCCAAGATTCGCATTTTTGACCTGGGGCGGAAAAAG AGTCTCGCTTCTGCCGAGGTGTCCCTGATGCCCAGATTCGCATTTTTGACCTGGGGCGGAAAAAG A C RPL10P9 Ensembl:ENSG00000233913 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs896476430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17416325 62849 RMVar_ID_62849 Human_SNP_ID_261010478 m1A Human chr5 - 169583827 169583827 169583827 AGCGGCTCCTAATGGGAGCTCAGGGCGTCCACATTGAGGACGCTAACTCCACAGTCGCCGGCCCA AGCGGCTCCTAATGGGAGCTCAGGGCGTCCACCTTGAGGACGCTAACTCCACAGTCGCCGGCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:169583776..169583946;chr5:169583776..169584015 26863196 MeRIP-seq:(Medium) rs904572038 Functional Loss SNV dbSNP153 33..33 33 - - - 62850 RMVar_ID_62850 Human_SNP_ID_261010485 m1A Human chr5 - 169583838 169583838 169583838 CTGCCGCAGCCAGCGGCTCCTAATGGGAGCTCAGGGCGTCCACATTGAGGACGCTAACTCCACAG CTGCCGCAGCCAGCGGCTCCTAATGGGAGCTCTGGGCGTCCACATTGAGGACGCTAACTCCACAG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:169583788..169583892 26863196 MeRIP-seq:(Medium) rs892083101 Functional Loss SNV dbSNP153 33..33 33 - - - 62851 RMVar_ID_62851 Human_SNP_ID_261010487 m1A Human chr5 - 169583849 169583849 169583849 CTAGTCCCCTGCTGCCGCAGCCAGCGGCTCCTAATGGGAGCTCAGGGCGTCCACATTGAGGACGC CTAGTCCCCTGCTGCCGCAGCCAGCGGCTCCTGATGGGAGCTCAGGGCGTCCACATTGAGGACGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:169583800..169583938 26863196 MeRIP-seq:(Medium) rs555675528 Functional Loss SNV dbSNP153 33..33 33 - - - 62852 RMVar_ID_62852 Human_SNP_ID_261012985 m1A Human chr5 + 169593373 169593373 169593373 TTTTTGGCTTTAGATAGAAAAACTGAAAGTGGAATTAGATGAAGCCAGGCTTAGTGAAAAGCAGC TTTTTGGCTTTAGATAGAAAAACTGAAAGTGGGATTAGATGAAGCCAGGCTTAGTGAAAAGCAGC A G SPDL1 Ensembl:ENSG00000040275 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:169591125..169593404 32194978 MeRIP-seq:(Medium) rs779929376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1991876,Human_RBP_ID_3764609,Human_RBP_ID_15371987,Human_RBP_ID_24095487,Human_RBP_ID_26351722 Human_Splice_Rec_719070,Human_Splice_Rec_719094,Human_Splice_Rec_719108,Human_Splice_Rec_719116,Human_Splice_Rec_719140,Human_Splice_Rec_719160,Human_Splice_Rec_719166,Human_Splice_Rec_719174,Human_Splice_Rec_719176 RMVar_hsa_circ_60737,RMVar_hsa_circ_54390,RMVar_hsa_circ_73615,RMVar_hsa_circ_317736,RMVar_hsa_circ_236101,RMVar_hsa_circ_305158,RMVar_hsa_circ_29723,RMVar_hsa_circ_236102 62853 RMVar_ID_62853 Human_SNP_ID_261013376 m1A Human chr5 - 169594600 169594592 169594601 GACTGATACTTGACTTTCATACTGATGAGCTGACGTTCCATTGCTGCCCTTCGATCTTCCACCTA GACTGATACTTGACTTTCATACTGATGAGCT_________TTGCTGCCCTTCGATCTTCCACCTA ATGGAACGTC A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:169594446..169594675 32194978 MeRIP-seq:(Medium) rs762557206 Functional Loss DEL dbSNP153 32..40 33 - - - 62854 RMVar_ID_62854 Human_SNP_ID_261084323 m1A Human chr5 + 169883343 169883343 169883343 CTCTAAGGACCTCCAAGTTCCTGCTTCCAAGCATATGCTAACAGGACCATTGCTTTGCACCTTGG CTCTAAGGACCTCCAAGTTCCTGCTTCCAAGCGTATGCTAACAGGACCATTGCTTTGCACCTTGG A G DOCK2 Ensembl:ENSG00000134516 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:169883280..169883431 32194978 MeRIP-seq:(Medium) rs1312134315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236106,RMVar_hsa_circ_107698,RMVar_hsa_circ_99424,RMVar_hsa_circ_236115,RMVar_hsa_circ_82482,RMVar_hsa_circ_87451,RMVar_hsa_circ_98887,RMVar_hsa_circ_236121,RMVar_hsa_circ_119252,RMVar_hsa_circ_95210,RMVar_hsa_circ_236124,RMVar_hsa_circ_76782,RMVar_hsa_circ_236126,RMVar_hsa_circ_236125,RMVar_hsa_circ_236122,RMVar_hsa_circ_236123 62855 RMVar_ID_62855 Human_SNP_ID_261267716 m1A Human chr5 + 170633736 170633731 170633736 GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GCGAGGGGGCGGGGGGGCGGAGGGGGGG_____GGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GACGGA G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:170633701..170633775;chr5:170633615..170633775 26863196 MeRIP-seq:(Medium) rs1266920254 Functional Loss DEL dbSNP153 29..33 33 - - - 62856 RMVar_ID_62856 Human_SNP_ID_261267724 m1A Human chr5 + 170633736 170633734 170633736 GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GCGAGGGGGCGGGGGGGCGGAGGGGGGGACG__GGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GGA G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:170633701..170633775;chr5:170633615..170633775 26863196 MeRIP-seq:(Medium) rs1491162474 Functional Loss DEL dbSNP153 32..33 33 - - - 62857 RMVar_ID_62857 Human_SNP_ID_261267725 m1A Human chr5 + 170633736 170633735 170633736 GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGG_GGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GA G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:170633701..170633775;chr5:170633615..170633775 26863196 MeRIP-seq:(Medium) rs1283107123 Functional Loss DEL dbSNP153 33..33 33 - - - 62858 RMVar_ID_62858 Human_SNP_ID_261267727 m1A Human chr5 + 170633736 170633736 170633736 GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT GCGAGGGGGCGGGGGGGCGGAGGGGGGGACGGGGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGAT A G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:170633701..170633775;chr5:170633615..170633775 26863196 MeRIP-seq:(Medium) rs1474686870 Functional Loss SNV dbSNP153 33..33 33 - - - 62859 RMVar_ID_62859 Human_SNP_ID_261267750 m1A Human chr5 + 170633760 170633752 170633760 GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG GGGGACGGAGGGGGGGGCGGGGGGC________GGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG CGGGGCGGA C KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:170633689..170633766 26863196 MeRIP-seq:(Medium) rs1333969268 Functional Loss DEL dbSNP153 26..33 33 - - - 62860 RMVar_ID_62860 Human_SNP_ID_261267754 m1A Human chr5 + 170633760 170633756 170633760 GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG GGGGACGGAGGGGGGGGCGGGGGGCGGGG____GGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG GCGGA G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:170633689..170633766 26863196 MeRIP-seq:(Medium) rs1393880963 Functional Loss DEL dbSNP153 30..33 33 - - - 62861 RMVar_ID_62861 Human_SNP_ID_261267760 m1A Human chr5 + 170633760 170633760 170633760 GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGGGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG A G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:170633689..170633766 26863196 MeRIP-seq:(Medium) rs1376071099 Functional Loss SNV dbSNP153 33..33 33 - - - 62862 RMVar_ID_62862 Human_SNP_ID_261325064 m1A Human chr5 + 170862627 170862627 170862627 GCTGCGTCTGGGGGGAGTTGCGAGGGAGGGCTACGCGGCCGCCTCTTCGGAGGAGGAAACCCGGG GCTGCGTCTGGGGGGAGTTGCGAGGGAGGGCTGCGCGGCCGCCTCTTCGGAGGAGGAAACCCGGG A G RANBP17 Ensembl:ENSG00000204764 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:170862591..170862747 26863196 MeRIP-seq:(Medium) rs1431328889 Functional Loss SNV dbSNP153 33..33 33 - - - 62863 RMVar_ID_62863 Human_SNP_ID_261359876 m1A Human chr5 - 171002825 171002825 171002825 CCATGACTGTATCTCTGATACACCTGACATTCACTCCATTTCCCCATATTTCCTTCTTTCCTGTT CCATGACTGTATCTCTGATACACCTGACATTCCCTCCATTTCCCCATATTTCCTTCTTTCCTGTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:171002775..171003095 26863196 MeRIP-seq:(Medium) rs909624779 Functional Loss SNV dbSNP153 33..33 33 - - - 62864 RMVar_ID_62864 Human_SNP_ID_261359923 m1A Human chr5 - 171002957 171002956 171002957 GACACATATACTTTCTGCTCCCTGGCTCCTTCAGTTGTACTCACTCTTTGTTGAGTCTCCCACAG GACACATATACTTTCTGCTCCCTGGCTCCTTC_GTTGTACTCACTCTTTGTTGAGTCTCCCACAG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:171002765..171003166 26863196 MeRIP-seq:(Medium) rs756111053 Functional Loss DEL dbSNP153 33..33 33 - - - 62865 RMVar_ID_62865 Human_SNP_ID_261361225 m1A Human chr5 + 171007335 171007331 171007335 TTGTCGGGCAGTGGGGGAGAGCTAGTTGCAGAAAGAAACTGTAAACCAGACCAGGTGTGGAGAGG TTGTCGGGCAGTGGGGGAGAGCTAGTTGC____AGAAACTGTAAACCAGACCAGGTGTGGAGAGG CAGAA C RANBP17 Ensembl:ENSG00000204764 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:171007306..171007543 26863196 MeRIP-seq:(Medium) rs1304358440 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_70189,RMVar_hsa_circ_123008,RMVar_hsa_circ_302008,RMVar_hsa_circ_78009,RMVar_hsa_circ_105629,RMVar_hsa_circ_236145,RMVar_hsa_circ_236146,RMVar_hsa_circ_236144,RMVar_hsa_circ_321595,RMVar_hsa_circ_126900,RMVar_hsa_circ_46729,RMVar_hsa_circ_2584,RMVar_hsa_circ_13245,RMVar_hsa_circ_236155,RMVar_hsa_circ_329744,RMVar_hsa_circ_120893,RMVar_hsa_circ_236163,RMVar_hsa_circ_236167,RMVar_hsa_circ_82725,RMVar_hsa_circ_377754,RMVar_hsa_circ_19438,RMVar_hsa_circ_21021,RMVar_hsa_circ_15450,RMVar_hsa_circ_27311,RMVar_hsa_circ_40886,RMVar_hsa_circ_2618,RMVar_hsa_circ_47913,RMVar_hsa_circ_38919,RMVar_hsa_circ_289351,RMVar_hsa_circ_320404,RMVar_hsa_circ_292738,RMVar_hsa_circ_78739,RMVar_hsa_circ_41610,RMVar_hsa_circ_37928,RMVar_hsa_circ_51723,RMVar_hsa_circ_236170,RMVar_hsa_circ_236171,RMVar_hsa_circ_376819,RMVar_hsa_circ_33776,RMVar_hsa_circ_24887,RMVar_hsa_circ_340256,RMVar_hsa_circ_236173,RMVar_hsa_circ_20521 62866 RMVar_ID_62866 Human_SNP_ID_261435231 m1A Human chr5 - 171309297 171309297 171309297 GGAGGCGGCTGGGTCCCCGTTACGGCGCGGCCATGGAGCGCCCGGCGCCTCTCGTCGCACTGAAA GGAGGCGGCTGGGTCCCCGTTACGGCGCGGCCGTGGAGCGCCCGGCGCCTCTCGTCGCACTGAAA T C AC091980.2 Ensembl:ENSG00000275038 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:171309249..171309500;chr5:171309249..171309476 26863196 MeRIP-seq:(Medium) rs1026893431 Functional Loss SNV dbSNP153 33..33 33 - - - 62867 RMVar_ID_62867 Human_SNP_ID_261435783 m1A Human chr5 + 171310518 171310518 171310518 CCACTACCCCCGCCCCCCTCTGCCTCCCCCAAACACACCCCCACCCCGCCTTCGCAGATTGTACC CCACTACCCCCGCCCCCCTCTGCCTCCCCCAACCACACCCCCACCCCGCCTTCGCAGATTGTACC A C TLX3 Ensembl:ENSG00000164438 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:171310515..171310608 26863196 MeRIP-seq:(Medium) rs1190746493 Functional Loss SNV dbSNP153 33..33 33 - - - 62868 RMVar_ID_62868 Human_SNP_ID_261456416 m1A Human chr5 - 171387900 171387900 171387900 CTTAGGTAGGAGAGAAGGCGGACGGAGATAAAAGAACGCTGCTCCAGAGAACAACCGCGCAGGAC CTTAGGTAGGAGAGAAGGCGGACGGAGATAAAGGAACGCTGCTCCAGAGAACAACCGCGCAGGAC T C RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:171387851..171387950 32194978 MeRIP-seq:(Medium) rs11551555 Functional Loss SNV dbSNP153 33..33 33 - - - 62869 RMVar_ID_62869 Human_SNP_ID_261456417 m1A Human chr5 - 171387901 171387901 171387901 ACTTAGGTAGGAGAGAAGGCGGACGGAGATAAAAGAACGCTGCTCCAGAGAACAACCGCGCAGGA ACTTAGGTAGGAGAGAAGGCGGACGGAGATAAGAGAACGCTGCTCCAGAGAACAACCGCGCAGGA T C RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:171387851..171388229;chr5:171387690..171387950;chr5:171387701..171390100;chr5:171387725..171390100 26863196 MeRIP-seq:(Medium) rs11551547 Functional Loss SNV dbSNP153 33..33 33 - - - 62870 RMVar_ID_62870 Human_SNP_ID_261456418 m1A Human chr5 + 171387904 171387904 171387904 TGCGCGGTTGTTCTCTGGAGCAGCGTTCTTTTATCTCCGTCCGCCTTCTCTCCTACCTAAGTGCG TGCGCGGTTGTTCTCTGGAGCAGCGTTCTTTTGTCTCCGTCCGCCTTCTCTCCTACCTAAGTGCG A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr5:171387851..171387925;chr5:171387851..171387950 26863196 MeRIP-seq:(Medium) rs757830185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165912,Human_RBP_ID_637397,Human_RBP_ID_788433,Human_RBP_ID_946322,Human_RBP_ID_1211793,Human_RBP_ID_1390931,Human_RBP_ID_1650016,Human_RBP_ID_1992144,Human_RBP_ID_2915887,Human_RBP_ID_3765007,Human_RBP_ID_4846151,Human_RBP_ID_5427084,Human_RBP_ID_5449595,Human_RBP_ID_5476460,Human_RBP_ID_5509235,Human_RBP_ID_7415150,Human_RBP_ID_8133752,Human_RBP_ID_8609723,Human_RBP_ID_8887983,Human_RBP_ID_9398646,Human_RBP_ID_17299354,Human_RBP_ID_17412844,Human_RBP_ID_17528947,Human_RBP_ID_18044331,Human_RBP_ID_18202132,Human_RBP_ID_18210484,Human_RBP_ID_18448498,Human_RBP_ID_18838079,Human_RBP_ID_22100552,Human_RBP_ID_22298112,Human_RBP_ID_22511961,Human_RBP_ID_23214368,Human_RBP_ID_24095929,Human_RBP_ID_27077725,Human_RBP_ID_27160418,Human_RBP_ID_27334021,Human_RBP_ID_27513635 Human_miRNA_ID_2134889,Human_miRNA_ID_2664837,Human_miRNA_ID_2913619 RMVar_hsa_circ_236196,RMVar_hsa_circ_78173,RMVar_hsa_circ_95416,RMVar_hsa_circ_80317,RMVar_hsa_circ_236198,RMVar_hsa_circ_76390,RMVar_hsa_circ_236199,RMVar_hsa_circ_236197 62871 RMVar_ID_62871 Human_SNP_ID_261457240 m1A Human chr5 - 171390106 171390106 171390106 TTAAGTACCGTTCTTAAAGATAACTGGTGCTCATTTTCATCATTATCCACCTTAAAGTGATAATC TTAAGTACCGTTCTTAAAGATAACTGGTGCTCCTTTTCATCATTATCCACCTTAAAGTGATAATC T G RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:171390038..171390182 26863196 MeRIP-seq:(Medium) rs1324989400 Functional Loss SNV dbSNP153 33..33 33 - - - 62872 RMVar_ID_62872 Human_SNP_ID_261457651 m1A Human chr5 - 171391343 171391343 171391343 CTGCCTTCGTAATTCATTGCCTCTGCTTCAACAATGTGCAACTCATCCTTTGCACCAGCCCCTAA CTGCCTTCGTAATTCATTGCCTCTGCTTCAACGATGTGCAACTCATCCTTTGCACCAGCCCCTAA T C RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr5:171391275..171391342;chr5:171391301..171391425 26863196,32194978 MeRIP-seq:(Medium) rs142102985 Functional Loss SNV dbSNP153 33..33 33 - - - 62873 RMVar_ID_62873 Human_SNP_ID_261457652 m1A Human chr5 - 171391343 171391343 171391343 CTGCCTTCGTAATTCATTGCCTCTGCTTCAACAATGTGCAACTCATCCTTTGCACCAGCCCCTAA CTGCCTTCGTAATTCATTGCCTCTGCTTCAACCATGTGCAACTCATCCTTTGCACCAGCCCCTAA T G RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr5:171391275..171391342;chr5:171391301..171391425 26863196,32194978 MeRIP-seq:(Medium) rs142102985 Functional Loss SNV dbSNP153 33..33 33 - - - 62874 RMVar_ID_62874 Human_SNP_ID_261458243 m1A Human chr5 - 171392980 171392977 171392981 CGGAAGTATATCAAGTTTCTAAAATCATACTTACTCTTCATCATCATCCTCTTCATCATCATCGT CGGAAGTATATCAAGTTTCTAAAATCATACT____CTTCATCATCATCCTCTTCATCATCATCGT GAGTA G RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr5:171392785..171393029;chr5:171392805..171393023 26863410 MeRIP-seq:(Medium) rs750620267 Functional Loss DEL dbSNP153 32..35 33 - - - 62875 RMVar_ID_62875 Human_SNP_ID_261462545 m1A Human chr5 + 171405306 171405306 171405306 ACCTTTTGGAAATTCATTTCTTTTTCAGGGACAAGAATCCTTCAAGAAACAGGAAAAAACTCCTA ACCTTTTGGAAATTCATTTCTTTTTCAGGGACGAGAATCCTTCAAGAAACAGGAAAAAACTCCTA A G NPM1 Ensembl:ENSG00000181163 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:171405301..171405375 32194978 MeRIP-seq:(Medium) rs758630739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76899,Human_RBP_ID_637408,Human_RBP_ID_945512,Human_RBP_ID_1650094,Human_RBP_ID_1992209,Human_RBP_ID_2916075,Human_RBP_ID_4852609,Human_RBP_ID_8267450,Human_RBP_ID_9398666,Human_RBP_ID_15375817,Human_RBP_ID_18537871,Human_RBP_ID_18838107,Human_RBP_ID_23051428,Human_RBP_ID_24548155,Human_RBP_ID_25878861,Human_RBP_ID_26351756,Human_RBP_ID_27077801,Human_RBP_ID_27827097 Human_Splice_Rec_720640,Human_Splice_Rec_720641,Human_Splice_Rec_720660,Human_Splice_Rec_720661,Human_Splice_Rec_720688,Human_Splice_Rec_720689,Human_Splice_Rec_720708,Human_Splice_Rec_720709,Human_Splice_Rec_720730 Human_miRNA_ID_2875101,Human_miRNA_ID_2875102 RMVar_hsa_circ_236205,RMVar_hsa_circ_362239,RMVar_hsa_circ_95388,RMVar_hsa_circ_236203,RMVar_hsa_circ_369661,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_109259,RMVar_hsa_circ_236220,RMVar_hsa_circ_371814,RMVar_hsa_circ_236223,RMVar_hsa_circ_113068,RMVar_hsa_circ_367789,RMVar_hsa_circ_236222,RMVar_hsa_circ_360179,RMVar_hsa_circ_236224 62876 RMVar_ID_62876 Human_SNP_ID_261474587 m1A Human chr5 + 171450916 171450916 171450916 TTGAGTTTTCGGCTCGTTTTTCTTTCTCCCCCAGCAGGGGCCAGCGGCACCCGCCAGTGCCCGTG TTGAGTTTTCGGCTCGTTTTTCTTTCTCCCCCGGCAGGGGCCAGCGGCACCCGCCAGTGCCCGTG A G FGF18 Ensembl:ENSG00000156427 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:171450880..171450951 26863196 MeRIP-seq:(Medium) rs889843864 Functional Loss SNV dbSNP153 33..33 33 - - - 62877 RMVar_ID_62877 Human_SNP_ID_261620595 m1A Human chr5 - 172044805 172044805 172044805 CTTCTCCTTCATTCTCTGTGAACATGTAACTCAGGACCCCTTTTCCCTCTTGCGTCTGTGCCAGC CTTCTCCTTCATTCTCTGTGAACATGTAACTCCGGACCCCTTTTCCCTCTTGCGTCTGTGCCAGC T G STK10 Ensembl:ENSG00000072786 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:172044517..172045470 32194978 MeRIP-seq:(Medium) rs749346148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_637597 62878 RMVar_ID_62878 Human_SNP_ID_261626288 m1A Human chr5 + 172064542 172064542 172064542 GGAAGAGCTTACTTCCAGATGGAGGCAGGGCAATCGAGGAAGGCTGCATGGAGGAGGGGATAATG GGAAGAGCTTACTTCCAGATGGAGGCAGGGCAGTCGAGGAAGGCTGCATGGAGGAGGGGATAATG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:172064494..172064626 26863196 MeRIP-seq:(Medium) rs1330745980 Functional Loss SNV dbSNP153 33..33 33 - - - 62879 RMVar_ID_62879 Human_SNP_ID_261635621 m1A Human chr5 - 172098882 172098882 172098882 TGGTGATGGTGGTGGTGATGGTGGTGAAGGTGATGATGGTGGTGGTGGTGATGATGATGATGATG TGGTGATGGTGGTGGTGATGGTGGTGAAGGTGTTGATGGTGGTGGTGGTGATGATGATGATGATG T A STK10 Ensembl:ENSG00000072786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:172098860..172099206;chr5:172098839..172099266 26863196 MeRIP-seq:(Medium) rs910691661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82281,RMVar_hsa_circ_236246,RMVar_hsa_circ_89822,RMVar_hsa_circ_236247,RMVar_hsa_circ_49873,RMVar_hsa_circ_55124,RMVar_hsa_circ_236250,RMVar_hsa_circ_125608,RMVar_hsa_circ_268979 62880 RMVar_ID_62880 Human_SNP_ID_261635622 m1A Human chr5 - 172098882 172098882 172098882 TGGTGATGGTGGTGGTGATGGTGGTGAAGGTGATGATGGTGGTGGTGGTGATGATGATGATGATG TGGTGATGGTGGTGGTGATGGTGGTGAAGGTGGTGATGGTGGTGGTGGTGATGATGATGATGATG T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:172098860..172099206;chr5:172098839..172099266 26863196 MeRIP-seq:(Medium) rs910691661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82281,RMVar_hsa_circ_236246,RMVar_hsa_circ_89822,RMVar_hsa_circ_236247,RMVar_hsa_circ_49873,RMVar_hsa_circ_55124,RMVar_hsa_circ_236250,RMVar_hsa_circ_125608,RMVar_hsa_circ_268979 62881 RMVar_ID_62881 Human_SNP_ID_261637951 m1A Human chr5 - 172106735 172106735 172106735 ACGACTACAAAGCCGACATCTGGTCCCTGGGCATCACGCTGATTGAGATGGCCCAGATCGAGCCG ACGACTACAAAGCCGACATCTGGTCCCTGGGCGTCACGCTGATTGAGATGGCCCAGATCGAGCCG T C STK10 Ensembl:ENSG00000072786 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172106684..172106819 26863196 MeRIP-seq:(Medium) rs201487887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_164502,Human_RBP_ID_18838237 Human_Splice_Rec_720942,Human_Splice_Rec_720994,Human_Splice_Rec_721004,Human_Splice_Rec_721012 RMVar_hsa_circ_82281,RMVar_hsa_circ_27001,RMVar_hsa_circ_236246,RMVar_hsa_circ_89822,RMVar_hsa_circ_236247,RMVar_hsa_circ_49873,RMVar_hsa_circ_55124,RMVar_hsa_circ_236250,RMVar_hsa_circ_125608,RMVar_hsa_circ_28961,RMVar_hsa_circ_308532,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818 62882 RMVar_ID_62882 Human_SNP_ID_261658973 m1A Human chr5 - 172188042 172188042 172188042 GAGCCCGAGCCGGCGCCACCGCGCCCCCGGCCATGGCTTTTGCCAATTTCCGCCGCATCCTGCGC GAGCCCGAGCCGGCGCCACCGCGCCCCCGGCCGTGGCTTTTGCCAATTTCCGCCGCATCCTGCGC T C STK10 Ensembl:ENSG00000072786 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172187993..172188354 26863196 MeRIP-seq:(Medium) rs990782881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4822034 62883 RMVar_ID_62883 Human_SNP_ID_261681896 m1A Human chr5 + 172275600 172275600 172275600 CTTATTGCTTCACCCTTTATGAAACTCTCATGACTCAATTCTTAGTATTTTCCTCCTCTTTCACT CTTATTGCTTCACCCTTTATGAAACTCTCATGTCTCAATTCTTAGTATTTTCCTCCTCTTTCACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172275598..172275665 26863196 MeRIP-seq:(Medium) rs1020840559 Functional Loss SNV dbSNP153 33..33 33 - - - 62884 RMVar_ID_62884 Human_SNP_ID_261683999 m1A Human chr5 + 172283488 172283488 172283488 AGCGGAGCGCGGGGAATGACGTGGAAGAGGGGATGACAAAGGGGCGCGGGGGCCCGGCGCGGCCC AGCGGAGCGCGGGGAATGACGTGGAAGAGGGGGTGACAAAGGGGCGCGGGGGCCCGGCGCGGCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:172283467..172283675 26863196 MeRIP-seq:(Medium) rs1437782451 Functional Loss SNV dbSNP153 33..33 33 - - - 62885 RMVar_ID_62885 Human_SNP_ID_261684097 m1A Human chr5 - 172283729 172283729 172283729 CGGAGCTCGGCGGTGGCGCCGGAGGAGGCTGCAGCGGCGGCGGCGGCGGGCCCGGACGAGCGTCC CGGAGCTCGGCGGTGGCGCCGGAGGAGGCTGCGGCGGCGGCGGCGGCGGGCCCGGACGAGCGTCC T C UBTD2 Ensembl:ENSG00000168246 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:172283526..172283817 26863196 MeRIP-seq:(Medium) rs928897967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250900,Human_RBP_ID_1069528,Human_RBP_ID_4845482,Human_RBP_ID_8213280,Human_RBP_ID_9350065,Human_RBP_ID_18425049,Human_RBP_ID_18471956,Human_RBP_ID_23120208,Human_RBP_ID_26792211 62886 RMVar_ID_62886 Human_SNP_ID_261684099 m1A Human chr5 - 172283736 172283736 172283736 GCCTGTCCGGAGCTCGGCGGTGGCGCCGGAGGAGGCTGCAGCGGCGGCGGCGGCGGGCCCGGACG GCCTGTCCGGAGCTCGGCGGTGGCGCCGGAGGGGGCTGCAGCGGCGGCGGCGGCGGGCCCGGACG T C UBTD2 Ensembl:ENSG00000168246 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:172283576..172284100;chr5:172283620..172284040 26863196 MeRIP-seq:(Medium) rs1450270213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250900,Human_RBP_ID_1069528,Human_RBP_ID_3783444,Human_RBP_ID_4845482,Human_RBP_ID_8213280,Human_RBP_ID_9436614,Human_RBP_ID_18425049,Human_RBP_ID_18471956,Human_RBP_ID_22727751,Human_RBP_ID_23120208 62887 RMVar_ID_62887 Human_SNP_ID_261684132 m1A Human chr5 - 172283844 172283844 172283844 CCGGGGGTTGAGGTAGAAGTGGGCGCGGAGGAAGGGGCCGAGCCAAGGCGGTGGGTGGAGCGGCG CCGGGGGTTGAGGTAGAAGTGGGCGCGGAGGAGGGGGCCGAGCCAAGGCGGTGGGTGGAGCGGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172283540..172284125 26863196 MeRIP-seq:(Medium) rs1330658057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213280,Human_RBP_ID_8730250,Human_RBP_ID_9354613,Human_RBP_ID_9437160 62888 RMVar_ID_62888 Human_SNP_ID_261728304 m1A Human chr5 + 172454330 172454330 172454330 GCCGCTTCTGCACGTCTAGCACCTTCACCTCCACGATGCTGCGCCGCGGCGGCATGGCCGCTCCT GCCGCTTCTGCACGTCTAGCACCTTCACCTCCCCGATGCTGCGCCGCGGCGGCATGGCCGCTCCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:172454276..172454457 26863196 MeRIP-seq:(Medium) rs746331779 Functional Loss SNV dbSNP153 33..33 33 - - - 62889 RMVar_ID_62889 Human_SNP_ID_261728308 m1A Human chr5 - 172454337 172454337 172454337 CGGGCGGAGGAGCGGCCATGCCGCCGCGGCGCAGCATCGTGGAGGTGAAGGTGCTAGACGTGCAG CGGGCGGAGGAGCGGCCATGCCGCCGCGGCGCCGCATCGTGGAGGTGAAGGTGCTAGACGTGCAG T G SH3PXD2B Ensembl:ENSG00000174705 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:172454276..172454500 26863196 MeRIP-seq:(Medium) rs1388377692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18448507,Human_RBP_ID_19016129 Human_Splice_Rec_721033,Human_Splice_Rec_721059,Human_Splice_Rec_721091 62890 RMVar_ID_62890 Human_SNP_ID_261728379 m1A Human chr5 + 172454478 172454478 172454478 GGAGCTGAGCGCAATCGCAGCCGGGGCCGAGCACGAGCCGCCGCCGCCACCGCCGCCGCCCTTCG GGAGCTGAGCGCAATCGCAGCCGGGGCCGAGCGCGAGCCGCCGCCGCCACCGCCGCCGCCCTTCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:172454396..172454500 26863410 MeRIP-seq:(Medium) rs1287366427 Functional Loss SNV dbSNP153 33..33 33 - - - 62891 RMVar_ID_62891 Human_SNP_ID_261775023 m1A Human chr5 - 172641295 172641295 172641295 CCGGGGTCGACGCTCCGGGGCATCGCAGCTGCACGGGCGAGCCGGCGGGCGGCAGCTGGGGCGGG CCGGGGTCGACGCTCCGGGGCATCGCAGCTGCTCGGGCGAGCCGGCGGGCGGCAGCTGGGGCGGG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr5:172641251..172641420;chr5:172641246..172641391 26863196 MeRIP-seq:(Medium) rs1307810214 Functional Loss SNV dbSNP153 33..33 33 - - - 62892 RMVar_ID_62892 Human_SNP_ID_261785053 m1A Human chr5 - 172684127 172684127 172684127 CACGCGGGGCCGGGGACTCACCGAGGAGACGCAGCTGGCCCGCGACGCCGCCGCGCACGGCGAAG CACGCGGGGCCGGGGACTCACCGAGGAGACGCTGCTGGCCCGCGACGCCGCCGCGCACGGCGAAG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:172684013..172684232 26863196 MeRIP-seq:(Medium) rs1199532738 Functional Loss SNV dbSNP153 33..33 33 - - - 62893 RMVar_ID_62893 Human_SNP_ID_261785892 m1A Human chr5 + 172687339 172687339 172687339 GAGAGAGAGAATGAACGTGTAGCGATTTTACCAGGGGTCCCGGCTCCGGGAGGAGACGTGCAATC GAGAGAGAGAATGAACGTGTAGCGATTTTACCGGGGGTCCCGGCTCCGGGAGGAGACGTGCAATC A G NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:172687304..172687475 26863196 MeRIP-seq:(Medium) rs953097804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5214654,Human_RBP_ID_24096895 Human_miRNA_ID_961109 62894 RMVar_ID_62894 Human_SNP_ID_261785900 m1A Human chr5 + 172687357 172687354 172687357 GTAGCGATTTTACCAGGGGTCCCGGCTCCGGGAGGAGACGTGCAATCCGGAGCCCCGACATTGGC GTAGCGATTTTACCAGGGGTCCCGGCTCCG___GGAGACGTGCAATCCGGAGCCCCGACATTGGC GGGA G NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:172687307..172687434;chr5:172687308..172687495 26863196 MeRIP-seq:(Medium) rs1483196882 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5214654 62895 RMVar_ID_62895 Human_SNP_ID_261786517 m1A Human chr5 + 172689966 172689966 172689966 TCTCTTGTTATTCAGGGGTGTCCACAGTTAGGAAGGGACCTGGGGCCTTGTCCCACCACCTTCCT TCTCTTGTTATTCAGGGGTGTCCACAGTTAGGGAGGGACCTGGGGCCTTGTCCCACCACCTTCCT A G NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3205179 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - GWAS_ID_7685,GWAS_ID_7686 62896 RMVar_ID_62896 Human_SNP_ID_261786729 m1A Human chr5 + 172690722 172690701 172690722 TGCCTTCTTGACCAGAACCTGCTGTGCGCTTCACAGAACCTCCTCTTCATTGGAAATGCTGGGCA TGCCTTCTTGAC_____________________CAGAACCTCCTCTTCATTGGAAATGCTGGGCA CCAGAACCTGCTGTGCGCTTCA C NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172690673..172690909 26863196 MeRIP-seq:(Medium) rs531001850 Functional Loss DEL dbSNP153 13..33 33 - - - 62897 RMVar_ID_62897 Human_SNP_ID_261786738 m1A Human chr5 + 172690722 172690722 172690722 TGCCTTCTTGACCAGAACCTGCTGTGCGCTTCACAGAACCTCCTCTTCATTGGAAATGCTGGGCA TGCCTTCTTGACCAGAACCTGCTGTGCGCTTCCCAGAACCTCCTCTTCATTGGAAATGCTGGGCA A C NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172690673..172690909 26863196 MeRIP-seq:(Medium) rs1409108070 Functional Loss SNV dbSNP153 33..33 33 - - - 62898 RMVar_ID_62898 Human_SNP_ID_261806471 m1A Human chr5 + 172768800 172768800 172768800 GCTGGGAGAGGTCGTAATGGGGCTCTGAAGGTAGCTCAGCGCACTGTTCGTGGAGTGGACAGGGA GCTGGGAGAGGTCGTAATGGGGCTCTGAAGGTGGCTCAGCGCACTGTTCGTGGAGTGGACAGGGA A G AC022217.4 Ensembl:ENSG00000253736 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:172768776..172768800 26863196 MeRIP-seq:(Medium) rs1357792357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5615608 RMVar_hsa_circ_236261 62899 RMVar_ID_62899 Human_SNP_ID_261807257 m1A Human chr5 + 172771101 172771101 172771101 CGAACCAAAAGCCGCTTTTGGACTGAGAGAGGAGCGTCACGCGGGGCTCCGGGCTCCTCGGCTTC CGAACCAAAAGCCGCTTTTGGACTGAGAGAGGCGCGTCACGCGGGGCTCCGGGCTCCTCGGCTTC A C AC022217.4 Ensembl:ENSG00000253736 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:172770903..172771200 26863196 MeRIP-seq:(Medium) rs1433151854 Functional Loss SNV dbSNP153 33..33 33 - - - 62900 RMVar_ID_62900 Human_SNP_ID_261807258 m1A Human chr5 + 172771101 172771101 172771101 CGAACCAAAAGCCGCTTTTGGACTGAGAGAGGAGCGTCACGCGGGGCTCCGGGCTCCTCGGCTTC CGAACCAAAAGCCGCTTTTGGACTGAGAGAGGGGCGTCACGCGGGGCTCCGGGCTCCTCGGCTTC A G AC022217.4 Ensembl:ENSG00000253736 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:172770903..172771200 26863196 MeRIP-seq:(Medium) rs1433151854 Functional Loss SNV dbSNP153 33..33 33 - - - 62901 RMVar_ID_62901 Human_SNP_ID_261807275 m1A Human chr5 + 172771149 172771149 172771149 CCGGGCTCCTCGGCTTCTTCGCGGTTCCCCCGACTGCCCCTCCGACCCGCGTCGCACACACAGCC CCGGGCTCCTCGGCTTCTTCGCGGTTCCCCCGCCTGCCCCTCCGACCCGCGTCGCACACACAGCC A C AC022217.4 Ensembl:ENSG00000253736 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:172770844..172771200 26863196 MeRIP-seq:(Medium) rs1327638636 Functional Loss SNV dbSNP153 33..33 33 - - - 62902 RMVar_ID_62902 Human_SNP_ID_261823274 m1A Human chr5 - 172834379 172834379 172834379 TGCCGCCGCCGGGGGTGGGAGCGCTGCAGGCCAGGCGGGCCGCGGCGCCGCGTGGGTCCGAGCCC TGCCGCCGCCGGGGGTGGGAGCGCTGCAGGCCGGGCGGGCCGCGGCGCCGCGTGGGTCCGAGCCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:172834251..172834450 26863410 MeRIP-seq:(Medium) rs1045432348 Functional Loss SNV dbSNP153 33..33 33 - - - 62903 RMVar_ID_62903 Human_SNP_ID_261823275 m1A Human chr5 - 172834379 172834379 172834379 TGCCGCCGCCGGGGGTGGGAGCGCTGCAGGCCAGGCGGGCCGCGGCGCCGCGTGGGTCCGAGCCC TGCCGCCGCCGGGGGTGGGAGCGCTGCAGGCCCGGCGGGCCGCGGCGCCGCGTGGGTCCGAGCCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:172834251..172834450 26863410 MeRIP-seq:(Medium) rs1045432348 Functional Loss SNV dbSNP153 33..33 33 - - - 62904 RMVar_ID_62904 Human_SNP_ID_261828574 m1A Human chr5 + 172856121 172856121 172856121 AGGAGAGACCCTGAAGCACTTGAGGCCAGAGGAAGACATGCGCCTTGTCAGTGATCCCTGCATCC AGGAGAGACCCTGAAGCACTTGAGGCCAGAGGCAGACATGCGCCTTGTCAGTGATCCCTGCATCC A C ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172856115..172856209 26863196 MeRIP-seq:(Medium) rs765538827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236263,RMVar_hsa_circ_122533 62905 RMVar_ID_62905 Human_SNP_ID_261830440 m1A Human chr5 + 172863434 172863434 172863434 CAATCTGGGTTCCACCTAAAACCGTCTCAGGTACACCACTGCGCAGCCTCCCAGAACCACCCACC CAATCTGGGTTCCACCTAAAACCGTCTCAGGTGCACCACTGCGCAGCCTCCCAGAACCACCCACC A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:172863431..172863557 26863196 MeRIP-seq:(Medium) rs188654496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236263,RMVar_hsa_circ_122533 62906 RMVar_ID_62906 Human_SNP_ID_261838797 m1A Human chr5 + 172895694 172895694 172895694 AGCTCCACCTCTGGGAGTAGGGGAAGCTTCCCATCAAAAGGGACATGTGAGTCGGGCCTGGGAGG AGCTCCACCTCTGGGAGTAGGGGAAGCTTCCCGTCAAAAGGGACATGTGAGTCGGGCCTGGGAGG A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172895690..172895942 26863196 MeRIP-seq:(Medium) rs946038706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236266,RMVar_hsa_circ_362865,RMVar_hsa_circ_358914 62907 RMVar_ID_62907 Human_SNP_ID_261838807 m1A Human chr5 + 172895730 172895730 172895730 AAAGGGACATGTGAGTCGGGCCTGGGAGGATGAGTAGGAGTTCAGCAAGCAGAGAGGATAACCAT AAAGGGACATGTGAGTCGGGCCTGGGAGGATGCGTAGGAGTTCAGCAAGCAGAGAGGATAACCAT A C ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172895726..172895914 26863196 MeRIP-seq:(Medium) rs1197001265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236266,RMVar_hsa_circ_362865,RMVar_hsa_circ_358914 62908 RMVar_ID_62908 Human_SNP_ID_261843944 m1A Human chr5 + 172914827 172914827 172914827 ATGGGGCAGGCTGCCGCTTCGAGGGGCAGTTCAGCATCAACAAGGTATGGAAGCCCTGCCTCAGC ATGGGGCAGGCTGCCGCTTCGAGGGGCAGTTCGGCATCAACAAGGTATGGAAGCCCTGCCTCAGC A G ERGIC1 Ensembl:ENSG00000113719 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172914777..172914893 26863196 MeRIP-seq:(Medium) rs1335761988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249992,Human_RBP_ID_17303246,Human_RBP_ID_19124940 Human_Splice_Rec_721187,Human_Splice_Rec_721211,Human_Splice_Rec_721221,Human_Splice_Rec_721233,Human_Splice_Rec_721239,Human_Splice_Rec_721249,Human_Splice_Rec_721255 RMVar_hsa_circ_283903,RMVar_hsa_circ_124595,RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236266,RMVar_hsa_circ_358914,RMVar_hsa_circ_276196,RMVar_hsa_circ_236268,RMVar_hsa_circ_37037,RMVar_hsa_circ_342197,RMVar_hsa_circ_236267,RMVar_hsa_circ_376297,RMVar_hsa_circ_289094,RMVar_hsa_circ_236269,RMVar_hsa_circ_14638,RMVar_hsa_circ_283190,RMVar_hsa_circ_236270,RMVar_hsa_circ_236271,RMVar_hsa_circ_117339,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_326533,RMVar_hsa_circ_357326,RMVar_hsa_circ_236273 62909 RMVar_ID_62909 Human_SNP_ID_261844534 m1A Human chr5 - 172916971 172916971 172916971 TCCTTTTTTTGTTTGTTTTGAGATGGAGTCTCACTCTGTCGCCCAGACTGGAGTGCAGTGGTACG TCCTTTTTTTGTTTGTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGACTGGAGTGCAGTGGTACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172916969..172917213 26863196 MeRIP-seq:(Medium) rs751205875 Functional Loss SNV dbSNP153 33..33 33 - - - 62910 RMVar_ID_62910 Human_SNP_ID_261844536 m1A Human chr5 + 172916980 172916980 172916980 GCACTCCAGTCTGGGCGACAGAGTGAGACTCCATCTCAAAACAAACAAAAAAAGGATGGGGCTGG GCACTCCAGTCTGGGCGACAGAGTGAGACTCCGTCTCAAAACAAACAAAAAAAGGATGGGGCTGG A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172916978..172917114 26863196 MeRIP-seq:(Medium) rs1344907195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283903,RMVar_hsa_circ_124595,RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236268,RMVar_hsa_circ_37037,RMVar_hsa_circ_342197,RMVar_hsa_circ_376297,RMVar_hsa_circ_289094,RMVar_hsa_circ_236270,RMVar_hsa_circ_236271,RMVar_hsa_circ_117339,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_236273 62911 RMVar_ID_62911 Human_SNP_ID_261845061 m1A Human chr5 - 172919144 172919144 172919144 TTTATCAAAATCACATATTTCCTGTTTACCTGAGCACTGGCTGTCCCCCCGTTATAGAACATGGG TTTATCAAAATCACATATTTCCTGTTTACCTGGGCACTGGCTGTCCCCCCGTTATAGAACATGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172919142..172919219 26863196 MeRIP-seq:(Medium) rs779749348 Functional Loss SNV dbSNP153 33..33 33 - - - 62912 RMVar_ID_62912 Human_SNP_ID_261845325 m1A Human chr5 + 172920285 172920285 172920285 GAAGCCACCAGGGTCCATGTGCTGTGATGGCAAGGTCAGCAGCCAGCCCCCGCACCTCTCTCCCA GAAGCCACCAGGGTCCATGTGCTGTGATGGCAGGGTCAGCAGCCAGCCCCCGCACCTCTCTCCCA A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172920281..172920383 26863196 MeRIP-seq:(Medium) rs939505176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283903,RMVar_hsa_circ_124595,RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236268,RMVar_hsa_circ_37037,RMVar_hsa_circ_342197,RMVar_hsa_circ_376297,RMVar_hsa_circ_289094,RMVar_hsa_circ_236270,RMVar_hsa_circ_236271,RMVar_hsa_circ_117339,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_236273 62913 RMVar_ID_62913 Human_SNP_ID_261845327 m1A Human chr5 + 172920293 172920293 172920293 CAGGGTCCATGTGCTGTGATGGCAAGGTCAGCAGCCAGCCCCCGCACCTCTCTCCCAGCATCAGG CAGGGTCCATGTGCTGTGATGGCAAGGTCAGCCGCCAGCCCCCGCACCTCTCTCCCAGCATCAGG A C ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172920290..172920358 26863196 MeRIP-seq:(Medium) rs993589959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283903,RMVar_hsa_circ_124595,RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236268,RMVar_hsa_circ_37037,RMVar_hsa_circ_342197,RMVar_hsa_circ_376297,RMVar_hsa_circ_289094,RMVar_hsa_circ_236270,RMVar_hsa_circ_236271,RMVar_hsa_circ_117339,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_236273 62914 RMVar_ID_62914 Human_SNP_ID_261845864 m1A Human chr5 + 172922291 172922291 172922291 TCTTTTCTGTAAAATGGGAATTATCAGATGACAAAGTCAAAGGATTCAGTGTTGTTTGTTTAGTC TCTTTTCTGTAAAATGGGAATTATCAGATGACGAAGTCAAAGGATTCAGTGTTGTTTGTTTAGTC A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:172922289..172922636 26863196 MeRIP-seq:(Medium) rs946311719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3765371,Human_RBP_ID_10196130 RMVar_hsa_circ_283903,RMVar_hsa_circ_124595,RMVar_hsa_circ_236263,RMVar_hsa_circ_122533,RMVar_hsa_circ_236268,RMVar_hsa_circ_37037,RMVar_hsa_circ_342197,RMVar_hsa_circ_376297,RMVar_hsa_circ_289094,RMVar_hsa_circ_236270,RMVar_hsa_circ_236271,RMVar_hsa_circ_117339,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_236273 62915 RMVar_ID_62915 Human_SNP_ID_261846007 m1A Human chr5 - 172922841 172922841 172922841 TTCCCCACAGCCTGGGCCTTTTCCCAATAATGACTGTTAAGATCTTTTTAAACCCTACATCAGAT TTCCCCACAGCCTGGGCCTTTTCCCAATAATGCCTGTTAAGATCTTTTTAAACCCTACATCAGAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172922838..172923089 26863196 MeRIP-seq:(Medium) rs989052726 Functional Loss SNV dbSNP153 33..33 33 - - - 62916 RMVar_ID_62916 Human_SNP_ID_261848938 m1A Human chr5 - 172935144 172935142 172935144 GATATAAGAATCAGAAGTACAAACTGTGTCTCAGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC GATATAAGAATCAGAAGTACAAACTGTGTCTC__GGGGGGCGGGGACTGGATTGCAGAGGGCCCC CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172935138..172935355 26863196 MeRIP-seq:(Medium) rs757370376 Functional Loss DEL dbSNP153 33..34 33 - - - 62917 RMVar_ID_62917 Human_SNP_ID_261848942 m1A Human chr5 - 172935144 172935143 172935144 GATATAAGAATCAGAAGTACAAACTGTGTCTCAGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC GATATAAGAATCAGAAGTACAAACTGTGTCTC_GGGGGGGCGGGGACTGGATTGCAGAGGGCCCC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172935138..172935355 26863196 MeRIP-seq:(Medium) rs201862360 Functional Loss DEL dbSNP153 33..33 33 - - - 62918 RMVar_ID_62918 Human_SNP_ID_261848945 m1A Human chr5 - 172935144 172935144 172935144 GATATAAGAATCAGAAGTACAAACTGTGTCTCAGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC GATATAAGAATCAGAAGTACAAACTGTGTCTCTGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172935138..172935355 26863196 MeRIP-seq:(Medium) rs767253308 Functional Loss SNV dbSNP153 33..33 33 - - - 62919 RMVar_ID_62919 Human_SNP_ID_261848946 m1A Human chr5 - 172935144 172935144 172935144 GATATAAGAATCAGAAGTACAAACTGTGTCTCAGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC GATATAAGAATCAGAAGTACAAACTGTGTCTCGGGGGGGGCGGGGACTGGATTGCAGAGGGCCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172935138..172935355 26863196 MeRIP-seq:(Medium) rs767253308 Functional Loss SNV dbSNP153 33..33 33 - - - 62920 RMVar_ID_62920 Human_SNP_ID_261848985 m1A Human chr5 + 172935218 172935218 172935218 AGGAATACGTCGCCTACAGCCACACGGGCCGCATCATCCCTGCAATCTGGTTCCGCTACGACCTC AGGAATACGTCGCCTACAGCCACACGGGCCGCCTCATCCCTGCAATCTGGTTCCGCTACGACCTC A C ERGIC1 Ensembl:ENSG00000113719 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172935133..172935217 26863196 MeRIP-seq:(Medium) rs1402145698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_945464,Human_RBP_ID_17299401,Human_RBP_ID_17412886,Human_RBP_ID_19016130 Human_Splice_Rec_721194,Human_Splice_Rec_721195,Human_Splice_Rec_721281 RMVar_hsa_circ_4160,RMVar_hsa_circ_37037,RMVar_hsa_circ_289094,RMVar_hsa_circ_236271,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_368223,RMVar_hsa_circ_236274,RMVar_hsa_circ_236278,RMVar_hsa_circ_302521,RMVar_hsa_circ_236279 62921 RMVar_ID_62921 Human_SNP_ID_261848986 m1A Human chr5 + 172935218 172935218 172935218 AGGAATACGTCGCCTACAGCCACACGGGCCGCATCATCCCTGCAATCTGGTTCCGCTACGACCTC AGGAATACGTCGCCTACAGCCACACGGGCCGCGTCATCCCTGCAATCTGGTTCCGCTACGACCTC A G ERGIC1 Ensembl:ENSG00000113719 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172935133..172935217 26863196 MeRIP-seq:(Medium) rs1402145698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_945464,Human_RBP_ID_17299401,Human_RBP_ID_17412886,Human_RBP_ID_19016130 Human_Splice_Rec_721194,Human_Splice_Rec_721195,Human_Splice_Rec_721281 RMVar_hsa_circ_4160,RMVar_hsa_circ_37037,RMVar_hsa_circ_289094,RMVar_hsa_circ_236271,RMVar_hsa_circ_236272,RMVar_hsa_circ_89386,RMVar_hsa_circ_357326,RMVar_hsa_circ_368223,RMVar_hsa_circ_236274,RMVar_hsa_circ_236278,RMVar_hsa_circ_302521,RMVar_hsa_circ_236279 62922 RMVar_ID_62922 Human_SNP_ID_261852846 m1A Human chr5 + 172950686 172950686 172950686 TTCATCCTCCAGCACTGACTTCTGACACTCCCACCCCACCCCTGCCCTCTTGCAGATCTGTGCCA TTCATCCTCCAGCACTGACTTCTGACACTCCCTCCCCACCCCTGCCCTCTTGCAGATCTGTGCCA A T ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172950683..172950866 26863196 MeRIP-seq:(Medium) rs1244191256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944785 62923 RMVar_ID_62923 Human_SNP_ID_261855173 m1A Human chr5 + 172958757 172958757 172958757 GGTCGGCGAACGAAACGCGGAGCTCGGGAGCGACCCGGCGGGGCCAGGCACGGGCAGAAGGGCCA GGTCGGCGAACGAAACGCGGAGCTCGGGAGCGGCCCGGCGGGGCCAGGCACGGGCAGAAGGGCCA A G RPL26L1 Ensembl:ENSG00000037241 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172958714..172958792 26863196 MeRIP-seq:(Medium) rs1197216739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_721307 62924 RMVar_ID_62924 Human_SNP_ID_261855472 m1A Human chr5 + 172959502 172959502 172959502 TGAGTGGAGGCTGGAGTTTTCTCGGACAGTGAACTCTACCGCCCCGTGAGACCCTGCCCTATGTG TGAGTGGAGGCTGGAGTTTTCTCGGACAGTGATCTCTACCGCCCCGTGAGACCCTGCCCTATGTG A T RPL26L1 Ensembl:ENSG00000037241 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172959497..172959620 26863196 MeRIP-seq:(Medium) rs1468077723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_721325 62925 RMVar_ID_62925 Human_SNP_ID_261855611 m1A Human chr5 - 172959928 172959928 172959928 GATCTTCCTGCGCACGTGTGAGGGGGCATTGAAGTGACGTTTGCGGTTTTTACTGCGGTCCGAGG GATCTTCCTGCGCACGTGTGAGGGGGCATTGAGGTGACGTTTGCGGTTTTTACTGCGGTCCGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:172959823..172959961 26863196 MeRIP-seq:(Medium) rs776266591 Functional Loss SNV dbSNP153 33..33 33 - - - 62926 RMVar_ID_62926 Human_SNP_ID_261862352 m1A Human chr5 + 172983861 172983861 172983861 ACGGGGTAGGGGTTGGCGCTCAGGCGGCGACCATGGCGTATCACGGCCTCACTGTGCCTCTCATT ACGGGGTAGGGGTTGGCGCTCAGGCGGCGACCGTGGCGTATCACGGCCTCACTGTGCCTCTCATT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172983776..172984010 26863196 MeRIP-seq:(Medium) rs1257079895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4822409,Human_RBP_ID_5326646,Human_RBP_ID_9335455,Human_RBP_ID_22459032,Human_RBP_ID_24097025 Human_miRNA_ID_2503519 RMVar_hsa_circ_236281,RMVar_hsa_circ_127736 62927 RMVar_ID_62927 Human_SNP_ID_261862367 m1A Human chr5 + 172983891 172983891 172983891 CCATGGCGTATCACGGCCTCACTGTGCCTCTCATTGTGATGAGCGTGTTCTGGGGCTTCGTCGGC CCATGGCGTATCACGGCCTCACTGTGCCTCTCGTTGTGATGAGCGTGTTCTGGGGCTTCGTCGGC A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:172983801..172983954 26863196 MeRIP-seq:(Medium) rs1379298649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1650347,Human_RBP_ID_2917800,Human_RBP_ID_4822409,Human_RBP_ID_5326646,Human_RBP_ID_9335455 Human_Splice_Rec_721337,Human_Splice_Rec_721343,Human_Splice_Rec_721347,Human_Splice_Rec_721351 Human_miRNA_ID_2909150 RMVar_hsa_circ_236281,RMVar_hsa_circ_127736 62928 RMVar_ID_62928 Human_SNP_ID_261880238 m1A Human chr5 + 173056628 173056628 173056628 CCGGCGCGGGGCGGGGGCCGGGACCACGGCCGAGTGCTAGGGCGCGCGGGCCTTGGGCCACCGCC CCGGCGCGGGGCGGGGGCCGGGACCACGGCCGGGTGCTAGGGCGCGCGGGCCTTGGGCCACCGCC A G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173056611..173056733 26863196 MeRIP-seq:(Medium) rs1035152423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783901,Human_RBP_ID_5395831 62929 RMVar_ID_62929 Human_SNP_ID_261880300 m1A Human chr5 - 173056817 173056814 173056817 CAGCAGCGGCCCCGGGCTCGGAGGCAGCGGGGAAGGGCCGGGCGGCCCGGCAGGACGGACGCCCG CAGCAGCGGCCCCGGGCTCGGAGGCAGCGGGG___GGCCGGGCGGCCCGGCAGGACGGACGCCCG CCTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:173056810..173056876 26863196 MeRIP-seq:(Medium) rs1190480972 Functional Loss DEL dbSNP153 33..35 33 - - - 62930 RMVar_ID_62930 Human_SNP_ID_261880347 m1A Human chr5 + 173056928 173056928 173056928 GAGGGGAGGGGAGGCGAGACTGGCGGGGGAGGAGGGGAGAGAGGGGCGTGTGAGGAAGGGCCGGG GAGGGGAGGGGAGGCGAGACTGGCGGGGGAGGGGGGGAGAGAGGGGCGTGTGAGGAAGGGCCGGG A G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173056925..173057127 26863196 MeRIP-seq:(Medium) rs1039855176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8236747,Human_RBP_ID_8894265,Human_RBP_ID_26791808 62931 RMVar_ID_62931 Human_SNP_ID_261880348 m1A Human chr5 + 173056928 173056928 173056928 GAGGGGAGGGGAGGCGAGACTGGCGGGGGAGGAGGGGAGAGAGGGGCGTGTGAGGAAGGGCCGGG GAGGGGAGGGGAGGCGAGACTGGCGGGGGAGGTGGGGAGAGAGGGGCGTGTGAGGAAGGGCCGGG A T CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173056925..173057127 26863196 MeRIP-seq:(Medium) rs1039855176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8236747,Human_RBP_ID_8894265,Human_RBP_ID_26791808 62932 RMVar_ID_62932 Human_SNP_ID_261880351 m1A Human chr5 + 173056937 173056932 173056937 GGAGGCGAGACTGGCGGGGGAGGAGGGGAGAGAGGGGCGTGTGAGGAAGGGCCGGGGCCGCGGAG GGAGGCGAGACTGGCGGGGGAGGAGGGG_____GGGGCGTGTGAGGAAGGGCCGGGGCCGCGGAG GAGAGA G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:173056930..173057294 26863196 MeRIP-seq:(Medium) rs1398997454 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_3782960,Human_RBP_ID_5326647,Human_RBP_ID_8214220,Human_RBP_ID_8236747,Human_RBP_ID_8894265,Human_RBP_ID_9335456,Human_RBP_ID_9436976,Human_RBP_ID_26791808 62933 RMVar_ID_62933 Human_SNP_ID_261880522 m1A Human chr5 + 173057362 173057362 173057362 CACTGAGAGGGGAGGAGACAGGGCAAAGGGCGAGGGAGCCGGGCCGGGGGTGTTTCGGGTGTCCG CACTGAGAGGGGAGGAGACAGGGCAAAGGGCGGGGGAGCCGGGCCGGGGGTGTTTCGGGTGTCCG A G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173057352..173057437 26863196 MeRIP-seq:(Medium) rs1362217837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3782962,Human_RBP_ID_5326648,Human_RBP_ID_17662626 62934 RMVar_ID_62934 Human_SNP_ID_261886541 m1A Human chr5 + 173080536 173080536 173080536 TTTTCAAAAGTCAACTTTTTTTTTGAAACATCAACTTGTTTTTCCTGGAATTCAGTGAAGTTACT TTTTCAAAAGTCAACTTTTTTTTTGAAACATCGACTTGTTTTTCCTGGAATTCAGTGAAGTTACT A G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:173080535..173080616;chr5:173080535..173080644 26863196 MeRIP-seq:(Medium) rs1323919602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22680986 62935 RMVar_ID_62935 Human_SNP_ID_261889375 m1A Human chr5 - 173091317 173091317 173091317 CTCTTCCTCTTCTTCCTCCTCCTCATTTTCAGACAGTTCATGCTCACTGCCGAATCCTTCATCAT CTCTTCCTCTTCTTCCTCCTCCTCATTTTCAGGCAGTTCATGCTCACTGCCGAATCCTTCATCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:173091267..173091392 26863196 MeRIP-seq:(Medium) rs771417520 Functional Loss SNV dbSNP153 33..33 33 - - - 62936 RMVar_ID_62936 Human_SNP_ID_261893514 m1A Human chr5 + 173108580 173108580 173108580 GAAGGGGTCTTTTCATTTGTTCTGATTGATTTATTGAAATTTATGGAGCTTAAAAATTGCGGGAC GAAGGGGTCTTTTCATTTGTTCTGATTGATTTGTTGAAATTTATGGAGCTTAAAAATTGCGGGAC A G CREBRF Ensembl:ENSG00000164463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:173108579..173108659 26863196 MeRIP-seq:(Medium) rs747386867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335667,RMVar_hsa_circ_367542,RMVar_hsa_circ_306840,RMVar_hsa_circ_236287,RMVar_hsa_circ_268749 62937 RMVar_ID_62937 Human_SNP_ID_261924787 m1A Human chr5 + 173232607 173232607 173232607 GGCTCGGATACCATGCAGCGTGGACACTCCCGAGTTGCTCTGCGGAATCCCGGGGCTCTGAACCG GGCTCGGATACCATGCAGCGTGGACACTCCCGGGTTGCTCTGCGGAATCCCGGGGCTCTGAACCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:173232557..173232956 32194978 MeRIP-seq:(Medium) rs777867699 Functional Loss SNV dbSNP153 33..33 33 - - - 62938 RMVar_ID_62938 Human_SNP_ID_261925806 m1A Human chr5 + 173234852 173234852 173234852 GGCGGGAAAGGCAGACGCACACTTGGCCGGTGAAGGCGCGCGGCCCAGCTCTGCGCGCAGCTCTG GGCGGGAAAGGCAGACGCACACTTGGCCGGTGGAGGCGCGCGGCCCAGCTCTGCGCGCAGCTCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:173234808..173235108 32194978 MeRIP-seq:(Medium) rs749763672 Functional Loss SNV dbSNP153 33..33 33 - - - 62939 RMVar_ID_62939 Human_SNP_ID_261946600 m1A Human chr5 - 173318073 173318073 173318073 GCCTCCCACGGCGCCCCCCGAGCGCCAGCCCCAGGTGGACAGAACCAAGCTCTCCAGGGCCCACC GCCTCCCACGGCGCCCCCCGAGCGCCAGCCCCTGGTGGACAGAACCAAGCTCTCCAGGGCCCACC T A STC2 Ensembl:ENSG00000113739 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173318026..173318161 26863196 MeRIP-seq:(Medium) rs1299923955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8610507,Human_RBP_ID_22459367,Human_RBP_ID_22771788,Human_RBP_ID_27513953 RMVar_hsa_circ_236294,RMVar_hsa_circ_111967,RMVar_hsa_circ_116248,RMVar_hsa_circ_80495,RMVar_hsa_circ_236295,RMVar_hsa_circ_236293 62940 RMVar_ID_62940 Human_SNP_ID_261947485 m1A Human chr5 - 173321537 173321537 173321537 TCCTAGACCTGAAAGGGCTCACAGCTCCCCACATGTGGTGGGCTTCTTGTCCTTTTATCAAATAT TCCTAGACCTGAAAGGGCTCACAGCTCCCCACCTGTGGTGGGCTTCTTGTCCTTTTATCAAATAT T G STC2 Ensembl:ENSG00000113739 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4867699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_637890 GWAS_ID_7687,GWAS_ID_7688 RMVar_hsa_circ_236294,RMVar_hsa_circ_116248,RMVar_hsa_circ_80495,RMVar_hsa_circ_236295 62941 RMVar_ID_62941 Human_SNP_ID_261948578 m1A Human chr5 - 173325919 173325919 173325919 TTCGAGAACAACTCTTGTGAGATTCGGGGCTTACATGGGATTTGCATGACTTTTCTGCACAACGC TTCGAGAACAACTCTTGTGAGATTCGGGGCTTGCATGGGATTTGCATGACTTTTCTGCACAACGC T C STC2 Ensembl:ENSG00000113739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:173325851..173326025 32194978 MeRIP-seq:(Medium) rs1024272834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1650540,Human_RBP_ID_1992414,Human_RBP_ID_3765536,Human_RBP_ID_7417668,Human_RBP_ID_8610541,Human_RBP_ID_8888126,Human_RBP_ID_15384886,Human_RBP_ID_18044736,Human_RBP_ID_18356650,Human_RBP_ID_18838465,Human_RBP_ID_22771793,Human_RBP_ID_24097275,Human_RBP_ID_27513969 Human_Splice_Rec_721454,Human_Splice_Rec_721455,Human_Splice_Rec_721464,Human_Splice_Rec_721465,Human_Splice_Rec_721468,Human_Splice_Rec_721469,Human_Splice_Rec_721472 RMVar_hsa_circ_80495,RMVar_hsa_circ_236295 62942 RMVar_ID_62942 Human_SNP_ID_261949237 m1A Human chr5 + 173328356 173328356 173328356 CCTCGCGGCCGCGGCTCGGATAGAGGTTACCCAGCGCCCTCCCGTAGCTCTCCGGAGAGCATGTG CCTCGCGGCCGCGGCTCGGATAGAGGTTACCCTGCGCCCTCCCGTAGCTCTCCGGAGAGCATGTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:173328101..173328507;chr5:173328076..173328457 26863196 MeRIP-seq:(Medium) rs1378263900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1650571 62943 RMVar_ID_62943 Human_SNP_ID_262018140 m1A Human chr5 + 173616407 173616407 173616407 GCCTGGCTAGTTCCGCCGCCGCCCACCGCGCCAGTTCCCCCGCCGCCGCCGCCGTCCGCCATGGC GCCTGGCTAGTTCCGCCGCCGCCCACCGCGCCGGTTCCCCCGCCGCCGCCGCCGTCCGCCATGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:173616298..173616590 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 62944 RMVar_ID_62944 Human_SNP_ID_262018224 m1A Human chr5 - 173616587 173616576 173616588 TATCAGAGGGGGCCTTCGCCGCCGCCGCCCCCACCACCGCCCCTGCCGCCATCGCCACCTCCGCC TATCAGAGGGGGCCTTCGCCGCCGCCGCCCC____________TGCCGCCATCGCCACCTCCGCC AGGGGCGGTGGTG A BOD1 Ensembl:ENSG00000145919 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:173616501..173616650 26863410 MeRIP-seq:(Medium) rs1358654932 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_4846881 RMVar_hsa_circ_236296,RMVar_hsa_circ_96853 62945 RMVar_ID_62945 Human_SNP_ID_262018235 m1A Human chr5 - 173616587 173616587 173616587 TATCAGAGGGGGCCTTCGCCGCCGCCGCCCCCACCACCGCCCCTGCCGCCATCGCCACCTCCGCC TATCAGAGGGGGCCTTCGCCGCCGCCGCCCCCGCCACCGCCCCTGCCGCCATCGCCACCTCCGCC T C BOD1 Ensembl:ENSG00000145919 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:173616501..173616650 26863410 MeRIP-seq:(Medium) rs963447554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846881 RMVar_hsa_circ_236296,RMVar_hsa_circ_96853 62946 RMVar_ID_62946 Human_SNP_ID_262018236 m1A Human chr5 - 173616587 173616587 173616587 TATCAGAGGGGGCCTTCGCCGCCGCCGCCCCCACCACCGCCCCTGCCGCCATCGCCACCTCCGCC TATCAGAGGGGGCCTTCGCCGCCGCCGCCCCCCCCACCGCCCCTGCCGCCATCGCCACCTCCGCC T G BOD1 Ensembl:ENSG00000145919 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:173616501..173616650 26863410 MeRIP-seq:(Medium) rs963447554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846881 RMVar_hsa_circ_236296,RMVar_hsa_circ_96853 62947 RMVar_ID_62947 Human_SNP_ID_262018254 m1A Human chr5 + 173616604 173616597 173616604 CGGCAGGGGCGGTGGTGGGGGCGGCGGCGGCGAAGGCCCCCTCTGATACAGCAGAGGTTGTGGTG CGGCAGGGGCGGTGGTGGGGGCGGCG_______AGGCCCCCTCTGATACAGCAGAGGTTGTGGTG GGCGGCGA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr5:173616368..173616675;chr5:173616520..173616627 26863410 MeRIP-seq:(Medium) rs1392794975 Functional Loss DEL dbSNP153 27..33 33 - - - 62948 RMVar_ID_62948 Human_SNP_ID_262018262 m1A Human chr5 + 173616605 173616605 173616605 GGCAGGGGCGGTGGTGGGGGCGGCGGCGGCGAAGGCCCCCTCTGATACAGCAGAGGTTGTGGTGG GGCAGGGGCGGTGGTGGGGGCGGCGGCGGCGAGGGCCCCCTCTGATACAGCAGAGGTTGTGGTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:173616362..173616650 26863196 MeRIP-seq:(Medium) rs1046972513 Functional Loss SNV dbSNP153 33..33 33 - - - 62949 RMVar_ID_62949 Human_SNP_ID_262041782 m1A Human chr5 + 173708964 173708964 173708964 CAGCCATCTCCTCCCGGCCTCCATCCTCACCCACTCCATTTCAGTCTCTGTTTGGCCCCCAGCTG CAGCCATCTCCTCCCGGCCTCCATCCTCACCCCCTCCATTTCAGTCTCTGTTTGGCCCCCAGCTG A C LINC01942,LINC01942:2 RNACentral:URS0000D571C0,RNACentral:URS0000D59494 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173708914..173709003 26863196 MeRIP-seq:(Medium) rs1012439411 Functional Loss SNV dbSNP153 33..33 33 - - - 62950 RMVar_ID_62950 Human_SNP_ID_262047483 m1A Human chr5 - 173731146 173731146 173731146 TGGGCCGGGGCAGGTCCCAGCTGGACTGGGTGAGGTGACGGGCCTGTGGGGAGCTGAAGGTCTGA TGGGCCGGGGCAGGTCCCAGCTGGACTGGGTGCGGTGACGGGCCTGTGGGGAGCTGAAGGTCTGA T G LINC01484 Ensembl:ENSG00000253686 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:173731060..173731267 26863196 MeRIP-seq:(Medium) rs1474054677 Functional Loss SNV dbSNP153 33..33 33 - - - 62951 RMVar_ID_62951 Human_SNP_ID_262049336 m1A Human chr5 - 173737498 173737498 173737498 AGGTCCCTAAGGAGATGACTTACAATGTGGCCAGAATGAGGAGAAAGGGCCAGCCCAGGGGAGAA AGGTCCCTAAGGAGATGACTTACAATGTGGCCCGAATGAGGAGAAAGGGCCAGCCCAGGGGAGAA T G LINC01484 Ensembl:ENSG00000253686 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:173737453..173737561 26863196 MeRIP-seq:(Medium) rs1163300650 Functional Loss SNV dbSNP153 33..33 33 - - - 62952 RMVar_ID_62952 Human_SNP_ID_262051508 m1A Human chr5 + 173746146 173746146 173746146 CAACAGCTGATCTTCACAGATGTGGGACAGAAAGTCATCCCTCTGCTCACCTGAAGCAAATGCCT CAACAGCTGATCTTCACAGATGTGGGACAGAACGTCATCCCTCTGCTCACCTGAAGCAAATGCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:173746021..173746184 26863196 MeRIP-seq:(Medium) rs114813892 Functional Loss SNV dbSNP153 33..33 33 - - - 62953 RMVar_ID_62953 Human_SNP_ID_262088105 m1A Human chr5 - 173888413 173888413 173888413 CTGTCGCCGCTGCTGCCGCCGCCGCCGCCGCCACCGCCTCCCGGTGCCCGGGTCCCGCAGCCGCG CTGTCGCCGCTGCTGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGTGCCCGGGTCCCGCAGCCGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:173888351..173888575 26863196 MeRIP-seq:(Medium) rs1437994670 Functional Loss SNV dbSNP153 33..33 33 - - - 62954 RMVar_ID_62954 Human_SNP_ID_262088251 m1A Human chr5 + 173888926 173888926 173888926 ACCCCCGCAAGAGGGAGAAACGGGTGTTTCCAACCCCTTTCATGGGGGAGAGGAAGCCGCGGGGA ACCCCCGCAAGAGGGAGAAACGGGTGTTTCCAGCCCCTTTCATGGGGGAGAGGAAGCCGCGGGGA A G CPEB4 Ensembl:ENSG00000113742 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:173888901..173888925 26863196 MeRIP-seq:(Medium) rs993435915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532119 62955 RMVar_ID_62955 Human_SNP_ID_262088252 m1A Human chr5 + 173888926 173888926 173888926 ACCCCCGCAAGAGGGAGAAACGGGTGTTTCCAACCCCTTTCATGGGGGAGAGGAAGCCGCGGGGA ACCCCCGCAAGAGGGAGAAACGGGTGTTTCCATCCCCTTTCATGGGGGAGAGGAAGCCGCGGGGA A T CPEB4 Ensembl:ENSG00000113742 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:173888901..173888925 26863196 MeRIP-seq:(Medium) rs993435915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532119 62956 RMVar_ID_62956 Human_SNP_ID_262088736 m1A Human chr5 + 173890688 173890688 173890688 GCTGGGGAGGTTCCCAAGGCCGAGATCACCGCAGAGGGCTGAATGGTGGAATAACGCCCCTGAAC GCTGGGGAGGTTCCCAAGGCCGAGATCACCGCGGAGGGCTGAATGGTGGAATAACGCCCCTGAAC A G CPEB4 Ensembl:ENSG00000113742 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:173890644..173890740 26863196 MeRIP-seq:(Medium) rs759880283 Functional Loss SNV dbSNP153 33..33 33 - - - 62957 RMVar_ID_62957 Human_SNP_ID_262100860 m1A Human chr5 - 173947409 173947409 173947409 ACCATACGTACTGCTGCTCAGGCCTCTGAGCAAGCCCCCTCTACATACATTCATACACATCCCCT ACCATACGTACTGCTGCTCAGGCCTCTGAGCAGGCCCCCTCTACATACATTCATACACATCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:173947398..173947525 26863196 MeRIP-seq:(Medium) rs907450820 Functional Loss SNV dbSNP153 33..33 33 - - - 62958 RMVar_ID_62958 Human_SNP_ID_262246371 m1A Human chr5 + 174522065 174522057 174522065 AAAGAGAGACAGAGTGTGTGTGTGTGTGAGAGAGAGAAGACAGAGAGACAGAGTGTGTGTGTGTG AAAGAGAGACAGAGTGTGTGTGTGT________GAGAAGACAGAGAGACAGAGTGTGTGTGTGTG TGTGAGAGA T LINC01411 Ensembl:ENSG00000249306 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:174521680..174522512 26863196 MeRIP-seq:(Medium) rs1342809592 Functional Loss DEL dbSNP153 26..33 33 - - - 62959 RMVar_ID_62959 Human_SNP_ID_262246384 m1A Human chr5 + 174522069 174522068 174522069 AGAGACAGAGTGTGTGTGTGTGTGAGAGAGAGAAGACAGAGAGACAGAGTGTGTGTGTGTGAGAG AGAGACAGAGTGTGTGTGTGTGTGAGAGAGAG_AGACAGAGAGACAGAGTGTGTGTGTGTGAGAG GA G LINC01411 Ensembl:ENSG00000249306 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:174521695..174522537 26863196 MeRIP-seq:(Medium) rs1364183330 Functional Loss DEL dbSNP153 33..33 33 - - - 62960 RMVar_ID_62960 Human_SNP_ID_262246579 m1A Human chr5 + 174522258 174522254 174522258 GAGAAGAAAGAGAGACAGAGTGTGTGTGTGAGAGAGACAGAGAGAGAAGACAGACAGTGTGTGTG GAGAAGAAAGAGAGACAGAGTGTGTGTGT____GAGACAGAGAGAGAAGACAGACAGTGTGTGTG TGAGA T LINC01411 Ensembl:ENSG00000249306 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:174522209..174522298 26863196 MeRIP-seq:(Medium) rs1207915806 Functional Loss DEL dbSNP153 30..33 33 - - - 62961 RMVar_ID_62961 Human_SNP_ID_262249029 m1A Human chr5 - 174530800 174530800 174530800 GCTCACCTTCCCATATGCACCCACCTGTATCCAATCCATACGCTCACCCTCCCATATGCACCCAT GCTCACCTTCCCATATGCACCCACCTGTATCCGATCCATACGCTCACCCTCCCATATGCACCCAT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:174530779..174530926 26863196 MeRIP-seq:(Medium) rs962280577 Functional Loss SNV dbSNP153 33..33 33 - - - 62962 RMVar_ID_62962 Human_SNP_ID_262299384 m1A Human chr5 + 174724731 174724731 174724731 GACGAGGAGGGCCCAGCAGTGGTGGCCGGACCAGGCCCGGGGCCTGGGGGCGCCGAGGGGGCCGC GACGAGGAGGGCCCAGCAGTGGTGGCCGGACCGGGCCCGGGGCCTGGGGGCGCCGAGGGGGCCGC A G MSX2 Ensembl:ENSG00000120149 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:174724631..174724780 26863410 MeRIP-seq:(Medium) rs1418090478 Functional Loss SNV dbSNP153 33..33 33 - - - 62963 RMVar_ID_62963 Human_SNP_ID_262487615 m1A Human chr5 + 175478625 175478625 175478625 ACTGAGCGGGACCTGCGAGCAGCGCGGGCGGCAGCCCGGGGGAAGCGGTGAGTCGCGGGCGGCAG ACTGAGCGGGACCTGCGAGCAGCGCGGGCGGCCGCCCGGGGGAAGCGGTGAGTCGCGGGCGGCAG A C SFXN1 Ensembl:ENSG00000164466 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:175478583..175478717 26863196 MeRIP-seq:(Medium) rs1405247383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788290,Human_RBP_ID_3968418,Human_RBP_ID_4846164,Human_RBP_ID_22460320,Human_RBP_ID_23050362 Human_Splice_Rec_721973,Human_Splice_Rec_721993,Human_Splice_Rec_721997,Human_Splice_Rec_721999,Human_Splice_Rec_722001,Human_Splice_Rec_722009,Human_Splice_Rec_722027,Human_Splice_Rec_722033 RMVar_hsa_circ_92872,RMVar_hsa_circ_236314 62964 RMVar_ID_62964 Human_SNP_ID_262491096 m1A Human chr5 + 175492161 175492161 175492161 TTAACATCAAGGAACCTCGATGGGATCAAAGCACTTTCATTGGACGAGCCAATCATTTCTTCACT TTAACATCAAGGAACCTCGATGGGATCAAAGCCCTTTCATTGGACGAGCCAATCATTTCTTCACT A C SFXN1 Ensembl:ENSG00000164466 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:175492076..175492200;chr5:175492066..175492225;chr5:175492060..175492250;chr5:175492040..175492200 26863196 MeRIP-seq:(Medium) rs1380916895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1650721,Human_RBP_ID_1992469,Human_RBP_ID_3765685,Human_RBP_ID_5477059,Human_RBP_ID_7418458,Human_RBP_ID_8610708,Human_RBP_ID_9398685,Human_RBP_ID_15386449,Human_RBP_ID_17299547,Human_RBP_ID_17412992,Human_RBP_ID_17529130,Human_RBP_ID_18044909,Human_RBP_ID_18170724,Human_RBP_ID_18448527,Human_RBP_ID_26353071,Human_RBP_ID_27078179 Human_Splice_Rec_721968,Human_Splice_Rec_721974,Human_Splice_Rec_721994,Human_Splice_Rec_721998,Human_Splice_Rec_722002,Human_Splice_Rec_722010,Human_Splice_Rec_722028,Human_Splice_Rec_722036 Human_miRNA_ID_1941796,Human_miRNA_ID_1944842,Human_miRNA_ID_2115987,Human_miRNA_ID_2199560,Human_miRNA_ID_2202627,Human_miRNA_ID_2315057,Human_miRNA_ID_2318217,Human_miRNA_ID_2321374,Human_miRNA_ID_2324531,Human_miRNA_ID_2327674,Human_miRNA_ID_2518910,Human_miRNA_ID_2522082,Human_miRNA_ID_2815090,Human_miRNA_ID_2821276,Human_miRNA_ID_2827409,Human_miRNA_ID_2830559,Human_miRNA_ID_2834678,Human_miRNA_ID_2840042,Human_miRNA_ID_2842882,Human_miRNA_ID_2862353,Human_miRNA_ID_3112079 RMVar_hsa_circ_92872,RMVar_hsa_circ_17586,RMVar_hsa_circ_277793,RMVar_hsa_circ_236314,RMVar_hsa_circ_300266,RMVar_hsa_circ_54925,RMVar_hsa_circ_236315,RMVar_hsa_circ_12696,RMVar_hsa_circ_236316 62965 RMVar_ID_62965 Human_SNP_ID_262491097 m1A Human chr5 + 175492161 175492161 175492161 TTAACATCAAGGAACCTCGATGGGATCAAAGCACTTTCATTGGACGAGCCAATCATTTCTTCACT TTAACATCAAGGAACCTCGATGGGATCAAAGCGCTTTCATTGGACGAGCCAATCATTTCTTCACT A G SFXN1 Ensembl:ENSG00000164466 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:175492076..175492200;chr5:175492066..175492225;chr5:175492060..175492250;chr5:175492040..175492200 26863196 MeRIP-seq:(Medium) rs1380916895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1650721,Human_RBP_ID_1992469,Human_RBP_ID_3765685,Human_RBP_ID_5477059,Human_RBP_ID_7418458,Human_RBP_ID_8610708,Human_RBP_ID_9398685,Human_RBP_ID_15386449,Human_RBP_ID_17299547,Human_RBP_ID_17412992,Human_RBP_ID_17529130,Human_RBP_ID_18044909,Human_RBP_ID_18170724,Human_RBP_ID_18448527,Human_RBP_ID_26353071,Human_RBP_ID_27078179 Human_Splice_Rec_721968,Human_Splice_Rec_721974,Human_Splice_Rec_721994,Human_Splice_Rec_721998,Human_Splice_Rec_722002,Human_Splice_Rec_722010,Human_Splice_Rec_722028,Human_Splice_Rec_722036 Human_miRNA_ID_1941796,Human_miRNA_ID_1944842,Human_miRNA_ID_2115987,Human_miRNA_ID_2199560,Human_miRNA_ID_2202627,Human_miRNA_ID_2315057,Human_miRNA_ID_2318217,Human_miRNA_ID_2321374,Human_miRNA_ID_2324531,Human_miRNA_ID_2327674,Human_miRNA_ID_2518910,Human_miRNA_ID_2522082,Human_miRNA_ID_2815090,Human_miRNA_ID_2821276,Human_miRNA_ID_2827409,Human_miRNA_ID_2830559,Human_miRNA_ID_2834678,Human_miRNA_ID_2840042,Human_miRNA_ID_2842882,Human_miRNA_ID_2862353,Human_miRNA_ID_3112079 RMVar_hsa_circ_92872,RMVar_hsa_circ_17586,RMVar_hsa_circ_277793,RMVar_hsa_circ_236314,RMVar_hsa_circ_300266,RMVar_hsa_circ_54925,RMVar_hsa_circ_236315,RMVar_hsa_circ_12696,RMVar_hsa_circ_236316 62966 RMVar_ID_62966 Human_SNP_ID_262496959 m1A Human chr5 + 175513811 175513811 175513811 GGGCTAGGGCGTGTGGGTAGGGCAGCCGGGGAAGAGCACTGGGTGGAGGTGTGGGAGTGAGCCAA GGGCTAGGGCGTGTGGGTAGGGCAGCCGGGGAGGAGCACTGGGTGGAGGTGTGGGAGTGAGCCAA A G SFXN1 Ensembl:ENSG00000164466 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:175513805..175513965 26863196 MeRIP-seq:(Medium) rs1561672141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839201,Human_RBP_ID_7418529,Human_RBP_ID_9436619,Human_RBP_ID_18956275 RMVar_hsa_circ_54925,RMVar_hsa_circ_12696,RMVar_hsa_circ_236323,RMVar_hsa_circ_86081,RMVar_hsa_circ_364042,RMVar_hsa_circ_236319,RMVar_hsa_circ_96105,RMVar_hsa_circ_236320,RMVar_hsa_circ_236321,RMVar_hsa_circ_373432,RMVar_hsa_circ_84304,RMVar_hsa_circ_236324,RMVar_hsa_circ_345385,RMVar_hsa_circ_294856 62967 RMVar_ID_62967 Human_SNP_ID_262496970 m1A Human chr5 + 175513843 175513843 175513843 AGAGCACTGGGTGGAGGTGTGGGAGTGAGCCAAGTGGGTATCGGTGATGAATATTCTGGCAGAGG AGAGCACTGGGTGGAGGTGTGGGAGTGAGCCAGGTGGGTATCGGTGATGAATATTCTGGCAGAGG A G SFXN1 Ensembl:ENSG00000164466 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:175513730..175514009 26863196 MeRIP-seq:(Medium) rs960378400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839201,Human_RBP_ID_9436619,Human_RBP_ID_15386692,Human_RBP_ID_18956275 RMVar_hsa_circ_54925,RMVar_hsa_circ_12696,RMVar_hsa_circ_236323,RMVar_hsa_circ_86081,RMVar_hsa_circ_364042,RMVar_hsa_circ_236319,RMVar_hsa_circ_96105,RMVar_hsa_circ_236320,RMVar_hsa_circ_236321,RMVar_hsa_circ_373432,RMVar_hsa_circ_84304,RMVar_hsa_circ_236324,RMVar_hsa_circ_345385,RMVar_hsa_circ_294856 62968 RMVar_ID_62968 Human_SNP_ID_262500252 m1A Human chr5 + 175526721 175526721 175526721 GAGCCATCCTGAATTGCGACGCGTGTACTTCAATAAGGGATTGTAAAGCAGGGAGGAAACCTCTG GAGCCATCCTGAATTGCGACGCGTGTACTTCACTAAGGGATTGTAAAGCAGGGAGGAAACCTCTG A C SFXN1 Ensembl:ENSG00000164466 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:175526671..175526750 26863196 MeRIP-seq:(Medium) rs778475439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76519,Human_RBP_ID_638100,Human_RBP_ID_1040683,Human_RBP_ID_1650797,Human_RBP_ID_1992520,Human_RBP_ID_4852926,Human_RBP_ID_8888178,Human_RBP_ID_15387270,Human_RBP_ID_17529136,Human_RBP_ID_18044937,Human_RBP_ID_18356749,Human_RBP_ID_18838626,Human_RBP_ID_23042726,Human_RBP_ID_24097656,Human_RBP_ID_26524754,Human_RBP_ID_27738653 Human_Splice_Rec_721992,Human_Splice_Rec_722066 Human_miRNA_ID_445504,Human_miRNA_ID_2141982,Human_miRNA_ID_3045788 RMVar_hsa_circ_86081,RMVar_hsa_circ_236321,RMVar_hsa_circ_84304,RMVar_hsa_circ_236324,RMVar_hsa_circ_114506,RMVar_hsa_circ_126968,RMVar_hsa_circ_236325,RMVar_hsa_circ_76191,RMVar_hsa_circ_236326,RMVar_hsa_circ_236327 62969 RMVar_ID_62969 Human_SNP_ID_262500253 m1A Human chr5 + 175526721 175526721 175526721 GAGCCATCCTGAATTGCGACGCGTGTACTTCAATAAGGGATTGTAAAGCAGGGAGGAAACCTCTG GAGCCATCCTGAATTGCGACGCGTGTACTTCAGTAAGGGATTGTAAAGCAGGGAGGAAACCTCTG A G SFXN1 Ensembl:ENSG00000164466 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:175526671..175526750 26863196 MeRIP-seq:(Medium) rs778475439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76519,Human_RBP_ID_638100,Human_RBP_ID_1040683,Human_RBP_ID_1650797,Human_RBP_ID_1992520,Human_RBP_ID_4852926,Human_RBP_ID_8888178,Human_RBP_ID_15387270,Human_RBP_ID_17529136,Human_RBP_ID_18044937,Human_RBP_ID_18356749,Human_RBP_ID_18838626,Human_RBP_ID_23042726,Human_RBP_ID_24097656,Human_RBP_ID_26524754,Human_RBP_ID_27738653 Human_Splice_Rec_721992,Human_Splice_Rec_722066 Human_miRNA_ID_445504,Human_miRNA_ID_2141982,Human_miRNA_ID_3045788 RMVar_hsa_circ_86081,RMVar_hsa_circ_236321,RMVar_hsa_circ_84304,RMVar_hsa_circ_236324,RMVar_hsa_circ_114506,RMVar_hsa_circ_126968,RMVar_hsa_circ_236325,RMVar_hsa_circ_76191,RMVar_hsa_circ_236326,RMVar_hsa_circ_236327 62970 RMVar_ID_62970 Human_SNP_ID_262605527 m1A Human chr5 - 175960125 175960125 175960125 GGTTTCTCTCTATTGTTTTCTGTAGGGGACAAACTATGGGAGGTACAGTGTGAGTCTCCGACCTT GGTTTCTCTCTATTGTTTTCTGTAGGGGACAAGCTATGGGAGGTACAGTGTGAGTCTCCGACCTT T C THOC3 Ensembl:ENSG00000051596 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:175960076..175960125 32194978 MeRIP-seq:(Medium) rs1242877921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354554,Human_RBP_ID_24097908 Human_Splice_Rec_722154,Human_Splice_Rec_722162,Human_Splice_Rec_722164,Human_Splice_Rec_722170 62971 RMVar_ID_62971 Human_SNP_ID_262607699 m1A Human chr5 - 175968073 175968073 175968073 TGCTTGGGATGCAGGAGCTGTTCCGGGGCCACAGCAAGACGCGCGAGTTCCTGGCGCACAGCGCC TGCTTGGGATGCAGGAGCTGTTCCGGGGCCACGGCAAGACGCGCGAGTTCCTGGCGCACAGCGCC T C THOC3 Ensembl:ENSG00000051596 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:175968025..175968165 26863196 MeRIP-seq:(Medium) rs765554994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846885 62972 RMVar_ID_62972 Human_SNP_ID_262675507 m1A Human chr5 - 176238519 176238519 176238519 TCTCAGAGCCGCTGTCGTCCGAGATCACGATGAAATCCTCCATGGCTGCGGGCCCCGACCGAAGA TCTCAGAGCCGCTGTCGTCCGAGATCACGATGTAATCCTCCATGGCTGCGGGCCCCGACCGAAGA T A RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:176238487..176238600;chr5:176238480..176238584 26863196 MeRIP-seq:(Medium) rs866802577 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 62973 RMVar_ID_62973 Human_SNP_ID_262688749 m1A Human chr5 + 176290174 176290174 176290174 ATGCCCACAGCAAGATGTATCTCGCCCACCACAGGCCTTGCCGTGCCCCCTGCGACCTTTGCCAT ATGCCCACAGCAAGATGTATCTCGCCCACCACGGGCCTTGCCGTGCCCCCTGCGACCTTTGCCAT A G SIMC1 Ensembl:ENSG00000170085 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176290123..176290323 26863196 MeRIP-seq:(Medium) rs1390464575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17415446,Human_RBP_ID_26827657 RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_314884,RMVar_hsa_circ_270389,RMVar_hsa_circ_236343,RMVar_hsa_circ_236344,RMVar_hsa_circ_236342 62974 RMVar_ID_62974 Human_SNP_ID_262688829 m1A Human chr5 - 176290310 176290307 176290311 TGCCGAGGGCATGGCACTTCTTGAGGTGGGTGAGTTAGAGCTGGTAGTTGGCACTGCATGGTTTG TGCCGAGGGCATGGCACTTCTTGAGGTGGGT____TAGAGCTGGTAGTTGGCACTGCATGGTTTG AACTC A RF00017-049,lnc-KIAA1191-1 RNACentral:URS000096B6E3,RNACentral:URS0000D5918A SRP RNA,lincRNA intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:176290217..176290336 26863196 MeRIP-seq:(Medium) rs1316282301 Functional Loss DEL dbSNP153 32..35 33 - - - 62975 RMVar_ID_62975 Human_SNP_ID_262703395 m1A Human chr5 - 176347649 176347649 176347649 GATGGAAGGAAAGAAACAGCCACCACGGGCCCATAACCTCAAACCCCGTGACCTGAATGTGCTCA GATGGAAGGAAAGAAACAGCCACCACGGGCCCGTAACCTCAAACCCCGTGACCTGAATGTGCTCA T C KIAA1191 Ensembl:ENSG00000122203 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176347601..176347810 26863196 MeRIP-seq:(Medium) rs766556830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1391031,Human_RBP_ID_5427139,Human_RBP_ID_9398690,Human_RBP_ID_18045057,Human_RBP_ID_27567430 Human_miRNA_ID_2095110,Human_miRNA_ID_2514227 RMVar_hsa_circ_113477,RMVar_hsa_circ_236354,RMVar_hsa_circ_89766,RMVar_hsa_circ_236353 62976 RMVar_ID_62976 Human_SNP_ID_262703396 m1A Human chr5 - 176347649 176347649 176347649 GATGGAAGGAAAGAAACAGCCACCACGGGCCCATAACCTCAAACCCCGTGACCTGAATGTGCTCA GATGGAAGGAAAGAAACAGCCACCACGGGCCCCTAACCTCAAACCCCGTGACCTGAATGTGCTCA T G KIAA1191 Ensembl:ENSG00000122203 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176347601..176347810 26863196 MeRIP-seq:(Medium) rs766556830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1391031,Human_RBP_ID_5427139,Human_RBP_ID_9398690,Human_RBP_ID_18045057,Human_RBP_ID_27567430 Human_miRNA_ID_2095110,Human_miRNA_ID_2514227 RMVar_hsa_circ_113477,RMVar_hsa_circ_236354,RMVar_hsa_circ_89766,RMVar_hsa_circ_236353 62977 RMVar_ID_62977 Human_SNP_ID_262703603 m1A Human chr5 - 176348284 176348284 176348284 GGCAGCCTGCATCAGCCCAGTCCACCCCAAGCACCACTCCGCACTCTTCACCTAAGCAGAGGCCC GGCAGCCTGCATCAGCCCAGTCCACCCCAAGCGCCACTCCGCACTCTTCACCTAAGCAGAGGCCC T C KIAA1191 Ensembl:ENSG00000122203 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176347986..176349033 26863196 MeRIP-seq:(Medium) rs948660738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638250,Human_RBP_ID_1040714,Human_RBP_ID_1320798,Human_RBP_ID_7419305,Human_RBP_ID_17299620,Human_RBP_ID_17413043,Human_RBP_ID_17529195,Human_RBP_ID_18195162,Human_RBP_ID_19016134,Human_RBP_ID_24386809,Human_RBP_ID_26827662 Human_Splice_Rec_722856,Human_Splice_Rec_722857,Human_Splice_Rec_722872,Human_Splice_Rec_722873,Human_Splice_Rec_722886,Human_Splice_Rec_722887,Human_Splice_Rec_722898,Human_Splice_Rec_722899,Human_Splice_Rec_722908,Human_Splice_Rec_722909,Human_Splice_Rec_722922,Human_Splice_Rec_722923,Human_Splice_Rec_722932,Human_Splice_Rec_722933 RMVar_hsa_circ_59628,RMVar_hsa_circ_113477,RMVar_hsa_circ_236354,RMVar_hsa_circ_89766,RMVar_hsa_circ_236353,RMVar_hsa_circ_236356,RMVar_hsa_circ_96878 62978 RMVar_ID_62978 Human_SNP_ID_262706826 m1A Human chr5 - 176361713 176361713 176361713 TCTTGGGGACCTTCGAAATCGCCGCCGCTCTCACAATGGCTTGGGTCCAGACTGCGCCACAGCCT TCTTGGGGACCTTCGAAATCGCCGCCGCTCTCTCAATGGCTTGGGTCCAGACTGCGCCACAGCCT T A KIAA1191 Ensembl:ENSG00000122203 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176361601..176361775 26863196 MeRIP-seq:(Medium) rs561014308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250045,Human_RBP_ID_638257,Human_RBP_ID_1040716,Human_RBP_ID_1650912,Human_RBP_ID_4846169,Human_RBP_ID_5476527,Human_RBP_ID_5509313,Human_RBP_ID_9174819,Human_RBP_ID_18838783,Human_RBP_ID_22459883,Human_RBP_ID_23120209,Human_RBP_ID_27514085 RMVar_hsa_circ_236358,RMVar_hsa_circ_112696 62979 RMVar_ID_62979 Human_SNP_ID_262712150 m1A Human chr5 + 176381843 176381843 176381843 CTAATGAAGATCTGTCTGAGTCTAATGAATATATTGTACAATTTTTAAAGTCCCCAGTTGTGGGA CTAATGAAGATCTGTCTGAGTCTAATGAATATCTTGTACAATTTTTAAAGTCCCCAGTTGTGGGA A C ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35069679 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7689,GWAS_ID_7690,GWAS_ID_7691,GWAS_ID_7692,GWAS_ID_7693,GWAS_ID_7694,GWAS_ID_7695,GWAS_ID_7696,GWAS_ID_7697,GWAS_ID_7698,GWAS_ID_7699,GWAS_ID_7700,GWAS_ID_7701,GWAS_ID_7702,GWAS_ID_7703 62980 RMVar_ID_62980 Human_SNP_ID_262712727 m1A Human chr5 - 176384170 176384170 176384170 GAGGCGTCCCCCGGACCAGTGAAGCTGGAGCCAGGGTGTAAGGCAAGGAGGTGCTGTGTGGCTCC GAGGCGTCCCCCGGACCAGTGAAGCTGGAGCCGGGGTGTAAGGCAAGGAGGTGCTGTGTGGCTCC T C NOP16 Ensembl:ENSG00000048162 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176383986..176384234 32194978 MeRIP-seq:(Medium) rs773186901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638368,Human_RBP_ID_838814,Human_RBP_ID_17663028,Human_RBP_ID_18045084,Human_RBP_ID_18170525,Human_RBP_ID_19015298,Human_RBP_ID_21900859 Human_miRNA_ID_77346,Human_miRNA_ID_80515,Human_miRNA_ID_337893 62981 RMVar_ID_62981 Human_SNP_ID_262712805 m1A Human chr5 - 176384343 176384343 176384343 GGCCATGGCCCGTGATGAGAAGAATTACTATCAAGATACCCCAAAACAGATTCGGAGTAAGATCA GGCCATGGCCCGTGATGAGAAGAATTACTATCCAGATACCCCAAAACAGATTCGGAGTAAGATCA T G NOP16 Ensembl:ENSG00000048162 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176384298..176384403 26863196 MeRIP-seq:(Medium) rs11556383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638371,Human_RBP_ID_943561,Human_RBP_ID_1040722,Human_RBP_ID_1650925,Human_RBP_ID_1992639,Human_RBP_ID_2919094,Human_RBP_ID_18045086,Human_RBP_ID_22681002,Human_RBP_ID_27738746 Human_Splice_Rec_723000,Human_Splice_Rec_723032,Human_Splice_Rec_723038 62982 RMVar_ID_62982 Human_SNP_ID_262713063 m1A Human chr5 - 176385243 176385243 176385243 GGACCTCATTGACTATGTACGCTACATGGTAGAGAACCACGGGGAGGACTATAAGGTGAGCGGCT GGACCTCATTGACTATGTACGCTACATGGTAGGGAACCACGGGGAGGACTATAAGGTGAGCGGCT T C NOP16 Ensembl:ENSG00000048162 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:176385241..176385954 32194978 MeRIP-seq:(Medium) rs757323676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838931,Human_RBP_ID_1650926,Human_RBP_ID_7419427 Human_Splice_Rec_722990,Human_Splice_Rec_722991,Human_Splice_Rec_722998,Human_Splice_Rec_722999,Human_Splice_Rec_723006,Human_Splice_Rec_723007,Human_Splice_Rec_723016,Human_Splice_Rec_723017,Human_Splice_Rec_723024,Human_Splice_Rec_723025,Human_Splice_Rec_723030,Human_Splice_Rec_723031,Human_Splice_Rec_723036,Human_Splice_Rec_723037,Human_Splice_Rec_723044 RMVar_hsa_circ_236364,RMVar_hsa_circ_355909 62983 RMVar_ID_62983 Human_SNP_ID_262713930 m1A Human chr5 - 176388545 176388545 176388545 GGCAGCGTGTTTGAGCTGCTGGTGCGGTGGTCAGCGCGATGCCCAAGGCCAAGGGCAAAACCCGG GGCAGCGTGTTTGAGCTGCTGGTGCGGTGGTCCGCGCGATGCCCAAGGCCAAGGGCAAAACCCGG T G NOP16 Ensembl:ENSG00000048162 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176388301..176388600 26863196 MeRIP-seq:(Medium) rs1165596422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77453,Human_RBP_ID_250588,Human_RBP_ID_789062,Human_RBP_ID_1650934,Human_RBP_ID_4846171,Human_RBP_ID_22459035,Human_RBP_ID_23214377,Human_RBP_ID_26351778,Human_RBP_ID_27842125 62984 RMVar_ID_62984 Human_SNP_ID_262714088 m1A Human chr5 + 176388818 176388818 176388818 AGTCCCGATTTTCTCCTGCTGCTGTGGCCCGGACATGGCGACTCCCGGCCCTGTGATTCCGGAGG AGTCCCGATTTTCTCCTGCTGCTGTGGCCCGGCCATGGCGACTCCCGGCCCTGTGATTCCGGAGG A C ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:176388726..176388984;chr5:176388751..176388977;chr5:176388751..176389003 26863196 MeRIP-seq:(Medium) rs750360319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250207,Human_RBP_ID_638378,Human_RBP_ID_788082,Human_RBP_ID_840028,Human_RBP_ID_1650936,Human_RBP_ID_4823408,Human_RBP_ID_5476534,Human_RBP_ID_8888234,Human_RBP_ID_17662786,Human_RBP_ID_18195165,Human_RBP_ID_18425329,Human_RBP_ID_22459036,Human_RBP_ID_26826844,Human_RBP_ID_27078445,Human_RBP_ID_27334573 Human_miRNA_ID_2572573 RMVar_hsa_circ_124328,RMVar_hsa_circ_125841,RMVar_hsa_circ_236366,RMVar_hsa_circ_236367 62985 RMVar_ID_62985 Human_SNP_ID_262714131 m1A Human chr5 + 176388915 176388915 176388915 GAGGGGCTGAGCCCCACTGTTTACAGGAATCCAGAGAGTTTCAAGGAAAAGTTCGTTCGCAAGAC GAGGGGCTGAGCCCCACTGTTTACAGGAATCCGGAGAGTTTCAAGGAAAAGTTCGTTCGCAAGAC A G ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176388751..176388993 26863196 MeRIP-seq:(Medium) rs1267226794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283999,Human_RBP_ID_638378,Human_RBP_ID_1650936,Human_RBP_ID_1992642,Human_RBP_ID_3967608,Human_RBP_ID_17415455,Human_RBP_ID_18195166,Human_RBP_ID_23214378 Human_Splice_Rec_723053 RMVar_hsa_circ_124328,RMVar_hsa_circ_125841,RMVar_hsa_circ_236366,RMVar_hsa_circ_236367 62986 RMVar_ID_62986 Human_SNP_ID_262714135 m1A Human chr5 + 176388929 176388929 176388929 CACTGTTTACAGGAATCCAGAGAGTTTCAAGGAAAAGTTCGTTCGCAAGACCCGCGAGAACCCGG CACTGTTTACAGGAATCCAGAGAGTTTCAAGGCAAAGTTCGTTCGCAAGACCCGCGAGAACCCGG A C ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:176388776..176389475 26863196 MeRIP-seq:(Medium) rs1438661400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283999,Human_RBP_ID_1650936,Human_RBP_ID_1992642,Human_RBP_ID_3967608,Human_RBP_ID_24098107,Human_RBP_ID_26827670,Human_RBP_ID_27334574 Human_Splice_Rec_723053 Human_miRNA_ID_2610947 RMVar_hsa_circ_124328,RMVar_hsa_circ_125841,RMVar_hsa_circ_236366,RMVar_hsa_circ_236367 62987 RMVar_ID_62987 Human_SNP_ID_262714324 m1A Human chr5 + 176389390 176389390 176389390 CCTACGGCCTCTACTCCTTCCACCGGGGCAACAGCCAGCGCTCTCAGCTCATGATGCGCACCCGG CCTACGGCCTCTACTCCTTCCACCGGGGCAACGGCCAGCGCTCTCAGCTCATGATGCGCACCCGG A G ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:176389326..176389450 32194978 MeRIP-seq:(Medium) rs1295756513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638386,Human_RBP_ID_788084,Human_RBP_ID_9335458,Human_RBP_ID_17415456,Human_RBP_ID_26826848,Human_RBP_ID_27514132 Human_Splice_Rec_723054 Human_miRNA_ID_2330884,Human_miRNA_ID_2893747,Human_miRNA_ID_2963967 RMVar_hsa_circ_125841,RMVar_hsa_circ_236367,RMVar_hsa_circ_75961,RMVar_hsa_circ_236368 62988 RMVar_ID_62988 Human_SNP_ID_262714328 m1A Human chr5 + 176389394 176389394 176389394 CGGCCTCTACTCCTTCCACCGGGGCAACAGCCAGCGCTCTCAGCTCATGATGCGCACCCGGATCG CGGCCTCTACTCCTTCCACCGGGGCAACAGCCCGCGCTCTCAGCTCATGATGCGCACCCGGATCG A C ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176389293..176389498 26863196 MeRIP-seq:(Medium) rs1472015198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638386,Human_RBP_ID_788084,Human_RBP_ID_9335458,Human_RBP_ID_17415456,Human_RBP_ID_21151304,Human_RBP_ID_26826848 Human_Splice_Rec_723054 Human_miRNA_ID_2330884,Human_miRNA_ID_2893747,Human_miRNA_ID_2963967 RMVar_hsa_circ_125841,RMVar_hsa_circ_236367,RMVar_hsa_circ_75961,RMVar_hsa_circ_236368 62989 RMVar_ID_62989 Human_SNP_ID_262714343 m1A Human chr5 + 176389417 176389417 176389417 GCAACAGCCAGCGCTCTCAGCTCATGATGCGCACCCGGATCGCCGCCCAGGGTTTCACGGTCGCA GCAACAGCCAGCGCTCTCAGCTCATGATGCGCGCCCGGATCGCCGCCCAGGGTTTCACGGTCGCA A G ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:176389401..176389425 26863196 MeRIP-seq:(Medium) rs1177554188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638386,Human_RBP_ID_1650942,Human_RBP_ID_8610912,Human_RBP_ID_9335458,Human_RBP_ID_17415456,Human_RBP_ID_24098110,Human_RBP_ID_26826850 Human_Splice_Rec_723054 RMVar_hsa_circ_125841,RMVar_hsa_circ_236367,RMVar_hsa_circ_75961,RMVar_hsa_circ_236368 62990 RMVar_ID_62990 Human_SNP_ID_262715136 m1A Human chr5 - 176392620 176392620 176392620 TCTCCAGGCGCTGGGAGGGGGGCCCTCACCCCATCACGCCTCGCTCCCTCCTGGCCCTCTGGTCC TCTCCAGGCGCTGGGAGGGGGGCCCTCACCCCGTCACGCCTCGCTCCCTCCTGGCCCTCTGGTCC T C CLTB Ensembl:ENSG00000175416 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs5866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76846,Human_RBP_ID_17663033,Human_RBP_ID_26524920,Human_RBP_ID_26826851 GWAS_ID_7704,GWAS_ID_7705,GWAS_ID_7706,GWAS_ID_7707,GWAS_ID_7708,GWAS_ID_7709,GWAS_ID_7710,GWAS_ID_7711,GWAS_ID_7712,GWAS_ID_7713,GWAS_ID_7714,GWAS_ID_7715,GWAS_ID_7716,GWAS_ID_7717,GWAS_ID_7718 RMVar_hsa_circ_86885,RMVar_hsa_circ_236369 62991 RMVar_ID_62991 Human_SNP_ID_262715222 m1A Human chr5 - 176392892 176392892 176392892 GAAGGAATCCAAGGAGGAGACCCCAGGCACAGAGTGGGAGAAGGTGGCCCAGCTATGTGACTTCA GAAGGAATCCAAGGAGGAGACCCCAGGCACAGGGTGGGAGAAGGTGGCCCAGCTATGTGACTTCA T C CLTB Ensembl:ENSG00000175416 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:176392876..176392900 26863196 MeRIP-seq:(Medium) rs756695540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27078464 Human_Splice_Rec_723064,Human_Splice_Rec_723072,Human_Splice_Rec_723086,Human_Splice_Rec_723090 Human_miRNA_ID_343169,Human_miRNA_ID_1337511,Human_miRNA_ID_2867524 RMVar_hsa_circ_86885,RMVar_hsa_circ_236369 62992 RMVar_ID_62992 Human_SNP_ID_262715223 m1A Human chr5 - 176392892 176392892 176392892 GAAGGAATCCAAGGAGGAGACCCCAGGCACAGAGTGGGAGAAGGTGGCCCAGCTATGTGACTTCA GAAGGAATCCAAGGAGGAGACCCCAGGCACAGCGTGGGAGAAGGTGGCCCAGCTATGTGACTTCA T G CLTB Ensembl:ENSG00000175416 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:176392876..176392900 26863196 MeRIP-seq:(Medium) rs756695540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27078464 Human_Splice_Rec_723064,Human_Splice_Rec_723072,Human_Splice_Rec_723086,Human_Splice_Rec_723090 Human_miRNA_ID_343169,Human_miRNA_ID_1337511,Human_miRNA_ID_2867524 RMVar_hsa_circ_86885,RMVar_hsa_circ_236369 62993 RMVar_ID_62993 Human_SNP_ID_262717413 m1A Human chr5 + 176400618 176400618 176400618 GCCACACCCGCTCTGGCACCCACGCCCTCCGCATTCCTGTCTGCAGGCATCCCACTCCAGCTACC GCCACACCCGCTCTGGCACCCACGCCCTCCGCCTTCCTGTCTGCAGGCATCCCACTCCAGCTACC A C ARL10 Ensembl:ENSG00000175414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176400616..176400730 26863196 MeRIP-seq:(Medium) rs1435290630 Functional Loss SNV dbSNP153 33..33 33 - - - 62994 RMVar_ID_62994 Human_SNP_ID_262717414 m1A Human chr5 + 176400618 176400618 176400618 GCCACACCCGCTCTGGCACCCACGCCCTCCGCATTCCTGTCTGCAGGCATCCCACTCCAGCTACC GCCACACCCGCTCTGGCACCCACGCCCTCCGCGTTCCTGTCTGCAGGCATCCCACTCCAGCTACC A G ARL10 Ensembl:ENSG00000175414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176400616..176400730 26863196 MeRIP-seq:(Medium) rs1435290630 Functional Loss SNV dbSNP153 33..33 33 - - - 62995 RMVar_ID_62995 Human_SNP_ID_262717691 m1A Human chr5 - 176401808 176401808 176401808 CACGGGGGATGGGAAGGAAGGAGAAATCAAGGACGAACAGGAGGCTGGGGCCTCAGCACCCTCGG CACGGGGGATGGGAAGGAAGGAGAAATCAAGGGCGAACAGGAGGCTGGGGCCTCAGCACCCTCGG T C CLTB Ensembl:ENSG00000175416 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176401801..176401940 26863196 MeRIP-seq:(Medium) rs1182589491 Functional Loss SNV dbSNP153 33..33 33 - - - 62996 RMVar_ID_62996 Human_SNP_ID_262721291 m1A Human chr5 + 176416322 176416322 176416322 GCCGCCGGGTCCTCCTCCGCCGCCTCCGGGGCACCGCTCTCCGACGACGAGAAGAAGCCAAAGTC GCCGCCGGGTCCTCCTCCGCCGCCTCCGGGGCCCCGCTCTCCGACGACGAGAAGAAGCCAAAGTC A C RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:176416275..176416447 26863196 MeRIP-seq:(Medium) rs145048156 Functional Loss SNV dbSNP153 33..33 33 - - - 62997 RMVar_ID_62997 Human_SNP_ID_262721303 m1A Human chr5 + 176416344 176416344 176416344 CCTCCGGGGCACCGCTCTCCGACGACGAGAAGAAGCCAAAGTCATCAGCCATTTTCCCCGCGCCT CCTCCGGGGCACCGCTCTCCGACGACGAGAAGCAGCCAAAGTCATCAGCCATTTTCCCCGCGCCT A C RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:176416148..176416575 26863196 MeRIP-seq:(Medium) rs1333797276 Functional Loss SNV dbSNP153 33..33 33 - - - 62998 RMVar_ID_62998 Human_SNP_ID_262721373 m1A Human chr5 - 176416509 176416509 176416509 GCAGTGACAGCCAGCCGGGCCCGGTGGCGGAGAGGAAGTGCGGTCCGCGCCAAGCCCGTCCCCGC GCAGTGACAGCCAGCCGGGCCCGGTGGCGGAGGGGAAGTGCGGTCCGCGCCAAGCCCGTCCCCGC T C CLTB Ensembl:ENSG00000175416 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:176416411..176416508 26863410 MeRIP-seq:(Medium) rs1450244683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4823477,Human_RBP_ID_5151371 62999 RMVar_ID_62999 Human_SNP_ID_262729574 m1A Human chr5 + 176448421 176448421 176448421 GCGTAGAGGCGGCGGCAAAATGGCGGCGCCTGAGGAGCGGGATCTAACCCAGGAGCAGACAGAGA GCGTAGAGGCGGCGGCAAAATGGCGGCGCCTGCGGAGCGGGATCTAACCCAGGAGCAGACAGAGA A C FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176448351..176453176 26863196 MeRIP-seq:(Medium) rs907645195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_787591,Human_RBP_ID_839932,Human_RBP_ID_1992651,Human_RBP_ID_4846177,Human_RBP_ID_5326947,Human_RBP_ID_7419459,Human_RBP_ID_18425052,Human_RBP_ID_19124960,Human_RBP_ID_23050189 Human_Splice_Rec_723099,Human_Splice_Rec_723117 RMVar_hsa_circ_110296,RMVar_hsa_circ_236370 63000 RMVar_ID_63000 Human_SNP_ID_262737926 m1A Human chr5 - 176479245 176479245 176479245 TCAGAACACATCCTATTATACCTCTATGTTCCAGTTATGCTGTTCCAAGGTATGGCGACACTGAT TCAGAACACATCCTATTATACCTCTATGTTCCGGTTATGCTGTTCCAAGGTATGGCGACACTGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176479132..176479250 26863196 MeRIP-seq:(Medium) rs199533667 Functional Loss SNV dbSNP153 33..33 33 - - - 63001 RMVar_ID_63001 Human_SNP_ID_262750463 m1A Human chr5 + 176527094 176527094 176527094 CTACATATATATGTAATTTTATATATATATAAAACCTTTCTAACACAGAACACAGGCGCTGGGCC CTACATATATATGTAATTTTATATATATATAATACCTTTCTAACACAGAACACAGGCGCTGGGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176527043..176527144 32194978 MeRIP-seq:(Medium) rs776355644 Functional Loss SNV dbSNP153 33..33 33 - - - 63002 RMVar_ID_63002 Human_SNP_ID_262750761 m1A Human chr5 + 176528019 176528019 176528019 TGTGCAGTACAGTGCATGGCAGTTATCAGCTGAGCACAGACCCCCAACCCTGCCCCACGACCGCC TGTGCAGTACAGTGCATGGCAGTTATCAGCTGGGCACAGACCCCCAACCCTGCCCCACGACCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176527968..176528056 26863196 MeRIP-seq:(Medium) rs1203432322 Functional Loss SNV dbSNP153 33..33 33 - - - 63003 RMVar_ID_63003 Human_SNP_ID_262751967 m1A Human chr5 + 176530637 176530637 176530637 GCAGCGGATCGTGGGGCAGGTAGTGCAGGGGCACCGACGGGGAAAGGGCTGGGCCAGGCGCAGAG GCAGCGGATCGTGGGGCAGGTAGTGCAGGGGCGCCGACGGGGAAAGGGCTGGGCCAGGCGCAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176530587..176530675 26863196 MeRIP-seq:(Medium) rs573854860 Functional Loss SNV dbSNP153 33..33 33 - - - 63004 RMVar_ID_63004 Human_SNP_ID_262752162 m1A Human chr5 - 176531014 176531014 176531014 AGCCCCCTGCCCCCTCTCTTGGCAGCTTATCCAGGCGTGCACCATGCAGCAGCTGCCTGTGCCCT AGCCCCCTGCCCCCTCTCTTGGCAGCTTATCCGGGCGTGCACCATGCAGCAGCTGCCTGTGCCCT T C RNF44 Ensembl:ENSG00000146083 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176530965..176531032 26863196 MeRIP-seq:(Medium) rs1333352410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638549,Human_RBP_ID_3967610,Human_RBP_ID_5134060,Human_RBP_ID_18045192,Human_RBP_ID_24098288,Human_RBP_ID_26826857 Human_Splice_Rec_723144,Human_Splice_Rec_723172,Human_Splice_Rec_723198 RMVar_hsa_circ_75927,RMVar_hsa_circ_236381 63005 RMVar_ID_63005 Human_SNP_ID_262752342 m1A Human chr5 + 176531524 176531524 176531524 GCTGCCCACTGAACATCACGGAGCATGCTGGGAGCTGCTGGGCACTGCAGCCAGGGATGTGCTGG GCTGCCCACTGAACATCACGGAGCATGCTGGGCGCTGCTGGGCACTGCAGCCAGGGATGTGCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176531473..176531538 26863196 MeRIP-seq:(Medium) rs767518967 Functional Loss SNV dbSNP153 33..33 33 - - - 63006 RMVar_ID_63006 Human_SNP_ID_262752364 m1A Human chr5 - 176531582 176531582 176531582 TCCCTCTGTCCTACACGGTCACCACAGTGACGACCCAAGGCTTCCCCTTGCCTACAGGCCAGCAC TCCCTCTGTCCTACACGGTCACCACAGTGACGCCCCAAGGCTTCCCCTTGCCTACAGGCCAGCAC T G RNF44 Ensembl:ENSG00000146083 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176530646..176531890 32194978 MeRIP-seq:(Medium) rs553268338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638554,Human_RBP_ID_943160 Human_Splice_Rec_723142,Human_Splice_Rec_723170,Human_Splice_Rec_723196 63007 RMVar_ID_63007 Human_SNP_ID_262752732 m1A Human chr5 + 176532406 176532406 176532406 GAGCTGGCCCGGGGTGCTGCCAGGTCCCGCAGAGAATCGCCGCTGGCCCACGGGGGCGGAGGGTG GAGCTGGCCCGGGGTGCTGCCAGGTCCCGCAGCGAATCGCCGCTGGCCCACGGGGGCGGAGGGTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:176532376..176532425 26863196 MeRIP-seq:(Medium) rs1369946786 Functional Loss SNV dbSNP153 33..33 33 - - - 63008 RMVar_ID_63008 Human_SNP_ID_262752752 m1A Human chr5 - 176532437 176532437 176532437 CGACCATGGGCTCTGGCAGTGACTAGGTGGCCACCCTCCGCCCCCGTGGGCCAGCGGCGATTCTC CGACCATGGGCTCTGGCAGTGACTAGGTGGCCCCCCTCCGCCCCCGTGGGCCAGCGGCGATTCTC T G RNF44 Ensembl:ENSG00000146083 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr5:176531988..176532525;chr5:176532321..176532535 26863196 MeRIP-seq:(Medium) rs1266578738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_649380,Human_RBP_ID_4845500 Human_Splice_Rec_723138,Human_Splice_Rec_723139,Human_Splice_Rec_723166,Human_Splice_Rec_723167,Human_Splice_Rec_723192,Human_Splice_Rec_723193,Human_Splice_Rec_723200,Human_Splice_Rec_723202 63009 RMVar_ID_63009 Human_SNP_ID_262755200 m1A Human chr5 - 176540006 176540006 176540006 TCCTGTAAAAGGTGAGTTAGGAACAGAGCTTCAAACCGCCGAAAAGTGAAATGGATTGGCAGAAA TCCTGTAAAAGGTGAGTTAGGAACAGAGCTTCGAACCGCCGAAAAGTGAAATGGATTGGCAGAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176539872..176540033 26863196 MeRIP-seq:(Medium) rs924568977 Functional Loss SNV dbSNP153 33..33 33 - - - 63010 RMVar_ID_63010 Human_SNP_ID_262756126 m1A Human chr5 - 176543436 176543436 176543436 CGGGGCCGGGGCGGGGGTCCTGGAAGCTGCGCAGCCGGTGTGGGCCCCGCGCGCCCGGGTGGTGA CGGGGCCGGGGCGGGGGTCCTGGAAGCTGCGCCGCCGGTGTGGGCCCCGCGCGCCCGGGTGGTGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:176543293..176543460;chr5:176543297..176543460 26863196 MeRIP-seq:(Medium) rs910989707 Functional Loss SNV dbSNP153 33..33 33 - - - 63011 RMVar_ID_63011 Human_SNP_ID_262771860 m1A Human chr5 + 176596325 176596325 176596325 CTCGTTCTACCTCACGTGCTGCCCGAGACCTCACATTCAGAGACGTGCCCACTCGCGGGTCTCAC CTCGTTCTACCTCACGTGCTGCCCGAGACCTCGCATTCAGAGACGTGCCCACTCGCGGGTCTCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176596229..176596437 26863196 MeRIP-seq:(Medium) rs115870095 Functional Loss SNV dbSNP153 33..33 33 - - - 63012 RMVar_ID_63012 Human_SNP_ID_262772272 m1A Human chr5 - 176597458 176597458 176597458 CAGCGCCCCCGCCGGGGCCGCGGACTCGCGACAACTTCACCAAGGCGCCGTCGTGGGAGGCGAGC CAGCGCCCCCGCCGGGGCCGCGGACTCGCGACGACTTCACCAAGGCGCCGTCGTGGGAGGCGAGC T C GPRIN1 Ensembl:ENSG00000169258 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176597408..176597610 26863196 MeRIP-seq:(Medium) rs1296609137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18045209 RMVar_hsa_circ_122287,RMVar_hsa_circ_236387 63013 RMVar_ID_63013 Human_SNP_ID_262772310 m1A Human chr5 - 176597514 176597514 176597514 CGGCCAGAAAGACCTGGAAGCCGCTGGGGCCGAGAGAAGCCCCTGCCCAGAGGCCGCAGCGCCCC CGGCCAGAAAGACCTGGAAGCCGCTGGGGCCGGGAGAAGCCCCTGCCCAGAGGCCGCAGCGCCCC T C GPRIN1 Ensembl:ENSG00000169258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176597469..176597705 26863196 MeRIP-seq:(Medium) rs1010596410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9307269 RMVar_hsa_circ_122287,RMVar_hsa_circ_236387 63014 RMVar_ID_63014 Human_SNP_ID_262772418 m1A Human chr5 + 176597725 176597725 176597725 ACTCAGGGGGACCACCTTCCCCAAGGATGGGGACTCCGTTTTTCTGGAAGGTGCAGAGTCGGCTT ACTCAGGGGGACCACCTTCCCCAAGGATGGGGCCTCCGTTTTTCTGGAAGGTGCAGAGTCGGCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr5:176597674..176597905;chr5:176597634..176598328 26863196,32194978 MeRIP-seq:(Medium) rs1399997174 Functional Loss SNV dbSNP153 33..33 33 - - - 63015 RMVar_ID_63015 Human_SNP_ID_262775726 m1A Human chr5 - 176610021 176610021 176610021 GGCGGCGGGAGCCGGAGCGCATCTCGCCCAGGAGCCGGAGCAGCGGCACTGCCTGGTAAGCGCCG GGCGGCGGGAGCCGGAGCGCATCTCGCCCAGGTGCCGGAGCAGCGGCACTGCCTGGTAAGCGCCG T A GPRIN1 Ensembl:ENSG00000169258 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:176610016..176610128 26863196 MeRIP-seq:(Medium) rs911221688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846181 Human_Splice_Rec_723403 Human_miRNA_ID_2039232,Human_miRNA_ID_3018212 RMVar_hsa_circ_122287,RMVar_hsa_circ_236387 63016 RMVar_ID_63016 Human_SNP_ID_262786027 m1A Human chr5 - 176647454 176647454 176647454 AGCGCCGGTCGGGCCCCGCCCGCCCCTCAGGGACCGCCCTCAGCATCCAGACCTCCTTGCCCGGA AGCGCCGGTCGGGCCCCGCCCGCCCCTCAGGGCCCGCCCTCAGCATCCAGACCTCCTTGCCCGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:176647418..176647561;chr5:176647446..176647552 26863196 MeRIP-seq:(Medium) rs900876014 Functional Loss SNV dbSNP153 33..33 33 - - - 63017 RMVar_ID_63017 Human_SNP_ID_262855638 m1A Human chr5 - 176907176 176907176 176907176 TAACCTTTTCATCTGTTTTTCTCTGTTACAGGAAAAAGGCCACAGTGAAGGCCGACTCCTTAGTT TAACCTTTTCATCTGTTTTTCTCTGTTACAGGCAAAAGGCCACAGTGAAGGCCGACTCCTTAGTT T G UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:176907126..176907175 32194978 MeRIP-seq:(Medium) rs1332911850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_723848,Human_Splice_Rec_723849,Human_Splice_Rec_723874,Human_Splice_Rec_723875,Human_Splice_Rec_723898,Human_Splice_Rec_723899,Human_Splice_Rec_723926,Human_Splice_Rec_723927,Human_Splice_Rec_723944,Human_Splice_Rec_723945,Human_Splice_Rec_723951 RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_266301,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_236396 63018 RMVar_ID_63018 Human_SNP_ID_262862916 m1A Human chr5 - 176935222 176935222 176935222 ATTCAGTGTAGTTATAGTGTGGGCATTATGAAAGGAAATGGTGGGCAGTTGGAGAATGACAAATG ATTCAGTGTAGTTATAGTGTGGGCATTATGAAGGGAAATGGTGGGCAGTTGGAGAATGACAAATG T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176935216..176935318 26863196 MeRIP-seq:(Medium) rs568290235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15564923 RMVar_hsa_circ_11659,RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_122596,RMVar_hsa_circ_236396,RMVar_hsa_circ_236400,RMVar_hsa_circ_120397,RMVar_hsa_circ_363411,RMVar_hsa_circ_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402 63019 RMVar_ID_63019 Human_SNP_ID_262862917 m1A Human chr5 - 176935224 176935224 176935224 CAATTCAGTGTAGTTATAGTGTGGGCATTATGAAAGGAAATGGTGGGCAGTTGGAGAATGACAAA CAATTCAGTGTAGTTATAGTGTGGGCATTATGGAAGGAAATGGTGGGCAGTTGGAGAATGACAAA T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176935211..176935304 26863196 MeRIP-seq:(Medium) rs1022334632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15564923 RMVar_hsa_circ_11659,RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_122596,RMVar_hsa_circ_236396,RMVar_hsa_circ_236400,RMVar_hsa_circ_120397,RMVar_hsa_circ_363411,RMVar_hsa_circ_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402 63020 RMVar_ID_63020 Human_SNP_ID_262863071 m1A Human chr5 - 176935994 176935994 176935994 TAGGGAGAAATAGATTATAGGAGAGTTAGGGAAGCTGAAGGCATTAACTGTATACACTTTGAGTC TAGGGAGAAATAGATTATAGGAGAGTTAGGGAGGCTGAAGGCATTAACTGTATACACTTTGAGTC T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176935988..176936072 26863196 MeRIP-seq:(Medium) rs1291362656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420012,Human_RBP_ID_10197174,Human_RBP_ID_15392615 RMVar_hsa_circ_11659,RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_122596,RMVar_hsa_circ_236396,RMVar_hsa_circ_236400,RMVar_hsa_circ_120397,RMVar_hsa_circ_363411,RMVar_hsa_circ_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402 63021 RMVar_ID_63021 Human_SNP_ID_262863072 m1A Human chr5 - 176935994 176935994 176935994 TAGGGAGAAATAGATTATAGGAGAGTTAGGGAAGCTGAAGGCATTAACTGTATACACTTTGAGTC TAGGGAGAAATAGATTATAGGAGAGTTAGGGACGCTGAAGGCATTAACTGTATACACTTTGAGTC T G UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176935988..176936072 26863196 MeRIP-seq:(Medium) rs1291362656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420012,Human_RBP_ID_10197174,Human_RBP_ID_15392615 RMVar_hsa_circ_11659,RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_122596,RMVar_hsa_circ_236396,RMVar_hsa_circ_236400,RMVar_hsa_circ_120397,RMVar_hsa_circ_363411,RMVar_hsa_circ_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402 63022 RMVar_ID_63022 Human_SNP_ID_262863224 m1A Human chr5 - 176936713 176936713 176936713 GAAGATTGTGAGGTGGGGAGAGTGCTACAGGTAGAAGGAACAATAAATGCAAAAACCCTGAGGTG GAAGATTGTGAGGTGGGGAGAGTGCTACAGGTGGAAGGAACAATAAATGCAAAAACCCTGAGGTG T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:176936580..176936936 26863196 MeRIP-seq:(Medium) rs1047276397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838707,Human_RBP_ID_7420020,Human_RBP_ID_10236260,Human_RBP_ID_15392654,Human_RBP_ID_23042846 RMVar_hsa_circ_11659,RMVar_hsa_circ_236397,RMVar_hsa_circ_101806,RMVar_hsa_circ_105300,RMVar_hsa_circ_236395,RMVar_hsa_circ_373078,RMVar_hsa_circ_87528,RMVar_hsa_circ_236398,RMVar_hsa_circ_122596,RMVar_hsa_circ_236396,RMVar_hsa_circ_236400,RMVar_hsa_circ_120397,RMVar_hsa_circ_363411,RMVar_hsa_circ_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402 63023 RMVar_ID_63023 Human_SNP_ID_262873096 m1A Human chr5 - 176975422 176975422 176975422 GAAAACGAAGACAAAACAGTCGAATAGAGCAAAGTGTTTGGCCAAAAGAAAAATCGCACGTATGT GAAAACGAAGACAAAACAGTCGAATAGAGCAAGGTGTTTGGCCAAAAGAAAAATCGCACGTATGT T C UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176975354..176975421 26863196 MeRIP-seq:(Medium) rs757253892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73964,Human_RBP_ID_944811,Human_RBP_ID_5610691,Human_RBP_ID_15393745,Human_RBP_ID_24098523,Human_RBP_ID_26352919,Human_RBP_ID_27826124 Human_Splice_Rec_723830,Human_Splice_Rec_723831,Human_Splice_Rec_723856,Human_Splice_Rec_723857,Human_Splice_Rec_723882,Human_Splice_Rec_723883,Human_Splice_Rec_723906,Human_Splice_Rec_723907,Human_Splice_Rec_723970,Human_Splice_Rec_723971,Human_Splice_Rec_723978,Human_Splice_Rec_723979,Human_Splice_Rec_723984,Human_Splice_Rec_723985,Human_Splice_Rec_723992,Human_Splice_Rec_723993,Human_Splice_Rec_723996 Human_miRNA_ID_879139,Human_miRNA_ID_1348605,Human_miRNA_ID_1812145 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_113131,RMVar_hsa_circ_3534,RMVar_hsa_circ_70873,RMVar_hsa_circ_236405,RMVar_hsa_circ_75709,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_328319,RMVar_hsa_circ_8543,RMVar_hsa_circ_311842,RMVar_hsa_circ_366032,RMVar_hsa_circ_288555,RMVar_hsa_circ_236416,RMVar_hsa_circ_64640,RMVar_hsa_circ_294228 63024 RMVar_ID_63024 Human_SNP_ID_262873099 m1A Human chr5 - 176975427 176975427 176975427 TTGCAGAAAACGAAGACAAAACAGTCGAATAGAGCAAAGTGTTTGGCCAAAAGAAAAATCGCACG TTGCAGAAAACGAAGACAAAACAGTCGAATAGGGCAAAGTGTTTGGCCAAAAGAAAAATCGCACG T C UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176975348..176975427 26863196 MeRIP-seq:(Medium) rs1415895770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73964,Human_RBP_ID_944811,Human_RBP_ID_5610691,Human_RBP_ID_15393745,Human_RBP_ID_24098523,Human_RBP_ID_26352919,Human_RBP_ID_27826124 Human_Splice_Rec_723830,Human_Splice_Rec_723831,Human_Splice_Rec_723856,Human_Splice_Rec_723857,Human_Splice_Rec_723882,Human_Splice_Rec_723883,Human_Splice_Rec_723906,Human_Splice_Rec_723907,Human_Splice_Rec_723970,Human_Splice_Rec_723971,Human_Splice_Rec_723978,Human_Splice_Rec_723979,Human_Splice_Rec_723984,Human_Splice_Rec_723985,Human_Splice_Rec_723992,Human_Splice_Rec_723993,Human_Splice_Rec_723996 Human_miRNA_ID_879139,Human_miRNA_ID_1348605,Human_miRNA_ID_1812145 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_113131,RMVar_hsa_circ_3534,RMVar_hsa_circ_70873,RMVar_hsa_circ_236405,RMVar_hsa_circ_75709,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_328319,RMVar_hsa_circ_8543,RMVar_hsa_circ_311842,RMVar_hsa_circ_366032,RMVar_hsa_circ_288555,RMVar_hsa_circ_236416,RMVar_hsa_circ_64640,RMVar_hsa_circ_294228 63025 RMVar_ID_63025 Human_SNP_ID_262874494 m1A Human chr5 - 176980238 176980238 176980238 CAGATGGACAGACGGATGGAATTTATTAGGGGAATTGGCTCATTCAATTATGGAGGTTGAAAAGT CAGATGGACAGACGGATGGAATTTATTAGGGGGATTGGCTCATTCAATTATGGAGGTTGAAAAGT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176980236..176980353 26863196 MeRIP-seq:(Medium) rs938888249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24098530 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_113131,RMVar_hsa_circ_236405,RMVar_hsa_circ_75709,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_328319,RMVar_hsa_circ_311842,RMVar_hsa_circ_366032,RMVar_hsa_circ_288555,RMVar_hsa_circ_236416,RMVar_hsa_circ_64640,RMVar_hsa_circ_294228 63026 RMVar_ID_63026 Human_SNP_ID_262874505 m1A Human chr5 + 176980266 176980266 176980266 CAATTCCCCTAATAAATTCCATCCGTCTGTCCATCTGTCCTTCCATCCATCCACCCTTCTGTCCG CAATTCCCCTAATAAATTCCATCCGTCTGTCCCTCTGTCCTTCCATCCATCCACCCTTCTGTCCG A C RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:176980262..176980392 26863196 MeRIP-seq:(Medium) rs1048399230 Functional Loss SNV dbSNP153 33..33 33 - - - 63027 RMVar_ID_63027 Human_SNP_ID_262875167 m1A Human chr5 - 176982596 176982596 176982596 TCTAGACAAAAGGATGCCACGGAGAAAGAAAAAAGTTAAAGAAGTCTCCGAATCTCGGAACCTGG TCTAGACAAAAGGATGCCACGGAGAAAGAAAAGAGTTAAAGAAGTCTCCGAATCTCGGAACCTGG T C UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176982547..176982679 26863196 MeRIP-seq:(Medium) rs1561878895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943167,Human_RBP_ID_3968425 Human_Splice_Rec_723828,Human_Splice_Rec_723854,Human_Splice_Rec_723880,Human_Splice_Rec_723904,Human_Splice_Rec_723968,Human_Splice_Rec_723976,Human_Splice_Rec_723982,Human_Splice_Rec_723990,Human_Splice_Rec_724000 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_113131,RMVar_hsa_circ_236405,RMVar_hsa_circ_75709,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_328319,RMVar_hsa_circ_311842,RMVar_hsa_circ_366032,RMVar_hsa_circ_288555,RMVar_hsa_circ_236416,RMVar_hsa_circ_64640,RMVar_hsa_circ_294228,RMVar_hsa_circ_236417,RMVar_hsa_circ_376251 63028 RMVar_ID_63028 Human_SNP_ID_262882160 m1A Human chr5 + 177006472 177006472 177006472 TTCGGCAAGGCCAGCCCCGGCGTCCGGAGCCCACCCCCGCGTCGCGAGAGACACACCCCGGCATC TTCGGCAAGGCCAGCCCCGGCGTCCGGAGCCCCCCCCCGCGTCGCGAGAGACACACCCCGGCATC A C RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177006466..177006726 26863196 MeRIP-seq:(Medium) rs1189996052 Functional Loss SNV dbSNP153 33..33 33 - - - 63029 RMVar_ID_63029 Human_SNP_ID_262882191 m1A Human chr5 + 177006571 177006571 177006571 CTTGGCGTCGGGAAGCGCCCCTCCCGGAGAGTAGCGGGCCGCGGACCCGCTGAGGAAGAAAAGGA CTTGGCGTCGGGAAGCGCCCCTCCCGGAGAGTTGCGGGCCGCGGACCCGCTGAGGAAGAAAAGGA A T RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177006569..177006722 26863196 MeRIP-seq:(Medium) rs1014610490 Functional Loss SNV dbSNP153 33..33 33 - - - 63030 RMVar_ID_63030 Human_SNP_ID_262886058 m1A Human chr5 + 177022767 177022766 177022767 GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACA GAAGATGGAGTATCCCGCGCCGGCCACGGTGC_GGCCGCGGACGGCGGAGCGGCCGGGCCTTACA CA C ZNF346 Ensembl:ENSG00000113761 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177022721..177022900 26863196 MeRIP-seq:(Medium) rs1233140989 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_839885,Human_RBP_ID_4846188,Human_RBP_ID_19015310,Human_RBP_ID_22099853 RMVar_hsa_circ_80510,RMVar_hsa_circ_236418 63031 RMVar_ID_63031 Human_SNP_ID_262886059 m1A Human chr5 + 177022767 177022767 177022767 GAAGATGGAGTATCCCGCGCCGGCCACGGTGCAGGCCGCGGACGGCGGAGCGGCCGGGCCTTACA GAAGATGGAGTATCCCGCGCCGGCCACGGTGCCGGCCGCGGACGGCGGAGCGGCCGGGCCTTACA A C ZNF346 Ensembl:ENSG00000113761 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177022721..177022900 26863196 MeRIP-seq:(Medium) rs868024736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839885,Human_RBP_ID_4846188,Human_RBP_ID_19015310,Human_RBP_ID_22099853 RMVar_hsa_circ_80510,RMVar_hsa_circ_236418 63032 RMVar_ID_63032 Human_SNP_ID_262886115 m1A Human chr5 + 177022876 177022876 177022876 TTTGACCGCGAGAGGGCGCGCCGCCTGTGGGAAGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGA TTTGACCGCGAGAGGGCGCGCCGCCTGTGGGACGCCGTGTCCGGTGCCCAGCCGGTGGGTAGAGA A C ZNF346 Ensembl:ENSG00000113761 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:177022773..177022920 26863196 MeRIP-seq:(Medium) rs1460897261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250023,Human_RBP_ID_839886,Human_RBP_ID_944813,Human_RBP_ID_9335826,Human_RBP_ID_18425218 Human_Splice_Rec_724001,Human_Splice_Rec_724007,Human_Splice_Rec_724019,Human_Splice_Rec_724025,Human_Splice_Rec_724035,Human_Splice_Rec_724045,Human_Splice_Rec_724057,Human_Splice_Rec_724065,Human_Splice_Rec_724081 RMVar_hsa_circ_80510,RMVar_hsa_circ_236418 63033 RMVar_ID_63033 Human_SNP_ID_262895615 m1A Human chr5 + 177059884 177059884 177059884 TTACAGTCTAGCAGAGAAGACAGGCATTGAGCAAACAGTTACAACTGTGACAAACTTCAGAAAAA TTACAGTCTAGCAGAGAAGACAGGCATTGAGCCAACAGTTACAACTGTGACAAACTTCAGAAAAA A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177059865..177060085 26863196 MeRIP-seq:(Medium) rs1348652349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236426,RMVar_hsa_circ_21225,RMVar_hsa_circ_19708,RMVar_hsa_circ_307082,RMVar_hsa_circ_236422,RMVar_hsa_circ_91996,RMVar_hsa_circ_236425,RMVar_hsa_circ_277444,RMVar_hsa_circ_236427,RMVar_hsa_circ_236428 63034 RMVar_ID_63034 Human_SNP_ID_262896234 m1A Human chr5 - 177062086 177062086 177062086 TGGTACTGTTCTATGGAGTTCAGCACTATCTTACATGTTTTGCAGGGGTAGCCCTTTCCAGCTGA TGGTACTGTTCTATGGAGTTCAGCACTATCTTGCATGTTTTGCAGGGGTAGCCCTTTCCAGCTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177044454..177064653 32194978 MeRIP-seq:(Medium) rs767285871 Functional Loss SNV dbSNP153 33..33 33 - - - 63035 RMVar_ID_63035 Human_SNP_ID_262903314 m1A Human chr5 + 177089601 177089601 177089601 TCCAGCTTGGGTCCCTGAGAGCTGTGAGAAGGAGATGCGGCTGCTGCTGGCCCTGTTGGGGGTCC TCCAGCTTGGGTCCCTGAGAGCTGTGAGAAGGCGATGCGGCTGCTGCTGGCCCTGTTGGGGGTCC A C FGFR4 Ensembl:ENSG00000160867 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:177089497..177089693;chr5:177089508..177089793;chr5:177089491..177089661 26863196 MeRIP-seq:(Medium) rs1254575384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788821,Human_RBP_ID_1391068,Human_RBP_ID_4845510,Human_RBP_ID_17662794,Human_RBP_ID_24098720 Human_Splice_Rec_724088,Human_Splice_Rec_724089,Human_Splice_Rec_724096,Human_Splice_Rec_724097,Human_Splice_Rec_724130,Human_Splice_Rec_724131,Human_Splice_Rec_724134,Human_Splice_Rec_724135,Human_Splice_Rec_724168,Human_Splice_Rec_724169,Human_Splice_Rec_724204,Human_Splice_Rec_724205,Human_Splice_Rec_724208,Human_Splice_Rec_724209,Human_Splice_Rec_724212,Human_Splice_Rec_724213,Human_Splice_Rec_724215,Human_Splice_Rec_724245,Human_Splice_Rec_724253,Human_Splice_Rec_724257 63036 RMVar_ID_63036 Human_SNP_ID_262906549 m1A Human chr5 - 177098006 177098003 177098006 CGTCAAGACGCTGGGGCAGCAGCAGCAGGGGGAGGTGTGGGGAAAGGGGGTTCAGAGGCCCAGAA CGTCAAGACGCTGGGGCAGCAGCAGCAGGGGG___TGTGGGGAAAGGGGGTTCAGAGGCCCAGAA ACCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177097959..177098052 26863196 MeRIP-seq:(Medium) rs995296430 Functional Loss DEL dbSNP153 33..35 33 - - - 63037 RMVar_ID_63037 Human_SNP_ID_262962487 m1A Human chr5 - 177304757 177304757 177304757 ACAATAGAGTCCTCCAGGACGTACACCGAGTGAGCAACATTGGCAGGAAATAGTCGCTCGGCCCA ACAATAGAGTCCTCCAGGACGTACACCGAGTGGGCAACATTGGCAGGAAATAGTCGCTCGGCCCA T C MXD3 Ensembl:ENSG00000213347 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177301510..177305515 32194978 MeRIP-seq:(Medium) rs774170605 Functional Loss SNV dbSNP153 33..33 33 - - - 63038 RMVar_ID_63038 Human_SNP_ID_262962925 m1A Human chr5 + 177306080 177306080 177306080 CTGGGGTCAGTGGGCAACTCAGTATCCTTCCCATTCTCATCTCATGCCAGGAATTTGGTCTTGCC CTGGGGTCAGTGGGCAACTCAGTATCCTTCCCGTTCTCATCTCATGCCAGGAATTTGGTCTTGCC A G PRELID1 Ensembl:ENSG00000169230 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177306076..177306125 32194978 MeRIP-seq:(Medium) rs377667935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943176,Human_RBP_ID_5397729,Human_RBP_ID_19015339,Human_RBP_ID_19125024 Human_Splice_Rec_724685,Human_Splice_Rec_724703,Human_Splice_Rec_724711,Human_Splice_Rec_724721 63039 RMVar_ID_63039 Human_SNP_ID_262962926 m1A Human chr5 + 177306080 177306080 177306080 CTGGGGTCAGTGGGCAACTCAGTATCCTTCCCATTCTCATCTCATGCCAGGAATTTGGTCTTGCC CTGGGGTCAGTGGGCAACTCAGTATCCTTCCCTTTCTCATCTCATGCCAGGAATTTGGTCTTGCC A T PRELID1 Ensembl:ENSG00000169230 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177306076..177306125 32194978 MeRIP-seq:(Medium) rs377667935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943176,Human_RBP_ID_5397729,Human_RBP_ID_19015339,Human_RBP_ID_19125024 Human_Splice_Rec_724685,Human_Splice_Rec_724703,Human_Splice_Rec_724711,Human_Splice_Rec_724721 63040 RMVar_ID_63040 Human_SNP_ID_262963174 m1A Human chr5 - 177306691 177306691 177306691 TTGGTGTACTGCAGATGCCAAACTGCATCCCCACAACCCACCACGTAGACAGCAGACAGGGCTGG TTGGTGTACTGCAGATGCCAAACTGCATCCCCGCAACCCACCACGTAGACAGCAGACAGGGCTGG T C MXD3 Ensembl:ENSG00000213347 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177306401..177306903 32194978 MeRIP-seq:(Medium) rs1349702585 Functional Loss SNV dbSNP153 33..33 33 - - - 63041 RMVar_ID_63041 Human_SNP_ID_262963476 m1A Human chr5 - 177307492 177307492 177307492 CCCTCCCCAAGCCTTCAGGGCTGCTCGGAGTCACCTGTTGGAATGGACTAAAAGGACCCTTGTGT CCCTCCCCAAGCCTTCAGGGCTGCTCGGAGTCGCCTGTTGGAATGGACTAAAAGGACCCTTGTGT T C MXD3 Ensembl:ENSG00000213347 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177307298..177307993 32194978 MeRIP-seq:(Medium) rs1309184574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638859,Human_RBP_ID_1651291,Human_RBP_ID_5151379,Human_RBP_ID_7421420,Human_RBP_ID_8611326,Human_RBP_ID_15398880,Human_RBP_ID_18045475,Human_RBP_ID_18170731,Human_RBP_ID_24099043 63042 RMVar_ID_63042 Human_SNP_ID_262963712 m1A Human chr5 - 177307863 177307858 177307863 CAGCGGCAGCTGGAGCAGCTCCGGGGGCTGGCAGGGGCGGCCGAGCGGGAGCGGCTGCGGGCGGA CAGCGGCAGCTGGAGCAGCTCCGGGGGCTGGC_____CGGCCGAGCGGGAGCGGCTGCGGGCGGA GCCCCT G MXD3 Ensembl:ENSG00000213347 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177307575..177307990 26863196 MeRIP-seq:(Medium) rs775604186 Functional Loss DEL dbSNP153 33..37 33 - - - Human_Splice_Rec_724597,Human_Splice_Rec_724613,Human_Splice_Rec_724627,Human_Splice_Rec_724645,Human_Splice_Rec_724651,Human_Splice_Rec_724663 Human_miRNA_ID_210104,Human_miRNA_ID_884566 RMVar_hsa_circ_13796 63043 RMVar_ID_63043 Human_SNP_ID_262963720 m1A Human chr5 - 177307863 177307863 177307863 CAGCGGCAGCTGGAGCAGCTCCGGGGGCTGGCAGGGGCGGCCGAGCGGGAGCGGCTGCGGGCGGA CAGCGGCAGCTGGAGCAGCTCCGGGGGCTGGCCGGGGCGGCCGAGCGGGAGCGGCTGCGGGCGGA T G MXD3 Ensembl:ENSG00000213347 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177307575..177307990 26863196 MeRIP-seq:(Medium) rs772139622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_724597,Human_Splice_Rec_724613,Human_Splice_Rec_724627,Human_Splice_Rec_724645,Human_Splice_Rec_724651,Human_Splice_Rec_724663 Human_miRNA_ID_210104,Human_miRNA_ID_884566 RMVar_hsa_circ_13796 63044 RMVar_ID_63044 Human_SNP_ID_262963722 m1A Human chr5 + 177307867 177307867 177307867 CCCGCAGCCGCTCCCGCTCGGCCGCCCCTGCCAGCCCCCGGAGCTGCTCCAGCTGCCGCTGCAGG CCCGCAGCCGCTCCCGCTCGGCCGCCCCTGCCGGCCCCCGGAGCTGCTCCAGCTGCCGCTGCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:177307353..177310700;chr5:177307651..177308019 26863196 MeRIP-seq:(Medium) rs775555092 Functional Loss SNV dbSNP153 33..33 33 - - - 63045 RMVar_ID_63045 Human_SNP_ID_262964906 m1A Human chr5 - 177311775 177311775 177311775 CCAGGTCCTGCTGCAGGCGGCCGAGTTCCTGGAGCGCCGTGAGAGAGGTGAGGAAGGACCCTTGG CCAGGTCCTGCTGCAGGCGGCCGAGTTCCTGGTGCGCCGTGAGAGAGGTGAGGAAGGACCCTTGG T A MXD3 Ensembl:ENSG00000213347 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177311749..177311900 26863196 MeRIP-seq:(Medium) rs1561596465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251003,Human_RBP_ID_19016199,Human_RBP_ID_26352930 Human_Splice_Rec_724593,Human_Splice_Rec_724619,Human_Splice_Rec_724629,Human_Splice_Rec_724637,Human_Splice_Rec_724647,Human_Splice_Rec_724655,Human_Splice_Rec_724665,Human_Splice_Rec_724673 63046 RMVar_ID_63046 Human_SNP_ID_262964931 m1A Human chr5 + 177311838 177311838 177311838 GGATGTTGCTGGCCAAGGGTTCCATGTCGGCGACAGCTGGCGGCGGGCCGGCCTAGGGTGCCGGC GGATGTTGCTGGCCAAGGGTTCCATGTCGGCGTCAGCTGGCGGCGGGCCGGCCTAGGGTGCCGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:177311346..177311900;chr5:177311702..177311900;chr5:177311351..177311925;chr5:177311395..177312251;chr5:177311340..177311900 26863196 MeRIP-seq:(Medium) rs1434049782 Functional Loss SNV dbSNP153 33..33 33 - - - 63047 RMVar_ID_63047 Human_SNP_ID_262965319 m1A Human chr5 + 177313007 177313000 177313008 CAGCCCCTGCTTGCCTTACTCAGAGTCCATAAACCCTTCTTGCACCTGACTCTCCTAGCCGGCCG CAGCCCCTGCTTGCCTTACTCAGAGT________CCTTCTTGCACCTGACTCTCCTAGCCGGCCG TCCATAAAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177312959..177313057 26863196 MeRIP-seq:(Medium) rs1394933260 Functional Loss DEL dbSNP153 27..34 33 - - - 63048 RMVar_ID_63048 Human_SNP_ID_262967050 m1A Human chr5 + 177319931 177319931 177319931 CCTTCCAACCACCTCCTTTACTGGGCTCTTACACGCTGCACCACTATCCCCCAGAGACTGGACAA CCTTCCAACCACCTCCTTTACTGGGCTCTTACGCGCTGCACCACTATCCCCCAGAGACTGGACAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177319893..177320077 26863196 MeRIP-seq:(Medium) rs1259308301 Functional Loss SNV dbSNP153 33..33 33 - - - 63049 RMVar_ID_63049 Human_SNP_ID_262970886 m1A Human chr5 + 177332065 177332065 177332065 AAAAGTTCACATTGGCTCCTGGGCCCAGGGACAGGCCCCGCCGGAGGCGCCACTCAGTAGAAGCG AAAAGTTCACATTGGCTCCTGGGCCCAGGGACCGGCCCCGCCGGAGGCGCCACTCAGTAGAAGCG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177332001..177334425 32194978 MeRIP-seq:(Medium) rs374827953 Functional Loss SNV dbSNP153 33..33 33 - - - 63050 RMVar_ID_63050 Human_SNP_ID_262970887 m1A Human chr5 + 177332065 177332065 177332065 AAAAGTTCACATTGGCTCCTGGGCCCAGGGACAGGCCCCGCCGGAGGCGCCACTCAGTAGAAGCG AAAAGTTCACATTGGCTCCTGGGCCCAGGGACGGGCCCCGCCGGAGGCGCCACTCAGTAGAAGCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177332001..177334425 32194978 MeRIP-seq:(Medium) rs374827953 Functional Loss SNV dbSNP153 33..33 33 - - - 63051 RMVar_ID_63051 Human_SNP_ID_262970914 m1A Human chr5 - 177332120 177332120 177332120 TGTCTGCGCCGTGGTGGGGGCCGTGGTGTTCCAGAAGCGGCAGGAGCGGAACAAGCGCTTCTACT TGTCTGCGCCGTGGTGGGGGCCGTGGTGTTCCTGAAGCGGCAGGAGCGGAACAAGCGCTTCTACT T A LMAN2 Ensembl:ENSG00000169223 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:177332101..177332175 26863196 MeRIP-seq:(Medium) rs1390264975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76640,Human_RBP_ID_638890,Human_RBP_ID_18057868,Human_RBP_ID_18501915,Human_RBP_ID_22099860,Human_RBP_ID_22459041,Human_RBP_ID_22772179 Human_miRNA_ID_1134088 RMVar_hsa_circ_106301,RMVar_hsa_circ_119385,RMVar_hsa_circ_123055,RMVar_hsa_circ_121661,RMVar_hsa_circ_110017,RMVar_hsa_circ_236475,RMVar_hsa_circ_236479,RMVar_hsa_circ_85106,RMVar_hsa_circ_102106,RMVar_hsa_circ_236480,RMVar_hsa_circ_236481,RMVar_hsa_circ_236477,RMVar_hsa_circ_236478,RMVar_hsa_circ_236476 63052 RMVar_ID_63052 Human_SNP_ID_262971445 m1A Human chr5 + 177333852 177333850 177333853 TAGCTAAGGAATCCACCCCCTTGACCAGCAGCACGACTTCTTCCAGGTGGCTCACAGAAGGGACA TAGCTAAGGAATCCACCCCCTTGACCAGCAG___GACTTCTTCCAGGTGGCTCACAGAAGGGACA GCAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177333848..177334044 26863196 MeRIP-seq:(Medium) rs201228031 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_236482 63053 RMVar_ID_63053 Human_SNP_ID_262972428 m1A Human chr5 + 177337130 177337130 177337130 GCTGGGCTGGGAACCAACGCCTGGCCCGGCCCACTCACCAGACAGGTCGCCGGTGCCGGCGGAGG GCTGGGCTGGGAACCAACGCCTGGCCCGGCCCCCTCACCAGACAGGTCGCCGGTGCCGGCGGAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177337126..177337469 32194978 MeRIP-seq:(Medium) rs771726847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236482 63054 RMVar_ID_63054 Human_SNP_ID_262972570 m1A Human chr5 + 177337421 177337421 177337421 CAGCCAGGAAGGTGTCGTGATCGCGGTTGCGGAAGTCAGCCGTGCAGCCCGCCAGCTCGGTCCAG CAGCCAGGAAGGTGTCGTGATCGCGGTTGCGGGAGTCAGCCGTGCAGCCCGCCAGCTCGGTCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177337142..177337541 26863196 MeRIP-seq:(Medium) rs1047166239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236485 63055 RMVar_ID_63055 Human_SNP_ID_262972660 m1A Human chr5 + 177337664 177337664 177337664 GTCCCAGGGCCCCCTCCTCTAGCCGACTGCCCAGTCCTTCCTTTCCTGCTCAGCAGGATAGAGCA GTCCCAGGGCCCCCTCCTCTAGCCGACTGCCCCGTCCTTCCTTTCCTGCTCAGCAGGATAGAGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177337660..177337794 26863196 MeRIP-seq:(Medium) rs371960732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236485 63056 RMVar_ID_63056 Human_SNP_ID_262972703 m1A Human chr5 + 177337777 177337777 177337777 GGCTAAGCCGTGGAAGTTATCTTTGCTTCCAAACACAGGCCCTAGAATTATAAGCAGATGCTCTC GGCTAAGCCGTGGAAGTTATCTTTGCTTCCAATCACAGGCCCTAGAATTATAAGCAGATGCTCTC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177337726..177337800 32194978 MeRIP-seq:(Medium) rs1340284988 Functional Loss SNV dbSNP153 33..33 33 - - - 63057 RMVar_ID_63057 Human_SNP_ID_262976663 m1A Human chr5 + 177351547 177351547 177351547 CCGCAGTCACAGACCCCAACAACAAAAGAAGAAAGAGAGGTGTAGTGGGGCCAGGGCCGGGGCCG CCGCAGTCACAGACCCCAACAACAAAAGAAGATAGAGAGGTGTAGTGGGGCCAGGGCCGGGGCCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177351498..177351675 26863196 MeRIP-seq:(Medium) rs1471535429 Functional Loss SNV dbSNP153 33..33 33 - - - 63058 RMVar_ID_63058 Human_SNP_ID_262976674 m1A Human chr5 + 177351567 177351567 177351567 AACAAAAGAAGAAAGAGAGGTGTAGTGGGGCCAGGGCCGGGGCCGAGAAGCCCAGGCCTTCCCAG AACAAAAGAAGAAAGAGAGGTGTAGTGGGGCCGGGGCCGGGGCCGAGAAGCCCAGGCCTTCCCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177351526..177351575 26863196 MeRIP-seq:(Medium) rs777909101 Functional Loss SNV dbSNP153 33..33 33 - - - 63059 RMVar_ID_63059 Human_SNP_ID_262976725 m1A Human chr5 - 177351636 177351636 177351636 AGTGGCCGAGAGGAGAGGAGAATGGCGGCGGAAGGCTGGATTTGGCGTTGGGGCTGGGGCCGGCG AGTGGCCGAGAGGAGAGGAGAATGGCGGCGGACGGCTGGATTTGGCGTTGGGGCTGGGGCCGGCG T G LMAN2 Ensembl:ENSG00000169223 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:177351541..177351635 26863410 MeRIP-seq:(Medium) rs1284825049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76646,Human_RBP_ID_4846927,Human_RBP_ID_5326654,Human_RBP_ID_22459047,Human_RBP_ID_23043011 Human_miRNA_ID_2898155,Human_miRNA_ID_2972904,Human_miRNA_ID_3006089 RMVar_hsa_circ_123055,RMVar_hsa_circ_236475,RMVar_hsa_circ_109674,RMVar_hsa_circ_236484 63060 RMVar_ID_63060 Human_SNP_ID_262981842 m1A Human chr5 - 177370899 177370899 177370899 ACGCGCTCCAGCGCCGTCAGCTCCAGCCTGCGAGGAACCCTCGGGCAGCAGAGGGCCGGAGGGCC ACGCGCTCCAGCGCCGTCAGCTCCAGCCTGCGGGGAACCCTCGGGCAGCAGAGGGCCGGAGGGCC T C lnc-LMAN2-1,lnc-LMAN2-1:2 RNACentral:URS00008B3CCF,RNACentral:URS00008B9985 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177370891..177370998 26863196 MeRIP-seq:(Medium) rs773059955 Functional Loss SNV dbSNP153 33..33 33 - - - 63061 RMVar_ID_63061 Human_SNP_ID_262982270 m1A Human chr5 + 177371377 177371377 177371377 TGCAGGTGTGAAGATCTCCAAAGCCCGTGACAAATCTCCCTGCCGCAGCCAGGTGAGCGAAAGGC TGCAGGTGTGAAGATCTCCAAAGCCCGTGACAGATCTCCCTGCCGCAGCCAGGTGAGCGAAAGGC A G RGS14 Ensembl:ENSG00000169220 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177371368..177371469 32194978 MeRIP-seq:(Medium) rs369021424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944827,Human_RBP_ID_1212054 Human_Splice_Rec_724822,Human_Splice_Rec_724823,Human_Splice_Rec_724854,Human_Splice_Rec_724855,Human_Splice_Rec_724884,Human_Splice_Rec_724885,Human_Splice_Rec_724894,Human_Splice_Rec_724895,Human_Splice_Rec_724900,Human_Splice_Rec_724901,Human_Splice_Rec_724906,Human_Splice_Rec_724908,Human_Splice_Rec_724909,Human_Splice_Rec_724912,Human_Splice_Rec_724913 RMVar_hsa_circ_24416,RMVar_hsa_circ_126387,RMVar_hsa_circ_236486 63062 RMVar_ID_63062 Human_SNP_ID_262991346 m1A Human chr5 - 177402700 177402699 177402700 GATGGGGTGTGAAGAAGGCGCTCTGTGTTCGCAGGGGCGGAGGAATATGCCAGCTTCCTGCAGGA GATGGGGTGTGAAGAAGGCGCTCTGTGTTCGC_GGGGCGGAGGAATATGCCAGCTTCCTGCAGGA CT C F12 Ensembl:ENSG00000131187 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177402674..177402823 32194978 MeRIP-seq:(Medium) rs1276865135 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_98000,RMVar_hsa_circ_106089,RMVar_hsa_circ_236488,RMVar_hsa_circ_236489 63063 RMVar_ID_63063 Human_SNP_ID_262991692 m1A Human chr5 - 177403619 177403619 177403619 TGAGAGCGCTGCCTCTCCCCTACCCCCCCCGCAGGCCCGCACCCGAGGATCTGACGGTGGTGCTC TGAGAGCGCTGCCTCTCCCCTACCCCCCCCGCGGGCCCGCACCCGAGGATCTGACGGTGGTGCTC T C F12 Ensembl:ENSG00000131187 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177403608..177403707 32194978 MeRIP-seq:(Medium) rs1385540500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4824877 RMVar_hsa_circ_98000,RMVar_hsa_circ_106089,RMVar_hsa_circ_236488,RMVar_hsa_circ_236489 63064 RMVar_ID_63064 Human_SNP_ID_262992066 m1A Human chr5 - 177404325 177404325 177404325 GCTGGGAGTACTGCGACCTGGCACAGTGCCAGACCCCAACCCAGGCGGCGCCTCCGACCCCGGTG GCTGGGAGTACTGCGACCTGGCACAGTGCCAGTCCCCAACCCAGGCGGCGCCTCCGACCCCGGTG T A F12 Ensembl:ENSG00000131187 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:177404234..177404401 26863410 MeRIP-seq:(Medium) rs766755922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_725002,Human_Splice_Rec_725034 RMVar_hsa_circ_98000,RMVar_hsa_circ_106089,RMVar_hsa_circ_236488,RMVar_hsa_circ_236489 63065 RMVar_ID_63065 Human_SNP_ID_262998177 m1A Human chr5 + 177426829 177426807 177426829 CGATCCCGGCCGGCGGCGCGGCCCGGCGGGCCAGGCGGCGCCACAGCCCATGGAGCTCGAGAACA CGATCCCGGCC______________________GGCGGCGCCACAGCCCATGGAGCTCGAGAACA CGGCGGCGCGGCCCGGCGGGCCA C GRK6 Ensembl:ENSG00000198055 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177426712..177426849 26863196 MeRIP-seq:(Medium) rs1282891330 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_250480,Human_RBP_ID_4845522,Human_RBP_ID_5151201,Human_RBP_ID_18195173 Human_Splice_Rec_725069,Human_Splice_Rec_725099,Human_Splice_Rec_725123,Human_Splice_Rec_725153,Human_Splice_Rec_725183,Human_Splice_Rec_725211 RMVar_hsa_circ_103816,RMVar_hsa_circ_114813,RMVar_hsa_circ_236490,RMVar_hsa_circ_236491 63066 RMVar_ID_63066 Human_SNP_ID_263003600 m1A Human chr5 - 177446850 177446850 177446850 TGCGGGGGGAGGCGGCGGCGGCCCGGGGGAGCAGACAGTGGCAGCGAAAGCGGCTCCGAGCGCTG TGCGGGGGGAGGCGGCGGCGGCCCGGGGGAGCCGACAGTGGCAGCGAAAGCGGCTCCGAGCGCTG T G PRR7-AS1 Ensembl:ENSG00000246334 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177446801..177448344 26863196 MeRIP-seq:(Medium) rs1452680002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944835,Human_RBP_ID_3783468,Human_RBP_ID_4845525,Human_RBP_ID_5213844,Human_RBP_ID_5614681,Human_RBP_ID_8213306,Human_RBP_ID_8730197,Human_RBP_ID_9436629,Human_RBP_ID_18425224,Human_RBP_ID_18465426,Human_RBP_ID_22364807,Human_RBP_ID_22418626,Human_RBP_ID_22727664,Human_RBP_ID_24554412,Human_RBP_ID_26791964 RMVar_hsa_circ_86447,RMVar_hsa_circ_236498 63067 RMVar_ID_63067 Human_SNP_ID_263004897 m1A Human chr5 + 177452208 177452208 177452208 TCAAATGGCAGACTTCGGTCCATCTGCAGGGCATCGCTCCGAGCACCTGAATGTGTTGGGTAGGT TCAAATGGCAGACTTCGGTCCATCTGCAGGGCGTCGCTCCGAGCACCTGAATGTGTTGGGTAGGT A G PRR7 Ensembl:ENSG00000131188 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177452203..177452310 26863196 MeRIP-seq:(Medium) rs942210130 Functional Loss SNV dbSNP153 33..33 33 - - - 63068 RMVar_ID_63068 Human_SNP_ID_263005576 m1A Human chr5 - 177454815 177454813 177454815 ACCCGGGGCCGCGCGGGACCTGTAGGGCAGACACGGGGCGCAGTGAAGGCGCGCCGCGGCCCCCA ACCCGGGGCCGCGCGGGACCTGTAGGGCAGAC__GGGGCGCAGTGAAGGCGCGCCGCGGCCCCCA CGT C PRR7-AS1 RNACentral:URS0000D5DF78 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177454813..177455102 26863196 MeRIP-seq:(Medium) rs1193547186 Functional Loss DEL dbSNP153 33..34 33 - - - 63069 RMVar_ID_63069 Human_SNP_ID_263006068 m1A Human chr5 + 177455977 177455977 177455977 CCCAGCGCCCCTCGGCCCGCGCCGCCCTGCCCAGCCCTCTGCCTGCAGGCCGACCGTGGCCGCCG CCCAGCGCCCCTCGGCCCGCGCCGCCCTGCCCCGCCCTCTGCCTGCAGGCCGACCGTGGCCGCCG A C PRR7 Ensembl:ENSG00000131188 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177455708..177456208 26863196 MeRIP-seq:(Medium) rs769025501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167008,Human_RBP_ID_638983,Human_RBP_ID_5121492,Human_RBP_ID_18045524 63070 RMVar_ID_63070 Human_SNP_ID_263006589 m1A Human chr5 - 177457223 177457223 177457223 CTCTTTTTTTAAAAAGTTGATAGGAGACTTGTACAGTTGACTGGCTTTCCTCTCGTTGGTAGTTG CTCTTTTTTTAAAAAGTTGATAGGAGACTTGTGCAGTTGACTGGCTTTCCTCTCGTTGGTAGTTG T C DBN1 Ensembl:ENSG00000113758 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177456756..177457525 32194978 MeRIP-seq:(Medium) rs948532361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639005,Human_RBP_ID_1212067,Human_RBP_ID_1993089,Human_RBP_ID_5121494,Human_RBP_ID_7421562,Human_RBP_ID_18357091,Human_RBP_ID_26530175,Human_RBP_ID_26701661,Human_RBP_ID_27079112 RMVar_hsa_circ_86252,RMVar_hsa_circ_121989,RMVar_hsa_circ_236499,RMVar_hsa_circ_236500 63071 RMVar_ID_63071 Human_SNP_ID_263007245 m1A Human chr5 - 177458701 177458701 177458701 TATCTCCTCTGCCTGTGCTGTGACAGAGACCCAGGAGCCCAGCCCCATCCTAGACAGTGAGGAGA TATCTCCTCTGCCTGTGCTGTGACAGAGACCCTGGAGCCCAGCCCCATCCTAGACAGTGAGGAGA T A DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr5:177458058..177458738;chr5:177458651..177458725;chr5:177458438..177458725 26863196 MeRIP-seq:(Medium) rs1486836330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943588,Human_RBP_ID_22553415,Human_RBP_ID_22613855 Human_Splice_Rec_725306,Human_Splice_Rec_725334,Human_Splice_Rec_725358,Human_Splice_Rec_725386,Human_Splice_Rec_725398,Human_Splice_Rec_725402 RMVar_hsa_circ_86252,RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_121397,RMVar_hsa_circ_236499,RMVar_hsa_circ_236500,RMVar_hsa_circ_236502 63072 RMVar_ID_63072 Human_SNP_ID_263007359 m1A Human chr5 + 177459085 177459085 177459085 GGACTGATGATGGGAGGCCTGGTGCAGGTAGCATCCCTCTCTCACCTTGGGCTGGTGGGGGTGGC GGACTGATGATGGGAGGCCTGGTGCAGGTAGCGTCCCTCTCTCACCTTGGGCTGGTGGGGGTGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177459076..177459317 26863196 MeRIP-seq:(Medium) rs775803342 Functional Loss SNV dbSNP153 33..33 33 - - - 63073 RMVar_ID_63073 Human_SNP_ID_263007403 m1A Human chr5 - 177459166 177459166 177459166 CACCGCCTCCACCCCTGTCGCTGAGCAGATAGAGCGGGCCCTGGATGAGGTCACCTCCTCGCAGC CACCGCCTCCACCCCTGTCGCTGAGCAGATAGGGCGGGCCCTGGATGAGGTCACCTCCTCGCAGC T C DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:177459061..177459295;chr5:177459071..177459319 26863196 MeRIP-seq:(Medium) rs537160653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_787724,Human_RBP_ID_839660,Human_RBP_ID_5397752,Human_RBP_ID_22615515,Human_RBP_ID_27079136 Human_Splice_Rec_725305,Human_Splice_Rec_725333,Human_Splice_Rec_725357,Human_Splice_Rec_725385,Human_Splice_Rec_725397,Human_Splice_Rec_725401 Human_miRNA_ID_2572579,Human_miRNA_ID_2572580 RMVar_hsa_circ_86252,RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_121397,RMVar_hsa_circ_236499,RMVar_hsa_circ_236500,RMVar_hsa_circ_53146,RMVar_hsa_circ_236502,RMVar_hsa_circ_117081,RMVar_hsa_circ_236503 63074 RMVar_ID_63074 Human_SNP_ID_263007451 m1A Human chr5 - 177459266 177459266 177459266 TCACTGACCCACCTGGGGTTTGTTCCACAGGCAGCCACCTGGACAGCCACCGGAGGATGGCGCCC TCACTGACCCACCTGGGGTTTGTTCCACAGGCCGCCACCTGGACAGCCACCGGAGGATGGCGCCC T G DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177458694..177459618 32194978 MeRIP-seq:(Medium) rs1436390189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946591,Human_RBP_ID_9398711,Human_RBP_ID_22459408,Human_RBP_ID_22681289 Human_Splice_Rec_725304,Human_Splice_Rec_725332,Human_Splice_Rec_725356,Human_Splice_Rec_725384,Human_Splice_Rec_725396,Human_Splice_Rec_725400 RMVar_hsa_circ_86252,RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_121397,RMVar_hsa_circ_236499,RMVar_hsa_circ_236500,RMVar_hsa_circ_53146,RMVar_hsa_circ_236502,RMVar_hsa_circ_117081,RMVar_hsa_circ_236503 63075 RMVar_ID_63075 Human_SNP_ID_263007946 m1A Human chr5 - 177460687 177460687 177460687 TCCCTTTGGTTTCTAGGGTGACCATCGGGATGAGGAGGAAGAGACCCACATGAAGAAGTCAGAGT TCCCTTTGGTTTCTAGGGTGACCATCGGGATGCGGAGGAAGAGACCCACATGAAGAAGTCAGAGT T G DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:177460384..177460751;chr5:177460406..177460739;chr5:177460476..177460725 26863196 MeRIP-seq:(Medium) rs1358448745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74938,Human_RBP_ID_839663,Human_RBP_ID_946594,Human_RBP_ID_3967642,Human_RBP_ID_5396403,Human_RBP_ID_9398715,Human_RBP_ID_17671692,Human_RBP_ID_18413633,Human_RBP_ID_19015347,Human_RBP_ID_22681060,Human_RBP_ID_26351811,Human_RBP_ID_26771688,Human_RBP_ID_26827713,Human_RBP_ID_27826136 Human_Splice_Rec_725300,Human_Splice_Rec_725301,Human_Splice_Rec_725328,Human_Splice_Rec_725329,Human_Splice_Rec_725352,Human_Splice_Rec_725353,Human_Splice_Rec_725378,Human_Splice_Rec_725379,Human_Splice_Rec_725392,Human_Splice_Rec_725393,Human_Splice_Rec_725418,Human_Splice_Rec_725419 Human_miRNA_ID_2297126,Human_miRNA_ID_2297127 RMVar_hsa_circ_29213,RMVar_hsa_circ_86252,RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_121397,RMVar_hsa_circ_236499,RMVar_hsa_circ_236500,RMVar_hsa_circ_53146,RMVar_hsa_circ_236502,RMVar_hsa_circ_117081,RMVar_hsa_circ_312654,RMVar_hsa_circ_236503,RMVar_hsa_circ_45910 63076 RMVar_ID_63076 Human_SNP_ID_263010018 m1A Human chr5 - 177466834 177466834 177466834 CCTGACGGGTGCTGGCTGCTTATCGTTCCAGGAGGAAACAGCAGACTTTAGAAGCGGAAGAGGCC CCTGACGGGTGCTGGCTGCTTATCGTTCCAGGGGGAAACAGCAGACTTTAGAAGCGGAAGAGGCC T C DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177466751..177466850 32194978 MeRIP-seq:(Medium) rs1344989054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74939,Human_RBP_ID_19126855,Human_RBP_ID_26351813 Human_Splice_Rec_725298,Human_Splice_Rec_725299,Human_Splice_Rec_725326,Human_Splice_Rec_725327,Human_Splice_Rec_725350,Human_Splice_Rec_725351,Human_Splice_Rec_725376,Human_Splice_Rec_725377,Human_Splice_Rec_725416,Human_Splice_Rec_725417 RMVar_hsa_circ_29213,RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_121397,RMVar_hsa_circ_236500,RMVar_hsa_circ_53146,RMVar_hsa_circ_236502,RMVar_hsa_circ_117081,RMVar_hsa_circ_312654,RMVar_hsa_circ_236503,RMVar_hsa_circ_45910 63077 RMVar_ID_63077 Human_SNP_ID_263010829 m1A Human chr5 - 177468828 177468828 177468828 GCTTGCAGCATCAGGAGGTAGGAATTCCAGCCATTCCCTCGCCGCCTTCTCCACCCCCTCCTCCT GCTTGCAGCATCAGGAGGTAGGAATTCCAGCCCTTCCCTCGCCGCCTTCTCCACCCCCTCCTCCT T G DBN1 Ensembl:ENSG00000113758 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177468826..177472166 32194978 MeRIP-seq:(Medium) rs1395572555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126859 Human_Splice_Rec_725286,Human_Splice_Rec_725314,Human_Splice_Rec_725340,Human_Splice_Rec_725364,Human_Splice_Rec_725404,Human_Splice_Rec_725426,Human_Splice_Rec_725436,Human_Splice_Rec_725444 RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_236500,RMVar_hsa_circ_117081,RMVar_hsa_circ_236503,RMVar_hsa_circ_45910,RMVar_hsa_circ_34573 63078 RMVar_ID_63078 Human_SNP_ID_263010839 m1A Human chr5 + 177468858 177468858 177468858 AATGGCTGGAATTCCTACCTCCTGATGCTGCAAGCTTGAGGTCATCGGAGCCATCTTCATATGTG AATGGCTGGAATTCCTACCTCCTGATGCTGCAGGCTTGAGGTCATCGGAGCCATCTTCATATGTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177468851..177468900 26863196 MeRIP-seq:(Medium) rs769854465 Functional Loss SNV dbSNP153 33..33 33 - - - 63079 RMVar_ID_63079 Human_SNP_ID_263010988 m1A Human chr5 - 177469296 177469296 177469296 CTCCCCGGGGGAGGGGCAGCGGGGACCAAGGCACGTGCCAGGTAAGTTCCTGGCACTAGCCAATG CTCCCCGGGGGAGGGGCAGCGGGGACCAAGGCCCGTGCCAGGTAAGTTCCTGGCACTAGCCAATG T G DBN1 Ensembl:ENSG00000113758 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177469293..177469423 26863196 MeRIP-seq:(Medium) rs768293012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121989,RMVar_hsa_circ_236500 63080 RMVar_ID_63080 Human_SNP_ID_263011014 m1A Human chr5 + 177469360 177469359 177469360 GGGAGGAGGAGAAGAGAGAACCTGGTGCTCCCAACAGCTCTGGGCATCCCCCAGTAACCATGGCA GGGAGGAGGAGAAGAGAGAACCTGGTGCTCCC_ACAGCTCTGGGCATCCCCCAGTAACCATGGCA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177469356..177469464 26863196 MeRIP-seq:(Medium) rs1468783025 Functional Loss DEL dbSNP153 33..33 33 - - - 63081 RMVar_ID_63081 Human_SNP_ID_263011855 m1A Human chr5 + 177472199 177472199 177472199 CTGCTGGCCAGTGCTGCAGTACCATGCCATGGATGCCCAGCCATCTCATCCTCTCCTCCAGAAGC CTGCTGGCCAGTGCTGCAGTACCATGCCATGGGTGCCCAGCCATCTCATCCTCTCCTCCAGAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177472197..177472267 26863196 MeRIP-seq:(Medium) rs1243719968 Functional Loss SNV dbSNP153 33..33 33 - - - 63082 RMVar_ID_63082 Human_SNP_ID_263012380 m1A Human chr5 + 177473560 177473560 177473560 GGCCGGACCGGGCCGAACGGACAGACGCGCGGACGGACGGGCGGACGGAGGAGGAGGGAGGGAAA GGCCGGACCGGGCCGAACGGACAGACGCGCGGGCGGACGGGCGGACGGAGGAGGAGGGAGGGAAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:177473375..177473626 26863196 MeRIP-seq:(Medium) rs938242668 Functional Loss SNV dbSNP153 33..33 33 - - - 63083 RMVar_ID_63083 Human_SNP_ID_263013728 m1A Human chr5 - 177478342 177478342 177478342 GGCAGAGCCCATGGCAGGGGGCTGAGTGGGTAACTGGAGAGGCAGCAGGCAAGGGAGGGGTTTTT GGCAGAGCCCATGGCAGGGGGCTGAGTGGGTACCTGGAGAGGCAGCAGGCAAGGGAGGGGTTTTT T G AC145098.2 Ensembl:ENSG00000279821 Other exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177478336..177478423 26863196 MeRIP-seq:(Medium) rs1040049673 Functional Loss SNV dbSNP153 33..33 33 - - - 63084 RMVar_ID_63084 Human_SNP_ID_263014905 m1A Human chr5 - 177482594 177482592 177482594 TTGAAATAGGTTTGTGTTGTATTGCAGAAAAGAGGCCCCAGAACACTGAGGGAGTGCAGGAGGGA TTGAAATAGGTTTGTGTTGTATTGCAGAAAAG__GCCCCAGAACACTGAGGGAGTGCAGGAGGGA CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:177482576..177482727 26863196 MeRIP-seq:(Medium) rs1429106488 Functional Loss DEL dbSNP153 33..34 33 - - - 63085 RMVar_ID_63085 Human_SNP_ID_263015162 m1A Human chr5 - 177483502 177483502 177483502 GCCCGAGCCTGGGGCTCCCTGGGCCCTGCCCCACCCACCTTATCCTCCCACCCCACTCCCTCCAC GCCCGAGCCTGGGGCTCCCTGGGCCCTGCCCCCCCCACCTTATCCTCCCACCCCACTCCCTCCAC T G PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177483451..177483725 26863196 MeRIP-seq:(Medium) rs1448648328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165994,Human_RBP_ID_17090152,Human_RBP_ID_18956307,Human_RBP_ID_27079162 Human_miRNA_ID_1705278 RMVar_hsa_circ_101676,RMVar_hsa_circ_123362,RMVar_hsa_circ_236506,RMVar_hsa_circ_236507 63086 RMVar_ID_63086 Human_SNP_ID_263015170 m1A Human chr5 + 177483519 177483519 177483519 GGAGGATAAGGTGGGTGGGGCAGGGCCCAGGGAGCCCCAGGCTCGGGCCAGGAGCCAGGGTTAAG GGAGGATAAGGTGGGTGGGGCAGGGCCCAGGGGGCCCCAGGCTCGGGCCAGGAGCCAGGGTTAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:177483478..177483586;chr5:177483469..177483584 26863196 MeRIP-seq:(Medium) rs1442401311 Functional Loss SNV dbSNP153 33..33 33 - - - 63087 RMVar_ID_63087 Human_SNP_ID_263017177 m1A Human chr5 - 177489402 177489402 177489402 CGGCAAGACTCCCGTGTGTCACCAGTGCCACAAGGTCATCCGGTGGGTGGCCTGTTCCTGTCCGA CGGCAAGACTCCCGTGTGTCACCAGTGCCACAGGGTCATCCGGTGGGTGGCCTGTTCCTGTCCGA T C PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177488051..177491201 32194978 MeRIP-seq:(Medium) rs142855410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19015349 Human_Splice_Rec_725463,Human_Splice_Rec_725487,Human_Splice_Rec_725511,Human_Splice_Rec_725535,Human_Splice_Rec_725565 RMVar_hsa_circ_50409,RMVar_hsa_circ_33868,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510 63088 RMVar_ID_63088 Human_SNP_ID_263017273 m1A Human chr5 - 177489550 177489550 177489550 ACCCTGCGTTTGCCGAGCGCTATGCCCCGGACAAAACGAGCACAGTGCTGACCCGGCACAGCCAG ACCCTGCGTTTGCCGAGCGCTATGCCCCGGACGAAACGAGCACAGTGCTGACCCGGCACAGCCAG T C PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177489500..177489569 26863196 MeRIP-seq:(Medium) rs904209014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967645 Human_Splice_Rec_725462,Human_Splice_Rec_725486,Human_Splice_Rec_725510,Human_Splice_Rec_725534,Human_Splice_Rec_725564 RMVar_hsa_circ_50409,RMVar_hsa_circ_33868,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510 63089 RMVar_ID_63089 Human_SNP_ID_263017601 m1A Human chr5 - 177490302 177490302 177490302 TCTGACACTGCCTTCCCTCTTTGCCCTGTGGTACTGCTGTCTGCCAGGTCTGTGCTGCCTTGGGC TCTGACACTGCCTTCCCTCTTTGCCCTGTGGTTCTGCTGTCTGCCAGGTCTGTGCTGCCTTGGGC T A PDLIM7 Ensembl:ENSG00000196923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177490300..177490609 26863196 MeRIP-seq:(Medium) rs55786991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639021,Human_RBP_ID_8611469,Human_RBP_ID_9335485,Human_RBP_ID_18956308,Human_RBP_ID_21153795,Human_RBP_ID_22100350,Human_RBP_ID_24099232 RMVar_hsa_circ_50409,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510,RMVar_hsa_circ_236511,RMVar_hsa_circ_83298 63090 RMVar_ID_63090 Human_SNP_ID_263018012 m1A Human chr5 - 177491064 177491064 177491064 AGAACACAGAGGACTGGCGGCCGCGGCCGGGGACAGGCCAGTCGCGTTCCTTCCGCATCCTTGCC AGAACACAGAGGACTGGCGGCCGCGGCCGGGGCCAGGCCAGTCGCGTTCCTTCCGCATCCTTGCC T G PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177491026..177491100 26863196 MeRIP-seq:(Medium) rs770237475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_725456,Human_Splice_Rec_725457,Human_Splice_Rec_725480,Human_Splice_Rec_725481,Human_Splice_Rec_725504,Human_Splice_Rec_725505,Human_Splice_Rec_725528,Human_Splice_Rec_725529,Human_Splice_Rec_725560,Human_Splice_Rec_725561,Human_Splice_Rec_725576,Human_Splice_Rec_725577,Human_Splice_Rec_725590,Human_Splice_Rec_725591,Human_Splice_Rec_725604,Human_Splice_Rec_725612,Human_Splice_Rec_725624,Human_Splice_Rec_725634 RMVar_hsa_circ_50409,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510,RMVar_hsa_circ_359673 63091 RMVar_ID_63091 Human_SNP_ID_263018042 m1A Human chr5 - 177491100 177491100 177491100 CGCTGGTCCCAGATGCCAGCAAGCAGCGGCTGATGGAGAACACAGAGGACTGGCGGCCGCGGCCG CGCTGGTCCCAGATGCCAGCAAGCAGCGGCTGGTGGAGAACACAGAGGACTGGCGGCCGCGGCCG T C PDLIM7 Ensembl:ENSG00000196923 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177490826..177491356 26863196 MeRIP-seq:(Medium) rs1357037177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_725456,Human_Splice_Rec_725457,Human_Splice_Rec_725480,Human_Splice_Rec_725481,Human_Splice_Rec_725504,Human_Splice_Rec_725505,Human_Splice_Rec_725528,Human_Splice_Rec_725529,Human_Splice_Rec_725560,Human_Splice_Rec_725561,Human_Splice_Rec_725576,Human_Splice_Rec_725577,Human_Splice_Rec_725590,Human_Splice_Rec_725591,Human_Splice_Rec_725604,Human_Splice_Rec_725612,Human_Splice_Rec_725624,Human_Splice_Rec_725634 RMVar_hsa_circ_50409,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510,RMVar_hsa_circ_359673 63092 RMVar_ID_63092 Human_SNP_ID_263018043 m1A Human chr5 - 177491100 177491100 177491100 CGCTGGTCCCAGATGCCAGCAAGCAGCGGCTGATGGAGAACACAGAGGACTGGCGGCCGCGGCCG CGCTGGTCCCAGATGCCAGCAAGCAGCGGCTGCTGGAGAACACAGAGGACTGGCGGCCGCGGCCG T G PDLIM7 Ensembl:ENSG00000196923 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177490826..177491356 26863196 MeRIP-seq:(Medium) rs1357037177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_725456,Human_Splice_Rec_725457,Human_Splice_Rec_725480,Human_Splice_Rec_725481,Human_Splice_Rec_725504,Human_Splice_Rec_725505,Human_Splice_Rec_725528,Human_Splice_Rec_725529,Human_Splice_Rec_725560,Human_Splice_Rec_725561,Human_Splice_Rec_725576,Human_Splice_Rec_725577,Human_Splice_Rec_725590,Human_Splice_Rec_725591,Human_Splice_Rec_725604,Human_Splice_Rec_725612,Human_Splice_Rec_725624,Human_Splice_Rec_725634 RMVar_hsa_circ_50409,RMVar_hsa_circ_106894,RMVar_hsa_circ_236510,RMVar_hsa_circ_359673 63093 RMVar_ID_63093 Human_SNP_ID_263018385 m1A Human chr5 + 177491902 177491902 177491902 AGGGAGACGCTGGGTGCAAAGGTGTACCGCGGAGGGTCCGCGGCGGGGGCGGAGGCCTGGGCAGA AGGGAGACGCTGGGTGCAAAGGTGTACCGCGGCGGGTCCGCGGCGGGGGCGGAGGCCTGGGCAGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177491776..177491984 26863196 MeRIP-seq:(Medium) rs541858166 Functional Loss SNV dbSNP153 33..33 33 - - - 63094 RMVar_ID_63094 Human_SNP_ID_263018386 m1A Human chr5 + 177491902 177491902 177491902 AGGGAGACGCTGGGTGCAAAGGTGTACCGCGGAGGGTCCGCGGCGGGGGCGGAGGCCTGGGCAGA AGGGAGACGCTGGGTGCAAAGGTGTACCGCGGGGGGTCCGCGGCGGGGGCGGAGGCCTGGGCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177491776..177491984 26863196 MeRIP-seq:(Medium) rs541858166 Functional Loss SNV dbSNP153 33..33 33 - - - 63095 RMVar_ID_63095 Human_SNP_ID_263018691 m1A Human chr5 + 177492597 177492597 177492597 ATCTTGTTCTGAGCTTCGATGTGTGTGAGGCTACCCGCATTCTCGCCATCGATGCTCAGCACCCA ATCTTGTTCTGAGCTTCGATGTGTGTGAGGCTCCCCGCATTCTCGCCATCGATGCTCAGCACCCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:177492551..177492675 26863196 MeRIP-seq:(Medium) rs576141698 Functional Loss SNV dbSNP153 33..33 33 - - - 63096 RMVar_ID_63096 Human_SNP_ID_263018694 m1A Human chr5 + 177492603 177492603 177492603 TTCTGAGCTTCGATGTGTGTGAGGCTACCCGCATTCTCGCCATCGATGCTCAGCACCCAGTCACC TTCTGAGCTTCGATGTGTGTGAGGCTACCCGCGTTCTCGCCATCGATGCTCAGCACCCAGTCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:177492316..177492718;chr5:177491737..177492718 26863196 MeRIP-seq:(Medium) rs1296938320 Functional Loss SNV dbSNP153 33..33 33 - - - 63097 RMVar_ID_63097 Human_SNP_ID_263018717 m1A Human chr5 - 177492645 177492645 177492645 CTCACTCCTGGGGGCAAAGCGGCGCAGGCCGGAGTGGCCGTGGGTGACTGGGTGCTGAGCATCGA CTCACTCCTGGGGGCAAAGCGGCGCAGGCCGGGGTGGCCGTGGGTGACTGGGTGCTGAGCATCGA T C PDLIM7 Ensembl:ENSG00000196923 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177492601..177492650 26863196 MeRIP-seq:(Medium) rs1222248055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967657,Human_RBP_ID_8237004,Human_RBP_ID_9335843,Human_RBP_ID_9398721,Human_RBP_ID_19015354,Human_RBP_ID_22681069 Human_Splice_Rec_725448,Human_Splice_Rec_725474,Human_Splice_Rec_725498,Human_Splice_Rec_725522,Human_Splice_Rec_725554,Human_Splice_Rec_725570,Human_Splice_Rec_725584,Human_Splice_Rec_725598,Human_Splice_Rec_725606,Human_Splice_Rec_725626,Human_Splice_Rec_725638,Human_Splice_Rec_725642 RMVar_hsa_circ_50409,RMVar_hsa_circ_348647 63098 RMVar_ID_63098 Human_SNP_ID_263018731 m1A Human chr5 + 177492672 177492672 177492672 GCCACTCCGGCCTGCGCCGCTTTGCCCCCAGGAGTGAGCTGTGGAGAGAGAAGCAAAGTGACCGA GCCACTCCGGCCTGCGCCGCTTTGCCCCCAGGCGTGAGCTGTGGAGAGAGAAGCAAAGTGACCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177492429..177492718 26863196 MeRIP-seq:(Medium) rs1211939278 Functional Loss SNV dbSNP153 33..33 33 - - - 63099 RMVar_ID_63099 Human_SNP_ID_263020156 m1A Human chr5 + 177497543 177497543 177497543 CGCGCGGTCGTCGATACCTGCTTGGCCCGGCCAGGGCGCTGCTCTGCGTCGGGCTCCAGGGAGCC CGCGCGGTCGTCGATACCTGCTTGGCCCGGCCGGGGCGCTGCTCTGCGTCGGGCTCCAGGGAGCC A G AC145098.1 Ensembl:ENSG00000248996 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177497526..177497600 26863196 MeRIP-seq:(Medium) rs1196751636 Functional Loss SNV dbSNP153 33..33 33 - - - 63100 RMVar_ID_63100 Human_SNP_ID_263021699 m1A Human chr5 - 177503053 177503053 177503053 GCAACTCCACCTCAGCTGCACACACCCTTGGCACATCCTGAACCTCATTTTCATGACGGACACAC GCAACTCCACCTCAGCTGCACACACCCTTGGCTCATCCTGAACCTCATTTTCATGACGGACACAC T A DOK3 Ensembl:ENSG00000146094 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:177503015..177503193 26863196 MeRIP-seq:(Medium) rs1223854458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1651394,Human_RBP_ID_15400012 63101 RMVar_ID_63101 Human_SNP_ID_263022743 m1A Human chr5 + 177505461 177505461 177505461 AGAGCAGTACCCCAGGTGTCTTCCTCCATCTCACCACAGCCACCTGCTATGACCCTGCAAGGTGC AGAGCAGTACCCCAGGTGTCTTCCTCCATCTCGCCACAGCCACCTGCTATGACCCTGCAAGGTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177505457..177505606 26863196 MeRIP-seq:(Medium) rs1054172064 Functional Loss SNV dbSNP153 33..33 33 - - - 63102 RMVar_ID_63102 Human_SNP_ID_263024805 m1A Human chr5 - 177511810 177511810 177511810 CAGCAACATCGGTCGCAAGGACTACCTGGCCCACAGCTCCATGGACTTCTGAGCCGACAGTCTTC CAGCAACATCGGTCGCAAGGACTACCTGGCCCGCAGCTCCATGGACTTCTGAGCCGACAGTCTTC T C DDX41 Ensembl:ENSG00000183258 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177511762..177511847 26863196 MeRIP-seq:(Medium) rs771535420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1993103,Human_RBP_ID_15400137 Human_miRNA_ID_2661576,Human_miRNA_ID_2680023 RMVar_hsa_circ_98856,RMVar_hsa_circ_116282,RMVar_hsa_circ_121254,RMVar_hsa_circ_123225,RMVar_hsa_circ_119618,RMVar_hsa_circ_104283,RMVar_hsa_circ_106871,RMVar_hsa_circ_103086,RMVar_hsa_circ_236513,RMVar_hsa_circ_236521,RMVar_hsa_circ_87565,RMVar_hsa_circ_97351,RMVar_hsa_circ_98549,RMVar_hsa_circ_91677,RMVar_hsa_circ_236525,RMVar_hsa_circ_81286,RMVar_hsa_circ_86245,RMVar_hsa_circ_78752,RMVar_hsa_circ_236526,RMVar_hsa_circ_236523,RMVar_hsa_circ_236524,RMVar_hsa_circ_236522,RMVar_hsa_circ_236517,RMVar_hsa_circ_236519,RMVar_hsa_circ_236520,RMVar_hsa_circ_236518,RMVar_hsa_circ_236515,RMVar_hsa_circ_236516,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512 63103 RMVar_ID_63103 Human_SNP_ID_263024930 m1A Human chr5 - 177512128 177512128 177512128 GCAGAAGGTGCCGCCCGTGCTGCAGGTGCTGCATTGCGGGGATGAGTCCATGCTGGACATTGGAG GCAGAAGGTGCCGCCCGTGCTGCAGGTGCTGCGTTGCGGGGATGAGTCCATGCTGGACATTGGAG T C DDX41 Ensembl:ENSG00000183258 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1467756814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840073,Human_RBP_ID_3967658,Human_RBP_ID_18839268,Human_RBP_ID_19015357,Human_RBP_ID_22459051 Human_Splice_Rec_725734,Human_Splice_Rec_725735,Human_Splice_Rec_725766,Human_Splice_Rec_725767,Human_Splice_Rec_725798,Human_Splice_Rec_725799,Human_Splice_Rec_725822,Human_Splice_Rec_725823,Human_Splice_Rec_725852,Human_Splice_Rec_725853,Human_Splice_Rec_725868,Human_Splice_Rec_725869,Human_Splice_Rec_725888,Human_Splice_Rec_725889,Human_Splice_Rec_725914,Human_Splice_Rec_725915,Human_Splice_Rec_725944,Human_Splice_Rec_725945,Human_Splice_Rec_725972 RMVar_hsa_circ_98856,RMVar_hsa_circ_116282,RMVar_hsa_circ_121254,RMVar_hsa_circ_123225,RMVar_hsa_circ_119618,RMVar_hsa_circ_106871,RMVar_hsa_circ_103086,RMVar_hsa_circ_236513,RMVar_hsa_circ_236521,RMVar_hsa_circ_87565,RMVar_hsa_circ_97351,RMVar_hsa_circ_98549,RMVar_hsa_circ_91677,RMVar_hsa_circ_236525,RMVar_hsa_circ_81286,RMVar_hsa_circ_86245,RMVar_hsa_circ_78752,RMVar_hsa_circ_236523,RMVar_hsa_circ_236524,RMVar_hsa_circ_236522,RMVar_hsa_circ_236517,RMVar_hsa_circ_236519,RMVar_hsa_circ_236520,RMVar_hsa_circ_236518,RMVar_hsa_circ_236515,RMVar_hsa_circ_236516,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512 63104 RMVar_ID_63104 Human_SNP_ID_263025292 m1A Human chr5 + 177513039 177513039 177513039 TCACAGGCGGGGGTGTCTTCTGCAGGCACTCGAGCAGGTACACCATCTTGGCCTCCTCCTTCACA TCACAGGCGGGGGTGTCTTCTGCAGGCACTCGTGCAGGTACACCATCTTGGCCTCCTCCTTCACA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177512856..177513131 32194978 MeRIP-seq:(Medium) rs1323392935 Functional Loss SNV dbSNP153 33..33 33 - - - 63105 RMVar_ID_63105 Human_SNP_ID_263026424 m1A Human chr5 - 177515962 177515962 177515962 TTCAGCATTGATGTCAGTGAAGGAGATGGCTAAGGGCATTACGTATGATGACCCCATCAAAACCA TTCAGCATTGATGTCAGTGAAGGAGATGGCTAGGGGCATTACGTATGATGACCCCATCAAAACCA T C DDX41 Ensembl:ENSG00000183258 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177515727..177516027 26863196 MeRIP-seq:(Medium) rs774582005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18057475,Human_RBP_ID_19016254,Human_RBP_ID_24548158,Human_RBP_ID_26351842,Human_RBP_ID_26701667,Human_RBP_ID_27827152 Human_Splice_Rec_725744,Human_Splice_Rec_725745,Human_Splice_Rec_725776,Human_Splice_Rec_725777,Human_Splice_Rec_725830,Human_Splice_Rec_725831,Human_Splice_Rec_725894,Human_Splice_Rec_725895,Human_Splice_Rec_725922,Human_Splice_Rec_725923,Human_Splice_Rec_725952,Human_Splice_Rec_725953,Human_Splice_Rec_726015,Human_Splice_Rec_726024,Human_Splice_Rec_726025,Human_Splice_Rec_726038,Human_Splice_Rec_726039,Human_Splice_Rec_726052,Human_Splice_Rec_726053,Human_Splice_Rec_726064,Human_Splice_Rec_726065,Human_Splice_Rec_726080,Human_Splice_Rec_726081 RMVar_hsa_circ_98856,RMVar_hsa_circ_236513,RMVar_hsa_circ_97351,RMVar_hsa_circ_91677,RMVar_hsa_circ_81286,RMVar_hsa_circ_236515,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512,RMVar_hsa_circ_116257,RMVar_hsa_circ_126373,RMVar_hsa_circ_236530,RMVar_hsa_circ_236531,RMVar_hsa_circ_115290,RMVar_hsa_circ_236534,RMVar_hsa_circ_79462,RMVar_hsa_circ_236535 63106 RMVar_ID_63106 Human_SNP_ID_263026428 m1A Human chr5 - 177515979 177515979 177515979 TGAGCCATGTCTCTCTCTTCAGCATTGATGTCAGTGAAGGAGATGGCTAAGGGCATTACGTATGA TGAGCCATGTCTCTCTCTTCAGCATTGATGTCGGTGAAGGAGATGGCTAAGGGCATTACGTATGA T C DDX41 Ensembl:ENSG00000183258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177515926..177516000 26863196 MeRIP-seq:(Medium) rs200841282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18057475,Human_RBP_ID_19016254,Human_RBP_ID_24548158,Human_RBP_ID_26351842,Human_RBP_ID_27826146 Human_Splice_Rec_725744,Human_Splice_Rec_725745,Human_Splice_Rec_725776,Human_Splice_Rec_725777,Human_Splice_Rec_725830,Human_Splice_Rec_725831,Human_Splice_Rec_725894,Human_Splice_Rec_725895,Human_Splice_Rec_725922,Human_Splice_Rec_725923,Human_Splice_Rec_725952,Human_Splice_Rec_725953,Human_Splice_Rec_726015,Human_Splice_Rec_726024,Human_Splice_Rec_726025,Human_Splice_Rec_726038,Human_Splice_Rec_726039,Human_Splice_Rec_726052,Human_Splice_Rec_726053,Human_Splice_Rec_726064,Human_Splice_Rec_726065,Human_Splice_Rec_726080,Human_Splice_Rec_726081 RMVar_hsa_circ_98856,RMVar_hsa_circ_236513,RMVar_hsa_circ_97351,RMVar_hsa_circ_91677,RMVar_hsa_circ_81286,RMVar_hsa_circ_236515,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512,RMVar_hsa_circ_116257,RMVar_hsa_circ_126373,RMVar_hsa_circ_236530,RMVar_hsa_circ_236531,RMVar_hsa_circ_115290,RMVar_hsa_circ_236534,RMVar_hsa_circ_79462,RMVar_hsa_circ_236535 63107 RMVar_ID_63107 Human_SNP_ID_263026601 m1A Human chr5 - 177516379 177516379 177516379 GCGGAGGAAGAGCAGCAGGACAGCGGTAGTGAACCCCGGGGAGATGAGGACGACATCCCGCTAGG GCGGAGGAAGAGCAGCAGGACAGCGGTAGTGACCCCCGGGGAGATGAGGACGACATCCCGCTAGG T G DDX41 Ensembl:ENSG00000183258 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:177516091..177516481 26863196 MeRIP-seq:(Medium) rs1038728566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944854,Human_RBP_ID_9398742,Human_RBP_ID_18471971,Human_RBP_ID_23050460,Human_RBP_ID_24548073,Human_RBP_ID_26351845,Human_RBP_ID_27826148 Human_Splice_Rec_725740,Human_Splice_Rec_725741,Human_Splice_Rec_725772,Human_Splice_Rec_725773,Human_Splice_Rec_725804,Human_Splice_Rec_725805,Human_Splice_Rec_725827,Human_Splice_Rec_725891,Human_Splice_Rec_725918,Human_Splice_Rec_725919,Human_Splice_Rec_725948,Human_Splice_Rec_725949,Human_Splice_Rec_726012,Human_Splice_Rec_726013,Human_Splice_Rec_726021,Human_Splice_Rec_726034,Human_Splice_Rec_726035,Human_Splice_Rec_726048,Human_Splice_Rec_726049,Human_Splice_Rec_726060,Human_Splice_Rec_726061,Human_Splice_Rec_726070,Human_Splice_Rec_726071,Human_Splice_Rec_726077 RMVar_hsa_circ_236513,RMVar_hsa_circ_97351,RMVar_hsa_circ_91677,RMVar_hsa_circ_81286,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512,RMVar_hsa_circ_115290,RMVar_hsa_circ_236534,RMVar_hsa_circ_79462,RMVar_hsa_circ_236535 63108 RMVar_ID_63108 Human_SNP_ID_263026611 m1A Human chr5 - 177516403 177516403 177516403 CTGCAGCGAAGACGCAAGGGAGCTGCGGAGGAAGAGCAGCAGGACAGCGGTAGTGAACCCCGGGG CTGCAGCGAAGACGCAAGGGAGCTGCGGAGGACGAGCAGCAGGACAGCGGTAGTGAACCCCGGGG T G DDX41 Ensembl:ENSG00000183258 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177516089..177516486 26863196 MeRIP-seq:(Medium) rs1261080038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12834,Human_RBP_ID_9398742,Human_RBP_ID_23050460,Human_RBP_ID_24548073,Human_RBP_ID_26351845,Human_RBP_ID_27826148 Human_Splice_Rec_725740,Human_Splice_Rec_725772,Human_Splice_Rec_725804,Human_Splice_Rec_725918,Human_Splice_Rec_725948,Human_Splice_Rec_726012,Human_Splice_Rec_726034,Human_Splice_Rec_726048,Human_Splice_Rec_726060,Human_Splice_Rec_726070 Human_miRNA_ID_2511277,Human_miRNA_ID_3054100 RMVar_hsa_circ_236513,RMVar_hsa_circ_97351,RMVar_hsa_circ_91677,RMVar_hsa_circ_81286,RMVar_hsa_circ_236514,RMVar_hsa_circ_236512,RMVar_hsa_circ_115290,RMVar_hsa_circ_236534,RMVar_hsa_circ_79462,RMVar_hsa_circ_236535 63109 RMVar_ID_63109 Human_SNP_ID_263028865 m1A Human chr5 - 177524544 177524541 177524544 GAAGGGCAAGAGGCAGGGCAGTCAGGCCAAGAAGAGCGAGGCAAGCCCAGCCCCCCGGCCCCCAG GAAGGGCAAGAGGCAGGGCAGTCAGGCCAAGA___GCGAGGCAAGCCCAGCCCCCCGGCCCCCAG CTCT C FAM193B Ensembl:ENSG00000146067 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177524494..177524593 26863196 MeRIP-seq:(Medium) rs761452978 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_26764063 RMVar_hsa_circ_14756,RMVar_hsa_circ_77947,RMVar_hsa_circ_236538,RMVar_hsa_circ_24722 63110 RMVar_ID_63110 Human_SNP_ID_263028867 m1A Human chr5 - 177524557 177524557 177524557 GTGGGAAGCCACAGAAGGGCAAGAGGCAGGGCAGTCAGGCCAAGAAGAGCGAGGCAAGCCCAGCC GTGGGAAGCCACAGAAGGGCAAGAGGCAGGGCTGTCAGGCCAAGAAGAGCGAGGCAAGCCCAGCC T A FAM193B Ensembl:ENSG00000146067 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177524508..177524588 26863196 MeRIP-seq:(Medium) rs1269539431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532126,Human_RBP_ID_26764063 RMVar_hsa_circ_14756,RMVar_hsa_circ_77947,RMVar_hsa_circ_236538,RMVar_hsa_circ_24722 63111 RMVar_ID_63111 Human_SNP_ID_263032001 m1A Human chr5 + 177536578 177536578 177536578 AGCAACAGGGCACTCTGAAGCCTGGGCAGGGAAAGGTGCTGCCGGGGTGGTGGGCAGCAGGTGTG AGCAACAGGGCACTCTGAAGCCTGGGCAGGGAGAGGTGCTGCCGGGGTGGTGGGCAGCAGGTGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177536348..177536750 26863196 MeRIP-seq:(Medium) rs1350808307 Functional Loss SNV dbSNP153 33..33 33 - - - 63112 RMVar_ID_63112 Human_SNP_ID_263036513 m1A Human chr5 + 177553853 177553853 177553853 AGCCGTTCCCGGGGGCAGAGGGAAGAGGCTGCAGTCGTCCAGTCCCAGAGCCCCGAGATGGCCTG AGCCGTTCCCGGGGGCAGAGGGAAGAGGCTGCCGTCGTCCAGTCCCAGAGCCCCGAGATGGCCTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177553788..177553936 26863196 MeRIP-seq:(Medium) rs988890799 Functional Loss SNV dbSNP153 33..33 33 - - - 63113 RMVar_ID_63113 Human_SNP_ID_263036707 m1A Human chr5 - 177554287 177554287 177554287 AGGCGCCGGCGGAGCCCGACCACGACGGCCCCAGGGAGGATGACGAACCCAACCTGGTGCCCGGC AGGCGCCGGCGGAGCCCGACCACGACGGCCCCGGGGAGGATGACGAACCCAACCTGGTGCCCGGC T C FAM193B Ensembl:ENSG00000146067 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177554241..177554443 26863196 MeRIP-seq:(Medium) rs969523841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23050198 Human_Splice_Rec_726097,Human_Splice_Rec_726197,Human_Splice_Rec_726221 63114 RMVar_ID_63114 Human_SNP_ID_263036845 m1A Human chr5 - 177554532 177554509 177554533 CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CATATTGGCTGTTGTCCTGTGAGGGGAGCGG________________________CGGCGGCGGC GCCGCCGCCGCCGCCGCCGCCGCTA G FAM193B Ensembl:ENSG00000146067 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177553497..177554575 26863196 MeRIP-seq:(Medium) rs1561797046 Functional Loss DEL dbSNP153 32..55 33 - - - 63115 RMVar_ID_63115 Human_SNP_ID_263036845 m1A Human chr5 + 177554533 177554509 177554533 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCCCTCACAGGACAACAGCCAATATGG CCGCCGCCG________________________CCGCTCCCCTCACAGGACAACAGCCAATATGG GCCGCCGCCGCCGCCGCCGCCGCTA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:177554278..177554540 26863196 MeRIP-seq:(Medium) rs1561797046 Functional Loss DEL dbSNP153 10..33 33 - - - 63116 RMVar_ID_63116 Human_SNP_ID_263036851 m1A Human chr5 - 177554532 177554523 177554532 CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CATATTGGCTGTTGTCCTGTGAGGGGAGCGGT_________GGCGGCGGCGGCGGCGGCGGCGGC CGCCGCCGCT C FAM193B Ensembl:ENSG00000146067 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177553497..177554575 26863196 MeRIP-seq:(Medium) rs1561797100 Functional Loss DEL dbSNP153 33..41 33 - - - 63117 RMVar_ID_63117 Human_SNP_ID_263036863 m1A Human chr5 - 177554532 177554530 177554533 CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CATATTGGCTGTTGTCCTGTGAGGGGAGCGG___CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCTA G FAM193B Ensembl:ENSG00000146067 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177553497..177554575 26863196 MeRIP-seq:(Medium) rs1244107433 Functional Loss DEL dbSNP153 32..34 33 - - - 63118 RMVar_ID_63118 Human_SNP_ID_263036863 m1A Human chr5 + 177554533 177554530 177554533 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCCCTCACAGGACAACAGCCAATATGG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCG___CCGCTCCCCTCACAGGACAACAGCCAATATGG GCTA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:177554278..177554540 26863196 MeRIP-seq:(Medium) rs1244107433 Functional Loss DEL dbSNP153 31..33 33 - - - 63119 RMVar_ID_63119 Human_SNP_ID_263036864 m1A Human chr5 - 177554532 177554532 177554532 CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C FAM193B Ensembl:ENSG00000146067 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177553497..177554575 26863196 MeRIP-seq:(Medium) rs1158273791 Functional Loss SNV dbSNP153 33..33 33 - - - 63120 RMVar_ID_63120 Human_SNP_ID_263036865 m1A Human chr5 + 177554533 177554533 177554533 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCCCTCACAGGACAACAGCCAATATGG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTGCCGCTCCCCTCACAGGACAACAGCCAATATGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:177554278..177554540 26863196 MeRIP-seq:(Medium) rs1391139143 Functional Loss SNV dbSNP153 33..33 33 - - - 63121 RMVar_ID_63121 Human_SNP_ID_263046351 m1A Human chr5 + 177592215 177592215 177592215 CCGGCTGCGGCTGCGCAGGCAGGTGGAGCAAGATGGCTGTGGAGCTGGGCGTGCTGCTCGTCCGG CCGGCTGCGGCTGCGCAGGCAGGTGGAGCAAGGTGGCTGTGGAGCTGGGCGTGCTGCTCGTCCGG A G TMED9 Ensembl:ENSG00000184840 Protein coding start codon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1302669076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250979,Human_RBP_ID_1651479,Human_RBP_ID_4825343,Human_RBP_ID_5326664,Human_RBP_ID_5427170,Human_RBP_ID_5449689,Human_RBP_ID_5476560,Human_RBP_ID_7421748,Human_RBP_ID_8611563,Human_RBP_ID_8888672,Human_RBP_ID_9335493,Human_RBP_ID_18839343,Human_RBP_ID_21215742,Human_RBP_ID_22459053,Human_RBP_ID_24099324,Human_RBP_ID_26350578,Human_RBP_ID_27079316,Human_RBP_ID_27160447,Human_RBP_ID_27335150 RMVar_hsa_circ_96167,RMVar_hsa_circ_112447,RMVar_hsa_circ_236545,RMVar_hsa_circ_236546 63122 RMVar_ID_63122 Human_SNP_ID_263046422 m1A Human chr5 - 177592288 177592288 177592288 TTCCGCGCGTCGCCAGCCACAGCACCAGCAGGAGGGTCCGCATCACTCTACCCAGCCCGGTTCCG TTCCGCGCGTCGCCAGCCACAGCACCAGCAGGCGGGTCCGCATCACTCTACCCAGCCCGGTTCCG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:177592176..177592400 26863410 MeRIP-seq:(Medium) rs1561809035 Functional Loss SNV dbSNP153 33..33 33 - - - 63123 RMVar_ID_63123 Human_SNP_ID_263046459 m1A Human chr5 + 177592343 177592343 177592343 ACGCGCGGAAGCGCGCTCTACTTTCACATCGGAGAGACGGAGAAGAAGTGCTTTATTGAGGAGAT ACGCGCGGAAGCGCGCTCTACTTTCACATCGGGGAGACGGAGAAGAAGTGCTTTATTGAGGAGAT A G TMED9 Ensembl:ENSG00000184840 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177592226..177592400 26863196 MeRIP-seq:(Medium) rs776261361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76919,Human_RBP_ID_639070,Human_RBP_ID_1040839,Human_RBP_ID_1651482,Human_RBP_ID_1993129,Human_RBP_ID_4847248,Human_RBP_ID_7421752,Human_RBP_ID_8611567,Human_RBP_ID_9335494,Human_RBP_ID_15400896,Human_RBP_ID_18839345,Human_RBP_ID_23116225,Human_RBP_ID_24099327 Human_Splice_Rec_726227,Human_Splice_Rec_726237 Human_miRNA_ID_3035023 RMVar_hsa_circ_96167,RMVar_hsa_circ_112447,RMVar_hsa_circ_236545,RMVar_hsa_circ_236546 63124 RMVar_ID_63124 Human_SNP_ID_263046468 m1A Human chr5 + 177592351 177592351 177592351 AAGCGCGCTCTACTTTCACATCGGAGAGACGGAGAAGAAGTGCTTTATTGAGGAGATCCCGGACG AAGCGCGCTCTACTTTCACATCGGAGAGACGGCGAAGAAGTGCTTTATTGAGGAGATCCCGGACG A C TMED9 Ensembl:ENSG00000184840 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177592301..177592375 26863196 MeRIP-seq:(Medium) rs1236042698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76919,Human_RBP_ID_639070,Human_RBP_ID_1651482,Human_RBP_ID_1993129,Human_RBP_ID_4847248,Human_RBP_ID_7421752,Human_RBP_ID_8611567,Human_RBP_ID_9335495,Human_RBP_ID_9398747,Human_RBP_ID_15400896,Human_RBP_ID_18839345,Human_RBP_ID_23116225,Human_RBP_ID_24099327 Human_Splice_Rec_726227,Human_Splice_Rec_726237 Human_miRNA_ID_3035023 RMVar_hsa_circ_96167,RMVar_hsa_circ_112447,RMVar_hsa_circ_236545,RMVar_hsa_circ_236546 63125 RMVar_ID_63125 Human_SNP_ID_263046921 m1A Human chr5 - 177593693 177593693 177593693 AGATCTGGTGCTCACCAGGGGTATGGGAAGTGAAAGTGAACCTGCCCTCGGAGCCATACTGCCGG AGATCTGGTGCTCACCAGGGGTATGGGAAGTGGAAGTGAACCTGCCCTCGGAGCCATACTGCCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177593649..177593775 32194978 MeRIP-seq:(Medium) rs770235160 Functional Loss SNV dbSNP153 33..33 33 - - - 63126 RMVar_ID_63126 Human_SNP_ID_263048778 m1A Human chr5 - 177600214 177600214 177600214 GGGCAGCTGCGCCGCTTTCCTCCGCGAGGGGAACATCGTGCGGAGAGGCGGCGGCGCATGGGGCA GGGCAGCTGCGCCGCTTTCCTCCGCGAGGGGATCATCGTGCGGAGAGGCGGCGGCGCATGGGGCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177600168..177600433 26863196 MeRIP-seq:(Medium) rs1160171646 Functional Loss SNV dbSNP153 33..33 33 - - - 63127 RMVar_ID_63127 Human_SNP_ID_263048790 m1A Human chr5 + 177600230 177600230 177600230 GCCTCTCCGCACGATGTTCCCCTCGCGGAGGAAAGCGGCGCAGCTGCCCTGGGAGGACGGCAGGT GCCTCTCCGCACGATGTTCCCCTCGCGGAGGAGAGCGGCGCAGCTGCCCTGGGAGGACGGCAGGT A G B4GALT7 Ensembl:ENSG00000027847 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:177600179..177600291;chr5:177600179..177600329 26863196 MeRIP-seq:(Medium) rs1370799068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250568,Human_RBP_ID_4825427 Human_Splice_Rec_726257,Human_Splice_Rec_726261,Human_Splice_Rec_726271,Human_Splice_Rec_726281,Human_Splice_Rec_726287 63128 RMVar_ID_63128 Human_SNP_ID_263048834 m1A Human chr5 + 177600341 177600341 177600341 CTTCTCGGCCGCCGGCGGAATCTGGGAACCCGAGGCCATCACGTCTCCATGTCTGCGGGTTTCTG CTTCTCGGCCGCCGGCGGAATCTGGGAACCCGGGGCCATCACGTCTCCATGTCTGCGGGTTTCTG A G B4GALT7 Ensembl:ENSG00000027847 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177600238..177600365 26863196 MeRIP-seq:(Medium) rs1050030873 Functional Loss SNV dbSNP153 33..33 33 - - - 63129 RMVar_ID_63129 Human_SNP_ID_263048835 m1A Human chr5 + 177600341 177600341 177600341 CTTCTCGGCCGCCGGCGGAATCTGGGAACCCGAGGCCATCACGTCTCCATGTCTGCGGGTTTCTG CTTCTCGGCCGCCGGCGGAATCTGGGAACCCGTGGCCATCACGTCTCCATGTCTGCGGGTTTCTG A T B4GALT7 Ensembl:ENSG00000027847 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:177600238..177600365 26863196 MeRIP-seq:(Medium) rs1050030873 Functional Loss SNV dbSNP153 33..33 33 - - - 63130 RMVar_ID_63130 Human_SNP_ID_263049401 m1A Human chr5 + 177602710 177602710 177602710 CCCAACATGAGAACATGGGGCGAAGGCTTGGGAGCACCTGGAGTTGGGGCCAGGTCATGGAGGGC CCCAACATGAGAACATGGGGCGAAGGCTTGGGGGCACCTGGAGTTGGGGCCAGGTCATGGAGGGC A G B4GALT7 Ensembl:ENSG00000027847 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177602695..177602803 26863196 MeRIP-seq:(Medium) rs1045176567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7421804,Human_RBP_ID_15401061 63131 RMVar_ID_63131 Human_SNP_ID_263049871 m1A Human chr5 + 177604373 177604373 177604373 TCCCCGTGCCTGCCCCCCAGAGCCGCCCCCTGAGCACTGGGAAGAAGACGCATCCTGGGGCCCCC TCCCCGTGCCTGCCCCCCAGAGCCGCCCCCTGGGCACTGGGAAGAAGACGCATCCTGGGGCCCCC A G B4GALT7 Ensembl:ENSG00000027847 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177604324..177604424 32194978 MeRIP-seq:(Medium) rs1483839796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19016269 Human_Splice_Rec_726258 63132 RMVar_ID_63132 Human_SNP_ID_263053690 m1A Human chr5 - 177618096 177618093 177618097 GGGAAGGAGGGAAAGAAAAAGGAAGGAAAGAAAGAGAAAGAGAAAACACTATAACAGAGATGATG GGGAAGGAGGGAAAGAAAAAGGAAGGAAAGA____GAAAGAGAAAACACTATAACAGAGATGATG CTCTT C lnc-FAM153A-3 RNACentral:URS00008B9384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177618045..177618118 26863196 MeRIP-seq:(Medium) rs1467988839 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_2920041,Human_RBP_ID_17069765,Human_RBP_ID_23051486,Human_RBP_ID_25939935 63133 RMVar_ID_63133 Human_SNP_ID_263053691 m1A Human chr5 - 177618096 177618096 177618096 GGGAAGGAGGGAAAGAAAAAGGAAGGAAAGAAAGAGAAAGAGAAAACACTATAACAGAGATGATG GGGAAGGAGGGAAAGAAAAAGGAAGGAAAGAAGGAGAAAGAGAAAACACTATAACAGAGATGATG T C lnc-FAM153A-3 RNACentral:URS00008B9384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177618045..177618118 26863196 MeRIP-seq:(Medium) rs1258695604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2920041,Human_RBP_ID_17069765,Human_RBP_ID_23051486,Human_RBP_ID_25939935 63134 RMVar_ID_63134 Human_SNP_ID_263109085 m1A Human chr5 + 177882471 177882471 177882471 CCCATGGGGAAGTACTTTGCCACAGGAAGTGCAGATGCTTTGGTCAGCCTCTGGGATGTGGATGA CCCATGGGGAAGTACTTTGCCACAGGAAGTGCCGATGCTTTGGTCAGCCTCTGGGATGTGGATGA A C AC106795.1 Ensembl:ENSG00000170089 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11552883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17415848 Human_Splice_Rec_726711,Human_Splice_Rec_726737,Human_Splice_Rec_726747,Human_Splice_Rec_726763,Human_Splice_Rec_726769,Human_Splice_Rec_726773,Human_Splice_Rec_726777,Human_Splice_Rec_726779 Human_miRNA_ID_1858155,Human_miRNA_ID_1880932,Human_miRNA_ID_1906932,Human_miRNA_ID_2430591,Human_miRNA_ID_2713339,Human_miRNA_ID_3049319 RMVar_hsa_circ_39670,RMVar_hsa_circ_116902,RMVar_hsa_circ_236558,RMVar_hsa_circ_44962,RMVar_hsa_circ_47623 63135 RMVar_ID_63135 Human_SNP_ID_263109086 m1A Human chr5 + 177882471 177882471 177882471 CCCATGGGGAAGTACTTTGCCACAGGAAGTGCAGATGCTTTGGTCAGCCTCTGGGATGTGGATGA CCCATGGGGAAGTACTTTGCCACAGGAAGTGCGGATGCTTTGGTCAGCCTCTGGGATGTGGATGA A G AC106795.1 Ensembl:ENSG00000170089 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11552883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17415848 Human_Splice_Rec_726711,Human_Splice_Rec_726737,Human_Splice_Rec_726747,Human_Splice_Rec_726763,Human_Splice_Rec_726769,Human_Splice_Rec_726773,Human_Splice_Rec_726777,Human_Splice_Rec_726779 Human_miRNA_ID_1858155,Human_miRNA_ID_1880932,Human_miRNA_ID_1906932,Human_miRNA_ID_2430591,Human_miRNA_ID_2713339,Human_miRNA_ID_3049319 RMVar_hsa_circ_39670,RMVar_hsa_circ_116902,RMVar_hsa_circ_236558,RMVar_hsa_circ_44962,RMVar_hsa_circ_47623 63136 RMVar_ID_63136 Human_SNP_ID_263119266 m1A Human chr5 - 177939321 177939321 177939321 CAGGACGCGGTAGCAGCGGGGCTCCACTAAGCAGGGATAGGAGCGTGGGGCGGTAGCTGCCAGAC CAGGACGCGGTAGCAGCGGGGCTCCACTAAGCGGGGATAGGAGCGTGGGGCGGTAGCTGCCAGAC T C RF00017-4673,RF00017-4525 RNACentral:URS000091B0E9,RNACentral:URS00009368C0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177939319..177939457 26863196 MeRIP-seq:(Medium) rs1336000701 Functional Loss SNV dbSNP153 33..33 33 - - - 63137 RMVar_ID_63137 Human_SNP_ID_263120879 m1A Human chr5 - 177945197 177945197 177945197 CAGCACCATCCATGCCTTTTGATGCCCGGGCCACCCGCCCTGCCCCACCTGTCCTCAGCACAGCA CAGCACCATCCATGCCTTTTGATGCCCGGGCCCCCCGCCCTGCCCCACCTGTCCTCAGCACAGCA T G RF00017-4673,RF00017-4525 RNACentral:URS000091B0E9,RNACentral:URS00009368C0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:177945193..177945313 26863196 MeRIP-seq:(Medium) rs1209445391 Functional Loss SNV dbSNP153 33..33 33 - - - 63138 RMVar_ID_63138 Human_SNP_ID_263126286 m1A Human chr5 - 177961336 177961336 177961336 CACGCTCCCTCTTCAGTGTCACCACGGCCATCATTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC CACGCTCCCTCTTCAGTGTCACCACGGCCATCGTTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC T C RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0 SRP RNA,lincRNA,lincRNA,SRP RNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961248..177961465 26863196 MeRIP-seq:(Medium) rs10040126 Functional Loss SNV dbSNP153 33..33 33 - - - 63139 RMVar_ID_63139 Human_SNP_ID_263126287 m1A Human chr5 - 177961336 177961336 177961336 CACGCTCCCTCTTCAGTGTCACCACGGCCATCATTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC CACGCTCCCTCTTCAGTGTCACCACGGCCATCCTTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC T G RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0 SRP RNA,lincRNA,lincRNA,SRP RNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961248..177961465 26863196 MeRIP-seq:(Medium) rs10040126 Functional Loss SNV dbSNP153 33..33 33 - - - 63140 RMVar_ID_63140 Human_SNP_ID_263126376 m1A Human chr5 - 177961655 177961655 177961655 GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAATGTCAGCCATGGCCATCGTTCCCTCTGCCACG GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAGTGTCAGCCATGGCCATCGTTCCCTCTGCCACG T C RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525,lnc-PROP1-2:3 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0,RNACentral:URS00008B2D92 SRP RNA,lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961649..177961740 26863196 MeRIP-seq:(Medium) rs11743951 Functional Loss SNV dbSNP153 33..33 33 - - - 63141 RMVar_ID_63141 Human_SNP_ID_263126377 m1A Human chr5 - 177961655 177961655 177961655 GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAATGTCAGCCATGGCCATCGTTCCCTCTGCCACG GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCACTGTCAGCCATGGCCATCGTTCCCTCTGCCACG T G RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525,lnc-PROP1-2:3 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0,RNACentral:URS00008B2D92 SRP RNA,lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961649..177961740 26863196 MeRIP-seq:(Medium) rs11743951 Functional Loss SNV dbSNP153 33..33 33 - - - 63142 RMVar_ID_63142 Human_SNP_ID_263158178 m1A Human chr5 - 178078211 178078211 178078211 CTGCTGCTGGTGTAAGCGAAGAACTTAGGATGAAATTGATTGGTGGGAATGGCAGGAGAAGATTT CTGCTGCTGGTGTAAGCGAAGAACTTAGGATGCAATTGATTGGTGGGAATGGCAGGAGAAGATTT T G MG828692 RNACentral:URS0000E18587 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178078172..178078257 26863196 MeRIP-seq:(Medium) rs1362641374 Functional Loss SNV dbSNP153 33..33 33 - - - 63143 RMVar_ID_63143 Human_SNP_ID_263167995 m1A Human chr5 - 178113600 178113600 178113600 GCCGGGAAAACGCGGGCGGGCGCCGGCGCCGGAGCCGGATTGGCGAGGGAGGGACGCGCTCCGCG GCCGGGAAAACGCGGGCGGGCGCCGGCGCCGGCGCCGGATTGGCGAGGGAGGGACGCGCTCCGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178113562..178113676 26863196 MeRIP-seq:(Medium) rs1350296964 Functional Loss SNV dbSNP153 33..33 33 - - - 63144 RMVar_ID_63144 Human_SNP_ID_263169754 m1A Human chr5 - 178119669 178119669 178119669 GGGAGCCCCGAGACCCGGCAAGTGCCGCCCGCAGCTCTTCAGGGGAGAAGTCCTGCCGTTCCAAC GGGAGCCCCGAGACCCGGCAAGTGCCGCCCGCGGCTCTTCAGGGGAGAAGTCCTGCCGTTCCAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178119622..178119786 26863196 MeRIP-seq:(Medium) rs543249506 Functional Loss SNV dbSNP153 33..33 33 - - - 63145 RMVar_ID_63145 Human_SNP_ID_263169764 m1A Human chr5 - 178119691 178119691 178119691 CGGAGGAGCCCATCAGGCTGGCGGGAGCCCCGAGACCCGGCAAGTGCCGCCCGCAGCTCTTCAGG CGGAGGAGCCCATCAGGCTGGCGGGAGCCCCGGGACCCGGCAAGTGCCGCCCGCAGCTCTTCAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178119644..178119784 26863196 MeRIP-seq:(Medium) rs769398073 Functional Loss SNV dbSNP153 33..33 33 - - - 63146 RMVar_ID_63146 Human_SNP_ID_263170092 m1A Human chr5 + 178120454 178120454 178120454 CCAGTGGGGGTAGTTTTGGTCGCAGTCCTGGTACTGGCCCTAGCCCCTTCAGCTCCTCCCTTGGC CCAGTGGGGGTAGTTTTGGTCGCAGTCCTGGTCCTGGCCCTAGCCCCTTCAGCTCCTCCCTTGGC A C N4BP3 Ensembl:ENSG00000145911 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178120403..178120599 26863196 MeRIP-seq:(Medium) rs978309349 Functional Loss SNV dbSNP153 33..33 33 - - - 63147 RMVar_ID_63147 Human_SNP_ID_263170399 m1A Human chr5 - 178121201 178121201 178121201 GCTCCTGCTGAGCCATAAACAGCTGCAGCTGGAGGTTGCGCTCGCTGCGCTCAGCCTTCTGGGTC GCTCCTGCTGAGCCATAAACAGCTGCAGCTGGGGGTTGCGCTCGCTGCGCTCAGCCTTCTGGGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178121151..178121326 26863196 MeRIP-seq:(Medium) rs1323808594 Functional Loss SNV dbSNP153 33..33 33 - - - 63148 RMVar_ID_63148 Human_SNP_ID_263170618 m1A Human chr5 - 178121641 178121641 178121641 TCCCGAGGGGCCTGCTCCTGCAGGCTGCGCACAGCCTCGCGCAGCCGGACCAGCTCTGCGTCCTG TCCCGAGGGGCCTGCTCCTGCAGGCTGCGCACTGCCTCGCGCAGCCGGACCAGCTCTGCGTCCTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178121591..178121680 26863196 MeRIP-seq:(Medium) rs1013226900 Functional Loss SNV dbSNP153 33..33 33 - - - 63149 RMVar_ID_63149 Human_SNP_ID_263170619 m1A Human chr5 - 178121641 178121641 178121641 TCCCGAGGGGCCTGCTCCTGCAGGCTGCGCACAGCCTCGCGCAGCCGGACCAGCTCTGCGTCCTG TCCCGAGGGGCCTGCTCCTGCAGGCTGCGCACGGCCTCGCGCAGCCGGACCAGCTCTGCGTCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178121591..178121680 26863196 MeRIP-seq:(Medium) rs1013226900 Functional Loss SNV dbSNP153 33..33 33 - - - 63150 RMVar_ID_63150 Human_SNP_ID_263170697 m1A Human chr5 + 178121790 178121790 178121790 TGCTGAGCAGCTGCGGGCTGAGCTGCTGCAGGAGCGACTTCGGGGCCAGGAGCAGGCGCTGCGCT TGCTGAGCAGCTGCGGGCTGAGCTGCTGCAGGCGCGACTTCGGGGCCAGGAGCAGGCGCTGCGCT A C N4BP3 Ensembl:ENSG00000145911 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178121742..178121953 26863196 MeRIP-seq:(Medium) rs1281927079 Functional Loss SNV dbSNP153 33..33 33 - - - 63151 RMVar_ID_63151 Human_SNP_ID_263170858 m1A Human chr5 - 178122144 178122144 178122144 CTGCCAAGGCACCCTACCCAGCCCACGGCCCCACTGGATCCCTCCTCTCCTTGCGCCTCCCCAGC CTGCCAAGGCACCCTACCCAGCCCACGGCCCCGCTGGATCCCTCCTCTCCTTGCGCCTCCCCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178122093..178122294 26863196 MeRIP-seq:(Medium) rs1296936331 Functional Loss SNV dbSNP153 33..33 33 - - - 63152 RMVar_ID_63152 Human_SNP_ID_263171701 m1A Human chr5 + 178125274 178125273 178125275 GCTTACCTGTGGGTGGGGGAGGGAGACCACACATGTCAGAGGTAGTGAAGGCCGCTCCAAATAGT GCTTACCTGTGGGTGGGGGAGGGAGACCACAC__GTCAGAGGTAGTGAAGGCCGCTCCAAATAGT CAT C N4BP3 Ensembl:ENSG00000145911 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178125264..178125428 26863196 MeRIP-seq:(Medium) rs1026365949 Functional Loss DEL dbSNP153 33..34 33 - - - 63153 RMVar_ID_63153 Human_SNP_ID_263173484 m1A Human chr5 + 178131083 178131083 178131083 CGAGGTGAGAGCGGGCGGGCTTGGGAGCCGGCAGGTGCGGGCCGAGGGCGGGCACAGCGGCCGGC CGAGGTGAGAGCGGGCGGGCTTGGGAGCCGGCGGGTGCGGGCCGAGGGCGGGCACAGCGGCCGGC A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:178131026..178131189 26863196 MeRIP-seq:(Medium) rs1470146037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250779,Human_RBP_ID_4846214,Human_RBP_ID_9335501,Human_RBP_ID_18425059,Human_RBP_ID_19125072 63154 RMVar_ID_63154 Human_SNP_ID_263173506 m1A Human chr5 + 178131138 178131138 178131138 AGCGGCCGGCGGAGCTGAGGCGCGCGGCGGGGAAAGCTCGGCCGGCCTCCCGGGCCCCAGCCTTC AGCGGCCGGCGGAGCTGAGGCGCGCGGCGGGGGAAGCTCGGCCGGCCTCCCGGGCCCCAGCCTTC A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:178131026..178131200 26863410 MeRIP-seq:(Medium) rs966910887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250779,Human_RBP_ID_4825537,Human_RBP_ID_5427177,Human_RBP_ID_9335501,Human_RBP_ID_18425059,Human_RBP_ID_19125072 63155 RMVar_ID_63155 Human_SNP_ID_263173682 m1A Human chr5 - 178131657 178131657 178131657 ATGTCCCGTCCTCAGAGATGCTCTGCTAGACCACAGTATCTAATACTGACCCCTCCGCCCCACCC ATGTCCCGTCCTCAGAGATGCTCTGCTAGACCGCAGTATCTAATACTGACCCCTCCGCCCCACCC T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178131652..178131991 26863196 MeRIP-seq:(Medium) rs1295866303 Functional Loss SNV dbSNP153 33..33 33 - - - 63156 RMVar_ID_63156 Human_SNP_ID_263178243 m1A Human chr5 + 178148327 178148327 178148327 GCGTTTGACTTAGTAGCAACCGACAGAGTGGCAAGGGATTTGGTCTTCAGCAGTAGACATCCTTC GCGTTTGACTTAGTAGCAACCGACAGAGTGGCGAGGGATTTGGTCTTCAGCAGTAGACATCCTTC A G RMND5B Ensembl:ENSG00000145916 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:178148279..178148479 32194978 MeRIP-seq:(Medium) rs913689875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639186,Human_RBP_ID_1651570,Human_RBP_ID_1993195,Human_RBP_ID_3766571,Human_RBP_ID_9341499,Human_RBP_ID_15402517 Human_miRNA_ID_445509,Human_miRNA_ID_545555,Human_miRNA_ID_580792,Human_miRNA_ID_2141983,Human_miRNA_ID_3045789 RMVar_hsa_circ_93045,RMVar_hsa_circ_236561 63157 RMVar_ID_63157 Human_SNP_ID_263178573 m1A Human chr5 - 178149598 178149598 178149598 ACACTGACGGCATCTTCCCAGTTCCCCAAGGCACGCCTTCTTCCCAGGCAGCTCTAACAGCCCTT ACACTGACGGCATCTTCCCAGTTCCCCAAGGCTCGCCTTCTTCCCAGGCAGCTCTAACAGCCCTT T A NHP2 Ensembl:ENSG00000145912 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:178149556..178149655 32194978 MeRIP-seq:(Medium) rs1348248802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639203,Human_RBP_ID_4825616,Human_RBP_ID_8267482,Human_RBP_ID_9175031,Human_RBP_ID_26826899,Human_RBP_ID_27514604 63158 RMVar_ID_63158 Human_SNP_ID_263179829 m1A Human chr5 - 178153667 178153667 178153667 CTCGCCGCCTCACGCGGAAGCTCTACAAATGCATCAAGAAAGGTGAGGCGGACGGCGGCGTGGCC CTCGCCGCCTCACGCGGAAGCTCTACAAATGCGTCAAGAAAGGTGAGGCGGACGGCGGCGTGGCC T C NHP2 Ensembl:ENSG00000145912 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:178153501..178153870 32194978 MeRIP-seq:(Medium) rs775477260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4853548,Human_RBP_ID_22615546 Human_Splice_Rec_727949,Human_Splice_Rec_727955,Human_Splice_Rec_727961,Human_Splice_Rec_727967,Human_Splice_Rec_727971 63159 RMVar_ID_63159 Human_SNP_ID_263179861 m1A Human chr5 - 178153744 178153744 178153744 GGCGGAGGCGTGTTCCGGGGAGCGCACCTACCAGGAGCTGCTGGTCAACCAGAACCCCATCGCGC GGCGGAGGCGTGTTCCGGGGAGCGCACCTACCTGGAGCTGCTGGTCAACCAGAACCCCATCGCGC T A NHP2 Ensembl:ENSG00000145912 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:178153599..178153875 26863196 MeRIP-seq:(Medium) rs11550513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250777,Human_RBP_ID_639232,Human_RBP_ID_4825633,Human_RBP_ID_9335503,Human_RBP_ID_9398752,Human_RBP_ID_22459424 Human_Splice_Rec_727949,Human_Splice_Rec_727955,Human_Splice_Rec_727961,Human_Splice_Rec_727967,Human_Splice_Rec_727971 63160 RMVar_ID_63160 Human_SNP_ID_263179886 m1A Human chr5 - 178153777 178153777 178153777 AATAAAGGCAGATCCCGACGGGCCCGAGGCTCAGGCGGAGGCGTGTTCCGGGGAGCGCACCTACC AATAAAGGCAGATCCCGACGGGCCCGAGGCTCGGGCGGAGGCGTGTTCCGGGGAGCGCACCTACC T C NHP2 Ensembl:ENSG00000145912 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:178153676..178153875 26863410 MeRIP-seq:(Medium) rs1561645423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250777,Human_RBP_ID_639232,Human_RBP_ID_4846218,Human_RBP_ID_7422135,Human_RBP_ID_8611701,Human_RBP_ID_9335503,Human_RBP_ID_9398752,Human_RBP_ID_18195180,Human_RBP_ID_18425333,Human_RBP_ID_22459424,Human_RBP_ID_24099567,Human_RBP_ID_26826906,Human_RBP_ID_27079509,Human_RBP_ID_27335247,Human_RBP_ID_27514613 63161 RMVar_ID_63161 Human_SNP_ID_263179899 m1A Human chr5 - 178153804 178153804 178153804 GGTTTCAGCGGCCGCTGCGATGACCAAAATAAAGGCAGATCCCGACGGGCCCGAGGCTCAGGCGG GGTTTCAGCGGCCGCTGCGATGACCAAAATAATGGCAGATCCCGACGGGCCCGAGGCTCAGGCGG T A NHP2 Ensembl:ENSG00000145912 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs898669777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639232,Human_RBP_ID_4846218,Human_RBP_ID_9398752,Human_RBP_ID_18195180,Human_RBP_ID_18425333,Human_RBP_ID_22459424,Human_RBP_ID_24099567,Human_RBP_ID_26826906 63162 RMVar_ID_63162 Human_SNP_ID_263182602 m1A Human chr5 + 178163839 178163832 178163840 GGCAGGCTGGGAAAGAAAATTTTAAAAAAGGAAGGAAGGAAGGGAGGGAAAAGAGAAAAAAGAAA GGCAGGCTGGGAAAGAAAATTTTAAA________GAAGGAAGGGAGGGAAAAGAGAAAAAAGAAA AAAAGGAAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178163836..178163967 26863196 MeRIP-seq:(Medium) rs1461724106 Functional Loss DEL dbSNP153 27..34 33 - - - 63163 RMVar_ID_63163 Human_SNP_ID_263182628 m1A Human chr5 + 178163874 178163874 178163874 AAGGAAGGGAGGGAAAAGAGAAAAAAGAAAAGAAAGGAAGACCAATGTAGAGGGTGAGGCAGGGC AAGGAAGGGAGGGAAAAGAGAAAAAAGAAAAGGAAGGAAGACCAATGTAGAGGGTGAGGCAGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:178163761..178163985 26863196 MeRIP-seq:(Medium) rs1312149811 Functional Loss SNV dbSNP153 33..33 33 - - - 63164 RMVar_ID_63164 Human_SNP_ID_263193987 m1A Human chr5 + 178205019 178205019 178205019 GAATCAGAACGGCGCCGAGGGCGACCAGATCAACGCCAGCAAGAACGAGGAGGACGCGGGGTAGG GAATCAGAACGGCGCCGAGGGCGACCAGATCAGCGCCAGCAAGAACGAGGAGGACGCGGGGTAGG A G HNRNPAB Ensembl:ENSG00000197451 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:178204526..178205050 26863196 MeRIP-seq:(Medium) rs993789990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77026,Human_RBP_ID_1651597,Human_RBP_ID_1993204,Human_RBP_ID_4825652,Human_RBP_ID_7422189,Human_RBP_ID_22459063,Human_RBP_ID_23050468 Human_Splice_Rec_727975,Human_Splice_Rec_727989,Human_Splice_Rec_728003,Human_Splice_Rec_728015,Human_Splice_Rec_728027,Human_Splice_Rec_728037,Human_Splice_Rec_728047 RMVar_hsa_circ_236562,RMVar_hsa_circ_115516,RMVar_hsa_circ_236564,RMVar_hsa_circ_359670,RMVar_hsa_circ_371406,RMVar_hsa_circ_236563 63165 RMVar_ID_63165 Human_SNP_ID_263194316 m1A Human chr5 + 178205743 178205743 178205743 TTTCTAAGGTGCTCCTTGCAGACTCTAAGGGTAGCTGTAGACTTCGTGAGAACTTTGCCAGGGCC TTTCTAAGGTGCTCCTTGCAGACTCTAAGGGTGGCTGTAGACTTCGTGAGAACTTTGCCAGGGCC A G HNRNPAB Ensembl:ENSG00000197451 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:178205729..178205925 26863196 MeRIP-seq:(Medium) rs977429113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15402822 RMVar_hsa_circ_236564,RMVar_hsa_circ_371406 63166 RMVar_ID_63166 Human_SNP_ID_263194329 m1A Human chr5 + 178205788 178205788 178205788 GTGAGAACTTTGCCAGGGCCAGTCCTTTCCAAAATCACAGCTTGCTTACAAGACTTGTTGCCGTG GTGAGAACTTTGCCAGGGCCAGTCCTTTCCAAGATCACAGCTTGCTTACAAGACTTGTTGCCGTG A G HNRNPAB Ensembl:ENSG00000197451 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:178205786..178205951 26863196 MeRIP-seq:(Medium) rs916090280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8136721,Human_RBP_ID_15402826 RMVar_hsa_circ_236564,RMVar_hsa_circ_371406 63167 RMVar_ID_63167 Human_SNP_ID_263194335 m1A Human chr5 - 178205798 178205798 178205798 GGGTGAGACACACGGCAACAAGTCTTGTAAGCAAGCTGTGATTTTGGAAAGGACTGGCCCTGGCA GGGTGAGACACACGGCAACAAGTCTTGTAAGCGAGCTGTGATTTTGGAAAGGACTGGCCCTGGCA T C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178205796..178206010 26863196 MeRIP-seq:(Medium) rs1271806361 Functional Loss SNV dbSNP153 33..33 33 - - - 63168 RMVar_ID_63168 Human_SNP_ID_263194354 m1A Human chr5 + 178205827 178205827 178205827 GCTTGCTTACAAGACTTGTTGCCGTGTGTCTCACCCTACCATTTCAGAAAAATGTTCGTTGGTGG GCTTGCTTACAAGACTTGTTGCCGTGTGTCTCGCCCTACCATTTCAGAAAAATGTTCGTTGGTGG A G HNRNPAB Ensembl:ENSG00000197451 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:178205826..178205900 26863196 MeRIP-seq:(Medium) rs761602836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944875,Human_RBP_ID_8136721 RMVar_hsa_circ_236564,RMVar_hsa_circ_371406 63169 RMVar_ID_63169 Human_SNP_ID_263194845 m1A Human chr5 + 178207164 178207164 178207164 CAAAAGACGAGGTTTTGTGTTTATCACCTTTAAAGAAGAAGAACCCGTGAAGAAGGTTCTGGAGA CAAAAGACGAGGTTTTGTGTTTATCACCTTTACAGAAGAAGAACCCGTGAAGAAGGTTCTGGAGA A C HNRNPAB Ensembl:ENSG00000197451 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs539223730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77032,Human_RBP_ID_639244,Human_RBP_ID_1040878,Human_RBP_ID_1651616,Human_RBP_ID_1993210,Human_RBP_ID_2920207,Human_RBP_ID_4825672,Human_RBP_ID_7422211,Human_RBP_ID_8611723,Human_RBP_ID_9175044,Human_RBP_ID_9398758,Human_RBP_ID_17707786,Human_RBP_ID_18357130,Human_RBP_ID_22299272,Human_RBP_ID_22827956,Human_RBP_ID_23051514,Human_RBP_ID_24548160,Human_RBP_ID_25939992,Human_RBP_ID_26350580,Human_RBP_ID_27079542,Human_RBP_ID_27335270,Human_RBP_ID_27738937 Human_Splice_Rec_727980,Human_Splice_Rec_727981,Human_Splice_Rec_727994,Human_Splice_Rec_727995,Human_Splice_Rec_728008,Human_Splice_Rec_728009,Human_Splice_Rec_728020,Human_Splice_Rec_728021,Human_Splice_Rec_728032,Human_Splice_Rec_728033,Human_Splice_Rec_728042,Human_Splice_Rec_728043,Human_Splice_Rec_728052,Human_Splice_Rec_728053 RMVar_hsa_circ_59048,RMVar_hsa_circ_236564,RMVar_hsa_circ_371406,RMVar_hsa_circ_18259,RMVar_hsa_circ_367308 63170 RMVar_ID_63170 Human_SNP_ID_263194857 m1A Human chr5 + 178207200 178207200 178207200 AGAAGAACCCGTGAAGAAGGTTCTGGAGAAAAAGTTCCATACTGTCAGTGGAAGCAAGGTAAGGT AGAAGAACCCGTGAAGAAGGTTCTGGAGAAAAGGTTCCATACTGTCAGTGGAAGCAAGGTAAGGT A G HNRNPAB Ensembl:ENSG00000197451 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:178207126..178207250 32194978 MeRIP-seq:(Medium) rs761979927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1040879,Human_RBP_ID_1651616,Human_RBP_ID_1993211,Human_RBP_ID_3766593,Human_RBP_ID_7422214,Human_RBP_ID_9398758,Human_RBP_ID_15402882,Human_RBP_ID_18839500,Human_RBP_ID_22512109,Human_RBP_ID_24099608,Human_RBP_ID_24548160,Human_RBP_ID_26350580 Human_Splice_Rec_727981,Human_Splice_Rec_727995,Human_Splice_Rec_728009,Human_Splice_Rec_728021,Human_Splice_Rec_728033,Human_Splice_Rec_728043,Human_Splice_Rec_728053 Human_miRNA_ID_2066955,Human_miRNA_ID_2968088 RMVar_hsa_circ_59048,RMVar_hsa_circ_236564,RMVar_hsa_circ_371406,RMVar_hsa_circ_18259,RMVar_hsa_circ_367308 63171 RMVar_ID_63171 Human_SNP_ID_263195578 m1A Human chr5 + 178209400 178209400 178209400 GCAGCAGCAGTATGGCTCTGGGGGCCGTGGAAACCGCAACCGAGGGAACCGAGGCAGCGGAGGTG GCAGCAGCAGTATGGCTCTGGGGGCCGTGGAAGCCGCAACCGAGGGAACCGAGGCAGCGGAGGTG A G HNRNPAB Ensembl:ENSG00000197451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:178209295..178209486;chr5:178209351..178209425 26863196 MeRIP-seq:(Medium) rs752893394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1040881,Human_RBP_ID_7422255,Human_RBP_ID_9175045,Human_RBP_ID_15403016,Human_RBP_ID_26826914 Human_Splice_Rec_727982,Human_Splice_Rec_727983,Human_Splice_Rec_727996,Human_Splice_Rec_727997,Human_Splice_Rec_728010,Human_Splice_Rec_728011,Human_Splice_Rec_728022,Human_Splice_Rec_728023,Human_Splice_Rec_728034,Human_Splice_Rec_728035,Human_Splice_Rec_728044,Human_Splice_Rec_728045,Human_Splice_Rec_728054,Human_Splice_Rec_728055 Human_miRNA_ID_2958824 RMVar_hsa_circ_236564,RMVar_hsa_circ_371406,RMVar_hsa_circ_23183,RMVar_hsa_circ_18259 63172 RMVar_ID_63172 Human_SNP_ID_263195852 m1A Human chr5 - 178210145 178210145 178210145 TGGTTCCAGTAGTTGCCGTAGCCCTGATTCCAACTCTGACTCTGACCTGTGGGGGGAGCAGGGCA TGGTTCCAGTAGTTGCCGTAGCCCTGATTCCAGCTCTGACTCTGACCTGTGGGGGGAGCAGGGCA T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178210136..178210290 26863196 MeRIP-seq:(Medium) rs1554103730 Functional Loss SNV dbSNP153 33..33 33 - - - 63173 RMVar_ID_63173 Human_SNP_ID_263195921 m1A Human chr5 + 178210267 178210255 178210267 CTATGGCTATTACGGCTACGGCCCCGGCTACGACTACAGTAAGTAGGAGAGAGGGAGGCCCCATC CTATGGCTATTACGGCTACGG____________CTACAGTAAGTAGGAGAGAGGGAGGCCCCATC GCCCCGGCTACGA G HNRNPAB Ensembl:ENSG00000197451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:178207147..178210750 32194978 MeRIP-seq:(Medium) rs777822643 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_639253,Human_RBP_ID_15403044,Human_RBP_ID_26826917 Human_Splice_Rec_727985,Human_Splice_Rec_727999,Human_Splice_Rec_728057 RMVar_hsa_circ_23183,RMVar_hsa_circ_236566,RMVar_hsa_circ_279140 63174 RMVar_ID_63174 Human_SNP_ID_263199600 m1A Human chr5 - 178221630 178221630 178221630 GAGAATTCACTGTAAGTTCCTCAAAAAGAGCCAGTTTGAATTGGGGACTAAAACATGTCAGGATT GAGAATTCACTGTAAGTTCCTCAAAAAGAGCCGGTTTGAATTGGGGACTAAAACATGTCAGGATT T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178221603..178221763 26863196 MeRIP-seq:(Medium) rs1170957330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2920279,Human_RBP_ID_15403563 RMVar_hsa_circ_121657,RMVar_hsa_circ_316473,RMVar_hsa_circ_355563,RMVar_hsa_circ_373175,RMVar_hsa_circ_310747,RMVar_hsa_circ_236569,RMVar_hsa_circ_269472,RMVar_hsa_circ_20989,RMVar_hsa_circ_236571 63175 RMVar_ID_63175 Human_SNP_ID_263199601 m1A Human chr5 - 178221630 178221630 178221630 GAGAATTCACTGTAAGTTCCTCAAAAAGAGCCAGTTTGAATTGGGGACTAAAACATGTCAGGATT GAGAATTCACTGTAAGTTCCTCAAAAAGAGCCCGTTTGAATTGGGGACTAAAACATGTCAGGATT T G PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178221603..178221763 26863196 MeRIP-seq:(Medium) rs1170957330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2920279,Human_RBP_ID_15403563 RMVar_hsa_circ_121657,RMVar_hsa_circ_316473,RMVar_hsa_circ_355563,RMVar_hsa_circ_373175,RMVar_hsa_circ_310747,RMVar_hsa_circ_236569,RMVar_hsa_circ_269472,RMVar_hsa_circ_20989,RMVar_hsa_circ_236571 63176 RMVar_ID_63176 Human_SNP_ID_263203052 m1A Human chr5 + 178232013 178232013 178232013 AGTGGGAGGCGACCTCACCCACCGTCCCACCGAGGGCCCCCTCACAGGTCAAGTGTGCTGCCTGT AGTGGGAGGCGACCTCACCCACCGTCCCACCGTGGGCCCCCTCACAGGTCAAGTGTGCTGCCTGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:178231968..178232208;chr5:178231962..178232164 26863196 MeRIP-seq:(Medium) rs1198806388 Functional Loss SNV dbSNP153 33..33 33 - - - 63177 RMVar_ID_63177 Human_SNP_ID_263306868 m1A Human chr5 + 178610511 178610511 178610511 GCATTATGCCTTCATCCTCACTCCACAAACAAAGGACCTTTCTATTCTCCCAATCTCCTGATTCT GCATTATGCCTTCATCCTCACTCCACAAACAACGGACCTTTCTATTCTCCCAATCTCCTGATTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178610465..178610538 26863196 MeRIP-seq:(Medium) rs1410875873 Functional Loss SNV dbSNP153 33..33 33 - - - 63178 RMVar_ID_63178 Human_SNP_ID_263310030 m1A Human chr5 + 178623365 178623365 178623365 CTTGTGACTTCCACGATAGCTTTCATGTCCCCAGCTTTCTCTGCTATCCCAATCAGGACAGTGAG CTTGTGACTTCCACGATAGCTTTCATGTCCCCGGCTTTCTCTGCTATCCCAATCAGGACAGTGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:178623315..178623430 26863196 MeRIP-seq:(Medium) rs1308215285 Functional Loss SNV dbSNP153 33..33 33 - - - 63179 RMVar_ID_63179 Human_SNP_ID_263310036 m1A Human chr5 - 178623379 178623379 178623379 GCATTCCAAAAGAACTCACTGTCCTGATTGGGATAGCAGAGAAAGCTGGGGACATGAAAGCTATC GCATTCCAAAAGAACTCACTGTCCTGATTGGGGTAGCAGAGAAAGCTGGGGACATGAAAGCTATC T C CLK4 Ensembl:ENSG00000113240 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178623331..178623444 26863196 MeRIP-seq:(Medium) rs147996509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944886,Human_RBP_ID_4847255 Human_Splice_Rec_728384,Human_Splice_Rec_728408,Human_Splice_Rec_728432,Human_Splice_Rec_728450,Human_Splice_Rec_728484,Human_Splice_Rec_728512,Human_Splice_Rec_728534,Human_Splice_Rec_728556,Human_Splice_Rec_728562,Human_Splice_Rec_728566,Human_Splice_Rec_728570,Human_Splice_Rec_728578 RMVar_hsa_circ_50946 63180 RMVar_ID_63180 Human_SNP_ID_263332783 m1A Human chr5 - 178712441 178712441 178712441 AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCAGCTCTCATTCAACATCAGAGAATGCATACTGG AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCTGCTCTCATTCAACATCAGAGAATGCATACTGG T A AC113348.2,ZNF354A Ensembl:ENSG00000285978,Ensembl:ENSG00000169131 Protein coding,Protein coding intron,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132338 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 63181 RMVar_ID_63181 Human_SNP_ID_263332784 m1A Human chr5 - 178712441 178712441 178712441 AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCAGCTCTCATTCAACATCAGAGAATGCATACTGG AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCCGCTCTCATTCAACATCAGAGAATGCATACTGG T G AC113348.2,ZNF354A Ensembl:ENSG00000285978,Ensembl:ENSG00000169131 Protein coding,Protein coding intron,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132338 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 63182 RMVar_ID_63182 Human_SNP_ID_263337482 m1A Human chr5 - 178729511 178729511 178729511 GAGTCGGGAGATGATTCGTTGGCGGGAGAGAGAGGAACCGGCTGGGAAAGGCTTGAGGCGGAGGG GAGTCGGGAGATGATTCGTTGGCGGGAGAGAGGGGAACCGGCTGGGAAAGGCTTGAGGCGGAGGG T C ZNF354A Ensembl:ENSG00000169131 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178729503..178729598 26863196 MeRIP-seq:(Medium) rs1029214979 Functional Loss SNV dbSNP153 33..33 33 - - - 63183 RMVar_ID_63183 Human_SNP_ID_263337566 m1A Human chr5 - 178729711 178729711 178729711 GAAACCTCGTCTCTACTAAAAATACAAAAATGAGCCGGGCGCCTGTAGTCCCAGCTACTCGGGAG GAAACCTCGTCTCTACTAAAAATACAAAAATGTGCCGGGCGCCTGTAGTCCCAGCTACTCGGGAG T A ZNF354A Ensembl:ENSG00000169131 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178729709..178729853 26863196 MeRIP-seq:(Medium) rs1191773505 Functional Loss SNV dbSNP153 33..33 33 - - - 63184 RMVar_ID_63184 Human_SNP_ID_263367525 m1A Human chr5 - 178829525 178829525 178829525 AGAGAGCAAGCTAAGATGAGAAAAAGCACTGCAGAAAACATTCTGAAGGAGAGAGGAGGGGCAGA AGAGAGCAAGCTAAGATGAGAAAAAGCACTGCGGAAAACATTCTGAAGGAGAGAGGAGGGGCAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178829476..178829574 26863196 MeRIP-seq:(Medium) rs1431582320 Functional Loss SNV dbSNP153 33..33 33 - - - 63185 RMVar_ID_63185 Human_SNP_ID_263368362 m1A Human chr5 - 178831904 178831904 178831904 TGCAATGCCTGTGGCAGGGATGGGTTGTGGACACTATCGGGTGCTACACTGCCAGCGCTGCCAGC TGCAATGCCTGTGGCAGGGATGGGTTGTGGACGCTATCGGGTGCTACACTGCCAGCGCTGCCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178831853..178831970 26863196 MeRIP-seq:(Medium) rs1014824813 Functional Loss SNV dbSNP153 33..33 33 - - - 63186 RMVar_ID_63186 Human_SNP_ID_263368507 m1A Human chr5 - 178832166 178832166 178832166 CAAGGCAGAGGGCCGGTTGGGTAAGCTATCCCAGGTTACAATCCCAGCAACAATGCCAGCCAACA CAAGGCAGAGGGCCGGTTGGGTAAGCTATCCCTGGTTACAATCCCAGCAACAATGCCAGCCAACA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:178832115..178832234 26863196 MeRIP-seq:(Medium) rs1383677846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2920629 63187 RMVar_ID_63187 Human_SNP_ID_263378876 m1A Human chr5 - 178868194 178868194 178868194 TTCTAATGCCCGTCATGCTGATGGGCTCCCTGACCTCCCTTGAGTCTCGGCCCTGTCACTTACAC TTCTAATGCCCGTCATGCTGATGGGCTCCCTGCCCTCCCTTGAGTCTCGGCCCTGTCACTTACAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:178868171..178868261 26863196 MeRIP-seq:(Medium) rs1201074607 Functional Loss SNV dbSNP153 33..33 33 - - - 63188 RMVar_ID_63188 Human_SNP_ID_263507924 m1A Human chr5 - 179345311 179345311 179345311 TGCAGTCCGGCTGCCATGGATCCGCCGGCGGGAGCCGCTCGCCGCCTGCTCTGCCCCGCGCTGCT TGCAGTCCGGCTGCCATGGATCCGCCGGCGGGGGCCGCTCGCCGCCTGCTCTGCCCCGCGCTGCT T C ADAMTS2 Ensembl:ENSG00000087116 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179345270..179345466 32194978 MeRIP-seq:(Medium) rs1393818759 Functional Loss SNV dbSNP153 33..33 33 - - - 63189 RMVar_ID_63189 Human_SNP_ID_263565857 m1A Human chr5 - 179550616 179550616 179550616 CGGGCCCCGGCCCCGGCTCCAGCTCCGGCTCCAGCTCCCGCCCCCGCCCAGCAGCGCAGCCGCCT CGGGCCCCGGCCCCGGCTCCAGCTCCGGCTCCCGCTCCCGCCCCCGCCCAGCAGCGCAGCCGCCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr5:179550571..179550807;chr5:179550565..179550825 26863196 MeRIP-seq:(Medium) rs1026743910 Functional Loss SNV dbSNP153 33..33 33 - - - 63190 RMVar_ID_63190 Human_SNP_ID_263565860 m1A Human chr5 + 179550619 179550619 179550619 CGGCTGCGCTGCTGGGCGGGGGCGGGAGCTGGAGCCGGAGCTGGAGCCGGGGCCGGGGCCCGGGT CGGCTGCGCTGCTGGGCGGGGGCGGGAGCTGGGGCCGGAGCTGGAGCCGGGGCCGGGGCCCGGGT A G RUFY1 Ensembl:ENSG00000176783 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:179550551..179550725 26863196 MeRIP-seq:(Medium) rs1217083010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78629,Human_RBP_ID_9335513,Human_RBP_ID_9436634,Human_RBP_ID_18425064 63191 RMVar_ID_63191 Human_SNP_ID_263565938 m1A Human chr5 + 179550715 179550715 179550715 CGTGGACCGAAGCCAGCTGCCCGGCCCAGGCGACCTGCGGAGCGCAACGAGGCCGCGGGCGGCCG CGTGGACCGAAGCCAGCTGCCCGGCCCAGGCGGCCTGCGGAGCGCAACGAGGCCGCGGGCGGCCG A G RUFY1 Ensembl:ENSG00000176783 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:179550613..179550728 26863410 MeRIP-seq:(Medium) rs1554112879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9335514,Human_RBP_ID_22459065,Human_RBP_ID_26351868 63192 RMVar_ID_63192 Human_SNP_ID_263565974 m1A Human chr5 + 179550771 179550771 179550771 GGGCGGCCGAGGGCTGGTCGGCGCCCATCCTGACCCTGGCACGCAGGGCCACCGGGAACCTGTCG GGGCGGCCGAGGGCTGGTCGGCGCCCATCCTGGCCCTGGCACGCAGGGCCACCGGGAACCTGTCG A G RUFY1 Ensembl:ENSG00000176783 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:179550646..179550797 26863196 MeRIP-seq:(Medium) rs771646247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9335862 63193 RMVar_ID_63193 Human_SNP_ID_263571186 m1A Human chr5 + 179569019 179569019 179569019 GAGCCAGTGGAGACACAGGAGGGGAGAGTGACAGGAGTCAAGAGGAGACGAGGAGAACTGGGGTC GAGCCAGTGGAGACACAGGAGGGGAGAGTGACGGGAGTCAAGAGGAGACGAGGAGAACTGGGGTC A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:179569013..179569085;chr5:179569014..179569142 26863196 MeRIP-seq:(Medium) rs1309356786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343958,RMVar_hsa_circ_360006,RMVar_hsa_circ_341884,RMVar_hsa_circ_236606,RMVar_hsa_circ_305536,RMVar_hsa_circ_303248,RMVar_hsa_circ_314377,RMVar_hsa_circ_98089,RMVar_hsa_circ_298044,RMVar_hsa_circ_37963,RMVar_hsa_circ_368590,RMVar_hsa_circ_287929,RMVar_hsa_circ_236608,RMVar_hsa_circ_71848,RMVar_hsa_circ_236609,RMVar_hsa_circ_236607 63194 RMVar_ID_63194 Human_SNP_ID_263583299 m1A Human chr5 + 179609388 179609388 179609388 GCCTTCTTCCCGTCCTGTAGCACCACTGCCGGAACTGTGGCCACATCTTCTGCAACACCTGCTCC GCCTTCTTCCCGTCCTGTAGCACCACTGCCGGCACTGTGGCCACATCTTCTGCAACACCTGCTCC A C RUFY1 Ensembl:ENSG00000176783 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179609380..179609483 26863196 MeRIP-seq:(Medium) rs759057875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944902,Human_RBP_ID_9398764,Human_RBP_ID_22681104 Human_Splice_Rec_728990,Human_Splice_Rec_729066,Human_Splice_Rec_729100,Human_Splice_Rec_729162,Human_Splice_Rec_729168 Human_miRNA_ID_2674530,Human_miRNA_ID_2925281 RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_93003,RMVar_hsa_circ_236623 63195 RMVar_ID_63195 Human_SNP_ID_263585520 m1A Human chr5 - 179614645 179614645 179614645 GAATACAATACTCATCTAGGATGTAACAGTGAAGCTGAGTAAACTATAACTGTTAAACTTAAGTT GAATACAATACTCATCTAGGATGTAACAGTGAGGCTGAGTAAACTATAACTGTTAAACTTAAGTT T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs528675391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639456,Human_RBP_ID_1651995,Human_RBP_ID_1993347,Human_RBP_ID_2920824,Human_RBP_ID_7423291,Human_RBP_ID_9175163,Human_RBP_ID_10198558,Human_RBP_ID_15406738,Human_RBP_ID_17303867,Human_RBP_ID_17413183,Human_RBP_ID_17529365,Human_RBP_ID_18045882,Human_RBP_ID_18357214,Human_RBP_ID_18839794,Human_RBP_ID_23051556,Human_RBP_ID_23193173,Human_RBP_ID_24100173,Human_RBP_ID_24505610,Human_RBP_ID_25884875,Human_RBP_ID_26530897,Human_RBP_ID_27079834 RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236624 63196 RMVar_ID_63196 Human_SNP_ID_263585521 m1A Human chr5 - 179614645 179614645 179614645 GAATACAATACTCATCTAGGATGTAACAGTGAAGCTGAGTAAACTATAACTGTTAAACTTAAGTT GAATACAATACTCATCTAGGATGTAACAGTGACGCTGAGTAAACTATAACTGTTAAACTTAAGTT T G HNRNPH1 Ensembl:ENSG00000169045 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs528675391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639456,Human_RBP_ID_1651995,Human_RBP_ID_1993347,Human_RBP_ID_2920824,Human_RBP_ID_7423291,Human_RBP_ID_9175163,Human_RBP_ID_10198558,Human_RBP_ID_15406738,Human_RBP_ID_17303867,Human_RBP_ID_17413183,Human_RBP_ID_17529365,Human_RBP_ID_18045882,Human_RBP_ID_18357214,Human_RBP_ID_18839794,Human_RBP_ID_23051556,Human_RBP_ID_23193173,Human_RBP_ID_24100173,Human_RBP_ID_24505610,Human_RBP_ID_25884875,Human_RBP_ID_26530897,Human_RBP_ID_27079834 RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236624 63197 RMVar_ID_63197 Human_SNP_ID_263585672 m1A Human chr5 + 179614913 179614913 179614913 AACCCTCCCATTCCGTTCACGCCCATAGATGCACGGCTTCCACTACTGTAGTAGCTGCTGTTCAC AACCCTCCCATTCCGTTCACGCCCATAGATGCGCGGCTTCCACTACTGTAGTAGCTGCTGTTCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:179614865..179614976;chr5:179614866..179614955 26863196 MeRIP-seq:(Medium) rs1427114545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236628 63198 RMVar_ID_63198 Human_SNP_ID_263585683 m1A Human chr5 - 179614936 179614933 179614936 TCTTTGCAGGTAACCAAGGAGCAGTGAACAGCAGCTACTACAGTAGTGGAAGCCGTGCATCTATG TCTTTGCAGGTAACCAAGGAGCAGTGAACAGC___TACTACAGTAGTGGAAGCCGTGCATCTATG AGCT A HNRNPH1 Ensembl:ENSG00000169045 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:179614887..179614987 26863196 MeRIP-seq:(Medium) rs1436550575 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_76596,Human_RBP_ID_639461,Human_RBP_ID_946697,Human_RBP_ID_1651997,Human_RBP_ID_1993351,Human_RBP_ID_4826021,Human_RBP_ID_7423304,Human_RBP_ID_15406752,Human_RBP_ID_18448605,Human_RBP_ID_18839800,Human_RBP_ID_22613920,Human_RBP_ID_22681105,Human_RBP_ID_22746048,Human_RBP_ID_22828001,Human_RBP_ID_24100183,Human_RBP_ID_24505622,Human_RBP_ID_25884898 Human_Splice_Rec_729210,Human_Splice_Rec_729222,Human_Splice_Rec_729248,Human_Splice_Rec_729272,Human_Splice_Rec_729302,Human_Splice_Rec_729324,Human_Splice_Rec_729346,Human_Splice_Rec_729368,Human_Splice_Rec_729378,Human_Splice_Rec_729380,Human_Splice_Rec_729392,Human_Splice_Rec_729398,Human_Splice_Rec_729410 Human_miRNA_ID_634191 RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_25661,RMVar_hsa_circ_236624 63199 RMVar_ID_63199 Human_SNP_ID_263585874 m1A Human chr5 - 179615526 179615525 179615527 AAACATTGCATAGGTAAATATTTTCTCAAAAAATATAAATTCCCAATAGCAAATACTGATATGTT AAACATTGCATAGGTAAATATTTTCTCAAAA__TATAAATTCCCAATAGCAAATACTGATATGTT ATT A HNRNPH1 Ensembl:ENSG00000169045 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179615524..179615625 32194978 MeRIP-seq:(Medium) rs755590415 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5396441,Human_RBP_ID_8133990,Human_RBP_ID_15406804,Human_RBP_ID_24509243,Human_RBP_ID_25884919 Human_Splice_Rec_729208,Human_Splice_Rec_729220,Human_Splice_Rec_729246,Human_Splice_Rec_729270,Human_Splice_Rec_729300,Human_Splice_Rec_729344,Human_Splice_Rec_729366,Human_Splice_Rec_729376,Human_Splice_Rec_729390,Human_Splice_Rec_729408,Human_Splice_Rec_729424 RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236624 63200 RMVar_ID_63200 Human_SNP_ID_263585877 m1A Human chr5 - 179615526 179615526 179615526 AAACATTGCATAGGTAAATATTTTCTCAAAAAATATAAATTCCCAATAGCAAATACTGATATGTT AAACATTGCATAGGTAAATATTTTCTCAAAAAGTATAAATTCCCAATAGCAAATACTGATATGTT T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179615524..179615625 32194978 MeRIP-seq:(Medium) rs1350140457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5396441,Human_RBP_ID_8133990,Human_RBP_ID_15406804,Human_RBP_ID_24509243,Human_RBP_ID_25884919 Human_Splice_Rec_729208,Human_Splice_Rec_729220,Human_Splice_Rec_729246,Human_Splice_Rec_729270,Human_Splice_Rec_729300,Human_Splice_Rec_729344,Human_Splice_Rec_729366,Human_Splice_Rec_729376,Human_Splice_Rec_729390,Human_Splice_Rec_729408,Human_Splice_Rec_729424 RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236624 63201 RMVar_ID_63201 Human_SNP_ID_263586415 m1A Human chr5 - 179616957 179616957 179616957 CTAACCTTGTATGCCTTTTCTCTCATTTCAGAACACAGATATGTAGAACTCTTCTTGAATTCTAC CTAACCTTGTATGCCTTTTCTCTCATTTCAGAGCACAGATATGTAGAACTCTTCTTGAATTCTAC T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179616921..179617072 32194978 MeRIP-seq:(Medium) rs144410738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1652040,Human_RBP_ID_1993373,Human_RBP_ID_2920864,Human_RBP_ID_5395903,Human_RBP_ID_7423380,Human_RBP_ID_8612074,Human_RBP_ID_10236458,Human_RBP_ID_15406886,Human_RBP_ID_21216282,Human_RBP_ID_22553178,Human_RBP_ID_22613921,Human_RBP_ID_22681109,Human_RBP_ID_22745988,Human_RBP_ID_22828022,Human_RBP_ID_23051580,Human_RBP_ID_24562036,Human_RBP_ID_25884989 Human_Splice_Rec_729204,Human_Splice_Rec_729205,Human_Splice_Rec_729242,Human_Splice_Rec_729243,Human_Splice_Rec_729266,Human_Splice_Rec_729267,Human_Splice_Rec_729296,Human_Splice_Rec_729297,Human_Splice_Rec_729320,Human_Splice_Rec_729321,Human_Splice_Rec_729340,Human_Splice_Rec_729341,Human_Splice_Rec_729372,Human_Splice_Rec_729373,Human_Splice_Rec_729395,Human_Splice_Rec_729405,Human_Splice_Rec_729425,Human_Splice_Rec_729434,Human_Splice_Rec_729435,Human_Splice_Rec_729466,Human_Splice_Rec_729474 Human_miRNA_ID_1464168 RMVar_hsa_circ_2108,RMVar_hsa_circ_236625,RMVar_hsa_circ_96881,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236629,RMVar_hsa_circ_236624,RMVar_hsa_circ_370071,RMVar_hsa_circ_351795,RMVar_hsa_circ_314842,RMVar_hsa_circ_357529,RMVar_hsa_circ_43443,RMVar_hsa_circ_269394,RMVar_hsa_circ_323425 63202 RMVar_ID_63202 Human_SNP_ID_263586747 m1A Human chr5 - 179617902 179617902 179617902 AGACCTCAATTACTGTTTTTCAGGAATGTCTGATCACAGATACGGGGATGGTGGCTCTACTTTCC AGACCTCAATTACTGTTTTTCAGGAATGTCTGGTCACAGATACGGGGATGGTGGCTCTACTTTCC T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179617851..179618075 32194978 MeRIP-seq:(Medium) rs1460465127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76606,Human_RBP_ID_639488,Human_RBP_ID_946704,Human_RBP_ID_1652059,Human_RBP_ID_1993387,Human_RBP_ID_3766835,Human_RBP_ID_3967685,Human_RBP_ID_7423401,Human_RBP_ID_8267491,Human_RBP_ID_8612088,Human_RBP_ID_8888764,Human_RBP_ID_15406922,Human_RBP_ID_17299814,Human_RBP_ID_18839846,Human_RBP_ID_19015385,Human_RBP_ID_21156329,Human_RBP_ID_22512144,Human_RBP_ID_22613922,Human_RBP_ID_22681303,Human_RBP_ID_22828041,Human_RBP_ID_23050200,Human_RBP_ID_23116265,Human_RBP_ID_24100235,Human_RBP_ID_24434155,Human_RBP_ID_25885036,Human_RBP_ID_27739076 Human_Splice_Rec_729198,Human_Splice_Rec_729214,Human_Splice_Rec_729236,Human_Splice_Rec_729260,Human_Splice_Rec_729276,Human_Splice_Rec_729290,Human_Splice_Rec_729314,Human_Splice_Rec_729334,Human_Splice_Rec_729358,Human_Splice_Rec_729382,Human_Splice_Rec_729402,Human_Splice_Rec_729416,Human_Splice_Rec_729448,Human_Splice_Rec_729460,Human_Splice_Rec_729470,Human_Splice_Rec_729482 Human_miRNA_ID_1346031,Human_miRNA_ID_2568004 RMVar_hsa_circ_2108,RMVar_hsa_circ_236625,RMVar_hsa_circ_126787,RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236629,RMVar_hsa_circ_370071,RMVar_hsa_circ_43443,RMVar_hsa_circ_4207,RMVar_hsa_circ_269394,RMVar_hsa_circ_62711,RMVar_hsa_circ_60419,RMVar_hsa_circ_358056,RMVar_hsa_circ_346884,RMVar_hsa_circ_126859,RMVar_hsa_circ_361522,RMVar_hsa_circ_64184,RMVar_hsa_circ_236632 63203 RMVar_ID_63203 Human_SNP_ID_263587216 m1A Human chr5 + 179619325 179619325 179619325 TTCTTTAGAGCCTTTTCAGCTATTTCCTGTGAAGCAAACTGCACGAAGGCCTCCCCCGTACTCCT TTCTTTAGAGCCTTTTCAGCTATTTCCTGTGAGGCAAACTGCACGAAGGCCTCCCCCGTACTCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179619276..179619425 32194978 MeRIP-seq:(Medium) rs1356693393 Functional Loss SNV dbSNP153 33..33 33 - - - 63204 RMVar_ID_63204 Human_SNP_ID_263588427 m1A Human chr5 - 179622745 179622745 179622745 GACTTTGTTTTCTTTACCTATCTTTGAACACCAGCTTTTCTTTTATGGGTGTCTTTTTTTCTTTT GACTTTGTTTTCTTTACCTATCTTTGAACACCGGCTTTTCTTTTATGGGTGTCTTTTTTTCTTTT T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179622737..179622886 26863196 MeRIP-seq:(Medium) rs1165572195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1652183,Human_RBP_ID_2921040,Human_RBP_ID_3766897,Human_RBP_ID_7423556,Human_RBP_ID_10198810,Human_RBP_ID_15407282,Human_RBP_ID_18839985,Human_RBP_ID_19127653,Human_RBP_ID_23043722,Human_RBP_ID_25885360 RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236629,RMVar_hsa_circ_370071,RMVar_hsa_circ_64184,RMVar_hsa_circ_94037,RMVar_hsa_circ_71058,RMVar_hsa_circ_236638,RMVar_hsa_circ_361114,RMVar_hsa_circ_236640 63205 RMVar_ID_63205 Human_SNP_ID_263588723 m1A Human chr5 - 179623136 179623136 179623136 GCAGTTTGTTTCGACGCCGGACCGCGTAAGAGACGATGATGTTGGGCACGGAAGGTGGAGAGGGA GCAGTTTGTTTCGACGCCGGACCGCGTAAGAGTCGATGATGTTGGGCACGGAAGGTGGAGAGGGA T A HNRNPH1 Ensembl:ENSG00000169045 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:179622767..179623302;chr5:179622882..179623213;chr5:179622951..179623326;chr5:179622951..179623197 26863196 MeRIP-seq:(Medium) rs760348844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76635,Human_RBP_ID_250357,Human_RBP_ID_839734,Human_RBP_ID_946722,Human_RBP_ID_1140748,Human_RBP_ID_1652194,Human_RBP_ID_1993450,Human_RBP_ID_3766899,Human_RBP_ID_4826142,Human_RBP_ID_5212721,Human_RBP_ID_5610732,Human_RBP_ID_7423570,Human_RBP_ID_8612200,Human_RBP_ID_9398781,Human_RBP_ID_10198819,Human_RBP_ID_15407303,Human_RBP_ID_18425065,Human_RBP_ID_18839995,Human_RBP_ID_19016308,Human_RBP_ID_22099893,Human_RBP_ID_22299626,Human_RBP_ID_22512166,Human_RBP_ID_22828161,Human_RBP_ID_23043731,Human_RBP_ID_24100363,Human_RBP_ID_25885368,Human_RBP_ID_26350582 Human_Splice_Rec_729186,Human_Splice_Rec_729187,Human_Splice_Rec_729224,Human_Splice_Rec_729225,Human_Splice_Rec_729249,Human_Splice_Rec_729280,Human_Splice_Rec_729281,Human_Splice_Rec_729303,Human_Splice_Rec_729325,Human_Splice_Rec_729347,Human_Splice_Rec_729438,Human_Splice_Rec_729439,Human_Splice_Rec_729476,Human_Splice_Rec_729477,Human_Splice_Rec_729484,Human_Splice_Rec_729485,Human_Splice_Rec_729502,Human_Splice_Rec_729503,Human_Splice_Rec_729510,Human_Splice_Rec_729511,Human_Splice_Rec_729518,Human_Splice_Rec_729519,Human_Splice_Rec_729526,Human_Splice_Rec_729527,Human_Splice_Rec_729536,Human_Splice_Rec_729537,Human_Splice_Rec_729544,Human_Splice_Rec_729545,Human_Splice_Rec_729560,Human_Splice_Rec_729561,Human_Splice_Rec_729568,Human_Splice_Rec_729569,Human_Splice_Rec_729575,Human_Splice_Rec_729582,Human_Splice_Rec_729583,Human_Splice_Rec_729590,Human_Splice_Rec_729591,Human_Splice_Rec_729596,Human_Splice_Rec_729597,Human_Splice_Rec_729602,Human_Splice_Rec_729603,Human_Splice_Rec_729610,Human_Splice_Rec_729611,Human_Splice_Rec_729616,Human_Splice_Rec_729617,Human_Splice_Rec_729622,Human_Splice_Rec_729623,Human_Splice_Rec_729626,Human_Splice_Rec_729627,Human_Splice_Rec_729634,Human_Splice_Rec_729635,Human_Splice_Rec_729637,Human_Splice_Rec_729640,Human_Splice_Rec_729642,Human_Splice_Rec_729644 RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236629,RMVar_hsa_circ_370071,RMVar_hsa_circ_64184,RMVar_hsa_circ_94037,RMVar_hsa_circ_71058,RMVar_hsa_circ_236638,RMVar_hsa_circ_361114,RMVar_hsa_circ_236641,RMVar_hsa_circ_115441,RMVar_hsa_circ_310735,RMVar_hsa_circ_236642 63206 RMVar_ID_63206 Human_SNP_ID_263588724 m1A Human chr5 - 179623136 179623136 179623136 GCAGTTTGTTTCGACGCCGGACCGCGTAAGAGACGATGATGTTGGGCACGGAAGGTGGAGAGGGA GCAGTTTGTTTCGACGCCGGACCGCGTAAGAGGCGATGATGTTGGGCACGGAAGGTGGAGAGGGA T C HNRNPH1 Ensembl:ENSG00000169045 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:179622767..179623302;chr5:179622882..179623213;chr5:179622951..179623326;chr5:179622951..179623197 26863196 MeRIP-seq:(Medium) rs760348844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76635,Human_RBP_ID_250357,Human_RBP_ID_839734,Human_RBP_ID_946722,Human_RBP_ID_1140748,Human_RBP_ID_1652194,Human_RBP_ID_1993450,Human_RBP_ID_3766899,Human_RBP_ID_4826142,Human_RBP_ID_5212721,Human_RBP_ID_5610732,Human_RBP_ID_7423570,Human_RBP_ID_8612200,Human_RBP_ID_9398781,Human_RBP_ID_10198819,Human_RBP_ID_15407303,Human_RBP_ID_18425065,Human_RBP_ID_18839995,Human_RBP_ID_19016308,Human_RBP_ID_22099893,Human_RBP_ID_22299626,Human_RBP_ID_22512166,Human_RBP_ID_22828161,Human_RBP_ID_23043731,Human_RBP_ID_24100363,Human_RBP_ID_25885368,Human_RBP_ID_26350582 Human_Splice_Rec_729186,Human_Splice_Rec_729187,Human_Splice_Rec_729224,Human_Splice_Rec_729225,Human_Splice_Rec_729249,Human_Splice_Rec_729280,Human_Splice_Rec_729281,Human_Splice_Rec_729303,Human_Splice_Rec_729325,Human_Splice_Rec_729347,Human_Splice_Rec_729438,Human_Splice_Rec_729439,Human_Splice_Rec_729476,Human_Splice_Rec_729477,Human_Splice_Rec_729484,Human_Splice_Rec_729485,Human_Splice_Rec_729502,Human_Splice_Rec_729503,Human_Splice_Rec_729510,Human_Splice_Rec_729511,Human_Splice_Rec_729518,Human_Splice_Rec_729519,Human_Splice_Rec_729526,Human_Splice_Rec_729527,Human_Splice_Rec_729536,Human_Splice_Rec_729537,Human_Splice_Rec_729544,Human_Splice_Rec_729545,Human_Splice_Rec_729560,Human_Splice_Rec_729561,Human_Splice_Rec_729568,Human_Splice_Rec_729569,Human_Splice_Rec_729575,Human_Splice_Rec_729582,Human_Splice_Rec_729583,Human_Splice_Rec_729590,Human_Splice_Rec_729591,Human_Splice_Rec_729596,Human_Splice_Rec_729597,Human_Splice_Rec_729602,Human_Splice_Rec_729603,Human_Splice_Rec_729610,Human_Splice_Rec_729611,Human_Splice_Rec_729616,Human_Splice_Rec_729617,Human_Splice_Rec_729622,Human_Splice_Rec_729623,Human_Splice_Rec_729626,Human_Splice_Rec_729627,Human_Splice_Rec_729634,Human_Splice_Rec_729635,Human_Splice_Rec_729637,Human_Splice_Rec_729640,Human_Splice_Rec_729642,Human_Splice_Rec_729644 RMVar_hsa_circ_77898,RMVar_hsa_circ_236626,RMVar_hsa_circ_236629,RMVar_hsa_circ_370071,RMVar_hsa_circ_64184,RMVar_hsa_circ_94037,RMVar_hsa_circ_71058,RMVar_hsa_circ_236638,RMVar_hsa_circ_361114,RMVar_hsa_circ_236641,RMVar_hsa_circ_115441,RMVar_hsa_circ_310735,RMVar_hsa_circ_236642 63207 RMVar_ID_63207 Human_SNP_ID_263588993 m1A Human chr5 + 179623638 179623638 179623638 AACTGCAAGCGAGGACCCACCGCGACTCACCTAGACACGCGACTTCTGCGTGGCTAAGACGAAAT AACTGCAAGCGAGGACCCACCGCGACTCACCTCGACACGCGACTTCTGCGTGGCTAAGACGAAAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:179623526..179623675;chr5:179623466..179623700;chr5:179623521..179623700;chr5:179623532..179623700 26863196 MeRIP-seq:(Medium) rs1024856801 Functional Loss SNV dbSNP153 33..33 33 - - - 63208 RMVar_ID_63208 Human_SNP_ID_263605149 m1A Human chr5 + 179679095 179679095 179679095 GTGATCGGCCCAAAACTGCTGCAGCGTCTGCCACAGGCGGCTGGCATGGCTCGTAGCCGAGCACT GTGATCGGCCCAAAACTGCTGCAGCGTCTGCCCCAGGCGGCTGGCATGGCTCGTAGCCGAGCACT A C CANX,HMGB3P22 Ensembl:ENSG00000127022,Ensembl:ENSG00000225051 Protein coding,Pseudogene intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179679081..179679231 26863196 MeRIP-seq:(Medium) rs116305151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5611695 63209 RMVar_ID_63209 Human_SNP_ID_263610870 m1A Human chr5 + 179699047 179699047 179699047 CCTCCGCCTCTCTCTTTACTGCGGCGCGGGGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCACCC CCTCCGCCTCTCTCTTTACTGCGGCGCGGGGCCAGGTGTGCGGGCGGGAAGGGGCACGGGCACCC A C CANX Ensembl:ENSG00000127022 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:179698944..179699150 26863410 MeRIP-seq:(Medium) rs897750866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74998,Human_RBP_ID_250047,Human_RBP_ID_639562,Human_RBP_ID_839478,Human_RBP_ID_4826163,Human_RBP_ID_5326681,Human_RBP_ID_5509405,Human_RBP_ID_7423635,Human_RBP_ID_9262401,Human_RBP_ID_9335518,Human_RBP_ID_17415468,Human_RBP_ID_22403081,Human_RBP_ID_22459431,Human_RBP_ID_27335427 Human_Splice_Rec_729759,Human_Splice_Rec_729797,Human_Splice_Rec_729803,Human_Splice_Rec_729831,Human_Splice_Rec_729837,Human_Splice_Rec_729847,Human_Splice_Rec_729861,Human_Splice_Rec_729869,Human_Splice_Rec_729895 Human_miRNA_ID_2402081 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 63210 RMVar_ID_63210 Human_SNP_ID_263610873 m1A Human chr5 + 179699063 179699063 179699063 TACTGCGGCGCGGGGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCACCCCCGCGGTCCCCGGGAG TACTGCGGCGCGGGGCAAGGTGTGCGGGCGGGGAGGGGCACGGGCACCCCCGCGGTCCCCGGGAG A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:179698961..179699148 26863410 MeRIP-seq:(Medium) rs1486236583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74998,Human_RBP_ID_250047,Human_RBP_ID_639563,Human_RBP_ID_839478,Human_RBP_ID_946099,Human_RBP_ID_4826163,Human_RBP_ID_5326681,Human_RBP_ID_5449713,Human_RBP_ID_7423635,Human_RBP_ID_9262401,Human_RBP_ID_9335518,Human_RBP_ID_17415469,Human_RBP_ID_22459431,Human_RBP_ID_27079986 Human_Splice_Rec_729797,Human_Splice_Rec_729803,Human_Splice_Rec_729831,Human_Splice_Rec_729837,Human_Splice_Rec_729861,Human_Splice_Rec_729869,Human_Splice_Rec_729895 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 63211 RMVar_ID_63211 Human_SNP_ID_263610874 m1A Human chr5 + 179699063 179699063 179699063 TACTGCGGCGCGGGGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCACCCCCGCGGTCCCCGGGAG TACTGCGGCGCGGGGCAAGGTGTGCGGGCGGGTAGGGGCACGGGCACCCCCGCGGTCCCCGGGAG A T CANX Ensembl:ENSG00000127022 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:179698961..179699148 26863410 MeRIP-seq:(Medium) rs1486236583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74998,Human_RBP_ID_250047,Human_RBP_ID_639563,Human_RBP_ID_839478,Human_RBP_ID_946099,Human_RBP_ID_4826163,Human_RBP_ID_5326681,Human_RBP_ID_5449713,Human_RBP_ID_7423635,Human_RBP_ID_9262401,Human_RBP_ID_9335518,Human_RBP_ID_17415469,Human_RBP_ID_22459431,Human_RBP_ID_27079986 Human_Splice_Rec_729797,Human_Splice_Rec_729803,Human_Splice_Rec_729831,Human_Splice_Rec_729837,Human_Splice_Rec_729861,Human_Splice_Rec_729869,Human_Splice_Rec_729895 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 63212 RMVar_ID_63212 Human_SNP_ID_263610879 m1A Human chr5 + 179699070 179699070 179699070 GCGCGGGGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCACCCCCGCGGTCCCCGGGAGGCTAGAG GCGCGGGGCAAGGTGTGCGGGCGGGAAGGGGCGCGGGCACCCCCGCGGTCCCCGGGAGGCTAGAG A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T cell line,total RNA;HEK293T,H2O2 treatment chr5:179698951..179699606;chr5:179698983..179699606 26863196,26863410 MeRIP-seq:(Medium) rs756252202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74998,Human_RBP_ID_250047,Human_RBP_ID_639563,Human_RBP_ID_787797,Human_RBP_ID_839478,Human_RBP_ID_946099,Human_RBP_ID_4826163,Human_RBP_ID_5326681,Human_RBP_ID_5449713,Human_RBP_ID_7423635,Human_RBP_ID_9262401,Human_RBP_ID_9335518,Human_RBP_ID_17415469,Human_RBP_ID_22459431,Human_RBP_ID_27079986 Human_Splice_Rec_729797,Human_Splice_Rec_729803,Human_Splice_Rec_729831,Human_Splice_Rec_729837,Human_Splice_Rec_729861,Human_Splice_Rec_729869,Human_Splice_Rec_729895 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 63213 RMVar_ID_63213 Human_SNP_ID_263610882 m1A Human chr5 + 179699076 179699076 179699076 GGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCACCCCCGCGGTCCCCGGGAGGCTAGAGGTGAGA GGCAAGGTGTGCGGGCGGGAAGGGGCACGGGCCCCCCCGCGGTCCCCGGGAGGCTAGAGGTGAGA A C CANX Ensembl:ENSG00000127022 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:179698951..179699606 26863410 MeRIP-seq:(Medium) rs1293004299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250047,Human_RBP_ID_639563,Human_RBP_ID_787797,Human_RBP_ID_839478,Human_RBP_ID_946099,Human_RBP_ID_1321015,Human_RBP_ID_4826163,Human_RBP_ID_5326681,Human_RBP_ID_7423635,Human_RBP_ID_9262401,Human_RBP_ID_9335518,Human_RBP_ID_17415469,Human_RBP_ID_22459431,Human_RBP_ID_27079986 Human_Splice_Rec_729797,Human_Splice_Rec_729803,Human_Splice_Rec_729831,Human_Splice_Rec_729837,Human_Splice_Rec_729861,Human_Splice_Rec_729869,Human_Splice_Rec_729895 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 63214 RMVar_ID_63214 Human_SNP_ID_263612801 m1A Human chr5 - 179705627 179705627 179705627 TCAGTTAAATGTATTGCCACCTATCAAACTTCATGAAGATCACTAACCACTCTCTCATTTAAAAT TCAGTTAAATGTATTGCCACCTATCAAACTTCGTGAAGATCACTAACCACTCTCTCATTTAAAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179705625..179705802 26863196 MeRIP-seq:(Medium) rs1164961612 Functional Loss SNV dbSNP153 33..33 33 - - - 63215 RMVar_ID_63215 Human_SNP_ID_263612809 m1A Human chr5 - 179705647 179705647 179705647 TCTACACATAAAGAGCAAAATCAGTTAAATGTATTGCCACCTATCAAACTTCATGAAGATCACTA TCTACACATAAAGAGCAAAATCAGTTAAATGTGTTGCCACCTATCAAACTTCATGAAGATCACTA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:179705641..179705779 26863410 MeRIP-seq:(Medium) rs756587021 Functional Loss SNV dbSNP153 33..33 33 - - - 63216 RMVar_ID_63216 Human_SNP_ID_263612856 m1A Human chr5 + 179705730 179705730 179705730 TGCTGTGTATGTTACTGGTGCTTGGAACTGCTATTGTTGAGGCTCATGATGGACATGATGATGAT TGCTGTGTATGTTACTGGTGCTTGGAACTGCTGTTGTTGAGGCTCATGATGGACATGATGATGAT A G CANX Ensembl:ENSG00000127022 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:179705571..179705750 26863196 MeRIP-seq:(Medium) rs756604999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75001,Human_RBP_ID_639564,Human_RBP_ID_1040945,Human_RBP_ID_1212221,Human_RBP_ID_1652212,Human_RBP_ID_1993458,Human_RBP_ID_2921097,Human_RBP_ID_3766923,Human_RBP_ID_4826176,Human_RBP_ID_5326991,Human_RBP_ID_5427195,Human_RBP_ID_7423686,Human_RBP_ID_8612227,Human_RBP_ID_8888784,Human_RBP_ID_9175253,Human_RBP_ID_9306865,Human_RBP_ID_9398783,Human_RBP_ID_15407806,Human_RBP_ID_17707810,Human_RBP_ID_18057718,Human_RBP_ID_18840016,Human_RBP_ID_22403083,Human_RBP_ID_22828168,Human_RBP_ID_23043742,Human_RBP_ID_23136882,Human_RBP_ID_23214400,Human_RBP_ID_24100433,Human_RBP_ID_24505800,Human_RBP_ID_27739128 Human_Splice_Rec_729716,Human_Splice_Rec_729724,Human_Splice_Rec_729732,Human_Splice_Rec_729760,Human_Splice_Rec_729788,Human_Splice_Rec_729800,Human_Splice_Rec_729804,Human_Splice_Rec_729832,Human_Splice_Rec_729840,Human_Splice_Rec_729848,Human_Splice_Rec_729849,Human_Splice_Rec_729870,Human_Splice_Rec_729908 Human_miRNA_ID_2208620,Human_miRNA_ID_2208621,Human_miRNA_ID_3033227,Human_miRNA_ID_3033228 RMVar_hsa_circ_70318,RMVar_hsa_circ_280607,RMVar_hsa_circ_314002,RMVar_hsa_circ_236643,RMVar_hsa_circ_113904,RMVar_hsa_circ_358735,RMVar_hsa_circ_353701,RMVar_hsa_circ_328988,RMVar_hsa_circ_292291,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_275489,RMVar_hsa_circ_277193,RMVar_hsa_circ_269914,RMVar_hsa_circ_236646,RMVar_hsa_circ_236648,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_236647,RMVar_hsa_circ_236644,RMVar_hsa_circ_236645 63217 RMVar_ID_63217 Human_SNP_ID_263616820 m1A Human chr5 + 179719754 179719754 179719754 CTGGTTAGATGATGAGCCTGAGTACGTACCTGATCCAGACGCAGAGAAACCTGAGGATTGGTAAG CTGGTTAGATGATGAGCCTGAGTACGTACCTGTTCCAGACGCAGAGAAACCTGAGGATTGGTAAG A T CANX Ensembl:ENSG00000127022 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179719631..179719826 26863196 MeRIP-seq:(Medium) rs1313354040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639588,Human_RBP_ID_946107,Human_RBP_ID_1652242,Human_RBP_ID_1993482,Human_RBP_ID_3766946,Human_RBP_ID_5212728,Human_RBP_ID_7423743,Human_RBP_ID_8888799,Human_RBP_ID_9398792,Human_RBP_ID_15408081,Human_RBP_ID_17196752,Human_RBP_ID_17707826,Human_RBP_ID_18840049,Human_RBP_ID_22459933,Human_RBP_ID_22771578,Human_RBP_ID_23136884,Human_RBP_ID_24100472,Human_RBP_ID_26351885,Human_RBP_ID_27514734 Human_Splice_Rec_729746,Human_Splice_Rec_729747,Human_Splice_Rec_729774,Human_Splice_Rec_729775,Human_Splice_Rec_729818,Human_Splice_Rec_729819,Human_Splice_Rec_729858,Human_Splice_Rec_729859,Human_Splice_Rec_729882,Human_Splice_Rec_729883 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_373278,RMVar_hsa_circ_97640,RMVar_hsa_circ_236653,RMVar_hsa_circ_359776,RMVar_hsa_circ_365352,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_49024,RMVar_hsa_circ_236660,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663,RMVar_hsa_circ_271187,RMVar_hsa_circ_236667,RMVar_hsa_circ_35863,RMVar_hsa_circ_345021,RMVar_hsa_circ_272973,RMVar_hsa_circ_358930,RMVar_hsa_circ_236668 63218 RMVar_ID_63218 Human_SNP_ID_263616981 m1A Human chr5 - 179720359 179720359 179720359 AAACAACAAATTATAAACAGGTTCTGTGATGCAGGACTATGAACAGCTGGCTGGCCCAGGGCTGC AAACAACAAATTATAAACAGGTTCTGTGATGCTGGACTATGAACAGCTGGCTGGCCCAGGGCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179720357..179720495 26863196 MeRIP-seq:(Medium) rs375463138 Functional Loss SNV dbSNP153 33..33 33 - - - 63219 RMVar_ID_63219 Human_SNP_ID_263617006 m1A Human chr5 + 179720412 179720412 179720412 AATTTGTTGTTTGTACCTCCGTAGGGATGAAGACATGGATGGAGAATGGGAGGCTCCTCAGATTG AATTTGTTGTTTGTACCTCCGTAGGGATGAAGCCATGGATGGAGAATGGGAGGCTCCTCAGATTG A C CANX Ensembl:ENSG00000127022 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs761684718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946108,Human_RBP_ID_1652246,Human_RBP_ID_1993484,Human_RBP_ID_2921166,Human_RBP_ID_4826219,Human_RBP_ID_8612261,Human_RBP_ID_8888800,Human_RBP_ID_9398795,Human_RBP_ID_17299825,Human_RBP_ID_17707828,Human_RBP_ID_18840050,Human_RBP_ID_22403097,Human_RBP_ID_22459069,Human_RBP_ID_22771581,Human_RBP_ID_24100474,Human_RBP_ID_25885763,Human_RBP_ID_26352983,Human_RBP_ID_27080012,Human_RBP_ID_27335450 Human_Splice_Rec_729748,Human_Splice_Rec_729776,Human_Splice_Rec_729820,Human_Splice_Rec_729860,Human_Splice_Rec_729884 Human_miRNA_ID_847798,Human_miRNA_ID_1386511,Human_miRNA_ID_2213952 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_373278,RMVar_hsa_circ_97640,RMVar_hsa_circ_236653,RMVar_hsa_circ_359776,RMVar_hsa_circ_365352,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_49024,RMVar_hsa_circ_236660,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_270449,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236667,RMVar_hsa_circ_35863,RMVar_hsa_circ_345021,RMVar_hsa_circ_272973,RMVar_hsa_circ_358930 63220 RMVar_ID_63220 Human_SNP_ID_263617671 m1A Human chr5 - 179723001 179723001 179723001 CAGCAAACACGAACCTCAGCAGCCCCATCAGCAGCTTTCTTCAGGCCCCATCCATCATTGGCCCA CAGCAAACACGAACCTCAGCAGCCCCATCAGCGGCTTTCTTCAGGCCCCATCCATCATTGGCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179722904..179723063 26863196 MeRIP-seq:(Medium) rs1474198675 Functional Loss SNV dbSNP153 33..33 33 - - - 63221 RMVar_ID_63221 Human_SNP_ID_263618169 m1A Human chr5 - 179724782 179724782 179724782 TAAAGCAGATTTTCTGGACTCTGTTTCTTACCAAGTTTCTCTTCTCCTTCCTCCTCCTCATCTCC TAAAGCAGATTTTCTGGACTCTGTTTCTTACCGAGTTTCTCTTCTCCTTCCTCCTCCTCATCTCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr5:179724701..179724854;chr5:179724703..179726700 26863410 MeRIP-seq:(Medium) rs763115954 Functional Loss SNV dbSNP153 33..33 33 - - - 63222 RMVar_ID_63222 Human_SNP_ID_263618170 m1A Human chr5 - 179724782 179724782 179724782 TAAAGCAGATTTTCTGGACTCTGTTTCTTACCAAGTTTCTCTTCTCCTTCCTCCTCCTCATCTCC TAAAGCAGATTTTCTGGACTCTGTTTCTTACCCAGTTTCTCTTCTCCTTCCTCCTCCTCATCTCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr5:179724701..179724854;chr5:179724703..179726700 26863410 MeRIP-seq:(Medium) rs763115954 Functional Loss SNV dbSNP153 33..33 33 - - - 63223 RMVar_ID_63223 Human_SNP_ID_263618794 m1A Human chr5 + 179726731 179726729 179726732 TGCTGAAGAAGATGGTGGCACTGTCAGTCAAGAGGAGGAAGACAGAAAACCTAAAGCAGAGGTAA TGCTGAAGAAGATGGTGGCACTGTCAGTCAA___GAGGAAGACAGAAAACCTAAAGCAGAGGTAA AGAG A CANX Ensembl:ENSG00000127022 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:179724742..179726750 26863196 MeRIP-seq:(Medium) rs766342480 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_75019,Human_RBP_ID_214535,Human_RBP_ID_250056,Human_RBP_ID_787810,Human_RBP_ID_839486,Human_RBP_ID_944909,Human_RBP_ID_1993497,Human_RBP_ID_3766962,Human_RBP_ID_4826246,Human_RBP_ID_7423811,Human_RBP_ID_9262417,Human_RBP_ID_9398808,Human_RBP_ID_15408225,Human_RBP_ID_17671756,Human_RBP_ID_17707838,Human_RBP_ID_18045945,Human_RBP_ID_21215748,Human_RBP_ID_22100753,Human_RBP_ID_22403105,Human_RBP_ID_22772229,Human_RBP_ID_23050208,Human_RBP_ID_24548162,Human_RBP_ID_26351897,Human_RBP_ID_27826176 Human_Splice_Rec_729756,Human_Splice_Rec_729757,Human_Splice_Rec_729784,Human_Splice_Rec_729785,Human_Splice_Rec_729828,Human_Splice_Rec_729829,Human_Splice_Rec_729892,Human_Splice_Rec_729893,Human_Splice_Rec_729932,Human_Splice_Rec_729933 RMVar_hsa_circ_309008,RMVar_hsa_circ_97640,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_236660 63224 RMVar_ID_63224 Human_SNP_ID_263618798 m1A Human chr5 + 179726734 179726734 179726734 TGAAGAAGATGGTGGCACTGTCAGTCAAGAGGAGGAAGACAGAAAACCTAAAGCAGAGGTAAAGG TGAAGAAGATGGTGGCACTGTCAGTCAAGAGGCGGAAGACAGAAAACCTAAAGCAGAGGTAAAGG A C CANX Ensembl:ENSG00000127022 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179726632..179726800 26863196 MeRIP-seq:(Medium) rs1474263495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75019,Human_RBP_ID_214535,Human_RBP_ID_787810,Human_RBP_ID_839486,Human_RBP_ID_944909,Human_RBP_ID_1993497,Human_RBP_ID_3766962,Human_RBP_ID_4826246,Human_RBP_ID_7423811,Human_RBP_ID_9398808,Human_RBP_ID_15408225,Human_RBP_ID_17671756,Human_RBP_ID_17707838,Human_RBP_ID_18045945,Human_RBP_ID_21215748,Human_RBP_ID_22100753,Human_RBP_ID_22403105,Human_RBP_ID_22772229,Human_RBP_ID_23050208,Human_RBP_ID_24548162,Human_RBP_ID_26351897,Human_RBP_ID_27826176 Human_Splice_Rec_729756,Human_Splice_Rec_729757,Human_Splice_Rec_729784,Human_Splice_Rec_729785,Human_Splice_Rec_729828,Human_Splice_Rec_729829,Human_Splice_Rec_729892,Human_Splice_Rec_729893,Human_Splice_Rec_729932,Human_Splice_Rec_729933 RMVar_hsa_circ_309008,RMVar_hsa_circ_97640,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_236660 63225 RMVar_ID_63225 Human_SNP_ID_263618805 m1A Human chr5 - 179726761 179726761 179726761 TGGTAAAACAAAATGTGTGACCCCTTTCCTTTACCTCTGCTTTAGGTTTTCTGTCTTCCTCCTCT TGGTAAAACAAAATGTGTGACCCCTTTCCTTTTCCTCTGCTTTAGGTTTTCTGTCTTCCTCCTCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:179726676..179726775 26863196 MeRIP-seq:(Medium) rs111362041 Functional Loss SNV dbSNP153 33..33 33 - - - 63226 RMVar_ID_63226 Human_SNP_ID_263619520 m1A Human chr5 - 179730077 179730077 179730077 TCAGTGTAGAGTAATAATAACATTATTACACTATAGTGGTGTGGGAGAGGCTCTGATAGCACCCA TCAGTGTAGAGTAATAATAACATTATTACACTGTAGTGGTGTGGGAGAGGCTCTGATAGCACCCA T C lnc-CBY3-3 RNACentral:URS0000D56E37 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179730026..179730100 32194978 MeRIP-seq:(Medium) rs1404830208 Functional Loss SNV dbSNP153 33..33 33 - - - 63227 RMVar_ID_63227 Human_SNP_ID_263620283 m1A Human chr5 + 179732876 179732876 179732876 AGATGGCGGCCGCGGCGGTAGCGCGGAAAACAATGGGGCCGGGGCGGTGGGGAGAGGCCGAGGCT AGATGGCGGCCGCGGCGGTAGCGCGGAAAACAGTGGGGCCGGGGCGGTGGGGAGAGGCCGAGGCT A G MAML1 Ensembl:ENSG00000161021 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:179732826..179765489;chr5:179732826..179765347 26863196 MeRIP-seq:(Medium) rs1474136188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839592,Human_RBP_ID_4826358,Human_RBP_ID_5427196,Human_RBP_ID_9335519 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63228 RMVar_ID_63228 Human_SNP_ID_263620284 m1A Human chr5 - 179732877 179732877 179732877 AAGCCTCGGCCTCTCCCCACCGCCCCGGCCCCATTGTTTTCCGCGCTACCGCCGCGGCCGCCATC AAGCCTCGGCCTCTCCCCACCGCCCCGGCCCCGTTGTTTTCCGCGCTACCGCCGCGGCCGCCATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr5:179732826..179733425;chr5:179732826..179733024 26863196 MeRIP-seq:(Medium) rs748899296 Functional Loss SNV dbSNP153 33..33 33 - - - 63229 RMVar_ID_63229 Human_SNP_ID_263620304 m1A Human chr5 - 179732932 179732932 179732932 GTTTTCCTCCTGCCCCGCTCGGCCCGACCCCCAGCCGGCGCTTGCTGCCTACCTCAAGCCTCGGC GTTTTCCTCCTGCCCCGCTCGGCCCGACCCCCTGCCGGCGCTTGCTGCCTACCTCAAGCCTCGGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:179732826..179733088 26863196 MeRIP-seq:(Medium) rs1200151277 Functional Loss SNV dbSNP153 33..33 33 - - - 63230 RMVar_ID_63230 Human_SNP_ID_263620333 m1A Human chr5 + 179733005 179733005 179733005 GCGCGCGAGCCCGCTCCGCTGCCCTCGGGGGCATGGCGCGGCCGTGAGGCGGAGAGGGGTAGCCG GCGCGCGAGCCCGCTCCGCTGCCCTCGGGGGCGTGGCGCGGCCGTGAGGCGGAGAGGGGTAGCCG A G MAML1 Ensembl:ENSG00000161021 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:179732926..179733125 26863196 MeRIP-seq:(Medium) rs534973733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4826373 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63231 RMVar_ID_63231 Human_SNP_ID_263620334 m1A Human chr5 + 179733005 179733005 179733005 GCGCGCGAGCCCGCTCCGCTGCCCTCGGGGGCATGGCGCGGCCGTGAGGCGGAGAGGGGTAGCCG GCGCGCGAGCCCGCTCCGCTGCCCTCGGGGGCTTGGCGCGGCCGTGAGGCGGAGAGGGGTAGCCG A T MAML1 Ensembl:ENSG00000161021 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:179732926..179733125 26863196 MeRIP-seq:(Medium) rs534973733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4826373 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63232 RMVar_ID_63232 Human_SNP_ID_263620505 m1A Human chr5 + 179733399 179733399 179733399 CGCCGCCCCGGCCCCGCGCCTGGACGCCGCTGACGGCCCCGAGCACGGCCGCCCGGCCACGGTGA CGCCGCCCCGGCCCCGCGCCTGGACGCCGCTGTCGGCCCCGAGCACGGCCGCCCGGCCACGGTGA A T MAML1 Ensembl:ENSG00000161021 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:179733351..179733400 26863196 MeRIP-seq:(Medium) rs1000156048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250286,Human_RBP_ID_944911,Human_RBP_ID_4826391,Human_RBP_ID_9335866,Human_RBP_ID_27514775 Human_Splice_Rec_729937 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63233 RMVar_ID_63233 Human_SNP_ID_263622378 m1A Human chr5 + 179740609 179740609 179740609 ATCTTTAAGTTTTGGAAGATGGTTCTGGTGCTAGGTGGAGGATGCCTGGGGTTGGTGTGGATAGG ATCTTTAAGTTTTGGAAGATGGTTCTGGTGCTGGGTGGAGGATGCCTGGGGTTGGTGTGGATAGG A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179740606..179740750 26863196 MeRIP-seq:(Medium) rs1341717948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7424013 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63234 RMVar_ID_63234 Human_SNP_ID_263628083 m1A Human chr5 + 179760335 179760335 179760335 AAGTACTATGGTGTGGGTGGTAGGTGATGTGGATGATGGAGGAGATAAGCCACCTGAATTAGAAG AAGTACTATGGTGTGGGTGGTAGGTGATGTGGGTGATGGAGGAGATAAGCCACCTGAATTAGAAG A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179760332..179760408 26863196 MeRIP-seq:(Medium) rs529764746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63235 RMVar_ID_63235 Human_SNP_ID_263629343 m1A Human chr5 + 179765300 179765299 179765301 CTGTCATAGCAGAGCAAATTCATATGTATCTTAAGTCATTCTTTTCAATGTTTTTCAGCATCTTC CTGTCATAGCAGAGCAAATTCATATGTATCTT__GTCATTCTTTTCAATGTTTTTCAGCATCTTC TAA T MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179765295..179765389 26863196 MeRIP-seq:(Medium) rs1481499939 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8612373 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 63236 RMVar_ID_63236 Human_SNP_ID_263638568 m1A Human chr5 + 179797743 179797743 179797743 GTAGTATATGCATTCCAGTGTTCGCGCCAGAGACGGCGGGCGCCCAAGTAAAAGCTCTTCTAAAA GTAGTATATGCATTCCAGTGTTCGCGCCAGAGCCGGCGGGCGCCCAAGTAAAAGCTCTTCTAAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179797696..179797947 32194978 MeRIP-seq:(Medium) rs1185841868 Functional Loss SNV dbSNP153 33..33 33 - - - 63237 RMVar_ID_63237 Human_SNP_ID_263639204 m1A Human chr5 + 179799216 179799216 179799216 AGCGTGCAGTGCAGCCCACCTTCAGTTTCTGGATCTTGCCAGCCAGCGAGGAGTGAGTGCCCACG AGCGTGCAGTGCAGCCCACCTTCAGTTTCTGGGTCTTGCCAGCCAGCGAGGAGTGAGTGCCCACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179798984..179799299 26863196 MeRIP-seq:(Medium) rs759982479 Functional Loss SNV dbSNP153 33..33 33 - - - 63238 RMVar_ID_63238 Human_SNP_ID_263639486 m1A Human chr5 - 179799937 179799937 179799937 CAGCTGGGCTTCATTGGTGTGCCCCTCCCCTTACCTGACGGTGCCTTTCAGTCCCACCTGCCTCT CAGCTGGGCTTCATTGGTGTGCCCCTCCCCTTCCCTGACGGTGCCTTTCAGTCCCACCTGCCTCT T G MGAT4B Ensembl:ENSG00000161013 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179799933..179800034 32194978 MeRIP-seq:(Medium) rs778157992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88758,RMVar_hsa_circ_105521,RMVar_hsa_circ_236681,RMVar_hsa_circ_66113,RMVar_hsa_circ_236680,RMVar_hsa_circ_236682,RMVar_hsa_circ_125917,RMVar_hsa_circ_376903 63239 RMVar_ID_63239 Human_SNP_ID_263640429 m1A Human chr5 - 179801891 179801891 179801891 TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAAGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCATGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG T A MGAT4B Ensembl:ENSG00000161013 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs78450232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4826620,Human_RBP_ID_9307306,Human_RBP_ID_9398821,Human_RBP_ID_22099904 Human_Splice_Rec_730060,Human_Splice_Rec_730190,Human_Splice_Rec_730218,Human_Splice_Rec_730226,Human_Splice_Rec_730232,Human_Splice_Rec_730236,Human_Splice_Rec_730244 RMVar_hsa_circ_66113 63240 RMVar_ID_63240 Human_SNP_ID_263640430 m1A Human chr5 - 179801891 179801891 179801891 TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAAGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAGGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG T C MGAT4B Ensembl:ENSG00000161013 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs78450232 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4826620,Human_RBP_ID_9307306,Human_RBP_ID_9398821,Human_RBP_ID_22099904 Human_Splice_Rec_730060,Human_Splice_Rec_730190,Human_Splice_Rec_730218,Human_Splice_Rec_730226,Human_Splice_Rec_730232,Human_Splice_Rec_730236,Human_Splice_Rec_730244 RMVar_hsa_circ_66113 63241 RMVar_ID_63241 Human_SNP_ID_263640431 m1A Human chr5 - 179801891 179801891 179801891 TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAAGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCACGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG T G MGAT4B Ensembl:ENSG00000161013 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs78450232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4826620,Human_RBP_ID_9307306,Human_RBP_ID_9398821,Human_RBP_ID_22099904 Human_Splice_Rec_730060,Human_Splice_Rec_730190,Human_Splice_Rec_730218,Human_Splice_Rec_730226,Human_Splice_Rec_730232,Human_Splice_Rec_730236,Human_Splice_Rec_730244 RMVar_hsa_circ_66113 63242 RMVar_ID_63242 Human_SNP_ID_263641236 m1A Human chr5 - 179804530 179804530 179804530 AAAATGGACCCTGGAGAAGGGTTTGGGGCCCAATTTCCTATCTAGCCCGTGCAGCAGCTCTGCCA AAAATGGACCCTGGAGAAGGGTTTGGGGCCCACTTTCCTATCTAGCCCGTGCAGCAGCTCTGCCA T G MGAT4B Ensembl:ENSG00000161013 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179804527..179804708 26863196 MeRIP-seq:(Medium) rs1162437121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134076,Human_RBP_ID_8136725 63243 RMVar_ID_63243 Human_SNP_ID_263641420 m1A Human chr5 + 179805192 179805191 179805192 CAATCCGCGGGCATGTGGCTGCTGCGGGAGGCACACACTGGCTCAGGACAAAGGGCAAGGGCTCA CAATCCGCGGGCATGTGGCTGCTGCGGGAGGC_CACACTGGCTCAGGACAAAGGGCAAGGGCTCA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179805183..179805387 26863196 MeRIP-seq:(Medium) rs557999939 Functional Loss DEL dbSNP153 33..33 33 - - - 63244 RMVar_ID_63244 Human_SNP_ID_263641421 m1A Human chr5 + 179805192 179805192 179805192 CAATCCGCGGGCATGTGGCTGCTGCGGGAGGCACACACTGGCTCAGGACAAAGGGCAAGGGCTCA CAATCCGCGGGCATGTGGCTGCTGCGGGAGGCGCACACTGGCTCAGGACAAAGGGCAAGGGCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179805183..179805387 26863196 MeRIP-seq:(Medium) rs1332259914 Functional Loss SNV dbSNP153 33..33 33 - - - 63245 RMVar_ID_63245 Human_SNP_ID_263641944 m1A Human chr5 - 179806593 179806593 179806593 TGCAGCCTCGGCCCCGCGGGCGCCCGCCGCGCACCCGAGGAGATGAGGCTCCGCAATGGCACCTT TGCAGCCTCGGCCCCGCGGGCGCCCGCCGCGCTCCCGAGGAGATGAGGCTCCGCAATGGCACCTT T A MGAT4B Ensembl:ENSG00000161013 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:179806554..179806655 26863196 MeRIP-seq:(Medium) rs556009554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250860,Human_RBP_ID_4845558,Human_RBP_ID_17090402,Human_RBP_ID_22534043 63246 RMVar_ID_63246 Human_SNP_ID_263642004 m1A Human chr5 + 179806706 179806706 179806706 GCGGCGGCAGGGGCCCCGGCCCCGGGTCGGGGAGGGGCGGGGGGCCCGGGGCCGGGCGGGGACCG GCGGCGGCAGGGGCCCCGGCCCCGGGTCGGGGGGGGGCGGGGGGCCCGGGGCCGGGCGGGGACCG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:179806606..179806827 26863196 MeRIP-seq:(Medium) rs906425616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5214733,Human_RBP_ID_8213335 63247 RMVar_ID_63247 Human_SNP_ID_263642051 m1A Human chr5 + 179806820 179806820 179806820 TACTCAGGGAAGAGGAACAGGCTCAGAAGGGCAGAGGCAGGTATCAGGCTCACTGCAGATATCAG TACTCAGGGAAGAGGAACAGGCTCAGAAGGGCCGAGGCAGGTATCAGGCTCACTGCAGATATCAG A C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:179806442..179807168;chr5:179806676..179807151 26863196 MeRIP-seq:(Medium) rs962934626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5326994,Human_RBP_ID_15409597 63248 RMVar_ID_63248 Human_SNP_ID_263642052 m1A Human chr5 + 179806820 179806820 179806820 TACTCAGGGAAGAGGAACAGGCTCAGAAGGGCAGAGGCAGGTATCAGGCTCACTGCAGATATCAG TACTCAGGGAAGAGGAACAGGCTCAGAAGGGCTGAGGCAGGTATCAGGCTCACTGCAGATATCAG A T SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:179806442..179807168;chr5:179806676..179807151 26863196 MeRIP-seq:(Medium) rs962934626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5326994,Human_RBP_ID_15409597 63249 RMVar_ID_63249 Human_SNP_ID_263646573 m1A Human chr5 + 179820962 179820962 179820962 GCTCGCTATGGCGTCGCTCACCGTGAAGGCCTACCTTCTGGGCAAGGAGGACGCGGCGCGCGAGA GCTCGCTATGGCGTCGCTCACCGTGAAGGCCTGCCTTCTGGGCAAGGAGGACGCGGCGCGCGAGA A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr5:179820901..179821196;chr5:179820901..179820975;chr5:179820901..179821215 26863196 MeRIP-seq:(Medium) rs1295820640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167541,Human_RBP_ID_4846235,Human_RBP_ID_9262418,Human_RBP_ID_22100378 RMVar_hsa_circ_32329 63250 RMVar_ID_63250 Human_SNP_ID_263646598 m1A Human chr5 - 179821012 179821012 179821012 CTCGGCTTCCGCCTCAGGCTCGGGGCTGCAGCAGAAGCTGAAGCGGCGAATCTCGCGCGCCGCGT CTCGGCTTCCGCCTCAGGCTCGGGGCTGCAGCGGAAGCTGAAGCGGCGAATCTCGCGCGCCGCGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179820961..179821209 26863196 MeRIP-seq:(Medium) rs1172565628 Functional Loss SNV dbSNP153 33..33 33 - - - 63251 RMVar_ID_63251 Human_SNP_ID_263646778 m1A Human chr5 + 179821422 179821422 179821422 GCCGGCCGGGGGCTCGAGCCTGGGGGCGTCAGACGCCCCGCTCCACCCCCCGCGCTGTTGGGGAT GCCGGCCGGGGGCTCGAGCCTGGGGGCGTCAGGCGCCCCGCTCCACCCCCCGCGCTGTTGGGGAT A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179821411..179821814 26863196 MeRIP-seq:(Medium) rs1340066079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1321047,Human_RBP_ID_3783981,Human_RBP_ID_8730261 RMVar_hsa_circ_32329 63252 RMVar_ID_63252 Human_SNP_ID_263646794 m1A Human chr5 + 179821453 179821453 179821453 GACGCCCCGCTCCACCCCCCGCGCTGTTGGGGATTTTGGCAAGGACGCGCCGGGGCGAACGCTCT GACGCCCCGCTCCACCCCCCGCGCTGTTGGGGGTTTTGGCAAGGACGCGCCGGGGCGAACGCTCT A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179821449..179822514 26863196 MeRIP-seq:(Medium) rs1288304703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78463,Human_RBP_ID_1321047,Human_RBP_ID_3783982,Human_RBP_ID_5397041,Human_RBP_ID_18502334,Human_RBP_ID_22100755,Human_RBP_ID_22299817,Human_RBP_ID_26791838 RMVar_hsa_circ_32329 63253 RMVar_ID_63253 Human_SNP_ID_263647731 m1A Human chr5 - 179823958 179823958 179823958 CAGACGCTGCACTTGTAGCGGGTTCCTACCACAGGCCCATTGCAGCCATCGCAGATCACATTGGG CAGACGCTGCACTTGTAGCGGGTTCCTACCACGGGCCCATTGCAGCCATCGCAGATCACATTGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179823908..179824030 26863196 MeRIP-seq:(Medium) rs375411629 Functional Loss SNV dbSNP153 33..33 33 - - - 63254 RMVar_ID_63254 Human_SNP_ID_263647786 m1A Human chr5 + 179824064 179824064 179824064 TGCACCGGGGGCACACCAAGCTCGCATTCCCCAGCCCCTTCGGGCACCTGTCTGAGGTGAGCAGG TGCACCGGGGGCACACCAAGCTCGCATTCCCCGGCCCCTTCGGGCACCTGTCTGAGGTGAGCAGG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179824018..179825200 32194978 MeRIP-seq:(Medium) rs377198490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250270,Human_RBP_ID_5509417,Human_RBP_ID_9306885,Human_RBP_ID_18840199,Human_RBP_ID_19125137,Human_RBP_ID_22460360,Human_RBP_ID_27514896,Human_RBP_ID_27567506 Human_Splice_Rec_730259,Human_Splice_Rec_730273,Human_Splice_Rec_730285,Human_Splice_Rec_730291,Human_Splice_Rec_730309,Human_Splice_Rec_730319,Human_Splice_Rec_730329,Human_Splice_Rec_730335,Human_Splice_Rec_730337 Human_miRNA_ID_2384090,Human_miRNA_ID_2683655,Human_miRNA_ID_2889835 RMVar_hsa_circ_122538,RMVar_hsa_circ_90902,RMVar_hsa_circ_32329,RMVar_hsa_circ_317870,RMVar_hsa_circ_355912,RMVar_hsa_circ_292810,RMVar_hsa_circ_236688,RMVar_hsa_circ_236689,RMVar_hsa_circ_236687,RMVar_hsa_circ_274741,RMVar_hsa_circ_236690 63255 RMVar_ID_63255 Human_SNP_ID_263650770 m1A Human chr5 + 179833098 179833098 179833098 GAAAAGAAGCCGCCTGACCCCCGTCTCTCCAGAGAGTTCCAGCACAGAGGAGAAGAGCAGCTCAC GAAAAGAAGCCGCCTGACCCCCGTCTCTCCAGGGAGTTCCAGCACAGAGGAGAAGAGCAGCTCAC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:179833051..179833254 26863196 MeRIP-seq:(Medium) rs747803543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76234,Human_RBP_ID_639849,Human_RBP_ID_945786,Human_RBP_ID_1652404,Human_RBP_ID_18840205,Human_RBP_ID_22403133,Human_RBP_ID_23116268,Human_RBP_ID_26351901 Human_Splice_Rec_730314,Human_Splice_Rec_730324,Human_Splice_Rec_730334,Human_Splice_Rec_730342 Human_miRNA_ID_136646,Human_miRNA_ID_2792166 RMVar_hsa_circ_90902,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236688,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_101584,RMVar_hsa_circ_355456,RMVar_hsa_circ_236691 63256 RMVar_ID_63256 Human_SNP_ID_263650785 m1A Human chr5 - 179833127 179833127 179833127 GCTGGGGTCAGAGCAGCAGCTGCTTGGCTGTGAGCTGCTCTTCTCCTCTGTGCTGGAACTCTCTG GCTGGGGTCAGAGCAGCAGCTGCTTGGCTGTGGGCTGCTCTTCTCCTCTGTGCTGGAACTCTCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:179833076..179833287 26863196 MeRIP-seq:(Medium) rs764205744 Functional Loss SNV dbSNP153 33..33 33 - - - 63257 RMVar_ID_63257 Human_SNP_ID_263650807 m1A Human chr5 - 179833168 179833168 179833168 GCCAGAGACTGCGTGGCGCCCTCAACATTCCCACCCGGCTTGCTGGGGTCAGAGCAGCAGCTGCT GCCAGAGACTGCGTGGCGCCCTCAACATTCCCTCCCGGCTTGCTGGGGTCAGAGCAGCAGCTGCT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:179833026..179833287 26863196 MeRIP-seq:(Medium) rs780729747 Functional Loss SNV dbSNP153 33..33 33 - - - 63258 RMVar_ID_63258 Human_SNP_ID_263650811 m1A Human chr5 - 179833176 179833176 179833176 TCTGCTCCGCCAGAGACTGCGTGGCGCCCTCAACATTCCCACCCGGCTTGCTGGGGTCAGAGCAG TCTGCTCCGCCAGAGACTGCGTGGCGCCCTCAGCATTCCCACCCGGCTTGCTGGGGTCAGAGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179833051..179833277 26863196 MeRIP-seq:(Medium) rs1181662143 Functional Loss SNV dbSNP153 33..33 33 - - - 63259 RMVar_ID_63259 Human_SNP_ID_263650838 m1A Human chr5 + 179833211 179833211 179833211 AGGGCGCCACGCAGTCTCTGGCGGAGCAGATGAGGAAGATCGCCTTGGAGTCCGAGGGGCGCCCT AGGGCGCCACGCAGTCTCTGGCGGAGCAGATGGGGAAGATCGCCTTGGAGTCCGAGGGGCGCCCT A G SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:179833125..179833212 26863410 MeRIP-seq:(Medium) rs545080321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639851,Human_RBP_ID_839352,Human_RBP_ID_943236,Human_RBP_ID_8612457,Human_RBP_ID_8894285,Human_RBP_ID_19015406,Human_RBP_ID_22460364 Human_Splice_Rec_730325 Human_miRNA_ID_2998086 RMVar_hsa_circ_90902,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236688,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_101584,RMVar_hsa_circ_355456,RMVar_hsa_circ_236691 63260 RMVar_ID_63260 Human_SNP_ID_263650839 m1A Human chr5 + 179833211 179833211 179833213 AGGGCGCCACGCAGTCTCTGGCGGAGCAGATGAGGAAGATCGCCTTGGAGTCCGAGGGGCGCCCT AGGGCGCCACGCAGTCTCTGGCGGAGCAGATGGGAAAGATCGCCTTGGAGTCCGAGGGGCGCCCT AGG GGA SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:179833125..179833212 26863410 MeRIP-seq:(Medium) rs1554091355 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_639851,Human_RBP_ID_839352,Human_RBP_ID_943236,Human_RBP_ID_8612457,Human_RBP_ID_8894285,Human_RBP_ID_19015406,Human_RBP_ID_22460364 Human_Splice_Rec_730325 Human_miRNA_ID_2998086 RMVar_hsa_circ_90902,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236688,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_101584,RMVar_hsa_circ_355456,RMVar_hsa_circ_236691 63261 RMVar_ID_63261 Human_SNP_ID_263650842 m1A Human chr5 + 179833214 179833214 179833214 GCGCCACGCAGTCTCTGGCGGAGCAGATGAGGAAGATCGCCTTGGAGTCCGAGGGGCGCCCTGAG GCGCCACGCAGTCTCTGGCGGAGCAGATGAGGGAGATCGCCTTGGAGTCCGAGGGGCGCCCTGAG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179833012..179833286 26863196 MeRIP-seq:(Medium) rs1195166145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639851,Human_RBP_ID_839352,Human_RBP_ID_943236,Human_RBP_ID_8612457,Human_RBP_ID_8894285,Human_RBP_ID_19015406,Human_RBP_ID_22460364 Human_Splice_Rec_730325 Human_miRNA_ID_2998086 RMVar_hsa_circ_90902,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236688,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_101584,RMVar_hsa_circ_355456,RMVar_hsa_circ_236691 63262 RMVar_ID_63262 Human_SNP_ID_263650975 m1A Human chr5 - 179833546 179833546 179833546 AAACTCACCATGAGCACACAGGAGACACGCGCAACAGGCCAAGCCTGACCATGGCCCTGGCTCCT AAACTCACCATGAGCACACAGGAGACACGCGCCACAGGCCAAGCCTGACCATGGCCCTGGCTCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179833544..179833826 26863196 MeRIP-seq:(Medium) rs1434560807 Functional Loss SNV dbSNP153 33..33 33 - - - 63263 RMVar_ID_63263 Human_SNP_ID_263651031 m1A Human chr5 + 179833649 179833647 179833650 GGAGATGATGACTGGACCCATCTGTCTTCAAAAGAAGTGGACCCGTCTACAGGTGAACTCCAGTC GGAGATGATGACTGGACCCATCTGTCTTCAA___AAGTGGACCCGTCTACAGGTGAACTCCAGTC AAAG A SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179833576..179833650 32194978 MeRIP-seq:(Medium) rs747073722 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1212269,Human_RBP_ID_1652407,Human_RBP_ID_1993603,Human_RBP_ID_8612460,Human_RBP_ID_18057021,Human_RBP_ID_18840207,Human_RBP_ID_22100382,Human_RBP_ID_22459942,Human_RBP_ID_22512187,Human_RBP_ID_22771862,Human_RBP_ID_23050213,Human_RBP_ID_26352995,Human_RBP_ID_27160479,Human_RBP_ID_27514905 Human_miRNA_ID_2709677 RMVar_hsa_circ_84219,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_355456,RMVar_hsa_circ_372825,RMVar_hsa_circ_236692,RMVar_hsa_circ_236693 63264 RMVar_ID_63264 Human_SNP_ID_263651034 m1A Human chr5 + 179833649 179833649 179833649 GGAGATGATGACTGGACCCATCTGTCTTCAAAAGAAGTGGACCCGTCTACAGGTGAACTCCAGTC GGAGATGATGACTGGACCCATCTGTCTTCAAAGGAAGTGGACCCGTCTACAGGTGAACTCCAGTC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179833576..179833650 32194978 MeRIP-seq:(Medium) rs982817243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1212269,Human_RBP_ID_1652407,Human_RBP_ID_1993603,Human_RBP_ID_8612460,Human_RBP_ID_18057021,Human_RBP_ID_18840207,Human_RBP_ID_22100382,Human_RBP_ID_22459942,Human_RBP_ID_22512187,Human_RBP_ID_22771862,Human_RBP_ID_23050213,Human_RBP_ID_26352995,Human_RBP_ID_27160479,Human_RBP_ID_27514905 Human_miRNA_ID_2709677 RMVar_hsa_circ_84219,RMVar_hsa_circ_32329,RMVar_hsa_circ_292810,RMVar_hsa_circ_236689,RMVar_hsa_circ_73956,RMVar_hsa_circ_355456,RMVar_hsa_circ_372825,RMVar_hsa_circ_236692,RMVar_hsa_circ_236693 63265 RMVar_ID_63265 Human_SNP_ID_263652514 m1A Human chr5 - 179836455 179836455 179836455 AAGCCCATGGACAGCATCTGGGAGAGGGACTCAATCAGCCGCGGGTCAGCCTCTGCCGAAACAGT AAGCCCATGGACAGCATCTGGGAGAGGGACTCGATCAGCCGCGGGTCAGCCTCTGCCGAAACAGT T C MRNIP Ensembl:ENSG00000161010 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179836431..179837150 32194978 MeRIP-seq:(Medium) rs756095586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532132,Human_RBP_ID_18046065 63266 RMVar_ID_63266 Human_SNP_ID_263652554 m1A Human chr5 - 179836541 179836541 179836541 TTGAATACTGGATGGTGTCCAGAGCCGCTCCGATGTCATAGTTCTTGGTCTGCAGGAGCCTGGTG TTGAATACTGGATGGTGTCCAGAGCCGCTCCGCTGTCATAGTTCTTGGTCTGCAGGAGCCTGGTG T G MRNIP Ensembl:ENSG00000161010 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:179836492..179836830 26863196 MeRIP-seq:(Medium) rs1561609760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532132 63267 RMVar_ID_63267 Human_SNP_ID_263653033 m1A Human chr5 - 179837531 179837529 179837531 GGGCCACACACCCCGTCACATCTGGGTCTGAGAGGCCTTGCGGGAAGACCTCATGGGACGCAAGG GGGCCACACACCCCGTCACATCTGGGTCTGAG__GCCTTGCGGGAAGACCTCATGGGACGCAAGG CCT C MRNIP Ensembl:ENSG00000161010 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179837481..179837631 32194978 MeRIP-seq:(Medium) rs757109530 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_639877,Human_RBP_ID_15410119 63268 RMVar_ID_63268 Human_SNP_ID_263653152 m1A Human chr5 - 179837774 179837774 179837774 GGGAGCTGAGGGGTCCTGGGAAGGAGCTATGGAGTCCCATCCAGCAGGTTACAGCCACATCCTCT GGGAGCTGAGGGGTCCTGGGAAGGAGCTATGGGGTCCCATCCAGCAGGTTACAGCCACATCCTCT T C MRNIP Ensembl:ENSG00000161010 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:179837751..179837775 32194978 MeRIP-seq:(Medium) rs748097828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_639881,Human_RBP_ID_23050329,Human_RBP_ID_25886162 Human_Splice_Rec_730357,Human_Splice_Rec_730371,Human_Splice_Rec_730381,Human_Splice_Rec_730383 63269 RMVar_ID_63269 Human_SNP_ID_263660031 m1A Human chr5 + 179858754 179858754 179858754 CCGCCAGACCTGGTGCGCCTGGAAGAGGCGGCAGCTGCAGCAGCGTAGCACCCGAGAACGCTGAA CCGCCAGACCTGGTGCGCCTGGAAGAGGCGGCGGCTGCAGCAGCGTAGCACCCGAGAACGCTGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179858718..179858817 26863196 MeRIP-seq:(Medium) rs1265918682 Functional Loss SNV dbSNP153 33..33 33 - - - 63270 RMVar_ID_63270 Human_SNP_ID_263662581 m1A Human chr5 - 179866536 179866536 179866536 CCAGAGAGGTGTGCCCTTCACTGCCACCAGACAGCCAGCGAGAGCAGCTCAGAACTGGGGTGCTG CCAGAGAGGTGTGCCCTTCACTGCCACCAGACGGCCAGCGAGAGCAGCTCAGAACTGGGGTGCTG T C TBC1D9B Ensembl:ENSG00000197226 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179866532..179866633 32194978 MeRIP-seq:(Medium) rs901728147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114953,RMVar_hsa_circ_236700 63271 RMVar_ID_63271 Human_SNP_ID_263666004 m1A Human chr5 + 179878355 179878354 179878355 TGGTGGGGTTTCGGAAGGCATAGGCAGTCAGCACCCGCCGGAGGGCAGCAATCCCCAGCTCGTTC TGGTGGGGTTTCGGAAGGCATAGGCAGTCAGC_CCCGCCGGAGGGCAGCAATCCCCAGCTCGTTC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179878265..179878474 26863196 MeRIP-seq:(Medium) rs1561638520 Functional Loss DEL dbSNP153 33..33 33 - - - 63272 RMVar_ID_63272 Human_SNP_ID_263668096 m1A Human chr5 - 179886091 179886091 179886091 CTCTCTGTTGCTCATGGGCAACCTCTCTGATCAGGCAGCACTGGAGGAGAAACTCGAAAGAAGCA CTCTCTGTTGCTCATGGGCAACCTCTCTGATCGGGCAGCACTGGAGGAGAAACTCGAAAGAAGCA T C TBC1D9B Ensembl:ENSG00000197226 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179886089..179886190 26863196 MeRIP-seq:(Medium) rs552760453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15410882 RMVar_hsa_circ_236702,RMVar_hsa_circ_121729,RMVar_hsa_circ_94254,RMVar_hsa_circ_236703,RMVar_hsa_circ_236704 63273 RMVar_ID_63273 Human_SNP_ID_263669541 m1A Human chr5 + 179891452 179891452 179891452 TGCTGGCGAAGCAGATGTAGTTGTTGGAGATGAACATCTGGCCAGGGATGTGCAGCTTGTTGAAC TGCTGGCGAAGCAGATGTAGTTGTTGGAGATGGACATCTGGCCAGGGATGTGCAGCTTGTTGAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179891401..179891562 32194978 MeRIP-seq:(Medium) rs748053918 Functional Loss SNV dbSNP153 33..33 33 - - - 63274 RMVar_ID_63274 Human_SNP_ID_263670102 m1A Human chr5 + 179893433 179893433 179893433 TCGGGGAAGAGCAGGGTGGCGTTCTTCTCCAGACGCGTTATGTCCACCCACTGCACCACGAGGCT TCGGGGAAGAGCAGGGTGGCGTTCTTCTCCAGGCGCGTTATGTCCACCCACTGCACCACGAGGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179893383..179894525 32194978 MeRIP-seq:(Medium) rs759139394 Functional Loss SNV dbSNP153 33..33 33 - - - 63275 RMVar_ID_63275 Human_SNP_ID_263670498 m1A Human chr5 - 179894577 179894577 179894577 CATCGCAGAAGAGAACAAGAACCTGCAGCCCCAGGGAGACGAGGACCCCGGGAAGTTCAAGGAGG CATCGCAGAAGAGAACAAGAACCTGCAGCCCCTGGGAGACGAGGACCCCGGGAAGTTCAAGGAGG T A TBC1D9B Ensembl:ENSG00000197226 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179894451..179894586 26863196 MeRIP-seq:(Medium) rs777610547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250466,Human_RBP_ID_943242,Human_RBP_ID_3968516,Human_RBP_ID_5610752,Human_RBP_ID_9398829,Human_RBP_ID_18195289,Human_RBP_ID_19015423,Human_RBP_ID_22613959,Human_RBP_ID_26351914,Human_RBP_ID_26827744,Human_RBP_ID_27080446,Human_RBP_ID_27826188 Human_Splice_Rec_730562,Human_Splice_Rec_730602,Human_Splice_Rec_730708,Human_Splice_Rec_730714 RMVar_hsa_circ_920,RMVar_hsa_circ_121729,RMVar_hsa_circ_236703,RMVar_hsa_circ_62870,RMVar_hsa_circ_335118,RMVar_hsa_circ_236704,RMVar_hsa_circ_308962,RMVar_hsa_circ_236707,RMVar_hsa_circ_117647,RMVar_hsa_circ_297413,RMVar_hsa_circ_236708,RMVar_hsa_circ_236709,RMVar_hsa_circ_369289,RMVar_hsa_circ_339204,RMVar_hsa_circ_236710 63276 RMVar_ID_63276 Human_SNP_ID_263670499 m1A Human chr5 - 179894577 179894577 179894577 CATCGCAGAAGAGAACAAGAACCTGCAGCCCCAGGGAGACGAGGACCCCGGGAAGTTCAAGGAGG CATCGCAGAAGAGAACAAGAACCTGCAGCCCCGGGGAGACGAGGACCCCGGGAAGTTCAAGGAGG T C TBC1D9B Ensembl:ENSG00000197226 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179894451..179894586 26863196 MeRIP-seq:(Medium) rs777610547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250466,Human_RBP_ID_943242,Human_RBP_ID_3968516,Human_RBP_ID_5610752,Human_RBP_ID_9398829,Human_RBP_ID_18195289,Human_RBP_ID_19015423,Human_RBP_ID_22613959,Human_RBP_ID_26351914,Human_RBP_ID_26827744,Human_RBP_ID_27080446,Human_RBP_ID_27826188 Human_Splice_Rec_730562,Human_Splice_Rec_730602,Human_Splice_Rec_730708,Human_Splice_Rec_730714 RMVar_hsa_circ_920,RMVar_hsa_circ_121729,RMVar_hsa_circ_236703,RMVar_hsa_circ_62870,RMVar_hsa_circ_335118,RMVar_hsa_circ_236704,RMVar_hsa_circ_308962,RMVar_hsa_circ_236707,RMVar_hsa_circ_117647,RMVar_hsa_circ_297413,RMVar_hsa_circ_236708,RMVar_hsa_circ_236709,RMVar_hsa_circ_369289,RMVar_hsa_circ_339204,RMVar_hsa_circ_236710 63277 RMVar_ID_63277 Human_SNP_ID_263673261 m1A Human chr5 - 179904798 179904798 179904798 TCTCTGCCCTGTTCCCAGGTCTTCTCGTGGGCACCCTGGACGTGGTGCTGGACTCCAGTGCCCGC TCTCTGCCCTGTTCCCAGGTCTTCTCGTGGGCCCCCTGGACGTGGTGCTGGACTCCAGTGCCCGC T G TBC1D9B Ensembl:ENSG00000197226 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179904751..179904869 26863196 MeRIP-seq:(Medium) rs973131872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250990,Human_RBP_ID_4845563,Human_RBP_ID_8888950 Human_Splice_Rec_730558,Human_Splice_Rec_730559,Human_Splice_Rec_730598,Human_Splice_Rec_730599,Human_Splice_Rec_730706,Human_Splice_Rec_730707,Human_Splice_Rec_730712,Human_Splice_Rec_730713 Human_miRNA_ID_2299865,Human_miRNA_ID_2303133,Human_miRNA_ID_2306397 RMVar_hsa_circ_920,RMVar_hsa_circ_121729,RMVar_hsa_circ_236703,RMVar_hsa_circ_335118,RMVar_hsa_circ_236704,RMVar_hsa_circ_236707,RMVar_hsa_circ_111990,RMVar_hsa_circ_236711 63278 RMVar_ID_63278 Human_SNP_ID_263689364 m1A Human chr5 - 179966910 179966910 179966910 CCGAAGATCAGCCCTCGGCGACCTCGCCGGCGACAACTCCCTTGGCCTTGAGCCACTTCGAACTT CCGAAGATCAGCCCTCGGCGACCTCGCCGGCGTCAACTCCCTTGGCCTTGAGCCACTTCGAACTT T A RNF130 Ensembl:ENSG00000113269 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:179966866..179966942 26863196 MeRIP-seq:(Medium) rs754832777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17299918,Human_RBP_ID_17532258,Human_RBP_ID_18046152,Human_RBP_ID_26525530 RMVar_hsa_circ_17312,RMVar_hsa_circ_96706,RMVar_hsa_circ_365049,RMVar_hsa_circ_362044,RMVar_hsa_circ_236712,RMVar_hsa_circ_70937,RMVar_hsa_circ_276857,RMVar_hsa_circ_288857,RMVar_hsa_circ_299717,RMVar_hsa_circ_271088,RMVar_hsa_circ_236714,RMVar_hsa_circ_236716,RMVar_hsa_circ_236717,RMVar_hsa_circ_236715,RMVar_hsa_circ_236713 63279 RMVar_ID_63279 Human_SNP_ID_263691055 m1A Human chr5 - 179973119 179973119 179973119 ACAGGAGGGAAGGGTGTTCAGTGCTCAGAGGTAGGGTCAGGAGTAAGAGAGGGATGGGGTGGATG ACAGGAGGGAAGGGTGTTCAGTGCTCAGAGGTTGGGTCAGGAGTAAGAGAGGGATGGGGTGGATG T A RNF130 Ensembl:ENSG00000113269 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:179973116..179973283 26863196 MeRIP-seq:(Medium) rs1310066962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17312,RMVar_hsa_circ_96706,RMVar_hsa_circ_362044,RMVar_hsa_circ_236712,RMVar_hsa_circ_276857,RMVar_hsa_circ_299717,RMVar_hsa_circ_271088,RMVar_hsa_circ_72146,RMVar_hsa_circ_236714,RMVar_hsa_circ_236716,RMVar_hsa_circ_236717,RMVar_hsa_circ_236715 63280 RMVar_ID_63280 Human_SNP_ID_263691075 m1A Human chr5 - 179973183 179973183 179973183 AATTTGAGACTGAAGATCTCTGGGTGAGTTGCACAGAAGCTGGACTAGCGGGGAATTTGGAAAGA AATTTGAGACTGAAGATCTCTGGGTGAGTTGCGCAGAAGCTGGACTAGCGGGGAATTTGGAAAGA T C RNF130 Ensembl:ENSG00000113269 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179973161..179973320 26863196 MeRIP-seq:(Medium) rs1423479796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15411352 RMVar_hsa_circ_17312,RMVar_hsa_circ_96706,RMVar_hsa_circ_362044,RMVar_hsa_circ_236712,RMVar_hsa_circ_276857,RMVar_hsa_circ_299717,RMVar_hsa_circ_271088,RMVar_hsa_circ_72146,RMVar_hsa_circ_236714,RMVar_hsa_circ_236716,RMVar_hsa_circ_236717,RMVar_hsa_circ_236715 63281 RMVar_ID_63281 Human_SNP_ID_333842926 m1A Human chr7 + 105012677 105012677 105012677 TCCAACAGTCATCTCTTCCTCTTCAGGCCGCCAACGCCGACCGCACCACAGTCTCCTCCGCCCAA TCCAACAGTCATCTCTTCCTCTTCAGGCCGCCGACGCCGACCGCACCACAGTCTCCTCCGCCCAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:105012579..105012793;chr7:105012573..105012985 26863196 MeRIP-seq:(Medium) rs1421016598 Functional Loss SNV dbSNP153 33..33 33 - - - 63282 RMVar_ID_63282 Human_SNP_ID_333843226 m1A Human chr7 + 105013407 105013407 105013407 ATATAAAGGAATTCCCACTCCCCTCCCCGCACATTGTCCCACCGGTGGGGAAATCCTTCCCCGAG ATATAAAGGAATTCCCACTCCCCTCCCCGCACCTTGTCCCACCGGTGGGGAAATCCTTCCCCGAG A C lnc-LHFPL3-4 RNACentral:URS00009B30C9 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105013356..105013603 26863196 MeRIP-seq:(Medium) rs1265926686 Functional Loss SNV dbSNP153 33..33 33 - - - 63283 RMVar_ID_63283 Human_SNP_ID_333843645 m1A Human chr7 + 105014251 105014251 105014251 TGACACTGAGCGGGCGCAGGGGGCCGAGTCGGAGACCGTGCCGGAGTTCGGGAGCGGCAACAGAG TGACACTGAGCGGGCGCAGGGGGCCGAGTCGGCGACCGTGCCGGAGTTCGGGAGCGGCAACAGAG A C KMT2E Ensembl:ENSG00000005483 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:105014162..105014528;chr7:105014201..105014579;chr7:105014201..105014526 26863196 MeRIP-seq:(Medium) rs953252278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842969,Human_RBP_ID_5153029,Human_RBP_ID_8653533,Human_RBP_ID_18426549,Human_RBP_ID_23080128,Human_RBP_ID_24181638 63284 RMVar_ID_63284 Human_SNP_ID_333843646 m1A Human chr7 + 105014251 105014251 105014251 TGACACTGAGCGGGCGCAGGGGGCCGAGTCGGAGACCGTGCCGGAGTTCGGGAGCGGCAACAGAG TGACACTGAGCGGGCGCAGGGGGCCGAGTCGGGGACCGTGCCGGAGTTCGGGAGCGGCAACAGAG A G KMT2E Ensembl:ENSG00000005483 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:105014162..105014528;chr7:105014201..105014579;chr7:105014201..105014526 26863196 MeRIP-seq:(Medium) rs953252278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842969,Human_RBP_ID_5153029,Human_RBP_ID_8653533,Human_RBP_ID_18426549,Human_RBP_ID_23080128,Human_RBP_ID_24181638 63285 RMVar_ID_63285 Human_SNP_ID_333870833 m1A Human chr7 - 105112517 105112517 105112517 GTTTGCTGGCTTGTGGTGCCAGGAAGTGCTTGATTTGGTCCTGATGTAAACACAGTTTGTTGAGA GTTTGCTGGCTTGTGGTGCCAGGAAGTGCTTGGTTTGGTCCTGATGTAAACACAGTTTGTTGAGA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105112466..105112774 26863196 MeRIP-seq:(Medium) rs781265587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17166975,Human_RBP_ID_24181860 63286 RMVar_ID_63286 Human_SNP_ID_333871090 m1A Human chr7 + 105112951 105112951 105112951 GCCACCTTCCAGTGTTTTGGCTTCTGGGCATCATACCACATCAGCTCAAGCCTTACACCACCCAC GCCACCTTCCAGTGTTTTGGCTTCTGGGCATCGTACCACATCAGCTCAAGCCTTACACCACCCAC A G KMT2E Ensembl:ENSG00000005483 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105112901..105113065 26863196 MeRIP-seq:(Medium) rs752566081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17310932,Human_RBP_ID_17538523,Human_RBP_ID_18088144,Human_RBP_ID_18376145,Human_RBP_ID_22111917,Human_RBP_ID_26830696,Human_RBP_ID_27527670 RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602 63287 RMVar_ID_63287 Human_SNP_ID_333871106 m1A Human chr7 - 105112985 105112982 105112985 GCACTCGAAGGAAAAAGTGGAGGTCCTTGATGAGGTGGGTGGTGTAAGGCTTGAGCTGATGTGGT GCACTCGAAGGAAAAAGTGGAGGTCCTTGATG___TGGGTGGTGTAAGGCTTGAGCTGATGTGGT ACCT A SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105112934..105113047 26863196 MeRIP-seq:(Medium) rs1455220409 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_7670712 63288 RMVar_ID_63288 Human_SNP_ID_333871109 m1A Human chr7 - 105112985 105112985 105112985 GCACTCGAAGGAAAAAGTGGAGGTCCTTGATGAGGTGGGTGGTGTAAGGCTTGAGCTGATGTGGT GCACTCGAAGGAAAAAGTGGAGGTCCTTGATGGGGTGGGTGGTGTAAGGCTTGAGCTGATGTGGT T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105112934..105113047 26863196 MeRIP-seq:(Medium) rs770445089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7670712 63289 RMVar_ID_63289 Human_SNP_ID_333900725 m1A Human chr7 + 105223492 105223492 105223492 TCAACCTTGTGTCTTCTACCCTATAAAAAGCCATTCTTCCTTATTTTAGCCAGATTCTACTTTTC TCAACCTTGTGTCTTCTACCCTATAAAAAGCCTTTCTTCCTTATTTTAGCCAGATTCTACTTTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105223487..105223554 26863196 MeRIP-seq:(Medium) rs1275989563 Functional Loss SNV dbSNP153 33..33 33 - - - 63290 RMVar_ID_63290 Human_SNP_ID_333933744 m1A Human chr7 + 105342618 105342618 105342618 CCTGGTCTCACCTCCCAACACTCTCCACAAAGACATTAAACTCAACACATACCAAATTACTTCCA CCTGGTCTCACCTCCCAACACTCTCCACAAAGGCATTAAACTCAACACATACCAAATTACTTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105342616..105342735 26863196 MeRIP-seq:(Medium) rs991004591 Functional Loss SNV dbSNP153 33..33 33 - - - 63291 RMVar_ID_63291 Human_SNP_ID_333944294 m1A Human chr7 + 105377977 105377977 105377977 GGAGCCCCTGGCCTCTAAGCAACTCCCCACACAATAGCTAAAGGAATCTTTCTAAAAACCTGAGT GGAGCCCCTGGCCTCTAAGCAACTCCCCACACGATAGCTAAAGGAATCTTTCTAAAAACCTGAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105377974..105378141 26863196 MeRIP-seq:(Medium) rs1331443421 Functional Loss SNV dbSNP153 33..33 33 - - - 63292 RMVar_ID_63292 Human_SNP_ID_333946725 m1A Human chr7 + 105385590 105385590 105385590 TGACTCCTGCCTCCCATCAACCTCTCTGGGCCACTCAGGCCACTCTTACTTTTGGGTTTCTCGAA TGACTCCTGCCTCCCATCAACCTCTCTGGGCCGCTCAGGCCACTCTTACTTTTGGGTTTCTCGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105385586..105385730 26863196 MeRIP-seq:(Medium) rs577422731 Functional Loss SNV dbSNP153 33..33 33 - - - 63293 RMVar_ID_63293 Human_SNP_ID_333980894 m1A Human chr7 + 105508236 105508236 105508236 GTCTGCAAAACTCTCTGATTCCTCCTCCTCGCACTCCTCTGAAAGTCCATCTTCCTCCTCTTCTT GTCTGCAAAACTCTCTGATTCCTCCTCCTCGCGCTCCTCTGAAAGTCCATCTTCCTCCTCTTCTT A G RF00017-4643,RF00017-4552 RNACentral:URS00009A02E8,RNACentral:URS0000973F83 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105508186..105508395 26863196 MeRIP-seq:(Medium) rs139058270 Functional Loss SNV dbSNP153 33..33 33 - - - 63294 RMVar_ID_63294 Human_SNP_ID_333980895 m1A Human chr7 + 105508236 105508236 105508236 GTCTGCAAAACTCTCTGATTCCTCCTCCTCGCACTCCTCTGAAAGTCCATCTTCCTCCTCTTCTT GTCTGCAAAACTCTCTGATTCCTCCTCCTCGCTCTCCTCTGAAAGTCCATCTTCCTCCTCTTCTT A T RF00017-4643,RF00017-4552 RNACentral:URS00009A02E8,RNACentral:URS0000973F83 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105508186..105508395 26863196 MeRIP-seq:(Medium) rs139058270 Functional Loss SNV dbSNP153 33..33 33 - - - 63295 RMVar_ID_63295 Human_SNP_ID_333980905 m1A Human chr7 - 105508267 105508267 105508267 AAGAATTCTGAGGCTCAGTTGGAAGATGAGGAAGAAGAGGAGGAAGATGGACTTTCAGAGGAGTG AAGAATTCTGAGGCTCAGTTGGAAGATGAGGAGGAAGAGGAGGAAGATGGACTTTCAGAGGAGTG T C PUS7 Ensembl:ENSG00000091127 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:105508163..105508357 26863196 MeRIP-seq:(Medium) rs922596028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1690953,Human_RBP_ID_5480019,Human_RBP_ID_7672006,Human_RBP_ID_8944189,Human_RBP_ID_9311932,Human_RBP_ID_9403810,Human_RBP_ID_22111922,Human_RBP_ID_23080401,Human_RBP_ID_24182445,Human_RBP_ID_24549017,Human_RBP_ID_26356057,Human_RBP_ID_27829727 Human_miRNA_ID_2998386 RMVar_hsa_circ_285289,RMVar_hsa_circ_91963,RMVar_hsa_circ_247583,RMVar_hsa_circ_364623,RMVar_hsa_circ_369206,RMVar_hsa_circ_265423,RMVar_hsa_circ_53467,RMVar_hsa_circ_348168,RMVar_hsa_circ_304172,RMVar_hsa_circ_31559,RMVar_hsa_circ_247622,RMVar_hsa_circ_247611,RMVar_hsa_circ_247612,RMVar_hsa_circ_319086,RMVar_hsa_circ_247623,RMVar_hsa_circ_348278,RMVar_hsa_circ_48350,RMVar_hsa_circ_311814,RMVar_hsa_circ_247625,RMVar_hsa_circ_299525,RMVar_hsa_circ_312992,RMVar_hsa_circ_247626 63296 RMVar_ID_63296 Human_SNP_ID_333988148 m1A Human chr7 - 105532278 105532278 105532278 CTCCGCGCGAGTCCTCGGCTCCATTCGCAGCCAGCGTGGCCTGTGGAGTCTGGCTAAGGCCAGCG CTCCGCGCGAGTCCTCGGCTCCATTCGCAGCCGGCGTGGCCTGTGGAGTCTGGCTAAGGCCAGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105532230..105532847 26863196 MeRIP-seq:(Medium) rs1276648393 Functional Loss SNV dbSNP153 33..33 33 - - - 63297 RMVar_ID_63297 Human_SNP_ID_334017516 m1A Human chr7 - 105643036 105643036 105643036 ATGGTGCCAATGTCAAAATGAACTCCACAACCACTACTGCAGTTTCTGCCTCCTCCACCTCGTCC ATGGTGCCAATGTCAAAATGAACTCCACAACCGCTACTGCAGTTTCTGCCTCCTCCACCTCGTCC T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105642988..105643053 26863196 MeRIP-seq:(Medium) rs895245880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3825481 Human_Splice_Rec_907476,Human_Splice_Rec_907494,Human_Splice_Rec_907520,Human_Splice_Rec_907534,Human_Splice_Rec_907548,Human_Splice_Rec_907558 Human_miRNA_ID_502816,Human_miRNA_ID_510036,Human_miRNA_ID_694581,Human_miRNA_ID_831538,Human_miRNA_ID_1037276,Human_miRNA_ID_1304598,Human_miRNA_ID_2057659,Human_miRNA_ID_2173389,Human_miRNA_ID_2176833,Human_miRNA_ID_2355328,Human_miRNA_ID_2475133 RMVar_hsa_circ_45776,RMVar_hsa_circ_330735,RMVar_hsa_circ_122679,RMVar_hsa_circ_247654,RMVar_hsa_circ_314422,RMVar_hsa_circ_367283,RMVar_hsa_circ_343906,RMVar_hsa_circ_297730,RMVar_hsa_circ_247655,RMVar_hsa_circ_247656,RMVar_hsa_circ_356590 63298 RMVar_ID_63298 Human_SNP_ID_334021403 m1A Human chr7 - 105659725 105659723 105659726 GCCAGGGAGGTATATGGTGTGAGAAGAAGAAGAACAGAGGCCAAGGGTGGTGCCATGGAGGATTG GCCAGGGAGGTATATGGTGTGAGAAGAAGAA___CAGAGGCCAAGGGTGGTGCCATGGAGGATTG GTTC G ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105659688..105659870 26863196 MeRIP-seq:(Medium) rs769274060 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_122679,RMVar_hsa_circ_247654,RMVar_hsa_circ_367283,RMVar_hsa_circ_343906,RMVar_hsa_circ_247656 63299 RMVar_ID_63299 Human_SNP_ID_334040288 m1A Human chr7 - 105733705 105733705 105733705 ATGGATGGAAGGATGGATGGATGGGTGGATGGATGAATGGATGGATGGGTGGATGGGTGGATGGA ATGGATGGAAGGATGGATGGATGGGTGGATGGGTGAATGGATGGATGGGTGGATGGGTGGATGGA T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105733655..105733751 26863196 MeRIP-seq:(Medium) rs1374781307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5657195,Human_RBP_ID_8218496 63300 RMVar_ID_63300 Human_SNP_ID_334040419 m1A Human chr7 - 105733888 105733870 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATG__________________GATGGATGGATGGAT CCATCCATCCATCATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs1563049733 Functional Loss DEL dbSNP153 33..50 33 - - - 63301 RMVar_ID_63301 Human_SNP_ID_334040422 m1A Human chr7 - 105733888 105733874 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATG______________GATGGATGGATGGATGGAT CCATCCATCATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs771092472 Functional Loss DEL dbSNP153 33..46 33 - - - 63302 RMVar_ID_63302 Human_SNP_ID_334040423 m1A Human chr7 - 105733888 105733874 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATG_______ATGGATGGATGGATGGATGGATGGAT CCATCCATCATCCAT CCATCCAT ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs771092472 Functional Loss DEL dbSNP153 33..39 33 - - - 63303 RMVar_ID_63303 Human_SNP_ID_334040428 m1A Human chr7 - 105733888 105733878 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATG__________GATGGATGGATGGATGGATGGAT CCATCATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs1181693391 Functional Loss DEL dbSNP153 33..42 33 - - - 63304 RMVar_ID_63304 Human_SNP_ID_334040443 m1A Human chr7 - 105733888 105733882 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATG______GATGGATGGATGGATGGATGGATGGAT CATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs765532293 Functional Loss DEL dbSNP153 33..38 33 - - - 63305 RMVar_ID_63305 Human_SNP_ID_334040450 m1A Human chr7 - 105733888 105733888 105733888 TGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGGATGGATGGAT TGGATGGATGATGGATGATGGATGGATGGATGGTGGATGATGGATGGATGGATGGATGGATGGAT T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:105733849..105733933 26863196 MeRIP-seq:(Medium) rs1412621046 Functional Loss SNV dbSNP153 33..33 33 - - - 63306 RMVar_ID_63306 Human_SNP_ID_334040466 m1A Human chr7 - 105733917 105733903 105733918 GGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGG GGATGGATGGATGGATGATGGATGATGGATG_______________ATGGATGGATGGATGATGG TCATCCATCATCCATC T ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105733870..105733957 26863196 MeRIP-seq:(Medium) rs1261127667 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_24182564 63307 RMVar_ID_63307 Human_SNP_ID_334040481 m1A Human chr7 - 105733932 105733918 105733932 GATGGATGGATGGATGGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGG GATGGATGGATGGATGGATGGATGGATGGATG______________GATGGATGATGGATGATGG CCATCCATCATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105733903..105733997 26863196 MeRIP-seq:(Medium) rs1324411770 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_24182564 63308 RMVar_ID_63308 Human_SNP_ID_334040482 m1A Human chr7 - 105733932 105733918 105733932 GATGGATGGATGGATGGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGG GATGGATGGATGGATGGATGGATGGATGGATG_______ATGGATGGATGGATGATGGATGATGG CCATCCATCATCCAT CCATCCAT ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105733903..105733997 26863196 MeRIP-seq:(Medium) rs1324411770 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_24182564 63309 RMVar_ID_63309 Human_SNP_ID_334040488 m1A Human chr7 - 105733932 105733926 105733932 GATGGATGGATGGATGGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGG GATGGATGGATGGATGGATGGATGGATGGATG______GATGGATGGATGGATGATGGATGATGG CATCCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105733903..105733997 26863196 MeRIP-seq:(Medium) rs1372664924 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_24182564 63310 RMVar_ID_63310 Human_SNP_ID_334040489 m1A Human chr7 - 105733932 105733929 105733932 GATGGATGGATGGATGGATGGATGGATGGATGATGGATGATGGATGGATGGATGATGGATGATGG GATGGATGGATGGATGGATGGATGGATGGATG___GATGATGGATGGATGGATGATGGATGATGG CCAT C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105733903..105733997 26863196 MeRIP-seq:(Medium) rs1277276432 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_24182564 63311 RMVar_ID_63311 Human_SNP_ID_334063438 m1A Human chr7 - 105833166 105833166 105833166 GGACCTGGGGACCAGCAGATCCAAGGACCCTGAGGCAGGAAGGGGAACATGATAGGGTGGGAGGT GGACCTGGGGACCAGCAGATCCAAGGACCCTGCGGCAGGAAGGGGAACATGATAGGGTGGGAGGT T G ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105833163..105833262 26863196 MeRIP-seq:(Medium) rs1339266560 Functional Loss SNV dbSNP153 33..33 33 - - - 63312 RMVar_ID_63312 Human_SNP_ID_334073380 m1A Human chr7 + 105875861 105875861 105875861 ATAACCTCCCTGCTTTTTCCACCCTCTTTTCCAGCCTCTTCTAAATCTACATCTGCAGATGAAAA ATAACCTCCCTGCTTTTTCCACCCTCTTTTCCGGCCTCTTCTAAATCTACATCTGCAGATGAAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105875783..105875914 26863196 MeRIP-seq:(Medium) rs762658767 Functional Loss SNV dbSNP153 33..33 33 - - - 63313 RMVar_ID_63313 Human_SNP_ID_334073534 m1A Human chr7 + 105876452 105876452 105876452 AGGGTTTGCCCAGAAACGCCTCCGGACTGGGCACTTTGCGATCCAGTGTCGCCATTGCTCTTCCT AGGGTTTGCCCAGAAACGCCTCCGGACTGGGCCCTTTGCGATCCAGTGTCGCCATTGCTCTTCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105876369..105876458 26863196 MeRIP-seq:(Medium) rs1466016086 Functional Loss SNV dbSNP153 33..33 33 - - - 63314 RMVar_ID_63314 Human_SNP_ID_334073535 m1A Human chr7 + 105876452 105876452 105876452 AGGGTTTGCCCAGAAACGCCTCCGGACTGGGCACTTTGCGATCCAGTGTCGCCATTGCTCTTCCT AGGGTTTGCCCAGAAACGCCTCCGGACTGGGCGCTTTGCGATCCAGTGTCGCCATTGCTCTTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105876369..105876458 26863196 MeRIP-seq:(Medium) rs1466016086 Functional Loss SNV dbSNP153 33..33 33 - - - 63315 RMVar_ID_63315 Human_SNP_ID_334073722 m1A Human chr7 + 105876858 105876858 105876858 GAAGGCTGCAGCGCGCCCGGCAGCCGGGATGCAGCGGCGCCGCCCAAGCCTGGGGCGCAGGGGTC GAAGGCTGCAGCGCGCCCGGCAGCCGGGATGCCGCGGCGCCGCCCAAGCCTGGGGCGCAGGGGTC A C CDHR3 Ensembl:ENSG00000128536 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105876808..105876956 26863196 MeRIP-seq:(Medium) rs772674426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4920113,Human_RBP_ID_18426081,Human_RBP_ID_23080689 63316 RMVar_ID_63316 Human_SNP_ID_334106093 m1A Human chr7 + 106012477 106012477 106012477 AGAGCCTCATGAAGAGCTCAGGGAGCACCAGAAGGCCAGAGTGGCAGGAGGAGAGTGAACAAGGA AGAGCCTCATGAAGAGCTCAGGGAGCACCAGAGGGCCAGAGTGGCAGGAGGAGAGTGAACAAGGA A G CDHR3 Ensembl:ENSG00000128536 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:106012430..106012507 26863196 MeRIP-seq:(Medium) rs566225396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55857,RMVar_hsa_circ_247662,RMVar_hsa_circ_247663,RMVar_hsa_circ_377647,RMVar_hsa_circ_1948,RMVar_hsa_circ_247665,RMVar_hsa_circ_23377,RMVar_hsa_circ_310026 63317 RMVar_ID_63317 Human_SNP_ID_334130244 m1A Human chr7 + 106112243 106112243 106112243 TCTGAGGAAAGGAGGGAGAGAGAGTCAGGACGACGGGGCGGAGGAGGGGACCGACGAGACCAGAG TCTGAGGAAAGGAGGGAGAGAGAGTCAGGACGCCGGGGCGGAGGAGGGGACCGACGAGACCAGAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:106112151..106112331 26863196 MeRIP-seq:(Medium) rs1341687517 Functional Loss SNV dbSNP153 33..33 33 - - - 63318 RMVar_ID_63318 Human_SNP_ID_334130245 m1A Human chr7 + 106112243 106112243 106112243 TCTGAGGAAAGGAGGGAGAGAGAGTCAGGACGACGGGGCGGAGGAGGGGACCGACGAGACCAGAG TCTGAGGAAAGGAGGGAGAGAGAGTCAGGACGGCGGGGCGGAGGAGGGGACCGACGAGACCAGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:106112151..106112331 26863196 MeRIP-seq:(Medium) rs1341687517 Functional Loss SNV dbSNP153 33..33 33 - - - 63319 RMVar_ID_63319 Human_SNP_ID_334172558 m1A Human chr7 - 106277176 106277176 106277176 TTCTAACAGAAGTGTATTTCTTTACATAGGTTACTCACTATAAACAATATCCACCCAACACAAGC TTCTAACAGAAGTGTATTTCTTTACATAGGTTCCTCACTATAAACAATATCCACCCAACACAAGC T G NAMPT Ensembl:ENSG00000105835 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:106277151..106277288 26863196 MeRIP-seq:(Medium) rs758957338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956602,Human_RBP_ID_22685801 Human_Splice_Rec_907782,Human_Splice_Rec_907804,Human_Splice_Rec_907828,Human_Splice_Rec_907836,Human_Splice_Rec_907844,Human_Splice_Rec_907852,Human_Splice_Rec_907858,Human_Splice_Rec_907868,Human_Splice_Rec_907872,Human_Splice_Rec_907876 RMVar_hsa_circ_362218 63320 RMVar_ID_63320 Human_SNP_ID_334174836 m1A Human chr7 - 106284951 106284951 106284951 AGTGACTTAAGCAACGGAGCGCGGTGAAGCTCATTTTTCTCCTTCCTCGCAGCCGCGCCAGGGAG AGTGACTTAAGCAACGGAGCGCGGTGAAGCTCGTTTTTCTCCTTCCTCGCAGCCGCGCCAGGGAG T C NAMPT Ensembl:ENSG00000105835 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:106284382..106285114 26863196 MeRIP-seq:(Medium) rs1309648774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956604,Human_RBP_ID_5512429,Human_RBP_ID_17427073,Human_RBP_ID_21405704,Human_RBP_ID_23080142 Human_Splice_Rec_907866 Human_miRNA_ID_1745818 63321 RMVar_ID_63321 Human_SNP_ID_334270255 m1A Human chr7 + 106660730 106660730 106660730 TGCGGGGCATGAAGAGCTTGAAGGCGTCGCCCAGCGCCTTGGTGCTGTCAGCCAGCGACAGTTGC TGCGGGGCATGAAGAGCTTGAAGGCGTCGCCCGGCGCCTTGGTGCTGTCAGCCAGCGACAGTTGC A G lnc-PIK3CG-6 RNACentral:URS00008B4AD6 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:106660679..106660828 32194978 MeRIP-seq:(Medium) rs1371980618 Functional Loss SNV dbSNP153 33..33 33 - - - 63322 RMVar_ID_63322 Human_SNP_ID_334270344 m1A Human chr7 - 106660907 106660907 106660907 GTAGTGGGACCCGGCGAGCGTGAGTGGCCCGGAGCGGCCTTCGATGCGGCGCAGTATGAAGAGGC GTAGTGGGACCCGGCGAGCGTGAGTGGCCCGGGGCGGCCTTCGATGCGGCGCAGTATGAAGAGGC T C AC004917.1,CCDC71L Ensembl:ENSG00000243797,Ensembl:ENSG00000253276 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:106660590..106661150 26863196 MeRIP-seq:(Medium) rs1489250295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956605,Human_RBP_ID_9337335,Human_RBP_ID_27830711 63323 RMVar_ID_63323 Human_SNP_ID_334270371 m1A Human chr7 - 106660957 106660957 106660957 CAGCAGCAGCCGCCGCCGCGGAGCCAACGCGGACTGGGACGGCGGCGGCAGTAGTGGGACCCGGC CAGCAGCAGCCGCCGCCGCGGAGCCAACGCGGCCTGGGACGGCGGCGGCAGTAGTGGGACCCGGC T G AC004917.1,CCDC71L Ensembl:ENSG00000243797,Ensembl:ENSG00000253276 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr7:106660830..106661081;chr7:106660679..106661021 26863196,26863410 MeRIP-seq:(Medium) rs1215703637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956605,Human_RBP_ID_5627730,Human_RBP_ID_7781775 63324 RMVar_ID_63324 Human_SNP_ID_334270414 m1A Human chr7 - 106661028 106661028 106661028 TATTCGCCCGCGTCCTCCGCCCTCGGAGGGGGAGGGGCGGCGGCGGAGGCGAGAAAAGTAGCGAG TATTCGCCCGCGTCCTCCGCCCTCGGAGGGGGGGGGGCGGCGGCGGAGGCGAGAAAAGTAGCGAG T C AC004917.1,CCDC71L Ensembl:ENSG00000243797,Ensembl:ENSG00000253276 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:106660298..106661145 26863196 MeRIP-seq:(Medium) rs555641141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5153279,Human_RBP_ID_5657869 63325 RMVar_ID_63325 Human_SNP_ID_334365142 m1A Human chr7 + 107044914 107044914 107044914 CAGGCGCCTGCCGCCCCGGAGGCAGGATGAGCATCGAGATCCCGGCGGGACTGACGGAGCTGCTG CAGGCGCCTGCCGCCCCGGAGGCAGGATGAGCGTCGAGATCCCGGCGGGACTGACGGAGCTGCTG A G PRKAR2B Ensembl:ENSG00000005249 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107044864..107044952 26863196 MeRIP-seq:(Medium) rs760123694 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4958946,Human_RBP_ID_18108128 63326 RMVar_ID_63326 Human_SNP_ID_334365143 m1A Human chr7 + 107044914 107044914 107044914 CAGGCGCCTGCCGCCCCGGAGGCAGGATGAGCATCGAGATCCCGGCGGGACTGACGGAGCTGCTG CAGGCGCCTGCCGCCCCGGAGGCAGGATGAGCTTCGAGATCCCGGCGGGACTGACGGAGCTGCTG A T PRKAR2B Ensembl:ENSG00000005249 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107044864..107044952 26863196 MeRIP-seq:(Medium) rs760123694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4958946,Human_RBP_ID_18108128 63327 RMVar_ID_63327 Human_SNP_ID_334396417 m1A Human chr7 - 107169062 107169062 107169062 GCCTCCCCCGCGCGGGTTACTGCTCCCGCGGCAGCTCTTACTCCTCAACCGAAACTTTCCTACTT GCCTCCCCCGCGCGGGTTACTGCTCCCGCGGCGGCTCTTACTCCTCAACCGAAACTTTCCTACTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:107169001..107169181;chr7:107169001..107169176;chr7:107169001..107169264;chr7:107169001..107169206 26863196 MeRIP-seq:(Medium) rs779881930 Functional Loss SNV dbSNP153 33..33 33 - - - 63328 RMVar_ID_63328 Human_SNP_ID_334396580 m1A Human chr7 - 107169484 107169484 107169484 CCTTCCCCCGCCCTGGCCCGCCCCATCTCCACACCCGGCCCGGCCACCCACCGCGCGACCTGGCC CCTTCCCCCGCCCTGGCCCGCCCCATCTCCACGCCCGGCCCGGCCACCCACCGCGCGACCTGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107169480..107169631 26863196 MeRIP-seq:(Medium) rs1227480372 Functional Loss SNV dbSNP153 33..33 33 - - - 63329 RMVar_ID_63329 Human_SNP_ID_334398270 m1A Human chr7 + 107174436 107174436 107174436 CTGTTTTGAAATTAAAATAATGTCTTTTTCCAACTTCATTTAAGGAGTTTTGGGATGGTGGTTGA CTGTTTTGAAATTAAAATAATGTCTTTTTCCAGCTTCATTTAAGGAGTTTTGGGATGGTGGTTGA A G HBP1 Ensembl:ENSG00000105856 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:107174431..107174576 26863196 MeRIP-seq:(Medium) rs1228371593 Functional Loss SNV dbSNP153 33..33 33 - - - 63330 RMVar_ID_63330 Human_SNP_ID_334399734 m1A Human chr7 - 107179820 107179820 107179820 TGATGTCAAGCCATGCAATTTGGGCAGTACACAAACCTAAAATAAATCAGAGACATGACAATGTT TGATGTCAAGCCATGCAATTTGGGCAGTACACGAACCTAAAATAAATCAGAGACATGACAATGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:107179817..107179922 26863196 MeRIP-seq:(Medium) rs1413890165 Functional Loss SNV dbSNP153 33..33 33 - - - 63331 RMVar_ID_63331 Human_SNP_ID_334494333 m1A Human chr7 - 107543421 107543421 107543421 CTGGAAGTACTGGCCTGGAGTCGGGCGGGGGCAGCCTGCCCAACACAATTTTAATGGGGCAGGCC CTGGAAGTACTGGCCTGGAGTCGGGCGGGGGCGGCCTGCCCAACACAATTTTAATGGGGCAGGCC T C COG5 Ensembl:ENSG00000164597 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:107543378..107543617 26863196 MeRIP-seq:(Medium) rs1173265612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17169364 RMVar_hsa_circ_10029,RMVar_hsa_circ_95997,RMVar_hsa_circ_247719,RMVar_hsa_circ_22643,RMVar_hsa_circ_2451,RMVar_hsa_circ_316393,RMVar_hsa_circ_341486,RMVar_hsa_circ_320315,RMVar_hsa_circ_314411,RMVar_hsa_circ_247727,RMVar_hsa_circ_247728 63332 RMVar_ID_63332 Human_SNP_ID_334504086 m1A Human chr7 - 107580303 107580303 107580303 GCCCCACGGGTCCCCGGGTCGCAGAAGCCCTTACCCGCCGGCAGCCCGCCTGGCTCCCTGCGCTG GCCCCACGGGTCCCCGGGTCGCAGAAGCCCTTCCCCGCCGGCAGCCCGCCTGGCTCCCTGCGCTG T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:107580288..107580360;chr7:107580290..107580374;chr7:107580285..107580369 26863196 MeRIP-seq:(Medium) rs938593627 Functional Loss SNV dbSNP153 33..33 33 - - - 63333 RMVar_ID_63333 Human_SNP_ID_334552159 m1A Human chr7 + 107758335 107758335 107758335 TCACTTGAAAATGTTCATCCTCCTATTGCCCCACCACCAACTGAAATCCCTGAGCGTTTTATAAT TCACTTGAAAATGTTCATCCTCCTATTGCCCCGCCACCAACTGAAATCCCTGAGCGTTTTATAAT A G CBLL1 Ensembl:ENSG00000105879 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:107758285..107758433 26863196 MeRIP-seq:(Medium) rs747686120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285564,Human_RBP_ID_15971957,Human_RBP_ID_17315343,Human_RBP_ID_22107211 Human_miRNA_ID_863093,Human_miRNA_ID_2377910,Human_miRNA_ID_3092982 RMVar_hsa_circ_107117,RMVar_hsa_circ_247750 63334 RMVar_ID_63334 Human_SNP_ID_334552194 m1A Human chr7 + 107758428 107758428 107758428 ATTCCGCCAAAGCAGCACATCATGATGCCACCACCTCCTTTGCAACATGTGCCACATGAGCACTA ATTCCGCCAAAGCAGCACATCATGATGCCACCCCCTCCTTTGCAACATGTGCCACATGAGCACTA A C CBLL1 Ensembl:ENSG00000105879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:107758379..107758583 26863196 MeRIP-seq:(Medium) rs754835620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1680239,Human_RBP_ID_18088853,Human_RBP_ID_26357009 RMVar_hsa_circ_107117,RMVar_hsa_circ_247750 63335 RMVar_ID_63335 Human_SNP_ID_334589017 m1A Human chr7 - 107891221 107891221 107891221 CATTTTTCCGCTGTATTTTCCTTTCCGCCAATACTTTCACCTCCGCTGGGCGCCTCCGCCGCTCC CATTTTTCCGCTGTATTTTCCTTTCCGCCAATGCTTTCACCTCCGCTGGGCGCCTCCGCCGCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:107891164..107891340;chr7:107891151..107891460 26863196 MeRIP-seq:(Medium) rs1268102432 Functional Loss SNV dbSNP153 33..33 33 - - - 63336 RMVar_ID_63336 Human_SNP_ID_334589019 m1A Human chr7 - 107891223 107891223 107891223 TGCATTTTTCCGCTGTATTTTCCTTTCCGCCAATACTTTCACCTCCGCTGGGCGCCTCCGCCGCT TGCATTTTTCCGCTGTATTTTCCTTTCCGCCAGTACTTTCACCTCCGCTGGGCGCCTCCGCCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:107891151..107891460;chr7:107891176..107891309 26863196 MeRIP-seq:(Medium) rs1219375577 Functional Loss SNV dbSNP153 33..33 33 - - - 63337 RMVar_ID_63337 Human_SNP_ID_334589051 m1A Human chr7 - 107891278 107891278 107891278 CCTCACCTACTCGGCCCTCACCTTGGCCAAGGAGCAGTACACACGACTCCAGCTCTGCATTTTTC CCTCACCTACTCGGCCCTCACCTTGGCCAAGGGGCAGTACACACGACTCCAGCTCTGCATTTTTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:107891176..107891325 26863410 MeRIP-seq:(Medium) rs191765528 Functional Loss SNV dbSNP153 33..33 33 - - - 63338 RMVar_ID_63338 Human_SNP_ID_334589630 m1A Human chr7 - 107893153 107893153 107893153 TGTCCCTATTATGTAAGATATGAATTCAAAACATAGAACTACTGAAGGTTGATGATAACAGAACA TGTCCCTATTATGTAAGATATGAATTCAAAACTTAGAACTACTGAAGGTTGATGATAACAGAACA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107893150..107893275 26863196 MeRIP-seq:(Medium) rs775855092 Functional Loss SNV dbSNP153 33..33 33 - - - 63339 RMVar_ID_63339 Human_SNP_ID_334609197 m1A Human chr7 + 107967354 107967354 107967354 GATGGCATCACCCCATACCTGTTACTCTAACAATCTCCTAAACTGACCTCTCAAATTCTTCTTCC GATGGCATCACCCCATACCTGTTACTCTAACAGTCTCCTAAACTGACCTCTCAAATTCTTCTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107967348..107967423 26863196 MeRIP-seq:(Medium) rs1251627267 Functional Loss SNV dbSNP153 33..33 33 - - - 63340 RMVar_ID_63340 Human_SNP_ID_334611650 m1A Human chr7 - 107976776 107976776 107976776 GAAGATGGGAGGGAGTTCAGGTAAGAACAACAATGTGAAGCACAAGGCCGCAAGGATGTTCTTGA GAAGATGGGAGGGAGTTCAGGTAAGAACAACAGTGTGAAGCACAAGGCCGCAAGGATGTTCTTGA T C LAMB1 Ensembl:ENSG00000091136 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107976767..107976855 26863196 MeRIP-seq:(Medium) rs748973522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111523,RMVar_hsa_circ_247756,RMVar_hsa_circ_326885,RMVar_hsa_circ_113301,RMVar_hsa_circ_102395,RMVar_hsa_circ_247771,RMVar_hsa_circ_247772,RMVar_hsa_circ_247770,RMVar_hsa_circ_9379,RMVar_hsa_circ_82153,RMVar_hsa_circ_9396,RMVar_hsa_circ_247785,RMVar_hsa_circ_87794,RMVar_hsa_circ_247789,RMVar_hsa_circ_106067,RMVar_hsa_circ_342571,RMVar_hsa_circ_64751,RMVar_hsa_circ_109738,RMVar_hsa_circ_247790,RMVar_hsa_circ_247791,RMVar_hsa_circ_100185,RMVar_hsa_circ_247792,RMVar_hsa_circ_247793 63341 RMVar_ID_63341 Human_SNP_ID_334615819 m1A Human chr7 - 107992047 107992047 107992047 ATGTAGATTTGCCTCGAGTTTGGGGTAGTGAGAGAAGGAAAGGAAAGGAAAGTAGAAAAGCAGAT ATGTAGATTTGCCTCGAGTTTGGGGTAGTGAGCGAAGGAAAGGAAAGGAAAGTAGAAAAGCAGAT T G LAMB1 Ensembl:ENSG00000091136 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:107992037..107992135 26863196 MeRIP-seq:(Medium) rs965530143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5220128 RMVar_hsa_circ_111523,RMVar_hsa_circ_247756,RMVar_hsa_circ_326885,RMVar_hsa_circ_102395,RMVar_hsa_circ_247771,RMVar_hsa_circ_247770,RMVar_hsa_circ_9379,RMVar_hsa_circ_82153,RMVar_hsa_circ_9396,RMVar_hsa_circ_247785,RMVar_hsa_circ_87794,RMVar_hsa_circ_247789,RMVar_hsa_circ_106067,RMVar_hsa_circ_64751,RMVar_hsa_circ_247791,RMVar_hsa_circ_100185,RMVar_hsa_circ_247793,RMVar_hsa_circ_362943,RMVar_hsa_circ_247794,RMVar_hsa_circ_323147 63342 RMVar_ID_63342 Human_SNP_ID_334618836 m1A Human chr7 + 108002916 108002901 108002917 ATGCCGGCTCCCTGCAGCCACGGGGACGCGGCAGAGGAGTGGAGAAGACGCCCGCCGAGCCGCCT ATGCCGGCTCCCTGCAGC________________AGGAGTGGAGAAGACGCCCGCCGAGCCGCCT CCACGGGGACGCGGCAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:108002826..108002925 32194978 MeRIP-seq:(Medium) rs1241903411 Functional Loss DEL dbSNP153 19..34 33 - - - 63343 RMVar_ID_63343 Human_SNP_ID_334618862 m1A Human chr7 + 108002941 108002941 108002941 ACGCGGCAGAGGAGTGGAGAAGACGCCCGCCGAGCCGCCTGCCCTTTCTTCCCGTCTTCCTTTCT ACGCGGCAGAGGAGTGGAGAAGACGCCCGCCGCGCCGCCTGCCCTTTCTTCCCGTCTTCCTTTCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:108002896..108003151;chr7:108002896..108002993 26863196 MeRIP-seq:(Medium) rs1018899311 Functional Loss SNV dbSNP153 33..33 33 - - - 63344 RMVar_ID_63344 Human_SNP_ID_334746332 m1A Human chr7 - 108526115 108526115 108526115 AGCTGCTGCGCCAGTGTTTGTGTTGGAAGCTCAGCTGATGCAGGCCGGTTGGAGTGGACGTCATT AGCTGCTGCGCCAGTGTTTGTGTTGGAAGCTCCGCTGATGCAGGCCGGTTGGAGTGGACGTCATT T G PNPLA8 Ensembl:ENSG00000135241 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:108526038..108526268 26863196 MeRIP-seq:(Medium) rs1230771680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956617,Human_RBP_ID_9311441,Human_RBP_ID_18873926 Human_Splice_Rec_910347,Human_Splice_Rec_910365,Human_Splice_Rec_910381,Human_Splice_Rec_910401,Human_Splice_Rec_910417,Human_Splice_Rec_910451,Human_Splice_Rec_910457,Human_Splice_Rec_910473 63345 RMVar_ID_63345 Human_SNP_ID_334756573 m1A Human chr7 - 108569587 108569587 108569587 CCGCCCTGCATCCGTCGCCGGCCCCGGTCTCCAGGGGCCTCACCCGAGTCATGCCCCGCTATTGC CCGCCCTGCATCCGTCGCCGGCCCCGGTCTCCGGGGGCCTCACCCGAGTCATGCCCCGCTATTGC T C PNPLA8,THAP5 Ensembl:ENSG00000135241,Ensembl:ENSG00000177683 Protein coding,Protein coding exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:108569536..108569668 26863196 MeRIP-seq:(Medium) rs1006914303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4921113 Human_Splice_Rec_910469,Human_Splice_Rec_910479,Human_Splice_Rec_910481,Human_Splice_Rec_910489,Human_Splice_Rec_910491,Human_Splice_Rec_910499,Human_Splice_Rec_910505 63346 RMVar_ID_63346 Human_SNP_ID_334756577 m1A Human chr7 + 108569592 108569592 108569592 AGCGGGGCATGACTCGGGTGAGGCCCCTGGAGACCGGGGCCGGCGACGGATGCAGGGCGGCCCTC AGCGGGGCATGACTCGGGTGAGGCCCCTGGAGGCCGGGGCCGGCGACGGATGCAGGGCGGCCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:108569548..108569642;chr7:108569550..108569642 26863196 MeRIP-seq:(Medium) rs1314874528 Functional Loss SNV dbSNP153 33..33 33 - - - 63347 RMVar_ID_63347 Human_SNP_ID_335438840 m1A Human chr7 - 111236078 111236076 111236079 GTTATTGTCACATTTAATTTGTTCAAAAAAGGAGAGGAAAGATTGAAGACATTAAGCACAGAAAT GTTATTGTCACATTTAATTTGTTCAAAAAAG___AGGAAAGATTGAAGACATTAAGCACAGAAAT TCTC T IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:111236053..111236134 26863196 MeRIP-seq:(Medium) rs1392641129 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3042631,Human_RBP_ID_22528900 RMVar_hsa_circ_95445,RMVar_hsa_circ_109595,RMVar_hsa_circ_247831,RMVar_hsa_circ_247832,RMVar_hsa_circ_297778,RMVar_hsa_circ_115148,RMVar_hsa_circ_247833,RMVar_hsa_circ_334358,RMVar_hsa_circ_31692,RMVar_hsa_circ_247834 63348 RMVar_ID_63348 Human_SNP_ID_335447132 m1A Human chr7 - 111271938 111271938 111271938 ATGAGATGACTCTGGTTTAGATTAGTGTGGTAATAGAGATGAAGTAGACAGGTTGGAAACATGTG ATGAGATGACTCTGGTTTAGATTAGTGTGGTAGTAGAGATGAAGTAGACAGGTTGGAAACATGTG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:111271936..111272033 26863196 MeRIP-seq:(Medium) rs1158075412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95445,RMVar_hsa_circ_109595,RMVar_hsa_circ_247831,RMVar_hsa_circ_247832,RMVar_hsa_circ_297778,RMVar_hsa_circ_115148,RMVar_hsa_circ_247833,RMVar_hsa_circ_334358,RMVar_hsa_circ_31692,RMVar_hsa_circ_247834 63349 RMVar_ID_63349 Human_SNP_ID_335518084 m1A Human chr7 - 111556884 111556884 111556884 TATCATTGGCAAGTGTGAGATGTCTAGAAGGCAGTTGGATATAGGATCCTGGAACATCACAAGAG TATCATTGGCAAGTGTGAGATGTCTAGAAGGCGGTTGGATATAGGATCCTGGAACATCACAAGAG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:111556878..111557052 26863196 MeRIP-seq:(Medium) rs1050854268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15977675,Human_RBP_ID_24184564 RMVar_hsa_circ_109595,RMVar_hsa_circ_247832,RMVar_hsa_circ_297778,RMVar_hsa_circ_247833,RMVar_hsa_circ_334358,RMVar_hsa_circ_247842,RMVar_hsa_circ_326034,RMVar_hsa_circ_270816,RMVar_hsa_circ_300300,RMVar_hsa_circ_247844 63350 RMVar_ID_63350 Human_SNP_ID_335518115 m1A Human chr7 - 111556995 111556995 111556995 AATGCTTCCTAGGTTTCTGGGTTGTGAGTGGGAAAAGAGAAGAGGAAGAAGGTATGAGGGAGAAG AATGCTTCCTAGGTTTCTGGGTTGTGAGTGGGTAAAGAGAAGAGGAAGAAGGTATGAGGGAGAAG T A IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:111556979..111557134 26863196 MeRIP-seq:(Medium) rs747074336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070253,Human_RBP_ID_23297503 RMVar_hsa_circ_109595,RMVar_hsa_circ_247832,RMVar_hsa_circ_297778,RMVar_hsa_circ_247833,RMVar_hsa_circ_334358,RMVar_hsa_circ_247842,RMVar_hsa_circ_326034,RMVar_hsa_circ_270816,RMVar_hsa_circ_300300,RMVar_hsa_circ_247844 63351 RMVar_ID_63351 Human_SNP_ID_335518116 m1A Human chr7 - 111556995 111556995 111556995 AATGCTTCCTAGGTTTCTGGGTTGTGAGTGGGAAAAGAGAAGAGGAAGAAGGTATGAGGGAGAAG AATGCTTCCTAGGTTTCTGGGTTGTGAGTGGGGAAAGAGAAGAGGAAGAAGGTATGAGGGAGAAG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:111556979..111557134 26863196 MeRIP-seq:(Medium) rs747074336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070253,Human_RBP_ID_23297503 RMVar_hsa_circ_109595,RMVar_hsa_circ_247832,RMVar_hsa_circ_297778,RMVar_hsa_circ_247833,RMVar_hsa_circ_334358,RMVar_hsa_circ_247842,RMVar_hsa_circ_326034,RMVar_hsa_circ_270816,RMVar_hsa_circ_300300,RMVar_hsa_circ_247844 63352 RMVar_ID_63352 Human_SNP_ID_335592957 m1A Human chr7 - 111850657 111850657 111850657 CAGGAGAAGGAATGTCACAAGGTCAATTGATCAGTTAGGGTGGGGCAGGAACAAATCACAGTGGT CAGGAGAAGGAATGTCACAAGGTCAATTGATCGGTTAGGGTGGGGCAGGAACAAATCACAGTGGT T C DOCK4 Ensembl:ENSG00000128512 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:111850555..111850668 26863196 MeRIP-seq:(Medium) rs576262822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7605,RMVar_hsa_circ_19613,RMVar_hsa_circ_45366,RMVar_hsa_circ_330073,RMVar_hsa_circ_30618,RMVar_hsa_circ_332321,RMVar_hsa_circ_21598,RMVar_hsa_circ_362365,RMVar_hsa_circ_18089,RMVar_hsa_circ_304867,RMVar_hsa_circ_16734,RMVar_hsa_circ_286809,RMVar_hsa_circ_29545,RMVar_hsa_circ_247862,RMVar_hsa_circ_356705,RMVar_hsa_circ_364376,RMVar_hsa_circ_367849,RMVar_hsa_circ_247864,RMVar_hsa_circ_247865 63353 RMVar_ID_63353 Human_SNP_ID_335678287 m1A Human chr7 - 112206353 112206353 112206353 ACTGCGCCGCCGGGTACCCGGGAGCGCGTCGGAGGACTGTGAGCAGCCGCCGCCGGGAGAGCTGC ACTGCGCCGCCGGGTACCCGGGAGCGCGTCGGGGGACTGTGAGCAGCCGCCGCCGGGAGAGCTGC T C DOCK4 Ensembl:ENSG00000128512 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:112206302..112206415 26863196 MeRIP-seq:(Medium) rs1328887782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5533985,Human_RBP_ID_9404846,Human_RBP_ID_18426087,Human_RBP_ID_23080583 63354 RMVar_ID_63354 Human_SNP_ID_335678476 m1A Human chr7 - 112206787 112206787 112206787 CACCGTACTCACCCCCATAACCTACACCCCCGACTGTGCTGCAGCTCCCATCACGGTCTTCCTGC CACCGTACTCACCCCCATAACCTACACCCCCGCCTGTGCTGCAGCTCCCATCACGGTCTTCCTGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:112206736..112206807 26863196 MeRIP-seq:(Medium) rs1447519128 Functional Loss SNV dbSNP153 33..33 33 - - - 63355 RMVar_ID_63355 Human_SNP_ID_335733370 m1A Human chr7 + 112450548 112450548 112450548 GGGGATTTCTGCTGCCGCCACCGCCCACTCTTACCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG GGGGATTTCTGCTGCCGCCACCGCCCACTCTTCCCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG A C IFRD1 Ensembl:ENSG00000006652 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr7:112450464..112450556;chr7:112450501..112450605 26863410,26863196 MeRIP-seq:(Medium) rs1002929425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254084,Human_RBP_ID_673213,Human_RBP_ID_4921450,Human_RBP_ID_5478966,Human_RBP_ID_8655334,Human_RBP_ID_9404849,Human_RBP_ID_18874342,Human_RBP_ID_22463284,Human_RBP_ID_27104078,Human_RBP_ID_27527870 Human_Splice_Rec_911506,Human_Splice_Rec_911508,Human_Splice_Rec_911562 63356 RMVar_ID_63356 Human_SNP_ID_335733371 m1A Human chr7 + 112450548 112450548 112450548 GGGGATTTCTGCTGCCGCCACCGCCCACTCTTACCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG GGGGATTTCTGCTGCCGCCACCGCCCACTCTTGCCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG A G IFRD1 Ensembl:ENSG00000006652 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr7:112450464..112450556;chr7:112450501..112450605 26863410,26863196 MeRIP-seq:(Medium) rs1002929425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254084,Human_RBP_ID_673213,Human_RBP_ID_4921450,Human_RBP_ID_5478966,Human_RBP_ID_8655334,Human_RBP_ID_9404849,Human_RBP_ID_18874342,Human_RBP_ID_22463284,Human_RBP_ID_27104078,Human_RBP_ID_27527870 Human_Splice_Rec_911506,Human_Splice_Rec_911508,Human_Splice_Rec_911562 63357 RMVar_ID_63357 Human_SNP_ID_335812413 m1A Human chr7 + 112789097 112789097 112789097 ACACTTTATTTTCCAACCTTACTGACCTTTCAATTACAAACTGCACAAATGCTATTCCCTTGCCA ACACTTTATTTTCCAACCTTACTGACCTTTCAGTTACAAACTGCACAAATGCTATTCCCTTGCCA A G AC002463.1 Ensembl:ENSG00000223646 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:112789061..112789235 26863196 MeRIP-seq:(Medium) rs895440382 Functional Loss SNV dbSNP153 33..33 33 - - - 63358 RMVar_ID_63358 Human_SNP_ID_335850655 m1A Human chr7 + 112939659 112939657 112939659 TCTTCACCACACCGGAGAGCTTCTCCTGCTCCAGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG TCTTCACCACACCGGAGAGCTTCTCCTGCTC__GTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:112939613..112939773;chr7:112939614..112939758 26863196 MeRIP-seq:(Medium) rs754147676 Functional Loss DEL dbSNP153 32..33 33 - - - 63359 RMVar_ID_63359 Human_SNP_ID_335850656 m1A Human chr7 + 112939659 112939659 112939659 TCTTCACCACACCGGAGAGCTTCTCCTGCTCCAGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG TCTTCACCACACCGGAGAGCTTCTCCTGCTCCCGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:112939613..112939773;chr7:112939614..112939758 26863196 MeRIP-seq:(Medium) rs1187502450 Functional Loss SNV dbSNP153 33..33 33 - - - 63360 RMVar_ID_63360 Human_SNP_ID_335850657 m1A Human chr7 + 112939659 112939659 112939659 TCTTCACCACACCGGAGAGCTTCTCCTGCTCCAGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG TCTTCACCACACCGGAGAGCTTCTCCTGCTCCTGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:112939613..112939773;chr7:112939614..112939758 26863196 MeRIP-seq:(Medium) rs1187502450 Functional Loss SNV dbSNP153 33..33 33 - - - 63361 RMVar_ID_63361 Human_SNP_ID_335850688 m1A Human chr7 + 112939715 112939715 112939715 GGCGGAGTGTTCGGGGACCCGGCCCTCTGCGCACGAGCAGTATTTCGGCCGCCGGCCCCTGGCTC GGCGGAGTGTTCGGGGACCCGGCCCTCTGCGCGCGAGCAGTATTTCGGCCGCCGGCCCCTGGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:112939664..112939800 26863196 MeRIP-seq:(Medium) rs1374882507 Functional Loss SNV dbSNP153 33..33 33 - - - 63362 RMVar_ID_63362 Human_SNP_ID_336128614 m1A Human chr7 + 114088301 114088301 114088301 GGGTGAGTTCTCAGAGGAGGATGGAGGGGGAAAGGGTACGAAGGACCTGTGGGAGTGTGTAAGGT GGGTGAGTTCTCAGAGGAGGATGGAGGGGGAAGGGGTACGAAGGACCTGTGGGAGTGTGTAAGGT A G FOXP2 Ensembl:ENSG00000128573 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:114088296..114088424 26863196 MeRIP-seq:(Medium) rs1007769136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3048158 63363 RMVar_ID_63363 Human_SNP_ID_336243134 m1A Human chr7 - 114562776 114562774 114562776 CTTTCTAATGGCCTAATGATGAAGAAAAAAAAAACAGGGTTAAGATAATTGTCTGATATAAAACT CTTTCTAATGGCCTAATGATGAAGAAAAAAAA__CAGGGTTAAGATAATTGTCTGATATAAAACT GTT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:114562558..114562798 26863196 MeRIP-seq:(Medium) rs5886714 Functional Loss DEL dbSNP153 33..34 33 - - - 63364 RMVar_ID_63364 Human_SNP_ID_336243135 m1A Human chr7 - 114562776 114562774 114562776 CTTTCTAATGGCCTAATGATGAAGAAAAAAAAAACAGGGTTAAGATAATTGTCTGATATAAAACT CTTTCTAATGGCCTAATGATGAAGAAAAAAAA_ACAGGGTTAAGATAATTGTCTGATATAAAACT GTT GT - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:114562558..114562798 26863196 MeRIP-seq:(Medium) rs5886714 Functional Loss DEL dbSNP153 33..33 33 - - - 63365 RMVar_ID_63365 Human_SNP_ID_336334702 m1A Human chr7 - 114922520 114922520 114922520 AGCGGCCGCATTTTCGCCCCGGTGGCCTGACGACGGCGGCGGCCGCCCCTGCGCGTCCTCCCGCC AGCGGCCGCATTTTCGCCCCGGTGGCCTGACGTCGGCGGCGGCCGCCCCTGCGCGTCCTCCCGCC T A lnc-PPP1R3A-4 RNACentral:URS00008B8C52 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:114922252..114923544 26863196 MeRIP-seq:(Medium) rs200906791 Functional Loss SNV dbSNP153 33..33 33 - - - 63366 RMVar_ID_63366 Human_SNP_ID_336334703 m1A Human chr7 - 114922520 114922520 114922520 AGCGGCCGCATTTTCGCCCCGGTGGCCTGACGACGGCGGCGGCCGCCCCTGCGCGTCCTCCCGCC AGCGGCCGCATTTTCGCCCCGGTGGCCTGACGGCGGCGGCGGCCGCCCCTGCGCGTCCTCCCGCC T C lnc-PPP1R3A-4 RNACentral:URS00008B8C52 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:114922252..114923544 26863196 MeRIP-seq:(Medium) rs200906791 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 63367 RMVar_ID_63367 Human_SNP_ID_336334751 m1A Human chr7 + 114922614 114922614 114922614 AAGAGGAGGAGGAGGAGGAGGAAGGGGCTTGGAGCGACTACGGGGGGATGCGGAGGTAGGTAGTG AAGAGGAGGAGGAGGAGGAGGAAGGGGCTTGGCGCGACTACGGGGGGATGCGGAGGTAGGTAGTG A C MDFIC Ensembl:ENSG00000135272 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:114922253..114922669;chr7:114922252..114923544 26863196 MeRIP-seq:(Medium) rs1440355937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7682340,Human_RBP_ID_18090070,Human_RBP_ID_24185781 Human_Splice_Rec_913239,Human_Splice_Rec_913247,Human_Splice_Rec_913255 63368 RMVar_ID_63368 Human_SNP_ID_336334853 m1A Human chr7 + 114922892 114922891 114922893 CCCGCAGGGGTGGTGTGCTCTTCTCTAAAAACATTTTTTTTTTTAATTTTGTATATTTTTCCGCC CCCGCAGGGGTGGTGTGCTCTTCTCTAAAAAC__TTTTTTTTTTAATTTTGTATATTTTTCCGCC CAT C MDFIC Ensembl:ENSG00000135272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:114922889..114923158 26863196 MeRIP-seq:(Medium) rs1491421206 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7682342 63369 RMVar_ID_63369 Human_SNP_ID_336343813 m1A Human chr7 + 114961401 114961401 114961401 ATTGTCACTAGTAGCAGCCCTGAGCTCCTGACACCAGGCTGAAAGCAGAGGGGATTATGACACTA ATTGTCACTAGTAGCAGCCCTGAGCTCCTGACGCCAGGCTGAAAGCAGAGGGGATTATGACACTA A G MDFIC Ensembl:ENSG00000135272 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:114942204..114979600 26863196 MeRIP-seq:(Medium) rs1195410789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247927,RMVar_hsa_circ_321753,RMVar_hsa_circ_336559 63370 RMVar_ID_63370 Human_SNP_ID_336655502 m1A Human chr7 - 116210709 116210709 116210709 CCCCTACCTTCTTCACTTTGTTTTCCAGGTCCATGTTAACGCGTCCTATGGGTCCCCTCCTCCTC CCCCTACCTTCTTCACTTTGTTTTCCAGGTCCGTGTTAACGCGTCCTATGGGTCCCCTCCTCCTC T C AC073130.3 Ensembl:ENSG00000279086 Other exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:116210551..116210799 26863196 MeRIP-seq:(Medium) rs574841607 Functional Loss SNV dbSNP153 33..33 33 - - - 63371 RMVar_ID_63371 Human_SNP_ID_336655503 m1A Human chr7 - 116210709 116210709 116210709 CCCCTACCTTCTTCACTTTGTTTTCCAGGTCCATGTTAACGCGTCCTATGGGTCCCCTCCTCCTC CCCCTACCTTCTTCACTTTGTTTTCCAGGTCCCTGTTAACGCGTCCTATGGGTCCCCTCCTCCTC T G AC073130.3 Ensembl:ENSG00000279086 Other exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:116210551..116210799 26863196 MeRIP-seq:(Medium) rs574841607 Functional Loss SNV dbSNP153 33..33 33 - - - 63372 RMVar_ID_63372 Human_SNP_ID_336664631 m1A Human chr7 + 116250236 116250236 116250236 TAGCAGGCTCAGAGGGGGCACAGTACCGGAAGAAGCAGCTGGCAAAGCAGCTCCCTGCACATGAC TAGCAGGCTCAGAGGGGGCACAGTACCGGAAGCAGCAGCTGGCAAAGCAGCTCCCTGCACATGAC A C TES Ensembl:ENSG00000135269 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:116250185..116250397 26863196 MeRIP-seq:(Medium) rs148268755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090589,Human_RBP_ID_7682915 Human_Splice_Rec_913440,Human_Splice_Rec_913446,Human_Splice_Rec_913468 RMVar_hsa_circ_352448,RMVar_hsa_circ_365560,RMVar_hsa_circ_247929 63373 RMVar_ID_63373 Human_SNP_ID_336708471 m1A Human chr7 - 116430353 116430344 116430354 AGAGAGACAGGGAGAGAGAGAGAGAGAGAAAGAGAGAGAAAAACAGAGAGAGAGAGAGGGAGAGA AGAGAGACAGGGAGAGAGAGAGAGAGAGAAA__________AACAGAGAGAGAGAGAGGGAGAGA TTTTCTCTCTC T AC002066.1 Ensembl:ENSG00000237813 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116430303..116430514 26863196 MeRIP-seq:(Medium) rs1341540698 Functional Loss DEL dbSNP153 32..41 33 - - - 63374 RMVar_ID_63374 Human_SNP_ID_336724608 m1A Human chr7 + 116499873 116499873 116499873 CCACCACAGCGGCCTCGAGTACGCCGACCCCGAGAAGTTCGCGGACTCGGACCAGGACCGGGATC CCACCACAGCGGCCTCGAGTACGCCGACCCCGGGAAGTTCGCGGACTCGGACCAGGACCGGGATC A G CAV2 Ensembl:ENSG00000105971 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:116499655..116500001 26863196 MeRIP-seq:(Medium) rs762743961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956630,Human_RBP_ID_5153291,Human_RBP_ID_23080150 Human_Splice_Rec_913596,Human_Splice_Rec_913597,Human_Splice_Rec_913634,Human_Splice_Rec_913635,Human_Splice_Rec_913670,Human_Splice_Rec_913671,Human_Splice_Rec_913683,Human_Splice_Rec_913687,Human_Splice_Rec_913689 RMVar_hsa_circ_107448,RMVar_hsa_circ_247932 63375 RMVar_ID_63375 Human_SNP_ID_336724752 m1A Human chr7 + 116500278 116500278 116500278 TCCTGTCTCCTCAGCTGGGCTTCGAGGATGTGATCGCAGAGCCGGTGACTACGCACTCCTTTGAC TCCTGTCTCCTCAGCTGGGCTTCGAGGATGTGTTCGCAGAGCCGGTGACTACGCACTCCTTTGAC A T CAV2 Ensembl:ENSG00000105971 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116500251..116500350 32194978 MeRIP-seq:(Medium) rs1280293557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_673539,Human_RBP_ID_4956631,Human_RBP_ID_5512495,Human_RBP_ID_7683054 Human_Splice_Rec_913598,Human_Splice_Rec_913636,Human_Splice_Rec_913672,Human_Splice_Rec_913684,Human_Splice_Rec_913690 Human_miRNA_ID_2395068,Human_miRNA_ID_2395069,Human_miRNA_ID_3068746,Human_miRNA_ID_3068747 RMVar_hsa_circ_107448,RMVar_hsa_circ_369749,RMVar_hsa_circ_247932,RMVar_hsa_circ_247933 63376 RMVar_ID_63376 Human_SNP_ID_336725683 m1A Human chr7 + 116503979 116503979 116503979 AAGACAGAAAGAAAAAGAGAAAGAAGGAAAGAAAGAAAGAAAAGAAGAAAGAAAAAAGAAAAGAA AAGACAGAAAGAAAAAGAGAAAGAAGGAAAGAGAGAAAGAAAAGAAGAAAGAAAAAAGAAAAGAA A G CAV2 Ensembl:ENSG00000105971 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:116503958..116504059 26863196 MeRIP-seq:(Medium) rs1456121473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14008 63377 RMVar_ID_63377 Human_SNP_ID_336730885 m1A Human chr7 + 116525077 116525077 116525077 ATCCAGCCACGGGCCAGCATGTCTGGGGGCAAATACGTAGACTCGGAGGTAGGCATCCGTGGGGG ATCCAGCCACGGGCCAGCATGTCTGGGGGCAAGTACGTAGACTCGGAGGTAGGCATCCGTGGGGG A G CAV1 Ensembl:ENSG00000105974 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116525026..116525100 32194978 MeRIP-seq:(Medium) rs1230681045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_913693,Human_Splice_Rec_913705,Human_Splice_Rec_913707 63378 RMVar_ID_63378 Human_SNP_ID_336731446 m1A Human chr7 + 116526571 116526571 116526571 CGTTCCCATCCGGGAACAGGGCAACATCTACAAGCCCAACAACAAGGCCATGGCAGACGAGCTGA CGTTCCCATCCGGGAACAGGGCAACATCTACAGGCCCAACAACAAGGCCATGGCAGACGAGCTGA A G CAV1 Ensembl:ENSG00000105974 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116526419..116526719 32194978 MeRIP-seq:(Medium) rs1231263155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_913694,Human_Splice_Rec_913698,Human_Splice_Rec_913702,Human_Splice_Rec_913706,Human_Splice_Rec_913708,Human_Splice_Rec_913712,Human_Splice_Rec_913716,Human_Splice_Rec_913720 RMVar_hsa_circ_4283 63379 RMVar_ID_63379 Human_SNP_ID_336739769 m1A Human chr7 - 116559442 116559439 116559442 AAAAATAGATGAAATAGCTCAGAAGAGACATAATACTTATGAAAACTGAGAAAGTGATCTTTTTA AAAAATAGATGAAATAGCTCAGAAGAGACATA___CTTATGAAAACTGAGAAAGTGATCTTTTTA GTAT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116559242..116559442 32194978 MeRIP-seq:(Medium) rs1256498817 Functional Loss DEL dbSNP153 33..35 33 - - - 63380 RMVar_ID_63380 Human_SNP_ID_336739770 m1A Human chr7 - 116559442 116559442 116559442 AAAAATAGATGAAATAGCTCAGAAGAGACATAATACTTATGAAAACTGAGAAAGTGATCTTTTTA AAAAATAGATGAAATAGCTCAGAAGAGACATAGTACTTATGAAAACTGAGAAAGTGATCTTTTTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116559242..116559442 32194978 MeRIP-seq:(Medium) rs1226658948 Functional Loss SNV dbSNP153 33..33 33 - - - 63381 RMVar_ID_63381 Human_SNP_ID_336767045 m1A Human chr7 - 116672438 116672438 116672438 CTCGCGCCCTCCACTCGGCTCCGCATCTGCTCACAAAGCGCTCGGGGCGCCGCGGGCGGCGAGGG CTCGCGCCCTCCACTCGGCTCCGCATCTGCTCGCAAAGCGCTCGGGGCGCCGCGGGCGGCGAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:116672035..116672575 26863196 MeRIP-seq:(Medium) rs1263050872 Functional Loss SNV dbSNP153 33..33 33 - - - 63382 RMVar_ID_63382 Human_SNP_ID_336780957 m1A Human chr7 + 116730506 116730506 116730506 CAGTGTGAAGAACAGATCACCTGGCAAGGGTAACAGTGGATGTGGTGGGTCTAGTTAAGAAGCCG CAGTGTGAAGAACAGATCACCTGGCAAGGGTAGCAGTGGATGTGGTGGGTCTAGTTAAGAAGCCG A G MET Ensembl:ENSG00000105976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116730495..116730647 26863196 MeRIP-seq:(Medium) rs1257811340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124371,RMVar_hsa_circ_278580,RMVar_hsa_circ_362941,RMVar_hsa_circ_247936,RMVar_hsa_circ_247937,RMVar_hsa_circ_353168 63383 RMVar_ID_63383 Human_SNP_ID_336786715 m1A Human chr7 + 116754865 116754856 116754866 AAAGAAGGAAGAAAGGAAGGGAGGGAAAGAAAAAGAAAGAAAGAGAGAGAGAGAGAAAGAGAGAA AAAGAAGGAAGAAAGGAAGGGAGG__________GAAAGAAAGAGAGAGAGAGAGAAAGAGAGAA GGAAAGAAAAA G MET Ensembl:ENSG00000105976 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:116754823..116755029;chr7:116754860..116754986 26863196 MeRIP-seq:(Medium) rs1274362652 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_26065314 RMVar_hsa_circ_2600,RMVar_hsa_circ_124371,RMVar_hsa_circ_247937,RMVar_hsa_circ_88002,RMVar_hsa_circ_56171,RMVar_hsa_circ_91038,RMVar_hsa_circ_247938,RMVar_hsa_circ_70499,RMVar_hsa_circ_68582,RMVar_hsa_circ_247939,RMVar_hsa_circ_51032 63384 RMVar_ID_63384 Human_SNP_ID_336786715 m1A Human chr7 + 116754866 116754856 116754866 AAGAAGGAAGAAAGGAAGGGAGGGAAAGAAAAAGAAAGAAAGAGAGAGAGAGAGAAAGAGAGAAA AAGAAGGAAGAAAGGAAGGGAGG__________GAAAGAAAGAGAGAGAGAGAGAAAGAGAGAAA GGAAAGAAAAA G MET Ensembl:ENSG00000105976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116754861..116754997 26863196 MeRIP-seq:(Medium) rs1274362652 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_26065314 RMVar_hsa_circ_2600,RMVar_hsa_circ_124371,RMVar_hsa_circ_247937,RMVar_hsa_circ_88002,RMVar_hsa_circ_56171,RMVar_hsa_circ_91038,RMVar_hsa_circ_247938,RMVar_hsa_circ_70499,RMVar_hsa_circ_68582,RMVar_hsa_circ_247939,RMVar_hsa_circ_51032 63385 RMVar_ID_63385 Human_SNP_ID_336786717 m1A Human chr7 + 116754866 116754863 116754867 AAGAAGGAAGAAAGGAAGGGAGGGAAAGAAAAAGAAAGAAAGAGAGAGAGAGAGAAAGAGAGAAA AAGAAGGAAGAAAGGAAGGGAGGGAAAGAA____AAAGAAAGAGAGAGAGAGAGAAAGAGAGAAA AAAAG A MET Ensembl:ENSG00000105976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116754861..116754997 26863196 MeRIP-seq:(Medium) rs1489785801 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_26065314 RMVar_hsa_circ_2600,RMVar_hsa_circ_124371,RMVar_hsa_circ_247937,RMVar_hsa_circ_88002,RMVar_hsa_circ_56171,RMVar_hsa_circ_91038,RMVar_hsa_circ_247938,RMVar_hsa_circ_70499,RMVar_hsa_circ_68582,RMVar_hsa_circ_247939,RMVar_hsa_circ_51032 63386 RMVar_ID_63386 Human_SNP_ID_336812485 m1A Human chr7 - 116862574 116862571 116862574 TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCAGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT TTCTGGCGACAAACCGCGGCGGCGGCGGCGGC___GGCCACCTGACTTCCCCGTTTCCGTGCGGT CGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:116862526..116862699 26863196 MeRIP-seq:(Medium) rs754710280 Functional Loss DEL dbSNP153 33..35 33 - - - 63387 RMVar_ID_63387 Human_SNP_ID_336812489 m1A Human chr7 - 116862574 116862574 116862574 TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCAGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCGGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:116862526..116862699 26863196 MeRIP-seq:(Medium) rs192510686 Functional Loss SNV dbSNP153 33..33 33 - - - 63388 RMVar_ID_63388 Human_SNP_ID_336826280 m1A Human chr7 + 116918194 116918194 116918194 AAAATATTTTACTAACTGTAACCCTAAAATTGATGTCTTTTGGTTTATGAAATCAGTAATTTTTG AAAATATTTTACTAACTGTAACCCTAAAATTGGTGTCTTTTGGTTTATGAAATCAGTAATTTTTG A G CAPZA2 Ensembl:ENSG00000198898 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:116918060..116918211 32194978 MeRIP-seq:(Medium) rs1562965175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2033928,Human_RBP_ID_3828973 Human_miRNA_ID_1042437,Human_miRNA_ID_2480915,Human_miRNA_ID_2951799 RMVar_hsa_circ_92573,RMVar_hsa_circ_247945 63389 RMVar_ID_63389 Human_SNP_ID_336835274 m1A Human chr7 - 116953535 116953534 116953535 CAGAAAGCCCGTGGCCGCTTCAGCCATGTTTCAGCGCTCCTCTCTGCTGCCGCGGCTCTTGGTGT CAGAAAGCCCGTGGCCGCTTCAGCCATGTTTC_GCGCTCCTCTCTGCTGCCGCGGCTCTTGGTGT CT C ST7-AS1 Ensembl:ENSG00000227199 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116953438..116953535 26863196 MeRIP-seq:(Medium) rs1479558833 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22111959 63390 RMVar_ID_63390 Human_SNP_ID_336842838 m1A Human chr7 + 116986236 116986236 116986236 TTGAAAGTGGGATGATTCTGCTGTTTCATTCTAACTGTAAGTGGAAAGGAGGGGAGGAGATGGGA TTGAAAGTGGGATGATTCTGCTGTTTCATTCTGACTGTAAGTGGAAAGGAGGGGAGGAGATGGGA A G ST7,ST7-OT4 Ensembl:ENSG00000004866,Ensembl:ENSG00000214188 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:116986227..116986338 26863196 MeRIP-seq:(Medium) rs928371600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7683750 63391 RMVar_ID_63391 Human_SNP_ID_336895780 m1A Human chr7 - 117229901 117229901 117229901 CTTGCGGTCCACAAGGAGTTGGCACAGAGGAGATGGTGGCAGCGGCGGGTGAGGTGAGTGGAGGA CTTGCGGTCCACAAGGAGTTGGCACAGAGGAGTTGGTGGCAGCGGCGGGTGAGGTGAGTGGAGGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:117229850..117229925 26863196 MeRIP-seq:(Medium) rs373570413 Functional Loss SNV dbSNP153 33..33 33 - - - 63392 RMVar_ID_63392 Human_SNP_ID_4100733 m1A Human chr1 + 15220329 15220329 15220329 CTTAAGGCCTGATGAACGTAGGCACGTGATGCATAATAGTCTTCAATGGTACACTTAACTAGTCT CTTAAGGCCTGATGAACGTAGGCACGTGATGCCTAATAGTCTTCAATGGTACACTTAACTAGTCT A C TMEM51 Ensembl:ENSG00000171729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328199 GWAS_ID_7719,GWAS_ID_7720,GWAS_ID_7721,GWAS_ID_7722,GWAS_ID_7723,GWAS_ID_7724 63393 RMVar_ID_63393 Human_SNP_ID_4100734 m1A Human chr1 + 15220329 15220329 15220329 CTTAAGGCCTGATGAACGTAGGCACGTGATGCATAATAGTCTTCAATGGTACACTTAACTAGTCT CTTAAGGCCTGATGAACGTAGGCACGTGATGCGTAATAGTCTTCAATGGTACACTTAACTAGTCT A G TMEM51 Ensembl:ENSG00000171729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328199 GWAS_ID_7719,GWAS_ID_7720,GWAS_ID_7721,GWAS_ID_7722,GWAS_ID_7723,GWAS_ID_7724 63394 RMVar_ID_63394 Human_SNP_ID_4100735 m1A Human chr1 + 15220329 15220329 15220329 CTTAAGGCCTGATGAACGTAGGCACGTGATGCATAATAGTCTTCAATGGTACACTTAACTAGTCT CTTAAGGCCTGATGAACGTAGGCACGTGATGCTTAATAGTCTTCAATGGTACACTTAACTAGTCT A T TMEM51 Ensembl:ENSG00000171729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328199 GWAS_ID_7719,GWAS_ID_7720,GWAS_ID_7721,GWAS_ID_7722,GWAS_ID_7723,GWAS_ID_7724 63395 RMVar_ID_63395 Human_SNP_ID_4125515 m1A Human chr1 - 15323273 15323273 15323273 CTGGCCTCCCCGCCCCCAGCCCCAGCTCTGGCAGTCCTGTTCTTCATATCACTGCCACACAGCAG CTGGCCTCCCCGCCCCCAGCCCCAGCTCTGGCGGTCCTGTTCTTCATATCACTGCCACACAGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15323231..15323358 26863196 MeRIP-seq:(Medium) rs1179878895 Functional Loss SNV dbSNP153 33..33 33 - - - 63396 RMVar_ID_63396 Human_SNP_ID_4148152 m1A Human chr1 + 15409948 15409948 15409948 GGCGGCGCTGCGCTGAGAGCAGGGGCCCGGCCAAGGCGAGTGCCGCGCGGGCCACCATGGCCACG GGCGGCGCTGCGCTGAGAGCAGGGGCCCGGCCGAGGCGAGTGCCGCGCGGGCCACCATGGCCACG A G EFHD2 Ensembl:ENSG00000142634 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:15409876..15410320 26863196 MeRIP-seq:(Medium) rs1161161668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073577,Human_RBP_ID_17727733 63397 RMVar_ID_63397 Human_SNP_ID_4153447 m1A Human chr1 + 15428927 15428927 15428927 CCCCGCTCCCTTCCACTCTGCACGAGGCCGCCACACCGGCGCTGGCTCCCTGCCCGGCCCGGCCC CCCCGCTCCCTTCCACTCTGCACGAGGCCGCCGCACCGGCGCTGGCTCCCTGCCCGGCCCGGCCC A G EFHD2 Ensembl:ENSG00000142634 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:15428876..15428975 32194978 MeRIP-seq:(Medium) rs888548217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329231,Human_RBP_ID_23337307,Human_RBP_ID_27389683 63398 RMVar_ID_63398 Human_SNP_ID_4178719 m1A Human chr1 + 15524151 15524151 15524151 CGTCCCAGAGCTGGTCCACCTGCAGCTCTTCCACCAGCCGCAGCCGGCACCGCCGCAGGAGCCGC CGTCCCAGAGCTGGTCCACCTGCAGCTCTTCCCCCAGCCGCAGCCGGCACCGCCGCAGGAGCCGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15524037..15524448 26863196 MeRIP-seq:(Medium) rs766813971 Functional Loss SNV dbSNP153 33..33 33 - - - 63399 RMVar_ID_63399 Human_SNP_ID_4179779 m1A Human chr1 + 15527081 15527081 15527081 GTCACTGCTGGCCCCGGGGGGAGCCGGGAGCCAACAGGGCCGGGCCCTGGGCTCTCGGAGGGCGG GTCACTGCTGGCCCCGGGGGGAGCCGGGAGCCTACAGGGCCGGGCCCTGGGCTCTCGGAGGGCGG A T DNAJC16 Ensembl:ENSG00000116138 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:15526887..15527209 26863196 MeRIP-seq:(Medium) rs1173606899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5336972 63400 RMVar_ID_63400 Human_SNP_ID_4221331 m1A Human chr1 - 15684525 15684522 15684525 GCGCTGCCACCGTCGCCGCCACCGCCACCGCCACCGCCGCCGCCGCCCCGCCGCCGCTTCCCGCG GCGCTGCCACCGTCGCCGCCACCGCCACCGCC___GCCGCCGCCGCCCCGCCGCCGCTTCCCGCG CGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:15684390..15684540 26863196 MeRIP-seq:(Medium) rs758579555 Functional Loss DEL dbSNP153 33..35 33 - - - 63401 RMVar_ID_63401 Human_SNP_ID_4221334 m1A Human chr1 - 15684525 15684525 15684525 GCGCTGCCACCGTCGCCGCCACCGCCACCGCCACCGCCGCCGCCGCCCCGCCGCCGCTTCCCGCG GCGCTGCCACCGTCGCCGCCACCGCCACCGCCGCCGCCGCCGCCGCCCCGCCGCCGCTTCCCGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:15684390..15684540 26863196 MeRIP-seq:(Medium) rs778195790 Functional Loss SNV dbSNP153 33..33 33 - - - 63402 RMVar_ID_63402 Human_SNP_ID_4221335 m1A Human chr1 - 15684525 15684525 15684525 GCGCTGCCACCGTCGCCGCCACCGCCACCGCCACCGCCGCCGCCGCCCCGCCGCCGCTTCCCGCG GCGCTGCCACCGTCGCCGCCACCGCCACCGCCCCCGCCGCCGCCGCCCCGCCGCCGCTTCCCGCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:15684390..15684540 26863196 MeRIP-seq:(Medium) rs778195790 Functional Loss SNV dbSNP153 33..33 33 - - - 63403 RMVar_ID_63403 Human_SNP_ID_4232249 m1A Human chr1 - 15727572 15727572 15727572 CCCTCTCCTCCTCCTCCCTCTTCTTCTTGGCCAGCAGCCTCAGGGCTACTAGGAACATGCAGCGG CCCTCTCCTCCTCCTCCCTCTTCTTCTTGGCCTGCAGCCTCAGGGCTACTAGGAACATGCAGCGG T A AL450998.3 Ensembl:ENSG00000237938 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:15727523..15727748 26863196 MeRIP-seq:(Medium) rs745792439 Functional Loss SNV dbSNP153 33..33 33 - - - 63404 RMVar_ID_63404 Human_SNP_ID_4233323 m1A Human chr1 + 15730621 15730621 15730621 GAGTCCCTGGGCCCCACGCCCTGCCACTGCTCACCCCCCGAGGGCACCATCACCAAAGAAGGCAT GAGTCCCTGGGCCCCACGCCCTGCCACTGCTCGCCCCCCGAGGGCACCATCACCAAAGAAGGCAT A G PLEKHM2 Ensembl:ENSG00000116786 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:15730571..15730650 26863196 MeRIP-seq:(Medium) rs1557662660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21086,Human_Splice_Rec_21122,Human_Splice_Rec_21168,Human_Splice_Rec_21180 RMVar_hsa_circ_99835,RMVar_hsa_circ_91755,RMVar_hsa_circ_129434,RMVar_hsa_circ_129435,RMVar_hsa_circ_119985,RMVar_hsa_circ_82933,RMVar_hsa_circ_86345,RMVar_hsa_circ_129437,RMVar_hsa_circ_129438,RMVar_hsa_circ_129436,RMVar_hsa_circ_99319,RMVar_hsa_circ_129446,RMVar_hsa_circ_120319,RMVar_hsa_circ_94860,RMVar_hsa_circ_118199,RMVar_hsa_circ_123961,RMVar_hsa_circ_129453,RMVar_hsa_circ_129454,RMVar_hsa_circ_129456,RMVar_hsa_circ_114598,RMVar_hsa_circ_129455,RMVar_hsa_circ_79293,RMVar_hsa_circ_129457,RMVar_hsa_circ_97986,RMVar_hsa_circ_129458,RMVar_hsa_circ_129459 63405 RMVar_ID_63405 Human_SNP_ID_4238021 m1A Human chr1 + 15745521 15745514 15745522 AGCCTGGGCGACAGAGAGAGATTCTGGAAAGAAAGAAAGAGAGAAAGAGAGAGAGAAAGAGAGAA AGCCTGGGCGACAGAGAGAGATTCTG________GAAAGAGAGAAAGAGAGAGAGAAAGAGAGAA GGAAAGAAA G TMEM82 Ensembl:ENSG00000162460 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15745515..15745580 26863196 MeRIP-seq:(Medium) rs1330099320 Functional Loss DEL dbSNP153 27..34 33 - - - 63406 RMVar_ID_63406 Human_SNP_ID_4243243 m1A Human chr1 + 15764576 15764576 15764576 CCAGGTGAGGGAGGTCACTTGGGGTGTGGCCCAGCAGGCAGGCGGGACTCCAGACTGGGAACGGA CCAGGTGAGGGAGGTCACTTGGGGTGTGGCCCCGCAGGCAGGCGGGACTCCAGACTGGGAACGGA A C FBLIM1 Ensembl:ENSG00000162458 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:15764503..15764612 26863196 MeRIP-seq:(Medium) rs1201317523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19033980 Human_Splice_Rec_21244,Human_Splice_Rec_21250,Human_Splice_Rec_21254,Human_Splice_Rec_21260,Human_Splice_Rec_21266,Human_Splice_Rec_21284,Human_Splice_Rec_21290,Human_Splice_Rec_21294,Human_Splice_Rec_21300,Human_Splice_Rec_21308,Human_Splice_Rec_21324 Human_miRNA_ID_2510141,Human_miRNA_ID_3052962 RMVar_hsa_circ_11681,RMVar_hsa_circ_111218,RMVar_hsa_circ_127998,RMVar_hsa_circ_109707,RMVar_hsa_circ_129464,RMVar_hsa_circ_129465,RMVar_hsa_circ_81041,RMVar_hsa_circ_129466,RMVar_hsa_circ_297739,RMVar_hsa_circ_37178,RMVar_hsa_circ_42247,RMVar_hsa_circ_304938,RMVar_hsa_circ_129467,RMVar_hsa_circ_337837,RMVar_hsa_circ_42899,RMVar_hsa_circ_129468 63407 RMVar_ID_63407 Human_SNP_ID_4249032 m1A Human chr1 + 15785925 15785925 15785925 CACCTCCCGGGTGCTGTGTTGAGTCAGCAGGCATGGGGTGAGAGCCTGGTATATGCTGGGAACAG CACCTCCCGGGTGCTGTGTTGAGTCAGCAGGCGTGGGGTGAGAGCCTGGTATATGCTGGGAACAG A G FBLIM1 Ensembl:ENSG00000162458 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:15785849..15785949 32194978 MeRIP-seq:(Medium) rs985787083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1696757 RMVar_hsa_circ_111218,RMVar_hsa_circ_127998,RMVar_hsa_circ_109707,RMVar_hsa_circ_129464,RMVar_hsa_circ_129465,RMVar_hsa_circ_81041,RMVar_hsa_circ_129466,RMVar_hsa_circ_129467,RMVar_hsa_circ_125412,RMVar_hsa_circ_90372,RMVar_hsa_circ_109564,RMVar_hsa_circ_129476,RMVar_hsa_circ_129478,RMVar_hsa_circ_113146,RMVar_hsa_circ_129479,RMVar_hsa_circ_129480 63408 RMVar_ID_63408 Human_SNP_ID_4254839 m1A Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCGAAGGACCATTGCGTGGCCCACAAACTCTTTAA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10722 Functional Loss SNV dbSNP153 33..33 33 - - - 63409 RMVar_ID_63409 Human_SNP_ID_4254840 m1A Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCCAAGGACCATTGCGTGGCCCACAAACTCTTTAA T G UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10722 Functional Loss SNV dbSNP153 33..33 33 - - - 63410 RMVar_ID_63410 Human_SNP_ID_4254938 m1A Human chr1 + 15807621 15807621 15807621 CTTCCTCCTCCTCAGGATCTCCGGATTCGGTAAGCATCTTTTGCTCGTCCTCCAGTCCCATGTCT CTTCCTCCTCCTCAGGATCTCCGGATTCGGTAGGCATCTTTTGCTCGTCCTCCAGTCCCATGTCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:15807564..15807664 26863410 MeRIP-seq:(Medium) rs1312278838 Functional Loss SNV dbSNP153 33..33 33 - - - 63411 RMVar_ID_63411 Human_SNP_ID_4263066 m1A Human chr1 - 15835690 15835689 15835690 ACCCAAGCGCACCGCGACACCTCCAACCTTCAAGCCACGGCCCAAGCAGAGCCCAAGGCCACTGA ACCCAAGCGCACCGCGACACCTCCAACCTTCA_GCCACGGCCCAAGCAGAGCCCAAGGCCACTGA CT C AL450998.2 Ensembl:ENSG00000179743 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:15835502..15835738 26863196 MeRIP-seq:(Medium) rs1341605217 Functional Loss DEL dbSNP153 33..33 33 - - - 63412 RMVar_ID_63412 Human_SNP_ID_4263067 m1A Human chr1 - 15835690 15835690 15835690 ACCCAAGCGCACCGCGACACCTCCAACCTTCAAGCCACGGCCCAAGCAGAGCCCAAGGCCACTGA ACCCAAGCGCACCGCGACACCTCCAACCTTCACGCCACGGCCCAAGCAGAGCCCAAGGCCACTGA T G AL450998.2 Ensembl:ENSG00000179743 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:15835502..15835738 26863196 MeRIP-seq:(Medium) rs1203140551 Functional Loss SNV dbSNP153 33..33 33 - - - 63413 RMVar_ID_63413 Human_SNP_ID_4263094 m1A Human chr1 - 15835735 15835735 15835735 GGGTGGGGAGCGCCAGGAAGCAAGCGTTTGAAAGAAAGCGAAAAAACCCAAGCGCACCGCGACAC GGGTGGGGAGCGCCAGGAAGCAAGCGTTTGAAGGAAAGCGAAAAAACCCAAGCGCACCGCGACAC T C AL450998.2 Ensembl:ENSG00000179743 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15835363..15835810 26863196 MeRIP-seq:(Medium) rs1330157175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334294 63414 RMVar_ID_63414 Human_SNP_ID_4263097 m1A Human chr1 - 15835746 15835746 15835746 GGGACGCTGGGGGGTGGGGAGCGCCAGGAAGCAAGCGTTTGAAAGAAAGCGAAAAAACCCAAGCG GGGACGCTGGGGGGTGGGGAGCGCCAGGAAGCCAGCGTTTGAAAGAAAGCGAAAAAACCCAAGCG T G AL450998.2 Ensembl:ENSG00000179743 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:15835475..15835827 26863196 MeRIP-seq:(Medium) rs1253164733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334294,Human_RBP_ID_4003212,Human_RBP_ID_8242042 63415 RMVar_ID_63415 Human_SNP_ID_4266892 m1A Human chr1 - 15847884 15847884 15847884 GTGCAGAGACCATCCCTCTCCCCCAGGTTCTGACTCTCGGGCCTCGCAGCTCAGCTCTGCCGCCA GTGCAGAGACCATCCCTCTCCCCCAGGTTCTGGCTCTCGGGCCTCGCAGCTCAGCTCTGCCGCCA T C AL450998.2 Ensembl:ENSG00000179743 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:15847801..15848188 26863196 MeRIP-seq:(Medium) rs963387164 Functional Loss SNV dbSNP153 33..33 33 - - - 63416 RMVar_ID_63416 Human_SNP_ID_4266912 m1A Human chr1 + 15847950 15847933 15847951 GGGGGGAGCCGGAGGAGCCGCCGCCGCTGCCGACGCCACCGCCGCAGCCGCCGCCGCCGCCGCCC GGGGGGAGCCGGAGGA__________________GCCACCGCCGCAGCCGCCGCCGCCGCCGCCC AGCCGCCGCCGCTGCCGAC A SPEN Ensembl:ENSG00000065526 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:15847901..15848076 26863196 MeRIP-seq:(Medium) rs1268493774 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_221090,Human_RBP_ID_741516,Human_RBP_ID_801067,Human_RBP_ID_4003348,Human_RBP_ID_5109003,Human_RBP_ID_5136089,Human_RBP_ID_5158613,Human_RBP_ID_5311541,Human_RBP_ID_5518441,Human_RBP_ID_8227730,Human_RBP_ID_8939942,Human_RBP_ID_9318620,Human_RBP_ID_9352359,Human_RBP_ID_9358112,Human_RBP_ID_18414867,Human_RBP_ID_18473693,Human_RBP_ID_22426029,Human_RBP_ID_22531912,Human_RBP_ID_26310263,Human_RBP_ID_26845066,Human_RBP_ID_27797395 RMVar_hsa_circ_96122,RMVar_hsa_circ_129481 63417 RMVar_ID_63417 Human_SNP_ID_4266917 m1A Human chr1 + 15847963 15847945 15847963 GGAGCCGCCGCCGCTGCCGACGCCACCGCCGCAGCCGCCGCCGCCGCCGCCCCGGCACCCGCCTC GGAGCCGCCGCCGCT__________________GCCGCCGCCGCCGCCGCCCCGGCACCCGCCTC TGCCGACGCCACCGCCGCA T SPEN Ensembl:ENSG00000065526 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:15847949..15848098 26863196 MeRIP-seq:(Medium) rs891226025 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_4003348,Human_RBP_ID_5109003,Human_RBP_ID_5136089,Human_RBP_ID_5158613,Human_RBP_ID_5311541,Human_RBP_ID_5518441,Human_RBP_ID_8939942,Human_RBP_ID_9318620,Human_RBP_ID_9352359,Human_RBP_ID_9358112,Human_RBP_ID_18414867,Human_RBP_ID_18473694,Human_RBP_ID_22426029,Human_RBP_ID_22532046,Human_RBP_ID_22562292,Human_RBP_ID_26310263,Human_RBP_ID_26845066,Human_RBP_ID_27797395 Human_miRNA_ID_2387704,Human_miRNA_ID_3029908 RMVar_hsa_circ_96122,RMVar_hsa_circ_129481 63418 RMVar_ID_63418 Human_SNP_ID_4266926 m1A Human chr1 + 15847963 15847963 15847963 GGAGCCGCCGCCGCTGCCGACGCCACCGCCGCAGCCGCCGCCGCCGCCGCCCCGGCACCCGCCTC GGAGCCGCCGCCGCTGCCGACGCCACCGCCGCCGCCGCCGCCGCCGCCGCCCCGGCACCCGCCTC A C SPEN Ensembl:ENSG00000065526 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:15847949..15848098 26863196 MeRIP-seq:(Medium) rs936341022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4003348,Human_RBP_ID_5109003,Human_RBP_ID_5136089,Human_RBP_ID_5158613,Human_RBP_ID_5311541,Human_RBP_ID_5518441,Human_RBP_ID_8939942,Human_RBP_ID_9318620,Human_RBP_ID_9352359,Human_RBP_ID_9358112,Human_RBP_ID_18414867,Human_RBP_ID_18473694,Human_RBP_ID_22426029,Human_RBP_ID_22532046,Human_RBP_ID_22562292,Human_RBP_ID_26310263,Human_RBP_ID_26845066,Human_RBP_ID_27797395 Human_miRNA_ID_2387704,Human_miRNA_ID_3029908 RMVar_hsa_circ_96122,RMVar_hsa_circ_129481 63419 RMVar_ID_63419 Human_SNP_ID_4267141 m1A Human chr1 - 15848611 15848610 15848612 CACCGCCTTTCCCTTCGCACGGAACCCTCCCGAAGTCAGACATTGCCGAGCGCCCGCAGAGCAGC CACCGCCTTTCCCTTCGCACGGAACCCTCCC__AGTCAGACATTGCCGAGCGCCCGCAGAGCAGC TTC T FLJ37453 RNACentral:URS00009AF023 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:15848507..15848628 32194978 MeRIP-seq:(Medium) rs1273419720 Functional Loss DEL dbSNP153 32..33 33 - - - 63420 RMVar_ID_63420 Human_SNP_ID_4267142 m1A Human chr1 - 15848611 15848611 15848611 CACCGCCTTTCCCTTCGCACGGAACCCTCCCGAAGTCAGACATTGCCGAGCGCCCGCAGAGCAGC CACCGCCTTTCCCTTCGCACGGAACCCTCCCGGAGTCAGACATTGCCGAGCGCCCGCAGAGCAGC T C FLJ37453 RNACentral:URS00009AF023 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:15848507..15848628 32194978 MeRIP-seq:(Medium) rs186151556 Functional Loss SNV dbSNP153 33..33 33 - - - 63421 RMVar_ID_63421 Human_SNP_ID_4270364 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC__________________________CTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..58 33 - - - 63422 RMVar_ID_63422 Human_SNP_ID_4270365 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC________________________ACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..56 33 - - - 63423 RMVar_ID_63423 Human_SNP_ID_4270366 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC______________________ACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..54 33 - - - 63424 RMVar_ID_63424 Human_SNP_ID_4270367 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC________________ACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..48 33 - - - 63425 RMVar_ID_63425 Human_SNP_ID_4270368 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC______________ACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..46 33 - - - 63426 RMVar_ID_63426 Human_SNP_ID_4270369 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC____________ACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..44 33 - - - 63427 RMVar_ID_63427 Human_SNP_ID_4270370 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC__________ACACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..42 33 - - - 63428 RMVar_ID_63428 Human_SNP_ID_4270371 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC________ACACACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..40 33 - - - 63429 RMVar_ID_63429 Human_SNP_ID_4270372 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC______ACACACACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..38 33 - - - 63430 RMVar_ID_63430 Human_SNP_ID_4270373 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC____ACACACACACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..36 33 - - - 63431 RMVar_ID_63431 Human_SNP_ID_4270374 m1A Human chr1 - 15860404 15860378 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACAC__ACACACACACACACACACACACACCTCTGAA GGTGTGTGTGTGTGTGTGTGTGTGTGT GGTGTGTGTGTGTGTGTGTGTGTGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs60005872 Functional Loss DEL dbSNP153 33..34 33 - - - 63432 RMVar_ID_63432 Human_SNP_ID_4270399 m1A Human chr1 - 15860404 15860404 15860404 GGGACCTTAGCTACACATACACACACACACACACACACACACACACACACACACACACCTCTGAA GGGACCTTAGCTACACATACACACACACACACTCACACACACACACACACACACACACCTCTGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15860400..15860478 26863196 MeRIP-seq:(Medium) rs1375517680 Functional Loss SNV dbSNP153 33..33 33 - - - 63433 RMVar_ID_63433 Human_SNP_ID_4289202 m1A Human chr1 + 15933242 15933242 15933242 ACTCTTGTTCGGAAAGACAAAGGGCGCCAGAAAACAACCCGATCACGCCGCAAGCGAAACACAAA ACTCTTGTTCGGAAAGACAAAGGGCGCCAGAAGACAACCCGATCACGCCGCAAGCGAAACACAAA A G SPEN Ensembl:ENSG00000065526 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:15933124..15933400;chr1:15933101..15933604;chr1:15933076..15933615;chr1:15933051..15933473 26863196 MeRIP-seq:(Medium) rs1192954183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17300,Human_RBP_ID_22130373,Human_RBP_ID_22706615 RMVar_hsa_circ_127083,RMVar_hsa_circ_129494 63434 RMVar_ID_63434 Human_SNP_ID_4289236 m1A Human chr1 + 15933319 15933319 15933319 GGCTCCTGTAGAGAGCCATGTCCCTGAATCCAACCAAGCTCAAGGTGAGAGTCCTGCTGCAAATG GGCTCCTGTAGAGAGCCATGTCCCTGAATCCAGCCAAGCTCAAGGTGAGAGTCCTGCTGCAAATG A G SPEN Ensembl:ENSG00000065526 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:15933163..15933348 26863196 MeRIP-seq:(Medium) rs780060759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17300,Human_RBP_ID_972298,Human_RBP_ID_1727939,Human_RBP_ID_8288662,Human_RBP_ID_8736906,Human_RBP_ID_17729016 RMVar_hsa_circ_127083,RMVar_hsa_circ_129494 63435 RMVar_ID_63435 Human_SNP_ID_4292175 m1A Human chr1 - 15942372 15942365 15942372 TGCAGTGACAGCCGATGAGACGGAAGTCCTGAAGGCCGAGATCAGCAAAGCTGTGAAGCAAGTGC TGCAGTGACAGCCGATGAGACGGAAGTCCTGA_______GATCAGCAAAGCTGTGAAGCAAGTGC CTCGGCCT C ZBTB17 Ensembl:ENSG00000116809 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:15941968..15942396 32194978 MeRIP-seq:(Medium) rs770238384 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_1105,Human_RBP_ID_18964724 Human_Splice_Rec_21425,Human_Splice_Rec_21430,Human_Splice_Rec_21431,Human_Splice_Rec_21460,Human_Splice_Rec_21461,Human_Splice_Rec_21488,Human_Splice_Rec_21489,Human_Splice_Rec_21518,Human_Splice_Rec_21519,Human_Splice_Rec_21530 RMVar_hsa_circ_13802 63436 RMVar_ID_63436 Human_SNP_ID_4292925 m1A Human chr1 - 15944406 15944406 15944406 GCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCCA GCACAGCGGCGAGAAGCCCTACCAGTGCGACTCCTGCGGCCGCTCCTTCTCCGACCCCACTTCCA T G ZBTB17 Ensembl:ENSG00000116809 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:15944355..15944437 26863196 MeRIP-seq:(Medium) rs1284187572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27390488 RMVar_hsa_circ_13802,RMVar_hsa_circ_57754,RMVar_hsa_circ_129502,RMVar_hsa_circ_21769,RMVar_hsa_circ_272315 63437 RMVar_ID_63437 Human_SNP_ID_4293213 m1A Human chr1 - 15945051 15945051 15945051 GAGGCCCCCGAGGAGAACGAGAATGAGGAGTCAGCGGGCACAGACTCGGGGCAGGAGCTCGGCTC GAGGCCCCCGAGGAGAACGAGAATGAGGAGTCTGCGGGCACAGACTCGGGGCAGGAGCTCGGCTC T A ZBTB17 Ensembl:ENSG00000116809 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:15945001..15945165 26863196 MeRIP-seq:(Medium) rs1413334410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853797,Human_RBP_ID_3935230,Human_RBP_ID_26313411 RMVar_hsa_circ_13802,RMVar_hsa_circ_57754,RMVar_hsa_circ_129502,RMVar_hsa_circ_272315 63438 RMVar_ID_63438 Human_SNP_ID_4294213 m1A Human chr1 + 15948487 15948487 15948487 AGCTGTTCCAAGACATGCTGGCTGTGCTGGGGAAAGTCCATGGCTGAAGAAAGCCAAAGGGCGTT AGCTGTTCCAAGACATGCTGGCTGTGCTGGGGTAAGTCCATGGCTGAAGAAAGCCAAAGGGCGTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15948260..15948499 26863196 MeRIP-seq:(Medium) rs759119828 Functional Loss SNV dbSNP153 33..33 33 - - - 63439 RMVar_ID_63439 Human_SNP_ID_4296237 m1A Human chr1 - 15957240 15957240 15957240 CTCCCTCTTAAACCTCATTCAGGTCTTTGCTTAAATGCCACCTCCTCTGAGGTCCCCCTTGCCTC CTCCCTCTTAAACCTCATTCAGGTCTTTGCTTGAATGCCACCTCCTCTGAGGTCCCCCTTGCCTC T C ZBTB17 Ensembl:ENSG00000116809 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:15957227..15957354 26863196 MeRIP-seq:(Medium) rs1160472185 Functional Loss SNV dbSNP153 33..33 33 - - - 63440 RMVar_ID_63440 Human_SNP_ID_4310518 m1A Human chr1 + 16015000 16015000 16015000 CTCTGCCCTGGCACAGCCAGCTGGCTGGGGGCACGGGGTGGGCAGGCAGCCTGCTCGCTGGCGTG CTCTGCCCTGGCACAGCCAGCTGGCTGGGGGCGCGGGGTGGGCAGGCAGCCTGCTCGCTGGCGTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:16014951..16015000 26863196 MeRIP-seq:(Medium) rs867352564 Functional Loss SNV dbSNP153 33..33 33 - - - 63441 RMVar_ID_63441 Human_SNP_ID_4310664 m1A Human chr1 + 16015574 16015574 16015574 GTGGGGCGGGGGGACAGGGAAAGGGAAGGGAGAGGCACTCAGATTTTGATCTCCGTCCGGAAGGT GTGGGGCGGGGGGACAGGGAAAGGGAAGGGAGGGGCACTCAGATTTTGATCTCCGTCCGGAAGGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:16015526..16015575 26863196 MeRIP-seq:(Medium) rs766622342 Functional Loss SNV dbSNP153 33..33 33 - - - 63442 RMVar_ID_63442 Human_SNP_ID_4311471 m1A Human chr1 - 16017888 16017888 16017888 TCCATTCCTCTTCCTCTTCCTCCTCCTCTTCCACCTCCTCCTCGGCCTCCCGTGCTCTCCCGGCC TCCATTCCTCTTCCTCTTCCTCCTCCTCTTCCCCCTCCTCCTCGGCCTCCCGTGCTCTCCCGGCC T G HSPB7 Ensembl:ENSG00000173641 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:16017837..16018025 26863196 MeRIP-seq:(Medium) rs779032380 Functional Loss SNV dbSNP153 33..33 33 - - - 63443 RMVar_ID_63443 Human_SNP_ID_4311525 m1A Human chr1 + 16017998 16017998 16017998 ACGGACGGCGCCGGGCCCTGCCCAGGCGGGCGAGGGCTGGACAGGAGAGGGTGTGGGCGCAGGCC ACGGACGGCGCCGGGCCCTGCCCAGGCGGGCGGGGGCTGGACAGGAGAGGGTGTGGGCGCAGGCC A G lnc-SRARP-2 RNACentral:URS00008C1639 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:16017976..16018000 26863196 MeRIP-seq:(Medium) rs772523460 Functional Loss SNV dbSNP153 33..33 33 - - - 63444 RMVar_ID_63444 Human_SNP_ID_4321829 m1A Human chr1 + 16049055 16049055 16049055 GACAGATGGGTCAGGGAGGAGGTGACATGGGGAGGGGGTCCTACAGTCACAGGTGGGTGGGGGTG GACAGATGGGTCAGGGAGGAGGTGACATGGGGTGGGGGTCCTACAGTCACAGGTGGGTGGGGGTG A T CLCNKB Ensembl:ENSG00000184908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16048836..16049165 26863196 MeRIP-seq:(Medium) rs1174871901 Functional Loss SNV dbSNP153 33..33 33 - - - 63445 RMVar_ID_63445 Human_SNP_ID_4322303 m1A Human chr1 + 16050088 16050088 16050088 CACCACCTACAAGTCCCCACAGTCACTGCCCGACTACCTTACTGGCCTCAAACCTCCCCATTTAA CACCACCTACAAGTCCCCACAGTCACTGCCCGCCTACCTTACTGGCCTCAAACCTCCCCATTTAA A C CLCNKB Ensembl:ENSG00000184908 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:16049998..16050125 26863196 MeRIP-seq:(Medium) rs1178973855 Functional Loss SNV dbSNP153 33..33 33 - - - 63446 RMVar_ID_63446 Human_SNP_ID_4327445 m1A Human chr1 - 16064908 16064908 16064908 GAGGCCAGAGGCCAGGATAAGAGCGAGGCTCAAGAGGGCAGGAAGGCTGCACAGCTCCAGCTCCA GAGGCCAGAGGCCAGGATAAGAGCGAGGCTCAGGAGGGCAGGAAGGCTGCACAGCTCCAGCTCCA T C FAM131C Ensembl:ENSG00000185519 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16064906..16064989 26863196 MeRIP-seq:(Medium) rs1191414990 Functional Loss SNV dbSNP153 33..33 33 - - - 63447 RMVar_ID_63447 Human_SNP_ID_4329494 m1A Human chr1 - 16073482 16073445 16073482 GGCCCGCGGAGACATGAACGCCCCGCGGCCCCACGCACCCCGGGCGCAGCGGCCCGGCCCCGCGG GGCCCGCGGAGACATGAACGCCCCGCGGCCCC_________________________________ CGGGGCCGCGGGGCCGGGCCGCTGCGCCCGGGGTGCGT C FAM131C Ensembl:ENSG00000185519 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16062521..16073632 26863196 MeRIP-seq:(Medium) rs1460987133 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_4004688 Human_Splice_Rec_21899,Human_Splice_Rec_21911 63448 RMVar_ID_63448 Human_SNP_ID_4344788 m1A Human chr1 + 16130338 16130338 16130338 CTTGGGGCGGCGGGCACGCTCCTGCTGCCAGCACTGCATCATGAGCTGGTAGATGGCGGAGGGGC CTTGGGGCGGCGGGCACGCTCCTGCTGCCAGCGCTGCATCATGAGCTGGTAGATGGCGGAGGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16130287..16130444 26863196 MeRIP-seq:(Medium) rs1437259118 Functional Loss SNV dbSNP153 33..33 33 - - - 63449 RMVar_ID_63449 Human_SNP_ID_4345827 m1A Human chr1 - 16133602 16133602 16133602 CCTGTGACCCCACCCCTTCTCCTTCCAGAACAACTGAAGCCCCTGAAGACATACGTGGACCCCCA CCTGTGACCCCACCCCTTCTCCTTCCAGAACAGCTGAAGCCCCTGAAGACATACGTGGACCCCCA T C EPHA2 Ensembl:ENSG00000142627 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16133501..16133625 32194978 MeRIP-seq:(Medium) rs773033022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21938 RMVar_hsa_circ_17911,RMVar_hsa_circ_90144,RMVar_hsa_circ_9730,RMVar_hsa_circ_113533,RMVar_hsa_circ_129505,RMVar_hsa_circ_101041,RMVar_hsa_circ_129507,RMVar_hsa_circ_85372,RMVar_hsa_circ_129508,RMVar_hsa_circ_129506,RMVar_hsa_circ_89795,RMVar_hsa_circ_92235,RMVar_hsa_circ_121987,RMVar_hsa_circ_129509,RMVar_hsa_circ_129510,RMVar_hsa_circ_129512,RMVar_hsa_circ_80232,RMVar_hsa_circ_129511 63450 RMVar_ID_63450 Human_SNP_ID_4346557 m1A Human chr1 - 16135749 16135749 16135749 GTCCTGCCCAGAGCCCCCCAAGGTGAGGCTGGAGGGCCGCAGCACCACCTCGCTTAGCGTCTCCT GTCCTGCCCAGAGCCCCCCAAGGTGAGGCTGGTGGGCCGCAGCACCACCTCGCTTAGCGTCTCCT T A EPHA2 Ensembl:ENSG00000142627 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16135701..16135750 32194978 MeRIP-seq:(Medium) rs144075562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21930,Human_Splice_Rec_21931,Human_Splice_Rec_21960,Human_Splice_Rec_21961 Human_miRNA_ID_2972003 RMVar_hsa_circ_17911,RMVar_hsa_circ_9730,RMVar_hsa_circ_113533,RMVar_hsa_circ_129505,RMVar_hsa_circ_101041,RMVar_hsa_circ_129508,RMVar_hsa_circ_89795,RMVar_hsa_circ_92235,RMVar_hsa_circ_129510,RMVar_hsa_circ_129512,RMVar_hsa_circ_332131 63451 RMVar_ID_63451 Human_SNP_ID_4346558 m1A Human chr1 - 16135749 16135749 16135749 GTCCTGCCCAGAGCCCCCCAAGGTGAGGCTGGAGGGCCGCAGCACCACCTCGCTTAGCGTCTCCT GTCCTGCCCAGAGCCCCCCAAGGTGAGGCTGGGGGGCCGCAGCACCACCTCGCTTAGCGTCTCCT T C EPHA2 Ensembl:ENSG00000142627 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16135701..16135750 32194978 MeRIP-seq:(Medium) rs144075562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21930,Human_Splice_Rec_21931,Human_Splice_Rec_21960,Human_Splice_Rec_21961 Human_miRNA_ID_2972003 RMVar_hsa_circ_17911,RMVar_hsa_circ_9730,RMVar_hsa_circ_113533,RMVar_hsa_circ_129505,RMVar_hsa_circ_101041,RMVar_hsa_circ_129508,RMVar_hsa_circ_89795,RMVar_hsa_circ_92235,RMVar_hsa_circ_129510,RMVar_hsa_circ_129512,RMVar_hsa_circ_332131 63452 RMVar_ID_63452 Human_SNP_ID_4347629 m1A Human chr1 + 16138413 16138413 16138413 CAAGCAGGGGCTCTCAGATGCCTCAAACTTAAAAAATCCAGGCGAGCAGGCTGGTGGACACAGGA CAAGCAGGGGCTCTCAGATGCCTCAAACTTAAGAAATCCAGGCGAGCAGGCTGGTGGACACAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16138276..16138450 32194978 MeRIP-seq:(Medium) rs770990201 Functional Loss SNV dbSNP153 33..33 33 - - - 63453 RMVar_ID_63453 Human_SNP_ID_4348919 m1A Human chr1 - 16143419 16143419 16143419 CTCCACAGGTGTGCCACAGGTGTGCCAAAGTTAGGCTCTTGTGTAAGGCAGGTAGGCATCCTGGT CTCCACAGGTGTGCCACAGGTGTGCCAAAGTTGGGCTCTTGTGTAAGGCAGGTAGGCATCCTGGT T C EPHA2 Ensembl:ENSG00000142627 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16143417..16143702 26863196 MeRIP-seq:(Medium) rs1001772839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17911,RMVar_hsa_circ_101041,RMVar_hsa_circ_129508,RMVar_hsa_circ_89795,RMVar_hsa_circ_92235,RMVar_hsa_circ_129510,RMVar_hsa_circ_129512,RMVar_hsa_circ_95433,RMVar_hsa_circ_129516 63454 RMVar_ID_63454 Human_SNP_ID_4350444 m1A Human chr1 + 16149047 16149047 16149047 CATGTCATTCATGATGTTCTGCATCAGGTCCCACTGTGGGGGGAAGATACAGGTTAGTGTGGGCA CATGTCATTCATGATGTTCTGCATCAGGTCCCGCTGTGGGGGGAAGATACAGGTTAGTGTGGGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16148783..16149080 26863196 MeRIP-seq:(Medium) rs1491004267 Functional Loss SNV dbSNP153 33..33 33 - - - 63455 RMVar_ID_63455 Human_SNP_ID_4352253 m1A Human chr1 + 16155880 16155880 16155880 CTTCCTTGCCCTGCGCCGCCGCGGCCGCGGCCAGCGCACAGCCCCACAGCAGGGCGAAGCAGGCG CTTCCTTGCCCTGCGCCGCCGCGGCCGCGGCCGGCGCACAGCCCCACAGCAGGGCGAAGCAGGCG A G AL451042.2 Ensembl:ENSG00000227959 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16155851..16155950 32194978 MeRIP-seq:(Medium) rs1253449807 Functional Loss SNV dbSNP153 33..33 33 - - - 63456 RMVar_ID_63456 Human_SNP_ID_4352300 m1A Human chr1 - 16156009 16156009 16156009 AGTTGCGCGCAGGCCGGCGGGCGGGAGCGGACACCGAGGCCGGCGTGCAGGCGTGCGGGTGTGCG AGTTGCGCGCAGGCCGGCGGGCGGGAGCGGACCCCGAGGCCGGCGTGCAGGCGTGCGGGTGTGCG T G EPHA2 Ensembl:ENSG00000142627 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16148966..16156075 26863196 MeRIP-seq:(Medium) rs1289052272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20629,Human_RBP_ID_4072566,Human_RBP_ID_18414868,Human_RBP_ID_22428123 RMVar_hsa_circ_95433,RMVar_hsa_circ_129516 63457 RMVar_ID_63457 Human_SNP_ID_4363769 m1A Human chr1 + 16198302 16198302 16198302 ACCAAGAGTCAGGCAGGATTGAGGACATAGAAAGGAGAGGGCCCCAGTCTTTGCCAGGTATCAGT ACCAAGAGTCAGGCAGGATTGAGGACATAGAAGGGAGAGGGCCCCAGTCTTTGCCAGGTATCAGT A G ARHGEF19-AS1 Ensembl:ENSG00000234166 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:16198252..16198353 32194978 MeRIP-seq:(Medium) rs907722886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21970 63458 RMVar_ID_63458 Human_SNP_ID_4365906 m1A Human chr1 - 16206231 16206231 16206231 TGCCGAGCTGAGCGAGTGTCTGGGGGCGCAGGACAAGCAGTGGCTGTTTTCCAAACTGCCCGAGG TGCCGAGCTGAGCGAGTGTCTGGGGGCGCAGGGCAAGCAGTGGCTGTTTTCCAAACTGCCCGAGG T C ARHGEF19 Ensembl:ENSG00000142632 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16205923..16206369 32194978 MeRIP-seq:(Medium) rs1299504529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073592 Human_Splice_Rec_21973,Human_Splice_Rec_22003,Human_Splice_Rec_22021,Human_Splice_Rec_22031,Human_Splice_Rec_22041,Human_Splice_Rec_22043 RMVar_hsa_circ_94790,RMVar_hsa_circ_98742,RMVar_hsa_circ_90184,RMVar_hsa_circ_129523,RMVar_hsa_circ_129524,RMVar_hsa_circ_129525,RMVar_hsa_circ_129526,RMVar_hsa_circ_97587 63459 RMVar_ID_63459 Human_SNP_ID_4366276 m1A Human chr1 - 16206995 16206995 16206995 CGCTGTGGCAGGATATCCCCGACGTACGCGGCAGCGGCGTCCTGGCCACGCTGAGCCTGCGGGAC CGCTGTGGCAGGATATCCCCGACGTACGCGGCCGCGGCGTCCTGGCCACGCTGAGCCTGCGGGAC T G ARHGEF19 Ensembl:ENSG00000142632 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:16206871..16206997 26863196 MeRIP-seq:(Medium) rs1376475417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_21971,Human_Splice_Rec_22001,Human_Splice_Rec_22039 RMVar_hsa_circ_94790,RMVar_hsa_circ_98742,RMVar_hsa_circ_90184,RMVar_hsa_circ_129523,RMVar_hsa_circ_129524,RMVar_hsa_circ_129525,RMVar_hsa_circ_129526,RMVar_hsa_circ_97587 63460 RMVar_ID_63460 Human_SNP_ID_4369310 m1A Human chr1 + 16217329 16217329 16217329 GAATCTGGCCCTGCCCGTTCAGCCAGTACCCTAGCCGGCTCCGCGCATTTGTCCGGGGCAGAATC GAATCTGGCCCTGCCCGTTCAGCCAGTACCCTGGCCGGCTCCGCGCATTTGTCCGGGGCAGAATC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:16217279..16217408 26863196 MeRIP-seq:(Medium) rs1008955026 Functional Loss SNV dbSNP153 33..33 33 - - - 63461 RMVar_ID_63461 Human_SNP_ID_4386465 m1A Human chr1 - 16287051 16287051 16287051 CTGTTGTAAGGACATTGTCATATTCACTGAATAGAATGGCTAGTTGTGTAGGTTTCTGAGAAGAG CTGTTGTAAGGACATTGTCATATTCACTGAATTGAATGGCTAGTTGTGTAGGTTTCTGAGAAGAG T A FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16287048..16287284 26863196 MeRIP-seq:(Medium) rs1557585284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9464189,Human_RBP_ID_10635665 RMVar_hsa_circ_54825,RMVar_hsa_circ_337018,RMVar_hsa_circ_129532 63462 RMVar_ID_63462 Human_SNP_ID_4403892 m1A Human chr1 + 16352406 16352406 16352406 CCTCACAGCTGGCGGGACCCCGAGCCGCCCGGAGCCGCCATCTTCCTCCACTCAAACGCCGCCGC CCTCACAGCTGGCGGGACCCCGAGCCGCCCGGGGCCGCCATCTTCCTCCACTCAAACGCCGCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:16315285..16352450;chr1:16315335..16352450;chr1:16352275..16352450 26863196 MeRIP-seq:(Medium) rs1435279385 Functional Loss SNV dbSNP153 33..33 33 - - - 63463 RMVar_ID_63463 Human_SNP_ID_4408127 m1A Human chr1 - 16367278 16367278 16367278 ACCCCGCTGTCTGCCGCCTCTTCCCAGCTCTCAGCGACCTCCTCATCTTCCATCTTACTCGCCGC ACCCCGCTGTCTGCCGCCTCTTCCCAGCTCTCGGCGACCTCCTCATCTTCCATCTTACTCGCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16367226..16367406 26863196 MeRIP-seq:(Medium) rs1391189066 Functional Loss SNV dbSNP153 33..33 33 - - - 63464 RMVar_ID_63464 Human_SNP_ID_4409699 m1A Human chr1 + 16372934 16372934 16372934 GGGTACCATGGCTGGATCAGAGAAAGTCTTGTAAAGAAGACGATGCCTAAGTTAAGATTTGAAAG GGGTACCATGGCTGGATCAGAGAAAGTCTTGTGAAGAAGACGATGCCTAAGTTAAGATTTGAAAG A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16372931..16373008 26863196 MeRIP-seq:(Medium) rs181533531 Functional Loss SNV dbSNP153 33..33 33 - - - 63465 RMVar_ID_63465 Human_SNP_ID_4415054 m1A Human chr1 + 16393272 16393272 16393272 ATCTCCTCCCAAAGTGCCCATTGTGATTCAGGACGATAGCCTTCCCGCGGGGCCCCCTCCACAGA ATCTCCTCCCAAAGTGCCCATTGTGATTCAGGGCGATAGCCTTCCCGCGGGGCCCCCTCCACAGA A G SZRD1 Ensembl:ENSG00000055070 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16391351..16393426 26863196 MeRIP-seq:(Medium) rs1212506179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331541,Human_RBP_ID_1414892,Human_RBP_ID_3285328,Human_RBP_ID_4084329,Human_RBP_ID_5707000,Human_RBP_ID_8289345,Human_RBP_ID_10637738,Human_RBP_ID_18186861,Human_RBP_ID_18555250,Human_RBP_ID_22486316,Human_RBP_ID_26310315,Human_RBP_ID_26846098,Human_RBP_ID_27171112 Human_Splice_Rec_22112,Human_Splice_Rec_22116,Human_Splice_Rec_22120,Human_Splice_Rec_22128,Human_Splice_Rec_22134,Human_Splice_Rec_22142,Human_Splice_Rec_22148,Human_Splice_Rec_22156,Human_Splice_Rec_22160,Human_Splice_Rec_22166 RMVar_hsa_circ_46115,RMVar_hsa_circ_24913 63466 RMVar_ID_63466 Human_SNP_ID_4415486 m1A Human chr1 - 16395028 16395028 16395028 CGGGTTGGGAGATCCTGGTTGGCCTGAAAGGAAGAAAAGCAGAGGAAGGCCTGAAGAAGGATATA CGGGTTGGGAGATCCTGGTTGGCCTGAAAGGATGAAAAGCAGAGGAAGGCCTGAAGAAGGATATA T A SPATA21 Ensembl:ENSG00000187144 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16395026..16395050 26863196 MeRIP-seq:(Medium) rs201628336 Functional Loss SNV dbSNP153 33..33 33 - - - 63467 RMVar_ID_63467 Human_SNP_ID_4415487 m1A Human chr1 - 16395028 16395028 16395028 CGGGTTGGGAGATCCTGGTTGGCCTGAAAGGAAGAAAAGCAGAGGAAGGCCTGAAGAAGGATATA CGGGTTGGGAGATCCTGGTTGGCCTGAAAGGAGGAAAAGCAGAGGAAGGCCTGAAGAAGGATATA T C SPATA21 Ensembl:ENSG00000187144 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16395026..16395050 26863196 MeRIP-seq:(Medium) rs201628336 Functional Loss SNV dbSNP153 33..33 33 - - - 63468 RMVar_ID_63468 Human_SNP_ID_4416010 m1A Human chr1 - 16397195 16397195 16397195 ACCAGTCCCTGCCACATCCTCAATCCACAGACACCCACCAGCCAGCCTTTACTTTGGCCTCCCAC ACCAGTCCCTGCCACATCCTCAATCCACAGACCCCCACCAGCCAGCCTTTACTTTGGCCTCCCAC T G SPATA21 Ensembl:ENSG00000187144 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16397145..16397396 32194978 MeRIP-seq:(Medium) rs1010604885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100409,RMVar_hsa_circ_129540 63469 RMVar_ID_63469 Human_SNP_ID_4427695 m1A Human chr1 + 16440817 16440817 16440817 GGTGCTCTGTGTCAAGCCTGACGTCCACGTCTACCGCATCCCTCCGCGGGCTACCAACCGTGGCT GGTGCTCTGTGTCAAGCCTGACGTCCACGTCTGCCGCATCCCTCCGCGGGCTACCAACCGTGGCT A G NECAP2 Ensembl:ENSG00000157191 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16440770..16441232 32194978 MeRIP-seq:(Medium) rs770224883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4006228,Human_RBP_ID_5311547,Human_RBP_ID_19034007,Human_RBP_ID_22426918,Human_RBP_ID_26313416 Human_Splice_Rec_22267,Human_Splice_Rec_22291,Human_Splice_Rec_22305,Human_Splice_Rec_22307,Human_Splice_Rec_22319,Human_Splice_Rec_22329,Human_Splice_Rec_22337,Human_Splice_Rec_22353,Human_Splice_Rec_22369,Human_Splice_Rec_22381 63470 RMVar_ID_63470 Human_SNP_ID_4429545 m1A Human chr1 - 16447976 16447976 16447976 CCCAAGAGGAGGAAGCACCAGGACCCATGCCTACCATTTCCATCTTCGATGCGGATCACGAAGTA CCCAAGAGGAGGAAGCACCAGGACCCATGCCTCCCATTTCCATCTTCGATGCGGATCACGAAGTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr1:16447940..16448033;chr1:16447926..16448111 26863196,32194978 MeRIP-seq:(Medium) rs112683579 Functional Loss SNV dbSNP153 33..33 33 - - - 63471 RMVar_ID_63471 Human_SNP_ID_4432724 m1A Human chr1 + 16459579 16459579 16459579 ATTCCTCACTGTGGGCAGCTGCCCTGAGCTTCAGGCAGCAGTGTTTATCTCTGGCCAGTTGTCTG ATTCCTCACTGTGGGCAGCTGCCCTGAGCTTCGGGCAGCAGTGTTTATCTCTGGCCAGTTGTCTG A G NECAP2 Ensembl:ENSG00000157191 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16459531..16459681 32194978 MeRIP-seq:(Medium) rs906944820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224271,Human_RBP_ID_1728527,Human_RBP_ID_2102511,Human_RBP_ID_17223720,Human_RBP_ID_26385367 63472 RMVar_ID_63472 Human_SNP_ID_4433946 m1A Human chr1 + 16464124 16464123 16464125 TGAGAAATGCAGAGAAATTATATAATTTGTTCAAAGTCACATGGTTGGTAAGTGGCAGAGCTGGG TGAGAAATGCAGAGAAATTATATAATTTGTTC__AGTCACATGGTTGGTAAGTGGCAGAGCTGGG CAA C LINC01772 Ensembl:ENSG00000226029 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16464029..16464139 26863410 MeRIP-seq:(Medium) rs1212468824 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5708692 63473 RMVar_ID_63473 Human_SNP_ID_4433947 m1A Human chr1 + 16464124 16464124 16464124 TGAGAAATGCAGAGAAATTATATAATTTGTTCAAAGTCACATGGTTGGTAAGTGGCAGAGCTGGG TGAGAAATGCAGAGAAATTATATAATTTGTTCGAAGTCACATGGTTGGTAAGTGGCAGAGCTGGG A G LINC01772 Ensembl:ENSG00000226029 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16464029..16464139 26863410 MeRIP-seq:(Medium) rs559094472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5708692 63474 RMVar_ID_63474 Human_SNP_ID_4433948 m1A Human chr1 + 16464124 16464124 16464124 TGAGAAATGCAGAGAAATTATATAATTTGTTCAAAGTCACATGGTTGGTAAGTGGCAGAGCTGGG TGAGAAATGCAGAGAAATTATATAATTTGTTCTAAGTCACATGGTTGGTAAGTGGCAGAGCTGGG A T LINC01772 Ensembl:ENSG00000226029 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16464029..16464139 26863410 MeRIP-seq:(Medium) rs559094472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5708692 63475 RMVar_ID_63475 Human_SNP_ID_4437442 m1A Human chr1 - 16477057 16477057 16477057 CCCTCTGTCCTGCAGCCATAGACAACTGGAGCAGCTGGAAGGGAAGCGCTCAGTCCTGGCCAAGG CCCTCTGTCCTGCAGCCATAGACAACTGGAGCGGCTGGAAGGGAAGCGCTCAGTCCTGGCCAAGG T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16477026..16477126 32194978 MeRIP-seq:(Medium) rs1163638010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22416,Human_Splice_Rec_22438,Human_Splice_Rec_22464 RMVar_hsa_circ_37043,RMVar_hsa_circ_309385,RMVar_hsa_circ_278673,RMVar_hsa_circ_35504,RMVar_hsa_circ_22811,RMVar_hsa_circ_338142 63476 RMVar_ID_63476 Human_SNP_ID_4441305 m1A Human chr1 - 16490601 16490601 16490601 GAGGCGCGAGGAGGAGGTGGGCATGGGGGTGCAGGGAGGCCAGCCTGACCCAAGGGGAGGGGCAC GAGGCGCGAGGAGGAGGTGGGCATGGGGGTGCGGGGAGGCCAGCCTGACCCAAGGGGAGGGGCAC T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16490593..16490893 26863196 MeRIP-seq:(Medium) rs370975219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9412759 RMVar_hsa_circ_29093,RMVar_hsa_circ_37043,RMVar_hsa_circ_278673,RMVar_hsa_circ_35504,RMVar_hsa_circ_59751,RMVar_hsa_circ_129546,RMVar_hsa_circ_79050,RMVar_hsa_circ_101813,RMVar_hsa_circ_129547 63477 RMVar_ID_63477 Human_SNP_ID_4441347 m1A Human chr1 + 16490705 16490705 16490705 GTCCAGTCATTGGTCACCTTTTGTATGTCCTCACTCAGAGCCTGGTTGGCCGAGCCTGCCTGGTC GTCCAGTCATTGGTCACCTTTTGTATGTCCTCGCTCAGAGCCTGGTTGGCCGAGCCTGCCTGGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16490609..16490724 26863196 MeRIP-seq:(Medium) rs957123795 Functional Loss SNV dbSNP153 33..33 33 - - - 63478 RMVar_ID_63478 Human_SNP_ID_4443475 m1A Human chr1 - 16499063 16499063 16499063 CGCTGTGGGCGCCGCGCCCGCCGCTGCCCGGCACCGGAAGCCAAGAGGGCGTTCCCGACGGGCTC CGCTGTGGGCGCCGCGCCCGCCGCTGCCCGGCGCCGGAAGCCAAGAGGGCGTTCCCGACGGGCTC T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16499059..16499206 26863196 MeRIP-seq:(Medium) rs1484682321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18414869 63479 RMVar_ID_63479 Human_SNP_ID_4443492 m1A Human chr1 - 16499100 16499100 16499100 CTGGGGGCGGGCTGGAGCCATGTCCCGGGGCTAGGGGCGCTGTGGGCGCCGCGCCCGCCGCTGCC CTGGGGGCGGGCTGGAGCCATGTCCCGGGGCTGGGGGCGCTGTGGGCGCCGCGCCCGCCGCTGCC T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:16499098..16499234;chr1:16499097..16499243 26863196 MeRIP-seq:(Medium) rs985003089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334011,Human_RBP_ID_5160791,Human_RBP_ID_5334805,Human_RBP_ID_8171248,Human_RBP_ID_8724984,Human_RBP_ID_18414869,Human_RBP_ID_19443175 63480 RMVar_ID_63480 Human_SNP_ID_4457567 m1A Human chr1 - 16535294 16535294 16535294 TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAATTGTTTTACACTGGCCG TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGGTTCCCGGTCAGGGAATTGTTTTACACTGGCCG T C LINC01783 Ensembl:ENSG00000233421 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1256726644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223365,Human_RBP_ID_746607,Human_RBP_ID_1439086,Human_RBP_ID_3333755,Human_RBP_ID_4077251,Human_RBP_ID_5086445,Human_RBP_ID_5161177,Human_RBP_ID_5272938,Human_RBP_ID_5433174,Human_RBP_ID_5484825,Human_RBP_ID_5891687,Human_RBP_ID_8171367,Human_RBP_ID_8240297,Human_RBP_ID_8289875,Human_RBP_ID_8755924,Human_RBP_ID_8958080,Human_RBP_ID_9340552,Human_RBP_ID_9553409,Human_RBP_ID_19045064,Human_RBP_ID_19443375,Human_RBP_ID_22531361,Human_RBP_ID_23121723,Human_RBP_ID_23343512,Human_RBP_ID_24529087,Human_RBP_ID_26753274,Human_RBP_ID_26872615 Human_miRNA_ID_3208935 63481 RMVar_ID_63481 Human_SNP_ID_4457568 m1A Human chr1 - 16535294 16535294 16535294 TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAATTGTTTTACACTGGCCG TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGCTTCCCGGTCAGGGAATTGTTTTACACTGGCCG T G LINC01783 Ensembl:ENSG00000233421 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1256726644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223365,Human_RBP_ID_746607,Human_RBP_ID_1439086,Human_RBP_ID_3333755,Human_RBP_ID_4077251,Human_RBP_ID_5086445,Human_RBP_ID_5161177,Human_RBP_ID_5272938,Human_RBP_ID_5433174,Human_RBP_ID_5484825,Human_RBP_ID_5891687,Human_RBP_ID_8171367,Human_RBP_ID_8240297,Human_RBP_ID_8289875,Human_RBP_ID_8755924,Human_RBP_ID_8958080,Human_RBP_ID_9340552,Human_RBP_ID_9553409,Human_RBP_ID_19045064,Human_RBP_ID_19443375,Human_RBP_ID_22531361,Human_RBP_ID_23121723,Human_RBP_ID_23343512,Human_RBP_ID_24529087,Human_RBP_ID_26753274,Human_RBP_ID_26872615 Human_miRNA_ID_3208935 63482 RMVar_ID_63482 Human_SNP_ID_4462538 m1A Human chr1 - 16545936 16545936 16545936 GAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTTATC GAGACCCGGGTTCAATTCCCGGCCAATGCAAGGGGGTCTTTTTCACCCCGCTGTTGCTCTTTATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16545909..16545991 26863196 MeRIP-seq:(Medium) rs1160286193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1150474,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5413204,Human_RBP_ID_5484826,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171395 63483 RMVar_ID_63483 Human_SNP_ID_4462539 m1A Human chr1 - 16545936 16545936 16545936 GAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTTATC GAGACCCGGGTTCAATTCCCGGCCAATGCAAGCGGGTCTTTTTCACCCCGCTGTTGCTCTTTATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16545909..16545991 26863196 MeRIP-seq:(Medium) rs1160286193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1150474,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5413204,Human_RBP_ID_5484826,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171395 63484 RMVar_ID_63484 Human_SNP_ID_4462544 m1A Human chr1 - 16545939 16545939 16545939 CGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT CGGGAGACCCGGGTTCAATTCCCGGCCAATGCTAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT T A tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:16545871..16545992 26863196 MeRIP-seq:(Medium) rs1423680006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63485 RMVar_ID_63485 Human_SNP_ID_4462545 m1A Human chr1 - 16545939 16545939 16545939 CGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT CGGGAGACCCGGGTTCAATTCCCGGCCAATGCGAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:16545871..16545992 26863196 MeRIP-seq:(Medium) rs1423680006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63486 RMVar_ID_63486 Human_SNP_ID_4462546 m1A Human chr1 - 16545939 16545939 16545939 CGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT CGGGAGACCCGGGTTCAATTCCCGGCCAATGCCAGAGGGTCTTTTTCACCCCGCTGTTGCTCTTT T G tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:16545871..16545992 26863196 MeRIP-seq:(Medium) rs1423680006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63487 RMVar_ID_63487 Human_SNP_ID_4462555 m1A Human chr1 - 16545943 16545943 16545943 CACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT CACGCGGGAGACCCGGGTTCAATTCCCGGCCAGTGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16545899..16546003 26863196 MeRIP-seq:(Medium) rs188712584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_21999636,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63488 RMVar_ID_63488 Human_SNP_ID_4462556 m1A Human chr1 - 16545943 16545943 16545943 CACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT CACGCGGGAGACCCGGGTTCAATTCCCGGCCACTGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT T G tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16545899..16546003 26863196 MeRIP-seq:(Medium) rs188712584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_21999636,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63489 RMVar_ID_63489 Human_SNP_ID_4462557 m1A Human chr1 - 16545944 16545944 16545944 CCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC CCACGCGGGAGACCCGGGTTCAATTCCCGGCCTATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC T A tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:16545916..16546001 26863410 MeRIP-seq:(Medium) rs141853250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63490 RMVar_ID_63490 Human_SNP_ID_4462558 m1A Human chr1 - 16545944 16545944 16545944 CCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC CCACGCGGGAGACCCGGGTTCAATTCCCGGCCGATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:16545916..16546001 26863410 MeRIP-seq:(Medium) rs141853250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63491 RMVar_ID_63491 Human_SNP_ID_4462559 m1A Human chr1 - 16545944 16545944 16545944 CCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC CCACGCGGGAGACCCGGGTTCAATTCCCGGCCCATGCAAGAGGGTCTTTTTCACCCCGCTGTTGC T G tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:16545916..16546001 26863410 MeRIP-seq:(Medium) rs141853250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 63492 RMVar_ID_63492 Human_SNP_ID_4462576 m1A Human chr1 - 16545954 16545954 16545954 TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACC TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAGTTCCCGGCCAATGCAAGAGGGTCTTTTTCACC T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1323440553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1415120,Human_RBP_ID_5252964,Human_RBP_ID_5273285,Human_RBP_ID_5710284,Human_RBP_ID_8289878,Human_RBP_ID_9556181,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555622,Human_RBP_ID_19446039,Human_RBP_ID_21999637,Human_RBP_ID_22130936,Human_RBP_ID_22786834,Human_RBP_ID_22849847,Human_RBP_ID_23112693,Human_RBP_ID_23121725,Human_RBP_ID_23343520,Human_RBP_ID_26846452,Human_RBP_ID_27390926,Human_RBP_ID_27554640 63493 RMVar_ID_63493 Human_SNP_ID_4462577 m1A Human chr1 - 16545954 16545954 16545954 TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACC TTCTCGCCTCCCACGCGGGAGACCCGGGTTCACTTCCCGGCCAATGCAAGAGGGTCTTTTTCACC T G tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1323440553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972707,Human_RBP_ID_1415120,Human_RBP_ID_5252964,Human_RBP_ID_5273285,Human_RBP_ID_5710284,Human_RBP_ID_8289878,Human_RBP_ID_9556181,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555622,Human_RBP_ID_19446039,Human_RBP_ID_21999637,Human_RBP_ID_22130936,Human_RBP_ID_22786834,Human_RBP_ID_22849847,Human_RBP_ID_23112693,Human_RBP_ID_23121725,Human_RBP_ID_23343520,Human_RBP_ID_26846452,Human_RBP_ID_27390926,Human_RBP_ID_27554640 63494 RMVar_ID_63494 Human_SNP_ID_4462605 m1A Human chr1 - 16545967 16545967 16545967 TTCAGTGGTAGAATTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAG TTCAGTGGTAGAATTCTCGCCTCCCACGCGGGGGACCCGGGTTCAATTCCCGGCCAATGCAAGAG T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:16545936..16546018 26863410 MeRIP-seq:(Medium) rs866626712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1415120,Human_RBP_ID_5710284,Human_RBP_ID_8289878,Human_RBP_ID_17072885,Human_RBP_ID_22871961,Human_RBP_ID_23121725,Human_RBP_ID_26872679 63495 RMVar_ID_63495 Human_SNP_ID_4462672 m1A Human chr1 - 16546013 16546013 16546013 GTTTTCTGTTATCCTGCAGGCGGTTGTTACGCAGAGGCATTGGTGGTTCAGTGGTAGAATTCTCG GTTTTCTGTTATCCTGCAGGCGGTTGTTACGCGGAGGCATTGGTGGTTCAGTGGTAGAATTCTCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16545934..16546021 26863410 MeRIP-seq:(Medium) rs1311580035 Functional Loss SNV dbSNP153 33..33 33 - - - 63496 RMVar_ID_63496 Human_SNP_ID_4462673 m1A Human chr1 - 16546013 16546013 16546013 GTTTTCTGTTATCCTGCAGGCGGTTGTTACGCAGAGGCATTGGTGGTTCAGTGGTAGAATTCTCG GTTTTCTGTTATCCTGCAGGCGGTTGTTACGCCGAGGCATTGGTGGTTCAGTGGTAGAATTCTCG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16545934..16546021 26863410 MeRIP-seq:(Medium) rs1311580035 Functional Loss SNV dbSNP153 33..33 33 - - - 63497 RMVar_ID_63497 Human_SNP_ID_4468549 m1A Human chr1 - 16562919 16562919 16562919 TGTTTATAGAGGACAGGTCAGCTCTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGT TGTTTATAGAGGACAGGTCAGCTCTCTGGCTCTATGATCTACATTCTGAAGTTGTCTGAAAATGT T A NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1215278941 Functional Loss SNV dbSNP153 33..33 33 - - - 63498 RMVar_ID_63498 Human_SNP_ID_4471309 m1A Human chr1 - 16569139 16569139 16569139 TCTCAATTCCTCCTGAAATGTTGGCCTCGTACAAGTCTTACAGCGGCACATTTCACTCATTAGAG TCTCAATTCCTCCTGAAATGTTGGCCTCGTACTAGTCTTACAGCGGCACATTTCACTCATTAGAG T A NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs849614 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_22534,Human_Splice_Rec_22535,Human_Splice_Rec_22588,Human_Splice_Rec_22589,Human_Splice_Rec_22624,Human_Splice_Rec_22625 Human_miRNA_ID_2657998,Human_miRNA_ID_2743256 RMVar_hsa_circ_107471,RMVar_hsa_circ_129548 63499 RMVar_ID_63499 Human_SNP_ID_4471310 m1A Human chr1 - 16569139 16569139 16569139 TCTCAATTCCTCCTGAAATGTTGGCCTCGTACAAGTCTTACAGCGGCACATTTCACTCATTAGAG TCTCAATTCCTCCTGAAATGTTGGCCTCGTACGAGTCTTACAGCGGCACATTTCACTCATTAGAG T C NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs849614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22534,Human_Splice_Rec_22535,Human_Splice_Rec_22588,Human_Splice_Rec_22589,Human_Splice_Rec_22624,Human_Splice_Rec_22625 Human_miRNA_ID_2657998,Human_miRNA_ID_2743256 RMVar_hsa_circ_107471,RMVar_hsa_circ_129548 63500 RMVar_ID_63500 Human_SNP_ID_4471311 m1A Human chr1 - 16569139 16569139 16569139 TCTCAATTCCTCCTGAAATGTTGGCCTCGTACAAGTCTTACAGCGGCACATTTCACTCATTAGAG TCTCAATTCCTCCTGAAATGTTGGCCTCGTACCAGTCTTACAGCGGCACATTTCACTCATTAGAG T G NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs849614 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_22534,Human_Splice_Rec_22535,Human_Splice_Rec_22588,Human_Splice_Rec_22589,Human_Splice_Rec_22624,Human_Splice_Rec_22625 Human_miRNA_ID_2657998,Human_miRNA_ID_2743256 RMVar_hsa_circ_107471,RMVar_hsa_circ_129548 63501 RMVar_ID_63501 Human_SNP_ID_4482421 m1A Human chr1 - 16589030 16589030 16589030 CAATATAAAGTCCTGGTTCACTCTCAGGAACGAGAGCTGACCCAGTTAAGGGAGAAGTTACGGGA CAATATAAAGTCCTGGTTCACTCTCAGGAACGGGAGCTGACCCAGTTAAGGGAGAAGTTACGGGA T C NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs201237274 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_22506,Human_Splice_Rec_22560 RMVar_hsa_circ_55378,RMVar_hsa_circ_67715,RMVar_hsa_circ_122744,RMVar_hsa_circ_125516,RMVar_hsa_circ_129552,RMVar_hsa_circ_129553 63502 RMVar_ID_63502 Human_SNP_ID_4492124 m1A Human chr1 - 16619912 16619912 16619912 CCGGCGGAAGGCTGAGAAGGAACAGCTGAGTGAGGAGATTGCTGCCCTGCAGCAGGAGCATGACG CCGGCGGAAGGCTGAGAAGGAACAGCTGAGTGCGGAGATTGCTGCCCTGCAGCAGGAGCATGACG T G CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16619095..16620036 26863196 MeRIP-seq:(Medium) rs10796418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332624,Human_RBP_ID_5538484,Human_RBP_ID_18415924 Human_Splice_Rec_22653,Human_Splice_Rec_22663,Human_Splice_Rec_22675,Human_Splice_Rec_22731 RMVar_hsa_circ_56321 63503 RMVar_ID_63503 Human_SNP_ID_4492492 m1A Human chr1 - 16621161 16621161 16621161 AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCATGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCGTGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11260839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5711081,Human_RBP_ID_8051634,Human_RBP_ID_8242521,Human_RBP_ID_9410452,Human_RBP_ID_18930564,Human_RBP_ID_21963551 RMVar_hsa_circ_56321 63504 RMVar_ID_63504 Human_SNP_ID_4492493 m1A Human chr1 - 16621161 16621161 16621161 AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCATGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCCTGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG T G CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11260839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5711081,Human_RBP_ID_8051634,Human_RBP_ID_8242521,Human_RBP_ID_9410452,Human_RBP_ID_18930564,Human_RBP_ID_21963551 RMVar_hsa_circ_56321 63505 RMVar_ID_63505 Human_SNP_ID_4492547 m1A Human chr1 - 16621342 16621342 16621342 GGCACTGGCATGCTCTCCAGAGTGGCCCTCAGAACAGGGGCCCTCAGCCACCAAATCCTAGACAG GGCACTGGCATGCTCTCCAGAGTGGCCCTCAGGACAGGGGCCCTCAGCCACCAAATCCTAGACAG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2786815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56321 63506 RMVar_ID_63506 Human_SNP_ID_4492984 m1A Human chr1 - 16623287 16623287 16623287 GATGGTTTTTAGATGATGGCTATACCATTTCCATTCCCTGTAGTCGTTTCCATTAATGCTGATAG GATGGTTTTTAGATGATGGCTATACCATTTCCGTTCCCTGTAGTCGTTTCCATTAATGCTGATAG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs9663022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1073995,Human_RBP_ID_1728842,Human_RBP_ID_3286186,Human_RBP_ID_5092196,Human_RBP_ID_8979439,Human_RBP_ID_10648524,Human_RBP_ID_17072771,Human_RBP_ID_17339878,Human_RBP_ID_18219558 RMVar_hsa_circ_56321 63507 RMVar_ID_63507 Human_SNP_ID_4493235 m1A Human chr1 - 16624273 16624273 16624273 CAGGACCGTGTCAGAGGAGGCCACACACCTGCAGTAAGGCCTTGGGCTCTGCCCAACCCGCCCTG CAGGACCGTGTCAGAGGAGGCCACACACCTGCGGTAAGGCCTTGGGCTCTGCCCAACCCGCCCTG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16624271..16624504 26863196 MeRIP-seq:(Medium) rs1557457773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10648545 Human_Splice_Rec_22725 RMVar_hsa_circ_56321 63508 RMVar_ID_63508 Human_SNP_ID_4493268 m1A Human chr1 - 16624370 16624365 16624371 GGTGGAGACGCTGGGGCAAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGGAGCACGCTGGCCTGG GGTGGAGACGCTGGGGCAAGTGGCCCGGGAG______GCGCTAGCCAAGGAGCACGCTGGCCTGG CCTCCTT C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16624359..16624459 26863196 MeRIP-seq:(Medium) rs1282185577 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_3335036,Human_RBP_ID_9271990,Human_RBP_ID_10648547,Human_RBP_ID_17204356,Human_RBP_ID_17672791,Human_RBP_ID_18475703,Human_RBP_ID_18926135 Human_Splice_Rec_22724,Human_Splice_Rec_22725 Human_miRNA_ID_1840865 RMVar_hsa_circ_56321 63509 RMVar_ID_63509 Human_SNP_ID_4493269 m1A Human chr1 - 16624370 16624368 16624371 GGTGGAGACGCTGGGGCAAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGGAGCACGCTGGCCTGG GGTGGAGACGCTGGGGCAAGTGGCCCGGGAG___GAGGCGCTAGCCAAGGAGCACGCTGGCCTGG CCTT C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16624359..16624459 26863196 MeRIP-seq:(Medium) rs1320810539 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3335036,Human_RBP_ID_9271990,Human_RBP_ID_10648547,Human_RBP_ID_17204356,Human_RBP_ID_17672791,Human_RBP_ID_18475703,Human_RBP_ID_18926135 Human_Splice_Rec_22724,Human_Splice_Rec_22725 Human_miRNA_ID_1840865 RMVar_hsa_circ_56321 63510 RMVar_ID_63510 Human_SNP_ID_4493274 m1A Human chr1 - 16624385 16624385 16624385 GGAGGCCCAGTGACAGGTGGAGACGCTGGGGCAAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGG GGAGGCCCAGTGACAGGTGGAGACGCTGGGGCGAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1629127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224886,Human_RBP_ID_3335036,Human_RBP_ID_5160911,Human_RBP_ID_8171564,Human_RBP_ID_9271990,Human_RBP_ID_9412782,Human_RBP_ID_10648547,Human_RBP_ID_17182579,Human_RBP_ID_17204356,Human_RBP_ID_17224440,Human_RBP_ID_17668418,Human_RBP_ID_18475703,Human_RBP_ID_18926135,Human_RBP_ID_21959340,Human_RBP_ID_21963756,Human_RBP_ID_22849914 Human_Splice_Rec_22724 RMVar_hsa_circ_56321 63511 RMVar_ID_63511 Human_SNP_ID_4494139 m1A Human chr1 - 16627191 16627191 16627191 GGAGGCGCTGAGCCGCGCCACGCTGCAACGGGACATGCTGCAGGCCGAGAAGACCGAGGTGGCCG GGAGGCGCTGAGCCGCGCCACGCTGCAACGGGGCATGCTGCAGGCCGAGAAGACCGAGGTGGCCG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16627114..16628637 26863196 MeRIP-seq:(Medium) rs1415451024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801622,Human_RBP_ID_853830,Human_RBP_ID_3932792,Human_RBP_ID_5538497,Human_RBP_ID_8242532,Human_RBP_ID_8755545,Human_RBP_ID_9355558,Human_RBP_ID_17456873,Human_RBP_ID_18964747,Human_RBP_ID_22871174,Human_RBP_ID_24541757,Human_RBP_ID_26310321 Human_Splice_Rec_22656,Human_Splice_Rec_22657,Human_Splice_Rec_22668,Human_Splice_Rec_22669,Human_Splice_Rec_22694,Human_Splice_Rec_22695,Human_Splice_Rec_22718,Human_Splice_Rec_22719,Human_Splice_Rec_22746,Human_Splice_Rec_22747 RMVar_hsa_circ_11074,RMVar_hsa_circ_73649,RMVar_hsa_circ_56321,RMVar_hsa_circ_33194,RMVar_hsa_circ_267494 63512 RMVar_ID_63512 Human_SNP_ID_4494143 m1A Human chr1 + 16627200 16627200 16627200 CGGTCTTCTCGGCCTGCAGCATGTCCCGTTGCAGCGTGGCGCGGCTCAGCGCCTCCCTCACCTCC CGGTCTTCTCGGCCTGCAGCATGTCCCGTTGCGGCGTGGCGCGGCTCAGCGCCTCCCTCACCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16627151..16628686 26863196 MeRIP-seq:(Medium) rs1212650434 Functional Loss SNV dbSNP153 33..33 33 - - - 63513 RMVar_ID_63513 Human_SNP_ID_4494559 m1A Human chr1 - 16628577 16628577 16628577 AGCAGGCCGAGGAGCTGCCGCAGGAGCGGGAGAAGCTGCAGGTTGCCCAGGAGGAGCTGCAGCGC AGCAGGCCGAGGAGCTGCCGCAGGAGCGGGAGGAGCTGCAGGTTGCCCAGGAGGAGCTGCAGCGC T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16628527..16629694 32194978 MeRIP-seq:(Medium) rs1391341009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853832,Human_RBP_ID_3935242,Human_RBP_ID_5538498,Human_RBP_ID_9355559,Human_RBP_ID_17730636,Human_RBP_ID_18523799,Human_RBP_ID_18967285 Human_Splice_Rec_22666,Human_Splice_Rec_22692,Human_Splice_Rec_22716,Human_Splice_Rec_22744 RMVar_hsa_circ_11074,RMVar_hsa_circ_33194 63514 RMVar_ID_63514 Human_SNP_ID_4495324 m1A Human chr1 - 16631017 16631017 16631017 CGGGGGCTCTCGGGCCAGCGGACCCCGTCTCCACCGCGGCGCTCCTCGCCGGGCCGAGGCCGTTC CGGGGGCTCTCGGGCCAGCGGACCCCGTCTCCCCCGCGGCGCTCCTCGCCGGGCCGAGGCCGTTC T G CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16630966..16631083 26863196 MeRIP-seq:(Medium) rs1325219662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4007469,Human_RBP_ID_5538506,Human_RBP_ID_8242534,Human_RBP_ID_8978597,Human_RBP_ID_9358142,Human_RBP_ID_18409157 Human_Splice_Rec_22690,Human_Splice_Rec_22712,Human_Splice_Rec_22742,Human_Splice_Rec_22760 RMVar_hsa_circ_11074,RMVar_hsa_circ_33194,RMVar_hsa_circ_18591,RMVar_hsa_circ_34197,RMVar_hsa_circ_45680,RMVar_hsa_circ_29922 63515 RMVar_ID_63515 Human_SNP_ID_4506674 m1A Human chr1 + 16678268 16678268 16678268 AGTAAAGAGCCATAGCGAAGTGAAAAACAACCACGTGCAGTGGCCGGGAATTGAACCCGGGTCTC AGTAAAGAGCCATAGCGAAGTGAAAAACAACCCCGTGCAGTGGCCGGGAATTGAACCCGGGTCTC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16678259..16678346 26863410 MeRIP-seq:(Medium) rs771367393 Functional Loss SNV dbSNP153 33..33 33 - - - 63516 RMVar_ID_63516 Human_SNP_ID_4506675 m1A Human chr1 + 16678268 16678268 16678268 AGTAAAGAGCCATAGCGAAGTGAAAAACAACCACGTGCAGTGGCCGGGAATTGAACCCGGGTCTC AGTAAAGAGCCATAGCGAAGTGAAAAACAACCGCGTGCAGTGGCCGGGAATTGAACCCGGGTCTC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16678259..16678346 26863410 MeRIP-seq:(Medium) rs771367393 Functional Loss SNV dbSNP153 33..33 33 - - - 63517 RMVar_ID_63517 Human_SNP_ID_4506689 m1A Human chr1 - 16678286 16678275 16678286 TTCTCGCCTCCCATGCGGGAGACCCGGGTTCAATTCCCGGCCACTGCACGTGGTTGTTTTTCACT TTCTCGCCTCCCATGCGGGAGACCCGGGTTCA___________CTGCACGTGGTTGTTTTTCACT GTGGCCGGGAAT G tRNA-Gly-CCC-4-1 RNACentral:URS00006B479B tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1042642077 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_332671,Human_RBP_ID_1415276,Human_RBP_ID_4084772,Human_RBP_ID_5254169,Human_RBP_ID_5272939,Human_RBP_ID_5413215,Human_RBP_ID_5456615,Human_RBP_ID_5484839,Human_RBP_ID_8240298,Human_RBP_ID_8290108,Human_RBP_ID_9466353,Human_RBP_ID_17341482,Human_RBP_ID_17675672,Human_RBP_ID_17730730,Human_RBP_ID_18555844,Human_RBP_ID_19223926,Human_RBP_ID_22017102,Human_RBP_ID_22131084,Human_RBP_ID_22781099,Human_RBP_ID_23121731,Human_RBP_ID_23145470,Human_RBP_ID_23302970,Human_RBP_ID_23344122,Human_RBP_ID_24455043,Human_RBP_ID_24754158,Human_RBP_ID_26371726,Human_RBP_ID_26846694,Human_RBP_ID_27171509 63518 RMVar_ID_63518 Human_SNP_ID_4506714 m1A Human chr1 - 16678286 16678286 16678286 TTCTCGCCTCCCATGCGGGAGACCCGGGTTCAATTCCCGGCCACTGCACGTGGTTGTTTTTCACT TTCTCGCCTCCCATGCGGGAGACCCGGGTTCATTTCCCGGCCACTGCACGTGGTTGTTTTTCACT T A tRNA-Gly-CCC-4-1 RNACentral:URS00006B479B tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs111541420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332671,Human_RBP_ID_1415276,Human_RBP_ID_4084772,Human_RBP_ID_5254169,Human_RBP_ID_5272939,Human_RBP_ID_5413215,Human_RBP_ID_5456615,Human_RBP_ID_5484839,Human_RBP_ID_8240298,Human_RBP_ID_8290108,Human_RBP_ID_9466353,Human_RBP_ID_17341482,Human_RBP_ID_17675672,Human_RBP_ID_17730730,Human_RBP_ID_18555844,Human_RBP_ID_19223926,Human_RBP_ID_22017102,Human_RBP_ID_22131084,Human_RBP_ID_22781099,Human_RBP_ID_23121731,Human_RBP_ID_23145470,Human_RBP_ID_23302970,Human_RBP_ID_23344122,Human_RBP_ID_24455043,Human_RBP_ID_24754158,Human_RBP_ID_26371726,Human_RBP_ID_26846694,Human_RBP_ID_27171509 63519 RMVar_ID_63519 Human_SNP_ID_4525640 m1A Human chr1 + 16727340 16727340 16727340 TTCTCGCCTCCCACGTGGGAGACCCGGGTTCAATTCCCGGCCAATGCAGCAGGTACTTCTTCATT TTCTCGCCTCCCACGTGGGAGACCCGGGTTCACTTCCCGGCCAATGCAGCAGGTACTTCTTCATT A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs113226545 Functional Loss SNV dbSNP153 33..33 33 - - - 63520 RMVar_ID_63520 Human_SNP_ID_4525641 m1A Human chr1 + 16727340 16727340 16727340 TTCTCGCCTCCCACGTGGGAGACCCGGGTTCAATTCCCGGCCAATGCAGCAGGTACTTCTTCATT TTCTCGCCTCCCACGTGGGAGACCCGGGTTCATTTCCCGGCCAATGCAGCAGGTACTTCTTCATT A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs113226545 Functional Loss SNV dbSNP153 33..33 33 - - - 63521 RMVar_ID_63521 Human_SNP_ID_4525642 m1A Human chr1 - 16727342 16727342 16727342 GAAATGAAGAAGTACCTGCTGCATTGGCCGGGAATTGAACCCGGGTCTCCCACGTGGGAGGCGAG GAAATGAAGAAGTACCTGCTGCATTGGCCGGGTATTGAACCCGGGTCTCCCACGTGGGAGGCGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:16727283..16727390;chr1:16727293..16727425;chr1:16727283..16727388;chr1:16727298..16727382 26863196 MeRIP-seq:(Medium) rs1356788438 Functional Loss SNV dbSNP153 33..33 33 - - - 63522 RMVar_ID_63522 Human_SNP_ID_4525661 m1A Human chr1 + 16727351 16727351 16727351 CACGTGGGAGACCCGGGTTCAATTCCCGGCCAATGCAGCAGGTACTTCTTCATTTCATTATGGCC CACGTGGGAGACCCGGGTTCAATTCCCGGCCACTGCAGCAGGTACTTCTTCATTTCATTATGGCC A C tRNA-Gly-CCC-5-1 RNACentral:URS00007131F2 tRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:16727274..16727413 26863196 MeRIP-seq:(Medium) rs1422924018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332703,Human_RBP_ID_1150525,Human_RBP_ID_1415305,Human_RBP_ID_1728951,Human_RBP_ID_2103752,Human_RBP_ID_3286394,Human_RBP_ID_5254284,Human_RBP_ID_5272946,Human_RBP_ID_5711906,Human_RBP_ID_8044331,Human_RBP_ID_8240304,Human_RBP_ID_8290138,Human_RBP_ID_17730754,Human_RBP_ID_18428917,Human_RBP_ID_18555859,Human_RBP_ID_22131094,Human_RBP_ID_22781105,Human_RBP_ID_22873055,Human_RBP_ID_23121740,Human_RBP_ID_26371739,Human_RBP_ID_26846712 63523 RMVar_ID_63523 Human_SNP_ID_4551287 m1A Human chr1 + 16861975 16861975 16861975 ATTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAAAGGGTCTTTTTCAC ATTCTCGCCTCCCACGCGGGAGACCCGGGTTCGATTCCCGGCCAATGCAAAAGGGTCTTTTTCAC A G CROCC Ensembl:ENSG00000058453 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1471276968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16541,Human_RBP_ID_220838,Human_RBP_ID_1415598,Human_RBP_ID_5273293,Human_RBP_ID_8171985,Human_RBP_ID_8755921,Human_RBP_ID_10654541,Human_RBP_ID_17762371,Human_RBP_ID_18545159,Human_RBP_ID_18926179,Human_RBP_ID_19225323,Human_RBP_ID_22781186,Human_RBP_ID_22871959,Human_RBP_ID_23121752,Human_RBP_ID_24400649,Human_RBP_ID_24541891,Human_RBP_ID_24550571,Human_RBP_ID_24556672,Human_RBP_ID_26753280 Human_miRNA_ID_2444740,Human_miRNA_ID_2446123 63524 RMVar_ID_63524 Human_SNP_ID_4551288 m1A Human chr1 + 16861976 16861976 16861976 TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAAAGGGTCTTTTTCACC TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAGTTCCCGGCCAATGCAAAAGGGTCTTTTTCACC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1193975676 Functional Loss SNV dbSNP153 33..33 33 - - - 63525 RMVar_ID_63525 Human_SNP_ID_4556113 m1A Human chr1 + 16872639 16872639 16872639 TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGATTCCCGGCCAGGGAATTGTTTTACACTGGCCG TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGCTTCCCGGCCAGGGAATTGTTTTACACTGGCCG A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1192156601 Functional Loss SNV dbSNP153 33..33 33 - - - 63526 RMVar_ID_63526 Human_SNP_ID_4565561 m1A Human chr1 + 16896044 16896044 16896044 CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCATTGCACTCCGGATGTGCTGACCCCTGCGATTT CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCCTTGCACTCCGGATGTGCTGACCCCTGCGATTT A C CROCC,RNU1-2 Ensembl:ENSG00000058453,Ensembl:ENSG00000207005 Protein coding,snRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1198567679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17457000,Human_RBP_ID_18174104,Human_RBP_ID_18198200,Human_RBP_ID_18205155,Human_RBP_ID_23110080,Human_RBP_ID_23112780,Human_RBP_ID_23117706,Human_RBP_ID_26747228,Human_RBP_ID_26872648 Human_miRNA_ID_2018329,Human_miRNA_ID_2023424,Human_miRNA_ID_2310045,Human_miRNA_ID_2312065,Human_miRNA_ID_2498154,Human_miRNA_ID_2605936,Human_miRNA_ID_2653840,Human_miRNA_ID_3127858,Human_miRNA_ID_3127965,Human_miRNA_ID_3131537,Human_miRNA_ID_3131614,Human_miRNA_ID_3135062,Human_miRNA_ID_3136806,Human_miRNA_ID_3137317 63527 RMVar_ID_63527 Human_SNP_ID_4565562 m1A Human chr1 + 16896044 16896044 16896044 CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCATTGCACTCCGGATGTGCTGACCCCTGCGATTT CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCGTTGCACTCCGGATGTGCTGACCCCTGCGATTT A G CROCC,RNU1-2 Ensembl:ENSG00000058453,Ensembl:ENSG00000207005 Protein coding,snRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1198567679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17457000,Human_RBP_ID_18174104,Human_RBP_ID_18198200,Human_RBP_ID_18205155,Human_RBP_ID_23110080,Human_RBP_ID_23112780,Human_RBP_ID_23117706,Human_RBP_ID_26747228,Human_RBP_ID_26872648 Human_miRNA_ID_2018329,Human_miRNA_ID_2023424,Human_miRNA_ID_2310045,Human_miRNA_ID_2312065,Human_miRNA_ID_2498154,Human_miRNA_ID_2605936,Human_miRNA_ID_2653840,Human_miRNA_ID_3127858,Human_miRNA_ID_3127965,Human_miRNA_ID_3131537,Human_miRNA_ID_3131614,Human_miRNA_ID_3135062,Human_miRNA_ID_3136806,Human_miRNA_ID_3137317 63528 RMVar_ID_63528 Human_SNP_ID_4565563 m1A Human chr1 + 16896044 16896044 16896044 CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCATTGCACTCCGGATGTGCTGACCCCTGCGATTT CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCTTTGCACTCCGGATGTGCTGACCCCTGCGATTT A T CROCC,RNU1-2 Ensembl:ENSG00000058453,Ensembl:ENSG00000207005 Protein coding,snRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1198567679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17457000,Human_RBP_ID_18174104,Human_RBP_ID_18198200,Human_RBP_ID_18205155,Human_RBP_ID_23110080,Human_RBP_ID_23112780,Human_RBP_ID_23117706,Human_RBP_ID_26747228,Human_RBP_ID_26872648 Human_miRNA_ID_2018329,Human_miRNA_ID_2023424,Human_miRNA_ID_2310045,Human_miRNA_ID_2312065,Human_miRNA_ID_2498154,Human_miRNA_ID_2605936,Human_miRNA_ID_2653840,Human_miRNA_ID_3127858,Human_miRNA_ID_3127965,Human_miRNA_ID_3131537,Human_miRNA_ID_3131614,Human_miRNA_ID_3135062,Human_miRNA_ID_3136806,Human_miRNA_ID_3137317 63529 RMVar_ID_63529 Human_SNP_ID_4574223 m1A Human chr1 - 16914139 16914129 16914139 GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTACCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC GCCCCCGCGCACGCGCGCGCCCCCGGCCACCT__________GCCTTCGCCGCAGCCGCTGCTGC CGCGCGAAGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:16914092..16914324;chr1:16914090..16914260 26863196 MeRIP-seq:(Medium) rs149234723 Functional Loss DEL dbSNP153 33..42 33 - - - 63530 RMVar_ID_63530 Human_SNP_ID_4574225 m1A Human chr1 + 16914135 16914129 16914135 CTCGGCAGCAGCGGCTGCGGCGAAGGCGCGCGAAGGTAGGTGGCCGGGGGCGCGCGCGTGCGCGG CTCGGCAGCAGCGGCTGCGGCGAAGGC______AGGTAGGTGGCCGGGGGCGCGCGCGTGCGCGG CGCGCGA C CROCC Ensembl:ENSG00000058453 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16914096..16914188 26863196 MeRIP-seq:(Medium) rs1557560087 Functional Loss DEL dbSNP153 28..33 33 - - - 63531 RMVar_ID_63531 Human_SNP_ID_4574231 m1A Human chr1 - 16914139 16914139 16914139 GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTACCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTTCCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:16914092..16914324;chr1:16914090..16914260 26863196 MeRIP-seq:(Medium) rs376567841 Functional Loss SNV dbSNP153 33..33 33 - - - 63532 RMVar_ID_63532 Human_SNP_ID_4574232 m1A Human chr1 - 16914139 16914139 16914139 GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTACCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTGCCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:16914092..16914324;chr1:16914090..16914260 26863196 MeRIP-seq:(Medium) rs376567841 Functional Loss SNV dbSNP153 33..33 33 - - - 63533 RMVar_ID_63533 Human_SNP_ID_4575662 m1A Human chr1 - 16918377 16918377 16918377 CCCCCAGAGTCCTGCTGGGTTCTGTGGGTCCCAGGAAGTCATATCTGAACCTCGTGTATGTGTCC CCCCCAGAGTCCTGCTGGGTTCTGTGGGTCCCCGGAAGTCATATCTGAACCTCGTGTATGTGTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16918374..16918561 26863196 MeRIP-seq:(Medium) rs1242421962 Functional Loss SNV dbSNP153 33..33 33 - - - 63534 RMVar_ID_63534 Human_SNP_ID_4579577 m1A Human chr1 + 16929850 16929850 16929850 GACTCTCACCCAGGGCCCTTCCCTGCAGCTGGAGCAGGCTCTGCGGCTGGAGCCTGGGGAGCTGG GACTCTCACCCAGGGCCCTTCCCTGCAGCTGGGGCAGGCTCTGCGGCTGGAGCCTGGGGAGCTGG A G CROCC Ensembl:ENSG00000058453 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16929848..16929949 26863196 MeRIP-seq:(Medium) rs1375954533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22858,Human_Splice_Rec_22972 RMVar_hsa_circ_61345,RMVar_hsa_circ_348073 63535 RMVar_ID_63535 Human_SNP_ID_4583201 m1A Human chr1 + 16938928 16938928 16938928 CCCCCACCCTCAGGCCGTCTTGTCAGACTCTGAGAGCGGCGTCCAGCTGAGCGGCTCTGAGCGCA CCCCCACCCTCAGGCCGTCTTGTCAGACTCTGGGAGCGGCGTCCAGCTGAGCGGCTCTGAGCGCA A G CROCC Ensembl:ENSG00000058453 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16937698..16938985 32194978 MeRIP-seq:(Medium) rs1446425235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801737 Human_Splice_Rec_22848,Human_Splice_Rec_22874,Human_Splice_Rec_22940,Human_Splice_Rec_22988,Human_Splice_Rec_23012,Human_Splice_Rec_23022 RMVar_hsa_circ_12853,RMVar_hsa_circ_348073,RMVar_hsa_circ_32253,RMVar_hsa_circ_20657,RMVar_hsa_circ_41161,RMVar_hsa_circ_49341 63536 RMVar_ID_63536 Human_SNP_ID_4585480 m1A Human chr1 + 16944195 16944195 16944195 GGAGCGGGAGAAGCTGCAGGCTGCCCAGGAGGAGCTGCGGCGCCAGCGGGACCGGCTGGAGGAAG GGAGCGGGAGAAGCTGCAGGCTGCCCAGGAGGGGCTGCGGCGCCAGCGGGACCGGCTGGAGGAAG A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16944146..16944251 26863196 MeRIP-seq:(Medium) rs1276266215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22878,Human_Splice_Rec_22879,Human_Splice_Rec_22944,Human_Splice_Rec_22945,Human_Splice_Rec_22992,Human_Splice_Rec_22993,Human_Splice_Rec_23016,Human_Splice_Rec_23017,Human_Splice_Rec_23026,Human_Splice_Rec_23027,Human_Splice_Rec_23035 63537 RMVar_ID_63537 Human_SNP_ID_4585917 m1A Human chr1 - 16945399 16945399 16945399 TGTCACTTTCCTGCCCCGAACCTCCTGTAGCCAGCGAGATGCTGGGCTGGGGACCAGGCCTGAGG TGTCACTTTCCTGCCCCGAACCTCCTGTAGCCGGCGAGATGCTGGGCTGGGGACCAGGCCTGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16945380..16945467 26863196 MeRIP-seq:(Medium) rs568299660 Functional Loss SNV dbSNP153 33..33 33 - - - 63538 RMVar_ID_63538 Human_SNP_ID_4586594 m1A Human chr1 + 16946841 16946841 16946841 CAGGAGGCCACAGTGGCGCGGGAAGAGCAGGAACGGCTAGAGGAGCTGCGGTTGGAGCAGGAGGT CAGGAGGCCACAGTGGCGCGGGAAGAGCAGGAGCGGCTAGAGGAGCTGCGGTTGGAGCAGGAGGT A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16946769..16947000 26863196 MeRIP-seq:(Medium) rs749626866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22884,Human_Splice_Rec_22950,Human_Splice_Rec_22998,Human_Splice_Rec_23032,Human_Splice_Rec_23040 63539 RMVar_ID_63539 Human_SNP_ID_4586601 m1A Human chr1 + 16946847 16946847 16946847 GCCACAGTGGCGCGGGAAGAGCAGGAACGGCTAGAGGAGCTGCGGTTGGAGCAGGAGGTGGCGCG GCCACAGTGGCGCGGGAAGAGCAGGAACGGCTGGAGGAGCTGCGGTTGGAGCAGGAGGTGGCGCG A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16946797..16948515 26863196 MeRIP-seq:(Medium) rs779480820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22884,Human_Splice_Rec_22950,Human_Splice_Rec_22998,Human_Splice_Rec_23032,Human_Splice_Rec_23040 63540 RMVar_ID_63540 Human_SNP_ID_4587316 m1A Human chr1 + 16948396 16948396 16948396 CTGGAGCAGGCCCGGCGGGAGGCCCAGCGGCAAGTGGAGGCGCTGGAGCGAGCGGCCCGTGAGAA CTGGAGCAGGCCCGGCGGGAGGCCCAGCGGCAGGTGGAGGCGCTGGAGCGAGCGGCCCGTGAGAA A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16948329..16948568 26863196 MeRIP-seq:(Medium) rs747322666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22886,Human_Splice_Rec_22952,Human_Splice_Rec_23044 63541 RMVar_ID_63541 Human_SNP_ID_4587320 m1A Human chr1 + 16948401 16948401 16948401 GCAGGCCCGGCGGGAGGCCCAGCGGCAAGTGGAGGCGCTGGAGCGAGCGGCCCGTGAGAAGGAGG GCAGGCCCGGCGGGAGGCCCAGCGGCAAGTGGGGGCGCTGGAGCGAGCGGCCCGTGAGAAGGAGG A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16946404..16951197 26863196 MeRIP-seq:(Medium) rs1234734669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22886,Human_Splice_Rec_22952,Human_Splice_Rec_23044 63542 RMVar_ID_63542 Human_SNP_ID_4588799 m1A Human chr1 - 16952695 16952695 16952695 GAGCTGGAGAGAACACAGATTTGGGGACATTAATGAGGCCAAGCCAGGCAATGCAAAGGGCAAGA GAGCTGGAGAGAACACAGATTTGGGGACATTATTGAGGCCAAGCCAGGCAATGCAAAGGGCAAGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:16952684..16952778 26863196 MeRIP-seq:(Medium) rs1425872962 Functional Loss SNV dbSNP153 33..33 33 - - - 63543 RMVar_ID_63543 Human_SNP_ID_4589025 m1A Human chr1 + 16953405 16953405 16953405 GCTGCTGGCCCGGCTGGAGGCTGAGAAGGAAGAGCTGAGTGAGGAGATTGCTGCCCTGCAGCAGG GCTGCTGGCCCGGCTGGAGGCTGAGAAGGAAGTGCTGAGTGAGGAGATTGCTGCCCTGCAGCAGG A T CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16953342..16953443 26863196 MeRIP-seq:(Medium) rs1327840964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22893,Human_Splice_Rec_22959,Human_Splice_Rec_23001,Human_Splice_Rec_23053 63544 RMVar_ID_63544 Human_SNP_ID_4591224 m1A Human chr1 - 16960919 16960919 16960919 TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCAGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCGGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16960870..16960971 26863196 MeRIP-seq:(Medium) rs2273113 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7725,GWAS_ID_7726 63545 RMVar_ID_63545 Human_SNP_ID_4591225 m1A Human chr1 - 16960919 16960919 16960919 TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCAGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCCGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16960870..16960971 26863196 MeRIP-seq:(Medium) rs2273113 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7725,GWAS_ID_7726 63546 RMVar_ID_63546 Human_SNP_ID_4593844 m1A Human chr1 + 16969269 16969268 16969269 AGGCCCTGGCCCAGAGCAGTGCCAGCCTCAACAGCACCCGGGACAAGAACCTGCATCTGCAGAAG AGGCCCTGGCCCAGAGCAGTGCCAGCCTCAAC_GCACCCGGGACAAGAACCTGCATCTGCAGAAG CA C CROCC Ensembl:ENSG00000058453 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1385106834 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_22915 63547 RMVar_ID_63547 Human_SNP_ID_4593845 m1A Human chr1 + 16969269 16969269 16969269 AGGCCCTGGCCCAGAGCAGTGCCAGCCTCAACAGCACCCGGGACAAGAACCTGCATCTGCAGAAG AGGCCCTGGCCCAGAGCAGTGCCAGCCTCAACGGCACCCGGGACAAGAACCTGCATCTGCAGAAG A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs56278097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22915 63548 RMVar_ID_63548 Human_SNP_ID_4593887 m1A Human chr1 - 16969356 16969356 16969356 GCTGACTCTCTCACTGGGCCCACCCCAGCCAGACCCTGGGCCCGAGACCTGGAGTACTTGGCGGT GCTGACTCTCTCACTGGGCCCACCCCAGCCAGGCCCTGGGCCCGAGACCTGGAGTACTTGGCGGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16969351..16969528 26863196 MeRIP-seq:(Medium) rs1323413056 Functional Loss SNV dbSNP153 33..33 33 - - - 63549 RMVar_ID_63549 Human_SNP_ID_4594099 m1A Human chr1 + 16969915 16969915 16969915 CCTGGAACTGCAGCGGGTGGAGGCCGAGGGCCAGCTACAACAGCTACGGGAGGTGAGGGCCAGGG CCTGGAACTGCAGCGGGTGGAGGCCGAGGGCCTGCTACAACAGCTACGGGAGGTGAGGGCCAGGG A T CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16969746..16970825 26863196 MeRIP-seq:(Medium) rs750293462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22917,Human_Splice_Rec_23065 63550 RMVar_ID_63550 Human_SNP_ID_4594740 m1A Human chr1 + 16971511 16971511 16971511 GCTGGAGCAGAGCCACAGCCCGGCCCAGCTGGAGGTGGATGCGCAGCAGCAGCAGCTGGAGCTGC GCTGGAGCAGAGCCACAGCCCGGCCCAGCTGGGGGTGGATGCGCAGCAGCAGCAGCTGGAGCTGC A G CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16971469..16971619 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_22922 63551 RMVar_ID_63551 Human_SNP_ID_4594741 m1A Human chr1 + 16971511 16971511 16971511 GCTGGAGCAGAGCCACAGCCCGGCCCAGCTGGAGGTGGATGCGCAGCAGCAGCAGCTGGAGCTGC GCTGGAGCAGAGCCACAGCCCGGCCCAGCTGGTGGTGGATGCGCAGCAGCAGCAGCTGGAGCTGC A T CROCC Ensembl:ENSG00000058453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16971469..16971619 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_22922 63552 RMVar_ID_63552 Human_SNP_ID_4598900 m1A Human chr1 + 16986188 16986188 16986188 AGAGGGGTCCAGTTGGTGGCTCAGAGGCAGGGAGTTCCAGTGTCTGGGGTGCCCGTGGGCCTGCA AGAGGGGTCCAGTTGGTGGCTCAGAGGCAGGGCGTTCCAGTGTCTGGGGTGCCCGTGGGCCTGCA A C AL049569.1 Ensembl:ENSG00000226526 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16986013..16986274 26863196 MeRIP-seq:(Medium) rs758219148 Functional Loss SNV dbSNP153 33..33 33 - - - 63553 RMVar_ID_63553 Human_SNP_ID_4602185 m1A Human chr1 + 16996082 16996082 16996082 TCCGCAGTCGGCTCTGGGCGTAGAGCGTGCACACAGTCATGGCAGCAGGCAGGGCAGGTGGCACC TCCGCAGTCGGCTCTGGGCGTAGAGCGTGCACGCAGTCATGGCAGCAGGCAGGGCAGGTGGCACC A G AL049569.1 Ensembl:ENSG00000226526 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16996032..16996149 26863196 MeRIP-seq:(Medium) rs201672021 Functional Loss SNV dbSNP153 33..33 33 - - - 63554 RMVar_ID_63554 Human_SNP_ID_4604886 m1A Human chr1 - 17004693 17004693 17004693 CCACAAGAGCGAGGAGGCGGTGAGTGTCGGACAGGTGGGTTCTGAAAAAGTCCTTGCCCCTCTCT CCACAAGAGCGAGGAGGCGGTGAGTGTCGGACGGGTGGGTTCTGAAAAAGTCCTTGCCCCTCTCT T C ATP13A2 Ensembl:ENSG00000159363 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17004691..17004847 26863196 MeRIP-seq:(Medium) rs779642983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_23337,Human_Splice_Rec_23545,Human_Splice_Rec_23559 RMVar_hsa_circ_102872,RMVar_hsa_circ_129577,RMVar_hsa_circ_23189 63555 RMVar_ID_63555 Human_SNP_ID_4605019 m1A Human chr1 + 17005063 17005063 17005063 CTCAGTCTGCACCTGGACAGTGAAGAGCTGCCAGGAACTATCCTGGAACACAGAGGTATGGACTC CTCAGTCTGCACCTGGACAGTGAAGAGCTGCCTGGAACTATCCTGGAACACAGAGGTATGGACTC A T AL049569.1 Ensembl:ENSG00000226526 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17004992..17005091 26863196 MeRIP-seq:(Medium) rs781539788 Functional Loss SNV dbSNP153 33..33 33 - - - 63556 RMVar_ID_63556 Human_SNP_ID_4611198 m1A Human chr1 - 17027798 17027797 17027798 TGAGCCTTATTTGAAGAAGAAGGATGAATCTCAGGAAGGCAAGCAGCAGTATCTGCAGTCCATAG TGAGCCTTATTTGAAGAAGAAGGATGAATCTC_GGAAGGCAAGCAGCAGTATCTGCAGTCCATAG CT C SDHB Ensembl:ENSG00000117118 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17027702..17027798 26863196 MeRIP-seq:(Medium) rs1553177678 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18539,Human_RBP_ID_333277,Human_RBP_ID_1415744,Human_RBP_ID_1729483,Human_RBP_ID_5714620,Human_RBP_ID_8290658,Human_RBP_ID_9355566,Human_RBP_ID_10656557,Human_RBP_ID_17647363,Human_RBP_ID_22024716,Human_RBP_ID_22430223,Human_RBP_ID_23345533,Human_RBP_ID_26313432 Human_Splice_Rec_23600,Human_Splice_Rec_23601,Human_Splice_Rec_23620,Human_Splice_Rec_23621,Human_Splice_Rec_23632,Human_Splice_Rec_23633,Human_Splice_Rec_23640,Human_Splice_Rec_23648 Clinvar_Rec_231 RMVar_hsa_circ_2558,RMVar_hsa_circ_112187,RMVar_hsa_circ_323190,RMVar_hsa_circ_334616,RMVar_hsa_circ_117796,RMVar_hsa_circ_129582,RMVar_hsa_circ_129584,RMVar_hsa_circ_129583 63557 RMVar_ID_63557 Human_SNP_ID_4611199 m1A Human chr1 - 17027798 17027798 17027798 TGAGCCTTATTTGAAGAAGAAGGATGAATCTCAGGAAGGCAAGCAGCAGTATCTGCAGTCCATAG TGAGCCTTATTTGAAGAAGAAGGATGAATCTCGGGAAGGCAAGCAGCAGTATCTGCAGTCCATAG T C SDHB Ensembl:ENSG00000117118 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17027702..17027798 26863196 MeRIP-seq:(Medium) rs747984404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18539,Human_RBP_ID_333277,Human_RBP_ID_1415744,Human_RBP_ID_1729483,Human_RBP_ID_5714620,Human_RBP_ID_8290658,Human_RBP_ID_9355566,Human_RBP_ID_10656557,Human_RBP_ID_17647363,Human_RBP_ID_22024716,Human_RBP_ID_22430223,Human_RBP_ID_23345533,Human_RBP_ID_26313432 Human_Splice_Rec_23600,Human_Splice_Rec_23601,Human_Splice_Rec_23620,Human_Splice_Rec_23621,Human_Splice_Rec_23632,Human_Splice_Rec_23633,Human_Splice_Rec_23640,Human_Splice_Rec_23648 RMVar_hsa_circ_2558,RMVar_hsa_circ_112187,RMVar_hsa_circ_323190,RMVar_hsa_circ_334616,RMVar_hsa_circ_117796,RMVar_hsa_circ_129582,RMVar_hsa_circ_129584,RMVar_hsa_circ_129583 63558 RMVar_ID_63558 Human_SNP_ID_4615551 m1A Human chr1 - 17044890 17044890 17044890 TTTTTTCCTTTTTGTGAACTTTAAAAAATTTCAGGCCTCCCGAGGAGCCCAGACAGCTGCAGCCA TTTTTTCCTTTTTGTGAACTTTAAAAAATTTCTGGCCTCCCGAGGAGCCCAGACAGCTGCAGCCA T A SDHB Ensembl:ENSG00000117118 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:17044801..17044955 26863410 MeRIP-seq:(Medium) rs1474282888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8958621,Human_RBP_ID_9269709 63559 RMVar_ID_63559 Human_SNP_ID_4617706 m1A Human chr1 - 17053425 17053425 17053425 GGGCAGGGGAAGGGAGAGATGGAGGGAAATGCACCCAGCCCCCTACCTCGAAGGATCCCGGAGGT GGGCAGGGGAAGGGAGAGATGGAGGGAAATGCTCCCAGCCCCCTACCTCGAAGGATCCCGGAGGT T A SDHB Ensembl:ENSG00000117118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:17053421..17053504 26863196 MeRIP-seq:(Medium) rs557945197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745985,Human_RBP_ID_23345720,Human_RBP_ID_24607499 63560 RMVar_ID_63560 Human_SNP_ID_4617850 m1A Human chr1 - 17053904 17053903 17053905 AGCCTCAGAGAGGGAAAAGTCAGGAAAGCCACAGAGACTGCCTGGAGCTGATGGGGCTGCGGAGA AGCCTCAGAGAGGGAAAAGTCAGGAAAGCCA__GAGACTGCCTGGAGCTGATGGGGCTGCGGAGA CTG C SDHB Ensembl:ENSG00000117118 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:17053902..17054050 26863410 MeRIP-seq:(Medium) rs910898144 Functional Loss DEL dbSNP153 32..33 33 - - - 63561 RMVar_ID_63561 Human_SNP_ID_4617924 m1A Human chr1 + 17053998 17053996 17053998 AAGGGTTGTGGCCGGCAACCGGCGCCTCAAGGAGAGGGCGACCACCGCCGCCATCTTGGCTCCTG AAGGGTTGTGGCCGGCAACCGGCGCCTCAAG__GAGGGCGACCACCGCCGCCATCTTGGCTCCTG GGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:17053897..17054121;chr1:17053903..17054091;chr1:17052464..17054127 26863196 MeRIP-seq:(Medium) rs1060503767 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_232 63562 RMVar_ID_63562 Human_SNP_ID_4617927 m1A Human chr1 + 17053998 17053998 17053998 AAGGGTTGTGGCCGGCAACCGGCGCCTCAAGGAGAGGGCGACCACCGCCGCCATCTTGGCTCCTG AAGGGTTGTGGCCGGCAACCGGCGCCTCAAGGGGAGGGCGACCACCGCCGCCATCTTGGCTCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:17053897..17054121;chr1:17053903..17054091;chr1:17052464..17054127 26863196 MeRIP-seq:(Medium) rs777447369 Functional Loss SNV dbSNP153 33..33 33 - - - 63563 RMVar_ID_63563 Human_SNP_ID_4713864 m1A Human chr1 + 17406937 17406937 17406937 CTTTCAAATTCTTTTTCCTGAGCTGGAAGACCAGTCAGATGCCCGCAGGGTCAGCGCCAAGCACA CTTTCAAATTCTTTTTCCTGAGCTGGAAGACCTGTCAGATGCCCGCAGGGTCAGCGCCAAGCACA A T RCC2-AS1 Ensembl:ENSG00000227751 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17406887..17406981 26863196 MeRIP-seq:(Medium) rs1260560322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_23891 63564 RMVar_ID_63564 Human_SNP_ID_4714047 m1A Human chr1 + 17407528 17407528 17407528 ATGCGCGTGGCGTCAGACTAAGTCTTAGAGAGATGCAGGCCAGTCTCCTCCCACAGGGCCTTGGG ATGCGCGTGGCGTCAGACTAAGTCTTAGAGAGTTGCAGGCCAGTCTCCTCCCACAGGGCCTTGGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:17407526..17407550 26863196 MeRIP-seq:(Medium) rs183352167 Functional Loss SNV dbSNP153 33..33 33 - - - 63565 RMVar_ID_63565 Human_SNP_ID_4714147 m1A Human chr1 + 17407927 17407927 17407927 AGGCGAGAGGAGGGTTCCGGGAAAGGCACCTCATAACTCACTCAGCGCAGCACACACGGCGGCGA AGGCGAGAGGAGGGTTCCGGGAAAGGCACCTCGTAACTCACTCAGCGCAGCACACACGGCGGCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17407876..17408033 26863196 MeRIP-seq:(Medium) rs1480382321 Functional Loss SNV dbSNP153 33..33 33 - - - 63566 RMVar_ID_63566 Human_SNP_ID_4714148 m1A Human chr1 + 17407927 17407927 17407927 AGGCGAGAGGAGGGTTCCGGGAAAGGCACCTCATAACTCACTCAGCGCAGCACACACGGCGGCGA AGGCGAGAGGAGGGTTCCGGGAAAGGCACCTCTTAACTCACTCAGCGCAGCACACACGGCGGCGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17407876..17408033 26863196 MeRIP-seq:(Medium) rs1480382321 Functional Loss SNV dbSNP153 33..33 33 - - - 63567 RMVar_ID_63567 Human_SNP_ID_4714153 m1A Human chr1 + 17407946 17407944 17407946 GGAAAGGCACCTCATAACTCACTCAGCGCAGCACACACGGCGGCGAGCTCGGGCACTTGACGAGG GGAAAGGCACCTCATAACTCACTCAGCGCAG__CACACGGCGGCGAGCTCGGGCACTTGACGAGG GCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:17407926..17407950 26863196 MeRIP-seq:(Medium) rs1416193371 Functional Loss DEL dbSNP153 32..33 33 - - - 63568 RMVar_ID_63568 Human_SNP_ID_4714343 m1A Human chr1 - 17408554 17408554 17408554 CCGGGTCACTCCTTCTCCGCTTTTTCTTGCAGATGGGCCTAGGCCGGTGTCGGTTCTGTTTCTCC CCGGGTCACTCCTTCTCCGCTTTTTCTTGCAGGTGGGCCTAGGCCGGTGTCGGTTCTGTTTCTCC T C RCC2 Ensembl:ENSG00000179051 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17408507..17408701 26863196 MeRIP-seq:(Medium) rs1178627045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333891,Human_RBP_ID_744214,Human_RBP_ID_1730042,Human_RBP_ID_3288071,Human_RBP_ID_5109429,Human_RBP_ID_5718727,Human_RBP_ID_8167709,Human_RBP_ID_10667714,Human_RBP_ID_17214046,Human_RBP_ID_17331728,Human_RBP_ID_17447832,Human_RBP_ID_18220208,Human_RBP_ID_18556890,Human_RBP_ID_22486486,Human_RBP_ID_24398391,Human_RBP_ID_24745132,Human_RBP_ID_26385388,Human_RBP_ID_27172031 Human_Splice_Rec_23918 RMVar_hsa_circ_113997,RMVar_hsa_circ_129589 63569 RMVar_ID_63569 Human_SNP_ID_4714513 m1A Human chr1 + 17409076 17409076 17409076 GACAGCTGCCGCGAGAGGTGTGGAGTCGGAGGAGTCTCCGGGAGCATCAGAGGGTTCGGGGGTTG GACAGCTGCCGCGAGAGGTGTGGAGTCGGAGGCGTCTCCGGGAGCATCAGAGGGTTCGGGGGTTG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:17409026..17409125 26863196 MeRIP-seq:(Medium) rs7531914 Functional Loss SNV dbSNP153 33..33 33 - - - 63570 RMVar_ID_63570 Human_SNP_ID_4720486 m1A Human chr1 - 17429199 17429199 17429199 CTAATTCTTTTTTCCTTTCTCTGTCTCTGCAGAAACTTGAAGGGTCAAAGTGCAAAGGGCAGCTT CTAATTCTTTTTTCCTTTCTCTGTCTCTGCAGCAACTTGAAGGGTCAAAGTGCAAAGGGCAGCTT T G RCC2 Ensembl:ENSG00000179051 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:17429151..17429200 26863196 MeRIP-seq:(Medium) rs375794587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25721,Human_RBP_ID_19231838 Human_Splice_Rec_23896,Human_Splice_Rec_23897,Human_Splice_Rec_23920,Human_Splice_Rec_23921 RMVar_hsa_circ_61879,RMVar_hsa_circ_129598,RMVar_hsa_circ_370367,RMVar_hsa_circ_320177 63571 RMVar_ID_63571 Human_SNP_ID_4723661 m1A Human chr1 - 17438382 17438370 17438382 GGAAGCGCGAGCGGCCCGAGCGCTGCAGTAGCAGCAGCGGCGGCGGCAGCAGCGGCGACGAGGAC GGAAGCGCGAGCGGCCCGAGCGCTGCAGTAGC____________GGCAGCAGCGGCGACGAGGAC CGCCGCCGCTGCT C RCC2 Ensembl:ENSG00000179051 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:17438122..17438625 26863196 MeRIP-seq:(Medium) rs1439520493 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_22532048 63572 RMVar_ID_63572 Human_SNP_ID_4724350 m1A Human chr1 - 17439890 17439890 17439890 GGCCCGCGAAAGGCGCAGGAGCAGCGGAGCCGAGGCGGGCGGCGAGGCGCGCGGCGCGCGGCGCA GGCCCGCGAAAGGCGCAGGAGCAGCGGAGCCGGGGCGGGCGGCGAGGCGCGCGGCGCGCGGCGCA T C MG828428 RNACentral:URS0000E29EAE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17439841..17439924 26863196 MeRIP-seq:(Medium) rs1180194543 Functional Loss SNV dbSNP153 33..33 33 - - - 63573 RMVar_ID_63573 Human_SNP_ID_4750621 m1A Human chr1 - 17539830 17539830 17539830 CCGCGGGCGCCCATGGCCGGGACGGCGCCCCCACCGCCGCAGCCGCCGCCACCCGAGCCAATGGC CCGCGGGCGCCCATGGCCGGGACGGCGCCCCCGCCGCCGCAGCCGCCGCCACCCGAGCCAATGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17539720..17540004 26863196 MeRIP-seq:(Medium) rs995029184 Functional Loss SNV dbSNP153 33..33 33 - - - 63574 RMVar_ID_63574 Human_SNP_ID_4750622 m1A Human chr1 - 17539830 17539830 17539830 CCGCGGGCGCCCATGGCCGGGACGGCGCCCCCACCGCCGCAGCCGCCGCCACCCGAGCCAATGGC CCGCGGGCGCCCATGGCCGGGACGGCGCCCCCCCCGCCGCAGCCGCCGCCACCCGAGCCAATGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17539720..17540004 26863196 MeRIP-seq:(Medium) rs995029184 Functional Loss SNV dbSNP153 33..33 33 - - - 63575 RMVar_ID_63575 Human_SNP_ID_4750629 m1A Human chr1 - 17539841 17539841 17539841 TCCGCAGGCCGCCGCGGGCGCCCATGGCCGGGACGGCGCCCCCACCGCCGCAGCCGCCGCCACCC TCCGCAGGCCGCCGCGGGCGCCCATGGCCGGGGCGGCGCCCCCACCGCCGCAGCCGCCGCCACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:17539707..17587569;chr1:17539732..17540021 26863196 MeRIP-seq:(Medium) rs1357851111 Functional Loss SNV dbSNP153 33..33 33 - - - 63576 RMVar_ID_63576 Human_SNP_ID_4758156 m1A Human chr1 + 17570925 17570925 17570925 TAGCAGCTGGTGGGATGGTGCTAGCAAGCGGGATGGGAAGACTGGGAGGAGCAGGGTTCTTTGTT TAGCAGCTGGTGGGATGGTGCTAGCAAGCGGGCTGGGAAGACTGGGAGGAGCAGGGTTCTTTGTT A C ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17570923..17571011 26863196 MeRIP-seq:(Medium) rs1250776338 Functional Loss SNV dbSNP153 33..33 33 - - - 63577 RMVar_ID_63577 Human_SNP_ID_4760351 m1A Human chr1 + 17580509 17580509 17580509 AGCCAGTGACTTGTCTCAGTAGCTGAAACTGCAGCCCTGACTCCAGCTAATGCGATTTCTGGTCT AGCCAGTGACTTGTCTCAGTAGCTGAAACTGCGGCCCTGACTCCAGCTAATGCGATTTCTGGTCT A G ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17580499..17580574 26863196 MeRIP-seq:(Medium) rs1198243342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189729,Human_RBP_ID_18414873,Human_RBP_ID_19036902,Human_RBP_ID_22534917,Human_RBP_ID_22635474 63578 RMVar_ID_63578 Human_SNP_ID_4760375 m1A Human chr1 - 17580605 17580605 17580605 GGTACCTATGGCAGGCTGTGGAGGAGGGTTGGAGGAAGCCATCAGACAAGGTCCAGCTCAGACCA GGTACCTATGGCAGGCTGTGGAGGAGGGTTGGTGGAAGCCATCAGACAAGGTCCAGCTCAGACCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:17580506..17580663;chr1:17580510..17580700 26863196 MeRIP-seq:(Medium) rs770501696 Functional Loss SNV dbSNP153 33..33 33 - - - 63579 RMVar_ID_63579 Human_SNP_ID_4762064 m1A Human chr1 + 17587415 17587415 17587415 CCCACCTACCCCAGCCATCTCTCCATTGACCAAACCTCGGAGATCCTGCAGCCTGGCCAACTCCT CCCACCTACCCCAGCCATCTCTCCATTGACCATACCTCGGAGATCCTGCAGCCTGGCCAACTCCT A T ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17587412..17587576 26863196 MeRIP-seq:(Medium) rs1399044631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129604,RMVar_hsa_circ_105645,RMVar_hsa_circ_356764,RMVar_hsa_circ_366518,RMVar_hsa_circ_369308,RMVar_hsa_circ_374767,RMVar_hsa_circ_374066,RMVar_hsa_circ_368458,RMVar_hsa_circ_364969,RMVar_hsa_circ_365299,RMVar_hsa_circ_364100,RMVar_hsa_circ_307941,RMVar_hsa_circ_341726,RMVar_hsa_circ_352166,RMVar_hsa_circ_308732,RMVar_hsa_circ_278452,RMVar_hsa_circ_285979,RMVar_hsa_circ_114033,RMVar_hsa_circ_60750,RMVar_hsa_circ_97653,RMVar_hsa_circ_99833,RMVar_hsa_circ_103281,RMVar_hsa_circ_87311,RMVar_hsa_circ_92359,RMVar_hsa_circ_87155,RMVar_hsa_circ_129608,RMVar_hsa_circ_129612,RMVar_hsa_circ_129616,RMVar_hsa_circ_129618,RMVar_hsa_circ_129620,RMVar_hsa_circ_129619,RMVar_hsa_circ_129617,RMVar_hsa_circ_129614,RMVar_hsa_circ_129615,RMVar_hsa_circ_129613,RMVar_hsa_circ_129610,RMVar_hsa_circ_129611,RMVar_hsa_circ_129609,RMVar_hsa_circ_129606,RMVar_hsa_circ_129607,RMVar_hsa_circ_129605,RMVar_hsa_circ_129600,RMVar_hsa_circ_129602,RMVar_hsa_circ_129603,RMVar_hsa_circ_129601 63580 RMVar_ID_63580 Human_SNP_ID_4762796 m1A Human chr1 + 17589784 17589783 17589784 TCTTCCAAGGGTTTATATCTCCAGGGTGGGCCAGGGGTGAAGTTGTGGAGAAACTCAGTCTGGTG TCTTCCAAGGGTTTATATCTCCAGGGTGGGCC_GGGGTGAAGTTGTGGAGAAACTCAGTCTGGTG CA C ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17589780..17589895 26863196 MeRIP-seq:(Medium) rs1318623977 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_129604,RMVar_hsa_circ_105645,RMVar_hsa_circ_356764,RMVar_hsa_circ_366518,RMVar_hsa_circ_369308,RMVar_hsa_circ_374066,RMVar_hsa_circ_368458,RMVar_hsa_circ_364969,RMVar_hsa_circ_365299,RMVar_hsa_circ_364100,RMVar_hsa_circ_307941,RMVar_hsa_circ_341726,RMVar_hsa_circ_352166,RMVar_hsa_circ_308732,RMVar_hsa_circ_285979,RMVar_hsa_circ_114033,RMVar_hsa_circ_60750,RMVar_hsa_circ_97653,RMVar_hsa_circ_99833,RMVar_hsa_circ_103281,RMVar_hsa_circ_87311,RMVar_hsa_circ_92359,RMVar_hsa_circ_87155,RMVar_hsa_circ_129608,RMVar_hsa_circ_129612,RMVar_hsa_circ_129616,RMVar_hsa_circ_129618,RMVar_hsa_circ_129617,RMVar_hsa_circ_129614,RMVar_hsa_circ_129615,RMVar_hsa_circ_129613,RMVar_hsa_circ_129610,RMVar_hsa_circ_129611,RMVar_hsa_circ_129609,RMVar_hsa_circ_129606,RMVar_hsa_circ_129607,RMVar_hsa_circ_129605,RMVar_hsa_circ_129600,RMVar_hsa_circ_129602,RMVar_hsa_circ_129603,RMVar_hsa_circ_129601,RMVar_hsa_circ_41013,RMVar_hsa_circ_364239,RMVar_hsa_circ_65696 63581 RMVar_ID_63581 Human_SNP_ID_4785110 m1A Human chr1 + 17676184 17676184 17676184 GTGTAGGTGCAGGCGTGGGTGCAGGTGTGGGTACAGGTGTAGGTGCAGGCATAGGTGCAGGTGTG GTGTAGGTGCAGGCGTGGGTGCAGGTGTGGGTGCAGGTGTAGGTGCAGGCATAGGTGCAGGTGTG A G ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:17675452..17676510;chr1:17675509..17676490 26863196 MeRIP-seq:(Medium) rs1263657245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8166787 RMVar_hsa_circ_369308,RMVar_hsa_circ_308732,RMVar_hsa_circ_114033,RMVar_hsa_circ_129600,RMVar_hsa_circ_129602,RMVar_hsa_circ_129601,RMVar_hsa_circ_101746,RMVar_hsa_circ_129627,RMVar_hsa_circ_350387,RMVar_hsa_circ_368942,RMVar_hsa_circ_362401 63582 RMVar_ID_63582 Human_SNP_ID_4790857 m1A Human chr1 + 17697187 17697187 17697187 GGAGGACGGCTCCATTTACGAGATGGCCGACGACCCCGACATCTGGGTGCGCAGCCGGCCCTGCG GGAGGACGGCTCCATTTACGAGATGGCCGACGGCCCCGACATCTGGGTGCGCAGCCGGCCCTGCG A G ARHGEF10L Ensembl:ENSG00000074964 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:17697136..17697235 26863196 MeRIP-seq:(Medium) rs777968170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114033,RMVar_hsa_circ_129600 63583 RMVar_ID_63583 Human_SNP_ID_5116683 m1A Human chr1 + 18956461 18956461 18956461 GGGCTCCAGCGCGGCCGGCCGGGCGGTTCCAGATGCGCGCCAGATGCGGCCTCCGCAGAGACGGC GGGCTCCAGCGCGGCCGGCCGGGCGGTTCCAGGTGCGCGCCAGATGCGGCCTCCGCAGAGACGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:18956402..18956654 26863196 MeRIP-seq:(Medium) rs1486834020 Functional Loss SNV dbSNP153 33..33 33 - - - 63584 RMVar_ID_63584 Human_SNP_ID_5147918 m1A Human chr1 - 19074819 19074819 19074819 TGTTGAACTCAGTCCCCTGACCACCACACAGCAGCTGCGGCGGCGAAGACGAAGCTGGCTTGCCT TGTTGAACTCAGTCCCCTGACCACCACACAGCGGCTGCGGCGGCGAAGACGAAGCTGGCTTGCCT T C AL137127.1,UBR4 Ensembl:ENSG00000272084,Ensembl:ENSG00000127481 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19074726..19074865 26863196 MeRIP-seq:(Medium) rs1234029581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801414,Human_RBP_ID_1074099,Human_RBP_ID_3333983,Human_RBP_ID_3932807,Human_RBP_ID_5092128,Human_RBP_ID_5109440,Human_RBP_ID_5537014,Human_RBP_ID_5890411,Human_RBP_ID_9253212,Human_RBP_ID_9269720,Human_RBP_ID_22026274 Human_Splice_Rec_24466,Human_Splice_Rec_24674,Human_Splice_Rec_24714,Human_Splice_Rec_24718,Human_Splice_Rec_24722 63585 RMVar_ID_63585 Human_SNP_ID_5148815 m1A Human chr1 + 19078064 19078064 19078064 AAGCGGAATAGTCCTTCACTGCCTTATCTGTCAGCCTGGAAAAGAAAATCCAGTTCCATCACATG AAGCGGAATAGTCCTTCACTGCCTTATCTGTCTGCCTGGAAAAGAAAATCCAGTTCCATCACATG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19074605..19078128 32194978 MeRIP-seq:(Medium) rs552106516 Functional Loss SNV dbSNP153 33..33 33 - - - 63586 RMVar_ID_63586 Human_SNP_ID_5153332 m1A Human chr1 - 19096650 19096650 19096650 TCCATTTCTGCTTGGCTTCCCTTCTCCCCTAGATGAAGAAGAAGATGAAGAAGAAGTGTATAAAA TCCATTTCTGCTTGGCTTCCCTTCTCCCCTAGGTGAAGAAGAAGATGAAGAAGAAGTGTATAAAA T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19096599..19099658 32194978 MeRIP-seq:(Medium) rs1029716001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742467,Human_RBP_ID_853924,Human_RBP_ID_1438106,Human_RBP_ID_3935275,Human_RBP_ID_4014242,Human_RBP_ID_9253219,Human_RBP_ID_18967404,Human_RBP_ID_24541414,Human_RBP_ID_26310332 Human_Splice_Rec_24646,Human_Splice_Rec_24686,Human_Splice_Rec_24730 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_106622,RMVar_hsa_circ_89377,RMVar_hsa_circ_117885,RMVar_hsa_circ_129651,RMVar_hsa_circ_129652,RMVar_hsa_circ_108109,RMVar_hsa_circ_86812,RMVar_hsa_circ_5329,RMVar_hsa_circ_129654,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_129655,RMVar_hsa_circ_111468,RMVar_hsa_circ_101513,RMVar_hsa_circ_120110,RMVar_hsa_circ_127389,RMVar_hsa_circ_129660,RMVar_hsa_circ_129661,RMVar_hsa_circ_125848,RMVar_hsa_circ_129662,RMVar_hsa_circ_129664,RMVar_hsa_circ_77668,RMVar_hsa_circ_129665,RMVar_hsa_circ_129663,RMVar_hsa_circ_118790,RMVar_hsa_circ_129666,RMVar_hsa_circ_102084,RMVar_hsa_circ_266689,RMVar_hsa_circ_40296,RMVar_hsa_circ_129667 63587 RMVar_ID_63587 Human_SNP_ID_5159743 m1A Human chr1 - 19123000 19123000 19123000 TGCGCCGTCAAGTCCGCAAACTTCTGCTCTTCATCTGTGGATCCAAAGAGAAGTACCGCCAGCTC TGCGCCGTCAAGTCCGCAAACTTCTGCTCTTCCTCTGTGGATCCAAAGAGAAGTACCGCCAGCTC T G UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19122949..19123050 32194978 MeRIP-seq:(Medium) rs1346653609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1732270,Human_RBP_ID_8739927,Human_RBP_ID_9269794,Human_RBP_ID_10710364,Human_RBP_ID_22532051 Human_Splice_Rec_24594,Human_Splice_Rec_24790,Human_Splice_Rec_24868 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_106622,RMVar_hsa_circ_89377,RMVar_hsa_circ_129651,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_111468,RMVar_hsa_circ_101513,RMVar_hsa_circ_120110,RMVar_hsa_circ_127389,RMVar_hsa_circ_129660,RMVar_hsa_circ_129661,RMVar_hsa_circ_125848,RMVar_hsa_circ_129662,RMVar_hsa_circ_129664,RMVar_hsa_circ_129663,RMVar_hsa_circ_118790,RMVar_hsa_circ_129667,RMVar_hsa_circ_265971,RMVar_hsa_circ_75603,RMVar_hsa_circ_129668,RMVar_hsa_circ_267426,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_124433,RMVar_hsa_circ_129670,RMVar_hsa_circ_129672,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_115229,RMVar_hsa_circ_265689,RMVar_hsa_circ_94349,RMVar_hsa_circ_129673,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_129674,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_94696,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_129679,RMVar_hsa_circ_103221,RMVar_hsa_circ_68682,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_79227,RMVar_hsa_circ_129682,RMVar_hsa_circ_129680,RMVar_hsa_circ_55383,RMVar_hsa_circ_50626,RMVar_hsa_circ_18229,RMVar_hsa_circ_108348,RMVar_hsa_circ_129685,RMVar_hsa_circ_80182,RMVar_hsa_circ_123360,RMVar_hsa_circ_129684,RMVar_hsa_circ_81223,RMVar_hsa_circ_129686,RMVar_hsa_circ_129687,RMVar_hsa_circ_84928,RMVar_hsa_circ_128134,RMVar_hsa_circ_129688,RMVar_hsa_circ_129689,RMVar_hsa_circ_75576,RMVar_hsa_circ_129690,RMVar_hsa_circ_14627 63588 RMVar_ID_63588 Human_SNP_ID_5163538 m1A Human chr1 + 19139040 19139040 19139040 AAGACCCAAGCAGAGATTCCTGTTTTGTCCCCACCCTCTGCCCAAGGAGACAGGACCCCCGCCAT AAGACCCAAGCAGAGATTCCTGTTTTGTCCCCCCCCTCTGCCCAAGGAGACAGGACCCCCGCCAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19139038..19139153 26863196 MeRIP-seq:(Medium) rs752425699 Functional Loss SNV dbSNP153 33..33 33 - - - 63589 RMVar_ID_63589 Human_SNP_ID_5164167 m1A Human chr1 + 19141483 19141483 19141483 GCCAGCAGGGCCTCCAGGGGAGAGGGGTTGCCATTGTTGACATTTTCAGCTGTCTCCAGGACCAT GCCAGCAGGGCCTCCAGGGGAGAGGGGTTGCCTTTGTTGACATTTTCAGCTGTCTCCAGGACCAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19141315..19141546 26863196 MeRIP-seq:(Medium) rs12068417 Functional Loss SNV dbSNP153 33..33 33 - - - 63590 RMVar_ID_63590 Human_SNP_ID_5164242 m1A Human chr1 - 19141696 19141696 19141696 ATCAGGGATCCCGAATGGTGGTCACATCCGTCAGGAAAGCCAGGAACAGAGTGAGGTGGACCATG ATCAGGGATCCCGAATGGTGGTCACATCCGTCGGGAAAGCCAGGAACAGAGTGAGGTGGACCATG T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19141623..19141736 26863196 MeRIP-seq:(Medium) rs759903656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932870,Human_RBP_ID_4014443,Human_RBP_ID_5518547,Human_RBP_ID_8753652,Human_RBP_ID_9271093,Human_RBP_ID_17762382,Human_RBP_ID_18964870,Human_RBP_ID_26313462,Human_RBP_ID_27799681 Human_Splice_Rec_24574,Human_Splice_Rec_24575,Human_Splice_Rec_24772,Human_Splice_Rec_24773,Human_Splice_Rec_24850,Human_Splice_Rec_24851 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_111468,RMVar_hsa_circ_101513,RMVar_hsa_circ_120110,RMVar_hsa_circ_127389,RMVar_hsa_circ_129660,RMVar_hsa_circ_129661,RMVar_hsa_circ_125848,RMVar_hsa_circ_129662,RMVar_hsa_circ_129664,RMVar_hsa_circ_129663,RMVar_hsa_circ_118790,RMVar_hsa_circ_129667,RMVar_hsa_circ_265971,RMVar_hsa_circ_75603,RMVar_hsa_circ_129668,RMVar_hsa_circ_267426,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_124433,RMVar_hsa_circ_129670,RMVar_hsa_circ_129672,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_115229,RMVar_hsa_circ_265689,RMVar_hsa_circ_94349,RMVar_hsa_circ_129673,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_129674,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_94696,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_129679,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_79227,RMVar_hsa_circ_129682,RMVar_hsa_circ_129680,RMVar_hsa_circ_50626,RMVar_hsa_circ_108348,RMVar_hsa_circ_129685,RMVar_hsa_circ_80182,RMVar_hsa_circ_123360,RMVar_hsa_circ_129684,RMVar_hsa_circ_81223,RMVar_hsa_circ_129686,RMVar_hsa_circ_129687,RMVar_hsa_circ_84928,RMVar_hsa_circ_128134,RMVar_hsa_circ_129688,RMVar_hsa_circ_129689,RMVar_hsa_circ_75576,RMVar_hsa_circ_94360,RMVar_hsa_circ_118805,RMVar_hsa_circ_129690,RMVar_hsa_circ_14627,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129693,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_82336,RMVar_hsa_circ_129700,RMVar_hsa_circ_42107,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_129703,RMVar_hsa_circ_372463,RMVar_hsa_circ_320327,RMVar_hsa_circ_108532,RMVar_hsa_circ_129704,RMVar_hsa_circ_12072,RMVar_hsa_circ_91536,RMVar_hsa_circ_129706,RMVar_hsa_circ_129707,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_78660,RMVar_hsa_circ_129709,RMVar_hsa_circ_129710 63591 RMVar_ID_63591 Human_SNP_ID_5165777 m1A Human chr1 - 19146883 19146883 19146883 GGCTAGTGATCACAGCTCGCTCCATTGCCATCATGCGCCCCAACAACCTTGTCCACTTTACGGAG GGCTAGTGATCACAGCTCGCTCCATTGCCATCTTGCGCCCCAACAACCTTGTCCACTTTACGGAG T A UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19146833..19146932 26863196 MeRIP-seq:(Medium) rs763606759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518554,Human_RBP_ID_9252726 Human_Splice_Rec_24567,Human_Splice_Rec_24765,Human_Splice_Rec_24843 Human_miRNA_ID_2941350 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_111468,RMVar_hsa_circ_129661,RMVar_hsa_circ_118790,RMVar_hsa_circ_129667,RMVar_hsa_circ_75603,RMVar_hsa_circ_267426,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_124433,RMVar_hsa_circ_129670,RMVar_hsa_circ_129672,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_115229,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_129674,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_94696,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_129679,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_79227,RMVar_hsa_circ_129682,RMVar_hsa_circ_129680,RMVar_hsa_circ_50626,RMVar_hsa_circ_80182,RMVar_hsa_circ_81223,RMVar_hsa_circ_129686,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_75576,RMVar_hsa_circ_94360,RMVar_hsa_circ_129690,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_80950,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_108532,RMVar_hsa_circ_129704,RMVar_hsa_circ_91536,RMVar_hsa_circ_129706,RMVar_hsa_circ_129707,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_101251,RMVar_hsa_circ_99134,RMVar_hsa_circ_129710,RMVar_hsa_circ_129712,RMVar_hsa_circ_360718,RMVar_hsa_circ_91770,RMVar_hsa_circ_113220,RMVar_hsa_circ_113699,RMVar_hsa_circ_129713,RMVar_hsa_circ_104931,RMVar_hsa_circ_96918,RMVar_hsa_circ_97662,RMVar_hsa_circ_82849,RMVar_hsa_circ_129714,RMVar_hsa_circ_129718,RMVar_hsa_circ_129720,RMVar_hsa_circ_129722,RMVar_hsa_circ_79414,RMVar_hsa_circ_129721,RMVar_hsa_circ_129719,RMVar_hsa_circ_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715 63592 RMVar_ID_63592 Human_SNP_ID_5165778 m1A Human chr1 - 19146883 19146883 19146883 GGCTAGTGATCACAGCTCGCTCCATTGCCATCATGCGCCCCAACAACCTTGTCCACTTTACGGAG GGCTAGTGATCACAGCTCGCTCCATTGCCATCGTGCGCCCCAACAACCTTGTCCACTTTACGGAG T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19146833..19146932 26863196 MeRIP-seq:(Medium) rs763606759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518554,Human_RBP_ID_9252726 Human_Splice_Rec_24567,Human_Splice_Rec_24765,Human_Splice_Rec_24843 Human_miRNA_ID_2941350 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_111468,RMVar_hsa_circ_129661,RMVar_hsa_circ_118790,RMVar_hsa_circ_129667,RMVar_hsa_circ_75603,RMVar_hsa_circ_267426,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_124433,RMVar_hsa_circ_129670,RMVar_hsa_circ_129672,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_115229,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_129674,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_94696,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_129679,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_79227,RMVar_hsa_circ_129682,RMVar_hsa_circ_129680,RMVar_hsa_circ_50626,RMVar_hsa_circ_80182,RMVar_hsa_circ_81223,RMVar_hsa_circ_129686,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_75576,RMVar_hsa_circ_94360,RMVar_hsa_circ_129690,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_80950,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_108532,RMVar_hsa_circ_129704,RMVar_hsa_circ_91536,RMVar_hsa_circ_129706,RMVar_hsa_circ_129707,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_101251,RMVar_hsa_circ_99134,RMVar_hsa_circ_129710,RMVar_hsa_circ_129712,RMVar_hsa_circ_360718,RMVar_hsa_circ_91770,RMVar_hsa_circ_113220,RMVar_hsa_circ_113699,RMVar_hsa_circ_129713,RMVar_hsa_circ_104931,RMVar_hsa_circ_96918,RMVar_hsa_circ_97662,RMVar_hsa_circ_82849,RMVar_hsa_circ_129714,RMVar_hsa_circ_129718,RMVar_hsa_circ_129720,RMVar_hsa_circ_129722,RMVar_hsa_circ_79414,RMVar_hsa_circ_129721,RMVar_hsa_circ_129719,RMVar_hsa_circ_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715 63593 RMVar_ID_63593 Human_SNP_ID_5165779 m1A Human chr1 - 19146883 19146883 19146883 GGCTAGTGATCACAGCTCGCTCCATTGCCATCATGCGCCCCAACAACCTTGTCCACTTTACGGAG GGCTAGTGATCACAGCTCGCTCCATTGCCATCCTGCGCCCCAACAACCTTGTCCACTTTACGGAG T G UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19146833..19146932 26863196 MeRIP-seq:(Medium) rs763606759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518554,Human_RBP_ID_9252726 Human_Splice_Rec_24567,Human_Splice_Rec_24765,Human_Splice_Rec_24843 Human_miRNA_ID_2941350 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_111468,RMVar_hsa_circ_129661,RMVar_hsa_circ_118790,RMVar_hsa_circ_129667,RMVar_hsa_circ_75603,RMVar_hsa_circ_267426,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_124433,RMVar_hsa_circ_129670,RMVar_hsa_circ_129672,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_115229,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_129674,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_94696,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_129679,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_79227,RMVar_hsa_circ_129682,RMVar_hsa_circ_129680,RMVar_hsa_circ_50626,RMVar_hsa_circ_80182,RMVar_hsa_circ_81223,RMVar_hsa_circ_129686,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_75576,RMVar_hsa_circ_94360,RMVar_hsa_circ_129690,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_80950,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_108532,RMVar_hsa_circ_129704,RMVar_hsa_circ_91536,RMVar_hsa_circ_129706,RMVar_hsa_circ_129707,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_101251,RMVar_hsa_circ_99134,RMVar_hsa_circ_129710,RMVar_hsa_circ_129712,RMVar_hsa_circ_360718,RMVar_hsa_circ_91770,RMVar_hsa_circ_113220,RMVar_hsa_circ_113699,RMVar_hsa_circ_129713,RMVar_hsa_circ_104931,RMVar_hsa_circ_96918,RMVar_hsa_circ_97662,RMVar_hsa_circ_82849,RMVar_hsa_circ_129714,RMVar_hsa_circ_129718,RMVar_hsa_circ_129720,RMVar_hsa_circ_129722,RMVar_hsa_circ_79414,RMVar_hsa_circ_129721,RMVar_hsa_circ_129719,RMVar_hsa_circ_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715 63594 RMVar_ID_63594 Human_SNP_ID_5167076 m1A Human chr1 + 19151648 19151648 19151648 AGTCTGCACCAGGGGTTGGTGACTCACTGAAGAGGTTCAGCTTCTTATCAGCCTGCAGGGCTTCT AGTCTGCACCAGGGGTTGGTGACTCACTGAAGGGGTTCAGCTTCTTATCAGCCTGCAGGGCTTCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19151645..19152348 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 63595 RMVar_ID_63595 Human_SNP_ID_5168640 m1A Human chr1 - 19157974 19157974 19157974 CTTTGCCAGGTTCCCACCTTAGGGTCCCAGGAAGGTGCCTTTGAGAATGTGCGGATGAATTACAG CTTTGCCAGGTTCCCACCTTAGGGTCCCAGGAGGGTGCCTTTGAGAATGTGCGGATGAATTACAG T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19157925..19158037 26863196 MeRIP-seq:(Medium) rs1229905575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19448,Human_RBP_ID_849550,Human_RBP_ID_1732303,Human_RBP_ID_3932886,Human_RBP_ID_5458283,Human_RBP_ID_5518590,Human_RBP_ID_8228215,Human_RBP_ID_8753674,Human_RBP_ID_9271128,Human_RBP_ID_10710855,Human_RBP_ID_18468487,Human_RBP_ID_18558949,Human_RBP_ID_18964889,Human_RBP_ID_23353360,Human_RBP_ID_24746550,Human_RBP_ID_26315785 Human_Splice_Rec_24544,Human_Splice_Rec_24818,Human_Splice_Rec_24922 Human_miRNA_ID_1963039,Human_miRNA_ID_2038263,Human_miRNA_ID_2762475,Human_miRNA_ID_3017243 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_75603,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_129670,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_129682,RMVar_hsa_circ_50626,RMVar_hsa_circ_81223,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_94360,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_19928,RMVar_hsa_circ_80950,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_129704,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_101251,RMVar_hsa_circ_99134,RMVar_hsa_circ_129710,RMVar_hsa_circ_129712,RMVar_hsa_circ_91770,RMVar_hsa_circ_113220,RMVar_hsa_circ_129713,RMVar_hsa_circ_104931,RMVar_hsa_circ_96918,RMVar_hsa_circ_129714,RMVar_hsa_circ_129718,RMVar_hsa_circ_79414,RMVar_hsa_circ_129719,RMVar_hsa_circ_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715,RMVar_hsa_circ_117238,RMVar_hsa_circ_92038,RMVar_hsa_circ_129724,RMVar_hsa_circ_129725,RMVar_hsa_circ_90608,RMVar_hsa_circ_129727,RMVar_hsa_circ_370275,RMVar_hsa_circ_377953,RMVar_hsa_circ_112685,RMVar_hsa_circ_110459,RMVar_hsa_circ_129730,RMVar_hsa_circ_102277,RMVar_hsa_circ_7421,RMVar_hsa_circ_129732,RMVar_hsa_circ_129731,RMVar_hsa_circ_129728,RMVar_hsa_circ_129729,RMVar_hsa_circ_120476,RMVar_hsa_circ_60952,RMVar_hsa_circ_119383,RMVar_hsa_circ_378523,RMVar_hsa_circ_129736,RMVar_hsa_circ_293987,RMVar_hsa_circ_109927,RMVar_hsa_circ_129739,RMVar_hsa_circ_129740,RMVar_hsa_circ_129738,RMVar_hsa_circ_129741,RMVar_hsa_circ_113840 63596 RMVar_ID_63596 Human_SNP_ID_5169184 m1A Human chr1 - 19160142 19160142 19160142 TCAGCAAGCCCTCAGTGAGCTACACACTGTGGAGAAGGCAGTGGAGATGACAGACCAGCTGATGG TCAGCAAGCCCTCAGTGAGCTACACACTGTGGGGAAGGCAGTGGAGATGACAGACCAGCTGATGG T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:19160101..19160200 26863196 MeRIP-seq:(Medium) rs1406357719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804476,Human_RBP_ID_1732304,Human_RBP_ID_3935340,Human_RBP_ID_5518593,Human_RBP_ID_5537058,Human_RBP_ID_18964890 Human_Splice_Rec_24543,Human_Splice_Rec_24817,Human_Splice_Rec_24921 Human_miRNA_ID_2966965 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,RMVar_hsa_circ_86812,RMVar_hsa_circ_129656,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_129657,RMVar_hsa_circ_75603,RMVar_hsa_circ_129669,RMVar_hsa_circ_103923,RMVar_hsa_circ_129670,RMVar_hsa_circ_87791,RMVar_hsa_circ_88777,RMVar_hsa_circ_107674,RMVar_hsa_circ_129675,RMVar_hsa_circ_129676,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_125294,RMVar_hsa_circ_129678,RMVar_hsa_circ_108628,RMVar_hsa_circ_103221,RMVar_hsa_circ_129681,RMVar_hsa_circ_129683,RMVar_hsa_circ_129682,RMVar_hsa_circ_50626,RMVar_hsa_circ_81223,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_94360,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_113247,RMVar_hsa_circ_115065,RMVar_hsa_circ_102844,RMVar_hsa_circ_129697,RMVar_hsa_circ_85355,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_129695,RMVar_hsa_circ_129696,RMVar_hsa_circ_129694,RMVar_hsa_circ_19928,RMVar_hsa_circ_80950,RMVar_hsa_circ_10777,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_123507,RMVar_hsa_circ_129704,RMVar_hsa_circ_129705,RMVar_hsa_circ_100435,RMVar_hsa_circ_101251,RMVar_hsa_circ_99134,RMVar_hsa_circ_129710,RMVar_hsa_circ_129712,RMVar_hsa_circ_91770,RMVar_hsa_circ_113220,RMVar_hsa_circ_129713,RMVar_hsa_circ_104931,RMVar_hsa_circ_96918,RMVar_hsa_circ_129714,RMVar_hsa_circ_129718,RMVar_hsa_circ_79414,RMVar_hsa_circ_129719,RMVar_hsa_circ_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715,RMVar_hsa_circ_117238,RMVar_hsa_circ_92038,RMVar_hsa_circ_129724,RMVar_hsa_circ_129725,RMVar_hsa_circ_90608,RMVar_hsa_circ_129727,RMVar_hsa_circ_370275,RMVar_hsa_circ_377953,RMVar_hsa_circ_112685,RMVar_hsa_circ_110459,RMVar_hsa_circ_129730,RMVar_hsa_circ_102277,RMVar_hsa_circ_129732,RMVar_hsa_circ_129731,RMVar_hsa_circ_129728,RMVar_hsa_circ_129729,RMVar_hsa_circ_120476,RMVar_hsa_circ_21863,RMVar_hsa_circ_79176,RMVar_hsa_circ_60952,RMVar_hsa_circ_119383,RMVar_hsa_circ_378523,RMVar_hsa_circ_129736,RMVar_hsa_circ_293987,RMVar_hsa_circ_109927,RMVar_hsa_circ_129739,RMVar_hsa_circ_129740,RMVar_hsa_circ_129738,RMVar_hsa_circ_123768,RMVar_hsa_circ_129741,RMVar_hsa_circ_113840,RMVar_hsa_circ_348402,RMVar_hsa_circ_101270,RMVar_hsa_circ_56149,RMVar_hsa_circ_60243,RMVar_hsa_circ_55599,RMVar_hsa_circ_129742,RMVar_hsa_circ_129743,RMVar_hsa_circ_129744 63597 RMVar_ID_63597 Human_SNP_ID_5176154 m1A Human chr1 - 19187154 19187154 19187154 TACTTTCAACTTCCTACAGAAAGGTGGGTGGGAGTTAAGCCATTGATAATTTAGAAGAATGTCTC TACTTTCAACTTCCTACAGAAAGGTGGGTGGGCGTTAAGCCATTGATAATTTAGAAGAATGTCTC T G UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19187151..19187200 32194978 MeRIP-seq:(Medium) rs1275600409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85305,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_103923,RMVar_hsa_circ_129670,RMVar_hsa_circ_87791,RMVar_hsa_circ_107674,RMVar_hsa_circ_129676,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_103221,RMVar_hsa_circ_129683,RMVar_hsa_circ_129682,RMVar_hsa_circ_81223,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_102844,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_108770,RMVar_hsa_circ_129702,RMVar_hsa_circ_100435,RMVar_hsa_circ_129710,RMVar_hsa_circ_113220,RMVar_hsa_circ_96918,RMVar_hsa_circ_129714,RMVar_hsa_circ_79414,RMVar_hsa_circ_129716,RMVar_hsa_circ_129715,RMVar_hsa_circ_377953,RMVar_hsa_circ_110459,RMVar_hsa_circ_129728,RMVar_hsa_circ_129729,RMVar_hsa_circ_79176,RMVar_hsa_circ_129742,RMVar_hsa_circ_129751,RMVar_hsa_circ_94494,RMVar_hsa_circ_27446,RMVar_hsa_circ_129755,RMVar_hsa_circ_93158,RMVar_hsa_circ_107229,RMVar_hsa_circ_69721,RMVar_hsa_circ_123901,RMVar_hsa_circ_129754,RMVar_hsa_circ_129760,RMVar_hsa_circ_98546,RMVar_hsa_circ_126974,RMVar_hsa_circ_129772,RMVar_hsa_circ_129773,RMVar_hsa_circ_85600,RMVar_hsa_circ_89853,RMVar_hsa_circ_19141,RMVar_hsa_circ_288501,RMVar_hsa_circ_129776,RMVar_hsa_circ_351593,RMVar_hsa_circ_129782,RMVar_hsa_circ_129784,RMVar_hsa_circ_285638,RMVar_hsa_circ_323465,RMVar_hsa_circ_350768,RMVar_hsa_circ_129783,RMVar_hsa_circ_315769,RMVar_hsa_circ_30735,RMVar_hsa_circ_129787,RMVar_hsa_circ_91552,RMVar_hsa_circ_303878,RMVar_hsa_circ_315617 63598 RMVar_ID_63598 Human_SNP_ID_5177009 m1A Human chr1 + 19190483 19190483 19190483 CAGTCCAGGCTGTGACCTCTTCCTGAAACTCCAGACTCACATATCCAACTGCCCACTCAACATCT CAGTCCAGGCTGTGACCTCTTCCTGAAACTCCTGACTCACATATCCAACTGCCCACTCAACATCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19190470..19190695 26863196 MeRIP-seq:(Medium) rs1402152600 Functional Loss SNV dbSNP153 33..33 33 - - - 63599 RMVar_ID_63599 Human_SNP_ID_5177051 m1A Human chr1 - 19190678 19190678 19190678 AGGATTTACTGATGGCTTGTATGTTGGGTGTGAAAAAGATGACATCACAATTTTTTGGCTTGAGG AGGATTTACTGATGGCTTGTATGTTGGGTGTGCAAAAGATGACATCACAATTTTTTGGCTTGAGG T G UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19190472..19190960 26863196 MeRIP-seq:(Medium) rs970113781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10711399,Human_RBP_ID_23353449 RMVar_hsa_circ_85305,RMVar_hsa_circ_129658,RMVar_hsa_circ_79086,RMVar_hsa_circ_129659,RMVar_hsa_circ_87791,RMVar_hsa_circ_107674,RMVar_hsa_circ_129676,RMVar_hsa_circ_121451,RMVar_hsa_circ_129677,RMVar_hsa_circ_103221,RMVar_hsa_circ_129683,RMVar_hsa_circ_129682,RMVar_hsa_circ_81223,RMVar_hsa_circ_129687,RMVar_hsa_circ_128134,RMVar_hsa_circ_129689,RMVar_hsa_circ_102082,RMVar_hsa_circ_129692,RMVar_hsa_circ_119603,RMVar_hsa_circ_102844,RMVar_hsa_circ_129698,RMVar_hsa_circ_129699,RMVar_hsa_circ_108770,RMVar_hsa_circ_129702,RMVar_hsa_circ_100435,RMVar_hsa_circ_129710,RMVar_hsa_circ_96918,RMVar_hsa_circ_129714,RMVar_hsa_circ_377953,RMVar_hsa_circ_110459,RMVar_hsa_circ_129728,RMVar_hsa_circ_129729,RMVar_hsa_circ_129751,RMVar_hsa_circ_94494,RMVar_hsa_circ_27446,RMVar_hsa_circ_129755,RMVar_hsa_circ_93158,RMVar_hsa_circ_107229,RMVar_hsa_circ_69721,RMVar_hsa_circ_123901,RMVar_hsa_circ_129754,RMVar_hsa_circ_129760,RMVar_hsa_circ_98546,RMVar_hsa_circ_126974,RMVar_hsa_circ_129772,RMVar_hsa_circ_129773,RMVar_hsa_circ_89853,RMVar_hsa_circ_19141,RMVar_hsa_circ_351593,RMVar_hsa_circ_323465,RMVar_hsa_circ_350768,RMVar_hsa_circ_129783,RMVar_hsa_circ_315769,RMVar_hsa_circ_30735,RMVar_hsa_circ_129787,RMVar_hsa_circ_91552,RMVar_hsa_circ_315617,RMVar_hsa_circ_69723 63600 RMVar_ID_63600 Human_SNP_ID_5181958 m1A Human chr1 - 19210173 19210173 19210173 CGCCGGGGACCCCGGCAACGGGGGCGGACACGACCCCGGGCTGGGAGGTGGCTGTGCGGCCCCTG CGCCGGGGACCCCGGCAACGGGGGCGGACACGGCCCCGGGCTGGGAGGTGGCTGTGCGGCCCCTG T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19210122..19210243 26863196 MeRIP-seq:(Medium) rs756121092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8740100,Human_RBP_ID_9269893,Human_RBP_ID_22426942,Human_RBP_ID_26773335 Human_miRNA_ID_2576917 RMVar_hsa_circ_129795,RMVar_hsa_circ_377104 63601 RMVar_ID_63601 Human_SNP_ID_5182147 m1A Human chr1 + 19210556 19210556 19210556 GGTGGTAGCGACTTGGCTTCCGGGCAGCGGGTAAAGGTGAGTCTGGGGCATGGGTTCAGTGGGCA GGTGGTAGCGACTTGGCTTCCGGGCAGCGGGTTAAGGTGAGTCTGGGGCATGGGTTCAGTGGGCA A T EMC1-AS1 Ensembl:ENSG00000230424 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:19210432..19240290;chr1:19210413..19240290 26863196 MeRIP-seq:(Medium) rs1188446379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5334905,Human_RBP_ID_5541005,Human_RBP_ID_5734261,Human_RBP_ID_18414874,Human_RBP_ID_19034144 Human_Splice_Rec_24941 63602 RMVar_ID_63602 Human_SNP_ID_5192235 m1A Human chr1 + 19251477 19251477 19251477 ACCGCGGCCGCAGGAATCAGCAGCGTAGCCCAAAGCCAGAAACGAGAAGCCCACTCAGCCGCCAT ACCGCGGCCGCAGGAATCAGCAGCGTAGCCCAGAGCCAGAAACGAGAAGCCCACTCAGCCGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19251403..19251501 26863196 MeRIP-seq:(Medium) rs1268800650 Functional Loss SNV dbSNP153 33..33 33 - - - 63603 RMVar_ID_63603 Human_SNP_ID_5192326 m1A Human chr1 + 19251638 19251638 19251638 CCTCGGTCGGACGGGACGCTCGGGATTCAGGGACTGCCTCGGCACACGGGAAGTTGCCCTACAGG CCTCGGTCGGACGGGACGCTCGGGATTCAGGGGCTGCCTCGGCACACGGGAAGTTGCCCTACAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:19251576..19251914;chr1:19251576..19251916 26863196 MeRIP-seq:(Medium) rs978701211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973639,Human_RBP_ID_1251946,Human_RBP_ID_1418014,Human_RBP_ID_5433354,Human_RBP_ID_5485107,Human_RBP_ID_5734443,Human_RBP_ID_8740115,Human_RBP_ID_10712504 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813 63604 RMVar_ID_63604 Human_SNP_ID_5192327 m1A Human chr1 + 19251638 19251638 19251638 CCTCGGTCGGACGGGACGCTCGGGATTCAGGGACTGCCTCGGCACACGGGAAGTTGCCCTACAGG CCTCGGTCGGACGGGACGCTCGGGATTCAGGGTCTGCCTCGGCACACGGGAAGTTGCCCTACAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:19251576..19251914;chr1:19251576..19251916 26863196 MeRIP-seq:(Medium) rs978701211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973639,Human_RBP_ID_1251946,Human_RBP_ID_1418014,Human_RBP_ID_5433354,Human_RBP_ID_5485107,Human_RBP_ID_5734443,Human_RBP_ID_8740115,Human_RBP_ID_10712504 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813 63605 RMVar_ID_63605 Human_SNP_ID_5192328 m1A Human chr1 - 19251640 19251640 19251640 CGCCTGTAGGGCAACTTCCCGTGTGCCGAGGCAGTCCCTGAATCCCGAGCGTCCCGTCCGACCGA CGCCTGTAGGGCAACTTCCCGTGTGCCGAGGCCGTCCCTGAATCCCGAGCGTCCCGTCCGACCGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19251595..19251885 26863196 MeRIP-seq:(Medium) rs141918623 Functional Loss SNV dbSNP153 33..33 33 - - - 63606 RMVar_ID_63606 Human_SNP_ID_5192846 m1A Human chr1 + 19253191 19253191 19253191 AGATGTTGATATTTTGTATAGTGTGGTCGGGAAAGGTCTCACTGATGAAGTGACAAATGAGCAGA AGATGTTGATATTTTGTATAGTGTGGTCGGGAGAGGTCTCACTGATGAAGTGACAAATGAGCAGA A G MRTO4 Ensembl:ENSG00000053372 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19253170..19253412 26863196 MeRIP-seq:(Medium) rs776088977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10712525 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813 63607 RMVar_ID_63607 Human_SNP_ID_5192855 m1A Human chr1 - 19253216 19253216 19253216 GGTTGCTCGCTTCCTTTCTTTATTTTCTGCTCATTTGTCACTTCATCAGTGAGACCTTTCCCGAC GGTTGCTCGCTTCCTTTCTTTATTTTCTGCTCCTTTGTCACTTCATCAGTGAGACCTTTCCCGAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19253203..19253437 26863196 MeRIP-seq:(Medium) rs759047447 Functional Loss SNV dbSNP153 33..33 33 - - - 63608 RMVar_ID_63608 Human_SNP_ID_5202280 m1A Human chr1 + 19287603 19287603 19287603 GCATCAGACTGAGGGCGGCTCCTCCTGCCCCTATACACACATCCTCCCCTCCGGCCACACCTGCC GCATCAGACTGAGGGCGGCTCCTCCTGCCCCTTTACACACATCCTCCCCTCCGGCCACACCTGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19287599..19287697 26863196 MeRIP-seq:(Medium) rs28439369 Functional Loss SNV dbSNP153 33..33 33 - - - 63609 RMVar_ID_63609 Human_SNP_ID_5207149 m1A Human chr1 + 19307088 19307088 19307088 TTCCCGTCCTTGTCCTCATACTTGTACTTGCCAGTCAGCAGGCCCCCTGCGGGAAGGCAGCAATC TTCCCGTCCTTGTCCTCATACTTGTACTTGCCGGTCAGCAGGCCCCCTGCGGGAAGGCAGCAATC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:19307001..19307125 32194978 MeRIP-seq:(Medium) rs765959035 Functional Loss SNV dbSNP153 33..33 33 - - - 63610 RMVar_ID_63610 Human_SNP_ID_5207517 m1A Human chr1 + 19308227 19308226 19308227 CAGAGGGTACAGATCTCGGCCACTTCCCAGCTAGCATAGTTGGAGAGGCCAAGCTCCACGAACTT CAGAGGGTACAGATCTCGGCCACTTCCCAGCT_GCATAGTTGGAGAGGCCAAGCTCCACGAACTT TA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19308176..19308275 32194978 MeRIP-seq:(Medium) rs751138262 Functional Loss DEL dbSNP153 33..33 33 - - - 63611 RMVar_ID_63611 Human_SNP_ID_5207518 m1A Human chr1 + 19308227 19308227 19308227 CAGAGGGTACAGATCTCGGCCACTTCCCAGCTAGCATAGTTGGAGAGGCCAAGCTCCACGAACTT CAGAGGGTACAGATCTCGGCCACTTCCCAGCTGGCATAGTTGGAGAGGCCAAGCTCCACGAACTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19308176..19308275 32194978 MeRIP-seq:(Medium) rs199593810 Functional Loss SNV dbSNP153 33..33 33 - - - 63612 RMVar_ID_63612 Human_SNP_ID_5208576 m1A Human chr1 + 19311946 19311946 19311946 GTTCGGTGTGGCCGCGCTCCAGAAAGGCGCGCACGGCCGCGGCGCTGGCGGGCGCGTCCATGCGG GTTCGGTGTGGCCGCGCTCCAGAAAGGCGCGCGCGGCCGCGGCGCTGGCGGGCGCGTCCATGCGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:19311901..19312075 26863196 MeRIP-seq:(Medium) rs773343655 Functional Loss SNV dbSNP153 33..33 33 - - - 63613 RMVar_ID_63613 Human_SNP_ID_5208606 m1A Human chr1 + 19312007 19312007 19312007 GCGGCGCCCCATCTCCATGGTGCCCAGCACCGAGGCGACCCGCGGTGGCGGTGGCCGGGACATGG GCGGCGCCCCATCTCCATGGTGCCCAGCACCGTGGCGACCCGCGGTGGCGGTGGCCGGGACATGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19311956..19312087 26863196 MeRIP-seq:(Medium) rs1284659516 Functional Loss SNV dbSNP153 33..33 33 - - - 63614 RMVar_ID_63614 Human_SNP_ID_5208634 m1A Human chr1 - 19312054 19312054 19312054 CGTCCACTGCGCGCTTCGCTCTCCGCCGCCCGAGGCCCGCGCGCTCGCCATGTCCCGGCCACCGC CGTCCACTGCGCGCTTCGCTCTCCGCCGCCCGCGGCCCGCGCGCTCGCCATGTCCCGGCCACCGC T G AKR7A2 Ensembl:ENSG00000053371 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:19311901..19312150 26863410 MeRIP-seq:(Medium) rs1342131341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223514,Human_RBP_ID_4072577,Human_RBP_ID_22532053 63615 RMVar_ID_63615 Human_SNP_ID_5208869 m1A Human chr1 - 19312357 19312357 19312357 AAGTTTGCCACCTGCCCCCGGTCCGGCTCACCACGTCCAGATCCGCCGCCAGGGCCCAGCTTCTG AAGTTTGCCACCTGCCCCCGGTCCGGCTCACCCCGTCCAGATCCGCCGCCAGGGCCCAGCTTCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19312325..19312690 26863196 MeRIP-seq:(Medium) rs562851474 Functional Loss SNV dbSNP153 33..33 33 - - - 63616 RMVar_ID_63616 Human_SNP_ID_5216647 m1A Human chr1 + 19338972 19338971 19338973 GGAAGAGCGGAACGGTCGGCGGCACCCCCCCCAGCCCCCACCCCGCGGCCTCCGTGGGACGGGAG GGAAGAGCGGAACGGTCGGCGGCACCCCCCCC__CCCCCACCCCGCGGCCTCCGTGGGACGGGAG CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19338924..19339158 26863196 MeRIP-seq:(Medium) rs1375320897 Functional Loss DEL dbSNP153 33..34 33 - - - 63617 RMVar_ID_63617 Human_SNP_ID_5216648 m1A Human chr1 + 19338972 19338972 19338972 GGAAGAGCGGAACGGTCGGCGGCACCCCCCCCAGCCCCCACCCCGCGGCCTCCGTGGGACGGGAG GGAAGAGCGGAACGGTCGGCGGCACCCCCCCCCGCCCCCACCCCGCGGCCTCCGTGGGACGGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19338924..19339158 26863196 MeRIP-seq:(Medium) rs913518335 Functional Loss SNV dbSNP153 33..33 33 - - - 63618 RMVar_ID_63618 Human_SNP_ID_5216816 m1A Human chr1 + 19339407 19339407 19339407 TATTCTCAGGGAGAGATGGCGCTGTGCGGTCAATGATGCAGCTGTTATGTGACCTGTCGGGGAGG TATTCTCAGGGAGAGATGGCGCTGTGCGGTCAGTGATGCAGCTGTTATGTGACCTGTCGGGGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:19339218..19339560;chr1:19339126..19339531 26863196 MeRIP-seq:(Medium) rs964293204 Functional Loss SNV dbSNP153 33..33 33 - - - 63619 RMVar_ID_63619 Human_SNP_ID_5227131 m1A Human chr1 - 19378589 19378589 19378589 TGGAGGATGGGGCCATGCCGTCAGCTCGGCTGAGAAAGCTGGAGGTGGAAGCCAACAATGCCTTT TGGAGGATGGGGCCATGCCGTCAGCTCGGCTGCGAAAGCTGGAGGTGGAAGCCAACAATGCCTTT T G CAPZB Ensembl:ENSG00000077549 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:19378526..19420025 32194978 MeRIP-seq:(Medium) rs1042802256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_336877,Human_RBP_ID_973676,Human_RBP_ID_5234509,Human_RBP_ID_22426952,Human_RBP_ID_26849329 Human_Splice_Rec_25324,Human_Splice_Rec_25325,Human_Splice_Rec_25342,Human_Splice_Rec_25343,Human_Splice_Rec_25356,Human_Splice_Rec_25357,Human_Splice_Rec_25380,Human_Splice_Rec_25381,Human_Splice_Rec_25396,Human_Splice_Rec_25397,Human_Splice_Rec_25410,Human_Splice_Rec_25411,Human_Splice_Rec_25426,Human_Splice_Rec_25427,Human_Splice_Rec_25440,Human_Splice_Rec_25441,Human_Splice_Rec_25456,Human_Splice_Rec_25457,Human_Splice_Rec_25468,Human_Splice_Rec_25469,Human_Splice_Rec_25480,Human_Splice_Rec_25481,Human_Splice_Rec_25488,Human_Splice_Rec_25489,Human_Splice_Rec_25498,Human_Splice_Rec_25499,Human_Splice_Rec_25502 Human_miRNA_ID_2014491 RMVar_hsa_circ_5926,RMVar_hsa_circ_61484,RMVar_hsa_circ_265503,RMVar_hsa_circ_72794,RMVar_hsa_circ_330593,RMVar_hsa_circ_91800,RMVar_hsa_circ_275937,RMVar_hsa_circ_129828,RMVar_hsa_circ_310208,RMVar_hsa_circ_129829 63620 RMVar_ID_63620 Human_SNP_ID_5228472 m1A Human chr1 - 19383769 19383769 19383769 AGGAGCAGGCATAGGGACACTTTAAGCTTGAGAGGCCCATTAGATCAAAGTGGAGATACCAGGTA AGGAGCAGGCATAGGGACACTTTAAGCTTGAGGGGCCCATTAGATCAAAGTGGAGATACCAGGTA T C CAPZB Ensembl:ENSG00000077549 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19383764..19383938 26863196 MeRIP-seq:(Medium) rs1022946597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5926,RMVar_hsa_circ_61484,RMVar_hsa_circ_72794,RMVar_hsa_circ_330593,RMVar_hsa_circ_91800,RMVar_hsa_circ_275937,RMVar_hsa_circ_129828,RMVar_hsa_circ_310208,RMVar_hsa_circ_129829 63621 RMVar_ID_63621 Human_SNP_ID_5245934 m1A Human chr1 + 19452070 19452070 19452070 GCCCCAACCCATCCTCTCTGCACATCTGGGTCAGGGCAAGCTTTCCAAGACTTACCTGGCCAGTC GCCCCAACCCATCCTCTCTGCACATCTGGGTCGGGGCAAGCTTTCCAAGACTTACCTGGCCAGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19452068..19452323 26863196 MeRIP-seq:(Medium) rs1234518002 Functional Loss SNV dbSNP153 33..33 33 - - - 63622 RMVar_ID_63622 Human_SNP_ID_5245940 m1A Human chr1 + 19452099 19452099 19452099 GTCAGGGCAAGCTTTCCAAGACTTACCTGGCCAGTCCTCACTGCCCACCCCCTGCAGTCCTCTTA GTCAGGGCAAGCTTTCCAAGACTTACCTGGCCGGTCCTCACTGCCCACCCCCTGCAGTCCTCTTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19452094..19452186 26863196 MeRIP-seq:(Medium) rs956619946 Functional Loss SNV dbSNP153 33..33 33 - - - 63623 RMVar_ID_63623 Human_SNP_ID_5246364 m1A Human chr1 - 19453570 19453570 19453570 GTACAAGGCTTCCCAGGTTGAGACATAGAAAGAGGCGCTGGTGGCCAGGGGCAGTGGCTCACGCC GTACAAGGCTTCCCAGGTTGAGACATAGAAAGTGGCGCTGGTGGCCAGGGGCAGTGGCTCACGCC T A CAPZB Ensembl:ENSG00000077549 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:19453567..19453704;chr1:19453567..19453669 26863196 MeRIP-seq:(Medium) rs891689216 Functional Loss SNV dbSNP153 33..33 33 - - - 63624 RMVar_ID_63624 Human_SNP_ID_5250271 m1A Human chr1 + 19468755 19468755 19468755 TCCTCTGAGTTTAAATTAGTCATTTCCCCAGCACCCGCCATGCCCTCCTGGGCCACTGAGTCGGC TCCTCTGAGTTTAAATTAGTCATTTCCCCAGCCCCCGCCATGCCCTCCTGGGCCACTGAGTCGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19468752..19468872 26863196 MeRIP-seq:(Medium) rs1414472623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129832 63625 RMVar_ID_63625 Human_SNP_ID_5282890 m1A Human chr1 - 19597051 19597051 19597051 CACCGGTCCCACTTCCTGCCGAGCTCCGACTCAGACATGTTCCCCACCCGCGCCTCCAGCTTTCC CACCGGTCCCACTTCCTGCCGAGCTCCGACTCCGACATGTTCCCCACCCGCGCCTCCAGCTTTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:19596959..19597850;chr1:19596976..19600890;chr1:19596951..19597185;chr1:19597001..19597167 26863196 MeRIP-seq:(Medium) rs772196548 Functional Loss SNV dbSNP153 33..33 33 - - - 63626 RMVar_ID_63626 Human_SNP_ID_5282906 m1A Human chr1 + 19597067 19597067 19597067 GGGTGGGGAACATGTCTGAGTCGGAGCTCGGCAGGAAGTGGGACCGGTGTCTGGCGGATGCGGTC GGGTGGGGAACATGTCTGAGTCGGAGCTCGGCGGGAAGTGGGACCGGTGTCTGGCGGATGCGGTC A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding 5'UTR,CDS,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr1:19597016..19597136;chr1:19597026..19597850 26863196,26863410 MeRIP-seq:(Medium) rs748809535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224290,Human_RBP_ID_337252,Human_RBP_ID_745250,Human_RBP_ID_1418317,Human_RBP_ID_4015796,Human_RBP_ID_5109012,Human_RBP_ID_5311559,Human_RBP_ID_9318655,Human_RBP_ID_10718874,Human_RBP_ID_17647380,Human_RBP_ID_18414876,Human_RBP_ID_22430258,Human_RBP_ID_22871187,Human_RBP_ID_23121957,Human_RBP_ID_23354777,Human_RBP_ID_26849575 Human_Splice_Rec_25509,Human_Splice_Rec_25513,Human_Splice_Rec_25519,Human_Splice_Rec_25525,Human_Splice_Rec_25527,Human_Splice_Rec_25533,Human_Splice_Rec_25541,Human_Splice_Rec_25549,Human_Splice_Rec_25557,Human_Splice_Rec_25559,Human_Splice_Rec_25569,Human_Splice_Rec_25651,Human_Splice_Rec_25669,Human_Splice_Rec_25685 63627 RMVar_ID_63627 Human_SNP_ID_5282995 m1A Human chr1 + 19597308 19597308 19597308 GGGCGGCGGGCACAGACCCGAGGAGCCGGAGCAGCAGCCCGGGTGCGGGGTGGAGTTGCAGCCCG GGGCGGCGGGCACAGACCCGAGGAGCCGGAGCGGCAGCCCGGGTGCGGGGTGGAGTTGCAGCCCG A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19597303..19597406 26863196 MeRIP-seq:(Medium) rs943709589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5334925,Human_RBP_ID_18455524,Human_RBP_ID_18928053 63628 RMVar_ID_63628 Human_SNP_ID_5288905 m1A Human chr1 - 19622046 19622046 19622046 ATGCTAAATCTCATAGCAGTAACTTCACAAAGATAACATTAACATTTCTTAAATGTGAACATCAT ATGCTAAATCTCATAGCAGTAACTTCACAAAGTTAACATTAACATTTCTTAAATGTGAACATCAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19622043..19622150 26863196 MeRIP-seq:(Medium) rs1034508725 Functional Loss SNV dbSNP153 33..33 33 - - - 63629 RMVar_ID_63629 Human_SNP_ID_5297352 m1A Human chr1 - 19655062 19655062 19655062 TGGGTGGTGGGGCAGCCAGTAGCATGGCAGGGAGGACAGCCCCCACCAGGACCCGAAGCATCATG TGGGTGGTGGGGCAGCCAGTAGCATGGCAGGGGGGACAGCCCCCACCAGGACCCGAAGCATCATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19655001..19655225 26863196 MeRIP-seq:(Medium) rs770313889 Functional Loss SNV dbSNP153 33..33 33 - - - 63630 RMVar_ID_63630 Human_SNP_ID_5297863 m1A Human chr1 + 19656933 19656933 19656933 CAGGGTGGACAAGCTGGTGGAGAAGATCCTGCACTGTAGCTGCCAGGCCTGCGGCAAGGAGCCTA CAGGGTGGACAAGCTGGTGGAGAAGATCCTGCCCTGTAGCTGCCAGGCCTGCGGCAAGGAGCCTA A C NBL1 Ensembl:ENSG00000158747 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19656851..19657000 26863196 MeRIP-seq:(Medium) rs778522323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_25574,Human_Splice_Rec_25580,Human_Splice_Rec_25586,Human_Splice_Rec_25592,Human_Splice_Rec_25598,Human_Splice_Rec_25604,Human_Splice_Rec_25610,Human_Splice_Rec_25616,Human_Splice_Rec_25622,Human_Splice_Rec_25628,Human_Splice_Rec_25638,Human_Splice_Rec_25644,Human_Splice_Rec_25650,Human_Splice_Rec_25668,Human_Splice_Rec_25684,Human_Splice_Rec_25692 Human_miRNA_ID_2053186,Human_miRNA_ID_2077385,Human_miRNA_ID_2079711,Human_miRNA_ID_2090251 RMVar_hsa_circ_103499,RMVar_hsa_circ_129834 63631 RMVar_ID_63631 Human_SNP_ID_5297864 m1A Human chr1 + 19656933 19656933 19656933 CAGGGTGGACAAGCTGGTGGAGAAGATCCTGCACTGTAGCTGCCAGGCCTGCGGCAAGGAGCCTA CAGGGTGGACAAGCTGGTGGAGAAGATCCTGCGCTGTAGCTGCCAGGCCTGCGGCAAGGAGCCTA A G NBL1 Ensembl:ENSG00000158747 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19656851..19657000 26863196 MeRIP-seq:(Medium) rs778522323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_25574,Human_Splice_Rec_25580,Human_Splice_Rec_25586,Human_Splice_Rec_25592,Human_Splice_Rec_25598,Human_Splice_Rec_25604,Human_Splice_Rec_25610,Human_Splice_Rec_25616,Human_Splice_Rec_25622,Human_Splice_Rec_25628,Human_Splice_Rec_25638,Human_Splice_Rec_25644,Human_Splice_Rec_25650,Human_Splice_Rec_25668,Human_Splice_Rec_25684,Human_Splice_Rec_25692 Human_miRNA_ID_2053186,Human_miRNA_ID_2077385,Human_miRNA_ID_2079711,Human_miRNA_ID_2090251 RMVar_hsa_circ_103499,RMVar_hsa_circ_129834 63632 RMVar_ID_63632 Human_SNP_ID_5298198 m1A Human chr1 + 19657856 19657856 19657856 AGGAAAGGGAAGAGTCTTCCAAGGCCAGAAGGAGGGGGACAACCCCCCAAGACCATCCCTGAAGA AGGAAAGGGAAGAGTCTTCCAAGGCCAGAAGGCGGGGGACAACCCCCCAAGACCATCCCTGAAGA A C NBL1 Ensembl:ENSG00000158747 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19657806..19658189 26863196 MeRIP-seq:(Medium) rs1192646268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103499,RMVar_hsa_circ_129834 63633 RMVar_ID_63633 Human_SNP_ID_5323623 m1A Human chr1 - 19759195 19759195 19759195 TGTCAGCATCAGCTGTTGGGTTACATGTCGGGACAGGGAAACAAGAACTAAGAGCAATGCCCAGG TGTCAGCATCAGCTGTTGGGTTACATGTCGGGGCAGGGAAACAAGAACTAAGAGCAATGCCCAGG T C TMCO4 Ensembl:ENSG00000162542 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19759190..19759586 26863196 MeRIP-seq:(Medium) rs553156935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327,RMVar_hsa_circ_97610,RMVar_hsa_circ_129836,RMVar_hsa_circ_13081,RMVar_hsa_circ_42492,RMVar_hsa_circ_306610,RMVar_hsa_circ_55796,RMVar_hsa_circ_129837,RMVar_hsa_circ_71772,RMVar_hsa_circ_52963,RMVar_hsa_circ_44720,RMVar_hsa_circ_65127,RMVar_hsa_circ_337752,RMVar_hsa_circ_129840,RMVar_hsa_circ_36642 63634 RMVar_ID_63634 Human_SNP_ID_5323642 m1A Human chr1 - 19759272 19759269 19759272 CGAGGGCTGTGGCTGTGGCGGTGGCAGTGGAGAAGGAGTGAAGTGGTCAAACCCAGGATATGTTT CGAGGGCTGTGGCTGTGGCGGTGGCAGTGGAG___GAGTGAAGTGGTCAAACCCAGGATATGTTT CCTT C TMCO4 Ensembl:ENSG00000162542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19759243..19759375 26863196 MeRIP-seq:(Medium) rs1396686760 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_327,RMVar_hsa_circ_97610,RMVar_hsa_circ_129836,RMVar_hsa_circ_13081,RMVar_hsa_circ_42492,RMVar_hsa_circ_306610,RMVar_hsa_circ_55796,RMVar_hsa_circ_129837,RMVar_hsa_circ_71772,RMVar_hsa_circ_52963,RMVar_hsa_circ_44720,RMVar_hsa_circ_65127,RMVar_hsa_circ_337752,RMVar_hsa_circ_129840,RMVar_hsa_circ_36642 63635 RMVar_ID_63635 Human_SNP_ID_5323643 m1A Human chr1 - 19759272 19759272 19759272 CGAGGGCTGTGGCTGTGGCGGTGGCAGTGGAGAAGGAGTGAAGTGGTCAAACCCAGGATATGTTT CGAGGGCTGTGGCTGTGGCGGTGGCAGTGGAGGAGGAGTGAAGTGGTCAAACCCAGGATATGTTT T C TMCO4 Ensembl:ENSG00000162542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19759243..19759375 26863196 MeRIP-seq:(Medium) rs1395124987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327,RMVar_hsa_circ_97610,RMVar_hsa_circ_129836,RMVar_hsa_circ_13081,RMVar_hsa_circ_42492,RMVar_hsa_circ_306610,RMVar_hsa_circ_55796,RMVar_hsa_circ_129837,RMVar_hsa_circ_71772,RMVar_hsa_circ_52963,RMVar_hsa_circ_44720,RMVar_hsa_circ_65127,RMVar_hsa_circ_337752,RMVar_hsa_circ_129840,RMVar_hsa_circ_36642 63636 RMVar_ID_63636 Human_SNP_ID_5361870 m1A Human chr1 + 19911973 19911973 19911973 TCTGACCTATGTCTTTGAAGCAGCTGCTTTGTAGAGTCCCTCTCTTTACTGTCCTCGTTAGGACT TCTGACCTATGTCTTTGAAGCAGCTGCTTTGTGGAGTCCCTCTCTTTACTGTCCTCGTTAGGACT A G OTUD3 Ensembl:ENSG00000169914 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17401847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337902,Human_RBP_ID_5739855,Human_RBP_ID_10728156 Human_miRNA_ID_1624678,Human_miRNA_ID_1665175,Human_miRNA_ID_2351033,Human_miRNA_ID_2836857,Human_miRNA_ID_2854733,Human_miRNA_ID_2883855,Human_miRNA_ID_3046579 GWAS_ID_7727,GWAS_ID_7728,GWAS_ID_7729,GWAS_ID_7730 RMVar_hsa_circ_378564,RMVar_hsa_circ_129849,RMVar_hsa_circ_266267 63637 RMVar_ID_63637 Human_SNP_ID_5367316 m1A Human chr1 - 19932910 19932898 19932910 GTGATGGTGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGT GTGATGGTGATTATAATGATGGTGATGGTGAT____________GATGACAGTGATGTTGATGGT CACCATCATCATT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19932861..19932929 26863196 MeRIP-seq:(Medium) rs1451728096 Functional Loss DEL dbSNP153 33..44 33 - - - 63638 RMVar_ID_63638 Human_SNP_ID_5367323 m1A Human chr1 - 19932903 19932903 19932903 TGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGTGATGATA TGATTATAATGATGGTGATGGTGATAATGATGGTGGTGATGACAGTGATGTTGATGGTGATGATA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:19932820..19932958 26863196 MeRIP-seq:(Medium) rs113316862 Functional Loss SNV dbSNP153 33..33 33 - - - 63639 RMVar_ID_63639 Human_SNP_ID_5367327 m1A Human chr1 - 19932910 19932907 19932910 GTGATGGTGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGT GTGATGGTGATTATAATGATGGTGATGGTGAT___GATGATGGTGATGACAGTGATGTTGATGGT CATT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19932861..19932929 26863196 MeRIP-seq:(Medium) rs1197449809 Functional Loss DEL dbSNP153 33..35 33 - - - 63640 RMVar_ID_63640 Human_SNP_ID_5367333 m1A Human chr1 - 19932910 19932910 19932911 GTGATGGTGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGT GTGATGGTGATTATAATGATGGTGATGGTGAAGATGATGATGGTGATGACAGTGATGTTGATGGT TA CT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19932861..19932929 26863196 MeRIP-seq:(Medium) rs796820956 Functional Loss MNV dbSNP153 32..33 33 - - - 63641 RMVar_ID_63641 Human_SNP_ID_5367334 m1A Human chr1 - 19932910 19932910 19932910 GTGATGGTGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGT GTGATGGTGATTATAATGATGGTGATGGTGATTATGATGATGGTGATGACAGTGATGTTGATGGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19932861..19932929 26863196 MeRIP-seq:(Medium) rs372136730 Functional Loss SNV dbSNP153 33..33 33 - - - 63642 RMVar_ID_63642 Human_SNP_ID_5367335 m1A Human chr1 - 19932910 19932910 19932910 GTGATGGTGATTATAATGATGGTGATGGTGATAATGATGATGGTGATGACAGTGATGTTGATGGT GTGATGGTGATTATAATGATGGTGATGGTGATGATGATGATGGTGATGACAGTGATGTTGATGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19932861..19932929 26863196 MeRIP-seq:(Medium) rs372136730 Functional Loss SNV dbSNP153 33..33 33 - - - 63643 RMVar_ID_63643 Human_SNP_ID_5504348 m1A Human chr1 + 20485345 20485345 20485345 GGCCCACGTCGCCGCCGTCGCCGTAGGGGCTCAGCTTCTCGTCGCCGTAGGGCAGCACCTCCGAC GGCCCACGTCGCCGCCGTCGCCGTAGGGGCTCGGCTTCTCGTCGCCGTAGGGCAGCACCTCCGAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:20485301..20485431 26863196 MeRIP-seq:(Medium) rs1199048111 Functional Loss SNV dbSNP153 33..33 33 - - - 63644 RMVar_ID_63644 Human_SNP_ID_5504413 m1A Human chr1 - 20485553 20485553 20485553 CAGCCGCGGGCGCTCTCCGGGCCGCTCGCGCGAGTGCCGCGCTCTTGCCCTAGCGGCGTCCCCCG CAGCCGCGGGCGCTCTCCGGGCCGCTCGCGCGCGTGCCGCGCTCTTGCCCTAGCGGCGTCCCCCG T G CAMK2N1 Ensembl:ENSG00000162545 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:20485506..20485629 26863196 MeRIP-seq:(Medium) rs1047946337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075231 RMVar_hsa_circ_108645,RMVar_hsa_circ_129853 63645 RMVar_ID_63645 Human_SNP_ID_5504464 m1A Human chr1 - 20485726 20485699 20485726 GCCCTCCTCGGTCCCGCGCCCTCCGGGCTCGCAGGGACGTCTCCTCCCTCCCGGCTCGCGGCCCC GCCCTCCTCGGTCCCGCGCCCTCCGGGCTCGC___________________________GGCCCC CGCGAGCCGGGAGGGAGGAGACGTCCCT C CAMK2N1 Ensembl:ENSG00000162545 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20485677..20486258 26863196 MeRIP-seq:(Medium) rs1015754733 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_3330064,Human_RBP_ID_5125642 RMVar_hsa_circ_108645,RMVar_hsa_circ_129853 63646 RMVar_ID_63646 Human_SNP_ID_5504478 m1A Human chr1 + 20485751 20485751 20485751 ACGTCCCTGCGAGCCCGGAGGGCGCGGGACCGAGGAGGGCGCACCCCGGGAGCCGGGCGGGCCGG ACGTCCCTGCGAGCCCGGAGGGCGCGGGACCGGGGAGGGCGCACCCCGGGAGCCGGGCGGGCCGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:20485479..20485825 26863410 MeRIP-seq:(Medium) rs1295940691 Functional Loss SNV dbSNP153 33..33 33 - - - 63647 RMVar_ID_63647 Human_SNP_ID_5529994 m1A Human chr1 - 20589144 20589144 20589144 TGGACACACTCAGGCTTCAGGGTGCAGGCAGGACGCTTCTGGGCCATGTTGGTACCCCGGGCAGG TGGACACACTCAGGCTTCAGGGTGCAGGCAGGGCGCTTCTGGGCCATGTTGGTACCCCGGGCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20588972..20589223 26863196 MeRIP-seq:(Medium) rs1214227643 Functional Loss SNV dbSNP153 33..33 33 - - - 63648 RMVar_ID_63648 Human_SNP_ID_5537191 m1A Human chr1 - 20618746 20618745 20618747 GGAAAGGTGGGGCAGGGGGCGGCGGTGTTCTAAGTCCCAAGGCAGGTTGCTAGGAGGGGTGCTGA GGAAAGGTGGGGCAGGGGGCGGCGGTGTTCT__GTCCCAAGGCAGGTTGCTAGGAGGGGTGCTGA CTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20618494..20618832 26863196 MeRIP-seq:(Medium) rs1002900280 Functional Loss DEL dbSNP153 32..33 33 - - - 63649 RMVar_ID_63649 Human_SNP_ID_5540937 m1A Human chr1 - 20633521 20633512 20633521 GCCATGGTGGCGCCGCGGCCCGGTGCCCCCGCAGCCGCCGCTGCCGCCACCACCGGCGTCCCCCG GCCATGGTGGCGCCGCGGCCCGGTGCCCCCGC_________TGCCGCCACCACCGGCGTCCCCCG AGCGGCGGCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:20633476..20633950;chr1:20633476..20633979;chr1:20633451..20633969 26863196 MeRIP-seq:(Medium) rs1553145472 Functional Loss DEL dbSNP153 33..41 33 - - - 63650 RMVar_ID_63650 Human_SNP_ID_5540943 m1A Human chr1 - 20633521 20633521 20633521 GCCATGGTGGCGCCGCGGCCCGGTGCCCCCGCAGCCGCCGCTGCCGCCACCACCGGCGTCCCCCG GCCATGGTGGCGCCGCGGCCCGGTGCCCCCGCTGCCGCCGCTGCCGCCACCACCGGCGTCCCCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:20633476..20633950;chr1:20633476..20633979;chr1:20633451..20633969 26863196 MeRIP-seq:(Medium) rs1489837466 Functional Loss SNV dbSNP153 33..33 33 - - - 63651 RMVar_ID_63651 Human_SNP_ID_5542153 m1A Human chr1 + 20637928 20637928 20637928 TTGCAGGGCTTTCGGCTGGAGGAGTATCTGATAGGGCAGTCCATTGGTAAGGGCTGCAGTGCTGC TTGCAGGGCTTTCGGCTGGAGGAGTATCTGATGGGGCAGTCCATTGGTAAGGGCTGCAGTGCTGC A G PINK1 Ensembl:ENSG00000158828 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:20637812..20638165;chr1:20637826..20638152 26863196 MeRIP-seq:(Medium) rs374204111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1252452,Human_RBP_ID_4020662,Human_RBP_ID_8741965,Human_RBP_ID_8962048,Human_RBP_ID_17736937,Human_RBP_ID_18561204 Human_Splice_Rec_26406 RMVar_hsa_circ_129856,RMVar_hsa_circ_305643 63652 RMVar_ID_63652 Human_SNP_ID_5544203 m1A Human chr1 + 20645679 20645677 20645679 CGTGGACCATCTGGTTCAACAGGGCATCGCGCACAGAGACCTGAAATCCGACAACATCCTTGTGG CGTGGACCATCTGGTTCAACAGGGCATCGCG__CAGAGACCTGAAATCCGACAACATCCTTGTGG GCA G PINK1 Ensembl:ENSG00000158828 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20645515..20645758 26863196 MeRIP-seq:(Medium) rs764252130 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_26413,Human_Splice_Rec_26423,Human_Splice_Rec_26427 RMVar_hsa_circ_19499,RMVar_hsa_circ_364179,RMVar_hsa_circ_353812,RMVar_hsa_circ_129859 63653 RMVar_ID_63653 Human_SNP_ID_5544204 m1A Human chr1 + 20645679 20645679 20645679 CGTGGACCATCTGGTTCAACAGGGCATCGCGCACAGAGACCTGAAATCCGACAACATCCTTGTGG CGTGGACCATCTGGTTCAACAGGGCATCGCGCGCAGAGACCTGAAATCCGACAACATCCTTGTGG A G PINK1 Ensembl:ENSG00000158828 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20645515..20645758 26863196 MeRIP-seq:(Medium) rs1553146578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_26413,Human_Splice_Rec_26423,Human_Splice_Rec_26427 RMVar_hsa_circ_19499,RMVar_hsa_circ_364179,RMVar_hsa_circ_353812,RMVar_hsa_circ_129859 63654 RMVar_ID_63654 Human_SNP_ID_5545811 m1A Human chr1 + 20650794 20650792 20650794 GTGAGGGTGGGAGTCAGGAGACAAGACAGCGCAGAGAGGGCTGGTTAGCCGGAAAAGGCCTCGGG GTGAGGGTGGGAGTCAGGAGACAAGACAGCG__GAGAGGGCTGGTTAGCCGGAAAAGGCCTCGGG GCA G PINK1 Ensembl:ENSG00000158828 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:20650651..20650947;chr1:20650495..20651067;chr1:20650647..20650955 26863196 MeRIP-seq:(Medium) rs1338122151 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_224306,Human_RBP_ID_339818,Human_RBP_ID_745270,Human_RBP_ID_23204982 63655 RMVar_ID_63655 Human_SNP_ID_5545812 m1A Human chr1 + 20650794 20650793 20650795 GTGAGGGTGGGAGTCAGGAGACAAGACAGCGCAGAGAGGGCTGGTTAGCCGGAAAAGGCCTCGGG GTGAGGGTGGGAGTCAGGAGACAAGACAGCGC__AGAGGGCTGGTTAGCCGGAAAAGGCCTCGGG CAG C PINK1 Ensembl:ENSG00000158828 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:20650651..20650947;chr1:20650495..20651067;chr1:20650647..20650955 26863196 MeRIP-seq:(Medium) rs1374353379 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_224306,Human_RBP_ID_339818,Human_RBP_ID_745270,Human_RBP_ID_23204982 63656 RMVar_ID_63656 Human_SNP_ID_5546277 m1A Human chr1 - 20651964 20651964 20651964 AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C PINK1-AS,DDOST Ensembl:ENSG00000117242,Ensembl:ENSG00000244038 lincRNA,Protein coding exon,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1131982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339840,Human_RBP_ID_5109015,Human_RBP_ID_5136109 63657 RMVar_ID_63657 Human_SNP_ID_5546383 m1A Human chr1 + 20652328 20652328 20652328 AAACAAAGCAAAACAAAACCACCAATCCTAATAACCCCCCTCCTTGCCCCGTCTCCACGCTGTGC AAACAAAGCAAAACAAAACCACCAATCCTAATCACCCCCCTCCTTGCCCCGTCTCCACGCTGTGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:20652226..20652500 32194978 MeRIP-seq:(Medium) rs1159272239 Functional Loss SNV dbSNP153 33..33 33 - - - 63658 RMVar_ID_63658 Human_SNP_ID_5546398 m1A Human chr1 - 20652339 20652339 20652339 GAGCCCTCTCCGCACAGCGTGGAGACGGGGCAAGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT GAGCCCTCTCCGCACAGCGTGGAGACGGGGCAGGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT T C DDOST Ensembl:ENSG00000244038 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746815,Human_RBP_ID_5746271,Human_RBP_ID_9352482,Human_RBP_ID_17646103,Human_RBP_ID_26375074 Clinvar_Rec_233,Clinvar_Rec_234,Clinvar_Rec_235,Clinvar_Rec_236 GWAS_ID_7731,GWAS_ID_7732,GWAS_ID_7733,GWAS_ID_7734,GWAS_ID_7735,GWAS_ID_7736,GWAS_ID_7737,GWAS_ID_7738,GWAS_ID_7739,GWAS_ID_7740,GWAS_ID_7741,GWAS_ID_7742,GWAS_ID_7743,GWAS_ID_7744,GWAS_ID_7745,GWAS_ID_7746,GWAS_ID_7747,GWAS_ID_7748,GWAS_ID_7749 63659 RMVar_ID_63659 Human_SNP_ID_5546399 m1A Human chr1 - 20652339 20652339 20652339 GAGCCCTCTCCGCACAGCGTGGAGACGGGGCAAGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT GAGCCCTCTCCGCACAGCGTGGAGACGGGGCACGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT T G DDOST Ensembl:ENSG00000244038 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746815,Human_RBP_ID_5746271,Human_RBP_ID_9352482,Human_RBP_ID_17646103,Human_RBP_ID_26375074 Clinvar_Rec_233,Clinvar_Rec_234,Clinvar_Rec_235,Clinvar_Rec_236 GWAS_ID_7731,GWAS_ID_7732,GWAS_ID_7733,GWAS_ID_7734,GWAS_ID_7735,GWAS_ID_7736,GWAS_ID_7737,GWAS_ID_7738,GWAS_ID_7739,GWAS_ID_7740,GWAS_ID_7741,GWAS_ID_7742,GWAS_ID_7743,GWAS_ID_7744,GWAS_ID_7745,GWAS_ID_7746,GWAS_ID_7747,GWAS_ID_7748,GWAS_ID_7749 63660 RMVar_ID_63660 Human_SNP_ID_5546631 m1A Human chr1 - 20652970 20652970 20652970 CAGCCCTGGCTAACCTGGCCTTTTATCTCAGGAGTATAGCATCGTGATCCAGCAGCTCTCAAATG CAGCCCTGGCTAACCTGGCCTTTTATCTCAGGGGTATAGCATCGTGATCCAGCAGCTCTCAAATG T C DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:20652926..20652975 32194978 MeRIP-seq:(Medium) rs1196981268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17762394,Human_RBP_ID_22633034,Human_RBP_ID_22748910 Human_Splice_Rec_26452,Human_Splice_Rec_26472,Human_Splice_Rec_26492 RMVar_hsa_circ_129861,RMVar_hsa_circ_32594,RMVar_hsa_circ_85267,RMVar_hsa_circ_331058,RMVar_hsa_circ_129860,RMVar_hsa_circ_108360,RMVar_hsa_circ_129862 63661 RMVar_ID_63661 Human_SNP_ID_5547027 m1A Human chr1 - 20654302 20654299 20654302 CTGGGCTCCAGGCCAGGAACAATGCCCGCGTCATCTTCAGCGGCTCCCTCGACTTCTTCAGCGAC CTGGGCTCCAGGCCAGGAACAATGCCCGCGTC___TTCAGCGGCTCCCTCGACTTCTTCAGCGAC AGAT A DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20654252..20654370 26863196 MeRIP-seq:(Medium) rs1272297547 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_339869,Human_RBP_ID_1252456,Human_RBP_ID_4020804,Human_RBP_ID_17215309,Human_RBP_ID_17736986,Human_RBP_ID_18186893,Human_RBP_ID_18429364 Human_Splice_Rec_26448,Human_Splice_Rec_26449,Human_Splice_Rec_26468,Human_Splice_Rec_26469,Human_Splice_Rec_26488,Human_Splice_Rec_26489 RMVar_hsa_circ_50148,RMVar_hsa_circ_85267,RMVar_hsa_circ_331058,RMVar_hsa_circ_129860,RMVar_hsa_circ_91376,RMVar_hsa_circ_108360,RMVar_hsa_circ_129862,RMVar_hsa_circ_129863,RMVar_hsa_circ_42250,RMVar_hsa_circ_328544,RMVar_hsa_circ_375569,RMVar_hsa_circ_129864 63662 RMVar_ID_63662 Human_SNP_ID_5547593 m1A Human chr1 + 20655750 20655750 20655750 AGCCGTTTTCTCCTCGTCAAACTCAATCCCGCACTCACTGCCCAGCTCTCGAAGAGGGTCACCTG AGCCGTTTTCTCCTCGTCAAACTCAATCCCGCCCTCACTGCCCAGCTCTCGAAGAGGGTCACCTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:20654306..20655800 32194978 MeRIP-seq:(Medium) rs768942021 Functional Loss SNV dbSNP153 33..33 33 - - - 63663 RMVar_ID_63663 Human_SNP_ID_5547594 m1A Human chr1 + 20655754 20655754 20655754 GTTTTCTCCTCGTCAAACTCAATCCCGCACTCACTGCCCAGCTCTCGAAGAGGGTCACCTGCACA GTTTTCTCCTCGTCAAACTCAATCCCGCACTCGCTGCCCAGCTCTCGAAGAGGGTCACCTGCACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20655704..20655814 26863196 MeRIP-seq:(Medium) rs776997435 Functional Loss SNV dbSNP153 33..33 33 - - - 63664 RMVar_ID_63664 Human_SNP_ID_5549078 m1A Human chr1 - 20661338 20661338 20661338 CCTTCGGCAGGAGGAGGAAGATGGAGCCCAGCACCGCGGCCCGGGCTTGGGCCCTCTTTTGGTTG CCTTCGGCAGGAGGAGGAAGATGGAGCCCAGCCCCGCGGCCCGGGCTTGGGCCCTCTTTTGGTTG T G DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20661226..20661455 26863196 MeRIP-seq:(Medium) rs749137941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1128,Human_RBP_ID_224844,Human_RBP_ID_339885,Human_RBP_ID_745898,Human_RBP_ID_4020830,Human_RBP_ID_22428188,Human_RBP_ID_23122086,Human_RBP_ID_26851368 63665 RMVar_ID_63665 Human_SNP_ID_5549080 m1A Human chr1 - 20661341 20661341 20661341 GGTCCTTCGGCAGGAGGAGGAAGATGGAGCCCAGCACCGCGGCCCGGGCTTGGGCCCTCTTTTGG GGTCCTTCGGCAGGAGGAGGAAGATGGAGCCCGGCACCGCGGCCCGGGCTTGGGCCCTCTTTTGG T C DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:20661235..20661400 26863196 MeRIP-seq:(Medium) rs1166127455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1128,Human_RBP_ID_224844,Human_RBP_ID_339885,Human_RBP_ID_745898,Human_RBP_ID_4020830,Human_RBP_ID_22428188,Human_RBP_ID_23122086,Human_RBP_ID_26851368 63666 RMVar_ID_63666 Human_SNP_ID_5549081 m1A Human chr1 - 20661341 20661341 20661341 GGTCCTTCGGCAGGAGGAGGAAGATGGAGCCCAGCACCGCGGCCCGGGCTTGGGCCCTCTTTTGG GGTCCTTCGGCAGGAGGAGGAAGATGGAGCCCCGCACCGCGGCCCGGGCTTGGGCCCTCTTTTGG T G DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:20661235..20661400 26863196 MeRIP-seq:(Medium) rs1166127455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1128,Human_RBP_ID_224844,Human_RBP_ID_339885,Human_RBP_ID_745898,Human_RBP_ID_4020830,Human_RBP_ID_22428188,Human_RBP_ID_23122086,Human_RBP_ID_26851368 63667 RMVar_ID_63667 Human_SNP_ID_5549088 m1A Human chr1 - 20661350 20661350 20661350 CACGTGCTGGGTCCTTCGGCAGGAGGAGGAAGATGGAGCCCAGCACCGCGGCCCGGGCTTGGGCC CACGTGCTGGGTCCTTCGGCAGGAGGAGGAAGGTGGAGCCCAGCACCGCGGCCCGGGCTTGGGCC T C DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:20661235..20661375 26863196 MeRIP-seq:(Medium) rs764714304 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1128,Human_RBP_ID_224844,Human_RBP_ID_339885,Human_RBP_ID_745898,Human_RBP_ID_4020833,Human_RBP_ID_22428188,Human_RBP_ID_23122086 63668 RMVar_ID_63668 Human_SNP_ID_5568320 m1A Human chr1 - 20728060 20728060 20728060 TTGCAGCCTCCCCTCCCGTGGAGCTGGAAGCCAGGCACCCTGGGGGCCATGCAGAAGGCGGGGGC TTGCAGCCTCCCCTCCCGTGGAGCTGGAAGCCGGGCACCCTGGGGGCCATGCAGAAGGCGGGGGC T C SH2D5 Ensembl:ENSG00000189410 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:20728047..20728130 26863196 MeRIP-seq:(Medium) rs1274770049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340039 Human_Splice_Rec_26640,Human_Splice_Rec_26684,Human_Splice_Rec_26692,Human_Splice_Rec_26702,Human_Splice_Rec_26710 RMVar_hsa_circ_100210,RMVar_hsa_circ_129874 63669 RMVar_ID_63669 Human_SNP_ID_5575892 m1A Human chr1 - 20755406 20755406 20755406 CACCATGCCTGATTAATTTTTGTATTTTTTGTAGAAATGGGGTTTCGCCGTGTTGCCCAGGCTAC CACCATGCCTGATTAATTTTTGTATTTTTTGTGGAAATGGGGTTTCGCCGTGTTGCCCAGGCTAC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1346800979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10748954 RMVar_hsa_circ_41282,RMVar_hsa_circ_16089,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129878,RMVar_hsa_circ_129879,RMVar_hsa_circ_129883,RMVar_hsa_circ_63263,RMVar_hsa_circ_312661,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_320318,RMVar_hsa_circ_272824,RMVar_hsa_circ_129889,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890 63670 RMVar_ID_63670 Human_SNP_ID_5576261 m1A Human chr1 - 20756783 20756783 20756783 TGAACGCGGGAGGTGGAGGTTGCATTGAGCCAAGATTGCACCACTGTGCTCTAGGCTAGGTGACA TGAACGCGGGAGGTGGAGGTTGCATTGAGCCAGGATTGCACCACTGTGCTCTAGGCTAGGTGACA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1321778311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1252510,Human_RBP_ID_10749044,Human_RBP_ID_23303140 RMVar_hsa_circ_41282,RMVar_hsa_circ_16089,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129878,RMVar_hsa_circ_129879,RMVar_hsa_circ_129883,RMVar_hsa_circ_63263,RMVar_hsa_circ_312661,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_320318,RMVar_hsa_circ_272824,RMVar_hsa_circ_129889,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890 63671 RMVar_ID_63671 Human_SNP_ID_5582862 m1A Human chr1 - 20779901 20779901 20779901 TTATGGCCATCTCTTTTCTTAGAAGGTAGAAGATAGCACCATGCCGATTCGTCGAACTGTGAATT TTATGGCCATCTCTTTTCTTAGAAGGTAGAAGTTAGCACCATGCCGATTCGTCGAACTGTGAATT T A HP1BP3 Ensembl:ENSG00000127483 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:20779851..20779925 26863196 MeRIP-seq:(Medium) rs141968096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109451,Human_RBP_ID_5747503,Human_RBP_ID_9355619,Human_RBP_ID_10749781,Human_RBP_ID_22749872,Human_RBP_ID_27797479 Human_Splice_Rec_26720,Human_Splice_Rec_26721,Human_Splice_Rec_26742,Human_Splice_Rec_26743,Human_Splice_Rec_26798,Human_Splice_Rec_26799,Human_Splice_Rec_26812,Human_Splice_Rec_26813,Human_Splice_Rec_26818,Human_Splice_Rec_26819,Human_Splice_Rec_26824,Human_Splice_Rec_26825,Human_Splice_Rec_26832,Human_Splice_Rec_26833,Human_Splice_Rec_26836,Human_Splice_Rec_26837,Human_Splice_Rec_26842,Human_Splice_Rec_26843,Human_Splice_Rec_26846 Human_miRNA_ID_2491915 RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_335005,RMVar_hsa_circ_337821,RMVar_hsa_circ_21434,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_129897,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_129900,RMVar_hsa_circ_129901,RMVar_hsa_circ_275156,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_129913,RMVar_hsa_circ_99387,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914,RMVar_hsa_circ_129915,RMVar_hsa_circ_313807,RMVar_hsa_circ_315643 63672 RMVar_ID_63672 Human_SNP_ID_5584898 m1A Human chr1 + 20786417 20786417 20786417 GAAGGCCGCGGGAAGGACGGCAAGAGCAGCGGAGACAAAGCAGCGAGGCGAGGTAGCTACAGGCC GAAGGCCGCGGGAAGGACGGCAAGAGCAGCGGCGACAAAGCAGCGAGGCGAGGTAGCTACAGGCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:20786401..20786630 26863196 MeRIP-seq:(Medium) rs1196458059 Functional Loss SNV dbSNP153 33..33 33 - - - 63673 RMVar_ID_63673 Human_SNP_ID_5584916 m1A Human chr1 + 20786450 20786450 20786450 GACAAAGCAGCGAGGCGAGGTAGCTACAGGCCACAGCGGCGAACGCGCACGGCGGGGGAGAGCGC GACAAAGCAGCGAGGCGAGGTAGCTACAGGCCGCAGCGGCGAACGCGCACGGCGGGGGAGAGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20786447..20786634 26863196 MeRIP-seq:(Medium) rs749084391 Functional Loss SNV dbSNP153 33..33 33 - - - 63674 RMVar_ID_63674 Human_SNP_ID_5584917 m1A Human chr1 + 20786450 20786450 20786450 GACAAAGCAGCGAGGCGAGGTAGCTACAGGCCACAGCGGCGAACGCGCACGGCGGGGGAGAGCGC GACAAAGCAGCGAGGCGAGGTAGCTACAGGCCTCAGCGGCGAACGCGCACGGCGGGGGAGAGCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:20786447..20786634 26863196 MeRIP-seq:(Medium) rs749084391 Functional Loss SNV dbSNP153 33..33 33 - - - 63675 RMVar_ID_63675 Human_SNP_ID_5584919 m1A Human chr1 + 20786452 20786452 20786452 CAAAGCAGCGAGGCGAGGTAGCTACAGGCCACAGCGGCGAACGCGCACGGCGGGGGAGAGCGCGG CAAAGCAGCGAGGCGAGGTAGCTACAGGCCACCGCGGCGAACGCGCACGGCGGGGGAGAGCGCGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr1:20786425..20786581;chr1:20786451..20786633 26863196 MeRIP-seq:(Medium) rs1253193178 Functional Loss SNV dbSNP153 33..33 33 - - - 63676 RMVar_ID_63676 Human_SNP_ID_5584927 m1A Human chr1 + 20786478 20786478 20786478 GGCCACAGCGGCGAACGCGCACGGCGGGGGAGAGCGCGGGCCGCCAGCGAGGCGGGGAAAGCTCG GGCCACAGCGGCGAACGCGCACGGCGGGGGAGGGCGCGGGCCGCCAGCGAGGCGGGGAAAGCTCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:20786477..20786619 26863196 MeRIP-seq:(Medium) rs1472607876 Functional Loss SNV dbSNP153 33..33 33 - - - 63677 RMVar_ID_63677 Human_SNP_ID_5585279 m1A Human chr1 - 20787191 20787191 20787191 GCGGGCGCCAGGACCGGCCGAACGCAGAGGTAACGCAGGACCGAACAGGCGGCCGGGGAGTGGGC GCGGGCGCCAGGACCGGCCGAACGCAGAGGTAGCGCAGGACCGAACAGGCGGCCGGGGAGTGGGC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:20787176..20787250 26863196 MeRIP-seq:(Medium) rs1445418495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5334933,Human_RBP_ID_18415446,Human_RBP_ID_19037064,Human_RBP_ID_23117634 Human_miRNA_ID_1978242 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 63678 RMVar_ID_63678 Human_SNP_ID_5585314 m1A Human chr1 + 20787275 20787256 20787275 CGCCGCTCCCGCCGCCGCTAGTCGCCTCCGCCACCGCTGTCCTCCAGTCCCAGCCGCCGAGCTCT CGCCGCTCCCGCCG___________________CCGCTGTCCTCCAGTCCCAGCCGCCGAGCTCT GCCGCTAGTCGCCTCCGCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:20787164..20787308 26863196 MeRIP-seq:(Medium) rs1045849000 Functional Loss DEL dbSNP153 15..33 33 - - - 63679 RMVar_ID_63679 Human_SNP_ID_5585317 m1A Human chr1 - 20787261 20787261 20787261 GGGACTGGAGGACAGCGGTGGCGGAGGCGACTAGCGGCGGCGGGAGCGGCGCCGAGAGGCCGTGC GGGACTGGAGGACAGCGGTGGCGGAGGCGACTGGCGGCGGCGGGAGCGGCGCCGAGAGGCCGTGC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:20787149..20787300 26863196 MeRIP-seq:(Medium) rs1472474214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804264,Human_RBP_ID_4021410,Human_RBP_ID_5747612,Human_RBP_ID_9318665,Human_RBP_ID_18414879,Human_RBP_ID_18967524,Human_RBP_ID_26310393 Human_Splice_Rec_26717,Human_Splice_Rec_26797,Human_Splice_Rec_26829 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 63680 RMVar_ID_63680 Human_SNP_ID_5585318 m1A Human chr1 - 20787264 20787264 20787264 GCTGGGACTGGAGGACAGCGGTGGCGGAGGCGACTAGCGGCGGCGGGAGCGGCGCCGAGAGGCCG GCTGGGACTGGAGGACAGCGGTGGCGGAGGCGGCTAGCGGCGGCGGGAGCGGCGCCGAGAGGCCG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:20787157..20787325;chr1:20787151..20787325;chr1:20787143..20787325;chr1:20787201..20787325 26863196 MeRIP-seq:(Medium) rs538162176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804264,Human_RBP_ID_4021410,Human_RBP_ID_5747612,Human_RBP_ID_9318665,Human_RBP_ID_18414879,Human_RBP_ID_18967524,Human_RBP_ID_26310393 Human_Splice_Rec_26717,Human_Splice_Rec_26797,Human_Splice_Rec_26829 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 63681 RMVar_ID_63681 Human_SNP_ID_5585324 m1A Human chr1 + 20787275 20787275 20787275 CGCCGCTCCCGCCGCCGCTAGTCGCCTCCGCCACCGCTGTCCTCCAGTCCCAGCCGCCGAGCTCT CGCCGCTCCCGCCGCCGCTAGTCGCCTCCGCCGCCGCTGTCCTCCAGTCCCAGCCGCCGAGCTCT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:20787164..20787308 26863196 MeRIP-seq:(Medium) rs1172345099 Functional Loss SNV dbSNP153 33..33 33 - - - 63682 RMVar_ID_63682 Human_SNP_ID_5604002 m1A Human chr1 - 20860434 20860434 20860434 ATTCACAAAGAGGCTAAAATAGAAGAACAAGAAGAGCAAAGGAAGGTCCAGCAACTCATGACCAA ATTCACAAAGAGGCTAAAATAGAAGAACAAGACGAGCAAAGGAAGGTCCAGCAACTCATGACCAA T G EIF4G3 Ensembl:ENSG00000075151 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20860346..20860464 26863196 MeRIP-seq:(Medium) rs1288203556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17546,Human_RBP_ID_854027,Human_RBP_ID_1734704,Human_RBP_ID_3932949,Human_RBP_ID_5537285,Human_RBP_ID_18967526,Human_RBP_ID_26313509 Human_Splice_Rec_26884,Human_Splice_Rec_26885,Human_Splice_Rec_26944,Human_Splice_Rec_26945,Human_Splice_Rec_27012,Human_Splice_Rec_27013,Human_Splice_Rec_27080,Human_Splice_Rec_27081,Human_Splice_Rec_27146,Human_Splice_Rec_27147 Human_miRNA_ID_1767056 RMVar_hsa_circ_4645,RMVar_hsa_circ_102016,RMVar_hsa_circ_129920,RMVar_hsa_circ_122553,RMVar_hsa_circ_113254,RMVar_hsa_circ_66038,RMVar_hsa_circ_129924,RMVar_hsa_circ_129925,RMVar_hsa_circ_129923,RMVar_hsa_circ_36834,RMVar_hsa_circ_313305,RMVar_hsa_circ_129927,RMVar_hsa_circ_120181,RMVar_hsa_circ_370451,RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_32922,RMVar_hsa_circ_44922,RMVar_hsa_circ_129931,RMVar_hsa_circ_129932,RMVar_hsa_circ_129930,RMVar_hsa_circ_40386,RMVar_hsa_circ_129928,RMVar_hsa_circ_31337,RMVar_hsa_circ_74068,RMVar_hsa_circ_41188,RMVar_hsa_circ_277309,RMVar_hsa_circ_355098,RMVar_hsa_circ_339179,RMVar_hsa_circ_283644,RMVar_hsa_circ_129937,RMVar_hsa_circ_129938,RMVar_hsa_circ_365832,RMVar_hsa_circ_338122,RMVar_hsa_circ_358241,RMVar_hsa_circ_43998,RMVar_hsa_circ_58017,RMVar_hsa_circ_129939,RMVar_hsa_circ_129940,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_76854,RMVar_hsa_circ_364634,RMVar_hsa_circ_39504,RMVar_hsa_circ_56936,RMVar_hsa_circ_129944,RMVar_hsa_circ_129943,RMVar_hsa_circ_293791,RMVar_hsa_circ_354001,RMVar_hsa_circ_363379,RMVar_hsa_circ_129945,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_335747,RMVar_hsa_circ_298726,RMVar_hsa_circ_65525,RMVar_hsa_circ_356832,RMVar_hsa_circ_129947,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_129948,RMVar_hsa_circ_366470,RMVar_hsa_circ_376856,RMVar_hsa_circ_15884 63683 RMVar_ID_63683 Human_SNP_ID_5658719 m1A Human chr1 - 21083911 21083911 21083911 GGTGGTGTCGTAGATCTTGGTTTGGGCAACTGAGTGGTCCTATTTGTGGAGATGAATACTGAATG GGTGGTGTCGTAGATCTTGGTTTGGGCAACTGGGTGGTCCTATTTGTGGAGATGAATACTGAATG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21083909..21083981 26863196 MeRIP-seq:(Medium) rs922172791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1134,Human_RBP_ID_23362345 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_69401,RMVar_hsa_circ_361048,RMVar_hsa_circ_270139,RMVar_hsa_circ_129971,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_129979,RMVar_hsa_circ_129982,RMVar_hsa_circ_365884,RMVar_hsa_circ_317867,RMVar_hsa_circ_129983,RMVar_hsa_circ_333328,RMVar_hsa_circ_277928,RMVar_hsa_circ_129991,RMVar_hsa_circ_129984,RMVar_hsa_circ_129985,RMVar_hsa_circ_104222,RMVar_hsa_circ_302688,RMVar_hsa_circ_334495,RMVar_hsa_circ_93832,RMVar_hsa_circ_129996,RMVar_hsa_circ_129997,RMVar_hsa_circ_360070,RMVar_hsa_circ_285564,RMVar_hsa_circ_129999,RMVar_hsa_circ_129998,RMVar_hsa_circ_288290,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_270666,RMVar_hsa_circ_130003,RMVar_hsa_circ_303313,RMVar_hsa_circ_130006,RMVar_hsa_circ_130007,RMVar_hsa_circ_130005,RMVar_hsa_circ_278443,RMVar_hsa_circ_281334,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130015,RMVar_hsa_circ_83587,RMVar_hsa_circ_130016,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_33465,RMVar_hsa_circ_130010,RMVar_hsa_circ_130019 63684 RMVar_ID_63684 Human_SNP_ID_5658720 m1A Human chr1 - 21083911 21083911 21083911 GGTGGTGTCGTAGATCTTGGTTTGGGCAACTGAGTGGTCCTATTTGTGGAGATGAATACTGAATG GGTGGTGTCGTAGATCTTGGTTTGGGCAACTGCGTGGTCCTATTTGTGGAGATGAATACTGAATG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21083909..21083981 26863196 MeRIP-seq:(Medium) rs922172791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1134,Human_RBP_ID_23362345 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_69401,RMVar_hsa_circ_361048,RMVar_hsa_circ_270139,RMVar_hsa_circ_129971,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_129979,RMVar_hsa_circ_129982,RMVar_hsa_circ_365884,RMVar_hsa_circ_317867,RMVar_hsa_circ_129983,RMVar_hsa_circ_333328,RMVar_hsa_circ_277928,RMVar_hsa_circ_129991,RMVar_hsa_circ_129984,RMVar_hsa_circ_129985,RMVar_hsa_circ_104222,RMVar_hsa_circ_302688,RMVar_hsa_circ_334495,RMVar_hsa_circ_93832,RMVar_hsa_circ_129996,RMVar_hsa_circ_129997,RMVar_hsa_circ_360070,RMVar_hsa_circ_285564,RMVar_hsa_circ_129999,RMVar_hsa_circ_129998,RMVar_hsa_circ_288290,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_270666,RMVar_hsa_circ_130003,RMVar_hsa_circ_303313,RMVar_hsa_circ_130006,RMVar_hsa_circ_130007,RMVar_hsa_circ_130005,RMVar_hsa_circ_278443,RMVar_hsa_circ_281334,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130015,RMVar_hsa_circ_83587,RMVar_hsa_circ_130016,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_33465,RMVar_hsa_circ_130010,RMVar_hsa_circ_130019 63685 RMVar_ID_63685 Human_SNP_ID_5658722 m1A Human chr1 - 21083915 21083915 21083915 TAAAGGTGGTGTCGTAGATCTTGGTTTGGGCAACTGAGTGGTCCTATTTGTGGAGATGAATACTG TAAAGGTGGTGTCGTAGATCTTGGTTTGGGCAGCTGAGTGGTCCTATTTGTGGAGATGAATACTG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:21083912..21084022 26863196 MeRIP-seq:(Medium) rs936285519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1134,Human_RBP_ID_23362345 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_69401,RMVar_hsa_circ_361048,RMVar_hsa_circ_270139,RMVar_hsa_circ_129971,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_129979,RMVar_hsa_circ_129982,RMVar_hsa_circ_365884,RMVar_hsa_circ_317867,RMVar_hsa_circ_129983,RMVar_hsa_circ_333328,RMVar_hsa_circ_277928,RMVar_hsa_circ_129991,RMVar_hsa_circ_129984,RMVar_hsa_circ_129985,RMVar_hsa_circ_104222,RMVar_hsa_circ_302688,RMVar_hsa_circ_334495,RMVar_hsa_circ_93832,RMVar_hsa_circ_129996,RMVar_hsa_circ_129997,RMVar_hsa_circ_360070,RMVar_hsa_circ_285564,RMVar_hsa_circ_129999,RMVar_hsa_circ_129998,RMVar_hsa_circ_288290,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_270666,RMVar_hsa_circ_130003,RMVar_hsa_circ_303313,RMVar_hsa_circ_130006,RMVar_hsa_circ_130007,RMVar_hsa_circ_130005,RMVar_hsa_circ_278443,RMVar_hsa_circ_281334,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130015,RMVar_hsa_circ_83587,RMVar_hsa_circ_130016,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_33465,RMVar_hsa_circ_130010,RMVar_hsa_circ_130019 63686 RMVar_ID_63686 Human_SNP_ID_5676438 m1A Human chr1 - 21156243 21156243 21156243 AGGATCAACGCAGCACAACCTTTAAACTATCCAGAATAGATTCCCACTGAGTTTTGTTTATGTAA AGGATCAACGCAGCACAACCTTTAAACTATCCGGAATAGATTCCCACTGAGTTTTGTTTATGTAA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21156241..21156411 26863196 MeRIP-seq:(Medium) rs1349472354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5754414 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_83587,RMVar_hsa_circ_130013,RMVar_hsa_circ_130012,RMVar_hsa_circ_130010,RMVar_hsa_circ_125788,RMVar_hsa_circ_130023,RMVar_hsa_circ_130024 63687 RMVar_ID_63687 Human_SNP_ID_5678905 m1A Human chr1 + 21166044 21166044 21166044 ACTACACTTGCTTCAGGCCCAAATCTTTGTTCATATTGATCACCCACTCATCATAATCCACCCAC ACTACACTTGCTTCAGGCCCAAATCTTTGTTCGTATTGATCACCCACTCATCATAATCCACCCAC A G lnc-NBPF3-8 RNACentral:URS00008BE365 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:21166017..21166156 26863196 MeRIP-seq:(Medium) rs1417018036 Functional Loss SNV dbSNP153 33..33 33 - - - 63688 RMVar_ID_63688 Human_SNP_ID_5681571 m1A Human chr1 + 21176226 21176226 21176226 GGAGGGCCCTGATGTTCGGGTGAGGAGGGGGGACCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC GGAGGGCCCTGATGTTCGGGTGAGGAGGGGGGGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:21176081..21176470;chr1:21176098..21176405;chr1:21176129..21176410 26863196 MeRIP-seq:(Medium) rs923405496 Functional Loss SNV dbSNP153 33..33 33 - - - 63689 RMVar_ID_63689 Human_SNP_ID_5681615 m1A Human chr1 - 21176270 21176237 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC_________________________________ CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs1469784361 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63690 RMVar_ID_63690 Human_SNP_ID_5681623 m1A Human chr1 - 21176270 21176243 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC___________________________GGCGGC CGCCGCCGCCGCCGCCGCCGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs767011350 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63691 RMVar_ID_63691 Human_SNP_ID_5681627 m1A Human chr1 - 21176270 21176246 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC________________________GGCGGCGGC CGCCGCCGCCGCCGCCGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs760373868 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63692 RMVar_ID_63692 Human_SNP_ID_5681635 m1A Human chr1 - 21176270 21176252 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC__________________GGCGGCGGCGGCGGC CGCCGCCGCCGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs763852304 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63693 RMVar_ID_63693 Human_SNP_ID_5681643 m1A Human chr1 - 21176270 21176258 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC____________GGCGGCGGCGGCGGCGGCGGC CGCCGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs921068712 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63694 RMVar_ID_63694 Human_SNP_ID_5681650 m1A Human chr1 - 21176270 21176261 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC_________GGCGGCGGCGGCGGCGGCGGCGGC CGCCGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs1345978076 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63695 RMVar_ID_63695 Human_SNP_ID_5681657 m1A Human chr1 - 21176270 21176264 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC______GGCGGCGGCGGCGGCGGCGGCGGCGGC CGCTGCT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs757105157 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63696 RMVar_ID_63696 Human_SNP_ID_5681658 m1A Human chr1 - 21176270 21176264 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC___AGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CGCTGCT CGCT EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs757105157 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63697 RMVar_ID_63697 Human_SNP_ID_5681667 m1A Human chr1 - 21176270 21176269 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGC_GCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CT C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs1169144631 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63698 RMVar_ID_63698 Human_SNP_ID_5681669 m1A Human chr1 - 21176270 21176270 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs749796228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63699 RMVar_ID_63699 Human_SNP_ID_5681670 m1A Human chr1 - 21176270 21176270 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCCGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T G EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs749796228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63700 RMVar_ID_63700 Human_SNP_ID_5681680 m1A Human chr1 + 21176288 21176288 21176288 GCCGCCGCCGCTGCTGCCGCCGCCGGGTGAGGAGGCGGTACCGCTGCTGCCGCCGCCGCCGCCGC GCCGCCGCCGCTGCTGCCGCCGCCGGGTGAGGCGGCGGTACCGCTGCTGCCGCCGCCGCCGCCGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr1:21176251..21176300;chr1:21176241..21176409 26863196 MeRIP-seq:(Medium) rs1158330389 Functional Loss SNV dbSNP153 33..33 33 - - - 63701 RMVar_ID_63701 Human_SNP_ID_5681689 m1A Human chr1 - 21176303 21176303 21176303 GGACCCGGCACCGGAGCGGCGGCGGCGGCGGCAGCAGCGGTACCGCCTCCTCACCCGGCGGCGGC GGACCCGGCACCGGAGCGGCGGCGGCGGCGGCTGCAGCGGTACCGCCTCCTCACCCGGCGGCGGC T A EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:21176222..21176309 26863410 MeRIP-seq:(Medium) rs1305079620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95834,Human_RBP_ID_4023929,Human_RBP_ID_22871577,Human_RBP_ID_23255315 Human_Splice_Rec_26848,Human_Splice_Rec_26972,Human_Splice_Rec_27040,Human_Splice_Rec_27108,Human_Splice_Rec_27218,Human_Splice_Rec_27236,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63702 RMVar_ID_63702 Human_SNP_ID_5681690 m1A Human chr1 - 21176303 21176303 21176303 GGACCCGGCACCGGAGCGGCGGCGGCGGCGGCAGCAGCGGTACCGCCTCCTCACCCGGCGGCGGC GGACCCGGCACCGGAGCGGCGGCGGCGGCGGCGGCAGCGGTACCGCCTCCTCACCCGGCGGCGGC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:21176222..21176309 26863410 MeRIP-seq:(Medium) rs1305079620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95834,Human_RBP_ID_4023929,Human_RBP_ID_22871577,Human_RBP_ID_23255315 Human_Splice_Rec_26848,Human_Splice_Rec_26972,Human_Splice_Rec_27040,Human_Splice_Rec_27108,Human_Splice_Rec_27218,Human_Splice_Rec_27236,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 63703 RMVar_ID_63703 Human_SNP_ID_5681779 m1A Human chr1 + 21176567 21176564 21176567 AGGAGGGGGCCGGGGCCGGTCACACACGCCCGACGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCG AGGAGGGGGCCGGGGCCGGTCACACACGCC___CGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCG CCGA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:21176512..21176622 26863410 MeRIP-seq:(Medium) rs1462752919 Functional Loss DEL dbSNP153 31..33 33 - - - 63704 RMVar_ID_63704 Human_SNP_ID_5681781 m1A Human chr1 + 21176567 21176567 21176567 AGGAGGGGGCCGGGGCCGGTCACACACGCCCGACGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCG AGGAGGGGGCCGGGGCCGGTCACACACGCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:21176512..21176622 26863410 MeRIP-seq:(Medium) rs1047155960 Functional Loss SNV dbSNP153 33..33 33 - - - 63705 RMVar_ID_63705 Human_SNP_ID_5681798 m1A Human chr1 - 21176593 21176569 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG________________________CGTCGGGCG GCCGCCGCCGCCGCCGCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs989319218 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63706 RMVar_ID_63706 Human_SNP_ID_5681800 m1A Human chr1 + 21176620 21176571 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG _________________________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGCCGCCGCCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1419440094 Functional Loss DEL dbSNP153 1..33 33 - - - 63707 RMVar_ID_63707 Human_SNP_ID_5681802 m1A Human chr1 - 21176593 21176572 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG_____________________CGGCGTCGGGCG GCCGCCGCCGCCGCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1349138801 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63708 RMVar_ID_63708 Human_SNP_ID_5681804 m1A Human chr1 + 21176620 21176574 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG _________________________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGCCGCCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1434059326 Functional Loss DEL dbSNP153 1..33 33 - - - 63709 RMVar_ID_63709 Human_SNP_ID_5681806 m1A Human chr1 - 21176593 21176575 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG__________________CGGCGGCGTCGGGCG GCCGCCGCCGCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1290372317 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63710 RMVar_ID_63710 Human_SNP_ID_5681809 m1A Human chr1 + 21176620 21176577 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG _________________________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGCCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1362578292 Functional Loss DEL dbSNP153 1..33 33 - - - 63711 RMVar_ID_63711 Human_SNP_ID_5681810 m1A Human chr1 - 21176593 21176578 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG_______________CGGCGGCGGCGTCGGGCG GCCGCCGCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1245472341 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63712 RMVar_ID_63712 Human_SNP_ID_5681814 m1A Human chr1 + 21176620 21176580 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG _________________________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1217874167 Functional Loss DEL dbSNP153 1..33 33 - - - 63713 RMVar_ID_63713 Human_SNP_ID_5681815 m1A Human chr1 - 21176593 21176581 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG____________CGGCGGCGGCGGCGTCGGGCG GCCGCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1277710024 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63714 RMVar_ID_63714 Human_SNP_ID_5681816 m1A Human chr1 - 21176593 21176584 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG_________CGGCGGCGGCGGCGGCGTCGGGCG GCCGCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs888496129 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63715 RMVar_ID_63715 Human_SNP_ID_5681818 m1A Human chr1 + 21176620 21176586 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG _________________________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1480943982 Functional Loss DEL dbSNP153 1..33 33 - - - 63716 RMVar_ID_63716 Human_SNP_ID_5681820 m1A Human chr1 - 21176593 21176587 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGG______CGGCGGCGGCGGCGGCGGCGTCGGGCG GCCGCCT G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1290827919 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63717 RMVar_ID_63717 Human_SNP_ID_5681822 m1A Human chr1 - 21176593 21176593 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1443808873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 63718 RMVar_ID_63718 Human_SNP_ID_5681830 m1A Human chr1 + 21176620 21176598 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CCGCCTCCGCC______________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1404282987 Functional Loss DEL dbSNP153 12..33 33 - - - 63719 RMVar_ID_63719 Human_SNP_ID_5681832 m1A Human chr1 + 21176620 21176601 21176620 CCGCCTCCGCCGCCGCCGCCGCCGGCAGCAGCAGCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CCGCCTCCGCCGCC___________________GCCGCCCCGCGGGCCAGCACCACCGGCTGCCG CGCCGCCGCCGGCAGCAGCA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:21176525..21176675 26863410 MeRIP-seq:(Medium) rs1337621484 Functional Loss DEL dbSNP153 15..33 33 - - - 63720 RMVar_ID_63720 Human_SNP_ID_5702501 m1A Human chr1 - 21256074 21256074 21256074 GCTGGGGAAGCTGCTGGGCGGCGGGGACGAGGAGGCCATCCGGCCCCAGATGCAGCAGATCTTGG GCTGGGGAAGCTGCTGGGCGGCGGGGACGAGGTGGCCATCCGGCCCCAGATGCAGCAGATCTTGG T A ECE1 Ensembl:ENSG00000117298 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21256023..21257579 32194978 MeRIP-seq:(Medium) rs771381721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3935426,Human_RBP_ID_17765142,Human_RBP_ID_18468504,Human_RBP_ID_22750796 Human_Splice_Rec_27278,Human_Splice_Rec_27314,Human_Splice_Rec_27350,Human_Splice_Rec_27384,Human_Splice_Rec_27422,Human_Splice_Rec_27454,Human_Splice_Rec_27490,Human_Splice_Rec_27510 RMVar_hsa_circ_92267,RMVar_hsa_circ_130028,RMVar_hsa_circ_4719,RMVar_hsa_circ_39619,RMVar_hsa_circ_28078,RMVar_hsa_circ_343442,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_373834,RMVar_hsa_circ_70604,RMVar_hsa_circ_130036,RMVar_hsa_circ_130037,RMVar_hsa_circ_297219,RMVar_hsa_circ_306057,RMVar_hsa_circ_130038,RMVar_hsa_circ_334830,RMVar_hsa_circ_340974,RMVar_hsa_circ_45849 63721 RMVar_ID_63721 Human_SNP_ID_5718268 m1A Human chr1 - 21319687 21319687 21319687 CCGGTGCCTGGTAGGGAGTGGCGAGAATGAGGAGCCAGGTCTCAGGAGAGGCTGAGGAGAGTTGG CCGGTGCCTGGTAGGGAGTGGCGAGAATGAGGTGCCAGGTCTCAGGAGAGGCTGAGGAGAGTTGG T A ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21319658..21319815 26863196 MeRIP-seq:(Medium) rs1420403381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63722 RMVar_ID_63722 Human_SNP_ID_5718269 m1A Human chr1 - 21319687 21319687 21319687 CCGGTGCCTGGTAGGGAGTGGCGAGAATGAGGAGCCAGGTCTCAGGAGAGGCTGAGGAGAGTTGG CCGGTGCCTGGTAGGGAGTGGCGAGAATGAGGGGCCAGGTCTCAGGAGAGGCTGAGGAGAGTTGG T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21319658..21319815 26863196 MeRIP-seq:(Medium) rs1420403381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63723 RMVar_ID_63723 Human_SNP_ID_5718548 m1A Human chr1 - 21320753 21320753 21320753 TCCGCAGAATGAAGGAAGGGTGGGGAAGAAAGACACAGAGATGAGGCTGCGGCCCCTATAGGAGC TCCGCAGAATGAAGGAAGGGTGGGGAAGAAAGGCACAGAGATGAGGCTGCGGCCCCTATAGGAGC T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21320750..21320816 26863196 MeRIP-seq:(Medium) rs987219833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63724 RMVar_ID_63724 Human_SNP_ID_5722098 m1A Human chr1 - 21334836 21334836 21334836 CCTCAGGATATTCGTCTGTCCTGAGGCTGAGGAGGCGTAGGTTTCTGCAGGATCTGGGATTTTGG CCTCAGGATATTCGTCTGTCCTGAGGCTGAGGGGGCGTAGGTTTCTGCAGGATCTGGGATTTTGG T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:21334831..21335357;chr1:21334831..21335352 26863196 MeRIP-seq:(Medium) rs943257026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63725 RMVar_ID_63725 Human_SNP_ID_5722099 m1A Human chr1 - 21334836 21334836 21334836 CCTCAGGATATTCGTCTGTCCTGAGGCTGAGGAGGCGTAGGTTTCTGCAGGATCTGGGATTTTGG CCTCAGGATATTCGTCTGTCCTGAGGCTGAGGCGGCGTAGGTTTCTGCAGGATCTGGGATTTTGG T G ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:21334831..21335357;chr1:21334831..21335352 26863196 MeRIP-seq:(Medium) rs943257026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63726 RMVar_ID_63726 Human_SNP_ID_5724652 m1A Human chr1 - 21345318 21345303 21345318 TCCGGTCCAGCCCAGCCTCGACGGTCGCGGGCAGCGGTGCCGCGGGTGGCACCCGGGGCCGCCCT TCCGGTCCAGCCCAGCCTCGACGGTCGCGGGC_______________GGCACCCGGGGCCGCCCT CACCCGCGGCACCGCT C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21345317..21345550 26863196 MeRIP-seq:(Medium) rs1331576261 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_26774122 RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 63727 RMVar_ID_63727 Human_SNP_ID_5724845 m1A Human chr1 + 21345755 21345755 21345755 GCTTCGGGGCGCAGGGTCCAGACCTTGCCGAGACCGGCGTTGGGAGCTAGCAGAACCGGGAAGAG GCTTCGGGGCGCAGGGTCCAGACCTTGCCGAGTCCGGCGTTGGGAGCTAGCAGAACCGGGAAGAG A T lnc-NBPF3-11,lnc-NBPF3-11:2,lnc-NBPF3-11:3 RNACentral:URS0000D57E37,RNACentral:URS0000D5B64A,RNACentral:URS0000D578C9 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21345708..21345873 26863196 MeRIP-seq:(Medium) rs533931604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23363529 63728 RMVar_ID_63728 Human_SNP_ID_5724870 m1A Human chr1 - 21345830 21345830 21345830 ACACTCCAGTGCAGGAGCCAGGCAGGAGACAAAGGTCGCCGAGGCTCCCGGCGGCCCCACCGGAC ACACTCCAGTGCAGGAGCCAGGCAGGAGACAACGGTCGCCGAGGCTCCCGGCGGCCCCACCGGAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:21345683..21345863 26863196 MeRIP-seq:(Medium) rs1238736628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4024304 63729 RMVar_ID_63729 Human_SNP_ID_5726750 m1A Human chr1 + 21352341 21352341 21352341 GGGAGAGGCTGGAGCAGGGGATGAAGTGGGTCAAAGCCAGCGCAGGCTGAGCTTTGAGGGAGTGT GGGAGAGGCTGGAGCAGGGGATGAAGTGGGTCGAAGCCAGCGCAGGCTGAGCTTTGAGGGAGTGT A G lnc-NBPF3-11 RNACentral:URS0000D57E37 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21352291..21352478 26863196 MeRIP-seq:(Medium) rs749807751 Functional Loss SNV dbSNP153 33..33 33 - - - 63730 RMVar_ID_63730 Human_SNP_ID_5746360 m1A Human chr1 - 21426289 21426289 21426289 CCAGAACTGCCTGATTCATGCCAGCCCTACGGAAGTTGCTTTTACTCATTGGAGGAAGAACACGT CCAGAACTGCCTGATTCATGCCAGCCCTACGGCAGTTGCTTTTACTCATTGGAGGAAGAACACGT T G NBPF2P Ensembl:ENSG00000227001 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs140348908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108762,RMVar_hsa_circ_130049,RMVar_hsa_circ_103959,RMVar_hsa_circ_130048 63731 RMVar_ID_63731 Human_SNP_ID_5760628 m1A Human chr1 + 21484370 21484370 21484370 ATCTTTTTGTTGTTGTCATTGATTTTGGTGACATGGACTTGTTTGTAGAGGACAGGTCAGCTGTC ATCTTTTTGTTGTTGTCATTGATTTTGGTGACGTGGACTTGTTTGTAGAGGACAGGTCAGCTGTC A G NBPF3 Ensembl:ENSG00000142794 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1157097809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5756401 63732 RMVar_ID_63732 Human_SNP_ID_5766896 m1A Human chr1 + 21509442 21509442 21509442 GGTGGTGGCCCGGGCCGCGTTGCGCTCCCGCCACTCCGCGCCCGCTATCCTGGCTCCGTGCTCCC GGTGGTGGCCCGGGCCGCGTTGCGCTCCCGCCCCTCCGCGCCCGCTATCCTGGCTCCGTGCTCCC A C ALPL Ensembl:ENSG00000162551 Protein coding exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:21509383..21509465 26863410 MeRIP-seq:(Medium) rs1226003447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_27781,Human_Splice_Rec_27789,Human_Splice_Rec_27811,Human_Splice_Rec_27829 63733 RMVar_ID_63733 Human_SNP_ID_5783212 m1A Human chr1 + 21573678 21573678 21573678 CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCAGGGGACATGCAGTACGAGCTGAACAGGAACAA CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCGGGGGACATGCAGTACGAGCTGAACAGGAACAA A G ALPL Ensembl:ENSG00000162551 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3200255 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_27804,Human_Splice_Rec_27822,Human_Splice_Rec_27842,Human_Splice_Rec_27864 Clinvar_Rec_237,Clinvar_Rec_238 GWAS_ID_7750,GWAS_ID_7751,GWAS_ID_7752,GWAS_ID_7753,GWAS_ID_7754 RMVar_hsa_circ_12620 63734 RMVar_ID_63734 Human_SNP_ID_5783213 m1A Human chr1 + 21573678 21573678 21573678 CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCAGGGGACATGCAGTACGAGCTGAACAGGAACAA CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCTGGGGACATGCAGTACGAGCTGAACAGGAACAA A T ALPL Ensembl:ENSG00000162551 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3200255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_27804,Human_Splice_Rec_27822,Human_Splice_Rec_27842,Human_Splice_Rec_27864 Clinvar_Rec_237,Clinvar_Rec_238 GWAS_ID_7750,GWAS_ID_7751,GWAS_ID_7752,GWAS_ID_7753,GWAS_ID_7754 RMVar_hsa_circ_12620 63735 RMVar_ID_63735 Human_SNP_ID_5789641 m1A Human chr1 - 21596892 21596892 21596892 AGCTCCGTGTGGAGAGCTTAGCCCCTGGAGGCAGCACAAGGAGGATGTGATATGTGGGGGAGTGA AGCTCCGTGTGGAGAGCTTAGCCCCTGGAGGCGGCACAAGGAGGATGTGATATGTGGGGGAGTGA T C RAP1GAP Ensembl:ENSG00000076864 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21596844..21596952 26863196 MeRIP-seq:(Medium) rs760043348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8170175,Human_RBP_ID_26385458 63736 RMVar_ID_63736 Human_SNP_ID_5804432 m1A Human chr1 - 21651819 21651819 21651819 GGGCCGGGCCGGGCGGCGGCGGCGGCACCATGAGCGGCCGGAAGCGCAGCTTCACCTTCGGGGCC GGGCCGGGCCGGGCGGCGGCGGCGGCACCATGGGCGGCCGGAAGCGCAGCTTCACCTTCGGGGCC T C RAP1GAP Ensembl:ENSG00000076864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21651763..21651836 26863196 MeRIP-seq:(Medium) rs1018957293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_28023,Human_Splice_Rec_28219 RMVar_hsa_circ_29755,RMVar_hsa_circ_130060 63737 RMVar_ID_63737 Human_SNP_ID_5829111 m1A Human chr1 - 21750329 21750329 21750329 AAATGATTGAAGGTGAAGGGGTGAGCCCCGTTAGAAACAAGGAGAAGAGTGTTCTGGGTAGATGA AAATGATTGAAGGTGAAGGGGTGAGCCCCGTTGGAAACAAGGAGAAGAGTGTTCTGGGTAGATGA T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr1:21750089..21750507;chr1:21750285..21750437 26863196 MeRIP-seq:(Medium) rs1363126882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5571,RMVar_hsa_circ_116760,RMVar_hsa_circ_130061,RMVar_hsa_circ_130073,RMVar_hsa_circ_337136,RMVar_hsa_circ_5706,RMVar_hsa_circ_130080,RMVar_hsa_circ_130083,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_269122,RMVar_hsa_circ_356564,RMVar_hsa_circ_341188,RMVar_hsa_circ_130087,RMVar_hsa_circ_275100,RMVar_hsa_circ_33068,RMVar_hsa_circ_266719,RMVar_hsa_circ_58046,RMVar_hsa_circ_88666,RMVar_hsa_circ_130095,RMVar_hsa_circ_130096,RMVar_hsa_circ_265895,RMVar_hsa_circ_11237,RMVar_hsa_circ_314371,RMVar_hsa_circ_130098,RMVar_hsa_circ_276354,RMVar_hsa_circ_292997,RMVar_hsa_circ_279124,RMVar_hsa_circ_130100,RMVar_hsa_circ_266930,RMVar_hsa_circ_130099,RMVar_hsa_circ_283056,RMVar_hsa_circ_335475,RMVar_hsa_circ_351309,RMVar_hsa_circ_290204,RMVar_hsa_circ_130102,RMVar_hsa_circ_130103,RMVar_hsa_circ_130101 63738 RMVar_ID_63738 Human_SNP_ID_5833983 m1A Human chr1 - 21768684 21768684 21768684 GAGGAGAAGATGGTGACTGAGATCCTAGAAGGAAAGGGGGGGTGGGGCTTGAAAGGGGTGGGGCT GAGGAGAAGATGGTGACTGAGATCCTAGAAGGGAAGGGGGGGTGGGGCTTGAAAGGGGTGGGGCT T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21768682..21768866 26863196 MeRIP-seq:(Medium) rs1437886003 Functional Loss SNV dbSNP153 33..33 33 - - - 63739 RMVar_ID_63739 Human_SNP_ID_5837983 m1A Human chr1 + 21783029 21783029 21783029 CAGCCGCCGCCGCGGTCTGCACCGCCGCCCCAATGGGCTTCGCCACCTGCCAGCAAGGAGGACCT CAGCCGCCGCCGCGGTCTGCACCGCCGCCCCAGTGGGCTTCGCCACCTGCCAGCAAGGAGGACCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:21782826..21783148;chr1:21782913..21783160 26863196 MeRIP-seq:(Medium) rs192307625 Functional Loss SNV dbSNP153 33..33 33 - - - 63740 RMVar_ID_63740 Human_SNP_ID_5837987 m1A Human chr1 + 21783041 21783041 21783041 CGGTCTGCACCGCCGCCCCAATGGGCTTCGCCACCTGCCAGCAAGGAGGACCTGGCGCTCCTTCA CGGTCTGCACCGCCGCCCCAATGGGCTTCGCCGCCTGCCAGCAAGGAGGACCTGGCGCTCCTTCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:21782946..21783041 26863410 MeRIP-seq:(Medium) rs1334039489 Functional Loss SNV dbSNP153 33..33 33 - - - 63741 RMVar_ID_63741 Human_SNP_ID_5838014 m1A Human chr1 - 21783098 21783098 21783098 GGGCGCGGGCGGGCGCGGCGGCAGTGGCGCGCACAGGTGATTGACTGGCCAGCTGCCTGAAGGAG GGGCGCGGGCGGGCGCGGCGGCAGTGGCGCGCGCAGGTGATTGACTGGCCAGCTGCCTGAAGGAG T C USP48 Ensembl:ENSG00000090686 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:21782851..21783177 26863196 MeRIP-seq:(Medium) rs1415217306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4025707,Human_RBP_ID_8754811,Human_RBP_ID_9269907,Human_RBP_ID_9318677,Human_RBP_ID_17101674,Human_RBP_ID_17762400,Human_RBP_ID_18415933,Human_RBP_ID_23365482 63742 RMVar_ID_63742 Human_SNP_ID_5848949 m1A Human chr1 - 21822694 21822694 21822694 CCTCCTACCACGTCCTCCTGGCCTGCATTCCCACCCCCTCCTGCCAGCACACAGCCTGGGGTCCC CCTCCTACCACGTCCTCCTGGCCTGCATTCCCCCCCCCTCCTGCCAGCACACAGCCTGGGGTCCC T G HSPG2 Ensembl:ENSG00000142798 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21822643..21822808 26863196 MeRIP-seq:(Medium) rs1470276719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109021,Human_RBP_ID_17646901,Human_RBP_ID_18186901,Human_RBP_ID_18928083,Human_RBP_ID_24450239,Human_RBP_ID_26385465 Human_miRNA_ID_1700440 RMVar_hsa_circ_100643,RMVar_hsa_circ_103524,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_130107 63743 RMVar_ID_63743 Human_SNP_ID_5849178 m1A Human chr1 - 21823423 21823423 21823423 GCAGATTCTCCTCAGGCATCACAGGCTGTGTCAAGAACCTGGTGCTGCACTCGGCCCGACCCGGC GCAGATTCTCCTCAGGCATCACAGGCTGTGTCGAGAACCTGGTGCTGCACTCGGCCCGACCCGGC T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:21823275..21823425 32194978 MeRIP-seq:(Medium) rs761947438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_28792,Human_Splice_Rec_28812,Human_Splice_Rec_28814 Human_miRNA_ID_2298842,Human_miRNA_ID_2302114,Human_miRNA_ID_2305377,Human_miRNA_ID_2781967,Human_miRNA_ID_2784935 RMVar_hsa_circ_100643,RMVar_hsa_circ_103524,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_130107 63744 RMVar_ID_63744 Human_SNP_ID_5849260 m1A Human chr1 + 21823602 21823602 21823602 GGAGTGCCGTTCCTGCCCCTGCCCTGAGAAGGAGCCCCAGACTTACCGATGTAGACGCTGCCCTT GGAGTGCCGTTCCTGCCCCTGCCCTGAGAAGGGGCCCCAGACTTACCGATGTAGACGCTGCCCTT A G LDLRAD2 Ensembl:ENSG00000187942 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21823601..21823725 32194978 MeRIP-seq:(Medium) rs935060811 Functional Loss SNV dbSNP153 33..33 33 - - - 63745 RMVar_ID_63745 Human_SNP_ID_5849313 m1A Human chr1 + 21823704 21823704 21823704 CTGACCAGCTCCTCACCGTCGACTTGGATGGAACCTCTGCGGCCCTCCCTGCAGTGGAACTGGGT CTGACCAGCTCCTCACCGTCGACTTGGATGGAGCCTCTGCGGCCCTCCCTGCAGTGGAACTGGGT A G LDLRAD2 Ensembl:ENSG00000187942 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:21823701..21823725 26863196 MeRIP-seq:(Medium) rs1209865019 Functional Loss SNV dbSNP153 33..33 33 - - - 63746 RMVar_ID_63746 Human_SNP_ID_5849482 m1A Human chr1 + 21824175 21824175 21824175 ACTCGCCGTCATTGATGGGGTCCTCAGAGACCAGGCGGGCCTCCCCACTACCCAGCTGGTACCTG ACTCGCCGTCATTGATGGGGTCCTCAGAGACCCGGCGGGCCTCCCCACTACCCAGCTGGTACCTG A C LDLRAD2 Ensembl:ENSG00000187942 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21824101..21824373 32194978 MeRIP-seq:(Medium) rs1405285943 Functional Loss SNV dbSNP153 33..33 33 - - - 63747 RMVar_ID_63747 Human_SNP_ID_5850560 m1A Human chr1 + 21828189 21828189 21828189 GGGCCAGGGCAGAGGCGAGTGGGTGGGTGGGCATGGGCTGGAGGTGTCGCTGACCACCTGTGCCC GGGCCAGGGCAGAGGCGAGTGGGTGGGTGGGCCTGGGCTGGAGGTGTCGCTGACCACCTGTGCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21828187..21828258 26863196 MeRIP-seq:(Medium) rs368942478 Functional Loss SNV dbSNP153 33..33 33 - - - 63748 RMVar_ID_63748 Human_SNP_ID_5850561 m1A Human chr1 + 21828189 21828189 21828189 GGGCCAGGGCAGAGGCGAGTGGGTGGGTGGGCATGGGCTGGAGGTGTCGCTGACCACCTGTGCCC GGGCCAGGGCAGAGGCGAGTGGGTGGGTGGGCTTGGGCTGGAGGTGTCGCTGACCACCTGTGCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21828187..21828258 26863196 MeRIP-seq:(Medium) rs368942478 Functional Loss SNV dbSNP153 33..33 33 - - - 63749 RMVar_ID_63749 Human_SNP_ID_5851248 m1A Human chr1 + 21830041 21830041 21830041 CCCCGAGCGGCCCAGGTGGCAGCGGCAGGTGTAGCCTCGACCGTCAGGCCGGTTCACACAGGTGG CCCCGAGCGGCCCAGGTGGCAGCGGCAGGTGTGGCCTCGACCGTCAGGCCGGTTCACACAGGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21829976..21830100 32194978 MeRIP-seq:(Medium) rs1235130978 Functional Loss SNV dbSNP153 33..33 33 - - - 63750 RMVar_ID_63750 Human_SNP_ID_5851765 m1A Human chr1 + 21831526 21831526 21831526 GATGGCACCATAGTCAGGATAGCCACCCAGGTAGAGTTCCTCGTTCAGATCCAGGCCCTGGAACT GATGGCACCATAGTCAGGATAGCCACCCAGGTGGAGTTCCTCGTTCAGATCCAGGCCCTGGAACT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21831476..21831550 32194978 MeRIP-seq:(Medium) rs900097165 Functional Loss SNV dbSNP153 33..33 33 - - - 63751 RMVar_ID_63751 Human_SNP_ID_5851934 m1A Human chr1 + 21832044 21832044 21832044 TTCCCAGAGCAGCCCACAGGGACCCCAGGCTCAGCGCCCTGCAGCCTAGCACCTGGCCTCCTTGT TTCCCAGAGCAGCCCACAGGGACCCCAGGCTCCGCGCCCTGCAGCCTAGCACCTGGCCTCCTTGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:21832030..21832138 26863196 MeRIP-seq:(Medium) rs1011308848 Functional Loss SNV dbSNP153 33..33 33 - - - 63752 RMVar_ID_63752 Human_SNP_ID_5852383 m1A Human chr1 - 21833580 21833580 21833580 GGATGGCAGCCTGCCACCTGACAGCCGCCTGGAGAACAACATGCTGATGCTGCCCTCAGTCCGAC GGATGGCAGCCTGCCACCTGACAGCCGCCTGGTGAACAACATGCTGATGCTGCCCTCAGTCCGAC T A HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:21833451..21833600;chr1:21833451..21833625 32194978 MeRIP-seq:(Medium) rs752382140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743016 Human_Splice_Rec_28756,Human_Splice_Rec_28836 Human_miRNA_ID_1935832,Human_miRNA_ID_1946932 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_94946,RMVar_hsa_circ_100643,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_115730,RMVar_hsa_circ_105226,RMVar_hsa_circ_130110,RMVar_hsa_circ_127785,RMVar_hsa_circ_130111,RMVar_hsa_circ_130112,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_99641,RMVar_hsa_circ_130115,RMVar_hsa_circ_130117,RMVar_hsa_circ_79246,RMVar_hsa_circ_130118,RMVar_hsa_circ_130116,RMVar_hsa_circ_130114,RMVar_hsa_circ_85490,RMVar_hsa_circ_96828,RMVar_hsa_circ_103955,RMVar_hsa_circ_124414,RMVar_hsa_circ_130119,RMVar_hsa_circ_130120,RMVar_hsa_circ_101008,RMVar_hsa_circ_105038,RMVar_hsa_circ_130121,RMVar_hsa_circ_130122,RMVar_hsa_circ_122217,RMVar_hsa_circ_114281,RMVar_hsa_circ_130124,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_130125,RMVar_hsa_circ_108451,RMVar_hsa_circ_125375,RMVar_hsa_circ_130128,RMVar_hsa_circ_103599,RMVar_hsa_circ_105034,RMVar_hsa_circ_130129,RMVar_hsa_circ_130131,RMVar_hsa_circ_130130,RMVar_hsa_circ_119540,RMVar_hsa_circ_120925,RMVar_hsa_circ_130134,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130135,RMVar_hsa_circ_130136,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_122487,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_87778,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130145,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_91509,RMVar_hsa_circ_130150,RMVar_hsa_circ_130147,RMVar_hsa_circ_130148,RMVar_hsa_circ_99219,RMVar_hsa_circ_103048,RMVar_hsa_circ_97679,RMVar_hsa_circ_130151,RMVar_hsa_circ_119684,RMVar_hsa_circ_130152,RMVar_hsa_circ_130153,RMVar_hsa_circ_130154,RMVar_hsa_circ_108930,RMVar_hsa_circ_124103,RMVar_hsa_circ_126753,RMVar_hsa_circ_130155,RMVar_hsa_circ_130156,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_115508,RMVar_hsa_circ_117151,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_100297,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_130171,RMVar_hsa_circ_81224,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130175,RMVar_hsa_circ_77424,RMVar_hsa_circ_79303,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130173,RMVar_hsa_circ_130174,RMVar_hsa_circ_130172,RMVar_hsa_circ_130167,RMVar_hsa_circ_130169,RMVar_hsa_circ_130170,RMVar_hsa_circ_130168,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158 63753 RMVar_ID_63753 Human_SNP_ID_5854173 m1A Human chr1 - 21839548 21839548 21839548 ACTTCTGTCATCTTCCACTCGACTCCACAGGCAGCCCCGCGCCCACCATCCACTGGTCCAAGCTG ACTTCTGTCATCTTCCACTCGACTCCACAGGCGGCCCCGCGCCCACCATCCACTGGTCCAAGCTG T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21839376..21839575 32194978 MeRIP-seq:(Medium) rs974133064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_28744 Human_miRNA_ID_1956043,Human_miRNA_ID_2249824,Human_miRNA_ID_2872264,Human_miRNA_ID_2980229,Human_miRNA_ID_3065292 RMVar_hsa_circ_76589,RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_100643,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_115730,RMVar_hsa_circ_105226,RMVar_hsa_circ_130111,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_99641,RMVar_hsa_circ_130115,RMVar_hsa_circ_130117,RMVar_hsa_circ_130116,RMVar_hsa_circ_130114,RMVar_hsa_circ_85490,RMVar_hsa_circ_96828,RMVar_hsa_circ_103955,RMVar_hsa_circ_124414,RMVar_hsa_circ_130119,RMVar_hsa_circ_130120,RMVar_hsa_circ_105038,RMVar_hsa_circ_130122,RMVar_hsa_circ_122217,RMVar_hsa_circ_130124,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_130125,RMVar_hsa_circ_125375,RMVar_hsa_circ_103599,RMVar_hsa_circ_105034,RMVar_hsa_circ_130129,RMVar_hsa_circ_130130,RMVar_hsa_circ_119540,RMVar_hsa_circ_120925,RMVar_hsa_circ_130134,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130135,RMVar_hsa_circ_130136,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_122487,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_87778,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130145,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_91509,RMVar_hsa_circ_130150,RMVar_hsa_circ_130147,RMVar_hsa_circ_130148,RMVar_hsa_circ_99219,RMVar_hsa_circ_97679,RMVar_hsa_circ_130151,RMVar_hsa_circ_130152,RMVar_hsa_circ_108930,RMVar_hsa_circ_124103,RMVar_hsa_circ_126753,RMVar_hsa_circ_130155,RMVar_hsa_circ_130156,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_115508,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_100297,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_130171,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130175,RMVar_hsa_circ_77424,RMVar_hsa_circ_79303,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130173,RMVar_hsa_circ_130174,RMVar_hsa_circ_130172,RMVar_hsa_circ_130167,RMVar_hsa_circ_130170,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_118174,RMVar_hsa_circ_106262,RMVar_hsa_circ_116134,RMVar_hsa_circ_126398,RMVar_hsa_circ_130181,RMVar_hsa_circ_123609,RMVar_hsa_circ_114008,RMVar_hsa_circ_114030,RMVar_hsa_circ_106644,RMVar_hsa_circ_93084,RMVar_hsa_circ_97779,RMVar_hsa_circ_83676,RMVar_hsa_circ_75875,RMVar_hsa_circ_92999,RMVar_hsa_circ_119953,RMVar_hsa_circ_130185,RMVar_hsa_circ_130189,RMVar_hsa_circ_130191,RMVar_hsa_circ_130192,RMVar_hsa_circ_130190,RMVar_hsa_circ_130187,RMVar_hsa_circ_130188,RMVar_hsa_circ_130186,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_81170,RMVar_hsa_circ_118054,RMVar_hsa_circ_130194,RMVar_hsa_circ_130195,RMVar_hsa_circ_125955,RMVar_hsa_circ_337843,RMVar_hsa_circ_113529,RMVar_hsa_circ_124100,RMVar_hsa_circ_130199,RMVar_hsa_circ_130200,RMVar_hsa_circ_370788,RMVar_hsa_circ_334119,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_97766,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_79362,RMVar_hsa_circ_77032,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130214,RMVar_hsa_circ_130216,RMVar_hsa_circ_43665,RMVar_hsa_circ_130217,RMVar_hsa_circ_130215,RMVar_hsa_circ_130212,RMVar_hsa_circ_130213,RMVar_hsa_circ_130211,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_374637,RMVar_hsa_circ_93953,RMVar_hsa_circ_130219,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_130218 63754 RMVar_ID_63754 Human_SNP_ID_5854595 m1A Human chr1 - 21841198 21841198 21841198 GGCTGTCACCCTGGAGTGTGTCAGTGCCGGGGAGCCCCGCTCCTCTGCTCGTTGGACCCGGATCA GGCTGTCACCCTGGAGTGTGTCAGTGCCGGGGGGCCCCGCTCCTCTGCTCGTTGGACCCGGATCA T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21841151..21841300 32194978 MeRIP-seq:(Medium) rs373699453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743022,Human_RBP_ID_3935487,Human_RBP_ID_5233859,Human_RBP_ID_5311575,Human_RBP_ID_5458472,Human_RBP_ID_5518668,Human_RBP_ID_8754818,Human_RBP_ID_18186926,Human_RBP_ID_22429133,Human_RBP_ID_22749902,Human_RBP_ID_23205004,Human_RBP_ID_26767438 Human_Splice_Rec_28740,Human_Splice_Rec_28741 Human_miRNA_ID_2270944,Human_miRNA_ID_3065293 RMVar_hsa_circ_76589,RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_100643,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_115730,RMVar_hsa_circ_105226,RMVar_hsa_circ_130111,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_99641,RMVar_hsa_circ_130115,RMVar_hsa_circ_130117,RMVar_hsa_circ_130116,RMVar_hsa_circ_130114,RMVar_hsa_circ_85490,RMVar_hsa_circ_96828,RMVar_hsa_circ_103955,RMVar_hsa_circ_124414,RMVar_hsa_circ_130119,RMVar_hsa_circ_130120,RMVar_hsa_circ_105038,RMVar_hsa_circ_130122,RMVar_hsa_circ_122217,RMVar_hsa_circ_130124,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_130125,RMVar_hsa_circ_125375,RMVar_hsa_circ_105034,RMVar_hsa_circ_130129,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130136,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_122487,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130145,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_91509,RMVar_hsa_circ_130150,RMVar_hsa_circ_130147,RMVar_hsa_circ_130148,RMVar_hsa_circ_97679,RMVar_hsa_circ_130152,RMVar_hsa_circ_108930,RMVar_hsa_circ_124103,RMVar_hsa_circ_126753,RMVar_hsa_circ_130155,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_115508,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_100297,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_130171,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130175,RMVar_hsa_circ_77424,RMVar_hsa_circ_79303,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130173,RMVar_hsa_circ_130174,RMVar_hsa_circ_130172,RMVar_hsa_circ_130167,RMVar_hsa_circ_130170,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_118174,RMVar_hsa_circ_106262,RMVar_hsa_circ_116134,RMVar_hsa_circ_126398,RMVar_hsa_circ_130181,RMVar_hsa_circ_123609,RMVar_hsa_circ_114008,RMVar_hsa_circ_114030,RMVar_hsa_circ_106644,RMVar_hsa_circ_93084,RMVar_hsa_circ_97779,RMVar_hsa_circ_83676,RMVar_hsa_circ_75875,RMVar_hsa_circ_92999,RMVar_hsa_circ_119953,RMVar_hsa_circ_130185,RMVar_hsa_circ_130189,RMVar_hsa_circ_130191,RMVar_hsa_circ_130192,RMVar_hsa_circ_130190,RMVar_hsa_circ_130187,RMVar_hsa_circ_130188,RMVar_hsa_circ_130186,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_81170,RMVar_hsa_circ_118054,RMVar_hsa_circ_130194,RMVar_hsa_circ_130195,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_124100,RMVar_hsa_circ_130199,RMVar_hsa_circ_130200,RMVar_hsa_circ_370788,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_97766,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_79362,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130214,RMVar_hsa_circ_43665,RMVar_hsa_circ_130215,RMVar_hsa_circ_130212,RMVar_hsa_circ_130213,RMVar_hsa_circ_130211,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_93953,RMVar_hsa_circ_124747,RMVar_hsa_circ_130219,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_111692,RMVar_hsa_circ_118438,RMVar_hsa_circ_130222,RMVar_hsa_circ_130223,RMVar_hsa_circ_130225,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224 63755 RMVar_ID_63755 Human_SNP_ID_5855015 m1A Human chr1 - 21842355 21842355 21842355 CTGACAGACCCATGGCTCCCAGCTGCGGCTCCACCTCGTCTCCCCTGCCGACTCAGGCGAGTATG CTGACAGACCCATGGCTCCCAGCTGCGGCTCCGCCTCGTCTCCCCTGCCGACTCAGGCGAGTATG T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21842226..21842400 26863196 MeRIP-seq:(Medium) rs1020696012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849611 Human_Splice_Rec_28734 RMVar_hsa_circ_76589,RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_100643,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_115730,RMVar_hsa_circ_105226,RMVar_hsa_circ_130111,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_99641,RMVar_hsa_circ_130115,RMVar_hsa_circ_130117,RMVar_hsa_circ_130116,RMVar_hsa_circ_130114,RMVar_hsa_circ_85490,RMVar_hsa_circ_96828,RMVar_hsa_circ_103955,RMVar_hsa_circ_124414,RMVar_hsa_circ_130119,RMVar_hsa_circ_130120,RMVar_hsa_circ_105038,RMVar_hsa_circ_130122,RMVar_hsa_circ_122217,RMVar_hsa_circ_130124,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_130125,RMVar_hsa_circ_125375,RMVar_hsa_circ_105034,RMVar_hsa_circ_130129,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130136,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_122487,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130145,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_91509,RMVar_hsa_circ_130150,RMVar_hsa_circ_130147,RMVar_hsa_circ_130148,RMVar_hsa_circ_97679,RMVar_hsa_circ_130152,RMVar_hsa_circ_108930,RMVar_hsa_circ_124103,RMVar_hsa_circ_126753,RMVar_hsa_circ_130155,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_115508,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_100297,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_130171,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130175,RMVar_hsa_circ_77424,RMVar_hsa_circ_79303,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130173,RMVar_hsa_circ_130174,RMVar_hsa_circ_130172,RMVar_hsa_circ_130167,RMVar_hsa_circ_130170,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_118174,RMVar_hsa_circ_106262,RMVar_hsa_circ_116134,RMVar_hsa_circ_126398,RMVar_hsa_circ_130181,RMVar_hsa_circ_123609,RMVar_hsa_circ_114008,RMVar_hsa_circ_114030,RMVar_hsa_circ_106644,RMVar_hsa_circ_93084,RMVar_hsa_circ_97779,RMVar_hsa_circ_83676,RMVar_hsa_circ_75875,RMVar_hsa_circ_92999,RMVar_hsa_circ_119953,RMVar_hsa_circ_130185,RMVar_hsa_circ_130189,RMVar_hsa_circ_130191,RMVar_hsa_circ_130192,RMVar_hsa_circ_130190,RMVar_hsa_circ_130187,RMVar_hsa_circ_130188,RMVar_hsa_circ_130186,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_81170,RMVar_hsa_circ_118054,RMVar_hsa_circ_130194,RMVar_hsa_circ_130195,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_124100,RMVar_hsa_circ_130199,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_97766,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_79362,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130214,RMVar_hsa_circ_43665,RMVar_hsa_circ_130212,RMVar_hsa_circ_130213,RMVar_hsa_circ_130211,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_93953,RMVar_hsa_circ_124747,RMVar_hsa_circ_130219,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_111692,RMVar_hsa_circ_118438,RMVar_hsa_circ_130222,RMVar_hsa_circ_130223,RMVar_hsa_circ_130225,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_372522,RMVar_hsa_circ_374252,RMVar_hsa_circ_119604,RMVar_hsa_circ_126678,RMVar_hsa_circ_130226,RMVar_hsa_circ_76103,RMVar_hsa_circ_103838,RMVar_hsa_circ_130228,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_130227,RMVar_hsa_circ_127595,RMVar_hsa_circ_128121,RMVar_hsa_circ_362428,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130237,RMVar_hsa_circ_103099,RMVar_hsa_circ_130238,RMVar_hsa_circ_130236,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_130239 63756 RMVar_ID_63756 Human_SNP_ID_5855016 m1A Human chr1 - 21842355 21842355 21842355 CTGACAGACCCATGGCTCCCAGCTGCGGCTCCACCTCGTCTCCCCTGCCGACTCAGGCGAGTATG CTGACAGACCCATGGCTCCCAGCTGCGGCTCCCCCTCGTCTCCCCTGCCGACTCAGGCGAGTATG T G HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21842226..21842400 26863196 MeRIP-seq:(Medium) rs1020696012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849611 Human_Splice_Rec_28734 RMVar_hsa_circ_76589,RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_100643,RMVar_hsa_circ_130108,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_115730,RMVar_hsa_circ_105226,RMVar_hsa_circ_130111,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_99641,RMVar_hsa_circ_130115,RMVar_hsa_circ_130117,RMVar_hsa_circ_130116,RMVar_hsa_circ_130114,RMVar_hsa_circ_85490,RMVar_hsa_circ_96828,RMVar_hsa_circ_103955,RMVar_hsa_circ_124414,RMVar_hsa_circ_130119,RMVar_hsa_circ_130120,RMVar_hsa_circ_105038,RMVar_hsa_circ_130122,RMVar_hsa_circ_122217,RMVar_hsa_circ_130124,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_130125,RMVar_hsa_circ_125375,RMVar_hsa_circ_105034,RMVar_hsa_circ_130129,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130136,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_122487,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130145,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_91509,RMVar_hsa_circ_130150,RMVar_hsa_circ_130147,RMVar_hsa_circ_130148,RMVar_hsa_circ_97679,RMVar_hsa_circ_130152,RMVar_hsa_circ_108930,RMVar_hsa_circ_124103,RMVar_hsa_circ_126753,RMVar_hsa_circ_130155,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_115508,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_100297,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_130171,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130175,RMVar_hsa_circ_77424,RMVar_hsa_circ_79303,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130173,RMVar_hsa_circ_130174,RMVar_hsa_circ_130172,RMVar_hsa_circ_130167,RMVar_hsa_circ_130170,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_118174,RMVar_hsa_circ_106262,RMVar_hsa_circ_116134,RMVar_hsa_circ_126398,RMVar_hsa_circ_130181,RMVar_hsa_circ_123609,RMVar_hsa_circ_114008,RMVar_hsa_circ_114030,RMVar_hsa_circ_106644,RMVar_hsa_circ_93084,RMVar_hsa_circ_97779,RMVar_hsa_circ_83676,RMVar_hsa_circ_75875,RMVar_hsa_circ_92999,RMVar_hsa_circ_119953,RMVar_hsa_circ_130185,RMVar_hsa_circ_130189,RMVar_hsa_circ_130191,RMVar_hsa_circ_130192,RMVar_hsa_circ_130190,RMVar_hsa_circ_130187,RMVar_hsa_circ_130188,RMVar_hsa_circ_130186,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_81170,RMVar_hsa_circ_118054,RMVar_hsa_circ_130194,RMVar_hsa_circ_130195,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_124100,RMVar_hsa_circ_130199,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_97766,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_79362,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130214,RMVar_hsa_circ_43665,RMVar_hsa_circ_130212,RMVar_hsa_circ_130213,RMVar_hsa_circ_130211,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_93953,RMVar_hsa_circ_124747,RMVar_hsa_circ_130219,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_111692,RMVar_hsa_circ_118438,RMVar_hsa_circ_130222,RMVar_hsa_circ_130223,RMVar_hsa_circ_130225,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_372522,RMVar_hsa_circ_374252,RMVar_hsa_circ_119604,RMVar_hsa_circ_126678,RMVar_hsa_circ_130226,RMVar_hsa_circ_76103,RMVar_hsa_circ_103838,RMVar_hsa_circ_130228,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_130227,RMVar_hsa_circ_127595,RMVar_hsa_circ_128121,RMVar_hsa_circ_362428,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130237,RMVar_hsa_circ_103099,RMVar_hsa_circ_130238,RMVar_hsa_circ_130236,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_130239 63757 RMVar_ID_63757 Human_SNP_ID_5856462 m1A Human chr1 + 21847384 21847384 21847384 ACCGGAGGGGCTGCCGGCGCTAGGGGAGACGGAGATGACGATGGAGGCCTCCAGGGCATCGATGT ACCGGAGGGGCTGCCGGCGCTAGGGGAGACGGGGATGACGATGGAGGCCTCCAGGGCATCGATGT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21847351..21847475 26863196 MeRIP-seq:(Medium) rs1431064525 Functional Loss SNV dbSNP153 33..33 33 - - - 63758 RMVar_ID_63758 Human_SNP_ID_5857076 m1A Human chr1 + 21848977 21848977 21848977 GGTACCTGAGCTGCCGACCACACGGCACACGTACTCCCCTGAATCAGCTGGGGTCACCTGGAGCA GGTACCTGAGCTGCCGACCACACGGCACACGTTCTCCCCTGAATCAGCTGGGGTCACCTGGAGCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21848926..21849025 32194978 MeRIP-seq:(Medium) rs763357907 Functional Loss SNV dbSNP153 33..33 33 - - - 63759 RMVar_ID_63759 Human_SNP_ID_5858295 m1A Human chr1 - 21852777 21852777 21852777 GCACCAGGTGACCCCGGCCGACTCAGGCGAGTATGTGTGCCATGTGGTGGGCACCTCCGGCCCCC GCACCAGGTGACCCCGGCCGACTCAGGCGAGTGTGTGTGCCATGTGGTGGGCACCTCCGGCCCCC T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21852726..21852800 32194978 MeRIP-seq:(Medium) rs915302866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18415934 Human_Splice_Rec_28702,Human_Splice_Rec_28703 Human_miRNA_ID_2133292 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_122217,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_128109,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130144,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_86594,RMVar_hsa_circ_83528,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130176,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_116134,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_106644,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130187,RMVar_hsa_circ_130186,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_97766,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130211,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_103099,RMVar_hsa_circ_130236,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_130239,RMVar_hsa_circ_83653,RMVar_hsa_circ_89586,RMVar_hsa_circ_130244,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_94899,RMVar_hsa_circ_130253,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_77227,RMVar_hsa_circ_25582,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_267451,RMVar_hsa_circ_90336,RMVar_hsa_circ_89467,RMVar_hsa_circ_108295,RMVar_hsa_circ_130262,RMVar_hsa_circ_130264,RMVar_hsa_circ_130263,RMVar_hsa_circ_124789,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130267,RMVar_hsa_circ_130269,RMVar_hsa_circ_130270,RMVar_hsa_circ_130268,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_357409,RMVar_hsa_circ_111140,RMVar_hsa_circ_83228,RMVar_hsa_circ_125663,RMVar_hsa_circ_130276,RMVar_hsa_circ_361563,RMVar_hsa_circ_130277,RMVar_hsa_circ_130279,RMVar_hsa_circ_80400,RMVar_hsa_circ_130278,RMVar_hsa_circ_126853,RMVar_hsa_circ_375768,RMVar_hsa_circ_130280,RMVar_hsa_circ_130281,RMVar_hsa_circ_130282 63760 RMVar_ID_63760 Human_SNP_ID_5859055 m1A Human chr1 + 21854829 21854829 21854829 GGGGAGCCCTGGCTTGCCCTCCCCACCCCTCCATTCCCAGAGAGTCCGTACCTGAAAGGACAACC GGGGAGCCCTGGCTTGCCCTCCCCACCCCTCCGTTCCCAGAGAGTCCGTACCTGAAAGGACAACC A G HSALNG0001536 RNACentral:URS0000EBCAC7 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21854826..21854900 32194978 MeRIP-seq:(Medium) rs36080251 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_239,Clinvar_Rec_240,Clinvar_Rec_241,Clinvar_Rec_242,Clinvar_Rec_243,Clinvar_Rec_244,Clinvar_Rec_245 63761 RMVar_ID_63761 Human_SNP_ID_5859122 m1A Human chr1 - 21854975 21854975 21854975 GCTGACCCATCTCACCCACGGCAGGCCCGGTCAGAGCGCACAGACATCGCGACACTGCTCATCCC GCTGACCCATCTCACCCACGGCAGGCCCGGTCGGAGCGCACAGACATCGCGACACTGCTCATCCC T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21854926..21854975 32194978 MeRIP-seq:(Medium) rs984699512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_97383 Human_Splice_Rec_28694 Human_miRNA_ID_2978097 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_122217,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_83528,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_108132,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130210,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_77800,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130220,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_130239,RMVar_hsa_circ_89586,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_267451,RMVar_hsa_circ_90336,RMVar_hsa_circ_108295,RMVar_hsa_circ_130262,RMVar_hsa_circ_130263,RMVar_hsa_circ_124789,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130269,RMVar_hsa_circ_130270,RMVar_hsa_circ_130268,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_12085,RMVar_hsa_circ_111140,RMVar_hsa_circ_83228,RMVar_hsa_circ_125663,RMVar_hsa_circ_130276,RMVar_hsa_circ_130277,RMVar_hsa_circ_80400,RMVar_hsa_circ_130278,RMVar_hsa_circ_126853,RMVar_hsa_circ_130283,RMVar_hsa_circ_130281,RMVar_hsa_circ_130282,RMVar_hsa_circ_108100,RMVar_hsa_circ_101611,RMVar_hsa_circ_375034,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_107286,RMVar_hsa_circ_130285,RMVar_hsa_circ_130286,RMVar_hsa_circ_130284,RMVar_hsa_circ_95979,RMVar_hsa_circ_100811,RMVar_hsa_circ_130288,RMVar_hsa_circ_130289,RMVar_hsa_circ_130287,RMVar_hsa_circ_130290 63762 RMVar_ID_63762 Human_SNP_ID_5859506 m1A Human chr1 - 21855802 21855802 21855802 TCCGCTGCAGCGCCACAGGGAGCCCCACGCCCACCCTCGAGTGGACAGGTGAGGCCGTGATGGGA TCCGCTGCAGCGCCACAGGGAGCCCCACGCCCGCCCTCGAGTGGACAGGTGAGGCCGTGATGGGA T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21855801..21855850 32194978 MeRIP-seq:(Medium) rs1192648239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22749914 Human_Splice_Rec_28689 Human_miRNA_ID_2872266,Human_miRNA_ID_2980231 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_122217,RMVar_hsa_circ_130126,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_94345,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_83528,RMVar_hsa_circ_130177,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130178,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_130239,RMVar_hsa_circ_85332,RMVar_hsa_circ_89586,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_267451,RMVar_hsa_circ_90336,RMVar_hsa_circ_130262,RMVar_hsa_circ_130263,RMVar_hsa_circ_124789,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130269,RMVar_hsa_circ_130270,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_12085,RMVar_hsa_circ_111140,RMVar_hsa_circ_125663,RMVar_hsa_circ_130276,RMVar_hsa_circ_126853,RMVar_hsa_circ_130283,RMVar_hsa_circ_130281,RMVar_hsa_circ_130282,RMVar_hsa_circ_108100,RMVar_hsa_circ_101611,RMVar_hsa_circ_375034,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_107286,RMVar_hsa_circ_130285,RMVar_hsa_circ_130286,RMVar_hsa_circ_130284,RMVar_hsa_circ_95979,RMVar_hsa_circ_100811,RMVar_hsa_circ_130288,RMVar_hsa_circ_130289,RMVar_hsa_circ_130287,RMVar_hsa_circ_112020,RMVar_hsa_circ_130290,RMVar_hsa_circ_130291,RMVar_hsa_circ_130292 63763 RMVar_ID_63763 Human_SNP_ID_5859855 m1A Human chr1 + 21856983 21856978 21856984 GCTAATTCTGGTGGGAATGGGGGAGAGACAGGAGGGGAGAATCAGGTATAGATGGGAGGTGTACC GCTAATTCTGGTGGGAATGGGGGAGAGCCAGGGTGGGAGAATCAGGTATAGATGGGAGGTGTACC ACAGGAG CCAGGGT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21856980..21857097 26863196 MeRIP-seq:(Medium) rs71589744 Functional Loss MNV dbSNP153 28..34 33 - - - 63764 RMVar_ID_63764 Human_SNP_ID_5859860 m1A Human chr1 + 21856983 21856983 21856984 GCTAATTCTGGTGGGAATGGGGGAGAGACAGGAGGGGAGAATCAGGTATAGATGGGAGGTGTACC GCTAATTCTGGTGGGAATGGGGGAGAGACAGGGTGGGAGAATCAGGTATAGATGGGAGGTGTACC AG GT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21856980..21857097 26863196 MeRIP-seq:(Medium) rs386629396 Functional Loss MNV dbSNP153 33..34 33 - - - 63765 RMVar_ID_63765 Human_SNP_ID_5859862 m1A Human chr1 + 21856983 21856983 21856983 GCTAATTCTGGTGGGAATGGGGGAGAGACAGGAGGGGAGAATCAGGTATAGATGGGAGGTGTACC GCTAATTCTGGTGGGAATGGGGGAGAGACAGGCGGGGAGAATCAGGTATAGATGGGAGGTGTACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21856980..21857097 26863196 MeRIP-seq:(Medium) rs200354565 Functional Loss SNV dbSNP153 33..33 33 - - - 63766 RMVar_ID_63766 Human_SNP_ID_5859863 m1A Human chr1 + 21856983 21856983 21856983 GCTAATTCTGGTGGGAATGGGGGAGAGACAGGAGGGGAGAATCAGGTATAGATGGGAGGTGTACC GCTAATTCTGGTGGGAATGGGGGAGAGACAGGGGGGGAGAATCAGGTATAGATGGGAGGTGTACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21856980..21857097 26863196 MeRIP-seq:(Medium) rs200354565 Functional Loss SNV dbSNP153 33..33 33 - - - 63767 RMVar_ID_63767 Human_SNP_ID_5860005 m1A Human chr1 + 21857331 21857331 21857331 TGCAGATGAAGGTGACGTCAGCTCCGGGGCGCACGCTCTGGCTCCGCTGCTCCTCCACAGTCACT TGCAGATGAAGGTGACGTCAGCTCCGGGGCGCGCGCTCTGGCTCCGCTGCTCCTCCACAGTCACT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21857326..21857350 26863196 MeRIP-seq:(Medium) rs1031570794 Functional Loss SNV dbSNP153 33..33 33 - - - 63768 RMVar_ID_63768 Human_SNP_ID_5860586 m1A Human chr1 - 21859626 21859626 21859626 CCAGCGTCCAGCCCTCGGATGCTGGGGTCTACATTTGCACCTGCCGTAATCTCCACCAATCCAAT CCAGCGTCCAGCCCTCGGATGCTGGGGTCTACTTTTGCACCTGCCGTAATCTCCACCAATCCAAT T A HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21859576..21859700 26863196 MeRIP-seq:(Medium) rs755648738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_28682,Human_Splice_Rec_28683 Human_miRNA_ID_1983641,Human_miRNA_ID_2179673,Human_miRNA_ID_2181778 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_130239,RMVar_hsa_circ_85332,RMVar_hsa_circ_89586,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_267451,RMVar_hsa_circ_90336,RMVar_hsa_circ_130262,RMVar_hsa_circ_130263,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130270,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_12085,RMVar_hsa_circ_111140,RMVar_hsa_circ_125663,RMVar_hsa_circ_130276,RMVar_hsa_circ_130283,RMVar_hsa_circ_130282,RMVar_hsa_circ_108100,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_107286,RMVar_hsa_circ_130286,RMVar_hsa_circ_95979,RMVar_hsa_circ_100811,RMVar_hsa_circ_130288,RMVar_hsa_circ_130289,RMVar_hsa_circ_130287,RMVar_hsa_circ_112020,RMVar_hsa_circ_130290,RMVar_hsa_circ_32512,RMVar_hsa_circ_109886,RMVar_hsa_circ_104450,RMVar_hsa_circ_130291,RMVar_hsa_circ_130292,RMVar_hsa_circ_108026,RMVar_hsa_circ_130293,RMVar_hsa_circ_130294,RMVar_hsa_circ_127671,RMVar_hsa_circ_130296,RMVar_hsa_circ_105126,RMVar_hsa_circ_105497,RMVar_hsa_circ_130297,RMVar_hsa_circ_130298,RMVar_hsa_circ_124401,RMVar_hsa_circ_130295,RMVar_hsa_circ_81313,RMVar_hsa_circ_130299,RMVar_hsa_circ_130300 63769 RMVar_ID_63769 Human_SNP_ID_5860587 m1A Human chr1 - 21859626 21859626 21859626 CCAGCGTCCAGCCCTCGGATGCTGGGGTCTACATTTGCACCTGCCGTAATCTCCACCAATCCAAT CCAGCGTCCAGCCCTCGGATGCTGGGGTCTACCTTTGCACCTGCCGTAATCTCCACCAATCCAAT T G HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21859576..21859700 26863196 MeRIP-seq:(Medium) rs755648738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_28682,Human_Splice_Rec_28683 Human_miRNA_ID_1983641,Human_miRNA_ID_2179673,Human_miRNA_ID_2181778 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_78646,RMVar_hsa_circ_130235,RMVar_hsa_circ_111349,RMVar_hsa_circ_123757,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_130239,RMVar_hsa_circ_85332,RMVar_hsa_circ_89586,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_267451,RMVar_hsa_circ_90336,RMVar_hsa_circ_130262,RMVar_hsa_circ_130263,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130270,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_12085,RMVar_hsa_circ_111140,RMVar_hsa_circ_125663,RMVar_hsa_circ_130276,RMVar_hsa_circ_130283,RMVar_hsa_circ_130282,RMVar_hsa_circ_108100,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_107286,RMVar_hsa_circ_130286,RMVar_hsa_circ_95979,RMVar_hsa_circ_100811,RMVar_hsa_circ_130288,RMVar_hsa_circ_130289,RMVar_hsa_circ_130287,RMVar_hsa_circ_112020,RMVar_hsa_circ_130290,RMVar_hsa_circ_32512,RMVar_hsa_circ_109886,RMVar_hsa_circ_104450,RMVar_hsa_circ_130291,RMVar_hsa_circ_130292,RMVar_hsa_circ_108026,RMVar_hsa_circ_130293,RMVar_hsa_circ_130294,RMVar_hsa_circ_127671,RMVar_hsa_circ_130296,RMVar_hsa_circ_105126,RMVar_hsa_circ_105497,RMVar_hsa_circ_130297,RMVar_hsa_circ_130298,RMVar_hsa_circ_124401,RMVar_hsa_circ_130295,RMVar_hsa_circ_81313,RMVar_hsa_circ_130299,RMVar_hsa_circ_130300 63770 RMVar_ID_63770 Human_SNP_ID_5860837 m1A Human chr1 - 21860226 21860226 21860226 CCGGCCCTTGTTCCCCCTTACAGGTGTGGCCCAGGTTACGTGGGTAACCCCAGTGTGCAAGGGGG CCGGCCCTTGTTCCCCCTTACAGGTGTGGCCCGGGTTACGTGGGTAACCCCAGTGTGCAAGGGGG T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21860176..21860250 32194978 MeRIP-seq:(Medium) rs1160187920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222098,Human_RBP_ID_3935498,Human_RBP_ID_5519708,Human_RBP_ID_22426981,Human_RBP_ID_22748947 Human_Splice_Rec_28678,Human_Splice_Rec_28679 Human_miRNA_ID_2581983,Human_miRNA_ID_2722954 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_84471,RMVar_hsa_circ_130109,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_77609,RMVar_hsa_circ_130127,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_90712,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_125664,RMVar_hsa_circ_130141,RMVar_hsa_circ_130143,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_130149,RMVar_hsa_circ_95063,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_130148,RMVar_hsa_circ_127734,RMVar_hsa_circ_126422,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_130179,RMVar_hsa_circ_75960,RMVar_hsa_circ_130167,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_125955,RMVar_hsa_circ_113529,RMVar_hsa_circ_130200,RMVar_hsa_circ_122146,RMVar_hsa_circ_103641,RMVar_hsa_circ_82643,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_85537,RMVar_hsa_circ_79093,RMVar_hsa_circ_109894,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130208,RMVar_hsa_circ_130209,RMVar_hsa_circ_130207,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_103838,RMVar_hsa_circ_130230,RMVar_hsa_circ_130231,RMVar_hsa_circ_130229,RMVar_hsa_circ_128121,RMVar_hsa_circ_127400,RMVar_hsa_circ_123757,RMVar_hsa_circ_130233,RMVar_hsa_circ_130234,RMVar_hsa_circ_130232,RMVar_hsa_circ_93305,RMVar_hsa_circ_85332,RMVar_hsa_circ_89586,RMVar_hsa_circ_130245,RMVar_hsa_circ_85524,RMVar_hsa_circ_130248,RMVar_hsa_circ_130247,RMVar_hsa_circ_116158,RMVar_hsa_circ_130258,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_90336,RMVar_hsa_circ_130262,RMVar_hsa_circ_130263,RMVar_hsa_circ_103279,RMVar_hsa_circ_109266,RMVar_hsa_circ_130270,RMVar_hsa_circ_87844,RMVar_hsa_circ_130272,RMVar_hsa_circ_130273,RMVar_hsa_circ_12085,RMVar_hsa_circ_111140,RMVar_hsa_circ_130283,RMVar_hsa_circ_130282,RMVar_hsa_circ_108100,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_107286,RMVar_hsa_circ_130286,RMVar_hsa_circ_100811,RMVar_hsa_circ_130288,RMVar_hsa_circ_130289,RMVar_hsa_circ_112020,RMVar_hsa_circ_130290,RMVar_hsa_circ_32512,RMVar_hsa_circ_109886,RMVar_hsa_circ_104450,RMVar_hsa_circ_130291,RMVar_hsa_circ_130292,RMVar_hsa_circ_108026,RMVar_hsa_circ_130293,RMVar_hsa_circ_130294,RMVar_hsa_circ_127671,RMVar_hsa_circ_130296,RMVar_hsa_circ_105126,RMVar_hsa_circ_105497,RMVar_hsa_circ_130297,RMVar_hsa_circ_130298,RMVar_hsa_circ_124401,RMVar_hsa_circ_130295,RMVar_hsa_circ_81313,RMVar_hsa_circ_95249,RMVar_hsa_circ_127506,RMVar_hsa_circ_130299,RMVar_hsa_circ_130300,RMVar_hsa_circ_117100,RMVar_hsa_circ_130301,RMVar_hsa_circ_111690,RMVar_hsa_circ_130303,RMVar_hsa_circ_130304,RMVar_hsa_circ_130302 63771 RMVar_ID_63771 Human_SNP_ID_5864285 m1A Human chr1 + 21872374 21872373 21872374 GCCTTGGAAGTCCCCAGGGGCAAAGTGGGTGGAGATCTGGCAGGGGAAAAAGGAGGGGGCGTCAG GCCTTGGAAGTCCCCAGGGGCAAAGTGGGTGG_GATCTGGCAGGGGAAAAAGGAGGGGGCGTCAG GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:21872351..21872375 26863196 MeRIP-seq:(Medium) rs34397328 Functional Loss DEL dbSNP153 33..33 33 - - - 63772 RMVar_ID_63772 Human_SNP_ID_5864287 m1A Human chr1 + 21872374 21872374 21872374 GCCTTGGAAGTCCCCAGGGGCAAAGTGGGTGGAGATCTGGCAGGGGAAAAAGGAGGGGGCGTCAG GCCTTGGAAGTCCCCAGGGGCAAAGTGGGTGGCGATCTGGCAGGGGAAAAAGGAGGGGGCGTCAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:21872351..21872375 26863196 MeRIP-seq:(Medium) rs773611162 Functional Loss SNV dbSNP153 33..33 33 - - - 63773 RMVar_ID_63773 Human_SNP_ID_5867570 m1A Human chr1 + 21881445 21881445 21881445 GCTGGAACTCGTGCAGGGATGGGTCGATCTGCAGCTGCGTGGAGGAGAGGGGTGGCGTGCCGGGC GCTGGAACTCGTGCAGGGATGGGTCGATCTGCCGCTGCGTGGAGGAGAGGGGTGGCGTGCCGGGC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21881426..21881450 26863196 MeRIP-seq:(Medium) rs1367776431 Functional Loss SNV dbSNP153 33..33 33 - - - 63774 RMVar_ID_63774 Human_SNP_ID_5867595 m1A Human chr1 - 21881488 21881488 21881488 CCCCCTTGCCACCCACAGGTGTGAATGTGACAATGCCTGCGCAGCCCGGCACGCCACCCCTCTCC CCCCCTTGCCACCCACAGGTGTGAATGTGACAGTGCCTGCGCAGCCCGGCACGCCACCCCTCTCC T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:21881437..21881545 26863196 MeRIP-seq:(Medium) rs1557776811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3933025,Human_RBP_ID_18186956,Human_RBP_ID_22531924 Human_Splice_Rec_28626 RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_130114,RMVar_hsa_circ_107661,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_79396,RMVar_hsa_circ_130141,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_127734,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_130159,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_130183,RMVar_hsa_circ_130182,RMVar_hsa_circ_88033,RMVar_hsa_circ_79093,RMVar_hsa_circ_130202,RMVar_hsa_circ_130201,RMVar_hsa_circ_119604,RMVar_hsa_circ_130231,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_130261,RMVar_hsa_circ_109266,RMVar_hsa_circ_130273,RMVar_hsa_circ_99848,RMVar_hsa_circ_130286,RMVar_hsa_circ_127671,RMVar_hsa_circ_105126,RMVar_hsa_circ_130297,RMVar_hsa_circ_130298,RMVar_hsa_circ_127506,RMVar_hsa_circ_130302,RMVar_hsa_circ_112358,RMVar_hsa_circ_115274,RMVar_hsa_circ_130309,RMVar_hsa_circ_130310,RMVar_hsa_circ_116992,RMVar_hsa_circ_130312,RMVar_hsa_circ_97024,RMVar_hsa_circ_130314,RMVar_hsa_circ_104140,RMVar_hsa_circ_102017,RMVar_hsa_circ_106377,RMVar_hsa_circ_130315,RMVar_hsa_circ_130316,RMVar_hsa_circ_115015,RMVar_hsa_circ_104207,RMVar_hsa_circ_89670,RMVar_hsa_circ_130319,RMVar_hsa_circ_130320,RMVar_hsa_circ_130321,RMVar_hsa_circ_130324,RMVar_hsa_circ_130326,RMVar_hsa_circ_95647,RMVar_hsa_circ_109710,RMVar_hsa_circ_83874,RMVar_hsa_circ_15814,RMVar_hsa_circ_130328,RMVar_hsa_circ_130329,RMVar_hsa_circ_126790,RMVar_hsa_circ_130332,RMVar_hsa_circ_345328,RMVar_hsa_circ_130334,RMVar_hsa_circ_130338,RMVar_hsa_circ_114096,RMVar_hsa_circ_123763,RMVar_hsa_circ_124762,RMVar_hsa_circ_121542,RMVar_hsa_circ_104762,RMVar_hsa_circ_130339,RMVar_hsa_circ_130336,RMVar_hsa_circ_130337,RMVar_hsa_circ_130340,RMVar_hsa_circ_130335,RMVar_hsa_circ_291448 63775 RMVar_ID_63775 Human_SNP_ID_5868570 m1A Human chr1 + 21885050 21885050 21885050 ATGAGAGGGGATGTGGCCCCAGTTGAGCCTCCAATTGATGATGGGGGTGGGGACGCCAATGGCCA ATGAGAGGGGATGTGGCCCCAGTTGAGCCTCCCATTGATGATGGGGGTGGGGACGCCAATGGCCA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:21885026..21885100 26863196 MeRIP-seq:(Medium) rs902023310 Functional Loss SNV dbSNP153 33..33 33 - - - 63776 RMVar_ID_63776 Human_SNP_ID_5869397 m1A Human chr1 - 21887537 21887537 21887537 ACGCTCCTCAGCCCCTGCTTCCCGGTTCCGTCAGGCCCCTGCCCTGTGGGCCCCAGGAGGCCGCA ACGCTCCTCAGCCCCTGCTTCCCGGTTCCGTCCGGCCCCTGCCCTGTGGGCCCCAGGAGGCCGCA T G HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21887401..21887675 32194978 MeRIP-seq:(Medium) rs1291085909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3935525,Human_RBP_ID_22428203 RMVar_hsa_circ_77542,RMVar_hsa_circ_130138,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_119604,RMVar_hsa_circ_130231,RMVar_hsa_circ_87462,RMVar_hsa_circ_130261,RMVar_hsa_circ_102017,RMVar_hsa_circ_106377,RMVar_hsa_circ_130315,RMVar_hsa_circ_130316,RMVar_hsa_circ_104207,RMVar_hsa_circ_89670,RMVar_hsa_circ_130321,RMVar_hsa_circ_130324,RMVar_hsa_circ_130326,RMVar_hsa_circ_95647,RMVar_hsa_circ_109710,RMVar_hsa_circ_53045,RMVar_hsa_circ_15814,RMVar_hsa_circ_130328,RMVar_hsa_circ_126790,RMVar_hsa_circ_130332,RMVar_hsa_circ_130338,RMVar_hsa_circ_114096,RMVar_hsa_circ_121542,RMVar_hsa_circ_104762,RMVar_hsa_circ_130339,RMVar_hsa_circ_130337,RMVar_hsa_circ_2961,RMVar_hsa_circ_116722,RMVar_hsa_circ_267037,RMVar_hsa_circ_118308,RMVar_hsa_circ_130343,RMVar_hsa_circ_130344,RMVar_hsa_circ_114845,RMVar_hsa_circ_130347 63777 RMVar_ID_63777 Human_SNP_ID_5871866 m1A Human chr1 - 21896303 21896303 21896303 TCAATCAGCTCTCGTTTGCTTACAGGTGACCCATGGGCTGAGGGCATACGATGGCTTGTCTCTGC TCAATCAGCTCTCGTTTGCTTACAGGTGACCCGTGGGCTGAGGGCATACGATGGCTTGTCTCTGC T C HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:21896276..21896407;chr1:21896176..21896371 26863196 MeRIP-seq:(Medium) rs756143996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743061,Human_RBP_ID_859724,Human_RBP_ID_3933048,Human_RBP_ID_4025853,Human_RBP_ID_5312366,Human_RBP_ID_8939952,Human_RBP_ID_18967571 Human_Splice_Rec_28602 RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_126790,RMVar_hsa_circ_130332,RMVar_hsa_circ_121542,RMVar_hsa_circ_130339,RMVar_hsa_circ_98883,RMVar_hsa_circ_130350,RMVar_hsa_circ_83073,RMVar_hsa_circ_92491,RMVar_hsa_circ_130353,RMVar_hsa_circ_130352,RMVar_hsa_circ_130354,RMVar_hsa_circ_376108 63778 RMVar_ID_63778 Human_SNP_ID_5871869 m1A Human chr1 - 21896312 21896312 21896312 GAGAGTGACTCAATCAGCTCTCGTTTGCTTACAGGTGACCCATGGGCTGAGGGCATACGATGGCT GAGAGTGACTCAATCAGCTCTCGTTTGCTTACGGGTGACCCATGGGCTGAGGGCATACGATGGCT T C HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr1:21896291..21896404;chr1:21896276..21896424 26863196 MeRIP-seq:(Medium) rs1165605313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96196,RMVar_hsa_circ_130157,RMVar_hsa_circ_121542,RMVar_hsa_circ_130339,RMVar_hsa_circ_83073,RMVar_hsa_circ_130353 63779 RMVar_ID_63779 Human_SNP_ID_5874099 m1A Human chr1 + 21905317 21905316 21905317 CGCTCCAACCTCTTTTGCTACTGTGCTCCCCCAACTCCCTGCCTTCTAAAATAGCCACATGCATC CGCTCCAACCTCTTTTGCTACTGTGCTCCCCC_ACTCCCTGCCTTCTAAAATAGCCACATGCATC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21905312..21905416 26863196 MeRIP-seq:(Medium) rs911361787 Functional Loss DEL dbSNP153 33..33 33 - - - 63780 RMVar_ID_63780 Human_SNP_ID_5876453 m1A Human chr1 + 21914890 21914890 21914890 AACTGCCCAGAGCAACCACCTGCCTGACCCCCAAAAGCTCACATCCTGCCTATGCCTGCCTGGGC AACTGCCCAGAGCAACCACCTGCCTGACCCCCCAAAGCTCACATCCTGCCTATGCCTGCCTGGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21914887..21915011 26863196 MeRIP-seq:(Medium) rs927943669 Functional Loss SNV dbSNP153 33..33 33 - - - 63781 RMVar_ID_63781 Human_SNP_ID_5876454 m1A Human chr1 + 21914890 21914890 21914890 AACTGCCCAGAGCAACCACCTGCCTGACCCCCAAAAGCTCACATCCTGCCTATGCCTGCCTGGGC AACTGCCCAGAGCAACCACCTGCCTGACCCCCGAAAGCTCACATCCTGCCTATGCCTGCCTGGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21914887..21915011 26863196 MeRIP-seq:(Medium) rs927943669 Functional Loss SNV dbSNP153 33..33 33 - - - 63782 RMVar_ID_63782 Human_SNP_ID_5880336 m1A Human chr1 + 21929690 21929686 21929690 GTTCTGAGAATTCTGGACTCCACCTCCTGCCCACTCCTCCTGGAACTTTCCCATCTCAGGTAGTG GTTCTGAGAATTCTGGACTCCACCTCCTG____CTCCTCCTGGAACTTTCCCATCTCAGGTAGTG GCCCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:21929686..21929785 26863196 MeRIP-seq:(Medium) rs1266296045 Functional Loss DEL dbSNP153 30..33 33 - - - 63783 RMVar_ID_63783 Human_SNP_ID_5882282 m1A Human chr1 - 21936849 21936849 21936849 GTGCTGGAGTCTCGCTGGGCATGGTCCGGCCTACCATTCCTGGGGACCAGGAGGGGAAACTTTGA GTGCTGGAGTCTCGCTGGGCATGGTCCGGCCTGCCATTCCTGGGGACCAGGAGGGGAAACTTTGA T C HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:21936847..21937079 26863196 MeRIP-seq:(Medium) rs912962125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5136120,Human_RBP_ID_5311580,Human_RBP_ID_8052510,Human_RBP_ID_18455538,Human_RBP_ID_18473795,Human_RBP_ID_23365554 RMVar_hsa_circ_96196,RMVar_hsa_circ_130157,RMVar_hsa_circ_121542,RMVar_hsa_circ_130339,RMVar_hsa_circ_83073,RMVar_hsa_circ_130353 63784 RMVar_ID_63784 Human_SNP_ID_5909381 m1A Human chr1 + 22030736 22030736 22030736 GCTCAAGCACAGAGATGTCAGCCTGGAATCAGAATCACTGGCTAAGTCTTGCTGCTTGCTTCTTG GCTCAAGCACAGAGATGTCAGCCTGGAATCAGTATCACTGGCTAAGTCTTGCTGCTTGCTTCTTG A T AL031281.1,LINC00339,CDC42 Ensembl:ENSG00000285794,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 Pseudogene,lincRNA,Protein coding exon,exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3820687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8242546,Human_RBP_ID_17765458,Human_RBP_ID_26797864 GWAS_ID_7755 63785 RMVar_ID_63785 Human_SNP_ID_5915293 m1A Human chr1 - 22052739 22052739 22052739 CCGCGGGGAACCTCGGGCCCCGCACTCACCTCAGCTTCTCCACCGGGGCGTTGGCAGCACTGCGC CCGCGGGGAACCTCGGGCCCCGCACTCACCTCGGCTTCTCCACCGGGGCGTTGGCAGCACTGCGC T C CDC42-AS1 Ensembl:ENSG00000285752 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:22052730..22052819;chr1:22052726..22052897 26863196 MeRIP-seq:(Medium) rs889268804 Functional Loss SNV dbSNP153 33..33 33 - - - 63786 RMVar_ID_63786 Human_SNP_ID_5915296 m1A Human chr1 - 22052744 22052744 22052744 AGCTCCCGCGGGGAACCTCGGGCCCCGCACTCACCTCAGCTTCTCCACCGGGGCGTTGGCAGCAC AGCTCCCGCGGGGAACCTCGGGCCCCGCACTCCCCTCAGCTTCTCCACCGGGGCGTTGGCAGCAC T G CDC42-AS1 Ensembl:ENSG00000285752 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:22052718..22053048 26863196 MeRIP-seq:(Medium) rs1454759287 Functional Loss SNV dbSNP153 33..33 33 - - - 63787 RMVar_ID_63787 Human_SNP_ID_5919405 m1A Human chr1 + 22067074 22067074 22067074 GACAGAGCCTGGCACGTCTGGGGAGGTAAGAGACCTGTGTAGCTAGAGCATGGAGAGTACAGGGG GACAGAGCCTGGCACGTCTGGGGAGGTAAGAGGCCTGTGTAGCTAGAGCATGGAGAGTACAGGGG A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:22067064..22067187 26863196 MeRIP-seq:(Medium) rs548618506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10788661 63788 RMVar_ID_63788 Human_SNP_ID_5925715 m1A Human chr1 + 22091618 22091618 22091618 CTAAAGATTAAAAATTAAAATTCGTTTTTGCAATAATGACAAATGCCCTGCACCTACCCACATGC CTAAAGATTAAAAATTAAAATTCGTTTTTGCAGTAATGACAAATGCCCTGCACCTACCCACATGC A G CDC42 Ensembl:ENSG00000070831 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:22091446..22091797 32194978 MeRIP-seq:(Medium) rs533467636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3298161,Human_RBP_ID_5762152 Human_miRNA_ID_267491,Human_miRNA_ID_683721,Human_miRNA_ID_886218,Human_miRNA_ID_1062919,Human_miRNA_ID_1074206,Human_miRNA_ID_2694855 RMVar_hsa_circ_97695,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_95831,RMVar_hsa_circ_105385,RMVar_hsa_circ_130362,RMVar_hsa_circ_130364,RMVar_hsa_circ_130365 63789 RMVar_ID_63789 Human_SNP_ID_5938452 m1A Human chr1 - 22142919 22142919 22142919 GCCCCGGGCCGGGCGCCCGCGGCGGCACCATGAGTCCCCGCTCGTGCCTGCGTTCGCTGCGCCTC GCCCCGGGCCGGGCGCCCGCGGCGGCACCATGGGTCCCCGCTCGTGCCTGCGTTCGCTGCGCCTC T C WNT4 Ensembl:ENSG00000162552 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:22142904..22142989 26863410 MeRIP-seq:(Medium) rs1475315345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_29169 63790 RMVar_ID_63790 Human_SNP_ID_6043045 m1A Human chr1 + 22563636 22563631 22563636 TGGCGCCCCCGCCCGCCCGGCCCGGCCCGGCCATGGCCCCCGCCCGGGGCCGCCTGCCCCCTGCG TGGCGCCCCCGCCCGCCCGGCCCGGCCC_____TGGCCCCCGCCCGGGGCCGCCTGCCCCCTGCG CGGCCA C EPHA8 Ensembl:ENSG00000070886 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:22563543..22563639 26863410 MeRIP-seq:(Medium) rs1557546553 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_4030557 Human_Splice_Rec_29319,Human_Splice_Rec_29351 63791 RMVar_ID_63791 Human_SNP_ID_6043048 m1A Human chr1 + 22563636 22563636 22563636 TGGCGCCCCCGCCCGCCCGGCCCGGCCCGGCCATGGCCCCCGCCCGGGGCCGCCTGCCCCCTGCG TGGCGCCCCCGCCCGCCCGGCCCGGCCCGGCCGTGGCCCCCGCCCGGGGCCGCCTGCCCCCTGCG A G EPHA8 Ensembl:ENSG00000070886 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:22563543..22563639 26863410 MeRIP-seq:(Medium) rs1444999169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4030557 Human_Splice_Rec_29319,Human_Splice_Rec_29351 63792 RMVar_ID_63792 Human_SNP_ID_6120621 m1A Human chr1 + 22864990 22864990 22864990 CCGGAGGCCGAGAGGACCTCGTCTACAACATCATCTGCAAGAGCTGTGGCTCGGGCCGGGGTGCC CCGGAGGCCGAGAGGACCTCGTCTACAACATCGTCTGCAAGAGCTGTGGCTCGGGCCGGGGTGCC A G EPHB2 Ensembl:ENSG00000133216 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:22864942..22865143 32194978 MeRIP-seq:(Medium) rs56180036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2937114 RMVar_hsa_circ_305026,RMVar_hsa_circ_33834,RMVar_hsa_circ_347707,RMVar_hsa_circ_295111,RMVar_hsa_circ_130371,RMVar_hsa_circ_130370 63793 RMVar_ID_63793 Human_SNP_ID_6157378 m1A Human chr1 + 23019610 23019610 23019610 GGCGGCCCGGCGGCCCGAGATGTTATCTGGGAAGAAGGCGGCAGCCGCGGCGGCGGCGGCTGCAG GGCGGCCCGGCGGCCCGAGATGTTATCTGGGAGGAAGGCGGCAGCCGCGGCGGCGGCGGCTGCAG A G KDM1A Ensembl:ENSG00000004487 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:23019509..23019804 26863196 MeRIP-seq:(Medium) rs980731872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_857015,Human_RBP_ID_4073658 RMVar_hsa_circ_130376,RMVar_hsa_circ_84363,RMVar_hsa_circ_122955,RMVar_hsa_circ_130377 63794 RMVar_ID_63794 Human_SNP_ID_6172281 m1A Human chr1 + 23083393 23083393 23083393 GTGAGACAGATGCATTCTAAGGGAAGAGGCCCATGTGCCTGTTTCTGCCATGTAAGGAAGGCTCT GTGAGACAGATGCATTCTAAGGGAAGAGGCCCGTGTGCCTGTTTCTGCCATGTAAGGAAGGCTCT A G KDM1A Ensembl:ENSG00000004487 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23083176..23083490 32194978 MeRIP-seq:(Medium) rs774409559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346382,Human_RBP_ID_2131737,Human_RBP_ID_4091243,Human_RBP_ID_5108483,Human_RBP_ID_17762414,Human_RBP_ID_23205788,Human_RBP_ID_23374332,Human_RBP_ID_26857166 RMVar_hsa_circ_84363,RMVar_hsa_circ_130377,RMVar_hsa_circ_116350,RMVar_hsa_circ_130379,RMVar_hsa_circ_107382,RMVar_hsa_circ_130395,RMVar_hsa_circ_111344,RMVar_hsa_circ_130404,RMVar_hsa_circ_93969,RMVar_hsa_circ_130406,RMVar_hsa_circ_115196,RMVar_hsa_circ_130413,RMVar_hsa_circ_110514,RMVar_hsa_circ_130414,RMVar_hsa_circ_123814,RMVar_hsa_circ_106966,RMVar_hsa_circ_130421,RMVar_hsa_circ_130422,RMVar_hsa_circ_105247,RMVar_hsa_circ_96435,RMVar_hsa_circ_130423,RMVar_hsa_circ_130431,RMVar_hsa_circ_87541,RMVar_hsa_circ_121584,RMVar_hsa_circ_124347,RMVar_hsa_circ_130434,RMVar_hsa_circ_130437,RMVar_hsa_circ_103862,RMVar_hsa_circ_130438,RMVar_hsa_circ_113197,RMVar_hsa_circ_130441,RMVar_hsa_circ_130442 63795 RMVar_ID_63795 Human_SNP_ID_6172282 m1A Human chr1 + 23083393 23083393 23083393 GTGAGACAGATGCATTCTAAGGGAAGAGGCCCATGTGCCTGTTTCTGCCATGTAAGGAAGGCTCT GTGAGACAGATGCATTCTAAGGGAAGAGGCCCTTGTGCCTGTTTCTGCCATGTAAGGAAGGCTCT A T KDM1A Ensembl:ENSG00000004487 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23083176..23083490 32194978 MeRIP-seq:(Medium) rs774409559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346382,Human_RBP_ID_2131737,Human_RBP_ID_4091243,Human_RBP_ID_5108483,Human_RBP_ID_17762414,Human_RBP_ID_23205788,Human_RBP_ID_23374332,Human_RBP_ID_26857166 RMVar_hsa_circ_84363,RMVar_hsa_circ_130377,RMVar_hsa_circ_116350,RMVar_hsa_circ_130379,RMVar_hsa_circ_107382,RMVar_hsa_circ_130395,RMVar_hsa_circ_111344,RMVar_hsa_circ_130404,RMVar_hsa_circ_93969,RMVar_hsa_circ_130406,RMVar_hsa_circ_115196,RMVar_hsa_circ_130413,RMVar_hsa_circ_110514,RMVar_hsa_circ_130414,RMVar_hsa_circ_123814,RMVar_hsa_circ_106966,RMVar_hsa_circ_130421,RMVar_hsa_circ_130422,RMVar_hsa_circ_105247,RMVar_hsa_circ_96435,RMVar_hsa_circ_130423,RMVar_hsa_circ_130431,RMVar_hsa_circ_87541,RMVar_hsa_circ_121584,RMVar_hsa_circ_124347,RMVar_hsa_circ_130434,RMVar_hsa_circ_130437,RMVar_hsa_circ_103862,RMVar_hsa_circ_130438,RMVar_hsa_circ_113197,RMVar_hsa_circ_130441,RMVar_hsa_circ_130442 63796 RMVar_ID_63796 Human_SNP_ID_6173553 m1A Human chr1 - 23087989 23087989 23087989 CTGCCTTCTAGGAAGTGCCCAGCAAGAGGGAAAGCAGACCCCTTTAGTCACTCCACAAGCAATAG CTGCCTTCTAGGAAGTGCCCAGCAAGAGGGAAGGCAGACCCCTTTAGTCACTCCACAAGCAATAG T C AL031428.1,LUZP1 Ensembl:ENSG00000240553,Ensembl:ENSG00000169641 lincRNA,Protein coding exon,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23087867..23088010 32194978 MeRIP-seq:(Medium) rs1375840028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5892018 RMVar_hsa_circ_102152,RMVar_hsa_circ_130443 63797 RMVar_ID_63797 Human_SNP_ID_6178697 m1A Human chr1 - 23109121 23109121 23109121 TTCCATTCTGTTTATATTCTATCCAGGTCAAGAGACAACTGCCTTTGAAAGAGAGTGAGTGACTG TTCCATTCTGTTTATATTCTATCCAGGTCAAGGGACAACTGCCTTTGAAAGAGAGTGAGTGACTG T C LUZP1 Ensembl:ENSG00000169641 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23109081..23109169 26863196 MeRIP-seq:(Medium) rs1055508970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073660,Human_RBP_ID_23374370 Human_Splice_Rec_29700,Human_Splice_Rec_29701,Human_Splice_Rec_29708,Human_Splice_Rec_29709,Human_Splice_Rec_29720,Human_Splice_Rec_29721,Human_Splice_Rec_29726,Human_Splice_Rec_29727 RMVar_hsa_circ_102152,RMVar_hsa_circ_92586,RMVar_hsa_circ_130443,RMVar_hsa_circ_130444,RMVar_hsa_circ_130445,RMVar_hsa_circ_130447,RMVar_hsa_circ_287098,RMVar_hsa_circ_289557,RMVar_hsa_circ_363846,RMVar_hsa_circ_130448 63798 RMVar_ID_63798 Human_SNP_ID_6192898 m1A Human chr1 - 23168152 23168152 23168152 GGCGCGGGGCGCGGGCCGCGGGCCGGGCGGGGAGGGGTCCCGCGGCCGCCGCAGCTGTCGGCCGC GGCGCGGGGCGCGGGCCGCGGGCCGGGCGGGGGGGGGTCCCGCGGCCGCCGCAGCTGTCGGCCGC T C LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23168143..23168333 26863196 MeRIP-seq:(Medium) rs941864413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 63799 RMVar_ID_63799 Human_SNP_ID_6193026 m1A Human chr1 - 23168584 23168584 23168584 AGTTGGGGGAGAGTTGGAATGGATTTTGGAGGAAGGGCTCAGGAGGAGACCTTTTGGGGCGAGAC AGTTGGGGGAGAGTTGGAATGGATTTTGGAGGCAGGGCTCAGGAGGAGACCTTTTGGGGCGAGAC T G LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:23168561..23168648 26863410 MeRIP-seq:(Medium) rs1406038382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328173,Human_RBP_ID_8052514,Human_RBP_ID_8227738,Human_RBP_ID_9410490,Human_RBP_ID_23374684,Human_RBP_ID_24657785 RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 63800 RMVar_ID_63800 Human_SNP_ID_6204765 m1A Human chr1 - 23217002 23217002 23217002 CGCGCGTTGGGGGTGCCCAGCGCCCAGGCGAGAACTGGAGGGGCAGGAAGCACCCCCGGGCCGGG CGCGCGTTGGGGGTGCCCAGCGCCCAGGCGAGTACTGGAGGGGCAGGAAGCACCCCCGGGCCGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23217000..23217120 26863196 MeRIP-seq:(Medium) rs953153324 Functional Loss SNV dbSNP153 33..33 33 - - - 63801 RMVar_ID_63801 Human_SNP_ID_6204890 m1A Human chr1 + 23217388 23217388 23217388 CTCCCCGTCGCGGCCGCCTTGTCTCCGCCGCGACCCCCGCCGAACTCGGGGGCCGCCCGCCCCGC CTCCCCGTCGCGGCCGCCTTGTCTCCGCCGCGCCCCCCGCCGAACTCGGGGGCCGCCCGCCCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23217343..23217515 26863196 MeRIP-seq:(Medium) rs879778407 Functional Loss SNV dbSNP153 33..33 33 - - - 63802 RMVar_ID_63802 Human_SNP_ID_6227465 m1A Human chr1 + 23310472 23310472 23310472 AAGCCCTTACTTGTCTACTTCCACTGTTGCCCATAAGTATCCTGATAAAATTCCTGGTTGTCATT AAGCCCTTACTTGTCTACTTCCACTGTTGCCCGTAAGTATCCTGATAAAATTCCTGGTTGTCATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23310426..23310600 32194978 MeRIP-seq:(Medium) rs757788976 Functional Loss SNV dbSNP153 33..33 33 - - - 63803 RMVar_ID_63803 Human_SNP_ID_6227514 m1A Human chr1 - 23310676 23310676 23310676 GCTCAACAGCAGAGAGGCCGTGGTTCCCGTGGATCTCGGGGCAATCGTGGGGGCAATGTAGGAGG GCTCAACAGCAGAGAGGCCGTGGTTCCCGTGGTTCTCGGGGCAATCGTGGGGGCAATGTAGGAGG T A HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23310626..23310800 32194978 MeRIP-seq:(Medium) rs1332197225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347383,Human_RBP_ID_976385,Human_RBP_ID_3304155,Human_RBP_ID_4035307,Human_RBP_ID_5786291,Human_RBP_ID_8746002,Human_RBP_ID_10858269,Human_RBP_ID_26309667,Human_RBP_ID_27153166,Human_RBP_ID_27395745 63804 RMVar_ID_63804 Human_SNP_ID_6227528 m1A Human chr1 + 23310712 23310712 23310712 CGGGAACCACGGCCTCTCTGCTGTTGAGCAGGACCCCCTCTGCCACCCCTAGAGCCTCTTGGTGG CGGGAACCACGGCCTCTCTGCTGTTGAGCAGGGCCCCCTCTGCCACCCCTAGAGCCTCTTGGTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:23310661..23310989 26863196 MeRIP-seq:(Medium) rs367940950 Functional Loss SNV dbSNP153 33..33 33 - - - 63805 RMVar_ID_63805 Human_SNP_ID_6227652 m1A Human chr1 - 23311061 23311061 23311061 TCTTTTCTCCCTTCTCTACTTTGCTAGGTATGAAGATTATTACTACCACCCTCCTCCTCGCATGC TCTTTTCTCCCTTCTCTACTTTGCTAGGTATGGAGATTATTACTACCACCCTCCTCCTCGCATGC T C HNRNPR Ensembl:ENSG00000125944 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1242108957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1153182,Human_RBP_ID_1425238,Human_RBP_ID_2134652,Human_RBP_ID_9355671,Human_RBP_ID_17744366,Human_RBP_ID_21962853,Human_RBP_ID_24761101,Human_RBP_ID_26310472,Human_RBP_ID_27797529 Human_Splice_Rec_29742,Human_Splice_Rec_29766,Human_Splice_Rec_29782,Human_Splice_Rec_29800,Human_Splice_Rec_29804,Human_Splice_Rec_29824,Human_Splice_Rec_29840,Human_Splice_Rec_29856 63806 RMVar_ID_63806 Human_SNP_ID_6234879 m1A Human chr1 - 23337798 23337798 23337798 AGACCTACAGGCAGAGAGAGAAACAGGGGAGCAAGGTGCAAGAGTCCACAAAGGGACCTGATGAA AGACCTACAGGCAGAGAGAGAAACAGGGGAGCTAGGTGCAAGAGTCCACAAAGGGACCTGATGAA T A HNRNPR Ensembl:ENSG00000125944 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23337751..23337825 32194978 MeRIP-seq:(Medium) rs971307585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221687,Human_RBP_ID_742412,Human_RBP_ID_802405,Human_RBP_ID_857489,Human_RBP_ID_1425359,Human_RBP_ID_1741593,Human_RBP_ID_2134778,Human_RBP_ID_4035471,Human_RBP_ID_5787139,Human_RBP_ID_9355690,Human_RBP_ID_18967579,Human_RBP_ID_19034231,Human_RBP_ID_22858374,Human_RBP_ID_23376449,Human_RBP_ID_26310483,Human_RBP_ID_27797543 Human_Splice_Rec_29752,Human_Splice_Rec_29753,Human_Splice_Rec_29770,Human_Splice_Rec_29771,Human_Splice_Rec_29788,Human_Splice_Rec_29789,Human_Splice_Rec_29810,Human_Splice_Rec_29811,Human_Splice_Rec_29828,Human_Splice_Rec_29829,Human_Splice_Rec_29844,Human_Splice_Rec_29845,Human_Splice_Rec_29858,Human_Splice_Rec_29859,Human_Splice_Rec_29874,Human_Splice_Rec_29875 Human_miRNA_ID_2401769,Human_miRNA_ID_2749864 RMVar_hsa_circ_67146,RMVar_hsa_circ_305724,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_51552,RMVar_hsa_circ_130450,RMVar_hsa_circ_280163,RMVar_hsa_circ_331690,RMVar_hsa_circ_54577,RMVar_hsa_circ_361638,RMVar_hsa_circ_130452,RMVar_hsa_circ_349427 63807 RMVar_ID_63807 Human_SNP_ID_6235623 m1A Human chr1 - 23341008 23341008 23341008 AGCTCCTGAATTTTTTCCAGCAGCATAATAAAATGGCTAATCAGGTGAATGGTAATGCGGTACAG AGCTCCTGAATTTTTTCCAGCAGCATAATAAAGTGGCTAATCAGGTGAATGGTAATGCGGTACAG T C HNRNPR Ensembl:ENSG00000125944 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:23340960..23341053 26863196 MeRIP-seq:(Medium) rs1448233539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19335,Human_RBP_ID_1741617,Human_RBP_ID_2134790,Human_RBP_ID_4076647,Human_RBP_ID_10860054,Human_RBP_ID_17334375 Human_Splice_Rec_29748,Human_Splice_Rec_29784,Human_Splice_Rec_29806,Human_Splice_Rec_29884 RMVar_hsa_circ_320103,RMVar_hsa_circ_280163,RMVar_hsa_circ_331690,RMVar_hsa_circ_2795,RMVar_hsa_circ_31051,RMVar_hsa_circ_361638,RMVar_hsa_circ_130452,RMVar_hsa_circ_336058,RMVar_hsa_circ_130453 63808 RMVar_ID_63808 Human_SNP_ID_6249412 m1A Human chr1 + 23392605 23392605 23392605 CACTCCACACATCATACACACACACTCCACACATCATACACACACACACACACTCCACACATCAT CACTCCACACATCATACACACACACTCCACACGTCATACACACACACACACACTCCACACATCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:23392539..23392650 26863196 MeRIP-seq:(Medium) rs62642604 Functional Loss SNV dbSNP153 33..33 33 - - - 63809 RMVar_ID_63809 Human_SNP_ID_6257287 m1A Human chr1 - 23424609 23424609 23424609 GGGCCAACATGGGCCAGGAAGAGGAGCTGCTGAGGATCGCCAAAAAGCTGGAGAAGATGGTGGCC GGGCCAACATGGGCCAGGAAGAGGAGCTGCTGCGGATCGCCAAAAAGCTGGAGAAGATGGTGGCC T G TCEA3 Ensembl:ENSG00000204219 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:23424505..23424727 26863196 MeRIP-seq:(Medium) rs758901775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9355710 Human_Splice_Rec_29913,Human_Splice_Rec_29931,Human_Splice_Rec_29949 63810 RMVar_ID_63810 Human_SNP_ID_6271838 m1A Human chr1 - 23484045 23484045 23484045 CTCCCCGGCTGGGGCCGCCGCCTTCGCCGCCAAGATGCCCCGGTACCGAGGGGCGGCGCTGGCGC CTCCCCGGCTGGGGCCGCCGCCTTCGCCGCCACGATGCCCCGGTACCGAGGGGCGGCGCTGGCGC T G ASAP3 Ensembl:ENSG00000088280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23484016..23484199 26863196 MeRIP-seq:(Medium) rs1032534820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073667,Human_RBP_ID_18568234,Human_RBP_ID_18967601 Human_Splice_Rec_29993,Human_Splice_Rec_30043,Human_Splice_Rec_30065,Human_Splice_Rec_30113,Human_Splice_Rec_30193,Human_Splice_Rec_30211 RMVar_hsa_circ_87437,RMVar_hsa_circ_106292,RMVar_hsa_circ_130467,RMVar_hsa_circ_130468,RMVar_hsa_circ_110021,RMVar_hsa_circ_130470,RMVar_hsa_circ_91857,RMVar_hsa_circ_130469,RMVar_hsa_circ_127245,RMVar_hsa_circ_130471 63811 RMVar_ID_63811 Human_SNP_ID_6271839 m1A Human chr1 + 23484055 23484046 23484055 CGCCCCTCGGTACCGGGGCATCTTGGCGGCGAAGGCGGCGGCCCCAGCCGGGGAGCTGAGGTCCT CGCCCCTCGGTACCGGGGCATCTT_________GGCGGCGGCCCCAGCCGGGGAGCTGAGGTCCT TGGCGGCGAA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23483955..23484404 26863196 MeRIP-seq:(Medium) rs748336664 Functional Loss DEL dbSNP153 25..33 33 - - - 63812 RMVar_ID_63812 Human_SNP_ID_6279084 m1A Human chr1 + 23510025 23510025 23510025 TCAGAGGGGAGCTGCACGCCAGGGTCGGGGACAGGAACTGGTCCTCAGTCTGCTGCAGGAGTGGG TCAGAGGGGAGCTGCACGCCAGGGTCGGGGACGGGAACTGGTCCTCAGTCTGCTGCAGGAGTGGG A G lnc-RPL11-6,lnc-BBS5-6 RNACentral:URS00008B73E3,RNACentral:URS0000E2127A lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:23509976..23510137 26863196 MeRIP-seq:(Medium) rs1016525076 Functional Loss SNV dbSNP153 33..33 33 - - - 63813 RMVar_ID_63813 Human_SNP_ID_6280691 m1A Human chr1 + 23516390 23516389 23516391 ATGCTAGGGTCGGTGCTGCTGCTGGGCTGGGCAGAGTCAGGGCTGGGGCAGAGGGTGGAGGTAGA ATGCTAGGGTCGGTGCTGCTGCTGGGCTGGGC__AGTCAGGGCTGGGGCAGAGGGTGGAGGTAGA CAG C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23516297..23516461 26863196 MeRIP-seq:(Medium) rs1468745393 Functional Loss DEL dbSNP153 33..34 33 - - - 63814 RMVar_ID_63814 Human_SNP_ID_6280692 m1A Human chr1 + 23516390 23516390 23516390 ATGCTAGGGTCGGTGCTGCTGCTGGGCTGGGCAGAGTCAGGGCTGGGGCAGAGGGTGGAGGTAGA ATGCTAGGGTCGGTGCTGCTGCTGGGCTGGGCGGAGTCAGGGCTGGGGCAGAGGGTGGAGGTAGA A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23516297..23516461 26863196 MeRIP-seq:(Medium) rs765245474 Functional Loss SNV dbSNP153 33..33 33 - - - 63815 RMVar_ID_63815 Human_SNP_ID_6284589 m1A Human chr1 - 23531199 23531199 23531199 AGAAAGACTCAAGGACTAGAGAGCGAGCCGCAAGGAAGTCGGTGCAGTCGAGACCCCCCTCCCCA AGAAAGACTCAAGGACTAGAGAGCGAGCCGCAGGGAAGTCGGTGCAGTCGAGACCCCCCTCCCCA T C E2F2 Ensembl:ENSG00000007968 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:23530929..23531275;chr1:23530975..23531263 26863196 MeRIP-seq:(Medium) rs1293794384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1425658,Human_RBP_ID_4073669 63816 RMVar_ID_63816 Human_SNP_ID_6290739 m1A Human chr1 + 23554168 23554168 23554168 AGAGAACTCCTCCCTCCTTAATCTGGTTTGTCAAAGGCAACCCCCAAAGTCCCGGTCTCAAGGTG AGAGAACTCCTCCCTCCTTAATCTGGTTTGTCCAAGGCAACCCCCAAAGTCCCGGTCTCAAGGTG A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:23554127..23554311 26863196 MeRIP-seq:(Medium) rs932138497 Functional Loss SNV dbSNP153 33..33 33 - - - 63817 RMVar_ID_63817 Human_SNP_ID_6292330 m1A Human chr1 - 23558360 23558360 23558360 TGCCTGGGACCCCGGGAACCTCTCCTGCCGGAAGCCGGACGGCAGGGATGGGCCCCAACTTCGCC TGCCTGGGACCCCGGGAACCTCTCCTGCCGGACGCCGGACGGCAGGGATGGGCCCCAACTTCGCC T G ID3 Ensembl:ENSG00000117318 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23558126..23558446 32194978 MeRIP-seq:(Medium) rs1306181872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220879,Human_RBP_ID_347766,Human_RBP_ID_17647401,Human_RBP_ID_18186967,Human_RBP_ID_27395946 Human_Splice_Rec_30240,Human_Splice_Rec_30242 RMVar_hsa_circ_130476,RMVar_hsa_circ_100881,RMVar_hsa_circ_124280,RMVar_hsa_circ_130477 63818 RMVar_ID_63818 Human_SNP_ID_6292638 m1A Human chr1 + 23558989 23558989 23558989 GAGTCAGTGGCAAAAGCTCCTTTTGTCGTTGGAGATGACAAGTTCCGGAGTGAGCTCGGCTGTCT GAGTCAGTGGCAAAAGCTCCTTTTGTCGTTGGCGATGACAAGTTCCGGAGTGAGCTCGGCTGTCT A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23558926..23559025 32194978 MeRIP-seq:(Medium) rs11542317 Functional Loss SNV dbSNP153 33..33 33 - - - 63819 RMVar_ID_63819 Human_SNP_ID_6292660 m1A Human chr1 - 23559012 23559012 23559012 CTCTTCCCTCTTTTCCTCTAATCAGACAGCCGAGCTCACTCCGGAACTTGTCATCTCCAACGACA CTCTTCCCTCTTTTCCTCTAATCAGACAGCCGTGCTCACTCCGGAACTTGTCATCTCCAACGACA T A ID3 Ensembl:ENSG00000117318 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23558909..23559025 26863196 MeRIP-seq:(Medium) rs779331497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858625,Human_RBP_ID_2135144,Human_RBP_ID_4036507,Human_RBP_ID_5331262,Human_RBP_ID_9318697,Human_RBP_ID_19034254,Human_RBP_ID_22426990,Human_RBP_ID_22633149,Human_RBP_ID_22748965,Human_RBP_ID_24664723 Human_Splice_Rec_30238,Human_Splice_Rec_30239,Human_Splice_Rec_30241,Human_Splice_Rec_30244 RMVar_hsa_circ_124280,RMVar_hsa_circ_130477,RMVar_hsa_circ_121237,RMVar_hsa_circ_130478 63820 RMVar_ID_63820 Human_SNP_ID_6292661 m1A Human chr1 - 23559012 23559012 23559012 CTCTTCCCTCTTTTCCTCTAATCAGACAGCCGAGCTCACTCCGGAACTTGTCATCTCCAACGACA CTCTTCCCTCTTTTCCTCTAATCAGACAGCCGGGCTCACTCCGGAACTTGTCATCTCCAACGACA T C ID3 Ensembl:ENSG00000117318 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23558909..23559025 26863196 MeRIP-seq:(Medium) rs779331497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858625,Human_RBP_ID_2135144,Human_RBP_ID_4036507,Human_RBP_ID_5331262,Human_RBP_ID_9318697,Human_RBP_ID_19034254,Human_RBP_ID_22426990,Human_RBP_ID_22633149,Human_RBP_ID_22748965,Human_RBP_ID_24664723 Human_Splice_Rec_30238,Human_Splice_Rec_30239,Human_Splice_Rec_30241,Human_Splice_Rec_30244 RMVar_hsa_circ_124280,RMVar_hsa_circ_130477,RMVar_hsa_circ_121237,RMVar_hsa_circ_130478 63821 RMVar_ID_63821 Human_SNP_ID_6292763 m1A Human chr1 + 23559160 23559160 23559160 TGGATGGGAAGGTGGGGGCCATCAGGGGGTCCAGGGGCTGGCTCGGCCAGGACTACCTGCAGGTC TGGATGGGAAGGTGGGGGCCATCAGGGGGTCCGGGGGCTGGCTCGGCCAGGACTACCTGCAGGTC A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:23558895..23559413 26863196 MeRIP-seq:(Medium) rs201313484 Functional Loss SNV dbSNP153 33..33 33 - - - 63822 RMVar_ID_63822 Human_SNP_ID_6292868 m1A Human chr1 - 23559343 23559343 23559343 TCGGAACGCAGTCTGGCCATCGCCCGGGGCCGAGGGAAGGGCCCGGCAGCTGAGGAGCCGCTGAG TCGGAACGCAGTCTGGCCATCGCCCGGGGCCGCGGGAAGGGCCCGGCAGCTGAGGAGCCGCTGAG T G ID3 Ensembl:ENSG00000117318 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:23558944..23559500;chr1:23559126..23559475 32194978 MeRIP-seq:(Medium) rs761142520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1154,Human_RBP_ID_347768,Human_RBP_ID_1254178,Human_RBP_ID_4073670,Human_RBP_ID_18967605,Human_RBP_ID_22428210,Human_RBP_ID_22750862,Human_RBP_ID_22871728,Human_RBP_ID_27178965 Human_miRNA_ID_2239960 RMVar_hsa_circ_124280,RMVar_hsa_circ_130477 63823 RMVar_ID_63823 Human_SNP_ID_6292931 m1A Human chr1 + 23559445 23559445 23559445 CTCAGCGCCTTCATGCTGGGGAGTGAGTCCAGAGGTGCCCCAAAGAGAAAGAAAACCAAAAGAAG CTCAGCGCCTTCATGCTGGGGAGTGAGTCCAGCGGTGCCCCAAAGAGAAAGAAAACCAAAAGAAG A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:23559073..23559525;chr1:23559191..23559500;chr1:23559176..23559525 26863196 MeRIP-seq:(Medium) rs966157360 Functional Loss SNV dbSNP153 33..33 33 - - - 63824 RMVar_ID_63824 Human_SNP_ID_6292932 m1A Human chr1 + 23559445 23559445 23559445 CTCAGCGCCTTCATGCTGGGGAGTGAGTCCAGAGGTGCCCCAAAGAGAAAGAAAACCAAAAGAAG CTCAGCGCCTTCATGCTGGGGAGTGAGTCCAGGGGTGCCCCAAAGAGAAAGAAAACCAAAAGAAG A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:23559073..23559525;chr1:23559191..23559500;chr1:23559176..23559525 26863196 MeRIP-seq:(Medium) rs966157360 Functional Loss SNV dbSNP153 33..33 33 - - - 63825 RMVar_ID_63825 Human_SNP_ID_6327170 m1A Human chr1 - 23692677 23692677 23692677 GCTCGCGTCAGTCTGTCTCCACTCTCCCCAACACAGATGTTGAGACAGAGTTTGCGGATGCGAAG GCTCGCGTCAGTCTGTCTCCACTCTCCCCAACGCAGATGTTGAGACAGAGTTTGCGGATGCGAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23692627..23692810 26863196 MeRIP-seq:(Medium) rs1804294 Functional Loss SNV dbSNP153 33..33 33 - - - 63826 RMVar_ID_63826 Human_SNP_ID_6327536 m1A Human chr1 + 23693874 23693874 23693874 AATGAAAAGATTGCTGTCCACTGCACAGTTCGAGGGGCCAAGGCAGAAGAAATCTTGGAGAAGGG AATGAAAAGATTGCTGTCCACTGCACAGTTCGTGGGGCCAAGGCAGAAGAAATCTTGGAGAAGGG A T RPL11 Ensembl:ENSG00000142676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23693751..23693963 26863196 MeRIP-seq:(Medium) rs1348324736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20642,Human_RBP_ID_347784,Human_RBP_ID_742983,Human_RBP_ID_802167,Human_RBP_ID_856840,Human_RBP_ID_976499,Human_RBP_ID_1439366,Human_RBP_ID_1742039,Human_RBP_ID_3304898,Human_RBP_ID_4036549,Human_RBP_ID_5789448,Human_RBP_ID_8304184,Human_RBP_ID_8746370,Human_RBP_ID_8966199,Human_RBP_ID_10865050,Human_RBP_ID_17216953,Human_RBP_ID_17456198,Human_RBP_ID_17677174,Human_RBP_ID_17763459,Human_RBP_ID_18429894,Human_RBP_ID_18568277,Human_RBP_ID_22019484,Human_RBP_ID_22487501,Human_RBP_ID_23377243,Human_RBP_ID_26800055 Human_Splice_Rec_30290,Human_Splice_Rec_30291,Human_Splice_Rec_30300,Human_Splice_Rec_30301,Human_Splice_Rec_30308,Human_Splice_Rec_30309,Human_Splice_Rec_30318,Human_Splice_Rec_30319,Human_Splice_Rec_30326,Human_Splice_Rec_30327,Human_Splice_Rec_30334,Human_Splice_Rec_30335 Human_miRNA_ID_2216578,Human_miRNA_ID_2216579 RMVar_hsa_circ_89818,RMVar_hsa_circ_122043,RMVar_hsa_circ_106898,RMVar_hsa_circ_130481,RMVar_hsa_circ_130482,RMVar_hsa_circ_368746,RMVar_hsa_circ_113682,RMVar_hsa_circ_130484,RMVar_hsa_circ_67667,RMVar_hsa_circ_130485,RMVar_hsa_circ_378859,RMVar_hsa_circ_374321,RMVar_hsa_circ_130487,RMVar_hsa_circ_111565,RMVar_hsa_circ_130488,RMVar_hsa_circ_130486 63827 RMVar_ID_63827 Human_SNP_ID_6327549 m1A Human chr1 + 23693900 23693900 23693900 AGTTCGAGGGGCCAAGGCAGAAGAAATCTTGGAGAAGGGTCTAAAGGTGAGCCTAATCCCCTAAT AGTTCGAGGGGCCAAGGCAGAAGAAATCTTGGGGAAGGGTCTAAAGGTGAGCCTAATCCCCTAAT A G RPL11 Ensembl:ENSG00000142676 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:23693849..23693951 26863196 MeRIP-seq:(Medium) rs771576117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222073,Human_RBP_ID_347785,Human_RBP_ID_742983,Human_RBP_ID_802167,Human_RBP_ID_856840,Human_RBP_ID_976499,Human_RBP_ID_1742039,Human_RBP_ID_4036549,Human_RBP_ID_5109474,Human_RBP_ID_5789448,Human_RBP_ID_8966199,Human_RBP_ID_10865052,Human_RBP_ID_17456198,Human_RBP_ID_17744907,Human_RBP_ID_18429895,Human_RBP_ID_23122357,Human_RBP_ID_23377243,Human_RBP_ID_26800056,Human_RBP_ID_27590896 Human_Splice_Rec_30290,Human_Splice_Rec_30291,Human_Splice_Rec_30300,Human_Splice_Rec_30301,Human_Splice_Rec_30308,Human_Splice_Rec_30309,Human_Splice_Rec_30318,Human_Splice_Rec_30319,Human_Splice_Rec_30326,Human_Splice_Rec_30327,Human_Splice_Rec_30334,Human_Splice_Rec_30335 Human_miRNA_ID_2787565,Human_miRNA_ID_2787566,Human_miRNA_ID_2817178,Human_miRNA_ID_2817179 RMVar_hsa_circ_89818,RMVar_hsa_circ_122043,RMVar_hsa_circ_106898,RMVar_hsa_circ_130481,RMVar_hsa_circ_130482,RMVar_hsa_circ_368746,RMVar_hsa_circ_113682,RMVar_hsa_circ_130484,RMVar_hsa_circ_67667,RMVar_hsa_circ_130485,RMVar_hsa_circ_378859,RMVar_hsa_circ_374321,RMVar_hsa_circ_130487,RMVar_hsa_circ_111565,RMVar_hsa_circ_130488,RMVar_hsa_circ_130486 63828 RMVar_ID_63828 Human_SNP_ID_6328106 m1A Human chr1 + 23695845 23695845 23695845 GGTTTCAGCATCGCAGACAAGAAGCGCAGGACAGGCTGCATTGGGGCCAAACACAGAATCAGCAA GGTTTCAGCATCGCAGACAAGAAGCGCAGGACGGGCTGCATTGGGGCCAAACACAGAATCAGCAA A G RPL11 Ensembl:ENSG00000142676 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:23695776..23695925;chr1:23695776..23695962 32194978 MeRIP-seq:(Medium) rs1032506542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20645,Human_RBP_ID_222077,Human_RBP_ID_347798,Human_RBP_ID_802170,Human_RBP_ID_856842,Human_RBP_ID_1122990,Human_RBP_ID_1153306,Human_RBP_ID_1425706,Human_RBP_ID_1742048,Human_RBP_ID_4092074,Human_RBP_ID_5155996,Human_RBP_ID_5789474,Human_RBP_ID_8304198,Human_RBP_ID_8966205,Human_RBP_ID_10865123,Human_RBP_ID_17216957,Human_RBP_ID_17451328,Human_RBP_ID_17647409,Human_RBP_ID_18568287,Human_RBP_ID_19313473,Human_RBP_ID_22429148,Human_RBP_ID_23122361,Human_RBP_ID_23147825,Human_RBP_ID_27178980,Human_RBP_ID_27590916 Human_Splice_Rec_30294,Human_Splice_Rec_30295,Human_Splice_Rec_30303,Human_Splice_Rec_30312,Human_Splice_Rec_30313,Human_Splice_Rec_30322,Human_Splice_Rec_30323,Human_Splice_Rec_30330,Human_Splice_Rec_30331,Human_Splice_Rec_30338 Human_miRNA_ID_2224707 RMVar_hsa_circ_77082,RMVar_hsa_circ_89818,RMVar_hsa_circ_106898,RMVar_hsa_circ_130482,RMVar_hsa_circ_130484,RMVar_hsa_circ_67667,RMVar_hsa_circ_111565,RMVar_hsa_circ_130488,RMVar_hsa_circ_375194,RMVar_hsa_circ_130492,RMVar_hsa_circ_81192,RMVar_hsa_circ_130490,RMVar_hsa_circ_130491,RMVar_hsa_circ_318231,RMVar_hsa_circ_130493 63829 RMVar_ID_63829 Human_SNP_ID_6340542 m1A Human chr1 - 23743523 23743523 23743523 CCAGGCGCGCCTGCAGCTTCTCCACAACTTGGAGCGCCGACTCCGCCGCCATCGCTGTCACTGGC CCAGGCGCGCCTGCAGCTTCTCCACAACTTGGGGCGCCGACTCCGCCGCCATCGCTGTCACTGGC T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23743379..23743647 26863196 MeRIP-seq:(Medium) rs1363250948 Functional Loss SNV dbSNP153 33..33 33 - - - 63830 RMVar_ID_63830 Human_SNP_ID_6342491 m1A Human chr1 + 23750956 23750956 23750956 GAGATGGAGGGGGACTACCAAGAAACCTGGAAAGCCACGGGGAGCCGATCCTATAGCCCTGACCA GAGATGGAGGGGGACTACCAAGAAACCTGGAAGGCCACGGGGAGCCGATCCTATAGCCCTGACCA A G ELOA Ensembl:ENSG00000011007 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23750907..23751068 26863196 MeRIP-seq:(Medium) rs1312416276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16804,Human_RBP_ID_859080,Human_RBP_ID_1425902,Human_RBP_ID_1742172,Human_RBP_ID_3933062,Human_RBP_ID_5109863,Human_RBP_ID_5642193,Human_RBP_ID_9355715,Human_RBP_ID_18409912,Human_RBP_ID_18568428,Human_RBP_ID_22558168,Human_RBP_ID_26310490,Human_RBP_ID_27797546 RMVar_hsa_circ_63285,RMVar_hsa_circ_68345,RMVar_hsa_circ_292762,RMVar_hsa_circ_313685,RMVar_hsa_circ_118244,RMVar_hsa_circ_130496,RMVar_hsa_circ_44005,RMVar_hsa_circ_271337,RMVar_hsa_circ_58058 63831 RMVar_ID_63831 Human_SNP_ID_6345328 m1A Human chr1 + 23760930 23760930 23760930 AACCCACTTGGTTGTGACCCAGGTAGAGGTAGATGCCATACATTTGAGATATGCGTCCTTAAGGA AACCCACTTGGTTGTGACCCAGGTAGAGGTAGGTGCCATACATTTGAGATATGCGTCCTTAAGGA A G ELOA Ensembl:ENSG00000011007 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23760880..23761130 32194978 MeRIP-seq:(Medium) rs1308580317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347894,Human_RBP_ID_10867400,Human_RBP_ID_17745121,Human_RBP_ID_22558170,Human_RBP_ID_23377630,Human_RBP_ID_26377466 63832 RMVar_ID_63832 Human_SNP_ID_6350032 m1A Human chr1 + 23778457 23778457 23778457 GGAGCTGAACGGCGCGGAGCTGGTCTGAGGCGAGCCGAGCCGAGCGAGCGCGGCGGTGGGGCCGA GGAGCTGAACGGCGCGGAGCTGGTCTGAGGCGTGCCGAGCCGAGCGAGCGCGGCGGTGGGGCCGA A T PITHD1 Ensembl:ENSG00000057757 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:23778401..23778647;chr1:23778401..23778700 26863196 MeRIP-seq:(Medium) rs1238807761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221063,Human_RBP_ID_347927,Human_RBP_ID_4073678,Human_RBP_ID_5311583,Human_RBP_ID_9318701,Human_RBP_ID_10867734,Human_RBP_ID_17668299,Human_RBP_ID_18414892,Human_RBP_ID_22426999,Human_RBP_ID_22870771,Human_RBP_ID_23377678 RMVar_hsa_circ_88041,RMVar_hsa_circ_130497 63833 RMVar_ID_63833 Human_SNP_ID_6350043 m1A Human chr1 + 23778467 23778467 23778467 GGCGCGGAGCTGGTCTGAGGCGAGCCGAGCCGAGCGAGCGCGGCGGTGGGGCCGAGAGGACGCGC GGCGCGGAGCTGGTCTGAGGCGAGCCGAGCCGGGCGAGCGCGGCGGTGGGGCCGAGAGGACGCGC A G PITHD1 Ensembl:ENSG00000057757 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:23778423..23778575 26863196 MeRIP-seq:(Medium) rs1469318543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221063,Human_RBP_ID_347927,Human_RBP_ID_4073678,Human_RBP_ID_5311583,Human_RBP_ID_9318701,Human_RBP_ID_17668299,Human_RBP_ID_18414892,Human_RBP_ID_22426999,Human_RBP_ID_22870771 RMVar_hsa_circ_88041,RMVar_hsa_circ_130497 63834 RMVar_ID_63834 Human_SNP_ID_6350046 m1A Human chr1 + 23778491 23778469 23778491 CCGAGCCGAGCGAGCGCGGCGGTGGGGCCGAGAGGACGCGCAGGTGGCGGCGTTGCCATGTCGCA CCGAGCCGAGC______________________GGACGCGCAGGTGGCGGCGTTGCCATGTCGCA CGAGCGCGGCGGTGGGGCCGAGA C PITHD1 Ensembl:ENSG00000057757 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:23778444..23778647 26863196 MeRIP-seq:(Medium) rs1361049347 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_4036908,Human_RBP_ID_5312379,Human_RBP_ID_17668299,Human_RBP_ID_18414892,Human_RBP_ID_22426999,Human_RBP_ID_22870771 Human_miRNA_ID_2569819,Human_miRNA_ID_3043586 RMVar_hsa_circ_88041,RMVar_hsa_circ_130497 63835 RMVar_ID_63835 Human_SNP_ID_6350080 m1A Human chr1 - 23778545 23778545 23778545 GGCTCCTCCCGTTCGGCGGCGCAGCGGCAGCCACCCCCGCCGTGGCTGTGACCGTGCGACATGGC GGCTCCTCCCGTTCGGCGGCGCAGCGGCAGCCCCCCCCGCCGTGGCTGTGACCGTGCGACATGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:23778444..23778625 26863410 MeRIP-seq:(Medium) rs373570147 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 63836 RMVar_ID_63836 Human_SNP_ID_6352704 m1A Human chr1 + 23787752 23787752 23787752 TTTTTTTGTTTTTGTTTTTGTTTTTTTAAAGGAAACTATTTGTGGGCTATAGGAAACTTTCTGAT TTTTTTTGTTTTTGTTTTTGTTTTTTTAAAGGCAACTATTTGTGGGCTATAGGAAACTTTCTGAT A C PITHD1 Ensembl:ENSG00000057757 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23787701..23787775 32194978 MeRIP-seq:(Medium) rs1355469547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347945,Human_RBP_ID_976563,Human_RBP_ID_1075114,Human_RBP_ID_1742212,Human_RBP_ID_2135405,Human_RBP_ID_3305399,Human_RBP_ID_5790878,Human_RBP_ID_10867908,Human_RBP_ID_23205020,Human_RBP_ID_23377713,Human_RBP_ID_24451413,Human_RBP_ID_26377491 RMVar_hsa_circ_106493,RMVar_hsa_circ_88041,RMVar_hsa_circ_130497,RMVar_hsa_circ_76190,RMVar_hsa_circ_130498,RMVar_hsa_circ_130499 63837 RMVar_ID_63837 Human_SNP_ID_6353666 m1A Human chr1 + 23791221 23791221 23791221 GTGTGTCTGCGGGAGAAAGAGGAGAATCGCCCAAGCGGCCTCGGAAGTCCCAGGGAGTGGAGGTA GTGTGTCTGCGGGAGAAAGAGGAGAATCGCCCGAGCGGCCTCGGAAGTCCCAGGGAGTGGAGGTA A G LYPLA2 Ensembl:ENSG00000011009 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:23791151..23791989;chr1:23791151..23791311 26863196 MeRIP-seq:(Medium) rs571664320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223483,Human_RBP_ID_801440,Human_RBP_ID_4073679,Human_RBP_ID_22871203,Human_RBP_ID_23205023,Human_RBP_ID_24359550,Human_RBP_ID_26310500 Human_Splice_Rec_30449,Human_Splice_Rec_30467,Human_Splice_Rec_30481,Human_Splice_Rec_30493,Human_Splice_Rec_30509,Human_Splice_Rec_30527 63838 RMVar_ID_63838 Human_SNP_ID_6355136 m1A Human chr1 - 23795881 23795879 23795881 GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTCAGGGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTC__GGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC CCT C GALE Ensembl:ENSG00000117308 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23795697..23796046 32194978 MeRIP-seq:(Medium) rs977929691 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_347980,Human_RBP_ID_17745187,Human_RBP_ID_27396016 Human_miRNA_ID_118524,Human_miRNA_ID_122332 63839 RMVar_ID_63839 Human_SNP_ID_6355138 m1A Human chr1 - 23795881 23795881 23795881 GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTCAGGGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTCGGGGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC T C GALE Ensembl:ENSG00000117308 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23795697..23796046 32194978 MeRIP-seq:(Medium) rs1482922413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347980,Human_RBP_ID_17745187,Human_RBP_ID_27396016 Human_miRNA_ID_118524,Human_miRNA_ID_122332 63840 RMVar_ID_63840 Human_SNP_ID_6355139 m1A Human chr1 - 23795881 23795881 23795881 GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTCAGGGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC GCTGCCTGCTCTCCAGCCTCTGGCAGGAACTCCGGGCCCTGGAGCTGCTGGGGCCAAGCCAAGGC T G GALE Ensembl:ENSG00000117308 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23795697..23796046 32194978 MeRIP-seq:(Medium) rs1482922413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347980,Human_RBP_ID_17745187,Human_RBP_ID_27396016 Human_miRNA_ID_118524,Human_miRNA_ID_122332 63841 RMVar_ID_63841 Human_SNP_ID_6355947 m1A Human chr1 - 23797775 23797775 23797775 CCCAGTACCTGCCCCTTGATGAGGCCCACCCCACGGGTGGTTGTACCAACCCTTACGGCAAGTCC CCCAGTACCTGCCCCTTGATGAGGCCCACCCCGCGGGTGGTTGTACCAACCCTTACGGCAAGTCC T C GALE Ensembl:ENSG00000117308 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:23797726..23797775 32194978 MeRIP-seq:(Medium) rs746065738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26797915 Human_Splice_Rec_30588,Human_Splice_Rec_30589,Human_Splice_Rec_30604,Human_Splice_Rec_30605,Human_Splice_Rec_30624,Human_Splice_Rec_30625,Human_Splice_Rec_30650,Human_Splice_Rec_30651,Human_Splice_Rec_30668,Human_Splice_Rec_30669,Human_Splice_Rec_30682,Human_Splice_Rec_30683,Human_Splice_Rec_30694,Human_Splice_Rec_30695,Human_Splice_Rec_30704,Human_Splice_Rec_30705,Human_Splice_Rec_30712,Human_Splice_Rec_30713,Human_Splice_Rec_30718 RMVar_hsa_circ_40010,RMVar_hsa_circ_130506,RMVar_hsa_circ_360291,RMVar_hsa_circ_370342,RMVar_hsa_circ_59202 63842 RMVar_ID_63842 Human_SNP_ID_6356828 m1A Human chr1 - 23800644 23800642 23800644 CGAGGGGCCGGGGAGTCCGCGGGGAGCGAGGGAGTTTCCGAGGGGCGGGTCGTGTTCCTGGCAGC CGAGGGGCCGGGGAGTCCGCGGGGAGCGAGGG__TTTCCGAGGGGCGGGTCGTGTTCCTGGCAGC ACT A GALE Ensembl:ENSG00000117308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:23800642..23800734;chr1:23800637..23800727 26863196 MeRIP-seq:(Medium) rs1258728172 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8166866,Human_RBP_ID_9412506,Human_RBP_ID_17646298,Human_RBP_ID_18455061,Human_RBP_ID_19037200,Human_RBP_ID_22350370,Human_RBP_ID_23255496,Human_RBP_ID_26753311,Human_RBP_ID_26773569 63843 RMVar_ID_63843 Human_SNP_ID_6362940 m1A Human chr1 - 23825310 23825306 23825310 GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTGACTGTCAGGGTTGGGGGCTTGGCCCGTGGTGAC GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTG____TCAGGGTTGGGGGCTTGGCCCGTGGTGAC ACAGT A HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23825308..23825401 26863196 MeRIP-seq:(Medium) rs1445836005 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_100637 RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 63844 RMVar_ID_63844 Human_SNP_ID_6362944 m1A Human chr1 - 23825310 23825310 23825310 GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTGACTGTCAGGGTTGGGGGCTTGGCCCGTGGTGAC GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTGCCTGTCAGGGTTGGGGGCTTGGCCCGTGGTGAC T G HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23825308..23825401 26863196 MeRIP-seq:(Medium) rs1261305769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100637 RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 63845 RMVar_ID_63845 Human_SNP_ID_6374333 m1A Human chr1 + 23868278 23868278 23868278 GCGGGACCCGCCGGCCGCGACCTCATCCCCGGAGCCCGCATCGCTACCCCTCAGCGACGCGGCCC GCGGGACCCGCCGGCCGCGACCTCATCCCCGGCGCCCGCATCGCTACCCCTCAGCGACGCGGCCC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:23868193..23868294 26863410 MeRIP-seq:(Medium) rs1265884392 Functional Loss SNV dbSNP153 33..33 33 - - - 63846 RMVar_ID_63846 Human_SNP_ID_6374334 m1A Human chr1 + 23868278 23868278 23868278 GCGGGACCCGCCGGCCGCGACCTCATCCCCGGAGCCCGCATCGCTACCCCTCAGCGACGCGGCCC GCGGGACCCGCCGGCCGCGACCTCATCCCCGGGGCCCGCATCGCTACCCCTCAGCGACGCGGCCC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:23868193..23868294 26863410 MeRIP-seq:(Medium) rs1265884392 Functional Loss SNV dbSNP153 33..33 33 - - - 63847 RMVar_ID_63847 Human_SNP_ID_6397362 m1A Human chr1 + 23959936 23959936 23959936 CTTTGTCGGTCCGTGCCTCGTCTCTCCCTGGAAAGGGAGGGAGGCTTCGACGTCGAGAGGGAGCC CTTTGTCGGTCCGTGCCTCGTCTCTCCCTGGAGAGGGAGGGAGGCTTCGACGTCGAGAGGGAGCC A G PNRC2 Ensembl:ENSG00000189266 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:23959826..23960939 26863410 MeRIP-seq:(Medium) rs1327725828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073689,Human_RBP_ID_5312381,Human_RBP_ID_5792100,Human_RBP_ID_9318704,Human_RBP_ID_22427004 Human_Splice_Rec_30847,Human_Splice_Rec_30851 RMVar_hsa_circ_121840,RMVar_hsa_circ_130516,RMVar_hsa_circ_86104,RMVar_hsa_circ_130515 63848 RMVar_ID_63848 Human_SNP_ID_6402174 m1A Human chr1 - 23980292 23980292 23980292 GCTCGGCCGCCTGAGCCGCGGACGGTTTGCTGAGCCCGTTAGTGCGCCCGGCCGAGACACGCCGC GCTCGGCCGCCTGAGCCGCGGACGGTTTGCTGGGCCCGTTAGTGCGCCCGGCCGAGACACGCCGC T C SRSF10 Ensembl:ENSG00000188529 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:23980176..23980375 26863410 MeRIP-seq:(Medium) rs1452112888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224714,Human_RBP_ID_348437,Human_RBP_ID_745748,Human_RBP_ID_1426377,Human_RBP_ID_4037637,Human_RBP_ID_8746786,Human_RBP_ID_10871975,Human_RBP_ID_18414895,Human_RBP_ID_22022955,Human_RBP_ID_23378406 RMVar_hsa_circ_11840 63849 RMVar_ID_63849 Human_SNP_ID_6450555 m1A Human chr1 - 24166452 24166449 24166453 GAAGAAAAGCAGGACATCCAGGCAGGGAAGGAAGGGCTGGAGCGAAGGAGAAGCAAGGAAGGAAG GAAGAAAAGCAGGACATCCAGGCAGGGAAGG____GCTGGAGCGAAGGAGAAGCAAGGAAGGAAG CCCTT C IFNLR1 Ensembl:ENSG00000185436 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:24166341..24166532 26863196 MeRIP-seq:(Medium) rs1426460430 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_78203,RMVar_hsa_circ_130517 63850 RMVar_ID_63850 Human_SNP_ID_6523989 m1A Human chr1 + 24472693 24472693 24472693 CTTTTCTAGTGGAAACCAGCCAGTTTGACGGCACGGTGCGGATACAGGACTCCATCAGGCTAGTG CTTTTCTAGTGGAAACCAGCCAGTTTGACGGCGCGGTGCGGATACAGGACTCCATCAGGCTAGTG A G NIPAL3 Ensembl:ENSG00000001461 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:24472577..24472827 32194978 MeRIP-seq:(Medium) rs969867972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5799412,Human_RBP_ID_8967978,Human_RBP_ID_10896167 63851 RMVar_ID_63851 Human_SNP_ID_6539017 m1A Human chr1 + 24535174 24535174 24535174 GGTTCATGTCTGTGAAAGTGAAACTGAAGAGGAAGAAGAGACAAAAAACCCCAAACAGAAAATTG GGTTCATGTCTGTGAAAGTGAAACTGAAGAGGGAGAAGAGACAAAAAACCCCAAACAGAAAATTG A G RCAN3 Ensembl:ENSG00000117602 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:24535125..24535322 26863196 MeRIP-seq:(Medium) rs140425934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1427241,Human_RBP_ID_18523100,Human_RBP_ID_18569970 Human_Splice_Rec_31538,Human_Splice_Rec_31544,Human_Splice_Rec_31552,Human_Splice_Rec_31558,Human_Splice_Rec_31564,Human_Splice_Rec_31572,Human_Splice_Rec_31580,Human_Splice_Rec_31584,Human_Splice_Rec_31588,Human_Splice_Rec_31590,Human_Splice_Rec_31592 RMVar_hsa_circ_266968 63852 RMVar_ID_63852 Human_SNP_ID_6555088 m1A Human chr1 - 24599840 24599832 24599841 CACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGGGGGGGGGGGGGGGGGGGCGGATCACGAGG CACACCTGTAATCCCAGCACTTTGGGAGGCC_________GGGGGGGGGGGGGCGGATCACGAGG CCCCCCCCTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:24599801..24599850 26863196 MeRIP-seq:(Medium) rs1557603567 Functional Loss DEL dbSNP153 32..40 33 - - - 63853 RMVar_ID_63853 Human_SNP_ID_6555095 m1A Human chr1 - 24599840 24599834 24599841 CACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGGGGGGGGGGGGGGGGGGGCGGATCACGAGG CACACCTGTAATCCCAGCACTTTGGGAGGCC_______GGGGGGGGGGGGGGGCGGATCACGAGG CCCCCCTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:24599801..24599850 26863196 MeRIP-seq:(Medium) rs60403359 Functional Loss DEL dbSNP153 32..38 33 - - - 63854 RMVar_ID_63854 Human_SNP_ID_6555106 m1A Human chr1 - 24599840 24599836 24599840 CACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGGGGGGGGGGGGGGGGGGGCGGATCACGAGG CACACCTGTAATCCCAGCACTTTGGGAGGCCA____GGGGGGGGGGGGGGGGGCGGATCACGAGG CCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:24599801..24599850 26863196 MeRIP-seq:(Medium) rs1557603598 Functional Loss DEL dbSNP153 33..36 33 - - - 63855 RMVar_ID_63855 Human_SNP_ID_6555118 m1A Human chr1 - 24599840 24599840 24599840 CACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGGGGGGGGGGGGGGGGGGGCGGATCACGAGG CACACCTGTAATCCCAGCACTTTGGGAGGCCAGGGGGGGGGGGGGGGGGGGGGCGGATCACGAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:24599801..24599850 26863196 MeRIP-seq:(Medium) rs931926543 Functional Loss SNV dbSNP153 33..33 33 - - - 63856 RMVar_ID_63856 Human_SNP_ID_6566772 m1A Human chr1 + 24643606 24643606 24643606 TGGCCGGAAAATGGCGGCGGGAATGGGCCGGGATGGTACCTCGCTGCCCGCCTGCCTGGCGGGGC TGGCCGGAAAATGGCGGCGGGAATGGGCCGGGCTGGTACCTCGCTGCCCGCCTGCCTGGCGGGGC A C SRRM1 Ensembl:ENSG00000133226 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:24643597..24643739 26863196 MeRIP-seq:(Medium) rs1327665007 Functional Loss SNV dbSNP153 33..33 33 - - - 63857 RMVar_ID_63857 Human_SNP_ID_6567485 m1A Human chr1 + 24645995 24645995 24645995 GATGTGGTTCTCTTCCTGCAGGGAACAAGTGCAGAACAGGATAATCGGTTCAGCAACAAACAGAA GATGTGGTTCTCTTCCTGCAGGGAACAAGTGCGGAACAGGATAATCGGTTCAGCAACAAACAGAA A G SRRM1 Ensembl:ENSG00000133226 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:24645976..24646050 26863196 MeRIP-seq:(Medium) rs762246291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5537611,Human_RBP_ID_9355732,Human_RBP_ID_18410087,Human_RBP_ID_18415462,Human_RBP_ID_22870772,Human_RBP_ID_24540990,Human_RBP_ID_26313601,Human_RBP_ID_26859949,Human_RBP_ID_27797555 Human_Splice_Rec_31616,Human_Splice_Rec_31617,Human_Splice_Rec_31624,Human_Splice_Rec_31625,Human_Splice_Rec_31632,Human_Splice_Rec_31633,Human_Splice_Rec_31638,Human_Splice_Rec_31639,Human_Splice_Rec_31648,Human_Splice_Rec_31649,Human_Splice_Rec_31658,Human_Splice_Rec_31659,Human_Splice_Rec_31664,Human_Splice_Rec_31665,Human_Splice_Rec_31696,Human_Splice_Rec_31697,Human_Splice_Rec_31726,Human_Splice_Rec_31727,Human_Splice_Rec_31736,Human_Splice_Rec_31737,Human_Splice_Rec_31766,Human_Splice_Rec_31767,Human_Splice_Rec_31794,Human_Splice_Rec_31795 63858 RMVar_ID_63858 Human_SNP_ID_6569282 m1A Human chr1 + 24652465 24652465 24652465 GTGACATTCTGAAAGTTCCCAAACCTGAACCTATACCAGAGCCTAAAGAACCTTCTCCGGAAAAA GTGACATTCTGAAAGTTCCCAAACCTGAACCTGTACCAGAGCCTAAAGAACCTTCTCCGGAAAAA A G SRRM1 Ensembl:ENSG00000133226 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:24652451..24652676 26863196 MeRIP-seq:(Medium) rs751330299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854129,Human_RBP_ID_1427268,Human_RBP_ID_1743775,Human_RBP_ID_5433902,Human_RBP_ID_8747361,Human_RBP_ID_9358389,Human_RBP_ID_10896606,Human_RBP_ID_17217359,Human_RBP_ID_18570014,Human_RBP_ID_22860919,Human_RBP_ID_24762975,Human_RBP_ID_26310520,Human_RBP_ID_27396554,Human_RBP_ID_27799804 Human_miRNA_ID_3067683 RMVar_hsa_circ_18621,RMVar_hsa_circ_62784,RMVar_hsa_circ_358025,RMVar_hsa_circ_267355,RMVar_hsa_circ_78311,RMVar_hsa_circ_70347,RMVar_hsa_circ_130532,RMVar_hsa_circ_365746 63859 RMVar_ID_63859 Human_SNP_ID_6569330 m1A Human chr1 - 24652564 24652564 24652564 AGTGTGAGAAGGAGAGCGGGACCGCGTCCGGGATCTTGATTTGGAGCGTGACCGAGATCGTGGTC AGTGTGAGAAGGAGAGCGGGACCGCGTCCGGGTTCTTGATTTGGAGCGTGACCGAGATCGTGGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:24652516..24652652 26863196 MeRIP-seq:(Medium) rs1557674911 Functional Loss SNV dbSNP153 33..33 33 - - - 63860 RMVar_ID_63860 Human_SNP_ID_6569348 m1A Human chr1 - 24652590 24652590 24652590 CGGGATCTATGGCGCCGTCTAGGTCGAGTGTGAGAAGGAGAGCGGGACCGCGTCCGGGATCTTGA CGGGATCTATGGCGCCGTCTAGGTCGAGTGTGGGAAGGAGAGCGGGACCGCGTCCGGGATCTTGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:24652426..24652710 26863196 MeRIP-seq:(Medium) rs748681676 Functional Loss SNV dbSNP153 33..33 33 - - - 63861 RMVar_ID_63861 Human_SNP_ID_6573281 m1A Human chr1 + 24666908 24666906 24666909 GCCCCTCCTCCTCGACGGCGCAGGACTCCCACACCACCACCACGACGAAGGTACTTTGTCAAATA GCCCCTCCTCCTCGACGGCGCAGGACTCCCA___CACCACCACGACGAAGGTACTTTGTCAAATA ACAC A SRRM1 Ensembl:ENSG00000133226 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:24666901..24666950 26863196 MeRIP-seq:(Medium) rs1326191755 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_857477,Human_RBP_ID_5799810,Human_RBP_ID_9358403,Human_RBP_ID_18570037,Human_RBP_ID_27396558 Human_Splice_Rec_31686,Human_Splice_Rec_31687,Human_Splice_Rec_31716,Human_Splice_Rec_31717,Human_Splice_Rec_31758,Human_Splice_Rec_31759,Human_Splice_Rec_31784,Human_Splice_Rec_31785,Human_Splice_Rec_31816,Human_Splice_Rec_31817,Human_Splice_Rec_31856,Human_Splice_Rec_31865 RMVar_hsa_circ_70347,RMVar_hsa_circ_365746,RMVar_hsa_circ_121590,RMVar_hsa_circ_130535,RMVar_hsa_circ_367627,RMVar_hsa_circ_289193,RMVar_hsa_circ_326607,RMVar_hsa_circ_302806,RMVar_hsa_circ_130540,RMVar_hsa_circ_105031,RMVar_hsa_circ_301620,RMVar_hsa_circ_130541 63862 RMVar_ID_63862 Human_SNP_ID_6573826 m1A Human chr1 - 24669105 24669105 24669105 GGAGGAGAAGGAGTCCTAGGAAAAAGATACATAATTAAGCTGAAAGGCTCAACAAAATACAGAAA GGAGGAGAAGGAGTCCTAGGAAAAAGATACATGATTAAGCTGAAAGGCTCAACAAAATACAGAAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:24669101..24669500 26863196 MeRIP-seq:(Medium) rs1269801272 Functional Loss SNV dbSNP153 33..33 33 - - - 63863 RMVar_ID_63863 Human_SNP_ID_6573950 m1A Human chr1 + 24669382 24669382 24669382 TATCATCCAAGCATAGGAAAGGGTCTTCCCCAAGCCGCTCTACCCGGGAGGCCCGATCACCACAA TATCATCCAAGCATAGGAAAGGGTCTTCCCCAGGCCGCTCTACCCGGGAGGCCCGATCACCACAA A G SRRM1 Ensembl:ENSG00000133226 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:24669051..24669509 26863196 MeRIP-seq:(Medium) rs565269582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_859852,Human_RBP_ID_9355745,Human_RBP_ID_17217369,Human_RBP_ID_17334828,Human_RBP_ID_24541016,Human_RBP_ID_26310531,Human_RBP_ID_27797585 RMVar_hsa_circ_365746,RMVar_hsa_circ_121590,RMVar_hsa_circ_130535,RMVar_hsa_circ_367627,RMVar_hsa_circ_326607,RMVar_hsa_circ_301620 63864 RMVar_ID_63864 Human_SNP_ID_6594436 m1A Human chr1 + 24745515 24745515 24745515 AGCAGTCCCGGAGCAGAAGCAGCAGCAGCAGCAGCAGCCCTCGCCGTTCGCGGAGCGCAGCCGAG AGCAGTCCCGGAGCAGAAGCAGCAGCAGCAGCGGCAGCCCTCGCCGTTCGCGGAGCGCAGCCGAG A G CLIC4 Ensembl:ENSG00000169504 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:24745415..24745545 26863410 MeRIP-seq:(Medium) rs775132364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224539,Human_RBP_ID_4092793,Human_RBP_ID_5312382,Human_RBP_ID_17337986 63865 RMVar_ID_63865 Human_SNP_ID_6598849 m1A Human chr1 + 24762442 24762442 24762442 ACTCTCTCTAAAGAAAAAAACAAGTGTATGAGATCATTGTGTGGATGAGTAAAGAGTGAGGAAAA ACTCTCTCTAAAGAAAAAAACAAGTGTATGAGGTCATTGTGTGGATGAGTAAAGAGTGAGGAAAA A G CLIC4 Ensembl:ENSG00000169504 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:24762440..24762875 26863196 MeRIP-seq:(Medium) rs1251462513 Functional Loss SNV dbSNP153 33..33 33 - - - 63866 RMVar_ID_63866 Human_SNP_ID_6611851 m1A Human chr1 - 24814079 24814079 24814079 TGCAGGTCTGCTGGCTTCCTGTTGGGCAAAATATTGGTCAAAATCAGATCATTTTTTACTCTTAA TGCAGGTCTGCTGGCTTCCTGTTGGGCAAAATGTTGGTCAAAATCAGATCATTTTTTACTCTTAA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr1:24814076..24814100;chr1:24814076..24814225 26863196,32194978 MeRIP-seq:(Medium) rs878868397 Functional Loss SNV dbSNP153 33..33 33 - - - 63867 RMVar_ID_63867 Human_SNP_ID_6611874 m1A Human chr1 + 24814143 24814143 24814143 AGAACTTGGCTCCCGGGACCCACCCACCATTTATAACTTTCAACAGTGAAGTCAAAACGGATGTA AGAACTTGGCTCCCGGGACCCACCCACCATTTGTAACTTTCAACAGTGAAGTCAAAACGGATGTA A G CLIC4 Ensembl:ENSG00000169504 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:24814126..24814200 26863196 MeRIP-seq:(Medium) rs201465229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22929,Human_RBP_ID_5485927,Human_RBP_ID_9268466,Human_RBP_ID_17217382,Human_RBP_ID_17334837,Human_RBP_ID_17746821,Human_RBP_ID_18523109,Human_RBP_ID_22487649,Human_RBP_ID_27592265 Human_Splice_Rec_31880,Human_Splice_Rec_31881,Human_Splice_Rec_31888,Human_Splice_Rec_31889,Human_Splice_Rec_31900,Human_Splice_Rec_31901 Human_miRNA_ID_643982,Human_miRNA_ID_987932,Human_miRNA_ID_2245991,Human_miRNA_ID_2850297,Human_miRNA_ID_2975936 RMVar_hsa_circ_236,RMVar_hsa_circ_13736,RMVar_hsa_circ_130543,RMVar_hsa_circ_279677,RMVar_hsa_circ_290593,RMVar_hsa_circ_350165,RMVar_hsa_circ_37651,RMVar_hsa_circ_320843 63868 RMVar_ID_63868 Human_SNP_ID_6632854 m1A Human chr1 - 24901671 24901663 24901672 CCCGACCCCTGCACCTTCGTTGGAGCCCCTGCATCCCCTGGGTCCAGCCCCCTCTGCATTTACAC CCCGACCCCTGCACCTTCGTTGGAGCCCCTG_________GGTCCAGCCCCCTCTGCATTTACAC CCAGGGGATG C RUNX3 Ensembl:ENSG00000020633 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:24901620..24901747 26863196 MeRIP-seq:(Medium) rs1274446607 Functional Loss DEL dbSNP153 32..40 33 - - - 63869 RMVar_ID_63869 Human_SNP_ID_6716567 m1A Human chr1 - 25229076 25229076 25229076 TTAAATCACCAGGAAGTTGTGGAAGAAGATAAAAGACTAAAATTACCTGCAAATTGGGAAGCCAA TTAAATCACCAGGAAGTTGTGGAAGAAGATAACAGACTAAAATTACCTGCAAATTGGGAAGCCAA T G SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:25229026..25229075 32194978 MeRIP-seq:(Medium) rs1355356083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24541,Human_RBP_ID_1427410,Human_RBP_ID_1743870,Human_RBP_ID_4039993,Human_RBP_ID_22860995,Human_RBP_ID_26310545,Human_RBP_ID_27799841 Human_Splice_Rec_31970,Human_Splice_Rec_31971,Human_Splice_Rec_31990 RMVar_hsa_circ_52219,RMVar_hsa_circ_67009 63870 RMVar_ID_63870 Human_SNP_ID_6716580 m1A Human chr1 - 25229122 25229122 25229122 AGCTGACAGACTTCTTGTGTTACGGTTTTAGAATGAAGCTCGTAAATTAAATCACCAGGAAGTTG AGCTGACAGACTTCTTGTGTTACGGTTTTAGAGTGAAGCTCGTAAATTAAATCACCAGGAAGTTG T C SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25228944..25229176 26863196 MeRIP-seq:(Medium) rs764065825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_31970,Human_Splice_Rec_31990 RMVar_hsa_circ_52219,RMVar_hsa_circ_67009 63871 RMVar_ID_63871 Human_SNP_ID_6717491 m1A Human chr1 - 25232150 25232150 25232150 CCTCGCTGCGGCGGCGGAGCTGGCCGCTCAGAAGCGCGAACAGAGACTGCGCAAATTCCGGGAGC CCTCGCTGCGGCGGCGGAGCTGGCCGCTCAGATGCGCGAACAGAGACTGCGCAAATTCCGGGAGC T A SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:25232101..25232247 26863196 MeRIP-seq:(Medium) rs1409589861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_349848,Human_RBP_ID_4073694,Human_RBP_ID_22022959,Human_RBP_ID_26310548,Human_RBP_ID_27797602 Human_Splice_Rec_31968,Human_Splice_Rec_31969,Human_Splice_Rec_31980,Human_Splice_Rec_31981,Human_Splice_Rec_31989,Human_Splice_Rec_31992 63872 RMVar_ID_63872 Human_SNP_ID_6741685 m1A Human chr1 - 25338004 25338004 25338004 GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGAGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGGGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT T C RSRP1 Ensembl:ENSG00000117616 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25337992..25338104 26863196 MeRIP-seq:(Medium) rs585500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22707042,Human_RBP_ID_24359574,Human_RBP_ID_26772990,Human_RBP_ID_27571565 Human_Splice_Rec_32077 63873 RMVar_ID_63873 Human_SNP_ID_6741686 m1A Human chr1 - 25338004 25338004 25338004 GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGAGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGCGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT T G RSRP1 Ensembl:ENSG00000117616 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25337992..25338104 26863196 MeRIP-seq:(Medium) rs585500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22707042,Human_RBP_ID_24359574,Human_RBP_ID_26772990,Human_RBP_ID_27571565 Human_Splice_Rec_32077 63874 RMVar_ID_63874 Human_SNP_ID_6741807 m1A Human chr1 + 25338356 25338356 25338356 GGTGGATGGTACTGCTGCATCCGGGTGTCTGGAGGCTGTGGCCGTTTTGTTTTCTTGGCTAAAAT GGTGGATGGTACTGCTGCATCCGGGTGTCTGGCGGCTGTGGCCGTTTTGTTTTCTTGGCTAAAAT A C TMEM50A Ensembl:ENSG00000183726 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:25338326..25338455 26863196 MeRIP-seq:(Medium) rs991441770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102843,Human_RBP_ID_4040035,Human_RBP_ID_5800717,Human_RBP_ID_8306463,Human_RBP_ID_10898834,Human_RBP_ID_23382749 63875 RMVar_ID_63875 Human_SNP_ID_6742352 m1A Human chr1 - 25340523 25340523 25340523 AATAGTATTGCGCTTTTCCCCCCAGTCAATGCATTCTGAGCATCTCAAGCCCTCTAGAAATCCAG AATAGTATTGCGCTTTTCCCCCCAGTCAATGCCTTCTGAGCATCTCAAGCCCTCTAGAAATCCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:25340429..25340550;chr1:25340412..25340550;chr1:25340409..25340525 26863196 MeRIP-seq:(Medium) rs772741947 Functional Loss SNV dbSNP153 33..33 33 - - - 63876 RMVar_ID_63876 Human_SNP_ID_6742384 m1A Human chr1 - 25340581 25340578 25340582 AAAAAATAAGGCCCAAATAATCAATGACACTTACTAGTACACCAGCAGCAATGGAAGCAATAGTA AAAAAATAAGGCCCAAATAATCAATGACACT____AGTACACCAGCAGCAATGGAAGCAATAGTA TAGTA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:25338759..25342626 32194978 MeRIP-seq:(Medium) rs1291751332 Functional Loss DEL dbSNP153 32..35 33 - - - 63877 RMVar_ID_63877 Human_SNP_ID_6763588 m1A Human chr1 + 25431078 25431078 25431078 CTGAGGTGAGAGACGGCGGCGGCGGCGCGGGCACCCGGCCCCCCAGCGGGAGGATGAAGCGGCGG CTGAGGTGAGAGACGGCGGCGGCGGCGCGGGCCCCCGGCCCCCCAGCGGGAGGATGAAGCGGCGG A C MACO1 Ensembl:ENSG00000204178 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:25430966..25431130 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4040127,Human_RBP_ID_9319813 63878 RMVar_ID_63878 Human_SNP_ID_6778381 m1A Human chr1 + 25492414 25492411 25492414 CAGGGCAATCATGGAAAATCCCTTGAGTAGGTAGTATTTGAGCAGAGACCCAAAGGAAGAGAGCA CAGGGCAATCATGGAAAATCCCTTGAGTAG___GTATTTGAGCAGAGACCCAAAGGAAGAGAGCA GGTA G MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:25492408..25492632 26863196 MeRIP-seq:(Medium) rs1440391999 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_10899457 63879 RMVar_ID_63879 Human_SNP_ID_6790565 m1A Human chr1 + 25543786 25543786 25543786 AGCAGAGCTGGGGGGGCGGTGGCCGGCACCGCAGTGAGTGTGCGCGCGTCAGCCGGGCCGGGCCG AGCAGAGCTGGGGGGGCGGTGGCCGGCACCGCGGTGAGTGTGCGCGCGTCAGCCGGGCCGGGCCG A G LDLRAP1 Ensembl:ENSG00000157978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25543618..25550097 26863196 MeRIP-seq:(Medium) rs908146098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_32503 63880 RMVar_ID_63880 Human_SNP_ID_6790619 m1A Human chr1 + 25543937 25543937 25543937 CCCGGCGTGGCCCTTTCCCGGCCCTGCGGGGCAGGGGGTCGGCCGGGGTCAAGTTGTGCACCTAC CCCGGCGTGGCCCTTTCCCGGCCCTGCGGGGCCGGGGGTCGGCCGGGGTCAAGTTGTGCACCTAC A C LDLRAP1 Ensembl:ENSG00000157978 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:25543931..25544044 26863196 MeRIP-seq:(Medium) rs538814423 Functional Loss SNV dbSNP153 33..33 33 - - - 63881 RMVar_ID_63881 Human_SNP_ID_6792250 m1A Human chr1 - 25550722 25550722 25550722 AGGCCCTCAGCTCAAGCCCCTCACTTGATGATACAACTGAAGCCCAGACAGGGATGGGACCTGTG AGGCCCTCAGCTCAAGCCCCTCACTTGATGATGCAACTGAAGCCCAGACAGGGATGGGACCTGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:25550717..25551047 26863196 MeRIP-seq:(Medium) rs1196565239 Functional Loss SNV dbSNP153 33..33 33 - - - 63882 RMVar_ID_63882 Human_SNP_ID_6852883 m1A Human chr1 + 25800267 25800267 25800267 GCCGGGCCCGGCCGGGCCAACGCGGGCCGCCCAGCCCCGGCCCCGCCGCGCAGCCTCCCGCGCCA GCCGGGCCCGGCCGGGCCAACGCGGGCCGCCCGGCCCCGGCCCCGCCGCGCAGCCTCCCGCGCCA A G SELENON Ensembl:ENSG00000162430 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25800223..25800508 26863196 MeRIP-seq:(Medium) rs112727286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4040287 Human_miRNA_ID_2145873,Human_miRNA_ID_2987308,Human_miRNA_ID_3020998,Human_miRNA_ID_3065298 RMVar_hsa_circ_114934,RMVar_hsa_circ_130585 63883 RMVar_ID_63883 Human_SNP_ID_6853042 m1A Human chr1 - 25800715 25800715 25800715 TGTGTCCCCTCCTCACTGTCCCAGGGCTCCCCAGTAACCCTTTAAGACTCTGCGGGAACCAGCTT TGTGTCCCCTCCTCACTGTCCCAGGGCTCCCCGGTAACCCTTTAAGACTCTGCGGGAACCAGCTT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:25800648..25800828 26863196 MeRIP-seq:(Medium) rs1221551295 Functional Loss SNV dbSNP153 33..33 33 - - - 63884 RMVar_ID_63884 Human_SNP_ID_6853046 m1A Human chr1 + 25800743 25800743 25800743 TTACTGGGGAGCCCTGGGACAGTGAGGAGGGGACACAGGAGAGGACAGAAGGTGCAGGAGGAACA TTACTGGGGAGCCCTGGGACAGTGAGGAGGGGCCACAGGAGAGGACAGAAGGTGCAGGAGGAACA A C SELENON Ensembl:ENSG00000162430 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25800738..25800881 26863196 MeRIP-seq:(Medium) rs1221211996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114934,RMVar_hsa_circ_130585 63885 RMVar_ID_63885 Human_SNP_ID_6854263 m1A Human chr1 - 25805185 25805183 25805185 GCTTCTATGGTGAGCGTCTCCTCGCTAGGGTCAGGGGGCAACTCCTCCTCCTCGCAGCTGGCCGC GCTTCTATGGTGAGCGTCTCCTCGCTAGGGTC__GGGGCAACTCCTCCTCCTCGCAGCTGGCCGC CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:25800374..25808584 32194978 MeRIP-seq:(Medium) rs1192828749 Functional Loss DEL dbSNP153 33..34 33 - - - 63886 RMVar_ID_63886 Human_SNP_ID_6854264 m1A Human chr1 - 25805185 25805184 25805185 GCTTCTATGGTGAGCGTCTCCTCGCTAGGGTCAGGGGGCAACTCCTCCTCCTCGCAGCTGGCCGC GCTTCTATGGTGAGCGTCTCCTCGCTAGGGTC_GGGGGCAACTCCTCCTCCTCGCAGCTGGCCGC CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:25800374..25808584 32194978 MeRIP-seq:(Medium) rs775625468 Functional Loss DEL dbSNP153 33..33 33 - - - 63887 RMVar_ID_63887 Human_SNP_ID_6855203 m1A Human chr1 + 25808649 25808649 25808649 CAGCCGCCGCCTCACCAAGTGCAGTGTTTGCCACCCGCCACTTCCAGCCCTTCCTTCCCCCGCCA CAGCCGCCGCCTCACCAAGTGCAGTGTTTGCCCCCCGCCACTTCCAGCCCTTCCTTCCCCCGCCA A C SELENON Ensembl:ENSG00000162430 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:25808576..25808736;chr1:25808574..25808726 26863196 MeRIP-seq:(Medium) rs752463295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4040304,Human_RBP_ID_23382945 Human_Splice_Rec_32670,Human_Splice_Rec_32696,Human_Splice_Rec_32718 RMVar_hsa_circ_6205,RMVar_hsa_circ_35596,RMVar_hsa_circ_105872,RMVar_hsa_circ_114934,RMVar_hsa_circ_364975,RMVar_hsa_circ_130585,RMVar_hsa_circ_322366,RMVar_hsa_circ_17014,RMVar_hsa_circ_18474,RMVar_hsa_circ_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586,RMVar_hsa_circ_44592,RMVar_hsa_circ_130590,RMVar_hsa_circ_102700,RMVar_hsa_circ_331113,RMVar_hsa_circ_85638,RMVar_hsa_circ_130591,RMVar_hsa_circ_130589 63888 RMVar_ID_63888 Human_SNP_ID_6857847 m1A Human chr1 + 25817043 25817043 25817043 TTAAGGTCTTGAAGTCAGGCTGCCCCCTCCCCAGCCCCCAGTTCTCTCCCCACCCCCTCACCCCA TTAAGGTCTTGAAGTCAGGCTGCCCCCTCCCCCGCCCCCAGTTCTCTCCCCACCCCCTCACCCCA A C SELENON,AL020996.2 Ensembl:ENSG00000162430,Ensembl:ENSG00000255054 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25816997..25817142 26863196 MeRIP-seq:(Medium) rs1372816667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350006,Human_RBP_ID_5136133,Human_RBP_ID_5801152,Human_RBP_ID_10899821,Human_RBP_ID_17072299,Human_RBP_ID_17217506 Human_miRNA_ID_841305,Human_miRNA_ID_1355181,Human_miRNA_ID_2071751,Human_miRNA_ID_2073431,Human_miRNA_ID_2135309,Human_miRNA_ID_2365679,Human_miRNA_ID_2365680,Human_miRNA_ID_2664111,Human_miRNA_ID_2682635,Human_miRNA_ID_2724593,Human_miRNA_ID_3013485,Human_miRNA_ID_3063592 RMVar_hsa_circ_114934,RMVar_hsa_circ_130585,RMVar_hsa_circ_85638,RMVar_hsa_circ_130591,RMVar_hsa_circ_103238,RMVar_hsa_circ_130595 63889 RMVar_ID_63889 Human_SNP_ID_6858848 m1A Human chr1 - 25820010 25820009 25820010 GAACCTTTCTCACCTCAAGCTCGGGCTCCCGGACTCTCTCACCTCACGGCCCCTCCTTCCACCTT GAACCTTTCTCACCTCAAGCTCGGGCTCCCGG_CTCTCTCACCTCACGGCCCCTCCTTCCACCTT GT G AL020996.1 Ensembl:ENSG00000228172 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25819961..25820110 26863196 MeRIP-seq:(Medium) rs1393916276 Functional Loss DEL dbSNP153 33..33 33 - - - 63890 RMVar_ID_63890 Human_SNP_ID_6858863 m1A Human chr1 - 25820026 25820026 25820026 CCTCCGCGCCTCCCTAGAACCTTTCTCACCTCAAGCTCGGGCTCCCGGACTCTCTCACCTCACGG CCTCCGCGCCTCCCTAGAACCTTTCTCACCTCTAGCTCGGGCTCCCGGACTCTCTCACCTCACGG T A AL020996.1 Ensembl:ENSG00000228172 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:25820011..25820110 26863410 MeRIP-seq:(Medium) rs954362539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5539263 63891 RMVar_ID_63891 Human_SNP_ID_6859075 m1A Human chr1 + 25820555 25820554 25820555 GCGCGGCGGCCTCCGTGGGGGCCCCCGGGACCAGGGGTGCTGAGCAGGGCCCTGCGCTGGAGGAG GCGCGGCGGCCTCCGTGGGGGCCCCCGGGACC_GGGGTGCTGAGCAGGGCCCTGCGCTGGAGGAG CA C MTFR1L,AL020996.2 Ensembl:ENSG00000117640,Ensembl:ENSG00000255054 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25820551..25820699 26863196 MeRIP-seq:(Medium) rs1457489752 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18473816,Human_RBP_ID_22469250 63892 RMVar_ID_63892 Human_SNP_ID_6859803 m1A Human chr1 + 25823104 25823104 25823104 TGCCTTGTCCTTCAAGTGCAGGAGCTGGTTCAAATGTCAGGAATGGAAGCCACTGTGGTAAGGGG TGCCTTGTCCTTCAAGTGCAGGAGCTGGTTCAGATGTCAGGAATGGAAGCCACTGTGGTAAGGGG A G LOC646471 RNACentral:URS000075A9AE lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs574213756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10899868 63893 RMVar_ID_63893 Human_SNP_ID_6859804 m1A Human chr1 + 25823104 25823104 25823104 TGCCTTGTCCTTCAAGTGCAGGAGCTGGTTCAAATGTCAGGAATGGAAGCCACTGTGGTAAGGGG TGCCTTGTCCTTCAAGTGCAGGAGCTGGTTCATATGTCAGGAATGGAAGCCACTGTGGTAAGGGG A T LOC646471 RNACentral:URS000075A9AE lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs574213756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10899868 63894 RMVar_ID_63894 Human_SNP_ID_6860517 m1A Human chr1 - 25826085 25826085 25826085 TCACACCTGTAATCCCAGCATTTGGGAGGCCGAGGCAGGCAGAATGCTTGAGACCAAGAGTTTGA TCACACCTGTAATCCCAGCATTTGGGAGGCCGGGGCAGGCAGAATGCTTGAGACCAAGAGTTTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:25826082..25826183 32194978 MeRIP-seq:(Medium) rs555488040 Functional Loss SNV dbSNP153 33..33 33 - - - 63895 RMVar_ID_63895 Human_SNP_ID_6863204 m1A Human chr1 - 25835756 25835756 25835756 CAAAGAGTCCAAGAAAAATGCGACCCAGCTAGACCATTTGATCCCAGGCTTAGCACACGATTGCA CAAAGAGTCCAAGAAAAATGCGACCCAGCTAGGCCATTTGATCCCAGGCTTAGCACACGATTGCA T C AUNIP Ensembl:ENSG00000127423 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25835706..25835771 26863196 MeRIP-seq:(Medium) rs1333857136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3308148,Human_RBP_ID_5801239,Human_RBP_ID_10900106 Human_Splice_Rec_32986,Human_Splice_Rec_32994 Human_miRNA_ID_2245992,Human_miRNA_ID_2850298 RMVar_hsa_circ_83452,RMVar_hsa_circ_130597,RMVar_hsa_circ_354911 63896 RMVar_ID_63896 Human_SNP_ID_6868596 m1A Human chr1 + 25859320 25859320 25859320 TCCGCCTCTTCAGCGCCGCCGCGTCCAGCCACACGCCGCAGGCCTCCTCCTCGGGGCCTGTCCGC TCCGCCTCTTCAGCGCCGCCGCGTCCAGCCACGCGCCGCAGGCCTCCTCCTCGGGGCCTGTCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25859205..25859401 26863196 MeRIP-seq:(Medium) rs1489047687 Functional Loss SNV dbSNP153 33..33 33 - - - 63897 RMVar_ID_63897 Human_SNP_ID_6868597 m1A Human chr1 + 25859320 25859320 25859320 TCCGCCTCTTCAGCGCCGCCGCGTCCAGCCACACGCCGCAGGCCTCCTCCTCGGGGCCTGTCCGC TCCGCCTCTTCAGCGCCGCCGCGTCCAGCCACTCGCCGCAGGCCTCCTCCTCGGGGCCTGTCCGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25859205..25859401 26863196 MeRIP-seq:(Medium) rs1489047687 Functional Loss SNV dbSNP153 33..33 33 - - - 63898 RMVar_ID_63898 Human_SNP_ID_6868602 m1A Human chr1 - 25859332 25859329 25859332 AGCGGCCATGAGGCGGACAGGCCCCGAGGAGGAGGCCTGCGGCGTGTGGCTGGACGCGGCGGCGC AGCGGCCATGAGGCGGACAGGCCCCGAGGAGG___CCTGCGGCGTGTGGCTGGACGCGGCGGCGC GCCT G AUNIP Ensembl:ENSG00000127423 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:25859058..25859397 26863196 MeRIP-seq:(Medium) rs1557458758 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_223880,Human_RBP_ID_4073710 Human_Splice_Rec_32983,Human_Splice_Rec_32991 63899 RMVar_ID_63899 Human_SNP_ID_6869681 m1A Human chr1 - 25862950 25862950 25862950 GCTGGCTCAGCTGGAGGCTGTGGCACTGGACTATGAGGCCCGACGGCCCATCTATGAGCCTCTGC GCTGGCTCAGCTGGAGGCTGTGGCACTGGACTGTGAGGCCCGACGGCCCATCTATGAGCCTCTGC T C PAQR7 Ensembl:ENSG00000182749 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:25862857..25862958 32194978 MeRIP-seq:(Medium) rs1203385137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17223309,Human_RBP_ID_22751741,Human_RBP_ID_27396671 RMVar_hsa_circ_112344,RMVar_hsa_circ_130598 63900 RMVar_ID_63900 Human_SNP_ID_6869919 m1A Human chr1 - 25863607 25863607 25863607 GCAGCACAACGAGGCCGTGAATGTCTGGACCCACCTGCTGGCGGCCCTGGTACTGCTGCTGCGGC GCAGCACAACGAGGCCGTGAATGTCTGGACCCCCCTGCTGGCGGCCCTGGTACTGCTGCTGCGGC T G PAQR7 Ensembl:ENSG00000182749 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:25863556..25863707 32194978 MeRIP-seq:(Medium) rs1256331333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075292 Human_miRNA_ID_2219223,Human_miRNA_ID_2482260,Human_miRNA_ID_2571732,Human_miRNA_ID_3070637 RMVar_hsa_circ_112344,RMVar_hsa_circ_130598 63901 RMVar_ID_63901 Human_SNP_ID_6870023 m1A Human chr1 - 25863803 25863803 25863803 CCATGGCCCAGAAACTCAGCCACCTCCTGCCGAGTCTGCGGCAGGTCATCCAGGAGCCTCAGCTA CCATGGCCCAGAAACTCAGCCACCTCCTGCCGGGTCTGCGGCAGGTCATCCAGGAGCCTCAGCTA T C PAQR7 Ensembl:ENSG00000182749 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:25863756..25870704 32194978 MeRIP-seq:(Medium) rs1358486324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_32998 RMVar_hsa_circ_112344,RMVar_hsa_circ_130598 63902 RMVar_ID_63902 Human_SNP_ID_6870050 m1A Human chr1 + 25863856 25863856 25863856 TCTGGGCCATGGCCATGGCTGTGGGCCTGGGCAGGGAGCTGGGAGAGAGACCAGAGCAAAGTCAG TCTGGGCCATGGCCATGGCTGTGGGCCTGGGCGGGGAGCTGGGAGAGAGACCAGAGCAAAGTCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:25863806..25870654 32194978 MeRIP-seq:(Medium) rs1209298281 Functional Loss SNV dbSNP153 33..33 33 - - - 63903 RMVar_ID_63903 Human_SNP_ID_6879080 m1A Human chr1 - 25901601 25901601 25901601 AGAAAGAAGTGCTTCAGAAGGCAATAGAAGAGAACAACAACTTCAGTAAAATGGCAGAAGAGAAA AGAAAGAAGTGCTTCAGAAGGCAATAGAAGAGGACAACAACTTCAGTAAAATGGCAGAAGAGAAA T C STMN1 Ensembl:ENSG00000117632 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:25901474..25901630 26863196 MeRIP-seq:(Medium) rs11538124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24583,Human_RBP_ID_350137,Human_RBP_ID_977116,Human_RBP_ID_1427506,Human_RBP_ID_1744000,Human_RBP_ID_3308177,Human_RBP_ID_5801382,Human_RBP_ID_9355768,Human_RBP_ID_10900369,Human_RBP_ID_17217542,Human_RBP_ID_18430011,Human_RBP_ID_23383053,Human_RBP_ID_24541437,Human_RBP_ID_26309680,Human_RBP_ID_26860291 Human_Splice_Rec_33006,Human_Splice_Rec_33014,Human_Splice_Rec_33022,Human_Splice_Rec_33036,Human_Splice_Rec_33044,Human_Splice_Rec_33048,Human_Splice_Rec_33054 RMVar_hsa_circ_130606,RMVar_hsa_circ_130603,RMVar_hsa_circ_268731,RMVar_hsa_circ_130604,RMVar_hsa_circ_338323,RMVar_hsa_circ_130607,RMVar_hsa_circ_130605 63904 RMVar_ID_63904 Human_SNP_ID_6879549 m1A Human chr1 - 25903743 25903743 25903743 CAGGCTTTTGAGCTGATTCTCAGCCCTCGGTCAAAAGAATCTGTTCCAGAATTCCCCCTTTCCCC CAGGCTTTTGAGCTGATTCTCAGCCCTCGGTCGAAAGAATCTGTTCCAGAATTCCCCCTTTCCCC T C STMN1 Ensembl:ENSG00000117632 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25903692..25903775 26863196 MeRIP-seq:(Medium) rs765208355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24589,Human_RBP_ID_273427,Human_RBP_ID_350145,Human_RBP_ID_977120,Human_RBP_ID_1427517,Human_RBP_ID_1744006,Human_RBP_ID_3308189,Human_RBP_ID_4040595,Human_RBP_ID_5433912,Human_RBP_ID_5801416,Human_RBP_ID_8306572,Human_RBP_ID_8968198,Human_RBP_ID_9355774,Human_RBP_ID_9510943,Human_RBP_ID_10900441,Human_RBP_ID_17451970,Human_RBP_ID_18570286,Human_RBP_ID_22429159,Human_RBP_ID_23383062,Human_RBP_ID_24541775,Human_RBP_ID_24763131,Human_RBP_ID_27180079,Human_RBP_ID_27396687 Human_Splice_Rec_33004,Human_Splice_Rec_33012,Human_Splice_Rec_33020,Human_Splice_Rec_33028,Human_Splice_Rec_33034,Human_Splice_Rec_33042,Human_Splice_Rec_33052 RMVar_hsa_circ_338323,RMVar_hsa_circ_130607,RMVar_hsa_circ_130608,RMVar_hsa_circ_338197 63905 RMVar_ID_63905 Human_SNP_ID_6879799 m1A Human chr1 + 25904714 25904714 25904714 ATAGAAGACAAGCGACAGGCAGTGTATTCTGCACAATCAACTGGGATAAGGAAAGTCCTGAAAAT ATAGAAGACAAGCGACAGGCAGTGTATTCTGCGCAATCAACTGGGATAAGGAAAGTCCTGAAAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:25904651..25904750 32194978 MeRIP-seq:(Medium) rs745950078 Functional Loss SNV dbSNP153 33..33 33 - - - 63906 RMVar_ID_63906 Human_SNP_ID_6880101 m1A Human chr1 + 25905716 25905716 25905716 GCCTGACTCCCCCTGCGCGGACGCCCCCCCCAACTCCCGCCAAAAACACCTCCAGGCCGCCGCCA GCCTGACTCCCCCTGCGCGGACGCCCCCCCCAGCTCCCGCCAAAAACACCTCCAGGCCGCCGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:25905712..25905933 26863196 MeRIP-seq:(Medium) rs926332795 Functional Loss SNV dbSNP153 33..33 33 - - - 63907 RMVar_ID_63907 Human_SNP_ID_6880102 m1A Human chr1 + 25905716 25905716 25905716 GCCTGACTCCCCCTGCGCGGACGCCCCCCCCAACTCCCGCCAAAAACACCTCCAGGCCGCCGCCA GCCTGACTCCCCCTGCGCGGACGCCCCCCCCATCTCCCGCCAAAAACACCTCCAGGCCGCCGCCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:25905712..25905933 26863196 MeRIP-seq:(Medium) rs926332795 Functional Loss SNV dbSNP153 33..33 33 - - - 63908 RMVar_ID_63908 Human_SNP_ID_6880268 m1A Human chr1 + 25906137 25906137 25906137 CGCCCCCTATTGTCTCCTCGACGGCACCCCGGAGCGGACGCCCGGTGATCGCCCAGCCCCCTGCC CGCCCCCTATTGTCTCCTCGACGGCACCCCGGGGCGGACGCCCGGTGATCGCCCAGCCCCCTGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:25906132..25906425 26863196 MeRIP-seq:(Medium) rs975835780 Functional Loss SNV dbSNP153 33..33 33 - - - 63909 RMVar_ID_63909 Human_SNP_ID_6880287 m1A Human chr1 + 25906191 25906191 25906191 AGCCCCCTGCCCACGAACAGCCGCGCCCCCGGAGAGCGGGGACAAAGGCGAGGCTCCGCCCGAGC AGCCCCCTGCCCACGAACAGCCGCGCCCCCGGCGAGCGGGGACAAAGGCGAGGCTCCGCCCGAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:25906188..25906425 26863196 MeRIP-seq:(Medium) rs945220888 Functional Loss SNV dbSNP153 33..33 33 - - - 63910 RMVar_ID_63910 Human_SNP_ID_6931123 m1A Human chr1 - 26111216 26111216 26111216 CCGAGTCACTGAGCCATGTTTGCGGGCGGTGCAGTTGCGGAGACGGCGGCGGCGGCGGCGGCGCG CCGAGTCACTGAGCCATGTTTGCGGGCGGTGCGGTTGCGGAGACGGCGGCGGCGGCGGCGGCGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26111165..26111366 26863196 MeRIP-seq:(Medium) rs970228342 Functional Loss SNV dbSNP153 33..33 33 - - - 63911 RMVar_ID_63911 Human_SNP_ID_6931385 m1A Human chr1 + 26111883 26111883 26111883 GAGCTGCCCGATAATGGCGGCCTGCAGAGCCCATGAGAGGGAGAAGCGGCAGCGTCTACCCTGAG GAGCTGCCCGATAATGGCGGCCTGCAGAGCCCGTGAGAGGGAGAAGCGGCAGCGTCTACCCTGAG A G PDIK1L Ensembl:ENSG00000175087 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26111832..26111958 26863196 MeRIP-seq:(Medium) rs1053872121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073721,Human_RBP_ID_8754847 Human_Splice_Rec_33231,Human_Splice_Rec_33235 63912 RMVar_ID_63912 Human_SNP_ID_6931388 m1A Human chr1 + 26111888 26111888 26111888 GCCCGATAATGGCGGCCTGCAGAGCCCATGAGAGGGAGAAGCGGCAGCGTCTACCCTGAGGTAAA GCCCGATAATGGCGGCCTGCAGAGCCCATGAGCGGGAGAAGCGGCAGCGTCTACCCTGAGGTAAA A C PDIK1L Ensembl:ENSG00000175087 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26111846..26111913 26863196 MeRIP-seq:(Medium) rs1005523974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073721,Human_RBP_ID_8754847 Human_Splice_Rec_33231,Human_Splice_Rec_33235 63913 RMVar_ID_63913 Human_SNP_ID_6945231 m1A Human chr1 + 26170151 26170151 26170151 GACCCAAACGCCGAGTTCGACCCCGACCTGCCAGGGGGCGGTCTGCACCGCTGTCTGGCCTGCGC GACCCAAACGCCGAGTTCGACCCCGACCTGCCGGGGGGCGGTCTGCACCGCTGTCTGGCCTGCGC A G ZNF593 Ensembl:ENSG00000142684 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:26170105..26170253 32194978 MeRIP-seq:(Medium) rs765856781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742990,Human_RBP_ID_22427017,Human_RBP_ID_26797933 Human_Splice_Rec_33275,Human_Splice_Rec_33279 RMVar_hsa_circ_130616,RMVar_hsa_circ_105822 63914 RMVar_ID_63914 Human_SNP_ID_6945232 m1A Human chr1 + 26170151 26170151 26170151 GACCCAAACGCCGAGTTCGACCCCGACCTGCCAGGGGGCGGTCTGCACCGCTGTCTGGCCTGCGC GACCCAAACGCCGAGTTCGACCCCGACCTGCCTGGGGGCGGTCTGCACCGCTGTCTGGCCTGCGC A T ZNF593 Ensembl:ENSG00000142684 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:26170105..26170253 32194978 MeRIP-seq:(Medium) rs765856781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742990,Human_RBP_ID_22427017,Human_RBP_ID_26797933 Human_Splice_Rec_33275,Human_Splice_Rec_33279 RMVar_hsa_circ_130616,RMVar_hsa_circ_105822 63915 RMVar_ID_63915 Human_SNP_ID_6947177 m1A Human chr1 + 26177579 26177579 26177579 CATGGAACCGGTAGAGACCTGGACCCCCGGAAAGGTGGCAACTTGGCTGAGAGGTGGGTGGGGCT CATGGAACCGGTAGAGACCTGGACCCCCGGAAGGGTGGCAACTTGGCTGAGAGGTGGGTGGGGCT A G CNKSR1 Ensembl:ENSG00000142675 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26177530..26177647 26863196 MeRIP-seq:(Medium) rs201291243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18965046 Human_Splice_Rec_33281,Human_Splice_Rec_33297,Human_Splice_Rec_33309,Human_Splice_Rec_33349,Human_Splice_Rec_33353,Human_Splice_Rec_33393,Human_Splice_Rec_33417 63916 RMVar_ID_63916 Human_SNP_ID_6947178 m1A Human chr1 + 26177579 26177579 26177579 CATGGAACCGGTAGAGACCTGGACCCCCGGAAAGGTGGCAACTTGGCTGAGAGGTGGGTGGGGCT CATGGAACCGGTAGAGACCTGGACCCCCGGAATGGTGGCAACTTGGCTGAGAGGTGGGTGGGGCT A T CNKSR1 Ensembl:ENSG00000142675 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26177530..26177647 26863196 MeRIP-seq:(Medium) rs201291243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18965046 Human_Splice_Rec_33281,Human_Splice_Rec_33297,Human_Splice_Rec_33309,Human_Splice_Rec_33349,Human_Splice_Rec_33353,Human_Splice_Rec_33393,Human_Splice_Rec_33417 63917 RMVar_ID_63917 Human_SNP_ID_6971980 m1A Human chr1 + 26271106 26271106 26271106 GTCCTGGCAGAAGCGATACGATTCGCTCCAAAAGGTGACTGAGGGTGTCCAGGCTGTAACGGAGG GTCCTGGCAGAAGCGATACGATTCGCTCCAAAGGGTGACTGAGGGTGTCCAGGCTGTAACGGAGG A G CEP85 Ensembl:ENSG00000130695 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26271077..26271158 26863196 MeRIP-seq:(Medium) rs1273990139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849679,Human_RBP_ID_2140856,Human_RBP_ID_5518734,Human_RBP_ID_19034323,Human_RBP_ID_26310586 Human_Splice_Rec_33658,Human_Splice_Rec_33659,Human_Splice_Rec_33684,Human_Splice_Rec_33685,Human_Splice_Rec_33710,Human_Splice_Rec_33711,Human_Splice_Rec_33730,Human_Splice_Rec_33731,Human_Splice_Rec_33742,Human_Splice_Rec_33743,Human_Splice_Rec_33751 RMVar_hsa_circ_4270,RMVar_hsa_circ_95267,RMVar_hsa_circ_115996,RMVar_hsa_circ_130623,RMVar_hsa_circ_130627,RMVar_hsa_circ_95811,RMVar_hsa_circ_119831,RMVar_hsa_circ_130634,RMVar_hsa_circ_130635,RMVar_hsa_circ_337278,RMVar_hsa_circ_130637,RMVar_hsa_circ_71529 63918 RMVar_ID_63918 Human_SNP_ID_6974819 m1A Human chr1 + 26280736 26280736 26280736 AGCATTTCCCCCATAAATCCTCCAGCCTATCCACTAACCCCTACCCACCCTCTGTCCCCAGATCA AGCATTTCCCCCATAAATCCTCCAGCCTATCCGCTAACCCCTACCCACCCTCTGTCCCCAGATCA A G SH3BGRL3 Ensembl:ENSG00000142669 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:26280734..26280812 26863196 MeRIP-seq:(Medium) rs780559098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22633208,Human_RBP_ID_22734634 RMVar_hsa_circ_113817,RMVar_hsa_circ_130638 63919 RMVar_ID_63919 Human_SNP_ID_6975013 m1A Human chr1 - 26281168 26281168 26281168 AGGTCCTTCATGGCCAGGTGAAGGCTGGGGGGAGTGTGGTGATGGAGTCCAGCAGGGGAACTCTG AGGTCCTTCATGGCCAGGTGAAGGCTGGGGGGTGTGTGGTGATGGAGTCCAGCAGGGGAACTCTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26281119..26281318 26863196 MeRIP-seq:(Medium) rs1174516316 Functional Loss SNV dbSNP153 33..33 33 - - - 63920 RMVar_ID_63920 Human_SNP_ID_6975382 m1A Human chr1 + 26282392 26282338 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT _________________________________CCGGGACCGGGACAGGGACCAGGACTGAATTT GCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACTGGGGCCGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) rs1557677297 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_130641 63921 RMVar_ID_63921 Human_SNP_ID_6975563 m1A Human chr1 + 26282392 26282390 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT GGGCCGGGACCGGGACCGGGACTGGGGCCGG__CCGGGACCGGGACAGGGACCAGGACTGAATTT GGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) rs779402517 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_130641 63922 RMVar_ID_63922 Human_SNP_ID_6975564 m1A Human chr1 + 26282392 26282392 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT GGGCCGGGACCGGGACCGGGACTGGGGCCGGGGCCGGGACCGGGACAGGGACCAGGACTGAATTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) rs1134580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130641 63923 RMVar_ID_63923 Human_SNP_ID_6975696 m1A Human chr1 + 26282564 26282564 26282564 ATGTGCTGAAGATCTCAAAGGCAGAGGCATCCATGACCCTGGGGACCAGGCAGAGCAGATCAGGC ATGTGCTGAAGATCTCAAAGGCAGAGGCATCCCTGACCCTGGGGACCAGGCAGAGCAGATCAGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26282367..26282744 32194978 MeRIP-seq:(Medium) rs761538125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130641 63924 RMVar_ID_63924 Human_SNP_ID_6975697 m1A Human chr1 + 26282564 26282564 26282564 ATGTGCTGAAGATCTCAAAGGCAGAGGCATCCATGACCCTGGGGACCAGGCAGAGCAGATCAGGC ATGTGCTGAAGATCTCAAAGGCAGAGGCATCCGTGACCCTGGGGACCAGGCAGAGCAGATCAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26282367..26282744 32194978 MeRIP-seq:(Medium) rs761538125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130641 63925 RMVar_ID_63925 Human_SNP_ID_6976327 m1A Human chr1 - 26284467 26284467 26284467 CCCTTCTTTCTTGCCAGGTGAGTGACTTGCGCAATCAGGTCTACCTGGAGGATGGACTGGACCCC CCCTTCTTTCTTGCCAGGTGAGTGACTTGCGCTATCAGGTCTACCTGGAGGATGGACTGGACCCC T A UBXN11 Ensembl:ENSG00000158062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26284418..26284726 26863196 MeRIP-seq:(Medium) rs1204323059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851334,Human_RBP_ID_5108503,Human_RBP_ID_5335059,Human_RBP_ID_18965050,Human_RBP_ID_19037281,Human_RBP_ID_22535023,Human_RBP_ID_22871734,Human_RBP_ID_27799865 Human_Splice_Rec_33774,Human_Splice_Rec_33822,Human_Splice_Rec_33872,Human_Splice_Rec_33920,Human_Splice_Rec_33948,Human_Splice_Rec_33978 RMVar_hsa_circ_86119,RMVar_hsa_circ_20083,RMVar_hsa_circ_130642,RMVar_hsa_circ_323513 63926 RMVar_ID_63926 Human_SNP_ID_6978967 m1A Human chr1 + 26294304 26294304 26294304 TGAGTCCTCCTGGTCCATGGGCTCGCCCACCCACTGCAGGCCATAGTCACTGAGGAACCGCTGTG TGAGTCCTCCTGGTCCATGGGCTCGCCCACCCGCTGCAGGCCATAGTCACTGAGGAACCGCTGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:26294262..26294354;chr1:26294157..26294384 26863196 MeRIP-seq:(Medium) rs757340890 Functional Loss SNV dbSNP153 33..33 33 - - - 63927 RMVar_ID_63927 Human_SNP_ID_6979249 m1A Human chr1 - 26295529 26295526 26295529 GTGTGGAGGAAGGAGAAGAACGGGAAAAGAGAAGAGGTCGTGGGGGCCTTATCACATTGGAGCCG GTGTGGAGGAAGGAGAAGAACGGGAAAAGAGA___GGTCGTGGGGGCCTTATCACATTGGAGCCG CTCT C UBXN11 Ensembl:ENSG00000158062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26295527..26295686 26863196 MeRIP-seq:(Medium) rs1454549999 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_86119,RMVar_hsa_circ_38490,RMVar_hsa_circ_130642,RMVar_hsa_circ_109769,RMVar_hsa_circ_130643,RMVar_hsa_circ_130644,RMVar_hsa_circ_327102 63928 RMVar_ID_63928 Human_SNP_ID_6979919 m1A Human chr1 + 26297954 26297954 26297954 CTCAGACCGGCCCCTGGCCCTCTCCCACCTGGAGCCCCACCTTGGACAGTATCTCATCAGTCTGG CTCAGACCGGCCCCTGGCCCTCTCCCACCTGGTGCCCCACCTTGGACAGTATCTCATCAGTCTGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26297951..26298114 26863196 MeRIP-seq:(Medium) rs780080987 Functional Loss SNV dbSNP153 33..33 33 - - - 63929 RMVar_ID_63929 Human_SNP_ID_6979948 m1A Human chr1 + 26298012 26298012 26298012 AGTCTGGGCCTTCACCTGCTGCTCCAGGTCCCACAACTTCCTCGTCATGAAGGCCATCAGCTCCG AGTCTGGGCCTTCACCTGCTGCTCCAGGTCCCGCAACTTCCTCGTCATGAAGGCCATCAGCTCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:26297917..26298093 26863196 MeRIP-seq:(Medium) rs1212236662 Functional Loss SNV dbSNP153 33..33 33 - - - 63930 RMVar_ID_63930 Human_SNP_ID_7016565 m1A Human chr1 + 26432454 26432454 26432454 GGGCGGGGAGCAGCTGCGGGAGAAGCAAAGGGACGACTGAGGGAATAATCAGGAGACCACTGAGG GGGCGGGGAGCAGCTGCGGGAGAAGCAAAGGGTCGACTGAGGGAATAATCAGGAGACCACTGAGG A T DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr1:26432406..26432538;chr1:26432368..26432694 26863196 MeRIP-seq:(Medium) rs769130045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803109,Human_RBP_ID_18414899,Human_RBP_ID_22636535 Human_Splice_Rec_34487,Human_Splice_Rec_34507,Human_Splice_Rec_34521,Human_Splice_Rec_34531 RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_78540,RMVar_hsa_circ_130653,RMVar_hsa_circ_130651 63931 RMVar_ID_63931 Human_SNP_ID_7016567 m1A Human chr1 + 26432457 26432457 26432457 CGGGGAGCAGCTGCGGGAGAAGCAAAGGGACGACTGAGGGAATAATCAGGAGACCACTGAGGCGT CGGGGAGCAGCTGCGGGAGAAGCAAAGGGACGCCTGAGGGAATAATCAGGAGACCACTGAGGCGT A C DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26432381..26432691 26863196 MeRIP-seq:(Medium) rs762354313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803109,Human_RBP_ID_18414899,Human_RBP_ID_22636535 Human_Splice_Rec_34487,Human_Splice_Rec_34507,Human_Splice_Rec_34521,Human_Splice_Rec_34531 RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_78540,RMVar_hsa_circ_130653,RMVar_hsa_circ_130651 63932 RMVar_ID_63932 Human_SNP_ID_7016628 m1A Human chr1 - 26432863 26432861 26432864 GTAATCTTGGATAAACAAGAAAGAAAATAAGAAGTCACCAAGGTTTGCGAAGAGCTATAACTGAC GTAATCTTGGATAAACAAGAAAGAAAATAAG___TCACCAAGGTTTGCGAAGAGCTATAACTGAC ACTT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:26432860..26432957 26863196 MeRIP-seq:(Medium) rs1344747338 Functional Loss DEL dbSNP153 32..34 33 - - - 63933 RMVar_ID_63933 Human_SNP_ID_7016636 m1A Human chr1 - 26432897 26432897 26432897 GAAGATCACTCCAGAACAAGCAAACACCAGCCAGGTAATCTTGGATAAACAAGAAAGAAAATAAG GAAGATCACTCCAGAACAAGCAAACACCAGCCGGGTAATCTTGGATAAACAAGAAAGAAAATAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26432888..26432962 26863196 MeRIP-seq:(Medium) rs1372816091 Functional Loss SNV dbSNP153 33..33 33 - - - 63934 RMVar_ID_63934 Human_SNP_ID_7017909 m1A Human chr1 + 26438105 26438105 26438105 TCACATAGCCCAAACATATCACCTTGGGGTGTAGTGTCTTCCTTTATCCCTGAAGAATATGAGAC TCACATAGCCCAAACATATCACCTTGGGGTGTCGTGTCTTCCTTTATCCCTGAAGAATATGAGAC A C DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26438103..26438194 26863196 MeRIP-seq:(Medium) rs1440723901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4765,RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_78540,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_130651,RMVar_hsa_circ_288659 63935 RMVar_ID_63935 Human_SNP_ID_7026007 m1A Human chr1 - 26472315 26472315 26472315 GGGGGGTAGTGCGCGGAGACGGCGGCGCGCCGAGGGGGTGGGGGCGCAGTCGGGGTGGCGCGCGT GGGGGGTAGTGCGCGGAGACGGCGGCGCGCCGGGGGGGTGGGGGCGCAGTCGGGGTGGCGCGCGT T C lnc-ZNF683-3 RNACentral:URS00008BFC31 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:26472226..26472350 26863410 MeRIP-seq:(Medium) rs1306057304 Functional Loss SNV dbSNP153 33..33 33 - - - 63936 RMVar_ID_63936 Human_SNP_ID_7026130 m1A Human chr1 + 26472516 26472514 26472517 CTTTATAAACCCCCCGGAGCCCGAGCAGTGTGAAGAAGAGGCGAGAACGACCCCCGGACCGACCA CTTTATAAACCCCCCGGAGCCCGAGCAGTGT___GAAGAGGCGAGAACGACCCCCGGACCGACCA TGAA T HMGN2 Ensembl:ENSG00000198830 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs977105995 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9318722,Human_RBP_ID_9355796,Human_RBP_ID_10902021,Human_RBP_ID_18570419,Human_RBP_ID_22531926,Human_RBP_ID_26378350 63937 RMVar_ID_63937 Human_SNP_ID_7026160 m1A Human chr1 + 26472545 26472545 26472545 GTGAAGAAGAGGCGAGAACGACCCCCGGACCGACCAAAGCCCGCGCGCCGCTGCATCCCGCGTCC GTGAAGAAGAGGCGAGAACGACCCCCGGACCGGCCAAAGCCCGCGCGCCGCTGCATCCCGCGTCC A G HMGN2 Ensembl:ENSG00000198830 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:26472426..26472719 26863196 MeRIP-seq:(Medium) rs77841039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224768,Human_RBP_ID_745835,Human_RBP_ID_4093106,Human_RBP_ID_8306653,Human_RBP_ID_9318722,Human_RBP_ID_9355796,Human_RBP_ID_10902024,Human_RBP_ID_18570419,Human_RBP_ID_22531926,Human_RBP_ID_26378351,Human_RBP_ID_26860421,Human_RBP_ID_27180179,Human_RBP_ID_27396771 Human_Splice_Rec_34587,Human_Splice_Rec_34597,Human_Splice_Rec_34603,Human_Splice_Rec_34609,Human_Splice_Rec_34617,Human_Splice_Rec_34625,Human_Splice_Rec_34635,Human_Splice_Rec_34645 63938 RMVar_ID_63938 Human_SNP_ID_7026178 m1A Human chr1 + 26472585 26472572 26472585 CCGCGCGCCGCTGCATCCCGCGTCCAGCACCTACGTCCCGCTGCCGTCGCCGCCGCCACCATGCC CCGCGCGCCGCTGCATCCCG_____________CGTCCCGCTGCCGTCGCCGCCGCCACCATGCC GCGTCCAGCACCTA G HMGN2 Ensembl:ENSG00000198830 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26472526..26472650 32194978 MeRIP-seq:(Medium) rs1452198700 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_224768,Human_RBP_ID_350264,Human_RBP_ID_745835,Human_RBP_ID_1153730,Human_RBP_ID_1427601,Human_RBP_ID_1744077,Human_RBP_ID_3308293,Human_RBP_ID_4040941,Human_RBP_ID_5413835,Human_RBP_ID_5433920,Human_RBP_ID_5801786,Human_RBP_ID_8240688,Human_RBP_ID_8306653,Human_RBP_ID_8747487,Human_RBP_ID_9318723,Human_RBP_ID_9355796,Human_RBP_ID_10902024,Human_RBP_ID_17217563,Human_RBP_ID_17451993,Human_RBP_ID_17677411,Human_RBP_ID_18570419,Human_RBP_ID_22487707,Human_RBP_ID_22531926,Human_RBP_ID_22783690,Human_RBP_ID_22861146,Human_RBP_ID_24763147,Human_RBP_ID_26378351,Human_RBP_ID_26586577,Human_RBP_ID_26860421,Human_RBP_ID_27180179,Human_RBP_ID_27396771 Human_Splice_Rec_34587,Human_Splice_Rec_34597,Human_Splice_Rec_34603,Human_Splice_Rec_34609,Human_Splice_Rec_34617,Human_Splice_Rec_34625,Human_Splice_Rec_34635,Human_Splice_Rec_34645 63939 RMVar_ID_63939 Human_SNP_ID_7026182 m1A Human chr1 - 26472575 26472575 26472575 CGGCGGCGACGGCAGCGGGACGTAGGTGCTGGACGCGGGATGCAGCGGCGCGCGGGCTTTGGTCG CGGCGGCGACGGCAGCGGGACGTAGGTGCTGGTCGCGGGATGCAGCGGCGCGCGGGCTTTGGTCG T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:26472476..26473225 26863196 MeRIP-seq:(Medium) rs1141781 Functional Loss SNV dbSNP153 33..33 33 - - - 63940 RMVar_ID_63940 Human_SNP_ID_7026183 m1A Human chr1 - 26472575 26472575 26472575 CGGCGGCGACGGCAGCGGGACGTAGGTGCTGGACGCGGGATGCAGCGGCGCGCGGGCTTTGGTCG CGGCGGCGACGGCAGCGGGACGTAGGTGCTGGGCGCGGGATGCAGCGGCGCGCGGGCTTTGGTCG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:26472476..26473225 26863196 MeRIP-seq:(Medium) rs1141781 Functional Loss SNV dbSNP153 33..33 33 - - - 63941 RMVar_ID_63941 Human_SNP_ID_7026198 m1A Human chr1 - 26472594 26472594 26472594 TTTCTCTTGGGCATGGTGGCGGCGGCGACGGCAGCGGGACGTAGGTGCTGGACGCGGGATGCAGC TTTCTCTTGGGCATGGTGGCGGCGGCGACGGCGGCGGGACGTAGGTGCTGGACGCGGGATGCAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26472498..26473550 26863196 MeRIP-seq:(Medium) rs1064621 Functional Loss SNV dbSNP153 33..33 33 - - - 63942 RMVar_ID_63942 Human_SNP_ID_7026202 m1A Human chr1 - 26472599 26472599 26472599 GTACCTTTCTCTTGGGCATGGTGGCGGCGGCGACGGCAGCGGGACGTAGGTGCTGGACGCGGGAT GTACCTTTCTCTTGGGCATGGTGGCGGCGGCGGCGGCAGCGGGACGTAGGTGCTGGACGCGGGAT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control;HTR8/Svneo,Normoxia chr1:26472451..26473274;chr1:26472501..26473225;chr1:26472476..26473225;chr1:26472501..26472650;chr1:26472526..26472650 26863410,32194978 MeRIP-seq:(Medium) rs1064622 Functional Loss SNV dbSNP153 33..33 33 - - - 63943 RMVar_ID_63943 Human_SNP_ID_7026674 m1A Human chr1 + 26473479 26473479 26473479 TCAAAATCTGCAGTTTTTTGTTCTTGTTTCTTATAGGCTGAAGGGGATGCTAAGGGAGATAAAGC TCAAAATCTGCAGTTTTTTGTTCTTGTTTCTTGTAGGCTGAAGGGGATGCTAAGGGAGATAAAGC A G HMGN2 Ensembl:ENSG00000198830 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:26473476..26473550 26863196 MeRIP-seq:(Medium) rs780008190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851336,Human_RBP_ID_1744081,Human_RBP_ID_4040955,Human_RBP_ID_5332863,Human_RBP_ID_5801800,Human_RBP_ID_8306659,Human_RBP_ID_9342580,Human_RBP_ID_10902070,Human_RBP_ID_19330260,Human_RBP_ID_22535969,Human_RBP_ID_22558245,Human_RBP_ID_22783694,Human_RBP_ID_22861153,Human_RBP_ID_24555917,Human_RBP_ID_24676708,Human_RBP_ID_27180184 Human_Splice_Rec_34589,Human_Splice_Rec_34598,Human_Splice_Rec_34599,Human_Splice_Rec_34611,Human_Splice_Rec_34637,Human_Splice_Rec_34647,Human_Splice_Rec_34655 63944 RMVar_ID_63944 Human_SNP_ID_7026760 m1A Human chr1 + 26473705 26473705 26473705 TATTTCTAACTTTCTCGTTGTCTTTAATAGCCACAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG TATTTCTAACTTTCTCGTTGTCTTTAATAGCCCCAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG A C HMGN2 Ensembl:ENSG00000198830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:26473701..26473750;chr1:26473701..26473775 26863196,26863410,26863196,26863196,26863196,32194978 MeRIP-seq:(Medium) rs774791048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1427627,Human_RBP_ID_1744086,Human_RBP_ID_3308300,Human_RBP_ID_5331300,Human_RBP_ID_5801808,Human_RBP_ID_9342581,Human_RBP_ID_10902083,Human_RBP_ID_18570438,Human_RBP_ID_19034333,Human_RBP_ID_19330264,Human_RBP_ID_22430337,Human_RBP_ID_22636542,Human_RBP_ID_22861161,Human_RBP_ID_23383282,Human_RBP_ID_24555918,Human_RBP_ID_24676715,Human_RBP_ID_26860436 Human_Splice_Rec_34590,Human_Splice_Rec_34591,Human_Splice_Rec_34600,Human_Splice_Rec_34601,Human_Splice_Rec_34612,Human_Splice_Rec_34619,Human_Splice_Rec_34628,Human_Splice_Rec_34629,Human_Splice_Rec_34638,Human_Splice_Rec_34639,Human_Splice_Rec_34648,Human_Splice_Rec_34656,Human_Splice_Rec_34657 RMVar_hsa_circ_35640 63945 RMVar_ID_63945 Human_SNP_ID_7026761 m1A Human chr1 + 26473705 26473705 26473705 TATTTCTAACTTTCTCGTTGTCTTTAATAGCCACAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG TATTTCTAACTTTCTCGTTGTCTTTAATAGCCGCAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG A G HMGN2 Ensembl:ENSG00000198830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:26473701..26473750;chr1:26473701..26473775 26863196,26863410,26863196,26863196,26863196,32194978 MeRIP-seq:(Medium) rs774791048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1427627,Human_RBP_ID_1744086,Human_RBP_ID_3308300,Human_RBP_ID_5331300,Human_RBP_ID_5801808,Human_RBP_ID_9342581,Human_RBP_ID_10902083,Human_RBP_ID_18570438,Human_RBP_ID_19034333,Human_RBP_ID_19330264,Human_RBP_ID_22430337,Human_RBP_ID_22636542,Human_RBP_ID_22861161,Human_RBP_ID_23383282,Human_RBP_ID_24555918,Human_RBP_ID_24676715,Human_RBP_ID_26860436 Human_Splice_Rec_34590,Human_Splice_Rec_34591,Human_Splice_Rec_34600,Human_Splice_Rec_34601,Human_Splice_Rec_34612,Human_Splice_Rec_34619,Human_Splice_Rec_34628,Human_Splice_Rec_34629,Human_Splice_Rec_34638,Human_Splice_Rec_34639,Human_Splice_Rec_34648,Human_Splice_Rec_34656,Human_Splice_Rec_34657 RMVar_hsa_circ_35640 63946 RMVar_ID_63946 Human_SNP_ID_7026762 m1A Human chr1 + 26473705 26473705 26473705 TATTTCTAACTTTCTCGTTGTCTTTAATAGCCACAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG TATTTCTAACTTTCTCGTTGTCTTTAATAGCCTCAGAGAAGATCCGCGAGGTTGTCTGCTGTAAG A T HMGN2 Ensembl:ENSG00000198830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:26473701..26473750;chr1:26473701..26473775 26863196,26863410,26863196,26863196,26863196,32194978 MeRIP-seq:(Medium) rs774791048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1427627,Human_RBP_ID_1744086,Human_RBP_ID_3308300,Human_RBP_ID_5331300,Human_RBP_ID_5801808,Human_RBP_ID_9342581,Human_RBP_ID_10902083,Human_RBP_ID_18570438,Human_RBP_ID_19034333,Human_RBP_ID_19330264,Human_RBP_ID_22430337,Human_RBP_ID_22636542,Human_RBP_ID_22861161,Human_RBP_ID_23383282,Human_RBP_ID_24555918,Human_RBP_ID_24676715,Human_RBP_ID_26860436 Human_Splice_Rec_34590,Human_Splice_Rec_34591,Human_Splice_Rec_34600,Human_Splice_Rec_34601,Human_Splice_Rec_34612,Human_Splice_Rec_34619,Human_Splice_Rec_34628,Human_Splice_Rec_34629,Human_Splice_Rec_34638,Human_Splice_Rec_34639,Human_Splice_Rec_34648,Human_Splice_Rec_34656,Human_Splice_Rec_34657 RMVar_hsa_circ_35640 63947 RMVar_ID_63947 Human_SNP_ID_7027311 m1A Human chr1 - 26475272 26475272 26475272 AAAACAACAATGAAGTGTTCTGTGTGCTAACAACATAGCTTTTAAAAAAAAAAAAAAAGTAAAAC AAAACAACAATGAAGTGTTCTGTGTGCTAACAGCATAGCTTTTAAAAAAAAAAAAAAAGTAAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26475251..26475325 26863196 MeRIP-seq:(Medium) rs1246202604 Functional Loss SNV dbSNP153 33..33 33 - - - 63948 RMVar_ID_63948 Human_SNP_ID_7042501 m1A Human chr1 - 26529816 26529816 26529816 GGCTCTGCGACCCGAACCGCCGCGCCCCCCCGAGCCCCTCGCGCTCCGGCTGGGCCGTCCGCCGC GGCTCTGCGACCCGAACCGCCGCGCCCCCCCGGGCCCCTCGCGCTCCGGCTGGGCCGTCCGCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26529772..26530030 26863196 MeRIP-seq:(Medium) rs977268236 Functional Loss SNV dbSNP153 33..33 33 - - - 63949 RMVar_ID_63949 Human_SNP_ID_7042578 m1A Human chr1 - 26529964 26529964 26529964 CCCGCTCACTCACCTCCGGGTCCAGAGGCACTAGCTCCATGAGCGGCCAGGGCTCCTTGAGCTGG CCCGCTCACTCACCTCCGGGTCCAGAGGCACTGGCTCCATGAGCGGCCAGGGCTCCTTGAGCTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26529775..26530771 26863196 MeRIP-seq:(Medium) rs1358727405 Functional Loss SNV dbSNP153 33..33 33 - - - 63950 RMVar_ID_63950 Human_SNP_ID_7042579 m1A Human chr1 - 26529967 26529967 26529967 CGCCCCGCTCACTCACCTCCGGGTCCAGAGGCACTAGCTCCATGAGCGGCCAGGGCTCCTTGAGC CGCCCCGCTCACTCACCTCCGGGTCCAGAGGCGCTAGCTCCATGAGCGGCCAGGGCTCCTTGAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26529917..26530024 32194978 MeRIP-seq:(Medium) rs1419287386 Functional Loss SNV dbSNP153 33..33 33 - - - 63951 RMVar_ID_63951 Human_SNP_ID_7044201 m1A Human chr1 - 26536853 26536853 26536853 CTTACACGCTTGGGAGAAAGACTCTGTGGGGCACCCCCACCCTTAGGTGCTCCCAATAGCCATGG CTTACACGCTTGGGAGAAAGACTCTGTGGGGCCCCCCCACCCTTAGGTGCTCCCAATAGCCATGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26536848..26537033 26863196 MeRIP-seq:(Medium) rs1048594664 Functional Loss SNV dbSNP153 33..33 33 - - - 63952 RMVar_ID_63952 Human_SNP_ID_7046519 m1A Human chr1 + 26546827 26546827 26546827 GGACTTGGGCAGGGGAGCCTCCTGCTGCCTGGATGGGGCCCACCATGCCCACCAGCTCTGTCCCT GGACTTGGGCAGGGGAGCCTCCTGCTGCCTGGCTGGGGCCCACCATGCCCACCAGCTCTGTCCCT A C RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26546825..26546950 26863196 MeRIP-seq:(Medium) rs774042153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22535027,Human_RBP_ID_22633218 RMVar_hsa_circ_9625,RMVar_hsa_circ_130668 63953 RMVar_ID_63953 Human_SNP_ID_7046520 m1A Human chr1 + 26546827 26546827 26546827 GGACTTGGGCAGGGGAGCCTCCTGCTGCCTGGATGGGGCCCACCATGCCCACCAGCTCTGTCCCT GGACTTGGGCAGGGGAGCCTCCTGCTGCCTGGGTGGGGCCCACCATGCCCACCAGCTCTGTCCCT A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26546825..26546950 26863196 MeRIP-seq:(Medium) rs774042153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22535027,Human_RBP_ID_22633218 RMVar_hsa_circ_9625,RMVar_hsa_circ_130668 63954 RMVar_ID_63954 Human_SNP_ID_7083806 m1A Human chr1 - 26695526 26695526 26695526 CCGCCGAAGGCTTCGGAGAAAACCCGGCCCGGAGCCCGCGCATCTCTGGAGCCTGCGCCGCCTCC CCGCCGAAGGCTTCGGAGAAAACCCGGCCCGGGGCCCGCGCATCTCTGGAGCCTGCGCCGCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26695481..26695555 26863196 MeRIP-seq:(Medium) rs935213691 Functional Loss SNV dbSNP153 33..33 33 - - - 63955 RMVar_ID_63955 Human_SNP_ID_7083905 m1A Human chr1 - 26695767 26695767 26695767 CGGTCGGCCGGACTGAGCGGCTAGAGCGCCCCACTCTCCTCCGAGTCCCCCTCACTCCGACACGA CGGTCGGCCGGACTGAGCGGCTAGAGCGCCCCTCTCTCCTCCGAGTCCCCCTCACTCCGACACGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:26695668..26695884;chr1:26695718..26695811 26863196 MeRIP-seq:(Medium) rs1179278134 Functional Loss SNV dbSNP153 33..33 33 - - - 63956 RMVar_ID_63956 Human_SNP_ID_7084149 m1A Human chr1 + 26696272 26696272 26696272 GGCGGGGGGGAGAGGAGCGAGCGCAGCGCAGCAGCGGAGCCCCGCGAGGCCCGCCCGGGCGGGTG GGCGGGGGGGAGAGGAGCGAGCGCAGCGCAGCGGCGGAGCCCCGCGAGGCCCGCCCGGGCGGGTG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:26696123..26696293 26863196 MeRIP-seq:(Medium) rs1468673661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 63957 RMVar_ID_63957 Human_SNP_ID_7084294 m1A Human chr1 + 26696532 26696526 26696532 GAGGAGGCGGGGGGCGAGGCGGCGGCGGCGGCAGCGGCCGAGCGCGGGGAAATGAAGGCAGCCGC GAGGAGGCGGGGGGCGAGGCGGCGGCG______GCGGCCGAGCGCGGGGAAATGAAGGCAGCCGC GGCGGCA G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26696451..26696550 26863196 MeRIP-seq:(Medium) rs1553145848 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_3933092,Human_RBP_ID_4072628,Human_RBP_ID_5137434,Human_RBP_ID_5234283,Human_RBP_ID_5337354,Human_RBP_ID_9318736,Human_RBP_ID_9411024,Human_RBP_ID_18455067,Human_RBP_ID_18473835,Human_RBP_ID_22707709,Human_RBP_ID_24528683,Human_RBP_ID_26773008 RMVar_hsa_circ_268846 63958 RMVar_ID_63958 Human_SNP_ID_7084299 m1A Human chr1 + 26696532 26696532 26696532 GAGGAGGCGGGGGGCGAGGCGGCGGCGGCGGCAGCGGCCGAGCGCGGGGAAATGAAGGCAGCCGC GAGGAGGCGGGGGGCGAGGCGGCGGCGGCGGCGGCGGCCGAGCGCGGGGAAATGAAGGCAGCCGC A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26696451..26696550 26863196 MeRIP-seq:(Medium) rs1158398856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3933092,Human_RBP_ID_4072628,Human_RBP_ID_5137434,Human_RBP_ID_5234283,Human_RBP_ID_5337354,Human_RBP_ID_9318736,Human_RBP_ID_9411024,Human_RBP_ID_18455067,Human_RBP_ID_18473835,Human_RBP_ID_22707709,Human_RBP_ID_24528683,Human_RBP_ID_26773008 RMVar_hsa_circ_268846 63959 RMVar_ID_63959 Human_SNP_ID_7084306 m1A Human chr1 + 26696549 26696549 26696549 GGCGGCGGCGGCGGCAGCGGCCGAGCGCGGGGAAATGAAGGCAGCCGCCGGGCAGGAAAGCGAGG GGCGGCGGCGGCGGCAGCGGCCGAGCGCGGGGGAATGAAGGCAGCCGCCGGGCAGGAAAGCGAGG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:26696351..26696752;chr1:26696351..26697541 26863196 MeRIP-seq:(Medium) rs1016806450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3933092,Human_RBP_ID_5137434,Human_RBP_ID_18455068,Human_RBP_ID_22369284,Human_RBP_ID_22707709,Human_RBP_ID_24528683 RMVar_hsa_circ_268846 63960 RMVar_ID_63960 Human_SNP_ID_7084318 m1A Human chr1 + 26696570 26696570 26696570 CGAGCGCGGGGAAATGAAGGCAGCCGCCGGGCAGGAAAGCGAGGGCCCCGCCGTGGGGCCGCCGC CGAGCGCGGGGAAATGAAGGCAGCCGCCGGGCTGGAAAGCGAGGGCCCCGCCGTGGGGCCGCCGC A T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26696427..26696624 26863196 MeRIP-seq:(Medium) rs1034809221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190911,Human_RBP_ID_3933092,Human_RBP_ID_8167781,Human_RBP_ID_18455068,Human_RBP_ID_22369284,Human_RBP_ID_22707044,Human_RBP_ID_26773009 RMVar_hsa_circ_268846 63961 RMVar_ID_63961 Human_SNP_ID_7084619 m1A Human chr1 + 26697047 26697047 26697047 CCACGGCTTCCCCAACCACCAGTACAACTCCTACTACCCCAACCGCAGCGCCTACCCCCCGCCCG CCACGGCTTCCCCAACCACCAGTACAACTCCTGCTACCCCAACCGCAGCGCCTACCCCCCGCCCG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:26696975..26697200;chr1:26696811..26697539;chr1:26696803..26697470 26863196 MeRIP-seq:(Medium) rs763817285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_977168,Human_RBP_ID_9318740,Human_RBP_ID_18928126,Human_RBP_ID_27396794 RMVar_hsa_circ_268846 63962 RMVar_ID_63962 Human_SNP_ID_7084816 m1A Human chr1 + 26697365 26697365 26697365 CTACCCCGGGGGCGACTACAGTGGCGGGCCCCAGGACGGGGGCGCCGGCAAGGGCCCGGCGGACA CTACCCCGGGGGCGACTACAGTGGCGGGCCCCCGGACGGGGGCGCCGGCAAGGGCCCGGCGGACA A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26697251..26697475 26863196 MeRIP-seq:(Medium) rs992667636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330125,Human_RBP_ID_5136145 RMVar_hsa_circ_268846 63963 RMVar_ID_63963 Human_SNP_ID_7093634 m1A Human chr1 + 26729767 26729767 26729767 CCGTCAGGACCGCAGCAAGGACATGGGTACCCAGGGCAGCCATACGGGTCCCAGACCCCGCAGCG CCGTCAGGACCGCAGCAAGGACATGGGTACCCCGGGCAGCCATACGGGTCCCAGACCCCGCAGCG A C ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26729651..26729904 26863196 MeRIP-seq:(Medium) rs781202939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10905002,Human_RBP_ID_17222325 Human_Splice_Rec_35039,Human_Splice_Rec_35077,Human_Splice_Rec_35113,Human_Splice_Rec_35117,Human_Splice_Rec_35155,Human_Splice_Rec_35157,Human_Splice_Rec_35193,Human_Splice_Rec_35225 Human_miRNA_ID_1934291,Human_miRNA_ID_3089535,Human_miRNA_ID_3126335,Human_miRNA_ID_3126487 RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_268846,RMVar_hsa_circ_272963,RMVar_hsa_circ_114027,RMVar_hsa_circ_130681,RMVar_hsa_circ_95019,RMVar_hsa_circ_130682,RMVar_hsa_circ_130680 63964 RMVar_ID_63964 Human_SNP_ID_7094069 m1A Human chr1 - 26731416 26731413 26731416 GGGCTGGCTCTGGGGGTGCTGCTGTGTCGTCGACTGCTGGGAGGGGTATGGAGCCGGGGACTGCT GGGCTGGCTCTGGGGGTGCTGCTGTGTCGTCGGGGTCTGGGAGGGGTATGGAGCCGGGGACTGCT CAGT ACCC - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:26731232..26731550 26863196 MeRIP-seq:(Medium) rs1557592309 Functional Loss MNV dbSNP153 33..36 33 - - - 63965 RMVar_ID_63965 Human_SNP_ID_7102365 m1A Human chr1 + 26763221 26763221 26763221 TTGGGTCAGGGATGTGTCCCCCACCAGGGGGCATGAACCGGAAAACCCAAGAAACTGCTGTCGCC TTGGGTCAGGGATGTGTCCCCCACCAGGGGGCGTGAACCGGAAAACCCAAGAAACTGCTGTCGCC A G ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26760979..26763247 32194978 MeRIP-seq:(Medium) rs140664170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_35051,Human_Splice_Rec_35089,Human_Splice_Rec_35129,Human_Splice_Rec_35169,Human_Splice_Rec_35205,Human_Splice_Rec_35237,Human_Splice_Rec_35269 RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_268846,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_99495,RMVar_hsa_circ_130684,RMVar_hsa_circ_61331,RMVar_hsa_circ_279158,RMVar_hsa_circ_100919,RMVar_hsa_circ_25221,RMVar_hsa_circ_130686,RMVar_hsa_circ_130687,RMVar_hsa_circ_50375 63966 RMVar_ID_63966 Human_SNP_ID_7104415 m1A Human chr1 - 26771296 26771296 26771296 ACCAGGAGAGGGAGGCTGGATCTTGGGCTGGGACTTCTTGGAATCAGCAGCTGCAAAGATGTCTG ACCAGGAGAGGGAGGCTGGATCTTGGGCTGGGTCTTCTTGGAATCAGCAGCTGCAAAGATGTCTG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26771246..26771347 32194978 MeRIP-seq:(Medium) rs777420181 Functional Loss SNV dbSNP153 33..33 33 - - - 63967 RMVar_ID_63967 Human_SNP_ID_7105127 m1A Human chr1 - 26773733 26773733 26773733 AGTGGCGAAGCCTGATCCATAGCAGCACCGAGACCAGGCTTTACTCACCGTTGCTGCTGCTGCTG AGTGGCGAAGCCTGATCCATAGCAGCACCGAGCCCAGGCTTTACTCACCGTTGCTGCTGCTGCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26773731..26773821 26863196 MeRIP-seq:(Medium) rs2273016 Functional Loss SNV dbSNP153 33..33 33 - - - 63968 RMVar_ID_63968 Human_SNP_ID_7105510 m1A Human chr1 + 26774963 26774963 26774963 TCCATCTAACTACCAGCCCCCACCAAGCATGCAGAATCACATTCCTCAGGTATCCAGCCCTGCTC TCCATCTAACTACCAGCCCCCACCAAGCATGCGGAATCACATTCCTCAGGTATCCAGCCCTGCTC A G ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:26774855..26775074 26863196 MeRIP-seq:(Medium) rs763065019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17338855 Human_miRNA_ID_1932657,Human_miRNA_ID_2196465,Human_miRNA_ID_2935477 RMVar_hsa_circ_266788,RMVar_hsa_circ_25221,RMVar_hsa_circ_130689,RMVar_hsa_circ_372171,RMVar_hsa_circ_322540,RMVar_hsa_circ_43796 63969 RMVar_ID_63969 Human_SNP_ID_7105543 m1A Human chr1 - 26775054 26775054 26775054 ACTGGGGGACCTGCCTTCTGCATTTTCATCCCAGAGTGCAGGAATGGAGACTTGCTAGGAGAGGT ACTGGGGGACCTGCCTTCTGCATTTTCATCCCGGAGTGCAGGAATGGAGACTTGCTAGGAGAGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26775004..26775155 32194978 MeRIP-seq:(Medium) rs1467938030 Functional Loss SNV dbSNP153 33..33 33 - - - 63970 RMVar_ID_63970 Human_SNP_ID_7106749 m1A Human chr1 + 26779198 26779198 26779198 AGCTCCCATGGAGGGTGGGGAAGAAGAAGAAGAACTTCTAGGTCCTAAACTAGAAGAGGAAGAAG AGCTCCCATGGAGGGTGGGGAAGAAGAAGAAGTACTTCTAGGTCCTAAACTAGAAGAGGAAGAAG A T ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26779148..26779299 26863196 MeRIP-seq:(Medium) rs1309206594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24595,Human_RBP_ID_190186,Human_RBP_ID_849699,Human_RBP_ID_3935592,Human_RBP_ID_5159220,Human_RBP_ID_5518737,Human_RBP_ID_5802698,Human_RBP_ID_8747574,Human_RBP_ID_9342016,Human_RBP_ID_17646306,Human_RBP_ID_18187616,Human_RBP_ID_18410099,Human_RBP_ID_22026295,Human_RBP_ID_22870784,Human_RBP_ID_24541439,Human_RBP_ID_26310606,Human_RBP_ID_27799875 RMVar_hsa_circ_266788,RMVar_hsa_circ_130692 63971 RMVar_ID_63971 Human_SNP_ID_7121230 m1A Human chr1 + 26833257 26833257 26833257 ATATCAGACAGAGAAGAAAGGAGGGAAGGAGGATGAAGGCTACAGGGAGGGTGTGTGATTTTACA ATATCAGACAGAGAAGAAAGGAGGGAAGGAGGGTGAAGGCTACAGGGAGGGTGTGTGATTTTACA A G ZDHHC18 Ensembl:ENSG00000204160 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26833250..26833492 26863196 MeRIP-seq:(Medium) rs1557640487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75662,RMVar_hsa_circ_130695 63972 RMVar_ID_63972 Human_SNP_ID_7126839 m1A Human chr1 + 26855359 26855359 26855359 CAAGTGAAGGTTGGCCTGAGTCTGGGCCGGAAACTCAGAGGATGTTTCTCCTCTGCTGGGAGCTG CAAGTGAAGGTTGGCCTGAGTCTGGGCCGGAACCTCAGAGGATGTTTCTCCTCTGCTGGGAGCTG A C ZDHHC18 Ensembl:ENSG00000204160 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26854958..26855458 32194978 MeRIP-seq:(Medium) rs1417370893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350372,Human_RBP_ID_1744232 Human_miRNA_ID_2368711,Human_miRNA_ID_2730460 RMVar_hsa_circ_75662,RMVar_hsa_circ_130695,RMVar_hsa_circ_126073,RMVar_hsa_circ_130697,RMVar_hsa_circ_109464,RMVar_hsa_circ_130698 63973 RMVar_ID_63973 Human_SNP_ID_7126898 m1A Human chr1 - 26855608 26855608 26855608 TCTAGCCAGCTTCTTCCTCACCTCCCAGGGCCACTGCAGTGATGGCCCAGGGCCCTGAGGCTGGG TCTAGCCAGCTTCTTCCTCACCTCCCAGGGCCTCTGCAGTGATGGCCCAGGGCCCTGAGGCTGGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26855557..26855657 32194978 MeRIP-seq:(Medium) rs1557647545 Functional Loss SNV dbSNP153 33..33 33 - - - 63974 RMVar_ID_63974 Human_SNP_ID_7128676 m1A Human chr1 - 26863321 26863319 26863322 GGCTACTGAGAGCAGGTTTCGCTCTTCGCAGGAGAGCTCCTCGCCCTTCTCCACGGCGCCTTTCA GGCTACTGAGAGCAGGTTTCGCTCTTCGCAG___AGCTCCTCGCCCTTCTCCACGGCGCCTTTCA TCTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26863151..26863536 26863196 MeRIP-seq:(Medium) rs1314504941 Functional Loss DEL dbSNP153 32..34 33 - - - 63975 RMVar_ID_63975 Human_SNP_ID_7128694 m1A Human chr1 - 26863364 26863364 26863364 GCACCCTCCAGGCAGCCCTCTGGCCGCCCACCACGTTCTTATAGGCTACTGAGAGCAGGTTTCGC GCACCCTCCAGGCAGCCCTCTGGCCGCCCACCTCGTTCTTATAGGCTACTGAGAGCAGGTTTCGC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26863201..26863450 26863196 MeRIP-seq:(Medium) rs1470145884 Functional Loss SNV dbSNP153 33..33 33 - - - 63976 RMVar_ID_63976 Human_SNP_ID_7128705 m1A Human chr1 + 26863402 26863402 26863402 GCGGCCAGAGGGCTGCCTGGAGGGTGCTGTCCAGTATTGAGCAGAAAAGCAACGAGGAGGGCTCG GCGGCCAGAGGGCTGCCTGGAGGGTGCTGTCCGGTATTGAGCAGAAAAGCAACGAGGAGGGCTCG A G SFN Ensembl:ENSG00000175793 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:26863101..26864475;chr1:26863126..26864025 26863196 MeRIP-seq:(Medium) rs1469586278 Functional Loss SNV dbSNP153 33..33 33 - - - 63977 RMVar_ID_63977 Human_SNP_ID_7128845 m1A Human chr1 - 26863745 26863745 26863745 CCTCGGGGCTGTTGGCGATCTCGTAGTGGAAGACGGAAAAGTTCAGGGCCAGGCCCAGGCGGATG CCTCGGGGCTGTTGGCGATCTCGTAGTGGAAGCCGGAAAAGTTCAGGGCCAGGCCCAGGCGGATG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:26863651..26863875 26863196 MeRIP-seq:(Medium) rs775634605 Functional Loss SNV dbSNP153 33..33 33 - - - 63978 RMVar_ID_63978 Human_SNP_ID_7128980 m1A Human chr1 - 26864101 26864101 26864101 GAAGAGTGGGATCCCCAGCCCCAGGTGGCCTCAGCTCTGCCAGTCCCTCTCCACGGAGCCCTTTG GAAGAGTGGGATCCCCAGCCCCAGGTGGCCTCGGCTCTGCCAGTCCCTCTCCACGGAGCCCTTTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:26863989..26864150 26863196 MeRIP-seq:(Medium) rs1330650090 Functional Loss SNV dbSNP153 33..33 33 - - - 63979 RMVar_ID_63979 Human_SNP_ID_7129003 m1A Human chr1 + 26864212 26864212 26864212 GCTCTCCGCACCCGCTTCCTCCCGACCCCAGGACCAGGCTACTTCTCCCCTCCTCTTGCCTCCCT GCTCTCCGCACCCGCTTCCTCCCGACCCCAGGTCCAGGCTACTTCTCCCCTCCTCTTGCCTCCCT A T SFN Ensembl:ENSG00000175793 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:26863951..26864290 26863196 MeRIP-seq:(Medium) rs1406900592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17647436,Human_RBP_ID_27396915 63980 RMVar_ID_63980 Human_SNP_ID_7132365 m1A Human chr1 - 26876298 26876298 26876298 GGCAGGAGAATCGCTTGAACCTGGGAGGCGGAAGTTTCAGTGAGCGGAGATCGCGCCATTGCACT GGCAGGAGAATCGCTTGAACCTGGGAGGCGGACGTTTCAGTGAGCGGAGATCGCGCCATTGCACT T G GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1176307725 Functional Loss SNV dbSNP153 33..33 33 - - - 63981 RMVar_ID_63981 Human_SNP_ID_7133954 m1A Human chr1 + 26883146 26883146 26883146 TTTCCACAATTGCAGGGGCTTTTCTAAAATGTACATCTGATTGTGTCACACCCTGTTCAACAGTA TTTCCACAATTGCAGGGGCTTTTCTAAAATGTGCATCTGATTGTGTCACACCCTGTTCAACAGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26883095..26883344 26863196 MeRIP-seq:(Medium) rs1557655347 Functional Loss SNV dbSNP153 33..33 33 - - - 63982 RMVar_ID_63982 Human_SNP_ID_7133981 m1A Human chr1 - 26883293 26883293 26883293 GGAGTCCAGTTCCTGGTGTGTTGCATGTGAAGAGGAAAGGGCGTTGCAGGGGTACAGGCAGGGCT GGAGTCCAGTTCCTGGTGTGTTGCATGTGAAGTGGAAAGGGCGTTGCAGGGGTACAGGCAGGGCT T A GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26882902..26883347 26863196 MeRIP-seq:(Medium) rs1289255436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21962863,Human_RBP_ID_23383665 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 63983 RMVar_ID_63983 Human_SNP_ID_7135828 m1A Human chr1 - 26889783 26889783 26889783 GCTGCGTGCCAAGCTCGACCCCCTCCGCGGCCACTACTTCCTCTTCGACTGCCCAGGCCAGGTGG GCTGCGTGCCAAGCTCGACCCCCTCCGCGGCCTCTACTTCCTCTTCGACTGCCCAGGCCAGGTGG T A GPN2 Ensembl:ENSG00000142751 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26889733..26889862 26863196 MeRIP-seq:(Medium) rs778495588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_35411,Human_Splice_Rec_35429 RMVar_hsa_circ_98240,RMVar_hsa_circ_130702 63984 RMVar_ID_63984 Human_SNP_ID_7135869 m1A Human chr1 - 26889849 26889849 26889849 GCTGCGCCTGGGGCCCAACGGCGGCCTGCTCTACTGCATGGAGTACCTGGAAGCCAACCTGGACT GCTGCGCCTGGGGCCCAACGGCGGCCTGCTCTGCTGCATGGAGTACCTGGAAGCCAACCTGGACT T C GPN2 Ensembl:ENSG00000142751 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26889798..26890247 32194978 MeRIP-seq:(Medium) rs753625668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22023023 RMVar_hsa_circ_98240,RMVar_hsa_circ_130702 63985 RMVar_ID_63985 Human_SNP_ID_7135945 m1A Human chr1 - 26890023 26890023 26890023 GATCGGCCCGCCGGGCTCAGGGAAGACCACGTACTGCCTGGGCATGAGTGAGTTCCTGCGCGCGC GATCGGCCCGCCGGGCTCAGGGAAGACCACGTCCTGCCTGGGCATGAGTGAGTTCCTGCGCGCGC T G GPN2 Ensembl:ENSG00000142751 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26890015..26890201 26863196 MeRIP-seq:(Medium) rs1235711946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073737,Human_RBP_ID_5803019,Human_RBP_ID_22429162,Human_RBP_ID_23383669 RMVar_hsa_circ_98240,RMVar_hsa_circ_130702 63986 RMVar_ID_63986 Human_SNP_ID_7136968 m1A Human chr1 + 26892763 26892762 26892764 TCTCGGAGTCTCTGTTCCAGACGCATTTGGACAGAGTCTCGGGCATCCTTGTCTCCACCATCTGA TCTCGGAGTCTCTGTTCCAGACGCATTTGGAC__AGTCTCGGGCATCCTTGTCTCCACCATCTGA CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26892713..26892836 26863196 MeRIP-seq:(Medium) rs757069838 Functional Loss DEL dbSNP153 33..34 33 - - - 63987 RMVar_ID_63987 Human_SNP_ID_7139130 m1A Human chr1 - 26900407 26900406 26900408 GCGGTGCCCGGCGAGGCGGAGGAGGAGGCGACAGTTTACCTGGTAGTGAGCGGTATCCCCTCCGT GCGGTGCCCGGCGAGGCGGAGGAGGAGGCGA__GTTTACCTGGTAGTGAGCGGTATCCCCTCCGT CTG C GPATCH3 Ensembl:ENSG00000198746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26900177..26900423 26863196 MeRIP-seq:(Medium) rs1430554980 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23383672 63988 RMVar_ID_63988 Human_SNP_ID_7139132 m1A Human chr1 - 26900407 26900407 26900407 GCGGTGCCCGGCGAGGCGGAGGAGGAGGCGACAGTTTACCTGGTAGTGAGCGGTATCCCCTCCGT GCGGTGCCCGGCGAGGCGGAGGAGGAGGCGACGGTTTACCTGGTAGTGAGCGGTATCCCCTCCGT T C GPATCH3 Ensembl:ENSG00000198746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26900177..26900423 26863196 MeRIP-seq:(Medium) rs1040080036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23383672 63989 RMVar_ID_63989 Human_SNP_ID_7144610 m1A Human chr1 + 26921885 26921885 26921885 GCGGAGAGCAGGAGGAGGAGCGGTTCGACGGCATGTTGCTGGCCATGGCTCAGCAGCACGAGGGC GCGGAGAGCAGGAGGAGGAGCGGTTCGACGGCCTGTTGCTGGCCATGGCTCAGCAGCACGAGGGC A C NUDC Ensembl:ENSG00000090273 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:26921751..26921975 26863410 MeRIP-seq:(Medium) rs766575875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741750,Human_RBP_ID_4041509,Human_RBP_ID_5803030,Human_RBP_ID_9318747,Human_RBP_ID_9355810,Human_RBP_ID_26310611,Human_RBP_ID_26860641,Human_RBP_ID_27797637,Human_RBP_ID_27835120 Human_Splice_Rec_35469 RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707 63990 RMVar_ID_63990 Human_SNP_ID_7144611 m1A Human chr1 - 26921886 26921886 26921886 CGCCCTCGTGCTGCTGAGCCATGGCCAGCAACATGCCGTCGAACCGCTCCTCCTCCTGCTCTCCG CGCCCTCGTGCTGCTGAGCCATGGCCAGCAACGTGCCGTCGAACCGCTCCTCCTCCTGCTCTCCG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:26921751..26921950 26863196 MeRIP-seq:(Medium) rs1437444864 Functional Loss SNV dbSNP153 33..33 33 - - - 63991 RMVar_ID_63991 Human_SNP_ID_7150357 m1A Human chr1 + 26942683 26942683 26942683 TGTAAGCAGGATACTGAGGAAGATGAGGAGGAAGATGAGAAGGACAAAGGAAAACTGAAGCCCAA TGTAAGCAGGATACTGAGGAAGATGAGGAGGAGGATGAGAAGGACAAAGGAAAACTGAAGCCCAA A G NUDC Ensembl:ENSG00000090273 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26942651..26942725 26863196 MeRIP-seq:(Medium) rs1305680768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350405,Human_RBP_ID_860103,Human_RBP_ID_1428030,Human_RBP_ID_1744252,Human_RBP_ID_2141020,Human_RBP_ID_5803100,Human_RBP_ID_8747643,Human_RBP_ID_9319833,Human_RBP_ID_9355819,Human_RBP_ID_18524697,Human_RBP_ID_19442435,Human_RBP_ID_23383710,Human_RBP_ID_24541043,Human_RBP_ID_26309684,Human_RBP_ID_27797640 Human_Splice_Rec_35468,Human_Splice_Rec_35476,Human_Splice_Rec_35477,Human_Splice_Rec_35492 Human_miRNA_ID_2253813 RMVar_hsa_circ_91566,RMVar_hsa_circ_78830,RMVar_hsa_circ_130706,RMVar_hsa_circ_79261,RMVar_hsa_circ_125277,RMVar_hsa_circ_73686,RMVar_hsa_circ_130708,RMVar_hsa_circ_82233,RMVar_hsa_circ_130710,RMVar_hsa_circ_130712,RMVar_hsa_circ_82007,RMVar_hsa_circ_130711,RMVar_hsa_circ_269870,RMVar_hsa_circ_130713,RMVar_hsa_circ_130714 63992 RMVar_ID_63992 Human_SNP_ID_7150493 m1A Human chr1 - 26943007 26943007 26943007 TGCCGTCCTCAATGAGCCACGAGCTCTCCTCCACCTTCACTTCATTGTAGAGCTCCCCATCAATG TGCCGTCCTCAATGAGCCACGAGCTCTCCTCCGCCTTCACTTCATTGTAGAGCTCCCCATCAATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:26942618..26945139;chr1:26942623..26943110;chr1:26942759..26943116 26863196 MeRIP-seq:(Medium) rs1031525845 Functional Loss SNV dbSNP153 33..33 33 - - - 63993 RMVar_ID_63993 Human_SNP_ID_7151138 m1A Human chr1 + 26945496 26945496 26945496 GAATTCCAAGGTGAGCCCTGGCTGGTTGGGGGAGCTTCAGCAGGAAGGTGAGGGGCCTCGTTGTT GAATTCCAAGGTGAGCCCTGGCTGGTTGGGGGTGCTTCAGCAGGAAGGTGAGGGGCCTCGTTGTT A T NUDC Ensembl:ENSG00000090273 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26945494..26945596 26863196 MeRIP-seq:(Medium) rs1386749843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_977231,Human_RBP_ID_19037333 RMVar_hsa_circ_91566,RMVar_hsa_circ_78830,RMVar_hsa_circ_130706,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708,RMVar_hsa_circ_82233,RMVar_hsa_circ_130710,RMVar_hsa_circ_130712,RMVar_hsa_circ_82007,RMVar_hsa_circ_118916,RMVar_hsa_circ_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715,RMVar_hsa_circ_130716 63994 RMVar_ID_63994 Human_SNP_ID_7163011 m1A Human chr1 - 26993774 26993774 26993774 CTGATGCGGCAGCCCGGCATCCCCCGCCCCCCACCGGCGGTCTGCGGCTGTAGGTGCGCAGGGAG CTGATGCGGCAGCCCGGCATCCCCCGCCCCCCCCCGGCGGTCTGCGGCTGTAGGTGCGCAGGGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26993732..26994178 26863196 MeRIP-seq:(Medium) rs1351610767 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 63995 RMVar_ID_63995 Human_SNP_ID_7163039 m1A Human chr1 + 26993842 26993842 26993842 CTGCGGCCCGGGGGCCCAGGAGGGGACGGCAGAGCAGAGGTCGCCGCCGCCGCCCTGGGATCCCA CTGCGGCCCGGGGGCCCAGGAGGGGACGGCAGGGCAGAGGTCGCCGCCGCCGCCCTGGGATCCCA A G TRNP1 Ensembl:ENSG00000253368 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:26993726..26993920 26863410 MeRIP-seq:(Medium) rs1192406956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072633,Human_RBP_ID_22707715 Human_miRNA_ID_2394125,Human_miRNA_ID_2906025 RMVar_hsa_circ_124261,RMVar_hsa_circ_130719 63996 RMVar_ID_63996 Human_SNP_ID_7163157 m1A Human chr1 + 26994091 26994091 26994091 CGCGGCTGCGGGGGCGGGGGGCCGCGCGCTGGAGCTGGCCGAAGCACGGCGGCGGCTGCTGGAGG CGCGGCTGCGGGGGCGGGGGGCCGCGCGCTGGGGCTGGCCGAAGCACGGCGGCGGCTGCTGGAGG A G TRNP1 Ensembl:ENSG00000253368 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26994047..26994174 26863196 MeRIP-seq:(Medium) rs1233342131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350417,Human_RBP_ID_801907,Human_RBP_ID_854187,Human_RBP_ID_4072634,Human_RBP_ID_5158431,Human_RBP_ID_5234513,Human_RBP_ID_8724676,Human_RBP_ID_9410512,Human_RBP_ID_18468521,Human_RBP_ID_22026307,Human_RBP_ID_22694110,Human_RBP_ID_22707716,Human_RBP_ID_26774180 RMVar_hsa_circ_124261,RMVar_hsa_circ_130719 63997 RMVar_ID_63997 Human_SNP_ID_7163264 m1A Human chr1 + 26994412 26994412 26994412 TGCCGGGCGACTGCGGCGCGGCCACGGCCCCGAGCCCGACTCGCCCTTCCGCCGCAGCCCGCCCC TGCCGGGCGACTGCGGCGCGGCCACGGCCCCGTGCCCGACTCGCCCTTCCGCCGCAGCCCGCCCC A T TRNP1 Ensembl:ENSG00000253368 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26994362..26994531 26863196 MeRIP-seq:(Medium) rs1241681228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2579431 RMVar_hsa_circ_124261,RMVar_hsa_circ_130719 63998 RMVar_ID_63998 Human_SNP_ID_7163267 m1A Human chr1 - 26994427 26994427 26994427 GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGAAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGTAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:26994348..26994448 26863410 MeRIP-seq:(Medium) rs1443677303 Functional Loss SNV dbSNP153 33..33 33 - - - 63999 RMVar_ID_63999 Human_SNP_ID_7163268 m1A Human chr1 - 26994427 26994427 26994427 GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGAAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGGAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:26994348..26994448 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 64000 RMVar_ID_64000 Human_SNP_ID_7163269 m1A Human chr1 - 26994427 26994427 26994427 GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGAAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC GGGAGGCGGGGCCGCGGGGCGGGCTGCGGCGGCAGGGCGAGTCGGGCTCGGGGCCGTGGCCGCGC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:26994348..26994448 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 64001 RMVar_ID_64001 Human_SNP_ID_7163325 m1A Human chr1 - 26994580 26994580 26994580 CTCAGCCTCCTCTACTGGGCCCCTGGCCCCCAACTGCCTCTTCCTGCGGATCCGTAGTCCTTCCA CTCAGCCTCCTCTACTGGGCCCCTGGCCCCCAGCTGCCTCTTCCTGCGGATCCGTAGTCCTTCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26994052..26994596 32194978 MeRIP-seq:(Medium) rs919038652 Functional Loss SNV dbSNP153 33..33 33 - - - 64002 RMVar_ID_64002 Human_SNP_ID_7163326 m1A Human chr1 - 26994580 26994580 26994580 CTCAGCCTCCTCTACTGGGCCCCTGGCCCCCAACTGCCTCTTCCTGCGGATCCGTAGTCCTTCCA CTCAGCCTCCTCTACTGGGCCCCTGGCCCCCACCTGCCTCTTCCTGCGGATCCGTAGTCCTTCCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26994052..26994596 32194978 MeRIP-seq:(Medium) rs919038652 Functional Loss SNV dbSNP153 33..33 33 - - - 64003 RMVar_ID_64003 Human_SNP_ID_7197560 m1A Human chr1 - 27126002 27126002 27126002 CATGTTTGTGCTCAAGGAAAAGCAAGGAGGCCAGTAGAGCTAGGGGACAGTGAGTGGAGATTCAG CATGTTTGTGCTCAAGGAAAAGCAAGGAGGCCGGTAGAGCTAGGGGACAGTGAGTGGAGATTCAG T C SLC9A1 Ensembl:ENSG00000090020 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:27125990..27126220 26863196 MeRIP-seq:(Medium) rs1428934722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269034 64004 RMVar_ID_64004 Human_SNP_ID_7204355 m1A Human chr1 + 27155067 27155067 27155067 CGCGACGCGGCGCTCCGCCCCGGCCCAGCTGCAGCTCCTCCTGGTCCAGCTCCAGAACTAACCCT CGCGACGCGGCGCTCCGCCCCGGCCCAGCTGCGGCTCCTCCTGGTCCAGCTCCAGAACTAACCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:27154690..27155103;chr1:27154650..27155096 26863196 MeRIP-seq:(Medium) rs1366314155 Functional Loss SNV dbSNP153 33..33 33 - - - 64005 RMVar_ID_64005 Human_SNP_ID_7224461 m1A Human chr1 - 27234726 27234726 27234726 CTGCGCACCGCCTCACACCCGCGCTCACACACACTCACACTCCCTCGCGCGCTCTCACACACGCA CTGCGCACCGCCTCACACCCGCGCTCACACACCCTCACACTCCCTCGCGCGCTCTCACACACGCA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:27234676..27234846 26863196 MeRIP-seq:(Medium) rs1426450846 Functional Loss SNV dbSNP153 33..33 33 - - - 64006 RMVar_ID_64006 Human_SNP_ID_7239915 m1A Human chr1 + 27300175 27300175 27300175 TCCGAGGACTGGGTGCTCCCTCTGAGTGCTGCAGAAGGAGGCTCAGGAAGAACCTTCCCATGTCA TCCGAGGACTGGGTGCTCCCTCTGAGTGCTGCCGAAGGAGGCTCAGGAAGAACCTTCCCATGTCA A C WDTC1 Ensembl:ENSG00000142784 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27300155..27300230 26863196 MeRIP-seq:(Medium) rs530449807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47764,RMVar_hsa_circ_62462,RMVar_hsa_circ_107788,RMVar_hsa_circ_130730,RMVar_hsa_circ_93098,RMVar_hsa_circ_130731,RMVar_hsa_circ_75763,RMVar_hsa_circ_130732,RMVar_hsa_circ_123339,RMVar_hsa_circ_130736 64007 RMVar_ID_64007 Human_SNP_ID_7241566 m1A Human chr1 - 27306991 27306991 27306991 GGTGCAGGGCCAGAGCTAGTAGCCAGGAGAGGAGCGAGGGTGCTCCACAGCGACCTCAGCAGGTG GGTGCAGGGCCAGAGCTAGTAGCCAGGAGAGGGGCGAGGGTGCTCCACAGCGACCTCAGCAGGTG T C lnc-MAP3K6-1 RNACentral:URS00008B36A6 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:27306940..27307140 32194978 MeRIP-seq:(Medium) rs1171491790 Functional Loss SNV dbSNP153 33..33 33 - - - 64008 RMVar_ID_64008 Human_SNP_ID_7246559 m1A Human chr1 - 27328136 27328136 27328136 GGAGGTCTTGCCTGAACGGTGTCTTCCAGCACAGCCACCCAATCCCAGATCCCACTACAATGCTT GGAGGTCTTGCCTGAACGGTGTCTTCCAGCACGGCCACCCAATCCCAGATCCCACTACAATGCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27328134..27328398 26863196 MeRIP-seq:(Medium) rs191635605 Functional Loss SNV dbSNP153 33..33 33 - - - 64009 RMVar_ID_64009 Human_SNP_ID_7248675 m1A Human chr1 + 27336199 27336199 27336199 TAGACAGCACTCAGCCCCAGCCCCAGGTGTGGACCTCATGCTGGTGATGGCTCCCCTGGGTGGCC TAGACAGCACTCAGCCCCAGCCCCAGGTGTGGGCCTCATGCTGGTGATGGCTCCCCTGGGTGGCC A G TMEM222 Ensembl:ENSG00000186501 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:27336150..27336251 32194978 MeRIP-seq:(Medium) rs759256338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17646920,Human_RBP_ID_18157751,Human_RBP_ID_26385590 RMVar_hsa_circ_106748,RMVar_hsa_circ_130737 64010 RMVar_ID_64010 Human_SNP_ID_7255342 m1A Human chr1 + 27358422 27358422 27358422 ACTGTGCCCATCCCGCCACCCGCAAGCACCTGAGGGCCGTGGAGCATGTCGTGGGGAGCTGGGGC ACTGTGCCCATCCCGCCACCCGCAAGCACCTGCGGGCCGTGGAGCATGTCGTGGGGAGCTGGGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27358414..27358494 26863196 MeRIP-seq:(Medium) rs1355445777 Functional Loss SNV dbSNP153 33..33 33 - - - 64011 RMVar_ID_64011 Human_SNP_ID_7256144 m1A Human chr1 + 27360801 27360801 27360801 CGTACACCACCCCATACGTGCCCTTGCCCAGCACCAGCCGCTCGCCCGTCTCCGTGTACTCATAA CGTACACCACCCCATACGTGCCCTTGCCCAGCCCCAGCCGCTCGCCCGTCTCCGTGTACTCATAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27360751..27360975 26863196 MeRIP-seq:(Medium) rs764195370 Functional Loss SNV dbSNP153 33..33 33 - - - 64012 RMVar_ID_64012 Human_SNP_ID_7256145 m1A Human chr1 + 27360801 27360801 27360801 CGTACACCACCCCATACGTGCCCTTGCCCAGCACCAGCCGCTCGCCCGTCTCCGTGTACTCATAA CGTACACCACCCCATACGTGCCCTTGCCCAGCGCCAGCCGCTCGCCCGTCTCCGTGTACTCATAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27360751..27360975 26863196 MeRIP-seq:(Medium) rs764195370 Functional Loss SNV dbSNP153 33..33 33 - - - 64013 RMVar_ID_64013 Human_SNP_ID_7257085 m1A Human chr1 + 27363249 27363249 27363249 GCAGTGATCTTGGACAGCGGTGACCATACCACAGGCAGCACCACCTCCCCCACCCCGACCCAGGC GCAGTGATCTTGGACAGCGGTGACCATACCACTGGCAGCACCACCTCCCCCACCCCGACCCAGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:27363200..27363288 26863196 MeRIP-seq:(Medium) rs538957831 Functional Loss SNV dbSNP153 33..33 33 - - - 64014 RMVar_ID_64014 Human_SNP_ID_7258232 m1A Human chr1 - 27366922 27366922 27366922 AAGGCAGGGCAGCGTTGGCGGGCGCTCCCTTGAGAAGTCCAGGTGGCGGGCACCTCCGAGCCGAT AAGGCAGGGCAGCGTTGGCGGGCGCTCCCTTGGGAAGTCCAGGTGGCGGGCACCTCCGAGCCGAT T C MAP3K6 Ensembl:ENSG00000142733 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27366835..27366945 26863196 MeRIP-seq:(Medium) rs1363342849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4093343 64015 RMVar_ID_64015 Human_SNP_ID_7268226 m1A Human chr1 + 27405091 27405091 27405091 GTCACCAAAGCCACAGAGACCTCAATCTGTCCAAGCTGGCACTGCAGAGTCAGAGGATGGGCGCC GTCACCAAAGCCACAGAGACCTCAATCTGTCCGAGCTGGCACTGCAGAGTCAGAGGATGGGCGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:27404926..27405125 32194978 MeRIP-seq:(Medium) rs560669249 Functional Loss SNV dbSNP153 33..33 33 - - - 64016 RMVar_ID_64016 Human_SNP_ID_7269481 m1A Human chr1 + 27409726 27409714 27409726 TGACGGATGGCTGAAAGCAGGTCGCTACGGGCATCGCTCACGGCAGGCAAGGAGGACTTGGGCTT TGACGGATGGCTGAAAGCAGG____________TCGCTCACGGCAGGCAAGGAGGACTTGGGCTT GTCGCTACGGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:27409701..27409725 26863196 MeRIP-seq:(Medium) rs773432993 Functional Loss DEL dbSNP153 22..33 33 - - - 64017 RMVar_ID_64017 Human_SNP_ID_7269598 m1A Human chr1 + 27410050 27410050 27410050 GGCGGTGGTGGAGGTGGGATGCCTATCATTGGAGGCGGAGGTGGCGGAGGGGCAGGTGGTGGAGC GGCGGTGGTGGAGGTGGGATGCCTATCATTGGGGGCGGAGGTGGCGGAGGGGCAGGTGGTGGAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:27409751..27410125;chr1:27410001..27410075 26863196 MeRIP-seq:(Medium) rs375848071 Functional Loss SNV dbSNP153 33..33 33 - - - 64018 RMVar_ID_64018 Human_SNP_ID_7289657 m1A Human chr1 + 27490116 27490116 27490116 ACGGCCGGACCCCCTCAGCGCGCTACGCCCCCAGCCGCGCTCGCCCTGCCTGTGTCCGCCATTAC ACGGCCGGACCCCCTCAGCGCGCTACGCCCCCGGCCGCGCTCGCCCTGCCTGTGTCCGCCATTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:27428902..27490175;chr1:27489967..27490150;chr1:27489951..27490175;chr1:27489933..27490175;chr1:27490001..27490175 26863196 MeRIP-seq:(Medium) rs1048321523 Functional Loss SNV dbSNP153 33..33 33 - - - 64019 RMVar_ID_64019 Human_SNP_ID_7304807 m1A Human chr1 + 27549227 27549227 27549227 TAGCCGCCGTACTGGGGCAGGTAGGTGTTGGCAGGCGGGTGGGTGGTAGGTGAGCGGGCCATGGC TAGCCGCCGTACTGGGGCAGGTAGGTGTTGGCCGGCGGGTGGGTGGTAGGTGAGCGGGCCATGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27549178..27549410 26863196 MeRIP-seq:(Medium) rs951049067 Functional Loss SNV dbSNP153 33..33 33 - - - 64020 RMVar_ID_64020 Human_SNP_ID_7307083 m1A Human chr1 + 27556802 27556802 27556802 CGCCCTCCCCTGCAGCCTCCTACAACGGTCCTAGTCCCAACCATCAGTTCTAATTTTTGACTTCT CGCCCTCCCCTGCAGCCTCCTACAACGGTCCTCGTCCCAACCATCAGTTCTAATTTTTGACTTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27556799..27556923 26863196 MeRIP-seq:(Medium) rs1309416923 Functional Loss SNV dbSNP153 33..33 33 - - - 64021 RMVar_ID_64021 Human_SNP_ID_7307241 m1A Human chr1 - 27557335 27557335 27557335 GCAGGGAAGGCCTAGTGGGGCTGGAGGAGGGGAGTCCTCCGGGAGACAGAAGGAAAGACAAGGAC GCAGGGAAGGCCTAGTGGGGCTGGAGGAGGGGCGTCCTCCGGGAGACAGAAGGAAAGACAAGGAC T G AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27557237..27557365 26863196 MeRIP-seq:(Medium) rs1464743758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258426,Human_RBP_ID_3328220,Human_RBP_ID_5233872,Human_RBP_ID_5332903,Human_RBP_ID_8166891,Human_RBP_ID_9411035 RMVar_hsa_circ_4759 64022 RMVar_ID_64022 Human_SNP_ID_7310451 m1A Human chr1 + 27569679 27569679 27569679 TGATGCTGGCCGTCAGGAGTCATAAATGGGGCAGCGTGACAGCAGGGCCAGAACAGGCTACCTCT TGATGCTGGCCGTCAGGAGTCATAAATGGGGCGGCGTGACAGCAGGGCCAGAACAGGCTACCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27569672..27569807 26863196 MeRIP-seq:(Medium) rs1300837224 Functional Loss SNV dbSNP153 33..33 33 - - - 64023 RMVar_ID_64023 Human_SNP_ID_7313530 m1A Human chr1 - 27581904 27581902 27581904 ACGGAGTGAGTGTGTGGGTGGTGTTGAGACTCAGGGGAGGGGAAGAGAGGAGAGGAAGAAGTCAG ACGGAGTGAGTGTGTGGGTGGTGTTGAGACTC__GGGAGGGGAAGAGAGGAGAGGAAGAAGTCAG CCT C AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27581897..27582037 26863196 MeRIP-seq:(Medium) rs975122632 Functional Loss DEL dbSNP153 33..34 33 - - - 64024 RMVar_ID_64024 Human_SNP_ID_7313846 m1A Human chr1 - 27583455 27583455 27583455 CCGAGTGGGTTTTCTCAGCAATAAACAACAAGACATGAGCTCAGGGAAGGGAACAAGTGAAGTCT CCGAGTGGGTTTTCTCAGCAATAAACAACAAGGCATGAGCTCAGGGAAGGGAACAAGTGAAGTCT T C AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27583448..27583693 26863196 MeRIP-seq:(Medium) rs759959739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5803734 64025 RMVar_ID_64025 Human_SNP_ID_7314696 m1A Human chr1 - 27587328 27587324 27587328 TGGAGGCGAGGCCTCAGAGGCTAGGCTGGGAGAGGGCAGCATGGAACTGAGCCGCCCTCTGAAAA TGGAGGCGAGGCCTCAGAGGCTAGGCTGGGAG____CAGCATGGAACTGAGCCGCCCTCTGAAAA GCCCT G AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27587323..27587486 26863196 MeRIP-seq:(Medium) rs1203724223 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8052555 64026 RMVar_ID_64026 Human_SNP_ID_7316673 m1A Human chr1 - 27595282 27595282 27595282 TCTGCCCACAGCCCCCAACGTTTCTCCCAGCTATAGCTCAGCACTTCCCCAAACACCGGTATCAT TCTGCCCACAGCCCCCAACGTTTCTCCCAGCTGTAGCTCAGCACTTCCCCAAACACCGGTATCAT T C AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27595280..27595484 26863196 MeRIP-seq:(Medium) rs778392303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190219 64027 RMVar_ID_64027 Human_SNP_ID_7317351 m1A Human chr1 - 27597937 27597934 27597938 AGATGGACTGGGACAGGGAGAGACGGACAGACAGAGGTGCTGGCAGAGAGAGGAGGAGGCAGAAA AGATGGACTGGGACAGGGAGAGACGGACAGA____GGTGCTGGCAGAGAGAGGAGGAGGCAGAAA CTCTG C AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27597804..27598092 26863196 MeRIP-seq:(Medium) rs1048638310 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_258447,Human_RBP_ID_9411772,Human_RBP_ID_24550340,Human_RBP_ID_26774194 64028 RMVar_ID_64028 Human_SNP_ID_7318049 m1A Human chr1 - 27600710 27600710 27600710 CACCTGATTGCTGTGGTTGTGCTGGAGGCTTGAGGGGCAGACTGCCCCTGGCAGAAGACATTTGG CACCTGATTGCTGTGGTTGTGCTGGAGGCTTGTGGGGCAGACTGCCCCTGGCAGAAGACATTTGG T A AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:27600707..27600823 32194978 MeRIP-seq:(Medium) rs1185653590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328254,Human_RBP_ID_8051694 64029 RMVar_ID_64029 Human_SNP_ID_7318990 m1A Human chr1 - 27603943 27603943 27603943 CAGAAGGCAGGAGGAGGGAGGGGAGGAGGGGGAGGGAGGGAGAGAGGGAATCCAGCTACCACCAC CAGAAGGCAGGAGGAGGGAGGGGAGGAGGGGGGGGGAGGGAGAGAGGGAATCCAGCTACCACCAC T C AHDC1 Ensembl:ENSG00000126705 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:27603843..27604104 26863196 MeRIP-seq:(Medium) rs1489591901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257,Human_RBP_ID_8166938,Human_RBP_ID_8227971,Human_RBP_ID_9410523,Human_RBP_ID_18928169,Human_RBP_ID_26774200 64030 RMVar_ID_64030 Human_SNP_ID_7319053 m1A Human chr1 - 27604107 27604107 27604107 CAGCGGCGGCGGCGGCGGAGACGGAGAGAGGCAGGCAGGCAGGGCGAGGGCGAGAGACGGAGGGA CAGCGGCGGCGGCGGCGGAGACGGAGAGAGGCTGGCAGGCAGGGCGAGGGCGAGAGACGGAGGGA T A AHDC1 Ensembl:ENSG00000126705 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27603361..27604175 26863196 MeRIP-seq:(Medium) rs1359695420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26774201 64031 RMVar_ID_64031 Human_SNP_ID_7334701 m1A Human chr1 + 27666154 27666154 27666154 ACAAAGTTCTGGATTCTGGGCATCGTCGGCGCATGCTTGTAATCCTACTTGGGAGGTTGAGACAG ACAAAGTTCTGGATTCTGGGCATCGTCGGCGCGTGCTTGTAATCCTACTTGGGAGGTTGAGACAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27666103..27666223 26863196 MeRIP-seq:(Medium) rs1276941793 Functional Loss SNV dbSNP153 33..33 33 - - - 64032 RMVar_ID_64032 Human_SNP_ID_7335640 m1A Human chr1 + 27669183 27669183 27669183 GCATCCTTACCCGCATCCTTACCTGCACCCTTACTTGCATCCTTACCTGCACCCTTACCTGTCCC GCATCCTTACCCGCATCCTTACCTGCACCCTTCCTTGCATCCTTACCTGCACCCTTACCTGTCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:27669180..27669262 26863196 MeRIP-seq:(Medium) rs1362898008 Functional Loss SNV dbSNP153 33..33 33 - - - 64033 RMVar_ID_64033 Human_SNP_ID_7336328 m1A Human chr1 + 27672063 27672063 27672063 CCTGGCTCTCAGAACATGAGATTTACAGGCAGACAGGCAGCCTGGCAGAGGGTGGCAGCTTGATG CCTGGCTCTCAGAACATGAGATTTACAGGCAGTCAGGCAGCCTGGCAGAGGGTGGCAGCTTGATG A T AL445490.1 Ensembl:ENSG00000225886 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27672060..27672165 26863196 MeRIP-seq:(Medium) rs942241831 Functional Loss SNV dbSNP153 33..33 33 - - - 64034 RMVar_ID_64034 Human_SNP_ID_7373958 m1A Human chr1 - 27830873 27830873 27830873 GCCCCGCCACTCACCAGGTTGGGCAGTCGAACAGCGGGAGGCTAGAGCCGGAGTTCGCGGCTGCC GCCCCGCCACTCACCAGGTTGGGCAGTCGAACGGCGGGAGGCTAGAGCCGGAGTTCGCGGCTGCC T C AL020997.4 Ensembl:ENSG00000286433 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27830801..27830976 26863196 MeRIP-seq:(Medium) rs1044865954 Functional Loss SNV dbSNP153 33..33 33 - - - 64035 RMVar_ID_64035 Human_SNP_ID_7394107 m1A Human chr1 + 27907033 27907033 27907033 GGAGCCTTCTCTGCATGTCTGATGATCCCCACAATAGTGACCTAGGTTAGAAGAAACAAAGAAAA GGAGCCTTCTCTGCATGTCTGATGATCCCCACGATAGTGACCTAGGTTAGAAGAAACAAAGAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:27894075..27907039 32194978 MeRIP-seq:(Medium) rs759856284 Functional Loss SNV dbSNP153 33..33 33 - - - 64036 RMVar_ID_64036 Human_SNP_ID_7396063 m1A Human chr1 + 27914473 27914473 27914473 CATCTTGGTCACGATTCTCCGCAAAGAGGCCGAGAAGGTGCGGGTCTGGGGGAATAGCGGAAAAC CATCTTGGTCACGATTCTCCGCAAAGAGGCCGGGAAGGTGCGGGTCTGGGGGAATAGCGGAAAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:27914450..27914549 32194978 MeRIP-seq:(Medium) rs1334177671 Functional Loss SNV dbSNP153 33..33 33 - - - 64037 RMVar_ID_64037 Human_SNP_ID_7396075 m1A Human chr1 - 27914487 27914487 27914487 GGCCGCGTTCTGTGGTTTTCCGCTATTCCCCCAGACCCGCACCTTCTCGGCCTCTTTGCGGAGAA GGCCGCGTTCTGTGGTTTTCCGCTATTCCCCCTGACCCGCACCTTCTCGGCCTCTTTGCGGAGAA T A RPA2 Ensembl:ENSG00000117748 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:27914219..27914488 26863196 MeRIP-seq:(Medium) rs1482947386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350848,Human_RBP_ID_742302,Human_RBP_ID_1428197,Human_RBP_ID_4042472,Human_RBP_ID_5312413,Human_RBP_ID_5457450,Human_RBP_ID_8940124,Human_RBP_ID_8968392,Human_RBP_ID_9318771,Human_RBP_ID_18414906,Human_RBP_ID_22023049,Human_RBP_ID_23384539 Human_Splice_Rec_36827,Human_Splice_Rec_36881 Human_miRNA_ID_2142782,Human_miRNA_ID_2144317,Human_miRNA_ID_2686823,Human_miRNA_ID_2944681 RMVar_hsa_circ_96066,RMVar_hsa_circ_130781 64038 RMVar_ID_64038 Human_SNP_ID_7396088 m1A Human chr1 + 27914501 27914501 27914501 GCCGAGAAGGTGCGGGTCTGGGGGAATAGCGGAAAACCACAGAACGCGGCCGCCACTGCGCCGCT GCCGAGAAGGTGCGGGTCTGGGGGAATAGCGGTAAACCACAGAACGCGGCCGCCACTGCGCCGCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:27914186..27914550 26863196 MeRIP-seq:(Medium) rs1158816560 Functional Loss SNV dbSNP153 33..33 33 - - - 64039 RMVar_ID_64039 Human_SNP_ID_7396090 m1A Human chr1 + 27914507 27914507 27914507 AAGGTGCGGGTCTGGGGGAATAGCGGAAAACCACAGAACGCGGCCGCCACTGCGCCGCTCTGGCT AAGGTGCGGGTCTGGGGGAATAGCGGAAAACCGCAGAACGCGGCCGCCACTGCGCCGCTCTGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:27914192..27914707 26863196 MeRIP-seq:(Medium) rs1443110808 Functional Loss SNV dbSNP153 33..33 33 - - - 64040 RMVar_ID_64040 Human_SNP_ID_7396112 m1A Human chr1 - 27914547 27914547 27914547 CGCCATTCGCGGGAAGGCGTTTGTGGTGCCAGAGAAAAGTAGCCAGAGCGGCGCAGTGGCGGCCG CGCCATTCGCGGGAAGGCGTTTGTGGTGCCAGGGAAAAGTAGCCAGAGCGGCGCAGTGGCGGCCG T C RPA2 Ensembl:ENSG00000117748 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:27914276..27914550 26863196 MeRIP-seq:(Medium) rs902927436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073759 RMVar_hsa_circ_96066,RMVar_hsa_circ_130781 64041 RMVar_ID_64041 Human_SNP_ID_7396157 m1A Human chr1 - 27914649 27914649 27914649 GCAGTACGCGTTTTCTGGAGCATGGGCAGAGGAGACAGGAACAAGCGTAGCATCCGTGAGCACCG GCAGTACGCGTTTTCTGGAGCATGGGCAGAGGCGACAGGAACAAGCGTAGCATCCGTGAGCACCG T G RPA2 Ensembl:ENSG00000117748 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:27914606..27914703 26863196 MeRIP-seq:(Medium) rs753713321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22023050 Human_Splice_Rec_36851 RMVar_hsa_circ_96066,RMVar_hsa_circ_130781 64042 RMVar_ID_64042 Human_SNP_ID_7437369 m1A Human chr1 + 28088574 28088574 28088574 CCACAACAGGACATGGAGATCAGTCCAGACCCACAGTAGAACCAATCGAGCGGAGGAAACCGCGG CCACAACAGGACATGGAGATCAGTCCAGACCCGCAGTAGAACCAATCGAGCGGAGGAAACCGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28088493..28088605 26863196 MeRIP-seq:(Medium) rs1361034842 Functional Loss SNV dbSNP153 33..33 33 - - - 64043 RMVar_ID_64043 Human_SNP_ID_7439242 m1A Human chr1 - 28096313 28096313 28096313 CGGGACAGGGAGTGGCCGTAGCGGCTTGTTGGATAAGTGGAAGATAGATGATAAGCCTGTAAAAA CGGGACAGGGAGTGGCCGTAGCGGCTTGTTGGGTAAGTGGAAGATAGATGATAAGCCTGTAAAAA T C SPCS2P4 Ensembl:ENSG00000228589 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28096213..28096373 26863196 MeRIP-seq:(Medium) rs775561889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1428215,Human_RBP_ID_4042634,Human_RBP_ID_5804641,Human_RBP_ID_10912963,Human_RBP_ID_23384716 64044 RMVar_ID_64044 Human_SNP_ID_7439244 m1A Human chr1 + 28096317 28096317 28096317 TACAGGCTTATCATCTATCTTCCACTTATCCAACAAGCCGCTACGGCCACTCCCTGTCCCGCAGT TACAGGCTTATCATCTATCTTCCACTTATCCAGCAAGCCGCTACGGCCACTCCCTGTCCCGCAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28096286..28096386 26863196 MeRIP-seq:(Medium) rs56393783 Functional Loss SNV dbSNP153 33..33 33 - - - 64045 RMVar_ID_64045 Human_SNP_ID_7464352 m1A Human chr1 - 28200696 28200692 28200696 GTGTTTGGCATGTGCCCCCTGTCTACTGACCAATCAGTGTGGCATGAGGCCCACGCCACCCAAAC GTGTTTGGCATGTGCCCCCTGTCTACTGACCA____GTGTGGCATGAGGCCCACGCCACCCAAAC CTGAT C DNAJC8 Ensembl:ENSG00000126698 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:28200626..28201025 32194978 MeRIP-seq:(Medium) rs760832249 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_350920,Human_RBP_ID_4093494,Human_RBP_ID_17223770,Human_RBP_ID_26860929 Human_miRNA_ID_244836,Human_miRNA_ID_247339,Human_miRNA_ID_1503611 64046 RMVar_ID_64046 Human_SNP_ID_7464353 m1A Human chr1 - 28200696 28200696 28200696 GTGTTTGGCATGTGCCCCCTGTCTACTGACCAATCAGTGTGGCATGAGGCCCACGCCACCCAAAC GTGTTTGGCATGTGCCCCCTGTCTACTGACCAGTCAGTGTGGCATGAGGCCCACGCCACCCAAAC T C DNAJC8 Ensembl:ENSG00000126698 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:28200626..28201025 32194978 MeRIP-seq:(Medium) rs769480841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350920,Human_RBP_ID_4093494,Human_RBP_ID_17223770,Human_RBP_ID_26860929 Human_miRNA_ID_244836,Human_miRNA_ID_247339,Human_miRNA_ID_1503611 64047 RMVar_ID_64047 Human_SNP_ID_7472623 m1A Human chr1 - 28232969 28232969 28232969 GAAATGGCGGCTTCAGGAGAGAGCGGGACTTCAGGCGGCGGAGGCAGCACCGAGGAAGCATTTAT GAAATGGCGGCTTCAGGAGAGAGCGGGACTTCGGGCGGCGGAGGCAGCACCGAGGAAGCATTTAT T C DNAJC8 Ensembl:ENSG00000126698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:28232893..28233025;chr1:28232872..28233025;chr1:28228901..28233025 26863196 MeRIP-seq:(Medium) rs777415384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223875,Human_RBP_ID_350956,Human_RBP_ID_746435,Human_RBP_ID_977322,Human_RBP_ID_4042671,Human_RBP_ID_5457456,Human_RBP_ID_5486011,Human_RBP_ID_5804782,Human_RBP_ID_8968430,Human_RBP_ID_9355850,Human_RBP_ID_10913800,Human_RBP_ID_23384806,Human_RBP_ID_26309692,Human_RBP_ID_26860955 Human_Splice_Rec_37201,Human_Splice_Rec_37217,Human_Splice_Rec_37237,Human_Splice_Rec_37243 64048 RMVar_ID_64048 Human_SNP_ID_7473550 m1A Human chr1 + 28236184 28236182 28236185 GCAGAGACGCCAGAGGTGCAGCTCCAGCAGCAATGGCAGTGACGGCGTTGGCGGCGCGGACGTGG GCAGAGACGCCAGAGGTGCAGCTCCAGCAGC___GGCAGTGACGGCGTTGGCGGCGCGGACGTGG CAAT C ATP5IF1 Ensembl:ENSG00000130770 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:28236101..28236940;chr1:28236126..28236925 26863196 MeRIP-seq:(Medium) rs1269534830 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4073763,Human_RBP_ID_5457457,Human_RBP_ID_8968431,Human_RBP_ID_9318772,Human_RBP_ID_9358465,Human_RBP_ID_10913802,Human_RBP_ID_18430081,Human_RBP_ID_23384810,Human_RBP_ID_26860959 Human_Splice_Rec_37251,Human_Splice_Rec_37255,Human_Splice_Rec_37259,Human_Splice_Rec_37263 64049 RMVar_ID_64049 Human_SNP_ID_7473582 m1A Human chr1 + 28236252 28236252 28236252 GGCGTGTGGGGCGTGAGGACCATGCAAGCCCGAGGCTTCGGCTCGGATCAGGTACGCTGCGGCAG GGCGTGTGGGGCGTGAGGACCATGCAAGCCCGGGGCTTCGGCTCGGATCAGGTACGCTGCGGCAG A G ATP5IF1 Ensembl:ENSG00000130770 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr1:28236126..28236519;chr1:28236201..28236275 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_350962,Human_RBP_ID_746468,Human_RBP_ID_4073763,Human_RBP_ID_5108523,Human_RBP_ID_9318772,Human_RBP_ID_9358465,Human_RBP_ID_10913808,Human_RBP_ID_18967736,Human_RBP_ID_22429175,Human_RBP_ID_26310665 Human_Splice_Rec_37251,Human_Splice_Rec_37255,Human_Splice_Rec_37259,Human_Splice_Rec_37263 64050 RMVar_ID_64050 Human_SNP_ID_7473673 m1A Human chr1 + 28236421 28236421 28236421 CCATCCGGGAAGCCGGTGGGGCCTTCGGAAAGAGAGAGCAGGCTGAAGAGGAACGATATTTCCGG CCATCCGGGAAGCCGGTGGGGCCTTCGGAAAGGGAGAGCAGGCTGAAGAGGAACGATATTTCCGG A G ATP5IF1 Ensembl:ENSG00000130770 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:28236126..28236450 26863196 MeRIP-seq:(Medium) rs1172470953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350966,Human_RBP_ID_1744482,Human_RBP_ID_4042681,Human_RBP_ID_5804786,Human_RBP_ID_9355851,Human_RBP_ID_10913809,Human_RBP_ID_17646311,Human_RBP_ID_18967737,Human_RBP_ID_19034384,Human_RBP_ID_22427035,Human_RBP_ID_23384814 Human_Splice_Rec_37252,Human_Splice_Rec_37253,Human_Splice_Rec_37256,Human_Splice_Rec_37257,Human_Splice_Rec_37260,Human_Splice_Rec_37261,Human_Splice_Rec_37264 RMVar_hsa_circ_105057,RMVar_hsa_circ_130822 64051 RMVar_ID_64051 Human_SNP_ID_7473690 m1A Human chr1 - 28236454 28236454 28236454 TCCAGGGCTGGACTTGGGACCCGGTGAGCCTCACCGGAAATATCGTTCCTCTTCAGCCTGCTCTC TCCAGGGCTGGACTTGGGACCCGGTGAGCCTCCCCGGAAATATCGTTCCTCTTCAGCCTGCTCTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:28236351..28236475 32194978 MeRIP-seq:(Medium) rs113339056 Functional Loss SNV dbSNP153 33..33 33 - - - 64052 RMVar_ID_64052 Human_SNP_ID_7473782 m1A Human chr1 + 28236713 28236713 28236713 CACCGGCGGGTCTCCAAAACAACCCACGGCTCAACTCCTCCTTTATCATTACCATCTCCCGCGTG CACCGGCGGGTCTCCAAAACAACCCACGGCTCGACTCCTCCTTTATCATTACCATCTCCCGCGTG A G ATP5IF1 Ensembl:ENSG00000130770 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:28236709..28236834 26863410 MeRIP-seq:(Medium) rs1434166230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3308873,Human_RBP_ID_17071826,Human_RBP_ID_17217720,Human_RBP_ID_17335071,Human_RBP_ID_17452146,Human_RBP_ID_17747792,Human_RBP_ID_22020036,Human_RBP_ID_23261999 RMVar_hsa_circ_105057,RMVar_hsa_circ_130822 64053 RMVar_ID_64053 Human_SNP_ID_7474047 m1A Human chr1 - 28237784 28237784 28237784 AGGGTTTAATTTCAATCCTTCACCCCAAAGAGATCTCAAAGCATAACCTGTAATGTCTAAGCAAG AGGGTTTAATTTCAATCCTTCACCCCAAAGAGTTCTCAAAGCATAACCTGTAATGTCTAAGCAAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28237782..28237976 26863196 MeRIP-seq:(Medium) rs1411532640 Functional Loss SNV dbSNP153 33..33 33 - - - 64054 RMVar_ID_64054 Human_SNP_ID_7508415 m1A Human chr1 + 28369818 28369818 28369818 GGCTGCTGTGGAGGCTGAGGAGGCGGCGGCGGAGATCTGGGTAAGTTCAGCGAGCAAGGGAAAGT GGCTGCTGTGGAGGCTGAGGAGGCGGCGGCGGCGATCTGGGTAAGTTCAGCGAGCAAGGGAAAGT A C PHACTR4 Ensembl:ENSG00000204138 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28369775..28369890 26863196 MeRIP-seq:(Medium) rs557691929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075341,Human_RBP_ID_18414908,Human_RBP_ID_18967739,Human_RBP_ID_19034393,Human_RBP_ID_22871586 Human_Splice_Rec_37301,Human_Splice_Rec_37309,Human_Splice_Rec_37321,Human_Splice_Rec_37349,Human_Splice_Rec_37359,Human_Splice_Rec_37385 64055 RMVar_ID_64055 Human_SNP_ID_7510828 m1A Human chr1 + 28378677 28378677 28378677 TTTGTTTTGATTTTAAGGATGGGAGAGGTTTGACATGTTTGAAGGGAAAGGGAAAGCAGCCAGCA TTTGTTTTGATTTTAAGGATGGGAGAGGTTTGCCATGTTTGAAGGGAAAGGGAAAGCAGCCAGCA A C PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28378675..28378871 26863196 MeRIP-seq:(Medium) rs1203448212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10914864 64056 RMVar_ID_64056 Human_SNP_ID_7515000 m1A Human chr1 + 28394270 28394268 28394270 AAGTTTTAGAAAGTAAAAAAAAAAAAAAAAGAAAGAGGGACGGAGGGAAGGAAAGGAGGGAGGGA AAGTTTTAGAAAGTAAAAAAAAAAAAAAAAG__AGAGGGACGGAGGGAAGGAAAGGAGGGAGGGA GAA G PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28394260..28394361 26863196 MeRIP-seq:(Medium) rs964433361 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17066516 RMVar_hsa_circ_130834,RMVar_hsa_circ_282035 64057 RMVar_ID_64057 Human_SNP_ID_7534466 m1A Human chr1 + 28473687 28473672 28473687 GAGTCTGCTGCTGCCATCACCACAAAAACACCAAGTGATGAAAGAGAGAAGAGCACGTGTTCTAT GAGTCTGCTGCTGCCATC_______________AGTGATGAAAGAGAGAAGAGCACGTGTTCTAT CACCACAAAAACACCA C PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28473640..28473812 26863196 MeRIP-seq:(Medium) rs1264833341 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_351064,Human_RBP_ID_17217754,Human_RBP_ID_26797995 Human_miRNA_ID_2478036,Human_miRNA_ID_2478037,Human_miRNA_ID_3115446,Human_miRNA_ID_3115447 RMVar_hsa_circ_11475,RMVar_hsa_circ_71399,RMVar_hsa_circ_58797,RMVar_hsa_circ_130843,RMVar_hsa_circ_112572,RMVar_hsa_circ_272417,RMVar_hsa_circ_290612,RMVar_hsa_circ_369863,RMVar_hsa_circ_281768,RMVar_hsa_circ_116363,RMVar_hsa_circ_130845,RMVar_hsa_circ_130846,RMVar_hsa_circ_130847,RMVar_hsa_circ_130844,RMVar_hsa_circ_130842 64058 RMVar_ID_64058 Human_SNP_ID_7541054 m1A Human chr1 + 28498974 28498974 28498974 TCTGTAATCCCAACTACTCAGGACGCTGAGGCAGGAGAGTCGCTTGAACCCAGGAGGCGGAGATT TCTGTAATCCCAACTACTCAGGACGCTGAGGCGGGAGAGTCGCTTGAACCCAGGAGGCGGAGATT A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1354738099 Functional Loss SNV dbSNP153 33..33 33 - - - 64059 RMVar_ID_64059 Human_SNP_ID_7543165 m1A Human chr1 - 28506520 28506520 28506520 GCGTACTTTAGAGTTGGGACCGATGCCGCCTAAGACACCCATATATAGTTTTAAATTACATGATT GCGTACTTTAGAGTTGGGACCGATGCCGCCTATGACACCCATATATAGTTTTAAATTACATGATT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28506511..28506643 26863196 MeRIP-seq:(Medium) rs762954319 Functional Loss SNV dbSNP153 33..33 33 - - - 64060 RMVar_ID_64060 Human_SNP_ID_7543170 m1A Human chr1 - 28506548 28506538 28506548 GCCCACTTCTGGCCCAGGCCCGTCTAACGCGTACTTTAGAGTTGGGACCGATGCCGCCTAAGACA GCCCACTTCTGGCCCAGGCCCGTCTAACGCGT__________TGGGACCGATGCCGCCTAAGACA AACTCTAAAGT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:28506426..28506800 26863196 MeRIP-seq:(Medium) rs999602603 Functional Loss DEL dbSNP153 33..42 33 - - - 64061 RMVar_ID_64061 Human_SNP_ID_7543172 m1A Human chr1 + 28506539 28506539 28506539 ATATATGGGTGTCTTAGGCGGCATCGGTCCCAACTCTAAAGTACGCGTTAGACGGGCCTGGGCCA ATATATGGGTGTCTTAGGCGGCATCGGTCCCAGCTCTAAAGTACGCGTTAGACGGGCCTGGGCCA A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28506521..28506613 26863196 MeRIP-seq:(Medium) rs1432666380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092425,Human_RBP_ID_5544112,Human_RBP_ID_5805437,Human_RBP_ID_10916361 RMVar_hsa_circ_127108,RMVar_hsa_circ_90562,RMVar_hsa_circ_130862,RMVar_hsa_circ_130863 64062 RMVar_ID_64062 Human_SNP_ID_7544699 m1A Human chr1 + 28510171 28510170 28510171 AGCCGTTAAGCCATTTGGAACTTGATGGAGACAGGTTTGAGGGAGGTGGGTGAGATTGGAGTTTG AGCCGTTAAGCCATTTGGAACTTGATGGAGAC_GGTTTGAGGGAGGTGGGTGAGATTGGAGTTTG CA C RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28510120..28510280 26863196 MeRIP-seq:(Medium) rs1361465206 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5805584,Human_RBP_ID_10916641,Human_RBP_ID_23385147,Human_RBP_ID_27835123 Human_miRNA_ID_2014514,Human_miRNA_ID_2516060,Human_miRNA_ID_3150803,Human_miRNA_ID_3180162 RMVar_hsa_circ_127108,RMVar_hsa_circ_35000,RMVar_hsa_circ_122034,RMVar_hsa_circ_90562,RMVar_hsa_circ_130862,RMVar_hsa_circ_130863,RMVar_hsa_circ_71527,RMVar_hsa_circ_85472,RMVar_hsa_circ_130865,RMVar_hsa_circ_130866 64063 RMVar_ID_64063 Human_SNP_ID_7544731 m1A Human chr1 - 28510239 28510239 28510239 AGTAACTAGCTTCCATTCTCAAACCAACCCTGACCTCAACACCTTGGCAAGCAAGCTCTACAGTC AGTAACTAGCTTCCATTCTCAAACCAACCCTGGCCTCAACACCTTGGCAAGCAAGCTCTACAGTC T C lnc-TAF12-2 RNACentral:URS00008C404A lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:28510073..28510300;chr1:28510062..28510275 26863196 MeRIP-seq:(Medium) rs1323854998 Functional Loss SNV dbSNP153 33..33 33 - - - 64064 RMVar_ID_64064 Human_SNP_ID_7546917 m1A Human chr1 - 28516800 28516800 28516800 CTCTTTTGGATGATGTACTGTGAAATTTCTCCAACTTTTAACCCTGGGATCTCTGATCTCTCTCT CTCTTTTGGATGATGTACTGTGAAATTTCTCCGACTTTTAACCCTGGGATCTCTGATCTCTCTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28516749..28516890 26863196 MeRIP-seq:(Medium) rs763026790 Functional Loss SNV dbSNP153 33..33 33 - - - 64065 RMVar_ID_64065 Human_SNP_ID_7546920 m1A Human chr1 - 28516810 28516810 28516810 TCATGGACTCCTCTTTTGGATGATGTACTGTGAAATTTCTCCAACTTTTAACCCTGGGATCTCTG TCATGGACTCCTCTTTTGGATGATGTACTGTGGAATTTCTCCAACTTTTAACCCTGGGATCTCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28516726..28516931 26863196 MeRIP-seq:(Medium) rs1441929995 Functional Loss SNV dbSNP153 33..33 33 - - - 64066 RMVar_ID_64066 Human_SNP_ID_7547312 m1A Human chr1 - 28518300 28518300 28518300 CCGCGCGTCCCAGGCGAGACCTACCTTGGTGCACGTCGGCCACAAGGAACTCCGGCGCTCCCCGC CCGCGCGTCCCAGGCGAGACCTACCTTGGTGCCCGTCGGCCACAAGGAACTCCGGCGCTCCCCGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28518251..28518437 26863196 MeRIP-seq:(Medium) rs1360792255 Functional Loss SNV dbSNP153 33..33 33 - - - 64067 RMVar_ID_64067 Human_SNP_ID_7547603 m1A Human chr1 + 28519188 28519188 28519188 TGAGGGTAGTGGGATTAGGGTGATACAGGCAGAGGGATTGCACGTGCAACGGCATGAAGGTATAG TGAGGGTAGTGGGATTAGGGTGATACAGGCAGGGGGATTGCACGTGCAACGGCATGAAGGTATAG A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28519183..28519314 26863196 MeRIP-seq:(Medium) rs28473560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5312416,Human_RBP_ID_5805696,Human_RBP_ID_10917020,Human_RBP_ID_26774214 RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_130867 64068 RMVar_ID_64068 Human_SNP_ID_7550433 m1A Human chr1 + 28529936 28529936 28529936 CAGCAGATGCCATCCCCAAAAGCAAGAAGGTGAAGGGTAAGTTGGCCTTGGCCTCTTTGTGGGTA CAGCAGATGCCATCCCCAAAAGCAAGAAGGTGGAGGGTAAGTTGGCCTTGGCCTCTTTGTGGGTA A G RCC1 Ensembl:ENSG00000180198 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28529846..28529991 26863196 MeRIP-seq:(Medium) rs1440234252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18967745 Human_Splice_Rec_37456,Human_Splice_Rec_37457,Human_Splice_Rec_37480,Human_Splice_Rec_37481,Human_Splice_Rec_37504,Human_Splice_Rec_37505,Human_Splice_Rec_37522,Human_Splice_Rec_37523,Human_Splice_Rec_37542,Human_Splice_Rec_37543,Human_Splice_Rec_37562,Human_Splice_Rec_37563,Human_Splice_Rec_37574,Human_Splice_Rec_37575,Human_Splice_Rec_37592,Human_Splice_Rec_37593,Human_Splice_Rec_37612,Human_Splice_Rec_37613,Human_Splice_Rec_37629,Human_Splice_Rec_37633 RMVar_hsa_circ_26608,RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_106070,RMVar_hsa_circ_130867,RMVar_hsa_circ_37050,RMVar_hsa_circ_130868 64069 RMVar_ID_64069 Human_SNP_ID_7550609 m1A Human chr1 - 28530486 28530486 28530486 AAAAGACAGACACTGTCTGAGCGTGGGTCCACACTTCCCCTCCCAGTTTGGTGCTGGCTTTTCTC AAAAGACAGACACTGTCTGAGCGTGGGTCCACGCTTCCCCTCCCAGTTTGGTGCTGGCTTTTCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28530484..28530575 26863196 MeRIP-seq:(Medium) rs1447407782 Functional Loss SNV dbSNP153 33..33 33 - - - 64070 RMVar_ID_64070 Human_SNP_ID_7550618 m1A Human chr1 + 28530503 28530499 28530503 AACTGGGAGGGGAAGTGTGGACCCACGCTCAGACAGTGTCTGTCTTTTGCAGACACGAGGGCCGC AACTGGGAGGGGAAGTGTGGACCCACGCT____CAGTGTCTGTCTTTTGCAGACACGAGGGCCGC TCAGA T RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28530501..28530600 26863196 MeRIP-seq:(Medium) rs1464976223 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_37615,Human_Splice_Rec_37631 RMVar_hsa_circ_26608,RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_106070,RMVar_hsa_circ_130867,RMVar_hsa_circ_37050,RMVar_hsa_circ_130868 64071 RMVar_ID_64071 Human_SNP_ID_7551126 m1A Human chr1 + 28531820 28531820 28531820 TTCTTCACCCTTCAGTCTCACACAGGTCCCACAGCACAGAACCCGGCTTGGTGCTGACACTAGGC TTCTTCACCCTTCAGTCTCACACAGGTCCCACGGCACAGAACCCGGCTTGGTGCTGACACTAGGC A G RCC1 Ensembl:ENSG00000180198 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:28531801..28532029;chr1:28531801..28532036 26863196 MeRIP-seq:(Medium) rs368233349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351170,Human_RBP_ID_1428455,Human_RBP_ID_5805811,Human_RBP_ID_18584393,Human_RBP_ID_22783956,Human_RBP_ID_24451954,Human_RBP_ID_26586763,Human_RBP_ID_26861211 Human_Splice_Rec_37458,Human_Splice_Rec_37484,Human_Splice_Rec_37506,Human_Splice_Rec_37524,Human_Splice_Rec_37544,Human_Splice_Rec_37564,Human_Splice_Rec_37576,Human_Splice_Rec_37596,Human_Splice_Rec_37616,Human_Splice_Rec_37632,Human_Splice_Rec_37634 RMVar_hsa_circ_26608,RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_106070,RMVar_hsa_circ_130867,RMVar_hsa_circ_34218,RMVar_hsa_circ_130868,RMVar_hsa_circ_130869,RMVar_hsa_circ_335198 64072 RMVar_ID_64072 Human_SNP_ID_7551142 m1A Human chr1 - 28531863 28531863 28531863 CCATCACATTCTCACCCAGCCCCAGCTGGCCCACGTCGCCCTGGCCTAGTGTCAGCACCAAGCCG CCATCACATTCTCACCCAGCCCCAGCTGGCCCGCGTCGCCCTGGCCTAGTGTCAGCACCAAGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28531776..28532028 26863196 MeRIP-seq:(Medium) rs746176446 Functional Loss SNV dbSNP153 33..33 33 - - - 64073 RMVar_ID_64073 Human_SNP_ID_7551261 m1A Human chr1 - 28532253 28532253 28532253 CTGACACCTGTACCACCTTCTCTTGCAGCTCCACTTTCCCAGGGACCATCTCCGAGCCCTCCACT CTGACACCTGTACCACCTTCTCTTGCAGCTCCGCTTTCCCAGGGACCATCTCCGAGCCCTCCACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28532151..28532325 26863196 MeRIP-seq:(Medium) rs552405429 Functional Loss SNV dbSNP153 33..33 33 - - - 64074 RMVar_ID_64074 Human_SNP_ID_7552443 m1A Human chr1 + 28535915 28535915 28535915 TCCCCAAGTGTGTGATGCTGAAATCCAGGGGAAGCCGGGGCCACGTGAGATTCCAGGATGCCTTT TCCCCAAGTGTGTGATGCTGAAATCCAGGGGACGCCGGGGCCACGTGAGATTCCAGGATGCCTTT A C RCC1 Ensembl:ENSG00000180198 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28535849..28535978 26863196 MeRIP-seq:(Medium) rs765897836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351188,Human_RBP_ID_977417,Human_RBP_ID_1744633,Human_RBP_ID_8307415,Human_RBP_ID_17747965,Human_RBP_ID_18965098,Human_RBP_ID_22487794,Human_RBP_ID_22558356,Human_RBP_ID_23385206 Human_Splice_Rec_37466,Human_Splice_Rec_37492,Human_Splice_Rec_37514,Human_Splice_Rec_37534,Human_Splice_Rec_37552,Human_Splice_Rec_37572,Human_Splice_Rec_37584,Human_Splice_Rec_37604,Human_Splice_Rec_37624,Human_Splice_Rec_37642,Human_Splice_Rec_37654 RMVar_hsa_circ_35000 64075 RMVar_ID_64075 Human_SNP_ID_7552689 m1A Human chr1 + 28536796 28536796 28536796 GGCCGGGCTGAGTATGGGCGGCTGGGCCTTGGAGAGGGTGCTGAGGAGAAGAGCATACCCACCCT GGCCGGGCTGAGTATGGGCGGCTGGGCCTTGGGGAGGGTGCTGAGGAGAAGAGCATACCCACCCT A G RCC1 Ensembl:ENSG00000180198 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28536726..28536936 26863196 MeRIP-seq:(Medium) rs1159844723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_977422,Human_RBP_ID_5137449,Human_RBP_ID_5805838,Human_RBP_ID_8747798,Human_RBP_ID_17747972,Human_RBP_ID_18430104,Human_RBP_ID_18571169 Human_Splice_Rec_37470,Human_Splice_Rec_37496,Human_Splice_Rec_37556,Human_Splice_Rec_37588,Human_Splice_Rec_37608,Human_Splice_Rec_37628,Human_Splice_Rec_37656 64076 RMVar_ID_64076 Human_SNP_ID_7553071 m1A Human chr1 + 28538254 28538254 28538254 GGGGGTTTTCAAAAGGAACATGGCTCACTCAGAGCTATATGGTTAGACGTTTCTCCCCTTTTCCC GGGGGTTTTCAAAAGGAACATGGCTCACTCAGGGCTATATGGTTAGACGTTTCTCCCCTTTTCCC A G RCC1 Ensembl:ENSG00000180198 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:28538203..28538353 32194978 MeRIP-seq:(Medium) rs922237958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351206,Human_RBP_ID_977427,Human_RBP_ID_1233627,Human_RBP_ID_1347994,Human_RBP_ID_1428495,Human_RBP_ID_1744644,Human_RBP_ID_17217772,Human_RBP_ID_17335108,Human_RBP_ID_17452197,Human_RBP_ID_17646924,Human_RBP_ID_17747985,Human_RBP_ID_22783984,Human_RBP_ID_26378668,Human_RBP_ID_27180810 Human_miRNA_ID_879955 64077 RMVar_ID_64077 Human_SNP_ID_7553200 m1A Human chr1 - 28538788 28538782 28538788 TCAATCCCCCACCTCCTTTCAATATTGCTGTTAAGTTTGTTTATAAAACCCTCCACCCTCTCTCC TCAATCCCCCACCTCCTTTCAATATTGCTGTT______GTTTATAAAACCCTCCACCCTCTCTCC CAAACTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28538738..28538823 26863196 MeRIP-seq:(Medium) rs1322268691 Functional Loss DEL dbSNP153 33..38 33 - - - 64078 RMVar_ID_64078 Human_SNP_ID_7553203 m1A Human chr1 - 28538788 28538786 28538788 TCAATCCCCCACCTCCTTTCAATATTGCTGTTAAGTTTGTTTATAAAACCCTCCACCCTCTCTCC TCAATCCCCCACCTCCTTTCAATATTGCTGTT__GTTTGTTTATAAAACCCTCCACCCTCTCTCC CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28538738..28538823 26863196 MeRIP-seq:(Medium) rs905945541 Functional Loss DEL dbSNP153 33..34 33 - - - 64079 RMVar_ID_64079 Human_SNP_ID_7557492 m1A Human chr1 - 28553139 28553139 28553139 TGTCTTCAGACCCCGGACGGCTGCCCTCACTCACGTCGCCCATCCACAGGCTGGCCGCCATACCC TGTCTTCAGACCCCGGACGGCTGCCCTCACTCGCGTCGCCCATCCACAGGCTGGCCGCCATACCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:28553101..28553282;chr1:28553129..28553511;chr1:28553126..28553272;chr1:28553110..28553396 26863196 MeRIP-seq:(Medium) rs1282739019 Functional Loss SNV dbSNP153 33..33 33 - - - 64080 RMVar_ID_64080 Human_SNP_ID_7565779 m1A Human chr1 + 28581815 28581815 28581815 GCAGCAGCGACTAGCGGGGAACGGCGCGCAGGAAGGCAGGCAGAGGCTTGCAGCTAGTAAGTCGA GCAGCAGCGACTAGCGGGGAACGGCGCGCAGGGAGGCAGGCAGAGGCTTGCAGCTAGTAAGTCGA A G lnc-TRNAU1AP-1 RNACentral:URS00008C385B lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28581759..28581875 26863196 MeRIP-seq:(Medium) rs915823709 Functional Loss SNV dbSNP153 33..33 33 - - - 64081 RMVar_ID_64081 Human_SNP_ID_7565780 m1A Human chr1 + 28581816 28581816 28581816 CAGCAGCGACTAGCGGGGAACGGCGCGCAGGAAGGCAGGCAGAGGCTTGCAGCTAGTAAGTCGAC CAGCAGCGACTAGCGGGGAACGGCGCGCAGGACGGCAGGCAGAGGCTTGCAGCTAGTAAGTCGAC A C lnc-TRNAU1AP-1 RNACentral:URS00008C385B lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28581677..28581875 26863196 MeRIP-seq:(Medium) rs1431145287 Functional Loss SNV dbSNP153 33..33 33 - - - 64082 RMVar_ID_64082 Human_SNP_ID_7568633 m1A Human chr1 - 28592708 28592708 28592708 AGCGCTCGTGGCCCGCGGTGTCCCAGAGTTGCAGCTTGACCCGCGGCCCGGCCCGCAGCTGCAGC AGCGCTCGTGGCCCGCGGTGTCCCAGAGTTGCGGCTTGACCCGCGGCCCGGCCCGCAGCTGCAGC T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28592483..28593744 26863196 MeRIP-seq:(Medium) rs967793770 Functional Loss SNV dbSNP153 33..33 33 - - - 64083 RMVar_ID_64083 Human_SNP_ID_7569008 m1A Human chr1 + 28593972 28593972 28593972 TAAAAACAACTGCAATGTGGACCTGGCCTTTGACACCCTCGCTGATGCTATCCAGCAGGCCCTGC TAAAAACAACTGCAATGTGGACCTGGCCTTTGGCACCCTCGCTGATGCTATCCAGCAGGCCCTGC A G RAB42 Ensembl:ENSG00000188060 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28593922..28594196 26863196 MeRIP-seq:(Medium) rs1251505978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27397275 64084 RMVar_ID_64084 Human_SNP_ID_7575697 m1A Human chr1 - 28622009 28622009 28622009 ATTTCTCATCCATAAAACCGGAACCAGCCAGCACCCCTCCACAAGGCTCCATGGCCAATAGTACT ATTTCTCATCCATAAAACCGGAACCAGCCAGCGCCCCTCCACAAGGCTCCATGGCCAATAGTACT T C TAF12 Ensembl:ENSG00000120656 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28621960..28622160 26863196 MeRIP-seq:(Medium) rs1312407716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351305,Human_RBP_ID_17220997,Human_RBP_ID_17338068,Human_RBP_ID_19335388,Human_RBP_ID_26798003 Human_Splice_Rec_37889,Human_Splice_Rec_37899,Human_Splice_Rec_37911 RMVar_hsa_circ_284534,RMVar_hsa_circ_276905,RMVar_hsa_circ_130884,RMVar_hsa_circ_130885,RMVar_hsa_circ_284348,RMVar_hsa_circ_130887,RMVar_hsa_circ_348342 64085 RMVar_ID_64085 Human_SNP_ID_7581529 m1A Human chr1 - 28642826 28642826 28642826 GGGACTGACTGAGAGGATCAGGCTCGGAGAAGACGCGGCTGTGGGGACCCGGGCTCTAAGACGGG GGGACTGACTGAGAGGATCAGGCTCGGAGAAGGCGCGGCTGTGGGGACCCGGGCTCTAAGACGGG T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:28642809..28643054 26863196 MeRIP-seq:(Medium) rs1557478020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10918958 64086 RMVar_ID_64086 Human_SNP_ID_7581583 m1A Human chr1 + 28643035 28643035 28643035 TCTATCTCCCCATGATATGCAGAGACTGCCCCAGTGAAGCGTTCGTCTCAGCAGCCGGTCCGACT TCTATCTCCCCATGATATGCAGAGACTGCCCCCGTGAAGCGTTCGTCTCAGCAGCCGGTCCGACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28642481..28643047 26863196 MeRIP-seq:(Medium) rs1176151469 Functional Loss SNV dbSNP153 33..33 33 - - - 64087 RMVar_ID_64087 Human_SNP_ID_7583283 m1A Human chr1 - 28648649 28648649 28648649 TTCCGAAATCTCTTGATGTCGATTCCGCACGCAGAGCAATCGAGTTGCCCTACGTGTGCCACTCA TTCCGAAATCTCTTGATGTCGATTCCGCACGCCGAGCAATCGAGTTGCCCTACGTGTGCCACTCA T G SNHG12 RNACentral:URS00007B872B lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:28648605..28648701 26863410 MeRIP-seq:(Medium) rs923725913 Functional Loss SNV dbSNP153 33..33 33 - - - 64088 RMVar_ID_64088 Human_SNP_ID_7583324 m1A Human chr1 + 28648669 28648667 28648669 ACTCGATTGCTCTGCGTGCGGAATCGACATCAAGAGATTTCGGAAGCATAATTTTTTGGTATTTG ACTCGATTGCTCTGCGTGCGGAATCGACATC__GAGATTTCGGAAGCATAATTTTTTGGTATTTG CAA C SNHG12 RNACentral:URS00007B872B lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1557481590 Functional Loss DEL dbSNP153 32..33 33 - - - 64089 RMVar_ID_64089 Human_SNP_ID_7583328 m1A Human chr1 + 28648669 28648669 28648669 ACTCGATTGCTCTGCGTGCGGAATCGACATCAAGAGATTTCGGAAGCATAATTTTTTGGTATTTG ACTCGATTGCTCTGCGTGCGGAATCGACATCACGAGATTTCGGAAGCATAATTTTTTGGTATTTG A C SNHG12 RNACentral:URS00007B872B lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs374428267 Functional Loss SNV dbSNP153 33..33 33 - - - 64090 RMVar_ID_64090 Human_SNP_ID_7583329 m1A Human chr1 + 28648669 28648669 28648669 ACTCGATTGCTCTGCGTGCGGAATCGACATCAAGAGATTTCGGAAGCATAATTTTTTGGTATTTG ACTCGATTGCTCTGCGTGCGGAATCGACATCAGGAGATTTCGGAAGCATAATTTTTTGGTATTTG A G SNHG12 RNACentral:URS00007B872B lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs374428267 Functional Loss SNV dbSNP153 33..33 33 - - - 64091 RMVar_ID_64091 Human_SNP_ID_7589099 m1A Human chr1 - 28668841 28668841 28668841 CCGCGCCCGCGCGCCCACCCCTCCCCCTCCTCACCGTCTCCGTCGGGCGGGCGGGCGGCGAGCGG CCGCGCCCGCGCGCCCACCCCTCCCCCTCCTCCCCGTCTCCGTCGGGCGGGCGGGCGGCGAGCGG T G SNHG12 RNACentral:URS00007B872B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28668808..28668883 26863196 MeRIP-seq:(Medium) rs1371996500 Functional Loss SNV dbSNP153 33..33 33 - - - 64092 RMVar_ID_64092 Human_SNP_ID_7589207 m1A Human chr1 - 28669042 28669042 28669042 GGCTCGGGCGGACCCAGCGGCAGCGTCCCCCCACCCCCCCGCGGCGCCGCGACGTCCGCTCGCTC GGCTCGGGCGGACCCAGCGGCAGCGTCCCCCCCCCCCCCCGCGGCGCCGCGACGTCCGCTCGCTC T G SNHG12 RNACentral:URS00007B872B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:28669031..28669187 26863196 MeRIP-seq:(Medium) rs956412493 Functional Loss SNV dbSNP153 33..33 33 - - - 64093 RMVar_ID_64093 Human_SNP_ID_7607873 m1A Human chr1 + 28737266 28737266 28737266 GAGCCGAGCCGAGGCGTCGTCTCTTGCGGGCCAGGTTTCGGGCCTCTCAGGCCGGCCGCGCCCGG GAGCCGAGCCGAGGCGTCGTCTCTTGCGGGCCGGGTTTCGGGCCTCTCAGGCCGGCCGCGCCCGG A G YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28737259..28737660 26863196 MeRIP-seq:(Medium) rs971001954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351334,Human_RBP_ID_1428566,Human_RBP_ID_22140952 RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 64094 RMVar_ID_64094 Human_SNP_ID_7609631 m1A Human chr1 + 28742517 28742517 28742517 AAGCTGCTTGGTCTACGGGGGGTGACACAGCCATGCCCTACTTAACTTCTTATGGACAGCTGAGC AAGCTGCTTGGTCTACGGGGGGTGACACAGCCGTGCCCTACTTAACTTCTTATGGACAGCTGAGC A G YTHDF2 Ensembl:ENSG00000198492 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:28742476..28742578 32194978 MeRIP-seq:(Medium) rs1282382330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1348016,Human_RBP_ID_1428582,Human_RBP_ID_1744714,Human_RBP_ID_5806447,Human_RBP_ID_8747837,Human_RBP_ID_9268532,Human_RBP_ID_10919728,Human_RBP_ID_17217796,Human_RBP_ID_17335138,Human_RBP_ID_17452221,Human_RBP_ID_17748098,Human_RBP_ID_22023067,Human_RBP_ID_22429181,Human_RBP_ID_27397319,Human_RBP_ID_27592887 Human_miRNA_ID_2491938,Human_miRNA_ID_2491939,Human_miRNA_ID_2694864,Human_miRNA_ID_2694865 RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130904,RMVar_hsa_circ_130903,RMVar_hsa_circ_271547 64095 RMVar_ID_64095 Human_SNP_ID_7652784 m1A Human chr1 + 28914595 28914595 28914595 CCTCGCAGAGGGAAGGCGGGAGGGCGCGCGCCAGGGTCGCTCGCTCGCTCCCTCCCTCCGCTGGT CCTCGCAGAGGGAAGGCGGGAGGGCGCGCGCCGGGGTCGCTCGCTCGCTCCCTCCCTCCGCTGGT A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28914583..28914804 26863196 MeRIP-seq:(Medium) rs913279311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4043376,Human_RBP_ID_5273420,Human_RBP_ID_18473866 Human_miRNA_ID_2688421 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905 64096 RMVar_ID_64096 Human_SNP_ID_7652845 m1A Human chr1 + 28914761 28914761 28914761 CAGCAGTGGCGGGCGCAGGAGCCCGGCCCCGGAGCCACCGGTGAGGCGAGGCGGCGGCGGCGGCG CAGCAGTGGCGGGCGCAGGAGCCCGGCCCCGGGGCCACCGGTGAGGCGAGGCGGCGGCGGCGGCG A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:28914586..28914827 26863196 MeRIP-seq:(Medium) rs1331610678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222530 Human_Splice_Rec_38601,Human_Splice_Rec_38635,Human_Splice_Rec_38663,Human_Splice_Rec_38717,Human_Splice_Rec_38749,Human_Splice_Rec_38781,Human_Splice_Rec_38813,Human_Splice_Rec_38847,Human_Splice_Rec_38875,Human_Splice_Rec_38913 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905 64097 RMVar_ID_64097 Human_SNP_ID_7652924 m1A Human chr1 + 28914965 28914965 28914965 GCACGCCGAGTCGCCAGCCGGGACGCGGCCCGAGGAGCGAGGGGCGGGCCAGAGCCGCTGAGGAA GCACGCCGAGTCGCCAGCCGGGACGCGGCCCGTGGAGCGAGGGGCGGGCCAGAGCCGCTGAGGAA A T EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28914962..28915067 26863196 MeRIP-seq:(Medium) rs1010220844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22562711 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905 64098 RMVar_ID_64098 Human_SNP_ID_7663195 m1A Human chr1 + 28959049 28959049 28959049 GAGATGCAGGCTTGGGGTATTATAAAGAAGGCAGATGCAGGGAAGTGCAGGCTGTTTTAGGAAGC GAGATGCAGGCTTGGGGTATTATAAAGAAGGCGGATGCAGGGAAGTGCAGGCTGTTTTAGGAAGC A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:28959048..28959138 26863196 MeRIP-seq:(Medium) rs1162731005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905 64099 RMVar_ID_64099 Human_SNP_ID_7668742 m1A Human chr1 - 28982626 28982626 28982626 AAAACCATGATGGGCTTTTTGCTGTAGGCCCGAGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA AAAACCATGATGGGCTTTTTGCTGTAGGCCCGTGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA T A RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112223317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4093723,Human_RBP_ID_5156043,Human_RBP_ID_8307589,Human_RBP_ID_17181864,Human_RBP_ID_22141004,Human_RBP_ID_24397143,Human_RBP_ID_24452000,Human_RBP_ID_26390815,Human_RBP_ID_26861441 64100 RMVar_ID_64100 Human_SNP_ID_7668743 m1A Human chr1 - 28982626 28982626 28982626 AAAACCATGATGGGCTTTTTGCTGTAGGCCCGAGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA AAAACCATGATGGGCTTTTTGCTGTAGGCCCGGGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112223317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4093723,Human_RBP_ID_5156043,Human_RBP_ID_8307589,Human_RBP_ID_17181864,Human_RBP_ID_22141004,Human_RBP_ID_24397143,Human_RBP_ID_24452000,Human_RBP_ID_26390815,Human_RBP_ID_26861441 64101 RMVar_ID_64101 Human_SNP_ID_7700730 m1A Human chr1 + 29121319 29121319 29121319 ACGGCTCGGGGACTCCTAGGGCCGGGGCTGGGAAGGAGGGCGCAGTCCCAGCCCGGGCCGTCGGG ACGGCTCGGGGACTCCTAGGGCCGGGGCTGGGGAGGAGGGCGCAGTCCCAGCCCGGGCCGTCGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:29121269..29121618 32194978 MeRIP-seq:(Medium) rs1007796623 Functional Loss SNV dbSNP153 33..33 33 - - - 64102 RMVar_ID_64102 Human_SNP_ID_7708575 m1A Human chr1 - 29148100 29148100 29148100 CCTACAGGGAGCTCAGTAACCTGGACGGCTCTAAGGCTGGAATGACCACATAGGTAGGTATGGTG CCTACAGGGAGCTCAGTAACCTGGACGGCTCTGAGGCTGGAATGACCACATAGGTAGGTATGGTG T C SRSF4 Ensembl:ENSG00000116350 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:29148049..29148311 26863196 MeRIP-seq:(Medium) rs1558384900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273421,Human_RBP_ID_351470,Human_RBP_ID_977490,Human_RBP_ID_1428644,Human_RBP_ID_1744816,Human_RBP_ID_3309344,Human_RBP_ID_5807172,Human_RBP_ID_8968593,Human_RBP_ID_10922729,Human_RBP_ID_17217830,Human_RBP_ID_17335169,Human_RBP_ID_17452266,Human_RBP_ID_17748203,Human_RBP_ID_18228932,Human_RBP_ID_18571372,Human_RBP_ID_22020195,Human_RBP_ID_26310690 RMVar_hsa_circ_130936,RMVar_hsa_circ_130937,RMVar_hsa_circ_130935 64103 RMVar_ID_64103 Human_SNP_ID_7708878 m1A Human chr1 - 29148892 29148868 29148892 AGAAGAGCCTCCGCCAGAGTCGGAGCCGGAGCAGGAGCAAAGGGGGCAGCAGGAGCCGGAGCAGG AGAAGAGCCTCCGCCAGAGTCGGAGCCGGAGC________________________CGGAGCAGG GGCTCCTGCTGCCCCCTTTGCTCCT G SRSF4 Ensembl:ENSG00000116350 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:29148701..29149025 26863196 MeRIP-seq:(Medium) rs1173440023 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_5518747,Human_RBP_ID_5807194,Human_RBP_ID_24541052,Human_RBP_ID_24550343,Human_RBP_ID_26310698,Human_RBP_ID_26378797,Human_RBP_ID_27797693 RMVar_hsa_circ_130936,RMVar_hsa_circ_130937,RMVar_hsa_circ_130935 64104 RMVar_ID_64104 Human_SNP_ID_7708884 m1A Human chr1 - 29148877 29148877 29148877 AGAGTCGGAGCCGGAGCAGGAGCAAAGGGGGCAGCAGGAGCCGGAGCAGGAGCCGCAGCAAGAGC AGAGTCGGAGCCGGAGCAGGAGCAAAGGGGGCGGCAGGAGCCGGAGCAGGAGCCGCAGCAAGAGC T C SRSF4 Ensembl:ENSG00000116350 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:29148730..29149014 26863196 MeRIP-seq:(Medium) rs1303983815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518747,Human_RBP_ID_24541052,Human_RBP_ID_24550343,Human_RBP_ID_24681601,Human_RBP_ID_26310697,Human_RBP_ID_26378797,Human_RBP_ID_27797692 RMVar_hsa_circ_130936,RMVar_hsa_circ_130937,RMVar_hsa_circ_130935 64105 RMVar_ID_64105 Human_SNP_ID_7708915 m1A Human chr1 - 29148919 29148919 29148919 GGAGTGTGAGCAGGGGCAGGAGCCAGGAGAAGAGCCTCCGCCAGAGTCGGAGCCGGAGCAGGAGC GGAGTGTGAGCAGGGGCAGGAGCCAGGAGAAGCGCCTCCGCCAGAGTCGGAGCCGGAGCAGGAGC T G SRSF4 Ensembl:ENSG00000116350 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:29148701..29149000 26863196 MeRIP-seq:(Medium) rs777746638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191356,Human_RBP_ID_4043605,Human_RBP_ID_5109055,Human_RBP_ID_5518747,Human_RBP_ID_5807194,Human_RBP_ID_17646319,Human_RBP_ID_24358742,Human_RBP_ID_24541053,Human_RBP_ID_24550343,Human_RBP_ID_26310698,Human_RBP_ID_27797693 RMVar_hsa_circ_130936,RMVar_hsa_circ_130937,RMVar_hsa_circ_130935 64106 RMVar_ID_64106 Human_SNP_ID_7710626 m1A Human chr1 - 29154752 29154752 29154752 GAAGTCAATGGGAGAAAAATCAGATTAGTTGAAGACAAGCCAGGTTCCAGACGACGCCGGTCCTA GAAGTCAATGGGAGAAAAATCAGATTAGTTGAGGACAAGCCAGGTTCCAGACGACGCCGGTCCTA T C SRSF4 Ensembl:ENSG00000116350 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:29154662..29154814 26863196 MeRIP-seq:(Medium) rs751326953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18094,Human_RBP_ID_1428661,Human_RBP_ID_1744826,Human_RBP_ID_5807219,Human_RBP_ID_8307635,Human_RBP_ID_9355886,Human_RBP_ID_10922908,Human_RBP_ID_18571406,Human_RBP_ID_19034416,Human_RBP_ID_22784096,Human_RBP_ID_22861621,Human_RBP_ID_23385843,Human_RBP_ID_24681651,Human_RBP_ID_26309695 Human_Splice_Rec_39149,Human_Splice_Rec_39161,Human_Splice_Rec_39171 Human_miRNA_ID_2722962 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_280671,RMVar_hsa_circ_130938,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941,RMVar_hsa_circ_130939 64107 RMVar_ID_64107 Human_SNP_ID_7710641 m1A Human chr1 + 29154878 29154878 29154878 CCTTCATTTTTGCGTCCCTTGTGAGCATCTGCATAAGTCACTTCTCCTGCCTGACGCATATAATC CCTTCATTTTTGCGTCCCTTGTGAGCATCTGCGTAAGTCACTTCTCCTGCCTGACGCATATAATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:29154676..29159532;chr1:29154641..29159546 26863196 MeRIP-seq:(Medium) rs779179050 Functional Loss SNV dbSNP153 33..33 33 - - - 64108 RMVar_ID_64108 Human_SNP_ID_7717883 m1A Human chr1 + 29181787 29181762 29181787 CGGCAACGGCAGTGATGGCTGGCCCCGGCCCCAGCCCCCCTTAGGCGGCGGCGGGCAAAGCGAGA CGGCAACG_________________________GCCCCCCTTAGGCGGCGGCGGGCAAAGCGAGA GGCAGTGATGGCTGGCCCCGGCCCCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:29181701..29181850 26863410 MeRIP-seq:(Medium) rs1558395899 Functional Loss DEL dbSNP153 9..33 33 - - - 64109 RMVar_ID_64109 Human_SNP_ID_7717887 m1A Human chr1 - 29181774 29181774 29181774 GCCGCCGCCTAAGGGGGGCTGGGGCCGGGGCCAGCCATCACTGCCGTTGCCGGGATGCCGCGGGT GCCGCCGCCTAAGGGGGGCTGGGGCCGGGGCCGGCCATCACTGCCGTTGCCGGGATGCCGCGGGT T C SRSF4 Ensembl:ENSG00000116350 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:29181729..29181859 26863196 MeRIP-seq:(Medium) rs748935710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073788,Human_RBP_ID_9318779,Human_RBP_ID_18473876,Human_RBP_ID_22023086,Human_RBP_ID_22141174,Human_RBP_ID_22531933,Human_RBP_ID_23112651,Human_RBP_ID_23117643,Human_RBP_ID_26310712,Human_RBP_ID_26861706 Human_miRNA_ID_2456091,Human_miRNA_ID_2460999,Human_miRNA_ID_2633657,Human_miRNA_ID_2636344 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 64110 RMVar_ID_64110 Human_SNP_ID_7717909 m1A Human chr1 + 29181830 29181804 29181830 GGCGGCGGCGGGCAAAGCGAGAGCACGGCGGCAGCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA GGCGGCG__________________________GCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA GGCGGGCAAAGCGAGAGCACGGCGGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:29173485..29181941;chr1:29173485..29181937 26863196 MeRIP-seq:(Medium) rs1558395940 Functional Loss DEL dbSNP153 8..33 33 - - - 64111 RMVar_ID_64111 Human_SNP_ID_7717933 m1A Human chr1 + 29181830 29181827 29181830 GGCGGCGGCGGGCAAAGCGAGAGCACGGCGGCAGCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA GGCGGCGGCGGGCAAAGCGAGAGCACGGCG___GCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA GGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:29173485..29181941;chr1:29173485..29181937 26863196 MeRIP-seq:(Medium) rs1233028501 Functional Loss DEL dbSNP153 31..33 33 - - - 64112 RMVar_ID_64112 Human_SNP_ID_7717936 m1A Human chr1 + 29181830 29181830 29181830 GGCGGCGGCGGGCAAAGCGAGAGCACGGCGGCAGCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA GGCGGCGGCGGGCAAAGCGAGAGCACGGCGGCGGCGGCGGCGGCGGCAACGGGCGGGCGGCGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:29173485..29181941;chr1:29173485..29181937 26863196 MeRIP-seq:(Medium) rs932019707 Functional Loss SNV dbSNP153 33..33 33 - - - 64113 RMVar_ID_64113 Human_SNP_ID_7717976 m1A Human chr1 + 29181866 29181866 29181866 GCGGCGGCGGCAACGGGCGGGCGGCGGGACGGACGCAGCCGAACCCCGGCGACGTACGCGAGCAC GCGGCGGCGGCAACGGGCGGGCGGCGGGACGGGCGCAGCCGAACCCCGGCGACGTACGCGAGCAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:29181766..29181898 26863410 MeRIP-seq:(Medium) rs893407516 Functional Loss SNV dbSNP153 33..33 33 - - - 64114 RMVar_ID_64114 Human_SNP_ID_7723161 m1A Human chr1 - 29203187 29203187 29203187 CAGAATGCATCCAACAGCGGAGTGGGGCAAGCAGTCATCCAGATCGCCGCAGCCCTGGGCCTAAG CAGAATGCATCCAACAGCGGAGTGGGGCAAGCGGTCATCCAGATCGCCGCAGCCCTGGGCCTAAG T C MECR Ensembl:ENSG00000116353 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1062924 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_849752,Human_RBP_ID_3935627 Human_Splice_Rec_39206,Human_Splice_Rec_39207,Human_Splice_Rec_39224,Human_Splice_Rec_39225,Human_Splice_Rec_39235,Human_Splice_Rec_39268,Human_Splice_Rec_39269,Human_Splice_Rec_39278,Human_Splice_Rec_39279,Human_Splice_Rec_39296,Human_Splice_Rec_39297,Human_Splice_Rec_39317,Human_Splice_Rec_39344,Human_Splice_Rec_39354 GWAS_ID_7756,GWAS_ID_7757,GWAS_ID_7758,GWAS_ID_7759,GWAS_ID_7760,GWAS_ID_7761,GWAS_ID_7762,GWAS_ID_7763,GWAS_ID_7764,GWAS_ID_7765,GWAS_ID_7766,GWAS_ID_7767,GWAS_ID_7768,GWAS_ID_7769,GWAS_ID_7770,GWAS_ID_7771,GWAS_ID_7772,GWAS_ID_7773,GWAS_ID_7774,GWAS_ID_7775,GWAS_ID_7776,GWAS_ID_7777,GWAS_ID_7778,GWAS_ID_7779,GWAS_ID_7780,GWAS_ID_7781,GWAS_ID_7782,GWAS_ID_7783,GWAS_ID_7784,GWAS_ID_7785,GWAS_ID_7786,GWAS_ID_7787,GWAS_ID_7788,GWAS_ID_7789,GWAS_ID_7790,GWAS_ID_7791,GWAS_ID_7792,GWAS_ID_7793,GWAS_ID_7794,GWAS_ID_7795,GWAS_ID_7796,GWAS_ID_7797,GWAS_ID_7798,GWAS_ID_7799,GWAS_ID_7800,GWAS_ID_7801,GWAS_ID_7802,GWAS_ID_7803,GWAS_ID_7804,GWAS_ID_7805,GWAS_ID_7806,GWAS_ID_7807,GWAS_ID_7808,GWAS_ID_7809,GWAS_ID_7810,GWAS_ID_7811,GWAS_ID_7812,GWAS_ID_7813,GWAS_ID_7814,GWAS_ID_7815,GWAS_ID_7816,GWAS_ID_7817,GWAS_ID_7818,GWAS_ID_7819,GWAS_ID_7820,GWAS_ID_7821,GWAS_ID_7822,GWAS_ID_7823,GWAS_ID_7824,GWAS_ID_7825,GWAS_ID_7826,GWAS_ID_7827,GWAS_ID_7828,GWAS_ID_7829,GWAS_ID_7830,GWAS_ID_7831,GWAS_ID_7832,GWAS_ID_7833,GWAS_ID_7834,GWAS_ID_7835,GWAS_ID_7836,GWAS_ID_7837,GWAS_ID_7838,GWAS_ID_7839,GWAS_ID_7840,GWAS_ID_7841,GWAS_ID_7842,GWAS_ID_7843,GWAS_ID_7844 RMVar_hsa_circ_26754,RMVar_hsa_circ_353558,RMVar_hsa_circ_17719,RMVar_hsa_circ_79279,RMVar_hsa_circ_6218,RMVar_hsa_circ_130945,RMVar_hsa_circ_318371,RMVar_hsa_circ_130947,RMVar_hsa_circ_370288,RMVar_hsa_circ_55808,RMVar_hsa_circ_130948 64115 RMVar_ID_64115 Human_SNP_ID_7729649 m1A Human chr1 + 29230813 29230813 29230813 CCGGGCAGGCTCGGCGGATGCGGAGTAGGAGGAGGCGGCAGGTCCGTGACAGCCAGAAGCTGGGA CCGGGCAGGCTCGGCGGATGCGGAGTAGGAGGCGGCGGCAGGTCCGTGACAGCCAGAAGCTGGGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:29230764..29230893 26863196 MeRIP-seq:(Medium) rs747260338 Functional Loss SNV dbSNP153 33..33 33 - - - 64116 RMVar_ID_64116 Human_SNP_ID_396492034 m1A Human chr9 + 32384675 32384675 32384675 GAGGCGGCAGCTGGAACCGCGCAGCGCACGGGAACGCGTCCCGCTGCTTGGGTCAGGTTCGCCGG GAGGCGGCAGCTGGAACCGCGCAGCGCACGGGGACGCGTCCCGCTGCTTGGGTCAGGTTCGCCGG A G ACO1 Ensembl:ENSG00000122729 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:32384626..32384772 26863196 MeRIP-seq:(Medium) rs1563923974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717364,Human_RBP_ID_5036113,Human_RBP_ID_9314953,Human_RBP_ID_9339426 Human_Splice_Rec_1037081,Human_Splice_Rec_1037123,Human_Splice_Rec_1037165 64117 RMVar_ID_64117 Human_SNP_ID_396508397 m1A Human chr9 + 32451146 32451125 32451146 CCAATTATCTGCTCATTTTTACCCCTGTAGTCATTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC CCAATTATCTGC_____________________TTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC CTCATTTTTACCCCTGTAGTCA C ACO1 Ensembl:ENSG00000122729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1401946223 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_26564989 64118 RMVar_ID_64118 Human_SNP_ID_396508407 m1A Human chr9 + 32451146 32451146 32451146 CCAATTATCTGCTCATTTTTACCCCTGTAGTCATTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC CCAATTATCTGCTCATTTTTACCCCTGTAGTCGTTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC A G ACO1 Ensembl:ENSG00000122729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7042042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26564989 GWAS_ID_7845,GWAS_ID_7846,GWAS_ID_7847,GWAS_ID_7848,GWAS_ID_7849,GWAS_ID_7850,GWAS_ID_7851,GWAS_ID_7852 64119 RMVar_ID_64119 Human_SNP_ID_396534276 m1A Human chr9 + 32552394 32552394 32552394 GCCACCGCCTGGGAGGTTACTGTAAGGCCCGCAGCTCCCGCCAGCTCCCGCGGACTGCTGCCGCC GCCACCGCCTGGGAGGTTACTGTAAGGCCCGCGGCTCCCGCCAGCTCCCGCGGACTGCTGCCGCC A G SMIM27 Ensembl:ENSG00000235453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:32552285..32552514 26863196 MeRIP-seq:(Medium) rs1436648347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717395,Human_RBP_ID_5036115 Human_Splice_Rec_1037279,Human_Splice_Rec_1037283,Human_Splice_Rec_1037285,Human_Splice_Rec_1037287 64120 RMVar_ID_64120 Human_SNP_ID_396534285 m1A Human chr9 - 32552407 32552407 32552407 TTCATGGTAAGGAGGCGGCAGCAGTCCGCGGGAGCTGGCGGGAGCTGCGGGCCTTACAGTAACCT TTCATGGTAAGGAGGCGGCAGCAGTCCGCGGGCGCTGGCGGGAGCTGCGGGCCTTACAGTAACCT T G TOPORS Ensembl:ENSG00000197579 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr9:32552390..32552553;chr9:32552383..32552552 26863410,26863196 MeRIP-seq:(Medium) rs759172519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961998,Human_RBP_ID_19143272 64121 RMVar_ID_64121 Human_SNP_ID_396536039 m1A Human chr9 - 32558929 32558925 32558930 ATTACAGGAAAAACCATATGGCATAGTTGAAAAGAAGTCCAGAATATTCCCTGTAAGTCTTAACA ATTACAGGAAAAACCATATGGCATAGTTGAA_____GTCCAGAATATTCCCTGTAAGTCTTAACA CTTCTT C NDUFB6 Ensembl:ENSG00000165264 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs776508109 Functional Loss DEL dbSNP153 32..36 33 - - - Human_Splice_Rec_1037296,Human_Splice_Rec_1037297,Human_Splice_Rec_1037300,Human_Splice_Rec_1037301 64122 RMVar_ID_64122 Human_SNP_ID_396539003 m1A Human chr9 + 32570053 32570053 32570053 ATGCCTGTATTTGGCCAATCTCCCTATATATAACCCATCTCCTGTCACCACAACCACATCCCAGC ATGCCTGTATTTGGCCAATCTCCCTATATATAGCCCATCTCCTGTCACCACAACCACATCCCAGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:32570051..32570413 26863196 MeRIP-seq:(Medium) rs1010676010 Functional Loss SNV dbSNP153 33..33 33 - - - 64123 RMVar_ID_64123 Human_SNP_ID_396539768 m1A Human chr9 + 32572971 32572971 32572971 CCCATCTTCTGTGGGGGCAGCACCGGCTCCCGAGGGCTCAGCTCCTGGTCCTTCAGCCATCGCCT CCCATCTTCTGTGGGGGCAGCACCGGCTCCCGGGGGCTCAGCTCCTGGTCCTTCAGCCATCGCCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:32572926..32573150 26863196 MeRIP-seq:(Medium) rs770583535 Functional Loss SNV dbSNP153 33..33 33 - - - 64124 RMVar_ID_64124 Human_SNP_ID_396539772 m1A Human chr9 - 32572981 32572981 32572981 AGAGCTGAGAAGGCGATGGCTGAAGGACCAGGAGCTGAGCCCTCGGGAGCCGGTGCTGCCCCCAC AGAGCTGAGAAGGCGATGGCTGAAGGACCAGGTGCTGAGCCCTCGGGAGCCGGTGCTGCCCCCAC T A NDUFB6 Ensembl:ENSG00000165264 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:32553939..32573150 26863410 MeRIP-seq:(Medium) rs1199466960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_185163,Human_RBP_ID_717422,Human_RBP_ID_5036116,Human_RBP_ID_5329890,Human_RBP_ID_9338883,Human_RBP_ID_9341793,Human_RBP_ID_16652625,Human_RBP_ID_22466039,Human_RBP_ID_26360364 64125 RMVar_ID_64125 Human_SNP_ID_396640428 m1A Human chr9 - 32987589 32987589 32987589 ACAGGGCTGGAACCTGGGAGCAACTCTGGCCAATGCTCTGTGCCCCTAAAGAAGGGAAAAGATGC ACAGGGCTGGAACCTGGGAGCAACTCTGGCCAGTGCTCTGTGCCCCTAAAGAAGGGAAAAGATGC T C APTX Ensembl:ENSG00000137074 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:32987563..32987863 32194978 MeRIP-seq:(Medium) rs768716712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717490,Human_RBP_ID_1059031,Human_RBP_ID_1704732,Human_RBP_ID_5025532,Human_RBP_ID_16653265,Human_RBP_ID_26565711 Human_Splice_Rec_1037321,Human_Splice_Rec_1037341,Human_Splice_Rec_1037351,Human_Splice_Rec_1037365,Human_Splice_Rec_1037389,Human_Splice_Rec_1037403,Human_Splice_Rec_1037431,Human_Splice_Rec_1037443,Human_Splice_Rec_1037455,Human_Splice_Rec_1037467,Human_Splice_Rec_1037479,Human_Splice_Rec_1037491,Human_Splice_Rec_1037501,Human_Splice_Rec_1037511,Human_Splice_Rec_1037527,Human_Splice_Rec_1037539,Human_Splice_Rec_1037555,Human_Splice_Rec_1037565,Human_Splice_Rec_1037579,Human_Splice_Rec_1037593,Human_Splice_Rec_1037607,Human_Splice_Rec_1037621,Human_Splice_Rec_1037631,Human_Splice_Rec_1037643,Human_Splice_Rec_1037663,Human_Splice_Rec_1037673,Human_Splice_Rec_1037689,Human_Splice_Rec_1037701,Human_Splice_Rec_1037709,Human_Splice_Rec_1037719,Human_Splice_Rec_1037727,Human_Splice_Rec_1037753,Human_Splice_Rec_1037767,Human_Splice_Rec_1037777,Human_Splice_Rec_1037791,Human_Splice_Rec_1037805,Human_Splice_Rec_1037819,Human_Splice_Rec_1037831,Human_Splice_Rec_1037847,Human_Splice_Rec_1037859,Human_Splice_Rec_1037865,Human_Splice_Rec_1037873,Human_Splice_Rec_1037883,Human_Splice_Rec_1037893,Human_Splice_Rec_1037901,Human_Splice_Rec_1037905,Human_Splice_Rec_1037915 Human_miRNA_ID_1349028,Human_miRNA_ID_1812858 RMVar_hsa_circ_47627,RMVar_hsa_circ_256299,RMVar_hsa_circ_357381,RMVar_hsa_circ_315498,RMVar_hsa_circ_269636,RMVar_hsa_circ_362679,RMVar_hsa_circ_26015,RMVar_hsa_circ_332673,RMVar_hsa_circ_360098,RMVar_hsa_circ_3133,RMVar_hsa_circ_329730,RMVar_hsa_circ_360148 64126 RMVar_ID_64126 Human_SNP_ID_396640452 m1A Human chr9 - 32987668 32987668 32987668 GGAAACACACAGGAAGAGAAAGAGATCAGGCAACAGTGATTCTATAGAAAGGGATGCTGCTCAGG GGAAACACACAGGAAGAGAAAGAGATCAGGCAGCAGTGATTCTATAGAAAGGGATGCTGCTCAGG T C APTX Ensembl:ENSG00000137074 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:32987617..32987750 26863196 MeRIP-seq:(Medium) rs955636981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1704733,Human_RBP_ID_7921010,Human_RBP_ID_16653271 Human_Splice_Rec_1037320,Human_Splice_Rec_1037350,Human_Splice_Rec_1037442,Human_Splice_Rec_1037454,Human_Splice_Rec_1037490,Human_Splice_Rec_1037510,Human_Splice_Rec_1037526,Human_Splice_Rec_1037592,Human_Splice_Rec_1037606,Human_Splice_Rec_1037642,Human_Splice_Rec_1037672,Human_Splice_Rec_1037766,Human_Splice_Rec_1037776,Human_Splice_Rec_1037804,Human_Splice_Rec_1037846,Human_Splice_Rec_1037882,Human_Splice_Rec_1037892 RMVar_hsa_circ_47627,RMVar_hsa_circ_256299,RMVar_hsa_circ_357381,RMVar_hsa_circ_315498,RMVar_hsa_circ_269636,RMVar_hsa_circ_362679,RMVar_hsa_circ_26015,RMVar_hsa_circ_332673,RMVar_hsa_circ_360098,RMVar_hsa_circ_3133,RMVar_hsa_circ_329730,RMVar_hsa_circ_360148 64127 RMVar_ID_64127 Human_SNP_ID_396641096 m1A Human chr9 - 32989840 32989840 32989840 TGGTGAGACAGGACAGCCGGCACCAGCGAATCAGACTTCCACATTTGGAAGCAGTTGTGATTGGG TGGTGAGACAGGACAGCCGGCACCAGCGAATCGGACTTCCACATTTGGAAGCAGTTGTGATTGGG T C APTX Ensembl:ENSG00000137074 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:32988062..32989900 32194978 MeRIP-seq:(Medium) rs572308162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717492,Human_RBP_ID_1704735,Human_RBP_ID_5036120,Human_RBP_ID_7921026,Human_RBP_ID_24299051,Human_RBP_ID_26239256,Human_RBP_ID_27785339 Human_Splice_Rec_1037316,Human_Splice_Rec_1037317,Human_Splice_Rec_1037336,Human_Splice_Rec_1037337,Human_Splice_Rec_1037348,Human_Splice_Rec_1037349,Human_Splice_Rec_1037360,Human_Splice_Rec_1037361,Human_Splice_Rec_1037374,Human_Splice_Rec_1037375,Human_Splice_Rec_1037384,Human_Splice_Rec_1037385,Human_Splice_Rec_1037398,Human_Splice_Rec_1037399,Human_Splice_Rec_1037412,Human_Splice_Rec_1037413,Human_Splice_Rec_1037426,Human_Splice_Rec_1037427,Human_Splice_Rec_1037439,Human_Splice_Rec_1037451,Human_Splice_Rec_1037463,Human_Splice_Rec_1037475,Human_Splice_Rec_1037487,Human_Splice_Rec_1037497,Human_Splice_Rec_1037508,Human_Splice_Rec_1037509,Human_Splice_Rec_1037522,Human_Splice_Rec_1037523,Human_Splice_Rec_1037536,Human_Splice_Rec_1037537,Human_Splice_Rec_1037550,Human_Splice_Rec_1037551,Human_Splice_Rec_1037574,Human_Splice_Rec_1037575,Human_Splice_Rec_1037588,Human_Splice_Rec_1037589,Human_Splice_Rec_1037602,Human_Splice_Rec_1037603,Human_Splice_Rec_1037616,Human_Splice_Rec_1037617,Human_Splice_Rec_1037639,Human_Splice_Rec_1037659,Human_Splice_Rec_1037670,Human_Splice_Rec_1037671,Human_Splice_Rec_1037684,Human_Splice_Rec_1037685,Human_Splice_Rec_1037698,Human_Splice_Rec_1037699,Human_Splice_Rec_1037738,Human_Splice_Rec_1037739,Human_Splice_Rec_1037748,Human_Splice_Rec_1037749,Human_Splice_Rec_1037762,Human_Splice_Rec_1037763,Human_Splice_Rec_1037774,Human_Splice_Rec_1037775,Human_Splice_Rec_1037786,Human_Splice_Rec_1037787,Human_Splice_Rec_1037799,Human_Splice_Rec_1037814,Human_Splice_Rec_1037815,Human_Splice_Rec_1037826,Human_Splice_Rec_1037827,Human_Splice_Rec_1037842,Human_Splice_Rec_1037843,Human_Splice_Rec_1037878,Human_Splice_Rec_1037879,Human_Splice_Rec_1037888,Human_Splice_Rec_1037889,Human_Splice_Rec_1037898,Human_Splice_Rec_1037899,Human_Splice_Rec_1037910,Human_Splice_Rec_1037911,Human_Splice_Rec_1037918,Human_Splice_Rec_1037919,Human_Splice_Rec_1037922 RMVar_hsa_circ_47627,RMVar_hsa_circ_256299,RMVar_hsa_circ_357381,RMVar_hsa_circ_315498,RMVar_hsa_circ_332673,RMVar_hsa_circ_329730,RMVar_hsa_circ_88851,RMVar_hsa_circ_256300 64128 RMVar_ID_64128 Human_SNP_ID_396641097 m1A Human chr9 - 32989840 32989840 32989840 TGGTGAGACAGGACAGCCGGCACCAGCGAATCAGACTTCCACATTTGGAAGCAGTTGTGATTGGG TGGTGAGACAGGACAGCCGGCACCAGCGAATCCGACTTCCACATTTGGAAGCAGTTGTGATTGGG T G APTX Ensembl:ENSG00000137074 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:32988062..32989900 32194978 MeRIP-seq:(Medium) rs572308162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717492,Human_RBP_ID_1704735,Human_RBP_ID_5036120,Human_RBP_ID_7921026,Human_RBP_ID_24299051,Human_RBP_ID_26239256,Human_RBP_ID_27785339 Human_Splice_Rec_1037316,Human_Splice_Rec_1037317,Human_Splice_Rec_1037336,Human_Splice_Rec_1037337,Human_Splice_Rec_1037348,Human_Splice_Rec_1037349,Human_Splice_Rec_1037360,Human_Splice_Rec_1037361,Human_Splice_Rec_1037374,Human_Splice_Rec_1037375,Human_Splice_Rec_1037384,Human_Splice_Rec_1037385,Human_Splice_Rec_1037398,Human_Splice_Rec_1037399,Human_Splice_Rec_1037412,Human_Splice_Rec_1037413,Human_Splice_Rec_1037426,Human_Splice_Rec_1037427,Human_Splice_Rec_1037439,Human_Splice_Rec_1037451,Human_Splice_Rec_1037463,Human_Splice_Rec_1037475,Human_Splice_Rec_1037487,Human_Splice_Rec_1037497,Human_Splice_Rec_1037508,Human_Splice_Rec_1037509,Human_Splice_Rec_1037522,Human_Splice_Rec_1037523,Human_Splice_Rec_1037536,Human_Splice_Rec_1037537,Human_Splice_Rec_1037550,Human_Splice_Rec_1037551,Human_Splice_Rec_1037574,Human_Splice_Rec_1037575,Human_Splice_Rec_1037588,Human_Splice_Rec_1037589,Human_Splice_Rec_1037602,Human_Splice_Rec_1037603,Human_Splice_Rec_1037616,Human_Splice_Rec_1037617,Human_Splice_Rec_1037639,Human_Splice_Rec_1037659,Human_Splice_Rec_1037670,Human_Splice_Rec_1037671,Human_Splice_Rec_1037684,Human_Splice_Rec_1037685,Human_Splice_Rec_1037698,Human_Splice_Rec_1037699,Human_Splice_Rec_1037738,Human_Splice_Rec_1037739,Human_Splice_Rec_1037748,Human_Splice_Rec_1037749,Human_Splice_Rec_1037762,Human_Splice_Rec_1037763,Human_Splice_Rec_1037774,Human_Splice_Rec_1037775,Human_Splice_Rec_1037786,Human_Splice_Rec_1037787,Human_Splice_Rec_1037799,Human_Splice_Rec_1037814,Human_Splice_Rec_1037815,Human_Splice_Rec_1037826,Human_Splice_Rec_1037827,Human_Splice_Rec_1037842,Human_Splice_Rec_1037843,Human_Splice_Rec_1037878,Human_Splice_Rec_1037879,Human_Splice_Rec_1037888,Human_Splice_Rec_1037889,Human_Splice_Rec_1037898,Human_Splice_Rec_1037899,Human_Splice_Rec_1037910,Human_Splice_Rec_1037911,Human_Splice_Rec_1037918,Human_Splice_Rec_1037919,Human_Splice_Rec_1037922 RMVar_hsa_circ_47627,RMVar_hsa_circ_256299,RMVar_hsa_circ_357381,RMVar_hsa_circ_315498,RMVar_hsa_circ_332673,RMVar_hsa_circ_329730,RMVar_hsa_circ_88851,RMVar_hsa_circ_256300 64129 RMVar_ID_64129 Human_SNP_ID_396644205 m1A Human chr9 + 33001493 33001493 33001493 GCGTCATTCAAGGCACATCACTCAAGGGTAGGAGCAGCCTCGGCCGAACGCTCACCCGCGGCATT GCGTCATTCAAGGCACATCACTCAAGGGTAGGGGCAGCCTCGGCCGAACGCTCACCCGCGGCATT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33001490..33001577 26863196 MeRIP-seq:(Medium) rs1212132414 Functional Loss SNV dbSNP153 33..33 33 - - - 64130 RMVar_ID_64130 Human_SNP_ID_396649550 m1A Human chr9 - 33020219 33020219 33020219 AGCCAGGGTAGGAGCAAAATTGGGTGAAGGAAAAGGTGAGTCCAGGTTTGAATGAGTACAACTAC AGCCAGGGTAGGAGCAAAATTGGGTGAAGGAACAGGTGAGTCCAGGTTTGAATGAGTACAACTAC T G APTX Ensembl:ENSG00000137074 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33020143..33020367 26863196 MeRIP-seq:(Medium) rs1047434681 Functional Loss SNV dbSNP153 33..33 33 - - - 64131 RMVar_ID_64131 Human_SNP_ID_396651141 m1A Human chr9 + 33025074 33025074 33025074 TCTCAGGCTCGCTGAGTGGAGAAAAGGGCTCCAGAAGATTCCACGAGCGCCGGGAAGCCGCGCTA TCTCAGGCTCGCTGAGTGGAGAAAAGGGCTCCGGAAGATTCCACGAGCGCCGGGAAGCCGCGCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33025024..33025105 26863196 MeRIP-seq:(Medium) rs1001617208 Functional Loss SNV dbSNP153 33..33 33 - - - 64132 RMVar_ID_64132 Human_SNP_ID_396651287 m1A Human chr9 + 33025300 33025300 33025300 GCCGGGCGGAACTTTCCAGAACGCTCGGTGAGAGGCGGAGGAGCGGTAACTACCCCGGCTGCGCA GCCGGGCGGAACTTTCCAGAACGCTCGGTGAGCGGCGGAGGAGCGGTAACTACCCCGGCTGCGCA A C DNAJA1 Ensembl:ENSG00000086061 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1485543291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797091,Human_RBP_ID_846252,Human_RBP_ID_1059036,Human_RBP_ID_1704759,Human_RBP_ID_5036122,Human_RBP_ID_5516061,Human_RBP_ID_7921376,Human_RBP_ID_8928055,Human_RBP_ID_22466041,Human_RBP_ID_26833166 Human_Splice_Rec_1037927,Human_Splice_Rec_1037943 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301 64133 RMVar_ID_64133 Human_SNP_ID_396651288 m1A Human chr9 + 33025300 33025300 33025300 GCCGGGCGGAACTTTCCAGAACGCTCGGTGAGAGGCGGAGGAGCGGTAACTACCCCGGCTGCGCA GCCGGGCGGAACTTTCCAGAACGCTCGGTGAGGGGCGGAGGAGCGGTAACTACCCCGGCTGCGCA A G DNAJA1 Ensembl:ENSG00000086061 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1485543291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797091,Human_RBP_ID_846252,Human_RBP_ID_1059036,Human_RBP_ID_1704759,Human_RBP_ID_5036122,Human_RBP_ID_5516061,Human_RBP_ID_7921376,Human_RBP_ID_8928055,Human_RBP_ID_22466041,Human_RBP_ID_26833166 Human_Splice_Rec_1037927,Human_Splice_Rec_1037943 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301 64134 RMVar_ID_64134 Human_SNP_ID_396651316 m1A Human chr9 + 33025334 33025334 33025334 GCGGAGGAGCGGTAACTACCCCGGCTGCGCACAGCTCGGCGCTCCTTCCCGCTCCCTCACACACC GCGGAGGAGCGGTAACTACCCCGGCTGCGCACCGCTCGGCGCTCCTTCCCGCTCCCTCACACACC A C DNAJA1 Ensembl:ENSG00000086061 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:33025251..33025429;chr9:33025240..33025446 26863196 MeRIP-seq:(Medium) rs1053765615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717504,Human_RBP_ID_5036122,Human_RBP_ID_5431157,Human_RBP_ID_5454461,Human_RBP_ID_5482043,Human_RBP_ID_5516062,Human_RBP_ID_7957198,Human_RBP_ID_8928056,Human_RBP_ID_9338884,Human_RBP_ID_22466041,Human_RBP_ID_26833168,Human_RBP_ID_27545452 Human_Splice_Rec_1037927,Human_Splice_Rec_1037943 Human_miRNA_ID_2442924 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301 64135 RMVar_ID_64135 Human_SNP_ID_396651317 m1A Human chr9 + 33025334 33025334 33025334 GCGGAGGAGCGGTAACTACCCCGGCTGCGCACAGCTCGGCGCTCCTTCCCGCTCCCTCACACACC GCGGAGGAGCGGTAACTACCCCGGCTGCGCACGGCTCGGCGCTCCTTCCCGCTCCCTCACACACC A G DNAJA1 Ensembl:ENSG00000086061 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:33025251..33025429;chr9:33025240..33025446 26863196 MeRIP-seq:(Medium) rs1053765615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717504,Human_RBP_ID_5036122,Human_RBP_ID_5431157,Human_RBP_ID_5454461,Human_RBP_ID_5482043,Human_RBP_ID_5516062,Human_RBP_ID_7957198,Human_RBP_ID_8928056,Human_RBP_ID_9338884,Human_RBP_ID_22466041,Human_RBP_ID_26833168,Human_RBP_ID_27545452 Human_Splice_Rec_1037927,Human_Splice_Rec_1037943 Human_miRNA_ID_2442924 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301 64136 RMVar_ID_64136 Human_SNP_ID_396655812 m1A Human chr9 + 33038864 33038862 33038865 CACTACAATGGAGAAGCATATGAGGATGATGAACATCATCCCAGAGGTGGTGTTCAGTGTCAGAC CACTACAATGGAGAAGCATATGAGGATGATG___ATCATCCCAGAGGTGGTGTTCAGTGTCAGAC GAAC G DNAJA1 Ensembl:ENSG00000086061 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:33038814..33038915 32194978 MeRIP-seq:(Medium) rs754394456 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_717514,Human_RBP_ID_9407972,Human_RBP_ID_18134917,Human_RBP_ID_27374564 Human_miRNA_ID_2424147,Human_miRNA_ID_2433807 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301,RMVar_hsa_circ_107549,RMVar_hsa_circ_256305,RMVar_hsa_circ_79715,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_122757,RMVar_hsa_circ_256310,RMVar_hsa_circ_256311 64137 RMVar_ID_64137 Human_SNP_ID_396655813 m1A Human chr9 + 33038864 33038864 33038864 CACTACAATGGAGAAGCATATGAGGATGATGAACATCATCCCAGAGGTGGTGTTCAGTGTCAGAC CACTACAATGGAGAAGCATATGAGGATGATGATCATCATCCCAGAGGTGGTGTTCAGTGTCAGAC A T DNAJA1 Ensembl:ENSG00000086061 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:33038814..33038915 32194978 MeRIP-seq:(Medium) rs1438297754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717514,Human_RBP_ID_9407972,Human_RBP_ID_18134917,Human_RBP_ID_27374564 Human_miRNA_ID_2424147,Human_miRNA_ID_2433807 RMVar_hsa_circ_86836,RMVar_hsa_circ_256301,RMVar_hsa_circ_107549,RMVar_hsa_circ_256305,RMVar_hsa_circ_79715,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_122757,RMVar_hsa_circ_256310,RMVar_hsa_circ_256311 64138 RMVar_ID_64138 Human_SNP_ID_396665538 m1A Human chr9 + 33076636 33076636 33076636 GACATAGCCGTATCTCTCCGGGAGCAGGCCCCAGCTCTCCCTCAAGGCCAGTCGCGCAACACACC GACATAGCCGTATCTCTCCGGGAGCAGGCCCCGGCTCTCCCTCAAGGCCAGTCGCGCAACACACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:33076530..33076675;chr9:33076529..33076675;chr9:33076555..33076700 26863196 MeRIP-seq:(Medium) rs771644843 Functional Loss SNV dbSNP153 33..33 33 - - - 64139 RMVar_ID_64139 Human_SNP_ID_396674808 m1A Human chr9 - 33111953 33111953 33111953 TTTAATTAGTGATCTAGAAAGAAGTTCAGCCGAACCCACACCCCAACTCCCTCCCAAGAACTTCG TTTAATTAGTGATCTAGAAAGAAGTTCAGCCGGACCCACACCCCAACTCCCTCCCAAGAACTTCG T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33111903..33112013 26863196 MeRIP-seq:(Medium) rs944368064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224500,Human_RBP_ID_8952313,Human_RBP_ID_16763843,Human_RBP_ID_22411548,Human_RBP_ID_24299401,Human_RBP_ID_24523378,Human_RBP_ID_26565001 RMVar_hsa_circ_82553,RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_105296,RMVar_hsa_circ_91506,RMVar_hsa_circ_256328,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256329 64140 RMVar_ID_64140 Human_SNP_ID_396674814 m1A Human chr9 + 33111971 33111971 33111971 GTTGGGGTGTGGGTTCGGCTGAACTTCTTTCTAGATCACTAATTAAAAGGCACATTCATGCTGGG GTTGGGGTGTGGGTTCGGCTGAACTTCTTTCTCGATCACTAATTAAAAGGCACATTCATGCTGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33111921..33112014 26863196 MeRIP-seq:(Medium) rs1385247082 Functional Loss SNV dbSNP153 33..33 33 - - - 64141 RMVar_ID_64141 Human_SNP_ID_396674888 m1A Human chr9 + 33112264 33112264 33112264 GCTGGTAAACAACCTGACTGCTGTTATTTACAACCCCCCAGCCTAGGGGCCTGAGGGGTCAGTCT GCTGGTAAACAACCTGACTGCTGTTATTTACAGCCCCCCAGCCTAGGGGCCTGAGGGGTCAGTCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:33112213..33112461 32194978 MeRIP-seq:(Medium) rs1564034186 Functional Loss SNV dbSNP153 33..33 33 - - - 64142 RMVar_ID_64142 Human_SNP_ID_396686778 m1A Human chr9 - 33158323 33158323 33158323 TGCAGAGAGGGATTTCTTGGTCTGCAGAGGGTAGGAGCAAGCCTTGAAGGCTGCTGGAGTGAGGA TGCAGAGAGGGATTTCTTGGTCTGCAGAGGGTCGGAGCAAGCCTTGAAGGCTGCTGGAGTGAGGA T G B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33158320..33158494 26863196 MeRIP-seq:(Medium) rs755627625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3210881,Human_RBP_ID_7921850 RMVar_hsa_circ_97414,RMVar_hsa_circ_256332 64143 RMVar_ID_64143 Human_SNP_ID_396688824 m1A Human chr9 + 33166846 33166846 33166846 ACTGGGACCGAGGTCAAGTTGCTAGCGGGGCCAGGGCCAGAATCCACGACTGGGCTGGAGTCGCC ACTGGGACCGAGGTCAAGTTGCTAGCGGGGCCGGGGCCAGAATCCACGACTGGGCTGGAGTCGCC A G B4GALT1-AS1 RNACentral:URS0000D56DC9 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:33166826..33166850 26863196 MeRIP-seq:(Medium) rs1230727496 Functional Loss SNV dbSNP153 33..33 33 - - - 64144 RMVar_ID_64144 Human_SNP_ID_396688853 m1A Human chr9 + 33166912 33166912 33166912 CCCGGGCGCGGCTGGGAGGAGGCGCCTAGAGGAGGCGGCGGCCGGGCCCCTCCGGTCCGGAGCTC CCCGGGCGCGGCTGGGAGGAGGCGCCTAGAGGCGGCGGCGGCCGGGCCCCTCCGGTCCGGAGCTC A C B4GALT1-AS1 RNACentral:URS0000D56DC9 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:33166872..33167250 26863196 MeRIP-seq:(Medium) rs755473720 Functional Loss SNV dbSNP153 33..33 33 - - - 64145 RMVar_ID_64145 Human_SNP_ID_396712154 m1A Human chr9 - 33259003 33259000 33259003 AGAACAGTCCACAGGAAGAGGTTGAACTAAAGAAGTTGAAACATTTGGAGAAGTCTGTGGAGAAG AGAACAGTCCACAGGAAGAGGTTGAACTAAAG___TTGAAACATTTGGAGAAGTCTGTGGAGAAG ACTT A BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33258895..33259064 26863196 MeRIP-seq:(Medium) rs1176431196 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_92334,Human_RBP_ID_963080,Human_RBP_ID_1704829,Human_RBP_ID_2063887,Human_RBP_ID_3210967,Human_RBP_ID_8703441,Human_RBP_ID_9351877,Human_RBP_ID_9406844,Human_RBP_ID_18135038,Human_RBP_ID_18453494,Human_RBP_ID_26360626,Human_RBP_ID_27832317 Human_Splice_Rec_1038034,Human_Splice_Rec_1038035,Human_Splice_Rec_1038041,Human_Splice_Rec_1038048,Human_Splice_Rec_1038049,Human_Splice_Rec_1038060,Human_Splice_Rec_1038061,Human_Splice_Rec_1038074,Human_Splice_Rec_1038075,Human_Splice_Rec_1038084,Human_Splice_Rec_1038085,Human_Splice_Rec_1038092 RMVar_hsa_circ_57336,RMVar_hsa_circ_312814,RMVar_hsa_circ_347903,RMVar_hsa_circ_306598 64146 RMVar_ID_64146 Human_SNP_ID_396712637 m1A Human chr9 + 33261137 33261137 33261137 GACCCGGCAACCATCTTGTATTCCAAGTGCTGACAACGGTGTTTCCATTTCCTTCAGAGATTTTC GACCCGGCAACCATCTTGTATTCCAAGTGCTGGCAACGGTGTTTCCATTTCCTTCAGAGATTTTC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33261040..33261154 26863196 MeRIP-seq:(Medium) rs1379299992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256334 64147 RMVar_ID_64147 Human_SNP_ID_396713111 m1A Human chr9 + 33262826 33262826 33262826 TGCTGGGAGGTAACATGAAGGTCGTGCTTCTCATTGCCTGGGGAGAAAGAAAAGCATTTGACGAA TGCTGGGAGGTAACATGAAGGTCGTGCTTCTCCTTGCCTGGGGAGAAAGAAAAGCATTTGACGAA A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:33262801..33262825 26863196 MeRIP-seq:(Medium) rs779910385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256334 64148 RMVar_ID_64148 Human_SNP_ID_396713112 m1A Human chr9 + 33262826 33262826 33262826 TGCTGGGAGGTAACATGAAGGTCGTGCTTCTCATTGCCTGGGGAGAAAGAAAAGCATTTGACGAA TGCTGGGAGGTAACATGAAGGTCGTGCTTCTCGTTGCCTGGGGAGAAAGAAAAGCATTTGACGAA A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:33262801..33262825 26863196 MeRIP-seq:(Medium) rs779910385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256334 64149 RMVar_ID_64149 Human_SNP_ID_396713113 m1A Human chr9 - 33262827 33262827 33262827 ATTCGTCAAATGCTTTTCTTTCTCCCCAGGCAATGAGAAGCACGACCTTCATGTTACCTCCCAGC ATTCGTCAAATGCTTTTCTTTCTCCCCAGGCAGTGAGAAGCACGACCTTCATGTTACCTCCCAGC T C BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33262776..33262850 26863196 MeRIP-seq:(Medium) rs1421388081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92340,Human_RBP_ID_9406846 Human_Splice_Rec_1038030,Human_Splice_Rec_1038056,Human_Splice_Rec_1038068,Human_Splice_Rec_1038088,Human_Splice_Rec_1038094,Human_Splice_Rec_1038098 RMVar_hsa_circ_312814,RMVar_hsa_circ_306598 64150 RMVar_ID_64150 Human_SNP_ID_396713520 m1A Human chr9 - 33264290 33264290 33264290 GGAGCCAGGAGGTGACCCGGGACGAGGAGTCGACCCGGAGCGAGGAGGTGACCAGGGAGGAAATG GGAGCCAGGAGGTGACCCGGGACGAGGAGTCGGCCCGGAGCGAGGAGGTGACCAGGGAGGAAATG T C BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33264188..33264750 26863196 MeRIP-seq:(Medium) rs1480104296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963081,Human_RBP_ID_5036694,Human_RBP_ID_8703450,Human_RBP_ID_9406847,Human_RBP_ID_26565008,Human_RBP_ID_27832318 Human_Splice_Rec_1038029,Human_Splice_Rec_1038055,Human_Splice_Rec_1038067,Human_Splice_Rec_1038087,Human_Splice_Rec_1038093,Human_Splice_Rec_1038097 RMVar_hsa_circ_256335 64151 RMVar_ID_64151 Human_SNP_ID_396713560 m1A Human chr9 - 33264367 33264367 33264367 GACCCTGAGTGAGGAAGCGACCTGGAGTGAAGAGGCGACCCAGAGTGAGGAGGCGACCCAGGGCG GACCCTGAGTGAGGAAGCGACCTGGAGTGAAGGGGCGACCCAGAGTGAGGAGGCGACCCAGGGCG T C BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:33264201..33264700 26863196 MeRIP-seq:(Medium) rs765379810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9406848,Human_RBP_ID_24299504,Human_RBP_ID_26565008,Human_RBP_ID_27832318 Human_Splice_Rec_1038097 RMVar_hsa_circ_256335 64152 RMVar_ID_64152 Human_SNP_ID_396713561 m1A Human chr9 - 33264367 33264367 33264367 GACCCTGAGTGAGGAAGCGACCTGGAGTGAAGAGGCGACCCAGAGTGAGGAGGCGACCCAGGGCG GACCCTGAGTGAGGAAGCGACCTGGAGTGAAGCGGCGACCCAGAGTGAGGAGGCGACCCAGGGCG T G BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:33264201..33264700 26863196 MeRIP-seq:(Medium) rs765379810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9406848,Human_RBP_ID_24299504,Human_RBP_ID_26565008,Human_RBP_ID_27832318 Human_Splice_Rec_1038097 RMVar_hsa_circ_256335 64153 RMVar_ID_64153 Human_SNP_ID_396713565 m1A Human chr9 - 33264380 33264380 33264380 GGAGCGAGGAGTTGACCCTGAGTGAGGAAGCGACCTGGAGTGAAGAGGCGACCCAGAGTGAGGAG GGAGCGAGGAGTTGACCCTGAGTGAGGAAGCGTCCTGGAGTGAAGAGGCGACCCAGAGTGAGGAG T A BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33264195..33264750 26863196 MeRIP-seq:(Medium) rs1405676120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717745,Human_RBP_ID_9406848,Human_RBP_ID_16656315,Human_RBP_ID_24299504,Human_RBP_ID_26565008,Human_RBP_ID_27832318 RMVar_hsa_circ_256335 64154 RMVar_ID_64154 Human_SNP_ID_396716538 m1A Human chr9 - 33276406 33276406 33276406 AGAGGATTTTCTCTCATTTACCATTTTCTTTTAACTACCCTTTTCCCCTACATTCTCCTTTGAAT AGAGGATTTTCTCTCATTTACCATTTTCTTTTGACTACCCTTTTCCCCTACATTCTCCTTTGAAT T C RF00017-4575,lnc-BAG1-2 RNACentral:URS0000918622,RNACentral:URS00008C194B SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33276403..33276476 26863196 MeRIP-seq:(Medium) rs1299114541 Functional Loss SNV dbSNP153 33..33 33 - - - 64155 RMVar_ID_64155 Human_SNP_ID_396716807 m1A Human chr9 + 33277415 33277415 33277415 TAGGGAAGAAGTATGGGGTAGCATGGGAGCACATACTAAGGGACTCTAACCTAGTTAGTAGTGGG TAGGGAAGAAGTATGGGGTAGCATGGGAGCACGTACTAAGGGACTCTAACCTAGTTAGTAGTGGG A G CHMP5 Ensembl:ENSG00000086065 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33277409..33277682 26863196 MeRIP-seq:(Medium) rs912444871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10428618 RMVar_hsa_circ_256337,RMVar_hsa_circ_256336,RMVar_hsa_circ_119806,RMVar_hsa_circ_273557,RMVar_hsa_circ_256339,RMVar_hsa_circ_281072,RMVar_hsa_circ_298391 64156 RMVar_ID_64156 Human_SNP_ID_396717711 m1A Human chr9 + 33281356 33281356 33281356 TTGTGTCTTGTGAACAAGTCGTTACTGTGTCCATTATTGGAATGGAATTATCACTACTGTATCAT TTGTGTCTTGTGAACAAGTCGTTACTGTGTCCGTTATTGGAATGGAATTATCACTACTGTATCAT A G CHMP5 Ensembl:ENSG00000086065 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:33281172..33281422 32194978 MeRIP-seq:(Medium) rs1251747744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717764,Human_RBP_ID_1704835,Human_RBP_ID_3899020,Human_RBP_ID_5123885,Human_RBP_ID_8703460,Human_RBP_ID_8952321,Human_RBP_ID_23216433,Human_RBP_ID_24299537 64157 RMVar_ID_64157 Human_SNP_ID_396734244 m1A Human chr9 + 33348077 33348077 33348077 GAGGGATAAAAAACTACACACTGGGTCCGAGCACGGTGGCTCATGCCTATAATCCCAGCACTTTG GAGGGATAAAAAACTACACACTGGGTCCGAGCGCGGTGGCTCATGCCTATAATCCCAGCACTTTG A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33348027..33348166 26863196 MeRIP-seq:(Medium) rs1208272225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18140452 RMVar_hsa_circ_124237,RMVar_hsa_circ_256345,RMVar_hsa_circ_31540,RMVar_hsa_circ_87501,RMVar_hsa_circ_55967,RMVar_hsa_circ_369989,RMVar_hsa_circ_256351,RMVar_hsa_circ_256355,RMVar_hsa_circ_81965,RMVar_hsa_circ_91969,RMVar_hsa_circ_35830,RMVar_hsa_circ_256357,RMVar_hsa_circ_256356,RMVar_hsa_circ_297387,RMVar_hsa_circ_287330,RMVar_hsa_circ_256365,RMVar_hsa_circ_256366,RMVar_hsa_circ_288402,RMVar_hsa_circ_285481,RMVar_hsa_circ_290519,RMVar_hsa_circ_59542 64158 RMVar_ID_64158 Human_SNP_ID_396760871 m1A Human chr9 + 33442475 33442475 33442475 GGCCTCGGGGGACGGGGTTGTTGTAGGGGTCAACAATGGCCAGCACACACACGATAAGGGAGGCT GGCCTCGGGGGACGGGGTTGTTGTAGGGGTCAGCAATGGCCAGCACACACACGATAAGGGAGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33442305..33442522 26863196 MeRIP-seq:(Medium) rs201119765 Functional Loss SNV dbSNP153 33..33 33 - - - 64159 RMVar_ID_64159 Human_SNP_ID_396761028 m1A Human chr9 + 33442907 33442907 33442907 TATCCAAGTGTCCAGAGGGGTAGGTAGCAAAGATGCCGGCTGTGCCATTGGGGCCCGAAACAAAA TATCCAAGTGTCCAGAGGGGTAGGTAGCAAAGGTGCCGGCTGTGCCATTGGGGCCCGAAACAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33442835..33443050 26863196 MeRIP-seq:(Medium) rs758126339 Functional Loss SNV dbSNP153 33..33 33 - - - 64160 RMVar_ID_64160 Human_SNP_ID_396762219 m1A Human chr9 - 33447551 33447551 33447551 CCACCGCCTCCCGCCACCCCTGCCCGCCCGACAGCGCCGCCGCCTGCCCCGCCATGGGTCGACAG CCACCGCCTCCCGCCACCCCTGCCCGCCCGACGGCGCCGCCGCCTGCCCCGCCATGGGTCGACAG T C AQP3 Ensembl:ENSG00000165272 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:33447501..33447600 26863196 MeRIP-seq:(Medium) rs1274678035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037358,Human_RBP_ID_9338885 64161 RMVar_ID_64161 Human_SNP_ID_396762235 m1A Human chr9 + 33447563 33447563 33447563 GGCGGGGCAGGCGGCGGCGCTGTCGGGCGGGCAGGGGTGGCGGGAGGCGGTGGCGCAGCGAGCAG GGCGGGGCAGGCGGCGGCGCTGTCGGGCGGGCCGGGGTGGCGGGAGGCGGTGGCGCAGCGAGCAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:33447462..33447581 26863410 MeRIP-seq:(Medium) rs750110667 Functional Loss SNV dbSNP153 33..33 33 - - - 64162 RMVar_ID_64162 Human_SNP_ID_396762236 m1A Human chr9 + 33447563 33447563 33447563 GGCGGGGCAGGCGGCGGCGCTGTCGGGCGGGCAGGGGTGGCGGGAGGCGGTGGCGCAGCGAGCAG GGCGGGGCAGGCGGCGGCGCTGTCGGGCGGGCGGGGGTGGCGGGAGGCGGTGGCGCAGCGAGCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:33447462..33447581 26863410 MeRIP-seq:(Medium) rs750110667 Functional Loss SNV dbSNP153 33..33 33 - - - 64163 RMVar_ID_64163 Human_SNP_ID_396765952 m1A Human chr9 - 33462048 33462048 33462048 GTGGAGACAGTGGAAAAGAACCGAGGACAGGAAAGGATTGGGTAGGTGAAGGGGTCAGGGGACTG GTGGAGACAGTGGAAAAGAACCGAGGACAGGAGAGGATTGGGTAGGTGAAGGGGTCAGGGGACTG T C NOL6 Ensembl:ENSG00000165271 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33461997..33462110 26863196 MeRIP-seq:(Medium) rs1412954011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797810,Human_RBP_ID_18135091,Human_RBP_ID_18173140,Human_RBP_ID_26565015,Human_RBP_ID_27545553 Human_miRNA_ID_1058911 RMVar_hsa_circ_104163,RMVar_hsa_circ_256375 64164 RMVar_ID_64164 Human_SNP_ID_396769433 m1A Human chr9 - 33472401 33472401 33472401 CTTCTCCCTCACTGGCCACAGGTGATGGAACCAGCCCTGGAAGGCACAGGCAAAGAGGGGAAGAA CTTCTCCCTCACTGGCCACAGGTGATGGAACCGGCCCTGGAAGGCACAGGCAAAGAGGGGAAGAA T C NOL6 Ensembl:ENSG00000165271 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33472351..33472454 26863196 MeRIP-seq:(Medium) rs776159445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975357,Human_RBP_ID_19023758 Human_Splice_Rec_1038494,Human_Splice_Rec_1038544,Human_Splice_Rec_1038584,Human_Splice_Rec_1038630,Human_Splice_Rec_1038642 RMVar_hsa_circ_78268,RMVar_hsa_circ_256387,RMVar_hsa_circ_89417,RMVar_hsa_circ_256388 64165 RMVar_ID_64165 Human_SNP_ID_396778652 m1A Human chr9 - 33511047 33511047 33511047 CGCTGGTGGTGGCCCTTTCCTCAGTCCTGCTGATGTCCTCCAGCTGATTCCAGGCTGTTCCCGGC CGCTGGTGGTGGCCCTTTCCTCAGTCCTGCTGCTGTCCTCCAGCTGATTCCAGGCTGTTCCCGGC T G lnc-BAG1-2,lnc-BAG1-2:2,lnc-BAG1-2:3,lnc-BAG1-2:4,lnc-BAG1-2:5,lnc-BAG1-2:6,lnc-BAG1-2:7,lnc-BAG1-2:8,lnc-BAG1-2:9,lnc-BAG1-2:10 RNACentral:URS0000D57669,RNACentral:URS00008C1EF1,RNACentral:URS00008C3D97,RNACentral:URS00008C194B,RNACentral:URS0000D57B7D,RNACentral:URS0000D5AD64,RNACentral:URS00008C3F07,RNACentral:URS00008C0C09,RNACentral:URS00008C17B7,RNACentral:URS00008C2152 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33510997..33511218 26863196 MeRIP-seq:(Medium) rs1022276950 Functional Loss SNV dbSNP153 33..33 33 - - - 64166 RMVar_ID_64166 Human_SNP_ID_396781808 m1A Human chr9 + 33523995 33523995 33523995 GCCCGGCGGCGGCTGCACCGGGGCAGGAACCGACCCTCAGCCCCATCCCCGCGGACGGTCCCTGG GCCCGGCGGCGGCTGCACCGGGGCAGGAACCGGCCCTCAGCCCCATCCCCGCGGACGGTCCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:33523759..33524280;chr9:33523766..33524121 26863196 MeRIP-seq:(Medium) rs1311490683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27545582 64167 RMVar_ID_64167 Human_SNP_ID_396782006 m1A Human chr9 - 33524541 33524541 33524541 GTACCCCCGACCCGCATACTCTTGGTCCATGGAGCTCAGGAGCGCCTGGCCCAGGCGTCTCCCAA GTACCCCCGACCCGCATACTCTTGGTCCATGGTGCTCAGGAGCGCCTGGCCCAGGCGTCTCCCAA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:33524435..33524625 26863196 MeRIP-seq:(Medium) rs1245119200 Functional Loss SNV dbSNP153 33..33 33 - - - 64168 RMVar_ID_64168 Human_SNP_ID_396795203 m1A Human chr9 + 33581790 33581790 33581790 GGGCGGGGAGGGTGGGGAGGAATAGGCTGGCCATAGGGTGGTGGGTAGTAGGAAGGGGGAGTAGC GGGCGGGGAGGGTGGGGAGGAATAGGCTGGCCGTAGGGTGGTGGGTAGTAGGAAGGGGGAGTAGC A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33581781..33581911 26863196 MeRIP-seq:(Medium) rs1464372837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3911526,Human_RBP_ID_7922178,Human_RBP_ID_9442245 64169 RMVar_ID_64169 Human_SNP_ID_396795204 m1A Human chr9 + 33581792 33581792 33581792 GCGGGGAGGGTGGGGAGGAATAGGCTGGCCATAGGGTGGTGGGTAGTAGGAAGGGGGAGTAGCCT GCGGGGAGGGTGGGGAGGAATAGGCTGGCCATGGGGTGGTGGGTAGTAGGAAGGGGGAGTAGCCT A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33581789..33581935 26863196 MeRIP-seq:(Medium) rs1335630460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3911526,Human_RBP_ID_7922178,Human_RBP_ID_9442245 64170 RMVar_ID_64170 Human_SNP_ID_396795237 m1A Human chr9 + 33581884 33581884 33581884 CCTCTACTAGGACAGTGCACCTGTGGCTTTGCAGGCTTTAGCCCCGTGGCTGCTCTCATGGGCTT CCTCTACTAGGACAGTGCACCTGTGGCTTTGCCGGCTTTAGCCCCGTGGCTGCTCTCATGGGCTT A C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33581826..33581919 26863196 MeRIP-seq:(Medium) rs556280223 Functional Loss SNV dbSNP153 33..33 33 - - - 64171 RMVar_ID_64171 Human_SNP_ID_396795964 m1A Human chr9 - 33584862 33584862 33584862 TCACACCACCCTACAGCCAACCTACTCCTCTGACCTTACCCACTTCTGTTTACTTCCAACTCCAC TCACACCACCCTACAGCCAACCTACTCCTCTGGCCTTACCCACTTCTGTTTACTTCCAACTCCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33584778..33584912 26863196 MeRIP-seq:(Medium) rs1462777964 Functional Loss SNV dbSNP153 33..33 33 - - - 64172 RMVar_ID_64172 Human_SNP_ID_396795966 m1A Human chr9 + 33584864 33584864 33584864 GGAGTTGGAAGTAAACAGAAGTGGGTAAGGTCAGAGGAGTAGGTTGGCTGTAGGGTGGTGTGAGG GGAGTTGGAAGTAAACAGAAGTGGGTAAGGTCGGAGGAGTAGGTTGGCTGTAGGGTGGTGTGAGG A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33584766..33584877 26863196 MeRIP-seq:(Medium) rs1748865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7922180 64173 RMVar_ID_64173 Human_SNP_ID_396797597 m1A Human chr9 - 33590958 33590958 33590958 TCAATCAGCTCCCACCAGGCCCCACCTCCAACATTCAGGAATACAATTTCCCATGATCTTTTGTA TCAATCAGCTCCCACCAGGCCCCACCTCCAACGTTCAGGAATACAATTTCCCATGATCTTTTGTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33590907..33591130 26863196 MeRIP-seq:(Medium) rs562153 Functional Loss SNV dbSNP153 33..33 33 - - - 64174 RMVar_ID_64174 Human_SNP_ID_396799142 m1A Human chr9 - 33597114 33597104 33597114 CTCCTCCTGCCATGATTAAATCACCTCCCACCAGGCCCCACCTCCAACATTAAGGAGTACATTCC CTCCTCCTGCCATGATTAAATCACCTCCCACC__________TCCAACATTAAGGAGTACATTCC AGGTGGGGCCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33597065..33597140 26863196 MeRIP-seq:(Medium) rs1411699131 Functional Loss DEL dbSNP153 33..42 33 - - - 64175 RMVar_ID_64175 Human_SNP_ID_396799526 m1A Human chr9 - 33598546 33598546 33598546 CGCTGACCAGGTCCCTGCTGACCATATCCCGCACATCAGGTCCTTCCTGACCACACCCTCACTGA CGCTGACCAGGTCCCTGCTGACCATATCCCGCCCATCAGGTCCTTCCTGACCACACCCTCACTGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33598498..33598600 26863196 MeRIP-seq:(Medium) rs1392714129 Functional Loss SNV dbSNP153 33..33 33 - - - 64176 RMVar_ID_64176 Human_SNP_ID_396813927 m1A Human chr9 - 33658660 33658660 33658660 GACAGCTGAACCCTCATGGAGCCATTCATACAAGTCCCTATTTAAGGAACAAGTGATTATGCTAC GACAGCTGAACCCTCATGGAGCCATTCATACAGGTCCCTATTTAAGGAACAAGTGATTATGCTAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33658564..33658785 26863196 MeRIP-seq:(Medium) rs77401176 Functional Loss SNV dbSNP153 33..33 33 - - - 64177 RMVar_ID_64177 Human_SNP_ID_396851250 m1A Human chr9 - 33817227 33817226 33817227 CGCGGCGGTGGCGGCGGGGGCTGCGCGGGGGGAGGGGCGACGGCGGAGGAGGAGGAGAGCGAGAG CGCGGCGGTGGCGGCGGGGGCTGCGCGGGGGG_GGGGCGACGGCGGAGGAGGAGGAGAGCGAGAG CT C UBE2R2-AS1 Ensembl:ENSG00000235481 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:33817176..33817550 26863196 MeRIP-seq:(Medium) rs1447750749 Functional Loss DEL dbSNP153 33..33 33 - - - 64178 RMVar_ID_64178 Human_SNP_ID_396851251 m1A Human chr9 - 33817227 33817227 33817227 CGCGGCGGTGGCGGCGGGGGCTGCGCGGGGGGAGGGGCGACGGCGGAGGAGGAGGAGAGCGAGAG CGCGGCGGTGGCGGCGGGGGCTGCGCGGGGGGGGGGGCGACGGCGGAGGAGGAGGAGAGCGAGAG T C UBE2R2-AS1 Ensembl:ENSG00000235481 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:33817176..33817550 26863196 MeRIP-seq:(Medium) rs977797728 Functional Loss SNV dbSNP153 33..33 33 - - - 64179 RMVar_ID_64179 Human_SNP_ID_396851299 m1A Human chr9 + 33817330 33817330 33817330 CCCGCGCGCCCTCCGGCCCCTGCGGCCCCCGAAGAGAACGAGAGGGCGAGCGAGCGCGGCGTTCC CCCGCGCGCCCTCCGGCCCCTGCGGCCCCCGACGAGAACGAGAGGGCGAGCGAGCGCGGCGTTCC A C UBE2R2 Ensembl:ENSG00000107341 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:33817151..33886925 26863196 MeRIP-seq:(Medium) rs1343495104 Functional Loss SNV dbSNP153 33..33 33 - - - 64180 RMVar_ID_64180 Human_SNP_ID_396851369 m1A Human chr9 - 33817457 33817457 33817457 ACGGGTCCCGGTCCCGGGCCTCCCCCCCCCGGAGGGGGCCTCAACTTGGGGGGGGGGAGAGGAGG ACGGGTCCCGGTCCCGGGCCTCCCCCCCCCGGGGGGGGCCTCAACTTGGGGGGGGGGAGAGGAGG T C UBE2R2-AS1 Ensembl:ENSG00000235481 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:33817224..33817467 32194978 MeRIP-seq:(Medium) rs1243179292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8275633 64181 RMVar_ID_64181 Human_SNP_ID_396873350 m1A Human chr9 + 33900230 33900230 33900230 CTTCATCCGCCTGTAGATGACCCACAGAGTGGAGAACTGCCTTCTGAAAGGTGGAATCCTACTCA CTTCATCCGCCTGTAGATGACCCACAGAGTGGGGAACTGCCTTCTGAAAGGTGGAATCCTACTCA A G UBE2R2 Ensembl:ENSG00000107341 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:33900201..33900275 26863196 MeRIP-seq:(Medium) rs924179172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717853,Human_RBP_ID_1704878,Human_RBP_ID_2063988,Human_RBP_ID_16659451,Human_RBP_ID_17322836,Human_RBP_ID_21906874,Human_RBP_ID_22518247,Human_RBP_ID_24299913 Human_Splice_Rec_1038880,Human_Splice_Rec_1038881 Human_miRNA_ID_2279661,Human_miRNA_ID_2459722,Human_miRNA_ID_2639951,Human_miRNA_ID_2931846 RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_271389,RMVar_hsa_circ_256399,RMVar_hsa_circ_256401,RMVar_hsa_circ_269972 64182 RMVar_ID_64182 Human_SNP_ID_396878020 m1A Human chr9 + 33919309 33919309 33919309 GTGCTGATTTACCTCCCCCAAAATGCCCCCAAACCCCCATGCAAGTTTACAGCCAGTAGCTTGGT GTGCTGATTTACCTCCCCCAAAATGCCCCCAATCCCCCATGCAAGTTTACAGCCAGTAGCTTGGT A T UBE2R2 Ensembl:ENSG00000107341 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33919260..33919348 26863196 MeRIP-seq:(Medium) rs1030947938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18135203 64183 RMVar_ID_64183 Human_SNP_ID_396878110 m1A Human chr9 + 33919606 33919606 33919606 TGATGAGTACAATCAGTTCCAGAAGACTGGGTAAGTCTCTTGCTAGCAGGTGGACATTCTGGTAT TGATGAGTACAATCAGTTCCAGAAGACTGGGTGAGTCTCTTGCTAGCAGGTGGACATTCTGGTAT A G UBE2R2 Ensembl:ENSG00000107341 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:33919509..33919609 32194978 MeRIP-seq:(Medium) rs1357657498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2064001,Human_RBP_ID_7922579,Human_RBP_ID_8703655 64184 RMVar_ID_64184 Human_SNP_ID_396881758 m1A Human chr9 + 33931807 33931807 33931807 GTTTCCTGCCTCCTCCATTCGTCTGCACCCTAATCCTTCCTCCCAGCCTGTGGACCTGCCTACTC GTTTCCTGCCTCCTCCATTCGTCTGCACCCTAGTCCTTCCTCCCAGCCTGTGGACCTGCCTACTC A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33931805..33932182 26863196 MeRIP-seq:(Medium) rs1228600076 Functional Loss SNV dbSNP153 33..33 33 - - - 64185 RMVar_ID_64185 Human_SNP_ID_396882215 m1A Human chr9 + 33933550 33933550 33933550 TCAGGTCGCCAGTGTGCTGGGATGTGGACGGCAGAAGTGCAGTGCAGGAGGTGGTGCTGGGCAGG TCAGGTCGCCAGTGTGCTGGGATGTGGACGGCCGAAGTGCAGTGCAGGAGGTGGTGCTGGGCAGG A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:33933450..33933613 26863196 MeRIP-seq:(Medium) rs1416426783 Functional Loss SNV dbSNP153 33..33 33 - - - 64186 RMVar_ID_64186 Human_SNP_ID_396884813 m1A Human chr9 - 33941761 33941761 33941761 TACCTCCTGCAGTCTGACAAGCTCATCACTGAATTCTGCTAGTCCAGTAGCAATGTCTTCCTCTT TACCTCCTGCAGTCTGACAAGCTCATCACTGAGTTCTGCTAGTCCAGTAGCAATGTCTTCCTCTT T C UBAP2 Ensembl:ENSG00000137073 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs307658 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_961331,Human_RBP_ID_9406861,Human_RBP_ID_17322839,Human_RBP_ID_18908164,Human_RBP_ID_21720118,Human_RBP_ID_27832326 Human_miRNA_ID_2541771,Human_miRNA_ID_2543647,Human_miRNA_ID_2547352,Human_miRNA_ID_2549216,Human_miRNA_ID_2551085,Human_miRNA_ID_2556490,Human_miRNA_ID_2558372,Human_miRNA_ID_2588791 GWAS_ID_7853,GWAS_ID_7854,GWAS_ID_7855,GWAS_ID_7856,GWAS_ID_7857,GWAS_ID_7858,GWAS_ID_7859,GWAS_ID_7860,GWAS_ID_7861,GWAS_ID_7862,GWAS_ID_7863 RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_256405,RMVar_hsa_circ_97502,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_89057,RMVar_hsa_circ_15047,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_111717,RMVar_hsa_circ_256413,RMVar_hsa_circ_256414,RMVar_hsa_circ_377085,RMVar_hsa_circ_256415,RMVar_hsa_circ_377386,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_119979,RMVar_hsa_circ_256418,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_256422,RMVar_hsa_circ_116561,RMVar_hsa_circ_351025,RMVar_hsa_circ_352118,RMVar_hsa_circ_369653,RMVar_hsa_circ_278531,RMVar_hsa_circ_87127,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256433,RMVar_hsa_circ_301404,RMVar_hsa_circ_256425,RMVar_hsa_circ_256427,RMVar_hsa_circ_256428,RMVar_hsa_circ_256429,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_322683,RMVar_hsa_circ_374778,RMVar_hsa_circ_316868,RMVar_hsa_circ_53464,RMVar_hsa_circ_288073,RMVar_hsa_circ_289056,RMVar_hsa_circ_272780,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_256434,RMVar_hsa_circ_256431,RMVar_hsa_circ_256432,RMVar_hsa_circ_256430 64187 RMVar_ID_64187 Human_SNP_ID_396897847 m1A Human chr9 - 33989022 33989022 33989022 GAGAAGAAAAGCGAGAAAGAATCGAGTCGTGGACGTGGAAACAACAACCGGAAAGGAAGAGGCGG GAGAAGAAAAGCGAGAAAGAATCGAGTCGTGGTCGTGGAAACAACAACCGGAAAGGAAGAGGCGG T A UBAP2 Ensembl:ENSG00000137073 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:33988935..33989060;chr9:33988925..33989100;chr9:33988913..33989150;chr9:33988921..33989064 26863196 MeRIP-seq:(Medium) rs746418891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91291,Human_RBP_ID_3975369,Human_RBP_ID_5634095,Human_RBP_ID_9406863,Human_RBP_ID_16661329,Human_RBP_ID_24300119,Human_RBP_ID_26360644,Human_RBP_ID_27545654,Human_RBP_ID_27832338 Human_Splice_Rec_1038917,Human_Splice_Rec_1038973,Human_Splice_Rec_1039045,Human_Splice_Rec_1039127,Human_Splice_Rec_1039141 RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_119979,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_374778,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_71252,RMVar_hsa_circ_10739,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_288215,RMVar_hsa_circ_256468,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256477,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,RMVar_hsa_circ_297790,RMVar_hsa_circ_275675,RMVar_hsa_circ_80358,RMVar_hsa_circ_256479,RMVar_hsa_circ_256480,RMVar_hsa_circ_256478,RMVar_hsa_circ_323107,RMVar_hsa_circ_256484,RMVar_hsa_circ_270594,RMVar_hsa_circ_288116,RMVar_hsa_circ_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256486,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 64188 RMVar_ID_64188 Human_SNP_ID_396899923 m1A Human chr9 + 33996173 33996173 33996173 ACCCCCAAACAAGGTGAAGTTGAAAATGTGCTACGGAATTGGAGACAAATGTAAACAATGCAAAT ACCCCCAAACAAGGTGAAGTTGAAAATGTGCTGCGGAATTGGAGACAAATGTAAACAATGCAAAT A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33996169..33996274 26863196 MeRIP-seq:(Medium) rs1312318582 Functional Loss SNV dbSNP153 33..33 33 - - - 64189 RMVar_ID_64189 Human_SNP_ID_396914023 m1A Human chr9 + 34043031 34043031 34043031 TAGAGGCTGCAGTGAGCCATGATCATGCCAAGACACTCCATCCTGGGCGACAAAGCAAGACCCTG TAGAGGCTGCAGTGAGCCATGATCATGCCAAGGCACTCCATCCTGGGCGACAAAGCAAGACCCTG A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:34043027..34043179 26863196 MeRIP-seq:(Medium) rs1005435187 Functional Loss SNV dbSNP153 33..33 33 - - - 64190 RMVar_ID_64190 Human_SNP_ID_396914034 m1A Human chr9 - 34043064 34043064 34043064 TAAACACATATGTAGAGTTGTTTTTTTTGGAGACAGGGTCTTGCTTTGTCGCCCAGGATGGAGTG TAAACACATATGTAGAGTTGTTTTTTTTGGAGGCAGGGTCTTGCTTTGTCGCCCAGGATGGAGTG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34043059..34043232 26863196 MeRIP-seq:(Medium) rs1413906072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16662932 RMVar_hsa_circ_87464,RMVar_hsa_circ_256449,RMVar_hsa_circ_256481,RMVar_hsa_circ_80358,RMVar_hsa_circ_121180,RMVar_hsa_circ_256490 64191 RMVar_ID_64191 Human_SNP_ID_396915766 m1A Human chr9 - 34048772 34048772 34048772 CTCCTTCCCTCTTCCAGGGCCCTGAGCGCTGCAGCGTGTGCTTTCTAATTCTGGGTTCAGCTCGT CTCCTTCCCTCTTCCAGGGCCCTGAGCGCTGCCGCGTGTGCTTTCTAATTCTGGGTTCAGCTCGT T G UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:34048768..34048839 26863196 MeRIP-seq:(Medium) rs1322448827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87464,RMVar_hsa_circ_256449,RMVar_hsa_circ_256481,RMVar_hsa_circ_80358,RMVar_hsa_circ_121180,RMVar_hsa_circ_256490 64192 RMVar_ID_64192 Human_SNP_ID_396926070 m1A Human chr9 + 34087481 34087481 34087481 GAGAAGCTAGGATGGGGATTCAAGTCCCATGAAGCCTTTTGTAGCCTCTGGAGCTGCACCTGGAT GAGAAGCTAGGATGGGGATTCAAGTCCCATGACGCCTTTTGTAGCCTCTGGAGCTGCACCTGGAT A C AL354989.1 Ensembl:ENSG00000228352 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:34087433..34087833 32194978 MeRIP-seq:(Medium) rs1182629946 Functional Loss SNV dbSNP153 33..33 33 - - - 64193 RMVar_ID_64193 Human_SNP_ID_396950396 m1A Human chr9 - 34179674 34179674 34179674 ACCTCTGGTCTAGTCTCCACCTTTTCTCCCCAATCTCATTGCCTCAGGGAGAACTAAATCTACAC ACCTCTGGTCTAGTCTCCACCTTTTCTCCCCAGTCTCATTGCCTCAGGGAGAACTAAATCTACAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:34179428..34179690 26863196 MeRIP-seq:(Medium) rs567697156 Functional Loss SNV dbSNP153 33..33 33 - - - 64194 RMVar_ID_64194 Human_SNP_ID_397000546 m1A Human chr9 - 34372453 34372452 34372453 GGACACGGTCATGTGCTACCGCGTGCGCTGGGAGGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG GGACACGGTCATGTGCTACCGCGTGCGCTGGG_GGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG CT C MYORG Ensembl:ENSG00000164976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34372402..34372485 26863196 MeRIP-seq:(Medium) rs1563982623 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5035656,Human_RBP_ID_22466340,Human_RBP_ID_22776822 RMVar_hsa_circ_122503,RMVar_hsa_circ_256520,RMVar_hsa_circ_77430,RMVar_hsa_circ_256519 64195 RMVar_ID_64195 Human_SNP_ID_397000547 m1A Human chr9 - 34372453 34372453 34372453 GGACACGGTCATGTGCTACCGCGTGCGCTGGGAGGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG GGACACGGTCATGTGCTACCGCGTGCGCTGGGGGGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG T C MYORG Ensembl:ENSG00000164976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34372402..34372485 26863196 MeRIP-seq:(Medium) rs745363481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035656,Human_RBP_ID_22466340,Human_RBP_ID_22776822 RMVar_hsa_circ_122503,RMVar_hsa_circ_256520,RMVar_hsa_circ_77430,RMVar_hsa_circ_256519 64196 RMVar_ID_64196 Human_SNP_ID_397000548 m1A Human chr9 - 34372453 34372453 34372453 GGACACGGTCATGTGCTACCGCGTGCGCTGGGAGGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG GGACACGGTCATGTGCTACCGCGTGCGCTGGGCGGAGGCAGCGCCGGGCCGGGCCGTGGAGCACG T G MYORG Ensembl:ENSG00000164976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34372402..34372485 26863196 MeRIP-seq:(Medium) rs745363481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035656,Human_RBP_ID_22466340,Human_RBP_ID_22776822 RMVar_hsa_circ_122503,RMVar_hsa_circ_256520,RMVar_hsa_circ_77430,RMVar_hsa_circ_256519 64197 RMVar_ID_64197 Human_SNP_ID_397000878 m1A Human chr9 - 34372921 34372921 34372921 CAGCCCACTAATGCTCCAGAACCCTCAGGAGAAGAGCCAGGCCTACCCCCGCCGCCGCCGGCCTG CAGCCCACTAATGCTCCAGAACCCTCAGGAGACGAGCCAGGCCTACCCCCGCCGCCGCCGGCCTG T G MYORG Ensembl:ENSG00000164976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34372871..34372971 26863196 MeRIP-seq:(Medium) rs748981258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797764,Human_RBP_ID_5035658 Human_Splice_Rec_1039326 RMVar_hsa_circ_77430,RMVar_hsa_circ_256519 64198 RMVar_ID_64198 Human_SNP_ID_397007193 m1A Human chr9 + 34399355 34399351 34399355 AGGGGTGGGCCTTCCTCACCTCTTCCCTCTTGATTTTCAGTCTCAGCTTTCCAGTCCCCTCCCCC AGGGGTGGGCCTTCCTCACCTCTTCCCTC____TTTTCAGTCTCAGCTTTCCAGTCCCCTCCCCC CTTGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34399304..34399426 26863196 MeRIP-seq:(Medium) rs1398679276 Functional Loss DEL dbSNP153 30..33 33 - - - 64199 RMVar_ID_64199 Human_SNP_ID_397009348 m1A Human chr9 - 34408663 34408663 34408663 GCTCCCCAAGGAGAGAGAGGAGGGCCAAGGGCAGGACCCTACAGAGGAGGCAAAGGGTTGTGGGA GCTCCCCAAGGAGAGAGAGGAGGGCCAAGGGCGGGACCCTACAGAGGAGGCAAAGGGTTGTGGGA T C FAM219A Ensembl:ENSG00000164970 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34408660..34408725 26863196 MeRIP-seq:(Medium) rs1474217491 Functional Loss SNV dbSNP153 33..33 33 - - - 64200 RMVar_ID_64200 Human_SNP_ID_397019360 m1A Human chr9 - 34453470 34453470 34453470 TTTTAGATATATGTCAAAAAGAGTAGAGATCAATGAAGTGTCATGAGAAAGAGTGACACCCTGCT TTTTAGATATATGTCAAAAAGAGTAGAGATCAGTGAAGTGTCATGAGAAAGAGTGACACCCTGCT T C FAM219A Ensembl:ENSG00000164970 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34453464..34453529 26863196 MeRIP-seq:(Medium) rs1482430291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3212165,Human_RBP_ID_16665765 64201 RMVar_ID_64201 Human_SNP_ID_397057828 m1A Human chr9 - 34611317 34611317 34611317 CTGATGCTTCCCTGCAGTGGGCAGCGAGAGTCACAGACAAGACAGCAAGCAGGATGGAGCACTAC CTGATGCTTCCCTGCAGTGGGCAGCGAGAGTCGCAGACAAGACAGCAAGCAGGATGGAGCACTAC T C RPP25L Ensembl:ENSG00000164967 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:34611051..34611350;chr9:34610994..34612075;chr9:34611043..34612069;chr9:34611228..34612068 26863196 MeRIP-seq:(Medium) rs766953049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036135,Human_RBP_ID_16666087,Human_RBP_ID_27545766 Human_Splice_Rec_1039722,Human_Splice_Rec_1039724 64202 RMVar_ID_64202 Human_SNP_ID_397058533 m1A Human chr9 - 34614083 34614083 34614083 CTTTGGCCCTACAGGACCAGTGTGTGGAAATCACTGAGGAGTCCAAGGCTCTCCTGGAGGAATAC CTTTGGCCCTACAGGACCAGTGTGTGGAAATCCCTGAGGAGTCCAAGGCTCTCCTGGAGGAATAC T G DCTN3 Ensembl:ENSG00000137100 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:34614043..34614143 32194978 MeRIP-seq:(Medium) rs370374770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718157,Human_RBP_ID_2064158,Human_RBP_ID_5027023 Human_Splice_Rec_1039732,Human_Splice_Rec_1039733,Human_Splice_Rec_1039736,Human_Splice_Rec_1039737,Human_Splice_Rec_1039748,Human_Splice_Rec_1039749,Human_Splice_Rec_1039751,Human_Splice_Rec_1039760,Human_Splice_Rec_1039761,Human_Splice_Rec_1039773,Human_Splice_Rec_1039786,Human_Splice_Rec_1039790 Human_miRNA_ID_1272010 RMVar_hsa_circ_80503,RMVar_hsa_circ_103776,RMVar_hsa_circ_120556,RMVar_hsa_circ_123533,RMVar_hsa_circ_110603,RMVar_hsa_circ_93615,RMVar_hsa_circ_256525,RMVar_hsa_circ_256527,RMVar_hsa_circ_256528,RMVar_hsa_circ_256529,RMVar_hsa_circ_256526,RMVar_hsa_circ_256524 64203 RMVar_ID_64203 Human_SNP_ID_397058743 m1A Human chr9 - 34614770 34614770 34614770 AGCATCATCCAGCAGTGTGTGTTGTGTTTTACAGCCGTTCCTGAGCATGCTGCCCGCCTGCAGCG AGCATCATCCAGCAGTGTGTGTTGTGTTTTACGGCCGTTCCTGAGCATGCTGCCCGCCTGCAGCG T C DCTN3 Ensembl:ENSG00000137100 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:34614740..34614841 32194978 MeRIP-seq:(Medium) rs1564086787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22691062 Human_Splice_Rec_1039731,Human_Splice_Rec_1039735,Human_Splice_Rec_1039747,Human_Splice_Rec_1039759,Human_Splice_Rec_1039771,Human_Splice_Rec_1039783,Human_Splice_Rec_1039785,Human_Splice_Rec_1039789 RMVar_hsa_circ_80503,RMVar_hsa_circ_123533,RMVar_hsa_circ_110603,RMVar_hsa_circ_256527,RMVar_hsa_circ_256528,RMVar_hsa_circ_256529 64204 RMVar_ID_64204 Human_SNP_ID_397059054 m1A Human chr9 + 34616080 34616080 34616080 CCAGCATGGGCACCAAGGCATTCACCTGCTCCAGGAGTGCAACCTGGGAAAGGATAAACTGCTCC CCAGCATGGGCACCAAGGCATTCACCTGCTCCTGGAGTGCAACCTGGGAAAGGATAAACTGCTCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:34616026..34616100 32194978 MeRIP-seq:(Medium) rs1463881300 Functional Loss SNV dbSNP153 33..33 33 - - - 64205 RMVar_ID_64205 Human_SNP_ID_397059650 m1A Human chr9 - 34618706 34618706 34618706 TGCAGGTGGCTTTGGGGAACATTTCCAGCAAGAGGGAGAGGGTGAAGATTCTCTACAAAAAGAGT TGCAGGTGGCTTTGGGGAACATTTCCAGCAAGCGGGAGAGGGTGAAGATTCTCTACAAAAAGAGT T G DCTN3 Ensembl:ENSG00000137100 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:34618676..34618775 32194978 MeRIP-seq:(Medium) rs1370744586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718161,Human_RBP_ID_961337,Human_RBP_ID_8944615 Human_Splice_Rec_1039726,Human_Splice_Rec_1039727,Human_Splice_Rec_1039740,Human_Splice_Rec_1039741,Human_Splice_Rec_1039754,Human_Splice_Rec_1039755,Human_Splice_Rec_1039764,Human_Splice_Rec_1039765,Human_Splice_Rec_1039776,Human_Splice_Rec_1039777,Human_Splice_Rec_1039792,Human_Splice_Rec_1039793,Human_Splice_Rec_1039800,Human_Splice_Rec_1039801 RMVar_hsa_circ_80503,RMVar_hsa_circ_110603,RMVar_hsa_circ_256528,RMVar_hsa_circ_256529 64206 RMVar_ID_64206 Human_SNP_ID_397060032 m1A Human chr9 + 34620403 34620403 34620403 TCCGTGAGCCGCGCGCCCCGCCCGGCCCGTACACCCAGCGCTCCAGCTCTTCCACTCGGGCCTGT TCCGTGAGCCGCGCGCCCCGCCCGGCCCGTACGCCCAGCGCTCCAGCTCTTCCACTCGGGCCTGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:34620298..34620500 26863196 MeRIP-seq:(Medium) rs780419837 Functional Loss SNV dbSNP153 33..33 33 - - - 64207 RMVar_ID_64207 Human_SNP_ID_397060060 m1A Human chr9 - 34620442 34620442 34620442 GGTAGTAGCGATGGCGGGTCTGACTGACTTGCAGCGGCTACAGGCCCGAGTGGAAGAGCTGGAGC GGTAGTAGCGATGGCGGGTCTGACTGACTTGCGGCGGCTACAGGCCCGAGTGGAAGAGCTGGAGC T C DCTN3 Ensembl:ENSG00000137100 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:34617961..34620500;chr9:34620326..34620500;chr9:34617926..34620500 26863196 MeRIP-seq:(Medium) rs961742356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036138,Human_RBP_ID_24300931 Human_Splice_Rec_1039725,Human_Splice_Rec_1039739,Human_Splice_Rec_1039753,Human_Splice_Rec_1039763,Human_Splice_Rec_1039775,Human_Splice_Rec_1039791,Human_Splice_Rec_1039799 RMVar_hsa_circ_110603,RMVar_hsa_circ_256529 64208 RMVar_ID_64208 Human_SNP_ID_397060061 m1A Human chr9 - 34620442 34620442 34620442 GGTAGTAGCGATGGCGGGTCTGACTGACTTGCAGCGGCTACAGGCCCGAGTGGAAGAGCTGGAGC GGTAGTAGCGATGGCGGGTCTGACTGACTTGCCGCGGCTACAGGCCCGAGTGGAAGAGCTGGAGC T G DCTN3 Ensembl:ENSG00000137100 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:34617961..34620500;chr9:34620326..34620500;chr9:34617926..34620500 26863196 MeRIP-seq:(Medium) rs961742356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036138,Human_RBP_ID_24300931 Human_Splice_Rec_1039725,Human_Splice_Rec_1039739,Human_Splice_Rec_1039753,Human_Splice_Rec_1039763,Human_Splice_Rec_1039775,Human_Splice_Rec_1039791,Human_Splice_Rec_1039799 RMVar_hsa_circ_110603,RMVar_hsa_circ_256529 64209 RMVar_ID_64209 Human_SNP_ID_397062189 m1A Human chr9 - 34627833 34627831 34627834 TGAGGAAGAGGAAGATGCTGAAGAAGATGAGGAGAAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG TGAGGAAGAGGAAGATGCTGAAGAAGATGAG___AAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG TCTC T ARID3C Ensembl:ENSG00000205143 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:34627713..34628077;chr9:34627739..34627961 26863196 MeRIP-seq:(Medium) rs1418926018 Functional Loss DEL dbSNP153 32..34 33 - - - 64210 RMVar_ID_64210 Human_SNP_ID_397062190 m1A Human chr9 - 34627833 34627833 34627833 TGAGGAAGAGGAAGATGCTGAAGAAGATGAGGAGAAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG TGAGGAAGAGGAAGATGCTGAAGAAGATGAGGTGAAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG T A ARID3C Ensembl:ENSG00000205143 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:34627713..34628077;chr9:34627739..34627961 26863196 MeRIP-seq:(Medium) rs370515839 Functional Loss SNV dbSNP153 33..33 33 - - - 64211 RMVar_ID_64211 Human_SNP_ID_397062191 m1A Human chr9 - 34627833 34627833 34627833 TGAGGAAGAGGAAGATGCTGAAGAAGATGAGGAGAAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG TGAGGAAGAGGAAGATGCTGAAGAAGATGAGGCGAAGCGGGAGGAAGCCGGGGCAGAGGAGGAGG T G ARID3C Ensembl:ENSG00000205143 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:34627713..34628077;chr9:34627739..34627961 26863196 MeRIP-seq:(Medium) rs370515839 Functional Loss SNV dbSNP153 33..33 33 - - - 64212 RMVar_ID_64212 Human_SNP_ID_397063830 m1A Human chr9 - 34634832 34634817 34634832 CTGGCCTGGAGAAGGCCTTTTACACACACACAACACATACACACACACACACACACACACATATC CTGGCCTGGAGAAGGCCTTTTACACACACACA_______________CACACACACACACATATC GTGTGTGTGTATGTGT G SIGMAR1 Ensembl:ENSG00000147955 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34634783..34634859 26863196 MeRIP-seq:(Medium) rs1193045550 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_218768,Human_RBP_ID_8275232,Human_RBP_ID_9441900,Human_RBP_ID_17322093,Human_RBP_ID_17436317,Human_RBP_ID_17549606,Human_RBP_ID_18521197,Human_RBP_ID_18542007,Human_RBP_ID_27545774 RMVar_hsa_circ_104684,RMVar_hsa_circ_108807,RMVar_hsa_circ_256531,RMVar_hsa_circ_256532 64213 RMVar_ID_64213 Human_SNP_ID_397063884 m1A Human chr9 - 34635051 34635051 34635051 TGCTATGCAAGTGCCCCTGTGGCTTGTCCCCAACCCCCTCAGCAACAAAGCTCAGCTGGGGAACG TGCTATGCAAGTGCCCCTGTGGCTTGTCCCCAGCCCCCTCAGCAACAAAGCTCAGCTGGGGAACG T C SIGMAR1 Ensembl:ENSG00000147955 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:34635001..34635075 26863196 MeRIP-seq:(Medium) rs1466448950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_218769,Human_RBP_ID_718184,Human_RBP_ID_797591,Human_RBP_ID_1403251,Human_RBP_ID_5027070,Human_RBP_ID_8224519,Human_RBP_ID_9441901,Human_RBP_ID_17094589,Human_RBP_ID_17323427,Human_RBP_ID_17437293,Human_RBP_ID_17550677,Human_RBP_ID_17579649,Human_RBP_ID_17666476,Human_RBP_ID_18961968,Human_RBP_ID_24300950,Human_RBP_ID_26563530,Human_RBP_ID_27136125,Human_RBP_ID_27374934 RMVar_hsa_circ_104684,RMVar_hsa_circ_108807,RMVar_hsa_circ_256531,RMVar_hsa_circ_256532 64214 RMVar_ID_64214 Human_SNP_ID_397064017 m1A Human chr9 + 34635602 34635602 34635602 GTGGATATGTGCGGGCCTGCCCGCTCCTGTCTATCCGCAGGTCTTCCTTCAGGCCTGGCTGGTCA GTGGATATGTGCGGGCCTGCCCGCTCCTGTCTCTCCGCAGGTCTTCCTTCAGGCCTGGCTGGTCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:34635551..34636761 32194978 MeRIP-seq:(Medium) rs764760106 Functional Loss SNV dbSNP153 33..33 33 - - - 64215 RMVar_ID_64215 Human_SNP_ID_397064099 m1A Human chr9 - 34635804 34635804 34635804 TGGTGAGGCAACAGCTGTGGAGTGGGGGCCAAACACATGGATGGTGGAGTACGGCCGGGGCGTCA TGGTGAGGCAACAGCTGTGGAGTGGGGGCCAATCACATGGATGGTGGAGTACGGCCGGGGCGTCA T A SIGMAR1 Ensembl:ENSG00000147955 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:34635327..34635881;chr9:34635533..34635874 26863196 MeRIP-seq:(Medium) rs766761162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847454,Human_RBP_ID_1059160,Human_RBP_ID_18135428,Human_RBP_ID_18472876,Human_RBP_ID_22776824,Human_RBP_ID_27136136 Human_Splice_Rec_1039818,Human_Splice_Rec_1039824,Human_Splice_Rec_1039830,Human_Splice_Rec_1039834,Human_Splice_Rec_1039836,Human_Splice_Rec_1039840 GWAS_ID_7864 RMVar_hsa_circ_104684,RMVar_hsa_circ_108807,RMVar_hsa_circ_256531,RMVar_hsa_circ_256532 64216 RMVar_ID_64216 Human_SNP_ID_397064590 m1A Human chr9 + 34637378 34637378 34637378 CGGGCAGCACGTGGCCTGGGTGCAGCCGCCGCAGCTCCACGATCAGACGAGAGAAGGCCAGCTCG CGGGCAGCACGTGGCCTGGGTGCAGCCGCCGCTGCTCCACGATCAGACGAGAGAAGGCCAGCTCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:34637250..34637535 26863196 MeRIP-seq:(Medium) rs140376902 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_246 GWAS_ID_7865 64217 RMVar_ID_64217 Human_SNP_ID_397064738 m1A Human chr9 - 34637712 34637712 34637712 GGCCCCGGCTCCCTCCTGAGCTGCGCCGTGCCAGGCCGCCCGCCGGGATGCAGTGGGCCGTGGGC GGCCCCGGCTCCCTCCTGAGCTGCGCCGTGCCCGGCCGCCCGCCGGGATGCAGTGGGCCGTGGGC T G SIGMAR1 Ensembl:ENSG00000147955 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEK293T,untreat control;HEPG2 cell line,mRNA untreated chr9:34637551..34637800;chr9:34637666..34637757;chr9:34637182..34637825 26863410,26863196 MeRIP-seq:(Medium) rs1246401025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256697,Human_RBP_ID_5027145,Human_RBP_ID_5123898,Human_RBP_ID_9236211,Human_RBP_ID_18427289,Human_RBP_ID_22466350 64218 RMVar_ID_64218 Human_SNP_ID_397064756 m1A Human chr9 - 34637745 34637745 34637745 GGCGGGCTCCGAGGCCGTGAGCGCAAAGCCTCAGGCCCCGGCTCCCTCCTGAGCTGCGCCGTGCC GGCGGGCTCCGAGGCCGTGAGCGCAAAGCCTCGGGCCCCGGCTCCCTCCTGAGCTGCGCCGTGCC T C SIGMAR1 Ensembl:ENSG00000147955 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1311817126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718236,Human_RBP_ID_5036139,Human_RBP_ID_5516111,Human_RBP_ID_9236211,Human_RBP_ID_18427289,Human_RBP_ID_22466350 64219 RMVar_ID_64219 Human_SNP_ID_397067579 m1A Human chr9 + 34647878 34647878 34647878 TCCACCCCTGGTCGGATGTAACGCTGCCACTCATGTCGGTCCCTGAGATCCGGGCTGTTGTTGAT TCCACCCCTGGTCGGATGTAACGCTGCCACTCGTGTCGGTCCCTGAGATCCGGGCTGTTGTTGAT A G AL162231.3,GALT Ensembl:ENSG00000258728,Ensembl:ENSG00000213930 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:34647767..34647910 26863196 MeRIP-seq:(Medium) rs111033692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5027159,Human_RBP_ID_24563588 Human_Splice_Rec_1039848,Human_Splice_Rec_1039849,Human_Splice_Rec_1039866,Human_Splice_Rec_1039867,Human_Splice_Rec_1039886,Human_Splice_Rec_1039887,Human_Splice_Rec_1039900,Human_Splice_Rec_1039907,Human_Splice_Rec_1039916,Human_Splice_Rec_1039917,Human_Splice_Rec_1039927,Human_Splice_Rec_1039936,Human_Splice_Rec_1039937,Human_Splice_Rec_1039942,Human_Splice_Rec_1039943,Human_Splice_Rec_1039967,Human_Splice_Rec_1039980,Human_Splice_Rec_1039981,Human_Splice_Rec_1040000,Human_Splice_Rec_1040001,Human_Splice_Rec_1040013,Human_Splice_Rec_1040019,Human_Splice_Rec_1040048,Human_Splice_Rec_1040049,Human_Splice_Rec_1040064,Human_Splice_Rec_1040065,Human_Splice_Rec_1040073,Human_Splice_Rec_1040094,Human_Splice_Rec_1040095 Clinvar_Rec_247 GWAS_ID_7866 RMVar_hsa_circ_4555,RMVar_hsa_circ_115911,RMVar_hsa_circ_256534 64220 RMVar_ID_64220 Human_SNP_ID_397068847 m1A Human chr9 + 34652231 34652231 34652231 AGGGCAGAGGGCGCTGGCGGCAGCGGCCGCGGAAGGTGAGGCCTGGTGTAGACGCCAAAGTCTTG AGGGCAGAGGGCGCTGGCGGCAGCGGCCGCGGTAGGTGAGGCCTGGTGTAGACGCCAAAGTCTTG A T AL162231.3,IL11RA Ensembl:ENSG00000258728,Ensembl:ENSG00000137070 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:34652188..34652260 26863196 MeRIP-seq:(Medium) rs1314956068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256672,Human_RBP_ID_26796330 Human_Splice_Rec_1040147,Human_Splice_Rec_1040169,Human_Splice_Rec_1040193 64221 RMVar_ID_64221 Human_SNP_ID_397072185 m1A Human chr9 - 34664976 34664976 34664976 TGACTCTGCCGCCGCTGTCGCCATTCGAGCCGAGCGCCCCTCCCCACACGGGCTCTGTTCCGTAC TGACTCTGCCGCCGCTGTCGCCATTCGAGCCGGGCGCCCCTCCCCACACGGGCTCTGTTCCGTAC T C AL162231.1,AL162231.4 Ensembl:ENSG00000187186,Ensembl:ENSG00000261215 Protein coding,lincRNA 3'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:34664954..34665073 26863196 MeRIP-seq:(Medium) rs953154407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3171304,Human_miRNA_ID_3172809,Human_miRNA_ID_3184650,Human_miRNA_ID_3192564,Human_miRNA_ID_3209828 64222 RMVar_ID_64222 Human_SNP_ID_397072228 m1A Human chr9 - 34665078 34665076 34665078 CCCAGCGCTCGGGTCGTGGCTTCCCCCGCCGCAGCCCCACCGCCGCTGCCCAGCCAGCCAGTGCA CCCAGCGCTCGGGTCGTGGCTTCCCCCGCCGC__CCCCACCGCCGCTGCCCAGCCAGCCAGTGCA GCT G AL162231.1,AL162231.4 Ensembl:ENSG00000187186,Ensembl:ENSG00000261215 Protein coding,lincRNA CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:34665023..34665123 32194978 MeRIP-seq:(Medium) rs372795770 Functional Loss DEL dbSNP153 33..34 33 - - - 64223 RMVar_ID_64223 Human_SNP_ID_397072578 m1A Human chr9 + 34665982 34665981 34665982 GGTGAGGATTTTCAGGGGCTGGGGTCACCTGGAGGGGGGGCTGAGAGGGGTCAGCGCAGCCTAAA GGTGAGGATTTTCAGGGGCTGGGGTCACCTGG_GGGGGGGCTGAGAGGGGTCAGCGCAGCCTAAA GA G AL162231.2 Ensembl:ENSG00000230074 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:34665616..34666006 26863196 MeRIP-seq:(Medium) rs1005779775 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5634587,Human_RBP_ID_9338890,Human_RBP_ID_16666655,Human_RBP_ID_26772644 64224 RMVar_ID_64224 Human_SNP_ID_397072593 m1A Human chr9 - 34665991 34665991 34665991 GGGCGGGAGTTTAGGCTGCGCTGACCCCTCTCAGCCCCCCCTCCAGGTGACCCCAGCCCCTGAAA GGGCGGGAGTTTAGGCTGCGCTGACCCCTCTCGGCCCCCCCTCCAGGTGACCCCAGCCCCTGAAA T C AL162231.1,AL162231.4 Ensembl:ENSG00000187186,Ensembl:ENSG00000261215 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:34665171..34678139 26863196 MeRIP-seq:(Medium) rs1483997112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036140,Human_RBP_ID_5635641 Human_Splice_Rec_1040333,Human_Splice_Rec_1040347,Human_Splice_Rec_1040355 64225 RMVar_ID_64225 Human_SNP_ID_397073417 m1A Human chr9 + 34669539 34669539 34669539 AGGAGTCCTTCTGCTTGTGTGGAGTCTGTGAGACTGTGTGTGAGGTTGGATGGGGAGAGCAAGCA AGGAGTCCTTCTGCTTGTGTGGAGTCTGTGAGTCTGTGTGTGAGGTTGGATGGGGAGAGCAAGCA A T AL162231.2 Ensembl:ENSG00000230074 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:34669496..34669615 26863196 MeRIP-seq:(Medium) rs957911677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5635186,Human_RBP_ID_24301214 64226 RMVar_ID_64226 Human_SNP_ID_397147340 m1A Human chr9 + 34989780 34989780 34989780 CCGGGTGGAGGCGGCGGAGCCGGAGCCGGGGGAGGGGGCAGCGGCTGTCTCACGGACCACGGCGG CCGGGTGGAGGCGGCGGAGCCGGAGCCGGGGGGGGGGGCAGCGGCTGTCTCACGGACCACGGCGG A G DNAJB5 Ensembl:ENSG00000137094 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34989731..34989889 26863196 MeRIP-seq:(Medium) rs910884478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1040471,Human_Splice_Rec_1040479,Human_Splice_Rec_1040485,Human_Splice_Rec_1040489,Human_Splice_Rec_1040495 64227 RMVar_ID_64227 Human_SNP_ID_397164557 m1A Human chr9 + 35057156 35057156 35057156 TACAGGTCATCATCATTGTCTTCTGTGTATACACTGCCACCTGTGCCGCCTCCACTGCCCTGACT TACAGGTCATCATCATTGTCTTCTGTGTATACGCTGCCACCTGTGCCGCCTCCACTGCCCTGACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35056970..35057224 26863196 MeRIP-seq:(Medium) rs1442790356 Functional Loss SNV dbSNP153 33..33 33 - - - 64228 RMVar_ID_64228 Human_SNP_ID_397165101 m1A Human chr9 + 35059037 35059026 35059037 TGGTGGCTGCTGCCTGGCTCTCCATGATTGGCACATCTGGGGAAAGGATGCAGACTCACCATGGC TGGTGGCTGCTGCCTGGCTCTC___________CATCTGGGGAAAGGATGCAGACTCACCATGGC CCATGATTGGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35059035..35059227 26863196 MeRIP-seq:(Medium) rs764666776 Functional Loss DEL dbSNP153 23..33 33 - - - 64229 RMVar_ID_64229 Human_SNP_ID_397165108 m1A Human chr9 + 35059037 35059037 35059037 TGGTGGCTGCTGCCTGGCTCTCCATGATTGGCACATCTGGGGAAAGGATGCAGACTCACCATGGC TGGTGGCTGCTGCCTGGCTCTCCATGATTGGCCCATCTGGGGAAAGGATGCAGACTCACCATGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35059035..35059227 26863196 MeRIP-seq:(Medium) rs1362978665 Functional Loss SNV dbSNP153 33..33 33 - - - 64230 RMVar_ID_64230 Human_SNP_ID_397165263 m1A Human chr9 + 35059610 35059610 35059610 TCAAGACGGCCAGGTCTGAGGATGGCAGGATCAATGATGTCAGGCCGGTTGGTAGCGCCAATGAT TCAAGACGGCCAGGTCTGAGGATGGCAGGATCGATGATGTCAGGCCGGTTGGTAGCGCCAATGAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35059466..35059754 26863196 MeRIP-seq:(Medium) rs777402266 Functional Loss SNV dbSNP153 33..33 33 - - - 64231 RMVar_ID_64231 Human_SNP_ID_397165296 m1A Human chr9 - 35059753 35059753 35059753 CCTGTGTGCTATTCTTTGATGAGCTGGATTCGATTGCCAAGGCTCGTGGAGGTAACATTGGAGAT CCTGTGTGCTATTCTTTGATGAGCTGGATTCGGTTGCCAAGGCTCGTGGAGGTAACATTGGAGAT T C VCP Ensembl:ENSG00000165280 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35059051..35059825 32194978 MeRIP-seq:(Medium) rs866287267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2064231,Human_RBP_ID_8928213,Human_RBP_ID_9264510,Human_RBP_ID_18908396,Human_RBP_ID_22466056,Human_RBP_ID_24301391 Human_Splice_Rec_1040572,Human_Splice_Rec_1040600,Human_Splice_Rec_1040612 Human_miRNA_ID_2132068,Human_miRNA_ID_2217667 RMVar_hsa_circ_33999,RMVar_hsa_circ_84600,RMVar_hsa_circ_326009,RMVar_hsa_circ_256539,RMVar_hsa_circ_113140,RMVar_hsa_circ_256541,RMVar_hsa_circ_102507,RMVar_hsa_circ_79819,RMVar_hsa_circ_256543,RMVar_hsa_circ_266449,RMVar_hsa_circ_256544 64232 RMVar_ID_64232 Human_SNP_ID_397166011 m1A Human chr9 + 35062330 35062330 35062330 TTTACGAAGGTTGCTCTCAGACTCACCAGCCAATTTGCTCATGATCTCAGGACCTGAAAGGATAC TTTACGAAGGTTGCTCTCAGACTCACCAGCCAGTTTGCTCATGATCTCAGGACCTGAAAGGATAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35062279..35064300 32194978 MeRIP-seq:(Medium) rs200670526 Functional Loss SNV dbSNP153 33..33 33 - - - 64233 RMVar_ID_64233 Human_SNP_ID_397168914 m1A Human chr9 - 35072177 35072177 35072177 CTAGGGGGCGAGTGAGGGGCCGTGGACCCGGCAGGCCCGGCTGGGGCCAGCTGCGCACCCGCGCG CTAGGGGGCGAGTGAGGGGCCGTGGACCCGGCGGGCCCGGCTGGGGCCAGCTGCGCACCCGCGCG T C VCP Ensembl:ENSG00000165280 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35072174..35072329 26863196 MeRIP-seq:(Medium) rs539532413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256228,Human_RBP_ID_846580,Human_RBP_ID_24555402 RMVar_hsa_circ_111680,RMVar_hsa_circ_256545 64234 RMVar_ID_64234 Human_SNP_ID_397169036 m1A Human chr9 + 35072449 35072449 35072449 AGCGACCGACTGGGCCGGGGCTCGGCTCTTCCAGGCGGTGGGCGAGCAGCGGCGACAAACCCGCA AGCGACCGACTGGGCCGGGGCTCGGCTCTTCCGGGCGGTGGGCGAGCAGCGGCGACAAACCCGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35072403..35072625 26863196 MeRIP-seq:(Medium) rs1009048936 Functional Loss SNV dbSNP153 33..33 33 - - - 64235 RMVar_ID_64235 Human_SNP_ID_397169755 m1A Human chr9 - 35074977 35074977 35074977 TAGTCGTGGACTGGAATGGGTAGCCAGCGGCCAGGATACCAAAGCCTTACAGGACTTCCTCCTCA TAGTCGTGGACTGGAATGGGTAGCCAGCGGCCGGGATACCAAAGCCTTACAGGACTTCCTCCTCA T C FANCG Ensembl:ENSG00000221829 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35074889..35075012 26863196 MeRIP-seq:(Medium) rs1416054222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18135492 Human_Splice_Rec_1040651,Human_Splice_Rec_1040679 RMVar_hsa_circ_82931,RMVar_hsa_circ_94712,RMVar_hsa_circ_119528,RMVar_hsa_circ_256550,RMVar_hsa_circ_256551,RMVar_hsa_circ_103352,RMVar_hsa_circ_256552,RMVar_hsa_circ_256553 64236 RMVar_ID_64236 Human_SNP_ID_397170008 m1A Human chr9 + 35075724 35075724 35075724 TACCGCTGCCTCCAAAAACACCTCAGGCATACAGGGCCCTGGAGGGGAGGGGGGTGGGGAGAACT TACCGCTGCCTCCAAAAACACCTCAGGCATACGGGGCCCTGGAGGGGAGGGGGGTGGGGAGAACT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35075676..35075750 32194978 MeRIP-seq:(Medium) rs760449357 Functional Loss SNV dbSNP153 33..33 33 - - - 64237 RMVar_ID_64237 Human_SNP_ID_397170300 m1A Human chr9 - 35076585 35076585 35076585 GATTATAGATACAATTTTTTTCTTTCTCTTTTAGGCCTTGAATGTCCCATGCAGTTCCAAAGCCC GATTATAGATACAATTTTTTTCTTTCTCTTTTGGGCCTTGAATGTCCCATGCAGTTCCAAAGCCC T C FANCG Ensembl:ENSG00000221829 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35076551..35076600 32194978 MeRIP-seq:(Medium) rs397507561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7924218 Clinvar_Rec_248 RMVar_hsa_circ_82931,RMVar_hsa_circ_36773,RMVar_hsa_circ_256551,RMVar_hsa_circ_31330,RMVar_hsa_circ_87205,RMVar_hsa_circ_256554 64238 RMVar_ID_64238 Human_SNP_ID_397175896 m1A Human chr9 - 35095413 35095413 35095413 TGCCAAGAGCCCCCAGGCCCTGGGTCCCTGCCATGGGGGAGCCAAGGGAAACCTGGGGCCTGCTG TGCCAAGAGCCCCCAGGCCCTGGGTCCCTGCCGTGGGGGAGCCAAGGGAAACCTGGGGCCTGCTG T C PIGO Ensembl:ENSG00000165282 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:35095392..35095552 26863196 MeRIP-seq:(Medium) rs758429983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5042594,Human_RBP_ID_18135533,Human_RBP_ID_22466370,Human_RBP_ID_26221932 RMVar_hsa_circ_107327,RMVar_hsa_circ_256561 64239 RMVar_ID_64239 Human_SNP_ID_397177403 m1A Human chr9 - 35100968 35100968 35100968 GCAGTTCTGGCGAAGGCCAAGGCTAAAGCTGAAGCTATTCGAATCCTGGCTGCAGCTCTGACACA GCAGTTCTGGCGAAGGCCAAGGCTAAAGCTGAGGCTATTCGAATCCTGGCTGCAGCTCTGACACA T C STOML2 Ensembl:ENSG00000165283 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs943535991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718368 Human_Splice_Rec_1040806,Human_Splice_Rec_1040807,Human_Splice_Rec_1040822,Human_Splice_Rec_1040823,Human_Splice_Rec_1040840,Human_Splice_Rec_1040841,Human_Splice_Rec_1040848 RMVar_hsa_circ_75983,RMVar_hsa_circ_118449,RMVar_hsa_circ_87515,RMVar_hsa_circ_111866,RMVar_hsa_circ_86444,RMVar_hsa_circ_256563,RMVar_hsa_circ_256565,RMVar_hsa_circ_256566,RMVar_hsa_circ_256564,RMVar_hsa_circ_256562 64240 RMVar_ID_64240 Human_SNP_ID_397177540 m1A Human chr9 - 35101403 35101394 35101404 GCAGATGCAGGTGGGGGCCAAGGAGGGGTGGGAAAAGGGCCTCAGGGTGCTCCAGTACCAGGAGG GCAGATGCAGGTGGGGGCCAAGGAGGGGTGG__________TCAGGGTGCTCCAGTACCAGGAGG AGGCCCTTTTC A STOML2 Ensembl:ENSG00000165283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35101401..35101519 26863196 MeRIP-seq:(Medium) rs776528307 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_19143341 RMVar_hsa_circ_75983,RMVar_hsa_circ_118449,RMVar_hsa_circ_111866,RMVar_hsa_circ_86444,RMVar_hsa_circ_27307,RMVar_hsa_circ_256563,RMVar_hsa_circ_256565,RMVar_hsa_circ_256564,RMVar_hsa_circ_256562 64241 RMVar_ID_64241 Human_SNP_ID_397177543 m1A Human chr9 - 35101403 35101403 35101403 GCAGATGCAGGTGGGGGCCAAGGAGGGGTGGGAAAAGGGCCTCAGGGTGCTCCAGTACCAGGAGG GCAGATGCAGGTGGGGGCCAAGGAGGGGTGGGCAAAGGGCCTCAGGGTGCTCCAGTACCAGGAGG T G STOML2 Ensembl:ENSG00000165283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35101401..35101519 26863196 MeRIP-seq:(Medium) rs774958844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19143341 RMVar_hsa_circ_75983,RMVar_hsa_circ_118449,RMVar_hsa_circ_111866,RMVar_hsa_circ_86444,RMVar_hsa_circ_27307,RMVar_hsa_circ_256563,RMVar_hsa_circ_256565,RMVar_hsa_circ_256564,RMVar_hsa_circ_256562 64242 RMVar_ID_64242 Human_SNP_ID_397177811 m1A Human chr9 - 35102161 35102161 35102161 GTTTGAACATCCTCATCCCTGTGTTAGACCGGATCCGATATGTGCAGAGTCTCAAGGAAATTGTC GTTTGAACATCCTCATCCCTGTGTTAGACCGGGTCCGATATGTGCAGAGTCTCAAGGAAATTGTC T C STOML2 Ensembl:ENSG00000165283 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35102084..35102216 26863196 MeRIP-seq:(Medium) rs773757788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718392,Human_RBP_ID_1059219,Human_RBP_ID_1705134,Human_RBP_ID_2064298,Human_RBP_ID_8704162,Human_RBP_ID_16668174,Human_RBP_ID_18908481,Human_RBP_ID_22466813,Human_RBP_ID_23141629,Human_RBP_ID_24301532 Human_Splice_Rec_1040798,Human_Splice_Rec_1040799,Human_Splice_Rec_1040812,Human_Splice_Rec_1040813,Human_Splice_Rec_1040830,Human_Splice_Rec_1040831,Human_Splice_Rec_1040851 Human_miRNA_ID_1983379 RMVar_hsa_circ_75983,RMVar_hsa_circ_118449,RMVar_hsa_circ_86444,RMVar_hsa_circ_256563,RMVar_hsa_circ_256564,RMVar_hsa_circ_256562,RMVar_hsa_circ_32763 64243 RMVar_ID_64243 Human_SNP_ID_397177968 m1A Human chr9 + 35102756 35102745 35102757 CCACCCAGGCCTCCTGCTGCGGCACGAACAGTACCACGGTGTTTCGGGGCAATCCAGAGGAGGCG CCACCCAGGCCTCCTGCTGCGG____________CACGGTGTTTCGGGGCAATCCAGAGGAGGCG GCACGAACAGTAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:35102706..35102898 26863196 MeRIP-seq:(Medium) rs752109773 Functional Loss DEL dbSNP153 23..34 33 - - - 64244 RMVar_ID_64244 Human_SNP_ID_397177978 m1A Human chr9 + 35102759 35102759 35102759 CCCAGGCCTCCTGCTGCGGCACGAACAGTACCACGGTGTTTCGGGGCAATCCAGAGGAGGCGCGG CCCAGGCCTCCTGCTGCGGCACGAACAGTACCGCGGTGTTTCGGGGCAATCCAGAGGAGGCGCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35102644..35102829 26863196 MeRIP-seq:(Medium) rs1263884907 Functional Loss SNV dbSNP153 33..33 33 - - - 64245 RMVar_ID_64245 Human_SNP_ID_397178104 m1A Human chr9 + 35103100 35103100 35103100 AGTGCCCCGCGCCGCGCGCGCCAGCATTTCCCACCGCCGCAGCGACCTCCGGAACCAACGAGACG AGTGCCCCGCGCCGCGCGCGCCAGCATTTCCCCCCGCCGCAGCGACCTCCGGAACCAACGAGACG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:35102992..35103156;chr9:35102987..35103150;chr9:35102982..35103125 26863196 MeRIP-seq:(Medium) rs745615531 Functional Loss SNV dbSNP153 33..33 33 - - - 64246 RMVar_ID_64246 Human_SNP_ID_397193038 m1A Human chr9 + 35162201 35162201 35162201 GGAGCTGCCAGACCCGTGGGGCCGGTAACGAGAGCAGTCGCGGCACCTGCTGAGAGGAAAGAGGG GGAGCTGCCAGACCCGTGGGGCCGGTAACGAGGGCAGTCGCGGCACCTGCTGAGAGGAAAGAGGG A G UNC13B Ensembl:ENSG00000198722 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:35162014..35162297 26863196 MeRIP-seq:(Medium) rs910211063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256929,Human_RBP_ID_5535328,Human_RBP_ID_8944616 64247 RMVar_ID_64247 Human_SNP_ID_397242198 m1A Human chr9 - 35380636 35380636 35380636 AGCAACTTTCTCGGGTCCAGTTTCCTCACCCAAGTTGTACCAGACGTCCATCTCGCCACTTAGGG AGCAACTTTCTCGGGTCCAGTTTCCTCACCCAGGTTGTACCAGACGTCCATCTCGCCACTTAGGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35380606..35381557 32194978 MeRIP-seq:(Medium) rs773244745 Functional Loss SNV dbSNP153 33..33 33 - - - 64248 RMVar_ID_64248 Human_SNP_ID_397242475 m1A Human chr9 - 35381706 35381706 35381706 TGCCGCAGCAGAGACTCACGTCATGGCCTGATATATGGACTCAATGCCATAACGCATGGCAAATT TGCCGCAGCAGAGACTCACGTCATGGCCTGATTTATGGACTCAATGCCATAACGCATGGCAAATT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35381655..35382393 32194978 MeRIP-seq:(Medium) rs756611040 Functional Loss SNV dbSNP153 33..33 33 - - - 64249 RMVar_ID_64249 Human_SNP_ID_397243548 m1A Human chr9 + 35386289 35386289 35386289 CAACTGCCACGACTTATACAGCCGCCAGTACCAGCTGGTAAGAGGTTCAGGATCAGGTGGGGCCA CAACTGCCACGACTTATACAGCCGCCAGTACCGGCTGGTAAGAGGTTCAGGATCAGGTGGGGCCA A G UNC13B Ensembl:ENSG00000198722 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35386240..35389892 32194978 MeRIP-seq:(Medium) rs778676265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1041015,Human_Splice_Rec_1041095,Human_Splice_Rec_1041175,Human_Splice_Rec_1041253,Human_Splice_Rec_1041329,Human_Splice_Rec_1041409,Human_Splice_Rec_1041487,Human_Splice_Rec_1041557,Human_Splice_Rec_1041619 RMVar_hsa_circ_94915,RMVar_hsa_circ_256575,RMVar_hsa_circ_85402,RMVar_hsa_circ_256581,RMVar_hsa_circ_92399,RMVar_hsa_circ_116513,RMVar_hsa_circ_123983,RMVar_hsa_circ_113740,RMVar_hsa_circ_90052,RMVar_hsa_circ_91118,RMVar_hsa_circ_256582,RMVar_hsa_circ_256586,RMVar_hsa_circ_256587,RMVar_hsa_circ_256584,RMVar_hsa_circ_256585,RMVar_hsa_circ_256583,RMVar_hsa_circ_77910,RMVar_hsa_circ_29907,RMVar_hsa_circ_256595 64250 RMVar_ID_64250 Human_SNP_ID_397265944 m1A Human chr9 - 35489920 35489920 35489920 AGGTGCTCGCCCCCTCCCCGGCTCCCGCAGCGATGGGCGCAGCCGAGTCACGCGCAGAGCTTTCC AGGTGCTCGCCCCCTCCCCGGCTCCCGCAGCGCTGGGCGCAGCCGAGTCACGCGCAGAGCTTTCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:35489874..35490429 26863196 MeRIP-seq:(Medium) rs1403521480 Functional Loss SNV dbSNP153 33..33 33 - - - 64251 RMVar_ID_64251 Human_SNP_ID_397278703 m1A Human chr9 - 35546752 35546752 35546752 CTCCTACTCTTGGTGCTGTCTATAGACCGTGCAGTTCCTCCTGGAGTAGAGTGCAGGCTGCTGAA CTCCTACTCTTGGTGCTGTCTATAGACCGTGCGGTTCCTCCTGGAGTAGAGTGCAGGCTGCTGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35546703..35546804 32194978 MeRIP-seq:(Medium) rs1048647344 Functional Loss SNV dbSNP153 33..33 33 - - - 64252 RMVar_ID_64252 Human_SNP_ID_397279370 m1A Human chr9 + 35548497 35548497 35548497 TCCAGGGCCTGCTCTCCCAGGGAGCCCAGCCAACAGCCATACCCAGAGGGATGCAAGAGCTAGAG TCCAGGGCCTGCTCTCCCAGGGAGCCCAGCCACCAGCCATACCCAGAGGGATGCAAGAGCTAGAG A C RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35548447..35555072 32194978 MeRIP-seq:(Medium) rs748624347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1041795,Human_Splice_Rec_1041817 RMVar_hsa_circ_30644,RMVar_hsa_circ_108460,RMVar_hsa_circ_99209,RMVar_hsa_circ_300904,RMVar_hsa_circ_256601,RMVar_hsa_circ_289737,RMVar_hsa_circ_84946,RMVar_hsa_circ_256602,RMVar_hsa_circ_256603,RMVar_hsa_circ_256604 64253 RMVar_ID_64253 Human_SNP_ID_397280951 m1A Human chr9 + 35555392 35555392 35555392 CTCGGCCATCGCCCCTGGGCAGCTACTCCCCCATCCGGAGTGTTGGCCCCTTTGGGCCCAGCACT CTCGGCCATCGCCCCTGGGCAGCTACTCCCCCTTCCGGAGTGTTGGCCCCTTTGGGCCCAGCACT A T RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:35555351..35555510 26863196 MeRIP-seq:(Medium) rs1424286148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17322134 RMVar_hsa_circ_30644,RMVar_hsa_circ_99209,RMVar_hsa_circ_300904,RMVar_hsa_circ_84946,RMVar_hsa_circ_27510,RMVar_hsa_circ_256603,RMVar_hsa_circ_256604,RMVar_hsa_circ_93503,RMVar_hsa_circ_325006,RMVar_hsa_circ_256605,RMVar_hsa_circ_23327,RMVar_hsa_circ_256606 64254 RMVar_ID_64254 Human_SNP_ID_397282357 m1A Human chr9 + 35560357 35560351 35560357 GTGAAGGGTGTGGGTGCCTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGAGGAGACAGAAGAGGT GTGAAGGGTGTGGGTGCCTCAGAAGGT______GAGGAAGAGGAAGAAGAGGAGACAGAAGAGGT TGGAGAA T RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:35560183..35560724;chr9:35560034..35560628 26863196 MeRIP-seq:(Medium) rs770794085 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_15303,Human_RBP_ID_219649,Human_RBP_ID_963129,Human_RBP_ID_3974469,Human_RBP_ID_26361685 RMVar_hsa_circ_30644,RMVar_hsa_circ_27510,RMVar_hsa_circ_67936 64255 RMVar_ID_64255 Human_SNP_ID_397282369 m1A Human chr9 + 35560374 35560372 35560375 CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGAGGAGACAGAAGAGGTGGCAGAGGCAGCCGGGG CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAA___GAGACAGAAGAGGTGGCAGAGGCAGCCGGGG AGAG A RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35560176..35560764 26863196 MeRIP-seq:(Medium) rs761868077 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_15303,Human_RBP_ID_219649,Human_RBP_ID_963129,Human_RBP_ID_3974469,Human_RBP_ID_19023793,Human_RBP_ID_26361685 RMVar_hsa_circ_30644,RMVar_hsa_circ_27510,RMVar_hsa_circ_67936 64256 RMVar_ID_64256 Human_SNP_ID_397282371 m1A Human chr9 + 35560374 35560374 35560374 CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGAGGAGACAGAAGAGGTGGCAGAGGCAGCCGGGG CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGGGGAGACAGAAGAGGTGGCAGAGGCAGCCGGGG A G RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35560176..35560764 26863196 MeRIP-seq:(Medium) rs1322624320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15303,Human_RBP_ID_219649,Human_RBP_ID_963129,Human_RBP_ID_3974469,Human_RBP_ID_19023793,Human_RBP_ID_26361685 RMVar_hsa_circ_30644,RMVar_hsa_circ_27510,RMVar_hsa_circ_67936 64257 RMVar_ID_64257 Human_SNP_ID_397282674 m1A Human chr9 + 35561087 35561087 35561087 TGCAGGAGCCACACTCCCCAGCCCTGCCCTCCAGTCCTCCGTGGTAAGCCTGGGGAAACGGAAGG TGCAGGAGCCACACTCCCCAGCCCTGCCCTCCGGTCCTCCGTGGTAAGCCTGGGGAAACGGAAGG A G RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35560610..35561450 32194978 MeRIP-seq:(Medium) rs762110912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1041813,Human_Splice_Rec_1041835 RMVar_hsa_circ_30644,RMVar_hsa_circ_27510,RMVar_hsa_circ_67936 64258 RMVar_ID_64258 Human_SNP_ID_397282801 m1A Human chr9 - 35561338 35561338 35561338 GCTTCCAGGGGTTGGACTTGGAGTTGGGGTCAATGTCACGTAGGCCAGGGGCACCAGGCCAGAGT GCTTCCAGGGGTTGGACTTGGAGTTGGGGTCAGTGTCACGTAGGCCAGGGGCACCAGGCCAGAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:35561288..35561387 26863196 MeRIP-seq:(Medium) rs773985044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256613 64259 RMVar_ID_64259 Human_SNP_ID_397293970 m1A Human chr9 + 35605712 35605691 35605712 GAGGGGCCCCCGGGGCCGGGGGGCACGGGCGGAGGCCCGGGCCGGGGCCGCCCCTCCTCCTACCG GAGGGGCCCCCG_____________________GGCCCGGGCCGGGGCCGCCCCTCCTCCTACCG GGGGCCGGGGGGCACGGGCGGA G TESK1 Ensembl:ENSG00000107140 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35605664..35605756 26863196 MeRIP-seq:(Medium) rs1303881202 Functional Loss DEL dbSNP153 13..33 33 - - - 64260 RMVar_ID_64260 Human_SNP_ID_397307437 m1A Human chr9 - 35657804 35657804 35657804 GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCAGGCAGTGCGTGTCCGCGCACCAACCACACGGG GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCTGGCAGTGCGTGTCCGCGCACCAACCACACGGG T A RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35657751..35657991 26863196 MeRIP-seq:(Medium) rs886041234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287122,Human_RBP_ID_718450,Human_RBP_ID_1227303,Human_RBP_ID_1705179,Human_RBP_ID_3213000,Human_RBP_ID_3911352,Human_RBP_ID_5027726,Human_RBP_ID_5091043,Human_RBP_ID_5107165,Human_RBP_ID_5251765,Human_RBP_ID_5634106,Human_RBP_ID_5641201,Human_RBP_ID_5659164,Human_RBP_ID_7924749,Human_RBP_ID_8158311,Human_RBP_ID_8226240,Human_RBP_ID_8275237,Human_RBP_ID_8704239,Human_RBP_ID_8928295,Human_RBP_ID_9236318,Human_RBP_ID_16668953,Human_RBP_ID_17056208,Human_RBP_ID_17065640,Human_RBP_ID_17549648,Human_RBP_ID_17716556,Human_RBP_ID_18135616,Human_RBP_ID_18203401,Human_RBP_ID_18212273,Human_RBP_ID_18453543,Human_RBP_ID_18908530,Human_RBP_ID_21723957,Human_RBP_ID_21955631,Human_RBP_ID_22340120,Human_RBP_ID_22838648,Human_RBP_ID_23092421,Human_RBP_ID_23141632,Human_RBP_ID_23201295,Human_RBP_ID_24301863,Human_RBP_ID_24523633,Human_RBP_ID_26222159,Human_RBP_ID_26563623,Human_RBP_ID_26752284,Human_RBP_ID_27136347,Human_RBP_ID_27162470,Human_RBP_ID_27375103,Human_RBP_ID_27545942,Human_RBP_ID_27570589 RMVar_hsa_circ_256617,RMVar_hsa_circ_269876 64261 RMVar_ID_64261 Human_SNP_ID_397307438 m1A Human chr9 - 35657804 35657804 35657804 GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCAGGCAGTGCGTGTCCGCGCACCAACCACACGGG GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCGGGCAGTGCGTGTCCGCGCACCAACCACACGGG T C RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35657751..35657991 26863196 MeRIP-seq:(Medium) rs886041234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287122,Human_RBP_ID_718450,Human_RBP_ID_1227303,Human_RBP_ID_1705179,Human_RBP_ID_3213000,Human_RBP_ID_3911352,Human_RBP_ID_5027726,Human_RBP_ID_5091043,Human_RBP_ID_5107165,Human_RBP_ID_5251765,Human_RBP_ID_5634106,Human_RBP_ID_5641201,Human_RBP_ID_5659164,Human_RBP_ID_7924749,Human_RBP_ID_8158311,Human_RBP_ID_8226240,Human_RBP_ID_8275237,Human_RBP_ID_8704239,Human_RBP_ID_8928295,Human_RBP_ID_9236318,Human_RBP_ID_16668953,Human_RBP_ID_17056208,Human_RBP_ID_17065640,Human_RBP_ID_17549648,Human_RBP_ID_17716556,Human_RBP_ID_18135616,Human_RBP_ID_18203401,Human_RBP_ID_18212273,Human_RBP_ID_18453543,Human_RBP_ID_18908530,Human_RBP_ID_21723957,Human_RBP_ID_21955631,Human_RBP_ID_22340120,Human_RBP_ID_22838648,Human_RBP_ID_23092421,Human_RBP_ID_23141632,Human_RBP_ID_23201295,Human_RBP_ID_24301863,Human_RBP_ID_24523633,Human_RBP_ID_26222159,Human_RBP_ID_26563623,Human_RBP_ID_26752284,Human_RBP_ID_27136347,Human_RBP_ID_27162470,Human_RBP_ID_27375103,Human_RBP_ID_27545942,Human_RBP_ID_27570589 RMVar_hsa_circ_256617,RMVar_hsa_circ_269876 64262 RMVar_ID_64262 Human_SNP_ID_397307439 m1A Human chr9 - 35657804 35657804 35657804 GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCAGGCAGTGCGTGTCCGCGCACCAACCACACGGG GGGCGTCATCCGTCAGCTCCCTCTAGTTACGCCGGCAGTGCGTGTCCGCGCACCAACCACACGGG T G RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35657751..35657991 26863196 MeRIP-seq:(Medium) rs886041234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287122,Human_RBP_ID_718450,Human_RBP_ID_1227303,Human_RBP_ID_1705179,Human_RBP_ID_3213000,Human_RBP_ID_3911352,Human_RBP_ID_5027726,Human_RBP_ID_5091043,Human_RBP_ID_5107165,Human_RBP_ID_5251765,Human_RBP_ID_5634106,Human_RBP_ID_5641201,Human_RBP_ID_5659164,Human_RBP_ID_7924749,Human_RBP_ID_8158311,Human_RBP_ID_8226240,Human_RBP_ID_8275237,Human_RBP_ID_8704239,Human_RBP_ID_8928295,Human_RBP_ID_9236318,Human_RBP_ID_16668953,Human_RBP_ID_17056208,Human_RBP_ID_17065640,Human_RBP_ID_17549648,Human_RBP_ID_17716556,Human_RBP_ID_18135616,Human_RBP_ID_18203401,Human_RBP_ID_18212273,Human_RBP_ID_18453543,Human_RBP_ID_18908530,Human_RBP_ID_21723957,Human_RBP_ID_21955631,Human_RBP_ID_22340120,Human_RBP_ID_22838648,Human_RBP_ID_23092421,Human_RBP_ID_23141632,Human_RBP_ID_23201295,Human_RBP_ID_24301863,Human_RBP_ID_24523633,Human_RBP_ID_26222159,Human_RBP_ID_26563623,Human_RBP_ID_26752284,Human_RBP_ID_27136347,Human_RBP_ID_27162470,Human_RBP_ID_27375103,Human_RBP_ID_27545942,Human_RBP_ID_27570589 RMVar_hsa_circ_256617,RMVar_hsa_circ_269876 64263 RMVar_ID_64263 Human_SNP_ID_397307519 m1A Human chr9 + 35657853 35657853 35657853 CTGACGGATGACGCCCCCGCGCCACGCCGCTCAGCGGGATACGCTTCTTGGCGGACTTTGGAGTG CTGACGGATGACGCCCCCGCGCCACGCCGCTCCGCGGGATACGCTTCTTGGCGGACTTTGGAGTG A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:35657806..35657943;chr9:35657806..35657941 26863196 MeRIP-seq:(Medium) rs1160309777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256618,RMVar_hsa_circ_256620,RMVar_hsa_circ_256621,RMVar_hsa_circ_256623 64264 RMVar_ID_64264 Human_SNP_ID_397307520 m1A Human chr9 + 35657853 35657853 35657853 CTGACGGATGACGCCCCCGCGCCACGCCGCTCAGCGGGATACGCTTCTTGGCGGACTTTGGAGTG CTGACGGATGACGCCCCCGCGCCACGCCGCTCGGCGGGATACGCTTCTTGGCGGACTTTGGAGTG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:35657806..35657943;chr9:35657806..35657941 26863196 MeRIP-seq:(Medium) rs1160309777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256618,RMVar_hsa_circ_256620,RMVar_hsa_circ_256621,RMVar_hsa_circ_256623 64265 RMVar_ID_64265 Human_SNP_ID_397307529 m1A Human chr9 + 35657859 35657859 35657859 GATGACGCCCCCGCGCCACGCCGCTCAGCGGGATACGCTTCTTGGCGGACTTTGGAGTGGGAAGC GATGACGCCCCCGCGCCACGCCGCTCAGCGGGCTACGCTTCTTGGCGGACTTTGGAGTGGGAAGC A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:35657758..35658001 26863196 MeRIP-seq:(Medium) rs754810221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256618,RMVar_hsa_circ_256620,RMVar_hsa_circ_256621,RMVar_hsa_circ_256623 64266 RMVar_ID_64266 Human_SNP_ID_397307530 m1A Human chr9 + 35657859 35657859 35657859 GATGACGCCCCCGCGCCACGCCGCTCAGCGGGATACGCTTCTTGGCGGACTTTGGAGTGGGAAGC GATGACGCCCCCGCGCCACGCCGCTCAGCGGGGTACGCTTCTTGGCGGACTTTGGAGTGGGAAGC A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:35657758..35658001 26863196 MeRIP-seq:(Medium) rs754810221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256618,RMVar_hsa_circ_256620,RMVar_hsa_circ_256621,RMVar_hsa_circ_256623 64267 RMVar_ID_64267 Human_SNP_ID_397307614 m1A Human chr9 - 35657906 35657906 35657906 GACCTCGGGCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAAAGTC GACCTCGGGCAGAGAGTGCCACGTGCATACGCGCGTAGACATTCCCCGCTTCCCACTCCAAAGTC T C RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:35657761..35658002 26863196 MeRIP-seq:(Medium) rs772825736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256956,Human_RBP_ID_271138,Human_RBP_ID_287319,Human_RBP_ID_718454,Human_RBP_ID_798268,Human_RBP_ID_846511,Human_RBP_ID_964456,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1339058,Human_RBP_ID_1705183,Human_RBP_ID_2064328,Human_RBP_ID_3232116,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5091045,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5536152,Human_RBP_ID_7924755,Human_RBP_ID_8160933,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928298,Human_RBP_ID_9236322,Human_RBP_ID_16668969,Human_RBP_ID_17056210,Human_RBP_ID_17065642,Human_RBP_ID_17174832,Human_RBP_ID_17201973,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135622,Human_RBP_ID_18203406,Human_RBP_ID_18212282,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908535,Human_RBP_ID_21723960,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23095275,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316705,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563628,Human_RBP_ID_26738292,Human_RBP_ID_26752291,Human_RBP_ID_27136347,Human_RBP_ID_27162478,Human_RBP_ID_27545947,Human_RBP_ID_27570593 Human_miRNA_ID_3146022,Human_miRNA_ID_3161294,Human_miRNA_ID_3205215 RMVar_hsa_circ_256617,RMVar_hsa_circ_269876,RMVar_hsa_circ_256622 64268 RMVar_ID_64268 Human_SNP_ID_397307620 m1A Human chr9 - 35657910 35657910 35657910 CCCGGACCTCGGGCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAA CCCGGACCTCGGGCAGAGAGTGCCACGTGCATGCGCACGTAGACATTCCCCGCTTCCCACTCCAA T C RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr9:35657756..35658011;chr9:35657758..35658012 26863196 MeRIP-seq:(Medium) rs567665484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256956,Human_RBP_ID_271138,Human_RBP_ID_287319,Human_RBP_ID_718454,Human_RBP_ID_798268,Human_RBP_ID_846511,Human_RBP_ID_964456,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1705183,Human_RBP_ID_2064328,Human_RBP_ID_3232116,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5091045,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5536152,Human_RBP_ID_5659166,Human_RBP_ID_7924755,Human_RBP_ID_8160933,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928298,Human_RBP_ID_9236322,Human_RBP_ID_16668969,Human_RBP_ID_17056210,Human_RBP_ID_17065642,Human_RBP_ID_17174832,Human_RBP_ID_17201973,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135622,Human_RBP_ID_18203406,Human_RBP_ID_18212282,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908535,Human_RBP_ID_21723960,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23095275,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316705,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563628,Human_RBP_ID_26738292,Human_RBP_ID_26752291,Human_RBP_ID_27136347,Human_RBP_ID_27162478,Human_RBP_ID_27545947,Human_RBP_ID_27570593 Human_miRNA_ID_3146022,Human_miRNA_ID_3161294,Human_miRNA_ID_3205215 RMVar_hsa_circ_256617,RMVar_hsa_circ_269876,RMVar_hsa_circ_256622 64269 RMVar_ID_64269 Human_SNP_ID_397307670 m1A Human chr9 + 35657934 35657934 35657934 TACGTGCGTATGCACGTGGCACTCTCTGCCCGAGGTCCGGGGACTTTCCCCTAGGCGGAAAGGGG TACGTGCGTATGCACGTGGCACTCTCTGCCCGCGGTCCGGGGACTTTCCCCTAGGCGGAAAGGGG A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35657776..35657975 32194978 MeRIP-seq:(Medium) rs991322091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256620,RMVar_hsa_circ_256621,RMVar_hsa_circ_256623 64270 RMVar_ID_64270 Human_SNP_ID_397307727 m1A Human chr9 + 35657967 35657967 35657967 GGTCCGGGGACTTTCCCCTAGGCGGAAAGGGGAGGAACAGAGTCCTCAGTGTGTAGCCTAGGATA GGTCCGGGGACTTTCCCCTAGGCGGAAAGGGGGGGAACAGAGTCCTCAGTGTGTAGCCTAGGATA A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:35657779..35658010 26863196 MeRIP-seq:(Medium) rs1241779282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1962021,Human_miRNA_ID_1962022 RMVar_hsa_circ_86880,RMVar_hsa_circ_256619,RMVar_hsa_circ_103296,RMVar_hsa_circ_256621 64271 RMVar_ID_64271 Human_SNP_ID_397309121 m1A Human chr9 - 35661055 35661055 35661055 CTCCGTAGTCCCCGCCCCACCTCCCAGGAAGTAGCTAGGTTCCATGTCTCTGTGCTCCAGTTTGT CTCCGTAGTCCCCGCCCCACCTCCCAGGAAGTGGCTAGGTTCCATGTCTCTGTGCTCCAGTTTGT T C ARHGEF39 Ensembl:ENSG00000137135 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:35661004..35661133 26863196 MeRIP-seq:(Medium) rs1470245106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27136358 64272 RMVar_ID_64272 Human_SNP_ID_397310433 m1A Human chr9 + 35665135 35665135 35665135 GTTTCCGCTCCCAGCGGGCACGCTGCTCTTGCACCGGGCACCGCGAACCGGGGCAGGAGAGCTCC GTTTCCGCTCCCAGCGGGCACGCTGCTCTTGCGCCGGGCACCGCGAACCGGGGCAGGAGAGCTCC A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:35664952..35665140 26863196 MeRIP-seq:(Medium) rs1393297091 Functional Loss SNV dbSNP153 33..33 33 - - - 64273 RMVar_ID_64273 Human_SNP_ID_397312566 m1A Human chr9 - 35673970 35673970 35673970 GGATCAACAGAGGGAGCCAGGGGCTGGGGCACAGGGGAGCCATGCGGCTGACTGTGGGGTGTCCC GGATCAACAGAGGGAGCCAGGGGCTGGGGCACGGGGGAGCCATGCGGCTGACTGTGGGGTGTCCC T C ARHGEF39 Ensembl:ENSG00000137135 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:35673950..35674067 26863196 MeRIP-seq:(Medium) rs1177505640 Functional Loss SNV dbSNP153 33..33 33 - - - 64274 RMVar_ID_64274 Human_SNP_ID_397312575 m1A Human chr9 - 35673996 35673996 35673996 CACAGTGAGGCCTGGAGCAGGGGCCGGGATCAACAGAGGGAGCCAGGGGCTGGGGCACAGGGGAG CACAGTGAGGCCTGGAGCAGGGGCCGGGATCACCAGAGGGAGCCAGGGGCTGGGGCACAGGGGAG T G ARHGEF39 Ensembl:ENSG00000137135 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35673948..35674056 26863196 MeRIP-seq:(Medium) rs1374982001 Functional Loss SNV dbSNP153 33..33 33 - - - 64275 RMVar_ID_64275 Human_SNP_ID_397314786 m1A Human chr9 - 35681082 35681082 35681082 GGAAGTGGCATAATGAGCAGGACAGGACAGTTACCGGCTCCCCCTCAGATGCCTCTGGCTGGCTT GGAAGTGGCATAATGAGCAGGACAGGACAGTTGCCGGCTCCCCCTCAGATGCCTCTGGCTGGCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35681076..35681100 32194978 MeRIP-seq:(Medium) rs1278535787 Functional Loss SNV dbSNP153 33..33 33 - - - 64276 RMVar_ID_64276 Human_SNP_ID_397315039 m1A Human chr9 - 35682063 35682063 35682063 CTCAACAACCTGTGAGGGCCAGCCCCACCCCCAGCCAGGCTATGGTTGCCACCCCAACCCAATAA CTCAACAACCTGTGAGGGCCAGCCCCACCCCCTGCCAGGCTATGGTTGCCACCCCAACCCAATAA T A TPM2 Ensembl:ENSG00000198467 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:35682001..35682452;chr9:35682001..35682303 26863196 MeRIP-seq:(Medium) rs754945031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92183,Human_RBP_ID_9407998,Human_RBP_ID_18173431,Human_RBP_ID_19024951,Human_RBP_ID_26361686,Human_RBP_ID_27545966,Human_RBP_ID_27833044 Human_miRNA_ID_795872,Human_miRNA_ID_1361009,Human_miRNA_ID_2331522,Human_miRNA_ID_2684296,Human_miRNA_ID_2964605 RMVar_hsa_circ_256626,RMVar_hsa_circ_80855 64277 RMVar_ID_64277 Human_SNP_ID_397315264 m1A Human chr9 + 35682793 35682793 35682793 ACAGCCAGGGAGTGCCTGTGCAGAGGGGTTTCAGCGTGGGCCATGGTGTTTTGTGGGTGGGCTCA ACAGCCAGGGAGTGCCTGTGCAGAGGGGTTTCGGCGTGGGCCATGGTGTTTTGTGGGTGGGCTCA A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35682790..35682891 32194978 MeRIP-seq:(Medium) rs982242863 Functional Loss SNV dbSNP153 33..33 33 - - - 64278 RMVar_ID_64278 Human_SNP_ID_397315353 m1A Human chr9 + 35683117 35683113 35683118 CTGCTCCCCTCCCCATAGAGAGAATGGAAAGGAGAGGAGAGAAGAGAGCTGAGGTGGCCACGCTG CTGCTCCCCTCCCCATAGAGAGAATGGAA_____AGGAGAGAAGAGAGCTGAGGTGGCCACGCTG AAGGAG A RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35683115..35683216 32194978 MeRIP-seq:(Medium) rs747936701 Functional Loss DEL dbSNP153 30..34 33 - - - 64279 RMVar_ID_64279 Human_SNP_ID_397315869 m1A Human chr9 + 35684801 35684801 35684801 GTAACAATTTTCAGCTCCTCCTCTAGGTCCCCACATTTACTGCAGGGGGTGTGTGGCGGGGGGGG GTAACAATTTTCAGCTCCTCCTCTAGGTCCCCGCATTTACTGCAGGGGGTGTGTGGCGGGGGGGG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35684208..35684870 26863196 MeRIP-seq:(Medium) rs997594681 Functional Loss SNV dbSNP153 33..33 33 - - - 64280 RMVar_ID_64280 Human_SNP_ID_397317348 m1A Human chr9 - 35689740 35689740 35689740 GAGAACGCCATCGACCGCGCCGAGCAGGCCGAAGCCGACAAGAAGCAAGCTGAGGACCGCTGCAA GAGAACGCCATCGACCGCGCCGAGCAGGCCGAGGCCGACAAGAAGCAAGCTGAGGACCGCTGCAA T C TPM2 Ensembl:ENSG00000198467 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35689726..35689900 32194978 MeRIP-seq:(Medium) rs747252833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92729,Human_RBP_ID_256924,Human_RBP_ID_963142,Human_RBP_ID_9406886,Human_RBP_ID_19024965,Human_RBP_ID_24549592,Human_RBP_ID_27833054 Human_Splice_Rec_1042253,Human_Splice_Rec_1042269,Human_Splice_Rec_1042299,Human_Splice_Rec_1042315,Human_Splice_Rec_1042339,Human_Splice_Rec_1042353 64281 RMVar_ID_64281 Human_SNP_ID_397317459 m1A Human chr9 + 35689953 35689951 35689953 GGACTGGGACGTCCCGGCCACGCGGGCGCCTAAAAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC GGACTGGGACGTCCCGGCCACGCGGGCGCCT__AAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC TAA T RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35689951..35689975 26863196 MeRIP-seq:(Medium) rs1554659813 Functional Loss DEL dbSNP153 32..33 33 - - - 64282 RMVar_ID_64282 Human_SNP_ID_397317462 m1A Human chr9 + 35689953 35689952 35689954 GGACTGGGACGTCCCGGCCACGCGGGCGCCTAAAAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC GGACTGGGACGTCCCGGCCACGCGGGCGCCTTTTAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC AAA TTT RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35689951..35689975 26863196 MeRIP-seq:(Medium) rs376121464 Functional Loss MNV dbSNP153 32..34 33 - - - 64283 RMVar_ID_64283 Human_SNP_ID_397317463 m1A Human chr9 + 35689953 35689953 35689953 GGACTGGGACGTCCCGGCCACGCGGGCGCCTAAAAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC GGACTGGGACGTCCCGGCCACGCGGGCGCCTATAAGGCGGGGAGGGACCGGGCGGGGCCGGCAAC A T RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35689951..35689975 26863196 MeRIP-seq:(Medium) rs3793539 Functional Loss SNV dbSNP153 33..33 33 - - - 64284 RMVar_ID_64284 Human_SNP_ID_397317769 m1A Human chr9 - 35690822 35690822 35690822 GAGCGTCCGCGGGGAGCGGGGGAGAAGAGGGAAGGCGCGCGGAGGGGAGTGGGGCCAGGCGGAGC GAGCGTCCGCGGGGAGCGGGGGAGAAGAGGGAGGGCGCGCGGAGGGGAGTGGGGCCAGGCGGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr9:35690448..35691096;chr9:35690714..35690875 26863196 MeRIP-seq:(Medium) rs1220403289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226529,Human_RBP_ID_21995818,Human_RBP_ID_26796335 64285 RMVar_ID_64285 Human_SNP_ID_397319410 m1A Human chr9 - 35697550 35697550 35697550 TGCCTGCCCCTCCCCAGAGTATTAACGCTCCAAGAGTATTATTAACGCTGCTGTACCTCGATCTG TGCCTGCCCCTCCCCAGAGTATTAACGCTCCAGGAGTATTATTAACGCTGCTGTACCTCGATCTG T C TLN1 Ensembl:ENSG00000137076 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35697526..35697550 26863196 MeRIP-seq:(Medium) rs1397425389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718490,Human_RBP_ID_5329905,Human_RBP_ID_9236328,Human_RBP_ID_17094867,Human_RBP_ID_17666485,Human_RBP_ID_18962768,Human_RBP_ID_23092424 Human_miRNA_ID_1272013,Human_miRNA_ID_2507752,Human_miRNA_ID_2615222,Human_miRNA_ID_2756477 RMVar_hsa_circ_89989,RMVar_hsa_circ_108300,RMVar_hsa_circ_114632,RMVar_hsa_circ_120118,RMVar_hsa_circ_126341,RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_110939,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_105249,RMVar_hsa_circ_99943,RMVar_hsa_circ_94198,RMVar_hsa_circ_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,RMVar_hsa_circ_86173,RMVar_hsa_circ_87647,RMVar_hsa_circ_83735,RMVar_hsa_circ_256648,RMVar_hsa_circ_77776,RMVar_hsa_circ_79607,RMVar_hsa_circ_256650,RMVar_hsa_circ_256652,RMVar_hsa_circ_77354,RMVar_hsa_circ_256651,RMVar_hsa_circ_256649,RMVar_hsa_circ_256646,RMVar_hsa_circ_256647,RMVar_hsa_circ_256645,RMVar_hsa_circ_256640,RMVar_hsa_circ_256642,RMVar_hsa_circ_256643,RMVar_hsa_circ_256641,RMVar_hsa_circ_256638,RMVar_hsa_circ_256639,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631 64286 RMVar_ID_64286 Human_SNP_ID_397319419 m1A Human chr9 - 35697584 35697584 35697584 CCCCAAGTGCCTTCATGCCCTAGGGCCCCCCAAGTGCCTGCCCCTCCCCAGAGTATTAACGCTCC CCCCAAGTGCCTTCATGCCCTAGGGCCCCCCAGGTGCCTGCCCCTCCCCAGAGTATTAACGCTCC T C TLN1 Ensembl:ENSG00000137076 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35697401..35697899 26863196 MeRIP-seq:(Medium) rs564670899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718491,Human_RBP_ID_847177,Human_RBP_ID_5027795,Human_RBP_ID_5135452,Human_RBP_ID_5329905,Human_RBP_ID_8704266,Human_RBP_ID_17094591,Human_RBP_ID_17666699,Human_RBP_ID_18961975 Human_miRNA_ID_1039703,Human_miRNA_ID_2366945,Human_miRNA_ID_2390165,Human_miRNA_ID_2433813,Human_miRNA_ID_2478910,Human_miRNA_ID_2591403,Human_miRNA_ID_2783882,Human_miRNA_ID_3014747 RMVar_hsa_circ_89989,RMVar_hsa_circ_108300,RMVar_hsa_circ_114632,RMVar_hsa_circ_120118,RMVar_hsa_circ_126341,RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_110939,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_105249,RMVar_hsa_circ_99943,RMVar_hsa_circ_94198,RMVar_hsa_circ_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,RMVar_hsa_circ_86173,RMVar_hsa_circ_87647,RMVar_hsa_circ_83735,RMVar_hsa_circ_256648,RMVar_hsa_circ_77776,RMVar_hsa_circ_79607,RMVar_hsa_circ_256650,RMVar_hsa_circ_256652,RMVar_hsa_circ_77354,RMVar_hsa_circ_256651,RMVar_hsa_circ_256649,RMVar_hsa_circ_256646,RMVar_hsa_circ_256647,RMVar_hsa_circ_256645,RMVar_hsa_circ_256640,RMVar_hsa_circ_256642,RMVar_hsa_circ_256643,RMVar_hsa_circ_256641,RMVar_hsa_circ_256638,RMVar_hsa_circ_256639,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631 64287 RMVar_ID_64287 Human_SNP_ID_397322150 m1A Human chr9 + 35707200 35707200 35707200 AGGGCCCGGGCTGTCTGGATGAGTCCCCCGGCACTCTCTAACATTGTCTTGGCAGAGATCACAAT AGGGCCCGGGCTGTCTGGATGAGTCCCCCGGCCCTCTCTAACATTGTCTTGGCAGAGATCACAAT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35707076..35707200 32194978 MeRIP-seq:(Medium) rs1449591031 Functional Loss SNV dbSNP153 33..33 33 - - - 64288 RMVar_ID_64288 Human_SNP_ID_397322199 m1A Human chr9 + 35707366 35707366 35707366 TCACATCGCCTCACCTCAGGGCTGATCTGGGCAGGAATGCTGGAGAACTCAGGGTTGGACGCAAA TCACATCGCCTCACCTCAGGGCTGATCTGGGCGGGAATGCTGGAGAACTCAGGGTTGGACGCAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35707336..35707423 26863196 MeRIP-seq:(Medium) rs1341091351 Functional Loss SNV dbSNP153 33..33 33 - - - 64289 RMVar_ID_64289 Human_SNP_ID_397322228 m1A Human chr9 + 35707473 35707473 35707473 TGCTCGGCACTGGGCACGGTTCTCCTCTGTGAAGGCCCCATCTAGCGCCTAGAAGTGACAGAGAG TGCTCGGCACTGGGCACGGTTCTCCTCTGTGATGGCCCCATCTAGCGCCTAGAAGTGACAGAGAG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35707351..35707475 32194978 MeRIP-seq:(Medium) rs781212644 Functional Loss SNV dbSNP153 33..33 33 - - - 64290 RMVar_ID_64290 Human_SNP_ID_397322505 m1A Human chr9 + 35708452 35708452 35708452 GGCTCCACTAGCCCTTGCTGTCCAGCTTGGCTATTGGGGTCAGAGACACCAACCAGATATGCAGC GGCTCCACTAGCCCTTGCTGTCCAGCTTGGCTGTTGGGGTCAGAGACACCAACCAGATATGCAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35708401..35708475 32194978 MeRIP-seq:(Medium) rs765119784 Functional Loss SNV dbSNP153 33..33 33 - - - 64291 RMVar_ID_64291 Human_SNP_ID_397323644 m1A Human chr9 - 35712077 35712077 35712077 ACCCAGGCTCTGAACCGCTGTGTCAGCTGCCTACCTGGCCAGCGCGATGTGGATAATGCCCTGAG ACCCAGGCTCTGAACCGCTGTGTCAGCTGCCTTCCTGGCCAGCGCGATGTGGATAATGCCCTGAG T A TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35712026..35712125 32194978 MeRIP-seq:(Medium) rs147652402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797518,Human_RBP_ID_5027940,Human_RBP_ID_8928385,Human_RBP_ID_19023814,Human_RBP_ID_23094298 Human_Splice_Rec_1042410,Human_Splice_Rec_1042411 RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_99943,RMVar_hsa_circ_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_83735,RMVar_hsa_circ_256638,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256654,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659,RMVar_hsa_circ_123260,RMVar_hsa_circ_78893,RMVar_hsa_circ_80499,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_95373,RMVar_hsa_circ_89487,RMVar_hsa_circ_256667,RMVar_hsa_circ_256668,RMVar_hsa_circ_256666,RMVar_hsa_circ_90952,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_96699,RMVar_hsa_circ_256675,RMVar_hsa_circ_256679,RMVar_hsa_circ_256681,RMVar_hsa_circ_80565,RMVar_hsa_circ_256680,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_123605,RMVar_hsa_circ_256674,RMVar_hsa_circ_90441,RMVar_hsa_circ_256684,RMVar_hsa_circ_256685,RMVar_hsa_circ_125098,RMVar_hsa_circ_118119,RMVar_hsa_circ_256689,RMVar_hsa_circ_256690,RMVar_hsa_circ_86846,RMVar_hsa_circ_108625,RMVar_hsa_circ_120669,RMVar_hsa_circ_84308,RMVar_hsa_circ_256693,RMVar_hsa_circ_256695,RMVar_hsa_circ_256694,RMVar_hsa_circ_256692,RMVar_hsa_circ_88668,RMVar_hsa_circ_256699,RMVar_hsa_circ_102302,RMVar_hsa_circ_112542,RMVar_hsa_circ_100834,RMVar_hsa_circ_256704,RMVar_hsa_circ_80180,RMVar_hsa_circ_84754,RMVar_hsa_circ_80829,RMVar_hsa_circ_256706,RMVar_hsa_circ_256705,RMVar_hsa_circ_256700,RMVar_hsa_circ_256702,RMVar_hsa_circ_256703,RMVar_hsa_circ_256701,RMVar_hsa_circ_116270,RMVar_hsa_circ_256712,RMVar_hsa_circ_256714,RMVar_hsa_circ_100663,RMVar_hsa_circ_84286,RMVar_hsa_circ_256715,RMVar_hsa_circ_256719,RMVar_hsa_circ_119193,RMVar_hsa_circ_101449,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_77736,RMVar_hsa_circ_124790,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_256722,RMVar_hsa_circ_256725,RMVar_hsa_circ_1552,RMVar_hsa_circ_85007,RMVar_hsa_circ_256726,RMVar_hsa_circ_81316,RMVar_hsa_circ_256728,RMVar_hsa_circ_256729,RMVar_hsa_circ_76800,RMVar_hsa_circ_256730,RMVar_hsa_circ_86014,RMVar_hsa_circ_86312,RMVar_hsa_circ_256731,RMVar_hsa_circ_100421,RMVar_hsa_circ_256732,RMVar_hsa_circ_256733 64292 RMVar_ID_64292 Human_SNP_ID_397323645 m1A Human chr9 - 35712077 35712077 35712077 ACCCAGGCTCTGAACCGCTGTGTCAGCTGCCTACCTGGCCAGCGCGATGTGGATAATGCCCTGAG ACCCAGGCTCTGAACCGCTGTGTCAGCTGCCTCCCTGGCCAGCGCGATGTGGATAATGCCCTGAG T G TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35712026..35712125 32194978 MeRIP-seq:(Medium) rs147652402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797518,Human_RBP_ID_5027940,Human_RBP_ID_8928385,Human_RBP_ID_19023814,Human_RBP_ID_23094298 Human_Splice_Rec_1042410,Human_Splice_Rec_1042411 RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_99943,RMVar_hsa_circ_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_83735,RMVar_hsa_circ_256638,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256654,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659,RMVar_hsa_circ_123260,RMVar_hsa_circ_78893,RMVar_hsa_circ_80499,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_95373,RMVar_hsa_circ_89487,RMVar_hsa_circ_256667,RMVar_hsa_circ_256668,RMVar_hsa_circ_256666,RMVar_hsa_circ_90952,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_96699,RMVar_hsa_circ_256675,RMVar_hsa_circ_256679,RMVar_hsa_circ_256681,RMVar_hsa_circ_80565,RMVar_hsa_circ_256680,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_123605,RMVar_hsa_circ_256674,RMVar_hsa_circ_90441,RMVar_hsa_circ_256684,RMVar_hsa_circ_256685,RMVar_hsa_circ_125098,RMVar_hsa_circ_118119,RMVar_hsa_circ_256689,RMVar_hsa_circ_256690,RMVar_hsa_circ_86846,RMVar_hsa_circ_108625,RMVar_hsa_circ_120669,RMVar_hsa_circ_84308,RMVar_hsa_circ_256693,RMVar_hsa_circ_256695,RMVar_hsa_circ_256694,RMVar_hsa_circ_256692,RMVar_hsa_circ_88668,RMVar_hsa_circ_256699,RMVar_hsa_circ_102302,RMVar_hsa_circ_112542,RMVar_hsa_circ_100834,RMVar_hsa_circ_256704,RMVar_hsa_circ_80180,RMVar_hsa_circ_84754,RMVar_hsa_circ_80829,RMVar_hsa_circ_256706,RMVar_hsa_circ_256705,RMVar_hsa_circ_256700,RMVar_hsa_circ_256702,RMVar_hsa_circ_256703,RMVar_hsa_circ_256701,RMVar_hsa_circ_116270,RMVar_hsa_circ_256712,RMVar_hsa_circ_256714,RMVar_hsa_circ_100663,RMVar_hsa_circ_84286,RMVar_hsa_circ_256715,RMVar_hsa_circ_256719,RMVar_hsa_circ_119193,RMVar_hsa_circ_101449,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_77736,RMVar_hsa_circ_124790,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_256722,RMVar_hsa_circ_256725,RMVar_hsa_circ_1552,RMVar_hsa_circ_85007,RMVar_hsa_circ_256726,RMVar_hsa_circ_81316,RMVar_hsa_circ_256728,RMVar_hsa_circ_256729,RMVar_hsa_circ_76800,RMVar_hsa_circ_256730,RMVar_hsa_circ_86014,RMVar_hsa_circ_86312,RMVar_hsa_circ_256731,RMVar_hsa_circ_100421,RMVar_hsa_circ_256732,RMVar_hsa_circ_256733 64293 RMVar_ID_64293 Human_SNP_ID_397324962 m1A Human chr9 - 35716502 35716502 35716502 CATCCTGGCCCAAGCCACATCTGACCTGGTCAATGCCATCAAGGCTGATGCTGAGGGGGAAAGTG CATCCTGGCCCAAGCCACATCTGACCTGGTCAGTGCCATCAAGGCTGATGCTGAGGGGGAAAGTG T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35716376..35716575 32194978 MeRIP-seq:(Medium) rs145269012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3213044,Human_RBP_ID_18197105 Human_Splice_Rec_1042396 RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_99943,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_83735,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256654,RMVar_hsa_circ_256656,RMVar_hsa_circ_256657,RMVar_hsa_circ_123260,RMVar_hsa_circ_80499,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_256666,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_256674,RMVar_hsa_circ_90441,RMVar_hsa_circ_256685,RMVar_hsa_circ_118119,RMVar_hsa_circ_256690,RMVar_hsa_circ_86846,RMVar_hsa_circ_108625,RMVar_hsa_circ_84308,RMVar_hsa_circ_256693,RMVar_hsa_circ_256694,RMVar_hsa_circ_256692,RMVar_hsa_circ_102302,RMVar_hsa_circ_100834,RMVar_hsa_circ_84754,RMVar_hsa_circ_80829,RMVar_hsa_circ_256700,RMVar_hsa_circ_256702,RMVar_hsa_circ_256703,RMVar_hsa_circ_256701,RMVar_hsa_circ_256714,RMVar_hsa_circ_84286,RMVar_hsa_circ_256719,RMVar_hsa_circ_119193,RMVar_hsa_circ_101449,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_77736,RMVar_hsa_circ_124790,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_256722,RMVar_hsa_circ_256725,RMVar_hsa_circ_1552,RMVar_hsa_circ_85007,RMVar_hsa_circ_256726,RMVar_hsa_circ_81316,RMVar_hsa_circ_256728,RMVar_hsa_circ_256729,RMVar_hsa_circ_76800,RMVar_hsa_circ_256730,RMVar_hsa_circ_86014,RMVar_hsa_circ_86312,RMVar_hsa_circ_256731,RMVar_hsa_circ_106251,RMVar_hsa_circ_100421,RMVar_hsa_circ_256732,RMVar_hsa_circ_256733,RMVar_hsa_circ_52224,RMVar_hsa_circ_28735,RMVar_hsa_circ_49152,RMVar_hsa_circ_59228,RMVar_hsa_circ_256734,RMVar_hsa_circ_85446,RMVar_hsa_circ_82094,RMVar_hsa_circ_256736,RMVar_hsa_circ_256737,RMVar_hsa_circ_110945,RMVar_hsa_circ_256739 64294 RMVar_ID_64294 Human_SNP_ID_397325337 m1A Human chr9 + 35717760 35717760 35717760 TTGAGGACCAGGGCAGCTGCAGCACTTGCCACAGCTTTGGCGAGCTGCATTAGCGCATCCTGTGA TTGAGGACCAGGGCAGCTGCAGCACTTGCCACCGCTTTGGCGAGCTGCATTAGCGCATCCTGTGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35717601..35717800 32194978 MeRIP-seq:(Medium) rs1226450206 Functional Loss SNV dbSNP153 33..33 33 - - - 64295 RMVar_ID_64295 Human_SNP_ID_397326071 m1A Human chr9 + 35720138 35720138 35720138 CCCACCTGGAAATTCTCAGGACCAGAGGCTCCAGAGCGCATGATGGCAGGCAGGGCCACAGAGCC CCCACCTGGAAATTCTCAGGACCAGAGGCTCCGGAGCGCATGATGGCAGGCAGGGCCACAGAGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35720090..35720163 26863196 MeRIP-seq:(Medium) rs1272061567 Functional Loss SNV dbSNP153 33..33 33 - - - 64296 RMVar_ID_64296 Human_SNP_ID_397326169 m1A Human chr9 - 35720461 35720461 35720461 ACTTTGGGCTGGAAGGAGATGAGGAGTCTACTATGCTGGAGGACTCAGTGTCCCCCAAAAAGTAC ACTTTGGGCTGGAAGGAGATGAGGAGTCTACTGTGCTGGAGGACTCAGTGTCCCCCAAAAAGTAC T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35720426..35720500 32194978 MeRIP-seq:(Medium) rs1208571911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965725,Human_RBP_ID_3974489,Human_RBP_ID_5042707,Human_RBP_ID_5482377,Human_RBP_ID_5534694,Human_RBP_ID_8158321,Human_RBP_ID_8928428,Human_RBP_ID_9314754,Human_RBP_ID_9406892,Human_RBP_ID_24549593,Human_RBP_ID_24555404,Human_RBP_ID_26360671,Human_RBP_ID_27136433,Human_RBP_ID_27832356 Human_Splice_Rec_1042380,Human_Splice_Rec_1042381 Human_miRNA_ID_2441252,Human_miRNA_ID_2585063 RMVar_hsa_circ_112957,RMVar_hsa_circ_83735,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631,RMVar_hsa_circ_86505,RMVar_hsa_circ_256654,RMVar_hsa_circ_80499,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_256666,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256676,RMVar_hsa_circ_256674,RMVar_hsa_circ_86846,RMVar_hsa_circ_256692,RMVar_hsa_circ_100834,RMVar_hsa_circ_84754,RMVar_hsa_circ_256700,RMVar_hsa_circ_256701,RMVar_hsa_circ_101449,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_256722,RMVar_hsa_circ_1552,RMVar_hsa_circ_81316,RMVar_hsa_circ_256729,RMVar_hsa_circ_86312,RMVar_hsa_circ_256731,RMVar_hsa_circ_106251,RMVar_hsa_circ_100421,RMVar_hsa_circ_256733,RMVar_hsa_circ_52224,RMVar_hsa_circ_28735,RMVar_hsa_circ_59228,RMVar_hsa_circ_256734,RMVar_hsa_circ_110945,RMVar_hsa_circ_90250,RMVar_hsa_circ_256739,RMVar_hsa_circ_256741,RMVar_hsa_circ_113091,RMVar_hsa_circ_109801,RMVar_hsa_circ_256743,RMVar_hsa_circ_111724,RMVar_hsa_circ_107006,RMVar_hsa_circ_256748,RMVar_hsa_circ_100354,RMVar_hsa_circ_103101,RMVar_hsa_circ_101540,RMVar_hsa_circ_91372,RMVar_hsa_circ_94204,RMVar_hsa_circ_256750,RMVar_hsa_circ_256751,RMVar_hsa_circ_256749,RMVar_hsa_circ_256744,RMVar_hsa_circ_256746,RMVar_hsa_circ_256747,RMVar_hsa_circ_256745,RMVar_hsa_circ_114507,RMVar_hsa_circ_256755,RMVar_hsa_circ_82520,RMVar_hsa_circ_369775,RMVar_hsa_circ_256754,RMVar_hsa_circ_124488,RMVar_hsa_circ_256756,RMVar_hsa_circ_256757 64297 RMVar_ID_64297 Human_SNP_ID_397326651 m1A Human chr9 - 35722213 35722213 35722213 TTCTTCCCCATTTTATGCACAGGCACACAAGAATTGTGGGCAGATGAGTGAGATTGAGGCCAAGG TTCTTCCCCATTTTATGCACAGGCACACAAGAGTTGTGGGCAGATGAGTGAGATTGAGGCCAAGG T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35722101..35722225 32194978 MeRIP-seq:(Medium) rs766292569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961364,Human_RBP_ID_22689930,Human_RBP_ID_24301924 Human_Splice_Rec_1042374,Human_Splice_Rec_1042375 RMVar_hsa_circ_112957,RMVar_hsa_circ_256630,RMVar_hsa_circ_86505,RMVar_hsa_circ_256654,RMVar_hsa_circ_80499,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_256666,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256676,RMVar_hsa_circ_256674,RMVar_hsa_circ_6768,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_1552,RMVar_hsa_circ_106251,RMVar_hsa_circ_100421,RMVar_hsa_circ_256733,RMVar_hsa_circ_52224,RMVar_hsa_circ_28735,RMVar_hsa_circ_59228,RMVar_hsa_circ_256734,RMVar_hsa_circ_90250,RMVar_hsa_circ_256741,RMVar_hsa_circ_109801,RMVar_hsa_circ_111724,RMVar_hsa_circ_256748,RMVar_hsa_circ_103101,RMVar_hsa_circ_101540,RMVar_hsa_circ_91372,RMVar_hsa_circ_94204,RMVar_hsa_circ_256749,RMVar_hsa_circ_256744,RMVar_hsa_circ_256746,RMVar_hsa_circ_256747,RMVar_hsa_circ_256745,RMVar_hsa_circ_114507,RMVar_hsa_circ_256755,RMVar_hsa_circ_369775,RMVar_hsa_circ_124488,RMVar_hsa_circ_256756,RMVar_hsa_circ_256757 64298 RMVar_ID_64298 Human_SNP_ID_397327251 m1A Human chr9 + 35724318 35724318 35724318 TCCTCTACACCCTGCTCCCTCAGTGTCCGACCATGGTCCAGCCAGTTCACTGGGATACAGACAGT TCCTCTACACCCTGCTCCCTCAGTGTCCGACCGTGGTCCAGCCAGTTCACTGGGATACAGACAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35724267..35724367 26863196 MeRIP-seq:(Medium) rs148715883 Functional Loss SNV dbSNP153 33..33 33 - - - 64299 RMVar_ID_64299 Human_SNP_ID_397327257 m1A Human chr9 - 35724336 35724336 35724336 GGGTTTGGCACTGAGGGGACTGTCTGTATCCCAGTGAACTGGCTGGACCATGGTCGGACACTGAG GGGTTTGGCACTGAGGGGACTGTCTGTATCCCCGTGAACTGGCTGGACCATGGTCGGACACTGAG T G TLN1 Ensembl:ENSG00000137076 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35724224..35724365 26863196 MeRIP-seq:(Medium) rs1239426002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5028063,Human_RBP_ID_24549799 RMVar_hsa_circ_86505,RMVar_hsa_circ_256654,RMVar_hsa_circ_88040,RMVar_hsa_circ_256666,RMVar_hsa_circ_84239,RMVar_hsa_circ_256674,RMVar_hsa_circ_6768,RMVar_hsa_circ_102314,RMVar_hsa_circ_256724,RMVar_hsa_circ_1552,RMVar_hsa_circ_100421,RMVar_hsa_circ_256733,RMVar_hsa_circ_90250,RMVar_hsa_circ_256741,RMVar_hsa_circ_109801,RMVar_hsa_circ_111724,RMVar_hsa_circ_103101,RMVar_hsa_circ_256744,RMVar_hsa_circ_256746,RMVar_hsa_circ_256745,RMVar_hsa_circ_30908,RMVar_hsa_circ_256758,RMVar_hsa_circ_111426,RMVar_hsa_circ_9643 64300 RMVar_ID_64300 Human_SNP_ID_397329109 m1A Human chr9 - 35732085 35732085 35732085 GGGCGGCGGGCCGGCGGGCGGGGCGCAGAGCCAGGCAGCGCAGGTAGGCCAGACCGGGCCGGGCG GGGCGGCGGGCCGGCGGGCGGGGCGCAGAGCCGGGCAGCGCAGGTAGGCCAGACCGGGCCGGGCG T C TLN1 Ensembl:ENSG00000137076 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35732076..35732175 26863196 MeRIP-seq:(Medium) rs140986479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268358,Human_RBP_ID_847202,Human_RBP_ID_5035681,Human_RBP_ID_5329464,Human_RBP_ID_9315064,Human_RBP_ID_9339441,Human_RBP_ID_19143380,Human_RBP_ID_22534490,Human_RBP_ID_26360693 Human_Splice_Rec_1042359,Human_Splice_Rec_1042503 Human_miRNA_ID_2083209,Human_miRNA_ID_3068917 RMVar_hsa_circ_100421,RMVar_hsa_circ_256733,RMVar_hsa_circ_90250,RMVar_hsa_circ_256741,RMVar_hsa_circ_109801,RMVar_hsa_circ_256744 64301 RMVar_ID_64301 Human_SNP_ID_397329314 m1A Human chr9 + 35732642 35732642 35732642 CCTGGGAGGCGGGTCCGGAGAGGGCTATGGAAAGCCGCCGGCGGGGAATCCCGGCCGTAGAGGGA CCTGGGAGGCGGGTCCGGAGAGGGCTATGGAACGCCGCCGGCGGGGAATCCCGGCCGTAGAGGGA A C CREB3 Ensembl:ENSG00000107175 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:35732598..35732750;chr9:35732601..35732856 26863196 MeRIP-seq:(Medium) rs1387392080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035682,Human_RBP_ID_5409421,Human_RBP_ID_18427722 64302 RMVar_ID_64302 Human_SNP_ID_397329315 m1A Human chr9 + 35732642 35732642 35732642 CCTGGGAGGCGGGTCCGGAGAGGGCTATGGAAAGCCGCCGGCGGGGAATCCCGGCCGTAGAGGGA CCTGGGAGGCGGGTCCGGAGAGGGCTATGGAAGGCCGCCGGCGGGGAATCCCGGCCGTAGAGGGA A G CREB3 Ensembl:ENSG00000107175 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:35732598..35732750;chr9:35732601..35732856 26863196 MeRIP-seq:(Medium) rs1387392080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035682,Human_RBP_ID_5409421,Human_RBP_ID_18427722 64303 RMVar_ID_64303 Human_SNP_ID_397329324 m1A Human chr9 + 35732676 35732676 35732676 CCGCCGGCGGGGAATCCCGGCCGTAGAGGGACAGTGGATAGGTGCCCGAGGCCTACAGCTGGCCT CCGCCGGCGGGGAATCCCGGCCGTAGAGGGACGGTGGATAGGTGCCCGAGGCCTACAGCTGGCCT A G CREB3 Ensembl:ENSG00000107175 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35732626..35732750 26863196 MeRIP-seq:(Medium) rs116051456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035682,Human_RBP_ID_18427722 64304 RMVar_ID_64304 Human_SNP_ID_397332479 m1A Human chr9 + 35741959 35741958 35741959 CAGGGACCACAGACTAAGTCTTCCCTCTCCTCAAATCAGCTCCTCCCCTTTCAGAGCCTGCAACT CAGGGACCACAGACTAAGTCTTCCCTCTCCTC_AATCAGCTCCTCCCCTTTCAGAGCCTGCAACT CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35741955..35742106 26863196 MeRIP-seq:(Medium) rs1055537346 Functional Loss DEL dbSNP153 33..33 33 - - - 64305 RMVar_ID_64305 Human_SNP_ID_397332480 m1A Human chr9 + 35741964 35741964 35741964 ACCACAGACTAAGTCTTCCCTCTCCTCAAATCAGCTCCTCCCCTTTCAGAGCCTGCAACTGTTAC ACCACAGACTAAGTCTTCCCTCTCCTCAAATCGGCTCCTCCCCTTTCAGAGCCTGCAACTGTTAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:35741960..35742140 26863196 MeRIP-seq:(Medium) rs1421814760 Functional Loss SNV dbSNP153 33..33 33 - - - 64306 RMVar_ID_64306 Human_SNP_ID_397334515 m1A Human chr9 + 35750269 35750269 35750269 CCACAGTGAGGCCCTGGCCTGGGCCAGTGCCCAAATCCACTGCCAGTTCCATGCCAGTGAGAGTC CCACAGTGAGGCCCTGGCCTGGGCCAGTGCCCGAATCCACTGCCAGTTCCATGCCAGTGAGAGTC A G RGP1 Ensembl:ENSG00000107185 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35749386..35750334 32194978 MeRIP-seq:(Medium) rs774950886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964859,Human_RBP_ID_5482105,Human_RBP_ID_5516153,Human_RBP_ID_26240230 Human_Splice_Rec_1042652,Human_Splice_Rec_1042668 Human_miRNA_ID_2457178,Human_miRNA_ID_2462100,Human_miRNA_ID_2506336,Human_miRNA_ID_2634745,Human_miRNA_ID_2637432,Human_miRNA_ID_3042908 RMVar_hsa_circ_256770,RMVar_hsa_circ_346098,RMVar_hsa_circ_374024,RMVar_hsa_circ_7201 64307 RMVar_ID_64307 Human_SNP_ID_397335352 m1A Human chr9 - 35752780 35752780 35752780 TAGGCAGCACCTTGATGGGCAGGTCCCAGCTGAAGGTGTCTACAGGTACTTGCTCAGGTCCTGTC TAGGCAGCACCTTGATGGGCAGGTCCCAGCTGGAGGTGTCTACAGGTACTTGCTCAGGTCCTGTC T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35752730..35752820 26863196 MeRIP-seq:(Medium) rs1563974188 Functional Loss SNV dbSNP153 33..33 33 - - - 64308 RMVar_ID_64308 Human_SNP_ID_397339844 m1A Human chr9 - 35772168 35772168 35772168 CATAACCATGCCGTCACCTGTCACCTTGATGCATATAACTGACAGTAGAAAATGACCTTGTTTCA CATAACCATGCCGTCACCTGTCACCTTGATGCCTATAACTGACAGTAGAAAATGACCTTGTTTCA T G L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:35772160..35772252 26863196 MeRIP-seq:(Medium) rs900522766 Functional Loss SNV dbSNP153 33..33 33 - - - 64309 RMVar_ID_64309 Human_SNP_ID_397350065 m1A Human chr9 + 35813187 35813187 35813187 AGCTTGGGGTTAGGGAGTCAGGATCATGGCAGAGGTCGAAGAATGAAGATCATATTGAGAAGTAG AGCTTGGGGTTAGGGAGTCAGGATCATGGCAGGGGTCGAAGAATGAAGATCATATTGAGAAGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35813185..35813272 26863196 MeRIP-seq:(Medium) rs1221749278 Functional Loss SNV dbSNP153 33..33 33 - - - 64310 RMVar_ID_64310 Human_SNP_ID_397350088 m1A Human chr9 + 35813255 35813255 35813255 TGAGAATTCATAGGTGAGGGACCAAGGGCCAAAAGTCACTCACCAAGTCGGTATCCATCTCCCAG TGAGAATTCATAGGTGAGGGACCAAGGGCCAACAGTCACTCACCAAGTCGGTATCCATCTCCCAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35813251..35813350 32194978 MeRIP-seq:(Medium) rs1380018608 Functional Loss SNV dbSNP153 33..33 33 - - - 64311 RMVar_ID_64311 Human_SNP_ID_397350089 m1A Human chr9 + 35813255 35813255 35813255 TGAGAATTCATAGGTGAGGGACCAAGGGCCAAAAGTCACTCACCAAGTCGGTATCCATCTCCCAG TGAGAATTCATAGGTGAGGGACCAAGGGCCAAGAGTCACTCACCAAGTCGGTATCCATCTCCCAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35813251..35813350 32194978 MeRIP-seq:(Medium) rs1380018608 Functional Loss SNV dbSNP153 33..33 33 - - - 64312 RMVar_ID_64312 Human_SNP_ID_397350542 m1A Human chr9 - 35814698 35814698 35814698 AGAACGAGCTGGTGCTGATTCCCGCCCTGCGCAGGCCGGGGCGCCGAGGTCGGGACAGGGTCAGT AGAACGAGCTGGTGCTGATTCCCGCCCTGCGCGGGCCGGGGCGCCGAGGTCGGGACAGGGTCAGT T C HINT2,AL133410.3 Ensembl:ENSG00000137133,Ensembl:ENSG00000285645 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35814687..35814776 26863196 MeRIP-seq:(Medium) rs989827340 Functional Loss SNV dbSNP153 33..33 33 - - - 64313 RMVar_ID_64313 Human_SNP_ID_397357056 m1A Human chr9 - 35841576 35841576 35841576 ACAGGGGGCAGGCAGATACCCCACGGCCCCCCACACACACCAGCTGTGCTGAAACCCTGTAAGTG ACAGGGGGCAGGCAGATACCCCACGGCCCCCCCCACACACCAGCTGTGCTGAAACCCTGTAAGTG T G L13304-001 RNACentral:URS000044B5AA scRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35835179..35841598 32194978 MeRIP-seq:(Medium) rs1035280287 Functional Loss SNV dbSNP153 33..33 33 - - - 64314 RMVar_ID_64314 Human_SNP_ID_397357244 m1A Human chr9 + 35842439 35842439 35842439 GCCTGCTCCGAGCCCTGGTCCCTGGAGCTGCCATGAACATGCCCCAGTCCCTGGGCAACCAGCCA GCCTGCTCCGAGCCCTGGTCCCTGGAGCTGCCGTGAACATGCCCCAGTCCCTGGGCAACCAGCCA A G TMEM8B Ensembl:ENSG00000137103 Protein coding start codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35841697..35842594 32194978 MeRIP-seq:(Medium) rs752794838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24302117 Human_Splice_Rec_1042998,Human_Splice_Rec_1043016,Human_Splice_Rec_1043034,Human_Splice_Rec_1043060,Human_Splice_Rec_1043086,Human_Splice_Rec_1043108,Human_Splice_Rec_1043118,Human_Splice_Rec_1043144 RMVar_hsa_circ_101633,RMVar_hsa_circ_84727,RMVar_hsa_circ_120488,RMVar_hsa_circ_256777,RMVar_hsa_circ_256778,RMVar_hsa_circ_121648,RMVar_hsa_circ_256779,RMVar_hsa_circ_92137,RMVar_hsa_circ_256780,RMVar_hsa_circ_256781,RMVar_hsa_circ_112339,RMVar_hsa_circ_256782 64315 RMVar_ID_64315 Human_SNP_ID_397372521 m1A Human chr9 + 35906264 35906264 35906264 GAAGGGGAGAAAGGAGTGAGGAGCTGCTGGGCAGAGAGGGACTGTCCGGCTCCCAGATGCTGGGC GAAGGGGAGAAAGGAGTGAGGAGCTGCTGGGCGGAGAGGGACTGTCCGGCTCCCAGATGCTGGGC A G HRCT1 Ensembl:ENSG00000196196 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:35906151..35906983;chr9:35906201..35906600 26863196 MeRIP-seq:(Medium) rs778003739 Functional Loss SNV dbSNP153 33..33 33 - - - 64316 RMVar_ID_64316 Human_SNP_ID_397372536 m1A Human chr9 + 35906286 35906286 35906286 GCTGCTGGGCAGAGAGGGACTGTCCGGCTCCCAGATGCTGGGCCTCCTGGGGAGCACAGCCCTCG GCTGCTGGGCAGAGAGGGACTGTCCGGCTCCCGGATGCTGGGCCTCCTGGGGAGCACAGCCCTCG A G HRCT1 Ensembl:ENSG00000196196 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:35906209..35906559;chr9:35906243..35906373 26863196 MeRIP-seq:(Medium) rs1244033125 Functional Loss SNV dbSNP153 33..33 33 - - - 64317 RMVar_ID_64317 Human_SNP_ID_397386600 m1A Human chr9 - 35962471 35962471 35962471 GGGAGGAACTGAGAATTGCGTGTGGAATCAGGAGACTCAGAAGCGGCCATCGCGCAAGAAGCAGA GGGAGGAACTGAGAATTGCGTGTGGAATCAGGGGACTCAGAAGCGGCCATCGCGCAAGAAGCAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:35962469..35962644 26863196 MeRIP-seq:(Medium) rs1377389182 Functional Loss SNV dbSNP153 33..33 33 - - - 64318 RMVar_ID_64318 Human_SNP_ID_397386607 m1A Human chr9 + 35962519 35962519 35962519 AATTCTCAGTTCCTCCCTGGATCCCTGGCTAGACACTGTGCCAGAGAAAGACCCCCGACATGCCC AATTCTCAGTTCCTCCCTGGATCCCTGGCTAGCCACTGTGCCAGAGAAAGACCCCCGACATGCCC A C OR2S1P Ensembl:ENSG00000228307 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:35962468..35962565 26863196 MeRIP-seq:(Medium) rs888804789 Functional Loss SNV dbSNP153 33..33 33 - - - 64319 RMVar_ID_64319 Human_SNP_ID_397404588 m1A Human chr9 - 36037094 36037094 36037094 TCGAACCGTTGCTCTGGAGGTTACTCACCCGCACTGCCCGGAGCCAGGCCCCCTGCCACCTCCGC TCGAACCGTTGCTCTGGAGGTTACTCACCCGCCCTGCCCGGAGCCAGGCCCCCTGCCACCTCCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:36037051..36037178 26863196 MeRIP-seq:(Medium) rs1486382365 Functional Loss SNV dbSNP153 33..33 33 - - - 64320 RMVar_ID_64320 Human_SNP_ID_397414172 m1A Human chr9 + 36081179 36081179 36081179 GAACAGTGGAGAATGAAGGAAATGGAGATTGGAGGAAGGGCTTACAGGTGAAGGGAACAGTGAGA GAACAGTGGAGAATGAAGGAAATGGAGATTGGGGGAAGGGCTTACAGGTGAAGGGAACAGTGAGA A G RECK Ensembl:ENSG00000122707 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:36081081..36081180 26863196 MeRIP-seq:(Medium) rs1426526293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65264,RMVar_hsa_circ_27545,RMVar_hsa_circ_36531,RMVar_hsa_circ_287212,RMVar_hsa_circ_256794,RMVar_hsa_circ_81754,RMVar_hsa_circ_92034,RMVar_hsa_circ_256797,RMVar_hsa_circ_256798,RMVar_hsa_circ_300235,RMVar_hsa_circ_12302 64321 RMVar_ID_64321 Human_SNP_ID_397427363 m1A Human chr9 + 36136786 36136786 36136786 GAGCGAGGAGCGCGCGGAGCCGGCCATGGGCAAGTCAGGTGAGCCCGCGGGCTCGCCCGCTGCGG GAGCGAGGAGCGCGCGGAGCCGGCCATGGGCATGTCAGGTGAGCCCGCGGGCTCGCCCGCTGCGG A T GLIPR2 Ensembl:ENSG00000122694 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36136763..36136831 26863196 MeRIP-seq:(Medium) rs961238841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1043285,Human_Splice_Rec_1043289,Human_Splice_Rec_1043297,Human_Splice_Rec_1043303 RMVar_hsa_circ_99224,RMVar_hsa_circ_256806 64322 RMVar_ID_64322 Human_SNP_ID_397441382 m1A Human chr9 + 36191177 36191177 36191177 ACCCGGCTGCGGCCTTCTTGGCGCAGCAAGAGAGCGAGATTGCGGGCATCGAGAACGACGAGGCC ACCCGGCTGCGGCCTTCTTGGCGCAGCAAGAGGGCGAGATTGCGGGCATCGAGAACGACGAGGCC A G CLTA Ensembl:ENSG00000122705 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:36191001..36191200 26863196 MeRIP-seq:(Medium) rs757143986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9236366,Human_RBP_ID_16669835,Human_RBP_ID_18140473,Human_RBP_ID_22466384 Human_Splice_Rec_1043315,Human_Splice_Rec_1043319,Human_Splice_Rec_1043329,Human_Splice_Rec_1043337,Human_Splice_Rec_1043345,Human_Splice_Rec_1043359,Human_Splice_Rec_1043369,Human_Splice_Rec_1043381,Human_Splice_Rec_1043389,Human_Splice_Rec_1043399 RMVar_hsa_circ_106208,RMVar_hsa_circ_256808 64323 RMVar_ID_64323 Human_SNP_ID_397442105 m1A Human chr9 - 36193910 36193910 36193910 ACAGCTCCACTTGTGCTGCCTCCTTCATGACCACCTGTTCTTCCTCAATATCCCCCACAGCTGGT ACAGCTCCACTTGTGCTGCCTCCTTCATGACCCCCTGTTCTTCCTCAATATCCCCCACAGCTGGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:36193906..36194005 26863196 MeRIP-seq:(Medium) rs1480235765 Functional Loss SNV dbSNP153 33..33 33 - - - 64324 RMVar_ID_64324 Human_SNP_ID_397444749 m1A Human chr9 + 36204152 36204152 36204152 GCTAGAAGAATGGTATGCAAGACAGGACGAGCAGCTACAGAAAACAAAAGCAAACAACAGGTCAG GCTAGAAGAATGGTATGCAAGACAGGACGAGCGGCTACAGAAAACAAAAGCAAACAACAGGTCAG A G CLTA Ensembl:ENSG00000122705 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36204101..36204220 26863196 MeRIP-seq:(Medium) rs971703406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718701,Human_RBP_ID_966008,Human_RBP_ID_9406917,Human_RBP_ID_16670099,Human_RBP_ID_24302285,Human_RBP_ID_26360702,Human_RBP_ID_27546068,Human_RBP_ID_27833063 Human_Splice_Rec_1043316,Human_Splice_Rec_1043317,Human_Splice_Rec_1043324,Human_Splice_Rec_1043325,Human_Splice_Rec_1043334,Human_Splice_Rec_1043335,Human_Splice_Rec_1043342,Human_Splice_Rec_1043343,Human_Splice_Rec_1043350,Human_Splice_Rec_1043351,Human_Splice_Rec_1043364,Human_Splice_Rec_1043365,Human_Splice_Rec_1043374,Human_Splice_Rec_1043375,Human_Splice_Rec_1043382,Human_Splice_Rec_1043383,Human_Splice_Rec_1043394,Human_Splice_Rec_1043395,Human_Splice_Rec_1043402,Human_Splice_Rec_1043403 Human_miRNA_ID_2359602 RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_279692,RMVar_hsa_circ_256808,RMVar_hsa_circ_256810,RMVar_hsa_circ_256811,RMVar_hsa_circ_13911,RMVar_hsa_circ_256813,RMVar_hsa_circ_121357,RMVar_hsa_circ_295681,RMVar_hsa_circ_256814 64325 RMVar_ID_64325 Human_SNP_ID_397446563 m1A Human chr9 + 36211648 36211648 36211648 GCCTTTGTAAATGACATTGACGAGTCGTCCCCAGGCACTGAGTGGGAACGGGTGGCCCGGCTGTG GCCTTTGTAAATGACATTGACGAGTCGTCCCCCGGCACTGAGTGGGAACGGGTGGCCCGGCTGTG A C CLTA Ensembl:ENSG00000122705 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr9:36211601..36211775;chr9:36211567..36211753 26863196 MeRIP-seq:(Medium) rs201873493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718702,Human_RBP_ID_2064404,Human_RBP_ID_5028557,Human_RBP_ID_7925286,Human_RBP_ID_8704385,Human_RBP_ID_9406919,Human_RBP_ID_16670305,Human_RBP_ID_17716589,Human_RBP_ID_18141116,Human_RBP_ID_18908650,Human_RBP_ID_21906892,Human_RBP_ID_24302302,Human_RBP_ID_26360372,Human_RBP_ID_27785672 Human_Splice_Rec_1043318,Human_Splice_Rec_1043344,Human_Splice_Rec_1043368,Human_Splice_Rec_1043380,Human_Splice_Rec_1043388,Human_Splice_Rec_1043398,Human_Splice_Rec_1043404 Human_miRNA_ID_333748,Human_miRNA_ID_844799 RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_256808,RMVar_hsa_circ_256811,RMVar_hsa_circ_121357,RMVar_hsa_circ_256814,RMVar_hsa_circ_256815,RMVar_hsa_circ_78334,RMVar_hsa_circ_256816,RMVar_hsa_circ_101134 64326 RMVar_ID_64326 Human_SNP_ID_397446564 m1A Human chr9 + 36211648 36211648 36211648 GCCTTTGTAAATGACATTGACGAGTCGTCCCCAGGCACTGAGTGGGAACGGGTGGCCCGGCTGTG GCCTTTGTAAATGACATTGACGAGTCGTCCCCGGGCACTGAGTGGGAACGGGTGGCCCGGCTGTG A G CLTA Ensembl:ENSG00000122705 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr9:36211601..36211775;chr9:36211567..36211753 26863196 MeRIP-seq:(Medium) rs201873493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718702,Human_RBP_ID_2064404,Human_RBP_ID_5028557,Human_RBP_ID_7925286,Human_RBP_ID_8704385,Human_RBP_ID_9406919,Human_RBP_ID_16670305,Human_RBP_ID_17716589,Human_RBP_ID_18141116,Human_RBP_ID_18908650,Human_RBP_ID_21906892,Human_RBP_ID_24302302,Human_RBP_ID_26360372,Human_RBP_ID_27785672 Human_Splice_Rec_1043318,Human_Splice_Rec_1043344,Human_Splice_Rec_1043368,Human_Splice_Rec_1043380,Human_Splice_Rec_1043388,Human_Splice_Rec_1043398,Human_Splice_Rec_1043404 Human_miRNA_ID_333748,Human_miRNA_ID_844799 RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_256808,RMVar_hsa_circ_256811,RMVar_hsa_circ_121357,RMVar_hsa_circ_256814,RMVar_hsa_circ_256815,RMVar_hsa_circ_78334,RMVar_hsa_circ_256816,RMVar_hsa_circ_101134 64327 RMVar_ID_64327 Human_SNP_ID_397446583 m1A Human chr9 + 36211700 36211700 36211700 TGGCCCGGCTGTGTGACTTTAACCCCAAGTCTAGCAAGCAGGCCAAAGATGTCTCCCGCATGCGC TGGCCCGGCTGTGTGACTTTAACCCCAAGTCTGGCAAGCAGGCCAAAGATGTCTCCCGCATGCGC A G CLTA Ensembl:ENSG00000122705 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36211650..36211739 26863196 MeRIP-seq:(Medium) rs775911876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5028563,Human_RBP_ID_8704386,Human_RBP_ID_9406919,Human_RBP_ID_17666706,Human_RBP_ID_18185681,Human_RBP_ID_27136533,Human_RBP_ID_27375276 Human_Splice_Rec_1043318,Human_Splice_Rec_1043344,Human_Splice_Rec_1043368,Human_Splice_Rec_1043380,Human_Splice_Rec_1043388,Human_Splice_Rec_1043398,Human_Splice_Rec_1043404 RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_256808,RMVar_hsa_circ_256811,RMVar_hsa_circ_121357,RMVar_hsa_circ_256814,RMVar_hsa_circ_256815,RMVar_hsa_circ_78334,RMVar_hsa_circ_256816,RMVar_hsa_circ_101134 64328 RMVar_ID_64328 Human_SNP_ID_397446627 m1A Human chr9 - 36211809 36211809 36211809 GACTGTGAAGAGCTTCACTGAGTAGGATTAAGATATTGCAGATGTAGTGTTTCCACAGGGTGGCT GACTGTGAAGAGCTTCACTGAGTAGGATTAAGTTATTGCAGATGTAGTGTTTCCACAGGGTGGCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:36211801..36211825 26863196 MeRIP-seq:(Medium) rs1206101010 Functional Loss SNV dbSNP153 33..33 33 - - - 64329 RMVar_ID_64329 Human_SNP_ID_397446639 m1A Human chr9 - 36211855 36211851 36211856 AGACAAAAAGGTTTGGTCCAAAAGAACTCAACATAATTAATCCAATGACTGTGAAGAGCTTCACT AGACAAAAAGGTTTGGTCCAAAAGAACTCAA_____TTAATCCAATGACTGTGAAGAGCTTCACT ATTATG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36211805..36212000 26863196 MeRIP-seq:(Medium) rs1369914593 Functional Loss DEL dbSNP153 32..36 33 - - - 64330 RMVar_ID_64330 Human_SNP_ID_397447950 m1A Human chr9 - 36216783 36216783 36216783 TGGCGGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCAGGGAGGCGGAGCTG TGGCGGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGGCATGAACCAGGGAGGCGGAGCTG T C GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs999645453 Functional Loss SNV dbSNP153 33..33 33 - - - 64331 RMVar_ID_64331 Human_SNP_ID_397448715 m1A Human chr9 + 36219945 36219945 36219945 AGGAACAATCAGGCCCATCCAGAGACACAACAAGGTGGCCCAGTTCTGCAGCACAGAAGGAGCTT AGGAACAATCAGGCCCATCCAGAGACACAACAGGGTGGCCCAGTTCTGCAGCACAGAAGGAGCTT A G CLTA Ensembl:ENSG00000122705 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:36219895..36222852 32194978 MeRIP-seq:(Medium) rs775369694 Functional Loss SNV dbSNP153 33..33 33 - - - 64332 RMVar_ID_64332 Human_SNP_ID_397459770 m1A Human chr9 + 36265478 36265478 36265478 TGCCATGTATGTGCCATCTCTGCCCTAAGCCAATATCATGAAGAAATCAACAAGAGGTGGAATAA TGCCATGTATGTGCCATCTCTGCCCTAAGCCAGTATCATGAAGAAATCAACAAGAGGTGGAATAA A G CLTA Ensembl:ENSG00000122705 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:36265413..36265516 26863196 MeRIP-seq:(Medium) rs189247743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1043354,Human_Splice_Rec_1043355 64333 RMVar_ID_64333 Human_SNP_ID_397488883 m1A Human chr9 + 36376079 36376079 36376079 TGAGGGAGCTGGTGATGCTGATGTATAATCAAAGACTGAATGAGAGAGGCGCTGTCTCTTAGGAC TGAGGGAGCTGGTGATGCTGATGTATAATCAACGACTGAATGAGAGAGGCGCTGTCTCTTAGGAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36376053..36376156 26863196 MeRIP-seq:(Medium) rs904459306 Functional Loss SNV dbSNP153 33..33 33 - - - 64334 RMVar_ID_64334 Human_SNP_ID_397495753 m1A Human chr9 + 36400646 36400626 36400646 TCCTATTGTGACTGCTCGCCCAGCCCGCGGCCAGCTCGCCAGATCCGCCGTCCGCGGGCCTCCTC TCCTATTGTGACT____________________GCTCGCCAGATCCGCCGTCCGCGGGCCTCCTC TGCTCGCCCAGCCCGCGGCCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:36400631..36400821 26863196 MeRIP-seq:(Medium) rs1451354746 Functional Loss DEL dbSNP153 14..33 33 - - - 64335 RMVar_ID_64335 Human_SNP_ID_397495768 m1A Human chr9 + 36400646 36400646 36400646 TCCTATTGTGACTGCTCGCCCAGCCCGCGGCCAGCTCGCCAGATCCGCCGTCCGCGGGCCTCCTC TCCTATTGTGACTGCTCGCCCAGCCCGCGGCCGGCTCGCCAGATCCGCCGTCCGCGGGCCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:36400631..36400821 26863196 MeRIP-seq:(Medium) rs1351881233 Functional Loss SNV dbSNP153 33..33 33 - - - 64336 RMVar_ID_64336 Human_SNP_ID_397495799 m1A Human chr9 - 36400721 36400721 36400721 CGCGGCCCGTGTGATGGTGCCGGGAGGAAGGAAGCGCAGTGACAGTGCCTAAGTTGGAGCCGGGG CGCGGCCCGTGTGATGGTGCCGGGAGGAAGGAGGCGCAGTGACAGTGCCTAAGTTGGAGCCGGGG T C RNF38 Ensembl:ENSG00000137075 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36400615..36400842 26863196 MeRIP-seq:(Medium) rs1326702196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17175697 RMVar_hsa_circ_122433,RMVar_hsa_circ_256836,RMVar_hsa_circ_106817,RMVar_hsa_circ_256840,RMVar_hsa_circ_121779,RMVar_hsa_circ_256848,RMVar_hsa_circ_256849,RMVar_hsa_circ_123359,RMVar_hsa_circ_275591,RMVar_hsa_circ_256852 64337 RMVar_ID_64337 Human_SNP_ID_397495824 m1A Human chr9 - 36400796 36400796 36400796 GGGGGCGGAGAGGATGGAGCCTCCGAGGCGTTAGGCGACTCTGTCATCTCTGGGCGTGCAGCCGT GGGGGCGGAGAGGATGGAGCCTCCGAGGCGTTTGGCGACTCTGTCATCTCTGGGCGTGCAGCCGT T A RNF38 Ensembl:ENSG00000137075 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:36400593..36400838 26863196 MeRIP-seq:(Medium) rs1380274573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035692,Human_RBP_ID_8224960,Human_RBP_ID_16671285 Human_miRNA_ID_2065136 RMVar_hsa_circ_122433,RMVar_hsa_circ_256836,RMVar_hsa_circ_106817,RMVar_hsa_circ_256840,RMVar_hsa_circ_121779,RMVar_hsa_circ_256848,RMVar_hsa_circ_256849,RMVar_hsa_circ_123359,RMVar_hsa_circ_275591,RMVar_hsa_circ_256852 64338 RMVar_ID_64338 Human_SNP_ID_397518250 m1A Human chr9 - 36486065 36486065 36486065 TGCTGAAGGGCGGGGGACGGTGTCTAGTCTGGAGAAAAAGATTGGGATGTTTCAAAGAAGGTGCC TGCTGAAGGGCGGGGGACGGTGTCTAGTCTGGGGAAAAAGATTGGGATGTTTCAAAGAAGGTGCC T C RNF38 Ensembl:ENSG00000137075 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:36486033..36486250 26863196 MeRIP-seq:(Medium) rs975553736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24302570 64339 RMVar_ID_64339 Human_SNP_ID_397518661 m1A Human chr9 - 36487423 36487423 36487423 GAGCTTGGGCCCCCGCGCCGCCCGCGCCCCCCACCGCCGCCGCCCCGGCCGGAGCCCGCCGCCAC GAGCTTGGGCCCCCGCGCCGCCCGCGCCCCCCCCCGCCGCCGCCCCGGCCGGAGCCCGCCGCCAC T G RNF38 Ensembl:ENSG00000137075 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:36487401..36487563 26863196 MeRIP-seq:(Medium) rs1323616698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5409431 64340 RMVar_ID_64340 Human_SNP_ID_397518722 m1A Human chr9 + 36487592 36487592 36487592 TGGCGGGGCCGCGAGCAGCGGCTCCGGCTGCGACTCGACTCCGGCGCGGCAGGCGCTGGCTGGGC TGGCGGGGCCGCGAGCAGCGGCTCCGGCTGCGGCTCGACTCCGGCGCGGCAGGCGCTGGCTGGGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:36487583..36487747 26863196 MeRIP-seq:(Medium) rs1216183983 Functional Loss SNV dbSNP153 33..33 33 - - - 64341 RMVar_ID_64341 Human_SNP_ID_397562462 m1A Human chr9 + 36655503 36655503 36655503 AGAGAGAGAACGCAAGTGAGCTGGAAGGGTGGACAAGAGCCAGATAGTAGAGAACCTGAAAATGC AGAGAGAGAACGCAAGTGAGCTGGAAGGGTGGGCAAGAGCCAGATAGTAGAGAACCTGAAAATGC A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:36655387..36655573 26863196 MeRIP-seq:(Medium) rs1239218602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7926013,Human_RBP_ID_8704506,Human_RBP_ID_16764865,Human_RBP_ID_24302704 RMVar_hsa_circ_347759,RMVar_hsa_circ_39111,RMVar_hsa_circ_335019,RMVar_hsa_circ_256862,RMVar_hsa_circ_55804,RMVar_hsa_circ_332034,RMVar_hsa_circ_319162,RMVar_hsa_circ_256868,RMVar_hsa_circ_256870,RMVar_hsa_circ_48429,RMVar_hsa_circ_339633,RMVar_hsa_circ_296402,RMVar_hsa_circ_256871 64342 RMVar_ID_64342 Human_SNP_ID_397566222 m1A Human chr9 + 36671126 36671126 36671126 GGATAAGGTTATCACTGTGCTCACCAGGAGCAAAAGGAAGGGTTCTGCCAGAGACGGGCCCAGAA GGATAAGGTTATCACTGTGCTCACCAGGAGCAGAAGGAAGGGTTCTGCCAGAGACGGGCCCAGAA A G MELK Ensembl:ENSG00000165304 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:36671001..36671175 32194978 MeRIP-seq:(Medium) rs147882939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974498,Human_RBP_ID_5634128,Human_RBP_ID_17322233,Human_RBP_ID_24302771 Human_Splice_Rec_1043729,Human_Splice_Rec_1043761,Human_Splice_Rec_1043793,Human_Splice_Rec_1043823,Human_Splice_Rec_1043857,Human_Splice_Rec_1043885,Human_Splice_Rec_1043919,Human_Splice_Rec_1043975,Human_Splice_Rec_1044037 RMVar_hsa_circ_5879,RMVar_hsa_circ_347759,RMVar_hsa_circ_335019,RMVar_hsa_circ_256862,RMVar_hsa_circ_332034,RMVar_hsa_circ_319162,RMVar_hsa_circ_256868,RMVar_hsa_circ_48429,RMVar_hsa_circ_339633,RMVar_hsa_circ_256871,RMVar_hsa_circ_276309,RMVar_hsa_circ_323687,RMVar_hsa_circ_342832,RMVar_hsa_circ_256872,RMVar_hsa_circ_296480 64343 RMVar_ID_64343 Human_SNP_ID_397566223 m1A Human chr9 + 36671126 36671126 36671126 GGATAAGGTTATCACTGTGCTCACCAGGAGCAAAAGGAAGGGTTCTGCCAGAGACGGGCCCAGAA GGATAAGGTTATCACTGTGCTCACCAGGAGCATAAGGAAGGGTTCTGCCAGAGACGGGCCCAGAA A T MELK Ensembl:ENSG00000165304 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:36671001..36671175 32194978 MeRIP-seq:(Medium) rs147882939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974498,Human_RBP_ID_5634128,Human_RBP_ID_17322233,Human_RBP_ID_24302771 Human_Splice_Rec_1043729,Human_Splice_Rec_1043761,Human_Splice_Rec_1043793,Human_Splice_Rec_1043823,Human_Splice_Rec_1043857,Human_Splice_Rec_1043885,Human_Splice_Rec_1043919,Human_Splice_Rec_1043975,Human_Splice_Rec_1044037 RMVar_hsa_circ_5879,RMVar_hsa_circ_347759,RMVar_hsa_circ_335019,RMVar_hsa_circ_256862,RMVar_hsa_circ_332034,RMVar_hsa_circ_319162,RMVar_hsa_circ_256868,RMVar_hsa_circ_48429,RMVar_hsa_circ_339633,RMVar_hsa_circ_256871,RMVar_hsa_circ_276309,RMVar_hsa_circ_323687,RMVar_hsa_circ_342832,RMVar_hsa_circ_256872,RMVar_hsa_circ_296480 64344 RMVar_ID_64344 Human_SNP_ID_397668828 m1A Human chr9 - 37080024 37080024 37080024 TCGGGGTCCGTCACATACATACTCACTGCCGTAGCTGCAAACAGAAAGCACCAAACAGGGACCAA TCGGGGTCCGTCACATACATACTCACTGCCGTTGCTGCAAACAGAAAGCACCAAACAGGGACCAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:37079975..37080081 26863196 MeRIP-seq:(Medium) rs1456671636 Functional Loss SNV dbSNP153 33..33 33 - - - 64345 RMVar_ID_64345 Human_SNP_ID_397668829 m1A Human chr9 + 37080025 37080025 37080025 TGGTCCCTGTTTGGTGCTTTCTGTTTGCAGCTACGGCAGTGAGTATGTATGTGACGGACCCCGAG TGGTCCCTGTTTGGTGCTTTCTGTTTGCAGCTGCGGCAGTGAGTATGTATGTGACGGACCCCGAG A G EBLN3P Ensembl:ENSG00000281649 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:37079976..37080150 26863196 MeRIP-seq:(Medium) rs1386099090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1118665,Human_RBP_ID_1708125,Human_RBP_ID_5037646,Human_RBP_ID_16673782,Human_RBP_ID_18467249,Human_RBP_ID_22119621,Human_RBP_ID_24302846 Human_Splice_Rec_1044309,Human_Splice_Rec_1044311,Human_Splice_Rec_1044313,Human_Splice_Rec_1044317,Human_Splice_Rec_1044321,Human_Splice_Rec_1044329,Human_Splice_Rec_1044333,Human_Splice_Rec_1044337,Human_Splice_Rec_1044341,Human_Splice_Rec_1044343,Human_Splice_Rec_1044349,Human_Splice_Rec_1044353,Human_Splice_Rec_1044355,Human_Splice_Rec_1044357 64346 RMVar_ID_64346 Human_SNP_ID_397668835 m1A Human chr9 + 37080046 37080046 37080046 TGTTTGCAGCTACGGCAGTGAGTATGTATGTGACGGACCCCGAGTCACCCGCGGCCTGGGACCCC TGTTTGCAGCTACGGCAGTGAGTATGTATGTGGCGGACCCCGAGTCACCCGCGGCCTGGGACCCC A G EBLN3P Ensembl:ENSG00000281649 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:37079976..37080175 26863196 MeRIP-seq:(Medium) rs1179580200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256957,Human_RBP_ID_964605,Human_RBP_ID_1119196,Human_RBP_ID_1708125,Human_RBP_ID_5028768,Human_RBP_ID_5659180,Human_RBP_ID_8731085,Human_RBP_ID_9338910,Human_RBP_ID_16673782,Human_RBP_ID_18467249,Human_RBP_ID_22119621,Human_RBP_ID_24302847 64347 RMVar_ID_64347 Human_SNP_ID_397668841 m1A Human chr9 - 37080058 37080058 37080058 GGAGGGTAGGCAGGGGTCCCAGGCCGCGGGTGACTCGGGGTCCGTCACATACATACTCACTGCCG GGAGGGTAGGCAGGGGTCCCAGGCCGCGGGTGGCTCGGGGTCCGTCACATACATACTCACTGCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:37080026..37080248 26863196 MeRIP-seq:(Medium) rs1267544315 Functional Loss SNV dbSNP153 33..33 33 - - - 64348 RMVar_ID_64348 Human_SNP_ID_397678336 m1A Human chr9 - 37120625 37120622 37120626 GCGGGCGGCGGGGGTCCGTCACACACATACTCACTGCCGCAGCTGCGAACAGGAAGCACCAACCG GCGGGCGGCGGGGGTCCGTCACACACATACT____GCCGCAGCTGCGAACAGGAAGCACCAACCG CAGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:37120607..37120764;chr9:37120607..37120723 26863196 MeRIP-seq:(Medium) rs1440173972 Functional Loss DEL dbSNP153 32..35 33 - - - 64349 RMVar_ID_64349 Human_SNP_ID_397702373 m1A Human chr9 + 37220007 37220004 37220008 GAAGTGAAAATGAGGTGTGGTATTAATAAGGAAAGAAAGGGTTGATTACCAGATGAAAGAGTTTG GAAGTGAAAATGAGGTGTGGTATTAATAAG____GAAAGGGTTGATTACCAGATGAAAGAGTTTG GGAAA G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37219956..37220078 26863196 MeRIP-seq:(Medium) rs1186735428 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3214355,Human_RBP_ID_23300676 RMVar_hsa_circ_87045,RMVar_hsa_circ_122994,RMVar_hsa_circ_256878,RMVar_hsa_circ_88116,RMVar_hsa_circ_256879,RMVar_hsa_circ_110737,RMVar_hsa_circ_256881,RMVar_hsa_circ_256882,RMVar_hsa_circ_256886,RMVar_hsa_circ_270512,RMVar_hsa_circ_284046,RMVar_hsa_circ_306931,RMVar_hsa_circ_334171,RMVar_hsa_circ_286077,RMVar_hsa_circ_92764,RMVar_hsa_circ_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 64350 RMVar_ID_64350 Human_SNP_ID_397702375 m1A Human chr9 + 37220007 37220007 37220007 GAAGTGAAAATGAGGTGTGGTATTAATAAGGAAAGAAAGGGTTGATTACCAGATGAAAGAGTTTG GAAGTGAAAATGAGGTGTGGTATTAATAAGGAGAGAAAGGGTTGATTACCAGATGAAAGAGTTTG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37219956..37220078 26863196 MeRIP-seq:(Medium) rs1450242436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3214355,Human_RBP_ID_23300676 RMVar_hsa_circ_87045,RMVar_hsa_circ_122994,RMVar_hsa_circ_256878,RMVar_hsa_circ_88116,RMVar_hsa_circ_256879,RMVar_hsa_circ_110737,RMVar_hsa_circ_256881,RMVar_hsa_circ_256882,RMVar_hsa_circ_256886,RMVar_hsa_circ_270512,RMVar_hsa_circ_284046,RMVar_hsa_circ_306931,RMVar_hsa_circ_334171,RMVar_hsa_circ_286077,RMVar_hsa_circ_92764,RMVar_hsa_circ_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 64351 RMVar_ID_64351 Human_SNP_ID_397750796 m1A Human chr9 - 37422752 37422752 37422752 TGACGAACACCTTCATGAGTCGCACCGGTCTCATCCGCAGTGCAGCCGCCGACCCGGACCTGGCA TGACGAACACCTTCATGAGTCGCACCGGTCTCCTCCGCAGTGCAGCCGCCGACCCGGACCTGGCA T G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr9:37422701..37422901;chr9:37422676..37422935;chr9:37422701..37422920;chr9:37422676..37422920;chr9:37422701..37422850 26863196 MeRIP-seq:(Medium) rs1554746097 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_249 64352 RMVar_ID_64352 Human_SNP_ID_397751302 m1A Human chr9 + 37424787 37424787 37424787 AGGGCCATCAGAGGCCAGGATTCCCAGCTGGGAGGGGCGGGGACAGGTGTGCGGCTCCTGCTTCT AGGGCCATCAGAGGCCAGGATTCCCAGCTGGGCGGGGCGGGGACAGGTGTGCGGCTCCTGCTTCT A C GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:37424785..37424950 26863196 MeRIP-seq:(Medium) rs1014432583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905 64353 RMVar_ID_64353 Human_SNP_ID_397751309 m1A Human chr9 + 37424797 37424797 37424797 GAGGCCAGGATTCCCAGCTGGGAGGGGCGGGGACAGGTGTGCGGCTCCTGCTTCTCCTGAGGGCC GAGGCCAGGATTCCCAGCTGGGAGGGGCGGGGGCAGGTGTGCGGCTCCTGCTTCTCCTGAGGGCC A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:37424790..37425011 26863196 MeRIP-seq:(Medium) rs1340648485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905 64354 RMVar_ID_64354 Human_SNP_ID_397751648 m1A Human chr9 - 37425996 37425996 37425996 TCTAGGCCCCCTCCAGATCCCAAGCTGCAGTTACCGCTTCTTGATTTCATCCAAAGCCAAGTGGT TCTAGGCCCCCTCCAGATCCCAAGCTGCAGTTGCCGCTTCTTGATTTCATCCAAAGCCAAGTGGT T C RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37425885..37426034 26863196 MeRIP-seq:(Medium) rs1564297234 Functional Loss SNV dbSNP153 33..33 33 - - - 64355 RMVar_ID_64355 Human_SNP_ID_397751768 m1A Human chr9 + 37426542 37426542 37426542 ATGTTACCACCAGATGTCTGATTCGTAGTGGGATCCGAGTTGGCTACACCCCAGATGTCCTGACA ATGTTACCACCAGATGTCTGATTCGTAGTGGGTTCCGAGTTGGCTACACCCCAGATGTCCTGACA A T GRHPR Ensembl:ENSG00000137106 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:37426526..37427770 32194978 MeRIP-seq:(Medium) rs374332294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961378,Human_RBP_ID_9351892,Human_RBP_ID_16678690 Human_Splice_Rec_1044484,Human_Splice_Rec_1044492,Human_Splice_Rec_1044508,Human_Splice_Rec_1044528,Human_Splice_Rec_1044550 RMVar_hsa_circ_84147,RMVar_hsa_circ_122450,RMVar_hsa_circ_127983,RMVar_hsa_circ_298731,RMVar_hsa_circ_256905,RMVar_hsa_circ_270566,RMVar_hsa_circ_112553,RMVar_hsa_circ_256906,RMVar_hsa_circ_256908,RMVar_hsa_circ_256909,RMVar_hsa_circ_256910,RMVar_hsa_circ_256907,RMVar_hsa_circ_84942,RMVar_hsa_circ_87063,RMVar_hsa_circ_276783,RMVar_hsa_circ_46332,RMVar_hsa_circ_256912,RMVar_hsa_circ_256913,RMVar_hsa_circ_256911 64356 RMVar_ID_64356 Human_SNP_ID_397752349 m1A Human chr9 - 37428574 37428574 37428574 CCGGGGCGGGCAAGCGGGCCGGTGGGAGCCTCACCTATGCGCCCCAGCCCGATGATGCCGACAGT CCGGGGCGGGCAAGCGGGCCGGTGGGAGCCTCTCCTATGCGCCCCAGCCCGATGATGCCGACAGT T A RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:37428556..37428634;chr9:37428564..37428648 26863196 MeRIP-seq:(Medium) rs180177313 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_250 64357 RMVar_ID_64357 Human_SNP_ID_397752740 m1A Human chr9 + 37429800 37429800 37429800 TCCAGAGATTTCTGTACACAGGGCGCCAGCCCAGGCCTGAGGAAGCAGCAGAATTCCAGGCAGAG TCCAGAGATTTCTGTACACAGGGCGCCAGCCCGGGCCTGAGGAAGCAGCAGAATTCCAGGCAGAG A G GRHPR Ensembl:ENSG00000137106 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:37429751..37429850 32194978 MeRIP-seq:(Medium) rs1208607338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1044496,Human_Splice_Rec_1044497,Human_Splice_Rec_1044512,Human_Splice_Rec_1044513,Human_Splice_Rec_1044532,Human_Splice_Rec_1044533,Human_Splice_Rec_1044538,Human_Splice_Rec_1044539,Human_Splice_Rec_1044554,Human_Splice_Rec_1044555,Human_Splice_Rec_1044563,Human_Splice_Rec_1044569,Human_Splice_Rec_1044573 Human_miRNA_ID_2553714,Human_miRNA_ID_2998548 RMVar_hsa_circ_13733,RMVar_hsa_circ_122450,RMVar_hsa_circ_127983,RMVar_hsa_circ_298731,RMVar_hsa_circ_256905,RMVar_hsa_circ_256906,RMVar_hsa_circ_256907,RMVar_hsa_circ_87063,RMVar_hsa_circ_256913,RMVar_hsa_circ_256914,RMVar_hsa_circ_329994,RMVar_hsa_circ_106274,RMVar_hsa_circ_256915 64358 RMVar_ID_64358 Human_SNP_ID_397753406 m1A Human chr9 - 37432061 37432061 37432061 CTGGGCTCGTCACATCCAGTCCAGCAGCTGCAATCTTACCACTGGCCAAGGCCTGGTACAGGTCG CTGGGCTCGTCACATCCAGTCCAGCAGCTGCAGTCTTACCACTGGCCAAGGCCTGGTACAGGTCG T C RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37431955..37432125 32194978 MeRIP-seq:(Medium) rs1205587022 Functional Loss SNV dbSNP153 33..33 33 - - - 64359 RMVar_ID_64359 Human_SNP_ID_397753407 m1A Human chr9 - 37432061 37432061 37432061 CTGGGCTCGTCACATCCAGTCCAGCAGCTGCAATCTTACCACTGGCCAAGGCCTGGTACAGGTCG CTGGGCTCGTCACATCCAGTCCAGCAGCTGCACTCTTACCACTGGCCAAGGCCTGGTACAGGTCG T G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37431955..37432125 32194978 MeRIP-seq:(Medium) rs1205587022 Functional Loss SNV dbSNP153 33..33 33 - - - 64360 RMVar_ID_64360 Human_SNP_ID_397754662 m1A Human chr9 + 37436747 37436745 37436747 TGTTGGCAGCTAACAACTTGCTGGCTGGCCTGAGAGGGGAGCCGATGCCTAGTGAACTCAAGCTG TGTTGGCAGCTAACAACTTGCTGGCTGGCCT__GAGGGGAGCCGATGCCTAGTGAACTCAAGCTG TGA T GRHPR Ensembl:ENSG00000137106 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:37436697..37436864 26863196 MeRIP-seq:(Medium) rs1554749672 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_183163,Human_RBP_ID_9236588,Human_RBP_ID_18196897,Human_RBP_ID_26833968 Human_Splice_Rec_1044502,Human_Splice_Rec_1044518,Human_Splice_Rec_1044544,Human_Splice_Rec_1044562,Human_Splice_Rec_1044568 Clinvar_Rec_251 RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 64361 RMVar_ID_64361 Human_SNP_ID_397755836 m1A Human chr9 - 37440991 37440984 37440991 GTTTGGGCCTCCACTCCTCCTTCTCCAGGGTAATGATAGGTTCCCCAAGGGGAGGAGCCAGTAAC GTTTGGGCCTCCACTCCTCCTTCTCCAGGGTA_______GTTCCCCAAGGGGAGGAGCCAGTAAC CCTATCAT C ZBTB5 Ensembl:ENSG00000168795 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37440899..37440999 32194978 MeRIP-seq:(Medium) rs758098028 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_17716612,Human_RBP_ID_18136178,Human_RBP_ID_22340416 64362 RMVar_ID_64362 Human_SNP_ID_397761605 m1A Human chr9 - 37464588 37464588 37464588 TGCCGTCCCATCTTCTCCTGTTTGGAGGACAGATTTGTATGTAAATAATAAAAGGCAGTGAATTA TGCCGTCCCATCTTCTCCTGTTTGGAGGACAGTTTTGTATGTAAATAATAAAAGGCAGTGAATTA T A ZBTB5 Ensembl:ENSG00000168795 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37464581..37464659 32194978 MeRIP-seq:(Medium) rs1031367232 Functional Loss SNV dbSNP153 33..33 33 - - - 64363 RMVar_ID_64363 Human_SNP_ID_397761776 m1A Human chr9 - 37465138 37465119 37465139 ACGTGGGGAAGGTTGAGCACCAGGGGCGCGCCAAGGCGTCGGGGAGCGCGCAGACGTGTACTGGT ACGTGGGGAAGGTTGAGCACCAGGGGCGCGC____________________AGACGTGTACTGGT TGCGCGCTCCCCGACGCCTTG T ZBTB5 Ensembl:ENSG00000168795 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:37465127..37465298 26863196 MeRIP-seq:(Medium) rs1344648969 Functional Loss DEL dbSNP153 32..51 33 - - - Human_RBP_ID_3906270 64364 RMVar_ID_64364 Human_SNP_ID_397761855 m1A Human chr9 - 37465308 37465308 37465308 GGGGAGGAAGTCCCGTAACGGAGACGCTGGTCAGGACGTTCCCACCTCCTCTGACACTGCCGAGT GGGGAGGAAGTCCCGTAACGGAGACGCTGGTCTGGACGTTCCCACCTCCTCTGACACTGCCGAGT T A ZBTB5 Ensembl:ENSG00000168795 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37465049..37465327 26863196 MeRIP-seq:(Medium) rs1299288734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798427,Human_RBP_ID_1705372,Human_RBP_ID_3906271,Human_RBP_ID_5154399,Human_RBP_ID_5535336,Human_RBP_ID_7927717,Human_RBP_ID_8238923,Human_RBP_ID_8930551,Human_RBP_ID_9315066,Human_RBP_ID_9339447,Human_RBP_ID_9351716,Human_RBP_ID_9441919,Human_RBP_ID_18427768,Human_RBP_ID_18467250,Human_RBP_ID_22119258,Human_RBP_ID_22466839,Human_RBP_ID_26772541,Human_RBP_ID_27136749 Human_Splice_Rec_1044581 64365 RMVar_ID_64365 Human_SNP_ID_397761856 m1A Human chr9 - 37465308 37465308 37465308 GGGGAGGAAGTCCCGTAACGGAGACGCTGGTCAGGACGTTCCCACCTCCTCTGACACTGCCGAGT GGGGAGGAAGTCCCGTAACGGAGACGCTGGTCGGGACGTTCCCACCTCCTCTGACACTGCCGAGT T C ZBTB5 Ensembl:ENSG00000168795 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37465049..37465327 26863196 MeRIP-seq:(Medium) rs1299288734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798427,Human_RBP_ID_1705372,Human_RBP_ID_3906271,Human_RBP_ID_5154399,Human_RBP_ID_5535336,Human_RBP_ID_7927717,Human_RBP_ID_8238923,Human_RBP_ID_8930551,Human_RBP_ID_9315066,Human_RBP_ID_9339447,Human_RBP_ID_9351716,Human_RBP_ID_9441919,Human_RBP_ID_18427768,Human_RBP_ID_18467250,Human_RBP_ID_22119258,Human_RBP_ID_22466839,Human_RBP_ID_26772541,Human_RBP_ID_27136749 Human_Splice_Rec_1044581 64366 RMVar_ID_64366 Human_SNP_ID_397767307 m1A Human chr9 + 37486037 37486037 37486037 TGCTGCTGTCTTAACTCCTGTGCTTGGCGGACAGACAGGCGAGATGGCGGCGGAGGTGTTGCCGA TGCTGCTGTCTTAACTCCTGTGCTTGGCGGACGGACAGGCGAGATGGCGGCGGAGGTGTTGCCGA A G POLR1E Ensembl:ENSG00000137054 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:37485986..37486114 26863196 MeRIP-seq:(Medium) rs1325632986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_719057,Human_RBP_ID_3975422,Human_RBP_ID_5036171,Human_RBP_ID_8930061,Human_RBP_ID_9338913,Human_RBP_ID_9408054,Human_RBP_ID_18427295 Human_Splice_Rec_1044583,Human_Splice_Rec_1044605 64367 RMVar_ID_64367 Human_SNP_ID_397767330 m1A Human chr9 + 37486082 37486082 37486082 GGCGGCGGAGGTGTTGCCGAGTGCGAGGTGGCAGTATTGTGGGGCGCCCGACGGGAGCCAGAGAG GGCGGCGGAGGTGTTGCCGAGTGCGAGGTGGCGGTATTGTGGGGCGCCCGACGGGAGCCAGAGAG A G POLR1E Ensembl:ENSG00000137054 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:37486032..37486161 32194978 MeRIP-seq:(Medium) rs778327268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798735,Human_RBP_ID_5036171,Human_RBP_ID_8930061,Human_RBP_ID_8944620,Human_RBP_ID_9315563,Human_RBP_ID_9338913,Human_RBP_ID_9408054,Human_RBP_ID_19025016,Human_RBP_ID_23216460 Human_Splice_Rec_1044583,Human_Splice_Rec_1044605 64368 RMVar_ID_64368 Human_SNP_ID_397771729 m1A Human chr9 + 37503493 37503493 37503493 CCAGCTACTCGGGAGGCTGAGGCAGGACGATTACTTGAGCTTGGGAAATCAAGGTTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAGGACGATTGCTTGAGCTTGGGAAATCAAGGTTGCAGTGAGC A G POLR1E Ensembl:ENSG00000137054 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1128859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16679652 RMVar_hsa_circ_96685,RMVar_hsa_circ_85482,RMVar_hsa_circ_256918,RMVar_hsa_circ_256919,RMVar_hsa_circ_107420,RMVar_hsa_circ_89019,RMVar_hsa_circ_256920,RMVar_hsa_circ_119315,RMVar_hsa_circ_256924,RMVar_hsa_circ_256925 64369 RMVar_ID_64369 Human_SNP_ID_397772880 m1A Human chr9 + 37508782 37508782 37508782 AACCCAGGAGGGCAGCAGACCCCAGGGGGATGAGGGTGCTGCCTGCAAATCTCTGAAGAGTTGTC AACCCAGGAGGGCAGCAGACCCCAGGGGGATGCGGGTGCTGCCTGCAAATCTCTGAAGAGTTGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37508734..37509133 26863196 MeRIP-seq:(Medium) rs1021580065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18908918 64370 RMVar_ID_64370 Human_SNP_ID_397772881 m1A Human chr9 + 37508782 37508782 37508782 AACCCAGGAGGGCAGCAGACCCCAGGGGGATGAGGGTGCTGCCTGCAAATCTCTGAAGAGTTGTC AACCCAGGAGGGCAGCAGACCCCAGGGGGATGGGGGTGCTGCCTGCAAATCTCTGAAGAGTTGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37508734..37509133 26863196 MeRIP-seq:(Medium) rs1021580065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18908918 64371 RMVar_ID_64371 Human_SNP_ID_397789189 m1A Human chr9 + 37576270 37576270 37576270 TCCGGGCCGCGGCCGCCGGTGCCCTGGAAGCCACCCGCCGCCCCCGCTGGAGCCGCAGCAGCCGG TCCGGGCCGCGGCCGCCGGTGCCCTGGAAGCCCCCCGCCGCCCCCGCTGGAGCCGCAGCAGCCGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:37576170..37576340 26863410 MeRIP-seq:(Medium) rs933937039 Functional Loss SNV dbSNP153 33..33 33 - - - 64372 RMVar_ID_64372 Human_SNP_ID_397792930 m1A Human chr9 + 37592531 37592531 37592531 CCAGCTTCGGCGCGAGGCCCTCAATCCGGAACATCGCGGCTCTGACTTAGCAGCTTCCAGCCGCC CCAGCTTCGGCGCGAGGCCCTCAATCCGGAACGTCGCGGCTCTGACTTAGCAGCTTCCAGCCGCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:37592451..37592600 26863410 MeRIP-seq:(Medium) rs1274270822 Functional Loss SNV dbSNP153 33..33 33 - - - 64373 RMVar_ID_64373 Human_SNP_ID_397792950 m1A Human chr9 + 37592550 37592550 37592550 CTCAATCCGGAACATCGCGGCTCTGACTTAGCAGCTTCCAGCCGCCGCGCTCTGCTCTCCACGGT CTCAATCCGGAACATCGCGGCTCTGACTTAGCGGCTTCCAGCCGCCGCGCTCTGCTCTCCACGGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:37592501..37592600 26863196 MeRIP-seq:(Medium) rs374065739 Functional Loss SNV dbSNP153 33..33 33 - - - 64374 RMVar_ID_64374 Human_SNP_ID_397792953 m1A Human chr9 - 37592553 37592553 37592553 GCCACCGTGGAGAGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCAGAGCCGCGATGTTCCGGATT GCCACCGTGGAGAGCAGAGCGCGGCGGCTGGAGGCTGCTAAGTCAGAGCCGCGATGTTCCGGATT T C AL138752.2,TOMM5 Ensembl:ENSG00000255872,Ensembl:ENSG00000175768 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:37592361..37592625;chr9:37588851..37592625 26863196 MeRIP-seq:(Medium) rs997501605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_719110,Human_RBP_ID_1705406,Human_RBP_ID_5029157,Human_RBP_ID_22466840,Human_RBP_ID_26360374 64375 RMVar_ID_64375 Human_SNP_ID_397792954 m1A Human chr9 - 37592554 37592554 37592554 GGCCACCGTGGAGAGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCAGAGCCGCGATGTTCCGGAT GGCCACCGTGGAGAGCAGAGCGCGGCGGCTGGGAGCTGCTAAGTCAGAGCCGCGATGTTCCGGAT T C AL138752.2,TOMM5 Ensembl:ENSG00000255872,Ensembl:ENSG00000175768 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:37592474..37592563 26863410 MeRIP-seq:(Medium) rs1327049348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_719110,Human_RBP_ID_5029157,Human_RBP_ID_22466840,Human_RBP_ID_26360374 64376 RMVar_ID_64376 Human_SNP_ID_397792966 m1A Human chr9 - 37592573 37592573 37592573 CGAGTTCCGGGCGCGAGGCGGCCACCGTGGAGAGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCA CGAGTTCCGGGCGCGAGGCGGCCACCGTGGAGGGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCA T C AL138752.2,TOMM5 Ensembl:ENSG00000255872,Ensembl:ENSG00000175768 Protein coding,Protein coding intron,5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1289094002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798435,Human_RBP_ID_5035695,Human_RBP_ID_22466840,Human_RBP_ID_26360374 64377 RMVar_ID_64377 Human_SNP_ID_397831780 m1A Human chr9 + 37753848 37753848 37753848 GCGCGCCGCTGCCGCTGCGTGGGGGTGAGGGGATCAGGTACGCTGTCCGCTGGTTAAGGGGGCTG GCGCGCCGCTGCCGCTGCGTGGGGGTGAGGGGTTCAGGTACGCTGTCCGCTGGTTAAGGGGGCTG A T TRMT10B Ensembl:ENSG00000165275 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:37753821..37753926 26863196 MeRIP-seq:(Medium) rs1357369632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15320,Human_RBP_ID_24303518 Human_Splice_Rec_1044843,Human_Splice_Rec_1044855,Human_Splice_Rec_1044869,Human_Splice_Rec_1044885,Human_Splice_Rec_1044891,Human_Splice_Rec_1044897,Human_Splice_Rec_1044909,Human_Splice_Rec_1044925 64378 RMVar_ID_64378 Human_SNP_ID_397831781 m1A Human chr9 - 37753849 37753849 37753849 CCAGCCCCCTTAACCAGCGGACAGCGTACCTGATCCCCTCACCCCCACGCAGCGGCAGCGGCGCG CCAGCCCCCTTAACCAGCGGACAGCGTACCTGGTCCCCTCACCCCCACGCAGCGGCAGCGGCGCG T C AL138752.2 Ensembl:ENSG00000255872 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:37753836..37753907;chr9:37753827..37753904 26863196 MeRIP-seq:(Medium) rs7848132 Functional Loss SNV dbSNP153 33..33 33 - - - 64379 RMVar_ID_64379 Human_SNP_ID_397831782 m1A Human chr9 - 37753849 37753849 37753849 CCAGCCCCCTTAACCAGCGGACAGCGTACCTGATCCCCTCACCCCCACGCAGCGGCAGCGGCGCG CCAGCCCCCTTAACCAGCGGACAGCGTACCTGCTCCCCTCACCCCCACGCAGCGGCAGCGGCGCG T G AL138752.2 Ensembl:ENSG00000255872 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:37753836..37753907;chr9:37753827..37753904 26863196 MeRIP-seq:(Medium) rs7848132 Functional Loss SNV dbSNP153 33..33 33 - - - 64380 RMVar_ID_64380 Human_SNP_ID_397834254 m1A Human chr9 + 37761967 37761967 37761967 GACTGGAAATTGGAAGGGAGTACTCAGAAAGTAGAGTCACCTGTGCTGCAGGGGCAAGAAGGCAT GACTGGAAATTGGAAGGGAGTACTCAGAAAGTGGAGTCACCTGTGCTGCAGGGGCAAGAAGGCAT A G TRMT10B Ensembl:ENSG00000165275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:37761917..37761988 26863196 MeRIP-seq:(Medium) rs925093676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5029174 Human_Splice_Rec_1044844,Human_Splice_Rec_1044856,Human_Splice_Rec_1044870,Human_Splice_Rec_1044886,Human_Splice_Rec_1044892,Human_Splice_Rec_1044898,Human_Splice_Rec_1044910,Human_Splice_Rec_1044926 RMVar_hsa_circ_59879,RMVar_hsa_circ_72600,RMVar_hsa_circ_344444,RMVar_hsa_circ_61949,RMVar_hsa_circ_256934 64381 RMVar_ID_64381 Human_SNP_ID_397839706 m1A Human chr9 - 37780721 37780721 37780721 AACATTTTAGAAGCTTGTGAACACATGACGTCAGATCAAAGAAAACAGATCTTCTCCAGATTGGC AACATTTTAGAAGCTTGTGAACACATGACGTCGGATCAAAGAAAACAGATCTTCTCCAGATTGGC T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37780671..37780771 32194978 MeRIP-seq:(Medium) rs760030050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2064754,Human_RBP_ID_9236631,Human_RBP_ID_16681172,Human_RBP_ID_24303601,Human_RBP_ID_27375517 RMVar_hsa_circ_53317,RMVar_hsa_circ_256941,RMVar_hsa_circ_256943 64382 RMVar_ID_64382 Human_SNP_ID_397839744 m1A Human chr9 - 37780820 37780820 37780820 CAGGAAGTGGGAAAACTCTATCCACTGGAGATAGTATTTGGAATGAATGGAAGAATATGGGTTAA CAGGAAGTGGGAAAACTCTATCCACTGGAGATGGTATTTGGAATGAATGGAAGAATATGGGTTAA T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:37780770..37780870 32194978 MeRIP-seq:(Medium) rs530072674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2064755,Human_RBP_ID_16681179,Human_RBP_ID_24303603 Human_Splice_Rec_1044944,Human_Splice_Rec_1044952,Human_Splice_Rec_1044956,Human_Splice_Rec_1044960,Human_Splice_Rec_1044966,Human_Splice_Rec_1044972 RMVar_hsa_circ_53317,RMVar_hsa_circ_256941,RMVar_hsa_circ_256943 64383 RMVar_ID_64383 Human_SNP_ID_397840647 m1A Human chr9 - 37784052 37784052 37784052 TCATTCTGTTTCTTTTTGTAGTATGTTCCAGTAAAAGGAGACCATGTGATTGGCATAGTGACAGC TCATTCTGTTTCTTTTTGTAGTATGTTCCAGTGAAAGGAGACCATGTGATTGGCATAGTGACAGC T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37784001..37784075 26863196 MeRIP-seq:(Medium) rs1459576809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5029201,Human_RBP_ID_18136324 Human_Splice_Rec_1044772,Human_Splice_Rec_1044942,Human_Splice_Rec_1044948,Human_Splice_Rec_1044954,Human_Splice_Rec_1044958,Human_Splice_Rec_1044962,Human_Splice_Rec_1044968,Human_Splice_Rec_1044974,Human_Splice_Rec_1044978 RMVar_hsa_circ_53317,RMVar_hsa_circ_256941,RMVar_hsa_circ_256943,RMVar_hsa_circ_307430,RMVar_hsa_circ_42197 64384 RMVar_ID_64384 Human_SNP_ID_397841010 m1A Human chr9 + 37785010 37785008 37785010 CTGTGCGTGCAGCGCGCGCCCTGCTGCCCGCGAGAGATTCAGCCGCGACAGACGCAGGTTCGGCC CTGTGCGTGCAGCGCGCGCCCTGCTGCCCGC__GAGATTCAGCCGCGACAGACGCAGGTTCGGCC CGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:37784701..37785075 26863196 MeRIP-seq:(Medium) rs1423492715 Functional Loss DEL dbSNP153 32..33 33 - - - 64385 RMVar_ID_64385 Human_SNP_ID_397841015 m1A Human chr9 + 37785010 37785010 37785010 CTGTGCGTGCAGCGCGCGCCCTGCTGCCCGCGAGAGATTCAGCCGCGACAGACGCAGGTTCGGCC CTGTGCGTGCAGCGCGCGCCCTGCTGCCCGCGGGAGATTCAGCCGCGACAGACGCAGGTTCGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:37784701..37785075 26863196 MeRIP-seq:(Medium) rs1447275667 Functional Loss SNV dbSNP153 33..33 33 - - - 64386 RMVar_ID_64386 Human_SNP_ID_397841057 m1A Human chr9 + 37785043 37785043 37785043 GAGATTCAGCCGCGACAGACGCAGGTTCGGCCATCGCGGGCTCCACCAAACACCGTTTCCGGTAC GAGATTCAGCCGCGACAGACGCAGGTTCGGCCGTCGCGGGCTCCACCAAACACCGTTTCCGGTAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:37784943..37785043 26863410 MeRIP-seq:(Medium) rs1325914775 Functional Loss SNV dbSNP153 33..33 33 - - - 64387 RMVar_ID_64387 Human_SNP_ID_397868523 m1A Human chr9 + 37904302 37904302 37904302 CCGCCGCGGCGGGGCAGGTAGAGGGCCACGCCAGCACACCTGTCAGGATGCGGGCTCCGCTAGCC CCGCCGCGGCGGGGCAGGTAGAGGGCCACGCCCGCACACCTGTCAGGATGCGGGCTCCGCTAGCC A C lnc-DCAF10-2,lnc-DCAF10-1,lnc-DCAF10-2:2 RNACentral:URS0000D5D639,RNACentral:URS00008B8DF0,RNACentral:URS0000D5A3BC lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr9:37904209..37904350;chr9:37904149..37904330 26863196 MeRIP-seq:(Medium) rs1303313424 Functional Loss SNV dbSNP153 33..33 33 - - - 64388 RMVar_ID_64388 Human_SNP_ID_397880124 m1A Human chr9 - 37948727 37948727 37948727 CACAGATGGTATCACGGAGCCATCAGCAGAGGAGACGCCGAGAACCTGCTGCGACTCTGCAAGGA CACAGATGGTATCACGGAGCCATCAGCAGAGGGGACGCCGAGAACCTGCTGCGACTCTGCAAGGA T C SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37948676..37948811 26863196 MeRIP-seq:(Medium) rs3827519 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1044766,Human_Splice_Rec_1044767,Human_Splice_Rec_1045040,Human_Splice_Rec_1045041 Human_miRNA_ID_2017795,Human_miRNA_ID_2221414,Human_miRNA_ID_2484466,Human_miRNA_ID_3072843 GWAS_ID_7867,GWAS_ID_7868,GWAS_ID_7869,GWAS_ID_7870,GWAS_ID_7871,GWAS_ID_7872,GWAS_ID_7873,GWAS_ID_7874 RMVar_hsa_circ_256957,RMVar_hsa_circ_297965,RMVar_hsa_circ_311485,RMVar_hsa_circ_256959,RMVar_hsa_circ_291058,RMVar_hsa_circ_256958 64389 RMVar_ID_64389 Human_SNP_ID_397886748 m1A Human chr9 - 37974727 37974727 37974727 AAAGTGTTGACTCAGACTCGGAGAGCACAGTCAGCCCCCGACTGCGGGAGAGCAAGCTGCCCCAG AAAGTGTTGACTCAGACTCGGAGAGCACAGTCGGCCCCCGACTGCGGGAGAGCAAGCTGCCCCAG T C SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37974676..38068315 26863196 MeRIP-seq:(Medium) rs1268770001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182813 RMVar_hsa_circ_256957,RMVar_hsa_circ_311485,RMVar_hsa_circ_291058,RMVar_hsa_circ_256958,RMVar_hsa_circ_306793,RMVar_hsa_circ_354519,RMVar_hsa_circ_367879,RMVar_hsa_circ_309307 64390 RMVar_ID_64390 Human_SNP_ID_397895769 m1A Human chr9 + 38010499 38010499 38010499 TCATTATCCCATCAAAAGCCTCATCTCCAGCCACTCCTCTCTAGCAACAAGGGCCCACCTCTATG TCATTATCCCATCAAAAGCCTCATCTCCAGCCGCTCCTCTCTAGCAACAAGGGCCCACCTCTATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:38010495..38010706 26863196 MeRIP-seq:(Medium) rs1283567099 Functional Loss SNV dbSNP153 33..33 33 - - - 64391 RMVar_ID_64391 Human_SNP_ID_397910779 m1A Human chr9 + 38068458 38068458 38068458 TGTCGTCGGGCAGCGAGCCCGAAGAGGCTGAGAAGCAGGAGGCGGTGGCCGGACCGCAGGACGCC TGTCGTCGGGCAGCGAGCCCGAAGAGGCTGAGTAGCAGGAGGCGGTGGCCGGACCGCAGGACGCC A T NONHSAG052191.2 RNACentral:URS00008C187A lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:38068407..38068658 26863196 MeRIP-seq:(Medium) rs769991852 Functional Loss SNV dbSNP153 33..33 33 - - - 64392 RMVar_ID_64392 Human_SNP_ID_397910787 m1A Human chr9 + 38068478 38068478 38068478 GAAGAGGCTGAGAAGCAGGAGGCGGTGGCCGGACCGCAGGACGCCGAGGCGGCGGAGGAGGCCTG GAAGAGGCTGAGAAGCAGGAGGCGGTGGCCGGCCCGCAGGACGCCGAGGCGGCGGAGGAGGCCTG A C NONHSAG052191.2 RNACentral:URS00008C187A lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:38068431..38068565 26863196 MeRIP-seq:(Medium) rs1241279635 Functional Loss SNV dbSNP153 33..33 33 - - - 64393 RMVar_ID_64393 Human_SNP_ID_397910788 m1A Human chr9 + 38068478 38068478 38068478 GAAGAGGCTGAGAAGCAGGAGGCGGTGGCCGGACCGCAGGACGCCGAGGCGGCGGAGGAGGCCTG GAAGAGGCTGAGAAGCAGGAGGCGGTGGCCGGGCCGCAGGACGCCGAGGCGGCGGAGGAGGCCTG A G NONHSAG052191.2 RNACentral:URS00008C187A lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:38068431..38068565 26863196 MeRIP-seq:(Medium) rs1241279635 Functional Loss SNV dbSNP153 33..33 33 - - - 64394 RMVar_ID_64394 Human_SNP_ID_397910912 m1A Human chr9 + 38068661 38068661 38068661 TTTAGCCACTTGGCCATGGCGAGAGGCCGCCTAGGGCCGCGGCGCGGGAGCCCGGTCCGCCGCCG TTTAGCCACTTGGCCATGGCGAGAGGCCGCCTGGGGCCGCGGCGCGGGAGCCCGGTCCGCCGCCG A G NONHSAG052191.2 RNACentral:URS00008C187A lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:38068622..38068751 26863196 MeRIP-seq:(Medium) rs754278102 Functional Loss SNV dbSNP153 33..33 33 - - - 64395 RMVar_ID_64395 Human_SNP_ID_397911126 m1A Human chr9 + 38069166 38069166 38069166 GCCGGGAGAGACAGCGAGCGACGGAGGAAGGCAGCCGGCGCCCGCCGGAGCCCGCGCGCCCGTGC GCCGGGAGAGACAGCGAGCGACGGAGGAAGGCGGCCGGCGCCCGCCGGAGCCCGCGCGCCCGTGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr9:38069076..38069250 26863410 MeRIP-seq:(Medium) rs1361496549 Functional Loss SNV dbSNP153 33..33 33 - - - 64396 RMVar_ID_64396 Human_SNP_ID_397913777 m1A Human chr9 + 38076934 38076934 38076934 AAGGAACAAACTCTGAACACACCGTCTTTAAGAACCGTAACATTCACCGCGAGAGTCCGCGGCTT AAGGAACAAACTCTGAACACACCGTCTTTAAGGACCGTAACATTCACCGCGAGAGTCCGCGGCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:38076813..38076996 26863196 MeRIP-seq:(Medium) rs1028834216 Functional Loss SNV dbSNP153 33..33 33 - - - 64397 RMVar_ID_64397 Human_SNP_ID_397991614 m1A Human chr9 + 38397034 38397034 38397034 TGGGCCTGTGCAGCCCCTGTTCAAGTTCAAGAAGATTGAGGAGGTGGTTGAGAGGGCCAACAACA TGGGCCTGTGCAGCCCCTGTTCAAGTTCAAGACGATTGAGGAGGTGGTTGAGAGGGCCAACAACA A C ALDH1B1 Ensembl:ENSG00000137124 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:38396986..38397115 26863196 MeRIP-seq:(Medium) rs773841295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7928547,Human_RBP_ID_18140802,Human_RBP_ID_27375623 Human_miRNA_ID_2015807 RMVar_hsa_circ_79529,RMVar_hsa_circ_88124,RMVar_hsa_circ_256964,RMVar_hsa_circ_256965 64398 RMVar_ID_64398 Human_SNP_ID_398026690 m1A Human chr9 + 38545636 38545636 38545636 CTCAATAACGTGCATTGCACCTGACATCTCCCAGCAGTGCTCAGCAGCCCCTGCTGACCAGGTCC CTCAATAACGTGCATTGCACCTGACATCTCCCCGCAGTGCTCAGCAGCCCCTGCTGACCAGGTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:38545494..38545819 26863196 MeRIP-seq:(Medium) rs999663871 Functional Loss SNV dbSNP153 33..33 33 - - - 64399 RMVar_ID_64399 Human_SNP_ID_398026691 m1A Human chr9 + 38545636 38545636 38545636 CTCAATAACGTGCATTGCACCTGACATCTCCCAGCAGTGCTCAGCAGCCCCTGCTGACCAGGTCC CTCAATAACGTGCATTGCACCTGACATCTCCCGGCAGTGCTCAGCAGCCCCTGCTGACCAGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:38545494..38545819 26863196 MeRIP-seq:(Medium) rs999663871 Functional Loss SNV dbSNP153 33..33 33 - - - 64400 RMVar_ID_64400 Human_SNP_ID_398026854 m1A Human chr9 + 38546234 38546234 38546234 TGACTGGGTCCCATGTGACCAGGCCTCCAATGAATAGCACCCCTTGAGCTGGTCACCAGTGACCC TGACTGGGTCCCATGTGACCAGGCCTCCAATGTATAGCACCCCTTGAGCTGGTCACCAGTGACCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:38546184..38546268 26863196 MeRIP-seq:(Medium) rs1413273580 Functional Loss SNV dbSNP153 33..33 33 - - - 64401 RMVar_ID_64401 Human_SNP_ID_398044364 m1A Human chr9 - 38620285 38620285 38620285 AGCGGGTGGTGGGCGTCTGAGAAGTCGCCACCATGAGGAAGCTCTTCAGCTTCGGGAGACGCCTG AGCGGGTGGTGGGCGTCTGAGAAGTCGCCACCCTGAGGAAGCTCTTCAGCTTCGGGAGACGCCTG T G ANKRD18A Ensembl:ENSG00000180071 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:38620235..38620331 26863196 MeRIP-seq:(Medium) rs1354456044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906829,Human_RBP_ID_5029674,Human_RBP_ID_9442645,Human_RBP_ID_21995831,Human_RBP_ID_22119816,Human_RBP_ID_27137057 64402 RMVar_ID_64402 Human_SNP_ID_398044626 m1A Human chr9 - 38621134 38621134 38621134 TGGCTAGAGGTCCCGAGCTTCAGCAGACGAGGAGCCGAGCAGGGGCAGGGCCTGGCGGGCTCTCA TGGCTAGAGGTCCCGAGCTTCAGCAGACGAGGGGCCGAGCAGGGGCAGGGCCTGGCGGGCTCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:38621117..38621258 26863196 MeRIP-seq:(Medium) rs1272453171 Functional Loss SNV dbSNP153 33..33 33 - - - 64403 RMVar_ID_64403 Human_SNP_ID_398382920 m1A Human chr9 - 40584240 40584240 40584240 GCGGACAGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCGCACAGCGGCGGAGAGGCGCACAGGGG GCGGACAGCGGCGGAGAGGCGGACAGCGGCGGCGAGGCGCACAGCGGCGGAGAGGCGCACAGGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:40584162..40584318;chr9:40584171..40584288 26863196 MeRIP-seq:(Medium) rs1429885553 Functional Loss SNV dbSNP153 33..33 33 - - - 64404 RMVar_ID_64404 Human_SNP_ID_398382943 m1A Human chr9 - 40584284 40584284 40584284 GCGGGCGGCGGCGGCGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCG GCGGGCGGCGGCGGCGCGGCGGAGAGGCGGACGGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:40584169..40584329 26863196 MeRIP-seq:(Medium) rs1438120426 Functional Loss SNV dbSNP153 33..33 33 - - - 64405 RMVar_ID_64405 Human_SNP_ID_398567496 m1A Human chr9 + 41055241 41055241 41055241 GAAGGAAAGAAAGAAAGGAAGGAAAGAAAGAAAGAAAGGAAAGAAAGAAAGGGAAAGAAAGAGAG GAAGGAAAGAAAGAAAGGAAGGAAAGAAAGAAGGAAAGGAAAGAAAGAAAGGGAAAGAAAGAGAG A G FRG1HP Ensembl:ENSG00000276291 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:41055212..41055318 26863196 MeRIP-seq:(Medium) rs1371763802 Functional Loss SNV dbSNP153 33..33 33 - - - 64406 RMVar_ID_64406 Human_SNP_ID_398575948 m1A Human chr9 + 41074723 41074722 41074723 CCCGCCCACCTTCTCCGCTGCCAGACCGCCCGAGGTGCCCTCAGTTTCTCCCCAAGTTGGACTCA CCCGCCCACCTTCTCCGCTGCCAGACCGCCCG_GGTGCCCTCAGTTTCTCCCCAAGTTGGACTCA GA G FRG1HP,BX255923.1 Ensembl:ENSG00000276291,Ensembl:ENSG00000225655 Pseudogene,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:41074531..41074885 26863196 MeRIP-seq:(Medium) rs1399267923 Functional Loss DEL dbSNP153 33..33 33 - - - 64407 RMVar_ID_64407 Human_SNP_ID_398628832 m1A Human chr9 - 41272090 41272090 41272090 TGTAGATTTGTAGTAGGCTGTGAAACTGAAAAATGTGAGTTTTCTAATATTCTTTTTCAAGACTG TGTAGATTTGTAGTAGGCTGTGAAACTGAAAACTGTGAGTTTTCTAATATTCTTTTTCAAGACTG T G AL845472.2 Ensembl:ENSG00000279561 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs199821637 Functional Loss SNV dbSNP153 33..33 33 - - - 64408 RMVar_ID_64408 Human_SNP_ID_398655716 m1A Human chr9 - 41358774 41358774 41358774 TAAAAAATGGCGGCGACGCGGCGGCTGCGGGGACTGGTGCGGCGGTGCTGGAGGTTGCGGCGGCG TAAAAAATGGCGGCGACGCGGCGGCTGCGGGGTCTGGTGCGGCGGTGCTGGAGGTTGCGGCGGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:41358724..41358794 26863196 MeRIP-seq:(Medium) rs1401999301 Functional Loss SNV dbSNP153 33..33 33 - - - 64409 RMVar_ID_64409 Human_SNP_ID_398755596 m1A Human chr9 + 41754619 41754602 41754619 GGACGAGATAGACACCGAGGCGGTGAAAATGGAGAGGCCATGTGAAGGTGGAAGGGACAGAATTT GGACGAGATAGACACC_________________GAGGCCATGTGAAGGTGGAAGGGACAGAATTT CGAGGCGGTGAAAATGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:41754497..41754618 26863196 MeRIP-seq:(Medium) rs1418674552 Functional Loss DEL dbSNP153 17..33 33 - - - 64410 RMVar_ID_64410 Human_SNP_ID_399101410 m1A Human chr9 - 42900367 42900367 42900367 CCTTTCTATTCCTCTGACCCCGCCTCCTTTCTAAATGCAGCGACCTCTGTTCTTCAGCCCTATCC CCTTTCTATTCCTCTGACCCCGCCTCCTTTCTCAATGCAGCGACCTCTGTTCTTCAGCCCTATCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:42900324..42900425 26863196 MeRIP-seq:(Medium) rs913935204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21729732 64411 RMVar_ID_64411 Human_SNP_ID_642498935 m1A Human chr18 + 31102339 31102339 31102339 AAGGTGTTTCTCACCAGCGGACGCCACCTATAAGGCCCATCTCCCCCACCACGCCCCGGTGTCCG AAGGTGTTTCTCACCAGCGGACGCCACCTATACGGCCCATCTCCCCCACCACGCCCCGGTGTCCG A C DSCAS Ensembl:ENSG00000265888 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:31102288..31102398 26863196 MeRIP-seq:(Medium) rs1055513293 Functional Loss SNV dbSNP153 33..33 33 - - - 64412 RMVar_ID_64412 Human_SNP_ID_642599154 m1A Human chr18 - 31498248 31498248 31498248 GCGTACGCGCGTCCCGGGCTCCGCGCCATCGCACCCTCGCCTCCGCCTCCCGCCGCCGCACCGCT GCGTACGCGCGTCCCGGGCTCCGCGCCATCGCCCCCTCGCCTCCGCCTCCCGCCGCCGCACCGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:31498069..31498338;chr18:31498064..31519862 26863196 MeRIP-seq:(Medium) rs886053711 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_252 64413 RMVar_ID_64413 Human_SNP_ID_642603713 m1A Human chr18 - 31518240 31518240 31518240 GTAAGTGAAGTCCACTTCCAACGTTAAAGCAGATCTGTAAAATAAAATTATTTGATATTTAGCCA GTAAGTGAAGTCCACTTCCAACGTTAAAGCAGGTCTGTAAAATAAAATTATTTGATATTTAGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:31518226..31518275 26863196 MeRIP-seq:(Medium) rs1478351535 Functional Loss SNV dbSNP153 33..33 33 - - - 64414 RMVar_ID_64414 Human_SNP_ID_642603714 m1A Human chr18 - 31518246 31518246 31518246 TCACCTGTAAGTGAAGTCCACTTCCAACGTTAAAGCAGATCTGTAAAATAAAATTATTTGATATT TCACCTGTAAGTGAAGTCCACTTCCAACGTTACAGCAGATCTGTAAAATAAAATTATTTGATATT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:31518226..31518300 26863410 MeRIP-seq:(Medium) rs960627545 Functional Loss SNV dbSNP153 33..33 33 - - - 64415 RMVar_ID_64415 Human_SNP_ID_642604008 m1A Human chr18 - 31519730 31519726 31519731 AAATATAGAACATTAGTATGCTGTCCTATAACATAATAAACTTTTAAATAGTGCAAATTTTAAGG AAATATAGAACATTAGTATGCTGTCCTATAA_____TAAACTTTTAAATAGTGCAAATTTTAAGG ATTATG A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:31519728..31519825 26863410 MeRIP-seq:(Medium) rs912860902 Functional Loss DEL dbSNP153 32..36 33 - - - 64416 RMVar_ID_64416 Human_SNP_ID_642604016 m1A Human chr18 - 31519758 31519758 31519758 AATATTGCCAAAATTTATTATGTGTCATAAATATAGAACATTAGTATGCTGTCCTATAACATAAT AATATTGCCAAAATTTATTATGTGTCATAAATGTAGAACATTAGTATGCTGTCCTATAACATAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:31519756..31519825 26863196 MeRIP-seq:(Medium) rs1485852686 Functional Loss SNV dbSNP153 33..33 33 - - - 64417 RMVar_ID_64417 Human_SNP_ID_642636012 m1A Human chr18 + 31652104 31652104 31652104 TTCTCTCCATCCTTTCTTTCCATGATGCCTACAACATGCTCAAGTCCATCTCTTCCTAAAGAGCT TTCTCTCCATCCTTTCTTTCCATGATGCCTACGACATGCTCAAGTCCATCTCTTCCTAAAGAGCT A G RF00017-1725 RNACentral:URS0000915249 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:31652100..31652223 26863196 MeRIP-seq:(Medium) rs1224440422 Functional Loss SNV dbSNP153 33..33 33 - - - 64418 RMVar_ID_64418 Human_SNP_ID_642678647 m1A Human chr18 + 31833488 31833487 31833488 TCCTGCCAATTCTCTCACCCACACATCTCTGGAACCTGGTTACTTCACTGTATCTCATTTTCCTT TCCTGCCAATTCTCTCACCCACACATCTCTGG_ACCTGGTTACTTCACTGTATCTCATTTTCCTT GA G RF00017-1725 RNACentral:URS0000915249 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:31833449..31833545 26863196 MeRIP-seq:(Medium) rs1368772337 Functional Loss DEL dbSNP153 33..33 33 - - - 64419 RMVar_ID_64419 Human_SNP_ID_642679017 m1A Human chr18 + 31834850 31834850 31834850 CATGACCAAACCTCCTACTGTCCCATTTCCTCACATTTCTACTTGTTTTCTGAAACCCCCATTAA CATGACCAAACCTCCTACTGTCCCATTTCCTCGCATTTCTACTTGTTTTCTGAAACCCCCATTAA A G RF00017-1725 RNACentral:URS0000915249 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:31834800..31834942 26863196 MeRIP-seq:(Medium) rs1275374936 Functional Loss SNV dbSNP153 33..33 33 - - - 64420 RMVar_ID_64420 Human_SNP_ID_642680071 m1A Human chr18 - 31838582 31838582 31838582 AATAGCATGACATCATAGGTTGAGAAGCAAATAGGAGGTAAGAAAGTAAAGATACCGCGTTGACC AATAGCATGACATCATAGGTTGAGAAGCAAATCGGAGGTAAGAAAGTAAAGATACCGCGTTGACC T G TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:31838521..31838619 26863196 MeRIP-seq:(Medium) rs1177918957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13280699,Human_RBP_ID_23765828 RMVar_hsa_circ_55770,RMVar_hsa_circ_271277,RMVar_hsa_circ_329478,RMVar_hsa_circ_189418,RMVar_hsa_circ_345867,RMVar_hsa_circ_300636,RMVar_hsa_circ_97025,RMVar_hsa_circ_103717,RMVar_hsa_circ_80710,RMVar_hsa_circ_189419,RMVar_hsa_circ_189421,RMVar_hsa_circ_189423,RMVar_hsa_circ_3461,RMVar_hsa_circ_189424,RMVar_hsa_circ_189422,RMVar_hsa_circ_189420 64421 RMVar_ID_64421 Human_SNP_ID_642709065 m1A Human chr18 - 31942858 31942858 31942858 CCAGTGCGTTCGGGGCCCCGCCCGGCCGGGCCAGGCCGGCGGGCGGCGGCGGTAGCTGCTGCAGC CCAGTGCGTTCGGGGCCCCGCCCGGCCGGGCCGGGCCGGCGGGCGGCGGCGGTAGCTGCTGCAGC T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:31942772..31942871 26863410 MeRIP-seq:(Medium) rs1366222121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238650,Human_RBP_ID_905506,Human_RBP_ID_9327744,Human_RBP_ID_18993366,Human_RBP_ID_22589454,Human_RBP_ID_22660979,Human_RBP_ID_22741207,Human_RBP_ID_24559606,Human_RBP_ID_25376898 Human_Splice_Rec_1903206 RMVar_hsa_circ_17655,RMVar_hsa_circ_81999,RMVar_hsa_circ_66509,RMVar_hsa_circ_189450,RMVar_hsa_circ_351786,RMVar_hsa_circ_353544,RMVar_hsa_circ_189472,RMVar_hsa_circ_57428 64422 RMVar_ID_64422 Human_SNP_ID_642709122 m1A Human chr18 - 31942965 31942958 31942965 CACGCGGGGACGAGCGCTGAGAAGCGGCGGTGACGGGAAGGGGGGGGTCAGTGGATTGTGCCCCA CACGCGGGGACGAGCGCTGAGAAGCGGCGGTG_______GGGGGGGGTCAGTGGATTGTGCCCCA CTTCCCGT C TRAPPC8 Ensembl:ENSG00000153339 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:31942865..31943123 26863196 MeRIP-seq:(Medium) rs373028465 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_51856,Human_RBP_ID_768853,Human_RBP_ID_4495524,Human_RBP_ID_18993367,Human_RBP_ID_19087596,Human_RBP_ID_21976839,Human_RBP_ID_22661099 Human_Splice_Rec_1903267 RMVar_hsa_circ_81999,RMVar_hsa_circ_189450 64423 RMVar_ID_64423 Human_SNP_ID_642709159 m1A Human chr18 - 31943064 31943064 31943064 TCAACATGGCGGTTCCGGCCGGGCAGTGACCAAGGTTTTGCCGTCCGAAGGACTAAGTGGTGACT TCAACATGGCGGTTCCGGCCGGGCAGTGACCAGGGTTTTGCCGTCCGAAGGACTAAGTGGTGACT T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:31942865..31943123;chr18:31942750..31943132 26863196 MeRIP-seq:(Medium) rs1317437971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823427,Human_RBP_ID_4494179,Human_RBP_ID_9290984,Human_RBP_ID_9327860,Human_RBP_ID_18420659,Human_RBP_ID_18715957,Human_RBP_ID_19087198,Human_RBP_ID_22965662,Human_RBP_ID_27814565,Human_RBP_ID_27838926 RMVar_hsa_circ_81999,RMVar_hsa_circ_189450 64424 RMVar_ID_64424 Human_SNP_ID_642746568 m1A Human chr18 + 32092000 32092000 32092000 CGGTGACGGCCGGGTAGGCTGTAGGCAGCGCAATGCCAAGACAGAGCTGCTGGCGGCGGCGGGCG CGGTGACGGCCGGGTAGGCTGTAGGCAGCGCACTGCCAAGACAGAGCTGCTGGCGGCGGCGGGCG A C RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:32091898..32092086 26863196 MeRIP-seq:(Medium) rs1414623124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136012,Human_RBP_ID_4486037,Human_RBP_ID_5585007,Human_RBP_ID_8194648 64425 RMVar_ID_64425 Human_SNP_ID_642746569 m1A Human chr18 + 32092000 32092000 32092000 CGGTGACGGCCGGGTAGGCTGTAGGCAGCGCAATGCCAAGACAGAGCTGCTGGCGGCGGCGGGCG CGGTGACGGCCGGGTAGGCTGTAGGCAGCGCAGTGCCAAGACAGAGCTGCTGGCGGCGGCGGGCG A G RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:32091898..32092086 26863196 MeRIP-seq:(Medium) rs1414623124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136012,Human_RBP_ID_4486037,Human_RBP_ID_5585007,Human_RBP_ID_8194648 64426 RMVar_ID_64426 Human_SNP_ID_642746981 m1A Human chr18 - 32092758 32092758 32092758 AGGTCCTCGGCCATGGCGGGGGATGGGGAAACAAGGCGATGGCGACAGCGGCAGCGGCCGAGGTG AGGTCCTCGGCCATGGCGGGGGATGGGGAAACCAGGCGATGGCGACAGCGGCAGCGGCCGAGGTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:32092710..32092833 26863196 MeRIP-seq:(Medium) rs1200671758 Functional Loss SNV dbSNP153 33..33 33 - - - 64427 RMVar_ID_64427 Human_SNP_ID_642749430 m1A Human chr18 - 32101013 32101013 32101013 CAGCAACAATATCACTTCCTAAAGAAAGGGTCATCGATACTCACCCACTAGATCTGATCCCTCTC CAGCAACAATATCACTTCCTAAAGAAAGGGTCGTCGATACTCACCCACTAGATCTGATCCCTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:32101011..32101145 26863196 MeRIP-seq:(Medium) rs1568226504 Functional Loss SNV dbSNP153 33..33 33 - - - 64428 RMVar_ID_64428 Human_SNP_ID_642794847 m1A Human chr18 - 32287541 32287541 32287541 GCTGTCCGTGATGTGAAAACCGACTGGAATGAAGAATGCAAGAGCCCCAAGAAGGGTCGGTGCTC GCTGTCCGTGATGTGAAAACCGACTGGAATGAGGAATGCAAGAGCCCCAAGAAGGGTCGGTGCTC T C GAREM1 Ensembl:ENSG00000141441 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs16962977 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6680327 GWAS_ID_7875,GWAS_ID_7876,GWAS_ID_7877 RMVar_hsa_circ_189505,RMVar_hsa_circ_39701,RMVar_hsa_circ_361928,RMVar_hsa_circ_189503,RMVar_hsa_circ_75394,RMVar_hsa_circ_324248,RMVar_hsa_circ_324757,RMVar_hsa_circ_189506,RMVar_hsa_circ_189504 64429 RMVar_ID_64429 Human_SNP_ID_642837687 m1A Human chr18 - 32470767 32470767 32470767 AGAGGAGGAGGAGGCGAGCGGGCGGCCGCCGCAGCTGCAGACCCAGGGCCAGAGGAGGAGGCGGA AGAGGAGGAGGAGGCGAGCGGGCGGCCGCCGCCGCTGCAGACCCAGGGCCAGAGGAGGAGGCGGA T G GAREM1 Ensembl:ENSG00000141441 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:32470747..32470858 26863196 MeRIP-seq:(Medium) rs1381150343 Functional Loss SNV dbSNP153 33..33 33 - - - 64430 RMVar_ID_64430 Human_SNP_ID_643097947 m1A Human chr18 + 33578500 33578464 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG _________________________________CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1235218925 Functional Loss DEL dbSNP153 1..33 33 - - - 64431 RMVar_ID_64431 Human_SNP_ID_643097956 m1A Human chr18 + 33578500 33578479 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCG_____________________CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCGCCGCCGCCGCCGCCGCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1466562115 Functional Loss DEL dbSNP153 13..33 33 - - - 64432 RMVar_ID_64432 Human_SNP_ID_643097961 m1A Human chr18 + 33578500 33578488 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCG____________CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCGCCGCCGCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1410644102 Functional Loss DEL dbSNP153 22..33 33 - - - 64433 RMVar_ID_64433 Human_SNP_ID_643097966 m1A Human chr18 + 33578500 33578491 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCG_________CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCGCCGCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1410781329 Functional Loss DEL dbSNP153 25..33 33 - - - 64434 RMVar_ID_64434 Human_SNP_ID_643097971 m1A Human chr18 + 33578500 33578494 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCGCCG______CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCGCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1249097476 Functional Loss DEL dbSNP153 28..33 33 - - - 64435 RMVar_ID_64435 Human_SNP_ID_643097979 m1A Human chr18 + 33578500 33578497 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCG___CCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG GCCA G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs1307553575 Functional Loss DEL dbSNP153 31..33 33 - - - 64436 RMVar_ID_64436 Human_SNP_ID_643097981 m1A Human chr18 + 33578500 33578500 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG A C ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs886248776 Functional Loss SNV dbSNP153 33..33 33 - - - 64437 RMVar_ID_64437 Human_SNP_ID_643097982 m1A Human chr18 + 33578500 33578500 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG A G ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs886248776 Functional Loss SNV dbSNP153 33..33 33 - - - 64438 RMVar_ID_64438 Human_SNP_ID_643097983 m1A Human chr18 + 33578500 33578500 33578500 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCCGCGCGCCTCCCCCCGCGGAGCGAGTG A T ASXL3 Ensembl:ENSG00000141431 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr18:33578434..33578526;chr18:33578451..33578587;chr18:33578385..33578583 26863196 MeRIP-seq:(Medium) rs886248776 Functional Loss SNV dbSNP153 33..33 33 - - - 64439 RMVar_ID_64439 Human_SNP_ID_643158298 m1A Human chr18 + 33820577 33820577 33820577 CGGCGCCCACCCGGAACCCGCGCCGGCCCGGGAGCGCCGCGCAGCCCGGGCTCCCGCCCGTGCCT CGGCGCCCACCCGGAACCCGCGCCGGCCCGGGCGCGCCGCGCAGCCCGGGCTCCCGCCCGTGCCT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:33820509..33820594 26863410 MeRIP-seq:(Medium) rs1396954378 Functional Loss SNV dbSNP153 33..33 33 - - - 64440 RMVar_ID_64440 Human_SNP_ID_643158299 m1A Human chr18 + 33820577 33820577 33820577 CGGCGCCCACCCGGAACCCGCGCCGGCCCGGGAGCGCCGCGCAGCCCGGGCTCCCGCCCGTGCCT CGGCGCCCACCCGGAACCCGCGCCGGCCCGGGTGCGCCGCGCAGCCCGGGCTCCCGCCCGTGCCT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:33820509..33820594 26863410 MeRIP-seq:(Medium) rs1396954378 Functional Loss SNV dbSNP153 33..33 33 - - - 64441 RMVar_ID_64441 Human_SNP_ID_643449848 m1A Human chr18 + 35041481 35041481 35041481 CGTGCGGAGCAGGCGAGCGAGCGGGAAGACGCAGCCACCTTCCTCACCAGCCAGCCCACAGCGGT CGTGCGGAGCAGGCGAGCGAGCGGGAAGACGCCGCCACCTTCCTCACCAGCCAGCCCACAGCGGT A C MAPRE2 Ensembl:ENSG00000166974 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:35041430..35041563 26863196 MeRIP-seq:(Medium) rs1245025968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494181,Human_RBP_ID_5319598,Human_RBP_ID_8828878,Human_RBP_ID_9290985,Human_RBP_ID_9327749,Human_RBP_ID_22446167 Human_miRNA_ID_2052614 RMVar_hsa_circ_62149,RMVar_hsa_circ_122723,RMVar_hsa_circ_117421,RMVar_hsa_circ_189585,RMVar_hsa_circ_77212,RMVar_hsa_circ_189586,RMVar_hsa_circ_189587 64442 RMVar_ID_64442 Human_SNP_ID_643449851 m1A Human chr18 + 35041485 35041485 35041485 CGGAGCAGGCGAGCGAGCGGGAAGACGCAGCCACCTTCCTCACCAGCCAGCCCACAGCGGTTTGT CGGAGCAGGCGAGCGAGCGGGAAGACGCAGCCGCCTTCCTCACCAGCCAGCCCACAGCGGTTTGT A G MAPRE2 Ensembl:ENSG00000166974 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:35041434..35041550 26863196 MeRIP-seq:(Medium) rs1385794083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011780,Human_RBP_ID_4494181,Human_RBP_ID_5319598,Human_RBP_ID_5498418,Human_RBP_ID_8828878,Human_RBP_ID_9290985,Human_RBP_ID_9327749,Human_RBP_ID_22446167 Human_miRNA_ID_2052614,Human_miRNA_ID_2333138,Human_miRNA_ID_2966220 RMVar_hsa_circ_62149,RMVar_hsa_circ_122723,RMVar_hsa_circ_117421,RMVar_hsa_circ_189585,RMVar_hsa_circ_77212,RMVar_hsa_circ_189586,RMVar_hsa_circ_189587 64443 RMVar_ID_64443 Human_SNP_ID_643520153 m1A Human chr18 + 35344409 35344409 35344409 TCAGGAACCGCAGCAGCTTCGCTGTCCACGGCAGACGCAGAAACGCCGTTCACAAGCCTTTTCCC TCAGGAACCGCAGCAGCTTCGCTGTCCACGGCCGACGCAGAAACGCCGTTCACAAGCCTTTTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:35344103..35344420 26863196 MeRIP-seq:(Medium) rs1350660693 Functional Loss SNV dbSNP153 33..33 33 - - - 64444 RMVar_ID_64444 Human_SNP_ID_643520158 m1A Human chr18 + 35344419 35344419 35344419 CAGCAGCTTCGCTGTCCACGGCAGACGCAGAAACGCCGTTCACAAGCCTTTTCCCAGAAGCCCCC CAGCAGCTTCGCTGTCCACGGCAGACGCAGAAGCGCCGTTCACAAGCCTTTTCCCAGAAGCCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:35344316..35344423 26863196 MeRIP-seq:(Medium) rs1005511170 Functional Loss SNV dbSNP153 33..33 33 - - - 64445 RMVar_ID_64445 Human_SNP_ID_643551115 m1A Human chr18 - 35480554 35480554 35480554 AACTATTTTTATTATGTTTTAAGGGTATCAGCATGGAAGCCATGAGTGAGAATAAAATGGTGCCC AACTATTTTTATTATGTTTTAAGGGTATCAGCCTGGAAGCCATGAGTGAGAATAAAATGGTGCCC T G AC007998.2,INO80C Ensembl:ENSG00000267140,Ensembl:ENSG00000153391 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:35480505..35480605 26863196 MeRIP-seq:(Medium) rs1240709516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23767750 Human_Splice_Rec_1905372,Human_Splice_Rec_1905380,Human_Splice_Rec_1905394,Human_Splice_Rec_1905402,Human_Splice_Rec_1905414,Human_Splice_Rec_1905422,Human_Splice_Rec_1905430,Human_Splice_Rec_1905431,Human_Splice_Rec_1905436 RMVar_hsa_circ_189602,RMVar_hsa_circ_189601,RMVar_hsa_circ_123530,RMVar_hsa_circ_89785,RMVar_hsa_circ_108689,RMVar_hsa_circ_189604,RMVar_hsa_circ_279213,RMVar_hsa_circ_189605 64446 RMVar_ID_64446 Human_SNP_ID_643575372 m1A Human chr18 + 35581371 35581371 35581371 GGAGGGGCGCCGCGCCCGACCCCGGAGTCCCGAGCCCGAGGGGAGCGTCGCGGCCCCGCGGTGGG GGAGGGGCGCCGCGCCCGACCCCGGAGTCCCGGGCCCGAGGGGAGCGTCGCGGCCCCGCGGTGGG A G GALNT1 Ensembl:ENSG00000141429 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:35581111..35581473 26863196 MeRIP-seq:(Medium) rs1368730053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4493989 64447 RMVar_ID_64447 Human_SNP_ID_643578482 m1A Human chr18 + 35594292 35594292 35594292 CAAATAAAGAGTATTATCCTTAAAAAGGAGAAAAAACTCAGAGGAACAAGGGAGTGTGAGGTAAA CAAATAAAGAGTATTATCCTTAAAAAGGAGAAGAAACTCAGAGGAACAAGGGAGTGTGAGGTAAA A G GALNT1 Ensembl:ENSG00000141429 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:35594290..35594493 26863196 MeRIP-seq:(Medium) rs937206349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82035,RMVar_hsa_circ_189606 64448 RMVar_ID_64448 Human_SNP_ID_643591265 m1A Human chr18 - 35647040 35647040 35647040 GATGAAGCTGGAGATGATAAAAGTGGGAAGATACAAGAGATACGATGGGACAAACTCAATCCTAG GATGAAGCTGGAGATGATAAAAGTGGGAAGATGCAAGAGATACGATGGGACAAACTCAATCCTAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:35646912..35647039 26863196 MeRIP-seq:(Medium) rs575075266 Functional Loss SNV dbSNP153 33..33 33 - - - 64449 RMVar_ID_64449 Human_SNP_ID_643599436 m1A Human chr18 - 35683593 35683593 35683593 GCAAACTTACAGACACCAGAAAATTACCTGTCATGTTTGATCCTGGCCAAGAGAGGCTCCAGCCA GCAAACTTACAGACACCAGAAAATTACCTGTCGTGTTTGATCCTGGCCAAGAGAGGCTCCAGCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:35683468..35683642 32194978 MeRIP-seq:(Medium) rs1311508682 Functional Loss SNV dbSNP153 33..33 33 - - - 64450 RMVar_ID_64450 Human_SNP_ID_643602272 m1A Human chr18 + 35695394 35695393 35695394 GGAAACTGGCAGTTTGTGGTGGAAGTGTGAGGACCTTCTCTTCTGGTGGCTTGTTTCCTCAGTTG GGAAACTGGCAGTTTGTGGTGGAAGTGTGAGG_CCTTCTCTTCTGGTGGCTTGTTTCCTCAGTTG GA G GALNT1 Ensembl:ENSG00000141429 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:35695357..35695457 26863196 MeRIP-seq:(Medium) rs536160961 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_953,RMVar_hsa_circ_189610,RMVar_hsa_circ_372425,RMVar_hsa_circ_189612,RMVar_hsa_circ_189613,RMVar_hsa_circ_292725,RMVar_hsa_circ_189615,RMVar_hsa_circ_114348 64451 RMVar_ID_64451 Human_SNP_ID_643671847 m1A Human chr18 - 35972744 35972744 35972744 GTCGTGCAGTCCCCGCGCTGCAGCCTCAAGGTAGTGCTTCTGTCTCATCGCCGCCGCCGCTGCCG GTCGTGCAGTCCCCGCGCTGCAGCCTCAAGGTTGTGCTTCTGTCTCATCGCCGCCGCCGCTGCCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:35972676..35972898 26863196 MeRIP-seq:(Medium) rs1158609875 Functional Loss SNV dbSNP153 33..33 33 - - - 64452 RMVar_ID_64452 Human_SNP_ID_643671862 m1A Human chr18 + 35972772 35972772 35972772 GCACTACCTTGAGGCTGCAGCGCGGGGACTGCACGACAGCTGCCCGGGCCAAGCCCGCTACCTCC GCACTACCTTGAGGCTGCAGCGCGGGGACTGCGCGACAGCTGCCCGGGCCAAGCCCGCTACCTCC A G C18orf21,AC091060.1 Ensembl:ENSG00000141428,Ensembl:ENSG00000278986 Protein coding,Other 5'UTR,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:35972723..35972856 26863196 MeRIP-seq:(Medium) rs1395543849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238690,Human_RBP_ID_906163,Human_RBP_ID_4486797,Human_RBP_ID_5190303,Human_RBP_ID_5583774,Human_RBP_ID_5649448,Human_RBP_ID_6712586,Human_RBP_ID_18993658,Human_RBP_ID_26814398 Human_Splice_Rec_1905517,Human_Splice_Rec_1905523,Human_Splice_Rec_1905529,Human_Splice_Rec_1905535,Human_Splice_Rec_1905543,Human_Splice_Rec_1905551 Human_miRNA_ID_3196519,Human_miRNA_ID_3196535,Human_miRNA_ID_3196551 64453 RMVar_ID_64453 Human_SNP_ID_643673081 m1A Human chr18 + 35977482 35977482 35977482 ATGGTAAAAGTAGAAGCTTTGTGTCAACATTGAAGAGCAATCCTGCCACTCCTACAAGTAAACTC ATGGTAAAAGTAGAAGCTTTGTGTCAACATTGGAGAGCAATCCTGCCACTCCTACAAGTAAACTC A G C18orf21 Ensembl:ENSG00000141428 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs748172036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_507844,Human_RBP_ID_1549527,Human_RBP_ID_3554532,Human_RBP_ID_6682889,Human_RBP_ID_9379584,Human_RBP_ID_13293978,Human_RBP_ID_17266026 Human_Splice_Rec_1905520,Human_Splice_Rec_1905532,Human_Splice_Rec_1905540,Human_Splice_Rec_1905548,Human_Splice_Rec_1905556 RMVar_hsa_circ_377887 64454 RMVar_ID_64454 Human_SNP_ID_643677811 m1A Human chr18 + 35998454 35998450 35998454 TTTGGGAACCAATGCTTTACCTCATTCTTCTTACTCTGTTGACCGAAGCCACTTTACTTCTTCTC TTTGGGAACCAATGCTTTACCTCATTCTT____CTCTGTTGACCGAAGCCACTTTACTTCTTCTC TCTTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:35998450..35998569 26863196 MeRIP-seq:(Medium) rs1018171645 Functional Loss DEL dbSNP153 30..33 33 - - - 64455 RMVar_ID_64455 Human_SNP_ID_643711007 m1A Human chr18 - 36124627 36124627 36124627 CATCCAGGTTCCGCTGAATGCAACAGAGTTCAACTATCTCTGTCCAGCCATCATCAACCAAATTG CATCCAGGTTCCGCTGAATGCAACAGAGTTCAGCTATCTCTGTCCAGCCATCATCAACCAAATTG T C SLC39A6 Ensembl:ENSG00000141424 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs764123003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27461258 Human_Splice_Rec_1905660,Human_Splice_Rec_1905678,Human_Splice_Rec_1905694 RMVar_hsa_circ_123576,RMVar_hsa_circ_88455,RMVar_hsa_circ_189629,RMVar_hsa_circ_189630,RMVar_hsa_circ_189637,RMVar_hsa_circ_281676,RMVar_hsa_circ_189638,RMVar_hsa_circ_308085,RMVar_hsa_circ_36206,RMVar_hsa_circ_189641,RMVar_hsa_circ_293424,RMVar_hsa_circ_189642,RMVar_hsa_circ_272694,RMVar_hsa_circ_318654,RMVar_hsa_circ_189643 64456 RMVar_ID_64456 Human_SNP_ID_643712307 m1A Human chr18 + 36129215 36129215 36129215 GGGCTCGGAACGGGCCCACTGGTGTCTTCGAGAAATCTCTACCAGGCGCGAACACGCGGTGGTTT GGGCTCGGAACGGGCCCACTGGTGTCTTCGAGGAATCTCTACCAGGCGCGAACACGCGGTGGTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:36129083..36129325 26863196 MeRIP-seq:(Medium) rs1343767766 Functional Loss SNV dbSNP153 33..33 33 - - - 64457 RMVar_ID_64457 Human_SNP_ID_643713485 m1A Human chr18 + 36132967 36132962 36132967 GAAAAGGATGTGGGCACTGTAGGAGAGTGAGCAGAAGCAGGTGGGTGGATGCAGACGCGAGAGCT GAAAAGGATGTGGGCACTGTAGGAGAGT_____GAAGCAGGTGGGTGGATGCAGACGCGAGAGCT TGAGCA T ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:36132921..36133051 26863196 MeRIP-seq:(Medium) rs1248754518 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_5189728,Human_RBP_ID_6683456,Human_RBP_ID_13297040 64458 RMVar_ID_64458 Human_SNP_ID_643714840 m1A Human chr18 + 36138363 36138363 36138363 ACCAGAGGAGGACATCAGATCCTGCATTATGTACACTGATCGTTTCTGCAGCTGCAGATTCTGCT ACCAGAGGAGGACATCAGATCCTGCATTATGTCCACTGATCGTTTCTGCAGCTGCAGATTCTGCT A C ELP2 Ensembl:ENSG00000134759 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1785934 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_905511,Human_RBP_ID_5189222,Human_RBP_ID_18716537,Human_RBP_ID_18993660,Human_RBP_ID_22445880,Human_RBP_ID_22965668 Human_Splice_Rec_1905720,Human_Splice_Rec_1905721,Human_Splice_Rec_1905730,Human_Splice_Rec_1905731,Human_Splice_Rec_1905740,Human_Splice_Rec_1905741,Human_Splice_Rec_1905782,Human_Splice_Rec_1905783,Human_Splice_Rec_1905794,Human_Splice_Rec_1905795,Human_Splice_Rec_1905838,Human_Splice_Rec_1905839,Human_Splice_Rec_1905874,Human_Splice_Rec_1905875,Human_Splice_Rec_1905916,Human_Splice_Rec_1905917,Human_Splice_Rec_1905958,Human_Splice_Rec_1905964,Human_Splice_Rec_1905965,Human_Splice_Rec_1905972,Human_Splice_Rec_1905973,Human_Splice_Rec_1905984,Human_Splice_Rec_1905985,Human_Splice_Rec_1906024,Human_Splice_Rec_1906025,Human_Splice_Rec_1906066,Human_Splice_Rec_1906067,Human_Splice_Rec_1906076,Human_Splice_Rec_1906077,Human_Splice_Rec_1906085 Human_miRNA_ID_2730250,Human_miRNA_ID_2769326 GWAS_ID_7878,GWAS_ID_7879,GWAS_ID_7880 RMVar_hsa_circ_2640,RMVar_hsa_circ_109972,RMVar_hsa_circ_334505,RMVar_hsa_circ_340301,RMVar_hsa_circ_368254,RMVar_hsa_circ_39164,RMVar_hsa_circ_189644,RMVar_hsa_circ_189645,RMVar_hsa_circ_189646,RMVar_hsa_circ_40813,RMVar_hsa_circ_189647 64459 RMVar_ID_64459 Human_SNP_ID_643726282 m1A Human chr18 - 36182946 36182946 36182946 TCATGCCACAGGTGGGAAAGTTCAGTTAGAGAAGTGGGGACAGAGCCAGAAGAGAGCACCTTGGC TCATGCCACAGGTGGGAAAGTTCAGTTAGAGAGGTGGGGACAGAGCCAGAAGAGAGCACCTTGGC T C AC023043.1 Ensembl:ENSG00000260552 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:36182933..36183108 26863196 MeRIP-seq:(Medium) rs752085073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585030 64460 RMVar_ID_64460 Human_SNP_ID_643727438 m1A Human chr18 - 36187333 36187331 36187334 TGGGCGCGGGAGCGGGTGCCAGTCTTTAAACAACCTCTCGATGGGTCCCACGAAGATGTTTCCAG TGGGCGCGGGAGCGGGTGCCAGTCTTTAAAC___CTCTCGATGGGTCCCACGAAGATGTTTCCAG GGTT G AC023043.1 Ensembl:ENSG00000260552 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:36187113..36187400 26863196 MeRIP-seq:(Medium) rs986184319 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_508301 Human_Splice_Rec_1906165 64461 RMVar_ID_64461 Human_SNP_ID_643727439 m1A Human chr18 - 36187333 36187333 36187333 TGGGCGCGGGAGCGGGTGCCAGTCTTTAAACAACCTCTCGATGGGTCCCACGAAGATGTTTCCAG TGGGCGCGGGAGCGGGTGCCAGTCTTTAAACAGCCTCTCGATGGGTCCCACGAAGATGTTTCCAG T C AC023043.1 Ensembl:ENSG00000260552 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:36187113..36187400 26863196 MeRIP-seq:(Medium) rs1270148967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508301 Human_Splice_Rec_1906165 64462 RMVar_ID_64462 Human_SNP_ID_643727571 m1A Human chr18 + 36187579 36187579 36187579 GCGCGGCGGCGGAGTCAGGGCGGGAGCTGTGGACCTTCGCGGGTTCCCGGGACCCGAGCGCACCG GCGCGGCGGCGGAGTCAGGGCGGGAGCTGTGGTCCTTCGCGGGTTCCCGGGACCCGAGCGCACCG A T MOCOS Ensembl:ENSG00000075643 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:36187518..36187659 26863196 MeRIP-seq:(Medium) rs779808561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494200,Human_RBP_ID_5369378 64463 RMVar_ID_64463 Human_SNP_ID_643735219 m1A Human chr18 + 36215953 36215953 36215953 CCACATGTTGTCACTAACCTTTATCTCTATCCAATCAAATCCTGTGCTGCATTTGAGGTAAGGAA CCACATGTTGTCACTAACCTTTATCTCTATCCCATCAAATCCTGTGCTGCATTTGAGGTAAGGAA A C MOCOS Ensembl:ENSG00000075643 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:36215903..36251242 32194978 MeRIP-seq:(Medium) rs780546274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17909252,Human_RBP_ID_27462459 Human_Splice_Rec_1906181 RMVar_hsa_circ_58329,RMVar_hsa_circ_292029,RMVar_hsa_circ_327533,RMVar_hsa_circ_63813,RMVar_hsa_circ_24538,RMVar_hsa_circ_111241,RMVar_hsa_circ_367124,RMVar_hsa_circ_189675,RMVar_hsa_circ_297461,RMVar_hsa_circ_299572,RMVar_hsa_circ_347008,RMVar_hsa_circ_374603,RMVar_hsa_circ_344156,RMVar_hsa_circ_189677,RMVar_hsa_circ_189681,RMVar_hsa_circ_79014,RMVar_hsa_circ_189679,RMVar_hsa_circ_189680,RMVar_hsa_circ_189678,RMVar_hsa_circ_189676,RMVar_hsa_circ_347112,RMVar_hsa_circ_35425,RMVar_hsa_circ_189686,RMVar_hsa_circ_104160,RMVar_hsa_circ_297518,RMVar_hsa_circ_119952,RMVar_hsa_circ_189687,RMVar_hsa_circ_189688,RMVar_hsa_circ_335515 64464 RMVar_ID_64464 Human_SNP_ID_643826371 m1A Human chr18 + 36592432 36592432 36592432 CATGGATGAACTCTGCTGTGTGAAAAACGCTCACACAACTGTAGAGCTTAGCATGTGAAGTGCAC CATGGATGAACTCTGCTGTGTGAAAAACGCTCCCACAACTGTAGAGCTTAGCATGTGAAGTGCAC A C FHOD3 Ensembl:ENSG00000134775 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:36592422..36592535 26863196 MeRIP-seq:(Medium) rs1212094084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50640,RMVar_hsa_circ_24915,RMVar_hsa_circ_8058,RMVar_hsa_circ_27541,RMVar_hsa_circ_46964,RMVar_hsa_circ_287669,RMVar_hsa_circ_5900,RMVar_hsa_circ_77462,RMVar_hsa_circ_123027,RMVar_hsa_circ_281548,RMVar_hsa_circ_325166,RMVar_hsa_circ_189696,RMVar_hsa_circ_283677,RMVar_hsa_circ_274751,RMVar_hsa_circ_189698,RMVar_hsa_circ_189700,RMVar_hsa_circ_34334,RMVar_hsa_circ_189699,RMVar_hsa_circ_189697 64465 RMVar_ID_64465 Human_SNP_ID_643875832 m1A Human chr18 + 36796732 36796732 36796732 GAAAGAGGCCTACGGTCCACACGCAAAACTGGAGGTCACCCCTAGGGCCATCTGTGCATGGAAAC GAAAGAGGCCTACGGTCCACACGCAAAACTGGGGGTCACCCCTAGGGCCATCTGTGCATGGAAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:36796601..36796750 32194978 MeRIP-seq:(Medium) rs910271610 Functional Loss SNV dbSNP153 33..33 33 - - - 64466 RMVar_ID_64466 Human_SNP_ID_643875891 m1A Human chr18 - 36796890 36796890 36796890 AAAGAAAGGGCCTGTGCAGCCTGCAGGTGGCCAGAAAGGGCCCTCAGGACCCTCCGGTCCCTCCA AAAGAAAGGGCCTGTGCAGCCTGCAGGTGGCCGGAAAGGGCCCTCAGGACCCTCCGGTCCCTCCA T C TPGS2 Ensembl:ENSG00000134779 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:36796839..36796957 26863196 MeRIP-seq:(Medium) rs1339849950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508433,Human_RBP_ID_23769009,Human_RBP_ID_26979238 Human_miRNA_ID_2675990,Human_miRNA_ID_2926740 RMVar_hsa_circ_87694,RMVar_hsa_circ_123554,RMVar_hsa_circ_106713,RMVar_hsa_circ_116605,RMVar_hsa_circ_99248,RMVar_hsa_circ_189712,RMVar_hsa_circ_189714,RMVar_hsa_circ_189716,RMVar_hsa_circ_82335,RMVar_hsa_circ_189715,RMVar_hsa_circ_189713,RMVar_hsa_circ_189711 64467 RMVar_ID_64467 Human_SNP_ID_643883168 m1A Human chr18 + 36828878 36828878 36828878 GCATGCCGGGAACGGTAGTTCTCGGCGCCTGAAAGCGCGGCGCAGTGATGATGGGGGCCCGGGGT GCATGCCGGGAACGGTAGTTCTCGGCGCCTGAGAGCGCGGCGCAGTGATGATGGGGGCCCGGGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:36828835..36828994 26863196 MeRIP-seq:(Medium) rs1421523094 Functional Loss SNV dbSNP153 33..33 33 - - - 64468 RMVar_ID_64468 Human_SNP_ID_643883212 m1A Human chr18 - 36828963 36828963 36828963 GGAAGCTACGTCCCGGAGGTGCGGTGTGGGGCACCGGGCGGGGCCGCGGGAACCGGCGCCCCACG GGAAGCTACGTCCCGGAGGTGCGGTGTGGGGCGCCGGGCGGGGCCGCGGGAACCGGCGCCCCACG T C TPGS2 Ensembl:ENSG00000134779 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:36828912..36829001 26863196 MeRIP-seq:(Medium) rs561810746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508471,Human_RBP_ID_4494003,Human_RBP_ID_5319602,Human_RBP_ID_9327755,Human_RBP_ID_18420790 RMVar_hsa_circ_87694,RMVar_hsa_circ_189716,RMVar_hsa_circ_269111 64469 RMVar_ID_64469 Human_SNP_ID_644041282 m1A Human chr18 - 37485784 37485784 37485784 TAGAAAAGCAAAGGGAGGTACGAGAGGCAGACAGCCGGGAACACCGAGAGGCAGAGAAGCTCCGA TAGAAAAGCAAAGGGAGGTACGAGAGGCAGACGGCCGGGAACACCGAGAGGCAGAGAAGCTCCGA T C CELF4 Ensembl:ENSG00000101489 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:37485690..37485799 26863196 MeRIP-seq:(Medium) rs1240242608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1907055,Human_Splice_Rec_1907067 64470 RMVar_ID_64470 Human_SNP_ID_644563837 m1A Human chr18 - 39644541 39644541 39644541 AAGGAGAAGGAGGAGGAAGCAGAGGAGGAGGAAGAAGAGGAGAAATTACCAATATCTGAAAAGAG AAGGAGAAGGAGGAGGAAGCAGAGGAGGAGGAGGAAGAGGAGAAATTACCAATATCTGAAAAGAG T C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39644533..39644706 26863196 MeRIP-seq:(Medium) rs1176951404 Functional Loss SNV dbSNP153 33..33 33 - - - 64471 RMVar_ID_64471 Human_SNP_ID_644564886 m1A Human chr18 - 39648805 39648786 39648805 AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAG___________________GAAGGAAGGAAAGA CCTTTCTTTCTTTCTCTTTT C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39648673..39648927 26863196 MeRIP-seq:(Medium) rs1568105287 Functional Loss DEL dbSNP153 33..51 33 - - - 64472 RMVar_ID_64472 Human_SNP_ID_644564892 m1A Human chr18 - 39648805 39648791 39648805 AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAG______________GAAAGGAAGGAAGGAAAGA CTTTCTTTCTCTTTT C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39648673..39648927 26863196 MeRIP-seq:(Medium) rs1376405915 Functional Loss DEL dbSNP153 33..46 33 - - - 64473 RMVar_ID_64473 Human_SNP_ID_644564895 m1A Human chr18 - 39648797 39648795 39648797 AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGA__GAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA CTT C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:39648743..39648903 26863196 MeRIP-seq:(Medium) rs1159297919 Functional Loss DEL dbSNP153 33..34 33 - - - 64474 RMVar_ID_64474 Human_SNP_ID_644564899 m1A Human chr18 - 39648797 39648797 39648797 AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAGAGAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA T C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:39648743..39648903 26863196 MeRIP-seq:(Medium) rs202061211 Functional Loss SNV dbSNP153 33..33 33 - - - 64475 RMVar_ID_64475 Human_SNP_ID_644564900 m1A Human chr18 - 39648797 39648797 39648797 AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA AGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGACAGAAAGAAAGGAAGGAAGGAAAGAAGGAAGGA T G MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:39648743..39648903 26863196 MeRIP-seq:(Medium) rs202061211 Functional Loss SNV dbSNP153 33..33 33 - - - 64476 RMVar_ID_64476 Human_SNP_ID_644564901 m1A Human chr18 - 39648805 39648798 39648806 AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAA________AAAGAAAGAAAGGAAGGAAGGAAAGA TCTCTTTTC T MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39648673..39648927 26863196 MeRIP-seq:(Medium) rs1452956116 Functional Loss DEL dbSNP153 32..39 33 - - - 64477 RMVar_ID_64477 Human_SNP_ID_644564903 m1A Human chr18 - 39648805 39648802 39648806 AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAA____AGAGAAAGAAAGAAAGGAAGGAAGGAAAGA TTTTC T MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39648673..39648927 26863196 MeRIP-seq:(Medium) rs564626775 Functional Loss DEL dbSNP153 32..35 33 - - - 64478 RMVar_ID_64478 Human_SNP_ID_644564906 m1A Human chr18 - 39648805 39648803 39648806 AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAAGAAAAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA AAAGAAAGAGAAAGAAAGAAAGAGAAAGAAA___AAGAGAAAGAAAGAAAGGAAGGAAGGAAAGA TTTC T MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39648673..39648927 26863196 MeRIP-seq:(Medium) rs1475376437 Functional Loss DEL dbSNP153 32..34 33 - - - 64479 RMVar_ID_64479 Human_SNP_ID_644593662 m1A Human chr18 + 39771111 39771111 39771111 TTAACCACCTCTATTCCTTCCTCTCCAAATACAAGTGTTCAGTGCTAGTGCCTACCTTTGTGGTC TTAACCACCTCTATTCCTTCCTCTCCAAATACGAGTGTTCAGTGCTAGTGCCTACCTTTGTGGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39771101..39771209 26863196 MeRIP-seq:(Medium) rs1450170757 Functional Loss SNV dbSNP153 33..33 33 - - - 64480 RMVar_ID_64480 Human_SNP_ID_644600323 m1A Human chr18 + 39800232 39800232 39800232 GGCAGGGTTTTATTGGGTAAAAAGGGGAAAAAAGGGGGGACACAGGTATTCCCTCACAAGGTCAG GGCAGGGTTTTATTGGGTAAAAAGGGGAAAAAGGGGGGGACACAGGTATTCCCTCACAAGGTCAG A G lnc-PIK3C3-11 RNACentral:URS00008B795F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:39800186..39800260 26863196 MeRIP-seq:(Medium) rs1568141390 Functional Loss SNV dbSNP153 33..33 33 - - - 64481 RMVar_ID_64481 Human_SNP_ID_645155033 m1A Human chr18 - 41955316 41955316 41955316 GACGTTGATATCCAGGTCACAACTATAGATGTAGTGAAACTTCTCTGCTTCCCCCATCGCACCGT GACGTTGATATCCAGGTCACAACTATAGATGTGGTGAAACTTCTCTGCTTCCCCCATCGCACCGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:41955270..41955554 26863196 MeRIP-seq:(Medium) rs1284280087 Functional Loss SNV dbSNP153 33..33 33 - - - 64482 RMVar_ID_64482 Human_SNP_ID_645848850 m1A Human chr18 + 44679396 44679370 44679397 ACTGGCTGCGCCTCCCCCGGCTCTGGTCTGGGAAGCGGCTCTGGGCCCTCCGGGCGAGCAGCTTG ACTGGCT___________________________GCGGCTCTGGGCCCTCCGGGCGAGCAGCTTG TGCGCCTCCCCCGGCTCTGGTCTGGGAA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:44679351..44679484 26863196 MeRIP-seq:(Medium) rs1179369705 Functional Loss DEL dbSNP153 8..34 33 - - - 64483 RMVar_ID_64483 Human_SNP_ID_645848870 m1A Human chr18 - 44679444 44679444 44679444 GGTACCGACCGTCACCCCGCGATCTTCCTCGCAGGGGGCGCCGGCGCCCAAGCTGCTCGCCCGGA GGTACCGACCGTCACCCCGCGATCTTCCTCGCTGGGGGCGCCGGCGCCCAAGCTGCTCGCCCGGA T A AC120049.1 Ensembl:ENSG00000267414 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:44679394..44679482 26863196 MeRIP-seq:(Medium) rs1420044125 Functional Loss SNV dbSNP153 33..33 33 - - - 64484 RMVar_ID_64484 Human_SNP_ID_645849256 m1A Human chr18 - 44680214 44680214 44680214 CTCGGGGGGCGCCGGGGCCCCCGGGCGCGCGGAGGCGGCGGCGAGCGGCGGGCGCCCCGGCCGGC CTCGGGGGGCGCCGGGGCCCCCGGGCGCGCGGGGGCGGCGGCGAGCGGCGGGCGCCCCGGCCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:44680171..44680293 26863196 MeRIP-seq:(Medium) rs953776317 Functional Loss SNV dbSNP153 33..33 33 - - - 64485 RMVar_ID_64485 Human_SNP_ID_645849311 m1A Human chr18 + 44680392 44680392 44680392 GCCGGGGCCAGCGGAGCCGGAGCCGCCGGGACATGGGTGAGCACGCGCGGCGACCTTGGCCCGGG GCCGGGGCCAGCGGAGCCGGAGCCGCCGGGACGTGGGTGAGCACGCGCGGCGACCTTGGCCCGGG A G SETBP1 Ensembl:ENSG00000152217 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:44680341..44680440 26863196 MeRIP-seq:(Medium) rs1418710083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1908465 64486 RMVar_ID_64486 Human_SNP_ID_645849359 m1A Human chr18 + 44680558 44680558 44680558 GGTCTTTGACTTTGCACCCGGCGGGAAGGGGGAGACCGGGCCGAGGGGGCGGGATGCCGGTCCGG GGTCTTTGACTTTGCACCCGGCGGGAAGGGGGGGACCGGGCCGAGGGGGCGGGATGCCGGTCCGG A G SETBP1 Ensembl:ENSG00000152217 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:44680554..44680677 26863196 MeRIP-seq:(Medium) rs1325932190 Functional Loss SNV dbSNP153 33..33 33 - - - 64487 RMVar_ID_64487 Human_SNP_ID_645849461 m1A Human chr18 - 44680807 44680807 44680807 TCCCCCTCCCGAGTCCACTCCACCAACGCCAAACCCGCCAGCCCCGCCAGCCGGCTGCAGGACCG TCCCCCTCCCGAGTCCACTCCACCAACGCCAACCCCGCCAGCCCCGCCAGCCGGCTGCAGGACCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:44680679..44680806 26863196 MeRIP-seq:(Medium) rs943738575 Functional Loss SNV dbSNP153 33..33 33 - - - 64488 RMVar_ID_64488 Human_SNP_ID_645853971 m1A Human chr18 + 44701502 44701502 44701502 CCAGGACCTGGGAAGGGGATCCCGGTGGGCGGAGAGCGCATGGAGCCAGAGGAGGAGGATGAACT CCAGGACCTGGGAAGGGGATCCCGGTGGGCGGGGAGCGCATGGAGCCAGAGGAGGAGGATGAACT A G SETBP1 Ensembl:ENSG00000152217 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:44701414..44701678 26863196 MeRIP-seq:(Medium) rs767439164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101566,RMVar_hsa_circ_189806,RMVar_hsa_circ_189811,RMVar_hsa_circ_189815,RMVar_hsa_circ_85358,RMVar_hsa_circ_270537,RMVar_hsa_circ_330700,RMVar_hsa_circ_281656,RMVar_hsa_circ_106122,RMVar_hsa_circ_189817,RMVar_hsa_circ_84109,RMVar_hsa_circ_189816,RMVar_hsa_circ_189813,RMVar_hsa_circ_189814,RMVar_hsa_circ_189812,RMVar_hsa_circ_189809,RMVar_hsa_circ_189810,RMVar_hsa_circ_189808 64489 RMVar_ID_64489 Human_SNP_ID_645853985 m1A Human chr18 + 44701541 44701541 44701541 ATGGAGCCAGAGGAGGAGGATGAACTAGGCTCAGGGCGGGATGTGGATTCCAACTCCAACGCGGA ATGGAGCCAGAGGAGGAGGATGAACTAGGCTCCGGGCGGGATGTGGATTCCAACTCCAACGCGGA A C SETBP1 Ensembl:ENSG00000152217 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:44701492..44701658;chr18:44701495..44701638 26863196 MeRIP-seq:(Medium) rs982350261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526587,Human_RBP_ID_6687233,Human_RBP_ID_8827277 RMVar_hsa_circ_101566,RMVar_hsa_circ_189806,RMVar_hsa_circ_189811,RMVar_hsa_circ_189815,RMVar_hsa_circ_85358,RMVar_hsa_circ_270537,RMVar_hsa_circ_330700,RMVar_hsa_circ_281656,RMVar_hsa_circ_106122,RMVar_hsa_circ_189817,RMVar_hsa_circ_84109,RMVar_hsa_circ_189816,RMVar_hsa_circ_189813,RMVar_hsa_circ_189814,RMVar_hsa_circ_189812,RMVar_hsa_circ_189809,RMVar_hsa_circ_189810,RMVar_hsa_circ_189808 64490 RMVar_ID_64490 Human_SNP_ID_645865611 m1A Human chr18 - 44751020 44751020 44751020 ATGACCCCCAAATACCAGGCTGACCCTTGTGCACTTAAGTTTGCTCATACTGCTTCCCACTCCAT ATGACCCCCAAATACCAGGCTGACCCTTGTGCCCTTAAGTTTGCTCATACTGCTTCCCACTCCAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:44750943..44751052 26863196 MeRIP-seq:(Medium) rs1424323314 Functional Loss SNV dbSNP153 33..33 33 - - - 64491 RMVar_ID_64491 Human_SNP_ID_645866211 m1A Human chr18 + 44753778 44753777 44753778 CTAAAGGTGGTGTGTGGTGGACCAGTGACAGCAGGGTGAGGGAGGAAGGAAAAAGACTGAATCAT CTAAAGGTGGTGTGTGGTGGACCAGTGACAGC_GGGTGAGGGAGGAAGGAAAAAGACTGAATCAT CA C SETBP1 Ensembl:ENSG00000152217 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:44753763..44753828 26863196 MeRIP-seq:(Medium) rs1043178365 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_101566,RMVar_hsa_circ_189806,RMVar_hsa_circ_189811,RMVar_hsa_circ_85358,RMVar_hsa_circ_330700,RMVar_hsa_circ_281656,RMVar_hsa_circ_189812,RMVar_hsa_circ_189809,RMVar_hsa_circ_189810,RMVar_hsa_circ_189808 64492 RMVar_ID_64492 Human_SNP_ID_645914500 m1A Human chr18 + 44953188 44953188 44953188 CACGAGATCAGAGAACCTGGACGTGTTCAGTGAAATGAACCCTTCGAATGACAAGTGGGACAGTG CACGAGATCAGAGAACCTGGACGTGTTCAGTGCAATGAACCCTTCGAATGACAAGTGGGACAGTG A C SETBP1 Ensembl:ENSG00000152217 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:44953138..44953242 26863196 MeRIP-seq:(Medium) rs1256820736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101566,RMVar_hsa_circ_189806,RMVar_hsa_circ_85358,RMVar_hsa_circ_330700,RMVar_hsa_circ_189808,RMVar_hsa_circ_189826,RMVar_hsa_circ_364353,RMVar_hsa_circ_270781 64493 RMVar_ID_64493 Human_SNP_ID_383835957 m1A Human chr8 - 135557566 135557566 135557566 TTTACACCTACCTGGTTATTGCTGGGGCTGGTACACCTCTTGTACGCAAGGTGGGTTTCCCTCGA TTTACACCTACCTGGTTATTGCTGGGGCTGGTGCACCTCTTGTACGCAAGGTGGGTTTCCCTCGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:135557448..135581889 32194978 MeRIP-seq:(Medium) rs1466208339 Functional Loss SNV dbSNP153 33..33 33 - - - 64494 RMVar_ID_64494 Human_SNP_ID_384101293 m1A Human chr8 + 136589631 136589631 136589631 AAAGAAATAAGTAAGGAGAGGAGAGGAAAGGAAAGGAGAGAAAGGAGAGGGGAGGAGAAGAGAGA AAAGAAATAAGTAAGGAGAGGAGAGGAAAGGAGAGGAGAGAAAGGAGAGGGGAGGAGAAGAGAGA A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:136589598..136589774 26863196 MeRIP-seq:(Medium) rs1441717748 Functional Loss SNV dbSNP153 33..33 33 - - - 64495 RMVar_ID_64495 Human_SNP_ID_384102070 m1A Human chr8 + 136593045 136593045 136593045 TTTTCCAAGTTAGACACAGAAAGGTGGAAAAGAACATAGCAGGCTGAAGATAGGATGCTCACAGG TTTTCCAAGTTAGACACAGAAAGGTGGAAAAGTACATAGCAGGCTGAAGATAGGATGCTCACAGG A T LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:136593040..136593144 26863196 MeRIP-seq:(Medium) rs1266618039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8681729 64496 RMVar_ID_64496 Human_SNP_ID_384918517 m1A Human chr8 + 139730557 139730557 139730557 CCTACGGCACCATCTCTCCTGCCAAGTTGCCCATGGGGGTCTCCAGGAAGAAAACCAGCCTTGGG CCTACGGCACCATCTCTCCTGCCAAGTTGCCCGTGGGGGTCTCCAGGAAGAAAACCAGCCTTGGG A G HSALNG0068987 RNACentral:URS0000EAB47F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:139730512..139730660 26863196 MeRIP-seq:(Medium) rs1205207296 Functional Loss SNV dbSNP153 33..33 33 - - - 64497 RMVar_ID_64497 Human_SNP_ID_384924429 m1A Human chr8 + 139751765 139751765 139751765 CCATCCATCCATCCATCCATCCTCCAGCAGACAAGAGATGCCCTCAGGCTGCTGCCCCTTTGATT CCATCCATCCATCCATCCATCCTCCAGCAGACCAGAGATGCCCTCAGGCTGCTGCCCCTTTGATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:139751715..139751841 26863196 MeRIP-seq:(Medium) rs930075139 Functional Loss SNV dbSNP153 33..33 33 - - - 64498 RMVar_ID_64498 Human_SNP_ID_384924546 m1A Human chr8 + 139752158 139752158 139752158 CATCCATCTATATATCGATCCATCTATATACCATCCATCCACTACCATCTATCCGCCATCCATCC CATCCATCTATATATCGATCCATCTATATACCGTCCATCCACTACCATCTATCCGCCATCCATCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:139752145..139752349 26863196 MeRIP-seq:(Medium) rs1438782567 Functional Loss SNV dbSNP153 33..33 33 - - - 64499 RMVar_ID_64499 Human_SNP_ID_384924693 m1A Human chr8 - 139752628 139752628 139752628 GAATGGTGGATTTTGGATGGATGGATAGATGGATGGTAGATGGACAGTAGATGGATGTGTGAATG GAATGGTGGATTTTGGATGGATGGATAGATGGTTGGTAGATGGACAGTAGATGGATGTGTGAATG T A TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:139751695..139753029 26863196 MeRIP-seq:(Medium) rs1431853480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24247663 64500 RMVar_ID_64500 Human_SNP_ID_384937652 m1A Human chr8 + 139800901 139800884 139800902 TCCCTCCCTCTGGTATCTTCCCGCCCTCCGGTACCTTCCCTCCCTCCGGTACCTTCCCTCCCTCC TCCCTCCCTCTGGTAT__________________CTTCCCTCCCTCCGGTACCTTCCCTCCCTCC TCTTCCCGCCCTCCGGTAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:139800896..139801040 26863196 MeRIP-seq:(Medium) rs1349379458 Functional Loss DEL dbSNP153 17..34 33 - - - 64501 RMVar_ID_64501 Human_SNP_ID_384938994 m1A Human chr8 + 139804786 139804786 139804786 GCCACCACTACCCACCACCACCACCAAGCACCACCGCCGCAGCCACCACCCACCACCAAGGCAGC GCCACCACTACCCACCACCACCACCAAGCACCGCCGCCGCAGCCACCACCCACCACCAAGGCAGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:139804770..139804867 26863196 MeRIP-seq:(Medium) rs1207674303 Functional Loss SNV dbSNP153 33..33 33 - - - 64502 RMVar_ID_64502 Human_SNP_ID_384940194 m1A Human chr8 - 139809631 139809631 139809631 AGGGAGAGCAGGAAGATCAGGGCTGGGCTGTCAGGAGGCCAGGCTCTGGAGGACCCCAGATGCCA AGGGAGAGCAGGAAGATCAGGGCTGGGCTGTCGGGAGGCCAGGCTCTGGAGGACCCCAGATGCCA T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:139809608..139809755 26863196 MeRIP-seq:(Medium) rs1162661886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5224002 64503 RMVar_ID_64503 Human_SNP_ID_384952650 m1A Human chr8 - 139857239 139857239 139857239 GACTCCTGCGTGTGTCCTGCGATACCAGGCCCATGAGCCGCCGCCAGCCTCTGGCCTCACCTCCT GACTCCTGCGTGTGTCCTGCGATACCAGGCCCGTGAGCCGCCGCCAGCCTCTGGCCTCACCTCCT T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:139857131..139857274 26863196 MeRIP-seq:(Medium) rs1159311551 Functional Loss SNV dbSNP153 33..33 33 - - - 64504 RMVar_ID_64504 Human_SNP_ID_384956365 m1A Human chr8 - 139872126 139872122 139872126 CATCCAACCATTTACCCACCAGCCCATCCACCAGCCCACCCATCCATCCATCCATCCATCCACTC CATCCAACCATTTACCCACCAGCCCATCCACC____CACCCATCCATCCATCCATCCATCCACTC GGGCT G TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:139871900..139872172 26863196 MeRIP-seq:(Medium) rs1347162487 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_217650,Human_RBP_ID_24537222 64505 RMVar_ID_64505 Human_SNP_ID_384958491 m1A Human chr8 + 139879479 139879479 139879479 CCGTGGCTGGCTAACTAAGGTCTGAACTCTCCACCTGTCCCTGCCCAGATGGTAAACTCAACCCA CCGTGGCTGGCTAACTAAGGTCTGAACTCTCCGCCTGTCCCTGCCCAGATGGTAAACTCAACCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:139879452..139879566 26863196 MeRIP-seq:(Medium) rs1256434591 Functional Loss SNV dbSNP153 33..33 33 - - - 64506 RMVar_ID_64506 Human_SNP_ID_385017718 m1A Human chr8 - 140105594 140105594 140105594 TAAGAGAAGCATAGATGGAGCTCATTCCAGAAAGGTCCACAGGGTGCTCAAAGGGAGGGAAGCGT TAAGAGAAGCATAGATGGAGCTCATTCCAGAATGGTCCACAGGGTGCTCAAAGGGAGGGAAGCGT T A TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140105592..140105738 26863196 MeRIP-seq:(Medium) rs1336046503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 64507 RMVar_ID_64507 Human_SNP_ID_385021482 m1A Human chr8 - 140120505 140120505 140120505 GAATGGTTGTTGGATGGATAGATGGAGGCTAGATGGATGAGAGTATTGCAGAAAAGCTGTATGGA GAATGGTTGTTGGATGGATAGATGGAGGCTAGGTGGATGAGAGTATTGCAGAAAAGCTGTATGGA T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140120500..140120949 26863196 MeRIP-seq:(Medium) rs933200082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5658139,Human_RBP_ID_17319903,Human_RBP_ID_24247822 RMVar_hsa_circ_71575 64508 RMVar_ID_64508 Human_SNP_ID_385021537 m1A Human chr8 + 140120636 140120636 140120636 TCCAACATCCATCCATCCGTCCAACATCCAACATCCATCCATCCATCCATTCATCCATCCACCCA TCCAACATCCATCCATCCGTCCAACATCCAACGTCCATCCATCCATCCATTCATCCATCCACCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140120614..140120800 26863196 MeRIP-seq:(Medium) rs1002913331 Functional Loss SNV dbSNP153 33..33 33 - - - 64509 RMVar_ID_64509 Human_SNP_ID_385022331 m1A Human chr8 - 140123534 140123533 140123534 GGGGCTCGTGGCTGGAGAGGAAGCAGTATGTCAGTACCCCAGATGCCCATGGCAGAGTGGGTGTG GGGGCTCGTGGCTGGAGAGGAAGCAGTATGTC_GTACCCCAGATGCCCATGGCAGAGTGGGTGTG CT C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140123528..140123593 26863196 MeRIP-seq:(Medium) rs762956437 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 64510 RMVar_ID_64510 Human_SNP_ID_385032749 m1A Human chr8 + 140164787 140164787 140164787 CACACAAGTCAGGAACCAAAATCCACCCCGCCATGTCCTGCCAATCCCTGATGTGTGTCCATTTT CACACAAGTCAGGAACCAAAATCCACCCCGCCCTGTCCTGCCAATCCCTGATGTGTGTCCATTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140164781..140164875 26863196 MeRIP-seq:(Medium) rs1256619335 Functional Loss SNV dbSNP153 33..33 33 - - - 64511 RMVar_ID_64511 Human_SNP_ID_385042966 m1A Human chr8 - 140205844 140205842 140205844 CAGTAATACTGTGTGGGAATCAGCATCTGGAGAGTGAGGTGAAAGGACAAGAATGGTTGCATGGT CAGTAATACTGTGTGGGAATCAGCATCTGGAG__TGAGGTGAAAGGACAAGAATGGTTGCATGGT ACT A TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:140205842..140205945 26863196 MeRIP-seq:(Medium) rs1479416204 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16369872 RMVar_hsa_circ_71575 64512 RMVar_ID_64512 Human_SNP_ID_385121263 m1A Human chr8 + 140508015 140508015 140508015 AATGACTGCAAACATCACCTGCCAATTCTACAAGCTGAGCTTCTCATCCCTATTCTCTCTCCTTT AATGACTGCAAACATCACCTGCCAATTCTACAGGCTGAGCTTCTCATCCCTATTCTCTCTCCTTT A G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140507965..140508056 26863196 MeRIP-seq:(Medium) rs985982907 Functional Loss SNV dbSNP153 33..33 33 - - - 64513 RMVar_ID_64513 Human_SNP_ID_385121606 m1A Human chr8 - 140509250 140509250 140509250 CTGACGAGGAAAATGCCTGGGCAGTTTGAGGAACTGAAAAGCCAGTGTGTCTGGAGCTTAGTGAG CTGACGAGGAAAATGCCTGGGCAGTTTGAGGACCTGAAAAGCCAGTGTGTCTGGAGCTTAGTGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140509199..140509390 26863196 MeRIP-seq:(Medium) rs1200637015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16370107 64514 RMVar_ID_64514 Human_SNP_ID_385121695 m1A Human chr8 - 140509493 140509491 140509493 GCGCCACTGCACTCCAGCAGCCTGGGCGACAGAGGGAGACTCCATCTCAAAAAAAAAAAAAAAAA GCGCCACTGCACTCCAGCAGCCTGGGCGACAG__GGAGACTCCATCTCAAAAAAAAAAAAAAAAA CCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:140509443..140509531 26863196 MeRIP-seq:(Medium) rs1279796448 Functional Loss DEL dbSNP153 33..34 33 - - - 64515 RMVar_ID_64515 Human_SNP_ID_385122020 m1A Human chr8 - 140510516 140510516 140510516 ACCAAGGGGACAGCAGCTGGGAGGAGAGAGGCAGGAGATGGTCAGGGGCCAGACCAGGGAAGGCC ACCAAGGGGACAGCAGCTGGGAGGAGAGAGGCCGGAGATGGTCAGGGGCCAGACCAGGGAAGGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140510465..140510950 26863196 MeRIP-seq:(Medium) rs904736493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070364 64516 RMVar_ID_64516 Human_SNP_ID_385122367 m1A Human chr8 + 140511402 140511402 140511402 CTCGCCTCCCCACACTACAACTCCCACGGGGCAGCGGGCGCGGCTCCCCGTACCCACCAGCTGGC CTCGCCTCCCCACACTACAACTCCCACGGGGCGGCGGGCGCGGCTCCCCGTACCCACCAGCTGGC A G CHRAC1 Ensembl:ENSG00000104472 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140511359..140511549 26863196 MeRIP-seq:(Medium) rs766183606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995742,Human_RBP_ID_5514466,Human_RBP_ID_26832428 64517 RMVar_ID_64517 Human_SNP_ID_385123786 m1A Human chr8 + 140515422 140515422 140515422 TTCCAGGCCGAGATTGAGCACCTCATGTACCTACGCCACAGACAGCCAGAGGGAAAGCGACCCAG TTCCAGGCCGAGATTGAGCACCTCATGTACCTGCGCCACAGACAGCCAGAGGGAAAGCGACCCAG A G CHRAC1 Ensembl:ENSG00000104472 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:140515166..140515659 32194978 MeRIP-seq:(Medium) rs753347508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1054516,Human_RBP_ID_16370200,Human_RBP_ID_17319907,Human_RBP_ID_17434060,Human_RBP_ID_17544623 Human_miRNA_ID_2331475,Human_miRNA_ID_2964558 RMVar_hsa_circ_111855,RMVar_hsa_circ_254669 64518 RMVar_ID_64518 Human_SNP_ID_385129879 m1A Human chr8 + 140538618 140538618 140538618 ACGCCGCCACCTCTCCTCCCCTCCTCAGCACCACCTTCCAGCCCTGCCACAGGGACCTGCCGGGA ACGCCGCCACCTCTCCTCCCCTCCTCAGCACCCCCTTCCAGCCCTGCCACAGGGACCTGCCGGGA A C RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140538575..140538674 26863196 MeRIP-seq:(Medium) rs918821799 Functional Loss SNV dbSNP153 33..33 33 - - - 64519 RMVar_ID_64519 Human_SNP_ID_385131703 m1A Human chr8 - 140545129 140545115 140545129 GGATGTGGGCGGAGAGTGAGTCACAGGCATGCAGGGAAATGGATGCGGGGAGAGGGCAGCAGAGG GGATGTGGGCGGAGAGTGAGTCACAGGCATGC______________GGGGAGAGGGCAGCAGAGG CGCATCCATTTCCCT C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140545126..140545263 26863196 MeRIP-seq:(Medium) rs757693776 Functional Loss DEL dbSNP153 33..46 33 - - - RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_10339,RMVar_hsa_circ_343080,RMVar_hsa_circ_254673,RMVar_hsa_circ_269128,RMVar_hsa_circ_358666,RMVar_hsa_circ_37102,RMVar_hsa_circ_298373,RMVar_hsa_circ_16504,RMVar_hsa_circ_254675,RMVar_hsa_circ_4690,RMVar_hsa_circ_301532,RMVar_hsa_circ_254676 64520 RMVar_ID_64520 Human_SNP_ID_385131706 m1A Human chr8 - 140545129 140545129 140545129 GGATGTGGGCGGAGAGTGAGTCACAGGCATGCAGGGAAATGGATGCGGGGAGAGGGCAGCAGAGG GGATGTGGGCGGAGAGTGAGTCACAGGCATGCGGGGAAATGGATGCGGGGAGAGGGCAGCAGAGG T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140545126..140545263 26863196 MeRIP-seq:(Medium) rs2944770 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7881 RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_10339,RMVar_hsa_circ_343080,RMVar_hsa_circ_254673,RMVar_hsa_circ_269128,RMVar_hsa_circ_358666,RMVar_hsa_circ_37102,RMVar_hsa_circ_298373,RMVar_hsa_circ_16504,RMVar_hsa_circ_254675,RMVar_hsa_circ_4690,RMVar_hsa_circ_301532,RMVar_hsa_circ_254676 64521 RMVar_ID_64521 Human_SNP_ID_385132828 m1A Human chr8 + 140549200 140549200 140549200 ACGTGTTCTTCAGGTGCCGGAACATGGGCTCCACGCTGTCCGCCCCCTGCGCGTATTTGCAGAAG ACGTGTTCTTCAGGTGCCGGAACATGGGCTCCGCGCTGTCCGCCCCCTGCGCGTATTTGCAGAAG A G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:140549126..140549200 32194978 MeRIP-seq:(Medium) rs1256947908 Functional Loss SNV dbSNP153 33..33 33 - - - 64522 RMVar_ID_64522 Human_SNP_ID_385142776 m1A Human chr8 - 140585277 140585277 140585277 CTTGCACCTCCTGCGCCGCCGCCCCCCATCCAAGGATATGCCTTCAAGCCTCCACCTAGACCCGA CTTGCACCTCCTGCGCCGCCGCCCCCCATCCAGGGATATGCCTTCAAGCCTCCACCTAGACCCGA T C AGO2 Ensembl:ENSG00000123908 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr8:140585229..140585346;chr8:140585226..140585377 26863196 MeRIP-seq:(Medium) rs372212871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3973353,Human_RBP_ID_4972147,Human_RBP_ID_9338382,Human_RBP_ID_17544713,Human_RBP_ID_22115179,Human_RBP_ID_27536131 Human_Splice_Rec_1015792,Human_Splice_Rec_1015826,Human_Splice_Rec_1015902,Human_Splice_Rec_1015908 Human_miRNA_ID_2490193,Human_miRNA_ID_2752275,Human_miRNA_ID_2931813 RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_254673,RMVar_hsa_circ_358666,RMVar_hsa_circ_254675,RMVar_hsa_circ_301532,RMVar_hsa_circ_374147,RMVar_hsa_circ_79763,RMVar_hsa_circ_254677,RMVar_hsa_circ_254680,RMVar_hsa_circ_329497,RMVar_hsa_circ_254681,RMVar_hsa_circ_343450,RMVar_hsa_circ_254685,RMVar_hsa_circ_254686,RMVar_hsa_circ_82751,RMVar_hsa_circ_370770,RMVar_hsa_circ_327307,RMVar_hsa_circ_254687,RMVar_hsa_circ_76427,RMVar_hsa_circ_254688,RMVar_hsa_circ_309313,RMVar_hsa_circ_254690,RMVar_hsa_circ_276809,RMVar_hsa_circ_254689,RMVar_hsa_circ_300236,RMVar_hsa_circ_254691,RMVar_hsa_circ_254692 64523 RMVar_ID_64523 Human_SNP_ID_385147361 m1A Human chr8 + 140601214 140601214 140601214 CGGCCACAAGGCACCCAATGCGCTCCTGCCCCAGGGCCTTTGCACTTCCTGTCTACTCTTTCCTC CGGCCACAAGGCACCCAATGCGCTCCTGCCCCCGGGCCTTTGCACTTCCTGTCTACTCTTTCCTC A C RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:140601210..140601384 26863196 MeRIP-seq:(Medium) rs1236287269 Functional Loss SNV dbSNP153 33..33 33 - - - 64524 RMVar_ID_64524 Human_SNP_ID_385149690 m1A Human chr8 - 140609532 140609532 140609532 GCAGATTCCTGAGGGAGTGAGGCCGCAGCTGTAGCAGAGGAAGAATTGATGACGAGGCCGGTGCG GCAGATTCCTGAGGGAGTGAGGCCGCAGCTGTGGCAGAGGAAGAATTGATGACGAGGCCGGTGCG T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140609529..140609620 26863196 MeRIP-seq:(Medium) rs991217892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267986,Human_RBP_ID_16371654 64525 RMVar_ID_64525 Human_SNP_ID_385149691 m1A Human chr8 - 140609532 140609532 140609532 GCAGATTCCTGAGGGAGTGAGGCCGCAGCTGTAGCAGAGGAAGAATTGATGACGAGGCCGGTGCG GCAGATTCCTGAGGGAGTGAGGCCGCAGCTGTCGCAGAGGAAGAATTGATGACGAGGCCGGTGCG T G AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140609529..140609620 26863196 MeRIP-seq:(Medium) rs991217892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267986,Human_RBP_ID_16371654 64526 RMVar_ID_64526 Human_SNP_ID_385153464 m1A Human chr8 - 140623653 140623653 140623653 GGCTGCATCCATAGCACTGATGGAGACAGGTAACAGGTGTGCACGGGAGGGAAGCATGGCCACAT GGCTGCATCCATAGCACTGATGGAGACAGGTAGCAGGTGTGCACGGGAGGGAAGCATGGCCACAT T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:140623651..140623736 26863196 MeRIP-seq:(Medium) rs376268859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267987,Human_RBP_ID_3886995,Human_RBP_ID_5328927,Human_RBP_ID_8154759,Human_RBP_ID_18466830,Human_RBP_ID_22747525,Human_RBP_ID_23251621,Human_RBP_ID_26795585 64527 RMVar_ID_64527 Human_SNP_ID_385153829 m1A Human chr8 + 140624962 140624962 140624962 CATCCCGCTCCTTCCAACGGCCCCCTTGCTCCAGAGCATGCCCTCCACTGGGACCATCCCAGCAG CATCCCGCTCCTTCCAACGGCCCCCTTGCTCCGGAGCATGCCCTCCACTGGGACCATCCCAGCAG A G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140624959..140625194 26863196 MeRIP-seq:(Medium) rs7823699 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7882,GWAS_ID_7883 64528 RMVar_ID_64528 Human_SNP_ID_385156339 m1A Human chr8 + 140634276 140634276 140634276 GCACAGAGCCAACAGCTCCAGCAGTGGGGGCCACCATCAACGGACCAAGGTGGGCCAGGGGGCCT GCACAGAGCCAACAGCTCCAGCAGTGGGGGCCGCCATCAACGGACCAAGGTGGGCCAGGGGGCCT A G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140634268..140634433 26863196 MeRIP-seq:(Medium) rs907774447 Functional Loss SNV dbSNP153 33..33 33 - - - 64529 RMVar_ID_64529 Human_SNP_ID_385156697 m1A Human chr8 + 140635378 140635356 140635379 CGGCTCGCCCGCCCCCGGCCCCCGCCGCCCCGACCCCGCGGCCCCCCGATCCCCGGCCCCTGCCG CGGCTCGCCCG_______________________CCCGCGGCCCCCCGATCCCCGGCCCCTGCCG GCCCCCGGCCCCCGCCGCCCCGAC G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr8:140635370..140635675;chr8:140635301..140635531 26863196 MeRIP-seq:(Medium) rs1223749797 Functional Loss DEL dbSNP153 12..34 33 - - - 64530 RMVar_ID_64530 Human_SNP_ID_385156704 m1A Human chr8 + 140635378 140635364 140635378 CGGCTCGCCCGCCCCCGGCCCCCGCCGCCCCGACCCCGCGGCCCCCCGATCCCCGGCCCCTGCCG CGGCTCGCCCGCCCCCGGC______________CCCCGCGGCCCCCCGATCCCCGGCCCCTGCCG CCCCCGCCGCCCCGA C RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr8:140635370..140635675;chr8:140635301..140635531 26863196 MeRIP-seq:(Medium) rs1317566649 Functional Loss DEL dbSNP153 20..33 33 - - - 64531 RMVar_ID_64531 Human_SNP_ID_385165265 m1A Human chr8 + 140668384 140668384 140668384 CATTCTCGTACACCTTATCATTCGACCGGTCCAGGTTGGCAGTAGGAGGGGGGCTGATTTCCTGG CATTCTCGTACACCTTATCATTCGACCGGTCCCGGTTGGCAGTAGGAGGGGGGCTGATTTCCTGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:140668333..140668469 26863196 MeRIP-seq:(Medium) rs1472886111 Functional Loss SNV dbSNP153 33..33 33 - - - 64532 RMVar_ID_64532 Human_SNP_ID_385172804 m1A Human chr8 - 140695152 140695152 140695152 TGGTGTCACCAAAAATAACATTGTGCTACCAAATGAAATAAAATTCAGAATGAGGAGTCCATGTC TGGTGTCACCAAAAATAACATTGTGCTACCAAGTGAAATAAAATTCAGAATGAGGAGTCCATGTC T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140695150..140695299 26863196 MeRIP-seq:(Medium) rs1170804069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84244,RMVar_hsa_circ_101087,RMVar_hsa_circ_254694,RMVar_hsa_circ_254695,RMVar_hsa_circ_372352,RMVar_hsa_circ_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,RMVar_hsa_circ_83150,RMVar_hsa_circ_254697,RMVar_hsa_circ_254699,RMVar_hsa_circ_254700,RMVar_hsa_circ_254698,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_7623,RMVar_hsa_circ_254702,RMVar_hsa_circ_71603,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_348448,RMVar_hsa_circ_22418,RMVar_hsa_circ_69895,RMVar_hsa_circ_10045,RMVar_hsa_circ_108356,RMVar_hsa_circ_24582,RMVar_hsa_circ_85561,RMVar_hsa_circ_297222,RMVar_hsa_circ_323686,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_305123,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_63939,RMVar_hsa_circ_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709 64533 RMVar_ID_64533 Human_SNP_ID_385187891 m1A Human chr8 + 140755434 140755434 140755434 CCCTTTGTTTCCTATCCCTCTACTCCGCGGCCACACCGTCCTCCTGGTGGTGTACTGTCCTGCCC CCCTTTGTTTCCTATCCCTCTACTCCGCGGCCTCACCGTCCTCCTGGTGGTGTACTGTCCTGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140755383..140755483 26863196 MeRIP-seq:(Medium) rs944427548 Functional Loss SNV dbSNP153 33..33 33 - - - 64534 RMVar_ID_64534 Human_SNP_ID_385210312 m1A Human chr8 - 140847804 140847804 140847804 GCTAGCAGGCTAGGAGGCAGTCATTGAAGAACAGGATGTTTGAAAATTTTTTTAGGGTAGAAGTC GCTAGCAGGCTAGGAGGCAGTCATTGAAGAACGGGATGTTTGAAAATTTTTTTAGGGTAGAAGTC T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140847802..140847952 26863196 MeRIP-seq:(Medium) rs532541999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_9428,RMVar_hsa_circ_6314,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_55128,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_14253,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_271231,RMVar_hsa_circ_335902,RMVar_hsa_circ_376365,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_363588,RMVar_hsa_circ_63759,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_254740,RMVar_hsa_circ_34776,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_286717,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_276971,RMVar_hsa_circ_254761,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_254767,RMVar_hsa_circ_254768,RMVar_hsa_circ_357556,RMVar_hsa_circ_302704,RMVar_hsa_circ_309613,RMVar_hsa_circ_282064,RMVar_hsa_circ_275014,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_93272,RMVar_hsa_circ_254795,RMVar_hsa_circ_254791,RMVar_hsa_circ_281046,RMVar_hsa_circ_254790,RMVar_hsa_circ_254789,RMVar_hsa_circ_349494,RMVar_hsa_circ_281217,RMVar_hsa_circ_64312,RMVar_hsa_circ_278228,RMVar_hsa_circ_254793,RMVar_hsa_circ_254794,RMVar_hsa_circ_254792,RMVar_hsa_circ_254799,RMVar_hsa_circ_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_364237,RMVar_hsa_circ_286215,RMVar_hsa_circ_274174,RMVar_hsa_circ_278354,RMVar_hsa_circ_254797,RMVar_hsa_circ_254798,RMVar_hsa_circ_254796,RMVar_hsa_circ_254801,RMVar_hsa_circ_280309,RMVar_hsa_circ_314660,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802 64535 RMVar_ID_64535 Human_SNP_ID_385220730 m1A Human chr8 - 140890768 140890768 140890768 TACACAAAAAATTATTTTGTTCTTTTAACAGAATATGACAGATACCTAGCATCTAGCAAAATAAT TACACAAAAAATTATTTTGTTCTTTTAACAGAGTATGACAGATACCTAGCATCTAGCAAAATAAT T C PTK2 Ensembl:ENSG00000169398 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:140890701..140890841 26863410 MeRIP-seq:(Medium) rs570437652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1015916,Human_Splice_Rec_1015978,Human_Splice_Rec_1016126,Human_Splice_Rec_1016188,Human_Splice_Rec_1016296,Human_Splice_Rec_1016358,Human_Splice_Rec_1016424,Human_Splice_Rec_1016782,Human_Splice_Rec_1016790,Human_Splice_Rec_1016802,Human_Splice_Rec_1016818,Human_Splice_Rec_1016826,Human_Splice_Rec_1016832,Human_Splice_Rec_1016840,Human_Splice_Rec_1016844,Human_Splice_Rec_1016850,Human_Splice_Rec_1016856,Human_Splice_Rec_1016862,Human_Splice_Rec_1016866,Human_Splice_Rec_1016872,Human_Splice_Rec_1016878 Human_miRNA_ID_2365231,Human_miRNA_ID_2365232,Human_miRNA_ID_2365233,Human_miRNA_ID_2365234,Human_miRNA_ID_2365235,Human_miRNA_ID_2365236 RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_6314,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_254709,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_293517,RMVar_hsa_circ_2596,RMVar_hsa_circ_14253,RMVar_hsa_circ_342408,RMVar_hsa_circ_271231,RMVar_hsa_circ_376365,RMVar_hsa_circ_298567,RMVar_hsa_circ_270177,RMVar_hsa_circ_254734,RMVar_hsa_circ_363588,RMVar_hsa_circ_63759,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_349698,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254758,RMVar_hsa_circ_332870,RMVar_hsa_circ_254767,RMVar_hsa_circ_357556,RMVar_hsa_circ_309613,RMVar_hsa_circ_282064,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_280042,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_93272,RMVar_hsa_circ_122662,RMVar_hsa_circ_254795,RMVar_hsa_circ_254789,RMVar_hsa_circ_349494,RMVar_hsa_circ_64312,RMVar_hsa_circ_278228,RMVar_hsa_circ_254793,RMVar_hsa_circ_254794,RMVar_hsa_circ_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_286215,RMVar_hsa_circ_254797,RMVar_hsa_circ_254796,RMVar_hsa_circ_270852,RMVar_hsa_circ_280309,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802,RMVar_hsa_circ_322669,RMVar_hsa_circ_274966,RMVar_hsa_circ_254806,RMVar_hsa_circ_254805,RMVar_hsa_circ_273424,RMVar_hsa_circ_254808,RMVar_hsa_circ_311931,RMVar_hsa_circ_270085,RMVar_hsa_circ_9006,RMVar_hsa_circ_254809,RMVar_hsa_circ_254810,RMVar_hsa_circ_254811,RMVar_hsa_circ_316559,RMVar_hsa_circ_334120,RMVar_hsa_circ_18344,RMVar_hsa_circ_254812 64536 RMVar_ID_64536 Human_SNP_ID_385240823 m1A Human chr8 + 140969604 140969604 140969604 ACACCATCTTCTCCTGGTTTTCTTCTTACCTCACAGGTGGTTTCTTTCCAGTCTCTACAGCTGTT ACACCATCTTCTCCTGGTTTTCTTCTTACCTCGCAGGTGGTTTCTTTCCAGTCTCTACAGCTGTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140969602..140969667 26863196 MeRIP-seq:(Medium) rs1026297960 Functional Loss SNV dbSNP153 33..33 33 - - - 64537 RMVar_ID_64537 Human_SNP_ID_385249119 m1A Human chr8 - 141001197 141001197 141001197 ACTGTGAGCCCGCGGCGTGAGGCGTGGGAGGAAGCGCGGCTGCTGTCGCCCAGCGCCGCCCCGTC ACTGTGAGCCCGCGGCGTGAGGCGTGGGAGGAGGCGCGGCTGCTGTCGCCCAGCGCCGCCCCGTC T C PTK2 Ensembl:ENSG00000169398 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:141000504..141001250;chr8:141000869..141001250;chr8:141000152..141001255;chr8:141000215..141001250;chr8:140984105..141001282 26863196 MeRIP-seq:(Medium) rs1403902982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995746,Human_RBP_ID_5628722,Human_RBP_ID_8923618,Human_RBP_ID_9313622 Human_Splice_Rec_1015913,Human_Splice_Rec_1015975,Human_Splice_Rec_1016185,Human_Splice_Rec_1016293,Human_Splice_Rec_1016357,Human_Splice_Rec_1016781,Human_Splice_Rec_1016799,Human_Splice_Rec_1016807,Human_Splice_Rec_1016825,Human_Splice_Rec_1016853,Human_Splice_Rec_1016867,Human_Splice_Rec_1016873,Human_Splice_Rec_1016879,Human_Splice_Rec_1016883 64538 RMVar_ID_64538 Human_SNP_ID_385249129 m1A Human chr8 + 141001225 141001225 141001225 GCGCTTCCTCCCACGCCTCACGCCGCGGGCTCACAGTGGTCCGGGACCGGCGGCGGCGGCGGCGG GCGCTTCCTCCCACGCCTCACGCCGCGGGCTCGCAGTGGTCCGGGACCGGCGGCGGCGGCGGCGG A G RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:141001176..141001225 32194978 MeRIP-seq:(Medium) rs1220991386 Functional Loss SNV dbSNP153 33..33 33 - - - 64539 RMVar_ID_64539 Human_SNP_ID_385249130 m1A Human chr8 + 141001225 141001225 141001225 GCGCTTCCTCCCACGCCTCACGCCGCGGGCTCACAGTGGTCCGGGACCGGCGGCGGCGGCGGCGG GCGCTTCCTCCCACGCCTCACGCCGCGGGCTCTCAGTGGTCCGGGACCGGCGGCGGCGGCGGCGG A T RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:141001176..141001225 32194978 MeRIP-seq:(Medium) rs1220991386 Functional Loss SNV dbSNP153 33..33 33 - - - 64540 RMVar_ID_64540 Human_SNP_ID_385283919 m1A Human chr8 - 141133866 141133866 141133866 TTCCCCTGACTGCCTCCTGCCACCCCCACTGCACCTCTGGGGTCCCTTAAACTTACGGTCTCAAA TTCCCCTGACTGCCTCCTGCCACCCCCACTGCTCCTCTGGGGTCCCTTAAACTTACGGTCTCAAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:141133859..141134005 26863196 MeRIP-seq:(Medium) rs1021801358 Functional Loss SNV dbSNP153 33..33 33 - - - 64541 RMVar_ID_64541 Human_SNP_ID_385290891 m1A Human chr8 + 141160684 141160684 141160684 ACCATGAGCTGCACGCCGCCCACCTCCTCTCCAGCACAGACCTGAAGGAGGGCCGAGCCCACCGG ACCATGAGCTGCACGCCGCCCACCTCCTCTCCGGCACAGACCTGAAGGAGGGCCGAGCCCACCGG A G DENND3 Ensembl:ENSG00000105339 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:141158275..141160720 32194978 MeRIP-seq:(Medium) rs770365068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1016938,Human_Splice_Rec_1016982,Human_Splice_Rec_1017118 RMVar_hsa_circ_17034,RMVar_hsa_circ_267044,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820,RMVar_hsa_circ_340381,RMVar_hsa_circ_325310,RMVar_hsa_circ_18320,RMVar_hsa_circ_76463,RMVar_hsa_circ_254825,RMVar_hsa_circ_254826,RMVar_hsa_circ_310395,RMVar_hsa_circ_317969,RMVar_hsa_circ_347149,RMVar_hsa_circ_254830,RMVar_hsa_circ_254831,RMVar_hsa_circ_254829,RMVar_hsa_circ_109091,RMVar_hsa_circ_316949,RMVar_hsa_circ_328806,RMVar_hsa_circ_275336,RMVar_hsa_circ_35551,RMVar_hsa_circ_295785,RMVar_hsa_circ_254832,RMVar_hsa_circ_254834,RMVar_hsa_circ_254835,RMVar_hsa_circ_254833,RMVar_hsa_circ_303350,RMVar_hsa_circ_340310,RMVar_hsa_circ_254836,RMVar_hsa_circ_254837 64542 RMVar_ID_64542 Human_SNP_ID_385292779 m1A Human chr8 - 141168126 141168126 141168126 CAGGAGCAGAGAGTTATCGGGGGCCAGAAAGCACATGGCCTCGCTCAGCATGGAGACAAAGTGGG CAGGAGCAGAGAGTTATCGGGGGCCAGAAAGCCCATGGCCTCGCTCAGCATGGAGACAAAGTGGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:141168036..141168163 26863196 MeRIP-seq:(Medium) rs1307554063 Functional Loss SNV dbSNP153 33..33 33 - - - 64543 RMVar_ID_64543 Human_SNP_ID_385292881 m1A Human chr8 + 141168414 141168414 141168414 CCTCGAAGCTGGACGACCACGTGAAGAAGTTCAAGCTGCCCAAGAAGCACATGCAGCTGGGCGAC CCTCGAAGCTGGACGACCACGTGAAGAAGTTCGAGCTGCCCAAGAAGCACATGCAGCTGGGCGAC A G DENND3 Ensembl:ENSG00000105339 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141168363..141168449 26863196 MeRIP-seq:(Medium) rs750158523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820,RMVar_hsa_circ_340381,RMVar_hsa_circ_325310,RMVar_hsa_circ_254825,RMVar_hsa_circ_254826,RMVar_hsa_circ_310395,RMVar_hsa_circ_254831,RMVar_hsa_circ_109091,RMVar_hsa_circ_275336,RMVar_hsa_circ_35551,RMVar_hsa_circ_61547,RMVar_hsa_circ_254832,RMVar_hsa_circ_254833,RMVar_hsa_circ_340310,RMVar_hsa_circ_254837,RMVar_hsa_circ_254838,RMVar_hsa_circ_91637,RMVar_hsa_circ_254839,RMVar_hsa_circ_375354 64544 RMVar_ID_64544 Human_SNP_ID_385293817 m1A Human chr8 + 141171907 141171905 141171907 TGCATGGTGATGGGCATGCACAGTGGGTGTGCACAGTGGCCGAGGGTGTGCATGGTGGTGGTGTG TGCATGGTGATGGGCATGCACAGTGGGTGTG__CAGTGGCCGAGGGTGTGCATGGTGGTGGTGTG GCA G DENND3 Ensembl:ENSG00000105339 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141171903..141172159 26863196 MeRIP-seq:(Medium) rs555435954 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_340381,RMVar_hsa_circ_254826,RMVar_hsa_circ_109091,RMVar_hsa_circ_35551,RMVar_hsa_circ_254832 64545 RMVar_ID_64545 Human_SNP_ID_385293837 m1A Human chr8 + 141171964 141171964 141171964 GTGGTGTGCAGTGTCTGGGTGTGCACTGTGGTAGGTGTGAACAGTGGGTGTGCATGGTGGTGGCC GTGGTGTGCAGTGTCTGGGTGTGCACTGTGGTGGGTGTGAACAGTGGGTGTGCATGGTGGTGGCC A G DENND3 Ensembl:ENSG00000105339 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:141171928..141172087 26863196 MeRIP-seq:(Medium) rs1357399715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_340381,RMVar_hsa_circ_254826,RMVar_hsa_circ_109091,RMVar_hsa_circ_35551,RMVar_hsa_circ_254832 64546 RMVar_ID_64546 Human_SNP_ID_385300409 m1A Human chr8 - 141194112 141194112 141194112 CGGTGTCCATGTGCGCCACCAGCTCCTTCTCCACGGTCTTCCTCTCGGCGTCAATCACGTAGATT CGGTGTCCATGTGCGCCACCAGCTCCTTCTCCCCGGTCTTCCTCTCGGCGTCAATCACGTAGATT T G lnc-SLC45A4-8 RNACentral:URS0000D5D720 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141194061..141194255 26863196 MeRIP-seq:(Medium) rs747754944 Functional Loss SNV dbSNP153 33..33 33 - - - 64547 RMVar_ID_64547 Human_SNP_ID_385300413 m1A Human chr8 + 141194117 141194117 141194117 ACGTGATTGACGCCGAGAGGAAGACCGTGGAGAAGGAGCTGGTGGCGCACATGGACACCGTGAGG ACGTGATTGACGCCGAGAGGAAGACCGTGGAGGAGGAGCTGGTGGCGCACATGGACACCGTGAGG A G DENND3 Ensembl:ENSG00000105339 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:141194066..141194237 26863196 MeRIP-seq:(Medium) rs1208253970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1016966,Human_Splice_Rec_1017010,Human_Splice_Rec_1017072,Human_Splice_Rec_1017112,Human_Splice_Rec_1017160,Human_Splice_Rec_1017166 64548 RMVar_ID_64548 Human_SNP_ID_385300652 m1A Human chr8 - 141194859 141194855 141194859 GTTGCATCTATTAAAAAGAAAAGGGAAAAAAGACAGCTTGCCTCAGCTGGCCCAACCCCTGTCGC GTTGCATCTATTAAAAAGAAAAGGGAAAAAAG____CTTGCCTCAGCTGGCCCAACCCCTGTCGC GCTGT G lnc-SLC45A4-8 RNACentral:URS0000D5D720 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:141194809..141194910 32194978 MeRIP-seq:(Medium) rs1317903569 Functional Loss DEL dbSNP153 33..36 33 - - - 64549 RMVar_ID_64549 Human_SNP_ID_385326719 m1A Human chr8 - 141282434 141282434 141282434 GGAGACAGAGGCTCAGAAGTGCAGTTTGGTGGAGGCGGGGCCGCCCAGCGGGTGAGCTTGACTAG GGAGACAGAGGCTCAGAAGTGCAGTTTGGTGGGGGCGGGGCCGCCCAGCGGGTGAGCTTGACTAG T C SLC45A4 Ensembl:ENSG00000022567 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:141282398..141282650 26863196 MeRIP-seq:(Medium) rs1311253055 Functional Loss SNV dbSNP153 33..33 33 - - - 64550 RMVar_ID_64550 Human_SNP_ID_385361438 m1A Human chr8 + 141405965 141405964 141405965 GGGAGGCAGGTGAGGCTACAGCAGATGAGGAGAGGGGAGTGGTAGGAGGTCAGAGGGCAGGGAGC GGGAGGCAGGTGAGGCTACAGCAGATGAGGAG_GGGGAGTGGTAGGAGGTCAGAGGGCAGGGAGC GA G PTP4A3 Ensembl:ENSG00000184489 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141405946..141406035 26863196 MeRIP-seq:(Medium) rs759159263 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3886004,Human_RBP_ID_8221263,Human_RBP_ID_8238455 64551 RMVar_ID_64551 Human_SNP_ID_385364395 m1A Human chr8 + 141416969 141416969 141416969 GGCCACACCTCCAGGGACCCTGTGCTGGGGGTACCACCCTTGCCGCTCCACCCTGCTCTGAGGGC GGCCACACCTCCAGGGACCCTGTGCTGGGGGTTCCACCCTTGCCGCTCCACCCTGCTCTGAGGGC A T PTP4A3 Ensembl:ENSG00000184489 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:141416962..141417289 32194978 MeRIP-seq:(Medium) rs1350129648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22747305 64552 RMVar_ID_64552 Human_SNP_ID_385370911 m1A Human chr8 - 141435319 141435319 141435319 CCCGCACAGCAGGCTGCCTCCAGTGCCCATGGAGGCCTGTGGCCTCTAGGGGAAAGGGCTCAGAC CCCGCACAGCAGGCTGCCTCCAGTGCCCATGGTGGCCTGTGGCCTCTAGGGGAAAGGGCTCAGAC T A MROH5 Ensembl:ENSG00000226807 Pseudogene intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:141435269..141435379 32194978 MeRIP-seq:(Medium) rs1193742307 Functional Loss SNV dbSNP153 33..33 33 - - - 64553 RMVar_ID_64553 Human_SNP_ID_385451311 m1A Human chr8 - 141713828 141713828 141713828 CCACCACCATCATCACCACCACCACCATCACCATCATCATCATCACCATCACCATCACCACCACC CCACCACCATCATCACCACCACCACCATCACCGTCATCATCATCACCATCACCATCACCACCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141713778..141713902 26863196 MeRIP-seq:(Medium) rs377075147 Functional Loss SNV dbSNP153 33..33 33 - - - 64554 RMVar_ID_64554 Human_SNP_ID_385451482 m1A Human chr8 - 141714043 141714043 141714043 TCATCACCATCACCATCATCACTACCATCACCATCATCATCACCATCACCATCATCACCACCATC TCATCACCATCACCATCATCACTACCATCACCCTCATCATCACCATCACCATCATCACCACCATC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:141714019..141714103 26863196 MeRIP-seq:(Medium) rs1173152741 Functional Loss SNV dbSNP153 33..33 33 - - - 64555 RMVar_ID_64555 Human_SNP_ID_385451492 m1A Human chr8 + 141714066 141714065 141714066 TGATGATGATGGTGATGGTAGTGATGATGGTGATGGTGATGATGATGGTGATGGTGATGGTGGTG TGATGATGATGGTGATGGTAGTGATGATGGTG_TGGTGATGATGATGGTGATGGTGATGGTGGTG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141714018..141714104 26863196 MeRIP-seq:(Medium) rs1278708596 Functional Loss DEL dbSNP153 33..33 33 - - - 64556 RMVar_ID_64556 Human_SNP_ID_385451493 m1A Human chr8 + 141714066 141714066 141714066 TGATGATGATGGTGATGGTAGTGATGATGGTGATGGTGATGATGATGGTGATGGTGATGGTGGTG TGATGATGATGGTGATGGTAGTGATGATGGTGGTGGTGATGATGATGGTGATGGTGATGGTGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:141714018..141714104 26863196 MeRIP-seq:(Medium) rs1201591003 Functional Loss SNV dbSNP153 33..33 33 - - - 64557 RMVar_ID_64557 Human_SNP_ID_385612924 m1A Human chr8 - 142272195 142272194 142272196 AGGAGTAGATGGGTGAGTGGCTGGGTGGATGGACAGACAGCATGGATAAATGGGTGAGTAGACGG AGGAGTAGATGGGTGAGTGGCTGGGTGGATG__CAGACAGCATGGATAAATGGGTGAGTAGACGG GTC G TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:142272005..142272618 26863196 MeRIP-seq:(Medium) rs1420377113 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_268000,Human_RBP_ID_8221315,Human_RBP_ID_9441227,Human_RBP_ID_24249050 RMVar_hsa_circ_1775,RMVar_hsa_circ_85726,RMVar_hsa_circ_102029,RMVar_hsa_circ_254850,RMVar_hsa_circ_20984,RMVar_hsa_circ_254851 64558 RMVar_ID_64558 Human_SNP_ID_385612939 m1A Human chr8 + 142272250 142272250 142272250 ATCTACTCCTTCCTCCTTCCATCTACCCATCCACCTGCCCGTCTACACCTTCCTCCTTCCACCTA ATCTACTCCTTCCTCCTTCCATCTACCCATCCCCCTGCCCGTCTACACCTTCCTCCTTCCACCTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:142272199..142272374 26863196 MeRIP-seq:(Medium) rs950492257 Functional Loss SNV dbSNP153 33..33 33 - - - 64559 RMVar_ID_64559 Human_SNP_ID_385613089 m1A Human chr8 + 142272506 142272506 142272506 GCCCGTCTACACCTTCCTTCTTCCATCCATCCACCACCCGTCTACAGCTTCCTCCTTCCATCTAC GCCCGTCTACACCTTCCTTCTTCCATCCATCCCCCACCCGTCTACAGCTTCCTCCTTCCATCTAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:142272459..142272550 26863196 MeRIP-seq:(Medium) rs1338899706 Functional Loss SNV dbSNP153 33..33 33 - - - 64560 RMVar_ID_64560 Human_SNP_ID_385613093 m1A Human chr8 - 142272514 142272511 142272514 ACAGGTGGGTAGATGGAAGGAGGAAGCTGTAGACGGGTGGTGGATGGATGGAAGAAGGAAGGTGT ACAGGTGGGTAGATGGAAGGAGGAAGCTGTAG___GGTGGTGGATGGATGGAAGAAGGAAGGTGT CCGT C TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:142271946..142272629 26863196 MeRIP-seq:(Medium) rs1225941995 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_268161,Human_RBP_ID_24249056 RMVar_hsa_circ_1775,RMVar_hsa_circ_85726,RMVar_hsa_circ_102029,RMVar_hsa_circ_254850,RMVar_hsa_circ_20984,RMVar_hsa_circ_254851 64561 RMVar_ID_64561 Human_SNP_ID_385613097 m1A Human chr8 - 142272514 142272514 142272514 ACAGGTGGGTAGATGGAAGGAGGAAGCTGTAGACGGGTGGTGGATGGATGGAAGAAGGAAGGTGT ACAGGTGGGTAGATGGAAGGAGGAAGCTGTAGGCGGGTGGTGGATGGATGGAAGAAGGAAGGTGT T C TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:142271946..142272629 26863196 MeRIP-seq:(Medium) rs1337181338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268161,Human_RBP_ID_24249056 RMVar_hsa_circ_1775,RMVar_hsa_circ_85726,RMVar_hsa_circ_102029,RMVar_hsa_circ_254850,RMVar_hsa_circ_20984,RMVar_hsa_circ_254851 64562 RMVar_ID_64562 Human_SNP_ID_385613642 m1A Human chr8 + 142273962 142273962 142273962 CTGCTCCTGGACCCTGGCCTCACACCCACTGCACCATCTCGTCTGCCAATACTGCCCCTGCTCCG CTGCTCCTGGACCCTGGCCTCACACCCACTGCCCCATCTCGTCTGCCAATACTGCCCCTGCTCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:142273912..142274016 26863196 MeRIP-seq:(Medium) rs1474103630 Functional Loss SNV dbSNP153 33..33 33 - - - 64563 RMVar_ID_64563 Human_SNP_ID_385613644 m1A Human chr8 - 142273966 142273966 142273966 AGGGCGGAGCAGGGGCAGTATTGGCAGACGAGATGGTGCAGTGGGTGTGAGGCCAGGGTCCAGGA AGGGCGGAGCAGGGGCAGTATTGGCAGACGAGTTGGTGCAGTGGGTGTGAGGCCAGGGTCCAGGA T A TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142273854..142274038 26863196 MeRIP-seq:(Medium) rs1247983896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3887169,Human_RBP_ID_22731633 RMVar_hsa_circ_1775,RMVar_hsa_circ_85726,RMVar_hsa_circ_102029,RMVar_hsa_circ_254850,RMVar_hsa_circ_20984,RMVar_hsa_circ_254851 64564 RMVar_ID_64564 Human_SNP_ID_385622757 m1A Human chr8 + 142300529 142300529 142300529 GGATGGCCTCCTCCCGCAGCCGGATGGCCTCCAGGTCCTCTTCAGTGATGTCCGGGAGCAGCGCC GGATGGCCTCCTCCCGCAGCCGGATGGCCTCCGGGTCCTCTTCAGTGATGTCCGGGAGCAGCGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:142300431..142300557 26863196 MeRIP-seq:(Medium) rs750534638 Functional Loss SNV dbSNP153 33..33 33 - - - 64565 RMVar_ID_64565 Human_SNP_ID_385644193 m1A Human chr8 - 142372867 142372867 142372867 AACAGCACTGGTGGGGTGGCCTTCTCAGGAGGAGGCCTGGGGGAGTCTGCTGGGAGAGGCACAGC AACAGCACTGGTGGGGTGGCCTTCTCAGGAGGTGGCCTGGGGGAGTCTGCTGGGAGAGGCACAGC T A TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142372862..142372938 26863196 MeRIP-seq:(Medium) rs1444353812 Functional Loss SNV dbSNP153 33..33 33 - - - 64566 RMVar_ID_64566 Human_SNP_ID_385644194 m1A Human chr8 - 142372867 142372867 142372867 AACAGCACTGGTGGGGTGGCCTTCTCAGGAGGAGGCCTGGGGGAGTCTGCTGGGAGAGGCACAGC AACAGCACTGGTGGGGTGGCCTTCTCAGGAGGCGGCCTGGGGGAGTCTGCTGGGAGAGGCACAGC T G TSNARE1 Ensembl:ENSG00000171045 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142372862..142372938 26863196 MeRIP-seq:(Medium) rs1444353812 Functional Loss SNV dbSNP153 33..33 33 - - - 64567 RMVar_ID_64567 Human_SNP_ID_385652742 m1A Human chr8 + 142402941 142402911 142402941 CCCCCGGCACGGTCCCGCCCCCTCCCCTCCCCACCGGCGCGGCCCCGCCCCCCGCCCGGCCTCCC CCC______________________________CCGGCGCGGCCCCGCCCCCCGCCCGGCCTCCC CCCGGCACGGTCCCGCCCCCTCCCCTCCCCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:142402922..142403049 26863196 MeRIP-seq:(Medium) rs1313887603 Functional Loss DEL dbSNP153 4..33 33 - - - 64568 RMVar_ID_64568 Human_SNP_ID_385652761 m1A Human chr8 + 142402941 142402941 142402941 CCCCCGGCACGGTCCCGCCCCCTCCCCTCCCCACCGGCGCGGCCCCGCCCCCCGCCCGGCCTCCC CCCCCGGCACGGTCCCGCCCCCTCCCCTCCCCCCCGGCGCGGCCCCGCCCCCCGCCCGGCCTCCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:142402922..142403049 26863196 MeRIP-seq:(Medium) rs1180090005 Functional Loss SNV dbSNP153 33..33 33 - - - 64569 RMVar_ID_64569 Human_SNP_ID_385652789 m1A Human chr8 + 142402993 142402993 142402993 CGCCCGGCCTCCCGCAAGCCCCATACCACGCCACGCCGCGGCCCCCGCCGGGCTCCGGGCCCCGC CGCCCGGCCTCCCGCAAGCCCCATACCACGCCGCGCCGCGGCCCCCGCCGGGCTCCGGGCCCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:142402987..142403160 26863196 MeRIP-seq:(Medium) rs1472876731 Functional Loss SNV dbSNP153 33..33 33 - - - 64570 RMVar_ID_64570 Human_SNP_ID_385695989 m1A Human chr8 - 142542031 142542031 142542031 TGAAATTGGTGGGCGGCCCCTTGGCATGGGCCAGCTTCAGCTTCTCCTCCTCGGGCAGAGACGGC TGAAATTGGTGGGCGGCCCCTTGGCATGGGCCGGCTTCAGCTTCTCCTCCTCGGGCAGAGACGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142541941..142542041 32194978 MeRIP-seq:(Medium) rs1411697512 Functional Loss SNV dbSNP153 33..33 33 - - - 64571 RMVar_ID_64571 Human_SNP_ID_385696117 m1A Human chr8 + 142542319 142542319 142542319 CACGGCCACGCTGCGGCCCAAGCCCAAGGAGGAGCCCAAGTACAGCATCCACATTGACCAGATGC CACGGCCACGCTGCGGCCCAAGCCCAAGGAGGGGCCCAAGTACAGCATCCACATTGACCAGATGC A G ADGRB1 Ensembl:ENSG00000181790 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:142542271..142542415 26863196 MeRIP-seq:(Medium) rs1338397330 Functional Loss SNV dbSNP153 33..33 33 - - - 64572 RMVar_ID_64572 Human_SNP_ID_385729976 m1A Human chr8 + 142660381 142660381 142660381 CCTACCTCATGACCTCCCCGACCCTGATCTCCACACCTGACCCCAAAGCACATTTTGTTATTTTT CCTACCTCATGACCTCCCCGACCCTGATCTCCGCACCTGACCCCAAAGCACATTTTGTTATTTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:142660330..142660406;chr8:142660275..142660507;chr8:142660331..142660470 26863196 MeRIP-seq:(Medium) rs587770067 Functional Loss SNV dbSNP153 33..33 33 - - - 64573 RMVar_ID_64573 Human_SNP_ID_385731265 m1A Human chr8 - 142664596 142664596 142664596 AGATCCTGGTGAGGGCGAGGAGGTGGCCTGGGAGCAGGCGGCCGTGGCCTTTGACGCAGTCCTGC AGATCCTGGTGAGGGCGAGGAGGTGGCCTGGGCGCAGGCGGCCGTGGCCTTTGACGCAGTCCTGC T G JRK Ensembl:ENSG00000234616 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:142664548..142664686 26863196 MeRIP-seq:(Medium) rs782805783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845358,Human_RBP_ID_22731637 64574 RMVar_ID_64574 Human_SNP_ID_385736225 m1A Human chr8 + 142680516 142680516 142680516 CCCTCTCCACCACAGCCCACCAGTGACCACGAAGGCTGTGCTGCTTGCCCTGTTGATGGCAGGCT CCCTCTCCACCACAGCCCACCAGTGACCACGAGGGCTGTGCTGCTTGCCCTGTTGATGGCAGGCT A G PSCA Ensembl:ENSG00000167653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142680466..142680752 26863196 MeRIP-seq:(Medium) rs1394311286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1018063,Human_Splice_Rec_1018065 64575 RMVar_ID_64575 Human_SNP_ID_385736304 m1A Human chr8 + 142680731 142680731 142680731 GCCTCCGCTCCTCCAGGGAAGCTCTTGGCACGACCAGGCAGCGACCTGTTCCCTGCCGTCCCCTG GCCTCCGCTCCTCCAGGGAAGCTCTTGGCACGTCCAGGCAGCGACCTGTTCCCTGCCGTCCCCTG A T PSCA Ensembl:ENSG00000167653 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142680488..142681496 32194978 MeRIP-seq:(Medium) rs1014700254 Functional Loss SNV dbSNP153 33..33 33 - - - 64576 RMVar_ID_64576 Human_SNP_ID_385736613 m1A Human chr8 + 142681570 142681570 142681570 CCCCGACCCGTCCCGCACCTGCACCCCCAACAATCACCCAGCATCTGTCCCTCCAGCCATCCTCC CCCCGACCCGTCCCGCACCTGCACCCCCAACAGTCACCCAGCATCTGTCCCTCCAGCCATCCTCC A G PSCA Ensembl:ENSG00000167653 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:142681523..142681652 26863196 MeRIP-seq:(Medium) rs1378028158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124041,RMVar_hsa_circ_254872 64577 RMVar_ID_64577 Human_SNP_ID_385742320 m1A Human chr8 - 142703201 142703201 142703201 GTAGCGAATTTTACAACACTTGAGGTAAAAGAAGGGCATGGGCTCTTCCAGGAGAAACCGCTTCT GTAGCGAATTTTACAACACTTGAGGTAAAAGAGGGGCATGGGCTCTTCCAGGAGAAACCGCTTCT T C LNCOC1 Ensembl:ENSG00000253741 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142703150..142703375 26863196 MeRIP-seq:(Medium) rs142496379 Functional Loss SNV dbSNP153 33..33 33 - - - 64578 RMVar_ID_64578 Human_SNP_ID_385748083 m1A Human chr8 + 142727771 142727771 142727771 CTACCTGGAGGCGCGCTTTGTCAGCCTGCGGGACGGCTTCGTGTGCGCGCTGCTGCGCTTCCGGC CTACCTGGAGGCGCGCTTTGTCAGCCTGCGGGGCGGCTTCGTGTGCGCGCTGCTGCGCTTCCGGC A G THEM6 Ensembl:ENSG00000130193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142727651..142727875 32194978 MeRIP-seq:(Medium) rs1467857712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695341,Human_RBP_ID_22115912,Human_RBP_ID_22775768 Human_Splice_Rec_1018145,Human_Splice_Rec_1018147 RMVar_hsa_circ_91157,RMVar_hsa_circ_124301,RMVar_hsa_circ_254874,RMVar_hsa_circ_254875 64579 RMVar_ID_64579 Human_SNP_ID_385748084 m1A Human chr8 + 142727771 142727771 142727771 CTACCTGGAGGCGCGCTTTGTCAGCCTGCGGGACGGCTTCGTGTGCGCGCTGCTGCGCTTCCGGC CTACCTGGAGGCGCGCTTTGTCAGCCTGCGGGTCGGCTTCGTGTGCGCGCTGCTGCGCTTCCGGC A T THEM6 Ensembl:ENSG00000130193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142727651..142727875 32194978 MeRIP-seq:(Medium) rs1467857712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695341,Human_RBP_ID_22115912,Human_RBP_ID_22775768 Human_Splice_Rec_1018145,Human_Splice_Rec_1018147 RMVar_hsa_circ_91157,RMVar_hsa_circ_124301,RMVar_hsa_circ_254874,RMVar_hsa_circ_254875 64580 RMVar_ID_64580 Human_SNP_ID_385749938 m1A Human chr8 - 142734435 142734435 142734435 CAGAGTCTCTGCTGTTCTGGGTCCCAGCCTTCACCTCCCACAGGGACCTCACCAACCAGCCCATG CAGAGTCTCTGCTGTTCTGGGTCCCAGCCTTCGCCTCCCACAGGGACCTCACCAACCAGCCCATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:142734408..142734637 26863196 MeRIP-seq:(Medium) rs1293782330 Functional Loss SNV dbSNP153 33..33 33 - - - 64581 RMVar_ID_64581 Human_SNP_ID_385750365 m1A Human chr8 - 142736085 142736082 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGT___GGAGGAGGAGGAGGCAAGGCCGACTGCAGT CTCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs1233280862 Functional Loss DEL dbSNP153 33..35 33 - - - 64582 RMVar_ID_64582 Human_SNP_ID_385750368 m1A Human chr8 - 142736085 142736085 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTTGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs3736010 Functional Loss SNV dbSNP153 33..33 33 - - - 64583 RMVar_ID_64583 Human_SNP_ID_385750369 m1A Human chr8 - 142736085 142736085 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTGGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs3736010 Functional Loss SNV dbSNP153 33..33 33 - - - 64584 RMVar_ID_64584 Human_SNP_ID_385750370 m1A Human chr8 - 142736085 142736085 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTCGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs3736010 Functional Loss SNV dbSNP153 33..33 33 - - - 64585 RMVar_ID_64585 Human_SNP_ID_385750529 m1A Human chr8 + 142736726 142736726 142736726 TCAGGGCCCTGTGCCCGCTTGCCTGTTCCCCTACATCTGTGCCTGCACATCCAGAACTGCCTCCT TCAGGGCCCTGTGCCCGCTTGCCTGTTCCCCTGCATCTGTGCCTGCACATCCAGAACTGCCTCCT A G THEM6 Ensembl:ENSG00000130193 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142736676..142736750 32194978 MeRIP-seq:(Medium) rs891064200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123526,Human_RBP_ID_22372494,Human_RBP_ID_26558338 RMVar_hsa_circ_91157,RMVar_hsa_circ_124301,RMVar_hsa_circ_254874,RMVar_hsa_circ_92662,RMVar_hsa_circ_254875,RMVar_hsa_circ_254876 64586 RMVar_ID_64586 Human_SNP_ID_385752645 m1A Human chr8 - 142744131 142744128 142744132 CATCCCCCATCCATCCACCCATCCATCCATCTATCCATCTACCCATCCAGCCATCTATCCATCCC CATCCCCCATCCATCCACCCATCCATCCATC____CATCTACCCATCCAGCCATCTATCCATCCC GGATA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:142744128..142744310 26863196 MeRIP-seq:(Medium) rs1296293334 Functional Loss DEL dbSNP153 32..35 33 - - - 64587 RMVar_ID_64587 Human_SNP_ID_385753015 m1A Human chr8 - 142745058 142745058 142745058 TCCTCTGCCCATCCACCCATCCGTCCCCATCCATCCACTCATCCTCCCCTCATCCCCCACGCATC TCCTCTGCCCATCCACCCATCCGTCCCCATCCGTCCACTCATCCTCCCCTCATCCCCCACGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142745043..142745155 26863196 MeRIP-seq:(Medium) rs1404364116 Functional Loss SNV dbSNP153 33..33 33 - - - 64588 RMVar_ID_64588 Human_SNP_ID_385829403 m1A Human chr8 - 143018565 143018565 143018565 CGCGGACTCACCGCCGGGCGGACGCAGGTACCAGCAGCCTGGCCGAGCTCCCCGAACCTCGCGCG CGCGGACTCACCGCCGGGCGGACGCAGGTACCGGCAGCCTGGCCGAGCTCCCCGAACCTCGCGCG T C LY6E-DT RNACentral:URS00009B539C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143018476..143018860;chr8:143018476..143018960;chr8:143018476..143018644 26863196 MeRIP-seq:(Medium) rs1318632301 Functional Loss SNV dbSNP153 33..33 33 - - - 64589 RMVar_ID_64589 Human_SNP_ID_385830076 m1A Human chr8 - 143020863 143020862 143020863 AGCCTGTCCTGCTCTGGAGAGACACACTGGTTAGGGGGCCGGGTGGTGCCTCACTCCTCCCCAAG AGCCTGTCCTGCTCTGGAGAGACACACTGGTT_GGGGGCCGGGTGGTGCCTCACTCCTCCCCAAG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143020855..143021008 26863196 MeRIP-seq:(Medium) rs1420747216 Functional Loss DEL dbSNP153 33..33 33 - - - 64590 RMVar_ID_64590 Human_SNP_ID_385830083 m1A Human chr8 + 143020881 143020881 143020881 ACCACCCGGCCCCCTAACCAGTGTGTCTCTCCAGAGCAGGACAGGCTGCTTTGGTTTGTGACCTC ACCACCCGGCCCCCTAACCAGTGTGTCTCTCCGGAGCAGGACAGGCTGCTTTGGTTTGTGACCTC A G LY6E Ensembl:ENSG00000160932 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143020876..143020900 26863196 MeRIP-seq:(Medium) rs1450825014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82279,RMVar_hsa_circ_98168,RMVar_hsa_circ_254880,RMVar_hsa_circ_254881,RMVar_hsa_circ_102792 64591 RMVar_ID_64591 Human_SNP_ID_385830282 m1A Human chr8 - 143021423 143021423 143021423 CGGTCTGAGGCCTGGCACTCACCAATGCCGGCACTAGCAGACACAGTCACGCAGTAGTTGTCCTG CGGTCTGAGGCCTGGCACTCACCAATGCCGGCCCTAGCAGACACAGTCACGCAGTAGTTGTCCTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:143021376..143021450 32194978 MeRIP-seq:(Medium) rs535909345 Functional Loss SNV dbSNP153 33..33 33 - - - 64592 RMVar_ID_64592 Human_SNP_ID_385830453 m1A Human chr8 + 143021798 143021798 143021798 GCCCTGCTGCGGTTTGGCCCCTGACCGCCCAGACCCTGTCCCCCGATCCCCCAGCTCAGGAAGGA GCCCTGCTGCGGTTTGGCCCCTGACCGCCCAGTCCCTGTCCCCCGATCCCCCAGCTCAGGAAGGA A T LY6E Ensembl:ENSG00000160932 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143021716..143021902 26863196 MeRIP-seq:(Medium) rs1283532866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254942,Human_RBP_ID_695379,Human_RBP_ID_5123527,Human_RBP_ID_17320337,Human_RBP_ID_17666021,Human_RBP_ID_18961217,Human_RBP_ID_22465311,Human_RBP_ID_22776116,Human_RBP_ID_24537253,Human_RBP_ID_26558339,Human_RBP_ID_27536225 Human_miRNA_ID_2653197,Human_miRNA_ID_2653198,Human_miRNA_ID_2754394,Human_miRNA_ID_2754395 RMVar_hsa_circ_98168,RMVar_hsa_circ_254881,RMVar_hsa_circ_102792,RMVar_hsa_circ_254882,RMVar_hsa_circ_83783,RMVar_hsa_circ_125857,RMVar_hsa_circ_93920,RMVar_hsa_circ_254883,RMVar_hsa_circ_254886,RMVar_hsa_circ_100030,RMVar_hsa_circ_254887,RMVar_hsa_circ_254888 64593 RMVar_ID_64593 Human_SNP_ID_385830469 m1A Human chr8 + 143021837 143021836 143021837 CCCCCGATCCCCCAGCTCAGGAAGGAAAGCCCAGCCCTTTCTGGATCCCACAGTGTATGGGAGCC CCCCCGATCCCCCAGCTCAGGAAGGAAAGCCC_GCCCTTTCTGGATCCCACAGTGTATGGGAGCC CA C LY6E Ensembl:ENSG00000160932 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr8:143021568..143022374;chr8:143021701..143022025;chr8:143021631..143021997 26863196 MeRIP-seq:(Medium) rs745674413 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_254942,Human_RBP_ID_695379,Human_RBP_ID_1400741,Human_RBP_ID_5123815,Human_RBP_ID_17320337,Human_RBP_ID_17666021,Human_RBP_ID_18961217,Human_RBP_ID_24537253,Human_RBP_ID_26558339 Human_miRNA_ID_1159884,Human_miRNA_ID_1360956,Human_miRNA_ID_2553666,Human_miRNA_ID_2553667 RMVar_hsa_circ_98168,RMVar_hsa_circ_254881,RMVar_hsa_circ_102792,RMVar_hsa_circ_254882,RMVar_hsa_circ_83783,RMVar_hsa_circ_125857,RMVar_hsa_circ_93920,RMVar_hsa_circ_254883,RMVar_hsa_circ_254886,RMVar_hsa_circ_100030,RMVar_hsa_circ_254887,RMVar_hsa_circ_254888 64594 RMVar_ID_64594 Human_SNP_ID_385830485 m1A Human chr8 - 143021904 143021904 143021904 GGTGGAGGTGCAGGGGGTGGGCCTGACCTGGGACCAAGGGCACAGATCAGGCACGTGAGGAGTCA GGTGGAGGTGCAGGGGGTGGGCCTGACCTGGGGCCAAGGGCACAGATCAGGCACGTGAGGAGTCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143021688..143022050 26863196 MeRIP-seq:(Medium) rs1427671850 Functional Loss SNV dbSNP153 33..33 33 - - - 64595 RMVar_ID_64595 Human_SNP_ID_385830590 m1A Human chr8 - 143022327 143022327 143022327 ATGTGGGGGTGGGCTGGGGCAGGACTGGCTGGATTTGGGGCAGGGCCTAGACCCGGAAGTGGCAG ATGTGGGGGTGGGCTGGGGCAGGACTGGCTGGGTTTGGGGCAGGGCCTAGACCCGGAAGTGGCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:143022276..143022400 32194978 MeRIP-seq:(Medium) rs980376608 Functional Loss SNV dbSNP153 33..33 33 - - - 64596 RMVar_ID_64596 Human_SNP_ID_385900432 m1A Human chr8 - 143261424 143261424 143261424 TCCCTGGACCTCAGCTGTTCCTCATTGACCTCAGAGACACCCTGCCCTGCCCCGGCTTCTCAGGA TCCCTGGACCTCAGCTGTTCCTCATTGACCTCGGAGACACCCTGCCCTGCCCCGGCTTCTCAGGA T C RF00017-4575,lnc-TOP1MT-5 RNACentral:URS0000918622,RNACentral:URS00008C3544 SRP RNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143261358..143261543 26863196 MeRIP-seq:(Medium) rs1045667203 Functional Loss SNV dbSNP153 33..33 33 - - - 64597 RMVar_ID_64597 Human_SNP_ID_385900728 m1A Human chr8 - 143262045 143262004 143262045 AGGTGCGGGCGCGGGCAGGGGCTGCCGGAGACAGCCGTGAGGGGTGCGGGTGCAGGCAGGGGCTG AGGTGCGGGCGCGGGCAGGGGCTGCCGGAGAC_________________________________ CGTCTCCGGCAGCCCCTGCCTGCACCCGCACCCCTCACGGCT C RF00017-4575,lnc-TOP1MT-5 RNACentral:URS0000918622,RNACentral:URS00008C3544 SRP RNA,lincRNA intron,exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:143261959..143262075 26863410 MeRIP-seq:(Medium) rs1563731624 Functional Loss DEL dbSNP153 33..65 33 - - - 64598 RMVar_ID_64598 Human_SNP_ID_385900761 m1A Human chr8 - 143262045 143262045 143262045 AGGTGCGGGCGCGGGCAGGGGCTGCCGGAGACAGCCGTGAGGGGTGCGGGTGCAGGCAGGGGCTG AGGTGCGGGCGCGGGCAGGGGCTGCCGGAGACGGCCGTGAGGGGTGCGGGTGCAGGCAGGGGCTG T C RF00017-4575,lnc-TOP1MT-5 RNACentral:URS0000918622,RNACentral:URS00008C3544 SRP RNA,lincRNA intron,exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:143261959..143262075 26863410 MeRIP-seq:(Medium) rs1172596269 Functional Loss SNV dbSNP153 33..33 33 - - - 64599 RMVar_ID_64599 Human_SNP_ID_385902496 m1A Human chr8 + 143267845 143267824 143267845 CGGAGCGAGGAGCCGCCGGACCCCAGCGCCGCACCGCCGGGCGGACGCGCTCTGTGCCGAGCTCC CGGAGCGAGGAG_____________________CCGCCGGGCGGACGCGCTCTGTGCCGAGCTCC GCCGCCGGACCCCAGCGCCGCA G AC138696.1,GLI4 Ensembl:ENSG00000264668,Ensembl:ENSG00000250571 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143267839..143267938 26863196 MeRIP-seq:(Medium) rs1369660993 Functional Loss DEL dbSNP153 13..33 33 - - - 64600 RMVar_ID_64600 Human_SNP_ID_385905035 m1A Human chr8 - 143275755 143275755 143275755 CAAGGAGGGGCCAGGCACCCAGTGGATGGGAGACAAGCGGACAGGGGCTCGGAGTGCCGTGCCCA CAAGGAGGGGCCAGGCACCCAGTGGATGGGAGTCAAGCGGACAGGGGCTCGGAGTGCCGTGCCCA T A RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143275714..143275843 26863196 MeRIP-seq:(Medium) rs1429622599 Functional Loss SNV dbSNP153 33..33 33 - - - 64601 RMVar_ID_64601 Human_SNP_ID_385905650 m1A Human chr8 + 143276782 143276782 143276782 CTTCGGCCAGAGCTCCCAGCTCATCCAGCACCAGCGGGTGCACTACCGCGAGTAGCCGGGCGGGG CTTCGGCCAGAGCTCCCAGCTCATCCAGCACCGGCGGGTGCACTACCGCGAGTAGCCGGGCGGGG A G GLI4 Ensembl:ENSG00000250571 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143276733..143276832 32194978 MeRIP-seq:(Medium) rs773136057 Functional Loss SNV dbSNP153 33..33 33 - - - 64602 RMVar_ID_64602 Human_SNP_ID_385915118 m1A Human chr8 - 143307503 143307503 143307503 ACGCGGGACCCTCTGCCGCCCTCTCCTCTGCCACGCGGGACCCTCTGCCGCCCTCTGCTATGCGG ACGCGGGACCCTCTGCCGCCCTCTCCTCTGCCGCGCGGGACCCTCTGCCGCCCTCTGCTATGCGG T C TOP1MT Ensembl:ENSG00000184428 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143307492..143307667 26863196 MeRIP-seq:(Medium) rs555004719 Functional Loss SNV dbSNP153 33..33 33 - - - 64603 RMVar_ID_64603 Human_SNP_ID_385915231 m1A Human chr8 + 143307804 143307728 143307804 AGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGCAGAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG _________________________________GAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG GAAGAGGGCGGCAGAGGAGAGGGCAGCAGAGGGTCCCGCGTGGCAGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143307717..143307841 26863196 MeRIP-seq:(Medium) rs1554618048 Functional Loss DEL dbSNP153 1..33 33 - - - 64604 RMVar_ID_64604 Human_SNP_ID_385915249 m1A Human chr8 + 143307804 143307790 143307804 AGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGCAGAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG AGAGAAGAGGGCGGCAGAG______________GAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG GGGTCCTGCGTGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143307717..143307841 26863196 MeRIP-seq:(Medium) rs369283627 Functional Loss DEL dbSNP153 20..33 33 - - - 64605 RMVar_ID_64605 Human_SNP_ID_385915254 m1A Human chr8 + 143307804 143307803 143307805 AGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGCAGAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG AGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGC__AGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143307717..143307841 26863196 MeRIP-seq:(Medium) rs1491450290 Functional Loss DEL dbSNP153 33..34 33 - - - 64606 RMVar_ID_64606 Human_SNP_ID_385915547 m1A Human chr8 + 143308384 143308384 143308384 AGAGAAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAGAAGAGGGCGGCAGAGGGTCCCGCGTGGCA AGAGAAGAGGGCGGCAGAGGGTCCCGCGTGGCGGAGAAGAGGGCGGCAGAGGGTCCCGCGTGGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143308319..143308542 26863196 MeRIP-seq:(Medium) rs1382934683 Functional Loss SNV dbSNP153 33..33 33 - - - 64607 RMVar_ID_64607 Human_SNP_ID_385916291 m1A Human chr8 - 143310152 143310152 143310152 GCTGCAGGAGCAGCTGGCGCAGCTGAGTGTGCAGGCCACGGACAAGGAGGAGAACAAGCAGGTGG GCTGCAGGAGCAGCTGGCGCAGCTGAGTGTGCCGGCCACGGACAAGGAGGAGAACAAGCAGGTGG T G TOP1MT Ensembl:ENSG00000184428 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143310065..143310265 26863196 MeRIP-seq:(Medium) rs377037345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5154124,Human_RBP_ID_9405833,Human_RBP_ID_19023100,Human_RBP_ID_26359405,Human_RBP_ID_27832185 Human_Splice_Rec_1018662,Human_Splice_Rec_1018663,Human_Splice_Rec_1018690,Human_Splice_Rec_1018691,Human_Splice_Rec_1018693,Human_Splice_Rec_1018720,Human_Splice_Rec_1018721,Human_Splice_Rec_1018746,Human_Splice_Rec_1018747,Human_Splice_Rec_1018774,Human_Splice_Rec_1018775 RMVar_hsa_circ_64222,RMVar_hsa_circ_81378,RMVar_hsa_circ_254890 64608 RMVar_ID_64608 Human_SNP_ID_385917848 m1A Human chr8 + 143315778 143315778 143315778 CTTGGGCTTTGTGCTCAGCCCTCGCCCTCCTCAGCTCTGCCCTGGCCTCAGCCACCTGCTCCTTC CTTGGGCTTTGTGCTCAGCCCTCGCCCTCCTCCGCTCTGCCCTGGCCTCAGCCACCTGCTCCTTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143315687..143316174 26863196 MeRIP-seq:(Medium) rs1390291631 Functional Loss SNV dbSNP153 33..33 33 - - - 64609 RMVar_ID_64609 Human_SNP_ID_385917849 m1A Human chr8 + 143315778 143315778 143315778 CTTGGGCTTTGTGCTCAGCCCTCGCCCTCCTCAGCTCTGCCCTGGCCTCAGCCACCTGCTCCTTC CTTGGGCTTTGTGCTCAGCCCTCGCCCTCCTCGGCTCTGCCCTGGCCTCAGCCACCTGCTCCTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143315687..143316174 26863196 MeRIP-seq:(Medium) rs1390291631 Functional Loss SNV dbSNP153 33..33 33 - - - 64610 RMVar_ID_64610 Human_SNP_ID_385917943 m1A Human chr8 + 143316022 143316022 143316022 AGCTGCTACCTTCGTCTGGAGATTCTGCATCGACTTCTCGAACGTACTGGGGGTTGCTCGCTGAT AGCTGCTACCTTCGTCTGGAGATTCTGCATCGGCTTCTCGAACGTACTGGGGGTTGCTCGCTGAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143310463..143316100 26863196 MeRIP-seq:(Medium) rs1216789841 Functional Loss SNV dbSNP153 33..33 33 - - - 64611 RMVar_ID_64611 Human_SNP_ID_385918473 m1A Human chr8 - 143317683 143317683 143317683 TGCCCCACACCCACACTCAGCGCGGGGGGAGCACGGCCCCTGCCCCAGACCGGGCTCCCCGGCTG TGCCCCACACCCACACTCAGCGCGGGGGGAGCGCGGCCCCTGCCCCAGACCGGGCTCCCCGGCTG T C TOP1MT Ensembl:ENSG00000184428 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143317682..143317768 26863196 MeRIP-seq:(Medium) rs1163373120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64222,RMVar_hsa_circ_81378,RMVar_hsa_circ_254890 64612 RMVar_ID_64612 Human_SNP_ID_385924123 m1A Human chr8 + 143329348 143329348 143329348 CAGGACAGCTGTGGCGGCCGCCCAGGGTACCTACCTTTCGCCAGTCATTGAAGAAGTTCTTCCGG CAGGACAGCTGTGGCGGCCGCCCAGGGTACCTCCCTTTCGCCAGTCATTGAAGAAGTTCTTCCGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143329338..143329528 26863196 MeRIP-seq:(Medium) rs773764755 Functional Loss SNV dbSNP153 33..33 33 - - - 64613 RMVar_ID_64613 Human_SNP_ID_385924800 m1A Human chr8 - 143331331 143331329 143331332 GACACGTCCTGTCTCCGTCTTTAGGTGGGAGAAGGAGAAGCACGAAGACGGGGTGAAGTGGAGAC GACACGTCCTGTCTCCGTCTTTAGGTGGGAG___GAGAAGCACGAAGACGGGGTGAAGTGGAGAC CCTT C TOP1MT Ensembl:ENSG00000184428 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143328311..143331801 26863196 MeRIP-seq:(Medium) rs747979559 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4998308,Human_RBP_ID_22688545,Human_RBP_ID_26359413,Human_RBP_ID_27832189 Human_Splice_Rec_1018668,Human_Splice_Rec_1018698,Human_Splice_Rec_1018724,Human_Splice_Rec_1018752,Human_Splice_Rec_1018778,Human_Splice_Rec_1018796,Human_Splice_Rec_1018814,Human_Splice_Rec_1018828,Human_Splice_Rec_1018846,Human_Splice_Rec_1018858,Human_Splice_Rec_1018870,Human_Splice_Rec_1018880,Human_Splice_Rec_1018888 RMVar_hsa_circ_64222,RMVar_hsa_circ_59190 64614 RMVar_ID_64614 Human_SNP_ID_385924800 m1A Human chr8 - 143331332 143331329 143331332 TGACACGTCCTGTCTCCGTCTTTAGGTGGGAGAAGGAGAAGCACGAAGACGGGGTGAAGTGGAGA TGACACGTCCTGTCTCCGTCTTTAGGTGGGAG___GAGAAGCACGAAGACGGGGTGAAGTGGAGA CCTT C TOP1MT Ensembl:ENSG00000184428 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143331247..143331801 26863196 MeRIP-seq:(Medium) rs747979559 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4998308,Human_RBP_ID_22688545,Human_RBP_ID_27832189 Human_Splice_Rec_1018668,Human_Splice_Rec_1018698,Human_Splice_Rec_1018724,Human_Splice_Rec_1018752,Human_Splice_Rec_1018778,Human_Splice_Rec_1018796,Human_Splice_Rec_1018814,Human_Splice_Rec_1018828,Human_Splice_Rec_1018846,Human_Splice_Rec_1018858,Human_Splice_Rec_1018870,Human_Splice_Rec_1018880,Human_Splice_Rec_1018888 RMVar_hsa_circ_64222,RMVar_hsa_circ_59190 64615 RMVar_ID_64615 Human_SNP_ID_385935544 m1A Human chr8 + 143368927 143368927 143368927 AGGTGGTGCGGGCGGCCCTAGCCCGGCTGCGGAGCGCTGCGCGAGCGGCGGGCTGGCTGACCCCG AGGTGGTGCGGGCGGCCCTAGCCCGGCTGCGGGGCGCTGCGCGAGCGGCGGGCTGGCTGACCCCG A G RHPN1 Ensembl:ENSG00000158106 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143368878..143375640 26863196 MeRIP-seq:(Medium) rs1397327009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75779,RMVar_hsa_circ_254892 64616 RMVar_ID_64616 Human_SNP_ID_385938852 m1A Human chr8 + 143378380 143378376 143378381 TGTGTGGTTCCCCCGCCCACCCACCCTCCTGCAGCCCTGGGAGACACATGCGGAGGCTGAAGCTG TGTGTGGTTCCCCCGCCCACCCACCCTCC_____CCCTGGGAGACACATGCGGAGGCTGAAGCTG CTGCAG C RHPN1 Ensembl:ENSG00000158106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143378331..143378464 26863196 MeRIP-seq:(Medium) rs772006396 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_75779,RMVar_hsa_circ_109767,RMVar_hsa_circ_92846,RMVar_hsa_circ_254892,RMVar_hsa_circ_254893,RMVar_hsa_circ_254894 64617 RMVar_ID_64617 Human_SNP_ID_385938856 m1A Human chr8 + 143378380 143378379 143378381 TGTGTGGTTCCCCCGCCCACCCACCCTCCTGCAGCCCTGGGAGACACATGCGGAGGCTGAAGCTG TGTGTGGTTCCCCCGCCCACCCACCCTCCTGC__CCCTGGGAGACACATGCGGAGGCTGAAGCTG CAG C RHPN1 Ensembl:ENSG00000158106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143378331..143378464 26863196 MeRIP-seq:(Medium) rs777486816 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_75779,RMVar_hsa_circ_109767,RMVar_hsa_circ_92846,RMVar_hsa_circ_254892,RMVar_hsa_circ_254893,RMVar_hsa_circ_254894 64618 RMVar_ID_64618 Human_SNP_ID_385938857 m1A Human chr8 + 143378380 143378380 143378380 TGTGTGGTTCCCCCGCCCACCCACCCTCCTGCAGCCCTGGGAGACACATGCGGAGGCTGAAGCTG TGTGTGGTTCCCCCGCCCACCCACCCTCCTGCCGCCCTGGGAGACACATGCGGAGGCTGAAGCTG A C RHPN1 Ensembl:ENSG00000158106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143378331..143378464 26863196 MeRIP-seq:(Medium) rs773377826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75779,RMVar_hsa_circ_109767,RMVar_hsa_circ_92846,RMVar_hsa_circ_254892,RMVar_hsa_circ_254893,RMVar_hsa_circ_254894 64619 RMVar_ID_64619 Human_SNP_ID_385938901 m1A Human chr8 + 143378464 143378464 143378464 GAGCTCAGCGTAGACATCTCGAGGACGTGGGGAGACGGGCGCACCAGGGGCCCTGTGTGTCCAGA GAGCTCAGCGTAGACATCTCGAGGACGTGGGGGGACGGGCGCACCAGGGGCCCTGTGTGTCCAGA A G RHPN1 Ensembl:ENSG00000158106 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143378422..143378523 26863196 MeRIP-seq:(Medium) rs910402099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88812,Human_RBP_ID_844999,Human_RBP_ID_3973374,Human_RBP_ID_19022205,Human_RBP_ID_19140399,Human_RBP_ID_21994890,Human_RBP_ID_27831602 RMVar_hsa_circ_75779,RMVar_hsa_circ_109767,RMVar_hsa_circ_92846,RMVar_hsa_circ_254892,RMVar_hsa_circ_254893,RMVar_hsa_circ_254894 64620 RMVar_ID_64620 Human_SNP_ID_385948788 m1A Human chr8 + 143409092 143409092 143409092 GATTTGGGACCATCAAAGTTGGGGGTCAGGCCAGGGGTGGGAGGAGGGGCAGGGCCTGGGGGCCC GATTTGGGACCATCAAAGTTGGGGGTCAGGCCGGGGGTGGGAGGAGGGGCAGGGCCTGGGGGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143409072..143409176 26863196 MeRIP-seq:(Medium) rs1171469582 Functional Loss SNV dbSNP153 33..33 33 - - - 64621 RMVar_ID_64621 Human_SNP_ID_385950045 m1A Human chr8 + 143413242 143413242 143413242 AAGACCACTGCCACCCTCTGCCACCCTCCACCACCCTCCGCCAGGTCACCAGAATGCCAGGCCTC AAGACCACTGCCACCCTCTGCCACCCTCCACCTCCCTCCGCCAGGTCACCAGAATGCCAGGCCTC A T AC105118.1 Ensembl:ENSG00000253931 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143413239..143413369 26863196 MeRIP-seq:(Medium) rs1231554288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1018972 64622 RMVar_ID_64622 Human_SNP_ID_385950053 m1A Human chr8 - 143413283 143413283 143413283 GCTCTTCTCACCTGCCTGCTGGTGCTCAGCTGATCATGAGTGAGGCCTGGCATTCTGGTGACCTG GCTCTTCTCACCTGCCTGCTGGTGCTCAGCTGGTCATGAGTGAGGCCTGGCATTCTGGTGACCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143413234..143413318 26863196 MeRIP-seq:(Medium) rs765984792 Functional Loss SNV dbSNP153 33..33 33 - - - 64623 RMVar_ID_64623 Human_SNP_ID_385951700 m1A Human chr8 + 143418799 143418796 143418799 TGTTCACCCATCTACACACCATTTATTCACCCACCATCAACCATCCATATATCCTTCCATCCAGC TGTTCACCCATCTACACACCATTTATTCAC___CCATCAACCATCCATATATCCTTCCATCCAGC CCCA C MAFA-AS1 Ensembl:ENSG00000254338 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143418796..143418973 26863196 MeRIP-seq:(Medium) rs1394649159 Functional Loss DEL dbSNP153 31..33 33 - - - 64624 RMVar_ID_64624 Human_SNP_ID_385955663 m1A Human chr8 + 143430547 143430547 143430547 CGGGGGGGCGCCGGCGCGGGGCGGCGGCGCCGAGGGGCGCAGGGAAAAGTTTCACGTGGTCAACT CGGGGGGGCGCCGGCGCGGGGCGGCGGCGCCGGGGGGCGCAGGGAAAAGTTTCACGTGGTCAACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143430543..143430714 26863196 MeRIP-seq:(Medium) rs1389282079 Functional Loss SNV dbSNP153 33..33 33 - - - 64625 RMVar_ID_64625 Human_SNP_ID_385955745 m1A Human chr8 - 143430687 143430687 143430687 GGGGCCGGCCGGCGGCGCGGGTGGGGCGCGGGAGCGGTCCCGGAGCAGCCCGAGGCGGCGGCCGC GGGGCCGGCCGGCGGCGCGGGTGGGGCGCGGGGGCGGTCCCGGAGCAGCCCGAGGCGGCGGCCGC T C MAFA Ensembl:ENSG00000182759 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143430535..143430712 26863196 MeRIP-seq:(Medium) rs4486223 Functional Loss SNV dbSNP153 33..33 33 - - - 64626 RMVar_ID_64626 Human_SNP_ID_385971714 m1A Human chr8 + 143486675 143486675 143486675 AGAATGGCACCCGCTACATGACCCCACCACCAAGAAGCTCACACACAAAACAGCACCTGCTCCAC AGAATGGCACCCGCTACATGACCCCACCACCACGAAGCTCACACACAAAACAGCACCTGCTCCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143486673..143486838 26863196 MeRIP-seq:(Medium) rs1364765799 Functional Loss SNV dbSNP153 33..33 33 - - - 64627 RMVar_ID_64627 Human_SNP_ID_385973459 m1A Human chr8 - 143493243 143493243 143493243 GCCCTTGCTGGCAGGCAGGGCAGATCTGGGCCAGGACACAGGACCCTGAGGAGGGAGCCCCTGGG GCCCTTGCTGGCAGGCAGGGCAGATCTGGGCCGGGACACAGGACCCTGAGGAGGGAGCCCCTGGG T C ZC3H3 Ensembl:ENSG00000014164 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143493195..143493339 26863196 MeRIP-seq:(Medium) rs1033111584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90567,RMVar_hsa_circ_254896,RMVar_hsa_circ_337760,RMVar_hsa_circ_19981,RMVar_hsa_circ_88387,RMVar_hsa_circ_254901 64628 RMVar_ID_64628 Human_SNP_ID_385974960 m1A Human chr8 + 143498735 143498735 143498735 GCAGAGGGGTACAGGGCGGGGCGGAGGGGCACAGGGCGGGGCGGAGGGGTACAGGGCGGGGCGGA GCAGAGGGGTACAGGGCGGGGCGGAGGGGCACGGGGCGGGGCGGAGGGGTACAGGGCGGGGCGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143498734..143498809 26863196 MeRIP-seq:(Medium) rs1563861943 Functional Loss SNV dbSNP153 33..33 33 - - - 64629 RMVar_ID_64629 Human_SNP_ID_385986835 m1A Human chr8 - 143538748 143538748 143538748 CTGGTAAGCCCAGGATGGTGAAGTCAGTGGGCAGTGTGGGCGACAGCCCCCGGGAGCCCCGCCGG CTGGTAAGCCCAGGATGGTGAAGTCAGTGGGCGGTGTGGGCGACAGCCCCCGGGAGCCCCGCCGG T C ZC3H3 Ensembl:ENSG00000014164 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143538701..143538950 32194978 MeRIP-seq:(Medium) rs1162072106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959466,Human_RBP_ID_8923237,Human_RBP_ID_9313624 RMVar_hsa_circ_21607,RMVar_hsa_circ_254902,RMVar_hsa_circ_92082,RMVar_hsa_circ_24026 64630 RMVar_ID_64630 Human_SNP_ID_385987019 m1A Human chr8 - 143539098 143539098 143539098 GCCCCCGGGACCCTCAGACCCTCCTGCCGACCATGCTGTGCGGCCGTTGCACGGGGCCCGGGGGG GCCCCCGGGACCCTCAGACCCTCCTGCCGACCGTGCTGTGCGGCCGTTGCACGGGGCCCGGGGGG T C ZC3H3 Ensembl:ENSG00000014164 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143539049..143539149 32194978 MeRIP-seq:(Medium) rs200402267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21607,RMVar_hsa_circ_254902,RMVar_hsa_circ_92082,RMVar_hsa_circ_24026 64631 RMVar_ID_64631 Human_SNP_ID_385993904 m1A Human chr8 - 143560749 143560749 143560749 GGCTACACACCTGCAAGCACGTGGCTCCGGGCAGGGAAAACCGGCCCGAGCCCTCCCGCTTGTGG GGCTACACACCTGCAAGCACGTGGCTCCGGGCGGGGAAAACCGGCCCGAGCCCTCCCGCTTGTGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143560132..143560750 32194978 MeRIP-seq:(Medium) rs1387084519 Functional Loss SNV dbSNP153 33..33 33 - - - 64632 RMVar_ID_64632 Human_SNP_ID_385996054 m1A Human chr8 - 143566327 143566327 143566327 CTCCTCAGAGAAGCCTCTGCGAGTGCACAGGGAGTGTGTGCAGCCTTGTGAAGGGCTGGGACCAC CTCCTCAGAGAAGCCTCTGCGAGTGCACAGGGTGTGTGTGCAGCCTTGTGAAGGGCTGGGACCAC T A MROH6 Ensembl:ENSG00000204839 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143566278..143566399 32194978 MeRIP-seq:(Medium) rs918830348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1693735,Human_RBP_ID_2053285 64633 RMVar_ID_64633 Human_SNP_ID_385997665 m1A Human chr8 + 143569791 143569791 143569791 CGGGGTCTCCCTGCCAGGTGAGGAGTCGCTCCAGGATGACCTCCTCCCGCAGGAGCCGTGCGGTG CGGGGTCTCCCTGCCAGGTGAGGAGTCGCTCCGGGATGACCTCCTCCCGCAGGAGCCGTGCGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143568757..143569966 26863196 MeRIP-seq:(Medium) rs1376077734 Functional Loss SNV dbSNP153 33..33 33 - - - 64634 RMVar_ID_64634 Human_SNP_ID_385999543 m1A Human chr8 + 143573785 143573785 143573785 TGGTGTGTTCTGTCCAATGTGTGTGAGTCTGTATCTCTCTCCTAGCTCGTACTCCCCGGGGCTGG TGGTGTGTTCTGTCCAATGTGTGTGAGTCTGTTTCTCTCTCCTAGCTCGTACTCCCCGGGGCTGG A T AC067930.4 Ensembl:ENSG00000255050 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143573774..143574061 26863196 MeRIP-seq:(Medium) rs1271975383 Functional Loss SNV dbSNP153 33..33 33 - - - 64635 RMVar_ID_64635 Human_SNP_ID_386001045 m1A Human chr8 + 143577102 143577102 143577102 GGGGCACCTCGCTGCCTGAAAAGGAAGTGACGAAGGAGTGGGCCAGGGTCCCGGCCACCGGCACA GGGGCACCTCGCTGCCTGAAAAGGAAGTGACGGAGGAGTGGGCCAGGGTCCCGGCCACCGGCACA A G AC067930.4 Ensembl:ENSG00000255050 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143577051..143577151 32194978 MeRIP-seq:(Medium) rs749300189 Functional Loss SNV dbSNP153 33..33 33 - - - 64636 RMVar_ID_64636 Human_SNP_ID_386001173 m1A Human chr8 - 143577316 143577316 143577316 GCGGCTGCTAGAGATGGGCCTGAGGCGGGCTCAGGGCCCCGATGGGGGCCTGACAGCCTCCACCT GCGGCTGCTAGAGATGGGCCTGAGGCGGGCTCGGGGCCCCGATGGGGGCCTGACAGCCTCCACCT T C NAPRT Ensembl:ENSG00000147813 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143577046..143577334 26863196 MeRIP-seq:(Medium) rs1193595804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1019290,Human_Splice_Rec_1019291,Human_Splice_Rec_1019314,Human_Splice_Rec_1019315,Human_Splice_Rec_1019350,Human_Splice_Rec_1019351,Human_Splice_Rec_1019372,Human_Splice_Rec_1019373,Human_Splice_Rec_1019396,Human_Splice_Rec_1019397,Human_Splice_Rec_1019408,Human_Splice_Rec_1019409,Human_Splice_Rec_1019424,Human_Splice_Rec_1019425,Human_Splice_Rec_1019438,Human_Splice_Rec_1019446,Human_Splice_Rec_1019447,Human_Splice_Rec_1019452 RMVar_hsa_circ_89641,RMVar_hsa_circ_254908 64637 RMVar_ID_64637 Human_SNP_ID_386001375 m1A Human chr8 + 143577721 143577721 143577721 CTCCAGCAGCTGCACCACCAGGAGCGGCCCGGACACCTGCAGGAGCGGCACCTGCGGGGAGAGAA CTCCAGCAGCTGCACCACCAGGAGCGGCCCGGCCACCTGCAGGAGCGGCACCTGCGGGGAGAGAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143577249..143577954 32194978 MeRIP-seq:(Medium) rs376323296 Functional Loss SNV dbSNP153 33..33 33 - - - 64638 RMVar_ID_64638 Human_SNP_ID_386001715 m1A Human chr8 - 143578302 143578293 143578302 GGACGTCGGGAGCAGGATGGCGGCGGAGCAGGACCCCGAGGCGCGCGCGGCGGCGCGGCCGCTGC GGACGTCGGGAGCAGGATGGCGGCGGAGCAGG_________CGCGCGCGGCGGCGCGGCCGCTGC GCCTCGGGGT G NAPRT Ensembl:ENSG00000147813 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143577726..143578350;chr8:143577971..143578350 26863196 MeRIP-seq:(Medium) rs1563937432 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4995768,Human_RBP_ID_24555306 64639 RMVar_ID_64639 Human_SNP_ID_386001881 m1A Human chr8 - 143578608 143578608 143578608 TGCACCTCATTGCCCGGCCAAAGGGCAGAGACACGAGCGACTGGGGGCACCTCTGGTGACCAAGA TGCACCTCATTGCCCGGCCAAAGGGCAGAGACGCGAGCGACTGGGGGCACCTCTGGTGACCAAGA T C NAPRT Ensembl:ENSG00000147813 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143578457..143578608 26863196 MeRIP-seq:(Medium) rs1224352519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16378482 Human_Splice_Rec_1019441 64640 RMVar_ID_64640 Human_SNP_ID_386002256 m1A Human chr8 + 143579777 143579776 143579778 ATCGTGGCAGGGCCTCACGCACGCGCGCACGTACACACACTCAGGCTTCAGATCTTGTTGAAAGC ATCGTGGCAGGGCCTCACGCACGCGCGCACGT__ACACACTCAGGCTTCAGATCTTGTTGAAAGC TAC T AC067930.5,AC067930.1 Ensembl:ENSG00000279605,Ensembl:ENSG00000254741 Other,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143579726..143579850;chr8:143579726..143579857 26863196 MeRIP-seq:(Medium) rs1206066592 Functional Loss DEL dbSNP153 33..34 33 - - - 64641 RMVar_ID_64641 Human_SNP_ID_386002378 m1A Human chr8 - 143580037 143580037 143580037 GGACGACAAGGTGGGGACAGACTTGCTGGAGGAGGAGATCACCAAGTTTGAGGAGCACGTGAGTG GGACGACAAGGTGGGGACAGACTTGCTGGAGGTGGAGATCACCAAGTTTGAGGAGCACGTGAGTG T A EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr8:143580001..143580100;chr8:143579726..143580076 26863196,32194978 MeRIP-seq:(Medium) rs760177855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695498,Human_RBP_ID_795483,Human_RBP_ID_3874610,Human_RBP_ID_5123666,Human_RBP_ID_9338767,Human_RBP_ID_9405847,Human_RBP_ID_17666027,Human_RBP_ID_18893078 Human_Splice_Rec_1019467,Human_Splice_Rec_1019483,Human_Splice_Rec_1019497,Human_Splice_Rec_1019501,Human_Splice_Rec_1019505,Human_Splice_Rec_1019509,Human_Splice_Rec_1019515,Human_Splice_Rec_1019529,Human_Splice_Rec_1019543,Human_Splice_Rec_1019561,Human_Splice_Rec_1019573,Human_Splice_Rec_1019585,Human_Splice_Rec_1019599,Human_Splice_Rec_1019613,Human_Splice_Rec_1019627,Human_Splice_Rec_1019639,Human_Splice_Rec_1019653 Human_miRNA_ID_1103690 RMVar_hsa_circ_377557,RMVar_hsa_circ_254909 64642 RMVar_ID_64642 Human_SNP_ID_386002381 m1A Human chr8 + 143580058 143580058 143580058 TGGTGATCTCCTCCTCCAGCAAGTCTGTCCCCACCTTGTCGTCCTCCACCACACACTGAATCTGT TGGTGATCTCCTCCTCCAGCAAGTCTGTCCCCTCCTTGTCGTCCTCCACCACACACTGAATCTGT A T AC067930.5,AC067930.1 Ensembl:ENSG00000279605,Ensembl:ENSG00000254741 Other,lincRNA exon,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:143580012..143580147 26863196 MeRIP-seq:(Medium) rs1062401 Functional Loss SNV dbSNP153 33..33 33 - - - 64643 RMVar_ID_64643 Human_SNP_ID_386002593 m1A Human chr8 - 143580561 143580559 143580562 GGAGGAGCGGCTACGGCAGTACGCGGAGAAGAAGGCCAAGAAGCCTGCACTGGTGGCCAAGTCCT GGAGGAGCGGCTACGGCAGTACGCGGAGAAG___GCCAAGAAGCCTGCACTGGTGGCCAAGTCCT CCTT C EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143580480..143580751 26863196 MeRIP-seq:(Medium) rs756390399 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5123667,Human_RBP_ID_5153944,Human_RBP_ID_9405848,Human_RBP_ID_18125345,Human_RBP_ID_18196776,Human_RBP_ID_19022227,Human_RBP_ID_22465312 Human_Splice_Rec_1019465,Human_Splice_Rec_1019481,Human_Splice_Rec_1019495,Human_Splice_Rec_1019503,Human_Splice_Rec_1019507,Human_Splice_Rec_1019513,Human_Splice_Rec_1019527,Human_Splice_Rec_1019541,Human_Splice_Rec_1019559,Human_Splice_Rec_1019571,Human_Splice_Rec_1019582,Human_Splice_Rec_1019583,Human_Splice_Rec_1019597,Human_Splice_Rec_1019611,Human_Splice_Rec_1019624,Human_Splice_Rec_1019625,Human_Splice_Rec_1019637,Human_Splice_Rec_1019651,Human_Splice_Rec_1019666,Human_Splice_Rec_1019667,Human_Splice_Rec_1019683,Human_Splice_Rec_1019697,Human_Splice_Rec_1019700,Human_Splice_Rec_1019701,Human_Splice_Rec_1019711,Human_Splice_Rec_1019756 Human_miRNA_ID_1348976,Human_miRNA_ID_1812776,Human_miRNA_ID_2078472,Human_miRNA_ID_2080789,Human_miRNA_ID_2091336 RMVar_hsa_circ_94071,RMVar_hsa_circ_377557,RMVar_hsa_circ_254909,RMVar_hsa_circ_254910 64644 RMVar_ID_64644 Human_SNP_ID_386002594 m1A Human chr8 - 143580561 143580561 143580561 GGAGGAGCGGCTACGGCAGTACGCGGAGAAGAAGGCCAAGAAGCCTGCACTGGTGGCCAAGTCCT GGAGGAGCGGCTACGGCAGTACGCGGAGAAGACGGCCAAGAAGCCTGCACTGGTGGCCAAGTCCT T G EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143580480..143580751 26863196 MeRIP-seq:(Medium) rs761160836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123667,Human_RBP_ID_5153944,Human_RBP_ID_9405848,Human_RBP_ID_18125345,Human_RBP_ID_18196776,Human_RBP_ID_19022227,Human_RBP_ID_22465312 Human_Splice_Rec_1019465,Human_Splice_Rec_1019481,Human_Splice_Rec_1019495,Human_Splice_Rec_1019503,Human_Splice_Rec_1019507,Human_Splice_Rec_1019513,Human_Splice_Rec_1019527,Human_Splice_Rec_1019541,Human_Splice_Rec_1019559,Human_Splice_Rec_1019571,Human_Splice_Rec_1019582,Human_Splice_Rec_1019583,Human_Splice_Rec_1019597,Human_Splice_Rec_1019611,Human_Splice_Rec_1019624,Human_Splice_Rec_1019625,Human_Splice_Rec_1019637,Human_Splice_Rec_1019651,Human_Splice_Rec_1019666,Human_Splice_Rec_1019667,Human_Splice_Rec_1019683,Human_Splice_Rec_1019697,Human_Splice_Rec_1019700,Human_Splice_Rec_1019701,Human_Splice_Rec_1019711,Human_Splice_Rec_1019756 Human_miRNA_ID_1348976,Human_miRNA_ID_1812776,Human_miRNA_ID_2078472,Human_miRNA_ID_2080789,Human_miRNA_ID_2091336 RMVar_hsa_circ_94071,RMVar_hsa_circ_377557,RMVar_hsa_circ_254909,RMVar_hsa_circ_254910 64645 RMVar_ID_64645 Human_SNP_ID_386002810 m1A Human chr8 + 143581033 143581033 143581033 GCCAGCAGGGCCACGTGGTCCCCTGCAGTGTCAGGCGTGGGGAGAGCATTCACCTGGGTCTGTGG GCCAGCAGGGCCACGTGGTCCCCTGCAGTGTCCGGCGTGGGGAGAGCATTCACCTGGGTCTGTGG A C AC067930.5 Ensembl:ENSG00000279605 Other exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143581031..143581245 26863196 MeRIP-seq:(Medium) rs1163302689 Functional Loss SNV dbSNP153 33..33 33 - - - 64646 RMVar_ID_64646 Human_SNP_ID_386004431 m1A Human chr8 - 143586286 143586286 143586286 AGACTGGTTCTTTCTGCACTGTCTGCAGGAGAACGGCGCCAGCGTGATCCTCCGTGACATTGCGA AGACTGGTTCTTTCTGCACTGTCTGCAGGAGAGCGGCGCCAGCGTGATCCTCCGTGACATTGCGA T C EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:143586194..143586323;chr8:143586251..143586300 26863196 MeRIP-seq:(Medium) rs1240044926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795488,Human_RBP_ID_961052,Human_RBP_ID_16378775,Human_RBP_ID_18196572,Human_RBP_ID_19023146 Human_Splice_Rec_1019458,Human_Splice_Rec_1019459,Human_Splice_Rec_1019474,Human_Splice_Rec_1019475,Human_Splice_Rec_1019488,Human_Splice_Rec_1019489,Human_Splice_Rec_1019520,Human_Splice_Rec_1019521,Human_Splice_Rec_1019534,Human_Splice_Rec_1019535,Human_Splice_Rec_1019552,Human_Splice_Rec_1019553,Human_Splice_Rec_1019590,Human_Splice_Rec_1019591,Human_Splice_Rec_1019604,Human_Splice_Rec_1019605,Human_Splice_Rec_1019618,Human_Splice_Rec_1019619,Human_Splice_Rec_1019660,Human_Splice_Rec_1019661,Human_Splice_Rec_1019676,Human_Splice_Rec_1019677,Human_Splice_Rec_1019690,Human_Splice_Rec_1019691,Human_Splice_Rec_1019716,Human_Splice_Rec_1019717,Human_Splice_Rec_1019728,Human_Splice_Rec_1019729,Human_Splice_Rec_1019740,Human_Splice_Rec_1019741,Human_Splice_Rec_1019750,Human_Splice_Rec_1019751,Human_Splice_Rec_1019762,Human_Splice_Rec_1019763,Human_Splice_Rec_1019772,Human_Splice_Rec_1019773,Human_Splice_Rec_1019782,Human_Splice_Rec_1019783,Human_Splice_Rec_1019790,Human_Splice_Rec_1019791,Human_Splice_Rec_1019800,Human_Splice_Rec_1019801,Human_Splice_Rec_1019810,Human_Splice_Rec_1019811,Human_Splice_Rec_1019820,Human_Splice_Rec_1019821,Human_Splice_Rec_1019828,Human_Splice_Rec_1019838 RMVar_hsa_circ_94071,RMVar_hsa_circ_377557,RMVar_hsa_circ_254909,RMVar_hsa_circ_128073,RMVar_hsa_circ_254910,RMVar_hsa_circ_254912 64647 RMVar_ID_64647 Human_SNP_ID_386004647 m1A Human chr8 - 143586825 143586825 143586825 CCCAGCAGAAAAATGGCTACAAACTTCCTAGCACATGAGAAGATCTGGTTCGACAAGTTCAAATA CCCAGCAGAAAAATGGCTACAAACTTCCTAGCCCATGAGAAGATCTGGTTCGACAAGTTCAAATA T G EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr8:143586776..143586850 26863196 MeRIP-seq:(Medium) rs1273480349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2053315,Human_RBP_ID_16378779,Human_RBP_ID_18893116,Human_RBP_ID_22689384,Human_RBP_ID_27121754 Human_Splice_Rec_1019456,Human_Splice_Rec_1019457,Human_Splice_Rec_1019472,Human_Splice_Rec_1019473,Human_Splice_Rec_1019486,Human_Splice_Rec_1019487,Human_Splice_Rec_1019500,Human_Splice_Rec_1019518,Human_Splice_Rec_1019519,Human_Splice_Rec_1019532,Human_Splice_Rec_1019533,Human_Splice_Rec_1019550,Human_Splice_Rec_1019551,Human_Splice_Rec_1019564,Human_Splice_Rec_1019565,Human_Splice_Rec_1019576,Human_Splice_Rec_1019577,Human_Splice_Rec_1019588,Human_Splice_Rec_1019589,Human_Splice_Rec_1019602,Human_Splice_Rec_1019603,Human_Splice_Rec_1019616,Human_Splice_Rec_1019617,Human_Splice_Rec_1019630,Human_Splice_Rec_1019631,Human_Splice_Rec_1019644,Human_Splice_Rec_1019645,Human_Splice_Rec_1019658,Human_Splice_Rec_1019659,Human_Splice_Rec_1019674,Human_Splice_Rec_1019675,Human_Splice_Rec_1019688,Human_Splice_Rec_1019689,Human_Splice_Rec_1019699,Human_Splice_Rec_1019704,Human_Splice_Rec_1019705,Human_Splice_Rec_1019714,Human_Splice_Rec_1019715,Human_Splice_Rec_1019726,Human_Splice_Rec_1019727,Human_Splice_Rec_1019738,Human_Splice_Rec_1019739,Human_Splice_Rec_1019748,Human_Splice_Rec_1019749,Human_Splice_Rec_1019760,Human_Splice_Rec_1019761,Human_Splice_Rec_1019770,Human_Splice_Rec_1019771,Human_Splice_Rec_1019780,Human_Splice_Rec_1019781,Human_Splice_Rec_1019789,Human_Splice_Rec_1019798,Human_Splice_Rec_1019799,Human_Splice_Rec_1019808,Human_Splice_Rec_1019809,Human_Splice_Rec_1019818,Human_Splice_Rec_1019819,Human_Splice_Rec_1019826,Human_Splice_Rec_1019827,Human_Splice_Rec_1019836,Human_Splice_Rec_1019837,Human_Splice_Rec_1019840,Human_Splice_Rec_1019842 RMVar_hsa_circ_94071,RMVar_hsa_circ_377557,RMVar_hsa_circ_254909,RMVar_hsa_circ_128073,RMVar_hsa_circ_254910,RMVar_hsa_circ_254912 64648 RMVar_ID_64648 Human_SNP_ID_386004963 m1A Human chr8 - 143587738 143587738 143587738 GTAAAACCACAGGCTGGATTTGCCTGCGGGCCATGGTCCCTGTCTAGGGCAGCAATTCTCAACCT GTAAAACCACAGGCTGGATTTGCCTGCGGGCCGTGGTCCCTGTCTAGGGCAGCAATTCTCAACCT T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143587736..143588029 26863196 MeRIP-seq:(Medium) rs1423650314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16378821,Human_RBP_ID_22836394,Human_RBP_ID_24249611 64649 RMVar_ID_64649 Human_SNP_ID_386005046 m1A Human chr8 + 143588057 143588057 143588057 GAGTCTGTGAGCGTCCTCTGCGTCCCTGACCCAGGACACTCTCTCGGCAAGGAGGGACCAGGCCA GAGTCTGTGAGCGTCCTCTGCGTCCCTGACCCGGGACACTCTCTCGGCAAGGAGGGACCAGGCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143588051..143588075 26863196 MeRIP-seq:(Medium) rs559559978 Functional Loss SNV dbSNP153 33..33 33 - - - 64650 RMVar_ID_64650 Human_SNP_ID_386005094 m1A Human chr8 - 143588240 143588240 143588240 GTGGGGCGGGCTGAGTCAGGGAAGGACTCTGAAGGTCCCAAGCAGCTGCTGAGGCCCCCAAGGAA GTGGGGCGGGCTGAGTCAGGGAAGGACTCTGATGGTCCCAAGCAGCTGCTGAGGCCCCCAAGGAA T A EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143588236..143588435 26863196 MeRIP-seq:(Medium) rs1320521193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89694,Human_RBP_ID_268220,Human_RBP_ID_1070405,Human_RBP_ID_3885533,Human_RBP_ID_5123534,Human_RBP_ID_5224226,Human_RBP_ID_5406792,Human_RBP_ID_8155033,Human_RBP_ID_8221522,Human_RBP_ID_8731013,Human_RBP_ID_9441019,Human_RBP_ID_16378868,Human_RBP_ID_18172482,Human_RBP_ID_18467174,Human_RBP_ID_18961238,Human_RBP_ID_19142561,Human_RBP_ID_22372517,Human_RBP_ID_22731668,Human_RBP_ID_22836404,Human_RBP_ID_23083976,Human_RBP_ID_24249614,Human_RBP_ID_26795701,Human_RBP_ID_27121786,Human_RBP_ID_27574617,Human_RBP_ID_27843351 64651 RMVar_ID_64651 Human_SNP_ID_386005174 m1A Human chr8 - 143588543 143588543 143588543 AGCCAGTGTGTCCCTGCCTGTCCATCCTGTGCACCCCCAGCTTTCCTTGTCACCTGAAACCACCT AGCCAGTGTGTCCCTGCCTGTCCATCCTGTGCGCCCCCAGCTTTCCTTGTCACCTGAAACCACCT T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143588540..143588606 26863196 MeRIP-seq:(Medium) rs968531726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1335089,Human_RBP_ID_3885534,Human_RBP_ID_5224530,Human_RBP_ID_18506465,Human_RBP_ID_22329175,Human_RBP_ID_22836409,Human_RBP_ID_23299333,Human_RBP_ID_27121792,Human_RBP_ID_27363385 64652 RMVar_ID_64652 Human_SNP_ID_386005411 m1A Human chr8 + 143589149 143589149 143589149 TAGGCAGGCTTGCTGAGCCAGGGGGCCTCTGCATCCTTCTGCAGGAAGTAACAGTAGGGCAAGGC TAGGCAGGCTTGCTGAGCCAGGGGGCCTCTGCGTCCTTCTGCAGGAAGTAACAGTAGGGCAAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143588895..143590095 32194978 MeRIP-seq:(Medium) rs369512896 Functional Loss SNV dbSNP153 33..33 33 - - - 64653 RMVar_ID_64653 Human_SNP_ID_386005555 m1A Human chr8 + 143589381 143589381 143589381 CCCTCTCGGCTGCATCATACCGGGGCTTCTCCAGCCACACCTCCCGAACCAGTGCCTGCAGGCTG CCCTCTCGGCTGCATCATACCGGGGCTTCTCCGGCCACACCTCCCGAACCAGTGCCTGCAGGCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143589376..143589425 26863196 MeRIP-seq:(Medium) rs575252015 Functional Loss SNV dbSNP153 33..33 33 - - - 64654 RMVar_ID_64654 Human_SNP_ID_386005575 m1A Human chr8 + 143589435 143589435 143589435 CCTGCAGGCTGCCCAGCGGGGGCTGGCCATTGACCGGTGGGCTGGGCTGGTGGGCCAGGTCGGGG CCTGCAGGCTGCCCAGCGGGGGCTGGCCATTGGCCGGTGGGCTGGGCTGGTGGGCCAGGTCGGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143589432..143589520 26863196 MeRIP-seq:(Medium) rs921884165 Functional Loss SNV dbSNP153 33..33 33 - - - 64655 RMVar_ID_64655 Human_SNP_ID_386005830 m1A Human chr8 + 143589957 143589945 143589957 CGGGCCCATTCATGGCTGGCCCCTCGGCTGGCAGCTGCTGGGCGGAGGCGGCCGCCTGTGTGGCC CGGGCCCATTCATGGCTGGCC____________GCTGCTGGGCGGAGGCGGCCGCCTGTGTGGCC CCCTCGGCTGGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:143589955..143590195;chr8:143589951..143590109 26863196 MeRIP-seq:(Medium) rs1161904904 Functional Loss DEL dbSNP153 22..33 33 - - - 64656 RMVar_ID_64656 Human_SNP_ID_386006162 m1A Human chr8 + 143590886 143590886 143590886 CCGAGATGGCGCCACTGCACTCCAGCCTGGACAACAGAGCAGGGGAAAAGAAAAAAAAAGAGGGA CCGAGATGGCGCCACTGCACTCCAGCCTGGACCACAGAGCAGGGGAAAAGAAAAAAAAAGAGGGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143590876..143590950 26863196 MeRIP-seq:(Medium) rs961888805 Functional Loss SNV dbSNP153 33..33 33 - - - 64657 RMVar_ID_64657 Human_SNP_ID_386006744 m1A Human chr8 + 143593132 143593132 143593132 CCCCTGTGTCCGGTCTGCTGAAGGAGGCCCGGAAGATGACAAGGACCCTCAAGGGGGAGGCAGCC CCCCTGTGTCCGGTCTGCTGAAGGAGGCCCGGCAGATGACAAGGACCCTCAAGGGGGAGGCAGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143593129..143593217 26863196 MeRIP-seq:(Medium) rs1354037866 Functional Loss SNV dbSNP153 33..33 33 - - - 64658 RMVar_ID_64658 Human_SNP_ID_386007478 m1A Human chr8 - 143595703 143595703 143595703 CTCAAGCAGGGCTGGCCATGGAGCTGGCCTGCAGTGGCATTTAAGAAAAGACGTGGTTGGGGCGG CTCAAGCAGGGCTGGCCATGGAGCTGGCCTGCTGTGGCATTTAAGAAAAGACGTGGTTGGGGCGG T A EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143595451..143595850;chr8:143595501..143595850 26863196 MeRIP-seq:(Medium) rs989788433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7817675,Human_RBP_ID_8682711,Human_RBP_ID_18893220,Human_RBP_ID_27774450 64659 RMVar_ID_64659 Human_SNP_ID_386007479 m1A Human chr8 - 143595703 143595703 143595703 CTCAAGCAGGGCTGGCCATGGAGCTGGCCTGCAGTGGCATTTAAGAAAAGACGTGGTTGGGGCGG CTCAAGCAGGGCTGGCCATGGAGCTGGCCTGCGGTGGCATTTAAGAAAAGACGTGGTTGGGGCGG T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143595451..143595850;chr8:143595501..143595850 26863196 MeRIP-seq:(Medium) rs989788433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7817675,Human_RBP_ID_8682711,Human_RBP_ID_18893220,Human_RBP_ID_27774450 64660 RMVar_ID_64660 Human_SNP_ID_386007958 m1A Human chr8 + 143597186 143597186 143597186 CCTCCGTCGCCCCGCCTCTCTGCGCTCGCCCCAAGTGCCGCACTTGGCCCACGGCCCCTAAGCCC CCTCCGTCGCCCCGCCTCTCTGCGCTCGCCCCGAGTGCCGCACTTGGCCCACGGCCCCTAAGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143597034..143597513 26863196 MeRIP-seq:(Medium) rs559597445 Functional Loss SNV dbSNP153 33..33 33 - - - 64661 RMVar_ID_64661 Human_SNP_ID_386007959 m1A Human chr8 + 143597186 143597186 143597186 CCTCCGTCGCCCCGCCTCTCTGCGCTCGCCCCAAGTGCCGCACTTGGCCCACGGCCCCTAAGCCC CCTCCGTCGCCCCGCCTCTCTGCGCTCGCCCCTAGTGCCGCACTTGGCCCACGGCCCCTAAGCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143597034..143597513 26863196 MeRIP-seq:(Medium) rs559597445 Functional Loss SNV dbSNP153 33..33 33 - - - 64662 RMVar_ID_64662 Human_SNP_ID_386008057 m1A Human chr8 + 143597409 143597409 143597409 GGAGGAATCGGCGGACGCGGGAAGACTGATGAAAGGGAGGGCCGCCCGGGCCGCGCACGGGAAAT GGAGGAATCGGCGGACGCGGGAAGACTGATGAGAGGGAGGGCCGCCCGGGCCGCGCACGGGAAAT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:143597334..143597470 26863410 MeRIP-seq:(Medium) rs193125775 Functional Loss SNV dbSNP153 33..33 33 - - - 64663 RMVar_ID_64663 Human_SNP_ID_386008329 m1A Human chr8 - 143597999 143597999 143597999 CGCGGCCCGGGCGCGGGGGGCGGCGGCCGTGCAGCGGGGACGGGGGCTGGGGCGGGCGCGGGGGG CGCGGCCCGGGCGCGGGGGGCGGCGGCCGTGCGGCGGGGACGGGGGCTGGGGCGGGCGCGGGGGG T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:143597900..143598012 26863410 MeRIP-seq:(Medium) rs1349203894 Functional Loss SNV dbSNP153 33..33 33 - - - 64664 RMVar_ID_64664 Human_SNP_ID_386008393 m1A Human chr8 - 143598144 143598144 143598144 CCAGCCGCGCAGCGTCCCGCCCGGCACGCCGAAGTCGCGGCACACACTGGCCTGCCGCTCGCCGC CCAGCCGCGCAGCGTCCCGCCCGGCACGCCGAGGTCGCGGCACACACTGGCCTGCCGCTCGCCGC T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143598093..143598253 26863196 MeRIP-seq:(Medium) rs1220537278 Functional Loss SNV dbSNP153 33..33 33 - - - 64665 RMVar_ID_64665 Human_SNP_ID_386011654 m1A Human chr8 - 143607134 143607134 143607134 CCCCTGAGGCTTGGTCCTGGTGTCCCTGGCGCAGGCTCTGGGTTGCCGGACCACGCACTCCAACC CCCCTGAGGCTTGGTCCTGGTGTCCCTGGCGCCGGCTCTGGGTTGCCGGACCACGCACTCCAACC T G PYCR3 Ensembl:ENSG00000104524 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143607124..143607347 26863196 MeRIP-seq:(Medium) rs1352448397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4973403,Human_RBP_ID_22329340,Human_RBP_ID_26766060 64666 RMVar_ID_64666 Human_SNP_ID_386012458 m1A Human chr8 - 143609535 143609535 143609535 CGGCGTCCGAGGCAACAAGATGGCAGCTGCGGAGCCGTCTCCGCGGCGCGTGGGCTTCGTGGGCG CGGCGTCCGAGGCAACAAGATGGCAGCTGCGGCGCCGTCTCCGCGGCGCGTGGGCTTCGTGGGCG T G PYCR3 Ensembl:ENSG00000104524 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143609417..143609575;chr8:143609451..143609553 26863196 MeRIP-seq:(Medium) rs768910534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995770,Human_RBP_ID_24249694 Human_Splice_Rec_1019913,Human_Splice_Rec_1019923,Human_Splice_Rec_1019933,Human_Splice_Rec_1019945,Human_Splice_Rec_1019973 64667 RMVar_ID_64667 Human_SNP_ID_386014001 m1A Human chr8 + 143613555 143613555 143613555 CGGTGACTTCCCCATGGAAGTCCATGGCCTCCACCACCGCCTCGGCTGCCTCCTTGATGGAGACC CGGTGACTTCCCCATGGAAGTCCATGGCCTCCGCCACCGCCTCGGCTGCCTCCTTGATGGAGACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143613176..143614634 32194978 MeRIP-seq:(Medium) rs1194177826 Functional Loss SNV dbSNP153 33..33 33 - - - 64668 RMVar_ID_64668 Human_SNP_ID_386014403 m1A Human chr8 - 143614455 143614455 143614455 CAGGACGAGGGCAGGAGACGCTGTGCCTCCGCAGGGCCTACTTCCAGCAGTACGGCTGCACCTTC CAGGACGAGGGCAGGAGACGCTGTGCCTCCGCCGGGCCTACTTCCAGCAGTACGGCTGCACCTTC T G TSTA3 Ensembl:ENSG00000104522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143614316..143614632;chr8:143614428..143614618 26863196 MeRIP-seq:(Medium) rs1261284188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958265,Human_RBP_ID_3973392,Human_RBP_ID_5405012,Human_RBP_ID_18172682,Human_RBP_ID_22555835,Human_RBP_ID_23259510,Human_RBP_ID_24391137 RMVar_hsa_circ_85140,RMVar_hsa_circ_254914 64669 RMVar_ID_64669 Human_SNP_ID_386019026 m1A Human chr8 - 143632258 143632258 143632258 GGTAGGGGTGGCCTGGAGGCAGGTCTCTTCTGAGTATCACAAAGCACATCCAAAAGTAAATGATG GGTAGGGGTGGCCTGGAGGCAGGTCTCTTCTGCGTATCACAAAGCACATCCAAAAGTAAATGATG T G AC067930.2 Ensembl:ENSG00000254812 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143632247..143632490 26863196 MeRIP-seq:(Medium) rs1162062910 Functional Loss SNV dbSNP153 33..33 33 - - - 64670 RMVar_ID_64670 Human_SNP_ID_386020220 m1A Human chr8 + 143636107 143636107 143636107 GCCCGCGCCGGCGGGGTCCAGTCAGCGGCTGCAGGGTCGGGCTCGCGCCGTCCTCTCCCCGCCCG GCCCGCGCCGGCGGGGTCCAGTCAGCGGCTGCGGGGTCGGGCTCGCGCCGTCCTCTCCCCGCCCG A G ZNF623 Ensembl:ENSG00000183309 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143636059..143636242 26863196 MeRIP-seq:(Medium) rs1200826457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995239,Human_RBP_ID_18426767,Human_RBP_ID_18505963,Human_RBP_ID_22372524 Human_Splice_Rec_1020119 64671 RMVar_ID_64671 Human_SNP_ID_386023492 m1A Human chr8 + 143647673 143647673 143647673 GAGGGCAGGGTGAGCAGCAGGAGTCCAGGCCCAGTGGCCCTTGTGGGGCCAGAGTAGGGGATGGG GAGGGCAGGGTGAGCAGCAGGAGTCCAGGCCCGGTGGCCCTTGTGGGGCCAGAGTAGGGGATGGG A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143647667..143648203 26863196 MeRIP-seq:(Medium) rs7827272 Functional Loss SNV dbSNP153 33..33 33 - - - 64672 RMVar_ID_64672 Human_SNP_ID_386034329 m1A Human chr8 + 143684516 143684516 143684516 AGTCTGGGCTACCGGCGCGGCGTAGTGGATGCAGCATCCTAGTGGAGGACGCCCCTGTGGTGAGT AGTCTGGGCTACCGGCGCGGCGTAGTGGATGCTGCATCCTAGTGGAGGACGCCCCTGTGGTGAGT A T ZNF707 Ensembl:ENSG00000181135 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143684513..143684596 26863196 MeRIP-seq:(Medium) rs62524205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1020123,Human_Splice_Rec_1020127,Human_Splice_Rec_1020135,Human_Splice_Rec_1020143,Human_Splice_Rec_1020151,Human_Splice_Rec_1020153,Human_Splice_Rec_1020163,Human_Splice_Rec_1020173,Human_Splice_Rec_1020181,Human_Splice_Rec_1020191,Human_Splice_Rec_1020201,Human_Splice_Rec_1020211,Human_Splice_Rec_1020217,Human_Splice_Rec_1020227,Human_Splice_Rec_1020235,Human_Splice_Rec_1020243,Human_Splice_Rec_1020251,Human_Splice_Rec_1020255,Human_Splice_Rec_1020261,Human_Splice_Rec_1020267,Human_Splice_Rec_1020279,Human_Splice_Rec_1020285,Human_Splice_Rec_1020297,Human_Splice_Rec_1020303,Human_Splice_Rec_1020315 64673 RMVar_ID_64673 Human_SNP_ID_386036115 m1A Human chr8 - 143691103 143691103 143691103 TTCCAGACACGCCCACTCCTCCCTTGAGAAGTAGATGGCCACGTCCCTGAAGGTCACTGGCTCCT TTCCAGACACGCCCACTCCTCCCTTGAGAAGTCGATGGCCACGTCCCTGAAGGTCACTGGCTCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143691094..143691182 26863196 MeRIP-seq:(Medium) rs782760703 Functional Loss SNV dbSNP153 33..33 33 - - - 64674 RMVar_ID_64674 Human_SNP_ID_386037375 m1A Human chr8 + 143694517 143694517 143694517 GTTCTTCACGCGGCATCAGAGGACTCACAGGCACGGGGAGGTGTAGGGGCGCCCGAAGAGTGGGG GTTCTTCACGCGGCATCAGAGGACTCACAGGCCCGGGGAGGTGTAGGGGCGCCCGAAGAGTGGGG A C ZNF707 Ensembl:ENSG00000181135 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143694467..143694644 26863196 MeRIP-seq:(Medium) rs1563733260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5514532 Human_miRNA_ID_2015747 RMVar_hsa_circ_254927,RMVar_hsa_circ_378815 64675 RMVar_ID_64675 Human_SNP_ID_386037716 m1A Human chr8 + 143695669 143695646 143695669 ATAGGGGGATGAGGAGAAGGTTGAACACACCGAGAGGAAGCCCTGAGCCAGATCCGGCTGGAGAT ATAGGGGGAT_______________________GAGGAAGCCCTGAGCCAGATCCGGCTGGAGAT TGAGGAGAAGGTTGAACACACCGA T ZNF707 Ensembl:ENSG00000181135 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143695665..143695822 26863196 MeRIP-seq:(Medium) rs1446283883 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_3885566,Human_RBP_ID_22732511 64676 RMVar_ID_64676 Human_SNP_ID_386037864 m1A Human chr8 - 143696146 143696146 143696146 ACAGCCCACCCACCCGACTCACGGCCACCCACACGACTCAGTCCATCCACCCGACTCACGGCCCA ACAGCCCACCCACCCGACTCACGGCCACCCACCCGACTCAGTCCATCCACCCGACTCACGGCCCA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143696131..143696377 26863196 MeRIP-seq:(Medium) rs61433887 Functional Loss SNV dbSNP153 33..33 33 - - - 64677 RMVar_ID_64677 Human_SNP_ID_386037883 m1A Human chr8 - 143696206 143696168 143696206 TCACGGCCCACCCACGCAACTCACGGCCCACCACGCAACTCACGGCCACCCACCCGACTCACAGC TCACGGCCCACCCACGCAACTCACGGCCCACC_________________________________ GGGTGGGCTGTGAGTCGGGTGGGTGGCCGTGAGTTGCGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143696110..143696350 26863196 MeRIP-seq:(Medium) rs1554615322 Functional Loss DEL dbSNP153 33..65 33 - - - 64678 RMVar_ID_64678 Human_SNP_ID_386037928 m1A Human chr8 - 143696216 143696216 143696216 CCCACCCGACTCACGGCCCACCCACGCAACTCACGGCCCACCACGCAACTCACGGCCACCCACCC CCCACCCGACTCACGGCCCACCCACGCAACTCCCGGCCCACCACGCAACTCACGGCCACCCACCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143696104..143696402;chr8:143696099..143696399;chr8:143696115..143696404 26863196 MeRIP-seq:(Medium) rs1554615339 Functional Loss SNV dbSNP153 33..33 33 - - - 64679 RMVar_ID_64679 Human_SNP_ID_386042749 m1A Human chr8 - 143711563 143711562 143711563 CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGGACGGGGAGGGCCTCACAGGGAGCAGACAGTGCC CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGG_CGGGGAGGGCCTCACAGGGAGCAGACAGTGCC GT G AC105219.2 Ensembl:ENSG00000254574 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143711560..143711684 26863196 MeRIP-seq:(Medium) rs1563743139 Functional Loss DEL dbSNP153 33..33 33 - - - 64680 RMVar_ID_64680 Human_SNP_ID_386042752 m1A Human chr8 - 143711563 143711563 143711563 CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGGACGGGGAGGGCCTCACAGGGAGCAGACAGTGCC CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGGTCGGGGAGGGCCTCACAGGGAGCAGACAGTGCC T A AC105219.2 Ensembl:ENSG00000254574 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143711560..143711684 26863196 MeRIP-seq:(Medium) rs13250597 Functional Loss SNV dbSNP153 33..33 33 - - - 64681 RMVar_ID_64681 Human_SNP_ID_386042753 m1A Human chr8 - 143711563 143711563 143711563 CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGGACGGGGAGGGCCTCACAGGGAGCAGACAGTGCC CGGTGAAAGGAGGGAGGCTGGCCCAGCTGTGGGCGGGGAGGGCCTCACAGGGAGCAGACAGTGCC T C AC105219.2 Ensembl:ENSG00000254574 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143711560..143711684 26863196 MeRIP-seq:(Medium) rs13250597 Functional Loss SNV dbSNP153 33..33 33 - - - 64682 RMVar_ID_64682 Human_SNP_ID_386042772 m1A Human chr8 + 143711592 143711592 143711592 CCGTCCACAGCTGGGCCAGCCTCCCTCCTTTCACCGCCCTCCCCACAGCCCCGAAGCCGGGCCAG CCGTCCACAGCTGGGCCAGCCTCCCTCCTTTCCCCGCCCTCCCCACAGCCCCGAAGCCGGGCCAG A C ZNF707 Ensembl:ENSG00000181135 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143711590..143711698 26863196 MeRIP-seq:(Medium) rs1554617461 Functional Loss SNV dbSNP153 33..33 33 - - - 64683 RMVar_ID_64683 Human_SNP_ID_386044331 m1A Human chr8 - 143716445 143716445 143716445 CCCTCGGCGCGCGGACGCACCCCCAGGCACTCACCCCCTGCCCGAGCTGCCGCCTGAGTAGGTAT CCCTCGGCGCGCGGACGCACCCCCAGGCACTCGCCCCCTGCCCGAGCTGCCGCCTGAGTAGGTAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143716394..143716551 26863196 MeRIP-seq:(Medium) rs567448822 Functional Loss SNV dbSNP153 33..33 33 - - - 64684 RMVar_ID_64684 Human_SNP_ID_386044432 m1A Human chr8 - 143716787 143716787 143716787 CCTGAGCCTGGGGTCCGCCCTTCCTCTCAGTGACCCGGGCGCGGGCCCAGCCTCCCCAGAGCGTC CCTGAGCCTGGGGTCCGCCCTTCCTCTCAGTGCCCCGGGCGCGGGCCCAGCCTCCCCAGAGCGTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143716774..143717085 26863196 MeRIP-seq:(Medium) rs1350724743 Functional Loss SNV dbSNP153 33..33 33 - - - 64685 RMVar_ID_64685 Human_SNP_ID_386044433 m1A Human chr8 - 143716791 143716791 143716791 TGCTCCTGAGCCTGGGGTCCGCCCTTCCTCTCAGTGACCCGGGCGCGGGCCCAGCCTCCCCAGAG TGCTCCTGAGCCTGGGGTCCGCCCTTCCTCTCTGTGACCCGGGCGCGGGCCCAGCCTCCCCAGAG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143716789..143716950 26863196 MeRIP-seq:(Medium) rs1333967965 Functional Loss SNV dbSNP153 33..33 33 - - - 64686 RMVar_ID_64686 Human_SNP_ID_386044434 m1A Human chr8 - 143716791 143716791 143716791 TGCTCCTGAGCCTGGGGTCCGCCCTTCCTCTCAGTGACCCGGGCGCGGGCCCAGCCTCCCCAGAG TGCTCCTGAGCCTGGGGTCCGCCCTTCCTCTCGGTGACCCGGGCGCGGGCCCAGCCTCCCCAGAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143716789..143716950 26863196 MeRIP-seq:(Medium) rs1333967965 Functional Loss SNV dbSNP153 33..33 33 - - - 64687 RMVar_ID_64687 Human_SNP_ID_386045187 m1A Human chr8 - 143718796 143718796 143718796 CGTGGACGTCCTGCAGCAGGCCGCCCTTCCGGATGACTGCGTTCAGGTCAGTGTCTGCAGAGAGG CGTGGACGTCCTGCAGCAGGCCGCCCTTCCGGGTGACTGCGTTCAGGTCAGTGTCTGCAGAGAGG T C AC105219.1 Ensembl:ENSG00000254548 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143718788..143718877 26863196 MeRIP-seq:(Medium) rs1446788544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24249870 Human_Splice_Rec_1020437 64688 RMVar_ID_64688 Human_SNP_ID_386045587 m1A Human chr8 - 143719497 143719497 143719497 TCTGACCTGCAGCATTCCCGGTGCCCAGCCCCAGCAGCCTGGCTCACCCTCCTCAGATGGCGGTG TCTGACCTGCAGCATTCCCGGTGCCCAGCCCCCGCAGCCTGGCTCACCCTCCTCAGATGGCGGTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143719451..143719880 26863196 MeRIP-seq:(Medium) rs1554619311 Functional Loss SNV dbSNP153 33..33 33 - - - 64689 RMVar_ID_64689 Human_SNP_ID_386046467 m1A Human chr8 + 143721616 143721616 143721616 AACTCCGCTCCCCTGCTCCAAACTGCTCTCCTAGGGAATGGGGAAAGGCCCCCTGGGGCGAAGGA AACTCCGCTCCCCTGCTCCAAACTGCTCTCCTCGGGAATGGGGAAAGGCCCCCTGGGGCGAAGGA A C MAPK15 Ensembl:ENSG00000181085 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143721526..143721635 26863196 MeRIP-seq:(Medium) rs1254636486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1020366,Human_Splice_Rec_1020367,Human_Splice_Rec_1020394,Human_Splice_Rec_1020395,Human_Splice_Rec_1020433,Human_Splice_Rec_1020435 64690 RMVar_ID_64690 Human_SNP_ID_386047398 m1A Human chr8 - 143724131 143724131 143724131 GGAAGCGGGATGCGCCTGTGCGTCTCTTGGCCATGATGTTCTTGTGGGCATGTTATTCTTGGTGC GGAAGCGGGATGCGCCTGTGCGTCTCTTGGCCGTGATGTTCTTGTGGGCATGTTATTCTTGGTGC T C FAM83H Ensembl:ENSG00000180921 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143724081..143724181 32194978 MeRIP-seq:(Medium) rs1194054294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695593,Human_RBP_ID_9354933,Human_RBP_ID_18388200 Human_miRNA_ID_688454,Human_miRNA_ID_879531,Human_miRNA_ID_1348977,Human_miRNA_ID_1812778,Human_miRNA_ID_2276598 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_97321,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930,RMVar_hsa_circ_254928 64691 RMVar_ID_64691 Human_SNP_ID_386047541 m1A Human chr8 + 143724626 143724626 143724626 GGGGGTGTCTGCTGGATACCAGGAGGACAAGGACCACTCCCACCTGCAGGGGTGCCCAGGACCTA GGGGGTGTCTGCTGGATACCAGGAGGACAAGGGCCACTCCCACCTGCAGGGGTGCCCAGGACCTA A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143724577..143724875 32194978 MeRIP-seq:(Medium) rs1207165177 Functional Loss SNV dbSNP153 33..33 33 - - - 64692 RMVar_ID_64692 Human_SNP_ID_386047976 m1A Human chr8 + 143725614 143725614 143725614 AAAATAAAGGGGGCGGGGGGGACTGAGGCACAAAGAGATGGCGGAGCCAGACGCTGCGCCACGCA AAAATAAAGGGGGCGGGGGGGACTGAGGCACAGAGAGATGGCGGAGCCAGACGCTGCGCCACGCA A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143725604..143725715 26863196 MeRIP-seq:(Medium) rs1489437061 Functional Loss SNV dbSNP153 33..33 33 - - - 64693 RMVar_ID_64693 Human_SNP_ID_386048351 m1A Human chr8 - 143726327 143726327 143726327 CAACCTTCGGGATGACACGAAGGCCATTCTGGAGCAGATCAGTGCCCACGGCCAGAAGCACCGTG CAACCTTCGGGATGACACGAAGGCCATTCTGGGGCAGATCAGTGCCCACGGCCAGAAGCACCGTG T C FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143726278..143726484 26863196 MeRIP-seq:(Medium) rs554572078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21905615 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 64694 RMVar_ID_64694 Human_SNP_ID_386048378 m1A Human chr8 - 143726386 143726386 143726386 GAAGAGCGGGGTCCGCGGGCGCGCCTGTCCTCAGCCACGGCCAACGCCTTGTACAGCAGCAACCT GAAGAGCGGGGTCCGCGGGCGCGCCTGTCCTCGGCCACGGCCAACGCCTTGTACAGCAGCAACCT T C FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143726351..143726425 26863196 MeRIP-seq:(Medium) rs1563757051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_101441,Human_miRNA_ID_1962007,Human_miRNA_ID_2027214 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 64695 RMVar_ID_64695 Human_SNP_ID_386048908 m1A Human chr8 + 143727170 143727170 143727170 CCGCCACCTCTTCCCGCCACGCCTGGGACACGACGGCCTTGCTGTGGCTGGCAACGGTGATGGCG CCGCCACCTCTTCCCGCCACGCCTGGGACACGCCGGCCTTGCTGTGGCTGGCAACGGTGATGGCG A C RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143727124..143727246 26863196 MeRIP-seq:(Medium) rs782617461 Functional Loss SNV dbSNP153 33..33 33 - - - 64696 RMVar_ID_64696 Human_SNP_ID_386049063 m1A Human chr8 - 143727380 143727380 143727380 CTCCTCGCTCATCTTCAGCACGTCACAGGCCGAGGGCGCGGCCGGGGCTGCGGCGGCCACTGAGA CTCCTCGCTCATCTTCAGCACGTCACAGGCCGTGGGCGCGGCCGGGGCTGCGGCGGCCACTGAGA T A FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143727329..143727517 26863196 MeRIP-seq:(Medium) rs115863410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845285,Human_RBP_ID_23259442,Human_RBP_ID_27536468 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 64697 RMVar_ID_64697 Human_SNP_ID_386049123 m1A Human chr8 - 143727485 143727485 143727485 CGGCAACGGCCCAGAGCGCGAGGGCCCGGAGGAGCCTGGCCTGGCCAAGCAGGACTCATTCCGCT CGGCAACGGCCCAGAGCGCGAGGGCCCGGAGGGGCCTGGCCTGGCCAAGCAGGACTCATTCCGCT T C FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143727151..143728050 26863196 MeRIP-seq:(Medium) rs782819198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27536468 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 64698 RMVar_ID_64698 Human_SNP_ID_386049287 m1A Human chr8 + 143727720 143727720 143727720 GTGGCAGCCGCTCAAGTAGGAGGCCAAACGCCAGCGCCGCAGCCCTGCCCGCCCCTCGGGCCCGC GTGGCAGCCGCTCAAGTAGGAGGCCAAACGCCGGCGCCGCAGCCCTGCCCGCCCCTCGGGCCCGC A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143727674..143727763 26863196 MeRIP-seq:(Medium) rs1320762162 Functional Loss SNV dbSNP153 33..33 33 - - - 64699 RMVar_ID_64699 Human_SNP_ID_386049593 m1A Human chr8 - 143728178 143728178 143728178 GGGCGCCGTGGAGAACTTCGCGGCCGCGCGGCAGGTGTCGCGGCAGACGTTCCTCAGCCACGGCG GGGCGCCGTGGAGAACTTCGCGGCCGCGCGGCGGGTGTCGCGGCAGACGTTCCTCAGCCACGGCG T C FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143728131..143728224 26863196 MeRIP-seq:(Medium) rs1158917585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2455334 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 64700 RMVar_ID_64700 Human_SNP_ID_386051756 m1A Human chr8 + 143733925 143733925 143733925 CGCCCGCATTCCTGCGCCCCGCGCCCGCCGCCAGCCCCAGCCCGCGCCCCCGGCCCGCGCCCCGA CGCCCGCATTCCTGCGCCCCGCGCCCGCCGCCCGCCCCAGCCCGCGCCCCCGGCCCGCGCCCCGA A C RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143733837..143734049 26863196 MeRIP-seq:(Medium) rs1405388234 Functional Loss SNV dbSNP153 33..33 33 - - - 64701 RMVar_ID_64701 Human_SNP_ID_386051757 m1A Human chr8 + 143733925 143733925 143733925 CGCCCGCATTCCTGCGCCCCGCGCCCGCCGCCAGCCCCAGCCCGCGCCCCCGGCCCGCGCCCCGA CGCCCGCATTCCTGCGCCCCGCGCCCGCCGCCGGCCCCAGCCCGCGCCCCCGGCCCGCGCCCCGA A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143733837..143734049 26863196 MeRIP-seq:(Medium) rs1405388234 Functional Loss SNV dbSNP153 33..33 33 - - - 64702 RMVar_ID_64702 Human_SNP_ID_386062165 m1A Human chr8 - 143770307 143770307 143770307 GCAGAGACTGACAATGCAAGCAAAGAGCAAACACTCAAGATAAAACCCAGGAAATCCTGAAATGA GCAGAGACTGACAATGCAAGCAAAGAGCAAACGCTCAAGATAAAACCCAGGAAATCCTGAAATGA T C AC105219.3 Ensembl:ENSG00000254973 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143770305..143770590 26863196 MeRIP-seq:(Medium) rs1214765314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3889101,Human_RBP_ID_5106408 64703 RMVar_ID_64703 Human_SNP_ID_386062493 m1A Human chr8 + 143771536 143771536 143771536 AGCGGCCAGAGCGATCCAGGGCGCCTTCCGGCAGCTCCGGGCCAGGAGGGAGCTCGCCCGCCGCC AGCGGCCAGAGCGATCCAGGGCGCCTTCCGGCCGCTCCGGGCCAGGAGGGAGCTCGCCCGCCGCC A C IQANK1 Ensembl:ENSG00000203499 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143771530..143771754 26863196 MeRIP-seq:(Medium) rs1381950524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1020468,Human_Splice_Rec_1020469 64704 RMVar_ID_64704 Human_SNP_ID_386068095 m1A Human chr8 + 143791175 143791175 143791175 TGGGGGAGGTGCCTGCTCCTCTAGGAGGGCACAGGGCCCAGGCCACGGCGCCCAGGCCTTACGGG TGGGGGAGGTGCCTGCTCCTCTAGGAGGGCACGGGGCCCAGGCCACGGCGCCCAGGCCTTACGGG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143791126..143791175 26863196 MeRIP-seq:(Medium) rs1441719309 Functional Loss SNV dbSNP153 33..33 33 - - - 64705 RMVar_ID_64705 Human_SNP_ID_386068635 m1A Human chr8 + 143792123 143792123 143792123 GACCATCTGTGCTCGGAGAGCGTCCTGTTCCAATGACTTCATCCTGCAGAGAACAGCGGGCAGGG GACCATCTGTGCTCGGAGAGCGTCCTGTTCCAGTGACTTCATCCTGCAGAGAACAGCGGGCAGGG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143792001..143792134 26863196 MeRIP-seq:(Medium) rs1359467237 Functional Loss SNV dbSNP153 33..33 33 - - - 64706 RMVar_ID_64706 Human_SNP_ID_386068694 m1A Human chr8 - 143792244 143792244 143792244 CCCTGCCGAGCTCCGGGCCCTGGAGGCCGAGAAGCGTGCGCTGTGGAGGGCAGCCAGGTGAGCCC CCCTGCCGAGCTCCGGGCCCTGGAGGCCGAGAGGCGTGCGCTGTGGAGGGCAGCCAGGTGAGCCC T C SCRIB Ensembl:ENSG00000180900 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143792226..143792250 26863196 MeRIP-seq:(Medium) rs897669030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19023163,Human_RBP_ID_22516715 Human_Splice_Rec_1020567,Human_Splice_Rec_1020637,Human_Splice_Rec_1020653,Human_Splice_Rec_1020677,Human_Splice_Rec_1020747,Human_Splice_Rec_1020819 64707 RMVar_ID_64707 Human_SNP_ID_386068918 m1A Human chr8 + 143792602 143792602 143792602 TCGCTTCGGCCCCAGCCTCTGCCGCCTCCCGCAGCATCTGCGCTCTCTTCTGCTGTAGTTTTCTG TCGCTTCGGCCCCAGCCTCTGCCGCCTCCCGCGGCATCTGCGCTCTCTTCTGCTGTAGTTTTCTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:143792473..143792875;chr8:143792472..143792816 26863196 MeRIP-seq:(Medium) rs1467829946 Functional Loss SNV dbSNP153 33..33 33 - - - 64708 RMVar_ID_64708 Human_SNP_ID_386070026 m1A Human chr8 - 143795335 143795335 143795335 GGTGCCTGACGGGTCTGCTCTGCTCTGCTCACAGGAGAAGGAGCTGCCTGGACAGACCCTGCACT GGTGCCTGACGGGTCTGCTCTGCTCTGCTCACGGGAGAAGGAGCTGCCTGGACAGACCCTGCACT T C SCRIB Ensembl:ENSG00000180900 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143794231..143803534 32194978 MeRIP-seq:(Medium) rs781889500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1335126 Human_Splice_Rec_1020553,Human_Splice_Rec_1020625,Human_Splice_Rec_1020667,Human_Splice_Rec_1020735,Human_Splice_Rec_1020807 RMVar_hsa_circ_80639,RMVar_hsa_circ_254938 64709 RMVar_ID_64709 Human_SNP_ID_386073256 m1A Human chr8 - 143804651 143804651 143804651 CCACCGCTGCTGTTGCCACCACCAGCATAACCACTGCCACCCCCGGGGTGCCTGGGTTGCCGAGC CCACCGCTGCTGTTGCCACCACCAGCATAACCGCTGCCACCCCCGGGGTGCCTGGGTTGCCGAGC T C SCRIB Ensembl:ENSG00000180900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143804601..143804982 26863196 MeRIP-seq:(Medium) rs1180633402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22534428 Human_Splice_Rec_1020543,Human_Splice_Rec_1020615,Human_Splice_Rec_1020725,Human_Splice_Rec_1020797 Human_miRNA_ID_2057726,Human_miRNA_ID_2457135,Human_miRNA_ID_2462057,Human_miRNA_ID_2634702,Human_miRNA_ID_2637389 RMVar_hsa_circ_80639,RMVar_hsa_circ_101342,RMVar_hsa_circ_117072,RMVar_hsa_circ_254938,RMVar_hsa_circ_111700,RMVar_hsa_circ_254939,RMVar_hsa_circ_108492,RMVar_hsa_circ_254940,RMVar_hsa_circ_254941,RMVar_hsa_circ_254942 64710 RMVar_ID_64710 Human_SNP_ID_386073704 m1A Human chr8 + 143805332 143805332 143805332 GCGGCGTGATGGTGACCGCGTTCTCAGGCTCCACCATGCGCTCCCGCCACACTCGCATCTGCACG GCGGCGTGATGGTGACCGCGTTCTCAGGCTCCCCCATGCGCTCCCGCCACACTCGCATCTGCACG A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:143805230..143805380 26863410 MeRIP-seq:(Medium) rs1554636280 Functional Loss SNV dbSNP153 33..33 33 - - - 64711 RMVar_ID_64711 Human_SNP_ID_386074353 m1A Human chr8 + 143806987 143806987 143806987 TTGCCGCCCGCAATGCTGATGCCCAGGCCCCCAGTCTGCCGCAGGATAGTGAGGGTCAGCTGGAA TTGCCGCCCGCAATGCTGATGCCCAGGCCCCCGGTCTGCCGCAGGATAGTGAGGGTCAGCTGGAA A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143806901..143807025 26863196 MeRIP-seq:(Medium) rs781990715 Functional Loss SNV dbSNP153 33..33 33 - - - 64712 RMVar_ID_64712 Human_SNP_ID_386075235 m1A Human chr8 - 143809015 143809015 143809015 CCTCACCCTTTTGTCCGCACAGCCCACGGTGCATTTCGCAGAGGACGCACTGCTGCCCGGGGATG CCTCACCCTTTTGTCCGCACAGCCCACGGTGCGTTTCGCAGAGGACGCACTGCTGCCCGGGGATG T C SCRIB Ensembl:ENSG00000180900 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143809001..143809025 26863196 MeRIP-seq:(Medium) rs537760051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8923250,Human_RBP_ID_22516721,Human_RBP_ID_22534432,Human_RBP_ID_26359434 Human_Splice_Rec_1020530,Human_Splice_Rec_1020602,Human_Splice_Rec_1020712,Human_Splice_Rec_1020784 64713 RMVar_ID_64713 Human_SNP_ID_386075738 m1A Human chr8 + 143810110 143810110 143810110 CAAAAACCCACAGCACGCATGTCACAGCTCTGAGTGAGAACAGTCAGGCCTGCTCTGTCCCAGTC CAAAAACCCACAGCACGCATGTCACAGCTCTGGGTGAGAACAGTCAGGCCTGCTCTGTCCCAGTC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143810104..143810529 26863196 MeRIP-seq:(Medium) rs1393117109 Functional Loss SNV dbSNP153 33..33 33 - - - 64714 RMVar_ID_64714 Human_SNP_ID_386075927 m1A Human chr8 - 143810584 143810584 143810584 TCCCTACAACAGGGCCTACAGCGCCGGGCCACACCTCACCCCAGCGAGCTCAAGGTGATGAAGAG TCCCTACAACAGGGCCTACAGCGCCGGGCCACGCCTCACCCCAGCGAGCTCAAGGTGATGAAGAG T C SCRIB Ensembl:ENSG00000180900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143810135..143810608 26863196 MeRIP-seq:(Medium) rs1334193849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695637,Human_RBP_ID_5406844,Human_RBP_ID_18125494 Human_Splice_Rec_1020526,Human_Splice_Rec_1020598,Human_Splice_Rec_1020708,Human_Splice_Rec_1020780 64715 RMVar_ID_64715 Human_SNP_ID_386078475 m1A Human chr8 + 143815447 143815447 143815447 GGCTCGGGGCCGGGGGGCGGGGCTCAGTCCGCATGGGCGCCGCGCATGGGGAGGGGGCGCAGGCA GGCTCGGGGCCGGGGGGCGGGGCTCAGTCCGCCTGGGCGCCGCGCATGGGGAGGGGGCGCAGGCA A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr8:143815226..143815775;chr8:143815346..143815733 26863196,26863410 MeRIP-seq:(Medium) rs1364303210 Functional Loss SNV dbSNP153 33..33 33 - - - 64716 RMVar_ID_64716 Human_SNP_ID_386078476 m1A Human chr8 + 143815447 143815447 143815447 GGCTCGGGGCCGGGGGGCGGGGCTCAGTCCGCATGGGCGCCGCGCATGGGGAGGGGGCGCAGGCA GGCTCGGGGCCGGGGGGCGGGGCTCAGTCCGCTTGGGCGCCGCGCATGGGGAGGGGGCGCAGGCA A T RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr8:143815226..143815775;chr8:143815346..143815733 26863196,26863410 MeRIP-seq:(Medium) rs1364303210 Functional Loss SNV dbSNP153 33..33 33 - - - 64717 RMVar_ID_64717 Human_SNP_ID_386078482 m1A Human chr8 + 143815479 143815461 143815480 ATGGGCGCCGCGCATGGGGAGGGGGCGCAGGCAGGGGGCGGGCCGCCCGAGACTGGACGGGGACG ATGGGCGCCGCGCAT___________________GGGGCGGGCCGCCCGAGACTGGACGGGGACG TGGGGAGGGGGCGCAGGCAG T RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:143815388..143815568 26863410 MeRIP-seq:(Medium) rs1041435289 Functional Loss DEL dbSNP153 16..34 33 - - - 64718 RMVar_ID_64718 Human_SNP_ID_386078505 m1A Human chr8 + 143815498 143815498 143815498 AGGGGGCGCAGGCAGGGGGCGGGCCGCCCGAGACTGGACGGGGACGCGGCCGCGGCCGGCGCTGG AGGGGGCGCAGGCAGGGGGCGGGCCGCCCGAGGCTGGACGGGGACGCGGCCGCGGCCGGCGCTGG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143815448..143815568 32194978 MeRIP-seq:(Medium) rs1243518208 Functional Loss SNV dbSNP153 33..33 33 - - - 64719 RMVar_ID_64719 Human_SNP_ID_386078516 m1A Human chr8 - 143815528 143815528 143815528 CAGTCCGAGCGTTCCGAGCGCGGGCCGGGCCCAGCGCCGGCCGCGGCCGCGTCCCCGTCCAGTCT CAGTCCGAGCGTTCCGAGCGCGGGCCGGGCCCGGCGCCGGCCGCGGCCGCGTCCCCGTCCAGTCT T C SCRIB Ensembl:ENSG00000180900 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:143815276..143815725 26863410 MeRIP-seq:(Medium) rs1554639742 Functional Loss SNV dbSNP153 33..33 33 - - - 64720 RMVar_ID_64720 Human_SNP_ID_386078585 m1A Human chr8 - 143815687 143815676 143815688 TCCGGCGGGCAGCGGCGGTTCCGGTGCGGCACAGCGGGCGGACGAGCGGGCGGGACGAGCTGAGC TCCGGCGGGCAGCGGCGGTTCCGGTGCGGCA____________GAGCGGGCGGGACGAGCTGAGC CGTCCGCCCGCTG C SCRIB Ensembl:ENSG00000180900 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr8:143815301..143815800;chr8:143815273..143815825;chr8:143815280..143815825;chr8:143815473..143815850;chr8:143815439..143815850 26863196 MeRIP-seq:(Medium) rs1012753299 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_27569690 64721 RMVar_ID_64721 Human_SNP_ID_386078622 m1A Human chr8 - 143815771 143815771 143815771 GCAGTCCGGGCGTGCTAGGCGGCGAGGGCCGGACTCGGCTTCCCGACGGGCTGCGCGGCGGCCGG GCAGTCCGGGCGTGCTAGGCGGCGAGGGCCGGGCTCGGCTTCCCGACGGGCTGCGCGGCGGCCGG T C SCRIB Ensembl:ENSG00000180900 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:143815692..143815776 26863410 MeRIP-seq:(Medium) rs1417030681 Functional Loss SNV dbSNP153 33..33 33 - - - 64722 RMVar_ID_64722 Human_SNP_ID_386079271 m1A Human chr8 - 143817006 143817006 143817006 GAGAAGGAAGAAGAGGAGCTGTTTCCCGAGTCAGAGCGGCCAGAGATGCTGAGCGAGCAGGAGCA GAGAAGGAAGAAGAGGAGCTGTTTCCCGAGTCGGAGCGGCCAGAGATGCTGAGCGAGCAGGAGCA T C PUF60 Ensembl:ENSG00000179950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143816475..143817098 26863196 MeRIP-seq:(Medium) rs559702760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15232,Human_RBP_ID_89226,Human_RBP_ID_3974183,Human_RBP_ID_4973949,Human_RBP_ID_8682879,Human_RBP_ID_8923629,Human_RBP_ID_18196782,Human_RBP_ID_19023191,Human_RBP_ID_22465035,Human_RBP_ID_24549481,Human_RBP_ID_26359444 Human_Splice_Rec_1020865,Human_Splice_Rec_1020887,Human_Splice_Rec_1020907,Human_Splice_Rec_1020927,Human_Splice_Rec_1020947,Human_Splice_Rec_1020965 Human_miRNA_ID_2453862 RMVar_hsa_circ_85067,RMVar_hsa_circ_126033,RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_87285,RMVar_hsa_circ_254952,RMVar_hsa_circ_254954,RMVar_hsa_circ_254956,RMVar_hsa_circ_77730,RMVar_hsa_circ_254955,RMVar_hsa_circ_254953,RMVar_hsa_circ_254951,RMVar_hsa_circ_254957,RMVar_hsa_circ_109305 64723 RMVar_ID_64723 Human_SNP_ID_386079272 m1A Human chr8 - 143817006 143817006 143817006 GAGAAGGAAGAAGAGGAGCTGTTTCCCGAGTCAGAGCGGCCAGAGATGCTGAGCGAGCAGGAGCA GAGAAGGAAGAAGAGGAGCTGTTTCCCGAGTCCGAGCGGCCAGAGATGCTGAGCGAGCAGGAGCA T G PUF60 Ensembl:ENSG00000179950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143816475..143817098 26863196 MeRIP-seq:(Medium) rs559702760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15232,Human_RBP_ID_89226,Human_RBP_ID_3974183,Human_RBP_ID_4973949,Human_RBP_ID_8682879,Human_RBP_ID_8923629,Human_RBP_ID_18196782,Human_RBP_ID_19023191,Human_RBP_ID_22465035,Human_RBP_ID_24549481,Human_RBP_ID_26359444 Human_Splice_Rec_1020865,Human_Splice_Rec_1020887,Human_Splice_Rec_1020907,Human_Splice_Rec_1020927,Human_Splice_Rec_1020947,Human_Splice_Rec_1020965 Human_miRNA_ID_2453862 RMVar_hsa_circ_85067,RMVar_hsa_circ_126033,RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_87285,RMVar_hsa_circ_254952,RMVar_hsa_circ_254954,RMVar_hsa_circ_254956,RMVar_hsa_circ_77730,RMVar_hsa_circ_254955,RMVar_hsa_circ_254953,RMVar_hsa_circ_254951,RMVar_hsa_circ_254957,RMVar_hsa_circ_109305 64724 RMVar_ID_64724 Human_SNP_ID_386079281 m1A Human chr8 - 143817022 143817020 143817023 CCTGGAGCCCAAGAAGGAGAAGGAAGAAGAGGAGCTGTTTCCCGAGTCAGAGCGGCCAGAGATGC CCTGGAGCCCAAGAAGGAGAAGGAAGAAGAG___CTGTTTCCCGAGTCAGAGCGGCCAGAGATGC GCTC G PUF60 Ensembl:ENSG00000179950 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143816973..143817088 26863196 MeRIP-seq:(Medium) rs1489383612 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_89226,Human_RBP_ID_3874704,Human_RBP_ID_18196782,Human_RBP_ID_19023191,Human_RBP_ID_22836542,Human_RBP_ID_24549481,Human_RBP_ID_26359444 Human_miRNA_ID_2453862 RMVar_hsa_circ_85067,RMVar_hsa_circ_126033,RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_87285,RMVar_hsa_circ_254952,RMVar_hsa_circ_254954,RMVar_hsa_circ_254956,RMVar_hsa_circ_77730,RMVar_hsa_circ_254955,RMVar_hsa_circ_254953,RMVar_hsa_circ_254951,RMVar_hsa_circ_254957,RMVar_hsa_circ_109305 64725 RMVar_ID_64725 Human_SNP_ID_386080232 m1A Human chr8 - 143819682 143819680 143819682 TCTTGCTCTGAGTGGGGAGCCTGAGGTCTGTCAGGGGGCCCAGTGTGAGGAGAACACAGTCTCGT TCTTGCTCTGAGTGGGGAGCCTGAGGTCTGTC__GGGGCCCAGTGTGAGGAGAACACAGTCTCGT CCT C PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143819680..143819901 26863196 MeRIP-seq:(Medium) rs1223404282 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1223956,Human_RBP_ID_5406071,Human_RBP_ID_8155094,Human_RBP_ID_8730889,Human_RBP_ID_16380349,Human_RBP_ID_19143010,Human_RBP_ID_22688597 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_105116,RMVar_hsa_circ_254960 64726 RMVar_ID_64726 Human_SNP_ID_386080355 m1A Human chr8 - 143820067 143820064 143820067 TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGGAGGTGTCCCTCCCTTCCCCCAGAGGCAGGCTCA TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGG___TGTCCCTCCCTTCCCCCAGAGGCAGGCTCA ACCT A PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143820064..143820243 26863196 MeRIP-seq:(Medium) rs1256624969 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_255097,Human_RBP_ID_268248,Human_RBP_ID_958630,Human_RBP_ID_3886446,Human_RBP_ID_9441029,Human_RBP_ID_18961262,Human_RBP_ID_22747617 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_105116,RMVar_hsa_circ_254960 64727 RMVar_ID_64727 Human_SNP_ID_386080358 m1A Human chr8 - 143820067 143820067 143820067 TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGGAGGTGTCCCTCCCTTCCCCCAGAGGCAGGCTCA TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGGTGGTGTCCCTCCCTTCCCCCAGAGGCAGGCTCA T A PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143820064..143820243 26863196 MeRIP-seq:(Medium) rs533484550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255097,Human_RBP_ID_268248,Human_RBP_ID_958630,Human_RBP_ID_3886446,Human_RBP_ID_9441029,Human_RBP_ID_18961262,Human_RBP_ID_22747617 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_105116,RMVar_hsa_circ_254960 64728 RMVar_ID_64728 Human_SNP_ID_386080359 m1A Human chr8 - 143820067 143820067 143820067 TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGGAGGTGTCCCTCCCTTCCCCCAGAGGCAGGCTCA TTGGCTGTGGTGGGCAGAGGAGTGTGGGAAGGCGGTGTCCCTCCCTTCCCCCAGAGGCAGGCTCA T G PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143820064..143820243 26863196 MeRIP-seq:(Medium) rs533484550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255097,Human_RBP_ID_268248,Human_RBP_ID_958630,Human_RBP_ID_3886446,Human_RBP_ID_9441029,Human_RBP_ID_18961262,Human_RBP_ID_22747617 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_105116,RMVar_hsa_circ_254960 64729 RMVar_ID_64729 Human_SNP_ID_386080930 m1A Human chr8 - 143821888 143821888 143821888 TTACCAGGGCACAGACTCCATCAAGATGGAGAACGGGCAGAGCACAGCCGCCAAGCTGGGGCTGC TTACCAGGGCACAGACTCCATCAAGATGGAGAGCGGGCAGAGCACAGCCGCCAAGCTGGGGCTGC T C PUF60 Ensembl:ENSG00000179950 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143821521..143822516 32194978 MeRIP-seq:(Medium) rs1451251368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255100,Human_RBP_ID_957917,Human_RBP_ID_22534433,Human_RBP_ID_22689429,Human_RBP_ID_26360222 Human_Splice_Rec_1020848,Human_Splice_Rec_1020849,Human_Splice_Rec_1020870,Human_Splice_Rec_1020871,Human_Splice_Rec_1020892,Human_Splice_Rec_1020893,Human_Splice_Rec_1020910,Human_Splice_Rec_1020911,Human_Splice_Rec_1020932,Human_Splice_Rec_1020933,Human_Splice_Rec_1020950,Human_Splice_Rec_1020951,Human_Splice_Rec_1020968,Human_Splice_Rec_1020969,Human_Splice_Rec_1020998,Human_Splice_Rec_1020999,Human_Splice_Rec_1021012,Human_Splice_Rec_1021013,Human_Splice_Rec_1021030,Human_Splice_Rec_1021031,Human_Splice_Rec_1021042,Human_Splice_Rec_1021043,Human_Splice_Rec_1021052,Human_Splice_Rec_1021053,Human_Splice_Rec_1021072,Human_Splice_Rec_1021073,Human_Splice_Rec_1021088,Human_Splice_Rec_1021089,Human_Splice_Rec_1021098,Human_Splice_Rec_1021099,Human_Splice_Rec_1021110,Human_Splice_Rec_1021111,Human_Splice_Rec_1021118,Human_Splice_Rec_1021119,Human_Splice_Rec_1021124,Human_Splice_Rec_1021125 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_105116,RMVar_hsa_circ_123416,RMVar_hsa_circ_254960,RMVar_hsa_circ_254961 64730 RMVar_ID_64730 Human_SNP_ID_386081724 m1A Human chr8 - 143824349 143824349 143824349 GGAGGGGGGTCCGAGCCGGCGGCGGCGGCGGCAGTGGTGGCAGCGGGAGACAAATGGAAACCTCC GGAGGGGGGTCCGAGCCGGCGGCGGCGGCGGCCGTGGTGGCAGCGGGAGACAAATGGAAACCTCC T G PUF60 Ensembl:ENSG00000179950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143824265..143824415 26863196 MeRIP-seq:(Medium) rs892972873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255102,Human_RBP_ID_957918,Human_RBP_ID_4995776,Human_RBP_ID_5328991,Human_RBP_ID_22465687,Human_RBP_ID_24555246,Human_RBP_ID_26359450,Human_RBP_ID_27122186 Human_Splice_Rec_1020846,Human_Splice_Rec_1020847,Human_Splice_Rec_1020868,Human_Splice_Rec_1020869,Human_Splice_Rec_1020890,Human_Splice_Rec_1020891,Human_Splice_Rec_1020930,Human_Splice_Rec_1020931,Human_Splice_Rec_1020996,Human_Splice_Rec_1020997,Human_Splice_Rec_1021010,Human_Splice_Rec_1021011,Human_Splice_Rec_1021028,Human_Splice_Rec_1021029,Human_Splice_Rec_1021041,Human_Splice_Rec_1021050,Human_Splice_Rec_1021051,Human_Splice_Rec_1021070,Human_Splice_Rec_1021071,Human_Splice_Rec_1021086,Human_Splice_Rec_1021087,Human_Splice_Rec_1021097,Human_Splice_Rec_1021108,Human_Splice_Rec_1021109,Human_Splice_Rec_1021116,Human_Splice_Rec_1021117,Human_Splice_Rec_1021122,Human_Splice_Rec_1021123 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955,RMVar_hsa_circ_123416,RMVar_hsa_circ_254961 64731 RMVar_ID_64731 Human_SNP_ID_386082758 m1A Human chr8 - 143827531 143827531 143827531 CCTGTCCCCTGTCTCATGCTGCTTCAGCTCTCATGGGAGGTTGAATGGAGCAGCTGAACTTGGCT CCTGTCCCCTGTCTCATGCTGCTTCAGCTCTCGTGGGAGGTTGAATGGAGCAGCTGAACTTGGCT T C PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143827529..143829375 26863196 MeRIP-seq:(Medium) rs1450549512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1021048,Human_Splice_Rec_1021068,Human_Splice_Rec_1021084 Human_miRNA_ID_2047382,Human_miRNA_ID_2214218 RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955 64732 RMVar_ID_64732 Human_SNP_ID_386083433 m1A Human chr8 - 143829322 143829322 143829322 GCGGAAGGAGCAAGAGTGGGAGGCGCGCGCGGAGGCCGCGACGGACGCAAGATGGCGACGGCGAC GCGGAAGGAGCAAGAGTGGGAGGCGCGCGCGGGGGCCGCGACGGACGCAAGATGGCGACGGCGAC T C PUF60 Ensembl:ENSG00000179950 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143827479..143829461;chr8:143827529..143829375;chr8:143829215..143829375 26863196 MeRIP-seq:(Medium) rs782745717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4974009,Human_RBP_ID_26360223 Human_Splice_Rec_1020845,Human_Splice_Rec_1020909,Human_Splice_Rec_1020929,Human_Splice_Rec_1020949,Human_Splice_Rec_1020995,Human_Splice_Rec_1021009,Human_Splice_Rec_1021067,Human_Splice_Rec_1021083,Human_Splice_Rec_1021107,Human_Splice_Rec_1021115 RMVar_hsa_circ_92361,RMVar_hsa_circ_254956 64733 RMVar_ID_64733 Human_SNP_ID_386083434 m1A Human chr8 - 143829322 143829322 143829322 GCGGAAGGAGCAAGAGTGGGAGGCGCGCGCGGAGGCCGCGACGGACGCAAGATGGCGACGGCGAC GCGGAAGGAGCAAGAGTGGGAGGCGCGCGCGGCGGCCGCGACGGACGCAAGATGGCGACGGCGAC T G PUF60 Ensembl:ENSG00000179950 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143827479..143829461;chr8:143827529..143829375;chr8:143829215..143829375 26863196 MeRIP-seq:(Medium) rs782745717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4974009,Human_RBP_ID_26360223 Human_Splice_Rec_1020845,Human_Splice_Rec_1020909,Human_Splice_Rec_1020929,Human_Splice_Rec_1020949,Human_Splice_Rec_1020995,Human_Splice_Rec_1021009,Human_Splice_Rec_1021067,Human_Splice_Rec_1021083,Human_Splice_Rec_1021107,Human_Splice_Rec_1021115 RMVar_hsa_circ_92361,RMVar_hsa_circ_254956 64734 RMVar_ID_64734 Human_SNP_ID_386085154 m1A Human chr8 + 143834813 143834813 143834813 CCAGGAGTGGAGTGGGAGAGAGGCAGGGAGCCAGGAGCTGACATCCTCAGAGGCCCAGGGAGCAG CCAGGAGTGGAGTGGGAGAGAGGCAGGGAGCCGGGAGCTGACATCCTCAGAGGCCCAGGGAGCAG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143834764..143835080 26863196 MeRIP-seq:(Medium) rs1202579384 Functional Loss SNV dbSNP153 33..33 33 - - - 64735 RMVar_ID_64735 Human_SNP_ID_386085396 m1A Human chr8 + 143835587 143835587 143835587 GTGCTCCCAGGCGCATGGAGGAGGGCAGCCCCACGGTGCTGGAGTCTCCCCAACATGGCCTGCCC GTGCTCCCAGGCGCATGGAGGAGGGCAGCCCCGCGGTGCTGGAGTCTCCCCAACATGGCCTGCCC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143835582..143835776 26863196 MeRIP-seq:(Medium) rs1217087154 Functional Loss SNV dbSNP153 33..33 33 - - - 64736 RMVar_ID_64736 Human_SNP_ID_386085423 m1A Human chr8 + 143835627 143835626 143835627 GGAGTCTCCCCAACATGGCCTGCCCAGGCAGCACCCCGGCATGGTCCCCTGGGGCTGGGGCTCCG GGAGTCTCCCCAACATGGCCTGCCCAGGCAGC_CCCCGGCATGGTCCCCTGGGGCTGGGGCTCCG CA C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143835577..143835747 26863196 MeRIP-seq:(Medium) rs1563857955 Functional Loss DEL dbSNP153 33..33 33 - - - 64737 RMVar_ID_64737 Human_SNP_ID_386086173 m1A Human chr8 - 143837159 143837159 143837159 CCCTGTTGTGTCCCCAGGAATGGAATCTACCCACTGATGAACTTTGCAGCCACTCGACCCCTGGG CCCTGTTGTGTCCCCAGGAATGGAATCTACCCGCTGATGAACTTTGCAGCCACTCGACCCCTGGG T C NRBP2 Ensembl:ENSG00000185189 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143837108..143837224 26863196 MeRIP-seq:(Medium) rs782629282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19023202 Human_Splice_Rec_1021156,Human_Splice_Rec_1021188,Human_Splice_Rec_1021214,Human_Splice_Rec_1021226,Human_Splice_Rec_1021262,Human_Splice_Rec_1021292,Human_Splice_Rec_1021304 Human_miRNA_ID_2768660 64738 RMVar_ID_64738 Human_SNP_ID_386087259 m1A Human chr8 - 143839569 143839569 143839569 AGCCGCCTCTCCTGCGCCCACCCGACCGACGGAGTCGTGCGTCCGCCGCCAGGCCTGGAAGCGCT AGCCGCCTCTCCTGCGCCCACCCGACCGACGGTGTCGTGCGTCCGCCGCCAGGCCTGGAAGCGCT T A NRBP2 Ensembl:ENSG00000185189 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143839426..143839708 26863196 MeRIP-seq:(Medium) rs1554653064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255124,Human_RBP_ID_5329334,Human_RBP_ID_5406089,Human_RBP_ID_9406612,Human_RBP_ID_19022262,Human_RBP_ID_19140485,Human_RBP_ID_21994934,Human_RBP_ID_26360228,Human_RBP_ID_27832210 Human_Splice_Rec_1021139,Human_Splice_Rec_1021171,Human_Splice_Rec_1021197,Human_Splice_Rec_1021245,Human_Splice_Rec_1021275,Human_Splice_Rec_1021319 RMVar_hsa_circ_16276,RMVar_hsa_circ_254962,RMVar_hsa_circ_85929 64739 RMVar_ID_64739 Human_SNP_ID_386087499 m1A Human chr8 - 143840217 143840217 143840217 AACCCTTTATTCACCCCCAGGTAAACCAAGGGAACATGCCAGGGCTTCAGAGCACCTTCCTAGCC AACCCTTTATTCACCCCCAGGTAAACCAAGGGTACATGCCAGGGCTTCAGAGCACCTTCCTAGCC T A NRBP2 Ensembl:ENSG00000185189 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143840113..143840352 26863196 MeRIP-seq:(Medium) rs56096760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1021132,Human_Splice_Rec_1021166,Human_Splice_Rec_1021312 RMVar_hsa_circ_254962,RMVar_hsa_circ_85929,RMVar_hsa_circ_254966,RMVar_hsa_circ_355097 64740 RMVar_ID_64740 Human_SNP_ID_386087500 m1A Human chr8 - 143840217 143840217 143840217 AACCCTTTATTCACCCCCAGGTAAACCAAGGGAACATGCCAGGGCTTCAGAGCACCTTCCTAGCC AACCCTTTATTCACCCCCAGGTAAACCAAGGGGACATGCCAGGGCTTCAGAGCACCTTCCTAGCC T C NRBP2 Ensembl:ENSG00000185189 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143840113..143840352 26863196 MeRIP-seq:(Medium) rs56096760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1021132,Human_Splice_Rec_1021166,Human_Splice_Rec_1021312 RMVar_hsa_circ_254962,RMVar_hsa_circ_85929,RMVar_hsa_circ_254966,RMVar_hsa_circ_355097 64741 RMVar_ID_64741 Human_SNP_ID_386087694 m1A Human chr8 + 143840884 143840884 143840884 CCACCGCCCTCTGCGCGATCCGCCGCCGGCGCAGCCTCTCCCGGCCCGCCCTGGCCTCGCGCCCA CCACCGCCCTCTGCGCGATCCGCCGCCGGCGCCGCCTCTCCCGGCCCGCCCTGGCCTCGCGCCCA A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143840751..143840950 26863196 MeRIP-seq:(Medium) rs1274799152 Functional Loss SNV dbSNP153 33..33 33 - - - 64742 RMVar_ID_64742 Human_SNP_ID_386090497 m1A Human chr8 + 143850965 143850965 143850965 CAGCACTGGAGGGAGTCAAGGGAAGACAAGCCAGGCATCTGAGCTCCTCTGTCTCTGCCTTTCCT CAGCACTGGAGGGAGTCAAGGGAAGACAAGCCGGGCATCTGAGCTCCTCTGTCTCTGCCTTTCCT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143850958..143851187 26863196 MeRIP-seq:(Medium) rs1242431953 Functional Loss SNV dbSNP153 33..33 33 - - - 64743 RMVar_ID_64743 Human_SNP_ID_386092838 m1A Human chr8 - 143858132 143858132 143858132 CTACCGGCGCGGCTACTTCGACGAGGAGATGAACCGCGTCCTGGCCGACCCCAGCGACGACACCA CTACCGGCGCGGCTACTTCGACGAGGAGATGAGCCGCGTCCTGGCCGACCCCAGCGACGACACCA T C EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143858085..143858217 26863196 MeRIP-seq:(Medium) rs782494150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8923254,Human_RBP_ID_9314068 64744 RMVar_ID_64744 Human_SNP_ID_386092839 m1A Human chr8 - 143858132 143858132 143858132 CTACCGGCGCGGCTACTTCGACGAGGAGATGAACCGCGTCCTGGCCGACCCCAGCGACGACACCA CTACCGGCGCGGCTACTTCGACGAGGAGATGACCCGCGTCCTGGCCGACCCCAGCGACGACACCA T G EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143858085..143858217 26863196 MeRIP-seq:(Medium) rs782494150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8923254,Human_RBP_ID_9314068 64745 RMVar_ID_64745 Human_SNP_ID_386095189 m1A Human chr8 - 143866915 143866915 143866915 CTGGAGGCAGAGCAAGTGGAAATCACAGTGGGAAGGTTCAGAGGCCAGAAACCAACACTGTGGGC CTGGAGGCAGAGCAAGTGGAAATCACAGTGGGGAGGTTCAGAGGCCAGAAACCAACACTGTGGGC T C EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143866867..143867067 26863196 MeRIP-seq:(Medium) rs782636871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90029,Human_RBP_ID_22731687 64746 RMVar_ID_64746 Human_SNP_ID_386095421 m1A Human chr8 - 143867189 143867189 143867189 GGCCACGGGGGGTGTCATCGACCCACAGCACCACCACCGGCTCCCACTGGAAACAGCCTACAGAC GGCCACGGGGGGTGTCATCGACCCACAGCACCCCCACCGGCTCCCACTGGAAACAGCCTACAGAC T G EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143867139..143867362 26863196 MeRIP-seq:(Medium) rs1237705176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996427,Human_RBP_ID_5534358,Human_RBP_ID_18196594,Human_RBP_ID_22534436,Human_RBP_ID_22732055 64747 RMVar_ID_64747 Human_SNP_ID_386096210 m1A Human chr8 + 143868424 143868424 143868424 CGGTTCTCCACGGGGTCGATGATGAAGCCGGTAGCTGCCTGTGCCTCCAGCAGCACCAGGGCTGT CGGTTCTCCACGGGGTCGATGATGAAGCCGGTGGCTGCCTGTGCCTCCAGCAGCACCAGGGCTGT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143868422..143868572 26863196 MeRIP-seq:(Medium) rs954912892 Functional Loss SNV dbSNP153 33..33 33 - - - 64748 RMVar_ID_64748 Human_SNP_ID_386096469 m1A Human chr8 - 143868824 143868824 143868824 CGTGTCACTCTGGGACCTGCTGCTCTCCGAATACGTTGGCGCTGACAAGCGGCGGGAGCTGGTGG CGTGTCACTCTGGGACCTGCTGCTCTCCGAATCCGTTGGCGCTGACAAGCGGCGGGAGCTGGTGG T G EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143868821..143868922 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1335148,Human_RBP_ID_1400791,Human_RBP_ID_4974109,Human_RBP_ID_8917224,Human_RBP_ID_9313645,Human_RBP_ID_22732061 64749 RMVar_ID_64749 Human_SNP_ID_386096990 m1A Human chr8 + 143869722 143869722 143869722 GAGCTTGGTCTCCTGTACCCACCTCTGCACAGAGGCTAGCAGCTGTGGCACAGTGGTCCTCCCCT GAGCTTGGTCTCCTGTACCCACCTCTGCACAGGGGCTAGCAGCTGTGGCACAGTGGTCCTCCCCT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143869720..143869970 26863196 MeRIP-seq:(Medium) rs1364932629 Functional Loss SNV dbSNP153 33..33 33 - - - 64750 RMVar_ID_64750 Human_SNP_ID_386097665 m1A Human chr8 + 143870984 143870984 143870984 AGAAGCCCTTGGTGTCGTCAGAAGGGTCCAACAGGATCAAGTTCAGCATCTGATCGAAGTAGCCG AGAAGCCCTTGGTGTCGTCAGAAGGGTCCAACGGGATCAAGTTCAGCATCTGATCGAAGTAGCCG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143870851..143871018 26863196 MeRIP-seq:(Medium) rs1328168315 Functional Loss SNV dbSNP153 33..33 33 - - - 64751 RMVar_ID_64751 Human_SNP_ID_386098101 m1A Human chr8 + 143871782 143871782 143871782 TCCCCACAGAGACGGTGGCTGTGGCCGTGCTCAGGGCCTGCCGAGTGCTGTACTTGATGAATGGG TCCCCACAGAGACGGTGGCTGTGGCCGTGCTCGGGGCCTGCCGAGTGCTGTACTTGATGAATGGG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143871779..143871879 26863196 MeRIP-seq:(Medium) rs782365594 Functional Loss SNV dbSNP153 33..33 33 - - - 64752 RMVar_ID_64752 Human_SNP_ID_386098277 m1A Human chr8 - 143872081 143872081 143872081 ATGAAGAAGGGGCTAGTGGACAGGCCACTGGCACTGCGGCTCTTGGATGCCCAGCTGGCCACAGG ATGAAGAAGGGGCTAGTGGACAGGCCACTGGCGCTGCGGCTCTTGGATGCCCAGCTGGCCACAGG T C EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143872078..143872179 26863196 MeRIP-seq:(Medium) rs1554661426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18196608,Human_RBP_ID_22731702 64753 RMVar_ID_64753 Human_SNP_ID_386098846 m1A Human chr8 - 143873154 143873154 143873154 CCAGAGCCATGGCAGCCACGCTGGGAGCCGGCACGCCCCCCAGGCCCCAGGCCAGGAGCATAGCT CCAGAGCCATGGCAGCCACGCTGGGAGCCGGCCCGCCCCCCAGGCCCCAGGCCAGGAGCATAGCT T G EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143873145..143873287 26863196 MeRIP-seq:(Medium) rs782248266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8923639,Human_RBP_ID_9314098 64754 RMVar_ID_64754 Human_SNP_ID_386098863 m1A Human chr8 - 143873178 143873178 143873178 ACAGCACAGAGCAGGCCAGTGTACCCAGAGCCATGGCAGCCACGCTGGGAGCCGGCACGCCCCCC ACAGCACAGAGCAGGCCAGTGTACCCAGAGCCGTGGCAGCCACGCTGGGAGCCGGCACGCCCCCC T C EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143873170..143873288 26863196 MeRIP-seq:(Medium) rs781796188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9314098 64755 RMVar_ID_64755 Human_SNP_ID_386099351 m1A Human chr8 + 143874737 143874737 143874737 CAGGAGCAGGGTCTGCTCCCCGTTTTCTCAGCACTACGGGCCCCAGTCCCTCTCTTGATTCTCCC CAGGAGCAGGGTCTGCTCCCCGTTTTCTCAGCGCTACGGGCCCCAGTCCCTCTCTTGATTCTCCC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143874732..143874859 26863196 MeRIP-seq:(Medium) rs1181415549 Functional Loss SNV dbSNP153 33..33 33 - - - 64756 RMVar_ID_64756 Human_SNP_ID_386100108 m1A Human chr8 - 143877308 143877308 143877308 CCCTGCCCCCCCTCGCTCCGGACCCTCTGTCCAGCTGCCCTCCCAGGCCCCACATGGAGTCAAGA CCCTGCCCCCCCTCGCTCCGGACCCTCTGTCCCGCTGCCCTCCCAGGCCCCACATGGAGTCAAGA T G EPPK1 Ensembl:ENSG00000261150 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:143877276..143877510;chr8:143877287..143877466 26863196 MeRIP-seq:(Medium) rs1279445810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3886461 64757 RMVar_ID_64757 Human_SNP_ID_386100479 m1A Human chr8 + 143878362 143878362 143878362 GCCGCCCCGCCCGGCCCCGAGCCCGCACCCGCACCCGCCGCACCTGCCCGCACCCGCCGCACCTG GCCGCCCCGCCCGGCCCCGAGCCCGCACCCGCCCCCGCCGCACCTGCCCGCACCCGCCGCACCTG A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143877755..143878461 26863196 MeRIP-seq:(Medium) rs1326947411 Functional Loss SNV dbSNP153 33..33 33 - - - 64758 RMVar_ID_64758 Human_SNP_ID_386100489 m1A Human chr8 + 143878371 143878370 143878371 CCCGGCCCCGAGCCCGCACCCGCACCCGCCGCACCTGCCCGCACCCGCCGCACCTGCCCGCACCC CCCGGCCCCGAGCCCGCACCCGCACCCGCCGC_CCTGCCCGCACCCGCCGCACCTGCCCGCACCC CA C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143877918..143878475;chr8:143877911..143878455 26863196 MeRIP-seq:(Medium) rs1425463348 Functional Loss DEL dbSNP153 33..33 33 - - - 64759 RMVar_ID_64759 Human_SNP_ID_386100490 m1A Human chr8 + 143878371 143878371 143878371 CCCGGCCCCGAGCCCGCACCCGCACCCGCCGCACCTGCCCGCACCCGCCGCACCTGCCCGCACCC CCCGGCCCCGAGCCCGCACCCGCACCCGCCGCCCCTGCCCGCACCCGCCGCACCTGCCCGCACCC A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143877918..143878475;chr8:143877911..143878455 26863196 MeRIP-seq:(Medium) rs1177717989 Functional Loss SNV dbSNP153 33..33 33 - - - 64760 RMVar_ID_64760 Human_SNP_ID_386100551 m1A Human chr8 + 143878409 143878409 143878409 CCGCACCCGCCGCACCTGCCCGCACCCGCCGCACCCGCCGCACCCGCCGCACCCGCCGCACCTGC CCGCACCCGCCGCACCTGCCCGCACCCGCCGCCCCCGCCGCACCCGCCGCACCCGCCGCACCTGC A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143878226..143878475 26863196 MeRIP-seq:(Medium) rs1206025345 Functional Loss SNV dbSNP153 33..33 33 - - - 64761 RMVar_ID_64761 Human_SNP_ID_386111552 m1A Human chr8 + 143916100 143916100 143916100 CTTTAGGCACCACTTGGGAGGAAGACACCTTTAAGCGTTGAAAACGGCCCCCGCGCCTCGGTGGG CTTTAGGCACCACTTGGGAGGAAGACACCTTTGAGCGTTGAAAACGGCCCCCGCGCCTCGGTGGG A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143916076..143916100 26863196 MeRIP-seq:(Medium) rs1229094252 Functional Loss SNV dbSNP153 33..33 33 - - - 64762 RMVar_ID_64762 Human_SNP_ID_386111591 m1A Human chr8 - 143916162 143916162 143916162 GAGTCTGCCGTGGCCTGAGGCTGCCTGCGCCCACCCCGCTCTGCATGCGGCCCAGCCCGGCTCCC GAGTCTGCCGTGGCCTGAGGCTGCCTGCGCCCGCCCCGCTCTGCATGCGGCCCAGCCCGGCTCCC T C PLEC Ensembl:ENSG00000178209 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143916111..143916447 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5534374,Human_RBP_ID_9338477,Human_RBP_ID_22465036,Human_RBP_ID_27536609 Human_miRNA_ID_2873187,Human_miRNA_ID_2981150 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64763 RMVar_ID_64763 Human_SNP_ID_386111592 m1A Human chr8 - 143916162 143916162 143916162 GAGTCTGCCGTGGCCTGAGGCTGCCTGCGCCCACCCCGCTCTGCATGCGGCCCAGCCCGGCTCCC GAGTCTGCCGTGGCCTGAGGCTGCCTGCGCCCCCCCCGCTCTGCATGCGGCCCAGCCCGGCTCCC T G PLEC Ensembl:ENSG00000178209 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143916111..143916447 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5534374,Human_RBP_ID_9338477,Human_RBP_ID_22465036,Human_RBP_ID_27536609 Human_miRNA_ID_2873187,Human_miRNA_ID_2981150 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64764 RMVar_ID_64764 Human_SNP_ID_386111809 m1A Human chr8 - 143916451 143916448 143916451 TAAGGACGCGCTGGACCGCAGCATGGTGGAGGAGGGCACGGGGCTGCGGCTGCTGGAGGCTGCCG TAAGGACGCGCTGGACCGCAGCATGGTGGAGG___GCACGGGGCTGCGGCTGCTGGAGGCTGCCG CCCT C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143916426..143916450 26863196 MeRIP-seq:(Medium) rs1563919207 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_89126,Human_RBP_ID_255055,Human_RBP_ID_796017,Human_RBP_ID_845848,Human_RBP_ID_5534376,Human_RBP_ID_22465325,Human_RBP_ID_27363788,Human_RBP_ID_27536616 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64765 RMVar_ID_64765 Human_SNP_ID_386111979 m1A Human chr8 - 143916772 143916772 143916772 CCTGGTGGACAAGATCATGGTGGACCGCATCAACCTGGCCCAGAAGGCCTTCTGCGGCTTCGAGG CCTGGTGGACAAGATCATGGTGGACCGCATCATCCTGGCCCAGAAGGCCTTCTGCGGCTTCGAGG T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143916721..143916840 26863196 MeRIP-seq:(Medium) rs781873281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628766,Human_RBP_ID_27363792 Human_miRNA_ID_1965829,Human_miRNA_ID_2361285,Human_miRNA_ID_2662001,Human_miRNA_ID_2680451 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64766 RMVar_ID_64766 Human_SNP_ID_386111980 m1A Human chr8 - 143916772 143916772 143916772 CCTGGTGGACAAGATCATGGTGGACCGCATCAACCTGGCCCAGAAGGCCTTCTGCGGCTTCGAGG CCTGGTGGACAAGATCATGGTGGACCGCATCAGCCTGGCCCAGAAGGCCTTCTGCGGCTTCGAGG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143916721..143916840 26863196 MeRIP-seq:(Medium) rs781873281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628766,Human_RBP_ID_27363792 Human_miRNA_ID_1965829,Human_miRNA_ID_2361285,Human_miRNA_ID_2662001,Human_miRNA_ID_2680451 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64767 RMVar_ID_64767 Human_SNP_ID_386112072 m1A Human chr8 - 143916974 143916974 143916974 ACCCCACTGAGGAGACGGGCCCCGTGGCTGGCATCCTGGACACGGAGACGCTGGAGAAGGTGTCC ACCCCACTGAGGAGACGGGCCCCGTGGCTGGCGTCCTGGACACGGAGACGCTGGAGAAGGTGTCC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143916924..143917110 26863196 MeRIP-seq:(Medium) rs1169301486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89128,Human_RBP_ID_5430287,Human_RBP_ID_8917280,Human_RBP_ID_22465327,Human_RBP_ID_27161937,Human_RBP_ID_27536625,Human_RBP_ID_27569696 Human_miRNA_ID_2397491,Human_miRNA_ID_2464837 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64768 RMVar_ID_64768 Human_SNP_ID_386112090 m1A Human chr8 + 143917016 143917016 143917016 GGGGCCCGTCTCCTCAGTGGGGTCTGACCAGGAGGCCAGCTGGGTCCTGGAGACGGCGGGGCTGA GGGGCCCGTCTCCTCAGTGGGGTCTGACCAGGGGGCCAGCTGGGTCCTGGAGACGGCGGGGCTGA A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143917001..143917025 26863196 MeRIP-seq:(Medium) rs980115202 Functional Loss SNV dbSNP153 33..33 33 - - - 64769 RMVar_ID_64769 Human_SNP_ID_386112222 m1A Human chr8 - 143917238 143917238 143917238 CCTCCTCGGACGGCGTGGTCAAGTCCATGATCATCGACCGCCGCTCCGGGCGCCAGTACGACATC CCTCCTCGGACGGCGTGGTCAAGTCCATGATCGTCGACCGCCGCTCCGGGCGCCAGTACGACATC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143917126..143917625 32194978 MeRIP-seq:(Medium) rs782326386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8682928 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64770 RMVar_ID_64770 Human_SNP_ID_386112387 m1A Human chr8 + 143917571 143917571 143917571 GTTAGGGTCAAAGAAGCCCTTGGTGTCGTCCGAGGGGTCGGTCAGGATCTCGTTCATCTCCTCAT GTTAGGGTCAAAGAAGCCCTTGGTGTCGTCCGGGGGGTCGGTCAGGATCTCGTTCATCTCCTCAT A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143917523..143917614 26863196 MeRIP-seq:(Medium) rs201073959 Functional Loss SNV dbSNP153 33..33 33 - - - 64771 RMVar_ID_64771 Human_SNP_ID_386112586 m1A Human chr8 + 143917975 143917975 143917975 GGCGGATGATGCCCTTCTTCATGGCCTGGTACACCGAGAGCCGTTCCTTGGTGGCGTCCACGAAG GGCGGATGATGCCCTTCTTCATGGCCTGGTACGCCGAGAGCCGTTCCTTGGTGGCGTCCACGAAG A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143917926..143918000 26863196 MeRIP-seq:(Medium) rs782423006 Functional Loss SNV dbSNP153 33..33 33 - - - 64772 RMVar_ID_64772 Human_SNP_ID_386113279 m1A Human chr8 - 143919123 143919123 143919123 CAGGTGTACACTGAGGAGGAGACAAGAAGGGCATTTGAAGAGACACAGATCGACATTCCCGGCGG CAGGTGTACACTGAGGAGGAGACAAGAAGGGCGTTTGAAGAGACACAGATCGACATTCCCGGCGG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143919076..143919275 26863196 MeRIP-seq:(Medium) rs1554677209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89136,Human_RBP_ID_5628780,Human_RBP_ID_9264190,Human_RBP_ID_9313674,Human_RBP_ID_24537254 Human_miRNA_ID_1939763,Human_miRNA_ID_2496251,Human_miRNA_ID_2497477,Human_miRNA_ID_3082182 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64773 RMVar_ID_64773 Human_SNP_ID_386113288 m1A Human chr8 - 143919142 143919142 143919142 TGAGGTGGTGGAGACCACGCAGGTGTACACTGAGGAGGAGACAAGAAGGGCATTTGAAGAGACAC TGAGGTGGTGGAGACCACGCAGGTGTACACTGGGGAGGAGACAAGAAGGGCATTTGAAGAGACAC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr8:143918864..143919275;chr8:143919076..143919275 26863196 MeRIP-seq:(Medium) rs1554677246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89136,Human_RBP_ID_8923289,Human_RBP_ID_9264190,Human_RBP_ID_9313674,Human_RBP_ID_18114049,Human_RBP_ID_27569704 Human_miRNA_ID_1939763 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64774 RMVar_ID_64774 Human_SNP_ID_386113430 m1A Human chr8 - 143919352 143919352 143919352 CAGCCACCGCGTGCCTGTGGACGTGGCCTACCAGCGCGGCTACTTCAGTGAGGAGATGAACCGCG CAGCCACCGCGTGCCTGTGGACGTGGCCTACCCGCGCGGCTACTTCAGTGAGGAGATGAACCGCG T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143919051..143919645 26863196 MeRIP-seq:(Medium) rs371479882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89137,Human_RBP_ID_8917300,Human_RBP_ID_26832476 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64775 RMVar_ID_64775 Human_SNP_ID_386113804 m1A Human chr8 - 143919989 143919989 143919989 GGCAGGAGCTGTTGCGTCAGTTCCGCACGGGCAAGGTCACCGTGGAGAAGGTCATCAAGATTCTC GGCAGGAGCTGTTGCGTCAGTTCCGCACGGGCGAGGTCACCGTGGAGAAGGTCATCAAGATTCTC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143919940..143920169 26863196 MeRIP-seq:(Medium) rs1554680143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4974358 Human_miRNA_ID_1544239,Human_miRNA_ID_1596972,Human_miRNA_ID_2402228 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64776 RMVar_ID_64776 Human_SNP_ID_386113866 m1A Human chr8 + 143920093 143920093 143920093 ACACCGTCACCGTCCTGCCCTTGAAGCCACCCACGGGGACCTCAACCGGGGTCTTTTCAAAGGTC ACACCGTCACCGTCCTGCCCTTGAAGCCACCCCCGGGGACCTCAACCGGGGTCTTTTCAAAGGTC A C RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143920051..143920125 26863196 MeRIP-seq:(Medium) rs782176923 Functional Loss SNV dbSNP153 33..33 33 - - - 64777 RMVar_ID_64777 Human_SNP_ID_386114243 m1A Human chr8 - 143920645 143920645 143920645 GCTGCCATCCGACATGGCCGTGGCCCTGTTGGAAGCCCAGGCCGGCACCGGGCACATCATCGACC GCTGCCATCCGACATGGCCGTGGCCCTGTTGGGAGCCCAGGCCGGCACCGGGCACATCATCGACC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143920610..143920825 26863196 MeRIP-seq:(Medium) rs1554682501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996720,Human_RBP_ID_5534393,Human_RBP_ID_8923653,Human_RBP_ID_22465333,Human_RBP_ID_26359464 Human_miRNA_ID_2553677 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64778 RMVar_ID_64778 Human_SNP_ID_386114452 m1A Human chr8 - 143920949 143920949 143920949 CGGGCCGGATCACAGTGGAGAAGATCATCAAGATCATCATCACGGTGGTGGAGGAGCAGGAGCAG CGGGCCGGATCACAGTGGAGAAGATCATCAAGTTCATCATCACGGTGGTGGAGGAGCAGGAGCAG T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143920899..143921250 26863196 MeRIP-seq:(Medium) rs782699278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8682940 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64779 RMVar_ID_64779 Human_SNP_ID_386114453 m1A Human chr8 - 143920949 143920949 143920949 CGGGCCGGATCACAGTGGAGAAGATCATCAAGATCATCATCACGGTGGTGGAGGAGCAGGAGCAG CGGGCCGGATCACAGTGGAGAAGATCATCAAGGTCATCATCACGGTGGTGGAGGAGCAGGAGCAG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143920899..143921250 26863196 MeRIP-seq:(Medium) rs782699278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8682940 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64780 RMVar_ID_64780 Human_SNP_ID_386114732 m1A Human chr8 + 143921376 143921376 143921376 ACGGGCACGCGGTGGCTGTGCACGGGGTCGATAACGCCGCCCGTGGCGATCTGGGCCTCCAGCAG ACGGGCACGCGGTGGCTGTGCACGGGGTCGATGACGCCGCCCGTGGCGATCTGGGCCTCCAGCAG A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143921176..143921575 26863196 MeRIP-seq:(Medium) rs371421350 Functional Loss SNV dbSNP153 33..33 33 - - - 64781 RMVar_ID_64781 Human_SNP_ID_386114733 m1A Human chr8 + 143921376 143921376 143921376 ACGGGCACGCGGTGGCTGTGCACGGGGTCGATAACGCCGCCCGTGGCGATCTGGGCCTCCAGCAG ACGGGCACGCGGTGGCTGTGCACGGGGTCGATTACGCCGCCCGTGGCGATCTGGGCCTCCAGCAG A T RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143921176..143921575 26863196 MeRIP-seq:(Medium) rs371421350 Functional Loss SNV dbSNP153 33..33 33 - - - 64782 RMVar_ID_64782 Human_SNP_ID_386114927 m1A Human chr8 - 143921701 143921701 143921701 CAGTATCGCAGGGCTGTTGCTGAAGGCCACCAATGAGAAGCTGAGTGTTTACGCCGCCCTGCAGA CAGTATCGCAGGGCTGTTGCTGAAGGCCACCAGTGAGAAGCTGAGTGTTTACGCCGCCCTGCAGA T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143921651..143921850 26863196 MeRIP-seq:(Medium) rs782802158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179909 Human_miRNA_ID_2337254,Human_miRNA_ID_2339486,Human_miRNA_ID_2341722 Clinvar_Rec_253 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64783 RMVar_ID_64783 Human_SNP_ID_386115182 m1A Human chr8 + 143922094 143922082 143922094 GCAGCTCCTCCTGCTGCCGCCGCTGCTGCTCCAGCTGCTGCAGCTCCTCCTGCTTGCGCCGCACG GCAGCTCCTCCTGCTGCCGCC____________GCTGCTGCAGCTCCTCCTGCTTGCGCCGCACG CGCTGCTGCTCCA C RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143922043..143922226 26863196 MeRIP-seq:(Medium) rs1457330030 Functional Loss DEL dbSNP153 22..33 33 - - - 64784 RMVar_ID_64784 Human_SNP_ID_386115190 m1A Human chr8 + 143922094 143922094 143922094 GCAGCTCCTCCTGCTGCCGCCGCTGCTGCTCCAGCTGCTGCAGCTCCTCCTGCTTGCGCCGCACG GCAGCTCCTCCTGCTGCCGCCGCTGCTGCTCCTGCTGCTGCAGCTCCTCCTGCTTGCGCCGCACG A T RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143922043..143922226 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 64785 RMVar_ID_64785 Human_SNP_ID_386115225 m1A Human chr8 - 143922145 143922145 143922145 GGTGGCCAGCATGGAGGAGGCGCGGCGGCGGCAGCATGAGGCCGAGGAGGGCGTGCGGCGCAAGC GGTGGCCAGCATGGAGGAGGCGCGGCGGCGGCGGCATGAGGCCGAGGAGGGCGTGCGGCGCAAGC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:143921362..143922327;chr8:143921076..143922304;chr8:143921326..143922400;chr8:143921462..143922400 26863196 MeRIP-seq:(Medium) rs1438756624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89147,Human_RBP_ID_5307871,Human_RBP_ID_5534401,Human_RBP_ID_18472624,Human_RBP_ID_23120807 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64786 RMVar_ID_64786 Human_SNP_ID_386115236 m1A Human chr8 - 143922160 143922160 143922160 GGAACGGCAGCGGCTGGTGGCCAGCATGGAGGAGGCGCGGCGGCGGCAGCATGAGGCCGAGGAGG GGAACGGCAGCGGCTGGTGGCCAGCATGGAGGCGGCGCGGCGGCGGCAGCATGAGGCCGAGGAGG T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143921926..143922325 26863196 MeRIP-seq:(Medium) rs1488549704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89147,Human_RBP_ID_845914,Human_RBP_ID_5534401,Human_RBP_ID_18472624,Human_RBP_ID_23120807 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64787 RMVar_ID_64787 Human_SNP_ID_386115299 m1A Human chr8 - 143922240 143922240 143922240 GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCACAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCTCAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143921726..143922300 26863196 MeRIP-seq:(Medium) rs11778026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89147,Human_RBP_ID_5154354,Human_RBP_ID_5534402,Human_RBP_ID_18472624,Human_RBP_ID_24549426,Human_RBP_ID_26359469 GWAS_ID_7884 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64788 RMVar_ID_64788 Human_SNP_ID_386115300 m1A Human chr8 - 143922240 143922240 143922240 GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCACAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCCCAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143921726..143922300 26863196 MeRIP-seq:(Medium) rs11778026 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_89147,Human_RBP_ID_5154354,Human_RBP_ID_5534402,Human_RBP_ID_18472624,Human_RBP_ID_24549426,Human_RBP_ID_26359469 GWAS_ID_7884 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 64789 RMVar_ID_64789 Human_SNP_ID_386115605 m1A Human chr8 - 143922703 143922703 143922703 CGCTGAGGAGGACGCCCAGCGCTTCCGGAAGCAGGCGGAGGAGATCGGTGAGAAGCTGCACCGCA CGCTGAGGAGGACGCCCAGCGCTTCCGGAAGCTGGCGGAGGAGATCGGTGAGAAGCTGCACCGCA T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143922701..143922725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_8923313,Human_RBP_ID_9314127 Human_miRNA_ID_207161,Human_miRNA_ID_1490930 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64790 RMVar_ID_64790 Human_SNP_ID_386115705 m1A Human chr8 - 143922848 143922848 143922848 AGGAGCAGATGGCGCAGCAGCTGGCGGAGGAGACGCAGGGCTTCCAGCGGACGCTGGAGGCCGAG AGGAGCAGATGGCGCAGCAGCTGGCGGAGGAGGCGCAGGGCTTCCAGCGGACGCTGGAGGCCGAG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143922826..143922850 26863196 MeRIP-seq:(Medium) rs1564011174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89150,Human_RBP_ID_796025,Human_RBP_ID_4974407,Human_RBP_ID_9405862,Human_RBP_ID_18125498,Human_RBP_ID_22731718,Human_RBP_ID_23087988,Human_RBP_ID_26359472 Human_miRNA_ID_3023663 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64791 RMVar_ID_64791 Human_SNP_ID_386115735 m1A Human chr8 - 143922889 143922889 143922889 GGAGCTTGCGCAGGAGCAGGCGCGGCGGCTGCAGGAGGACAAGGAGCAGATGGCGCAGCAGCTGG GGAGCTTGCGCAGGAGCAGGCGCGGCGGCTGCGGGAGGACAAGGAGCAGATGGCGCAGCAGCTGG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143922876..143922900 26863196 MeRIP-seq:(Medium) rs782728921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89150,Human_RBP_ID_5628797,Human_RBP_ID_22732073 Human_miRNA_ID_2254703 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64792 RMVar_ID_64792 Human_SNP_ID_386116712 m1A Human chr8 - 143924183 143924183 143924183 AGCTGGAGCGGCAGAAGGGGCTGGTGGAGGACACGCTGAGGCAGCGGCGGCAGGTGGAGGAGGAG AGCTGGAGCGGCAGAAGGGGCTGGTGGAGGACGCGCTGAGGCAGCGGCGGCAGGTGGAGGAGGAG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:143924140..143924283 26863196 MeRIP-seq:(Medium) rs782429508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89151,Human_RBP_ID_5514544,Human_RBP_ID_22731721,Human_RBP_ID_24549530,Human_RBP_ID_27574632 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64793 RMVar_ID_64793 Human_SNP_ID_386116787 m1A Human chr8 - 143924302 143924299 143924302 CCTGCGGCGGCTGGCGGAGGACGAGGCCTTCCAGCGGCGGCGGCTGGAGGAGCAGGCCGCGCAAC CCTGCGGCGGCTGGCGGAGGACGAGGCCTTCC___GGCGGCGGCTGGAGGAGCAGGCCGCGCAAC CGCT C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr8:143922721..143927675;chr8:143922738..143927575;chr8:143923558..143924475 26863196 MeRIP-seq:(Medium) rs781787562 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_89151,Human_RBP_ID_5534415,Human_RBP_ID_23120808,Human_RBP_ID_27831623 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64794 RMVar_ID_64794 Human_SNP_ID_386117095 m1A Human chr8 - 143924725 143924723 143924726 GGGGGAGCAGCAGCGGCAGCTGCTGGAGGAGGAGCTGGCCCGGCTGCAGCGTGAGGCGGCTGCAG GGGGGAGCAGCAGCGGCAGCTGCTGGAGGAG___CTGGCCCGGCTGCAGCGTGAGGCGGCTGCAG GCTC G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143924676..143924750 26863196 MeRIP-seq:(Medium) rs1554698788 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_89153,Human_RBP_ID_5534418,Human_RBP_ID_9313695,Human_RBP_ID_18472550,Human_RBP_ID_22115225,Human_RBP_ID_22731724,Human_RBP_ID_24555256,Human_RBP_ID_26359483,Human_RBP_ID_27536739,Human_RBP_ID_27831625 Human_miRNA_ID_2662002,Human_miRNA_ID_2680452 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64795 RMVar_ID_64795 Human_SNP_ID_386117133 m1A Human chr8 - 143924791 143924791 143924791 AGGCACCGCGCAGCAGCGCCTGGCCGCGGAGCAGGAGTTGATCCGGCTGCGGGCCGAGACGGAGC AGGCACCGCGCAGCAGCGCCTGGCCGCGGAGCGGGAGTTGATCCGGCTGCGGGCCGAGACGGAGC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143924776..143924800 26863196 MeRIP-seq:(Medium) rs781989571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89153 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64796 RMVar_ID_64796 Human_SNP_ID_386117210 m1A Human chr8 - 143924896 143924896 143924896 GGAGGCGGAGCGCGAGGCGCGGCGGCGCGGCAAGGCGGAGGAGCAGGCCGTCCGGCAGCGGGAGC GGAGGCGGAGCGCGAGGCGCGGCGGCGCGGCAGGGCGGAGGAGCAGGCCGTCCGGCAGCGGGAGC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143924845..143925100 26863196 MeRIP-seq:(Medium) rs782459426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89153,Human_RBP_ID_255061,Human_RBP_ID_796030,Human_RBP_ID_845916,Human_RBP_ID_959520,Human_RBP_ID_5534420,Human_RBP_ID_18472552,Human_RBP_ID_24549531,Human_RBP_ID_26359485 Clinvar_Rec_254 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 64797 RMVar_ID_64797 Human_SNP_ID_386118335 m1A Human chr8 - 143926798 143926798 143926798 ACATCAAGTTCATCAGCGAGACTCTGCGGCGCATGGAGGAGGAGGAGGTACAGCCCGTTGGGCGG ACATCAAGTTCATCAGCGAGACTCTGCGGCGCGTGGAGGAGGAGGAGGTACAGCCCGTTGGGCGG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143926776..143926825 26863196 MeRIP-seq:(Medium) rs782208072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628821,Human_RBP_ID_8917325,Human_RBP_ID_26360250 Human_Splice_Rec_1021396,Human_Splice_Rec_1021397,Human_Splice_Rec_1021456,Human_Splice_Rec_1021457,Human_Splice_Rec_1021516,Human_Splice_Rec_1021517,Human_Splice_Rec_1021576,Human_Splice_Rec_1021577,Human_Splice_Rec_1021636,Human_Splice_Rec_1021637,Human_Splice_Rec_1021696,Human_Splice_Rec_1021697,Human_Splice_Rec_1021756,Human_Splice_Rec_1021757,Human_Splice_Rec_1021816,Human_Splice_Rec_1021817,Human_Splice_Rec_1021876,Human_Splice_Rec_1021877,Human_Splice_Rec_1021934,Human_Splice_Rec_1021935 Human_miRNA_ID_2896542,Human_miRNA_ID_2896543 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_348791,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_303535,RMVar_hsa_circ_99901,RMVar_hsa_circ_105338,RMVar_hsa_circ_105904,RMVar_hsa_circ_103649,RMVar_hsa_circ_81411,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254978,RMVar_hsa_circ_254980,RMVar_hsa_circ_19073,RMVar_hsa_circ_254981,RMVar_hsa_circ_254979,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_254971 64798 RMVar_ID_64798 Human_SNP_ID_386118508 m1A Human chr8 - 143927080 143927080 143927080 GCTGGTGGCTGACCGCAGTGCATTGCCACAGGACTATGAACTCCAGCTGGTGACGTACAAGGCGC GCTGGTGGCTGACCGCAGTGCATTGCCACAGGGCTATGAACTCCAGCTGGTGACGTACAAGGCGC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143927051..143927125 26863196 MeRIP-seq:(Medium) rs782382295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974198,Human_RBP_ID_5405048,Human_RBP_ID_22555606,Human_RBP_ID_22688611,Human_RBP_ID_26359493 Human_Splice_Rec_1021394,Human_Splice_Rec_1021454,Human_Splice_Rec_1021514,Human_Splice_Rec_1021574,Human_Splice_Rec_1021634,Human_Splice_Rec_1021694,Human_Splice_Rec_1021754,Human_Splice_Rec_1021814,Human_Splice_Rec_1021874,Human_Splice_Rec_1021932 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_348791,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_303535,RMVar_hsa_circ_99901,RMVar_hsa_circ_105338,RMVar_hsa_circ_105904,RMVar_hsa_circ_103649,RMVar_hsa_circ_81411,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254978,RMVar_hsa_circ_254980,RMVar_hsa_circ_19073,RMVar_hsa_circ_254981,RMVar_hsa_circ_254979,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_254971 64799 RMVar_ID_64799 Human_SNP_ID_386118610 m1A Human chr8 - 143927286 143927286 143927286 CGAGCGCCACGGCGAGAAGGTCGAGGAGTGCCAGAGGTTTGCGAAACAGTACATCAACGCCATCA CGAGCGCCACGGCGAGAAGGTCGAGGAGTGCCGGAGGTTTGCGAAACAGTACATCAACGCCATCA T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143926976..143927625 26863196 MeRIP-seq:(Medium) rs1304169541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89160,Human_RBP_ID_3973430,Human_RBP_ID_8682944,Human_RBP_ID_18125143,Human_RBP_ID_19140489,Human_RBP_ID_26359494,Human_RBP_ID_27832216 Human_Splice_Rec_1021392,Human_Splice_Rec_1021393,Human_Splice_Rec_1021452,Human_Splice_Rec_1021453,Human_Splice_Rec_1021512,Human_Splice_Rec_1021513,Human_Splice_Rec_1021572,Human_Splice_Rec_1021573,Human_Splice_Rec_1021632,Human_Splice_Rec_1021633,Human_Splice_Rec_1021692,Human_Splice_Rec_1021693,Human_Splice_Rec_1021752,Human_Splice_Rec_1021753,Human_Splice_Rec_1021812,Human_Splice_Rec_1021813,Human_Splice_Rec_1021872,Human_Splice_Rec_1021873,Human_Splice_Rec_1021930,Human_Splice_Rec_1021931 Human_miRNA_ID_2647734,Human_miRNA_ID_2647735,Human_miRNA_ID_2670331,Human_miRNA_ID_2670332,Human_miRNA_ID_3100983,Human_miRNA_ID_3100984 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_348791,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105338,RMVar_hsa_circ_105904,RMVar_hsa_circ_103649,RMVar_hsa_circ_81411,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254978,RMVar_hsa_circ_254980,RMVar_hsa_circ_19073,RMVar_hsa_circ_254979,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_254971 64800 RMVar_ID_64800 Human_SNP_ID_386118857 m1A Human chr8 - 143927654 143927654 143927654 GGAGCGACTGCAGCAGCGGCACGGGGAGCGGGACGTGGAGGTGGAGCGCTGGCGGGAGCGGGTCG GGAGCGACTGCAGCAGCGGCACGGGGAGCGGGGCGTGGAGGTGGAGCGCTGGCGGGAGCGGGTCG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143927226..143927764 26863196 MeRIP-seq:(Medium) rs1358915562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89162,Human_RBP_ID_255063,Human_RBP_ID_957928,Human_RBP_ID_3973432,Human_RBP_ID_5406884,Human_RBP_ID_5534429,Human_RBP_ID_5628825,Human_RBP_ID_8923325,Human_RBP_ID_9313700,Human_RBP_ID_9441551,Human_RBP_ID_17672384,Human_RBP_ID_18472554,Human_RBP_ID_19023216,Human_RBP_ID_22465339,Human_RBP_ID_22534443,Human_RBP_ID_22627256,Human_RBP_ID_26359495,Human_RBP_ID_27843362 Human_miRNA_ID_209267,Human_miRNA_ID_2015756,Human_miRNA_ID_2015757 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_348791,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105338,RMVar_hsa_circ_105904,RMVar_hsa_circ_103649,RMVar_hsa_circ_81411,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254978,RMVar_hsa_circ_254980,RMVar_hsa_circ_254979,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254983,RMVar_hsa_circ_254982 64801 RMVar_ID_64801 Human_SNP_ID_386118910 m1A Human chr8 + 143927730 143927730 143927730 TGCCCCCCGCAGCTCATCCCGCAGGGCGTCGAACGTGGGCTGCTGTGCCTCGGCCTGGGCCCGCA TGCCCCCCGCAGCTCATCCCGCAGGGCGTCGATCGTGGGCTGCTGTGCCTCGGCCTGGGCCCGCA A T RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:143927576..143927775 26863196 MeRIP-seq:(Medium) rs1554708450 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_255 64802 RMVar_ID_64802 Human_SNP_ID_386118988 m1A Human chr8 + 143927858 143927857 143927859 CCATGAAGCCCAAGCCTCGAAACGATACCTTCAGAGAGGCCTTGGTGGCCTCGAGCTCCGGGAGG CCATGAAGCCCAAGCCTCGAAACGATACCTTC__AGAGGCCTTGGTGGCCTCGAGCTCCGGGAGG CAG C RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143927851..143927942 26863196 MeRIP-seq:(Medium) rs782622948 Functional Loss DEL dbSNP153 33..34 33 - - - 64803 RMVar_ID_64803 Human_SNP_ID_386120020 m1A Human chr8 - 143929959 143929959 143929959 CCTGGCAGAGCCTTCGCCGCGACGTGCAGCTCATCCGCTCCTGGTCCCTGGCCACGGTACGCCTG CCTGGCAGAGCCTTCGCCGCGACGTGCAGCTCCTCCGCTCCTGGTCCCTGGCCACGGTACGCCTG T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143929940..143930093 26863196 MeRIP-seq:(Medium) rs1210721750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179912,Human_RBP_ID_18472555 Human_Splice_Rec_1021383,Human_Splice_Rec_1021443,Human_Splice_Rec_1021503,Human_Splice_Rec_1021563,Human_Splice_Rec_1021623,Human_Splice_Rec_1021683,Human_Splice_Rec_1021743,Human_Splice_Rec_1021803,Human_Splice_Rec_1021863,Human_Splice_Rec_1021921 Human_miRNA_ID_2894022,Human_miRNA_ID_2894023,Human_miRNA_ID_2993267,Human_miRNA_ID_2993268 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_2489 64804 RMVar_ID_64804 Human_SNP_ID_386120579 m1A Human chr8 + 143930948 143930946 143930948 GGCTCTCCCCCCGGCCCAGCCCTGCCGACCTCAGAGGCCATTTCAGTCTCCAGTCCCTCTTCCCT GGCTCTCCCCCCGGCCCAGCCCTGCCGACCT__GAGGCCATTTCAGTCTCCAGTCCCTCTTCCCT TCA T RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143930946..143931025 26863196 MeRIP-seq:(Medium) rs1483889417 Functional Loss DEL dbSNP153 32..33 33 - - - 64805 RMVar_ID_64805 Human_SNP_ID_386120683 m1A Human chr8 - 143931393 143931280 143931393 GAGGCACCATGGGAGGTGTAGAGGTCAGCCGAAGCGGGAATGAGGCAGGATGTTCTGGGCTGCAT GAGGCACCATGGGAGGTGTAGAGGTCAGCCGA_________________________________ CTTGGCTGACCTCTACACCTCCCATGGTGCCTCCCAACTCCTGCTGGCCCCTCCAGTTGCCCCCTAGTCTCCAGAGTACCCATGCAGCCCAGAACATCCTGCCTCATTCCCGCT C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143930670..143931600;chr8:143931176..143931569;chr8:143931122..143931525 26863196 MeRIP-seq:(Medium) rs1564115822 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_89177 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985 64806 RMVar_ID_64806 Human_SNP_ID_386120723 m1A Human chr8 - 143931393 143931393 143931393 GAGGCACCATGGGAGGTGTAGAGGTCAGCCGAAGCGGGAATGAGGCAGGATGTTCTGGGCTGCAT GAGGCACCATGGGAGGTGTAGAGGTCAGCCGAGGCGGGAATGAGGCAGGATGTTCTGGGCTGCAT T C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143930670..143931600;chr8:143931176..143931569;chr8:143931122..143931525 26863196 MeRIP-seq:(Medium) rs6995402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89177 GWAS_ID_7885,GWAS_ID_7886,GWAS_ID_7887,GWAS_ID_7888,GWAS_ID_7889,GWAS_ID_7890,GWAS_ID_7891,GWAS_ID_7892,GWAS_ID_7893 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985 64807 RMVar_ID_64807 Human_SNP_ID_386121176 m1A Human chr8 - 143932195 143932195 143932195 TGCGGGAGCTGGAGCTGAAGGAGAAGAAGATCAAGGAGCTCCAAAATGCTGGGGACCGGCTGCTG TGCGGGAGCTGGAGCTGAAGGAGAAGAAGATCGAGGAGCTCCAAAATGCTGGGGACCGGCTGCTG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143932144..143932248 26863196 MeRIP-seq:(Medium) rs1407260713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89182,Human_RBP_ID_3974209,Human_RBP_ID_5633400,Human_RBP_ID_9406626,Human_RBP_ID_19023221,Human_RBP_ID_27536751 Human_Splice_Rec_1021372,Human_Splice_Rec_1021373,Human_Splice_Rec_1021432,Human_Splice_Rec_1021433,Human_Splice_Rec_1021492,Human_Splice_Rec_1021493,Human_Splice_Rec_1021552,Human_Splice_Rec_1021553,Human_Splice_Rec_1021612,Human_Splice_Rec_1021613,Human_Splice_Rec_1021672,Human_Splice_Rec_1021673,Human_Splice_Rec_1021732,Human_Splice_Rec_1021733,Human_Splice_Rec_1021792,Human_Splice_Rec_1021793,Human_Splice_Rec_1021852,Human_Splice_Rec_1021853,Human_Splice_Rec_1021910,Human_Splice_Rec_1021911 Human_miRNA_ID_2441224,Human_miRNA_ID_2441225 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985 64808 RMVar_ID_64808 Human_SNP_ID_386121287 m1A Human chr8 + 143932425 143932425 143932425 CGCTCACCGAGTAGCTCTCCTTCTTGGCGGTCATGTTGGTGTTGCGGTCGCTCCAGTCGAAGCCC CGCTCACCGAGTAGCTCTCCTTCTTGGCGGTCGTGTTGGTGTTGCGGTCGCTCCAGTCGAAGCCC A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143932393..143933173 26863196 MeRIP-seq:(Medium) rs1260484783 Functional Loss SNV dbSNP153 33..33 33 - - - 64809 RMVar_ID_64809 Human_SNP_ID_386121291 m1A Human chr8 - 143932440 143932435 143932441 GGAGGAGGAGGAGGTGGGCTTCGACTGGAGCGACCGCAACACCAACATGACCGCCAAGAAGGAGA GGAGGAGGAGGAGGTGGGCTTCGACTGGAGC______AACACCAACATGACCGCCAAGAAGGAGA TGCGGTC T PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143932401..143932500 26863196 MeRIP-seq:(Medium) rs1244615297 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_958289,Human_RBP_ID_3973442,Human_RBP_ID_8923333,Human_RBP_ID_9313703,Human_RBP_ID_23316005,Human_RBP_ID_24549428,Human_RBP_ID_26360256 Human_Splice_Rec_1021371,Human_Splice_Rec_1021431,Human_Splice_Rec_1021491,Human_Splice_Rec_1021551,Human_Splice_Rec_1021611,Human_Splice_Rec_1021671,Human_Splice_Rec_1021731,Human_Splice_Rec_1021791,Human_Splice_Rec_1021851,Human_Splice_Rec_1021909 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985 64810 RMVar_ID_64810 Human_SNP_ID_386121403 m1A Human chr8 - 143932599 143932599 143932599 AGTGGGGGCAGGGCCAGCCGGGGGAGGTGGGTAGCCCGCGGCCTGCTGACACGCACCCTCCTGCC AGTGGGGGCAGGGCCAGCCGGGGGAGGTGGGTGGCCCGCGGCCTGCTGACACGCACCCTCCTGCC T C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143932589..143932678 26863196 MeRIP-seq:(Medium) rs201550913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5405063,Human_RBP_ID_19141936,Human_RBP_ID_22625835,Human_RBP_ID_22689738 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985 64811 RMVar_ID_64811 Human_SNP_ID_386121602 m1A Human chr8 - 143932926 143932926 143932926 CCTGCAGGACCTGCTGGCCTGGGTGGAGGAGAACCAGCACCGTGTGGATGGCGCTGAGTGGGGTG CCTGCAGGACCTGCTGGCCTGGGTGGAGGAGAGCCAGCACCGTGTGGATGGCGCTGAGTGGGGTG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:143932801..143932975 26863196 MeRIP-seq:(Medium) rs1554718436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_254972,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_22489,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985,RMVar_hsa_circ_99232,RMVar_hsa_circ_121074,RMVar_hsa_circ_254988,RMVar_hsa_circ_54722,RMVar_hsa_circ_254987 64812 RMVar_ID_64812 Human_SNP_ID_386122336 m1A Human chr8 - 143934384 143934382 143934385 GCCCCCTGGCTACCACCCGCTGGATGTGGAGAAGGAGTGGGGCAAGCTGCACGTGGCCATCCTGG GCCCCCTGGCTACCACCCGCTGGATGTGGAG___GAGTGGGGCAAGCTGCACGTGGCCATCCTGG CCTT C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143934376..143934400 26863196 MeRIP-seq:(Medium) rs782613887 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22465038 Human_Splice_Rec_1021360,Human_Splice_Rec_1021361,Human_Splice_Rec_1021420,Human_Splice_Rec_1021421,Human_Splice_Rec_1021480,Human_Splice_Rec_1021481,Human_Splice_Rec_1021540,Human_Splice_Rec_1021541,Human_Splice_Rec_1021600,Human_Splice_Rec_1021601,Human_Splice_Rec_1021660,Human_Splice_Rec_1021661,Human_Splice_Rec_1021720,Human_Splice_Rec_1021721,Human_Splice_Rec_1021780,Human_Splice_Rec_1021781,Human_Splice_Rec_1021840,Human_Splice_Rec_1021841,Human_Splice_Rec_1021898,Human_Splice_Rec_1021899,Human_Splice_Rec_1021962,Human_Splice_Rec_1021963 Human_miRNA_ID_207166,Human_miRNA_ID_1490935,Human_miRNA_ID_2012517,Human_miRNA_ID_2012518,Human_miRNA_ID_2708427,Human_miRNA_ID_2708428,Human_miRNA_ID_2758893,Human_miRNA_ID_2758894 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_85553,RMVar_hsa_circ_3035,RMVar_hsa_circ_254972,RMVar_hsa_circ_254974,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985,RMVar_hsa_circ_99232,RMVar_hsa_circ_121074,RMVar_hsa_circ_254988,RMVar_hsa_circ_254987,RMVar_hsa_circ_10998,RMVar_hsa_circ_57497,RMVar_hsa_circ_108803,RMVar_hsa_circ_108144,RMVar_hsa_circ_254989,RMVar_hsa_circ_254991,RMVar_hsa_circ_96142,RMVar_hsa_circ_254990 64813 RMVar_ID_64813 Human_SNP_ID_386124385 m1A Human chr8 + 143939421 143939421 143939421 GGTTGTCCTCCGAGCTGGTTCTCTTTCGGCCCAGGCCCTCGGGCTGCGGCACGCGGAGCTGGTGC GGTTGTCCTCCGAGCTGGTTCTCTTTCGGCCCGGGCCCTCGGGCTGCGGCACGCGGAGCTGGTGC A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143939419..143939598 26863196 MeRIP-seq:(Medium) rs782520654 Functional Loss SNV dbSNP153 33..33 33 - - - 64814 RMVar_ID_64814 Human_SNP_ID_386124397 m1A Human chr8 - 143939433 143939433 143939433 CAGCATGTCTCAGCACCAGCTCCGCGTGCCGCAGCCCGAGGGCCTGGGCCGAAAGAGAACCAGCT CAGCATGTCTCAGCACCAGCTCCGCGTGCCGCTGCCCGAGGGCCTGGGCCGAAAGAGAACCAGCT T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143939431..143939617 26863196 MeRIP-seq:(Medium) rs1554726715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8155114,Human_RBP_ID_8222948 Human_Splice_Rec_1021341 RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 64815 RMVar_ID_64815 Human_SNP_ID_386125477 m1A Human chr8 - 143942482 143942482 143942482 TGTCGGGGGCGGGGGGCGCCTTTGCCTCGCCGAGGGAGGTCTTGCTGGAGCGGCCGTGCTGGCTG TGTCGGGGGCGGGGGGCGCCTTTGCCTCGCCGGGGGAGGTCTTGCTGGAGCGGCCGTGCTGGCTG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143942478..143942605 26863196 MeRIP-seq:(Medium) rs1554729540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885594,Human_RBP_ID_4995258,Human_RBP_ID_5243761,Human_RBP_ID_8155128,Human_RBP_ID_8221611,Human_RBP_ID_18172522,Human_RBP_ID_18506002,Human_RBP_ID_22704561,Human_RBP_ID_22732533 Human_Splice_Rec_1021401 RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 64816 RMVar_ID_64816 Human_SNP_ID_386125889 m1A Human chr8 - 143943775 143943775 143943775 GGGACGTCGGTGGGCGCAGGACGAGCAAGGTAAGCCCCGCTGGTGGCTGCCAGGGACTCGAGGCG GGGACGTCGGTGGGCGCAGGACGAGCAAGGTACGCCCCGCTGGTGGCTGCCAGGGACTCGAGGCG T G PLEC Ensembl:ENSG00000178209 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143943772..143944241 26863196 MeRIP-seq:(Medium) rs377195293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 64817 RMVar_ID_64817 Human_SNP_ID_386127025 m1A Human chr8 + 143946830 143946830 143946830 GTATTTCAGGAGCCAGGCGGGAGCAGAGCCCCAAACTGCCCACCACACCCCACTCCTTGAGACTC GTATTTCAGGAGCCAGGCGGGAGCAGAGCCCCCAACTGCCCACCACACCCCACTCCTTGAGACTC A C RF00017-4575,NONHSAG051524.2,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS00008BC9F8,RNACentral:URS000098982A SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143946828..143947039 26863196 MeRIP-seq:(Medium) rs930000260 Functional Loss SNV dbSNP153 33..33 33 - - - 64818 RMVar_ID_64818 Human_SNP_ID_386127323 m1A Human chr8 + 143947826 143947826 143947826 TATAAAAACACATTCCTACAGCTTCCCACCACACCAAGCAACTGAAACTCTGCCACAGGCCCAGG TATAAAAACACATTCCTACAGCTTCCCACCACGCCAAGCAACTGAAACTCTGCCACAGGCCCAGG A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143947824..143947955 26863196 MeRIP-seq:(Medium) rs1196257369 Functional Loss SNV dbSNP153 33..33 33 - - - 64819 RMVar_ID_64819 Human_SNP_ID_386127331 m1A Human chr8 - 143947862 143947862 143947862 GCCGGAAGGCCAGAGGGAGAGGACCCATGGGAAGGCCCTGGGCCTGTGGCAGAGTTTCAGTTGCT GCCGGAAGGCCAGAGGGAGAGGACCCATGGGACGGCCCTGGGCCTGTGGCAGAGTTTCAGTTGCT T G PLEC Ensembl:ENSG00000178209 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143947857..143948000 26863196 MeRIP-seq:(Medium) rs1348958486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3886514,Human_RBP_ID_8944572 RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 64820 RMVar_ID_64820 Human_SNP_ID_386128091 m1A Human chr8 - 143950253 143950253 143950253 GTCGGAAGGAGCTTGAGGAGGTGTCACCTGAGACCCCTGTGGTGCCTGCTACCACCCAGCGGACC GTCGGAAGGAGCTTGAGGAGGTGTCACCTGAGGCCCCTGTGGTGCCTGCTACCACCCAGCGGACC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143950247..143950423 26863196 MeRIP-seq:(Medium) rs1170535570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3886529,Human_RBP_ID_5329003,Human_RBP_ID_8221651,Human_RBP_ID_18427023,Human_RBP_ID_18466954,Human_RBP_ID_18961279,Human_RBP_ID_22419257,Human_RBP_ID_22732550 Human_Splice_Rec_1021581 RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 64821 RMVar_ID_64821 Human_SNP_ID_386129596 m1A Human chr8 + 143953839 143953839 143953839 CAGGCAGAGTCCAGCCCCGCACCGCACTGCCCAGGCCAGCGCCGCAGCCGGGGGAGGAGCCCGGA CAGGCAGAGTCCAGCCCCGCACCGCACTGCCCGGGCCAGCGCCGCAGCCGGGGGAGGAGCCCGGA A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143953835..143954570 26863196 MeRIP-seq:(Medium) rs544032210 Functional Loss SNV dbSNP153 33..33 33 - - - 64822 RMVar_ID_64822 Human_SNP_ID_386129597 m1A Human chr8 + 143953839 143953839 143953839 CAGGCAGAGTCCAGCCCCGCACCGCACTGCCCAGGCCAGCGCCGCAGCCGGGGGAGGAGCCCGGA CAGGCAGAGTCCAGCCCCGCACCGCACTGCCCTGGCCAGCGCCGCAGCCGGGGGAGGAGCCCGGA A T RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143953835..143954570 26863196 MeRIP-seq:(Medium) rs544032210 Functional Loss SNV dbSNP153 33..33 33 - - - 64823 RMVar_ID_64823 Human_SNP_ID_386130404 m1A Human chr8 - 143956676 143956676 143956676 ACTCACAGGCGGGCAGCTTGACTTCAGGGGGGAAGTTAAAGGCGGAGTCGGTGCATGAAAAGCTG ACTCACAGGCGGGCAGCTTGACTTCAGGGGGGGAGTTAAAGGCGGAGTCGGTGCATGAAAAGCTG T C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143956673..143956795 32194978 MeRIP-seq:(Medium) rs1326626070 Functional Loss SNV dbSNP153 33..33 33 - - - 64824 RMVar_ID_64824 Human_SNP_ID_386132565 m1A Human chr8 + 143965041 143965041 143965041 ACCCTGGTGTGCCCCTGTGGATGGCCTTCCCCACCCTCACCGTCCCACTTGGCCCCAGCCCACCT ACCCTGGTGTGCCCCTGTGGATGGCCTTCCCCGCCCTCACCGTCCCACTTGGCCCCAGCCCACCT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143965039..143965253 26863196 MeRIP-seq:(Medium) rs925130203 Functional Loss SNV dbSNP153 33..33 33 - - - 64825 RMVar_ID_64825 Human_SNP_ID_386132752 m1A Human chr8 + 143965907 143965907 143965907 AGGCCAAGGCCCAGGGAACTCCTTCCCCAGGGAACTCGGGCCAGCATCCAGCTGAGGCTGTGACC AGGCCAAGGCCCAGGGAACTCCTTCCCCAGGGGACTCGGGCCAGCATCCAGCTGAGGCTGTGACC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143965903..143966593 26863196 MeRIP-seq:(Medium) rs564926711 Functional Loss SNV dbSNP153 33..33 33 - - - 64826 RMVar_ID_64826 Human_SNP_ID_386134399 m1A Human chr8 + 143971500 143971500 143971500 GACAGGAAGGGCCGGGGCTCCAGCCCTCTAGCAGGTCCAAGGGGCTCACAGAGGTCAGGCCTGGA GACAGGAAGGGCCGGGGCTCCAGCCCTCTAGCCGGTCCAAGGGGCTCACAGAGGTCAGGCCTGGA A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143971498..143971582 26863196 MeRIP-seq:(Medium) rs1340541601 Functional Loss SNV dbSNP153 33..33 33 - - - 64827 RMVar_ID_64827 Human_SNP_ID_386134910 m1A Human chr8 + 143973336 143973336 143973336 GCTCGGGCCGGCGATCGGGACCGCCACCGTGGACGACAAGGTGCTCGGCGGCTGGGCTGTCAGGA GCTCGGGCCGGCGATCGGGACCGCCACCGTGGGCGACAAGGTGCTCGGCGGCTGGGCTGTCAGGA A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143973334..143973525 26863196 MeRIP-seq:(Medium) rs1490382313 Functional Loss SNV dbSNP153 33..33 33 - - - 64828 RMVar_ID_64828 Human_SNP_ID_386135526 m1A Human chr8 - 143975246 143975246 143975246 GGAACCTTGGGAAAACGCAGCGGAGCCGGCGCAGCGGGGGTGGCGCTGGGAGCAACGGGAGTGTC GGAACCTTGGGAAAACGCAGCGGAGCCGGCGCCGCGGGGGTGGCGCTGGGAGCAACGGGAGTGTC T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr8:143975201..143975363;chr8:143975201..143975300 26863196 MeRIP-seq:(Medium) rs1014833024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1021761,Human_Splice_Rec_1021821,Human_Splice_Rec_1021879,Human_Splice_Rec_1021939,Human_Splice_Rec_1022005 64829 RMVar_ID_64829 Human_SNP_ID_386135542 m1A Human chr8 - 143975266 143975266 143975266 CCCTGGGGACACACTGCCCTGGAACCTTGGGAAAACGCAGCGGAGCCGGCGCAGCGGGGGTGGCG CCCTGGGGACACACTGCCCTGGAACCTTGGGAGAACGCAGCGGAGCCGGCGCAGCGGGGGTGGCG T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143975215..143975721 26863196 MeRIP-seq:(Medium) rs1554745670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1021761,Human_Splice_Rec_1021821,Human_Splice_Rec_1021879,Human_Splice_Rec_1021939,Human_Splice_Rec_1022005 64830 RMVar_ID_64830 Human_SNP_ID_386136342 m1A Human chr8 + 143977789 143977789 143977789 GGGGGGCGAGTAGCGGTCCTGCACCGACAGGGAGGCGCGCCTGGCGAAATACACGCCCTTCCCGT GGGGGGCGAGTAGCGGTCCTGCACCGACAGGGGGGCGCGCCTGGCGAAATACACGCCCTTCCCGT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143977750..143978076 32194978 MeRIP-seq:(Medium) rs1554746630 Functional Loss SNV dbSNP153 33..33 33 - - - 64831 RMVar_ID_64831 Human_SNP_ID_386138505 m1A Human chr8 - 143983693 143983693 143983693 CCTCAGGAGCAGCCAGAGGAGGAGGTGACCCCAGGGCATGAGGAGGAGGAGCCTGTGGCCCCCAG CCTCAGGAGCAGCCAGAGGAGGAGGTGACCCCGGGGCATGAGGAGGAGGAGCCTGTGGCCCCCAG T C PARP10 Ensembl:ENSG00000178685 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143983656..143983797 26863196 MeRIP-seq:(Medium) rs1336744271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8238784,Human_RBP_ID_19022275,Human_RBP_ID_23088064 64832 RMVar_ID_64832 Human_SNP_ID_386138866 m1A Human chr8 - 143984646 143984646 143984646 GGCCTGGTGGAGATGGTGCTATTGATGGAGCCAGGGGCGATGCGCTTCCTGCAGCTCTACCATGA GGCCTGGTGGAGATGGTGCTATTGATGGAGCCGGGGGCGATGCGCTTCCTGCAGCTCTACCATGA T C PARP10 Ensembl:ENSG00000178685 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143984608..143984999 26863196 MeRIP-seq:(Medium) rs1400530620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19023242 64833 RMVar_ID_64833 Human_SNP_ID_386138940 m1A Human chr8 + 143984822 143984822 143984822 GGCAATTTCCACCAGGCCCTCCTGCCCCAGCAACCCCTTAGAGGTCTCCACTGGGCCTGCAGACC GGCAATTTCCACCAGGCCCTCCTGCCCCAGCAGCCCCTTAGAGGTCTCCACTGGGCCTGCAGACC A G RF00017-4575,RF00017-1304 RNACentral:URS0000918622,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143984784..143984884 32194978 MeRIP-seq:(Medium) rs1458306913 Functional Loss SNV dbSNP153 33..33 33 - - - 64834 RMVar_ID_64834 Human_SNP_ID_386139030 m1A Human chr8 + 143985061 143985061 143985061 CAGAGCCTGTTGTCATAATCCCTCTACCCTGCACCATGGGACCTGTCCTCAGAGAGGCCCCTGAC CAGAGCCTGTTGTCATAATCCCTCTACCCTGCCCCATGGGACCTGTCCTCAGAGAGGCCCCTGAC A C RF00017-4575,RF00017-1304 RNACentral:URS0000918622,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143985051..143985181 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 64835 RMVar_ID_64835 Human_SNP_ID_386139502 m1A Human chr8 - 143986138 143986138 143986138 GCCCGACGAGCTGCTCACTCTCTACTTTGAAAACCGCCGACGCTCTGGAGGGGGACCTGTGTTGA GCCCGACGAGCTGCTCACTCTCTACTTTGAAACCCGCCGACGCTCTGGAGGGGGACCTGTGTTGA T G PARP10 Ensembl:ENSG00000178685 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143986098..143986250 26863196 MeRIP-seq:(Medium) rs782672040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1022018,Human_Splice_Rec_1022019,Human_Splice_Rec_1022038,Human_Splice_Rec_1022039,Human_Splice_Rec_1022057,Human_Splice_Rec_1022076,Human_Splice_Rec_1022077,Human_Splice_Rec_1022100,Human_Splice_Rec_1022101,Human_Splice_Rec_1022111,Human_Splice_Rec_1022116,Human_Splice_Rec_1022117,Human_Splice_Rec_1022124,Human_Splice_Rec_1022125,Human_Splice_Rec_1022132,Human_Splice_Rec_1022133,Human_Splice_Rec_1022138,Human_Splice_Rec_1022139,Human_Splice_Rec_1022144,Human_Splice_Rec_1022145,Human_Splice_Rec_1022150,Human_Splice_Rec_1022151,Human_Splice_Rec_1022156,Human_Splice_Rec_1022157,Human_Splice_Rec_1022162,Human_Splice_Rec_1022163,Human_Splice_Rec_1022166,Human_Splice_Rec_1022170,Human_Splice_Rec_1022171,Human_Splice_Rec_1022176,Human_Splice_Rec_1022177,Human_Splice_Rec_1022182,Human_Splice_Rec_1022183 RMVar_hsa_circ_2340 64836 RMVar_ID_64836 Human_SNP_ID_386139536 m1A Human chr8 + 143986204 143986204 143986204 CGGCAGGGGGCAGTCCACGGACCTCCACTGCCACCCCTGCCTCTGCCTCCGCCATTGCAACCCTG CGGCAGGGGGCAGTCCACGGACCTCCACTGCCCCCCCTGCCTCTGCCTCCGCCATTGCAACCCTG A C RF00017-4575,RF00017-1304 RNACentral:URS0000918622,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143986051..143986250 26863196 MeRIP-seq:(Medium) rs782740279 Functional Loss SNV dbSNP153 33..33 33 - - - 64837 RMVar_ID_64837 Human_SNP_ID_386139591 m1A Human chr8 + 143986305 143986305 143986305 CCACCCCTCCTGCCCCTCCCCAGGCCCCTCCAAGGTGTGTCCTCAATGCTCCCCCATTATGGGTG CCACCCCTCCTGCCCCTCCCCAGGCCCCTCCACGGTGTGTCCTCAATGCTCCCCCATTATGGGTG A C RF00017-4575,RF00017-1304 RNACentral:URS0000918622,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143986302..143986425 26863196 MeRIP-seq:(Medium) rs782533879 Functional Loss SNV dbSNP153 33..33 33 - - - 64838 RMVar_ID_64838 Human_SNP_ID_386140699 m1A Human chr8 + 143990175 143990175 143990175 CACCGCGCGGCCGCGCAGCGGACACCGTGCGTACCGGCCTGCGGCGCCCGGCCACCGGTGAGTCC CACCGCGCGGCCGCGCAGCGGACACCGTGCGTGCCGGCCTGCGGCGCCCGGCCACCGGTGAGTCC A G GRINA Ensembl:ENSG00000178719 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:143990076..143990275 26863410 MeRIP-seq:(Medium) rs1195558600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995263,Human_RBP_ID_5514548,Human_RBP_ID_8944498,Human_RBP_ID_9312438,Human_RBP_ID_18426771,Human_RBP_ID_19022278 Human_Splice_Rec_1022189 64839 RMVar_ID_64839 Human_SNP_ID_386141051 m1A Human chr8 - 143991268 143991268 143991268 TGGGGCCCCCCCGGATATCCAGGGTTGGGGGGAGGATAGTTGTCCCCAGACACCAAAAAACTCTT TGGGGCCCCCCCGGATATCCAGGGTTGGGGGGCGGATAGTTGTCCCCAGACACCAAAAAACTCTT T G PARP10 Ensembl:ENSG00000178685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143991174..143991375 26863196 MeRIP-seq:(Medium) rs1388117610 Functional Loss SNV dbSNP153 33..33 33 - - - 64840 RMVar_ID_64840 Human_SNP_ID_386141581 m1A Human chr8 + 143992350 143992350 143992350 TGGCCGTGGGCATCACCACAGCCGTCTGCTTCACCGTCGTCATCTTCTCCATGCAGGTGAGGGGC TGGCCGTGGGCATCACCACAGCCGTCTGCTTCGCCGTCGTCATCTTCTCCATGCAGGTGAGGGGC A G GRINA Ensembl:ENSG00000178719 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143992301..143992379 26863196 MeRIP-seq:(Medium) rs939861519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5225195,Human_RBP_ID_8682983,Human_RBP_ID_17434070,Human_RBP_ID_21564992,Human_RBP_ID_22775772,Human_RBP_ID_27536763 Human_Splice_Rec_1022197,Human_Splice_Rec_1022209,Human_Splice_Rec_1022229,Human_Splice_Rec_1022235,Human_Splice_Rec_1022241,Human_Splice_Rec_1022249,Human_Splice_Rec_1022253 RMVar_hsa_circ_91055,RMVar_hsa_circ_119657,RMVar_hsa_circ_255000,RMVar_hsa_circ_115447,RMVar_hsa_circ_99170,RMVar_hsa_circ_255002,RMVar_hsa_circ_110572,RMVar_hsa_circ_255004,RMVar_hsa_circ_96301,RMVar_hsa_circ_255005,RMVar_hsa_circ_113440,RMVar_hsa_circ_255006,RMVar_hsa_circ_255008,RMVar_hsa_circ_1200,RMVar_hsa_circ_255007 64841 RMVar_ID_64841 Human_SNP_ID_386141933 m1A Human chr8 + 143993257 143993256 143993257 GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCCACCCCCCTGGAGTGCTGCCCTCTGGGGACATGC GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCC_CCCCCCTGGAGTGCTGCCCTCTGGGGACATGC CA C GRINA Ensembl:ENSG00000178719 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1554750901 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_695726,Human_RBP_ID_9222092,Human_RBP_ID_21994953,Human_RBP_ID_24249963 Human_miRNA_ID_659008,Human_miRNA_ID_1421662,Human_miRNA_ID_1706095 RMVar_hsa_circ_91055,RMVar_hsa_circ_255000,RMVar_hsa_circ_115447,RMVar_hsa_circ_99170,RMVar_hsa_circ_255002,RMVar_hsa_circ_110572,RMVar_hsa_circ_96301,RMVar_hsa_circ_255005,RMVar_hsa_circ_255006,RMVar_hsa_circ_121638,RMVar_hsa_circ_107072,RMVar_hsa_circ_255008,RMVar_hsa_circ_255009,RMVar_hsa_circ_255010 64842 RMVar_ID_64842 Human_SNP_ID_386141936 m1A Human chr8 + 143993257 143993257 143993257 GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCCACCCCCCTGGAGTGCTGCCCTCTGGGGACATGC GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCCCCCCCCCTGGAGTGCTGCCCTCTGGGGACATGC A C GRINA Ensembl:ENSG00000178719 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1178802028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695726,Human_RBP_ID_9222092,Human_RBP_ID_21994953,Human_RBP_ID_24249963 Human_miRNA_ID_659008,Human_miRNA_ID_1421662,Human_miRNA_ID_1706095 RMVar_hsa_circ_91055,RMVar_hsa_circ_255000,RMVar_hsa_circ_115447,RMVar_hsa_circ_99170,RMVar_hsa_circ_255002,RMVar_hsa_circ_110572,RMVar_hsa_circ_96301,RMVar_hsa_circ_255005,RMVar_hsa_circ_255006,RMVar_hsa_circ_121638,RMVar_hsa_circ_107072,RMVar_hsa_circ_255008,RMVar_hsa_circ_255009,RMVar_hsa_circ_255010 64843 RMVar_ID_64843 Human_SNP_ID_386141937 m1A Human chr8 + 143993257 143993257 143993257 GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCCACCCCCCTGGAGTGCTGCCCTCTGGGGACATGC GCCTGGCGTAGAGCACCCCTCCCCTCCCCCCCGCCCCCCTGGAGTGCTGCCCTCTGGGGACATGC A G GRINA Ensembl:ENSG00000178719 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1178802028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695726,Human_RBP_ID_9222092,Human_RBP_ID_21994953,Human_RBP_ID_24249963 Human_miRNA_ID_659008,Human_miRNA_ID_1421662,Human_miRNA_ID_1706095 RMVar_hsa_circ_91055,RMVar_hsa_circ_255000,RMVar_hsa_circ_115447,RMVar_hsa_circ_99170,RMVar_hsa_circ_255002,RMVar_hsa_circ_110572,RMVar_hsa_circ_96301,RMVar_hsa_circ_255005,RMVar_hsa_circ_255006,RMVar_hsa_circ_121638,RMVar_hsa_circ_107072,RMVar_hsa_circ_255008,RMVar_hsa_circ_255009,RMVar_hsa_circ_255010 64844 RMVar_ID_64844 Human_SNP_ID_386148360 m1A Human chr8 - 144020470 144020470 144020470 GAGGGGTTCCTCAGAGAAGAGAGTCCTGAGGGAAGAGTGTCCTGCGGGAAGGTGGTCCTGAGAGA GAGGGGTTCCTCAGAGAAGAGAGTCCTGAGGGGAGAGTGTCCTGCGGGAAGGTGGTCCTGAGAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144020460..144020646 26863196 MeRIP-seq:(Medium) rs1415267309 Functional Loss SNV dbSNP153 33..33 33 - - - 64845 RMVar_ID_64845 Human_SNP_ID_386153629 m1A Human chr8 - 144040824 144040822 144040825 GAGGGTGTGTAGCTGGTGGCAACCTGGGGGGCAAGGGCGGGGGCAGAGGCAAGGACGGTGACCGT GAGGGTGTGTAGCTGGTGGCAACCTGGGGGG___GGGCGGGGGCAGAGGCAAGGACGGTGACCGT CTTG C lnc-OPLAH-2 RNACentral:URS00008BF486 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144040819..144040993 26863196 MeRIP-seq:(Medium) rs1554755811 Functional Loss DEL dbSNP153 32..34 33 - - - 64846 RMVar_ID_64846 Human_SNP_ID_386159397 m1A Human chr8 + 144056467 144056467 144056467 GAAGACCACTGCGGCCGGTGCCCCGCACTCGCACATCGTCCACGACCACCGGCCGCTCAGGTATG GAAGACCACTGCGGCCGGTGCCCCGCACTCGCGCATCGTCCACGACCACCGGCCGCTCAGGTATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144056409..144056521 26863196 MeRIP-seq:(Medium) rs782701903 Functional Loss SNV dbSNP153 33..33 33 - - - 64847 RMVar_ID_64847 Human_SNP_ID_386159908 m1A Human chr8 + 144057534 144057532 144057534 CCCCATGGCCACCTCCTCCAGGCTCAGCGGGGAGGCCGGGCAGGGCCCGTTGGTCAGGAAGCTGT CCCCATGGCCACCTCCTCCAGGCTCAGCGGG__GGCCGGGCAGGGCCCGTTGGTCAGGAAGCTGT GGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144057527..144057728 26863196 MeRIP-seq:(Medium) rs782628949 Functional Loss DEL dbSNP153 32..33 33 - - - 64848 RMVar_ID_64848 Human_SNP_ID_386159931 m1A Human chr8 - 144057567 144057567 144057567 GCAAAGCCCTGGAGGCTGTGGCCACTGAGGTCAACAGCTTCCTGACCAACGGGCCCTGCCCGGCC GCAAAGCCCTGGAGGCTGTGGCCACTGAGGTCCACAGCTTCCTGACCAACGGGCCCTGCCCGGCC T G OPLAH Ensembl:ENSG00000178814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144057536..144057857 26863196 MeRIP-seq:(Medium) rs1554759632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094166 RMVar_hsa_circ_114999,RMVar_hsa_circ_255012 64849 RMVar_ID_64849 Human_SNP_ID_386160604 m1A Human chr8 - 144058891 144058891 144058891 ACGGGGCCTCCTGGGCTTTTCTGGAAGGCCGCACGGGGGACCTGCTGGAAGTGCAGCAGCCTGTG ACGGGGCCTCCTGGGCTTTTCTGGAAGGCCGCGCGGGGGACCTGCTGGAAGTGCAGCAGCCTGTG T C OPLAH Ensembl:ENSG00000178814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144058887..144059077 26863196 MeRIP-seq:(Medium) rs1394462037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959543,Human_RBP_ID_5406149,Human_RBP_ID_5534435,Human_RBP_ID_17172440,Human_RBP_ID_19023260 Human_Splice_Rec_1022298,Human_Splice_Rec_1022356 RMVar_hsa_circ_101508,RMVar_hsa_circ_255013 64850 RMVar_ID_64850 Human_SNP_ID_386160659 m1A Human chr8 + 144059018 144059018 144059018 CAGGCGTCCCGGTGCCCGCCTCTCCACGGTGCAGCACCACGCGTTCGTCCACCTCCAGCACCTCT CAGGCGTCCCGGTGCCCGCCTCTCCACGGTGCGGCACCACGCGTTCGTCCACCTCCAGCACCTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144058980..144059063 26863196 MeRIP-seq:(Medium) rs1554760257 Functional Loss SNV dbSNP153 33..33 33 - - - 64851 RMVar_ID_64851 Human_SNP_ID_386166232 m1A Human chr8 - 144078850 144078850 144078850 CCACAGCCAGTGCCTTGGTGTTGCCCTGCTCAATGTAGGCCGAGCCGTCAGCCTGCGCGAACACG CCACAGCCAGTGCCTTGGTGTTGCCCTGCTCATTGTAGGCCGAGCCGTCAGCCTGCGCGAACACG T A AC109322.1 Ensembl:ENSG00000255224 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144078750..144078850 26863410 MeRIP-seq:(Medium) rs1554763100 Functional Loss SNV dbSNP153 33..33 33 - - - 64852 RMVar_ID_64852 Human_SNP_ID_386166573 m1A Human chr8 - 144079902 144079902 144079902 GGACAGACACATGAGCCAGGCCCACTCCTTCCAGCTCACACTCCACTGTCCTCTGTGGGTCTGCC GGACAGACACATGAGCCAGGCCCACTCCTTCCGGCTCACACTCCACTGTCCTCTGTGGGTCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144079900..144080027 26863196 MeRIP-seq:(Medium) rs1470638168 Functional Loss SNV dbSNP153 33..33 33 - - - 64853 RMVar_ID_64853 Human_SNP_ID_386166855 m1A Human chr8 - 144080583 144080579 144080583 GGGTGGCTGGGTGGTCAGTCCCCCAGCAAGATAGAGGCCTCACGCACATGCTGCCGGACCACTCG GGGTGGCTGGGTGGTCAGTCCCCCAGCAAGAT____GCCTCACGCACATGCTGCCGGACCACTCG CCTCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144079972..144080599 32194978 MeRIP-seq:(Medium) rs782787594 Functional Loss DEL dbSNP153 33..36 33 - - - 64854 RMVar_ID_64854 Human_SNP_ID_386167815 m1A Human chr8 + 144083499 144083499 144083499 ACTGCCCTTCCCAGATGAGACCCACGAGCGCTATGTACTGGGGGAGTGGGGTGTGCCTGGGCCCA ACTGCCCTTCCCAGATGAGACCCACGAGCGCTGTGTACTGGGGGAGTGGGGTGTGCCTGGGCCCA A G GPAA1 Ensembl:ENSG00000197858 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144083134..144083531 32194978 MeRIP-seq:(Medium) rs1357847135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19140532 Human_Splice_Rec_1022377,Human_Splice_Rec_1022413,Human_Splice_Rec_1022431,Human_Splice_Rec_1022451,Human_Splice_Rec_1022461,Human_Splice_Rec_1022471,Human_Splice_Rec_1022475 RMVar_hsa_circ_110037,RMVar_hsa_circ_255017 64855 RMVar_ID_64855 Human_SNP_ID_386167935 m1A Human chr8 + 144083768 144083768 144083768 ACGGCATCCTGCGGGCCCCGCGTGCTGCCAGCACCGAGTCGCTTGTGCTCACCGTGCCCTGTGGC ACGGCATCCTGCGGGCCCCGCGTGCTGCCAGCTCCGAGTCGCTTGTGCTCACCGTGCCCTGTGGC A T GPAA1 Ensembl:ENSG00000197858 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144083701..144083875 32194978 MeRIP-seq:(Medium) rs1554763891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4974637,Human_RBP_ID_19023265,Human_RBP_ID_22775774,Human_RBP_ID_24563520 Human_Splice_Rec_1022368,Human_Splice_Rec_1022369,Human_Splice_Rec_1022378,Human_Splice_Rec_1022383,Human_Splice_Rec_1022395,Human_Splice_Rec_1022402,Human_Splice_Rec_1022403,Human_Splice_Rec_1022414,Human_Splice_Rec_1022415,Human_Splice_Rec_1022432,Human_Splice_Rec_1022433,Human_Splice_Rec_1022452,Human_Splice_Rec_1022453,Human_Splice_Rec_1022462,Human_Splice_Rec_1022463,Human_Splice_Rec_1022472,Human_Splice_Rec_1022476,Human_Splice_Rec_1022477,Human_Splice_Rec_1022485 RMVar_hsa_circ_110037,RMVar_hsa_circ_26108,RMVar_hsa_circ_119303,RMVar_hsa_circ_255017,RMVar_hsa_circ_255018 64856 RMVar_ID_64856 Human_SNP_ID_386168042 m1A Human chr8 - 144084027 144084024 144084027 GCAGGACAAGAGAACCTACCAGTGACATTGACATCGTGGTAGGCTTCAAGCCAAGCCTCAGTGCC GCAGGACAAGAGAACCTACCAGTGACATTGAC___GTGGTAGGCTTCAAGCCAAGCCTCAGTGCC CGAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144083976..144084050 26863196 MeRIP-seq:(Medium) rs1228806024 Functional Loss DEL dbSNP153 33..35 33 - - - 64857 RMVar_ID_64857 Human_SNP_ID_386168046 m1A Human chr8 - 144084027 144084027 144084027 GCAGGACAAGAGAACCTACCAGTGACATTGACATCGTGGTAGGCTTCAAGCCAAGCCTCAGTGCC GCAGGACAAGAGAACCTACCAGTGACATTGACGTCGTGGTAGGCTTCAAGCCAAGCCTCAGTGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144083976..144084050 26863196 MeRIP-seq:(Medium) rs782528753 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 64858 RMVar_ID_64858 Human_SNP_ID_386168052 m1A Human chr8 - 144084039 144084039 144084039 GGACCAGGGCAGGCAGGACAAGAGAACCTACCAGTGACATTGACATCGTGGTAGGCTTCAAGCCA GGACCAGGGCAGGCAGGACAAGAGAACCTACCGGTGACATTGACATCGTGGTAGGCTTCAAGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr8:144084001..144084086;chr8:144084001..144084050;chr8:144084003..144084929 26863196,32194978 MeRIP-seq:(Medium) rs782598296 Functional Loss SNV dbSNP153 33..33 33 - - - 64859 RMVar_ID_64859 Human_SNP_ID_386168761 m1A Human chr8 - 144085676 144085676 144085676 CACCATGGTGGTGGCCAGCAGGAAGCCCAGTGAGAAGTTGGTGAGGGCGATGCAGCCCAGCTGCA CACCATGGTGGTGGCCAGCAGGAAGCCCAGTGCGAAGTTGGTGAGGGCGATGCAGCCCAGCTGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144085625..144085744 26863196 MeRIP-seq:(Medium) rs782406808 Functional Loss SNV dbSNP153 33..33 33 - - - 64860 RMVar_ID_64860 Human_SNP_ID_386172391 m1A Human chr8 + 144096448 144096446 144096449 CATACCCCAACAGTGAGGCTGCTCGAGCTGCCAACAACGGAGCATTGCCCCCTGACCTCAGCTAC CATACCCCAACAGTGAGGCTGCTCGAGCTGC___CAACGGAGCATTGCCCCCTGACCTCAGCTAC CCAA C CYC1 Ensembl:ENSG00000179091 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:144096176..144096573 26863196 MeRIP-seq:(Medium) rs1317735832 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_695780,Human_RBP_ID_1694094,Human_RBP_ID_3974256,Human_RBP_ID_4974710,Human_RBP_ID_8683016 Human_Splice_Rec_1022517,Human_Splice_Rec_1022529 RMVar_hsa_circ_5289,RMVar_hsa_circ_107093,RMVar_hsa_circ_90969,RMVar_hsa_circ_255022,RMVar_hsa_circ_110052,RMVar_hsa_circ_255023,RMVar_hsa_circ_372537,RMVar_hsa_circ_255024,RMVar_hsa_circ_116008,RMVar_hsa_circ_92432,RMVar_hsa_circ_255025,RMVar_hsa_circ_255026,RMVar_hsa_circ_255027 64861 RMVar_ID_64861 Human_SNP_ID_386172391 m1A Human chr8 + 144096449 144096446 144096449 ATACCCCAACAGTGAGGCTGCTCGAGCTGCCAACAACGGAGCATTGCCCCCTGACCTCAGCTACA ATACCCCAACAGTGAGGCTGCTCGAGCTGC___CAACGGAGCATTGCCCCCTGACCTCAGCTACA CCAA C CYC1 Ensembl:ENSG00000179091 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144096323..144096490 26863196 MeRIP-seq:(Medium) rs1317735832 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_695781,Human_RBP_ID_1694094,Human_RBP_ID_4974711,Human_RBP_ID_8683016,Human_RBP_ID_27122359 Human_Splice_Rec_1022517,Human_Splice_Rec_1022529 RMVar_hsa_circ_5289,RMVar_hsa_circ_107093,RMVar_hsa_circ_90969,RMVar_hsa_circ_255022,RMVar_hsa_circ_110052,RMVar_hsa_circ_255023,RMVar_hsa_circ_372537,RMVar_hsa_circ_255024,RMVar_hsa_circ_116008,RMVar_hsa_circ_92432,RMVar_hsa_circ_255025,RMVar_hsa_circ_255026,RMVar_hsa_circ_255027 64862 RMVar_ID_64862 Human_SNP_ID_386172506 m1A Human chr8 + 144096667 144096667 144096667 ACCCACCGGGGTGTCACTGCGGGAAGGTCTCTACTTCAACCCCTACTTTCCTGGCCAGGCCATTG ACCCACCGGGGTGTCACTGCGGGAAGGTCTCTCCTTCAACCCCTACTTTCCTGGCCAGGCCATTG A C CYC1 Ensembl:ENSG00000179091 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144096586..144096669 26863196 MeRIP-seq:(Medium) rs749217009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255079,Human_RBP_ID_695785,Human_RBP_ID_1054684,Human_RBP_ID_5480819,Human_RBP_ID_17317255,Human_RBP_ID_17431994,Human_RBP_ID_17714295,Human_RBP_ID_18114094,Human_RBP_ID_22516732,Human_RBP_ID_22836575,Human_RBP_ID_24519714,Human_RBP_ID_27122361,Human_RBP_ID_27363959,Human_RBP_ID_27536809 Human_Splice_Rec_1022518,Human_Splice_Rec_1022519,Human_Splice_Rec_1022530,Human_Splice_Rec_1022531,Human_Splice_Rec_1022539 RMVar_hsa_circ_5289,RMVar_hsa_circ_107093,RMVar_hsa_circ_90969,RMVar_hsa_circ_255022,RMVar_hsa_circ_110052,RMVar_hsa_circ_255023,RMVar_hsa_circ_372537,RMVar_hsa_circ_255024,RMVar_hsa_circ_116008,RMVar_hsa_circ_92432,RMVar_hsa_circ_255025,RMVar_hsa_circ_255026,RMVar_hsa_circ_125966,RMVar_hsa_circ_255027,RMVar_hsa_circ_255028 64863 RMVar_ID_64863 Human_SNP_ID_386172871 m1A Human chr8 + 144097398 144097398 144097398 CAGAACAGGCCCTCAAGCCCAAGAGCCATCCCAGGCCTGTTCAGGCCTCAGCTAAGCCTCTCTTC CAGAACAGGCCCTCAAGCCCAAGAGCCATCCCGGGCCTGTTCAGGCCTCAGCTAAGCCTCTCTTC A G CYC1 Ensembl:ENSG00000179091 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144097351..144097400 32194978 MeRIP-seq:(Medium) rs968347829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695797,Human_RBP_ID_9222102,Human_RBP_ID_17666041,Human_RBP_ID_18172912,Human_RBP_ID_18196645,Human_RBP_ID_18893489,Human_RBP_ID_26833073 RMVar_hsa_circ_81062,RMVar_hsa_circ_107093,RMVar_hsa_circ_90969,RMVar_hsa_circ_255022,RMVar_hsa_circ_110052,RMVar_hsa_circ_255023,RMVar_hsa_circ_255024,RMVar_hsa_circ_116008,RMVar_hsa_circ_92432,RMVar_hsa_circ_255026,RMVar_hsa_circ_255027,RMVar_hsa_circ_255030,RMVar_hsa_circ_255031,RMVar_hsa_circ_98085 64864 RMVar_ID_64864 Human_SNP_ID_386173333 m1A Human chr8 - 144098991 144098991 144098991 GGAAGCAACAACTGTCTCTCTTCCCCCAGCCCAGCTGGTCCTGTCCTTCCTGCACCTTCATCAAT GGAAGCAACAACTGTCTCTCTTCCCCCAGCCCGGCTGGTCCTGTCCTTCCTGCACCTTCATCAAT T C SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144098884..144099038 26863196 MeRIP-seq:(Medium) rs762338240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957957,Human_RBP_ID_19141993,Human_RBP_ID_22689487 Human_Splice_Rec_1022544,Human_Splice_Rec_1022558,Human_Splice_Rec_1022572 RMVar_hsa_circ_88544,RMVar_hsa_circ_50110,RMVar_hsa_circ_255033 64865 RMVar_ID_64865 Human_SNP_ID_386173493 m1A Human chr8 - 144099327 144099327 144099327 GCGCAGCCTTGCCTCTTACGGGGTTCGGCAGGATGGGGACCCTGCTTTCCTCTACTTGCTGTCAG GCGCAGCCTTGCCTCTTACGGGGTTCGGCAGGTTGGGGACCCTGCTTTCCTCTACTTGCTGTCAG T A SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144098930..144100796 32194978 MeRIP-seq:(Medium) rs1378764618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18452320 Human_Splice_Rec_1022541,Human_Splice_Rec_1022555,Human_Splice_Rec_1022571 RMVar_hsa_circ_17966,RMVar_hsa_circ_88544,RMVar_hsa_circ_50110,RMVar_hsa_circ_255033,RMVar_hsa_circ_106967,RMVar_hsa_circ_255034 64866 RMVar_ID_64866 Human_SNP_ID_386173494 m1A Human chr8 - 144099327 144099327 144099327 GCGCAGCCTTGCCTCTTACGGGGTTCGGCAGGATGGGGACCCTGCTTTCCTCTACTTGCTGTCAG GCGCAGCCTTGCCTCTTACGGGGTTCGGCAGGGTGGGGACCCTGCTTTCCTCTACTTGCTGTCAG T C SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144098930..144100796 32194978 MeRIP-seq:(Medium) rs1378764618 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18452320 Human_Splice_Rec_1022541,Human_Splice_Rec_1022555,Human_Splice_Rec_1022571 RMVar_hsa_circ_17966,RMVar_hsa_circ_88544,RMVar_hsa_circ_50110,RMVar_hsa_circ_255033,RMVar_hsa_circ_106967,RMVar_hsa_circ_255034 64867 RMVar_ID_64867 Human_SNP_ID_386173863 m1A Human chr8 + 144100023 144100022 144100024 GTGGAGGCTTCCGGGGGACTGGGCAGGGAGACAGGGCATGCTTCTGGGCCCAAGGCTGGTGGTGA GTGGAGGCTTCCGGGGGACTGGGCAGGGAGAC__GGCATGCTTCTGGGCCCAAGGCTGGTGGTGA CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144099976..144100099 26863196 MeRIP-seq:(Medium) rs764352218 Functional Loss DEL dbSNP153 33..34 33 - - - 64868 RMVar_ID_64868 Human_SNP_ID_386173868 m1A Human chr8 - 144100032 144100032 144100032 AAGAGCAACTCACCACCAGCCTTGGGCCCAGAAGCATGCCCTGTCTCCCTGCCCAGTCCCCCGGA AAGAGCAACTCACCACCAGCCTTGGGCCCAGACGCATGCCCTGTCTCCCTGCCCAGTCCCCCGGA T G SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144099981..144102746 26863196 MeRIP-seq:(Medium) rs763145216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19023297,Human_RBP_ID_26359534,Human_RBP_ID_26832503 Human_Splice_Rec_1022548,Human_Splice_Rec_1022564,Human_Splice_Rec_1022576,Human_Splice_Rec_1022586,Human_Splice_Rec_1022600 RMVar_hsa_circ_88544,RMVar_hsa_circ_50110,RMVar_hsa_circ_255033 64869 RMVar_ID_64869 Human_SNP_ID_386174702 m1A Human chr8 + 144102565 144102564 144102565 AAAGTGCTGGAATTACAGGCGTGAGCCACCCCACCCGGCCACTAATTCCATCTTCTAAGCATCTC AAAGTGCTGGAATTACAGGCGTGAGCCACCCC_CCCGGCCACTAATTCCATCTTCTAAGCATCTC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144102561..144102735 26863196 MeRIP-seq:(Medium) rs1459866112 Functional Loss DEL dbSNP153 33..33 33 - - - 64870 RMVar_ID_64870 Human_SNP_ID_386174848 m1A Human chr8 + 144103018 144103018 144103018 CCCAACCAGGACTGGGGGGCCAAGGCTATTCCAAATTGTAATTGTATCCATTACAGGGCACTGAC CCCAACCAGGACTGGGGGGCCAAGGCTATTCCGAATTGTAATTGTATCCATTACAGGGCACTGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144103016..144103153 26863196 MeRIP-seq:(Medium) rs761863965 Functional Loss SNV dbSNP153 33..33 33 - - - 64871 RMVar_ID_64871 Human_SNP_ID_386175190 m1A Human chr8 - 144103649 144103649 144103649 CACGCCGCGGTGAGGCCGCTGGGCGCCGGGCCAGACGCCGAGGCACAGCTGCGGAGGCTGCAGCT CACGCCGCGGTGAGGCCGCTGGGCGCCGGGCCGGACGCCGAGGCACAGCTGCGGAGGCTGCAGCT T C SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144103602..144103775;chr8:144103601..144103725 26863196 MeRIP-seq:(Medium) rs1408686382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796082,Human_RBP_ID_4995801,Human_RBP_ID_22115780,Human_RBP_ID_23216218 Human_Splice_Rec_1022545,Human_Splice_Rec_1022561,Human_Splice_Rec_1022607 RMVar_hsa_circ_88544,RMVar_hsa_circ_255033,RMVar_hsa_circ_88115,RMVar_hsa_circ_255036 64872 RMVar_ID_64872 Human_SNP_ID_386175243 m1A Human chr8 - 144103742 144103742 144103742 TGGGACCCGGCCGGACCGGAGATGGCGCCGCCAGCGGGCGGGGCGGCGGCGGCGGCCTCGGACTT TGGGACCCGGCCGGACCGGAGATGGCGCCGCCCGCGGGCGGGGCGGCGGCGGCGGCCTCGGACTT T G SHARPIN Ensembl:ENSG00000179526 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144103568..144103749 26863196 MeRIP-seq:(Medium) rs1324923547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995285,Human_RBP_ID_26795162 RMVar_hsa_circ_88544,RMVar_hsa_circ_255033,RMVar_hsa_circ_88115,RMVar_hsa_circ_255036 64873 RMVar_ID_64873 Human_SNP_ID_386175723 m1A Human chr8 + 144104809 144104808 144104809 GCCTGCGCACCGGCACCGACGCGGAGCGACCCAGCCCAGCCAGACCCGGCCCGGCGCGGCCTGAT GCCTGCGCACCGGCACCGACGCGGAGCGACCC_GCCCAGCCAGACCCGGCCCGGCGCGGCCTGAT CA C MAF1 Ensembl:ENSG00000179632 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144104516..144104875;chr8:144104407..144104885;chr8:144104439..144104894;chr8:144104451..144104880 26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1564316996 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22534445,Human_RBP_ID_26554048 Human_Splice_Rec_1022613,Human_Splice_Rec_1022627 RMVar_hsa_circ_115766,RMVar_hsa_circ_118118,RMVar_hsa_circ_255037,RMVar_hsa_circ_255038 64874 RMVar_ID_64874 Human_SNP_ID_386175724 m1A Human chr8 + 144104809 144104809 144104809 GCCTGCGCACCGGCACCGACGCGGAGCGACCCAGCCCAGCCAGACCCGGCCCGGCGCGGCCTGAT GCCTGCGCACCGGCACCGACGCGGAGCGACCCGGCCCAGCCAGACCCGGCCCGGCGCGGCCTGAT A G MAF1 Ensembl:ENSG00000179632 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144104516..144104875;chr8:144104407..144104885;chr8:144104439..144104894;chr8:144104451..144104880 26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs971937396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22534445,Human_RBP_ID_26554048 Human_Splice_Rec_1022613,Human_Splice_Rec_1022627 RMVar_hsa_circ_115766,RMVar_hsa_circ_118118,RMVar_hsa_circ_255037,RMVar_hsa_circ_255038 64875 RMVar_ID_64875 Human_SNP_ID_386176027 m1A Human chr8 + 144105608 144105608 144105608 AGGGCTGAAGGCAGGGCCCCAAGGGGCCAGATAGATACCCATGGTCTGGTCTCTCACTCCCCAGG AGGGCTGAAGGCAGGGCCCCAAGGGGCCAGATGGATACCCATGGTCTGGTCTCTCACTCCCCAGG A G MAF1 Ensembl:ENSG00000179632 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144105606..144105740 26863196 MeRIP-seq:(Medium) rs947656490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26795773 RMVar_hsa_circ_115766,RMVar_hsa_circ_118118,RMVar_hsa_circ_255037,RMVar_hsa_circ_255038 64876 RMVar_ID_64876 Human_SNP_ID_386176556 m1A Human chr8 + 144106926 144106926 144106926 AGGAGGTGGAGGAAGAAAGCAGAAGCGGGGGCAGTGGGGCCGAGGAGACCAGCACCATGGAGGAG AGGAGGTGGAGGAAGAAAGCAGAAGCGGGGGCCGTGGGGCCGAGGAGACCAGCACCATGGAGGAG A C MAF1 Ensembl:ENSG00000179632 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144106884..144106966 26863196 MeRIP-seq:(Medium) rs373891300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845860,Human_RBP_ID_18196822,Human_RBP_ID_23216219 Human_Splice_Rec_1022624,Human_Splice_Rec_1022625,Human_Splice_Rec_1022636,Human_Splice_Rec_1022637,Human_Splice_Rec_1022650,Human_Splice_Rec_1022651,Human_Splice_Rec_1022666,Human_Splice_Rec_1022668 RMVar_hsa_circ_115766,RMVar_hsa_circ_255038,RMVar_hsa_circ_93211,RMVar_hsa_circ_88454,RMVar_hsa_circ_97054,RMVar_hsa_circ_255039,RMVar_hsa_circ_255040,RMVar_hsa_circ_105353,RMVar_hsa_circ_255042,RMVar_hsa_circ_255043 64877 RMVar_ID_64877 Human_SNP_ID_386176710 m1A Human chr8 + 144107246 144107246 144107246 GCTGCCACAGTCCTGGCACTGCCCAAGGCCATACCTGCCTAGCCCTTTGGCTCCATCCTGTGGAT GCTGCCACAGTCCTGGCACTGCCCAAGGCCATTCCTGCCTAGCCCTTTGGCTCCATCCTGTGGAT A T MAF1 Ensembl:ENSG00000179632 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144107076..144107525 32194978 MeRIP-seq:(Medium) rs1564318569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4974861,Human_RBP_ID_17666220,Human_RBP_ID_18196648,Human_RBP_ID_27363990 RMVar_hsa_circ_115766,RMVar_hsa_circ_255038,RMVar_hsa_circ_93211,RMVar_hsa_circ_88454,RMVar_hsa_circ_97054,RMVar_hsa_circ_255039,RMVar_hsa_circ_255040,RMVar_hsa_circ_105353,RMVar_hsa_circ_255042,RMVar_hsa_circ_109036,RMVar_hsa_circ_255043,RMVar_hsa_circ_255044 64878 RMVar_ID_64878 Human_SNP_ID_386186351 m1A Human chr8 - 144137814 144137806 144137814 GCCTCCCCCATGTCGAGCGACACTCTGCTGCCACCCGACCGGTGCCAGCGGTCCGCTTAGGGGTC GCCTCCCCCATGTCGAGCGACACTCTGCTGCC________GGTGCCAGCGGTCCGCTTAGGGGTC CGGTCGGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144137799..144137951 26863196 MeRIP-seq:(Medium) rs1362994944 Functional Loss DEL dbSNP153 33..40 33 - - - 64879 RMVar_ID_64879 Human_SNP_ID_386186424 m1A Human chr8 + 144138017 144138017 144138017 CTGCGGACCCGGCCGCGCGCTGTTGGCGGGGCAGGCGGCGCTGCTGCAGGCGCTGATGGAGCTGG CTGCGGACCCGGCCGCGCGCTGTTGGCGGGGCGGGCGGCGCTGCTGCAGGCGCTGATGGAGCTGG A G HGH1 Ensembl:ENSG00000235173 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144138009..144138221 26863196 MeRIP-seq:(Medium) rs1249007155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17172446,Human_RBP_ID_26766072 64880 RMVar_ID_64880 Human_SNP_ID_386194114 m1A Human chr8 - 144167454 144167434 144167454 CCGGCCACTCCACCCCAACTGGCCACTCCACCACAACAACCGGCCACTCCACCCAACAACCGGCC CCGGCCACTCCACCCCAACTGGCCACTCCACC____________________CCAACAACCGGCC GGTGGAGTGGCCGGTTGTTGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:144167345..144167568 26863196 MeRIP-seq:(Medium) rs1421289462 Functional Loss DEL dbSNP153 33..52 33 - - - 64881 RMVar_ID_64881 Human_SNP_ID_386194122 m1A Human chr8 - 144167454 144167452 144167455 CCGGCCACTCCACCCCAACTGGCCACTCCACCACAACAACCGGCCACTCCACCCAACAACCGGCC CCGGCCACTCCACCCCAACTGGCCACTCCAC___AACAACCGGCCACTCCACCCAACAACCGGCC TGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:144167345..144167568 26863196 MeRIP-seq:(Medium) rs1459723423 Functional Loss DEL dbSNP153 32..34 33 - - - 64882 RMVar_ID_64882 Human_SNP_ID_386194123 m1A Human chr8 - 144167454 144167453 144167454 CCGGCCACTCCACCCCAACTGGCCACTCCACCACAACAACCGGCCACTCCACCCAACAACCGGCC CCGGCCACTCCACCCCAACTGGCCACTCCACC_CAACAACCGGCCACTCCACCCAACAACCGGCC GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:144167345..144167568 26863196 MeRIP-seq:(Medium) rs1317325766 Functional Loss DEL dbSNP153 33..33 33 - - - 64883 RMVar_ID_64883 Human_SNP_ID_386194124 m1A Human chr8 - 144167454 144167454 144167454 CCGGCCACTCCACCCCAACTGGCCACTCCACCACAACAACCGGCCACTCCACCCAACAACCGGCC CCGGCCACTCCACCCCAACTGGCCACTCCACCCCAACAACCGGCCACTCCACCCAACAACCGGCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:144167345..144167568 26863196 MeRIP-seq:(Medium) rs867625527 Functional Loss SNV dbSNP153 33..33 33 - - - 64884 RMVar_ID_64884 Human_SNP_ID_386199376 m1A Human chr8 + 144185407 144185407 144185407 CAAAACGTTATGTTTTATACCTAGTTCTTTGAAATAAGTGAATTAAATACTTAAGCTGCTGCCTC CAAAACGTTATGTTTTATACCTAGTTCTTTGAGATAAGTGAATTAAATACTTAAGCTGCTGCCTC A G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144185405..144185684 26863196 MeRIP-seq:(Medium) rs576619329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47501,RMVar_hsa_circ_323727,RMVar_hsa_circ_309755,RMVar_hsa_circ_70838,RMVar_hsa_circ_36901,RMVar_hsa_circ_255048,RMVar_hsa_circ_270819,RMVar_hsa_circ_255050,RMVar_hsa_circ_89018,RMVar_hsa_circ_255052 64885 RMVar_ID_64885 Human_SNP_ID_386204139 m1A Human chr8 + 144202334 144202267 144202334 GGAAGGCAGCGACCCGCTCTGTGTGGAGGGGCAGGGAGGGAAGTGTCCCCTCTGTGGAGGGGAAA _________________________________GGGAGGGAAGTGTCCCCTCTGTGGAGGGGAAA GGGGAGGGGAGAGCCCGCTCTCTGTGGAGGGGTTGGGAAGGCAGCGACCCGCTCTGTGTGGAGGGGCA G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144202325..144202488 26863196 MeRIP-seq:(Medium) rs1564463565 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_268021,Human_RBP_ID_3885627,Human_RBP_ID_8221725,Human_RBP_ID_9441561,Human_RBP_ID_18961296,Human_RBP_ID_26795776 RMVar_hsa_circ_9897,RMVar_hsa_circ_47501,RMVar_hsa_circ_70838,RMVar_hsa_circ_89018,RMVar_hsa_circ_255052,RMVar_hsa_circ_112785,RMVar_hsa_circ_119769,RMVar_hsa_circ_76813,RMVar_hsa_circ_47597,RMVar_hsa_circ_255055,RMVar_hsa_circ_255056,RMVar_hsa_circ_255057,RMVar_hsa_circ_111027,RMVar_hsa_circ_127687,RMVar_hsa_circ_269616,RMVar_hsa_circ_255058,RMVar_hsa_circ_91975,RMVar_hsa_circ_255060,RMVar_hsa_circ_255061 64886 RMVar_ID_64886 Human_SNP_ID_386204344 m1A Human chr8 + 144202669 144202669 144202669 CGCAGGCTCTCTGTGGAGAGGCGGGGAGGGGGAGCACCCGCTCTCTGTGGAGGGGTTGGGAGGGG CGCAGGCTCTCTGTGGAGAGGCGGGGAGGGGGGGCACCCGCTCTCTGTGGAGGGGTTGGGAGGGG A G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144202664..144202774 26863196 MeRIP-seq:(Medium) rs1490601339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3886601,Human_RBP_ID_8221729 RMVar_hsa_circ_9897,RMVar_hsa_circ_47501,RMVar_hsa_circ_70838,RMVar_hsa_circ_89018,RMVar_hsa_circ_255052,RMVar_hsa_circ_112785,RMVar_hsa_circ_119769,RMVar_hsa_circ_76813,RMVar_hsa_circ_47597,RMVar_hsa_circ_255055,RMVar_hsa_circ_255056,RMVar_hsa_circ_255057,RMVar_hsa_circ_111027,RMVar_hsa_circ_127687,RMVar_hsa_circ_269616,RMVar_hsa_circ_255058,RMVar_hsa_circ_91975,RMVar_hsa_circ_255060,RMVar_hsa_circ_255061 64887 RMVar_ID_64887 Human_SNP_ID_386210364 m1A Human chr8 + 144222698 144222698 144222698 GTGGGAGCAGGCATAGGTGTGGATGTGGGTGCAGGTAGGTACAGATGCAGGTATGGATGCAGGCA GTGGGAGCAGGCATAGGTGTGGATGTGGGTGCGGGTAGGTACAGATGCAGGTATGGATGCAGGCA A G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144222692..144222839 26863196 MeRIP-seq:(Medium) rs1317634155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9897,RMVar_hsa_circ_47501,RMVar_hsa_circ_70838,RMVar_hsa_circ_112785,RMVar_hsa_circ_76813,RMVar_hsa_circ_47597,RMVar_hsa_circ_255056,RMVar_hsa_circ_255057,RMVar_hsa_circ_127687,RMVar_hsa_circ_269616,RMVar_hsa_circ_91975,RMVar_hsa_circ_255060,RMVar_hsa_circ_255061,RMVar_hsa_circ_337321 64888 RMVar_ID_64888 Human_SNP_ID_386219352 m1A Human chr8 - 144257520 144257520 144257520 AGATCTGGTGATGGGCCCCATGAGGCTTCTGGACGGTTGGGTACACAGGGCTGGTGATGCCGGCA AGATCTGGTGATGGGCCCCATGAGGCTTCTGGGCGGTTGGGTACACAGGGCTGGTGATGCCGGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144257470..144257598 26863196 MeRIP-seq:(Medium) rs1328573504 Functional Loss SNV dbSNP153 33..33 33 - - - 64889 RMVar_ID_64889 Human_SNP_ID_386221239 m1A Human chr8 - 144262995 144262981 144262996 CCGTTCCGCCGCAGCCACGGACAGGTGCAGCGAGTGGCCTTCCACCCTGCCCGGCCCTTCCTGTT CCGTTCCGCCGCAGCCACGGACAGGTGCAGC_______________CTGCCCGGCCCTTCCTGTT GGGTGGAAGGCCACTC G BOP1 Ensembl:ENSG00000261236 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:144262947..144263070;chr8:144262945..144263087 26863196 MeRIP-seq:(Medium) rs1554836670 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_9313717 RMVar_hsa_circ_97175,RMVar_hsa_circ_114726,RMVar_hsa_circ_117736,RMVar_hsa_circ_102549,RMVar_hsa_circ_103634,RMVar_hsa_circ_92347,RMVar_hsa_circ_95174,RMVar_hsa_circ_87325,RMVar_hsa_circ_255067,RMVar_hsa_circ_255071,RMVar_hsa_circ_75767,RMVar_hsa_circ_81696,RMVar_hsa_circ_255073,RMVar_hsa_circ_255072,RMVar_hsa_circ_255069,RMVar_hsa_circ_255070,RMVar_hsa_circ_255068,RMVar_hsa_circ_255065,RMVar_hsa_circ_255066,RMVar_hsa_circ_255064,RMVar_hsa_circ_77139,RMVar_hsa_circ_98981,RMVar_hsa_circ_255077,RMVar_hsa_circ_255078 64890 RMVar_ID_64890 Human_SNP_ID_386221596 m1A Human chr8 + 144264059 144264059 144264059 TCGAAGCGTTCCTGGATGAAGCGTCCGTAGGCAGGCACGGCCCGCAGGCTCGGGAACTTGCGTGG TCGAAGCGTTCCTGGATGAAGCGTCCGTAGGCGGGCACGGCCCGCAGGCTCGGGAACTTGCGTGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:144263941..144264150 26863196 MeRIP-seq:(Medium) rs1276028523 Functional Loss SNV dbSNP153 33..33 33 - - - 64891 RMVar_ID_64891 Human_SNP_ID_386222433 m1A Human chr8 + 144266542 144266533 144266542 GAGACCCCGCGCCTCGCCCCGGCCGGCCCGCGAGGCCCGCGGCGGCCGCAGGAGGCGGCATGAGC GAGACCCCGCGCCTCGCCCCGGCC_________GGCCCGCGGCGGCCGCAGGAGGCGGCATGAGC CGGCCCGCGA C SCX Ensembl:ENSG00000260428 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144266540..144266671 26863196 MeRIP-seq:(Medium) rs1204516697 Functional Loss DEL dbSNP153 25..33 33 - - - 64892 RMVar_ID_64892 Human_SNP_ID_386224078 m1A Human chr8 - 144271439 144271436 144271440 CATTGTAATCGGAGAGGGGCTGGGGAAGAGAGAGACGGAGCGAGGGCGGCTGACCCCACGCTCCC CATTGTAATCGGAGAGGGGCTGGGGAAGAGA____CGGAGCGAGGGCGGCTGACCCCACGCTCCC GTCTC G BOP1 Ensembl:ENSG00000261236 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144271436..144271522 26863196 MeRIP-seq:(Medium) rs1162154354 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3885644,Human_RBP_ID_8221764 64893 RMVar_ID_64893 Human_SNP_ID_386224361 m1A Human chr8 + 144272404 144272404 144272404 TCCCCTGCAGAACAGCCCCGGCCTTGGGACGTACACCCAGACCCAGCTCTCCCCAGCCGGCCTCC TCCCCTGCAGAACAGCCCCGGCCTTGGGACGTGCACCCAGACCCAGCTCTCCCCAGCCGGCCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144272402..144272578 26863196 MeRIP-seq:(Medium) rs1413646904 Functional Loss SNV dbSNP153 33..33 33 - - - 64894 RMVar_ID_64894 Human_SNP_ID_386230486 m1A Human chr8 + 144291327 144291327 144291327 GTTCGGGCTCAGACCGCCGCTTCTCCGGCCGCACGCTCGGCGCCGCCGTGCGCCCCGCACCCCGC GTTCGGGCTCAGACCGCCGCTTCTCCGGCCGCCCGCTCGGCGCCGCCGTGCGCCCCGCACCCCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144289204..144291400 26863410 MeRIP-seq:(Medium) rs782340581 Functional Loss SNV dbSNP153 33..33 33 - - - 64895 RMVar_ID_64895 Human_SNP_ID_386230509 m1A Human chr8 + 144291362 144291362 144291362 CTCGGCGCCGCCGTGCGCCCCGCACCCCGCGAACCCGCCATGCCCCACCGCGCGCCGGCCGCCAC CTCGGCGCCGCCGTGCGCCCCGCACCCCGCGACCCCGCCATGCCCCACCGCGCGCCGGCCGCCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144289053..144291450;chr8:144289066..144291450 26863196 MeRIP-seq:(Medium) rs1554840207 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 64896 RMVar_ID_64896 Human_SNP_ID_386236087 m1A Human chr8 - 144309865 144309865 144309865 CTGCTTCATGGCCAGGAGCTTGGAGTCCATGCACTCCTGCTTCCCCTTCATCAGCTGCACGTCCG CTGCTTCATGGCCAGGAGCTTGGAGTCCATGCGCTCCTGCTTCCCCTTCATCAGCTGCACGTCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144309817..144309913 26863196 MeRIP-seq:(Medium) rs782506952 Functional Loss SNV dbSNP153 33..33 33 - - - 64897 RMVar_ID_64897 Human_SNP_ID_386236535 m1A Human chr8 - 144311251 144311251 144311251 GGGGCCCCCGCCGGCCCTCTGGCCCTGCCCCCACCTTGTTGACGACTTTCTGTTGCTGGGCATGC GGGGCCCCCGCCGGCCCTCTGGCCCTGCCCCCGCCTTGTTGACGACTTTCTGTTGCTGGGCATGC T C lnc-DGAT1-3 RNACentral:URS0000D5DA36 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144311239..144311314 26863196 MeRIP-seq:(Medium) rs1457651230 Functional Loss SNV dbSNP153 33..33 33 - - - 64898 RMVar_ID_64898 Human_SNP_ID_386236793 m1A Human chr8 - 144311795 144311795 144311795 ATGCTCCCGCCGGGGGAGGCCATGGGGCTGGCAGGAGCCAGCTCGGTGATGTCGGAGATGATGGG ATGCTCCCGCCGGGGGAGGCCATGGGGCTGGCGGGAGCCAGCTCGGTGATGTCGGAGATGATGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:144311603..144311850 26863196 MeRIP-seq:(Medium) rs782562311 Functional Loss SNV dbSNP153 33..33 33 - - - 64899 RMVar_ID_64899 Human_SNP_ID_386236980 m1A Human chr8 - 144312122 144312122 144312122 GCGTCCGTGAGGGCTGTGACGGAGGCGGGGGCAGGTTCACTCTCCCGCAGGATGGAGTCAATGAG GCGTCCGTGAGGGCTGTGACGGAGGCGGGGGCGGGTTCACTCTCCCGCAGGATGGAGTCAATGAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr8:144311976..144312179;chr8:144311950..144312159 26863196 MeRIP-seq:(Medium) rs200842781 Functional Loss SNV dbSNP153 33..33 33 - - - 64900 RMVar_ID_64900 Human_SNP_ID_386238396 m1A Human chr8 + 144314340 144314340 144314340 CCAAGGACCCCACTGTCTCCTAGAGGCCCCGGAGGAGCTGGGCCAGCCGCCCACCCCCACCCCCA CCAAGGACCCCACTGTCTCCTAGAGGCCCCGGTGGAGCTGGGCCAGCCGCCCACCCCCACCCCCA A T HSF1 Ensembl:ENSG00000185122 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144314291..144314416 26863196 MeRIP-seq:(Medium) rs782774400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17434082 64901 RMVar_ID_64901 Human_SNP_ID_386238511 m1A Human chr8 - 144314608 144314608 144314608 GAGCGGGGAACGGGACAGTTGTGTAAAAATCCAAAATACAATTCTGACTATGAACAACCTGCAGG GAGCGGGGAACGGGACAGTTGTGTAAAAATCCGAAATACAATTCTGACTATGAACAACCTGCAGG T C DGAT1,AC233992.1 Ensembl:ENSG00000185000,Ensembl:ENSG00000254690 Protein coding,lincRNA 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144313500..144314675 32194978 MeRIP-seq:(Medium) rs1230448756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3886644,Human_RBP_ID_5631073,Human_RBP_ID_21905619 64902 RMVar_ID_64902 Human_SNP_ID_386240286 m1A Human chr8 + 144318564 144318564 144318564 TGCAGCAGCAGTCCCGCCTGCTCCGTCAGGGCACCCTGGAGTGGGGAGCAGAGCACTCAACCAGG TGCAGCAGCAGTCCCGCCTGCTCCGTCAGGGCCCCCTGGAGTGGGGAGCAGAGCACTCAACCAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144318476..144318743 32194978 MeRIP-seq:(Medium) rs1554847677 Functional Loss SNV dbSNP153 33..33 33 - - - 64903 RMVar_ID_64903 Human_SNP_ID_386241603 m1A Human chr8 + 144323025 144323025 144323025 GGGAGCAGGGGCACGAGGCCCAACTGCCCAGCAGCCTCTCTGGGCTGTCTGTCTGGGGGCCTCTC GGGAGCAGGGGCACGAGGCCCAACTGCCCAGCCGCCTCTCTGGGCTGTCTGTCTGGGGGCCTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144323022..144323244 26863196 MeRIP-seq:(Medium) rs1177758025 Functional Loss SNV dbSNP153 33..33 33 - - - 64904 RMVar_ID_64904 Human_SNP_ID_386242578 m1A Human chr8 + 144326588 144326588 144326588 CGCCGCCGCAGGCCCGCCGCCGCCGTGGCTCGAGGGCCGCGACCCTGTCCTCCGGCGCCGGGAGC CGCCGCCGCAGGCCCGCCGCCGCCGTGGCTCGTGGGCCGCGACCCTGTCCTCCGGCGCCGGGAGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144326426..144326850;chr8:144326492..144326626;chr8:144326403..144326900;chr8:144321383..144326875 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1232613286 Functional Loss SNV dbSNP153 33..33 33 - - - 64905 RMVar_ID_64905 Human_SNP_ID_386253787 m1A Human chr8 - 144358727 144358727 144358727 GTCCGGTCCCTGCGCCTCCCGGTCCCGCGCCCAGTGCGCTCCCGCTCCAGTGCCGGCTTCCCGCC GTCCGGTCCCTGCGCCTCCCGGTCCCGCGCCCTGTGCGCTCCCGCTCCAGTGCCGGCTTCCCGCC T A FBXL6 Ensembl:ENSG00000182325 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144358601..144358868 26863196 MeRIP-seq:(Medium) rs369644400 Functional Loss SNV dbSNP153 33..33 33 - - - 64906 RMVar_ID_64906 Human_SNP_ID_386253847 m1A Human chr8 - 144358927 144358927 144358927 GCGGGGCTGGAGTCAACGCCACCACCACCCCAAGCCGGACGCCGGGAAAGGGCGCCTACCAGGAG GCGGGGCTGGAGTCAACGCCACCACCACCCCACGCCGGACGCCGGGAAAGGGCGCCTACCAGGAG T G FBXL6 Ensembl:ENSG00000182325 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144358876..144359050 32194978 MeRIP-seq:(Medium) rs1279895336 Functional Loss SNV dbSNP153 33..33 33 - - - 64907 RMVar_ID_64907 Human_SNP_ID_386253974 m1A Human chr8 + 144359273 144359273 144359273 AAGAACTGGCTGTGACCTTTGCCCTGACCTGGAAGGGCCCAGCCTTGGGCTGAATGGCAGCACCC AAGAACTGGCTGTGACCTTTGCCCTGACCTGGGAGGGCCCAGCCTTGGGCTGAATGGCAGCACCC A G SLC52A2 Ensembl:ENSG00000185803 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144359238..144359315 26863196 MeRIP-seq:(Medium) rs1554853720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695869,Human_RBP_ID_4995306,Human_RBP_ID_22465381 Human_Splice_Rec_1023682,Human_Splice_Rec_1023688,Human_Splice_Rec_1023692,Human_Splice_Rec_1023700,Human_Splice_Rec_1023708,Human_Splice_Rec_1023714,Human_Splice_Rec_1023722,Human_Splice_Rec_1023726,Human_Splice_Rec_1023736,Human_Splice_Rec_1023740,Human_Splice_Rec_1023748,Human_Splice_Rec_1023749,Human_Splice_Rec_1023752 64908 RMVar_ID_64908 Human_SNP_ID_386254706 m1A Human chr8 - 144360703 144360703 144360703 CTTCATGTCCCCCTGTGCTCACCACGAGGACCACCCCCGCCGAGGTGCCCACCAGGGGCGGGCAG CTTCATGTCCCCCTGTGCTCACCACGAGGACCCCCCCCGCCGAGGTGCCCACCAGGGGCGGGCAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144360626..144360725 32194978 MeRIP-seq:(Medium) rs1554854486 Functional Loss SNV dbSNP153 33..33 33 - - - 64909 RMVar_ID_64909 Human_SNP_ID_386254845 m1A Human chr8 - 144360940 144360934 144360940 ACGTGATAGATGCTGGTCGGGGGGAACATAGCAACAGCGCCGAGCAGAGAGCCCACCTGGATGGC ACGTGATAGATGCTGGTCGGGGGGAACATAGC______GCCGAGCAGAGAGCCCACCTGGATGGC CGCTGTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144360801..144361000 32194978 MeRIP-seq:(Medium) rs782354792 Functional Loss DEL dbSNP153 33..38 33 - - - 64910 RMVar_ID_64910 Human_SNP_ID_386254851 m1A Human chr8 + 144360944 144360944 144360944 TCCAGGTGGGCTCTCTGCTCGGCGCTGTTGCTATGTTCCCCCCGACCAGCATCTATCACGTGTTC TCCAGGTGGGCTCTCTGCTCGGCGCTGTTGCTCTGTTCCCCCCGACCAGCATCTATCACGTGTTC A C SLC52A2 Ensembl:ENSG00000185803 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144360893..144361156 26863196 MeRIP-seq:(Medium) rs560659799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695874,Human_RBP_ID_18893579,Human_RBP_ID_22776138,Human_RBP_ID_27536851 Clinvar_Rec_256 64911 RMVar_ID_64911 Human_SNP_ID_386254852 m1A Human chr8 + 144360944 144360944 144360944 TCCAGGTGGGCTCTCTGCTCGGCGCTGTTGCTATGTTCCCCCCGACCAGCATCTATCACGTGTTC TCCAGGTGGGCTCTCTGCTCGGCGCTGTTGCTGTGTTCCCCCCGACCAGCATCTATCACGTGTTC A G SLC52A2 Ensembl:ENSG00000185803 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144360893..144361156 26863196 MeRIP-seq:(Medium) rs560659799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695874,Human_RBP_ID_18893579,Human_RBP_ID_22776138,Human_RBP_ID_27536851 Clinvar_Rec_256 64912 RMVar_ID_64912 Human_SNP_ID_386258813 m1A Human chr8 + 144374104 144374104 144374104 AGAAGAGCGGAGCAGTGGTCGGAGATGTGGCGACCGGTGAGGACTCTCCCGGCCCGGGGCGCCCG AGAAGAGCGGAGCAGTGGTCGGAGATGTGGCGTCCGGTGAGGACTCTCCCGGCCCGGGGCGCCCG A T ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144374077..144374180 26863196 MeRIP-seq:(Medium) rs200435576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995816 Human_Splice_Rec_1023859,Human_Splice_Rec_1023871,Human_Splice_Rec_1023897,Human_Splice_Rec_1023925,Human_Splice_Rec_1023929,Human_Splice_Rec_1023937 64913 RMVar_ID_64913 Human_SNP_ID_386259414 m1A Human chr8 + 144376363 144376363 144376363 TAAGTTGACAGTCACGCTGGTGTGTGATGAGGACAGTGGCAGGATAGGACCACGGTGAACAAGGT TAAGTTGACAGTCACGCTGGTGTGTGATGAGGCCAGTGGCAGGATAGGACCACGGTGAACAAGGT A C ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144376362..144376440 26863196 MeRIP-seq:(Medium) rs1459651226 Functional Loss SNV dbSNP153 33..33 33 - - - 64914 RMVar_ID_64914 Human_SNP_ID_386259415 m1A Human chr8 + 144376363 144376363 144376363 TAAGTTGACAGTCACGCTGGTGTGTGATGAGGACAGTGGCAGGATAGGACCACGGTGAACAAGGT TAAGTTGACAGTCACGCTGGTGTGTGATGAGGGCAGTGGCAGGATAGGACCACGGTGAACAAGGT A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144376362..144376440 26863196 MeRIP-seq:(Medium) rs1459651226 Functional Loss SNV dbSNP153 33..33 33 - - - 64915 RMVar_ID_64915 Human_SNP_ID_386260146 m1A Human chr8 + 144379468 144379468 144379468 CCTGGCCGTCCCCTGCTGTGTTCTTCAGGAGAAACGTCAGGGGCCTTCCTCCAAGGTAACGAGTC CCTGGCCGTCCCCTGCTGTGTTCTTCAGGAGATACGTCAGGGGCCTTCCTCCAAGGTAACGAGTC A T ADCK5 Ensembl:ENSG00000173137 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144379435..144379535 26863196 MeRIP-seq:(Medium) rs782400800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19022387 Human_Splice_Rec_1023838,Human_Splice_Rec_1023839,Human_Splice_Rec_1023846,Human_Splice_Rec_1023847,Human_Splice_Rec_1023862,Human_Splice_Rec_1023863,Human_Splice_Rec_1023872,Human_Splice_Rec_1023873,Human_Splice_Rec_1023898,Human_Splice_Rec_1023899,Human_Splice_Rec_1023928,Human_Splice_Rec_1023930,Human_Splice_Rec_1023931,Human_Splice_Rec_1023938,Human_Splice_Rec_1023939 RMVar_hsa_circ_9504 64916 RMVar_ID_64916 Human_SNP_ID_386266083 m1A Human chr8 + 144395322 144395322 144395322 CTCCTCGCCAGTCATGCGTGGGATGCGGGCACACGGCGTGTTGGTGCTGGTGGCCACAGCATACA CTCCTCGCCAGTCATGCGTGGGATGCGGGCACGCGGCGTGTTGGTGCTGGTGGCCACAGCATACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144395276..144395375 26863196 MeRIP-seq:(Medium) rs1222441007 Functional Loss SNV dbSNP153 33..33 33 - - - 64917 RMVar_ID_64917 Human_SNP_ID_386266185 m1A Human chr8 - 144395553 144395553 144395553 CCTGGATCCCCTGACCCCTGTGCCCCCACCCCAGGGCGAGCTGAGGATCAGTGTCCTGCCTGCCT CCTGGATCCCCTGACCCCTGTGCCCCCACCCCCGGGCGAGCTGAGGATCAGTGTCCTGCCTGCCT T G CPSF1 Ensembl:ENSG00000071894 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144395426..144395575 26863196 MeRIP-seq:(Medium) rs1415588270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22555687,Human_RBP_ID_22688707,Human_RBP_ID_22747491 RMVar_hsa_circ_117621,RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_255107,RMVar_hsa_circ_97961,RMVar_hsa_circ_102627,RMVar_hsa_circ_255114,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 64918 RMVar_ID_64918 Human_SNP_ID_386266396 m1A Human chr8 - 144396230 144396230 144396230 GGCTCCACCCTGAGGACCAGGAAGGAGTGTCCAGAGGGCGATGGGGTTGAGGTCGAGGAGGTGGA GGCTCCACCCTGAGGACCAGGAAGGAGTGTCCCGAGGGCGATGGGGTTGAGGTCGAGGAGGTGGA T G CPSF1 Ensembl:ENSG00000071894 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144396222..144396330 26863196 MeRIP-seq:(Medium) rs1442922691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87946,Human_RBP_ID_218126,Human_RBP_ID_957979,Human_RBP_ID_3973532,Human_RBP_ID_5329398,Human_RBP_ID_5405133,Human_RBP_ID_8221810,Human_RBP_ID_18427085,Human_RBP_ID_18472629,Human_RBP_ID_19140612,Human_RBP_ID_21655594,Human_RBP_ID_21995694,Human_RBP_ID_22367659,Human_RBP_ID_22419284,Human_RBP_ID_22688708,Human_RBP_ID_22747683,Human_RBP_ID_23259454,Human_RBP_ID_26359558 RMVar_hsa_circ_117621,RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_255107,RMVar_hsa_circ_97961,RMVar_hsa_circ_102627,RMVar_hsa_circ_255114,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 64919 RMVar_ID_64919 Human_SNP_ID_386266397 m1A Human chr8 - 144396237 144396237 144396237 GACCATTGGCTCCACCCTGAGGACCAGGAAGGAGTGTCCAGAGGGCGATGGGGTTGAGGTCGAGG GACCATTGGCTCCACCCTGAGGACCAGGAAGGCGTGTCCAGAGGGCGATGGGGTTGAGGTCGAGG T G CPSF1 Ensembl:ENSG00000071894 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144396216..144396341 26863196 MeRIP-seq:(Medium) rs1280712445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87946,Human_RBP_ID_218126,Human_RBP_ID_957979,Human_RBP_ID_3973532,Human_RBP_ID_5329398,Human_RBP_ID_5405133,Human_RBP_ID_8221810,Human_RBP_ID_18427120,Human_RBP_ID_19140613,Human_RBP_ID_21655594,Human_RBP_ID_21995694,Human_RBP_ID_22367659,Human_RBP_ID_22419285,Human_RBP_ID_22688708,Human_RBP_ID_22747683,Human_RBP_ID_23259454,Human_RBP_ID_26359558 RMVar_hsa_circ_117621,RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_255107,RMVar_hsa_circ_97961,RMVar_hsa_circ_102627,RMVar_hsa_circ_255114,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 64920 RMVar_ID_64920 Human_SNP_ID_386266795 m1A Human chr8 - 144396925 144396925 144396925 TCCCCCATGGCTCCCCTCATCCTGCCAGGTGCATGTGGACCAAGAGCTGCTTATCTACGAGGCCT TCCCCCATGGCTCCCCTCATCCTGCCAGGTGCCTGTGGACCAAGAGCTGCTTATCTACGAGGCCT T G CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144396876..144396950 32194978 MeRIP-seq:(Medium) rs1554864075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1024012,Human_Splice_Rec_1024013,Human_Splice_Rec_1024084,Human_Splice_Rec_1024085 RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_97961,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 64921 RMVar_ID_64921 Human_SNP_ID_386266994 m1A Human chr8 - 144397203 144397203 144397203 GCAGCCGCCAGAGCAGGCCCTACCTGCTGGTGAGTGCGCCTGGCCTGGCCTCCCCTTCCCATCTT GCAGCCGCCAGAGCAGGCCCTACCTGCTGGTGTGTGCGCCTGGCCTGGCCTCCCCTTCCCATCTT T A CPSF1 Ensembl:ENSG00000071894 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144397201..144397375 32194978 MeRIP-seq:(Medium) rs1305696793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_97961,RMVar_hsa_circ_255116 64922 RMVar_ID_64922 Human_SNP_ID_386267170 m1A Human chr8 - 144397623 144397623 144397623 AGTGGATGACGAGGAGGAGATGCTGTATGGGGATTCGGGCTCCCTCTTCAGCCCCAGCAAGGAGG AGTGGATGACGAGGAGGAGATGCTGTATGGGGGTTCGGGCTCCCTCTTCAGCCCCAGCAAGGAGG T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144397601..144397625 26863196 MeRIP-seq:(Medium) rs190438003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958327,Human_RBP_ID_3973534,Human_RBP_ID_8152432,Human_RBP_ID_9312440,Human_RBP_ID_18114148,Human_RBP_ID_19023431 Human_Splice_Rec_1024008,Human_Splice_Rec_1024080 RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_97961,RMVar_hsa_circ_255116,RMVar_hsa_circ_44645 64923 RMVar_ID_64923 Human_SNP_ID_386267313 m1A Human chr8 + 144397876 144397876 144397876 GTCTCGGTACAGGCACAGCGTAATCACCTTGGACTGCTGCGGGGAGAGGGGTGGGCTCAGCGGCG GTCTCGGTACAGGCACAGCGTAATCACCTTGGTCTGCTGCGGGGAGAGGGGTGGGCTCAGCGGCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144397851..144397875 26863196 MeRIP-seq:(Medium) rs1554864644 Functional Loss SNV dbSNP153 33..33 33 - - - 64924 RMVar_ID_64924 Human_SNP_ID_386267405 m1A Human chr8 - 144398055 144398055 144398055 TGCAGTGCGCCGTGGCCGACCCCTATGTGGTCATCATGAGTGCCGAGGGCCACGTCACCATGTTC TGCAGTGCGCCGTGGCCGACCCCTATGTGGTCGTCATGAGTGCCGAGGGCCACGTCACCATGTTC T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144398004..144398359 26863196 MeRIP-seq:(Medium) rs782466045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338529,Human_RBP_ID_18114149 Human_Splice_Rec_1024004,Human_Splice_Rec_1024076 Human_miRNA_ID_2426948,Human_miRNA_ID_2617489 RMVar_hsa_circ_51879 64925 RMVar_ID_64925 Human_SNP_ID_386267594 m1A Human chr8 - 144398362 144398362 144398362 CCACTCAGGGCCCCACGGTCTTTGCTGGGAACATCGGGGACAACCGCTACATTGTCCAAGTGTCA CCACTCAGGGCCCCACGGTCTTTGCTGGGAACGTCGGGGACAACCGCTACATTGTCCAAGTGTCA T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:144398326..144398550 26863196 MeRIP-seq:(Medium) rs782332969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268333,Human_RBP_ID_1694139,Human_RBP_ID_3973538,Human_RBP_ID_27536866 Human_Splice_Rec_1024002,Human_Splice_Rec_1024003,Human_Splice_Rec_1024074,Human_Splice_Rec_1024075 64926 RMVar_ID_64926 Human_SNP_ID_386267606 m1A Human chr8 - 144398392 144398392 144398392 AGATCATGGAGCTGGACACCAGTGGCTTCGCCACTCAGGGCCCCACGGTCTTTGCTGGGAACATC AGATCATGGAGCTGGACACCAGTGGCTTCGCCTCTCAGGGCCCCACGGTCTTTGCTGGGAACATC T A CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144398307..144398393 26863196 MeRIP-seq:(Medium) rs1554864934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_315782,Human_RBP_ID_3973538,Human_RBP_ID_19023436,Human_RBP_ID_23088068,Human_RBP_ID_23216221 Human_Splice_Rec_1024002,Human_Splice_Rec_1024003,Human_Splice_Rec_1024074,Human_Splice_Rec_1024075 64927 RMVar_ID_64927 Human_SNP_ID_386267749 m1A Human chr8 - 144398637 144398637 144398637 CTTCCAGCCTGCCCCCCTTTGGCCCTGACAGGAGGACAATCCCAAGGGGGAGGGCACAGAGCAGG CTTCCAGCCTGCCCCCCTTTGGCCCTGACAGGGGGACAATCCCAAGGGGGAGGGCACAGAGCAGG T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144398526..144398650 26863196 MeRIP-seq:(Medium) rs782755081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795338,Human_RBP_ID_5123700,Human_RBP_ID_18196838,Human_RBP_ID_26360278 Human_Splice_Rec_1024000,Human_Splice_Rec_1024072,Human_Splice_Rec_1024150 64928 RMVar_ID_64928 Human_SNP_ID_386267844 m1A Human chr8 + 144398813 144398812 144398814 CCTCCTTACGCACCGGGGCGATGACTGTCCACATGTCATAGCAGCCGGGAAGCTCAAAGGTTGTC CCTCCTTACGCACCGGGGCGATGACTGTCCAC__GTCATAGCAGCCGGGAAGCTCAAAGGTTGTC CAT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144398801..144398850 32194978 MeRIP-seq:(Medium) rs782230619 Functional Loss DEL dbSNP153 33..34 33 - - - 64929 RMVar_ID_64929 Human_SNP_ID_386267845 m1A Human chr8 + 144398813 144398813 144398813 CCTCCTTACGCACCGGGGCGATGACTGTCCACATGTCATAGCAGCCGGGAAGCTCAAAGGTTGTC CCTCCTTACGCACCGGGGCGATGACTGTCCACGTGTCATAGCAGCCGGGAAGCTCAAAGGTTGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144398801..144398850 32194978 MeRIP-seq:(Medium) rs199994715 Functional Loss SNV dbSNP153 33..33 33 - - - 64930 RMVar_ID_64930 Human_SNP_ID_386267864 m1A Human chr8 - 144398865 144398865 144398865 ATCACACCCCCACCCCATCATCATTCTAGAAGAGCATCCGGCCCCAGGTGGTGACAACCTTTGAG ATCACACCCCCACCCCATCATCATTCTAGAAGGGCATCCGGCCCCAGGTGGTGACAACCTTTGAG T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144398855..144398968 26863196 MeRIP-seq:(Medium) rs1554865229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8923700,Human_RBP_ID_9313746 Human_Splice_Rec_1023998,Human_Splice_Rec_1023999,Human_Splice_Rec_1024070,Human_Splice_Rec_1024071,Human_Splice_Rec_1024148,Human_Splice_Rec_1024149 64931 RMVar_ID_64931 Human_SNP_ID_386269241 m1A Human chr8 - 144401501 144401501 144401501 TTGCTGCCTCCTTCTCCTTCTTTGGCAACGTCATGTCCATGGCCAGCGTGCAGCTGGCAGGAGCC TTGCTGCCTCCTTCTCCTTCTTTGGCAACGTCCTGTCCATGGCCAGCGTGCAGCTGGCAGGAGCC T G CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144401476..144401500 32194978 MeRIP-seq:(Medium) rs1554867167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18893597 Human_Splice_Rec_1023972,Human_Splice_Rec_1023973,Human_Splice_Rec_1024044,Human_Splice_Rec_1024045,Human_Splice_Rec_1024134,Human_Splice_Rec_1024135,Human_Splice_Rec_1024162,Human_Splice_Rec_1024163 Human_miRNA_ID_2393001 64932 RMVar_ID_64932 Human_SNP_ID_386274359 m1A Human chr8 + 144415742 144415742 144415742 AGGCCCCCAGGCTCCCCGAAGGCTTTGCAGCCAGGCCGGGTCCCATGGGCCGTGGGACCCTCCTC AGGCCCCCAGGCTCCCCGAAGGCTTTGCAGCCCGGCCGGGTCCCATGGGCCGTGGGACCCTCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144415738..144415843 26863196 MeRIP-seq:(Medium) rs1554873745 Functional Loss SNV dbSNP153 33..33 33 - - - 64933 RMVar_ID_64933 Human_SNP_ID_386277686 m1A Human chr8 - 144424282 144424282 144424282 CCCGCACCCGTGGACACGCGAGCCTCATGTGCACACCTGCCCCCAGCTCTTCATCACGGTCATGG CCCGCACCCGTGGACACGCGAGCCTCATGTGCGCACCTGCCCCCAGCTCTTCATCACGGTCATGG T C VPS28 Ensembl:ENSG00000160948 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144424276..144424425 26863196 MeRIP-seq:(Medium) rs1564717477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1024269,Human_Splice_Rec_1024283,Human_Splice_Rec_1024301,Human_Splice_Rec_1024319,Human_Splice_Rec_1024331,Human_Splice_Rec_1024339,Human_Splice_Rec_1024351,Human_Splice_Rec_1024363,Human_Splice_Rec_1024375,Human_Splice_Rec_1024393,Human_Splice_Rec_1024411 Human_miRNA_ID_1360885 RMVar_hsa_circ_95075,RMVar_hsa_circ_84676,RMVar_hsa_circ_89172,RMVar_hsa_circ_255128,RMVar_hsa_circ_255129,RMVar_hsa_circ_255127 64934 RMVar_ID_64934 Human_SNP_ID_386278383 m1A Human chr8 - 144425994 144425992 144425994 AGTAAGTCCAGGCGCCCAGGCTGTCCCAACACACCCATGCGCATCTGGCTGCCCTGGGGCAGCCC AGTAAGTCCAGGCGCCCAGGCTGTCCCAACAC__CCATGCGCATCTGGCTGCCCTGGGGCAGCCC GGT G VPS28 Ensembl:ENSG00000160948 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144425991..144426108 26863196 MeRIP-seq:(Medium) rs1229064516 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5090864,Human_RBP_ID_19142106 Human_Splice_Rec_1024260,Human_Splice_Rec_1024274,Human_Splice_Rec_1024292,Human_Splice_Rec_1024310,Human_Splice_Rec_1024326,Human_Splice_Rec_1024356,Human_Splice_Rec_1024357,Human_Splice_Rec_1024370,Human_Splice_Rec_1024384,Human_Splice_Rec_1024402,Human_Splice_Rec_1024424,Human_Splice_Rec_1024432 RMVar_hsa_circ_24374,RMVar_hsa_circ_95075,RMVar_hsa_circ_84676,RMVar_hsa_circ_255128,RMVar_hsa_circ_255127,RMVar_hsa_circ_77287,RMVar_hsa_circ_255131 64935 RMVar_ID_64935 Human_SNP_ID_386278810 m1A Human chr8 - 144426981 144426981 144426981 CCATCTTTGAGTCGGCCCTGGCTCTGCTCCCCAGGTCTCAGTGCTGTGCCCCCCCCAGAGCCTAG CCATCTTTGAGTCGGCCCTGGCTCTGCTCCCCCGGTCTCAGTGCTGTGCCCCCCCCAGAGCCTAG T G VPS28 Ensembl:ENSG00000160948 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144426858..144427000 26863196 MeRIP-seq:(Medium) rs1387957407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4998751,Human_RBP_ID_16381748,Human_RBP_ID_22555898,Human_RBP_ID_22836615 Human_Splice_Rec_1024257,Human_Splice_Rec_1024271,Human_Splice_Rec_1024285,Human_Splice_Rec_1024289,Human_Splice_Rec_1024307,Human_Splice_Rec_1024323,Human_Splice_Rec_1024335,Human_Splice_Rec_1024353,Human_Splice_Rec_1024367,Human_Splice_Rec_1024381,Human_Splice_Rec_1024399,Human_Splice_Rec_1024413,Human_Splice_Rec_1024421,Human_Splice_Rec_1024429 RMVar_hsa_circ_84676,RMVar_hsa_circ_255127 64936 RMVar_ID_64936 Human_SNP_ID_386279165 m1A Human chr8 + 144427947 144427947 144427947 AGGAGGAGCGGGCCTGGCGGGCAGGCGCAGGAAGCTCTCGGTGGAGAGGCCCGGGAGAGCAGCGC AGGAGGAGCGGGCCTGGCGGGCAGGCGCAGGAGGCTCTCGGTGGAGAGGCCCGGGAGAGCAGCGC A G TONSL-AS1 RNACentral:URS00009B4A70 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144427943..144428151 26863196 MeRIP-seq:(Medium) rs1185527094 Functional Loss SNV dbSNP153 33..33 33 - - - 64937 RMVar_ID_64937 Human_SNP_ID_386279175 m1A Human chr8 + 144427997 144427997 144427997 CCGGGAGAGCAGCGCTGAGCCGGCTAACTGGGAGTGGACGGTGCTACCGGGGATGGGAGAAGAGC CCGGGAGAGCAGCGCTGAGCCGGCTAACTGGGTGTGGACGGTGCTACCGGGGATGGGAGAAGAGC A T TONSL-AS1,TONSL-AS1:2 RNACentral:URS00008C1E86,RNACentral:URS00009B4A70 lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144427994..144428094 26863196 MeRIP-seq:(Medium) rs1272600547 Functional Loss SNV dbSNP153 33..33 33 - - - 64938 RMVar_ID_64938 Human_SNP_ID_386280780 m1A Human chr8 - 144432319 144432319 144432319 CAGCTCCGTGGCAGCCGGCAAGGGTGATTCGGACCTCATGGAGCCTGTATTCCGATACCTGGCCA CAGCTCCGTGGCAGCCGGCAAGGGTGATTCGGCCCTCATGGAGCCTGTATTCCGATACCTGGCCA T G TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144432306..144432387 26863196 MeRIP-seq:(Medium) rs1483170008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695931,Human_RBP_ID_959652,Human_RBP_ID_16381828,Human_RBP_ID_18893644,Human_RBP_ID_22836622 Human_Splice_Rec_1024461,Human_Splice_Rec_1024509 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133 64939 RMVar_ID_64939 Human_SNP_ID_386282111 m1A Human chr8 - 144435836 144435836 144435836 CAACCGCAGGCCCAGTAGTACCTCTGGGTCGGACAGTGAGGAGAGCAGGCCCCGTGCCCGAGCCA CAACCGCAGGCCCAGTAGTACCTCTGGGTCGGGCAGTGAGGAGAGCAGGCCCCGTGCCCGAGCCA T C TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:144435801..144435950;chr8:144435801..144436075 26863196 MeRIP-seq:(Medium) rs1564729474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1694159,Human_RBP_ID_5534446,Human_RBP_ID_8917363,Human_RBP_ID_9314171,Human_RBP_ID_16381832 RMVar_hsa_circ_63569,RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_51157,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_255137 64940 RMVar_ID_64940 Human_SNP_ID_386282323 m1A Human chr8 - 144436190 144436190 144436190 AGCCAGCAGCAGCAGCAGCTCAGAAGGCGAGGACAGCGCAGGCCCCGCACGGCCGTCCCAGAAGA AGCCAGCAGCAGCAGCAGCTCAGAAGGCGAGGCCAGCGCAGGCCCCGCACGGCCGTCCCAGAAGA T G TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144436141..144436413 26863196 MeRIP-seq:(Medium) rs1295084168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959658 RMVar_hsa_circ_63569,RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_51157,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_255137 64941 RMVar_ID_64941 Human_SNP_ID_386283312 m1A Human chr8 - 144438729 144438727 144438730 CTGGGGTGGGCTTGGCTCTGTTCCAGAGGACGACACCGATGGCCTGACCCCGCAGCTGGAGGAGG CTGGGGTGGGCTTGGCTCTGTTCCAGAGGAC___ACCGATGGCCTGACCCCGCAGCTGGAGGAGG TGTC T TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144438651..144439924 26863196 MeRIP-seq:(Medium) rs778043482 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3974367,Human_RBP_ID_19023487,Human_RBP_ID_26360288 Human_Splice_Rec_1024442,Human_Splice_Rec_1024443,Human_Splice_Rec_1024488,Human_Splice_Rec_1024489,Human_Splice_Rec_1024528,Human_Splice_Rec_1024529 RMVar_hsa_circ_63569,RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_24346,RMVar_hsa_circ_255139 64942 RMVar_ID_64942 Human_SNP_ID_386283313 m1A Human chr8 - 144438729 144438729 144438729 CTGGGGTGGGCTTGGCTCTGTTCCAGAGGACGACACCGATGGCCTGACCCCGCAGCTGGAGGAGG CTGGGGTGGGCTTGGCTCTGTTCCAGAGGACGGCACCGATGGCCTGACCCCGCAGCTGGAGGAGG T C TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144438651..144439924 26863196 MeRIP-seq:(Medium) rs775263035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974367,Human_RBP_ID_19023487,Human_RBP_ID_26360288 Human_Splice_Rec_1024442,Human_Splice_Rec_1024443,Human_Splice_Rec_1024488,Human_Splice_Rec_1024489,Human_Splice_Rec_1024528,Human_Splice_Rec_1024529 RMVar_hsa_circ_63569,RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_24346,RMVar_hsa_circ_255139 64943 RMVar_ID_64943 Human_SNP_ID_386283508 m1A Human chr8 - 144439458 144439457 144439458 GCCTGTCCATGAGGCCTGTTGGGGGGTGTTCCAGGGAAGGCTGTGACTTCAGCTCTGAACTCGAG GCCTGTCCATGAGGCCTGTTGGGGGGTGTTCC_GGGAAGGCTGTGACTTCAGCTCTGAACTCGAG CT C TONSL Ensembl:ENSG00000160949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144439452..144439605 26863196 MeRIP-seq:(Medium) rs746251860 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8221815,Human_RBP_ID_9441066,Human_RBP_ID_21995708,Human_RBP_ID_22625916 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64944 RMVar_ID_64944 Human_SNP_ID_386283511 m1A Human chr8 - 144439458 144439458 144439458 GCCTGTCCATGAGGCCTGTTGGGGGGTGTTCCAGGGAAGGCTGTGACTTCAGCTCTGAACTCGAG GCCTGTCCATGAGGCCTGTTGGGGGGTGTTCCGGGGAAGGCTGTGACTTCAGCTCTGAACTCGAG T C TONSL Ensembl:ENSG00000160949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144439452..144439605 26863196 MeRIP-seq:(Medium) rs1436925471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8221815,Human_RBP_ID_9441066,Human_RBP_ID_21995708,Human_RBP_ID_22625916 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64945 RMVar_ID_64945 Human_SNP_ID_386283708 m1A Human chr8 - 144440050 144440050 144440050 GGCGGCAGCCACAGCGGAGAGCGAAGCCCTGGAGGCCGGCGAGGTGGAGCTCTCAGAGGGCGGTG GGCGGCAGCCACAGCGGAGAGCGAAGCCCTGGGGGCCGGCGAGGTGGAGCTCTCAGAGGGCGGTG T C TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144440026..144440100 26863196 MeRIP-seq:(Medium) rs778401758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254957,Human_RBP_ID_845616,Human_RBP_ID_959662,Human_RBP_ID_3973567,Human_RBP_ID_8923367,Human_RBP_ID_9405913,Human_RBP_ID_18472593,Human_RBP_ID_19022443,Human_RBP_ID_23088011,Human_RBP_ID_24555271,Human_RBP_ID_26359569 Human_Splice_Rec_1024441,Human_Splice_Rec_1024487,Human_Splice_Rec_1024527 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64946 RMVar_ID_64946 Human_SNP_ID_386283720 m1A Human chr8 - 144440072 144440072 144440072 ATGAGGAGGAGGAGGCGGAGGAGGCGGCAGCCACAGCGGAGAGCGAAGCCCTGGAGGCCGGCGAG ATGAGGAGGAGGAGGCGGAGGAGGCGGCAGCCGCAGCGGAGAGCGAAGCCCTGGAGGCCGGCGAG T C TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144439990..144440200;chr8:144439988..144440150 26863196 MeRIP-seq:(Medium) rs1203932874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254957,Human_RBP_ID_845616,Human_RBP_ID_961100,Human_RBP_ID_3973567,Human_RBP_ID_8923367,Human_RBP_ID_9405913,Human_RBP_ID_18472593,Human_RBP_ID_19022443,Human_RBP_ID_22836640,Human_RBP_ID_23084117,Human_RBP_ID_24555271,Human_RBP_ID_26359569 Human_Splice_Rec_1024441,Human_Splice_Rec_1024487,Human_Splice_Rec_1024527 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64947 RMVar_ID_64947 Human_SNP_ID_386283721 m1A Human chr8 - 144440072 144440072 144440072 ATGAGGAGGAGGAGGCGGAGGAGGCGGCAGCCACAGCGGAGAGCGAAGCCCTGGAGGCCGGCGAG ATGAGGAGGAGGAGGCGGAGGAGGCGGCAGCCCCAGCGGAGAGCGAAGCCCTGGAGGCCGGCGAG T G TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144439990..144440200;chr8:144439988..144440150 26863196 MeRIP-seq:(Medium) rs1203932874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254957,Human_RBP_ID_845616,Human_RBP_ID_961100,Human_RBP_ID_3973567,Human_RBP_ID_8923367,Human_RBP_ID_9405913,Human_RBP_ID_18472593,Human_RBP_ID_19022443,Human_RBP_ID_22836640,Human_RBP_ID_23084117,Human_RBP_ID_24555271,Human_RBP_ID_26359569 Human_Splice_Rec_1024441,Human_Splice_Rec_1024487,Human_Splice_Rec_1024527 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64948 RMVar_ID_64948 Human_SNP_ID_386283843 m1A Human chr8 - 144440338 144440338 144440338 CCCAGCGTCCCCAGCTGCAGGTGCGAGAGCCCATCCCACCCATACTGGCTCCCCGGTGAGCCCAG CCCAGCGTCCCCAGCTGCAGGTGCGAGAGCCCGTCCCACCCATACTGGCTCCCCGGTGAGCCCAG T C TONSL Ensembl:ENSG00000160949 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144440336..144440470 26863196 MeRIP-seq:(Medium) rs749236090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19142126 RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_255132,RMVar_hsa_circ_118426,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_255139 64949 RMVar_ID_64949 Human_SNP_ID_386283900 m1A Human chr8 + 144440464 144440464 144440464 GGCCTCCTCGCGGGACAGTGCAATGTTCAGCCAGGTCTTGGCCTCCTGGAGCAGGAGGAAGGACA GGCCTCCTCGCGGGACAGTGCAATGTTCAGCCGGGTCTTGGCCTCCTGGAGCAGGAGGAAGGACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144440338..144440484 26863196 MeRIP-seq:(Medium) rs1443513113 Functional Loss SNV dbSNP153 33..33 33 - - - 64950 RMVar_ID_64950 Human_SNP_ID_386284127 m1A Human chr8 + 144441016 144441016 144441016 AGCTGCCCTGGGAAAGTCTCCTGCCTTGGAGAAGAGGTCCCCTAGCTGCTCACAGATGACCATGG AGCTGCCCTGGGAAAGTCTCCTGCCTTGGAGAGGAGGTCCCCTAGCTGCTCACAGATGACCATGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144440730..144441048 26863196 MeRIP-seq:(Medium) rs1448754777 Functional Loss SNV dbSNP153 33..33 33 - - - 64951 RMVar_ID_64951 Human_SNP_ID_386284824 m1A Human chr8 - 144442808 144442808 144442808 GAAGTGGCTGAGTGTTTGGGGGGGTATCTTCCAGGGACACTGGCCCAGGGAGAGCTGAATGAGAT GAAGTGGCTGAGTGTTTGGGGGGGTATCTTCCGGGGACACTGGCCCAGGGAGAGCTGAATGAGAT T C TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr8:144442758..144442830;chr8:144442066..144442813 26863196,32194978 MeRIP-seq:(Medium) rs1322348194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15012,Human_RBP_ID_88826,Human_RBP_ID_961199,Human_RBP_ID_3973573,Human_RBP_ID_5407112,Human_RBP_ID_16381907,Human_RBP_ID_18893671,Human_RBP_ID_22115272,Human_RBP_ID_22555701,Human_RBP_ID_22627318,Human_RBP_ID_22688732,Human_RBP_ID_22747689,Human_RBP_ID_23088470,Human_RBP_ID_26156716 RMVar_hsa_circ_121664,RMVar_hsa_circ_255132,RMVar_hsa_circ_86507,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_255138,RMVar_hsa_circ_255142,RMVar_hsa_circ_97504,RMVar_hsa_circ_43109 64952 RMVar_ID_64952 Human_SNP_ID_386285241 m1A Human chr8 - 144443973 144443973 144443973 GGAGCAGCACTGGCAGGAGCTGCAGCTTCGGGAGCGCGCTGACGACCCTCTGGGCTGTGCCGTGG GGAGCAGCACTGGCAGGAGCTGCAGCTTCGGGTGCGCGCTGACGACCCTCTGGGCTGTGCCGTGG T A TONSL Ensembl:ENSG00000160949 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144443926..144444000 26863196 MeRIP-seq:(Medium) rs1170557684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845625,Human_RBP_ID_16381920,Human_RBP_ID_18893677,Human_RBP_ID_23088019,Human_RBP_ID_23120814 Human_Splice_Rec_1024470,Human_Splice_Rec_1024471 RMVar_hsa_circ_121664,RMVar_hsa_circ_255132,RMVar_hsa_circ_86507,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_255138 64953 RMVar_ID_64953 Human_SNP_ID_386287693 m1A Human chr8 - 144450232 144450232 144450232 GAACAAACGAAGCCAACACAGGGCAAGTCTGCATGCGTGCGCGACGGGGCCCCCGCCTCCGGCTC GAACAAACGAAGCCAACACAGGGCAAGTCTGCGTGCGTGCGCGACGGGGCCCCCGCCTCCGGCTC T C CYHR1 Ensembl:ENSG00000187954 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144450030..144450231 26863196 MeRIP-seq:(Medium) rs992899948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114211,RMVar_hsa_circ_255143 64954 RMVar_ID_64954 Human_SNP_ID_386288716 m1A Human chr8 + 144453312 144453312 144453312 GGCAGAAGCCACACTCTGAAGGCAGCTCGCTCACGGCTTTCTCCACGGCCAGGTTCCGGCAGCAG GGCAGAAGCCACACTCTGAAGGCAGCTCGCTCGCGGCTTTCTCCACGGCCAGGTTCCGGCAGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144453194..144453400 26863196 MeRIP-seq:(Medium) rs1169079011 Functional Loss SNV dbSNP153 33..33 33 - - - 64955 RMVar_ID_64955 Human_SNP_ID_386292215 m1A Human chr8 + 144462584 144462584 144462584 CCGCCCCGGGCCCGGCTCCGACCCCGACCCCGACCCCGGCCGGCACGGAGCCCGCGGGCCCCGCG CCGCCCCGGGCCCGGCTCCGACCCCGACCCCGCCCCCGGCCGGCACGGAGCCCGCGGGCCCCGCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:144462582..144462824 26863196 MeRIP-seq:(Medium) rs1477125929 Functional Loss SNV dbSNP153 33..33 33 - - - 64956 RMVar_ID_64956 Human_SNP_ID_386292216 m1A Human chr8 + 144462584 144462584 144462584 CCGCCCCGGGCCCGGCTCCGACCCCGACCCCGACCCCGGCCGGCACGGAGCCCGCGGGCCCCGCG CCGCCCCGGGCCCGGCTCCGACCCCGACCCCGGCCCCGGCCGGCACGGAGCCCGCGGGCCCCGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:144462582..144462824 26863196 MeRIP-seq:(Medium) rs1477125929 Functional Loss SNV dbSNP153 33..33 33 - - - 64957 RMVar_ID_64957 Human_SNP_ID_386292308 m1A Human chr8 + 144462813 144462813 144462813 CGCCTCAGTGGGCCCGGCCCGCGCGTAGCCCCACAGCCGCCGCGGCCACCGACCCCGGCACGGCC CGCCTCAGTGGGCCCGGCCCGCGCGTAGCCCCGCAGCCGCCGCGGCCACCGACCCCGGCACGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEK293T,Starvation treatment chr8:144457920..144462875;chr8:144462750..144462844 26863196,26863410 MeRIP-seq:(Medium) rs1157003007 Functional Loss SNV dbSNP153 33..33 33 - - - 64958 RMVar_ID_64958 Human_SNP_ID_386292310 m1A Human chr8 + 144462815 144462815 144462815 CCTCAGTGGGCCCGGCCCGCGCGTAGCCCCACAGCCGCCGCGGCCACCGACCCCGGCACGGCCGC CCTCAGTGGGCCCGGCCCGCGCGTAGCCCCACGGCCGCCGCGGCCACCGACCCCGGCACGGCCGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr8:144462151..144462875;chr8:144462640..144462875;chr8:144462162..144462900 26863196 MeRIP-seq:(Medium) rs1390341838 Functional Loss SNV dbSNP153 33..33 33 - - - 64959 RMVar_ID_64959 Human_SNP_ID_386292326 m1A Human chr8 + 144462832 144462832 144462832 CGCGCGTAGCCCCACAGCCGCCGCGGCCACCGACCCCGGCACGGCCGCCATCTTTGTTTTCGCTG CGCGCGTAGCCCCACAGCCGCCGCGGCCACCGTCCCCGGCACGGCCGCCATCTTTGTTTTCGCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144462138..144462878 26863196 MeRIP-seq:(Medium) rs1283328370 Functional Loss SNV dbSNP153 33..33 33 - - - 64960 RMVar_ID_64960 Human_SNP_ID_386293519 m1A Human chr8 - 144465054 144465054 144465054 TGGCCTCAGGGATCCGGAAAGTCTAGGACTGAACTTCTCCTAACATCCAGTAATGGGGACCTGGA TGGCCTCAGGGATCCGGAAAGTCTAGGACTGATCTTCTCCTAACATCCAGTAATGGGGACCTGGA T A CYHR1 Ensembl:ENSG00000187954 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144465005..144465128 26863196 MeRIP-seq:(Medium) rs763189480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070432,Human_RBP_ID_4995829,Human_RBP_ID_5430305,Human_RBP_ID_5480839,Human_RBP_ID_16382285,Human_RBP_ID_18172579,Human_RBP_ID_18893715,Human_RBP_ID_23088159,Human_RBP_ID_26188897 Human_Splice_Rec_1024558,Human_Splice_Rec_1024574,Human_Splice_Rec_1024578,Human_Splice_Rec_1024584,Human_Splice_Rec_1024588 RMVar_hsa_circ_114211,RMVar_hsa_circ_255143 64961 RMVar_ID_64961 Human_SNP_ID_386293520 m1A Human chr8 - 144465054 144465054 144465054 TGGCCTCAGGGATCCGGAAAGTCTAGGACTGAACTTCTCCTAACATCCAGTAATGGGGACCTGGA TGGCCTCAGGGATCCGGAAAGTCTAGGACTGAGCTTCTCCTAACATCCAGTAATGGGGACCTGGA T C CYHR1 Ensembl:ENSG00000187954 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144465005..144465128 26863196 MeRIP-seq:(Medium) rs763189480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070432,Human_RBP_ID_4995829,Human_RBP_ID_5430305,Human_RBP_ID_5480839,Human_RBP_ID_16382285,Human_RBP_ID_18172579,Human_RBP_ID_18893715,Human_RBP_ID_23088159,Human_RBP_ID_26188897 Human_Splice_Rec_1024558,Human_Splice_Rec_1024574,Human_Splice_Rec_1024578,Human_Splice_Rec_1024584,Human_Splice_Rec_1024588 RMVar_hsa_circ_114211,RMVar_hsa_circ_255143 64962 RMVar_ID_64962 Human_SNP_ID_386293536 m1A Human chr8 - 144465079 144465079 144465079 TCTTCTTCTCCACAGGTGTGTGCAGTGGCCTCAGGGATCCGGAAAGTCTAGGACTGAACTTCTCC TCTTCTTCTCCACAGGTGTGTGCAGTGGCCTCGGGGATCCGGAAAGTCTAGGACTGAACTTCTCC T C CYHR1 Ensembl:ENSG00000187954 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144464977..144465128 26863410 MeRIP-seq:(Medium) rs927385827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070432,Human_RBP_ID_4975441,Human_RBP_ID_16382285,Human_RBP_ID_18172579,Human_RBP_ID_18893715,Human_RBP_ID_22555906,Human_RBP_ID_22688734,Human_RBP_ID_22747698,Human_RBP_ID_23088159,Human_RBP_ID_23259458,Human_RBP_ID_24563522,Human_RBP_ID_26156747 Human_Splice_Rec_1024558,Human_Splice_Rec_1024574,Human_Splice_Rec_1024578,Human_Splice_Rec_1024584,Human_Splice_Rec_1024588 RMVar_hsa_circ_114211,RMVar_hsa_circ_255143 64963 RMVar_ID_64963 Human_SNP_ID_386293537 m1A Human chr8 - 144465079 144465079 144465079 TCTTCTTCTCCACAGGTGTGTGCAGTGGCCTCAGGGATCCGGAAAGTCTAGGACTGAACTTCTCC TCTTCTTCTCCACAGGTGTGTGCAGTGGCCTCCGGGATCCGGAAAGTCTAGGACTGAACTTCTCC T G CYHR1 Ensembl:ENSG00000187954 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144464977..144465128 26863410 MeRIP-seq:(Medium) rs927385827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070432,Human_RBP_ID_4975441,Human_RBP_ID_16382285,Human_RBP_ID_18172579,Human_RBP_ID_18893715,Human_RBP_ID_22555906,Human_RBP_ID_22688734,Human_RBP_ID_22747698,Human_RBP_ID_23088159,Human_RBP_ID_23259458,Human_RBP_ID_24563522,Human_RBP_ID_26156747 Human_Splice_Rec_1024558,Human_Splice_Rec_1024574,Human_Splice_Rec_1024578,Human_Splice_Rec_1024584,Human_Splice_Rec_1024588 RMVar_hsa_circ_114211,RMVar_hsa_circ_255143 64964 RMVar_ID_64964 Human_SNP_ID_386293602 m1A Human chr8 + 144465228 144465228 144465228 GGGAGTGCGGGCCTGGGGAAGAGAGAGCGGCGAGGCGCTGCAGGCCCACGCGGCGGCCTCGGCCT GGGAGTGCGGGCCTGGGGAAGAGAGAGCGGCGCGGCGCTGCAGGCCCACGCGGCGGCCTCGGCCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144465227..144465377 32194978 MeRIP-seq:(Medium) rs776741535 Functional Loss SNV dbSNP153 33..33 33 - - - 64965 RMVar_ID_64965 Human_SNP_ID_386293801 m1A Human chr8 + 144465627 144465627 144465627 TAGGAGCGGGTGGGGTCGGGAGGAGCTCGGGGACCAGAAAACGCTCTGTTTGGGTGGGTGCGTGC TAGGAGCGGGTGGGGTCGGGAGGAGCTCGGGGGCCAGAAAACGCTCTGTTTGGGTGGGTGCGTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144465576..144465702 26863196 MeRIP-seq:(Medium) rs1362561824 Functional Loss SNV dbSNP153 33..33 33 - - - 64966 RMVar_ID_64966 Human_SNP_ID_386293815 m1A Human chr8 - 144465653 144465653 144465653 CGCTCCTTCCAAACCACTATGCCCACGCACGCACCCACCCAAACAGAGCGTTTTCTGGTCCCCGA CGCTCCTTCCAAACCACTATGCCCACGCACGCGCCCACCCAAACAGAGCGTTTTCTGGTCCCCGA T C CYHR1 Ensembl:ENSG00000187954 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144465211..144465699 26863196 MeRIP-seq:(Medium) rs1265725278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1024573 64967 RMVar_ID_64967 Human_SNP_ID_386293920 m1A Human chr8 - 144465867 144465867 144465867 CCGCCCAGGCCCCGCCCCTCGCAGCCACGCCCAGACCCCCCCATCGCATCCTCGCCCAGGCCCCG CCGCCCAGGCCCCGCCCCTCGCAGCCACGCCCCGACCCCCCCATCGCATCCTCGCCCAGGCCCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144465818..144465957 26863196 MeRIP-seq:(Medium) rs891797309 Functional Loss SNV dbSNP153 33..33 33 - - - 64968 RMVar_ID_64968 Human_SNP_ID_386294054 m1A Human chr8 - 144466104 144466104 144466104 CGGAATCCCTCCCACCCTCCGCGTAGTCCCCCACCGCTCCGGTTTCGCGGAGCCTTCAACACGCC CGGAATCCCTCCCACCCTCCGCGTAGTCCCCCCCCGCTCCGGTTTCGCGGAGCCTTCAACACGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144466062..144466227 26863196 MeRIP-seq:(Medium) rs1235590505 Functional Loss SNV dbSNP153 33..33 33 - - - 64969 RMVar_ID_64969 Human_SNP_ID_386294815 m1A Human chr8 + 144467339 144467339 144467339 GCCAGCCCCTCGGGTCCGGCCCCCCTCTCCAGATGGTGAGTAAAGGACAGTAAGTTGAAGAAGAA GCCAGCCCCTCGGGTCCGGCCCCCCTCTCCAGGTGGTGAGTAAAGGACAGTAAGTTGAAGAAGAA A G KIFC2 Ensembl:ENSG00000167702 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144467201..144467350 32194978 MeRIP-seq:(Medium) rs773802755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1024595,Human_Splice_Rec_1024629,Human_Splice_Rec_1024661,Human_Splice_Rec_1024695,Human_Splice_Rec_1024721 RMVar_hsa_circ_17201 64970 RMVar_ID_64970 Human_SNP_ID_386294970 m1A Human chr8 + 144467540 144467540 144467540 CCTTCCCACTTCACCGCAGTCCCAGGCGAGCCACTGGGGGATGAGACCCAGGGACAGCAGCCCCT CCTTCCCACTTCACCGCAGTCCCAGGCGAGCCGCTGGGGGATGAGACCCAGGGACAGCAGCCCCT A G KIFC2 Ensembl:ENSG00000167702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144467489..144467634 26863196 MeRIP-seq:(Medium) rs1271514421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255441,Human_RBP_ID_19022461,Human_RBP_ID_27831654 Human_Splice_Rec_1024596,Human_Splice_Rec_1024597,Human_Splice_Rec_1024630,Human_Splice_Rec_1024631,Human_Splice_Rec_1024662,Human_Splice_Rec_1024663,Human_Splice_Rec_1024696,Human_Splice_Rec_1024697,Human_Splice_Rec_1024722,Human_Splice_Rec_1024725 RMVar_hsa_circ_17201,RMVar_hsa_circ_45557 64971 RMVar_ID_64971 Human_SNP_ID_386295125 m1A Human chr8 - 144467761 144467761 144467761 CCCTGCAGCCTCACCACGCCCAGGCGCAGTCGACCCAACTCCTCCTCCTGCTGTTCCAGCTGCTG CCCTGCAGCCTCACCACGCCCAGGCGCAGTCGGCCCAACTCCTCCTCCTGCTGTTCCAGCTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144467704..144467930 26863196 MeRIP-seq:(Medium) rs775668967 Functional Loss SNV dbSNP153 33..33 33 - - - 64972 RMVar_ID_64972 Human_SNP_ID_386295216 m1A Human chr8 + 144467879 144467879 144467879 CCTCTCCACCAGGGGGCGACGGACTCAGAGAAAAGGGTTCAGCATCTGACTCTGGAGAACGAGGC CCTCTCCACCAGGGGGCGACGGACTCAGAGAAGAGGGTTCAGCATCTGACTCTGGAGAACGAGGC A G KIFC2 Ensembl:ENSG00000167702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144467715..144467987 26863196 MeRIP-seq:(Medium) rs746507517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628886,Human_RBP_ID_18414408,Human_RBP_ID_18472595,Human_RBP_ID_19022464,Human_RBP_ID_21995166,Human_RBP_ID_22627320,Human_RBP_ID_23084137,Human_RBP_ID_26359577,Human_RBP_ID_27831656 Human_Splice_Rec_1024600,Human_Splice_Rec_1024634,Human_Splice_Rec_1024666,Human_Splice_Rec_1024700,Human_Splice_Rec_1024728 RMVar_hsa_circ_45557 64973 RMVar_ID_64973 Human_SNP_ID_386295509 m1A Human chr8 + 144468378 144468378 144468378 GCTAGAGCTCCAGGGCCGGCTTCAGGAGGCCCAAGACACCACAGAAGCCCTCCGAGCCCAGGTGG GCTAGAGCTCCAGGGCCGGCTTCAGGAGGCCCGAGACACCACAGAAGCCCTCCGAGCCCAGGTGG A G KIFC2 Ensembl:ENSG00000167702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144468287..144468469;chr8:144468279..144468445 26863196 MeRIP-seq:(Medium) rs1194532533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958735,Human_RBP_ID_18893717 Human_Splice_Rec_1024602,Human_Splice_Rec_1024603,Human_Splice_Rec_1024636,Human_Splice_Rec_1024637,Human_Splice_Rec_1024668,Human_Splice_Rec_1024669,Human_Splice_Rec_1024702,Human_Splice_Rec_1024703,Human_Splice_Rec_1024724 RMVar_hsa_circ_45557 64974 RMVar_ID_64974 Human_SNP_ID_386295648 m1A Human chr8 + 144468594 144468594 144468594 GGGCCTTCAAGGGGCCCTCCAGCAGCTCCAGCAGGAGACGGAGCAGAACTGCAGGCGTGAGCTAC GGGCCTTCAAGGGGCCCTCCAGCAGCTCCAGCCGGAGACGGAGCAGAACTGCAGGCGTGAGCTAC A C KIFC2 Ensembl:ENSG00000167702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144468545..144468618 26863196 MeRIP-seq:(Medium) rs777784898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268037,Human_RBP_ID_958736,Human_RBP_ID_3885681,Human_RBP_ID_3973584,Human_RBP_ID_4995316,Human_RBP_ID_5329029,Human_RBP_ID_18427087,Human_RBP_ID_19140660,Human_RBP_ID_21995011,Human_RBP_ID_23216223,Human_RBP_ID_27831657 Human_Splice_Rec_1024604,Human_Splice_Rec_1024605,Human_Splice_Rec_1024638,Human_Splice_Rec_1024639,Human_Splice_Rec_1024670,Human_Splice_Rec_1024671,Human_Splice_Rec_1024704,Human_Splice_Rec_1024705 64975 RMVar_ID_64975 Human_SNP_ID_386297864 m1A Human chr8 - 144473255 144473252 144473255 CCCGGTGAGCGGAGTGTCGGTGCTGAGGGAAGAAGGCGTCCCGGAGGAGCGCGGGACCCTGCGGC CCCGGTGAGCGGAGTGTCGGTGCTGAGGGAAG___GCGTCCCGGAGGAGCGCGGGACCCTGCGGC CCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144473205..144473292 26863196 MeRIP-seq:(Medium) rs1451572454 Functional Loss DEL dbSNP153 33..35 33 - - - 64976 RMVar_ID_64976 Human_SNP_ID_386297866 m1A Human chr8 - 144473255 144473255 144473255 CCCGGTGAGCGGAGTGTCGGTGCTGAGGGAAGAAGGCGTCCCGGAGGAGCGCGGGACCCTGCGGC CCCGGTGAGCGGAGTGTCGGTGCTGAGGGAAGGAGGCGTCCCGGAGGAGCGCGGGACCCTGCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144473205..144473292 26863196 MeRIP-seq:(Medium) rs751951972 Functional Loss SNV dbSNP153 33..33 33 - - - 64977 RMVar_ID_64977 Human_SNP_ID_386298044 m1A Human chr8 - 144473499 144473499 144473499 GGTGACTCTGGGAGCTCAGGGGCAATGGATCCAAAGAGGCTAGGGAGCTTGTGCCCTGGGAGACG GGTGACTCTGGGAGCTCAGGGGCAATGGATCCGAAGAGGCTAGGGAGCTTGTGCCCTGGGAGACG T C FOXH1 Ensembl:ENSG00000160973 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144473449..144473749 26863196 MeRIP-seq:(Medium) rs1250382669 Functional Loss SNV dbSNP153 33..33 33 - - - 64978 RMVar_ID_64978 Human_SNP_ID_386298213 m1A Human chr8 - 144473940 144473940 144473940 CTAGTCCCCTCTTCTCAGCCCACTACCCATCCATCAGTCACCAGCCGTCACCTCCCCTCCCGTGC CTAGTCCCCTCTTCTCAGCCCACTACCCATCCTTCAGTCACCAGCCGTCACCTCCCCTCCCGTGC T A FOXH1 Ensembl:ENSG00000160973 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144473890..144474061 26863196 MeRIP-seq:(Medium) rs1421061360 Functional Loss SNV dbSNP153 33..33 33 - - - 64979 RMVar_ID_64979 Human_SNP_ID_386300183 m1A Human chr8 + 144478398 144478398 144478398 GACGCGGCTGCCGGCACGCGGGCGCCCAGGGCACAGGTCCCGCCGGGCCGCCTTGGGCGTTGCTG GACGCGGCTGCCGGCACGCGGGCGCCCAGGGCGCAGGTCCCGCCGGGCCGCCTTGGGCGTTGCTG A G PPP1R16A Ensembl:ENSG00000160972 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144478389..144478516 26863196 MeRIP-seq:(Medium) rs536341315 Functional Loss SNV dbSNP153 33..33 33 - - - 64980 RMVar_ID_64980 Human_SNP_ID_386305395 m1A Human chr8 - 144497084 144497084 144497084 GGGCAGCTAGCTGGACTGGCACCCTCGGGGGCATCCCCTTCCCAGAGCTTCGTGCCCTTGGCTGG GGGCAGCTAGCTGGACTGGCACCCTCGGGGGCTTCCCCTTCCCAGAGCTTCGTGCCCTTGGCTGG T A AC084125.2 Ensembl:ENSG00000255182 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144496442..144497511 32194978 MeRIP-seq:(Medium) rs1298602221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1694202,Human_RBP_ID_5631094 64981 RMVar_ID_64981 Human_SNP_ID_386305404 m1A Human chr8 - 144497108 144497108 144497108 GGGCCAGGCTGGGCCTGAGGGGTGGGGCAGCTAGCTGGACTGGCACCCTCGGGGGCATCCCCTTC GGGCCAGGCTGGGCCTGAGGGGTGGGGCAGCTTGCTGGACTGGCACCCTCGGGGGCATCCCCTTC T A AC084125.2 Ensembl:ENSG00000255182 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144496840..144497453 26863196 MeRIP-seq:(Medium) rs1264002203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5631094 64982 RMVar_ID_64982 Human_SNP_ID_386305405 m1A Human chr8 - 144497108 144497108 144497108 GGGCCAGGCTGGGCCTGAGGGGTGGGGCAGCTAGCTGGACTGGCACCCTCGGGGGCATCCCCTTC GGGCCAGGCTGGGCCTGAGGGGTGGGGCAGCTGGCTGGACTGGCACCCTCGGGGGCATCCCCTTC T C AC084125.2 Ensembl:ENSG00000255182 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144496840..144497453 26863196 MeRIP-seq:(Medium) rs1264002203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5631094 64983 RMVar_ID_64983 Human_SNP_ID_386307238 m1A Human chr8 + 144501233 144501233 144501233 CGTGTGGCAACAGCCGCCGCCCACCAGCCCGGAGCCGCCCGAGGACAACGATGACCGCCAGACAG CGTGTGGCAACAGCCGCCGCCCACCAGCCCGGGGCCGCCCGAGGACAACGATGACCGCCAGACAG A G PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144501122..144501320 26863196 MeRIP-seq:(Medium) rs1354680885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795830,Human_RBP_ID_19023559 Human_Splice_Rec_1024769,Human_Splice_Rec_1024799,Human_Splice_Rec_1024825,Human_Splice_Rec_1024843 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_124529,RMVar_hsa_circ_255152,RMVar_hsa_circ_255153,RMVar_hsa_circ_285951,RMVar_hsa_circ_255154 64984 RMVar_ID_64984 Human_SNP_ID_386307256 m1A Human chr8 - 144501252 144501252 144501252 GGCGGCCTGAGCTCTGCGCCTGTCTGGCGGTCATCGTTGTCCTCGGGCGGCTCCGGGCTGGTGGG GGCGGCCTGAGCTCTGCGCCTGTCTGGCGGTCGTCGTTGTCCTCGGGCGGCTCCGGGCTGGTGGG T C AC084125.2 Ensembl:ENSG00000255182 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144501201..144501294 26863196 MeRIP-seq:(Medium) rs1412202055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633050 64985 RMVar_ID_64985 Human_SNP_ID_386307478 m1A Human chr8 + 144501625 144501625 144501625 AGCGACTAGACCGGAGTGTCTCCTACCAGCTGAGCCCCCTGGACAGCACCACCCCCCACACCCTG AGCGACTAGACCGGAGTGTCTCCTACCAGCTGCGCCCCCTGGACAGCACCACCCCCCACACCCTG A C PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144501576..144501756 26863196 MeRIP-seq:(Medium) rs1483143975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17666053,Human_RBP_ID_27536915 Human_miRNA_ID_2269299 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_255153 64986 RMVar_ID_64986 Human_SNP_ID_386307501 m1A Human chr8 + 144501652 144501652 144501652 AGCTGAGCCCCCTGGACAGCACCACCCCCCACACCCTGGTCCACGACAAGGCCCACCACACCCTG AGCTGAGCCCCCTGGACAGCACCACCCCCCACCCCCTGGTCCACGACAAGGCCCACCACACCCTG A C PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144501602..144501800 26863196 MeRIP-seq:(Medium) rs961726379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17666053,Human_RBP_ID_27536915 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_255153 64987 RMVar_ID_64987 Human_SNP_ID_386307581 m1A Human chr8 + 144501784 144501784 144501784 CTGAGACAGCTGAGCCTGGCCTGCCTGGTGACACGGTGACCCCCCAGCCTGACTGTGGCTTCAGG CTGAGACAGCTGAGCCTGGCCTGCCTGGTGACCCGGTGACCCCCCAGCCTGACTGTGGCTTCAGG A C PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144501518..144501958 26863196 MeRIP-seq:(Medium) rs773480719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845867,Human_RBP_ID_4975519,Human_RBP_ID_5154370 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_255153 64988 RMVar_ID_64988 Human_SNP_ID_386307582 m1A Human chr8 + 144501784 144501784 144501784 CTGAGACAGCTGAGCCTGGCCTGCCTGGTGACACGGTGACCCCCCAGCCTGACTGTGGCTTCAGG CTGAGACAGCTGAGCCTGGCCTGCCTGGTGACTCGGTGACCCCCCAGCCTGACTGTGGCTTCAGG A T PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144501518..144501958 26863196 MeRIP-seq:(Medium) rs773480719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845867,Human_RBP_ID_4975519,Human_RBP_ID_5154370 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_255153 64989 RMVar_ID_64989 Human_SNP_ID_386310053 m1A Human chr8 + 144506899 144506899 144506899 GTCCCGCCACCCTGGCCCTTCACTCACTGTCAACTCCTTTCAGGATGACCATTCTGCCCCCCTTG GTCCCGCCACCCTGGCCCTTCACTCACTGTCAGCTCCTTTCAGGATGACCATTCTGCCCCCCTTG A G GPT Ensembl:ENSG00000167701 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144506763..144506965 26863196 MeRIP-seq:(Medium) rs750130376 Functional Loss SNV dbSNP153 33..33 33 - - - 64990 RMVar_ID_64990 Human_SNP_ID_386310379 m1A Human chr8 - 144507800 144507800 144507800 CATGCTCCCCAGGCCAGGACACAGCGCTGCCCACTCCCGCTCAGCCCAGCCCCTGCCTCCTCCAG CATGCTCCCCAGGCCAGGACACAGCGCTGCCCTCTCCCGCTCAGCCCAGCCCCTGCCTCCTCCAG T A lnc-RECQL4-3 RNACentral:URS00008B468E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144507750..144507818 26863196 MeRIP-seq:(Medium) rs1458898038 Functional Loss SNV dbSNP153 33..33 33 - - - 64991 RMVar_ID_64991 Human_SNP_ID_386310878 m1A Human chr8 + 144509127 144509127 144509127 CGCCGGTGTCCGGACCGCTCGCCCCCGTTTGGACCCGACTTCGGTTCTTCTGGGGTGTTGATGCT CGCCGGTGTCCGGACCGCTCGCCCCCGTTTGGTCCCGACTTCGGTTCTTCTGGGGTGTTGATGCT A T MFSD3 Ensembl:ENSG00000167700 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144509076..144509356 26863196 MeRIP-seq:(Medium) rs1014336629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696000,Human_RBP_ID_1694234,Human_RBP_ID_4975541,Human_RBP_ID_22330009,Human_RBP_ID_24391159 64992 RMVar_ID_64992 Human_SNP_ID_386310890 m1A Human chr8 - 144509156 144509156 144509156 GGTCTGGACACGTGCTCTCGGGCTTTAGGAGCATCAACACCCCAGAAGAACCGAAGTCGGGTCCA GGTCTGGACACGTGCTCTCGGGCTTTAGGAGCGTCAACACCCCAGAAGAACCGAAGTCGGGTCCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144509126..144509375 26863196 MeRIP-seq:(Medium) rs773979889 Functional Loss SNV dbSNP153 33..33 33 - - - 64993 RMVar_ID_64993 Human_SNP_ID_386310970 m1A Human chr8 + 144509317 144509317 144509317 ACCCCACCTGGAACCCGACCTCCCAGCCTCGCAGCCGGCCTGAGCCGCCATGCGCGGGAAGTTGC ACCCCACCTGGAACCCGACCTCCCAGCCTCGCGGCCGGCCTGAGCCGCCATGCGCGGGAAGTTGC A G MFSD3 Ensembl:ENSG00000167700 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144509270..144509763 32194978 MeRIP-seq:(Medium) rs1014625895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996485,Human_RBP_ID_27122861 Human_miRNA_ID_2269300 RMVar_hsa_circ_81257,RMVar_hsa_circ_255155 64994 RMVar_ID_64994 Human_SNP_ID_386311106 m1A Human chr8 - 144509563 144509563 144509563 GCAGCCCGGCAAGCAGCCCACACACCAGGCCCAGGCCCGCCGTGCTGCGCGTCACCCAGGCCCTC GCAGCCCGGCAAGCAGCCCACACACCAGGCCCGGGCCCGCCGTGCTGCGCGTCACCCAGGCCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144509515..144509783 26863196 MeRIP-seq:(Medium) rs976966997 Functional Loss SNV dbSNP153 33..33 33 - - - 64995 RMVar_ID_64995 Human_SNP_ID_386311107 m1A Human chr8 - 144509563 144509563 144509563 GCAGCCCGGCAAGCAGCCCACACACCAGGCCCAGGCCCGCCGTGCTGCGCGTCACCCAGGCCCTC GCAGCCCGGCAAGCAGCCCACACACCAGGCCCCGGCCCGCCGTGCTGCGCGTCACCCAGGCCCTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144509515..144509783 26863196 MeRIP-seq:(Medium) rs976966997 Functional Loss SNV dbSNP153 33..33 33 - - - 64996 RMVar_ID_64996 Human_SNP_ID_386311636 m1A Human chr8 + 144510437 144510437 144510437 ACGGCGTTTCTGCTCCCGAGTTGGGACTGTGGAATGGTGTGGGTGCTGTGGTCTGCTCCATCGCT ACGGCGTTTCTGCTCCCGAGTTGGGACTGTGGCATGGTGTGGGTGCTGTGGTCTGCTCCATCGCT A C MFSD3 Ensembl:ENSG00000167700 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr8:144510386..144510506;chr8:144510386..144510486 26863196,32194978 MeRIP-seq:(Medium) rs757319064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8917371,Human_RBP_ID_24250198 Human_Splice_Rec_1024936,Human_Splice_Rec_1024937,Human_Splice_Rec_1024948 Human_miRNA_ID_2055563 RMVar_hsa_circ_81257,RMVar_hsa_circ_102282,RMVar_hsa_circ_255155,RMVar_hsa_circ_255156 64997 RMVar_ID_64997 Human_SNP_ID_386311747 m1A Human chr8 - 144510639 144510630 144510639 AGACCAAGGCAGTCTGACAGGCTAGGCCCCCGAGGCGGAAGCGCAGCACCGACCTCAACAGAGGC AGACCAAGGCAGTCTGACAGGCTAGGCCCCCG_________CGCAGCACCGACCTCAACAGAGGC GCTTCCGCCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144510601..144511150 26863196 MeRIP-seq:(Medium) rs1242849932 Functional Loss DEL dbSNP153 33..41 33 - - - 64998 RMVar_ID_64998 Human_SNP_ID_386311755 m1A Human chr8 - 144510639 144510639 144510639 AGACCAAGGCAGTCTGACAGGCTAGGCCCCCGAGGCGGAAGCGCAGCACCGACCTCAACAGAGGC AGACCAAGGCAGTCTGACAGGCTAGGCCCCCGGGGCGGAAGCGCAGCACCGACCTCAACAGAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144510601..144511150 26863196 MeRIP-seq:(Medium) rs1564783742 Functional Loss SNV dbSNP153 33..33 33 - - - 64999 RMVar_ID_64999 Human_SNP_ID_386311762 m1A Human chr8 - 144510648 144510648 144510648 CCAGGTGGAAGACCAAGGCAGTCTGACAGGCTAGGCCCCCGAGGCGGAAGCGCAGCACCGACCTC CCAGGTGGAAGACCAAGGCAGTCTGACAGGCTGGGCCCCCGAGGCGGAAGCGCAGCACCGACCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144510603..144510770 26863196 MeRIP-seq:(Medium) rs1457358334 Functional Loss SNV dbSNP153 33..33 33 - - - 65000 RMVar_ID_65000 Human_SNP_ID_386312694 m1A Human chr8 - 144512002 144512002 144512002 GCAGCAGGATGAGGAGCGCAGCACCAGGCTCAAGGACCTGCTCGGCCGCTACTTTGAGGAAGAGG GCAGCAGGATGAGGAGCGCAGCACCAGGCTCACGGACCTGCTCGGCCGCTACTTTGAGGAAGAGG T G RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs772729762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1224022,Human_RBP_ID_9312441,Human_RBP_ID_23087923 Human_Splice_Rec_1024986,Human_Splice_Rec_1024987,Human_Splice_Rec_1025024,Human_Splice_Rec_1025025,Human_Splice_Rec_1025032,Human_Splice_Rec_1025033,Human_Splice_Rec_1025042 RMVar_hsa_circ_76649,RMVar_hsa_circ_92523,RMVar_hsa_circ_119980,RMVar_hsa_circ_255159,RMVar_hsa_circ_255160,RMVar_hsa_circ_255161 65001 RMVar_ID_65001 Human_SNP_ID_386313386 m1A Human chr8 - 144512939 144512939 144512939 CCCCCCTCAAGAGGCTGAGCAGCTTAGCCACCAAGCAGCCCCAGGACCCAGAAGGGTCTGCATGG CCCCCCTCAAGAGGCTGAGCAGCTTAGCCACCGAGCAGCCCCAGGACCCAGAAGGGTCTGCATGG T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144512814..144512984 26863196 MeRIP-seq:(Medium) rs1564792721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21995719,Human_RBP_ID_22330065 Human_Splice_Rec_1024979,Human_Splice_Rec_1025017,Human_Splice_Rec_1025061 Human_miRNA_ID_2039795,Human_miRNA_ID_3018776 Clinvar_Rec_257 65002 RMVar_ID_65002 Human_SNP_ID_386313712 m1A Human chr8 - 144513302 144513301 144513303 GTGCGGGCTGTGCTGCATCTGGGGCTGCCCCCAAGCTTCGAGAGCTACGTGCAGGCCGTGGGCCG GTGCGGGCTGTGCTGCATCTGGGGCTGCCCC__AGCTTCGAGAGCTACGTGCAGGCCGTGGGCCG TTG T RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144513251..144513500 26863196 MeRIP-seq:(Medium) rs566135735 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17172464,Human_RBP_ID_18172732,Human_RBP_ID_18893786 Human_Splice_Rec_1024977,Human_Splice_Rec_1025015 65003 RMVar_ID_65003 Human_SNP_ID_386313713 m1A Human chr8 - 144513302 144513302 144513302 GTGCGGGCTGTGCTGCATCTGGGGCTGCCCCCAAGCTTCGAGAGCTACGTGCAGGCCGTGGGCCG GTGCGGGCTGTGCTGCATCTGGGGCTGCCCCCGAGCTTCGAGAGCTACGTGCAGGCCGTGGGCCG T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144513251..144513500 26863196 MeRIP-seq:(Medium) rs780098660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17172464,Human_RBP_ID_18172732,Human_RBP_ID_18893786 Human_Splice_Rec_1024977,Human_Splice_Rec_1025015 65004 RMVar_ID_65004 Human_SNP_ID_386313719 m1A Human chr8 + 144513309 144513309 144513309 CGGCCTGCACGTAGCTCTCGAAGCTTGGGGGCAGCCCCAGATGCAGCACAGCCCGCACATCTGGC CGGCCTGCACGTAGCTCTCGAAGCTTGGGGGCGGCCCCAGATGCAGCACAGCCCGCACATCTGGC A G AC084125.4 Ensembl:ENSG00000265393 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144513262..144513461 26863196 MeRIP-seq:(Medium) rs774894142 Functional Loss SNV dbSNP153 33..33 33 - - - 65005 RMVar_ID_65005 Human_SNP_ID_386313731 m1A Human chr8 + 144513326 144513326 144513326 TCGAAGCTTGGGGGCAGCCCCAGATGCAGCACAGCCCGCACATCTGGCCGGTCCAGCCCCATCCC TCGAAGCTTGGGGGCAGCCCCAGATGCAGCACGGCCCGCACATCTGGCCGGTCCAGCCCCATCCC A G AC084125.4 Ensembl:ENSG00000265393 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144513276..144513434 26863196 MeRIP-seq:(Medium) rs1554898259 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_258 65006 RMVar_ID_65006 Human_SNP_ID_386313743 m1A Human chr8 - 144513338 144513338 144513338 ACGGTGGCCTTTGGGATGGGGCTGGACCGGCCAGATGTGCGGGCTGTGCTGCATCTGGGGCTGCC ACGGTGGCCTTTGGGATGGGGCTGGACCGGCCGGATGTGCGGGCTGTGCTGCATCTGGGGCTGCC T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr8:144513226..144513725;chr8:144513237..144513401 26863196 MeRIP-seq:(Medium) rs1060504215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3973597,Human_RBP_ID_5135220,Human_RBP_ID_5153980,Human_RBP_ID_5406285,Human_RBP_ID_17172464,Human_RBP_ID_18172732,Human_RBP_ID_22115292 65007 RMVar_ID_65007 Human_SNP_ID_386313942 m1A Human chr8 - 144513597 144513587 144513598 GCGGATCGCTGCGCTCCTCCGAACCTGCCTGCACGCAGCCTGGGTCCCAGGGTCTGGAGGTGCGG GCGGATCGCTGCGCTCCTCCGAACCTGCCTG___________GGTCCCAGGGTCTGGAGGTGCGG CCAGGCTGCGTG C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:144513576..144513625 26863196 MeRIP-seq:(Medium) rs1314513488 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_18893788 Human_Splice_Rec_1024975,Human_Splice_Rec_1025013,Human_Splice_Rec_1025057 65008 RMVar_ID_65008 Human_SNP_ID_386313950 m1A Human chr8 - 144513597 144513597 144513597 GCGGATCGCTGCGCTCCTCCGAACCTGCCTGCACGCAGCCTGGGTCCCAGGGTCTGGAGGTGCGG GCGGATCGCTGCGCTCCTCCGAACCTGCCTGCTCGCAGCCTGGGTCCCAGGGTCTGGAGGTGCGG T A RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:144513576..144513625 26863196 MeRIP-seq:(Medium) rs755481980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18893788 Human_Splice_Rec_1024975,Human_Splice_Rec_1025013,Human_Splice_Rec_1025057 Clinvar_Rec_259 65009 RMVar_ID_65009 Human_SNP_ID_386314200 m1A Human chr8 - 144513840 144513840 144513840 CGACCCCTCCTCACTCCCCACCGCCCACGCCGACCCCTTCTCACTCCCCACCGCCCACGCCGACC CGACCCCTCCTCACTCCCCACCGCCCACGCCGCCCCCTTCTCACTCCCCACCGCCCACGCCGACC T G RECQL4 Ensembl:ENSG00000160957 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr8:144513701..144513900;chr8:144513754..144513934;chr8:144513750..144513912 26863196 MeRIP-seq:(Medium) rs1405675547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135074,Human_RBP_ID_5329416,Human_RBP_ID_17094062,Human_RBP_ID_18961336 65010 RMVar_ID_65010 Human_SNP_ID_386314205 m1A Human chr8 - 144513846 144513846 144513846 CCACGCCGACCCCTCCTCACTCCCCACCGCCCACGCCGACCCCTTCTCACTCCCCACCGCCCACG CCACGCCGACCCCTCCTCACTCCCCACCGCCCTCGCCGACCCCTTCTCACTCCCCACCGCCCACG T A RECQL4 Ensembl:ENSG00000160957 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144513680..144513928 26863196 MeRIP-seq:(Medium) rs1355997154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135074,Human_RBP_ID_5329416,Human_RBP_ID_17094062,Human_RBP_ID_18961336 65011 RMVar_ID_65011 Human_SNP_ID_386314206 m1A Human chr8 - 144513846 144513846 144513846 CCACGCCGACCCCTCCTCACTCCCCACCGCCCACGCCGACCCCTTCTCACTCCCCACCGCCCACG CCACGCCGACCCCTCCTCACTCCCCACCGCCCGCGCCGACCCCTTCTCACTCCCCACCGCCCACG T C RECQL4 Ensembl:ENSG00000160957 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144513680..144513928 26863196 MeRIP-seq:(Medium) rs1355997154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135074,Human_RBP_ID_5329416,Human_RBP_ID_17094062,Human_RBP_ID_18961336 65012 RMVar_ID_65012 Human_SNP_ID_386314665 m1A Human chr8 + 144514423 144514423 144514423 CCAGGTGCCCGCCCGCTGCCTCCCTCACCCCTAGGCCCATGAGGCCCCCACCTTCTGCAGGACAG CCAGGTGCCCGCCCGCTGCCTCCCTCACCCCTGGGCCCATGAGGCCCCCACCTTCTGCAGGACAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144514376..144514535 26863196 MeRIP-seq:(Medium) rs1043491319 Functional Loss SNV dbSNP153 33..33 33 - - - 65013 RMVar_ID_65013 Human_SNP_ID_386314694 m1A Human chr8 - 144514463 144514463 144514463 GCCTGCATACACTCGGGCATGACCAGGAAGCAACGGGAATCTGTCCTGCAGAAGGTGGGGGCCTC GCCTGCATACACTCGGGCATGACCAGGAAGCAGCGGGAATCTGTCCTGCAGAAGGTGGGGGCCTC T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144514022..144514600;chr8:144514071..144514650 26863196 MeRIP-seq:(Medium) rs1332576218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1694244,Human_RBP_ID_3974389,Human_RBP_ID_18452349 Human_Splice_Rec_1024968,Human_Splice_Rec_1024969,Human_Splice_Rec_1025006,Human_Splice_Rec_1025007,Human_Splice_Rec_1025051,Human_Splice_Rec_1025074,Human_Splice_Rec_1025075 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 65014 RMVar_ID_65014 Human_SNP_ID_386315726 m1A Human chr8 + 144516103 144516102 144516103 TGTCATGGCGGGCCAGCCGAGGGAAGATGTGCAGGGGGGCTGTGCCCTCAGCCTTCCCAGCCCTA TGTCATGGCGGGCCAGCCGAGGGAAGATGTGC_GGGGGGCTGTGCCCTCAGCCTTCCCAGCCCTA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144515962..144516142 26863196 MeRIP-seq:(Medium) rs1173293384 Functional Loss DEL dbSNP153 33..33 33 - - - 65015 RMVar_ID_65015 Human_SNP_ID_386315728 m1A Human chr8 + 144516103 144516103 144516103 TGTCATGGCGGGCCAGCCGAGGGAAGATGTGCAGGGGGGCTGTGCCCTCAGCCTTCCCAGCCCTA TGTCATGGCGGGCCAGCCGAGGGAAGATGTGCGGGGGGGCTGTGCCCTCAGCCTTCCCAGCCCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144515962..144516142 26863196 MeRIP-seq:(Medium) rs1554902362 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_260 65016 RMVar_ID_65016 Human_SNP_ID_386315908 m1A Human chr8 - 144516361 144516361 144516361 CCAAGAAGTCAGCATCCGTGTGGGGAGCCCCCAGCCCAGCAGCAGTGGAGGCGAGAAGCGGAGAT CCAAGAAGTCAGCATCCGTGTGGGGAGCCCCCGGCCCAGCAGCAGTGGAGGCGAGAAGCGGAGAT T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144516254..144516477 26863196 MeRIP-seq:(Medium) rs373588660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845422,Human_RBP_ID_4975662,Human_RBP_ID_5123578,Human_RBP_ID_5154371,Human_RBP_ID_9405930,Human_RBP_ID_17672370,Human_RBP_ID_19023585,Human_RBP_ID_22115296,Human_RBP_ID_22419294,Human_RBP_ID_23088165 Human_Splice_Rec_1025084 RMVar_hsa_circ_2708,RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 65017 RMVar_ID_65017 Human_SNP_ID_386316062 m1A Human chr8 + 144516583 144516583 144516583 AGCCAGGATCTAGGGAGCCCAGCCGCTGGCTCAGGGATGCCTGCAGATGCTGGAGCCGGCCTGGC AGCCAGGATCTAGGGAGCCCAGCCGCTGGCTCTGGGATGCCTGCAGATGCTGGAGCCGGCCTGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144516532..144516780 26863196 MeRIP-seq:(Medium) rs753361853 Functional Loss SNV dbSNP153 33..33 33 - - - 65018 RMVar_ID_65018 Human_SNP_ID_386316829 m1A Human chr8 - 144517784 144517784 144517784 GCAAGCGCGGAGGCCGGGCGGGCGCGCGCGCCATGGAGCGGCTGCGGGACGTGCGGGAGCGGCTG GCAAGCGCGGAGGCCGGGCGGGCGCGCGCGCCCTGGAGCGGCTGCGGGACGTGCGGGAGCGGCTG T G RECQL4 Ensembl:ENSG00000160957 Protein coding start codon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr8:144517451..144517850;chr8:144517551..144517825;chr8:144517693..144517814;chr8:144517720..144517808;chr8:144517399..144517875;chr8:144517401..144517875;chr8:144517676..144517850 26863196,26863410,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs964623569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254976,Human_RBP_ID_4975702,Human_RBP_ID_18426775,Human_RBP_ID_23087924 Human_Splice_Rec_1024951 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 65019 RMVar_ID_65019 Human_SNP_ID_386316844 m1A Human chr8 - 144517806 144517806 144517806 GCGGGAGATTCGCTGGACGATCGCAAGCGCGGAGGCCGGGCGGGCGCGCGCGCCATGGAGCGGCT GCGGGAGATTCGCTGGACGATCGCAAGCGCGGGGGCCGGGCGGGCGCGCGCGCCATGGAGCGGCT T C RECQL4 Ensembl:ENSG00000160957 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:144517723..144517809 26863410 MeRIP-seq:(Medium) rs1270450461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254976,Human_RBP_ID_4995834,Human_RBP_ID_9338849,Human_RBP_ID_18426775,Human_RBP_ID_23087924 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 65020 RMVar_ID_65020 Human_SNP_ID_386316845 m1A Human chr8 - 144517806 144517806 144517806 GCGGGAGATTCGCTGGACGATCGCAAGCGCGGAGGCCGGGCGGGCGCGCGCGCCATGGAGCGGCT GCGGGAGATTCGCTGGACGATCGCAAGCGCGGCGGCCGGGCGGGCGCGCGCGCCATGGAGCGGCT T G RECQL4 Ensembl:ENSG00000160957 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:144517723..144517809 26863410 MeRIP-seq:(Medium) rs1270450461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254976,Human_RBP_ID_4995834,Human_RBP_ID_9338849,Human_RBP_ID_18426775,Human_RBP_ID_23087924 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 65021 RMVar_ID_65021 Human_SNP_ID_386316957 m1A Human chr8 - 144518043 144518043 144518043 CCGCTCAGACACCCCCCCGGCCGCCCGCGCTCACCGGTCCCGCAACCGCAGCCACCGCCTCCAGC CCGCTCAGACACCCCCCCGGCCGCCCGCGCTCGCCGGTCCCGCAACCGCAGCCACCGCCTCCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144518017..144518224;chr8:144517976..144518462;chr8:144517976..144518413;chr8:144517926..144518450 26863196 MeRIP-seq:(Medium) rs1004216290 Functional Loss SNV dbSNP153 33..33 33 - - - 65022 RMVar_ID_65022 Human_SNP_ID_386317498 m1A Human chr8 - 144519798 144519798 144519798 GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCAAGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCATGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144519749..144519834 26863196 MeRIP-seq:(Medium) rs2721172 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 65023 RMVar_ID_65023 Human_SNP_ID_386317499 m1A Human chr8 - 144519798 144519798 144519798 GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCAAGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCAGGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144519749..144519834 26863196 MeRIP-seq:(Medium) rs2721172 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 65024 RMVar_ID_65024 Human_SNP_ID_386318924 m1A Human chr8 + 144522651 144522651 144522651 GCGCTCGTCGCGGAGCTCCTCTAGCTGTGCGAACGTACAGGGGCCGTCCAAGTAGTCGTTGACGA GCGCTCGTCGCGGAGCTCCTCTAGCTGTGCGACCGTACAGGGGCCGTCCAAGTAGTCGTTGACGA A C LRRC14 Ensembl:ENSG00000160959 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144522602..144522775 26863196 MeRIP-seq:(Medium) rs144936052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995836,Human_RBP_ID_27364415,Human_RBP_ID_27537004 65025 RMVar_ID_65025 Human_SNP_ID_386320604 m1A Human chr8 + 144526561 144526561 144526561 AAGCAGCCCAGAAATCCTTTTACCAGAGGACAACTCCCTAATCCGCTGGGCAGGGGCGGGGTGTC AAGCAGCCCAGAAATCCTTTTACCAGAGGACAGCTCCCTAATCCGCTGGGCAGGGGCGGGGTGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144524714..144527848 32194978 MeRIP-seq:(Medium) rs1034879512 Functional Loss SNV dbSNP153 33..33 33 - - - 65026 RMVar_ID_65026 Human_SNP_ID_386320629 m1A Human chr8 - 144526641 144526640 144526642 CGTTCCATCCTCTTCCCTCCCCGCTCCCGCACAGAGGGGCGCCCAGGAGGCAGTGACAGTCGTCG CGTTCCATCCTCTTCCCTCCCCGCTCCCGCA__GAGGGGCGCCCAGGAGGCAGTGACAGTCGTCG CTG C LRRC24,C8orf82 Ensembl:ENSG00000254402,Ensembl:ENSG00000213563 Protein coding,Protein coding intron,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144526568..144526667 26863410 MeRIP-seq:(Medium) rs777505239 Functional Loss DEL dbSNP153 32..33 33 - - - Human_miRNA_ID_325802,Human_miRNA_ID_577593,Human_miRNA_ID_2039796,Human_miRNA_ID_2077025,Human_miRNA_ID_3018777 RMVar_hsa_circ_255172,RMVar_hsa_circ_81459 65027 RMVar_ID_65027 Human_SNP_ID_386320660 m1A Human chr8 - 144526718 144526718 144526718 CGCAGCGCTGCAGAGGTGCGCAAGGGCCGCCCAAAGACCAGCTTGGGCCTCGCACTGCGCCCGAG CGCAGCGCTGCAGAGGTGCGCAAGGGCCGCCCGAAGACCAGCTTGGGCCTCGCACTGCGCCCGAG T C LRRC24,C8orf82 Ensembl:ENSG00000254402,Ensembl:ENSG00000213563 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144526672..144527012 26863196 MeRIP-seq:(Medium) rs1360528582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19022504 RMVar_hsa_circ_255172,RMVar_hsa_circ_81459 65028 RMVar_ID_65028 Human_SNP_ID_386320714 m1A Human chr8 - 144526842 144526842 144526842 GAGAAGGGCGTGGGTCCTGGAGGGGGATGGGGAACGCGGAGGCCACGCCCTCCCTGAGCCCGGCC GAGAAGGGCGTGGGTCCTGGAGGGGGATGGGGGACGCGGAGGCCACGCCCTCCCTGAGCCCGGCC T C LRRC24,C8orf82 Ensembl:ENSG00000254402,Ensembl:ENSG00000213563 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144526653..144526976 26863196 MeRIP-seq:(Medium) rs1008603087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268352,Human_RBP_ID_845093,Human_RBP_ID_959938,Human_RBP_ID_22732153 Human_miRNA_ID_2689675 RMVar_hsa_circ_255172,RMVar_hsa_circ_81459 65029 RMVar_ID_65029 Human_SNP_ID_386320832 m1A Human chr8 + 144527158 144527135 144527158 AGTCGGGTGCGCGGGGGGCGCGCGCCGTGGGGAGCGGGGTGTCCGGGAGGGCCGGGCCGCGGCAG AGTCGGGTGC_______________________GCGGGGTGTCCGGGAGGGCCGGGCCGCGGCAG CGCGGGGGGCGCGCGCCGTGGGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:144527109..144527454;chr8:144527109..144527327 26863196 MeRIP-seq:(Medium) rs1036588597 Functional Loss DEL dbSNP153 11..33 33 - - - 65030 RMVar_ID_65030 Human_SNP_ID_386320872 m1A Human chr8 + 144527231 144527231 144527231 ACAGCGCCGGGTGGGGGCGGGGCCGAGCGCGCAGGCGCACTAGGCTGCCGCGAGCGCGGGTGGCG ACAGCGCCGGGTGGGGGCGGGGCCGAGCGCGCGGGCGCACTAGGCTGCCGCGAGCGCGGGTGGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144526951..144527651 26863410 MeRIP-seq:(Medium) rs992052587 Functional Loss SNV dbSNP153 33..33 33 - - - 65031 RMVar_ID_65031 Human_SNP_ID_386320873 m1A Human chr8 + 144527231 144527231 144527231 ACAGCGCCGGGTGGGGGCGGGGCCGAGCGCGCAGGCGCACTAGGCTGCCGCGAGCGCGGGTGGCG ACAGCGCCGGGTGGGGGCGGGGCCGAGCGCGCTGGCGCACTAGGCTGCCGCGAGCGCGGGTGGCG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144526951..144527651 26863410 MeRIP-seq:(Medium) rs992052587 Functional Loss SNV dbSNP153 33..33 33 - - - 65032 RMVar_ID_65032 Human_SNP_ID_386321147 m1A Human chr8 - 144527740 144527740 144527740 TCACCTTCTTCTCCCGCCTGAGACCCAACCGCAGCGGGCGCTACGAGGCCGCTTTCCCCTTCCTC TCACCTTCTTCTCCCGCCTGAGACCCAACCGCTGCGGGCGCTACGAGGCCGCTTTCCCCTTCCTC T A C8orf82 Ensembl:ENSG00000213563 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144527601..144527749 26863196 MeRIP-seq:(Medium) rs151201677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845095,Human_RBP_ID_19022505 Human_Splice_Rec_1025152,Human_Splice_Rec_1025158,Human_Splice_Rec_1025164 RMVar_hsa_circ_255172,RMVar_hsa_circ_81459 65033 RMVar_ID_65033 Human_SNP_ID_386321162 m1A Human chr8 + 144527764 144527764 144527764 GCGCCCGCTGCGGTTGGGTCTCAGGCGGGAGAAGAAGGTGACCAGGAACTGCGGGTCTGGGGGAT GCGCCCGCTGCGGTTGGGTCTCAGGCGGGAGACGAAGGTGACCAGGAACTGCGGGTCTGGGGGAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144527534..144527799 26863196 MeRIP-seq:(Medium) rs1473052047 Functional Loss SNV dbSNP153 33..33 33 - - - 65034 RMVar_ID_65034 Human_SNP_ID_386321795 m1A Human chr8 + 144528781 144528778 144528781 GCCCCCGCCCACCTGGCCCTGGTGGTCCACGTAGTAGAAATACTCGCGGGTCCGCGGCTCCGGAC GCCCCCGCCCACCTGGCCCTGGTGGTCCAC___GTAGAAATACTCGCGGGTCCGCGGCTCCGGAC CGTA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144528043..144528984 32194978 MeRIP-seq:(Medium) rs1275519056 Functional Loss DEL dbSNP153 31..33 33 - - - 65035 RMVar_ID_65035 Human_SNP_ID_386321799 m1A Human chr8 + 144528781 144528781 144528781 GCCCCCGCCCACCTGGCCCTGGTGGTCCACGTAGTAGAAATACTCGCGGGTCCGCGGCTCCGGAC GCCCCCGCCCACCTGGCCCTGGTGGTCCACGTGGTAGAAATACTCGCGGGTCCGCGGCTCCGGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144528043..144528984 32194978 MeRIP-seq:(Medium) rs1236580432 Functional Loss SNV dbSNP153 33..33 33 - - - 65036 RMVar_ID_65036 Human_SNP_ID_386321892 m1A Human chr8 + 144528913 144528913 144528913 GGCCAGGGTCCGGAGCGTCCCGCAAGGCGGCCACATTCTCCTCCCGCGCCGGAAGCGACCAGCAG GGCCAGGGTCCGGAGCGTCCCGCAAGGCGGCCGCATTCTCCTCCCGCGCCGGAAGCGACCAGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:144528787..144529075;chr8:144528748..144529075 26863196 MeRIP-seq:(Medium) rs753686028 Functional Loss SNV dbSNP153 33..33 33 - - - 65037 RMVar_ID_65037 Human_SNP_ID_386322530 m1A Human chr8 - 144530406 144530406 144530406 TGGAGGGTGTGCTGTAGCGGGGGCGCCCGGGGACAGGAGGGATGTCCTGCCGCCCCCAGCCAGGC TGGAGGGTGTGCTGTAGCGGGGGCGCCCGGGGGCAGGAGGGATGTCCTGCCGCCCCCAGCCAGGC T C ARHGAP39 Ensembl:ENSG00000147799 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144530355..144530497 26863196 MeRIP-seq:(Medium) rs780491500 Functional Loss SNV dbSNP153 33..33 33 - - - 65038 RMVar_ID_65038 Human_SNP_ID_386328269 m1A Human chr8 + 144548200 144548200 144548200 ATAGCGCGGGGAGGAGGGCTGCGAGTCCCCGGAGGGCTTTCGGGGCTGGGCCAGCAGCGGGGAGC ATAGCGCGGGGAGGAGGGCTGCGAGTCCCCGGCGGGCTTTCGGGGCTGGGCCAGCAGCGGGGAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144548152..144548279 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 65039 RMVar_ID_65039 Human_SNP_ID_386328309 m1A Human chr8 + 144548286 144548284 144548287 TCTTCAGGAAGGGTGACGGCCTCCTCTCTGGGAAGAAGATGGTGCCGTCAGCCTCCGGGGCGAAG TCTTCAGGAAGGGTGACGGCCTCCTCTCTGG___GAAGATGGTGCCGTCAGCCTCCGGGGCGAAG GGAA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144548241..144548355 32194978 MeRIP-seq:(Medium) rs756238605 Functional Loss DEL dbSNP153 32..34 33 - - - 65040 RMVar_ID_65040 Human_SNP_ID_386339066 m1A Human chr8 - 144586422 144586422 144586422 GTGTCCTCGGCACACCCTGTGGGGCAGAGGAGAGAGGAGCCCGTCACCAAGGTGTAGCCCAGAGC GTGTCCTCGGCACACCCTGTGGGGCAGAGGAGGGAGGAGCCCGTCACCAAGGTGTAGCCCAGAGC T C ARHGAP39 Ensembl:ENSG00000147799 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144586409..144586489 26863196 MeRIP-seq:(Medium) rs1457021372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314579,RMVar_hsa_circ_292885 65041 RMVar_ID_65041 Human_SNP_ID_386346261 m1A Human chr8 - 144605689 144605655 144605690 GCACTGTTGCTTCTCCCCTCTTGCAGTGCGGCACCTTCCCGTCTGATGCTGGCGTTGTGCGTATG GCACTGTTGCTTCTCCCCTCTTGCAGTGCGG__________________________________ ACCATACGCACAACGCCAGCATCAGACGGGAAGGTG A ARHGAP39 Ensembl:ENSG00000147799 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144605665..144605735 26863196 MeRIP-seq:(Medium) rs759043152 Functional Loss DEL dbSNP153 32..65 33 - - - Human_miRNA_ID_449565,Human_miRNA_ID_453454,Human_miRNA_ID_585074,Human_miRNA_ID_1362923,Human_miRNA_ID_1424902 RMVar_hsa_circ_314579,RMVar_hsa_circ_292885,RMVar_hsa_circ_319560 65042 RMVar_ID_65042 Human_SNP_ID_386351792 m1A Human chr8 - 144624404 144624404 144624404 ATTGATCAGAGAGAAATGATGTGTTCTAGTTCATTCTCAGGCCCGGTGAGTTGTGGATTTCATGC ATTGATCAGAGAGAAATGATGTGTTCTAGTTCCTTCTCAGGCCCGGTGAGTTGTGGATTTCATGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:144624400..144624584 26863196 MeRIP-seq:(Medium) rs1033697653 Functional Loss SNV dbSNP153 33..33 33 - - - 65043 RMVar_ID_65043 Human_SNP_ID_386360998 m1A Human chr8 + 144662917 144662917 144662917 CATTATCCACCTCGGGCCTATCCCCCACCCCCATTATCCACCTTGGACTGCTCCCCACACCCCAT CATTATCCACCTCGGGCCTATCCCCCACCCCCCTTATCCACCTTGGACTGCTCCCCACACCCCAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144662915..144663022 26863196 MeRIP-seq:(Medium) rs1388243961 Functional Loss SNV dbSNP153 33..33 33 - - - 65044 RMVar_ID_65044 Human_SNP_ID_386361160 m1A Human chr8 - 144663537 144663537 144663537 TGGTTTGTTCAGTCCCGCCAGGTCTTGTGTTGAAGTTTAATCCCCAGTGTTGGAGGTGGGGCCTG TGGTTTGTTCAGTCCCGCCAGGTCTTGTGTTGGAGTTTAATCCCCAGTGTTGGAGGTGGGGCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144663535..144663713 26863196 MeRIP-seq:(Medium) rs1302602897 Functional Loss SNV dbSNP153 33..33 33 - - - 65045 RMVar_ID_65045 Human_SNP_ID_386362021 m1A Human chr8 + 144667172 144667172 144667172 AGACAAGGCAGATGCAGCACCCTGATGCTCCAAGCCCACCCGCACCCCCATTGCCTGTCCCCAGG AGACAAGGCAGATGCAGCACCCTGATGCTCCAGGCCCACCCGCACCCCCATTGCCTGTCCCCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144667169..144667384 26863196 MeRIP-seq:(Medium) rs1390897270 Functional Loss SNV dbSNP153 33..33 33 - - - 65046 RMVar_ID_65046 Human_SNP_ID_386363161 m1A Human chr8 - 144671640 144671640 144671640 GAGAAGGGGTGTCTTGTCTGGAAAGGAGGAGTATCAGCAGCTGAGCCTTGGGCTATTCACCAGGC GAGAAGGGGTGTCTTGTCTGGAAAGGAGGAGTGTCAGCAGCTGAGCCTTGGGCTATTCACCAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144671630..144671697 26863196 MeRIP-seq:(Medium) rs1213036309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16383606 65047 RMVar_ID_65047 Human_SNP_ID_386366833 m1A Human chr8 + 144684710 144684710 144684710 TCTCGCCGCCCTGGGCACGGAACGCCGCCTCCACCCACAGCACTCCAGCAACTGGGAAGCAACCG TCTCGCCGCCCTGGGCACGGAACGCCGCCTCCGCCCACAGCACTCCAGCAACTGGGAAGCAACCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144684700..144684966 32194978 MeRIP-seq:(Medium) rs1270299127 Functional Loss SNV dbSNP153 33..33 33 - - - 65048 RMVar_ID_65048 Human_SNP_ID_386367193 m1A Human chr8 - 144685806 144685792 144685806 GGCCGGCGGCGGCGGCGGAGGACGCCGACAGCACGGGCTGCCGCGGCAGCAGCGGCGGAGCAGCA GGCCGGCGGCGGCGGCGGAGGACGCCGACAGC______________CAGCAGCGGCGGAGCAGCA GCCGCGGCAGCCCGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144685012..144685875 26863196 MeRIP-seq:(Medium) rs1462282550 Functional Loss DEL dbSNP153 33..46 33 - - - 65049 RMVar_ID_65049 Human_SNP_ID_386370005 m1A Human chr8 + 144693993 144693993 144693993 TAGACAACAGAAGAGAGGGAAGGGCTGAGCCAAGCAAATAGCGAGGGCAAAGGAGAAAGGCAGTA TAGACAACAGAAGAGAGGGAAGGGCTGAGCCAGGCAAATAGCGAGGGCAAAGGAGAAAGGCAGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144693977..144694055 26863196 MeRIP-seq:(Medium) rs1256664113 Functional Loss SNV dbSNP153 33..33 33 - - - 65050 RMVar_ID_65050 Human_SNP_ID_386387163 m1A Human chr8 - 144755353 144755353 144755353 GGAAGGAGCGCCAAGCGGGCAGGCAGGCGGGGAGGGCGCGGGGAGGGCGCGGGGAGGCGGCGGCC GGAAGGAGCGCCAAGCGGGCAGGCAGGCGGGGGGGGCGCGGGGAGGGCGCGGGGAGGCGGCGGCC T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144755181..144755975 26863196 MeRIP-seq:(Medium) rs1050584455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090846,Human_RBP_ID_5224372,Human_RBP_ID_5406298,Human_RBP_ID_9440834,Human_RBP_ID_18426776,Human_RBP_ID_18467241,Human_RBP_ID_19022511,Human_RBP_ID_22419297,Human_RBP_ID_22732581,Human_RBP_ID_23088176,Human_RBP_ID_26795237 65051 RMVar_ID_65051 Human_SNP_ID_386387171 m1A Human chr8 - 144755361 144755361 144755361 TCGGACCAGGAAGGAGCGCCAAGCGGGCAGGCAGGCGGGGAGGGCGCGGGGAGGGCGCGGGGAGG TCGGACCAGGAAGGAGCGCCAAGCGGGCAGGCGGGCGGGGAGGGCGCGGGGAGGGCGCGGGGAGG T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144755312..144755507 26863196 MeRIP-seq:(Medium) rs1450519598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090846,Human_RBP_ID_5406298,Human_RBP_ID_9441577,Human_RBP_ID_18426776,Human_RBP_ID_18467241,Human_RBP_ID_22419297,Human_RBP_ID_23088176,Human_RBP_ID_26795237 65052 RMVar_ID_65052 Human_SNP_ID_386387183 m1A Human chr8 - 144755372 144755372 144755372 GTGGGGCAGTGTCGGACCAGGAAGGAGCGCCAAGCGGGCAGGCAGGCGGGGAGGGCGCGGGGAGG GTGGGGCAGTGTCGGACCAGGAAGGAGCGCCAGGCGGGCAGGCAGGCGGGGAGGGCGCGGGGAGG T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144755138..144755578 26863196 MeRIP-seq:(Medium) rs1303382420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090846,Human_RBP_ID_18426777,Human_RBP_ID_18467241,Human_RBP_ID_26795237 65053 RMVar_ID_65053 Human_SNP_ID_386396938 m1A Human chr8 + 144789825 144789825 144789825 GGCCCTCAGCACTAGTTCTCTTTCTCCTGCACAGTCTTGGTTCCCCGGAGACGTCCAGTCCGGCG GGCCCTCAGCACTAGTTCTCTTTCTCCTGCACGGTCTTGGTTCCCCGGAGACGTCCAGTCCGGCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:144789801..144789825 26863196 MeRIP-seq:(Medium) rs774382452 Functional Loss SNV dbSNP153 33..33 33 - - - 65054 RMVar_ID_65054 Human_SNP_ID_386396970 m1A Human chr8 - 144789942 144789942 144789942 CTCTGCCTGCAGCCTGTGGAGCATCCTTTTGGAGGTGGCAACCACCAGCACATCGGCAAGCCCTC CTCTGCCTGCAGCCTGTGGAGCATCCTTTTGGCGGTGGCAACCACCAGCACATCGGCAAGCCCTC T G RPL8 Ensembl:ENSG00000161016 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:144789842..144790002 26863410 MeRIP-seq:(Medium) rs1455438003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696096,Human_RBP_ID_2053538,Human_RBP_ID_3874918,Human_RBP_ID_8683392,Human_RBP_ID_18125157,Human_RBP_ID_18196683,Human_RBP_ID_22465064,Human_RBP_ID_22534452,Human_RBP_ID_26833107 Human_Splice_Rec_1025278,Human_Splice_Rec_1025286,Human_Splice_Rec_1025292,Human_Splice_Rec_1025298,Human_Splice_Rec_1025306,Human_Splice_Rec_1025316,Human_Splice_Rec_1025324,Human_Splice_Rec_1025334,Human_Splice_Rec_1025342,Human_Splice_Rec_1025352,Human_Splice_Rec_1025362 Human_miRNA_ID_209271,Human_miRNA_ID_2015782,Human_miRNA_ID_2015783,Human_miRNA_ID_2051419,Human_miRNA_ID_2051420 RMVar_hsa_circ_82581,RMVar_hsa_circ_119399,RMVar_hsa_circ_99078,RMVar_hsa_circ_116594,RMVar_hsa_circ_82967,RMVar_hsa_circ_255180,RMVar_hsa_circ_77055,RMVar_hsa_circ_80417,RMVar_hsa_circ_255182,RMVar_hsa_circ_255184,RMVar_hsa_circ_255185,RMVar_hsa_circ_255183,RMVar_hsa_circ_255181,RMVar_hsa_circ_255179 65055 RMVar_ID_65055 Human_SNP_ID_386397187 m1A Human chr8 + 144790424 144790424 144790424 CTCTTTGCCTTATATTTGTGGTACGCCCGGCCAGCCTTCAAGATGGGTTTGTCAATTCGGCCACC CTCTTTGCCTTATATTTGTGGTACGCCCGGCCCGCCTTCAAGATGGGTTTGTCAATTCGGCCACC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144790401..144790425 26863196 MeRIP-seq:(Medium) rs754924690 Functional Loss SNV dbSNP153 33..33 33 - - - 65056 RMVar_ID_65056 Human_SNP_ID_386397188 m1A Human chr8 + 144790424 144790424 144790424 CTCTTTGCCTTATATTTGTGGTACGCCCGGCCAGCCTTCAAGATGGGTTTGTCAATTCGGCCACC CTCTTTGCCTTATATTTGTGGTACGCCCGGCCGGCCTTCAAGATGGGTTTGTCAATTCGGCCACC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:144790401..144790425 26863196 MeRIP-seq:(Medium) rs754924690 Functional Loss SNV dbSNP153 33..33 33 - - - 65057 RMVar_ID_65057 Human_SNP_ID_386397199 m1A Human chr8 + 144790454 144790454 144790454 CCAGCCTTCAAGATGGGTTTGTCAATTCGGCCACCTCCAGCCACCACACCTGTAGGGGATCAGAT CCAGCCTTCAAGATGGGTTTGTCAATTCGGCCCCCTCCAGCCACCACACCTGTAGGGGATCAGAT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr8:144790289..144790534;chr8:144790325..144790505 26863196,26863410 MeRIP-seq:(Medium) rs776854981 Functional Loss SNV dbSNP153 33..33 33 - - - 65058 RMVar_ID_65058 Human_SNP_ID_386397800 m1A Human chr8 - 144791844 144791844 144791844 CAAGGTGGTCTTCCGGGATCCGTATCGGTTTAAGAAGCGGACGGAGCTGTTCATTGCCGCCGAGG CAAGGTGGTCTTCCGGGATCCGTATCGGTTTAGGAAGCGGACGGAGCTGTTCATTGCCGCCGAGG T C RPL8 Ensembl:ENSG00000161016 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:144791807..144791893 26863410 MeRIP-seq:(Medium) rs753348792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88833,Human_RBP_ID_696115,Human_RBP_ID_1054741,Human_RBP_ID_1400834,Human_RBP_ID_1694340,Human_RBP_ID_2053545,Human_RBP_ID_4975995,Human_RBP_ID_8683404,Human_RBP_ID_9222162,Human_RBP_ID_16384834,Human_RBP_ID_17666061,Human_RBP_ID_17714320,Human_RBP_ID_18114300,Human_RBP_ID_18196694,Human_RBP_ID_18893960,Human_RBP_ID_22465066,Human_RBP_ID_24250420,Human_RBP_ID_24519736,Human_RBP_ID_26833122,Human_RBP_ID_27123192 Human_Splice_Rec_1025280,Human_Splice_Rec_1025281,Human_Splice_Rec_1025293,Human_Splice_Rec_1025300,Human_Splice_Rec_1025310,Human_Splice_Rec_1025311,Human_Splice_Rec_1025328,Human_Splice_Rec_1025329,Human_Splice_Rec_1025336,Human_Splice_Rec_1025337,Human_Splice_Rec_1025344,Human_Splice_Rec_1025345,Human_Splice_Rec_1025354,Human_Splice_Rec_1025355,Human_Splice_Rec_1025366,Human_Splice_Rec_1025367,Human_Splice_Rec_1025374,Human_Splice_Rec_1025378 RMVar_hsa_circ_82581,RMVar_hsa_circ_119399,RMVar_hsa_circ_255180,RMVar_hsa_circ_77055,RMVar_hsa_circ_80417,RMVar_hsa_circ_255182,RMVar_hsa_circ_255181,RMVar_hsa_circ_255179,RMVar_hsa_circ_97186,RMVar_hsa_circ_255188,RMVar_hsa_circ_255190,RMVar_hsa_circ_95117,RMVar_hsa_circ_301737,RMVar_hsa_circ_255189 65059 RMVar_ID_65059 Human_SNP_ID_386397945 m1A Human chr8 - 144792101 144792101 144792101 CGCCATGGGCCGTGTGATCCGTGGACAGAGGAAGGGCGCCGGGTCTGTGTTCCGCGCGCACGTGA CGCCATGGGCCGTGTGATCCGTGGACAGAGGAGGGGCGCCGGGTCTGTGTTCCGCGCGCACGTGA T C RPL8 Ensembl:ENSG00000161016 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:144791998..144792122 26863410 MeRIP-seq:(Medium) rs1234028238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88834,Human_RBP_ID_254987,Human_RBP_ID_271028,Human_RBP_ID_696121,Human_RBP_ID_795846,Human_RBP_ID_845087,Human_RBP_ID_959925,Human_RBP_ID_1694349,Human_RBP_ID_2053550,Human_RBP_ID_4976001,Human_RBP_ID_5223305,Human_RBP_ID_7818507,Human_RBP_ID_8273983,Human_RBP_ID_8683411,Human_RBP_ID_9222165,Human_RBP_ID_9338562,Human_RBP_ID_16384844,Human_RBP_ID_17665577,Human_RBP_ID_17714324,Human_RBP_ID_18114309,Human_RBP_ID_18196699,Human_RBP_ID_18893967,Human_RBP_ID_21599083,Human_RBP_ID_22465751,Human_RBP_ID_23140708,Human_RBP_ID_24250422 Human_Splice_Rec_1025308,Human_Splice_Rec_1025318,Human_Splice_Rec_1025326,Human_Splice_Rec_1025364,Human_Splice_Rec_1025372,Human_Splice_Rec_1025376 Human_miRNA_ID_1967756,Human_miRNA_ID_1967757,Human_miRNA_ID_3115063,Human_miRNA_ID_3115064 RMVar_hsa_circ_82581,RMVar_hsa_circ_255180,RMVar_hsa_circ_77055,RMVar_hsa_circ_80417,RMVar_hsa_circ_255181,RMVar_hsa_circ_255179,RMVar_hsa_circ_97186,RMVar_hsa_circ_255188,RMVar_hsa_circ_255190,RMVar_hsa_circ_301737,RMVar_hsa_circ_284634 65060 RMVar_ID_65060 Human_SNP_ID_386400079 m1A Human chr8 + 144798935 144798935 144798935 GTGCGCTCCTCCCCGCGCTGTCTCGGCGGCCCAGGGTGAGTCGGCCGCGGCCGCGGGGCGGGGAC GTGCGCTCCTCCCCGCGCTGTCTCGGCGGCCCGGGGTGAGTCGGCCGCGGCCGCGGGGCGGGGAC A G ZNF517 Ensembl:ENSG00000197363 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144798931..144799208 26863196 MeRIP-seq:(Medium) rs984971400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5480856,Human_RBP_ID_7818513,Human_RBP_ID_27537065 Human_Splice_Rec_1025379,Human_Splice_Rec_1025387,Human_Splice_Rec_1025397,Human_Splice_Rec_1025405,Human_Splice_Rec_1025409 65061 RMVar_ID_65061 Human_SNP_ID_386403446 m1A Human chr8 - 144808994 144808990 144808995 CTACAGCGTACAGGCACAGACCACGATACCTGACTTATTTTTAAATTTTTTGTAGAGAAGTTTCA CTACAGCGTACAGGCACAGACCACGATACCT_____ATTTTTAAATTTTTTGTAGAGAAGTTTCA TAAGTC T LOC100130027-001 RNACentral:URS0000BC447A lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1170258354 Functional Loss DEL dbSNP153 32..36 33 - - - 65062 RMVar_ID_65062 Human_SNP_ID_386403447 m1A Human chr8 - 144808994 144808994 144808994 CTACAGCGTACAGGCACAGACCACGATACCTGACTTATTTTTAAATTTTTTGTAGAGAAGTTTCA CTACAGCGTACAGGCACAGACCACGATACCTGGCTTATTTTTAAATTTTTTGTAGAGAAGTTTCA T C LOC100130027-001 RNACentral:URS0000BC447A lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2954668 Functional Loss SNV dbSNP153 33..33 33 - - - 65063 RMVar_ID_65063 Human_SNP_ID_386405862 m1A Human chr8 - 144817470 144817470 144817470 TAGTGGAGAGGTAGAAGGAAAACCCAGAGTGCAGTGTCATGAAAATACAGGGAAGGGACGATTGA TAGTGGAGAGGTAGAAGGAAAACCCAGAGTGCGGTGTCATGAAAATACAGGGAAGGGACGATTGA T C LOC100130027-001 RNACentral:URS0000BC447A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144817424..144817515 26863196 MeRIP-seq:(Medium) rs1444524918 Functional Loss SNV dbSNP153 33..33 33 - - - 65064 RMVar_ID_65064 Human_SNP_ID_386409171 m1A Human chr8 - 144829536 144829535 144829537 CTTCCCTGTAGAGGGCCCTCTGGCCAGGGTCCAGACACTGCCACTCCTCCCGAGAGAAGTGCACA CTTCCCTGTAGAGGGCCCTCTGGCCAGGGTC__GACACTGCCACTCCTCCCGAGAGAAGTGCACA CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144829441..144829555 26863196 MeRIP-seq:(Medium) rs1293089992 Functional Loss DEL dbSNP153 32..33 33 - - - 65065 RMVar_ID_65065 Human_SNP_ID_386416052 m1A Human chr8 - 144851348 144851348 144851348 ACCGACCTCCTGGGCTGGCTGATCAAAGAGGAAGCAGCAGCAATGTCTGCTGTGGGGGCTGCAAC ACCGACCTCCTGGGCTGGCTGATCAAAGAGGAGGCAGCAGCAATGTCTGCTGTGGGGGCTGCAAC T C COMMD5 Ensembl:ENSG00000170619 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144851297..144852380 26863196 MeRIP-seq:(Medium) rs1180182954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995852 Human_Splice_Rec_1025558,Human_Splice_Rec_1025560,Human_Splice_Rec_1025562,Human_Splice_Rec_1025564,Human_Splice_Rec_1025566,Human_Splice_Rec_1025568 65066 RMVar_ID_65066 Human_SNP_ID_386416431 m1A Human chr8 + 144852785 144852784 144852786 GCCCGTTCCGGGGCGCGGGGACCTTGGTGCACAGAGTCAAATTGGCACTCGGCCGTCGCCGCCCC GCCCGTTCCGGGGCGCGGGGACCTTGGTGCAC__AGTCAAATTGGCACTCGGCCGTCGCCGCCCC CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144852782..144853050 26863196 MeRIP-seq:(Medium) rs1312969359 Functional Loss DEL dbSNP153 33..34 33 - - - 65067 RMVar_ID_65067 Human_SNP_ID_386416432 m1A Human chr8 + 144852785 144852785 144852785 GCCCGTTCCGGGGCGCGGGGACCTTGGTGCACAGAGTCAAATTGGCACTCGGCCGTCGCCGCCCC GCCCGTTCCGGGGCGCGGGGACCTTGGTGCACGGAGTCAAATTGGCACTCGGCCGTCGCCGCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144852782..144853050 26863196 MeRIP-seq:(Medium) rs975050548 Functional Loss SNV dbSNP153 33..33 33 - - - 65068 RMVar_ID_65068 Human_SNP_ID_386416452 m1A Human chr8 - 144852849 144852849 144852849 GCTCTGGATACTGCGGGGCTTTTCCGCGGAGGAGCGCCCGCCGGTAGGTTGGCCCCGAACCGTGG GCTCTGGATACTGCGGGGCTTTTCCGCGGAGGGGCGCCCGCCGGTAGGTTGGCCCCGAACCGTGG T C COMMD5 Ensembl:ENSG00000170619 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr8:144852841..144853018;chr8:144852841..144853038;chr8:144852841..144852940 26863196,32194978 MeRIP-seq:(Medium) rs1469221015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996499,Human_RBP_ID_5123584,Human_RBP_ID_19142185 Human_Splice_Rec_1025561 65069 RMVar_ID_65069 Human_SNP_ID_386423282 m1A Human chr8 + 144881705 144881705 144881705 ACTCATATGGCTTCTCGCCCGTGTGGGTCCTCAGGTGCACAATCAGAGTTGCTTTCAGGCTGAAG ACTCATATGGCTTCTCGCCCGTGTGGGTCCTCGGGTGCACAATCAGAGTTGCTTTCAGGCTGAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:144881656..144881756 32194978 MeRIP-seq:(Medium) rs763558755 Functional Loss SNV dbSNP153 33..33 33 - - - 65070 RMVar_ID_65070 Human_SNP_ID_386423458 m1A Human chr8 - 144882303 144882303 144882303 GTCGGAAAGCCTTCACTCAACTCTCACATCTCATTCAGCACCAGCGGATCCACACGGGAGAAAGG GTCGGAAAGCCTTCACTCAACTCTCACATCTCTTTCAGCACCAGCGGATCCACACGGGAGAAAGG T A ZNF250 Ensembl:ENSG00000196150 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:144882252..144882402 32194978 MeRIP-seq:(Medium) rs1348002810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18114349 Human_miRNA_ID_2051422 RMVar_hsa_circ_77403,RMVar_hsa_circ_114347,RMVar_hsa_circ_255199,RMVar_hsa_circ_255200,RMVar_hsa_circ_67182,RMVar_hsa_circ_255201,RMVar_hsa_circ_306556,RMVar_hsa_circ_255202,RMVar_hsa_circ_255203 65071 RMVar_ID_65071 Human_SNP_ID_386426422 m1A Human chr8 - 144894134 144894134 144894134 GAAGAAGGAAGGAGGCTGATGCACAGGCTCACAGACCAAGCTGGGGGTAGAAATGATGGTAGAGG GAAGAAGGAAGGAGGCTGATGCACAGGCTCACGGACCAAGCTGGGGGTAGAAATGATGGTAGAGG T C ZNF250 Ensembl:ENSG00000196150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144894128..144894220 26863196 MeRIP-seq:(Medium) rs1180080990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24250514 RMVar_hsa_circ_77403,RMVar_hsa_circ_51234,RMVar_hsa_circ_255200,RMVar_hsa_circ_255201 65072 RMVar_ID_65072 Human_SNP_ID_386428071 m1A Human chr8 - 144901319 144901319 144901319 CGGACACCGGAGCCGGTGCGTCCTCCACACGAATCGTGGACTCTTCCCCGCGAGCACGCACTGCC CGGACACCGGAGCCGGTGCGTCCTCCACACGAGTCGTGGACTCTTCCCCGCGAGCACGCACTGCC T C ZNF250 Ensembl:ENSG00000196150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144901304..144901387 26863196 MeRIP-seq:(Medium) rs1388529095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77403,RMVar_hsa_circ_255200,RMVar_hsa_circ_255201 65073 RMVar_ID_65073 Human_SNP_ID_386436775 m1A Human chr8 - 144933795 144933795 144933795 CCAGCAAGGCCTGTGCAAGGGAAGTGGGTAGCACGAGGGCCATGTGGAGAGTGCTCTGGGCAAGG CCAGCAAGGCCTGTGCAAGGGAAGTGGGTAGCTCGAGGGCCATGTGGAGAGTGCTCTGGGCAAGG T A ZNF16 Ensembl:ENSG00000170631 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144933788..144933901 26863196 MeRIP-seq:(Medium) rs1388866927 Functional Loss SNV dbSNP153 33..33 33 - - - 65074 RMVar_ID_65074 Human_SNP_ID_386456059 m1A Human chr8 - 145002510 145002510 145002510 AAGCCAGATGGGTAAAAAGATCTCGCAGAGGAAGGGAGTTTGGGCAATGTCAGGGGATGAGCTGA AAGCCAGATGGGTAAAAAGATCTCGCAGAGGACGGGAGTTTGGGCAATGTCAGGGGATGAGCTGA T G ZNF252P Ensembl:ENSG00000196922 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:145002489..145002845 26863196 MeRIP-seq:(Medium) rs1340167831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255210,RMVar_hsa_circ_86813 65075 RMVar_ID_65075 Human_SNP_ID_386456352 m1A Human chr8 + 145003166 145003166 145003166 TCCTCAACCGGGGGTTGTTCTCCGTGCTCTGGACCCGGCCCTTCCTCACCTAGGACGTCTCGCGG TCCTCAACCGGGGGTTGTTCTCCGTGCTCTGGGCCCGGCCCTTCCTCACCTAGGACGTCTCGCGG A G ZNF252P-AS1 Ensembl:ENSG00000255559 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:145003109..145003209 26863196 MeRIP-seq:(Medium) rs117777718 Functional Loss SNV dbSNP153 33..33 33 - - - 65076 RMVar_ID_65076 Human_SNP_ID_386469560 m1A Human chr8 - 145052540 145052540 145052540 GGTAGCACGAGGGTCACCGAGAGCCGCCAACAATGCAAGGCCCAGCCACCCGCGCGTCTTCTCCA GGTAGCACGAGGGTCACCGAGAGCCGCCAACATTGCAAGGCCCAGCCACCCGCGCGTCTTCTCCA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:145052476..145052700 26863196 MeRIP-seq:(Medium) rs1487251371 Functional Loss SNV dbSNP153 33..33 33 - - - 65077 RMVar_ID_65077 Human_SNP_ID_386469561 m1A Human chr8 - 145052540 145052540 145052540 GGTAGCACGAGGGTCACCGAGAGCCGCCAACAATGCAAGGCCCAGCCACCCGCGCGTCTTCTCCA GGTAGCACGAGGGTCACCGAGAGCCGCCAACAGTGCAAGGCCCAGCCACCCGCGCGTCTTCTCCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:145052476..145052700 26863196 MeRIP-seq:(Medium) rs1487251371 Functional Loss SNV dbSNP153 33..33 33 - - - 65078 RMVar_ID_65078 Human_SNP_ID_386469688 m1A Human chr8 + 145052714 145052714 145052714 GCCCGGAATCCTTCCACTGTCTGTCTCTGCCCAGAGCAACCTACGTGCAGTAACGCTGACTCCAG GCCCGGAATCCTTCCACTGTCTGTCTCTGCCCCGAGCAACCTACGTGCAGTAACGCTGACTCCAG A C C8orf33 Ensembl:ENSG00000182307 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:145052576..145052775 32194978 MeRIP-seq:(Medium) rs1356015212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696217,Human_RBP_ID_1224056,Human_RBP_ID_1694377,Human_RBP_ID_4976189,Human_RBP_ID_8683502,Human_RBP_ID_9313757,Human_RBP_ID_16385528,Human_RBP_ID_18114397,Human_RBP_ID_22330418,Human_RBP_ID_22465754 Human_miRNA_ID_2424136,Human_miRNA_ID_2433796,Human_miRNA_ID_2907327,Human_miRNA_ID_3026163 RMVar_hsa_circ_102981,RMVar_hsa_circ_107432,RMVar_hsa_circ_255212,RMVar_hsa_circ_255213 65079 RMVar_ID_65079 Human_SNP_ID_386469689 m1A Human chr8 + 145052714 145052714 145052714 GCCCGGAATCCTTCCACTGTCTGTCTCTGCCCAGAGCAACCTACGTGCAGTAACGCTGACTCCAG GCCCGGAATCCTTCCACTGTCTGTCTCTGCCCGGAGCAACCTACGTGCAGTAACGCTGACTCCAG A G C8orf33 Ensembl:ENSG00000182307 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:145052576..145052775 32194978 MeRIP-seq:(Medium) rs1356015212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696217,Human_RBP_ID_1224056,Human_RBP_ID_1694377,Human_RBP_ID_4976189,Human_RBP_ID_8683502,Human_RBP_ID_9313757,Human_RBP_ID_16385528,Human_RBP_ID_18114397,Human_RBP_ID_22330418,Human_RBP_ID_22465754 Human_miRNA_ID_2424136,Human_miRNA_ID_2433796,Human_miRNA_ID_2907327,Human_miRNA_ID_3026163 RMVar_hsa_circ_102981,RMVar_hsa_circ_107432,RMVar_hsa_circ_255212,RMVar_hsa_circ_255213 65080 RMVar_ID_65080 Human_SNP_ID_386470777 m1A Human chr8 + 145055781 145055781 145055781 ATTAGTGAAAGTACTAAATGTCTGATATGCAGAAATAATGGCATAAGCTGTCTCTCTCTCTTCTC ATTAGTGAAAGTACTAAATGTCTGATATGCAGCAATAATGGCATAAGCTGTCTCTCTCTCTTCTC A C C8orf33 Ensembl:ENSG00000182307 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:145055730..145055810 26863196 MeRIP-seq:(Medium) rs1317044621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696276,Human_RBP_ID_18388251,Human_RBP_ID_24250655 Human_miRNA_ID_2205187,Human_miRNA_ID_2928921 RMVar_hsa_circ_102981,RMVar_hsa_circ_116811,RMVar_hsa_circ_107432,RMVar_hsa_circ_255212,RMVar_hsa_circ_255213,RMVar_hsa_circ_109900,RMVar_hsa_circ_255214,RMVar_hsa_circ_255215 65081 RMVar_ID_65081 Human_SNP_ID_337754423 m1A Human chr7 - 120857938 120857938 120857938 GCGGGGGGAGAGGAAGAGAAAGAAGCGTCTCCAGCTGAAGCCAATGCAGCCCTCCGGCTCTCCGC GCGGGGGGAGAGGAAGAGAAAGAAGCGTCTCCCGCTGAAGCCAATGCAGCCCTCCGGCTCTCCGC T G TSPAN12 Ensembl:ENSG00000106025 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:120857784..120858086;chr7:120857341..120858105;chr7:120857801..120858105 26863196 MeRIP-seq:(Medium) rs1248584000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4922417,Human_RBP_ID_24186714 Human_Splice_Rec_915464,Human_Splice_Rec_915506 Human_miRNA_ID_2445315,Human_miRNA_ID_2446700 RMVar_hsa_circ_109008,RMVar_hsa_circ_352566,RMVar_hsa_circ_358007,RMVar_hsa_circ_248012,RMVar_hsa_circ_358664 65082 RMVar_ID_65082 Human_SNP_ID_337775761 m1A Human chr7 - 120950884 120950884 120950884 TAGTCTTCTAGGTACAACATCGCGGCCCTTAGAGCTGAGGGAACAAGGGGGTCCAGGGGTTTATT TAGTCTTCTAGGTACAACATCGCGGCCCTTAGTGCTGAGGGAACAAGGGGGTCCAGGGGTTTATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:120950834..120950955 26863196 MeRIP-seq:(Medium) rs1296294970 Functional Loss SNV dbSNP153 33..33 33 - - - 65083 RMVar_ID_65083 Human_SNP_ID_337778239 m1A Human chr7 - 120960296 120960296 120960296 ACTCTCCTCCTAGACTGGCTCGCAAGGCCCCCATGCATTAGCTCCTGCCTGCTTCCTTTCATGCT ACTCTCCTCCTAGACTGGCTCGCAAGGCCCCCGTGCATTAGCTCCTGCCTGCTTCCTTTCATGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:120960151..120960338 26863196 MeRIP-seq:(Medium) rs184574679 Functional Loss SNV dbSNP153 33..33 33 - - - 65084 RMVar_ID_65084 Human_SNP_ID_337778240 m1A Human chr7 - 120960296 120960296 120960296 ACTCTCCTCCTAGACTGGCTCGCAAGGCCCCCATGCATTAGCTCCTGCCTGCTTCCTTTCATGCT ACTCTCCTCCTAGACTGGCTCGCAAGGCCCCCCTGCATTAGCTCCTGCCTGCTTCCTTTCATGCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:120960151..120960338 26863196 MeRIP-seq:(Medium) rs184574679 Functional Loss SNV dbSNP153 33..33 33 - - - 65085 RMVar_ID_65085 Human_SNP_ID_338444946 m1A Human chr7 - 123692650 123692650 123692650 CCGCCAAATAGGATGTACCCTCCTCCACCTCCAGCCCTTCCCTCCTCAGCACCTTCAGGGCCTCC CCGCCAAATAGGATGTACCCTCCTCCACCTCCTGCCCTTCCCTCCTCAGCACCTTCAGGGCCTCC T A WASL Ensembl:ENSG00000106299 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:123692518..123692754 26863196 MeRIP-seq:(Medium) rs745885148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18960364,Human_RBP_ID_27830760 Human_miRNA_ID_848020,Human_miRNA_ID_1386732 RMVar_hsa_circ_39833,RMVar_hsa_circ_248130,RMVar_hsa_circ_286138,RMVar_hsa_circ_346872,RMVar_hsa_circ_57190,RMVar_hsa_circ_71122 65086 RMVar_ID_65086 Human_SNP_ID_338444953 m1A Human chr7 + 123692667 123692667 123692667 TGAGGAGGGAAGGGCTGGAGGTGGAGGAGGGTACATCCTATTTGGCGGTGGTGGAGGGACTGCTA TGAGGAGGGAAGGGCTGGAGGTGGAGGAGGGTGCATCCTATTTGGCGGTGGTGGAGGGACTGCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:123692560..123692771;chr7:123692548..123692725 26863196 MeRIP-seq:(Medium) rs1168900267 Functional Loss SNV dbSNP153 33..33 33 - - - 65087 RMVar_ID_65087 Human_SNP_ID_338703715 m1A Human chr7 - 124765691 124765667 124765692 ACGATTTCCTTCTCTGCGGCGGCACGCCGTCCAGCAGCCTGCTTCGCCCCGTCGTCAACTTTGAG ACGATTTCCTTCTCTGCGGCGGCACGCCGTC_________________________AACTTTGAG TGACGACGGGGCGAAGCAGGCTGCTG T GPR37 Ensembl:ENSG00000170775 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:124765642..124765770 26863196 MeRIP-seq:(Medium) rs1333496953 Functional Loss DEL dbSNP153 32..56 33 - - - 65088 RMVar_ID_65088 Human_SNP_ID_339316220 m1A Human chr7 + 127295642 127295642 127295642 TGCCGGCACCGTGAAGATCTGGACTTCAGAGCATGTCTTTGACCACTCATGGGAAACTGTTACAA TGCCGGCACCGTGAAGATCTGGACTTCAGAGCGTGTCTTTGACCACTCATGGGAAACTGTTACAA A G PRELID3BP10 Ensembl:ENSG00000236105 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:127295615..127295700 26863410 MeRIP-seq:(Medium) rs866573440 Functional Loss SNV dbSNP153 33..33 33 - - - 65089 RMVar_ID_65089 Human_SNP_ID_339338878 m1A Human chr7 - 127392159 127392159 127392159 GGTTCCCCCGCGTGGTCAGCGGAGGCTGCGCCAGGTGGGGCCCGCAGCCGCCTCCCACGCCAGGC GGTTCCCCCGCGTGGTCAGCGGAGGCTGCGCCGGGTGGGGCCCGCAGCCGCCTCCCACGCCAGGC T C ZNF800 Ensembl:ENSG00000048405 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:127392111..127392226 26863196 MeRIP-seq:(Medium) rs1316352293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4923097 Human_Splice_Rec_919401,Human_Splice_Rec_919411,Human_Splice_Rec_919431,Human_Splice_Rec_919447 65090 RMVar_ID_65090 Human_SNP_ID_339383234 m1A Human chr7 - 127582264 127582264 127582264 TCAGCTGCAGGATCGGCTGCTGGAGGAGGGCGAACGGCATCGTGAGGAGGTTGCAGCCCTGCAGA TCAGCTGCAGGATCGGCTGCTGGAGGAGGGCGGACGGCATCGTGAGGAGGTTGCAGCCCTGCAGA T C GCC1 Ensembl:ENSG00000179562 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr7:127582214..127582302;chr7:127582213..127582612 26863196,32194978 MeRIP-seq:(Medium) rs73234845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18091466 RMVar_hsa_circ_80517,RMVar_hsa_circ_248174 65091 RMVar_ID_65091 Human_SNP_ID_339384373 m1A Human chr7 - 127585530 127585530 127585530 ATGGGACCGAGCTCAGCGTAACCCTCTGGCCGACGTGGGCCGAGGGGGCCGGCCCGGGCTGCTGT ATGGGACCGAGCTCAGCGTAACCCTCTGGCCGGCGTGGGCCGAGGGGGCCGGCCCGGGCTGCTGT T C GCC1 Ensembl:ENSG00000179562 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:127585480..127585565 26863196 MeRIP-seq:(Medium) rs753728738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4923220,Human_RBP_ID_8915078,Human_RBP_ID_9311449,Human_RBP_ID_18091479,Human_RBP_ID_24187964,Human_RBP_ID_26357043 RMVar_hsa_circ_80517,RMVar_hsa_circ_248174 65092 RMVar_ID_65092 Human_SNP_ID_339385181 m1A Human chr7 - 127588484 127588473 127588485 GGACACGGTGAGGCCCATGGCGGGGCCCGGGGAGGGGCGCGGGCACCGACGCGGGGTGCGGGCTG GGACACGGTGAGGCCCATGGCGGGGCCCGGG____________CACCGACGCGGGGTGCGGGCTG GCCCGCGCCCCTC G GCC1 Ensembl:ENSG00000179562 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:127588376..127588600 26863410 MeRIP-seq:(Medium) rs780563957 Functional Loss DEL dbSNP153 32..43 33 - - - 65093 RMVar_ID_65093 Human_SNP_ID_339385188 m1A Human chr7 - 127588484 127588480 127588484 GGACACGGTGAGGCCCATGGCGGGGCCCGGGGAGGGGCGCGGGCACCGACGCGGGGTGCGGGCTG GGACACGGTGAGGCCCATGGCGGGGCCCGGGG____GCGCGGGCACCGACGCGGGGTGCGGGCTG CCCCT C GCC1 Ensembl:ENSG00000179562 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:127588376..127588600 26863410 MeRIP-seq:(Medium) rs756556208 Functional Loss DEL dbSNP153 33..36 33 - - - 65094 RMVar_ID_65094 Human_SNP_ID_339386045 m1A Human chr7 + 127591248 127591248 127591248 TATGTCCAGGCCACCTGTGCCACCCAAGGCACAGGTCTGTACGATGGTCTGGACTGGCTGTCCCA TATGTCCAGGCCACCTGTGCCACCCAAGGCACCGGTCTGTACGATGGTCTGGACTGGCTGTCCCA A C ARF5 Ensembl:ENSG00000004059 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:127590951..127591656 32194978 MeRIP-seq:(Medium) rs77229708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1681266,Human_RBP_ID_4959607,Human_RBP_ID_5219238,Human_RBP_ID_5451827 Human_Splice_Rec_919484,Human_Splice_Rec_919506 65095 RMVar_ID_65095 Human_SNP_ID_339386046 m1A Human chr7 + 127591248 127591248 127591248 TATGTCCAGGCCACCTGTGCCACCCAAGGCACAGGTCTGTACGATGGTCTGGACTGGCTGTCCCA TATGTCCAGGCCACCTGTGCCACCCAAGGCACGGGTCTGTACGATGGTCTGGACTGGCTGTCCCA A G ARF5 Ensembl:ENSG00000004059 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:127590951..127591656 32194978 MeRIP-seq:(Medium) rs77229708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1681266,Human_RBP_ID_4959607,Human_RBP_ID_5219238,Human_RBP_ID_5451827 Human_Splice_Rec_919484,Human_Splice_Rec_919506 65096 RMVar_ID_65096 Human_SNP_ID_339402135 m1A Human chr7 - 127652283 127652283 127652283 GGTGTCGGTGTTGGTGAAAGGGAGTCGAGGCGAGGGGCAGGCTGGCTACCAGCTGCGGACGGTGG GGTGTCGGTGTTGGTGAAAGGGAGTCGAGGCGGGGGGCAGGCTGGCTACCAGCTGCGGACGGTGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:127652176..127652420 26863196 MeRIP-seq:(Medium) rs1479955630 Functional Loss SNV dbSNP153 33..33 33 - - - 65097 RMVar_ID_65097 Human_SNP_ID_339414658 m1A Human chr7 - 127707509 127707509 127707509 GGATGCAAGATCATTCAGACTCAGCAAATGGAATCCACCACTACCATGGGAGCACAGTTGGTGCA GGATGCAAGATCATTCAGACTCAGCAAATGGAGTCCACCACTACCATGGGAGCACAGTTGGTGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:127707505..127707695 26863196 MeRIP-seq:(Medium) rs769563341 Functional Loss SNV dbSNP153 33..33 33 - - - 65098 RMVar_ID_65098 Human_SNP_ID_339437011 m1A Human chr7 + 127807526 127807526 127807526 AGAAACTGCGTCCCCTGTATGACATTCCTTACATGTTTGAGGCCCGGGAATTTCTTCGAAAAAAG AGAAACTGCGTCCCCTGTATGACATTCCTTACGTGTTTGAGGCCCGGGAATTTCTTCGAAAAAAG A G SND1 Ensembl:ENSG00000197157 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:127721392..127888003 32194978 MeRIP-seq:(Medium) rs189206929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_315464,Human_RBP_ID_2034554,Human_RBP_ID_3971319,Human_RBP_ID_4959639,Human_RBP_ID_5622532,Human_RBP_ID_22833141,Human_RBP_ID_23071784,Human_RBP_ID_23116913,Human_RBP_ID_26356064 Human_Splice_Rec_919686,Human_Splice_Rec_919687,Human_Splice_Rec_919748,Human_Splice_Rec_919749,Human_Splice_Rec_919756,Human_Splice_Rec_919757 Human_miRNA_ID_2516858 RMVar_hsa_circ_51674,RMVar_hsa_circ_357619,RMVar_hsa_circ_362402,RMVar_hsa_circ_361312,RMVar_hsa_circ_44175,RMVar_hsa_circ_22460,RMVar_hsa_circ_364129,RMVar_hsa_circ_54442,RMVar_hsa_circ_22799,RMVar_hsa_circ_74513,RMVar_hsa_circ_347621,RMVar_hsa_circ_60578,RMVar_hsa_circ_248192,RMVar_hsa_circ_279651,RMVar_hsa_circ_307735,RMVar_hsa_circ_373625,RMVar_hsa_circ_315204,RMVar_hsa_circ_287696,RMVar_hsa_circ_273692 65099 RMVar_ID_65099 Human_SNP_ID_339450595 m1A Human chr7 + 127869164 127869164 127869164 AAGAGTCAGGGAGGCCTCAGTGGCAAGGTATCAGGAGCAAGGACCTGAAGGATGGCAAAAAGCAA AAGAGTCAGGGAGGCCTCAGTGGCAAGGTATCTGGAGCAAGGACCTGAAGGATGGCAAAAAGCAA A T SND1 Ensembl:ENSG00000197157 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:127869146..127869253 26863196 MeRIP-seq:(Medium) rs756546891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15997447 RMVar_hsa_circ_51674,RMVar_hsa_circ_362402,RMVar_hsa_circ_44175,RMVar_hsa_circ_22460,RMVar_hsa_circ_54442,RMVar_hsa_circ_248196,RMVar_hsa_circ_74513,RMVar_hsa_circ_347621,RMVar_hsa_circ_60578,RMVar_hsa_circ_307735,RMVar_hsa_circ_315204,RMVar_hsa_circ_287696,RMVar_hsa_circ_273692,RMVar_hsa_circ_56878,RMVar_hsa_circ_314160,RMVar_hsa_circ_328900,RMVar_hsa_circ_331772,RMVar_hsa_circ_325724,RMVar_hsa_circ_248197,RMVar_hsa_circ_248194,RMVar_hsa_circ_248195 65100 RMVar_ID_65100 Human_SNP_ID_339474688 m1A Human chr7 + 127977844 127977844 127977844 CAAGAGGATGTAGCAATCACTGGGTTATGTGGATAGAGTAGGGAAGAAGATAAGAGAGGTTTTCA CAAGAGGATGTAGCAATCACTGGGTTATGTGGTTAGAGTAGGGAAGAAGATAAGAGAGGTTTTCA A T SND1 Ensembl:ENSG00000197157 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:127977841..127978004 26863196 MeRIP-seq:(Medium) rs1409230121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22623760 RMVar_hsa_circ_22460,RMVar_hsa_circ_54442,RMVar_hsa_circ_347621,RMVar_hsa_circ_315204,RMVar_hsa_circ_56878,RMVar_hsa_circ_325724,RMVar_hsa_circ_248197,RMVar_hsa_circ_248198,RMVar_hsa_circ_327529,RMVar_hsa_circ_358848,RMVar_hsa_circ_329849 65101 RMVar_ID_65101 Human_SNP_ID_339497149 m1A Human chr7 + 128074563 128074563 128074563 GGCCGGCAACTTTATCGGCTGGCTGCACATCGACGGTGCCAACCTGTCCGTCCTGCTGGTGGAGC GGCCGGCAACTTTATCGGCTGGCTGCACATCGCCGGTGCCAACCTGTCCGTCCTGCTGGTGGAGC A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs751602265 Functional Loss SNV dbSNP153 33..33 33 - - - 65102 RMVar_ID_65102 Human_SNP_ID_339499515 m1A Human chr7 - 128084797 128084797 128084797 TTGGCAATGCAGAACTCTCCCCTGCGGGGGGCATAGGAGCCCTCTACAGGGGGGTGACTGGCAAT TTGGCAATGCAGAACTCTCCCCTGCGGGGGGCGTAGGAGCCCTCTACAGGGGGGTGACTGGCAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:128084749..128084850 32194978 MeRIP-seq:(Medium) rs965815156 Functional Loss SNV dbSNP153 33..33 33 - - - 65103 RMVar_ID_65103 Human_SNP_ID_339501259 m1A Human chr7 + 128091879 128091879 128091879 ACCTGAATGCCCAAGAGTCAGCCAAGAGCGCCAGGGTGAGTTCTTACCTTGGGAGCCCCCAGAGG ACCTGAATGCCCAAGAGTCAGCCAAGAGCGCCGGGGTGAGTTCTTACCTTGGGAGCCCCCAGAGG A G SND1 Ensembl:ENSG00000197157 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:128091876..128091900 26863196 MeRIP-seq:(Medium) rs1355732603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8915090,Human_RBP_ID_26831691 Human_Splice_Rec_919710,Human_Splice_Rec_919711,Human_Splice_Rec_919806,Human_Splice_Rec_919807,Human_Splice_Rec_919810,Human_Splice_Rec_919811 RMVar_hsa_circ_76934,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_81641,RMVar_hsa_circ_248208 65104 RMVar_ID_65104 Human_SNP_ID_339559777 m1A Human chr7 - 128336001 128335999 128336002 AGAGCCATGAATCTAAACATCAGGAATCAGTTAAAAAGAAGGGCAGAGAGGAAGAGGATATGGAA AGAGCCATGAATCTAAACATCAGGAATCAGT___AAAGAAGGGCAGAGAGGAAGAGGATATGGAA TTTA T RBM28 Ensembl:ENSG00000106344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128335823..128336002 26863196 MeRIP-seq:(Medium) rs754760143 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_86896,Human_RBP_ID_253203,Human_RBP_ID_4959676,Human_RBP_ID_9350906,Human_RBP_ID_17664882,Human_RBP_ID_23080697,Human_RBP_ID_23116914,Human_RBP_ID_24549031,Human_RBP_ID_26068948,Human_RBP_ID_26357069,Human_RBP_ID_27829809 Human_Splice_Rec_919840,Human_Splice_Rec_919874,Human_Splice_Rec_919902,Human_Splice_Rec_919922,Human_Splice_Rec_919926 RMVar_hsa_circ_61734,RMVar_hsa_circ_71580,RMVar_hsa_circ_22864,RMVar_hsa_circ_347166,RMVar_hsa_circ_350958,RMVar_hsa_circ_65412,RMVar_hsa_circ_364892,RMVar_hsa_circ_248215,RMVar_hsa_circ_360585,RMVar_hsa_circ_72614,RMVar_hsa_circ_326295,RMVar_hsa_circ_248216 65105 RMVar_ID_65105 Human_SNP_ID_339566803 m1A Human chr7 - 128361417 128361417 128361417 CTTCAGTCGGGGCGCTGGGCACAACAGAGAGAAGCGGTGAGATACCACGAAGCGTTGCCCAGCTG CTTCAGTCGGGGCGCTGGGCACAACAGAGAGAGGCGGTGAGATACCACGAAGCGTTGCCCAGCTG T C PRRT4 Ensembl:ENSG00000224940 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128361377..128361487 26863196 MeRIP-seq:(Medium) rs1442536100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_919948,Human_Splice_Rec_919980 65106 RMVar_ID_65106 Human_SNP_ID_339578304 m1A Human chr7 - 128405818 128405818 128405818 GATCAGCGGCGGCACCGGCTACGTGCCCGAGGATGGGCTCACCGCGCAGCAGCTCTTCGCCAGCG GATCAGCGGCGGCACCGGCTACGTGCCCGAGGCTGGGCTCACCGCGCAGCAGCTCTTCGCCAGCG T G IMPDH1 Ensembl:ENSG00000106348 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128405718..128406000 26863196 MeRIP-seq:(Medium) rs780283789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956661,Human_RBP_ID_8150604,Human_RBP_ID_9337361 Human_Splice_Rec_919985,Human_Splice_Rec_920012,Human_Splice_Rec_920013,Human_Splice_Rec_920072,Human_Splice_Rec_920073,Human_Splice_Rec_920097,Human_Splice_Rec_920124,Human_Splice_Rec_920125,Human_Splice_Rec_920154,Human_Splice_Rec_920155,Human_Splice_Rec_920180,Human_Splice_Rec_920181,Human_Splice_Rec_920205,Human_Splice_Rec_920255,Human_Splice_Rec_920307,Human_Splice_Rec_920316,Human_Splice_Rec_920317,Human_Splice_Rec_920326,Human_Splice_Rec_920327 65107 RMVar_ID_65107 Human_SNP_ID_339578323 m1A Human chr7 - 128405857 128405857 128405857 TCGGGTCGCGGGGTCTCGCGGCAGCATGGCGGACTACCTGATCAGCGGCGGCACCGGCTACGTGC TCGGGTCGCGGGGTCTCGCGGCAGCATGGCGGGCTACCTGATCAGCGGCGGCACCGGCTACGTGC T C IMPDH1 Ensembl:ENSG00000106348 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128405776..128405950 26863196 MeRIP-seq:(Medium) rs1219303232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956661,Human_RBP_ID_8150604,Human_RBP_ID_8907463,Human_RBP_ID_16001248,Human_RBP_ID_18414077,Human_RBP_ID_27104727,Human_RBP_ID_27528252 Human_Splice_Rec_919985,Human_Splice_Rec_920012,Human_Splice_Rec_920013,Human_Splice_Rec_920072,Human_Splice_Rec_920073,Human_Splice_Rec_920097,Human_Splice_Rec_920124,Human_Splice_Rec_920125,Human_Splice_Rec_920154,Human_Splice_Rec_920155,Human_Splice_Rec_920180,Human_Splice_Rec_920181,Human_Splice_Rec_920205,Human_Splice_Rec_920255,Human_Splice_Rec_920307,Human_Splice_Rec_920316,Human_Splice_Rec_920317,Human_Splice_Rec_920326,Human_Splice_Rec_920327 65108 RMVar_ID_65108 Human_SNP_ID_339578327 m1A Human chr7 - 128405867 128405867 128405867 GGTGTTTATGTCGGGTCGCGGGGTCTCGCGGCAGCATGGCGGACTACCTGATCAGCGGCGGCACC GGTGTTTATGTCGGGTCGCGGGGTCTCGCGGCGGCATGGCGGACTACCTGATCAGCGGCGGCACC T C IMPDH1 Ensembl:ENSG00000106348 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:128405776..128405975 26863410 MeRIP-seq:(Medium) rs1238921380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956661,Human_RBP_ID_8150604,Human_RBP_ID_8907463,Human_RBP_ID_18414077 65109 RMVar_ID_65109 Human_SNP_ID_339579444 m1A Human chr7 - 128409793 128409793 128409793 ACCCGGGACACGAGACGGCGGCGCAGCGGTACAGCGCCCGACTGCTGCAGGCCGGCTACGAGCCC ACCCGGGACACGAGACGGCGGCGCAGCGGTACTGCGCCCGACTGCTGCAGGCCGGCTACGAGCCC T A IMPDH1 Ensembl:ENSG00000106348 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128409649..128409933 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4956662 Human_Splice_Rec_920039,Human_Splice_Rec_920067,Human_Splice_Rec_920121,Human_Splice_Rec_920149,Human_Splice_Rec_920179,Human_Splice_Rec_920285,Human_Splice_Rec_920299,Human_Splice_Rec_920313,Human_Splice_Rec_920323 65110 RMVar_ID_65110 Human_SNP_ID_339579445 m1A Human chr7 - 128409793 128409793 128409793 ACCCGGGACACGAGACGGCGGCGCAGCGGTACAGCGCCCGACTGCTGCAGGCCGGCTACGAGCCC ACCCGGGACACGAGACGGCGGCGCAGCGGTACCGCGCCCGACTGCTGCAGGCCGGCTACGAGCCC T G IMPDH1 Ensembl:ENSG00000106348 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128409649..128409933 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4956662 Human_Splice_Rec_920039,Human_Splice_Rec_920067,Human_Splice_Rec_920121,Human_Splice_Rec_920149,Human_Splice_Rec_920179,Human_Splice_Rec_920285,Human_Splice_Rec_920299,Human_Splice_Rec_920313,Human_Splice_Rec_920323 65111 RMVar_ID_65111 Human_SNP_ID_339589838 m1A Human chr7 - 128455918 128455918 128455918 TACTAAGCACCAGCGCAGAAGCTTCCCGCCACAAAACTCACCGGAGACAAAAGCGCCGTCAGCCG TACTAAGCACCAGCGCAGAAGCTTCCCGCCACGAAACTCACCGGAGACAAAAGCGCCGTCAGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128455868..128455981 26863196 MeRIP-seq:(Medium) rs1232076218 Functional Loss SNV dbSNP153 33..33 33 - - - 65112 RMVar_ID_65112 Human_SNP_ID_339601698 m1A Human chr7 + 128503458 128503458 128503458 TTAGATGCTTTTTTTTTTTTTTTTTAGGAGACAGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTC TTAGATGCTTTTTTTTTTTTTTTTTAGGAGACGGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1442970940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254472,Human_RBP_ID_794453,Human_RBP_ID_7691333,Human_RBP_ID_16001711,Human_RBP_ID_23196727,Human_RBP_ID_26550789 Human_miRNA_ID_59559,Human_miRNA_ID_977480,Human_miRNA_ID_1591663 65113 RMVar_ID_65113 Human_SNP_ID_339609032 m1A Human chr7 - 128531717 128531706 128531717 CGGCTGCGGGCCGCTCCGCTCTCCCCCTGGGCAGGCCCGGGGCGGAGCCGGGGCCTCCCCTGAGC CGGCTGCGGGCCGCTCCGCTCTCCCCCTGGGC___________GGAGCCGGGGCCTCCCCTGAGC CGCCCCGGGCCT C RF00017-4674 RNACentral:URS000094E2D9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128531670..128531830 26863196 MeRIP-seq:(Medium) rs1031595168 Functional Loss DEL dbSNP153 33..43 33 - - - 65114 RMVar_ID_65114 Human_SNP_ID_339609037 m1A Human chr7 + 128531722 128531722 128531722 GGGGAGGCCCCGGCTCCGCCCCGGGCCTGCCCAGGGGGAGAGCGGAGCGGCCCGCAGCCGGGTCG GGGGAGGCCCCGGCTCCGCCCCGGGCCTGCCCTGGGGGAGAGCGGAGCGGCCCGCAGCCGGGTCG A T lnc-METTL2B-3 RNACentral:URS00009AF195 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128531673..128531858 26863196 MeRIP-seq:(Medium) rs1430216492 Functional Loss SNV dbSNP153 33..33 33 - - - 65115 RMVar_ID_65115 Human_SNP_ID_339609052 m1A Human chr7 - 128531752 128531747 128531752 TCCACGCTCCTCCCGGGAGGGGCCCCGACCCGACCCGGCTGCGGGCCGCTCCGCTCTCCCCCTGG TCCACGCTCCTCCCGGGAGGGGCCCCGACCCG_____GCTGCGGGCCGCTCCGCTCTCCCCCTGG CCGGGT C RF00017-4674 RNACentral:URS000094E2D9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128531702..128531901 26863196 MeRIP-seq:(Medium) rs1205788410 Functional Loss DEL dbSNP153 33..37 33 - - - 65116 RMVar_ID_65116 Human_SNP_ID_339638069 m1A Human chr7 + 128651318 128651318 128651318 CCTACGTCACGGCAGTCTCCGCAGATGAGCCTACTGCCCCACAACAGCCTCCACAGGCACAGCTC CCTACGTCACGGCAGTCTCCGCAGATGAGCCTCCTGCCCCACAACAGCCTCCACAGGCACAGCTC A C AC018638.4 Ensembl:ENSG00000243302 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128651192..128651355 26863196 MeRIP-seq:(Medium) rs1424054759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954922,Human_RBP_ID_1691219,Human_RBP_ID_3867723,Human_RBP_ID_5090696,Human_RBP_ID_5222200,Human_RBP_ID_5657811,Human_RBP_ID_8915469,Human_RBP_ID_10370392,Human_RBP_ID_17316504,Human_RBP_ID_17429616,Human_RBP_ID_17543674,Human_RBP_ID_19139610,Human_RBP_ID_21558048,Human_RBP_ID_21960810,Human_RBP_ID_21994439 65117 RMVar_ID_65117 Human_SNP_ID_339638074 m1A Human chr7 + 128651326 128651326 128651326 ACGGCAGTCTCCGCAGATGAGCCTACTGCCCCACAACAGCCTCCACAGGCACAGCTCCATCGTTA ACGGCAGTCTCCGCAGATGAGCCTACTGCCCCCCAACAGCCTCCACAGGCACAGCTCCATCGTTA A C AC018638.4 Ensembl:ENSG00000243302 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:128651276..128651350 26863196 MeRIP-seq:(Medium) rs1488865170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954922,Human_RBP_ID_1691219,Human_RBP_ID_3867723,Human_RBP_ID_5090696,Human_RBP_ID_5222200,Human_RBP_ID_5657811,Human_RBP_ID_8915469,Human_RBP_ID_10370392,Human_RBP_ID_17316504,Human_RBP_ID_17429616,Human_RBP_ID_21558048,Human_RBP_ID_21960810,Human_RBP_ID_21994439 65118 RMVar_ID_65118 Human_SNP_ID_339638178 m1A Human chr7 + 128651563 128651562 128651563 AGTCCCAACATCTGCCTCACAGCAGATTCTTCACGCCCAGCATCTGCCTCACTGTGGACCCCCCA AGTCCCAACATCTGCCTCACAGCAGATTCTTC_CGCCCAGCATCTGCCTCACTGTGGACCCCCCA CA C AC018638.4 Ensembl:ENSG00000243302 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128651531..128651603 26863196 MeRIP-seq:(Medium) rs1563081558 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3867724,Human_RBP_ID_8273221,Human_RBP_ID_8915363,Human_RBP_ID_9312190,Human_RBP_ID_17093819,Human_RBP_ID_17200441,Human_RBP_ID_17316505,Human_RBP_ID_17431258,Human_RBP_ID_17543675,Human_RBP_ID_17578369,Human_RBP_ID_17585968,Human_RBP_ID_18172403,Human_RBP_ID_21395624,Human_RBP_ID_21960811,Human_RBP_ID_21994323,Human_RBP_ID_26069800,Human_RBP_ID_27104791 Human_miRNA_ID_1842031 65119 RMVar_ID_65119 Human_SNP_ID_339638765 m1A Human chr7 + 128653327 128653327 128653327 GCCCAGCTCCCAACCGCCTTTCTAGGCCCCGAACTTTCTCCAGCCAAGCTCTGAGGGCCCACCTC GCCCAGCTCCCAACCGCCTTTCTAGGCCCCGAGCTTTCTCCAGCCAAGCTCTGAGGGCCCACCTC A G LINC01000,LINC01000:2 RNACentral:URS00008C0C4E,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:128653276..128653375 26863196 MeRIP-seq:(Medium) rs1255506639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27528277 65120 RMVar_ID_65120 Human_SNP_ID_339660291 m1A Human chr7 + 128739404 128739404 128739404 AGCTGAGCCGGTGGGTGAGCGGCGGCCACGGCATCCTGTGCTGTGGGGGCTACGAGGAAAGGTAA AGCTGAGCCGGTGGGTGAGCGGCGGCCACGGCGTCCTGTGCTGTGGGGGCTACGAGGAAAGGTAA A G CALU Ensembl:ENSG00000128595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128739351..128739487 26863196 MeRIP-seq:(Medium) rs911195557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87066,Human_RBP_ID_254271,Human_RBP_ID_674616,Human_RBP_ID_795038,Human_RBP_ID_4923975,Human_RBP_ID_5328015,Human_RBP_ID_5622547,Human_RBP_ID_8915093,Human_RBP_ID_9337365 Human_Splice_Rec_920601,Human_Splice_Rec_920611,Human_Splice_Rec_920625,Human_Splice_Rec_920637,Human_Splice_Rec_920649 65121 RMVar_ID_65121 Human_SNP_ID_339660292 m1A Human chr7 + 128739404 128739404 128739404 AGCTGAGCCGGTGGGTGAGCGGCGGCCACGGCATCCTGTGCTGTGGGGGCTACGAGGAAAGGTAA AGCTGAGCCGGTGGGTGAGCGGCGGCCACGGCTTCCTGTGCTGTGGGGGCTACGAGGAAAGGTAA A T CALU Ensembl:ENSG00000128595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128739351..128739487 26863196 MeRIP-seq:(Medium) rs911195557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87066,Human_RBP_ID_254271,Human_RBP_ID_674616,Human_RBP_ID_795038,Human_RBP_ID_4923975,Human_RBP_ID_5328015,Human_RBP_ID_5622547,Human_RBP_ID_8915093,Human_RBP_ID_9337365 Human_Splice_Rec_920601,Human_Splice_Rec_920611,Human_Splice_Rec_920625,Human_Splice_Rec_920637,Human_Splice_Rec_920649 65122 RMVar_ID_65122 Human_SNP_ID_339660295 m1A Human chr7 - 128739408 128739408 128739408 GTACTTACCTTTCCTCGTAGCCCCCACAGCACAGGATGCCGTGGCCGCCGCTCACCCACCGGCTC GTACTTACCTTTCCTCGTAGCCCCCACAGCACGGGATGCCGTGGCCGCCGCTCACCCACCGGCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128739351..128739504 26863196 MeRIP-seq:(Medium) rs1276278704 Functional Loss SNV dbSNP153 33..33 33 - - - 65123 RMVar_ID_65123 Human_SNP_ID_339660296 m1A Human chr7 - 128739408 128739408 128739408 GTACTTACCTTTCCTCGTAGCCCCCACAGCACAGGATGCCGTGGCCGCCGCTCACCCACCGGCTC GTACTTACCTTTCCTCGTAGCCCCCACAGCACCGGATGCCGTGGCCGCCGCTCACCCACCGGCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128739351..128739504 26863196 MeRIP-seq:(Medium) rs1276278704 Functional Loss SNV dbSNP153 33..33 33 - - - 65124 RMVar_ID_65124 Human_SNP_ID_339660306 m1A Human chr7 - 128739434 128739434 128739434 CAGTGGTGAAGGGGCTGGGCATCACCGTACTTACCTTTCCTCGTAGCCCCCACAGCACAGGATGC CAGTGGTGAAGGGGCTGGGCATCACCGTACTTCCCTTTCCTCGTAGCCCCCACAGCACAGGATGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128739351..128739492 26863196 MeRIP-seq:(Medium) rs1385343724 Functional Loss SNV dbSNP153 33..33 33 - - - 65125 RMVar_ID_65125 Human_SNP_ID_339662481 m1A Human chr7 - 128748620 128748620 128748620 TTCTGTGGGTTTGCTCAAGGCAAAGGCTGTGCACAGGGACAGGCACATAAGAAACTGTCGCAGGT TTCTGTGGGTTTGCTCAAGGCAAAGGCTGTGCCCAGGGACAGGCACATAAGAAACTGTCGCAGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128748551..128748625 26863196 MeRIP-seq:(Medium) rs1458233349 Functional Loss SNV dbSNP153 33..33 33 - - - 65126 RMVar_ID_65126 Human_SNP_ID_339663804 m1A Human chr7 + 128754229 128754229 128754229 CCTGGCTAAGTCCAGAGTTCTGTGTCTTTTTAACCTTTTGCTGGATTTCTCTGCATTTTCTACAG CCTGGCTAAGTCCAGAGTTCTGTGTCTTTTTATCCTTTTGCTGGATTTCTCTGCATTTTCTACAG A T CALU Ensembl:ENSG00000128595 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128754228..128754564 26863196 MeRIP-seq:(Medium) rs1184816162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16003494 RMVar_hsa_circ_337851,RMVar_hsa_circ_351004,RMVar_hsa_circ_248241 65127 RMVar_ID_65127 Human_SNP_ID_339665018 m1A Human chr7 + 128758944 128758944 128758944 ATGGTTAGAGATGAGCGGAGGTTTAAAATGGCAGACAAGGATGGAGACCTCATTGCCACCAAGGA ATGGTTAGAGATGAGCGGAGGTTTAAAATGGCGGACAAGGATGGAGACCTCATTGCCACCAAGGA A G CALU Ensembl:ENSG00000128595 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128758894..128759074 26863196 MeRIP-seq:(Medium) rs201527879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84589,Human_RBP_ID_8907495,Human_RBP_ID_9263511,Human_RBP_ID_16003544,Human_RBP_ID_17199274,Human_RBP_ID_18108174,Human_RBP_ID_22407067,Human_RBP_ID_22774764,Human_RBP_ID_24514699,Human_RBP_ID_27104916 Human_Splice_Rec_920606,Human_Splice_Rec_920607,Human_Splice_Rec_920618,Human_Splice_Rec_920619,Human_Splice_Rec_920630,Human_Splice_Rec_920631,Human_Splice_Rec_920642,Human_Splice_Rec_920643,Human_Splice_Rec_920656,Human_Splice_Rec_920657,Human_Splice_Rec_920663 Human_miRNA_ID_1010292,Human_miRNA_ID_2455291,Human_miRNA_ID_2490121,Human_miRNA_ID_2752206 RMVar_hsa_circ_337851,RMVar_hsa_circ_248241,RMVar_hsa_circ_362864,RMVar_hsa_circ_302470,RMVar_hsa_circ_248243 65128 RMVar_ID_65128 Human_SNP_ID_339665036 m1A Human chr7 - 128759001 128759001 128759001 ACTACTATATCTTTCATGTAGTCATACTCCTCAGGGTGCAGGAAAGCTGTGAACTCCTCCTTGGT ACTACTATATCTTTCATGTAGTCATACTCCTCGGGGTGCAGGAAAGCTGTGAACTCCTCCTTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128758976..128759000 26863196 MeRIP-seq:(Medium) rs749617756 Functional Loss SNV dbSNP153 33..33 33 - - - 65129 RMVar_ID_65129 Human_SNP_ID_339667138 m1A Human chr7 + 128767623 128767623 128767623 CCTCAGACTATGATCATGCAGAGGCAGAAGCCAGGCACCTGGTCTATGAATCAGACCAAAACAAG CCTCAGACTATGATCATGCAGAGGCAGAAGCCGGGCACCTGGTCTATGAATCAGACCAAAACAAG A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:128767451..128767675 32194978 MeRIP-seq:(Medium) rs1445060646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84595,Human_RBP_ID_253391,Human_RBP_ID_674640,Human_RBP_ID_793410,Human_RBP_ID_956413,Human_RBP_ID_7691930,Human_RBP_ID_8915096,Human_RBP_ID_16003689,Human_RBP_ID_17427124,Human_RBP_ID_22407072,Human_RBP_ID_22464757,Human_RBP_ID_22774498,Human_RBP_ID_26831694 Human_Splice_Rec_920623,Human_Splice_Rec_920635,Human_Splice_Rec_920647,Human_Splice_Rec_920661,Human_Splice_Rec_920667 Human_miRNA_ID_247027,Human_miRNA_ID_249562,Human_miRNA_ID_338529,Human_miRNA_ID_795726,Human_miRNA_ID_2534326,Human_miRNA_ID_2536059 RMVar_hsa_circ_97215,RMVar_hsa_circ_248245,RMVar_hsa_circ_81132,RMVar_hsa_circ_248244,RMVar_hsa_circ_348140 65130 RMVar_ID_65130 Human_SNP_ID_339667794 m1A Human chr7 + 128770203 128770202 128770203 GAATGGGAATTCTCTTAAGAAACCCTGAGATTAAAAAAAGACTATTTGGATAACTTATAGGAAAG GAATGGGAATTCTCTTAAGAAACCCTGAGATT_AAAAAAGACTATTTGGATAACTTATAGGAAAG TA T CALU Ensembl:ENSG00000128595 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1562884700 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_674678,Human_RBP_ID_7692003,Human_RBP_ID_16003809,Human_RBP_ID_17311466,Human_RBP_ID_17424032,Human_RBP_ID_18378027,Human_RBP_ID_23196822,Human_RBP_ID_27763563 Human_miRNA_ID_2230668 RMVar_hsa_circ_248245,RMVar_hsa_circ_81132 65131 RMVar_ID_65131 Human_SNP_ID_339673921 m1A Human chr7 + 128794403 128794391 128794403 TATGAGGAGGAAGAGGAAGAGGAAGAGGAGGAAGAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA TATGAGGAGGAAGAGGAAGAG____________GAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA GGAAGAGGAGGAA G CCDC136 Ensembl:ENSG00000128596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128794323..128794537 26863196 MeRIP-seq:(Medium) rs751367998 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_14573,Human_RBP_ID_1690977,Human_RBP_ID_3971362,Human_RBP_ID_18414232,Human_RBP_ID_22621467,Human_RBP_ID_22685896,Human_RBP_ID_23080161,Human_RBP_ID_24549032,Human_RBP_ID_26358326,Human_RBP_ID_27829820 Human_Splice_Rec_920682,Human_Splice_Rec_920692,Human_Splice_Rec_920698,Human_Splice_Rec_920716,Human_Splice_Rec_920736,Human_Splice_Rec_920738,Human_Splice_Rec_920772 65132 RMVar_ID_65132 Human_SNP_ID_339673924 m1A Human chr7 + 128794403 128794400 128794403 TATGAGGAGGAAGAGGAAGAGGAAGAGGAGGAAGAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA TATGAGGAGGAAGAGGAAGAGGAAGAGGAG___GAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA GGAA G CCDC136 Ensembl:ENSG00000128596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128794323..128794537 26863196 MeRIP-seq:(Medium) rs774361033 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_14573,Human_RBP_ID_1690977,Human_RBP_ID_3971362,Human_RBP_ID_18414232,Human_RBP_ID_22621467,Human_RBP_ID_22685896,Human_RBP_ID_23080161,Human_RBP_ID_24549032,Human_RBP_ID_26358326,Human_RBP_ID_27829820 Human_Splice_Rec_920682,Human_Splice_Rec_920692,Human_Splice_Rec_920698,Human_Splice_Rec_920716,Human_Splice_Rec_920736,Human_Splice_Rec_920738,Human_Splice_Rec_920772 65133 RMVar_ID_65133 Human_SNP_ID_339682808 m1A Human chr7 + 128830525 128830520 128830525 CCCCGCCAGCCCCGGCGCGAGAGAAGTTGGAGAGGAGAGCAGCGCAGCGCAGCGAGTCCCGTGGT CCCCGCCAGCCCCGGCGCGAGAGAAGTT_____GGAGAGCAGCGCAGCGCAGCGAGTCCCGTGGT TGGAGA T FLNC Ensembl:ENSG00000128591 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:128830476..128830600 32194978 MeRIP-seq:(Medium) rs1172751451 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_84526,Human_RBP_ID_4956670 RMVar_hsa_circ_248249,RMVar_hsa_circ_81402,RMVar_hsa_circ_108988,RMVar_hsa_circ_109058,RMVar_hsa_circ_121130,RMVar_hsa_circ_105263,RMVar_hsa_circ_248251,RMVar_hsa_circ_248252,RMVar_hsa_circ_248253,RMVar_hsa_circ_248250 65134 RMVar_ID_65134 Human_SNP_ID_339684799 m1A Human chr7 + 128837465 128837465 128837465 GGATGAGCATTCTGTTATGACCTACCTGTCCCAGTTCCCCAAGGCCAAGCTCAAACCTGGTGCCC GGATGAGCATTCTGTTATGACCTACCTGTCCCGGTTCCCCAAGGCCAAGCTCAAACCTGGTGCCC A G FLNC Ensembl:ENSG00000128591 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:128830726..128843827 32194978 MeRIP-seq:(Medium) rs760009430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84530,Human_RBP_ID_9263514,Human_RBP_ID_18196074,Human_RBP_ID_22464760 Human_Splice_Rec_920872,Human_Splice_Rec_920873,Human_Splice_Rec_920964,Human_Splice_Rec_920965 RMVar_hsa_circ_248249,RMVar_hsa_circ_81402,RMVar_hsa_circ_108988,RMVar_hsa_circ_109058,RMVar_hsa_circ_121130,RMVar_hsa_circ_105263,RMVar_hsa_circ_248251,RMVar_hsa_circ_248252,RMVar_hsa_circ_248253,RMVar_hsa_circ_248250,RMVar_hsa_circ_76545,RMVar_hsa_circ_248254,RMVar_hsa_circ_372383,RMVar_hsa_circ_126255,RMVar_hsa_circ_248255,RMVar_hsa_circ_248256,RMVar_hsa_circ_376817 65135 RMVar_ID_65135 Human_SNP_ID_339685719 m1A Human chr7 - 128840162 128840158 128840162 CCCCACCCTCACGACCCTGGGCTCTGGCACTCACTTGGCCCCTTGACCGTGACCTTGAGCTCCCC CCCCACCCTCACGACCCTGGGCTCTGGCACTC____GGCCCCTTGACCGTGACCTTGAGCTCCCC CAAGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128840146..128840230 26863196 MeRIP-seq:(Medium) rs763330423 Functional Loss DEL dbSNP153 33..36 33 - - - Clinvar_Rec_261 65136 RMVar_ID_65136 Human_SNP_ID_339685722 m1A Human chr7 - 128840162 128840162 128840162 CCCCACCCTCACGACCCTGGGCTCTGGCACTCACTTGGCCCCTTGACCGTGACCTTGAGCTCCCC CCCCACCCTCACGACCCTGGGCTCTGGCACTCTCTTGGCCCCTTGACCGTGACCTTGAGCTCCCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128840146..128840230 26863196 MeRIP-seq:(Medium) rs111806457 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_262 65137 RMVar_ID_65137 Human_SNP_ID_339685723 m1A Human chr7 - 128840162 128840162 128840162 CCCCACCCTCACGACCCTGGGCTCTGGCACTCACTTGGCCCCTTGACCGTGACCTTGAGCTCCCC CCCCACCCTCACGACCCTGGGCTCTGGCACTCCCTTGGCCCCTTGACCGTGACCTTGAGCTCCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128840146..128840230 26863196 MeRIP-seq:(Medium) rs111806457 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_262 65138 RMVar_ID_65138 Human_SNP_ID_339686069 m1A Human chr7 - 128841142 128841142 128841142 GAAGCCTGGGGCAAGGTGGGGGAGGGTCGGGGATCCAGCATCAGGCAAGACCCTTCCGTCCCCCA GAAGCCTGGGGCAAGGTGGGGGAGGGTCGGGGGTCCAGCATCAGGCAAGACCCTTCCGTCCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128841140..128841315 26863196 MeRIP-seq:(Medium) rs2291565 Functional Loss SNV dbSNP153 33..33 33 - - - 65139 RMVar_ID_65139 Human_SNP_ID_339691937 m1A Human chr7 - 128858106 128858106 128858106 CTTGCTGGCATCTGAGGAGAACTTGGGGATGGAGCTGTAGCTGGAGCCCCGGCTTGAGGAGGACT CTTGCTGGCATCTGAGGAGAACTTGGGGATGGTGCTGTAGCTGGAGCCCCGGCTTGAGGAGGACT T A FLNC-AS1 Ensembl:ENSG00000242902 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:128858051..128858150 32194978 MeRIP-seq:(Medium) rs774081954 Functional Loss SNV dbSNP153 33..33 33 - - - 65140 RMVar_ID_65140 Human_SNP_ID_339693239 m1A Human chr7 - 128862927 128862927 128862927 CAGTCACCGTGTCCTCGTCTCCGATCACTGCGATGAGCTTACCCCTCCCCGCCATCCCTGCAGCC CAGTCACCGTGTCCTCGTCTCCGATCACTGCGGTGAGCTTACCCCTCCCCGCCATCCCTGCAGCC T C KCP Ensembl:ENSG00000135253 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:128862848..128863102;chr7:128862851..128863106;chr7:128862851..128863075;chr7:128862851..128863109 26863196 MeRIP-seq:(Medium) rs1804887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_921078 65141 RMVar_ID_65141 Human_SNP_ID_339693929 m1A Human chr7 - 128865479 128865479 128865479 TATGGGTGCTCCTTGGAGGGGATCTCCAGGACAGCGGGGATGGACTGCTGGTGGGCGTCCAGGGC TATGGGTGCTCCTTGGAGGGGATCTCCAGGACGGCGGGGATGGACTGCTGGTGGGCGTCCAGGGC T C KCP Ensembl:ENSG00000135253 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:128865353..128865800;chr7:128865341..128865660 26863196 MeRIP-seq:(Medium) rs767465115 Functional Loss SNV dbSNP153 33..33 33 - - - 65142 RMVar_ID_65142 Human_SNP_ID_339697300 m1A Human chr7 - 128877702 128877702 128877702 GTGCCGGGCAGCAGGTTACCGTGCCAGGCGTGAGGCCAATGCCCGGTGTGGGGTGCTGAAGTCCT GTGCCGGGCAGCAGGTTACCGTGCCAGGCGTGGGGCCAATGCCCGGTGTGGGGTGCTGAAGTCCT T C KCP Ensembl:ENSG00000135253 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128877673..128877767 26863196 MeRIP-seq:(Medium) rs1345009768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_921086,Human_Splice_Rec_921168,Human_Splice_Rec_921242,Human_Splice_Rec_921314,Human_Splice_Rec_921382 65143 RMVar_ID_65143 Human_SNP_ID_339701775 m1A Human chr7 + 128891013 128891013 128891013 CACGGAGCCGTCGAGGCAGAGGCAGCGGCGGCAGGGATCGCCGGGCGGGGAGAAGTACTCCTGGT CACGGAGCCGTCGAGGCAGAGGCAGCGGCGGCGGGGATCGCCGGGCGGGGAGAAGTACTCCTGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:128890914..128891260;chr7:128890928..128891156 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 65144 RMVar_ID_65144 Human_SNP_ID_339701776 m1A Human chr7 + 128891013 128891013 128891013 CACGGAGCCGTCGAGGCAGAGGCAGCGGCGGCAGGGATCGCCGGGCGGGGAGAAGTACTCCTGGT CACGGAGCCGTCGAGGCAGAGGCAGCGGCGGCTGGGATCGCCGGGCGGGGAGAAGTACTCCTGGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:128890914..128891260;chr7:128890928..128891156 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 65145 RMVar_ID_65145 Human_SNP_ID_339718713 m1A Human chr7 - 128954409 128954409 128954409 TGTGTGGAGAAAAAATGTTTACAGGGCTAACAAGGGATGATGTGTCATTTAGTATGTTACTAAAA TGTGTGGAGAAAAAATGTTTACAGGGCTAACACGGGATGATGTGTCATTTAGTATGTTACTAAAA T G TNPO3 Ensembl:ENSG00000064419 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128954276..128954418 26863196 MeRIP-seq:(Medium) rs1274927899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_674831,Human_RBP_ID_1050333,Human_RBP_ID_1397365,Human_RBP_ID_4924235,Human_RBP_ID_5123113,Human_RBP_ID_7692201,Human_RBP_ID_8218520,Human_RBP_ID_8907573,Human_RBP_ID_9204191,Human_RBP_ID_16004179,Human_RBP_ID_18091897,Human_RBP_ID_18378093,Human_RBP_ID_24189201,Human_RBP_ID_26550825 65146 RMVar_ID_65146 Human_SNP_ID_339722331 m1A Human chr7 - 128970314 128970314 128970314 TTATCTGATGTTCCTGCTTTCCTACATACAGCATGAAGAAGACTTTGAATTACGGAAAGAACTGA TTATCTGATGTTCCTGCTTTCCTACATACAGCGTGAAGAAGACTTTGAATTACGGAAAGAACTGA T C TNPO3 Ensembl:ENSG00000064419 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:128970277..128972537 32194978 MeRIP-seq:(Medium) rs764906042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3054996,Human_RBP_ID_9312003,Human_RBP_ID_22685938 Human_Splice_Rec_921692,Human_Splice_Rec_921736,Human_Splice_Rec_921782,Human_Splice_Rec_921824,Human_Splice_Rec_921868 RMVar_hsa_circ_12346,RMVar_hsa_circ_268521,RMVar_hsa_circ_361133,RMVar_hsa_circ_375946,RMVar_hsa_circ_265082,RMVar_hsa_circ_248301,RMVar_hsa_circ_308183,RMVar_hsa_circ_332248,RMVar_hsa_circ_351871,RMVar_hsa_circ_248299,RMVar_hsa_circ_371823,RMVar_hsa_circ_347852,RMVar_hsa_circ_328720,RMVar_hsa_circ_330044,RMVar_hsa_circ_324129,RMVar_hsa_circ_54838,RMVar_hsa_circ_281204,RMVar_hsa_circ_248303,RMVar_hsa_circ_248304,RMVar_hsa_circ_248302,RMVar_hsa_circ_30676,RMVar_hsa_circ_361311,RMVar_hsa_circ_248300,RMVar_hsa_circ_346514,RMVar_hsa_circ_28115 65147 RMVar_ID_65147 Human_SNP_ID_339741724 m1A Human chr7 - 129054724 129054724 129054724 GCCGACATTGCAGCTCGTGTACCAGGCAGTGCAGGCGCTTTACCACGACCCAGATCCCAGCGGAA GCCGACATTGCAGCTCGTGTACCAGGCAGTGCGGGCGCTTTACCACGACCCAGATCCCAGCGGAA T C TNPO3 Ensembl:ENSG00000064419 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:129054675..129054974 32194978 MeRIP-seq:(Medium) rs1001798611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9403875 Human_Splice_Rec_921655,Human_Splice_Rec_921699,Human_Splice_Rec_921743,Human_Splice_Rec_921789,Human_Splice_Rec_921831 Human_miRNA_ID_2795702,Human_miRNA_ID_2796120,Human_miRNA_ID_2796535,Human_miRNA_ID_2796950,Human_miRNA_ID_2799299 RMVar_hsa_circ_88277,RMVar_hsa_circ_248347 65148 RMVar_ID_65148 Human_SNP_ID_339741747 m1A Human chr7 - 129054773 129054773 129054773 TCAGAGCCGTCGCTACCGCCACTACCGCCACCACCATGGAAGGAGCAAAGCCGACATTGCAGCTC TCAGAGCCGTCGCTACCGCCACTACCGCCACCGCCATGGAAGGAGCAAAGCCGACATTGCAGCTC T C TNPO3 Ensembl:ENSG00000064419 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:129054724..129054875 32194978 MeRIP-seq:(Medium) rs1235547816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18875638,Human_RBP_ID_26357114 RMVar_hsa_circ_88277,RMVar_hsa_circ_248347 65149 RMVar_ID_65149 Human_SNP_ID_339741788 m1A Human chr7 - 129054858 129054858 129054858 AGATGGCGCCAGTCAGGGAGCGGCCGTGGCCCAGACAGTGAGGAAGCGCGAAGGCGGAGCAACCG AGATGGCGCCAGTCAGGGAGCGGCCGTGGCCCGGACAGTGAGGAAGCGCGAAGGCGGAGCAACCG T C TNPO3 Ensembl:ENSG00000064419 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:129054676..129055100;chr7:129054712..129055096;chr7:129054701..129055076;chr7:129054726..129054900 26863196 MeRIP-seq:(Medium) rs1331152744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792805,Human_RBP_ID_842717,Human_RBP_ID_4924357,Human_RBP_ID_9337991,Human_RBP_ID_26357114 Human_miRNA_ID_2998400 RMVar_hsa_circ_88277,RMVar_hsa_circ_248347 65150 RMVar_ID_65150 Human_SNP_ID_339763709 m1A Human chr7 - 129144818 129144818 129144818 GCGGCGGGAGGCGCCCGAGCCGGGGGGCCGGGAGCGGCGCGGGCCGGGGAACCGCGCCTGGAGCT GCGGCGGGAGGCGCCCGAGCCGGGGGGCCGGGTGCGGCGCGGGCCGGGGAACCGCGCCTGGAGCT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:129144726..129145019 26863410 MeRIP-seq:(Medium) rs1383108126 Functional Loss SNV dbSNP153 33..33 33 - - - 65151 RMVar_ID_65151 Human_SNP_ID_339783923 m1A Human chr7 - 129225106 129225106 129225106 TCCTTCAGCTCCACCTCAGGCACCTTGGCGGCAGCCGCGGCTGACACAACCTGCACCGACATCAC TCCTTCAGCTCCACCTCAGGCACCTTGGCGGCGGCCGCGGCTGACACAACCTGCACCGACATCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:129224990..129225222 26863196 MeRIP-seq:(Medium) rs753132099 Functional Loss SNV dbSNP153 33..33 33 - - - 65152 RMVar_ID_65152 Human_SNP_ID_339783937 m1A Human chr7 + 129225135 129225132 129225135 GGCTGCCGCCAAGGTGCCTGAGGTGGAGCTGAAGGACCTGAGCCCCTCCGAGGCGGAGTCGCAAC GGCTGCCGCCAAGGTGCCTGAGGTGGAGCT___GGACCTGAGCCCCTCCGAGGCGGAGTCGCAAC TGAA T AHCYL2 Ensembl:ENSG00000158467 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129224988..129225464 26863196 MeRIP-seq:(Medium) rs1252068343 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4924619,Human_RBP_ID_9403880,Human_RBP_ID_18466641 RMVar_hsa_circ_112998,RMVar_hsa_circ_248368 65153 RMVar_ID_65153 Human_SNP_ID_339794252 m1A Human chr7 - 129267713 129267713 129267713 CCTATCTTAGGGTCAGGTCCTTATCCTCTCTTACTTAGATAATTACAATAGCCTGATTATTCTCT CCTATCTTAGGGTCAGGTCCTTATCCTCTCTTCCTTAGATAATTACAATAGCCTGATTATTCTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129267706..129267771 26863196 MeRIP-seq:(Medium) rs1184938675 Functional Loss SNV dbSNP153 33..33 33 - - - 65154 RMVar_ID_65154 Human_SNP_ID_339837486 m1A Human chr7 + 129461839 129461837 129461839 TGTGAGGTCAAGGGGAGGATGTTTTATAGCTGAGAGATACTAGAGCATTTTTTGTTTCCTAAAAT TGTGAGGTCAAGGGGAGGATGTTTTATAGCT__GAGATACTAGAGCATTTTTTGTTTCCTAAAAT TGA T STRIP2 Ensembl:ENSG00000128578 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129461682..129461886 26863196 MeRIP-seq:(Medium) rs771692505 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26071429 RMVar_hsa_circ_4161,RMVar_hsa_circ_120471,RMVar_hsa_circ_248383,RMVar_hsa_circ_90313,RMVar_hsa_circ_92815,RMVar_hsa_circ_248385,RMVar_hsa_circ_248387,RMVar_hsa_circ_42136 65155 RMVar_ID_65155 Human_SNP_ID_339843661 m1A Human chr7 + 129488024 129488024 129488024 ACATCATTTTTTTCCACAGACTTGCTGGGACTAGCTTTCAGGTATTGACAGCCAGCCCCATATAT ACATCATTTTTTTCCACAGACTTGCTGGGACTGGCTTTCAGGTATTGACAGCCAGCCCCATATAT A G STRIP2 Ensembl:ENSG00000128578 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3173904 Functional Loss SNV dbSNP153 33..33 33 - - - 65156 RMVar_ID_65156 Human_SNP_ID_339874376 m1A Human chr7 - 129611594 129611594 129611594 AGGAGGTCGGCGCGGCTGTGCTGCGGGCAGGCAGCGGAGAGGGCTCGCGGCGAGGGCTCCAGCTT AGGAGGTCGGCGCGGCTGTGCTGCGGGCAGGCGGCGGAGAGGGCTCGCGGCGAGGGCTCCAGCTT T C AC078846.1 Ensembl:ENSG00000273329 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr7:129611482..129611628;chr7:129611523..129611608;chr7:129611452..129611627 26863196,26863410,26863196 MeRIP-seq:(Medium) rs907845521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4924728,Human_RBP_ID_18426092,Human_RBP_ID_19021474 65157 RMVar_ID_65157 Human_SNP_ID_339874385 m1A Human chr7 + 129611605 129611605 129611605 CTCGCCGCGAGCCCTCTCCGCTGCCTGCCCGCAGCACAGCCGCGCCGACCTCCTCATCATGGCGG CTCGCCGCGAGCCCTCTCCGCTGCCTGCCCGCGGCACAGCCGCGCCGACCTCCTCATCATGGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:129611320..129611631;chr7:129611417..129611621 26863196 MeRIP-seq:(Medium) rs1464560053 Functional Loss SNV dbSNP153 33..33 33 - - - 65158 RMVar_ID_65158 Human_SNP_ID_339874470 m1A Human chr7 - 129611785 129611785 129611785 CGGCTGCGCTACCGTGGGCCTGCGCCGTGGAGACTGCGACCGCGCCGGCTCCTCGCAGCCTCCTG CGGCTGCGCTACCGTGGGCCTGCGCCGTGGAGCCTGCGACCGCGCCGGCTCCTCGCAGCCTCCTG T G RF00017-4495,RF00017-4692,RF00017-4489 RNACentral:URS0000923EDC,RNACentral:URS000090D53C,RNACentral:URS00009982F9 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129611735..129611863 26863196 MeRIP-seq:(Medium) rs1262268541 Functional Loss SNV dbSNP153 33..33 33 - - - 65159 RMVar_ID_65159 Human_SNP_ID_339874516 m1A Human chr7 + 129611922 129611922 129611922 CCGCCGGCCGGCCGGCCCGCCCCGCAGCCGGCACCCTGCCGCCCCCGGCTCTGGGCCTGGGCCCC CCGCCGGCCGGCCGGCCCGCCCCGCAGCCGGCGCCCTGCCGCCCCCGGCTCTGGGCCTGGGCCCC A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:129611872..129612015 26863196 MeRIP-seq:(Medium) rs1247756705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5243320,Human_RBP_ID_9337373 65160 RMVar_ID_65160 Human_SNP_ID_339897846 m1A Human chr7 - 129706259 129706259 129706259 ACCTACATAGCTCCAATGCTCAAAACACCTCCAAATGTCTTTTAACTATGGCAACTAAACTAGAT ACCTACATAGCTCCAATGCTCAAAACACCTCCGAATGTCTTTTAACTATGGCAACTAAACTAGAT T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:129706075..129706524 26863196 MeRIP-seq:(Medium) rs796846174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22011516 65161 RMVar_ID_65161 Human_SNP_ID_339916357 m1A Human chr7 - 129780670 129780670 129780670 CAGCCTTGAGCACCTTTCTGCGGGGAGACTGCAGAGATCGTCCAGTGGCCCTACGGTGCGCCCCA CAGCCTTGAGCACCTTTCTGCGGGGAGACTGCGGAGATCGTCCAGTGGCCCTACGGTGCGCCCCA T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129780623..129780726 26863196 MeRIP-seq:(Medium) rs1440069776 Functional Loss SNV dbSNP153 33..33 33 - - - 65162 RMVar_ID_65162 Human_SNP_ID_339927567 m1A Human chr7 - 129825506 129825506 129825506 GCCTCACACACCGCTAGGAGGGGGCATCCTGGAGCAGGGGGCTGGATCAGGACCCGGCTGGATGG GCCTCACACACCGCTAGGAGGGGGCATCCTGGGGCAGGGGGCTGGATCAGGACCCGGCTGGATGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129825456..129825521 26863196 MeRIP-seq:(Medium) rs1290725312 Functional Loss SNV dbSNP153 33..33 33 - - - 65163 RMVar_ID_65163 Human_SNP_ID_339929344 m1A Human chr7 + 129832462 129832462 129832462 TTCATCACACACACTTAGATGGACACACACACACTCTCGCTCACACTCTCACACATGTGCACACA TTCATCACACACACTTAGATGGACACACACACTCTCTCGCTCACACTCTCACACATGTGCACACA A T RF00017-4487,RF00017-1020 RNACentral:URS000095255B,RNACentral:URS000099BA6B SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:129832412..129832559 26863196 MeRIP-seq:(Medium) rs1336068924 Functional Loss SNV dbSNP153 33..33 33 - - - 65164 RMVar_ID_65164 Human_SNP_ID_339938367 m1A Human chr7 - 129869250 129869250 129869250 AAGTGGAATGGAATAGAAGGTCACTGAGGAGAAGCTTAAGAAACAAGCCGGGCACGGTGGCTCAC AAGTGGAATGGAATAGAAGGTCACTGAGGAGAGGCTTAAGAAACAAGCCGGGCACGGTGGCTCAC T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129869248..129869541 26863196 MeRIP-seq:(Medium) rs966586718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16009724,Human_RBP_ID_24189985 RMVar_hsa_circ_248413,RMVar_hsa_circ_296224,RMVar_hsa_circ_357661,RMVar_hsa_circ_272435 65165 RMVar_ID_65165 Human_SNP_ID_339960014 m1A Human chr7 + 129952727 129952727 129952727 GCCGCCGCCCCCCGCACGGGGGAACACCGGGCACTGTCCGGCCGGGTGGGGGTGGGGACCCTGCG GCCGCCGCCCCCCGCACGGGGGAACACCGGGCGCTGTCCGGCCGGGTGGGGGTGGGGACCCTGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:129952676..129952877;chr7:129952676..129952925 26863196 MeRIP-seq:(Medium) rs1195000850 Functional Loss SNV dbSNP153 33..33 33 - - - 65166 RMVar_ID_65166 Human_SNP_ID_339960057 m1A Human chr7 - 129952855 129952855 129952855 CAGAGGGTGAGTGGGGAGCAGGCGAGCGAGCCACAGCAGGCAGGAGGGAGCGTCGCGCGGCGCAG CAGAGGGTGAGTGGGGAGCAGGCGAGCGAGCCGCAGCAGGCAGGAGGGAGCGTCGCGCGGCGCAG T C UBE2H Ensembl:ENSG00000186591 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:129952471..129952975;chr7:129951324..129952975 26863196 MeRIP-seq:(Medium) rs1317856683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794541,Human_RBP_ID_842351,Human_RBP_ID_4955991,Human_RBP_ID_5328641,Human_RBP_ID_8944290,Human_RBP_ID_9337377,Human_RBP_ID_18426093,Human_RBP_ID_26358364,Human_RBP_ID_27842959 65167 RMVar_ID_65167 Human_SNP_ID_339960060 m1A Human chr7 - 129952859 129952859 129952859 CGGTCAGAGGGTGAGTGGGGAGCAGGCGAGCGAGCCACAGCAGGCAGGAGGGAGCGTCGCGCGGC CGGTCAGAGGGTGAGTGGGGAGCAGGCGAGCGGGCCACAGCAGGCAGGAGGGAGCGTCGCGCGGC T C UBE2H Ensembl:ENSG00000186591 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:129952626..129952950 26863196 MeRIP-seq:(Medium) rs867891009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794541,Human_RBP_ID_842351,Human_RBP_ID_4955991,Human_RBP_ID_5328641,Human_RBP_ID_8944290,Human_RBP_ID_9337377,Human_RBP_ID_18426093,Human_RBP_ID_26358364,Human_RBP_ID_27842959 65168 RMVar_ID_65168 Human_SNP_ID_339960091 m1A Human chr7 - 129952927 129952927 129952927 GAGCGAGGCTGGGGTAGGGAGGCCGACTGAGCAGGAGTCGTCCGCTTATAGTGGAGGCTGCTAGG GAGCGAGGCTGGGGTAGGGAGGCCGACTGAGCTGGAGTCGTCCGCTTATAGTGGAGGCTGCTAGG T A UBE2H Ensembl:ENSG00000186591 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:129952467..129952975 26863196 MeRIP-seq:(Medium) rs1415135653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795160,Human_RBP_ID_18426093 65169 RMVar_ID_65169 Human_SNP_ID_339985788 m1A Human chr7 + 130051248 130051246 130051248 CTCACGCGTCCACGCCTCCCTCTTCCGGGGCAATCCCCTCATCTATCAGCTGCCGGATTTTCTGG CTCACGCGTCCACGCCTCCCTCTTCCGGGGC__TCCCCTCATCTATCAGCTGCCGGATTTTCTGG CAA C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:130049124..130051254 32194978 MeRIP-seq:(Medium) rs1162132720 Functional Loss DEL dbSNP153 32..33 33 - - - 65170 RMVar_ID_65170 Human_SNP_ID_339985823 m1A Human chr7 - 130051323 130051323 130051323 CTGTGAGGGACAAGCGTTTGCCGTAGGGGTTGAAAAGAATTGGGGTGCAGTAGTTCGCTCCCCAG CTGTGAGGGACAAGCGTTTGCCGTAGGGGTTGGAAAGAATTGGGGTGCAGTAGTTCGCTCCCCAG T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:130051236..130051324 26863196 MeRIP-seq:(Medium) rs764344845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956678,Human_RBP_ID_18426094 RMVar_hsa_circ_114696,RMVar_hsa_circ_248432 65171 RMVar_ID_65171 Human_SNP_ID_340045468 m1A Human chr7 - 130293250 130293249 130293250 AAATAACCAAATAATAAGTCCAAAAGGAACTTACCCAAAAAATTTTTCTTGGCCACAGATGCTGG AAATAACCAAATAATAAGTCCAAAAGGAACTT_CCCAAAAAATTTTTCTTGGCCACAGATGCTGG GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:130293207..130293273;chr7:130293217..130293311 26863196 MeRIP-seq:(Medium) rs781665659 Functional Loss DEL dbSNP153 33..33 33 - - - 65172 RMVar_ID_65172 Human_SNP_ID_340048592 m1A Human chr7 - 130306038 130306038 130306038 CCATTTGCTTCTCCAATCTGAAAAGGCCCCCCAGCCGACTGGGTCTTAGTAGAGAACCCTCCCAC CCATTTGCTTCTCCAATCTGAAAAGGCCCCCCGGCCGACTGGGTCTTAGTAGAGAACCCTCCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:130305994..130306281 26863196 MeRIP-seq:(Medium) rs533155699 Functional Loss SNV dbSNP153 33..33 33 - - - 65173 RMVar_ID_65173 Human_SNP_ID_340050959 m1A Human chr7 - 130315088 130315088 130315088 CCAATTCCCCCCCTCACACCTAAGTGGAAGGGACCTTACCAGATCATCCTTACTACACCCACGGC CCAATTCCCCCCCTCACACCTAAGTGGAAGGGGCCTTACCAGATCATCCTTACTACACCCACGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:130315086..130315157 26863196 MeRIP-seq:(Medium) rs1180925190 Functional Loss SNV dbSNP153 33..33 33 - - - 65174 RMVar_ID_65174 Human_SNP_ID_340081897 m1A Human chr7 - 130440987 130440987 130440987 GTTAGAGGCAACCCGTGAGGCTAGAACCCCGAACGTGGTCGGTTGGAGAAAATATGTCCCTCCGG GTTAGAGGCAACCCGTGAGGCTAGAACCCCGACCGTGGTCGGTTGGAGAAAATATGTCCCTCCGG T G CEP41 Ensembl:ENSG00000106477 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:130440849..130441006;chr7:130440829..130441022;chr7:130440826..130441033 26863196 MeRIP-seq:(Medium) rs782482205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_923221,Human_Splice_Rec_923241,Human_Splice_Rec_923261,Human_Splice_Rec_923281,Human_Splice_Rec_923351,Human_Splice_Rec_923363,Human_Splice_Rec_923383,Human_Splice_Rec_923387,Human_Splice_Rec_923391,Human_Splice_Rec_923395 65175 RMVar_ID_65175 Human_SNP_ID_340096230 m1A Human chr7 + 130503976 130503976 130503976 TATGGGCCATTGGATCCTGTAAATCCCTATCCAGAGTTTTTGGAGCTGTACAGGTGAGTCTCCCC TATGGGCCATTGGATCCTGTAAATCCCTATCCTGAGTTTTTGGAGCTGTACAGGTGAGTCTCCCC A T MEST Ensembl:ENSG00000106484 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:130502713..130505051 32194978 MeRIP-seq:(Medium) rs782817897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24190573 Human_Splice_Rec_923424,Human_Splice_Rec_923425,Human_Splice_Rec_923444,Human_Splice_Rec_923445,Human_Splice_Rec_923464,Human_Splice_Rec_923465,Human_Splice_Rec_923484,Human_Splice_Rec_923485,Human_Splice_Rec_923524,Human_Splice_Rec_923525,Human_Splice_Rec_923562,Human_Splice_Rec_923563,Human_Splice_Rec_923584,Human_Splice_Rec_923585,Human_Splice_Rec_923606,Human_Splice_Rec_923607,Human_Splice_Rec_923654,Human_Splice_Rec_923655 RMVar_hsa_circ_30799,RMVar_hsa_circ_10565 65176 RMVar_ID_65176 Human_SNP_ID_340135625 m1A Human chr7 + 130668684 130668684 130668684 TCGAATTTTTTAATCATCTTGGACGACTTCCCAGCGCCCAGACCCACCGCAACCGTCCCAGGCGC TCGAATTTTTTAATCATCTTGGACGACTTCCCGGCGCCCAGACCCACCGCAACCGTCCCAGGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:130668624..130668700;chr7:130668609..130668694 26863196 MeRIP-seq:(Medium) rs782172247 Functional Loss SNV dbSNP153 33..33 33 - - - 65177 RMVar_ID_65177 Human_SNP_ID_340192984 m1A Human chr7 + 130901544 130901543 130901544 AAACACACACCCCTCCCCCCAGTTCATCTCTTACCCACTCACACAACGAAGATCCGACTTATCCA AAACACACACCCCTCCCCCCAGTTCATCTCTT_CCCACTCACACAACGAAGATCCGACTTATCCA TA T LINC00513 Ensembl:ENSG00000233559 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:130901311..130901559 26863196 MeRIP-seq:(Medium) rs782731708 Functional Loss DEL dbSNP153 33..33 33 - - - 65178 RMVar_ID_65178 Human_SNP_ID_340201358 m1A Human chr7 + 130936782 130936782 130936782 CCTTAGTGGTTTACACACATCATTGCCCAGCAACTACAAATCGATTCCTGCCCACTCTGCACCCC CCTTAGTGGTTTACACACATCATTGCCCAGCAGCTACAAATCGATTCCTGCCCACTCTGCACCCC A G AC058791.1 Ensembl:ENSG00000273319 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:130936536..130936863 26863196 MeRIP-seq:(Medium) rs1256844410 Functional Loss SNV dbSNP153 33..33 33 - - - 65179 RMVar_ID_65179 Human_SNP_ID_340220001 m1A Human chr7 + 131018415 131018415 131018415 TACCCACCTGGACCACCCCGCTCACTTGGGCCACACCACACTTCCACTCTTGTCCCCAGCACACT TACCCACCTGGACCACCCCGCTCACTTGGGCCGCACCACACTTCCACTCTTGTCCCCAGCACACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131018189..131018467 26863196 MeRIP-seq:(Medium) rs900401752 Functional Loss SNV dbSNP153 33..33 33 - - - 65180 RMVar_ID_65180 Human_SNP_ID_340220007 m1A Human chr7 - 131018435 131018435 131018435 GATGCTATGGGGGCAGCGGGAGTGTGCTGGGGACAAGAGTGGAAGTGTGGTGTGGCCCAAGTGAG GATGCTATGGGGGCAGCGGGAGTGTGCTGGGGGCAAGAGTGGAAGTGTGGTGTGGCCCAAGTGAG T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:131018268..131018453 26863196 MeRIP-seq:(Medium) rs995193695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_293175,RMVar_hsa_circ_324639,RMVar_hsa_circ_72221,RMVar_hsa_circ_329083,RMVar_hsa_circ_248504 65181 RMVar_ID_65181 Human_SNP_ID_340227658 m1A Human chr7 + 131049306 131049306 131049306 CCCCCTATCTCAGCAAAGGCACCTCCACTCTCAGTTGTTCAGGCTGCAAACTGTGGAGTCTTCCC CCCCCTATCTCAGCAAAGGCACCTCCACTCTCCGTTGTTCAGGCTGCAAACTGTGGAGTCTTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131049295..131049470 26863196 MeRIP-seq:(Medium) rs1248083082 Functional Loss SNV dbSNP153 33..33 33 - - - 65182 RMVar_ID_65182 Human_SNP_ID_340241538 m1A Human chr7 + 131105734 131105734 131105734 ACAAACCTAGCACTGCTCGCCGAGAAGCGCCAAGCCCCTCAGCCAGCGCCGGGGCACCCGCGCGG ACAAACCTAGCACTGCTCGCCGAGAAGCGCCATGCCCCTCAGCCAGCGCCGGGGCACCCGCGCGG A T lnc-MKLN1-1 RNACentral:URS00008B2E8C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131105687..131105864 26863196 MeRIP-seq:(Medium) rs1175883567 Functional Loss SNV dbSNP153 33..33 33 - - - 65183 RMVar_ID_65183 Human_SNP_ID_340241574 m1A Human chr7 - 131105824 131105824 131105824 GCGGGAGGCGAGGGCGCGGTGACACGGGCCGGAGGGGCCTGCGCCCGCGGAGGGCGCGCGAGGGG GCGGGAGGCGAGGGCGCGGTGACACGGGCCGGTGGGGCCTGCGCCCGCGGAGGGCGCGCGAGGGG T A LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131105790..131105856 26863196 MeRIP-seq:(Medium) rs1253143113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860754,Human_RBP_ID_5220235,Human_RBP_ID_5328644,Human_RBP_ID_5624700,Human_RBP_ID_8220738,Human_RBP_ID_8730556,Human_RBP_ID_17168380,Human_RBP_ID_17427143,Human_RBP_ID_21992568,Human_RBP_ID_22730312,Human_RBP_ID_26793670 RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 65184 RMVar_ID_65184 Human_SNP_ID_340242708 m1A Human chr7 - 131109787 131109787 131109787 GCTTGGCAGCAGAAGGGATGGGACCAGAGAGAAGGGTGTGGAGGAGACCCCAGTGAGGGCCAGGA GCTTGGCAGCAGAAGGGATGGGACCAGAGAGATGGGTGTGGAGGAGACCCCAGTGAGGGCCAGGA T A LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131109646..131109977 26863196 MeRIP-seq:(Medium) rs1248569435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624710,Human_RBP_ID_19135471 Human_Splice_Rec_923833,Human_Splice_Rec_923847,Human_Splice_Rec_923861,Human_Splice_Rec_923881,Human_Splice_Rec_923893,Human_Splice_Rec_923999 65185 RMVar_ID_65185 Human_SNP_ID_340294656 m1A Human chr7 + 131327952 131327952 131327952 CGCTGCGGCGCCCGAGTGCCGGCTTCTCCCCTACGCGCTACACAAGTGGAGCTCCTTTTCCTCCA CGCTGCGGCGCCCGAGTGCCGGCTTCTCCCCTTCGCGCTACACAAGTGGAGCTCCTTTTCCTCCA A T MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:131327903..131327997;chr7:131327904..131328024 26863196 MeRIP-seq:(Medium) rs1322123873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1219892,Human_RBP_ID_4956683,Human_RBP_ID_18876038 Human_Splice_Rec_924191,Human_Splice_Rec_924199,Human_Splice_Rec_924207,Human_Splice_Rec_924239,Human_Splice_Rec_924269 RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248515,RMVar_hsa_circ_81806,RMVar_hsa_circ_126807,RMVar_hsa_circ_248513,RMVar_hsa_circ_110362,RMVar_hsa_circ_248516,RMVar_hsa_circ_248514 65186 RMVar_ID_65186 Human_SNP_ID_340294661 m1A Human chr7 + 131327964 131327964 131327964 CGAGTGCCGGCTTCTCCCCTACGCGCTACACAAGTGGAGCTCCTTTTCCTCCACCTACCTTCCCG CGAGTGCCGGCTTCTCCCCTACGCGCTACACAGGTGGAGCTCCTTTTCCTCCACCTACCTTCCCG A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr7:131327926..131328079;chr7:131327914..131327997 26863196 MeRIP-seq:(Medium) rs765728434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1397453,Human_RBP_ID_4925205,Human_RBP_ID_17311592,Human_RBP_ID_18876038,Human_RBP_ID_23297745 Human_Splice_Rec_924191,Human_Splice_Rec_924199,Human_Splice_Rec_924207,Human_Splice_Rec_924239,Human_Splice_Rec_924269 RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248515,RMVar_hsa_circ_81806,RMVar_hsa_circ_126807,RMVar_hsa_circ_248513,RMVar_hsa_circ_110362,RMVar_hsa_circ_248516,RMVar_hsa_circ_248514 65187 RMVar_ID_65187 Human_SNP_ID_340335808 m1A Human chr7 + 131503551 131503551 131503551 CTGCACGCAGGTCCCCTAAGCAGACCTGGTTCACGCACGGAGACCTGTGTGGGTTAAGCCCCCAT CTGCACGCAGGTCCCCTAAGCAGACCTGGTTCGCGCACGGAGACCTGTGTGGGTTAAGCCCCCAT A G RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:131503501..131503550 32194978 MeRIP-seq:(Medium) rs1361825983 Functional Loss SNV dbSNP153 33..33 33 - - - 65188 RMVar_ID_65188 Human_SNP_ID_340337624 m1A Human chr7 - 131509557 131509557 131509557 ACAGCGTCATCGGTTATCTCGCAAAGAACTCAACAGACCTCCAGTCAGATGCCAGCCAGCTCTAC ACAGCGTCATCGGTTATCTCGCAAAGAACTCAGCAGACCTCCAGTCAGATGCCAGCCAGCTCTAC T C PODXL Ensembl:ENSG00000128567 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:131509436..131509661 26863196 MeRIP-seq:(Medium) rs1355080906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_924440,Human_Splice_Rec_924454,Human_Splice_Rec_924470,Human_Splice_Rec_924492 RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_296567,RMVar_hsa_circ_98583,RMVar_hsa_circ_248565,RMVar_hsa_circ_344425,RMVar_hsa_circ_376614,RMVar_hsa_circ_290464,RMVar_hsa_circ_248567 65189 RMVar_ID_65189 Human_SNP_ID_340338221 m1A Human chr7 - 131511431 131511431 131511431 AACTCCATTCTCTGTTATCTTTACAAACAGCAACCCAGACTACTACGGACTCATCTAACAAAACA AACTCCATTCTCTGTTATCTTTACAAACAGCAGCCCAGACTACTACGGACTCATCTAACAAAACA T C PODXL Ensembl:ENSG00000128567 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr7:131511426..131511450;chr7:131511294..131511450 26863196 MeRIP-seq:(Medium) rs1280652875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_924438,Human_Splice_Rec_924450,Human_Splice_Rec_924468,Human_Splice_Rec_924496 RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_296567,RMVar_hsa_circ_98583,RMVar_hsa_circ_248565,RMVar_hsa_circ_376614,RMVar_hsa_circ_290464,RMVar_hsa_circ_248569,RMVar_hsa_circ_248567,RMVar_hsa_circ_321215 65190 RMVar_ID_65190 Human_SNP_ID_340349340 m1A Human chr7 + 131556221 131556221 131556221 CTGCAGCTCGGCCGGGCAGGGGGCACATGGGCACGGTGGGAGTCCCGGCGGAACCCAGGCCGGCC CTGCAGCTCGGCCGGGCAGGGGGCACATGGGCGCGGTGGGAGTCCCGGCGGAACCCAGGCCGGCC A G RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:131556220..131556600 26863196 MeRIP-seq:(Medium) rs1467898837 Functional Loss SNV dbSNP153 33..33 33 - - - 65191 RMVar_ID_65191 Human_SNP_ID_340349466 m1A Human chr7 - 131556398 131556398 131556398 CTACCGCCCGGACGCGCGGATCCTCCGCCGGCACCGCAGCCACCTGCTCCCGGCCCAGAGGCGAC CTACCGCCCGGACGCGCGGATCCTCCGCCGGCTCCGCAGCCACCTGCTCCCGGCCCAGAGGCGAC T A PODXL Ensembl:ENSG00000128567 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:131556351..131556600 26863196 MeRIP-seq:(Medium) rs1485270807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_98583,RMVar_hsa_circ_376614 65192 RMVar_ID_65192 Human_SNP_ID_340349472 m1A Human chr7 - 131556411 131556411 131556411 GGCGCCCACGCTCCTACCGCCCGGACGCGCGGATCCTCCGCCGGCACCGCAGCCACCTGCTCCCG GGCGCCCACGCTCCTACCGCCCGGACGCGCGGGTCCTCCGCCGGCACCGCAGCCACCTGCTCCCG T C PODXL Ensembl:ENSG00000128567 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131556309..131556625 26863196 MeRIP-seq:(Medium) rs1268784357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26543743 RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_98583,RMVar_hsa_circ_376614 65193 RMVar_ID_65193 Human_SNP_ID_340357661 m1A Human chr7 + 131587175 131587171 131587175 GTGTGTGTGATGAGTGTGGTGTGTGTAGTGTAAGTATGTGGTGCAGCATATATATGTGTGGTGTG GTGTGTGTGATGAGTGTGGTGTGTGTAGT____GTATGTGGTGCAGCATATATATGTGTGGTGTG TGTAA T RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:131587096..131587223 26863196 MeRIP-seq:(Medium) rs984059033 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_248571,RMVar_hsa_circ_248570 65194 RMVar_ID_65194 Human_SNP_ID_340375715 m1A Human chr7 - 131654086 131654086 131654086 TACCACTACAACACATACCACAACACACACACATCACACCACACACACAACACACAGCATACACA TACCACTACAACACATACCACAACACACACACGTCACACCACACACACAACACACAGCATACACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131653926..131654229 26863196 MeRIP-seq:(Medium) rs1381966998 Functional Loss SNV dbSNP153 33..33 33 - - - 65195 RMVar_ID_65195 Human_SNP_ID_340375718 m1A Human chr7 - 131654111 131654097 131654112 CACAAATACACACCCCCACAACACATACCACTACAACACATACCACAACACACACACATCACACC CACAAATACACACCCCCACAACACATACCAC_______________AACACACACACATCACACC TGTGGTATGTGTTGTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131653901..131654138 26863196 MeRIP-seq:(Medium) rs747659829 Functional Loss DEL dbSNP153 32..46 33 - - - 65196 RMVar_ID_65196 Human_SNP_ID_340375727 m1A Human chr7 - 131654111 131654109 131654112 CACAAATACACACCCCCACAACACATACCACTACAACACATACCACAACACACACACATCACACC CACAAATACACACCCCCACAACACATACCAC___AACACATACCACAACACACACACATCACACC TGTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131653901..131654138 26863196 MeRIP-seq:(Medium) rs72544954 Functional Loss DEL dbSNP153 32..34 33 - - - 65197 RMVar_ID_65197 Human_SNP_ID_340375729 m1A Human chr7 - 131654111 131654110 131654112 CACAAATACACACCCCCACAACACATACCACTACAACACATACCACAACACACACACATCACACC CACAAATACACACCCCCACAACACATACCAC__CAACACATACCACAACACACACACATCACACC GTA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131653901..131654138 26863196 MeRIP-seq:(Medium) rs1562942590 Functional Loss DEL dbSNP153 32..33 33 - - - 65198 RMVar_ID_65198 Human_SNP_ID_340375827 m1A Human chr7 - 131654265 131654258 131654265 TCACCACACATACCCACACAACATAACACACAACACACACATCCCTACAACACACACCCACAATA TCACCACACATACCCACACAACATAACACACA_______CATCCCTACAACACACACCCACAATA GTGTGTGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131654215..131654328 26863196 MeRIP-seq:(Medium) rs1245324657 Functional Loss DEL dbSNP153 33..39 33 - - - 65199 RMVar_ID_65199 Human_SNP_ID_340375832 m1A Human chr7 - 131654265 131654265 131654265 TCACCACACATACCCACACAACATAACACACAACACACACATCCCTACAACACACACCCACAATA TCACCACACATACCCACACAACATAACACACACCACACACATCCCTACAACACACACCCACAATA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131654215..131654328 26863196 MeRIP-seq:(Medium) rs13240056 Functional Loss SNV dbSNP153 33..33 33 - - - 65200 RMVar_ID_65200 Human_SNP_ID_340375969 m1A Human chr7 + 131654487 131654478 131654487 TGTATGTGTGGTGTGTGTTATGTGATATGTGCATTGTGTTGTGGGGTGTGTGTCGTAGGGGTGTT TGTATGTGTGGTGTGTGTTATGTG_________TTGTGTTGTGGGGTGTGTGTCGTAGGGGTGTT GATATGTGCA G RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:131654435..131654630 26863196 MeRIP-seq:(Medium) rs1223743776 Functional Loss DEL dbSNP153 25..33 33 - - - 65201 RMVar_ID_65201 Human_SNP_ID_340667534 m1A Human chr7 + 132796467 132796467 132796467 CACCTACCTGTTTGGCATGATTGACACAGTGCATATACTGGGTGGCCAGAGCGGAGCATTTGAGG CACCTACCTGTTTGGCATGATTGACACAGTGCGTATACTGGGTGGCCAGAGCGGAGCATTTGAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:132785562..132796493 32194978 MeRIP-seq:(Medium) rs762036363 Functional Loss SNV dbSNP153 33..33 33 - - - 65202 RMVar_ID_65202 Human_SNP_ID_340676735 m1A Human chr7 - 132838469 132838460 132838469 GTGAAACCTTTGCTATCAATCTTTGTCCACAGAGCTCAGAGTTCTACAGAGTCACCACTGAACAA GTGAAACCTTTGCTATCAATCTTTGTCCACAG_________TTCTACAGAGTCACCACTGAACAA ACTCTGAGCT A CHCHD3 Ensembl:ENSG00000106554 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:132838456..132838523 26863196 MeRIP-seq:(Medium) rs1233019395 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_9403896,Human_RBP_ID_18108617,Human_RBP_ID_26830808 Human_Splice_Rec_924690,Human_Splice_Rec_924691,Human_Splice_Rec_924706,Human_Splice_Rec_924707,Human_Splice_Rec_924718,Human_Splice_Rec_924719,Human_Splice_Rec_924734,Human_Splice_Rec_924735 RMVar_hsa_circ_28109,RMVar_hsa_circ_79252,RMVar_hsa_circ_248605,RMVar_hsa_circ_325510,RMVar_hsa_circ_248606 65203 RMVar_ID_65203 Human_SNP_ID_340683407 m1A Human chr7 - 132868867 132868858 132868867 GGGTCACCAGGCTGTGGTGGGCAAGAGCAAGGAGCCCTGGGGAAAGTCGCACAGCAGTTACTCTC GGGTCACCAGGCTGTGGTGGGCAAGAGCAAGG_________GAAAGTCGCACAGCAGTTACTCTC CCCCAGGGCT C CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:132868864..132868929 26863196 MeRIP-seq:(Medium) rs898554272 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_325510 65204 RMVar_ID_65204 Human_SNP_ID_340683410 m1A Human chr7 - 132868867 132868867 132868867 GGGTCACCAGGCTGTGGTGGGCAAGAGCAAGGAGCCCTGGGGAAAGTCGCACAGCAGTTACTCTC GGGTCACCAGGCTGTGGTGGGCAAGAGCAAGGTGCCCTGGGGAAAGTCGCACAGCAGTTACTCTC T A CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:132868864..132868929 26863196 MeRIP-seq:(Medium) rs1355535837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325510 65205 RMVar_ID_65205 Human_SNP_ID_340687183 m1A Human chr7 + 132885681 132885681 132885681 AAAATAGTCATACCCTCTCCTCCAGTCTAGCCAGCTGTTCTTTGTAGAATGCATCCTGCTTCTTT AAAATAGTCATACCCTCTCCTCCAGTCTAGCCTGCTGTTCTTTGTAGAATGCATCCTGCTTCTTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:132885676..132885750 26863196 MeRIP-seq:(Medium) rs1383344729 Functional Loss SNV dbSNP153 33..33 33 - - - 65206 RMVar_ID_65206 Human_SNP_ID_340687187 m1A Human chr7 - 132885690 132885690 132885690 CCGAGTGCTAAAGAAGCAGGATGCATTCTACAAAGAACAGCTGGCTAGACTGGAGGAGAGGGTAT CCGAGTGCTAAAGAAGCAGGATGCATTCTACACAGAACAGCTGGCTAGACTGGAGGAGAGGGTAT T G CHCHD3 Ensembl:ENSG00000106554 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:132885651..132885725 26863196 MeRIP-seq:(Medium) rs1214010308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9403897,Human_RBP_ID_26830809 Human_Splice_Rec_924688,Human_Splice_Rec_924689,Human_Splice_Rec_924704,Human_Splice_Rec_924705,Human_Splice_Rec_924716,Human_Splice_Rec_924717,Human_Splice_Rec_924732,Human_Splice_Rec_924733 RMVar_hsa_circ_57563,RMVar_hsa_circ_325510,RMVar_hsa_circ_362372,RMVar_hsa_circ_50703 65207 RMVar_ID_65207 Human_SNP_ID_340709416 m1A Human chr7 + 132983999 132983999 132983999 CTCCTCTCCCTCTCCCTCCTCTCCCTCTCCCCACGGTCTCCCTCTCCCCACGGTCTCCCTCTCCC CTCCTCTCCCTCTCCCTCCTCTCCCTCTCCCCCCGGTCTCCCTCTCCCCACGGTCTCCCTCTCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:132983997..132984080 26863196 MeRIP-seq:(Medium) rs1402112564 Functional Loss SNV dbSNP153 33..33 33 - - - 65208 RMVar_ID_65208 Human_SNP_ID_340719003 m1A Human chr7 - 133024496 133024496 133024496 AGAGAGAGGTTTTGGTGGGTTTTGTCATATTTACCAGTATTTTTAGAGAAGAATGATTGTGATAA AGAGAGAGGTTTTGGTGGGTTTTGTCATATTTGCCAGTATTTTTAGAGAAGAATGATTGTGATAA T C CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:133024492..133024600 26863196 MeRIP-seq:(Medium) rs571740271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17637079,Human_RBP_ID_19138414,Human_RBP_ID_22367068 RMVar_hsa_circ_362372,RMVar_hsa_circ_35884,RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_290100,RMVar_hsa_circ_300564,RMVar_hsa_circ_248608 65209 RMVar_ID_65209 Human_SNP_ID_340721475 m1A Human chr7 - 133034787 133034787 133034787 AGCAGCTCCATTTCTGGAGTCTGGGTCTTCCGAGGCCAGGAGCTTGCCTTTCCGCTGAGTCCAGA AGCAGCTCCATTTCTGGAGTCTGGGTCTTCCGCGGCCAGGAGCTTGCCTTTCCGCTGAGTCCAGA T G CHCHD3,AC008038.1 Ensembl:ENSG00000106554,Ensembl:ENSG00000283041 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1562944223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675451,Human_RBP_ID_5104915,Human_RBP_ID_5624220,Human_RBP_ID_9217689,Human_RBP_ID_9337385,Human_RBP_ID_17667975,Human_RBP_ID_18109401,Human_RBP_ID_18174264,Human_RBP_ID_18196107,Human_RBP_ID_18541036,Human_RBP_ID_24191539 RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_300564,RMVar_hsa_circ_341277 65210 RMVar_ID_65210 Human_SNP_ID_340721794 m1A Human chr7 - 133035836 133035836 133035836 CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGATCCGCGTGCTCTCCGCACCACCCCACTTCCAT CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGTTCCGCGTGCTCTCCGCACCACCCCACTTCCAT T A CHCHD3,AC008038.1 Ensembl:ENSG00000106554,Ensembl:ENSG00000283041 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12674366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9217693 Human_miRNA_ID_1855106,Human_miRNA_ID_1856247 RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_300564,RMVar_hsa_circ_341277 65211 RMVar_ID_65211 Human_SNP_ID_340721795 m1A Human chr7 - 133035836 133035836 133035836 CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGATCCGCGTGCTCTCCGCACCACCCCACTTCCAT CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGGTCCGCGTGCTCTCCGCACCACCCCACTTCCAT T C CHCHD3,AC008038.1 Ensembl:ENSG00000106554,Ensembl:ENSG00000283041 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12674366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9217693 Human_miRNA_ID_1855106,Human_miRNA_ID_1856247 RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_300564,RMVar_hsa_circ_341277 65212 RMVar_ID_65212 Human_SNP_ID_340731671 m1A Human chr7 - 133082013 133082013 133082013 CCGCTGTGCGGGAAAAGAATCCAGGCCCTTCCACGCGCGTGTGGGTGCGGGGGCCCCGAAGTGCT CCGCTGTGCGGGAAAAGAATCCAGGCCCTTCCGCGCGCGTGTGGGTGCGGGGGCCCCGAAGTGCT T C CHCHD3 Ensembl:ENSG00000106554 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:133081881..133082050 26863196 MeRIP-seq:(Medium) rs1429252316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86937,Human_RBP_ID_675474,Human_RBP_ID_4955993,Human_RBP_ID_9337387,Human_RBP_ID_9403900,Human_RBP_ID_18426098,Human_RBP_ID_22112014,Human_RBP_ID_27105307 RMVar_hsa_circ_266427 65213 RMVar_ID_65213 Human_SNP_ID_340731675 m1A Human chr7 + 133082026 133082026 133082026 CCCCGCACCCACACGCGCGTGGAAGGGCCTGGATTCTTTTCCCGCACAGCGGGAGCAAGGCCACG CCCCGCACCCACACGCGCGTGGAAGGGCCTGGCTTCTTTTCCCGCACAGCGGGAGCAAGGCCACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:133081926..133082100 26863196 MeRIP-seq:(Medium) rs144858502 Functional Loss SNV dbSNP153 33..33 33 - - - 65214 RMVar_ID_65214 Human_SNP_ID_340731676 m1A Human chr7 + 133082026 133082026 133082026 CCCCGCACCCACACGCGCGTGGAAGGGCCTGGATTCTTTTCCCGCACAGCGGGAGCAAGGCCACG CCCCGCACCCACACGCGCGTGGAAGGGCCTGGTTTCTTTTCCCGCACAGCGGGAGCAAGGCCACG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:133081926..133082100 26863196 MeRIP-seq:(Medium) rs144858502 Functional Loss SNV dbSNP153 33..33 33 - - - 65215 RMVar_ID_65215 Human_SNP_ID_340773896 m1A Human chr7 - 133253175 133253175 133253175 CTGCCTCCTGCCTCCCTCACCTGATCACAGAGATGAGCAGCCCCGAGGGGTCTTTGCTTTTGCTG CTGCCTCCTGCCTCCCTCACCTGATCACAGAGGTGAGCAGCCCCGAGGGGTCTTTGCTTTTGCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:133253125..133253225 26863196 MeRIP-seq:(Medium) rs1449389802 Functional Loss SNV dbSNP153 33..33 33 - - - 65216 RMVar_ID_65216 Human_SNP_ID_340773898 m1A Human chr7 - 133253189 133253189 133253189 CCAGTCCCCAGACCCTGCCTCCTGCCTCCCTCACCTGATCACAGAGATGAGCAGCCCCGAGGGGT CCAGTCCCCAGACCCTGCCTCCTGCCTCCCTCGCCTGATCACAGAGATGAGCAGCCCCGAGGGGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:133253140..133253247 26863196 MeRIP-seq:(Medium) rs1377402906 Functional Loss SNV dbSNP153 33..33 33 - - - 65217 RMVar_ID_65217 Human_SNP_ID_340810314 m1A Human chr7 - 133408074 133408074 133408074 GGCTACCGTCGCCACCACCATCATCATCTATTACACCATCAACACCTCCAACATCACCACTAACT GGCTACCGTCGCCACCACCATCATCATCTATTGCACCATCAACACCTCCAACATCACCACTAACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:133408023..133408125 26863196 MeRIP-seq:(Medium) rs1304366657 Functional Loss SNV dbSNP153 33..33 33 - - - 65218 RMVar_ID_65218 Human_SNP_ID_340826062 m1A Human chr7 + 133475473 133475473 133475473 GAAACCTCAAAGGCCAAAAAATTCTCTTTTCAAGTAAGTATTATTCTGCTGTTAATAGGTTTTAA GAAACCTCAAAGGCCAAAAAATTCTCTTTTCAGGTAAGTATTATTCTGCTGTTAATAGGTTTTAA A G EXOC4 Ensembl:ENSG00000131558 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:133475428..133478969 32194978 MeRIP-seq:(Medium) rs778843137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952806,Human_RBP_ID_3971450,Human_RBP_ID_19021493,Human_RBP_ID_22111243 Human_Splice_Rec_924771,Human_Splice_Rec_924789,Human_Splice_Rec_924807,Human_Splice_Rec_924841,Human_Splice_Rec_924855,Human_Splice_Rec_924859 RMVar_hsa_circ_5925,RMVar_hsa_circ_58905,RMVar_hsa_circ_342842,RMVar_hsa_circ_324917,RMVar_hsa_circ_358198,RMVar_hsa_circ_295146,RMVar_hsa_circ_288008,RMVar_hsa_circ_248622,RMVar_hsa_circ_16444,RMVar_hsa_circ_344009,RMVar_hsa_circ_33522,RMVar_hsa_circ_355658,RMVar_hsa_circ_343374,RMVar_hsa_circ_248628,RMVar_hsa_circ_348306,RMVar_hsa_circ_248629,RMVar_hsa_circ_367446,RMVar_hsa_circ_280833,RMVar_hsa_circ_248630 65219 RMVar_ID_65219 Human_SNP_ID_340868545 m1A Human chr7 + 133652568 133652568 133652568 AAAGGGAAGCCATATAAAGAAGAAAGACAAAGACAGACCAGGGTACAAAGAGGAGTAGTGGGGAA AAAGGGAAGCCATATAAAGAAGAAAGACAAAGGCAGACCAGGGTACAAAGAGGAGTAGTGGGGAA A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:133652554..133652637 26863196 MeRIP-seq:(Medium) rs753867347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16444,RMVar_hsa_circ_343374,RMVar_hsa_circ_367446,RMVar_hsa_circ_248632,RMVar_hsa_circ_354739,RMVar_hsa_circ_357380,RMVar_hsa_circ_271908 65220 RMVar_ID_65220 Human_SNP_ID_340968101 m1A Human chr7 + 134065628 134065628 134065628 GGGCCACATCTTGAAAACTCGTGGAAAGGGAAAGGGGAGGAGATGGGACTTTGACCACACACAGT GGGCCACATCTTGAAAACTCGTGGAAAGGGAAGGGGGAGGAGATGGGACTTTGACCACACACAGT A G EXOC4 Ensembl:ENSG00000131558 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134065579..134065714 26863196 MeRIP-seq:(Medium) rs1249862172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7699400 RMVar_hsa_circ_248638,RMVar_hsa_circ_111333 65221 RMVar_ID_65221 Human_SNP_ID_341026548 m1A Human chr7 - 134316839 134316839 134316839 GCGGCTTTCCAGGACGGTGCGATGTGCTGCGCAGCGAAGAGGCAGGAGGCCGGCTTCCTGGGGTA GCGGCTTTCCAGGACGGTGCGATGTGCTGCGCTGCGAAGAGGCAGGAGGCCGGCTTCCTGGGGTA T A SLC35B4 Ensembl:ENSG00000205060 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:134316752..134316956 26863196 MeRIP-seq:(Medium) rs1050076498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4957469 65222 RMVar_ID_65222 Human_SNP_ID_341058166 m1A Human chr7 - 134449036 134449036 134449036 AACTTCAACCATCTCCAGGTGGAGATGATCTTAAACAAACCTGGCTTGAAGTATAAGCCTGCAGT AACTTCAACCATCTCCAGGTGGAGATGATCTTGAACAAACCTGGCTTGAAGTATAAGCCTGCAGT T C AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134448426..134449138 32194978 MeRIP-seq:(Medium) rs1314335293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675686,Human_RBP_ID_1681938,Human_RBP_ID_18093041,Human_RBP_ID_26543863,Human_RBP_ID_27105382,Human_RBP_ID_27352019 Human_Splice_Rec_925160,Human_Splice_Rec_925161,Human_Splice_Rec_925178,Human_Splice_Rec_925179,Human_Splice_Rec_925196,Human_Splice_Rec_925197,Human_Splice_Rec_925214,Human_Splice_Rec_925215,Human_Splice_Rec_925219,Human_Splice_Rec_925230,Human_Splice_Rec_925238,Human_Splice_Rec_925252 Human_miRNA_ID_2742442 RMVar_hsa_circ_100050,RMVar_hsa_circ_116330,RMVar_hsa_circ_92712,RMVar_hsa_circ_87540,RMVar_hsa_circ_248661,RMVar_hsa_circ_77253,RMVar_hsa_circ_248662,RMVar_hsa_circ_248659,RMVar_hsa_circ_248660,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_24967 65223 RMVar_ID_65223 Human_SNP_ID_341058475 m1A Human chr7 + 134449703 134449703 134449703 GAAGAGGGAACCAGTCACGAAAACAAGGTCCAACCAGGGGCTGTCTTACCGCCCACGTGTCCAGA GAAGAGGGAACCAGTCACGAAAACAAGGTCCACCCAGGGGCTGTCTTACCGCCCACGTGTCCAGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134449701..134449775 32194978 MeRIP-seq:(Medium) rs1442962803 Functional Loss SNV dbSNP153 33..33 33 - - - 65224 RMVar_ID_65224 Human_SNP_ID_341058798 m1A Human chr7 - 134450869 134450869 134450869 TGTGGTGCACGTACCATGAGAAGGGCCTGGTGAAAGGAGCCTGCCAGAAGACACTCAGCGACCTG TGTGGTGCACGTACCATGAGAAGGGCCTGGTGGAAGGAGCCTGCCAGAAGACACTCAGCGACCTG T C AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134450818..134450917 32194978 MeRIP-seq:(Medium) rs2229542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842737,Human_RBP_ID_2035722,Human_RBP_ID_9403912 Human_Splice_Rec_925156,Human_Splice_Rec_925157,Human_Splice_Rec_925174,Human_Splice_Rec_925175,Human_Splice_Rec_925192,Human_Splice_Rec_925193,Human_Splice_Rec_925210,Human_Splice_Rec_925211,Human_Splice_Rec_925226,Human_Splice_Rec_925227,Human_Splice_Rec_925234,Human_Splice_Rec_925235,Human_Splice_Rec_925242,Human_Splice_Rec_925243,Human_Splice_Rec_925248,Human_Splice_Rec_925249,Human_Splice_Rec_925256,Human_Splice_Rec_925257,Human_Splice_Rec_925262,Human_Splice_Rec_925263,Human_Splice_Rec_925268,Human_Splice_Rec_925269 GWAS_ID_7894,GWAS_ID_7895,GWAS_ID_7896,GWAS_ID_7897 RMVar_hsa_circ_100050,RMVar_hsa_circ_87540,RMVar_hsa_circ_77253,RMVar_hsa_circ_248659,RMVar_hsa_circ_248660,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_24967,RMVar_hsa_circ_98357,RMVar_hsa_circ_339781,RMVar_hsa_circ_248672,RMVar_hsa_circ_248673,RMVar_hsa_circ_17467 65225 RMVar_ID_65225 Human_SNP_ID_341058801 m1A Human chr7 - 134450886 134450886 134450886 CCTCTCGCTGGCTTAGCTGTGGTGCACGTACCATGAGAAGGGCCTGGTGAAAGGAGCCTGCCAGA CCTCTCGCTGGCTTAGCTGTGGTGCACGTACCGTGAGAAGGGCCTGGTGAAAGGAGCCTGCCAGA T C AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134450836..134450942 26863196 MeRIP-seq:(Medium) rs780206909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4925848,Human_RBP_ID_9403912 Human_Splice_Rec_925156,Human_Splice_Rec_925174,Human_Splice_Rec_925192,Human_Splice_Rec_925210,Human_Splice_Rec_925226,Human_Splice_Rec_925234,Human_Splice_Rec_925242,Human_Splice_Rec_925248,Human_Splice_Rec_925256,Human_Splice_Rec_925262,Human_Splice_Rec_925268 RMVar_hsa_circ_100050,RMVar_hsa_circ_87540,RMVar_hsa_circ_77253,RMVar_hsa_circ_248659,RMVar_hsa_circ_248660,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_24967,RMVar_hsa_circ_98357,RMVar_hsa_circ_339781,RMVar_hsa_circ_248672,RMVar_hsa_circ_248673,RMVar_hsa_circ_17467 65226 RMVar_ID_65226 Human_SNP_ID_341059076 m1A Human chr7 - 134451689 134451689 134451689 GGTGGCCATTGACGTCGGGTACCGCCACATCGACTGTGCCCATGTGTACCAGAATGAGAATGAGG GGTGGCCATTGACGTCGGGTACCGCCACATCGCCTGTGCCCATGTGTACCAGAATGAGAATGAGG T G AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134451545..134451788 26863196 MeRIP-seq:(Medium) rs1485185263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173941,Human_RBP_ID_675694,Human_RBP_ID_953361,Human_RBP_ID_4925855,Human_RBP_ID_8658806,Human_RBP_ID_17712324,Human_RBP_ID_27105393 Human_Splice_Rec_925154,Human_Splice_Rec_925172,Human_Splice_Rec_925190,Human_Splice_Rec_925224,Human_Splice_Rec_925232,Human_Splice_Rec_925240,Human_Splice_Rec_925246,Human_Splice_Rec_925254,Human_Splice_Rec_925260,Human_Splice_Rec_925266,Human_Splice_Rec_925272 RMVar_hsa_circ_87540,RMVar_hsa_circ_77253,RMVar_hsa_circ_248659,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_24967,RMVar_hsa_circ_98357,RMVar_hsa_circ_339781,RMVar_hsa_circ_248672,RMVar_hsa_circ_248673,RMVar_hsa_circ_4152,RMVar_hsa_circ_17467 65227 RMVar_ID_65227 Human_SNP_ID_341059081 m1A Human chr7 - 134451695 134451695 134451695 CGTGAAGGTGGCCATTGACGTCGGGTACCGCCACATCGACTGTGCCCATGTGTACCAGAATGAGA CGTGAAGGTGGCCATTGACGTCGGGTACCGCCTCATCGACTGTGCCCATGTGTACCAGAATGAGA T A AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:134451645..134451798 26863196 MeRIP-seq:(Medium) rs5056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173941,Human_RBP_ID_675694,Human_RBP_ID_953361,Human_RBP_ID_4925855,Human_RBP_ID_8658806,Human_RBP_ID_17712324,Human_RBP_ID_27105393 Human_Splice_Rec_925154,Human_Splice_Rec_925172,Human_Splice_Rec_925190,Human_Splice_Rec_925224,Human_Splice_Rec_925232,Human_Splice_Rec_925240,Human_Splice_Rec_925246,Human_Splice_Rec_925254,Human_Splice_Rec_925260,Human_Splice_Rec_925266,Human_Splice_Rec_925272 RMVar_hsa_circ_87540,RMVar_hsa_circ_77253,RMVar_hsa_circ_248659,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_24967,RMVar_hsa_circ_98357,RMVar_hsa_circ_339781,RMVar_hsa_circ_248672,RMVar_hsa_circ_248673,RMVar_hsa_circ_4152,RMVar_hsa_circ_17467 65228 RMVar_ID_65228 Human_SNP_ID_341060998 m1A Human chr7 - 134459056 134459056 134459056 GCGGGGGTCTGGGGAGCGCAGCAGCCATGGCAAGCCGTCTCCTGCTCAACAACGGCGCCAAGATG GCGGGGGTCTGGGGAGCGCAGCAGCCATGGCAGGCCGTCTCCTGCTCAACAACGGCGCCAAGATG T C AKR1B1 Ensembl:ENSG00000085662 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:134458934..134459150 26863196 MeRIP-seq:(Medium) rs770560951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83137,Human_RBP_ID_173942,Human_RBP_ID_253056,Human_RBP_ID_675698,Human_RBP_ID_842739,Human_RBP_ID_4925859,Human_RBP_ID_24192598,Human_RBP_ID_27105397 Human_Splice_Rec_925153,Human_Splice_Rec_925171,Human_Splice_Rec_925189,Human_Splice_Rec_925231,Human_Splice_Rec_925253,Human_Splice_Rec_925265,Human_Splice_Rec_925271 RMVar_hsa_circ_87540,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_98357,RMVar_hsa_circ_248673 65229 RMVar_ID_65229 Human_SNP_ID_341061008 m1A Human chr7 - 134459062 134459062 134459062 TACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCATGGCAAGCCGTCTCCTGCTCAACAACGGCGCC TACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCGTGGCAAGCCGTCTCCTGCTCAACAACGGCGCC T C AKR1B1 Ensembl:ENSG00000085662 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134458948..134459150 26863196 MeRIP-seq:(Medium) rs564547015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83137,Human_RBP_ID_173942,Human_RBP_ID_253056,Human_RBP_ID_675698,Human_RBP_ID_842739,Human_RBP_ID_4925859,Human_RBP_ID_7699580,Human_RBP_ID_24192598,Human_RBP_ID_27105397 Human_Splice_Rec_925153,Human_Splice_Rec_925171,Human_Splice_Rec_925189,Human_Splice_Rec_925231,Human_Splice_Rec_925253,Human_Splice_Rec_925265,Human_Splice_Rec_925271 RMVar_hsa_circ_87540,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_98357,RMVar_hsa_circ_248673 65230 RMVar_ID_65230 Human_SNP_ID_341061009 m1A Human chr7 - 134459062 134459062 134459062 TACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCATGGCAAGCCGTCTCCTGCTCAACAACGGCGCC TACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCCTGGCAAGCCGTCTCCTGCTCAACAACGGCGCC T G AKR1B1 Ensembl:ENSG00000085662 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134458948..134459150 26863196 MeRIP-seq:(Medium) rs564547015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83137,Human_RBP_ID_173942,Human_RBP_ID_253056,Human_RBP_ID_675698,Human_RBP_ID_842739,Human_RBP_ID_4925859,Human_RBP_ID_7699580,Human_RBP_ID_24192598,Human_RBP_ID_27105397 Human_Splice_Rec_925153,Human_Splice_Rec_925171,Human_Splice_Rec_925189,Human_Splice_Rec_925231,Human_Splice_Rec_925253,Human_Splice_Rec_925265,Human_Splice_Rec_925271 RMVar_hsa_circ_87540,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_98357,RMVar_hsa_circ_248673 65231 RMVar_ID_65231 Human_SNP_ID_341061023 m1A Human chr7 - 134459069 134459069 134459069 CGCACCGTACTGGGCGGGGGTCTGGGGAGCGCAGCAGCCATGGCAAGCCGTCTCCTGCTCAACAA CGCACCGTACTGGGCGGGGGTCTGGGGAGCGCGGCAGCCATGGCAAGCCGTCTCCTGCTCAACAA T C AKR1B1 Ensembl:ENSG00000085662 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:134458933..134459150 26863196 MeRIP-seq:(Medium) rs767726595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83137,Human_RBP_ID_173942,Human_RBP_ID_253056,Human_RBP_ID_842739,Human_RBP_ID_4925860,Human_RBP_ID_7699580,Human_RBP_ID_8908115,Human_RBP_ID_24192598 Human_Splice_Rec_925153,Human_Splice_Rec_925171,Human_Splice_Rec_925189,Human_Splice_Rec_925231,Human_Splice_Rec_925253,Human_Splice_Rec_925265,Human_Splice_Rec_925271 RMVar_hsa_circ_87540,RMVar_hsa_circ_248658,RMVar_hsa_circ_99117,RMVar_hsa_circ_248669,RMVar_hsa_circ_98357,RMVar_hsa_circ_248673 65232 RMVar_ID_65232 Human_SNP_ID_341108232 m1A Human chr7 - 134646909 134646897 134646909 TCACCTGCAAAGGGGCCACCAGCAGCAGCAGCAGCAGCAGCAGCCGCTCCTCCGAGCCGCCAAAG TCACCTGCAAAGGGGCCACCAGCAGCAGCAGC____________CGCTCCTCCGAGCCGCCAAAG GGCTGCTGCTGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134646859..134646943 26863196 MeRIP-seq:(Medium) rs147174635 Functional Loss DEL dbSNP153 33..44 33 - - - 65233 RMVar_ID_65233 Human_SNP_ID_341108233 m1A Human chr7 - 134646909 134646897 134646909 TCACCTGCAAAGGGGCCACCAGCAGCAGCAGCAGCAGCAGCAGCCGCTCCTCCGAGCCGCCAAAG TCACCTGCAAAGGGGCCACCAGCAGCAGCAGC_________AGCCGCTCCTCCGAGCCGCCAAAG GGCTGCTGCTGCT GGCT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134646859..134646943 26863196 MeRIP-seq:(Medium) rs147174635 Functional Loss DEL dbSNP153 33..41 33 - - - 65234 RMVar_ID_65234 Human_SNP_ID_341108234 m1A Human chr7 - 134646909 134646897 134646909 TCACCTGCAAAGGGGCCACCAGCAGCAGCAGCAGCAGCAGCAGCCGCTCCTCCGAGCCGCCAAAG TCACCTGCAAAGGGGCCACCAGCAGCAGCAGC______AGCAGCCGCTCCTCCGAGCCGCCAAAG GGCTGCTGCTGCT GGCTGCT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134646859..134646943 26863196 MeRIP-seq:(Medium) rs147174635 Functional Loss DEL dbSNP153 33..38 33 - - - 65235 RMVar_ID_65235 Human_SNP_ID_341108235 m1A Human chr7 - 134646909 134646897 134646909 TCACCTGCAAAGGGGCCACCAGCAGCAGCAGCAGCAGCAGCAGCCGCTCCTCCGAGCCGCCAAAG TCACCTGCAAAGGGGCCACCAGCAGCAGCAGC___AGCAGCAGCCGCTCCTCCGAGCCGCCAAAG GGCTGCTGCTGCT GGCTGCTGCT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134646859..134646943 26863196 MeRIP-seq:(Medium) rs147174635 Functional Loss DEL dbSNP153 33..35 33 - - - 65236 RMVar_ID_65236 Human_SNP_ID_341138686 m1A Human chr7 - 134779744 134779744 134779744 TAAAAAAGAAAGCCTTCTGTGCCTTACCTTGTAGTCTGAAACTTCTTCCCGAGGACTAAGTCGGA TAAAAAAGAAAGCCTTCTGTGCCTTACCTTGTGGTCTGAAACTTCTTCCCGAGGACTAAGTCGGA T C lnc-C7orf49-6,lnc-C7orf49-6:2 RNACentral:URS0000D5BCDD,RNACentral:URS0000D5C1B5 lincRNA,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134779651..134809593 32194978 MeRIP-seq:(Medium) rs1479601410 Functional Loss SNV dbSNP153 33..33 33 - - - 65237 RMVar_ID_65237 Human_SNP_ID_341138687 m1A Human chr7 - 134779744 134779744 134779744 TAAAAAAGAAAGCCTTCTGTGCCTTACCTTGTAGTCTGAAACTTCTTCCCGAGGACTAAGTCGGA TAAAAAAGAAAGCCTTCTGTGCCTTACCTTGTCGTCTGAAACTTCTTCCCGAGGACTAAGTCGGA T G lnc-C7orf49-6,lnc-C7orf49-6:2 RNACentral:URS0000D5BCDD,RNACentral:URS0000D5C1B5 lincRNA,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134779651..134809593 32194978 MeRIP-seq:(Medium) rs1479601410 Functional Loss SNV dbSNP153 33..33 33 - - - 65238 RMVar_ID_65238 Human_SNP_ID_341145988 m1A Human chr7 + 134813921 134813920 134813921 GTAAAGGACGGTGGGTGGCTGAGGCATGTGGGAACACAAGATCATTGGAGGACAGAAGCCCAAGG GTAAAGGACGGTGGGTGGCTGAGGCATGTGGG_ACACAAGATCATTGGAGGACAGAAGCCCAAGG GA G CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:134813915..134814065 26863196 MeRIP-seq:(Medium) rs893577574 Functional Loss DEL dbSNP153 33..33 33 - - - 65239 RMVar_ID_65239 Human_SNP_ID_341157696 m1A Human chr7 - 134869112 134869112 134869112 TCTCTGACTAGTTCCATTGCAGGATAATGACTACCTTTCCTTCTCTTGGCATGATTGTTTAGCTC TCTCTGACTAGTTCCATTGCAGGATAATGACTGCCTTTCCTTCTCTTGGCATGATTGTTTAGCTC T C AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:134869110..134869284 26863196 MeRIP-seq:(Medium) rs1251599438 Functional Loss SNV dbSNP153 33..33 33 - - - 65240 RMVar_ID_65240 Human_SNP_ID_341162578 m1A Human chr7 + 134891492 134891492 134891492 ACCAACGTGTTAACACAAAGGGAGAACACGGGAGCATCCTGCACCGTGCATTTCAGCCACAGATC ACCAACGTGTTAACACAAAGGGAGAACACGGGTGCATCCTGCACCGTGCATTTCAGCCACAGATC A T CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:134891476..134899872 26863196 MeRIP-seq:(Medium) rs137987656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176888,Human_RBP_ID_26358672 RMVar_hsa_circ_61892 65241 RMVar_ID_65241 Human_SNP_ID_341170824 m1A Human chr7 + 134928846 134928846 134928846 AGCCCGACAGGAACGGCTGCGGCAGAAGCAGGAGGAAGAATCCTTGGGACAGGTGACCGACCAGG AGCCCGACAGGAACGGCTGCGGCAGAAGCAGGGGGAAGAATCCTTGGGACAGGTGACCGACCAGG A G CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:134928776..134928900 32194978 MeRIP-seq:(Medium) rs754125928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84143,Human_RBP_ID_217433,Human_RBP_ID_253321,Human_RBP_ID_954958,Human_RBP_ID_4960172,Human_RBP_ID_9403917,Human_RBP_ID_21557398,Human_RBP_ID_23080585,Human_RBP_ID_23120514,Human_RBP_ID_26356074 Human_Splice_Rec_925404,Human_Splice_Rec_925405,Human_Splice_Rec_925430,Human_Splice_Rec_925431,Human_Splice_Rec_925450,Human_Splice_Rec_925451,Human_Splice_Rec_925480,Human_Splice_Rec_925490,Human_Splice_Rec_925491,Human_Splice_Rec_925518,Human_Splice_Rec_925519,Human_Splice_Rec_925546,Human_Splice_Rec_925547,Human_Splice_Rec_925566,Human_Splice_Rec_925567,Human_Splice_Rec_925602,Human_Splice_Rec_925603,Human_Splice_Rec_925608,Human_Splice_Rec_925610,Human_Splice_Rec_925611,Human_Splice_Rec_925634,Human_Splice_Rec_925635,Human_Splice_Rec_925658,Human_Splice_Rec_925659,Human_Splice_Rec_925680,Human_Splice_Rec_925681,Human_Splice_Rec_925704,Human_Splice_Rec_925705 Human_miRNA_ID_2875279 RMVar_hsa_circ_61892,RMVar_hsa_circ_248677,RMVar_hsa_circ_369613 65242 RMVar_ID_65242 Human_SNP_ID_341171908 m1A Human chr7 + 134933305 134933305 134933305 CACCAAGTCCTACCAGAAGAATGATTGGAGGGATGCTGAAGAAAACAAGAAAGAAGACAAGGAAA CACCAAGTCCTACCAGAAGAATGATTGGAGGGGTGCTGAAGAAAACAAGAAAGAAGACAAGGAAA A G CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:134933261..134933454 26863196 MeRIP-seq:(Medium) rs1466778281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84147,Human_RBP_ID_954959,Human_RBP_ID_9403922,Human_RBP_ID_21557400,Human_RBP_ID_23080704,Human_RBP_ID_24549155 Human_Splice_Rec_925407,Human_Splice_Rec_925433,Human_Splice_Rec_925453,Human_Splice_Rec_925521,Human_Splice_Rec_925549,Human_Splice_Rec_925569,Human_Splice_Rec_925613,Human_Splice_Rec_925637,Human_Splice_Rec_925661,Human_Splice_Rec_925683 Human_miRNA_ID_2421569 RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_248678 65243 RMVar_ID_65243 Human_SNP_ID_341171939 m1A Human chr7 - 134933387 134933387 134933387 GTTGTTTTCTCTTCCACCATCACCTCTACCTGATTTTCTCCAATGCTCCCTCGCTTTGGCTTCTC GTTGTTTTCTCTTCCACCATCACCTCTACCTGGTTTTCTCCAATGCTCCCTCGCTTTGGCTTCTC T C AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134933261..134933412 32194978 MeRIP-seq:(Medium) rs1415832510 Functional Loss SNV dbSNP153 33..33 33 - - - 65244 RMVar_ID_65244 Human_SNP_ID_341173749 m1A Human chr7 - 134941054 134941054 134941054 CAACAGTACATATCAGGAAGAAACAGAACAAGAAAAATCTTATTAGGTTTTGGTTGGTATCATCA CAACAGTACATATCAGGAAGAAACAGAACAAGCAAAATCTTATTAGGTTTTGGTTGGTATCATCA T G AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134941052..134941267 26863196 MeRIP-seq:(Medium) rs754628720 Functional Loss SNV dbSNP153 33..33 33 - - - 65245 RMVar_ID_65245 Human_SNP_ID_341175332 m1A Human chr7 + 134947701 134947701 134947701 TGGAGGAACTCAAGAAAAAGAGGGAGGAGAGAAGGAAGGTCCTGGAGGAGGAAGAGCAGAGGAGG TGGAGGAACTCAAGAAAAAGAGGGAGGAGAGAGGGAAGGTCCTGGAGGAGGAAGAGCAGAGGAGG A G CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134947651..134947775 32194978 MeRIP-seq:(Medium) rs1385414837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7699702,Human_RBP_ID_9403931,Human_RBP_ID_21557402,Human_RBP_ID_23080707,Human_RBP_ID_23120517,Human_RBP_ID_24549158,Human_RBP_ID_26356079 Human_Splice_Rec_925411,Human_Splice_Rec_925437,Human_Splice_Rec_925459,Human_Splice_Rec_925499,Human_Splice_Rec_925525,Human_Splice_Rec_925553,Human_Splice_Rec_925573,Human_Splice_Rec_925619,Human_Splice_Rec_925641,Human_Splice_Rec_925665,Human_Splice_Rec_925689 RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_248678,RMVar_hsa_circ_356673,RMVar_hsa_circ_326037,RMVar_hsa_circ_281485,RMVar_hsa_circ_35162,RMVar_hsa_circ_248679 65246 RMVar_ID_65246 Human_SNP_ID_341175340 m1A Human chr7 + 134947723 134947723 134947723 GGAGGAGAGAAGGAAGGTCCTGGAGGAGGAAGAGCAGAGGAGGAAGCAGGAGGAAGCCGATCGAA GGAGGAGAGAAGGAAGGTCCTGGAGGAGGAAGCGCAGAGGAGGAAGCAGGAGGAAGCCGATCGAA A C CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:134947494..134947821 26863196 MeRIP-seq:(Medium) rs1264830373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84160,Human_RBP_ID_793312,Human_RBP_ID_843368,Human_RBP_ID_1070208,Human_RBP_ID_3061016,Human_RBP_ID_7699702,Human_RBP_ID_9403931,Human_RBP_ID_21557402,Human_RBP_ID_23080707,Human_RBP_ID_23120517,Human_RBP_ID_24549158,Human_RBP_ID_26356079 Human_Splice_Rec_925411,Human_Splice_Rec_925437,Human_Splice_Rec_925459,Human_Splice_Rec_925499,Human_Splice_Rec_925525,Human_Splice_Rec_925553,Human_Splice_Rec_925573,Human_Splice_Rec_925619,Human_Splice_Rec_925641,Human_Splice_Rec_925665,Human_Splice_Rec_925689 RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_248678,RMVar_hsa_circ_356673,RMVar_hsa_circ_326037,RMVar_hsa_circ_281485,RMVar_hsa_circ_35162,RMVar_hsa_circ_248679 65247 RMVar_ID_65247 Human_SNP_ID_341175886 m1A Human chr7 + 134950313 134950313 134950313 TGCCTCTCCAACTGTGCTCTCTCTCCTACAGCACTCTTCCCTTTGGCTGTGAAGCTGGTACTGAT TGCCTCTCCAACTGTGCTCTCTCTCCTACAGCGCTCTTCCCTTTGGCTGTGAAGCTGGTACTGAT A G CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:134950311..134950525 26863196 MeRIP-seq:(Medium) rs1365112750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_248678,RMVar_hsa_circ_326037,RMVar_hsa_circ_281485,RMVar_hsa_circ_35162,RMVar_hsa_circ_248679 65248 RMVar_ID_65248 Human_SNP_ID_341176450 m1A Human chr7 + 134952961 134952961 134952961 TAATGCATGCTATGTCCTATGAGGGAAAGAACAAAGCAAGGTGGCTGCCCTGATGGCTCTAATGA TAATGCATGCTATGTCCTATGAGGGAAAGAACGAAGCAAGGTGGCTGCCCTGATGGCTCTAATGA A G CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:134950307..134958100 26863196 MeRIP-seq:(Medium) rs1222170339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51204,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_35162,RMVar_hsa_circ_40875 65249 RMVar_ID_65249 Human_SNP_ID_341177576 m1A Human chr7 - 134958054 134958054 134958054 TTCTGCTCGCTCTTCTATCTAGGAATTACAAAAGAAAATAAACCCAATTAATATTTCAAGCTTAT TTCTGCTCGCTCTTCTATCTAGGAATTACAAACGAAAATAAACCCAATTAATATTTCAAGCTTAT T G AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134958051..134958100 26863196 MeRIP-seq:(Medium) rs1190583635 Functional Loss SNV dbSNP153 33..33 33 - - - 65250 RMVar_ID_65250 Human_SNP_ID_341177632 m1A Human chr7 + 134958240 134958240 134958240 GCAGTGGTGTCAAATCGACCCATCAAGCAGCAATAGTCTCCAAGATTGACAGCAGACTGGAGCAG GCAGTGGTGTCAAATCGACCCATCAAGCAGCAGTAGTCTCCAAGATTGACAGCAGACTGGAGCAG A G CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134958094..134960124 32194978 MeRIP-seq:(Medium) rs112633425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9403939,Human_RBP_ID_26356081,Human_RBP_ID_27105433 Human_Splice_Rec_925416,Human_Splice_Rec_925417,Human_Splice_Rec_925442,Human_Splice_Rec_925443,Human_Splice_Rec_925464,Human_Splice_Rec_925465,Human_Splice_Rec_925504,Human_Splice_Rec_925505,Human_Splice_Rec_925530,Human_Splice_Rec_925531,Human_Splice_Rec_925558,Human_Splice_Rec_925559,Human_Splice_Rec_925578,Human_Splice_Rec_925579,Human_Splice_Rec_925624,Human_Splice_Rec_925625,Human_Splice_Rec_925646,Human_Splice_Rec_925647,Human_Splice_Rec_925670,Human_Splice_Rec_925671,Human_Splice_Rec_925694,Human_Splice_Rec_925695,Human_Splice_Rec_925714,Human_Splice_Rec_925715 Human_miRNA_ID_270192 RMVar_hsa_circ_51204,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_35162,RMVar_hsa_circ_16704,RMVar_hsa_circ_361588,RMVar_hsa_circ_40875,RMVar_hsa_circ_56664,RMVar_hsa_circ_27702 65251 RMVar_ID_65251 Human_SNP_ID_341177641 m1A Human chr7 - 134958275 134958275 134958275 CTGAGGACAATTCTCACCTCAATTGCACTGGTATACTGCTCCAGTCTGCTGTCAATCTTGGAGAC CTGAGGACAATTCTCACCTCAATTGCACTGGTGTACTGCTCCAGTCTGCTGTCAATCTTGGAGAC T C AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:134958226..134958275 26863196 MeRIP-seq:(Medium) rs1274136015 Functional Loss SNV dbSNP153 33..33 33 - - - 65252 RMVar_ID_65252 Human_SNP_ID_341179280 m1A Human chr7 - 134965375 134965372 134965376 CTAGTCTTCCCAATAGATTACCTTAGTGGGGGAAGTGACCTTATCCACAGATTGCTTTTCCCAGA CTAGTCTTCCCAATAGATTACCTTAGTGGGG____TGACCTTATCCACAGATTGCTTTTCCCAGA ACTTC A AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:134965327..134968480 32194978 MeRIP-seq:(Medium) rs1300946906 Functional Loss DEL dbSNP153 32..35 33 - - - 65253 RMVar_ID_65253 Human_SNP_ID_341180253 m1A Human chr7 + 134970155 134970155 134970155 CAGAAGTCAAACCCTCATGACAAAGTAGGCACAAGTCTACAATAAGCTAAATCAGAATTTACAAA CAGAAGTCAAACCCTCATGACAAAGTAGGCACTAGTCTACAATAAGCTAAATCAGAATTTACAAA A T CALD1 Ensembl:ENSG00000122786 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:134970041..134970200 26863196 MeRIP-seq:(Medium) rs1269216210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27764226 Human_miRNA_ID_1746989 65254 RMVar_ID_65254 Human_SNP_ID_341184234 m1A Human chr7 - 134986566 134986566 134986566 GCGGAGAACCCGGTATCCAGCCGCTAGAAGTAACGCCACTGCTGGAGATCCGCAGCCCCAGCCAC GCGGAGAACCCGGTATCCAGCCGCTAGAAGTAGCGCCACTGCTGGAGATCCGCAGCCCCAGCCAC T C AC083870.1 Ensembl:ENSG00000286458 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:134986542..134986771 26863196 MeRIP-seq:(Medium) rs1411243589 Functional Loss SNV dbSNP153 33..33 33 - - - 65255 RMVar_ID_65255 Human_SNP_ID_341184313 m1A Human chr7 + 134986756 134986756 134986756 GCCCCCTGCGGGAAGCGAGCGCGCCCCGGAAAATGAGCGCCTCCCCACACCAAGGTGTCCAGGAG GCCCCCTGCGGGAAGCGAGCGCGCCCCGGAAATTGAGCGCCTCCCCACACCAAGGTGTCCAGGAG A T AGBL3 Ensembl:ENSG00000146856 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:134986656..134987930 26863410 MeRIP-seq:(Medium) rs1454975985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5403376 65256 RMVar_ID_65256 Human_SNP_ID_640071877 m1A Human chr18 - 21111663 21111663 21111663 GGACCGCAGCCCCTCCCAGAAGCTCCCCCATCAGCAGCCGCCGGGACCCAACTATCGTCTTCCTC GGACCGCAGCCCCTCCCAGAAGCTCCCCCATCGGCAGCCGCCGGGACCCAACTATCGTCTTCCTC T C ROCK1 Ensembl:ENSG00000067900 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:21111614..21111741 26863196 MeRIP-seq:(Medium) rs1396139913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494159 65257 RMVar_ID_65257 Human_SNP_ID_640100445 m1A Human chr18 - 21242318 21242318 21242318 CTCGGCTCGGCCGGGCTGGTCTCCCCACCCCCAGTGCCGTTCCCTGCGCCGCGCTGCGCTCCGCT CTCGGCTCGGCCGGGCTGGTCTCCCCACCCCCTGTGCCGTTCCCTGCGCCGCGCTGCGCTCCGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:21242277..21242517;chr18:21242276..21242680 26863196 MeRIP-seq:(Medium) rs1339294982 Functional Loss SNV dbSNP153 33..33 33 - - - 65258 RMVar_ID_65258 Human_SNP_ID_640100498 m1A Human chr18 + 21242444 21242444 21242444 TCCGGGGCGCGGGCAGGAGGTGAGAGGTCGCGAACCGGGCGCGGGAGCTCGCCTGTGACCGGCAG TCCGGGGCGCGGGCAGGAGGTGAGAGGTCGCGCACCGGGCGCGGGAGCTCGCCTGTGACCGGCAG A C GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:21242276..21242662 26863196 MeRIP-seq:(Medium) rs1011890692 Functional Loss SNV dbSNP153 33..33 33 - - - 65259 RMVar_ID_65259 Human_SNP_ID_640100636 m1A Human chr18 + 21242880 21242880 21242880 GGGGGTGCCGGGCAGGCGGGCGGGCGACAGGTAGGGCGCCGCGGAGGTGGCGGGGAGAGGATGGA GGGGGTGCCGGGCAGGCGGGCGGGCGACAGGTGGGGCGCCGCGGAGGTGGCGGGGAGAGGATGGA A G GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:21242741..21242946 26863196 MeRIP-seq:(Medium) rs866400568 Functional Loss SNV dbSNP153 33..33 33 - - - 65260 RMVar_ID_65260 Human_SNP_ID_640125876 m1A Human chr18 + 21363271 21363271 21363271 GAAGATACTTGAGAAAGGCTCCCCCTGCCCCCACTCCGCCTCCCCCCCGCCCCCCCCCCCCCACA GAAGATACTTGAGAAAGGCTCCCCCTGCCCCCCCTCCGCCTCCCCCCCGCCCCCCCCCCCCCACA A C GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:21363259..21363391 26863196 MeRIP-seq:(Medium) rs868410355 Functional Loss SNV dbSNP153 33..33 33 - - - 65261 RMVar_ID_65261 Human_SNP_ID_640184513 m1A Human chr18 - 21612414 21612414 21612414 CACCTCACGAGCTTCATCCTAGCGGCGCCGTCACCCTCTGGGTCCGACAGCACACAGAATCCTTC CACCTCACGAGCTTCATCCTAGCGGCGCCGTCTCCCTCTGGGTCCGACAGCACACAGAATCCTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:21612326..21612450 32194978 MeRIP-seq:(Medium) rs200819984 Functional Loss SNV dbSNP153 33..33 33 - - - 65262 RMVar_ID_65262 Human_SNP_ID_640187331 m1A Human chr18 + 21622776 21622776 21622776 CATGAAACTGTAACCATTGAATTGAAGAACGGAACACAGGTCCATGGAACAATCACAGGTACGGA CATGAAACTGTAACCATTGAATTGAAGAACGGCACACAGGTCCATGGAACAATCACAGGTACGGA A C SNRPD1 Ensembl:ENSG00000167088 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:21622673..21622855 26863196 MeRIP-seq:(Medium) rs747559938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906706,Human_RBP_ID_1011534,Human_RBP_ID_1548251,Human_RBP_ID_1873297,Human_RBP_ID_3551398,Human_RBP_ID_4494980,Human_RBP_ID_5115811,Human_RBP_ID_6672155,Human_RBP_ID_8469201,Human_RBP_ID_9379540,Human_RBP_ID_13260312,Human_RBP_ID_17495704,Human_RBP_ID_18440049,Human_RBP_ID_18714740,Human_RBP_ID_23762239,Human_RBP_ID_26334355,Human_RBP_ID_26977774 Human_Splice_Rec_1898528,Human_Splice_Rec_1898529,Human_Splice_Rec_1898534,Human_Splice_Rec_1898535 RMVar_hsa_circ_124957,RMVar_hsa_circ_189007,RMVar_hsa_circ_189006,RMVar_hsa_circ_298700 65263 RMVar_ID_65263 Human_SNP_ID_640202542 m1A Human chr18 - 21681366 21681366 21681366 ATAGTATTAGTCGTATTGTGGGAAGTAAAGACAAGGGAGTCTAGGGTAATGTTTCTAGCTTGGCT ATAGTATTAGTCGTATTGTGGGAAGTAAAGACGAGGGAGTCTAGGGTAATGTTTCTAGCTTGGCT T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:21681269..21681538 26863196 MeRIP-seq:(Medium) rs929210949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13261017 RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_330655,RMVar_hsa_circ_189012 65264 RMVar_ID_65264 Human_SNP_ID_640205817 m1A Human chr18 - 21694816 21694814 21694817 GATCAGCGGTGTCACATACAACTTAAAGGAGAAGGAGGATGAATAAAGCAAAACATGAGAATCTC GATCAGCGGTGTCACATACAACTTAAAGGAG___GAGGATGAATAAAGCAAAACATGAGAATCTC CCTT C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:21694769..21694897 26863196 MeRIP-seq:(Medium) rs1216316429 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13261308 RMVar_hsa_circ_97754,RMVar_hsa_circ_189012 65265 RMVar_ID_65265 Human_SNP_ID_640208611 m1A Human chr18 + 21704738 21704738 21704738 AGCCGGCTGGCGAGCGGGCGAGAGCGGGCGAGAGCGGACGCGGCGCCGCTGCCTACTCCCGACCA AGCCGGCTGGCGAGCGGGCGAGAGCGGGCGAGGGCGGACGCGGCGCCGCTGCCTACTCCCGACCA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr18:21704655..21704755;chr18:21704639..21704766 26863410 MeRIP-seq:(Medium) rs1272756844 Functional Loss SNV dbSNP153 33..33 33 - - - 65266 RMVar_ID_65266 Human_SNP_ID_640208612 m1A Human chr18 + 21704738 21704738 21704738 AGCCGGCTGGCGAGCGGGCGAGAGCGGGCGAGAGCGGACGCGGCGCCGCTGCCTACTCCCGACCA AGCCGGCTGGCGAGCGGGCGAGAGCGGGCGAGTGCGGACGCGGCGCCGCTGCCTACTCCCGACCA A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr18:21704655..21704755;chr18:21704639..21704766 26863410 MeRIP-seq:(Medium) rs1272756844 Functional Loss SNV dbSNP153 33..33 33 - - - 65267 RMVar_ID_65267 Human_SNP_ID_640209447 m1A Human chr18 + 21707638 21707638 21707638 GGAAGAAACTCCAAACACATCCGAAGATCAGAAGGAACCAACTCTGGACGCCCCTCTTTTAAGAA GGAAGAAACTCCAAACACATCCGAAGATCAGAGGGAACCAACTCTGGACGCCCCTCTTTTAAGAA A G MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:21707589..21707801 26863196 MeRIP-seq:(Medium) rs1026819538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82071,RMVar_hsa_circ_102856,RMVar_hsa_circ_189017,RMVar_hsa_circ_189018 65268 RMVar_ID_65268 Human_SNP_ID_640217590 m1A Human chr18 - 21740883 21740883 21740883 TTCTCAGAGTGTCTAGGAGGGGGATCCTCGGCAATAATAGAGTGGGAAGGCTTCCAGAGAGCCGC TTCTCAGAGTGTCTAGGAGGGGGATCCTCGGCCATAATAGAGTGGGAAGGCTTCCAGAGAGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:21740834..21741033 26863196 MeRIP-seq:(Medium) rs1216492519 Functional Loss SNV dbSNP153 33..33 33 - - - 65269 RMVar_ID_65269 Human_SNP_ID_640217624 m1A Human chr18 + 21740957 21740957 21740957 CCGGCCTTGGGTACGGCGGTACCCGGATGTGGAGTCGCTCTCGCCCGGCTGGGACTCTGTGGCGG CCGGCCTTGGGTACGGCGGTACCCGGATGTGGCGTCGCTCTCGCCCGGCTGGGACTCTGTGGCGG A C MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:21740906..21741032 26863196 MeRIP-seq:(Medium) rs984440995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_505404,Human_RBP_ID_5369172,Human_RBP_ID_8828866,Human_RBP_ID_9290965,Human_RBP_ID_18460676,Human_RBP_ID_22445867 RMVar_hsa_circ_82071,RMVar_hsa_circ_102856,RMVar_hsa_circ_189017,RMVar_hsa_circ_189018 65270 RMVar_ID_65270 Human_SNP_ID_640235174 m1A Human chr18 - 21812447 21812447 21812447 TTCTTACTCACCTGGATGATTACCACAACTCAACCTCCCTTCACTTTCTTATCCCAATCTATTCT TTCTTACTCACCTGGATGATTACCACAACTCAGCCTCCCTTCACTTTCTTATCCCAATCTATTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:21812397..21812594 26863196 MeRIP-seq:(Medium) rs983503247 Functional Loss SNV dbSNP153 33..33 33 - - - 65271 RMVar_ID_65271 Human_SNP_ID_640235176 m1A Human chr18 - 21812461 21812460 21812461 AATTCAGGCCTTCATTCTTACTCACCTGGATGATTACCACAACTCAACCTCCCTTCACTTTCTTA AATTCAGGCCTTCATTCTTACTCACCTGGATG_TTACCACAACTCAACCTCCCTTCACTTTCTTA AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:21812411..21812541 26863196 MeRIP-seq:(Medium) rs1350585348 Functional Loss DEL dbSNP153 33..33 33 - - - 65272 RMVar_ID_65272 Human_SNP_ID_640248364 m1A Human chr18 - 21866645 21866645 21866645 CAGCTCAGAAAACAGAAAGGATTTGTTTAAGGAAAGTAGAGCTGGAGACCACACAATTCTCTGAT CAGCTCAGAAAACAGAAAGGATTTGTTTAAGGGAAGTAGAGCTGGAGACCACACAATTCTCTGAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:21866541..21866651 32194978 MeRIP-seq:(Medium) rs1002872399 Functional Loss SNV dbSNP153 33..33 33 - - - 65273 RMVar_ID_65273 Human_SNP_ID_640248365 m1A Human chr18 - 21866645 21866645 21866645 CAGCTCAGAAAACAGAAAGGATTTGTTTAAGGAAAGTAGAGCTGGAGACCACACAATTCTCTGAT CAGCTCAGAAAACAGAAAGGATTTGTTTAAGGCAAGTAGAGCTGGAGACCACACAATTCTCTGAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:21866541..21866651 32194978 MeRIP-seq:(Medium) rs1002872399 Functional Loss SNV dbSNP153 33..33 33 - - - 65274 RMVar_ID_65274 Human_SNP_ID_640323712 m1A Human chr18 - 22170082 22170082 22170082 CTCGGAGCGAGTGGGGGAGGGAGGTGAAATGCAGCCGGGCTGGCCTCCTCCAGGCTGCTCTTCCA CTCGGAGCGAGTGGGGGAGGGAGGTGAAATGCGGCCGGGCTGGCCTCCTCCAGGCTGCTCTTCCA T C GATA6-AS1,GATA6-AS1:2 RNACentral:URS00008C2474,RNACentral:URS0000D5A41A lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:22170061..22170227 26863196 MeRIP-seq:(Medium) rs1204081886 Functional Loss SNV dbSNP153 33..33 33 - - - 65275 RMVar_ID_65275 Human_SNP_ID_640324339 m1A Human chr18 + 22171675 22171675 22171675 GGCGGCTTCGTGCACTCTGCGGCCGCGGCGGCAGCAGCCGCGGCGGCGGCCAGCTCCCCGGTCTA GGCGGCTTCGTGCACTCTGCGGCCGCGGCGGCGGCAGCCGCGGCGGCGGCCAGCTCCCCGGTCTA A G GATA6 Ensembl:ENSG00000141448 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:22171541..22171710 26863410 MeRIP-seq:(Medium) rs1385413802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4483864,Human_RBP_ID_22063545 65276 RMVar_ID_65276 Human_SNP_ID_640324401 m1A Human chr18 - 22171870 22171858 22171870 CCAGCGCCGCCAGGCCCCGCGGCCCCGCCGCCAGCCGCGCCGCCTCCGCTGCCGTATGGAGGGCT CCAGCGCCGCCAGGCCCCGCGGCCCCGCCGCC____________TCCGCTGCCGTATGGAGGGCT AGGCGGCGCGGCT A GATA6-AS1 RNACentral:URS0000D5A41A lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:22171820..22171895 26863196 MeRIP-seq:(Medium) rs1195209193 Functional Loss DEL dbSNP153 33..44 33 - - - 65277 RMVar_ID_65277 Human_SNP_ID_640324404 m1A Human chr18 - 22171870 22171870 22171870 CCAGCGCCGCCAGGCCCCGCGGCCCCGCCGCCAGCCGCGCCGCCTCCGCTGCCGTATGGAGGGCT CCAGCGCCGCCAGGCCCCGCGGCCCCGCCGCCGGCCGCGCCGCCTCCGCTGCCGTATGGAGGGCT T C GATA6-AS1 RNACentral:URS0000D5A41A lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:22171820..22171895 26863196 MeRIP-seq:(Medium) rs1310939981 Functional Loss SNV dbSNP153 33..33 33 - - - 65278 RMVar_ID_65278 Human_SNP_ID_640368597 m1A Human chr18 - 22348422 22348418 22348422 GCTTGGTGGGGGTGAGGGGAGCAGAAAGAGAGAGAGTTTGGTCCCCAAGTATTGAGCTGTGAGAG GCTTGGTGGGGGTGAGGGGAGCAGAAAGAGAG____TTTGGTCCCCAAGTATTGAGCTGTGAGAG ACTCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:22348371..22348485 26863196 MeRIP-seq:(Medium) rs545246536 Functional Loss DEL dbSNP153 33..36 33 - - - 65279 RMVar_ID_65279 Human_SNP_ID_640368598 m1A Human chr18 - 22348422 22348418 22348422 GCTTGGTGGGGGTGAGGGGAGCAGAAAGAGAGAGAGTTTGGTCCCCAAGTATTGAGCTGTGAGAG GCTTGGTGGGGGTGAGGGGAGCAGAAAGAGAG__AGTTTGGTCCCCAAGTATTGAGCTGTGAGAG ACTCT ACT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:22348371..22348485 26863196 MeRIP-seq:(Medium) rs545246536 Functional Loss DEL dbSNP153 33..34 33 - - - 65280 RMVar_ID_65280 Human_SNP_ID_640504828 m1A Human chr18 + 22933966 22933966 22933966 GAAAGCCTTTGCCCCGCTGCTCTGCTCCGCCCATAAGAGGACCCCTGAAATGTCCCGTGCAGTTT GAAAGCCTTTGCCCCGCTGCTCTGCTCCGCCCGTAAGAGGACCCCTGAAATGTCCCGTGCAGTTT A G RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:22933915..22934026;chr18:22933915..22934006 26863196 MeRIP-seq:(Medium) rs968310584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4483956,Human_RBP_ID_18440061,Human_RBP_ID_23762757,Human_RBP_ID_26977913 65281 RMVar_ID_65281 Human_SNP_ID_640555316 m1A Human chr18 - 23135225 23135225 23135225 CTGTCCGGGTTGTCGGAGCTGCCTGCTGGGAGAGTTGGCGACTCCCGGGGCCGCGGAAGCCAGGT CTGTCCGGGTTGTCGGAGCTGCCTGCTGGGAGCGTTGGCGACTCCCGGGGCCGCGGAAGCCAGGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:23135182..23135320 26863196 MeRIP-seq:(Medium) rs1018718092 Functional Loss SNV dbSNP153 33..33 33 - - - 65282 RMVar_ID_65282 Human_SNP_ID_640555339 m1A Human chr18 + 23135281 23135281 23135281 CCCGGACAGCCGGGCCGATCCCCCGCCCCACCACCCGCTCGGCTCTCGCGTCCTCCTCTTCCTCC CCCGGACAGCCGGGCCGATCCCCCGCCCCACCCCCCGCTCGGCTCTCGCGTCCTCCTCTTCCTCC A C CABLES1 Ensembl:ENSG00000134508 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23135234..23135318 26863196 MeRIP-seq:(Medium) rs561301359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189096,RMVar_hsa_circ_81692 65283 RMVar_ID_65283 Human_SNP_ID_640555827 m1A Human chr18 - 23136402 23136402 23136402 AAAGGCGGCCGCCGGCACCTGCACGCTGATAAAGGCATCGTCCTCCTCCAACTCCTCCTGCCCGG AAAGGCGGCCGCCGGCACCTGCACGCTGATAACGGCATCGTCCTCCTCCAACTCCTCCTGCCCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23136351..23136477 26863196 MeRIP-seq:(Medium) rs991437774 Functional Loss SNV dbSNP153 33..33 33 - - - 65284 RMVar_ID_65284 Human_SNP_ID_640559834 m1A Human chr18 + 23151953 23151952 23151954 GAAGCGGGTGGAGAGAAGTGAACGGACTCAACAGAGATGAAAGGCACAATGGAGATGGATTAGAT GAAGCGGGTGGAGAGAAGTGAACGGACTCAAC__AGATGAAAGGCACAATGGAGATGGATTAGAT CAG C CABLES1 Ensembl:ENSG00000134508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23151660..23152074 26863196 MeRIP-seq:(Medium) rs543729025 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_189096,RMVar_hsa_circ_81692 65285 RMVar_ID_65285 Human_SNP_ID_640562661 m1A Human chr18 + 23163490 23163490 23163490 AGTAGAAGAGCACCTAGCAACAAAACCAGGACAGGGTAGCCTGGATGTGGGAGGAGAAGCAGGCA AGTAGAAGAGCACCTAGCAACAAAACCAGGACGGGGTAGCCTGGATGTGGGAGGAGAAGCAGGCA A G CABLES1 Ensembl:ENSG00000134508 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:23163463..23163611 26863196 MeRIP-seq:(Medium) rs903125657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189096,RMVar_hsa_circ_81692 65286 RMVar_ID_65286 Human_SNP_ID_640572319 m1A Human chr18 - 23201803 23201801 23201803 CTGGCTGCCTCAGTCTCTCTCCATGGCACATTATCTCATCTTTCACCTGTGCACATGTATCATTT CTGGCTGCCTCAGTCTCTCTCCATGGCACATT__CTCATCTTTCACCTGTGCACATGTATCATTT GAT G TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:23201801..23202056 26863196 MeRIP-seq:(Medium) rs933703346 Functional Loss DEL dbSNP153 33..34 33 - - - 65287 RMVar_ID_65287 Human_SNP_ID_640572321 m1A Human chr18 - 23201803 23201803 23201803 CTGGCTGCCTCAGTCTCTCTCCATGGCACATTATCTCATCTTTCACCTGTGCACATGTATCATTT CTGGCTGCCTCAGTCTCTCTCCATGGCACATTTTCTCATCTTTCACCTGTGCACATGTATCATTT T A TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:23201801..23202056 26863196 MeRIP-seq:(Medium) rs896912010 Functional Loss SNV dbSNP153 33..33 33 - - - 65288 RMVar_ID_65288 Human_SNP_ID_640589028 m1A Human chr18 - 23267687 23267687 23267687 GAAAGAGGATGGGGCAGGGGACCCCAGATGTGAAGCAGAGGTGCAGAGGAACGGGACAGAGTCAG GAAAGAGGATGGGGCAGGGGACCCCAGATGTGTAGCAGAGGTGCAGAGGAACGGGACAGAGTCAG T A TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23267642..23267719 26863196 MeRIP-seq:(Medium) rs923660189 Functional Loss SNV dbSNP153 33..33 33 - - - 65289 RMVar_ID_65289 Human_SNP_ID_640596137 m1A Human chr18 - 23296522 23296522 23296522 AAGCAGATCACCTGAGGTCGGGAGTTCAAGACAAACCTGGCCAACATGGTGAAACCCTGTCTCTA AAGCAGATCACCTGAGGTCGGGAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCTGTCTCTA T G TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9954334 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7898,GWAS_ID_7899,GWAS_ID_7900,GWAS_ID_7901,GWAS_ID_7902,GWAS_ID_7903,GWAS_ID_7904 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102 65290 RMVar_ID_65290 Human_SNP_ID_640598688 m1A Human chr18 - 23307908 23307865 23307909 GACAGGCAGGCTCTTCAGAAGGATGGCTGAGCAGGGCAGATGGGGACAGGTGGGTTCTTCAGAAG GACAGGCAGGCTCTTCAGAAGGATGGCTGAG__________________________________ CCTCAGCCATCCTTCTGAAGAACCCACCTGTCCCCATCTGCCCTG C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23307895..23307993 26863196 MeRIP-seq:(Medium) rs1377925065 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_6674201 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102,RMVar_hsa_circ_4873 65291 RMVar_ID_65291 Human_SNP_ID_640598690 m1A Human chr18 - 23307874 23307874 23307874 GGCAGATGGGGACAGGTGGGTTCTTCAGAAGGATGGCTGAGGCAGGGGCATGGCTGTGGGGAGAC GGCAGATGGGGACAGGTGGGTTCTTCAGAAGGGTGGCTGAGGCAGGGGCATGGCTGTGGGGAGAC T C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23307766..23307994 26863196 MeRIP-seq:(Medium) rs1344124049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13266719 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102,RMVar_hsa_circ_4873 65292 RMVar_ID_65292 Human_SNP_ID_640598698 m1A Human chr18 - 23307908 23307908 23307908 GACAGGCAGGCTCTTCAGAAGGATGGCTGAGCAGGGCAGATGGGGACAGGTGGGTTCTTCAGAAG GACAGGCAGGCTCTTCAGAAGGATGGCTGAGCGGGGCAGATGGGGACAGGTGGGTTCTTCAGAAG T C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23307895..23307993 26863196 MeRIP-seq:(Medium) rs907023307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6674201 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102,RMVar_hsa_circ_4873 65293 RMVar_ID_65293 Human_SNP_ID_640627806 m1A Human chr18 - 23434180 23434180 23434180 AGGAGAGGAGATGGGAGAGCCAGGTAGGTTGTACATTATGGGACTCTGGTGAGGAACTTTATATC AGGAGAGGAGATGGGAGAGCCAGGTAGGTTGTTCATTATGGGACTCTGGTGAGGAACTTTATATC T A TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23434178..23434352 26863196 MeRIP-seq:(Medium) rs976748660 Functional Loss SNV dbSNP153 33..33 33 - - - 65294 RMVar_ID_65294 Human_SNP_ID_640628672 m1A Human chr18 - 23437903 23437902 23437903 GCTGCTGCTGCTGCGGGGGTCGGGCGGCGGCCAGGGGATTTGGGCAGGCACCGTGGATCCCCGAG GCTGCTGCTGCTGCGGGGGTCGGGCGGCGGCC_GGGGATTTGGGCAGGCACCGTGGATCCCCGAG CT C TMEM241 Ensembl:ENSG00000134490 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23437808..23437907 26863196 MeRIP-seq:(Medium) rs1371777261 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4484143,Human_RBP_ID_17907623,Human_RBP_ID_18420656 65295 RMVar_ID_65295 Human_SNP_ID_640632754 m1A Human chr18 - 23453521 23453521 23453521 GATCCAGCCCGTGTGACCAAGGCTAGTACTCCAGTCTCGTCTGCCACTTACCTTGCTGGGTCCCC GATCCAGCCCGTGTGACCAAGGCTAGTACTCCGGTCTCGTCTGCCACTTACCTTGCTGGGTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23453520..23453633 26863196 MeRIP-seq:(Medium) rs1414334693 Functional Loss SNV dbSNP153 33..33 33 - - - 65296 RMVar_ID_65296 Human_SNP_ID_640632755 m1A Human chr18 - 23453521 23453521 23453521 GATCCAGCCCGTGTGACCAAGGCTAGTACTCCAGTCTCGTCTGCCACTTACCTTGCTGGGTCCCC GATCCAGCCCGTGTGACCAAGGCTAGTACTCCCGTCTCGTCTGCCACTTACCTTGCTGGGTCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23453520..23453633 26863196 MeRIP-seq:(Medium) rs1414334693 Functional Loss SNV dbSNP153 33..33 33 - - - 65297 RMVar_ID_65297 Human_SNP_ID_640666514 m1A Human chr18 - 23576628 23576627 23576628 AAAACATCTGAACATCAGAAGGGACAGATTCCAGACGCGCCACCTTAAGAGCTGTAACGCTCACC AAAACATCTGAACATCAGAAGGGACAGATTCC_GACGCGCCACCTTAAGAGCTGTAACGCTCACC CT C NPC1 Ensembl:ENSG00000141458 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:23576530..23576640 26863196 MeRIP-seq:(Medium) rs1360138841 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_189159,RMVar_hsa_circ_86032 65298 RMVar_ID_65298 Human_SNP_ID_640683621 m1A Human chr18 - 23649192 23649192 23649192 TTTAAGATCCTGTTTCATTTTGTTCTTGCAGAAGGAAACTCCACTTGCCAATGCTGCATTCTGGG TTTAAGATCCTGTTTCATTTTGTTCTTGCAGAGGGAAACTCCACTTGCCAATGCTGCATTCTGGG T C ANKRD29 Ensembl:ENSG00000154065 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23649141..23649228 26863196 MeRIP-seq:(Medium) rs894934365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1899994,Human_Splice_Rec_1900022,Human_Splice_Rec_1900054,Human_Splice_Rec_1900062 RMVar_hsa_circ_189166,RMVar_hsa_circ_125704 65299 RMVar_ID_65299 Human_SNP_ID_640686792 m1A Human chr18 - 23662764 23662764 23662764 AGGGCCGGGGAGGACAAGGCGCCCCGGGCCCAAAGCGCGCCGGCTCCCGCTCGGGCGGCCGCGGA AGGGCCGGGGAGGACAAGGCGCCCCGGGCCCACAGCGCGCCGGCTCCCGCTCGGGCGGCCGCGGA T G ANKRD29 Ensembl:ENSG00000154065 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr18:23649099..23662900;chr18:23662676..23662869 26863196 MeRIP-seq:(Medium) rs1315498672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1899993,Human_Splice_Rec_1900021,Human_Splice_Rec_1900053,Human_Splice_Rec_1900061 65300 RMVar_ID_65300 Human_SNP_ID_640693510 m1A Human chr18 + 23689684 23689684 23689684 ACGGCTCAGGCGGGAGGACCCCGCGCGGCTGGATGGCGGCGGCCGCGCGGCCTCGGGGTCGGGCA ACGGCTCAGGCGGGAGGACCCCGCGCGGCTGGCTGGCGGCGGCCGCGCGGCCTCGGGGTCGGGCA A C LAMA3 Ensembl:ENSG00000053747 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23689641..23689749 26863196 MeRIP-seq:(Medium) rs1336956535 Functional Loss SNV dbSNP153 33..33 33 - - - 65301 RMVar_ID_65301 Human_SNP_ID_640712887 m1A Human chr18 + 23778665 23778665 23778665 CAGCACACGCACACAGCCCACGACTGGGCACCATCGGACTCATGCTCACATCTCCTGAGTTTGCC CAGCACACGCACACAGCCCACGACTGGGCACCCTCGGACTCATGCTCACATCTCCTGAGTTTGCC A C LAMA3 Ensembl:ENSG00000053747 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23778616..23778854 26863196 MeRIP-seq:(Medium) rs117577979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6674706 RMVar_hsa_circ_6156,RMVar_hsa_circ_89398,RMVar_hsa_circ_105386,RMVar_hsa_circ_189170,RMVar_hsa_circ_127730,RMVar_hsa_circ_189172,RMVar_hsa_circ_85340,RMVar_hsa_circ_189173,RMVar_hsa_circ_189171,RMVar_hsa_circ_45422,RMVar_hsa_circ_120197,RMVar_hsa_circ_266897,RMVar_hsa_circ_104266,RMVar_hsa_circ_189174,RMVar_hsa_circ_28286,RMVar_hsa_circ_80693,RMVar_hsa_circ_189175,RMVar_hsa_circ_335922,RMVar_hsa_circ_189176,RMVar_hsa_circ_189177,RMVar_hsa_circ_372700,RMVar_hsa_circ_189178 65302 RMVar_ID_65302 Human_SNP_ID_640712888 m1A Human chr18 + 23778665 23778665 23778665 CAGCACACGCACACAGCCCACGACTGGGCACCATCGGACTCATGCTCACATCTCCTGAGTTTGCC CAGCACACGCACACAGCCCACGACTGGGCACCGTCGGACTCATGCTCACATCTCCTGAGTTTGCC A G LAMA3 Ensembl:ENSG00000053747 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23778616..23778854 26863196 MeRIP-seq:(Medium) rs117577979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6674706 RMVar_hsa_circ_6156,RMVar_hsa_circ_89398,RMVar_hsa_circ_105386,RMVar_hsa_circ_189170,RMVar_hsa_circ_127730,RMVar_hsa_circ_189172,RMVar_hsa_circ_85340,RMVar_hsa_circ_189173,RMVar_hsa_circ_189171,RMVar_hsa_circ_45422,RMVar_hsa_circ_120197,RMVar_hsa_circ_266897,RMVar_hsa_circ_104266,RMVar_hsa_circ_189174,RMVar_hsa_circ_28286,RMVar_hsa_circ_80693,RMVar_hsa_circ_189175,RMVar_hsa_circ_335922,RMVar_hsa_circ_189176,RMVar_hsa_circ_189177,RMVar_hsa_circ_372700,RMVar_hsa_circ_189178 65303 RMVar_ID_65303 Human_SNP_ID_640727720 m1A Human chr18 + 23844968 23844968 23844968 ACCTGTATAATAAGTAGCCTTAGGTCTGTGTCATCATTGGAAATTCTAAGACATGCTGGTGGATT ACCTGTATAATAAGTAGCCTTAGGTCTGTGTCGTCATTGGAAATTCTAAGACATGCTGGTGGATT A G LAMA3 Ensembl:ENSG00000053747 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23844966..23845077 26863196 MeRIP-seq:(Medium) rs1252482358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53988,RMVar_hsa_circ_105386,RMVar_hsa_circ_189170,RMVar_hsa_circ_127730,RMVar_hsa_circ_189172,RMVar_hsa_circ_85340,RMVar_hsa_circ_189173,RMVar_hsa_circ_104266,RMVar_hsa_circ_189175,RMVar_hsa_circ_84029,RMVar_hsa_circ_189179,RMVar_hsa_circ_122129,RMVar_hsa_circ_106223,RMVar_hsa_circ_265320,RMVar_hsa_circ_127411,RMVar_hsa_circ_189181,RMVar_hsa_circ_189182,RMVar_hsa_circ_189183,RMVar_hsa_circ_82055,RMVar_hsa_circ_189184,RMVar_hsa_circ_87137,RMVar_hsa_circ_112354,RMVar_hsa_circ_189186,RMVar_hsa_circ_77596,RMVar_hsa_circ_189188,RMVar_hsa_circ_81029,RMVar_hsa_circ_189187,RMVar_hsa_circ_111716,RMVar_hsa_circ_189189,RMVar_hsa_circ_189191,RMVar_hsa_circ_79545,RMVar_hsa_circ_189190 65304 RMVar_ID_65304 Human_SNP_ID_640759568 m1A Human chr18 + 23982798 23982795 23982799 TTCTTTCCCTTTCTTACACTGACACACTACCTAACTTTCTATCAAATCCTCCTGCGCTATAGAAG TTCTTTCCCTTTCTTACACTGACACACTAC____CTTTCTATCAAATCCTCCTGCGCTATAGAAG CCTAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:23982659..23982805 26863196 MeRIP-seq:(Medium) rs1485181598 Functional Loss DEL dbSNP153 31..34 33 - - - 65305 RMVar_ID_65305 Human_SNP_ID_640766741 m1A Human chr18 + 24014825 24014825 24014825 AGCCGGGCTCCGGGCGCGCGCGGGGCCGCAGCAGCTGCTCCCGATCTCGCCTCGGCCCAGCGCAG AGCCGGGCTCCGGGCGCGCGCGGGGCCGCAGCTGCTGCTCCCGATCTCGCCTCGGCCCAGCGCAG A T TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr18:24014776..24014915;chr18:24014776..24014950 26863196 MeRIP-seq:(Medium) rs1402491405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238665,Human_RBP_ID_17907743,Human_RBP_ID_18944254 RMVar_hsa_circ_101898,RMVar_hsa_circ_189245 65306 RMVar_ID_65306 Human_SNP_ID_640773277 m1A Human chr18 + 24041341 24041340 24041341 ATTGATTCGCTAGCACAGGAAGAGAAAGCTGGAGGCTTTTGAGAACTCTGGGCTCCACCTTGCAG ATTGATTCGCTAGCACAGGAAGAGAAAGCTGG_GGCTTTTGAGAACTCTGGGCTCCACCTTGCAG GA G TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:24041325..24041450 26863196 MeRIP-seq:(Medium) rs1568415366 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_95582,RMVar_hsa_circ_189247 65307 RMVar_ID_65307 Human_SNP_ID_640773278 m1A Human chr18 + 24041341 24041341 24041341 ATTGATTCGCTAGCACAGGAAGAGAAAGCTGGAGGCTTTTGAGAACTCTGGGCTCCACCTTGCAG ATTGATTCGCTAGCACAGGAAGAGAAAGCTGGGGGCTTTTGAGAACTCTGGGCTCCACCTTGCAG A G TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:24041325..24041450 26863196 MeRIP-seq:(Medium) rs12967198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_95582,RMVar_hsa_circ_189247 65308 RMVar_ID_65308 Human_SNP_ID_640773279 m1A Human chr18 + 24041341 24041341 24041341 ATTGATTCGCTAGCACAGGAAGAGAAAGCTGGAGGCTTTTGAGAACTCTGGGCTCCACCTTGCAG ATTGATTCGCTAGCACAGGAAGAGAAAGCTGGTGGCTTTTGAGAACTCTGGGCTCCACCTTGCAG A T TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:24041325..24041450 26863196 MeRIP-seq:(Medium) rs12967198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_95582,RMVar_hsa_circ_189247 65309 RMVar_ID_65309 Human_SNP_ID_640779105 m1A Human chr18 + 24065029 24065029 24065029 AAATGGTACTGGGTGGCGGTTGTAACATTAGTACCCAAGTGATAACAAGGGCTGCGAATGAGATC AAATGGTACTGGGTGGCGGTTGTAACATTAGTGCCCAAGTGATAACAAGGGCTGCGAATGAGATC A G TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:24065018..24065260 26863196 MeRIP-seq:(Medium) rs1304888191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68827,RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_95582,RMVar_hsa_circ_189247,RMVar_hsa_circ_273917,RMVar_hsa_circ_304158,RMVar_hsa_circ_329102,RMVar_hsa_circ_368637,RMVar_hsa_circ_313099,RMVar_hsa_circ_297157,RMVar_hsa_circ_270652,RMVar_hsa_circ_189248,RMVar_hsa_circ_189250,RMVar_hsa_circ_189252,RMVar_hsa_circ_189253,RMVar_hsa_circ_189251,RMVar_hsa_circ_189249 65310 RMVar_ID_65310 Human_SNP_ID_640821461 m1A Human chr18 - 24237996 24237993 24237997 ATTATTAATAGAGGTTTGATAGAAGTAAAAGAAAGGGAAGAAGTAATTTTCATAGCCAGATTTGG ATTATTAATAGAGGTTTGATAGAAGTAAAAG____GGAAGAAGTAATTTTCATAGCCAGATTTGG CCTTT C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:24237990..24238185 26863196 MeRIP-seq:(Medium) rs1267749186 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_20957,RMVar_hsa_circ_358895,RMVar_hsa_circ_66347,RMVar_hsa_circ_189283,RMVar_hsa_circ_93897,RMVar_hsa_circ_110856,RMVar_hsa_circ_189284,RMVar_hsa_circ_326445,RMVar_hsa_circ_270323,RMVar_hsa_circ_315467,RMVar_hsa_circ_189285,RMVar_hsa_circ_16773,RMVar_hsa_circ_348489,RMVar_hsa_circ_378943,RMVar_hsa_circ_340410,RMVar_hsa_circ_52837,RMVar_hsa_circ_290747,RMVar_hsa_circ_35052,RMVar_hsa_circ_189286,RMVar_hsa_circ_189287 65311 RMVar_ID_65311 Human_SNP_ID_640829510 m1A Human chr18 - 24271554 24271554 24271554 GGGCAGCCTGGGGCCACGGAGGACGCCGGGGGACGGAGCGGGGAGGGCGGCCAGACTTGATCCAG GGGCAGCCTGGGGCCACGGAGGACGCCGGGGGCCGGAGCGGGGAGGGCGGCCAGACTTGATCCAG T G OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:24271552..24271694 26863196 MeRIP-seq:(Medium) rs1388242828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1901133 RMVar_hsa_circ_20957,RMVar_hsa_circ_66347,RMVar_hsa_circ_189283,RMVar_hsa_circ_93897,RMVar_hsa_circ_110856,RMVar_hsa_circ_189284,RMVar_hsa_circ_326445,RMVar_hsa_circ_315467,RMVar_hsa_circ_16773,RMVar_hsa_circ_348489,RMVar_hsa_circ_378943,RMVar_hsa_circ_340410,RMVar_hsa_circ_52837,RMVar_hsa_circ_35052,RMVar_hsa_circ_189288,RMVar_hsa_circ_189286,RMVar_hsa_circ_303778,RMVar_hsa_circ_313030,RMVar_hsa_circ_53514 65312 RMVar_ID_65312 Human_SNP_ID_640829622 m1A Human chr18 - 24271959 24271959 24271959 CCGCCCGCCCGCGCTCTCCCCGCGAGCCCCGGAGGGCGGGTCTGCGGCCGAGCCAGCGGCGGCGG CCGCCCGCCCGCGCTCTCCCCGCGAGCCCCGGGGGGCGGGTCTGCGGCCGAGCCAGCGGCGGCGG T C OSBPL1A Ensembl:ENSG00000141447 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:24271912..24272180 26863196 MeRIP-seq:(Medium) rs975328613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20957,RMVar_hsa_circ_66347,RMVar_hsa_circ_189283,RMVar_hsa_circ_93897,RMVar_hsa_circ_110856,RMVar_hsa_circ_189284,RMVar_hsa_circ_326445,RMVar_hsa_circ_315467,RMVar_hsa_circ_16773,RMVar_hsa_circ_348489,RMVar_hsa_circ_378943,RMVar_hsa_circ_340410,RMVar_hsa_circ_52837,RMVar_hsa_circ_35052,RMVar_hsa_circ_189288,RMVar_hsa_circ_189286,RMVar_hsa_circ_303778,RMVar_hsa_circ_313030,RMVar_hsa_circ_53514 65313 RMVar_ID_65313 Human_SNP_ID_640842449 m1A Human chr18 + 24325520 24325519 24325520 TTCACTCCTGTACTCAACTCAGCTGTTTGCTCAAAGTTGCTTAGAGAGCCCTTCCTTTGCATCCC TTCACTCCTGTACTCAACTCAGCTGTTTGCTC_AAGTTGCTTAGAGAGCCCTTCCTTTGCATCCC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:24325477..24325617 26863196 MeRIP-seq:(Medium) rs1344198957 Functional Loss DEL dbSNP153 33..33 33 - - - 65314 RMVar_ID_65314 Human_SNP_ID_640849558 m1A Human chr18 + 24354881 24354881 24354881 TTCTATTAACCGTTTCCTTAACTCTGCAGGTCAGCCCTCCCACTGTTCCCTGCTGAACCTGCCAC TTCTATTAACCGTTTCCTTAACTCTGCAGGTCGGCCCTCCCACTGTTCCCTGCTGAACCTGCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:24354877..24354963 26863196 MeRIP-seq:(Medium) rs899702191 Functional Loss SNV dbSNP153 33..33 33 - - - 65315 RMVar_ID_65315 Human_SNP_ID_640854980 m1A Human chr18 - 24377523 24377522 24377524 TTATTATTTTCTTAATTTAGAAATGAACACAGAAGCGGAGCAACAGCTTCTCCATCACGCCAGAA TTATTATTTTCTTAATTTAGAAATGAACACA__AGCGGAGCAACAGCTTCTCCATCACGCCAGAA TTC T OSBPL1A Ensembl:ENSG00000141447 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:24377472..24397857 26863196 MeRIP-seq:(Medium) rs1187097687 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1901026,Human_Splice_Rec_1901156,Human_Splice_Rec_1901180,Human_Splice_Rec_1901206,Human_Splice_Rec_1901218,Human_Splice_Rec_1901222,Human_Splice_Rec_1901230,Human_Splice_Rec_1901238 RMVar_hsa_circ_52837,RMVar_hsa_circ_312310,RMVar_hsa_circ_189293,RMVar_hsa_circ_367810,RMVar_hsa_circ_189307,RMVar_hsa_circ_318594,RMVar_hsa_circ_314255 65316 RMVar_ID_65316 Human_SNP_ID_640867205 m1A Human chr18 - 24426745 24426745 24426745 CCCTGCGTCCCCCTCAGCCATGTGGCCCCTGGACCTGCCCTGCAGCCGCCGCCTGCCAGGTCCGG CCCTGCGTCCCCCTCAGCCATGTGGCCCCTGGCCCTGCCCTGCAGCCGCCGCCTGCCAGGTCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:24426696..24426835 26863196 MeRIP-seq:(Medium) rs1304271552 Functional Loss SNV dbSNP153 33..33 33 - - - 65317 RMVar_ID_65317 Human_SNP_ID_640867527 m1A Human chr18 + 24427877 24427877 24427877 ACCTTATAAAGTAGTAAGAATAGGATTTTAAGATGTGTACATTTGTTGACTTTTAAAAAATCAAT ACCTTATAAAGTAGTAAGAATAGGATTTTAAGTTGTGTACATTTGTTGACTTTTAAAAAATCAAT A T IMPACT Ensembl:ENSG00000154059 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:24427870..24427976 26863196 MeRIP-seq:(Medium) rs746846518 Functional Loss SNV dbSNP153 33..33 33 - - - 65318 RMVar_ID_65318 Human_SNP_ID_641058817 m1A Human chr18 - 25226989 25226989 25226989 CATGGAGCAGGTGCATAGCGGGGAGAAGAAGAACTCATGCAGCATTTGTTCTGAGAGTTTCCACA CATGGAGCAGGTGCATAGCGGGGAGAAGAAGAGCTCATGCAGCATTTGTTCTGAGAGTTTCCACA T C ZNF521 Ensembl:ENSG00000198795 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:25226942..25227070 26863196 MeRIP-seq:(Medium) rs767994488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189322,RMVar_hsa_circ_189320,RMVar_hsa_circ_375795,RMVar_hsa_circ_294616,RMVar_hsa_circ_326305,RMVar_hsa_circ_189323,RMVar_hsa_circ_297707,RMVar_hsa_circ_290811,RMVar_hsa_circ_303063,RMVar_hsa_circ_189324 65319 RMVar_ID_65319 Human_SNP_ID_641088739 m1A Human chr18 - 25351086 25351074 25351086 CCCGCGCGCGAGCGCGAGCCGGAGCCGGAGCGAGGAGCGGAGCGCGGAGCGAGGGCGCGAGGGAG CCCGCGCGCGAGCGCGAGCCGGAGCCGGAGCG____________CGGAGCGAGGGCGCGAGGGAG GCGCTCCGCTCCT G ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:25351038..25351191 26863196 MeRIP-seq:(Medium) rs1379012759 Functional Loss DEL dbSNP153 33..44 33 - - - 65320 RMVar_ID_65320 Human_SNP_ID_641088742 m1A Human chr18 - 25351078 25351078 25351078 CGAGCGCGAGCCGGAGCCGGAGCGAGGAGCGGAGCGCGGAGCGAGGGCGCGAGGGAGGCCGAGCG CGAGCGCGAGCCGGAGCCGGAGCGAGGAGCGGCGCGCGGAGCGAGGGCGCGAGGGAGGCCGAGCG T G ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:25351049..25351170 26863196 MeRIP-seq:(Medium) rs897225651 Functional Loss SNV dbSNP153 33..33 33 - - - 65321 RMVar_ID_65321 Human_SNP_ID_641088792 m1A Human chr18 - 25351175 25351175 25351175 GGGGGTCGAAGGCTGGGAAAGTTTGGTGCAGCAGCCGCCGCCGCCGCCGCCGCCGTCGTGCAGAG GGGGGTCGAAGGCTGGGAAAGTTTGGTGCAGCGGCCGCCGCCGCCGCCGCCGCCGTCGTGCAGAG T C ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:25351047..25351191 26863196 MeRIP-seq:(Medium) rs1187510901 Functional Loss SNV dbSNP153 33..33 33 - - - 65322 RMVar_ID_65322 Human_SNP_ID_641088793 m1A Human chr18 - 25351175 25351175 25351175 GGGGGTCGAAGGCTGGGAAAGTTTGGTGCAGCAGCCGCCGCCGCCGCCGCCGCCGTCGTGCAGAG GGGGGTCGAAGGCTGGGAAAGTTTGGTGCAGCCGCCGCCGCCGCCGCCGCCGCCGTCGTGCAGAG T G ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:25351047..25351191 26863196 MeRIP-seq:(Medium) rs1187510901 Functional Loss SNV dbSNP153 33..33 33 - - - 65323 RMVar_ID_65323 Human_SNP_ID_641089279 m1A Human chr18 - 25352164 25352164 25352164 TTAATCATGCCCCTCTGTCTGTGTGTGAGTGCAGGCAGGCTGACAATGATTTCCTCAGTGATTAC TTAATCATGCCCCTCTGTCTGTGTGTGAGTGCCGGCAGGCTGACAATGATTTCCTCAGTGATTAC T G ZNF521 Ensembl:ENSG00000198795 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:25352115..25352260 26863196 MeRIP-seq:(Medium) rs1220632586 Functional Loss SNV dbSNP153 33..33 33 - - - 65324 RMVar_ID_65324 Human_SNP_ID_641251364 m1A Human chr18 - 26035063 26035063 26035063 TACCAGGGACCACCTCCACAACAGGGATATCCACCCCAGCAGCAGCAGTACCCAGGGCAGCAAGG TACCAGGGACCACCTCCACAACAGGGATATCCGCCCCAGCAGCAGCAGTACCCAGGGCAGCAAGG T C SS18 Ensembl:ENSG00000141380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:26032497..26035170 32194978 MeRIP-seq:(Medium) rs751593410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_506180,Human_RBP_ID_17381603,Human_RBP_ID_22590005,Human_RBP_ID_25376659 Human_Splice_Rec_1901682,Human_Splice_Rec_1901683,Human_Splice_Rec_1901702,Human_Splice_Rec_1901703,Human_Splice_Rec_1901722,Human_Splice_Rec_1901723,Human_Splice_Rec_1901740,Human_Splice_Rec_1901741,Human_Splice_Rec_1901758,Human_Splice_Rec_1901759,Human_Splice_Rec_1901778,Human_Splice_Rec_1901779,Human_Splice_Rec_1901783,Human_Splice_Rec_1901787,Human_Splice_Rec_1901804 Human_miRNA_ID_2685980 RMVar_hsa_circ_22229,RMVar_hsa_circ_112160,RMVar_hsa_circ_189335,RMVar_hsa_circ_189334,RMVar_hsa_circ_105052,RMVar_hsa_circ_189333,RMVar_hsa_circ_189336,RMVar_hsa_circ_189337,RMVar_hsa_circ_272454,RMVar_hsa_circ_308483,RMVar_hsa_circ_189338,RMVar_hsa_circ_321444,RMVar_hsa_circ_305802,RMVar_hsa_circ_57519,RMVar_hsa_circ_45999,RMVar_hsa_circ_75773,RMVar_hsa_circ_119007,RMVar_hsa_circ_189339,RMVar_hsa_circ_189341,RMVar_hsa_circ_189340,RMVar_hsa_circ_304018,RMVar_hsa_circ_331291,RMVar_hsa_circ_125700,RMVar_hsa_circ_96027,RMVar_hsa_circ_189344,RMVar_hsa_circ_189346,RMVar_hsa_circ_43068,RMVar_hsa_circ_189345,RMVar_hsa_circ_189343 65325 RMVar_ID_65325 Human_SNP_ID_641257106 m1A Human chr18 - 26057609 26057609 26057609 TGGGGGTCCTCCTGCACCGCACATGCAGAACCAGATGAACGGCCAGATGCCTGGTAAGTTTTTCT TGGGGGTCCTCCTGCACCGCACATGCAGAACCGGATGAACGGCCAGATGCCTGGTAAGTTTTTCT T C SS18 Ensembl:ENSG00000141380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:26052711..26068282 32194978 MeRIP-seq:(Medium) rs1263918515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769037,Human_RBP_ID_906239,Human_RBP_ID_5583111,Human_RBP_ID_13272725,Human_RBP_ID_17381604,Human_RBP_ID_18993644 Human_Splice_Rec_1901673,Human_Splice_Rec_1901693,Human_Splice_Rec_1901715,Human_Splice_Rec_1901731,Human_Splice_Rec_1901751,Human_Splice_Rec_1901771,Human_Splice_Rec_1901795,Human_Splice_Rec_1901813,Human_Splice_Rec_1901825,Human_Splice_Rec_1901831,Human_Splice_Rec_1901841,Human_Splice_Rec_1901849,Human_Splice_Rec_1901859 RMVar_hsa_circ_189336,RMVar_hsa_circ_189337,RMVar_hsa_circ_272454,RMVar_hsa_circ_189338,RMVar_hsa_circ_321444,RMVar_hsa_circ_305802,RMVar_hsa_circ_59866,RMVar_hsa_circ_75773,RMVar_hsa_circ_119007,RMVar_hsa_circ_189339,RMVar_hsa_circ_189341,RMVar_hsa_circ_189340,RMVar_hsa_circ_304018,RMVar_hsa_circ_331291,RMVar_hsa_circ_189346,RMVar_hsa_circ_189345,RMVar_hsa_circ_346518,RMVar_hsa_circ_326237,RMVar_hsa_circ_5770,RMVar_hsa_circ_189347,RMVar_hsa_circ_272775,RMVar_hsa_circ_282793,RMVar_hsa_circ_347741,RMVar_hsa_circ_281431,RMVar_hsa_circ_63002,RMVar_hsa_circ_189349,RMVar_hsa_circ_189350,RMVar_hsa_circ_299711,RMVar_hsa_circ_189348,RMVar_hsa_circ_317532,RMVar_hsa_circ_287404,RMVar_hsa_circ_189353,RMVar_hsa_circ_9789,RMVar_hsa_circ_189352 65326 RMVar_ID_65326 Human_SNP_ID_641265762 m1A Human chr18 - 26091038 26091037 26091039 CTGAACTAGGTCTAGGGCACGCTCTGCAACACAGTCGGGGAGACGCTTCAGAGGGCCGGAGAGGG CTGAACTAGGTCTAGGGCACGCTCTGCAACA__GTCGGGGAGACGCTTCAGAGGGCCGGAGAGGG CTG C SS18 Ensembl:ENSG00000141380 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:26091031..26091164 26863196 MeRIP-seq:(Medium) rs1338349870 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_75773,RMVar_hsa_circ_189346 65327 RMVar_ID_65327 Human_SNP_ID_641265763 m1A Human chr18 - 26091038 26091038 26091038 CTGAACTAGGTCTAGGGCACGCTCTGCAACACAGTCGGGGAGACGCTTCAGAGGGCCGGAGAGGG CTGAACTAGGTCTAGGGCACGCTCTGCAACACCGTCGGGGAGACGCTTCAGAGGGCCGGAGAGGG T G SS18 Ensembl:ENSG00000141380 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:26091031..26091164 26863196 MeRIP-seq:(Medium) rs1348387599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75773,RMVar_hsa_circ_189346 65328 RMVar_ID_65328 Human_SNP_ID_641296798 m1A Human chr18 - 26226509 26226509 26226509 AAATTTCAAAACTACGAACCCCGAGTGCCCACAGCCCCCTACGCGCGATTGGCACGGCCCCGCCG AAATTTCAAAACTACGAACCCCGAGTGCCCACTGCCCCCTACGCGCGATTGGCACGGCCCCGCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:26226461..26227007 26863196 MeRIP-seq:(Medium) rs1362766976 Functional Loss SNV dbSNP153 33..33 33 - - - 65329 RMVar_ID_65329 Human_SNP_ID_641363140 m1A Human chr18 - 26501247 26501247 26501247 AGTATCTAAACTTGCTTATCTCTCTGTAGGACAGTCGGCCCAATATGTCAAGACCTCTGATCACT AGTATCTAAACTTGCTTATCTCTCTGTAGGACGGTCGGCCCAATATGTCAAGACCTCTGATCACT T C KCTD1 Ensembl:ENSG00000134504 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:26501228..26501293 26863196 MeRIP-seq:(Medium) rs1166992507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906327 Human_Splice_Rec_1902102,Human_Splice_Rec_1902112,Human_Splice_Rec_1902120,Human_Splice_Rec_1902128,Human_Splice_Rec_1902136,Human_Splice_Rec_1902146,Human_Splice_Rec_1902158,Human_Splice_Rec_1902166 RMVar_hsa_circ_323239,RMVar_hsa_circ_189367,RMVar_hsa_circ_189368,RMVar_hsa_circ_91555 65330 RMVar_ID_65330 Human_SNP_ID_641374060 m1A Human chr18 + 26548223 26548223 26548223 CCAGCTCCTCCCCGGCCGAGTCCTCGGGCTCCAGGGGCTCGTCCCAGTCCAGCCCCATCTCCTCC CCAGCTCCTCCCCGGCCGAGTCCTCGGGCTCCGGGGGCTCGTCCCAGTCCAGCCCCATCTCCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:26548176..26548550 26863196 MeRIP-seq:(Medium) rs1302024891 Functional Loss SNV dbSNP153 33..33 33 - - - 65331 RMVar_ID_65331 Human_SNP_ID_641374248 m1A Human chr18 - 26548500 26548500 26548500 CGAGAATGCCTGGCAGCGGGGACTGTAACACCAGCGCGGGCGGCAGCGCCAGCGCTGCCGCCGCC CGAGAATGCCTGGCAGCGGGGACTGTAACACCGGCGCGGGCGGCAGCGCCAGCGCTGCCGCCGCC T C KCTD1 Ensembl:ENSG00000134504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:26548227..26548523 26863196 MeRIP-seq:(Medium) rs1448425680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4484823,Human_RBP_ID_5467833 RMVar_hsa_circ_189368,RMVar_hsa_circ_91555 65332 RMVar_ID_65332 Human_SNP_ID_641400234 m1A Human chr18 + 26657367 26657367 26657367 ACAAACCCAAACCGTCAGATCTTACCTGAAACATTGAAGCACAAAGTCTCTCTCCAAGTCCCCTT ACAAACCCAAACCGTCAGATCTTACCTGAAACCTTGAAGCACAAAGTCTCTCTCCAAGTCCCCTT A C AQP4-AS1 Ensembl:ENSG00000260372 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:26657244..26657366 26863196 MeRIP-seq:(Medium) rs1568023663 Functional Loss SNV dbSNP153 33..33 33 - - - 65333 RMVar_ID_65333 Human_SNP_ID_641757751 m1A Human chr18 + 28177057 28177057 28177057 AGGCGGAGAGGGGCCGAGCGAAGAGCCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGCGGAGGAGG AGGCGGAGAGGGGCCGAGCGAAGAGCCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGAGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:28177014..28177150 26863196 MeRIP-seq:(Medium) rs1365870906 Functional Loss SNV dbSNP153 33..33 33 - - - 65334 RMVar_ID_65334 Human_SNP_ID_641757798 m1A Human chr18 + 28177103 28177079 28177103 GCGGCGGCGGCGGAGGAGGAGGAGGCAGCGGCAGCACCAACAGCGGCGCGGAGAAACGGCTCCAG GCGGCGGCG________________________GCACCAACAGCGGCGCGGAGAAACGGCTCCAG GGCGGAGGAGGAGGAGGCAGCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:28177059..28177139 26863196 MeRIP-seq:(Medium) rs1179797321 Functional Loss DEL dbSNP153 10..33 33 - - - 65335 RMVar_ID_65335 Human_SNP_ID_641757833 m1A Human chr18 + 28177103 28177103 28177103 GCGGCGGCGGCGGAGGAGGAGGAGGCAGCGGCAGCACCAACAGCGGCGCGGAGAAACGGCTCCAG GCGGCGGCGGCGGAGGAGGAGGAGGCAGCGGCGGCACCAACAGCGGCGCGGAGAAACGGCTCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:28177059..28177139 26863196 MeRIP-seq:(Medium) rs1442896244 Functional Loss SNV dbSNP153 33..33 33 - - - 65336 RMVar_ID_65336 Human_SNP_ID_641757844 m1A Human chr18 + 28177122 28177122 28177122 AGGAGGCAGCGGCAGCACCAACAGCGGCGCGGAGAAACGGCTCCAGGCAGTTTCCACCCCCTTCC AGGAGGCAGCGGCAGCACCAACAGCGGCGCGGCGAAACGGCTCCAGGCAGTTTCCACCCCCTTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:28176969..28177146 26863196 MeRIP-seq:(Medium) rs1230435178 Functional Loss SNV dbSNP153 33..33 33 - - - 65337 RMVar_ID_65337 Human_SNP_ID_641758021 m1A Human chr18 + 28177399 28177399 28177399 AGCGCAGGCGGCTCGGCTCCGGCCCGGAGCGCAGCGGAAGCCGCGAGGGATGCAGCGGCGGGGAC AGCGCAGGCGGCTCGGCTCCGGCCCGGAGCGCCGCGGAAGCCGCGAGGGATGCAGCGGCGGGGAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:28177245..28177535 26863196 MeRIP-seq:(Medium) rs1427429260 Functional Loss SNV dbSNP153 33..33 33 - - - 65338 RMVar_ID_65338 Human_SNP_ID_641758209 m1A Human chr18 + 28177829 28177815 28177829 GCCGCAGCCGCCCCTGCTGCCCGCGCACCGGCACCCGCCCGCCGGTCCTCGCCCTGCGCCGCTCA GCCGCAGCCGCCCCTGCTG______________CCCGCCCGCCGGTCCTCGCCCTGCGCCGCTCA GCCCGCGCACCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:28177778..28177988 26863196 MeRIP-seq:(Medium) rs925046547 Functional Loss DEL dbSNP153 20..33 33 - - - 65339 RMVar_ID_65339 Human_SNP_ID_641758218 m1A Human chr18 + 28177829 28177829 28177829 GCCGCAGCCGCCCCTGCTGCCCGCGCACCGGCACCCGCCCGCCGGTCCTCGCCCTGCGCCGCTCA GCCGCAGCCGCCCCTGCTGCCCGCGCACCGGCCCCCGCCCGCCGGTCCTCGCCCTGCGCCGCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:28177778..28177988 26863196 MeRIP-seq:(Medium) rs183240304 Functional Loss SNV dbSNP153 33..33 33 - - - 65340 RMVar_ID_65340 Human_SNP_ID_641758271 m1A Human chr18 - 28177940 28177940 28177940 AGCCAGGCAGCGCGTGGGGCGAGCGCGGGGAGAGCGGCGGCGGCTCGCCCAGGTCGCGCAGCGGA AGCCAGGCAGCGCGTGGGGCGAGCGCGGGGAGGGCGGCGGCGGCTCGCCCAGGTCGCGCAGCGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:28177216..28178025;chr18:28176951..28178025;chr18:28177756..28178009 26863196 MeRIP-seq:(Medium) rs1346979814 Functional Loss SNV dbSNP153 33..33 33 - - - 65341 RMVar_ID_65341 Human_SNP_ID_208418714 m1A Human chr4 + 150078524 150078524 150078524 GGATCCGGGCGCGGCCGAGGCGGCGGCGCTGCACCCCGGGCCTGGGCCCGCGCGACTCCCCCGGG GGATCCGGGCGCGGCCGAGGCGGCGGCGCTGCGCCCCGGGCCTGGGCCCGCGCGACTCCCCCGGG A G DCLK2 Ensembl:ENSG00000170390 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:150078478..150078551 26863196 MeRIP-seq:(Medium) rs1302746754 Functional Loss SNV dbSNP153 33..33 33 - - - 65342 RMVar_ID_65342 Human_SNP_ID_208461265 m1A Human chr4 + 150249883 150249883 150249883 TTTGGGCACTGTGTGGAGGGGCTTGTGTAGGGACCAGCAGGCCTGGTGTGAGGGGTCCAGGCGTC TTTGGGCACTGTGTGGAGGGGCTTGTGTAGGGTCCAGCAGGCCTGGTGTGAGGGGTCCAGGCGTC A T DCLK2 Ensembl:ENSG00000170390 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:150248351..150253522 32194978 MeRIP-seq:(Medium) rs1028884444 Functional Loss SNV dbSNP153 33..33 33 - - - 65343 RMVar_ID_65343 Human_SNP_ID_208462109 m1A Human chr4 + 150251088 150251088 150251088 TCCCCCACACCACACATCCCTCACACCCCCCAACACCCCCACACACCCCCCACACCACACATCCC TCCCCCACACCACACATCCCTCACACCCCCCACCACCCCCACACACCCCCCACACCACACATCCC A C DCLK2 Ensembl:ENSG00000170390 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:150251044..150251127 26863196 MeRIP-seq:(Medium) rs1483552343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72945,Human_RBP_ID_2823900 65344 RMVar_ID_65344 Human_SNP_ID_208585287 m1A Human chr4 - 150759545 150759545 150759545 GGTATGGTTTGTAGTTTAAATAGAGTGGCAGGATTAGGACTCATTGAGAAAGTAACATTGGAGCA GGTATGGTTTGTAGTTTAAATAGAGTGGCAGGGTTAGGACTCATTGAGAAAGTAACATTGGAGCA T C LRBA Ensembl:ENSG00000198589 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:150759539..150759617 26863196 MeRIP-seq:(Medium) rs918464571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15071010 RMVar_hsa_circ_6511,RMVar_hsa_circ_77517,RMVar_hsa_circ_110120,RMVar_hsa_circ_228994,RMVar_hsa_circ_228995,RMVar_hsa_circ_228997,RMVar_hsa_circ_108345,RMVar_hsa_circ_98011,RMVar_hsa_circ_78367,RMVar_hsa_circ_228999,RMVar_hsa_circ_228998,RMVar_hsa_circ_367047,RMVar_hsa_circ_83830,RMVar_hsa_circ_76447,RMVar_hsa_circ_229004,RMVar_hsa_circ_105855,RMVar_hsa_circ_97503,RMVar_hsa_circ_229005,RMVar_hsa_circ_229006,RMVar_hsa_circ_81290,RMVar_hsa_circ_229008,RMVar_hsa_circ_77540,RMVar_hsa_circ_229009,RMVar_hsa_circ_123679,RMVar_hsa_circ_229007,RMVar_hsa_circ_229014,RMVar_hsa_circ_229016,RMVar_hsa_circ_375238,RMVar_hsa_circ_24819,RMVar_hsa_circ_330007,RMVar_hsa_circ_82364,RMVar_hsa_circ_63015,RMVar_hsa_circ_229020,RMVar_hsa_circ_81083,RMVar_hsa_circ_43120,RMVar_hsa_circ_17537,RMVar_hsa_circ_229021,RMVar_hsa_circ_100752,RMVar_hsa_circ_67220,RMVar_hsa_circ_229025,RMVar_hsa_circ_373314,RMVar_hsa_circ_362720,RMVar_hsa_circ_102893,RMVar_hsa_circ_113104,RMVar_hsa_circ_62662,RMVar_hsa_circ_229029,RMVar_hsa_circ_229030,RMVar_hsa_circ_229028,RMVar_hsa_circ_121753,RMVar_hsa_circ_4500,RMVar_hsa_circ_229032,RMVar_hsa_circ_127442,RMVar_hsa_circ_229031,RMVar_hsa_circ_128081,RMVar_hsa_circ_229033,RMVar_hsa_circ_332971,RMVar_hsa_circ_357270,RMVar_hsa_circ_376125,RMVar_hsa_circ_340163,RMVar_hsa_circ_63885,RMVar_hsa_circ_293531,RMVar_hsa_circ_32714,RMVar_hsa_circ_57343,RMVar_hsa_circ_25292,RMVar_hsa_circ_87963,RMVar_hsa_circ_229034,RMVar_hsa_circ_229035,RMVar_hsa_circ_229039,RMVar_hsa_circ_86468,RMVar_hsa_circ_265621,RMVar_hsa_circ_267994,RMVar_hsa_circ_115571,RMVar_hsa_circ_292355,RMVar_hsa_circ_353167,RMVar_hsa_circ_362907,RMVar_hsa_circ_229040,RMVar_hsa_circ_341261,RMVar_hsa_circ_274068,RMVar_hsa_circ_50519,RMVar_hsa_circ_71099,RMVar_hsa_circ_229045,RMVar_hsa_circ_107496,RMVar_hsa_circ_287798,RMVar_hsa_circ_328705,RMVar_hsa_circ_372489,RMVar_hsa_circ_229041,RMVar_hsa_circ_229042,RMVar_hsa_circ_372764,RMVar_hsa_circ_373840,RMVar_hsa_circ_343495,RMVar_hsa_circ_348257,RMVar_hsa_circ_332864,RMVar_hsa_circ_318803,RMVar_hsa_circ_321611,RMVar_hsa_circ_306105,RMVar_hsa_circ_117643,RMVar_hsa_circ_276170,RMVar_hsa_circ_111659,RMVar_hsa_circ_229049,RMVar_hsa_circ_14219,RMVar_hsa_circ_97303,RMVar_hsa_circ_229051,RMVar_hsa_circ_229053,RMVar_hsa_circ_229054,RMVar_hsa_circ_229052,RMVar_hsa_circ_229050,RMVar_hsa_circ_229047,RMVar_hsa_circ_229048,RMVar_hsa_circ_229046,RMVar_hsa_circ_229043,RMVar_hsa_circ_229044 65345 RMVar_ID_65345 Human_SNP_ID_208632835 m1A Human chr4 - 150952586 150952586 150952586 TTATAGACGGTCAGGATGAGGCTCAGGCAGACATTGACAGACACAGGCAAAGAGACAGGCTCTTG TTATAGACGGTCAGGATGAGGCTCAGGCAGACTTTGACAGACACAGGCAAAGAGACAGGCTCTTG T A LRBA Ensembl:ENSG00000198589 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:150952536..150952751 26863196 MeRIP-seq:(Medium) rs933813407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15072101 RMVar_hsa_circ_373314,RMVar_hsa_circ_229030,RMVar_hsa_circ_10765,RMVar_hsa_circ_35132,RMVar_hsa_circ_104873,RMVar_hsa_circ_229121,RMVar_hsa_circ_113009,RMVar_hsa_circ_229127 65346 RMVar_ID_65346 Human_SNP_ID_208632836 m1A Human chr4 - 150952586 150952586 150952586 TTATAGACGGTCAGGATGAGGCTCAGGCAGACATTGACAGACACAGGCAAAGAGACAGGCTCTTG TTATAGACGGTCAGGATGAGGCTCAGGCAGACCTTGACAGACACAGGCAAAGAGACAGGCTCTTG T G LRBA Ensembl:ENSG00000198589 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:150952536..150952751 26863196 MeRIP-seq:(Medium) rs933813407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15072101 RMVar_hsa_circ_373314,RMVar_hsa_circ_229030,RMVar_hsa_circ_10765,RMVar_hsa_circ_35132,RMVar_hsa_circ_104873,RMVar_hsa_circ_229121,RMVar_hsa_circ_113009,RMVar_hsa_circ_229127 65347 RMVar_ID_65347 Human_SNP_ID_208632900 m1A Human chr4 - 150952732 150952732 150952732 AAAGCACAGATACACATAATTTCAAGAGAGACACACTCAAAGAAGAGATATGCAGATACCAAGAA AAAGCACAGATACACATAATTTCAAGAGAGACCCACTCAAAGAAGAGATATGCAGATACCAAGAA T G LRBA Ensembl:ENSG00000198589 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:150952682..150952780 26863196 MeRIP-seq:(Medium) rs910544461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373314,RMVar_hsa_circ_229030,RMVar_hsa_circ_10765,RMVar_hsa_circ_35132,RMVar_hsa_circ_104873,RMVar_hsa_circ_229121,RMVar_hsa_circ_113009,RMVar_hsa_circ_229127 65348 RMVar_ID_65348 Human_SNP_ID_208669686 m1A Human chr4 + 151099647 151099647 151099647 ACTCCCACTTCCGCCCTTTTGGCTCTCTGACCAGCACCATGGCGGTTGGCAAGAACAAGCGCCTT ACTCCCACTTCCGCCCTTTTGGCTCTCTGACCCGCACCATGGCGGTTGGCAAGAACAAGCGCCTT A C RPS3A Ensembl:ENSG00000145425 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:151099597..151099872 26863196 MeRIP-seq:(Medium) rs759583909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_614992,Human_RBP_ID_4795164,Human_RBP_ID_5326441,Human_RBP_ID_9334814,Human_RBP_ID_26825655 Human_Splice_Rec_615047,Human_Splice_Rec_615059,Human_Splice_Rec_615063,Human_Splice_Rec_615073,Human_Splice_Rec_615095,Human_Splice_Rec_615109,Human_Splice_Rec_615119,Human_Splice_Rec_615129,Human_Splice_Rec_615139 RMVar_hsa_circ_102785,RMVar_hsa_circ_229128 65349 RMVar_ID_65349 Human_SNP_ID_208682075 m1A Human chr4 - 151149551 151149551 151149551 AAGCATTCTCTGCTACTTGCAGGAATCCAACCACCCAGGTCAAACAGGAGGTTTTGTGCGAGTAC AAGCATTCTCTGCTACTTGCAGGAATCCAACCTCCCAGGTCAAACAGGAGGTTTTGTGCGAGTAC T A SH3D19 Ensembl:ENSG00000109686 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:151149407..151149575 26863196 MeRIP-seq:(Medium) rs139493171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941440 Human_Splice_Rec_615178,Human_Splice_Rec_615179,Human_Splice_Rec_615214,Human_Splice_Rec_615215,Human_Splice_Rec_615252,Human_Splice_Rec_615253,Human_Splice_Rec_615278,Human_Splice_Rec_615279,Human_Splice_Rec_615316,Human_Splice_Rec_615317,Human_Splice_Rec_615354,Human_Splice_Rec_615355,Human_Splice_Rec_615396,Human_Splice_Rec_615397,Human_Splice_Rec_615422,Human_Splice_Rec_615423 RMVar_hsa_circ_8448,RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_351514,RMVar_hsa_circ_15610,RMVar_hsa_circ_271310,RMVar_hsa_circ_21530,RMVar_hsa_circ_71263,RMVar_hsa_circ_359458,RMVar_hsa_circ_347761,RMVar_hsa_circ_63822,RMVar_hsa_circ_55424,RMVar_hsa_circ_291423,RMVar_hsa_circ_357810,RMVar_hsa_circ_366899,RMVar_hsa_circ_307919,RMVar_hsa_circ_356172,RMVar_hsa_circ_295594,RMVar_hsa_circ_22006,RMVar_hsa_circ_64392,RMVar_hsa_circ_350295,RMVar_hsa_circ_229135,RMVar_hsa_circ_361606,RMVar_hsa_circ_339701,RMVar_hsa_circ_229137,RMVar_hsa_circ_229138 65350 RMVar_ID_65350 Human_SNP_ID_208706359 m1A Human chr4 - 151251554 151251554 151251554 TAAAGTCAGTAGATTATAAATCCTGATGGAGTAGAAAATTATTGGAATTGGCCTTCTTGCTGTAA TAAAGTCAGTAGATTATAAATCCTGATGGAGTGGAAAATTATTGGAATTGGCCTTCTTGCTGTAA T C SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:151251551..151251855 26863196 MeRIP-seq:(Medium) rs1175038241 Functional Loss SNV dbSNP153 33..33 33 - - - 65351 RMVar_ID_65351 Human_SNP_ID_208706365 m1A Human chr4 - 151251589 151251589 151251589 TAAGCAATGAAGGGGGTGTAGAGAGTAAAGCGAGATAAAGTCAGTAGATTATAAATCCTGATGGA TAAGCAATGAAGGGGGTGTAGAGAGTAAAGCGTGATAAAGTCAGTAGATTATAAATCCTGATGGA T A SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151251587..151251706 26863196 MeRIP-seq:(Medium) rs1421199309 Functional Loss SNV dbSNP153 33..33 33 - - - 65352 RMVar_ID_65352 Human_SNP_ID_208706408 m1A Human chr4 + 151251791 151251791 151251791 CTGAGCAGCACTGGTGAACACACAACTATGCCAATTTCACTTAATTCAAGTGGATCCTTTCAGCT CTGAGCAGCACTGGTGAACACACAACTATGCCGATTTCACTTAATTCAAGTGGATCCTTTCAGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151251789..151251884 26863196 MeRIP-seq:(Medium) rs942995235 Functional Loss SNV dbSNP153 33..33 33 - - - 65353 RMVar_ID_65353 Human_SNP_ID_208716859 m1A Human chr4 - 151293813 151293813 151293813 CATAGAGAATAGGCTGGAAAGTGAGCCAAATGAGGCTGAAGAGACAGGCTGGGGTCAGATTGGCC CATAGAGAATAGGCTGGAAAGTGAGCCAAATGCGGCTGAAGAGACAGGCTGGGGTCAGATTGGCC T G SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:151293811..151293903 26863196 MeRIP-seq:(Medium) rs1326339914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15074151 65354 RMVar_ID_65354 Human_SNP_ID_208743146 m1A Human chr4 - 151405999 151405999 151405999 GGAGAGGCGCATAATTTGAATGTGGGCAGCGTAAGGACGGAACTGCTATAACAAAGTTGGAGAAG GGAGAGGCGCATAATTTGAATGTGGGCAGCGTGAGGACGGAACTGCTATAACAAAGTTGGAGAAG T C FAM160A1-DT,FAM160A1-DT:2,FAM160A1-DT:3,FAM160A1-DT:4,FAM160A1-DT:5,FAM160A1-DT:6,FAM160A1-DT:7,FAM160A1-DT:8,FAM160A1-DT:9,FAM160A1-DT:10 RNACentral:URS0000D57B08,RNACentral:URS0000D5A786,RNACentral:URS0000D5DBA5,RNACentral:URS0000D5DFDC,RNACentral:URS00008C2E90,RNACentral:URS00008BB5B0,RNACentral:URS00008B643B,RNACentral:URS00008BBBCD,RNACentral:URS0000D5B5C9,RNACentral:URS0000D57B1D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,exon,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151405948..151406194 26863196 MeRIP-seq:(Medium) rs1561479660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24040619 65355 RMVar_ID_65355 Human_SNP_ID_208744053 m1A Human chr4 + 151409286 151409286 151409286 CCCGGGCACTCCTGAGTTTGAGCCGGGCCTGGAGGACCTGGGCCAAGACTTTCGAGCGGCGGCCG CCCGGGCACTCCTGAGTTTGAGCCGGGCCTGGGGGACCTGGGCCAAGACTTTCGAGCGGCGGCCG A G FAM160A1 Ensembl:ENSG00000164142 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:151409237..151409374 26863196 MeRIP-seq:(Medium) rs919779160 Functional Loss SNV dbSNP153 33..33 33 - - - 65356 RMVar_ID_65356 Human_SNP_ID_208802256 m1A Human chr4 - 151665544 151665544 151665544 TTGGCATGTCCACGTCACTCCCTAAATAACCCACTCTCAGTTATTTCACCCAGCCACATGGGTTT TTGGCATGTCCACGTCACTCCCTAAATAACCCCCTCTCAGTTATTTCACCCAGCCACATGGGTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151665494..151665623 26863196 MeRIP-seq:(Medium) rs917082331 Functional Loss SNV dbSNP153 33..33 33 - - - 65357 RMVar_ID_65357 Human_SNP_ID_208807253 m1A Human chr4 + 151687228 151687228 151687228 ACTGCAAACCTCCCCAAGATCTTATCAGCTGCAGACTCATAGATCTTGCCTACTGGTTAGCCCCG ACTGCAAACCTCCCCAAGATCTTATCAGCTGCGGACTCATAGATCTTGCCTACTGGTTAGCCCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151687224..151687296 26863196 MeRIP-seq:(Medium) rs1476238518 Functional Loss SNV dbSNP153 33..33 33 - - - 65358 RMVar_ID_65358 Human_SNP_ID_208824254 m1A Human chr4 - 151760921 151760921 151760921 CCGTGGAAGACGTTGGGCTTTCGCCCGGGTTGACGGTGGTTCTTGCCACCGAAGAGGGGCTCCGA CCGTGGAAGACGTTGGGCTTTCGCCCGGGTTGGCGGTGGTTCTTGCCACCGAAGAGGGGCTCCGA T C GATB Ensembl:ENSG00000059691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:151760871..151760942 26863196 MeRIP-seq:(Medium) rs1560870298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795165,Human_RBP_ID_9396741 65359 RMVar_ID_65359 Human_SNP_ID_208824276 m1A Human chr4 - 151760946 151760946 151760946 CGGCGCCCATGCTGCGCTGGGGCTGCCGTGGAAGACGTTGGGCTTTCGCCCGGGTTGACGGTGGT CGGCGCCCATGCTGCGCTGGGGCTGCCGTGGAGGACGTTGGGCTTTCGCCCGGGTTGACGGTGGT T C GATB Ensembl:ENSG00000059691 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:151760870..151760963 26863196 MeRIP-seq:(Medium) rs367564064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786864,Human_RBP_ID_4795669,Human_RBP_ID_9396741 65360 RMVar_ID_65360 Human_SNP_ID_208824277 m1A Human chr4 - 151760947 151760947 151760947 GCGGCGCCCATGCTGCGCTGGGGCTGCCGTGGAAGACGTTGGGCTTTCGCCCGGGTTGACGGTGG GCGGCGCCCATGCTGCGCTGGGGCTGCCGTGGTAGACGTTGGGCTTTCGCCCGGGTTGACGGTGG T A GATB Ensembl:ENSG00000059691 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151760777..151760959 26863196 MeRIP-seq:(Medium) rs772678895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786864,Human_RBP_ID_4795669,Human_RBP_ID_9396741 65361 RMVar_ID_65361 Human_SNP_ID_208981500 m1A Human chr4 - 152411528 152411528 152411528 AATAGATTTATTTCGGTAGATGAGGACTCCTCAGGAAACCAAGAAGAACAAGAGGAAGATGAAGA AATAGATTTATTTCGGTAGATGAGGACTCCTCGGGAAACCAAGAAGAACAAGAGGAAGATGAAGA T C FBXW7 Ensembl:ENSG00000109670 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:152411388..152411569 26863196 MeRIP-seq:(Medium) rs527954747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213549,Human_RBP_ID_1641629,Human_RBP_ID_2825513,Human_RBP_ID_9396744,Human_RBP_ID_15076233,Human_RBP_ID_18536945,Human_RBP_ID_22095713,Human_RBP_ID_24547737,Human_RBP_ID_26349628,Human_RBP_ID_27824488 RMVar_hsa_circ_229164,RMVar_hsa_circ_124066,RMVar_hsa_circ_229157,RMVar_hsa_circ_54029,RMVar_hsa_circ_112966,RMVar_hsa_circ_72425,RMVar_hsa_circ_289038,RMVar_hsa_circ_284630,RMVar_hsa_circ_272402,RMVar_hsa_circ_282171,RMVar_hsa_circ_122878,RMVar_hsa_circ_229166,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168,RMVar_hsa_circ_229165 65362 RMVar_ID_65362 Human_SNP_ID_208981541 m1A Human chr4 - 152411666 152411666 152411666 GTGGTAGAGGAGGAACAGCAACAGCAACTCAGACAACAAGAGGAGGAGCACACTGCAAGGAATGG GTGGTAGAGGAGGAACAGCAACAGCAACTCAGTCAACAAGAGGAGGAGCACACTGCAAGGAATGG T A FBXW7 Ensembl:ENSG00000109670 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:152411616..152411709 26863196 MeRIP-seq:(Medium) rs1472384625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12195,Human_RBP_ID_248896,Human_RBP_ID_18536946,Human_RBP_ID_26349630 RMVar_hsa_circ_229164,RMVar_hsa_circ_124066,RMVar_hsa_circ_229157,RMVar_hsa_circ_54029,RMVar_hsa_circ_112966,RMVar_hsa_circ_72425,RMVar_hsa_circ_289038,RMVar_hsa_circ_284630,RMVar_hsa_circ_272402,RMVar_hsa_circ_282171,RMVar_hsa_circ_122878,RMVar_hsa_circ_229166,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168,RMVar_hsa_circ_229165 65363 RMVar_ID_65363 Human_SNP_ID_208981542 m1A Human chr4 - 152411666 152411666 152411666 GTGGTAGAGGAGGAACAGCAACAGCAACTCAGACAACAAGAGGAGGAGCACACTGCAAGGAATGG GTGGTAGAGGAGGAACAGCAACAGCAACTCAGGCAACAAGAGGAGGAGCACACTGCAAGGAATGG T C FBXW7 Ensembl:ENSG00000109670 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:152411616..152411709 26863196 MeRIP-seq:(Medium) rs1472384625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12195,Human_RBP_ID_248896,Human_RBP_ID_18536946,Human_RBP_ID_26349630 RMVar_hsa_circ_229164,RMVar_hsa_circ_124066,RMVar_hsa_circ_229157,RMVar_hsa_circ_54029,RMVar_hsa_circ_112966,RMVar_hsa_circ_72425,RMVar_hsa_circ_289038,RMVar_hsa_circ_284630,RMVar_hsa_circ_272402,RMVar_hsa_circ_282171,RMVar_hsa_circ_122878,RMVar_hsa_circ_229166,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168,RMVar_hsa_circ_229165 65364 RMVar_ID_65364 Human_SNP_ID_209011645 m1A Human chr4 + 152535716 152535716 152535716 GGTCTCGCCCCACGCCCCACGGGACGAGGCAGAAGCTCTGGCGCCTCCTCAGCGTTCTCTCACCG GGTCTCGCCCCACGCCCCACGGGACGAGGCAGGAGCTCTGGCGCCTCCTCAGCGTTCTCTCACCG A G MIR4453HG RNACentral:URS00008B82E8 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:152535666..152536065 26863196 MeRIP-seq:(Medium) rs1346129148 Functional Loss SNV dbSNP153 33..33 33 - - - 65365 RMVar_ID_65365 Human_SNP_ID_209011646 m1A Human chr4 + 152535717 152535717 152535717 GTCTCGCCCCACGCCCCACGGGACGAGGCAGAAGCTCTGGCGCCTCCTCAGCGTTCTCTCACCGC GTCTCGCCCCACGCCCCACGGGACGAGGCAGACGCTCTGGCGCCTCCTCAGCGTTCTCTCACCGC A C MIR4453HG RNACentral:URS00008B82E8 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:152535666..152536050 26863196 MeRIP-seq:(Medium) rs1285658483 Functional Loss SNV dbSNP153 33..33 33 - - - 65366 RMVar_ID_65366 Human_SNP_ID_209011706 m1A Human chr4 - 152535827 152535827 152535827 GCTGCACACGCCGGAGCCGGAGCCAGAGCCGGAGCCCGAGCCTGAGCCGGAGCCGGCGGCTTGGG GCTGCACACGCCGGAGCCGGAGCCAGAGCCGGCGCCCGAGCCTGAGCCGGAGCCGGCGGCTTGGG T G FBXW7 Ensembl:ENSG00000109670 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:152535780..152535907 26863196 MeRIP-seq:(Medium) rs898859035 Functional Loss SNV dbSNP153 33..33 33 - - - 65367 RMVar_ID_65367 Human_SNP_ID_209011732 m1A Human chr4 - 152535852 152535852 152535852 CTCACCTTCCCGGCCGGCAGCGGCGGCTGCACACGCCGGAGCCGGAGCCAGAGCCGGAGCCCGAG CTCACCTTCCCGGCCGGCAGCGGCGGCTGCACGCGCCGGAGCCGGAGCCAGAGCCGGAGCCCGAG T C FBXW7 Ensembl:ENSG00000109670 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:152535563..152535982 26863196 MeRIP-seq:(Medium) rs1417413408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9397481 65368 RMVar_ID_65368 Human_SNP_ID_209011848 m1A Human chr4 + 152536042 152536042 152536042 GGCGGCAGCGGCAGCGGCAGCGCCCGGAGCTCAGCTCGCTGTCTCCCTCGCTCTGTGCGGGGCTC GGCGGCAGCGGCAGCGGCAGCGCCCGGAGCTCGGCTCGCTGTCTCCCTCGCTCTGTGCGGGGCTC A G MIR4453HG RNACentral:URS00008B82E8 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:152535602..152536066 26863196 MeRIP-seq:(Medium) rs1014405576 Functional Loss SNV dbSNP153 33..33 33 - - - 65369 RMVar_ID_65369 Human_SNP_ID_209012021 m1A Human chr4 + 152536339 152536339 152536339 GACTCGCAGCCGCCACCGCCGCTGCCGCCTCTACGGCCGCGTCAGAACTGAAGAGAGGAAGGGGA GACTCGCAGCCGCCACCGCCGCTGCCGCCTCTCCGGCCGCGTCAGAACTGAAGAGAGGAAGGGGA A C MIR4453HG Ensembl:ENSG00000268471 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:152536296..152536397 26863196 MeRIP-seq:(Medium) rs1056440986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4775740 65370 RMVar_ID_65370 Human_SNP_ID_209012024 m1A Human chr4 - 152536355 152536355 152536355 GGCTCGACTCGGCTCCTCCCCTTCCTCTCTTCAGTTCTGACGCGGCCGTAGAGGCGGCAGCGGCG GGCTCGACTCGGCTCCTCCCCTTCCTCTCTTCGGTTCTGACGCGGCCGTAGAGGCGGCAGCGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:152536305..152536550 26863196 MeRIP-seq:(Medium) rs1313593212 Functional Loss SNV dbSNP153 33..33 33 - - - 65371 RMVar_ID_65371 Human_SNP_ID_209012025 m1A Human chr4 - 152536355 152536355 152536355 GGCTCGACTCGGCTCCTCCCCTTCCTCTCTTCAGTTCTGACGCGGCCGTAGAGGCGGCAGCGGCG GGCTCGACTCGGCTCCTCCCCTTCCTCTCTTCCGTTCTGACGCGGCCGTAGAGGCGGCAGCGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:152536305..152536550 26863196 MeRIP-seq:(Medium) rs1313593212 Functional Loss SNV dbSNP153 33..33 33 - - - 65372 RMVar_ID_65372 Human_SNP_ID_209088228 m1A Human chr4 - 152855262 152855262 152855262 CTTCCCCACCCCCCGCAGCTGTGCCAGAACACATAGTCTGGGGGCCACAGCATTGCCCAGCCCAG CTTCCCCACCCCCCGCAGCTGTGCCAGAACACGTAGTCTGGGGGCCACAGCATTGCCCAGCCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:152855261..152855344 26863196 MeRIP-seq:(Medium) rs573672024 Functional Loss SNV dbSNP153 33..33 33 - - - 65373 RMVar_ID_65373 Human_SNP_ID_209181085 m1A Human chr4 + 153231399 153231399 153231399 ATCAAGGATAATATAATTGAGGAAGAGGGACTAAAGTTAGAACTTAAAGAATGTGCAAGATTTAG ATCAAGGATAATATAATTGAGGAAGAGGGACTGAAGTTAGAACTTAAAGAATGTGCAAGATTTAG A G TRIM2 Ensembl:ENSG00000109654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:153231391..153231531 26863196 MeRIP-seq:(Medium) rs558176859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15078916 65374 RMVar_ID_65374 Human_SNP_ID_209208335 m1A Human chr4 + 153344738 153344738 153344738 GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCATGGTAAGGACTGAGGCTACGGTCCCGCGTCTT GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCCTGGTAAGGACTGAGGCTACGGTCCCGCGTCTT A C MND1 Ensembl:ENSG00000121211 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153344673..153344795 26863196 MeRIP-seq:(Medium) rs750080695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795166,Human_RBP_ID_18424821,Human_RBP_ID_19121868 Human_Splice_Rec_616341,Human_Splice_Rec_616353,Human_Splice_Rec_616357,Human_Splice_Rec_616375 65375 RMVar_ID_65375 Human_SNP_ID_209208336 m1A Human chr4 + 153344738 153344738 153344738 GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCATGGTAAGGACTGAGGCTACGGTCCCGCGTCTT GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCTTGGTAAGGACTGAGGCTACGGTCCCGCGTCTT A T MND1 Ensembl:ENSG00000121211 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153344673..153344795 26863196 MeRIP-seq:(Medium) rs750080695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795166,Human_RBP_ID_18424821,Human_RBP_ID_19121868 Human_Splice_Rec_616341,Human_Splice_Rec_616353,Human_Splice_Rec_616357,Human_Splice_Rec_616375 65376 RMVar_ID_65376 Human_SNP_ID_209208337 m1A Human chr4 - 153344739 153344739 153344739 GAAGACGCGGGACCGTAGCCTCAGTCCTTACCATGGCGCGGGCGCAGGGGCTTCCGCTGGCCGGG GAAGACGCGGGACCGTAGCCTCAGTCCTTACCGTGGCGCGGGCGCAGGGGCTTCCGCTGGCCGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:153344716..153344788;chr4:153344705..153344805;chr4:153344665..153344809 26863196 MeRIP-seq:(Medium) rs983018953 Functional Loss SNV dbSNP153 33..33 33 - - - 65377 RMVar_ID_65377 Human_SNP_ID_209209081 m1A Human chr4 + 153348008 153348008 153348008 GGAGCCACTGGAGGGTTTTGAGCAAGGCAGGGAAAAAGGTCTTATTTATGTTTTCCCAGTGCGGA GGAGCCACTGGAGGGTTTTGAGCAAGGCAGGGGAAAAGGTCTTATTTATGTTTTCCCAGTGCGGA A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:153348006..153348146 26863196 MeRIP-seq:(Medium) rs1389729664 Functional Loss SNV dbSNP153 33..33 33 - - - 65378 RMVar_ID_65378 Human_SNP_ID_209209135 m1A Human chr4 + 153348316 153348309 153348316 TCAAGGTCTAGAACAGCAAGTTTGTGGGGAGTAGGTATGAGAGAGGAAGAGTTCAGTTTAGACTG TCAAGGTCTAGAACAGCAAGTTTGTG_______GGTATGAGAGAGGAAGAGTTCAGTTTAGACTG GGGGAGTA G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153348310..153348403 26863196 MeRIP-seq:(Medium) rs1471562850 Functional Loss DEL dbSNP153 27..33 33 - - - 65379 RMVar_ID_65379 Human_SNP_ID_209219078 m1A Human chr4 + 153389054 153389053 153389055 GAGTATGCAAAGAAAGACTAAAGGCACCACTCAGAGGTGAGCACAGCAATATAGAAAACCAATTA GAGTATGCAAAGAAAGACTAAAGGCACCACTC__AGGTGAGCACAGCAATATAGAAAACCAATTA CAG C MND1 Ensembl:ENSG00000121211 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:153389038..153389130 26863196 MeRIP-seq:(Medium) rs1376787928 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_322851,RMVar_hsa_circ_303155,RMVar_hsa_circ_229216,RMVar_hsa_circ_229215,RMVar_hsa_circ_229218,RMVar_hsa_circ_84076 65380 RMVar_ID_65380 Human_SNP_ID_209243924 m1A Human chr4 + 153487791 153487789 153487791 CTGAGCTGTATGTGTGTGTGTGGGAGTGTGCGAGAGAGAGGAGCCAGGGACAAGGAGAGAGACCC CTGAGCTGTATGTGTGTGTGTGGGAGTGTGC__GAGAGAGGAGCCAGGGACAAGGAGAGAGACCC CGA C TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:153487753..153488369 26863196 MeRIP-seq:(Medium) rs1434462053 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11965,Human_RBP_ID_785872,Human_RBP_ID_5300961,Human_RBP_ID_5655119,Human_RBP_ID_17296419,Human_RBP_ID_24041692 RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 65381 RMVar_ID_65381 Human_SNP_ID_209245996 m1A Human chr4 + 153495415 153495415 153495415 CCTCAGGAGGTCCTGTGCCCAGGGTGGTCGGGATACAGCTTGCTTTTATATATTTTAGGGAGACA CCTCAGGAGGTCCTGTGCCCAGGGTGGTCGGGCTACAGCTTGCTTTTATATATTTTAGGGAGACA A C TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153495407..153495489 26863196 MeRIP-seq:(Medium) rs1292910871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 65382 RMVar_ID_65382 Human_SNP_ID_209257480 m1A Human chr4 + 153542120 153542120 153542120 CTACAGTGATCACAAATGTCAGTGAAGGAAGCATTAATCTGTGGGTGATAGGCAAACCCACTGGA CTACAGTGATCACAAATGTCAGTGAAGGAAGCGTTAATCTGTGGGTGATAGGCAAACCCACTGGA A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153542110..153542198 26863196 MeRIP-seq:(Medium) rs1042778055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 65383 RMVar_ID_65383 Human_SNP_ID_209266256 m1A Human chr4 + 153577224 153577224 153577224 AGTGAGGTTGGAGCATGCGCAGGGAGGTCGAGACTAGGCAGGTGCCGGAGTTTTATAGCGACAGC AGTGAGGTTGGAGCATGCGCAGGGAGGTCGAGGCTAGGCAGGTGCCGGAGTTTTATAGCGACAGC A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153577175..153577244 26863196 MeRIP-seq:(Medium) rs986553478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15080803 RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_56652,RMVar_hsa_circ_377488 65384 RMVar_ID_65384 Human_SNP_ID_209266411 m1A Human chr4 - 153577832 153577832 153577832 ACCCCAACCTGGCCACCTTTGCTGTGTGCCTCATCTTAGCACCATTATTCATCAACCCTATCATT ACCCCAACCTGGCCACCTTTGCTGTGTGCCTCGTCTTAGCACCATTATTCATCAACCCTATCATT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:153577807..153578036;chr4:153577792..153577909 26863196 MeRIP-seq:(Medium) rs769496067 Functional Loss SNV dbSNP153 33..33 33 - - - 65385 RMVar_ID_65385 Human_SNP_ID_209266466 m1A Human chr4 + 153578024 153578024 153578024 CATAGGCAGCATCCAGCATAACTCAGTGTCTGATGGTTAAAGGAGCAACAGCTGGCAGAGGAACC CATAGGCAGCATCCAGCATAACTCAGTGTCTGGTGGTTAAAGGAGCAACAGCTGGCAGAGGAACC A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:153577975..153578199 26863196 MeRIP-seq:(Medium) rs1268964190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15080808 RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_56652,RMVar_hsa_circ_377488 65386 RMVar_ID_65386 Human_SNP_ID_209499827 m1A Human chr4 - 154535964 154535964 154535964 ACAAAGAAGGAAAAGAGATGAGGCATAAAGTGATGAAACCAGGCACAAGAAAGTGTGCGGTGTGT ACAAAGAAGGAAAAGAGATGAGGCATAAAGTGGTGAAACCAGGCACAAGAAAGTGTGCGGTGTGT T C PLRG1 Ensembl:ENSG00000171566 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:154535913..154536005 26863196 MeRIP-seq:(Medium) rs957755245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15081301 65387 RMVar_ID_65387 Human_SNP_ID_209499830 m1A Human chr4 - 154535976 154535976 154535976 AAGTGAAGGAAGACAAAGAAGGAAAAGAGATGAGGCATAAAGTGATGAAACCAGGCACAAGAAAG AAGTGAAGGAAGACAAAGAAGGAAAAGAGATGCGGCATAAAGTGATGAAACCAGGCACAAGAAAG T G PLRG1 Ensembl:ENSG00000171566 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:154535926..154536023 26863196 MeRIP-seq:(Medium) rs749527087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15081301 65388 RMVar_ID_65388 Human_SNP_ID_209502949 m1A Human chr4 + 154548918 154548918 154548918 CTCTTCAACGACCTGAACACAAGGGTGTGTACAGAATGTTTCTGTACCTCCTAAAAAAAAAGAAT CTCTTCAACGACCTGAACACAAGGGTGTGTACGGAATGTTTCTGTACCTCCTAAAAAAAAAGAAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:154548868..154549086 26863196 MeRIP-seq:(Medium) rs551201192 Functional Loss SNV dbSNP153 33..33 33 - - - 65389 RMVar_ID_65389 Human_SNP_ID_209502954 m1A Human chr4 - 154548934 154548934 154548934 ATAGGTGTGTAATTACATTCTTTTTTTTTAGGAGGTACAGAAACATTCTGTACACACCCTTGTGT ATAGGTGTGTAATTACATTCTTTTTTTTTAGGTGGTACAGAAACATTCTGTACACACCCTTGTGT T A PLRG1 Ensembl:ENSG00000171566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:154548887..154548973 26863196 MeRIP-seq:(Medium) rs773088495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12196,Human_RBP_ID_249590,Human_RBP_ID_939806,Human_RBP_ID_7281417,Human_RBP_ID_22679438,Human_RBP_ID_23213914,Human_RBP_ID_27825139 Human_Splice_Rec_616892,Human_Splice_Rec_616938,Human_Splice_Rec_616968,Human_Splice_Rec_616988,Human_Splice_Rec_617002,Human_Splice_Rec_617012,Human_Splice_Rec_617020,Human_Splice_Rec_617026 RMVar_hsa_circ_79405,RMVar_hsa_circ_70192,RMVar_hsa_circ_229271 65390 RMVar_ID_65390 Human_SNP_ID_209726126 m1A Human chr4 + 155464493 155464493 155464493 AAAAGTAAGAGACAGCTGAACCCTCGTGTAGCAATTCGTACAAGTCCCTATTTAGGGAACAAGTG AAAAGTAAGAGACAGCTGAACCCTCGTGTAGCCATTCGTACAAGTCCCTATTTAGGGAACAAGTG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr4:155464356..155464646;chr4:155464406..155464556 26863196 MeRIP-seq:(Medium) rs1368620680 Functional Loss SNV dbSNP153 33..33 33 - - - 65391 RMVar_ID_65391 Human_SNP_ID_210105395 m1A Human chr4 - 156971630 156971630 156971630 GAGCCCGAACAAGGTGAACTTTGGTCGCGGAAAACTCAAGCCAGGTGCCGGAATCCGTGCTGCGG GAGCCCGAACAAGGTGAACTTTGGTCGCGGAAGACTCAAGCCAGGTGCCGGAATCCGTGCTGCGG T C PDGFC Ensembl:ENSG00000145431 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:156971561..156971732 26863196 MeRIP-seq:(Medium) rs904757798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5426146,Human_RBP_ID_5475256,Human_RBP_ID_18820178 65392 RMVar_ID_65392 Human_SNP_ID_210414876 m1A Human chr4 + 158210502 158210502 158210502 AGGCCGCCCCCAGCACGTAGAGGGAATGAGTCAGGCTCCGGCTCCACACTGGCACGTAGTGGGCG AGGCCGCCCCCAGCACGTAGAGGGAATGAGTCGGGCTCCGGCTCCACACTGGCACGTAGTGGGCG A G TMEM144 Ensembl:ENSG00000164124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:158210451..158210528 26863196 MeRIP-seq:(Medium) rs900515010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_618853,Human_Splice_Rec_618867,Human_Splice_Rec_618877,Human_Splice_Rec_618885,Human_Splice_Rec_618899,Human_Splice_Rec_618901,Human_Splice_Rec_618905,Human_Splice_Rec_618913,Human_Splice_Rec_618937 65393 RMVar_ID_65393 Human_SNP_ID_210523571 m1A Human chr4 + 158672336 158672336 158672336 AGAGCGGTCGGCAGAGCGGGGAGGCGAACTGCAGCAGAGTTCTTGCTTTCCGGCAGGTGATGGCG AGAGCGGTCGGCAGAGCGGGGAGGCGAACTGCGGCAGAGTTCTTGCTTTCCGGCAGGTGATGGCG A G ETFDH Ensembl:ENSG00000171503 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:158672151..158672433 26863196 MeRIP-seq:(Medium) rs1259368875 Functional Loss SNV dbSNP153 33..33 33 - - - 65394 RMVar_ID_65394 Human_SNP_ID_210534466 m1A Human chr4 - 158717199 158717199 158717199 CTTGGTTTTCTTTTAATTTTTATTTCTACAGCATGATCGGGAGGGTTTACTGAGCATGGCAAATG CTTGGTTTTCTTTTAATTTTTATTTCTACAGCGTGATCGGGAGGGTTTACTGAGCATGGCAAATG T C PPID Ensembl:ENSG00000171497 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:158717151..158717200 26863196 MeRIP-seq:(Medium) rs772525566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7282911,Human_RBP_ID_15083783,Human_RBP_ID_24042665,Human_RBP_ID_25829910 Human_Splice_Rec_619390 RMVar_hsa_circ_64863,RMVar_hsa_circ_75278 65395 RMVar_ID_65395 Human_SNP_ID_210536162 m1A Human chr4 - 158723326 158723326 158723326 TGGAGTTTGGGCGGCCCGGGCGGCCACTAGGTACTCTGATATTCCGTACTAAACACGTCTGCAAG TGGAGTTTGGGCGGCCCGGGCGGCCACTAGGTGCTCTGATATTCCGTACTAAACACGTCTGCAAG T C PPID Ensembl:ENSG00000171497 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:158723275..158723362 26863196 MeRIP-seq:(Medium) rs1320848960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_615699,Human_RBP_ID_787141,Human_RBP_ID_4795171,Human_RBP_ID_18424643,Human_RBP_ID_24042674,Human_RBP_ID_27063711 65396 RMVar_ID_65396 Human_SNP_ID_210547301 m1A Human chr4 - 158769156 158769130 158769157 GTGGCGCTCGGGGGGCCGGCGGCTCAGCGCGCAGCCGGGGGCGGCGGCCGCGGTGGCGGGGCCAT GTGGCGCTCGGGGGGCCGGCGGCTCAGCGCG___________________________GGGCCAT CCGCCACCGCGGCCGCCGCCCCCGGCTG C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:158769073..158769227 26863410 MeRIP-seq:(Medium) rs1446155955 Functional Loss DEL dbSNP153 32..58 33 - - - 65397 RMVar_ID_65397 Human_SNP_ID_210625349 m1A Human chr4 - 159104150 159104150 159104150 TTATCTACGTAGGACGCCATCTCCCCTCTGGGAGCGGGCCGGGGCCGCTCCGCACCCTGGCCGGC TTATCTACGTAGGACGCCATCTCCCCTCTGGGCGCGGGCCGGGGCCGCTCCGCACCCTGGCCGGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:159104101..159104214 26863196 MeRIP-seq:(Medium) rs1292272996 Functional Loss SNV dbSNP153 33..33 33 - - - 65398 RMVar_ID_65398 Human_SNP_ID_210657050 m1A Human chr4 + 159228291 159228291 159228291 AAATGGGGAGTGCTCAGTGCTGCAGAGAAAAGAGCTCCTATAGAAGGTGACAGCACTGTTGGTGT AAATGGGGAGTGCTCAGTGCTGCAGAGAAAAGGGCTCCTATAGAAGGTGACAGCACTGTTGGTGT A G RAPGEF2 Ensembl:ENSG00000109756 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:159228194..159228398 26863196 MeRIP-seq:(Medium) rs1561111574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_619595 RMVar_hsa_circ_28181,RMVar_hsa_circ_39471,RMVar_hsa_circ_338944,RMVar_hsa_circ_301380,RMVar_hsa_circ_72132,RMVar_hsa_circ_229355,RMVar_hsa_circ_34894,RMVar_hsa_circ_351749,RMVar_hsa_circ_299252 65399 RMVar_ID_65399 Human_SNP_ID_210666555 m1A Human chr4 + 159266163 159266163 159266163 TGGGGCAGAGGTTAAGCATATGTGGCAAAAGAAGGATAATGGGTAATGTAAGAAAAGGGGTTGGG TGGGGCAGAGGTTAAGCATATGTGGCAAAAGACGGATAATGGGTAATGTAAGAAAAGGGGTTGGG A C RAPGEF2 Ensembl:ENSG00000109756 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:159266050..159266328 26863196 MeRIP-seq:(Medium) rs893841777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28181,RMVar_hsa_circ_39471,RMVar_hsa_circ_338944,RMVar_hsa_circ_72132,RMVar_hsa_circ_34894,RMVar_hsa_circ_278896,RMVar_hsa_circ_318352,RMVar_hsa_circ_229357 65400 RMVar_ID_65400 Human_SNP_ID_211554818 m1A Human chr4 + 162712294 162712294 162712294 TGCCTATCCACCCTGTGGTGCCCAACCCGTACACTCTTTCATCCTCAATACCTTCCTCCACAACT TGCCTATCCACCCTGTGGTGCCCAACCCGTACTCTCTTTCATCCTCAATACCTTCCTCCACAACT A T AC021134.1 Ensembl:ENSG00000248431 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:162712261..162712349 26863196 MeRIP-seq:(Medium) rs544603862 Functional Loss SNV dbSNP153 33..33 33 - - - 65401 RMVar_ID_65401 Human_SNP_ID_211663452 m1A Human chr4 - 163161906 163161903 163161907 AGGGTGGGAGTGCGTAACAGCCAGTTGACAGAAAGGGAGTGTGAATGTGTATGTATTGTGAGGAG AGGGTGGGAGTGCGTAACAGCCAGTTGACAG____GGAGTGTGAATGTGTATGTATTGTGAGGAG CCTTT C NAF1 Ensembl:ENSG00000145414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:163161899..163162020 26863196 MeRIP-seq:(Medium) rs1366450619 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_70983,RMVar_hsa_circ_376659 65402 RMVar_ID_65402 Human_SNP_ID_211664573 m1A Human chr4 - 163166378 163166378 163166378 GGCGCCGGACTCCTTGGAGACCTCGGACTCGGATTCGGACTCGGACAGGTCGGGTGCCTAAGGGA GGCGCCGGACTCCTTGGAGACCTCGGACTCGGGTTCGGACTCGGACAGGTCGGGTGCCTAAGGGA T C NAF1 Ensembl:ENSG00000145414 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:163166375..163166772 32194978 MeRIP-seq:(Medium) rs1173616911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1636148,Human_RBP_ID_8878005 Human_Splice_Rec_619903,Human_Splice_Rec_619917,Human_Splice_Rec_619933,Human_Splice_Rec_619945 65403 RMVar_ID_65403 Human_SNP_ID_211664814 m1A Human chr4 + 163166806 163166806 163166806 ACAAGCTCACGGCTCTCTCCAGAAATAGAAAAACAACTTAGGCAACCGCAGCAACACTGCCTGGG ACAAGCTCACGGCTCTCTCCAGAAATAGAAAAGCAACTTAGGCAACCGCAGCAACACTGCCTGGG A G NONHSAG039245.2 RNACentral:URS00008B77B4 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:163166660..163166843;chr4:163166635..163166829 26863196 MeRIP-seq:(Medium) rs1305615656 Functional Loss SNV dbSNP153 33..33 33 - - - 65404 RMVar_ID_65404 Human_SNP_ID_211743964 m1A Human chr4 - 163494719 163494719 163494719 TCTCACCAACCGCAGGAGCAGCAGCTCACAAGAGCACCCGGGCCGAATCCCACGTGGCGCCTGAG TCTCACCAACCGCAGGAGCAGCAGCTCACAAGCGCACCCGGGCCGAATCCCACGTGGCGCCTGAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:163494676..163494824;chr4:163494678..163494827 26863196 MeRIP-seq:(Medium) rs561867134 Functional Loss SNV dbSNP153 33..33 33 - - - 65405 RMVar_ID_65405 Human_SNP_ID_211743977 m1A Human chr4 - 163494752 163494752 163494752 CACGGAGCAGCTCCGCACTCTAGACCCAGGTAATCTCACCAACCGCAGGAGCAGCAGCTCACAAG CACGGAGCAGCTCCGCACTCTAGACCCAGGTAGTCTCACCAACCGCAGGAGCAGCAGCTCACAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:163494701..163512460 32194978 MeRIP-seq:(Medium) rs748485743 Functional Loss SNV dbSNP153 33..33 33 - - - 65406 RMVar_ID_65406 Human_SNP_ID_211743994 m1A Human chr4 - 163494776 163494776 163494776 CCACCATGGTGACGTCCTCGTGGCCACGGAGCAGCTCCGCACTCTAGACCCAGGTAATCTCACCA CCACCATGGTGACGTCCTCGTGGCCACGGAGCGGCTCCGCACTCTAGACCCAGGTAATCTCACCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:163494726..163494825 32194978 MeRIP-seq:(Medium) rs1278163232 Functional Loss SNV dbSNP153 33..33 33 - - - 65407 RMVar_ID_65407 Human_SNP_ID_211743995 m1A Human chr4 - 163494776 163494776 163494776 CCACCATGGTGACGTCCTCGTGGCCACGGAGCAGCTCCGCACTCTAGACCCAGGTAATCTCACCA CCACCATGGTGACGTCCTCGTGGCCACGGAGCCGCTCCGCACTCTAGACCCAGGTAATCTCACCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:163494726..163494825 32194978 MeRIP-seq:(Medium) rs1278163232 Functional Loss SNV dbSNP153 33..33 33 - - - 65408 RMVar_ID_65408 Human_SNP_ID_211748736 m1A Human chr4 + 163515419 163515419 163515419 GGCACTGTTCCCGGGAGACCGTCATCAAGCAGACGATGGAGCGGGAGCGACAGCAGTTTGAGGGA GGCACTGTTCCCGGGAGACCGTCATCAAGCAGGCGATGGAGCGGGAGCGACAGCAGTTTGAGGGA A G TMA16 Ensembl:ENSG00000198498 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:163515301..163515521 32194978 MeRIP-seq:(Medium) rs1321382706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249227,Human_RBP_ID_838137,Human_RBP_ID_7284747,Human_RBP_ID_9396774,Human_RBP_ID_27824507 Human_Splice_Rec_620001,Human_Splice_Rec_620047,Human_Splice_Rec_620059,Human_Splice_Rec_620065 RMVar_hsa_circ_126267,RMVar_hsa_circ_229395 65409 RMVar_ID_65409 Human_SNP_ID_211920993 m1A Human chr4 - 164196971 164196971 164196971 CCTGAAGATGAGGGAGAAGATGATGACTAAGTAGAATAACCTATTTTGAAAAATTCCTATTGTGA CCTGAAGATGAGGGAGAAGATGATGACTAAGTGGAATAACCTATTTTGAAAAATTCCTATTGTGA T C MARCHF1 Ensembl:ENSG00000145416 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1484609627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17408 65410 RMVar_ID_65410 Human_SNP_ID_211921044 m1A Human chr4 - 164197088 164197086 164197089 GACGTGAGTGGAGGGGACGAGGAGGATGAAGAAGGTTATAACGATGGAGAGGTAGATGGCGAGGA GACGTGAGTGGAGGGGACGAGGAGGATGAAG___GTTATAACGATGGAGAGGTAGATGGCGAGGA CCTT C MARCHF1,ANP32C Ensembl:ENSG00000145416,Ensembl:ENSG00000248546 Protein coding,Pseudogene intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:164197049..164197169 26863196 MeRIP-seq:(Medium) rs771384935 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1035648 RMVar_hsa_circ_17408 65411 RMVar_ID_65411 Human_SNP_ID_568553758 m1A Human chr14 + 105010940 105010937 105010941 CGGCTCACCGTCCTCTACAGTGGGGGACACAAAGAGACACGAGGGGCCCAGGGCTGTGGGGACGT CGGCTCACCGTCCTCTACAGTGGGGGACAC____AGACACGAGGGGCCCAGGGCTGTGGGGACGT CAAAG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:105010826..105010950 32194978 MeRIP-seq:(Medium) rs560987283 Functional Loss DEL dbSNP153 31..34 33 - - - 65412 RMVar_ID_65412 Human_SNP_ID_568556748 m1A Human chr14 + 105021044 105021044 105021044 CCGCCCGCCGGGTCCTCTGCTCAGCCACCGCCACCGCCGCTGCCGCCAGCTTCCCGCCGCTGAGG CCGCCCGCCGGGTCCTCTGCTCAGCCACCGCCCCCGCCGCTGCCGCCAGCTTCCCGCCGCTGAGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105020822..105021100;chr14:105020922..105021075 26863196 MeRIP-seq:(Medium) rs1566940900 Functional Loss SNV dbSNP153 33..33 33 - - - 65413 RMVar_ID_65413 Human_SNP_ID_568573557 m1A Human chr14 + 105082794 105082794 105082794 CCATCTACCCATCCATCCATCTCTATCCTTCGATCCCTCTATCCATCCATCCATCCCCCATCAAC CCATCTACCCATCCATCCATCTCTATCCTTCGCTCCCTCTATCCATCCATCCATCCCCCATCAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105082587..105083176 26863196 MeRIP-seq:(Medium) rs1272275423 Functional Loss SNV dbSNP153 33..33 33 - - - 65414 RMVar_ID_65414 Human_SNP_ID_568573761 m1A Human chr14 - 105083290 105083286 105083290 GGAGGGGTGAATAGAGGAGTGGAAGGGCAGATAGAGGGATTGATGGATGTGTGGATAGAGAGATG GGAGGGGTGAATAGAGGAGTGGAAGGGCAGAT____GGATTGATGGATGTGTGGATAGAGAGATG CCTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105083258..105083424 26863196 MeRIP-seq:(Medium) rs1201118230 Functional Loss DEL dbSNP153 33..36 33 - - - 65415 RMVar_ID_65415 Human_SNP_ID_568574021 m1A Human chr14 + 105083906 105083906 105083906 TATCTGCCCTTCCACTCCTCTATTCACCATCCACCCATCCATCTCTATCCATTCATCCCTGTATC TATCTGCCCTTCCACTCCTCTATTCACCATCCGCCCATCCATCTCTATCCATTCATCCCTGTATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105083857..105084021 26863196 MeRIP-seq:(Medium) rs1041411564 Functional Loss SNV dbSNP153 33..33 33 - - - 65416 RMVar_ID_65416 Human_SNP_ID_568574029 m1A Human chr14 - 105083976 105083972 105083976 TGGATGGAGAGGTGGATACAGGAATGGATAGAAGGATGGATGGATGGATGAATAGAGGAGTGGGT TGGATGGAGAGGTGGATACAGGAATGGATAGA____TGGATGGATGGATGAATAGAGGAGTGGGT ATCCT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105083848..105084283 26863196 MeRIP-seq:(Medium) rs1168070519 Functional Loss DEL dbSNP153 33..36 33 - - - 65417 RMVar_ID_65417 Human_SNP_ID_568574868 m1A Human chr14 - 105087206 105087206 105087206 GCCCATTTCCCTGCCTGGGAAACAAAGGCCCCAGGTCTGCAGTGCGTCTGATGGCGGGGAGGAGA GCCCATTTCCCTGCCTGGGAAACAAAGGCCCCGGGTCTGCAGTGCGTCTGATGGCGGGGAGGAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105087131..105087418 26863196 MeRIP-seq:(Medium) rs1299560839 Functional Loss SNV dbSNP153 33..33 33 - - - 65418 RMVar_ID_65418 Human_SNP_ID_568576695 m1A Human chr14 - 105093637 105093637 105093637 CCCTGGGGTTACAGCCGGCGGAGGGGCTTCCCAAAAGAATCCTCAGCCTCTCCCGCCTGCGGCGG CCCTGGGGTTACAGCCGGCGGAGGGGCTTCCCGAAAGAATCCTCAGCCTCTCCCGCCTGCGGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105093589..105093702 26863196 MeRIP-seq:(Medium) rs1261754587 Functional Loss SNV dbSNP153 33..33 33 - - - 65419 RMVar_ID_65419 Human_SNP_ID_568588855 m1A Human chr14 + 105142053 105142053 105142053 CGGCAGGCAGGGTGGACTGGCCAGCAAGCGCGAGGTTGACCTGCCAGCCTTGGGCCACGCCGATG CGGCAGGCAGGGTGGACTGGCCAGCAAGCGCGTGGTTGACCTGCCAGCCTTGGGCCACGCCGATG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105142012..105142255 26863196 MeRIP-seq:(Medium) rs960840745 Functional Loss SNV dbSNP153 33..33 33 - - - 65420 RMVar_ID_65420 Human_SNP_ID_568589197 m1A Human chr14 + 105142918 105142918 105142918 CCCTGACGGCCGCGTGGCCGGCCGGCCCGGGCAGCGCCTCGTCCGCCCTGCGCGGCGGCGGCGTG CCCTGACGGCCGCGTGGCCGGCCGGCCCGGGCTGCGCCTCGTCCGCCCTGCGCGGCGGCGGCGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105142868..105142957 26863196 MeRIP-seq:(Medium) rs1231803834 Functional Loss SNV dbSNP153 33..33 33 - - - 65421 RMVar_ID_65421 Human_SNP_ID_568592296 m1A Human chr14 + 105150611 105150611 105150611 GGCAGGGTGACCAGGCAGACCTCACCTCACAGAGAGGCCCGGAGAAGCCCTGGGGGCAGTGGCAG GGCAGGGTGACCAGGCAGACCTCACCTCACAGCGAGGCCCGGAGAAGCCCTGGGGGCAGTGGCAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105148992..105150756 32194978 MeRIP-seq:(Medium) rs1334971589 Functional Loss SNV dbSNP153 33..33 33 - - - 65422 RMVar_ID_65422 Human_SNP_ID_568593752 m1A Human chr14 - 105154646 105154646 105154646 GAAAGTGGGGAAGGCAGAGAGGAGGGAGGCCAAGGAGCAAGTCCCGGCTGCCACAGGTCAGGGCG GAAAGTGGGGAAGGCAGAGAGGAGGGAGGCCAGGGAGCAAGTCCCGGCTGCCACAGGTCAGGGCG T C JAG2,AL512356.1 Ensembl:ENSG00000184916,Ensembl:ENSG00000257622 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105154631..105154724 26863196 MeRIP-seq:(Medium) rs1207394084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9417982 RMVar_hsa_circ_88714,RMVar_hsa_circ_169686,RMVar_hsa_circ_79286,RMVar_hsa_circ_169687 65423 RMVar_ID_65423 Human_SNP_ID_568594136 m1A Human chr14 - 105155771 105155771 105155771 ACACCTGCGACCAGTACGGCAACAAGGCCTGCATGGACGGCTGGATGGGCAAGGAGTGCAAGGAA ACACCTGCGACCAGTACGGCAACAAGGCCTGCGTGGACGGCTGGATGGGCAAGGAGTGCAAGGAA T C JAG2,AL512356.1 Ensembl:ENSG00000184916,Ensembl:ENSG00000257622 Protein coding,lincRNA CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105155606..105155932 26863196 MeRIP-seq:(Medium) rs143241003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442309,Human_RBP_ID_4285055,Human_RBP_ID_5565255 Human_Splice_Rec_1561267,Human_Splice_Rec_1561315,Human_Splice_Rec_1561379,Human_Splice_Rec_1561391 RMVar_hsa_circ_88714,RMVar_hsa_circ_169686,RMVar_hsa_circ_79286,RMVar_hsa_circ_169687,RMVar_hsa_circ_11581,RMVar_hsa_circ_376381,RMVar_hsa_circ_169689 65424 RMVar_ID_65424 Human_SNP_ID_568598615 m1A Human chr14 - 105168641 105168618 105168641 GAGCCGGGCCGGGCAGCCGGAGCGCGGCCGCCAGCGAGCCGGAGCTGCCGCCGCCCCTGCACGCC GAGCCGGGCCGGGCAGCCGGAGCGCGGCCGCC_______________________CCTGCACGCC GGGCGGCGGCAGCTCCGGCTCGCT G JAG2,AL512356.1 Ensembl:ENSG00000184916,Ensembl:ENSG00000257622 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105168602..105168745 26863196 MeRIP-seq:(Medium) rs938847782 Functional Loss DEL dbSNP153 33..55 33 - - - 65425 RMVar_ID_65425 Human_SNP_ID_568598625 m1A Human chr14 - 105168653 105168653 105168653 GCCGCCGGGTGGGAGCCGGGCCGGGCAGCCGGAGCGCGGCCGCCAGCGAGCCGGAGCTGCCGCCG GCCGCCGGGTGGGAGCCGGGCCGGGCAGCCGGGGCGCGGCCGCCAGCGAGCCGGAGCTGCCGCCG T C JAG2,AL512356.1 Ensembl:ENSG00000184916,Ensembl:ENSG00000257622 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,untreat control chr14:105168526..105168736;chr14:105168581..105168718;chr14:105168554..105168725 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1291932183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3470260,Human_RBP_ID_5315988 65426 RMVar_ID_65426 Human_SNP_ID_568599966 m1A Human chr14 - 105173142 105173142 105173142 GGTGGAGGAGGGTGAGCTCATTGAGGTGGTGCACCTGCCCCTGGAAGGCGCCCAGGCCTTTGCAG GGTGGAGGAGGGTGAGCTCATTGAGGTGGTGCCCCTGCCCCTGGAAGGCGCCCAGGCCTTTGCAG T G NUDT14,AL512356.1 Ensembl:ENSG00000183828,Ensembl:ENSG00000257622 Protein coding,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105173092..105173158 26863196 MeRIP-seq:(Medium) rs1370661431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112819 RMVar_hsa_circ_87793,RMVar_hsa_circ_93436,RMVar_hsa_circ_89731,RMVar_hsa_circ_169691,RMVar_hsa_circ_169693,RMVar_hsa_circ_80283,RMVar_hsa_circ_169692,RMVar_hsa_circ_169690 65427 RMVar_ID_65427 Human_SNP_ID_568600011 m1A Human chr14 - 105173263 105173263 105173263 TGGGTGACTCAGCAGACCCTGTCTCAACCCGTAGGTCTGGAGTGGGACTGACTGGCTCCAGACAG TGGGTGACTCAGCAGACCCTGTCTCAACCCGTGGGTCTGGAGTGGGACTGACTGGCTCCAGACAG T C NUDT14,AL512356.1 Ensembl:ENSG00000183828,Ensembl:ENSG00000257622 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105173233..105173314 26863196 MeRIP-seq:(Medium) rs368648959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442314,Human_RBP_ID_3467904,Human_RBP_ID_4310596,Human_RBP_ID_5315990,Human_RBP_ID_5351542,Human_RBP_ID_9324173,Human_RBP_ID_21969648 RMVar_hsa_circ_87793,RMVar_hsa_circ_89731,RMVar_hsa_circ_169691,RMVar_hsa_circ_80283,RMVar_hsa_circ_169692,RMVar_hsa_circ_169690 65428 RMVar_ID_65428 Human_SNP_ID_568600060 m1A Human chr14 + 105173379 105173379 105173379 TCCACTCTGCTCCCTCCAGCCCTCCAGTAGGCAGGACTCTGGGATGCCCTCTCCCACCCGGATTC TCCACTCTGCTCCCTCCAGCCCTCCAGTAGGCGGGACTCTGGGATGCCCTCTCCCACCCGGATTC A G NONHSAG016091.2 RNACentral:URS00008B8063 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105173376..105173484 26863196 MeRIP-seq:(Medium) rs1383620032 Functional Loss SNV dbSNP153 33..33 33 - - - 65429 RMVar_ID_65429 Human_SNP_ID_568600384 m1A Human chr14 - 105174536 105174536 105174536 GGGTAAGGTCGGTCTGGGGTGAGTCCCCCCGGAGGTGGGGAGGCCTTGGGGGTGGGGCATGGAAG GGGTAAGGTCGGTCTGGGGTGAGTCCCCCCGGGGGTGGGGAGGCCTTGGGGGTGGGGCATGGAAG T C NUDT14,AL512356.1 Ensembl:ENSG00000183828,Ensembl:ENSG00000257622 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105174382..105174768 26863196 MeRIP-seq:(Medium) rs748659051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812806,Human_RBP_ID_3469470,Human_RBP_ID_5095456 RMVar_hsa_circ_87793,RMVar_hsa_circ_89731,RMVar_hsa_circ_169691,RMVar_hsa_circ_80283,RMVar_hsa_circ_169692,RMVar_hsa_circ_169690 65430 RMVar_ID_65430 Human_SNP_ID_568602368 m1A Human chr14 + 105181176 105181176 105181176 CGTGAGCGGCCGCAGGTAGGGTGAGGCGGCGCAGCGGCCCACGGACGCCCCCTCGATGCGCTCCA CGTGAGCGGCCGCAGGTAGGGTGAGGCGGCGCTGCGGCCCACGGACGCCCCCTCGATGCGCTCCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105177755..105181278 26863196 MeRIP-seq:(Medium) rs1453444788 Functional Loss SNV dbSNP153 33..33 33 - - - 65431 RMVar_ID_65431 Human_SNP_ID_568602425 m1A Human chr14 + 105181256 105181256 105181256 AGGCGGGGGCCGCGAGCTCTGCGGGGGCCGACACGGGGCGGCGCCCTGTCCCGACAGGAGCCTTC AGGCGGGGGCCGCGAGCTCTGCGGGGGCCGACGCGGGGCGGCGCCCTGTCCCGACAGGAGCCTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105181160..105181261 26863196 MeRIP-seq:(Medium) rs1216264245 Functional Loss SNV dbSNP153 33..33 33 - - - 65432 RMVar_ID_65432 Human_SNP_ID_568602437 m1A Human chr14 - 105181270 105181270 105181270 TCACGCGCCCGCCCGAAGGCTCCTGTCGGGACAGGGCGCCGCCCCGTGTCGGCCCCCGCAGAGCT TCACGCGCCCGCCCGAAGGCTCCTGTCGGGACCGGGCGCCGCCCCGTGTCGGCCCCCGCAGAGCT T G NUDT14 Ensembl:ENSG00000183828 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105181164..105181274 26863196 MeRIP-seq:(Medium) rs992469255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4309137 65433 RMVar_ID_65433 Human_SNP_ID_568611848 m1A Human chr14 + 105211177 105211177 105211177 GCACTGACGCAGGGCTCCCCGTCCTCCTCGTCAGGCTCCTCCTCGTCAGCCTCCTCGTCGGCGTG GCACTGACGCAGGGCTCCCCGTCCTCCTCGTCCGGCTCCTCCTCGTCAGCCTCCTCGTCGGCGTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105210432..105211764 26863196 MeRIP-seq:(Medium) rs1008540253 Functional Loss SNV dbSNP153 33..33 33 - - - 65434 RMVar_ID_65434 Human_SNP_ID_568617352 m1A Human chr14 - 105226135 105226135 105226135 CTTCAGGTGAAATATCCAGTTACCAGGATGCAATTGAGATTGAACTAGAAAACAGCCGGCCAAAG CTTCAGGTGAAATATCCAGTTACCAGGATGCAGTTGAGATTGAACTAGAAAACAGCCGGCCAAAG T C BRF1 Ensembl:ENSG00000185024 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105226086..105226276 26863196 MeRIP-seq:(Medium) rs1479121773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_881170,Human_RBP_ID_5353517,Human_RBP_ID_9369575,Human_RBP_ID_12287431,Human_RBP_ID_18646764,Human_RBP_ID_27809219 Human_Splice_Rec_1561440,Human_Splice_Rec_1561441,Human_Splice_Rec_1561472,Human_Splice_Rec_1561473,Human_Splice_Rec_1561506,Human_Splice_Rec_1561507,Human_Splice_Rec_1561554,Human_Splice_Rec_1561555,Human_Splice_Rec_1561580,Human_Splice_Rec_1561604,Human_Splice_Rec_1561626,Human_Splice_Rec_1561627,Human_Splice_Rec_1561660,Human_Splice_Rec_1561661,Human_Splice_Rec_1561688,Human_Splice_Rec_1561689,Human_Splice_Rec_1561712,Human_Splice_Rec_1561713,Human_Splice_Rec_1561724,Human_Splice_Rec_1561725,Human_Splice_Rec_1561738 Human_miRNA_ID_2231172,Human_miRNA_ID_2231173 RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_108620,RMVar_hsa_circ_169696,RMVar_hsa_circ_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_169700,RMVar_hsa_circ_265061,RMVar_hsa_circ_281834,RMVar_hsa_circ_305011,RMVar_hsa_circ_313005,RMVar_hsa_circ_287213,RMVar_hsa_circ_169701 65435 RMVar_ID_65435 Human_SNP_ID_568617616 m1A Human chr14 - 105226708 105226708 105226708 CCCCCACCAGTCAGTTGACCATTGATGAGTTCATGAAGATCGACCTGGAGGAGGAGTGCGACCCC CCCCCACCAGTCAGTTGACCATTGATGAGTTCTTGAAGATCGACCTGGAGGAGGAGTGCGACCCC T A BRF1 Ensembl:ENSG00000185024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105226593..105226720 26863196 MeRIP-seq:(Medium) rs1180120530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120585,Human_RBP_ID_882342,Human_RBP_ID_9369576,Human_RBP_ID_26325555,Human_RBP_ID_27808638 Human_Splice_Rec_1561436,Human_Splice_Rec_1561437,Human_Splice_Rec_1561468,Human_Splice_Rec_1561469,Human_Splice_Rec_1561502,Human_Splice_Rec_1561503,Human_Splice_Rec_1561550,Human_Splice_Rec_1561551,Human_Splice_Rec_1561576,Human_Splice_Rec_1561577,Human_Splice_Rec_1561586,Human_Splice_Rec_1561600,Human_Splice_Rec_1561601,Human_Splice_Rec_1561622,Human_Splice_Rec_1561623,Human_Splice_Rec_1561656,Human_Splice_Rec_1561657,Human_Splice_Rec_1561685,Human_Splice_Rec_1561708,Human_Splice_Rec_1561709,Human_Splice_Rec_1561720,Human_Splice_Rec_1561721,Human_Splice_Rec_1561734,Human_Splice_Rec_1561735 RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_108620,RMVar_hsa_circ_169696,RMVar_hsa_circ_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_169700,RMVar_hsa_circ_281834,RMVar_hsa_circ_305011,RMVar_hsa_circ_313005,RMVar_hsa_circ_287213,RMVar_hsa_circ_169701,RMVar_hsa_circ_121477,RMVar_hsa_circ_78092,RMVar_hsa_circ_169702,RMVar_hsa_circ_169703 65436 RMVar_ID_65436 Human_SNP_ID_568623427 m1A Human chr14 - 105248713 105248713 105248713 CGCGGCCGTGCAGGCAGGCTAGGGGCAGCAGCATGGGCGGCGGCGGCGCTGTGACCCGCGGGGCT CGCGGCCGTGCAGGCAGGCTAGGGGCAGCAGCGTGGGCGGCGGCGGCGCTGTGACCCGCGGGGCT T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105248576..105249200 26863196 MeRIP-seq:(Medium) rs1428242319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_108620,RMVar_hsa_circ_169696,RMVar_hsa_circ_50010,RMVar_hsa_circ_305011,RMVar_hsa_circ_121477,RMVar_hsa_circ_97507,RMVar_hsa_circ_169703,RMVar_hsa_circ_169704,RMVar_hsa_circ_265922 65437 RMVar_ID_65437 Human_SNP_ID_568623533 m1A Human chr14 + 105248990 105248984 105248990 GGGCCGCGCAGCCCGCCCAGCGCCCCCGCGCCAGCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC GGGCCGCGCAGCCCGCCCAGCGCCCCC______GCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC CGCGCCA C BTBD6 Ensembl:ENSG00000184887 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:105248635..105249139 26863410 MeRIP-seq:(Medium) rs1455203229 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_231316 Human_Splice_Rec_1561759,Human_Splice_Rec_1561767,Human_Splice_Rec_1561773,Human_Splice_Rec_1561783 RMVar_hsa_circ_114110,RMVar_hsa_circ_94676,RMVar_hsa_circ_169705,RMVar_hsa_circ_169706 65438 RMVar_ID_65438 Human_SNP_ID_568623538 m1A Human chr14 + 105248990 105248990 105248990 GGGCCGCGCAGCCCGCCCAGCGCCCCCGCGCCAGCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC GGGCCGCGCAGCCCGCCCAGCGCCCCCGCGCCCGCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC A C BTBD6 Ensembl:ENSG00000184887 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:105248635..105249139 26863410 MeRIP-seq:(Medium) rs2816604 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_231316 Human_Splice_Rec_1561759,Human_Splice_Rec_1561767,Human_Splice_Rec_1561773,Human_Splice_Rec_1561783 RMVar_hsa_circ_114110,RMVar_hsa_circ_94676,RMVar_hsa_circ_169705,RMVar_hsa_circ_169706 65439 RMVar_ID_65439 Human_SNP_ID_568623570 m1A Human chr14 + 105249033 105249033 105249033 CGCCCGCGCCCGCGCCGCCCACACTCGGCAACAACCACCAGGAGAGCCCCGGCTGGCGGTGCTGC CGCCCGCGCCCGCGCCGCCCACACTCGGCAACCACCACCAGGAGAGCCCCGGCTGGCGGTGCTGC A C BTBD6 Ensembl:ENSG00000184887 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:105248939..105249039 26863410 MeRIP-seq:(Medium) rs587629356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231316 Human_Splice_Rec_1561759,Human_Splice_Rec_1561767,Human_Splice_Rec_1561773,Human_Splice_Rec_1561783 RMVar_hsa_circ_114110,RMVar_hsa_circ_94676,RMVar_hsa_circ_169705,RMVar_hsa_circ_169706 65440 RMVar_ID_65440 Human_SNP_ID_568635054 m1A Human chr14 - 105290783 105290783 105290783 GTGTTGGGGGACAGGGAGAACAACACAGGGACAGGAAACAGAGGTCCTGGGGTGTGAGGAGGGTA GTGTTGGGGGACAGGGAGAACAACACAGGGACGGGAAACAGAGGTCCTGGGGTGTGAGGAGGGTA T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105290780..105290867 26863196 MeRIP-seq:(Medium) rs764586935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_96431,RMVar_hsa_circ_169710 65441 RMVar_ID_65441 Human_SNP_ID_568637902 m1A Human chr14 - 105300596 105300596 105300596 TGACGGGCCGCGTGTGCCGCGGTTGCGGCGGCACGGACATCGAGCTGGACGCGGCGCGCGGGGAC TGACGGGCCGCGTGTGCCGCGGTTGCGGCGGCGCGGACATCGAGCTGGACGCGGCGCGCGGGGAC T C BRF1 Ensembl:ENSG00000185024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105300548..105300962 26863196 MeRIP-seq:(Medium) rs587752262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_96431,RMVar_hsa_circ_169710 65442 RMVar_ID_65442 Human_SNP_ID_568656766 m1A Human chr14 - 105364444 105364444 105364444 GCACCCGGGACGCCGCCCACCGCGCACCCGGGACGCCGCCCACCGCGCACCCGGGACACCGCCCA GCACCCGGGACGCCGCCCACCGCGCACCCGGGCCGCCGCCCACCGCGCACCCGGGACACCGCCCA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:105364347..105364539 26863196 MeRIP-seq:(Medium) rs1238197081 Functional Loss SNV dbSNP153 33..33 33 - - - 65443 RMVar_ID_65443 Human_SNP_ID_568656808 m1A Human chr14 - 105364516 105364493 105364516 CAAGCCTGGATGGTGCCGCCCACCGCGCACCCAGGCCACCGCCCACCGCGCACCCGGGCCGCCAC CAAGCCTGGATGGTGCCGCCCACCGCGCACCC_______________________GGGCCGCCAC CGGGTGCGCGGTGGGCGGTGGCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105364205..105364596 26863196 MeRIP-seq:(Medium) rs1555407494 Functional Loss DEL dbSNP153 33..55 33 - - - 65444 RMVar_ID_65444 Human_SNP_ID_568656814 m1A Human chr14 - 105364516 105364501 105364517 CAAGCCTGGATGGTGCCGCCCACCGCGCACCCAGGCCACCGCCCACCGCGCACCCGGGCCGCCAC CAAGCCTGGATGGTGCCGCCCACCGCGCACC________________GCGCACCCGGGCCGCCAC CGGTGGGCGGTGGCCTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105364205..105364596 26863196 MeRIP-seq:(Medium) rs1269887223 Functional Loss DEL dbSNP153 32..47 33 - - - 65445 RMVar_ID_65445 Human_SNP_ID_568656827 m1A Human chr14 - 105364516 105364516 105364516 CAAGCCTGGATGGTGCCGCCCACCGCGCACCCAGGCCACCGCCCACCGCGCACCCGGGCCGCCAC CAAGCCTGGATGGTGCCGCCCACCGCGCACCCGGGCCACCGCCCACCGCGCACCCGGGCCGCCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105364205..105364596 26863196 MeRIP-seq:(Medium) rs587627737 Functional Loss SNV dbSNP153 33..33 33 - - - 65446 RMVar_ID_65446 Human_SNP_ID_568657567 m1A Human chr14 + 105367261 105367261 105367261 CTGAAGGTGGCCAGGTGCTGAGCCTCTGCAGCAGCATCAAGGAGGCCCCCGTCAAGGCGGCCGAG CTGAAGGTGGCCAGGTGCTGAGCCTCTGCAGCTGCATCAAGGAGGCCCCCGTCAAGGCGGCCGAG A T PACS2 Ensembl:ENSG00000179364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105355175..105367310 32194978 MeRIP-seq:(Medium) rs1555408165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1561798,Human_Splice_Rec_1561844,Human_Splice_Rec_1561890,Human_Splice_Rec_1561936,Human_Splice_Rec_1561984,Human_Splice_Rec_1561986 RMVar_hsa_circ_90970,RMVar_hsa_circ_41918,RMVar_hsa_circ_377088,RMVar_hsa_circ_377947,RMVar_hsa_circ_285492,RMVar_hsa_circ_124251,RMVar_hsa_circ_169715,RMVar_hsa_circ_34822,RMVar_hsa_circ_169717,RMVar_hsa_circ_123227,RMVar_hsa_circ_294549,RMVar_hsa_circ_169718,RMVar_hsa_circ_169719 65447 RMVar_ID_65447 Human_SNP_ID_568664797 m1A Human chr14 + 105390943 105390925 105390944 AGCGTCCTGTTTTTACTGCACACATAGTTTGCAGCTGCCCTGAGGGCCGACTTTAGAGAGAGCAG AGCGTCCTGTTTTTA___________________CTGCCCTGAGGGCCGACTTTAGAGAGAGCAG ACTGCACACATAGTTTGCAG A PACS2 Ensembl:ENSG00000179364 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105390939..105391339 32194978 MeRIP-seq:(Medium) rs1555414645 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_18646821 RMVar_hsa_circ_104475,RMVar_hsa_circ_121080,RMVar_hsa_circ_169723,RMVar_hsa_circ_169724 65448 RMVar_ID_65448 Human_SNP_ID_568664979 m1A Human chr14 + 105391525 105391525 105391525 CTCACAGGCCACTGGGGACTCCCACCCTGCCCACCCCCAGGAGCTGCCTGGCCTGGCCACATCCT CTCACAGGCCACTGGGGACTCCCACCCTGCCCCCCCCCAGGAGCTGCCTGGCCTGGCCACATCCT A C PACS2 Ensembl:ENSG00000179364 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105391487..105391688 32194978 MeRIP-seq:(Medium) rs1204796181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22415096,Human_RBP_ID_22648924 Human_Splice_Rec_1562060 RMVar_hsa_circ_104475,RMVar_hsa_circ_121080,RMVar_hsa_circ_169723,RMVar_hsa_circ_169724 65449 RMVar_ID_65449 Human_SNP_ID_568667394 m1A Human chr14 - 105398595 105398595 105398595 GATGGAGAGGCCACAGGGGGCCGCTGGAGTACACCGCGGCTTGAGGGGGCCCAAGGGGCCGGCGC GATGGAGAGGCCACAGGGGGCCGCTGGAGTACCCCGCGGCTTGAGGGGGCCCAAGGGGCCGGCGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105398582..105398732 26863196 MeRIP-seq:(Medium) rs1555417938 Functional Loss SNV dbSNP153 33..33 33 - - - 65450 RMVar_ID_65450 Human_SNP_ID_568667676 m1A Human chr14 - 105399305 105399305 105399305 TAGCCCTAGTAGGCTGCTTGTCCACACCTCTGAGATCTGGGGGTAGGAGCAGGGGGAGGTGGGGC TAGCCCTAGTAGGCTGCTTGTCCACACCTCTGGGATCTGGGGGTAGGAGCAGGGGGAGGTGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105399300..105399424 26863196 MeRIP-seq:(Medium) rs1311374486 Functional Loss SNV dbSNP153 33..33 33 - - - 65451 RMVar_ID_65451 Human_SNP_ID_568671514 m1A Human chr14 - 105412562 105412562 105412562 CTCAGCACCCTTCCGAGGGCCCTGCAGCCTGGAAACGAGGCAGTCACCCAGTGGACCATGTCCCA CTCAGCACCCTTCCGAGGGCCCTGCAGCCTGGTAACGAGGCAGTCACCCAGTGGACCATGTCCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105412559..105412644 26863196 MeRIP-seq:(Medium) rs1298713609 Functional Loss SNV dbSNP153 33..33 33 - - - 65452 RMVar_ID_65452 Human_SNP_ID_568673501 m1A Human chr14 + 105420036 105420036 105420036 CCCCGGGCCCCTCCGCCGCCGCCGGCCCGGACATGGCCGCCAACATGTACAGGGTCGGAGGTAAG CCCCGGGCCCCTCCGCCGCCGCCGGCCCGGACGTGGCCGCCAACATGTACAGGGTCGGAGGTAAG A G MTA1,TEX22 Ensembl:ENSG00000182979,Ensembl:ENSG00000226174 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:105419851..105420100 26863410 MeRIP-seq:(Medium) rs1555420447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4285516,Human_RBP_ID_18189461,Human_RBP_ID_18435626 Human_Splice_Rec_1562103,Human_Splice_Rec_1562145,Human_Splice_Rec_1562185,Human_Splice_Rec_1562223,Human_Splice_Rec_1562261,Human_Splice_Rec_1562301 65453 RMVar_ID_65453 Human_SNP_ID_568678459 m1A Human chr14 + 105438721 105438721 105438721 AACTCCTCCAGCAACCCATACCTGATCCGGAGAATCGAGGAGCTCAACAAGGTACTGGGGGGCCC AACTCCTCCAGCAACCCATACCTGATCCGGAGGATCGAGGAGCTCAACAAGGTACTGGGGGGCCC A G MTA1,TEX22 Ensembl:ENSG00000182979,Ensembl:ENSG00000226174 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr14:105438651..105438725;chr14:105438651..105438750 26863196 MeRIP-seq:(Medium) rs1555424979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1171291,Human_RBP_ID_1489905,Human_RBP_ID_1815809,Human_RBP_ID_3944749,Human_RBP_ID_4310666,Human_RBP_ID_6329550,Human_RBP_ID_8400877,Human_RBP_ID_12288812,Human_RBP_ID_18646898,Human_RBP_ID_18981180 Human_Splice_Rec_1562082,Human_Splice_Rec_1562083,Human_Splice_Rec_1562104,Human_Splice_Rec_1562105,Human_Splice_Rec_1562146,Human_Splice_Rec_1562147,Human_Splice_Rec_1562186,Human_Splice_Rec_1562187,Human_Splice_Rec_1562224,Human_Splice_Rec_1562225,Human_Splice_Rec_1562262,Human_Splice_Rec_1562263,Human_Splice_Rec_1562302,Human_Splice_Rec_1562303,Human_Splice_Rec_1562311,Human_Splice_Rec_1562325 RMVar_hsa_circ_14003,RMVar_hsa_circ_333657,RMVar_hsa_circ_373421,RMVar_hsa_circ_315519,RMVar_hsa_circ_327477,RMVar_hsa_circ_39157,RMVar_hsa_circ_169728,RMVar_hsa_circ_169729 65454 RMVar_ID_65454 Human_SNP_ID_568679530 m1A Human chr14 - 105441876 105441876 105441876 GATGGATCCCATCCATTTCTCAGAGAACATTCACGGGCTTTGTTTTGCTTTAGTTTCCTTCTGTT GATGGATCCCATCCATTTCTCAGAGAACATTCGCGGGCTTTGTTTTGCTTTAGTTTCCTTCTGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105441870..105442111 26863196 MeRIP-seq:(Medium) rs973958813 Functional Loss SNV dbSNP153 33..33 33 - - - 65455 RMVar_ID_65455 Human_SNP_ID_568680560 m1A Human chr14 - 105445402 105445402 105445402 ACGTTCCCATTGGCCGTCTGTAACAGCAAGGCAGGGGCGTCTGAGAAACGCGACCAAACCCGGGC ACGTTCCCATTGGCCGTCTGTAACAGCAAGGCGGGGGCGTCTGAGAAACGCGACCAAACCCGGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105445401..105445500 26863196 MeRIP-seq:(Medium) rs147590251 Functional Loss SNV dbSNP153 33..33 33 - - - 65456 RMVar_ID_65456 Human_SNP_ID_568680561 m1A Human chr14 - 105445402 105445402 105445402 ACGTTCCCATTGGCCGTCTGTAACAGCAAGGCAGGGGCGTCTGAGAAACGCGACCAAACCCGGGC ACGTTCCCATTGGCCGTCTGTAACAGCAAGGCCGGGGCGTCTGAGAAACGCGACCAAACCCGGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105445401..105445500 26863196 MeRIP-seq:(Medium) rs147590251 Functional Loss SNV dbSNP153 33..33 33 - - - 65457 RMVar_ID_65457 Human_SNP_ID_568680993 m1A Human chr14 + 105447032 105447032 105447032 AAGGAGGAGAGCTGGGGATGTTGAAGGTCCACAGGCTACACATTCTGGAGGGGTGTTTGGTGTGG AAGGAGGAGAGCTGGGGATGTTGAAGGTCCACGGGCTACACATTCTGGAGGGGTGTTTGGTGTGG A G MTA1,TEX22 Ensembl:ENSG00000182979,Ensembl:ENSG00000226174 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:105447029..105447241 26863196 MeRIP-seq:(Medium) rs974100446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442414,Human_RBP_ID_1490010,Human_RBP_ID_17651276,Human_RBP_ID_22737430 RMVar_hsa_circ_14003,RMVar_hsa_circ_333657,RMVar_hsa_circ_373421,RMVar_hsa_circ_315519,RMVar_hsa_circ_39157,RMVar_hsa_circ_169729,RMVar_hsa_circ_318660,RMVar_hsa_circ_370714,RMVar_hsa_circ_326271,RMVar_hsa_circ_10523,RMVar_hsa_circ_169731,RMVar_hsa_circ_169732,RMVar_hsa_circ_169730 65458 RMVar_ID_65458 Human_SNP_ID_568685906 m1A Human chr14 + 105464093 105464093 105464093 TCAACAACGTCAAGGCCGGTGTGGTGAACGGCACGGGGGCGCCGGGCCAGAGCCCTGGGGCTGGC TCAACAACGTCAAGGCCGGTGTGGTGAACGGCGCGGGGGCGCCGGGCCAGAGCCCTGGGGCTGGC A G MTA1 Ensembl:ENSG00000182979 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:105464051..105464150 26863196 MeRIP-seq:(Medium) rs782355369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_997728,Human_RBP_ID_3944753,Human_RBP_ID_17248722 Human_Splice_Rec_1562126,Human_Splice_Rec_1562127,Human_Splice_Rec_1562168,Human_Splice_Rec_1562169,Human_Splice_Rec_1562208,Human_Splice_Rec_1562209,Human_Splice_Rec_1562244,Human_Splice_Rec_1562245,Human_Splice_Rec_1562284,Human_Splice_Rec_1562285,Human_Splice_Rec_1562374,Human_Splice_Rec_1562375,Human_Splice_Rec_1562398,Human_Splice_Rec_1562399,Human_Splice_Rec_1562406,Human_Splice_Rec_1562407,Human_Splice_Rec_1562412,Human_Splice_Rec_1562413,Human_Splice_Rec_1562415 RMVar_hsa_circ_12078,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_32655,RMVar_hsa_circ_29116,RMVar_hsa_circ_326011 65459 RMVar_ID_65459 Human_SNP_ID_568686816 m1A Human chr14 - 105466399 105466399 105466399 GGGTCTCTGCCGGGAATGACACAGGCAGAACGAGTTGCCTCTGCCCAGCAGGGGAGGGGCAGGCA GGGTCTCTGCCGGGAATGACACAGGCAGAACGGGTTGCCTCTGCCCAGCAGGGGAGGGGCAGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105466396..105466530 26863196 MeRIP-seq:(Medium) rs782150710 Functional Loss SNV dbSNP153 33..33 33 - - - 65460 RMVar_ID_65460 Human_SNP_ID_568688192 m1A Human chr14 + 105470124 105470124 105470124 GGAAACCAAGCGTGCTGCCCGCCGGCCCTACAAGCCCATCGCCCTGCGCCAGAGCCAGGCCCTGC GGAAACCAAGCGTGCTGCCCGCCGGCCCTACAGGCCCATCGCCCTGCGCCAGAGCCAGGCCCTGC A G MTA1 Ensembl:ENSG00000182979 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:105469955..105470444 26863196 MeRIP-seq:(Medium) rs1452580419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40961,Human_RBP_ID_23614727,Human_RBP_ID_26921725 Human_Splice_Rec_1562144,Human_Splice_Rec_1562184,Human_Splice_Rec_1562222,Human_Splice_Rec_1562260,Human_Splice_Rec_1562300,Human_Splice_Rec_1562392,Human_Splice_Rec_1562432,Human_Splice_Rec_1562438,Human_Splice_Rec_1562442,Human_Splice_Rec_1562446,Human_Splice_Rec_1562448 65461 RMVar_ID_65461 Human_SNP_ID_568688196 m1A Human chr14 - 105470136 105470136 105470136 GTGGCCGCGGCGGCAGGGCCTGGCTCTGGCGCAGGGCGATGGGCTTGTAGGGCCGGCGGGCAGCA GTGGCCGCGGCGGCAGGGCCTGGCTCTGGCGCGGGGCGATGGGCTTGTAGGGCCGGCGGGCAGCA T C AL928654.2 Ensembl:ENSG00000257270 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105470014..105470213 26863196 MeRIP-seq:(Medium) rs1287360947 Functional Loss SNV dbSNP153 33..33 33 - - - 65462 RMVar_ID_65462 Human_SNP_ID_568688252 m1A Human chr14 + 105470227 105470226 105470227 CCCATCGTCATCGAGGACTAGGGGCCGCCCCCACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCA CCCATCGTCATCGAGGACTAGGGGCCGCCCCC_CCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCA CA C MTA1 Ensembl:ENSG00000182979 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:105470101..105470300 26863410 MeRIP-seq:(Medium) rs782744549 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_442453 Human_miRNA_ID_1702171 65463 RMVar_ID_65463 Human_SNP_ID_568688254 m1A Human chr14 + 105470227 105470227 105470227 CCCATCGTCATCGAGGACTAGGGGCCGCCCCCACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCA CCCATCGTCATCGAGGACTAGGGGCCGCCCCCCCCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCA A C MTA1 Ensembl:ENSG00000182979 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:105470101..105470300 26863410 MeRIP-seq:(Medium) rs1237398885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442453 Human_miRNA_ID_1702171 65464 RMVar_ID_65464 Human_SNP_ID_568688284 m1A Human chr14 + 105470259 105470256 105470259 ACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCACACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC ACCTGCGGCCGCCCCCCGCCCCTCGCCCGC___CACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC CCCA C MTA1 Ensembl:ENSG00000182979 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:105470223..105470310 26863410 MeRIP-seq:(Medium) rs1555434274 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17845697,Human_RBP_ID_25086575 65465 RMVar_ID_65465 Human_SNP_ID_568688289 m1A Human chr14 + 105470259 105470259 105470259 ACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCACACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC ACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCCCACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC A C MTA1 Ensembl:ENSG00000182979 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:105470223..105470310 26863410 MeRIP-seq:(Medium) rs587656396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17845697,Human_RBP_ID_25086575 65466 RMVar_ID_65466 Human_SNP_ID_568688290 m1A Human chr14 + 105470259 105470259 105470259 ACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCACACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC ACCTGCGGCCGCCCCCCGCCCCTCGCCCGCCCGCACGGCCCCTTCCCAGCCAGCCCGCCGCCCGC A G MTA1 Ensembl:ENSG00000182979 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:105470223..105470310 26863410 MeRIP-seq:(Medium) rs587656396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17845697,Human_RBP_ID_25086575 65467 RMVar_ID_65467 Human_SNP_ID_568689778 m1A Human chr14 + 105474881 105474881 105474881 CGGGCGCACCGACCATGGCCTCCAAATGCCCCAAGTGCGACAAGACCGTGTACTTCGGTGAGTGC CGGGCGCACCGACCATGGCCTCCAAATGCCCCTAGTGCGACAAGACCGTGTACTTCGGTGAGTGC A T CRIP2 Ensembl:ENSG00000182809 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105474774..105475716;chr14:105474801..105475439;chr14:105474776..105474976 26863196 MeRIP-seq:(Medium) rs782768323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1562465,Human_Splice_Rec_1562471,Human_Splice_Rec_1562483,Human_Splice_Rec_1562497,Human_Splice_Rec_1562505,Human_Splice_Rec_1562517 Human_miRNA_ID_2479349 RMVar_hsa_circ_79690,RMVar_hsa_circ_124848,RMVar_hsa_circ_169740,RMVar_hsa_circ_169741 65468 RMVar_ID_65468 Human_SNP_ID_568690187 m1A Human chr14 + 105476098 105476098 105476098 GGGCTTCCGGCTGCCTCTCCTGGAGCCCGCTCAGCCCTCAGTCTCTGTCCCAGCGAGGGCTGTCT GGGCTTCCGGCTGCCTCTCCTGGAGCCCGCTCCGCCCTCAGTCTCTGTCCCAGCGAGGGCTGTCT A C CRIP2 Ensembl:ENSG00000182809 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105476094..105476295 32194978 MeRIP-seq:(Medium) rs587742832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79690,RMVar_hsa_circ_124848,RMVar_hsa_circ_169740,RMVar_hsa_circ_169741 65469 RMVar_ID_65469 Human_SNP_ID_568690275 m1A Human chr14 - 105476397 105476397 105476397 CTGGGTTCTACTCAGGTATGAGCTGCGGGGGCAGCCTGGTGTGAGGGTGGGCAGGATTCTGGACC CTGGGTTCTACTCAGGTATGAGCTGCGGGGGCTGCCTGGTGTGAGGGTGGGCAGGATTCTGGACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105476396..105476544 26863196 MeRIP-seq:(Medium) rs1388888115 Functional Loss SNV dbSNP153 33..33 33 - - - 65470 RMVar_ID_65470 Human_SNP_ID_568690418 m1A Human chr14 - 105476816 105476816 105476816 TGGGCATGGCCAGGGCCAGCCTCCAGGACACCAGCCCAACCACAAGGCTGCACCAGCTTAGAGCC TGGGCATGGCCAGGGCCAGCCTCCAGGACACCGGCCCAACCACAAGGCTGCACCAGCTTAGAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105476813..105476914 32194978 MeRIP-seq:(Medium) rs1419754454 Functional Loss SNV dbSNP153 33..33 33 - - - 65471 RMVar_ID_65471 Human_SNP_ID_568690719 m1A Human chr14 - 105477700 105477695 105477700 ACCCGCTTCCCCCCACACACACCCGCTTCCTCAGACACACACCCGCTTCCCCCCACACACCTGCC ACCCGCTTCCCCCCACACACACCCGCTTCCTC_____CACACCCGCTTCCCCCCACACACCTGCC GTGTCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:105477561..105478500;chr14:105477362..105478525 26863196 MeRIP-seq:(Medium) rs1555436111 Functional Loss DEL dbSNP153 33..37 33 - - - 65472 RMVar_ID_65472 Human_SNP_ID_568690734 m1A Human chr14 - 105477700 105477700 105477700 ACCCGCTTCCCCCCACACACACCCGCTTCCTCAGACACACACCCGCTTCCCCCCACACACCTGCC ACCCGCTTCCCCCCACACACACCCGCTTCCTCCGACACACACCCGCTTCCCCCCACACACCTGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:105477561..105478500;chr14:105477362..105478525 26863196 MeRIP-seq:(Medium) rs868947009 Functional Loss SNV dbSNP153 33..33 33 - - - 65473 RMVar_ID_65473 Human_SNP_ID_568691121 m1A Human chr14 + 105478334 105478334 105478334 AGTTCTGCCTCAAGTGCGAGCGCTGCAGCAAGACGCTGACGCCCGGGGGCCACGCCGAGGTGAGC AGTTCTGCCTCAAGTGCGAGCGCTGCAGCAAGTCGCTGACGCCCGGGGGCCACGCCGAGGTGAGC A T CRIP2 Ensembl:ENSG00000182809 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr14:105478239..105478525;chr14:105477262..105478376 26863196,32194978 MeRIP-seq:(Medium) rs1555436350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1562452,Human_Splice_Rec_1562453,Human_Splice_Rec_1562484,Human_Splice_Rec_1562485,Human_Splice_Rec_1562498,Human_Splice_Rec_1562506,Human_Splice_Rec_1562507,Human_Splice_Rec_1562518,Human_Splice_Rec_1562519,Human_Splice_Rec_1562532,Human_Splice_Rec_1562533,Human_Splice_Rec_1562538,Human_Splice_Rec_1562539,Human_Splice_Rec_1562552,Human_Splice_Rec_1562553 Human_miRNA_ID_1264660,Human_miRNA_ID_2611498 RMVar_hsa_circ_81832,RMVar_hsa_circ_79690,RMVar_hsa_circ_124848,RMVar_hsa_circ_169740,RMVar_hsa_circ_85366,RMVar_hsa_circ_169741,RMVar_hsa_circ_169743,RMVar_hsa_circ_53780,RMVar_hsa_circ_169742 65474 RMVar_ID_65474 Human_SNP_ID_568691804 m1A Human chr14 + 105479434 105479434 105479434 GGACTCCTCCCTCAGCACCCACCTTCTGCCCCAGCACGACGGCCAGCCCTACTGCCACAAGCCCT GGACTCCTCCCTCAGCACCCACCTTCTGCCCCCGCACGACGGCCAGCCCTACTGCCACAAGCCCT A C CRIP2 Ensembl:ENSG00000182809 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:105479426..105479500 26863196 MeRIP-seq:(Medium) rs1555436843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883256,Human_RBP_ID_19064525 Human_Splice_Rec_1562463,Human_Splice_Rec_1562469,Human_Splice_Rec_1562481,Human_Splice_Rec_1562495,Human_Splice_Rec_1562515,Human_Splice_Rec_1562527,Human_Splice_Rec_1562549,Human_Splice_Rec_1562563 RMVar_hsa_circ_81832,RMVar_hsa_circ_79690,RMVar_hsa_circ_124848,RMVar_hsa_circ_169740,RMVar_hsa_circ_85366,RMVar_hsa_circ_169741,RMVar_hsa_circ_88154,RMVar_hsa_circ_169743,RMVar_hsa_circ_169742,RMVar_hsa_circ_113885,RMVar_hsa_circ_169745,RMVar_hsa_circ_109191,RMVar_hsa_circ_169746,RMVar_hsa_circ_169747 65475 RMVar_ID_65475 Human_SNP_ID_568692040 m1A Human chr14 - 105479825 105479825 105479825 GCCCAGAGGATGCCAGAGGGGGCAGACACACCAGAGACTCGGGGATGGGCATGGTGCTCTGCCCG GCCCAGAGGATGCCAGAGGGGGCAGACACACCGGAGACTCGGGGATGGGCATGGTGCTCTGCCCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:105479776..105479925 32194978 MeRIP-seq:(Medium) rs1042632665 Functional Loss SNV dbSNP153 33..33 33 - - - 65476 RMVar_ID_65476 Human_SNP_ID_568694439 m1A Human chr14 + 105487253 105487253 105487253 GCCCCAGCCGCTGCCGCCTGCACCGGACCCGGAGCCGTCATGCCCAAGTGTCCCAAGTGCAACAA GCCCCAGCCGCTGCCGCCTGCACCGGACCCGGGGCCGTCATGCCCAAGTGTCCCAAGTGCAACAA A G AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:105487201..105487300 26863196 MeRIP-seq:(Medium) rs782426697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757547,Human_RBP_ID_4308158 Human_Splice_Rec_1562571,Human_Splice_Rec_1562580,Human_Splice_Rec_1562581,Human_Splice_Rec_1562590,Human_Splice_Rec_1562591,Human_Splice_Rec_1562607 Human_miRNA_ID_2479350 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_169749 65477 RMVar_ID_65477 Human_SNP_ID_568694444 m1A Human chr14 - 105487258 105487258 105487258 CCTCCTTGTTGCACTTGGGACACTTGGGCATGACGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT CCTCCTTGTTGCACTTGGGACACTTGGGCATGTCGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105487161..105487438;chr14:105487201..105487372;chr14:105487201..105487360 26863196 MeRIP-seq:(Medium) rs7140395 Functional Loss SNV dbSNP153 33..33 33 - - - 65478 RMVar_ID_65478 Human_SNP_ID_568694445 m1A Human chr14 - 105487258 105487258 105487258 CCTCCTTGTTGCACTTGGGACACTTGGGCATGACGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT CCTCCTTGTTGCACTTGGGACACTTGGGCATGGCGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105487161..105487438;chr14:105487201..105487372;chr14:105487201..105487360 26863196 MeRIP-seq:(Medium) rs7140395 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 65479 RMVar_ID_65479 Human_SNP_ID_568694446 m1A Human chr14 - 105487258 105487258 105487258 CCTCCTTGTTGCACTTGGGACACTTGGGCATGACGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT CCTCCTTGTTGCACTTGGGACACTTGGGCATGCCGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105487161..105487438;chr14:105487201..105487372;chr14:105487201..105487360 26863196 MeRIP-seq:(Medium) rs7140395 Functional Loss SNV dbSNP153 33..33 33 - - - 65480 RMVar_ID_65480 Human_SNP_ID_568694477 m1A Human chr14 - 105487297 105487297 105487297 TCCTCGCGGGGCCGGTGTGGGCGCGCTCACCGAAGTACACCTCCTTGTTGCACTTGGGACACTTG TCCTCGCGGGGCCGGTGTGGGCGCGCTCACCGCAGTACACCTCCTTGTTGCACTTGGGACACTTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:105487258..105487388 26863196 MeRIP-seq:(Medium) rs1308419509 Functional Loss SNV dbSNP153 33..33 33 - - - 65481 RMVar_ID_65481 Human_SNP_ID_568694812 m1A Human chr14 - 105488200 105488200 105488200 TTCCCACATTTCTCGCACTTCAGGCAGGGCCGATGCCAGTCCTTGCCCAGAGAGGTCACCCTCTC TTCCCACATTTCTCGCACTTCAGGCAGGGCCGCTGCCAGTCCTTGCCCAGAGAGGTCACCCTCTC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:105488101..105488200 26863196 MeRIP-seq:(Medium) rs782799325 Functional Loss SNV dbSNP153 33..33 33 - - - 65482 RMVar_ID_65482 Human_SNP_ID_568694818 m1A Human chr14 + 105488213 105488213 105488213 CTCTGGGCAAGGACTGGCATCGGCCCTGCCTGAAGTGCGAGAAATGTGGGAAGACGCTGACCTCT CTCTGGGCAAGGACTGGCATCGGCCCTGCCTGGAGTGCGAGAAATGTGGGAAGACGCTGACCTCT A G AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding CDS,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:105488176..105488225 26863196 MeRIP-seq:(Medium) rs373845386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4309143,Human_RBP_ID_5112505,Human_RBP_ID_22438988 Human_Splice_Rec_1562572,Human_Splice_Rec_1562573,Human_Splice_Rec_1562582,Human_Splice_Rec_1562583,Human_Splice_Rec_1562592,Human_Splice_Rec_1562593,Human_Splice_Rec_1562601,Human_Splice_Rec_1562608,Human_Splice_Rec_1562609,Human_Splice_Rec_1562625,Human_Splice_Rec_1562633,Human_Splice_Rec_1562643,Human_Splice_Rec_1562653 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750 65483 RMVar_ID_65483 Human_SNP_ID_568694826 m1A Human chr14 + 105488231 105488231 105488231 ATCGGCCCTGCCTGAAGTGCGAGAAATGTGGGAAGACGCTGACCTCTGGGGGCCACGCTGAGGTA ATCGGCCCTGCCTGAAGTGCGAGAAATGTGGGCAGACGCTGACCTCTGGGGGCCACGCTGAGGTA A C AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105487201..105488341 26863196 MeRIP-seq:(Medium) rs782403146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112505,Human_RBP_ID_17651502,Human_RBP_ID_19064526,Human_RBP_ID_22439500 Human_Splice_Rec_1562572,Human_Splice_Rec_1562573,Human_Splice_Rec_1562582,Human_Splice_Rec_1562583,Human_Splice_Rec_1562592,Human_Splice_Rec_1562593,Human_Splice_Rec_1562601,Human_Splice_Rec_1562608,Human_Splice_Rec_1562609,Human_Splice_Rec_1562625,Human_Splice_Rec_1562633,Human_Splice_Rec_1562643,Human_Splice_Rec_1562653 Human_miRNA_ID_2469366 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750 65484 RMVar_ID_65484 Human_SNP_ID_568694827 m1A Human chr14 + 105488231 105488231 105488231 ATCGGCCCTGCCTGAAGTGCGAGAAATGTGGGAAGACGCTGACCTCTGGGGGCCACGCTGAGGTA ATCGGCCCTGCCTGAAGTGCGAGAAATGTGGGGAGACGCTGACCTCTGGGGGCCACGCTGAGGTA A G AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:105487201..105488341 26863196 MeRIP-seq:(Medium) rs782403146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112505,Human_RBP_ID_17651502,Human_RBP_ID_19064526,Human_RBP_ID_22439500 Human_Splice_Rec_1562572,Human_Splice_Rec_1562573,Human_Splice_Rec_1562582,Human_Splice_Rec_1562583,Human_Splice_Rec_1562592,Human_Splice_Rec_1562593,Human_Splice_Rec_1562601,Human_Splice_Rec_1562608,Human_Splice_Rec_1562609,Human_Splice_Rec_1562625,Human_Splice_Rec_1562633,Human_Splice_Rec_1562643,Human_Splice_Rec_1562653 Human_miRNA_ID_2469366 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750 65485 RMVar_ID_65485 Human_SNP_ID_568694828 m1A Human chr14 + 105488232 105488232 105488232 TCGGCCCTGCCTGAAGTGCGAGAAATGTGGGAAGACGCTGACCTCTGGGGGCCACGCTGAGGTAG TCGGCCCTGCCTGAAGTGCGAGAAATGTGGGATGACGCTGACCTCTGGGGGCCACGCTGAGGTAG A T AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding CDS,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:105488076..105488276 26863196 MeRIP-seq:(Medium) rs782176146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112505,Human_RBP_ID_17651502,Human_RBP_ID_19064526 Human_Splice_Rec_1562572,Human_Splice_Rec_1562573,Human_Splice_Rec_1562582,Human_Splice_Rec_1562583,Human_Splice_Rec_1562592,Human_Splice_Rec_1562593,Human_Splice_Rec_1562601,Human_Splice_Rec_1562608,Human_Splice_Rec_1562609,Human_Splice_Rec_1562625,Human_Splice_Rec_1562633,Human_Splice_Rec_1562643,Human_Splice_Rec_1562653 Human_miRNA_ID_2469366 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750 65486 RMVar_ID_65486 Human_SNP_ID_568694833 m1A Human chr14 - 105488238 105488238 105488238 TCCCACCTACCTCAGCGTGGCCCCCAGAGGTCAGCGTCTTCCCACATTTCTCGCACTTCAGGCAG TCCCACCTACCTCAGCGTGGCCCCCAGAGGTCGGCGTCTTCCCACATTTCTCGCACTTCAGGCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105487880..105488327 26863196 MeRIP-seq:(Medium) rs368067080 Functional Loss SNV dbSNP153 33..33 33 - - - 65487 RMVar_ID_65487 Human_SNP_ID_568694883 m1A Human chr14 + 105488340 105488340 105488340 CCTCACGGCCCTTCTCTTTGCAGCACGAAGGCAAACCCTACTGCAACCACCCCTGCTACGCAGCC CCTCACGGCCCTTCTCTTTGCAGCACGAAGGCCAACCCTACTGCAACCACCCCTGCTACGCAGCC A C AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105487806..105488475 26863196 MeRIP-seq:(Medium) rs1555438501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883250,Human_RBP_ID_22438990 Human_Splice_Rec_1562567,Human_Splice_Rec_1562574,Human_Splice_Rec_1562575,Human_Splice_Rec_1562584,Human_Splice_Rec_1562585,Human_Splice_Rec_1562594,Human_Splice_Rec_1562595,Human_Splice_Rec_1562602,Human_Splice_Rec_1562603,Human_Splice_Rec_1562610,Human_Splice_Rec_1562611,Human_Splice_Rec_1562619,Human_Splice_Rec_1562626,Human_Splice_Rec_1562627,Human_Splice_Rec_1562634,Human_Splice_Rec_1562635,Human_Splice_Rec_1562644,Human_Splice_Rec_1562645,Human_Splice_Rec_1562654,Human_Splice_Rec_1562655 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_26380,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750 65488 RMVar_ID_65488 Human_SNP_ID_568695094 m1A Human chr14 + 105488717 105488717 105488717 CTGCTTGCAGGGCCACTGTCCAGGCAAATGCCAGGCCTTGTCCCCAGATGCCCAGGGCTCCCTTG CTGCTTGCAGGGCCACTGTCCAGGCAAATGCCCGGCCTTGTCCCCAGATGCCCAGGGCTCCCTTG A C AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105488624..105488723 26863196 MeRIP-seq:(Medium) rs1283414328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112791,Human_RBP_ID_8400975,Human_RBP_ID_17651512 Human_Splice_Rec_1562570,Human_Splice_Rec_1562578,Human_Splice_Rec_1562588,Human_Splice_Rec_1562598,Human_Splice_Rec_1562600,Human_Splice_Rec_1562606,Human_Splice_Rec_1562638,Human_Splice_Rec_1562639,Human_Splice_Rec_1562648,Human_Splice_Rec_1562658 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750,RMVar_hsa_circ_113012,RMVar_hsa_circ_91783,RMVar_hsa_circ_169751,RMVar_hsa_circ_169752 65489 RMVar_ID_65489 Human_SNP_ID_568695095 m1A Human chr14 + 105488717 105488717 105488717 CTGCTTGCAGGGCCACTGTCCAGGCAAATGCCAGGCCTTGTCCCCAGATGCCCAGGGCTCCCTTG CTGCTTGCAGGGCCACTGTCCAGGCAAATGCCGGGCCTTGTCCCCAGATGCCCAGGGCTCCCTTG A G AL928654.3,CRIP1 Ensembl:ENSG00000257341,Ensembl:ENSG00000213145 Protein coding,Protein coding intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105488624..105488723 26863196 MeRIP-seq:(Medium) rs1283414328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112791,Human_RBP_ID_8400975,Human_RBP_ID_17651512 Human_Splice_Rec_1562570,Human_Splice_Rec_1562578,Human_Splice_Rec_1562588,Human_Splice_Rec_1562598,Human_Splice_Rec_1562600,Human_Splice_Rec_1562606,Human_Splice_Rec_1562638,Human_Splice_Rec_1562639,Human_Splice_Rec_1562648,Human_Splice_Rec_1562658 RMVar_hsa_circ_118239,RMVar_hsa_circ_120326,RMVar_hsa_circ_169748,RMVar_hsa_circ_116426,RMVar_hsa_circ_169749,RMVar_hsa_circ_169750,RMVar_hsa_circ_113012,RMVar_hsa_circ_91783,RMVar_hsa_circ_169751,RMVar_hsa_circ_169752 65490 RMVar_ID_65490 Human_SNP_ID_568695589 m1A Human chr14 - 105490239 105490179 105490239 ACGAGAGGCGCAGCCCGAGGGGTCCCGGCCCCACCTTTCTTCTCGGCCTCCTTCGCCCCCGACCT ACGAGAGGCGCAGCCCGAGGGGTCCCGGCCCC_________________________________ CGGGGCCGGGAGGGCCGCCTGGAAGAGGAGGTCGGGGGCGAAGGAGGCCGAGAAGAAAGGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105490234..105490393 26863196 MeRIP-seq:(Medium) rs1567070990 Functional Loss DEL dbSNP153 33..65 33 - - - 65491 RMVar_ID_65491 Human_SNP_ID_568695618 m1A Human chr14 + 105490234 105490230 105490234 AGAGGAGGTCGGGGGCGAAGGAGGCCGAGAAGAAAGGTGGGGCCGGGACCCCTCGGGCTGCGCCT AGAGGAGGTCGGGGGCGAAGGAGGCCGAG____AAGGTGGGGCCGGGACCCCTCGGGCTGCGCCT GAAGA G AL928654.3,TEDC1 Ensembl:ENSG00000257341,Ensembl:ENSG00000185347 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105490197..105490393 26863196 MeRIP-seq:(Medium) rs1252171776 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_1562697,Human_Splice_Rec_1562713,Human_Splice_Rec_1562727 65492 RMVar_ID_65492 Human_SNP_ID_568696022 m1A Human chr14 + 105491356 105491356 105491356 GCCCCGGGCCGCGGCGGAGGCGGGCGATCCGAAAGAGGCTGGTGCTGGCTGCATGGGGAGGCGGC GCCCCGGGCCGCGGCGGAGGCGGGCGATCCGAGAGAGGCTGGTGCTGGCTGCATGGGGAGGCGGC A G AL928654.3,TEDC1 Ensembl:ENSG00000257341,Ensembl:ENSG00000185347 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105490792..105492121 26863196 MeRIP-seq:(Medium) rs1355597148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4285813 65493 RMVar_ID_65493 Human_SNP_ID_568696037 m1A Human chr14 + 105491401 105491401 105491401 TGGCTGCATGGGGAGGCGGCGGCAGCGGGTGGACCCCGCGGCTGGGGCCCGGGCCGGGGCCCTGC TGGCTGCATGGGGAGGCGGCGGCAGCGGGTGGTCCCCGCGGCTGGGGCCCGGGCCGGGGCCCTGC A T AL928654.3,TEDC1 Ensembl:ENSG00000257341,Ensembl:ENSG00000185347 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:105491353..105491482 26863196 MeRIP-seq:(Medium) rs1299035556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4285816 65494 RMVar_ID_65494 Human_SNP_ID_568698445 m1A Human chr14 - 105497419 105497419 105497419 TTCCTCACCATCCACCGCCAGAAGACCAGCTCAGAGCGCCGCCACGCCAGGACAGCCTCCAGGCG TTCCTCACCATCCACCGCCAGAAGACCAGCTCGGAGCGCCGCCACGCCAGGACAGCCTCCAGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105497286..105497493 26863196 MeRIP-seq:(Medium) rs1311549935 Functional Loss SNV dbSNP153 33..33 33 - - - 65495 RMVar_ID_65495 Human_SNP_ID_568698914 m1A Human chr14 + 105498647 105498647 105498647 AGGCTGGAGGCTGTGGACGGGGGCCAGAGTGGAGTGCCGCGCGGCGGGCCTCTCGGGAGGCTGTG AGGCTGGAGGCTGTGGACGGGGGCCAGAGTGGGGTGCCGCGCGGCGGGCCTCTCGGGAGGCTGTG A G TEDC1 Ensembl:ENSG00000185347 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105497736..105498875;chr14:105497776..105499205;chr14:105497776..105499185;chr14:105497786..105498876 26863196 MeRIP-seq:(Medium) rs1555441002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442474,Human_RBP_ID_881181,Human_RBP_ID_9353027 Human_Splice_Rec_1562678,Human_Splice_Rec_1562712,Human_Splice_Rec_1562726,Human_Splice_Rec_1562740,Human_Splice_Rec_1562778,Human_Splice_Rec_1562794,Human_Splice_Rec_1562810,Human_Splice_Rec_1562838,Human_Splice_Rec_1562848,Human_Splice_Rec_1562860,Human_Splice_Rec_1562862,Human_Splice_Rec_1562864 RMVar_hsa_circ_169755,RMVar_hsa_circ_91170 65496 RMVar_ID_65496 Human_SNP_ID_568706797 m1A Human chr14 - 105526791 105526791 105526791 CAGGGCCGGGTCCCCGTCACCCCGCCGGCCCCAGGCCTCACCCCTGCCGCATCGGCCCCCGCCCC CAGGGCCGGGTCCCCGTCACCCCGCCGGCCCCCGGCCTCACCCCTGCCGCATCGGCCCCCGCCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr14:105526675..105526912;chr14:105526671..105526820 26863196 MeRIP-seq:(Medium) rs1314290835 Functional Loss SNV dbSNP153 33..33 33 - - - 65497 RMVar_ID_65497 Human_SNP_ID_568707603 m1A Human chr14 - 105529420 105529420 105529420 GCCCTGCATGCTGACCTCGCTGAGCGCCACGCACGGCAGCACCAGCAGCAGCATGTAGCAGTAGA GCCCTGCATGCTGACCTCGCTGAGCGCCACGCGCGGCAGCACCAGCAGCAGCATGTAGCAGTAGA T C lnc-BRF1-42,lnc-BRF1-42:2,lnc-BRF1-42:3,lnc-BRF1-42:4,lnc-BRF1-42:5,lnc-BRF1-42:6 RNACentral:URS00008C1EE0,RNACentral:URS00009B5B96,RNACentral:URS00009BB96C,RNACentral:URS00008BB075,RNACentral:URS00008B6654,RNACentral:URS00008B6EE0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105528786..105529421 32194978 MeRIP-seq:(Medium) rs1368786816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119592,RMVar_hsa_circ_169756 65498 RMVar_ID_65498 Human_SNP_ID_568743703 m1A Human chr14 - 105627815 105627815 105627815 TCAGGCGACCGGGGCAGAGCAGCCTCAGGTGAAAAGGGCCGGTGGGGGGCAGGAGGAGCAAGGGG TCAGGCGACCGGGGCAGAGCAGCCTCAGGTGAGAAGGGCCGGTGGGGGGCAGGAGGAGCAAGGGG T C lnc-BRF1-42,lnc-BRF1-42:2,lnc-BRF1-42:3,lnc-BRF1-42:4,lnc-BRF1-42:5,COPDA1,lnc-BRF1-42:6 RNACentral:URS00008C1EE0,RNACentral:URS00009B5B96,RNACentral:URS00009BB96C,RNACentral:URS00008BB075,RNACentral:URS00008B6654,RNACentral:URS00009B1E41,RNACentral:URS00008B6EE0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105627765..105628044 26863196 MeRIP-seq:(Medium) rs1271921360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128162,RMVar_hsa_circ_169758,RMVar_hsa_circ_123366,RMVar_hsa_circ_169757 65499 RMVar_ID_65499 Human_SNP_ID_568744025 m1A Human chr14 - 105628343 105628343 105628343 CACAGGTGAGCAGGGCAGGTGGGGGTAGAAGGAGCAGGGGGCAGCTCCTGGAACTCAGGGGACCA CACAGGTGAGCAGGGCAGGTGGGGGTAGAAGGTGCAGGGGGCAGCTCCTGGAACTCAGGGGACCA T A lnc-BRF1-42,lnc-BRF1-42:2,lnc-BRF1-42:3,lnc-BRF1-42:4,lnc-BRF1-42:5,COPDA1,lnc-BRF1-42:6 RNACentral:URS00008C1EE0,RNACentral:URS00009B5B96,RNACentral:URS00009BB96C,RNACentral:URS00008BB075,RNACentral:URS00008B6654,RNACentral:URS00009B1E41,RNACentral:URS00008B6EE0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:105628293..105628457 26863196 MeRIP-seq:(Medium) rs1210743533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128162,RMVar_hsa_circ_169758,RMVar_hsa_circ_123366,RMVar_hsa_circ_169757 65500 RMVar_ID_65500 Human_SNP_ID_240778682 m1A Human chr5 + 90407823 90407823 90407823 CTCTTCTTTTTTTCCTCTTTGTTTTGTCCACTACAAGCTCACTTCTATGAAATGGAAAGAAAAAG CTCTTCTTTTTTTCCTCTTTGTTTTGTCCACTGCAAGCTCACTTCTATGAAATGGAAAGAAAAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:90407774..90407892 26863196 MeRIP-seq:(Medium) rs1191891828 Functional Loss SNV dbSNP153 33..33 33 - - - 65501 RMVar_ID_65501 Human_SNP_ID_240779198 m1A Human chr5 + 90409660 90409660 90409660 GCCTCCTTATTACCGACCTCAGAGCTAAACTCATTATCTCTTCGCACAGAGACGTTCCTCTCAAG GCCTCCTTATTACCGACCTCAGAGCTAAACTCGTTATCTCTTCGCACAGAGACGTTCCTCTCAAG A G lnc-POLR3G-9 RNACentral:URS0000D5E1FB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:90407729..90409738 26863196 MeRIP-seq:(Medium) rs781566717 Functional Loss SNV dbSNP153 33..33 33 - - - 65502 RMVar_ID_65502 Human_SNP_ID_240779199 m1A Human chr5 + 90409660 90409660 90409660 GCCTCCTTATTACCGACCTCAGAGCTAAACTCATTATCTCTTCGCACAGAGACGTTCCTCTCAAG GCCTCCTTATTACCGACCTCAGAGCTAAACTCTTTATCTCTTCGCACAGAGACGTTCCTCTCAAG A T lnc-POLR3G-9 RNACentral:URS0000D5E1FB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:90407729..90409738 26863196 MeRIP-seq:(Medium) rs781566717 Functional Loss SNV dbSNP153 33..33 33 - - - 65503 RMVar_ID_65503 Human_SNP_ID_240779215 m1A Human chr5 + 90409697 90409697 90409697 CTCTTCGCACAGAGACGTTCCTCTCAAGAACGATTTTAACCCCCTACCCAAGGCAGCAAGACGCC CTCTTCGCACAGAGACGTTCCTCTCAAGAACGGTTTTAACCCCCTACCCAAGGCAGCAAGACGCC A G lnc-POLR3G-9 RNACentral:URS0000D5E1FB lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:90409544..90409734 26863196 MeRIP-seq:(Medium) rs760414310 Functional Loss SNV dbSNP153 33..33 33 - - - 65504 RMVar_ID_65504 Human_SNP_ID_240779216 m1A Human chr5 - 90409698 90409698 90409698 GGGCGTCTTGCTGCCTTGGGTAGGGGGTTAAAATCGTTCTTGAGAGGAACGTCTCTGTGCGAAGA GGGCGTCTTGCTGCCTTGGGTAGGGGGTTAAAGTCGTTCTTGAGAGGAACGTCTCTGTGCGAAGA T C CETN3 Ensembl:ENSG00000153140 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:90409596..90409750 26863196 MeRIP-seq:(Medium) rs766130292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845836,Human_RBP_ID_8943888,Human_RBP_ID_24121224,Human_RBP_ID_27826554 Human_Splice_Rec_671541,Human_Splice_Rec_671549,Human_Splice_Rec_671559,Human_Splice_Rec_671575,Human_Splice_Rec_671581 RMVar_hsa_circ_3679 65505 RMVar_ID_65505 Human_SNP_ID_240797625 m1A Human chr5 + 90488043 90488043 90488043 TAAACCAGTGCCACTGAAAACAGGAGAAGGTGAAGAATATATGCTGGCTTTGAAACAGGAGTTGA TAAACCAGTGCCACTGAAAACAGGAGAAGGTGGAGAATATATGCTGGCTTTGAAACAGGAGTTGA A G POLR3G Ensembl:ENSG00000113356 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:90488037..90490600 32194978 MeRIP-seq:(Medium) rs763336214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_671594,Human_Splice_Rec_671595,Human_Splice_Rec_671600,Human_Splice_Rec_671601,Human_Splice_Rec_671614,Human_Splice_Rec_671615,Human_Splice_Rec_671622,Human_Splice_Rec_671623,Human_Splice_Rec_671636,Human_Splice_Rec_671637,Human_Splice_Rec_671650,Human_Splice_Rec_671651,Human_Splice_Rec_671664,Human_Splice_Rec_671665 Human_miRNA_ID_2440829 RMVar_hsa_circ_57374,RMVar_hsa_circ_233098,RMVar_hsa_circ_116384,RMVar_hsa_circ_343167,RMVar_hsa_circ_60487,RMVar_hsa_circ_345275,RMVar_hsa_circ_233100,RMVar_hsa_circ_318425,RMVar_hsa_circ_331273 65506 RMVar_ID_65506 Human_SNP_ID_240801922 m1A Human chr5 + 90506591 90506591 90506591 CAGATGAGGAAAATGAAGAGAAAGAAGGAAGCAAAGAGAAAAGTAAAGAAGGTGATGATGACGAT CAGATGAGGAAAATGAAGAGAAAGAAGGAAGCGAAGAGAAAAGTAAAGAAGGTGATGATGACGAT A G POLR3G Ensembl:ENSG00000113356 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:90495715..90506645 32194978 MeRIP-seq:(Medium) rs780643907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26351029,Human_RBP_ID_27826555 Human_Splice_Rec_671608,Human_Splice_Rec_671609,Human_Splice_Rec_671630,Human_Splice_Rec_671631,Human_Splice_Rec_671644,Human_Splice_Rec_671645,Human_Splice_Rec_671658,Human_Splice_Rec_671659 RMVar_hsa_circ_57374,RMVar_hsa_circ_343167,RMVar_hsa_circ_233101,RMVar_hsa_circ_301719 65507 RMVar_ID_65507 Human_SNP_ID_240801924 m1A Human chr5 - 90506602 90506602 90506602 GCATCATCGTCATCGTCATCATCACCTTCTTTACTTTTCTCTTTGCTTCCTTCTTTCTCTTCATT GCATCATCGTCATCGTCATCATCACCTTCTTTGCTTTTCTCTTTGCTTCCTTCTTTCTCTTCATT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:90506551..90506675 26863196 MeRIP-seq:(Medium) rs1183559483 Functional Loss SNV dbSNP153 33..33 33 - - - 65508 RMVar_ID_65508 Human_SNP_ID_240806332 m1A Human chr5 - 90525270 90525270 90525270 AGATTTTAACATTATGGCAGGGAGGCATCAGAATCGTAGTTTTCCTCTTCCAGGAGTTCAGTCAA AGATTTTAACATTATGGCAGGGAGGCATCAGAGTCGTAGTTTTCCTCTTCCAGGAGTTCAGTCAA T C LYSMD3 Ensembl:ENSG00000176018 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:90525228..90525334 26863196 MeRIP-seq:(Medium) rs368685200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_648410,Human_RBP_ID_18055502 Human_Splice_Rec_671670,Human_Splice_Rec_671674,Human_Splice_Rec_671678,Human_Splice_Rec_671682 RMVar_hsa_circ_73902,RMVar_hsa_circ_233102,RMVar_hsa_circ_78834,RMVar_hsa_circ_233103,RMVar_hsa_circ_62019 65509 RMVar_ID_65509 Human_SNP_ID_240807298 m1A Human chr5 - 90529525 90529525 90529525 GGACGGGGTCAGCCCAAAGCAGAGGCTCGGCCATGAACTTACCCGGGACAGCGGCGGCGGCGGAC GGACGGGGTCAGCCCAAAGCAGAGGCTCGGCCGTGAACTTACCCGGGACAGCGGCGGCGGCGGAC T C LYSMD3 Ensembl:ENSG00000176018 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:90529339..90529570 26863196 MeRIP-seq:(Medium) rs1388608037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4843066,Human_RBP_ID_15543995,Human_RBP_ID_27825580 Human_Splice_Rec_671667,Human_Splice_Rec_671673,Human_Splice_Rec_671677,Human_Splice_Rec_671681 65510 RMVar_ID_65510 Human_SNP_ID_240807317 m1A Human chr5 - 90529547 90529547 90529547 CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCAGCCCAAAGCAGAGGCTCGGCCATGAACTTACC CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCTGCCCAAAGCAGAGGCTCGGCCATGAACTTACC T A LYSMD3 Ensembl:ENSG00000176018 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:90529417..90529568 26863196 MeRIP-seq:(Medium) rs1483726659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15543996,Human_RBP_ID_27825580 Human_Splice_Rec_671667,Human_Splice_Rec_671673,Human_Splice_Rec_671677,Human_Splice_Rec_671681 65511 RMVar_ID_65511 Human_SNP_ID_240807318 m1A Human chr5 - 90529547 90529547 90529547 CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCAGCCCAAAGCAGAGGCTCGGCCATGAACTTACC CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCGGCCCAAAGCAGAGGCTCGGCCATGAACTTACC T C LYSMD3 Ensembl:ENSG00000176018 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:90529417..90529568 26863196 MeRIP-seq:(Medium) rs1483726659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15543996,Human_RBP_ID_27825580 Human_Splice_Rec_671667,Human_Splice_Rec_671673,Human_Splice_Rec_671677,Human_Splice_Rec_671681 65512 RMVar_ID_65512 Human_SNP_ID_240807319 m1A Human chr5 - 90529547 90529547 90529547 CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCAGCCCAAAGCAGAGGCTCGGCCATGAACTTACC CGTTGGCGGCAGAGGCGGAGGCGGACGGGGTCCGCCCAAAGCAGAGGCTCGGCCATGAACTTACC T G LYSMD3 Ensembl:ENSG00000176018 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:90529417..90529568 26863196 MeRIP-seq:(Medium) rs1483726659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15543996,Human_RBP_ID_27825580 Human_Splice_Rec_671667,Human_Splice_Rec_671673,Human_Splice_Rec_671677,Human_Splice_Rec_671681 65513 RMVar_ID_65513 Human_SNP_ID_240993533 m1A Human chr5 - 91310967 91310967 91310967 AGGAGGGCGGAAGGAAAGGAAGAAGGGAGAGAAGAAGAGAAGAAAGAAGCAGAGAAAGGAAGAGA AGGAGGGCGGAAGGAAAGGAAGAAGGGAGAGAGGAAGAGAAGAAAGAAGCAGAGAAAGGAAGAGA T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:91310916..91311035 26863196 MeRIP-seq:(Medium) rs963298678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838906,Human_RBP_ID_944393,Human_RBP_ID_24548113 Human_Splice_Rec_672724,Human_Splice_Rec_672746,Human_Splice_Rec_672790,Human_Splice_Rec_672886,Human_Splice_Rec_672898,Human_Splice_Rec_672916,Human_Splice_Rec_672924,Human_Splice_Rec_672936,Human_Splice_Rec_672944,Human_Splice_Rec_672952,Human_Splice_Rec_672958,Human_Splice_Rec_672966,Human_Splice_Rec_672974,Human_Splice_Rec_672984,Human_Splice_Rec_672990 65514 RMVar_ID_65514 Human_SNP_ID_241004560 m1A Human chr5 + 91354711 91354711 91354711 GATCACCATGATGCAGAATCCACACCAGTACAAGATCCCAGGCTGGTTCTTGAACAGACAGAAGG GATCACCATGATGCAGAATCCACACCAGTACAGGATCCCAGGCTGGTTCTTGAACAGACAGAAGG A G AC008799.1 Ensembl:ENSG00000240388 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:91354566..91354710 26863196 MeRIP-seq:(Medium) rs905979613 Functional Loss SNV dbSNP153 33..33 33 - - - 65515 RMVar_ID_65515 Human_SNP_ID_241537460 m1A Human chr5 - 93580599 93580599 93580599 AGGAGAACGCGGAGAGAGACGAAGGGAGTGGGAGACCAGCGACAGCGAGCGCCAGGGCACCGCAG AGGAGAACGCGGAGAGAGACGAAGGGAGTGGGGGACCAGCGACAGCGAGCGCCAGGGCACCGCAG T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:93580550..93580701 26863196 MeRIP-seq:(Medium) rs977386702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5614822 Human_Splice_Rec_673590 65516 RMVar_ID_65516 Human_SNP_ID_241537617 m1A Human chr5 - 93581147 93581147 93581147 TAAAGGTGGAAGTAAATGGCCACGCTGTATTGACAGAGGTAGGGTTTGTTTTTTAATACTCGTTC TAAAGGTGGAAGTAAATGGCCACGCTGTATTGTCAGAGGTAGGGTTTGTTTTTTAATACTCGTTC T A NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:93581145..93581265 26863196 MeRIP-seq:(Medium) rs1375223789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612735 Human_Splice_Rec_673217,Human_Splice_Rec_673283,Human_Splice_Rec_673291,Human_Splice_Rec_673299,Human_Splice_Rec_673343,Human_Splice_Rec_673357,Human_Splice_Rec_673375,Human_Splice_Rec_673399,Human_Splice_Rec_673411,Human_Splice_Rec_673429,Human_Splice_Rec_673445,Human_Splice_Rec_673457,Human_Splice_Rec_673471,Human_Splice_Rec_673495,Human_Splice_Rec_673521,Human_Splice_Rec_673531,Human_Splice_Rec_673553,Human_Splice_Rec_673567,Human_Splice_Rec_673589,Human_Splice_Rec_673795,Human_Splice_Rec_673807,Human_Splice_Rec_673827,Human_Splice_Rec_673839 65517 RMVar_ID_65517 Human_SNP_ID_241538175 m1A Human chr5 - 93581937 93581934 93581938 GAGAGAGACCCAGAGAGAGAGGAGAGAGAGAGAGACCCAGAGAGAGAGAGAGAGAGAGAGACCCA GAGAGAGACCCAGAGAGAGAGGAGAGAGAGA____CCCAGAGAGAGAGAGAGAGAGAGAGACCCA GTCTC G NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:93581886..93582029 26863196 MeRIP-seq:(Medium) rs1165830435 Functional Loss DEL dbSNP153 32..35 33 - - - 65518 RMVar_ID_65518 Human_SNP_ID_241538176 m1A Human chr5 - 93581937 93581934 93581938 GAGAGAGACCCAGAGAGAGAGGAGAGAGAGAGAGACCCAGAGAGAGAGAGAGAGAGAGAGACCCA GAGAGAGACCCAGAGAGAGAGGAGAGAGAGA__GACCCAGAGAGAGAGAGAGAGAGAGAGACCCA GTCTC GTC NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:93581886..93582029 26863196 MeRIP-seq:(Medium) rs1165830435 Functional Loss DEL dbSNP153 32..33 33 - - - 65519 RMVar_ID_65519 Human_SNP_ID_241538628 m1A Human chr5 - 93583268 93583268 93583268 AAGAAGAGAGAGAGAGAGAGAGAGAGAGACCCAAAAATTGAATGCGTTTAAACGGGAGGACTCGC AAGAAGAGAGAGAGAGAGAGAGAGAGAGACCCCAAAATTGAATGCGTTTAAACGGGAGGACTCGC T G NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93583220..93583488 26863196 MeRIP-seq:(Medium) rs1326202848 Functional Loss SNV dbSNP153 33..33 33 - - - 65520 RMVar_ID_65520 Human_SNP_ID_241538648 m1A Human chr5 - 93583300 93583295 93583300 AGAGAGAGGAGAGAGAGAGAGAGAGAGAAGAGAAGAAGAGAGAGAGAGAGAGAGAGAGAGACCCA AGAGAGAGGAGAGAGAGAGAGAGAGAGAAGAG_____GAGAGAGAGAGAGAGAGAGAGAGACCCA CTTCTT C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:93583235..93583440 26863410 MeRIP-seq:(Medium) rs1248810192 Functional Loss DEL dbSNP153 33..37 33 - - - 65521 RMVar_ID_65521 Human_SNP_ID_241538656 m1A Human chr5 - 93583300 93583300 93583300 AGAGAGAGGAGAGAGAGAGAGAGAGAGAAGAGAAGAAGAGAGAGAGAGAGAGAGAGAGAGACCCA AGAGAGAGGAGAGAGAGAGAGAGAGAGAAGAGGAGAAGAGAGAGAGAGAGAGAGAGAGAGACCCA T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:93583235..93583440 26863410 MeRIP-seq:(Medium) rs1314950855 Functional Loss SNV dbSNP153 33..33 33 - - - 65522 RMVar_ID_65522 Human_SNP_ID_241538904 m1A Human chr5 - 93584090 93584090 93584090 GGAGCGCGGTGAGCCGAGCAGGGCGCTGGGCGAGGCTGCCGCCGGCGATCAGGGCGCGCGGGTGT GGAGCGCGGTGAGCCGAGCAGGGCGCTGGGCGGGGCTGCCGCCGGCGATCAGGGCGCGCGGGTGT T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:93583997..93584114;chr5:93583667..93584625;chr5:93583810..93584646;chr5:93583801..93584650 26863196 MeRIP-seq:(Medium) rs1338392693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5215031,Human_RBP_ID_5612738 65523 RMVar_ID_65523 Human_SNP_ID_241538960 m1A Human chr5 + 93584215 93584215 93584215 CGGCCTCCGCTCGCGCTCCGGCTGCGGCCCCGACTCCTGCTCGGACTCCGGCCCGGGTCCCGGCT CGGCCTCCGCTCGCGCTCCGGCTGCGGCCCCGCCTCCTGCTCGGACTCCGGCCCGGGTCCCGGCT A C NR2F1 Ensembl:ENSG00000175745 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:93584027..93584300 26863196 MeRIP-seq:(Medium) rs1171366800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4843421 65524 RMVar_ID_65524 Human_SNP_ID_241539182 m1A Human chr5 + 93584752 93584752 93584752 CTGGGGGGGCTGCAAAAAGAGAGAAAGAAAACAGCAGGAACCACAACAAAACGCCAGCAGGGCGG CTGGGGGGGCTGCAAAAAGAGAGAAAGAAAACGGCAGGAACCACAACAAAACGCCAGCAGGGCGG A G NR2F1 Ensembl:ENSG00000175745 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:93584701..93584875;chr5:93584701..93584925 26863196 MeRIP-seq:(Medium) rs1485860040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18465202,Human_RBP_ID_22100657 65525 RMVar_ID_65525 Human_SNP_ID_241539250 m1A Human chr5 - 93584918 93584917 93584918 GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGG_GGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT CT C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr5:93584818..93584935;chr5:93584818..93584918 26863410 MeRIP-seq:(Medium) rs1274848670 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8213172,Human_RBP_ID_8268030,Human_RBP_ID_26792092 65526 RMVar_ID_65526 Human_SNP_ID_241539252 m1A Human chr5 - 93584918 93584918 93584918 GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGGGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr5:93584818..93584935;chr5:93584818..93584918 26863410 MeRIP-seq:(Medium) rs898353185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213172,Human_RBP_ID_8268030,Human_RBP_ID_26792092 65527 RMVar_ID_65527 Human_SNP_ID_241539253 m1A Human chr5 - 93584918 93584918 93584918 GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGCGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT T G NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr5:93584818..93584935;chr5:93584818..93584918 26863410 MeRIP-seq:(Medium) rs898353185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213172,Human_RBP_ID_8268030,Human_RBP_ID_26792092 65528 RMVar_ID_65528 Human_SNP_ID_241539274 m1A Human chr5 - 93584949 93584949 93584949 CCGAGGGCCGCGGGGCGCGCGGGCGCGCTGGGAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAG CCGAGGGCCGCGGGGCGCGCGGGCGCGCTGGGGGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAG T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:93584868..93585363 26863410 MeRIP-seq:(Medium) rs1389356029 Functional Loss SNV dbSNP153 33..33 33 - - - 65529 RMVar_ID_65529 Human_SNP_ID_241539312 m1A Human chr5 - 93585025 93585025 93585025 GCGGATCTCGCCAGCTGCTAACTACCATTGCCATATCTTTGGGCCCGGGGAGCGCTGGGGGGAGC GCGGATCTCGCCAGCTGCTAACTACCATTGCCGTATCTTTGGGCCCGGGGAGCGCTGGGGGGAGC T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93584976..93585126 26863196 MeRIP-seq:(Medium) rs886041216 Functional Loss SNV dbSNP153 33..33 33 - - - 65530 RMVar_ID_65530 Human_SNP_ID_241539315 m1A Human chr5 - 93585037 93585037 93585037 CCACGTCGTCCTGCGGATCTCGCCAGCTGCTAACTACCATTGCCATATCTTTGGGCCCGGGGAGC CCACGTCGTCCTGCGGATCTCGCCAGCTGCTAGCTACCATTGCCATATCTTTGGGCCCGGGGAGC T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:93584986..93585178 26863196 MeRIP-seq:(Medium) rs1468965930 Functional Loss SNV dbSNP153 33..33 33 - - - 65531 RMVar_ID_65531 Human_SNP_ID_241539432 m1A Human chr5 - 93585288 93585288 93585288 GCCGTAGTGCTTGCCGCTCGACTTGTCCCCGCACACCACGCACTCGATGTGCTGCTGGCTCTGGC GCCGTAGTGCTTGCCGCTCGACTTGTCCCCGCGCACCACGCACTCGATGTGCTGCTGGCTCTGGC T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93585239..93585389 26863196 MeRIP-seq:(Medium) rs1561523716 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_263 65532 RMVar_ID_65532 Human_SNP_ID_241540133 m1A Human chr5 + 93588084 93588082 93588085 CGTCGCGCTACGGCAGCCAGTGCATGCAGCCCAACAACATTATGGGCATCGAGAACATCTGCGAG CGTCGCGCTACGGCAGCCAGTGCATGCAGCC___CAACATTATGGGCATCGAGAACATCTGCGAG CCAA C NR2F1 Ensembl:ENSG00000175745 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:93588035..93588115 32194978 MeRIP-seq:(Medium) rs749118126 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9399244,Human_RBP_ID_18055783,Human_RBP_ID_27338979 Human_miRNA_ID_1205643 RMVar_hsa_circ_6452,RMVar_hsa_circ_233245 65533 RMVar_ID_65533 Human_SNP_ID_241561327 m1A Human chr5 - 93682884 93682884 93682884 TCAATTATGTGAAGAATTGCTTCCGGATGACTAACCAAGAGGCTATTCAAGATCTCTGGCAGTGG TCAATTATGTGAAGAATTGCTTCCGGATGACTGACCAAGAGGCTATTCAAGATCTCTGGCAGTGG T C NPM1P27,FAM172A Ensembl:ENSG00000249353,Ensembl:ENSG00000113391 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878979147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2950898,Human_RBP_ID_5611378,Human_RBP_ID_7492505,Human_RBP_ID_17416808,Human_RBP_ID_22404067 65534 RMVar_ID_65534 Human_SNP_ID_241561468 m1A Human chr5 - 93683461 93683461 93683461 CTGGCAACTTTGAAAATGTCTGTACAGCCAACAGTTTCCCTTGGGGGCTTTGAAATAACACCACC CTGGCAACTTTGAAAATGTCTGTACAGCCAACGGTTTCCCTTGGGGGCTTTGAAATAACACCACC T C NPM1P27,FAM172A Ensembl:ENSG00000249353,Ensembl:ENSG00000113391 Pseudogene,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs538281040 Functional Loss SNV dbSNP153 33..33 33 - - - 65535 RMVar_ID_65535 Human_SNP_ID_241571368 m1A Human chr5 + 93729144 93729143 93729144 GTCTGTCTTTCTCTCTCTCCTCACCTCGCTCCACTCCTAGTTATCCTTTACGTTGTTCCCCGTTC GTCTGTCTTTCTCTCTCTCCTCACCTCGCTCC_CTCCTAGTTATCCTTTACGTTGTTCCCCGTTC CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93729109..93729217 26863196 MeRIP-seq:(Medium) rs1213222203 Functional Loss DEL dbSNP153 33..33 33 - - - 65536 RMVar_ID_65536 Human_SNP_ID_241631557 m1A Human chr5 - 93985652 93985652 93985652 GGGAGGCCGAGGCGGGCAGATCACCAGAGGTCAGGAGCAGGAGACCAGCCCGGCCAACAGGGCGA GGGAGGCCGAGGCGGGCAGATCACCAGAGGTCGGGAGCAGGAGACCAGCCCGGCCAACAGGGCGA T C FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93985601..93985728 26863196 MeRIP-seq:(Medium) rs1288436070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48877,RMVar_hsa_circ_24183,RMVar_hsa_circ_314840,RMVar_hsa_circ_46771,RMVar_hsa_circ_326361,RMVar_hsa_circ_295210,RMVar_hsa_circ_275664,RMVar_hsa_circ_348576,RMVar_hsa_circ_17591,RMVar_hsa_circ_288932,RMVar_hsa_circ_273512,RMVar_hsa_circ_74164,RMVar_hsa_circ_233251,RMVar_hsa_circ_35913 65537 RMVar_ID_65537 Human_SNP_ID_241660131 m1A Human chr5 - 94111455 94111455 94111455 GTGAGCTCCGGGGGCAGGCCCGGGTCGAAATCAGGAGGGGGCTGGCCTGGGTCGGTCTCAGGCGG GTGAGCTCCGGGGGCAGGCCCGGGTCGAAATCTGGAGGGGGCTGGCCTGGGTCGGTCTCAGGCGG T A FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:94111404..94111475 26863196 MeRIP-seq:(Medium) rs182579420 Functional Loss SNV dbSNP153 33..33 33 - - - 65538 RMVar_ID_65538 Human_SNP_ID_241660132 m1A Human chr5 - 94111455 94111455 94111455 GTGAGCTCCGGGGGCAGGCCCGGGTCGAAATCAGGAGGGGGCTGGCCTGGGTCGGTCTCAGGCGG GTGAGCTCCGGGGGCAGGCCCGGGTCGAAATCGGGAGGGGGCTGGCCTGGGTCGGTCTCAGGCGG T C FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:94111404..94111475 26863196 MeRIP-seq:(Medium) rs182579420 Functional Loss SNV dbSNP153 33..33 33 - - - 65539 RMVar_ID_65539 Human_SNP_ID_241687890 m1A Human chr5 - 94242571 94242564 94242572 GAAAGGAAAGAAGGAAAGAAAAAAAGGAAGGAAGGAAGGTAGGAAGGAAGGAAAGAAAAATATAC GAAAGGAAAGAAGGAAAGAAAAAAAGGAAGG________TAGGAAGGAAGGAAAGAAAAATATAC ACCTTCCTT A KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:94242532..94242651 26863196 MeRIP-seq:(Medium) rs1028447474 Functional Loss DEL dbSNP153 32..39 33 - - - 65540 RMVar_ID_65540 Human_SNP_ID_241687891 m1A Human chr5 - 94242571 94242564 94242572 GAAAGGAAAGAAGGAAAGAAAAAAAGGAAGGAAGGAAGGTAGGAAGGAAGGAAAGAAAAATATAC GAAAGGAAAGAAGGAAAGAAAAAAAGGAAGG____AAGGTAGGAAGGAAGGAAAGAAAAATATAC ACCTTCCTT ACCTT KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:94242532..94242651 26863196 MeRIP-seq:(Medium) rs1028447474 Functional Loss DEL dbSNP153 32..35 33 - - - 65541 RMVar_ID_65541 Human_SNP_ID_241756439 m1A Human chr5 - 94565038 94565032 94565038 GAGACAGGAAAGAAAGAGAGAGAGAGAGAGAGAGGAAAGAAAGAGAGAGAGAGAGAGAGAGGGAG GAGACAGGAAAGAAAGAGAGAGAGAGAGAGAG______GAAAGAGAGAGAGAGAGAGAGAGGGAG CTTTCCT C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:94564987..94565094 26863196 MeRIP-seq:(Medium) rs1185167794 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_345493,RMVar_hsa_circ_330666,RMVar_hsa_circ_308880,RMVar_hsa_circ_233278 65542 RMVar_ID_65542 Human_SNP_ID_241756453 m1A Human chr5 - 94565038 94565038 94565038 GAGACAGGAAAGAAAGAGAGAGAGAGAGAGAGAGGAAAGAAAGAGAGAGAGAGAGAGAGAGGGAG GAGACAGGAAAGAAAGAGAGAGAGAGAGAGAGGGGAAAGAAAGAGAGAGAGAGAGAGAGAGGGAG T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:94564987..94565094 26863196 MeRIP-seq:(Medium) rs539307306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345493,RMVar_hsa_circ_330666,RMVar_hsa_circ_308880,RMVar_hsa_circ_233278 65543 RMVar_ID_65543 Human_SNP_ID_241757559 m1A Human chr5 + 94569445 94569445 94569445 CCCCACAAACCCCATTACTAAAACCACACTTAACAAAAATAAAGCATATGTCATTATTCTCGCAC CCCCACAAACCCCATTACTAAAACCACACTTAGCAAAAATAAAGCATATGTCATTATTCTCGCAC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:94569345..94569525 26863410 MeRIP-seq:(Medium) rs1366514748 Functional Loss SNV dbSNP153 33..33 33 - - - 65544 RMVar_ID_65544 Human_SNP_ID_241757821 m1A Human chr5 - 94570285 94570277 94570285 TAGTCAGGGTGTAGTTGTCTGGGTCGCCCAGGAGGTCTGGTGAGAATAGTACTAGTGTTAATAGG TAGTCAGGGTGTAGTTGTCTGGGTCGCCCAGG________TGAGAATAGTACTAGTGTTAATAGG ACCAGACCT A KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:94570259..94570370 26863196 MeRIP-seq:(Medium) rs1334972505 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_7487293,Human_RBP_ID_27745715 RMVar_hsa_circ_345493,RMVar_hsa_circ_330666,RMVar_hsa_circ_308880,RMVar_hsa_circ_233278 65545 RMVar_ID_65545 Human_SNP_ID_241757822 m1A Human chr5 - 94570285 94570285 94570285 TAGTCAGGGTGTAGTTGTCTGGGTCGCCCAGGAGGTCTGGTGAGAATAGTACTAGTGTTAATAGG TAGTCAGGGTGTAGTTGTCTGGGTCGCCCAGGTGGTCTGGTGAGAATAGTACTAGTGTTAATAGG T A KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:94570259..94570370 26863196 MeRIP-seq:(Medium) rs1444394811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7487293,Human_RBP_ID_27745715 RMVar_hsa_circ_345493,RMVar_hsa_circ_330666,RMVar_hsa_circ_308880,RMVar_hsa_circ_233278 65546 RMVar_ID_65546 Human_SNP_ID_241778221 m1A Human chr5 + 94653286 94653286 94653286 TGGTCTAAATACATGTAGAAGGAAATTAAGAAAAAAGATGAAGATATTCAGAGGAGTTATACTTT TGGTCTAAATACATGTAGAAGGAAATTAAGAACAAAGATGAAGATATTCAGAGGAGTTATACTTT A C SLF1 Ensembl:ENSG00000133302 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:94653251..94653300 26863196 MeRIP-seq:(Medium) rs142724600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2952989,Human_RBP_ID_9182437,Human_RBP_ID_27517824 Human_Splice_Rec_674110,Human_Splice_Rec_674148 RMVar_hsa_circ_102,RMVar_hsa_circ_41290,RMVar_hsa_circ_88617,RMVar_hsa_circ_233280,RMVar_hsa_circ_292971,RMVar_hsa_circ_341114,RMVar_hsa_circ_341124,RMVar_hsa_circ_329633,RMVar_hsa_circ_308369,RMVar_hsa_circ_285325,RMVar_hsa_circ_64601,RMVar_hsa_circ_233282,RMVar_hsa_circ_233284,RMVar_hsa_circ_233283,RMVar_hsa_circ_233281,RMVar_hsa_circ_6602,RMVar_hsa_circ_233291,RMVar_hsa_circ_272009,RMVar_hsa_circ_330834,RMVar_hsa_circ_321241,RMVar_hsa_circ_68668,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_314936,RMVar_hsa_circ_340996,RMVar_hsa_circ_310749,RMVar_hsa_circ_42836,RMVar_hsa_circ_63127,RMVar_hsa_circ_69299,RMVar_hsa_circ_233293,RMVar_hsa_circ_233294,RMVar_hsa_circ_50588,RMVar_hsa_circ_369864,RMVar_hsa_circ_233295,RMVar_hsa_circ_60996 65547 RMVar_ID_65547 Human_SNP_ID_241793651 m1A Human chr5 - 94714726 94714726 94714726 TGAGCCCCATTCTTCTGTGGGATAAGGTGTCCATTTGTTTCTTGGAGGGTGAAATGCCACATTCT TGAGCCCCATTCTTCTGTGGGATAAGGTGTCCGTTTGTTTCTTGGAGGGTGAAATGCCACATTCT T C MCTP1 Ensembl:ENSG00000175471 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:94714675..94714824 26863196 MeRIP-seq:(Medium) rs1212063934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73977 65548 RMVar_ID_65548 Human_SNP_ID_241793658 m1A Human chr5 + 94714741 94714741 94714741 ACCCTCCAAGAAACAAATGGACACCTTATCCCACAGAAGAATGGGGCTCACAGGTCACCGTCACT ACCCTCCAAGAAACAAATGGACACCTTATCCCCCAGAAGAATGGGGCTCACAGGTCACCGTCACT A C SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:94714701..94714789 26863196 MeRIP-seq:(Medium) rs1478259108 Functional Loss SNV dbSNP153 33..33 33 - - - 65549 RMVar_ID_65549 Human_SNP_ID_241983456 m1A Human chr5 - 95534289 95534289 95534289 AGGTGAGATAGTTAACATTATGAGAGTGTTGCACTGAGGCTGAGGAGGATGAGGTACATCAAGCA AGGTGAGATAGTTAACATTATGAGAGTGTTGCCCTGAGGCTGAGGAGGATGAGGTACATCAAGCA T G TTC37 Ensembl:ENSG00000198677 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:95534264..95534437 26863196 MeRIP-seq:(Medium) rs1427691723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7488681,Human_RBP_ID_15550161 RMVar_hsa_circ_88669,RMVar_hsa_circ_233333,RMVar_hsa_circ_95131,RMVar_hsa_circ_233337,RMVar_hsa_circ_104951,RMVar_hsa_circ_233352,RMVar_hsa_circ_233355,RMVar_hsa_circ_115353,RMVar_hsa_circ_233357,RMVar_hsa_circ_97818,RMVar_hsa_circ_99415,RMVar_hsa_circ_95144,RMVar_hsa_circ_233359,RMVar_hsa_circ_233360,RMVar_hsa_circ_233358,RMVar_hsa_circ_77327,RMVar_hsa_circ_22650,RMVar_hsa_circ_103179,RMVar_hsa_circ_233361,RMVar_hsa_circ_105776,RMVar_hsa_circ_233365,RMVar_hsa_circ_29161,RMVar_hsa_circ_233364,RMVar_hsa_circ_351182,RMVar_hsa_circ_49398,RMVar_hsa_circ_67872,RMVar_hsa_circ_22053,RMVar_hsa_circ_72825,RMVar_hsa_circ_374728,RMVar_hsa_circ_233367 65550 RMVar_ID_65550 Human_SNP_ID_241987039 m1A Human chr5 - 95550636 95550636 95550636 TGTTTTTGTTTAATTTAGATGGAAAATGGGTAAGGAACAATCAAATTCAATTCGGGAAGAATATA TGTTTTTGTTTAATTTAGATGGAAAATGGGTAGGGAACAATCAAATTCAATTCGGGAAGAATATA T C TTC37 Ensembl:ENSG00000198677 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:95550576..95550675 26863196 MeRIP-seq:(Medium) rs556033488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1043174,Human_RBP_ID_2953635,Human_RBP_ID_23050147,Human_RBP_ID_25945361,Human_RBP_ID_26351061,Human_RBP_ID_27825605 Human_Splice_Rec_674626,Human_Splice_Rec_674627,Human_Splice_Rec_674710,Human_Splice_Rec_674711,Human_Splice_Rec_674876,Human_Splice_Rec_674877,Human_Splice_Rec_674928,Human_Splice_Rec_674929,Human_Splice_Rec_674937 RMVar_hsa_circ_97818,RMVar_hsa_circ_95144,RMVar_hsa_circ_233359,RMVar_hsa_circ_233360,RMVar_hsa_circ_72825,RMVar_hsa_circ_65250,RMVar_hsa_circ_8151 65551 RMVar_ID_65551 Human_SNP_ID_241988121 m1A Human chr5 - 95555188 95555186 95555189 TCCCTAGCAGAGCAGGGCAGGGACAGCGAACAACTCCCAAAGCTTGCAGTTTGGTTGCTTGATAG TCCCTAGCAGAGCAGGGCAGGGACAGCGAAC___TCCCAAAGCTTGCAGTTTGGTTGCTTGATAG AGTT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:95555139..95555225 26863196 MeRIP-seq:(Medium) rs1470129761 Functional Loss DEL dbSNP153 32..34 33 - - - 65552 RMVar_ID_65552 Human_SNP_ID_242008858 m1A Human chr5 + 95646817 95646817 95646817 GTCACGCGGAGGCGGAGCGAGGACTCGGGGACAGTAAGTTCTGTTCTCGCCGCGCAGGGGGCGGG GTCACGCGGAGGCGGAGCGAGGACTCGGGGACGGTAAGTTCTGTTCTCGCCGCGCAGGGGGCGGG A G RFESD Ensembl:ENSG00000175449 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:95646795..95646866 26863196 MeRIP-seq:(Medium) rs1253778395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_674995,Human_Splice_Rec_675003,Human_Splice_Rec_675005 65553 RMVar_ID_65553 Human_SNP_ID_242027682 m1A Human chr5 + 95731342 95731330 95731343 AGAGGAGGAGGAGCAGCGGCAGCGGCAGCAGGAGGCGACAGCTGCCAGCCGAGGAGGCGCGGCGG AGAGGAGGAGGAGCAGCGGCA_____________GCGACAGCTGCCAGCCGAGGAGGCGCGGCGG AGCGGCAGCAGGAG A RHOBTB3 Ensembl:ENSG00000164292 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:95731151..95731589 26863196 MeRIP-seq:(Medium) rs1394570344 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_4845846,Human_RBP_ID_5326802,Human_RBP_ID_8943839,Human_RBP_ID_9335260 65554 RMVar_ID_65554 Human_SNP_ID_242027808 m1A Human chr5 - 95731647 95731647 95731647 CTCAAATCCAAGGGCAGGGCGGCGACTCGGAGAAAAGCAGCGGCTCACGGCTTCGCGGGGCCCCC CTCAAATCCAAGGGCAGGGCGGCGACTCGGAGGAAAGCAGCGGCTCACGGCTTCGCGGGGCCCCC T C AC008840.1 Ensembl:ENSG00000250240 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:95731597..95731788 26863196 MeRIP-seq:(Medium) rs956723170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5302785 65555 RMVar_ID_65555 Human_SNP_ID_242028033 m1A Human chr5 - 95732086 95732085 95732086 TCAGCCTCAGCGCGGAGCAGCTGCTCTTCCTTACCCAGACGGGACAGTCGTGGACCACCAGCTTG TCAGCCTCAGCGCGGAGCAGCTGCTCTTCCTT_CCCAGACGGGACAGTCGTGGACCACCAGCTTG GT G AC008840.1 Ensembl:ENSG00000250240 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:95732036..95732152 32194978 MeRIP-seq:(Medium) rs772329551 Functional Loss DEL dbSNP153 33..33 33 - - - 65556 RMVar_ID_65556 Human_SNP_ID_242039128 m1A Human chr5 + 95780302 95780302 95780302 ACAGGGCCATCCTGGTGGCCCGTTGTGAAGTGATGGCAGCCATGTTTAATGGTAATTACATGGAA ACAGGGCCATCCTGGTGGCCCGTTGTGAAGTGTTGGCAGCCATGTTTAATGGTAATTACATGGAA A T RHOBTB3 Ensembl:ENSG00000164292 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:95780251..95780450 32194978 MeRIP-seq:(Medium) rs376618967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8893175,Human_RBP_ID_9307019,Human_RBP_ID_25932739 Human_Splice_Rec_675164,Human_Splice_Rec_675186,Human_Splice_Rec_675194 RMVar_hsa_circ_206,RMVar_hsa_circ_233372,RMVar_hsa_circ_117758,RMVar_hsa_circ_94185,RMVar_hsa_circ_233371,RMVar_hsa_circ_313991,RMVar_hsa_circ_274478,RMVar_hsa_circ_27664,RMVar_hsa_circ_233374,RMVar_hsa_circ_233373,RMVar_hsa_circ_349183,RMVar_hsa_circ_289185,RMVar_hsa_circ_271944,RMVar_hsa_circ_27314,RMVar_hsa_circ_76091,RMVar_hsa_circ_233386,RMVar_hsa_circ_233387,RMVar_hsa_circ_233385,RMVar_hsa_circ_361640,RMVar_hsa_circ_325247,RMVar_hsa_circ_283792,RMVar_hsa_circ_233389,RMVar_hsa_circ_300632,RMVar_hsa_circ_111348,RMVar_hsa_circ_233391,RMVar_hsa_circ_233392,RMVar_hsa_circ_285532,RMVar_hsa_circ_233390,RMVar_hsa_circ_270072,RMVar_hsa_circ_33587,RMVar_hsa_circ_233398,RMVar_hsa_circ_59253,RMVar_hsa_circ_233397,RMVar_hsa_circ_233399,RMVar_hsa_circ_296977,RMVar_hsa_circ_276177,RMVar_hsa_circ_233401,RMVar_hsa_circ_233402,RMVar_hsa_circ_56968 65557 RMVar_ID_65557 Human_SNP_ID_242051973 m1A Human chr5 + 95835031 95835031 95835031 AATGTCCTCATCCGGGCCCGGGACGTCCCTGCAGCCCAAGTTCGCCATGTCCCACTGCTGCCTGC AATGTCCTCATCCGGGCCCGGGACGTCCCTGCCGCCCAAGTTCGCCATGTCCCACTGCTGCCTGC A C LOC102724720 RNACentral:URS0000D78032 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:95834983..95835112 26863196 MeRIP-seq:(Medium) rs778154371 Functional Loss SNV dbSNP153 33..33 33 - - - 65558 RMVar_ID_65558 Human_SNP_ID_242076410 m1A Human chr5 - 95940843 95940843 95940843 CGCAGGGCCACCGATGTGAGGGTCTTCTGTACACTGCTCCTCTGTTTTTCTCGAGAGCCATGATA CGCAGGGCCACCGATGTGAGGGTCTTCTGTACGCTGCTCCTCTGTTTTTCTCGAGAGCCATGATA T C ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:95940841..95940957 32194978 MeRIP-seq:(Medium) rs150038873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7489504 RMVar_hsa_circ_27913,RMVar_hsa_circ_342847 65559 RMVar_ID_65559 Human_SNP_ID_242076894 m1A Human chr5 - 95943048 95943048 95943048 ACCTGTTTGTTTCTTTTGTTTCTTTTAATAGAATTTAATTCCTTTTCGACCTTCAATCCAGTTCC ACCTGTTTGTTTCTTTTGTTTCTTTTAATAGATTTTAATTCCTTTTCGACCTTCAATCCAGTTCC T A ELL2 Ensembl:ENSG00000118985 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:95943016..95943129 26863196 MeRIP-seq:(Medium) rs766254959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3782229 Human_Splice_Rec_675264,Human_Splice_Rec_675265,Human_Splice_Rec_675290,Human_Splice_Rec_675291,Human_Splice_Rec_675300,Human_Splice_Rec_675301,Human_Splice_Rec_675303,Human_Splice_Rec_675308,Human_Splice_Rec_675309,Human_Splice_Rec_675316 RMVar_hsa_circ_27913,RMVar_hsa_circ_342847 65560 RMVar_ID_65560 Human_SNP_ID_242080693 m1A Human chr5 - 95959710 95959710 95959710 TCAGGGAGGAGTGCATGCACAGGGAGAAAGGTACCGTCCTACATACAGTGAAATCTCGAGAGAAA TCAGGGAGGAGTGCATGCACAGGGAGAAAGGTTCCGTCCTACATACAGTGAAATCTCGAGAGAAA T A ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:95959706..95959771 26863196 MeRIP-seq:(Medium) rs559538328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21945093,Human_RBP_ID_21989646,Human_RBP_ID_22702600 65561 RMVar_ID_65561 Human_SNP_ID_242127935 m1A Human chr5 + 96171027 96171027 96171027 GTCCGTAGAAAAGGAAGATTGGAGACTCCGCGACGCTTGGGGTTGGGACTGAGGGGACAGGTGGG GTCCGTAGAAAAGGAAGATTGGAGACTCCGCGGCGCTTGGGGTTGGGACTGAGGGGACAGGTGGG A G AC104123.1,MIR583HG Ensembl:ENSG00000251314,Ensembl:ENSG00000250551 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:96170907..96171140 26863196 MeRIP-seq:(Medium) rs1301810570 Functional Loss SNV dbSNP153 33..33 33 - - - 65562 RMVar_ID_65562 Human_SNP_ID_242127936 m1A Human chr5 + 96171027 96171027 96171027 GTCCGTAGAAAAGGAAGATTGGAGACTCCGCGACGCTTGGGGTTGGGACTGAGGGGACAGGTGGG GTCCGTAGAAAAGGAAGATTGGAGACTCCGCGTCGCTTGGGGTTGGGACTGAGGGGACAGGTGGG A T AC104123.1,MIR583HG Ensembl:ENSG00000251314,Ensembl:ENSG00000250551 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:96170907..96171140 26863196 MeRIP-seq:(Medium) rs1301810570 Functional Loss SNV dbSNP153 33..33 33 - - - 65563 RMVar_ID_65563 Human_SNP_ID_242183219 m1A Human chr5 + 96408255 96408255 96408255 TTTGCTTCCAGGGCCAGAGCGAAGATGCCAGCAGCCAGAGGTGCAGAGGCCGAGGTGCCTGTGTG TTTGCTTCCAGGGCCAGAGCGAAGATGCCAGCGGCCAGAGGTGCAGAGGCCGAGGTGCCTGTGTG A G AC104123.1 Ensembl:ENSG00000251314 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:96408188..96408266 26863196 MeRIP-seq:(Medium) rs769697467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5613997 65564 RMVar_ID_65564 Human_SNP_ID_242246072 m1A Human chr5 + 96662402 96662402 96662402 CCCGCCACTCTCCGCGGCGCATTCCGGGAGGCAGCGGCCGCAGCGGCCTCGCCATGTCCCAGCCC CCCGCCACTCTCCGCGGCGCATTCCGGGAGGCGGCGGCCGCAGCGGCCTCGCCATGTCCCAGCCC A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:96662351..96662500 26863196 MeRIP-seq:(Medium) rs1471748216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846528 Human_Splice_Rec_675504,Human_Splice_Rec_675505,Human_Splice_Rec_675565,Human_Splice_Rec_675593,Human_Splice_Rec_675651,Human_Splice_Rec_675655,Human_Splice_Rec_675663,Human_Splice_Rec_675687,Human_Splice_Rec_675745,Human_Splice_Rec_675749 65565 RMVar_ID_65565 Human_SNP_ID_242246079 m1A Human chr5 + 96662423 96662423 96662423 TTCCGGGAGGCAGCGGCCGCAGCGGCCTCGCCATGTCCCAGCCCGGCCAGAAGCCCGCCGCCTCC TTCCGGGAGGCAGCGGCCGCAGCGGCCTCGCCCTGTCCCAGCCCGGCCAGAAGCCCGCCGCCTCC A C CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:96662376..96662553 26863196 MeRIP-seq:(Medium) rs878906668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4844123 Human_Splice_Rec_675504,Human_Splice_Rec_675505,Human_Splice_Rec_675565,Human_Splice_Rec_675593,Human_Splice_Rec_675651,Human_Splice_Rec_675655,Human_Splice_Rec_675663,Human_Splice_Rec_675687,Human_Splice_Rec_675745,Human_Splice_Rec_675749 65566 RMVar_ID_65566 Human_SNP_ID_242246080 m1A Human chr5 + 96662423 96662423 96662423 TTCCGGGAGGCAGCGGCCGCAGCGGCCTCGCCATGTCCCAGCCCGGCCAGAAGCCCGCCGCCTCC TTCCGGGAGGCAGCGGCCGCAGCGGCCTCGCCGTGTCCCAGCCCGGCCAGAAGCCCGCCGCCTCC A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:96662376..96662553 26863196 MeRIP-seq:(Medium) rs878906668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4844123 Human_Splice_Rec_675504,Human_Splice_Rec_675505,Human_Splice_Rec_675565,Human_Splice_Rec_675593,Human_Splice_Rec_675651,Human_Splice_Rec_675655,Human_Splice_Rec_675663,Human_Splice_Rec_675687,Human_Splice_Rec_675745,Human_Splice_Rec_675749 65567 RMVar_ID_65567 Human_SNP_ID_242246125 m1A Human chr5 + 96662493 96662493 96662493 GCCCCGGCGAGCAGCCGCCGCCCGCCGCACCCATGAGGTGAGTGGCGCTCCTGTCGGCGTCGCGG GCCCCGGCGAGCAGCCGCCGCCCGCCGCACCCGTGAGGTGAGTGGCGCTCCTGTCGGCGTCGCGG A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:96662376..96662517 26863196 MeRIP-seq:(Medium) rs1360411376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_675505,Human_Splice_Rec_675565,Human_Splice_Rec_675593,Human_Splice_Rec_675651,Human_Splice_Rec_675655,Human_Splice_Rec_675663,Human_Splice_Rec_675687,Human_Splice_Rec_675745,Human_Splice_Rec_675749 65568 RMVar_ID_65568 Human_SNP_ID_242249312 m1A Human chr5 - 96675529 96675528 96675529 TCACTGGTTTTTTCACTGACATGCTATAAAAAAGTAAAAAATAATGCTTAATAAAGGAAGATGAC TCACTGGTTTTTTCACTGACATGCTATAAAAA_GTAAAAAATAATGCTTAATAAAGGAAGATGAC CT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:96675526..96675600 26863196 MeRIP-seq:(Medium) rs763376823 Functional Loss DEL dbSNP153 33..33 33 - - - 65569 RMVar_ID_65569 Human_SNP_ID_242249338 m1A Human chr5 + 96675588 96675588 96675588 CAGTGAATCGCCTTCCAAACCAGGAGAAAAGAAAGGATCAGATGAGGTAATTTCCACAATACTGG CAGTGAATCGCCTTCCAAACCAGGAGAAAAGAGAGGATCAGATGAGGTAATTTCCACAATACTGG A G CAST Ensembl:ENSG00000153113 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:96675526..96675625 26863196 MeRIP-seq:(Medium) rs762055986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9398008 Human_Splice_Rec_675422,Human_Splice_Rec_675423,Human_Splice_Rec_675444,Human_Splice_Rec_675445,Human_Splice_Rec_675506,Human_Splice_Rec_675507,Human_Splice_Rec_675566,Human_Splice_Rec_675567,Human_Splice_Rec_675594,Human_Splice_Rec_675595,Human_Splice_Rec_675652,Human_Splice_Rec_675653,Human_Splice_Rec_675656,Human_Splice_Rec_675657,Human_Splice_Rec_675664,Human_Splice_Rec_675665,Human_Splice_Rec_675688,Human_Splice_Rec_675689,Human_Splice_Rec_675746,Human_Splice_Rec_675747,Human_Splice_Rec_675750,Human_Splice_Rec_675751,Human_Splice_Rec_675774,Human_Splice_Rec_675775,Human_Splice_Rec_675786,Human_Splice_Rec_675788,Human_Splice_Rec_675789,Human_Splice_Rec_675802,Human_Splice_Rec_675803,Human_Splice_Rec_675814,Human_Splice_Rec_675815 RMVar_hsa_circ_4726 65570 RMVar_ID_65570 Human_SNP_ID_242253840 m1A Human chr5 + 96695838 96695838 96695838 CCATTGAAACTAATATTTTCTATTTTCAAGAAAAAAGCAGCAAGCCTCGGCAGCAGTCAATCCTC CCATTGAAACTAATATTTTCTATTTTCAAGAAGAAAGCAGCAAGCCTCGGCAGCAGTCAATCCTC A G CAST Ensembl:ENSG00000153113 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:96695826..96695875 26863196 MeRIP-seq:(Medium) rs1463333322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_675424,Human_Splice_Rec_675425,Human_Splice_Rec_675446,Human_Splice_Rec_675447,Human_Splice_Rec_675508,Human_Splice_Rec_675509,Human_Splice_Rec_675568,Human_Splice_Rec_675569,Human_Splice_Rec_675596,Human_Splice_Rec_675597,Human_Splice_Rec_675654,Human_Splice_Rec_675658,Human_Splice_Rec_675659,Human_Splice_Rec_675666,Human_Splice_Rec_675667,Human_Splice_Rec_675690,Human_Splice_Rec_675691,Human_Splice_Rec_675752,Human_Splice_Rec_675753,Human_Splice_Rec_675776,Human_Splice_Rec_675777,Human_Splice_Rec_675790,Human_Splice_Rec_675791,Human_Splice_Rec_675804,Human_Splice_Rec_675805,Human_Splice_Rec_675816,Human_Splice_Rec_675817,Human_Splice_Rec_675873,Human_Splice_Rec_675931 RMVar_hsa_circ_4726,RMVar_hsa_circ_233414,RMVar_hsa_circ_83633,RMVar_hsa_circ_341193 65571 RMVar_ID_65571 Human_SNP_ID_242253852 m1A Human chr5 - 96695866 96695866 96695866 CGAGGCTGTTCCACCAGCATAGGTTCTGGAGGATTGACTGCTGCCGAGGCTTGCTGCTTTTTTCT CGAGGCTGTTCCACCAGCATAGGTTCTGGAGGGTTGACTGCTGCCGAGGCTTGCTGCTTTTTTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:96695831..96695932 32194978 MeRIP-seq:(Medium) rs772148373 Functional Loss SNV dbSNP153 33..33 33 - - - 65572 RMVar_ID_65572 Human_SNP_ID_242255452 m1A Human chr5 - 96702862 96702862 96702862 GCAGTCCTCGGCTTGGTTTTCAGGAGGTCTGCATTCCTAGCTGGGCTCGGCTCCCGCGGTTTCCG GCAGTCCTCGGCTTGGTTTTCAGGAGGTCTGCGTTCCTAGCTGGGCTCGGCTCCCGCGGTTTCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:96702857..96702977 26863196 MeRIP-seq:(Medium) rs1312600481 Functional Loss SNV dbSNP153 33..33 33 - - - 65573 RMVar_ID_65573 Human_SNP_ID_242261296 m1A Human chr5 + 96729570 96729570 96729570 GTATTATGTTTAAGACTACCATCTTGTTAACAATGTCTTTATATGTGTGTGGGCACCTGTGTGTG GTATTATGTTTAAGACTACCATCTTGTTAACAGTGTCTTTATATGTGTGTGGGCACCTGTGTGTG A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:96729568..96729684 26863196 MeRIP-seq:(Medium) rs1355639458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944417,Human_RBP_ID_22681575,Human_RBP_ID_24508870 RMVar_hsa_circ_119785,RMVar_hsa_circ_14318,RMVar_hsa_circ_233414,RMVar_hsa_circ_83633,RMVar_hsa_circ_341193,RMVar_hsa_circ_273639,RMVar_hsa_circ_310823,RMVar_hsa_circ_360555,RMVar_hsa_circ_53712,RMVar_hsa_circ_233415,RMVar_hsa_circ_233416,RMVar_hsa_circ_233417,RMVar_hsa_circ_351823,RMVar_hsa_circ_53327,RMVar_hsa_circ_347412,RMVar_hsa_circ_233419,RMVar_hsa_circ_103172,RMVar_hsa_circ_233418 65574 RMVar_ID_65574 Human_SNP_ID_242261312 m1A Human chr5 - 96729606 96729606 96729606 TGATGCCTGCTTGGGTAGGCTTTTTGGCTGAAAGTACACACACAGGTGCCCACACACATATAAAG TGATGCCTGCTTGGGTAGGCTTTTTGGCTGAAGGTACACACACAGGTGCCCACACACATATAAAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:96729601..96729650 26863196 MeRIP-seq:(Medium) rs756582052 Functional Loss SNV dbSNP153 33..33 33 - - - 65575 RMVar_ID_65575 Human_SNP_ID_242267599 m1A Human chr5 + 96754608 96754608 96754608 ACCTCAAATCTAGTCACTCAGGCATGAATTTTATGGAGAGAAAAAAACATGCTAACAATGAAAAT ACCTCAAATCTAGTCACTCAGGCATGAATTTTGTGGAGAGAAAAAAACATGCTAACAATGAAAAT A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:96754607..96754756 26863196 MeRIP-seq:(Medium) rs757144996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308284,RMVar_hsa_circ_233419,RMVar_hsa_circ_103172,RMVar_hsa_circ_31939,RMVar_hsa_circ_345602,RMVar_hsa_circ_355192 65576 RMVar_ID_65576 Human_SNP_ID_242267600 m1A Human chr5 + 96754608 96754608 96754608 ACCTCAAATCTAGTCACTCAGGCATGAATTTTATGGAGAGAAAAAAACATGCTAACAATGAAAAT ACCTCAAATCTAGTCACTCAGGCATGAATTTTTTGGAGAGAAAAAAACATGCTAACAATGAAAAT A T CAST Ensembl:ENSG00000153113 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:96754607..96754756 26863196 MeRIP-seq:(Medium) rs757144996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308284,RMVar_hsa_circ_233419,RMVar_hsa_circ_103172,RMVar_hsa_circ_31939,RMVar_hsa_circ_345602,RMVar_hsa_circ_355192 65577 RMVar_ID_65577 Human_SNP_ID_242279724 m1A Human chr5 + 96803622 96803622 96803622 CTCCAGCTCCCTTCCTGAGGGTGGCCCTAGATATCTGCAGGTGGTGACTATGCAGGATGATGGTG CTCCAGCTCCCTTCCTGAGGGTGGCCCTAGATGTCTGCAGGTGGTGACTATGCAGGATGATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:96803572..96803652 26863196 MeRIP-seq:(Medium) rs1449075742 Functional Loss SNV dbSNP153 33..33 33 - - - 65578 RMVar_ID_65578 Human_SNP_ID_242312398 m1A Human chr5 - 96935391 96935391 96935391 GTGTTTTCGGCAGAGATGCCCGCCCGCATCAGAGTGCCTCAGGAGGGCGGTGAGGAGGAGACGGA GTGTTTTCGGCAGAGATGCCCGCCCGCATCAGGGTGCCTCAGGAGGGCGGTGAGGAGGAGACGGA T C AC009126.1 Ensembl:ENSG00000247121 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:96935351..96935512 26863196 MeRIP-seq:(Medium) rs533731645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612935 65579 RMVar_ID_65579 Human_SNP_ID_242312399 m1A Human chr5 - 96935391 96935391 96935391 GTGTTTTCGGCAGAGATGCCCGCCCGCATCAGAGTGCCTCAGGAGGGCGGTGAGGAGGAGACGGA GTGTTTTCGGCAGAGATGCCCGCCCGCATCAGCGTGCCTCAGGAGGGCGGTGAGGAGGAGACGGA T G AC009126.1 Ensembl:ENSG00000247121 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:96935351..96935512 26863196 MeRIP-seq:(Medium) rs533731645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612935 65580 RMVar_ID_65580 Human_SNP_ID_242312529 m1A Human chr5 - 96935782 96935782 96935782 CAGTCACTCAACAAATGTGGAGCCCTACTGCGACCCGCCCGATCCCGGACGCCGAGACACCCGCA CAGTCACTCAACAAATGTGGAGCCCTACTGCGGCCCGCCCGATCCCGGACGCCGAGACACCCGCA T C AC009126.1 Ensembl:ENSG00000247121 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:96935735..96935806 26863196 MeRIP-seq:(Medium) rs1431362856 Functional Loss SNV dbSNP153 33..33 33 - - - 65581 RMVar_ID_65581 Human_SNP_ID_242369196 m1A Human chr5 + 97179180 97179180 97179180 TCAAACTGCCGGGAACAATTTCATGGTTCTTCATGCCCATTTCAACCTGAAATTAAAGGAATCAT TCAAACTGCCGGGAACAATTTCATGGTTCTTCCTGCCCATTTCAACCTGAAATTAAAGGAATCAT A C LIX1-AS1 Ensembl:ENSG00000251513 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:97179131..97179249 26863196 MeRIP-seq:(Medium) rs779374505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312757 65582 RMVar_ID_65582 Human_SNP_ID_242369197 m1A Human chr5 + 97179180 97179180 97179180 TCAAACTGCCGGGAACAATTTCATGGTTCTTCATGCCCATTTCAACCTGAAATTAAAGGAATCAT TCAAACTGCCGGGAACAATTTCATGGTTCTTCGTGCCCATTTCAACCTGAAATTAAAGGAATCAT A G LIX1-AS1 Ensembl:ENSG00000251513 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:97179131..97179249 26863196 MeRIP-seq:(Medium) rs779374505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312757 65583 RMVar_ID_65583 Human_SNP_ID_242370609 m1A Human chr5 + 97183136 97183136 97183136 ACAGGAACGGCGGGTTTCTTACCGCGGTCAAGACCCTGAAGTCATCTCGGCTCATGTAACGCAAC ACAGGAACGGCGGGTTTCTTACCGCGGTCAAGGCCCTGAAGTCATCTCGGCTCATGTAACGCAAC A G LIX1-AS1 Ensembl:ENSG00000251513 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:97183127..97183225 26863196 MeRIP-seq:(Medium) rs1368636532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312757 65584 RMVar_ID_65584 Human_SNP_ID_242778522 m1A Human chr5 + 98770613 98770613 98770613 TCTTCTCTCACACCCAGGTCCTGCGTGTTCCGAAGTTCAGGGGCCCCCTGATCCCGCTGAGCCCC TCTTCTCTCACACCCAGGTCCTGCGTGTTCCGCAGTTCAGGGGCCCCCTGATCCCGCTGAGCCCC A C RGMB Ensembl:ENSG00000174136 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:98769428..98770654 32194978 MeRIP-seq:(Medium) rs1213033235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250932,Human_RBP_ID_4844727 Human_Splice_Rec_677296,Human_Splice_Rec_677297,Human_Splice_Rec_677305,Human_Splice_Rec_677310,Human_Splice_Rec_677311,Human_Splice_Rec_677316,Human_Splice_Rec_677317 RMVar_hsa_circ_44874,RMVar_hsa_circ_128011,RMVar_hsa_circ_233460 65585 RMVar_ID_65585 Human_SNP_ID_242781102 m1A Human chr5 + 98779726 98779726 98779726 CCTTGCGTGCCTATGCTGGCTGCACCCAGCGAACTTCAAAAGCCTGCCGTGGCAACCTGGTATAC CCTTGCGTGCCTATGCTGGCTGCACCCAGCGAGCTTCAAAAGCCTGCCGTGGCAACCTGGTATAC A G RGMB Ensembl:ENSG00000174136 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:98779676..98779800 32194978 MeRIP-seq:(Medium) rs773852734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_945391,Human_RBP_ID_1043229,Human_RBP_ID_1660177,Human_RBP_ID_27085564,Human_RBP_ID_27339090 Human_miRNA_ID_2359313 RMVar_hsa_circ_44874,RMVar_hsa_circ_128011,RMVar_hsa_circ_118066,RMVar_hsa_circ_233460,RMVar_hsa_circ_304195,RMVar_hsa_circ_233461 65586 RMVar_ID_65586 Human_SNP_ID_242784524 m1A Human chr5 - 98793464 98793464 98793464 TCTCCAGTGTGTAGCCAGGCCAGGCCTGCACCAAGGAGGTGCGAGGCAGGCTGTGTCCCAGGATG TCTCCAGTGTGTAGCCAGGCCAGGCCTGCACCGAGGAGGTGCGAGGCAGGCTGTGTCCCAGGATG T C AC008522.1 Ensembl:ENSG00000279232 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:98793126..98793525 32194978 MeRIP-seq:(Medium) rs1439177438 Functional Loss SNV dbSNP153 33..33 33 - - - 65587 RMVar_ID_65587 Human_SNP_ID_242798878 m1A Human chr5 - 98856032 98856032 98856032 TCAGTGATTTTAGACTGACCTCCATTTAAATTATGTTTATATATGAACTTTACTCTGACCTGTGA TCAGTGATTTTAGACTGACCTCCATTTAAATTGTGTTTATATATGAACTTTACTCTGACCTGTGA T C CHD1 Ensembl:ENSG00000153922 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2455425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2954742,Human_RBP_ID_8625750,Human_RBP_ID_23052547,Human_RBP_ID_24508979,Human_RBP_ID_25931461,Human_RBP_ID_26531240 GWAS_ID_7905,GWAS_ID_7906,GWAS_ID_7907,GWAS_ID_7908,GWAS_ID_7909,GWAS_ID_7910,GWAS_ID_7911,GWAS_ID_7912 65588 RMVar_ID_65588 Human_SNP_ID_242818186 m1A Human chr5 + 98928402 98928402 98928402 ACGCCCCCTGCGCGCCAGGCCCGTACACCGCCACCGGCACTCACAGAGCCACCCGGCCTTCACCC ACGCCCCCTGCGCGCCAGGCCCGTACACCGCCCCCGGCACTCACAGAGCCACCCGGCCTTCACCC A C LINC02062,LINC02062:2,LINC02062:3 RNACentral:URS0000D5D71D,RNACentral:URS0000D5D3CF,RNACentral:URS0000D5C79C lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:98928400..98928473 26863196 MeRIP-seq:(Medium) rs1176089618 Functional Loss SNV dbSNP153 33..33 33 - - - 65589 RMVar_ID_65589 Human_SNP_ID_242818423 m1A Human chr5 - 98928806 98928806 98928806 GCGCGCGCGCGACGGCGGCGGCGGCGGCGGCGACGACTGGTTACTTATAGCTCTTGCTGCCCTCG GCGCGCGCGCGACGGCGGCGGCGGCGGCGGCGGCGACTGGTTACTTATAGCTCTTGCTGCCCTCG T C CHD1 Ensembl:ENSG00000153922 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr5:98928606..98928922;chr5:98928706..98928957 26863196,26863410 MeRIP-seq:(Medium) rs796077946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3782790,Human_RBP_ID_4846540,Human_RBP_ID_8136897,Human_RBP_ID_8943890,Human_RBP_ID_9335267,Human_RBP_ID_18501740 65590 RMVar_ID_65590 Human_SNP_ID_242818452 m1A Human chr5 - 98928849 98928849 98928849 CGTCATGGCGGCTGCCGGGGGCAGATAAGCGGAGGGAGCGGGAGCGCGCGCGCGACGGCGGCGGC CGTCATGGCGGCTGCCGGGGGCAGATAAGCGGCGGGAGCGGGAGCGCGCGCGCGACGGCGGCGGC T G CHD1 Ensembl:ENSG00000153922 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:98928678..98928992 26863196 MeRIP-seq:(Medium) rs1260947356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3782790,Human_RBP_ID_4845859,Human_RBP_ID_5151112,Human_RBP_ID_8136897,Human_RBP_ID_9335267,Human_RBP_ID_18501740 65591 RMVar_ID_65591 Human_SNP_ID_242829265 m1A Human chr5 - 98973319 98973319 98973319 CCTACCACTTCTCCTCCTTCTTCCTTCTCCTCATTCTTCTTTTCTTCTTCCTTCTCCTTCTTCTT CCTACCACTTCTCCTCCTTCTTCCTTCTCCTCCTTCTTCTTTTCTTCTTCCTTCTCCTTCTTCTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:98973240..98973412 26863196 MeRIP-seq:(Medium) rs1200946825 Functional Loss SNV dbSNP153 33..33 33 - - - 65592 RMVar_ID_65592 Human_SNP_ID_243227326 m1A Human chr5 - 100535937 100535937 100535937 CTCACCTGACCGTCCTGACCACGAAGTACACCAGCACCGCGCCGCTCACCACCATCAACACGGTC CTCACCTGACCGTCCTGACCACGAAGTACACCGGCACCGCGCCGCTCACCACCATCAACACGGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:100535743..100535939 32194978 MeRIP-seq:(Medium) rs776960906 Functional Loss SNV dbSNP153 33..33 33 - - - 65593 RMVar_ID_65593 Human_SNP_ID_243233904 m1A Human chr5 - 100561986 100561986 100561986 TTAATATGGCATAGTTTATATTTATTTATAAAATAAATTATTATTCTGTTTCTGACATAGCAAAC TTAATATGGCATAGTTTATATTTATTTATAAACTAAATTATTATTCTGTTTCTGACATAGCAAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:100561984..100562068 26863196 MeRIP-seq:(Medium) rs1399981910 Functional Loss SNV dbSNP153 33..33 33 - - - 65594 RMVar_ID_65594 Human_SNP_ID_243791654 m1A Human chr5 - 102755184 102755171 102755184 GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCCAGCCGGGTCCGCCGCTCGCCCTCGACTCCTGGG GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCC_____________GCTCGCCCTCGACTCCTGGG CGGCGGACCCGGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:102755141..102755277 26863196 MeRIP-seq:(Medium) rs1234553285 Functional Loss DEL dbSNP153 33..45 33 - - - 65595 RMVar_ID_65595 Human_SNP_ID_243791661 m1A Human chr5 - 102755184 102755183 102755184 GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCCAGCCGGGTCCGCCGCTCGCCCTCGACTCCTGGG GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCC_GCCGGGTCCGCCGCTCGCCCTCGACTCCTGGG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:102755141..102755277 26863196 MeRIP-seq:(Medium) rs1391505792 Functional Loss DEL dbSNP153 33..33 33 - - - 65596 RMVar_ID_65596 Human_SNP_ID_243791662 m1A Human chr5 - 102755184 102755184 102755184 GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCCAGCCGGGTCCGCCGCTCGCCCTCGACTCCTGGG GGGGCTCCCTCTCCTCGGCGTGCGCCGGGCCCGGCCGGGTCCGCCGCTCGCCCTCGACTCCTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:102755141..102755277 26863196 MeRIP-seq:(Medium) rs1165504234 Functional Loss SNV dbSNP153 33..33 33 - - - 65597 RMVar_ID_65597 Human_SNP_ID_243791698 m1A Human chr5 - 102755229 102755223 102755229 CCTGGGCGGGGACAGGCTGAGCACGCGGAGGCAGCGGCGGTGGCGGGGGCTCCCTCTCCTCGGCG CCTGGGCGGGGACAGGCTGAGCACGCGGAGGC______GGTGGCGGGGGCTCCCTCTCCTCGGCG CGCCGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:102755182..102755254 26863196 MeRIP-seq:(Medium) rs1315232968 Functional Loss DEL dbSNP153 33..38 33 - - - 65598 RMVar_ID_65598 Human_SNP_ID_243791709 m1A Human chr5 - 102755250 102755250 102755250 GTTAGTTGGAGGCTCCGGCTCCCTGGGCGGGGACAGGCTGAGCACGCGGAGGCAGCGGCGGTGGC GTTAGTTGGAGGCTCCGGCTCCCTGGGCGGGGGCAGGCTGAGCACGCGGAGGCAGCGGCGGTGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:102755140..102755249 26863196 MeRIP-seq:(Medium) rs1324002257 Functional Loss SNV dbSNP153 33..33 33 - - - 65599 RMVar_ID_65599 Human_SNP_ID_243816740 m1A Human chr5 + 102866262 102866262 102866262 TTGTTTTTCCAAGCAGCTGTTTGGCTTTCCGAAGCCCACTTTCTGTCTTTAAGAGGTGGGTGTTC TTGTTTTTCCAAGCAGCTGTTTGGCTTTCCGAGGCCCACTTTCTGTCTTTAAGAGGTGGGTGTTC A G PAM Ensembl:ENSG00000145730 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:102866011..102866262 32194978 MeRIP-seq:(Medium) rs747290879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846549 Human_Splice_Rec_677957,Human_Splice_Rec_677961,Human_Splice_Rec_677967,Human_Splice_Rec_677969,Human_Splice_Rec_678015,Human_Splice_Rec_678059,Human_Splice_Rec_678063,Human_Splice_Rec_678107,Human_Splice_Rec_678151,Human_Splice_Rec_678197 RMVar_hsa_circ_26768,RMVar_hsa_circ_291554,RMVar_hsa_circ_310271,RMVar_hsa_circ_111807,RMVar_hsa_circ_19162,RMVar_hsa_circ_23488,RMVar_hsa_circ_233500,RMVar_hsa_circ_233501 65600 RMVar_ID_65600 Human_SNP_ID_243816949 m1A Human chr5 + 102867253 102867253 102867253 GAGTTTAGATTCCATTATGTTCAAGAATATTGAAATTGCCCTCTTTTTTAAGGTTTAAAGAAACT GAGTTTAGATTCCATTATGTTCAAGAATATTGTAATTGCCCTCTTTTTTAAGGTTTAAAGAAACT A T PAM Ensembl:ENSG00000145730 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:102867251..102867300 32194978 MeRIP-seq:(Medium) rs1166463963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26768,RMVar_hsa_circ_291554,RMVar_hsa_circ_310271,RMVar_hsa_circ_111807,RMVar_hsa_circ_19162,RMVar_hsa_circ_23488,RMVar_hsa_circ_233500,RMVar_hsa_circ_233501 65601 RMVar_ID_65601 Human_SNP_ID_243848754 m1A Human chr5 - 103009802 103009802 103009802 CCCCATTGGAAAAGTTCATCACAAATCCTTGTACAGGTTCTTGGTCCCCAAAATGAGGCTTCCCA CCCCATTGGAAAAGTTCATCACAAATCCTTGTGCAGGTTCTTGGTCCCCAAAATGAGGCTTCCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:103006917..103009802 32194978 MeRIP-seq:(Medium) rs762543056 Functional Loss SNV dbSNP153 33..33 33 - - - 65602 RMVar_ID_65602 Human_SNP_ID_243876295 m1A Human chr5 + 103120413 103120413 103120413 CTCTTGACAAACACCTCACCCCTGCCTCCGGGATGAAAGGGGGTAACCTAGACCTGAATGGGCTT CTCTTGACAAACACCTCACCCCTGCCTCCGGGTTGAAAGGGGGTAACCTAGACCTGAATGGGCTT A T PPIP5K2 Ensembl:ENSG00000145725 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:103120362..103120469 26863196 MeRIP-seq:(Medium) rs781892962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845860,Human_RBP_ID_5477047,Human_RBP_ID_8894057,Human_RBP_ID_9307024 Human_Splice_Rec_678395,Human_Splice_Rec_678451,Human_Splice_Rec_678473,Human_Splice_Rec_678479,Human_Splice_Rec_678537 Human_miRNA_ID_2582097,Human_miRNA_ID_2660069 RMVar_hsa_circ_116387,RMVar_hsa_circ_233518 65603 RMVar_ID_65603 Human_SNP_ID_243908985 m1A Human chr5 - 103258789 103258789 103258789 ACTGCGGCGCCGAGATCCAGGCAGAGGCCGCCAGCCGAGCCAGCCGGGTACCCTCTCCTCTCCCA ACTGCGGCGCCGAGATCCAGGCAGAGGCCGCCGGCCGAGCCAGCCGGGTACCCTCTCCTCTCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:103258745..103258927 26863196 MeRIP-seq:(Medium) rs966895405 Functional Loss SNV dbSNP153 33..33 33 - - - 65604 RMVar_ID_65604 Human_SNP_ID_243908986 m1A Human chr5 - 103258789 103258789 103258789 ACTGCGGCGCCGAGATCCAGGCAGAGGCCGCCAGCCGAGCCAGCCGGGTACCCTCTCCTCTCCCA ACTGCGGCGCCGAGATCCAGGCAGAGGCCGCCCGCCGAGCCAGCCGGGTACCCTCTCCTCTCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:103258745..103258927 26863196 MeRIP-seq:(Medium) rs966895405 Functional Loss SNV dbSNP153 33..33 33 - - - 65605 RMVar_ID_65605 Human_SNP_ID_243910986 m1A Human chr5 + 103265840 103265840 103265840 CTCCTGCTAGTTTTATTCTCTTTTGCAGTTAGAATTGATATCATGTTATAAGTTGTGTTACTTGT CTCCTGCTAGTTTTATTCTCTTTTGCAGTTAGTATTGATATCATGTTATAAGTTGTGTTACTTGT A T MACIR Ensembl:ENSG00000181751 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:103265839..103265926 26863196 MeRIP-seq:(Medium) rs371635634 Functional Loss SNV dbSNP153 33..33 33 - - - 65606 RMVar_ID_65606 Human_SNP_ID_243981972 m1A Human chr5 - 103549137 103549137 103549137 TTTAATACTTGCAGATTCTAAGATTACATTGTAAAATTCCAGGTTTTCATAATGTTAAAATAGGA TTTAATACTTGCAGATTCTAAGATTACATTGTGAAATTCCAGGTTTTCATAATGTTAAAATAGGA T C NUDT12 Ensembl:ENSG00000112874 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10057864 Functional Loss SNV dbSNP153 33..33 33 - - - 65607 RMVar_ID_65607 Human_SNP_ID_243981990 m1A Human chr5 - 103549232 103549232 103549232 AATAAAATTCGAGCTACATAAGTATATGGAAAATAATGTACCTTGATTATTATGAAATAGAGCAT AATAAAATTCGAGCTACATAAGTATATGGAAAGTAATGTACCTTGATTATTATGAAATAGAGCAT T C NUDT12 Ensembl:ENSG00000112874 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10057908 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7913,GWAS_ID_7914,GWAS_ID_7915,GWAS_ID_7916,GWAS_ID_7917 65608 RMVar_ID_65608 Human_SNP_ID_243981991 m1A Human chr5 - 103549232 103549232 103549232 AATAAAATTCGAGCTACATAAGTATATGGAAAATAATGTACCTTGATTATTATGAAATAGAGCAT AATAAAATTCGAGCTACATAAGTATATGGAAACTAATGTACCTTGATTATTATGAAATAGAGCAT T G NUDT12 Ensembl:ENSG00000112874 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10057908 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7913,GWAS_ID_7914,GWAS_ID_7915,GWAS_ID_7916,GWAS_ID_7917 65609 RMVar_ID_65609 Human_SNP_ID_29889004 m1A Human chr1 + 120001276 120001276 120001276 GTACCAAGAGTGGGGTTTTTGCCAGAGTGCCAACTATCCCGAGGGAAACTTTGGAGGGAACCAGC GTACCAAGAGTGGGGTTTTTGCCAGAGTGCCAGCTATCCCGAGGGAAACTTTGGAGGGAACCAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:120001274..120001400 26863196 MeRIP-seq:(Medium) rs3103927 Functional Loss SNV dbSNP153 33..33 33 - - - 65610 RMVar_ID_65610 Human_SNP_ID_29896802 m1A Human chr1 - 120029989 120029989 120029989 CTTACTTCTAATGTGCATTTGTTTTTATTTTTAGCATTGCAGTGTCGAGATGGCTATGAACCCTG CTTACTTCTAATGTGCATTTGTTTTTATTTTTGGCATTGCAGTGTCGAGATGGCTATGAACCCTG T C NOTCH2 Ensembl:ENSG00000134250 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:120029967..120030043;chr1:120029971..120030058 26863196 MeRIP-seq:(Medium) rs1553210735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_115713,Human_Splice_Rec_115829,Human_Splice_Rec_115859,Human_Splice_Rec_115867,Human_Splice_Rec_115875,Human_Splice_Rec_115879,Human_Splice_Rec_115885 RMVar_hsa_circ_341993,RMVar_hsa_circ_298274 65611 RMVar_ID_65611 Human_SNP_ID_29907296 m1A Human chr1 - 120069423 120069422 120069423 ATCTGCCCAGGCGGCGGCGGCGGCGGCGGAGGAGGAGGCGACCGAGAAGATGCCCGCCCTGCGCC ATCTGCCCAGGCGGCGGCGGCGGCGGCGGAGG_GGAGGCGACCGAGAAGATGCCCGCCCTGCGCC CT C NOTCH2 Ensembl:ENSG00000134250 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:120069332..120069597 26863196 MeRIP-seq:(Medium) rs782563113 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_20026,Human_RBP_ID_97060,Human_RBP_ID_221961,Human_RBP_ID_4072993 Human_Splice_Rec_115711,Human_Splice_Rec_115781,Human_Splice_Rec_115865,Human_Splice_Rec_115881,Human_Splice_Rec_115887 65612 RMVar_ID_65612 Human_SNP_ID_29907298 m1A Human chr1 - 120069423 120069423 120069423 ATCTGCCCAGGCGGCGGCGGCGGCGGCGGAGGAGGAGGCGACCGAGAAGATGCCCGCCCTGCGCC ATCTGCCCAGGCGGCGGCGGCGGCGGCGGAGGCGGAGGCGACCGAGAAGATGCCCGCCCTGCGCC T G NOTCH2 Ensembl:ENSG00000134250 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:120069332..120069597 26863196 MeRIP-seq:(Medium) rs782183187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20026,Human_RBP_ID_97060,Human_RBP_ID_221961,Human_RBP_ID_4072993 Human_Splice_Rec_115711,Human_Splice_Rec_115781,Human_Splice_Rec_115865,Human_Splice_Rec_115881,Human_Splice_Rec_115887 65613 RMVar_ID_65613 Human_SNP_ID_29907301 m1A Human chr1 - 120069426 120069426 120069426 TGGATCTGCCCAGGCGGCGGCGGCGGCGGCGGAGGAGGAGGCGACCGAGAAGATGCCCGCCCTGC TGGATCTGCCCAGGCGGCGGCGGCGGCGGCGGCGGAGGAGGCGACCGAGAAGATGCCCGCCCTGC T G NOTCH2 Ensembl:ENSG00000134250 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:120069311..120069659;chr1:120069397..120069462;chr1:120069401..120069668;chr1:120069387..120069661 26863196 MeRIP-seq:(Medium) rs3010135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20026,Human_RBP_ID_97060,Human_RBP_ID_221961,Human_RBP_ID_804580,Human_RBP_ID_4072993 Human_Splice_Rec_115711,Human_Splice_Rec_115781,Human_Splice_Rec_115865,Human_Splice_Rec_115881,Human_Splice_Rec_115887 65614 RMVar_ID_65614 Human_SNP_ID_29907414 m1A Human chr1 + 120069545 120069545 120069545 TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGCAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:120069399..120069625 26863196 MeRIP-seq:(Medium) rs587606395 Functional Loss SNV dbSNP153 33..33 33 - - - 65615 RMVar_ID_65615 Human_SNP_ID_29907415 m1A Human chr1 + 120069545 120069545 120069545 TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGGAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:120069399..120069625 26863196 MeRIP-seq:(Medium) rs587606395 Functional Loss SNV dbSNP153 33..33 33 - - - 65616 RMVar_ID_65616 Human_SNP_ID_29956146 m1A Human chr1 - 120341817 120341817 120341817 GGTGGGGTGGAAATAGCGGCTGCTTCTTTTCCAAGGACTTATTTAATGGGGATGTGTTCAAGGCA GGTGGGGTGGAAATAGCGGCTGCTTCTTTTCCGAGGACTTATTTAATGGGGATGTGTTCAAGGCA T C AC244669.1 Ensembl:ENSG00000223804 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:120341774..120341871;chr1:120341763..120341850 26863196 MeRIP-seq:(Medium) rs1553236244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3178643,Human_miRNA_ID_3194103 65617 RMVar_ID_65617 Human_SNP_ID_29956218 m1A Human chr1 - 120342009 120342009 120342009 TGGAATCCAGCAGCGGCGAGCAGCAGCTGGGCAGTCACATCTGGAAATGGAAAGCCGACCTCCAC TGGAATCCAGCAGCGGCGAGCAGCAGCTGGGCGGTCACATCTGGAAATGGAAAGCCGACCTCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:120341962..120342037 26863196 MeRIP-seq:(Medium) rs3009830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4077501 65618 RMVar_ID_65618 Human_SNP_ID_29959864 m1A Human chr1 - 120355053 120355053 120355053 AAGTAACAGGAGTCAGTCAGCACATACTGAGTACAATGGAAAAACCGCCCCCGAAAAACACCAAC AAGTAACAGGAGTCAGTCAGCACATACTGAGTGCAATGGAAAAACCGCCCCCGAAAAACACCAAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:120355016..120355087;chr1:120355003..120355136 26863196 MeRIP-seq:(Medium) rs1376685764 Functional Loss SNV dbSNP153 33..33 33 - - - 65619 RMVar_ID_65619 Human_SNP_ID_29959880 m1A Human chr1 - 120355081 120355081 120355081 AATTACAGTCCAGTTTCCCCACATGTGGAAGTAACAGGAGTCAGTCAGCACATACTGAGTACAAT AATTACAGTCCAGTTTCCCCACATGTGGAAGTGACAGGAGTCAGTCAGCACATACTGAGTACAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:120355032..120355099 26863196 MeRIP-seq:(Medium) rs1553237975 Functional Loss SNV dbSNP153 33..33 33 - - - 65620 RMVar_ID_65620 Human_SNP_ID_29976480 m1A Human chr1 + 120415216 120415216 120415216 TGTGGCGCCAGGAGCGGGCCGAGGCGCGGCGCACGGATGCCATCTGGATGGGAAGTTACGGTTTA TGTGGCGCCAGGAGCGGGCCGAGGCGCGGCGCGCGGATGCCATCTGGATGGGAAGTTACGGTTTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:120415169..120415288 26863196 MeRIP-seq:(Medium) rs61806646 Functional Loss SNV dbSNP153 33..33 33 - - - 65621 RMVar_ID_65621 Human_SNP_ID_29986979 m1A Human chr1 + 120461301 120461301 120461301 GCTGGATGAGAAAGGGCCTGAAGTCTTGCAGGACTCACTGGATAGATGTTATTCAACTCCTTCAG GCTGGATGAGAAAGGGCCTGAAGTCTTGCAGGGCTCACTGGATAGATGTTATTCAACTCCTTCAG A G NBPF8 Ensembl:ENSG00000270231 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:120461276..120461300 32194978 MeRIP-seq:(Medium) rs1221770379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_115968,Human_Splice_Rec_116012 65622 RMVar_ID_65622 Human_SNP_ID_29986980 m1A Human chr1 + 120461301 120461301 120461301 GCTGGATGAGAAAGGGCCTGAAGTCTTGCAGGACTCACTGGATAGATGTTATTCAACTCCTTCAG GCTGGATGAGAAAGGGCCTGAAGTCTTGCAGGTCTCACTGGATAGATGTTATTCAACTCCTTCAG A T NBPF8 Ensembl:ENSG00000270231 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:120461276..120461300 32194978 MeRIP-seq:(Medium) rs1221770379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_115968,Human_Splice_Rec_116012 65623 RMVar_ID_65623 Human_SNP_ID_30027855 m1A Human chr1 - 120724200 120724200 120724200 AGCACAGCCAGAGCGCCAGCAGCGCCCACAGCAGAGCGGGACGCAGGGCGGGCATCTTCTCGGTC AGCACAGCCAGAGCGCCAGCAGCGCCCACAGCGGAGCGGGACGCAGGGCGGGCATCTTCTCGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:120724105..120724242 26863196 MeRIP-seq:(Medium) rs1255465000 Functional Loss SNV dbSNP153 33..33 33 - - - 65624 RMVar_ID_65624 Human_SNP_ID_30071760 m1A Human chr1 - 120942331 120942331 120942331 CTCTCCGTGATGTCACCGACAACGCCTTCTGGATCCCCGTCTGCTCTTCCGCCTCACCCAACGCC CTCTCCGTGATGTCACCGACAACGCCTTCTGGTTCCCCGTCTGCTCTTCCGCCTCACCCAACGCC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:120942212..120942341 26863196 MeRIP-seq:(Medium) rs1418761088 Functional Loss SNV dbSNP153 33..33 33 - - - 65625 RMVar_ID_65625 Human_SNP_ID_30093287 m1A Human chr1 - 121016860 121016860 121016860 TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAATTCCCGGTCAAGATAAGAGGTATTTTTGCTCT TTCTCGCCTCCCACGCGGGAGACCCGGGTTCAGTTCCCGGTCAAGATAAGAGGTATTTTTGCTCT T C AC241377.3 Ensembl:ENSG00000275585 Pseudogene intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1288766400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1410977,Human_RBP_ID_3990822,Human_RBP_ID_5272897,Human_RBP_ID_5685118,Human_RBP_ID_8241611,Human_RBP_ID_8284301,Human_RBP_ID_17724541,Human_RBP_ID_18204499,Human_RBP_ID_22126889,Human_RBP_ID_22779727,Human_RBP_ID_23112449,Human_RBP_ID_26367620,Human_RBP_ID_27167278 65626 RMVar_ID_65626 Human_SNP_ID_30137815 m1A Human chr1 - 121183615 121183615 121183615 GAAAACAGAAAAAAAAAACTAATTTCCTTCCCAATATTAGGACTTAGAAAAGCTCTAGGTCCCGC GAAAACAGAAAAAAAAAACTAATTTCCTTCCCTATATTAGGACTTAGAAAAGCTCTAGGTCCCGC T A FAM72B Ensembl:ENSG00000188610 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:121183565..121183649 26863196 MeRIP-seq:(Medium) rs587606817 Functional Loss SNV dbSNP153 33..33 33 - - - 65627 RMVar_ID_65627 Human_SNP_ID_30137816 m1A Human chr1 - 121183615 121183615 121183615 GAAAACAGAAAAAAAAAACTAATTTCCTTCCCAATATTAGGACTTAGAAAAGCTCTAGGTCCCGC GAAAACAGAAAAAAAAAACTAATTTCCTTCCCGATATTAGGACTTAGAAAAGCTCTAGGTCCCGC T C FAM72B Ensembl:ENSG00000188610 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:121183565..121183649 26863196 MeRIP-seq:(Medium) rs587606817 Functional Loss SNV dbSNP153 33..33 33 - - - 65628 RMVar_ID_65628 Human_SNP_ID_30137970 m1A Human chr1 - 121184136 121184136 121184136 TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCAAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCTAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG T A FAM72B Ensembl:ENSG00000188610 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:121183915..121184200;chr1:121183907..121184200;chr1:121183930..121184200 26863196 MeRIP-seq:(Medium) rs1172651974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_116697 65629 RMVar_ID_65629 Human_SNP_ID_30137971 m1A Human chr1 - 121184136 121184136 121184136 TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCAAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCGAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG T C FAM72B Ensembl:ENSG00000188610 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:121183915..121184200;chr1:121183907..121184200;chr1:121183930..121184200 26863196 MeRIP-seq:(Medium) rs1172651974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_116697 65630 RMVar_ID_65630 Human_SNP_ID_30138322 m1A Human chr1 + 121185091 121185091 121185091 AGAGGGGAGGAGAGCTCTGAGTGGGAAGCGGAACCGGGGGCCTGGGACCCGTCGCGTCAGAGCCA AGAGGGGAGGAGAGCTCTGAGTGGGAAGCGGAGCCGGGGGCCTGGGACCCGTCGCGTCAGAGCCA A G SRGAP2C Ensembl:ENSG00000171943 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:121184992..121185137;chr1:121184990..121185139;chr1:121184986..121185150;chr1:121184983..121185152 26863196 MeRIP-seq:(Medium) rs28594517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26311686,Human_RBP_ID_27798440 Human_Splice_Rec_116705 65631 RMVar_ID_65631 Human_SNP_ID_30182707 m1A Human chr1 + 121374827 121374827 121374827 AGGTAAAAGTGAACTTCTGTTTCCTTTTCAGCACCAAGCCAAGTACACGGAGAATAAGCTGAAGG AGGTAAAAGTGAACTTCTGTTTCCTTTTCAGCGCCAAGCCAAGTACACGGAGAATAAGCTGAAGG A G SRGAP2C Ensembl:ENSG00000171943 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61806690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18158548,Human_RBP_ID_18523707,Human_RBP_ID_27800681 Human_Splice_Rec_116716,Human_Splice_Rec_116730 Human_miRNA_ID_1861242,Human_miRNA_ID_2464533,Human_miRNA_ID_2464534 RMVar_hsa_circ_297478,RMVar_hsa_circ_308833,RMVar_hsa_circ_9042,RMVar_hsa_circ_287284,RMVar_hsa_circ_135771 65632 RMVar_ID_65632 Human_SNP_ID_30192455 m1A Human chr1 - 121401086 121401086 121401086 CGTTTCATTTCCTCATTTCATCATTTCATTTCATCCTTTCATCATTTCATCTCATCATCTCATCC CGTTTCATTTCCTCATTTCATCATTTCATTTCTTCCTTTCATCATTTCATCTCATCATCTCATCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:121400902..121401134 26863196 MeRIP-seq:(Medium) rs1258493318 Functional Loss SNV dbSNP153 33..33 33 - - - 65633 RMVar_ID_65633 Human_SNP_ID_30223742 m1A Human chr1 + 121519533 121519518 121519534 GCGCGAGGCTCGGGTCCCCGCGGGCAGAGGGCATCGCTGGCGCTCCGGGCAGGGTTGGCGGGGAG GCGCGAGGCTCGGGTCCC________________CGCTGGCGCTCCGGGCAGGGTTGGCGGGGAG CCGCGGGCAGAGGGCAT C EMBP1 Ensembl:ENSG00000231752 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:121519483..121519555 26863196 MeRIP-seq:(Medium) rs1553377125 Functional Loss DEL dbSNP153 19..34 33 - - - 65634 RMVar_ID_65634 Human_SNP_ID_30223749 m1A Human chr1 + 121519533 121519533 121519533 GCGCGAGGCTCGGGTCCCCGCGGGCAGAGGGCATCGCTGGCGCTCCGGGCAGGGTTGGCGGGGAG GCGCGAGGCTCGGGTCCCCGCGGGCAGAGGGCTTCGCTGGCGCTCCGGGCAGGGTTGGCGGGGAG A T EMBP1 Ensembl:ENSG00000231752 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:121519483..121519555 26863196 MeRIP-seq:(Medium) rs1306642770 Functional Loss SNV dbSNP153 33..33 33 - - - 65635 RMVar_ID_65635 Human_SNP_ID_402646953 m1A Human chr9 - 75028091 75028091 75028091 CCGCGGCGGTTTCGGCGGCAGCGGCGGCGGCCACGCGCAGCACCGAGGAGGAGGAGGAGAGGCTT CCGCGGCGGTTTCGGCGGCAGCGGCGGCGGCCTCGCGCAGCACCGAGGAGGAGGAGGAGAGGCTT T A CARNMT1 Ensembl:ENSG00000156017 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:75028050..75028384 26863196 MeRIP-seq:(Medium) rs200378073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256761,Human_RBP_ID_720406,Human_RBP_ID_5035720,Human_RBP_ID_22118722 Human_Splice_Rec_1053279,Human_Splice_Rec_1053301 65636 RMVar_ID_65636 Human_SNP_ID_402646954 m1A Human chr9 - 75028091 75028091 75028091 CCGCGGCGGTTTCGGCGGCAGCGGCGGCGGCCACGCGCAGCACCGAGGAGGAGGAGGAGAGGCTT CCGCGGCGGTTTCGGCGGCAGCGGCGGCGGCCGCGCGCAGCACCGAGGAGGAGGAGGAGAGGCTT T C CARNMT1 Ensembl:ENSG00000156017 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:75028050..75028384 26863196 MeRIP-seq:(Medium) rs200378073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256761,Human_RBP_ID_720406,Human_RBP_ID_5035720,Human_RBP_ID_22118722 Human_Splice_Rec_1053279,Human_Splice_Rec_1053301 65637 RMVar_ID_65637 Human_SNP_ID_402647050 m1A Human chr9 - 75028271 75028271 75028271 CCGCCACCACGCTGTCGGTCGCGGAGAGACGCAAGCGAGCCAGGCCGAGGGCCGCGGCGGCGATG CCGCCACCACGCTGTCGGTCGCGGAGAGACGCGAGCGAGCCAGGCCGAGGGCCGCGGCGGCGATG T C CARNMT1 Ensembl:ENSG00000156017 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:75027064..75028423 26863196 MeRIP-seq:(Medium) rs910541986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256762,Human_RBP_ID_720407,Human_RBP_ID_5031301,Human_RBP_ID_9408105 65638 RMVar_ID_65638 Human_SNP_ID_402661644 m1A Human chr9 - 75088098 75088098 75088098 GCGTGGGGAAAGGGGCTGTGGGCCTCTCGGGGAGCGAGCTGCGGGTAGCGGCGCACTGGGTACAG GCGTGGGGAAAGGGGCTGTGGGCCTCTCGGGGTGCGAGCTGCGGGTAGCGGCGCACTGGGTACAG T A NMRK1 Ensembl:ENSG00000106733 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:75087788..75088185 26863196 MeRIP-seq:(Medium) rs928531531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1053305,Human_Splice_Rec_1053323,Human_Splice_Rec_1053341,Human_Splice_Rec_1053355,Human_Splice_Rec_1053369 65639 RMVar_ID_65639 Human_SNP_ID_402661900 m1A Human chr9 + 75088579 75088579 75088579 TCCCGCAGCCAAGGGTGGGCGCCGGTCCTAGGAGGCGCACGGTTGTAAGCCAGACAAAAAGAACT TCCCGCAGCCAAGGGTGGGCGCCGGTCCTAGGGGGCGCACGGTTGTAAGCCAGACAAAAAGAACT A G OSTF1 Ensembl:ENSG00000134996 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:75088528..75117515;chr9:75088531..75088763 26863196 MeRIP-seq:(Medium) rs921725499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036201,Human_RBP_ID_18427157,Human_RBP_ID_24306941 65640 RMVar_ID_65640 Human_SNP_ID_402861882 m1A Human chr9 + 75890881 75890881 75890881 CGGGAGCCAAGCCGGGCGAAACCCAACTGCGGAGGACGCCCGCCCCACTCAGCCTCCTCCTGCGT CGGGAGCCAAGCCGGGCGAAACCCAACTGCGGTGGACGCCCGCCCCACTCAGCCTCCTCCTGCGT A T PCSK5 Ensembl:ENSG00000099139 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:75890831..75890918 26863196 MeRIP-seq:(Medium) rs1446629241 Functional Loss SNV dbSNP153 33..33 33 - - - 65641 RMVar_ID_65641 Human_SNP_ID_403027049 m1A Human chr9 + 76571874 76571874 76571874 GCCCTTCCTCCTGGGAAACGGGGTGCGGCCGGAAAGGCGGCCGCCCCCTCGCCCGTCACGCAACG GCCCTTCCTCCTGGGAAACGGGGTGCGGCCGGGAAGGCGGCCGCCCCCTCGCCCGTCACGCAACG A G GCNT1 Ensembl:ENSG00000187210 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr9:76571817..76571938;chr9:76571803..76571963 26863196 MeRIP-seq:(Medium) rs1374463254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271187,Human_RBP_ID_723042,Human_RBP_ID_1118816,Human_RBP_ID_1227666,Human_RBP_ID_1247954,Human_RBP_ID_1340087,Human_RBP_ID_1403999,Human_RBP_ID_1708359,Human_RBP_ID_2065422,Human_RBP_ID_3220835,Human_RBP_ID_3902203,Human_RBP_ID_5031489,Human_RBP_ID_5226385,Human_RBP_ID_5277634,Human_RBP_ID_5431311,Human_RBP_ID_5454644,Human_RBP_ID_5482222,Human_RBP_ID_5516317,Human_RBP_ID_5634208,Human_RBP_ID_7934901,Human_RBP_ID_8161164,Human_RBP_ID_8276331,Human_RBP_ID_8706244,Human_RBP_ID_8929115,Human_RBP_ID_9237427,Human_RBP_ID_10442672,Human_RBP_ID_16699058,Human_RBP_ID_17056757,Human_RBP_ID_17065667,Human_RBP_ID_17070622,Human_RBP_ID_17174885,Human_RBP_ID_17202135,Human_RBP_ID_17322435,Human_RBP_ID_17436644,Human_RBP_ID_17550143,Human_RBP_ID_17716762,Human_RBP_ID_18137601,Human_RBP_ID_18185737,Human_RBP_ID_18203426,Human_RBP_ID_18212308,Human_RBP_ID_18453651,Human_RBP_ID_18521240,Human_RBP_ID_18542468,Human_RBP_ID_18909983,Human_RBP_ID_21659949,Human_RBP_ID_21955681,Human_RBP_ID_22118262,Human_RBP_ID_22341121,Human_RBP_ID_22411733,Human_RBP_ID_22838776,Human_RBP_ID_23095372,Human_RBP_ID_23141717,Human_RBP_ID_23201447,Human_RBP_ID_23300332,Human_RBP_ID_23316765,Human_RBP_ID_24307134,Human_RBP_ID_24442917,Human_RBP_ID_24523939,Human_RBP_ID_24537439,Human_RBP_ID_26228359,Human_RBP_ID_26564268,Human_RBP_ID_26739101,Human_RBP_ID_26752322,Human_RBP_ID_27137772,Human_RBP_ID_27162520,Human_RBP_ID_27376066,Human_RBP_ID_27547904,Human_RBP_ID_27570705,Human_RBP_ID_27786674 RMVar_hsa_circ_257216 65642 RMVar_ID_65642 Human_SNP_ID_403027050 m1A Human chr9 + 76571875 76571875 76571875 CCCTTCCTCCTGGGAAACGGGGTGCGGCCGGAAAGGCGGCCGCCCCCTCGCCCGTCACGCAACGC CCCTTCCTCCTGGGAAACGGGGTGCGGCCGGAGAGGCGGCCGCCCCCTCGCCCGTCACGCAACGC A G GCNT1 Ensembl:ENSG00000187210 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:76571826..76571900 26863196 MeRIP-seq:(Medium) rs1300426441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271187,Human_RBP_ID_720549,Human_RBP_ID_1118816,Human_RBP_ID_1227666,Human_RBP_ID_1247954,Human_RBP_ID_1340087,Human_RBP_ID_1403999,Human_RBP_ID_1708359,Human_RBP_ID_2065422,Human_RBP_ID_3220835,Human_RBP_ID_3902203,Human_RBP_ID_5031489,Human_RBP_ID_5226385,Human_RBP_ID_5277634,Human_RBP_ID_5431311,Human_RBP_ID_5454644,Human_RBP_ID_5482222,Human_RBP_ID_5516317,Human_RBP_ID_5634208,Human_RBP_ID_7934901,Human_RBP_ID_8161164,Human_RBP_ID_8276331,Human_RBP_ID_8706244,Human_RBP_ID_8929115,Human_RBP_ID_9237427,Human_RBP_ID_10442672,Human_RBP_ID_16699058,Human_RBP_ID_17056757,Human_RBP_ID_17065667,Human_RBP_ID_17070622,Human_RBP_ID_17174885,Human_RBP_ID_17202135,Human_RBP_ID_17322435,Human_RBP_ID_17436644,Human_RBP_ID_17550143,Human_RBP_ID_17716762,Human_RBP_ID_18137601,Human_RBP_ID_18185737,Human_RBP_ID_18203426,Human_RBP_ID_18212308,Human_RBP_ID_18453651,Human_RBP_ID_18521240,Human_RBP_ID_18542468,Human_RBP_ID_18909983,Human_RBP_ID_21659949,Human_RBP_ID_21955681,Human_RBP_ID_22118262,Human_RBP_ID_22341121,Human_RBP_ID_22411733,Human_RBP_ID_22838776,Human_RBP_ID_23095372,Human_RBP_ID_23141717,Human_RBP_ID_23201447,Human_RBP_ID_23300332,Human_RBP_ID_23316765,Human_RBP_ID_24307134,Human_RBP_ID_24442917,Human_RBP_ID_24523939,Human_RBP_ID_24537439,Human_RBP_ID_26243748,Human_RBP_ID_26564268,Human_RBP_ID_26739101,Human_RBP_ID_26752322,Human_RBP_ID_27137772,Human_RBP_ID_27162520,Human_RBP_ID_27376066,Human_RBP_ID_27547904,Human_RBP_ID_27570800,Human_RBP_ID_27786674 RMVar_hsa_circ_257216 65643 RMVar_ID_65643 Human_SNP_ID_403027051 m1A Human chr9 + 76571876 76571876 76571876 CCTTCCTCCTGGGAAACGGGGTGCGGCCGGAAAGGCGGCCGCCCCCTCGCCCGTCACGCAACGCA CCTTCCTCCTGGGAAACGGGGTGCGGCCGGAAGGGCGGCCGCCCCCTCGCCCGTCACGCAACGCA A G GCNT1 Ensembl:ENSG00000187210 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:76571826..76571900 26863196 MeRIP-seq:(Medium) rs879180661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271187,Human_RBP_ID_720549,Human_RBP_ID_1118816,Human_RBP_ID_1227666,Human_RBP_ID_1247954,Human_RBP_ID_1340087,Human_RBP_ID_1403999,Human_RBP_ID_1705901,Human_RBP_ID_2065422,Human_RBP_ID_3220835,Human_RBP_ID_3902203,Human_RBP_ID_5031489,Human_RBP_ID_5226385,Human_RBP_ID_5277634,Human_RBP_ID_5431311,Human_RBP_ID_5454644,Human_RBP_ID_5482222,Human_RBP_ID_5516317,Human_RBP_ID_5634208,Human_RBP_ID_7934901,Human_RBP_ID_8161164,Human_RBP_ID_8276331,Human_RBP_ID_8706244,Human_RBP_ID_8929115,Human_RBP_ID_9237427,Human_RBP_ID_10433999,Human_RBP_ID_16699058,Human_RBP_ID_17056757,Human_RBP_ID_17065667,Human_RBP_ID_17070622,Human_RBP_ID_17174885,Human_RBP_ID_17202135,Human_RBP_ID_17322435,Human_RBP_ID_17436644,Human_RBP_ID_17550143,Human_RBP_ID_17716762,Human_RBP_ID_18137601,Human_RBP_ID_18185737,Human_RBP_ID_18203426,Human_RBP_ID_18212308,Human_RBP_ID_18453651,Human_RBP_ID_18521240,Human_RBP_ID_18542468,Human_RBP_ID_18909983,Human_RBP_ID_21659949,Human_RBP_ID_21955681,Human_RBP_ID_22118262,Human_RBP_ID_22341121,Human_RBP_ID_22411733,Human_RBP_ID_22838776,Human_RBP_ID_23095372,Human_RBP_ID_23141717,Human_RBP_ID_23201447,Human_RBP_ID_23300332,Human_RBP_ID_23316944,Human_RBP_ID_24307134,Human_RBP_ID_24442917,Human_RBP_ID_24523939,Human_RBP_ID_24537439,Human_RBP_ID_26243748,Human_RBP_ID_26564268,Human_RBP_ID_26739101,Human_RBP_ID_26752322,Human_RBP_ID_27137772,Human_RBP_ID_27162520,Human_RBP_ID_27376066,Human_RBP_ID_27546732,Human_RBP_ID_27570800,Human_RBP_ID_27786674 RMVar_hsa_circ_257216 65644 RMVar_ID_65644 Human_SNP_ID_403177843 m1A Human chr9 + 77177658 77177658 77177658 CCTCGAGGGAGGGGCGTGGGGAAGGCGGCGGGAGGAGGAGCGCACGGGCCGGCTGCCGTGCCCAC CCTCGAGGGAGGGGCGTGGGGAAGGCGGCGGGTGGAGGAGCGCACGGGCCGGCTGCCGTGCCCAC A T VPS13A Ensembl:ENSG00000197969 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:77177574..77177692 26863196 MeRIP-seq:(Medium) rs368715471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256921,Human_RBP_ID_798483,Human_RBP_ID_3975462,Human_RBP_ID_5036813,Human_RBP_ID_8239176,Human_RBP_ID_9338927,Human_RBP_ID_9441637,Human_RBP_ID_18427304,Human_RBP_ID_18506600,Human_RBP_ID_24563593,Human_RBP_ID_26360758 65645 RMVar_ID_65645 Human_SNP_ID_403240175 m1A Human chr9 + 77416254 77416254 77416254 TTACCCGGTTTTCTAAATTGAATCATGCATCTATTTATAATTCTAATTATTTTGTAAAAGAAGAC TTACCCGGTTTTCTAAATTGAATCATGCATCTGTTTATAATTCTAATTATTTTGTAAAAGAAGAC A G VPS13A Ensembl:ENSG00000197969 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:77416209..77416322 32194978 MeRIP-seq:(Medium) rs1171137090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1059638,Human_RBP_ID_3902445,Human_RBP_ID_7958095,Human_RBP_ID_9237540,Human_RBP_ID_27786726 Human_miRNA_ID_825420,Human_miRNA_ID_2349991 RMVar_hsa_circ_108882,RMVar_hsa_circ_257267 65646 RMVar_ID_65646 Human_SNP_ID_403352373 m1A Human chr9 - 77850217 77850217 77850217 AGGGCATTATTGACTCTGACAGATAAATGAGAAGAAAACCAGCTTCTGAGGGGTAGTGGAAGCAG AGGGCATTATTGACTCTGACAGATAAATGAGAGGAAAACCAGCTTCTGAGGGGTAGTGGAAGCAG T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:77850215..77850310 26863196 MeRIP-seq:(Medium) rs993748425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16701591 RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 65647 RMVar_ID_65647 Human_SNP_ID_403365399 m1A Human chr9 + 77901366 77901366 77901366 ACAGCCTTATCTCTCACCACAAAACCTGGCCCATCTGTGTATTTAGTCCCTAAATTACTCAACTT ACAGCCTTATCTCTCACCACAAAACCTGGCCCTTCTGTGTATTTAGTCCCTAAATTACTCAACTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:77901362..77901445 26863196 MeRIP-seq:(Medium) rs1038393161 Functional Loss SNV dbSNP153 33..33 33 - - - 65648 RMVar_ID_65648 Human_SNP_ID_403370413 m1A Human chr9 - 77922341 77922341 77922341 TGATGAGCTGCTATTGTTCATCTTTCAGGGACAGGAGAGAGTGGCAAGAGTACGTTTATCAAGCA TGATGAGCTGCTATTGTTCATCTTTCAGGGACGGGAGAGAGTGGCAAGAGTACGTTTATCAAGCA T C GNAQ Ensembl:ENSG00000156052 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:77922295..78031109 26863196 MeRIP-seq:(Medium) rs1428777047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27832414 Human_Splice_Rec_1054750,Human_Splice_Rec_1054762 RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280,RMVar_hsa_circ_257284,RMVar_hsa_circ_257286,RMVar_hsa_circ_257283,RMVar_hsa_circ_321071,RMVar_hsa_circ_257285 65649 RMVar_ID_65649 Human_SNP_ID_403389122 m1A Human chr9 - 77997322 77997322 77997322 TGGGTGGGAGGGCAGGCATGCTGATTGAATGTAGGAGGGGGCTGAAGGCCTTCTAATTGACATTT TGGGTGGGAGGGCAGGCATGCTGATTGAATGTGGGAGGGGGCTGAAGGCCTTCTAATTGACATTT T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:77997319..77997384 26863196 MeRIP-seq:(Medium) rs1030971289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24307693 65650 RMVar_ID_65650 Human_SNP_ID_403397370 m1A Human chr9 - 78030447 78030447 78030447 GGTCTGTGTACTGGGGGCGAGGCGGGAGGGCAAGCCCAAATGTGTCACACAAGTGCTGTTCTCTA GGTCTGTGTACTGGGGGCGAGGCGGGAGGGCACGCCCAAATGTGTCACACAAGTGCTGTTCTCTA T G GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:78030445..78030637 26863196 MeRIP-seq:(Medium) rs771628710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1118952,Human_RBP_ID_3908555,Human_RBP_ID_27137866 65651 RMVar_ID_65651 Human_SNP_ID_403448431 m1A Human chr9 - 78236328 78236328 78236328 AGTCGATCATGGCCCGAGGGCGGCCTCGGGGGATGCCCGCCGCGGAGACGCCGCCCGCGCCCACC AGTCGATCATGGCCCGAGGGCGGCCTCGGGGGCTGCCCGCCGCGGAGACGCCGCCCGCGCCCACC T G RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:78236129..78236400 26863410 MeRIP-seq:(Medium) rs973947175 Functional Loss SNV dbSNP153 33..33 33 - - - 65652 RMVar_ID_65652 Human_SNP_ID_403463506 m1A Human chr9 + 78297187 78297187 78297187 CAGCCGTTCACGCGTTCGGTCCTCCTTGGCTGACTCACCGCCCTGGCCGCCGCACCATGGACGCC CAGCCGTTCACGCGTTCGGTCCTCCTTGGCTGGCTCACCGCCCTGGCCGCCGCACCATGGACGCC A G PSAT1 Ensembl:ENSG00000135069 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:78297126..78297319;chr9:78297126..78297474;chr9:78297126..78297436 26863196 MeRIP-seq:(Medium) rs1282445750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1339509,Human_RBP_ID_1705958,Human_RBP_ID_5031875,Human_RBP_ID_5454665,Human_RBP_ID_5516339,Human_RBP_ID_8929177,Human_RBP_ID_9338933,Human_RBP_ID_16703513,Human_RBP_ID_18910221,Human_RBP_ID_26833271,Human_RBP_ID_27137907 Human_Splice_Rec_1055349,Human_Splice_Rec_1055365 RMVar_hsa_circ_85926,RMVar_hsa_circ_92519,RMVar_hsa_circ_257296,RMVar_hsa_circ_257297 65653 RMVar_ID_65653 Human_SNP_ID_403463509 m1A Human chr9 - 78297189 78297189 78297189 GGGGCGTCCATGGTGCGGCGGCCAGGGCGGTGAGTCAGCCAAGGAGGACCGAACGCGTGAACGGC GGGGCGTCCATGGTGCGGCGGCCAGGGCGGTGTGTCAGCCAAGGAGGACCGAACGCGTGAACGGC T A RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:78297126..78297320 26863196 MeRIP-seq:(Medium) rs1185593633 Functional Loss SNV dbSNP153 33..33 33 - - - 65654 RMVar_ID_65654 Human_SNP_ID_403463510 m1A Human chr9 - 78297189 78297189 78297189 GGGGCGTCCATGGTGCGGCGGCCAGGGCGGTGAGTCAGCCAAGGAGGACCGAACGCGTGAACGGC GGGGCGTCCATGGTGCGGCGGCCAGGGCGGTGGGTCAGCCAAGGAGGACCGAACGCGTGAACGGC T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:78297126..78297320 26863196 MeRIP-seq:(Medium) rs1185593633 Functional Loss SNV dbSNP153 33..33 33 - - - 65655 RMVar_ID_65655 Human_SNP_ID_403464507 m1A Human chr9 - 78300603 78300603 78300603 AGTCTAATAATTCCTTTTGTATCTCTAACAACACCTAGAAAAAAATAAAGGAAAATAGGGTTATT AGTCTAATAATTCCTTTTGTATCTCTAACAACTCCTAGAAAAAAATAAAGGAAAATAGGGTTATT T A RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:78300601..78300650 26863196 MeRIP-seq:(Medium) rs180707620 Functional Loss SNV dbSNP153 33..33 33 - - - 65656 RMVar_ID_65656 Human_SNP_ID_403464508 m1A Human chr9 - 78300603 78300603 78300603 AGTCTAATAATTCCTTTTGTATCTCTAACAACACCTAGAAAAAAATAAAGGAAAATAGGGTTATT AGTCTAATAATTCCTTTTGTATCTCTAACAACCCCTAGAAAAAAATAAAGGAAAATAGGGTTATT T G RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:78300601..78300650 26863196 MeRIP-seq:(Medium) rs180707620 Functional Loss SNV dbSNP153 33..33 33 - - - 65657 RMVar_ID_65657 Human_SNP_ID_403468124 m1A Human chr9 + 78314957 78314957 78314957 TGGTGACCTGGGCTCTGCTTGGATTCAATCACATGGCAGGGTGTGTTTCTGTGGTTCTGTGTGGA TGGTGACCTGGGCTCTGCTTGGATTCAATCACGTGGCAGGGTGTGTTTCTGTGGTTCTGTGTGGA A G PSAT1 Ensembl:ENSG00000135069 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:78314955..78315182 26863196 MeRIP-seq:(Medium) rs889323102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53541,RMVar_hsa_circ_108102,RMVar_hsa_circ_95463,RMVar_hsa_circ_257300,RMVar_hsa_circ_335340,RMVar_hsa_circ_257303,RMVar_hsa_circ_257305 65658 RMVar_ID_65658 Human_SNP_ID_403469542 m1A Human chr9 - 78320496 78320492 78320496 GAATGAGTGGATGGATGGATGGATGGATAGATAGATGGGTAGATAGGTGGAAGGGTGAATGAATA GAATGAGTGGATGGATGGATGGATGGATAGAT____GGGTAGATAGGTGGAAGGGTGAATGAATA CATCT C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:78320491..78320579 26863196 MeRIP-seq:(Medium) rs1465407889 Functional Loss DEL dbSNP153 33..36 33 - - - 65659 RMVar_ID_65659 Human_SNP_ID_403469543 m1A Human chr9 - 78320496 78320496 78320496 GAATGAGTGGATGGATGGATGGATGGATAGATAGATGGGTAGATAGGTGGAAGGGTGAATGAATA GAATGAGTGGATGGATGGATGGATGGATAGATGGATGGGTAGATAGGTGGAAGGGTGAATGAATA T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:78320491..78320579 26863196 MeRIP-seq:(Medium) rs998835826 Functional Loss SNV dbSNP153 33..33 33 - - - 65660 RMVar_ID_65660 Human_SNP_ID_403471760 m1A Human chr9 - 78329487 78329487 78329487 AATCAACAGCCGCTGAACCCAGGAGACCCCACAGATGTGTAGATTCAGCACCTAGAGGGCCCCCC AATCAACAGCCGCTGAACCCAGGAGACCCCACGGATGTGTAGATTCAGCACCTAGAGGGCCCCCC T C lnc-GNAQ-8,RF00017-4565 RNACentral:URS00008BFBF5,RNACentral:URS000096E4F6 lincRNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:78329438..78329563 26863196 MeRIP-seq:(Medium) rs1184969647 Functional Loss SNV dbSNP153 33..33 33 - - - 65661 RMVar_ID_65661 Human_SNP_ID_403795198 m1A Human chr9 + 79572092 79572088 79572093 GTTCGCAGAGTTTGAAAGGAGAGAGAATTAAAAAAAAAAGCCGCAAGCGTTTCACTCTTTTATTT GTTCGCAGAGTTTGAAAGGAGAGAGAATT_____AAAAAGCCGCAAGCGTTTCACTCTTTTATTT TAAAAA T TLE4 Ensembl:ENSG00000106829 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:79571992..79572103 26863410 MeRIP-seq:(Medium) rs1021967227 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_24308245,Human_RBP_ID_27137972 RMVar_hsa_circ_257309,RMVar_hsa_circ_113017 65662 RMVar_ID_65662 Human_SNP_ID_403795199 m1A Human chr9 + 79572092 79572088 79572093 GTTCGCAGAGTTTGAAAGGAGAGAGAATTAAAAAAAAAAGCCGCAAGCGTTTCACTCTTTTATTT GTTCGCAGAGTTTGAAAGGAGAGAGAATTA____AAAAAGCCGCAAGCGTTTCACTCTTTTATTT TAAAAA TA TLE4 Ensembl:ENSG00000106829 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:79571992..79572103 26863410 MeRIP-seq:(Medium) rs1021967227 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_24308245,Human_RBP_ID_27137972 RMVar_hsa_circ_257309,RMVar_hsa_circ_113017 65663 RMVar_ID_65663 Human_SNP_ID_403795200 m1A Human chr9 + 79572092 79572088 79572093 GTTCGCAGAGTTTGAAAGGAGAGAGAATTAAAAAAAAAAGCCGCAAGCGTTTCACTCTTTTATTT GTTCGCAGAGTTTGAAAGGAGAGAGAATTAA___AAAAAGCCGCAAGCGTTTCACTCTTTTATTT TAAAAA TAA TLE4 Ensembl:ENSG00000106829 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:79571992..79572103 26863410 MeRIP-seq:(Medium) rs1021967227 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_24308245,Human_RBP_ID_27137972 RMVar_hsa_circ_257309,RMVar_hsa_circ_113017 65664 RMVar_ID_65664 Human_SNP_ID_403795365 m1A Human chr9 + 79572547 79572547 79572547 GTCGGAGCGTTGCCTTGGGAGACGCGCGCCGGACAATGCCCGCGGCGGGCCAGTGACGCCCGCGG GTCGGAGCGTTGCCTTGGGAGACGCGCGCCGGGCAATGCCCGCGGCGGGCCAGTGACGCCCGCGG A G TLE4 Ensembl:ENSG00000106829 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:79572445..79572550 26863410 MeRIP-seq:(Medium) rs1449770105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257309,RMVar_hsa_circ_113017 65665 RMVar_ID_65665 Human_SNP_ID_403795470 m1A Human chr9 + 79572771 79572771 79572771 AAGCCAATGAGCCGCGCGCCTCTGCCGAGCGCAGCCAACTAAATCGGCTTGGATGATTCGCGACC AAGCCAATGAGCCGCGCGCCTCTGCCGAGCGCCGCCAACTAAATCGGCTTGGATGATTCGCGACC A C TLE4 Ensembl:ENSG00000106829 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:79572720..79572821 26863196 MeRIP-seq:(Medium) rs1366382185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16767038 Human_Splice_Rec_1055459,Human_Splice_Rec_1055497,Human_Splice_Rec_1055531,Human_Splice_Rec_1055539,Human_Splice_Rec_1055579,Human_Splice_Rec_1055597,Human_Splice_Rec_1055607,Human_Splice_Rec_1055647,Human_Splice_Rec_1055687,Human_Splice_Rec_1055695,Human_Splice_Rec_1055701,Human_Splice_Rec_1055705 RMVar_hsa_circ_257309,RMVar_hsa_circ_113017 65666 RMVar_ID_65666 Human_SNP_ID_404322954 m1A Human chr9 - 81634117 81634117 81634117 TCACTTGGCAATAAAAGATGACAAGAAGCACCACGATGCAGAGCACCACAGAGGTGAGAGGCCGG TCACTTGGCAATAAAAGATGACAAGAAGCACCGCGATGCAGAGCACCACAGAGGTGAGAGGCCGG T C TLE1 Ensembl:ENSG00000196781 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:81634066..81634156 32194978 MeRIP-seq:(Medium) rs375954684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1055901,Human_Splice_Rec_1055961 Human_miRNA_ID_2395189,Human_miRNA_ID_2907359,Human_miRNA_ID_3026195 RMVar_hsa_circ_99460,RMVar_hsa_circ_123217,RMVar_hsa_circ_268293,RMVar_hsa_circ_257343,RMVar_hsa_circ_118071,RMVar_hsa_circ_100025,RMVar_hsa_circ_257350,RMVar_hsa_circ_257352,RMVar_hsa_circ_82567,RMVar_hsa_circ_257351,RMVar_hsa_circ_257349,RMVar_hsa_circ_120012,RMVar_hsa_circ_368542,RMVar_hsa_circ_120710,RMVar_hsa_circ_118108,RMVar_hsa_circ_257356,RMVar_hsa_circ_257357,RMVar_hsa_circ_268632,RMVar_hsa_circ_101401,RMVar_hsa_circ_257359,RMVar_hsa_circ_330150,RMVar_hsa_circ_257360,RMVar_hsa_circ_95542,RMVar_hsa_circ_100826,RMVar_hsa_circ_105794,RMVar_hsa_circ_257361,RMVar_hsa_circ_257363,RMVar_hsa_circ_102848,RMVar_hsa_circ_257362,RMVar_hsa_circ_328541,RMVar_hsa_circ_257365,RMVar_hsa_circ_111407,RMVar_hsa_circ_257364,RMVar_hsa_circ_370901,RMVar_hsa_circ_257366 65667 RMVar_ID_65667 Human_SNP_ID_404339853 m1A Human chr9 + 81689255 81689255 81689255 ACCCGAGGGACGACATCCACGAGATGGTGGGGAAAACAGCAGGAGTGCGCTCCGCCAATCGGCCA ACCCGAGGGACGACATCCACGAGATGGTGGGGCAAACAGCAGGAGTGCGCTCCGCCAATCGGCCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:81688363..81689255 32194978 MeRIP-seq:(Medium) rs995624649 Functional Loss SNV dbSNP153 33..33 33 - - - 65668 RMVar_ID_65668 Human_SNP_ID_404339879 m1A Human chr9 + 81689324 81689324 81689324 CCCCGGCGGGCAAACTCTGCGGGCGAGTCCAGAGTAGTCACAGCGGTGGGGCCAGCGGGGGTTTT CCCCGGCGGGCAAACTCTGCGGGCGAGTCCAGGGTAGTCACAGCGGTGGGGCCAGCGGGGGTTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:81689273..81689529 26863196 MeRIP-seq:(Medium) rs1376576751 Functional Loss SNV dbSNP153 33..33 33 - - - 65669 RMVar_ID_65669 Human_SNP_ID_404339926 m1A Human chr9 - 81689437 81689437 81689437 GGCGGGTACTCTGTGCCCCGCGTCCCGGAGGCAGCCGACTGCGCCACCCCACCCTCGCACGGCCG GGCGGGTACTCTGTGCCCCGCGTCCCGGAGGCGGCCGACTGCGCCACCCCACCCTCGCACGGCCG T C TLE1 Ensembl:ENSG00000196781 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:81689337..81689500 26863196 MeRIP-seq:(Medium) rs1039991850 Functional Loss SNV dbSNP153 33..33 33 - - - 65670 RMVar_ID_65670 Human_SNP_ID_404707441 m1A Human chr9 + 83246620 83246620 83246620 TATAATGACCACCGCAAAACATGATCATGGACATGTATCAAAAAGCCATTCATATTCTCTCTCTC TATAATGACCACCGCAAAACATGATCATGGACGTGTATCAAAAAGCCATTCATATTCTCTCTCTC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:83246600..83246682 26863410 MeRIP-seq:(Medium) rs1047308223 Functional Loss SNV dbSNP153 33..33 33 - - - 65671 RMVar_ID_65671 Human_SNP_ID_404795884 m1A Human chr9 - 83623206 83623206 83623206 CCCTCTCCCGGACCTACTTCCCCGAGCCGCTCACGCCCATCACCAGCAGCGCGCCCGGCGCCGCC CCCTCTCCCGGACCTACTTCCCCGAGCCGCTCTCGCCCATCACCAGCAGCGCGCCCGGCGCCGCC T A RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:83622980..83623282 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 65672 RMVar_ID_65672 Human_SNP_ID_404800787 m1A Human chr9 + 83643487 83643486 83643488 TTCTAGCCTGTTCAGCCCTGAAGAAAACGTACAGAGACATATTAACACAAGGAAAAGATGGTGTA TTCTAGCCTGTTCAGCCCTGAAGAAAACGTAC__AGACATATTAACACAAGGAAAAGATGGTGTA CAG C IDNK Ensembl:ENSG00000148057 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:83643428..83643531 26863196 MeRIP-seq:(Medium) rs1459044285 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1056414,Human_Splice_Rec_1056422,Human_Splice_Rec_1056430,Human_Splice_Rec_1056438,Human_Splice_Rec_1056444,Human_Splice_Rec_1056450 65673 RMVar_ID_65673 Human_SNP_ID_404805567 m1A Human chr9 - 83661554 83661554 83661554 CTACTGCATGCATCACTTCTGCATTTATTGTAATTTTTTAAAAACATCACCTTTTATAGTTGGGT CTACTGCATGCATCACTTCTGCATTTATTGTAGTTTTTTAAAAACATCACCTTTTATAGTTGGGT T C UBQLN1 Ensembl:ENSG00000135018 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:83661355..83661555 32194978 MeRIP-seq:(Medium) rs1437475699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_720987,Human_RBP_ID_2065818,Human_RBP_ID_7940422,Human_RBP_ID_16718028,Human_RBP_ID_17436738,Human_RBP_ID_17550288,Human_RBP_ID_17716815,Human_RBP_ID_18138447,Human_RBP_ID_21906443,Human_RBP_ID_22838841,Human_RBP_ID_23093447,Human_RBP_ID_23300376,Human_RBP_ID_24442960,Human_RBP_ID_27787167 Human_miRNA_ID_860016 RMVar_hsa_circ_257402,RMVar_hsa_circ_100458,RMVar_hsa_circ_114557,RMVar_hsa_circ_257396,RMVar_hsa_circ_257397,RMVar_hsa_circ_257398,RMVar_hsa_circ_106466,RMVar_hsa_circ_268524,RMVar_hsa_circ_82923,RMVar_hsa_circ_84247,RMVar_hsa_circ_78767,RMVar_hsa_circ_257403,RMVar_hsa_circ_257400,RMVar_hsa_circ_257401,RMVar_hsa_circ_257399 65674 RMVar_ID_65674 Human_SNP_ID_404807689 m1A Human chr9 - 83669313 83669313 83669313 TTAAAAACAAACTTTCAGCTAGTATGTTCAACACACCAGGAATGCAGAGCTTGTTGCAACAAATA TTAAAAACAAACTTTCAGCTAGTATGTTCAACTCACCAGGAATGCAGAGCTTGTTGCAACAAATA T A UBQLN1 Ensembl:ENSG00000135018 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:83669263..83677925 32194978 MeRIP-seq:(Medium) rs1564160900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965788,Human_RBP_ID_2065836,Human_RBP_ID_7940497,Human_RBP_ID_16718283,Human_RBP_ID_17322912,Human_RBP_ID_22689979,Human_RBP_ID_26564398 Human_Splice_Rec_1056462,Human_Splice_Rec_1056480,Human_Splice_Rec_1056498 Human_miRNA_ID_2395191,Human_miRNA_ID_2977011 RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257402,RMVar_hsa_circ_114557,RMVar_hsa_circ_257397,RMVar_hsa_circ_257398,RMVar_hsa_circ_106466,RMVar_hsa_circ_268524,RMVar_hsa_circ_82923,RMVar_hsa_circ_84247,RMVar_hsa_circ_78767,RMVar_hsa_circ_257405,RMVar_hsa_circ_257400,RMVar_hsa_circ_257401,RMVar_hsa_circ_257399,RMVar_hsa_circ_376924,RMVar_hsa_circ_257404,RMVar_hsa_circ_335685,RMVar_hsa_circ_372418,RMVar_hsa_circ_278466,RMVar_hsa_circ_14758,RMVar_hsa_circ_257410,RMVar_hsa_circ_257407,RMVar_hsa_circ_257408,RMVar_hsa_circ_281760,RMVar_hsa_circ_367348,RMVar_hsa_circ_275132,RMVar_hsa_circ_99008,RMVar_hsa_circ_257409,RMVar_hsa_circ_21616,RMVar_hsa_circ_62064,RMVar_hsa_circ_285962,RMVar_hsa_circ_374410,RMVar_hsa_circ_257411,RMVar_hsa_circ_373398,RMVar_hsa_circ_116318,RMVar_hsa_circ_257414,RMVar_hsa_circ_257415,RMVar_hsa_circ_257413 65675 RMVar_ID_65675 Human_SNP_ID_404818015 m1A Human chr9 + 83707749 83707749 83707749 AGGAGGGAGCAGGCGAGCAAGGAGGAGCCAGCAGACACCAGAGCCGGCAGGCCTGGACAGCGAAG AGGAGGGAGCAGGCGAGCAAGGAGGAGCCAGCGGACACCAGAGCCGGCAGGCCTGGACAGCGAAG A G AL354920.1 Ensembl:ENSG00000254473 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:83707701..83707950 26863196 MeRIP-seq:(Medium) rs1229460402 Functional Loss SNV dbSNP153 33..33 33 - - - 65676 RMVar_ID_65676 Human_SNP_ID_404818088 m1A Human chr9 - 83707930 83707930 83707930 GGGCAGGGAGGAGGAAGCGGTGGCTGCTGCGGATGTCGGTGTGAGCGAGCGGCGCCTGAACACAC GGGCAGGGAGGAGGAAGCGGTGGCTGCTGCGGGTGTCGGTGTGAGCGAGCGGCGCCTGAACACAC T C UBQLN1 Ensembl:ENSG00000135018 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:83707781..83707975 26863196 MeRIP-seq:(Medium) rs1183902021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256634,Human_RBP_ID_796904,Human_RBP_ID_5032439,Human_RBP_ID_5329915,Human_RBP_ID_9315108,Human_RBP_ID_9338935,Human_RBP_ID_18427162,Human_RBP_ID_22466892 65677 RMVar_ID_65677 Human_SNP_ID_404818089 m1A Human chr9 - 83707930 83707930 83707930 GGGCAGGGAGGAGGAAGCGGTGGCTGCTGCGGATGTCGGTGTGAGCGAGCGGCGCCTGAACACAC GGGCAGGGAGGAGGAAGCGGTGGCTGCTGCGGCTGTCGGTGTGAGCGAGCGGCGCCTGAACACAC T G UBQLN1 Ensembl:ENSG00000135018 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:83707781..83707975 26863196 MeRIP-seq:(Medium) rs1183902021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256634,Human_RBP_ID_796904,Human_RBP_ID_5032439,Human_RBP_ID_5329915,Human_RBP_ID_9315108,Human_RBP_ID_9338935,Human_RBP_ID_18427162,Human_RBP_ID_22466892 65678 RMVar_ID_65678 Human_SNP_ID_404846432 m1A Human chr9 + 83817726 83817726 83817726 AACGGGTCCCGGGGCGCCGGGGCGGACCGCGGAGGTGAGCGCGGCTGCAGGCTGCGGTGAGGGGC AACGGGTCCCGGGGCGCCGGGGCGGACCGCGGCGGTGAGCGCGGCTGCAGGCTGCGGTGAGGGGC A C AL354733.1 Ensembl:ENSG00000226877 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:83817235..83817994 26863196 MeRIP-seq:(Medium) rs1181459305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1056601 65679 RMVar_ID_65679 Human_SNP_ID_404846433 m1A Human chr9 + 83817726 83817726 83817726 AACGGGTCCCGGGGCGCCGGGGCGGACCGCGGAGGTGAGCGCGGCTGCAGGCTGCGGTGAGGGGC AACGGGTCCCGGGGCGCCGGGGCGGACCGCGGGGGTGAGCGCGGCTGCAGGCTGCGGTGAGGGGC A G AL354733.1 Ensembl:ENSG00000226877 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:83817235..83817994 26863196 MeRIP-seq:(Medium) rs1181459305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1056601 65680 RMVar_ID_65680 Human_SNP_ID_404871711 m1A Human chr9 - 83921420 83921419 83921420 GCGGACGGCGGCTGCGCGGTGTGGCAGAGCGAAGCTGAGGAGTCCAGCGCTCGCCGACAGGGGCC GCGGACGGCGGCTGCGCGGTGTGGCAGAGCGA_GCTGAGGAGTCCAGCGCTCGCCGACAGGGGCC CT C KIF27 Ensembl:ENSG00000165115 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:83921083..83921523;chr9:83921260..83921505;chr9:83921358..83921453 26863196 MeRIP-seq:(Medium) rs1554691202 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1056727,Human_Splice_Rec_1056761,Human_Splice_Rec_1056793 RMVar_hsa_circ_257443,RMVar_hsa_circ_124334 65681 RMVar_ID_65681 Human_SNP_ID_404881286 m1A Human chr9 - 83956549 83956549 83956549 TCGTAGTAGCGCAAGGCGCAGAGTGGACCTTGACCCGCCTAGGGCGGGAAGAGTTTGGCCCGCCG TCGTAGTAGCGCAAGGCGCAGAGTGGACCTTGGCCCGCCTAGGGCGGGAAGAGTTTGGCCCGCCG T C C9orf64 Ensembl:ENSG00000165118 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:83956513..83956660 26863196 MeRIP-seq:(Medium) rs749750517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1706479,Human_RBP_ID_5036211,Human_RBP_ID_8930079,Human_RBP_ID_18138546,Human_RBP_ID_22466893 RMVar_hsa_circ_120606,RMVar_hsa_circ_257444 65682 RMVar_ID_65682 Human_SNP_ID_404884797 m1A Human chr9 + 83968612 83968611 83968613 ACTGCTCCCCACCTTAGTTCTTCACAACTAACATAGAAAATTGTTGAAAAGTAGGGGCAAGCATT ACTGCTCCCCACCTTAGTTCTTCACAACTAAC__AGAAAATTGTTGAAAAGTAGGGGCAAGCATT CAT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:83968429..83968728 32194978 MeRIP-seq:(Medium) rs1165250339 Functional Loss DEL dbSNP153 33..34 33 - - - 65683 RMVar_ID_65683 Human_SNP_ID_404885830 m1A Human chr9 - 83971637 83971637 83971637 AAGAACTTTGGTTTATTACCAGTGTGTTGGGTATGTGAGGGTTGTCACAATGTAGTTCACGTTTT AAGAACTTTGGTTTATTACCAGTGTGTTGGGTGTGTGAGGGTTGTCACAATGTAGTTCACGTTTT T C HNRNPK Ensembl:ENSG00000165119 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:83971635..83971769 26863196 MeRIP-seq:(Medium) rs1432354214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070453,Human_RBP_ID_5407753,Human_RBP_ID_8707194,Human_RBP_ID_9351730,Human_RBP_ID_17642999,Human_RBP_ID_19145115,Human_RBP_ID_22368436,Human_RBP_ID_22689989,Human_RBP_ID_23259640,Human_RBP_ID_24524103 Human_Splice_Rec_1056876,Human_Splice_Rec_1056908,Human_Splice_Rec_1056938,Human_Splice_Rec_1056970,Human_Splice_Rec_1057014 RMVar_hsa_circ_18792,RMVar_hsa_circ_51806,RMVar_hsa_circ_92761,RMVar_hsa_circ_96496,RMVar_hsa_circ_126315,RMVar_hsa_circ_102342,RMVar_hsa_circ_257448,RMVar_hsa_circ_257449,RMVar_hsa_circ_257447,RMVar_hsa_circ_257450 65684 RMVar_ID_65684 Human_SNP_ID_404885982 m1A Human chr9 - 83971990 83971988 83971991 TCCCATGCCTCCATCTAGAAGAGATTATGATGATATGAGCCCTCGTCGAGGACCACCTCCCCCTC TCCCATGCCTCCATCTAGAAGAGATTATGAT___ATGAGCCCTCGTCGAGGACCACCTCCCCCTC TATC T HNRNPK Ensembl:ENSG00000165119 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:83971940..83972062 26863196 MeRIP-seq:(Medium) rs758707867 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1403671,Human_RBP_ID_1706523,Human_RBP_ID_7941017,Human_RBP_ID_9238125,Human_RBP_ID_16719656,Human_RBP_ID_18138579,Human_RBP_ID_18910730,Human_RBP_ID_22466902,Human_RBP_ID_22534463,Human_RBP_ID_24309936 RMVar_hsa_circ_18792,RMVar_hsa_circ_51806,RMVar_hsa_circ_26660,RMVar_hsa_circ_92761,RMVar_hsa_circ_96496,RMVar_hsa_circ_126315,RMVar_hsa_circ_102342,RMVar_hsa_circ_257448,RMVar_hsa_circ_257449,RMVar_hsa_circ_257447,RMVar_hsa_circ_77813,RMVar_hsa_circ_257450,RMVar_hsa_circ_12104,RMVar_hsa_circ_93951,RMVar_hsa_circ_257451,RMVar_hsa_circ_26918,RMVar_hsa_circ_257452 65685 RMVar_ID_65685 Human_SNP_ID_404886844 m1A Human chr9 - 83974588 83974588 83974588 TGTACTATCTGGTATTTGTGGTGTTTGACAGCATATTGAGTATCAGTGCTGATATTGAAACAATT TGTACTATCTGGTATTTGTGGTGTTTGACAGCGTATTGAGTATCAGTGCTGATATTGAAACAATT T C HNRNPK Ensembl:ENSG00000165119 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:83974551..83974600 26863196 MeRIP-seq:(Medium) rs1382108326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91635,Human_RBP_ID_721108,Human_RBP_ID_964565,Human_RBP_ID_1706542,Human_RBP_ID_2065925,Human_RBP_ID_3222218,Human_RBP_ID_9351918,Human_RBP_ID_9406981,Human_RBP_ID_18140817,Human_RBP_ID_18910742,Human_RBP_ID_22341433,Human_RBP_ID_24309953,Human_RBP_ID_26231569 Human_Splice_Rec_1056866,Human_Splice_Rec_1056867,Human_Splice_Rec_1056898,Human_Splice_Rec_1056899,Human_Splice_Rec_1056928,Human_Splice_Rec_1056929,Human_Splice_Rec_1056960,Human_Splice_Rec_1056961,Human_Splice_Rec_1057006,Human_Splice_Rec_1057007,Human_Splice_Rec_1057032,Human_Splice_Rec_1057033,Human_Splice_Rec_1057040,Human_Splice_Rec_1057041 RMVar_hsa_circ_18792,RMVar_hsa_circ_12324,RMVar_hsa_circ_92761,RMVar_hsa_circ_96496,RMVar_hsa_circ_126315,RMVar_hsa_circ_257448,RMVar_hsa_circ_257449,RMVar_hsa_circ_257447,RMVar_hsa_circ_77813,RMVar_hsa_circ_64103,RMVar_hsa_circ_12104,RMVar_hsa_circ_257451,RMVar_hsa_circ_370720,RMVar_hsa_circ_257454 65686 RMVar_ID_65686 Human_SNP_ID_404887997 m1A Human chr9 - 83978281 83978280 83978282 AGCCAAATGTACTAGCTGCTTTATTTTTCCACAGATTGGTGTGCCCGTTTAATAAAAGAATATGG AGCCAAATGTACTAGCTGCTTTATTTTTCCA__GATTGGTGTGCCCGTTTAATAAAAGAATATGG CTG C HNRNPK Ensembl:ENSG00000165119 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:83978258..83978357 26863196 MeRIP-seq:(Medium) rs758327129 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1403672,Human_RBP_ID_5407762,Human_RBP_ID_19145120,Human_RBP_ID_22627711,Human_RBP_ID_22691153,Human_RBP_ID_26231686 Human_Splice_Rec_1056859,Human_Splice_Rec_1056891,Human_Splice_Rec_1056921,Human_Splice_Rec_1056953,Human_Splice_Rec_1056999,Human_Splice_Rec_1057027,Human_Splice_Rec_1057049 RMVar_hsa_circ_18792,RMVar_hsa_circ_12324,RMVar_hsa_circ_92761,RMVar_hsa_circ_257447,RMVar_hsa_circ_310635,RMVar_hsa_circ_295988 65687 RMVar_ID_65687 Human_SNP_ID_404888433 m1A Human chr9 + 83979534 83979534 83979534 GCCAACGCGCCCTCCCCTCCCCGCCTCCCGGCACCGAGATCAAAAACAGCCGGGTAACAGGACGG GCCAACGCGCCCTCCCCTCCCCGCCTCCCGGCCCCGAGATCAAAAACAGCCGGGTAACAGGACGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:83979529..83979649 26863196 MeRIP-seq:(Medium) rs1407369328 Functional Loss SNV dbSNP153 33..33 33 - - - 65688 RMVar_ID_65688 Human_SNP_ID_404888693 m1A Human chr9 - 83980072 83980072 83980072 CCAGTTTTTCCGCTTGAGGGAGGCGTCCTGGGAGCCGCTTTGGTGTTTGGCCGCTTCTCCGAGTG CCAGTTTTTCCGCTTGAGGGAGGCGTCCTGGGTGCCGCTTTGGTGTTTGGCCGCTTCTCCGAGTG T A HNRNPK Ensembl:ENSG00000165119 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:83980067..83980225 26863410 MeRIP-seq:(Medium) rs1202842794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906284,Human_RBP_ID_5244099,Human_RBP_ID_5407243,Human_RBP_ID_7941091,Human_RBP_ID_17176459,Human_RBP_ID_18506610,Human_RBP_ID_22627714 RMVar_hsa_circ_92761,RMVar_hsa_circ_257447 65689 RMVar_ID_65689 Human_SNP_ID_404889080 m1A Human chr9 - 83980833 83980833 83980833 AACATCGGTCCCTGGGCAGCGCAACTGTAAGGACAGGAACCGCCGCGGCGCGCTCCCAGTTCCTT AACATCGGTCCCTGGGCAGCGCAACTGTAAGGCCAGGAACCGCCGCGGCGCGCTCCCAGTTCCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:83980783..83980944 26863196 MeRIP-seq:(Medium) rs1430807684 Functional Loss SNV dbSNP153 33..33 33 - - - 65690 RMVar_ID_65690 Human_SNP_ID_404889085 m1A Human chr9 + 83980840 83980840 83980840 TGGGAGCGCGCCGCGGCGGTTCCTGTCCTTACAGTTGCGCTGCCCAGGGACCGATGTTGCGCGAG TGGGAGCGCGCCGCGGCGGTTCCTGTCCTTACCGTTGCGCTGCCCAGGGACCGATGTTGCGCGAG A C RMI1 Ensembl:ENSG00000178966 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:83980789..83980899 26863196 MeRIP-seq:(Medium) rs1564075534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5032598,Human_RBP_ID_18427164 Human_Splice_Rec_1057055 65691 RMVar_ID_65691 Human_SNP_ID_404891550 m1A Human chr9 + 83990154 83990154 83990154 AAGTTGATCTCGGGAAGGTAGAGAGTAGAACAATGGTTACCAGAGGCTGGGAAGGGTAGGGGGGC AAGTTGATCTCGGGAAGGTAGAGAGTAGAACAGTGGTTACCAGAGGCTGGGAAGGGTAGGGGGGC A G RMI1 Ensembl:ENSG00000178966 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:83990149..83990240 26863196 MeRIP-seq:(Medium) rs553848773 Functional Loss SNV dbSNP153 33..33 33 - - - 65692 RMVar_ID_65692 Human_SNP_ID_405306008 m1A Human chr9 + 85716864 85716863 85716864 AATGACATAAAAGACCCTAGAGGAATACCCCCAGTCCTTACCTCCCTGTCTTCATATCCTACCTA AATGACATAAAAGACCCTAGAGGAATACCCCC_GTCCTTACCTCCCTGTCTTCATATCCTACCTA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85716858..85716975 26863196 MeRIP-seq:(Medium) rs1305802753 Functional Loss DEL dbSNP153 33..33 33 - - - 65693 RMVar_ID_65693 Human_SNP_ID_405306010 m1A Human chr9 + 85716864 85716864 85716864 AATGACATAAAAGACCCTAGAGGAATACCCCCAGTCCTTACCTCCCTGTCTTCATATCCTACCTA AATGACATAAAAGACCCTAGAGGAATACCCCCGGTCCTTACCTCCCTGTCTTCATATCCTACCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85716858..85716975 26863196 MeRIP-seq:(Medium) rs1442208922 Functional Loss SNV dbSNP153 33..33 33 - - - 65694 RMVar_ID_65694 Human_SNP_ID_405312188 m1A Human chr9 + 85741828 85741828 85741828 CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCAGCACCTGGATCACGGCGGATCCCTCGCCGCCC CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCCGCACCTGGATCACGGCGGATCCCTCGCCGCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85741744..85741902 26863196 MeRIP-seq:(Medium) rs10114347 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7918 65695 RMVar_ID_65695 Human_SNP_ID_405312189 m1A Human chr9 + 85741828 85741828 85741828 CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCAGCACCTGGATCACGGCGGATCCCTCGCCGCCC CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCGGCACCTGGATCACGGCGGATCCCTCGCCGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85741744..85741902 26863196 MeRIP-seq:(Medium) rs10114347 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7918 65696 RMVar_ID_65696 Human_SNP_ID_405312190 m1A Human chr9 + 85741828 85741828 85741828 CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCAGCACCTGGATCACGGCGGATCCCTCGCCGCCC CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCTGCACCTGGATCACGGCGGATCCCTCGCCGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85741744..85741902 26863196 MeRIP-seq:(Medium) rs10114347 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7918 65697 RMVar_ID_65697 Human_SNP_ID_405312197 m1A Human chr9 - 85741848 85741848 85741848 GTATGAAAACACCGGGCGGCGGGCGGCGAGGGATCCGCCGTGATCCAGGTGCTGAGCCGGGTGCT GTATGAAAACACCGGGCGGCGGGCGGCGAGGGCTCCGCCGTGATCCAGGTGCTGAGCCGGGTGCT T G AGTPBP1 Ensembl:ENSG00000135049 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:85741792..85741877 26863410 MeRIP-seq:(Medium) rs1366183110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1057427,Human_Splice_Rec_1057477,Human_Splice_Rec_1057525,Human_Splice_Rec_1057575,Human_Splice_Rec_1057627 65698 RMVar_ID_65698 Human_SNP_ID_405360041 m1A Human chr9 + 85941238 85941238 85941238 CGAGGCGGCGTCGTTATTTCCGTGGTCCGGACAGTGCGTGGCGGCGCGGGTGACCACGGGAGAAG CGAGGCGGCGTCGTTATTTCCGTGGTCCGGACGGTGCGTGGCGGCGCGGGTGACCACGGGAGAAG A G NAA35 Ensembl:ENSG00000135040 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:85941120..85941414 26863196 MeRIP-seq:(Medium) rs544193368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798701,Human_RBP_ID_5043637,Human_RBP_ID_18427165 Human_Splice_Rec_1057915,Human_Splice_Rec_1057959 65699 RMVar_ID_65699 Human_SNP_ID_405360336 m1A Human chr9 + 85942203 85942203 85942203 AGCTTCTGTAGATGATGACGATTCAGGATGGGAGCTCAGTATGCCAGAAAAAATGGAGAAAAGCA AGCTTCTGTAGATGATGACGATTCAGGATGGGGGCTCAGTATGCCAGAAAAAATGGAGAAAAGCA A G NAA35 Ensembl:ENSG00000135040 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:85942130..85942224;chr9:85941849..85958483 26863196 MeRIP-seq:(Medium) rs760110240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5032833,Human_RBP_ID_16722672,Human_RBP_ID_18427166,Human_RBP_ID_23093635,Human_RBP_ID_24310899 Human_Splice_Rec_1057916,Human_Splice_Rec_1057917,Human_Splice_Rec_1057960,Human_Splice_Rec_1057961,Human_Splice_Rec_1057972,Human_Splice_Rec_1057973 Human_miRNA_ID_2214238 RMVar_hsa_circ_45058,RMVar_hsa_circ_96864,RMVar_hsa_circ_257574 65700 RMVar_ID_65700 Human_SNP_ID_405381587 m1A Human chr9 + 86028085 86028085 86028085 GATGGCAACGGTGATATGGGAGGGGGACAGGGAAGTGCTGGGTAGAGAAGGGCAGGGTCACTGGC GATGGCAACGGTGATATGGGAGGGGGACAGGGCAGTGCTGGGTAGAGAAGGGCAGGGTCACTGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:86028083..86028167 26863196 MeRIP-seq:(Medium) rs949158224 Functional Loss SNV dbSNP153 33..33 33 - - - 65701 RMVar_ID_65701 Human_SNP_ID_405383197 m1A Human chr9 + 86033364 86033364 86033364 GATTCTGCTTCATTTTCATCCATGTTGTAGTCATCTTCTCCTCTCAGTTTCTGCTGGTTTCTCCC GATTCTGCTTCATTTTCATCCATGTTGTAGTCGTCTTCTCCTCTCAGTTTCTGCTGGTTTCTCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86033313..86033444 26863196 MeRIP-seq:(Medium) rs765661815 Functional Loss SNV dbSNP153 33..33 33 - - - 65702 RMVar_ID_65702 Human_SNP_ID_405383800 m1A Human chr9 + 86035496 86035496 86035496 ACAGGGCAGCCTGCACCTGTGGGGTCTGGCCCAGTTCTCCGGCTCCCCCGAAGCCTCTTCCACCT ACAGGGCAGCCTGCACCTGTGGGGTCTGGCCCTGTTCTCCGGCTCCCCCGAAGCCTCTTCCACCT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:86035376..86035600 26863196 MeRIP-seq:(Medium) rs1486858485 Functional Loss SNV dbSNP153 33..33 33 - - - 65703 RMVar_ID_65703 Human_SNP_ID_405384135 m1A Human chr9 - 86036297 86036297 86036297 TTGCCCTGTTCCCAGCTCTCCAGAGCCCCATCAGAGGAAGCAGTCCCAGCGAGCTGCTGAGGCAG TTGCCCTGTTCCCAGCTCTCCAGAGCCCCATCGGAGGAAGCAGTCCCAGCGAGCTGCTGAGGCAG T C GOLM1 Ensembl:ENSG00000135052 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86036295..86036548 26863196 MeRIP-seq:(Medium) rs1346418846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257602,RMVar_hsa_circ_275985,RMVar_hsa_circ_297370,RMVar_hsa_circ_299014,RMVar_hsa_circ_282500,RMVar_hsa_circ_66573,RMVar_hsa_circ_257600,RMVar_hsa_circ_257601,RMVar_hsa_circ_346381,RMVar_hsa_circ_257599,RMVar_hsa_circ_257603 65704 RMVar_ID_65704 Human_SNP_ID_405384185 m1A Human chr9 - 86036402 86036402 86036402 AGGGAAACGTGCTTGGTAACAGCAAGTCCCAGACACCAGCCCCCAGTTCCGAAGTGGTTTTGGAT AGGGAAACGTGCTTGGTAACAGCAAGTCCCAGGCACCAGCCCCCAGTTCCGAAGTGGTTTTGGAT T C GOLM1 Ensembl:ENSG00000135052 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:86036351..86036518 32194978 MeRIP-seq:(Medium) rs1163949882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1058003,Human_Splice_Rec_1058019,Human_Splice_Rec_1058025,Human_Splice_Rec_1058035 RMVar_hsa_circ_1616,RMVar_hsa_circ_257602,RMVar_hsa_circ_275985,RMVar_hsa_circ_297370,RMVar_hsa_circ_299014,RMVar_hsa_circ_282500,RMVar_hsa_circ_66573,RMVar_hsa_circ_257600,RMVar_hsa_circ_257601,RMVar_hsa_circ_346381,RMVar_hsa_circ_257599,RMVar_hsa_circ_257603 65705 RMVar_ID_65705 Human_SNP_ID_405385429 m1A Human chr9 - 86040801 86040801 86040801 AACAGTGTGAGGAGCGAATAGAAGAGGTCACCAAAAAGGGGAATGAAGCTGTAGCTTCCAGAGAC AACAGTGTGAGGAGCGAATAGAAGAGGTCACCGAAAAGGGGAATGAAGCTGTAGCTTCCAGAGAC T C GOLM1 Ensembl:ENSG00000135052 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86040697..86040818 26863196 MeRIP-seq:(Medium) rs773222323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2066254,Human_RBP_ID_5032988,Human_RBP_ID_23093701 Human_Splice_Rec_1058000,Human_Splice_Rec_1058001,Human_Splice_Rec_1058016,Human_Splice_Rec_1058017,Human_Splice_Rec_1058032,Human_Splice_Rec_1058033,Human_Splice_Rec_1058040 RMVar_hsa_circ_1616,RMVar_hsa_circ_275985,RMVar_hsa_circ_297370,RMVar_hsa_circ_282500,RMVar_hsa_circ_66573,RMVar_hsa_circ_257600,RMVar_hsa_circ_257601,RMVar_hsa_circ_346381,RMVar_hsa_circ_257599,RMVar_hsa_circ_257603,RMVar_hsa_circ_257605,RMVar_hsa_circ_270964,RMVar_hsa_circ_295778,RMVar_hsa_circ_337679,RMVar_hsa_circ_257606,RMVar_hsa_circ_257604 65706 RMVar_ID_65706 Human_SNP_ID_405388655 m1A Human chr9 + 86052862 86052862 86052862 CCCCACTCCAGCCCAGGAAACGCTGCTCCTCCAGGAAAGGGCCAGCCAGGCCCTCCTTCCTCCTG CCCCACTCCAGCCCAGGAAACGCTGCTCCTCCGGGAAAGGGCCAGCCAGGCCCTCCTTCCTCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:86052858..86053878 26863196 MeRIP-seq:(Medium) rs570912030 Functional Loss SNV dbSNP153 33..33 33 - - - 65707 RMVar_ID_65707 Human_SNP_ID_405388672 m1A Human chr9 + 86052925 86052925 86052925 TGCCCGACACAGCAGAGGCTCTGGGCACCCAGAGGGCTAATCAGCAACCTCACACCGCACCACAC TGCCCGACACAGCAGAGGCTCTGGGCACCCAGTGGGCTAATCAGCAACCTCACACCGCACCACAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:86052922..86053127 26863196 MeRIP-seq:(Medium) rs1347755908 Functional Loss SNV dbSNP153 33..33 33 - - - 65708 RMVar_ID_65708 Human_SNP_ID_405389201 m1A Human chr9 - 86053626 86053624 86053626 GTGTAGCATGGTGTGGTGTGTGTTTTGTAGTGATGTTTGGTGTGGTGTGTGATGTGTGTGTGGAG GTGTAGCATGGTGTGGTGTGTGTTTTGTAGTG__GTTTGGTGTGGTGTGTGATGTGTGTGTGGAG CAT C GOLM1 Ensembl:ENSG00000135052 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86053616..86053696 26863196 MeRIP-seq:(Medium) rs1376965789 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_66573,RMVar_hsa_circ_337679,RMVar_hsa_circ_257606,RMVar_hsa_circ_328380 65709 RMVar_ID_65709 Human_SNP_ID_405389205 m1A Human chr9 - 86053626 86053625 86053626 GTGTAGCATGGTGTGGTGTGTGTTTTGTAGTGATGTTTGGTGTGGTGTGTGATGTGTGTGTGGAG GTGTAGCATGGTGTGGTGTGTGTTTTGTAGTG_TGTTTGGTGTGGTGTGTGATGTGTGTGTGGAG AT A GOLM1 Ensembl:ENSG00000135052 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86053616..86053696 26863196 MeRIP-seq:(Medium) rs1564347491 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_66573,RMVar_hsa_circ_337679,RMVar_hsa_circ_257606,RMVar_hsa_circ_328380 65710 RMVar_ID_65710 Human_SNP_ID_405389251 m1A Human chr9 - 86053662 86053662 86053662 GTGGTGTGTGTGGAGTGGTGTGCCGTGTGTGGAGTGGTGTAGCATGGTGTGGTGTGTGTTTTGTA GTGGTGTGTGTGGAGTGGTGTGCCGTGTGTGGTGTGGTGTAGCATGGTGTGGTGTGTGTTTTGTA T A GOLM1 Ensembl:ENSG00000135052 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:86053611..86053789 26863196 MeRIP-seq:(Medium) rs58785058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66573,RMVar_hsa_circ_337679,RMVar_hsa_circ_257606,RMVar_hsa_circ_328380 65711 RMVar_ID_65711 Human_SNP_ID_405392399 m1A Human chr9 + 86064365 86064365 86064365 TGGATTTTACTGACCTGCTTCCATTCTGCTCAATTCACACTTTCCCGCACCTATCCCATCTGTCA TGGATTTTACTGACCTGCTTCCATTCTGCTCACTTCACACTTTCCCGCACCTATCCCATCTGTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:86064363..86064540 26863196 MeRIP-seq:(Medium) rs1275492486 Functional Loss SNV dbSNP153 33..33 33 - - - 65712 RMVar_ID_65712 Human_SNP_ID_405449665 m1A Human chr9 - 86297854 86297854 86297854 TGAAGTCAGAGGGTGGATAGATCTGGGTTATGAAGCGCCTTCAGCAGTGGTAGGTACCGTTTTTG TGAAGTCAGAGGGTGGATAGATCTGGGTTATGGAGCGCCTTCAGCAGTGGTAGGTACCGTTTTTG T C TUT7 Ensembl:ENSG00000083223 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:86297804..86298155 26863196 MeRIP-seq:(Medium) rs1229901333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105154,RMVar_hsa_circ_257610 65713 RMVar_ID_65713 Human_SNP_ID_405455539 m1A Human chr9 - 86323106 86323106 86323106 ATGGCATGGCTAATGAAGATGAGTTAGACAACACCTACACTGGGTCAGGGGATGAGGACGCCCTA ATGGCATGGCTAATGAAGATGAGTTAGACAACTCCTACACTGGGTCAGGGGATGAGGACGCCCTA T A TUT7 Ensembl:ENSG00000083223 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:86323055..86323140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22119282,Human_RBP_ID_24549599,Human_RBP_ID_27833132 RMVar_hsa_circ_367806,RMVar_hsa_circ_63121,RMVar_hsa_circ_53082,RMVar_hsa_circ_55923,RMVar_hsa_circ_30555,RMVar_hsa_circ_257612,RMVar_hsa_circ_58537,RMVar_hsa_circ_359058,RMVar_hsa_circ_359751,RMVar_hsa_circ_47200,RMVar_hsa_circ_257620,RMVar_hsa_circ_353569,RMVar_hsa_circ_257622,RMVar_hsa_circ_322445,RMVar_hsa_circ_257623,RMVar_hsa_circ_355889,RMVar_hsa_circ_361843,RMVar_hsa_circ_14937,RMVar_hsa_circ_266681,RMVar_hsa_circ_354884 65714 RMVar_ID_65714 Human_SNP_ID_405455631 m1A Human chr9 - 86323358 86323358 86323358 TGGATTTAGAAGGCTTCCAAAATCCCACAGCTAAAGAGTGTGAGGGACTTGCCACTTTAGATAAC TGGATTTAGAAGGCTTCCAAAATCCCACAGCTGAAGAGTGTGAGGGACTTGCCACTTTAGATAAC T C TUT7 Ensembl:ENSG00000083223 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:86323309..86323387 32194978 MeRIP-seq:(Medium) rs1186778073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26361793 RMVar_hsa_circ_367806,RMVar_hsa_circ_63121,RMVar_hsa_circ_53082,RMVar_hsa_circ_55923,RMVar_hsa_circ_30555,RMVar_hsa_circ_257612,RMVar_hsa_circ_58537,RMVar_hsa_circ_359058,RMVar_hsa_circ_359751,RMVar_hsa_circ_47200,RMVar_hsa_circ_257620,RMVar_hsa_circ_353569,RMVar_hsa_circ_257622,RMVar_hsa_circ_322445,RMVar_hsa_circ_257623,RMVar_hsa_circ_355889,RMVar_hsa_circ_361843,RMVar_hsa_circ_14937,RMVar_hsa_circ_266681,RMVar_hsa_circ_354884 65715 RMVar_ID_65715 Human_SNP_ID_405462755 m1A Human chr9 - 86354342 86354342 86354342 GCTCTTGGGCGCCTTCTCCCAACGTCCCTGCCAGACTCGCCTCCGGGCTGATTCTCCAGTTGGTT GCTCTTGGGCGCCTTCTCCCAACGTCCCTGCCGGACTCGCCTCCGGGCTGATTCTCCAGTTGGTT T C TUT7 Ensembl:ENSG00000083223 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:86354292..86354426 26863196 MeRIP-seq:(Medium) rs1239746373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036221,Human_RBP_ID_9315111,Human_RBP_ID_18911040 Human_Splice_Rec_1058111,Human_Splice_Rec_1058165,Human_Splice_Rec_1058217 65716 RMVar_ID_65716 Human_SNP_ID_405462771 m1A Human chr9 + 86354382 86354382 86354382 ACGTTGGGAGAAGGCGCCCAAGAGCACTCACCACCTTCGCCGCGGTCCCCAGCCTCTTCCTGTCC ACGTTGGGAGAAGGCGCCCAAGAGCACTCACCGCCTTCGCCGCGGTCCCCAGCCTCTTCCTGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86354333..86354426 26863196 MeRIP-seq:(Medium) rs1185096410 Functional Loss SNV dbSNP153 33..33 33 - - - 65717 RMVar_ID_65717 Human_SNP_ID_405462773 m1A Human chr9 - 86354385 86354385 86354385 CCGGGACAGGAAGAGGCTGGGGACCGCGGCGAAGGTGGTGAGTGCTCTTGGGCGCCTTCTCCCAA CCGGGACAGGAAGAGGCTGGGGACCGCGGCGAGGGTGGTGAGTGCTCTTGGGCGCCTTCTCCCAA T C TUT7 Ensembl:ENSG00000083223 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:86354304..86354467 26863196 MeRIP-seq:(Medium) rs1040197150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9315111 65718 RMVar_ID_65718 Human_SNP_ID_405610615 m1A Human chr9 + 86946292 86946292 86946292 CGCAGCGCCGCCGGGCCTCGGTGCAGCCCATGACCCCGCCCGCGCCGGGGCCGCCCGCGCCGCCG CGCAGCGCCGCCGGGCCTCGGTGCAGCCCATGCCCCCGCCCGCGCCGGGGCCGCCCGCGCCGCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:86946256..86946539 26863196 MeRIP-seq:(Medium) rs896991763 Functional Loss SNV dbSNP153 33..33 33 - - - 65719 RMVar_ID_65719 Human_SNP_ID_405658810 m1A Human chr9 - 87148593 87148593 87148593 TTTTTCTCGCTCTCTCTCGCCGTTCCCCGGGCAGGCAGCGTCTGCTTTTCAGCGCGCGGACATTT TTTTTCTCGCTCTCTCTCGCCGTTCCCCGGGCGGGCAGCGTCTGCTTTTCAGCGCGCGGACATTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:87148551..87148729 26863196 MeRIP-seq:(Medium) rs930617401 Functional Loss SNV dbSNP153 33..33 33 - - - 65720 RMVar_ID_65720 Human_SNP_ID_405743638 m1A Human chr9 + 87497764 87497764 87497764 GCGCAGAACCCGCAGCGCCGGCCTGGCAGGGCAGCTCGGAGGTGGGTGGGCCGCGCCGCCAGCCC GCGCAGAACCCGCAGCGCCGGCCTGGCAGGGCGGCTCGGAGGTGGGTGGGCCGCGCCGCCAGCCC A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:87497656..87497855 26863196 MeRIP-seq:(Medium) rs1238578107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22627737 Human_Splice_Rec_1058399 65721 RMVar_ID_65721 Human_SNP_ID_405743646 m1A Human chr9 + 87497771 87497771 87497771 ACCCGCAGCGCCGGCCTGGCAGGGCAGCTCGGAGGTGGGTGGGCCGCGCCGCCAGCCCGCTTGCA ACCCGCAGCGCCGGCCTGGCAGGGCAGCTCGGGGGTGGGTGGGCCGCGCCGCCAGCCCGCTTGCA A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:87497639..87498080 26863196 MeRIP-seq:(Medium) rs961333508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036222,Human_RBP_ID_22627737 Human_Splice_Rec_1058399 65722 RMVar_ID_65722 Human_SNP_ID_405743759 m1A Human chr9 + 87497978 87497978 87497978 CGCAGCGGCAGGGTCTGGGGCCGGCGCCTGGGAGGGATCTGCGCCCCCCACTCACTCCCTAGCTG CGCAGCGGCAGGGTCTGGGGCCGGCGCCTGGGGGGGATCTGCGCCCCCCACTCACTCCCTAGCTG A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:87497953..87498104 26863196 MeRIP-seq:(Medium) rs2302791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035736,Human_RBP_ID_9408139,Human_RBP_ID_18427169 65723 RMVar_ID_65723 Human_SNP_ID_405750907 m1A Human chr9 + 87525479 87525479 87525479 AGGATATCGGTTTCATTAAGTTGGACTAAATGATCTTCCTTCAAAGGATTATCCAAGGCATATAC AGGATATCGGTTTCATTAAGTTGGACTAAATGCTCTTCCTTCAAAGGATTATCCAAGGCATATAC A C DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879184341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26566869 RMVar_hsa_circ_257632,RMVar_hsa_circ_122387,RMVar_hsa_circ_349031,RMVar_hsa_circ_373594,RMVar_hsa_circ_337567,RMVar_hsa_circ_70360,RMVar_hsa_circ_257633,RMVar_hsa_circ_257634,RMVar_hsa_circ_257631 65724 RMVar_ID_65724 Human_SNP_ID_405777268 m1A Human chr9 - 87632777 87632777 87632777 TCATCCCTACATATACACTGATTCTCCTTCATATCTACATATATACTCATCCTCCTTCTTCCCTA TCATCCCTACATATACACTGATTCTCCTTCATCTCTACATATATACTCATCCTCCTTCTTCCCTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:87632731..87632840 26863196 MeRIP-seq:(Medium) rs1162643627 Functional Loss SNV dbSNP153 33..33 33 - - - 65725 RMVar_ID_65725 Human_SNP_ID_405777389 m1A Human chr9 + 87633058 87633058 87633058 ATGTAGGGATGAAGGAGGATGAGTATATATGTAAGATGAAGGAAGATGAATATATATGTAGGAAT ATGTAGGGATGAAGGAGGATGAGTATATATGTCAGATGAAGGAAGATGAATATATATGTAGGAAT A C DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:87633030..87633281 26863196 MeRIP-seq:(Medium) rs1019825540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54757,RMVar_hsa_circ_257632,RMVar_hsa_circ_122387,RMVar_hsa_circ_349031,RMVar_hsa_circ_373594,RMVar_hsa_circ_337567,RMVar_hsa_circ_257633,RMVar_hsa_circ_60330,RMVar_hsa_circ_257631,RMVar_hsa_circ_55453,RMVar_hsa_circ_8862,RMVar_hsa_circ_36832 65726 RMVar_ID_65726 Human_SNP_ID_405788495 m1A Human chr9 + 87675402 87675402 87675402 GGGCTGGAGGAAGACAGAGGAATAGGGAGTGCAAGGGGCCGGGTAGTGAAGGGTTGGAGGAGCTC GGGCTGGAGGAAGACAGAGGAATAGGGAGTGCGAGGGGCCGGGTAGTGAAGGGTTGGAGGAGCTC A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:87675389..87675574;chr9:87675394..87675501 26863196 MeRIP-seq:(Medium) rs1178502170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54757,RMVar_hsa_circ_373594,RMVar_hsa_circ_257633,RMVar_hsa_circ_328856,RMVar_hsa_circ_49886,RMVar_hsa_circ_257644,RMVar_hsa_circ_267175,RMVar_hsa_circ_272605,RMVar_hsa_circ_56823,RMVar_hsa_circ_257651,RMVar_hsa_circ_95842,RMVar_hsa_circ_270465,RMVar_hsa_circ_257652 65727 RMVar_ID_65727 Human_SNP_ID_405801342 m1A Human chr9 + 87726252 87726252 87726252 GACAGGGACTGGAAGAGAGGACGCGGTCGAGTAGGTGTGCACCAGCCCTGGCAACGAGAGCGTCT GACAGGGACTGGAAGAGAGGACGCGGTCGAGTGGGTGTGCACCAGCCCTGGCAACGAGAGCGTCT A G CTSL Ensembl:ENSG00000135047 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:87726101..87726350 26863196 MeRIP-seq:(Medium) rs1205671194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184651,Human_RBP_ID_5035737,Human_RBP_ID_5329922,Human_RBP_ID_5534769,Human_RBP_ID_9338940,Human_RBP_ID_9408153,Human_RBP_ID_22466408,Human_RBP_ID_24311531,Human_RBP_ID_26833287 Human_Splice_Rec_1058761,Human_Splice_Rec_1058775,Human_Splice_Rec_1058801,Human_Splice_Rec_1058809,Human_Splice_Rec_1058817 65728 RMVar_ID_65728 Human_SNP_ID_405801764 m1A Human chr9 + 87727713 87727713 87727713 GGCACAGTGGACCAAGTGGAAGGCGATGCACAACAGATTATACGGCATGGTTAGTGAAACTTCCC GGCACAGTGGACCAAGTGGAAGGCGATGCACAGCAGATTATACGGCATGGTTAGTGAAACTTCCC A G CTSL Ensembl:ENSG00000135047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:87727568..87727750 26863196 MeRIP-seq:(Medium) rs1226885290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9408154,Human_RBP_ID_27833152 Human_Splice_Rec_1058763,Human_Splice_Rec_1058789,Human_Splice_Rec_1058811,Human_Splice_Rec_1058819 RMVar_hsa_circ_27132 65729 RMVar_ID_65729 Human_SNP_ID_405801881 m1A Human chr9 - 87728082 87728082 87728082 TGTGTTTCCCTTCCCTGTATTCCTGATTGTGCAGTTCAATCATCTTCATGTTCTTCTCCCACACT TGTGTTTCCCTTCCCTGTATTCCTGATTGTGCGGTTCAATCATCTTCATGTTCTTCTCCCACACT T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:87728004..87728125 26863196 MeRIP-seq:(Medium) rs1249790217 Functional Loss SNV dbSNP153 33..33 33 - - - 65730 RMVar_ID_65730 Human_SNP_ID_405802580 m1A Human chr9 + 87730491 87730491 87730491 CAGAATCAGATAACAATAAATATTGGCTGGTGAAGAACAGGTATAAATTGCCAGAAATACTTACA CAGAATCAGATAACAATAAATATTGGCTGGTGGAGAACAGGTATAAATTGCCAGAAATACTTACA A G CTSL Ensembl:ENSG00000135047 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:87729597..87730490 32194978 MeRIP-seq:(Medium) rs752752549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17666497,Human_RBP_ID_22776480 Human_Splice_Rec_1058773,Human_Splice_Rec_1058785,Human_Splice_Rec_1058799,Human_Splice_Rec_1058807 65731 RMVar_ID_65731 Human_SNP_ID_405871633 m1A Human chr9 - 87974663 87974663 87974663 GCGGGATTAAGCTTGCTGCTGCGTGACAGCGGAGGGCTAGGAAAAGGCGCAGTGGGGCCCGGAGC GCGGGATTAAGCTTGCTGCTGCGTGACAGCGGGGGGCTAGGAAAAGGCGCAGTGGGGCCCGGAGC T C CDK20 Ensembl:ENSG00000156345 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:87974613..87974704 26863196 MeRIP-seq:(Medium) rs1490779333 Functional Loss SNV dbSNP153 33..33 33 - - - 65732 RMVar_ID_65732 Human_SNP_ID_405897010 m1A Human chr9 + 88076875 88076875 88076875 CCGTCTCTCTCTGCCTCCGTCTCCTGCAGCCCAGCTCCGCCTCATTCTCCATTCCTCGCCCAGAA CCGTCTCTCTCTGCCTCCGTCTCCTGCAGCCCGGCTCCGCCTCATTCTCCATTCCTCGCCCAGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:88076785..88076978 26863196 MeRIP-seq:(Medium) rs1157238987 Functional Loss SNV dbSNP153 33..33 33 - - - 65733 RMVar_ID_65733 Human_SNP_ID_405985279 m1A Human chr9 - 88388465 88388465 88388465 CGCCGTCGCTCGTTCGCGCTCCCGCCGGCCCCAGCCTGAGCCAGACGGCGCCTCCCCGCCCCCGC CGCCGTCGCTCGTTCGCGCTCCCGCCGGCCCCGGCCTGAGCCAGACGGCGCCTCCCCGCCCCCGC T C AL353748.3 Ensembl:ENSG00000287769 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:88388426..88388576 26863196 MeRIP-seq:(Medium) rs1417934516 Functional Loss SNV dbSNP153 33..33 33 - - - 65734 RMVar_ID_65734 Human_SNP_ID_405985297 m1A Human chr9 - 88388505 88388494 88388505 TGCTGACCGCCGAGGCTGCAGTCCACAGGCCCACGGGTTCCGCCGTCGCTCGTTCGCGCTCCCGC TGCTGACCGCCGAGGCTGCAGTCCACAGGCCC___________CGTCGCTCGTTCGCGCTCCCGC GGCGGAACCCGT G AL353748.3 Ensembl:ENSG00000287769 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:88388401..88388607 26863196 MeRIP-seq:(Medium) rs1327281384 Functional Loss DEL dbSNP153 33..43 33 - - - 65735 RMVar_ID_65735 Human_SNP_ID_405985610 m1A Human chr9 - 88389135 88389135 88389135 AGGACTGGCCGGTGGGCGTTCCGGCGCCGCGAACCGCGGAGCCTGCAACTTACAAGGTCCGCGGC AGGACTGGCCGGTGGGCGTTCCGGCGCCGCGACCCGCGGAGCCTGCAACTTACAAGGTCCGCGGC T G AL353748.3 Ensembl:ENSG00000287769 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:88389133..88389254 32194978 MeRIP-seq:(Medium) rs924555550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1059001,Human_Splice_Rec_1059003 65736 RMVar_ID_65736 Human_SNP_ID_405988193 m1A Human chr9 - 88396976 88396976 88396976 GACAGCTCCATTCATGGTTCAGTGCCCTACACAGGCATGCCATTTCTCTTTTATACCACATTTCT GACAGCTCCATTCATGGTTCAGTGCCCTACACGGGCATGCCATTTCTCTTTTATACCACATTTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:88396972..88397083 26863196 MeRIP-seq:(Medium) rs1362809420 Functional Loss SNV dbSNP153 33..33 33 - - - 65737 RMVar_ID_65737 Human_SNP_ID_405996428 m1A Human chr9 - 88424679 88424679 88424679 CCAAAACCTTTATTTCAAGTATCTCATACTCAAAACCATCTCTGATCATTCTAGTTTTCTTACAC CCAAAACCTTTATTTCAAGTATCTCATACTCACAACCATCTCTGATCATTCTAGTTTTCTTACAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:88424676..88425236 26863196 MeRIP-seq:(Medium) rs1415618622 Functional Loss SNV dbSNP153 33..33 33 - - - 65738 RMVar_ID_65738 Human_SNP_ID_405996535 m1A Human chr9 - 88425114 88425114 88425114 AACCTCTCCAGAAGGTAAAGTCGTTCTTCAGCAAAGTGCAGTCTACTTTGACCACATGACCCTAC AACCTCTCCAGAAGGTAAAGTCGTTCTTCAGCGAAGTGCAGTCTACTTTGACCACATGACCCTAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:88425112..88425196 26863196 MeRIP-seq:(Medium) rs749333062 Functional Loss SNV dbSNP153 33..33 33 - - - 65739 RMVar_ID_65739 Human_SNP_ID_406008316 m1A Human chr9 - 88467464 88467464 88467464 GCCGGTTCCTTTTGGAGTTCTCCTGACCAACAAGGTAGCCCCACAAATCCCAGTCACATTACCCA GCCGGTTCCTTTTGGAGTTCTCCTGACCAACACGGTAGCCCCACAAATCCCAGTCACATTACCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:88467448..88467613 26863196 MeRIP-seq:(Medium) rs546896459 Functional Loss SNV dbSNP153 33..33 33 - - - 65740 RMVar_ID_65740 Human_SNP_ID_406025777 m1A Human chr9 + 88534297 88534297 88534297 AAGAGCACGGTGTGGGGGAAGCGCAGGAGGCAATAGGTGGGGCGGGACGGAGGGCAGGGCGCTGC AAGAGCACGGTGTGGGGGAAGCGCAGGAGGCACTAGGTGGGGCGGGACGGAGGGCAGGGCGCTGC A C NXNL2 Ensembl:ENSG00000130045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:88533947..88534593 26863196 MeRIP-seq:(Medium) rs1429409689 Functional Loss SNV dbSNP153 33..33 33 - - - 65741 RMVar_ID_65741 Human_SNP_ID_406025797 m1A Human chr9 + 88534336 88534336 88534336 GGGCGGGACGGAGGGCAGGGCGCTGCGTCGGGAGAAAGTGTAGAAGCGCTGGGGAGAGTGCCCAC GGGCGGGACGGAGGGCAGGGCGCTGCGTCGGGCGAAAGTGTAGAAGCGCTGGGGAGAGTGCCCAC A C NXNL2 Ensembl:ENSG00000130045 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:88533913..88534572 26863196 MeRIP-seq:(Medium) rs1234739903 Functional Loss SNV dbSNP153 33..33 33 - - - 65742 RMVar_ID_65742 Human_SNP_ID_406025870 m1A Human chr9 - 88534498 88534497 88534498 CTGCGCCCCGCTCACACTCCCGCACCCTCCCCACACTGCGCCCTGCCCACACTCCTGCACTCTCT CTGCGCCCCGCTCACACTCCCGCACCCTCCCC_CACTGCGCCCTGCCCACACTCCTGCACTCTCT GT G lnc-SHC3-10,lnc-SHC3-10:2,lnc-SHC3-10:3 RNACentral:URS0000D570E3,RNACentral:URS0000D59A47,RNACentral:URS0000D56CF8 lincRNA,lincRNA,lincRNA intron,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:88534447..88534574 26863196 MeRIP-seq:(Medium) rs1164501717 Functional Loss DEL dbSNP153 33..33 33 - - - 65743 RMVar_ID_65743 Human_SNP_ID_406025871 m1A Human chr9 - 88534498 88534498 88534498 CTGCGCCCCGCTCACACTCCCGCACCCTCCCCACACTGCGCCCTGCCCACACTCCTGCACTCTCT CTGCGCCCCGCTCACACTCCCGCACCCTCCCCCCACTGCGCCCTGCCCACACTCCTGCACTCTCT T G lnc-SHC3-10,lnc-SHC3-10:2,lnc-SHC3-10:3 RNACentral:URS0000D570E3,RNACentral:URS0000D59A47,RNACentral:URS0000D56CF8 lincRNA,lincRNA,lincRNA intron,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:88534447..88534574 26863196 MeRIP-seq:(Medium) rs1367154857 Functional Loss SNV dbSNP153 33..33 33 - - - 65744 RMVar_ID_65744 Human_SNP_ID_406025985 m1A Human chr9 + 88534735 88534735 88534735 GCGCAGTGAGGGGAAACTGTGGAATGTGGGCGAGGCGCAGTTGGAGAAGAGTGCGGGGATGTGGG GCGCAGTGAGGGGAAACTGTGGAATGTGGGCGGGGCGCAGTTGGAGAAGAGTGCGGGGATGTGGG A G NXNL2 Ensembl:ENSG00000130045 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:88534708..88534785 26863196 MeRIP-seq:(Medium) rs1471895995 Functional Loss SNV dbSNP153 33..33 33 - - - 65745 RMVar_ID_65745 Human_SNP_ID_406026231 m1A Human chr9 - 88535230 88535230 88535230 TGGAGCAATTGTGTTCGCGCCGACAATGAGACACTCAGACACCAGAGACCCCAGATACCTGGGCG TGGAGCAATTGTGTTCGCGCCGACAATGAGACCCTCAGACACCAGAGACCCCAGATACCTGGGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:88535131..88535279 26863196 MeRIP-seq:(Medium) rs1386755565 Functional Loss SNV dbSNP153 33..33 33 - - - 65746 RMVar_ID_65746 Human_SNP_ID_406026417 m1A Human chr9 + 88535631 88535631 88535631 GGTGGCCGAGGCGCGGCGGCCCGCGCCCTTCGAAGTGGTCTTCGTGTCAGCCGACGGCAGCTCCC GGTGGCCGAGGCGCGGCGGCCCGCGCCCTTCGCAGTGGTCTTCGTGTCAGCCGACGGCAGCTCCC A C NXNL2 Ensembl:ENSG00000130045 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:88535591..88535676 26863410 MeRIP-seq:(Medium) rs141815425 Functional Loss SNV dbSNP153 33..33 33 - - - 65747 RMVar_ID_65747 Human_SNP_ID_406138883 m1A Human chr9 - 88991528 88991528 88991528 CGGGCCTGGGGTCCTGCTCGGTCGCGTCCTGCAGCCGCCTTCTGGTCCCTGAGTCCCTGTTGCCC CGGGCCTGGGGTCCTGCTCGGTCGCGTCCTGCGGCCGCCTTCTGGTCCCTGAGTCCCTGTTGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:88991478..88991644 26863196 MeRIP-seq:(Medium) rs200244462 Functional Loss SNV dbSNP153 33..33 33 - - - 65748 RMVar_ID_65748 Human_SNP_ID_406141264 m1A Human chr9 - 89001162 89001162 89001162 GCATTCACAGACGATTAGCTCCAAAATCCACGAGAGGGCGCCCCAGGAACATTCATTTCAAAGGG GCATTCACAGACGATTAGCTCCAAAATCCACGCGAGGGCGCCCCAGGAACATTCATTTCAAAGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89001111..89001215 26863196 MeRIP-seq:(Medium) rs746085419 Functional Loss SNV dbSNP153 33..33 33 - - - 65749 RMVar_ID_65749 Human_SNP_ID_406213244 m1A Human chr9 - 89310431 89310431 89310431 GGCCCGGAGCCGGCGCGGTGGCGGCGGGCGCCAGTGGTCCCAGCCACTCGGGAGGCCGAGGTGGA GGCCCGGAGCCGGCGCGGTGGCGGCGGGCGCCTGTGGTCCCAGCCACTCGGGAGGCCGAGGTGGA T A lnc-SEMA4D-4,lnc-SEMA4D-4:2 RNACentral:URS00008C1FF3,RNACentral:URS0000D59E0D lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89310392..89310520 26863196 MeRIP-seq:(Medium) rs1291957390 Functional Loss SNV dbSNP153 33..33 33 - - - 65750 RMVar_ID_65750 Human_SNP_ID_406213245 m1A Human chr9 - 89310431 89310431 89310431 GGCCCGGAGCCGGCGCGGTGGCGGCGGGCGCCAGTGGTCCCAGCCACTCGGGAGGCCGAGGTGGA GGCCCGGAGCCGGCGCGGTGGCGGCGGGCGCCGGTGGTCCCAGCCACTCGGGAGGCCGAGGTGGA T C lnc-SEMA4D-4,lnc-SEMA4D-4:2 RNACentral:URS00008C1FF3,RNACentral:URS0000D59E0D lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89310392..89310520 26863196 MeRIP-seq:(Medium) rs1291957390 Functional Loss SNV dbSNP153 33..33 33 - - - 65751 RMVar_ID_65751 Human_SNP_ID_406213249 m1A Human chr9 - 89310456 89310445 89310456 GCCTGCGGAGCCACGCGTAGAGAGAGGCCCGGAGCCGGCGCGGTGGCGGCGGGCGCCAGTGGTCC GCCTGCGGAGCCACGCGTAGAGAGAGGCCCGG___________TGGCGGCGGGCGCCAGTGGTCC ACCGCGCCGGCT A lnc-SEMA4D-4,lnc-SEMA4D-4:2 RNACentral:URS00008C1FF3,RNACentral:URS0000D59E0D lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:89310412..89310549 26863196 MeRIP-seq:(Medium) rs1425982235 Functional Loss DEL dbSNP153 33..43 33 - - - 65752 RMVar_ID_65752 Human_SNP_ID_406213628 m1A Human chr9 - 89311224 89311224 89311224 GAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGCCCAGGCAACAACTCGCCGGAGACTAACGAC GAAGAGCGGGCGCAGCAGACAAAACCACGTCCTGCCCAGGCAACAACTCGCCGGAGACTAACGAC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:89311201..89311225 26863196 MeRIP-seq:(Medium) rs1028272809 Functional Loss SNV dbSNP153 33..33 33 - - - 65753 RMVar_ID_65753 Human_SNP_ID_406213629 m1A Human chr9 - 89311224 89311224 89311224 GAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGCCCAGGCAACAACTCGCCGGAGACTAACGAC GAAGAGCGGGCGCAGCAGACAAAACCACGTCCGGCCCAGGCAACAACTCGCCGGAGACTAACGAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:89311201..89311225 26863196 MeRIP-seq:(Medium) rs1028272809 Functional Loss SNV dbSNP153 33..33 33 - - - 65754 RMVar_ID_65754 Human_SNP_ID_406213630 m1A Human chr9 - 89311224 89311224 89311224 GAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGCCCAGGCAACAACTCGCCGGAGACTAACGAC GAAGAGCGGGCGCAGCAGACAAAACCACGTCCCGCCCAGGCAACAACTCGCCGGAGACTAACGAC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:89311201..89311225 26863196 MeRIP-seq:(Medium) rs1028272809 Functional Loss SNV dbSNP153 33..33 33 - - - 65755 RMVar_ID_65755 Human_SNP_ID_406213663 m1A Human chr9 - 89311252 89311252 89311252 CGCGCTGCAGAAAATGAAACGAGAGCGCGAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGCCC CGCGCTGCAGAAAATGAAACGAGAGCGCGAAGGGCGGGCGCAGCAGACAAAACCACGTCCAGCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:89311201..89311564;chr9:89311201..89311392;chr9:89311201..89311300 26863196 MeRIP-seq:(Medium) rs759966109 Functional Loss SNV dbSNP153 33..33 33 - - - 65756 RMVar_ID_65756 Human_SNP_ID_406213665 m1A Human chr9 - 89311254 89311254 89311254 GGCGCGCTGCAGAAAATGAAACGAGAGCGCGAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGC GGCGCGCTGCAGAAAATGAAACGAGAGCGCGAGGAGCGGGCGCAGCAGACAAAACCACGTCCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:89311201..89311402 26863196 MeRIP-seq:(Medium) rs1203736953 Functional Loss SNV dbSNP153 33..33 33 - - - 65757 RMVar_ID_65757 Human_SNP_ID_406213698 m1A Human chr9 + 89311303 89311303 89311303 TTTTCTGCAGCGCGCCAGCAGGATGGCCCACAAGCAGATCTACTACTCGGACAAGTACTTCGACG TTTTCTGCAGCGCGCCAGCAGGATGGCCCACAGGCAGATCTACTACTCGGACAAGTACTTCGACG A G CKS2 Ensembl:ENSG00000123975 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:89311252..89311650 26863196 MeRIP-seq:(Medium) rs761873716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_721618,Human_RBP_ID_1059870,Human_RBP_ID_1706859,Human_RBP_ID_2066461,Human_RBP_ID_3904259,Human_RBP_ID_5033585,Human_RBP_ID_5482480,Human_RBP_ID_5634255,Human_RBP_ID_7944451,Human_RBP_ID_8275277,Human_RBP_ID_8707659,Human_RBP_ID_9338944,Human_RBP_ID_16727908,Human_RBP_ID_17322642,Human_RBP_ID_17437097,Human_RBP_ID_18542471,Human_RBP_ID_18911215,Human_RBP_ID_19143493,Human_RBP_ID_22118731,Human_RBP_ID_22518531,Human_RBP_ID_23117215,Human_RBP_ID_26360382,Human_RBP_ID_27547120 Human_Splice_Rec_1059219 RMVar_hsa_circ_97365,RMVar_hsa_circ_257701 65758 RMVar_ID_65758 Human_SNP_ID_406214771 m1A Human chr9 + 89315296 89315296 89315296 CTAGGCTGGGTTCATTACATGATTCATGAGCCAGGTAAGCTATGCTATGTTATAGTAAAGCAGTA CTAGGCTGGGTTCATTACATGATTCATGAGCCGGGTAAGCTATGCTATGTTATAGTAAAGCAGTA A G CKS2 Ensembl:ENSG00000123975 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:89315176..89315300 32194978 MeRIP-seq:(Medium) rs754503421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961417,Human_RBP_ID_1706872,Human_RBP_ID_5407775,Human_RBP_ID_18140515,Human_RBP_ID_26739759 Human_Splice_Rec_1059221 RMVar_hsa_circ_30075,RMVar_hsa_circ_97365,RMVar_hsa_circ_107557,RMVar_hsa_circ_257701,RMVar_hsa_circ_257702 65759 RMVar_ID_65759 Human_SNP_ID_406217267 m1A Human chr9 + 89323366 89323364 89323367 TCTGACCCAGAATGTGTCAGATGGGTGAGATAAGGAGGGTGTAGAGGAGACTGCACTAGGGAAAG TCTGACCCAGAATGTGTCAGATGGGTGAGAT___GAGGGTGTAGAGGAGACTGCACTAGGGAAAG TAAG T SECISBP2 Ensembl:ENSG00000187742 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:89323319..89323526 26863196 MeRIP-seq:(Medium) rs1023412480 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_7944573,Human_RBP_ID_16728430,Human_RBP_ID_17177029,Human_RBP_ID_24317409 RMVar_hsa_circ_43490,RMVar_hsa_circ_355698,RMVar_hsa_circ_377703,RMVar_hsa_circ_66762,RMVar_hsa_circ_257703,RMVar_hsa_circ_6873,RMVar_hsa_circ_257704 65760 RMVar_ID_65760 Human_SNP_ID_406217279 m1A Human chr9 - 89323408 89323402 89323408 TCGCCTGGCTCTCACCTGCCCTCCAAGGCTCTATCTCTGTCTCTTTCCCTAGTGCAGTCTCCTCT TCGCCTGGCTCTCACCTGCCCTCCAAGGCTCT______GTCTCTTTCCCTAGTGCAGTCTCCTCT CAGAGAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89323251..89323722 26863196 MeRIP-seq:(Medium) rs1481846452 Functional Loss DEL dbSNP153 33..38 33 - - - 65761 RMVar_ID_65761 Human_SNP_ID_406217283 m1A Human chr9 - 89323408 89323408 89323408 TCGCCTGGCTCTCACCTGCCCTCCAAGGCTCTATCTCTGTCTCTTTCCCTAGTGCAGTCTCCTCT TCGCCTGGCTCTCACCTGCCCTCCAAGGCTCTGTCTCTGTCTCTTTCCCTAGTGCAGTCTCCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89323251..89323722 26863196 MeRIP-seq:(Medium) rs1453125947 Functional Loss SNV dbSNP153 33..33 33 - - - 65762 RMVar_ID_65762 Human_SNP_ID_406230436 m1A Human chr9 + 89370545 89370543 89370545 GCTGGCATGTGGTGTGTGTGGCATGTGGTGTGAGGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC GCTGGCATGTGGTGTGTGTGGCATGTGGTGT__GGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC TGA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:89370506..89370614 26863196 MeRIP-seq:(Medium) rs751026735 Functional Loss DEL dbSNP153 32..33 33 - - - 65763 RMVar_ID_65763 Human_SNP_ID_406230437 m1A Human chr9 + 89370545 89370544 89370545 GCTGGCATGTGGTGTGTGTGGCATGTGGTGTGAGGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC GCTGGCATGTGGTGTGTGTGGCATGTGGTGTG_GGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:89370506..89370614 26863196 MeRIP-seq:(Medium) rs142089755 Functional Loss DEL dbSNP153 33..33 33 - - - 65764 RMVar_ID_65764 Human_SNP_ID_406230440 m1A Human chr9 + 89370545 89370545 89370545 GCTGGCATGTGGTGTGTGTGGCATGTGGTGTGAGGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC GCTGGCATGTGGTGTGTGTGGCATGTGGTGTGTGGGGGTGTGGTGCTGGTGTGTGGTATGTCTGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:89370506..89370614 26863196 MeRIP-seq:(Medium) rs949662681 Functional Loss SNV dbSNP153 33..33 33 - - - 65765 RMVar_ID_65765 Human_SNP_ID_406240571 m1A Human chr9 - 89404565 89404518 89404566 ACGGGATGGGGACTCCACTTCCTGGGATGCTGAGGCGGGTGGCTGGGGACGGGACAGGAACTCCA ACGGGATGGGGACTCCACTTCCTGGGATGCT__________________________________ GAGCATCCCAGGAAGTGGAGTTCCTGTCCCGTCCCCAGCCACCCGCCTC G SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:89404555..89404684 26863196 MeRIP-seq:(Medium) rs71358576 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716,RMVar_hsa_circ_49356,RMVar_hsa_circ_257722,RMVar_hsa_circ_39393,RMVar_hsa_circ_378120 65766 RMVar_ID_65766 Human_SNP_ID_406240637 m1A Human chr9 - 89404648 89404648 89404648 CCCACTTCCTGGGATGCTGAGGTGAGTGGCTGAGGTCGGGATGGGGACTCCACTTCCTGGGATGC CCCACTTCCTGGGATGCTGAGGTGAGTGGCTGGGGTCGGGATGGGGACTCCACTTCCTGGGATGC T C SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89404597..89404698 26863196 MeRIP-seq:(Medium) rs13286884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716,RMVar_hsa_circ_49356,RMVar_hsa_circ_257722,RMVar_hsa_circ_39393,RMVar_hsa_circ_378120 65767 RMVar_ID_65767 Human_SNP_ID_406240640 m1A Human chr9 - 89404661 89404661 89404661 ACGGGATGGGGACCCCACTTCCTGGGATGCTGAGGTGAGTGGCTGAGGTCGGGATGGGGACTCCA ACGGGATGGGGACCCCACTTCCTGGGATGCTGCGGTGAGTGGCTGAGGTCGGGATGGGGACTCCA T G SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:89404615..89404704 26863196 MeRIP-seq:(Medium) rs1439281537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716,RMVar_hsa_circ_49356,RMVar_hsa_circ_257722,RMVar_hsa_circ_39393,RMVar_hsa_circ_378120 65768 RMVar_ID_65768 Human_SNP_ID_406251780 m1A Human chr9 - 89447048 89447048 89447048 GGTTCGGACTGGCTGCTGGGCTGCGGTGGGAGAGATGGTCTGGGCCTGGGAGATGAGATGGACAG GGTTCGGACTGGCTGCTGGGCTGCGGTGGGAGGGATGGTCTGGGCCTGGGAGATGAGATGGACAG T C SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89446998..89447124 26863196 MeRIP-seq:(Medium) rs1467131467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716 65769 RMVar_ID_65769 Human_SNP_ID_406264279 m1A Human chr9 + 89492772 89492772 89492772 TTCGCAGAACACCTGCAATCAGCCTGCCTCCCACCCGAGGAGACTGCCCGAGCTCCTGCAAGGCC TTCGCAGAACACCTGCAATCAGCCTGCCTCCCTCCCGAGGAGACTGCCCGAGCTCCTGCAAGGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89492770..89492869 26863196 MeRIP-seq:(Medium) rs1412438604 Functional Loss SNV dbSNP153 33..33 33 - - - 65770 RMVar_ID_65770 Human_SNP_ID_406265546 m1A Human chr9 + 89498008 89497999 89498009 ATGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGAGGCGGCCGGGCCGGGGAGGGGGTGGCGGGGAG ATGGCGGCGGCGGCGGCGGCGGCA__________GCGGCCGGGCCGGGGAGGGGGTGGCGGGGAG AGCGGCGGGAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89497913..89498095 26863196 MeRIP-seq:(Medium) rs1323209212 Functional Loss DEL dbSNP153 25..34 33 - - - 65771 RMVar_ID_65771 Human_SNP_ID_406265547 m1A Human chr9 + 89497999 89497999 89497999 GCGCCAGGAATGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGAGGCGGCCGGGCCGGGGAGGGGGT GCGCCAGGAATGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGGCGGCCGGGCCGGGGAGGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr9:89497953..89498089;chr9:89497913..89498062 26863196 MeRIP-seq:(Medium) rs1368804297 Functional Loss SNV dbSNP153 33..33 33 - - - 65772 RMVar_ID_65772 Human_SNP_ID_406265550 m1A Human chr9 + 89498008 89498008 89498008 ATGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGAGGCGGCCGGGCCGGGGAGGGGGTGGCGGGGAG ATGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGGCGGCCGGGCCGGGGAGGGGGTGGCGGGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:89497913..89498095 26863196 MeRIP-seq:(Medium) rs947979611 Functional Loss SNV dbSNP153 33..33 33 - - - 65773 RMVar_ID_65773 Human_SNP_ID_226764997 m1A Human chr5 - 31401459 31401459 31401459 AGGTGGGAAAGAGAGCATCAAGAGAGAGAGCCAGATGAGACTGAAGACATCAAGAAATAAAGGAG AGGTGGGAAAGAGAGCATCAAGAGAGAGAGCCGGATGAGACTGAAGACATCAAGAAATAAAGGAG T C DROSHA Ensembl:ENSG00000113360 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:31401411..31401579 26863196 MeRIP-seq:(Medium) rs559000514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77548,Human_RBP_ID_3967803,Human_RBP_ID_8236776,Human_RBP_ID_15420242,Human_RBP_ID_17662372,Human_RBP_ID_18537922,Human_RBP_ID_24102597,Human_RBP_ID_24385465,Human_RBP_ID_26350692,Human_RBP_ID_27825255 Human_miRNA_ID_337793 65774 RMVar_ID_65774 Human_SNP_ID_226773582 m1A Human chr5 + 31439981 31439981 31439981 AAATCTCTCTGACACCAACCCACATCTCCCCAAATAATTCAACAGCTGCCTGTCGAGTCTCAACC AAATCTCTCTGACACCAACCCACATCTCCCCACATAATTCAACAGCTGCCTGTCGAGTCTCAACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:31439979..31440159 26863196 MeRIP-seq:(Medium) rs1202443777 Functional Loss SNV dbSNP153 33..33 33 - - - 65775 RMVar_ID_65775 Human_SNP_ID_226790640 m1A Human chr5 - 31515112 31515112 31515112 TGGCAAAGACAAGAACTATACCTCAATCAAGGAAAAAGAGCCCGAGGAGACCATGCCTGACAAGA TGGCAAAGACAAGAACTATACCTCAATCAAGGGAAAAGAGCCCGAGGAGACCATGCCTGACAAGA T C DROSHA Ensembl:ENSG00000113360 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:31514960..31515169 26863196 MeRIP-seq:(Medium) rs997346858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947123,Human_RBP_ID_2924426,Human_RBP_ID_3967138,Human_RBP_ID_17300040,Human_RBP_ID_18537926,Human_RBP_ID_22099329,Human_RBP_ID_26352023,Human_RBP_ID_27825259 Human_miRNA_ID_2579567 RMVar_hsa_circ_101864,RMVar_hsa_circ_230606,RMVar_hsa_circ_106761,RMVar_hsa_circ_230621,RMVar_hsa_circ_99921,RMVar_hsa_circ_2478,RMVar_hsa_circ_230629,RMVar_hsa_circ_102642,RMVar_hsa_circ_230633,RMVar_hsa_circ_268220,RMVar_hsa_circ_327275,RMVar_hsa_circ_51874,RMVar_hsa_circ_110996,RMVar_hsa_circ_230645,RMVar_hsa_circ_230648,RMVar_hsa_circ_33991,RMVar_hsa_circ_338101,RMVar_hsa_circ_371533,RMVar_hsa_circ_319866,RMVar_hsa_circ_356509,RMVar_hsa_circ_27410,RMVar_hsa_circ_25963 65776 RMVar_ID_65776 Human_SNP_ID_226793180 m1A Human chr5 + 31526426 31526426 31526426 GGAGGTGGGAAGTTGTGGTGAGAATAGCCCGGAGGGTACTGATAATTAACCTGCTGCGGCATGAC GGAGGTGGGAAGTTGTGGTGAGAATAGCCCGGGGGGTACTGATAATTAACCTGCTGCGGCATGAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:31526376..31526425 26863196 MeRIP-seq:(Medium) rs749291437 Functional Loss SNV dbSNP153 33..33 33 - - - 65777 RMVar_ID_65777 Human_SNP_ID_226793296 m1A Human chr5 + 31526699 31526699 31526699 GCTGACGGAGGCATGGGTGGGGGGAAGGGTACAAAGTCTGGTCGTGGAGGGAGAAAATTGGGGGC GCTGACGGAGGCATGGGTGGGGGGAAGGGTACGAAGTCTGGTCGTGGAGGGAGAAAATTGGGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:31526278..31526900 26863196 MeRIP-seq:(Medium) rs1451508849 Functional Loss SNV dbSNP153 33..33 33 - - - 65778 RMVar_ID_65778 Human_SNP_ID_226820926 m1A Human chr5 + 31639259 31639259 31639259 GCAGGCAGCCGAGGAGCCGCAGGCCGAACCCAAGGCACCGGGATTGCGCCTCCCGCGGCTGCCGG GCAGGCAGCCGAGGAGCCGCAGGCCGAACCCAGGGCACCGGGATTGCGCCTCCCGCGGCTGCCGG A G PDZD2 Ensembl:ENSG00000133401 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:31639167..31639259 26863410 MeRIP-seq:(Medium) rs976504253 Functional Loss SNV dbSNP153 33..33 33 - - - 65779 RMVar_ID_65779 Human_SNP_ID_226941062 m1A Human chr5 - 32109409 32109409 32109409 AAGCAGCTCATGCCACCAGAGGAGGAGTGGCCAGAGTGAGTTTCCCAAGTAGCGTGAGTCACGAC AAGCAGCTCATGCCACCAGAGGAGGAGTGGCCGGAGTGAGTTTCCCAAGTAGCGTGAGTCACGAC T C AC025178.2 Ensembl:ENSG00000250764 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32109364..32109435 26863196 MeRIP-seq:(Medium) rs999936268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612160 65780 RMVar_ID_65780 Human_SNP_ID_226945451 m1A Human chr5 + 32126208 32126207 32126209 CTTGAGAGAAAGGAGAATGGTTCACCCCGAGCAGAGTTACTTGGTGAACGCCGCCACCACCGCCC CTTGAGAGAAAGGAGAATGGTTCACCCCGAGC__AGTTACTTGGTGAACGCCGCCACCACCGCCC CAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:32126157..32126322 26863196 MeRIP-seq:(Medium) rs778418168 Functional Loss DEL dbSNP153 33..34 33 - - - 65781 RMVar_ID_65781 Human_SNP_ID_226945469 m1A Human chr5 - 32126259 32126259 32126259 ACTTAGACCCTGAAGTGGAATGTCTGAAGGCCAACACCAATGAGGTTCTGTGGGCGGTGGTGGCG ACTTAGACCCTGAAGTGGAATGTCTGAAGGCCGACACCAATGAGGTTCTGTGGGCGGTGGTGGCG T C GOLPH3 Ensembl:ENSG00000113384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32126212..32126364 26863196 MeRIP-seq:(Medium) rs764919742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641062,Human_RBP_ID_1653285,Human_RBP_ID_1994281,Human_RBP_ID_3768061,Human_RBP_ID_8613730,Human_RBP_ID_8889303,Human_RBP_ID_15423592,Human_RBP_ID_18046987,Human_RBP_ID_18841236,Human_RBP_ID_22512293,Human_RBP_ID_27336249 RMVar_hsa_circ_109686,RMVar_hsa_circ_121061,RMVar_hsa_circ_230663,RMVar_hsa_circ_119773,RMVar_hsa_circ_230665,RMVar_hsa_circ_230666,RMVar_hsa_circ_230664 65782 RMVar_ID_65782 Human_SNP_ID_226950399 m1A Human chr5 + 32143852 32143852 32143852 CAATTAACATACAGCCACGTAATCCAGATGATATACAGTCATTCCAAAATGATGTGTAACCCTAT CAATTAACATACAGCCACGTAATCCAGATGATGTACAGTCATTCCAAAATGATGTGTAACCCTAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:32143801..32143900 32194978 MeRIP-seq:(Medium) rs747637818 Functional Loss SNV dbSNP153 33..33 33 - - - 65783 RMVar_ID_65783 Human_SNP_ID_226954360 m1A Human chr5 + 32158223 32158223 32158223 CTACTCAGAGCTCTTACCACTCTCCATATCAGATATTTCAAAACCCCATTCTCCCCAAACCTCTA CTACTCAGAGCTCTTACCACTCTCCATATCAGGTATTTCAAAACCCCATTCTCCCCAAACCTCTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:32158220..32158703 26863196 MeRIP-seq:(Medium) rs1458257697 Functional Loss SNV dbSNP153 33..33 33 - - - 65784 RMVar_ID_65784 Human_SNP_ID_226954435 m1A Human chr5 - 32158585 32158585 32158585 GGGGGATTGTGGAGCCAGCAGGAGGAAGAGTGAGGAGTAGTGGAGATGGACTTGCTGATGATACC GGGGGATTGTGGAGCCAGCAGGAGGAAGAGTGGGGAGTAGTGGAGATGGACTTGCTGATGATACC T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32158583..32158663 26863196 MeRIP-seq:(Medium) rs1284128384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12267,Human_RBP_ID_839247,Human_RBP_ID_5655620,Human_RBP_ID_7428795,Human_RBP_ID_15424573,Human_RBP_ID_17069700,Human_RBP_ID_17159473,Human_RBP_ID_18056723,Human_RBP_ID_24103091 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 65785 RMVar_ID_65785 Human_SNP_ID_226958768 m1A Human chr5 - 32173895 32173895 32173895 CGAGGACGACGCGCAGAGCCGCCGCGACGAGCAGGACGACGACGACAAGGGCGACTCCAAGGAAA CGAGGACGACGCGCAGAGCCGCCGCGACGAGCTGGACGACGACGACAAGGGCGACTCCAAGGAAA T A GOLPH3 Ensembl:ENSG00000113384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32173845..32174325 26863196 MeRIP-seq:(Medium) rs772604415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249949,Human_RBP_ID_840152,Human_RBP_ID_9399001,Human_RBP_ID_23050104,Human_RBP_ID_23116239 Human_Splice_Rec_640589,Human_Splice_Rec_640601 Human_miRNA_ID_1967688 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666 65786 RMVar_ID_65786 Human_SNP_ID_226958769 m1A Human chr5 - 32173895 32173895 32173895 CGAGGACGACGCGCAGAGCCGCCGCGACGAGCAGGACGACGACGACAAGGGCGACTCCAAGGAAA CGAGGACGACGCGCAGAGCCGCCGCGACGAGCGGGACGACGACGACAAGGGCGACTCCAAGGAAA T C GOLPH3 Ensembl:ENSG00000113384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32173845..32174325 26863196 MeRIP-seq:(Medium) rs772604415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249949,Human_RBP_ID_840152,Human_RBP_ID_9399001,Human_RBP_ID_23050104,Human_RBP_ID_23116239 Human_Splice_Rec_640589,Human_Splice_Rec_640601 Human_miRNA_ID_1967688 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666 65787 RMVar_ID_65787 Human_SNP_ID_226958918 m1A Human chr5 - 32174247 32174247 32174247 GGGGTGTTTCGGGGACTGCGGCCACAGGCAGGAAGGCGCTCCTCTCCTGCCCCGCCGACGCCCGG GGGGTGTTTCGGGGACTGCGGCCACAGGCAGGGAGGCGCTCCTCTCCTGCCCCGCCGACGCCCGG T C GOLPH3 Ensembl:ENSG00000113384 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:32173892..32174325 26863196 MeRIP-seq:(Medium) rs1197835057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1321273,Human_RBP_ID_4845643,Human_RBP_ID_5427285,Human_RBP_ID_5509555,Human_RBP_ID_9335191,Human_RBP_ID_22099340 Human_miRNA_ID_2442834,Human_miRNA_ID_3021296 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666 65788 RMVar_ID_65788 Human_SNP_ID_226958928 m1A Human chr5 + 32174263 32174263 32174263 CAGGAGAGGAGCGCCTTCCTGCCTGTGGCCGCAGTCCCCGAAACACCCCGAGCTCCAAGGCGGAG CAGGAGAGGAGCGCCTTCCTGCCTGTGGCCGCGGTCCCCGAAACACCCCGAGCTCCAAGGCGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:32173769..32174375;chr5:32173826..32174421 26863196 MeRIP-seq:(Medium) rs1255074633 Functional Loss SNV dbSNP153 33..33 33 - - - 65789 RMVar_ID_65789 Human_SNP_ID_226958937 m1A Human chr5 - 32174284 32174284 32174284 TTGGAAAGGCGCCGCCGCCGCCTCCGCCTTGGAGCTCGGGGTGTTTCGGGGACTGCGGCCACAGG TTGGAAAGGCGCCGCCGCCGCCTCCGCCTTGGCGCTCGGGGTGTTTCGGGGACTGCGGCCACAGG T G GOLPH3 Ensembl:ENSG00000113384 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:32174187..32174288 26863410 MeRIP-seq:(Medium) rs951287696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845643,Human_RBP_ID_9335191 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666 65790 RMVar_ID_65790 Human_SNP_ID_226959052 m1A Human chr5 - 32174518 32174518 32174518 TAGTGAAGGGGAAACGGGGAACGGAAGGAGGGAGGGCACGTCACGGGAGCAGGACTGCAGGACCG TAGTGAAGGGGAAACGGGGAACGGAAGGAGGGTGGGCACGTCACGGGAGCAGGACTGCAGGACCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32174470..32174659 26863196 MeRIP-seq:(Medium) rs1273161618 Functional Loss SNV dbSNP153 33..33 33 - - - 65791 RMVar_ID_65791 Human_SNP_ID_226988674 m1A Human chr5 - 32293987 32293987 32293987 AATGGATAGACGTGGGCAATATGGAGCAGAGCACAGGCTGTGAGAGGCAGGGAGTAGGTAAGAGT AATGGATAGACGTGGGCAATATGGAGCAGAGCTCAGGCTGTGAGAGGCAGGGAGTAGGTAAGAGT T A MTMR12 Ensembl:ENSG00000150712 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:32293982..32294216 26863196 MeRIP-seq:(Medium) rs1157031526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839264 RMVar_hsa_circ_116884,RMVar_hsa_circ_230689 65792 RMVar_ID_65792 Human_SNP_ID_226993063 m1A Human chr5 + 32311647 32311647 32311647 AAGAAGGCTTCTCATTAGGCATTTGGATTAAGAACTATTGCTCAAGAAGCCCTGAGCAAGGCCTA AAGAAGGCTTCTCATTAGGCATTTGGATTAAGGACTATTGCTCAAGAAGCCCTGAGCAAGGCCTA A G RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:32311645..32311787 32194978 MeRIP-seq:(Medium) rs1055619606 Functional Loss SNV dbSNP153 33..33 33 - - - 65793 RMVar_ID_65793 Human_SNP_ID_226993334 m1A Human chr5 - 32312611 32312611 32312611 GGCGACGGGGCAGCCAGGCGGGCTGAGGCCGCAGGAGCGCGCTGGGGCCTCCGCGCGGGCCGGAA GGCGACGGGGCAGCCAGGCGGGCTGAGGCCGCGGGAGCGCGCTGGGGCCTCCGCGCGGGCCGGAA T C MTMR12 Ensembl:ENSG00000150712 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:32312512..32312641 26863196 MeRIP-seq:(Medium) rs1433601490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1069478,Human_RBP_ID_5242467 RMVar_hsa_circ_116884,RMVar_hsa_circ_230689 65794 RMVar_ID_65794 Human_SNP_ID_226993418 m1A Human chr5 - 32312798 32312798 32312798 GAAAGGAGTAGTCGGCGGTGGCGGCGGCACCAAGGCCCCCAAGCCCTCCTTCGTGTCGTACGTAC GAAAGGAGTAGTCGGCGGTGGCGGCGGCACCAGGGCCCCCAAGCCCTCCTTCGTGTCGTACGTAC T C MTMR12 Ensembl:ENSG00000150712 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32312765..32312930 26863196 MeRIP-seq:(Medium) rs1488625235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845140,Human_RBP_ID_8893488 Human_Splice_Rec_640605,Human_Splice_Rec_640633,Human_Splice_Rec_640663,Human_Splice_Rec_640699,Human_Splice_Rec_640707 RMVar_hsa_circ_116884,RMVar_hsa_circ_230689 65795 RMVar_ID_65795 Human_SNP_ID_227013311 m1A Human chr5 + 32390278 32390278 32390278 CCCCTTGTATCACCAACGTGGACACTCACTGCAGGCCCCTGAGGCTGAGGAGGCATGCCTGGTCG CCCCTTGTATCACCAACGTGGACACTCACTGCCGGCCCCTGAGGCTGAGGAGGCATGCCTGGTCG A C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:32390276..32390425 32194978 MeRIP-seq:(Medium) rs774496675 Functional Loss SNV dbSNP153 33..33 33 - - - 65796 RMVar_ID_65796 Human_SNP_ID_227020951 m1A Human chr5 + 32417609 32417609 32417609 TCTTCATTAAACGCAGTAAGTCATATACTTCAATAGTTTACAAAGAAACTCTGTAGGTTAAGAAA TCTTCATTAAACGCAGTAAGTCATATACTTCAGTAGTTTACAAAGAAACTCTGTAGGTTAAGAAA A G RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:32417607..32417718 26863196 MeRIP-seq:(Medium) rs1479044355 Functional Loss SNV dbSNP153 33..33 33 - - - 65797 RMVar_ID_65797 Human_SNP_ID_227025981 m1A Human chr5 + 32436327 32436322 32436327 CCCACCACCACGCCCGGCTGATTTTTTTTTTTATTTTTAGTAGACACGTGGTTTCACCGTGTTAG CCCACCACCACGCCCGGCTGATTTTTTT_____TTTTTAGTAGACACGTGGTTTCACCGTGTTAG TTTTTA T RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:32436310..32436394 26863410 MeRIP-seq:(Medium) rs1398760663 Functional Loss DEL dbSNP153 29..33 33 - - - 65798 RMVar_ID_65798 Human_SNP_ID_227025984 m1A Human chr5 + 32436327 32436327 32436327 CCCACCACCACGCCCGGCTGATTTTTTTTTTTATTTTTAGTAGACACGTGGTTTCACCGTGTTAG CCCACCACCACGCCCGGCTGATTTTTTTTTTTGTTTTTAGTAGACACGTGGTTTCACCGTGTTAG A G RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:32436310..32436394 26863410 MeRIP-seq:(Medium) rs1330975067 Functional Loss SNV dbSNP153 33..33 33 - - - 65799 RMVar_ID_65799 Human_SNP_ID_227025985 m1A Human chr5 + 32436327 32436327 32436327 CCCACCACCACGCCCGGCTGATTTTTTTTTTTATTTTTAGTAGACACGTGGTTTCACCGTGTTAG CCCACCACCACGCCCGGCTGATTTTTTTTTTTTTTTTTAGTAGACACGTGGTTTCACCGTGTTAG A T RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:32436310..32436394 26863410 MeRIP-seq:(Medium) rs1330975067 Functional Loss SNV dbSNP153 33..33 33 - - - 65800 RMVar_ID_65800 Human_SNP_ID_227028347 m1A Human chr5 - 32444672 32444672 32444672 AGGCAGCGGGTGAGAGTTCAGAGTTCAGCAGCAGCAGCCCGAGCCCATGATTCCCATATGCCCTG AGGCAGCGGGTGAGAGTTCAGAGTTCAGCAGCGGCAGCCCGAGCCCATGATTCCCATATGCCCTG T C ZFR Ensembl:ENSG00000056097 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:32444485..32444731;chr5:32444601..32444750 26863196 MeRIP-seq:(Medium) rs751056160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73698,Human_RBP_ID_787381,Human_RBP_ID_1212570,Human_RBP_ID_1653585,Human_RBP_ID_1994560,Human_RBP_ID_4829060,Human_RBP_ID_5610838,Human_RBP_ID_7430230,Human_RBP_ID_8614045,Human_RBP_ID_9306406,Human_RBP_ID_18448735,Human_RBP_ID_24385467 Human_Splice_Rec_640715,Human_Splice_Rec_640785 Human_miRNA_ID_1200928,Human_miRNA_ID_1230346,Human_miRNA_ID_2276320,Human_miRNA_ID_2579568 65801 RMVar_ID_65801 Human_SNP_ID_227028358 m1A Human chr5 + 32444687 32444687 32444687 TCATGGGCTCGGGCTGCTGCTGCTGAACTCTGAACTCTCACCCGCTGCCTCCCTCCTCTGCCCCG TCATGGGCTCGGGCTGCTGCTGCTGAACTCTGCACTCTCACCCGCTGCCTCCCTCCTCTGCCCCG A C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:32444588..32444725 26863196 MeRIP-seq:(Medium) rs1321403670 Functional Loss SNV dbSNP153 33..33 33 - - - 65802 RMVar_ID_65802 Human_SNP_ID_227063174 m1A Human chr5 + 32585618 32585618 32585618 ACGACCAAGAGGGTGTTCGACTGCTAGAGCCGAGCGAAGCGTGAGTGCGCGGGACCCCCTACCCC ACGACCAAGAGGGTGTTCGACTGCTAGAGCCGCGCGAAGCGTGAGTGCGCGGGACCCCCTACCCC A C SUB1 Ensembl:ENSG00000113387 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:32585551..32585689 26863196 MeRIP-seq:(Medium) rs527949327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641205,Human_RBP_ID_789198,Human_RBP_ID_1321318,Human_RBP_ID_1391405,Human_RBP_ID_1653600,Human_RBP_ID_4845646,Human_RBP_ID_5477068,Human_RBP_ID_7430299,Human_RBP_ID_8889422,Human_RBP_ID_9335192,Human_RBP_ID_15429055,Human_RBP_ID_18056727,Human_RBP_ID_22459511,Human_RBP_ID_24103439 Human_Splice_Rec_640825,Human_Splice_Rec_640833,Human_Splice_Rec_640843,Human_Splice_Rec_640853 RMVar_hsa_circ_230711,RMVar_hsa_circ_333743,RMVar_hsa_circ_35709,RMVar_hsa_circ_230715 65803 RMVar_ID_65803 Human_SNP_ID_227063311 m1A Human chr5 + 32585926 32585924 32585926 TGAGGGCGGCCGGGGAGTGAGGAGTCGCGGGGAGAGAGTCGCGGCGTCCCCGGGACAATGCGGCG TGAGGGCGGCCGGGGAGTGAGGAGTCGCGGG__GAGAGTCGCGGCGTCCCCGGGACAATGCGGCG GGA G SUB1 Ensembl:ENSG00000113387 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:32585919..32586001 26863196 MeRIP-seq:(Medium) rs1561030786 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_250652,Human_RBP_ID_1069479,Human_RBP_ID_5397202,Human_RBP_ID_8730224,Human_RBP_ID_9436524,Human_RBP_ID_18465339,Human_RBP_ID_18501707,Human_RBP_ID_18955895,Human_RBP_ID_21214288,Human_RBP_ID_26791737,Human_RBP_ID_27842065 Human_Splice_Rec_640863,Human_Splice_Rec_640869 RMVar_hsa_circ_230711,RMVar_hsa_circ_333743,RMVar_hsa_circ_35709,RMVar_hsa_circ_230715 65804 RMVar_ID_65804 Human_SNP_ID_227064185 m1A Human chr5 - 32588503 32588503 32588503 ACAAGTTCCTTTGATTTAGGCATCCTGAAAGAAAAATACATTACAAAAATAATTAATAAGGTACT ACAAGTTCCTTTGATTTAGGCATCCTGAAAGACAAATACATTACAAAAATAATTAATAAGGTACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:32588501..32588550 26863196 MeRIP-seq:(Medium) rs1242923598 Functional Loss SNV dbSNP153 33..33 33 - - - 65805 RMVar_ID_65805 Human_SNP_ID_227064190 m1A Human chr5 + 32588525 32588525 32588525 TAATGTATTTTTCTTTCAGGATGCCTAAATCAAAGGAACTTGTTTCTTCAAGCTCTTCTGGCAGT TAATGTATTTTTCTTTCAGGATGCCTAAATCAGAGGAACTTGTTTCTTCAAGCTCTTCTGGCAGT A G SUB1 Ensembl:ENSG00000113387 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:32588501..32588550 26863196 MeRIP-seq:(Medium) rs765529460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641209,Human_RBP_ID_2925735,Human_RBP_ID_4845647,Human_RBP_ID_9335194,Human_RBP_ID_18056728,Human_RBP_ID_22459512,Human_RBP_ID_24103445,Human_RBP_ID_26525967 Human_Splice_Rec_640798,Human_Splice_Rec_640799,Human_Splice_Rec_640808,Human_Splice_Rec_640809,Human_Splice_Rec_640826,Human_Splice_Rec_640827,Human_Splice_Rec_640834,Human_Splice_Rec_640835,Human_Splice_Rec_640846,Human_Splice_Rec_640847,Human_Splice_Rec_640856,Human_Splice_Rec_640857,Human_Splice_Rec_640866,Human_Splice_Rec_640867,Human_Splice_Rec_640876,Human_Splice_Rec_640877,Human_Splice_Rec_640879 RMVar_hsa_circ_72716,RMVar_hsa_circ_230711,RMVar_hsa_circ_333743,RMVar_hsa_circ_35709,RMVar_hsa_circ_230715 65806 RMVar_ID_65806 Human_SNP_ID_227065126 m1A Human chr5 + 32591651 32591651 32591651 TGAGACTTCGAGAGCCCTGTCATCTTCTAAACAGAGCAGCAGCAGCAGAGATGATAACATGTTTC TGAGACTTCGAGAGCCCTGTCATCTTCTAAACGGAGCAGCAGCAGCAGAGATGATAACATGTTTC A G SUB1 Ensembl:ENSG00000113387 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:32591600..32591729 26863196 MeRIP-seq:(Medium) rs142204481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641211,Human_RBP_ID_788620,Human_RBP_ID_1041244,Human_RBP_ID_1653613,Human_RBP_ID_1994570,Human_RBP_ID_7430394,Human_RBP_ID_8614073,Human_RBP_ID_15429315,Human_RBP_ID_18047165,Human_RBP_ID_18841511,Human_RBP_ID_19124380,Human_RBP_ID_22460004,Human_RBP_ID_22512309,Human_RBP_ID_22828411,Human_RBP_ID_27739785 Human_Splice_Rec_640800,Human_Splice_Rec_640801,Human_Splice_Rec_640810,Human_Splice_Rec_640811,Human_Splice_Rec_640820,Human_Splice_Rec_640821,Human_Splice_Rec_640828,Human_Splice_Rec_640829,Human_Splice_Rec_640836,Human_Splice_Rec_640837,Human_Splice_Rec_640848,Human_Splice_Rec_640849,Human_Splice_Rec_640858,Human_Splice_Rec_640859,Human_Splice_Rec_640868,Human_Splice_Rec_640870,Human_Splice_Rec_640871,Human_Splice_Rec_640878,Human_Splice_Rec_640880,Human_Splice_Rec_640881,Human_Splice_Rec_640883 Human_miRNA_ID_1768789 RMVar_hsa_circ_72716,RMVar_hsa_circ_230711,RMVar_hsa_circ_333743,RMVar_hsa_circ_230715 65807 RMVar_ID_65807 Human_SNP_ID_227095283 m1A Human chr5 + 32710953 32710953 32710953 TGTGCGTGCGCGCGCGCATTTCTCTACTTTAAAGCACGTTTCCTTTTTTGAAGCCAGGAGCTGGA TGTGCGTGCGCGCGCGCATTTCTCTACTTTAAGGCACGTTTCCTTTTTTGAAGCCAGGAGCTGGA A G NPR3 Ensembl:ENSG00000113389 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:32710951..32711158 26863196 MeRIP-seq:(Medium) rs1050985717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15431304 65808 RMVar_ID_65808 Human_SNP_ID_227111823 m1A Human chr5 + 32776853 32776853 32776853 CTATAAAATAAGGTAGGATAGGGAGCTAGAAAATGCCAGGCAAGGAGGAGTAGGGCTGCTAGTTT CTATAAAATAAGGTAGGATAGGGAGCTAGAAAGTGCCAGGCAAGGAGGAGTAGGGCTGCTAGTTT A G NPR3 Ensembl:ENSG00000113389 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:32776851..32776947 26863196 MeRIP-seq:(Medium) rs1188231186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230718,RMVar_hsa_circ_230719,RMVar_hsa_circ_320791 65809 RMVar_ID_65809 Human_SNP_ID_227273848 m1A Human chr5 + 33445374 33445371 33445374 AAGCAAAAGGAAGGAGGCAAAAAGAAGAACAAAGAAGGATCTGGAGATGGAGGTCGAGCTGAGGT AAGCAAAAGGAAGGAGGCAAAAAGAAGAAC___GAAGGATCTGGAGATGGAGGTCGAGCTGAGGT CAAA C TARS1 Ensembl:ENSG00000113407 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:33445270..33445458;chr5:33445274..33445459 26863196 MeRIP-seq:(Medium) rs753206423 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_12636,Human_RBP_ID_77586,Human_RBP_ID_214038,Human_RBP_ID_250656,Human_RBP_ID_789200,Human_RBP_ID_1994611,Human_RBP_ID_4829184,Human_RBP_ID_5610841,Human_RBP_ID_7431403,Human_RBP_ID_8267562,Human_RBP_ID_8614374,Human_RBP_ID_8943829,Human_RBP_ID_9349557,Human_RBP_ID_9397737,Human_RBP_ID_15431880,Human_RBP_ID_18841605,Human_RBP_ID_23116214,Human_RBP_ID_24103651,Human_RBP_ID_24548095,Human_RBP_ID_26350720,Human_RBP_ID_27825276 Human_Splice_Rec_641042,Human_Splice_Rec_641043,Human_Splice_Rec_641080,Human_Splice_Rec_641081,Human_Splice_Rec_641086,Human_Splice_Rec_641087,Human_Splice_Rec_641122,Human_Splice_Rec_641123,Human_Splice_Rec_641126,Human_Splice_Rec_641127,Human_Splice_Rec_641160,Human_Splice_Rec_641161,Human_Splice_Rec_641198,Human_Splice_Rec_641199,Human_Splice_Rec_641232,Human_Splice_Rec_641233,Human_Splice_Rec_641268,Human_Splice_Rec_641269,Human_Splice_Rec_641276,Human_Splice_Rec_641277,Human_Splice_Rec_641284,Human_Splice_Rec_641285,Human_Splice_Rec_641288,Human_Splice_Rec_641289,Human_Splice_Rec_641292,Human_Splice_Rec_641293 RMVar_hsa_circ_51632 65810 RMVar_ID_65810 Human_SNP_ID_227273848 m1A Human chr5 + 33445373 33445371 33445374 GAAGCAAAAGGAAGGAGGCAAAAAGAAGAACAAAGAAGGATCTGGAGATGGAGGTCGAGCTGAGG GAAGCAAAAGGAAGGAGGCAAAAAGAAGAAC___GAAGGATCTGGAGATGGAGGTCGAGCTGAGG CAAA C TARS1 Ensembl:ENSG00000113407 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:33445260..33446097 26863196 MeRIP-seq:(Medium) rs753206423 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12636,Human_RBP_ID_77586,Human_RBP_ID_214038,Human_RBP_ID_250656,Human_RBP_ID_789200,Human_RBP_ID_1994611,Human_RBP_ID_4829184,Human_RBP_ID_5610841,Human_RBP_ID_7431403,Human_RBP_ID_8267562,Human_RBP_ID_8614374,Human_RBP_ID_8943829,Human_RBP_ID_9349557,Human_RBP_ID_9397737,Human_RBP_ID_15431880,Human_RBP_ID_18841605,Human_RBP_ID_23116214,Human_RBP_ID_24103651,Human_RBP_ID_24548095,Human_RBP_ID_26350720,Human_RBP_ID_27825276 Human_Splice_Rec_641042,Human_Splice_Rec_641043,Human_Splice_Rec_641080,Human_Splice_Rec_641081,Human_Splice_Rec_641086,Human_Splice_Rec_641087,Human_Splice_Rec_641122,Human_Splice_Rec_641123,Human_Splice_Rec_641126,Human_Splice_Rec_641127,Human_Splice_Rec_641160,Human_Splice_Rec_641161,Human_Splice_Rec_641198,Human_Splice_Rec_641199,Human_Splice_Rec_641232,Human_Splice_Rec_641233,Human_Splice_Rec_641268,Human_Splice_Rec_641269,Human_Splice_Rec_641276,Human_Splice_Rec_641277,Human_Splice_Rec_641284,Human_Splice_Rec_641285,Human_Splice_Rec_641288,Human_Splice_Rec_641289,Human_Splice_Rec_641292,Human_Splice_Rec_641293 RMVar_hsa_circ_51632 65811 RMVar_ID_65811 Human_SNP_ID_227273849 m1A Human chr5 + 33445373 33445371 33445373 GAAGCAAAAGGAAGGAGGCAAAAAGAAGAACAAAGAAGGATCTGGAGATGGAGGTCGAGCTGAGG GAAGCAAAAGGAAGGAGGCAAAAAGAAGAAC__AGAAGGATCTGGAGATGGAGGTCGAGCTGAGG CAA C TARS1 Ensembl:ENSG00000113407 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:33445260..33446097 26863196 MeRIP-seq:(Medium) rs1427284413 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12636,Human_RBP_ID_77586,Human_RBP_ID_214038,Human_RBP_ID_250656,Human_RBP_ID_789200,Human_RBP_ID_1994611,Human_RBP_ID_4829184,Human_RBP_ID_5610841,Human_RBP_ID_7431403,Human_RBP_ID_8267562,Human_RBP_ID_8614374,Human_RBP_ID_8943829,Human_RBP_ID_9349557,Human_RBP_ID_9397737,Human_RBP_ID_15431880,Human_RBP_ID_18841605,Human_RBP_ID_23116214,Human_RBP_ID_24103651,Human_RBP_ID_24548095,Human_RBP_ID_26350720,Human_RBP_ID_27825276 Human_Splice_Rec_641042,Human_Splice_Rec_641043,Human_Splice_Rec_641080,Human_Splice_Rec_641081,Human_Splice_Rec_641086,Human_Splice_Rec_641087,Human_Splice_Rec_641122,Human_Splice_Rec_641123,Human_Splice_Rec_641126,Human_Splice_Rec_641127,Human_Splice_Rec_641160,Human_Splice_Rec_641161,Human_Splice_Rec_641198,Human_Splice_Rec_641199,Human_Splice_Rec_641232,Human_Splice_Rec_641233,Human_Splice_Rec_641268,Human_Splice_Rec_641269,Human_Splice_Rec_641276,Human_Splice_Rec_641277,Human_Splice_Rec_641284,Human_Splice_Rec_641285,Human_Splice_Rec_641288,Human_Splice_Rec_641289,Human_Splice_Rec_641292,Human_Splice_Rec_641293 RMVar_hsa_circ_51632 65812 RMVar_ID_65812 Human_SNP_ID_227274584 m1A Human chr5 + 33448495 33448495 33448495 ATTATTTCTTTCCCATTTCTAAATAGGAAAGCAATATTTACTGATCATTTATTTCCTGATTTGTT ATTATTTCTTTCCCATTTCTAAATAGGAAAGCGATATTTACTGATCATTTATTTCCTGATTTGTT A G TARS1 Ensembl:ENSG00000113407 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:33448491..33448657 26863196 MeRIP-seq:(Medium) rs773796616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7431476 RMVar_hsa_circ_51632 65813 RMVar_ID_65813 Human_SNP_ID_227274615 m1A Human chr5 + 33448600 33448600 33448600 ACACGTCTTGAGATGTATAATATACTAAAAGCAGAACATGATTCCATTCTGGCAGAAAAGGCAGA ACACGTCTTGAGATGTATAATATACTAAAAGCGGAACATGATTCCATTCTGGCAGAAAAGGCAGA A G TARS1 Ensembl:ENSG00000113407 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:33448526..33448650;chr5:33448487..33448632 26863196 MeRIP-seq:(Medium) rs764780043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641359,Human_RBP_ID_1994613,Human_RBP_ID_2926131,Human_RBP_ID_3768561,Human_RBP_ID_5610843,Human_RBP_ID_9397740,Human_RBP_ID_23044617,Human_RBP_ID_24103670,Human_RBP_ID_27081492,Human_RBP_ID_27739900 Human_Splice_Rec_641044,Human_Splice_Rec_641082,Human_Splice_Rec_641088,Human_Splice_Rec_641162,Human_Splice_Rec_641200,Human_Splice_Rec_641236,Human_Splice_Rec_641270,Human_Splice_Rec_641280,Human_Splice_Rec_641294 RMVar_hsa_circ_51632,RMVar_hsa_circ_15076,RMVar_hsa_circ_336872,RMVar_hsa_circ_344957,RMVar_hsa_circ_52425,RMVar_hsa_circ_230721 65814 RMVar_ID_65814 Human_SNP_ID_227279725 m1A Human chr5 + 33467740 33467740 33467740 ATGAAAAAATTACCCAGATTGGCTCCATGGAAAAGGAGGAACAGCGTTTCCGTAAAATTGACTTT ATGAAAAAATTACCCAGATTGGCTCCATGGAAGAGGAGGAACAGCGTTTCCGTAAAATTGACTTT A G TARS1 Ensembl:ENSG00000113407 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs765717810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641373,Human_RBP_ID_789071,Human_RBP_ID_1653880,Human_RBP_ID_1994669,Human_RBP_ID_3768609,Human_RBP_ID_7431708,Human_RBP_ID_15432594,Human_RBP_ID_17708040,Human_RBP_ID_24103743,Human_RBP_ID_27336390 RMVar_hsa_circ_230731 65815 RMVar_ID_65815 Human_SNP_ID_227421654 m1A Human chr5 - 34063342 34063338 34063342 GAGAGGAGAGAGACAGAGACAGAGGAGAGAGAAAGAGAGACAGAGAGAGAAAAGGGAGAGAGAAG GAGAGGAGAGAGACAGAGACAGAGGAGAGAGA____GAGACAGAGAGAGAAAAGGGAGAGAGAAG CTCTT C C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:34063216..34063414 26863196 MeRIP-seq:(Medium) rs1242121502 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_56125,RMVar_hsa_circ_230754,RMVar_hsa_circ_289277 65816 RMVar_ID_65816 Human_SNP_ID_227421662 m1A Human chr5 - 34063362 34063362 34063362 CGAGGAGAGAGAAAGAGACAGAGAGGAGAGAGACAGAGACAGAGGAGAGAGAAAGAGAGACAGAG CGAGGAGAGAGAAAGAGACAGAGAGGAGAGAGCCAGAGACAGAGGAGAGAGAAAGAGAGACAGAG T G C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:34063210..34063428 26863196 MeRIP-seq:(Medium) rs1561068994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12270,Human_RBP_ID_25890861 RMVar_hsa_circ_56125,RMVar_hsa_circ_230754,RMVar_hsa_circ_289277 65817 RMVar_ID_65817 Human_SNP_ID_227449071 m1A Human chr5 + 34191417 34191417 34191417 GGGGCCAGCCTCATCCCACTGCCAGCTGGCCCACAGTTCCTCAAAGACAGTGAGTGAGGACGGAC GGGGCCAGCCTCATCCCACTGCCAGCTGGCCCTCAGTTCCTCAAAGACAGTGAGTGAGGACGGAC A T AC138409.1 Ensembl:ENSG00000215156 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:34191354..34191455 32194978 MeRIP-seq:(Medium) rs1390283350 Functional Loss SNV dbSNP153 33..33 33 - - - 65818 RMVar_ID_65818 Human_SNP_ID_227449275 m1A Human chr5 + 34192281 34192281 34192281 TGAGGACGGACCTCAGGCTGTCTCTTCGCGTCACACCCGCTGTGAAAAGGCAGATACAGCACCAG TGAGGACGGACCTCAGGCTGTCTCTTCGCGTCGCACCCGCTGTGAAAAGGCAGATACAGCACCAG A G AC138409.1 Ensembl:ENSG00000215156 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:34192103..34192404 32194978 MeRIP-seq:(Medium) rs1391442931 Functional Loss SNV dbSNP153 33..33 33 - - - 65819 RMVar_ID_65819 Human_SNP_ID_227560203 m1A Human chr5 - 34656429 34656429 34656429 GGCGGCGCTCCCCGGACCCAGCTGGCTGCTCCACCCCGCCCGCCGCTTCCCCAGGAAAACGCGGC GGCGGCGCTCCCCGGACCCAGCTGGCTGCTCCCCCCCGCCCGCCGCTTCCCCAGGAAAACGCGGC T G AC025754.1 Ensembl:ENSG00000250234 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:34656257..34657115 26863196 MeRIP-seq:(Medium) rs930700005 Functional Loss SNV dbSNP153 33..33 33 - - - 65820 RMVar_ID_65820 Human_SNP_ID_227583794 m1A Human chr5 - 34757421 34757421 34757421 AAGAAACAGAGGTCATGAACAACACTGGCCACAGCCGCACTGACCAGCAGGGCTGCAGTCCTCGC AAGAAACAGAGGTCATGAACAACACTGGCCACGGCCGCACTGACCAGCAGGGCTGCAGTCCTCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:34757417..34757498 26863196 MeRIP-seq:(Medium) rs751137165 Functional Loss SNV dbSNP153 33..33 33 - - - 65821 RMVar_ID_65821 Human_SNP_ID_227595756 m1A Human chr5 - 34807492 34807492 34807492 GGCTCTCTCATCTTAATCCTTTCTTTTCCCCCATCTCCTGCCCTTTCTGTCCCCCTTCACGAAAC GGCTCTCTCATCTTAATCCTTTCTTTTCCCCCTTCTCCTGCCCTTTCTGTCCCCCTTCACGAAAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:34807485..34807565 26863196 MeRIP-seq:(Medium) rs907809119 Functional Loss SNV dbSNP153 33..33 33 - - - 65822 RMVar_ID_65822 Human_SNP_ID_227621021 m1A Human chr5 + 34915748 34915748 34915748 AAGAGCGCGGGCGGCGAGGCAAGATGGCGGCAACCAAGAGGAAACGGCGTGGAGGCTTTGCAGTT AAGAGCGCGGGCGGCGAGGCAAGATGGCGGCAGCCAAGAGGAAACGGCGTGGAGGCTTTGCAGTT A G BRIX1 Ensembl:ENSG00000113460 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:34915726..34915865 26863196 MeRIP-seq:(Medium) rs1313491018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77885,Human_RBP_ID_4829582,Human_RBP_ID_9397751,Human_RBP_ID_18424939,Human_RBP_ID_22458820,Human_RBP_ID_26350739,Human_RBP_ID_27825297 65823 RMVar_ID_65823 Human_SNP_ID_227621026 m1A Human chr5 + 34915751 34915751 34915751 AGCGCGGGCGGCGAGGCAAGATGGCGGCAACCAAGAGGAAACGGCGTGGAGGCTTTGCAGTTCAG AGCGCGGGCGGCGAGGCAAGATGGCGGCAACCGAGAGGAAACGGCGTGGAGGCTTTGCAGTTCAG A G BRIX1 Ensembl:ENSG00000113460 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:34915701..34915875 26863196 MeRIP-seq:(Medium) rs41270681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77885,Human_RBP_ID_4829582,Human_RBP_ID_7432590,Human_RBP_ID_9397751,Human_RBP_ID_18424939,Human_RBP_ID_22458820,Human_RBP_ID_26350739,Human_RBP_ID_27825297 65824 RMVar_ID_65824 Human_SNP_ID_227621049 m1A Human chr5 - 34915774 34915774 34915774 TCGTTTCTTTTTGGCTTCTTCGCCTGAACTGCAAAGCCTCCACGCCGTTTCCTCTTGGTTGCCGC TCGTTTCTTTTTGGCTTCTTCGCCTGAACTGCTAAGCCTCCACGCCGTTTCCTCTTGGTTGCCGC T A RAD1 Ensembl:ENSG00000113456 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:34915351..34919900 26863196 MeRIP-seq:(Medium) rs1407998439 Functional Loss SNV dbSNP153 33..33 33 - - - 65825 RMVar_ID_65825 Human_SNP_ID_227624769 m1A Human chr5 + 34929734 34929734 34929734 CGGGCGGCGGACTCCCGCCGGAGAGGACTGCCAGCGCCGCCGCCGCCGCCGCTTCGGCCCGGGCC CGGGCGGCGGACTCCCGCCGGAGAGGACTGCCGGCGCCGCCGCCGCCGCCGCTTCGGCCCGGGCC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:34929651..34929875;chr5:34929243..34929955;chr5:34929264..34933840 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1011270040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4829627 65826 RMVar_ID_65826 Human_SNP_ID_227624852 m1A Human chr5 + 34929857 34929857 34929857 GTGTCACTATGAGGCGCTGGGGGTGCGGCGCGACGCCAGCGAGGAGGAGCTCAAGAAGGCCTATC GTGTCACTATGAGGCGCTGGGGGTGCGGCGCGGCGCCAGCGAGGAGGAGCTCAAGAAGGCCTATC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:34929601..34929875 26863196 MeRIP-seq:(Medium) rs1335920677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4829635,Human_RBP_ID_18425246,Human_RBP_ID_22099350,Human_RBP_ID_26826213 Human_Splice_Rec_642269,Human_Splice_Rec_642291,Human_Splice_Rec_642315 Human_miRNA_ID_1690696 65827 RMVar_ID_65827 Human_SNP_ID_227624854 m1A Human chr5 + 34929862 34929862 34929862 ACTATGAGGCGCTGGGGGTGCGGCGCGACGCCAGCGAGGAGGAGCTCAAGAAGGCCTATCGGAAG ACTATGAGGCGCTGGGGGTGCGGCGCGACGCCCGCGAGGAGGAGCTCAAGAAGGCCTATCGGAAG A C DNAJC21 Ensembl:ENSG00000168724 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:34929571..34929900;chr5:34929601..34929875 26863196 MeRIP-seq:(Medium) rs1441391830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4829635,Human_RBP_ID_18425246,Human_RBP_ID_22099350,Human_RBP_ID_26826213 Human_Splice_Rec_642269,Human_Splice_Rec_642291,Human_Splice_Rec_642315 Human_miRNA_ID_1690696 65828 RMVar_ID_65828 Human_SNP_ID_227626932 m1A Human chr5 + 34937621 34937621 34937621 AGCCGAAGAGATGAGGCGGCAGCAGAAGCTAAAGCAGGCCAAGTGCGTAGCGTGCGTGGGGCCCT AGCCGAAGAGATGAGGCGGCAGCAGAAGCTAAGGCAGGCCAAGTGCGTAGCGTGCGTGGGGCCCT A G DNAJC21 Ensembl:ENSG00000168724 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:34937394..34941200 26863196 MeRIP-seq:(Medium) rs1303623051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9397754,Human_RBP_ID_26350750,Human_RBP_ID_27825301 Human_Splice_Rec_642277,Human_Splice_Rec_642299,Human_Splice_Rec_642323,Human_Splice_Rec_642345,Human_Splice_Rec_642367,Human_Splice_Rec_642387,Human_Splice_Rec_642411,Human_Splice_Rec_642427 RMVar_hsa_circ_5869,RMVar_hsa_circ_368305 65829 RMVar_ID_65829 Human_SNP_ID_227627259 m1A Human chr5 - 34938937 34938937 34938937 TTCATCCGATCCATCTCCAAACTCCTTCTCGTACCGTGCCTCCATCTCCTGGAGCTCTTTCTCCA TTCATCCGATCCATCTCCAAACTCCTTCTCGTCCCGTGCCTCCATCTCCTGGAGCTCTTTCTCCA T G RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:34937419..34941215 26863196 MeRIP-seq:(Medium) rs1346041907 Functional Loss SNV dbSNP153 33..33 33 - - - 65830 RMVar_ID_65830 Human_SNP_ID_227916406 m1A Human chr5 - 36119748 36119748 36119748 AGGAGAGGAGATTTTAGAGATTTGAGGAGGGAAGAGAAGGTGCAAAATAGTTGCCTAGGAGAGTG AGGAGAGGAGATTTTAGAGATTTGAGGAGGGAGGAGAAGGTGCAAAATAGTTGCCTAGGAGAGTG T C LMBRD2 Ensembl:ENSG00000164187 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:36119615..36120039 26863196 MeRIP-seq:(Medium) rs1046148749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5543,RMVar_hsa_circ_363867,RMVar_hsa_circ_339302,RMVar_hsa_circ_18939,RMVar_hsa_circ_5932,RMVar_hsa_circ_6412,RMVar_hsa_circ_21635,RMVar_hsa_circ_230799,RMVar_hsa_circ_230800,RMVar_hsa_circ_230801,RMVar_hsa_circ_299227,RMVar_hsa_circ_72646,RMVar_hsa_circ_334253,RMVar_hsa_circ_268662,RMVar_hsa_circ_230802,RMVar_hsa_circ_52920,RMVar_hsa_circ_230804,RMVar_hsa_circ_314517,RMVar_hsa_circ_307222,RMVar_hsa_circ_368498,RMVar_hsa_circ_230805,RMVar_hsa_circ_230806 65831 RMVar_ID_65831 Human_SNP_ID_227916435 m1A Human chr5 - 36119872 36119872 36119872 GAACAATGAAGAGAATGGTGGAGGTAAGGCACAGATGTAACTAGCTGAGAAGGTGTAGTGTTAGA GAACAATGAAGAGAATGGTGGAGGTAAGGCACTGATGTAACTAGCTGAGAAGGTGTAGTGTTAGA T A LMBRD2 Ensembl:ENSG00000164187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:36119549..36119998 26863196 MeRIP-seq:(Medium) rs1421787497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5543,RMVar_hsa_circ_363867,RMVar_hsa_circ_339302,RMVar_hsa_circ_18939,RMVar_hsa_circ_5932,RMVar_hsa_circ_6412,RMVar_hsa_circ_21635,RMVar_hsa_circ_230799,RMVar_hsa_circ_230800,RMVar_hsa_circ_230801,RMVar_hsa_circ_299227,RMVar_hsa_circ_72646,RMVar_hsa_circ_334253,RMVar_hsa_circ_268662,RMVar_hsa_circ_230802,RMVar_hsa_circ_52920,RMVar_hsa_circ_230804,RMVar_hsa_circ_314517,RMVar_hsa_circ_307222,RMVar_hsa_circ_368498,RMVar_hsa_circ_230805,RMVar_hsa_circ_230806 65832 RMVar_ID_65832 Human_SNP_ID_227916712 m1A Human chr5 + 36120880 36120880 36120880 AAAACACTTCATTGTCCTAATTTTCCTATCTCACTGGCCCCTCCTTTTCTAGTCTTTTCTGCTAG AAAACACTTCATTGTCCTAATTTTCCTATCTCGCTGGCCCCTCCTTTTCTAGTCTTTTCTGCTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:36120859..36120924 26863196 MeRIP-seq:(Medium) rs1004644787 Functional Loss SNV dbSNP153 33..33 33 - - - 65833 RMVar_ID_65833 Human_SNP_ID_227923264 m1A Human chr5 - 36151661 36151661 36151661 TGAGGCGCTTTTGAGTCTGGGGTCCGGGGCCGAGAGCAGGCGGAAAGAGAGGGGACCCGGCAGAC TGAGGCGCTTTTGAGTCTGGGGTCCGGGGCCGGGAGCAGGCGGAAAGAGAGGGGACCCGGCAGAC T C LMBRD2 Ensembl:ENSG00000164187 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:36151618..36151889 26863196 MeRIP-seq:(Medium) rs979794727 Functional Loss SNV dbSNP153 33..33 33 - - - 65834 RMVar_ID_65834 Human_SNP_ID_227923419 m1A Human chr5 + 36152162 36152162 36152162 TAGGCTTAGCGGGTCTGGCTGCTGGGGGCCCGAGCAGCACGCTCGGAGCCGCCGCGCGCCAAAGC TAGGCTTAGCGGGTCTGGCTGCTGGGGGCCCGGGCAGCACGCTCGGAGCCGCCGCGCGCCAAAGC A G SKP2 Ensembl:ENSG00000145604 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:36152101..36152268 26863196 MeRIP-seq:(Medium) rs1448647562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250756,Human_RBP_ID_3967828,Human_RBP_ID_4845146,Human_RBP_ID_5276430,Human_RBP_ID_18047623,Human_RBP_ID_18424940,Human_RBP_ID_22459117 65835 RMVar_ID_65835 Human_SNP_ID_227923457 m1A Human chr5 + 36152227 36152227 36152227 GGGAATCTGGGAGGCGAGCAGCTCTGCAGTTAATGCACGTATTTTAAACTCCCGGGCCTGCGGAC GGGAATCTGGGAGGCGAGCAGCTCTGCAGTTAGTGCACGTATTTTAAACTCCCGGGCCTGCGGAC A G SKP2 Ensembl:ENSG00000145604 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:36152126..36152275 26863410 MeRIP-seq:(Medium) rs752975573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041356,Human_RBP_ID_1654099,Human_RBP_ID_3967828,Human_RBP_ID_4829812,Human_RBP_ID_5477070,Human_RBP_ID_7433231,Human_RBP_ID_18047625,Human_RBP_ID_22460014 Human_Splice_Rec_643447,Human_Splice_Rec_643465,Human_Splice_Rec_643479,Human_Splice_Rec_643497,Human_Splice_Rec_643515,Human_Splice_Rec_643523,Human_Splice_Rec_643533,Human_Splice_Rec_643547 65836 RMVar_ID_65836 Human_SNP_ID_227926140 m1A Human chr5 - 36163709 36163709 36163709 CTCTTACAAACACCAGAGACCTTTAGCAGCTCAGGGAGGCACAGACAGGAAAAGATTCCCAAGAG CTCTTACAAACACCAGAGACCTTTAGCAGCTCGGGGAGGCACAGACAGGAAAAGATTCCCAAGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:36163626..36168400 32194978 MeRIP-seq:(Medium) rs1207579470 Functional Loss SNV dbSNP153 33..33 33 - - - 65837 RMVar_ID_65837 Human_SNP_ID_227928539 m1A Human chr5 - 36174731 36174731 36174731 CTCCTCAGAGAGGCCCTGTCTTTAACCATTCCATCTAAAAGTAGTCCTCTTTCTGCCACATTCTA CTCCTCAGAGAGGCCCTGTCTTTAACCATTCCGTCTAAAAGTAGTCCTCTTTCTGCCACATTCTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:36174713..36174870 26863196 MeRIP-seq:(Medium) rs1249095946 Functional Loss SNV dbSNP153 33..33 33 - - - 65838 RMVar_ID_65838 Human_SNP_ID_227944013 m1A Human chr5 - 36241570 36241569 36241570 TCCGCCCCTCCCGGGTGGTGGTGGTGGCCAAAACCACCCGGTACGAGTTCGAGCAGCAGCGGTAC TCCGCCCCTCCCGGGTGGTGGTGGTGGCCAAA_CCACCCGGTACGAGTTCGAGCAGCAGCGGTAC GT G NADK2 Ensembl:ENSG00000152620 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:36241476..36241925 26863196 MeRIP-seq:(Medium) rs866913594 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4845147 Human_Splice_Rec_643563,Human_Splice_Rec_643711 65839 RMVar_ID_65839 Human_SNP_ID_227944070 m1A Human chr5 + 36241682 36241682 36241682 CCCTGCCCCAGGTGCCGCCGGCCGCCACCGTCACCGCCCAGCCGGGGCCGCGCGGCGGGGCCTCC CCCTGCCCCAGGTGCCGCCGGCCGCCACCGTCTCCGCCCAGCCGGGGCCGCGCGGCGGGGCCTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:36227501..36242030;chr5:36241476..36242030 26863196 MeRIP-seq:(Medium) rs1194619875 Functional Loss SNV dbSNP153 33..33 33 - - - 65840 RMVar_ID_65840 Human_SNP_ID_227944080 m1A Human chr5 - 36241712 36241712 36241712 CGGGCGGCGGCGCTGCGGGGACCGGGTGCGGGAGGCCCCGCCGCGCGGCCCCGGCTGGGCGGTGA CGGGCGGCGGCGCTGCGGGGACCGGGTGCGGGGGGCCCCGCCGCGCGGCCCCGGCTGGGCGGTGA T C NADK2 Ensembl:ENSG00000152620 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:36241501..36241925 26863196 MeRIP-seq:(Medium) rs1015672238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250814,Human_RBP_ID_4846333,Human_RBP_ID_5242389,Human_RBP_ID_8893498,Human_RBP_ID_9354567,Human_RBP_ID_24385864 65841 RMVar_ID_65841 Human_SNP_ID_228140694 m1A Human chr5 - 37055589 37055589 37055589 GCATCTGACTATTACCCACACTTTCCTTCATGAAATCTTCTTCCTAAGTTTTCTCTTCCTACCTC GCATCTGACTATTACCCACACTTTCCTTCATGGAATCTTCTTCCTAAGTTTTCTCTTCCTACCTC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:37055496..37055696 26863196 MeRIP-seq:(Medium) rs1421284436 Functional Loss SNV dbSNP153 33..33 33 - - - 65842 RMVar_ID_65842 Human_SNP_ID_228142731 m1A Human chr5 + 37063908 37063908 37063908 AATTACCTCACTGCTTGGAGGAGGCAGCCCTAAAAATAATACAGCAGCAGAGACAGAAGATGATG AATTACCTCACTGCTTGGAGGAGGCAGCCCTAGAAATAATACAGCAGCAGAGACAGAAGATGATG A G NIPBL Ensembl:ENSG00000164190 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:37063857..37064049 26863196 MeRIP-seq:(Medium) rs1262852273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12638,Human_RBP_ID_2928943,Human_RBP_ID_18047976,Human_RBP_ID_18195100,Human_RBP_ID_18842206,Human_RBP_ID_24105218,Human_RBP_ID_27740306 Human_Splice_Rec_644051 RMVar_hsa_circ_267508,RMVar_hsa_circ_111535,RMVar_hsa_circ_230888,RMVar_hsa_circ_80622,RMVar_hsa_circ_230889,RMVar_hsa_circ_74715 65843 RMVar_ID_65843 Human_SNP_ID_228160681 m1A Human chr5 - 37141143 37141143 37141143 CACTGAGGAGGCTACTAAAATCTGACCTGGGAAATAATGAGGGCCTGGCTAGTGTTGTGGGAAAG CACTGAGGAGGCTACTAAAATCTGACCTGGGAGATAATGAGGGCCTGGCTAGTGTTGTGGGAAAG T C CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:37141093..37141223 26863196 MeRIP-seq:(Medium) rs776929361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2422,RMVar_hsa_circ_332709,RMVar_hsa_circ_38793,RMVar_hsa_circ_72235,RMVar_hsa_circ_230892,RMVar_hsa_circ_316124,RMVar_hsa_circ_121317,RMVar_hsa_circ_72364,RMVar_hsa_circ_230897,RMVar_hsa_circ_58508,RMVar_hsa_circ_230900,RMVar_hsa_circ_299179,RMVar_hsa_circ_337070,RMVar_hsa_circ_313599,RMVar_hsa_circ_230901,RMVar_hsa_circ_230902,RMVar_hsa_circ_328119,RMVar_hsa_circ_21777,RMVar_hsa_circ_53571,RMVar_hsa_circ_4833,RMVar_hsa_circ_230907,RMVar_hsa_circ_305787,RMVar_hsa_circ_317015,RMVar_hsa_circ_336154,RMVar_hsa_circ_360383,RMVar_hsa_circ_319048,RMVar_hsa_circ_312617,RMVar_hsa_circ_19407,RMVar_hsa_circ_284650,RMVar_hsa_circ_230908,RMVar_hsa_circ_67676,RMVar_hsa_circ_230905,RMVar_hsa_circ_230906,RMVar_hsa_circ_316728,RMVar_hsa_circ_358823,RMVar_hsa_circ_72681,RMVar_hsa_circ_230909,RMVar_hsa_circ_10098,RMVar_hsa_circ_45799,RMVar_hsa_circ_230910,RMVar_hsa_circ_25842 65844 RMVar_ID_65844 Human_SNP_ID_228196603 m1A Human chr5 - 37291379 37291379 37291379 AAAATAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGGAGGCGAA AAAATAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGGAGGCGAA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs993068349 Functional Loss SNV dbSNP153 33..33 33 - - - 65845 RMVar_ID_65845 Human_SNP_ID_228219130 m1A Human chr5 - 37370979 37370979 37370979 CTTTTTCTGGACCCTGGTGTCTACGATTTCCGAGATGCCGTCTTCTTTGTTGGGCGCGGCGATGC CTTTTTCTGGACCCTGGTGTCTACGATTTCCGGGATGCCGTCTTCTTTGTTGGGCGCGGCGATGC T C NUP155 Ensembl:ENSG00000113569 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:37370929..37371050 26863196 MeRIP-seq:(Medium) rs201875454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_787655,Human_RBP_ID_1654494,Human_RBP_ID_1995329,Human_RBP_ID_4830980,Human_RBP_ID_5610949,Human_RBP_ID_8893506,Human_RBP_ID_9306966,Human_RBP_ID_9335204,Human_RBP_ID_15443307,Human_RBP_ID_18842459,Human_RBP_ID_21167435,Human_RBP_ID_22099365,Human_RBP_ID_22300945,Human_RBP_ID_22828469,Human_RBP_ID_23045135,Human_RBP_ID_23120186,Human_RBP_ID_23214145,Human_RBP_ID_25895055,Human_RBP_ID_27081874,Human_RBP_ID_27515792 RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 65846 RMVar_ID_65846 Human_SNP_ID_228219153 m1A Human chr5 + 37371025 37371025 37371025 CACCAGGGTCCAGAAAAAGTCAAAAACCAAGGAGAAACAAGAAAAGATCCAAGAAGTTAGCTTAG CACCAGGGTCCAGAAAAAGTCAAAAACCAAGGCGAAACAAGAAAAGATCCAAGAAGTTAGCTTAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr5:37371001..37371025;chr5:37370926..37371075 26863196,26863410 MeRIP-seq:(Medium) rs375874689 Functional Loss SNV dbSNP153 33..33 33 - - - 65847 RMVar_ID_65847 Human_SNP_ID_228219154 m1A Human chr5 + 37371025 37371025 37371025 CACCAGGGTCCAGAAAAAGTCAAAAACCAAGGAGAAACAAGAAAAGATCCAAGAAGTTAGCTTAG CACCAGGGTCCAGAAAAAGTCAAAAACCAAGGTGAAACAAGAAAAGATCCAAGAAGTTAGCTTAG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr5:37371001..37371025;chr5:37370926..37371075 26863196,26863410 MeRIP-seq:(Medium) rs375874689 Functional Loss SNV dbSNP153 33..33 33 - - - 65848 RMVar_ID_65848 Human_SNP_ID_228219185 m1A Human chr5 - 37371068 37371068 37371068 GCGCCAAGGCGCTCGTTTGGCGCGCGCGCCCTAGGCGGCGGATCTAAGCTAACTTCTTGGATCTT GCGCCAAGGCGCTCGTTTGGCGCGCGCGCCCTGGGCGGCGGATCTAAGCTAACTTCTTGGATCTT T C NUP155 Ensembl:ENSG00000113569 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:37371026..37371100 26863196 MeRIP-seq:(Medium) rs1008879084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4830982,Human_RBP_ID_8893980 Human_miRNA_ID_2895246 RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 65849 RMVar_ID_65849 Human_SNP_ID_228221425 m1A Human chr5 - 37379377 37379377 37379377 CGCCTCATGAAACCCACCTTCGCTGGGCCCAGAGCGCTCCATGGCTGGCCGCACACCCCAGAACC CGCCTCATGAAACCCACCTTCGCTGGGCCCAGGGCGCTCCATGGCTGGCCGCACACCCCAGAACC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:37379326..37379541 26863196 MeRIP-seq:(Medium) rs760410149 Functional Loss SNV dbSNP153 33..33 33 - - - 65850 RMVar_ID_65850 Human_SNP_ID_228221434 m1A Human chr5 + 37379391 37379391 37379391 CGGCCAGCCATGGAGCGCTCTGGGCCCAGCGAAGGTGGGTTTCATGAGGCGAGTCCGGGCGGGGT CGGCCAGCCATGGAGCGCTCTGGGCCCAGCGAGGGTGGGTTTCATGAGGCGAGTCCGGGCGGGGT A G WDR70 Ensembl:ENSG00000082068 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:37379348..37379540;chr5:37379362..37379470 26863196 MeRIP-seq:(Medium) rs1188797560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_645007,Human_Splice_Rec_645029,Human_Splice_Rec_645057,Human_Splice_Rec_645061 RMVar_hsa_circ_95615,RMVar_hsa_circ_231080,RMVar_hsa_circ_91922,RMVar_hsa_circ_231081 65851 RMVar_ID_65851 Human_SNP_ID_228268495 m1A Human chr5 + 37570015 37570014 37570015 AGTTCAGAGTATGATTAGAAACCAGGTTATGCAAGATGCTATAAGACATACTATTGTGGAGGGTA AGTTCAGAGTATGATTAGAAACCAGGTTATGC_AGATGCTATAAGACATACTATTGTGGAGGGTA CA C WDR70 Ensembl:ENSG00000082068 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:37570002..37570173 26863196 MeRIP-seq:(Medium) rs1441815761 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_95615,RMVar_hsa_circ_231080,RMVar_hsa_circ_91922,RMVar_hsa_circ_231081,RMVar_hsa_circ_90814,RMVar_hsa_circ_34780,RMVar_hsa_circ_341963,RMVar_hsa_circ_286733,RMVar_hsa_circ_112725,RMVar_hsa_circ_231086,RMVar_hsa_circ_231088,RMVar_hsa_circ_87167,RMVar_hsa_circ_231087,RMVar_hsa_circ_231085,RMVar_hsa_circ_50048,RMVar_hsa_circ_102548,RMVar_hsa_circ_231090,RMVar_hsa_circ_11748 65852 RMVar_ID_65852 Human_SNP_ID_228484514 m1A Human chr5 - 38466940 38466940 38466940 AGCCTGGCCAGCCTTCAACATGCTCTCCCCACAGCGGCTACCCAAAAGCCAGGCACAGATCCCAT AGCCTGGCCAGCCTTCAACATGCTCTCCCCACGGCGGCTACCCAAAAGCCAGGCACAGATCCCAT T C AC010457.1 Ensembl:ENSG00000251257 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:38466914..38466998 26863196 MeRIP-seq:(Medium) rs1321173328 Functional Loss SNV dbSNP153 33..33 33 - - - 65853 RMVar_ID_65853 Human_SNP_ID_228507229 m1A Human chr5 - 38556377 38556377 38556377 GGGCAGCCCCGGGGCGGCGGCCGAGGCTACAGAGCCGGCGGCAGGGGATGGCAAGATAGCGGCGC GGGCAGCCCCGGGGCGGCGGCCGAGGCTACAGGGCCGGCGGCAGGGGATGGCAAGATAGCGGCGC T C LIFR Ensembl:ENSG00000113594 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:38556326..38556604 26863196 MeRIP-seq:(Medium) rs1464230170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77995,Human_RBP_ID_4845150,Human_RBP_ID_18425101 Human_Splice_Rec_645467,Human_Splice_Rec_645585 65854 RMVar_ID_65854 Human_SNP_ID_228507483 m1A Human chr5 - 38556859 38556859 38556859 TTCTGAGAGCGGCCTCACCACCGGAGGCTCGGAGGAAGCACCACCCTCGGCGTCCGGGGCCCGTC TTCTGAGAGCGGCCTCACCACCGGAGGCTCGGCGGAAGCACCACCCTCGGCGTCCGGGGCCCGTC T G LIFR Ensembl:ENSG00000113594 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:38556808..38556897 26863196 MeRIP-seq:(Medium) rs1471750624 Functional Loss SNV dbSNP153 33..33 33 - - - 65855 RMVar_ID_65855 Human_SNP_ID_228575619 m1A Human chr5 - 38832105 38832069 38832105 GAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAAGGAGAGAGG GAGAGACAGAGAGAGAGACAGAGAGGAGAGAG_________________________________ CTCTCCTCTCTCCTTCTCTCTCTCCTCTCTCTCTCCT C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:38832032..38832231;chr5:38831974..38832289 26863196 MeRIP-seq:(Medium) rs1561314261 Functional Loss DEL dbSNP153 33..65 33 - - - 65856 RMVar_ID_65856 Human_SNP_ID_228575700 m1A Human chr5 - 38832105 38832105 38832105 GAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAAGGAGAGAGG GAGAGACAGAGAGAGAGACAGAGAGGAGAGAGGGGAGAGAGAGAGGAGAGAGAGAAGGAGAGAGG T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:38832032..38832231;chr5:38831974..38832289 26863196 MeRIP-seq:(Medium) rs75161136 Functional Loss SNV dbSNP153 33..33 33 - - - 65857 RMVar_ID_65857 Human_SNP_ID_228575716 m1A Human chr5 - 38832132 38832112 38832132 AGAGAGACAGAGAGACGGAGAGAGACAGAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGA AGAGAGACAGAGAGACGGAGAGAGACAGAGAG____________________GAGAGAGAGGAGA CCTCTCTGTCTCTCTCTCTGT C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:38831968..38832248 26863196 MeRIP-seq:(Medium) rs1561314426 Functional Loss DEL dbSNP153 33..52 33 - - - Human_RBP_ID_838773 65858 RMVar_ID_65858 Human_SNP_ID_228575722 m1A Human chr5 - 38832114 38832114 38832114 AGAGAGACAGAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAA AGAGAGACAGAGAGACAGAGAGAGAGACAGAGGGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAA T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr5:38831988..38832261;chr5:38832070..38832199 26863196 MeRIP-seq:(Medium) rs1223255978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25895761 65859 RMVar_ID_65859 Human_SNP_ID_228575761 m1A Human chr5 - 38832132 38832131 38832133 AGAGAGACAGAGAGACGGAGAGAGACAGAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGA AGAGAGACAGAGAGACGGAGAGAGACAGAGA__CAGAGAGAGAGACAGAGAGGAGAGAGAGGAGA GTC G OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:38831968..38832248 26863196 MeRIP-seq:(Medium) rs1337589642 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_838773 65860 RMVar_ID_65860 Human_SNP_ID_228578913 m1A Human chr5 - 38846128 38846128 38846128 GCAGAGCGGGGACGGGCGGGTCGGGGGTACTCACGCCGCGGGCGAAGGGCTCCACGAGCCGGGCC GCAGAGCGGGGACGGGCGGGTCGGGGGTACTCCCGCCGCGGGCGAAGGGCTCCACGAGCCGGGCC T G LINC01265 RNACentral:URS00008B41D4 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:38845857..38846316 26863196 MeRIP-seq:(Medium) rs1270434984 Functional Loss SNV dbSNP153 33..33 33 - - - 65861 RMVar_ID_65861 Human_SNP_ID_228629804 m1A Human chr5 - 39055186 39055186 39055186 GAGACAAGTAATAACTTGGAGAGGGTGGTACAACTGCAAAGGGAAGTCATTAGAGGGTTTCAGGC GAGACAAGTAATAACTTGGAGAGGGTGGTACAGCTGCAAAGGGAAGTCATTAGAGGGTTTCAGGC T C RICTOR Ensembl:ENSG00000164327 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:39055137..39055301 26863196 MeRIP-seq:(Medium) rs894593842 Functional Loss SNV dbSNP153 33..33 33 - - - 65862 RMVar_ID_65862 Human_SNP_ID_228712516 m1A Human chr5 + 39376974 39376974 39376974 GAGAGAGGAGTGCATGGATGGGGGCTGAGTGGACACAGCAGGAGCTGGAAAAATATTGCTCTGAA GAGAGAGGAGTGCATGGATGGGGGCTGAGTGGGCACAGCAGGAGCTGGAAAAATATTGCTCTGAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:39376951..39376975 26863196 MeRIP-seq:(Medium) rs1561364602 Functional Loss SNV dbSNP153 33..33 33 - - - 65863 RMVar_ID_65863 Human_SNP_ID_228713667 m1A Human chr5 + 39381522 39381522 39381522 TTGTTTTGAAGAGATCCAGAGGGTTGGGCTGCAGGGCTGTAGGTTGTCCTGTGGGTGACGCCTGG TTGTTTTGAAGAGATCCAGAGGGTTGGGCTGCGGGGCTGTAGGTTGTCCTGTGGGTGACGCCTGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:39381501..39381525 26863196 MeRIP-seq:(Medium) rs905892647 Functional Loss SNV dbSNP153 33..33 33 - - - 65864 RMVar_ID_65864 Human_SNP_ID_228713954 m1A Human chr5 + 39382667 39382667 39382667 CTCTTCCTGGTTTGGTACTTTGTGGAGGTGGGATAATGGCTATGGAGTCATGTGGTGAGGACTGG CTCTTCCTGGTTTGGTACTTTGTGGAGGTGGGTTAATGGCTATGGAGTCATGTGGTGAGGACTGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:39382575..39382887 26863196 MeRIP-seq:(Medium) rs1241739293 Functional Loss SNV dbSNP153 33..33 33 - - - 65865 RMVar_ID_65865 Human_SNP_ID_228723842 m1A Human chr5 + 39424920 39424920 39424920 TCGCTTAAATAGCCGCCGGCCGGGAGCTTCGGAGCCGCGCGGCCACTCCCGGCGAGAGATATGGT TCGCTTAAATAGCCGCCGGCCGGGAGCTTCGGCGCCGCGCGGCCACTCCCGGCGAGAGATATGGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:39424771..39425107;chr5:39424755..39424950;chr5:39424801..39424950 26863196 MeRIP-seq:(Medium) rs538557880 Functional Loss SNV dbSNP153 33..33 33 - - - 65866 RMVar_ID_65866 Human_SNP_ID_228723843 m1A Human chr5 + 39424920 39424920 39424920 TCGCTTAAATAGCCGCCGGCCGGGAGCTTCGGAGCCGCGCGGCCACTCCCGGCGAGAGATATGGT TCGCTTAAATAGCCGCCGGCCGGGAGCTTCGGGGCCGCGCGGCCACTCCCGGCGAGAGATATGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:39424771..39425107;chr5:39424755..39424950;chr5:39424801..39424950 26863196 MeRIP-seq:(Medium) rs538557880 Functional Loss SNV dbSNP153 33..33 33 - - - 65867 RMVar_ID_65867 Human_SNP_ID_228733795 m1A Human chr5 - 39462190 39462190 39462190 GGATGGAGATGGTAATAATCAGGGTTGGGTGGAGAATATCTGAGGAAACTGCACTTGATTTGGGC GGATGGAGATGGTAATAATCAGGGTTGGGTGGTGAATATCTGAGGAAACTGCACTTGATTTGGGC T A DAB2 Ensembl:ENSG00000153071 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:39462140..39462211 26863196 MeRIP-seq:(Medium) rs1379983657 Functional Loss SNV dbSNP153 33..33 33 - - - 65868 RMVar_ID_65868 Human_SNP_ID_229050437 m1A Human chr5 + 40679975 40679975 40679975 TCCAAGCCCGGCAGCCCGAGAGGAAGATGAACAGCCCCAGGCCAGAGCCTCTGGCAGAGTGGACC TCCAAGCCCGGCAGCCCGAGAGGAAGATGAACGGCCCCAGGCCAGAGCCTCTGGCAGAGTGGACC A G PTGER4 Ensembl:ENSG00000171522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:40679929..40680146 26863196 MeRIP-seq:(Medium) rs1286093656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127824,RMVar_hsa_circ_231173 65869 RMVar_ID_65869 Human_SNP_ID_229054428 m1A Human chr5 + 40697093 40697092 40697094 AAAAGAAAGAAAGGAAGGAAGGAAGGAAAGAAAGAGAAAAGAAAGAAAGGAAAGAAAAAAGAAAG AAAAGAAAGAAAGGAAGGAAGGAAGGAAAGAA__AGAAAAGAAAGAAAGGAAAGAAAAAAGAAAG AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:40697042..40697172 26863196 MeRIP-seq:(Medium) rs200191058 Functional Loss DEL dbSNP153 33..34 33 - - - 65870 RMVar_ID_65870 Human_SNP_ID_229059044 m1A Human chr5 + 40715578 40715578 40715578 AACACAAATCAGAATTAAGAGAAACTTCAGAAAATGTTCAGAATGTACACATTTGTGTGCATTTT AACACAAATCAGAATTAAGAGAAACTTCAGAAGATGTTCAGAATGTACACATTTGTGTGCATTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:40715442..40715593 32194978 MeRIP-seq:(Medium) rs903733159 Functional Loss SNV dbSNP153 33..33 33 - - - 65871 RMVar_ID_65871 Human_SNP_ID_229066552 m1A Human chr5 + 40746954 40746954 40746954 CTACATCCTTCTCATCAGCAGCTTCAGCTTCAAACTGCTGGGAAGTGACCTTTGAGACCTTCTCA CTACATCCTTCTCATCAGCAGCTTCAGCTTCACACTGCTGGGAAGTGACCTTTGAGACCTTCTCA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:40746822..40755875 32194978 MeRIP-seq:(Medium) rs752137248 Functional Loss SNV dbSNP153 33..33 33 - - - 65872 RMVar_ID_65872 Human_SNP_ID_229066553 m1A Human chr5 + 40746954 40746954 40746954 CTACATCCTTCTCATCAGCAGCTTCAGCTTCAAACTGCTGGGAAGTGACCTTTGAGACCTTCTCA CTACATCCTTCTCATCAGCAGCTTCAGCTTCAGACTGCTGGGAAGTGACCTTTGAGACCTTCTCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:40746822..40755875 32194978 MeRIP-seq:(Medium) rs752137248 Functional Loss SNV dbSNP153 33..33 33 - - - 65873 RMVar_ID_65873 Human_SNP_ID_229066559 m1A Human chr5 - 40746967 40746967 40746967 AGAGGAAAATTGGTGAGAAGGTCTCAAAGGTCACTTCCCAGCAGTTTGAAGCTGAAGCTGCTGAT AGAGGAAAATTGGTGAGAAGGTCTCAAAGGTCTCTTCCCAGCAGTTTGAAGCTGAAGCTGCTGAT T A TTC33 Ensembl:ENSG00000113638 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:40746916..40747058 26863196 MeRIP-seq:(Medium) rs1406015187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4855188 Human_Splice_Rec_646546,Human_Splice_Rec_646552,Human_Splice_Rec_646556,Human_Splice_Rec_646560,Human_Splice_Rec_646568,Human_Splice_Rec_646572,Human_Splice_Rec_646578 RMVar_hsa_circ_305529,RMVar_hsa_circ_231177,RMVar_hsa_circ_378010,RMVar_hsa_circ_48627,RMVar_hsa_circ_231181 65874 RMVar_ID_65874 Human_SNP_ID_229068727 m1A Human chr5 + 40755742 40755740 40755742 TCCTCAGCTTCCACCGCCGACCGGGCAGCCCCAGTTACCCGATAACGGCTCCCAAGGCCCCGTGT TCCTCAGCTTCCACCGCCGACCGGGCAGCCC__GTTACCCGATAACGGCTCCCAAGGCCCCGTGT CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:40755620..40755876 26863196 MeRIP-seq:(Medium) rs1350805279 Functional Loss DEL dbSNP153 32..33 33 - - - 65875 RMVar_ID_65875 Human_SNP_ID_229073822 m1A Human chr5 + 40777571 40777571 40777571 TGAGTATCTTCACAGCTACTTTATGCCCAGTCAATTCATGTTTGCCAACTGTAAAAGAAGTAATT TGAGTATCTTCACAGCTACTTTATGCCCAGTCCATTCATGTTTGCCAACTGTAAAAGAAGTAATT A C NONHSAG040254.2 RNACentral:URS00009B673D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:40777451..40777600 26863196 MeRIP-seq:(Medium) rs1198171523 Functional Loss SNV dbSNP153 33..33 33 - - - 65876 RMVar_ID_65876 Human_SNP_ID_229078864 m1A Human chr5 - 40798056 40798056 40798056 GGTCGGCACCTTCGGCAAAGTGAAGGGTGAGAACCCCGCGGGACTAGGCTTGGCCCCAGCTGAGG GGTCGGCACCTTCGGCAAAGTGAAGGGTGAGACCCCCGCGGGACTAGGCTTGGCCCCAGCTGAGG T G PRKAA1 Ensembl:ENSG00000132356 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:40798051..40798125 32194978 MeRIP-seq:(Medium) rs779754575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124409 65877 RMVar_ID_65877 Human_SNP_ID_229087004 m1A Human chr5 + 40827781 40827781 40827781 TGGAGTCTCGCTCTGCCGCCCGCCGTTCTCTCAGCTCACTGCAACCTCTGCCCCCCAGGCTCAAG TGGAGTCTCGCTCTGCCGCCCGCCGTTCTCTCCGCTCACTGCAACCTCTGCCCCCCAGGCTCAAG A C RF00017-4596 RNACentral:URS00009759B0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:40827702..40827892 26863196 MeRIP-seq:(Medium) rs940884041 Functional Loss SNV dbSNP153 33..33 33 - - - 65878 RMVar_ID_65878 Human_SNP_ID_229087477 m1A Human chr5 - 40829398 40829398 40829398 GGTGTAGGGTTGGTAAGAAAAGAATTCAGGGAAGAGCAGCGATCAGATTATGAAGAATTTGTCTT GGTGTAGGGTTGGTAAGAAAAGAATTCAGGGAGGAGCAGCGATCAGATTATGAAGAATTTGTCTT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:40829349..40829597 26863196 MeRIP-seq:(Medium) rs1406619976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12282,Human_RBP_ID_78251,Human_RBP_ID_7440053,Human_RBP_ID_10206044,Human_RBP_ID_15450983,Human_RBP_ID_18842880,Human_RBP_ID_23051888,Human_RBP_ID_24106403,Human_RBP_ID_25941726 Human_miRNA_ID_892066 65879 RMVar_ID_65879 Human_SNP_ID_229089384 m1A Human chr5 + 40835002 40835002 40835002 CAATGCGGCTCTAGCACCACAATTACGGCGGGATAGGTCCCCCAGGCACCAGTTAGCAGTCATTC CAATGCGGCTCTAGCACCACAATTACGGCGGGGTAGGTCCCCCAGGCACCAGTTAGCAGTCATTC A G RF00017-4596 RNACentral:URS00009759B0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:40834996..40835250 26863196 MeRIP-seq:(Medium) rs200838100 Functional Loss SNV dbSNP153 33..33 33 - - - 65880 RMVar_ID_65880 Human_SNP_ID_229089439 m1A Human chr5 + 40835124 40835123 40835125 GGAATCTTGCCAGCCCCCCAAGCACAGCAAACAGAGAGGCACAAAGGACGAGGATGGAACGCGAT GGAATCTTGCCAGCCCCCCAAGCACAGCAAAC__AGAGGCACAAAGGACGAGGATGGAACGCGAT CAG C RF00017-4596 RNACentral:URS00009759B0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:40835122..40835250 26863196 MeRIP-seq:(Medium) rs1561209630 Functional Loss DEL dbSNP153 33..34 33 - - - 65881 RMVar_ID_65881 Human_SNP_ID_229089479 m1A Human chr5 - 40835179 40835179 40835179 TTTCTGGTCTCGGCCGCAGAAGCGAGATGGTGAGTTGTGACTGTGGTGTTTGTGAATCGCGTTCC TTTCTGGTCTCGGCCGCAGAAGCGAGATGGTGGGTTGTGACTGTGGTGTTTGTGAATCGCGTTCC T C RPL37 Ensembl:ENSG00000145592 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr5:40835176..40835250;chr5:40835176..40835225 26863196,32194978 MeRIP-seq:(Medium) rs772138730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250151,Human_RBP_ID_839179,Human_RBP_ID_943345,Human_RBP_ID_1321669,Human_RBP_ID_4846354,Human_RBP_ID_9335210,Human_RBP_ID_17662385,Human_RBP_ID_18424946,Human_RBP_ID_19124413,Human_RBP_ID_24106469,Human_RBP_ID_26792060 RMVar_hsa_circ_86471,RMVar_hsa_circ_231194 65882 RMVar_ID_65882 Human_SNP_ID_229338542 m1A Human chr5 - 41805623 41805623 41805623 TGGGGAAGCCAAATCTGCTAAACCTGGAGATGACGTAAGGGAACGAATCATCAAGAGGGCCGCTC TGGGGAAGCCAAATCTGCTAAACCTGGAGATGGCGTAAGGGAACGAATCATCAAGAGGGCCGCTC T C OXCT1 Ensembl:ENSG00000083720 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:41805566..41807416 32194978 MeRIP-seq:(Medium) rs534151467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967193 Human_Splice_Rec_647196,Human_Splice_Rec_647197,Human_Splice_Rec_647238,Human_Splice_Rec_647239 RMVar_hsa_circ_73658,RMVar_hsa_circ_340632,RMVar_hsa_circ_231201,RMVar_hsa_circ_272265,RMVar_hsa_circ_275995,RMVar_hsa_circ_77946,RMVar_hsa_circ_3789,RMVar_hsa_circ_11519,RMVar_hsa_circ_231203,RMVar_hsa_circ_231202,RMVar_hsa_circ_281189,RMVar_hsa_circ_45857,RMVar_hsa_circ_34953,RMVar_hsa_circ_231207,RMVar_hsa_circ_284570,RMVar_hsa_circ_107058,RMVar_hsa_circ_231209,RMVar_hsa_circ_231210,RMVar_hsa_circ_110894,RMVar_hsa_circ_231212 65883 RMVar_ID_65883 Human_SNP_ID_229347108 m1A Human chr5 - 41844761 41844761 41844761 ACAGGATTTACTGGTAGATAGGTAAGGGGTGTAAGAGGAGTCAAGCATACTGTGTAAGATGAATG ACAGGATTTACTGGTAGATAGGTAAGGGGTGTGAGAGGAGTCAAGCATACTGTGTAAGATGAATG T C OXCT1 Ensembl:ENSG00000083720 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:41844757..41844849 26863196 MeRIP-seq:(Medium) rs980535044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73658,RMVar_hsa_circ_77946,RMVar_hsa_circ_11519,RMVar_hsa_circ_231202,RMVar_hsa_circ_45857,RMVar_hsa_circ_107058,RMVar_hsa_circ_231210,RMVar_hsa_circ_110894,RMVar_hsa_circ_231212,RMVar_hsa_circ_49186,RMVar_hsa_circ_23022,RMVar_hsa_circ_317316,RMVar_hsa_circ_45255,RMVar_hsa_circ_274902,RMVar_hsa_circ_373509,RMVar_hsa_circ_231213,RMVar_hsa_circ_104581,RMVar_hsa_circ_231214,RMVar_hsa_circ_231215 65884 RMVar_ID_65884 Human_SNP_ID_229347174 m1A Human chr5 + 41845039 41845039 41845039 ATTACATCACTCTCACCCTTATTCAAAACTCCATAGGCTTCCCACTGCGTTCCGTAAAATTCAAA ATTACATCACTCTCACCCTTATTCAAAACTCCGTAGGCTTCCCACTGCGTTCCGTAAAATTCAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:41845037..41845241 26863196 MeRIP-seq:(Medium) rs759804152 Functional Loss SNV dbSNP153 33..33 33 - - - 65885 RMVar_ID_65885 Human_SNP_ID_229353101 m1A Human chr5 + 41870375 41870375 41870375 GTTTGAGAGCCGCCATCTTCGGGCGGTGAGGCAGGAGGAGGCTGCGGGTTGGAGCGCGCGTTTGA GTTTGAGAGCCGCCATCTTCGGGCGGTGAGGCGGGAGGAGGCTGCGGGTTGGAGCGCGCGTTTGA A G AC034222.2,OXCT1-AS1 Ensembl:ENSG00000286164,Ensembl:ENSG00000248668 lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr5:41870326..41870486;chr5:41870326..41870453;chr5:41870176..41870423 26863196,32194978 MeRIP-seq:(Medium) rs1469204898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_647282,Human_Splice_Rec_647284,Human_Splice_Rec_647286 65886 RMVar_ID_65886 Human_SNP_ID_229353115 m1A Human chr5 - 41870391 41870391 41870391 AGTCGCGCACCGACGCTCAAACGCGCGCTCCAACCCGCAGCCTCCTCCTGCCTCACCGCCCGAAG AGTCGCGCACCGACGCTCAAACGCGCGCTCCAGCCCGCAGCCTCCTCCTGCCTCACCGCCCGAAG T C OXCT1 Ensembl:ENSG00000083720 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:41862688..41870475 26863196 MeRIP-seq:(Medium) rs776532355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845680 Human_miRNA_ID_847636,Human_miRNA_ID_1304122,Human_miRNA_ID_1386324,Human_miRNA_ID_2713190,Human_miRNA_ID_3049169 RMVar_hsa_circ_104581,RMVar_hsa_circ_231215 65887 RMVar_ID_65887 Human_SNP_ID_229364342 m1A Human chr5 - 41918351 41918351 41918351 TAAGAAGGAACTGAAGAATGTGGAATGAGCATAAAGGAGAGAAAAGTCAATAAAATAAGGAAGTG TAAGAAGGAACTGAAGAATGTGGAATGAGCATGAAGGAGAGAAAAGTCAATAAAATAAGGAAGTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:41918326..41918350 26863196 MeRIP-seq:(Medium) rs1473804529 Functional Loss SNV dbSNP153 33..33 33 - - - 65888 RMVar_ID_65888 Human_SNP_ID_229365988 m1A Human chr5 - 41925343 41925343 41925343 GCGGCCCCAGTCGCTGAAGGGCGGCGGCGGCGAGTTTGTTCCGCTGCGCGGCTCGCTTCCCGCCA GCGGCCCCAGTCGCTGAAGGGCGGCGGCGGCGGGTTTGTTCCGCTGCGCGGCTCGCTTCCCGCCA T C HSALNG0041434 RNACentral:URS0000EB3A65 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:41925302..41927015 26863196 MeRIP-seq:(Medium) rs961693227 Functional Loss SNV dbSNP153 33..33 33 - - - 65889 RMVar_ID_65889 Human_SNP_ID_229366000 m1A Human chr5 - 41925359 41925359 41925359 GGATGGCCGCCTCCAGGCGGCCCCAGTCGCTGAAGGGCGGCGGCGGCGAGTTTGTTCCGCTGCGC GGATGGCCGCCTCCAGGCGGCCCCAGTCGCTGTAGGGCGGCGGCGGCGAGTTTGTTCCGCTGCGC T A HSALNG0041434 RNACentral:URS0000EB3A65 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:41925308..41927015 26863196 MeRIP-seq:(Medium) rs765044998 Functional Loss SNV dbSNP153 33..33 33 - - - 65890 RMVar_ID_65890 Human_SNP_ID_229642644 m1A Human chr5 - 42992955 42992955 42992955 AGATCGCGCCACTGCACTCCAGGCTGGGCGACACGGCGAGACTCTGTCTCAAAACAAAACAAAAG AGATCGCGCCACTGCACTCCAGGCTGGGCGACGCGGCGAGACTCTGTCTCAAAACAAAACAAAAG T C AC008875.3 Ensembl:ENSG00000287263 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:42992846..42992954 26863196 MeRIP-seq:(Medium) rs1326152611 Functional Loss SNV dbSNP153 33..33 33 - - - 65891 RMVar_ID_65891 Human_SNP_ID_229647369 m1A Human chr5 - 43010169 43010169 43010169 GCTCAGTTGAGAAGTGAGGCAGATGTGGCCTCAGAGGGTCTGGCGGATGGCTGCCGGGATCACCG GCTCAGTTGAGAAGTGAGGCAGATGTGGCCTCTGAGGGTCTGGCGGATGGCTGCCGGGATCACCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43010118..43010363 26863196 MeRIP-seq:(Medium) rs755520281 Functional Loss SNV dbSNP153 33..33 33 - - - 65892 RMVar_ID_65892 Human_SNP_ID_229647380 m1A Human chr5 + 43010211 43010211 43010211 TCTGCCTCACTTCTCAACTGAGCCATCTTCCCAGCATAAACAGCCGCTGCTTCCTCCTCCTCCGC TCTGCCTCACTTCTCAACTGAGCCATCTTCCCGGCATAAACAGCCGCTGCTTCCTCCTCCTCCGC A G lnc-ZNF131-11 RNACentral:URS0000D57168 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:43010161..43010285 26863196 MeRIP-seq:(Medium) rs943071089 Functional Loss SNV dbSNP153 33..33 33 - - - 65893 RMVar_ID_65893 Human_SNP_ID_229647381 m1A Human chr5 + 43010211 43010211 43010211 TCTGCCTCACTTCTCAACTGAGCCATCTTCCCAGCATAAACAGCCGCTGCTTCCTCCTCCTCCGC TCTGCCTCACTTCTCAACTGAGCCATCTTCCCTGCATAAACAGCCGCTGCTTCCTCCTCCTCCGC A T lnc-ZNF131-11 RNACentral:URS0000D57168 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:43010161..43010285 26863196 MeRIP-seq:(Medium) rs943071089 Functional Loss SNV dbSNP153 33..33 33 - - - 65894 RMVar_ID_65894 Human_SNP_ID_229647524 m1A Human chr5 - 43010711 43010711 43010711 AGAGGAGGAAAACGTCGAGCAGCCCCAGGTGGATGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTG AGAGGAGGAAAACGTCGAGCAGCCCCAGGTGGGTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43010663..43010762 26863196 MeRIP-seq:(Medium) rs1343661694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24106882 65895 RMVar_ID_65895 Human_SNP_ID_229676950 m1A Human chr5 + 43120973 43120973 43120973 CGAACGCACGTGCGCCAGCGGGGCCCGAGCAGAAGGGGAGCCCCGGCTCTCACGAAGAAAATGGA CGAACGCACGTGCGCCAGCGGGGCCCGAGCAGCAGGGGAGCCCCGGCTCTCACGAAGAAAATGGA A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43120901..43121523 26863196 MeRIP-seq:(Medium) rs1349005517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4832040 65896 RMVar_ID_65896 Human_SNP_ID_229677283 m1A Human chr5 + 43121632 43121632 43121632 AGAGGGAGGGCGGGGGAGGGAGAGGCGACCCGAGAGTCGTTGTGGGTCGCGGGCCGGACCGGGTC AGAGGGAGGGCGGGGGAGGGAGAGGCGACCCGGGAGTCGTTGTGGGTCGCGGGCCGGACCGGGTC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:43121616..43121762;chr5:43121624..43121920 26863196 MeRIP-seq:(Medium) rs1008597626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267014,Human_RBP_ID_4845163,Human_RBP_ID_9335626,Human_RBP_ID_9436662,Human_RBP_ID_18424948,Human_RBP_ID_22680404,Human_RBP_ID_24562059,Human_RBP_ID_27842069 65897 RMVar_ID_65897 Human_SNP_ID_229691116 m1A Human chr5 - 43168391 43168391 43168391 CTCTGGCCATAATGCCCTATTAACAGTGATCCAAACAATTTGTTTCCTCTCATTCCTCTGTGACT CTCTGGCCATAATGCCCTATTAACAGTGATCCCAACAATTTGTTTCCTCTCATTCCTCTGTGACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43168387..43168525 26863196 MeRIP-seq:(Medium) rs1327379094 Functional Loss SNV dbSNP153 33..33 33 - - - 65898 RMVar_ID_65898 Human_SNP_ID_229691197 m1A Human chr5 + 43168755 43168755 43168755 TGCTAGCTCAGTGAGGAATCTTGGAGTCGTCCAAACCAGAATGGGAGGTTGGGTAAAGGCAGTGT TGCTAGCTCAGTGAGGAATCTTGGAGTCGTCCGAACCAGAATGGGAGGTTGGGTAAAGGCAGTGT A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43168707..43168937 26863196 MeRIP-seq:(Medium) rs1410242228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_347795 65899 RMVar_ID_65899 Human_SNP_ID_229726521 m1A Human chr5 + 43298951 43298951 43298951 TCTTTTGGCCAGCAAGCTTCTGCATTCAAAGGAAGTGATCCAGGCATGGTGAAAGAGCTTTAGAA TCTTTTGGCCAGCAAGCTTCTGCATTCAAAGGTAGTGATCCAGGCATGGTGAAAGAGCTTTAGAA A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:43298901..43299060 26863196 MeRIP-seq:(Medium) rs762805859 Functional Loss SNV dbSNP153 33..33 33 - - - 65900 RMVar_ID_65900 Human_SNP_ID_229729775 m1A Human chr5 - 43313408 43313408 43313408 ATAAAGCTGGTGGCGAAGGGGAGGCGCCGCGGACTGTCCTTTCGTGGCTCACTCCCTTTCCTCTG ATAAAGCTGGTGGCGAAGGGGAGGCGCCGCGGCCTGTCCTTTCGTGGCTCACTCCCTTTCCTCTG T G HMGCS1 Ensembl:ENSG00000112972 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43312934..43313413 26863196 MeRIP-seq:(Medium) rs942300594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845686,Human_RBP_ID_8893993,Human_RBP_ID_9306450,Human_RBP_ID_9335212 Human_Splice_Rec_647949,Human_Splice_Rec_647969,Human_Splice_Rec_647991,Human_Splice_Rec_647993 RMVar_hsa_circ_112058,RMVar_hsa_circ_231247,RMVar_hsa_circ_82837,RMVar_hsa_circ_231263 65901 RMVar_ID_65901 Human_SNP_ID_229729780 m1A Human chr5 - 43313419 43313419 43313419 GGTTGGCGGCTATAAAGCTGGTGGCGAAGGGGAGGCGCCGCGGACTGTCCTTTCGTGGCTCACTC GGTTGGCGGCTATAAAGCTGGTGGCGAAGGGGGGGCGCCGCGGACTGTCCTTTCGTGGCTCACTC T C HMGCS1 Ensembl:ENSG00000112972 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr5:43313256..43313452;chr5:43313293..43313418 26863196 MeRIP-seq:(Medium) rs1164252011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845686,Human_RBP_ID_8893993,Human_RBP_ID_9306450,Human_RBP_ID_9335212 Human_Splice_Rec_647949,Human_Splice_Rec_647969,Human_Splice_Rec_647991,Human_Splice_Rec_647993 RMVar_hsa_circ_112058,RMVar_hsa_circ_231247,RMVar_hsa_circ_82837,RMVar_hsa_circ_231263 65902 RMVar_ID_65902 Human_SNP_ID_229772939 m1A Human chr5 - 43483785 43483785 43483785 GTATGGCTGAGCCGCTGCGTGGGACTGAGGGGAGGGGGCCGGGTGGACGCCGCGGAACTGCGTCC GTATGGCTGAGCCGCTGCGTGGGACTGAGGGGTGGGGGCCGGGTGGACGCCGCGGAACTGCGTCC T A TMEM267 Ensembl:ENSG00000151881 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43483523..43483875 26863196 MeRIP-seq:(Medium) rs569799769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250804,Human_RBP_ID_267089,Human_RBP_ID_789341,Human_RBP_ID_5090028,Human_RBP_ID_7441647,Human_RBP_ID_9436847,Human_RBP_ID_23050400 65903 RMVar_ID_65903 Human_SNP_ID_229772940 m1A Human chr5 - 43483785 43483785 43483785 GTATGGCTGAGCCGCTGCGTGGGACTGAGGGGAGGGGGCCGGGTGGACGCCGCGGAACTGCGTCC GTATGGCTGAGCCGCTGCGTGGGACTGAGGGGGGGGGGCCGGGTGGACGCCGCGGAACTGCGTCC T C TMEM267 Ensembl:ENSG00000151881 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43483523..43483875 26863196 MeRIP-seq:(Medium) rs569799769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250804,Human_RBP_ID_267089,Human_RBP_ID_789341,Human_RBP_ID_5090028,Human_RBP_ID_7441647,Human_RBP_ID_9436847,Human_RBP_ID_23050400 65904 RMVar_ID_65904 Human_SNP_ID_229783203 m1A Human chr5 - 43522177 43522137 43522177 CCTCACTTCTCAGACGGGGCAGCCGGGCAGAGACGCTCCTCACCTCCCAGACGGGGTCGCGGCCG CCTCACTTCTCAGACGGGGCAGCCGGGCAGAG_________________________________ CCTCTACCCGGCCGCGACCCCGTCTGGGAGGTGAGGAGCGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43522175..43522284 26863196 MeRIP-seq:(Medium) rs1291476058 Functional Loss DEL dbSNP153 33..65 33 - - - 65905 RMVar_ID_65905 Human_SNP_ID_229792247 m1A Human chr5 - 43555995 43555995 43555995 TGACGCCCCGTTTTTTTTTCTTTTGCAGAGCAAACGAGGCCCCTGAGAGCTCCACCTAGTTCACA TGACGCCCCGTTTTTTTTTCTTTTGCAGAGCAGACGAGGCCCCTGAGAGCTCCACCTAGTTCACA T C PAIP1 Ensembl:ENSG00000172239 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:43555925..43556053;chr5:43555926..43556025 26863196 MeRIP-seq:(Medium) rs1208224586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942800,Human_RBP_ID_4832348,Human_RBP_ID_9341495,Human_RBP_ID_23258882 Human_Splice_Rec_648116,Human_Splice_Rec_648136,Human_Splice_Rec_648158,Human_Splice_Rec_648178,Human_Splice_Rec_648196,Human_Splice_Rec_648214,Human_Splice_Rec_648224 65906 RMVar_ID_65906 Human_SNP_ID_229792336 m1A Human chr5 + 43556213 43556213 43556213 TGTGACTCCGTTATGGGCATACCTGCCTCTCAAATGAGTGCTTGCGAGCTTTTTTCCTCTCTGTC TGTGACTCCGTTATGGGCATACCTGCCTCTCAGATGAGTGCTTGCGAGCTTTTTTCCTCTCTGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:43556211..43556312 32194978 MeRIP-seq:(Medium) rs896703509 Functional Loss SNV dbSNP153 33..33 33 - - - 65907 RMVar_ID_65907 Human_SNP_ID_229792641 m1A Human chr5 - 43556893 43556893 43556893 CCCGCGGCGCCTTCCCCCCGCGTCCTATCGCGAGCGCAGCGGCAGCGGCCCCTGGAGGAGGAGGC CCCGCGGCGCCTTCCCCCCGCGTCCTATCGCGTGCGCAGCGGCAGCGGCCCCTGGAGGAGGAGGC T A PAIP1 Ensembl:ENSG00000172239 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:43556744..43557100 26863196 MeRIP-seq:(Medium) rs1339271635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845690 Human_Splice_Rec_648135,Human_Splice_Rec_648177,Human_Splice_Rec_648231 65908 RMVar_ID_65908 Human_SNP_ID_229792656 m1A Human chr5 + 43556913 43556913 43556913 CTGCCGCTGCGCTCGCGATAGGACGCGGGGGGAAGGCGCCGCGGGTCGGCTATAGCCGCCGCGCC CTGCCGCTGCGCTCGCGATAGGACGCGGGGGGGAGGCGCCGCGGGTCGGCTATAGCCGCCGCGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:43556863..43557063 32194978 MeRIP-seq:(Medium) rs1197399463 Functional Loss SNV dbSNP153 33..33 33 - - - 65909 RMVar_ID_65909 Human_SNP_ID_229792657 m1A Human chr5 + 43556913 43556913 43556913 CTGCCGCTGCGCTCGCGATAGGACGCGGGGGGAAGGCGCCGCGGGTCGGCTATAGCCGCCGCGCC CTGCCGCTGCGCTCGCGATAGGACGCGGGGGGTAGGCGCCGCGGGTCGGCTATAGCCGCCGCGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:43556863..43557063 32194978 MeRIP-seq:(Medium) rs1197399463 Functional Loss SNV dbSNP153 33..33 33 - - - 65910 RMVar_ID_65910 Human_SNP_ID_229792665 m1A Human chr5 + 43556932 43556932 43556932 AGGACGCGGGGGGAAGGCGCCGCGGGTCGGCTATAGCCGCCGCGCCTCACTCGGGCCTCATGGAG AGGACGCGGGGGGAAGGCGCCGCGGGTCGGCTCTAGCCGCCGCGCCTCACTCGGGCCTCATGGAG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:43556740..43557070 26863196 MeRIP-seq:(Medium) rs1290696705 Functional Loss SNV dbSNP153 33..33 33 - - - 65911 RMVar_ID_65911 Human_SNP_ID_229792681 m1A Human chr5 - 43556987 43556987 43556987 CCGTCCGCTCCGCCAGAAGCACCGAGCAGCCGAGCCGGGGCCCGCCGCCCTCCTCCTCCATGAGG CCGTCCGCTCCGCCAGAAGCACCGAGCAGCCGGGCCGGGGCCCGCCGCCCTCCTCCTCCATGAGG T C PAIP1 Ensembl:ENSG00000172239 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr5:43556361..43557359;chr5:43556661..43557093 26863196 MeRIP-seq:(Medium) rs940639233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642788,Human_RBP_ID_4845166,Human_RBP_ID_5242241,Human_RBP_ID_9335216 65912 RMVar_ID_65912 Human_SNP_ID_229792703 m1A Human chr5 + 43557042 43557025 43557042 GAGCGGACGGCAGCCCGAGCACCCGCCGCTCCAGAGCGCCCGCCCCGCTCGGCTACCCTCGGCTT GAGCGGACGGCAGCCC_________________GAGCGCCCGCCCCGCTCGGCTACCCTCGGCTT CGAGCACCCGCCGCTCCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr5:43556701..43557174;chr5:43556361..43557359;chr5:43556211..43557359;chr5:43556876..43557100 26863196 MeRIP-seq:(Medium) rs1208468031 Functional Loss DEL dbSNP153 17..33 33 - - - 65913 RMVar_ID_65913 Human_SNP_ID_229792715 m1A Human chr5 + 43557042 43557042 43557042 GAGCGGACGGCAGCCCGAGCACCCGCCGCTCCAGAGCGCCCGCCCCGCTCGGCTACCCTCGGCTT GAGCGGACGGCAGCCCGAGCACCCGCCGCTCCCGAGCGCCCGCCCCGCTCGGCTACCCTCGGCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr5:43556701..43557174;chr5:43556361..43557359;chr5:43556211..43557359;chr5:43556876..43557100 26863196 MeRIP-seq:(Medium) rs1313076439 Functional Loss SNV dbSNP153 33..33 33 - - - 65914 RMVar_ID_65914 Human_SNP_ID_229792891 m1A Human chr5 + 43557557 43557557 43557557 GAGACTGTCACCTGCTCCGTTAGCATCGGGGGAAGGGAGTAGAAACGGAATCAAAATATGTGTCC GAGACTGTCACCTGCTCCGTTAGCATCGGGGGCAGGGAGTAGAAACGGAATCAAAATATGTGTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:43557508..43557608 26863196 MeRIP-seq:(Medium) rs1270236312 Functional Loss SNV dbSNP153 33..33 33 - - - 65915 RMVar_ID_65915 Human_SNP_ID_229803664 m1A Human chr5 + 43602747 43602747 43602747 GAAGTTCTGATTTTTCCTAGCGAGCTGGAGGAAAGGCAGGTACCCGGAGTGGAGTTATATTACCT GAAGTTCTGATTTTTCCTAGCGAGCTGGAGGACAGGCAGGTACCCGGAGTGGAGTTATATTACCT A C NNT Ensembl:ENSG00000112992 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43602704..43602777 26863196 MeRIP-seq:(Medium) rs1453984862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7442049 Human_Splice_Rec_648267 RMVar_hsa_circ_83824,RMVar_hsa_circ_231271 65916 RMVar_ID_65916 Human_SNP_ID_229803704 m1A Human chr5 - 43602880 43602880 43602880 CGCCAGTCCTTGTCAATCAAACCTGGTGCCAAACGCGGCAGCTGAAGTTTTCAGGGACACATTTG CGCCAGTCCTTGTCAATCAAACCTGGTGCCAATCGCGGCAGCTGAAGTTTTCAGGGACACATTTG T A NNT-AS1 Ensembl:ENSG00000248092 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:43602791..43603128 32194978 MeRIP-seq:(Medium) rs1297794049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3784899,Human_RBP_ID_4847286 Human_miRNA_ID_3149190,Human_miRNA_ID_3163826,Human_miRNA_ID_3216462 65917 RMVar_ID_65917 Human_SNP_ID_229803843 m1A Human chr5 + 43603264 43603264 43603264 CCAGCGCGACGTCCTCTCGCGGCCCTCAGGGCACAGCCCAAGGCTGTCAGCCTCCCGGCCCAGGT CCAGCGCGACGTCCTCTCGCGGCCCTCAGGGCGCAGCCCAAGGCTGTCAGCCTCCCGGCCCAGGT A G NNT Ensembl:ENSG00000112992 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:43603218..43603291 26863196 MeRIP-seq:(Medium) rs1214206126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845694,Human_RBP_ID_8893512 Human_Splice_Rec_648445,Human_Splice_Rec_648465,Human_Splice_Rec_648503,Human_Splice_Rec_648545,Human_Splice_Rec_648587,Human_Splice_Rec_648613,Human_Splice_Rec_648657,Human_Splice_Rec_648697,Human_Splice_Rec_648739 RMVar_hsa_circ_83824,RMVar_hsa_circ_231271 65918 RMVar_ID_65918 Human_SNP_ID_229803885 m1A Human chr5 + 43603399 43603399 43603399 GGCCTTTCCTGAAGACCACGGCCCTCGCCGGGAGAGAGACCTGTCAAAGAGCAAAGCGGGGCGGG GGCCTTTCCTGAAGACCACGGCCCTCGCCGGGGGAGAGACCTGTCAAAGAGCAAAGCGGGGCGGG A G NNT Ensembl:ENSG00000112992 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:43603391..43603488 26863196 MeRIP-seq:(Medium) rs1475199496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_648781 RMVar_hsa_circ_83824,RMVar_hsa_circ_231271 65919 RMVar_ID_65919 Human_SNP_ID_229806173 m1A Human chr5 - 43613038 43613038 43613038 TGATCATCTGAGAACTTGGAAGCTTCGCCCGCACCCGATTCCACGACAACATTAAAACCCTGCTT TGATCATCTGAGAACTTGGAAGCTTCGCCCGCCCCCGATTCCACGACAACATTAAAACCCTGCTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:43612994..43613093 26863196 MeRIP-seq:(Medium) rs1455355441 Functional Loss SNV dbSNP153 33..33 33 - - - 65920 RMVar_ID_65920 Human_SNP_ID_229806190 m1A Human chr5 + 43613098 43613085 43613098 GATCACTATAGAGTGGCAGGTGCCCAAATCCAAGGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT GATCACTATAGAGTGGCAGG_____________GGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT GTGCCCAAATCCAA G NNT Ensembl:ENSG00000112992 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:43613051..43613150 26863196 MeRIP-seq:(Medium) rs775723069 Functional Loss DEL dbSNP153 21..33 33 - - - Human_Splice_Rec_648265,Human_Splice_Rec_648271,Human_Splice_Rec_648279,Human_Splice_Rec_648321,Human_Splice_Rec_648363,Human_Splice_Rec_648407,Human_Splice_Rec_648449,Human_Splice_Rec_648469,Human_Splice_Rec_648507,Human_Splice_Rec_648619,Human_Splice_Rec_648659,Human_Splice_Rec_648701,Human_Splice_Rec_648743,Human_Splice_Rec_648785,Human_Splice_Rec_648827,Human_Splice_Rec_648869,Human_Splice_Rec_648911 RMVar_hsa_circ_49513,RMVar_hsa_circ_83824,RMVar_hsa_circ_289837,RMVar_hsa_circ_322029,RMVar_hsa_circ_366539,RMVar_hsa_circ_231271,RMVar_hsa_circ_369177,RMVar_hsa_circ_359767,RMVar_hsa_circ_309219,RMVar_hsa_circ_314632,RMVar_hsa_circ_295127,RMVar_hsa_circ_74618,RMVar_hsa_circ_85295,RMVar_hsa_circ_231273,RMVar_hsa_circ_231275,RMVar_hsa_circ_231276,RMVar_hsa_circ_231277,RMVar_hsa_circ_231274,RMVar_hsa_circ_81687,RMVar_hsa_circ_332473,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_319291,RMVar_hsa_circ_231278,RMVar_hsa_circ_231279 65921 RMVar_ID_65921 Human_SNP_ID_229806194 m1A Human chr5 + 43613098 43613087 43613098 GATCACTATAGAGTGGCAGGTGCCCAAATCCAAGGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT GATCACTATAGAGTGGCAGGTG___________GGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT GCCCAAATCCAA G NNT Ensembl:ENSG00000112992 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:43613051..43613150 26863196 MeRIP-seq:(Medium) rs760848489 Functional Loss DEL dbSNP153 23..33 33 - - - Human_Splice_Rec_648265,Human_Splice_Rec_648271,Human_Splice_Rec_648279,Human_Splice_Rec_648321,Human_Splice_Rec_648363,Human_Splice_Rec_648407,Human_Splice_Rec_648449,Human_Splice_Rec_648469,Human_Splice_Rec_648507,Human_Splice_Rec_648619,Human_Splice_Rec_648659,Human_Splice_Rec_648701,Human_Splice_Rec_648743,Human_Splice_Rec_648785,Human_Splice_Rec_648827,Human_Splice_Rec_648869,Human_Splice_Rec_648911 RMVar_hsa_circ_49513,RMVar_hsa_circ_83824,RMVar_hsa_circ_289837,RMVar_hsa_circ_322029,RMVar_hsa_circ_366539,RMVar_hsa_circ_231271,RMVar_hsa_circ_369177,RMVar_hsa_circ_359767,RMVar_hsa_circ_309219,RMVar_hsa_circ_314632,RMVar_hsa_circ_295127,RMVar_hsa_circ_74618,RMVar_hsa_circ_85295,RMVar_hsa_circ_231273,RMVar_hsa_circ_231275,RMVar_hsa_circ_231276,RMVar_hsa_circ_231277,RMVar_hsa_circ_231274,RMVar_hsa_circ_81687,RMVar_hsa_circ_332473,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_319291,RMVar_hsa_circ_231278,RMVar_hsa_circ_231279 65922 RMVar_ID_65922 Human_SNP_ID_229806200 m1A Human chr5 + 43613098 43613098 43613098 GATCACTATAGAGTGGCAGGTGCCCAAATCCAAGGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT GATCACTATAGAGTGGCAGGTGCCCAAATCCAGGGGGCAAAGGAAGTGCTGGCTTCTGATTTGGT A G NNT Ensembl:ENSG00000112992 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:43613051..43613150 26863196 MeRIP-seq:(Medium) rs1177951473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_648265,Human_Splice_Rec_648271,Human_Splice_Rec_648279,Human_Splice_Rec_648321,Human_Splice_Rec_648363,Human_Splice_Rec_648407,Human_Splice_Rec_648449,Human_Splice_Rec_648469,Human_Splice_Rec_648507,Human_Splice_Rec_648619,Human_Splice_Rec_648659,Human_Splice_Rec_648701,Human_Splice_Rec_648743,Human_Splice_Rec_648785,Human_Splice_Rec_648827,Human_Splice_Rec_648869,Human_Splice_Rec_648911 RMVar_hsa_circ_49513,RMVar_hsa_circ_83824,RMVar_hsa_circ_289837,RMVar_hsa_circ_322029,RMVar_hsa_circ_366539,RMVar_hsa_circ_231271,RMVar_hsa_circ_369177,RMVar_hsa_circ_359767,RMVar_hsa_circ_309219,RMVar_hsa_circ_314632,RMVar_hsa_circ_295127,RMVar_hsa_circ_74618,RMVar_hsa_circ_85295,RMVar_hsa_circ_231273,RMVar_hsa_circ_231275,RMVar_hsa_circ_231276,RMVar_hsa_circ_231277,RMVar_hsa_circ_231274,RMVar_hsa_circ_81687,RMVar_hsa_circ_332473,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_319291,RMVar_hsa_circ_231278,RMVar_hsa_circ_231279 65923 RMVar_ID_65923 Human_SNP_ID_229809638 m1A Human chr5 + 43628262 43628262 43628262 TGGTGCTGAGCCCTTGGAGGTGGACTTGAAGGAATCTGGTGAGGGACAAGGAGGATATGCAAAAG TGGTGCTGAGCCCTTGGAGGTGGACTTGAAGGCATCTGGTGAGGGACAAGGAGGATATGCAAAAG A C NNT Ensembl:ENSG00000112992 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:43628213..43628329 26863196 MeRIP-seq:(Medium) rs1236008990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8616599,Human_RBP_ID_9349581,Human_RBP_ID_18843185,Human_RBP_ID_23050246,Human_RBP_ID_26350820,Human_RBP_ID_27825377 Human_Splice_Rec_648286,Human_Splice_Rec_648328,Human_Splice_Rec_648370,Human_Splice_Rec_648414,Human_Splice_Rec_648456,Human_Splice_Rec_648472,Human_Splice_Rec_648514,Human_Splice_Rec_648554,Human_Splice_Rec_648598,Human_Splice_Rec_648626,Human_Splice_Rec_648666,Human_Splice_Rec_648706,Human_Splice_Rec_648750,Human_Splice_Rec_648792,Human_Splice_Rec_648834,Human_Splice_Rec_648876,Human_Splice_Rec_648918,Human_Splice_Rec_648954 RMVar_hsa_circ_9463,RMVar_hsa_circ_49513,RMVar_hsa_circ_289837,RMVar_hsa_circ_322029,RMVar_hsa_circ_309219,RMVar_hsa_circ_314632,RMVar_hsa_circ_295127,RMVar_hsa_circ_85295,RMVar_hsa_circ_74448,RMVar_hsa_circ_231273,RMVar_hsa_circ_231275,RMVar_hsa_circ_231276,RMVar_hsa_circ_231277,RMVar_hsa_circ_231274,RMVar_hsa_circ_81687,RMVar_hsa_circ_332473,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_319291,RMVar_hsa_circ_231278,RMVar_hsa_circ_231279,RMVar_hsa_circ_303298,RMVar_hsa_circ_366143,RMVar_hsa_circ_91099,RMVar_hsa_circ_71281,RMVar_hsa_circ_42829,RMVar_hsa_circ_71950,RMVar_hsa_circ_231280,RMVar_hsa_circ_231281,RMVar_hsa_circ_61512,RMVar_hsa_circ_319230,RMVar_hsa_circ_329772,RMVar_hsa_circ_351115,RMVar_hsa_circ_367285,RMVar_hsa_circ_326193,RMVar_hsa_circ_119138,RMVar_hsa_circ_311423,RMVar_hsa_circ_117629,RMVar_hsa_circ_231289,RMVar_hsa_circ_231284,RMVar_hsa_circ_231286,RMVar_hsa_circ_231287,RMVar_hsa_circ_231285,RMVar_hsa_circ_325828,RMVar_hsa_circ_374673,RMVar_hsa_circ_231283,RMVar_hsa_circ_369877,RMVar_hsa_circ_299832,RMVar_hsa_circ_231288 65924 RMVar_ID_65924 Human_SNP_ID_229813117 m1A Human chr5 - 43644792 43644792 43644792 AGGAATAGATCTCTTTACTTACTTTCATCACTACAGTTCCTCTAATGACATGACCCATCGTACCA AGGAATAGATCTCTTTACTTACTTTCATCACTGCAGTTCCTCTAATGACATGACCCATCGTACCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:43644193..43645532 32194978 MeRIP-seq:(Medium) rs201576637 Functional Loss SNV dbSNP153 33..33 33 - - - 65925 RMVar_ID_65925 Human_SNP_ID_229815307 m1A Human chr5 + 43653152 43653152 43653152 GCTGGAGGACTGGCAGCCACCCTCGGAGTCCTAAAACCGGGCCCAGAATTACTAGCTCAGATGTC GCTGGAGGACTGGCAGCCACCCTCGGAGTCCTGAAACCGGGCCCAGAATTACTAGCTCAGATGTC A G NNT Ensembl:ENSG00000112992 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:43653101..43653286 32194978 MeRIP-seq:(Medium) rs147914179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041628,Human_RBP_ID_8893516,Human_RBP_ID_9306969 Human_Splice_Rec_648301,Human_Splice_Rec_648343,Human_Splice_Rec_648385,Human_Splice_Rec_648429,Human_Splice_Rec_648487,Human_Splice_Rec_648529,Human_Splice_Rec_648571,Human_Splice_Rec_648641,Human_Splice_Rec_648681,Human_Splice_Rec_648723,Human_Splice_Rec_648765,Human_Splice_Rec_648807,Human_Splice_Rec_648849,Human_Splice_Rec_648891,Human_Splice_Rec_648933 RMVar_hsa_circ_49513,RMVar_hsa_circ_289837,RMVar_hsa_circ_322029,RMVar_hsa_circ_309219,RMVar_hsa_circ_85295,RMVar_hsa_circ_74448,RMVar_hsa_circ_231273,RMVar_hsa_circ_231275,RMVar_hsa_circ_231274,RMVar_hsa_circ_81687,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_231279,RMVar_hsa_circ_91099,RMVar_hsa_circ_71281,RMVar_hsa_circ_78636,RMVar_hsa_circ_71950,RMVar_hsa_circ_231281,RMVar_hsa_circ_61512,RMVar_hsa_circ_319230,RMVar_hsa_circ_351115,RMVar_hsa_circ_367285,RMVar_hsa_circ_311423,RMVar_hsa_circ_122177,RMVar_hsa_circ_231286,RMVar_hsa_circ_231287,RMVar_hsa_circ_374673,RMVar_hsa_circ_299832,RMVar_hsa_circ_332935,RMVar_hsa_circ_231288,RMVar_hsa_circ_312704,RMVar_hsa_circ_231291,RMVar_hsa_circ_26928,RMVar_hsa_circ_54793,RMVar_hsa_circ_231292,RMVar_hsa_circ_231293,RMVar_hsa_circ_88046,RMVar_hsa_circ_113924,RMVar_hsa_circ_231295,RMVar_hsa_circ_231296,RMVar_hsa_circ_105580,RMVar_hsa_circ_231297,RMVar_hsa_circ_266709,RMVar_hsa_circ_231298 65926 RMVar_ID_65926 Human_SNP_ID_229821813 m1A Human chr5 + 43677348 43677348 43677348 TAGAGAAAGAATAATAACAAAGTTAGGCTGGGACAGGGGACCGCAGTGTCGTCAAAGCCAAGTAT TAGAGAAAGAATAATAACAAAGTTAGGCTGGGGCAGGGGACCGCAGTGTCGTCAAAGCCAAGTAT A G NNT Ensembl:ENSG00000112992 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43677335..43677453 26863196 MeRIP-seq:(Medium) rs13186083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15454919 RMVar_hsa_circ_289837,RMVar_hsa_circ_85295,RMVar_hsa_circ_74448,RMVar_hsa_circ_231273,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_91099,RMVar_hsa_circ_78636,RMVar_hsa_circ_71950,RMVar_hsa_circ_231281,RMVar_hsa_circ_61512,RMVar_hsa_circ_319230,RMVar_hsa_circ_231287,RMVar_hsa_circ_299832,RMVar_hsa_circ_332935,RMVar_hsa_circ_231293,RMVar_hsa_circ_88046,RMVar_hsa_circ_231295,RMVar_hsa_circ_231296,RMVar_hsa_circ_105580,RMVar_hsa_circ_231298,RMVar_hsa_circ_314135,RMVar_hsa_circ_231300,RMVar_hsa_circ_231306,RMVar_hsa_circ_268014,RMVar_hsa_circ_302874,RMVar_hsa_circ_378580,RMVar_hsa_circ_363516,RMVar_hsa_circ_301084,RMVar_hsa_circ_231307,RMVar_hsa_circ_231304,RMVar_hsa_circ_231305,RMVar_hsa_circ_231303 65927 RMVar_ID_65927 Human_SNP_ID_229821814 m1A Human chr5 + 43677348 43677348 43677348 TAGAGAAAGAATAATAACAAAGTTAGGCTGGGACAGGGGACCGCAGTGTCGTCAAAGCCAAGTAT TAGAGAAAGAATAATAACAAAGTTAGGCTGGGTCAGGGGACCGCAGTGTCGTCAAAGCCAAGTAT A T NNT Ensembl:ENSG00000112992 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43677335..43677453 26863196 MeRIP-seq:(Medium) rs13186083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15454919 RMVar_hsa_circ_289837,RMVar_hsa_circ_85295,RMVar_hsa_circ_74448,RMVar_hsa_circ_231273,RMVar_hsa_circ_231272,RMVar_hsa_circ_344251,RMVar_hsa_circ_91099,RMVar_hsa_circ_78636,RMVar_hsa_circ_71950,RMVar_hsa_circ_231281,RMVar_hsa_circ_61512,RMVar_hsa_circ_319230,RMVar_hsa_circ_231287,RMVar_hsa_circ_299832,RMVar_hsa_circ_332935,RMVar_hsa_circ_231293,RMVar_hsa_circ_88046,RMVar_hsa_circ_231295,RMVar_hsa_circ_231296,RMVar_hsa_circ_105580,RMVar_hsa_circ_231298,RMVar_hsa_circ_314135,RMVar_hsa_circ_231300,RMVar_hsa_circ_231306,RMVar_hsa_circ_268014,RMVar_hsa_circ_302874,RMVar_hsa_circ_378580,RMVar_hsa_circ_363516,RMVar_hsa_circ_301084,RMVar_hsa_circ_231307,RMVar_hsa_circ_231304,RMVar_hsa_circ_231305,RMVar_hsa_circ_231303 65928 RMVar_ID_65928 Human_SNP_ID_230140979 m1A Human chr5 - 44809001 44809001 44809001 GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGACCGCGTAGCAAAGGCCTCCAACACCTGGCCGC GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGGCCGCGTAGCAAAGGCCTCCAACACCTGGCCGC T C MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:44808951..44809846;chr5:44808951..44809355;chr5:44808951..44809133;chr5:44808951..44809180 26863196 MeRIP-seq:(Medium) rs963177485 Functional Loss SNV dbSNP153 33..33 33 - - - 65929 RMVar_ID_65929 Human_SNP_ID_230140980 m1A Human chr5 - 44809001 44809001 44809001 GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGACCGCGTAGCAAAGGCCTCCAACACCTGGCCGC GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGCCCGCGTAGCAAAGGCCTCCAACACCTGGCCGC T G MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:44808951..44809846;chr5:44808951..44809355;chr5:44808951..44809133;chr5:44808951..44809180 26863196 MeRIP-seq:(Medium) rs963177485 Functional Loss SNV dbSNP153 33..33 33 - - - 65930 RMVar_ID_65930 Human_SNP_ID_230140989 m1A Human chr5 - 44809011 44809011 44809011 CGTGGCGGCGGCATTAGCCGCGGTGTGCAATGAAAGCCTCGGACCGCGTAGCAAAGGCCTCCAAC CGTGGCGGCGGCATTAGCCGCGGTGTGCAATGGAAGCCTCGGACCGCGTAGCAAAGGCCTCCAAC T C MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:44808951..44809171 26863196 MeRIP-seq:(Medium) rs775553861 Functional Loss SNV dbSNP153 33..33 33 - - - 65931 RMVar_ID_65931 Human_SNP_ID_230140993 m1A Human chr5 + 44809018 44809018 44809018 GCCTTTGCTACGCGGTCCGAGGCTTTCATTGCACACCGCGGCTAATGCCGCCGCCACGGCTACAG GCCTTTGCTACGCGGTCCGAGGCTTTCATTGCGCACCGCGGCTAATGCCGCCGCCACGGCTACAG A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:44808951..44809125 26863196 MeRIP-seq:(Medium) rs764017230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77519,Human_RBP_ID_1654967,Human_RBP_ID_4845696,Human_RBP_ID_8890274,Human_RBP_ID_9306455,Human_RBP_ID_22099394 65932 RMVar_ID_65932 Human_SNP_ID_230141040 m1A Human chr5 - 44809084 44809084 44809084 TCATGGAGGCCACAATCGGCGGGTACCGCGCGACGGGGGTCGCCGCGACGTCTTGGCAGGTCGTT TCATGGAGGCCACAATCGGCGGGTACCGCGCGTCGGGGGTCGCCGCGACGTCTTGGCAGGTCGTT T A MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:44808951..44809143 26863196 MeRIP-seq:(Medium) rs762071837 Functional Loss SNV dbSNP153 33..33 33 - - - 65933 RMVar_ID_65933 Human_SNP_ID_230141136 m1A Human chr5 + 44809227 44809227 44809227 AGAAGCTGCGAATCCTCACCAAGATGCAGTTTATGAAGTACATGGTTTACCCGCAGACCTTCGCG AGAAGCTGCGAATCCTCACCAAGATGCAGTTTGTGAAGTACATGGTTTACCCGCAGACCTTCGCG A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:44809176..44809250 26863196 MeRIP-seq:(Medium) rs1313881154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_312815,Human_RBP_ID_642890,Human_RBP_ID_1041636,Human_RBP_ID_1654969,Human_RBP_ID_1995829,Human_RBP_ID_4855525,Human_RBP_ID_8890275,Human_RBP_ID_9305829,Human_RBP_ID_18843245,Human_RBP_ID_26826267,Human_RBP_ID_27516134,Human_RBP_ID_27741015 65934 RMVar_ID_65934 Human_SNP_ID_230141222 m1A Human chr5 + 44809352 44809346 44809352 CCGCCCCCAGCGGAGCCCGAGCCCGAGCCCGAACCCGAACCTGAACCTGCGCTGGACCTCGCGGC CCGCCCCCAGCGGAGCCCGAGCCCGAG______CCCGAACCTGAACCTGCGCTGGACCTCGCGGC GCCCGAA G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:44809272..44809447 26863196 MeRIP-seq:(Medium) rs753431420 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_22458840,Human_RBP_ID_27516136 65935 RMVar_ID_65935 Human_SNP_ID_230141230 m1A Human chr5 + 44809352 44809352 44809352 CCGCCCCCAGCGGAGCCCGAGCCCGAGCCCGAACCCGAACCTGAACCTGCGCTGGACCTCGCGGC CCGCCCCCAGCGGAGCCCGAGCCCGAGCCCGAGCCCGAACCTGAACCTGCGCTGGACCTCGCGGC A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:44809272..44809447 26863196 MeRIP-seq:(Medium) rs142383960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22458840,Human_RBP_ID_27516136 65936 RMVar_ID_65936 Human_SNP_ID_230141341 m1A Human chr5 - 44809522 44809519 44809522 CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGGAGGCCCACGAGGGTTGACACCAGCTGATCCAGG CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGG___CCCACGAGGGTTGACACCAGCTGATCCAGG GCCT G MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10,MRPS30-DT:11 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5D30C,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:44809476..44809525 26863196 MeRIP-seq:(Medium) rs753177574 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_231310 65937 RMVar_ID_65937 Human_SNP_ID_230141344 m1A Human chr5 - 44809522 44809522 44809522 CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGGAGGCCCACGAGGGTTGACACCAGCTGATCCAGG CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGGGGGCCCACGAGGGTTGACACCAGCTGATCCAGG T C MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10,MRPS30-DT:11 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5D30C,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:44809476..44809525 26863196 MeRIP-seq:(Medium) rs144926318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231310 65938 RMVar_ID_65938 Human_SNP_ID_230141345 m1A Human chr5 - 44809522 44809522 44809522 CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGGAGGCCCACGAGGGTTGACACCAGCTGATCCAGG CAGCGGCCAGGGCCGGGTTGTGTGGGCTGAGGCGGCCCACGAGGGTTGACACCAGCTGATCCAGG T G MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10,MRPS30-DT:11 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5D30C,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:44809476..44809525 26863196 MeRIP-seq:(Medium) rs144926318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231310 65939 RMVar_ID_65939 Human_SNP_ID_230141778 m1A Human chr5 + 44811012 44811012 44811012 GAAAAAAATTTTGAATATCTTTTTGATAGATTATAGATGCCCAGTTCATTTTTACTGGGTGCGTG GAAAAAAATTTTGAATATCTTTTTGATAGATTGTAGATGCCCAGTTCATTTTTACTGGGTGCGTG A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:44811010..44811919 32194978 MeRIP-seq:(Medium) rs971764392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041640,Human_RBP_ID_1654978,Human_RBP_ID_18048906,Human_RBP_ID_24107361,Human_RBP_ID_27741016 Human_Splice_Rec_649050,Human_Splice_Rec_649058 RMVar_hsa_circ_231311,RMVar_hsa_circ_372380 65940 RMVar_ID_65940 Human_SNP_ID_230141779 m1A Human chr5 + 44811012 44811012 44811012 GAAAAAAATTTTGAATATCTTTTTGATAGATTATAGATGCCCAGTTCATTTTTACTGGGTGCGTG GAAAAAAATTTTGAATATCTTTTTGATAGATTTTAGATGCCCAGTTCATTTTTACTGGGTGCGTG A T MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:44811010..44811919 32194978 MeRIP-seq:(Medium) rs971764392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041640,Human_RBP_ID_1654978,Human_RBP_ID_18048906,Human_RBP_ID_24107361,Human_RBP_ID_27741016 Human_Splice_Rec_649050,Human_Splice_Rec_649058 RMVar_hsa_circ_231311,RMVar_hsa_circ_372380 65941 RMVar_ID_65941 Human_SNP_ID_614242608 m1A Human chr16 - 90006361 90006361 90006361 AGCGGCAGGCCACAGTCCTGGACACGTTTCTCACTGTGGAGAGGCCCCAGGAGGACTAGACCATC AGCGGCAGGCCACAGTCCTGGACACGTTTCTCGCTGTGGAGAGGCCCCAGGAGGACTAGACCATC T C DBNDD1 Ensembl:ENSG00000003249 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:90006311..90006512 32194978 MeRIP-seq:(Medium) rs942081363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103372,RMVar_hsa_circ_110220,RMVar_hsa_circ_180868,RMVar_hsa_circ_180869 65942 RMVar_ID_65942 Human_SNP_ID_614243776 m1A Human chr16 - 90009374 90009374 90009374 CGCAGGCTGCGCTGGGCGTCCCAGCCCAGGGGACAGGGGACAATGGCCACACGCCTGTGGAGGAG CGCAGGCTGCGCTGGGCGTCCCAGCCCAGGGGTCAGGGGACAATGGCCACACGCCTGTGGAGGAG T A DBNDD1 Ensembl:ENSG00000003249 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:90009323..90009433 26863196 MeRIP-seq:(Medium) rs761928446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890104,Human_RBP_ID_4392160 Human_Splice_Rec_1755276,Human_Splice_Rec_1755277,Human_Splice_Rec_1755281,Human_Splice_Rec_1755286,Human_Splice_Rec_1755287,Human_Splice_Rec_1755292,Human_Splice_Rec_1755293,Human_Splice_Rec_1755299 RMVar_hsa_circ_103372,RMVar_hsa_circ_180869 65943 RMVar_ID_65943 Human_SNP_ID_614246899 m1A Human chr16 - 90019286 90019286 90019286 CACCGGAGGTGAGTTCAGCCCCAGCCCCCGAGACCCCCGCGCAGCGCTTCCCCGCAGCGAGCCGC CACCGGAGGTGAGTTCAGCCCCAGCCCCCGAGCCCCCCGCGCAGCGCTTCCCCGCAGCGAGCCGC T G DBNDD1 Ensembl:ENSG00000003249 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:90019281..90019409 26863196 MeRIP-seq:(Medium) rs1041347357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19075668 65944 RMVar_ID_65944 Human_SNP_ID_614248061 m1A Human chr16 - 90022715 90022715 90022715 GCCCCGCTCCCGCCCCTGCTCACCATGACGCCAGCGGACAGGCCCAGCGGCGACTCCGGGACCAG GCCCCGCTCCCGCCCCTGCTCACCATGACGCCTGCGGACAGGCCCAGCGGCGACTCCGGGACCAG T A lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:90022691..90022822 26863196 MeRIP-seq:(Medium) rs80287915 Functional Loss SNV dbSNP153 33..33 33 - - - 65945 RMVar_ID_65945 Human_SNP_ID_614248062 m1A Human chr16 - 90022715 90022715 90022715 GCCCCGCTCCCGCCCCTGCTCACCATGACGCCAGCGGACAGGCCCAGCGGCGACTCCGGGACCAG GCCCCGCTCCCGCCCCTGCTCACCATGACGCCGGCGGACAGGCCCAGCGGCGACTCCGGGACCAG T C lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:90022691..90022822 26863196 MeRIP-seq:(Medium) rs80287915 Functional Loss SNV dbSNP153 33..33 33 - - - 65946 RMVar_ID_65946 Human_SNP_ID_614248063 m1A Human chr16 - 90022715 90022715 90022715 GCCCCGCTCCCGCCCCTGCTCACCATGACGCCAGCGGACAGGCCCAGCGGCGACTCCGGGACCAG GCCCCGCTCCCGCCCCTGCTCACCATGACGCCCGCGGACAGGCCCAGCGGCGACTCCGGGACCAG T G lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:90022691..90022822 26863196 MeRIP-seq:(Medium) rs80287915 Functional Loss SNV dbSNP153 33..33 33 - - - 65947 RMVar_ID_65947 Human_SNP_ID_614248068 m1A Human chr16 - 90022720 90022720 90022720 CCCCAGCCCCGCTCCCGCCCCTGCTCACCATGACGCCAGCGGACAGGCCCAGCGGCGACTCCGGG CCCCAGCCCCGCTCCCGCCCCTGCTCACCATGGCGCCAGCGGACAGGCCCAGCGGCGACTCCGGG T C lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:90022708..90022783 26863196 MeRIP-seq:(Medium) rs1355602289 Functional Loss SNV dbSNP153 33..33 33 - - - 65948 RMVar_ID_65948 Human_SNP_ID_614248069 m1A Human chr16 + 90022722 90022722 90022722 CGGAGTCGCCGCTGGGCCTGTCCGCTGGCGTCATGGTGAGCAGGGGCGGGAGCGGGGCTGGGGTC CGGAGTCGCCGCTGGGCCTGTCCGCTGGCGTCTTGGTGAGCAGGGGCGGGAGCGGGGCTGGGGTC A T GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:90022690..90022799 26863196 MeRIP-seq:(Medium) rs1057484078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419344,Human_RBP_ID_19075670 Human_Splice_Rec_1755359,Human_Splice_Rec_1755379,Human_Splice_Rec_1755389,Human_Splice_Rec_1755405,Human_Splice_Rec_1755407,Human_Splice_Rec_1755427,Human_Splice_Rec_1755435 65949 RMVar_ID_65949 Human_SNP_ID_614250374 m1A Human chr16 + 90029176 90029174 90029177 GGCAGCCTACGGGGCAGGCTACGGGGCAGCTTACGGGGCAGGCTATGGGGCAGCCTACGGGGCAG GGCAGCCTACGGGGCAGGCTACGGGGCAGCT___GGGGCAGGCTATGGGGCAGCCTACGGGGCAG TTAC T GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:90029174..90029319 26863196 MeRIP-seq:(Medium) rs762428710 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_365495 65950 RMVar_ID_65950 Human_SNP_ID_614250379 m1A Human chr16 + 90029176 90029176 90029176 GGCAGCCTACGGGGCAGGCTACGGGGCAGCTTACGGGGCAGGCTATGGGGCAGCCTACGGGGCAG GGCAGCCTACGGGGCAGGCTACGGGGCAGCTTCCGGGGCAGGCTATGGGGCAGCCTACGGGGCAG A C GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:90029174..90029319 26863196 MeRIP-seq:(Medium) rs539417855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365495 65951 RMVar_ID_65951 Human_SNP_ID_614251250 m1A Human chr16 + 90031425 90031422 90031425 TCTGGGAGATCACACGGAGGCAGCTGGAGGAGAAGAAGGCTGAGCTGCGGAACAAAGACCGGGAG TCTGGGAGATCACACGGAGGCAGCTGGAGG___AGAAGGCTGAGCTGCGGAACAAAGACCGGGAG GAGA G GAS8 Ensembl:ENSG00000141013 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:90031198..90031447 32194978 MeRIP-seq:(Medium) rs775350365 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_234919,Human_RBP_ID_892990,Human_RBP_ID_9373492,Human_RBP_ID_12864737,Human_RBP_ID_18984645,Human_RBP_ID_26329519,Human_RBP_ID_27811387 Human_Splice_Rec_1755321,Human_Splice_Rec_1755341,Human_Splice_Rec_1755351,Human_Splice_Rec_1755357,Human_Splice_Rec_1755363,Human_Splice_Rec_1755383,Human_Splice_Rec_1755391,Human_Splice_Rec_1755411,Human_Splice_Rec_1755431,Human_Splice_Rec_1755439,Human_Splice_Rec_1755455 RMVar_hsa_circ_17849,RMVar_hsa_circ_48313,RMVar_hsa_circ_365495,RMVar_hsa_circ_306410,RMVar_hsa_circ_180871,RMVar_hsa_circ_319444,RMVar_hsa_circ_180872,RMVar_hsa_circ_350693 65952 RMVar_ID_65952 Human_SNP_ID_614251252 m1A Human chr16 + 90031425 90031425 90031425 TCTGGGAGATCACACGGAGGCAGCTGGAGGAGAAGAAGGCTGAGCTGCGGAACAAAGACCGGGAG TCTGGGAGATCACACGGAGGCAGCTGGAGGAGGAGAAGGCTGAGCTGCGGAACAAAGACCGGGAG A G GAS8 Ensembl:ENSG00000141013 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:90031198..90031447 32194978 MeRIP-seq:(Medium) rs535600776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234919,Human_RBP_ID_892990,Human_RBP_ID_9373492,Human_RBP_ID_12864737,Human_RBP_ID_18984645,Human_RBP_ID_26329519,Human_RBP_ID_27811387 Human_Splice_Rec_1755321,Human_Splice_Rec_1755341,Human_Splice_Rec_1755351,Human_Splice_Rec_1755357,Human_Splice_Rec_1755363,Human_Splice_Rec_1755383,Human_Splice_Rec_1755391,Human_Splice_Rec_1755411,Human_Splice_Rec_1755431,Human_Splice_Rec_1755439,Human_Splice_Rec_1755455 RMVar_hsa_circ_17849,RMVar_hsa_circ_48313,RMVar_hsa_circ_365495,RMVar_hsa_circ_306410,RMVar_hsa_circ_180871,RMVar_hsa_circ_319444,RMVar_hsa_circ_180872,RMVar_hsa_circ_350693 65953 RMVar_ID_65953 Human_SNP_ID_614251282 m1A Human chr16 + 90031471 90031471 90031471 GCGGAACAAAGACCGGGAGATGGAAGAAGCCGAGGAGAGGCACCAGGTGGAGATCAAGGTGAGTG GCGGAACAAAGACCGGGAGATGGAAGAAGCCGGGGAGAGGCACCAGGTGGAGATCAAGGTGAGTG A G GAS8 Ensembl:ENSG00000141013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:90031194..90035671 26863196 MeRIP-seq:(Medium) rs1490528479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892990,Human_RBP_ID_9373492,Human_RBP_ID_18984645,Human_RBP_ID_26329519,Human_RBP_ID_27811387 Human_Splice_Rec_1755321,Human_Splice_Rec_1755341,Human_Splice_Rec_1755351,Human_Splice_Rec_1755357,Human_Splice_Rec_1755363,Human_Splice_Rec_1755383,Human_Splice_Rec_1755391,Human_Splice_Rec_1755411,Human_Splice_Rec_1755431,Human_Splice_Rec_1755439,Human_Splice_Rec_1755455 RMVar_hsa_circ_17849,RMVar_hsa_circ_48313,RMVar_hsa_circ_365495,RMVar_hsa_circ_306410,RMVar_hsa_circ_180871,RMVar_hsa_circ_319444,RMVar_hsa_circ_180872,RMVar_hsa_circ_350693 65954 RMVar_ID_65954 Human_SNP_ID_614251734 m1A Human chr16 - 90032806 90032805 90032806 CACTCTCCTGTATGCGGTGCTCTTTCTGTGCCAGCTTCATGACTACAGTGCCCTCAGCCTTCATC CACTCTCCTGTATGCGGTGCTCTTTCTGTGCC_GCTTCATGACTACAGTGCCCTCAGCCTTCATC CT C lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:90031248..90035765 26863196 MeRIP-seq:(Medium) rs1343719753 Functional Loss DEL dbSNP153 33..33 33 - - - 65955 RMVar_ID_65955 Human_SNP_ID_614251763 m1A Human chr16 + 90032861 90032861 90032861 CAGGAGAGTGTGCTGCGCAAGGACATGCGGGCACTGAAGGTGGAGCTCAAGGAGCAGGAGCTGGC CAGGAGAGTGTGCTGCGCAAGGACATGCGGGCGCTGAAGGTGGAGCTCAAGGAGCAGGAGCTGGC A G GAS8 Ensembl:ENSG00000141013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:90032675..90032964 26863196 MeRIP-seq:(Medium) rs766295231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12864748,Human_RBP_ID_18987478,Human_RBP_ID_22498653,Human_RBP_ID_22945213,Human_RBP_ID_26330465,Human_RBP_ID_27811388 Human_Splice_Rec_1755323,Human_Splice_Rec_1755365,Human_Splice_Rec_1755385,Human_Splice_Rec_1755393,Human_Splice_Rec_1755413,Human_Splice_Rec_1755433,Human_Splice_Rec_1755441,Human_Splice_Rec_1755457 RMVar_hsa_circ_17849,RMVar_hsa_circ_48313,RMVar_hsa_circ_365495,RMVar_hsa_circ_306410,RMVar_hsa_circ_180871,RMVar_hsa_circ_319444,RMVar_hsa_circ_180872,RMVar_hsa_circ_350693 65956 RMVar_ID_65956 Human_SNP_ID_614252817 m1A Human chr16 - 90036344 90036344 90036344 AAGGCAGCAGCAAACAGCAGCTTAGCAGAGGAAGACGTGGTGCCCCTACGGCTACAGAACATGGA AAGGCAGCAGCAAACAGCAGCTTAGCAGAGGAGGACGTGGTGCCCCTACGGCTACAGAACATGGA T C lnc-DBNDD1-2 RNACentral:URS0000D6E16E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:90036341..90036530 26863196 MeRIP-seq:(Medium) rs745311837 Functional Loss SNV dbSNP153 33..33 33 - - - 65957 RMVar_ID_65957 Human_SNP_ID_614255908 m1A Human chr16 - 90044328 90044327 90044329 AGCTCCCAAAAGAAAGGTGTCCAGGCAGCAATAGACTCTACGAGGACACACCCGTCACTCACCTG AGCTCCCAAAAGAAAGGTGTCCAGGCAGCAA__GACTCTACGAGGACACACCCGTCACTCACCTG CTA C URAHP Ensembl:ENSG00000222019 Pseudogene intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:90044278..90044379 32194978 MeRIP-seq:(Medium) rs1031312622 Functional Loss DEL dbSNP153 32..33 33 - - - 65958 RMVar_ID_65958 Human_SNP_ID_614282796 m1A Human chr16 + 90168752 90168752 90168752 GGACAGAGGTCAGCGTGAGCCCCTTGCCTCACACCGGCCCCTCCCACGCTGAGAGAGGTCAGTGT GGACAGAGGTCAGCGTGAGCCCCTTGCCTCACCCCGGCCCCTCCCACGCTGAGAGAGGTCAGTGT A C FAM157C Ensembl:ENSG00000260528 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62053666 Functional Loss SNV dbSNP153 33..33 33 - - - 65959 RMVar_ID_65959 Human_SNP_ID_614283452 m1A Human chr16 + 90170888 90170888 90170888 GGCAACAGCGGGGTCTGCAGACGCCCTTCTCCAGCCGGAGCTGGGACTGTTCAGTCACTGGGAGA GGCAACAGCGGGGTCTGCAGACGCCCTTCTCCGGCCGGAGCTGGGACTGTTCAGTCACTGGGAGA A G FAM157C Ensembl:ENSG00000260528 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs913121165 Functional Loss SNV dbSNP153 33..33 33 - - - 65960 RMVar_ID_65960 Human_SNP_ID_614283534 m1A Human chr16 + 90171124 90171124 90171124 ACTTGCAGCCTCCCGGCGCCCCCTCCGGGCCCAGCTCTTCCTCCCGGCTGCATCTCCAGGGCGGA ACTTGCAGCCTCCCGGCGCCCCCTCCGGGCCCGGCTCTTCCTCCCGGCTGCATCTCCAGGGCGGA A G FAM157C Ensembl:ENSG00000260528 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1257104604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8188483,Human_RBP_ID_17563898,Human_RBP_ID_22715626 65961 RMVar_ID_65961 Human_SNP_ID_19071992 m1A Human chr1 - 75724812 75724812 75724812 CCACCGCACCGCTGGGCTCCCTCTCACCCTGCAGCATCGCCCGAACCCCGCTGCCATGTTGGCTC CCACCGCACCGCTGGGCTCCCTCTCACCCTGCGGCATCGCCCGAACCCCGCTGCCATGTTGGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:75724726..75724966 26863196 MeRIP-seq:(Medium) rs769935756 Functional Loss SNV dbSNP153 33..33 33 - - - 65962 RMVar_ID_65962 Human_SNP_ID_19071995 m1A Human chr1 - 75724819 75724819 75724819 TCCAGCCCCACCGCACCGCTGGGCTCCCTCTCACCCTGCAGCATCGCCCGAACCCCGCTGCCATG TCCAGCCCCACCGCACCGCTGGGCTCCCTCTCGCCCTGCAGCATCGCCCGAACCCCGCTGCCATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:75724726..75724938 26863196 MeRIP-seq:(Medium) rs768596219 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_264 65963 RMVar_ID_65963 Human_SNP_ID_19071996 m1A Human chr1 - 75724819 75724819 75724819 TCCAGCCCCACCGCACCGCTGGGCTCCCTCTCACCCTGCAGCATCGCCCGAACCCCGCTGCCATG TCCAGCCCCACCGCACCGCTGGGCTCCCTCTCCCCCTGCAGCATCGCCCGAACCCCGCTGCCATG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:75724726..75724938 26863196 MeRIP-seq:(Medium) rs768596219 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_264 65964 RMVar_ID_65964 Human_SNP_ID_19072970 m1A Human chr1 + 75728426 75728426 75728426 TTTACAGGTCCTGAGAAGTATTTCTCGTTTTCATTGGAGATCACAGCATACAAAAGCCAATCGAC TTTACAGGTCCTGAGAAGTATTTCTCGTTTTCGTTGGAGATCACAGCATACAAAAGCCAATCGAC A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:75728401..75728475 26863196 MeRIP-seq:(Medium) rs1446893994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4076864,Human_RBP_ID_5863177,Human_RBP_ID_26869289 Human_Splice_Rec_87246,Human_Splice_Rec_87247,Human_Splice_Rec_87286,Human_Splice_Rec_87287,Human_Splice_Rec_87294,Human_Splice_Rec_87295,Human_Splice_Rec_87308,Human_Splice_Rec_87309,Human_Splice_Rec_87332,Human_Splice_Rec_87333,Human_Splice_Rec_87354,Human_Splice_Rec_87355,Human_Splice_Rec_87360,Human_Splice_Rec_87361,Human_Splice_Rec_87368,Human_Splice_Rec_87369,Human_Splice_Rec_87404,Human_Splice_Rec_87405 Human_miRNA_ID_2787646,Human_miRNA_ID_2817258 RMVar_hsa_circ_50514,RMVar_hsa_circ_60227,RMVar_hsa_circ_133983,RMVar_hsa_circ_66379,RMVar_hsa_circ_278267,RMVar_hsa_circ_289853,RMVar_hsa_circ_298428,RMVar_hsa_circ_278849,RMVar_hsa_circ_79797,RMVar_hsa_circ_133985,RMVar_hsa_circ_133986,RMVar_hsa_circ_133984,RMVar_hsa_circ_133981,RMVar_hsa_circ_133982 65965 RMVar_ID_65965 Human_SNP_ID_19077136 m1A Human chr1 - 75743072 75743072 75743072 CCTAGTGCTGGTATACTATAGAGAAACCCCCGAGGACCATGTGATTAAGTTCCTATCTTTTGAAA CCTAGTGCTGGTATACTATAGAGAAACCCCCGGGGACCATGTGATTAAGTTCCTATCTTTTGAAA T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755963300 Functional Loss SNV dbSNP153 33..33 33 - - - 65966 RMVar_ID_65966 Human_SNP_ID_19303397 m1A Human chr1 + 76700050 76700050 76700050 GGGAGATCAGCCCTGGCATGATCAAAGACTGCAGAGCCACGTGGGTGGTCCTGGGGCACTCAGAG GGGAGATCAGCCCTGGCATGATCAAAGACTGCGGAGCCACGTGGGTGGTCCTGGGGCACTCAGAG A G TPI1P1 Ensembl:ENSG00000226415 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs542567612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5156203,Human_RBP_ID_17456893,Human_RBP_ID_26391190 Human_miRNA_ID_1855418,Human_miRNA_ID_1908254 65967 RMVar_ID_65967 Human_SNP_ID_19303466 m1A Human chr1 + 76700333 76700333 76700333 TGGTACTGGCAAGACTGCAACACCCCAACAGGACCAGGAAGTACACGACAAGCTCCGAGGATGGC TGGTACTGGCAAGACTGCAACACCCCAACAGGCCCAGGAAGTACACGACAAGCTCCGAGGATGGC A C TPI1P1 Ensembl:ENSG00000226415 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs189389208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8979975 65968 RMVar_ID_65968 Human_SNP_ID_19407406 m1A Human chr1 + 77129238 77129238 77129238 AACTGCTCAGGCCATCAAGGGTATGCATATACAAAAAGCCACGAAGTATCTGAAAGATGTCACTT AACTGCTCAGGCCATCAAGGGTATGCATATACGAAAAGCCACGAAGTATCTGAAAGATGTCACTT A G AC113935.1 Ensembl:ENSG00000226084 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs762104922 Functional Loss SNV dbSNP153 33..33 33 - - - 65969 RMVar_ID_65969 Human_SNP_ID_19526571 m1A Human chr1 + 77641652 77641652 77641652 ATTTATTTATATGGTTGTACTAGAATAACTTGATATCTGTGAAGAGAAACCATAATATAGTCACT ATTTATTTATATGGTTGTACTAGAATAACTTGGTATCTGTGAAGAGAAACCATAATATAGTCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77641616..77641713 26863196 MeRIP-seq:(Medium) rs1424379822 Functional Loss SNV dbSNP153 33..33 33 - - - 65970 RMVar_ID_65970 Human_SNP_ID_19531734 m1A Human chr1 - 77663428 77663428 77663428 GGAAGACTTGACAGGAATGAGTGAAGGAGGGAAGGGGACAGTTGTTTTCAGGTAATGCAGGGCTG GGAAGACTTGACAGGAATGAGTGAAGGAGGGACGGGGACAGTTGTTTTCAGGTAATGCAGGGCTG T G AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77663426..77663491 26863196 MeRIP-seq:(Medium) rs1335870194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5865548 RMVar_hsa_circ_134070 65971 RMVar_ID_65971 Human_SNP_ID_19535628 m1A Human chr1 - 77680305 77680305 77680305 GGTGCAAGAATAGTCAGGCTCATAATAGTTGGAGGACAGCCCGAGTCGGTATTTGAGGCAACTTT GGTGCAAGAATAGTCAGGCTCATAATAGTTGGTGGACAGCCCGAGTCGGTATTTGAGGCAACTTT T A AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77680303..77680492 26863196 MeRIP-seq:(Medium) rs940806448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5865739,Human_RBP_ID_11109924 65972 RMVar_ID_65972 Human_SNP_ID_19535637 m1A Human chr1 + 77680338 77680338 77680338 CCAACTATTATGAGCCTGACTATTCTTGCACCATGGCTCTTGCCTCACTGTCAACCTTCTACATT CCAACTATTATGAGCCTGACTATTCTTGCACCGTGGCTCTTGCCTCACTGTCAACCTTCTACATT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77680334..77680440 26863196 MeRIP-seq:(Medium) rs1224903376 Functional Loss SNV dbSNP153 33..33 33 - - - 65973 RMVar_ID_65973 Human_SNP_ID_19555626 m1A Human chr1 - 77759690 77759689 77759690 AGGAAAAGAGGAGCTTGCGGAGGTGCGGCTGCAGGCCGTTGTTGGTCGAGCTGGCGGGTCCCGCG AGGAAAAGAGGAGCTTGCGGAGGTGCGGCTGC_GGCCGTTGTTGGTCGAGCTGGCGGGTCCCGCG CT C USP33 Ensembl:ENSG00000077254 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:77759626..77759809 26863196 MeRIP-seq:(Medium) rs774717710 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4065780,Human_RBP_ID_8754032,Human_RBP_ID_18415568,Human_RBP_ID_18968547 Human_Splice_Rec_88281,Human_Splice_Rec_88399,Human_Splice_Rec_88451,Human_Splice_Rec_88525,Human_Splice_Rec_88549 65974 RMVar_ID_65974 Human_SNP_ID_19560898 m1A Human chr1 - 77779717 77779705 77779718 CCTGGCCCTGTACCTGGAGCTCCAGGCCAGGTACAGCTGGCCTGCCCACGCCAGCTTCCCAGCTG CCTGGCCCTGTACCTGGAGCTCCAGGCCAGG_____________CCCACGCCAGCTTCCCAGCTG GCAGGCCAGCTGTA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:77779676..77779761 26863196 MeRIP-seq:(Medium) rs1264107609 Functional Loss DEL dbSNP153 32..44 33 - - - 65975 RMVar_ID_65975 Human_SNP_ID_19560915 m1A Human chr1 + 77779729 77779729 77779729 TGGCGTGGGCAGGCCAGCTGTACCTGGCCTGGAGCTCCAGGTACAGGGCCAGGGGCGGGGTGGGG TGGCGTGGGCAGGCCAGCTGTACCTGGCCTGGGGCTCCAGGTACAGGGCCAGGGGCGGGGTGGGG A G MIGA1 Ensembl:ENSG00000180488 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77779680..77780039 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_88575,Human_Splice_Rec_88605,Human_Splice_Rec_88635,Human_Splice_Rec_88663,Human_Splice_Rec_88695,Human_Splice_Rec_88723 65976 RMVar_ID_65976 Human_SNP_ID_19561077 m1A Human chr1 - 77780211 77780211 77780211 TCAAAACCACCCGCATCCAAGCCGAACCTGAGACCTCACCAGCTGCCCTACCTCCAGCGCGCTCT TCAAAACCACCCGCATCCAAGCCGAACCTGAGTCCTCACCAGCTGCCCTACCTCCAGCGCGCTCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77779701..77780289 26863196 MeRIP-seq:(Medium) rs1012088713 Functional Loss SNV dbSNP153 33..33 33 - - - 65977 RMVar_ID_65977 Human_SNP_ID_19586311 m1A Human chr1 - 77885286 77885286 77885286 GTAAATATCTGGAGAAGCAAATATTTGGAGGAAGAGTGGTCCAGGGATAGATACAAAGGCCCAGA GTAAATATCTGGAGAAGCAAATATTTGGAGGAGGAGTGGTCCAGGGATAGATACAAAGGCCCAGA T C NEXN-AS1 Ensembl:ENSG00000235927 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77885183..77885373 26863196 MeRIP-seq:(Medium) rs1259700512 Functional Loss SNV dbSNP153 33..33 33 - - - 65978 RMVar_ID_65978 Human_SNP_ID_19587706 m1A Human chr1 + 77888651 77888651 77888651 GCGGCAGCCAGAGGACTCCCAGCGGCTGGAGCAGAAGTGTTAGCGGCCAGAGCTCCCAGACCCCT GCGGCAGCCAGAGGACTCCCAGCGGCTGGAGCGGAAGTGTTAGCGGCCAGAGCTCCCAGACCCCT A G NEXN Ensembl:ENSG00000162614 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:77888551..77888727;chr1:77888548..77917589 26863196 MeRIP-seq:(Medium) rs1030985530 Functional Loss SNV dbSNP153 33..33 33 - - - 65979 RMVar_ID_65979 Human_SNP_ID_19594203 m1A Human chr1 + 77918194 77918194 77918194 AAGACAAGAGGAACAAAGGAAGAGAACGGAGGAGGAACGAAAACGCAGAATTGAGCAGGATATGT AAGACAAGAGGAACAAAGGAAGAGAACGGAGGTGGAACGAAAACGCAGAATTGAGCAGGATATGT A T NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77918144..77918257 26863196 MeRIP-seq:(Medium) rs866906216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_88832,Human_Splice_Rec_88833,Human_Splice_Rec_88848,Human_Splice_Rec_88849,Human_Splice_Rec_88872,Human_Splice_Rec_88873,Human_Splice_Rec_88896,Human_Splice_Rec_88897,Human_Splice_Rec_88907 RMVar_hsa_circ_3933,RMVar_hsa_circ_68508,RMVar_hsa_circ_345068,RMVar_hsa_circ_50670 65980 RMVar_ID_65980 Human_SNP_ID_19597953 m1A Human chr1 + 77933434 77933434 77933434 CGAACAGAGGAGGAACGGAAGCATAAGCTAGAAATGGAGAAACAAGAATTTGAACAACTGAGACA CGAACAGAGGAGGAACGGAAGCATAAGCTAGACATGGAGAAACAAGAATTTGAACAACTGAGACA A C NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77933384..77935884 26863196 MeRIP-seq:(Medium) rs1446015584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2166458 Human_Splice_Rec_88859,Human_Splice_Rec_88883,Human_Splice_Rec_88905,Human_Splice_Rec_88917,Human_Splice_Rec_88929,Human_Splice_Rec_88933 RMVar_hsa_circ_68508,RMVar_hsa_circ_66970,RMVar_hsa_circ_134154,RMVar_hsa_circ_81737,RMVar_hsa_circ_356117 65981 RMVar_ID_65981 Human_SNP_ID_19600313 m1A Human chr1 + 77942142 77942142 77942142 GCTAAGGCAAGAGAAGAAGAAGAACAAAGAAGAATTGAAGAACAAAAGTTACTACGCATGCAGTT GCTAAGGCAAGAGAAGAAGAAGAACAAAGAAGGATTGAAGAACAAAAGTTACTACGCATGCAGTT A G NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:77942031..77942550 26863196 MeRIP-seq:(Medium) rs1359392123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_88863,Human_Splice_Rec_88887,Human_Splice_Rec_88921,Human_Splice_Rec_88937,Human_Splice_Rec_88939 RMVar_hsa_circ_134154,RMVar_hsa_circ_81737 65982 RMVar_ID_65982 Human_SNP_ID_19600317 m1A Human chr1 + 77942154 77942152 77942154 GAAGAAGAAGAACAAAGAAGAATTGAAGAACAAAAGTTACTACGCATGCAGTTTGAACAAAGGGA GAAGAAGAAGAACAAAGAAGAATTGAAGAAC__AAGTTACTACGCATGCAGTTTGAACAAAGGGA CAA C NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77942033..77942567 26863196 MeRIP-seq:(Medium) rs1394704286 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_88863,Human_Splice_Rec_88887,Human_Splice_Rec_88921,Human_Splice_Rec_88937,Human_Splice_Rec_88939 Clinvar_Rec_265 RMVar_hsa_circ_134154,RMVar_hsa_circ_81737 65983 RMVar_ID_65983 Human_SNP_ID_19600319 m1A Human chr1 + 77942154 77942154 77942154 GAAGAAGAAGAACAAAGAAGAATTGAAGAACAAAAGTTACTACGCATGCAGTTTGAACAAAGGGA GAAGAAGAAGAACAAAGAAGAATTGAAGAACAGAAGTTACTACGCATGCAGTTTGAACAAAGGGA A G NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77942033..77942567 26863196 MeRIP-seq:(Medium) rs778477679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_88863,Human_Splice_Rec_88887,Human_Splice_Rec_88921,Human_Splice_Rec_88937,Human_Splice_Rec_88939 Clinvar_Rec_266 RMVar_hsa_circ_134154,RMVar_hsa_circ_81737 65984 RMVar_ID_65984 Human_SNP_ID_19600464 m1A Human chr1 - 77942514 77942514 77942514 GGAGCTCCTGATCTGGTTTGCTCTTCATCTTCAGCAGTGGAGCCATTCATGATGCTACCTTCTTC GGAGCTCCTGATCTGGTTTGCTCTTCATCTTCGGCAGTGGAGCCATTCATGATGCTACCTTCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77942445..77942583 26863196 MeRIP-seq:(Medium) rs781511028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1435358 65985 RMVar_ID_65985 Human_SNP_ID_19601985 m1A Human chr1 - 77948724 77948724 77948724 GACAATACAGTATTTGCTTCATTGTGTGGGGGAAAAAAACCTTTGTTAAATATATGGATGCAGAC GACAATACAGTATTTGCTTCATTGTGTGGGGGGAAAAAACCTTTGTTAAATATATGGATGCAGAC T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:77948581..77948830 32194978 MeRIP-seq:(Medium) rs1313556954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1435414,Human_RBP_ID_1754458,Human_RBP_ID_3322480,Human_RBP_ID_5866792,Human_RBP_ID_8319533,Human_RBP_ID_11113679,Human_RBP_ID_17588607,Human_RBP_ID_18581296,Human_RBP_ID_22786192,Human_RBP_ID_23414197,Human_RBP_ID_24728412 Human_Splice_Rec_89052 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_82921,RMVar_hsa_circ_125144,RMVar_hsa_circ_134156,RMVar_hsa_circ_134157,RMVar_hsa_circ_23823,RMVar_hsa_circ_134158,RMVar_hsa_circ_103531,RMVar_hsa_circ_26413,RMVar_hsa_circ_119407,RMVar_hsa_circ_134159 65986 RMVar_ID_65986 Human_SNP_ID_19602048 m1A Human chr1 - 77948987 77948985 77948988 GGTGTATTGTTTGGGTTTTTTTGTTTTTTATAATGCTTTCCAGCATCTGAGTGGTGAATATTTCT GGTGTATTGTTTGGGTTTTTTTGTTTTTTAT___GCTTTCCAGCATCTGAGTGGTGAATATTTCT CATT C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:77948984..77949084 32194978 MeRIP-seq:(Medium) rs1296772115 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_363017,Human_RBP_ID_1754463,Human_RBP_ID_2166702,Human_RBP_ID_3322485,Human_RBP_ID_5866817,Human_RBP_ID_8319536,Human_RBP_ID_8975331,Human_RBP_ID_11113692,Human_RBP_ID_17588610,Human_RBP_ID_24398009,Human_RBP_ID_24454342,Human_RBP_ID_24728440 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_82921,RMVar_hsa_circ_125144,RMVar_hsa_circ_134156,RMVar_hsa_circ_134157,RMVar_hsa_circ_23823,RMVar_hsa_circ_134158,RMVar_hsa_circ_103531,RMVar_hsa_circ_26413,RMVar_hsa_circ_119407,RMVar_hsa_circ_134159 65987 RMVar_ID_65987 Human_SNP_ID_19602134 m1A Human chr1 - 77949280 77949280 77949280 TTTTTTTCAAAGGTCAGGCAGTTCCTGCTCCGACTGGGGCTCCTCCAGGTGGTCAGCCAGATTAT TTTTTTTCAAAGGTCAGGCAGTTCCTGCTCCGGCTGGGGCTCCTCCAGGTGGTCAGCCAGATTAT T C FUBP1 Ensembl:ENSG00000162613 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:77949232..77955336 32194978 MeRIP-seq:(Medium) rs587778376 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_222725,Human_RBP_ID_363020,Human_RBP_ID_743884,Human_RBP_ID_803180,Human_RBP_ID_859231,Human_RBP_ID_5866829,Human_RBP_ID_11113707,Human_RBP_ID_17758293,Human_RBP_ID_24454344,Human_RBP_ID_24556202,Human_RBP_ID_24745631 Human_Splice_Rec_88964,Human_Splice_Rec_88974,Human_Splice_Rec_89012,Human_Splice_Rec_89050,Human_Splice_Rec_89086,Human_Splice_Rec_89090 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_82921,RMVar_hsa_circ_125144,RMVar_hsa_circ_134156,RMVar_hsa_circ_134157,RMVar_hsa_circ_23823,RMVar_hsa_circ_40163,RMVar_hsa_circ_134158,RMVar_hsa_circ_103531,RMVar_hsa_circ_26413,RMVar_hsa_circ_119407,RMVar_hsa_circ_134159,RMVar_hsa_circ_312576,RMVar_hsa_circ_353103,RMVar_hsa_circ_366229,RMVar_hsa_circ_373357,RMVar_hsa_circ_366532,RMVar_hsa_circ_363901,RMVar_hsa_circ_318826,RMVar_hsa_circ_110758,RMVar_hsa_circ_297447,RMVar_hsa_circ_52533,RMVar_hsa_circ_134161,RMVar_hsa_circ_134163,RMVar_hsa_circ_21504,RMVar_hsa_circ_134164,RMVar_hsa_circ_134162 65988 RMVar_ID_65988 Human_SNP_ID_19604064 m1A Human chr1 - 77956621 77956621 77956621 GCTCACTATTATCAACAGCAAGCACAGCCACCACCAGCAGCCCCTGCAGGTGCACCAACTACAAC GCTCACTATTATCAACAGCAAGCACAGCCACCTCCAGCAGCCCCTGCAGGTGCACCAACTACAAC T A FUBP1 Ensembl:ENSG00000162613 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:77956539..77956641 26863196 MeRIP-seq:(Medium) rs746140021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22572,Human_RBP_ID_222728,Human_RBP_ID_803182,Human_RBP_ID_859234,Human_RBP_ID_3936266,Human_RBP_ID_5331751,Human_RBP_ID_9359015,Human_RBP_ID_17338245,Human_RBP_ID_17455070,Human_RBP_ID_22786236,Human_RBP_ID_26309778,Human_RBP_ID_26800660,Human_RBP_ID_26869763,Human_RBP_ID_27800481 Human_Splice_Rec_89008,Human_Splice_Rec_89009,Human_Splice_Rec_89046,Human_Splice_Rec_89047,Human_Splice_Rec_89082,Human_Splice_Rec_89083,Human_Splice_Rec_89094,Human_Splice_Rec_89095 Human_miRNA_ID_2050265 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_23823,RMVar_hsa_circ_92,RMVar_hsa_circ_40163,RMVar_hsa_circ_119407,RMVar_hsa_circ_134159,RMVar_hsa_circ_312576,RMVar_hsa_circ_353103,RMVar_hsa_circ_366229,RMVar_hsa_circ_366532,RMVar_hsa_circ_363901,RMVar_hsa_circ_318826,RMVar_hsa_circ_110758,RMVar_hsa_circ_297447,RMVar_hsa_circ_52533,RMVar_hsa_circ_134161,RMVar_hsa_circ_134163,RMVar_hsa_circ_21504,RMVar_hsa_circ_134162,RMVar_hsa_circ_24882,RMVar_hsa_circ_270876,RMVar_hsa_circ_310935,RMVar_hsa_circ_347526,RMVar_hsa_circ_79899,RMVar_hsa_circ_12000,RMVar_hsa_circ_134167,RMVar_hsa_circ_103833,RMVar_hsa_circ_134165,RMVar_hsa_circ_134166,RMVar_hsa_circ_268882,RMVar_hsa_circ_336091,RMVar_hsa_circ_108289,RMVar_hsa_circ_134169,RMVar_hsa_circ_12675,RMVar_hsa_circ_134168 65989 RMVar_ID_65989 Human_SNP_ID_19606278 m1A Human chr1 - 77964709 77964709 77964709 AAGGAAATGGTGTTAGAGTTAATTCGTGATCAAGGCGGTTTCAGAGAAGTTCGGAATGAGTATGG AAGGAAATGGTGTTAGAGTTAATTCGTGATCAGGGCGGTTTCAGAGAAGTTCGGAATGAGTATGG T C FUBP1 Ensembl:ENSG00000162613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:77964626..77964768;chr1:77964619..77964778 26863196 MeRIP-seq:(Medium) rs1189666711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22583,Human_RBP_ID_1435479,Human_RBP_ID_1754529,Human_RBP_ID_2184225,Human_RBP_ID_3322526,Human_RBP_ID_5538067,Human_RBP_ID_11114622,Human_RBP_ID_18430839,Human_RBP_ID_18968548,Human_RBP_ID_22559546,Human_RBP_ID_23414313,Human_RBP_ID_27798233 Human_Splice_Rec_88996,Human_Splice_Rec_88997,Human_Splice_Rec_89034,Human_Splice_Rec_89035,Human_Splice_Rec_89070,Human_Splice_Rec_89071 Human_miRNA_ID_3115548 RMVar_hsa_circ_81,RMVar_hsa_circ_92,RMVar_hsa_circ_40163,RMVar_hsa_circ_366229,RMVar_hsa_circ_363901,RMVar_hsa_circ_318826,RMVar_hsa_circ_21504,RMVar_hsa_circ_270876,RMVar_hsa_circ_347526,RMVar_hsa_circ_108289,RMVar_hsa_circ_134169,RMVar_hsa_circ_12675,RMVar_hsa_circ_3791,RMVar_hsa_circ_328050 65990 RMVar_ID_65990 Human_SNP_ID_19606281 m1A Human chr1 + 77964718 77964718 77964718 TTCCGAACTTCTCTGAAACCGCCTTGATCACGAATTAACTCTAACACCATTTCCTTGGCTTGCTA TTCCGAACTTCTCTGAAACCGCCTTGATCACGCATTAACTCTAACACCATTTCCTTGGCTTGCTA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:77964676..77964842 26863196 MeRIP-seq:(Medium) rs768059426 Functional Loss SNV dbSNP153 33..33 33 - - - 65991 RMVar_ID_65991 Human_SNP_ID_19606447 m1A Human chr1 - 77965189 77965189 77965189 CGGTTACTGGACCAGATTGTTGAAAAAGGAAGACCAGCTCCTGGCTTCCATCATGGCGATGGACC CGGTTACTGGACCAGATTGTTGAAAAAGGAAGCCCAGCTCCTGGCTTCCATCATGGCGATGGACC T G FUBP1 Ensembl:ENSG00000162613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77965042..77965250 26863196 MeRIP-seq:(Medium) rs1379301742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_363032,Human_RBP_ID_859246,Human_RBP_ID_1435482,Human_RBP_ID_1754535,Human_RBP_ID_5538070,Human_RBP_ID_9356513,Human_RBP_ID_11114641,Human_RBP_ID_22633892,Human_RBP_ID_22868551,Human_RBP_ID_23414315,Human_RBP_ID_26311466,Human_RBP_ID_27400996 Human_Splice_Rec_88992,Human_Splice_Rec_89030,Human_Splice_Rec_89066,Human_Splice_Rec_89110 Human_miRNA_ID_2290845,Human_miRNA_ID_2356192,Human_miRNA_ID_2991553,Human_miRNA_ID_3002987,Human_miRNA_ID_3058636 RMVar_hsa_circ_81,RMVar_hsa_circ_92,RMVar_hsa_circ_40163,RMVar_hsa_circ_366229,RMVar_hsa_circ_363901,RMVar_hsa_circ_318826,RMVar_hsa_circ_21504,RMVar_hsa_circ_270876,RMVar_hsa_circ_347526,RMVar_hsa_circ_12675,RMVar_hsa_circ_3791,RMVar_hsa_circ_328050,RMVar_hsa_circ_108005,RMVar_hsa_circ_74878,RMVar_hsa_circ_134174 65992 RMVar_ID_65992 Human_SNP_ID_19607798 m1A Human chr1 - 77970017 77970017 77970017 AGTTTATGATGGTATTTTTCTTTTTTTTTTTTAGATTGCAGCAAAAATTGGAGGTGATGCAGGGA AGTTTATGATGGTATTTTTCTTTTTTTTTTTTTGATTGCAGCAAAAATTGGAGGTGATGCAGGGA T A FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:77969997..77970080;chr1:77970001..77970025 26863196 MeRIP-seq:(Medium) rs1186391731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5867236,Human_RBP_ID_24556506 Human_Splice_Rec_88981,Human_Splice_Rec_89019,Human_Splice_Rec_89055,Human_Splice_Rec_89099 RMVar_hsa_circ_134177 65993 RMVar_ID_65993 Human_SNP_ID_19610489 m1A Human chr1 + 77978972 77978972 77978972 CCGCCGCCACCACCGCCACCAGCTGAGCCAGAAGAGGGGGGAGGCACTGTTGAATAGTCTGCCAT CCGCCGCCACCACCGCCACCAGCTGAGCCAGAGGAGGGGGGAGGCACTGTTGAATAGTCTGCCAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:77966738..77979011 32194978 MeRIP-seq:(Medium) rs1025863548 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 65994 RMVar_ID_65994 Human_SNP_ID_21118609 m1A Human chr1 - 84078126 84078114 84078126 AGGGCTCCAGCGAACTCCTTAGCACCGGCAGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGACGGC AGGGCTCCAGCGAACTCCTTAGCACCGGCAGC____________GGCGGCGGCGGCGGCGACGGC CGCCGCCGCTGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:84078076..84078451 26863196 MeRIP-seq:(Medium) rs1185824386 Functional Loss DEL dbSNP153 33..44 33 - - - 65995 RMVar_ID_65995 Human_SNP_ID_21118728 m1A Human chr1 - 84078402 84078402 84078402 GAGGGCGCTCGGTGCCCCGCGCCGGCCCGCCCAGCGGATACCCAGACCCGGCCTTCAACTCACCG GAGGGCGCTCGGTGCCCCGCGCCGGCCCGCCCCGCGGATACCCAGACCCGGCCTTCAACTCACCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:84078399..84078518 26863196 MeRIP-seq:(Medium) rs755986186 Functional Loss SNV dbSNP153 33..33 33 - - - 65996 RMVar_ID_65996 Human_SNP_ID_21118738 m1A Human chr1 + 84078422 84078422 84078422 CTGGGTATCCGCTGGGCGGGCCGGCGCGGGGCACCGAGCGCCCTCCGGGTCGCAGCTTCTGAGGC CTGGGTATCCGCTGGGCGGGCCGGCGCGGGGCGCCGAGCGCCCTCCGGGTCGCAGCTTCTGAGGC A G PRKACB Ensembl:ENSG00000142875 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:84078408..84078510 26863196 MeRIP-seq:(Medium) rs978598972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744974,Human_RBP_ID_26773107 65997 RMVar_ID_65997 Human_SNP_ID_21168680 m1A Human chr1 - 84292513 84292513 84292513 GATGCCAGTGTGGTTGGATATGGGCAGGGGTCAAGTAGAAGGAGGACAGGAAAACCCCGGGGCTG GATGCCAGTGTGGTTGGATATGGGCAGGGGTCGAGTAGAAGGAGGACAGGAAAACCCCGGGGCTG T C lnc-GNG5-9,lnc-GNG5-9:2,lnc-GNG5-9:3,lnc-GNG5-9:4,lnc-GNG5-9:5,lnc-GNG5-9:6,lnc-GNG5-9:7,lnc-GNG5-9:8,lnc-GNG5-9:9 RNACentral:URS0000D581CB,RNACentral:URS0000D59B40,RNACentral:URS0000D5B0C7,RNACentral:URS0000D56E19,RNACentral:URS0000D59C23,RNACentral:URS0000D5B331,RNACentral:URS0000D5CDF3,RNACentral:URS0000D5CC74,RNACentral:URS0000D5B3DA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,exon,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:84292393..84292573 26863196 MeRIP-seq:(Medium) rs528486114 Functional Loss SNV dbSNP153 33..33 33 - - - 65998 RMVar_ID_65998 Human_SNP_ID_21211006 m1A Human chr1 + 84479324 84479324 84479324 CCGGGGATAAGAGCAGCAGCAGCGGGAAGAAAAGTCTAAAACGGAAAGCCGCTGCCGAAGAACTT CCGGGGATAAGAGCAGCAGCAGCGGGAAGAAACGTCTAAAACGGAAAGCCGCTGCCGAAGAACTT A C RPF1 Ensembl:ENSG00000117133 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:84479251..84479525;chr1:84479251..84479500 26863196 MeRIP-seq:(Medium) rs1558536434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074139 65999 RMVar_ID_65999 Human_SNP_ID_21211007 m1A Human chr1 - 84479326 84479326 84479326 TGAAGTTCTTCGGCAGCGGCTTTCCGTTTTAGACTTTTCTTCCCGCTGCTGCTGCTCTTATCCCC TGAAGTTCTTCGGCAGCGGCTTTCCGTTTTAGCCTTTTCTTCCCGCTGCTGCTGCTCTTATCCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:84479276..84479429 26863196 MeRIP-seq:(Medium) rs1433633378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5869740 66000 RMVar_ID_66000 Human_SNP_ID_21211048 m1A Human chr1 + 84479404 84479404 84479404 GCTGGGGATGGGGCGACGGAAAACGGGGTCCAACCCCCGAAAGCGGCTGCCTTTCCGCCAGGCTT GCTGGGGATGGGGCGACGGAAAACGGGGTCCAGCCCCCGAAAGCGGCTGCCTTTCCGCCAGGCTT A G RPF1 Ensembl:ENSG00000117133 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:84479357..84479456 32194978 MeRIP-seq:(Medium) rs148206998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9359030,Human_RBP_ID_26311468 66001 RMVar_ID_66001 Human_SNP_ID_21211049 m1A Human chr1 + 84479404 84479404 84479404 GCTGGGGATGGGGCGACGGAAAACGGGGTCCAACCCCCGAAAGCGGCTGCCTTTCCGCCAGGCTT GCTGGGGATGGGGCGACGGAAAACGGGGTCCATCCCCCGAAAGCGGCTGCCTTTCCGCCAGGCTT A T RPF1 Ensembl:ENSG00000117133 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:84479357..84479456 32194978 MeRIP-seq:(Medium) rs148206998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9359030,Human_RBP_ID_26311468 66002 RMVar_ID_66002 Human_SNP_ID_21213941 m1A Human chr1 + 84490857 84490857 84490857 TGACTGGTACAAAGTCTGCCCTGGGAGGAAAGACTTCCCATAGAAAGAGATGCTGAAGCTGGATC TGACTGGTACAAAGTCTGCCCTGGGAGGAAAGTCTTCCCATAGAAAGAGATGCTGAAGCTGGATC A T RPF1 Ensembl:ENSG00000117133 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:84490855..84490987 26863196 MeRIP-seq:(Medium) rs572589715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23415646 RMVar_hsa_circ_42830 66003 RMVar_ID_66003 Human_SNP_ID_21217863 m1A Human chr1 - 84506057 84506057 84506057 GTCTGGCTCCTCCAGCGTCGCCGCTATGAAGAAAGTGGTTCAACAGCTCCGGCTGGAGGCCGGAC GTCTGGCTCCTCCAGCGTCGCCGCTATGAAGACAGTGGTTCAACAGCTCCGGCTGGAGGCCGGAC T G GNG5,AL359762.3 Ensembl:ENSG00000174021,Ensembl:ENSG00000285851 Protein coding,lincRNA CDS,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:84506001..84506175 26863196 MeRIP-seq:(Medium) rs1421870648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_363478,Human_RBP_ID_859632,Human_RBP_ID_4072885,Human_RBP_ID_5311761,Human_RBP_ID_8319971,Human_RBP_ID_8975982,Human_RBP_ID_9270210,Human_RBP_ID_9319008,Human_RBP_ID_9356520,Human_RBP_ID_22429457,Human_RBP_ID_23415675,Human_RBP_ID_26311473,Human_RBP_ID_26798550,Human_RBP_ID_26870413 Human_Splice_Rec_91799,Human_Splice_Rec_91803 Human_miRNA_ID_2975975 RMVar_hsa_circ_86787,RMVar_hsa_circ_134271 66004 RMVar_ID_66004 Human_SNP_ID_21217912 m1A Human chr1 - 84506127 84506127 84506127 GTCTGGCCCCGCCGACCCACGGCCCACGACCCACCGACCCACGAATCGGCCCGGCCGTCGCGTGC GTCTGGCCCCGCCGACCCACGGCCCACGACCCCCCGACCCACGAATCGGCCCGGCCGTCGCGTGC T G GNG5,AL359762.3 Ensembl:ENSG00000174021,Ensembl:ENSG00000285851 Protein coding,lincRNA 5'UTR,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:84506069..84506179 26863410 MeRIP-seq:(Medium) rs1394964077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222919,Human_RBP_ID_363482,Human_RBP_ID_801985,Human_RBP_ID_4072886,Human_RBP_ID_17338255,Human_RBP_ID_22559554,Human_RBP_ID_26798552,Human_RBP_ID_26870413 RMVar_hsa_circ_86787,RMVar_hsa_circ_134271 66005 RMVar_ID_66005 Human_SNP_ID_21217929 m1A Human chr1 - 84506141 84506141 84506141 CGCGCCGCTGAGTTGTCTGGCCCCGCCGACCCACGGCCCACGACCCACCGACCCACGAATCGGCC CGCGCCGCTGAGTTGTCTGGCCCCGCCGACCCTCGGCCCACGACCCACCGACCCACGAATCGGCC T A GNG5,AL359762.3 Ensembl:ENSG00000174021,Ensembl:ENSG00000285851 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:84505980..84506885;chr1:84506001..84506200;chr1:84505956..84506275;chr1:84505936..84506736;chr1:84505947..84506253 26863196 MeRIP-seq:(Medium) rs1394648960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222919,Human_RBP_ID_363484,Human_RBP_ID_801985,Human_RBP_ID_4072886,Human_RBP_ID_5486935,Human_RBP_ID_9319010,Human_RBP_ID_17338256,Human_RBP_ID_22429459,Human_RBP_ID_22559554,Human_RBP_ID_26798553 RMVar_hsa_circ_86787,RMVar_hsa_circ_134271 66006 RMVar_ID_66006 Human_SNP_ID_21217935 m1A Human chr1 - 84506145 84506145 84506145 GCCGCGCGCCGCTGAGTTGTCTGGCCCCGCCGACCCACGGCCCACGACCCACCGACCCACGAATC GCCGCGCGCCGCTGAGTTGTCTGGCCCCGCCGCCCCACGGCCCACGACCCACCGACCCACGAATC T G GNG5,AL359762.3 Ensembl:ENSG00000174021,Ensembl:ENSG00000285851 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:84506101..84506150 26863196 MeRIP-seq:(Medium) rs1315047609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222919,Human_RBP_ID_363484,Human_RBP_ID_801985,Human_RBP_ID_4072886,Human_RBP_ID_5486935,Human_RBP_ID_9319010,Human_RBP_ID_17338256,Human_RBP_ID_22427327,Human_RBP_ID_22559554,Human_RBP_ID_26798553 RMVar_hsa_circ_86787,RMVar_hsa_circ_134271 66007 RMVar_ID_66007 Human_SNP_ID_21228432 m1A Human chr1 - 84553935 84553935 84553935 TCAACTAGTTCTCTTTCTAAAAGATCAATTTTATACAAATAAGTTTTCTAAATGTAATAAAGTCT TCAACTAGTTCTCTTTCTAAAAGATCAATTTTTTACAAATAAGTTTTCTAAATGTAATAAAGTCT T A CTBS,AL359762.3 Ensembl:ENSG00000117151,Ensembl:ENSG00000285851 Protein coding,lincRNA 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:84553921..84554008 32194978 MeRIP-seq:(Medium) rs1447839740 Functional Loss SNV dbSNP153 33..33 33 - - - 66008 RMVar_ID_66008 Human_SNP_ID_21233173 m1A Human chr1 + 84574336 84574336 84574336 CGGCCGCGAGCCGCAGCGCCAGCAGCGCCAGCAGCGCCAGCAGCGCTAGACCCGGGACGCCGCTC CGGCCGCGAGCCGCAGCGCCAGCAGCGCCAGCGGCGCCAGCAGCGCTAGACCCGGGACGCCGCTC A G AL359762.1 Ensembl:ENSG00000284882 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:84574288..84574359;chr1:84574290..84574360 26863196 MeRIP-seq:(Medium) rs751607399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_91901 66009 RMVar_ID_66009 Human_SNP_ID_21259980 m1A Human chr1 + 84690416 84690416 84690416 GGGAGCGGCGGGGAGTCACCGCTCGGCGTCCTAGCCCGGCTCCCGCAGCCCGAGGGCCAGCAGCG GGGAGCGGCGGGGAGTCACCGCTCGGCGTCCTCGCCCGGCTCCCGCAGCCCGAGGGCCAGCAGCG A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:84690372..84690465 26863410 MeRIP-seq:(Medium) rs1435582505 Functional Loss SNV dbSNP153 33..33 33 - - - 66010 RMVar_ID_66010 Human_SNP_ID_21259996 m1A Human chr1 + 84690455 84690455 84690455 CTCCCGCAGCCCGAGGGCCAGCAGCGCCTCGCAGCGCCTCCCGCCCGCGGCCCCTCCTCCGCTGC CTCCCGCAGCCCGAGGGCCAGCAGCGCCTCGCCGCGCCTCCCGCCCGCGGCCCCTCCTCCGCTGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:84671287..84690542;chr1:84671287..84690533 26863196 MeRIP-seq:(Medium) rs1486012844 Functional Loss SNV dbSNP153 33..33 33 - - - 66011 RMVar_ID_66011 Human_SNP_ID_21332962 m1A Human chr1 - 84996982 84996982 84996982 AGAAAGGGTAAGAGAAGGGAACCCCGCTTTGCAGGGCTCCAACTTCGGCGGACGCGTTACGGCGA AGAAAGGGTAAGAGAAGGGAACCCCGCTTTGCCGGGCTCCAACTTCGGCGGACGCGTTACGGCGA T G MCOLN2 Ensembl:ENSG00000153898 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11161505 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7919,GWAS_ID_7920,GWAS_ID_7921,GWAS_ID_7922,GWAS_ID_7923,GWAS_ID_7924,GWAS_ID_7925,GWAS_ID_7926,GWAS_ID_7927 66012 RMVar_ID_66012 Human_SNP_ID_21344570 m1A Human chr1 + 85048447 85048447 85048447 GGCCGCAGCTCCGGTGTCCGCGGCGAGGGCGCAGGGCGAGTCAGCGAGCGACTCCAGCAGCCTCG GGCCGCAGCTCCGGTGTCCGCGGCGAGGGCGCCGGGCGAGTCAGCGAGCGACTCCAGCAGCCTCG A C WDR63 Ensembl:ENSG00000162643 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:85048224..85048680;chr1:85048239..85048589 26863196 MeRIP-seq:(Medium) rs1408683918 Functional Loss SNV dbSNP153 33..33 33 - - - 66013 RMVar_ID_66013 Human_SNP_ID_21379545 m1A Human chr1 - 85200698 85200698 85200698 CCTCCGGGTGGGTGCCAAGCCGCCTCCCTTCCAGCGGTGGCCGAGCGACAGCTGGATCAGGTGCG CCTCCGGGTGGGTGCCAAGCCGCCTCCCTTCCGGCGGTGGCCGAGCGACAGCTGGATCAGGTGCG T C SYDE2 Ensembl:ENSG00000097096 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:85200647..85200962 26863196 MeRIP-seq:(Medium) rs1255063570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8755045,Human_RBP_ID_9270216 66014 RMVar_ID_66014 Human_SNP_ID_21379780 m1A Human chr1 - 85201205 85201203 85201206 CTCCGAGGACAGCGGAGAGGAGGAGGAAGACGACAAGGACGAAGACGACTACGACGCCGACTACT CTCCGAGGACAGCGGAGAGGAGGAGGAAGAC___AAGGACGAAGACGACTACGACGCCGACTACT TGTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:85201155..85201698 26863196 MeRIP-seq:(Medium) rs1302307403 Functional Loss DEL dbSNP153 32..34 33 - - - 66015 RMVar_ID_66015 Human_SNP_ID_21379782 m1A Human chr1 - 85201205 85201205 85201205 CTCCGAGGACAGCGGAGAGGAGGAGGAAGACGACAAGGACGAAGACGACTACGACGCCGACTACT CTCCGAGGACAGCGGAGAGGAGGAGGAAGACGGCAAGGACGAAGACGACTACGACGCCGACTACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:85201155..85201698 26863196 MeRIP-seq:(Medium) rs1454419108 Functional Loss SNV dbSNP153 33..33 33 - - - 66016 RMVar_ID_66016 Human_SNP_ID_21380071 m1A Human chr1 - 85201864 85201864 85201864 ACCGGCCCGCGCCCTCCGCCTCCACCTGCACCACTCGCCCACCCCGAGAACCCACCTCTGCCGCC ACCGGCCCGCGCCCTCCGCCTCCACCTGCACCTCTCGCCCACCCCGAGAACCCACCTCTGCCGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:85201815..85202027 26863196 MeRIP-seq:(Medium) rs1431047464 Functional Loss SNV dbSNP153 33..33 33 - - - 66017 RMVar_ID_66017 Human_SNP_ID_21380082 m1A Human chr1 - 85201896 85201896 85201896 CGGTCAGCTTCAGCCGACCTACTACTCAACCTACCGGCCCGCGCCCTCCGCCTCCACCTGCACCA CGGTCAGCTTCAGCCGACCTACTACTCAACCTGCCGGCCCGCGCCCTCCGCCTCCACCTGCACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:85201773..85202036 26863196 MeRIP-seq:(Medium) rs1366478656 Functional Loss SNV dbSNP153 33..33 33 - - - 66018 RMVar_ID_66018 Human_SNP_ID_21393259 m1A Human chr1 + 85259610 85259610 85259610 CTGCTGCTCCCGTATGCCGCAAAATAGCTCAGAGGGTCCTTCTCCTCCGCTGCCATGACGGCTGC CTGCTGCTCCCGTATGCCGCAAAATAGCTCAGCGGGTCCTTCTCCTCCGCTGCCATGACGGCTGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:85259404..85259675;chr1:85259424..85259675 26863196 MeRIP-seq:(Medium) rs749601140 Functional Loss SNV dbSNP153 33..33 33 - - - 66019 RMVar_ID_66019 Human_SNP_ID_21393260 m1A Human chr1 + 85259610 85259610 85259610 CTGCTGCTCCCGTATGCCGCAAAATAGCTCAGAGGGTCCTTCTCCTCCGCTGCCATGACGGCTGC CTGCTGCTCCCGTATGCCGCAAAATAGCTCAGGGGGTCCTTCTCCTCCGCTGCCATGACGGCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:85259404..85259675;chr1:85259424..85259675 26863196 MeRIP-seq:(Medium) rs749601140 Functional Loss SNV dbSNP153 33..33 33 - - - 66020 RMVar_ID_66020 Human_SNP_ID_21439394 m1A Human chr1 - 85465114 85465114 85465114 GCCAAGAGGAGCCGACGGGCGCTCGCAGGCTCAGCGCGCGCTGCCCGCGGCAGGACCCGGCCGCC GCCAAGAGGAGCCGACGGGCGCTCGCAGGCTCGGCGCGCGCTGCCCGCGGCAGGACCCGGCCGCC T C DDAH1 Ensembl:ENSG00000153904 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control;HEPG2 cell line,mRNA Glucose starvation 4h chr1:85465026..85465150;chr1:85465038..85465129;chr1:85465046..85465130;chr1:85464711..85465150 26863410,26863196 MeRIP-seq:(Medium) rs1020782062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4067515,Human_RBP_ID_9359032,Human_RBP_ID_23416470 RMVar_hsa_circ_94765,RMVar_hsa_circ_111414,RMVar_hsa_circ_134296,RMVar_hsa_circ_93310,RMVar_hsa_circ_134294,RMVar_hsa_circ_134295,RMVar_hsa_circ_23654,RMVar_hsa_circ_113845,RMVar_hsa_circ_134306 66021 RMVar_ID_66021 Human_SNP_ID_21439395 m1A Human chr1 - 85465114 85465114 85465114 GCCAAGAGGAGCCGACGGGCGCTCGCAGGCTCAGCGCGCGCTGCCCGCGGCAGGACCCGGCCGCC GCCAAGAGGAGCCGACGGGCGCTCGCAGGCTCCGCGCGCGCTGCCCGCGGCAGGACCCGGCCGCC T G DDAH1 Ensembl:ENSG00000153904 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control;HEPG2 cell line,mRNA Glucose starvation 4h chr1:85465026..85465150;chr1:85465038..85465129;chr1:85465046..85465130;chr1:85464711..85465150 26863410,26863196 MeRIP-seq:(Medium) rs1020782062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4067515,Human_RBP_ID_9359032,Human_RBP_ID_23416470 RMVar_hsa_circ_94765,RMVar_hsa_circ_111414,RMVar_hsa_circ_134296,RMVar_hsa_circ_93310,RMVar_hsa_circ_134294,RMVar_hsa_circ_134295,RMVar_hsa_circ_23654,RMVar_hsa_circ_113845,RMVar_hsa_circ_134306 66022 RMVar_ID_66022 Human_SNP_ID_21439455 m1A Human chr1 - 85465258 85465258 85465258 GCCTGGGCTGGCGCGAGACCCGCGAGCGCCGGAGTGGGCGCGCGGGATGCGCGCGGGCCGGCGCC GCCTGGGCTGGCGCGAGACCCGCGAGCGCCGGGGTGGGCGCGCGGGATGCGCGCGGGCCGGCGCC T C DDAH1 Ensembl:ENSG00000153904 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:85465207..85465403 26863196 MeRIP-seq:(Medium) rs1337203922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94765,RMVar_hsa_circ_93310,RMVar_hsa_circ_134294,RMVar_hsa_circ_134295,RMVar_hsa_circ_23654 66023 RMVar_ID_66023 Human_SNP_ID_21447471 m1A Human chr1 - 85500194 85500191 85500195 AAAAAAGAAAGGAAGGAAGGAAGAAAGGAAGGAAGAAAAGATGAAGGAAGGAAGGAAAAAAGAGA AAAAAAGAAAGGAAGGAAGGAAGAAAGGAAG____AAAAGATGAAGGAAGGAAGGAAAAAAGAGA TCTTC T DDAH1,AC092807.4 Ensembl:ENSG00000153904,Ensembl:ENSG00000282057 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:85500145..85500229 26863196 MeRIP-seq:(Medium) rs1318546009 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_93310,RMVar_hsa_circ_134294 66024 RMVar_ID_66024 Human_SNP_ID_21467814 m1A Human chr1 + 85580930 85580930 85580930 CCCCGCTGCGCACGGCCTGTCCGCTGCACACCAGCTTGTTGGCGTCTTCGTCGCCGCGCTCGCCC CCCCGCTGCGCACGGCCTGTCCGCTGCACACCGGCTTGTTGGCGTCTTCGTCGCCGCGCTCGCCC A G CCN1 Ensembl:ENSG00000142871 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:85580751..85581400 26863196 MeRIP-seq:(Medium) rs1282762983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4067567 66025 RMVar_ID_66025 Human_SNP_ID_21467827 m1A Human chr1 - 85580957 85580957 85580957 CTCATTGTGGCGCGCAGGAGTAGCCCGGGGCGAGCGCGGCGACGAAGACGCCAACAAGCTGGTGT CTCATTGTGGCGCGCAGGAGTAGCCCGGGGCGGGCGCGGCGACGAAGACGCCAACAAGCTGGTGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:85580776..85581050;chr1:85580776..85581207 32194978 MeRIP-seq:(Medium) rs1172964168 Functional Loss SNV dbSNP153 33..33 33 - - - 66026 RMVar_ID_66026 Human_SNP_ID_21468255 m1A Human chr1 + 85582144 85582144 85582144 CGGGCAGTGCTGCGAGGAGTGGGTCTGTGACGAGGATAGTATCAAGGACCCCATGGAGGACCAGG CGGGCAGTGCTGCGAGGAGTGGGTCTGTGACGGGGATAGTATCAAGGACCCCATGGAGGACCAGG A G CCN1 Ensembl:ENSG00000142871 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:85582093..85582181 26863196 MeRIP-seq:(Medium) rs756289707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24962,Human_RBP_ID_22375961,Human_RBP_ID_22751078 RMVar_hsa_circ_134307,RMVar_hsa_circ_334552 66027 RMVar_ID_66027 Human_SNP_ID_21468399 m1A Human chr1 + 85582535 85582535 85582535 AGACCTGTGGAACTGGTATCTCCACACGAGTTACCAATGACAACCCTGAGTGCCGCCTTGTGAAA AGACCTGTGGAACTGGTATCTCCACACGAGTTGCCAATGACAACCCTGAGTGCCGCCTTGTGAAA A G CCN1 Ensembl:ENSG00000142871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:85582484..85582568 26863196 MeRIP-seq:(Medium) rs200203130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_92599 RMVar_hsa_circ_134307,RMVar_hsa_circ_334552 66028 RMVar_ID_66028 Human_SNP_ID_21497899 m1A Human chr1 - 85707804 85707804 85707804 CAGAAGTGAAGGAAGAGAAGGATAACTTGGAGATAAAACAGGAGGAGAAGTTTGTTGGTCAATGC CAGAAGTGAAGGAAGAGAAGGATAACTTGGAGGTAAAACAGGAGGAGAAGTTTGTTGGTCAATGC T C ZNHIT6 Ensembl:ENSG00000117174 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:85707753..85708282 26863196 MeRIP-seq:(Medium) rs748648102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3323809,Human_RBP_ID_4099437,Human_RBP_ID_5872464,Human_RBP_ID_9342150,Human_RBP_ID_9566528,Human_RBP_ID_11127103,Human_RBP_ID_17759306,Human_RBP_ID_22870875,Human_RBP_ID_23416841,Human_RBP_ID_26311484 Human_miRNA_ID_1436569,Human_miRNA_ID_1538119,Human_miRNA_ID_1592552,Human_miRNA_ID_1757343 RMVar_hsa_circ_134311 66029 RMVar_ID_66029 Human_SNP_ID_21497909 m1A Human chr1 - 85707842 85707842 85707842 AAAGGAAGAGAAGGTAAAGGAAGAGGTAATGGACTGGTCAGAAGTGAAGGAAGAGAAGGATAACT AAAGGAAGAGAAGGTAAAGGAAGAGGTAATGGGCTGGTCAGAAGTGAAGGAAGAGAAGGATAACT T C ZNHIT6 Ensembl:ENSG00000117174 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:85707799..85708024 26863196 MeRIP-seq:(Medium) rs1223926952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2169156,Human_RBP_ID_4067666,Human_RBP_ID_5872465,Human_RBP_ID_11127105,Human_RBP_ID_22870875,Human_RBP_ID_23416841,Human_RBP_ID_24541491,Human_RBP_ID_26311484,Human_RBP_ID_27835253 Human_Splice_Rec_92624 RMVar_hsa_circ_134312,RMVar_hsa_circ_134311 66030 RMVar_ID_66030 Human_SNP_ID_21735802 m1A Human chr1 - 86704689 86704689 86704689 GGGAGGAGAACAAGCGCGCGGCGGCAGCGCCAAGGATGGGTCAGTCGGCTCGGAGAACGGCCGCT GGGAGGAGAACAAGCGCGCGGCGGCAGCGCCAGGGATGGGTCAGTCGGCTCGGAGAACGGCCGCT T C CLCA4-AS1,CLCA4-AS1:2,CLCA4-AS1:3 RNACentral:URS0000D592FA,RNACentral:URS0000D596A0,RNACentral:URS00009B04BE lincRNA,lincRNA,lincRNA exon,exon,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:86704638..86704852 26863196 MeRIP-seq:(Medium) rs1384032830 Functional Loss SNV dbSNP153 33..33 33 - - - 66031 RMVar_ID_66031 Human_SNP_ID_21735810 m1A Human chr1 - 86704713 86704713 86704713 ACGGGGAGGATGAAGGCGGGGCGAGGGAGGAGAACAAGCGCGCGGCGGCAGCGCCAAGGATGGGT ACGGGGAGGATGAAGGCGGGGCGAGGGAGGAGGACAAGCGCGCGGCGGCAGCGCCAAGGATGGGT T C CLCA4-AS1,CLCA4-AS1:2,CLCA4-AS1:3 RNACentral:URS0000D592FA,RNACentral:URS0000D596A0,RNACentral:URS00009B04BE lincRNA,lincRNA,lincRNA exon,exon,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:86704631..86704713 26863410 MeRIP-seq:(Medium) rs1362007282 Functional Loss SNV dbSNP153 33..33 33 - - - 66032 RMVar_ID_66032 Human_SNP_ID_21735857 m1A Human chr1 - 86704825 86704825 86704825 GAGGCGGAGGTGCCGCGGCCGGGCTGGGGCGCAGGGCTAGAGCGGCGAGGGCAGACGTGGTAGGT GAGGCGGAGGTGCCGCGGCCGGGCTGGGGCGCCGGGCTAGAGCGGCGAGGGCAGACGTGGTAGGT T G CLCA4-AS1,CLCA4-AS1:2,CLCA4-AS1:3 RNACentral:URS0000D592FA,RNACentral:URS0000D596A0,RNACentral:URS00009B04BE lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:86704615..86704899;chr1:86704610..86704969 26863196 MeRIP-seq:(Medium) rs918915937 Functional Loss SNV dbSNP153 33..33 33 - - - 66033 RMVar_ID_66033 Human_SNP_ID_21745677 m1A Human chr1 + 86746257 86746257 86746257 ATTTCTGGGATAAACTGTGGAGTGGAGAAGACAATGGAGGGCAAGGCAAAAACCCACAGACTTGT ATTTCTGGGATAAACTGTGGAGTGGAGAAGACCATGGAGGGCAAGGCAAAAACCCACAGACTTGT A C SH3GLB1 Ensembl:ENSG00000097033 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10489890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364206,Human_RBP_ID_26383735 GWAS_ID_7928,GWAS_ID_7929,GWAS_ID_7930,GWAS_ID_7931,GWAS_ID_7932,GWAS_ID_7933,GWAS_ID_7934,GWAS_ID_7935,GWAS_ID_7936,GWAS_ID_7937 RMVar_hsa_circ_134342,RMVar_hsa_circ_105797 66034 RMVar_ID_66034 Human_SNP_ID_21775078 m1A Human chr1 - 86863492 86863492 86863492 AACACAGACAGTGTAGAAGAATTCCTGAGTGAAAAGTTGGAACGCATATAAATCTTGCTTAAATT AACACAGACAGTGTAGAAGAATTCCTGAGTGAGAAGTTGGAACGCATATAAATCTTGCTTAAATT T C SELENOF Ensembl:ENSG00000183291 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:86863373..86863569 32194978 MeRIP-seq:(Medium) rs372762020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364282,Human_RBP_ID_980185,Human_RBP_ID_1436046,Human_RBP_ID_1755450,Human_RBP_ID_5156212,Human_RBP_ID_11129479,Human_RBP_ID_18582116,Human_RBP_ID_23417458,Human_RBP_ID_26391232 66035 RMVar_ID_66035 Human_SNP_ID_21785716 m1A Human chr1 - 86903376 86903376 86903376 GAGAGTTAGGCTTTTCTAGCAACTTGCTTTGCAGCTCTTGTGATCTTCTCGGACAGTTCAACCTG GAGAGTTAGGCTTTTCTAGCAACTTGCTTTGCGGCTCTTGTGATCTTCTCGGACAGTTCAACCTG T C SELENOF Ensembl:ENSG00000183291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:86903326..86903496 26863196 MeRIP-seq:(Medium) rs11555170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364322,Human_RBP_ID_1436092,Human_RBP_ID_1755508,Human_RBP_ID_2169764,Human_RBP_ID_4074158,Human_RBP_ID_5486963,Human_RBP_ID_5873747,Human_RBP_ID_8320564,Human_RBP_ID_9270219,Human_RBP_ID_11130909,Human_RBP_ID_17762702,Human_RBP_ID_18582149,Human_RBP_ID_22147751,Human_RBP_ID_22749243,Human_RBP_ID_23112554,Human_RBP_ID_24746795 Human_Splice_Rec_93478,Human_Splice_Rec_93479,Human_Splice_Rec_93486,Human_Splice_Rec_93487,Human_Splice_Rec_93492,Human_Splice_Rec_93493,Human_Splice_Rec_93500,Human_Splice_Rec_93501,Human_Splice_Rec_93506,Human_Splice_Rec_93507,Human_Splice_Rec_93515,Human_Splice_Rec_93522,Human_Splice_Rec_93523,Human_Splice_Rec_93531,Human_Splice_Rec_93538,Human_Splice_Rec_93539 Human_miRNA_ID_2437587,Human_miRNA_ID_2778801 RMVar_hsa_circ_134345,RMVar_hsa_circ_28952,RMVar_hsa_circ_113409 66036 RMVar_ID_66036 Human_SNP_ID_21785744 m1A Human chr1 + 86903445 86903445 86903445 TGCCTCCGATGAAAACTCTGCCCCAAAAGCAGACACCTGAAAATAAAAAATGGGAAATAAAACAC TGCCTCCGATGAAAACTCTGCCCCAAAAGCAGGCACCTGAAAATAAAAAATGGGAAATAAAACAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:86903351..86913837;chr1:86903326..86903487;chr1:86903351..86903501 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1351070023 Functional Loss SNV dbSNP153 33..33 33 - - - 66037 RMVar_ID_66037 Human_SNP_ID_21785745 m1A Human chr1 + 86903447 86903447 86903447 CCTCCGATGAAAACTCTGCCCCAAAAGCAGACACCTGAAAATAAAAAATGGGAAATAAAACACAA CCTCCGATGAAAACTCTGCCCCAAAAGCAGACGCCTGAAAATAAAAAATGGGAAATAAAACACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:86903351..86903500 26863196 MeRIP-seq:(Medium) rs760296017 Functional Loss SNV dbSNP153 33..33 33 - - - 66038 RMVar_ID_66038 Human_SNP_ID_21788307 m1A Human chr1 + 86914094 86914094 86914094 CCAAACGCCGGCACCAGACACCCACTCGGCCCAGCCGCCATCGCTACCATTTTCCGCAGGTTTCT CCAAACGCCGGCACCAGACACCCACTCGGCCCTGCCGCCATCGCTACCATTTTCCGCAGGTTTCT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:86914026..86914125 26863196 MeRIP-seq:(Medium) rs770337757 Functional Loss SNV dbSNP153 33..33 33 - - - 66039 RMVar_ID_66039 Human_SNP_ID_21826531 m1A Human chr1 + 87072905 87072905 87072905 GTGTTCATAACTTCCTTATAGTGTCCTTAAAAACTTAGTTCGTATCTGTTTTTCTTTCCAGAAAG GTGTTCATAACTTCCTTATAGTGTCCTTAAAATCTTAGTTCGTATCTGTTTTTCTTTCCAGAAAG A T HS2ST1,AC093155.3 Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:87072904..87072999 26863196 MeRIP-seq:(Medium) rs1384645510 Functional Loss SNV dbSNP153 33..33 33 - - - 66040 RMVar_ID_66040 Human_SNP_ID_21886729 m1A Human chr1 - 87328909 87328909 87328909 CGGCCCGCGCGGCGCGGCTTCAGGCGCGGCGCAGCGGCAGCAACTGCTGCAATCGCTGCTGCAAG CGGCCCGCGCGGCGCGGCTTCAGGCGCGGCGCTGCGGCAGCAACTGCTGCAATCGCTGCTGCAAG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:87328816..87328966 26863410 MeRIP-seq:(Medium) rs1013346510 Functional Loss SNV dbSNP153 33..33 33 - - - 66041 RMVar_ID_66041 Human_SNP_ID_21887696 m1A Human chr1 + 87331690 87331690 87331690 GGCGGAGGCGGGGGCTGGGAGGAGGTGCCGCGAGGGGTGGAGCGCGCAGCGGAGCCTGCTCTCGG GGCGGAGGCGGGGGCTGGGAGGAGGTGCCGCGGGGGGTGGAGCGCGCAGCGGAGCCTGCTCTCGG A G LMO4 Ensembl:ENSG00000143013 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:87331682..87331849 26863196 MeRIP-seq:(Medium) rs968411536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328509,Human_RBP_ID_5311769,Human_RBP_ID_8167109,Human_RBP_ID_9411932,Human_RBP_ID_22559591,Human_RBP_ID_26773108 66042 RMVar_ID_66042 Human_SNP_ID_21887704 m1A Human chr1 + 87331705 87331705 87331705 TGGGAGGAGGTGCCGCGAGGGGTGGAGCGCGCAGCGGAGCCTGCTCTCGGAGTTTTGACAGTACC TGGGAGGAGGTGCCGCGAGGGGTGGAGCGCGCCGCGGAGCCTGCTCTCGGAGTTTTGACAGTACC A C LMO4 Ensembl:ENSG00000143013 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:87331685..87331954 26863196 MeRIP-seq:(Medium) rs931874259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328509,Human_RBP_ID_5311769,Human_RBP_ID_8167109,Human_RBP_ID_9411932,Human_RBP_ID_22559591,Human_RBP_ID_26773108 66043 RMVar_ID_66043 Human_SNP_ID_21888761 m1A Human chr1 + 87335349 87335349 87335349 TCCGGGGAGGGCGAGGAAACGCGCCGGAAGCCAGGGTGGCGGTCGTCGGCTGGCCCTCGCTCCCT TCCGGGGAGGGCGAGGAAACGCGCCGGAAGCCTGGGTGGCGGTCGTCGGCTGGCCCTCGCTCCCT A T LMO4 Ensembl:ENSG00000143013 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:87335309..87335438 26863196 MeRIP-seq:(Medium) rs1329006061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224027,Human_RBP_ID_3330353,Human_RBP_ID_5233998,Human_RBP_ID_8167110,Human_RBP_ID_18455640,Human_RBP_ID_26774419 RMVar_hsa_circ_348955 66044 RMVar_ID_66044 Human_SNP_ID_22197718 m1A Human chr1 + 88684339 88684339 88684339 GGCTCCTGGCGTCGCCCAGAGGGAGCGACTAGACGAACAGTCCGGTGAGGGCGGCGAGAGGAAGC GGCTCCTGGCGTCGCCCAGAGGGAGCGACTAGGCGAACAGTCCGGTGAGGGCGGCGAGAGGAAGC A G PKN2 Ensembl:ENSG00000065243 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:88684288..88684462;chr1:88684290..88684484 26863196 MeRIP-seq:(Medium) rs1043706177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1436280,Human_RBP_ID_4068389,Human_RBP_ID_9356524,Human_RBP_ID_11136191,Human_RBP_ID_18414999,Human_RBP_ID_18582366 66045 RMVar_ID_66045 Human_SNP_ID_22197735 m1A Human chr1 + 88684410 88684410 88684410 CGAGTGCCCTAGCTCCCCGCCGCTCTCGATGAACCGGACGGAATAAGCCGCGCCTCCAGCAGGGG CGAGTGCCCTAGCTCCCCGCCGCTCTCGATGAGCCGGACGGAATAAGCCGCGCCTCCAGCAGGGG A G PKN2 Ensembl:ENSG00000065243 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:88684316..88684442 26863410 MeRIP-seq:(Medium) rs1018120996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1436281,Human_RBP_ID_4072907,Human_RBP_ID_5486980,Human_RBP_ID_8320885,Human_RBP_ID_11136193,Human_RBP_ID_18582367 66046 RMVar_ID_66046 Human_SNP_ID_22223105 m1A Human chr1 - 88789313 88789313 88789313 CCGTTTCACTCCTGTCATCATACTGTCATACCAGTAACTATAATCCTTCCACAATCTCAACTGTC CCGTTTCACTCCTGTCATCATACTGTCATACCGGTAACTATAATCCTTCCACAATCTCAACTGTC T C lnc-GTF2B-6 RNACentral:URS00009C35F6 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:88789230..88789332 26863196 MeRIP-seq:(Medium) rs1292965501 Functional Loss SNV dbSNP153 33..33 33 - - - 66047 RMVar_ID_66047 Human_SNP_ID_22238843 m1A Human chr1 + 88853287 88853287 88853287 GTCTGTAGGAAACAGATCTGGGGCTCGAGGATAGATCAGTCTATAGGACTGTCTGATTGTAACAT GTCTGTAGGAAACAGATCTGGGGCTCGAGGATGGATCAGTCTATAGGACTGTCTGATTGTAACAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:88853178..88857384 32194978 MeRIP-seq:(Medium) rs765545366 Functional Loss SNV dbSNP153 33..33 33 - - - 66048 RMVar_ID_66048 Human_SNP_ID_22242362 m1A Human chr1 + 88866889 88866889 88866889 GAAGCAGGACAGTAAGTTAGAAGGCAATTTTAATACATCACACATTGAGCAGGTGGCCCGAAACA GAAGCAGGACAGTAAGTTAGAAGGCAATTTTAGTACATCACACATTGAGCAGGTGGCCCGAAACA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:88866796..88866909 26863196 MeRIP-seq:(Medium) rs1238708092 Functional Loss SNV dbSNP153 33..33 33 - - - 66049 RMVar_ID_66049 Human_SNP_ID_22272908 m1A Human chr1 - 88992711 88992711 88992711 AGATCCTGGCCTACCCCTCCGCCAAAGCGCGCACTGAGTGCAAACCCCAGAGTCAATCCCTGTCC AGATCCTGGCCTACCCCTCCGCCAAAGCGCGCCCTGAGTGCAAACCCCAGAGTCAATCCCTGTCC T G KYAT3,RBMXL1 Ensembl:ENSG00000137944,Ensembl:ENSG00000213516 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:88992658..88992911 26863410 MeRIP-seq:(Medium) rs1331750384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364761,Human_RBP_ID_17338261,Human_RBP_ID_23418876 Human_Splice_Rec_94026 RMVar_hsa_circ_23721,RMVar_hsa_circ_92262,RMVar_hsa_circ_134408 66050 RMVar_ID_66050 Human_SNP_ID_22300409 m1A Human chr1 - 89103635 89103635 89103635 GACCCTTAAGCTTTTACATCTCTTAGCATGGAAGACGAAGAAAGCTGTACATTGTTGCTTGAGAG GACCCTTAAGCTTTTACATCTCTTAGCATGGAGGACGAAGAAAGCTGTACATTGTTGCTTGAGAG T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs922593400 Functional Loss SNV dbSNP153 33..33 33 - - - 66051 RMVar_ID_66051 Human_SNP_ID_22300656 m1A Human chr1 - 89104519 89104519 89104519 ATTTTATGTTGTTTACGAAAAGGAGAATCTGGACAGTCATGGCCAAGGTTAACAAAAGAAAGGGC ATTTTATGTTGTTTACGAAAAGGAGAATCTGGGCAGTCATGGCCAAGGTTAACAAAAGAAAGGGC T C PTGES3P1 Ensembl:ENSG00000234518 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879140598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1840880,Human_miRNA_ID_1855136 66052 RMVar_ID_66052 Human_SNP_ID_22300657 m1A Human chr1 - 89104519 89104519 89104519 ATTTTATGTTGTTTACGAAAAGGAGAATCTGGACAGTCATGGCCAAGGTTAACAAAAGAAAGGGC ATTTTATGTTGTTTACGAAAAGGAGAATCTGGCCAGTCATGGCCAAGGTTAACAAAAGAAAGGGC T G PTGES3P1 Ensembl:ENSG00000234518 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879140598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1840880,Human_miRNA_ID_1855136 66053 RMVar_ID_66053 Human_SNP_ID_22401782 m1A Human chr1 + 89524924 89524924 89524924 CGGGGCTTCCCGCTGAGCCCGCAGCCTCCGGCAGCCGGGAAAGTGCGGGCGCGGGGCCGCAGCCT CGGGGCTTCCCGCTGAGCCCGCAGCCTCCGGCCGCCGGGAAAGTGCGGGCGCGGGGCCGCAGCCT A C LRRC8B Ensembl:ENSG00000197147 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:89524873..89524972 26863196 MeRIP-seq:(Medium) rs1034470759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074168,Human_RBP_ID_22870877 Human_Splice_Rec_94455,Human_Splice_Rec_94465,Human_Splice_Rec_94481,Human_Splice_Rec_94493 66054 RMVar_ID_66054 Human_SNP_ID_22401783 m1A Human chr1 + 89524924 89524924 89524924 CGGGGCTTCCCGCTGAGCCCGCAGCCTCCGGCAGCCGGGAAAGTGCGGGCGCGGGGCCGCAGCCT CGGGGCTTCCCGCTGAGCCCGCAGCCTCCGGCGGCCGGGAAAGTGCGGGCGCGGGGCCGCAGCCT A G LRRC8B Ensembl:ENSG00000197147 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:89524873..89524972 26863196 MeRIP-seq:(Medium) rs1034470759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074168,Human_RBP_ID_22870877 Human_Splice_Rec_94455,Human_Splice_Rec_94465,Human_Splice_Rec_94481,Human_Splice_Rec_94493 66055 RMVar_ID_66055 Human_SNP_ID_22425876 m1A Human chr1 - 89633191 89633191 89633191 GGGTCGCTGCTCATGGCTTGTCGCGCCCGAGCACTGCGGCCGCGGCCACGGCGGCGCCTTCCTCC GGGTCGCTGCTCATGGCTTGTCGCGCCCGAGCGCTGCGGCCGCGGCCACGGCGGCGCCTTCCTCC T C LRRC8C-DT,LRRC8C-DT:2,LRRC8C-DT:3,LRRC8C-DT:4,LRRC8C-DT:5 RNACentral:URS0000D5C83E,RNACentral:URS0000D5C658,RNACentral:URS0000D5D4D7,RNACentral:URS0000D5AA1B,RNACentral:URS0000D59116 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:89633144..89633262 26863196 MeRIP-seq:(Medium) rs1183541455 Functional Loss SNV dbSNP153 33..33 33 - - - 66056 RMVar_ID_66056 Human_SNP_ID_22469397 m1A Human chr1 - 89821086 89821066 89821087 GGAGCCGGGGCACCACGGGCGGCGGCAGCGGCAGCGGCAGCAGCGGCGACGGGAGCAGCAGCACA GGAGCCGGGGCACCACGGGCGGCGGCAGCGG_____________________GAGCAGCAGCACA CCCGTCGCCGCTGCTGCCGCTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:89821035..89821206 26863196 MeRIP-seq:(Medium) rs1010514856 Functional Loss DEL dbSNP153 32..52 33 - - - 66057 RMVar_ID_66057 Human_SNP_ID_22469408 m1A Human chr1 - 89821086 89821086 89821086 GGAGCCGGGGCACCACGGGCGGCGGCAGCGGCAGCGGCAGCAGCGGCGACGGGAGCAGCAGCACA GGAGCCGGGGCACCACGGGCGGCGGCAGCGGCGGCGGCAGCAGCGGCGACGGGAGCAGCAGCACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:89821035..89821206 26863196 MeRIP-seq:(Medium) rs1331015240 Functional Loss SNV dbSNP153 33..33 33 - - - 66058 RMVar_ID_66058 Human_SNP_ID_22469412 m1A Human chr1 - 89821092 89821092 89821092 GGCGGAGGAGCCGGGGCACCACGGGCGGCGGCAGCGGCAGCGGCAGCAGCGGCGACGGGAGCAGC GGCGGAGGAGCCGGGGCACCACGGGCGGCGGCGGCGGCAGCGGCAGCAGCGGCGACGGGAGCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:89821050..89821198 26863196 MeRIP-seq:(Medium) rs111565421 Functional Loss SNV dbSNP153 33..33 33 - - - 66059 RMVar_ID_66059 Human_SNP_ID_22474772 m1A Human chr1 + 89843295 89843295 89843295 AAGGAAGAAAAAGAAGGCCGATCACACTGGGCACCGGCGGAGGAAGCGTGGAGTCCATTGATCTA AAGGAAGAAAAAGAAGGCCGATCACACTGGGCGCCGGCGGAGGAAGCGTGGAGTCCATTGATCTA A G AC093423.3,LRRC8D Ensembl:ENSG00000271949,Ensembl:ENSG00000171492 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:89843284..89843634 26863196 MeRIP-seq:(Medium) rs773364990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191402,Human_RBP_ID_3933679,Human_RBP_ID_8321251,Human_RBP_ID_9411936,Human_RBP_ID_18455164,Human_RBP_ID_22637164,Human_RBP_ID_22870879,Human_RBP_ID_24541680,Human_RBP_ID_26773113,Human_RBP_ID_27800505 66060 RMVar_ID_66060 Human_SNP_ID_22509319 m1A Human chr1 - 89994914 89994914 89994914 AAGGAGCGCTAAAGATTGGCGGGGGTTGTGGGAAAGCAAGCCGAGTGTACGGGAAGGGCCGGCTG AAGGAGCGCTAAAGATTGGCGGGGGTTGTGGGGAAGCAAGCCGAGTGTACGGGAAGGGCCGGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:89994866..89994951 26863196 MeRIP-seq:(Medium) rs1354731249 Functional Loss SNV dbSNP153 33..33 33 - - - 66061 RMVar_ID_66061 Human_SNP_ID_595681762 m1A Human chr16 - 15001734 15001734 15001734 AAAAAGAGTTGATGGGCTGATGGGAACAGCACACATCCCCCGCCACTCTCCCGCTACTTCCCTCA AAAAAGAGTTGATGGGCTGATGGGAACAGCACCCATCCCCCGCCACTCTCCCGCTACTTCCCTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15001728..15001799 26863196 MeRIP-seq:(Medium) rs758995289 Functional Loss SNV dbSNP153 33..33 33 - - - 66062 RMVar_ID_66062 Human_SNP_ID_595690639 m1A Human chr16 + 15028197 15028197 15028197 TGCCTCAGTCAGACCAGTCTTCTCCGCGCTCCAGAACACTCTGCCCTTTCCTACCGCAAGGGCTT TGCCTCAGTCAGACCAGTCTTCTCCGCGCTCCCGAACACTCTGCCCTTTCCTACCGCAAGGGCTT A C PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15027953..15028230 26863196 MeRIP-seq:(Medium) rs1487748054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8428123,Human_RBP_ID_12672122 Human_miRNA_ID_2793351,Human_miRNA_ID_2793352 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_69488,RMVar_hsa_circ_39291,RMVar_hsa_circ_328418,RMVar_hsa_circ_176507,RMVar_hsa_circ_370323,RMVar_hsa_circ_176508 66063 RMVar_ID_66063 Human_SNP_ID_595690640 m1A Human chr16 + 15028197 15028197 15028197 TGCCTCAGTCAGACCAGTCTTCTCCGCGCTCCAGAACACTCTGCCCTTTCCTACCGCAAGGGCTT TGCCTCAGTCAGACCAGTCTTCTCCGCGCTCCGGAACACTCTGCCCTTTCCTACCGCAAGGGCTT A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15027953..15028230 26863196 MeRIP-seq:(Medium) rs1487748054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8428123,Human_RBP_ID_12672122 Human_miRNA_ID_2793351,Human_miRNA_ID_2793352 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_69488,RMVar_hsa_circ_39291,RMVar_hsa_circ_328418,RMVar_hsa_circ_176507,RMVar_hsa_circ_370323,RMVar_hsa_circ_176508 66064 RMVar_ID_66064 Human_SNP_ID_595692533 m1A Human chr16 - 15033345 15033345 15033345 CGGGCTGTGGCCGCAATGGTCTCCACGAGCTCAGCAGCATCGACGTTGTCGCTCGCCATGCCGAC CGGGCTGTGGCCGCAATGGTCTCCACGAGCTCGGCAGCATCGACGTTGTCGCTCGCCATGCCGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15033296..15033445 26863196 MeRIP-seq:(Medium) rs902659863 Functional Loss SNV dbSNP153 33..33 33 - - - 66065 RMVar_ID_66065 Human_SNP_ID_595693593 m1A Human chr16 - 15036103 15036103 15036103 TGATCTGCTCCGGCCCACTGGATAGGCGCTCCACCTTTTCTAAGTCTTCAATGTGACTGACTGAG TGATCTGCTCCGGCCCACTGGATAGGCGCTCCGCCTTTTCTAAGTCTTCAATGTGACTGACTGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15036053..15036234 26863196 MeRIP-seq:(Medium) rs1166426969 Functional Loss SNV dbSNP153 33..33 33 - - - 66066 RMVar_ID_66066 Human_SNP_ID_595715073 m1A Human chr16 - 15104551 15104551 15104551 CCCTTCCACCCTCAGCGGATGATAATCTCAAGACACCTCCGAGTGTCTGCTCACTCCCCTTCCAC CCCTTCCACCCTCAGCGGATGATAATCTCAAGGCACCTCCGAGTGTCTGCTCACTCCCCTTCCAC T C NPIPP1 Ensembl:ENSG00000188599 Pseudogene exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:15104426..15104644 26863196 MeRIP-seq:(Medium) rs780803226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45898,Human_RBP_ID_468764,Human_RBP_ID_1512775,Human_RBP_ID_1838432,Human_RBP_ID_3510515,Human_RBP_ID_5096528,Human_RBP_ID_8428165,Human_RBP_ID_17079139,Human_RBP_ID_17252996,Human_RBP_ID_17373321,Human_RBP_ID_17884470,Human_RBP_ID_18673527,Human_RBP_ID_18941036,Human_RBP_ID_20169435,Human_RBP_ID_23679554 Human_miRNA_ID_1892607,Human_miRNA_ID_2866012,Human_miRNA_ID_2866013,Human_miRNA_ID_2866014,Human_miRNA_ID_2866015 RMVar_hsa_circ_78702,RMVar_hsa_circ_88288,RMVar_hsa_circ_107152,RMVar_hsa_circ_82833,RMVar_hsa_circ_176527,RMVar_hsa_circ_176528,RMVar_hsa_circ_176529,RMVar_hsa_circ_176526 66067 RMVar_ID_66067 Human_SNP_ID_595720627 m1A Human chr16 + 15123224 15123224 15123224 ACATTCCAAGTAGCGCCCGCATCATCCCAATGACCCCTCCCCCATCTCAGTCCCCCACGCTCCTC ACATTCCAAGTAGCGCCCGCATCATCCCAATGGCCCCTCCCCCATCTCAGTCCCCCACGCTCCTC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:15123218..15123326 26863196 MeRIP-seq:(Medium) rs1184414645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_39424 66068 RMVar_ID_66068 Human_SNP_ID_595720643 m1A Human chr16 + 15123262 15123262 15123262 CCCCCATCTCAGTCCCCCACGCTCCTCCCAAGACCAGGTCCTCTCTGGAACCTTCACAAACCTGA CCCCCATCTCAGTCCCCCACGCTCCTCCCAAGGCCAGGTCCTCTCTGGAACCTTCACAAACCTGA A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:15123244..15123335 26863196 MeRIP-seq:(Medium) rs1361250139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_39424 66069 RMVar_ID_66069 Human_SNP_ID_595722854 m1A Human chr16 + 15127847 15127847 15127847 GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCACTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCGCTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15127789..15128318 32194978 MeRIP-seq:(Medium) rs545460151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66070 RMVar_ID_66070 Human_SNP_ID_595722855 m1A Human chr16 + 15127847 15127847 15127847 GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCACTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCTCTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC A T PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15127789..15128318 32194978 MeRIP-seq:(Medium) rs545460151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66071 RMVar_ID_66071 Human_SNP_ID_595724964 m1A Human chr16 + 15131441 15131441 15131441 ACTGAGGTTAGCCGGGGCCCTGCTGAAAGCCTAGGGGATGGAGAAGTGGCAGCCAGGCCCTGGGG ACTGAGGTTAGCCGGGGCCCTGCTGAAAGCCTGGGGGATGGAGAAGTGGCAGCCAGGCCCTGGGG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15131439..15131589 32194978 MeRIP-seq:(Medium) rs1444831974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66072 RMVar_ID_66072 Human_SNP_ID_595728645 m1A Human chr16 + 15140812 15140810 15140813 CCTGGGCACCCCTCCTGGTCCCACGCACTCCCAGTAGTGCTCCTGGCACAGGGACTGTGGCTCCG CCTGGGCACCCCTCCTGGTCCCACGCACTCC___TAGTGCTCCTGGCACAGGGACTGTGGCTCCG CCAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15140792..15141186 26863196 MeRIP-seq:(Medium) rs1012231643 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66073 RMVar_ID_66073 Human_SNP_ID_595732109 m1A Human chr16 + 15149480 15149480 15149480 GCCCCTCCGTGGCCTGGCCAGCCCCCCAAGGAAGCTGTGTCTGTGGCAGTTGCGCTCTAAGGCAT GCCCCTCCGTGGCCTGGCCAGCCCCCCAAGGACGCTGTGTCTGTGGCAGTTGCGCTCTAAGGCAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:15149465..15149687 26863196 MeRIP-seq:(Medium) rs991324678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66074 RMVar_ID_66074 Human_SNP_ID_595733561 m1A Human chr16 + 15153859 15153859 15153859 CCTCACACCTCCCGTGGCCAGCCTCCAGCCTCATGGTCTTTGCTCACACCGTTCACCCCCCTTCT CCTCACACCTCCCGTGGCCAGCCTCCAGCCTCGTGGTCTTTGCTCACACCGTTCACCCCCCTTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15153840..15154308 26863196 MeRIP-seq:(Medium) rs938023417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66075 RMVar_ID_66075 Human_SNP_ID_595733640 m1A Human chr16 + 15153998 15153998 15153998 CCTCCTGGAACTCTTCCCTGCAGCCCCCTACAACCATCCCCACCTCTCCGGGTACCCCGCAGCCC CCTCCTGGAACTCTTCCCTGCAGCCCCCTACAGCCATCCCCACCTCTCCGGGTACCCCGCAGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:15153841..15154332;chr16:15153850..15154333 26863196 MeRIP-seq:(Medium) rs536510689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66076 RMVar_ID_66076 Human_SNP_ID_595734089 m1A Human chr16 + 15154712 15154712 15154712 GCCGCGACCTGCTGCTGAGCGACGCCCGCTCGAGGCTCGGGGCCAGGCCGCTCCGGGAGCTTGGC GCCGCGACCTGCTGCTGAGCGACGCCCGCTCGCGGCTCGGGGCCAGGCCGCTCCGGGAGCTTGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:15154661..15154752 26863196 MeRIP-seq:(Medium) rs561273071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66077 RMVar_ID_66077 Human_SNP_ID_595734090 m1A Human chr16 + 15154712 15154712 15154712 GCCGCGACCTGCTGCTGAGCGACGCCCGCTCGAGGCTCGGGGCCAGGCCGCTCCGGGAGCTTGGC GCCGCGACCTGCTGCTGAGCGACGCCCGCTCGGGGCTCGGGGCCAGGCCGCTCCGGGAGCTTGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:15154661..15154752 26863196 MeRIP-seq:(Medium) rs561273071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66078 RMVar_ID_66078 Human_SNP_ID_595734112 m1A Human chr16 - 15154741 15154741 15154741 GCACTGCAGCGCCAGCGTCCGAGCGGGCGGCCAAGCTCCCGGAGCGGCCTGGCCCCGAGCCTCGA GCACTGCAGCGCCAGCGTCCGAGCGGGCGGCCGAGCTCCCGGAGCGGCCTGGCCCCGAGCCTCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15154603..15154794 26863196 MeRIP-seq:(Medium) rs934099435 Functional Loss SNV dbSNP153 33..33 33 - - - 66079 RMVar_ID_66079 Human_SNP_ID_595780497 m1A Human chr16 + 15363788 15363788 15363788 GAGGGTGGAAGGGGAGTGAGCAGACACTCGGCAGGTGTCTTGAGATTATCATCCGCTGAGGGTAG GAGGGTGGAAGGGGAGTGAGCAGACACTCGGCGGGTGTCTTGAGATTATCATCCGCTGAGGGTAG A G HSALNG0109939-001 RNACentral:URS0000EAC10B lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:15363684..15363825 26863196 MeRIP-seq:(Medium) rs1190449593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66080 RMVar_ID_66080 Human_SNP_ID_595822440 m1A Human chr16 - 15517870 15517870 15517870 ACAGATCCACACACACACATCCACACACCCACACACATCCACACACACACATCCACAATACACAT ACAGATCCACACACACACATCCACACACCCACGCACATCCACACACACACATCCACAATACACAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:15517861..15518041 26863196 MeRIP-seq:(Medium) rs1325196662 Functional Loss SNV dbSNP153 33..33 33 - - - 66081 RMVar_ID_66081 Human_SNP_ID_595844846 m1A Human chr16 + 15596803 15596800 15596803 TTCCACGGGGTCCTTGCTGAGCAGTGACTCGGAGGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA TTCCACGGGGTCCTTGCTGAGCAGTGACTC___GGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA CGGA C BMERB1 Ensembl:ENSG00000166780 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15596752..15596841 26863196 MeRIP-seq:(Medium) rs761451573 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66082 RMVar_ID_66082 Human_SNP_ID_595844850 m1A Human chr16 + 15596803 15596803 15596803 TTCCACGGGGTCCTTGCTGAGCAGTGACTCGGAGGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA TTCCACGGGGTCCTTGCTGAGCAGTGACTCGGGGGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA A G BMERB1 Ensembl:ENSG00000166780 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15596752..15596841 26863196 MeRIP-seq:(Medium) rs1432095404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66083 RMVar_ID_66083 Human_SNP_ID_595851686 m1A Human chr16 - 15619460 15619460 15619460 GAATCATGCTGCAGGAAGACTCTTCTCGTAGCAGTGGTGTCTGAGAGGGCAGGAACAGGGGAGAG GAATCATGCTGCAGGAAGACTCTTCTCGTAGCGGTGGTGTCTGAGAGGGCAGGAACAGGGGAGAG T C MARF1 Ensembl:ENSG00000166783 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:15619409..15619503 26863196 MeRIP-seq:(Medium) rs1225956721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12673425 RMVar_hsa_circ_176553,RMVar_hsa_circ_125353,RMVar_hsa_circ_176550,RMVar_hsa_circ_176551,RMVar_hsa_circ_347986,RMVar_hsa_circ_368573,RMVar_hsa_circ_298197,RMVar_hsa_circ_312423,RMVar_hsa_circ_337373,RMVar_hsa_circ_308314,RMVar_hsa_circ_176555,RMVar_hsa_circ_176554 66084 RMVar_ID_66084 Human_SNP_ID_595857287 m1A Human chr16 + 15639232 15639232 15639232 TGCAGGAGTTCTCAGTTCCGTTTCCTTCCATCATACAGCCATGCAAAGTGATTCAACATCCTTTC TGCAGGAGTTCTCAGTTCCGTTTCCTTCCATCGTACAGCCATGCAAAGTGATTCAACATCCTTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:15639137..15639331 26863196 MeRIP-seq:(Medium) rs776045462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 66085 RMVar_ID_66085 Human_SNP_ID_595857297 m1A Human chr16 - 15639251 15639251 15639251 AATGAAAGAAAAGAAAGATGAAAGGATGTTGAATCACTTTGCATGGCTGTATGATGGAAGGAAAC AATGAAAGAAAAGAAAGATGAAAGGATGTTGAGTCACTTTGCATGGCTGTATGATGGAAGGAAAC T C MARF1 Ensembl:ENSG00000166783 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:15639200..15639328 26863196 MeRIP-seq:(Medium) rs373264834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891554,Human_RBP_ID_1838479,Human_RBP_ID_3947331,Human_RBP_ID_5465674,Human_RBP_ID_8186893,Human_RBP_ID_8941491,Human_RBP_ID_23679693,Human_RBP_ID_26329817,Human_RBP_ID_27810918 Human_Splice_Rec_1682138,Human_Splice_Rec_1682188,Human_Splice_Rec_1682244,Human_Splice_Rec_1682296,Human_Splice_Rec_1682424,Human_Splice_Rec_1682434 66086 RMVar_ID_66086 Human_SNP_ID_595857301 m1A Human chr16 - 15639261 15639261 15639261 AGGGTGGAAGAATGAAAGAAAAGAAAGATGAAAGGATGTTGAATCACTTTGCATGGCTGTATGAT AGGGTGGAAGAATGAAAGAAAAGAAAGATGAAGGGATGTTGAATCACTTTGCATGGCTGTATGAT T C MARF1 Ensembl:ENSG00000166783 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15639211..15639334 26863196 MeRIP-seq:(Medium) rs765414011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891554,Human_RBP_ID_1838479,Human_RBP_ID_3947331,Human_RBP_ID_8186893,Human_RBP_ID_8941491,Human_RBP_ID_23679694,Human_RBP_ID_26329817,Human_RBP_ID_27810918 Human_Splice_Rec_1682138,Human_Splice_Rec_1682188,Human_Splice_Rec_1682244,Human_Splice_Rec_1682296,Human_Splice_Rec_1682424,Human_Splice_Rec_1682434 66087 RMVar_ID_66087 Human_SNP_ID_595864639 m1A Human chr16 + 15664835 15664835 15664835 AGCTCCGAGGAGGAAGAAGCTAACTATTGGAAAGATCTGGCGATGACCTACAAACAGAGGTCAGT AGCTCCGAGGAGGAAGAAGCTAACTATTGGAAGGATCTGGCGATGACCTACAAACAGAGGTCAGT A G NDE1 Ensembl:ENSG00000072864 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15664760..15664903 26863196 MeRIP-seq:(Medium) rs1333403349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889485,Human_RBP_ID_4396201,Human_RBP_ID_5571461,Human_RBP_ID_9372346,Human_RBP_ID_26328703 Human_Splice_Rec_1682442,Human_Splice_Rec_1682443,Human_Splice_Rec_1682458,Human_Splice_Rec_1682459,Human_Splice_Rec_1682476,Human_Splice_Rec_1682477,Human_Splice_Rec_1682484,Human_Splice_Rec_1682485,Human_Splice_Rec_1682494,Human_Splice_Rec_1682495 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_20321,RMVar_hsa_circ_304453,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_332068,RMVar_hsa_circ_176566,RMVar_hsa_circ_331301,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176571,RMVar_hsa_circ_176572,RMVar_hsa_circ_176570,RMVar_hsa_circ_176568 66088 RMVar_ID_66088 Human_SNP_ID_595879856 m1A Human chr16 + 15712107 15712107 15712107 GACCACGAGGTTTGTGATGTGAATTGTTGGCAACTTCATCATTTTAGCTGCTGAGCTGGAGAGAG GACCACGAGGTTTGTGATGTGAATTGTTGGCACCTTCATCATTTTAGCTGCTGAGCTGGAGAGAG A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15712093..15712373 26863196 MeRIP-seq:(Medium) rs1299515642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565 66089 RMVar_ID_66089 Human_SNP_ID_595880037 m1A Human chr16 + 15712687 15712687 15712687 GATCAGCAGAGGAGAGGAAGAGGGACAACCCCACAGGTCGGGGGACAAGCAGGTGTGGATGGTGT GATCAGCAGAGGAGAGGAAGAGGGACAACCCCCCAGGTCGGGGGACAAGCAGGTGTGGATGGTGT A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15712654..15712740 26863196 MeRIP-seq:(Medium) rs12051525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565 66090 RMVar_ID_66090 Human_SNP_ID_595880314 m1A Human chr16 + 15713423 15713422 15713424 ATCATAAGTTCAAAGAAAAAGTGAAAAGCAGCAGAGAGTGAGAAGATGAGGGAGGGGTGTGGGAG ATCATAAGTTCAAAGAAAAAGTGAAAAGCAGC__AGAGTGAGAAGATGAGGGAGGGGTGTGGGAG CAG C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15713217..15713467 26863196 MeRIP-seq:(Medium) rs959844629 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565 66091 RMVar_ID_66091 Human_SNP_ID_595880315 m1A Human chr16 + 15713423 15713423 15713423 ATCATAAGTTCAAAGAAAAAGTGAAAAGCAGCAGAGAGTGAGAAGATGAGGGAGGGGTGTGGGAG ATCATAAGTTCAAAGAAAAAGTGAAAAGCAGCTGAGAGTGAGAAGATGAGGGAGGGGTGTGGGAG A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:15713217..15713467 26863196 MeRIP-seq:(Medium) rs1231150672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565 66092 RMVar_ID_66092 Human_SNP_ID_595946820 m1A Human chr16 + 15949700 15949650 15949700 CCGCCCGGTGCCCGCCGCCGCCCGCGCCAGCAACCGGGCCCGATCACCCGCCGCCCGGTGCCCGC _________________________________CCGGGCCCGATCACCCGCCGCCCGGTGCCCGC GCCGGGCCCGATCACCCGCCGCCCGGTGCCCGCCGCCGCCCGCGCCAGCAA G ABCC1 Ensembl:ENSG00000103222 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr16:15949651..15949800;chr16:15949655..15949772 26863196 MeRIP-seq:(Medium) rs1479028796 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4392887,Human_RBP_ID_9325889 Human_Splice_Rec_1683095,Human_Splice_Rec_1683157 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_78027,RMVar_hsa_circ_125227,RMVar_hsa_circ_176593,RMVar_hsa_circ_176594 66093 RMVar_ID_66093 Human_SNP_ID_595946829 m1A Human chr16 - 15949676 15949663 15949677 GGGCCCGGTTGCTGGCGCGGGCGGCGGCGGGCACCGGGCGGCGGGTGATCGGGCCCGGCTGCTGG GGGCCCGGTTGCTGGCGCGGGCGGCGGCGGG______________TGATCGGGCCCGGCTGCTGG ACCCGCCGCCCGGTG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:15949644..15949784 26863196 MeRIP-seq:(Medium) rs557646879 Functional Loss DEL dbSNP153 32..45 33 - - - 66094 RMVar_ID_66094 Human_SNP_ID_595946848 m1A Human chr16 + 15949700 15949700 15949700 CCGCCCGGTGCCCGCCGCCGCCCGCGCCAGCAACCGGGCCCGATCACCCGCCGCCCGGTGCCCGC CCGCCCGGTGCCCGCCGCCGCCCGCGCCAGCAGCCGGGCCCGATCACCCGCCGCCCGGTGCCCGC A G ABCC1 Ensembl:ENSG00000103222 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr16:15949651..15949800;chr16:15949655..15949772 26863196 MeRIP-seq:(Medium) rs1366388268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392887,Human_RBP_ID_9325889 Human_Splice_Rec_1683095,Human_Splice_Rec_1683157 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_78027,RMVar_hsa_circ_125227,RMVar_hsa_circ_176593,RMVar_hsa_circ_176594 66095 RMVar_ID_66095 Human_SNP_ID_595946874 m1A Human chr16 + 15949773 15949773 15949773 GCGCCACCGGCATGGCGCTCCGGGGCTTCTGCAGCGCCGATGGCTCCGACCCGCTCTGGGTACGT GCGCCACCGGCATGGCGCTCCGGGGCTTCTGCGGCGCCGATGGCTCCGACCCGCTCTGGGTACGT A G ABCC1 Ensembl:ENSG00000103222 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15949725..16007892 32194978 MeRIP-seq:(Medium) rs1220102099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392888,Human_RBP_ID_19073510,Human_RBP_ID_26810008 Human_Splice_Rec_1683095,Human_Splice_Rec_1683157 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_78027,RMVar_hsa_circ_125227,RMVar_hsa_circ_176593,RMVar_hsa_circ_176594 66096 RMVar_ID_66096 Human_SNP_ID_595961516 m1A Human chr16 - 16000855 16000855 16000855 AACTCAGGTACCTCATTTAAAAAGCTTCCTCCACACTCCCCAAACAACCTGCCCCCAACCTTTGC AACTCAGGTACCTCATTTAAAAAGCTTCCTCCGCACTCCCCAAACAACCTGCCCCCAACCTTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16000852..16000917 26863196 MeRIP-seq:(Medium) rs916528231 Functional Loss SNV dbSNP153 33..33 33 - - - 66097 RMVar_ID_66097 Human_SNP_ID_595962058 m1A Human chr16 + 16002901 16002901 16002901 GGTCGTATTTGGAATATATCTGGAAGAATGTAAGATGTTAGCAATGGTAGCTTGCCTGTAGGGTA GGTCGTATTTGGAATATATCTGGAAGAATGTAGGATGTTAGCAATGGTAGCTTGCCTGTAGGGTA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16002899..16003198 26863196 MeRIP-seq:(Medium) rs1460713408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_78027,RMVar_hsa_circ_125227,RMVar_hsa_circ_176593,RMVar_hsa_circ_176594 66098 RMVar_ID_66098 Human_SNP_ID_595962345 m1A Human chr16 + 16003816 16003816 16003816 AACTGGTGGGTGGGTGGATGGATGGATGGGTGAATGAATTGGTAGGTGGGTAGGGTGGATGGGTG AACTGGTGGGTGGGTGGATGGATGGATGGGTGGATGAATTGGTAGGTGGGTAGGGTGGATGGGTG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16003811..16004249 26863196 MeRIP-seq:(Medium) rs1281001608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_78027,RMVar_hsa_circ_125227,RMVar_hsa_circ_176593,RMVar_hsa_circ_176594 66099 RMVar_ID_66099 Human_SNP_ID_595963366 m1A Human chr16 - 16006889 16006877 16006889 CCACCATCATCATCACCATCGCCACCATCACCACCACCATCACCGCCACCGCCACCGCCACCGCC CCACCATCATCATCACCATCGCCACCATCACC____________GCCACCGCCACCGCCACCGCC CGGTGATGGTGGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16006884..16006988 26863196 MeRIP-seq:(Medium) rs1458953962 Functional Loss DEL dbSNP153 33..44 33 - - - 66100 RMVar_ID_66100 Human_SNP_ID_595963379 m1A Human chr16 - 16006886 16006886 16006886 CCATCATCATCACCATCGCCACCATCACCACCACCATCACCGCCACCGCCACCGCCACCGCCACC CCATCATCATCACCATCGCCACCATCACCACCGCCATCACCGCCACCGCCACCGCCACCGCCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16006882..16006974 26863196 MeRIP-seq:(Medium) rs1334239647 Functional Loss SNV dbSNP153 33..33 33 - - - 66101 RMVar_ID_66101 Human_SNP_ID_595963383 m1A Human chr16 - 16006889 16006889 16006889 CCACCATCATCATCACCATCGCCACCATCACCACCACCATCACCGCCACCGCCACCGCCACCGCC CCACCATCATCATCACCATCGCCACCATCACCTCCACCATCACCGCCACCGCCACCGCCACCGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16006884..16006988 26863196 MeRIP-seq:(Medium) rs926455193 Functional Loss SNV dbSNP153 33..33 33 - - - 66102 RMVar_ID_66102 Human_SNP_ID_595963384 m1A Human chr16 - 16006889 16006889 16006889 CCACCATCATCATCACCATCGCCACCATCACCACCACCATCACCGCCACCGCCACCGCCACCGCC CCACCATCATCATCACCATCGCCACCATCACCGCCACCATCACCGCCACCGCCACCGCCACCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16006884..16006988 26863196 MeRIP-seq:(Medium) rs926455193 Functional Loss SNV dbSNP153 33..33 33 - - - 66103 RMVar_ID_66103 Human_SNP_ID_595964842 m1A Human chr16 - 16011270 16011270 16011270 CACTGTTCACCCTGCTCAGAATGTCCTGCCTTAAACTTGTTCTCTCCTTTTTTTTTTCTTTTTCT CACTGTTCACCCTGCTCAGAATGTCCTGCCTTTAACTTGTTCTCTCCTTTTTTTTTTCTTTTTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16011268..16011407 26863196 MeRIP-seq:(Medium) rs1164027339 Functional Loss SNV dbSNP153 33..33 33 - - - 66104 RMVar_ID_66104 Human_SNP_ID_595966926 m1A Human chr16 + 16017943 16017943 16017943 GGGGAGGTGTGGAGAGAACAGCAAGAAAAGCCAGCACAGCAGGAGAAGGCTAAGAGACAGTGGGT GGGGAGGTGTGGAGAGAACAGCAAGAAAAGCCGGCACAGCAGGAGAAGGCTAAGAGACAGTGGGT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:16017831..16018092;chr16:16017939..16018033 26863196 MeRIP-seq:(Medium) rs537929356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_29597,RMVar_hsa_circ_279614,RMVar_hsa_circ_305639,RMVar_hsa_circ_351085,RMVar_hsa_circ_369671,RMVar_hsa_circ_373070,RMVar_hsa_circ_373728,RMVar_hsa_circ_370458,RMVar_hsa_circ_362371,RMVar_hsa_circ_340715,RMVar_hsa_circ_88994,RMVar_hsa_circ_64508,RMVar_hsa_circ_114958,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176602,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_116070,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609,RMVar_hsa_circ_340958,RMVar_hsa_circ_363403,RMVar_hsa_circ_45957,RMVar_hsa_circ_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_295625,RMVar_hsa_circ_176611,RMVar_hsa_circ_332712,RMVar_hsa_circ_269678,RMVar_hsa_circ_88330,RMVar_hsa_circ_176616,RMVar_hsa_circ_176618,RMVar_hsa_circ_37879,RMVar_hsa_circ_176619,RMVar_hsa_circ_176617 66105 RMVar_ID_66105 Human_SNP_ID_595972102 m1A Human chr16 + 16036599 16036599 16036599 TAAAGAACTGGAAGAAGGAATGCGCCAAGACTAGGAAGTAAGTGTGAGTTTCCTTGTCCTCCAGG TAAAGAACTGGAAGAAGGAATGCGCCAAGACTCGGAAGTAAGTGTGAGTTTCCTTGTCCTCCAGG A C ABCC1 Ensembl:ENSG00000103222 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:16033115..16044662 32194978 MeRIP-seq:(Medium) rs1337081313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889489,Human_RBP_ID_3948812,Human_RBP_ID_5524078,Human_RBP_ID_9372348,Human_RBP_ID_18985541,Human_RBP_ID_19073514,Human_RBP_ID_24551891,Human_RBP_ID_26328072,Human_RBP_ID_27811651 Human_Splice_Rec_1683107,Human_Splice_Rec_1683169,Human_Splice_Rec_1683225,Human_Splice_Rec_1683281 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_315,RMVar_hsa_circ_29597,RMVar_hsa_circ_279614,RMVar_hsa_circ_305639,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_373728,RMVar_hsa_circ_370458,RMVar_hsa_circ_362371,RMVar_hsa_circ_340715,RMVar_hsa_circ_88994,RMVar_hsa_circ_64508,RMVar_hsa_circ_114958,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_116070,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609,RMVar_hsa_circ_363403,RMVar_hsa_circ_45957,RMVar_hsa_circ_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_332712,RMVar_hsa_circ_269678,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_37879,RMVar_hsa_circ_176619,RMVar_hsa_circ_176617,RMVar_hsa_circ_301393,RMVar_hsa_circ_347337,RMVar_hsa_circ_370295,RMVar_hsa_circ_303867,RMVar_hsa_circ_17801,RMVar_hsa_circ_279065,RMVar_hsa_circ_15940,RMVar_hsa_circ_176625,RMVar_hsa_circ_106239,RMVar_hsa_circ_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621,RMVar_hsa_circ_106663,RMVar_hsa_circ_370894,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176627,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_176626 66106 RMVar_ID_66106 Human_SNP_ID_595973144 m1A Human chr16 + 16039854 16039854 16039854 GGGCTTTCCAGGTAGAGGGAGCAGCCAGTGCAAAGGCTCTGAGGACACTCGTGGTGCATCAGGGG GGGCTTTCCAGGTAGAGGGAGCAGCCAGTGCAGAGGCTCTGAGGACACTCGTGGTGCATCAGGGG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16039851..16040004 26863196 MeRIP-seq:(Medium) rs772400729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5647604 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_315,RMVar_hsa_circ_29597,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_373728,RMVar_hsa_circ_370458,RMVar_hsa_circ_362371,RMVar_hsa_circ_340715,RMVar_hsa_circ_88994,RMVar_hsa_circ_64508,RMVar_hsa_circ_114958,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_116070,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609,RMVar_hsa_circ_45957,RMVar_hsa_circ_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_269678,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_37879,RMVar_hsa_circ_176619,RMVar_hsa_circ_347337,RMVar_hsa_circ_370295,RMVar_hsa_circ_303867,RMVar_hsa_circ_17801,RMVar_hsa_circ_279065,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176621,RMVar_hsa_circ_106663,RMVar_hsa_circ_370894,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176627,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_176626 66107 RMVar_ID_66107 Human_SNP_ID_595987776 m1A Human chr16 - 16090541 16090541 16090541 CCTGCTCCTGCTCTGTGCTGGCATAGGTACGCAGGAACTCAGCGAAGGCGCCGTCTCGAGCCAGC CCTGCTCCTGCTCTGTGCTGGCATAGGTACGCGGGAACTCAGCGAAGGCGCCGTCTCGAGCCAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:16090490..16097994 32194978 MeRIP-seq:(Medium) rs748907288 Functional Loss SNV dbSNP153 33..33 33 - - - 66108 RMVar_ID_66108 Human_SNP_ID_595988099 m1A Human chr16 - 16091497 16091496 16091497 GGGTTTCCCTATCCCCTGCCTGAGTTGCCACAATGACACCCATCACTCCTCAGCCCATGGCATTG GGGTTTCCCTATCCCCTGCCTGAGTTGCCACA_TGACACCCATCACTCCTCAGCCCATGGCATTG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16091495..16091585 26863196 MeRIP-seq:(Medium) rs1479953457 Functional Loss DEL dbSNP153 33..33 33 - - - 66109 RMVar_ID_66109 Human_SNP_ID_595988100 m1A Human chr16 - 16091497 16091497 16091497 GGGTTTCCCTATCCCCTGCCTGAGTTGCCACAATGACACCCATCACTCCTCAGCCCATGGCATTG GGGTTTCCCTATCCCCTGCCTGAGTTGCCACAGTGACACCCATCACTCCTCAGCCCATGGCATTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16091495..16091585 26863196 MeRIP-seq:(Medium) rs552238756 Functional Loss SNV dbSNP153 33..33 33 - - - 66110 RMVar_ID_66110 Human_SNP_ID_595991373 m1A Human chr16 - 16102681 16102681 16102681 GCAGTTGCTTCCCTGCACTGTCCGTCACCAGCATGCCATTCTCCATTTGCTTTGCTTCCTTCCCT GCAGTTGCTTCCCTGCACTGTCCGTCACCAGCGTGCCATTCTCCATTTGCTTTGCTTCCTTCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:16102633..16102738 26863196 MeRIP-seq:(Medium) rs1363872336 Functional Loss SNV dbSNP153 33..33 33 - - - 66111 RMVar_ID_66111 Human_SNP_ID_595993241 m1A Human chr16 + 16106785 16106785 16106785 CTCCTCCTATAGTGGGGACATCAGCAGGCACCACAACAGCACCGCAGAACTGCAGAAAGCTGAGG CTCCTCCTATAGTGGGGACATCAGCAGGCACCCCAACAGCACCGCAGAACTGCAGAAAGCTGAGG A C ABCC1 Ensembl:ENSG00000103222 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:16106728..16106837 26863196 MeRIP-seq:(Medium) rs1478950298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22653937,Human_RBP_ID_24558850,Human_RBP_ID_25240894 Human_Splice_Rec_1683136,Human_Splice_Rec_1683137,Human_Splice_Rec_1683196,Human_Splice_Rec_1683197,Human_Splice_Rec_1683254,Human_Splice_Rec_1683255,Human_Splice_Rec_1683302,Human_Splice_Rec_1683303,Human_Splice_Rec_1683310,Human_Splice_Rec_1683314,Human_Splice_Rec_1683315,Human_Splice_Rec_1683319 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_373070,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_94162,RMVar_hsa_circ_176629,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_126019,RMVar_hsa_circ_176637,RMVar_hsa_circ_87122,RMVar_hsa_circ_103635,RMVar_hsa_circ_176636,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_176651,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_112258,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_176661,RMVar_hsa_circ_79706,RMVar_hsa_circ_268855,RMVar_hsa_circ_305130,RMVar_hsa_circ_78564,RMVar_hsa_circ_2985,RMVar_hsa_circ_176664,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_65241,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_284479,RMVar_hsa_circ_79504,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176669,RMVar_hsa_circ_176670,RMVar_hsa_circ_176667 66112 RMVar_ID_66112 Human_SNP_ID_596000797 m1A Human chr16 + 16131508 16131508 16131508 GGTGTGGGAGACAGAATACACTCAAGCATGCGAGCCCCAAGAGGGCTGGGGACAGGCAGTGCCCT GGTGTGGGAGACAGAATACACTCAAGCATGCGGGCCCCAAGAGGGCTGGGGACAGGCAGTGCCCT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16131504..16131625 26863196 MeRIP-seq:(Medium) rs375118845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_176630,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_126661,RMVar_hsa_circ_176666,RMVar_hsa_circ_176667,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_1870,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_3856,RMVar_hsa_circ_31156,RMVar_hsa_circ_319841,RMVar_hsa_circ_96886,RMVar_hsa_circ_176678,RMVar_hsa_circ_309340,RMVar_hsa_circ_372373,RMVar_hsa_circ_176682,RMVar_hsa_circ_176683,RMVar_hsa_circ_176681,RMVar_hsa_circ_372443,RMVar_hsa_circ_176685 66113 RMVar_ID_66113 Human_SNP_ID_596004121 m1A Human chr16 + 16141416 16141415 16141417 AAACATAAAAACCAAACCCAGACAACCAAAACATATTCAAAGCAGCAGCCACCGCCATCCGGTCC AAACATAAAAACCAAACCCAGACAACCAAAAC__ATTCAAAGCAGCAGCCACCGCCATCCGGTCC CAT C ABCC1 Ensembl:ENSG00000103222 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:16141366..16141514 26863196 MeRIP-seq:(Medium) rs1380369939 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_20093431,Human_RBP_ID_27439290 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_176687 66114 RMVar_ID_66114 Human_SNP_ID_596004122 m1A Human chr16 + 16141416 16141416 16141416 AAACATAAAAACCAAACCCAGACAACCAAAACATATTCAAAGCAGCAGCCACCGCCATCCGGTCC AAACATAAAAACCAAACCCAGACAACCAAAACTTATTCAAAGCAGCAGCCACCGCCATCCGGTCC A T ABCC1 Ensembl:ENSG00000103222 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:16141366..16141514 26863196 MeRIP-seq:(Medium) rs1361023902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20093431,Human_RBP_ID_27439290 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_176687 66115 RMVar_ID_66115 Human_SNP_ID_596004134 m1A Human chr16 - 16141467 16141467 16141467 GTGGTTCGCATCTCTGTCTCTCCTGGGTCTTCACAGCCAGTTCCAGGCAGGGGACCGGATGGCGG GTGGTTCGCATCTCTGTCTCTCCTGGGTCTTCGCAGCCAGTTCCAGGCAGGGGACCGGATGGCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:16141416..16141502 26863196 MeRIP-seq:(Medium) rs1467563550 Functional Loss SNV dbSNP153 33..33 33 - - - 66116 RMVar_ID_66116 Human_SNP_ID_596028975 m1A Human chr16 - 16232541 16232541 16232541 GACAGCCCAGGCCCCGCCCCACCGCCGCCGCCAGCCGCCGCCGCGCACGCGCGCTTCGACCCCAC GACAGCCCAGGCCCCGCCCCACCGCCGCCGCCTGCCGCCGCCGCGCACGCGCGCTTCGACCCCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16232526..16232598 26863196 MeRIP-seq:(Medium) rs1388599817 Functional Loss SNV dbSNP153 33..33 33 - - - 66117 RMVar_ID_66117 Human_SNP_ID_596028976 m1A Human chr16 - 16232541 16232541 16232541 GACAGCCCAGGCCCCGCCCCACCGCCGCCGCCAGCCGCCGCCGCGCACGCGCGCTTCGACCCCAC GACAGCCCAGGCCCCGCCCCACCGCCGCCGCCGGCCGCCGCCGCGCACGCGCGCTTCGACCCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16232526..16232598 26863196 MeRIP-seq:(Medium) rs1388599817 Functional Loss SNV dbSNP153 33..33 33 - - - 66118 RMVar_ID_66118 Human_SNP_ID_596196947 m1A Human chr16 + 17037166 17037166 17037166 AGGAAAGAGTAACTGCAAAGTCCAGAGGAGGGAAAGAACTTCTTGTATTCAGGGATCAGAAAAGA AGGAAAGAGTAACTGCAAAGTCCAGAGGAGGGCAAGAACTTCTTGTATTCAGGGATCAGAAAAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:17037115..17037235 26863196 MeRIP-seq:(Medium) rs950216942 Functional Loss SNV dbSNP153 33..33 33 - - - 66119 RMVar_ID_66119 Human_SNP_ID_596540918 m1A Human chr16 - 18557788 18557788 18557788 GATTTCTGTTTTCCTTCCTTCCTTTCCAGATAAAGCTGTACACCAAGCATGGGACTTTGAAATAC GATTTCTGTTTTCCTTCCTTCCTTTCCAGATAGAGCTGTACACCAAGCATGGGACTTTGAAATAC T C NOMO2 Ensembl:ENSG00000185164 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:18557780..18557907 26863196 MeRIP-seq:(Medium) rs767971568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17883392 Human_Splice_Rec_1684576,Human_Splice_Rec_1684577,Human_Splice_Rec_1684650,Human_Splice_Rec_1684651,Human_Splice_Rec_1684712,Human_Splice_Rec_1684713,Human_Splice_Rec_1684774,Human_Splice_Rec_1684775,Human_Splice_Rec_1684834,Human_Splice_Rec_1684835,Human_Splice_Rec_1684896,Human_Splice_Rec_1684897,Human_Splice_Rec_1684986,Human_Splice_Rec_1684987 RMVar_hsa_circ_13105,RMVar_hsa_circ_103236,RMVar_hsa_circ_176764,RMVar_hsa_circ_95878,RMVar_hsa_circ_176768 66120 RMVar_ID_66120 Human_SNP_ID_596541997 m1A Human chr16 + 18561973 18561971 18561974 CCTCCGAGCCGTGCGCCGGCCCCACGCCGCTCAGCAGCAGCACCACCGCGGCGGTGACCACCGCG CCTCCGAGCCGTGCGCCGGCCCCACGCCGCT___CAGCAGCACCACCGCGGCGGTGACCACCGCG TCAG T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:18561876..18562075 26863410 MeRIP-seq:(Medium) rs1225158110 Functional Loss DEL dbSNP153 32..34 33 - - - 66121 RMVar_ID_66121 Human_SNP_ID_596542023 m1A Human chr16 + 18562015 18562015 18562015 CCACCGCGGCGGTGACCACCGCGGGCCCCAGCAGCCCCGCGCCCTGGCCCACCAGCATGGCCCGA CCACCGCGGCGGTGACCACCGCGGGCCCCAGCGGCCCCGCGCCCTGGCCCACCAGCATGGCCCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:18561964..18562075;chr16:18561902..18562050;chr16:18561939..18562100;chr16:18561969..18562075;chr16:18561951..18562075;chr16:18561956..18562075 26863196 MeRIP-seq:(Medium) rs1161065393 Functional Loss SNV dbSNP153 33..33 33 - - - 66122 RMVar_ID_66122 Human_SNP_ID_596589336 m1A Human chr16 - 18788112 18788112 18788112 AGGTTACATTGGCGAATTTGAAATCATTGATGACCACAGAGCTGGGAAAATTGTTGTGAACCTCA AGGTTACATTGGCGAATTTGAAATCATTGATGGCCACAGAGCTGGGAAAATTGTTGTGAACCTCA T C RPS15A,AC138811.2 Ensembl:ENSG00000134419,Ensembl:ENSG00000260342 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:18788021..18788159 26863196 MeRIP-seq:(Medium) rs1333876924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277269,Human_RBP_ID_469283,Human_RBP_ID_1003134,Human_RBP_ID_1177191,Human_RBP_ID_1513313,Human_RBP_ID_1838738,Human_RBP_ID_3492008,Human_RBP_ID_4353178,Human_RBP_ID_8428683,Human_RBP_ID_8805012,Human_RBP_ID_9060494,Human_RBP_ID_12679308,Human_RBP_ID_17652932,Human_RBP_ID_17872483,Human_RBP_ID_18674097,Human_RBP_ID_22441808,Human_RBP_ID_22497254,Human_RBP_ID_22800017,Human_RBP_ID_23209270,Human_RBP_ID_23681067,Human_RBP_ID_26939270,Human_RBP_ID_27237675 Human_Splice_Rec_1685040,Human_Splice_Rec_1685041,Human_Splice_Rec_1685048,Human_Splice_Rec_1685049,Human_Splice_Rec_1685058,Human_Splice_Rec_1685059,Human_Splice_Rec_1685070,Human_Splice_Rec_1685071,Human_Splice_Rec_1685079,Human_Splice_Rec_1685086,Human_Splice_Rec_1685087,Human_Splice_Rec_1685094,Human_Splice_Rec_1685095,Human_Splice_Rec_1685104,Human_Splice_Rec_1685105,Human_Splice_Rec_1685114,Human_Splice_Rec_1685115,Human_Splice_Rec_1685130 RMVar_hsa_circ_122283,RMVar_hsa_circ_176773,RMVar_hsa_circ_77194,RMVar_hsa_circ_176774,RMVar_hsa_circ_119099,RMVar_hsa_circ_176777,RMVar_hsa_circ_375183,RMVar_hsa_circ_374711,RMVar_hsa_circ_176778,RMVar_hsa_circ_176779 66123 RMVar_ID_66123 Human_SNP_ID_596592285 m1A Human chr16 - 18798799 18798799 18798799 GCAGAGACTGCAAGTCTGGAAGAACAGCTGCAAGGATGGGGAGAAGTGATGCTGATGGCTGATAA GCAGAGACTGCAAGTCTGGAAGAACAGCTGCAGGGATGGGGAGAAGTGATGCTGATGGCTGATAA T C ARL6IP1,AC138811.2 Ensembl:ENSG00000170540,Ensembl:ENSG00000260342 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:18798751..18798873;chr16:18798751..18798850 26863196 MeRIP-seq:(Medium) rs930529794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469373,Human_RBP_ID_1513369,Human_RBP_ID_1838775,Human_RBP_ID_2469649,Human_RBP_ID_4394440,Human_RBP_ID_5359783,Human_RBP_ID_6496913,Human_RBP_ID_9353189,Human_RBP_ID_12679630,Human_RBP_ID_18674121,Human_RBP_ID_22441338,Human_RBP_ID_23113989,Human_RBP_ID_23681155,Human_RBP_ID_27237718 Human_Splice_Rec_1685120,Human_Splice_Rec_1685121,Human_Splice_Rec_1685132,Human_Splice_Rec_1685133,Human_Splice_Rec_1685142,Human_Splice_Rec_1685143,Human_Splice_Rec_1685150,Human_Splice_Rec_1685151,Human_Splice_Rec_1685160,Human_Splice_Rec_1685161,Human_Splice_Rec_1685164,Human_Splice_Rec_1685165,Human_Splice_Rec_1685172,Human_Splice_Rec_1685173,Human_Splice_Rec_1685178,Human_Splice_Rec_1685179,Human_Splice_Rec_1685182 Human_miRNA_ID_2013475,Human_miRNA_ID_2490648,Human_miRNA_ID_2752734,Human_miRNA_ID_2759867 RMVar_hsa_circ_113542,RMVar_hsa_circ_269859,RMVar_hsa_circ_176780,RMVar_hsa_circ_88782,RMVar_hsa_circ_117929,RMVar_hsa_circ_176782,RMVar_hsa_circ_176783,RMVar_hsa_circ_176785,RMVar_hsa_circ_176784,RMVar_hsa_circ_273718 66124 RMVar_ID_66124 Human_SNP_ID_596602206 m1A Human chr16 - 18836503 18836503 18836503 TAGGTATTCTGAGCACACCCAACTACAGACTCAGCAAAGAGCTGTTCAGGAAGCAATCCAGGTGA TAGGTATTCTGAGCACACCCAACTACAGACTCGGCAAAGAGCTGTTCAGGAAGCAATCCAGGTGA T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:18836452..18837273 32194978 MeRIP-seq:(Medium) rs1376955150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5695,Human_RBP_ID_5465687,Human_RBP_ID_5524149,Human_RBP_ID_18674176,Human_RBP_ID_26328725,Human_RBP_ID_27810930 Human_Splice_Rec_1685274,Human_Splice_Rec_1685390 Human_miRNA_ID_2947793 RMVar_hsa_circ_1659,RMVar_hsa_circ_3052,RMVar_hsa_circ_117787,RMVar_hsa_circ_176791,RMVar_hsa_circ_82048,RMVar_hsa_circ_97470,RMVar_hsa_circ_176792,RMVar_hsa_circ_176793,RMVar_hsa_circ_84851,RMVar_hsa_circ_176794,RMVar_hsa_circ_364098,RMVar_hsa_circ_74302,RMVar_hsa_circ_176795,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825,RMVar_hsa_circ_265632,RMVar_hsa_circ_65641,RMVar_hsa_circ_77120,RMVar_hsa_circ_274440,RMVar_hsa_circ_68179,RMVar_hsa_circ_46419,RMVar_hsa_circ_176809,RMVar_hsa_circ_18247,RMVar_hsa_circ_176810,RMVar_hsa_circ_176808,RMVar_hsa_circ_339731,RMVar_hsa_circ_57927,RMVar_hsa_circ_101069,RMVar_hsa_circ_122848,RMVar_hsa_circ_176815,RMVar_hsa_circ_176817,RMVar_hsa_circ_104967,RMVar_hsa_circ_176818,RMVar_hsa_circ_294681,RMVar_hsa_circ_63474,RMVar_hsa_circ_105242,RMVar_hsa_circ_16004,RMVar_hsa_circ_52921,RMVar_hsa_circ_176819,RMVar_hsa_circ_283394,RMVar_hsa_circ_335675,RMVar_hsa_circ_279533,RMVar_hsa_circ_85916,RMVar_hsa_circ_94673,RMVar_hsa_circ_52537,RMVar_hsa_circ_106330,RMVar_hsa_circ_176821,RMVar_hsa_circ_176823,RMVar_hsa_circ_176824,RMVar_hsa_circ_176825,RMVar_hsa_circ_176822,RMVar_hsa_circ_116646,RMVar_hsa_circ_176820,RMVar_hsa_circ_271469,RMVar_hsa_circ_112110,RMVar_hsa_circ_176829,RMVar_hsa_circ_103637,RMVar_hsa_circ_58045,RMVar_hsa_circ_176830,RMVar_hsa_circ_176827,RMVar_hsa_circ_176828,RMVar_hsa_circ_176826 66125 RMVar_ID_66125 Human_SNP_ID_596602657 m1A Human chr16 + 18838122 18838122 18838122 TCGGCCTGCTGGCCACCTCCACCATAGACAGCACCAGCAAACCCAGCCTCGCCTCCTGCTGTCCA TCGGCCTGCTGGCCACCTCCACCATAGACAGCGCCAGCAAACCCAGCCTCGCCTCCTGCTGTCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:18838071..18838163 26863196 MeRIP-seq:(Medium) rs1253533818 Functional Loss SNV dbSNP153 33..33 33 - - - 66126 RMVar_ID_66126 Human_SNP_ID_596605404 m1A Human chr16 - 18847530 18847530 18847530 GATGAGCTCTGGCTGGGAGTTTTGCTGCAACAACACATGTATGTCCTGAGACGAATTCAGCAGCT GATGAGCTCTGGCTGGGAGTTTTGCTGCAACAGCACATGTATGTCCTGAGACGAATTCAGCAGCT T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:18847479..18847811 32194978 MeRIP-seq:(Medium) rs372198549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066246,Human_RBP_ID_1513423,Human_RBP_ID_1838910,Human_RBP_ID_3948853,Human_RBP_ID_5524168,Human_RBP_ID_8805122,Human_RBP_ID_9373930,Human_RBP_ID_26329844 Human_Splice_Rec_1685256,Human_Splice_Rec_1685257,Human_Splice_Rec_1685372,Human_Splice_Rec_1685373,Human_Splice_Rec_1685432,Human_Splice_Rec_1685433 Human_miRNA_ID_1470233,Human_miRNA_ID_2627261,Human_miRNA_ID_2748092 RMVar_hsa_circ_117787,RMVar_hsa_circ_82048,RMVar_hsa_circ_176792,RMVar_hsa_circ_176793,RMVar_hsa_circ_84851,RMVar_hsa_circ_176794,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825,RMVar_hsa_circ_65641,RMVar_hsa_circ_77120,RMVar_hsa_circ_176808,RMVar_hsa_circ_63474,RMVar_hsa_circ_105242,RMVar_hsa_circ_16004,RMVar_hsa_circ_335675,RMVar_hsa_circ_85916,RMVar_hsa_circ_94673,RMVar_hsa_circ_21773,RMVar_hsa_circ_106330,RMVar_hsa_circ_176823,RMVar_hsa_circ_176824,RMVar_hsa_circ_176825,RMVar_hsa_circ_176822,RMVar_hsa_circ_116646,RMVar_hsa_circ_112110,RMVar_hsa_circ_176829,RMVar_hsa_circ_103637,RMVar_hsa_circ_176827,RMVar_hsa_circ_176828,RMVar_hsa_circ_176826,RMVar_hsa_circ_116891,RMVar_hsa_circ_357136,RMVar_hsa_circ_322308,RMVar_hsa_circ_176834,RMVar_hsa_circ_100818,RMVar_hsa_circ_176833,RMVar_hsa_circ_377357,RMVar_hsa_circ_95269,RMVar_hsa_circ_28839,RMVar_hsa_circ_35676,RMVar_hsa_circ_176837,RMVar_hsa_circ_289562,RMVar_hsa_circ_351053,RMVar_hsa_circ_108986,RMVar_hsa_circ_176838,RMVar_hsa_circ_176840,RMVar_hsa_circ_31934,RMVar_hsa_circ_176841,RMVar_hsa_circ_176839,RMVar_hsa_circ_113316,RMVar_hsa_circ_87823,RMVar_hsa_circ_176845,RMVar_hsa_circ_176844,RMVar_hsa_circ_377090,RMVar_hsa_circ_280366,RMVar_hsa_circ_116579,RMVar_hsa_circ_267701,RMVar_hsa_circ_327588,RMVar_hsa_circ_106160,RMVar_hsa_circ_176846,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_176847 66127 RMVar_ID_66127 Human_SNP_ID_596605405 m1A Human chr16 - 18847530 18847530 18847530 GATGAGCTCTGGCTGGGAGTTTTGCTGCAACAACACATGTATGTCCTGAGACGAATTCAGCAGCT GATGAGCTCTGGCTGGGAGTTTTGCTGCAACACCACATGTATGTCCTGAGACGAATTCAGCAGCT T G SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:18847479..18847811 32194978 MeRIP-seq:(Medium) rs372198549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066246,Human_RBP_ID_1513423,Human_RBP_ID_1838910,Human_RBP_ID_3948853,Human_RBP_ID_5524168,Human_RBP_ID_8805122,Human_RBP_ID_9373930,Human_RBP_ID_26329844 Human_Splice_Rec_1685256,Human_Splice_Rec_1685257,Human_Splice_Rec_1685372,Human_Splice_Rec_1685373,Human_Splice_Rec_1685432,Human_Splice_Rec_1685433 Human_miRNA_ID_1470233,Human_miRNA_ID_2627261,Human_miRNA_ID_2748092 RMVar_hsa_circ_117787,RMVar_hsa_circ_82048,RMVar_hsa_circ_176792,RMVar_hsa_circ_176793,RMVar_hsa_circ_84851,RMVar_hsa_circ_176794,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825,RMVar_hsa_circ_65641,RMVar_hsa_circ_77120,RMVar_hsa_circ_176808,RMVar_hsa_circ_63474,RMVar_hsa_circ_105242,RMVar_hsa_circ_16004,RMVar_hsa_circ_335675,RMVar_hsa_circ_85916,RMVar_hsa_circ_94673,RMVar_hsa_circ_21773,RMVar_hsa_circ_106330,RMVar_hsa_circ_176823,RMVar_hsa_circ_176824,RMVar_hsa_circ_176825,RMVar_hsa_circ_176822,RMVar_hsa_circ_116646,RMVar_hsa_circ_112110,RMVar_hsa_circ_176829,RMVar_hsa_circ_103637,RMVar_hsa_circ_176827,RMVar_hsa_circ_176828,RMVar_hsa_circ_176826,RMVar_hsa_circ_116891,RMVar_hsa_circ_357136,RMVar_hsa_circ_322308,RMVar_hsa_circ_176834,RMVar_hsa_circ_100818,RMVar_hsa_circ_176833,RMVar_hsa_circ_377357,RMVar_hsa_circ_95269,RMVar_hsa_circ_28839,RMVar_hsa_circ_35676,RMVar_hsa_circ_176837,RMVar_hsa_circ_289562,RMVar_hsa_circ_351053,RMVar_hsa_circ_108986,RMVar_hsa_circ_176838,RMVar_hsa_circ_176840,RMVar_hsa_circ_31934,RMVar_hsa_circ_176841,RMVar_hsa_circ_176839,RMVar_hsa_circ_113316,RMVar_hsa_circ_87823,RMVar_hsa_circ_176845,RMVar_hsa_circ_176844,RMVar_hsa_circ_377090,RMVar_hsa_circ_280366,RMVar_hsa_circ_116579,RMVar_hsa_circ_267701,RMVar_hsa_circ_327588,RMVar_hsa_circ_106160,RMVar_hsa_circ_176846,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_176847 66128 RMVar_ID_66128 Human_SNP_ID_596627939 m1A Human chr16 - 18925984 18925984 18925984 GGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCGCGGAGCTGGAATGACTGGCAACCC GGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCGAGTATCCGCGGAGCTGGAATGACTGGCAACCC T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:18925972..18926117 26863196 MeRIP-seq:(Medium) rs975189123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234950,Human_RBP_ID_1130555,Human_RBP_ID_4396597,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 66129 RMVar_ID_66129 Human_SNP_ID_596627942 m1A Human chr16 - 18925987 18925987 18925987 CTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCGCGGAGCTGGAATGACTGGCAA CTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCGCCAAGTATCCGCGGAGCTGGAATGACTGGCAA T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:18925951..18926388;chr16:18925953..18926071 26863196 MeRIP-seq:(Medium) rs574046661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234950,Human_RBP_ID_1130555,Human_RBP_ID_4396597,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 66130 RMVar_ID_66130 Human_SNP_ID_596627959 m1A Human chr16 - 18926008 18926002 18926008 TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGC______GGCGGCGGCGGCGGCACCAAGTATCCG CGCCGCT C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:18925959..18926367 26863196 MeRIP-seq:(Medium) rs770961779 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_234950,Human_RBP_ID_762716,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 66131 RMVar_ID_66131 Human_SNP_ID_596627964 m1A Human chr16 - 18926008 18926005 18926008 TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGC___GGCGGCGGCGGCGGCGGCACCAAGTATCCG CGCT C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:18925959..18926367 26863196 MeRIP-seq:(Medium) rs773997323 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_234950,Human_RBP_ID_762716,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 66132 RMVar_ID_66132 Human_SNP_ID_596627966 m1A Human chr16 - 18926008 18926008 18926008 TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCGGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:18925959..18926367 26863196 MeRIP-seq:(Medium) rs190057031 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_234950,Human_RBP_ID_762716,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 66133 RMVar_ID_66133 Human_SNP_ID_596628068 m1A Human chr16 + 18926183 18926171 18926183 CCGAGAAGGAGGAGGAGGAGGAGGAGGAGGAGAAGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA CCGAGAAGGAGGAGGAGGAGG____________AGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA GAGGAGGAGGAGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:18926071..18926351 26863196 MeRIP-seq:(Medium) rs928804377 Functional Loss DEL dbSNP153 22..33 33 - - - 66134 RMVar_ID_66134 Human_SNP_ID_596628074 m1A Human chr16 + 18926183 18926177 18926183 CCGAGAAGGAGGAGGAGGAGGAGGAGGAGGAGAAGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA CCGAGAAGGAGGAGGAGGAGGAGGAGG______AGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA GAGGAGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:18926071..18926351 26863196 MeRIP-seq:(Medium) rs1316356664 Functional Loss DEL dbSNP153 28..33 33 - - - 66135 RMVar_ID_66135 Human_SNP_ID_596628081 m1A Human chr16 + 18926183 18926180 18926183 CCGAGAAGGAGGAGGAGGAGGAGGAGGAGGAGAAGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA CCGAGAAGGAGGAGGAGGAGGAGGAGGAGG___AGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA GAGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:18926071..18926351 26863196 MeRIP-seq:(Medium) rs1301033883 Functional Loss DEL dbSNP153 31..33 33 - - - 66136 RMVar_ID_66136 Human_SNP_ID_596628085 m1A Human chr16 + 18926183 18926183 18926183 CCGAGAAGGAGGAGGAGGAGGAGGAGGAGGAGAAGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA CCGAGAAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGGAGGGCGGGGGAAGAGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:18926071..18926351 26863196 MeRIP-seq:(Medium) rs1333202002 Functional Loss SNV dbSNP153 33..33 33 - - - 66137 RMVar_ID_66137 Human_SNP_ID_596628110 m1A Human chr16 - 18926222 18926222 18926222 GTCCTGCGCTGCGGGCTCAGGCGGAACCCGGAACGGCCGTCCTCTTCCCCCGCCCTCCGCCGCCT GTCCTGCGCTGCGGGCTCAGGCGGAACCCGGAGCGGCCGTCCTCTTCCCCCGCCCTCCGCCGCCT T C SMG1 Ensembl:ENSG00000157106 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr16:18926139..18926360;chr16:18926178..18926346 26863196 MeRIP-seq:(Medium) rs1395271476 Functional Loss SNV dbSNP153 33..33 33 - - - 66138 RMVar_ID_66138 Human_SNP_ID_596628128 m1A Human chr16 + 18926278 18926276 18926278 GCGCAGGACGAGGAGGCGGGAGCGGCGCGGTGAGAGAGAGGCGGATGAAGGGGAGGCGACGTCTT GCGCAGGACGAGGAGGCGGGAGCGGCGCGGT__GAGAGAGGCGGATGAAGGGGAGGCGACGTCTT TGA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:18926228..18926344 32194978 MeRIP-seq:(Medium) rs888214614 Functional Loss DEL dbSNP153 32..33 33 - - - 66139 RMVar_ID_66139 Human_SNP_ID_596628538 m1A Human chr16 + 18927393 18927390 18927394 AAAGAGAGAGAGAAAGGAGGGAGGGAAGAAAAAGGAAGGAAGGAAGGGAGGAAGGAAGGAAAGGA AAAGAGAGAGAGAAAGGAGGGAGGGAAGAA____GAAGGAAGGAAGGGAGGAAGGAAGGAAAGGA AAAAG A AC092287.1 Ensembl:ENSG00000260352 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:18927352..18927437 26863196 MeRIP-seq:(Medium) rs956336020 Functional Loss DEL dbSNP153 31..34 33 - - - 66140 RMVar_ID_66140 Human_SNP_ID_596650811 m1A Human chr16 + 19009217 19009217 19009217 AGACTCCAGTTGCTTCTCTTCTCCACCTGTGAACTTCCTCCAAGAATTGCCAAGCTACCGGTCCA AGACTCCAGTTGCTTCTCTTCTCCACCTGTGAGCTTCCTCCAAGAATTGCCAAGCTACCGGTCCA A G TMC7 Ensembl:ENSG00000170537 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19009113..19009217 26863196 MeRIP-seq:(Medium) rs771512335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1685590,Human_Splice_Rec_1685618,Human_Splice_Rec_1685648,Human_Splice_Rec_1685666 RMVar_hsa_circ_15050,RMVar_hsa_circ_52662,RMVar_hsa_circ_90422,RMVar_hsa_circ_176880 66141 RMVar_ID_66141 Human_SNP_ID_596665767 m1A Human chr16 - 19067671 19067671 19067671 CCAAAGGCGGGGAGCCGCCGCCGCCCCGGCGCAACTCATTGCCGGAACTAAAAAAAGCAACCACT CCAAAGGCGGGGAGCCGCCGCCGCCCCGGCGCCACTCATTGCCGGAACTAAAAAAAGCAACCACT T G AC099518.4 Ensembl:ENSG00000261465 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:19067626..19067927;chr16:19067627..19067927 26863196 MeRIP-seq:(Medium) rs984134860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1685711 66142 RMVar_ID_66142 Human_SNP_ID_596667631 m1A Human chr16 - 19074000 19074000 19074000 GTGCAAACCCCAGCACGTTCCACAAGGGCATCAGAACTGTTGGCCGGACCCTGAACGTAACCATC GTGCAAACCCCAGCACGTTCCACAAGGGCATCGGAACTGTTGGCCGGACCCTGAACGTAACCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19073951..19074071 26863196 MeRIP-seq:(Medium) rs138490803 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7938,GWAS_ID_7939,GWAS_ID_7940 66143 RMVar_ID_66143 Human_SNP_ID_596668123 m1A Human chr16 + 19075786 19075786 19075786 CCATGGCCTGCACCGTGGCGGTGGAAGAGAGCATAGCACATCACTACAACAACCAGATCAGGACG CCATGGCCTGCACCGTGGCGGTGGAAGAGAGCGTAGCACATCACTACAACAACCAGATCAGGACG A G COQ7 Ensembl:ENSG00000167186 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19075660..19075796 26863196 MeRIP-seq:(Medium) rs1470208185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6497303,Human_RBP_ID_12680849 Human_Splice_Rec_1685720,Human_Splice_Rec_1685721,Human_Splice_Rec_1685728,Human_Splice_Rec_1685729,Human_Splice_Rec_1685738,Human_Splice_Rec_1685739,Human_Splice_Rec_1685750,Human_Splice_Rec_1685758,Human_Splice_Rec_1685759,Human_Splice_Rec_1685768,Human_Splice_Rec_1685769,Human_Splice_Rec_1685778,Human_Splice_Rec_1685784,Human_Splice_Rec_1685785 RMVar_hsa_circ_4737,RMVar_hsa_circ_32297,RMVar_hsa_circ_286922,RMVar_hsa_circ_10800,RMVar_hsa_circ_304525,RMVar_hsa_circ_92355,RMVar_hsa_circ_176895,RMVar_hsa_circ_14224,RMVar_hsa_circ_176896 66144 RMVar_ID_66144 Human_SNP_ID_596671912 m1A Human chr16 - 19089986 19089986 19089986 AGAAGTTGGGTAACACTTGGTAAGTGGTAAGCAAGGATACCTCTCCCATCCCCGCCACTGGTGGT AGAAGTTGGGTAACACTTGGTAAGTGGTAAGCCAGGATACCTCTCCCATCCCCGCCACTGGTGGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19089936..19090060 26863196 MeRIP-seq:(Medium) rs1384560649 Functional Loss SNV dbSNP153 33..33 33 - - - 66145 RMVar_ID_66145 Human_SNP_ID_596678053 m1A Human chr16 + 19114595 19114595 19114595 GGGCGCCCGGGCCGAGCCCGCCGACGGCGTGGATGGCGGCTTCCCGTTGCTTAAGGTGGCCGTCC GGGCGCCCGGGCCGAGCCCGCCGACGGCGTGGGTGGCGGCTTCCCGTTGCTTAAGGTGGCCGTCC A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:19114382..19114840 32194978 MeRIP-seq:(Medium) rs559603064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3004453,Human_miRNA_ID_3010800 RMVar_hsa_circ_82653,RMVar_hsa_circ_176897 66146 RMVar_ID_66146 Human_SNP_ID_596678365 m1A Human chr16 - 19115221 19115221 19115221 GGCCAAGGAGCGCTGCAGATGCGACTGGAACCAGCGCAGCACCAGAGTAGCAGAGAGGTGACGCC GGCCAAGGAGCGCTGCAGATGCGACTGGAACCTGCGCAGCACCAGAGTAGCAGAGAGGTGACGCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:19115132..19115400 26863196 MeRIP-seq:(Medium) rs772939152 Functional Loss SNV dbSNP153 33..33 33 - - - 66147 RMVar_ID_66147 Human_SNP_ID_596678366 m1A Human chr16 - 19115221 19115221 19115221 GGCCAAGGAGCGCTGCAGATGCGACTGGAACCAGCGCAGCACCAGAGTAGCAGAGAGGTGACGCC GGCCAAGGAGCGCTGCAGATGCGACTGGAACCGGCGCAGCACCAGAGTAGCAGAGAGGTGACGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:19115132..19115400 26863196 MeRIP-seq:(Medium) rs772939152 Functional Loss SNV dbSNP153 33..33 33 - - - 66148 RMVar_ID_66148 Human_SNP_ID_596678434 m1A Human chr16 - 19115381 19115381 19115381 CATCTCCCAGATGGACAGCGGGGATGAGACGCACAGCCATAGAAAGGCGGCAGCAGCCGTAGTCA CATCTCCCAGATGGACAGCGGGGATGAGACGCGCAGCCATAGAAAGGCGGCAGCAGCCGTAGTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:19115331..19115432 26863196 MeRIP-seq:(Medium) rs1373576116 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 66149 RMVar_ID_66149 Human_SNP_ID_596679448 m1A Human chr16 + 19119233 19119227 19119234 AGTGAACCAAGAGAAATCCAAAGACCTGGGGAAGGAGGACTTAAGATGAAAGTGAAGCAAGAGAG AGTGAACCAAGAGAAATCCAAAGACCT_______GAGGACTTAAGATGAAAGTGAAGCAAGAGAG TGGGGAAG T ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:19119184..19119313 26863196 MeRIP-seq:(Medium) rs936817145 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_469567,Human_RBP_ID_6497447,Human_RBP_ID_18284491,Human_RBP_ID_23681432 Human_miRNA_ID_2258022,Human_miRNA_ID_2258023 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 66150 RMVar_ID_66150 Human_SNP_ID_596691283 m1A Human chr16 + 19168387 19168387 19168387 CGGTGGGGAGCACGGGACAGCGAGGGAGGCCGAGGCGGGGGCCCTGGGCGCCCGATATCTCCGAA CGGTGGGGAGCACGGGACAGCGAGGGAGGCCGGGGCGGGGGCCCTGGGCGCCCGATATCTCCGAA A G SYT17,AC099518.3 Ensembl:ENSG00000103528,Ensembl:ENSG00000261427 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19168283..19168571 26863196 MeRIP-seq:(Medium) rs1011976657 Functional Loss SNV dbSNP153 33..33 33 - - - 66151 RMVar_ID_66151 Human_SNP_ID_596691291 m1A Human chr16 + 19168409 19168409 19168409 AGGGAGGCCGAGGCGGGGGCCCTGGGCGCCCGATATCTCCGAACCGGGGAGGCGGCCCCGATTCC AGGGAGGCCGAGGCGGGGGCCCTGGGCGCCCGTTATCTCCGAACCGGGGAGGCGGCCCCGATTCC A T SYT17,AC099518.3 Ensembl:ENSG00000103528,Ensembl:ENSG00000261427 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:19168360..19168468 26863196 MeRIP-seq:(Medium) rs1187681156 Functional Loss SNV dbSNP153 33..33 33 - - - 66152 RMVar_ID_66152 Human_SNP_ID_596750434 m1A Human chr16 + 19410802 19410802 19410802 GGAGGTGAGGCGGGTTCGCCAGGAGTGGGGCCAGCGCCCGGGCTGCCAGCCTAGCAGGGGCGTCT GGAGGTGAGGCGGGTTCGCCAGGAGTGGGGCCGGCGCCCGGGCTGCCAGCCTAGCAGGGGCGTCT A G TMC5 Ensembl:ENSG00000103534 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19410732..19411060 26863196 MeRIP-seq:(Medium) rs1030657656 Functional Loss SNV dbSNP153 33..33 33 - - - 66153 RMVar_ID_66153 Human_SNP_ID_596779274 m1A Human chr16 - 19521892 19521892 19521892 TCTCCTTCCTGCTGCTAGTGCTGCTGCTGGTGACGCGGAGCCCGGTCAATGCCTGCCTCCTCACC TCTCCTTCCTGCTGCTAGTGCTGCTGCTGGTGTCGCGGAGCCCGGTCAATGCCTGCCTCCTCACC T A GDE1 Ensembl:ENSG00000006007 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:19521842..19522000 26863196 MeRIP-seq:(Medium) rs757513332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469664,Human_RBP_ID_763247,Human_RBP_ID_1513500,Human_RBP_ID_4392896,Human_RBP_ID_5317455,Human_RBP_ID_5419021,Human_RBP_ID_22800048 66154 RMVar_ID_66154 Human_SNP_ID_596779275 m1A Human chr16 - 19521892 19521892 19521892 TCTCCTTCCTGCTGCTAGTGCTGCTGCTGGTGACGCGGAGCCCGGTCAATGCCTGCCTCCTCACC TCTCCTTCCTGCTGCTAGTGCTGCTGCTGGTGGCGCGGAGCCCGGTCAATGCCTGCCTCCTCACC T C GDE1 Ensembl:ENSG00000006007 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:19521842..19522000 26863196 MeRIP-seq:(Medium) rs757513332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469664,Human_RBP_ID_763247,Human_RBP_ID_1513500,Human_RBP_ID_4392896,Human_RBP_ID_5317455,Human_RBP_ID_5419021,Human_RBP_ID_22800048 66155 RMVar_ID_66155 Human_SNP_ID_596779815 m1A Human chr16 + 19523970 19523967 19523970 CGTTGCAGCCTGAGATCCGTAATATGGCGGGGAGGAGGAGGAGAAGGCGGCGGCGGACCGAGCTG CGTTGCAGCCTGAGATCCGTAATATGGCGG___GGAGGAGGAGAAGGCGGCGGCGGACCGAGCTG GGGA G CCP110 Ensembl:ENSG00000103540 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19523921..19524162 26863196 MeRIP-seq:(Medium) rs921838589 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4354030,Human_RBP_ID_18418678,Human_RBP_ID_23681535 66156 RMVar_ID_66156 Human_SNP_ID_596779816 m1A Human chr16 + 19523970 19523970 19523970 CGTTGCAGCCTGAGATCCGTAATATGGCGGGGAGGAGGAGGAGAAGGCGGCGGCGGACCGAGCTG CGTTGCAGCCTGAGATCCGTAATATGGCGGGGGGGAGGAGGAGAAGGCGGCGGCGGACCGAGCTG A G CCP110 Ensembl:ENSG00000103540 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19523921..19524162 26863196 MeRIP-seq:(Medium) rs199900063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4354030,Human_RBP_ID_18418678,Human_RBP_ID_23681535 66157 RMVar_ID_66157 Human_SNP_ID_596779829 m1A Human chr16 + 19524015 19524015 19524015 GGCGGCGGCGGACCGAGCTGCGCTCTGTCAGTACCATTTGAGCCATTCGCTTCCTGACAAGGCCC GGCGGCGGCGGACCGAGCTGCGCTCTGTCAGTTCCATTTGAGCCATTCGCTTCCTGACAAGGCCC A T CCP110 Ensembl:ENSG00000103540 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:19523920..19524100;chr16:19523912..19524250;chr16:19523909..19524075 26863196 MeRIP-seq:(Medium) rs916823835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4395234,Human_RBP_ID_8805220,Human_RBP_ID_9060604,Human_RBP_ID_9284361,Human_RBP_ID_18418678,Human_RBP_ID_22497298 Human_Splice_Rec_1686295,Human_Splice_Rec_1686323,Human_Splice_Rec_1686351,Human_Splice_Rec_1686353,Human_Splice_Rec_1686359,Human_Splice_Rec_1686363 66158 RMVar_ID_66158 Human_SNP_ID_596780630 m1A Human chr16 + 19527820 19527820 19527820 TCATGCTCTACAAAATCTGCCAAATAATTAAGATCTGTTTTTCCCAGTACATTAAAAATAACATT TCATGCTCTACAAAATCTGCCAAATAATTAAGGTCTGTTTTTCCCAGTACATTAAAAATAACATT A G CCP110 Ensembl:ENSG00000103540 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19527814..19527889 26863196 MeRIP-seq:(Medium) rs1057264944 Functional Loss SNV dbSNP153 33..33 33 - - - 66159 RMVar_ID_66159 Human_SNP_ID_596797542 m1A Human chr16 + 19595041 19595041 19595041 ATTGGGAGCATGCCAGGCTGGCCTGAGAACCAAGGAGGCCAAGAGAGAGGCGATGAGATGAGCCC ATTGGGAGCATGCCAGGCTGGCCTGAGAACCAGGGAGGCCAAGAGAGAGGCGATGAGATGAGCCC A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19595039..19595192 26863196 MeRIP-seq:(Medium) rs1041524196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2184,RMVar_hsa_circ_95731,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176907,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,RMVar_hsa_circ_66758,RMVar_hsa_circ_116602,RMVar_hsa_circ_176909,RMVar_hsa_circ_176910,RMVar_hsa_circ_176911,RMVar_hsa_circ_377326,RMVar_hsa_circ_176912,RMVar_hsa_circ_84469,RMVar_hsa_circ_176913,RMVar_hsa_circ_334585,RMVar_hsa_circ_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_30493,RMVar_hsa_circ_91861,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_176917,RMVar_hsa_circ_293718,RMVar_hsa_circ_176919,RMVar_hsa_circ_176921,RMVar_hsa_circ_26940,RMVar_hsa_circ_176920 66160 RMVar_ID_66160 Human_SNP_ID_596824206 m1A Human chr16 - 19703281 19703277 19703282 TAGACACTGCTGGTTTTGAAGATGGGAAGGGAAGGGTCAGAAGCCAAGGAATGTGTGTGCTGTCT TAGACACTGCTGGTTTTGAAGATGGGAAGGG_____TCAGAAGCCAAGGAATGTGTGTGCTGTCT ACCCTT A KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:19703232..19703461 26863196 MeRIP-seq:(Medium) rs1029103942 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_6497960,Human_RBP_ID_8428932,Human_RBP_ID_12682667 66161 RMVar_ID_66161 Human_SNP_ID_596825099 m1A Human chr16 - 19706598 19706596 19706599 GGGGCAGGGCAGCTCATATTTCGGGAGCCAGGAGAACGAGTGAGTGCTAAAACCTCCTGTTTTCT GGGGCAGGGCAGCTCATATTTCGGGAGCCAG___AACGAGTGAGTGCTAAAACCTCCTGTTTTCT TCTC T KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:19706547..19706646 32194978 MeRIP-seq:(Medium) rs1285492691 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_469760,Human_RBP_ID_6498011,Human_RBP_ID_8805320,Human_RBP_ID_12682762,Human_RBP_ID_22945381,Human_RBP_ID_23681733,Human_RBP_ID_26329854,Human_RBP_ID_26439741 RMVar_hsa_circ_176988,RMVar_hsa_circ_81552,RMVar_hsa_circ_376605,RMVar_hsa_circ_176987,RMVar_hsa_circ_176989 66162 RMVar_ID_66162 Human_SNP_ID_596825363 m1A Human chr16 - 19707205 19707205 19707205 TTTCCTCTCCTCACAGGGAACCCAGTTTGGCCAGTGGGATACTGCTGGTTTTGAGAACGAGGACC TTTCCTCTCCTCACAGGGAACCCAGTTTGGCCGGTGGGATACTGCTGGTTTTGAGAACGAGGACC T C KNOP1 Ensembl:ENSG00000103550 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:19707156..19710450 32194978 MeRIP-seq:(Medium) rs1163678044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888492,Human_RBP_ID_9345608,Human_RBP_ID_19071045,Human_RBP_ID_22541338,Human_RBP_ID_25241374 Human_Splice_Rec_1686898,Human_Splice_Rec_1686904,Human_Splice_Rec_1686908 RMVar_hsa_circ_176988,RMVar_hsa_circ_81552,RMVar_hsa_circ_376605,RMVar_hsa_circ_176987,RMVar_hsa_circ_176989 66163 RMVar_ID_66163 Human_SNP_ID_596826370 m1A Human chr16 - 19710577 19710577 19710577 CTTCTGTCATCCTTCTTGCTCAGGTGAGGCGAAAGGCCTTGCAAGAAGAGATCGATCGCGAGTCA CTTCTGTCATCCTTCTTGCTCAGGTGAGGCGAGAGGCCTTGCAAGAAGAGATCGATCGCGAGTCA T C KNOP1 Ensembl:ENSG00000103550 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19710526..19710623 26863196 MeRIP-seq:(Medium) rs371799105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233554,Human_RBP_ID_889524,Human_RBP_ID_4354285,Human_RBP_ID_9372398,Human_RBP_ID_26328749,Human_RBP_ID_27811675 Human_Splice_Rec_1686896,Human_Splice_Rec_1686897,Human_Splice_Rec_1686902,Human_Splice_Rec_1686903,Human_Splice_Rec_1686906,Human_Splice_Rec_1686907,Human_Splice_Rec_1686914 RMVar_hsa_circ_176988,RMVar_hsa_circ_81552,RMVar_hsa_circ_376605,RMVar_hsa_circ_176987,RMVar_hsa_circ_176989,RMVar_hsa_circ_349422 66164 RMVar_ID_66164 Human_SNP_ID_596827335 m1A Human chr16 - 19714203 19714189 19714204 GAAAAAGATGAAGTCCAAAAAGAAGGTAGAGCAGCCAGTCATCGAGGAGCCAGCTCTGAAAAGGA GAAAAAGATGAAGTCCAAAAAGAAGGTAGAG_______________GAGCCAGCTCTGAAAAGGA CCTCGATGACTGGCTG C KNOP1 Ensembl:ENSG00000103550 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:19714087..19714252 26863196 MeRIP-seq:(Medium) rs1345818266 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_888496,Human_RBP_ID_6498042,Human_RBP_ID_24544493,Human_RBP_ID_26328753,Human_RBP_ID_27810950 Human_Splice_Rec_1686893,Human_Splice_Rec_1686905,Human_Splice_Rec_1686911 66165 RMVar_ID_66165 Human_SNP_ID_596827395 m1A Human chr16 - 19714353 19714353 19714353 AATCCACCAGGAGGGAGATGCCCTCCCAGGCCACTCCAAGCCCTCCAGGTCCATGGAGAGCAGCC AATCCACCAGGAGGGAGATGCCCTCCCAGGCCGCTCCAAGCCCTCCAGGTCCATGGAGAGCAGCC T C KNOP1 Ensembl:ENSG00000103550 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:19714303..19714752 32194978 MeRIP-seq:(Medium) rs1307187334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890424,Human_RBP_ID_9286165,Human_RBP_ID_9372400,Human_RBP_ID_20168913,Human_RBP_ID_26328755,Human_RBP_ID_27810951 66166 RMVar_ID_66166 Human_SNP_ID_596828428 m1A Human chr16 - 19717978 19717978 19717978 AGGCCGCCGCCTCCAGAAAGTTTTCCCGCCTCAGAGCCGGCCCTGGGACCCCACGTAATCCCTCC AGGCCGCCGCCTCCAGAAAGTTTTCCCGCCTCGGAGCCGGCCCTGGGACCCCACGTAATCCCTCC T C KNOP1 Ensembl:ENSG00000103550 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19717974..19718179 26863196 MeRIP-seq:(Medium) rs1048984984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17872827 66167 RMVar_ID_66167 Human_SNP_ID_596828443 m1A Human chr16 - 19718010 19718010 19718010 CCCTCCAGTCGGTGTGCGCCCGCTCCGGCCTGAGGCCGCCGCCTCCAGAAAGTTTTCCCGCCTCA CCCTCCAGTCGGTGTGCGCCCGCTCCGGCCTGCGGCCGCCGCCTCCAGAAAGTTTTCCCGCCTCA T G KNOP1 Ensembl:ENSG00000103550 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:19718008..19718174 26863196 MeRIP-seq:(Medium) rs1331951819 Functional Loss SNV dbSNP153 33..33 33 - - - 66168 RMVar_ID_66168 Human_SNP_ID_597076648 m1A Human chr16 - 20734129 20734129 20734129 GGAAAGATTTTGATTATACAGTTTGTTTTTAAATTGTCTTTTATATTTATTTGTATTTGGTAAGA GGAAAGATTTTGATTATACAGTTTGTTTTTAAGTTGTCTTTTATATTTATTTGTATTTGGTAAGA T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6498358,Human_RBP_ID_24475677,Human_RBP_ID_26939806 Human_miRNA_ID_852851 GWAS_ID_7941,GWAS_ID_7942 RMVar_hsa_circ_79074,RMVar_hsa_circ_177008 66169 RMVar_ID_66169 Human_SNP_ID_597076841 m1A Human chr16 - 20734999 20734999 20734999 TTGGCCTTGAAAATAAAGGGTGCAACTCTCAAATCTTGTTCTAACCCGGCTGGAGGAACCACAAG TTGGCCTTGAAAATAAAGGGTGCAACTCTCAAGTCTTGTTCTAACCCGGCTGGAGGAACCACAAG T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8044864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3492340,Human_RBP_ID_12683620,Human_RBP_ID_17253224,Human_RBP_ID_18284630,Human_RBP_ID_27439842 Human_miRNA_ID_2974498,Human_miRNA_ID_3007691 GWAS_ID_7943,GWAS_ID_7944,GWAS_ID_7945,GWAS_ID_7946 RMVar_hsa_circ_79074,RMVar_hsa_circ_177008 66170 RMVar_ID_66170 Human_SNP_ID_597078723 m1A Human chr16 + 20741707 20741706 20741707 TACTGAGCCTTGCCTTTGCGCTTCCCGCCGCCAGGCTGAGTAGTCTGCTGGGCAGGGGCCGCCAT TACTGAGCCTTGCCTTTGCGCTTCCCGCCGCC_GGCTGAGTAGTCTGCTGGGCAGGGGCCGCCAT CA C ACSM3 Ensembl:ENSG00000005187 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:20741657..20741752 26863196 MeRIP-seq:(Medium) rs1328181211 Functional Loss DEL dbSNP153 33..33 33 - - - 66171 RMVar_ID_66171 Human_SNP_ID_597093098 m1A Human chr16 + 20806376 20806376 20806376 CTGCGGCCAACGCCAGCGCTGGACCCGGAGCTACCCGCCCCCGACCCGGAACTCCCTCGAGTACC CTGCGGCCAACGCCAGCGCTGGACCCGGAGCTCCCCGCCCCCGACCCGGAACTCCCTCGAGTACC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:20806280..20806382 26863410 MeRIP-seq:(Medium) rs1024128716 Functional Loss SNV dbSNP153 33..33 33 - - - 66172 RMVar_ID_66172 Human_SNP_ID_597093099 m1A Human chr16 + 20806376 20806376 20806376 CTGCGGCCAACGCCAGCGCTGGACCCGGAGCTACCCGCCCCCGACCCGGAACTCCCTCGAGTACC CTGCGGCCAACGCCAGCGCTGGACCCGGAGCTTCCCGCCCCCGACCCGGAACTCCCTCGAGTACC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:20806280..20806382 26863410 MeRIP-seq:(Medium) rs1024128716 Functional Loss SNV dbSNP153 33..33 33 - - - 66173 RMVar_ID_66173 Human_SNP_ID_597093116 m1A Human chr16 - 20806405 20806405 20806405 GTCGGGAATGGCGACCAAGCGGCTCGCGCGGTACTCGAGGGAGTTCCGGGTCGGGGGCGGGTAGC GTCGGGAATGGCGACCAAGCGGCTCGCGCGGTCCTCGAGGGAGTTCCGGGTCGGGGGCGGGTAGC T G ERI2 Ensembl:ENSG00000196678 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:20806179..20806435 26863196 MeRIP-seq:(Medium) rs1321429968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393650,Human_RBP_ID_18418681,Human_RBP_ID_19073623 66174 RMVar_ID_66174 Human_SNP_ID_597093129 m1A Human chr16 - 20806421 20806421 20806421 TGGAAAAGCAAGGAGTGTCGGGAATGGCGACCAAGCGGCTCGCGCGGTACTCGAGGGAGTTCCGG TGGAAAAGCAAGGAGTGTCGGGAATGGCGACCGAGCGGCTCGCGCGGTACTCGAGGGAGTTCCGG T C ERI2 Ensembl:ENSG00000196678 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:20806297..20806428 26863196 MeRIP-seq:(Medium) rs886848214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393650,Human_RBP_ID_18418681,Human_RBP_ID_23681976 Human_Splice_Rec_1688297,Human_Splice_Rec_1688323,Human_Splice_Rec_1688357,Human_Splice_Rec_1688373,Human_Splice_Rec_1688387,Human_Splice_Rec_1688405,Human_Splice_Rec_1688415 66175 RMVar_ID_66175 Human_SNP_ID_597114079 m1A Human chr16 - 20900328 20900328 20900328 GCAGATGAAGAGGAGGCGGTGGCAGTGGTGGAAGAAGAGGCGGCGGCGGCGGGGGTAGGGAGCCT GCAGATGAAGAGGAGGCGGTGGCAGTGGTGGAGGAAGAGGCGGCGGCGGCGGGGGTAGGGAGCCT T C DCUN1D3,ERI2 Ensembl:ENSG00000188215,Ensembl:ENSG00000196678 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:20896327..20900721 26863196 MeRIP-seq:(Medium) rs1313461754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418682 66176 RMVar_ID_66176 Human_SNP_ID_597114080 m1A Human chr16 - 20900329 20900329 20900329 CGCAGATGAAGAGGAGGCGGTGGCAGTGGTGGAAGAAGAGGCGGCGGCGGCGGGGGTAGGGAGCC CGCAGATGAAGAGGAGGCGGTGGCAGTGGTGGTAGAAGAGGCGGCGGCGGCGGGGGTAGGGAGCC T A DCUN1D3,ERI2 Ensembl:ENSG00000188215,Ensembl:ENSG00000196678 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:20896295..20900391 26863196 MeRIP-seq:(Medium) rs1457827809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4355132,Human_RBP_ID_18418682 66177 RMVar_ID_66177 Human_SNP_ID_597117634 m1A Human chr16 + 20915523 20915523 20915523 TGGTGCCTCCTGTCAAGTTGCATTTTTATGCAAATTTTCCCTCTTCTATTTTGGTGGGTCTGAAG TGGTGCCTCCTGTCAAGTTGCATTTTTATGCAGATTTTCCCTCTTCTATTTTGGTGGGTCTGAAG A G LYRM1 Ensembl:ENSG00000102897 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:20915518..20915605 26863196 MeRIP-seq:(Medium) rs987609550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6688,RMVar_hsa_circ_96227,RMVar_hsa_circ_112920,RMVar_hsa_circ_177028,RMVar_hsa_circ_177029,RMVar_hsa_circ_272349,RMVar_hsa_circ_177030 66178 RMVar_ID_66178 Human_SNP_ID_597212068 m1A Human chr16 + 21283915 21283915 21283915 CGTTGGGGAGGGTGTTGGGATGAGGAGCCCCAACCAGATGGACGCGCACCCCGCAGCGGCGGAGG CGTTGGGGAGGGTGTTGGGATGAGGAGCCCCAGCCAGATGGACGCGCACCCCGCAGCGGCGGAGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:21283899..21283986 26863410 MeRIP-seq:(Medium) rs926296704 Functional Loss SNV dbSNP153 33..33 33 - - - 66179 RMVar_ID_66179 Human_SNP_ID_597216329 m1A Human chr16 - 21300946 21300946 21300946 CCCAGCCCGCTTCATCTGCGCCCGCTGCCTTTACCCGCCAGCCACTCCGGCGTTTCCACCTCCGT CCCAGCCCGCTTCATCTGCGCCCGCTGCCTTTCCCCGCCAGCCACTCCGGCGTTTCCACCTCCGT T G CRYM Ensembl:ENSG00000103316 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21300864..21301638 26863196 MeRIP-seq:(Medium) rs945965052 Functional Loss SNV dbSNP153 33..33 33 - - - 66180 RMVar_ID_66180 Human_SNP_ID_597216698 m1A Human chr16 + 21301859 21301853 21301859 CCGCCGGGTGGACGCGCGCCCTTCAGCGGCGGAGGCGGAGGCGGCAGCGGCGAGGCCTGAGGGTG CCGCCGGGTGGACGCGCGCCCTTCAGC______GGCGGAGGCGGCAGCGGCGAGGCCTGAGGGTG CGGCGGA C CRYM-AS1 Ensembl:ENSG00000189149 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21301808..21301976 26863196 MeRIP-seq:(Medium) rs767964981 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_3504401,Human_RBP_ID_8184425,Human_RBP_ID_26780255 66181 RMVar_ID_66181 Human_SNP_ID_597216701 m1A Human chr16 + 21301859 21301859 21301859 CCGCCGGGTGGACGCGCGCCCTTCAGCGGCGGAGGCGGAGGCGGCAGCGGCGAGGCCTGAGGGTG CCGCCGGGTGGACGCGCGCCCTTCAGCGGCGGTGGCGGAGGCGGCAGCGGCGAGGCCTGAGGGTG A T CRYM-AS1 Ensembl:ENSG00000189149 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21301808..21301976 26863196 MeRIP-seq:(Medium) rs1393887587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3504401,Human_RBP_ID_8184425,Human_RBP_ID_26780255 66182 RMVar_ID_66182 Human_SNP_ID_597238990 m1A Human chr16 + 21385568 21385567 21385568 TTCTTTTTTTTTTTTTGCCAGATGCCAAATGCAAAAAGGAGCGGAAGAAGAAAAAGCAAGTGACC TTCTTTTTTTTTTTTTGCCAGATGCCAAATGC_AAAAGGAGCGGAAGAAGAAAAAGCAAGTGACC CA C SNX29P1 Ensembl:ENSG00000158482 Pseudogene exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:21385558..21385671 26863196 MeRIP-seq:(Medium) rs1347323970 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1689322 66183 RMVar_ID_66183 Human_SNP_ID_597243402 m1A Human chr16 + 21404896 21404896 21404896 CTGAGGGTAGAGCTGAGGGTGGAAGGGGAGTGAGTAGACACTCGGGAGGTGTCTTGAGATTATCA CTGAGGGTAGAGCTGAGGGTGGAAGGGGAGTGCGTAGACACTCGGGAGGTGTCTTGAGATTATCA A C HSALNG0109939-010,HSALNG0109939-010:2 RNACentral:URS0000EA3783,RNACentral:URS0000EB7E7C lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:21404796..21405002 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 66184 RMVar_ID_66184 Human_SNP_ID_597243405 m1A Human chr16 + 21404901 21404901 21404901 GGTAGAGCTGAGGGTGGAAGGGGAGTGAGTAGACACTCGGGAGGTGTCTTGAGATTATCATCCGC GGTAGAGCTGAGGGTGGAAGGGGAGTGAGTAGGCACTCGGGAGGTGTCTTGAGATTATCATCCGC A G HSALNG0109939-010,HSALNG0109939-010:2 RNACentral:URS0000EA3783,RNACentral:URS0000EB7E7C lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:21404811..21405015 26863196 MeRIP-seq:(Medium) rs1427801545 Functional Loss SNV dbSNP153 33..33 33 - - - 66185 RMVar_ID_66185 Human_SNP_ID_597252613 m1A Human chr16 + 21502196 21502196 21502196 GCCGGGGCCCCCGAGGAGGAGGACGACGAGGAACAGGCGGTGGCGGCAGCTCCTCACGCTCACAC GCCGGGGCCCCCGAGGAGGAGGACGACGAGGAGCAGGCGGTGGCGGCAGCTCCTCACGCTCACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:21501817..21502242;chr16:21502009..21502231 26863196 MeRIP-seq:(Medium) rs1356693157 Functional Loss SNV dbSNP153 33..33 33 - - - 66186 RMVar_ID_66186 Human_SNP_ID_597252622 m1A Human chr16 - 21502204 21502204 21502204 CAGTGGCCGTGTGAGCGTGAGGAGCTGCCGCCACCGCCTGTTCCTCGTCGTCCTCCTCCTCGGGG CAGTGGCCGTGTGAGCGTGAGGAGCTGCCGCCGCCGCCTGTTCCTCGTCGTCCTCCTCCTCGGGG T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:21501976..21502225 26863196 MeRIP-seq:(Medium) rs755471181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762329,Human_RBP_ID_893247,Human_RBP_ID_8188115,Human_RBP_ID_8252832,Human_RBP_ID_8726153,Human_RBP_ID_8812698,Human_RBP_ID_9286553,Human_RBP_ID_9324986,Human_RBP_ID_10483257,Human_RBP_ID_17126046,Human_RBP_ID_17257433,Human_RBP_ID_17371304,Human_RBP_ID_17488542,Human_RBP_ID_18418954,Human_RBP_ID_18482239,Human_RBP_ID_18674701,Human_RBP_ID_20169428,Human_RBP_ID_22370546 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66187 RMVar_ID_66187 Human_SNP_ID_597253327 m1A Human chr16 + 21503251 21503240 21503252 AGGAAGGAAGGAAGGAAACGAGGGAGGGAGGGAAGGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA AGGAAGGAAGGAAGGAAACGAG____________GGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA GGGAGGGAGGGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21503248..21503332 26863196 MeRIP-seq:(Medium) rs1476555042 Functional Loss DEL dbSNP153 23..34 33 - - - 66188 RMVar_ID_66188 Human_SNP_ID_597253328 m1A Human chr16 + 21503251 21503244 21503252 AGGAAGGAAGGAAGGAAACGAGGGAGGGAGGGAAGGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA AGGAAGGAAGGAAGGAAACGAGGGAG________GGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA GGGAGGGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21503248..21503332 26863196 MeRIP-seq:(Medium) rs1167019081 Functional Loss DEL dbSNP153 27..34 33 - - - 66189 RMVar_ID_66189 Human_SNP_ID_597253330 m1A Human chr16 + 21503251 21503248 21503252 AGGAAGGAAGGAAGGAAACGAGGGAGGGAGGGAAGGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA AGGAAGGAAGGAAGGAAACGAGGGAGGGAG____GGAGGGAGGGAGGAAGGAAGGAAAGGAGGGA GGGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21503248..21503332 26863196 MeRIP-seq:(Medium) rs1309102437 Functional Loss DEL dbSNP153 31..34 33 - - - 66190 RMVar_ID_66190 Human_SNP_ID_597255127 m1A Human chr16 - 21507735 21507735 21507735 CAGTGGATAAGGTGGGGGCTGTCTATCAGTGGAGAAGGTGGGGGCTGTCTATCAGTGGAGAAGGT CAGTGGATAAGGTGGGGGCTGTCTATCAGTGGGGAAGGTGGGGGCTGTCTATCAGTGGAGAAGGT T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21507684..21507794 26863196 MeRIP-seq:(Medium) rs1348408891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1527075,Human_RBP_ID_5096498,Human_RBP_ID_6498913,Human_RBP_ID_9067047,Human_RBP_ID_12684887,Human_RBP_ID_22523668 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66191 RMVar_ID_66191 Human_SNP_ID_597255379 m1A Human chr16 - 21508316 21508316 21508316 TCCCCGGAGGCAGAGGCTGCAGCTACTCGGGAAGTAGAGGTGAGAGAATGGCTTGAACTCAGGAG TCCCCGGAGGCAGAGGCTGCAGCTACTCGGGAGGTAGAGGTGAGAGAATGGCTTGAACTCAGGAG T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21508296..21508442 26863196 MeRIP-seq:(Medium) rs554275760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2470163,Human_RBP_ID_3504407,Human_RBP_ID_5183572,Human_RBP_ID_8084831,Human_RBP_ID_8231800,Human_RBP_ID_8812708,Human_RBP_ID_8941726,Human_RBP_ID_12684899,Human_RBP_ID_17188983,Human_RBP_ID_17206538,Human_RBP_ID_17372201,Human_RBP_ID_17669740,Human_RBP_ID_18418955,Human_RBP_ID_18484521,Human_RBP_ID_21959934,Human_RBP_ID_22425549,Human_RBP_ID_24413711 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66192 RMVar_ID_66192 Human_SNP_ID_597255384 m1A Human chr16 - 21508324 21508324 21508324 TCACTTGATCCCCGGAGGCAGAGGCTGCAGCTACTCGGGAAGTAGAGGTGAGAGAATGGCTTGAA TCACTTGATCCCCGGAGGCAGAGGCTGCAGCTGCTCGGGAAGTAGAGGTGAGAGAATGGCTTGAA T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21508319..21508400 26863196 MeRIP-seq:(Medium) rs1290239194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2470163,Human_RBP_ID_3504408,Human_RBP_ID_5183572,Human_RBP_ID_8084831,Human_RBP_ID_8231800,Human_RBP_ID_8941726,Human_RBP_ID_12684899,Human_RBP_ID_17079268,Human_RBP_ID_17188983,Human_RBP_ID_17206538,Human_RBP_ID_17372201,Human_RBP_ID_17565332,Human_RBP_ID_17669740,Human_RBP_ID_18418955,Human_RBP_ID_18482245,Human_RBP_ID_18926643,Human_RBP_ID_21959934,Human_RBP_ID_22425549,Human_RBP_ID_24413711,Human_RBP_ID_26779197 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66193 RMVar_ID_66193 Human_SNP_ID_597259900 m1A Human chr16 + 21519884 21519884 21519884 TGGCTGCCTCCTCGGGCACCGGGCAGGTGGGGAAGAGCGGCTTGAGCAGGTAGGTGGCGAAGACC TGGCTGCCTCCTCGGGCACCGGGCAGGTGGGGGAGAGCGGCTTGAGCAGGTAGGTGGCGAAGACC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:21519876..21519900 26863196 MeRIP-seq:(Medium) rs1479129861 Functional Loss SNV dbSNP153 33..33 33 - - - 66194 RMVar_ID_66194 Human_SNP_ID_597260255 m1A Human chr16 + 21520289 21520289 21520289 GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCATCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCCTCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:21520226..21520450 26863196 MeRIP-seq:(Medium) rs773213854 Functional Loss SNV dbSNP153 33..33 33 - - - 66195 RMVar_ID_66195 Human_SNP_ID_597260256 m1A Human chr16 + 21520289 21520289 21520289 GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCATCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCGTCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:21520226..21520450 26863196 MeRIP-seq:(Medium) rs773213854 Functional Loss SNV dbSNP153 33..33 33 - - - 66196 RMVar_ID_66196 Human_SNP_ID_597260257 m1A Human chr16 + 21520289 21520289 21520289 GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCATCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC GCGCCGCGCCGTCCGCGCGCTTGGCGGCCATCTTCTTCTCCCGCGCCTCTTCCTTCTCCTCGGCC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:21520226..21520450 26863196 MeRIP-seq:(Medium) rs773213854 Functional Loss SNV dbSNP153 33..33 33 - - - 66197 RMVar_ID_66197 Human_SNP_ID_597260261 m1A Human chr16 - 21520292 21520292 21520292 GGTGGCCGAGGAGAAGGAAGAGGCGCGGGAGAAGATGATGGCCGCCAAGCGCGCGGACGGCGCGG GGTGGCCGAGGAGAAGGAAGAGGCGCGGGAGAGGATGATGGCCGCCAAGCGCGCGGACGGCGCGG T C SLC7A5P2,SMG1P3 Ensembl:ENSG00000258186,Ensembl:ENSG00000180747 Pseudogene,Pseudogene exon,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:21520202..21520444 26863196 MeRIP-seq:(Medium) rs1459616986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199722,Human_RBP_ID_762356,Human_RBP_ID_816193,Human_RBP_ID_889531,Human_RBP_ID_1527136,Human_RBP_ID_3947397,Human_RBP_ID_5096511,Human_RBP_ID_5181900,Human_RBP_ID_5524208,Human_RBP_ID_8812569,Human_RBP_ID_9257192,Human_RBP_ID_9841244,Human_RBP_ID_10483175,Human_RBP_ID_12869383,Human_RBP_ID_17189031,Human_RBP_ID_17257451,Human_RBP_ID_17372226,Human_RBP_ID_17488565,Human_RBP_ID_17673271,Human_RBP_ID_17884462,Human_RBP_ID_18544374,Human_RBP_ID_18926547,Human_RBP_ID_18983361,Human_RBP_ID_19077668,Human_RBP_ID_20169337,Human_RBP_ID_21959921,Human_RBP_ID_22944414,Human_RBP_ID_26329881,Human_RBP_ID_27811691 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66198 RMVar_ID_66198 Human_SNP_ID_597260275 m1A Human chr16 - 21520313 21520311 21520314 GCGGCGCGCGCTAGCGGCCCCGGTGGCCGAGGAGAAGGAAGAGGCGCGGGAGAAGATGATGGCCG GCGGCGCGCGCTAGCGGCCCCGGTGGCCGAG___AAGGAAGAGGCGCGGGAGAAGATGATGGCCG TCTC T SLC7A5P2,SMG1P3 Ensembl:ENSG00000258186,Ensembl:ENSG00000180747 Pseudogene,Pseudogene exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:21520251..21520438 26863196 MeRIP-seq:(Medium) rs1201947428 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_893252,Human_RBP_ID_1527136,Human_RBP_ID_3510784,Human_RBP_ID_3948881,Human_RBP_ID_5096511,Human_RBP_ID_5524209,Human_RBP_ID_9841244,Human_RBP_ID_10483175,Human_RBP_ID_12869383,Human_RBP_ID_17669510,Human_RBP_ID_18544374,Human_RBP_ID_18926547,Human_RBP_ID_18983362,Human_RBP_ID_19077668,Human_RBP_ID_21959921,Human_RBP_ID_22944414,Human_RBP_ID_26329881,Human_RBP_ID_27811691 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66199 RMVar_ID_66199 Human_SNP_ID_597260394 m1A Human chr16 - 21520422 21520422 21520422 CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCACAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCTCAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC T A SMG1P3 Ensembl:ENSG00000180747 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:21520376..21520450 26863196 MeRIP-seq:(Medium) rs1243138835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274740,Human_RBP_ID_5524210,Human_RBP_ID_18437254 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66200 RMVar_ID_66200 Human_SNP_ID_597260395 m1A Human chr16 - 21520422 21520422 21520422 CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCACAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCGCAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:21520376..21520450 26863196 MeRIP-seq:(Medium) rs1243138835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274740,Human_RBP_ID_5524210,Human_RBP_ID_18437254 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66201 RMVar_ID_66201 Human_SNP_ID_597260396 m1A Human chr16 - 21520422 21520422 21520422 CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCACAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC CAGCTGCGGGCGGCGGGCGGCGAGCGGCGCGCCCAATCCTCGCTCGGCTGCGGCTCCCGGGTGTC T G SMG1P3 Ensembl:ENSG00000180747 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:21520376..21520450 26863196 MeRIP-seq:(Medium) rs1243138835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274740,Human_RBP_ID_5524210,Human_RBP_ID_18437254 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66202 RMVar_ID_66202 Human_SNP_ID_597274457 m1A Human chr16 + 21558096 21558096 21558096 CGGGCACCACGCTCAGTACGGGGGACAGAGGGAGGAGGCTCTAGGCTCTGACTTGCCCTTGCAGA CGGGCACCACGCTCAGTACGGGGGACAGAGGGCGGAGGCTCTAGGCTCTGACTTGCCCTTGCAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:21558045..21558150 26863196 MeRIP-seq:(Medium) rs1348861916 Functional Loss SNV dbSNP153 33..33 33 - - - 66203 RMVar_ID_66203 Human_SNP_ID_597276814 m1A Human chr16 + 21564574 21564562 21564575 GAGAGAAAGGAAGAGGGGAAGGGAAGGAAGGGAAGGAAGGAAGAGAGAGAGGAAGGAAGGAAGAG GAGAGAAAGGAAGAGGGGAAG_____________GGAAGGAAGAGAGAGAGGAAGGAAGGAAGAG GGGAAGGAAGGGAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:21564557..21564662 26863196 MeRIP-seq:(Medium) rs1481572409 Functional Loss DEL dbSNP153 22..34 33 - - - 66204 RMVar_ID_66204 Human_SNP_ID_597287372 m1A Human chr16 - 21599777 21599777 21599777 TCCGCAGCGTCCACATCCTCCGCGCCAGCCACACGGACGCCAGGCTCAGGCACAGCCAGCCCGCC TCCGCAGCGTCCACATCCTCCGCGCCAGCCACCCGGACGCCAGGCTCAGGCACAGCCAGCCCGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:21599726..21599875 32194978 MeRIP-seq:(Medium) rs1489522004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 66205 RMVar_ID_66205 Human_SNP_ID_597290330 m1A Human chr16 + 21612588 21612588 21612588 TAGTCTTCTGGTTTTTTGTTTTTGGATTTCTTAGGTGACACTTCGGTTGTGTGTTTTAATTTTTG TAGTCTTCTGGTTTTTTGTTTTTGGATTTCTTCGGTGACACTTCGGTTGTGTGTTTTAATTTTTG A C METTL9 Ensembl:ENSG00000197006 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:21612587..21612675 26863196 MeRIP-seq:(Medium) rs1443031222 Functional Loss SNV dbSNP153 33..33 33 - - - 66206 RMVar_ID_66206 Human_SNP_ID_597301099 m1A Human chr16 + 21655489 21655489 21655489 AGTCCGCACCCTCCGGGATGTGCCCTTGGAAGAGGGTCTGTGTTCACAATTACGTGAAGGGAGGA AGTCCGCACCCTCCGGGATGTGCCCTTGGAAGGGGGTCTGTGTTCACAATTACGTGAAGGGAGGA A G METTL9 Ensembl:ENSG00000197006 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:21655227..21655677 32194978 MeRIP-seq:(Medium) rs958797262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470230,Human_RBP_ID_17253283,Human_RBP_ID_17371308,Human_RBP_ID_17488219,Human_RBP_ID_17873136,Human_RBP_ID_27238424,Human_RBP_ID_27439932,Human_RBP_ID_27559910,Human_RBP_ID_27657189 RMVar_hsa_circ_97560,RMVar_hsa_circ_103488,RMVar_hsa_circ_177080,RMVar_hsa_circ_105458,RMVar_hsa_circ_177087,RMVar_hsa_circ_81036,RMVar_hsa_circ_177089,RMVar_hsa_circ_177090 66207 RMVar_ID_66207 Human_SNP_ID_597301243 m1A Human chr16 + 21656185 21656185 21656185 TCAGATACAGAACTTCAGGGACCCCTCCCCCCACCCCCCCAGTTAATGCTGCTGTGAAAAATGCA TCAGATACAGAACTTCAGGGACCCCTCCCCCCCCCCCCCCAGTTAATGCTGCTGTGAAAAATGCA A C METTL9 Ensembl:ENSG00000197006 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:21656175..21656276 32194978 MeRIP-seq:(Medium) rs879107780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1418584,Human_miRNA_ID_1702590,Human_miRNA_ID_1938053,Human_miRNA_ID_1938054,Human_miRNA_ID_1949153,Human_miRNA_ID_1949154,Human_miRNA_ID_2101568,Human_miRNA_ID_2101569,Human_miRNA_ID_2107523,Human_miRNA_ID_2107524,Human_miRNA_ID_2740172,Human_miRNA_ID_2740173,Human_miRNA_ID_3040762,Human_miRNA_ID_3040763 RMVar_hsa_circ_97560,RMVar_hsa_circ_103488,RMVar_hsa_circ_177080,RMVar_hsa_circ_105458,RMVar_hsa_circ_177087,RMVar_hsa_circ_81036,RMVar_hsa_circ_177089,RMVar_hsa_circ_177090 66208 RMVar_ID_66208 Human_SNP_ID_597363903 m1A Human chr16 + 21953414 21953414 21953414 CTTTAATCCGGCAGTGACCGTGTGTCAGAACAATCTTGAATCATGAAGCTACTAACCAGAGCCGG CTTTAATCCGGCAGTGACCGTGTGTCAGAACAGTCTTGAATCATGAAGCTACTAACCAGAGCCGG A G UQCRC2 Ensembl:ENSG00000140740 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21953351..21957325 26863196 MeRIP-seq:(Medium) rs776820013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1514015,Human_RBP_ID_1839300,Human_RBP_ID_3947399,Human_RBP_ID_4393663,Human_RBP_ID_5316610,Human_RBP_ID_9324994,Human_RBP_ID_12686136,Human_RBP_ID_17255941,Human_RBP_ID_17371311,Human_RBP_ID_18437259,Human_RBP_ID_22440881,Human_RBP_ID_26940116 Human_Splice_Rec_1690311,Human_Splice_Rec_1690319,Human_Splice_Rec_1690333,Human_Splice_Rec_1690359,Human_Splice_Rec_1690361,Human_Splice_Rec_1690385,Human_Splice_Rec_1690395,Human_Splice_Rec_1690417 Human_miRNA_ID_1273382,Human_miRNA_ID_2618013 RMVar_hsa_circ_111801,RMVar_hsa_circ_177106 66209 RMVar_ID_66209 Human_SNP_ID_597363904 m1A Human chr16 + 21953414 21953414 21953414 CTTTAATCCGGCAGTGACCGTGTGTCAGAACAATCTTGAATCATGAAGCTACTAACCAGAGCCGG CTTTAATCCGGCAGTGACCGTGTGTCAGAACATTCTTGAATCATGAAGCTACTAACCAGAGCCGG A T UQCRC2 Ensembl:ENSG00000140740 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:21953351..21957325 26863196 MeRIP-seq:(Medium) rs776820013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1514015,Human_RBP_ID_1839300,Human_RBP_ID_3947399,Human_RBP_ID_4393663,Human_RBP_ID_5316610,Human_RBP_ID_9324994,Human_RBP_ID_12686136,Human_RBP_ID_17255941,Human_RBP_ID_17371311,Human_RBP_ID_18437259,Human_RBP_ID_22440881,Human_RBP_ID_26940116 Human_Splice_Rec_1690311,Human_Splice_Rec_1690319,Human_Splice_Rec_1690333,Human_Splice_Rec_1690359,Human_Splice_Rec_1690361,Human_Splice_Rec_1690385,Human_Splice_Rec_1690395,Human_Splice_Rec_1690417 Human_miRNA_ID_1273382,Human_miRNA_ID_2618013 RMVar_hsa_circ_111801,RMVar_hsa_circ_177106 66210 RMVar_ID_66210 Human_SNP_ID_597364856 m1A Human chr16 + 21957264 21957264 21957264 TAGAGATTTTATTCCCTCAAAGTTGCCCCCAAAGTTAAAGCCACAGCTGCGCCTGCAGGAGCACC TAGAGATTTTATTCCCTCAAAGTTGCCCCCAACGTTAAAGCCACAGCTGCGCCTGCAGGAGCACC A C UQCRC2 Ensembl:ENSG00000140740 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:21957226..21957300 26863196 MeRIP-seq:(Medium) rs1373834770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895027,Human_RBP_ID_4355611,Human_RBP_ID_17255942,Human_RBP_ID_17371313,Human_RBP_ID_23682336 Human_Splice_Rec_1690312,Human_Splice_Rec_1690313,Human_Splice_Rec_1690320,Human_Splice_Rec_1690321,Human_Splice_Rec_1690334,Human_Splice_Rec_1690335,Human_Splice_Rec_1690362,Human_Splice_Rec_1690363,Human_Splice_Rec_1690396,Human_Splice_Rec_1690397,Human_Splice_Rec_1690418,Human_Splice_Rec_1690419 RMVar_hsa_circ_3962,RMVar_hsa_circ_111801,RMVar_hsa_circ_326545,RMVar_hsa_circ_338917,RMVar_hsa_circ_177106,RMVar_hsa_circ_371720,RMVar_hsa_circ_330331,RMVar_hsa_circ_123497,RMVar_hsa_circ_282894,RMVar_hsa_circ_101405,RMVar_hsa_circ_177107,RMVar_hsa_circ_177109,RMVar_hsa_circ_177111,RMVar_hsa_circ_3817,RMVar_hsa_circ_177110,RMVar_hsa_circ_177108 66211 RMVar_ID_66211 Human_SNP_ID_597364948 m1A Human chr16 - 21957481 21957481 21957481 CATATCTACTGCCTGCTTTAATGAACAAACCAATTCTTGATACAGGAGAATAGTTTTCCAAAGAA CATATCTACTGCCTGCTTTAATGAACAAACCATTTCTTGATACAGGAGAATAGTTTTCCAAAGAA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:21953404..21958597 32194978 MeRIP-seq:(Medium) rs1302174997 Functional Loss SNV dbSNP153 33..33 33 - - - 66212 RMVar_ID_66212 Human_SNP_ID_597364949 m1A Human chr16 - 21957481 21957481 21957481 CATATCTACTGCCTGCTTTAATGAACAAACCAATTCTTGATACAGGAGAATAGTTTTCCAAAGAA CATATCTACTGCCTGCTTTAATGAACAAACCAGTTCTTGATACAGGAGAATAGTTTTCCAAAGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:21953404..21958597 32194978 MeRIP-seq:(Medium) rs1302174997 Functional Loss SNV dbSNP153 33..33 33 - - - 66213 RMVar_ID_66213 Human_SNP_ID_597368476 m1A Human chr16 + 21972063 21972063 21972063 TCCTCGGTGCTGGGCCACATGTCAAGAGGGGCAGCAACACCACCAGCCATCTGCACCAGGCTGTT TCCTCGGTGCTGGGCCACATGTCAAGAGGGGCGGCAACACCACCAGCCATCTGCACCAGGCTGTT A G UQCRC2 Ensembl:ENSG00000140740 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:21968668..21976220 32194978 MeRIP-seq:(Medium) rs768119386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470292,Human_RBP_ID_761394,Human_RBP_ID_817868,Human_RBP_ID_890430,Human_RBP_ID_3948890,Human_RBP_ID_18983377,Human_RBP_ID_22440887 Human_Splice_Rec_1690351,Human_Splice_Rec_1690379,Human_Splice_Rec_1690413,Human_Splice_Rec_1690445,Human_Splice_Rec_1690453 Human_miRNA_ID_271921,Human_miRNA_ID_2052245,Human_miRNA_ID_2151902,Human_miRNA_ID_2420368 RMVar_hsa_circ_3962,RMVar_hsa_circ_111801,RMVar_hsa_circ_177106,RMVar_hsa_circ_371720,RMVar_hsa_circ_123497,RMVar_hsa_circ_177113,RMVar_hsa_circ_177111,RMVar_hsa_circ_3817,RMVar_hsa_circ_177110,RMVar_hsa_circ_96903,RMVar_hsa_circ_112829,RMVar_hsa_circ_91547,RMVar_hsa_circ_177114,RMVar_hsa_circ_80409,RMVar_hsa_circ_88966,RMVar_hsa_circ_177112,RMVar_hsa_circ_177117,RMVar_hsa_circ_105330,RMVar_hsa_circ_177118,RMVar_hsa_circ_126670,RMVar_hsa_circ_295599,RMVar_hsa_circ_177119,RMVar_hsa_circ_301338,RMVar_hsa_circ_270153,RMVar_hsa_circ_177121,RMVar_hsa_circ_177123,RMVar_hsa_circ_177122,RMVar_hsa_circ_96562,RMVar_hsa_circ_375160,RMVar_hsa_circ_177120,RMVar_hsa_circ_325961,RMVar_hsa_circ_86931,RMVar_hsa_circ_177131,RMVar_hsa_circ_54235,RMVar_hsa_circ_177125,RMVar_hsa_circ_177127,RMVar_hsa_circ_177128,RMVar_hsa_circ_177126,RMVar_hsa_circ_320162,RMVar_hsa_circ_177130,RMVar_hsa_circ_338247,RMVar_hsa_circ_375797,RMVar_hsa_circ_272380,RMVar_hsa_circ_177133,RMVar_hsa_circ_177132,RMVar_hsa_circ_76007,RMVar_hsa_circ_85445,RMVar_hsa_circ_177136,RMVar_hsa_circ_122964,RMVar_hsa_circ_290329,RMVar_hsa_circ_177135,RMVar_hsa_circ_80420,RMVar_hsa_circ_177138,RMVar_hsa_circ_30269,RMVar_hsa_circ_177139,RMVar_hsa_circ_177137 66214 RMVar_ID_66214 Human_SNP_ID_597370371 m1A Human chr16 + 21980606 21980606 21980606 GTCAGTGGAGTCTTCTGAGTGTTTCCTGGAAGAAGTCGGGTCCCAGGCTCTAGTTGCTGGTTCTT GTCAGTGGAGTCTTCTGAGTGTTTCCTGGAAGTAGTCGGGTCCCAGGCTCTAGTTGCTGGTTCTT A T UQCRC2 Ensembl:ENSG00000140740 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs190027776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470296,Human_RBP_ID_895046,Human_RBP_ID_1839371,Human_RBP_ID_6499482,Human_RBP_ID_8443858,Human_RBP_ID_9060864,Human_RBP_ID_17255960,Human_RBP_ID_17371320,Human_RBP_ID_17652601,Human_RBP_ID_22053034,Human_RBP_ID_22440889 Human_Splice_Rec_1690356,Human_Splice_Rec_1690357,Human_Splice_Rec_1690414,Human_Splice_Rec_1690415,Human_Splice_Rec_1690455 RMVar_hsa_circ_3962,RMVar_hsa_circ_111801,RMVar_hsa_circ_177106,RMVar_hsa_circ_123497,RMVar_hsa_circ_177111,RMVar_hsa_circ_112829,RMVar_hsa_circ_80409,RMVar_hsa_circ_177112,RMVar_hsa_circ_295599,RMVar_hsa_circ_96562,RMVar_hsa_circ_177120,RMVar_hsa_circ_86931,RMVar_hsa_circ_24334,RMVar_hsa_circ_177131,RMVar_hsa_circ_177127,RMVar_hsa_circ_177128,RMVar_hsa_circ_375797,RMVar_hsa_circ_85445,RMVar_hsa_circ_177136,RMVar_hsa_circ_122964,RMVar_hsa_circ_113642,RMVar_hsa_circ_177139,RMVar_hsa_circ_80136,RMVar_hsa_circ_177140,RMVar_hsa_circ_177141,RMVar_hsa_circ_115974,RMVar_hsa_circ_177143 66215 RMVar_ID_66215 Human_SNP_ID_597376886 m1A Human chr16 + 22008497 22008497 22008497 GGGAGACCCGGACTGAGGAGAGGACGGGGTGGAGGGTCCCGGCCGGAGGCTAGCCTGAGGAGACC GGGAGACCCGGACTGAGGAGAGGACGGGGTGGCGGGTCCCGGCCGGAGGCTAGCCTGAGGAGACC A C MOSMO Ensembl:ENSG00000185716 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22008449..22008661 26863196 MeRIP-seq:(Medium) rs1274761472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3504415,Human_RBP_ID_5359809,Human_RBP_ID_8184434,Human_RBP_ID_9420529,Human_RBP_ID_26780263 66216 RMVar_ID_66216 Human_SNP_ID_597419389 m1A Human chr16 - 22195725 22195725 22195725 AGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACACCTCAGAAGGTCTCAC AGGCTCCAGTCATTTCGATGGCGTGGGTTCGATTCCCACCGCTGCCACACCTCAGAAGGTCTCAC T A tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22195681..22195765 26863196 MeRIP-seq:(Medium) rs921470323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269744,Human_RBP_ID_277311,Human_RBP_ID_470365,Human_RBP_ID_1003412,Human_RBP_ID_1177312,Human_RBP_ID_1281298,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_2470564,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5274765,Human_RBP_ID_5419054,Human_RBP_ID_5440235,Human_RBP_ID_5464787,Human_RBP_ID_5495261,Human_RBP_ID_6499986,Human_RBP_ID_8251997,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9286591,Human_RBP_ID_9842114,Human_RBP_ID_12688447,Human_RBP_ID_17253321,Human_RBP_ID_17369012,Human_RBP_ID_17485449,Human_RBP_ID_17689826,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178808,Human_RBP_ID_18199987,Human_RBP_ID_18512948,Human_RBP_ID_18529668,Human_RBP_ID_18674881,Human_RBP_ID_20102940,Human_RBP_ID_22048930,Human_RBP_ID_22198161,Human_RBP_ID_22800228,Human_RBP_ID_22945424,Human_RBP_ID_23127966,Human_RBP_ID_23163312,Human_RBP_ID_23682595,Human_RBP_ID_24412972,Human_RBP_ID_24477477,Human_RBP_ID_25242696,Human_RBP_ID_26446640,Human_RBP_ID_26748952,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439974,Human_RBP_ID_27657284 66217 RMVar_ID_66217 Human_SNP_ID_597419390 m1A Human chr16 - 22195725 22195725 22195725 AGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACACCTCAGAAGGTCTCAC AGGCTCCAGTCATTTCGATGGCGTGGGTTCGAGTCCCACCGCTGCCACACCTCAGAAGGTCTCAC T C tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22195681..22195765 26863196 MeRIP-seq:(Medium) rs921470323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269744,Human_RBP_ID_277311,Human_RBP_ID_470365,Human_RBP_ID_1003412,Human_RBP_ID_1177312,Human_RBP_ID_1281298,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_2470564,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5274765,Human_RBP_ID_5419054,Human_RBP_ID_5440235,Human_RBP_ID_5464787,Human_RBP_ID_5495261,Human_RBP_ID_6499986,Human_RBP_ID_8251997,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9286591,Human_RBP_ID_9842114,Human_RBP_ID_12688447,Human_RBP_ID_17253321,Human_RBP_ID_17369012,Human_RBP_ID_17485449,Human_RBP_ID_17689826,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178808,Human_RBP_ID_18199987,Human_RBP_ID_18512948,Human_RBP_ID_18529668,Human_RBP_ID_18674881,Human_RBP_ID_20102940,Human_RBP_ID_22048930,Human_RBP_ID_22198161,Human_RBP_ID_22800228,Human_RBP_ID_22945424,Human_RBP_ID_23127966,Human_RBP_ID_23163312,Human_RBP_ID_23682595,Human_RBP_ID_24412972,Human_RBP_ID_24477477,Human_RBP_ID_25242696,Human_RBP_ID_26446640,Human_RBP_ID_26748952,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439974,Human_RBP_ID_27657284 66218 RMVar_ID_66218 Human_SNP_ID_597419391 m1A Human chr16 - 22195726 22195726 22195726 TAGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACACCTCAGAAGGTCTCA TAGGCTCCAGTCATTTCGATGGCGTGGGTTCGCATCCCACCGCTGCCACACCTCAGAAGGTCTCA T G tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1288217953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269744,Human_RBP_ID_277311,Human_RBP_ID_470365,Human_RBP_ID_1003412,Human_RBP_ID_1177312,Human_RBP_ID_1281298,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_2470564,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5274765,Human_RBP_ID_5419054,Human_RBP_ID_5440235,Human_RBP_ID_5464787,Human_RBP_ID_5495261,Human_RBP_ID_6499986,Human_RBP_ID_8251997,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9286591,Human_RBP_ID_9842114,Human_RBP_ID_12688447,Human_RBP_ID_17253321,Human_RBP_ID_17369012,Human_RBP_ID_17485449,Human_RBP_ID_17689826,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178808,Human_RBP_ID_18199987,Human_RBP_ID_18437270,Human_RBP_ID_18512948,Human_RBP_ID_18529668,Human_RBP_ID_18674881,Human_RBP_ID_20102940,Human_RBP_ID_22048930,Human_RBP_ID_22198161,Human_RBP_ID_22800228,Human_RBP_ID_22945424,Human_RBP_ID_23127966,Human_RBP_ID_23163312,Human_RBP_ID_23682595,Human_RBP_ID_24412972,Human_RBP_ID_24477477,Human_RBP_ID_25241957,Human_RBP_ID_26446513,Human_RBP_ID_26748952,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439974,Human_RBP_ID_27657284 66219 RMVar_ID_66219 Human_SNP_ID_597419408 m1A Human chr16 + 22195739 22195739 22195739 GGTGTGGCAGCGGTGGGATTCGAACCCACGCCATCGAAATGACTGGAGCCTAAATCCAGCGCCTT GGTGTGGCAGCGGTGGGATTCGAACCCACGCCGTCGAAATGACTGGAGCCTAAATCCAGCGCCTT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr16:22195646..22195820;chr16:22195653..22195782 26863196 MeRIP-seq:(Medium) rs1479166212 Functional Loss SNV dbSNP153 33..33 33 - - - 66220 RMVar_ID_66220 Human_SNP_ID_597419409 m1A Human chr16 - 22195740 22195740 22195740 TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACAC TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGGTGGCGTGGGTTCGAATCCCACCGCTGCCACAC T C tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:22195710..22195784 26863196 MeRIP-seq:(Medium) rs1484017196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277312,Human_RBP_ID_470365,Human_RBP_ID_1003413,Human_RBP_ID_1131254,Human_RBP_ID_1177312,Human_RBP_ID_1281299,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5097606,Human_RBP_ID_5259115,Human_RBP_ID_5274748,Human_RBP_ID_5289863,Human_RBP_ID_5440236,Human_RBP_ID_5464788,Human_RBP_ID_5495261,Human_RBP_ID_5536097,Human_RBP_ID_6499986,Human_RBP_ID_8251998,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9284451,Human_RBP_ID_12688447,Human_RBP_ID_17253322,Human_RBP_ID_17369013,Human_RBP_ID_17485450,Human_RBP_ID_17582529,Human_RBP_ID_17587143,Human_RBP_ID_17689828,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178525,Human_RBP_ID_18199848,Human_RBP_ID_18207363,Human_RBP_ID_18437270,Human_RBP_ID_18529669,Human_RBP_ID_18674881,Human_RBP_ID_20102941,Human_RBP_ID_21926765,Human_RBP_ID_22497372,Human_RBP_ID_22802929,Human_RBP_ID_22936658,Human_RBP_ID_23110392,Human_RBP_ID_23111459,Human_RBP_ID_23127966,Human_RBP_ID_23682595,Human_RBP_ID_24477477,Human_RBP_ID_24538744,Human_RBP_ID_25197064,Human_RBP_ID_26446513,Human_RBP_ID_26748903,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439975,Human_RBP_ID_27657285 66221 RMVar_ID_66221 Human_SNP_ID_597419410 m1A Human chr16 - 22195740 22195740 22195740 TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACAC TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGCTGGCGTGGGTTCGAATCCCACCGCTGCCACAC T G tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:22195710..22195784 26863196 MeRIP-seq:(Medium) rs1484017196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277312,Human_RBP_ID_470365,Human_RBP_ID_1003413,Human_RBP_ID_1131254,Human_RBP_ID_1177312,Human_RBP_ID_1281299,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5097606,Human_RBP_ID_5259115,Human_RBP_ID_5274748,Human_RBP_ID_5289863,Human_RBP_ID_5440236,Human_RBP_ID_5464788,Human_RBP_ID_5495261,Human_RBP_ID_5536097,Human_RBP_ID_6499986,Human_RBP_ID_8251998,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9284451,Human_RBP_ID_12688447,Human_RBP_ID_17253322,Human_RBP_ID_17369013,Human_RBP_ID_17485450,Human_RBP_ID_17582529,Human_RBP_ID_17587143,Human_RBP_ID_17689828,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178525,Human_RBP_ID_18199848,Human_RBP_ID_18207363,Human_RBP_ID_18437270,Human_RBP_ID_18529669,Human_RBP_ID_18674881,Human_RBP_ID_20102941,Human_RBP_ID_21926765,Human_RBP_ID_22497372,Human_RBP_ID_22802929,Human_RBP_ID_22936658,Human_RBP_ID_23110392,Human_RBP_ID_23111459,Human_RBP_ID_23127966,Human_RBP_ID_23682595,Human_RBP_ID_24477477,Human_RBP_ID_24538744,Human_RBP_ID_25197064,Human_RBP_ID_26446513,Human_RBP_ID_26748903,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439975,Human_RBP_ID_27657285 66222 RMVar_ID_66222 Human_SNP_ID_597432577 m1A Human chr16 - 22248627 22248627 22248627 CCTCAGAACCAACCCACTCTCCACCTTGGCCCATAGCCCAGCCAACCTCCTGGGTTGGGTTGGAG CCTCAGAACCAACCCACTCTCCACCTTGGCCCCTAGCCCAGCCAACCTCCTGGGTTGGGTTGGAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22248589..22248702 26863196 MeRIP-seq:(Medium) rs1380576849 Functional Loss SNV dbSNP153 33..33 33 - - - 66223 RMVar_ID_66223 Human_SNP_ID_597437773 m1A Human chr16 + 22267715 22267715 22267715 TCAGGTAGAAGGAACAGCATGTGCTTAGGCCCAGAGGTGAGAGACAAGGTGCACCCGTGTAGCTA TCAGGTAGAAGGAACAGCATGTGCTTAGGCCCCGAGGTGAGAGACAAGGTGCACCCGTGTAGCTA A C EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:22267666..22267839 26863196 MeRIP-seq:(Medium) rs1164317542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12688682 RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_94459,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177169,RMVar_hsa_circ_311928,RMVar_hsa_circ_177173 66224 RMVar_ID_66224 Human_SNP_ID_597442141 m1A Human chr16 + 22285539 22285539 22285539 TTTCATTTGATGTTTCAAATAGCAAAGATGCTAGGTGCGGTGGCTCCCGCCTGTAATCTCAGCAC TTTCATTTGATGTTTCAAATAGCAAAGATGCTGGGTGCGGTGGCTCCCGCCTGTAATCTCAGCAC A G EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs961968176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445877 RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 66225 RMVar_ID_66225 Human_SNP_ID_597446968 m1A Human chr16 + 22302985 22302985 22302985 CTGGCTCTCCTCTAGTATGGCCAATGAAGAGGATGACCCAGTTGTACAGGAGGTAACTGCTGCTC CTGGCTCTCCTCTAGTATGGCCAATGAAGAGGGTGACCCAGTTGTACAGGAGGTAACTGCTGCTC A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:22302913..22303048 26863196 MeRIP-seq:(Medium) rs375024210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891679,Human_RBP_ID_1514129,Human_RBP_ID_1839475,Human_RBP_ID_3947418,Human_RBP_ID_4394474,Human_RBP_ID_9372430,Human_RBP_ID_18983386 Human_Splice_Rec_1690882,Human_Splice_Rec_1690883,Human_Splice_Rec_1690922,Human_Splice_Rec_1690923,Human_Splice_Rec_1690974,Human_Splice_Rec_1690975,Human_Splice_Rec_1691014,Human_Splice_Rec_1691015,Human_Splice_Rec_1691024,Human_Splice_Rec_1691025,Human_Splice_Rec_1691062,Human_Splice_Rec_1691063,Human_Splice_Rec_1691082,Human_Splice_Rec_1691083,Human_Splice_Rec_1691115,Human_Splice_Rec_1691121,Human_Splice_Rec_1691125,Human_Splice_Rec_1691163 Human_miRNA_ID_2717604 RMVar_hsa_circ_17319,RMVar_hsa_circ_110883,RMVar_hsa_circ_112539,RMVar_hsa_circ_177176,RMVar_hsa_circ_177177,RMVar_hsa_circ_278193,RMVar_hsa_circ_349584,RMVar_hsa_circ_80178,RMVar_hsa_circ_177178,RMVar_hsa_circ_177179 66226 RMVar_ID_66226 Human_SNP_ID_597453230 m1A Human chr16 + 22325932 22325932 22325932 GATCAAGGAGGAGCCCGTGAGCGAGGAGGGCGAGGAGGACGAGGAGCAGGAGGCGGAGGAGGAGC GATCAAGGAGGAGCCCGTGAGCGAGGAGGGCGTGGAGGACGAGGAGCAGGAGGCGGAGGAGGAGC A T POLR3E Ensembl:ENSG00000058600 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:22325763..22326087 26863196 MeRIP-seq:(Medium) rs747177864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18985704,Human_RBP_ID_22583937,Human_RBP_ID_22944418,Human_RBP_ID_26328775 RMVar_hsa_circ_16996,RMVar_hsa_circ_82200,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_107474,RMVar_hsa_circ_177189,RMVar_hsa_circ_65469,RMVar_hsa_circ_127810,RMVar_hsa_circ_177192,RMVar_hsa_circ_93989,RMVar_hsa_circ_19681,RMVar_hsa_circ_177193 66227 RMVar_ID_66227 Human_SNP_ID_597453232 m1A Human chr16 + 22325935 22325935 22325935 CAAGGAGGAGCCCGTGAGCGAGGAGGGCGAGGAGGACGAGGAGCAGGAGGCGGAGGAGGAGCCCA CAAGGAGGAGCCCGTGAGCGAGGAGGGCGAGGCGGACGAGGAGCAGGAGGCGGAGGAGGAGCCCA A C POLR3E Ensembl:ENSG00000058600 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22325801..22325975 26863196 MeRIP-seq:(Medium) rs1465458774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18985704,Human_RBP_ID_22583937,Human_RBP_ID_22944418,Human_RBP_ID_26328775 RMVar_hsa_circ_16996,RMVar_hsa_circ_82200,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_107474,RMVar_hsa_circ_177189,RMVar_hsa_circ_65469,RMVar_hsa_circ_127810,RMVar_hsa_circ_177192,RMVar_hsa_circ_93989,RMVar_hsa_circ_19681,RMVar_hsa_circ_177193 66228 RMVar_ID_66228 Human_SNP_ID_597455640 m1A Human chr16 - 22333763 22333763 22333763 GCTCTGTGTCGTCTGAAGCAAGTCGAGGCCCTACTTCTGGTTCCGCCCTTCTTCCTTGGGCTTAG GCTCTGTGTCGTCTGAAGCAAGTCGAGGCCCTGCTTCTGGTTCCGCCCTTCTTCCTTGGGCTTAG T C AC092338.3 Ensembl:ENSG00000286808 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:22333713..22333895 26863196 MeRIP-seq:(Medium) rs566958920 Functional Loss SNV dbSNP153 33..33 33 - - - 66229 RMVar_ID_66229 Human_SNP_ID_597459256 m1A Human chr16 - 22347598 22347598 22347598 GAGCAGCAGCTGGGGGCCACAGGTGCCTACCGAGCACGGGCGCTGGAACTAGAGGCCGAGGTGGC GAGCAGCAGCTGGGGGCCACAGGTGCCTACCGTGCACGGGCGCTGGAACTAGAGGCCGAGGTGGC T A CDR2 Ensembl:ENSG00000140743 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22347548..22347735 26863196 MeRIP-seq:(Medium) rs752229403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9372439,Human_RBP_ID_18411669,Human_RBP_ID_22054929,Human_RBP_ID_26329899 Human_miRNA_ID_2590234 RMVar_hsa_circ_92225,RMVar_hsa_circ_177195,RMVar_hsa_circ_76129,RMVar_hsa_circ_177194 66230 RMVar_ID_66230 Human_SNP_ID_597459733 m1A Human chr16 - 22349362 22349362 22349362 AGCCAAGTGGAGGAGCTGAAGTCATCTGGCCAAGGGAGAAGGAGCCCGGGAAAGTGTGACCAGGA AGCCAAGTGGAGGAGCTGAAGTCATCTGGCCAGGGGAGAAGGAGCCCGGGAAAGTGTGACCAGGA T C CDR2 Ensembl:ENSG00000140743 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:22349315..22374391 32194978 MeRIP-seq:(Medium) rs1323754538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4356145,Human_RBP_ID_9372441,Human_RBP_ID_18983406,Human_RBP_ID_26328095,Human_RBP_ID_26811102 Human_Splice_Rec_1691224,Human_Splice_Rec_1691225,Human_Splice_Rec_1691236,Human_Splice_Rec_1691237,Human_Splice_Rec_1691242,Human_Splice_Rec_1691243,Human_Splice_Rec_1691248,Human_Splice_Rec_1691249,Human_Splice_Rec_1691252,Human_Splice_Rec_1691260 Human_miRNA_ID_2218348 RMVar_hsa_circ_39305,RMVar_hsa_circ_92225,RMVar_hsa_circ_177195,RMVar_hsa_circ_76129,RMVar_hsa_circ_177194,RMVar_hsa_circ_278794,RMVar_hsa_circ_177196 66231 RMVar_ID_66231 Human_SNP_ID_597459874 m1A Human chr16 - 22349823 22349823 22349823 TTACAGTATCTGACGAAGCAAGTGGAACTTCTACGGCAGATGAACGAACAACATGCAAAGGTTTA TTACAGTATCTGACGAAGCAAGTGGAACTTCTGCGGCAGATGAACGAACAACATGCAAAGGTTTA T C CDR2 Ensembl:ENSG00000140743 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:22349772..22374291 32194978 MeRIP-seq:(Medium) rs1426021841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9372444,Human_RBP_ID_19073693,Human_RBP_ID_23682773 Human_Splice_Rec_1691222,Human_Splice_Rec_1691234,Human_Splice_Rec_1691240,Human_Splice_Rec_1691246,Human_Splice_Rec_1691258 RMVar_hsa_circ_39305,RMVar_hsa_circ_92225,RMVar_hsa_circ_177195,RMVar_hsa_circ_278794,RMVar_hsa_circ_94969,RMVar_hsa_circ_177196,RMVar_hsa_circ_177197 66232 RMVar_ID_66232 Human_SNP_ID_597465999 m1A Human chr16 - 22374462 22374462 22374462 AGGCAGCCGGCCGGTCGGCGGCCGCCGGCGGGAACGGGGCTGAGGCGGCGCAGCGGAGTCTGGGC AGGCAGCCGGCCGGTCGGCGGCCGCCGGCGGGCACGGGGCTGAGGCGGCGCAGCGGAGTCTGGGC T G CDR2 Ensembl:ENSG00000140743 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:22374340..22374541 26863410 MeRIP-seq:(Medium) rs904993354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394476 66233 RMVar_ID_66233 Human_SNP_ID_597471192 m1A Human chr16 - 22396120 22396102 22396120 AGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAAAAGGAAAGAAAGAAAGAAGAAAGAAAGAAAGAA AGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAA__________________GAAAGAAAGAAAGAA CTTCTTTCTTTCTTTCCTT C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:22396081..22396218 26863196 MeRIP-seq:(Medium) rs1479404932 Functional Loss DEL dbSNP153 33..50 33 - - - 66234 RMVar_ID_66234 Human_SNP_ID_597471223 m1A Human chr16 - 22396120 22396118 22396120 AGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAAAAGGAAAGAAAGAAAGAAGAAAGAAAGAAAGAA AGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAA__GGAAAGAAAGAAAGAAGAAAGAAAGAAAGAA CTT C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:22396081..22396218 26863196 MeRIP-seq:(Medium) rs1491140232 Functional Loss DEL dbSNP153 33..34 33 - - - 66235 RMVar_ID_66235 Human_SNP_ID_597471241 m1A Human chr16 - 22396147 22396145 22396147 AGAGAGAGAGAGAAAGAAAAGAAAGAAAGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAAAAGGAA AGAGAGAGAGAGAAAGAAAAGAAAGAAAGAAA__GAAAGAAAAGGTAAGAAAGAAAGAAAAGGAA CCT C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22396133..22396239 26863196 MeRIP-seq:(Medium) rs200761358 Functional Loss DEL dbSNP153 33..34 33 - - - 66236 RMVar_ID_66236 Human_SNP_ID_597471243 m1A Human chr16 - 22396147 22396146 22396147 AGAGAGAGAGAGAAAGAAAAGAAAGAAAGAAAAGGAAAGAAAAGGTAAGAAAGAAAGAAAAGGAA AGAGAGAGAGAGAAAGAAAAGAAAGAAAGAAA_GGAAAGAAAAGGTAAGAAAGAAAGAAAAGGAA CT C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:22396133..22396239 26863196 MeRIP-seq:(Medium) rs1401791048 Functional Loss DEL dbSNP153 33..33 33 - - - 66237 RMVar_ID_66237 Human_SNP_ID_597478143 m1A Human chr16 - 22424865 22424860 22424865 GAAGGAGGGGCAGTGCCCATAAGACGAAGGGAAGGGAGCGGACAAGGTGCAGAGAACTGCACACA GAAGGAGGGGCAGTGCCCATAAGACGAAGGGA_____GCGGACAAGGTGCAGAGAACTGCACACA CTCCCT C CDR2,RRN3P3 Ensembl:ENSG00000140743,Ensembl:ENSG00000257122 Protein coding,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:22424817..22424910 26863196 MeRIP-seq:(Medium) rs1309397728 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3510775,Human_RBP_ID_5648128,Human_RBP_ID_9841474,Human_RBP_ID_10483348,Human_RBP_ID_17189109,Human_RBP_ID_17206713,Human_RBP_ID_18926638 66238 RMVar_ID_66238 Human_SNP_ID_597655120 m1A Human chr16 + 23149287 23149287 23149287 CCGTTACCTTGGACATGGCGGCGGCCGCAGACACTCATCACCGCGCCCGCCCGCCCGGCCCGCGG CCGTTACCTTGGACATGGCGGCGGCCGCAGACCCTCATCACCGCGCCCGCCCGCCCGGCCCGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23149260..23149384 26863196 MeRIP-seq:(Medium) rs1382721088 Functional Loss SNV dbSNP153 33..33 33 - - - 66239 RMVar_ID_66239 Human_SNP_ID_597698743 m1A Human chr16 - 23316167 23316167 23316167 TGATGATGGGGATGATGGTGGTGATGATGATGATGGTGGTGATGGTGATGATGGTGATGGTGGTG TGATGATGGGGATGATGGTGGTGATGATGATGGTGGTGGTGATGGTGATGATGGTGATGGTGGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:23316117..23316200 26863196 MeRIP-seq:(Medium) rs1353035237 Functional Loss SNV dbSNP153 33..33 33 - - - 66240 RMVar_ID_66240 Human_SNP_ID_597698756 m1A Human chr16 - 23316188 23316188 23316188 TGATGGTGAGGATGGTGATGGTGATGATGGGGATGATGGTGGTGATGATGATGATGGTGGTGATG TGATGGTGAGGATGGTGATGGTGATGATGGGGGTGATGGTGGTGATGATGATGATGGTGGTGATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:23316125..23316202 26863196 MeRIP-seq:(Medium) rs1405847178 Functional Loss SNV dbSNP153 33..33 33 - - - 66241 RMVar_ID_66241 Human_SNP_ID_597718267 m1A Human chr16 + 23389423 23389423 23389423 ATCCAAACTCACACAAACTCGCACACACACTCACATGTACACACACTCACATGCACACACTCTCA ATCCAAACTCACACAAACTCGCACACACACTCCCATGTACACACACTCACATGCACACACTCTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:23389391..23389473 26863196 MeRIP-seq:(Medium) rs982531986 Functional Loss SNV dbSNP153 33..33 33 - - - 66242 RMVar_ID_66242 Human_SNP_ID_597741226 m1A Human chr16 - 23479406 23479404 23479406 TGGTTGTGAGTAGGAGAGTGAGCTGGACCCTCAGGGAGCACATGCCTGCTGCTGAGGGAATCGGG TGGTTGTGAGTAGGAGAGTGAGCTGGACCCTC__GGAGCACATGCCTGCTGCTGAGGGAATCGGG CCT C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:23479355..23479504 26863196 MeRIP-seq:(Medium) rs1274486984 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5356554,Human_RBP_ID_12693266 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_37605,RMVar_hsa_circ_283563,RMVar_hsa_circ_177295 66243 RMVar_ID_66243 Human_SNP_ID_597741227 m1A Human chr16 - 23479406 23479406 23479406 TGGTTGTGAGTAGGAGAGTGAGCTGGACCCTCAGGGAGCACATGCCTGCTGCTGAGGGAATCGGG TGGTTGTGAGTAGGAGAGTGAGCTGGACCCTCTGGGAGCACATGCCTGCTGCTGAGGGAATCGGG T A GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:23479355..23479504 26863196 MeRIP-seq:(Medium) rs1468502904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5356554,Human_RBP_ID_12693266 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_37605,RMVar_hsa_circ_283563,RMVar_hsa_circ_177295 66244 RMVar_ID_66244 Human_SNP_ID_597741245 m1A Human chr16 + 23479480 23479480 23479480 CCTCAGCAGCAGGTATGTGCTCCCTCAGCAGCAGACACGTGTTCTCCGAGGGTCCAGCTCACTCC CCTCAGCAGCAGGTATGTGCTCCCTCAGCAGCGGACACGTGTTCTCCGAGGGTCCAGCTCACTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:23479431..23479571 26863196 MeRIP-seq:(Medium) rs1210839190 Functional Loss SNV dbSNP153 33..33 33 - - - 66245 RMVar_ID_66245 Human_SNP_ID_597748941 m1A Human chr16 - 23508469 23508469 23508469 AGGAGAAGAGAGAACTTTGAATTTGGTAACCAACCAGTTATTTAATGAGACATCCTTGAGTTAAA AGGAGAAGAGAGAACTTTGAATTTGGTAACCAGCCAGTTATTTAATGAGACATCCTTGAGTTAAA T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:23508467..23509094 26863196 MeRIP-seq:(Medium) rs942874623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12694316,Human_RBP_ID_22936899 66246 RMVar_ID_66246 Human_SNP_ID_597749549 m1A Human chr16 + 23510323 23510323 23510323 GCTGCGCCGAAGGCCTGCCAGGCTACTCACTGAGCCACAGCTCCAGCGACGCTGCCGGGCCCGGG GCTGCGCCGAAGGCCTGCCAGGCTACTCACTGGGCCACAGCTCCAGCGACGCTGCCGGGCCCGGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:23510301..23510476 26863196 MeRIP-seq:(Medium) rs974675998 Functional Loss SNV dbSNP153 33..33 33 - - - 66247 RMVar_ID_66247 Human_SNP_ID_597749644 m1A Human chr16 - 23510429 23510429 23510429 GCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGAGCGATGGCGGCGACCGCG GCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCGGCGTCGGGGCTGGAGCGATGGCGGCGACCGCG T C GGA2 Ensembl:ENSG00000103365 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:23510274..23510500 26863196 MeRIP-seq:(Medium) rs2285522 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_234750,Human_RBP_ID_4392912,Human_RBP_ID_9374038,Human_RBP_ID_18418961,Human_RBP_ID_18985748 66248 RMVar_ID_66248 Human_SNP_ID_597749665 m1A Human chr16 - 23510447 23510447 23510447 GAGCGCCAGGACGCTACAGCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGA GAGCGCCAGGACGCTACAGCGGCTGAAGAGGCGGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGA T C GGA2 Ensembl:ENSG00000103365 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:23510323..23510478;chr16:23510326..23510475 26863196 MeRIP-seq:(Medium) rs978183015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234750,Human_RBP_ID_4392912,Human_RBP_ID_9374038,Human_RBP_ID_18418961 66249 RMVar_ID_66249 Human_SNP_ID_597752948 m1A Human chr16 + 23522859 23522859 23522859 AAGCGAGATCAGCTAGGATTGCGGTCATGTGAATGCTTGGCTGGAATTGAAGGACCAGCTTTCAA AAGCGAGATCAGCTAGGATTGCGGTCATGTGAGTGCTTGGCTGGAATTGAAGGACCAGCTTTCAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:23522760..23522861 32194978 MeRIP-seq:(Medium) rs1420516019 Functional Loss SNV dbSNP153 33..33 33 - - - 66250 RMVar_ID_66250 Human_SNP_ID_597762892 m1A Human chr16 + 23558081 23558081 23558081 CGGCGGCCGAGGACTCCGGCGCCGCACGAGGCAGCCTGCAGCCGGCCCCGGCCCAGCCCCCTGGG CGGCGGCCGAGGACTCCGGCGCCGCACGAGGCGGCCTGCAGCCGGCCCCGGCCCAGCCCCCTGGG A G UBFD1 Ensembl:ENSG00000103353 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:23557991..23558082 26863410 MeRIP-seq:(Medium) rs1256282926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816917,Human_RBP_ID_5359899 RMVar_hsa_circ_99560,RMVar_hsa_circ_177321 66251 RMVar_ID_66251 Human_SNP_ID_597762932 m1A Human chr16 + 23558142 23558142 23558142 TGGGGACCCCGCAGCCCAGGCCTCGGTCAGCAACGGCGAAGACGCGGGCGGCGGCGCGGGCAGGG TGGGGACCCCGCAGCCCAGGCCTCGGTCAGCAGCGGCGAAGACGCGGGCGGCGGCGCGGGCAGGG A G UBFD1 Ensembl:ENSG00000103353 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23557909..23558231 26863196 MeRIP-seq:(Medium) rs1197688635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761024,Human_RBP_ID_4357177,Human_RBP_ID_27811712 RMVar_hsa_circ_99560,RMVar_hsa_circ_177321 66252 RMVar_ID_66252 Human_SNP_ID_597763488 m1A Human chr16 - 23559678 23559678 23559678 TTTCTCAAGACCAAGAAGCACAAGATGGACTCACTTTCTGCCTGCAGAGAGGCTCCTTCTTGTTC TTTCTCAAGACCAAGAAGCACAAGATGGACTCGCTTTCTGCCTGCAGAGAGGCTCCTTCTTGTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23559643..23559724 26863196 MeRIP-seq:(Medium) rs765661347 Functional Loss SNV dbSNP153 33..33 33 - - - 66253 RMVar_ID_66253 Human_SNP_ID_597766579 m1A Human chr16 + 23570949 23570947 23570949 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTT__AAAAAAAAAAAAGCAGTTTCAATTGAAATATT TTA T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1491190198 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 66254 RMVar_ID_66254 Human_SNP_ID_597766590 m1A Human chr16 + 23570949 23570949 23570949 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTTAAAAAAAAAAAAGCAGTTTCAATTGAAATATT A T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs77282410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 66255 RMVar_ID_66255 Human_SNP_ID_597766591 m1A Human chr16 + 23570949 23570949 23570951 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTTTTAAAAAAAAAAGCAGTTTCAATTGAAATATT AAA TTT UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs796242080 Functional Loss MNV dbSNP153 33..35 33 - - - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 66256 RMVar_ID_66256 Human_SNP_ID_597767193 m1A Human chr16 - 23573193 23573193 23573193 CTTCCTTTATCCACCTGCACGGCCCCTGCCACAGTGAGGGAAAGATCTGGTCCCTCTGACAGTAA CTTCCTTTATCCACCTGCACGGCCCCTGCCACGGTGAGGGAAAGATCTGGTCCCTCTGACAGTAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:23573043..23573193 32194978 MeRIP-seq:(Medium) rs1388238957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177325 66257 RMVar_ID_66257 Human_SNP_ID_597767373 m1A Human chr16 + 23573838 23573837 23573839 CAGCCTTTCTTTGCCAGGGGCAGAGAAGGGAAAGGGGGTAGATTGAGTGTGCCAAGGGCCGTGCA CAGCCTTTCTTTGCCAGGGGCAGAGAAGGGAA__GGGGTAGATTGAGTGTGCCAAGGGCCGTGCA AAG A UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:23573442..23573841 32194978 MeRIP-seq:(Medium) rs1050327959 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4357273,Human_RBP_ID_6501694,Human_RBP_ID_8186921,Human_RBP_ID_17123893,Human_RBP_ID_17255981,Human_RBP_ID_17873705,Human_RBP_ID_23128007,Human_RBP_ID_23228728 RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 66258 RMVar_ID_66258 Human_SNP_ID_597767385 m1A Human chr16 + 23573876 23573876 23573876 TAGATTGAGTGTGCCAAGGGCCGTGCAAGGGCAGGCTTGCTTTCCACCCATCTGCTGAGGGAGCC TAGATTGAGTGTGCCAAGGGCCGTGCAAGGGCGGGCTTGCTTTCCACCCATCTGCTGAGGGAGCC A G UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:23573826..23573900 32194978 MeRIP-seq:(Medium) rs993924789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470879,Human_RBP_ID_761049,Human_RBP_ID_818555,Human_RBP_ID_5236568,Human_RBP_ID_8186921,Human_RBP_ID_17122505,Human_RBP_ID_17253455,Human_RBP_ID_17485649,Human_RBP_ID_17873705,Human_RBP_ID_20093532,Human_RBP_ID_23229391,Human_RBP_ID_24475787,Human_RBP_ID_26445907 RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 66259 RMVar_ID_66259 Human_SNP_ID_597772493 m1A Human chr16 - 23591549 23591549 23591549 CCCAGGTGGCGGAGAAGGAACAGAGGTCTGTAAGCAGGAGTTTTGGAGACAGGTCAGGAGTTCAT CCCAGGTGGCGGAGAAGGAACAGAGGTCTGTAGGCAGGAGTTTTGGAGACAGGTCAGGAGTTCAT T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:23591545..23591735 26863196 MeRIP-seq:(Medium) rs1164444283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6501766,Human_RBP_ID_12695660,Human_RBP_ID_23274499 RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 66260 RMVar_ID_66260 Human_SNP_ID_597794049 m1A Human chr16 + 23669522 23669522 23669522 CCTCAAGTCATCATTGTGGCCAGGAAGATGGAATACACCAAATGGACAGGCCTGGCATGTACCCA CCTCAAGTCATCATTGTGGCCAGGAAGATGGACTACACCAAATGGACAGGCCTGGCATGTACCCA A C DCTN5 Ensembl:ENSG00000166847 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23669473..23669577 26863196 MeRIP-seq:(Medium) rs1358103830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1003538,Human_RBP_ID_6501973,Human_RBP_ID_8805762,Human_RBP_ID_9374050,Human_RBP_ID_17369180,Human_RBP_ID_17873791,Human_RBP_ID_18190422,Human_RBP_ID_18675456,Human_RBP_ID_20105228,Human_RBP_ID_22054942,Human_RBP_ID_22198556,Human_RBP_ID_26440142,Human_RBP_ID_26811109,Human_RBP_ID_26940678,Human_RBP_ID_27238959 66261 RMVar_ID_66261 Human_SNP_ID_597796266 m1A Human chr16 + 23678921 23678921 23678921 GGAGGCTCTGCTCGGATCGAGGTCTGCAGCGCAGCTTCGGGAGCATGAGTGCTGCAGTGACTGCA GGAGGCTCTGCTCGGATCGAGGTCTGCAGCGCCGCTTCGGGAGCATGAGTGCTGCAGTGACTGCA A C PLK1 Ensembl:ENSG00000166851 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:23678851..23679221;chr16:23678851..23679056 26863196 MeRIP-seq:(Medium) rs768369206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234506,Human_RBP_ID_1514752,Human_RBP_ID_1839910,Human_RBP_ID_4357668,Human_RBP_ID_6502048,Human_RBP_ID_8805823,Human_RBP_ID_17873841,Human_RBP_ID_18419457,Human_RBP_ID_18675473,Human_RBP_ID_22053054,Human_RBP_ID_22441848,Human_RBP_ID_26940710 66262 RMVar_ID_66262 Human_SNP_ID_597796321 m1A Human chr16 - 23679034 23679034 23679034 ACTAGGACCTCCGGGATCTCTTTCGCCGGTGGAGCCGCCGCCGGAGCTCCGGGAGCTGCAACTCC ACTAGGACCTCCGGGATCTCTTTCGCCGGTGGGGCCGCCGCCGGAGCTCCGGGAGCTGCAACTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23678851..23679085 26863196 MeRIP-seq:(Medium) rs1358684596 Functional Loss SNV dbSNP153 33..33 33 - - - 66263 RMVar_ID_66263 Human_SNP_ID_597799058 m1A Human chr16 - 23689348 23689348 23689348 GGAGTTGGGATGGGAACTCACGGTGAGGTAGGACTCAGTGCCGTCACGCTCTATGTACTGCAGGC GGAGTTGGGATGGGAACTCACGGTGAGGTAGGTCTCAGTGCCGTCACGCTCTATGTACTGCAGGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:23689298..23689398 26863196 MeRIP-seq:(Medium) rs893016241 Functional Loss SNV dbSNP153 33..33 33 - - - 66264 RMVar_ID_66264 Human_SNP_ID_597799279 m1A Human chr16 + 23689971 23689971 23689971 GCCTGAGTCTCCTGGAGGAGTACGGCTGCTGCAAGGAGCTGGCCAGCCGGCTCCGCTACGCCCGC GCCTGAGTCTCCTGGAGGAGTACGGCTGCTGCGAGGAGCTGGCCAGCCGGCTCCGCTACGCCCGC A G PLK1 Ensembl:ENSG00000166851 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:23689920..23690268 32194978 MeRIP-seq:(Medium) rs1271355789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761760,Human_RBP_ID_1281396,Human_RBP_ID_4357764,Human_RBP_ID_8805849,Human_RBP_ID_17371334,Human_RBP_ID_18675507,Human_RBP_ID_22441856 RMVar_hsa_circ_94720,RMVar_hsa_circ_100779,RMVar_hsa_circ_117169,RMVar_hsa_circ_177353,RMVar_hsa_circ_177354,RMVar_hsa_circ_177355,RMVar_hsa_circ_99883,RMVar_hsa_circ_96131,RMVar_hsa_circ_177356,RMVar_hsa_circ_105557,RMVar_hsa_circ_177357,RMVar_hsa_circ_177358 66265 RMVar_ID_66265 Human_SNP_ID_598025630 m1A Human chr16 + 24569475 24569475 24569475 AGAAGGAGAGTGAAAACGCTCCAGGAGATGGTAAAGGAAATAAGCATAAGAAACACAGAAAAAGA AGAAGGAGAGTGAAAACGCTCCAGGAGATGGTGAAGGAAATAAGCATAAGAAACACAGAAAAAGA A G RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24569424..24569542 26863196 MeRIP-seq:(Medium) rs138617858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46143,Human_RBP_ID_2471371,Human_RBP_ID_22583997 66266 RMVar_ID_66266 Human_SNP_ID_598025817 m1A Human chr16 + 24570046 24570046 24570046 AAAAGTGAAGAAGGACTATTCCAAAGATGTCAAATCAGAAAAGCTAACAACTAAGGAAGAAAAGG AAAAGTGAAGAAGGACTATTCCAAAGATGTCACATCAGAAAAGCTAACAACTAAGGAAGAAAAGG A C RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24569996..24570099 26863196 MeRIP-seq:(Medium) rs764128496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46146,Human_RBP_ID_2471382,Human_RBP_ID_26329915 66267 RMVar_ID_66267 Human_SNP_ID_598025818 m1A Human chr16 + 24570046 24570046 24570046 AAAAGTGAAGAAGGACTATTCCAAAGATGTCAAATCAGAAAAGCTAACAACTAAGGAAGAAAAGG AAAAGTGAAGAAGGACTATTCCAAAGATGTCAGATCAGAAAAGCTAACAACTAAGGAAGAAAAGG A G RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24569996..24570099 26863196 MeRIP-seq:(Medium) rs764128496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46146,Human_RBP_ID_2471382,Human_RBP_ID_26329915 66268 RMVar_ID_66268 Human_SNP_ID_598025819 m1A Human chr16 + 24570046 24570046 24570046 AAAAGTGAAGAAGGACTATTCCAAAGATGTCAAATCAGAAAAGCTAACAACTAAGGAAGAAAAGG AAAAGTGAAGAAGGACTATTCCAAAGATGTCATATCAGAAAAGCTAACAACTAAGGAAGAAAAGG A T RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24569996..24570099 26863196 MeRIP-seq:(Medium) rs764128496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46146,Human_RBP_ID_2471382,Human_RBP_ID_26329915 66269 RMVar_ID_66269 Human_SNP_ID_598026603 m1A Human chr16 + 24572292 24572292 24572292 AAGAAGGAAAAGAAAAAACACAAGAAACATAAAAAGCATAAGAAGCATAAGAAACATGCAGGCAC AAGAAGGAAAAGAAAAAACACAAGAAACATAAGAAGCATAAGAAGCATAAGAAACATGCAGGCAC A G RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24572242..24572368 26863196 MeRIP-seq:(Medium) rs770610761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1526959,Human_RBP_ID_9444025,Human_RBP_ID_24544397 66270 RMVar_ID_66270 Human_SNP_ID_598068379 m1A Human chr16 - 24729684 24729666 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG__________________GCCCCAGACCGGAAG CCTGCGGCGGCGGCGGTGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1239610295 Functional Loss DEL dbSNP153 33..50 33 - - - 66271 RMVar_ID_66271 Human_SNP_ID_598068397 m1A Human chr16 - 24729684 24729669 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG_______________CAGGCCCCAGACCGGAAG GCGGCGGCGGCGGTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1166358176 Functional Loss DEL dbSNP153 33..47 33 - - - 66272 RMVar_ID_66272 Human_SNP_ID_598068402 m1A Human chr16 - 24729684 24729672 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG____________CCGCAGGCCCCAGACCGGAAG GCGGCGGCGGTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1221579955 Functional Loss DEL dbSNP153 33..44 33 - - - 66273 RMVar_ID_66273 Human_SNP_ID_598068407 m1A Human chr16 - 24729684 24729675 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG_________CCGCCGCAGGCCCCAGACCGGAAG GCGGCGGTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1232029763 Functional Loss DEL dbSNP153 33..41 33 - - - 66274 RMVar_ID_66274 Human_SNP_ID_598068411 m1A Human chr16 - 24729684 24729678 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG______CCGCCGCCGCAGGCCCCAGACCGGAAG GCGGTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs766064851 Functional Loss DEL dbSNP153 33..38 33 - - - 66275 RMVar_ID_66275 Human_SNP_ID_598068417 m1A Human chr16 - 24729684 24729681 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCG___CCGCCGCCGCCGCAGGCCCCAGACCGGAAG GTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1204843845 Functional Loss DEL dbSNP153 33..35 33 - - - 66276 RMVar_ID_66276 Human_SNP_ID_598068425 m1A Human chr16 - 24729684 24729682 24729685 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC___ACCGCCGCCGCCGCAGGCCCCAGACCGGAAG TGTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1425015987 Functional Loss DEL dbSNP153 32..34 33 - - - 66277 RMVar_ID_66277 Human_SNP_ID_598068428 m1A Human chr16 - 24729684 24729684 24729684 CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGACACCGCCGCCGCCGCAGGCCCCAGACCGGAAG CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGGCCCCAGACCGGAAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:24729580..24729858 26863196 MeRIP-seq:(Medium) rs1483155786 Functional Loss SNV dbSNP153 33..33 33 - - - 66278 RMVar_ID_66278 Human_SNP_ID_598068481 m1A Human chr16 + 24729719 24729692 24729719 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GCGGCG___________________________GCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GGCGGCGGCGGCGGCGGCGGCGGCGGCA G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:24729606..24729836 26863196 MeRIP-seq:(Medium) rs1480036149 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_4397584,Human_RBP_ID_8430316 66279 RMVar_ID_66279 Human_SNP_ID_598068512 m1A Human chr16 + 24729719 24729707 24729719 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GCGGCGGCGGCGGCGGCGGCG____________GCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GGCGGCGGCGGCA G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:24729606..24729836 26863196 MeRIP-seq:(Medium) rs1431565753 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4397584,Human_RBP_ID_8430316 66280 RMVar_ID_66280 Human_SNP_ID_598068523 m1A Human chr16 + 24729719 24729713 24729719 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GCGGCGGCGGCGGCGGCGGCGGCGGCG______GCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GGCGGCA G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:24729606..24729836 26863196 MeRIP-seq:(Medium) rs990932723 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4397584,Human_RBP_ID_8430316 66281 RMVar_ID_66281 Human_SNP_ID_598068531 m1A Human chr16 + 24729719 24729716 24729719 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCG___GCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GGCA G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:24729606..24729836 26863196 MeRIP-seq:(Medium) rs1308246681 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4397584,Human_RBP_ID_8430316 66282 RMVar_ID_66282 Human_SNP_ID_598068534 m1A Human chr16 + 24729719 24729719 24729719 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGTCGGTGTAGAAAATGGCGCTGGTGCAG A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:24729606..24729836 26863196 MeRIP-seq:(Medium) rs866998467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4397584,Human_RBP_ID_8430316 66283 RMVar_ID_66283 Human_SNP_ID_598068545 m1A Human chr16 - 24729744 24729744 24729744 GCGCCGCGGGGAGAGGCCCGAGCCGCTGCACCAGCGCCATTTTCTACACCGACCCGCTGCCGCCG GCGCCGCGGGGAGAGGCCCGAGCCGCTGCACCGGCGCCATTTTCTACACCGACCCGCTGCCGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24729696..24729955 26863196 MeRIP-seq:(Medium) rs1490368739 Functional Loss SNV dbSNP153 33..33 33 - - - 66284 RMVar_ID_66284 Human_SNP_ID_598073864 m1A Human chr16 + 24750774 24750771 24750774 GAAGAACAGTTGATGGAAGAAAAGAAAAAGAAAAAAGACGACAAGAAAAAGAAGGAAGCTGCTCA GAAGAACAGTTGATGGAAGAAAAGAAAAAG___AAAGACGACAAGAAAAAGAAGGAAGCTGCTCA GAAA G TNRC6A Ensembl:ENSG00000090905 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24750695..24750844 26863196 MeRIP-seq:(Medium) rs748404766 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_891745,Human_RBP_ID_1526919,Human_RBP_ID_1840124,Human_RBP_ID_6502952,Human_RBP_ID_22654006,Human_RBP_ID_24544503 Human_Splice_Rec_1693106,Human_Splice_Rec_1693110,Human_Splice_Rec_1693111,Human_Splice_Rec_1693158,Human_Splice_Rec_1693159 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_334738,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_177404 66285 RMVar_ID_66285 Human_SNP_ID_598075826 m1A Human chr16 - 24759471 24759471 24759471 TCTGCTCACAATGCCTTTCTTCTCTTAGCTCTACCTTTCAAATCCCTACCTGTCTTCCAACCAAT TCTGCTCACAATGCCTTTCTTCTCTTAGCTCTGCCTTTCAAATCCCTACCTGTCTTCCAACCAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24759464..24759551 26863196 MeRIP-seq:(Medium) rs894276047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177408 66286 RMVar_ID_66286 Human_SNP_ID_598075872 m1A Human chr16 + 24759674 24759674 24759674 TGGAATGTCATGGTCATAAGCTGTGGAAATTTAACTTTGCCAGTAGTGCCTAAAGTCACCAATAG TGGAATGTCATGGTCATAAGCTGTGGAAATTTGACTTTGCCAGTAGTGCCTAAAGTCACCAATAG A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24759669..24759827 26863196 MeRIP-seq:(Medium) rs1457997160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12699446 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_339498 66287 RMVar_ID_66287 Human_SNP_ID_598080236 m1A Human chr16 + 24777068 24777053 24777068 AGCCAACAATCAGCAGCCACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC AGCCAACAATCAGCAGCC_______________ACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC CACAGCAGCAGCAGCA C TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:24776880..24777162 26863196 MeRIP-seq:(Medium) rs756416479 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_895599,Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 66288 RMVar_ID_66288 Human_SNP_ID_598080248 m1A Human chr16 + 24777068 24777057 24777069 AGCCAACAATCAGCAGCCACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC AGCCAACAATCAGCAGCCACAG____________CAGCAGCAGCCGCAGCAGCAGCAGCCACAGC GCAGCAGCAGCAA G TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:24776880..24777162 26863196 MeRIP-seq:(Medium) rs780413327 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_895599,Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 66289 RMVar_ID_66289 Human_SNP_ID_598080253 m1A Human chr16 + 24777068 24777060 24777069 AGCCAACAATCAGCAGCCACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC AGCCAACAATCAGCAGCCACAGCAG_________CAGCAGCAGCCGCAGCAGCAGCAGCCACAGC GCAGCAGCAA G TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:24776880..24777162 26863196 MeRIP-seq:(Medium) rs775973571 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_895599,Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 66290 RMVar_ID_66290 Human_SNP_ID_598080259 m1A Human chr16 + 24777068 24777068 24777068 AGCCAACAATCAGCAGCCACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC AGCCAACAATCAGCAGCCACAGCAGCAGCAGCCACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC A C TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:24776880..24777162 26863196 MeRIP-seq:(Medium) rs4788428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895599,Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 66291 RMVar_ID_66291 Human_SNP_ID_598080289 m1A Human chr16 + 24777086 24777086 24777086 ACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGCAGCAGCCACAGCCGCAGC ACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCCGCAGCAGCCACAGCAGCAGCCACAGCCGCAGC A C TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:24777037..24777162 26863196 MeRIP-seq:(Medium) rs1443272995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 66292 RMVar_ID_66292 Human_SNP_ID_598083964 m1A Human chr16 + 24790674 24790674 24790674 GAGGTACAGTGGAGAGCGATGGTAGTACAGAAAGCACTGGACGCCTTGAGGAAAAAGGAACTGGG GAGGTACAGTGGAGAGCGATGGTAGTACAGAATGCACTGGACGCCTTGAGGAAAAAGGAACTGGG A T TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24790623..24790735 26863196 MeRIP-seq:(Medium) rs373247119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5726,Human_RBP_ID_818353,Human_RBP_ID_5524233,Human_RBP_ID_12700402,Human_RBP_ID_18675744 Human_miRNA_ID_327330,Human_miRNA_ID_331354,Human_miRNA_ID_348449,Human_miRNA_ID_1511486,Human_miRNA_ID_1641712,Human_miRNA_ID_1755622,Human_miRNA_ID_2843810 RMVar_hsa_circ_26748,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_177406,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_71651,RMVar_hsa_circ_45427,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_269018,RMVar_hsa_circ_368747,RMVar_hsa_circ_177409,RMVar_hsa_circ_351298 66293 RMVar_ID_66293 Human_SNP_ID_598083967 m1A Human chr16 + 24790682 24790682 24790682 GTGGAGAGCGATGGTAGTACAGAAAGCACTGGACGCCTTGAGGAAAAAGGAACTGGGGAAAGTCA GTGGAGAGCGATGGTAGTACAGAAAGCACTGGGCGCCTTGAGGAAAAAGGAACTGGGGAAAGTCA A G TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:24790635..24790730 26863196 MeRIP-seq:(Medium) rs200216939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818353,Human_RBP_ID_6503343,Human_RBP_ID_12700402,Human_RBP_ID_17689919,Human_RBP_ID_18675744,Human_RBP_ID_26329925 Human_miRNA_ID_657429,Human_miRNA_ID_1755622,Human_miRNA_ID_2999458 RMVar_hsa_circ_26748,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_177406,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_71651,RMVar_hsa_circ_45427,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_269018,RMVar_hsa_circ_368747,RMVar_hsa_circ_177409,RMVar_hsa_circ_351298 66294 RMVar_ID_66294 Human_SNP_ID_598084151 m1A Human chr16 - 24791097 24791097 24791097 CCATGCAGCCTTCTCCTCTTTGCAATTCCCCCACTGATTGCTCTTGACCATTCCTGTAGCAGCAG CCATGCAGCCTTCTCCTCTTTGCAATTCCCCCCCTGATTGCTCTTGACCATTCCTGTAGCAGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:24791050..24791152 26863196 MeRIP-seq:(Medium) rs1250709836 Functional Loss SNV dbSNP153 33..33 33 - - - 66295 RMVar_ID_66295 Human_SNP_ID_598092497 m1A Human chr16 - 24821502 24821502 24821502 CCTCACAAACACTTCAGGTGCTGGGAAAGACCATTCCATGACACAGCTCAGGCCTATCCACCTCT CCTCACAAACACTTCAGGTGCTGGGAAAGACCGTTCCATGACACAGCTCAGGCCTATCCACCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24821451..24821613 26863196 MeRIP-seq:(Medium) rs902341305 Functional Loss SNV dbSNP153 33..33 33 - - - 66296 RMVar_ID_66296 Human_SNP_ID_598121433 m1A Human chr16 - 24931056 24931056 24931056 CCCCATGGCATTGCCCAGTGAGCATGGACTTGAGCAGCCATCTCACACCCCTCCCCAGACTCCAA CCCCATGGCATTGCCCAGTGAGCATGGACTTGGGCAGCCATCTCACACCCCTCCCCAGACTCCAA T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:24929639..24931352 26863196 MeRIP-seq:(Medium) rs1438989079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471184,Human_RBP_ID_5128555,Human_RBP_ID_12701453,Human_RBP_ID_17078165,Human_RBP_ID_17371344,Human_RBP_ID_18940100 Human_miRNA_ID_196264,Human_miRNA_ID_696942,Human_miRNA_ID_701877,Human_miRNA_ID_2153638,Human_miRNA_ID_2801515,Human_miRNA_ID_3009648 RMVar_hsa_circ_4748,RMVar_hsa_circ_115956,RMVar_hsa_circ_353833,RMVar_hsa_circ_177426 66297 RMVar_ID_66297 Human_SNP_ID_598141862 m1A Human chr16 - 25015162 25015147 25015162 CAGCACGGGGGTCGCACCGGGGCTGGGGGCGGAGGGCGGAGGGCGCGGGGGCGGGACGGCTCCTC CAGCACGGGGGTCGCACCGGGGCTGGGGGCGG_______________GGGGCGGGACGGCTCCTC CCGCGCCCTCCGCCCT C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:25015155..25015259 32194978 MeRIP-seq:(Medium) rs1394952880 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_233712,Human_RBP_ID_817241,Human_RBP_ID_5357828,Human_RBP_ID_8184446,Human_RBP_ID_9325017,Human_RBP_ID_9419163,Human_RBP_ID_18459084,Human_RBP_ID_19073820,Human_RBP_ID_26780295 RMVar_hsa_circ_112515,RMVar_hsa_circ_177438 66298 RMVar_ID_66298 Human_SNP_ID_598141865 m1A Human chr16 - 25015162 25015148 25015162 CAGCACGGGGGTCGCACCGGGGCTGGGGGCGGAGGGCGGAGGGCGCGGGGGCGGGACGGCTCCTC CAGCACGGGGGTCGCACCGGGGCTGGGGGCGG______________GGGGGCGGGACGGCTCCTC CGCGCCCTCCGCCCT C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:25015155..25015259 32194978 MeRIP-seq:(Medium) rs1335288302 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_233712,Human_RBP_ID_817241,Human_RBP_ID_5357828,Human_RBP_ID_8184446,Human_RBP_ID_9325017,Human_RBP_ID_9419163,Human_RBP_ID_18459084,Human_RBP_ID_19073820,Human_RBP_ID_26780295 RMVar_hsa_circ_112515,RMVar_hsa_circ_177438 66299 RMVar_ID_66299 Human_SNP_ID_598141873 m1A Human chr16 - 25015162 25015162 25015162 CAGCACGGGGGTCGCACCGGGGCTGGGGGCGGAGGGCGGAGGGCGCGGGGGCGGGACGGCTCCTC CAGCACGGGGGTCGCACCGGGGCTGGGGGCGGGGGGCGGAGGGCGCGGGGGCGGGACGGCTCCTC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:25015155..25015259 32194978 MeRIP-seq:(Medium) rs1451907659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233712,Human_RBP_ID_817241,Human_RBP_ID_5357828,Human_RBP_ID_8184446,Human_RBP_ID_9325017,Human_RBP_ID_9419163,Human_RBP_ID_18459084,Human_RBP_ID_19073820,Human_RBP_ID_26780295 RMVar_hsa_circ_112515,RMVar_hsa_circ_177438 66300 RMVar_ID_66300 Human_SNP_ID_598146758 m1A Human chr16 + 25031821 25031821 25031821 CTGCTTTCTGCCTGTGACTAGCGCCGTCCCCTACCGCCCGTCGACCCCACTTCCATGTCTGGCGG CTGCTTTCTGCCTGTGACTAGCGCCGTCCCCTGCCGCCCGTCGACCCCACTTCCATGTCTGGCGG A G AC133552.2 Ensembl:ENSG00000262587 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:25031773..25031907 26863196 MeRIP-seq:(Medium) rs551671695 Functional Loss SNV dbSNP153 33..33 33 - - - 66301 RMVar_ID_66301 Human_SNP_ID_598146869 m1A Human chr16 + 25032042 25032042 25032042 GGATTCGGGGCTGGCATCTGGGACGCGGGCTGAGGTGGGAGGCGGGCCTGCATCTGAAGAATACG GGATTCGGGGCTGGCATCTGGGACGCGGGCTGTGGTGGGAGGCGGGCCTGCATCTGAAGAATACG A T AC133552.2 Ensembl:ENSG00000262587 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:25031992..25032096 26863196 MeRIP-seq:(Medium) rs1472558198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573448 66302 RMVar_ID_66302 Human_SNP_ID_598167170 m1A Human chr16 - 25111847 25111847 25111847 GTGGAGGTTCCTGGGAGCTGTGTCCGCCAGGGACATGGAAGCGGGGTCGACGGGCGGCGGGGGAC GTGGAGGTTCCTGGGAGCTGTGTCCGCCAGGGCCATGGAAGCGGGGTCGACGGGCGGCGGGGGAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:25111799..25111916 26863196 MeRIP-seq:(Medium) rs761603226 Functional Loss SNV dbSNP153 33..33 33 - - - 66303 RMVar_ID_66303 Human_SNP_ID_598171607 m1A Human chr16 + 25128438 25128438 25128438 CTTGGCAGTGGACCTTGGTCTGAACCTACTCAATCTCTACTCACCTTCCTCCTTTTTTCTCCCTT CTTGGCAGTGGACCTTGGTCTGAACCTACTCAGTCTCTACTCACCTTCCTCCTTTTTTCTCCCTT A G LCMT1 Ensembl:ENSG00000205629 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:25128431..25128500 26863196 MeRIP-seq:(Medium) rs939586852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891770,Human_RBP_ID_22542303,Human_RBP_ID_22651849 RMVar_hsa_circ_99021,RMVar_hsa_circ_177440 66304 RMVar_ID_66304 Human_SNP_ID_598181832 m1A Human chr16 - 25169176 25169176 25169176 ACTCTAATGACTTGCAGGTCTCCACTCCCGCCAGGTCACACTGGCGTCTCCGCAGGTTTTCAATC ACTCTAATGACTTGCAGGTCTCCACTCCCGCCGGGTCACACTGGCGTCTCCGCAGGTTTTCAATC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:25169126..25169175 32194978 MeRIP-seq:(Medium) rs776945285 Functional Loss SNV dbSNP153 33..33 33 - - - 66305 RMVar_ID_66305 Human_SNP_ID_598183292 m1A Human chr16 + 25174880 25174880 25174880 TAAACATTTTTTCATATCCGTAGCTATGGGCCATGATCTTCATTTTCAATGCAGACACTTGCATC TAAACATTTTTTCATATCCGTAGCTATGGGCCGTGATCTTCATTTTCAATGCAGACACTTGCATC A G LCMT1 Ensembl:ENSG00000205629 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:25174877..25174963;chr16:25174874..25174964 26863196 MeRIP-seq:(Medium) rs188409247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99021,RMVar_hsa_circ_177440,RMVar_hsa_circ_115718,RMVar_hsa_circ_19296,RMVar_hsa_circ_177441,RMVar_hsa_circ_52335,RMVar_hsa_circ_119792,RMVar_hsa_circ_177448,RMVar_hsa_circ_86148,RMVar_hsa_circ_177451,RMVar_hsa_circ_341896,RMVar_hsa_circ_177453,RMVar_hsa_circ_114759,RMVar_hsa_circ_320673,RMVar_hsa_circ_177452,RMVar_hsa_circ_177456,RMVar_hsa_circ_177457,RMVar_hsa_circ_290247 66306 RMVar_ID_66306 Human_SNP_ID_598200873 m1A Human chr16 - 25238823 25238823 25238823 GCACTGCAGTATAATATTATAATAGTGTTTCTAAAACTTTAAGGGGATAGGGAAGAGGTAATAGA GCACTGCAGTATAATATTATAATAGTGTTTCTGAAACTTTAAGGGGATAGGGAAGAGGTAATAGA T C ZKSCAN2 Ensembl:ENSG00000155592 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72771346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1003630,Human_RBP_ID_27657731 GWAS_ID_7947,GWAS_ID_7948,GWAS_ID_7949,GWAS_ID_7950,GWAS_ID_7951 66307 RMVar_ID_66307 Human_SNP_ID_598206315 m1A Human chr16 + 25258131 25258131 25258131 TAGGCGGCGGCGGGGCCTCCCTGAGGCGGAGGAGTCGGCACCGGGGCCTGGCTGCCGGGGAAGGA TAGGCGGCGGCGGGGCCTCCCTGAGGCGGAGGCGTCGGCACCGGGGCCTGGCTGCCGGGGAAGGA A C ZKSCAN2-DT Ensembl:ENSG00000274925 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:25258080..25258219 26863196 MeRIP-seq:(Medium) rs952925019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21971195,Human_RBP_ID_26780297 66308 RMVar_ID_66308 Human_SNP_ID_598206971 m1A Human chr16 + 25259943 25259943 25259943 GTCGTCAGGTGTCCTTAATGAAGGGGCTGGGCATTAAGAGCAAGGCGAGGAGGCAGAAGGAAAGC GTCGTCAGGTGTCCTTAATGAAGGGGCTGGGCGTTAAGAGCAAGGCGAGGAGGCAGAAGGAAAGC A G ZKSCAN2-DT Ensembl:ENSG00000274925 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:25259892..25259986 26863196 MeRIP-seq:(Medium) rs959896425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12703417,Human_RBP_ID_25201178 66309 RMVar_ID_66309 Human_SNP_ID_598395158 m1A Human chr16 - 26032691 26032691 26032691 CTAAACCTGCTCCTCCAAAGCCAGAGCCCAAGACTAAAAAGGCCCCTGCAAAGAAGGGAGAGAAG CTAAACCTGCTCCTCCAAAGCCAGAGCCCAAGCCTAAAAAGGCCCCTGCAAAGAAGGGAGAGAAG T G HMGN2P3 Ensembl:ENSG00000230330 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1463528955 Functional Loss SNV dbSNP153 33..33 33 - - - 66310 RMVar_ID_66310 Human_SNP_ID_598613801 m1A Human chr16 + 26862373 26862373 26862373 AAGCAAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAAAAGAAAAAATCAAATCTAAATCTAATC AAGCAAGACCCTGTCTCCAAAAAAAAAAAAAACAAGAAAAGAAAAAATCAAATCTAAATCTAATC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:26862355..26862439 26863410 MeRIP-seq:(Medium) rs985946808 Functional Loss SNV dbSNP153 33..33 33 - - - 66311 RMVar_ID_66311 Human_SNP_ID_598684524 m1A Human chr16 + 27134717 27134717 27134717 TCTTCTGGCCATAGGGTGGCTCGGTGGAATCCATTTTGTGAACACCAACAATTAGTTGTTTCACA TCTTCTGGCCATAGGGTGGCTCGGTGGAATCCCTTTTGTGAACACCAACAATTAGTTGTTTCACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27134695..27134760 26863196 MeRIP-seq:(Medium) rs370722825 Functional Loss SNV dbSNP153 33..33 33 - - - 66312 RMVar_ID_66312 Human_SNP_ID_598686582 m1A Human chr16 + 27139359 27139353 27139359 ATGATGGTGGTGATGGTGATGGTGGTGATGGTAGTGGTGATGGTAGTGATAAGGGTGATAATGAT ATGATGGTGGTGATGGTGATGGTGGTG______GTGGTGATGGTAGTGATAAGGGTGATAATGAT GATGGTA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:27139323..27139407 26863196 MeRIP-seq:(Medium) rs200862474 Functional Loss DEL dbSNP153 28..33 33 - - - 66313 RMVar_ID_66313 Human_SNP_ID_598686585 m1A Human chr16 + 27139359 27139359 27139359 ATGATGGTGGTGATGGTGATGGTGGTGATGGTAGTGGTGATGGTAGTGATAAGGGTGATAATGAT ATGATGGTGGTGATGGTGATGGTGGTGATGGTGGTGGTGATGGTAGTGATAAGGGTGATAATGAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:27139323..27139407 26863196 MeRIP-seq:(Medium) rs978798568 Functional Loss SNV dbSNP153 33..33 33 - - - 66314 RMVar_ID_66314 Human_SNP_ID_598705622 m1A Human chr16 - 27216259 27216259 27216259 CCACCTGCCAGCATCACCTCTCCTTGCACCACAGCAATAGCCCAGCCAGCCACCCGCTCCGACAG CCACCTGCCAGCATCACCTCTCCTTGCACCACGGCAATAGCCCAGCCAGCCACCCGCTCCGACAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27216254..27216319 26863196 MeRIP-seq:(Medium) rs1014316244 Functional Loss SNV dbSNP153 33..33 33 - - - 66315 RMVar_ID_66315 Human_SNP_ID_598708212 m1A Human chr16 - 27225812 27225812 27225812 TCAAAGCTGCGAAACCTGTGGGATCAGGATGCACTTACCCTGCGTGGCCAAGTACTTCCAGTCGA TCAAAGCTGCGAAACCTGTGGGATCAGGATGCGCTTACCCTGCGTGGCCAAGTACTTCCAGTCGA T C NSMCE1 Ensembl:ENSG00000169189 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:27225751..27225850 32194978 MeRIP-seq:(Medium) rs751348142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4359165,Human_RBP_ID_18676129 Human_Splice_Rec_1694252,Human_Splice_Rec_1694253,Human_Splice_Rec_1694270,Human_Splice_Rec_1694271,Human_Splice_Rec_1694283,Human_Splice_Rec_1694288,Human_Splice_Rec_1694289 Human_miRNA_ID_1347390,Human_miRNA_ID_1809986,Human_miRNA_ID_2675668,Human_miRNA_ID_2806348,Human_miRNA_ID_2809491,Human_miRNA_ID_2812632,Human_miRNA_ID_2926419 RMVar_hsa_circ_177479,RMVar_hsa_circ_83767,RMVar_hsa_circ_106989,RMVar_hsa_circ_115794,RMVar_hsa_circ_111820,RMVar_hsa_circ_90467,RMVar_hsa_circ_79464,RMVar_hsa_circ_80068,RMVar_hsa_circ_177481,RMVar_hsa_circ_177482,RMVar_hsa_circ_177483,RMVar_hsa_circ_177480,RMVar_hsa_circ_177477,RMVar_hsa_circ_177478 66316 RMVar_ID_66316 Human_SNP_ID_598712901 m1A Human chr16 + 27244656 27244655 27244656 ATCACCCGAGCATCGCCACATATGGCAGCTCCACAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG ATCACCCGAGCATCGCCACATATGGCAGCTCC_CAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27244652..27244731 26863196 MeRIP-seq:(Medium) rs35986918 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_7952,GWAS_ID_7953,GWAS_ID_7954,GWAS_ID_7955,GWAS_ID_7956,GWAS_ID_7957,GWAS_ID_7958,GWAS_ID_7959,GWAS_ID_7960,GWAS_ID_7961,GWAS_ID_7962,GWAS_ID_7963 66317 RMVar_ID_66317 Human_SNP_ID_598712904 m1A Human chr16 + 27244656 27244656 27244656 ATCACCCGAGCATCGCCACATATGGCAGCTCCACAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG ATCACCCGAGCATCGCCACATATGGCAGCTCCCCAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27244652..27244731 26863196 MeRIP-seq:(Medium) rs200340307 Functional Loss SNV dbSNP153 33..33 33 - - - 66318 RMVar_ID_66318 Human_SNP_ID_598715933 m1A Human chr16 - 27257556 27257556 27257556 TTTTCAGTTCGTTCCCACATGCAGGGCAGCACAAGGAGAATGGGCGTCATGACTGATGTCCACCG TTTTCAGTTCGTTCCCACATGCAGGGCAGCACGAGGAGAATGGGCGTCATGACTGATGTCCACCG T C NSMCE1 Ensembl:ENSG00000169189 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:27257451..27257600 32194978 MeRIP-seq:(Medium) rs762396205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234116,Human_RBP_ID_891777,Human_RBP_ID_4359188 Human_Splice_Rec_1694242,Human_Splice_Rec_1694258,Human_Splice_Rec_1694274,Human_Splice_Rec_1694296,Human_Splice_Rec_1694310,Human_Splice_Rec_1694320,Human_Splice_Rec_1694328,Human_Splice_Rec_1694336,Human_Splice_Rec_1694344,Human_Splice_Rec_1694350,Human_Splice_Rec_1694356 RMVar_hsa_circ_106989,RMVar_hsa_circ_90467,RMVar_hsa_circ_80068,RMVar_hsa_circ_177481,RMVar_hsa_circ_177482,RMVar_hsa_circ_177483,RMVar_hsa_circ_63111 66319 RMVar_ID_66319 Human_SNP_ID_598718400 m1A Human chr16 - 27268652 27268652 27268652 GGGTTGGAGGGGAAAGAAGAGGGACTTCAAGGAAGGCGAGGGGAGGACGGAAGGTGGGGTGGGCG GGGTTGGAGGGGAAAGAAGAGGGACTTCAAGGTAGGCGAGGGGAGGACGGAAGGTGGGGTGGGCG T A NSMCE1 Ensembl:ENSG00000169189 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:27268649..27268721 26863196 MeRIP-seq:(Medium) rs1241963322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418967 RMVar_hsa_circ_90467,RMVar_hsa_circ_177483 66320 RMVar_ID_66320 Human_SNP_ID_598729757 m1A Human chr16 + 27313670 27313669 27313671 CGTTTTATTCCGAGACCAAGGGGATCCACTGCAGAGTTCTCCGCTGGGCGTGACCTCGGGCTACG CGTTTTATTCCGAGACCAAGGGGATCCACTGC__AGTTCTCCGCTGGGCGTGACCTCGGGCTACG CAG C IL4R Ensembl:ENSG00000077238 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:27313576..27313792 26863196 MeRIP-seq:(Medium) rs1187504932 Functional Loss DEL dbSNP153 33..34 33 - - - 66321 RMVar_ID_66321 Human_SNP_ID_598729758 m1A Human chr16 + 27313670 27313670 27313670 CGTTTTATTCCGAGACCAAGGGGATCCACTGCAGAGTTCTCCGCTGGGCGTGACCTCGGGCTACG CGTTTTATTCCGAGACCAAGGGGATCCACTGCGGAGTTCTCCGCTGGGCGTGACCTCGGGCTACG A G IL4R Ensembl:ENSG00000077238 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:27313576..27313792 26863196 MeRIP-seq:(Medium) rs376195936 Functional Loss SNV dbSNP153 33..33 33 - - - 66322 RMVar_ID_66322 Human_SNP_ID_598741781 m1A Human chr16 - 27362433 27362433 27362433 ACACTCCACCGGGGCCTCAAACAACTCCACACATCGCACCACGCTGATGCTCTCTGGCCAGAGGA ACACTCCACCGGGGCCTCAAACAACTCCACACGTCGCACCACGCTGATGCTCTCTGGCCAGAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27362382..27362698 26863196 MeRIP-seq:(Medium) rs200547374 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 66323 RMVar_ID_66323 Human_SNP_ID_598766752 m1A Human chr16 - 27461370 27461370 27461370 TGGGCCGTGTGTTCCCCCACGAGGTCAACTGGAACAAGTGGATCCACCTCTAGGACCCCTGTGGG TGGGCCGTGTGTTCCCCCACGAGGTCAACTGGGACAAGTGGATCCACCTCTAGGACCCCTGTGGG T C GTF3C1 Ensembl:ENSG00000077235 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:27461322..27461476 26863196 MeRIP-seq:(Medium) rs776527254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089509,Human_RBP_ID_17653329,Human_RBP_ID_27239516,Human_RBP_ID_27440649 Human_miRNA_ID_2071098,Human_miRNA_ID_2804020 RMVar_hsa_circ_177505,RMVar_hsa_circ_88491,RMVar_hsa_circ_115330,RMVar_hsa_circ_127790,RMVar_hsa_circ_97019,RMVar_hsa_circ_79127,RMVar_hsa_circ_83210,RMVar_hsa_circ_177507,RMVar_hsa_circ_177509,RMVar_hsa_circ_77445,RMVar_hsa_circ_177508,RMVar_hsa_circ_177506,RMVar_hsa_circ_177503,RMVar_hsa_circ_177504 66324 RMVar_ID_66324 Human_SNP_ID_598772048 m1A Human chr16 + 27481480 27481480 27481480 CACCCTGCATCGCTGGCACTCTCCCAAGCCCCAGGTGAGATGACTCAAACGTGCCCCACACAGTG CACCCTGCATCGCTGGCACTCTCCCAAGCCCCCGGTGAGATGACTCAAACGTGCCCCACACAGTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:27481445..27481580 26863196 MeRIP-seq:(Medium) rs1200904814 Functional Loss SNV dbSNP153 33..33 33 - - - 66325 RMVar_ID_66325 Human_SNP_ID_598782285 m1A Human chr16 + 27521331 27521331 27521331 ATCAGCTAGCTACACCTTAGAGAGGTCTTGCGAGAAAATCTTAGGGCCTCTCCCTCAGCGTGTGG ATCAGCTAGCTACACCTTAGAGAGGTCTTGCGGGAAAATCTTAGGGCCTCTCCCTCAGCGTGTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:27521328..27521434 26863196 MeRIP-seq:(Medium) rs1436289320 Functional Loss SNV dbSNP153 33..33 33 - - - 66326 RMVar_ID_66326 Human_SNP_ID_598784626 m1A Human chr16 - 27530904 27530902 27530905 TGCCTGCACTGGGATGTAGAGGTGACTGAAGAAGGAGGATCTCGAGATGAAGCCAGTGAGTTTCG TGCCTGCACTGGGATGTAGAGGTGACTGAAG___GAGGATCTCGAGATGAAGCCAGTGAGTTTCG CCTT C GTF3C1 Ensembl:ENSG00000077235 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:27530902..27531027 26863196 MeRIP-seq:(Medium) rs1280536279 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12707072 RMVar_hsa_circ_127790,RMVar_hsa_circ_177503,RMVar_hsa_circ_113504,RMVar_hsa_circ_177515,RMVar_hsa_circ_100819,RMVar_hsa_circ_177514,RMVar_hsa_circ_104243,RMVar_hsa_circ_127911,RMVar_hsa_circ_126676,RMVar_hsa_circ_177525,RMVar_hsa_circ_177526,RMVar_hsa_circ_177524,RMVar_hsa_circ_266117,RMVar_hsa_circ_177530,RMVar_hsa_circ_8292,RMVar_hsa_circ_177529,RMVar_hsa_circ_113429,RMVar_hsa_circ_357263,RMVar_hsa_circ_273829,RMVar_hsa_circ_325240,RMVar_hsa_circ_343056,RMVar_hsa_circ_177531 66327 RMVar_ID_66327 Human_SNP_ID_598789500 m1A Human chr16 - 27549861 27549861 27549861 GCAATGGACGCGCTGGAGTCGTTGTTGGACGAAGTCGCTCTGGAGGGGCTCGATGGCCTGTGTCT GCAATGGACGCGCTGGAGTCGTTGTTGGACGAGGTCGCTCTGGAGGGGCTCGATGGCCTGTGTCT T C GTF3C1 Ensembl:ENSG00000077235 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27549712..27549900 26863196 MeRIP-seq:(Medium) rs145978655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471439,Human_RBP_ID_760546,Human_RBP_ID_1515358,Human_RBP_ID_4394517,Human_RBP_ID_8806208,Human_RBP_ID_9256948,Human_RBP_ID_9285718,Human_RBP_ID_9374093,Human_RBP_ID_22054537,Human_RBP_ID_22441877,Human_RBP_ID_26328112 RMVar_hsa_circ_127790,RMVar_hsa_circ_177503,RMVar_hsa_circ_104243,RMVar_hsa_circ_177526,RMVar_hsa_circ_266117 66328 RMVar_ID_66328 Human_SNP_ID_598789501 m1A Human chr16 - 27549861 27549861 27549861 GCAATGGACGCGCTGGAGTCGTTGTTGGACGAAGTCGCTCTGGAGGGGCTCGATGGCCTGTGTCT GCAATGGACGCGCTGGAGTCGTTGTTGGACGACGTCGCTCTGGAGGGGCTCGATGGCCTGTGTCT T G GTF3C1 Ensembl:ENSG00000077235 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27549712..27549900 26863196 MeRIP-seq:(Medium) rs145978655 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_471439,Human_RBP_ID_760546,Human_RBP_ID_1515358,Human_RBP_ID_4394517,Human_RBP_ID_8806208,Human_RBP_ID_9256948,Human_RBP_ID_9285718,Human_RBP_ID_9374093,Human_RBP_ID_22054537,Human_RBP_ID_22441877,Human_RBP_ID_26328112 RMVar_hsa_circ_127790,RMVar_hsa_circ_177503,RMVar_hsa_circ_104243,RMVar_hsa_circ_177526,RMVar_hsa_circ_266117 66329 RMVar_ID_66329 Human_SNP_ID_598790615 m1A Human chr16 + 27554003 27554002 27554003 GGGTGGGGGGAGAGAGGAGAGAGAAAGGAAGGAAGGAAAGAAGGGAGGGAGAGGAGAGAGAAAGG GGGTGGGGGGAGAGAGGAGAGAGAAAGGAAGG_AGGAAAGAAGGGAGGGAGAGGAGAGAGAAAGG GA G KIAA0556 Ensembl:ENSG00000047578 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27554001..27554107 26863196 MeRIP-seq:(Medium) rs1300253773 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_108706,RMVar_hsa_circ_177536 66330 RMVar_ID_66330 Human_SNP_ID_598795398 m1A Human chr16 + 27573951 27573951 27573951 CCGAGAGAAGCTGGTCCTGCTCACGAGAGAAAAAGGAGGTAAATGTGTCCCTGGCGAGGGCTGAT CCGAGAGAAGCTGGTCCTGCTCACGAGAGAAACAGGAGGTAAATGTGTCCCTGGCGAGGGCTGAT A C KIAA0556 Ensembl:ENSG00000047578 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27573945..27574013 26863196 MeRIP-seq:(Medium) rs1347036908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1694812,Human_Splice_Rec_1694814,Human_Splice_Rec_1694815,Human_Splice_Rec_1694867,Human_Splice_Rec_1694879 RMVar_hsa_circ_108706,RMVar_hsa_circ_177536 66331 RMVar_ID_66331 Human_SNP_ID_598803990 m1A Human chr16 - 27609893 27609893 27609893 TTCCTCCTTCAAGACTTAACCCACTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAA TTCCTCCTTCAAGACTTAACCCACTGGCCAACGTGGTGAAACCTCATCTCTACTAAAAATACAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:27609883..27610160 26863196 MeRIP-seq:(Medium) rs1261852652 Functional Loss SNV dbSNP153 33..33 33 - - - 66332 RMVar_ID_66332 Human_SNP_ID_598922110 m1A Human chr16 + 28089178 28089174 28089179 ACCACACACAAACCACACACCCCCACATACACACCACACACCCCACACACACCACACACCCACAC ACCACACACAAACCACACACCCCCACATA_____CACACACCCCACACACACCACACACCCACAC ACACAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28089168..28089365 26863196 MeRIP-seq:(Medium) rs1456471067 Functional Loss DEL dbSNP153 30..34 33 - - - 66333 RMVar_ID_66333 Human_SNP_ID_598922111 m1A Human chr16 + 28089178 28089176 28089179 ACCACACACAAACCACACACCCCCACATACACACCACACACCCCACACACACCACACACCCACAC ACCACACACAAACCACACACCCCCACATACA___CACACACCCCACACACACCACACACCCACAC ACAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28089168..28089365 26863196 MeRIP-seq:(Medium) rs1409314397 Functional Loss DEL dbSNP153 32..34 33 - - - 66334 RMVar_ID_66334 Human_SNP_ID_598922113 m1A Human chr16 + 28089178 28089178 28089178 ACCACACACAAACCACACACCCCCACATACACACCACACACCCCACACACACCACACACCCACAC ACCACACACAAACCACACACCCCCACATACACCCCACACACCCCACACACACCACACACCCACAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28089168..28089365 26863196 MeRIP-seq:(Medium) rs1160848942 Functional Loss SNV dbSNP153 33..33 33 - - - 66335 RMVar_ID_66335 Human_SNP_ID_598924655 m1A Human chr16 - 28097075 28097075 28097075 GGGGCTGGGCCGGGGTGAGCAGGGCGTGCATGATGTGTGCTTGTGTGGCAGGCCCTCGTCCATGT GGGGCTGGGCCGGGGTGAGCAGGGCGTGCATGTTGTGTGCTTGTGTGGCAGGCCCTCGTCCATGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28097027..28097115 26863196 MeRIP-seq:(Medium) rs1260212110 Functional Loss SNV dbSNP153 33..33 33 - - - 66336 RMVar_ID_66336 Human_SNP_ID_598924963 m1A Human chr16 + 28098301 28098301 28098301 GGATTTCCTGGTGCCTCCTAGTACCTGGCCACACACCCCTCCGCCTGCTCCAACGCCCTGGGAGC GGATTTCCTGGTGCCTCCTAGTACCTGGCCACGCACCCCTCCGCCTGCTCCAACGCCCTGGGAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28098251..28098450 32194978 MeRIP-seq:(Medium) rs1056650024 Functional Loss SNV dbSNP153 33..33 33 - - - 66337 RMVar_ID_66337 Human_SNP_ID_598924987 m1A Human chr16 - 28098373 28098373 28098373 CTCTGCCGCTCCTCCACATCTTGCCGCTGCCCAGCAGAGCTGGCTTCTGGGTCCACCTGAGCACT CTCTGCCGCTCCTCCACATCTTGCCGCTGCCCTGCAGAGCTGGCTTCTGGGTCCACCTGAGCACT T A XPO6 Ensembl:ENSG00000169180 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:28098326..28101090 32194978 MeRIP-seq:(Medium) rs1424668489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445949,Human_RBP_ID_26810146,Human_RBP_ID_27440719 Human_miRNA_ID_880790,Human_miRNA_ID_883555,Human_miRNA_ID_2395881 RMVar_hsa_circ_177561,RMVar_hsa_circ_103755 66338 RMVar_ID_66338 Human_SNP_ID_598925020 m1A Human chr16 + 28098502 28098499 28098502 CTGTGGTGGAAGGTAGGGCTGGCGCAGGTGGCAGCAGCAGAAGTCCGTGTCCCCAGGCAGTAGCA CTGTGGTGGAAGGTAGGGCTGGCGCAGGTG___GCAGCAGAAGTCCGTGTCCCCAGGCAGTAGCA GGCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28098451..28098625 32194978 MeRIP-seq:(Medium) rs764519581 Functional Loss DEL dbSNP153 31..33 33 - - - 66339 RMVar_ID_66339 Human_SNP_ID_598925032 m1A Human chr16 - 28098530 28098530 28098530 GCCCCCTGGCACTGTGAAGCTCTAGGCCTGCTACTGCCTGGGGACACGGACTTCTGCTGCTGCCA GCCCCCTGGCACTGTGAAGCTCTAGGCCTGCTGCTGCCTGGGGACACGGACTTCTGCTGCTGCCA T C XPO6 Ensembl:ENSG00000169180 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28098481..28098582 26863196 MeRIP-seq:(Medium) rs1459620605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4397929,Human_RBP_ID_5180615,Human_RBP_ID_6505222,Human_RBP_ID_8806251,Human_RBP_ID_9286200,Human_RBP_ID_17257056,Human_RBP_ID_17371678,Human_RBP_ID_18437389,Human_RBP_ID_22053998,Human_RBP_ID_27440723 Human_Splice_Rec_1695068 Human_miRNA_ID_2258063,Human_miRNA_ID_2280306,Human_miRNA_ID_2460369,Human_miRNA_ID_2640583 RMVar_hsa_circ_177561,RMVar_hsa_circ_103755 66340 RMVar_ID_66340 Human_SNP_ID_598925033 m1A Human chr16 - 28098530 28098530 28098530 GCCCCCTGGCACTGTGAAGCTCTAGGCCTGCTACTGCCTGGGGACACGGACTTCTGCTGCTGCCA GCCCCCTGGCACTGTGAAGCTCTAGGCCTGCTCCTGCCTGGGGACACGGACTTCTGCTGCTGCCA T G XPO6 Ensembl:ENSG00000169180 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28098481..28098582 26863196 MeRIP-seq:(Medium) rs1459620605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4397929,Human_RBP_ID_5180615,Human_RBP_ID_6505222,Human_RBP_ID_8806251,Human_RBP_ID_9286200,Human_RBP_ID_17257056,Human_RBP_ID_17371678,Human_RBP_ID_18437389,Human_RBP_ID_22053998,Human_RBP_ID_27440723 Human_Splice_Rec_1695068 Human_miRNA_ID_2258063,Human_miRNA_ID_2280306,Human_miRNA_ID_2460369,Human_miRNA_ID_2640583 RMVar_hsa_circ_177561,RMVar_hsa_circ_103755 66341 RMVar_ID_66341 Human_SNP_ID_598938748 m1A Human chr16 - 28156462 28156462 28156462 GTTCAGCCAAACTGTTGAATCAGCCAATTCCCATCCTTGATGTGGAGAGTGAGTATATCTGTTCC GTTCAGCCAAACTGTTGAATCAGCCAATTCCCGTCCTTGATGTGGAGAGTGAGTATATCTGTTCC T C XPO6 Ensembl:ENSG00000169180 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:28156414..28156514 32194978 MeRIP-seq:(Medium) rs902852483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1281589,Human_RBP_ID_1840831,Human_RBP_ID_8806535,Human_RBP_ID_18676652,Human_RBP_ID_23685295,Human_RBP_ID_27239743 Human_Splice_Rec_1695030,Human_Splice_Rec_1695080,Human_Splice_Rec_1695204,Human_Splice_Rec_1695212,Human_Splice_Rec_1695218 Human_miRNA_ID_2903010 RMVar_hsa_circ_42265,RMVar_hsa_circ_81172,RMVar_hsa_circ_177561,RMVar_hsa_circ_103755,RMVar_hsa_circ_108269,RMVar_hsa_circ_177562,RMVar_hsa_circ_177563,RMVar_hsa_circ_99501,RMVar_hsa_circ_177572,RMVar_hsa_circ_110257,RMVar_hsa_circ_34243,RMVar_hsa_circ_106028,RMVar_hsa_circ_177576,RMVar_hsa_circ_177580,RMVar_hsa_circ_107367,RMVar_hsa_circ_18503,RMVar_hsa_circ_318775,RMVar_hsa_circ_177589,RMVar_hsa_circ_113397,RMVar_hsa_circ_177594,RMVar_hsa_circ_346263,RMVar_hsa_circ_373888,RMVar_hsa_circ_375742,RMVar_hsa_circ_10534,RMVar_hsa_circ_177595,RMVar_hsa_circ_177596,RMVar_hsa_circ_363728,RMVar_hsa_circ_177601,RMVar_hsa_circ_378642,RMVar_hsa_circ_288466,RMVar_hsa_circ_123592,RMVar_hsa_circ_177603,RMVar_hsa_circ_331374,RMVar_hsa_circ_85744,RMVar_hsa_circ_177606,RMVar_hsa_circ_177607,RMVar_hsa_circ_275764,RMVar_hsa_circ_278757,RMVar_hsa_circ_368045,RMVar_hsa_circ_19492,RMVar_hsa_circ_41721,RMVar_hsa_circ_278549,RMVar_hsa_circ_177609,RMVar_hsa_circ_177610,RMVar_hsa_circ_313081,RMVar_hsa_circ_347408,RMVar_hsa_circ_34425,RMVar_hsa_circ_44421,RMVar_hsa_circ_90873,RMVar_hsa_circ_177611,RMVar_hsa_circ_177612,RMVar_hsa_circ_30851 66342 RMVar_ID_66342 Human_SNP_ID_598941155 m1A Human chr16 - 28166773 28166773 28166773 TGGGGAGAGGCCACACCACAAGGCCACAGTGAAGCAGTGGAGAGCCAGAAGATAGCTGTGAAGTC TGGGGAGAGGCCACACCACAAGGCCACAGTGAGGCAGTGGAGAGCCAGAAGATAGCTGTGAAGTC T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28166771..28166877 26863196 MeRIP-seq:(Medium) rs187059241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45460,Human_RBP_ID_26329951 RMVar_hsa_circ_81172,RMVar_hsa_circ_177561,RMVar_hsa_circ_103755,RMVar_hsa_circ_108269,RMVar_hsa_circ_177562,RMVar_hsa_circ_177563,RMVar_hsa_circ_99501,RMVar_hsa_circ_177572,RMVar_hsa_circ_110257,RMVar_hsa_circ_106028,RMVar_hsa_circ_177576,RMVar_hsa_circ_177580,RMVar_hsa_circ_107367,RMVar_hsa_circ_18503,RMVar_hsa_circ_177589,RMVar_hsa_circ_113397,RMVar_hsa_circ_177594,RMVar_hsa_circ_346263,RMVar_hsa_circ_375742,RMVar_hsa_circ_177595,RMVar_hsa_circ_363728,RMVar_hsa_circ_177601,RMVar_hsa_circ_378642,RMVar_hsa_circ_123592,RMVar_hsa_circ_85744,RMVar_hsa_circ_177606,RMVar_hsa_circ_177607,RMVar_hsa_circ_278757,RMVar_hsa_circ_368045,RMVar_hsa_circ_41721,RMVar_hsa_circ_177610,RMVar_hsa_circ_313081,RMVar_hsa_circ_347408,RMVar_hsa_circ_34425,RMVar_hsa_circ_90873,RMVar_hsa_circ_177615,RMVar_hsa_circ_177612,RMVar_hsa_circ_272235,RMVar_hsa_circ_285097,RMVar_hsa_circ_285248,RMVar_hsa_circ_278711,RMVar_hsa_circ_177616,RMVar_hsa_circ_177613,RMVar_hsa_circ_177614 66343 RMVar_ID_66343 Human_SNP_ID_598943120 m1A Human chr16 - 28175111 28175111 28175111 GGAATCTAGAATGACTTCCAGTTTTCTGGCTCAGATAGATTTTTCAGGCCAGGGTTGAAAGAAGG GGAATCTAGAATGACTTCCAGTTTTCTGGCTCGGATAGATTTTTCAGGCCAGGGTTGAAAGAAGG T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28175108..28175448 26863196 MeRIP-seq:(Medium) rs1156601569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12710568,Human_RBP_ID_22945621 RMVar_hsa_circ_108269,RMVar_hsa_circ_177562,RMVar_hsa_circ_110257,RMVar_hsa_circ_177576,RMVar_hsa_circ_113397,RMVar_hsa_circ_177594,RMVar_hsa_circ_375742,RMVar_hsa_circ_177595,RMVar_hsa_circ_378642,RMVar_hsa_circ_123592,RMVar_hsa_circ_177606,RMVar_hsa_circ_368045,RMVar_hsa_circ_41721,RMVar_hsa_circ_313081,RMVar_hsa_circ_34425,RMVar_hsa_circ_90873,RMVar_hsa_circ_177615,RMVar_hsa_circ_177612,RMVar_hsa_circ_272235,RMVar_hsa_circ_285097,RMVar_hsa_circ_285248,RMVar_hsa_circ_177616,RMVar_hsa_circ_177614,RMVar_hsa_circ_336098,RMVar_hsa_circ_353570,RMVar_hsa_circ_292998,RMVar_hsa_circ_177617 66344 RMVar_ID_66344 Human_SNP_ID_598951856 m1A Human chr16 + 28211477 28211477 28211477 TGGTCCCGGCAGACTCGGGAAGTCCCCCACCCATGCAAAGACAACCCCTTCCCCACCGGGCCCCG TGGTCCCGGCAGACTCGGGAAGTCCCCCACCCGTGCAAAGACAACCCCTTCCCCACCGGGCCCCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28211426..28211950 26863196 MeRIP-seq:(Medium) rs542034745 Functional Loss SNV dbSNP153 33..33 33 - - - 66345 RMVar_ID_66345 Human_SNP_ID_598952023 m1A Human chr16 - 28211918 28211918 28211918 GGGCTGTTGGTCGGGGGCGGCCGCGCGGTACTAGCGGGCGGCTCCAGGGCGGGCGCGCGCAAGGA GGGCTGTTGGTCGGGGGCGGCCGCGCGGTACTCGCGGGCGGCTCCAGGGCGGGCGCGCGCAAGGA T G XPO6 Ensembl:ENSG00000169180 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:28211638..28211975;chr16:28211601..28212000;chr16:28211633..28211975 26863196 MeRIP-seq:(Medium) rs1236735542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46314,Human_RBP_ID_4398123,Human_RBP_ID_5259181 66346 RMVar_ID_66346 Human_SNP_ID_599015238 m1A Human chr16 - 28486390 28486390 28486390 GCCTCACCCAGGCCGGCCTCTCCCCTCAGCAGACCCTGCTGTCCATGCTGGGTATCCCTGCCCTG GCCTCACCCAGGCCGGCCTCTCCCCTCAGCAGGCCCTGCTGTCCATGCTGGGTATCCCTGCCCTG T C AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28484028..28486407 32194978 MeRIP-seq:(Medium) rs1335425316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22441375,Human_RBP_ID_22759808 Human_Splice_Rec_1695373,Human_Splice_Rec_1695417,Human_Splice_Rec_1695459,Human_Splice_Rec_1695497,Human_Splice_Rec_1695551,Human_Splice_Rec_1695583,Human_Splice_Rec_1695619,Human_Splice_Rec_1695661,Human_Splice_Rec_1695717,Human_Splice_Rec_1695733,Human_Splice_Rec_1695803,Human_Splice_Rec_1695829,Human_Splice_Rec_1695857,Human_Splice_Rec_1695871,Human_Splice_Rec_1695901,Human_Splice_Rec_1695923,Human_Splice_Rec_1695949,Human_Splice_Rec_1695981,Human_Splice_Rec_1696003,Human_Splice_Rec_1696031,Human_Splice_Rec_1696101,Human_Splice_Rec_1696127,Human_Splice_Rec_1696169,Human_Splice_Rec_1696201,Human_Splice_Rec_1696225,Human_Splice_Rec_1696247,Human_Splice_Rec_1696271,Human_Splice_Rec_1696291,Human_Splice_Rec_1696331,Human_Splice_Rec_1696357,Human_Splice_Rec_1696387,Human_Splice_Rec_1696413,Human_Splice_Rec_1696437,Human_Splice_Rec_1696619,Human_Splice_Rec_1696645,Human_Splice_Rec_1696699,Human_Splice_Rec_1696729,Human_Splice_Rec_1696755,Human_Splice_Rec_1696791,Human_Splice_Rec_1696823,Human_Splice_Rec_1696873,Human_Splice_Rec_1696889 Human_miRNA_ID_2222877,Human_miRNA_ID_2441999,Human_miRNA_ID_2485937,Human_miRNA_ID_3074309 RMVar_hsa_circ_7746,RMVar_hsa_circ_86047,RMVar_hsa_circ_96211,RMVar_hsa_circ_102061,RMVar_hsa_circ_93307,RMVar_hsa_circ_177635,RMVar_hsa_circ_177637,RMVar_hsa_circ_177639,RMVar_hsa_circ_77515,RMVar_hsa_circ_177638,RMVar_hsa_circ_177636,RMVar_hsa_circ_177640,RMVar_hsa_circ_106815,RMVar_hsa_circ_22199,RMVar_hsa_circ_12256,RMVar_hsa_circ_33899,RMVar_hsa_circ_110227,RMVar_hsa_circ_177641,RMVar_hsa_circ_177642,RMVar_hsa_circ_318299,RMVar_hsa_circ_317493,RMVar_hsa_circ_177643,RMVar_hsa_circ_67331,RMVar_hsa_circ_177644 66347 RMVar_ID_66347 Human_SNP_ID_599015677 m1A Human chr16 + 28487699 28487699 28487699 GGGCAGCAGGTGAAGGCCAAGAGGAGCCAACAATTTGATGACGAGTGTGGGGAGGATGTCCGCCA GGGCAGCAGGTGAAGGCCAAGAGGAGCCAACAGTTTGATGACGAGTGTGGGGAGGATGTCCGCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28486643..28487718 26863196 MeRIP-seq:(Medium) rs745665200 Functional Loss SNV dbSNP153 33..33 33 - - - 66348 RMVar_ID_66348 Human_SNP_ID_599016835 m1A Human chr16 + 28491524 28491524 28491524 CCGCGTTCTTCCAATGCGCGCCCTGATGGTCCAACAGAGGGAGCCGGGGCTCCGGGACGGTCTCC CCGCGTTCTTCCAATGCGCGCCCTGATGGTCCGACAGAGGGAGCCGGGGCTCCGGGACGGTCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28491488..28492025 26863196 MeRIP-seq:(Medium) rs1040287399 Functional Loss SNV dbSNP153 33..33 33 - - - 66349 RMVar_ID_66349 Human_SNP_ID_599018031 m1A Human chr16 + 28495544 28495544 28495544 GGAGAGGCAGGAGTCCCATGAGCAGGAAGTGAACAGAGAAGAGAGGCTGAGAAGCTGGGAACAGG GGAGAGGCAGGAGTCCCATGAGCAGGAAGTGAGCAGAGAAGAGAGGCTGAGAAGCTGGGAACAGG A G APOBR Ensembl:ENSG00000184730 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28495495..28495660 26863196 MeRIP-seq:(Medium) rs1342407786 Functional Loss SNV dbSNP153 33..33 33 - - - 66350 RMVar_ID_66350 Human_SNP_ID_599018746 m1A Human chr16 - 28496911 28496911 28496911 TCTCTCCATGTCCTTTCTCGTGCGGTTTTCCCAGGCTCCTGGGAAGGCCTCGGAGGCCTCAGGCT TCTCTCCATGTCCTTTCTCGTGCGGTTTTCCCGGGCTCCTGGGAAGGCCTCGGAGGCCTCAGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28496854..28497162 26863196 MeRIP-seq:(Medium) rs1395026644 Functional Loss SNV dbSNP153 33..33 33 - - - 66351 RMVar_ID_66351 Human_SNP_ID_599029408 m1A Human chr16 - 28535683 28535678 28535683 GAAAGAGAAAAAGAAGGAAGGAAGGAAAAGAAAGGAAGGAAGAAAGAAAAGAAAGAGAGAAAGGA GAAAGAGAAAAAGAAGGAAGGAAGGAAAAGAA_____GGAAGAAAGAAAAGAAAGAGAGAAAGGA CTTCCT C NUPR1 Ensembl:ENSG00000176046 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28535632..28535716 26863196 MeRIP-seq:(Medium) rs1469561606 Functional Loss DEL dbSNP153 33..37 33 - - - 66352 RMVar_ID_66352 Human_SNP_ID_599029411 m1A Human chr16 - 28535683 28535683 28535683 GAAAGAGAAAAAGAAGGAAGGAAGGAAAAGAAAGGAAGGAAGAAAGAAAAGAAAGAGAGAAAGGA GAAAGAGAAAAAGAAGGAAGGAAGGAAAAGAAGGGAAGGAAGAAAGAAAAGAAAGAGAGAAAGGA T C NUPR1 Ensembl:ENSG00000176046 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28535632..28535716 26863196 MeRIP-seq:(Medium) rs867976952 Functional Loss SNV dbSNP153 33..33 33 - - - 66353 RMVar_ID_66353 Human_SNP_ID_599029983 m1A Human chr16 - 28538038 28538038 28538038 GGTGACCAAGCTGCAGAATTCAGAGAGGAAGAAGCGAGGGGCACGGCGCTGAGACAGAGCTGGAG GGTGACCAAGCTGCAGAATTCAGAGAGGAAGACGCGAGGGGCACGGCGCTGAGACAGAGCTGGAG T G NUPR1 Ensembl:ENSG00000176046 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28537419..28538585 26863196 MeRIP-seq:(Medium) rs1347283568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1696995,Human_Splice_Rec_1697001,Human_Splice_Rec_1697005 RMVar_hsa_circ_58752,RMVar_hsa_circ_83275,RMVar_hsa_circ_177650 66354 RMVar_ID_66354 Human_SNP_ID_599034251 m1A Human chr16 + 28553996 28553996 28553996 CGGTTCTCGACGTGCCGCCAATCTTCGAACGCAGGTCTGTGATCATCCGCAGACTCCGAAAAAGG CGGTTCTCGACGTGCCGCCAATCTTCGAACGCGGGTCTGTGATCATCCGCAGACTCCGAAAAAGG A G SGF29 Ensembl:ENSG00000176476 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28553947..28581119 26863196 MeRIP-seq:(Medium) rs1322954150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515855,Human_RBP_ID_4393690 66355 RMVar_ID_66355 Human_SNP_ID_599054173 m1A Human chr16 - 28623519 28623519 28623519 AGGCCCGGAGGCGGTGCAGGAAGCCTCCGACCACGCGGGCTCCTGATCGCGGGCGCCCACAGCGC AGGCCCGGAGGCGGTGCAGGAAGCCTCCGACCTCGCGGGCTCCTGATCGCGGGCGCCCACAGCGC T A SULT1A1 Ensembl:ENSG00000196502 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:28623468..28623594;chr16:28623478..28623563 26863196 MeRIP-seq:(Medium) rs1567321450 Functional Loss SNV dbSNP153 33..33 33 - - - 66356 RMVar_ID_66356 Human_SNP_ID_599054176 m1A Human chr16 + 28623526 28623526 28623526 GGGCGCCCGCGATCAGGAGCCCGCGTGGTCGGAGGCTTCCTGCACCGCCTCCGGGCCTCGCCAGC GGGCGCCCGCGATCAGGAGCCCGCGTGGTCGGGGGCTTCCTGCACCGCCTCCGGGCCTCGCCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28623478..28623549 26863196 MeRIP-seq:(Medium) rs1000935596 Functional Loss SNV dbSNP153 33..33 33 - - - 66357 RMVar_ID_66357 Human_SNP_ID_599072411 m1A Human chr16 + 28723256 28723256 28723256 GAAGAAGCACGACAGGAAATCCAAGCGCCTGGATGAGGAGGAGGAGGACAATGAAGGCGGGGAGT GAAGAAGCACGACAGGAAATCCAAGCGCCTGGTTGAGGAGGAGGAGGACAATGAAGGCGGGGAGT A T EIF3C Ensembl:ENSG00000184110 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:28723162..28723365 26863196 MeRIP-seq:(Medium) rs759652982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45667,Human_RBP_ID_762122,Human_RBP_ID_817345,Human_RBP_ID_894084,Human_RBP_ID_4398179,Human_RBP_ID_5576713,Human_RBP_ID_6506133,Human_RBP_ID_9372576,Human_RBP_ID_12711999,Human_RBP_ID_17669664,Human_RBP_ID_22945647,Human_RBP_ID_24544401,Human_RBP_ID_24551911,Human_RBP_ID_26328843,Human_RBP_ID_26941921,Human_RBP_ID_27811013 Human_Splice_Rec_1697316,Human_Splice_Rec_1697317,Human_Splice_Rec_1697356,Human_Splice_Rec_1697357,Human_Splice_Rec_1697404,Human_Splice_Rec_1697405,Human_Splice_Rec_1697444,Human_Splice_Rec_1697445,Human_Splice_Rec_1697482,Human_Splice_Rec_1697483,Human_Splice_Rec_1697523 Human_miRNA_ID_2255366 RMVar_hsa_circ_99307,RMVar_hsa_circ_177656,RMVar_hsa_circ_121454,RMVar_hsa_circ_177657,RMVar_hsa_circ_127191,RMVar_hsa_circ_91480,RMVar_hsa_circ_177659,RMVar_hsa_circ_339844,RMVar_hsa_circ_177661,RMVar_hsa_circ_62207,RMVar_hsa_circ_177660 66358 RMVar_ID_66358 Human_SNP_ID_599072412 m1A Human chr16 + 28723259 28723257 28723260 GAAGCACGACAGGAAATCCAAGCGCCTGGATGAGGAGGAGGAGGACAATGAAGGCGGGGAGTGGG GAAGCACGACAGGAAATCCAAGCGCCTGGAT___GAGGAGGAGGACAATGAAGGCGGGGAGTGGG TGAG T EIF3C Ensembl:ENSG00000184110 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:28723201..28723325 26863196 MeRIP-seq:(Medium) rs772308295 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_45667,Human_RBP_ID_762122,Human_RBP_ID_817345,Human_RBP_ID_894084,Human_RBP_ID_4398179,Human_RBP_ID_5576713,Human_RBP_ID_6506133,Human_RBP_ID_9372576,Human_RBP_ID_12711999,Human_RBP_ID_17669664,Human_RBP_ID_22945647,Human_RBP_ID_24544401,Human_RBP_ID_24551911,Human_RBP_ID_26328843,Human_RBP_ID_26941921,Human_RBP_ID_27811013 Human_Splice_Rec_1697316,Human_Splice_Rec_1697317,Human_Splice_Rec_1697356,Human_Splice_Rec_1697357,Human_Splice_Rec_1697404,Human_Splice_Rec_1697405,Human_Splice_Rec_1697444,Human_Splice_Rec_1697445,Human_Splice_Rec_1697482,Human_Splice_Rec_1697483,Human_Splice_Rec_1697523 Human_miRNA_ID_2195908,Human_miRNA_ID_2255366 RMVar_hsa_circ_99307,RMVar_hsa_circ_177656,RMVar_hsa_circ_121454,RMVar_hsa_circ_177657,RMVar_hsa_circ_127191,RMVar_hsa_circ_91480,RMVar_hsa_circ_177659,RMVar_hsa_circ_339844,RMVar_hsa_circ_177661,RMVar_hsa_circ_62207,RMVar_hsa_circ_177660 66359 RMVar_ID_66359 Human_SNP_ID_599072413 m1A Human chr16 - 28723257 28723257 28723257 CACTCCCCGCCTTCATTGTCCTCCTCCTCCTCATCCAGGCGCTTGGATTTCCTGTCGTGCTTCTT CACTCCCCGCCTTCATTGTCCTCCTCCTCCTCGTCCAGGCGCTTGGATTTCCTGTCGTGCTTCTT T C AC145285.4 Ensembl:ENSG00000261419 Pseudogene intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:28723176..28723411 26863196 MeRIP-seq:(Medium) rs1417013731 Functional Loss SNV dbSNP153 33..33 33 - - - 66360 RMVar_ID_66360 Human_SNP_ID_599072422 m1A Human chr16 - 28723275 28723275 28723275 CCGCCCCGGACCCTTTCCCACTCCCCGCCTTCATTGTCCTCCTCCTCCTCATCCAGGCGCTTGGA CCGCCCCGGACCCTTTCCCACTCCCCGCCTTCGTTGTCCTCCTCCTCCTCATCCAGGCGCTTGGA T C AC145285.4 Ensembl:ENSG00000261419 Pseudogene intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:28723255..28723479 26863410 MeRIP-seq:(Medium) rs370969548 Functional Loss SNV dbSNP153 33..33 33 - - - 66361 RMVar_ID_66361 Human_SNP_ID_599091822 m1A Human chr16 + 28822630 28822628 28822630 GCGGAAGAGCCTCACGCACGACGTGCCGCCTCACACTCCCGCGGAGGCATCGCGACGCAGCGACG GCGGAAGAGCCTCACGCACGACGTGCCGCCT__CACTCCCGCGGAGGCATCGCGACGCAGCGACG TCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28822579..28822828 32194978 MeRIP-seq:(Medium) rs1248269947 Functional Loss DEL dbSNP153 32..33 33 - - - 66362 RMVar_ID_66362 Human_SNP_ID_599092034 m1A Human chr16 + 28822963 28822959 28822963 CCTGGCCCCCCCCCCCCCCCCCCCCCCCCGGGAGCTCCCACCCGCGCGCTCCTCCCTCTCCGCTC CCTGGCCCCCCCCCCCCCCCCCCCCCCCC____GCTCCCACCCGCGCGCTCCTCCCTCTCCGCTC CGGGA C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:28822777..28823350;chr16:28822845..28823275;chr16:28822808..28823300 26863196 MeRIP-seq:(Medium) rs1309358961 Functional Loss DEL dbSNP153 30..33 33 - - - 66363 RMVar_ID_66363 Human_SNP_ID_599092189 m1A Human chr16 - 28823217 28823213 28823217 TCCGGAAGGGGAATTAGAGAGAAGGGAGGGAGAGAGGGGGCCGGGGCTGGGGCCCCGCTGGAGAG TCCGGAAGGGGAATTAGAGAGAAGGGAGGGAG____GGGGCCGGGGCTGGGGCCCCGCTGGAGAG CCTCT C AC145285.6 Ensembl:ENSG00000275807 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28822737..28823607 26863196 MeRIP-seq:(Medium) rs758300889 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8184469,Human_RBP_ID_17067821 66364 RMVar_ID_66364 Human_SNP_ID_599092190 m1A Human chr16 - 28823217 28823213 28823217 TCCGGAAGGGGAATTAGAGAGAAGGGAGGGAGAGAGGGGGCCGGGGCTGGGGCCCCGCTGGAGAG TCCGGAAGGGGAATTAGAGAGAAGGGAGGGAG__AGGGGGCCGGGGCTGGGGCCCCGCTGGAGAG CCTCT CCT AC145285.6 Ensembl:ENSG00000275807 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28822737..28823607 26863196 MeRIP-seq:(Medium) rs758300889 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8184469,Human_RBP_ID_17067821 66365 RMVar_ID_66365 Human_SNP_ID_599092289 m1A Human chr16 - 28823358 28823358 28823358 GTGGCCAGCGGCCCCGGGAGGCCGCCGTTGGGAGGGCTGGTGCCCCCGGGGGGCCGACGGGCCAC GTGGCCAGCGGCCCCGGGAGGCCGCCGTTGGGCGGGCTGGTGCCCCCGGGGGGCCGACGGGCCAC T G AC145285.6 Ensembl:ENSG00000275807 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28823351..28823375 26863196 MeRIP-seq:(Medium) rs775446640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261468,Human_RBP_ID_3504443 66366 RMVar_ID_66366 Human_SNP_ID_599092469 m1A Human chr16 + 28823793 28823793 28823793 CGCTCGGCTCTCGGGGCCTAGTCAGGGCTCGCAGCCCCGGCCTTCAGGGGAGGCGGGGCGCATCC CGCTCGGCTCTCGGGGCCTAGTCAGGGCTCGCGGCCCCGGCCTTCAGGGGAGGCGGGGCGCATCC A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28823792..28823891 26863196 MeRIP-seq:(Medium) rs1314554197 Functional Loss SNV dbSNP153 33..33 33 - - - 66367 RMVar_ID_66367 Human_SNP_ID_599092741 m1A Human chr16 + 28824410 28824410 28824410 GTGGGTTTTAGTGCGCAGGCGCAGACCGGGCGAGGCCTCCCGGTGGATGGCTTTTGCGGCTGCGC GTGGGTTTTAGTGCGCAGGCGCAGACCGGGCGCGGCCTCCCGGTGGATGGCTTTTGCGGCTGCGC A C ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28824408..28824617 32194978 MeRIP-seq:(Medium) rs1364076065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502659 66368 RMVar_ID_66368 Human_SNP_ID_599094663 m1A Human chr16 + 28829977 28829977 28829977 CCAGTACCGCCTACGGATCGCCATGGAGAACGACGATGGGCGCACTGAAGAGGAGAAGCACAGTG CCAGTACCGCCTACGGATCGCCATGGAGAACGGCGATGGGCGCACTGAAGAGGAGAAGCACAGTG A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28829927..28829999 26863196 MeRIP-seq:(Medium) rs1466515495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895745,Human_RBP_ID_1003807,Human_RBP_ID_1515912,Human_RBP_ID_1840971,Human_RBP_ID_3949032,Human_RBP_ID_4360785,Human_RBP_ID_5576714,Human_RBP_ID_6506216,Human_RBP_ID_9372578,Human_RBP_ID_17253781,Human_RBP_ID_18529734,Human_RBP_ID_18676877,Human_RBP_ID_18983524,Human_RBP_ID_22497580,Human_RBP_ID_22532777 Human_Splice_Rec_1697609,Human_Splice_Rec_1697649,Human_Splice_Rec_1697693,Human_Splice_Rec_1697737,Human_Splice_Rec_1697783,Human_Splice_Rec_1697825,Human_Splice_Rec_1697869,Human_Splice_Rec_1697913,Human_Splice_Rec_1697965,Human_Splice_Rec_1697989,Human_Splice_Rec_1698013,Human_Splice_Rec_1698019 RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_51683,RMVar_hsa_circ_49675,RMVar_hsa_circ_308413,RMVar_hsa_circ_357091,RMVar_hsa_circ_177671 66369 RMVar_ID_66369 Human_SNP_ID_599094958 m1A Human chr16 - 28830804 28830804 28830804 GCATCCCCTTCCCTGCCCTCTTCCTCAAAGTCACCTCATAACTCACCTCCATTGATACCACGGGC GCATCCCCTTCCCTGCCCTCTTCCTCAAAGTCGCCTCATAACTCACCTCCATTGATACCACGGGC T C AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28830801..28830944 26863196 MeRIP-seq:(Medium) rs1234648230 Functional Loss SNV dbSNP153 33..33 33 - - - 66370 RMVar_ID_66370 Human_SNP_ID_599095445 m1A Human chr16 + 28832213 28832213 28832213 CTACAGCTCCCCCTTTTCTTCCAGTGGGCCGGATGTATCCCCCGCGTTCTCCCAAGTCTGCTGCC CTACAGCTCCCCCTTTTCTTCCAGTGGGCCGGCTGTATCCCCCGCGTTCTCCCAAGTCTGCTGCC A C ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28832201..28832325 26863196 MeRIP-seq:(Medium) rs1276286269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895584,Human_RBP_ID_17874759,Human_RBP_ID_18676884,Human_RBP_ID_22532779,Human_RBP_ID_22800720,Human_RBP_ID_22937932,Human_RBP_ID_25243623,Human_RBP_ID_26941951 Human_Splice_Rec_1697614,Human_Splice_Rec_1697654,Human_Splice_Rec_1697698,Human_Splice_Rec_1697742,Human_Splice_Rec_1697788,Human_Splice_Rec_1697830,Human_Splice_Rec_1697874,Human_Splice_Rec_1697918,Human_Splice_Rec_1698018 Human_miRNA_ID_2653486 RMVar_hsa_circ_4350,RMVar_hsa_circ_369517,RMVar_hsa_circ_177670,RMVar_hsa_circ_4213,RMVar_hsa_circ_49675 66371 RMVar_ID_66371 Human_SNP_ID_599095782 m1A Human chr16 - 28833099 28833099 28833099 CTTTGGGCTCCTCCTTTAAGATCCGGGGAGGAAAAGGATCCAGGCTGTTCTCAGGGGAGCTACTG CTTTGGGCTCCTCCTTTAAGATCCGGGGAGGAGAAGGATCCAGGCTGTTCTCAGGGGAGCTACTG T C AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28830951..28833138 32194978 MeRIP-seq:(Medium) rs1487144703 Functional Loss SNV dbSNP153 33..33 33 - - - 66372 RMVar_ID_66372 Human_SNP_ID_599095855 m1A Human chr16 + 28833286 28833286 28833286 GAGGGGCCAGAGCAGCCCCCACCACCTTGTCCAAGCCAAACTGGCAGCCCCCCGGTGGGCCTCAT GAGGGGCCAGAGCAGCCCCCACCACCTTGTCCGAGCCAAACTGGCAGCCCCCCGGTGGGCCTCAT A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28833236..28833393 26863196 MeRIP-seq:(Medium) rs764115092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45388,Human_RBP_ID_1365422,Human_RBP_ID_4360828,Human_RBP_ID_17253788,Human_RBP_ID_22800730,Human_RBP_ID_27441002,Human_RBP_ID_27811015 Human_Splice_Rec_1697621,Human_Splice_Rec_1697661,Human_Splice_Rec_1697705,Human_Splice_Rec_1697749,Human_Splice_Rec_1697795,Human_Splice_Rec_1697837,Human_Splice_Rec_1697881,Human_Splice_Rec_1697925,Human_Splice_Rec_1697995,Human_Splice_Rec_1698021 RMVar_hsa_circ_49675,RMVar_hsa_circ_88072,RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_177673 66373 RMVar_ID_66373 Human_SNP_ID_599096141 m1A Human chr16 + 28834165 28834165 28834165 GACAGCAGGCCAGAGTGGGCTATACAGCCCCCAGTACATCTCCTACATACCTCAGATCCACATGG GACAGCAGGCCAGAGTGGGCTATACAGCCCCCGGTACATCTCCTACATACCTCAGATCCACATGG A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28834114..28834620 32194978 MeRIP-seq:(Medium) rs1279131377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1840989,Human_RBP_ID_3493880,Human_RBP_ID_3947520,Human_RBP_ID_9372583,Human_RBP_ID_17253791,Human_RBP_ID_17369414,Human_RBP_ID_17485971,Human_RBP_ID_17874765,Human_RBP_ID_24476007,Human_RBP_ID_26941969,Human_RBP_ID_27239876 Human_Splice_Rec_1697625,Human_Splice_Rec_1697665,Human_Splice_Rec_1697709,Human_Splice_Rec_1697753,Human_Splice_Rec_1697799,Human_Splice_Rec_1697841,Human_Splice_Rec_1697885,Human_Splice_Rec_1697929,Human_Splice_Rec_1697999,Human_Splice_Rec_1698025,Human_Splice_Rec_1698031,Human_Splice_Rec_1698039,Human_Splice_Rec_1698051 RMVar_hsa_circ_49675,RMVar_hsa_circ_88072,RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_177673 66374 RMVar_ID_66374 Human_SNP_ID_599096277 m1A Human chr16 - 28834449 28834449 28834449 GCTCAAGCTCCACCTGCCAGTAGGCCCTTGGCAGCCTCGCCGCCTGCCCCTCCCAGCCCTGCTCA GCTCAAGCTCCACCTGCCAGTAGGCCCTTGGCCGCCTCGCCGCCTGCCCCTCCCAGCCCTGCTCA T G AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:28834445..28834625 26863196 MeRIP-seq:(Medium) rs1353278937 Functional Loss SNV dbSNP153 33..33 33 - - - 66375 RMVar_ID_66375 Human_SNP_ID_599096389 m1A Human chr16 + 28834690 28834690 28834690 GCCATGATGCAGCCCATGGCCCACTACCCCTCACAGGTGACTGCGGCCCAGGAGGGCAGTGAGGA GCCATGATGCAGCCCATGGCCCACTACCCCTCGCAGGTGACTGCGGCCCAGGAGGGCAGTGAGGA A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:28834539..28834741 26863196 MeRIP-seq:(Medium) rs138550733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234101,Human_RBP_ID_17256008,Human_RBP_ID_17369419,Human_RBP_ID_17488241,Human_RBP_ID_17874768,Human_RBP_ID_18940127,Human_RBP_ID_19071232 Human_Splice_Rec_1697629,Human_Splice_Rec_1697669,Human_Splice_Rec_1697713,Human_Splice_Rec_1697757,Human_Splice_Rec_1697803,Human_Splice_Rec_1697845,Human_Splice_Rec_1697889,Human_Splice_Rec_1697933,Human_Splice_Rec_1698003,Human_Splice_Rec_1698029,Human_Splice_Rec_1698035,Human_Splice_Rec_1698043,Human_Splice_Rec_1698055,Human_Splice_Rec_1698067 Human_miRNA_ID_464661,Human_miRNA_ID_874309,Human_miRNA_ID_1232682,Human_miRNA_ID_1559934,Human_miRNA_ID_2153639,Human_miRNA_ID_2801516,Human_miRNA_ID_3009649 RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_45278 66376 RMVar_ID_66376 Human_SNP_ID_599096547 m1A Human chr16 - 28835125 28835125 28835125 CAGAAGGGTACTGAGGGGTAGAGGATGACACGATGGCCTGGGGATGGCTGCCCGACGTCAGCATG CAGAAGGGTACTGAGGGGTAGAGGATGACACGCTGGCCTGGGGATGGCTGCCCGACGTCAGCATG T G AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28835101..28835200 26863196 MeRIP-seq:(Medium) rs370559547 Functional Loss SNV dbSNP153 33..33 33 - - - 66377 RMVar_ID_66377 Human_SNP_ID_599096562 m1A Human chr16 + 28835161 28835161 28835161 GTCATCCTCTACCCCTCAGTACCCTTCTGCAGAGCAGCCTACCCCCCAAGCCCTTTATGGTGAGT GTCATCCTCTACCCCTCAGTACCCTTCTGCAGGGCAGCCTACCCCCCAAGCCCTTTATGGTGAGT A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:28835051..28835200;chr16:28835047..28835325 26863196 MeRIP-seq:(Medium) rs746599125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45395,Human_RBP_ID_234102,Human_RBP_ID_6506255,Human_RBP_ID_17077885,Human_RBP_ID_17256011,Human_RBP_ID_17371370,Human_RBP_ID_18938957,Human_RBP_ID_23685645 Human_Splice_Rec_1697631,Human_Splice_Rec_1697671,Human_Splice_Rec_1697715,Human_Splice_Rec_1697759,Human_Splice_Rec_1697805,Human_Splice_Rec_1697847,Human_Splice_Rec_1697891,Human_Splice_Rec_1697935,Human_Splice_Rec_1698005,Human_Splice_Rec_1698037,Human_Splice_Rec_1698045,Human_Splice_Rec_1698057,Human_Splice_Rec_1698069,Human_Splice_Rec_1698071 Human_miRNA_ID_1751891,Human_miRNA_ID_1767919,Human_miRNA_ID_2395882,Human_miRNA_ID_2908236,Human_miRNA_ID_3027075 RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_25635,RMVar_hsa_circ_373851,RMVar_hsa_circ_177675 66378 RMVar_ID_66378 Human_SNP_ID_599096621 m1A Human chr16 + 28835280 28835280 28835280 AGCACTGGTTCTCCCTCTTTCCTGCTGCAGCCACTGTTCACCAGTCCTACCCACACCATGCCACA AGCACTGGTTCTCCCTCTTTCCTGCTGCAGCCGCTGTTCACCAGTCCTACCCACACCATGCCACA A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28835274..28835340 26863196 MeRIP-seq:(Medium) rs776934100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234103,Human_RBP_ID_471782,Human_RBP_ID_761929,Human_RBP_ID_2472682,Human_RBP_ID_5113876,Human_RBP_ID_5128563,Human_RBP_ID_17077445,Human_RBP_ID_17253799,Human_RBP_ID_17371373,Human_RBP_ID_17488399,Human_RBP_ID_18940131,Human_RBP_ID_26440515,Human_RBP_ID_26941978,Human_RBP_ID_27239880 Human_Splice_Rec_1697632,Human_Splice_Rec_1697672,Human_Splice_Rec_1697716,Human_Splice_Rec_1697760,Human_Splice_Rec_1697806,Human_Splice_Rec_1697848,Human_Splice_Rec_1697892,Human_Splice_Rec_1697936,Human_Splice_Rec_1698006,Human_Splice_Rec_1698038,Human_Splice_Rec_1698046,Human_Splice_Rec_1698058,Human_Splice_Rec_1698070,Human_Splice_Rec_1698072 RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_25635,RMVar_hsa_circ_7744 66379 RMVar_ID_66379 Human_SNP_ID_599096783 m1A Human chr16 - 28835678 28835678 28835678 GTGGATGGCATACACAGCGGCTGGCTGGGGGAAGCTGCTCTGAGGGGACTGGGCAGAAGGTCCCG GTGGATGGCATACACAGCGGCTGGCTGGGGGAGGCTGCTCTGAGGGGACTGGGCAGAAGGTCCCG T C AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28835627..28835709 26863196 MeRIP-seq:(Medium) rs1233204243 Functional Loss SNV dbSNP153 33..33 33 - - - 66380 RMVar_ID_66380 Human_SNP_ID_599096921 m1A Human chr16 + 28836042 28836042 28836042 GCACCCACCCCAGAGTCATGGGGGGCCCCCCCAAGGCGCGGTGCCCCAGAGTGGGGTGCCTGCAC GCACCCACCCCAGAGTCATGGGGGGCCCCCCCTAGGCGCGGTGCCCCAGAGTGGGGTGCCTGCAC A T ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28836007..28836084 26863196 MeRIP-seq:(Medium) rs1408632862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46305,Human_RBP_ID_471785,Human_RBP_ID_4398230,Human_RBP_ID_5114411,Human_RBP_ID_5128091,Human_RBP_ID_17078174,Human_RBP_ID_17371382,Human_RBP_ID_17690003,Human_RBP_ID_18189905,Human_RBP_ID_26941986 Human_Splice_Rec_1697677,Human_Splice_Rec_1697853,Human_Splice_Rec_1698079,Human_Splice_Rec_1698085 66381 RMVar_ID_66381 Human_SNP_ID_599097030 m1A Human chr16 - 28836309 28836309 28836309 CTGCCCACCCTACATACTTCACAGACAGGTGCAGGTCGGCGGGCGCCCTGTGGGACAGCCCTGCC CTGCCCACCCTACATACTTCACAGACAGGTGCGGGTCGGCGGGCGCCCTGTGGGACAGCCCTGCC T C AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28836168..28836425 26863196 MeRIP-seq:(Medium) rs756041540 Functional Loss SNV dbSNP153 33..33 33 - - - 66382 RMVar_ID_66382 Human_SNP_ID_599097043 m1A Human chr16 - 28836351 28836351 28836351 ACAGAGCCAGGAGCAAGCCCCTGGCGGCGGCGACTGTGGCTTCTGCCCACCCTACATACTTCACA ACAGAGCCAGGAGCAAGCCCCTGGCGGCGGCGTCTGTGGCTTCTGCCCACCCTACATACTTCACA T A AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28836155..28836500 26863196 MeRIP-seq:(Medium) rs1253869658 Functional Loss SNV dbSNP153 33..33 33 - - - 66383 RMVar_ID_66383 Human_SNP_ID_599097059 m1A Human chr16 - 28836368 28836368 28836368 ACGGAGGGAAGCAAAGGACAGAGCCAGGAGCAAGCCCCTGGCGGCGGCGACTGTGGCTTCTGCCC ACGGAGGGAAGCAAAGGACAGAGCCAGGAGCACGCCCCTGGCGGCGGCGACTGTGGCTTCTGCCC T G AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:28836251..28836641 26863410 MeRIP-seq:(Medium) rs766716534 Functional Loss SNV dbSNP153 33..33 33 - - - 66384 RMVar_ID_66384 Human_SNP_ID_599097356 m1A Human chr16 + 28837057 28837057 28837057 TCTATTCCCCCGCTGGAGACGGAAGATCTTTTATTTTCTATTATTTATAACTTCAGACTTGGGCC TCTATTCCCCCGCTGGAGACGGAAGATCTTTTGTTTTCTATTATTTATAACTTCAGACTTGGGCC A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28837007..28837108 26863196 MeRIP-seq:(Medium) rs1465822333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471799,Human_RBP_ID_1840999,Human_RBP_ID_5141862,Human_RBP_ID_6506277,Human_RBP_ID_17078180,Human_RBP_ID_17253807,Human_RBP_ID_17485989,Human_RBP_ID_18163526,Human_RBP_ID_18529736,Human_RBP_ID_20168590,Human_RBP_ID_23685654,Human_RBP_ID_24413087,Human_RBP_ID_24476019,Human_RBP_ID_26444987,Human_RBP_ID_27441014 66385 RMVar_ID_66385 Human_SNP_ID_599099260 m1A Human chr16 + 28843071 28843071 28843071 CCAATAGTCCGGTTGCCATCTCGCAGGGTGAAACGCTGGCCTTTCTCTAAGATCATTGGCTGCCG CCAATAGTCCGGTTGCCATCTCGCAGGGTGAACCGCTGGCCTTTCTCTAAGATCATTGGCTGCCG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:28842801..28843150 32194978 MeRIP-seq:(Medium) rs1342548394 Functional Loss SNV dbSNP153 33..33 33 - - - 66386 RMVar_ID_66386 Human_SNP_ID_599099265 m1A Human chr16 + 28843087 28843087 28843087 CATCTCGCAGGGTGAAACGCTGGCCTTTCTCTAAGATCATTGGCTGCCGCAAGATTAGGTTGAAC CATCTCGCAGGGTGAAACGCTGGCCTTTCTCTGAGATCATTGGCTGCCGCAAGATTAGGTTGAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28842875..28843092 26863196 MeRIP-seq:(Medium) rs746833692 Functional Loss SNV dbSNP153 33..33 33 - - - 66387 RMVar_ID_66387 Human_SNP_ID_599099275 m1A Human chr16 + 28843108 28843108 28843108 GGCCTTTCTCTAAGATCATTGGCTGCCGCAAGATTAGGTTGAACTTCAGGTCCTCCCCGGGCATG GGCCTTTCTCTAAGATCATTGGCTGCCGCAAGGTTAGGTTGAACTTCAGGTCCTCCCCGGGCATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28842878..28843169 26863196 MeRIP-seq:(Medium) rs1406451993 Functional Loss SNV dbSNP153 33..33 33 - - - 66388 RMVar_ID_66388 Human_SNP_ID_599099440 m1A Human chr16 - 28843706 28843706 28843706 AAGGTACGGTGGGTGGGAGGAATGTAGGGTGGAGGGGGGACTTTTTATATTACCTTTGCTTCACT AAGGTACGGTGGGTGGGAGGAATGTAGGGTGGCGGGGGGACTTTTTATATTACCTTTGCTTCACT T G TUFM Ensembl:ENSG00000178952 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28843705..28843834 26863196 MeRIP-seq:(Medium) rs902591990 Functional Loss SNV dbSNP153 33..33 33 - - - 66389 RMVar_ID_66389 Human_SNP_ID_599099879 m1A Human chr16 + 28844860 28844860 28844860 TTGTTCACATACACCACCACATGCTCCACCCCAATCTGTAGATGCCAGAGAGACAGGGACAATAT TTGTTCACATACACCACCACATGCTCCACCCCCATCTGTAGATGCCAGAGAGACAGGGACAATAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr16:28844669..28845095;chr16:28844845..28845075 26863196 MeRIP-seq:(Medium) rs1339000349 Functional Loss SNV dbSNP153 33..33 33 - - - 66390 RMVar_ID_66390 Human_SNP_ID_599099880 m1A Human chr16 + 28844860 28844860 28844860 TTGTTCACATACACCACCACATGCTCCACCCCAATCTGTAGATGCCAGAGAGACAGGGACAATAT TTGTTCACATACACCACCACATGCTCCACCCCGATCTGTAGATGCCAGAGAGACAGGGACAATAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr16:28844669..28845095;chr16:28844845..28845075 26863196 MeRIP-seq:(Medium) rs1339000349 Functional Loss SNV dbSNP153 33..33 33 - - - 66391 RMVar_ID_66391 Human_SNP_ID_599099945 m1A Human chr16 + 28844988 28844988 28844988 TGGCCAGTAATAAGTGCTCTCGGGTCTGGGGCATGGGGCCGTCATTGGCTGCTACCACCAGGATG TGGCCAGTAATAAGTGCTCTCGGGTCTGGGGCGTGGGGCCGTCATTGGCTGCTACCACCAGGATG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28844976..28845025 26863196 MeRIP-seq:(Medium) rs781744069 Functional Loss SNV dbSNP153 33..33 33 - - - 66392 RMVar_ID_66392 Human_SNP_ID_599099973 m1A Human chr16 - 28845057 28845057 28845057 GAACTTGGCTGTTTCCTTTCCTTCTCCTCTCCAGAATATGATCACAGGCACTGCACCCCTCGACG GAACTTGGCTGTTTCCTTTCCTTCTCCTCTCCGGAATATGATCACAGGCACTGCACCCCTCGACG T C TUFM Ensembl:ENSG00000178952 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28844934..28845075 26863196 MeRIP-seq:(Medium) rs1477272184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45635,Human_RBP_ID_20111364,Human_RBP_ID_24476024,Human_RBP_ID_26942036,Human_RBP_ID_27239918 RMVar_hsa_circ_89568,RMVar_hsa_circ_177677 66393 RMVar_ID_66393 Human_SNP_ID_599100050 m1A Human chr16 + 28845305 28845305 28845305 GCAGCTTCTGGCCCTGTCTCCAGTGTCCCAGCAACCCTCACCTTAACATAATCTGCATGACCCGG GCAGCTTCTGGCCCTGTCTCCAGTGTCCCAGCTACCCTCACCTTAACATAATCTGCATGACCCGG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28845301..28846350 26863196 MeRIP-seq:(Medium) rs752788701 Functional Loss SNV dbSNP153 33..33 33 - - - 66394 RMVar_ID_66394 Human_SNP_ID_599100098 m1A Human chr16 + 28845435 28845435 28845435 TACCCCGAGCTCGCTCCTCCGGGGCATTGTCAATCTCCTCGTACTTCTTGAACTTAGCCCCACCT TACCCCGAGCTCGCTCCTCCGGGGCATTGTCAGTCTCCTCGTACTTCTTGAACTTAGCCCCACCT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:28845336..28845502 26863196 MeRIP-seq:(Medium) rs757697518 Functional Loss SNV dbSNP153 33..33 33 - - - 66395 RMVar_ID_66395 Human_SNP_ID_599100104 m1A Human chr16 - 28845450 28845450 28845450 AGTTCTAGCTGAGGGAGGTGGGGCTAAGTTCAAGAAGTACGAGGAGATTGACAATGCCCCGGAGG AGTTCTAGCTGAGGGAGGTGGGGCTAAGTTCAGGAAGTACGAGGAGATTGACAATGCCCCGGAGG T C TUFM Ensembl:ENSG00000178952 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:28845326..28845533 26863196 MeRIP-seq:(Medium) rs779616852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471862,Human_RBP_ID_1365427,Human_RBP_ID_1516021,Human_RBP_ID_1841013,Human_RBP_ID_3949046,Human_RBP_ID_4398274,Human_RBP_ID_9325024,Human_RBP_ID_9372588,Human_RBP_ID_17883783,Human_RBP_ID_22937990,Human_RBP_ID_26942038 Human_Splice_Rec_1698092 RMVar_hsa_circ_89568,RMVar_hsa_circ_177677 66396 RMVar_ID_66396 Human_SNP_ID_599100229 m1A Human chr16 - 28845887 28845886 28845887 CACGAAGAGTGAGTGGGGTTGGGGCGTCCAGCAGCGCCCTATCTACTGATGGGACCTGGAGCCAG CACGAAGAGTGAGTGGGGTTGGGGCGTCCAGC_GCGCCCTATCTACTGATGGGACCTGGAGCCAG CT C TUFM Ensembl:ENSG00000178952 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28845881..28846121 26863196 MeRIP-seq:(Medium) rs1254449259 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5357867,Human_RBP_ID_19071245 66397 RMVar_ID_66397 Human_SNP_ID_599100273 m1A Human chr16 - 28845998 28845998 28845998 CCGCGGCCTGGCCGTGGAGGCCAAGAAGACTTACGTGCGCGACAAGCCACATGTGAATGTGGGTA CCGCGGCCTGGCCGTGGAGGCCAAGAAGACTTGCGTGCGCGACAAGCCACATGTGAATGTGGGTA T C TUFM Ensembl:ENSG00000178952 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28845976..28846325 26863196 MeRIP-seq:(Medium) rs777322797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46351,Human_RBP_ID_471865,Human_RBP_ID_1516027,Human_RBP_ID_4360963,Human_RBP_ID_8811838,Human_RBP_ID_9286226,Human_RBP_ID_9372590,Human_RBP_ID_18207376,Human_RBP_ID_22800772,Human_RBP_ID_26942042,Human_RBP_ID_27239923,Human_RBP_ID_27441033 Human_Splice_Rec_1698091,Human_Splice_Rec_1698113 66398 RMVar_ID_66398 Human_SNP_ID_599100340 m1A Human chr16 + 28846135 28846135 28846135 AGACCTGCCGGGACCGAAGCTTGGAGTCAGGCAGGGAAGGGGTCAGACCGAACCCAGCCACCTAC AGACCTGCCGGGACCGAAGCTTGGAGTCAGGCCGGGAAGGGGTCAGACCGAACCCAGCCACCTAC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:28846133..28846260 26863196 MeRIP-seq:(Medium) rs1421913368 Functional Loss SNV dbSNP153 33..33 33 - - - 66399 RMVar_ID_66399 Human_SNP_ID_599100420 m1A Human chr16 - 28846269 28846269 28846269 GGTCCCGGCTCCCCGGTTACCGGGGCGCGAGTATGACCACAATGGCGGCCGCCACCCTGCTGCGC GGTCCCGGCTCCCCGGTTACCGGGGCGCGAGTGTGACCACAATGGCGGCCGCCACCCTGCTGCGC T C TUFM Ensembl:ENSG00000178952 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28846191..28846350 26863196 MeRIP-seq:(Medium) rs759426337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471870,Human_RBP_ID_4392947,Human_RBP_ID_5495383,Human_RBP_ID_8812326,Human_RBP_ID_9061625,Human_RBP_ID_9325026,Human_RBP_ID_18676967,Human_RBP_ID_26942047,Human_RBP_ID_27239926 Human_Splice_Rec_1698089,Human_Splice_Rec_1698111 Clinvar_Rec_267 66400 RMVar_ID_66400 Human_SNP_ID_599100447 m1A Human chr16 + 28846305 28846305 28846305 CGCGCCCCGGTAACCGGGGAGCCGGGACCAGGAGCCCGAGCGCACAGAAGAAGAAGGGCGCCTGC CGCGCCCCGGTAACCGGGGAGCCGGGACCAGGGGCCCGAGCGCACAGAAGAAGAAGGGCGCCTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28846176..28846350 26863196 MeRIP-seq:(Medium) rs1380781523 Functional Loss SNV dbSNP153 33..33 33 - - - 66401 RMVar_ID_66401 Human_SNP_ID_599105752 m1A Human chr16 - 28860053 28860053 28860053 GAATCAGTAGAGAGGATGGTCGCTGAAGGAGCAAGGTTGCGGAGAAGGTTGGTGGGGACGTTATC GAATCAGTAGAGAGGATGGTCGCTGAAGGAGCCAGGTTGCGGAGAAGGTTGGTGGGGACGTTATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28860046..28860227 26863196 MeRIP-seq:(Medium) rs1430408991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6506334 66402 RMVar_ID_66402 Human_SNP_ID_599105911 m1A Human chr16 + 28860653 28860653 28860653 ACGCAGCAGTCTCTTAGTTATCAATGCCTTCTAGAGACCATGGCAGCACACCCTGTGATCCCCCA ACGCAGCAGTCTCTTAGTTATCAATGCCTTCTGGAGACCATGGCAGCACACCCTGTGATCCCCCA A G SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28860646..28860726 26863196 MeRIP-seq:(Medium) rs1283590996 Functional Loss SNV dbSNP153 33..33 33 - - - 66403 RMVar_ID_66403 Human_SNP_ID_599107047 m1A Human chr16 + 28864044 28864044 28864044 CCGAGAGGATTCCTGGGTGGGGGTGGGCGTGGAGGGCCGGGGGCTGGAGAGGCACTCGGCCCCGG CCGAGAGGATTCCTGGGTGGGGGTGGGCGTGGGGGGCCGGGGGCTGGAGAGGCACTCGGCCCCGG A G SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28863794..28864494 26863196 MeRIP-seq:(Medium) rs1231593289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235132,Human_RBP_ID_261473,Human_RBP_ID_888585,Human_RBP_ID_3502661,Human_RBP_ID_5236579,Human_RBP_ID_5360003,Human_RBP_ID_9419171,Human_RBP_ID_18418704,Human_RBP_ID_22582341,Human_RBP_ID_26779221,Human_RBP_ID_27837819 66404 RMVar_ID_66404 Human_SNP_ID_599107993 m1A Human chr16 - 28866813 28866813 28866813 CTTCCCTCTGCACCATCCCTGCTCCATCCTTCAAGGCGCCCCCTCCCCGACTGAGTCTCAGCCTC CTTCCCTCTGCACCATCCCTGCTCCATCCTTCGAGGCGCCCCCTCCCCGACTGAGTCTCAGCCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28866691..28867212 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 66405 RMVar_ID_66405 Human_SNP_ID_599108003 m1A Human chr16 + 28866844 28866844 28866844 TTGAAGGATGGAGCAGGGATGGTGCAGAGGGAAGAGCTGCTGAGTTTCATGGGGGCTGAGGAGGC TTGAAGGATGGAGCAGGGATGGTGCAGAGGGAGGAGCTGCTGAGTTTCATGGGGGCTGAGGAGGC A G SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28866745..28867025 26863196 MeRIP-seq:(Medium) rs777056963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5232,Human_RBP_ID_889597,Human_RBP_ID_3502672,Human_RBP_ID_3949048,Human_RBP_ID_5181911,Human_RBP_ID_5357871,Human_RBP_ID_6506389,Human_RBP_ID_22712206,Human_RBP_ID_26328846,Human_RBP_ID_26780322 Human_miRNA_ID_2956237 RMVar_hsa_circ_372710,RMVar_hsa_circ_177679 66406 RMVar_ID_66406 Human_SNP_ID_599108794 m1A Human chr16 - 28869345 28869345 28869345 ACAGGCGGTCATTGCTCTCGCTGGGTCCAAGCAGCAGGTCCTGGCTGGGTAGACTCTCCGAGTGA ACAGGCGGTCATTGCTCTCGCTGGGTCCAAGCGGCAGGTCCTGGCTGGGTAGACTCTCCGAGTGA T C ATP2A1-AS1 RNACentral:URS0000D5B6D3 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28869294..28871891 26863196 MeRIP-seq:(Medium) rs746191403 Functional Loss SNV dbSNP153 33..33 33 - - - 66407 RMVar_ID_66407 Human_SNP_ID_599109055 m1A Human chr16 + 28870352 28870352 28870352 CCCTGAGCAGCACAAGCAGGAATCACGTTGGGAGCTCAGGAGGAAGAGAGCAGGGGAAGGTGGGA CCCTGAGCAGCACAAGCAGGAATCACGTTGGGTGCTCAGGAGGAAGAGAGCAGGGGAAGGTGGGA A T SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28870348..28870526 26863196 MeRIP-seq:(Medium) rs1002288394 Functional Loss SNV dbSNP153 33..33 33 - - - 66408 RMVar_ID_66408 Human_SNP_ID_599109506 m1A Human chr16 + 28871880 28871880 28871880 TCCCATTTTGACTCGATGGAACTGCTTCCCCCAGAGTTGCCCCCCCGCATCCCCATTGAAGAGGG TCCCATTTTGACTCGATGGAACTGCTTCCCCCCGAGTTGCCCCCCCGCATCCCCATTGAAGAGGG A C SH2B1 Ensembl:ENSG00000178188 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28871829..28871916 26863196 MeRIP-seq:(Medium) rs747661965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947532,Human_RBP_ID_12712812 Human_miRNA_ID_2946026 RMVar_hsa_circ_45047,RMVar_hsa_circ_104591,RMVar_hsa_circ_177680 66409 RMVar_ID_66409 Human_SNP_ID_599109507 m1A Human chr16 + 28871880 28871880 28871880 TCCCATTTTGACTCGATGGAACTGCTTCCCCCAGAGTTGCCCCCCCGCATCCCCATTGAAGAGGG TCCCATTTTGACTCGATGGAACTGCTTCCCCCGGAGTTGCCCCCCCGCATCCCCATTGAAGAGGG A G SH2B1 Ensembl:ENSG00000178188 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28871829..28871916 26863196 MeRIP-seq:(Medium) rs747661965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947532,Human_RBP_ID_12712812 Human_miRNA_ID_2946026 RMVar_hsa_circ_45047,RMVar_hsa_circ_104591,RMVar_hsa_circ_177680 66410 RMVar_ID_66410 Human_SNP_ID_599110170 m1A Human chr16 + 28873556 28873556 28873556 GAGGCGTCGAGGGCGCCAGAAGTGGCGGCAGCAGCAGCCGCAGCAGCCAAAGAGAGGCAAGAGAA GAGGCGTCGAGGGCGCCAGAAGTGGCGGCAGCGGCAGCCGCAGCAGCCAAAGAGAGGCAAGAGAA A G SH2B1 Ensembl:ENSG00000178188 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28873176..28873785 26863196 MeRIP-seq:(Medium) rs1212183253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9374117,Human_RBP_ID_18985891,Human_RBP_ID_26328850 66411 RMVar_ID_66411 Human_SNP_ID_599110171 m1A Human chr16 + 28873559 28873559 28873559 GCGTCGAGGGCGCCAGAAGTGGCGGCAGCAGCAGCCGCAGCAGCCAAAGAGAGGCAAGAGAAAGA GCGTCGAGGGCGCCAGAAGTGGCGGCAGCAGCGGCCGCAGCAGCCAAAGAGAGGCAAGAGAAAGA A G SH2B1 Ensembl:ENSG00000178188 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:28873551..28873721 26863196 MeRIP-seq:(Medium) rs755758434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9374117,Human_RBP_ID_18985891,Human_RBP_ID_26328850 66412 RMVar_ID_66412 Human_SNP_ID_599111758 m1A Human chr16 + 28879057 28879057 28879057 ACAAAGTCTTGGGTGTGGGGGGCATGAGGCTGAACCCCAAATGAATCTGTCCTTTTCTTCTTTTT ACAAAGTCTTGGGTGTGGGGGGCATGAGGCTGTACCCCAAATGAATCTGTCCTTTTCTTCTTTTT A T ATP2A1 Ensembl:ENSG00000196296 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28879023..28879136 26863196 MeRIP-seq:(Medium) rs773792059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22541443,Human_RBP_ID_22653024 Human_Splice_Rec_1698291,Human_Splice_Rec_1698333,Human_Splice_Rec_1698375 66413 RMVar_ID_66413 Human_SNP_ID_599112010 m1A Human chr16 - 28879739 28879739 28879739 TGCCTCTGGGGTGCAGGGGAGGAGAGAGGAGGACGCGAATCACACCCGCTGCTGCGCGCCAGCCC TGCCTCTGGGGTGCAGGGGAGGAGAGAGGAGGTCGCGAATCACACCCGCTGCTGCGCGCCAGCCC T A ATP2A1-AS1 Ensembl:ENSG00000260442 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28879329..28879891 26863196 MeRIP-seq:(Medium) rs1014069201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4398312,Human_RBP_ID_5183765,Human_RBP_ID_5576057,Human_RBP_ID_27239958 66414 RMVar_ID_66414 Human_SNP_ID_599113201 m1A Human chr16 - 28883741 28883741 28883741 AAACAGGTGTGGAAGAGTGGGGCGGGCAGCACAGGCTGGAGAGTGAATGGGTGGAGGTGAGGCCA AAACAGGTGTGGAAGAGTGGGGCGGGCAGCACGGGCTGGAGAGTGAATGGGTGGAGGTGAGGCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28883731..28883935 26863196 MeRIP-seq:(Medium) rs932076113 Functional Loss SNV dbSNP153 33..33 33 - - - 66415 RMVar_ID_66415 Human_SNP_ID_599119437 m1A Human chr16 - 28904954 28904954 28904954 ATGAGGCGCCACTCACGGACGTCAGGGACATCAAGGACACCTGAGGGGTCAGGATATCCCCACCC ATGAGGCGCCACTCACGGACGTCAGGGACATCGAGGACACCTGAGGGGTCAGGATATCCCCACCC T C RABEP2 Ensembl:ENSG00000177548 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28904905..28904986 26863196 MeRIP-seq:(Medium) rs1256545426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1698468,Human_Splice_Rec_1698492,Human_Splice_Rec_1698514 66416 RMVar_ID_66416 Human_SNP_ID_599119750 m1A Human chr16 - 28905742 28905742 28905742 GCCCTGACTTCCCAGCCTCCCTGTGCAGCCTGAGGACAGAGATGGAGCGGGTGCAGCAGGAACAG GCCCTGACTTCCCAGCCTCCCTGTGCAGCCTGGGGACAGAGATGGAGCGGGTGCAGCAGGAACAG T C RABEP2 Ensembl:ENSG00000177548 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:28904966..28906129;chr16:28905015..28906153 26863196 MeRIP-seq:(Medium) rs1049183992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889600,Human_RBP_ID_18983565,Human_RBP_ID_22541450 Human_Splice_Rec_1698464,Human_Splice_Rec_1698465,Human_Splice_Rec_1698488,Human_Splice_Rec_1698489,Human_Splice_Rec_1698510,Human_Splice_Rec_1698511 RMVar_hsa_circ_6058 66417 RMVar_ID_66417 Human_SNP_ID_599119902 m1A Human chr16 + 28906054 28906054 28906054 TCTCCTCCCGCTGCACCCTCAGCTGCCCCTCCAGGCTGGCCCTGGCCACTGTCTCCTCCTCCAGA TCTCCTCCCGCTGCACCCTCAGCTGCCCCTCCTGGCTGGCCCTGGCCACTGTCTCCTCCTCCAGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28905756..28906153 26863196 MeRIP-seq:(Medium) rs1415256908 Functional Loss SNV dbSNP153 33..33 33 - - - 66418 RMVar_ID_66418 Human_SNP_ID_599121376 m1A Human chr16 - 28911204 28911204 28911204 GTGGTGAGGGGGGCCAAGTTCCTGGGAGATGCAGGCTGAAGGCAGGGTCTGTGGCAGGGCCGACA GTGGTGAGGGGGGCCAAGTTCCTGGGAGATGCGGGCTGAAGGCAGGGTCTGTGGCAGGGCCGACA T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28911200..28911297 26863196 MeRIP-seq:(Medium) rs545718664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891846 66419 RMVar_ID_66419 Human_SNP_ID_599125086 m1A Human chr16 - 28924481 28924481 28924481 AAACCATGAAGGCTGTGGCAGAGGTGAGCGAGAGCACGAAGGCCGAGGCTGTGGCTGCGGTGCAG AAACCATGAAGGCTGTGGCAGAGGTGAGCGAGGGCACGAAGGCCGAGGCTGTGGCTGCGGTGCAG T C RABEP2 Ensembl:ENSG00000177548 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28924371..28924679 26863196 MeRIP-seq:(Medium) rs763953841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1698451,Human_Splice_Rec_1698471,Human_Splice_Rec_1698517,Human_Splice_Rec_1698527,Human_Splice_Rec_1698535,Human_Splice_Rec_1698555,Human_Splice_Rec_1698561,Human_Splice_Rec_1698565,Human_Splice_Rec_1698571,Human_Splice_Rec_1698573,Human_Splice_Rec_1698575 66420 RMVar_ID_66420 Human_SNP_ID_599125087 m1A Human chr16 - 28924481 28924481 28924481 AAACCATGAAGGCTGTGGCAGAGGTGAGCGAGAGCACGAAGGCCGAGGCTGTGGCTGCGGTGCAG AAACCATGAAGGCTGTGGCAGAGGTGAGCGAGCGCACGAAGGCCGAGGCTGTGGCTGCGGTGCAG T G RABEP2 Ensembl:ENSG00000177548 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28924371..28924679 26863196 MeRIP-seq:(Medium) rs763953841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1698451,Human_Splice_Rec_1698471,Human_Splice_Rec_1698517,Human_Splice_Rec_1698527,Human_Splice_Rec_1698535,Human_Splice_Rec_1698555,Human_Splice_Rec_1698561,Human_Splice_Rec_1698565,Human_Splice_Rec_1698571,Human_Splice_Rec_1698573,Human_Splice_Rec_1698575 66421 RMVar_ID_66421 Human_SNP_ID_599125411 m1A Human chr16 + 28925177 28925177 28925177 CCGGCGCAGCTGCCGCCATTGCCTCAGCGCAAACGGCGGATTCCCGCACTCCCTGGTGACGGAGC CCGGCGCAGCTGCCGCCATTGCCTCAGCGCAAGCGGCGGATTCCCGCACTCCCTGGTGACGGAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28924906..28925209 26863196 MeRIP-seq:(Medium) rs1567500992 Functional Loss SNV dbSNP153 33..33 33 - - - 66422 RMVar_ID_66422 Human_SNP_ID_599128639 m1A Human chr16 + 28936883 28936883 28936883 AAGGCCTCGGCCCTAGATTTAGATTCCGCCCCAGGGTTCAAGGCCGGGTTCCTAGACCCAGAGTC AAGGCCTCGGCCCTAGATTTAGATTCCGCCCCGGGGTTCAAGGCCGGGTTCCTAGACCCAGAGTC A G CD19 Ensembl:ENSG00000177455 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28936848..28936937 26863196 MeRIP-seq:(Medium) rs1275762831 Functional Loss SNV dbSNP153 33..33 33 - - - 66423 RMVar_ID_66423 Human_SNP_ID_599132368 m1A Human chr16 - 28951025 28951025 28951025 CGCTACCTCCGGACCAGCGGCCCCGCTTCCCCACAGGCTCCGCCATGGCACACTTTCCTCCACAA CGCTACCTCCGGACCAGCGGCCCCGCTTCCCCCCAGGCTCCGCCATGGCACACTTTCCTCCACAA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:28951001..28951367 26863196 MeRIP-seq:(Medium) rs764603587 Functional Loss SNV dbSNP153 33..33 33 - - - 66424 RMVar_ID_66424 Human_SNP_ID_599132384 m1A Human chr16 - 28951042 28951042 28951042 ACCCCCTCGGCCGGCACCGCTACCTCCGGACCAGCGGCCCCGCTTCCCCACAGGCTCCGCCATGG ACCCCCTCGGCCGGCACCGCTACCTCCGGACCTGCGGCCCCGCTTCCCCACAGGCTCCGCCATGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28950998..28951375 26863196 MeRIP-seq:(Medium) rs577511088 Functional Loss SNV dbSNP153 33..33 33 - - - 66425 RMVar_ID_66425 Human_SNP_ID_599132460 m1A Human chr16 + 28951190 28951190 28951190 CTTGGTCACCGACAGCGATGAGGAAATTCTGGAGGTCGCCACCGCTCGCGGTGCCGCGGACGAGG CTTGGTCACCGACAGCGATGAGGAAATTCTGGGGGTCGCCACCGCTCGCGGTGCCGCGGACGAGG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28950903..28951438 26863196 MeRIP-seq:(Medium) rs1401241331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4361205,Human_RBP_ID_22944431,Human_RBP_ID_26328854 RMVar_hsa_circ_81983,RMVar_hsa_circ_177691 66426 RMVar_ID_66426 Human_SNP_ID_599133493 m1A Human chr16 + 28954773 28954773 28954773 GGAGGCAGGCAGGACTCTTGGGTGACTCCTGAAAGGTTAAGAAGAAGGGATAGAAGGACTGTTGA GGAGGCAGGCAGGACTCTTGGGTGACTCCTGACAGGTTAAGAAGAAGGGATAGAAGGACTGTTGA A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28954722..28954796 26863196 MeRIP-seq:(Medium) rs193251347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888595,Human_RBP_ID_5360025,Human_RBP_ID_5571662,Human_RBP_ID_9372600,Human_RBP_ID_12713093,Human_RBP_ID_18418978,Human_RBP_ID_18985929,Human_RBP_ID_19073961,Human_RBP_ID_20168944,Human_RBP_ID_22356514,Human_RBP_ID_23274502,Human_RBP_ID_24544508 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 66427 RMVar_ID_66427 Human_SNP_ID_599138659 m1A Human chr16 - 28974865 28974865 28974865 GAGGGCACGATCCCACGCGGAGGCCACCCCTCACCCGGGGTAGGAGCCCGCTGCACTTGCTGTCG GAGGGCACGATCCCACGCGGAGGCCACCCCTCCCCCGGGGTAGGAGCCCGCTGCACTTGCTGTCG T G AC109460.1 Ensembl:ENSG00000260367 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28974820..28978578 26863196 MeRIP-seq:(Medium) rs974818081 Functional Loss SNV dbSNP153 33..33 33 - - - 66428 RMVar_ID_66428 Human_SNP_ID_599138678 m1A Human chr16 - 28974898 28974898 28974898 TACACGTGATGTCGGGGACAGGAGCGGGCTGAAGAGGGCACGATCCCACGCGGAGGCCACCCCTC TACACGTGATGTCGGGGACAGGAGCGGGCTGAGGAGGGCACGATCCCACGCGGAGGCCACCCCTC T C AC109460.1 Ensembl:ENSG00000260367 lincRNA exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr16:28974847..28974947 26863410 MeRIP-seq:(Medium) rs1395025587 Functional Loss SNV dbSNP153 33..33 33 - - - 66429 RMVar_ID_66429 Human_SNP_ID_599140628 m1A Human chr16 + 28982011 28982011 28982011 ATTCCTGCTGCGTTCCCGCGTGGTCCTTGGGGAGACCCCACCCTGCCTTCCCGGAGACTCCTGCT ATTCCTGCTGCGTTCCCGCGTGGTCCTTGGGGGGACCCCACCCTGCCTTCCCGGAGACTCCTGCT A G SPNS1,AC109460.3 Ensembl:ENSG00000169682,Ensembl:ENSG00000261067 Protein coding,lincRNA CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28981961..28982071 26863196 MeRIP-seq:(Medium) rs919595466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_893060,Human_RBP_ID_3510133,Human_RBP_ID_8188987,Human_RBP_ID_18677080,Human_RBP_ID_22441905 Human_Splice_Rec_1698747,Human_Splice_Rec_1698777,Human_Splice_Rec_1698801,Human_Splice_Rec_1698861 Human_miRNA_ID_2932595,Human_miRNA_ID_2932596,Human_miRNA_ID_3204999 RMVar_hsa_circ_535,RMVar_hsa_circ_124899,RMVar_hsa_circ_332764,RMVar_hsa_circ_177700,RMVar_hsa_circ_82062,RMVar_hsa_circ_305040,RMVar_hsa_circ_177702,RMVar_hsa_circ_177703 66430 RMVar_ID_66430 Human_SNP_ID_599223724 m1A Human chr16 - 29298549 29298549 29298549 GTTCATTCATCTGTCCACTCGTCTACCCATACACCCACCTGTTCATTCATCTATCCACTCGTCCA GTTCATTCATCTGTCCACTCGTCTACCCATACCCCCACCTGTTCATTCATCTATCCACTCGTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29298485..29298592 26863196 MeRIP-seq:(Medium) rs946928560 Functional Loss SNV dbSNP153 33..33 33 - - - 66431 RMVar_ID_66431 Human_SNP_ID_599269192 m1A Human chr16 - 29520292 29520292 29520292 CATAAAGTACATTGTCAAGGGTGAGGAGAATTACAAAGAAACTTCTTAAGGGTGGGGGAGATGAT CATAAAGTACATTGTCAAGGGTGAGGAGAATTGCAAAGAAACTTCTTAAGGGTGGGGGAGATGAT T C lnc-NPIPB12-1 RNACentral:URS0000D57D7F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29520254..29520337 26863196 MeRIP-seq:(Medium) rs1425898495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12714010 RMVar_hsa_circ_86611,RMVar_hsa_circ_111408,RMVar_hsa_circ_120069,RMVar_hsa_circ_119566,RMVar_hsa_circ_96331,RMVar_hsa_circ_98651,RMVar_hsa_circ_177709,RMVar_hsa_circ_177711,RMVar_hsa_circ_177712,RMVar_hsa_circ_177713,RMVar_hsa_circ_177710,RMVar_hsa_circ_120916,RMVar_hsa_circ_177717,RMVar_hsa_circ_177716 66432 RMVar_ID_66432 Human_SNP_ID_599282952 m1A Human chr16 + 29595067 29595067 29595067 CGCTGCCGACACCCCGCTCCGGCCCGGGGCTGAGGAGGAAGCCGAGGAGGAGGAAGAGAAGGAGG CGCTGCCGACACCCCGCTCCGGCCCGGGGCTGTGGAGGAAGCCGAGGAGGAGGAAGAGAAGGAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29595057..29595316 26863196 MeRIP-seq:(Medium) rs1420215440 Functional Loss SNV dbSNP153 33..33 33 - - - 66433 RMVar_ID_66433 Human_SNP_ID_599283049 m1A Human chr16 + 29595133 29595130 29595134 GGAGGAGGAGGAGGAGGAGGAGGCGGCGGCGGAGGGCGGGGTAAGAGGACGGCCGTTCCGGGTTC GGAGGAGGAGGAGGAGGAGGAGGCGGCGGC____GGCGGGGTAAGAGGACGGCCGTTCCGGGTTC CGGAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29595086..29595294 26863196 MeRIP-seq:(Medium) rs1260178654 Functional Loss DEL dbSNP153 31..34 33 - - - 66434 RMVar_ID_66434 Human_SNP_ID_599283050 m1A Human chr16 + 29595133 29595133 29595133 GGAGGAGGAGGAGGAGGAGGAGGCGGCGGCGGAGGGCGGGGTAAGAGGACGGCCGTTCCGGGTTC GGAGGAGGAGGAGGAGGAGGAGGCGGCGGCGGCGGGCGGGGTAAGAGGACGGCCGTTCCGGGTTC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29595086..29595294 26863196 MeRIP-seq:(Medium) rs1365613618 Functional Loss SNV dbSNP153 33..33 33 - - - 66435 RMVar_ID_66435 Human_SNP_ID_599283052 m1A Human chr16 + 29595144 29595134 29595144 AGGAGGAGGAGGCGGCGGCGGAGGGCGGGGTAAGAGGACGGCCGTTCCGGGTTCCGCCTGAGCCC AGGAGGAGGAGGCGGCGGCGGAG__________GAGGACGGCCGTTCCGGGTTCCGCCTGAGCCC GGGCGGGGTAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29595136..29595285 26863196 MeRIP-seq:(Medium) rs1443298765 Functional Loss DEL dbSNP153 24..33 33 - - - 66436 RMVar_ID_66436 Human_SNP_ID_599283055 m1A Human chr16 + 29595144 29595138 29595144 AGGAGGAGGAGGCGGCGGCGGAGGGCGGGGTAAGAGGACGGCCGTTCCGGGTTCCGCCTGAGCCC AGGAGGAGGAGGCGGCGGCGGAGGGCG______GAGGACGGCCGTTCCGGGTTCCGCCTGAGCCC GGGGTAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29595136..29595285 26863196 MeRIP-seq:(Medium) rs1430412416 Functional Loss DEL dbSNP153 28..33 33 - - - 66437 RMVar_ID_66437 Human_SNP_ID_599284575 m1A Human chr16 + 29600719 29600719 29600719 TTCTCCACTGATAGACAGCCCCCACCATCTCCACCGACAGACAGCCCCCACCTTCTCCACCGACA TTCTCCACTGATAGACAGCCCCCACCATCTCCCCCGACAGACAGCCCCCACCTTCTCCACCGACA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29600669..29600942 26863196 MeRIP-seq:(Medium) rs1459785153 Functional Loss SNV dbSNP153 33..33 33 - - - 66438 RMVar_ID_66438 Human_SNP_ID_599284648 m1A Human chr16 + 29600869 29600869 29600869 CCCACCTTCTCCACCGACAGACAGCCCCCACCATCTTCACCGACAGACAGCCCCCACCATCTCCA CCCACCTTCTCCACCGACAGACAGCCCCCACCCTCTTCACCGACAGACAGCCCCCACCATCTCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29600820..29600954 26863196 MeRIP-seq:(Medium) rs75995101 Functional Loss SNV dbSNP153 33..33 33 - - - 66439 RMVar_ID_66439 Human_SNP_ID_599284649 m1A Human chr16 + 29600869 29600869 29600869 CCCACCTTCTCCACCGACAGACAGCCCCCACCATCTTCACCGACAGACAGCCCCCACCATCTCCA CCCACCTTCTCCACCGACAGACAGCCCCCACCGTCTTCACCGACAGACAGCCCCCACCATCTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29600820..29600954 26863196 MeRIP-seq:(Medium) rs75995101 Functional Loss SNV dbSNP153 33..33 33 - - - 66440 RMVar_ID_66440 Human_SNP_ID_599284650 m1A Human chr16 + 29600869 29600869 29600869 CCCACCTTCTCCACCGACAGACAGCCCCCACCATCTTCACCGACAGACAGCCCCCACCATCTCCA CCCACCTTCTCCACCGACAGACAGCCCCCACCTTCTTCACCGACAGACAGCCCCCACCATCTCCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29600820..29600954 26863196 MeRIP-seq:(Medium) rs75995101 Functional Loss SNV dbSNP153 33..33 33 - - - 66441 RMVar_ID_66441 Human_SNP_ID_599284735 m1A Human chr16 - 29601131 29601131 29601131 TTCTGGAGCCCAGGGGTGGTGACGTGTCCATCAGGGAAGCACGCGCCTGTGCTGGGGGGTGCTCC TTCTGGAGCCCAGGGGTGGTGACGTGTCCATCCGGGAAGCACGCGCCTGTGCTGGGGGGTGCTCC T G piR-31680 RNACentral:URS00001776ED piRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29601125..29601251 26863196 MeRIP-seq:(Medium) rs1243232570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2472827 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66442 RMVar_ID_66442 Human_SNP_ID_599287990 m1A Human chr16 + 29613561 29613561 29613561 CCGGCGCCGCGCCGTCCGCGCGCTTGGAGGCCAGCATCTTCTCCCGCGCCTCTTCCTTCTCCTCG CCGGCGCCGCGCCGTCCGCGCGCTTGGAGGCCGGCATCTTCTCCCGCGCCTCTTCCTTCTCCTCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:29613526..29613700 26863196 MeRIP-seq:(Medium) rs1318314740 Functional Loss SNV dbSNP153 33..33 33 - - - 66443 RMVar_ID_66443 Human_SNP_ID_599288011 m1A Human chr16 + 29613609 29613609 29613609 CCTCTTCCTTCTCCTCGGCCACCGGGGCCGCTAGCGCCCGCCGCTTCGGGCCCGCACCCGCCATG CCTCTTCCTTCTCCTCGGCCACCGGGGCCGCTGGCGCCCGCCGCTTCGGGCCCGCACCCGCCATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29613498..29613698 26863196 MeRIP-seq:(Medium) rs746569916 Functional Loss SNV dbSNP153 33..33 33 - - - 66444 RMVar_ID_66444 Human_SNP_ID_599306343 m1A Human chr16 + 29683832 29683832 29683832 GAAAAGCTCCCTGTGATTCTGGTGTGCAGCCCAGGCAGAGGCCCCACTGTGTCCACTTCTCTTGA GAAAAGCTCCCTGTGATTCTGGTGTGCAGCCCGGGCAGAGGCCCCACTGTGTCCACTTCTCTTGA A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:29683827..29683959 26863196 MeRIP-seq:(Medium) rs1381209344 Functional Loss SNV dbSNP153 33..33 33 - - - 66445 RMVar_ID_66445 Human_SNP_ID_599309260 m1A Human chr16 - 29694774 29694764 29694775 CCCAGGGGATTTGGCCCACAGCGCCGCCTGCGAGGGGCCTGCCCCGCTGACCAAGGCTGCGTAGT CCCAGGGGATTTGGCCCACAGCGCCGCCTGC___________CCCGCTGACCAAGGCTGCGTAGT GGCAGGCCCCTC G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29694751..29694775 26863196 MeRIP-seq:(Medium) rs756261017 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66446 RMVar_ID_66446 Human_SNP_ID_599309276 m1A Human chr16 + 29694796 29694796 29694796 GGCAGGCCCCTCGCAGGCGGCGCTGTGGGCCAAATCCCCTGGGGTACTGGCAGGGCAGCCTTTCT GGCAGGCCCCTCGCAGGCGGCGCTGTGGGCCAGATCCCCTGGGGTACTGGCAGGGCAGCCTTTCT A G QPRT Ensembl:ENSG00000103485 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29694709..29695159 32194978 MeRIP-seq:(Medium) rs1243764468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471996,Human_RBP_ID_1003848,Human_RBP_ID_4394538,Human_RBP_ID_5495404,Human_RBP_ID_17253831,Human_RBP_ID_17874901,Human_RBP_ID_18190447,Human_RBP_ID_22441399 RMVar_hsa_circ_39933 66447 RMVar_ID_66447 Human_SNP_ID_599309414 m1A Human chr16 - 29695111 29695111 29695111 CCAGGTCGTAGCGGTGCGAGGCGGCCCCGCCCACCAGGAGCCCATACTTCTCCACCAGCCGGAAG CCAGGTCGTAGCGGTGCGAGGCGGCCCCGCCCGCCAGGAGCCCATACTTCTCCACCAGCCGGAAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:29695060..29695200 26863196 MeRIP-seq:(Medium) rs1266065481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66448 RMVar_ID_66448 Human_SNP_ID_599310323 m1A Human chr16 + 29698327 29698327 29698327 GCCTAGTTTACAAGACAGGAGGAAAGAGAGAAAGCAAAAAGTTAGAAAACAAAACAAAACAGAAG GCCTAGTTTACAAGACAGGAGGAAAGAGAGAAGGCAAAAAGTTAGAAAACAAAACAAAACAGAAG A G QPRT Ensembl:ENSG00000103485 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29698278..29698384 26863196 MeRIP-seq:(Medium) rs1337451216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182512 66449 RMVar_ID_66449 Human_SNP_ID_599334483 m1A Human chr16 + 29790778 29790778 29790778 AAGGAGGGAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCT AAGGAGGGAGTGGAATGGCCGCGGGCGGCTCGGCGCAGCAGAGGCGACGCGAGATGGCGGCAGCT A G KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746115237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66450 RMVar_ID_66450 Human_SNP_ID_599334484 m1A Human chr16 + 29790778 29790778 29790778 AAGGAGGGAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCT AAGGAGGGAGTGGAATGGCCGCGGGCGGCTCGTCGCAGCAGAGGCGACGCGAGATGGCGGCAGCT A T KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746115237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66451 RMVar_ID_66451 Human_SNP_ID_599334489 m1A Human chr16 + 29790782 29790782 29790782 AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCCGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG A C KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:29790726..29790915;chr16:29790706..29790975;chr16:29790726..29790971 26863196 MeRIP-seq:(Medium) rs764020056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66452 RMVar_ID_66452 Human_SNP_ID_599334490 m1A Human chr16 + 29790782 29790782 29790782 AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCGGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG A G KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:29790726..29790915;chr16:29790706..29790975;chr16:29790726..29790971 26863196 MeRIP-seq:(Medium) rs764020056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66453 RMVar_ID_66453 Human_SNP_ID_599334491 m1A Human chr16 + 29790782 29790782 29790782 AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG AGGGAGTGGAATGGCCGCGGGCGGCTCGACGCTGCAGAGGCGACGCGAGATGGCGGCAGCTTCAG A T KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:29790726..29790915;chr16:29790706..29790975;chr16:29790726..29790971 26863196 MeRIP-seq:(Medium) rs764020056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66454 RMVar_ID_66454 Human_SNP_ID_599334494 m1A Human chr16 + 29790785 29790785 29790785 GAGTGGAATGGCCGCGGGCGGCTCGACGCAGCAGAGGCGACGCGAGATGGCGGCAGCTTCAGCGG GAGTGGAATGGCCGCGGGCGGCTCGACGCAGCCGAGGCGACGCGAGATGGCGGCAGCTTCAGCGG A C KIF22 Ensembl:ENSG00000079616 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29790726..29790900 26863196 MeRIP-seq:(Medium) rs934601796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233153,Human_RBP_ID_760560,Human_RBP_ID_4393710,Human_RBP_ID_9285733,Human_RBP_ID_18189927,Human_RBP_ID_18419384 Human_Splice_Rec_1699841,Human_Splice_Rec_1699851,Human_Splice_Rec_1699877 RMVar_hsa_circ_103585,RMVar_hsa_circ_112131,RMVar_hsa_circ_177742,RMVar_hsa_circ_177743 66455 RMVar_ID_66455 Human_SNP_ID_599335950 m1A Human chr16 - 29796842 29796839 29796842 CTTTTAGACATGAAGTATGGTGGTAGCAGAAGAAGCAGGGACCAACTTTGCTGGGCGGGCTGGGG CTTTTAGACATGAAGTATGGTGGTAGCAGAAG___CAGGGACCAACTTTGCTGGGCGGGCTGGGG GCTT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:29796833..29796959 26863410 MeRIP-seq:(Medium) rs1449164122 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66456 RMVar_ID_66456 Human_SNP_ID_599335951 m1A Human chr16 - 29796842 29796842 29796842 CTTTTAGACATGAAGTATGGTGGTAGCAGAAGAAGCAGGGACCAACTTTGCTGGGCGGGCTGGGG CTTTTAGACATGAAGTATGGTGGTAGCAGAAGCAGCAGGGACCAACTTTGCTGGGCGGGCTGGGG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:29796833..29796959 26863410 MeRIP-seq:(Medium) rs980543168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66457 RMVar_ID_66457 Human_SNP_ID_599336334 m1A Human chr16 - 29798354 29798351 29798355 GAAGGCATCAAACCTGCAGGAAGAAAGAAAGAAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTGT GAAGGCATCAAACCTGCAGGAAGAAAGAAAG____TAGCGTGTGTGTGTGTGTGTGTGTGTGTGT AATTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29798351..29798400 26863196 MeRIP-seq:(Medium) rs764177021 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66458 RMVar_ID_66458 Human_SNP_ID_599336334 m1A Human chr16 - 29798355 29798351 29798355 AGAAGGCATCAAACCTGCAGGAAGAAAGAAAGAAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTG AGAAGGCATCAAACCTGCAGGAAGAAAGAAAG____TAGCGTGTGTGTGTGTGTGTGTGTGTGTG AATTT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29798351..29798400 26863196 MeRIP-seq:(Medium) rs764177021 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66459 RMVar_ID_66459 Human_SNP_ID_599336336 m1A Human chr16 - 29798355 29798352 29798356 AGAAGGCATCAAACCTGCAGGAAGAAAGAAAGAAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTG AGAAGGCATCAAACCTGCAGGAAGAAAGAAA____TTAGCGTGTGTGTGTGTGTGTGTGTGTGTG ATTTC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29798351..29798400 26863196 MeRIP-seq:(Medium) rs794727510 Functional Loss DEL dbSNP153,HGVD 32..35 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66460 RMVar_ID_66460 Human_SNP_ID_599336337 m1A Human chr16 - 29798354 29798354 29798354 GAAGGCATCAAACCTGCAGGAAGAAAGAAAGAAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTGT GAAGGCATCAAACCTGCAGGAAGAAAGAAAGAGATTAGCGTGTGTGTGTGTGTGTGTGTGTGTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29798351..29798400 26863196 MeRIP-seq:(Medium) rs767740582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66461 RMVar_ID_66461 Human_SNP_ID_599336338 m1A Human chr16 - 29798355 29798355 29798355 AGAAGGCATCAAACCTGCAGGAAGAAAGAAAGAAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTG AGAAGGCATCAAACCTGCAGGAAGAAAGAAAGTAATTAGCGTGTGTGTGTGTGTGTGTGTGTGTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29798351..29798400 26863196 MeRIP-seq:(Medium) rs1037907664 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66462 RMVar_ID_66462 Human_SNP_ID_599336438 m1A Human chr16 - 29798662 29798662 29798662 GGCCCTCGGCACCCTCCTCCCTTGTGAGCTGCAGGAGGTCCATGAGAGCCCGCGGGATCACCCCA GGCCCTCGGCACCCTCCTCCCTTGTGAGCTGCGGGAGGTCCATGAGAGCCCGCGGGATCACCCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29798351..29798753 32194978 MeRIP-seq:(Medium) rs765108503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66463 RMVar_ID_66463 Human_SNP_ID_599336439 m1A Human chr16 - 29798662 29798662 29798662 GGCCCTCGGCACCCTCCTCCCTTGTGAGCTGCAGGAGGTCCATGAGAGCCCGCGGGATCACCCCA GGCCCTCGGCACCCTCCTCCCTTGTGAGCTGCCGGAGGTCCATGAGAGCCCGCGGGATCACCCCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29798351..29798753 32194978 MeRIP-seq:(Medium) rs765108503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66464 RMVar_ID_66464 Human_SNP_ID_599338696 m1A Human chr16 + 29805137 29805137 29805137 GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGAGGGCATAACGGGGAAACAGATGGAGTCCTTCC GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGCGGGCATAACGGGGAAACAGATGGAGTCCTTCC A C KIF22 Ensembl:ENSG00000079616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29804756..29805187 32194978 MeRIP-seq:(Medium) rs772351052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889614,Human_RBP_ID_5355750,Human_RBP_ID_9345801,Human_RBP_ID_18162097,Human_RBP_ID_18677166,Human_RBP_ID_18985966,Human_RBP_ID_19071287,Human_RBP_ID_22654074,Human_RBP_ID_22945023,Human_RBP_ID_23685997 Human_Splice_Rec_1699838,Human_Splice_Rec_1699839,Human_Splice_Rec_1699874,Human_Splice_Rec_1699875,Human_Splice_Rec_1699906,Human_Splice_Rec_1699907,Human_Splice_Rec_1699930,Human_Splice_Rec_1699931,Human_Splice_Rec_1699956,Human_Splice_Rec_1699957 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755 66465 RMVar_ID_66465 Human_SNP_ID_599338697 m1A Human chr16 + 29805137 29805137 29805137 GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGAGGGCATAACGGGGAAACAGATGGAGTCCTTCC GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGGGGGCATAACGGGGAAACAGATGGAGTCCTTCC A G KIF22 Ensembl:ENSG00000079616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29804756..29805187 32194978 MeRIP-seq:(Medium) rs772351052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889614,Human_RBP_ID_5355750,Human_RBP_ID_9345801,Human_RBP_ID_18162097,Human_RBP_ID_18677166,Human_RBP_ID_18985966,Human_RBP_ID_19071287,Human_RBP_ID_22654074,Human_RBP_ID_22945023,Human_RBP_ID_23685997 Human_Splice_Rec_1699838,Human_Splice_Rec_1699839,Human_Splice_Rec_1699874,Human_Splice_Rec_1699875,Human_Splice_Rec_1699906,Human_Splice_Rec_1699907,Human_Splice_Rec_1699930,Human_Splice_Rec_1699931,Human_Splice_Rec_1699956,Human_Splice_Rec_1699957 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755 66466 RMVar_ID_66466 Human_SNP_ID_599338698 m1A Human chr16 + 29805137 29805137 29805137 GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGAGGGCATAACGGGGAAACAGATGGAGTCCTTCC GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGTGGGCATAACGGGGAAACAGATGGAGTCCTTCC A T KIF22 Ensembl:ENSG00000079616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29804756..29805187 32194978 MeRIP-seq:(Medium) rs772351052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889614,Human_RBP_ID_5355750,Human_RBP_ID_9345801,Human_RBP_ID_18162097,Human_RBP_ID_18677166,Human_RBP_ID_18985966,Human_RBP_ID_19071287,Human_RBP_ID_22654074,Human_RBP_ID_22945023,Human_RBP_ID_23685997 Human_Splice_Rec_1699838,Human_Splice_Rec_1699839,Human_Splice_Rec_1699874,Human_Splice_Rec_1699875,Human_Splice_Rec_1699906,Human_Splice_Rec_1699907,Human_Splice_Rec_1699930,Human_Splice_Rec_1699931,Human_Splice_Rec_1699956,Human_Splice_Rec_1699957 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755 66467 RMVar_ID_66467 Human_SNP_ID_599338861 m1A Human chr16 + 29805339 29805339 29805339 CTGACCGTCGTCTCCTCACTCCGCCTTTTCAAATTTTTGTATAACCCCGTGTTGTGTAAATACAG CTGACCGTCGTCTCCTCACTCCGCCTTTTCAACTTTTTGTATAACCCCGTGTTGTGTAAATACAG A C KIF22 Ensembl:ENSG00000079616 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29805202..29805343 26863196 MeRIP-seq:(Medium) rs1054794276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43819,Human_RBP_ID_472054,Human_RBP_ID_1365451,Human_RBP_ID_1516212,Human_RBP_ID_1841109,Human_RBP_ID_2472867,Human_RBP_ID_3493987,Human_RBP_ID_8431734,Human_RBP_ID_17874939,Human_RBP_ID_18677169,Human_RBP_ID_23685998,Human_RBP_ID_24476044,Human_RBP_ID_26942260 Human_Splice_Rec_1699840,Human_Splice_Rec_1699876,Human_Splice_Rec_1699908,Human_Splice_Rec_1699932,Human_Splice_Rec_1699958 Human_miRNA_ID_753069,Human_miRNA_ID_1175591 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755,RMVar_hsa_circ_122261,RMVar_hsa_circ_177757 66468 RMVar_ID_66468 Human_SNP_ID_599338862 m1A Human chr16 + 29805339 29805339 29805339 CTGACCGTCGTCTCCTCACTCCGCCTTTTCAAATTTTTGTATAACCCCGTGTTGTGTAAATACAG CTGACCGTCGTCTCCTCACTCCGCCTTTTCAATTTTTTGTATAACCCCGTGTTGTGTAAATACAG A T KIF22 Ensembl:ENSG00000079616 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29805202..29805343 26863196 MeRIP-seq:(Medium) rs1054794276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43819,Human_RBP_ID_472054,Human_RBP_ID_1365451,Human_RBP_ID_1516212,Human_RBP_ID_1841109,Human_RBP_ID_2472867,Human_RBP_ID_3493987,Human_RBP_ID_8431734,Human_RBP_ID_17874939,Human_RBP_ID_18677169,Human_RBP_ID_23685998,Human_RBP_ID_24476044,Human_RBP_ID_26942260 Human_Splice_Rec_1699840,Human_Splice_Rec_1699876,Human_Splice_Rec_1699908,Human_Splice_Rec_1699932,Human_Splice_Rec_1699958 Human_miRNA_ID_753069,Human_miRNA_ID_1175591 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755,RMVar_hsa_circ_122261,RMVar_hsa_circ_177757 66469 RMVar_ID_66469 Human_SNP_ID_599339126 m1A Human chr16 + 29805763 29805763 29805763 GAGTGGAATCGTTGGCGGGGGGAAGAGGAGAGAAGCCGCCCTGTCTCCCGCGCGCCCACCACCTG GAGTGGAATCGTTGGCGGGGGGAAGAGGAGAGTAGCCGCCCTGTCTCCCGCGCGCCCACCACCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29805701..29805925 26863196 MeRIP-seq:(Medium) rs1174576716 Functional Loss SNV dbSNP153 33..33 33 - - - 66470 RMVar_ID_66470 Human_SNP_ID_599339572 m1A Human chr16 - 29806497 29806491 29806497 GGGCGCCTTGCGGGCCGCGGAGCGCCGCGGCGACGGCGGCGGCGACGCCCCCTGGGTGGGGGCGG GGGCGCCTTGCGGGCCGCGGAGCGCCGCGGCG______GCGGCGACGCCCCCTGGGTGGGGGCGG CCGCCGT C AC009133.2 Ensembl:ENSG00000259952 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:29806401..29806727 26863410 MeRIP-seq:(Medium) rs1191130988 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66471 RMVar_ID_66471 Human_SNP_ID_599339578 m1A Human chr16 - 29806497 29806497 29806497 GGGCGCCTTGCGGGCCGCGGAGCGCCGCGGCGACGGCGGCGGCGACGCCCCCTGGGTGGGGGCGG GGGCGCCTTGCGGGCCGCGGAGCGCCGCGGCGGCGGCGGCGGCGACGCCCCCTGGGTGGGGGCGG T C AC009133.2 Ensembl:ENSG00000259952 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:29806401..29806727 26863410 MeRIP-seq:(Medium) rs1280417894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66472 RMVar_ID_66472 Human_SNP_ID_599339929 m1A Human chr16 + 29807006 29807006 29807006 GCAGGCCGCGCCGGCGCCCCCGCCCACGCCCCAGGCCCCGGCGGCCGAGCCCCTCCAGGTGGACT GCAGGCCGCGCCGGCGCCCCCGCCCACGCCCCGGGCCCCGGCGGCCGAGCCCCTCCAGGTGGACT A G MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:29806551..29807800 26863410 MeRIP-seq:(Medium) rs1232981671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234761,Human_RBP_ID_472072,Human_RBP_ID_817367,Human_RBP_ID_4361668,Human_RBP_ID_5360053,Human_RBP_ID_8812337,Human_RBP_ID_9325047,Human_RBP_ID_18189934,Human_RBP_ID_22532792 Human_Splice_Rec_1699962,Human_Splice_Rec_1699970,Human_Splice_Rec_1699982,Human_Splice_Rec_1699983,Human_Splice_Rec_1699986,Human_Splice_Rec_1699987,Human_Splice_Rec_1699990 Human_miRNA_ID_874317,Human_miRNA_ID_1232692,Human_miRNA_ID_2390807 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 66473 RMVar_ID_66473 Human_SNP_ID_599339930 m1A Human chr16 + 29807006 29807006 29807006 GCAGGCCGCGCCGGCGCCCCCGCCCACGCCCCAGGCCCCGGCGGCCGAGCCCCTCCAGGTGGACT GCAGGCCGCGCCGGCGCCCCCGCCCACGCCCCTGGCCCCGGCGGCCGAGCCCCTCCAGGTGGACT A T MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:29806551..29807800 26863410 MeRIP-seq:(Medium) rs1232981671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234761,Human_RBP_ID_472072,Human_RBP_ID_817367,Human_RBP_ID_4361668,Human_RBP_ID_5360053,Human_RBP_ID_8812337,Human_RBP_ID_9325047,Human_RBP_ID_18189934,Human_RBP_ID_22532792 Human_Splice_Rec_1699962,Human_Splice_Rec_1699970,Human_Splice_Rec_1699982,Human_Splice_Rec_1699983,Human_Splice_Rec_1699986,Human_Splice_Rec_1699987,Human_Splice_Rec_1699990 Human_miRNA_ID_874317,Human_miRNA_ID_1232692,Human_miRNA_ID_2390807 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 66474 RMVar_ID_66474 Human_SNP_ID_599339969 m1A Human chr16 - 29807103 29807068 29807104 GCAGGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGC GCAGGGGCCGGGGGCGCGGCAGCGACGGCGG__________________________________ TCCGCCGCGGCTGCTGCGGCCGCTGCCGCCGCTGCTG T AC009133.2 Ensembl:ENSG00000259952 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:29806376..29807307 26863410 MeRIP-seq:(Medium) rs1234267446 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_816273,Human_RBP_ID_3504459,Human_RBP_ID_8184485 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66475 RMVar_ID_66475 Human_SNP_ID_599339991 m1A Human chr16 - 29807100 29807088 29807100 GGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGCGGA GGGGCCGGGGGCGCGGCAGCGACGGCGGCAGC____________GGCCGCAGCAGCCGCGGCGGA CGCTGCCGCCGCT C AC009133.2 Ensembl:ENSG00000259952 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr16:29806876..29807273;chr16:29806826..29807201 26863410 MeRIP-seq:(Medium) rs779951400 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_816273,Human_RBP_ID_3504459,Human_RBP_ID_8184485 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66476 RMVar_ID_66476 Human_SNP_ID_599339998 m1A Human chr16 - 29807103 29807094 29807103 GCAGGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGC GCAGGGGCCGGGGGCGCGGCAGCGACGGCGGC_________GGCAGCGGCCGCAGCAGCCGCGGC CGCCGCTGCT C AC009133.2 Ensembl:ENSG00000259952 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:29806376..29807307 26863410 MeRIP-seq:(Medium) rs929946715 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_816273,Human_RBP_ID_3504459,Human_RBP_ID_8184485 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66477 RMVar_ID_66477 Human_SNP_ID_599340006 m1A Human chr16 - 29807100 29807100 29807100 GGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGCGGA GGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCCGCGGCGGCAGCGGCCGCAGCAGCCGCGGCGGA T G AC009133.2 Ensembl:ENSG00000259952 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr16:29806876..29807273;chr16:29806826..29807201 26863410 MeRIP-seq:(Medium) rs1047033609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816273,Human_RBP_ID_3504459,Human_RBP_ID_8184485 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66478 RMVar_ID_66478 Human_SNP_ID_599340011 m1A Human chr16 - 29807103 29807103 29807103 GCAGGGGCCGGGGGCGCGGCAGCGACGGCGGCAGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGC GCAGGGGCCGGGGGCGCGGCAGCGACGGCGGCGGCAGCGGCGGCAGCGGCCGCAGCAGCCGCGGC T C AC009133.2 Ensembl:ENSG00000259952 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:29806376..29807307 26863410 MeRIP-seq:(Medium) rs1312960953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816273,Human_RBP_ID_3504459,Human_RBP_ID_8184485 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66479 RMVar_ID_66479 Human_SNP_ID_599340427 m1A Human chr16 + 29807774 29807774 29807774 GGACCGCATGAGCTACCACGTGCGCTCACATGACGGCGCTGTGCACAAGCCCTACAACTGCTCCC GGACCGCATGAGCTACCACGTGCGCTCACATGCCGGCGCTGTGCACAAGCCCTACAACTGCTCCC A C MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:29807726..29807775 26863196 MeRIP-seq:(Medium) rs1468996543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472094,Human_RBP_ID_761114,Human_RBP_ID_1003880,Human_RBP_ID_1516230,Human_RBP_ID_1841117,Human_RBP_ID_3493991,Human_RBP_ID_4398466,Human_RBP_ID_5259189,Human_RBP_ID_6506827,Human_RBP_ID_8431761,Human_RBP_ID_8806725,Human_RBP_ID_12714855,Human_RBP_ID_17253844,Human_RBP_ID_17486022,Human_RBP_ID_18677190,Human_RBP_ID_26942277,Human_RBP_ID_27240061,Human_RBP_ID_27441113 Human_Splice_Rec_1699963,Human_Splice_Rec_1699971,Human_Splice_Rec_1699991,Human_Splice_Rec_1700003,Human_Splice_Rec_1700009,Human_Splice_Rec_1700013 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 66480 RMVar_ID_66480 Human_SNP_ID_599340497 m1A Human chr16 + 29807880 29807880 29807880 CGCCCGCTAGGCCGTGGGGAGGGAGGGACGCGACGGAGGTGGCCTGGCCGTGGCTGGCGGGGAGG CGCCCGCTAGGCCGTGGGGAGGGAGGGACGCGGCGGAGGTGGCCTGGCCGTGGCTGGCGGGGAGG A G MAZ Ensembl:ENSG00000103495 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29807876..29808000 26863196 MeRIP-seq:(Medium) rs1246174758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817369,Human_RBP_ID_5360055,Human_RBP_ID_8231254,Human_RBP_ID_9419176,Human_RBP_ID_19071290,Human_RBP_ID_21971214,Human_RBP_ID_22054965,Human_RBP_ID_22760206,Human_RBP_ID_26780336 Human_Splice_Rec_1700021 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 66481 RMVar_ID_66481 Human_SNP_ID_599340785 m1A Human chr16 + 29808272 29808272 29808272 CTCAACAGTCACGTCAGACAAGTGCACTCAACAGAACGGCCCTTCAAATGTGAGGTAGGAAGCCC CTCAACAGTCACGTCAGACAAGTGCACTCAACCGAACGGCCCTTCAAATGTGAGGTAGGAAGCCC A C MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29808101..29808300 26863196 MeRIP-seq:(Medium) rs1338230791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472098,Human_RBP_ID_1003883,Human_RBP_ID_1281690,Human_RBP_ID_1516238,Human_RBP_ID_1841120,Human_RBP_ID_5419741,Human_RBP_ID_5440351,Human_RBP_ID_5495424,Human_RBP_ID_6506838,Human_RBP_ID_8083125,Human_RBP_ID_8431764,Human_RBP_ID_8806731,Human_RBP_ID_12714867,Human_RBP_ID_17253846,Human_RBP_ID_17369445,Human_RBP_ID_17486023,Human_RBP_ID_17874959,Human_RBP_ID_18285187,Human_RBP_ID_18529743,Human_RBP_ID_18677194,Human_RBP_ID_26810216 Human_Splice_Rec_1699964,Human_Splice_Rec_1699965,Human_Splice_Rec_1699972,Human_Splice_Rec_1699973,Human_Splice_Rec_1699992,Human_Splice_Rec_1699993,Human_Splice_Rec_1699998,Human_Splice_Rec_1699999,Human_Splice_Rec_1700004,Human_Splice_Rec_1700005,Human_Splice_Rec_1700010,Human_Splice_Rec_1700011,Human_Splice_Rec_1700014,Human_Splice_Rec_1700015,Human_Splice_Rec_1700022,Human_Splice_Rec_1700023,Human_Splice_Rec_1700028,Human_Splice_Rec_1700029,Human_Splice_Rec_1700033,Human_Splice_Rec_1700037,Human_Splice_Rec_1700039 Human_miRNA_ID_2022609 RMVar_hsa_circ_26374,RMVar_hsa_circ_81490,RMVar_hsa_circ_177759,RMVar_hsa_circ_75625,RMVar_hsa_circ_323667,RMVar_hsa_circ_177761,RMVar_hsa_circ_177762 66482 RMVar_ID_66482 Human_SNP_ID_599341542 m1A Human chr16 - 29809607 29809607 29809607 TGCACGCTGCACAGCTTGCACAGGATGCGGTCAGCCCGCGGGGCCTGGAGCCCGTGGTCCTTCAC TGCACGCTGCACAGCTTGCACAGGATGCGGTCTGCCCGCGGGGCCTGGAGCCCGTGGTCCTTCAC T A AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29809594..29809761;chr16:29809600..29809712;chr16:29809604..29809744 26863196 MeRIP-seq:(Medium) rs377713456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700047 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66483 RMVar_ID_66483 Human_SNP_ID_599341543 m1A Human chr16 - 29809607 29809607 29809607 TGCACGCTGCACAGCTTGCACAGGATGCGGTCAGCCCGCGGGGCCTGGAGCCCGTGGTCCTTCAC TGCACGCTGCACAGCTTGCACAGGATGCGGTCGGCCCGCGGGGCCTGGAGCCCGTGGTCCTTCAC T C AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29809594..29809761;chr16:29809600..29809712;chr16:29809604..29809744 26863196 MeRIP-seq:(Medium) rs377713456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700047 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66484 RMVar_ID_66484 Human_SNP_ID_599341792 m1A Human chr16 - 29810089 29810089 29810089 CCGCCGCTGCCGCTGCCGCCGCCATTGGACAAACCTCACCAGTACCTGCACAGGAGAAACACCAC CCGCCGCTGCCGCTGCCGCCGCCATTGGACAACCCTCACCAGTACCTGCACAGGAGAAACACCAC T G AC009133.1 Ensembl:ENSG00000238045 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:29810076..29810125;chr16:29810076..29810100 26863196 MeRIP-seq:(Medium) rs189662522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700054 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66485 RMVar_ID_66485 Human_SNP_ID_599341807 m1A Human chr16 + 29810108 29810099 29810108 GGTACTGGTGAGGTTTGTCCAATGGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC GGTACTGGTGAGGTTTGTCCAATG_________GCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC GGCGGCGGCA G MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA CDS,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29810072..29810233 26863196 MeRIP-seq:(Medium) rs748595015 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_234426,Human_RBP_ID_472116,Human_RBP_ID_893214,Human_RBP_ID_1003893,Human_RBP_ID_5097354,Human_RBP_ID_5183917,Human_RBP_ID_5247384,Human_RBP_ID_5259664,Human_RBP_ID_5495426,Human_RBP_ID_5648338,Human_RBP_ID_6506856,Human_RBP_ID_12714910,Human_RBP_ID_17874970,Human_RBP_ID_22532687,Human_RBP_ID_27441119 Human_Splice_Rec_1699968,Human_Splice_Rec_1699976,Human_Splice_Rec_1699980,Human_Splice_Rec_1700002,Human_Splice_Rec_1700008,Human_Splice_Rec_1700018,Human_Splice_Rec_1700026,Human_Splice_Rec_1700036,Human_Splice_Rec_1700044,Human_Splice_Rec_1700046,Human_Splice_Rec_1700062 RMVar_hsa_circ_26374 66486 RMVar_ID_66486 Human_SNP_ID_599341828 m1A Human chr16 + 29810108 29810108 29810108 GGTACTGGTGAGGTTTGTCCAATGGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC GGTACTGGTGAGGTTTGTCCAATGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC A G MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA CDS,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29810072..29810233 26863196 MeRIP-seq:(Medium) rs201662748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234426,Human_RBP_ID_472116,Human_RBP_ID_893214,Human_RBP_ID_1003893,Human_RBP_ID_5097354,Human_RBP_ID_5183917,Human_RBP_ID_5247384,Human_RBP_ID_5259664,Human_RBP_ID_5495426,Human_RBP_ID_5648338,Human_RBP_ID_6506856,Human_RBP_ID_12714910,Human_RBP_ID_17874970,Human_RBP_ID_22532687,Human_RBP_ID_27441119 Human_Splice_Rec_1699968,Human_Splice_Rec_1699976,Human_Splice_Rec_1699980,Human_Splice_Rec_1700002,Human_Splice_Rec_1700008,Human_Splice_Rec_1700018,Human_Splice_Rec_1700026,Human_Splice_Rec_1700036,Human_Splice_Rec_1700044,Human_Splice_Rec_1700046,Human_Splice_Rec_1700062 RMVar_hsa_circ_26374 66487 RMVar_ID_66487 Human_SNP_ID_599341972 m1A Human chr16 - 29810244 29810244 29810244 GGACTCTACTCCATTCTCCCCTCTCCCCCGCAACCAACTTGGAGCTCACCAGGGTTGGGAGGGAA GGACTCTACTCCATTCTCCCCTCTCCCCCGCAGCCAACTTGGAGCTCACCAGGGTTGGGAGGGAA T C AC009133.1 Ensembl:ENSG00000238045 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29808884..29810648 32194978 MeRIP-seq:(Medium) rs1238757887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66488 RMVar_ID_66488 Human_SNP_ID_599342334 m1A Human chr16 + 29810844 29810843 29810845 GCCCTGAACATCGTCCTACTTGAGAATCTGTCAGGGGAAAAAGTCAAGGGGAGCAGGAGGAAGAG GCCCTGAACATCGTCCTACTTGAGAATCTGTC__GGGAAAAAGTCAAGGGGAGCAGGAGGAAGAG CAG C MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:29810747..29810847 32194978 MeRIP-seq:(Medium) rs1173690668 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_472132,Human_RBP_ID_1003904,Human_RBP_ID_1131125,Human_RBP_ID_1281697,Human_RBP_ID_1516278,Human_RBP_ID_1841137,Human_RBP_ID_2472876,Human_RBP_ID_3502678,Human_RBP_ID_3947553,Human_RBP_ID_4361780,Human_RBP_ID_5097357,Human_RBP_ID_5113449,Human_RBP_ID_5141874,Human_RBP_ID_5316635,Human_RBP_ID_5576133,Human_RBP_ID_5648219,Human_RBP_ID_6506896,Human_RBP_ID_8185816,Human_RBP_ID_8431799,Human_RBP_ID_8941335,Human_RBP_ID_12714949,Human_RBP_ID_17067824,Human_RBP_ID_17486033,Human_RBP_ID_17652629,Human_RBP_ID_17874990,Human_RBP_ID_18190460,Human_RBP_ID_18285204,Human_RBP_ID_18677219,Human_RBP_ID_21973054,Human_RBP_ID_22497648,Human_RBP_ID_22800870,Human_RBP_ID_22938164,Human_RBP_ID_23128094,Human_RBP_ID_23163810,Human_RBP_ID_23686033,Human_RBP_ID_26329972,Human_RBP_ID_26445031,Human_RBP_ID_26942323,Human_RBP_ID_27240097,Human_RBP_ID_27657895 Human_miRNA_ID_119918,Human_miRNA_ID_123732,Human_miRNA_ID_959716 66489 RMVar_ID_66489 Human_SNP_ID_599342359 m1A Human chr16 + 29810888 29810888 29810888 CAAGGGGAGCAGGAGGAAGAGCCAGGAGGGCCAGAGGCAGAGAAGAGATGGAGTCTTAGGGGCCA CAAGGGGAGCAGGAGGAAGAGCCAGGAGGGCCGGAGGCAGAGAAGAGATGGAGTCTTAGGGGCCA A G MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29810697..29811114;chr16:29810026..29811175;chr16:29810044..29811175;chr16:29810353..29811175 26863196 MeRIP-seq:(Medium) rs1250713585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472132,Human_RBP_ID_1131125,Human_RBP_ID_1516281,Human_RBP_ID_1841139,Human_RBP_ID_3502678,Human_RBP_ID_3947553,Human_RBP_ID_4361780,Human_RBP_ID_5097357,Human_RBP_ID_5142204,Human_RBP_ID_5576133,Human_RBP_ID_5648254,Human_RBP_ID_6506903,Human_RBP_ID_8185816,Human_RBP_ID_8941336,Human_RBP_ID_12714956,Human_RBP_ID_17652629,Human_RBP_ID_17874990,Human_RBP_ID_18190460,Human_RBP_ID_18285206,Human_RBP_ID_21973055,Human_RBP_ID_23128096,Human_RBP_ID_23163810,Human_RBP_ID_23686034,Human_RBP_ID_25204635,Human_RBP_ID_26328864,Human_RBP_ID_26445031 Human_miRNA_ID_939473,Human_miRNA_ID_955207 66490 RMVar_ID_66490 Human_SNP_ID_599342436 m1A Human chr16 - 29811026 29811024 29811026 CAACTTCTTCTGTCGTGGGGAAGAGGGATGAAAAGACAAGACCAGGGCTGGAGCTGGGGTGGAAG CAACTTCTTCTGTCGTGGGGAAGAGGGATGAA__GACAAGACCAGGGCTGGAGCTGGGGTGGAAG CTT C AC009133.1 Ensembl:ENSG00000238045 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr16:29810876..29811125;chr16:29809611..29811991 26863410 MeRIP-seq:(Medium) rs1242559172 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66491 RMVar_ID_66491 Human_SNP_ID_599343348 m1A Human chr16 + 29813147 29813147 29813147 CCAGGCGAAGGGCCTGGCCATTCTGAAGCTGAAACTGGCCCTCCCCAGGTCCTAGCAGGGGTACC CCAGGCGAAGGGCCTGGCCATTCTGAAGCTGAGACTGGCCCTCCCCAGGTCCTAGCAGGGGTACC A G PRRT2,AC009133.6 Ensembl:ENSG00000167371,Ensembl:ENSG00000280893 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29812460..29813175 32194978 MeRIP-seq:(Medium) rs1315799003 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_7964 66492 RMVar_ID_66492 Human_SNP_ID_599343742 m1A Human chr16 - 29813966 29813966 29813966 TATTGCAGCGCTGGCGGGAAGCTGGGAGCCACAGCAGGCCTGGGCTAGGGTCCCATGGGGCTCAC TATTGCAGCGCTGGCGGGAAGCTGGGAGCCACGGCAGGCCTGGGCTAGGGTCCCATGGGGCTCAC T C AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29813915..29814460 26863196 MeRIP-seq:(Medium) rs770510862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5182677 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66493 RMVar_ID_66493 Human_SNP_ID_599344107 m1A Human chr16 - 29814961 29814960 29814961 GGCCAGGAGAGATGCAGGGAGGCTGAGAGCGCAGAGTTGGGGAGGTGTTCAGGGAGGTTTCCAGA GGCCAGGAGAGATGCAGGGAGGCTGAGAGCGC_GAGTTGGGGAGGTGTTCAGGGAGGTTTCCAGA CT C AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29814926..29815087 26863196 MeRIP-seq:(Medium) rs1342198949 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5182679 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66494 RMVar_ID_66494 Human_SNP_ID_599344793 m1A Human chr16 + 29816719 29816719 29816719 AGAGGAGACCGAGCGTGAGGGGTCCGGGGGCGAGGAGGCGCAGGGAGAAGTCCCCAGCGCTGGGG AGAGGAGACCGAGCGTGAGGGGTCCGGGGGCGCGGAGGCGCAGGGAGAAGTCCCCAGCGCTGGGG A C PAGR1,AC009133.6 Ensembl:ENSG00000280789,Ensembl:ENSG00000280893 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:29816626..29816925;chr16:29816648..29816864 26863196 MeRIP-seq:(Medium) rs746515233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4361811,Human_RBP_ID_5317508,Human_RBP_ID_6506925,Human_RBP_ID_9061676,Human_RBP_ID_9374144,Human_RBP_ID_18983599,Human_RBP_ID_23686047 66495 RMVar_ID_66495 Human_SNP_ID_599344795 m1A Human chr16 + 29816722 29816722 29816722 GGAGACCGAGCGTGAGGGGTCCGGGGGCGAGGAGGCGCAGGGAGAAGTCCCCAGCGCTGGGGGAG GGAGACCGAGCGTGAGGGGTCCGGGGGCGAGGTGGCGCAGGGAGAAGTCCCCAGCGCTGGGGGAG A T PAGR1,AC009133.6 Ensembl:ENSG00000280789,Ensembl:ENSG00000280893 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29816632..29816880 26863196 MeRIP-seq:(Medium) rs1273257711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5317508,Human_RBP_ID_6506925,Human_RBP_ID_9374144,Human_RBP_ID_18983599,Human_RBP_ID_23686047 66496 RMVar_ID_66496 Human_SNP_ID_599345763 m1A Human chr16 - 29819672 29819672 29819672 GGGGGCTGGCGGGGCTGGGGTCCTCCGAGTCCAGGCTGAAGAGGTCCCTCCCGGTACGAAGGATC GGGGGCTGGCGGGGCTGGGGTCCTCCGAGTCCGGGCTGAAGAGGTCCCTCCCGGTACGAAGGATC T C AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29819626..29819800 26863196 MeRIP-seq:(Medium) rs537426155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66497 RMVar_ID_66497 Human_SNP_ID_599348938 m1A Human chr16 + 29830986 29830985 29830987 GATGCCCAGGGCTTGGTGCTGTTTGATGTCACAGGGCAAGTTCGGCTTCGCCACGCTGACCTCGA GATGCCCAGGGCTTGGTGCTGTTTGATGTCAC__GGCAAGTTCGGCTTCGCCACGCTGACCTCGA CAG C MVP Ensembl:ENSG00000013364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29830937..29831707 32194978 MeRIP-seq:(Medium) rs762372440 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1700163,Human_Splice_Rec_1700173,Human_Splice_Rec_1700209,Human_Splice_Rec_1700251,Human_Splice_Rec_1700259,Human_Splice_Rec_1700275 Human_miRNA_ID_3090972 RMVar_hsa_circ_104737,RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_59024,RMVar_hsa_circ_177766,RMVar_hsa_circ_375764,RMVar_hsa_circ_342513,RMVar_hsa_circ_96054,RMVar_hsa_circ_177767,RMVar_hsa_circ_177768 66498 RMVar_ID_66498 Human_SNP_ID_599348939 m1A Human chr16 + 29830986 29830986 29830986 GATGCCCAGGGCTTGGTGCTGTTTGATGTCACAGGGCAAGTTCGGCTTCGCCACGCTGACCTCGA GATGCCCAGGGCTTGGTGCTGTTTGATGTCACGGGGCAAGTTCGGCTTCGCCACGCTGACCTCGA A G MVP Ensembl:ENSG00000013364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29830937..29831707 32194978 MeRIP-seq:(Medium) rs759909189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700163,Human_Splice_Rec_1700173,Human_Splice_Rec_1700209,Human_Splice_Rec_1700251,Human_Splice_Rec_1700259,Human_Splice_Rec_1700275 Human_miRNA_ID_3090972 RMVar_hsa_circ_104737,RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_59024,RMVar_hsa_circ_177766,RMVar_hsa_circ_375764,RMVar_hsa_circ_342513,RMVar_hsa_circ_96054,RMVar_hsa_circ_177767,RMVar_hsa_circ_177768 66499 RMVar_ID_66499 Human_SNP_ID_599349723 m1A Human chr16 + 29833805 29833805 29833805 TCCATCTAAAGGCGCTGCTTGATTTTGAGGATAAAGATGGAGACAAGGTGGTGGCAGGAGATGAG TCCATCTAAAGGCGCTGCTTGATTTTGAGGATTAAGATGGAGACAAGGTGGTGGCAGGAGATGAG A T MVP Ensembl:ENSG00000013364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29833722..29834100 32194978 MeRIP-seq:(Medium) rs763630916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700164,Human_Splice_Rec_1700165,Human_Splice_Rec_1700174,Human_Splice_Rec_1700175,Human_Splice_Rec_1700210,Human_Splice_Rec_1700211,Human_Splice_Rec_1700244,Human_Splice_Rec_1700245,Human_Splice_Rec_1700276,Human_Splice_Rec_1700287,Human_Splice_Rec_1700289 RMVar_hsa_circ_177770,RMVar_hsa_circ_104737,RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_59024,RMVar_hsa_circ_342513,RMVar_hsa_circ_33246,RMVar_hsa_circ_110370,RMVar_hsa_circ_296220,RMVar_hsa_circ_328170,RMVar_hsa_circ_177768,RMVar_hsa_circ_310080,RMVar_hsa_circ_290122,RMVar_hsa_circ_100964,RMVar_hsa_circ_177772,RMVar_hsa_circ_177773,RMVar_hsa_circ_177774,RMVar_hsa_circ_177771,RMVar_hsa_circ_177769 66500 RMVar_ID_66500 Human_SNP_ID_599350279 m1A Human chr16 + 29835644 29835644 29835644 TCTGTCAATCCCCTGTGTCTAAGCTGTGGGGGAGGGGTAGGTGGGGAGCAGGCTGGGGGGCCCTT TCTGTCAATCCCCTGTGTCTAAGCTGTGGGGGGGGGGTAGGTGGGGAGCAGGCTGGGGGGCCCTT A G MVP Ensembl:ENSG00000013364 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29835639..29835722 26863196 MeRIP-seq:(Medium) rs1455155745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177770,RMVar_hsa_circ_104737,RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_59024,RMVar_hsa_circ_33246,RMVar_hsa_circ_110370,RMVar_hsa_circ_328170,RMVar_hsa_circ_177768,RMVar_hsa_circ_310080,RMVar_hsa_circ_290122,RMVar_hsa_circ_100964,RMVar_hsa_circ_177772,RMVar_hsa_circ_177773,RMVar_hsa_circ_177771,RMVar_hsa_circ_177769,RMVar_hsa_circ_44636 66501 RMVar_ID_66501 Human_SNP_ID_599351593 m1A Human chr16 + 29840239 29840239 29840239 AGAGCAGCTGGAACAAGGCATCCAGGATGTGTATGTGCTGTCGGAGCAGCAGGGGCTGCTGCTGA AGAGCAGCTGGAACAAGGCATCCAGGATGTGTTTGTGCTGTCGGAGCAGCAGGGGCTGCTGCTGA A T MVP Ensembl:ENSG00000013364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29840188..29840406 26863196 MeRIP-seq:(Medium) rs1260791203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22441921,Human_RBP_ID_25241495 Human_Splice_Rec_1700182,Human_Splice_Rec_1700204,Human_Splice_Rec_1700218,Human_Splice_Rec_1700266,Human_Splice_Rec_1700298 RMVar_hsa_circ_177770,RMVar_hsa_circ_104737,RMVar_hsa_circ_59024,RMVar_hsa_circ_33246,RMVar_hsa_circ_110370,RMVar_hsa_circ_328170,RMVar_hsa_circ_177768,RMVar_hsa_circ_100964,RMVar_hsa_circ_177771,RMVar_hsa_circ_12828,RMVar_hsa_circ_177769,RMVar_hsa_circ_177777,RMVar_hsa_circ_371585 66502 RMVar_ID_66502 Human_SNP_ID_599353526 m1A Human chr16 - 29846278 29846278 29846278 TCTTCTTAATGCCTCCCCCCACTCACCGTTTCAATGGCCAAGGCCTGTGCTTTTAGCTTGGCCTG TCTTCTTAATGCCTCCCCCCACTCACCGTTTCTATGGCCAAGGCCTGTGCTTTTAGCTTGGCCTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29846251..29847363 26863196 MeRIP-seq:(Medium) rs1220117453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66503 RMVar_ID_66503 Human_SNP_ID_599353527 m1A Human chr16 - 29846278 29846278 29846278 TCTTCTTAATGCCTCCCCCCACTCACCGTTTCAATGGCCAAGGCCTGTGCTTTTAGCTTGGCCTG TCTTCTTAATGCCTCCCCCCACTCACCGTTTCGATGGCCAAGGCCTGTGCTTTTAGCTTGGCCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29846251..29847363 26863196 MeRIP-seq:(Medium) rs1220117453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66504 RMVar_ID_66504 Human_SNP_ID_599353785 m1A Human chr16 + 29847270 29847270 29847270 ACTGGTCTATGCCCGGGCCCAGCTGGAGCTGGAGGTGAGCAAGGCTCAGCAGCTGGCTGAGGTGG ACTGGTCTATGCCCGGGCCCAGCTGGAGCTGGCGGTGAGCAAGGCTCAGCAGCTGGCTGAGGTGG A C MVP Ensembl:ENSG00000013364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29845923..29847989 32194978 MeRIP-seq:(Medium) rs1240338867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18983602 Human_Splice_Rec_1700194,Human_Splice_Rec_1700230 RMVar_hsa_circ_59024,RMVar_hsa_circ_100964,RMVar_hsa_circ_177769,RMVar_hsa_circ_177778,RMVar_hsa_circ_379025 66505 RMVar_ID_66505 Human_SNP_ID_599356750 m1A Human chr16 - 29858721 29858721 29858721 TCCTCTGTCCTGCCTACCCTGGTCCTGGCGGGACTTCACTATTTGACTTGGTTTCCTTTCAGATA TCCTCTGTCCTGCCTACCCTGGTCCTGGCGGGGCTTCACTATTTGACTTGGTTTCCTTTCAGATA T C CDIPT Ensembl:ENSG00000103502 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29858526..29859250 32194978 MeRIP-seq:(Medium) rs1455241376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472204,Human_RBP_ID_1003932,Human_RBP_ID_6507032,Human_RBP_ID_9061686,Human_RBP_ID_17253867,Human_RBP_ID_17369463,Human_RBP_ID_17486043,Human_RBP_ID_17875055,Human_RBP_ID_18285230,Human_RBP_ID_26445039,Human_RBP_ID_27560029 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_96910,RMVar_hsa_circ_109273,RMVar_hsa_circ_177782,RMVar_hsa_circ_86629,RMVar_hsa_circ_93954,RMVar_hsa_circ_177784,RMVar_hsa_circ_77696,RMVar_hsa_circ_177783,RMVar_hsa_circ_177780,RMVar_hsa_circ_177781 66506 RMVar_ID_66506 Human_SNP_ID_599356866 m1A Human chr16 - 29859135 29859135 29859135 CTGCCCACCTGCCCTGGGAGTCTTGCTGTGCCACACAGCTCCCCACCCCCTGCTAGGAGGTCCCA CTGCCCACCTGCCCTGGGAGTCTTGCTGTGCCGCACAGCTCCCCACCCCCTGCTAGGAGGTCCCA T C CDIPT Ensembl:ENSG00000103502 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29859085..29859269 26863196 MeRIP-seq:(Medium) rs536137149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233532,Human_RBP_ID_472221,Human_RBP_ID_1365469,Human_RBP_ID_4361954,Human_RBP_ID_27240138 Human_miRNA_ID_322234,Human_miRNA_ID_2076394,Human_miRNA_ID_2076395,Human_miRNA_ID_2076396,Human_miRNA_ID_2076397,Human_miRNA_ID_2367779,Human_miRNA_ID_2367780,Human_miRNA_ID_2367781,Human_miRNA_ID_2367782,Human_miRNA_ID_2726212,Human_miRNA_ID_2726213,Human_miRNA_ID_2726214,Human_miRNA_ID_2726215,Human_miRNA_ID_3015564,Human_miRNA_ID_3015565,Human_miRNA_ID_3015566,Human_miRNA_ID_3015567 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_96910,RMVar_hsa_circ_109273,RMVar_hsa_circ_177782,RMVar_hsa_circ_86629,RMVar_hsa_circ_93954,RMVar_hsa_circ_177784,RMVar_hsa_circ_77696,RMVar_hsa_circ_177783,RMVar_hsa_circ_177780,RMVar_hsa_circ_177781 66507 RMVar_ID_66507 Human_SNP_ID_599357240 m1A Human chr16 - 29860338 29860338 29860338 CTGCAAAGAGAAGGGACTGAAAGCGGGAAGGGAGATAAGCCAGAGAGGTCTGCAGGGCTGGAGTG CTGCAAAGAGAAGGGACTGAAAGCGGGAAGGGGGATAAGCCAGAGAGGTCTGCAGGGCTGGAGTG T C CDIPT Ensembl:ENSG00000103502 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29860336..29860449 26863196 MeRIP-seq:(Medium) rs1381268075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817299 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_96910,RMVar_hsa_circ_177782,RMVar_hsa_circ_86629,RMVar_hsa_circ_93954,RMVar_hsa_circ_177780,RMVar_hsa_circ_177781 66508 RMVar_ID_66508 Human_SNP_ID_599357509 m1A Human chr16 + 29861208 29861208 29861208 GGTACAGCAGGGCCAGGTTGACCAACAGGCACATGGTGGAGCAGCGGTCCGTCAGCATGTCCAGC GGTACAGCAGGGCCAGGTTGACCAACAGGCACGTGGTGGAGCAGCGGTCCGTCAGCATGTCCAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:29861157..29861307 32194978 MeRIP-seq:(Medium) rs763370256 Functional Loss SNV dbSNP153 33..33 33 - - - 66509 RMVar_ID_66509 Human_SNP_ID_599357902 m1A Human chr16 - 29862645 29862645 29862645 GCCCTGCTGCCCCCTCACGGCCTCCTCCTTCTACCTGCTCAGCGGCCTGCTGGACGCTTTCGATG GCCCTGCTGCCCCCTCACGGCCTCCTCCTTCTGCCTGCTCAGCGGCCTGCTGGACGCTTTCGATG T C CDIPT Ensembl:ENSG00000103502 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29862594..29863141 32194978 MeRIP-seq:(Medium) rs776673715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233535,Human_RBP_ID_1003937,Human_RBP_ID_4398592,Human_RBP_ID_20112708,Human_RBP_ID_22800883,Human_RBP_ID_26440670,Human_RBP_ID_26942378,Human_RBP_ID_27240146,Human_RBP_ID_27441171 Human_Splice_Rec_1700302,Human_Splice_Rec_1700303,Human_Splice_Rec_1700319,Human_Splice_Rec_1700340,Human_Splice_Rec_1700341,Human_Splice_Rec_1700352,Human_Splice_Rec_1700353,Human_Splice_Rec_1700362,Human_Splice_Rec_1700363,Human_Splice_Rec_1700371,Human_Splice_Rec_1700379 Human_miRNA_ID_2222925,Human_miRNA_ID_2222926,Human_miRNA_ID_2222927,Human_miRNA_ID_2222928 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_86629,RMVar_hsa_circ_177780 66510 RMVar_ID_66510 Human_SNP_ID_599358037 m1A Human chr16 - 29863000 29863000 29863000 GGTCCATGCTCCCGACGGCTGCGGGCTTCAGCATCTGGGGCCAGGTTGGGGCGGCGGGGTCCAGG GGTCCATGCTCCCGACGGCTGCGGGCTTCAGCGTCTGGGGCCAGGTTGGGGCGGCGGGGTCCAGG T C CDIPT Ensembl:ENSG00000103502 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:29862851..29863175 26863196 MeRIP-seq:(Medium) rs778007003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472243,Human_RBP_ID_817301,Human_RBP_ID_4362001,Human_RBP_ID_5464920,Human_RBP_ID_9353107,Human_RBP_ID_17653360 Human_Splice_Rec_1700317,Human_Splice_Rec_1700349 Human_miRNA_ID_2724153,Human_miRNA_ID_2724154,Human_miRNA_ID_2724155 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66511 RMVar_ID_66511 Human_SNP_ID_599358064 m1A Human chr16 - 29863043 29863043 29863043 GGCGGACTGCGCGCGCCCCCTGCGTCCCGCGCACCTCGGGGCCGGTCCATGCTCCCGACGGCTGC GGCGGACTGCGCGCGCCCCCTGCGTCCCGCGCGCCTCGGGGCCGGTCCATGCTCCCGACGGCTGC T C CDIPT Ensembl:ENSG00000103502 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29862900..29863204 26863196 MeRIP-seq:(Medium) rs1331069090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5241,Human_RBP_ID_233537,Human_RBP_ID_817302,Human_RBP_ID_893994,Human_RBP_ID_4392970,Human_RBP_ID_5142207,Human_RBP_ID_9325946,Human_RBP_ID_22441409 Human_Splice_Rec_1700317,Human_Splice_Rec_1700349 Human_miRNA_ID_2250251,Human_miRNA_ID_2250252,Human_miRNA_ID_2250253 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66512 RMVar_ID_66512 Human_SNP_ID_599360547 m1A Human chr16 + 29871654 29871654 29871654 GACCGGGTCCCGTATTTCCCTCTGCCCGAATGAGGAGGGGAGGGGCGTCCTGGGTCCTGCAGCTG GACCGGGTCCCGTATTTCCCTCTGCCCGAATGCGGAGGGGAGGGGCGTCCTGGGTCCTGCAGCTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29871551..29871704 32194978 MeRIP-seq:(Medium) rs1479973195 Functional Loss SNV dbSNP153 33..33 33 - - - 66513 RMVar_ID_66513 Human_SNP_ID_599363063 m1A Human chr16 - 29879944 29879944 29879944 AACCTTCTCGTGCCTCCCAGGATATGCCCTGGAGCCCCCTGGGCCCCCCAATGCCATCGAATGTG AACCTTCTCGTGCCTCCCAGGATATGCCCTGGGGCCCCCTGGGCCCCCCAATGCCATCGAATGTG T C SEZ6L2 Ensembl:ENSG00000174938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29878419..29879957 32194978 MeRIP-seq:(Medium) rs762585966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22760219 Human_Splice_Rec_1700419,Human_Splice_Rec_1700453,Human_Splice_Rec_1700487,Human_Splice_Rec_1700519,Human_Splice_Rec_1700551,Human_Splice_Rec_1700581 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_4491,RMVar_hsa_circ_325994,RMVar_hsa_circ_332823,RMVar_hsa_circ_177790 66514 RMVar_ID_66514 Human_SNP_ID_599368547 m1A Human chr16 + 29900701 29900697 29900701 TGAGGCCGGAGAGAAAGAAGCTGCCGCGGAGGAAGACAGGCTGCGGGTTCCCGGGACTGCAGGTC TGAGGCCGGAGAGAAAGAAGCTGCCGCGG____AGACAGGCTGCGGGTTCCCGGGACTGCAGGTC GAGGA G ASPHD1 Ensembl:ENSG00000174939 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:29900530..29901100 26863196 MeRIP-seq:(Medium) rs963303326 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4392979,Human_RBP_ID_5360070,Human_RBP_ID_9421431 Human_Splice_Rec_1700601 66515 RMVar_ID_66515 Human_SNP_ID_599368774 m1A Human chr16 + 29901342 29901342 29901342 GGGTGTTCGTGGTGGGCCTGTGGGATGCTCGGAGGCCGGCGGGCCAAGCCCAGGGGGTCCTGGGG GGGTGTTCGTGGTGGGCCTGTGGGATGCTCGGGGGCCGGCGGGCCAAGCCCAGGGGGTCCTGGGG A G ASPHD1 Ensembl:ENSG00000174939 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29901299..29901445 26863196 MeRIP-seq:(Medium) rs1466228752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8806784,Human_RBP_ID_9353109,Human_RBP_ID_9419180,Human_RBP_ID_21971221,Human_RBP_ID_22441427 RMVar_hsa_circ_177794,RMVar_hsa_circ_111687 66516 RMVar_ID_66516 Human_SNP_ID_599368820 m1A Human chr16 + 29901441 29901441 29901441 GAGCCGGCGGCTTCGGGCCTACGCAAGGCGCTACTCCTGGGCTGGGATGGGTAGAGTGAGGCGGG GAGCCGGCGGCTTCGGGCCTACGCAAGGCGCTCCTCCTGGGCTGGGATGGGTAGAGTGAGGCGGG A C ASPHD1 Ensembl:ENSG00000174939 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29901334..29901506 26863196 MeRIP-seq:(Medium) rs764642939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22760233,Human_RBP_ID_26757799 Human_miRNA_ID_2994554 RMVar_hsa_circ_177794,RMVar_hsa_circ_111687 66517 RMVar_ID_66517 Human_SNP_ID_599375207 m1A Human chr16 + 29925963 29925963 29925963 GCTTGAGACCGTAGGCGGCGGGGCCAGGCTCGAGACCCGAGGGCTTGGGGGCTTCCAGGGACGGG GCTTGAGACCGTAGGCGGCGGGGCCAGGCTCGTGACCCGAGGGCTTGGGGGCTTCCAGGGACGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29925914..29926044 32194978 MeRIP-seq:(Medium) rs1289675675 Functional Loss SNV dbSNP153 33..33 33 - - - 66518 RMVar_ID_66518 Human_SNP_ID_599375316 m1A Human chr16 + 29926169 29926169 29926169 GCGCACACGCCCACTCACCGCAGCTACTCTGCAAGACCGGCCCTCCGCCCCATCTCGCTCGCACC GCGCACACGCCCACTCACCGCAGCTACTCTGCGAGACCGGCCCTCCGCCCCATCTCGCTCGCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29925846..29926196;chr16:29925863..29926200;chr16:29925874..29926195 26863196 MeRIP-seq:(Medium) rs1267937892 Functional Loss SNV dbSNP153 33..33 33 - - - 66519 RMVar_ID_66519 Human_SNP_ID_599383738 m1A Human chr16 + 29962138 29962138 29962138 GCGCCGGCCTCCGCCCGGCCCCGAGGGGTAAGAGCGAGCGGCTGGCGGATCCGACGCGCGAGACC GCGCCGGCCTCCGCCCGGCCCCGAGGGGTAAGGGCGAGCGGCTGGCGGATCCGACGCGCGAGACC A G TMEM219 Ensembl:ENSG00000149932 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29962132..29962258 26863196 MeRIP-seq:(Medium) rs933130918 Functional Loss SNV dbSNP153 33..33 33 - - - 66520 RMVar_ID_66520 Human_SNP_ID_599384025 m1A Human chr16 + 29963166 29963166 29963166 TCTGCTCCCCATGGGCAACTGCCAGGCAGGGCACAACCTGCACCTGTGTCTGGCCCACCACCCAC TCTGCTCCCCATGGGCAACTGCCAGGCAGGGCGCAACCTGCACCTGTGTCTGGCCCACCACCCAC A G TMEM219 Ensembl:ENSG00000149932 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:29963034..29963184 32194978 MeRIP-seq:(Medium) rs780312951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472299,Human_RBP_ID_4362172,Human_RBP_ID_5113905,Human_RBP_ID_17371395 Human_Splice_Rec_1700706,Human_Splice_Rec_1700716,Human_Splice_Rec_1700726,Human_Splice_Rec_1700734,Human_Splice_Rec_1700742 Human_miRNA_ID_2381201,Human_miRNA_ID_2890905,Human_miRNA_ID_3024211,Human_miRNA_ID_3090979 RMVar_hsa_circ_320553,RMVar_hsa_circ_372944,RMVar_hsa_circ_177802 66521 RMVar_ID_66521 Human_SNP_ID_599385414 m1A Human chr16 - 29968252 29968252 29968252 AAACCCTGGCGACCCATCTGAGGCTCTTACCGAGGTGAGCAGCTTGGTCAGCACAAGGCCTTCAT AAACCCTGGCGACCCATCTGAGGCTCTTACCGTGGTGAGCAGCTTGGTCAGCACAAGGCCTTCAT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29968204..29968304 32194978 MeRIP-seq:(Medium) rs781591004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66522 RMVar_ID_66522 Human_SNP_ID_599386906 m1A Human chr16 + 29973978 29973978 29973978 CGGAGAAGAGGAGAGGCAGAGAGGGCGCGGGGACCGTCAGCAGCACCTTAGCTACAATCGTTCAG CGGAGAAGAGGAGAGGCAGAGAGGGCGCGGGGTCCGTCAGCAGCACCTTAGCTACAATCGTTCAG A T TAOK2 Ensembl:ENSG00000149930 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29973876..29974081 26863196 MeRIP-seq:(Medium) rs1229721327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46221,Human_RBP_ID_261000,Human_RBP_ID_1841200,Human_RBP_ID_4362216,Human_RBP_ID_6507166,Human_RBP_ID_8186949,Human_RBP_ID_8231061,Human_RBP_ID_8941498,Human_RBP_ID_18418712,Human_RBP_ID_22442472,Human_RBP_ID_26328867,Human_RBP_ID_27837827 66523 RMVar_ID_66523 Human_SNP_ID_599389951 m1A Human chr16 + 29985356 29985356 29985356 CGGCTGAGGGGTGAACGGGAGGAGCACAGTGCACGGCTGCAGCGGGAGCTTGAGGCGCAGCGGGC CGGCTGAGGGGTGAACGGGAGGAGCACAGTGCCCGGCTGCAGCGGGAGCTTGAGGCGCAGCGGGC A C TAOK2 Ensembl:ENSG00000149930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:29985201..29985516;chr16:29985200..29985525 26863196 MeRIP-seq:(Medium) rs967071705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817109,Human_RBP_ID_6507199,Human_RBP_ID_9372634,Human_RBP_ID_18985992 RMVar_hsa_circ_10750,RMVar_hsa_circ_81886,RMVar_hsa_circ_377391,RMVar_hsa_circ_2067,RMVar_hsa_circ_107373,RMVar_hsa_circ_177806,RMVar_hsa_circ_177807 66524 RMVar_ID_66524 Human_SNP_ID_599390104 m1A Human chr16 + 29985756 29985756 29985756 CAGCTCCAGCAGTGCCAGGCGGAGGAGGAAGCAGGGCTGCTGCGGCGGCAGCGCCAGTACTTTGA CAGCTCCAGCAGTGCCAGGCGGAGGAGGAAGCCGGGCTGCTGCGGCGGCAGCGCCAGTACTTTGA A C TAOK2 Ensembl:ENSG00000149930 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29985706..29985808 26863196 MeRIP-seq:(Medium) rs376415632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233836,Human_RBP_ID_891892,Human_RBP_ID_18985997,Human_RBP_ID_22654083,Human_RBP_ID_26329981,Human_RBP_ID_27811029 Human_Splice_Rec_1700794,Human_Splice_Rec_1700824,Human_Splice_Rec_1700856,Human_Splice_Rec_1700876,Human_Splice_Rec_1700880 RMVar_hsa_circ_10750,RMVar_hsa_circ_81886,RMVar_hsa_circ_377391,RMVar_hsa_circ_2067,RMVar_hsa_circ_107373,RMVar_hsa_circ_177806,RMVar_hsa_circ_177807,RMVar_hsa_circ_6579 66525 RMVar_ID_66525 Human_SNP_ID_599390470 m1A Human chr16 + 29986644 29986642 29986645 GGAGGCAGTCCTGGACCAAAGAATGCTTGGCGAGGAGGAGGAAGCAGTTGGAGAGAGAAGGATTC GGAGGCAGTCCTGGACCAAAGAATGCTTGGC___GAGGAGGAAGCAGTTGGAGAGAGAAGGATTC CGAG C TAOK2 Ensembl:ENSG00000149930 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29986595..29986985 26863196 MeRIP-seq:(Medium) rs747128900 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_6507203,Human_RBP_ID_12715971 RMVar_hsa_circ_107373,RMVar_hsa_circ_177807 66526 RMVar_ID_66526 Human_SNP_ID_599391238 m1A Human chr16 - 29988569 29988569 29988569 CAGGGGCCCAGACCCCAGAGCCGGTGGTGGTCATGGTGCAATGAAGCTATGAAGGCAGAGAGCAT CAGGGGCCCAGACCCCAGAGCCGGTGGTGGTCCTGGTGCAATGAAGCTATGAAGGCAGAGAGCAT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:29988471..29988603 26863196 MeRIP-seq:(Medium) rs1567252806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66527 RMVar_ID_66527 Human_SNP_ID_599392129 m1A Human chr16 - 29991310 29991310 29991310 GGAGCCAGCAGAGACGGCTGACGCCAGGCTGGAGGGGGCATGCCTGGTGGAGGAGGGCCATGGCT GGAGCCAGCAGAGACGGCTGACGCCAGGCTGGGGGGGGCATGCCTGGTGGAGGAGGGCCATGGCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:29991157..29991421 26863196 MeRIP-seq:(Medium) rs1272611681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66528 RMVar_ID_66528 Human_SNP_ID_599393168 m1A Human chr16 - 29994141 29994141 29994141 GGGTGGGAAGAGGTTGAGTGGAAGCAGCGAGGACGAGGAAGACAGTGGGAAGGGGGAACCCACAG GGGTGGGAAGAGGTTGAGTGGAAGCAGCGAGGGCGAGGAAGACAGTGGGAAGGGGGAACCCACAG T C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29994046..29994644 26863196 MeRIP-seq:(Medium) rs967815547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4362404,Human_RBP_ID_6507270,Human_RBP_ID_17067826,Human_RBP_ID_23686286,Human_RBP_ID_26328876 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66529 RMVar_ID_66529 Human_SNP_ID_599393202 m1A Human chr16 + 29994207 29994207 29994207 TAAGCTGGGTCCTGTCCTCACTCTTCCTCTGCACTGGGGGTTCTCTATCTCTCCCACTGTCATCC TAAGCTGGGTCCTGTCCTCACTCTTCCTCTGCGCTGGGGGTTCTCTATCTCTCCCACTGTCATCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:29994184..29994435 26863196 MeRIP-seq:(Medium) rs753705330 Functional Loss SNV dbSNP153 33..33 33 - - - 66530 RMVar_ID_66530 Human_SNP_ID_599393265 m1A Human chr16 + 29994335 29994335 29994335 TGGCTTTTCTGCTTACAGCTCCTCTCCTCCCTAGCTGACTTTCTCCGGCCATTGCTCCTGGTTCT TGGCTTTTCTGCTTACAGCTCCTCTCCTCCCTGGCTGACTTTCTCCGGCCATTGCTCCTGGTTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29993948..29994772 26863196 MeRIP-seq:(Medium) rs747065079 Functional Loss SNV dbSNP153 33..33 33 - - - 66531 RMVar_ID_66531 Human_SNP_ID_599393270 m1A Human chr16 - 29994346 29994346 29994346 ATTGGAAACCCAGAACCAGGAGCAATGGCCGGAGAAAGTCAGCTAGGGAGGAGAGGAGCTGTAAG ATTGGAAACCCAGAACCAGGAGCAATGGCCGGGGAAAGTCAGCTAGGGAGGAGAGGAGCTGTAAG T C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29993901..29994775 26863196 MeRIP-seq:(Medium) rs768873561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66532 RMVar_ID_66532 Human_SNP_ID_599393465 m1A Human chr16 + 29994811 29994811 29994811 TGCTGCCACCCCATTCTTTGCTGGGGGTCCAAAGTAGTCTGGGCTGGAGGCTTCAGAGCCGGACT TGCTGCCACCCCATTCTTTGCTGGGGGTCCAATGTAGTCTGGGCTGGAGGCTTCAGAGCCGGACT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29994495..29994894 32194978 MeRIP-seq:(Medium) rs1441862119 Functional Loss SNV dbSNP153 33..33 33 - - - 66533 RMVar_ID_66533 Human_SNP_ID_599393620 m1A Human chr16 - 29995175 29995175 29995175 CCGCTTCCAGGGAAGACAAACTGGACCTTACCAAGAAGGGCAAGAGGCCTCCCACCCCTTGTAGC CCGCTTCCAGGGAAGACAAACTGGACCTTACCGAGAAGGGCAAGAGGCCTCCCACCCCTTGTAGC T C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29995126..29995402 26863196 MeRIP-seq:(Medium) rs200237918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700888,Human_Splice_Rec_1700889,Human_Splice_Rec_1700900,Human_Splice_Rec_1700901,Human_Splice_Rec_1700908,Human_Splice_Rec_1700909,Human_Splice_Rec_1700919,Human_Splice_Rec_1700926 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66534 RMVar_ID_66534 Human_SNP_ID_599393844 m1A Human chr16 - 29995592 29995590 29995593 CAATCCCGGGTTGAGCAAAATGGCGCGGGAGAAGGAGATGCAGGAGTTCACCCGTAGCTTCTTCC CAATCCCGGGTTGAGCAAAATGGCGCGGGAG___GAGATGCAGGAGTTCACCCGTAGCTTCTTCC CCTT C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29995469..29995600;chr16:29995515..29995599 26863196 MeRIP-seq:(Medium) rs768150257 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1516386,Human_RBP_ID_6507275,Human_RBP_ID_17875139,Human_RBP_ID_27240224 Human_Splice_Rec_1700885,Human_Splice_Rec_1700897,Human_Splice_Rec_1700917,Human_Splice_Rec_1700921,Human_Splice_Rec_1700923,Human_Splice_Rec_1700927 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66535 RMVar_ID_66535 Human_SNP_ID_599393846 m1A Human chr16 - 29995592 29995592 29995592 CAATCCCGGGTTGAGCAAAATGGCGCGGGAGAAGGAGATGCAGGAGTTCACCCGTAGCTTCTTCC CAATCCCGGGTTGAGCAAAATGGCGCGGGAGAGGGAGATGCAGGAGTTCACCCGTAGCTTCTTCC T C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29995469..29995600;chr16:29995515..29995599 26863196 MeRIP-seq:(Medium) rs1381515532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1516386,Human_RBP_ID_6507275,Human_RBP_ID_17875139,Human_RBP_ID_27240224 Human_Splice_Rec_1700885,Human_Splice_Rec_1700897,Human_Splice_Rec_1700917,Human_Splice_Rec_1700921,Human_Splice_Rec_1700923,Human_Splice_Rec_1700927 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66536 RMVar_ID_66536 Human_SNP_ID_599394158 m1A Human chr16 - 29996288 29996288 29996288 GCCCGTTCATGACCGGCCCGGGAGTGGCGCCCAGAGTCTGCCCTCCCGCTACCCCAAGCAGTGGC GCCCGTTCATGACCGGCCCGGGAGTGGCGCCCGGAGTCTGCCCTCCCGCTACCCCAAGCAGTGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:29996226..29996452;chr16:29996226..29996426;chr16:29996141..29996437 26863196 MeRIP-seq:(Medium) rs1004591487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66537 RMVar_ID_66537 Human_SNP_ID_599394195 m1A Human chr16 + 29996352 29996352 29996352 CCGGCGGACGGCGAAGTGGACTACAAAAAAAAATACCGGAATCTGAAGCGGAAGCTCAAGTTCCT CCGGCGGACGGCGAAGTGGACTACAAAAAAAAGTACCGGAATCTGAAGCGGAAGCTCAAGTTCCT A G INO80E Ensembl:ENSG00000169592 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:29996251..29996375 26863410 MeRIP-seq:(Medium) rs1284007065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472369,Human_RBP_ID_1516394,Human_RBP_ID_1841230,Human_RBP_ID_4362520,Human_RBP_ID_17486054,Human_RBP_ID_18418713,Human_RBP_ID_18529745 Human_Splice_Rec_1700929,Human_Splice_Rec_1700939,Human_Splice_Rec_1700949,Human_Splice_Rec_1700951,Human_Splice_Rec_1700963,Human_Splice_Rec_1700979,Human_Splice_Rec_1700989,Human_Splice_Rec_1701001,Human_Splice_Rec_1701015,Human_Splice_Rec_1701027,Human_Splice_Rec_1701047,Human_Splice_Rec_1701053 66538 RMVar_ID_66538 Human_SNP_ID_599394292 m1A Human chr16 + 29996527 29996527 29996527 GGGCCCTTCACGGAGGACCGTTGGCCCAGCGCACCCCTTGCCCGTGATACAGGAGCACGAGTGCT GGGCCCTTCACGGAGGACCGTTGGCCCAGCGCCCCCCTTGCCCGTGATACAGGAGCACGAGTGCT A C INO80E Ensembl:ENSG00000169592 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:29996526..29996600 32194978 MeRIP-seq:(Medium) rs563150678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17875147,Human_RBP_ID_22199958,Human_RBP_ID_22541482 Human_Splice_Rec_1700931,Human_Splice_Rec_1700941,Human_Splice_Rec_1700953,Human_Splice_Rec_1700965,Human_Splice_Rec_1700975,Human_Splice_Rec_1700981,Human_Splice_Rec_1700991,Human_Splice_Rec_1701003,Human_Splice_Rec_1701017,Human_Splice_Rec_1701029,Human_Splice_Rec_1701049,Human_Splice_Rec_1701055 66539 RMVar_ID_66539 Human_SNP_ID_599394326 m1A Human chr16 - 29996602 29996602 29996602 CCTGCAACGTGCCTCACCTCTTGTCCCGGGACACCTTCAGTAATTTCCTTTGCGCTTTCCTCAGC CCTGCAACGTGCCTCACCTCTTGTCCCGGGACGCCTTCAGTAATTTCCTTTGCGCTTTCCTCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29996551..29996625 26863196 MeRIP-seq:(Medium) rs548456485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66540 RMVar_ID_66540 Human_SNP_ID_599394327 m1A Human chr16 - 29996602 29996602 29996602 CCTGCAACGTGCCTCACCTCTTGTCCCGGGACACCTTCAGTAATTTCCTTTGCGCTTTCCTCAGC CCTGCAACGTGCCTCACCTCTTGTCCCGGGACCCCTTCAGTAATTTCCTTTGCGCTTTCCTCAGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29996551..29996625 26863196 MeRIP-seq:(Medium) rs548456485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 66541 RMVar_ID_66541 Human_SNP_ID_62183 m1A Human chr1 - 631386 631386 631386 AGATGCAAGCAGGAGTAGGAGAGAGGGGGGTAAGAGTCAGAAGCTTATGTTGTTTATGCGGGGAA AGATGCAAGCAGGAGTAGGAGAGAGGGGGGTAGGAGTCAGAAGCTTATGTTGTTTATGCGGGGAA T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:631326..631538 26863196 MeRIP-seq:(Medium) rs1431226121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4077355 66542 RMVar_ID_66542 Human_SNP_ID_62199 m1A Human chr1 - 631397 631397 631397 TCCACTATAGCAGATGCAAGCAGGAGTAGGAGAGAGGGGGGTAAGAGTCAGAAGCTTATGTTGTT TCCACTATAGCAGATGCAAGCAGGAGTAGGAGGGAGGGGGGTAAGAGTCAGAAGCTTATGTTGTT T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:631351..631425 26863196 MeRIP-seq:(Medium) rs1227660999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4077355 66543 RMVar_ID_66543 Human_SNP_ID_62943 m1A Human chr1 - 632981 632981 632981 ATGTAAAGGATGCGTAGGGATGGGAGGGCGATAAGGACTAGGATGATGGCGGGCAGGATAGTTCA ATGTAAAGGATGCGTAGGGATGGGAGGGCGATGAGGACTAGGATGATGGCGGGCAGGATAGTTCA T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:632902..633049 26863196 MeRIP-seq:(Medium) rs4098613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4077356,Human_RBP_ID_5843547,Human_RBP_ID_17340733,Human_RBP_ID_18509609,Human_RBP_ID_18523586,Human_RBP_ID_23255425 66544 RMVar_ID_66544 Human_SNP_ID_63217 m1A Human chr1 + 633471 633471 633471 CACCCCCTCTACCCCCTCTAGAGCCCACTGTAAAGCTAACTTAGCATTAACCTTTTAAGTTAAAG CACCCCCTCTACCCCCTCTAGAGCCCACTGTAGAGCTAACTTAGCATTAACCTTTTAAGTTAAAG A G AP008439,AP008439:2,AP008439:3,AP008439:4,AP008439:5,AP008439:6,AP008439:7,AP008439:8,AP008439:9,AP008439:10,AP008439:11,trnK,AP008439:12,AP008439:13,AP008439:14,AP008439:15,AP008439:16,AP008439:17,AP008439:18,AP008439:19,AP008439:20,AP008439:21,AP008439:22,AP008439:23,AP008439:24,AP008439:25,AP008439:26,AP008439:27,AP008439:28,AP008439:29,AP008439:30,AP008439:31,AP008439:32,AP008439:33,AP008439:34,TRNK,AP008439:35,AP008439:36,AP008439:37,AP008439:38,AP008439:39,AP008439:40,AP008439:41,AP008439:42,tRNA-Lys,tRNA-lys,AP008439:43,AP008439:44,AP008439:45,AP008439:46,AP008439:47,AP008439:48,AP008439:49,AP008439:50,AP008439:51,AP008439:52,AP008439:53,TRNK:2,AP008439:54,AP008439:55,AP008439:56,AP008439:57,AP008439:58,AP008439:59,AP008439:60,AP008439:61,AP008439:62,AP008439:63,AP008439:64,AP008439:65,AP008439:66,AP008439:67,AP008439:68,AP008439:69,AP008439:70,AP008439:71 RNACentral:URS0000786016,RNACentral:URS00003B9337,RNACentral:URS00001E8760,RNACentral:URS0000206F1C,RNACentral:URS0000347FEF,RNACentral:URS0000466D15,RNACentral:URS0000ED74EC,RNACentral:URS00007879D1,RNACentral:URS0000283710,RNACentral:URS000052062D,RNACentral:URS00005C4C8B,RNACentral:URS0000148304,RNACentral:URS00003BE0FD,RNACentral:URS000058EE0E,RNACentral:URS00008D74D3,RNACentral:URS0000E1D4F6,RNACentral:URS0000DCB7B3,RNACentral:URS00004BC6B7,RNACentral:URS000041B182,RNACentral:URS0000B6662B,RNACentral:URS0000172BA5,RNACentral:URS00009E7D3B,RNACentral:URS000013F6E3,RNACentral:URS0000DC4370,RNACentral:URS00000889D7,RNACentral:URS000011830E,RNACentral:URS00004903A5,RNACentral:URS000044D4F2,RNACentral:URS0000E568C3,RNACentral:URS00005D7828,RNACentral:URS000033B98C,RNACentral:URS0000E2F126,RNACentral:URS00003C7688,RNACentral:URS0000858CDA,RNACentral:URS00005D9926,RNACentral:URS0000302167,RNACentral:URS000061CC6B,RNACentral:URS00002E6176,RNACentral:URS000073086F,RNACentral:URS000077AD1E,RNACentral:URS00007D671C,RNACentral:URS0000788D50,RNACentral:URS0000772C08,RNACentral:URS00000673A6,RNACentral:URS00001DBCFE,RNACentral:URS0000271A34,RNACentral:URS00005A8163,RNACentral:URS0000349549,RNACentral:URS00002789C4,RNACentral:URS0000772630,RNACentral:URS00004FCB4B,RNACentral:URS0000781B10,RNACentral:URS00007879B2,RNACentral:URS0000418E19,RNACentral:URS0000777407,RNACentral:URS000074DC6A,RNACentral:URS0000EE62EA,RNACentral:URS00001F4C99,RNACentral:URS00005062F6,RNACentral:URS0000ED1FE3,RNACentral:URS000049A3D7,RNACentral:URS0000460752,RNACentral:URS000029680B,RNACentral:URS0000DD5B64,RNACentral:URS000018AF6E,RNACentral:URS000000EE2E,RNACentral:URS0000DE8061,RNACentral:URS0000044942,RNACentral:URS0000DC6F45,RNACentral:URS0000479870,RNACentral:URS000020127C,RNACentral:URS00002BBA68,RNACentral:URS00005FA2B3,RNACentral:URS000029527D,RNACentral:URS00007E00D7,RNACentral:URS000006DD90 tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs564397077 Functional Loss SNV dbSNP153 33..33 33 - - - 66545 RMVar_ID_66545 Human_SNP_ID_63238 m1A Human chr1 + 633516 633515 633516 ATTAACCTTTTAAGTTAAAGATTAAGAGAACCAACACCTCTTTACAGTGAAATGCCCCAACTAAA ATTAACCTTTTAAGTTAAAGATTAAGAGAACC_ACACCTCTTTACAGTGAAATGCCCCAACTAAA CA C AP008439,AP008439:2,AP008439:3,AP008439:4,AP008439:5,AP008439:6,AP008439:7,AP008439:8,AP008439:9,AP008439:10,AP008439:11,trnK,AP008439:12,AP008439:13,AP008439:14,AP008439:15,AP008439:16,AP008439:17,AP008439:18,AP008439:19,AP008439:20,AP008439:21,AP008439:22,AP008439:23,AP008439:24,AP008439:25,AP008439:26,AP008439:27,AP008439:28,AP008439:29,AP008439:30,AP008439:31,AP008439:32,AP008439:33,AP008439:34,AP008439:35,AP008439:36,TRNK,AP008439:37,AP008439:38,AP008439:39,AP008439:40,AP008439:41,AP008439:42,AP008439:43,AP008439:44,AP008439:45,tRNA-Lys,tRNA-lys,AP008439:46,AP008439:47,AP008439:48,AP008439:49,AP008439:50,AP008439:51,AP008439:52,AP008439:53,AP008439:54,AP008439:55,AP008439:56,AP008439:57,TRNK:2,AP008439:58,AP008439:59,AP008439:60,AP008439:61,AP008439:62,AP008439:63,AP008439:64,AP008439:65,AP008439:66,AP008439:67,AP008439:68,AP008439:69,AP008439:70,AP008439:71,AP008439:72,AP008439:73,AP008439:74,AP008439:75,AP008439:76 RNACentral:URS0000786016,RNACentral:URS00003B9337,RNACentral:URS00001E8760,RNACentral:URS0000206F1C,RNACentral:URS0000347FEF,RNACentral:URS0000466D15,RNACentral:URS0000ED74EC,RNACentral:URS00007879D1,RNACentral:URS0000283710,RNACentral:URS000052062D,RNACentral:URS00005C4C8B,RNACentral:URS0000148304,RNACentral:URS00003BE0FD,RNACentral:URS0000DCC92F,RNACentral:URS000058EE0E,RNACentral:URS00008D74D3,RNACentral:URS0000E1D4F6,RNACentral:URS0000DCB7B3,RNACentral:URS00004BC6B7,RNACentral:URS000041B182,RNACentral:URS0000B6662B,RNACentral:URS0000172BA5,RNACentral:URS00009E7D3B,RNACentral:URS000013F6E3,RNACentral:URS0000DC4370,RNACentral:URS00000889D7,RNACentral:URS000011830E,RNACentral:URS00004903A5,RNACentral:URS000044D4F2,RNACentral:URS0000E568C3,RNACentral:URS0000768772,RNACentral:URS00005D7828,RNACentral:URS000033B98C,RNACentral:URS0000E2F126,RNACentral:URS00003C7688,RNACentral:URS0000858CDA,RNACentral:URS00005D9926,RNACentral:URS0000302167,RNACentral:URS000061CC6B,RNACentral:URS00002E6176,RNACentral:URS000073086F,RNACentral:URS0000EDA177,RNACentral:URS000077AD1E,RNACentral:URS00007D671C,RNACentral:URS0000788D50,RNACentral:URS0000772C08,RNACentral:URS00000673A6,RNACentral:URS00001DBCFE,RNACentral:URS0000271A34,RNACentral:URS00005A8163,RNACentral:URS0000349549,RNACentral:URS00002789C4,RNACentral:URS0000772630,RNACentral:URS00004FCB4B,RNACentral:URS0000781B10,RNACentral:URS00007879B2,RNACentral:URS0000418E19,RNACentral:URS0000DEB98F,RNACentral:URS0000777407,RNACentral:URS000074DC6A,RNACentral:URS0000EE62EA,RNACentral:URS00001F4C99,RNACentral:URS00005062F6,RNACentral:URS0000ED1FE3,RNACentral:URS000049A3D7,RNACentral:URS0000460752,RNACentral:URS000029680B,RNACentral:URS0000DD5B64,RNACentral:URS000018AF6E,RNACentral:URS000000EE2E,RNACentral:URS0000DE8061,RNACentral:URS0000044942,RNACentral:URS0000DE340F,RNACentral:URS0000DC6F45,RNACentral:URS0000479870,RNACentral:URS000020127C,RNACentral:URS00002BBA68,RNACentral:URS00005FA2B3,RNACentral:URS000029527D,RNACentral:URS00007E00D7,RNACentral:URS000006DD90 tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1269281018 Functional Loss DEL dbSNP153 33..33 33 - - - 66546 RMVar_ID_66546 Human_SNP_ID_63239 m1A Human chr1 + 633516 633516 633516 ATTAACCTTTTAAGTTAAAGATTAAGAGAACCAACACCTCTTTACAGTGAAATGCCCCAACTAAA ATTAACCTTTTAAGTTAAAGATTAAGAGAACCGACACCTCTTTACAGTGAAATGCCCCAACTAAA A G AP008439,AP008439:2,AP008439:3,AP008439:4,AP008439:5,AP008439:6,AP008439:7,AP008439:8,AP008439:9,AP008439:10,AP008439:11,trnK,AP008439:12,AP008439:13,AP008439:14,AP008439:15,AP008439:16,AP008439:17,AP008439:18,AP008439:19,AP008439:20,AP008439:21,AP008439:22,AP008439:23,AP008439:24,AP008439:25,AP008439:26,AP008439:27,AP008439:28,AP008439:29,AP008439:30,AP008439:31,AP008439:32,AP008439:33,AP008439:34,AP008439:35,AP008439:36,TRNK,AP008439:37,AP008439:38,AP008439:39,AP008439:40,AP008439:41,AP008439:42,AP008439:43,AP008439:44,AP008439:45,tRNA-Lys,tRNA-lys,AP008439:46,AP008439:47,AP008439:48,AP008439:49,AP008439:50,AP008439:51,AP008439:52,AP008439:53,AP008439:54,AP008439:55,AP008439:56,AP008439:57,TRNK:2,AP008439:58,AP008439:59,AP008439:60,AP008439:61,AP008439:62,AP008439:63,AP008439:64,AP008439:65,AP008439:66,AP008439:67,AP008439:68,AP008439:69,AP008439:70,AP008439:71,AP008439:72,AP008439:73,AP008439:74,AP008439:75,AP008439:76 RNACentral:URS0000786016,RNACentral:URS00003B9337,RNACentral:URS00001E8760,RNACentral:URS0000206F1C,RNACentral:URS0000347FEF,RNACentral:URS0000466D15,RNACentral:URS0000ED74EC,RNACentral:URS00007879D1,RNACentral:URS0000283710,RNACentral:URS000052062D,RNACentral:URS00005C4C8B,RNACentral:URS0000148304,RNACentral:URS00003BE0FD,RNACentral:URS0000DCC92F,RNACentral:URS000058EE0E,RNACentral:URS00008D74D3,RNACentral:URS0000E1D4F6,RNACentral:URS0000DCB7B3,RNACentral:URS00004BC6B7,RNACentral:URS000041B182,RNACentral:URS0000B6662B,RNACentral:URS0000172BA5,RNACentral:URS00009E7D3B,RNACentral:URS000013F6E3,RNACentral:URS0000DC4370,RNACentral:URS00000889D7,RNACentral:URS000011830E,RNACentral:URS00004903A5,RNACentral:URS000044D4F2,RNACentral:URS0000E568C3,RNACentral:URS0000768772,RNACentral:URS00005D7828,RNACentral:URS000033B98C,RNACentral:URS0000E2F126,RNACentral:URS00003C7688,RNACentral:URS0000858CDA,RNACentral:URS00005D9926,RNACentral:URS0000302167,RNACentral:URS000061CC6B,RNACentral:URS00002E6176,RNACentral:URS000073086F,RNACentral:URS0000EDA177,RNACentral:URS000077AD1E,RNACentral:URS00007D671C,RNACentral:URS0000788D50,RNACentral:URS0000772C08,RNACentral:URS00000673A6,RNACentral:URS00001DBCFE,RNACentral:URS0000271A34,RNACentral:URS00005A8163,RNACentral:URS0000349549,RNACentral:URS00002789C4,RNACentral:URS0000772630,RNACentral:URS00004FCB4B,RNACentral:URS0000781B10,RNACentral:URS00007879B2,RNACentral:URS0000418E19,RNACentral:URS0000DEB98F,RNACentral:URS0000777407,RNACentral:URS000074DC6A,RNACentral:URS0000EE62EA,RNACentral:URS00001F4C99,RNACentral:URS00005062F6,RNACentral:URS0000ED1FE3,RNACentral:URS000049A3D7,RNACentral:URS0000460752,RNACentral:URS000029680B,RNACentral:URS0000DD5B64,RNACentral:URS000018AF6E,RNACentral:URS000000EE2E,RNACentral:URS0000DE8061,RNACentral:URS0000044942,RNACentral:URS0000DE340F,RNACentral:URS0000DC6F45,RNACentral:URS0000479870,RNACentral:URS000020127C,RNACentral:URS00002BBA68,RNACentral:URS00005FA2B3,RNACentral:URS000029527D,RNACentral:URS00007E00D7,RNACentral:URS000006DD90 tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1446604054 Functional Loss SNV dbSNP153 33..33 33 - - - 66547 RMVar_ID_66547 Human_SNP_ID_63240 m1A Human chr1 + 633516 633516 633516 ATTAACCTTTTAAGTTAAAGATTAAGAGAACCAACACCTCTTTACAGTGAAATGCCCCAACTAAA ATTAACCTTTTAAGTTAAAGATTAAGAGAACCTACACCTCTTTACAGTGAAATGCCCCAACTAAA A T AP008439,AP008439:2,AP008439:3,AP008439:4,AP008439:5,AP008439:6,AP008439:7,AP008439:8,AP008439:9,AP008439:10,AP008439:11,trnK,AP008439:12,AP008439:13,AP008439:14,AP008439:15,AP008439:16,AP008439:17,AP008439:18,AP008439:19,AP008439:20,AP008439:21,AP008439:22,AP008439:23,AP008439:24,AP008439:25,AP008439:26,AP008439:27,AP008439:28,AP008439:29,AP008439:30,AP008439:31,AP008439:32,AP008439:33,AP008439:34,AP008439:35,AP008439:36,TRNK,AP008439:37,AP008439:38,AP008439:39,AP008439:40,AP008439:41,AP008439:42,AP008439:43,AP008439:44,AP008439:45,tRNA-Lys,tRNA-lys,AP008439:46,AP008439:47,AP008439:48,AP008439:49,AP008439:50,AP008439:51,AP008439:52,AP008439:53,AP008439:54,AP008439:55,AP008439:56,AP008439:57,TRNK:2,AP008439:58,AP008439:59,AP008439:60,AP008439:61,AP008439:62,AP008439:63,AP008439:64,AP008439:65,AP008439:66,AP008439:67,AP008439:68,AP008439:69,AP008439:70,AP008439:71,AP008439:72,AP008439:73,AP008439:74,AP008439:75,AP008439:76 RNACentral:URS0000786016,RNACentral:URS00003B9337,RNACentral:URS00001E8760,RNACentral:URS0000206F1C,RNACentral:URS0000347FEF,RNACentral:URS0000466D15,RNACentral:URS0000ED74EC,RNACentral:URS00007879D1,RNACentral:URS0000283710,RNACentral:URS000052062D,RNACentral:URS00005C4C8B,RNACentral:URS0000148304,RNACentral:URS00003BE0FD,RNACentral:URS0000DCC92F,RNACentral:URS000058EE0E,RNACentral:URS00008D74D3,RNACentral:URS0000E1D4F6,RNACentral:URS0000DCB7B3,RNACentral:URS00004BC6B7,RNACentral:URS000041B182,RNACentral:URS0000B6662B,RNACentral:URS0000172BA5,RNACentral:URS00009E7D3B,RNACentral:URS000013F6E3,RNACentral:URS0000DC4370,RNACentral:URS00000889D7,RNACentral:URS000011830E,RNACentral:URS00004903A5,RNACentral:URS000044D4F2,RNACentral:URS0000E568C3,RNACentral:URS0000768772,RNACentral:URS00005D7828,RNACentral:URS000033B98C,RNACentral:URS0000E2F126,RNACentral:URS00003C7688,RNACentral:URS0000858CDA,RNACentral:URS00005D9926,RNACentral:URS0000302167,RNACentral:URS000061CC6B,RNACentral:URS00002E6176,RNACentral:URS000073086F,RNACentral:URS0000EDA177,RNACentral:URS000077AD1E,RNACentral:URS00007D671C,RNACentral:URS0000788D50,RNACentral:URS0000772C08,RNACentral:URS00000673A6,RNACentral:URS00001DBCFE,RNACentral:URS0000271A34,RNACentral:URS00005A8163,RNACentral:URS0000349549,RNACentral:URS00002789C4,RNACentral:URS0000772630,RNACentral:URS00004FCB4B,RNACentral:URS0000781B10,RNACentral:URS00007879B2,RNACentral:URS0000418E19,RNACentral:URS0000DEB98F,RNACentral:URS0000777407,RNACentral:URS000074DC6A,RNACentral:URS0000EE62EA,RNACentral:URS00001F4C99,RNACentral:URS00005062F6,RNACentral:URS0000ED1FE3,RNACentral:URS000049A3D7,RNACentral:URS0000460752,RNACentral:URS000029680B,RNACentral:URS0000DD5B64,RNACentral:URS000018AF6E,RNACentral:URS000000EE2E,RNACentral:URS0000DE8061,RNACentral:URS0000044942,RNACentral:URS0000DE340F,RNACentral:URS0000DC6F45,RNACentral:URS0000479870,RNACentral:URS000020127C,RNACentral:URS00002BBA68,RNACentral:URS00005FA2B3,RNACentral:URS000029527D,RNACentral:URS00007E00D7,RNACentral:URS000006DD90 tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1446604054 Functional Loss SNV dbSNP153 33..33 33 - - - 66548 RMVar_ID_66548 Human_SNP_ID_63375 m1A Human chr1 + 633755 633755 633755 ATTGCCCCCACAATCCTAGGCCTACCCGCCGCAGTACTGATCATTCTATTTCCCCCTCTATTGAT ATTGCCCCCACAATCCTAGGCCTACCCGCCGCGGTACTGATCATTCTATTTCCCCCTCTATTGAT A G MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:633731..633823 26863410 MeRIP-seq:(Medium) rs1199097791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18198095,Human_RBP_ID_18204991 Human_miRNA_ID_1821692,Human_miRNA_ID_1852255 66549 RMVar_ID_66549 Human_SNP_ID_63606 m1A Human chr1 + 634031 634031 634031 CTAGCCATGGCCATCCCCTTATGAGCGGGCGCAGTGATTATAGGCTTTCGCTCTAAGATTAAAAA CTAGCCATGGCCATCCCCTTATGAGCGGGCGCGGTGATTATAGGCTTTCGCTCTAAGATTAAAAA A G MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:633979..634074;chr1:633916..634143;chr1:633911..634144;chr1:633976..634100;chr1:633932..634102;chr1:633976..634075;chr1:633976..634071 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs574899449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1155316,Human_RBP_ID_1432895,Human_RBP_ID_1750919,Human_RBP_ID_3317688,Human_RBP_ID_5156170,Human_RBP_ID_5843585,Human_RBP_ID_8240928,Human_RBP_ID_8315276,Human_RBP_ID_8750691,Human_RBP_ID_17182060,Human_RBP_ID_17336539,Human_RBP_ID_17754745,Human_RBP_ID_21911302,Human_RBP_ID_22488530,Human_RBP_ID_24358601 66550 RMVar_ID_66550 Human_SNP_ID_63607 m1A Human chr1 + 634031 634031 634031 CTAGCCATGGCCATCCCCTTATGAGCGGGCGCAGTGATTATAGGCTTTCGCTCTAAGATTAAAAA CTAGCCATGGCCATCCCCTTATGAGCGGGCGCTGTGATTATAGGCTTTCGCTCTAAGATTAAAAA A T MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:633979..634074;chr1:633916..634143;chr1:633911..634144;chr1:633976..634100;chr1:633932..634102;chr1:633976..634075;chr1:633976..634071 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs574899449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1155316,Human_RBP_ID_1432895,Human_RBP_ID_1750919,Human_RBP_ID_3317688,Human_RBP_ID_5156170,Human_RBP_ID_5843585,Human_RBP_ID_8240928,Human_RBP_ID_8315276,Human_RBP_ID_8750691,Human_RBP_ID_17182060,Human_RBP_ID_17336539,Human_RBP_ID_17754745,Human_RBP_ID_21911302,Human_RBP_ID_22488530,Human_RBP_ID_24358601 66551 RMVar_ID_66551 Human_SNP_ID_63618 m1A Human chr1 + 634040 634040 634040 GCCATCCCCTTATGAGCGGGCGCAGTGATTATAGGCTTTCGCTCTAAGATTAAAAATGCCCTAGC GCCATCCCCTTATGAGCGGGCGCAGTGATTATGGGCTTTCGCTCTAAGATTAAAAATGCCCTAGC A G MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:633983..634097 26863410 MeRIP-seq:(Medium) rs1238306427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1155316,Human_RBP_ID_1432897,Human_RBP_ID_1750919,Human_RBP_ID_3317688,Human_RBP_ID_5156170,Human_RBP_ID_5843586,Human_RBP_ID_8240928,Human_RBP_ID_8315277,Human_RBP_ID_17182060,Human_RBP_ID_21911302,Human_RBP_ID_24358601 66552 RMVar_ID_66552 Human_SNP_ID_63627 m1A Human chr1 - 634050 634050 634050 TAAGAAGTGGGCTAGGGCATTTTTAATCTTAGAGCGAAAGCCTATAATCACTGCGCCCGCTCATA TAAGAAGTGGGCTAGGGCATTTTTAATCTTAGGGCGAAAGCCTATAATCACTGCGCCCGCTCATA T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:633949..634125 26863410 MeRIP-seq:(Medium) rs1238379829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941,Human_RBP_ID_190720,Human_RBP_ID_4077356,Human_RBP_ID_5125014,Human_RBP_ID_5233636,Human_RBP_ID_8227656,Human_RBP_ID_8315279,Human_RBP_ID_9352335,Human_RBP_ID_17556458,Human_RBP_ID_18157915,Human_RBP_ID_18509228,Human_RBP_ID_22369317,Human_RBP_ID_22707804,Human_RBP_ID_23255221,Human_RBP_ID_24358354 66553 RMVar_ID_66553 Human_SNP_ID_63644 m1A Human chr1 + 634070 634070 634070 ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTAGCCCACTTCTTACCACAAGGCACACCTACACC ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTCGCCCACTTCTTACCACAAGGCACACCTACACC A C MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:633994..634082 26863410 MeRIP-seq:(Medium) rs530456703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072687,Human_RBP_ID_17340491 Human_miRNA_ID_1879631 66554 RMVar_ID_66554 Human_SNP_ID_63645 m1A Human chr1 + 634070 634070 634070 ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTAGCCCACTTCTTACCACAAGGCACACCTACACC ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTGGCCCACTTCTTACCACAAGGCACACCTACACC A G MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:633994..634082 26863410 MeRIP-seq:(Medium) rs530456703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072687,Human_RBP_ID_17340491 Human_miRNA_ID_1879631 66555 RMVar_ID_66555 Human_SNP_ID_63646 m1A Human chr1 + 634070 634070 634070 ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTAGCCCACTTCTTACCACAAGGCACACCTACACC ATAGGCTTTCGCTCTAAGATTAAAAATGCCCTTGCCCACTTCTTACCACAAGGCACACCTACACC A T MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:633994..634082 26863410 MeRIP-seq:(Medium) rs530456703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072687,Human_RBP_ID_17340491 Human_miRNA_ID_1879631 66556 RMVar_ID_66556 Human_SNP_ID_77164 m1A Human chr1 + 729360 729360 729360 TGGCCTAAAGAGGCCACTGGGTGGCAGGAGCTAGGTGTGTAGAAGCTGCTGAAAGGTTGGGAGCT TGGCCTAAAGAGGCCACTGGGTGGCAGGAGCTGGGTGTGTAGAAGCTGCTGAAAGGTTGGGAGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:729320..729524 26863196 MeRIP-seq:(Medium) rs75192999 Functional Loss SNV dbSNP153 33..33 33 - - - 66557 RMVar_ID_66557 Human_SNP_ID_86869 m1A Human chr1 - 778538 778538 778538 GAGTGGGGACTGGTAAGAGTGACCTCCCCGCCAGGTTCTGTGTGTTGCCGGCTGAAGAAGGGTAG GAGTGGGGACTGGTAAGAGTGACCTCCCCGCCGGGTTCTGTGTGTTGCCGGCTGAAGAAGGGTAG T C AL669831.1,AL669831.3 Ensembl:ENSG00000228327,Ensembl:ENSG00000230021 Pseudogene,Pseudogene exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:778510..778626 26863196 MeRIP-seq:(Medium) rs1413703634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744596,Human_RBP_ID_3932362,Human_RBP_ID_5538685,Human_RBP_ID_8318396,Human_RBP_ID_9552976,Human_RBP_ID_11176037,Human_RBP_ID_18158625,Human_RBP_ID_18580529,Human_RBP_ID_18964336,Human_RBP_ID_19044905,Human_RBP_ID_27797227 RMVar_hsa_circ_75663,RMVar_hsa_circ_119634,RMVar_hsa_circ_128221,RMVar_hsa_circ_128222 66558 RMVar_ID_66558 Human_SNP_ID_86893 m1A Human chr1 - 778602 778602 778602 GCGCGGGTGTTCGGCTACATCACTGGGGCGCCATGGTGCCTGGAGCTGGGCAGTTTTCTCATCAG GCGCGGGTGTTCGGCTACATCACTGGGGCGCCGTGGTGCCTGGAGCTGGGCAGTTTTCTCATCAG T C AL669831.1,AL669831.3 Ensembl:ENSG00000228327,Ensembl:ENSG00000230021 Pseudogene,Pseudogene exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:778504..778620 26863196 MeRIP-seq:(Medium) rs377318662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801288,Human_RBP_ID_5642569,Human_RBP_ID_5861355,Human_RBP_ID_18430788,Human_RBP_ID_18475729,Human_RBP_ID_18523711,Human_RBP_ID_18580531,Human_RBP_ID_18964336,Human_RBP_ID_21959330,Human_RBP_ID_27797227 RMVar_hsa_circ_75663,RMVar_hsa_circ_119634,RMVar_hsa_circ_128221,RMVar_hsa_circ_128222 66559 RMVar_ID_66559 Human_SNP_ID_89099 m1A Human chr1 + 788397 788394 788398 AGAAAGAGAGAGAGAGGGAGAGAGGGAGAGAGAAAGGAAGAGACGATGAGAGACAGAGAGAAGGA AGAAAGAGAGAGAGAGGGAGAGAGGGAGAG____AGGAAGAGACGATGAGAGACAGAGAGAAGGA GAGAA G LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:788294..788446 26863196 MeRIP-seq:(Medium) rs1418798722 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3334760,Human_RBP_ID_5091902,Human_RBP_ID_5642776 66560 RMVar_ID_66560 Human_SNP_ID_89555 m1A Human chr1 + 789344 789344 789344 GACTAGAATGGAATAGAACGGAATAGGCTCGAATGGTATGGAATGCAATGGAATGGACTCGAATG GACTAGAATGGAATAGAACGGAATAGGCTCGAGTGGTATGGAATGCAATGGAATGGACTCGAATG A G LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:789326..789391 26863196 MeRIP-seq:(Medium) rs1217765735 Functional Loss SNV dbSNP153 33..33 33 - - - 66561 RMVar_ID_66561 Human_SNP_ID_89586 m1A Human chr1 - 789403 789403 789403 GTTCCATTCGAGTCCATTACATTGCATTCCATACCATTCTAGTCTATTCTGTTCTATTCCATTCG GTTCCATTCGAGTCCATTACATTGCATTCCATTCCATTCTAGTCTATTCTGTTCTATTCCATTCG T A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:789352..789468 26863196 MeRIP-seq:(Medium) rs11240766 Functional Loss SNV dbSNP153 33..33 33 - - - 66562 RMVar_ID_66562 Human_SNP_ID_89680 m1A Human chr1 - 789568 789563 789568 AGTCCATTTCATTCCATTCCATTCCATTCCATACCATTCCATTCCATTCAATTCAAATCCACTCA AGTCCATTTCATTCCATTCCATTCCATTCCAT_____TCCATTCCATTCAATTCAAATCCACTCA AATGGT A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:789525..789672 26863196 MeRIP-seq:(Medium) rs1557540763 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_189907,Human_RBP_ID_17341258 66563 RMVar_ID_66563 Human_SNP_ID_89686 m1A Human chr1 - 789568 789568 789568 AGTCCATTTCATTCCATTCCATTCCATTCCATACCATTCCATTCCATTCAATTCAAATCCACTCA AGTCCATTTCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCAATTCAAATCCACTCA T A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:789525..789672 26863196 MeRIP-seq:(Medium) rs12747915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189907,Human_RBP_ID_17341258 66564 RMVar_ID_66564 Human_SNP_ID_89720 m1A Human chr1 + 789593 789593 789593 GGAATGGTATGGAATGGAATGGAATGGAATGAAATGGACTAGAATGGAATGGAATGGACTCGAAT GGAATGGTATGGAATGGAATGGAATGGAATGATATGGACTAGAATGGAATGGAATGGACTCGAAT A T LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789542..789642 26863196 MeRIP-seq:(Medium) rs1460865296 Functional Loss SNV dbSNP153 33..33 33 - - - 66565 RMVar_ID_66565 Human_SNP_ID_90010 m1A Human chr1 - 789860 789841 789861 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTC____________________CATCCCATTCGAGT GGAATGGAATGGAATGGACTC G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs906408227 Functional Loss DEL dbSNP153 32..51 33 - - - Human_RBP_ID_5092230 66566 RMVar_ID_66566 Human_SNP_ID_90012 m1A Human chr1 - 789860 789846 789861 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTC_______________CATTCCATCCCATTCGAGT GGAATGGAATGGACTC G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs1194952063 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_5092230 66567 RMVar_ID_66567 Human_SNP_ID_90019 m1A Human chr1 - 789860 789856 789861 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTC_____CATTCCATTCCATTCCATCCCATTCGAGT GGACTC G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs1290262092 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_5092230 66568 RMVar_ID_66568 Human_SNP_ID_90026 m1A Human chr1 - 789860 789860 789860 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTCGTGTCCATTCCATTCCATTCCATCCCATTCGAGT T A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs186823576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092230 66569 RMVar_ID_66569 Human_SNP_ID_90027 m1A Human chr1 - 789860 789860 789860 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTCGGGTCCATTCCATTCCATTCCATCCCATTCGAGT T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs186823576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092230 66570 RMVar_ID_66570 Human_SNP_ID_90302 m1A Human chr1 - 790189 790174 790189 CATTCCATTCCATTCGAGTCCATTCCATTCCAATCCTTTCGAGTCTATTCCATTCCATTCCATTC CATTCCATTCCATTCGAGTCCATTCCATTCCA_______________TTCCATTCCATTCCATTC ATAGACTCGAAAGGAT A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:790119..790245;chr1:790118..790387 26863196 MeRIP-seq:(Medium) rs1191408697 Functional Loss DEL dbSNP153 33..47 33 - - - 66571 RMVar_ID_66571 Human_SNP_ID_90305 m1A Human chr1 + 790185 790175 790185 AATGGAATGGAATGGAATGGAATAGACTCGAAAGGATTGGAATGGAATGGACTCGAATGGAATGG AATGGAATGGAATGGAATGGAAT__________GGATTGGAATGGAATGGACTCGAATGGAATGG TAGACTCGAAA T LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:790120..790230 26863196 MeRIP-seq:(Medium) rs1557541501 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_1438715,Human_RBP_ID_3334762,Human_RBP_ID_5642782,Human_RBP_ID_23411627 66572 RMVar_ID_66572 Human_SNP_ID_90319 m1A Human chr1 + 790185 790185 790185 AATGGAATGGAATGGAATGGAATAGACTCGAAAGGATTGGAATGGAATGGACTCGAATGGAATGG AATGGAATGGAATGGAATGGAATAGACTCGAACGGATTGGAATGGAATGGACTCGAATGGAATGG A C LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:790120..790230 26863196 MeRIP-seq:(Medium) rs201507278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438715,Human_RBP_ID_3334762,Human_RBP_ID_5642782,Human_RBP_ID_23411627 66573 RMVar_ID_66573 Human_SNP_ID_90320 m1A Human chr1 + 790185 790185 790185 AATGGAATGGAATGGAATGGAATAGACTCGAAAGGATTGGAATGGAATGGACTCGAATGGAATGG AATGGAATGGAATGGAATGGAATAGACTCGAATGGATTGGAATGGAATGGACTCGAATGGAATGG A T LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:790120..790230 26863196 MeRIP-seq:(Medium) rs201507278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438715,Human_RBP_ID_3334762,Human_RBP_ID_5642782,Human_RBP_ID_23411627 66574 RMVar_ID_66574 Human_SNP_ID_90323 m1A Human chr1 - 790189 790189 790189 CATTCCATTCCATTCGAGTCCATTCCATTCCAATCCTTTCGAGTCTATTCCATTCCATTCCATTC CATTCCATTCCATTCGAGTCCATTCCATTCCATTCCTTTCGAGTCTATTCCATTCCATTCCATTC T A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:790119..790245;chr1:790118..790387 26863196 MeRIP-seq:(Medium) rs146056153 Functional Loss SNV dbSNP153 33..33 33 - - - 66575 RMVar_ID_66575 Human_SNP_ID_90515 m1A Human chr1 - 790461 790461 790461 TCGAGTCCATTCCATTCCATTCCATCTGAGTCAATTCCATTCCATTCCATTCGAGTCCATTCCAT TCGAGTCCATTCCATTCCATTCCATCTGAGTCCATTCCATTCCATTCCATTCGAGTCCATTCCAT T G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:790429..790689 26863196 MeRIP-seq:(Medium) rs111203401 Functional Loss SNV dbSNP153 33..33 33 - - - 66576 RMVar_ID_66576 Human_SNP_ID_90562 m1A Human chr1 + 790509 790509 790509 GAATGGAATGGACTCGAAAGGATTGGAATGGAATACAATGGAATGGTCTCGAATGGAATGGAATG GAATGGAATGGACTCGAAAGGATTGGAATGGAGTACAATGGAATGGTCTCGAATGGAATGGAATG A G LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:790458..790697 26863196 MeRIP-seq:(Medium) rs796283072 Functional Loss SNV dbSNP153 33..33 33 - - - 66577 RMVar_ID_66577 Human_SNP_ID_90589 m1A Human chr1 + 790533 790532 790533 GGAATGGAATACAATGGAATGGTCTCGAATGGAATGGAATGGAATGGACTCGAATGGAATGGACT GGAATGGAATACAATGGAATGGTCTCGAATGG_ATGGAATGGAATGGACTCGAATGGAATGGACT GA G LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:790483..790663 26863196 MeRIP-seq:(Medium) rs1292256818 Functional Loss DEL dbSNP153 33..33 33 - - - 66578 RMVar_ID_66578 Human_SNP_ID_90590 m1A Human chr1 + 790533 790533 790533 GGAATGGAATACAATGGAATGGTCTCGAATGGAATGGAATGGAATGGACTCGAATGGAATGGACT GGAATGGAATACAATGGAATGGTCTCGAATGGCATGGAATGGAATGGACTCGAATGGAATGGACT A C LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:790483..790663 26863196 MeRIP-seq:(Medium) rs548952203 Functional Loss SNV dbSNP153 33..33 33 - - - 66579 RMVar_ID_66579 Human_SNP_ID_91015 m1A Human chr1 - 790997 790995 790998 CCATTCTATTCCATTCCATTCCATTCTATTCGAGCACCTTTCATTCCATTCCATTCCATTCCATT CCATTCTATTCCATTCCATTCCATTCTATTC___CACCTTTCATTCCATTCCATTCCATTCCATT GCTC G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:790913..791032 26863196 MeRIP-seq:(Medium) rs1352545021 Functional Loss DEL dbSNP153 32..34 33 - - - 66580 RMVar_ID_66580 Human_SNP_ID_91016 m1A Human chr1 - 790997 790997 790997 CCATTCTATTCCATTCCATTCCATTCTATTCGAGCACCTTTCATTCCATTCCATTCCATTCCATT CCATTCTATTCCATTCCATTCCATTCTATTCGTGCACCTTTCATTCCATTCCATTCCATTCCATT T A AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:790913..791032 26863196 MeRIP-seq:(Medium) rs62653114 Functional Loss SNV dbSNP153 33..33 33 - - - 66581 RMVar_ID_66581 Human_SNP_ID_91017 m1A Human chr1 - 790997 790997 790997 CCATTCTATTCCATTCCATTCCATTCTATTCGAGCACCTTTCATTCCATTCCATTCCATTCCATT CCATTCTATTCCATTCCATTCCATTCTATTCGGGCACCTTTCATTCCATTCCATTCCATTCCATT T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:790913..791032 26863196 MeRIP-seq:(Medium) rs62653114 Functional Loss SNV dbSNP153 33..33 33 - - - 66582 RMVar_ID_66582 Human_SNP_ID_91098 m1A Human chr1 + 791167 791167 791167 GGAATGCAGTTGAATTGAATGGACCCGAAAGCAATGGAATGGAATGCAATGTACTCGAATGGAAT GGAATGCAGTTGAATTGAATGGACCCGAAAGCTATGGAATGGAATGCAATGTACTCGAATGGAAT A T LINC01409 Ensembl:ENSG00000237491 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:791158..791271 26863196 MeRIP-seq:(Medium) rs1385765934 Functional Loss SNV dbSNP153 33..33 33 - - - 66583 RMVar_ID_66583 Human_SNP_ID_91272 m1A Human chr1 - 791453 791453 791453 CCATTCTATTCCATTTGAGTCCATTCCATTCCATTACATTCTAGATCATTCCATCCCAACCCATT CCATTCTATTCCATTTGAGTCCATTCCATTCCGTTACATTCTAGATCATTCCATCCCAACCCATT T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:791343..791495 26863196 MeRIP-seq:(Medium) rs1447051655 Functional Loss SNV dbSNP153 33..33 33 - - - 66584 RMVar_ID_66584 Human_SNP_ID_98246 m1A Human chr1 + 820993 820993 820993 TGCCTGCAAAGCAGATCCACCCTGTCTACACTACCTGGCTGGCCAGTAGATCCACGCTATCTACA TGCCTGCAAAGCAGATCCACCCTGTCTACACTGCCTGGCTGGCCAGTAGATCCACGCTATCTACA A G FAM87B,lnc-SAMD11-4 RNACentral:URS00008B5E4E,RNACentral:URS00008B984E lincRNA,lincRNA intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:820905..821034 26863196 MeRIP-seq:(Medium) rs1366068885 Functional Loss SNV dbSNP153 33..33 33 - - - 66585 RMVar_ID_66585 Human_SNP_ID_98450 m1A Human chr1 + 821325 821325 821325 CACACTGTCTACACTACTTGCCTGTCCAGCAGATCCACTCTGTCTACACTAACTGCCTGCCCAGC CACACTGTCTACACTACTTGCCTGTCCAGCAGTTCCACTCTGTCTACACTAACTGCCTGCCCAGC A T lnc-SAMD11-4,FAM87B,lnc-SAMD11-4:2 RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E,RNACentral:URS00008B984E lincRNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:821291..821420 26863196 MeRIP-seq:(Medium) rs1173707384 Functional Loss SNV dbSNP153 33..33 33 - - - 66586 RMVar_ID_66586 Human_SNP_ID_98738 m1A Human chr1 + 822126 822126 822126 CACTCTGTCTACACTACCTGGCTGTCCAGCAGATCCACCCTGTCTACACTACCTGCCTATCCAGC CACTCTGTCTACACTACCTGGCTGTCCAGCAGGTCCACCCTGTCTACACTACCTGCCTATCCAGC A G lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:822101..822272 26863196 MeRIP-seq:(Medium) rs1400634883 Functional Loss SNV dbSNP153 33..33 33 - - - 66587 RMVar_ID_66587 Human_SNP_ID_98870 m1A Human chr1 - 822402 822402 822402 GGCCAGGGAGGTAGTATAGACAGGGTGGGTCTACTGGACAGGGAGGTAGTATAGACAGCGTGGAT GGCCAGGGAGGTAGTATAGACAGGGTGGGTCTGCTGGACAGGGAGGTAGTATAGACAGCGTGGAT T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:822352..822903 26863196 MeRIP-seq:(Medium) rs965522274 Functional Loss SNV dbSNP153 33..33 33 - - - 66588 RMVar_ID_66588 Human_SNP_ID_98934 m1A Human chr1 + 822542 822542 822542 ATCCACCCTGTCTACACTACCTGCCTGCCCAGAAGATGCGCCATGTCTACACTACCTGCTTGTCC ATCCACCCTGTCTACACTACCTGCCTGCCCAGCAGATGCGCCATGTCTACACTACCTGCTTGTCC A C lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:822476..822589 26863196 MeRIP-seq:(Medium) rs1402578090 Functional Loss SNV dbSNP153 33..33 33 - - - 66589 RMVar_ID_66589 Human_SNP_ID_99102 m1A Human chr1 + 822829 822828 822829 CTGTCTACACTACCTGCTTGCCCAGCAGGTCCACCCTATCTACACTACCTGCCTGCCCAGCAGAT CTGTCTACACTACCTGCTTGCCCAGCAGGTCC_CCCTATCTACACTACCTGCCTGCCCAGCAGAT CA C lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:822795..822924 26863196 MeRIP-seq:(Medium) rs1474921474 Functional Loss DEL dbSNP153 33..33 33 - - - 66590 RMVar_ID_66590 Human_SNP_ID_99103 m1A Human chr1 + 822829 822829 822829 CTGTCTACACTACCTGCTTGCCCAGCAGGTCCACCCTATCTACACTACCTGCCTGCCCAGCAGAT CTGTCTACACTACCTGCTTGCCCAGCAGGTCCGCCCTATCTACACTACCTGCCTGCCCAGCAGAT A G lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:822795..822924 26863196 MeRIP-seq:(Medium) rs1404788698 Functional Loss SNV dbSNP153 33..33 33 - - - 66591 RMVar_ID_66591 Human_SNP_ID_99362 m1A Human chr1 + 823313 823313 823313 TCCGCCCTGTCTATACTACCGGCCTGTCCAGCAGATCCACTCTGTCTATACTACCTGCCTGTCCA TCCGCCCTGTCTATACTACCGGCCTGTCCAGCGGATCCACTCTGTCTATACTACCTGCCTGTCCA A G lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:822994..823393 26863196 MeRIP-seq:(Medium) rs1235564107 Functional Loss SNV dbSNP153 33..33 33 - - - 66592 RMVar_ID_66592 Human_SNP_ID_100405 m1A Human chr1 + 827316 827316 827316 GGAACCGGACACAGACGCAGATCTGGCAGCTGAGCGACAGGCTTCGGAGCATTTCCGGGCGTCGC GGAACCGGACACAGACGCAGATCTGGCAGCTGGGCGACAGGCTTCGGAGCATTTCCGGGCGTCGC A G LINC01128 Ensembl:ENSG00000228794 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:827229..827376 32194978 MeRIP-seq:(Medium) rs139039741 Functional Loss SNV dbSNP153 33..33 33 - - - 66593 RMVar_ID_66593 Human_SNP_ID_108694 m1A Human chr1 - 858569 858569 858569 TTCCAATCTCATCTCCTGCGGTTCTCCACGTGACTACCTTCCAGGCCAGCAGCCTTGTCCCGTGG TTCCAATCTCATCTCCTGCGGTTCTCCACGTGTCTACCTTCCAGGCCAGCAGCCTTGTCCCGTGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:858528..858614 26863196 MeRIP-seq:(Medium) rs528084352 Functional Loss SNV dbSNP153 33..33 33 - - - 66594 RMVar_ID_66594 Human_SNP_ID_109895 m1A Human chr1 - 862083 862083 862083 CTACCTTATCTACTATCAGCTCTCTATCATCCATCCATCATCCATCTATTTATCTACCATCTCTA CTACCTTATCTACTATCAGCTCTCTATCATCCGTCCATCATCCATCTATTTATCTACCATCTCTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:861935..862157 26863196 MeRIP-seq:(Medium) rs1278632434 Functional Loss SNV dbSNP153 33..33 33 - - - 66595 RMVar_ID_66595 Human_SNP_ID_122304 m1A Human chr1 - 904561 904517 904561 CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG CCACGTTCGGAGGAGGCCACGTTCGGAGGAGG_________________________________ GCCTCCTCCGAACGCGGCCGCCTCCTCCTCCGAACGCGGCCGCCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:904512..904705 26863196 MeRIP-seq:(Medium) rs1427969584 Functional Loss DEL dbSNP153 33..65 33 - - - 66596 RMVar_ID_66596 Human_SNP_ID_122305 m1A Human chr1 - 904561 904517 904561 CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG CCACGTTCGGAGGAGGCCACGTTCGGAGGAGG______________________AGGCGGCCGCG GCCTCCTCCGAACGCGGCCGCCTCCTCCTCCGAACGCGGCCGCCT GCCTCCTCCGAACGCGGCCGCCT - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:904512..904705 26863196 MeRIP-seq:(Medium) rs1427969584 Functional Loss DEL dbSNP153 33..54 33 - - - 66597 RMVar_ID_66597 Human_SNP_ID_122333 m1A Human chr1 - 904613 904538 904614 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGC__________________________________ CTCCTCCTCCGAACGCGGCCGCCTCCTCCTCCGAACGTGGCCTCCTCCGAACGTGGCCGCCTCCTCCTCCGAACGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs1557588899 Functional Loss DEL dbSNP153 32..65 33 - - - 66598 RMVar_ID_66598 Human_SNP_ID_122352 m1A Human chr1 - 904561 904555 904561 CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG CCACGTTCGGAGGAGGCCACGTTCGGAGGAGG______CCGCGTTCGGAGGAGGAGGCGGCCGCG GCCGCCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:904512..904705 26863196 MeRIP-seq:(Medium) rs1269883127 Functional Loss DEL dbSNP153 33..38 33 - - - 66599 RMVar_ID_66599 Human_SNP_ID_122360 m1A Human chr1 - 904613 904560 904614 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGC__________________________________ CTCCTCCTCCGAACGTGGCCTCCTCCGAACGTGGCCGCCTCCTCCTCCGAACGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs1557588936 Functional Loss DEL dbSNP153 32..65 33 - - - 66600 RMVar_ID_66600 Human_SNP_ID_122362 m1A Human chr1 - 904561 904561 904561 CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGCGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:904512..904705 26863196 MeRIP-seq:(Medium) rs1390189362 Functional Loss SNV dbSNP153 33..33 33 - - - 66601 RMVar_ID_66601 Human_SNP_ID_122395 m1A Human chr1 - 904613 904594 904613 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCC___________________GCCACGTTCGGAGG CCGCCTCCTCCTCCGAACGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs1191982678 Functional Loss DEL dbSNP153 33..51 33 - - - 66602 RMVar_ID_66602 Human_SNP_ID_122396 m1A Human chr1 - 904613 904595 904614 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGC___________________GGCCACGTTCGGAGG CGCCTCCTCCTCCGAACGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs1449687853 Functional Loss DEL dbSNP153 32..50 33 - - - 66603 RMVar_ID_66603 Human_SNP_ID_122400 m1A Human chr1 - 904613 904598 904614 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGC________________GGCGGCCACGTTCGGAGG CTCCTCCTCCGAACGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs1450963946 Functional Loss DEL dbSNP153 32..47 33 - - - 66604 RMVar_ID_66604 Human_SNP_ID_122404 m1A Human chr1 - 904613 904613 904613 GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG GGAGGAGGCGGCGGCCGCGTTCGGAGGAGGCCGCGTTCGGAGGAGGAGGCGGCCACGTTCGGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:904465..904699 26863196 MeRIP-seq:(Medium) rs370746731 Functional Loss SNV dbSNP153 33..33 33 - - - 66605 RMVar_ID_66605 Human_SNP_ID_122583 m1A Human chr1 - 904926 904906 904926 CCTCCCCGCGGCGGAGTCCGGCGACGCTCAGAACCGAATTTCCGCGGACAGATCCTCCCGGAACG CCTCCCCGCGGCGGAGTCCGGCGACGCTCAGA____________________TCCTCCCGGAACG ATCTGTCCGCGGAAATTCGGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:904875..904962 26863196 MeRIP-seq:(Medium) rs1557589175 Functional Loss DEL dbSNP153 33..52 33 - - - 66606 RMVar_ID_66606 Human_SNP_ID_122654 m1A Human chr1 - 905115 905115 905115 GGTTCCCTGGGACGCGGTGGGGCGGGGAGGGGACCCAACAGCCTCCCCCGCCACGAACGTCCCCA GGTTCCCTGGGACGCGGTGGGGCGGGGAGGGGCCCCAACAGCCTCCCCCGCCACGAACGTCCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:905106..905204 26863196 MeRIP-seq:(Medium) rs1290212644 Functional Loss SNV dbSNP153 33..33 33 - - - 66607 RMVar_ID_66607 Human_SNP_ID_122898 m1A Human chr1 + 906008 906008 906008 CCTGAACTACGGGTAGGACCCCTCTGGCCCCCAGCCCTGCCCTTGACCCGGCCCACCAAGCCCCC CCTGAACTACGGGTAGGACCCCTCTGGCCCCCCGCCCTGCCCTTGACCCGGCCCACCAAGCCCCC A C AL645608.6 Ensembl:ENSG00000272438 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:905960..906101 26863196 MeRIP-seq:(Medium) rs1234106864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5311336 66608 RMVar_ID_66608 Human_SNP_ID_123389 m1A Human chr1 + 907805 907805 907805 TCAGGAAAACTTCCCCTCCTCGGGGATCCCGCAGGGCTAAGAAACACCCTCTTCACCTCCCTCCT TCAGGAAAACTTCCCCTCCTCGGGGATCCCGCGGGGCTAAGAAACACCCTCTTCACCTCCCTCCT A G AL645608.6 Ensembl:ENSG00000272438 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:907685..908047 26863196 MeRIP-seq:(Medium) rs1292179214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8051147,Human_RBP_ID_18473022,Human_RBP_ID_18581575 66609 RMVar_ID_66609 Human_SNP_ID_123432 m1A Human chr1 + 907888 907888 907888 GCCGAGAGAGTACAGACCCTCCCCGATCTGGGAGGAGGGCCCATCACTGGCTCCCTGCCCCCTGC GCCGAGAGAGTACAGACCCTCCCCGATCTGGGTGGAGGGCCCATCACTGGCTCCCTGCCCCCTGC A T AL645608.6 Ensembl:ENSG00000272438 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:907845..908044 26863196 MeRIP-seq:(Medium) rs1180403045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18581576 66610 RMVar_ID_66610 Human_SNP_ID_123435 m1A Human chr1 - 907907 907907 907907 GTCCCGGGGGGCTTGGCGAGCAGGGGGCAGGGAGCCAGTGATGGGCCCTCCTCCCAGATCGGGGA GTCCCGGGGGGCTTGGCGAGCAGGGGGCAGGGGGCCAGTGATGGGCCCTCCTCCCAGATCGGGGA T C lnc-NOC2L-11,lnc-NOC2L-11:2,lnc-NOC2L-11:3 RNACentral:URS00009C47A9,RNACentral:URS00008BC0BE,RNACentral:URS00009C4428 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:907595..908007 26863196 MeRIP-seq:(Medium) rs1032855905 Functional Loss SNV dbSNP153 33..33 33 - - - 66611 RMVar_ID_66611 Human_SNP_ID_123598 m1A Human chr1 - 908451 908451 908451 GTATCTTTGCCTCCTCCTCCCTTTGCAGACACACTGCACACAGGCCTCTCCCAGGCCCTGCTTTC GTATCTTTGCCTCCTCCTCCCTTTGCAGACACGCTGCACACAGGCCTCTCCCAGGCCCTGCTTTC T C lnc-NOC2L-11,lnc-NOC2L-11:2,lnc-NOC2L-11:3 RNACentral:URS00009C47A9,RNACentral:URS00008B56CA,RNACentral:URS00009C4428 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:908139..908497 26863196 MeRIP-seq:(Medium) rs777319409 Functional Loss SNV dbSNP153 33..33 33 - - - 66612 RMVar_ID_66612 Human_SNP_ID_123600 m1A Human chr1 - 908453 908453 908453 CAGTATCTTTGCCTCCTCCTCCCTTTGCAGACACACTGCACACAGGCCTCTCCCAGGCCCTGCTT CAGTATCTTTGCCTCCTCCTCCCTTTGCAGACGCACTGCACACAGGCCTCTCCCAGGCCCTGCTT T C lnc-NOC2L-11,lnc-NOC2L-11:2,lnc-NOC2L-11:3 RNACentral:URS00009C47A9,RNACentral:URS00008B56CA,RNACentral:URS00009C4428 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:908231..908493;chr1:908225..908491 26863196 MeRIP-seq:(Medium) rs1333820415 Functional Loss SNV dbSNP153 33..33 33 - - - 66613 RMVar_ID_66613 Human_SNP_ID_124764 m1A Human chr1 + 911628 911628 911628 GGGTGGGCGCTAGGCAGGCAGCAGAGTGGAGAAGGTATGTCACCAGGAGAAGGGACCCAAGGAAT GGGTGGGCGCTAGGCAGGCAGCAGAGTGGAGACGGTATGTCACCAGGAGAAGGGACCCAAGGAAT A C AL645608.2,AL645608.6 Ensembl:ENSG00000230699,Ensembl:ENSG00000272438 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:911499..911744;chr1:911544..911761 26863196 MeRIP-seq:(Medium) rs371711244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2168034,Human_RBP_ID_5311339,Human_RBP_ID_5541993,Human_RBP_ID_8167428,Human_RBP_ID_22706754 66614 RMVar_ID_66614 Human_SNP_ID_127871 m1A Human chr1 - 921691 921666 921691 GTGTCCACTCCCACACACCTGTGTCCACTCCCACACCTGTGTCTCGTGTCCACTCGCTCACACCT GTGTCCACTCCCACACACCTGTGTCCACTCCC_________________________TCACACCT AGCGAGTGGACACGAGACACAGGTGT A LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D585C1,RNACentral:URS0000D5CF9D,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:921677..921806 26863196 MeRIP-seq:(Medium) rs1243326340 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_3323525,Human_RBP_ID_27401260 66615 RMVar_ID_66615 Human_SNP_ID_127889 m1A Human chr1 - 921691 921689 921692 GTGTCCACTCCCACACACCTGTGTCCACTCCCACACCTGTGTCTCGTGTCCACTCGCTCACACCT GTGTCCACTCCCACACACCTGTGTCCACTCC___ACCTGTGTCTCGTGTCCACTCGCTCACACCT TGTG T LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D585C1,RNACentral:URS0000D5CF9D,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:921677..921806 26863196 MeRIP-seq:(Medium) rs1238877283 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3323525,Human_RBP_ID_27401260 66616 RMVar_ID_66616 Human_SNP_ID_127890 m1A Human chr1 - 921691 921691 921691 GTGTCCACTCCCACACACCTGTGTCCACTCCCACACCTGTGTCTCGTGTCCACTCGCTCACACCT GTGTCCACTCCCACACACCTGTGTCCACTCCCGCACCTGTGTCTCGTGTCCACTCGCTCACACCT T C LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D585C1,RNACentral:URS0000D5CF9D,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:921677..921806 26863196 MeRIP-seq:(Medium) rs950210355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3323525,Human_RBP_ID_27401260 66617 RMVar_ID_66617 Human_SNP_ID_127918 m1A Human chr1 - 921758 921754 921758 TGTGCCCCTTCCTTGGTCCTGTCCACTCACACACACCCGTGTCCGTGTCCATGTTCACACCTGTT TGTGCCCCTTCCTTGGTCCTGTCCACTCACAC____CCGTGTCCGTGTCCATGTTCACACCTGTT GGTGT G LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D585C1,RNACentral:URS0000D5CF9D,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,exon,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:921558..921828 26863196 MeRIP-seq:(Medium) rs1048863192 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3323526,Human_RBP_ID_26870587 66618 RMVar_ID_66618 Human_SNP_ID_128714 m1A Human chr1 + 923980 923980 923980 CCGGGCGGGCGCGCGCCAGTGGACGCGGGTGCACGACTGACGCGGCCCGGGCGGCGGGGCGGGGG CCGGGCGGGCGCGCGCCAGTGGACGCGGGTGCGCGACTGACGCGGCCCGGGCGGCGGGGCGGGGG A G SAMD11 Ensembl:ENSG00000187634 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:923926..924450 26863196 MeRIP-seq:(Medium) rs1188461129 Functional Loss SNV dbSNP153 33..33 33 - - - 66619 RMVar_ID_66619 Human_SNP_ID_128752 m1A Human chr1 - 924076 924076 924076 CCGGGGCAGTCCCACGCCCGGCTCGCCGACCCACCCGCCAGGCCGAGCCCGGCAGCGAGGAGTCG CCGGGGCAGTCCCACGCCCGGCTCGCCGACCCCCCCGCCAGGCCGAGCCCGGCAGCGAGGAGTCG T G LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6,LINC02593:7 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D5B421,RNACentral:URS0000D585C1,RNACentral:URS0000D5978C,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:923926..924675 26863196 MeRIP-seq:(Medium) rs1045122792 Functional Loss SNV dbSNP153 33..33 33 - - - 66620 RMVar_ID_66620 Human_SNP_ID_128916 m1A Human chr1 - 924594 924573 924594 CGGGGCCAGCAGAGCCTCGTAACCGGCGGCCGAGGCGGGCAGCGAGGCGGCCGGGGGGAGGGCGG CGGGGCCAGCAGAGCCTCGTAACCGGCGGCCG_____________________GGGGGAGGGCGG CCGGCCGCCTCGCTGCCCGCCT C LINC02593,LINC02593:2,LINC02593:3,LINC02593:4,LINC02593:5,LINC02593:6,LINC02593:7 RNACentral:URS0000D5BCAF,RNACentral:URS0000D5B6FC,RNACentral:URS0000D5B421,RNACentral:URS0000D585C1,RNACentral:URS0000D5978C,RNACentral:URS0000D5DAD3,RNACentral:URS0000D5E1E0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:924501..924675 26863410 MeRIP-seq:(Medium) rs1015561329 Functional Loss DEL dbSNP153 33..53 33 - - - 66621 RMVar_ID_66621 Human_SNP_ID_129176 m1A Human chr1 + 925297 925297 925297 TGGGAGGGCGCGGAGCCCCGGGTTCGGGGGAGACTGGAGGGGCGCACGTGCGGCCGGGTGCGAGC TGGGAGGGCGCGGAGCCCCGGGTTCGGGGGAGCCTGGAGGGGCGCACGTGCGGCCGGGTGCGAGC A C SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:925259..925563 26863196 MeRIP-seq:(Medium) rs1156372735 Functional Loss SNV dbSNP153 33..33 33 - - - 66622 RMVar_ID_66622 Human_SNP_ID_129884 m1A Human chr1 + 926969 926969 926969 TGCTTTGGGCCTGAGGTAGGATGGGGGAGGGGATGCCCAGGGGCCTGTGAGCCATGAGTGCCGTA TGCTTTGGGCCTGAGGTAGGATGGGGGAGGGGGTGCCCAGGGGCCTGTGAGCCATGAGTGCCGTA A G SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:926961..927087 26863196 MeRIP-seq:(Medium) rs1230410999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1976,RMVar_hsa_circ_42999 66623 RMVar_ID_66623 Human_SNP_ID_131061 m1A Human chr1 + 929623 929623 929623 AGTACGGGTGGGATTGGCAGGCAGATACACGGAGGGAACGTGCGCATTTGAGTGCACGTCCACCA AGTACGGGTGGGATTGGCAGGCAGATACACGGGGGGAACGTGCGCATTTGAGTGCACGTCCACCA A G SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:929147..929763 26863196 MeRIP-seq:(Medium) rs966746323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1976,RMVar_hsa_circ_42999 66624 RMVar_ID_66624 Human_SNP_ID_131799 m1A Human chr1 + 931540 931540 931540 GGAGCTCTAAGGCGAGGGGATGTCTGCAGAGTAGAGGAACAGGGAAGGGCGTGTAGGAGGGACGA GGAGCTCTAAGGCGAGGGGATGTCTGCAGAGTGGAGGAACAGGGAAGGGCGTGTAGGAGGGACGA A G SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:931489..931979 26863196 MeRIP-seq:(Medium) rs2341361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1976,RMVar_hsa_circ_42999,RMVar_hsa_circ_128226,RMVar_hsa_circ_10092,RMVar_hsa_circ_362582,RMVar_hsa_circ_107967 66625 RMVar_ID_66625 Human_SNP_ID_131898 m1A Human chr1 + 931869 931869 931869 TTGGGGGACCCGAGTTCCTGGCTCCAGGGGGAAGCGAGTGGTAAGTCTGTGAACAGAGCCCAGCT TTGGGGGACCCGAGTTCCTGGCTCCAGGGGGATGCGAGTGGTAAGTCTGTGAACAGAGCCCAGCT A T SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:931859..931946 26863196 MeRIP-seq:(Medium) rs547823526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1976,RMVar_hsa_circ_42999,RMVar_hsa_circ_128226,RMVar_hsa_circ_10092,RMVar_hsa_circ_362582,RMVar_hsa_circ_107967 66626 RMVar_ID_66626 Human_SNP_ID_133403 m1A Human chr1 - 935655 935655 935655 GTGTGTGAGCGTGGGGATGACCTCTGAGTGCCACGTTGCTGTGCCCACGCCTCGGCATGTGGCCC GTGTGTGAGCGTGGGGATGACCTCTGAGTGCCCCGTTGCTGTGCCCACGCCTCGGCATGTGGCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:935606..935775 26863196 MeRIP-seq:(Medium) rs928636844 Functional Loss SNV dbSNP153 33..33 33 - - - 66627 RMVar_ID_66627 Human_SNP_ID_133515 m1A Human chr1 + 935822 935822 935822 CACCCTCATATCCAGCGTCCACCGCAGCCGCCACCTCGTTATGCCCGAGCATCAGAGCCGCTGTG CACCCTCATATCCAGCGTCCACCGCAGCCGCCGCCTCGTTATGCCCGAGCATCAGAGCCGCTGTG A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:935606..935983 26863196 MeRIP-seq:(Medium) rs779799519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364165 Human_Splice_Rec_790,Human_Splice_Rec_791,Human_Splice_Rec_802,Human_Splice_Rec_810,Human_Splice_Rec_811,Human_Splice_Rec_834,Human_Splice_Rec_835,Human_Splice_Rec_856,Human_Splice_Rec_857,Human_Splice_Rec_882,Human_Splice_Rec_902,Human_Splice_Rec_903,Human_Splice_Rec_926,Human_Splice_Rec_927,Human_Splice_Rec_950,Human_Splice_Rec_951,Human_Splice_Rec_988,Human_Splice_Rec_989,Human_Splice_Rec_1008,Human_Splice_Rec_1009 RMVar_hsa_circ_1976,RMVar_hsa_circ_42999,RMVar_hsa_circ_128228,RMVar_hsa_circ_21221,RMVar_hsa_circ_117075,RMVar_hsa_circ_128226,RMVar_hsa_circ_10092,RMVar_hsa_circ_362582,RMVar_hsa_circ_107967,RMVar_hsa_circ_323016,RMVar_hsa_circ_342198,RMVar_hsa_circ_374423,RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128230,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_128231,RMVar_hsa_circ_128229 66628 RMVar_ID_66628 Human_SNP_ID_134979 m1A Human chr1 - 939077 939077 939077 GCCCTCTTCTCTGAAAAGCAGTCGCTGCTGATACGGGGGGAGCGGCCCAGCCTCTTGCCCAACAG GCCCTCTTCTCTGAAAAGCAGTCGCTGCTGATGCGGGGGGAGCGGCCCAGCCTCTTGCCCAACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:939052..939393 32194978 MeRIP-seq:(Medium) rs144608636 Functional Loss SNV dbSNP153 33..33 33 - - - 66629 RMVar_ID_66629 Human_SNP_ID_135152 m1A Human chr1 + 939374 939374 939374 GTCAGCACTGAGCGAGGCCAGCACCTTTGAGGACCCTCAGCGCCTCTACCACCTGGGCCTCCCCA GTCAGCACTGAGCGAGGCCAGCACCTTTGAGGGCCCTCAGCGCCTCTACCACCTGGGCCTCCCCA A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:939324..939518 26863196 MeRIP-seq:(Medium) rs1305887367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_794,Human_Splice_Rec_814,Human_Splice_Rec_815,Human_Splice_Rec_839,Human_Splice_Rec_861,Human_Splice_Rec_906,Human_Splice_Rec_907,Human_Splice_Rec_955,Human_Splice_Rec_992,Human_Splice_Rec_993,Human_Splice_Rec_1012,Human_Splice_Rec_1013,Human_Splice_Rec_1027 RMVar_hsa_circ_1976,RMVar_hsa_circ_42999,RMVar_hsa_circ_21221,RMVar_hsa_circ_10092,RMVar_hsa_circ_362582,RMVar_hsa_circ_323016,RMVar_hsa_circ_342198,RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128230,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_128231,RMVar_hsa_circ_36297 66630 RMVar_ID_66630 Human_SNP_ID_135208 m1A Human chr1 + 939454 939454 939454 CACCCTGGCATGATCCCCCTCATCACCTCCCCAGCCACGGTGAGGACCCACCCTGGCATGATCTC CACCCTGGCATGATCCCCCTCATCACCTCCCCCGCCACGGTGAGGACCCACCCTGGCATGATCTC A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:939437..939519 26863196 MeRIP-seq:(Medium) rs1205822649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_815,Human_Splice_Rec_861,Human_Splice_Rec_907,Human_Splice_Rec_1027 RMVar_hsa_circ_1976,RMVar_hsa_circ_21221,RMVar_hsa_circ_10092,RMVar_hsa_circ_323016,RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_128231,RMVar_hsa_circ_36297 66631 RMVar_ID_66631 Human_SNP_ID_136212 m1A Human chr1 + 941466 941466 941466 AGCGTTTCGGGGGTGACACCGATCTGGGCTGCAGTGTTGAGGGCGCCACTGGGGTGCGTGAGGGA AGCGTTTCGGGGGTGACACCGATCTGGGCTGCGGTGTTGAGGGCGCCACTGGGGTGCGTGAGGGA A G SAMD11 Ensembl:ENSG00000187634 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:941462..941683 26863196 MeRIP-seq:(Medium) rs1024183997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233 66632 RMVar_ID_66632 Human_SNP_ID_136628 m1A Human chr1 - 942181 942181 942181 GGGGGCCTGAGATGGGGGCCCAGGGCGACGTGAGGGGCATTCTGCGGCGACAGCAAGGGGGGCGG GGGGGCCTGAGATGGGGGCCCAGGGCGACGTGTGGGGCATTCTGCGGCGACAGCAAGGGGGGCGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:941984..942302;chr1:942101..942300 26863196 MeRIP-seq:(Medium) rs758508950 Functional Loss SNV dbSNP153 33..33 33 - - - 66633 RMVar_ID_66633 Human_SNP_ID_136641 m1A Human chr1 + 942201 942201 942201 GCAGAATGCCCCTCACGTCGCCCTGGGCCCCCATCTCAGGCCCCCCTTCCTGGGGGTGCCCTCGG GCAGAATGCCCCTCACGTCGCCCTGGGCCCCCGTCTCAGGCCCCCCTTCCTGGGGGTGCCCTCGG A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:942151..942325 26863196 MeRIP-seq:(Medium) rs774231202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4099555 Human_Splice_Rec_818,Human_Splice_Rec_819,Human_Splice_Rec_864,Human_Splice_Rec_865,Human_Splice_Rec_884,Human_Splice_Rec_885,Human_Splice_Rec_908,Human_Splice_Rec_909,Human_Splice_Rec_932,Human_Splice_Rec_933,Human_Splice_Rec_1016,Human_Splice_Rec_1017,Human_Splice_Rec_1030,Human_Splice_Rec_1031,Human_Splice_Rec_1042,Human_Splice_Rec_1044,Human_Splice_Rec_1045,Human_Splice_Rec_1049 Human_miRNA_ID_1025550,Human_miRNA_ID_2383415,Human_miRNA_ID_2467843 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233 66634 RMVar_ID_66634 Human_SNP_ID_136646 m1A Human chr1 + 942206 942206 942206 ATGCCCCTCACGTCGCCCTGGGCCCCCATCTCAGGCCCCCCTTCCTGGGGGTGCCCTCGGCTCTG ATGCCCCTCACGTCGCCCTGGGCCCCCATCTCCGGCCCCCCTTCCTGGGGGTGCCCTCGGCTCTG A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:942101..942297;chr1:941188..942232 26863196,32194978 MeRIP-seq:(Medium) rs1011456326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4068149 Human_Splice_Rec_818,Human_Splice_Rec_819,Human_Splice_Rec_864,Human_Splice_Rec_865,Human_Splice_Rec_884,Human_Splice_Rec_885,Human_Splice_Rec_908,Human_Splice_Rec_909,Human_Splice_Rec_932,Human_Splice_Rec_933,Human_Splice_Rec_1016,Human_Splice_Rec_1017,Human_Splice_Rec_1030,Human_Splice_Rec_1031,Human_Splice_Rec_1042,Human_Splice_Rec_1044,Human_Splice_Rec_1045,Human_Splice_Rec_1049 Human_miRNA_ID_1025550,Human_miRNA_ID_2383415,Human_miRNA_ID_2467843 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233 66635 RMVar_ID_66635 Human_SNP_ID_136835 m1A Human chr1 + 942479 942479 942479 CGCCTGGCAGCAGGAGCTCCTGCGGAAGCAGAACCTGGCCCGGTAGGTGCGGGGAGGCGGGCGGG CGCCTGGCAGCAGGAGCTCCTGCGGAAGCAGAGCCTGGCCCGGTAGGTGCGGGGAGGCGGGCGGG A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:942430..942679 32194978 MeRIP-seq:(Medium) rs1412792643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_820,Human_Splice_Rec_821,Human_Splice_Rec_840,Human_Splice_Rec_841,Human_Splice_Rec_866,Human_Splice_Rec_867,Human_Splice_Rec_886,Human_Splice_Rec_887,Human_Splice_Rec_910,Human_Splice_Rec_911,Human_Splice_Rec_934,Human_Splice_Rec_935,Human_Splice_Rec_956,Human_Splice_Rec_957,Human_Splice_Rec_972,Human_Splice_Rec_973,Human_Splice_Rec_996,Human_Splice_Rec_997,Human_Splice_Rec_1018,Human_Splice_Rec_1019,Human_Splice_Rec_1032,Human_Splice_Rec_1033,Human_Splice_Rec_1046,Human_Splice_Rec_1047,Human_Splice_Rec_1050,Human_Splice_Rec_1051 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_114811,RMVar_hsa_circ_94431,RMVar_hsa_circ_128232,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233 66636 RMVar_ID_66636 Human_SNP_ID_136919 m1A Human chr1 + 942600 942600 942600 GCCCGCCGACCTCCTGCGGCAGAAGGAGCTGGAGAGCGCGCGCCCACAGCTGCTGGCGCCCGAGA GCCCGCCGACCTCCTGCGGCAGAAGGAGCTGGGGAGCGCGCGCCCACAGCTGCTGGCGCCCGAGA A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:942401..942875;chr1:942485..942615 26863196 MeRIP-seq:(Medium) rs1354615796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_822,Human_Splice_Rec_842,Human_Splice_Rec_868,Human_Splice_Rec_888,Human_Splice_Rec_912,Human_Splice_Rec_936,Human_Splice_Rec_958,Human_Splice_Rec_974,Human_Splice_Rec_998,Human_Splice_Rec_1020,Human_Splice_Rec_1034,Human_Splice_Rec_1048,Human_Splice_Rec_1052 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66637 RMVar_ID_66637 Human_SNP_ID_137014 m1A Human chr1 + 942795 942731 942795 GTCCCGGGACTCTGCCCGGCGAGCCCCCCGGAAGGGGGGTCCCGGCCCTGCCTCAGCGCGGCCCA _________________________________GGGGGGTCCCGGCCCTGCCTCAGCGCGGCCCA CAGGGGCCCCCGGGCTCCGGACCCCCCACCCCGTCCCGGGACTCTGCCCGGCGAGCCCCCCGGAA C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:942529..942850 26863196 MeRIP-seq:(Medium) rs1557610414 Functional Loss DEL dbSNP153 1..33 33 - - - Human_miRNA_ID_2571638 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66638 RMVar_ID_66638 Human_SNP_ID_137030 m1A Human chr1 + 942751 942751 942751 GCCCTGCCCCCCCAGGGGCCCCCGGGCTCCGGACCCCCCACCCCGTCCCGGGACTCTGCCCGGCG GCCCTGCCCCCCCAGGGGCCCCCGGGCTCCGGCCCCCCCACCCCGTCCCGGGACTCTGCCCGGCG A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:942701..942775 26863196 MeRIP-seq:(Medium) rs1050264682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66639 RMVar_ID_66639 Human_SNP_ID_137031 m1A Human chr1 + 942751 942751 942751 GCCCTGCCCCCCCAGGGGCCCCCGGGCTCCGGACCCCCCACCCCGTCCCGGGACTCTGCCCGGCG GCCCTGCCCCCCCAGGGGCCCCCGGGCTCCGGGCCCCCCACCCCGTCCCGGGACTCTGCCCGGCG A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:942701..942775 26863196 MeRIP-seq:(Medium) rs1050264682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66640 RMVar_ID_66640 Human_SNP_ID_137155 m1A Human chr1 + 942903 942899 942903 TGGCTCGGAAGACGAGCCCCCCAAAGACTCGGACGGAGAGGACCCCGAGACGGCAGCTGTTGGGT TGGCTCGGAAGACGAGCCCCCCAAAGACT____CGGAGAGGACCCCGAGACGGCAGCTGTTGGGT TCGGA T SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:942855..943031 26863196 MeRIP-seq:(Medium) rs1220109335 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4068239,Human_RBP_ID_11134517 Human_miRNA_ID_2569796,Human_miRNA_ID_3043563 RMVar_hsa_circ_117918,RMVar_hsa_circ_108854,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_128233,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66641 RMVar_ID_66641 Human_SNP_ID_137199 m1A Human chr1 - 942949 942949 942949 GCGCCGGCCCCTCCAGCTGGAGCTTGGCCCGGAGTGGGCCCCCTGCACCCAACAGCTGCCGTCTC GCGCCGGCCCCTCCAGCTGGAGCTTGGCCCGGGGTGGGCCCCCTGCACCCAACAGCTGCCGTCTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:942926..942975;chr1:942901..942950 26863196 MeRIP-seq:(Medium) rs764856237 Functional Loss SNV dbSNP153 33..33 33 - - - 66642 RMVar_ID_66642 Human_SNP_ID_137463 m1A Human chr1 + 943286 943286 943286 CGCGGTAGGGGGACTCTCCATGGATGGGGAGGAGGCCCCAGCCCCTGAGGACGTCACCAAGTGGA CGCGGTAGGGGGACTCTCCATGGATGGGGAGGCGGCCCCAGCCCCTGAGGACGTCACCAAGTGGA A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:942876..943369 32194978 MeRIP-seq:(Medium) rs774310110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241004 Human_Splice_Rec_824,Human_Splice_Rec_825,Human_Splice_Rec_844,Human_Splice_Rec_845,Human_Splice_Rec_870,Human_Splice_Rec_871,Human_Splice_Rec_890,Human_Splice_Rec_891,Human_Splice_Rec_914,Human_Splice_Rec_915,Human_Splice_Rec_938,Human_Splice_Rec_939,Human_Splice_Rec_960,Human_Splice_Rec_961,Human_Splice_Rec_976,Human_Splice_Rec_977,Human_Splice_Rec_1000,Human_Splice_Rec_1001,Human_Splice_Rec_1022,Human_Splice_Rec_1023,Human_Splice_Rec_1036,Human_Splice_Rec_1037 Human_miRNA_ID_2682530 RMVar_hsa_circ_117918,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66643 RMVar_ID_66643 Human_SNP_ID_137464 m1A Human chr1 + 943286 943286 943286 CGCGGTAGGGGGACTCTCCATGGATGGGGAGGAGGCCCCAGCCCCTGAGGACGTCACCAAGTGGA CGCGGTAGGGGGACTCTCCATGGATGGGGAGGGGGCCCCAGCCCCTGAGGACGTCACCAAGTGGA A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:942876..943369 32194978 MeRIP-seq:(Medium) rs774310110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241004 Human_Splice_Rec_824,Human_Splice_Rec_825,Human_Splice_Rec_844,Human_Splice_Rec_845,Human_Splice_Rec_870,Human_Splice_Rec_871,Human_Splice_Rec_890,Human_Splice_Rec_891,Human_Splice_Rec_914,Human_Splice_Rec_915,Human_Splice_Rec_938,Human_Splice_Rec_939,Human_Splice_Rec_960,Human_Splice_Rec_961,Human_Splice_Rec_976,Human_Splice_Rec_977,Human_Splice_Rec_1000,Human_Splice_Rec_1001,Human_Splice_Rec_1022,Human_Splice_Rec_1023,Human_Splice_Rec_1036,Human_Splice_Rec_1037 Human_miRNA_ID_2682530 RMVar_hsa_circ_117918,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66644 RMVar_ID_66644 Human_SNP_ID_137481 m1A Human chr1 + 943304 943304 943304 CATGGATGGGGAGGAGGCCCCAGCCCCTGAGGACGTCACCAAGTGGACCGTGGATGACGTCTGCA CATGGATGGGGAGGAGGCCCCAGCCCCTGAGGGCGTCACCAAGTGGACCGTGGATGACGTCTGCA A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:942791..943384 26863196 MeRIP-seq:(Medium) rs758278177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_824,Human_Splice_Rec_825,Human_Splice_Rec_844,Human_Splice_Rec_845,Human_Splice_Rec_870,Human_Splice_Rec_871,Human_Splice_Rec_890,Human_Splice_Rec_891,Human_Splice_Rec_914,Human_Splice_Rec_915,Human_Splice_Rec_938,Human_Splice_Rec_939,Human_Splice_Rec_960,Human_Splice_Rec_961,Human_Splice_Rec_976,Human_Splice_Rec_977,Human_Splice_Rec_1000,Human_Splice_Rec_1001,Human_Splice_Rec_1022,Human_Splice_Rec_1023,Human_Splice_Rec_1036,Human_Splice_Rec_1037 Human_miRNA_ID_2477988 RMVar_hsa_circ_117918,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66645 RMVar_ID_66645 Human_SNP_ID_137482 m1A Human chr1 + 943304 943304 943304 CATGGATGGGGAGGAGGCCCCAGCCCCTGAGGACGTCACCAAGTGGACCGTGGATGACGTCTGCA CATGGATGGGGAGGAGGCCCCAGCCCCTGAGGTCGTCACCAAGTGGACCGTGGATGACGTCTGCA A T SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:942791..943384 26863196 MeRIP-seq:(Medium) rs758278177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_824,Human_Splice_Rec_825,Human_Splice_Rec_844,Human_Splice_Rec_845,Human_Splice_Rec_870,Human_Splice_Rec_871,Human_Splice_Rec_890,Human_Splice_Rec_891,Human_Splice_Rec_914,Human_Splice_Rec_915,Human_Splice_Rec_938,Human_Splice_Rec_939,Human_Splice_Rec_960,Human_Splice_Rec_961,Human_Splice_Rec_976,Human_Splice_Rec_977,Human_Splice_Rec_1000,Human_Splice_Rec_1001,Human_Splice_Rec_1022,Human_Splice_Rec_1023,Human_Splice_Rec_1036,Human_Splice_Rec_1037 Human_miRNA_ID_2477988 RMVar_hsa_circ_117918,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66646 RMVar_ID_66646 Human_SNP_ID_137501 m1A Human chr1 + 943325 943325 943325 AGCCCCTGAGGACGTCACCAAGTGGACCGTGGATGACGTCTGCAGCTTCGTGGGGGGCCTGTCTG AGCCCCTGAGGACGTCACCAAGTGGACCGTGGGTGACGTCTGCAGCTTCGTGGGGGGCCTGTCTG A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:943301..943350 26863196 MeRIP-seq:(Medium) rs1342687947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11134921 Human_Splice_Rec_824,Human_Splice_Rec_825,Human_Splice_Rec_844,Human_Splice_Rec_845,Human_Splice_Rec_870,Human_Splice_Rec_871,Human_Splice_Rec_890,Human_Splice_Rec_891,Human_Splice_Rec_914,Human_Splice_Rec_915,Human_Splice_Rec_938,Human_Splice_Rec_939,Human_Splice_Rec_960,Human_Splice_Rec_961,Human_Splice_Rec_976,Human_Splice_Rec_977,Human_Splice_Rec_1000,Human_Splice_Rec_1001,Human_Splice_Rec_1022,Human_Splice_Rec_1023,Human_Splice_Rec_1036,Human_Splice_Rec_1037 RMVar_hsa_circ_117918,RMVar_hsa_circ_94431,RMVar_hsa_circ_128234,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66647 RMVar_ID_66647 Human_SNP_ID_137531 m1A Human chr1 - 943360 943360 943360 GGGGCCCCCCCTTACCCGAGTGTACTCTCCACAGCCAGACAGGCCCCCCACGAAGCTGCAGACGT GGGGCCCCCCCTTACCCGAGTGTACTCTCCACTGCCAGACAGGCCCCCCACGAAGCTGCAGACGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:943184..943825 26863196 MeRIP-seq:(Medium) rs1214532268 Functional Loss SNV dbSNP153 33..33 33 - - - 66648 RMVar_ID_66648 Human_SNP_ID_137532 m1A Human chr1 - 943360 943360 943360 GGGGCCCCCCCTTACCCGAGTGTACTCTCCACAGCCAGACAGGCCCCCCACGAAGCTGCAGACGT GGGGCCCCCCCTTACCCGAGTGTACTCTCCACCGCCAGACAGGCCCCCCACGAAGCTGCAGACGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:943184..943825 26863196 MeRIP-seq:(Medium) rs1214532268 Functional Loss SNV dbSNP153 33..33 33 - - - 66649 RMVar_ID_66649 Human_SNP_ID_137828 m1A Human chr1 + 943736 943736 943736 AGGGAGCAGGGGATCGACGGGGAGACCCTGCCACTGCTGACGGAGGAGCACCTGCTGACCAACAT AGGGAGCAGGGGATCGACGGGGAGACCCTGCCGCTGCTGACGGAGGAGCACCTGCTGACCAACAT A G SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:943701..943825 26863196 MeRIP-seq:(Medium) rs1196946601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4068250,Human_RBP_ID_5875592,Human_RBP_ID_17759779 Human_Splice_Rec_826,Human_Splice_Rec_827,Human_Splice_Rec_846,Human_Splice_Rec_847,Human_Splice_Rec_872,Human_Splice_Rec_873,Human_Splice_Rec_892,Human_Splice_Rec_893,Human_Splice_Rec_916,Human_Splice_Rec_917,Human_Splice_Rec_940,Human_Splice_Rec_941,Human_Splice_Rec_962,Human_Splice_Rec_963,Human_Splice_Rec_978,Human_Splice_Rec_979,Human_Splice_Rec_1002,Human_Splice_Rec_1003,Human_Splice_Rec_1024,Human_Splice_Rec_1025,Human_Splice_Rec_1038 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235,RMVar_hsa_circ_84175,RMVar_hsa_circ_128236 66650 RMVar_ID_66650 Human_SNP_ID_138086 m1A Human chr1 + 944031 944029 944031 AACTCGGCACAGGAGAGCAGCCCTTGTCCCCCACGACGGCCACGTCCCCCTATGGAGGGGGCCAC AACTCGGCACAGGAGAGCAGCCCTTGTCCCC__CGACGGCCACGTCCCCCTATGGAGGGGGCCAC CCA C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:943909..944101 26863196 MeRIP-seq:(Medium) rs1401811443 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_364529,Human_RBP_ID_4099590,Human_RBP_ID_22147819,Human_RBP_ID_27401381 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 66651 RMVar_ID_66651 Human_SNP_ID_138089 m1A Human chr1 + 944031 944031 944031 AACTCGGCACAGGAGAGCAGCCCTTGTCCCCCACGACGGCCACGTCCCCCTATGGAGGGGGCCAC AACTCGGCACAGGAGAGCAGCCCTTGTCCCCCCCGACGGCCACGTCCCCCTATGGAGGGGGCCAC A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:943909..944101 26863196 MeRIP-seq:(Medium) rs890732763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364529,Human_RBP_ID_4099590,Human_RBP_ID_22147819,Human_RBP_ID_27401381 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 66652 RMVar_ID_66652 Human_SNP_ID_138099 m1A Human chr1 + 944040 944040 944040 CAGGAGAGCAGCCCTTGTCCCCCACGACGGCCACGTCCCCCTATGGAGGGGGCCACGCCCTTGCC CAGGAGAGCAGCCCTTGTCCCCCACGACGGCCCCGTCCCCCTATGGAGGGGGCCACGCCCTTGCC A C SAMD11 Ensembl:ENSG00000187634 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:943901..944083 26863196 MeRIP-seq:(Medium) rs753495417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4068258,Human_RBP_ID_22147819 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 66653 RMVar_ID_66653 Human_SNP_ID_138319 m1A Human chr1 - 944307 944307 944307 CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGAAAATTTGTTCCTTTCCTTTGAAGTCACATTTT CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGGAAATTTGTTCCTTTCCTTTGAAGTCACATTTT T C NOC2L Ensembl:ENSG00000188976 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5875742,Human_RBP_ID_21999013,Human_RBP_ID_22786394,Human_RBP_ID_27401387 GWAS_ID_7965,GWAS_ID_7966 66654 RMVar_ID_66654 Human_SNP_ID_138320 m1A Human chr1 - 944307 944307 944307 CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGAAAATTTGTTCCTTTCCTTTGAAGTCACATTTT CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGCAAATTTGTTCCTTTCCTTTGAAGTCACATTTT T G NOC2L Ensembl:ENSG00000188976 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5875742,Human_RBP_ID_21999013,Human_RBP_ID_22786394,Human_RBP_ID_27401387 GWAS_ID_7965,GWAS_ID_7966 66655 RMVar_ID_66655 Human_SNP_ID_138520 m1A Human chr1 + 944626 944622 944626 CCCAACTGCACAGACGCCAGCCTCTAGGCCTGACTGCCAGGGAGGTGGAAACACTGGCCACCAGC CCCAACTGCACAGACGCCAGCCTCTAGGC____CTGCCAGGGAGGTGGAAACACTGGCCACCAGC CCTGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:944576..944625 26863196 MeRIP-seq:(Medium) rs1396999215 Functional Loss DEL dbSNP153 30..33 33 - - - 66656 RMVar_ID_66656 Human_SNP_ID_138599 m1A Human chr1 - 944728 944728 944728 GCTGCAGCAGCTGGCCCAGGGGCCGGAGGACGAGCTGGAGGATCTGCAGCTCTCAGAGGACGACT GCTGCAGCAGCTGGCCCAGGGGCCGGAGGACGGGCTGGAGGATCTGCAGCTCTCAGAGGACGACT T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:944309..944825;chr1:944397..944825 26863196 MeRIP-seq:(Medium) rs1278053687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5875789,Human_RBP_ID_17759818,Human_RBP_ID_18582319,Human_RBP_ID_22426790,Human_RBP_ID_27799522 Human_Splice_Rec_1088,Human_Splice_Rec_1096,Human_Splice_Rec_1128 66657 RMVar_ID_66657 Human_SNP_ID_138868 m1A Human chr1 - 945109 945097 945109 CTGAGGCCCCTGAGCACTCGGCATGGGGTGGAAGACGATGAAGAGGACGAGGAGGAGGGCGAGGA CTGAGGCCCCTGAGCACTCGGCATGGGGTGGA____________GGACGAGGAGGAGGGCGAGGA CTCTTCATCGTCT C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:945026..945166;chr1:945001..945153 26863196 MeRIP-seq:(Medium) rs752411686 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_364549,Human_RBP_ID_853348,Human_RBP_ID_1755696,Human_RBP_ID_3324429,Human_RBP_ID_3934742,Human_RBP_ID_4068298,Human_RBP_ID_5086073,Human_RBP_ID_5538095,Human_RBP_ID_5875810,Human_RBP_ID_8753401,Human_RBP_ID_8976549,Human_RBP_ID_9269486,Human_RBP_ID_18582321,Human_RBP_ID_22425968,Human_RBP_ID_22426792,Human_RBP_ID_24734381,Human_RBP_ID_26309928 Human_Splice_Rec_1086,Human_Splice_Rec_1087,Human_Splice_Rec_1094,Human_Splice_Rec_1095,Human_Splice_Rec_1126,Human_Splice_Rec_1127 RMVar_hsa_circ_120244,RMVar_hsa_circ_128237 66658 RMVar_ID_66658 Human_SNP_ID_138869 m1A Human chr1 - 945109 945097 945109 CTGAGGCCCCTGAGCACTCGGCATGGGGTGGAAGACGATGAAGAGGACGAGGAGGAGGGCGAGGA CTGAGGCCCCTGAGCACTCGGCATGGGGTGGA_________AGAGGACGAGGAGGAGGGCGAGGA CTCTTCATCGTCT CTCT NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:945026..945166;chr1:945001..945153 26863196 MeRIP-seq:(Medium) rs752411686 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_364549,Human_RBP_ID_853348,Human_RBP_ID_1755696,Human_RBP_ID_3324429,Human_RBP_ID_3934742,Human_RBP_ID_4068298,Human_RBP_ID_5086073,Human_RBP_ID_5538095,Human_RBP_ID_5875810,Human_RBP_ID_8753401,Human_RBP_ID_8976549,Human_RBP_ID_9269486,Human_RBP_ID_18582321,Human_RBP_ID_22425968,Human_RBP_ID_22426792,Human_RBP_ID_24734381,Human_RBP_ID_26309928 Human_Splice_Rec_1086,Human_Splice_Rec_1087,Human_Splice_Rec_1094,Human_Splice_Rec_1095,Human_Splice_Rec_1126,Human_Splice_Rec_1127 RMVar_hsa_circ_120244,RMVar_hsa_circ_128237 66659 RMVar_ID_66659 Human_SNP_ID_139049 m1A Human chr1 + 945485 945485 945485 CTCTGGGAAGTCCAGCAGAGCCCTCCAGGCCCACCCTTCCCCTGGGAGCACCACGCAGGCCCCAC CTCTGGGAAGTCCAGCAGAGCCCTCCAGGCCCGCCCTTCCCCTGGGAGCACCACGCAGGCCCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:945479..945657;chr1:945479..945675 26863196 MeRIP-seq:(Medium) rs199968983 Functional Loss SNV dbSNP153 33..33 33 - - - 66660 RMVar_ID_66660 Human_SNP_ID_139060 m1A Human chr1 - 945495 945495 945495 TCGGAGAGAGGTGGGGCCTGCGTGGTGCTCCCAGGGGAAGGGTGGGCCTGGAGGGCTCTGCTGGA TCGGAGAGAGGTGGGGCCTGCGTGGTGCTCCCCGGGGAAGGGTGGGCCTGGAGGGCTCTGCTGGA T G NOC2L Ensembl:ENSG00000188976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:945491..945675 26863196 MeRIP-seq:(Medium) rs57556460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853349,Human_RBP_ID_9357775,Human_RBP_ID_19033452,Human_RBP_ID_22635880 66661 RMVar_ID_66661 Human_SNP_ID_141953 m1A Human chr1 - 952102 952102 952102 ATACCAGTCTGTGTACAACTGGCAGTATGTGCACTGCCTCTTCCTGTGGTGCCGGGTCCTGAGCA ATACCAGTCTGTGTACAACTGGCAGTATGTGCTCTGCCTCTTCCTGTGGTGCCGGGTCCTGAGCA T A NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:952051..952474 32194978 MeRIP-seq:(Medium) rs774290521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364561,Human_RBP_ID_4068329,Human_RBP_ID_8320862,Human_RBP_ID_17759843,Human_RBP_ID_22426795 Human_Splice_Rec_1072,Human_Splice_Rec_1112 Human_miRNA_ID_2054351,Human_miRNA_ID_2077345,Human_miRNA_ID_2079671,Human_miRNA_ID_2090211,Human_miRNA_ID_2278664,Human_miRNA_ID_2456028,Human_miRNA_ID_2458726,Human_miRNA_ID_2460936,Human_miRNA_ID_2633594,Human_miRNA_ID_2636281,Human_miRNA_ID_2638974 RMVar_hsa_circ_4241,RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243 66662 RMVar_ID_66662 Human_SNP_ID_142066 m1A Human chr1 + 952381 952381 952381 GTCGGGCACCTGGGCTGCCCCACCCCATGCCCAGCATGAGCCTGGAAGGGCCCCACCACACACCT GTCGGGCACCTGGGCTGCCCCACCCCATGCCCTGCATGAGCCTGGAAGGGCCCCACCACACACCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:952379..952527 26863196 MeRIP-seq:(Medium) rs1342989947 Functional Loss SNV dbSNP153 33..33 33 - - - 66663 RMVar_ID_66663 Human_SNP_ID_142464 m1A Human chr1 - 953259 953259 953259 CAGAGAATGGTGATCGTATGGAGCACTGGGGAAGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT CAGAGAATGGTGATCGTATGGAGCACTGGGGAGGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3748596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223048,Human_RBP_ID_8754549,Human_RBP_ID_18966604 Human_Splice_Rec_1068,Human_Splice_Rec_1069,Human_Splice_Rec_1108,Human_Splice_Rec_1109 Human_miRNA_ID_2255883 GWAS_ID_7967,GWAS_ID_7968 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243 66664 RMVar_ID_66664 Human_SNP_ID_142465 m1A Human chr1 - 953259 953259 953259 CAGAGAATGGTGATCGTATGGAGCACTGGGGAAGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT CAGAGAATGGTGATCGTATGGAGCACTGGGGACGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT T G NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3748596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223048,Human_RBP_ID_8754549,Human_RBP_ID_18966604 Human_Splice_Rec_1068,Human_Splice_Rec_1069,Human_Splice_Rec_1108,Human_Splice_Rec_1109 Human_miRNA_ID_2255883 GWAS_ID_7967,GWAS_ID_7968 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243 66665 RMVar_ID_66665 Human_SNP_ID_142974 m1A Human chr1 + 954270 954270 954270 GGACAGACACAGGGGCTTAGGAGGACCCTCTCAAGTGCATTAGCTCCTCCTTCAGTGGCCTTGAA GGACAGACACAGGGGCTTAGGAGGACCCTCTCTAGTGCATTAGCTCCTCCTTCAGTGGCCTTGAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:954267..954386 26863196 MeRIP-seq:(Medium) rs1242628373 Functional Loss SNV dbSNP153 33..33 33 - - - 66666 RMVar_ID_66666 Human_SNP_ID_143227 m1A Human chr1 + 955006 954999 955006 CCTCACACCTGTGCTGACACTGGCTGCTGGGCACCTGCAGCTGCCCACCCAGACCCAGGAGGCAG CCTCACACCTGTGCTGACACTGGCTG_______CCTGCAGCTGCCCACCCAGACCCAGGAGGCAG GCTGGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:955002..955102 26863196 MeRIP-seq:(Medium) rs1326172780 Functional Loss DEL dbSNP153 27..33 33 - - - 66667 RMVar_ID_66667 Human_SNP_ID_143508 m1A Human chr1 - 955777 955777 955777 TCTTGGGGACCCTGAGAAGGCAGCGGGGCACGAGGGACCGTTGGGAGAGGCTGGGCACTTGGGGC TCTTGGGGACCCTGAGAAGGCAGCGGGGCACGGGGGACCGTTGGGAGAGGCTGGGCACTTGGGGC T C NOC2L Ensembl:ENSG00000188976 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:955775..955918 26863196 MeRIP-seq:(Medium) rs553088739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804222,Human_RBP_ID_17098893,Human_RBP_ID_23255430 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239 66668 RMVar_ID_66668 Human_SNP_ID_143706 m1A Human chr1 - 956155 956155 956155 AAGTGGTACAGGCGTTCCGAGCAGCTGTGGCCACCACCCGAGGGGACCAGGAAAGTGCTGAGGCC AAGTGGTACAGGCGTTCCGAGCAGCTGTGGCCGCCACCCGAGGGGACCAGGAAAGTGCTGAGGCC T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:956151..956200 26863196 MeRIP-seq:(Medium) rs1169166328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_980272,Human_RBP_ID_3932376,Human_RBP_ID_8752591,Human_RBP_ID_9269497,Human_RBP_ID_17759854,Human_RBP_ID_22430129,Human_RBP_ID_27401404 Human_Splice_Rec_1060,Human_Splice_Rec_1061,Human_Splice_Rec_1100,Human_Splice_Rec_1101,Human_Splice_Rec_1138,Human_Splice_Rec_1139 Human_miRNA_ID_2673710,Human_miRNA_ID_2924467 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_26366,RMVar_hsa_circ_95178,RMVar_hsa_circ_128247 66669 RMVar_ID_66669 Human_SNP_ID_144018 m1A Human chr1 - 956932 956932 956932 GGCTGAAGGGGAAGAAGAATTCTGTTCCTGTGACCGTCGCCATGGTTGAGAGATGGAAGCAGGCA GGCTGAAGGGGAAGAAGAATTCTGTTCCTGTGCCCGTCGCCATGGTTGAGAGATGGAAGCAGGCA T G NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1399599086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273403,Human_RBP_ID_364596,Human_RBP_ID_851050,Human_RBP_ID_1436316,Human_RBP_ID_3932379,Human_RBP_ID_4068423,Human_RBP_ID_5109338,Human_RBP_ID_5332436,Human_RBP_ID_8320952,Human_RBP_ID_8752602,Human_RBP_ID_8976623,Human_RBP_ID_9269498,Human_RBP_ID_9342456,Human_RBP_ID_9355280,Human_RBP_ID_11137932,Human_RBP_ID_17763252,Human_RBP_ID_18964343,Human_RBP_ID_24541752,Human_RBP_ID_26309603 Human_Splice_Rec_1058,Human_Splice_Rec_1059,Human_Splice_Rec_1098,Human_Splice_Rec_1099,Human_Splice_Rec_1136,Human_Splice_Rec_1137 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 66670 RMVar_ID_66670 Human_SNP_ID_144053 m1A Human chr1 - 956993 956992 956993 GAAGCCAGTGAGGAGGAGGATGGAGCGGAGGAAGGAGAAGATGGGGACAGAGTCCCCAGAGGGCT GAAGCCAGTGAGGAGGAGGATGGAGCGGAGGA_GGAGAAGATGGGGACAGAGTCCCCAGAGGGCT CT C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:956876..957263;chr1:956876..957175;chr1:956900..957175 26863196 MeRIP-seq:(Medium) rs1557623173 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3932380,Human_RBP_ID_4068446,Human_RBP_ID_5330929,Human_RBP_ID_8754554,Human_RBP_ID_9269499,Human_RBP_ID_17762269,Human_RBP_ID_18964344,Human_RBP_ID_19042457,Human_RBP_ID_22426797,Human_RBP_ID_22734461,Human_RBP_ID_22786414,Human_RBP_ID_24541752,Human_RBP_ID_24735344,Human_RBP_ID_26309935 Human_Splice_Rec_1058,Human_Splice_Rec_1059,Human_Splice_Rec_1098,Human_Splice_Rec_1099,Human_Splice_Rec_1136,Human_Splice_Rec_1137 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 66671 RMVar_ID_66671 Human_SNP_ID_144055 m1A Human chr1 - 956997 956997 956997 GCAGGAAGCCAGTGAGGAGGAGGATGGAGCGGAGGAAGGAGAAGATGGGGACAGAGTCCCCAGAG GCAGGAAGCCAGTGAGGAGGAGGATGGAGCGGGGGAAGGAGAAGATGGGGACAGAGTCCCCAGAG T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:956894..957274 26863196 MeRIP-seq:(Medium) rs1387564328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932380,Human_RBP_ID_5330929,Human_RBP_ID_5876754,Human_RBP_ID_8754554,Human_RBP_ID_9269499,Human_RBP_ID_17759915,Human_RBP_ID_18964344,Human_RBP_ID_19042457,Human_RBP_ID_22426797,Human_RBP_ID_22734461,Human_RBP_ID_22786414,Human_RBP_ID_24541752,Human_RBP_ID_24735344,Human_RBP_ID_26309935 Human_Splice_Rec_1058,Human_Splice_Rec_1098,Human_Splice_Rec_1136 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 66672 RMVar_ID_66672 Human_SNP_ID_144056 m1A Human chr1 - 956997 956997 956997 GCAGGAAGCCAGTGAGGAGGAGGATGGAGCGGAGGAAGGAGAAGATGGGGACAGAGTCCCCAGAG GCAGGAAGCCAGTGAGGAGGAGGATGGAGCGGCGGAAGGAGAAGATGGGGACAGAGTCCCCAGAG T G NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:956894..957274 26863196 MeRIP-seq:(Medium) rs1387564328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932380,Human_RBP_ID_5330929,Human_RBP_ID_5876754,Human_RBP_ID_8754554,Human_RBP_ID_9269499,Human_RBP_ID_17759915,Human_RBP_ID_18964344,Human_RBP_ID_19042457,Human_RBP_ID_22426797,Human_RBP_ID_22734461,Human_RBP_ID_22786414,Human_RBP_ID_24541752,Human_RBP_ID_24735344,Human_RBP_ID_26309935 Human_Splice_Rec_1058,Human_Splice_Rec_1098,Human_Splice_Rec_1136 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 66673 RMVar_ID_66673 Human_SNP_ID_144072 m1A Human chr1 - 957024 957024 957024 CACTCTCCTTCAGCTCAGCCTTTCTGTGCAGGAAGCCAGTGAGGAGGAGGATGGAGCGGAGGAAG CACTCTCCTTCAGCTCAGCCTTTCTGTGCAGGCAGCCAGTGAGGAGGAGGATGGAGCGGAGGAAG T G NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:957007..957180 32194978 MeRIP-seq:(Medium) rs758997399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23436,Human_RBP_ID_3932380,Human_RBP_ID_5330929,Human_RBP_ID_5876754,Human_RBP_ID_8754554,Human_RBP_ID_17762269,Human_RBP_ID_18964344,Human_RBP_ID_19042457,Human_RBP_ID_22427903,Human_RBP_ID_22535762,Human_RBP_ID_22632572,Human_RBP_ID_22734461,Human_RBP_ID_22786417,Human_RBP_ID_24541752 Human_Splice_Rec_1058,Human_Splice_Rec_1098,Human_Splice_Rec_1136 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 66674 RMVar_ID_66674 Human_SNP_ID_144206 m1A Human chr1 - 957243 957243 957243 AGCCGGCGTAAAGGCCGTGCCTCTGAGCACAAAGACCAGCTCTCTCGGCTGAAGGACAGAGACCC AGCCGGCGTAAAGGCCGTGCCTCTGAGCACAAGGACCAGCTCTCTCGGCTGAAGGACAGAGACCC T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:957007..957330 32194978 MeRIP-seq:(Medium) rs756999177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223051,Human_RBP_ID_1755874,Human_RBP_ID_2170946,Human_RBP_ID_5876867,Human_RBP_ID_9357778,Human_RBP_ID_11138578,Human_RBP_ID_18582478 Human_Splice_Rec_1056,Human_Splice_Rec_1134 RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_128246,RMVar_hsa_circ_128249,RMVar_hsa_circ_85938 66675 RMVar_ID_66675 Human_SNP_ID_144345 m1A Human chr1 - 957539 957539 957539 AGCGCAGGGCACAGGCACAGCAAGTCCAGGGAAGACCGCGGCTGGGGGCCTGTGTAGCGCAGGGC AGCGCAGGGCACAGGCACAGCAAGTCCAGGGAGGACCGCGGCTGGGGGCCTGTGTAGCGCAGGGC T C NOC2L Ensembl:ENSG00000188976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:957536..957654 26863196 MeRIP-seq:(Medium) rs1401958144 Functional Loss SNV dbSNP153 33..33 33 - - - 66676 RMVar_ID_66676 Human_SNP_ID_144411 m1A Human chr1 + 957712 957712 957712 TCAAAACCGTTCGTGCCTCCTCTCAAACCACCACATAGTTCAATTCTCAGTTAACCTAAAGGTCT TCAAAACCGTTCGTGCCTCCTCTCAAACCACCGCATAGTTCAATTCTCAGTTAACCTAAAGGTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:957709..958028 26863196 MeRIP-seq:(Medium) rs761825421 Functional Loss SNV dbSNP153 33..33 33 - - - 66677 RMVar_ID_66677 Human_SNP_ID_144441 m1A Human chr1 - 957785 957785 957785 CCTCGTAAAACAGGGAGTTACTTCTGGGTTTGAGCGGTGGAGTGCCTTGTAGGTGACAAGGGTGG CCTCGTAAAACAGGGAGTTACTTCTGGGTTTGGGCGGTGGAGTGCCTTGTAGGTGACAAGGGTGG T C NOC2L Ensembl:ENSG00000188976 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:957780..958011 26863196 MeRIP-seq:(Medium) rs1296917127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25839,Human_RBP_ID_22488911,Human_RBP_ID_22557399,Human_RBP_ID_23418757 66678 RMVar_ID_66678 Human_SNP_ID_145035 m1A Human chr1 - 958988 958988 958988 TCCGAGTCCGAAAATTCTCCACAAGCGGAGACACGGGAAGCACGCGAGGCTGCCCGGAGTCCGGA TCCGAGTCCGAAAATTCTCCACAAGCGGAGACGCGGGAAGCACGCGAGGCTGCCCGGAGTCCGGA T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:958926..959050 26863196 MeRIP-seq:(Medium) rs1201876286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25842,Human_RBP_ID_1756067,Human_RBP_ID_8321155,Human_RBP_ID_8754556,Human_RBP_ID_22871675,Human_RBP_ID_23117588 Human_Splice_Rec_1054,Human_Splice_Rec_1055,Human_Splice_Rec_1132,Human_Splice_Rec_1133,Human_Splice_Rec_1144 66679 RMVar_ID_66679 Human_SNP_ID_145059 m1A Human chr1 + 959026 959026 959026 CGCTTGTGGAGAATTTTCGGACTCGGATTCGGACTCGGAGTCAAAGCCCGAAGCTAGGAACTCGT CGCTTGTGGAGAATTTTCGGACTCGGATTCGGGCTCGGAGTCAAAGCCCGAAGCTAGGAACTCGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:958826..959076 32194978 MeRIP-seq:(Medium) rs1444970492 Functional Loss SNV dbSNP153 33..33 33 - - - 66680 RMVar_ID_66680 Human_SNP_ID_145091 m1A Human chr1 - 959083 959077 959083 GTGCGGGCAGCTGTGACTCCTGCGTGACCCGCAGGCGCCTGGCGGAGCTGACGGTGGACGAGTTC GTGCGGGCAGCTGTGACTCCTGCGTGACCCGC______CTGGCGGAGCTGACGGTGGACGAGTTC GGCGCCT G NOC2L Ensembl:ENSG00000188976 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:958926..959100;chr1:958951..959100 26863196 MeRIP-seq:(Medium) rs1557625111 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4073376,Human_RBP_ID_5334360,Human_RBP_ID_18414807,Human_RBP_ID_22534633,Human_RBP_ID_22635265 66681 RMVar_ID_66681 Human_SNP_ID_145900 m1A Human chr1 + 960688 960688 960688 CGGGTCCTCCGCGAATCGGCGGTGGGTCCGGCAGCCGAATGCAGCCCCGCAGCGAGCGCCCGGCC CGGGTCCTCCGCGAATCGGCGGTGGGTCCGGCGGCCGAATGCAGCCCCGCAGCGAGCGCCCGGCC A G KLHL17 Ensembl:ENSG00000187961 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:960683..960810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3328957,Human_RBP_ID_18414808 66682 RMVar_ID_66682 Human_SNP_ID_145901 m1A Human chr1 + 960688 960688 960688 CGGGTCCTCCGCGAATCGGCGGTGGGTCCGGCAGCCGAATGCAGCCCCGCAGCGAGCGCCCGGCC CGGGTCCTCCGCGAATCGGCGGTGGGTCCGGCTGCCGAATGCAGCCCCGCAGCGAGCGCCCGGCC A T KLHL17 Ensembl:ENSG00000187961 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:960683..960810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3328957,Human_RBP_ID_18414808 66683 RMVar_ID_66683 Human_SNP_ID_145954 m1A Human chr1 + 960783 960783 960783 CCGGGGCCCGGGCCCGAGGCGCCGCCGCCTCCACCGCCGCAGCCGCCGGCGTGAGTGGGCGGGGG CCGGGGCCCGGGCCCGAGGCGCCGCCGCCTCCCCCGCCGCAGCCGCCGGCGTGAGTGGGCGGGGG A C KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:960686..960787 26863410 MeRIP-seq:(Medium) rs192245893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1145 66684 RMVar_ID_66684 Human_SNP_ID_146025 m1A Human chr1 - 960935 960935 960935 CGGGGCGCGGGTGGGGAACCTACTCCGGGCCGACCCCGCTCCGCACCTGAGTCCCGACCTCCCCC CGGGGCGCGGGTGGGGAACCTACTCCGGGCCGCCCCCGCTCCGCACCTGAGTCCCGACCTCCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:960599..961400 26863196 MeRIP-seq:(Medium) rs1042165363 Functional Loss SNV dbSNP153 33..33 33 - - - 66685 RMVar_ID_66685 Human_SNP_ID_146337 m1A Human chr1 - 961472 961472 961472 TGTGCGCACGGATCTCCTTGGCAGCCACGTGCAGGACGATGTCGCACAGGAGGCCGCGCTGGCGC TGTGCGCACGGATCTCCTTGGCAGCCACGTGCGGGACGATGTCGCACAGGAGGCCGCGCTGGCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:961353..961501 32194978 MeRIP-seq:(Medium) rs763623521 Functional Loss SNV dbSNP153 33..33 33 - - - 66686 RMVar_ID_66686 Human_SNP_ID_146385 m1A Human chr1 + 961552 961552 961552 CCTGCAGCCCCTACTTCCACGCCATGTTCACAAGCAAGTACCCGCCTGGGCGGCGCTGGGGGCTC CCTGCAGCCCCTACTTCCACGCCATGTTCACATGCAAGTACCCGCCTGGGCGGCGCTGGGGGCTC A T KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:961502..961640 26863196 MeRIP-seq:(Medium) rs766883571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19036163 66687 RMVar_ID_66687 Human_SNP_ID_146465 m1A Human chr1 + 961656 961656 961656 CGCAGATGAGATGAGCGAGAGCCGCCAGACCCACGTGACGCTGCACGACATCGACCCTCAGGCCT CGCAGATGAGATGAGCGAGAGCCGCCAGACCCGCGTGACGCTGCACGACATCGACCCTCAGGCCT A G KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:961606..961684 26863196 MeRIP-seq:(Medium) rs1338132720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22635900 Human_Splice_Rec_1147,Human_Splice_Rec_1179 RMVar_hsa_circ_128250,RMVar_hsa_circ_370291 66688 RMVar_ID_66688 Human_SNP_ID_147109 m1A Human chr1 + 962435 962435 962435 GAGGTCTACCGAGCCGTCCTGAGCTGGGTGAAACACGACGTGGACGCCCGCAGGCAGCATGTCCC GAGGTCTACCGAGCCGTCCTGAGCTGGGTGAAGCACGACGTGGACGCCCGCAGGCAGCATGTCCC A G KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:962384..962482 26863196 MeRIP-seq:(Medium) rs138271663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224697,Human_RBP_ID_18966616 Human_Splice_Rec_1150,Human_Splice_Rec_1151,Human_Splice_Rec_1165 66689 RMVar_ID_66689 Human_SNP_ID_147598 m1A Human chr1 + 963156 963156 963156 TTGCCATCCACGGAGACTGTGAGGCCTACGACACGCGCACCGACCGCTGGCACGTGGTGGCCTCC TTGCCATCCACGGAGACTGTGAGGCCTACGACTCGCGCACCGACCGCTGGCACGTGGTGGCCTCC A T KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:963109..963344 26863196 MeRIP-seq:(Medium) rs1335535849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22022536 Human_Splice_Rec_1154,Human_Splice_Rec_1155,Human_Splice_Rec_1168,Human_Splice_Rec_1169,Human_Splice_Rec_1183 66690 RMVar_ID_66690 Human_SNP_ID_147960 m1A Human chr1 - 963813 963813 963813 AGCGGAATGGCTGAAATCTTACCCTAGGAGTCAAACTCAGACCGCAAAGTCCTACCAGGCAGGGC AGCGGAATGGCTGAAATCTTACCCTAGGAGTCCAACTCAGACCGCAAAGTCCTACCAGGCAGGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:963793..963931 32194978 MeRIP-seq:(Medium) rs1557633425 Functional Loss SNV dbSNP153 33..33 33 - - - 66691 RMVar_ID_66691 Human_SNP_ID_148147 m1A Human chr1 + 964157 964157 964157 TGGGCGGCTACGACAGCTCCTCACACCTGGCCACTGTGGAGAAGTATGAGCCCCAGGTGCATAGT TGGGCGGCTACGACAGCTCCTCACACCTGGCCGCTGTGGAGAAGTATGAGCCCCAGGTGCATAGT A G KLHL17 Ensembl:ENSG00000187961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:964084..964202 26863196 MeRIP-seq:(Medium) rs192525640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849180,Human_RBP_ID_18966626,Human_RBP_ID_26313099,Human_RBP_ID_27555814 Human_Splice_Rec_1160,Human_Splice_Rec_1161,Human_Splice_Rec_1174,Human_Splice_Rec_1175,Human_Splice_Rec_1188,Human_Splice_Rec_1189,Human_Splice_Rec_1192 66692 RMVar_ID_66692 Human_SNP_ID_148317 m1A Human chr1 - 964420 964420 964420 GTGCCGTCGTTGCCCCCTGCCACGTACAGGGCACCCTCCAGCACGGCCACGCCCGCTGAGCTGCG GTGCCGTCGTTGCCCCCTGCCACGTACAGGGCGCCCTCCAGCACGGCCACGCCCGCTGAGCTGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:964369..964441 26863196 MeRIP-seq:(Medium) rs995611407 Functional Loss SNV dbSNP153 33..33 33 - - - 66693 RMVar_ID_66693 Human_SNP_ID_148931 m1A Human chr1 + 965223 965223 965223 ACCCACCTACCACCAGAGGCCTGCAGCCTCCCACATGCCTTAAGGGGACCGTGGCCCCCACCAGG ACCCACCTACCACCAGAGGCCTGCAGCCTCCCTCATGCCTTAAGGGGACCGTGGCCCCCACCAGG A T KLHL17 Ensembl:ENSG00000187961 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:965173..965275 26863196 MeRIP-seq:(Medium) rs371026821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364801 66694 RMVar_ID_66694 Human_SNP_ID_153406 m1A Human chr1 + 974928 974925 974929 AGGGCAGCACGGGCGTGAAGGTCGGAGGACAGAGAAAGGTCAGCAGGGTCAGAGTATGTGAGGTC AGGGCAGCACGGGCGTGAAGGTCGGAGGAC____AAAGGTCAGCAGGGTCAGAGTATGTGAGGTC CAGAG C PLEKHN1 Ensembl:ENSG00000187583 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:974823..975140 26863196 MeRIP-seq:(Medium) rs555848153 Functional Loss DEL dbSNP153 31..34 33 - - - 66695 RMVar_ID_66695 Human_SNP_ID_153407 m1A Human chr1 + 974928 974925 974929 AGGGCAGCACGGGCGTGAAGGTCGGAGGACAGAGAAAGGTCAGCAGGGTCAGAGTATGTGAGGTC AGGGCAGCACGGGCGTGAAGGTCGGAGGACAG__AAAGGTCAGCAGGGTCAGAGTATGTGAGGTC CAGAG CAG PLEKHN1 Ensembl:ENSG00000187583 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:974823..975140 26863196 MeRIP-seq:(Medium) rs555848153 Functional Loss DEL dbSNP153 33..34 33 - - - 66696 RMVar_ID_66696 Human_SNP_ID_154836 m1A Human chr1 + 978165 978165 978165 GGGAACCGCCTGCCTCCCCCTCCAACCCCAGGAACCGCCTGCCCCACCCTAACCCTGCACACTCT GGGAACCGCCTGCCTCCCCCTCCAACCCCAGGGACCGCCTGCCCCACCCTAACCCTGCACACTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:978133..978217 26863196 MeRIP-seq:(Medium) rs1253090305 Functional Loss SNV dbSNP153 33..33 33 - - - 66697 RMVar_ID_66697 Human_SNP_ID_158806 m1A Human chr1 + 988912 988912 988912 TTCAGGGTTGATTATTTCTGGTGTTCTGGGTTAATTGTTTCTGGAGTTCAGGGTTGATTGTTTCT TTCAGGGTTGATTATTTCTGGTGTTCTGGGTTGATTGTTTCTGGAGTTCAGGGTTGATTGTTTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:988894..989031 26863196 MeRIP-seq:(Medium) rs1181032059 Functional Loss SNV dbSNP153 33..33 33 - - - 66698 RMVar_ID_66698 Human_SNP_ID_162329 m1A Human chr1 + 999276 999276 999276 GGGACAGCGAGGCCGGGCGGCGGGAGGGTCCCAGCTGGCGCAGGCAGGCTGCCAGGTGGCCCAGC GGGACAGCGAGGCCGGGCGGCGGGAGGGTCCCCGCTGGCGCAGGCAGGCTGCCAGGTGGCCCAGC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:999174..999350 26863410 MeRIP-seq:(Medium) rs1249555272 Functional Loss SNV dbSNP153 33..33 33 - - - 66699 RMVar_ID_66699 Human_SNP_ID_162630 m1A Human chr1 + 999774 999774 999774 CGTTAATACGCGCTCGGCGCCGCTTCTCCATGACCGGCTTGGAGGACTGCGGGTCGGGCACCGGC CGTTAATACGCGCTCGGCGCCGCTTCTCCATGTCCGGCTTGGAGGACTGCGGGTCGGGCACCGGC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:999726..1000125 26863196 MeRIP-seq:(Medium) rs972828069 Functional Loss SNV dbSNP153 33..33 33 - - - 66700 RMVar_ID_66700 Human_SNP_ID_162804 m1A Human chr1 + 1000065 1000065 1000065 TGGCGGGCGAGCGGCGAGCGCGCGGCGATCCGAGCCCCTAGGGCGGATCCCGGCTCCAGGCCCGC TGGCGGGCGAGCGGCGAGCGCGCGGCGATCCGGGCCCCTAGGGCGGATCCCGGCTCCAGGCCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:999176..1000980 26863196 MeRIP-seq:(Medium) rs1186536367 Functional Loss SNV dbSNP153 33..33 33 - - - 66701 RMVar_ID_66701 Human_SNP_ID_162805 m1A Human chr1 + 1000065 1000065 1000065 TGGCGGGCGAGCGGCGAGCGCGCGGCGATCCGAGCCCCTAGGGCGGATCCCGGCTCCAGGCCCGC TGGCGGGCGAGCGGCGAGCGCGCGGCGATCCGTGCCCCTAGGGCGGATCCCGGCTCCAGGCCCGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:999176..1000980 26863196 MeRIP-seq:(Medium) rs1186536367 Functional Loss SNV dbSNP153 33..33 33 - - - 66702 RMVar_ID_66702 Human_SNP_ID_163105 m1A Human chr1 + 1000727 1000727 1000727 CAGAAAGCCTTGGGAGCGACAGAGCCGGGGGAAGGTCGGCGGCCGGGTCGGCAGGCGGGAGGGCG CAGAAAGCCTTGGGAGCGACAGAGCCGGGGGATGGTCGGCGGCCGGGTCGGCAGGCGGGAGGGCG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1000401..1000825 26863410 MeRIP-seq:(Medium) rs1557669104 Functional Loss SNV dbSNP153 33..33 33 - - - 66703 RMVar_ID_66703 Human_SNP_ID_163553 m1A Human chr1 + 1001994 1001989 1001994 TCCCCGGCCTGAGCGCTGGGCCCGGGCGGGAAAGCCCGCGAGCGCCCCCAGTGGCCGCAGTCGCC TCCCCGGCCTGAGCGCTGGGCCCGGGCG_____GCCCGCGAGCGCCCCCAGTGGCCGCAGTCGCC GGGAAA G ISG15 Ensembl:ENSG00000187608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1001963..1002061 26863196 MeRIP-seq:(Medium) rs1183049840 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_3330650,Human_RBP_ID_8051154,Human_RBP_ID_8165884 66704 RMVar_ID_66704 Human_SNP_ID_167046 m1A Human chr1 - 1013575 1013575 1013575 CACCTCCCCCCACCTGTGACATCTGCCTTACCATGGCTGTGGGCTGTGGGCTGTGGGCCACGGCA CACCTCCCCCCACCTGTGACATCTGCCTTACCGTGGCTGTGGGCTGTGGGCTGTGGGCCACGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1013539..1014244 32194978 MeRIP-seq:(Medium) rs1339641998 Functional Loss SNV dbSNP153 33..33 33 - - - 66705 RMVar_ID_66705 Human_SNP_ID_167226 m1A Human chr1 + 1014096 1014096 1014096 GAAGGCGCAGATCACCCAGAAGATCGGCGTGCACGCCTTCCAGCAGCGTCTGGCTGTCCACCCGA GAAGGCGCAGATCACCCAGAAGATCGGCGTGCGCGCCTTCCAGCAGCGTCTGGCTGTCCACCCGA A G ISG15 Ensembl:ENSG00000187608 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1014045..1014482 26863196 MeRIP-seq:(Medium) rs1422581357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27401984 RMVar_hsa_circ_108772,RMVar_hsa_circ_128252 66706 RMVar_ID_66706 Human_SNP_ID_170326 m1A Human chr1 - 1022253 1022253 1022253 CGCTGATCACCACCTTGTTGCCGCCGTCCAGCAGGCTCTCCCGGGCCACCAGGTCTTTGCCCTTC CGCTGATCACCACCTTGTTGCCGCCGTCCAGCGGGCTCTCCCGGGCCACCAGGTCTTTGCCCTTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1022201..1022300 32194978 MeRIP-seq:(Medium) rs545395744 Functional Loss SNV dbSNP153 33..33 33 - - - 66707 RMVar_ID_66707 Human_SNP_ID_170336 m1A Human chr1 + 1022267 1022267 1022267 TGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCC TGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCGACAAGGTGGTGATCAGCGGCTTTGGAGACCCC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:1022157..1022498;chr1:1022171..1022408;chr1:1022153..1022425;chr1:1022153..1022328 26863196 MeRIP-seq:(Medium) rs1199221617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305,Human_RBP_ID_98941,Human_RBP_ID_741218,Human_RBP_ID_4071528,Human_RBP_ID_26309941 Human_Splice_Rec_1332,Human_Splice_Rec_1402 Human_miRNA_ID_2170577 RMVar_hsa_circ_31777,RMVar_hsa_circ_88621,RMVar_hsa_circ_369580,RMVar_hsa_circ_128253,RMVar_hsa_circ_81095,RMVar_hsa_circ_128254,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255 66708 RMVar_ID_66708 Human_SNP_ID_170345 m1A Human chr1 + 1022282 1022282 1022282 GCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTGACAAC GCCTGCTGGACGGCGGCAACAAGGTGGTGATCGGCGGCTTTGGAGACCCCCTCATCTGTGACAAC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1022276..1022300 26863196 MeRIP-seq:(Medium) rs1202969499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305,Human_RBP_ID_98941,Human_RBP_ID_4072362 Human_Splice_Rec_1332,Human_Splice_Rec_1402 Human_miRNA_ID_2787522,Human_miRNA_ID_2817135 RMVar_hsa_circ_31777,RMVar_hsa_circ_88621,RMVar_hsa_circ_369580,RMVar_hsa_circ_128253,RMVar_hsa_circ_81095,RMVar_hsa_circ_128254,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255 66709 RMVar_ID_66709 Human_SNP_ID_172634 m1A Human chr1 + 1029440 1029409 1029440 TGGGGGGGACATCAGTGTCTATGCAGGCAGGTAGGGGGAGGGGGACATCCCGTGTCTATGAGGGC TG_______________________________GGGGGAGGGGGACATCCCGTGTCTATGAGGGC GGGGGGGACATCAGTGTCTATGCAGGCAGGTA G AGRN Ensembl:ENSG00000188157 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1029435..1029565 26863196 MeRIP-seq:(Medium) rs1278162664 Functional Loss DEL dbSNP153 3..33 33 - - - Human_RBP_ID_9411486 RMVar_hsa_circ_88621,RMVar_hsa_circ_369580,RMVar_hsa_circ_128253,RMVar_hsa_circ_81095,RMVar_hsa_circ_128254,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255 66710 RMVar_ID_66710 Human_SNP_ID_172660 m1A Human chr1 + 1029440 1029440 1029440 TGGGGGGGACATCAGTGTCTATGCAGGCAGGTAGGGGGAGGGGGACATCCCGTGTCTATGAGGGC TGGGGGGGACATCAGTGTCTATGCAGGCAGGTGGGGGGAGGGGGACATCCCGTGTCTATGAGGGC A G AGRN Ensembl:ENSG00000188157 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1029435..1029565 26863196 MeRIP-seq:(Medium) rs28387671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9411486 RMVar_hsa_circ_88621,RMVar_hsa_circ_369580,RMVar_hsa_circ_128253,RMVar_hsa_circ_81095,RMVar_hsa_circ_128254,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255 66711 RMVar_ID_66711 Human_SNP_ID_174804 m1A Human chr1 + 1035348 1035348 1035348 CTCCTGATGGTGAGTAGGGCTGAGTTCGGGGGACCTGGATGGGCTGTGGCACTCTTGGGAGTCAG CTCCTGATGGTGAGTAGGGCTGAGTTCGGGGGCCCTGGATGGGCTGTGGCACTCTTGGGAGTCAG A C AGRN Ensembl:ENSG00000188157 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1035342..1035449 26863196 MeRIP-seq:(Medium) rs1278451219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8724712,Human_RBP_ID_18157916,Human_RBP_ID_19036182,Human_RBP_ID_22350230,Human_RBP_ID_26773293 Human_Splice_Rec_1334,Human_Splice_Rec_1404,Human_Splice_Rec_1478,Human_Splice_Rec_1546 RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256 66712 RMVar_ID_66712 Human_SNP_ID_174808 m1A Human chr1 - 1035355 1035355 1035355 ATGGCCCCTGACTCCCAAGAGTGCCACAGCCCATCCAGGTCCCCCGAACTCAGCCCTACTCACCA ATGGCCCCTGACTCCCAAGAGTGCCACAGCCCGTCCAGGTCCCCCGAACTCAGCCCTACTCACCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1035351..1035444 26863196 MeRIP-seq:(Medium) rs1219741806 Functional Loss SNV dbSNP153 33..33 33 - - - 66713 RMVar_ID_66713 Human_SNP_ID_174905 m1A Human chr1 - 1035666 1035666 1035666 CCACCCCTTGCTGAACAGGGAGAAGGGAGGACAATAGAGCGGAGCCCCCTGACCGGACTCTGGCC CCACCCCTTGCTGAACAGGGAGAAGGGAGGACGATAGAGCGGAGCCCCCTGACCGGACTCTGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1035663..1036460 26863196 MeRIP-seq:(Medium) rs902403012 Functional Loss SNV dbSNP153 33..33 33 - - - 66714 RMVar_ID_66714 Human_SNP_ID_175018 m1A Human chr1 + 1035991 1035991 1035991 GTGAGGGGAAGAGAGGAAGTGGTCAGCTTTGCAGAGGAACACAGACGGGGGGACCGGTGGCTCCC GTGAGGGGAAGAGAGGAAGTGGTCAGCTTTGCGGAGGAACACAGACGGGGGGACCGGTGGCTCCC A G AGRN Ensembl:ENSG00000188157 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1035666..1036030 26863196 MeRIP-seq:(Medium) rs552734544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951,Human_RBP_ID_258306,Human_RBP_ID_801890,Human_RBP_ID_849183,Human_RBP_ID_1064213,Human_RBP_ID_3327735,Human_RBP_ID_5136552,Human_RBP_ID_5233663,Human_RBP_ID_5330937,Human_RBP_ID_8051189,Human_RBP_ID_8165932,Human_RBP_ID_8228487,Human_RBP_ID_9410327,Human_RBP_ID_18410024,Human_RBP_ID_18473042,Human_RBP_ID_18927632,Human_RBP_ID_21962674,Human_RBP_ID_22707805,Human_RBP_ID_23263117,Human_RBP_ID_26773699,Human_RBP_ID_27834970 RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256 66715 RMVar_ID_66715 Human_SNP_ID_176420 m1A Human chr1 + 1040654 1040654 1040654 CGGGCGTCTCGGCACCCTGAGCTTTCTCCCCTACCCGCCCCAGCGTGCCGGGGAATGCTGTGCGG CGGGCGTCTCGGCACCCTGAGCTTTCTCCCCTCCCCGCCCCAGCGTGCCGGGGAATGCTGTGCGG A C AGRN Ensembl:ENSG00000188157 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr1:1040651..1040900 26863196,32194978 MeRIP-seq:(Medium) rs1213490712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26,Human_RBP_ID_3329064,Human_RBP_ID_8165967,Human_RBP_ID_22534645,Human_RBP_ID_22635275 RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256 66716 RMVar_ID_66716 Human_SNP_ID_176487 m1A Human chr1 - 1040777 1040777 1040777 TTGCTGTAGGTGGAGGCGTCCGACCCACACACAGGCGCCACCACGCTGGGGCACGGGCTCTTCTT TTGCTGTAGGTGGAGGCGTCCGACCCACACACGGGCGCCACCACGCTGGGGCACGGGCTCTTCTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1040726..1040811 26863196 MeRIP-seq:(Medium) rs371764695 Functional Loss SNV dbSNP153 33..33 33 - - - 66717 RMVar_ID_66717 Human_SNP_ID_176493 m1A Human chr1 + 1040791 1040791 1040791 CCCCAGCGTGGTGGCGCCTGTGTGTGGGTCGGACGCCTCCACCTACAGCAACGAATGCGAGCTGC CCCCAGCGTGGTGGCGCCTGTGTGTGGGTCGGGCGCCTCCACCTACAGCAACGAATGCGAGCTGC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1040616..1040882 26863196 MeRIP-seq:(Medium) rs1306784685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853368,Human_RBP_ID_8754562 Human_Splice_Rec_1337,Human_Splice_Rec_1407,Human_Splice_Rec_1481,Human_Splice_Rec_1549,Human_Splice_Rec_1621 RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256 66718 RMVar_ID_66718 Human_SNP_ID_176807 m1A Human chr1 + 1041376 1041376 1041376 GCCGCGCCTGCGCCCGCCAGGAGAATGTCTTCAAGAAGTTCGACGGCCCTTGTGGTGAGCGCGGC GCCGCGCCTGCGCCCGCCAGGAGAATGTCTTCGAGAAGTTCGACGGCCCTTGTGGTGAGCGCGGC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1041151..1041400 26863196 MeRIP-seq:(Medium) rs1351237560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_290335,Human_RBP_ID_23423531 Human_Splice_Rec_1339,Human_Splice_Rec_1409,Human_Splice_Rec_1483,Human_Splice_Rec_1551 RMVar_hsa_circ_67997,RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256 66719 RMVar_ID_66719 Human_SNP_ID_176940 m1A Human chr1 + 1041583 1041583 1041583 GCTCCTACGGCCCGAGAGCTGCCCTGCCCGGCAGGCGCCAGTGTGTGGGGACGACGGAGTCACCT GCTCCTACGGCCCGAGAGCTGCCCTGCCCGGCGGGCGCCAGTGTGTGGGGACGACGGAGTCACCT A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1041453..1041725 26863196 MeRIP-seq:(Medium) rs150359724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9269510,Human_RBP_ID_18966643,Human_RBP_ID_22427911,Human_RBP_ID_22751634,Human_RBP_ID_23423532 RMVar_hsa_circ_67997,RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_83903,RMVar_hsa_circ_128257 66720 RMVar_ID_66720 Human_SNP_ID_177786 m1A Human chr1 + 1043376 1043376 1043376 TCTACGATCCTGTGTGCGGCAGCGACGGCGTCACATACGGCAGCGCGTGCGAGCTGGAGGCCACG TCTACGATCCTGTGTGCGGCAGCGACGGCGTCGCATACGGCAGCGCGTGCGAGCTGGAGGCCACG A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1043226..1043750 26863196 MeRIP-seq:(Medium) rs1294309821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313,Human_RBP_ID_18964361,Human_RBP_ID_22750552 Human_Splice_Rec_1345,Human_Splice_Rec_1415,Human_Splice_Rec_1489,Human_Splice_Rec_1557 RMVar_hsa_circ_18675,RMVar_hsa_circ_67997,RMVar_hsa_circ_81095,RMVar_hsa_circ_16274,RMVar_hsa_circ_128255,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_83903,RMVar_hsa_circ_128257,RMVar_hsa_circ_121371,RMVar_hsa_circ_128261,RMVar_hsa_circ_92828,RMVar_hsa_circ_102299,RMVar_hsa_circ_128263,RMVar_hsa_circ_89920,RMVar_hsa_circ_128262,RMVar_hsa_circ_128259,RMVar_hsa_circ_128260,RMVar_hsa_circ_128258 66721 RMVar_ID_66721 Human_SNP_ID_178108 m1A Human chr1 - 1043920 1043920 1043920 CAGGCACTGCCGTAGGTGACACCGTCGCTGCCACACACGGGGCCGGGCGGGGGGTGCTCACACCG CAGGCACTGCCGTAGGTGACACCGTCGCTGCCGCACACGGGGCCGGGCGGGGGGTGCTCACACCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1043876..1044150 26863196 MeRIP-seq:(Medium) rs1409094645 Functional Loss SNV dbSNP153 33..33 33 - - - 66722 RMVar_ID_66722 Human_SNP_ID_178379 m1A Human chr1 + 1044425 1044425 1044425 TGAGTCACAGCGAGGGCTCTACGTAGCGGCCCAGGGAGCCTGCCGAGGTGAGCCGGCTGCACGTG TGAGTCACAGCGAGGGCTCTACGTAGCGGCCCGGGGAGCCTGCCGAGGTGAGCCGGCTGCACGTG A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:1044326..1044425 26863196,32194978 MeRIP-seq:(Medium) rs765044467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934774,Human_RBP_ID_18431064,Human_RBP_ID_18966659 Human_Splice_Rec_1352,Human_Splice_Rec_1353,Human_Splice_Rec_1422,Human_Splice_Rec_1423,Human_Splice_Rec_1496,Human_Splice_Rec_1497,Human_Splice_Rec_1564,Human_Splice_Rec_1565 RMVar_hsa_circ_18675,RMVar_hsa_circ_16274,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_121371,RMVar_hsa_circ_128261,RMVar_hsa_circ_92828,RMVar_hsa_circ_102299,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_128259,RMVar_hsa_circ_128260,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_125212,RMVar_hsa_circ_128266 66723 RMVar_ID_66723 Human_SNP_ID_178790 m1A Human chr1 - 1045381 1045381 1045381 GTGGCTGGGTCACAGGTGCCGCCGTAAGAGCCATGGGGGTTGCACTGGCAGGCACCTGAAAGGCC GTGGCTGGGTCACAGGTGCCGCCGTAAGAGCCGTGGGGGTTGCACTGGCAGGCACCTGAAAGGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1045376..1045400 26863196 MeRIP-seq:(Medium) rs776644156 Functional Loss SNV dbSNP153 33..33 33 - - - 66724 RMVar_ID_66724 Human_SNP_ID_178819 m1A Human chr1 + 1045435 1045435 1045435 GACCCAGCCACAGGCCAGTGCTCCTGCCGCCCAGGTGTGGGGGGCCTCAGGTGTGACCGCTGTGA GACCCAGCCACAGGCCAGTGCTCCTGCCGCCCTGGTGTGGGGGGCCTCAGGTGTGACCGCTGTGA A T AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1045426..1045450 26863196 MeRIP-seq:(Medium) rs1260235453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744279,Human_RBP_ID_8754573,Human_RBP_ID_18468377 Human_Splice_Rec_1356,Human_Splice_Rec_1357,Human_Splice_Rec_1426,Human_Splice_Rec_1427,Human_Splice_Rec_1500,Human_Splice_Rec_1501,Human_Splice_Rec_1568,Human_Splice_Rec_1569,Human_Splice_Rec_1623 RMVar_hsa_circ_18675,RMVar_hsa_circ_16274,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128261,RMVar_hsa_circ_102299,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_58736,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_82920,RMVar_hsa_circ_125212,RMVar_hsa_circ_128266,RMVar_hsa_circ_115507,RMVar_hsa_circ_128267,RMVar_hsa_circ_128268 66725 RMVar_ID_66725 Human_SNP_ID_178844 m1A Human chr1 + 1045481 1045481 1045481 TCAGGTGTGACCGCTGTGAGCCTGGCTTCTGGAACTTTCGAGGCATCGTCACCGATGGCCGGAGT TCAGGTGTGACCGCTGTGAGCCTGGCTTCTGGGACTTTCGAGGCATCGTCACCGATGGCCGGAGT A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1045140..1045553 26863196 MeRIP-seq:(Medium) rs574793544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23321,Human_RBP_ID_744279,Human_RBP_ID_1758009,Human_RBP_ID_18468377 Human_Splice_Rec_1357,Human_Splice_Rec_1427,Human_Splice_Rec_1501,Human_Splice_Rec_1569,Human_Splice_Rec_1623 RMVar_hsa_circ_18675,RMVar_hsa_circ_16274,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128261,RMVar_hsa_circ_102299,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_58736,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_82920,RMVar_hsa_circ_125212,RMVar_hsa_circ_128266,RMVar_hsa_circ_115507,RMVar_hsa_circ_128267,RMVar_hsa_circ_128268 66726 RMVar_ID_66726 Human_SNP_ID_178845 m1A Human chr1 + 1045482 1045482 1045482 CAGGTGTGACCGCTGTGAGCCTGGCTTCTGGAACTTTCGAGGCATCGTCACCGATGGCCGGAGTG CAGGTGTGACCGCTGTGAGCCTGGCTTCTGGAGCTTTCGAGGCATCGTCACCGATGGCCGGAGTG A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1045351..1045522 26863196 MeRIP-seq:(Medium) rs761152280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23321,Human_RBP_ID_744279,Human_RBP_ID_18468377 Human_Splice_Rec_1357,Human_Splice_Rec_1427,Human_Splice_Rec_1501,Human_Splice_Rec_1569,Human_Splice_Rec_1623 RMVar_hsa_circ_18675,RMVar_hsa_circ_16274,RMVar_hsa_circ_120384,RMVar_hsa_circ_128256,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128261,RMVar_hsa_circ_102299,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_58736,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_82920,RMVar_hsa_circ_125212,RMVar_hsa_circ_128266,RMVar_hsa_circ_115507,RMVar_hsa_circ_128267,RMVar_hsa_circ_128268 66727 RMVar_ID_66727 Human_SNP_ID_178999 m1A Human chr1 - 1045815 1045815 1045815 CGGCCGTCTGGACACTGCCCACACTTGGGTCCAGCCACCCCGGGCTTACACGAGCACAGCCCCGT CGGCCGTCTGGACACTGCCCACACTTGGGTCCGGCCACCCCGGGCTTACACGAGCACAGCCCCGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1045732..1046275 26863196 MeRIP-seq:(Medium) rs779599910 Functional Loss SNV dbSNP153 33..33 33 - - - 66728 RMVar_ID_66728 Human_SNP_ID_179141 m1A Human chr1 - 1046035 1046035 1046035 ACAGGTGAGCATCGGGCAGACACAGTGGGCTGAGCCAGACTCCTCCACGCACCGCGCACCGAACT ACAGGTGAGCATCGGGCAGACACAGTGGGCTGTGCCAGACTCCTCCACGCACCGCGCACCGAACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1045898..1046200 26863196 MeRIP-seq:(Medium) rs765693278 Functional Loss SNV dbSNP153 33..33 33 - - - 66729 RMVar_ID_66729 Human_SNP_ID_179336 m1A Human chr1 - 1046407 1046407 1046407 GTCACGGAGGCAGATGTCGGGTGAGTGCTGGGAGCAACAGCCTCTGCAAGGAGAGGGAGGTTGGC GTCACGGAGGCAGATGTCGGGTGAGTGCTGGGGGCAACAGCCTCTGCAAGGAGAGGGAGGTTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1046396..1046600 26863196 MeRIP-seq:(Medium) rs374308932 Functional Loss SNV dbSNP153 33..33 33 - - - 66730 RMVar_ID_66730 Human_SNP_ID_179343 m1A Human chr1 + 1046423 1046423 1046423 TTGCAGAGGCTGTTGCTCCCAGCACTCACCCGACATCTGCCTCCGTGACTGTGACCACCCCAGGG TTGCAGAGGCTGTTGCTCCCAGCACTCACCCGTCATCTGCCTCCGTGACTGTGACCACCCCAGGG A T AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1045962..1046704 26863196 MeRIP-seq:(Medium) rs1441488678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23326,Human_RBP_ID_22632595,Human_RBP_ID_24556396 Human_Splice_Rec_1364,Human_Splice_Rec_1434,Human_Splice_Rec_1508,Human_Splice_Rec_1576 Human_miRNA_ID_158887,Human_miRNA_ID_705439,Human_miRNA_ID_712687,Human_miRNA_ID_2473806,Human_miRNA_ID_2959592 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_86198,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_96584,RMVar_hsa_circ_128271,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_128270,RMVar_hsa_circ_87140,RMVar_hsa_circ_336283,RMVar_hsa_circ_128275 66731 RMVar_ID_66731 Human_SNP_ID_179446 m1A Human chr1 - 1046589 1046589 1046589 GTGCCGTGGGGGGCACCGTCAGCACGGGCCACACGGTGGTCCTGGGGACGCTGGCAGTGGTCCGA GTGCCGTGGGGGGCACCGTCAGCACGGGCCACGCGGTGGTCCTGGGGACGCTGGCAGTGGTCCGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1046551..1046600 26863196 MeRIP-seq:(Medium) rs1292494843 Functional Loss SNV dbSNP153 33..33 33 - - - 66732 RMVar_ID_66732 Human_SNP_ID_179989 m1A Human chr1 + 1047663 1047663 1047663 GGGACCTGGGGCCCGGCAAATCCGTCCGCGCCATTGTGGATGTGCACTTTGACCCCAGTGAGACC GGGACCTGGGGCCCGGCAAATCCGTCCGCGCCGTTGTGGATGTGCACTTTGACCCCAGTGAGACC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1047614..1047691 26863196 MeRIP-seq:(Medium) rs778562449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932407,Human_RBP_ID_9357788,Human_RBP_ID_18966675,Human_RBP_ID_23423651 Human_Splice_Rec_1370,Human_Splice_Rec_1371,Human_Splice_Rec_1440,Human_Splice_Rec_1441,Human_Splice_Rec_1514,Human_Splice_Rec_1515,Human_Splice_Rec_1582,Human_Splice_Rec_1583,Human_Splice_Rec_1630,Human_Splice_Rec_1631,Human_Splice_Rec_1633 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_96584,RMVar_hsa_circ_128271,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_128275 66733 RMVar_ID_66733 Human_SNP_ID_179990 m1A Human chr1 + 1047663 1047663 1047663 GGGACCTGGGGCCCGGCAAATCCGTCCGCGCCATTGTGGATGTGCACTTTGACCCCAGTGAGACC GGGACCTGGGGCCCGGCAAATCCGTCCGCGCCTTTGTGGATGTGCACTTTGACCCCAGTGAGACC A T AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1047614..1047691 26863196 MeRIP-seq:(Medium) rs778562449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932407,Human_RBP_ID_9357788,Human_RBP_ID_18966675,Human_RBP_ID_23423651 Human_Splice_Rec_1370,Human_Splice_Rec_1371,Human_Splice_Rec_1440,Human_Splice_Rec_1441,Human_Splice_Rec_1514,Human_Splice_Rec_1515,Human_Splice_Rec_1582,Human_Splice_Rec_1583,Human_Splice_Rec_1630,Human_Splice_Rec_1631,Human_Splice_Rec_1633 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_96584,RMVar_hsa_circ_128271,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_128275 66734 RMVar_ID_66734 Human_SNP_ID_180103 m1A Human chr1 - 1047848 1047848 1047848 GCACGTGCTCCTGCAGCGGCCGCCTCACCCCCAAGGACCGGCGCCTGGACACCTGGATCTGCCGG GCACGTGCTCCTGCAGCGGCCGCCTCACCCCCGAGGACCGGCGCCTGGACACCTGGATCTGCCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1047801..1047875 32194978 MeRIP-seq:(Medium) rs1339449252 Functional Loss SNV dbSNP153 33..33 33 - - - 66735 RMVar_ID_66735 Human_SNP_ID_180231 m1A Human chr1 + 1048076 1048076 1048076 TCAGGAGCCATTGCTGCGGGAGCCACGGCCAGAGCCACCACTGCATCGCGCCTGCCGTCCTCTGC TCAGGAGCCATTGCTGCGGGAGCCACGGCCAGCGCCACCACTGCATCGCGCCTGCCGTCCTCTGC A C AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1048026..1048100 26863196 MeRIP-seq:(Medium) rs1442317576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9269530,Human_RBP_ID_9318359,Human_RBP_ID_22022540,Human_RBP_ID_22750566,Human_RBP_ID_27402126 Human_Splice_Rec_1374,Human_Splice_Rec_1444,Human_Splice_Rec_1518,Human_Splice_Rec_1586 Human_miRNA_ID_3067627 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_96584,RMVar_hsa_circ_128271,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_76558,RMVar_hsa_circ_106719,RMVar_hsa_circ_128275,RMVar_hsa_circ_128276,RMVar_hsa_circ_128277 66736 RMVar_ID_66736 Human_SNP_ID_180284 m1A Human chr1 + 1048164 1048164 1048164 CCAGTCACACAAGCCAGCCCGTTGCCAAGACCACGGCAGCCCCCACCACACGTCGGCCCCCCACC CCAGTCACACAAGCCAGCCCGTTGCCAAGACCGCGGCAGCCCCCACCACACGTCGGCCCCCCACC A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1048001..1048272 26863196 MeRIP-seq:(Medium) rs1392350160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23338 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_96584,RMVar_hsa_circ_128271,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_76558,RMVar_hsa_circ_106719,RMVar_hsa_circ_128275,RMVar_hsa_circ_128276,RMVar_hsa_circ_128277 66737 RMVar_ID_66737 Human_SNP_ID_180299 m1A Human chr1 - 1048184 1048184 1048184 GGCACACGGCTGGGGGCAGTGGTGGGGGGCCGACGTGTGGTGGGGGCTGCCGTGGTCTTGGCAAC GGCACACGGCTGGGGGCAGTGGTGGGGGGCCGCCGTGTGGTGGGGGCTGCCGTGGTCTTGGCAAC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1048026..1048250 26863196 MeRIP-seq:(Medium) rs746943998 Functional Loss SNV dbSNP153 33..33 33 - - - 66738 RMVar_ID_66738 Human_SNP_ID_180694 m1A Human chr1 + 1048920 1048920 1048920 CCTTCGAGGGCCGCTCCTTCCTGGCCTTCCCCACTCTCCGCGCCTACCACACGCTGCGCCTGGCA CCTTCGAGGGCCGCTCCTTCCTGGCCTTCCCCCCTCTCCGCGCCTACCACACGCTGCGCCTGGCA A C AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1048858..1048995;chr1:1048836..1048992 26863196 MeRIP-seq:(Medium) rs777090547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23342,Human_RBP_ID_5336424,Human_RBP_ID_22427930,Human_RBP_ID_22750570 Human_Splice_Rec_1376,Human_Splice_Rec_1446,Human_Splice_Rec_1520,Human_Splice_Rec_1588 Human_miRNA_ID_2724522 RMVar_hsa_circ_18675,RMVar_hsa_circ_114133,RMVar_hsa_circ_123730,RMVar_hsa_circ_128263,RMVar_hsa_circ_128262,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_102374,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_128272,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_76558,RMVar_hsa_circ_106719,RMVar_hsa_circ_128275,RMVar_hsa_circ_128276,RMVar_hsa_circ_128277 66739 RMVar_ID_66739 Human_SNP_ID_181728 m1A Human chr1 + 1050470 1050470 1050470 CGCTGGAGGTCGTGTTCCTGGCACGAGGCCCCAGCGGCCTCCTGCTCTACAACGGGCAGAAGACG CGCTGGAGGTCGTGTTCCTGGCACGAGGCCCCCGCGGCCTCCTGCTCTACAACGGGCAGAAGACG A C AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1050419..1050525 26863196 MeRIP-seq:(Medium) rs1204321867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853391,Human_RBP_ID_3932415,Human_RBP_ID_18966687,Human_RBP_ID_22427938,Human_RBP_ID_22750582 Human_Splice_Rec_1386,Human_Splice_Rec_1456,Human_Splice_Rec_1530,Human_Splice_Rec_1598 RMVar_hsa_circ_18675,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_110757,RMVar_hsa_circ_128275,RMVar_hsa_circ_128279 66740 RMVar_ID_66740 Human_SNP_ID_181765 m1A Human chr1 + 1050540 1050540 1050540 CAAGGGGGACTTCGTGTCGCTGGCACTGCGGGACCGCCGCCTGGAGTTCCGCTACGACCTGGGCA CAAGGGGGACTTCGTGTCGCTGGCACTGCGGGCCCGCCGCCTGGAGTTCCGCTACGACCTGGGCA A C AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1050418..1050542 26863196 MeRIP-seq:(Medium) rs1157133853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932416,Human_RBP_ID_9269534,Human_RBP_ID_9318360,Human_RBP_ID_18966688,Human_RBP_ID_22427939,Human_RBP_ID_22750583 Human_Splice_Rec_1387,Human_Splice_Rec_1457,Human_Splice_Rec_1531,Human_Splice_Rec_1599 RMVar_hsa_circ_18675,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_110757,RMVar_hsa_circ_128275,RMVar_hsa_circ_128279 66741 RMVar_ID_66741 Human_SNP_ID_182982 m1A Human chr1 - 1052842 1052780 1052843 CCACATATACACACACATACATGGACCCATGGACACACACTCGGACACACACCTGCGTGTCTCCC CCACATATACACACACATACATGGACCCATG__________________________________ ACATGGGTCCATGTATGTGTGTGTATATGAGGGAGACACGCAGGTGTGTGTCCGAGTGTGTGTC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1052837..1053034 26863196 MeRIP-seq:(Medium) rs1557724415 Functional Loss DEL dbSNP153 32..65 33 - - - 66742 RMVar_ID_66742 Human_SNP_ID_183361 m1A Human chr1 - 1053656 1053656 1053656 GGAGGACAAGGGCCCCAGCTGCGGAGGCCACAAGGGCTGTGACGGGACCCAGGGGTGGCTGGTGG GGAGGACAAGGGCCCCAGCTGCGGAGGCCACAGGGGCTGTGACGGGACCCAGGGGTGGCTGGTGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1053651..1053825 26863196 MeRIP-seq:(Medium) rs376491084 Functional Loss SNV dbSNP153 33..33 33 - - - 66743 RMVar_ID_66743 Human_SNP_ID_184003 m1A Human chr1 + 1055076 1055076 1055076 TGATATGATTTTCTTGCCTGAGTGTTGGCCGGAGGGACTGCTGGCCCGGCCTCCCTTCCGTCCAG TGATATGATTTTCTTGCCTGAGTGTTGGCCGGGGGGACTGCTGGCCCGGCCTCCCTTCCGTCCAG A G AL645608.5,AGRN Ensembl:ENSG00000242590,Ensembl:ENSG00000188157 lincRNA,Protein coding exon,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1055026..1055200 32194978 MeRIP-seq:(Medium) rs1176247058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223361,Human_RBP_ID_744833,Human_RBP_ID_801403,Human_RBP_ID_856511,Human_RBP_ID_1438462,Human_RBP_ID_3932423,Human_RBP_ID_4077300,Human_RBP_ID_5086328,Human_RBP_ID_5108354,Human_RBP_ID_5135992,Human_RBP_ID_5161443,Human_RBP_ID_5541626,Human_RBP_ID_5640846,Human_RBP_ID_8171973,Human_RBP_ID_8243868,Human_RBP_ID_8753382,Human_RBP_ID_9252573,Human_RBP_ID_11174863,Human_RBP_ID_21879578,Human_RBP_ID_23205627,Human_RBP_ID_23423851,Human_RBP_ID_24400163,Human_RBP_ID_24455018,Human_RBP_ID_27402139 Human_miRNA_ID_3162188,Human_miRNA_ID_3188687,Human_miRNA_ID_3189752,Human_miRNA_ID_3190258,Human_miRNA_ID_3190477 66744 RMVar_ID_66744 Human_SNP_ID_184048 m1A Human chr1 + 1055187 1055187 1055187 GGTGGCAGCGTGGAGGGCTCGGCGTGGATGGCAGCCTCAGGACACACACCCCTGCCTCAAGGTGC GGTGGCAGCGTGGAGGGCTCGGCGTGGATGGCGGCCTCAGGACACACACCCCTGCCTCAAGGTGC A G AL645608.5,AGRN Ensembl:ENSG00000242590,Ensembl:ENSG00000188157 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1055015..1055403 26863196 MeRIP-seq:(Medium) rs973231691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5091983,Human_RBP_ID_5254152,Human_RBP_ID_5541626,Human_RBP_ID_17764555,Human_RBP_ID_24455020,Human_RBP_ID_27402140 Human_Splice_Rec_1641 Human_miRNA_ID_1393605,Human_miRNA_ID_3191711,Human_miRNA_ID_3211902 66745 RMVar_ID_66745 Human_SNP_ID_187169 m1A Human chr1 + 1064506 1064506 1064506 CCCCACGGCCGGATGAGAAGTGGGAGACGGGGAGCGTTTTGACACCCTCGGAGACCCGGTGTAGC CCCCACGGCCGGATGAGAAGTGGGAGACGGGGGGCGTTTTGACACCCTCGGAGACCCGGTGTAGC A G AL390719.1 Ensembl:ENSG00000217801 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1064454..1064676 26863196 MeRIP-seq:(Medium) rs961911009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3327772,Human_RBP_ID_5538532,Human_RBP_ID_8052047 Human_Splice_Rec_1659,Human_Splice_Rec_1663,Human_Splice_Rec_1665 66746 RMVar_ID_66746 Human_SNP_ID_188385 m1A Human chr1 - 1068476 1068476 1068476 GGGAGTGCCCAAGCGGAGGGGCTGCGGGAGCCAAGGCGAGCAGGAGGAGGAGGAAGGAAATGGGG GGGAGTGCCCAAGCGGAGGGGCTGCGGGAGCCGAGGCGAGCAGGAGGAGGAGGAAGGAAATGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1068469..1068561 26863196 MeRIP-seq:(Medium) rs1472710615 Functional Loss SNV dbSNP153 33..33 33 - - - 66747 RMVar_ID_66747 Human_SNP_ID_188487 m1A Human chr1 + 1068789 1068789 1068789 CTGTGCAGATGCAGGTGCGGCGGGGCGGGGCCACGCGGGCTGTGCAGGTGCAGGTGCGGCGGGGC CTGTGCAGATGCAGGTGCGGCGGGGCGGGGCCCCGCGGGCTGTGCAGGTGCAGGTGCGGCGGGGC A C AL390719.1 Ensembl:ENSG00000217801 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1068779..1069016 26863196 MeRIP-seq:(Medium) rs1389194644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241285 66748 RMVar_ID_66748 Human_SNP_ID_188590 m1A Human chr1 - 1068934 1068934 1068934 CAGGATGTCAATCACGATGATGGTGCCCGTGCATCCGATGCCCCCACTGAGGACAAACTAGGCGG CAGGATGTCAATCACGATGATGGTGCCCGTGCGTCCGATGCCCCCACTGAGGACAAACTAGGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1068932..1069021 26863196 MeRIP-seq:(Medium) rs1335638979 Functional Loss SNV dbSNP153 33..33 33 - - - 66749 RMVar_ID_66749 Human_SNP_ID_188705 m1A Human chr1 + 1069174 1069174 1069174 GCCCCGCCCCTGCCTGCCGGCACCTTCCCCCCATCCGTAGCCCCTCCCCAAGCGCGCTTGTCCGC GCCCCGCCCCTGCCTGCCGGCACCTTCCCCCCCTCCGTAGCCCCTCCCCAAGCGCGCTTGTCCGC A C AL390719.1 Ensembl:ENSG00000217801 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1069137..1069317 26863196 MeRIP-seq:(Medium) rs1404959067 Functional Loss SNV dbSNP153 33..33 33 - - - 66750 RMVar_ID_66750 Human_SNP_ID_193498 m1A Human chr1 + 1083912 1083912 1083912 GTGTCTGTGGCCCCGCACATAAAATGGGTCCTAACCGGGCTGACTCTTGGGTCCGCCTGACCCAG GTGTCTGTGGCCCCGCACATAAAATGGGTCCTCACCGGGCTGACTCTTGGGTCCGCCTGACCCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1083909..1084073 26863196 MeRIP-seq:(Medium) rs773721720 Functional Loss SNV dbSNP153 33..33 33 - - - 66751 RMVar_ID_66751 Human_SNP_ID_194934 m1A Human chr1 + 1087831 1087831 1087831 CTGCGCACCCTGACCCTGAGTACTCCGACCCCAAGTACTCCACGCTGCACTCTCCACGCCGAGCA CTGCGCACCCTGACCCTGAGTACTCCGACCCCGAGTACTCCACGCTGCACTCTCCACGCCGAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1087796..1088089 26863196 MeRIP-seq:(Medium) rs903673124 Functional Loss SNV dbSNP153 33..33 33 - - - 66752 RMVar_ID_66752 Human_SNP_ID_194941 m1A Human chr1 - 1087844 1087844 1087844 CTCGGGGCCGGGGTGCTCGGCGTGGAGAGTGCAGCGTGGAGTACTTGGGGTCGGAGTACTCAGGG CTCGGGGCCGGGGTGCTCGGCGTGGAGAGTGCGGCGTGGAGTACTTGGGGTCGGAGTACTCAGGG T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1087840..1087929 26863196 MeRIP-seq:(Medium) rs564662509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3329106,Human_RBP_ID_18474485 66753 RMVar_ID_66753 Human_SNP_ID_195194 m1A Human chr1 - 1088397 1088397 1088397 GTGGGCCTATCCTGCTTGGGCGGCATGAGGGAACACGGGGTGCGAGGCAGCCGCTCCAGGCACTG GTGGGCCTATCCTGCTTGGGCGGCATGAGGGAGCACGGGGTGCGAGGCAGCCGCTCCAGGCACTG T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1088361..1088581 26863196 MeRIP-seq:(Medium) rs1251755905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8165995,Human_RBP_ID_9410801 66754 RMVar_ID_66754 Human_SNP_ID_195533 m1A Human chr1 - 1089442 1089440 1089442 GAGGAGGAGGGCACCGCTCTGAGGGAGAACAGAGGGGCTGGGAGGAAGCTGAGCACCTTGGGGTC GAGGAGGAGGGCACCGCTCTGAGGGAGAACAG__GGGCTGGGAGGAAGCTGAGCACCTTGGGGTC CCT C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1089438..1089636 26863196 MeRIP-seq:(Medium) rs1452827213 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_258637,Human_RBP_ID_3327781,Human_RBP_ID_3932431,Human_RBP_ID_5234164,Human_RBP_ID_8051225,Human_RBP_ID_8940070,Human_RBP_ID_18473071,Human_RBP_ID_19040635,Human_RBP_ID_21961657,Human_RBP_ID_22632610 66755 RMVar_ID_66755 Human_SNP_ID_201291 m1A Human chr1 - 1108471 1108471 1108471 ATGGTGGCTGTGGTGGACGGTGCTGCTGAGACATGGTGGCTGTGGTGAACGGTGTCGAGACATGG ATGGTGGCTGTGGTGGACGGTGCTGCTGAGACGTGGTGGCTGTGGTGAACGGTGTCGAGACATGG T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1108470..1108610 26863196 MeRIP-seq:(Medium) rs1221429854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5641307,Human_RBP_ID_23319626 66756 RMVar_ID_66756 Human_SNP_ID_202566 m1A Human chr1 + 1112480 1112480 1112480 CGCATGCTCCCTCCTTCCAGTGAACACACGGCACATGCTACCTCCCTCCAGTGAACACACGGCAC CGCATGCTCCCTCCTTCCAGTGAACACACGGCGCATGCTACCTCCCTCCAGTGAACACACGGCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1112456..1112625 26863196 MeRIP-seq:(Medium) rs1424068404 Functional Loss SNV dbSNP153 33..33 33 - - - 66757 RMVar_ID_66757 Human_SNP_ID_203611 m1A Human chr1 - 1115830 1115830 1115830 CGCCGCCTCCCAACGAGCCTGGCCGCGGTCCTATGGGGGAAAGGCGCCCGGGCTGAGCGGGACGC CGCCGCCTCCCAACGAGCCTGGCCGCGGTCCTGTGGGGGAAAGGCGCCCGGGCTGAGCGGGACGC T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1115828..1115965 26863196 MeRIP-seq:(Medium) rs1395605894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5336444 66758 RMVar_ID_66758 Human_SNP_ID_237261 m1A Human chr1 - 1217052 1217051 1217052 AACTTCGCTGGAAATGAGTAGCCAGGAAGTTCAGGGGAGGGTGCCGGGTCCTTCCCGGGCCTGGC AACTTCGCTGGAAATGAGTAGCCAGGAAGTTC_GGGGAGGGTGCCGGGTCCTTCCCGGGCCTGGC CT C SDF4 Ensembl:ENSG00000078808 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1217001..1217131 26863196 MeRIP-seq:(Medium) rs199634793 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17712,Human_RBP_ID_322193,Human_RBP_ID_4079012,Human_RBP_ID_5108359,Human_RBP_ID_5234460,Human_RBP_ID_17646216,Human_RBP_ID_22427949,Human_RBP_ID_26385011,Human_RBP_ID_27165454 Human_miRNA_ID_118481,Human_miRNA_ID_122292,Human_miRNA_ID_958564,Human_miRNA_ID_2451310,Human_miRNA_ID_3114810 RMVar_hsa_circ_101468,RMVar_hsa_circ_128285 66759 RMVar_ID_66759 Human_SNP_ID_237453 m1A Human chr1 - 1217475 1217475 1217475 CCGGCCGCGCCCCGCGCCGCCCCCCACGCACCACCGGGGCGGCCTCGCGGGTGACTCCGGGCTCC CCGGCCGCGCCCCGCGCCGCCCCCCACGCACCGCCGGGGCGGCCTCGCGGGTGACTCCGGGCTCC T C SDF4 Ensembl:ENSG00000078808 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:1217426..1217700 32194978 MeRIP-seq:(Medium) rs1396125164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322474,Human_RBP_ID_4079149,Human_RBP_ID_18187450,Human_RBP_ID_22022546,Human_RBP_ID_27386266 RMVar_hsa_circ_101468,RMVar_hsa_circ_128285 66760 RMVar_ID_66760 Human_SNP_ID_237563 m1A Human chr1 - 1217660 1217660 1217660 GCAGAGCTACATGGACCCCATGAACGAGTACAACGCGCTGAACGAGGCCAAGCAGATGATCGCCG GCAGAGCTACATGGACCCCATGAACGAGTACAGCGCGCTGAACGAGGCCAAGCAGATGATCGCCG T C SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:1217526..1217700 26863196 MeRIP-seq:(Medium) rs374737222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1409151,Human_RBP_ID_1723142,Human_RBP_ID_8282035,Human_RBP_ID_10539031 Human_Splice_Rec_2102,Human_Splice_Rec_2142,Human_Splice_Rec_2144 Human_miRNA_ID_1037690,Human_miRNA_ID_2477078 RMVar_hsa_circ_101468,RMVar_hsa_circ_128285 66761 RMVar_ID_66761 Human_SNP_ID_237859 m1A Human chr1 + 1218456 1218456 1218456 GCCGGCTCCGGGACACGGCTGCGCCAGGGCTCACCTCCAGCTCCTCGGCGGTCACGATGCCGTCG GCCGGCTCCGGGACACGGCTGCGCCAGGGCTCGCCTCCAGCTCCTCGGCGGTCACGATGCCGTCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1218451..1218500 26863196 MeRIP-seq:(Medium) rs1239043313 Functional Loss SNV dbSNP153 33..33 33 - - - 66762 RMVar_ID_66762 Human_SNP_ID_237889 m1A Human chr1 - 1218526 1218523 1218527 GCCAGGACATTGACGACAACTGGGTGAAAGACAGAAAAAAGGAGTTTGAGGAGCTCATTGACTCC GCCAGGACATTGACGACAACTGGGTGAAAGA____AAAAAGGAGTTTGAGGAGCTCATTGACTCC TTCTG T SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1218426..1218671 26863196 MeRIP-seq:(Medium) rs1280256385 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_17715,Human_RBP_ID_271702,Human_RBP_ID_1409166,Human_RBP_ID_1723160,Human_RBP_ID_8282053,Human_RBP_ID_17674656,Human_RBP_ID_18548435,Human_RBP_ID_23325497 Human_Splice_Rec_2101,Human_Splice_Rec_2113,Human_Splice_Rec_2125,Human_Splice_Rec_2137,Human_Splice_Rec_2141,Human_Splice_Rec_2143 Human_miRNA_ID_1098549,Human_miRNA_ID_2516030 RMVar_hsa_circ_101468,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286 66763 RMVar_ID_66763 Human_SNP_ID_237900 m1A Human chr1 - 1218546 1218546 1218546 CACCGTGGAGAACCAGCAGGGCCAGGACATTGACGACAACTGGGTGAAAGACAGAAAAAAGGAGT CACCGTGGAGAACCAGCAGGGCCAGGACATTGGCGACAACTGGGTGAAAGACAGAAAAAAGGAGT T C SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1218441..1218660 26863196 MeRIP-seq:(Medium) rs1464583243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17715,Human_RBP_ID_271702,Human_RBP_ID_322655,Human_RBP_ID_1409167,Human_RBP_ID_1723160,Human_RBP_ID_3277900,Human_RBP_ID_10539246,Human_RBP_ID_22750601,Human_RBP_ID_27152680 Human_Splice_Rec_2100,Human_Splice_Rec_2101,Human_Splice_Rec_2112,Human_Splice_Rec_2113,Human_Splice_Rec_2124,Human_Splice_Rec_2125,Human_Splice_Rec_2136,Human_Splice_Rec_2137,Human_Splice_Rec_2140,Human_Splice_Rec_2141,Human_Splice_Rec_2143,Human_Splice_Rec_2152 RMVar_hsa_circ_101468,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286 66764 RMVar_ID_66764 Human_SNP_ID_238025 m1A Human chr1 - 1218828 1218828 1218828 GCTGACGGAGGAGGAGTTCCTGTCGTTCCTCCACCCCGAGCACAGCCGGGGAATGCTCAGGTTCA GCTGACGGAGGAGGAGTTCCTGTCGTTCCTCCTCCCCGAGCACAGCCGGGGAATGCTCAGGTTCA T A SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1218826..1218875 26863196 MeRIP-seq:(Medium) rs1191821136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17716,Human_RBP_ID_322656,Human_RBP_ID_3984608,Human_RBP_ID_5137296,Human_RBP_ID_9355283,Human_RBP_ID_22427957,Human_RBP_ID_22750604 Human_Splice_Rec_2098,Human_Splice_Rec_2099,Human_Splice_Rec_2110,Human_Splice_Rec_2111,Human_Splice_Rec_2123,Human_Splice_Rec_2134,Human_Splice_Rec_2135,Human_Splice_Rec_2139,Human_Splice_Rec_2151 Human_miRNA_ID_3076124 RMVar_hsa_circ_101468,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_128287 66765 RMVar_ID_66765 Human_SNP_ID_238092 m1A Human chr1 + 1218962 1218962 1218962 GAGAGGGGCGCAGCCTGTGGGTATCGAGGCCGACAGACGCCAGCACGCAAATCCAGAAAGTTCCG GAGAGGGGCGCAGCCTGTGGGTATCGAGGCCGGCAGACGCCAGCACGCAAATCCAGAAAGTTCCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1218948..1219048 26863410 MeRIP-seq:(Medium) rs757215619 Functional Loss SNV dbSNP153 33..33 33 - - - 66766 RMVar_ID_66766 Human_SNP_ID_238384 m1A Human chr1 - 1219648 1219648 1219648 TCGGGGTGAGGGCCCGTTGGGGCCGGGTGGGCACGGCAGGAGAGCGGGGGCCACACACCCAGAGG TCGGGGTGAGGGCCCGTTGGGGCCGGGTGGGCCCGGCAGGAGAGCGGGGGCCACACACCCAGAGG T G SDF4 Ensembl:ENSG00000078808 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1219646..1219766 26863196 MeRIP-seq:(Medium) rs1252462007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258645,Human_RBP_ID_3327804,Human_RBP_ID_5158240,Human_RBP_ID_5233683,Human_RBP_ID_5311377,Human_RBP_ID_5641319,Human_RBP_ID_8051242,Human_RBP_ID_8166031,Human_RBP_ID_8227912,Human_RBP_ID_8724540,Human_RBP_ID_9318372,Human_RBP_ID_9410818,Human_RBP_ID_17101437,Human_RBP_ID_17204298,Human_RBP_ID_17338752,Human_RBP_ID_17646088,Human_RBP_ID_18157329,Human_RBP_ID_18414811,Human_RBP_ID_18455300,Human_RBP_ID_18473097,Human_RBP_ID_21961661,Human_RBP_ID_22470265,Human_RBP_ID_22707272,Human_RBP_ID_22779240,Human_RBP_ID_23263329,Human_RBP_ID_26773725 RMVar_hsa_circ_101468,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_128287 66767 RMVar_ID_66767 Human_SNP_ID_239814 m1A Human chr1 - 1223297 1223295 1223298 GAAGTTTTTGGCGAGTAAAGGCCATAGCGAGAAGGAGGTTGCCGACGCCATCAGGCTCAACGAGG GAAGTTTTTGGCGAGTAAAGGCCATAGCGAG___GAGGTTGCCGACGCCATCAGGCTCAACGAGG CCTT C SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:1223197..1224006;chr1:1223226..1223375 26863196 MeRIP-seq:(Medium) rs756891917 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_741657,Human_RBP_ID_1064216,Human_RBP_ID_1409172,Human_RBP_ID_3984638,Human_RBP_ID_17445190,Human_RBP_ID_17722427,Human_RBP_ID_18548446,Human_RBP_ID_22748798,Human_RBP_ID_22779245,Human_RBP_ID_26313104,Human_RBP_ID_26838475 Human_Splice_Rec_2096,Human_Splice_Rec_2097,Human_Splice_Rec_2108,Human_Splice_Rec_2109,Human_Splice_Rec_2120,Human_Splice_Rec_2121,Human_Splice_Rec_2132,Human_Splice_Rec_2133,Human_Splice_Rec_2148,Human_Splice_Rec_2149 RMVar_hsa_circ_101468,RMVar_hsa_circ_128288,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_274426,RMVar_hsa_circ_128287,RMVar_hsa_circ_305956,RMVar_hsa_circ_128289 66768 RMVar_ID_66768 Human_SNP_ID_239826 m1A Human chr1 - 1223316 1223316 1223316 CTTGGGACGAGTATAAGGTGAAGTTTTTGGCGAGTAAAGGCCATAGCGAGAAGGAGGTTGCCGAC CTTGGGACGAGTATAAGGTGAAGTTTTTGGCGCGTAAAGGCCATAGCGAGAAGGAGGTTGCCGAC T G SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1223268..1231981 32194978 MeRIP-seq:(Medium) rs1232791669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17718,Human_RBP_ID_1064216,Human_RBP_ID_1409173,Human_RBP_ID_2088306,Human_RBP_ID_22748798,Human_RBP_ID_23325596,Human_RBP_ID_26313104 Human_Splice_Rec_2096,Human_Splice_Rec_2097,Human_Splice_Rec_2108,Human_Splice_Rec_2109,Human_Splice_Rec_2120,Human_Splice_Rec_2121,Human_Splice_Rec_2132,Human_Splice_Rec_2133,Human_Splice_Rec_2148,Human_Splice_Rec_2149 RMVar_hsa_circ_101468,RMVar_hsa_circ_128288,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_274426,RMVar_hsa_circ_128287,RMVar_hsa_circ_305956,RMVar_hsa_circ_128289 66769 RMVar_ID_66769 Human_SNP_ID_240029 m1A Human chr1 - 1223829 1223826 1223830 ACTTCCGCGCCGTGGACCCTGACGGGGACGGTACTGTGGCTGGGCCGGGGTGGGTGGGGCGGTGG ACTTCCGCGCCGTGGACCCTGACGGGGACGG____GTGGCTGGGCCGGGGTGGGTGGGGCGGTGG CAGTA C SDF4 Ensembl:ENSG00000078808 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1223826..1223850 26863196 MeRIP-seq:(Medium) rs1250857064 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_101468,RMVar_hsa_circ_128288,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_274426,RMVar_hsa_circ_128287,RMVar_hsa_circ_305956,RMVar_hsa_circ_128289 66770 RMVar_ID_66770 Human_SNP_ID_240031 m1A Human chr1 - 1223829 1223829 1223829 ACTTCCGCGCCGTGGACCCTGACGGGGACGGTACTGTGGCTGGGCCGGGGTGGGTGGGGCGGTGG ACTTCCGCGCCGTGGACCCTGACGGGGACGGTGCTGTGGCTGGGCCGGGGTGGGTGGGGCGGTGG T C SDF4 Ensembl:ENSG00000078808 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1223826..1223850 26863196 MeRIP-seq:(Medium) rs536494768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101468,RMVar_hsa_circ_128288,RMVar_hsa_circ_77688,RMVar_hsa_circ_374095,RMVar_hsa_circ_128285,RMVar_hsa_circ_128286,RMVar_hsa_circ_274426,RMVar_hsa_circ_128287,RMVar_hsa_circ_305956,RMVar_hsa_circ_128289 66771 RMVar_ID_66771 Human_SNP_ID_241851 m1A Human chr1 + 1228877 1228877 1228877 CAGAGGAGGAAGTGAGGTCCTGGCTCCAATCCAATCCCCGGGCACCACGGAGGGCTCTGTGTCCC CAGAGGAGGAAGTGAGGTCCTGGCTCCAATCCGATCCCCGGGCACCACGGAGGGCTCTGTGTCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1228826..1228981 26863196 MeRIP-seq:(Medium) rs1356090811 Functional Loss SNV dbSNP153 33..33 33 - - - 66772 RMVar_ID_66772 Human_SNP_ID_242846 m1A Human chr1 + 1231933 1231933 1231933 TCCCCGCGCTCGGGATCCGAGGACCGGAGCGAAGCGTCAGTGACGCCGCCAACGGGCCCGGATCA TCCCCGCGCTCGGGATCCGAGGACCGGAGCGATGCGTCAGTGACGCCGCCAACGGGCCCGGATCA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1231931..1232031 26863410 MeRIP-seq:(Medium) rs952125713 Functional Loss SNV dbSNP153 33..33 33 - - - 66773 RMVar_ID_66773 Human_SNP_ID_243049 m1A Human chr1 - 1232355 1232355 1232355 CGGGCTCGGCCGCGCAGCGCGCCAGGTAGAGCAGCGCCGCCCCGCACAGCGCCAGCGTGCCCAGG CGGGCTCGGCCGCGCAGCGCGCCAGGTAGAGCGGCGCCGCCCCGCACAGCGCCAGCGTGCCCAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1232306..1232489 26863196 MeRIP-seq:(Medium) rs1553151166 Functional Loss SNV dbSNP153 33..33 33 - - - 66774 RMVar_ID_66774 Human_SNP_ID_243349 m1A Human chr1 + 1232889 1232889 1232889 GCCGGGGGGGCGCTGGCGCGAGGCCGCCTGGCAACTCTGCGACTACTACCTGCCCTACGCGCTGG GCCGGGGGGGCGCTGGCGCGAGGCCGCCTGGCCACTCTGCGACTACTACCTGCCCTACGCGCTGG A C B3GALT6 Ensembl:ENSG00000176022 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1232537..1232956 26863196 MeRIP-seq:(Medium) rs769997051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27165656,Human_RBP_ID_27402221 66775 RMVar_ID_66775 Human_SNP_ID_244036 m1A Human chr1 - 1234546 1234546 1234546 TGTGCACACACGGGCGGTCAGTCCTGGATTCAAGGTGGCCCATCGGAGCTCGAACTCAACGGCCT TGTGCACACACGGGCGGTCAGTCCTGGATTCAGGGTGGCCCATCGGAGCTCGAACTCAACGGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1234495..1234793 32194978 MeRIP-seq:(Medium) rs866119278 Functional Loss SNV dbSNP153 33..33 33 - - - 66776 RMVar_ID_66776 Human_SNP_ID_246825 m1A Human chr1 - 1242539 1242538 1242539 TCCGGGCTGCTCCTGGGCACGTGAGGGCGCCCAGGGGGGCTGGCGAGGAGCTGCCGCCGGATCCC TCCGGGCTGCTCCTGGGCACGTGAGGGCGCCC_GGGGGGCTGGCGAGGAGCTGCCGCCGGATCCC CT C C1QTNF12 Ensembl:ENSG00000184163 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1242532..1242769 26863196 MeRIP-seq:(Medium) rs3835300 Functional Loss DEL dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_323080 66777 RMVar_ID_66777 Human_SNP_ID_246826 m1A Human chr1 - 1242539 1242539 1242539 TCCGGGCTGCTCCTGGGCACGTGAGGGCGCCCAGGGGGGCTGGCGAGGAGCTGCCGCCGGATCCC TCCGGGCTGCTCCTGGGCACGTGAGGGCGCCCGGGGGGGCTGGCGAGGAGCTGCCGCCGGATCCC T C C1QTNF12 Ensembl:ENSG00000184163 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1242532..1242769 26863196 MeRIP-seq:(Medium) rs770415126 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_323080 66778 RMVar_ID_66778 Human_SNP_ID_247821 m1A Human chr1 - 1244499 1244499 1244499 GCCTCAGTGCGCTAGCCCCGTCCCGTCCCTTCAGCCATCCCAGGCCTCAGGACCTGAGTTCTCCG GCCTCAGTGCGCTAGCCCCGTCCCGTCCCTTCGGCCATCCCAGGCCTCAGGACCTGAGTTCTCCG T C C1QTNF12 Ensembl:ENSG00000184163 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1244353..1244704 26863196 MeRIP-seq:(Medium) rs773801104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1409399,Human_RBP_ID_3327825,Human_RBP_ID_9410826,Human_RBP_ID_22635950 66779 RMVar_ID_66779 Human_SNP_ID_249001 m1A Human chr1 + 1247156 1247156 1247156 CAAAGGTCCACCTCATTCTGGGAACCGTGAAGACAGCAGCCTACCTCCTCGCCCTCCCTGCCAGC CAAAGGTCCACCTCATTCTGGGAACCGTGAAGGCAGCAGCCTACCTCCTCGCCCTCCCTGCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1247150..1247217 26863196 MeRIP-seq:(Medium) rs969329531 Functional Loss SNV dbSNP153 33..33 33 - - - 66780 RMVar_ID_66780 Human_SNP_ID_249040 m1A Human chr1 - 1247305 1247305 1247305 CCCTGGGCCGGGGCCGTGAGTCAGGGCGGGGCACCCGGGGGAGCCTGGGTGAGGAGGTCGTGGGA CCCTGGGCCGGGGCCGTGAGTCAGGGCGGGGCCCCCGGGGGAGCCTGGGTGAGGAGGTCGTGGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1247296..1247371 26863196 MeRIP-seq:(Medium) rs1417309634 Functional Loss SNV dbSNP153 33..33 33 - - - 66781 RMVar_ID_66781 Human_SNP_ID_252630 m1A Human chr1 + 1257925 1257925 1257925 CCTGGATTCGGGCCTCATTCATGGCTCTTCACACGTCCTCCCCTCCCAAGCTCTCAAATCCACCT CCTGGATTCGGGCCTCATTCATGGCTCTTCACGCGTCCTCCCCTCCCAAGCTCTCAAATCCACCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1257433..1258029 26863196 MeRIP-seq:(Medium) rs1438821048 Functional Loss SNV dbSNP153 33..33 33 - - - 66782 RMVar_ID_66782 Human_SNP_ID_255946 m1A Human chr1 - 1267986 1267986 1267986 GTCAGTGTAGACGTTGCTTTTAACAGATGAGCAGCACCAGCAGTAAGAGGGCTCCGACCACGGCA GTCAGTGTAGACGTTGCTTTTAACAGATGAGCTGCACCAGCAGTAAGAGGGCTCCGACCACGGCA T A UBE2J2 Ensembl:ENSG00000160087 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1267919..1268043;chr1:1267876..1268182 26863196 MeRIP-seq:(Medium) rs376707325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189940,Human_RBP_ID_4073392,Human_RBP_ID_17668289,Human_RBP_ID_22485650,Human_RBP_ID_22557455,Human_RBP_ID_24578859 Human_Splice_Rec_2184,Human_Splice_Rec_2198,Human_Splice_Rec_2210,Human_Splice_Rec_2232,Human_Splice_Rec_2246,Human_Splice_Rec_2258,Human_Splice_Rec_2274,Human_Splice_Rec_2286,Human_Splice_Rec_2312,Human_Splice_Rec_2322,Human_Splice_Rec_2332,Human_Splice_Rec_2346,Human_Splice_Rec_2356,Human_Splice_Rec_2362,Human_Splice_Rec_2366 Human_miRNA_ID_2050122,Human_miRNA_ID_2050123 RMVar_hsa_circ_271597,RMVar_hsa_circ_128293,RMVar_hsa_circ_294271,RMVar_hsa_circ_105699,RMVar_hsa_circ_128298,RMVar_hsa_circ_128299,RMVar_hsa_circ_324070,RMVar_hsa_circ_277770,RMVar_hsa_circ_128302,RMVar_hsa_circ_128301,RMVar_hsa_circ_315031 66783 RMVar_ID_66783 Human_SNP_ID_255947 m1A Human chr1 - 1267986 1267986 1267986 GTCAGTGTAGACGTTGCTTTTAACAGATGAGCAGCACCAGCAGTAAGAGGGCTCCGACCACGGCA GTCAGTGTAGACGTTGCTTTTAACAGATGAGCGGCACCAGCAGTAAGAGGGCTCCGACCACGGCA T C UBE2J2 Ensembl:ENSG00000160087 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1267919..1268043;chr1:1267876..1268182 26863196 MeRIP-seq:(Medium) rs376707325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189940,Human_RBP_ID_4073392,Human_RBP_ID_17668289,Human_RBP_ID_22485650,Human_RBP_ID_22557455,Human_RBP_ID_24578859 Human_Splice_Rec_2184,Human_Splice_Rec_2198,Human_Splice_Rec_2210,Human_Splice_Rec_2232,Human_Splice_Rec_2246,Human_Splice_Rec_2258,Human_Splice_Rec_2274,Human_Splice_Rec_2286,Human_Splice_Rec_2312,Human_Splice_Rec_2322,Human_Splice_Rec_2332,Human_Splice_Rec_2346,Human_Splice_Rec_2356,Human_Splice_Rec_2362,Human_Splice_Rec_2366 Human_miRNA_ID_2050122,Human_miRNA_ID_2050123 RMVar_hsa_circ_271597,RMVar_hsa_circ_128293,RMVar_hsa_circ_294271,RMVar_hsa_circ_105699,RMVar_hsa_circ_128298,RMVar_hsa_circ_128299,RMVar_hsa_circ_324070,RMVar_hsa_circ_277770,RMVar_hsa_circ_128302,RMVar_hsa_circ_128301,RMVar_hsa_circ_315031 66784 RMVar_ID_66784 Human_SNP_ID_256661 m1A Human chr1 + 1270477 1270477 1270477 AGCTCAGCCAGGGCACCCAACGCGTGCTCCCAAATGTGTGGCCTCAGCACCACCCCCAACCCTGC AGCTCAGCCAGGGCACCCAACGCGTGCTCCCACATGTGTGGCCTCAGCACCACCCCCAACCCTGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1270475..1271026 26863196 MeRIP-seq:(Medium) rs986649822 Functional Loss SNV dbSNP153 33..33 33 - - - 66785 RMVar_ID_66785 Human_SNP_ID_256770 m1A Human chr1 + 1270817 1270817 1270817 TTGCCTGCCAGCCCCTTGACAGAGGCAGCCCCAGCCAGCCCTCCTCATTCCCAGCTCCCAAGACA TTGCCTGCCAGCCCCTTGACAGAGGCAGCCCCGGCCAGCCCTCCTCATTCCCAGCTCCCAAGACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1270816..1270926 26863196 MeRIP-seq:(Medium) rs373802458 Functional Loss SNV dbSNP153 33..33 33 - - - 66786 RMVar_ID_66786 Human_SNP_ID_257332 m1A Human chr1 - 1272638 1272638 1272638 CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGATGAGTGACAGGCAGGTGACCCAGGCAGGTGCA CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGTTGAGTGACAGGCAGGTGACCCAGGCAGGTGCA T A UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1272636..1272748 26863196 MeRIP-seq:(Medium) rs1356782589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741080,Human_RBP_ID_1064383,Human_RBP_ID_3327871,Human_RBP_ID_8051309,Human_RBP_ID_10552390,Human_RBP_ID_18415204,Human_RBP_ID_23263245 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 66787 RMVar_ID_66787 Human_SNP_ID_257333 m1A Human chr1 - 1272638 1272638 1272638 CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGATGAGTGACAGGCAGGTGACCCAGGCAGGTGCA CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGGTGAGTGACAGGCAGGTGACCCAGGCAGGTGCA T C UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1272636..1272748 26863196 MeRIP-seq:(Medium) rs1356782589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741080,Human_RBP_ID_1064383,Human_RBP_ID_3327871,Human_RBP_ID_8051309,Human_RBP_ID_10552390,Human_RBP_ID_18415204,Human_RBP_ID_23263245 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 66788 RMVar_ID_66788 Human_SNP_ID_257761 m1A Human chr1 - 1273781 1273781 1273781 GGCGGCGGCGCTGCGGCGGGTTCGGTGGGCCCAATCCCGGGGCGGTGCGGCTGTTTCGGGCGCGG GGCGGCGGCGCTGCGGCGGGTTCGGTGGGCCCGATCCCGGGGCGGTGCGGCTGTTTCGGGCGCGG T C UBE2J2 Ensembl:ENSG00000160087 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1273651..1273850 26863196 MeRIP-seq:(Medium) rs1340566404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323774,Human_RBP_ID_4072389,Human_RBP_ID_9318388,Human_RBP_ID_10552567,Human_RBP_ID_17723596,Human_RBP_ID_27554275,Human_RBP_ID_27834998 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 66789 RMVar_ID_66789 Human_SNP_ID_257762 m1A Human chr1 - 1273781 1273781 1273781 GGCGGCGGCGCTGCGGCGGGTTCGGTGGGCCCAATCCCGGGGCGGTGCGGCTGTTTCGGGCGCGG GGCGGCGGCGCTGCGGCGGGTTCGGTGGGCCCCATCCCGGGGCGGTGCGGCTGTTTCGGGCGCGG T G UBE2J2 Ensembl:ENSG00000160087 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1273651..1273850 26863196 MeRIP-seq:(Medium) rs1340566404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323774,Human_RBP_ID_4072389,Human_RBP_ID_9318388,Human_RBP_ID_10552567,Human_RBP_ID_17723596,Human_RBP_ID_27554275,Human_RBP_ID_27834998 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 66790 RMVar_ID_66790 Human_SNP_ID_257780 m1A Human chr1 - 1273820 1273800 1273820 TTCCGCCCCGCGAGCGGCCATCTTGGAGGCTGAGGCGGCGGCGGCGGCGCTGCGGCGGGTTCGGT TTCCGCCCCGCGAGCGGCCATCTTGGAGGCTG____________________CGGCGGGTTCGGT GCAGCGCCGCCGCCGCCGCCT G UBE2J2 Ensembl:ENSG00000160087 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1273725..1273835 26863410 MeRIP-seq:(Medium) rs1473769518 Functional Loss DEL dbSNP153 33..52 33 - - - Human_RBP_ID_323774,Human_RBP_ID_4073393,Human_RBP_ID_27834998 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 66791 RMVar_ID_66791 Human_SNP_ID_257945 m1A Human chr1 - 1274078 1274078 1274078 GGGCCTGCCGCCCTGGGCCGTGGCACATGGGGAGGGAAGCGCGCGGCTTCGGGGTCTGGGGCTCT GGGCCTGCCGCCCTGGGCCGTGGCACATGGGGGGGGAAGCGCGCGGCTTCGGGGTCTGGGGCTCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1274077..1274240 26863196 MeRIP-seq:(Medium) rs1237555751 Functional Loss SNV dbSNP153 33..33 33 - - - 66792 RMVar_ID_66792 Human_SNP_ID_257954 m1A Human chr1 - 1274114 1274114 1274114 GTCGGGGTTCTTTCTCCACCGGGGTCGCCCTCAGCCGGGCCTGCCGCCCTGGGCCGTGGCACATG GTCGGGGTTCTTTCTCCACCGGGGTCGCCCTCCGCCGGGCCTGCCGCCCTGGGCCGTGGCACATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1274064..1274202 26863196 MeRIP-seq:(Medium) rs981350077 Functional Loss SNV dbSNP153 33..33 33 - - - 66793 RMVar_ID_66793 Human_SNP_ID_259442 m1A Human chr1 + 1279156 1279156 1279156 TGTGGCCTGGGGTTCCGTGGAGCAGGTTGAGTATGGAGGAACTGGGGTTCCGTGGAGCAGGTGGG TGTGGCCTGGGGTTCCGTGGAGCAGGTTGAGTGTGGAGGAACTGGGGTTCCGTGGAGCAGGTGGG A G LINC01786 Ensembl:ENSG00000230415 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1275222..1279266 26863196 MeRIP-seq:(Medium) rs1169585300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2368,Human_Splice_Rec_2372 RMVar_hsa_circ_128303 66794 RMVar_ID_66794 Human_SNP_ID_261053 m1A Human chr1 - 1283938 1283938 1283938 AAACAGGCTGGCTGGGCGTGGGACTGTGCTGCAGGCGAGGGAGGACCCAGCCAGGGCAGCCACAC AAACAGGCTGGCTGGGCGTGGGACTGTGCTGCGGGCGAGGGAGGACCCAGCCAGGGCAGCCACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1283935..1284060 26863196 MeRIP-seq:(Medium) rs1008784196 Functional Loss SNV dbSNP153 33..33 33 - - - 66795 RMVar_ID_66795 Human_SNP_ID_261490 m1A Human chr1 - 1284370 1284370 1284370 GGGCCAGGCATCGGAAAGAGACCCCCCAACCCAGCCCCTGGTACCTCAAGGTGGGAGCCCCCCCG GGGCCAGGCATCGGAAAGAGACCCCCCAACCCCGCCCCTGGTACCTCAAGGTGGGAGCCCCCCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1284363..1284678 26863196 MeRIP-seq:(Medium) rs1404303391 Functional Loss SNV dbSNP153 33..33 33 - - - 66796 RMVar_ID_66796 Human_SNP_ID_262565 m1A Human chr1 + 1286836 1286836 1286836 CGAGTTTGCCAGGGAGAACATTGACTCCCTGTACAACGTCAACCTCAGCAAAGGCAGAGCCGCCC CGAGTTTGCCAGGGAGAACATTGACTCCCTGTTCAACGTCAACCTCAGCAAAGGCAGAGCCGCCC A T SCNN1D Ensembl:ENSG00000162572 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1286829..1286931 26863196 MeRIP-seq:(Medium) rs1331039777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2384,Human_Splice_Rec_2414,Human_Splice_Rec_2440,Human_Splice_Rec_2468,Human_Splice_Rec_2500 66797 RMVar_ID_66797 Human_SNP_ID_266800 m1A Human chr1 - 1293555 1293555 1293555 AGCCTCCACCTGGAAGAGAGCTAGGGCCGGGCAGGCCGGGCAGCTGCCACCCCGCCCGGCCCGAC AGCCTCCACCTGGAAGAGAGCTAGGGCCGGGCGGGCCGGGCAGCTGCCACCCCGCCCGGCCCGAC T C ACAP3 Ensembl:ENSG00000131584 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1293551..1293575 26863196 MeRIP-seq:(Medium) rs1215581044 Functional Loss SNV dbSNP153 33..33 33 - - - 66798 RMVar_ID_66798 Human_SNP_ID_267482 m1A Human chr1 - 1294605 1294605 1294605 TCCCCACAGAGGGTGCAGAGTCGGAGGAGTCCAGCGGTGAGGCAGACGGGGACACTGAGGCCGAG TCCCCACAGAGGGTGCAGAGTCGGAGGAGTCCGGCGGTGAGGCAGACGGGGACACTGAGGCCGAG T C ACAP3 Ensembl:ENSG00000131584 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1294126..1294825 26863196 MeRIP-seq:(Medium) rs1384307764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518289,Human_RBP_ID_8753414,Human_RBP_ID_18964390 Human_Splice_Rec_2572,Human_Splice_Rec_2618,Human_Splice_Rec_2644,Human_Splice_Rec_2684,Human_Splice_Rec_2692 RMVar_hsa_circ_14878,RMVar_hsa_circ_128304,RMVar_hsa_circ_97034 66799 RMVar_ID_66799 Human_SNP_ID_267491 m1A Human chr1 + 1294617 1294617 1294617 GTCCCCGTCTGCCTCACCGCTGGACTCCTCCGACTCTGCACCCTCTGTGGGGAGGGGGCGGTCAG GTCCCCGTCTGCCTCACCGCTGGACTCCTCCGGCTCTGCACCCTCTGTGGGGAGGGGGCGGTCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1294088..1294825 26863196 MeRIP-seq:(Medium) rs1310682363 Functional Loss SNV dbSNP153 33..33 33 - - - 66800 RMVar_ID_66800 Human_SNP_ID_268096 m1A Human chr1 + 1295922 1295922 1295922 AAACTTCTTTTCCACGTATTTGTCCTTGATCCAGGCCTCCTTGTCCTGCCTGGACCAGGGGGGAA AAACTTCTTTTCCACGTATTTGTCCTTGATCCGGGCCTCCTTGTCCTGCCTGGACCAGGGGGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1295726..1296102 26863196 MeRIP-seq:(Medium) rs1214185685 Functional Loss SNV dbSNP153 33..33 33 - - - 66801 RMVar_ID_66801 Human_SNP_ID_269767 m1A Human chr1 + 1299288 1299288 1299288 TGAAGTGCCCTTGGGGTAGAGGAGGGAAAGGCACCGCCCCATCTGGTCTCCCCCGACCCACAGCC TGAAGTGCCCTTGGGGTAGAGGAGGGAAAGGCCCCGCCCCATCTGGTCTCCCCCGACCCACAGCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1299273..1299374 32194978 MeRIP-seq:(Medium) rs71628949 Functional Loss SNV dbSNP153 33..33 33 - - - 66802 RMVar_ID_66802 Human_SNP_ID_269788 m1A Human chr1 + 1299315 1299315 1299315 AAGGCACCGCCCCATCTGGTCTCCCCCGACCCACAGCCCGCCCAGGGCCCGTGCTCACTTACCTG AAGGCACCGCCCCATCTGGTCTCCCCCGACCCTCAGCCCGCCCAGGGCCCGTGCTCACTTACCTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1299287..1299434 26863196 MeRIP-seq:(Medium) rs1360207849 Functional Loss SNV dbSNP153 33..33 33 - - - 66803 RMVar_ID_66803 Human_SNP_ID_270628 m1A Human chr1 - 1301583 1301583 1301583 GTGAGGAAGGAGGCTATGCCCAGGAGCAAAGAAAGGGCCTGGAGTGGAGGGGGGTGGGGCTGGGC GTGAGGAAGGAGGCTATGCCCAGGAGCAAAGACAGGGCCTGGAGTGGAGGGGGGTGGGGCTGGGC T G ACAP3 Ensembl:ENSG00000131584 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1301575..1301787 26863196 MeRIP-seq:(Medium) rs1394452290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8227692,Human_RBP_ID_17646218 RMVar_hsa_circ_127393,RMVar_hsa_circ_128306 66804 RMVar_ID_66804 Human_SNP_ID_271268 m1A Human chr1 + 1303194 1303194 1303194 CGAGATGACGGTGTCGCCCTGGCACTGCTGGGACAGGTCGCGGACGCCGCTCACGAAAAGCCTGC CGAGATGACGGTGTCGCCCTGGCACTGCTGGGGCAGGTCGCGGACGCCGCTCACGAAAAGCCTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1302958..1303443 32194978 MeRIP-seq:(Medium) rs866715320 Functional Loss SNV dbSNP153 33..33 33 - - - 66805 RMVar_ID_66805 Human_SNP_ID_271436 m1A Human chr1 - 1303631 1303631 1303631 GTGGAGAGGGGAGCCGTGTCCATGAGCCCCACATGGGCTGAGAAAGAGGAGGGGGCAACAGGCCG GTGGAGAGGGGAGCCGTGTCCATGAGCCCCACGTGGGCTGAGAAAGAGGAGGGGGCAACAGGCCG T C ACAP3 Ensembl:ENSG00000131584 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1303354..1303852 26863196 MeRIP-seq:(Medium) rs1470769965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3327873,Human_RBP_ID_5641342,Human_RBP_ID_8227693,Human_RBP_ID_8724552,Human_RBP_ID_9411558,Human_RBP_ID_18455306,Human_RBP_ID_19033535,Human_RBP_ID_21961009 66806 RMVar_ID_66806 Human_SNP_ID_271632 m1A Human chr1 - 1304139 1304139 1304139 ACCCCAGCCAGCCCCGTTCTTGCTTTAGGGCGACCATTGACGAGGTGGAGACGGACGTGGTGGAG ACCCCAGCCAGCCCCGTTCTTGCTTTAGGGCGGCCATTGACGAGGTGGAGACGGACGTGGTGGAG T C ACAP3 Ensembl:ENSG00000131584 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:1304055..1304226;chr1:1304014..1304248;chr1:1304076..1304256;chr1:1304051..1304229 26863196 MeRIP-seq:(Medium) rs761861299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258693,Human_RBP_ID_853429,Human_RBP_ID_18415207,Human_RBP_ID_18964421,Human_RBP_ID_22632634,Human_RBP_ID_22735254,Human_RBP_ID_23117593,Human_RBP_ID_24579554 Human_Splice_Rec_2537,Human_Splice_Rec_2580,Human_Splice_Rec_2581,Human_Splice_Rec_2712,Human_Splice_Rec_2713,Human_Splice_Rec_2730,Human_Splice_Rec_2731,Human_Splice_Rec_2746,Human_Splice_Rec_2747,Human_Splice_Rec_2756,Human_Splice_Rec_2757 66807 RMVar_ID_66807 Human_SNP_ID_274312 m1A Human chr1 + 1309842 1309840 1309843 CCCAGGCCAAGCCAGCCCCTTGGTCACCCCCGAGGAGAGCAGGTGAGGAAGGGCCCCTGGGCTGT CCCAGGCCAAGCCAGCCCCTTGGTCACCCCC___GAGAGCAGGTGAGGAAGGGCCCCTGGGCTGT CGAG C PUSL1 Ensembl:ENSG00000169972 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1309741..1309842 26863410 MeRIP-seq:(Medium) rs1189795058 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_2767,Human_Splice_Rec_2779,Human_Splice_Rec_2791 66808 RMVar_ID_66808 Human_SNP_ID_275937 m1A Human chr1 + 1312365 1312365 1312365 TTTGAGGGCTTGCTCTGAGGACACCAGCCGGAAGTTCTGTGGGGCAGGGACAGGTCAGTGAGCGC TTTGAGGGCTTGCTCTGAGGACACCAGCCGGACGTTCTGTGGGGCAGGGACAGGTCAGTGAGCGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1311070..1313400 32194978 MeRIP-seq:(Medium) rs1288242742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1724023,Human_RBP_ID_5681292,Human_RBP_ID_22126023 66809 RMVar_ID_66809 Human_SNP_ID_276162 m1A Human chr1 - 1312702 1312701 1312702 CTGGGCTGAGGCTCTCTCTTCCCCCGGGGTCCAGGGGTCAACTGCTACATGCCGGCCAATGGCGA CTGGGCTGAGGCTCTCTCTTCCCCCGGGGTCC_GGGGTCAACTGCTACATGCCGGCCAATGGCGA CT C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1312676..1312725 26863196 MeRIP-seq:(Medium) rs781730758 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_852117 RMVar_hsa_circ_28672,RMVar_hsa_circ_117602,RMVar_hsa_circ_128309,RMVar_hsa_circ_20795 66810 RMVar_ID_66810 Human_SNP_ID_276163 m1A Human chr1 - 1312702 1312702 1312702 CTGGGCTGAGGCTCTCTCTTCCCCCGGGGTCCAGGGGTCAACTGCTACATGCCGGCCAATGGCGA CTGGGCTGAGGCTCTCTCTTCCCCCGGGGTCCGGGGGTCAACTGCTACATGCCGGCCAATGGCGA T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1312676..1312725 26863196 MeRIP-seq:(Medium) rs1023476244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_852117 RMVar_hsa_circ_28672,RMVar_hsa_circ_117602,RMVar_hsa_circ_128309,RMVar_hsa_circ_20795 66811 RMVar_ID_66811 Human_SNP_ID_276348 m1A Human chr1 + 1313029 1313029 1313029 CCTCGGCCCTGCCAGCCCAGTGCGGGGTCGAGACTCACCACCTGCCGCCCCTCCATCTCGAGCTT CCTCGGCCCTGCCAGCCCAGTGCGGGGTCGAGTCTCACCACCTGCCGCCCCTCCATCTCGAGCTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1313026..1313125 26863196 MeRIP-seq:(Medium) rs750983730 Functional Loss SNV dbSNP153 33..33 33 - - - 66812 RMVar_ID_66812 Human_SNP_ID_277679 m1A Human chr1 - 1315872 1315872 1315872 GCTGTGTGTGAGCAACAGGGACTGAAAAGCTCAGTGCAGTGCCCTCGCTCCCCGCCCCGCCTCCC GCTGTGTGTGAGCAACAGGGACTGAAAAGCTCGGTGCAGTGCCCTCGCTCCCCGCCCCGCCTCCC T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1315869..1315952 26863196 MeRIP-seq:(Medium) rs1042513345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1071364,Human_RBP_ID_10553734,Human_RBP_ID_23328039 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 66813 RMVar_ID_66813 Human_SNP_ID_277682 m1A Human chr1 - 1315888 1315886 1315888 CCCTTGTGAACTGGATGCTGTGTGTGAGCAACAGGGACTGAAAAGCTCAGTGCAGTGCCCTCGCT CCCTTGTGAACTGGATGCTGTGTGTGAGCAAC__GGACTGAAAAGCTCAGTGCAGTGCCCTCGCT CCT C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1315837..1315983 26863196 MeRIP-seq:(Medium) rs1475199169 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1071364,Human_RBP_ID_1149088,Human_RBP_ID_1409972,Human_RBP_ID_8283240,Human_RBP_ID_10553734,Human_RBP_ID_18549581,Human_RBP_ID_18929072,Human_RBP_ID_23328040 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 66814 RMVar_ID_66814 Human_SNP_ID_278020 m1A Human chr1 + 1316868 1316868 1316868 ACTGCTTGAACCCGGGAGGCGGAGGTTGCAGTAAGCCGAGATCGCGCCACTGCACTCCAGCCTGG ACTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGG A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs376482516 Functional Loss SNV dbSNP153 33..33 33 - - - 66815 RMVar_ID_66815 Human_SNP_ID_279015 m1A Human chr1 - 1319522 1319522 1319522 CCCAGGCTGACCTGTGCTGCGTCCCCCTAGCCACTTCCACCTGGACCACTGCGGGGCACTCCCCT CCCAGGCTGACCTGTGCTGCGTCCCCCTAGCCCCTTCCACCTGGACCACTGCGGGGCACTCCCCT T G INTS11 Ensembl:ENSG00000127054 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:1319357..1319562;chr1:1318811..1319559;chr1:1319276..1319567;chr1:1319351..1319574 26863196 MeRIP-seq:(Medium) rs756831865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934857,Human_RBP_ID_9357811,Human_RBP_ID_17674826 Human_Splice_Rec_2826,Human_Splice_Rec_2860,Human_Splice_Rec_2918,Human_Splice_Rec_2970,Human_Splice_Rec_3092,Human_Splice_Rec_3176,Human_Splice_Rec_3210,Human_Splice_Rec_3268,Human_Splice_Rec_3342,Human_Splice_Rec_3362,Human_Splice_Rec_3382,Human_Splice_Rec_3398,Human_Splice_Rec_3412,Human_Splice_Rec_3426,Human_Splice_Rec_3440,Human_Splice_Rec_3448,Human_Splice_Rec_3452,Human_Splice_Rec_3466,Human_Splice_Rec_3484,Human_Splice_Rec_3494 RMVar_hsa_circ_28672,RMVar_hsa_circ_25202,RMVar_hsa_circ_55849,RMVar_hsa_circ_128313,RMVar_hsa_circ_77492,RMVar_hsa_circ_332407 66816 RMVar_ID_66816 Human_SNP_ID_279354 m1A Human chr1 - 1320531 1320519 1320532 ACTGTGCAACCTGAAACCCCCACATCCTTCCTAGCGACGCTTCCCTGACTTCTCCTACATCACCC ACTGTGCAACCTGAAACCCCCACATCCTTCC_____________CTGACTTCTCCTACATCACCC GGGAAGCGTCGCTA G INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr1:1320451..1320603;chr1:1320451..1320700;chr1:1320455..1320755 26863410,26863196,32194978 MeRIP-seq:(Medium) rs1262901513 Functional Loss DEL dbSNP153 32..44 33 - - - Human_RBP_ID_19040654,Human_RBP_ID_22786763 Human_Splice_Rec_2825,Human_Splice_Rec_2859,Human_Splice_Rec_2917,Human_Splice_Rec_2937,Human_Splice_Rec_2969,Human_Splice_Rec_3091,Human_Splice_Rec_3175,Human_Splice_Rec_3209,Human_Splice_Rec_3267,Human_Splice_Rec_3341,Human_Splice_Rec_3361,Human_Splice_Rec_3373,Human_Splice_Rec_3397,Human_Splice_Rec_3411,Human_Splice_Rec_3425,Human_Splice_Rec_3439,Human_Splice_Rec_3447,Human_Splice_Rec_3451,Human_Splice_Rec_3459,Human_Splice_Rec_3465,Human_Splice_Rec_3471,Human_Splice_Rec_3477,Human_Splice_Rec_3483,Human_Splice_Rec_3493,Human_Splice_Rec_3499 RMVar_hsa_circ_25202,RMVar_hsa_circ_55849,RMVar_hsa_circ_332407 66817 RMVar_ID_66817 Human_SNP_ID_279535 m1A Human chr1 - 1320925 1320925 1320925 CCGGCCATCCACAGCTGGACCCTGGGCCTCAGAGCCGGGACAGTGGGGTGGTGGGCAGCAGTGGT CCGGCCATCCACAGCTGGACCCTGGGCCTCAGTGCCGGGACAGTGGGGTGGTGGGCAGCAGTGGT T A INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1320921..1321140 26863196 MeRIP-seq:(Medium) rs775166112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17098914,Human_RBP_ID_19042498 RMVar_hsa_circ_25202,RMVar_hsa_circ_55849,RMVar_hsa_circ_332407 66818 RMVar_ID_66818 Human_SNP_ID_279593 m1A Human chr1 - 1321042 1321042 1321042 CCGAAGCTGCATCCTGGTCTCCATTGCGGGCAAGAATGTCATGCTGGACTGTGGAATGCACATGG CCGAAGCTGCATCCTGGTCTCCATTGCGGGCAGGAATGTCATGCTGGACTGTGGAATGCACATGG T C INTS11 Ensembl:ENSG00000127054 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1320835..1321915 26863196 MeRIP-seq:(Medium) rs745666726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24732,Human_RBP_ID_323915,Human_RBP_ID_1149102,Human_RBP_ID_1410006,Human_RBP_ID_1724046,Human_RBP_ID_3279211,Human_RBP_ID_4073399,Human_RBP_ID_9357812,Human_RBP_ID_10554064,Human_RBP_ID_18549616,Human_RBP_ID_23328086,Human_RBP_ID_26839707 Human_Splice_Rec_2822,Human_Splice_Rec_2823,Human_Splice_Rec_2856,Human_Splice_Rec_2857,Human_Splice_Rec_2914,Human_Splice_Rec_2915,Human_Splice_Rec_2936,Human_Splice_Rec_2966,Human_Splice_Rec_2967,Human_Splice_Rec_3088,Human_Splice_Rec_3089,Human_Splice_Rec_3120,Human_Splice_Rec_3121,Human_Splice_Rec_3148,Human_Splice_Rec_3149,Human_Splice_Rec_3172,Human_Splice_Rec_3173,Human_Splice_Rec_3206,Human_Splice_Rec_3207,Human_Splice_Rec_3264,Human_Splice_Rec_3265,Human_Splice_Rec_3338,Human_Splice_Rec_3339,Human_Splice_Rec_3358,Human_Splice_Rec_3359,Human_Splice_Rec_3370,Human_Splice_Rec_3371,Human_Splice_Rec_3394,Human_Splice_Rec_3395,Human_Splice_Rec_3408,Human_Splice_Rec_3409,Human_Splice_Rec_3422,Human_Splice_Rec_3423,Human_Splice_Rec_3444,Human_Splice_Rec_3445,Human_Splice_Rec_3450,Human_Splice_Rec_3454,Human_Splice_Rec_3456,Human_Splice_Rec_3457,Human_Splice_Rec_3462,Human_Splice_Rec_3463,Human_Splice_Rec_3468,Human_Splice_Rec_3469,Human_Splice_Rec_3474,Human_Splice_Rec_3475,Human_Splice_Rec_3480,Human_Splice_Rec_3481,Human_Splice_Rec_3490,Human_Splice_Rec_3491,Human_Splice_Rec_3496,Human_Splice_Rec_3497,Human_Splice_Rec_3504,Human_Splice_Rec_3505 Human_miRNA_ID_158576,Human_miRNA_ID_968258,Human_miRNA_ID_1079146,Human_miRNA_ID_1327818 RMVar_hsa_circ_25202,RMVar_hsa_circ_55849,RMVar_hsa_circ_332407 66819 RMVar_ID_66819 Human_SNP_ID_280674 m1A Human chr1 - 1323977 1323945 1323978 AGACCCTCAGTCCCCCAGCCCCTCAGTCCCCCAGCCCCTCAGCCCAGCAGACCCCCAGACCCTCA AGACCCTCAGTCCCCCAGCCCCTCAGTCCCC_________________________________A TGAGGGTCTGGGGGTCTGCTGGGCTGAGGGGCTG T INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1323975..1324046 26863196 MeRIP-seq:(Medium) rs1386411028 Functional Loss DEL dbSNP153 32..64 33 - - - Human_RBP_ID_17072102,Human_RBP_ID_26773752 RMVar_hsa_circ_25202 66820 RMVar_ID_66820 Human_SNP_ID_280933 m1A Human chr1 + 1324239 1324239 1324239 GCTGAGGGTCTGCGGGGCTGAGGGGCTAAGGGACTGAAGGGCTGGTAGGGCTGGAGGCGGCAGCG GCTGAGGGTCTGCGGGGCTGAGGGGCTAAGGGGCTGAAGGGCTGGTAGGGCTGGAGGCGGCAGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1324237..1324650 26863196 MeRIP-seq:(Medium) rs1192516884 Functional Loss SNV dbSNP153 33..33 33 - - - 66821 RMVar_ID_66821 Human_SNP_ID_281028 m1A Human chr1 + 1324465 1324465 1324465 TCCCACCAGGGCCCGCGCGGGGAGGAGACCGGAGGACGCCCGCGGCGCGCACCTGGCTCCACGAG TCCCACCAGGGCCCGCGCGGGGAGGAGACCGGCGGACGCCCGCGGCGCGCACCTGGCTCCACGAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1324459..1324600 26863196 MeRIP-seq:(Medium) rs897990179 Functional Loss SNV dbSNP153 33..33 33 - - - 66822 RMVar_ID_66822 Human_SNP_ID_281029 m1A Human chr1 + 1324465 1324465 1324465 TCCCACCAGGGCCCGCGCGGGGAGGAGACCGGAGGACGCCCGCGGCGCGCACCTGGCTCCACGAG TCCCACCAGGGCCCGCGCGGGGAGGAGACCGGGGGACGCCCGCGGCGCGCACCTGGCTCCACGAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1324459..1324600 26863196 MeRIP-seq:(Medium) rs897990179 Functional Loss SNV dbSNP153 33..33 33 - - - 66823 RMVar_ID_66823 Human_SNP_ID_281326 m1A Human chr1 + 1324855 1324855 1324855 GCCTAGGTGAGCGGCTCGGACTCGGCGGCCGCACCTGCCCAACCCAACCCGCACGGTCCGGAAGT GCCTAGGTGAGCGGCTCGGACTCGGCGGCCGCGCCTGCCCAACCCAACCCGCACGGTCCGGAAGT A G CPTP Ensembl:ENSG00000224051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1324849..1325034 26863196 MeRIP-seq:(Medium) rs933656837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3988441 RMVar_hsa_circ_128314,RMVar_hsa_circ_96995 66824 RMVar_ID_66824 Human_SNP_ID_281327 m1A Human chr1 + 1324855 1324855 1324855 GCCTAGGTGAGCGGCTCGGACTCGGCGGCCGCACCTGCCCAACCCAACCCGCACGGTCCGGAAGT GCCTAGGTGAGCGGCTCGGACTCGGCGGCCGCTCCTGCCCAACCCAACCCGCACGGTCCGGAAGT A T CPTP Ensembl:ENSG00000224051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1324849..1325034 26863196 MeRIP-seq:(Medium) rs933656837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3988441 RMVar_hsa_circ_128314,RMVar_hsa_circ_96995 66825 RMVar_ID_66825 Human_SNP_ID_282247 m1A Human chr1 + 1327545 1327542 1327545 CACGCACCTCCGCGCTCTGCGCCGACTCCTACAACGCCTCGCTGGCCGCCTACCACCCCTGGGTC CACGCACCTCCGCGCTCTGCGCCGACTCCT___ACGCCTCGCTGGCCGCCTACCACCCCTGGGTC TACA T CPTP Ensembl:ENSG00000224051 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1327496..1327666 26863196 MeRIP-seq:(Medium) rs745942142 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3988490,Human_RBP_ID_5336513 RMVar_hsa_circ_128314,RMVar_hsa_circ_96995 66826 RMVar_ID_66826 Human_SNP_ID_282249 m1A Human chr1 + 1327545 1327545 1327545 CACGCACCTCCGCGCTCTGCGCCGACTCCTACAACGCCTCGCTGGCCGCCTACCACCCCTGGGTC CACGCACCTCCGCGCTCTGCGCCGACTCCTACTACGCCTCGCTGGCCGCCTACCACCCCTGGGTC A T CPTP Ensembl:ENSG00000224051 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1327496..1327666 26863196 MeRIP-seq:(Medium) rs769624517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3988490,Human_RBP_ID_5336513 RMVar_hsa_circ_128314,RMVar_hsa_circ_96995 66827 RMVar_ID_66827 Human_SNP_ID_286316 m1A Human chr1 + 1335402 1335402 1335402 TACAGTATCTACAGCACAGACACGTGGGGGCCAGAGAAGCCAGGAAGGCCGCGATGTGTGCGCGC TACAGTATCTACAGCACAGACACGTGGGGGCCCGAGAAGCCAGGAAGGCCGCGATGTGTGCGCGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1335352..1335480 26863196 MeRIP-seq:(Medium) rs1282592571 Functional Loss SNV dbSNP153 33..33 33 - - - 66828 RMVar_ID_66828 Human_SNP_ID_286474 m1A Human chr1 - 1335744 1335744 1335744 GTGCACAGGCCCCCTGTCTGGAGTAGGGATCTAATTTATTTATTTATTGCCTGGCCGGTGACTCG GTGCACAGGCCCCCTGTCTGGAGTAGGGATCTTATTTATTTATTTATTGCCTGGCCGGTGACTCG T A DVL1 Ensembl:ENSG00000107404 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1335351..1336167 32194978 MeRIP-seq:(Medium) rs1482592170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323954,Human_RBP_ID_5681531,Human_RBP_ID_17723737,Human_RBP_ID_18216032 RMVar_hsa_circ_98157,RMVar_hsa_circ_120031,RMVar_hsa_circ_128315,RMVar_hsa_circ_128316 66829 RMVar_ID_66829 Human_SNP_ID_286795 m1A Human chr1 + 1336352 1336352 1336352 GTAGCCGAGGCCTGACTGCGTGGGCTGCTGCCACGGCTGAGCTGGCCGGCCGGACGCTCTCGCCA GTAGCCGAGGCCTGACTGCGTGGGCTGCTGCCGCGGCTGAGCTGGCCGGCCGGACGCTCTCGCCA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1336303..1336475 26863196 MeRIP-seq:(Medium) rs1396021822 Functional Loss SNV dbSNP153 33..33 33 - - - 66830 RMVar_ID_66830 Human_SNP_ID_286852 m1A Human chr1 + 1336420 1336420 1336420 GCTCCCCACCCCACTCGGTGCCGTGTGATCCGATTCACTGCCACTGCCCCCAGCTCCCGCCGCCC GCTCCCCACCCCACTCGGTGCCGTGTGATCCGCTTCACTGCCACTGCCCCCAGCTCCCGCCGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1336182..1336535 26863196 MeRIP-seq:(Medium) rs1410707213 Functional Loss SNV dbSNP153 33..33 33 - - - 66831 RMVar_ID_66831 Human_SNP_ID_287264 m1A Human chr1 - 1337245 1337243 1337246 CGTGGAGGGCCCAGGAAGGAGGGCGAGAGAGGAGAGGCGGCCAGAGGGTGTGGGACCGCAGAGAA CGTGGAGGGCCCAGGAAGGAGGGCGAGAGAG___AGGCGGCCAGAGGGTGTGGGACCGCAGAGAA TCTC T DVL1 Ensembl:ENSG00000107404 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1337243..1337356 26863196 MeRIP-seq:(Medium) rs1466542171 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3329228,Human_RBP_ID_5312151,Human_RBP_ID_5332492,Human_RBP_ID_8051341,Human_RBP_ID_9411569,Human_RBP_ID_19042502,Human_RBP_ID_22632648 RMVar_hsa_circ_98157,RMVar_hsa_circ_120031,RMVar_hsa_circ_128315,RMVar_hsa_circ_128316 66832 RMVar_ID_66832 Human_SNP_ID_287954 m1A Human chr1 - 1338370 1338370 1338370 GGAGGGCTTCAAGGAGCGGCGGGAGGCCCGGAAGTACGCCAGCAGCTTGCTGAAGCACGGCTTCC GGAGGGCTTCAAGGAGCGGCGGGAGGCCCGGAGGTACGCCAGCAGCTTGCTGAAGCACGGCTTCC T C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1338319..1338507 26863196 MeRIP-seq:(Medium) rs1259994994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934863,Human_RBP_ID_18966777,Human_RBP_ID_22871120 Human_Splice_Rec_3552,Human_Splice_Rec_3580,Human_Splice_Rec_3602,Human_Splice_Rec_3618,Human_Splice_Rec_3630 RMVar_hsa_circ_26266,RMVar_hsa_circ_98157,RMVar_hsa_circ_120031,RMVar_hsa_circ_128315,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_35273,RMVar_hsa_circ_35300,RMVar_hsa_circ_88949,RMVar_hsa_circ_128317,RMVar_hsa_circ_128318 66833 RMVar_ID_66833 Human_SNP_ID_288706 m1A Human chr1 + 1339747 1339747 1339747 TCCAGCGCCCCCAGCCCTCACCCCGTCTGGGAAACGATCTCCCGCAGCACCCGCACGGCATCGTC TCCAGCGCCCCCAGCCCTCACCCCGTCTGGGACACGATCTCCCGCAGCACCCGCACGGCATCGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1339557..1339867 26863196 MeRIP-seq:(Medium) rs765422342 Functional Loss SNV dbSNP153 33..33 33 - - - 66834 RMVar_ID_66834 Human_SNP_ID_288707 m1A Human chr1 + 1339747 1339747 1339747 TCCAGCGCCCCCAGCCCTCACCCCGTCTGGGAAACGATCTCCCGCAGCACCCGCACGGCATCGTC TCCAGCGCCCCCAGCCCTCACCCCGTCTGGGAGACGATCTCCCGCAGCACCCGCACGGCATCGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1339557..1339867 26863196 MeRIP-seq:(Medium) rs765422342 Functional Loss SNV dbSNP153 33..33 33 - - - 66835 RMVar_ID_66835 Human_SNP_ID_288891 m1A Human chr1 + 1340028 1340028 1340028 CACCCGCAGCTACATGTCACCCCGCAGCCCCCACAGACACACCTGCAGCAACATGTCGCCGGGCT CACCCGCAGCTACATGTCACCCCGCAGCCCCCCCAGACACACCTGCAGCAACATGTCGCCGGGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1340026..1340050 26863196 MeRIP-seq:(Medium) rs756600009 Functional Loss SNV dbSNP153 33..33 33 - - - 66836 RMVar_ID_66836 Human_SNP_ID_288892 m1A Human chr1 + 1340028 1340028 1340028 CACCCGCAGCTACATGTCACCCCGCAGCCCCCACAGACACACCTGCAGCAACATGTCGCCGGGCT CACCCGCAGCTACATGTCACCCCGCAGCCCCCGCAGACACACCTGCAGCAACATGTCGCCGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1340026..1340050 26863196 MeRIP-seq:(Medium) rs756600009 Functional Loss SNV dbSNP153 33..33 33 - - - 66837 RMVar_ID_66837 Human_SNP_ID_288946 m1A Human chr1 + 1340107 1340107 1340107 GCGGCCACAGCCCCGCCCTTCATGATGGAGCCAATGTAGATGCCGCCGTCTCCACGGTCGTTGCT GCGGCCACAGCCCCGCCCTTCATGATGGAGCCGATGTAGATGCCGCCGTCTCCACGGTCGTTGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1340026..1340113 26863196 MeRIP-seq:(Medium) rs1178080502 Functional Loss SNV dbSNP153 33..33 33 - - - 66838 RMVar_ID_66838 Human_SNP_ID_288963 m1A Human chr1 - 1340135 1340133 1340136 CTTTCTGGGCATCAGCATCGTGGGGCAGAGCAACGACCGTGGAGACGGCGGCATCTACATTGGCT CTTTCTGGGCATCAGCATCGTGGGGCAGAGC___GACCGTGGAGACGGCGGCATCTACATTGGCT CGTT C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1340036..1340233 26863196 MeRIP-seq:(Medium) rs770209968 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_741817,Human_RBP_ID_3934867,Human_RBP_ID_3988681,Human_RBP_ID_5108947,Human_RBP_ID_9269544,Human_RBP_ID_9357815,Human_RBP_ID_22779471,Human_RBP_ID_26309973,Human_RBP_ID_27387146 Human_Splice_Rec_3542,Human_Splice_Rec_3543,Human_Splice_Rec_3570,Human_Splice_Rec_3571,Human_Splice_Rec_3609,Human_Splice_Rec_3623,Human_Splice_Rec_3632,Human_Splice_Rec_3633 RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_32455,RMVar_hsa_circ_128317,RMVar_hsa_circ_23178 66839 RMVar_ID_66839 Human_SNP_ID_289101 m1A Human chr1 + 1340326 1340324 1340326 GTTATGCTGCTGAAGGAGGAGGCCTATGGAGGAGAGGGGGCGTGTGTAAAAGGCACGGGGCTGCC GTTATGCTGCTGAAGGAGGAGGCCTATGGAG__GAGGGGGCGTGTGTAAAAGGCACGGGGCTGCC GGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1340324..1340415 26863196 MeRIP-seq:(Medium) rs1557667753 Functional Loss DEL dbSNP153 32..33 33 - - - 66840 RMVar_ID_66840 Human_SNP_ID_290169 m1A Human chr1 + 1341754 1341754 1341754 TGCTGAGGGCGGTGGACGCGCTGTCTGGGGGCAGCCCCACATCCCGCCGTCGGTCTCCCCTTGGG TGCTGAGGGCGGTGGACGCGCTGTCTGGGGGCGGCCCCACATCCCGCCGTCGGTCTCCCCTTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1341633..1341856 26863196 MeRIP-seq:(Medium) rs926069678 Functional Loss SNV dbSNP153 33..33 33 - - - 66841 RMVar_ID_66841 Human_SNP_ID_290191 m1A Human chr1 - 1341782 1341782 1341782 CCCCCACAGCCGCCCGGACCAATGGGCACCCAAGGGGAGACCGACGGCGGGATGTGGGGCTGCCC CCCCCACAGCCGCCCGGACCAATGGGCACCCAGGGGGAGACCGACGGCGGGATGTGGGGCTGCCC T C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1341672..1341834 26863196 MeRIP-seq:(Medium) rs376205129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3988689,Human_RBP_ID_5432789,Human_RBP_ID_5484170 Human_Splice_Rec_3536,Human_Splice_Rec_3564,Human_Splice_Rec_3592 RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_121380,RMVar_hsa_circ_32455,RMVar_hsa_circ_128317,RMVar_hsa_circ_23178,RMVar_hsa_circ_372589,RMVar_hsa_circ_128321,RMVar_hsa_circ_128322 66842 RMVar_ID_66842 Human_SNP_ID_290192 m1A Human chr1 - 1341782 1341782 1341782 CCCCCACAGCCGCCCGGACCAATGGGCACCCAAGGGGAGACCGACGGCGGGATGTGGGGCTGCCC CCCCCACAGCCGCCCGGACCAATGGGCACCCACGGGGAGACCGACGGCGGGATGTGGGGCTGCCC T G DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1341672..1341834 26863196 MeRIP-seq:(Medium) rs376205129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3988689,Human_RBP_ID_5432789,Human_RBP_ID_5484170 Human_Splice_Rec_3536,Human_Splice_Rec_3564,Human_Splice_Rec_3592 RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_121380,RMVar_hsa_circ_32455,RMVar_hsa_circ_128317,RMVar_hsa_circ_23178,RMVar_hsa_circ_372589,RMVar_hsa_circ_128321,RMVar_hsa_circ_128322 66843 RMVar_ID_66843 Human_SNP_ID_290371 m1A Human chr1 - 1342158 1342158 1342158 CGGCCTCCCCACCCACCCTGCTCTTGTTGCACAGCCCAAATGTGGCCAGCAGCCGTGACGGGATG CGGCCTCCCCACCCACCCTGCTCTTGTTGCACGGCCCAAATGTGGCCAGCAGCCGTGACGGGATG T C DVL1 Ensembl:ENSG00000107404 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1342051..1349053 32194978 MeRIP-seq:(Medium) rs1377480264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_121380,RMVar_hsa_circ_372589,RMVar_hsa_circ_128321,RMVar_hsa_circ_128322 66844 RMVar_ID_66844 Human_SNP_ID_290907 m1A Human chr1 + 1343282 1343282 1343282 GCTTGGAGCCCCCCCCCCCCAGGGCTTCCCCCACACTGGGACTCCTCAGGGCCAGGCCCCAGCCT GCTTGGAGCCCCCCCCCCCCAGGGCTTCCCCCCCACTGGGACTCCTCAGGGCCAGGCCCCAGCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1343277..1343499 26863196 MeRIP-seq:(Medium) rs1193581546 Functional Loss SNV dbSNP153 33..33 33 - - - 66845 RMVar_ID_66845 Human_SNP_ID_290908 m1A Human chr1 + 1343282 1343282 1343282 GCTTGGAGCCCCCCCCCCCCAGGGCTTCCCCCACACTGGGACTCCTCAGGGCCAGGCCCCAGCCT GCTTGGAGCCCCCCCCCCCCAGGGCTTCCCCCTCACTGGGACTCCTCAGGGCCAGGCCCCAGCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1343277..1343499 26863196 MeRIP-seq:(Medium) rs1193581546 Functional Loss SNV dbSNP153 33..33 33 - - - 66846 RMVar_ID_66846 Human_SNP_ID_290912 m1A Human chr1 + 1343310 1343310 1343310 CCCCACACTGGGACTCCTCAGGGCCAGGCCCCAGCCTCCTCAGCAGCAGCAGCTGCACCTACCGG CCCCACACTGGGACTCCTCAGGGCCAGGCCCCCGCCTCCTCAGCAGCAGCAGCTGCACCTACCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1343306..1343488 26863196 MeRIP-seq:(Medium) rs1170668534 Functional Loss SNV dbSNP153 33..33 33 - - - 66847 RMVar_ID_66847 Human_SNP_ID_290913 m1A Human chr1 + 1343310 1343310 1343310 CCCCACACTGGGACTCCTCAGGGCCAGGCCCCAGCCTCCTCAGCAGCAGCAGCTGCACCTACCGG CCCCACACTGGGACTCCTCAGGGCCAGGCCCCGGCCTCCTCAGCAGCAGCAGCTGCACCTACCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1343306..1343488 26863196 MeRIP-seq:(Medium) rs1170668534 Functional Loss SNV dbSNP153 33..33 33 - - - 66848 RMVar_ID_66848 Human_SNP_ID_292934 m1A Human chr1 - 1349252 1349252 1349252 GGGCGGCCGCGGGCCGCGGGGCAGCAGTCGGGACGCGCGCGGGAGCCGGGGGCGGCGGCCGGGGC GGGCGGCCGCGGGCCGCGGGGCAGCAGTCGGGGCGCGCGCGGGAGCCGGGGGCGGCGGCCGGGGC T C DVL1 Ensembl:ENSG00000107404 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1348849..1349450 26863196 MeRIP-seq:(Medium) rs1285810661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223630,Human_RBP_ID_4072400,Human_RBP_ID_9318420,Human_RBP_ID_9352448,Human_RBP_ID_21961032,Human_RBP_ID_26773768 66849 RMVar_ID_66849 Human_SNP_ID_292969 m1A Human chr1 - 1349351 1349351 1349351 TTTAACGGCGCGGCCCGAGGGGCGCAGGCGGGAGGGCGGCGGGGCTGAGCGCGCCCTCCGTGCTG TTTAACGGCGCGGCCCGAGGGGCGCAGGCGGGGGGGCGGCGGGGCTGAGCGCGCCCTCCGTGCTG T C DVL1 Ensembl:ENSG00000107404 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1342717..1349400 26863196 MeRIP-seq:(Medium) rs1004676729 Functional Loss SNV dbSNP153 33..33 33 - - - 66850 RMVar_ID_66850 Human_SNP_ID_293220 m1A Human chr1 + 1349856 1349856 1349856 TGGGGTTCTCCGCAGGGCAGGGGAGACTTCCGAGGCGTCCCTTGAGGCCGCGGGGCGTCCGCGCT TGGGGTTCTCCGCAGGGCAGGGGAGACTTCCGCGGCGTCCCTTGAGGCCGCGGGGCGTCCGCGCT A C HSALNG0000138 RNACentral:URS0000EBB5B0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1349596..1350000;chr1:1349621..1350005 26863196 MeRIP-seq:(Medium) rs1259797728 Functional Loss SNV dbSNP153 33..33 33 - - - 66851 RMVar_ID_66851 Human_SNP_ID_295256 m1A Human chr1 - 1355282 1355282 1355282 CTGCAACCTGCACCATCACTACTGCCACCTCTACGAGAGCCTGGCCGTCCGCCTGGAGGTCACCG CTGCAACCTGCACCATCACTACTGCCACCTCTTCGAGAGCCTGGCCGTCCGCCTGGAGGTCACCG T A MXRA8 Ensembl:ENSG00000162576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1355261..1355609 32194978 MeRIP-seq:(Medium) rs779739924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_3650,Human_Splice_Rec_3651,Human_Splice_Rec_3668,Human_Splice_Rec_3669,Human_Splice_Rec_3686,Human_Splice_Rec_3687,Human_Splice_Rec_3704,Human_Splice_Rec_3705,Human_Splice_Rec_3736,Human_Splice_Rec_3737 RMVar_hsa_circ_50994,RMVar_hsa_circ_123393,RMVar_hsa_circ_128323 66852 RMVar_ID_66852 Human_SNP_ID_295257 m1A Human chr1 - 1355282 1355282 1355282 CTGCAACCTGCACCATCACTACTGCCACCTCTACGAGAGCCTGGCCGTCCGCCTGGAGGTCACCG CTGCAACCTGCACCATCACTACTGCCACCTCTGCGAGAGCCTGGCCGTCCGCCTGGAGGTCACCG T C MXRA8 Ensembl:ENSG00000162576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1355261..1355609 32194978 MeRIP-seq:(Medium) rs779739924 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_3650,Human_Splice_Rec_3651,Human_Splice_Rec_3668,Human_Splice_Rec_3669,Human_Splice_Rec_3686,Human_Splice_Rec_3687,Human_Splice_Rec_3704,Human_Splice_Rec_3705,Human_Splice_Rec_3736,Human_Splice_Rec_3737 RMVar_hsa_circ_50994,RMVar_hsa_circ_123393,RMVar_hsa_circ_128323 66853 RMVar_ID_66853 Human_SNP_ID_295368 m1A Human chr1 + 1355448 1355448 1355448 CCGACCCCGCGGCCCCGGTCCCCGGTCCCCGCACCGCGGATGAGCAGCGAGAAGTTGCCGTCGTC CCGACCCCGCGGCCCCGGTCCCCGGTCCCCGCCCCGCGGATGAGCAGCGAGAAGTTGCCGTCGTC A C NONHSAG000093.2 RNACentral:URS00009C1BE2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1355444..1355703 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 66854 RMVar_ID_66854 Human_SNP_ID_295850 m1A Human chr1 + 1356437 1356437 1356437 GGGGGCATCTGTGGGGGAGGGGTGGGCCCCCGAGGGCCCTGGTGGGTGTGCGGGAGTCTGTGGGG GGGGGCATCTGTGGGGGAGGGGTGGGCCCCCGGGGGCCCTGGTGGGTGTGCGGGAGTCTGTGGGG A G NONHSAG000093.2,NONHSAG000093.2:2 RNACentral:URS00008C2676,RNACentral:URS00009C1BE2 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1356431..1356549 26863196 MeRIP-seq:(Medium) rs1432700842 Functional Loss SNV dbSNP153 33..33 33 - - - 66855 RMVar_ID_66855 Human_SNP_ID_295865 m1A Human chr1 + 1356471 1356470 1356471 GGCCCTGGTGGGTGTGCGGGAGTCTGTGGGGGAGGGCCAGGCCCCCAAGGGCCCTGGTAGGGGAA GGCCCTGGTGGGTGTGCGGGAGTCTGTGGGGG_GGGCCAGGCCCCCAAGGGCCCTGGTAGGGGAA GA G NONHSAG000093.2,NONHSAG000093.2:2 RNACentral:URS00008C2676,RNACentral:URS00009C1BE2 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1356466..1356538 26863196 MeRIP-seq:(Medium) rs1164984562 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2090866 66856 RMVar_ID_66856 Human_SNP_ID_295867 m1A Human chr1 + 1356471 1356471 1356471 GGCCCTGGTGGGTGTGCGGGAGTCTGTGGGGGAGGGCCAGGCCCCCAAGGGCCCTGGTAGGGGAA GGCCCTGGTGGGTGTGCGGGAGTCTGTGGGGGGGGGCCAGGCCCCCAAGGGCCCTGGTAGGGGAA A G NONHSAG000093.2,NONHSAG000093.2:2 RNACentral:URS00008C2676,RNACentral:URS00009C1BE2 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1356466..1356538 26863196 MeRIP-seq:(Medium) rs1387873717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2090866 66857 RMVar_ID_66857 Human_SNP_ID_296196 m1A Human chr1 + 1357299 1357299 1357299 CTCTGAATCTAGGCTGGACTTTCTCTGACCGGAAGCGGGGCTGCCACCCGGGACAGTTTCCAATT CTCTGAATCTAGGCTGGACTTTCTCTGACCGGCAGCGGGGCTGCCACCCGGGACAGTTTCCAATT A C NONHSAG000093.2,NONHSAG000093.2:2 RNACentral:URS00008C2676,RNACentral:URS00009C1BE2 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1357294..1357379 26863196 MeRIP-seq:(Medium) rs1470003739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17723754 66858 RMVar_ID_66858 Human_SNP_ID_297635 m1A Human chr1 + 1361054 1361053 1361055 ACACATGCATGCACATGAAGACACGGAGACACAGATACATGGAAACACGAACACAGACATGCGCA ACACATGCATGCACATGAAGACACGGAGACAC__ATACATGGAAACACGAACACAGACATGCGCA CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1361049..1361120 26863196 MeRIP-seq:(Medium) rs199723493 Functional Loss DEL dbSNP153 33..34 33 - - - 66859 RMVar_ID_66859 Human_SNP_ID_302644 m1A Human chr1 - 1374115 1374115 1374115 AGGCGTCGCGGATGCGCCTCAAATTCAGTGCAAAAACGTGCTGAAGATCCGCCGGCGGAAGATGA AGGCGTCGCGGATGCGCCTCAAATTCAGTGCAGAAACGTGCTGAAGATCCGCCGGCGGAAGATGA T C AURKAIP1 Ensembl:ENSG00000175756 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:1373778..1374175;chr1:1373778..1374465 32194978 MeRIP-seq:(Medium) rs781737581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323996,Human_RBP_ID_970538,Human_RBP_ID_5136575,Human_RBP_ID_10554281,Human_RBP_ID_18468411,Human_RBP_ID_22024523,Human_RBP_ID_22426812,Human_RBP_ID_23328308,Human_RBP_ID_26839822 66860 RMVar_ID_66860 Human_SNP_ID_302645 m1A Human chr1 - 1374115 1374115 1374115 AGGCGTCGCGGATGCGCCTCAAATTCAGTGCAAAAACGTGCTGAAGATCCGCCGGCGGAAGATGA AGGCGTCGCGGATGCGCCTCAAATTCAGTGCACAAACGTGCTGAAGATCCGCCGGCGGAAGATGA T G AURKAIP1 Ensembl:ENSG00000175756 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:1373778..1374175;chr1:1373778..1374465 32194978 MeRIP-seq:(Medium) rs781737581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323996,Human_RBP_ID_970538,Human_RBP_ID_5136575,Human_RBP_ID_10554281,Human_RBP_ID_18468411,Human_RBP_ID_22024523,Human_RBP_ID_22426812,Human_RBP_ID_23328308,Human_RBP_ID_26839822 66861 RMVar_ID_66861 Human_SNP_ID_302953 m1A Human chr1 - 1374706 1374706 1374706 ACTTCCCAGCTGTTGAGGGCCGTTCCTTGGGCAGGTAGGAAGCCGCGCGGGGGCGGATGGGAGGA ACTTCCCAGCTGTTGAGGGCCGTTCCTTGGGCTGGTAGGAAGCCGCGCGGGGGCGGATGGGAGGA T A AURKAIP1 Ensembl:ENSG00000175756 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1374701..1374857 26863410 MeRIP-seq:(Medium) rs1165509496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072408,Human_RBP_ID_5108370,Human_RBP_ID_17647258,Human_RBP_ID_22426026,Human_RBP_ID_22427975,Human_RBP_ID_26839832 Human_Splice_Rec_3739,Human_Splice_Rec_3744,Human_Splice_Rec_3745,Human_Splice_Rec_3750,Human_Splice_Rec_3751,Human_Splice_Rec_3756,Human_Splice_Rec_3757,Human_Splice_Rec_3762,Human_Splice_Rec_3763 66862 RMVar_ID_66862 Human_SNP_ID_303053 m1A Human chr1 + 1374961 1374956 1374962 CTTCCAACACAGCTCGCGCCCCGAGGCTCCCAAGCCCCCGACGCGGGCGGTGTCGCGCTCGGACG CTTCCAACACAGCTCGCGCCCCGAGGCT______CCCCCGACGCGGGCGGTGTCGCGCTCGGACG TCCCAAG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1374960..1375098 32194978 MeRIP-seq:(Medium) rs1002719732 Functional Loss DEL dbSNP153 29..34 33 - - - 66863 RMVar_ID_66863 Human_SNP_ID_303064 m1A Human chr1 - 1374981 1374981 1374981 CGTTCTGGGACCTTTCGGTGCGTCCGAGCGCGACACCGCCCGCGTCGGGGGCTTGGGAGCCTCGG CGTTCTGGGACCTTTCGGTGCGTCCGAGCGCGTCACCGCCCGCGTCGGGGGCTTGGGAGCCTCGG T A AURKAIP1 Ensembl:ENSG00000175756 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr1:1374976..1375200;chr1:1374976..1375175 26863196,26863410 MeRIP-seq:(Medium) rs1436778662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745623,Human_RBP_ID_5336538,Human_RBP_ID_9352450 66864 RMVar_ID_66864 Human_SNP_ID_305268 m1A Human chr1 - 1382294 1382294 1382294 GGGAAGGGTGGTGACCTCTGGATTGTTACTGGATTGTTGGGAAGGGGTGGTGGCCTCTGGATTGT GGGAAGGGTGGTGACCTCTGGATTGTTACTGGGTTGTTGGGAAGGGGTGGTGGCCTCTGGATTGT T C lnc-CCNL2-1-001 RNACentral:URS00008B4137 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1382232..1382675 26863196 MeRIP-seq:(Medium) rs958492955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10554447 66865 RMVar_ID_66865 Human_SNP_ID_307292 m1A Human chr1 - 1387985 1387985 1387985 TGAAGAACACCAAGAGGAGGCTGGAGGGCGCCAAGAAAGCCAAGGCGGACAGCCCCGTGAACGGG TGAAGAACACCAAGAGGAGGCTGGAGGGCGCCGAGAAAGCCAAGGCGGACAGCCCCGTGAACGGG T C CCNL2 Ensembl:ENSG00000221978 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1387854..1388089 32194978 MeRIP-seq:(Medium) rs750105467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744507,Human_RBP_ID_803994,Human_RBP_ID_853453,Human_RBP_ID_3932497,Human_RBP_ID_5518305,Human_RBP_ID_5536417,Human_RBP_ID_9355302,Human_RBP_ID_18468413,Human_RBP_ID_18964455,Human_RBP_ID_24540918,Human_RBP_ID_24579915,Human_RBP_ID_26309991,Human_RBP_ID_27797249 Human_Splice_Rec_3774,Human_Splice_Rec_3775,Human_Splice_Rec_3794,Human_Splice_Rec_3795,Human_Splice_Rec_3812,Human_Splice_Rec_3813,Human_Splice_Rec_3817,Human_Splice_Rec_3840,Human_Splice_Rec_3841,Human_Splice_Rec_3852,Human_Splice_Rec_3853,Human_Splice_Rec_3866,Human_Splice_Rec_3867,Human_Splice_Rec_3888,Human_Splice_Rec_3889,Human_Splice_Rec_3898,Human_Splice_Rec_3899,Human_Splice_Rec_3914,Human_Splice_Rec_3915,Human_Splice_Rec_3936,Human_Splice_Rec_3937,Human_Splice_Rec_3948,Human_Splice_Rec_3949,Human_Splice_Rec_3962 RMVar_hsa_circ_128324,RMVar_hsa_circ_376593 66866 RMVar_ID_66866 Human_SNP_ID_307293 m1A Human chr1 - 1387985 1387985 1387985 TGAAGAACACCAAGAGGAGGCTGGAGGGCGCCAAGAAAGCCAAGGCGGACAGCCCCGTGAACGGG TGAAGAACACCAAGAGGAGGCTGGAGGGCGCCCAGAAAGCCAAGGCGGACAGCCCCGTGAACGGG T G CCNL2 Ensembl:ENSG00000221978 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1387854..1388089 32194978 MeRIP-seq:(Medium) rs750105467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744507,Human_RBP_ID_803994,Human_RBP_ID_853453,Human_RBP_ID_3932497,Human_RBP_ID_5518305,Human_RBP_ID_5536417,Human_RBP_ID_9355302,Human_RBP_ID_18468413,Human_RBP_ID_18964455,Human_RBP_ID_24540918,Human_RBP_ID_24579915,Human_RBP_ID_26309991,Human_RBP_ID_27797249 Human_Splice_Rec_3774,Human_Splice_Rec_3775,Human_Splice_Rec_3794,Human_Splice_Rec_3795,Human_Splice_Rec_3812,Human_Splice_Rec_3813,Human_Splice_Rec_3817,Human_Splice_Rec_3840,Human_Splice_Rec_3841,Human_Splice_Rec_3852,Human_Splice_Rec_3853,Human_Splice_Rec_3866,Human_Splice_Rec_3867,Human_Splice_Rec_3888,Human_Splice_Rec_3889,Human_Splice_Rec_3898,Human_Splice_Rec_3899,Human_Splice_Rec_3914,Human_Splice_Rec_3915,Human_Splice_Rec_3936,Human_Splice_Rec_3937,Human_Splice_Rec_3948,Human_Splice_Rec_3949,Human_Splice_Rec_3962 RMVar_hsa_circ_128324,RMVar_hsa_circ_376593 66867 RMVar_ID_66867 Human_SNP_ID_307305 m1A Human chr1 - 1388009 1388009 1388009 GGAGCAAGCCTTCCCCACTGTCTGTGAAGAACACCAAGAGGAGGCTGGAGGGCGCCAAGAAAGCC GGAGCAAGCCTTCCCCACTGTCTGTGAAGAACCCCAAGAGGAGGCTGGAGGGCGCCAAGAAAGCC T G CCNL2 Ensembl:ENSG00000221978 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1387776..1388097 26863196 MeRIP-seq:(Medium) rs1217111066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23925,Human_RBP_ID_853453,Human_RBP_ID_3934881,Human_RBP_ID_5518305,Human_RBP_ID_9355302,Human_RBP_ID_10554579,Human_RBP_ID_18158180,Human_RBP_ID_18468413,Human_RBP_ID_18549734,Human_RBP_ID_18964455,Human_RBP_ID_22779495,Human_RBP_ID_22845811,Human_RBP_ID_24540918,Human_RBP_ID_26309991,Human_RBP_ID_27797249 Human_Splice_Rec_3774,Human_Splice_Rec_3775,Human_Splice_Rec_3794,Human_Splice_Rec_3795,Human_Splice_Rec_3812,Human_Splice_Rec_3813,Human_Splice_Rec_3817,Human_Splice_Rec_3840,Human_Splice_Rec_3841,Human_Splice_Rec_3852,Human_Splice_Rec_3853,Human_Splice_Rec_3866,Human_Splice_Rec_3867,Human_Splice_Rec_3888,Human_Splice_Rec_3889,Human_Splice_Rec_3898,Human_Splice_Rec_3899,Human_Splice_Rec_3914,Human_Splice_Rec_3915,Human_Splice_Rec_3936,Human_Splice_Rec_3937,Human_Splice_Rec_3948,Human_Splice_Rec_3949,Human_Splice_Rec_3962 Human_miRNA_ID_2971969,Human_miRNA_ID_3005154 RMVar_hsa_circ_128324,RMVar_hsa_circ_376593 66868 RMVar_ID_66868 Human_SNP_ID_311258 m1A Human chr1 - 1399223 1399223 1399223 GCAGCGGCCGGCGCCCCGGGATCTGGGGGCGCACCCTCAGGGTCGCAGGGGGTGCTGATCGGGGA GCAGCGGCCGGCGCCCCGGGATCTGGGGGCGCGCCCTCAGGGTCGCAGGGGGTGCTGATCGGGGA T C CCNL2 Ensembl:ENSG00000221978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1399176..1399350 26863196 MeRIP-seq:(Medium) rs914312123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3279304,Human_RBP_ID_17723779,Human_RBP_ID_18414817,Human_RBP_ID_18964475,Human_RBP_ID_22025798,Human_RBP_ID_22561978,Human_RBP_ID_26315732,Human_RBP_ID_26753144,Human_RBP_ID_27797255 66869 RMVar_ID_66869 Human_SNP_ID_311280 m1A Human chr1 - 1399253 1399253 1399253 GCTGGTGCTGCAGGGTCGGCAGCTCCCGCGGCAGCGGCCGGCGCCCCGGGATCTGGGGGCGCACC GCTGGTGCTGCAGGGTCGGCAGCTCCCGCGGCGGCGGCCGGCGCCCCGGGATCTGGGGGCGCACC T C CCNL2 Ensembl:ENSG00000221978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1399151..1399325 26863410 MeRIP-seq:(Medium) rs1285294006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073416,Human_RBP_ID_18414817,Human_RBP_ID_26753144 66870 RMVar_ID_66870 Human_SNP_ID_311287 m1A Human chr1 + 1399262 1399262 1399262 CCAGATCCCGGGGCGCCGGCCGCTGCCGCGGGAGCTGCCGACCCTGCAGCACCAGCCGCCGCCGC CCAGATCCCGGGGCGCCGGCCGCTGCCGCGGGGGCTGCCGACCCTGCAGCACCAGCCGCCGCCGC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr1:1399218..1399315;chr1:1399197..1399310 26863410 MeRIP-seq:(Medium) rs767674235 Functional Loss SNV dbSNP153 33..33 33 - - - 66871 RMVar_ID_66871 Human_SNP_ID_311305 m1A Human chr1 + 1399280 1399280 1399280 GCCGCTGCCGCGGGAGCTGCCGACCCTGCAGCACCAGCCGCCGCCGCCGCCGCCGCCATTTTGTG GCCGCTGCCGCGGGAGCTGCCGACCCTGCAGCCCCAGCCGCCGCCGCCGCCGCCGCCATTTTGTG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:1399201..1399312 26863410 MeRIP-seq:(Medium) rs998788746 Functional Loss SNV dbSNP153 33..33 33 - - - 66872 RMVar_ID_66872 Human_SNP_ID_311533 m1A Human chr1 - 1399619 1399619 1399619 CTGTGCGAACGTGGGCATCTTGGAAGAGTCCCAGCCCCGCTCGGGGCGCACAGGCAGGCGCTCTC CTGTGCGAACGTGGGCATCTTGGAAGAGTCCCTGCCCCGCTCGGGGCGCACAGGCAGGCGCTCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1399583..1399675 26863196 MeRIP-seq:(Medium) rs1050382088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18549833 66873 RMVar_ID_66873 Human_SNP_ID_311534 m1A Human chr1 - 1399619 1399619 1399619 CTGTGCGAACGTGGGCATCTTGGAAGAGTCCCAGCCCCGCTCGGGGCGCACAGGCAGGCGCTCTC CTGTGCGAACGTGGGCATCTTGGAAGAGTCCCGGCCCCGCTCGGGGCGCACAGGCAGGCGCTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1399583..1399675 26863196 MeRIP-seq:(Medium) rs1050382088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18549833 66874 RMVar_ID_66874 Human_SNP_ID_311699 m1A Human chr1 - 1400002 1399987 1400003 CTCCTTCCGTGGGCCTGAACCTTGAGGTACTTAGGCCTCCCCACGCTGGAGGGGCTCTGTAGGGA CTCCTTCCGTGGGCCTGAACCTTGAGGTACT________________GGAGGGGCTCTGTAGGGA CAGCGTGGGGAGGCCTA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1399996..1400161 26863196 MeRIP-seq:(Medium) rs1417427871 Functional Loss DEL dbSNP153 32..47 33 - - - 66875 RMVar_ID_66875 Human_SNP_ID_312520 m1A Human chr1 + 1402076 1402075 1402077 TTACTCTGTCTCTTTTCCTAATCAATACAGCAACAGTCCTCAGTGGTACTGCACCACTCTGGAAA TTACTCTGTCTCTTTTCCTAATCAATACAGCA__AGTCCTCAGTGGTACTGCACCACTCTGGAAA AAC A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:1402026..1402256 32194978 MeRIP-seq:(Medium) rs759673310 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2090945,Human_RBP_ID_3279313 66876 RMVar_ID_66876 Human_SNP_ID_312521 m1A Human chr1 + 1402076 1402076 1402076 TTACTCTGTCTCTTTTCCTAATCAATACAGCAACAGTCCTCAGTGGTACTGCACCACTCTGGAAA TTACTCTGTCTCTTTTCCTAATCAATACAGCAGCAGTCCTCAGTGGTACTGCACCACTCTGGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:1402026..1402256 32194978 MeRIP-seq:(Medium) rs1200517370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2090945,Human_RBP_ID_3279313 66877 RMVar_ID_66877 Human_SNP_ID_312565 m1A Human chr1 - 1402155 1402154 1402155 TTGGCTGCCTTGGCCAGTAGGAGGCGACACGAAGGATTTGCTGCTGCCTTGGGGGATGGGAAGGA TTGGCTGCCTTGGCCAGTAGGAGGCGACACGA_GGATTTGCTGCTGCCTTGGGGGATGGGAAGGA CT C MRPL20 Ensembl:ENSG00000242485 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1402104..1402200 26863196 MeRIP-seq:(Medium) rs1437939447 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_324124,Human_RBP_ID_1410305,Human_RBP_ID_5681698,Human_RBP_ID_10555041,Human_RBP_ID_18549850,Human_RBP_ID_27166795 66878 RMVar_ID_66878 Human_SNP_ID_312566 m1A Human chr1 - 1402155 1402155 1402155 TTGGCTGCCTTGGCCAGTAGGAGGCGACACGAAGGATTTGCTGCTGCCTTGGGGGATGGGAAGGA TTGGCTGCCTTGGCCAGTAGGAGGCGACACGATGGATTTGCTGCTGCCTTGGGGGATGGGAAGGA T A MRPL20 Ensembl:ENSG00000242485 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1402104..1402200 26863196 MeRIP-seq:(Medium) rs1184544105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324124,Human_RBP_ID_1410305,Human_RBP_ID_5681698,Human_RBP_ID_10555041,Human_RBP_ID_18549850,Human_RBP_ID_27166795 66879 RMVar_ID_66879 Human_SNP_ID_314219 m1A Human chr1 - 1406568 1406568 1406568 CTTCCCTTCCCTTTGGCAGCTGAAGTCAACCCAGCCCCTTGCCAACCCTCCAGGGCTACTATCTG CTTCCCTTCCCTTTGGCAGCTGAAGTCAACCCGGCCCCTTGCCAACCCTCCAGGGCTACTATCTG T C MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1406566..1406779 26863196 MeRIP-seq:(Medium) rs1173171407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1410329,Human_RBP_ID_17070938,Human_RBP_ID_22022575 66880 RMVar_ID_66880 Human_SNP_ID_314230 m1A Human chr1 + 1406598 1406598 1406598 GCTGGGTTGACTTCAGCTGCCAAAGGGAAGGGAAGCCACCGGAGGGATGAGAGCAGCAGCGACTA GCTGGGTTGACTTCAGCTGCCAAAGGGAAGGGCAGCCACCGGAGGGATGAGAGCAGCAGCGACTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1406595..1406719 26863196 MeRIP-seq:(Medium) rs1557751638 Functional Loss SNV dbSNP153 33..33 33 - - - 66881 RMVar_ID_66881 Human_SNP_ID_314523 m1A Human chr1 - 1407153 1407153 1407153 GAATCGCGTCACCGACCGCTACTTTCGGATCCAGGAGGTGCTGAAGCACGCCAGGGTGAGTGCCG GAATCGCGTCACCGACCGCTACTTTCGGATCCTGGAGGTGCTGAAGCACGCCAGGGTGAGTGCCG T A MRPL20 Ensembl:ENSG00000242485 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1407151..1407300 26863196 MeRIP-seq:(Medium) rs556155223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103546,Human_RBP_ID_1410332,Human_RBP_ID_4072414,Human_RBP_ID_8734031,Human_RBP_ID_23117598 Human_Splice_Rec_4023,Human_Splice_Rec_4033,Human_Splice_Rec_4041,Human_Splice_Rec_4045 Human_miRNA_ID_207546 66882 RMVar_ID_66882 Human_SNP_ID_314524 m1A Human chr1 - 1407153 1407153 1407153 GAATCGCGTCACCGACCGCTACTTTCGGATCCAGGAGGTGCTGAAGCACGCCAGGGTGAGTGCCG GAATCGCGTCACCGACCGCTACTTTCGGATCCCGGAGGTGCTGAAGCACGCCAGGGTGAGTGCCG T G MRPL20 Ensembl:ENSG00000242485 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1407151..1407300 26863196 MeRIP-seq:(Medium) rs556155223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103546,Human_RBP_ID_1410332,Human_RBP_ID_4072414,Human_RBP_ID_8734031,Human_RBP_ID_23117598 Human_Splice_Rec_4023,Human_Splice_Rec_4033,Human_Splice_Rec_4041,Human_Splice_Rec_4045 Human_miRNA_ID_207546 66883 RMVar_ID_66883 Human_SNP_ID_314576 m1A Human chr1 + 1407227 1407227 1407227 AGCTGCGCGGTGAGGAAGACCATGGCGCCTGCAGGCCGGCGTCCCGAACACTCAACAACGCACGC AGCTGCGCGGTGAGGAAGACCATGGCGCCTGCTGGCCGGCGTCCCGAACACTCAACAACGCACGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1407176..1407300 26863196 MeRIP-seq:(Medium) rs1220732053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18549863 66884 RMVar_ID_66884 Human_SNP_ID_314700 m1A Human chr1 + 1407449 1407421 1407450 GATGTGGGGCCGCGGCGGGGACTGAAAGGAGAACGGGGCCGCAGCGCCCGTGGCTATTCGCGGAC GATGT_____________________________GGGGCCGCAGCGCCCGTGGCTATTCGCGGAC TGGGGCCGCGGCGGGGACTGAAAGGAGAAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:1407399..1407677;chr1:1407401..1407676 26863196 MeRIP-seq:(Medium) rs1200485411 Functional Loss DEL dbSNP153 6..34 33 - - - Human_RBP_ID_10555261 66885 RMVar_ID_66885 Human_SNP_ID_314918 m1A Human chr1 + 1407964 1407964 1407964 TACAGGCCTGAGCCACCGCGCCATGCCTGGAAATTCTCAGCTTCGAAATGGTAAATGTGATCGCT TACAGGCCTGAGCCACCGCGCCATGCCTGGAAGTTCTCAGCTTCGAAATGGTAAATGTGATCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1407927..1408012 26863196 MeRIP-seq:(Medium) rs1403392020 Functional Loss SNV dbSNP153 33..33 33 - - - 66886 RMVar_ID_66886 Human_SNP_ID_325545 m1A Human chr1 + 1437299 1437299 1437299 GCTGGTGTGGGTGACAGATGGCGGCTCCAGCGACCCTGTGGGCCCCCCCATGCAGGAGCTCAAGG GCTGGTGTGGGTGACAGATGGCGGCTCCAGCGGCCCTGTGGGCCCCCCCATGCAGGAGCTCAAGG A G VWA1 Ensembl:ENSG00000179403 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1437015..1439556 32194978 MeRIP-seq:(Medium) rs769025589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324148,Human_RBP_ID_5137311,Human_RBP_ID_22427983,Human_RBP_ID_22750624,Human_RBP_ID_24550430 66887 RMVar_ID_66887 Human_SNP_ID_326532 m1A Human chr1 + 1439804 1439804 1439804 CAGCCGTGAGCCGTAAGCCGGCGTCCCCGCCCAGCCGAGAGGGCCGGCGCCTACCTGAGGGCCCC CAGCCGTGAGCCGTAAGCCGGCGTCCCCGCCCGGCCGAGAGGGCCGGCGCCTACCTGAGGGCCCC A G VWA1 Ensembl:ENSG00000179403 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1439707..1440052 26863410 MeRIP-seq:(Medium) rs1432658750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17647264,Human_RBP_ID_22428955 66888 RMVar_ID_66888 Human_SNP_ID_337726 m1A Human chr1 - 1471450 1471450 1471450 GCGCTCGCGGCGGCCCCGACTCTCTCCTTGATAGGAATGGTTGACTTCACAGAATTATATGGAGT GCGCTCGCGGCGGCCCCGACTCTCTCCTTGATGGGAATGGTTGACTTCACAGAATTATATGGAGT T C lnc-TMEM240-2,lnc-TMEM240-2:2 RNACentral:URS0000D579C3,RNACentral:URS0000D5CEEB lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1471444..1471570 26863196 MeRIP-seq:(Medium) rs1312388736 Functional Loss SNV dbSNP153 33..33 33 - - - 66889 RMVar_ID_66889 Human_SNP_ID_337729 m1A Human chr1 + 1471460 1471456 1471460 ATTCTGTGAAGTCAACCATTCCTATCAAGGAGAGAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG ATTCTGTGAAGTCAACCATTCCTATCAAG____GAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG GGAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471432..1471624 26863196 MeRIP-seq:(Medium) rs1353593729 Functional Loss DEL dbSNP153 30..33 33 - - - 66890 RMVar_ID_66890 Human_SNP_ID_337730 m1A Human chr1 + 1471460 1471456 1471460 ATTCTGTGAAGTCAACCATTCCTATCAAGGAGAGAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG ATTCTGTGAAGTCAACCATTCCTATCAAGGA__GAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG GGAGA GGA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471432..1471624 26863196 MeRIP-seq:(Medium) rs1353593729 Functional Loss DEL dbSNP153 32..33 33 - - - 66891 RMVar_ID_66891 Human_SNP_ID_337731 m1A Human chr1 + 1471460 1471460 1471460 ATTCTGTGAAGTCAACCATTCCTATCAAGGAGAGAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG ATTCTGTGAAGTCAACCATTCCTATCAAGGAGGGAGTCGGGGCCGCCGCGAGCGCGTGAACCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471432..1471624 26863196 MeRIP-seq:(Medium) rs867043539 Functional Loss SNV dbSNP153 33..33 33 - - - 66892 RMVar_ID_66892 Human_SNP_ID_337912 m1A Human chr1 - 1471814 1471814 1471814 CACCCGAGTCTGACTCGGGCGCGGCTGGGAGCAGCCTCCACGCGCCGCGAGCCGGTGGCCAGGAC CACCCGAGTCTGACTCGGGCGCGGCTGGGAGCTGCCTCCACGCGCCGCGAGCCGGTGGCCAGGAC T A lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1471776..1472050 26863196 MeRIP-seq:(Medium) rs1372314280 Functional Loss SNV dbSNP153 33..33 33 - - - 66893 RMVar_ID_66893 Human_SNP_ID_337918 m1A Human chr1 + 1471821 1471821 1471821 CCACCGGCTCGCGGCGCGTGGAGGCTGCTCCCAGCCGCGCCCGAGTCAGACTCGGGTGGGGGTCC CCACCGGCTCGCGGCGCGTGGAGGCTGCTCCCCGCCGCGCCCGAGTCAGACTCGGGTGGGGGTCC A C ATAD3B Ensembl:ENSG00000160072 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1471812..1472025 26863196 MeRIP-seq:(Medium) rs1188532592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074977,Human_RBP_ID_9318426,Human_RBP_ID_18415911 RMVar_hsa_circ_92996,RMVar_hsa_circ_128329 66894 RMVar_ID_66894 Human_SNP_ID_338004 m1A Human chr1 - 1471992 1471992 1471992 CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAAACCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAAGCCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471794..1472050 26863196 MeRIP-seq:(Medium) rs188574574 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 66895 RMVar_ID_66895 Human_SNP_ID_338005 m1A Human chr1 - 1471992 1471992 1471992 CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAAACCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAACCCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG T G lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471794..1472050 26863196 MeRIP-seq:(Medium) rs188574574 Functional Loss SNV dbSNP153 33..33 33 - - - 66896 RMVar_ID_66896 Human_SNP_ID_340022 m1A Human chr1 + 1477373 1477373 1477373 CAAGCTCAAAGTGAGTGGGGCCGGTGTGGGCGAGGAGGCCGGGGCGCACATGGGGTTCAGGCGTG CAAGCTCAAAGTGAGTGGGGCCGGTGTGGGCGGGGAGGCCGGGGCGCACATGGGGTTCAGGCGTG A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1477371..1477483 26863196 MeRIP-seq:(Medium) rs1240840716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5336551,Human_RBP_ID_8166159,Human_RBP_ID_10556162,Human_RBP_ID_18927757,Human_RBP_ID_19033590,Human_RBP_ID_22557496,Human_RBP_ID_27835038 Human_Splice_Rec_4126,Human_Splice_Rec_4156 RMVar_hsa_circ_92996,RMVar_hsa_circ_128329 66897 RMVar_ID_66897 Human_SNP_ID_340536 m1A Human chr1 + 1478565 1478565 1478565 CTAGTCTGGGCACGGAGTCTCTGCCGTGCCGGAGCTGTGCAGACACAGGAGCGGCTGTCAGGCAG CTAGTCTGGGCACGGAGTCTCTGCCGTGCCGGCGCTGTGCAGACACAGGAGCGGCTGTCAGGCAG A C ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1478375..1478576 32194978 MeRIP-seq:(Medium) rs529874726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1344529,Human_RBP_ID_10556242,Human_RBP_ID_22022582,Human_RBP_ID_22413846 RMVar_hsa_circ_103406,RMVar_hsa_circ_94982,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_114161,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128330,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_128332,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128338,RMVar_hsa_circ_95397,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_128333 66898 RMVar_ID_66898 Human_SNP_ID_342171 m1A Human chr1 + 1482194 1482194 1482194 TGCGGCACAAGAATGAGATGCTGCGAGTGGAGACCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG TGCGGCACAAGAATGAGATGCTGCGAGTGGAGCCCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG A C ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1482141..1482295 26863196 MeRIP-seq:(Medium) rs747464654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804487,Human_RBP_ID_3932508,Human_RBP_ID_9355314,Human_RBP_ID_10556369,Human_RBP_ID_18966828,Human_RBP_ID_22871683,Human_RBP_ID_26309997,Human_RBP_ID_27797257 Human_Splice_Rec_4134,Human_Splice_Rec_4186,Human_Splice_Rec_4210 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 66899 RMVar_ID_66899 Human_SNP_ID_342172 m1A Human chr1 + 1482194 1482194 1482194 TGCGGCACAAGAATGAGATGCTGCGAGTGGAGACCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG TGCGGCACAAGAATGAGATGCTGCGAGTGGAGGCCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG A G ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1482141..1482295 26863196 MeRIP-seq:(Medium) rs747464654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804487,Human_RBP_ID_3932508,Human_RBP_ID_9355314,Human_RBP_ID_10556369,Human_RBP_ID_18966828,Human_RBP_ID_22871683,Human_RBP_ID_26309997,Human_RBP_ID_27797257 Human_Splice_Rec_4134,Human_Splice_Rec_4186,Human_Splice_Rec_4210 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 66900 RMVar_ID_66900 Human_SNP_ID_342173 m1A Human chr1 + 1482194 1482194 1482194 TGCGGCACAAGAATGAGATGCTGCGAGTGGAGACCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG TGCGGCACAAGAATGAGATGCTGCGAGTGGAGTCCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG A T ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1482141..1482295 26863196 MeRIP-seq:(Medium) rs747464654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804487,Human_RBP_ID_3932508,Human_RBP_ID_9355314,Human_RBP_ID_10556369,Human_RBP_ID_18966828,Human_RBP_ID_22871683,Human_RBP_ID_26309997,Human_RBP_ID_27797257 Human_Splice_Rec_4134,Human_Splice_Rec_4186,Human_Splice_Rec_4210 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 66901 RMVar_ID_66901 Human_SNP_ID_342214 m1A Human chr1 + 1482237 1482237 1482237 GGCGCGCGCCAAGGCCGAGCGGGAGAATGCAGACATCATCCGCGAGCAGATCCGCCTGAAGGCGT GGCGCGCGCCAAGGCCGAGCGGGAGAATGCAGGCATCATCCGCGAGCAGATCCGCCTGAAGGCGT A G ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1482186..1482287 32194978 MeRIP-seq:(Medium) rs759198461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934893,Human_RBP_ID_9355314,Human_RBP_ID_26309998 Human_Splice_Rec_4134,Human_Splice_Rec_4135,Human_Splice_Rec_4161,Human_Splice_Rec_4186,Human_Splice_Rec_4187,Human_Splice_Rec_4210,Human_Splice_Rec_4211 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 66902 RMVar_ID_66902 Human_SNP_ID_342241 m1A Human chr1 + 1482282 1482282 1482282 GCAGATCCGCCTGAAGGCGTCCGAGCACCGTCAGACCGTCTTGGAGTCCATCAGGTGAGCACTGC GCAGATCCGCCTGAAGGCGTCCGAGCACCGTCGGACCGTCTTGGAGTCCATCAGGTGAGCACTGC A G ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1482186..1482300 26863410 MeRIP-seq:(Medium) rs143114169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804636,Human_RBP_ID_853467,Human_RBP_ID_3934893,Human_RBP_ID_9355315,Human_RBP_ID_18966829,Human_RBP_ID_26309998 Human_Splice_Rec_4135,Human_Splice_Rec_4160,Human_Splice_Rec_4161,Human_Splice_Rec_4187,Human_Splice_Rec_4211 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 66903 RMVar_ID_66903 Human_SNP_ID_342577 m1A Human chr1 + 1482951 1482951 1482951 TAAGCCCAGGAGGTTTGGGCTGCAGTGAGCCAACATTGCACCACTGCACTCCATTCTTGGCGAGA TAAGCCCAGGAGGTTTGGGCTGCAGTGAGCCAGCATTGCACCACTGCACTCCATTCTTGGCGAGA A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1482946..1483035 26863196 MeRIP-seq:(Medium) rs1036440453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5332510,Human_RBP_ID_8283617,Human_RBP_ID_10556377,Human_RBP_ID_22845950,Human_RBP_ID_24580504 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_109226,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341,RMVar_hsa_circ_36428 66904 RMVar_ID_66904 Human_SNP_ID_344973 m1A Human chr1 - 1487895 1487895 1487895 TAGTGACACTCACAGTGGCTCGCTTCCGAAGGAAGGCGTCTGCTTCATCCATGAAGAGCAGGAGG TAGTGACACTCACAGTGGCTCGCTTCCGAAGGCAGGCGTCTGCTTCATCCATGAAGAGCAGGAGG T G lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1486611..1487906 26863410 MeRIP-seq:(Medium) rs751189348 Functional Loss SNV dbSNP153 33..33 33 - - - 66905 RMVar_ID_66905 Human_SNP_ID_347969 m1A Human chr1 + 1495480 1495480 1495480 CATAGCGGCCTCCCTCAGCTCCCTCTCTCTTCACTAGGCCACGGCATATGCCTCCAAGGACGGGG CATAGCGGCCTCCCTCAGCTCCCTCTCTCTTCGCTAGGCCACGGCATATGCCTCCAAGGACGGGG A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1495478..1495585 26863196 MeRIP-seq:(Medium) rs1312448719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22632679,Human_RBP_ID_22735291 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_109226,RMVar_hsa_circ_128333,RMVar_hsa_circ_99389,RMVar_hsa_circ_128342,RMVar_hsa_circ_128343,RMVar_hsa_circ_104837,RMVar_hsa_circ_128344,RMVar_hsa_circ_128346 66906 RMVar_ID_66906 Human_SNP_ID_348306 m1A Human chr1 - 1495915 1495915 1495915 ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTACAAAGCCTCACCCTCCCCCTGTGAGCCAGACG ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTTCAAAGCCTCACCCTCCCCCTGTGAGCCAGACG T A lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1495908..1496027 26863196 MeRIP-seq:(Medium) rs1030185265 Functional Loss SNV dbSNP153 33..33 33 - - - 66907 RMVar_ID_66907 Human_SNP_ID_348307 m1A Human chr1 - 1495915 1495915 1495915 ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTACAAAGCCTCACCCTCCCCCTGTGAGCCAGACG ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTGCAAAGCCTCACCCTCCCCCTGTGAGCCAGACG T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1495908..1496027 26863196 MeRIP-seq:(Medium) rs1030185265 Functional Loss SNV dbSNP153 33..33 33 - - - 66908 RMVar_ID_66908 Human_SNP_ID_354235 m1A Human chr1 - 1511512 1511512 1511512 CCGGGCAGGCGCCGCCCCGGAGCCCACGGTCCACGCGCTCCCAGCGGCCCTGACTTTCTCCTTGA CCGGGCAGGCGCCGCCCCGGAGCCCACGGTCCGCGCGCTCCCAGCGGCCCTGACTTTCTCCTTGA T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1511505..1511880 26863196 MeRIP-seq:(Medium) rs1323707392 Functional Loss SNV dbSNP153 33..33 33 - - - 66909 RMVar_ID_66909 Human_SNP_ID_354523 m1A Human chr1 - 1512201 1512201 1512201 CCCCACCCGAGTCTGACTCGCGCGCGGCTGGGAGCAGCCTCCACGCGCCGCGAGCCGGTGGTCAC CCCCACCCGAGTCTGACTCGCGCGCGGCTGGGTGCAGCCTCCACGCGCCGCGAGCCGGTGGTCAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512126..1512475 26863196 MeRIP-seq:(Medium) rs1002388048 Functional Loss SNV dbSNP153 33..33 33 - - - 66910 RMVar_ID_66910 Human_SNP_ID_354535 m1A Human chr1 + 1512216 1512216 1512216 CGGCGCGTGGAGGCTGCTCCCAGCCGCGCGCGAGTCAGACTCGGGTGGGGGTCCCGGCGGCGGTA CGGCGCGTGGAGGCTGCTCCCAGCCGCGCGCGTGTCAGACTCGGGTGGGGGTCCCGGCGGCGGTA A T ATAD3A Ensembl:ENSG00000197785 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr1:1512166..1512308;chr1:1512176..1512351 26863196 MeRIP-seq:(Medium) rs962726816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072426 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66911 RMVar_ID_66911 Human_SNP_ID_354571 m1A Human chr1 - 1512262 1512262 1512262 TTGTTAATGCCGAAGAGCCACGACATGCTCGCACCGCCGCCGCCGCTACCGCCGCCGGGACCCCC TTGTTAATGCCGAAGAGCCACGACATGCTCGCCCCGCCGCCGCCGCTACCGCCGCCGGGACCCCC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:1512176..1512299 26863410 MeRIP-seq:(Medium) rs1332255926 Functional Loss SNV dbSNP153 33..33 33 - - - 66912 RMVar_ID_66912 Human_SNP_ID_354573 m1A Human chr1 + 1512266 1512266 1512266 GTCCCGGCGGCGGTAGCGGCGGCGGCGGTGCGAGCATGTCGTGGCTCTTCGGCATTAACAAGGGC GTCCCGGCGGCGGTAGCGGCGGCGGCGGTGCGGGCATGTCGTGGCTCTTCGGCATTAACAAGGGC A G ATAD3A Ensembl:ENSG00000197785 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:1512176..1512400 26863410 MeRIP-seq:(Medium) rs1434372930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5108378,Human_RBP_ID_17762278 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66913 RMVar_ID_66913 Human_SNP_ID_354583 m1A Human chr1 + 1512293 1512293 1512293 GTGCGAGCATGTCGTGGCTCTTCGGCATTAACAAGGGCCCCAAGGGTGAAGGCGCGGGGCCGCCG GTGCGAGCATGTCGTGGCTCTTCGGCATTAACGAGGGCCCCAAGGGTGAAGGCGCGGGGCCGCCG A G ATAD3A Ensembl:ENSG00000197785 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1512199..1512336 26863410 MeRIP-seq:(Medium) rs911686477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_970572,Human_RBP_ID_17762278 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66914 RMVar_ID_66914 Human_SNP_ID_354664 m1A Human chr1 + 1512515 1512488 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGG___________________________CGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGCGCGGGCGGGCGGGCGGGA G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs774187948 Functional Loss DEL dbSNP153 7..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66915 RMVar_ID_66915 Human_SNP_ID_354676 m1A Human chr1 + 1512515 1512493 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGGG______________________CGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGCGCGGGCGGGCGGGCGGGA G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs771625189 Functional Loss DEL dbSNP153 12..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66916 RMVar_ID_66916 Human_SNP_ID_354691 m1A Human chr1 + 1512515 1512498 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGGGCGGCG_________________CGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGCGGGCGGGCGGGA G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs1009000738 Functional Loss DEL dbSNP153 17..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66917 RMVar_ID_66917 Human_SNP_ID_354694 m1A Human chr1 + 1512515 1512501 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGGGCGGCGCGG______________CGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GGCGGGCGGGCGGGA G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs766030533 Functional Loss DEL dbSNP153 20..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66918 RMVar_ID_66918 Human_SNP_ID_354705 m1A Human chr1 + 1512515 1512515 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGCCGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC A C ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs1192611150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66919 RMVar_ID_66919 Human_SNP_ID_354706 m1A Human chr1 + 1512515 1512515 1512515 GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGACGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC GCGGGGCGGGGCGGCGCGGGCGGGCGGGCGGGGCGGGCCGGGGAAGCGGGAGCCCTGGCCCTTGC A G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1512492..1512606 26863196 MeRIP-seq:(Medium) rs1192611150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_128347 66920 RMVar_ID_66920 Human_SNP_ID_356185 m1A Human chr1 - 1517174 1517174 1517174 AGACTAGTGTGTGCAGCAGGCTCAGGGCTTCCAGCCGCATCTGCACCCAGGATCAGGCCCTGGAG AGACTAGTGTGTGCAGCAGGCTCAGGGCTTCCGGCCGCATCTGCACCCAGGATCAGGCCCTGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1517168..1517267 26863196 MeRIP-seq:(Medium) rs1461394493 Functional Loss SNV dbSNP153 33..33 33 - - - 66921 RMVar_ID_66921 Human_SNP_ID_358709 m1A Human chr1 + 1522699 1522699 1522699 GGCAGCCCCGTGCGTCTCCTGCTCTAAGAGGGAGGGACGGTGGGGGCCGGTGCGCCAGTGCGGTG GGCAGCCCCGTGCGTCTCCTGCTCTAAGAGGGTGGGACGGTGGGGGCCGGTGCGCCAGTGCGGTG A T ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1522697..1522826 26863196 MeRIP-seq:(Medium) rs1432069158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22534717 RMVar_hsa_circ_89217,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_128344,RMVar_hsa_circ_64308,RMVar_hsa_circ_128347,RMVar_hsa_circ_372400,RMVar_hsa_circ_128349,RMVar_hsa_circ_105220,RMVar_hsa_circ_41103,RMVar_hsa_circ_128350 66922 RMVar_ID_66922 Human_SNP_ID_361302 m1A Human chr1 - 1528775 1528775 1528775 CCGGAAAGCTGGGCTGGCATGGAGCAGGCGGCAGCGGCAACCAGGCTCTCTTTTGTCATCACTGG CCGGAAAGCTGGGCTGGCATGGAGCAGGCGGCTGCGGCAACCAGGCTCTCTTTTGTCATCACTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1528773..1528844 26863196 MeRIP-seq:(Medium) rs1395274329 Functional Loss SNV dbSNP153 33..33 33 - - - 66923 RMVar_ID_66923 Human_SNP_ID_363208 m1A Human chr1 - 1533991 1533990 1533992 CAGCACATCTTCTGCTGGTGCTGCTGGACAGCATCTTGCACGCGGGTGTCCATCATGGCCTCGGT CAGCACATCTTCTGCTGGTGCTGCTGGACAG__TCTTGCACGCGGGTGTCCATCATGGCCTCGGT ATG A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1529300..1533994 26863410 MeRIP-seq:(Medium) rs770712866 Functional Loss DEL dbSNP153 32..33 33 - - - 66924 RMVar_ID_66924 Human_SNP_ID_363209 m1A Human chr1 - 1533991 1533991 1533991 CAGCACATCTTCTGCTGGTGCTGCTGGACAGCATCTTGCACGCGGGTGTCCATCATGGCCTCGGT CAGCACATCTTCTGCTGGTGCTGCTGGACAGCGTCTTGCACGCGGGTGTCCATCATGGCCTCGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1529300..1533994 26863410 MeRIP-seq:(Medium) rs983375046 Functional Loss SNV dbSNP153 33..33 33 - - - 66925 RMVar_ID_66925 Human_SNP_ID_363234 m1A Human chr1 - 1534019 1534019 1534019 CCCACGCCCAGGCCCTTCCGCCTTCAGCCAGCACATCTTCTGCTGGTGCTGCTGGACAGCATCTT CCCACGCCCAGGCCCTTCCGCCTTCAGCCAGCGCATCTTCTGCTGGTGCTGCTGGACAGCATCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1533981..1534124 26863196 MeRIP-seq:(Medium) rs41285842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1249970 66926 RMVar_ID_66926 Human_SNP_ID_363299 m1A Human chr1 + 1534091 1534091 1534091 CCTCCCCATCCTGAGTCCACAGGGAGATCCACAGCTCACGGAGCCTGGCCGCGGACCCCTCCCAC CCTCCCCATCCTGAGTCCACAGGGAGATCCACGGCTCACGGAGCCTGGCCGCGGACCCCTCCCAC A G ATAD3A Ensembl:ENSG00000197785 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1533999..1534125 26863196 MeRIP-seq:(Medium) rs1260875591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103227,Human_RBP_ID_324871,Human_RBP_ID_8284113,Human_RBP_ID_9319606,Human_RBP_ID_18186733,Human_RBP_ID_22426813,Human_RBP_ID_26367572 66927 RMVar_ID_66927 Human_SNP_ID_363514 m1A Human chr1 - 1534439 1534439 1534439 CCTCACCTGGCTCTGCTGTGGGAGCCGAGAACAAAGACATCACCTGCCTGGCTCCTGCTGCCCCG CCTCACCTGGCTCTGCTGTGGGAGCCGAGAACGAAGACATCACCTGCCTGGCTCCTGCTGCCCCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1534389..1534588 32194978 MeRIP-seq:(Medium) rs1261616026 Functional Loss SNV dbSNP153 33..33 33 - - - 66928 RMVar_ID_66928 Human_SNP_ID_363517 m1A Human chr1 - 1534449 1534449 1534449 GCAGGCGCCCCCTCACCTGGCTCTGCTGTGGGAGCCGAGAACAAAGACATCACCTGCCTGGCTCC GCAGGCGCCCCCTCACCTGGCTCTGCTGTGGGGGCCGAGAACAAAGACATCACCTGCCTGGCTCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1534340..1534489 26863410 MeRIP-seq:(Medium) rs1382711580 Functional Loss SNV dbSNP153 33..33 33 - - - 66929 RMVar_ID_66929 Human_SNP_ID_363555 m1A Human chr1 + 1534550 1534548 1534550 TTCCCCCTGTGGCCGGCATGCCCCGATCTTTCACACACTGGTGACCCTGAGAGAGGAGGGAGGAG TTCCCCCTGTGGCCGGCATGCCCCGATCTTT__CACACTGGTGACCCTGAGAGAGGAGGGAGGAG TCA T ATAD3A Ensembl:ENSG00000197785 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1534346..1534625 26863196 MeRIP-seq:(Medium) rs1049392901 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26385029,Human_RBP_ID_27387385 66930 RMVar_ID_66930 Human_SNP_ID_363558 m1A Human chr1 + 1534561 1534561 1534561 GCCGGCATGCCCCGATCTTTCACACACTGGTGACCCTGAGAGAGGAGGGAGGAGGGAACCTGGCG GCCGGCATGCCCCGATCTTTCACACACTGGTGTCCCTGAGAGAGGAGGGAGGAGGGAACCTGGCG A T ATAD3A Ensembl:ENSG00000197785 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1534512..1534609 26863196 MeRIP-seq:(Medium) rs1207394833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3990524,Human_RBP_ID_5136029,Human_RBP_ID_18157679,Human_RBP_ID_26367578 66931 RMVar_ID_66931 Human_SNP_ID_366013 m1A Human chr1 - 1540579 1540579 1540579 CCGAGCGCATCGCAGGGAGGACCCGAGGGCGGAGCGGAGCGCGGCGGGCCGGGCCGAGAGACCCC CCGAGCGCATCGCAGGGAGGACCCGAGGGCGGGGCGGAGCGCGGCGGGCCGGGCCGAGAGACCCC T C TMEM240 Ensembl:ENSG00000205090 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1540544..1540902 26863196 MeRIP-seq:(Medium) rs1408417121 Functional Loss SNV dbSNP153 33..33 33 - - - 66932 RMVar_ID_66932 Human_SNP_ID_366024 m1A Human chr1 - 1540603 1540603 1540603 CGAGCGGAGCCGAGTCGAGCCGAGCCGAGCGCATCGCAGGGAGGACCCGAGGGCGGAGCGGAGCG CGAGCGGAGCCGAGTCGAGCCGAGCCGAGCGCGTCGCAGGGAGGACCCGAGGGCGGAGCGGAGCG T C TMEM240 Ensembl:ENSG00000205090 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1540552..1540644 26863196 MeRIP-seq:(Medium) rs1223225383 Functional Loss SNV dbSNP153 33..33 33 - - - 66933 RMVar_ID_66933 Human_SNP_ID_377653 m1A Human chr1 + 1574551 1574551 1574551 CGAGCACACCACCGCCACCCGCAGCGGGGACGACGGCATGGCGGCGGCCGCAAATCCCGCGGCTC CGAGCACACCACCGCCACCCGCAGCGGGGACGCCGGCATGGCGGCGGCCGCAAATCCCGCGGCTC A C AL645728.1 Ensembl:ENSG00000215014 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1574450..1574600 26863196 MeRIP-seq:(Medium) rs11537882 Functional Loss SNV dbSNP153 33..33 33 - - - 66934 RMVar_ID_66934 Human_SNP_ID_377685 m1A Human chr1 - 1574590 1574590 1574590 GCGCGGAAGCGCCGCGGTAGGGTGGGAACCCAAGCGGGAGAGCCGCGGGATTTGCGGCCGCCGCC GCGCGGAAGCGCCGCGGTAGGGTGGGAACCCAGGCGGGAGAGCCGCGGGATTTGCGGCCGCCGCC T C SSU72 Ensembl:ENSG00000160075 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1574576..1574600 26863196 MeRIP-seq:(Medium) rs781706092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325952,Human_RBP_ID_4073431,Human_RBP_ID_5312179,Human_RBP_ID_9318431,Human_RBP_ID_17762281,Human_RBP_ID_18473345,Human_RBP_ID_22022589,Human_RBP_ID_23121393,Human_RBP_ID_24528884,Human_RBP_ID_26841329 RMVar_hsa_circ_84662,RMVar_hsa_circ_128356,RMVar_hsa_circ_108941,RMVar_hsa_circ_128359 66935 RMVar_ID_66935 Human_SNP_ID_377765 m1A Human chr1 - 1574755 1574755 1574755 CGGCCTCGCCGAGTGCAGCGCGCCCGAAGGCCAGTGCCTGCGCTCCGTCCGCGGCCCGGCGCCCA CGGCCTCGCCGAGTGCAGCGCGCCCGAAGGCCTGTGCCTGCGCTCCGTCCGCGGCCCGGCGCCCA T A SSU72 Ensembl:ENSG00000160075 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:1574726..1574815 26863410 MeRIP-seq:(Medium) rs1253708830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1411632,Human_RBP_ID_4072428,Human_RBP_ID_8939927,Human_RBP_ID_17668293 RMVar_hsa_circ_84662,RMVar_hsa_circ_128356,RMVar_hsa_circ_108941,RMVar_hsa_circ_128359 66936 RMVar_ID_66936 Human_SNP_ID_386220 m1A Human chr1 - 1597465 1597463 1597465 AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGGAGGGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGG__GGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1597451..1597500 26863196 MeRIP-seq:(Medium) rs1426512302 Functional Loss DEL dbSNP153 33..34 33 - - - 66937 RMVar_ID_66937 Human_SNP_ID_386223 m1A Human chr1 - 1597465 1597464 1597465 AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGGAGGGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGG_GGGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1597451..1597500 26863196 MeRIP-seq:(Medium) rs1557519844 Functional Loss DEL dbSNP153 33..33 33 - - - 66938 RMVar_ID_66938 Human_SNP_ID_386224 m1A Human chr1 - 1597465 1597465 1597465 AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGGAGGGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC AAAACAGGCGGGGGGGGGGGGGGCGGAGGGGGGGGGGGAGGAGGAGCCCAGCTCTGAGGAGTGAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1597451..1597500 26863196 MeRIP-seq:(Medium) rs1044435841 Functional Loss SNV dbSNP153 33..33 33 - - - 66939 RMVar_ID_66939 Human_SNP_ID_386459 m1A Human chr1 + 1598100 1598077 1598100 GCCACGCAGGGGTGGGCGGAGCAAAGACACACAGGTGGGCTACAGGTGTCACACGGCACCAGCCA GCCACGCAGG_______________________GGTGGGCTACAGGTGTCACACGGCACCAGCCA GGGTGGGCGGAGCAAAGACACACA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1598051..1598613 26863196 MeRIP-seq:(Medium) rs1490580274 Functional Loss DEL dbSNP153 11..33 33 - - - 66940 RMVar_ID_66940 Human_SNP_ID_386819 m1A Human chr1 - 1599234 1599234 1599234 CGCTCTCCTCTCCTCATTCCTGCTGCCTCCTTAAGATCCCCGCGGAGGAGGACCTGCCGGCGACG CGCTCTCCTCTCCTCATTCCTGCTGCCTCCTTGAGATCCCCGCGGAGGAGGACCTGCCGGCGACG T C FNDC10 Ensembl:ENSG00000228594 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11552172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18551721 66941 RMVar_ID_66941 Human_SNP_ID_387101 m1A Human chr1 + 1599964 1599952 1599965 CCAGCCCGGCGGCGTCGGGGCGGCCGCGGCGCAGGGCGGCGGCGCGCAGGCGGCCAGCAGCAGCA CCAGCCCGGCGGCGTCGGGGC_____________GGCGGCGGCGCGCAGGCGGCCAGCAGCAGCA CGGCCGCGGCGCAG C LOC105378586 RNACentral:URS0000BC447D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1599920..1600019 26863196 MeRIP-seq:(Medium) rs897943550 Functional Loss DEL dbSNP153 22..34 33 - - - 66942 RMVar_ID_66942 Human_SNP_ID_387110 m1A Human chr1 + 1599987 1599985 1599988 CCGCGGCGCAGGGCGGCGGCGCGCAGGCGGCCAGCAGCAGCAGCAGCGGCGGGGCGCGCATCCTG CCGCGGCGCAGGGCGGCGGCGCGCAGGCGGC___CAGCAGCAGCAGCGGCGGGGCGCGCATCCTG CCAG C LOC105378586 RNACentral:URS0000BC447D lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:1599901..1600087;chr1:1599526..1600125 26863410 MeRIP-seq:(Medium) rs888652457 Functional Loss DEL dbSNP153 32..34 33 - - - 66943 RMVar_ID_66943 Human_SNP_ID_387113 m1A Human chr1 + 1599987 1599987 1599987 CCGCGGCGCAGGGCGGCGGCGCGCAGGCGGCCAGCAGCAGCAGCAGCGGCGGGGCGCGCATCCTG CCGCGGCGCAGGGCGGCGGCGCGCAGGCGGCCCGCAGCAGCAGCAGCGGCGGGGCGCGCATCCTG A C LOC105378586 RNACentral:URS0000BC447D lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:1599901..1600087;chr1:1599526..1600125 26863410 MeRIP-seq:(Medium) rs1007523099 Functional Loss SNV dbSNP153 33..33 33 - - - 66944 RMVar_ID_66944 Human_SNP_ID_387126 m1A Human chr1 + 1600030 1600030 1600030 CAGCGGCGGGGCGCGCATCCTGCGGCGGGGCCACGGGGCGCGGCGCTGGGTCACGCGGGCCGCGC CAGCGGCGGGGCGCGCATCCTGCGGCGGGGCCGCGGGGCGCGGCGCTGGGTCACGCGGGCCGCGC A G LOC105378586 RNACentral:URS0000BC447D lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr1:1599946..1600046;chr1:1599930..1600126 26863410 MeRIP-seq:(Medium) rs1489626980 Functional Loss SNV dbSNP153 33..33 33 - - - 66945 RMVar_ID_66945 Human_SNP_ID_388930 m1A Human chr1 - 1605458 1605458 1605458 CCAGACAATCCCTCACCTCACCACCCCACCCCACGCCTGACCACCCCACCCCACGCCTGACCAGC CCAGACAATCCCTCACCTCACCACCCCACCCCCCGCCTGACCACCCCACCCCACGCCTGACCAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1605453..1605790 26863196 MeRIP-seq:(Medium) rs1185553283 Functional Loss SNV dbSNP153 33..33 33 - - - 66946 RMVar_ID_66946 Human_SNP_ID_389024 m1A Human chr1 + 1605633 1605633 1605633 GCTGGGCTGGTCAGGTGTGGGGTCGGCTGGTCAGGTGTGGGCTGGGCTGGGCTGGTCAGGTGTGG GCTGGGCTGGTCAGGTGTGGGGTCGGCTGGTCCGGTGTGGGCTGGGCTGGGCTGGTCAGGTGTGG A C LOC105378586,lnc-MIB2-1,lnc-MIB2-1:2,LOC105378586:2,lnc-MIB2-1:3 RNACentral:URS0000BC447D,RNACentral:URS00008B3337,RNACentral:URS00008BB792,RNACentral:URS00008BC95F,RNACentral:URS00008B9AAB lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1605601..1605780 26863196 MeRIP-seq:(Medium) rs1253635894 Functional Loss SNV dbSNP153 33..33 33 - - - 66947 RMVar_ID_66947 Human_SNP_ID_389039 m1A Human chr1 - 1605668 1605649 1605669 CCTGACCAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCAGCCCACA CCTGACCAGCCCAGCCCACACCTGACCAGCC____________________CAGCCCAGCCCACA GGGCTGGTCAGGTGTGGGGTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1605664..1605798 26863196 MeRIP-seq:(Medium) rs1413675886 Functional Loss DEL dbSNP153 32..51 33 - - - 66948 RMVar_ID_66948 Human_SNP_ID_389056 m1A Human chr1 - 1605668 1605668 1605668 CCTGACCAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCAGCCCACA CCTGACCAGCCCAGCCCACACCTGACCAGCCGGCCCCACACCTGACCAGCCCAGCCCAGCCCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1605664..1605798 26863196 MeRIP-seq:(Medium) rs1192875794 Functional Loss SNV dbSNP153 33..33 33 - - - 66949 RMVar_ID_66949 Human_SNP_ID_389437 m1A Human chr1 - 1606258 1606250 1606258 CCAGCCTAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCACACCTGA CCAGCCTAGCCCAGCCCACACCTGACCAGCCG________CCTGACCAGCCCAGCCCACACCTGA GTGTGGGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1606241..1606594 26863196 MeRIP-seq:(Medium) rs1207927575 Functional Loss DEL dbSNP153 33..40 33 - - - 66950 RMVar_ID_66950 Human_SNP_ID_389440 m1A Human chr1 - 1606258 1606254 1606258 CCAGCCTAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCACACCTGA CCAGCCTAGCCCAGCCCACACCTGACCAGCCG____CACACCTGACCAGCCCAGCCCACACCTGA GGGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1606241..1606594 26863196 MeRIP-seq:(Medium) rs199723811 Functional Loss DEL dbSNP153 33..36 33 - - - 66951 RMVar_ID_66951 Human_SNP_ID_389444 m1A Human chr1 - 1606258 1606258 1606258 CCAGCCTAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCACACCTGA CCAGCCTAGCCCAGCCCACACCTGACCAGCCGGCCCCACACCTGACCAGCCCAGCCCACACCTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1606241..1606594 26863196 MeRIP-seq:(Medium) rs1473567117 Functional Loss SNV dbSNP153 33..33 33 - - - 66952 RMVar_ID_66952 Human_SNP_ID_389460 m1A Human chr1 - 1606283 1606279 1606284 CCTGACCAGCCGACCCCACACCTGACCAGCCTAGCCCAGCCCACACCTGACCAGCCGACCCCACA CCTGACCAGCCGACCCCACACCTGACCAGCC_____CAGCCCACACCTGACCAGCCGACCCCACA GGGCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1606281..1606595 26863196 MeRIP-seq:(Medium) rs201886324 Functional Loss DEL dbSNP153 32..36 33 - - - 66953 RMVar_ID_66953 Human_SNP_ID_389479 m1A Human chr1 - 1606336 1606336 1606336 AGCCCGTCCCACACCTGACCAGCCCACCCCACACCTGACCAGCCCAGCCCACACCTGACCAGCCG AGCCCGTCCCACACCTGACCAGCCCACCCCACGCCTGACCAGCCCAGCCCACACCTGACCAGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1606334..1606491 26863196 MeRIP-seq:(Medium) rs1186291415 Functional Loss SNV dbSNP153 33..33 33 - - - 66954 RMVar_ID_66954 Human_SNP_ID_389480 m1A Human chr1 - 1606336 1606336 1606336 AGCCCGTCCCACACCTGACCAGCCCACCCCACACCTGACCAGCCCAGCCCACACCTGACCAGCCG AGCCCGTCCCACACCTGACCAGCCCACCCCACCCCTGACCAGCCCAGCCCACACCTGACCAGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1606334..1606491 26863196 MeRIP-seq:(Medium) rs1186291415 Functional Loss SNV dbSNP153 33..33 33 - - - 66955 RMVar_ID_66955 Human_SNP_ID_392621 m1A Human chr1 + 1615887 1615887 1615887 AGCTCCCGGCAGGCCTCGCGCGGCCCGGGGCCAGCGGCGCTGGGGTCGGCGCTGGGGTCGTCGTC AGCTCCCGGCAGGCCTCGCGCGGCCCGGGGCCCGCGGCGCTGGGGTCGGCGCTGGGGTCGTCGTC A C MIB2 Ensembl:ENSG00000197530 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1615885..1616059 26863196 MeRIP-seq:(Medium) rs997517709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18415913 66956 RMVar_ID_66956 Human_SNP_ID_392622 m1A Human chr1 + 1615887 1615887 1615887 AGCTCCCGGCAGGCCTCGCGCGGCCCGGGGCCAGCGGCGCTGGGGTCGGCGCTGGGGTCGTCGTC AGCTCCCGGCAGGCCTCGCGCGGCCCGGGGCCGGCGGCGCTGGGGTCGGCGCTGGGGTCGTCGTC A G MIB2 Ensembl:ENSG00000197530 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1615885..1616059 26863196 MeRIP-seq:(Medium) rs997517709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18415913 66957 RMVar_ID_66957 Human_SNP_ID_392623 m1A Human chr1 - 1615900 1615888 1615900 CCCACCCGGCCCGGACGACGACCCCAGCGCCGACCCCAGCGCCGCTGGCCCCGGGCCGCGCGAGG CCCACCCGGCCCGGACGACGACCCCAGCGCCG____________CTGGCCCCGGGCCGCGCGAGG GCGGCGCTGGGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:1615872..1616205;chr1:1615893..1616130 26863196 MeRIP-seq:(Medium) rs932341363 Functional Loss DEL dbSNP153 33..44 33 - - - 66958 RMVar_ID_66958 Human_SNP_ID_395686 m1A Human chr1 + 1625116 1625116 1625116 CCACCAATGTGTACCGTGTGGGCCACAAGGGCAAGGTGGACCTCAAGTGTGTGGGCGAGGCAGCG CCACCAATGTGTACCGTGTGGGCCACAAGGGCCAGGTGGACCTCAAGTGTGTGGGCGAGGCAGCG A C MIB2 Ensembl:ENSG00000197530 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:1624956..1625123 26863196 MeRIP-seq:(Medium) rs1350523694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_4461,Human_Splice_Rec_4497,Human_Splice_Rec_4567,Human_Splice_Rec_4603,Human_Splice_Rec_4637,Human_Splice_Rec_4673,Human_Splice_Rec_4719,Human_Splice_Rec_4805,Human_Splice_Rec_4839,Human_Splice_Rec_4869,Human_Splice_Rec_4901,Human_Splice_Rec_4933,Human_Splice_Rec_4959,Human_Splice_Rec_4963 66959 RMVar_ID_66959 Human_SNP_ID_396524 m1A Human chr1 + 1626875 1626875 1626875 GGCCGCGTCGGGAAGGTGGTGAAAGTGTTTGGAGACGGGAACCTGCGTGTAGCAGTCGCTGGTCA GGCCGCGTCGGGAAGGTGGTGAAAGTGTTTGGCGACGGGAACCTGCGTGTAGCAGTCGCTGGTCA A C MIB2 Ensembl:ENSG00000197530 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1626676..1626972;chr1:1626640..1627122 26863196 MeRIP-seq:(Medium) rs756978924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934915,Human_RBP_ID_5137033,Human_RBP_ID_5156301,Human_RBP_ID_9355325 Human_Splice_Rec_4468,Human_Splice_Rec_4504,Human_Splice_Rec_4538,Human_Splice_Rec_4574,Human_Splice_Rec_4608,Human_Splice_Rec_4644,Human_Splice_Rec_4680,Human_Splice_Rec_4726,Human_Splice_Rec_4768,Human_Splice_Rec_4812,Human_Splice_Rec_4844,Human_Splice_Rec_4874,Human_Splice_Rec_4906,Human_Splice_Rec_4938,Human_Splice_Rec_4968 66960 RMVar_ID_66960 Human_SNP_ID_397259 m1A Human chr1 - 1628179 1628179 1628179 CGGCTGCAGCTGTGTGCCCACCCCACACTCACAGCGCGTGACCCTTGAGGGAGGCATGGTGCAGC CGGCTGCAGCTGTGTGCCCACCCCACACTCACGGCGCGTGACCCTTGAGGGAGGCATGGTGCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1628144..1628294 26863196 MeRIP-seq:(Medium) rs1315723435 Functional Loss SNV dbSNP153 33..33 33 - - - 66961 RMVar_ID_66961 Human_SNP_ID_397596 m1A Human chr1 + 1628720 1628720 1628720 GGGGGGACCCAGGGCCCTTGCAGCTGCTGTCCAGGGTGAGGAAGTGTGGCGTGGGGTGCTGGAGA GGGGGGACCCAGGGCCCTTGCAGCTGCTGTCCGGGGTGAGGAAGTGTGGCGTGGGGTGCTGGAGA A G MIB2 Ensembl:ENSG00000197530 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1628692..1629103 26863196 MeRIP-seq:(Medium) rs1245113615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5332514 Human_Splice_Rec_4479,Human_Splice_Rec_4515,Human_Splice_Rec_4549,Human_Splice_Rec_4585,Human_Splice_Rec_4619,Human_Splice_Rec_4655,Human_Splice_Rec_4689,Human_Splice_Rec_4737,Human_Splice_Rec_4779,Human_Splice_Rec_4823,Human_Splice_Rec_4853,Human_Splice_Rec_4885,Human_Splice_Rec_4915,Human_Splice_Rec_4949,Human_Splice_Rec_4975,Human_Splice_Rec_4985,Human_Splice_Rec_4987 66962 RMVar_ID_66962 Human_SNP_ID_398589 m1A Human chr1 - 1630424 1630424 1630424 GGGCGCATGCGCCGTGGCCGCACTGGAACACGAGGCGGATGTGGCTGTCGATGCAGATGGGGCAG GGGCGCATGCGCCGTGGCCGCACTGGAACACGGGGCGGATGTGGCTGTCGATGCAGATGGGGCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1629673..1630569 26863196 MeRIP-seq:(Medium) rs1309421856 Functional Loss SNV dbSNP153 33..33 33 - - - 66963 RMVar_ID_66963 Human_SNP_ID_398676 m1A Human chr1 - 1630556 1630556 1630556 TTATAAAACACAGGGCGGGGGCACGCGAAGGCAGCTCGGGCGCGGCGGACGGCGCGGCTCACACG TTATAAAACACAGGGCGGGGGCACGCGAAGGCTGCTCGGGCGCGGCGGACGGCGCGGCTCACACG T A HSALNG0000184 RNACentral:URS0000EC191F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1629673..1630625;chr1:1629673..1630561 26863196 MeRIP-seq:(Medium) rs971646265 Functional Loss SNV dbSNP153 33..33 33 - - - 66964 RMVar_ID_66964 Human_SNP_ID_398677 m1A Human chr1 - 1630556 1630556 1630556 TTATAAAACACAGGGCGGGGGCACGCGAAGGCAGCTCGGGCGCGGCGGACGGCGCGGCTCACACG TTATAAAACACAGGGCGGGGGCACGCGAAGGCCGCTCGGGCGCGGCGGACGGCGCGGCTCACACG T G HSALNG0000184 RNACentral:URS0000EC191F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1629673..1630625;chr1:1629673..1630561 26863196 MeRIP-seq:(Medium) rs971646265 Functional Loss SNV dbSNP153 33..33 33 - - - 66965 RMVar_ID_66965 Human_SNP_ID_401033 m1A Human chr1 - 1636431 1636431 1636431 GAGAAAATCTGGCCCGGCTACAGCGAGCTCCCAGCAGTCAAGAAGATGACCTTCAGCGAGCACCC GAGAAAATCTGGCCCGGCTACAGCGAGCTCCCGGCAGTCAAGAAGATGACCTTCAGCGAGCACCC T C CDK11B Ensembl:ENSG00000248333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1636382..1636512 26863196 MeRIP-seq:(Medium) rs757373547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25950,Human_RBP_ID_5698370,Human_RBP_ID_17675354,Human_RBP_ID_26310020 Human_Splice_Rec_5108,Human_Splice_Rec_5109,Human_Splice_Rec_5146,Human_Splice_Rec_5147,Human_Splice_Rec_5180,Human_Splice_Rec_5181,Human_Splice_Rec_5220,Human_Splice_Rec_5221,Human_Splice_Rec_5256,Human_Splice_Rec_5257,Human_Splice_Rec_5298,Human_Splice_Rec_5299,Human_Splice_Rec_5338,Human_Splice_Rec_5339,Human_Splice_Rec_5380,Human_Splice_Rec_5381 66966 RMVar_ID_66966 Human_SNP_ID_401458 m1A Human chr1 + 1637168 1637168 1637168 AGGATCCAGTTGTCGTGCAGGTGTTTCACCCCACGCAGCAGCTGGATCATCAGGGTCTTCACCTC AGGATCCAGTTGTCGTGCAGGTGTTTCACCCCCCGCAGCAGCTGGATCATCAGGGTCTTCACCTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1637082..1637182 26863196 MeRIP-seq:(Medium) rs190165683 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 66967 RMVar_ID_66967 Human_SNP_ID_401809 m1A Human chr1 - 1637805 1637805 1637805 GGGCTTCCCGATCACGTCGCTGAGGGAGATCAACACCATCCTCAAGGCCCAGCATCCCAACATCG GGGCTTCCCGATCACGTCGCTGAGGGAGATCAGCACCATCCTCAAGGCCCAGCATCCCAACATCG T C CDK11B Ensembl:ENSG00000248333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1637778..1637843;chr1:1637486..1637875 26863196 MeRIP-seq:(Medium) rs886688865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9355330,Human_RBP_ID_18522660,Human_RBP_ID_26310024 Human_Splice_Rec_5098,Human_Splice_Rec_5099,Human_Splice_Rec_5136,Human_Splice_Rec_5137,Human_Splice_Rec_5170,Human_Splice_Rec_5171,Human_Splice_Rec_5210,Human_Splice_Rec_5211,Human_Splice_Rec_5246,Human_Splice_Rec_5247,Human_Splice_Rec_5288,Human_Splice_Rec_5289,Human_Splice_Rec_5328,Human_Splice_Rec_5329,Human_Splice_Rec_5370,Human_Splice_Rec_5371 66968 RMVar_ID_66968 Human_SNP_ID_401810 m1A Human chr1 - 1637805 1637805 1637805 GGGCTTCCCGATCACGTCGCTGAGGGAGATCAACACCATCCTCAAGGCCCAGCATCCCAACATCG GGGCTTCCCGATCACGTCGCTGAGGGAGATCACCACCATCCTCAAGGCCCAGCATCCCAACATCG T G CDK11B Ensembl:ENSG00000248333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1637778..1637843;chr1:1637486..1637875 26863196 MeRIP-seq:(Medium) rs886688865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9355330,Human_RBP_ID_18522660,Human_RBP_ID_26310024 Human_Splice_Rec_5098,Human_Splice_Rec_5099,Human_Splice_Rec_5136,Human_Splice_Rec_5137,Human_Splice_Rec_5170,Human_Splice_Rec_5171,Human_Splice_Rec_5210,Human_Splice_Rec_5211,Human_Splice_Rec_5246,Human_Splice_Rec_5247,Human_Splice_Rec_5288,Human_Splice_Rec_5289,Human_Splice_Rec_5328,Human_Splice_Rec_5329,Human_Splice_Rec_5370,Human_Splice_Rec_5371 66969 RMVar_ID_66969 Human_SNP_ID_403688 m1A Human chr1 - 1642499 1642499 1642499 TCCCTCTCTGCCCTGCGCGCCAGTGTCTGCACATCACCGAACGATGAGAGAGGACTACAGCGACA TCCCTCTCTGCCCTGCGCGCCAGTGTCTGCACGTCACCGAACGATGAGAGAGGACTACAGCGACA T C CDK11B Ensembl:ENSG00000248333 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1254451635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_5086,Human_Splice_Rec_5124,Human_Splice_Rec_5198,Human_Splice_Rec_5234,Human_Splice_Rec_5276,Human_Splice_Rec_5316,Human_Splice_Rec_5358,Human_Splice_Rec_5396 RMVar_hsa_circ_53930 66970 RMVar_ID_66970 Human_SNP_ID_409603 m1A Human chr1 + 1658854 1658854 1658854 GTCCGCCCCGCTCCGAGGCCTGCTCGGAAGAAAGACCTCGGTGCGCAGTTCTCCTCGCGCTCCCA GTCCGCCCCGCTCCGAGGCCTGCTCGGAAGAAGGACCTCGGTGCGCAGTTCTCCTCGCGCTCCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1658852..1658960 26863410 MeRIP-seq:(Medium) rs1257861419 Functional Loss SNV dbSNP153 33..33 33 - - - 66971 RMVar_ID_66971 Human_SNP_ID_409641 m1A Human chr1 - 1658931 1658922 1658931 CTGGCTCCGGGACCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGTAGGGGTGAGTTCCGACTGG CTGGCTCCGGGACCGGCGGCGGCGGCGGCGGC_________GGCGTAGGGGTGAGTTCCGACTGG CGCCGCCGCT C CDK11B Ensembl:ENSG00000248333 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1657447..1658966 26863196 MeRIP-seq:(Medium) rs994453275 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_223295,Human_RBP_ID_804690,Human_RBP_ID_4073436,Human_RBP_ID_9357880,Human_RBP_ID_18414820,Human_RBP_ID_19033622,Human_RBP_ID_26310040 Human_Splice_Rec_5075,Human_Splice_Rec_5113,Human_Splice_Rec_5151,Human_Splice_Rec_5185,Human_Splice_Rec_5225,Human_Splice_Rec_5261,Human_Splice_Rec_5303,Human_Splice_Rec_5343,Human_Splice_Rec_5385 66972 RMVar_ID_66972 Human_SNP_ID_409648 m1A Human chr1 - 1658931 1658931 1658931 CTGGCTCCGGGACCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGTAGGGGTGAGTTCCGACTGG CTGGCTCCGGGACCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGTAGGGGTGAGTTCCGACTGG T C CDK11B Ensembl:ENSG00000248333 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1657447..1658966 26863196 MeRIP-seq:(Medium) rs1048742069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223295,Human_RBP_ID_804690,Human_RBP_ID_4073436,Human_RBP_ID_9357880,Human_RBP_ID_18414820,Human_RBP_ID_19033622,Human_RBP_ID_26310040 Human_Splice_Rec_5075,Human_Splice_Rec_5113,Human_Splice_Rec_5151,Human_Splice_Rec_5185,Human_Splice_Rec_5225,Human_Splice_Rec_5261,Human_Splice_Rec_5303,Human_Splice_Rec_5343,Human_Splice_Rec_5385 66973 RMVar_ID_66973 Human_SNP_ID_409756 m1A Human chr1 + 1659119 1659119 1659119 GCACTTCCTGTGTCTGCGCGGGATGATAACGCATAAAACAGCGCTTGCTCAGGTCCAGGACGCCA GCACTTCCTGTGTCTGCGCGGGATGATAACGCCTAAAACAGCGCTTGCTCAGGTCCAGGACGCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1659116..1659210 26863196 MeRIP-seq:(Medium) rs967893891 Functional Loss SNV dbSNP153 33..33 33 - - - 66974 RMVar_ID_66974 Human_SNP_ID_411404 m1A Human chr1 - 1664101 1664101 1664101 TTGGCTCACTGCAGCCTCGACTTCCTGGGCTCAAATGATCCTCCCACCTCAGCCTCCCATGTGGC TTGGCTCACTGCAGCCTCGACTTCCTGGGCTCCAATGATCCTCCCACCTCAGCCTCCCATGTGGC T G SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1461739814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26387147,Human_RBP_ID_27169947 66975 RMVar_ID_66975 Human_SNP_ID_424711 m1A Human chr1 - 1704095 1704095 1704095 CGCGGGAGTACGGATCCCCTCTGAAGGCCTACACCCCGGTCGTGGTGACCCAGTGGTACCGCGCC CGCGGGAGTACGGATCCCCTCTGAAGGCCTACGCCCCGGTCGTGGTGACCCAGTGGTACCGCGCC T C AL031282.2,CDK11A Ensembl:ENSG00000268575,Ensembl:ENSG00000008128 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1704089..1704238 26863196 MeRIP-seq:(Medium) rs1292096698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438746,Human_RBP_ID_5543759,Human_RBP_ID_18966870,Human_RBP_ID_22632693,Human_RBP_ID_26310044,Human_RBP_ID_27799553 Human_Splice_Rec_5502,Human_Splice_Rec_5503,Human_Splice_Rec_5538,Human_Splice_Rec_5539,Human_Splice_Rec_5548,Human_Splice_Rec_5549,Human_Splice_Rec_5579,Human_Splice_Rec_5616,Human_Splice_Rec_5617,Human_Splice_Rec_5652,Human_Splice_Rec_5653,Human_Splice_Rec_5690,Human_Splice_Rec_5691,Human_Splice_Rec_5728,Human_Splice_Rec_5729,Human_Splice_Rec_5766,Human_Splice_Rec_5767,Human_Splice_Rec_5804,Human_Splice_Rec_5805,Human_Splice_Rec_5813,Human_Splice_Rec_5822,Human_Splice_Rec_5823,Human_Splice_Rec_5838,Human_Splice_Rec_5842 Human_miRNA_ID_2018181,Human_miRNA_ID_2018182,Human_miRNA_ID_2018183,Human_miRNA_ID_2170580,Human_miRNA_ID_2170581,Human_miRNA_ID_2170582 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_106150,RMVar_hsa_circ_128372 66976 RMVar_ID_66976 Human_SNP_ID_425434 m1A Human chr1 - 1705648 1705645 1705649 CCTATGGAGTGGTCTACAGAGCAAAAGACAAGAAAACAGGTGGGTGGGGTCCCCTCACCCCACAA CCTATGGAGTGGTCTACAGAGCAAAAGACAA____ACAGGTGGGTGGGGTCCCCTCACCCCACAA TTTTC T AL031282.2,CDK11A Ensembl:ENSG00000268575,Ensembl:ENSG00000008128 lincRNA,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1705645..1707421 26863196 MeRIP-seq:(Medium) rs754605532 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5541815 Human_Splice_Rec_5494,Human_Splice_Rec_5495,Human_Splice_Rec_5530,Human_Splice_Rec_5531,Human_Splice_Rec_5572,Human_Splice_Rec_5573,Human_Splice_Rec_5608,Human_Splice_Rec_5609,Human_Splice_Rec_5644,Human_Splice_Rec_5645,Human_Splice_Rec_5682,Human_Splice_Rec_5683,Human_Splice_Rec_5720,Human_Splice_Rec_5721,Human_Splice_Rec_5758,Human_Splice_Rec_5759,Human_Splice_Rec_5796,Human_Splice_Rec_5797,Human_Splice_Rec_5832,Human_Splice_Rec_5833,Human_Splice_Rec_5850,Human_Splice_Rec_5851,Human_Splice_Rec_5856,Human_Splice_Rec_5857,Human_Splice_Rec_5896,Human_Splice_Rec_5897 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_1885 66977 RMVar_ID_66977 Human_SNP_ID_425435 m1A Human chr1 - 1705648 1705646 1705649 CCTATGGAGTGGTCTACAGAGCAAAAGACAAGAAAACAGGTGGGTGGGGTCCCCTCACCCCACAA CCTATGGAGTGGTCTACAGAGCAAAAGACAA___AACAGGTGGGTGGGGTCCCCTCACCCCACAA TTTC T AL031282.2,CDK11A Ensembl:ENSG00000268575,Ensembl:ENSG00000008128 lincRNA,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1705645..1707421 26863196 MeRIP-seq:(Medium) rs1253368650 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5541815 Human_Splice_Rec_5494,Human_Splice_Rec_5495,Human_Splice_Rec_5530,Human_Splice_Rec_5531,Human_Splice_Rec_5572,Human_Splice_Rec_5573,Human_Splice_Rec_5608,Human_Splice_Rec_5609,Human_Splice_Rec_5644,Human_Splice_Rec_5645,Human_Splice_Rec_5682,Human_Splice_Rec_5683,Human_Splice_Rec_5720,Human_Splice_Rec_5721,Human_Splice_Rec_5758,Human_Splice_Rec_5759,Human_Splice_Rec_5796,Human_Splice_Rec_5797,Human_Splice_Rec_5832,Human_Splice_Rec_5833,Human_Splice_Rec_5850,Human_Splice_Rec_5851,Human_Splice_Rec_5856,Human_Splice_Rec_5857,Human_Splice_Rec_5896,Human_Splice_Rec_5897 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_1885 66978 RMVar_ID_66978 Human_SNP_ID_430604 m1A Human chr1 - 1721607 1721607 1721607 ATAAGGAACTCCCCGTATAGAAGAGAAGACTCAATGGAAGACAGGTGAGCGGATGTACAGATGTG ATAAGGAACTCCCCGTATAGAAGAGAAGACTCTATGGAAGACAGGTGAGCGGATGTACAGATGTG T A AL031282.2,CDK11A Ensembl:ENSG00000268575,Ensembl:ENSG00000008128 lincRNA,Protein coding exon,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438754,Human_RBP_ID_3333954,Human_RBP_ID_4077545,Human_RBP_ID_5536774,Human_RBP_ID_23341089,Human_RBP_ID_26310055,Human_RBP_ID_27799560 Human_Splice_Rec_5477,Human_Splice_Rec_5513,Human_Splice_Rec_5555,Human_Splice_Rec_5591,Human_Splice_Rec_5627,Human_Splice_Rec_5665,Human_Splice_Rec_5703,Human_Splice_Rec_5741,Human_Splice_Rec_5779,Human_Splice_Rec_5863,Human_Splice_Rec_5867,Human_Splice_Rec_5879 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_48797,RMVar_hsa_circ_333572,RMVar_hsa_circ_361449 66979 RMVar_ID_66979 Human_SNP_ID_433206 m1A Human chr1 - 1729287 1729287 1729287 AGGGTGGCCTTGTCCACCTCCCCATCGAGAATATGGCTGCCGGCCTCTTTGAAGATTGTGGTCTG AGGGTGGCCTTGTCCACCTCCCCATCGAGAATGTGGCTGCCGGCCTCTTTGAAGATTGTGGTCTG T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1061884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_366952,Human_RBP_ID_1073977,Human_RBP_ID_4005516,Human_RBP_ID_10635608,Human_RBP_ID_23145342,Human_RBP_ID_26370974 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 66980 RMVar_ID_66980 Human_SNP_ID_433214 m1A Human chr1 - 1729296 1729296 1729296 GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCATCGAGAATATGGCTGCCGGCCTCTTTGAAGAT GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCTTCGAGAATATGGCTGCCGGCCTCTTTGAAGAT T A SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1061883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1073977,Human_RBP_ID_5541855,Human_RBP_ID_5897308,Human_RBP_ID_8171533,Human_RBP_ID_10635609,Human_RBP_ID_23145342,Human_RBP_ID_26370974 Human_miRNA_ID_2365616,Human_miRNA_ID_2365617,Human_miRNA_ID_3013421,Human_miRNA_ID_3013422 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 66981 RMVar_ID_66981 Human_SNP_ID_433215 m1A Human chr1 - 1729296 1729296 1729296 GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCATCGAGAATATGGCTGCCGGCCTCTTTGAAGAT GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCGTCGAGAATATGGCTGCCGGCCTCTTTGAAGAT T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1061883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1073977,Human_RBP_ID_5541855,Human_RBP_ID_5897308,Human_RBP_ID_8171533,Human_RBP_ID_10635609,Human_RBP_ID_23145342,Human_RBP_ID_26370974 Human_miRNA_ID_2365616,Human_miRNA_ID_2365617,Human_miRNA_ID_3013421,Human_miRNA_ID_3013422 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 66982 RMVar_ID_66982 Human_SNP_ID_433250 m1A Human chr1 - 1729416 1729414 1729416 AGATCGTGCCATTGCACTCCAGCCTGGGCAACAGGGCAAGATTCCGTCTCAAAAACAAACACTAT AGATCGTGCCATTGCACTCCAGCCTGGGCAAC__GGCAAGATTCCGTCTCAAAAACAAACACTAT CCT C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1244097531 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 66983 RMVar_ID_66983 Human_SNP_ID_435711 m1A Human chr1 + 1736835 1736828 1736836 AAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAAAAAAAAAAAAGGAAGTTATCATAATCTTTGT AAAAAAAAAAAAAAAAAGAAAGAAAG________AAAAAAAAAAGGAAGTTATCATAATCTTTGT GAAAGAAAA G AL031282.1 Ensembl:ENSG00000227775 Pseudogene intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:1736790..1736876 26863410 MeRIP-seq:(Medium) rs1391121477 Functional Loss DEL dbSNP153 27..34 33 - - - 66984 RMVar_ID_66984 Human_SNP_ID_438820 m1A Human chr1 - 1746225 1746225 1746225 CGGGCTGGACCACCAGGCGGCCGCGGAGAGGCACTTAAAAGCCCCGTGTTACCCTAGACCTTAAA CGGGCTGGACCACCAGGCGGCCGCGGAGAGGCCCTTAAAAGCCCCGTGTTACCCTAGACCTTAAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1746152..1746262 26863196 MeRIP-seq:(Medium) rs1460036380 Functional Loss SNV dbSNP153 33..33 33 - - - 66985 RMVar_ID_66985 Human_SNP_ID_440581 m1A Human chr1 - 1751739 1751739 1751739 TTTTTTGAGTAACTGCTCTCTGAGTTTTGCACACGAAGTTGCCCTCATCTGCTGGAGATCGATAA TTTTTTGAGTAACTGCTCTCTGAGTTTTGCACCCGAAGTTGCCCTCATCTGCTGGAGATCGATAA T G NADK Ensembl:ENSG00000008130 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1751679..1751779 32194978 MeRIP-seq:(Medium) rs1223568451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332388,Human_RBP_ID_2103152,Human_RBP_ID_8958065,Human_RBP_ID_10646073,Human_RBP_ID_18555571,Human_RBP_ID_22849805 Human_miRNA_ID_2179652,Human_miRNA_ID_2181757 RMVar_hsa_circ_119731,RMVar_hsa_circ_128381 66986 RMVar_ID_66986 Human_SNP_ID_445256 m1A Human chr1 - 1765327 1765327 1765327 AGACGCGGCTGCTTACTGCTGCTCGGCCTGCCACGGCGATGAGACCTGGAGTTACAACCACCCCA AGACGCGGCTGCTTACTGCTGCTCGGCCTGCCGCGGCGATGAGACCTGGAGTTACAACCACCCCA T C NADK Ensembl:ENSG00000008130 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr1:1765276..1765481;chr1:1765276..1778299 26863196,32194978 MeRIP-seq:(Medium) rs961640986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332630,Human_RBP_ID_746070,Human_RBP_ID_4074993,Human_RBP_ID_8290041,Human_RBP_ID_8737806,Human_RBP_ID_10648762,Human_RBP_ID_22871139 Human_Splice_Rec_5973,Human_Splice_Rec_5993,Human_Splice_Rec_6013,Human_Splice_Rec_6111,Human_Splice_Rec_6119,Human_Splice_Rec_6125,Human_Splice_Rec_6131 RMVar_hsa_circ_18407,RMVar_hsa_circ_8494,RMVar_hsa_circ_38147,RMVar_hsa_circ_274767 66987 RMVar_ID_66987 Human_SNP_ID_448984 m1A Human chr1 - 1778386 1778386 1778386 GCGGCCATGGGGCAACAGGCGGCCAGGGCGCCAAGGGCCAGGTAGCGACGGCTGGCGGCGGCGCG GCGGCCATGGGGCAACAGGCGGCCAGGGCGCCGAGGGCCAGGTAGCGACGGCTGGCGGCGGCGCG T C NADK Ensembl:ENSG00000008130 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr1:1778266..1778450;chr1:1778217..1778475 26863410,26863196 MeRIP-seq:(Medium) rs959119783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072435,Human_RBP_ID_5136034,Human_RBP_ID_5642098,Human_RBP_ID_17668294,Human_RBP_ID_18415238,Human_RBP_ID_18455342,Human_RBP_ID_22562002,Human_RBP_ID_27835052 Human_Splice_Rec_5971,Human_Splice_Rec_6117,Human_Splice_Rec_6123,Human_Splice_Rec_6129 66988 RMVar_ID_66988 Human_SNP_ID_448988 m1A Human chr1 - 1778394 1778394 1778394 GGGTCCGGGCGGCCATGGGGCAACAGGCGGCCAGGGCGCCAAGGGCCAGGTAGCGACGGCTGGCG GGGTCCGGGCGGCCATGGGGCAACAGGCGGCCGGGGCGCCAAGGGCCAGGTAGCGACGGCTGGCG T C NADK Ensembl:ENSG00000008130 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1778191..1778475 26863196 MeRIP-seq:(Medium) rs1244825661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072435,Human_RBP_ID_5136034,Human_RBP_ID_17668294,Human_RBP_ID_18415238,Human_RBP_ID_18455342,Human_RBP_ID_22562002,Human_RBP_ID_27391016,Human_RBP_ID_27835052 66989 RMVar_ID_66989 Human_SNP_ID_448989 m1A Human chr1 - 1778394 1778394 1778394 GGGTCCGGGCGGCCATGGGGCAACAGGCGGCCAGGGCGCCAAGGGCCAGGTAGCGACGGCTGGCG GGGTCCGGGCGGCCATGGGGCAACAGGCGGCCCGGGCGCCAAGGGCCAGGTAGCGACGGCTGGCG T G NADK Ensembl:ENSG00000008130 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1778191..1778475 26863196 MeRIP-seq:(Medium) rs1244825661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072435,Human_RBP_ID_5136034,Human_RBP_ID_17668294,Human_RBP_ID_18415238,Human_RBP_ID_18455342,Human_RBP_ID_22562002,Human_RBP_ID_27391016,Human_RBP_ID_27835052 66990 RMVar_ID_66990 Human_SNP_ID_451117 m1A Human chr1 - 1785576 1785576 1785576 GGTTCTGTGGGACCCCCCGCCCCGCCCCCCGCACTCCTTCATAGCAGCAGTAGTGGCTTCTCCAT GGTTCTGTGGGACCCCCCGCCCCGCCCCCCGCCCTCCTTCATAGCAGCAGTAGTGGCTTCTCCAT T G GNB1 Ensembl:ENSG00000078369 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1785407..1785750 26863196 MeRIP-seq:(Medium) rs1258091970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332902,Human_RBP_ID_5158903,Human_RBP_ID_5713289,Human_RBP_ID_17213800,Human_RBP_ID_17337915,Human_RBP_ID_18219687,Human_RBP_ID_21962115,Human_RBP_ID_26371845 Human_miRNA_ID_94005 RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_117153,RMVar_hsa_circ_96576,RMVar_hsa_circ_128386,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_88726,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128387 66991 RMVar_ID_66991 Human_SNP_ID_451134 m1A Human chr1 - 1785597 1785597 1785597 AGCAGCAGCGTTTGGAAAGCAGGTTCTGTGGGACCCCCCGCCCCGCCCCCCGCACTCCTTCATAG AGCAGCAGCGTTTGGAAAGCAGGTTCTGTGGGCCCCCCCGCCCCGCCCCCCGCACTCCTTCATAG T G GNB1 Ensembl:ENSG00000078369 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1785369..1785750;chr1:1785426..1785775 31548705,26863196 m1A-IP-seq:(High) rs952010029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332902,Human_RBP_ID_5713289,Human_RBP_ID_10654145,Human_RBP_ID_17213802,Human_RBP_ID_17337915,Human_RBP_ID_24448412,Human_RBP_ID_26387155 Human_miRNA_ID_2145825,Human_miRNA_ID_2386207,Human_miRNA_ID_2387679,Human_miRNA_ID_2398837,Human_miRNA_ID_2987262,Human_miRNA_ID_3020950,Human_miRNA_ID_3029883,Human_miRNA_ID_3065260 RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_117153,RMVar_hsa_circ_96576,RMVar_hsa_circ_128386,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_88726,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128387 66992 RMVar_ID_66992 Human_SNP_ID_451135 m1A Human chr1 + 1785601 1785601 1785601 GAAGGAGTGCGGGGGGCGGGGCGGGGGGTCCCACAGAACCTGCTTTCCAAACGCTGCTGCTGAAC GAAGGAGTGCGGGGGGCGGGGCGGGGGGTCCCGCAGAACCTGCTTTCCAAACGCTGCTGCTGAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1785551..1785733 32194978 MeRIP-seq:(Medium) rs1167756826 Functional Loss SNV dbSNP153 33..33 33 - - - 66993 RMVar_ID_66993 Human_SNP_ID_451221 m1A Human chr1 - 1785889 1785889 1785889 TCTGTCCACTTCTCGTTGCTGCTCTGTGGCACATATCGGAAGCAGTACAGCGCGCGGCTCTACAC TCTGTCCACTTCTCGTTGCTGCTCTGTGGCACGTATCGGAAGCAGTACAGCGCGCGGCTCTACAC T C GNB1 Ensembl:ENSG00000078369 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs946402468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332943,Human_RBP_ID_1071800,Human_RBP_ID_1729288,Human_RBP_ID_4008085,Human_RBP_ID_5713317,Human_RBP_ID_8958403,Human_RBP_ID_10654161,Human_RBP_ID_17213811,Human_RBP_ID_17337917,Human_RBP_ID_17447611,Human_RBP_ID_18219696,Human_RBP_ID_19446161,Human_RBP_ID_21962116,Human_RBP_ID_22781180,Human_RBP_ID_23145505,Human_RBP_ID_26371854,Human_RBP_ID_27171653 Human_miRNA_ID_455073,Human_miRNA_ID_457026,Human_miRNA_ID_1330797,Human_miRNA_ID_2147692,Human_miRNA_ID_2148491,Human_miRNA_ID_2657991 RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_117153,RMVar_hsa_circ_96576,RMVar_hsa_circ_128386,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_88726,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128387 66994 RMVar_ID_66994 Human_SNP_ID_452018 m1A Human chr1 - 1789054 1789054 1789054 AACGTCTGGGATGCACTCAAAGCCGACCGGGCAGGTACGTGGCCATGGGGCCTTTCTGTGTCTTG AACGTCTGGGATGCACTCAAAGCCGACCGGGCGGGTACGTGGCCATGGGGCCTTTCTGTGTCTTG T C GNB1 Ensembl:ENSG00000078369 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1789051..1789100 32194978 MeRIP-seq:(Medium) rs779971509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17223644,Human_RBP_ID_19033649,Human_RBP_ID_26797482 Human_Splice_Rec_6153,Human_Splice_Rec_6171,Human_Splice_Rec_6193 RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_96576,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128397,RMVar_hsa_circ_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_376755,RMVar_hsa_circ_369314,RMVar_hsa_circ_94091,RMVar_hsa_circ_104378,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_128398,RMVar_hsa_circ_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_128396,RMVar_hsa_circ_320759,RMVar_hsa_circ_279629,RMVar_hsa_circ_89721,RMVar_hsa_circ_128401,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402 66995 RMVar_ID_66995 Human_SNP_ID_459580 m1A Human chr1 - 1815976 1815976 1815976 GCCACAGTGGAAGCCACTGGAGAACTGTGGGAAGGGCTGGGAAGAGGTAGGCACAGTGGGCGAGC GCCACAGTGGAAGCCACTGGAGAACTGTGGGAGGGGCTGGGAAGAGGTAGGCACAGTGGGCGAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1815974..1816171 26863196 MeRIP-seq:(Medium) rs561849474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23263418 RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_128398,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_128405,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_276555,RMVar_hsa_circ_276074,RMVar_hsa_circ_270649,RMVar_hsa_circ_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_128417,RMVar_hsa_circ_128425,RMVar_hsa_circ_291736,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_282800,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128429,RMVar_hsa_circ_128430 66996 RMVar_ID_66996 Human_SNP_ID_466052 m1A Human chr1 + 1839223 1839223 1839223 TTAATTCAGAAGGGCTTCTGGTCTGGTCTCCAATACATGTAAATTTGTCTGAAACAAACAGAAAA TTAATTCAGAAGGGCTTCTGGTCTGGTCTCCAGTACATGTAAATTTGTCTGAAACAAACAGAAAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1839201..1839250 26863196 MeRIP-seq:(Medium) rs947907306 Functional Loss SNV dbSNP153 33..33 33 - - - 66997 RMVar_ID_66997 Human_SNP_ID_481598 m1A Human chr1 + 1890001 1890001 1890001 GGCCTTCGGAATATCGCAAACCGGGCCCCGAAACTCGGCGCGGCGGCGGCCGCCCCACAAAGGCA GGCCTTCGGAATATCGCAAACCGGGCCCCGAACCTCGGCGCGGCGGCGGCCGCCCCACAAAGGCA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1889996..1890199 26863196 MeRIP-seq:(Medium) rs1343065616 Functional Loss SNV dbSNP153 33..33 33 - - - 66998 RMVar_ID_66998 Human_SNP_ID_482015 m1A Human chr1 - 1890969 1890969 1890969 CGGCGAGTGGGGAGCGGGGCCGGGAGTGGAGCAGCCGCCGCGGCGGGACTGGACCGAGCCTCGCC CGGCGAGTGGGGAGCGGGGCCGGGAGTGGAGCGGCCGCCGCGGCGGGACTGGACCGAGCCTCGCC T C GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:1890751..1891100 26863196 MeRIP-seq:(Medium) rs1394118226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17672,Human_RBP_ID_95903,Human_RBP_ID_221180,Human_RBP_ID_334954,Human_RBP_ID_801145,Human_RBP_ID_858611,Human_RBP_ID_3327971,Human_RBP_ID_3934932,Human_RBP_ID_4011615,Human_RBP_ID_5108956,Human_RBP_ID_5136036,Human_RBP_ID_5725028,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410375,Human_RBP_ID_18414823,Human_RBP_ID_18927781,Human_RBP_ID_22427994,Human_RBP_ID_22531354,Human_RBP_ID_22532023,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 66999 RMVar_ID_66999 Human_SNP_ID_482021 m1A Human chr1 - 1891007 1890983 1891007 ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGG________________________GCCGGGAGT CCCCGCTCCCCACTCGCCGCCCGCT C GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1890920..1891073 26863410 MeRIP-seq:(Medium) rs981606261 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3329326,Human_RBP_ID_4011617,Human_RBP_ID_5136578,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410889,Human_RBP_ID_18414823,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67000 RMVar_ID_67000 Human_SNP_ID_482028 m1A Human chr1 - 1890996 1890996 1890996 GGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGTGGAGCAGCCGC GGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGGGTGGGGAGCGGGGCCGGGAGTGGAGCAGCCGC T C GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:1890801..1891100 26863196 MeRIP-seq:(Medium) rs1307741030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3327971,Human_RBP_ID_4011615,Human_RBP_ID_5108956,Human_RBP_ID_5136578,Human_RBP_ID_5725029,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410375,Human_RBP_ID_18414823,Human_RBP_ID_18927781,Human_RBP_ID_22427994,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67001 RMVar_ID_67001 Human_SNP_ID_482029 m1A Human chr1 - 1890996 1890996 1890996 GGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGTGGAGCAGCCGC GGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGCGTGGGGAGCGGGGCCGGGAGTGGAGCAGCCGC T G GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:1890801..1891100 26863196 MeRIP-seq:(Medium) rs1307741030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3327971,Human_RBP_ID_4011615,Human_RBP_ID_5108956,Human_RBP_ID_5136578,Human_RBP_ID_5725029,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410375,Human_RBP_ID_18414823,Human_RBP_ID_18927781,Human_RBP_ID_22427994,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67002 RMVar_ID_67002 Human_SNP_ID_482034 m1A Human chr1 - 1891007 1891001 1891007 ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGG______CGGCGAGTGGGGAGCGGGGCCGGGAGT GCCCGCT G GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1890920..1891073 26863410 MeRIP-seq:(Medium) rs981741012 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3329326,Human_RBP_ID_4011617,Human_RBP_ID_5136578,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410889,Human_RBP_ID_18414823,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67003 RMVar_ID_67003 Human_SNP_ID_482039 m1A Human chr1 - 1891007 1891007 1891007 ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGGGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT T C GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1890920..1891073 26863410 MeRIP-seq:(Medium) rs867147349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3329326,Human_RBP_ID_4011617,Human_RBP_ID_5136578,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410889,Human_RBP_ID_18414823,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67004 RMVar_ID_67004 Human_SNP_ID_482040 m1A Human chr1 - 1891007 1891007 1891007 ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGAGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT ACGGAGGCGGCGGCGGCGGCGGCGGGAGCGGGCGCGGGCGGCGAGTGGGGAGCGGGGCCGGGAGT T G GNB1 Ensembl:ENSG00000078369 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:1890920..1891073 26863410 MeRIP-seq:(Medium) rs867147349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95903,Human_RBP_ID_801145,Human_RBP_ID_3329326,Human_RBP_ID_4011617,Human_RBP_ID_5136578,Human_RBP_ID_8939932,Human_RBP_ID_9318453,Human_RBP_ID_9410889,Human_RBP_ID_18414823,Human_RBP_ID_22531354,Human_RBP_ID_22532024,Human_RBP_ID_26773803 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 67005 RMVar_ID_67005 Human_SNP_ID_487465 m1A Human chr1 - 1909275 1909275 1909275 CGGATCACCCGGCCCCGCCCCGTCACCCGGCCACGCCCCGTCATCCGGCCACGCCCCGTCACTTC CGGATCACCCGGCCCCGCCCCGTCACCCGGCCGCGCCCCGTCATCCGGCCACGCCCCGTCACTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1909267..1909408 26863196 MeRIP-seq:(Medium) rs562966514 Functional Loss SNV dbSNP153 33..33 33 - - - 67006 RMVar_ID_67006 Human_SNP_ID_487466 m1A Human chr1 - 1909275 1909275 1909275 CGGATCACCCGGCCCCGCCCCGTCACCCGGCCACGCCCCGTCATCCGGCCACGCCCCGTCACTTC CGGATCACCCGGCCCCGCCCCGTCACCCGGCCCCGCCCCGTCATCCGGCCACGCCCCGTCACTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1909267..1909408 26863196 MeRIP-seq:(Medium) rs562966514 Functional Loss SNV dbSNP153 33..33 33 - - - 67007 RMVar_ID_67007 Human_SNP_ID_534039 m1A Human chr1 + 2050502 2050502 2050502 GCCCCGCGCGCCGCCGGAGTTCCGCGGAGTTGACCGGGTCGGCGCCGTCGGTCCTGAGCGCTGCC GCCCCGCGCGCCGCCGGAGTTCCGCGGAGTTGGCCGGGTCGGCGCCGTCGGTCCTGAGCGCTGCC A G PRKCZ Ensembl:ENSG00000067606 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:2050426..2050575 26863410 MeRIP-seq:(Medium) rs1346115365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4015708,Human_RBP_ID_8294425 RMVar_hsa_circ_100385,RMVar_hsa_circ_128441 67008 RMVar_ID_67008 Human_SNP_ID_534067 m1A Human chr1 - 2050543 2050543 2050543 CGGGGCGGGGGCTCCAGGTGGGGCCGCGGCGGAACGCGGAAGGCAGCGCTCAGGACCGACGGCGC CGGGGCGGGGGCTCCAGGTGGGGCCGCGGCGGGACGCGGAAGGCAGCGCTCAGGACCGACGGCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2050442..2050600 26863410 MeRIP-seq:(Medium) rs1341965919 Functional Loss SNV dbSNP153 33..33 33 - - - 67009 RMVar_ID_67009 Human_SNP_ID_534096 m1A Human chr1 - 2050591 2050591 2050591 TCCCCCCGCCGCCGTCAGCGCTGCGCCCCGGGAGCTCCGGCCATGGCGCGGGGCGGGGGCTCCAG TCCCCCCGCCGCCGTCAGCGCTGCGCCCCGGGGGCTCCGGCCATGGCGCGGGGCGGGGGCTCCAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2050512..2050694 26863196 MeRIP-seq:(Medium) rs1357922948 Functional Loss SNV dbSNP153 33..33 33 - - - 67010 RMVar_ID_67010 Human_SNP_ID_537289 m1A Human chr1 - 2059625 2059625 2059625 GGCACAACGGATCAACAGTTCAACCCCGTAACATGCGAGACCGGCGTAGGAAACCCCAGTACTCA GGCACAACGGATCAACAGTTCAACCCCGTAACGTGCGAGACCGGCGTAGGAAACCCCAGTACTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2059620..2059715 26863196 MeRIP-seq:(Medium) rs1179341097 Functional Loss SNV dbSNP153 33..33 33 - - - 67011 RMVar_ID_67011 Human_SNP_ID_537572 m1A Human chr1 + 2060490 2060425 2060491 GGGCTGAATAGAGGTTTGGCAGTGCTTAGCATAGGGGGCGAGAGTCTCGGCTTCCAGCGAGAAGT __________________________________GGGGCGAGAGTCTCGGCTTCCAGCGAGAAGT TGGGGCGAGAGTCTTGGCTTCCAGTGAGAAGTGGGGCTGAATAGAGGTTTGGCAGTGCTTAGCATAG T PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2060486..2060905 26863196 MeRIP-seq:(Medium) rs1557477979 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_3329349 RMVar_hsa_circ_28890 67012 RMVar_ID_67012 Human_SNP_ID_537592 m1A Human chr1 + 2060490 2060489 2060490 GGGCTGAATAGAGGTTTGGCAGTGCTTAGCATAGGGGGCGAGAGTCTCGGCTTCCAGCGAGAAGT GGGCTGAATAGAGGTTTGGCAGTGCTTAGCAT_GGGGGCGAGAGTCTCGGCTTCCAGCGAGAAGT TA T PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2060486..2060905 26863196 MeRIP-seq:(Medium) rs1178004435 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3329349 RMVar_hsa_circ_28890 67013 RMVar_ID_67013 Human_SNP_ID_557153 m1A Human chr1 + 2121506 2121506 2121506 AGTTAGTTAGGGTCACGGTGGTAGTTAGGATCATGGTGGTACTTAAGGTCATGGCAGTAGTTAGG AGTTAGTTAGGGTCACGGTGGTAGTTAGGATCGTGGTGGTACTTAAGGTCATGGCAGTAGTTAGG A G PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:2121436..2121703;chr1:2121497..2121680 26863196 MeRIP-seq:(Medium) rs1229226233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801540,Human_RBP_ID_17102698 RMVar_hsa_circ_28890 67014 RMVar_ID_67014 Human_SNP_ID_557331 m1A Human chr1 - 2121666 2121653 2121666 TAACCACCACCGTGACCCTAACCACCACCACGACCCTAACCACCACCGTGACCCTAACTACCACT TAACCACCACCGTGACCCTAACCACCACCACG_____________CCGTGACCCTAACTACCACT GTGGTGGTTAGGGT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:2121576..2121698 26863196 MeRIP-seq:(Medium) rs1431102341 Functional Loss DEL dbSNP153 33..45 33 - - - 67015 RMVar_ID_67015 Human_SNP_ID_557341 m1A Human chr1 - 2121666 2121664 2121667 TAACCACCACCGTGACCCTAACCACCACCACGACCCTAACCACCACCGTGACCCTAACTACCACT TAACCACCACCGTGACCCTAACCACCACCAC___CCTAACCACCACCGTGACCCTAACTACCACT GGTC G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:2121576..2121698 26863196 MeRIP-seq:(Medium) rs1345702375 Functional Loss DEL dbSNP153 32..34 33 - - - 67016 RMVar_ID_67016 Human_SNP_ID_557602 m1A Human chr1 + 2121904 2121886 2121904 AGGGTCACGGTGGTGGTTAGGGTCACGGTGGTAGTTAGGGTCACGGCTGTAGTTAGCGTCATGGT AGGGTCACGGTGGTG__________________GTTAGGGTCACGGCTGTAGTTAGCGTCATGGT GGTTAGGGTCACGGTGGTA G PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:2121853..2121966 26863196 MeRIP-seq:(Medium) rs1212835701 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_24176,Human_RBP_ID_800655,Human_RBP_ID_17102699 RMVar_hsa_circ_28890 67017 RMVar_ID_67017 Human_SNP_ID_557615 m1A Human chr1 + 2121904 2121904 2121904 AGGGTCACGGTGGTGGTTAGGGTCACGGTGGTAGTTAGGGTCACGGCTGTAGTTAGCGTCATGGT AGGGTCACGGTGGTGGTTAGGGTCACGGTGGTGGTTAGGGTCACGGCTGTAGTTAGCGTCATGGT A G PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:2121853..2121966 26863196 MeRIP-seq:(Medium) rs185975756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24176,Human_RBP_ID_800655,Human_RBP_ID_17102699 RMVar_hsa_circ_28890 67018 RMVar_ID_67018 Human_SNP_ID_557620 m1A Human chr1 - 2121933 2121913 2121934 CCCTAACCACCGCCGTGACCCTAACCACCACCATGACGCTAACTACAGCCGTGACCCTAACTACC CCCTAACCACCGCCGTGACCCTAACCACCAC_____________________GACCCTAACTACC CACGGCTGTAGTTAGCGTCATG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2121854..2122124 26863196 MeRIP-seq:(Medium) rs1371712840 Functional Loss DEL dbSNP153 32..52 33 - - - 67019 RMVar_ID_67019 Human_SNP_ID_557626 m1A Human chr1 - 2121919 2121919 2121919 GTGACCCTAACCACCACCATGACGCTAACTACAGCCGTGACCCTAACTACCACCGTGACCCTAAC GTGACCCTAACCACCACCATGACGCTAACTACCGCCGTGACCCTAACTACCACCGTGACCCTAAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:2121817..2122028 26863196 MeRIP-seq:(Medium) rs1251879148 Functional Loss SNV dbSNP153 33..33 33 - - - 67020 RMVar_ID_67020 Human_SNP_ID_557631 m1A Human chr1 + 2121926 2121926 2121926 TCACGGTGGTAGTTAGGGTCACGGCTGTAGTTAGCGTCATGGTGGTGGTTAGGGTCACGGCGGTG TCACGGTGGTAGTTAGGGTCACGGCTGTAGTTGGCGTCATGGTGGTGGTTAGGGTCACGGCGGTG A G PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2121864..2122140 26863196 MeRIP-seq:(Medium) rs796372852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800655,Human_RBP_ID_17102699 RMVar_hsa_circ_28890 67021 RMVar_ID_67021 Human_SNP_ID_557634 m1A Human chr1 - 2121933 2121931 2121934 CCCTAACCACCGCCGTGACCCTAACCACCACCATGACGCTAACTACAGCCGTGACCCTAACTACC CCCTAACCACCGCCGTGACCCTAACCACCAC___GACGCTAACTACAGCCGTGACCCTAACTACC CATG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2121854..2122124 26863196 MeRIP-seq:(Medium) rs1557614609 Functional Loss DEL dbSNP153 32..34 33 - - - 67022 RMVar_ID_67022 Human_SNP_ID_557636 m1A Human chr1 - 2121933 2121933 2121933 CCCTAACCACCGCCGTGACCCTAACCACCACCATGACGCTAACTACAGCCGTGACCCTAACTACC CCCTAACCACCGCCGTGACCCTAACCACCACCGTGACGCTAACTACAGCCGTGACCCTAACTACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2121854..2122124 26863196 MeRIP-seq:(Medium) rs867632219 Functional Loss SNV dbSNP153 33..33 33 - - - 67023 RMVar_ID_67023 Human_SNP_ID_557638 m1A Human chr1 - 2121936 2121936 2121936 TGACCCTAACCACCGCCGTGACCCTAACCACCACCATGACGCTAACTACAGCCGTGACCCTAACT TGACCCTAACCACCGCCGTGACCCTAACCACCGCCATGACGCTAACTACAGCCGTGACCCTAACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2121857..2121980 26863196 MeRIP-seq:(Medium) rs1374500084 Functional Loss SNV dbSNP153 33..33 33 - - - 67024 RMVar_ID_67024 Human_SNP_ID_558453 m1A Human chr1 - 2122951 2122933 2122951 TGACCCTAACCACCACCATGACCCTAACTACCACCGTGACCCTAACCACCGCCGTGACCCTAACC TGACCCTAACCACCACCATGACCCTAACTACC__________________GCCGTGACCCTAACC CGGTGGTTAGGGTCACGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2122920..2122988;chr1:2122906..2123022 26863196 MeRIP-seq:(Medium) rs1182432636 Functional Loss DEL dbSNP153 33..50 33 - - - 67025 RMVar_ID_67025 Human_SNP_ID_558475 m1A Human chr1 - 2122951 2122951 2122951 TGACCCTAACCACCACCATGACCCTAACTACCACCGTGACCCTAACCACCGCCGTGACCCTAACC TGACCCTAACCACCACCATGACCCTAACTACCGCCGTGACCCTAACCACCGCCGTGACCCTAACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2122920..2122988;chr1:2122906..2123022 26863196 MeRIP-seq:(Medium) rs796937157 Functional Loss SNV dbSNP153 33..33 33 - - - 67026 RMVar_ID_67026 Human_SNP_ID_558478 m1A Human chr1 - 2122954 2122954 2122954 CCGTGACCCTAACCACCACCATGACCCTAACTACCACCGTGACCCTAACCACCGCCGTGACCCTA CCGTGACCCTAACCACCACCATGACCCTAACTCCCACCGTGACCCTAACCACCGCCGTGACCCTA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2122893..2123021 26863196 MeRIP-seq:(Medium) rs1464580685 Functional Loss SNV dbSNP153 33..33 33 - - - 67027 RMVar_ID_67027 Human_SNP_ID_559465 m1A Human chr1 - 2124192 2124192 2124192 GTGACGCTAACTACAGCCGTGACCCTAACTACAGCCGTGACCCTAACCACCGCCGTGACCCTAAC GTGACGCTAACTACAGCCGTGACCCTAACTACCGCCGTGACCCTAACCACCGCCGTGACCCTAAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2124159..2124316 26863196 MeRIP-seq:(Medium) rs78366091 Functional Loss SNV dbSNP153 33..33 33 - - - 67028 RMVar_ID_67028 Human_SNP_ID_559552 m1A Human chr1 - 2124282 2124282 2124282 GTGACCCTAACTACCACCGTGACGCTAACTACAGCCGTGACCCTAACTACCGCCATGACCCTAAC GTGACCCTAACTACCACCGTGACGCTAACTACTGCCGTGACCCTAACTACCGCCATGACCCTAAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2124146..2124342;chr1:2124128..2124327 26863196 MeRIP-seq:(Medium) rs796962776 Functional Loss SNV dbSNP153 33..33 33 - - - 67029 RMVar_ID_67029 Human_SNP_ID_559553 m1A Human chr1 - 2124282 2124282 2124282 GTGACCCTAACTACCACCGTGACGCTAACTACAGCCGTGACCCTAACTACCGCCATGACCCTAAC GTGACCCTAACTACCACCGTGACGCTAACTACCGCCGTGACCCTAACTACCGCCATGACCCTAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2124146..2124342;chr1:2124128..2124327 26863196 MeRIP-seq:(Medium) rs796962776 Functional Loss SNV dbSNP153 33..33 33 - - - 67030 RMVar_ID_67030 Human_SNP_ID_559555 m1A Human chr1 + 2124285 2124285 2124285 AGGGTCATGGCGGTAGTTAGGGTCACGGCTGTAGTTAGCGTCACGGTGGTAGTTAGGGTCACGGT AGGGTCATGGCGGTAGTTAGGGTCACGGCTGTGGTTAGCGTCACGGTGGTAGTTAGGGTCACGGT A G PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2124152..2124352 26863196 MeRIP-seq:(Medium) rs1477630291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28890 67031 RMVar_ID_67031 Human_SNP_ID_569338 m1A Human chr1 + 2155193 2155191 2155194 GAGGTAGTGGTGATGACGTGGTGGTGGTGATGAAGATGTTGATGATGGCGGTGATGATGGTGATG GAGGTAGTGGTGATGACGTGGTGGTGGTGAT___GATGTTGATGATGGCGGTGATGATGGTGATG TGAA T PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2155191..2155601 26863196 MeRIP-seq:(Medium) rs1457419139 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_58641,RMVar_hsa_circ_71189,RMVar_hsa_circ_28890,RMVar_hsa_circ_283431,RMVar_hsa_circ_128444,RMVar_hsa_circ_346753,RMVar_hsa_circ_354548 67032 RMVar_ID_67032 Human_SNP_ID_569363 m1A Human chr1 - 2155234 2155233 2155235 ATCCTCAATGTCATCACTACCACCACCATCACAGTCATCGCCATCACCATCATCACCGCCATCAT ATCCTCAATGTCATCACTACCACCACCATCA__GTCATCGCCATCACCATCATCACCGCCATCAT CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2155226..2155377 26863196 MeRIP-seq:(Medium) rs373383442 Functional Loss DEL dbSNP153 32..33 33 - - - 67033 RMVar_ID_67033 Human_SNP_ID_571065 m1A Human chr1 + 2160716 2160716 2160716 GGCCTGGAGGGAAGCCTTAGGGGGTGGGGAGGAGGGGCCTGTCCCCATGTGGGGGAGTCACCCCG GGCCTGGAGGGAAGCCTTAGGGGGTGGGGAGGCGGGGCCTGTCCCCATGTGGGGGAGTCACCCCG A C PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2160698..2160781 26863196 MeRIP-seq:(Medium) rs564654036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3329480,Human_RBP_ID_8166289,Human_RBP_ID_18927808 RMVar_hsa_circ_58641,RMVar_hsa_circ_71189,RMVar_hsa_circ_128448,RMVar_hsa_circ_323914 67034 RMVar_ID_67034 Human_SNP_ID_571066 m1A Human chr1 + 2160716 2160716 2160716 GGCCTGGAGGGAAGCCTTAGGGGGTGGGGAGGAGGGGCCTGTCCCCATGTGGGGGAGTCACCCCG GGCCTGGAGGGAAGCCTTAGGGGGTGGGGAGGTGGGGCCTGTCCCCATGTGGGGGAGTCACCCCG A T PRKCZ Ensembl:ENSG00000067606 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2160698..2160781 26863196 MeRIP-seq:(Medium) rs564654036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3329480,Human_RBP_ID_8166289,Human_RBP_ID_18927808 RMVar_hsa_circ_58641,RMVar_hsa_circ_71189,RMVar_hsa_circ_128448,RMVar_hsa_circ_323914 67035 RMVar_ID_67035 Human_SNP_ID_578626 m1A Human chr1 - 2184573 2184572 2184573 GGGAGCGCCTGCTTCTTCTCCAGCTTGGAAAAACAATAGGAGAAGGGTCAGCTCCGCGCGGGCAT GGGAGCGCCTGCTTCTTCTCCAGCTTGGAAAA_CAATAGGAGAAGGGTCAGCTCCGCGCGGGCAT GT G FAAP20 Ensembl:ENSG00000162585 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2184560..2184660 32194978 MeRIP-seq:(Medium) rs761527109 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_128450,RMVar_hsa_circ_76932 67036 RMVar_ID_67036 Human_SNP_ID_579893 m1A Human chr1 + 2187811 2187802 2187811 CGCCCAGAGTTCCCGCCCAGCTCGCCCAGGGCACCGTCAGTCCCGTGGGTGTGGACAGGCACGTG CGCCCAGAGTTCCCGCCCAGCTCG_________CCGTCAGTCCCGTGGGTGTGGACAGGCACGTG GCCCAGGGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2187704..2187889 26863196 MeRIP-seq:(Medium) rs1168865472 Functional Loss DEL dbSNP153 25..33 33 - - - 67037 RMVar_ID_67037 Human_SNP_ID_580612 m1A Human chr1 + 2189664 2189664 2189664 GGAGCCGAGAGGCGGGGCTGCTGGCGGGGGAGAGCGTGTCCGGGCGCCGCACTCTGCGCAGGGCT GGAGCCGAGAGGCGGGGCTGCTGGCGGGGGAGCGCGTGTCCGGGCGCCGCACTCTGCGCAGGGCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2189616..2189832 26863196 MeRIP-seq:(Medium) rs1408809424 Functional Loss SNV dbSNP153 33..33 33 - - - 67038 RMVar_ID_67038 Human_SNP_ID_580634 m1A Human chr1 + 2189682 2189682 2189682 TGCTGGCGGGGGAGAGCGTGTCCGGGCGCCGCACTCTGCGCAGGGCTCTTGGATGGCGCTCACCA TGCTGGCGGGGGAGAGCGTGTCCGGGCGCCGCGCTCTGCGCAGGGCTCTTGGATGGCGCTCACCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2187183..2189820 32194978 MeRIP-seq:(Medium) rs375854012 Functional Loss SNV dbSNP153 33..33 33 - - - 67039 RMVar_ID_67039 Human_SNP_ID_580687 m1A Human chr1 + 2189763 2189763 2189763 CTTTCGGCCAAGCACTGGGCCAGGTGGCTGTCAACATCCAGCTGGGTCAGCCTGCAAGGGAGGGG CTTTCGGCCAAGCACTGGGCCAGGTGGCTGTCCACATCCAGCTGGGTCAGCCTGCAAGGGAGGGG A C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:2189669..2189770 26863410 MeRIP-seq:(Medium) rs1166700850 Functional Loss SNV dbSNP153 33..33 33 - - - 67040 RMVar_ID_67040 Human_SNP_ID_580693 m1A Human chr1 + 2189770 2189770 2189770 CCAAGCACTGGGCCAGGTGGCTGTCAACATCCAGCTGGGTCAGCCTGCAAGGGAGGGGCCACACT CCAAGCACTGGGCCAGGTGGCTGTCAACATCCGGCTGGGTCAGCCTGCAAGGGAGGGGCCACACT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2189668..2189824 26863410 MeRIP-seq:(Medium) rs759556719 Functional Loss SNV dbSNP153 33..33 33 - - - 67041 RMVar_ID_67041 Human_SNP_ID_581966 m1A Human chr1 + 2193689 2193689 2193689 TGGCACATGGGGCAGCTGCGCAGGGCCGCGGCACCCTCCACAGACGGCTGCTGCTCCACCCTGGG TGGCACATGGGGCAGCTGCGCAGGGCCGCGGCGCCCTCCACAGACGGCTGCTGCTCCACCCTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2193589..2193921;chr1:2193607..2193942 26863196 MeRIP-seq:(Medium) rs1047360016 Functional Loss SNV dbSNP153 33..33 33 - - - 67042 RMVar_ID_67042 Human_SNP_ID_581980 m1A Human chr1 - 2193705 2193705 2193705 TGATCCCTGCAGGGCCCCCAGGGTGGAGCAGCAGCCGTCTGTGGAGGGTGCCGCGGCCCTGCGCA TGATCCCTGCAGGGCCCCCAGGGTGGAGCAGCGGCCGTCTGTGGAGGGTGCCGCGGCCCTGCGCA T C FAAP20 Ensembl:ENSG00000162585 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:2193626..2193925 26863196 MeRIP-seq:(Medium) rs373336716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073446,Human_RBP_ID_5108387,Human_RBP_ID_5136037,Human_RBP_ID_17646827,Human_RBP_ID_18966893,Human_RBP_ID_21879604 Human_Splice_Rec_7131,Human_Splice_Rec_7145,Human_Splice_Rec_7151,Human_Splice_Rec_7165,Human_Splice_Rec_7177,Human_Splice_Rec_7183,Human_Splice_Rec_7189,Human_Splice_Rec_7195,Human_Splice_Rec_7207,Human_Splice_Rec_7211,Human_Splice_Rec_7215,Human_Splice_Rec_7223 RMVar_hsa_circ_93855,RMVar_hsa_circ_128450,RMVar_hsa_circ_76932,RMVar_hsa_circ_44414,RMVar_hsa_circ_128452 67043 RMVar_ID_67043 Human_SNP_ID_581997 m1A Human chr1 - 2193740 2193740 2193740 TCCCCCGCCAGGTCCCTGCCCCAGCGCCCGGCACCTGATCCCTGCAGGGCCCCCAGGGTGGAGCA TCCCCCGCCAGGTCCCTGCCCCAGCGCCCGGCTCCTGATCCCTGCAGGGCCCCCAGGGTGGAGCA T A FAAP20 Ensembl:ENSG00000162585 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2193626..2193951 26863410 MeRIP-seq:(Medium) rs1334831487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340637,Human_RBP_ID_5136037,Human_RBP_ID_23117523 Human_miRNA_ID_2379811,Human_miRNA_ID_2379812,Human_miRNA_ID_3022830,Human_miRNA_ID_3022831 RMVar_hsa_circ_93855,RMVar_hsa_circ_128450,RMVar_hsa_circ_76932,RMVar_hsa_circ_44414,RMVar_hsa_circ_128452 67044 RMVar_ID_67044 Human_SNP_ID_581998 m1A Human chr1 - 2193740 2193740 2193740 TCCCCCGCCAGGTCCCTGCCCCAGCGCCCGGCACCTGATCCCTGCAGGGCCCCCAGGGTGGAGCA TCCCCCGCCAGGTCCCTGCCCCAGCGCCCGGCGCCTGATCCCTGCAGGGCCCCCAGGGTGGAGCA T C FAAP20 Ensembl:ENSG00000162585 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2193626..2193951 26863410 MeRIP-seq:(Medium) rs1334831487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340637,Human_RBP_ID_5136037,Human_RBP_ID_23117523 Human_miRNA_ID_2379811,Human_miRNA_ID_2379812,Human_miRNA_ID_3022830,Human_miRNA_ID_3022831 RMVar_hsa_circ_93855,RMVar_hsa_circ_128450,RMVar_hsa_circ_76932,RMVar_hsa_circ_44414,RMVar_hsa_circ_128452 67045 RMVar_ID_67045 Human_SNP_ID_582195 m1A Human chr1 + 2194129 2194129 2194129 ACCCCCCAGGAGAAACCAGGGGCGGCCGCCAGAAGGCCTGGGGCAGACAGAGAGGGCAGACAGGG ACCCCCCAGGAGAAACCAGGGGCGGCCGCCAGGAGGCCTGGGGCAGACAGAGAGGGCAGACAGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2193976..2194176 26863410 MeRIP-seq:(Medium) rs761066785 Functional Loss SNV dbSNP153 33..33 33 - - - 67046 RMVar_ID_67046 Human_SNP_ID_582321 m1A Human chr1 - 2194479 2194479 2194479 CACCCCACGCCGAGCTTCCCCCGCGCCGCCCCAGGCCCTCCCGCGCCTCTCCCATCATCGCGTCT CACCCCACGCCGAGCTTCCCCCGCGCCGCCCCGGGCCCTCCCGCGCCTCTCCCATCATCGCGTCT T C FAAP20 Ensembl:ENSG00000162585 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:2194469..2194632 26863196 MeRIP-seq:(Medium) rs1264939754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3329489,Human_RBP_ID_5125070,Human_RBP_ID_5336632,Human_RBP_ID_17072143,Human_RBP_ID_18929121 RMVar_hsa_circ_128450,RMVar_hsa_circ_76932 67047 RMVar_ID_67047 Human_SNP_ID_582349 m1A Human chr1 - 2194561 2194561 2194561 GGGAGGGCTCCCTGCCCCCGGGCCCGGCCCCCACGCCCGTCGCCCCACCCCGCGCCGCCATTCAG GGGAGGGCTCCCTGCCCCCGGGCCCGGCCCCCCCGCCCGTCGCCCCACCCCGCGCCGCCATTCAG T G FAAP20 Ensembl:ENSG00000162585 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:2194548..2194736 26863410 MeRIP-seq:(Medium) rs950128299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743868,Human_RBP_ID_5125071,Human_RBP_ID_17070954,Human_RBP_ID_26773513,Human_RBP_ID_27835055 RMVar_hsa_circ_128450,RMVar_hsa_circ_76932 67048 RMVar_ID_67048 Human_SNP_ID_582450 m1A Human chr1 - 2194716 2194716 2194716 TGGAGGCGGCGCGGAGGCCGCGGCTGGGGTTGAGCCGCCGGAGGCCGCGCCCGGCGGGCGGGTGA TGGAGGCGGCGCGGAGGCCGCGGCTGGGGTTGGGCCGCCGGAGGCCGCGCCCGGCGGGCGGGTGA T C FAAP20 Ensembl:ENSG00000162585 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:2193618..2194775;chr1:2193625..2194775 26863196 MeRIP-seq:(Medium) rs1253383706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222713,Human_RBP_ID_802567,Human_RBP_ID_4022444,Human_RBP_ID_5086080,Human_RBP_ID_5108960,Human_RBP_ID_5136040,Human_RBP_ID_5233743,Human_RBP_ID_5312209,Human_RBP_ID_5336633,Human_RBP_ID_9318460,Human_RBP_ID_18415766,Human_RBP_ID_26773823 Human_Splice_Rec_7129,Human_Splice_Rec_7147,Human_Splice_Rec_7161,Human_Splice_Rec_7173,Human_Splice_Rec_7181,Human_Splice_Rec_7185,Human_Splice_Rec_7213,Human_Splice_Rec_7219 RMVar_hsa_circ_128450,RMVar_hsa_circ_76932 67049 RMVar_ID_67049 Human_SNP_ID_585776 m1A Human chr1 - 2206113 2206113 2206113 AGACAGGTGGGTGAGTACCAACAGGGAAGTGAACTAACAGGGAAAGGCCCTGCCCCCCTCCCATG AGACAGGTGGGTGAGTACCAACAGGGAAGTGAGCTAACAGGGAAAGGCCCTGCCCCCCTCCCATG T C FAAP20 Ensembl:ENSG00000162585 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2205983..2206135 26863196 MeRIP-seq:(Medium) rs1454473733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128450,RMVar_hsa_circ_76932 67050 RMVar_ID_67050 Human_SNP_ID_586367 m1A Human chr1 - 2207925 2207925 2207925 GGACACACACACACACACACACACACACACACACACACACACACACACGGGTGTTACCAAAACGG GGACACACACACACACACACACACACACACACGCACACACACACACACGGGTGTTACCAAAACGG T C FAAP20 Ensembl:ENSG00000162585 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:2207868..2207952 26863410 MeRIP-seq:(Medium) rs879926512 Functional Loss SNV dbSNP153 33..33 33 - - - 67051 RMVar_ID_67051 Human_SNP_ID_589137 m1A Human chr1 + 2215409 2215409 2215409 CAAGGGGCGTCCATGCAGAGGCGGAGAGCAGGAGGTGAGGGGTTGGGCCCCTGGGATGGCTTGGT CAAGGGGCGTCCATGCAGAGGCGGAGAGCAGGTGGTGAGGGGTTGGGCCCCTGGGATGGCTTGGT A T AL590822.1 Ensembl:ENSG00000234396 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2215373..2215534 26863196 MeRIP-seq:(Medium) rs189771368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3331086 67052 RMVar_ID_67052 Human_SNP_ID_593058 m1A Human chr1 + 2228487 2228487 2228487 CCCGCGCCTAGAGCCCGGGGGGCGCGCGGGGGACGCGCGGGGGGCCCGGGCGGCGGCGGGCGCGG CCCGCGCCTAGAGCCCGGGGGGCGCGCGGGGGGCGCGCGGGGGGCCCGGGCGGCGGCGGGCGCGG A G SKI Ensembl:ENSG00000157933 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2228410..2228589 26863196 MeRIP-seq:(Medium) rs1445331221 Functional Loss SNV dbSNP153 33..33 33 - - - 67053 RMVar_ID_67053 Human_SNP_ID_593195 m1A Human chr1 + 2228781 2228781 2228781 GGGGAGCCGGAGCGCACCATGGAGGCGGCGGCAGGCGGCCGCGGCTGTTTCCAGCCGCACCCGGG GGGGAGCCGGAGCGCACCATGGAGGCGGCGGCGGGCGGCCGCGGCTGTTTCCAGCCGCACCCGGG A G SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2228730..2229255 26863196 MeRIP-seq:(Medium) rs1202073334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932544,Human_RBP_ID_4072446,Human_RBP_ID_5234213,Human_RBP_ID_5312210,Human_RBP_ID_8166299,Human_RBP_ID_8724773,Human_RBP_ID_9269552,Human_RBP_ID_9318461,Human_RBP_ID_9342474,Human_RBP_ID_9352350,Human_RBP_ID_17646234,Human_RBP_ID_17668058,Human_RBP_ID_18186762,Human_RBP_ID_18455365,Human_RBP_ID_22135038,Human_RBP_ID_22427995,Human_RBP_ID_22534741,Human_RBP_ID_22706506,Human_RBP_ID_22871552,Human_RBP_ID_26772916,Human_RBP_ID_27393901 67054 RMVar_ID_67054 Human_SNP_ID_593609 m1A Human chr1 + 2229577 2229565 2229577 TGGTGCACTCGCACAAGGCCCTGGAGAACCGGACCTGCCACTGGGGCTTCGACTCGGCCAACTGG TGGTGCACTCGCACAAGGCCC____________CCTGCCACTGGGGCTTCGACTCGGCCAACTGG CTGGAGAACCGGA C SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2229526..2229725 26863196 MeRIP-seq:(Medium) rs1553190052 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_25337,Human_RBP_ID_8743102,Human_RBP_ID_9357913,Human_RBP_ID_26852532,Human_RBP_ID_27175333,Human_RBP_ID_27393921 67055 RMVar_ID_67055 Human_SNP_ID_593613 m1A Human chr1 + 2229577 2229574 2229577 TGGTGCACTCGCACAAGGCCCTGGAGAACCGGACCTGCCACTGGGGCTTCGACTCGGCCAACTGG TGGTGCACTCGCACAAGGCCCTGGAGAACC___CCTGCCACTGGGGCTTCGACTCGGCCAACTGG CGGA C SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2229526..2229725 26863196 MeRIP-seq:(Medium) rs866043661 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_25337,Human_RBP_ID_8743102,Human_RBP_ID_9357913,Human_RBP_ID_26852532,Human_RBP_ID_27175333,Human_RBP_ID_27393921 67056 RMVar_ID_67056 Human_SNP_ID_593615 m1A Human chr1 + 2229577 2229577 2229577 TGGTGCACTCGCACAAGGCCCTGGAGAACCGGACCTGCCACTGGGGCTTCGACTCGGCCAACTGG TGGTGCACTCGCACAAGGCCCTGGAGAACCGGCCCTGCCACTGGGGCTTCGACTCGGCCAACTGG A C SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2229526..2229725 26863196 MeRIP-seq:(Medium) rs201274840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25337,Human_RBP_ID_8743102,Human_RBP_ID_9357913,Human_RBP_ID_26852532,Human_RBP_ID_27175333,Human_RBP_ID_27393921 67057 RMVar_ID_67057 Human_SNP_ID_609951 m1A Human chr1 + 2280636 2280624 2280636 GAAGATGCCCGAGAAGACAGGCGGCGGCGGCGATCTTCAGAGAGAGGACACCCGAGAAGACAGGC GAAGATGCCCGAGAAGACAGG____________TCTTCAGAGAGAGGACACCCGAGAAGACAGGC GCGGCGGCGGCGA G SKI Ensembl:ENSG00000157933 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2280596..2280696 26863196 MeRIP-seq:(Medium) rs1427880887 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_22707873 67058 RMVar_ID_67058 Human_SNP_ID_609955 m1A Human chr1 + 2280636 2280627 2280636 GAAGATGCCCGAGAAGACAGGCGGCGGCGGCGATCTTCAGAGAGAGGACACCCGAGAAGACAGGC GAAGATGCCCGAGAAGACAGGCGG_________TCTTCAGAGAGAGGACACCCGAGAAGACAGGC GCGGCGGCGA G SKI Ensembl:ENSG00000157933 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2280596..2280696 26863196 MeRIP-seq:(Medium) rs1177289208 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_22707873 67059 RMVar_ID_67059 Human_SNP_ID_609959 m1A Human chr1 + 2280636 2280630 2280636 GAAGATGCCCGAGAAGACAGGCGGCGGCGGCGATCTTCAGAGAGAGGACACCCGAGAAGACAGGC GAAGATGCCCGAGAAGACAGGCGGCGG______TCTTCAGAGAGAGGACACCCGAGAAGACAGGC GCGGCGA G SKI Ensembl:ENSG00000157933 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2280596..2280696 26863196 MeRIP-seq:(Medium) rs1451195425 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_22707873 67060 RMVar_ID_67060 Human_SNP_ID_617889 m1A Human chr1 + 2303060 2303060 2303060 TTCCCAGTCCCCCGCGCCTTCCGAAAAGGACAAGCCGTCCAGCTGGCTGCGGACCTTGGCCGGCT TTCCCAGTCCCCCGCGCCTTCCGAAAAGGACAGGCCGTCCAGCTGGCTGCGGACCTTGGCCGGCT A G SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2302956..2303115 26863196 MeRIP-seq:(Medium) rs745512128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1421425,Human_RBP_ID_1737252,Human_RBP_ID_18966897 Human_Splice_Rec_7234,Human_Splice_Rec_7235,Human_Splice_Rec_7246,Human_Splice_Rec_7247 Human_miRNA_ID_2253782 RMVar_hsa_circ_128454,RMVar_hsa_circ_347563,RMVar_hsa_circ_324318 67061 RMVar_ID_67061 Human_SNP_ID_618282 m1A Human chr1 - 2303927 2303927 2303927 TCGGGGGCCCGGGAGACGGCGGCGGCACACGGAGGGCTGCTCACAACCTTCTGCTGGGCCGGCGG TCGGGGGCCCGGGAGACGGCGGCGGCACACGGGGGGCTGCTCACAACCTTCTGCTGGGCCGGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2303830..2304042;chr1:2303824..2304075 26863196 MeRIP-seq:(Medium) rs1337456769 Functional Loss SNV dbSNP153 33..33 33 - - - 67062 RMVar_ID_67062 Human_SNP_ID_618299 m1A Human chr1 - 2303946 2303946 2303946 GGTGCAAGTGGCGAGAGGCTCGGGGGCCCGGGAGACGGCGGCGGCACACGGAGGGCTGCTCACAA GGTGCAAGTGGCGAGAGGCTCGGGGGCCCGGGGGACGGCGGCGGCACACGGAGGGCTGCTCACAA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:2303864..2303987 26863196 MeRIP-seq:(Medium) rs1184378281 Functional Loss SNV dbSNP153 33..33 33 - - - 67063 RMVar_ID_67063 Human_SNP_ID_618318 m1A Human chr1 + 2303970 2303970 2303970 CCGCCGTCTCCCGGGCCCCCGAGCCTCTCGCCACTTGCACCCAGCCTCGGAAGCGGAAGCTGACT CCGCCGTCTCCCGGGCCCCCGAGCCTCTCGCCCCTTGCACCCAGCCTCGGAAGCGGAAGCTGACT A C SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2303830..2304075 26863196 MeRIP-seq:(Medium) rs1421529806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17215811,Human_RBP_ID_17676597 Human_miRNA_ID_2712018,Human_miRNA_ID_3048007 RMVar_hsa_circ_47840,RMVar_hsa_circ_128454,RMVar_hsa_circ_324318,RMVar_hsa_circ_104256,RMVar_hsa_circ_128455 67064 RMVar_ID_67064 Human_SNP_ID_618320 m1A Human chr1 - 2303973 2303973 2303973 CACAGTCAGCTTCCGCTTCCGAGGCTGGGTGCAAGTGGCGAGAGGCTCGGGGGCCCGGGAGACGG CACAGTCAGCTTCCGCTTCCGAGGCTGGGTGCGAGTGGCGAGAGGCTCGGGGGCCCGGGAGACGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2303889..2306880 32194978 MeRIP-seq:(Medium) rs1224852603 Functional Loss SNV dbSNP153 33..33 33 - - - 67065 RMVar_ID_67065 Human_SNP_ID_618620 m1A Human chr1 - 2304524 2304524 2304524 CTGCGCTGAGCTTCTCCTCCTGCTTCACGCGCATCTTGACCACCTCATGCAGGAACTTCTCTTTG CTGCGCTGAGCTTCTCCTCCTGCTTCACGCGCGTCTTGACCACCTCATGCAGGAACTTCTCTTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2304474..2304549 26863196 MeRIP-seq:(Medium) rs539988362 Functional Loss SNV dbSNP153 33..33 33 - - - 67066 RMVar_ID_67066 Human_SNP_ID_619630 m1A Human chr1 - 2306644 2306644 2306644 TCTCCAGGTGCTCCCGGGCCTCGCGCTCCCGCAGCAGGTCGGCCCGCAGCTGCTCCCGGTCCGCC TCTCCAGGTGCTCCCGGGCCTCGCGCTCCCGCTGCAGGTCGGCCCGCAGCTGCTCCCGGTCCGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2306570..2306815 26863196 MeRIP-seq:(Medium) rs1280638499 Functional Loss SNV dbSNP153 33..33 33 - - - 67067 RMVar_ID_67067 Human_SNP_ID_619725 m1A Human chr1 + 2306797 2306778 2306798 GATTCCGTGCCTGCCGCCGCAGCGCCGCCGACAACGCGGGTGCAGGGGGGCGCGGCTGGGCGGTG GATTCCGTGCCTGC____________________CGCGGGTGCAGGGGGGCGCGGCTGGGCGGTG CCGCCGCAGCGCCGCCGACAA C SKI Ensembl:ENSG00000157933 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1356960548 Functional Loss DEL dbSNP153 15..34 33 - - - Human_RBP_ID_4089333 RMVar_hsa_circ_84650,RMVar_hsa_circ_128456 67068 RMVar_ID_67068 Human_SNP_ID_619749 m1A Human chr1 + 2306797 2306797 2306797 GATTCCGTGCCTGCCGCCGCAGCGCCGCCGACAACGCGGGTGCAGGGGGGCGCGGCTGGGCGGTG GATTCCGTGCCTGCCGCCGCAGCGCCGCCGACGACGCGGGTGCAGGGGGGCGCGGCTGGGCGGTG A G SKI Ensembl:ENSG00000157933 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1439908033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4089333 RMVar_hsa_circ_84650,RMVar_hsa_circ_128456 67069 RMVar_ID_67069 Human_SNP_ID_620986 m1A Human chr1 - 2309644 2309644 2309644 GGTGGGGGGGGCCGGGGCTCAGACCCACAGGGAGGAGGGGGTCACATGGGAAACGCACATGGGTT GGTGGGGGGGGCCGGGGCTCAGACCCACAGGGCGGAGGGGGTCACATGGGAAACGCACATGGGTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2309609..2309719 26863196 MeRIP-seq:(Medium) rs1030951866 Functional Loss SNV dbSNP153 33..33 33 - - - 67070 RMVar_ID_67070 Human_SNP_ID_622901 m1A Human chr1 - 2314675 2314675 2314675 GAACGGGCGTCGGGGAGGCCGCCCCGGCCCTGAGGACGCGGCGCGGGGCCCGGGACGTGCACCCC GAACGGGCGTCGGGGAGGCCGCCCCGGCCCTGGGGACGCGGCGCGGGGCCCGGGACGTGCACCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2314661..2314796 26863196 MeRIP-seq:(Medium) rs1315530085 Functional Loss SNV dbSNP153 33..33 33 - - - 67071 RMVar_ID_67071 Human_SNP_ID_625113 m1A Human chr1 + 2321239 2321239 2321239 GGAGGGCCTTGCTGCTGGCGTGGGGCCCAAGGAGCAGTGCCCTCCATAGCCGCCACTGAGCATTT GGAGGGCCTTGCTGCTGGCGTGGGGCCCAAGGTGCAGTGCCCTCCATAGCCGCCACTGAGCATTT A T AL590822.3 Ensembl:ENSG00000287356 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2321237..2321320 26863196 MeRIP-seq:(Medium) rs1035369582 Functional Loss SNV dbSNP153 33..33 33 - - - 67072 RMVar_ID_67072 Human_SNP_ID_637417 m1A Human chr1 - 2356215 2356215 2356215 CATGTCCCTGCCCAGCCCTTCCCACCACATGCAGCCCCAAGTCCCCTGAAGGCCTCTCCCCAGGA CATGTCCCTGCCCAGCCCTTCCCACCACATGCGGCCCCAAGTCCCCTGAAGGCCTCTCCCCAGGA T C MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2356210..2356336 26863196 MeRIP-seq:(Medium) rs1198320908 Functional Loss SNV dbSNP153 33..33 33 - - - 67073 RMVar_ID_67073 Human_SNP_ID_637800 m1A Human chr1 + 2357445 2357445 2357445 GTTTGTGAGCTCCACTTACCAAGCAGGCCACCAGGGGTGTCCTCCTGGCCATGGAGGGCACCCAA GTTTGTGAGCTCCACTTACCAAGCAGGCCACCTGGGGTGTCCTCCTGGCCATGGAGGGCACCCAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2357443..2357549 26863196 MeRIP-seq:(Medium) rs1416542562 Functional Loss SNV dbSNP153 33..33 33 - - - 67074 RMVar_ID_67074 Human_SNP_ID_645496 m1A Human chr1 - 2383973 2383973 2383973 GAGCAACGTCTCAGTGTCAGGAGGGGGCCCGGAGACAGACCCTCTGCGGTGGAGTCTGGGAGTGG GAGCAACGTCTCAGTGTCAGGAGGGGGCCCGGTGACAGACCCTCTGCGGTGGAGTCTGGGAGTGG T A MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2383922..2384059 26863196 MeRIP-seq:(Medium) rs1464069495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77260,RMVar_hsa_circ_314910,RMVar_hsa_circ_128458 67075 RMVar_ID_67075 Human_SNP_ID_645497 m1A Human chr1 - 2383973 2383973 2383973 GAGCAACGTCTCAGTGTCAGGAGGGGGCCCGGAGACAGACCCTCTGCGGTGGAGTCTGGGAGTGG GAGCAACGTCTCAGTGTCAGGAGGGGGCCCGGCGACAGACCCTCTGCGGTGGAGTCTGGGAGTGG T G MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:2383922..2384059 26863196 MeRIP-seq:(Medium) rs1464069495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77260,RMVar_hsa_circ_314910,RMVar_hsa_circ_128458 67076 RMVar_ID_67076 Human_SNP_ID_645879 m1A Human chr1 - 2385048 2385048 2385048 GCGTGTGTCCCCCAGGAACGGTGACAAGTACGACGGCGACTGGGTCCGGGACCGGCGTCAGGGAC GCGTGTGTCCCCCAGGAACGGTGACAAGTACGTCGGCGACTGGGTCCGGGACCGGCGTCAGGGAC T A MORN1 Ensembl:ENSG00000116151 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2379222..2385122 26863196 MeRIP-seq:(Medium) rs1343161316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4032553,Human_RBP_ID_18966899 Human_Splice_Rec_7270,Human_Splice_Rec_7271,Human_Splice_Rec_7294,Human_Splice_Rec_7295,Human_Splice_Rec_7318,Human_Splice_Rec_7319,Human_Splice_Rec_7339,Human_Splice_Rec_7343,Human_Splice_Rec_7354,Human_Splice_Rec_7355,Human_Splice_Rec_7364,Human_Splice_Rec_7365 RMVar_hsa_circ_77260,RMVar_hsa_circ_314910,RMVar_hsa_circ_128458,RMVar_hsa_circ_332911,RMVar_hsa_circ_352596 67077 RMVar_ID_67077 Human_SNP_ID_647066 m1A Human chr1 - 2388317 2388317 2388317 TTCTCCTGCCAGGTCACGGGAAGTTGTTATTTAAAGATGGCAGTTATTACGAAGGGGCGTTTGTG TTCTCCTGCCAGGTCACGGGAAGTTGTTATTTGAAGATGGCAGTTATTACGAAGGGGCGTTTGTG T C MORN1 Ensembl:ENSG00000116151 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2388205..2388382 26863196 MeRIP-seq:(Medium) rs758010872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5485700,Human_RBP_ID_24654203 Human_Splice_Rec_7264,Human_Splice_Rec_7265,Human_Splice_Rec_7288,Human_Splice_Rec_7289,Human_Splice_Rec_7312,Human_Splice_Rec_7313,Human_Splice_Rec_7349,Human_Splice_Rec_7358,Human_Splice_Rec_7359,Human_Splice_Rec_7369,Human_Splice_Rec_7372 RMVar_hsa_circ_77260,RMVar_hsa_circ_314910,RMVar_hsa_circ_128458,RMVar_hsa_circ_332911,RMVar_hsa_circ_352596 67078 RMVar_ID_67078 Human_SNP_ID_648129 m1A Human chr1 - 2391454 2391454 2391454 GGACCCGCCTAGGCGGCCGCCCCGGAACGGTAACGACTGCGGGCCACGGGACAGGTCGCTGGCTG GGACCCGCCTAGGCGGCCGCCCCGGAACGGTAGCGACTGCGGGCCACGGGACAGGTCGCTGGCTG T C MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2391435..2391540 26863410 MeRIP-seq:(Medium) rs1035441798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19036394,Human_RBP_ID_22557574 67079 RMVar_ID_67079 Human_SNP_ID_648168 m1A Human chr1 - 2391512 2391512 2391512 TCGGCGGCAAGATGGCAGCGGCGGGCGAGGGCACCCCGAGCTCCCGCGGGCCGCGTCGGGACCCG TCGGCGGCAAGATGGCAGCGGCGGGCGAGGGCCCCCCGAGCTCCCGCGGGCCGCGTCGGGACCCG T G MORN1 Ensembl:ENSG00000116151 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2391455..2391527 26863196 MeRIP-seq:(Medium) rs986038009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223636 Human_Splice_Rec_7261,Human_Splice_Rec_7287,Human_Splice_Rec_7309,Human_Splice_Rec_7357 67080 RMVar_ID_67080 Human_SNP_ID_648353 m1A Human chr1 + 2391875 2391875 2391875 GTGCTCGCTGCAGCTTCCCGGAGCCGGAGCGCAGCGCCTGCGGCCGCCCGTGCCCCGCCGTCCTC GTGCTCGCTGCAGCTTCCCGGAGCCGGAGCGCGGCGCCTGCGGCCGCCCGTGCCCCGCCGTCCTC A G RER1 Ensembl:ENSG00000157916 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2391826..2393190 26863196 MeRIP-seq:(Medium) rs375129429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222481,Human_RBP_ID_803638,Human_RBP_ID_4032670,Human_RBP_ID_9318509,Human_RBP_ID_22427996,Human_RBP_ID_23117608 Human_Splice_Rec_7373,Human_Splice_Rec_7383,Human_Splice_Rec_7391,Human_Splice_Rec_7403,Human_Splice_Rec_7417,Human_Splice_Rec_7419 RMVar_hsa_circ_114059,RMVar_hsa_circ_128459 67081 RMVar_ID_67081 Human_SNP_ID_648378 m1A Human chr1 - 2391937 2391914 2391937 CTTCCTGGCACCTCGCAGCTCCGCTACGGCCGAGCCGCGGTCTCCCTCACGGCCGCGGGAAGGAG CTTCCTGGCACCTCGCAGCTCCGCTACGGCCG_______________________CGGGAAGGAG GCGGCCGTGAGGGAGACCGCGGCT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2391826..2392010 26863410 MeRIP-seq:(Medium) rs1246586309 Functional Loss DEL dbSNP153 33..55 33 - - - 67082 RMVar_ID_67082 Human_SNP_ID_648387 m1A Human chr1 + 2391950 2391950 2391950 CCGTGAGGGAGACCGCGGCTCGGCCGTAGCGGAGCTGCGAGGTGCCAGGAAGGGCTGCGTGGCGC CCGTGAGGGAGACCGCGGCTCGGCCGTAGCGGTGCTGCGAGGTGCCAGGAAGGGCTGCGTGGCGC A T RER1 Ensembl:ENSG00000157916 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:2391876..2392067 26863196 MeRIP-seq:(Medium) rs982355945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072447,Human_RBP_ID_8302339,Human_RBP_ID_8939934,Human_RBP_ID_8964871,Human_RBP_ID_18414829,Human_RBP_ID_19036395,Human_RBP_ID_22871554,Human_RBP_ID_23117609 Human_Splice_Rec_7373,Human_Splice_Rec_7383,Human_Splice_Rec_7391,Human_Splice_Rec_7403,Human_Splice_Rec_7417,Human_Splice_Rec_7419 RMVar_hsa_circ_114059,RMVar_hsa_circ_128459 67083 RMVar_ID_67083 Human_SNP_ID_652276 m1A Human chr1 - 2403457 2403457 2403457 GGCTGGCGGGGAGCGGCCCGTTCCTCCCTCGCAGGCCTTGCTCCTGCCTGCCCACCTGGCACAGC GGCTGGCGGGGAGCGGCCCGTTCCTCCCTCGCCGGCCTTGCTCCTGCCTGCCCACCTGGCACAGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2403347..2403525 32194978 MeRIP-seq:(Medium) rs1206728173 Functional Loss SNV dbSNP153 33..33 33 - - - 67084 RMVar_ID_67084 Human_SNP_ID_654297 m1A Human chr1 + 2408825 2408825 2408825 GCACATGTATCCGCGATGGGTCCACCTGGATGATGCTGACGTACTCCTCCCCCAGGGTCTGGTAG GCACATGTATCCGCGATGGGTCCACCTGGATGCTGCTGACGTACTCCTCCCCCAGGGTCTGGTAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2408776..2408885 26863196 MeRIP-seq:(Medium) rs1286406689 Functional Loss SNV dbSNP153 33..33 33 - - - 67085 RMVar_ID_67085 Human_SNP_ID_655387 m1A Human chr1 + 2412341 2412340 2412342 CACACGGCAGACACCCCGCCTCCATGAGGGGCAACACCCCCTGGGCCGCTCGCGAGGACGTCCGG CACACGGCAGACACCCCGCCTCCATGAGGGGC__CACCCCCTGGGCCGCTCGCGAGGACGTCCGG CAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:2412334..2412499;chr1:2412339..2412503 26863196 MeRIP-seq:(Medium) rs1413964684 Functional Loss DEL dbSNP153 33..34 33 - - - 67086 RMVar_ID_67086 Human_SNP_ID_655477 m1A Human chr1 + 2412501 2412501 2412501 TCACCTCCGGGGGGCTGGCGGCGGCCGGGGCCATGGCCGCGGGTTCGGGTGGTCCCGAGCAGCCA TCACCTCCGGGGGGCTGGCGGCGGCCGGGGCCGTGGCCGCGGGTTCGGGTGGTCCCGAGCAGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2412346..2412525 26863196 MeRIP-seq:(Medium) rs724160002 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_268 67087 RMVar_ID_67087 Human_SNP_ID_674739 m1A Human chr1 - 2475376 2475376 2475376 CACCTGTGTCCTGGCCATGCCCATGCTTCGTGACCACACTGGGGAGAACCCCGCCCTTCTTCCCA CACCTGTGTCCTGGCCATGCCCATGCTTCGTGGCCACACTGGGGAGAACCCCGCCCTTCTTCCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2475374..2475528 26863196 MeRIP-seq:(Medium) rs146194335 Functional Loss SNV dbSNP153 33..33 33 - - - 67088 RMVar_ID_67088 Human_SNP_ID_684929 m1A Human chr1 + 2504484 2504484 2504484 GGCCTGGGCCGCAGCCGTGAGAACCTCGCTGGAGCCCACATGGGACGCCTGCCCCCCAGGCCCCA GGCCTGGGCCGCAGCCGTGAGAACCTCGCTGGCGCCCACATGGGACGCCTGCCCCCCAGGCCCCA A C PLCH2 Ensembl:ENSG00000149527 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2504436..2504595 26863196 MeRIP-seq:(Medium) rs1429149300 Functional Loss SNV dbSNP153 33..33 33 - - - 67089 RMVar_ID_67089 Human_SNP_ID_688670 m1A Human chr1 + 2514069 2514069 2514069 GACAGTGCTCCCTGGTGTCCAGCAGGCTGCGCACGGTCAGGGTCCCATAGGCGCTGGGGACAGAC GACAGTGCTCCCTGGTGTCCAGCAGGCTGCGCTCGGTCAGGGTCCCATAGGCGCTGGGGACAGAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2512926..2514087 32194978 MeRIP-seq:(Medium) rs769237655 Functional Loss SNV dbSNP153 33..33 33 - - - 67090 RMVar_ID_67090 Human_SNP_ID_688863 m1A Human chr1 + 2514480 2514477 2514480 CCACTGCGCGCTTCACTACCTGCCAGCGACAGAAGGAGGGGGTTAGTCAAGCGCTGGCCCTGCTG CCACTGCGCGCTTCACTACCTGCCAGCGAC___AGGAGGGGGTTAGTCAAGCGCTGGCCCTGCTG CAGA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:2514472..2514601 26863196 MeRIP-seq:(Medium) rs772575782 Functional Loss DEL dbSNP153 31..33 33 - - - 67091 RMVar_ID_67091 Human_SNP_ID_688864 m1A Human chr1 + 2514480 2514480 2514480 CCACTGCGCGCTTCACTACCTGCCAGCGACAGAAGGAGGGGGTTAGTCAAGCGCTGGCCCTGCTG CCACTGCGCGCTTCACTACCTGCCAGCGACAGGAGGAGGGGGTTAGTCAAGCGCTGGCCCTGCTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:2514472..2514601 26863196 MeRIP-seq:(Medium) rs752007394 Functional Loss SNV dbSNP153 33..33 33 - - - 67092 RMVar_ID_67092 Human_SNP_ID_689519 m1A Human chr1 + 2516120 2516120 2516120 CTGTCACCCCTACAGTTTCACCTCCTCCCGTGACCCCTGCAGTCACACTGTTCCCACCTCTGGTC CTGTCACCCCTACAGTTTCACCTCCTCCCGTGGCCCCTGCAGTCACACTGTTCCCACCTCTGGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2516081..2516158 26863196 MeRIP-seq:(Medium) rs112974410 Functional Loss SNV dbSNP153 33..33 33 - - - 67093 RMVar_ID_67093 Human_SNP_ID_690886 m1A Human chr1 - 2519803 2519803 2519803 CAGCAGCTTCGGGAAGTCGGCCACCGCCGACCAAGGTGCTCACCCCGGCCTCTGCCGCCAGAGAG CAGCAGCTTCGGGAAGTCGGCCACCGCCGACCGAGGTGCTCACCCCGGCCTCTGCCGCCAGAGAG T C PANK4 Ensembl:ENSG00000157881 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2519265..2519841 32194978 MeRIP-seq:(Medium) rs1416215956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5797507,Human_RBP_ID_18964523,Human_RBP_ID_19033697,Human_RBP_ID_26313221,Human_RBP_ID_27797282 Human_Splice_Rec_7741,Human_Splice_Rec_7775,Human_Splice_Rec_7805,Human_Splice_Rec_7873 RMVar_hsa_circ_79836,RMVar_hsa_circ_128476,RMVar_hsa_circ_110868,RMVar_hsa_circ_128484 67094 RMVar_ID_67094 Human_SNP_ID_693392 m1A Human chr1 - 2526527 2526527 2526527 GGAGCAGCGGGGACAGTCTGGACAAGAGCATCACGCTGCCCCCCGACGAGATCTTCCGCAACCTG GGAGCAGCGGGGACAGTCTGGACAAGAGCATCGCGCTGCCCCCCGACGAGATCTTCCGCAACCTG T C PANK4 Ensembl:ENSG00000157881 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:2526462..2526562 26863410 MeRIP-seq:(Medium) rs1240645726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224278,Human_RBP_ID_5537593,Human_RBP_ID_9357931,Human_RBP_ID_18429980,Human_RBP_ID_26310091,Human_RBP_ID_27797286 Human_Splice_Rec_7731,Human_Splice_Rec_7767,Human_Splice_Rec_7865,Human_Splice_Rec_7875,Human_Splice_Rec_7883 67095 RMVar_ID_67095 Human_SNP_ID_693396 m1A Human chr1 - 2526536 2526536 2526536 GCGGCAGCGGGAGCAGCGGGGACAGTCTGGACAAGAGCATCACGCTGCCCCCCGACGAGATCTTC GCGGCAGCGGGAGCAGCGGGGACAGTCTGGACGAGAGCATCACGCTGCCCCCCGACGAGATCTTC T C PANK4 Ensembl:ENSG00000157881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2526417..2526575 26863196 MeRIP-seq:(Medium) rs1459978929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5537593,Human_RBP_ID_9357931,Human_RBP_ID_26310091 Human_Splice_Rec_7731,Human_Splice_Rec_7767,Human_Splice_Rec_7865,Human_Splice_Rec_7875,Human_Splice_Rec_7883 67096 RMVar_ID_67096 Human_SNP_ID_699851 m1A Human chr1 - 2546435 2546435 2546435 GCCACGCTCTTCACTCTGGAGCACCGGCCTCAACGAGCGCGCGGGGCGGAGGGCGGCCGGGAGGC GCCACGCTCTTCACTCTGGAGCACCGGCCTCAGCGAGCGCGCGGGGCGGAGGGCGGCCGGGAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2546401..2546591 26863196 MeRIP-seq:(Medium) rs1449221455 Functional Loss SNV dbSNP153 33..33 33 - - - 67097 RMVar_ID_67097 Human_SNP_ID_712126 m1A Human chr1 + 2587216 2587215 2587217 GACCTCAGCAGCCTTGCTGGGCTCCTGGACCAACACGGCGTGCGCCTGGTGGGCGTAGGGCCCGA GACCTCAGCAGCCTTGCTGGGCTCCTGGACCA__ACGGCGTGCGCCTGGTGGGCGTAGGGCCCGA AAC A PRXL2B Ensembl:ENSG00000157870 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:2587025..2587222 26863196 MeRIP-seq:(Medium) rs1315792030 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_349788,Human_RBP_ID_4075024,Human_RBP_ID_5413818,Human_RBP_ID_5485928,Human_RBP_ID_22427998 Human_Splice_Rec_8059,Human_Splice_Rec_8071,Human_Splice_Rec_8083,Human_Splice_Rec_8095,Human_Splice_Rec_8105,Human_Splice_Rec_8117,Human_Splice_Rec_8129,Human_Splice_Rec_8139,Human_Splice_Rec_8149,Human_Splice_Rec_8161,Human_Splice_Rec_8171,Human_Splice_Rec_8177,Human_Splice_Rec_8187,Human_Splice_Rec_8197 67098 RMVar_ID_67098 Human_SNP_ID_712130 m1A Human chr1 - 2587224 2587224 2587224 CCAGGGCCTCGGGCCCTACGCCCACCAGGCGCACGCCGTGTTGGTCCAGGAGCCCAGCAAGGCTG CCAGGGCCTCGGGCCCTACGCCCACCAGGCGCCCGCCGTGTTGGTCCAGGAGCCCAGCAAGGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2587034..2587223 26863196 MeRIP-seq:(Medium) rs1258591076 Functional Loss SNV dbSNP153 33..33 33 - - - 67099 RMVar_ID_67099 Human_SNP_ID_712164 m1A Human chr1 + 2587281 2587281 2587281 GGCCCTGGGTCTGCAGGAGTTCCTGGACGGCGACTACTTCGCGGGAGGTGCGTCCTGTTCCCCGC GGCCCTGGGTCTGCAGGAGTTCCTGGACGGCGTCTACTTCGCGGGAGGTGCGTCCTGTTCCCCGC A T PRXL2B Ensembl:ENSG00000157870 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2587088..2587782 32194978 MeRIP-seq:(Medium) rs1224350440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_8059,Human_Splice_Rec_8071,Human_Splice_Rec_8083,Human_Splice_Rec_8095,Human_Splice_Rec_8105,Human_Splice_Rec_8117,Human_Splice_Rec_8129,Human_Splice_Rec_8139,Human_Splice_Rec_8149,Human_Splice_Rec_8161,Human_Splice_Rec_8171,Human_Splice_Rec_8177,Human_Splice_Rec_8187,Human_Splice_Rec_8197 67100 RMVar_ID_67100 Human_SNP_ID_712607 m1A Human chr1 - 2588472 2588472 2588472 CCTGGGAGCTCCCACCACCCCCCGGCCTGTACACCCTTGACCCGCACACACCTTGGCAGCCACAT CCTGGGAGCTCCCACCACCCCCCGGCCTGTACCCCCTTGACCCGCACACACCTTGGCAGCCACAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2588468..2588561 26863196 MeRIP-seq:(Medium) rs764179151 Functional Loss SNV dbSNP153 33..33 33 - - - 67101 RMVar_ID_67101 Human_SNP_ID_947336 m1A Human chr1 - 3325940 3325940 3325940 GGAGGACCAAGGATCGTCGAGGATGGCCAAGGAGGGCCAAGAGGGCCGAGGAGGGCCAAGGAGGG GGAGGACCAAGGATCGTCGAGGATGGCCAAGGGGGGCCAAGAGGGCCGAGGAGGGCCAAGGAGGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:3325897..3326034 26863196 MeRIP-seq:(Medium) rs1282337471 Functional Loss SNV dbSNP153 33..33 33 - - - 67102 RMVar_ID_67102 Human_SNP_ID_987988 m1A Human chr1 - 3463201 3463201 3463201 AAGGCGGCATCGTCTCTAACACGCGGGGAGCCACGGACCATTGGGAGCCCGGAGGCTGGGTTCCC AAGGCGGCATCGTCTCTAACACGCGGGGAGCCGCGGACCATTGGGAGCCCGGAGGCTGGGTTCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3463076..3463226 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 67103 RMVar_ID_67103 Human_SNP_ID_988178 m1A Human chr1 + 3463667 3463667 3463667 CCAGCCAGCCTCATACTCGGAGCCCGGCCAAAAACAAGGTAGGGGCCTGCTCGTGTGGACCGTGG CCAGCCAGCCTCATACTCGGAGCCCGGCCAAACACAAGGTAGGGGCCTGCTCGTGTGGACCGTGG A C ARHGEF16 Ensembl:ENSG00000130762 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3463573..3466055 32194978 MeRIP-seq:(Medium) rs1368328332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518343 Human_Splice_Rec_8651 67104 RMVar_ID_67104 Human_SNP_ID_989960 m1A Human chr1 - 3469503 3469503 3469503 GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCAGGAACTCCTCCACCAGGATGCTCAGGCTGTGC GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCGGGAACTCCTCCACCAGGATGCTCAGGCTGTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3468931..3469527 32194978 MeRIP-seq:(Medium) rs553627615 Functional Loss SNV dbSNP153 33..33 33 - - - 67105 RMVar_ID_67105 Human_SNP_ID_989961 m1A Human chr1 - 3469503 3469503 3469503 GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCAGGAACTCCTCCACCAGGATGCTCAGGCTGTGC GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCCGGAACTCCTCCACCAGGATGCTCAGGCTGTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3468931..3469527 32194978 MeRIP-seq:(Medium) rs553627615 Functional Loss SNV dbSNP153 33..33 33 - - - 67106 RMVar_ID_67106 Human_SNP_ID_990358 m1A Human chr1 - 3470640 3470639 3470641 ACTCACATACATCCCTGACCACGCAGATACACAGACATCCCTGCCCACGCACACACACCCACTCA ACTCACATACATCCCTGACCACGCAGATACA__GACATCCCTGCCCACGCACACACACCCACTCA CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3470350..3470753 26863196 MeRIP-seq:(Medium) rs1382640531 Functional Loss DEL dbSNP153 32..33 33 - - - 67107 RMVar_ID_67107 Human_SNP_ID_990441 m1A Human chr1 - 3470885 3470833 3470885 ACACACATACCCCTGGCCAGGCACACACACCCACGCACATACACCCCTGCCCACGCACACACACC ACACACATACCCCTGGCCAGGCACACACACCC_________________________________ GGGGTGTGTGTGCGTGGACAGGTGTGTGTGCGTGGGCAGGGGTGTATGTGCGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3470881..3471036 26863196 MeRIP-seq:(Medium) rs1557693485 Functional Loss DEL dbSNP153 33..65 33 - - - 67108 RMVar_ID_67108 Human_SNP_ID_990466 m1A Human chr1 - 3470885 3470871 3470885 ACACACATACCCCTGGCCAGGCACACACACCCACGCACATACACCCCTGCCCACGCACACACACC ACACACATACCCCTGGCCAGGCACACACACCC______________CTGCCCACGCACACACACC GGGGTGTATGTGCGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3470881..3471036 26863196 MeRIP-seq:(Medium) rs1382345125 Functional Loss DEL dbSNP153 33..46 33 - - - 67109 RMVar_ID_67109 Human_SNP_ID_992064 m1A Human chr1 - 3476022 3476022 3476022 TGCTGAAGTCCAGCTGTGTGTGCAGCGTGTACATCTGCTCCATGCGCTCCATCCTGTGGGCCCCC TGCTGAAGTCCAGCTGTGTGTGCAGCGTGTACCTCTGCTCCATGCGCTCCATCCTGTGGGCCCCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3474766..3476053 32194978 MeRIP-seq:(Medium) rs1353008582 Functional Loss SNV dbSNP153 33..33 33 - - - 67110 RMVar_ID_67110 Human_SNP_ID_998254 m1A Human chr1 - 3494243 3494243 3494243 AGGTGGGGAGCCAGCAGCAGTGGGGAGGGACGAGGACGGGCAGGAGGGGGCTTTTCTCGGGCCCC AGGTGGGGAGCCAGCAGCAGTGGGGAGGGACGGGGACGGGCAGGAGGGGGCTTTTCTCGGGCCCC T C MEGF6 Ensembl:ENSG00000162591 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3494240..3494348 26863196 MeRIP-seq:(Medium) rs1235125988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22716,RMVar_hsa_circ_128489,RMVar_hsa_circ_78729,RMVar_hsa_circ_95007,RMVar_hsa_circ_374134,RMVar_hsa_circ_128490,RMVar_hsa_circ_128491 67111 RMVar_ID_67111 Human_SNP_ID_1001706 m1A Human chr1 - 3502057 3502052 3502057 GGGGGGCACACTCGCCAGGAGCCCATGTGAGGAGGCGCCGGGGGGGCACACTCGCCAGGAGCCCA GGGGGGCACACTCGCCAGGAGCCCATGTGAGG_____CCGGGGGGGCACACTCGCCAGGAGCCCA GCGCCT G MEGF6 Ensembl:ENSG00000162591 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3502008..3502107 26863196 MeRIP-seq:(Medium) rs1358506112 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_1034,Human_RBP_ID_189618,Human_RBP_ID_258797,Human_RBP_ID_1064238,Human_RBP_ID_3328085,Human_RBP_ID_5086157,Human_RBP_ID_5311485,Human_RBP_ID_5332544,Human_RBP_ID_5642127,Human_RBP_ID_8051591,Human_RBP_ID_8166457,Human_RBP_ID_8227942,Human_RBP_ID_8724630,Human_RBP_ID_8940108,Human_RBP_ID_9411641,Human_RBP_ID_17337921,Human_RBP_ID_17646246,Human_RBP_ID_18409900,Human_RBP_ID_18415329,Human_RBP_ID_18454969,Human_RBP_ID_18473598,Human_RBP_ID_22636074,Human_RBP_ID_22706570,Human_RBP_ID_22734586,Human_RBP_ID_24540928,Human_RBP_ID_26767131,Human_RBP_ID_26772929 RMVar_hsa_circ_95007,RMVar_hsa_circ_374134,RMVar_hsa_circ_24698,RMVar_hsa_circ_126718,RMVar_hsa_circ_128490,RMVar_hsa_circ_128491,RMVar_hsa_circ_128492,RMVar_hsa_circ_33097 67112 RMVar_ID_67112 Human_SNP_ID_1010752 m1A Human chr1 + 3531110 3531110 3531110 ACCTGGCCTCTGGTCACCGGCGCTCACGGGGTAGCCGGCCTGGCCCAGGTGACATGGGTAGCAGC ACCTGGCCTCTGGTCACCGGCGCTCACGGGGTTGCCGGCCTGGCCCAGGTGACATGGGTAGCAGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3531104..3531276 32194978 MeRIP-seq:(Medium) rs1249965915 Functional Loss SNV dbSNP153 33..33 33 - - - 67113 RMVar_ID_67113 Human_SNP_ID_1010860 m1A Human chr1 + 3531323 3531323 3531323 TGCGCCCTAAGCCGGCGGCCGGGCGACGGGGCAGGCGGCTCGGGCTGGTTCTGGGTTCCGGGCGG TGCGCCCTAAGCCGGCGGCCGGGCGACGGGGCCGGCGGCTCGGGCTGGTTCTGGGTTCCGGGCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3531274..3531400 26863196 MeRIP-seq:(Medium) rs1458374771 Functional Loss SNV dbSNP153 33..33 33 - - - 67114 RMVar_ID_67114 Human_SNP_ID_1015329 m1A Human chr1 + 3545984 3545984 3545984 TCCAAACGGCTCGCAGCTGGACAGCTGGAGACAGCGTTGCGTTTGGCAAGGGAAGTTCTGGGAGA TCCAAACGGCTCGCAGCTGGACAGCTGGAGACGGCGTTGCGTTTGGCAAGGGAAGTTCTGGGAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3545977..3546083 26863196 MeRIP-seq:(Medium) rs1362012571 Functional Loss SNV dbSNP153 33..33 33 - - - 67115 RMVar_ID_67115 Human_SNP_ID_1015470 m1A Human chr1 + 3546530 3546527 3546530 TGTGGGCCAGGAAGGAGGGTGCCAGGGAGGGCACCGAGGCGGGGTGGCAGTGGGCTGGGAAGGGG TGTGGGCCAGGAAGGAGGGTGCCAGGGAGG___CCGAGGCGGGGTGGCAGTGGGCTGGGAAGGGG GGCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:3546520..3546738 26863196 MeRIP-seq:(Medium) rs1439307376 Functional Loss DEL dbSNP153 31..33 33 - - - 67116 RMVar_ID_67116 Human_SNP_ID_1015590 m1A Human chr1 - 3546739 3546739 3546739 GCCATGGTGGCCTCCCTGGCACCCTCCTTCCCAGCCCGCTGCCACCCCGCCTTGGCGTCCTCCTT GCCATGGTGGCCTCCCTGGCACCCTCCTTCCCGGCCCGCTGCCACCCCGCCTTGGCGTCCTCCTT T C MEGF6 Ensembl:ENSG00000162591 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3546737..3546978 26863196 MeRIP-seq:(Medium) rs1371126130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070974 RMVar_hsa_circ_95007,RMVar_hsa_circ_126718,RMVar_hsa_circ_128490,RMVar_hsa_circ_128492,RMVar_hsa_circ_120777,RMVar_hsa_circ_128494 67117 RMVar_ID_67117 Human_SNP_ID_1035208 m1A Human chr1 - 3611381 3611381 3611381 CTCCGCACCTGCAGCGACCTTGGGCTCCGCGGAGCGGGCGCGGGCACCTGTGGCTGCGTCCTATG CTCCGCACCTGCAGCGACCTTGGGCTCCGCGGTGCGGGCGCGGGCACCTGTGGCTGCGTCCTATG T A MEGF6 Ensembl:ENSG00000162591 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:3611380..3611483 26863196 MeRIP-seq:(Medium) rs1210222307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120777,RMVar_hsa_circ_128494 67118 RMVar_ID_67118 Human_SNP_ID_1038939 m1A Human chr1 + 3625061 3625061 3625061 CGGTCGCGTCGGCGTCAGGGTCGGGGTCGGTAAGGGGTGCGGCAATGCTGCAACTGCGGGACTCG CGGTCGCGTCGGCGTCAGGGTCGGGGTCGGTAGGGGGTGCGGCAATGCTGCAACTGCGGGACTCG A G TPRG1L Ensembl:ENSG00000158109 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:3625015..3625200 26863196 MeRIP-seq:(Medium) rs28695195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743522,Human_RBP_ID_4072455,Human_RBP_ID_9412380 Human_miRNA_ID_1935792,Human_miRNA_ID_1946892 RMVar_hsa_circ_97705,RMVar_hsa_circ_128500 67119 RMVar_ID_67119 Human_SNP_ID_1038943 m1A Human chr1 + 3625073 3625073 3625073 CGTCAGGGTCGGGGTCGGTAAGGGGTGCGGCAATGCTGCAACTGCGGGACTCGGTGGACTCGGCC CGTCAGGGTCGGGGTCGGTAAGGGGTGCGGCAGTGCTGCAACTGCGGGACTCGGTGGACTCGGCC A G TPRG1L Ensembl:ENSG00000158109 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3624999..3625743 26863196 MeRIP-seq:(Medium) rs1414088994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353306,Human_RBP_ID_743522,Human_RBP_ID_4072455,Human_RBP_ID_9412380 Human_miRNA_ID_1935792,Human_miRNA_ID_1946892 RMVar_hsa_circ_97705,RMVar_hsa_circ_128500 67120 RMVar_ID_67120 Human_SNP_ID_1039249 m1A Human chr1 - 3625683 3625683 3625683 ACCCTGTAGGCAGAGGAGGGGCCTCAGTCCACACTGGACGCGGCTGTCTCGACTTAGCCAAGGCC ACCCTGTAGGCAGAGGAGGGGCCTCAGTCCACCCTGGACGCGGCTGTCTCGACTTAGCCAAGGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3625681..3625774 26863196 MeRIP-seq:(Medium) rs200810867 Functional Loss SNV dbSNP153 33..33 33 - - - 67121 RMVar_ID_67121 Human_SNP_ID_1058719 m1A Human chr1 + 3693745 3693745 3693745 CCCTCCTCCTGCAATCCCAGCCCTGCAGCCTCAGCTCCTCCTCCCACAATCCCACCCATGCAGCC CCCTCCTCCTGCAATCCCAGCCCTGCAGCCTCCGCTCCTCCTCCCACAATCCCACCCATGCAGCC A C TP73 Ensembl:ENSG00000078900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3693743..3693871 26863196 MeRIP-seq:(Medium) rs1487979865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12115 67122 RMVar_ID_67122 Human_SNP_ID_1058720 m1A Human chr1 + 3693745 3693745 3693745 CCCTCCTCCTGCAATCCCAGCCCTGCAGCCTCAGCTCCTCCTCCCACAATCCCACCCATGCAGCC CCCTCCTCCTGCAATCCCAGCCCTGCAGCCTCGGCTCCTCCTCCCACAATCCCACCCATGCAGCC A G TP73 Ensembl:ENSG00000078900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3693743..3693871 26863196 MeRIP-seq:(Medium) rs1487979865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12115 67123 RMVar_ID_67123 Human_SNP_ID_1069210 m1A Human chr1 + 3728203 3728203 3728203 GTGTGAAGAAGCGGCGGCATGGAGACGAGGACACGTACTACCTTCAGGTGAGTGTGTGCTCCTGC GTGTGAAGAAGCGGCGGCATGGAGACGAGGACTCGTACTACCTTCAGGTGAGTGTGTGCTCCTGC A T TP73 Ensembl:ENSG00000078900 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3728152..3729461 32194978 MeRIP-seq:(Medium) rs781299594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_9118,Human_Splice_Rec_9119,Human_Splice_Rec_9144,Human_Splice_Rec_9145,Human_Splice_Rec_9164,Human_Splice_Rec_9165,Human_Splice_Rec_9188,Human_Splice_Rec_9189,Human_Splice_Rec_9210,Human_Splice_Rec_9211,Human_Splice_Rec_9230,Human_Splice_Rec_9231,Human_Splice_Rec_9250,Human_Splice_Rec_9251,Human_Splice_Rec_9268,Human_Splice_Rec_9269,Human_Splice_Rec_9288,Human_Splice_Rec_9289,Human_Splice_Rec_9308,Human_Splice_Rec_9309,Human_Splice_Rec_9330,Human_Splice_Rec_9331,Human_Splice_Rec_9346,Human_Splice_Rec_9347,Human_Splice_Rec_9358,Human_Splice_Rec_9359 67124 RMVar_ID_67124 Human_SNP_ID_1071302 m1A Human chr1 + 3734209 3734207 3734210 TGCTTTCCTTTCTAGGCGGTGGCAGTCAGGGAACAGACTGAGGTAGGTGTAGGGGGGTCTAGGCC TGCTTTCCTTTCTAGGCGGTGGCAGTCAGGG___AGACTGAGGTAGGTGTAGGGGGGTCTAGGCC GAAC G TP73 Ensembl:ENSG00000078900 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3734161..3734262 32194978 MeRIP-seq:(Medium) rs1315577467 Functional Loss DEL dbSNP153 32..34 33 - - - 67125 RMVar_ID_67125 Human_SNP_ID_1072674 m1A Human chr1 - 3739278 3739276 3739278 GTTAGATAGAGGTCATCAGCTGGGTTGATTGTACGGGTTAGATAGAGGTCGTCAGCCGGGTTGAT GTTAGATAGAGGTCATCAGCTGGGTTGATTGT__GGGTTAGATAGAGGTCGTCAGCCGGGTTGAT CGT C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1448264341 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3332641,Human_RBP_ID_5086360,Human_RBP_ID_5233790,Human_RBP_ID_5279329,Human_RBP_ID_5642563,Human_RBP_ID_9410920,Human_RBP_ID_17182597,Human_RBP_ID_17224458,Human_RBP_ID_17580942,Human_RBP_ID_18926158,Human_RBP_ID_22469136,Human_RBP_ID_23263260,Human_RBP_ID_24358392 Human_Splice_Rec_9476 67126 RMVar_ID_67126 Human_SNP_ID_1072678 m1A Human chr1 - 3739278 3739278 3739278 GTTAGATAGAGGTCATCAGCTGGGTTGATTGTACGGGTTAGATAGAGGTCGTCAGCCGGGTTGAT GTTAGATAGAGGTCATCAGCTGGGTTGATTGTGCGGGTTAGATAGAGGTCGTCAGCCGGGTTGAT T C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs973025229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3332641,Human_RBP_ID_5086360,Human_RBP_ID_5233790,Human_RBP_ID_5279329,Human_RBP_ID_5642563,Human_RBP_ID_9410920,Human_RBP_ID_17182597,Human_RBP_ID_17224458,Human_RBP_ID_17580942,Human_RBP_ID_18926158,Human_RBP_ID_22469136,Human_RBP_ID_23263260,Human_RBP_ID_24358392 Human_Splice_Rec_9476 67127 RMVar_ID_67127 Human_SNP_ID_1072697 m1A Human chr1 - 3739314 3739314 3739314 GTTAGATAGAGGTCATCAGCTGGGTTGATTGTATGGGTTAGATAGAGGTCATCAGCTGGGTTGAT GTTAGATAGAGGTCATCAGCTGGGTTGATTGTGTGGGTTAGATAGAGGTCATCAGCTGGGTTGAT T C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:3739208..3739350;chr1:3739144..3739375 26863196 MeRIP-seq:(Medium) rs375473604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353968,Human_RBP_ID_3332641,Human_RBP_ID_5086360,Human_RBP_ID_8171225,Human_RBP_ID_9412744,Human_RBP_ID_22369495,Human_RBP_ID_23263260,Human_RBP_ID_23391778,Human_RBP_ID_24358392 Human_Splice_Rec_9468,Human_Splice_Rec_9476 67128 RMVar_ID_67128 Human_SNP_ID_1072766 m1A Human chr1 - 3739555 3739484 3739556 GTCGTCAGCCGGGTTGATTGTGTGGGTTAGACAGAGGTCATCAGCTGGGTTGATTCTGCGGGTTA GTCGTCAGCCGGGTTGATTGTGTGGGTTAGA__________________________________ ATCTAACCCACACAATCAACCCAGCTGATGACCTCTATCTAACCCGCAGAATCAACCCAGCTGATGACCTCTG A TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3739426..3740327 26863196 MeRIP-seq:(Medium) rs1557608071 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_801648,Human_RBP_ID_5332546,Human_RBP_ID_9412745,Human_RBP_ID_17204367,Human_RBP_ID_18930613,Human_RBP_ID_23391785 67129 RMVar_ID_67129 Human_SNP_ID_1072816 m1A Human chr1 - 3739636 3739636 3739636 TAGATAGAGATCATCAGCTGGGTTGATTCTGCAGGTTAGATAGAGGTCATCAGCTGGGTTGACTA TAGATAGAGATCATCAGCTGGGTTGATTCTGCGGGTTAGATAGAGGTCATCAGCTGGGTTGACTA T C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs368215129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8242616,Human_RBP_ID_9552963,Human_RBP_ID_10481916,Human_RBP_ID_10965371,Human_RBP_ID_17182598,Human_RBP_ID_18524351,Human_RBP_ID_23391789 Human_Splice_Rec_9521 67130 RMVar_ID_67130 Human_SNP_ID_1072991 m1A Human chr1 + 3740065 3740065 3740065 AATCAACCTGGCTGATGACCTCTATCTAACCCACACAATCTACCAGGCTGATGATCTCTATCTAA AATCAACCTGGCTGATGACCTCTATCTAACCCGCACAATCTACCAGGCTGATGATCTCTATCTAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:3739930..3740205 26863196 MeRIP-seq:(Medium) rs1407635649 Functional Loss SNV dbSNP153 33..33 33 - - - 67131 RMVar_ID_67131 Human_SNP_ID_1074715 m1A Human chr1 - 3746083 3746083 3746083 CTCAGCCTCAGCTCATTCTCTCAGGCAGTCCCAGCATTGGCACGGTACCTCCTCCCGCTGTGGGC CTCAGCCTCAGCTCATTCTCTCAGGCAGTCCCGGCATTGGCACGGTACCTCCTCCCGCTGTGGGC T C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3746034..3746175 26863196 MeRIP-seq:(Medium) rs367658674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17218317,Human_RBP_ID_17456737,Human_RBP_ID_18186770 Human_Splice_Rec_9386 RMVar_hsa_circ_282232,RMVar_hsa_circ_349368,RMVar_hsa_circ_10692 67132 RMVar_ID_67132 Human_SNP_ID_1074721 m1A Human chr1 + 3746097 3746093 3746097 GAGGTACCGTGCCAATGCTGGGACTGCCTGAGAGAATGAGCTGAGGCTGAGGCTGACGGGGCAAG GAGGTACCGTGCCAATGCTGGGACTGCCT____GAATGAGCTGAGGCTGAGGCTGACGGGGCAAG TGAGA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3746049..3746141 26863196 MeRIP-seq:(Medium) rs753427645 Functional Loss DEL dbSNP153 30..33 33 - - - 67133 RMVar_ID_67133 Human_SNP_ID_1074722 m1A Human chr1 + 3746097 3746093 3746097 GAGGTACCGTGCCAATGCTGGGACTGCCTGAGAGAATGAGCTGAGGCTGAGGCTGACGGGGCAAG GAGGTACCGTGCCAATGCTGGGACTGCCTGA__GAATGAGCTGAGGCTGAGGCTGACGGGGCAAG TGAGA TGA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3746049..3746141 26863196 MeRIP-seq:(Medium) rs753427645 Functional Loss DEL dbSNP153 32..33 33 - - - 67134 RMVar_ID_67134 Human_SNP_ID_1082969 m1A Human chr1 + 3773171 3773171 3773171 CAACCTGGCCCAGAGGCCCCAGCCCTCAGGCAAGGTTCTCCGGGTAAGTGTGGGGCCCTGAGGCG CAACCTGGCCCAGAGGCCCCAGCCCTCAGGCAGGGTTCTCCGGGTAAGTGTGGGGCCCTGAGGCG A G SMIM1 Ensembl:ENSG00000235169 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3773121..3775429 26863196 MeRIP-seq:(Medium) rs1304773568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073460,Human_RBP_ID_19033731 Human_Splice_Rec_9651,Human_Splice_Rec_9657,Human_Splice_Rec_9661,Human_Splice_Rec_9665 RMVar_hsa_circ_82149,RMVar_hsa_circ_128512 67135 RMVar_ID_67135 Human_SNP_ID_1086300 m1A Human chr1 - 3784074 3784074 3784074 CCCCTTGGGGCGGAAAGAAGCCAAGGCCAAGGAGCTGGTGCGGCAGCTGCAGCTGGAGGCCGAGG CCCCTTGGGGCGGAAAGAAGCCAAGGCCAAGGTGCTGGTGCGGCAGCTGCAGCTGGAGGCCGAGG T A LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3784026..3784075 26863196 MeRIP-seq:(Medium) rs775529048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5336751,Human_RBP_ID_9355391,Human_RBP_ID_17750277,Human_RBP_ID_18966979,Human_RBP_ID_24747849,Human_RBP_ID_26310093 Human_Splice_Rec_9672,Human_Splice_Rec_9673,Human_Splice_Rec_9679,Human_Splice_Rec_9685 RMVar_hsa_circ_69235,RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_118247,RMVar_hsa_circ_87388,RMVar_hsa_circ_128516,RMVar_hsa_circ_128514,RMVar_hsa_circ_327213,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889,RMVar_hsa_circ_357951 67136 RMVar_ID_67136 Human_SNP_ID_1086638 m1A Human chr1 - 3785088 3785088 3785088 GCTGTACTGCGCCCGGCCCCCACAGGACCTCAAGGTGCTGCAGCCTCCTTTGCAGGGTCTGCTGA GCTGTACTGCGCCCGGCCCCCACAGGACCTCAGGGTGCTGCAGCCTCCTTTGCAGGGTCTGCTGA T C LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs752248261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19036457,Human_RBP_ID_22022631,Human_RBP_ID_26797534 Human_Splice_Rec_9671 RMVar_hsa_circ_69235,RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_87388,RMVar_hsa_circ_128514,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889 67137 RMVar_ID_67137 Human_SNP_ID_1087329 m1A Human chr1 - 3787099 3787099 3787099 CGGGAAGGGCAAGGGCCGTGCCGAGGGCTCGGAGAAGGAAGAGAGCCGGAGGAAGAGGAGGGAGA CGGGAAGGGCAAGGGCCGTGCCGAGGGCTCGGGGAAGGAAGAGAGCCGGAGGAAGAGGAGGGAGA T C LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:3787051..3787201 26863196 MeRIP-seq:(Medium) rs779423452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742622,Human_RBP_ID_3932558,Human_RBP_ID_18964556,Human_RBP_ID_22022633,Human_RBP_ID_26313227 RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_87388,RMVar_hsa_circ_128514,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889 67138 RMVar_ID_67138 Human_SNP_ID_1089976 m1A Human chr1 - 3796001 3796001 3796001 GGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCAACCTCACCGGCAATTGCCTAGACTCCTTTCCCG GGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCATCCTCACCGGCAATTGCCTAGACTCCTTTCCCG T A LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3795851..3796125 26863196 MeRIP-seq:(Medium) rs1053796921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1430857,Human_RBP_ID_4049529,Human_RBP_ID_8753430,Human_RBP_ID_9268677,Human_RBP_ID_18573946 Human_miRNA_ID_2006094 RMVar_hsa_circ_123853,RMVar_hsa_circ_128514 67139 RMVar_ID_67139 Human_SNP_ID_1089977 m1A Human chr1 - 3796001 3796001 3796001 GGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCAACCTCACCGGCAATTGCCTAGACTCCTTTCCCG GGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCAGCCTCACCGGCAATTGCCTAGACTCCTTTCCCG T C LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:3795851..3796125 26863196 MeRIP-seq:(Medium) rs1053796921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1430857,Human_RBP_ID_4049529,Human_RBP_ID_8753430,Human_RBP_ID_9268677,Human_RBP_ID_18573946 Human_miRNA_ID_2006094 RMVar_hsa_circ_123853,RMVar_hsa_circ_128514 67140 RMVar_ID_67140 Human_SNP_ID_1089978 m1A Human chr1 - 3796002 3796002 3796002 TGGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCAACCTCACCGGCAATTGCCTAGACTCCTTTCCC TGGCGCGCTGCGCCCCGCGCCTGCAGAGCCTCGACCTCACCGGCAATTGCCTAGACTCCTTTCCC T C LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:3795901..3796150 26863410 MeRIP-seq:(Medium) rs1332864611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1430857,Human_RBP_ID_8753430,Human_RBP_ID_9268677,Human_RBP_ID_18573946 Human_miRNA_ID_2006094 RMVar_hsa_circ_123853,RMVar_hsa_circ_128514 67141 RMVar_ID_67141 Human_SNP_ID_1089994 m1A Human chr1 + 3796026 3796026 3796026 GGTGAGGTTGAGGCTCTGCAGGCGCGGGGCGCAGCGCGCCAGGTCGGCTGGCAGCTCGCGCAGCC GGTGAGGTTGAGGCTCTGCAGGCGCGGGGCGCCGCGCGCCAGGTCGGCTGGCAGCTCGCGCAGCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,untreat control chr1:3795990..3796225;chr1:3795957..3796057 26863196,26863410 MeRIP-seq:(Medium) rs913878056 Functional Loss SNV dbSNP153 33..33 33 - - - 67142 RMVar_ID_67142 Human_SNP_ID_1089995 m1A Human chr1 + 3796026 3796026 3796026 GGTGAGGTTGAGGCTCTGCAGGCGCGGGGCGCAGCGCGCCAGGTCGGCTGGCAGCTCGCGCAGCC GGTGAGGTTGAGGCTCTGCAGGCGCGGGGCGCTGCGCGCCAGGTCGGCTGGCAGCTCGCGCAGCC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,untreat control chr1:3795990..3796225;chr1:3795957..3796057 26863196,26863410 MeRIP-seq:(Medium) rs913878056 Functional Loss SNV dbSNP153 33..33 33 - - - 67143 RMVar_ID_67143 Human_SNP_ID_1090007 m1A Human chr1 - 3796042 3796042 3796042 AACCTCAGCGGCAACCGGCTGCGCGAGCTGCCAGCCGACCTGGCGCGCTGCGCCCCGCGCCTGCA AACCTCAGCGGCAACCGGCTGCGCGAGCTGCCGGCCGACCTGGCGCGCTGCGCCCCGCGCCTGCA T C LRRC47 Ensembl:ENSG00000130764 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:3795993..3796135 26863196 MeRIP-seq:(Medium) rs950968092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8753430,Human_RBP_ID_9270822 RMVar_hsa_circ_123853,RMVar_hsa_circ_128514 67144 RMVar_ID_67144 Human_SNP_ID_1090175 m1A Human chr1 + 3796450 3796450 3796450 CGCTCGCGCTCAGCCAGCTCCAGCTCCGGCCAAGACTCTGACACCGCTGCCGCCGCCATGGCGCC CGCTCGCGCTCAGCCAGCTCCAGCTCCGGCCAGGACTCTGACACCGCTGCCGCCGCCATGGCGCC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:3796354..3796504 26863410 MeRIP-seq:(Medium) rs1191892446 Functional Loss SNV dbSNP153 33..33 33 - - - 67145 RMVar_ID_67145 Human_SNP_ID_1090182 m1A Human chr1 + 3796458 3796458 3796458 CTCAGCCAGCTCCAGCTCCGGCCAAGACTCTGACACCGCTGCCGCCGCCATGGCGCCTCAGCTGC CTCAGCCAGCTCCAGCTCCGGCCAAGACTCTGTCACCGCTGCCGCCGCCATGGCGCCTCAGCTGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:3796295..3796525;chr1:3796293..3796525 26863196 MeRIP-seq:(Medium) rs923960813 Functional Loss SNV dbSNP153 33..33 33 - - - 67146 RMVar_ID_67146 Human_SNP_ID_1096136 m1A Human chr1 - 3818204 3818204 3818204 GTAGACAGAGGAGAAGCCCCAGGCAGAGTGGGAGGAAGAAGGCAAACCAGGCGCTGGGGAAGAAA GTAGACAGAGGAGAAGCCCCAGGCAGAGTGGGTGGAAGAAGGCAAACCAGGCGCTGGGGAAGAAA T A CEP104 Ensembl:ENSG00000116198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3818179..3818378 26863196 MeRIP-seq:(Medium) rs1288259990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109312,RMVar_hsa_circ_128519 67147 RMVar_ID_67147 Human_SNP_ID_1106978 m1A Human chr1 - 3857562 3857562 3857562 CCTCAAGCCCTCTGGGTCCCACAGGCGGTGGCACCTGCTGCCCAGCTGCTCAGATCCGTCCTCGC CCTCAAGCCCTCTGGGTCCCACAGGCGGTGGCGCCTGCTGCCCAGCTGCTCAGATCCGTCCTCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3857512..3857593 26863196 MeRIP-seq:(Medium) rs754398581 Functional Loss SNV dbSNP153 33..33 33 - - - 67148 RMVar_ID_67148 Human_SNP_ID_1106979 m1A Human chr1 - 3857562 3857562 3857562 CCTCAAGCCCTCTGGGTCCCACAGGCGGTGGCACCTGCTGCCCAGCTGCTCAGATCCGTCCTCGC CCTCAAGCCCTCTGGGTCCCACAGGCGGTGGCCCCTGCTGCCCAGCTGCTCAGATCCGTCCTCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3857512..3857593 26863196 MeRIP-seq:(Medium) rs754398581 Functional Loss SNV dbSNP153 33..33 33 - - - 67149 RMVar_ID_67149 Human_SNP_ID_1116570 m1A Human chr1 + 3891688 3891688 3891688 CGATGGCTGGGCTAGGGTGAACGGCAGACGGCATGAGATTCCTTTCCCCACCCACTCTGCCTTTC CGATGGCTGGGCTAGGGTGAACGGCAGACGGCCTGAGATTCCTTTCCCCACCCACTCTGCCTTTC A C LINC01134 RNACentral:URS00008B8DF5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:3891683..3891762 26863196 MeRIP-seq:(Medium) rs992821858 Functional Loss SNV dbSNP153 33..33 33 - - - 67150 RMVar_ID_67150 Human_SNP_ID_1118929 m1A Human chr1 + 3900210 3900210 3900210 GCTCCTCATGAGTGTGAGCACCGCAGCCAAGCACCGCGCGCCCCGGCCAACGCGTCCCGGCGGAG GCTCCTCATGAGTGTGAGCACCGCAGCCAAGCGCCGCGCGCCCCGGCCAACGCGTCCCGGCGGAG A G LINC01134 RNACentral:URS00008B8DF5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:3900120..3900234;chr1:3900121..3900239;chr1:3900056..3900213 26863196 MeRIP-seq:(Medium) rs776416588 Functional Loss SNV dbSNP153 33..33 33 - - - 67151 RMVar_ID_67151 Human_SNP_ID_1239170 m1A Human chr1 + 4336718 4336718 4336718 TGATGGTGGTGATGGGGGTGATGATGATGGTGATAGTGATGGTGATGATGATGGTGATGGTGGTG TGATGGTGGTGATGGGGGTGATGATGATGGTGGTAGTGATGGTGATGATGATGGTGATGGTGGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:4336675..4336796 26863196 MeRIP-seq:(Medium) rs373571105 Functional Loss SNV dbSNP153 33..33 33 - - - 67152 RMVar_ID_67152 Human_SNP_ID_1461413 m1A Human chr1 + 5160191 5160188 5160192 TCACATGCACTCATACTAACACATACACATACACACAAACACATACACACATACTAACACATACA TCACATGCACTCATACTAACACATACACAT____ACAAACACATACACACATACTAACACATACA TACAC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:5160182..5160329 26863196 MeRIP-seq:(Medium) rs1443206376 Functional Loss DEL dbSNP153 31..34 33 - - - 67153 RMVar_ID_67153 Human_SNP_ID_1638464 m1A Human chr1 + 5813661 5813620 5813662 AGAGGAGGAGGAGGAGGACGAGGAGGATGAGGACGAGGACGAGGAGGAGGAGGAGGAGGATGAGG __________________________________GAGGACGAGGAGGAGGAGGAGGAGGATGAGG GGAGGAGGAAGAGGAGGAGGAGGAGGACGAGGAGGATGAGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5813613..5813711 26863196 MeRIP-seq:(Medium) rs1557551864 Functional Loss DEL dbSNP153 1..34 33 - - - 67154 RMVar_ID_67154 Human_SNP_ID_1638466 m1A Human chr1 + 5813661 5813623 5813662 AGAGGAGGAGGAGGAGGACGAGGAGGATGAGGACGAGGACGAGGAGGAGGAGGAGGAGGATGAGG __________________________________GAGGACGAGGAGGAGGAGGAGGAGGATGAGG GGAGGAAGAGGAGGAGGAGGAGGACGAGGAGGATGAGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5813613..5813711 26863196 MeRIP-seq:(Medium) rs1203483307 Functional Loss DEL dbSNP153 1..34 33 - - - 67155 RMVar_ID_67155 Human_SNP_ID_1638500 m1A Human chr1 + 5813661 5813656 5813662 AGAGGAGGAGGAGGAGGACGAGGAGGATGAGGACGAGGACGAGGAGGAGGAGGAGGAGGATGAGG AGAGGAGGAGGAGGAGGACGAGGAGGAT______GAGGACGAGGAGGAGGAGGAGGAGGATGAGG TGAGGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5813613..5813711 26863196 MeRIP-seq:(Medium) rs1202042082 Functional Loss DEL dbSNP153 29..34 33 - - - 67156 RMVar_ID_67156 Human_SNP_ID_1638502 m1A Human chr1 + 5813661 5813657 5813662 AGAGGAGGAGGAGGAGGACGAGGAGGATGAGGACGAGGACGAGGAGGAGGAGGAGGAGGATGAGG AGAGGAGGAGGAGGAGGACGAGGAGGATG_____GAGGACGAGGAGGAGGAGGAGGAGGATGAGG GAGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5813613..5813711 26863196 MeRIP-seq:(Medium) rs1414862503 Functional Loss DEL dbSNP153 30..34 33 - - - 67157 RMVar_ID_67157 Human_SNP_ID_1638503 m1A Human chr1 + 5813661 5813659 5813662 AGAGGAGGAGGAGGAGGACGAGGAGGATGAGGACGAGGACGAGGAGGAGGAGGAGGAGGATGAGG AGAGGAGGAGGAGGAGGACGAGGAGGATGAG___GAGGACGAGGAGGAGGAGGAGGAGGATGAGG GGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5813613..5813711 26863196 MeRIP-seq:(Medium) rs1488692029 Functional Loss DEL dbSNP153 32..34 33 - - - 67158 RMVar_ID_67158 Human_SNP_ID_1648936 m1A Human chr1 + 5850274 5850274 5850274 GCTCTCTCAGATCATCCACTGGTTAAAAGTAAAAGACAGCTGAACCCTCATGGGGCCATTCATAC GCTCTCTCAGATCATCCACTGGTTAAAAGTAAGAGACAGCTGAACCCTCATGGGGCCATTCATAC A G lnc-KCNAB2-3 RNACentral:URS00008BF5BB lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:5850266..5850351 26863410 MeRIP-seq:(Medium) rs993218134 Functional Loss SNV dbSNP153 33..33 33 - - - 67159 RMVar_ID_67159 Human_SNP_ID_1648945 m1A Human chr1 + 5850305 5850305 5850305 AAAGACAGCTGAACCCTCATGGGGCCATTCATACAAGTCCCTATTTAAGGAACAAGTGATTATGC AAAGACAGCTGAACCCTCATGGGGCCATTCATTCAAGTCCCTATTTAAGGAACAAGTGATTATGC A T lnc-KCNAB2-3 RNACentral:URS00008BF5BB lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:5850251..5850454;chr1:5850251..5850489;chr1:5850256..5850453 26863196 MeRIP-seq:(Medium) rs1323881978 Functional Loss SNV dbSNP153 33..33 33 - - - 67160 RMVar_ID_67160 Human_SNP_ID_1654753 m1A Human chr1 + 5868820 5868813 5868821 CAATGCACACATACATGCACACACATCCACCCACACATGCACACACGCACCCACACACGCATGCA CAATGCACACATACATGCACACACAT________ACATGCACACACGCACCCACACACGCATGCA TCCACCCAC T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:5868796..5868909 26863196 MeRIP-seq:(Medium) rs200441841 Functional Loss DEL dbSNP153 27..34 33 - - - 67161 RMVar_ID_67161 Human_SNP_ID_1654757 m1A Human chr1 + 5868820 5868818 5868820 CAATGCACACATACATGCACACACATCCACCCACACATGCACACACGCACCCACACACGCATGCA CAATGCACACATACATGCACACACATCCACC__CACATGCACACACGCACCCACACACGCATGCA CCA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:5868796..5868909 26863196 MeRIP-seq:(Medium) rs572026887 Functional Loss DEL dbSNP153 32..33 33 - - - 67162 RMVar_ID_67162 Human_SNP_ID_1660055 m1A Human chr1 + 5884956 5884956 5884956 ACTCGACAACCAAGATCACTGCCCAAGCTCCCAGCCGAACCCGTCCTACTCCACAACCAAGATCA ACTCGACAACCAAGATCACTGCCCAAGCTCCCTGCCGAACCCGTCCTACTCCACAACCAAGATCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:5884687..5885345;chr1:5884678..5885356 26863196 MeRIP-seq:(Medium) rs1890188 Functional Loss SNV dbSNP153 33..33 33 - - - 67163 RMVar_ID_67163 Human_SNP_ID_1685807 m1A Human chr1 - 5979978 5979978 5979978 GGACTCCTGGGGTGTGTGAGCCAGACAGAGGTAGTGGGGCATGTGGTCTCTGGACGGGTTGGTTT GGACTCCTGGGGTGTGTGAGCCAGACAGAGGTGGTGGGGCATGTGGTCTCTGGACGGGTTGGTTT T C NPHP4 Ensembl:ENSG00000131697 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:5979973..5980117 26863196 MeRIP-seq:(Medium) rs1040756890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128546,RMVar_hsa_circ_98643,RMVar_hsa_circ_46005,RMVar_hsa_circ_1067,RMVar_hsa_circ_358928,RMVar_hsa_circ_128553,RMVar_hsa_circ_320690,RMVar_hsa_circ_128554,RMVar_hsa_circ_279961,RMVar_hsa_circ_282719,RMVar_hsa_circ_126530,RMVar_hsa_circ_128561,RMVar_hsa_circ_60922,RMVar_hsa_circ_128565,RMVar_hsa_circ_290577,RMVar_hsa_circ_94927,RMVar_hsa_circ_128576,RMVar_hsa_circ_128577,RMVar_hsa_circ_109076,RMVar_hsa_circ_345547,RMVar_hsa_circ_128578,RMVar_hsa_circ_128581,RMVar_hsa_circ_295776,RMVar_hsa_circ_128582,RMVar_hsa_circ_347914,RMVar_hsa_circ_339963,RMVar_hsa_circ_296095,RMVar_hsa_circ_128587,RMVar_hsa_circ_128588 67164 RMVar_ID_67164 Human_SNP_ID_1688872 m1A Human chr1 + 5991808 5991808 5991808 GGGGCGGGGAGGAGGGGCGGAGGGGCGCGGCCAGGCGGGGTCCGCGGACTCCGGCCTGGGAAGGA GGGGCGGGGAGGAGGGGCGGAGGGGCGCGGCCCGGCGGGGTCCGCGGACTCCGGCCTGGGAAGGA A C KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:5991803..5991929 26863196 MeRIP-seq:(Medium) rs539646204 Functional Loss SNV dbSNP153 33..33 33 - - - 67165 RMVar_ID_67165 Human_SNP_ID_1689289 m1A Human chr1 + 5992787 5992787 5992787 CGCGGGGCACAGGATCCGGAGCTGGAGCCCCCAGGTGAGTACCGGGGAGACCCCGGCGGGGCGCG CGCGGGGCACAGGATCCGGAGCTGGAGCCCCCCGGTGAGTACCGGGGAGACCCCGGCGGGGCGCG A C KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:5992738..5992822 26863196 MeRIP-seq:(Medium) rs902794054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853579,Human_RBP_ID_9318523,Human_RBP_ID_18415375,Human_RBP_ID_26310105 Human_Splice_Rec_10551,Human_Splice_Rec_10581,Human_Splice_Rec_10609,Human_Splice_Rec_10641,Human_Splice_Rec_10653,Human_Splice_Rec_10665,Human_Splice_Rec_10667,Human_Splice_Rec_10673,Human_Splice_Rec_10677,Human_Splice_Rec_10693,Human_Splice_Rec_10701,Human_Splice_Rec_10719,Human_Splice_Rec_10749,Human_Splice_Rec_10767,Human_Splice_Rec_10771,Human_Splice_Rec_10795,Human_Splice_Rec_10827 67166 RMVar_ID_67166 Human_SNP_ID_1689290 m1A Human chr1 + 5992787 5992787 5992787 CGCGGGGCACAGGATCCGGAGCTGGAGCCCCCAGGTGAGTACCGGGGAGACCCCGGCGGGGCGCG CGCGGGGCACAGGATCCGGAGCTGGAGCCCCCTGGTGAGTACCGGGGAGACCCCGGCGGGGCGCG A T KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:5992738..5992822 26863196 MeRIP-seq:(Medium) rs902794054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853579,Human_RBP_ID_9318523,Human_RBP_ID_18415375,Human_RBP_ID_26310105 Human_Splice_Rec_10551,Human_Splice_Rec_10581,Human_Splice_Rec_10609,Human_Splice_Rec_10641,Human_Splice_Rec_10653,Human_Splice_Rec_10665,Human_Splice_Rec_10667,Human_Splice_Rec_10673,Human_Splice_Rec_10677,Human_Splice_Rec_10693,Human_Splice_Rec_10701,Human_Splice_Rec_10719,Human_Splice_Rec_10749,Human_Splice_Rec_10767,Human_Splice_Rec_10771,Human_Splice_Rec_10795,Human_Splice_Rec_10827 67167 RMVar_ID_67167 Human_SNP_ID_1693157 m1A Human chr1 + 6005511 6005511 6005511 CAGCTGAGGGCCTTGGAGCACACCTGGTAGGAAGCCAGCCTGTGGACCTGGAGCCGACTGAGGGT CAGCTGAGGGCCTTGGAGCACACCTGGTAGGACGCCAGCCTGTGGACCTGGAGCCGACTGAGGGT A C KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6005507..6005781 26863196 MeRIP-seq:(Medium) rs1485159936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9410934 67168 RMVar_ID_67168 Human_SNP_ID_1695572 m1A Human chr1 + 6011546 6011546 6011546 GGCAGAGGGGGTTGAAGGATGGAAAGGTAGACAGGAGAGGCTGTGAATGGCTCTGGATGCCGAGC GGCAGAGGGGGTTGAAGGATGGAAAGGTAGACGGGAGAGGCTGTGAATGGCTCTGGATGCCGAGC A G KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:6011366..6011550 26863196 MeRIP-seq:(Medium) rs1266717305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258878,Human_RBP_ID_9410936,Human_RBP_ID_22706575 67169 RMVar_ID_67169 Human_SNP_ID_1695930 m1A Human chr1 - 6012634 6012634 6012634 CCTTCATCACCTCCACCACAACCTCCATCTCCACCTCCACCCACCACCTCCGCCTTCATCACCTC CCTTCATCACCTCCACCACAACCTCCATCTCCCCCTCCACCCACCACCTCCGCCTTCATCACCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6012632..6012857 26863196 MeRIP-seq:(Medium) rs1175418994 Functional Loss SNV dbSNP153 33..33 33 - - - 67170 RMVar_ID_67170 Human_SNP_ID_1697579 m1A Human chr1 - 6018619 6018619 6018619 GTCCTGTCGTGAGGCCTCTATCCCAAAATAAAAAAAATTAGCTGGGCGTCGTGGTGCATACCTGT GTCCTGTCGTGAGGCCTCTATCCCAAAATAAACAAAATTAGCTGGGCGTCGTGGTGCATACCTGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6018617..6018786 26863196 MeRIP-seq:(Medium) rs1557935670 Functional Loss SNV dbSNP153 33..33 33 - - - 67171 RMVar_ID_67171 Human_SNP_ID_1699466 m1A Human chr1 + 6026011 6026011 6026011 ACACTGCTGGCAGCAGTGAGGGGAGCTCTTCAACATCACCAGAACCCTCTGCCCTGAGAAAGGGG ACACTGCTGGCAGCAGTGAGGGGAGCTCTTCAGCATCACCAGAACCCTCTGCCCTGAGAAAGGGG A G KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:6025999..6026126 26863196 MeRIP-seq:(Medium) rs80313586 Functional Loss SNV dbSNP153 33..33 33 - - - 67172 RMVar_ID_67172 Human_SNP_ID_1701977 m1A Human chr1 - 6035410 6035410 6035410 TGCTCCTCACAGCATTCCCTGCGCCCACCTCCACCCCCGCCGGCAGACTCTACGCGGCCAGGGTG TGCTCCTCACAGCATTCCCTGCGCCCACCTCCCCCCCCGCCGGCAGACTCTACGCGGCCAGGGTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6035404..6035599 26863196 MeRIP-seq:(Medium) rs964213504 Functional Loss SNV dbSNP153 33..33 33 - - - 67173 RMVar_ID_67173 Human_SNP_ID_1702017 m1A Human chr1 + 6035551 6035551 6035551 ATGTGGGAGGCGGGACGTGGGAGGAAGGGAGGAGTCGGGGTGACTCCCGGGAGTGGGACTGACAC ATGTGGGAGGCGGGACGTGGGAGGAAGGGAGGCGTCGGGGTGACTCCCGGGAGTGGGACTGACAC A C KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6035546..6035697 26863196 MeRIP-seq:(Medium) rs970889081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22706580 67174 RMVar_ID_67174 Human_SNP_ID_1703366 m1A Human chr1 - 6040566 6040566 6040566 CGGGGAGCCCGTCGTTGATTCTGGATACATGGAGCCAGCCTCACTTATCCAGACTTGCTCGGTTT CGGGGAGCCCGTCGTTGATTCTGGATACATGGGGCCAGCCTCACTTATCCAGACTTGCTCGGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6040475..6040580 26863196 MeRIP-seq:(Medium) rs1179462427 Functional Loss SNV dbSNP153 33..33 33 - - - 67175 RMVar_ID_67175 Human_SNP_ID_1718795 m1A Human chr1 + 6097833 6097833 6097833 GGGGCAGATCCTGAGAGGCACGAAACACCTCCAGGGACTTCTGAGTGAGACGGGAGCCGTGGCAA GGGGCAGATCCTGAGAGGCACGAAACACCTCCCGGGACTTCTGAGTGAGACGGGAGCCGTGGCAA A C KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6097823..6097888 26863196 MeRIP-seq:(Medium) rs79733869 Functional Loss SNV dbSNP153 33..33 33 - - - 67176 RMVar_ID_67176 Human_SNP_ID_1719053 m1A Human chr1 - 6098664 6098664 6098664 CACAGTGTGGTGTTTTCTCTTGGATGCAAACCACACTCTTCACTTGGCTTCAAAACAGCTTAAGC CACAGTGTGGTGTTTTCTCTTGGATGCAAACCGCACTCTTCACTTGGCTTCAAAACAGCTTAAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6098614..6098703 26863196 MeRIP-seq:(Medium) rs1477533644 Functional Loss SNV dbSNP153 33..33 33 - - - 67177 RMVar_ID_67177 Human_SNP_ID_1735997 m1A Human chr1 + 6154691 6154691 6154691 CCTTTGCCCTCCTTGGTCTTGGCCTTGCGGATAGGCACAGGCTGGGGCACCTGCGGGGGGCTGAC CCTTTGCCCTCCTTGGTCTTGGCCTTGCGGATGGGCACAGGCTGGGGCACCTGCGGGGGGCTGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6149256..6155655 32194978 MeRIP-seq:(Medium) rs1288553000 Functional Loss SNV dbSNP153 33..33 33 - - - 67178 RMVar_ID_67178 Human_SNP_ID_1748331 m1A Human chr1 + 6197743 6197741 6197744 TCAGAACTTGCTTCTTTTTTTTGCCCCCCTTCACCACAAGCTTTTTCTAAGAAAATACACAAATG TCAGAACTTGCTTCTTTTTTTTGCCCCCCTT___CACAAGCTTTTTCTAAGAAAATACACAAATG TCAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6197651..6197775 26863196 MeRIP-seq:(Medium) rs764243959 Functional Loss DEL dbSNP153 32..34 33 - - - 67179 RMVar_ID_67179 Human_SNP_ID_1748739 m1A Human chr1 - 6199216 6199214 6199217 CCTGATTACCTGGGTGGAGGGCGGGGAAGAAGAACGGGACCTGCTACCCTGGGGAGCCGCGCATT CCTGATTACCTGGGTGGAGGGCGGGGAAGAA___CGGGACCTGCTACCCTGGGGAGCCGCGCATT GTTC G RPL22 Ensembl:ENSG00000116251 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6199212..6199600 26863196 MeRIP-seq:(Medium) rs1318926596 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_800687,Human_RBP_ID_3328100,Human_RBP_ID_5311497,Human_RBP_ID_5336766,Human_RBP_ID_11062499,Human_RBP_ID_17099038,Human_RBP_ID_18473621,Human_RBP_ID_22735359,Human_RBP_ID_23255265,Human_RBP_ID_23406200 RMVar_hsa_circ_29294,RMVar_hsa_circ_337176 67180 RMVar_ID_67180 Human_SNP_ID_1750665 m1A Human chr1 + 6206109 6206109 6206109 ATTCCGAGGGTGGGAGTGAGGAGAGGTAGGAGAGGCCACGGCAGAGGGAGGCCCCGCGCAGAGTG ATTCCGAGGGTGGGAGTGAGGAGAGGTAGGAGTGGCCACGGCAGAGGGAGGCCCCGCGCAGAGTG A T RNF207 Ensembl:ENSG00000158286 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6206073..6206197 26863196 MeRIP-seq:(Medium) rs1210883969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18414836 67181 RMVar_ID_67181 Human_SNP_ID_1750686 m1A Human chr1 + 6206167 6206167 6206167 CAGAGTGGGAACCATCGCCCGGTGCGGGCCTGAACTTCCAGGGCCGGCTACTCCTCGGCAGAGCG CAGAGTGGGAACCATCGCCCGGTGCGGGCCTGCACTTCCAGGGCCGGCTACTCCTCGGCAGAGCG A C RNF207 Ensembl:ENSG00000158286 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6205989..6206245 26863196 MeRIP-seq:(Medium) rs1022952316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18414837 67182 RMVar_ID_67182 Human_SNP_ID_1751134 m1A Human chr1 + 6207468 6207468 6207468 GTTCCTGGTGGACAGCTCAGGGGATGGCGTGGAGGCGGTGCGCTGTGCCAACTGTGACCTGGAGT GTTCCTGGTGGACAGCTCAGGGGATGGCGTGGTGGCGGTGCGCTGTGCCAACTGTGACCTGGAGT A T RNF207 Ensembl:ENSG00000158286 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6207420..6207536 26863196 MeRIP-seq:(Medium) rs1180912584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745242 Human_Splice_Rec_11676,Human_Splice_Rec_11680,Human_Splice_Rec_11712 67183 RMVar_ID_67183 Human_SNP_ID_1751156 m1A Human chr1 + 6207523 6207515 6207523 GACCTGGAGTGCAGCGAGCAGGCAGGGGCGGCAGGGCGGGTGGGTGAGGAGCAGAGGGTACCCGG GACCTGGAGTGCAGCGAGCAGGCAG________GGGCGGGTGGGTGAGGAGCAGAGGGTACCCGG GGGGCGGCA G RNF207 Ensembl:ENSG00000158286 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6207472..6207610 26863196 MeRIP-seq:(Medium) rs750256229 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_25351,Human_RBP_ID_745243 67184 RMVar_ID_67184 Human_SNP_ID_1756362 m1A Human chr1 - 6224144 6224144 6224144 TTACCATAGCTTATATTCTCAATTTCAATGCCAGTCTCAGAACTCTTGTTTTCTGTGTTCTGTTC TTACCATAGCTTATATTCTCAATTTCAATGCCGGTCTCAGAACTCTTGTTTTCTGTGTTCTGTTC T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:6224051..6224425 32194978 MeRIP-seq:(Medium) rs907941387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1433435,Human_RBP_ID_1751991,Human_RBP_ID_3319046,Human_RBP_ID_5849376,Human_RBP_ID_8751000,Human_RBP_ID_11062689,Human_RBP_ID_17219491,Human_RBP_ID_17336677,Human_RBP_ID_17454183,Human_RBP_ID_18232610,Human_RBP_ID_23406252,Human_RBP_ID_27596952 Human_miRNA_ID_469798,Human_miRNA_ID_475628,Human_miRNA_ID_3084996 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 67185 RMVar_ID_67185 Human_SNP_ID_1756553 m1A Human chr1 + 6224887 6224887 6224887 CGTCTTTCACCCATGTTCCGCCTTGATTCGGCATAAGGACAGACTGCTCCAGTGGGGCCTTGGGT CGTCTTTCACCCATGTTCCGCCTTGATTCGGCCTAAGGACAGACTGCTCCAGTGGGGCCTTGGGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:6224651..6225125 32194978 MeRIP-seq:(Medium) rs887911942 Functional Loss SNV dbSNP153 33..33 33 - - - 67186 RMVar_ID_67186 Human_SNP_ID_1756554 m1A Human chr1 + 6224887 6224887 6224887 CGTCTTTCACCCATGTTCCGCCTTGATTCGGCATAAGGACAGACTGCTCCAGTGGGGCCTTGGGT CGTCTTTCACCCATGTTCCGCCTTGATTCGGCGTAAGGACAGACTGCTCCAGTGGGGCCTTGGGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:6224651..6225125 32194978 MeRIP-seq:(Medium) rs887911942 Functional Loss SNV dbSNP153 33..33 33 - - - 67187 RMVar_ID_67187 Human_SNP_ID_1759756 m1A Human chr1 + 6235878 6235878 6235878 CAGGAAGGTGGCGAGGCTGAGACGCGCCTCAGAGCCCGGCGGAGCCCGCGCCGCGCAGCCCGCCA CAGGAAGGTGGCGAGGCTGAGACGCGCCTCAGCGCCCGGCGGAGCCCGCGCCGCGCAGCCCGCCA A C LINC00337 Ensembl:ENSG00000225077 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:6235726..6236000 26863410 MeRIP-seq:(Medium) rs1215133562 Functional Loss SNV dbSNP153 33..33 33 - - - 67188 RMVar_ID_67188 Human_SNP_ID_1763244 m1A Human chr1 + 6247686 6247686 6247686 ACAAATGAGTGAAAACCTAAGGTGACAAGTGGACAGACGCCCCCCAGATGGAGGAGACACTGGCT ACAAATGAGTGAAAACCTAAGGTGACAAGTGGTCAGACGCCCCCCAGATGGAGGAGACACTGGCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6247644..6247744 32194978 MeRIP-seq:(Medium) rs1295958877 Functional Loss SNV dbSNP153 33..33 33 - - - 67189 RMVar_ID_67189 Human_SNP_ID_1763936 m1A Human chr1 - 6249579 6249579 6249579 CGGGCCCTTCCCCGCTGCGCCCGCCGCCCCCGACGGCGCAGATCCCGGAGAGGCCCCGACGCCCC CGGGCCCTTCCCCGCTGCGCCCGCCGCCCCCGGCGGCGCAGATCCCGGAGAGGCCCCGACGCCCC T C GPR153 Ensembl:ENSG00000158292 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6249533..6249683 26863196 MeRIP-seq:(Medium) rs1419081820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98596,RMVar_hsa_circ_108743,RMVar_hsa_circ_125417,RMVar_hsa_circ_108023,RMVar_hsa_circ_128620,RMVar_hsa_circ_128621,RMVar_hsa_circ_128622,RMVar_hsa_circ_128619 67190 RMVar_ID_67190 Human_SNP_ID_1763960 m1A Human chr1 + 6249624 6249624 6249624 GCGCAGCGGGGAAGGGCCCGGGCGGGCGGCGCAGGGCCTGTGGCTCGCACTCGAAGGCGGTCAGG GCGCAGCGGGGAAGGGCCCGGGCGGGCGGCGCTGGGCCTGTGGCTCGCACTCGAAGGCGGTCAGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:6249418..6249785 26863410 MeRIP-seq:(Medium) rs960991465 Functional Loss SNV dbSNP153 33..33 33 - - - 67191 RMVar_ID_67191 Human_SNP_ID_1765504 m1A Human chr1 - 6254617 6254617 6254617 TCGTGTCCACCTTCTACACCCTCACCCTGGCCACCTGTTTCTCTGTCACCTCCCTCTCCTACCAC TCGTGTCCACCTTCTACACCCTCACCCTGGCCGCCTGTTTCTCTGTCACCTCCCTCTCCTACCAC T C GPR153 Ensembl:ENSG00000158292 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6254567..6254767 26863196 MeRIP-seq:(Medium) rs1469956097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_11807 Human_miRNA_ID_2876204,Human_miRNA_ID_2889091 RMVar_hsa_circ_108023,RMVar_hsa_circ_128622 67192 RMVar_ID_67192 Human_SNP_ID_1765523 m1A Human chr1 + 6254646 6254646 6254646 AGGTGGCCAGGGTGAGGGTGTAGAAGGTGGACACGAAGACCTTGCAGAGACCCTCATTCCACTCG AGGTGGCCAGGGTGAGGGTGTAGAAGGTGGACGCGAAGACCTTGCAGAGACCCTCATTCCACTCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6254596..6254699 26863196 MeRIP-seq:(Medium) rs1370552631 Functional Loss SNV dbSNP153 33..33 33 - - - 67193 RMVar_ID_67193 Human_SNP_ID_1765531 m1A Human chr1 - 6254667 6254667 6254667 GCGGCGGCAGCGCCCCGACTTCGAGTGGAATGAGGGTCTCTGCAAGGTCTTCGTGTCCACCTTCT GCGGCGGCAGCGCCCCGACTTCGAGTGGAATGTGGGTCTCTGCAAGGTCTTCGTGTCCACCTTCT T A GPR153 Ensembl:ENSG00000158292 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6254617..6260875 32194978 MeRIP-seq:(Medium) rs755220018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108023,RMVar_hsa_circ_128622 67194 RMVar_ID_67194 Human_SNP_ID_1768500 m1A Human chr1 + 6264587 6264587 6264587 TTGCCATGGCTACTCGAGGCACCAGTGGCAGGAGGAGGGAGTCTAGGGCTGAGGCTCCGCGTGGC TTGCCATGGCTACTCGAGGCACCAGTGGCAGGGGGAGGGAGTCTAGGGCTGAGGCTCCGCGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6264538..6264638 26863196 MeRIP-seq:(Medium) rs200121112 Functional Loss SNV dbSNP153 33..33 33 - - - 67195 RMVar_ID_67195 Human_SNP_ID_1772188 m1A Human chr1 - 6277566 6277566 6277566 TGTCTGTAACGGGGGAGCTTGGGGACAGTGACACACCCGAGGCCACCCGGCTAGGACGGGGCAGG TGTCTGTAACGGGGGAGCTTGGGGACAGTGACGCACCCGAGGCCACCCGGCTAGGACGGGGCAGG T C ACOT7 Ensembl:ENSG00000097021 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6277563..6277662 26863196 MeRIP-seq:(Medium) rs944652844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83681,RMVar_hsa_circ_112260,RMVar_hsa_circ_112671,RMVar_hsa_circ_93326,RMVar_hsa_circ_106361,RMVar_hsa_circ_89620,RMVar_hsa_circ_128625,RMVar_hsa_circ_128627,RMVar_hsa_circ_128629,RMVar_hsa_circ_128631,RMVar_hsa_circ_80949,RMVar_hsa_circ_128630,RMVar_hsa_circ_128628,RMVar_hsa_circ_128626 67196 RMVar_ID_67196 Human_SNP_ID_1773141 m1A Human chr1 - 6281128 6281128 6281128 TCTTCACCTACGTGTCGCTGAGCCAGGAAGGCAGGTCGCTGCCTGTGCCCCAGCTGGTGGTGAGT TCTTCACCTACGTGTCGCTGAGCCAGGAAGGCTGGTCGCTGCCTGTGCCCCAGCTGGTGGTGAGT T A ACOT7 Ensembl:ENSG00000097021 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6264516..6281225 32194978 MeRIP-seq:(Medium) rs372605671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4062332,Human_RBP_ID_18579091,Human_RBP_ID_22428967 Human_Splice_Rec_11829,Human_Splice_Rec_11845,Human_Splice_Rec_11861,Human_Splice_Rec_11877,Human_Splice_Rec_11895,Human_Splice_Rec_11913,Human_Splice_Rec_11929,Human_Splice_Rec_11945 RMVar_hsa_circ_83681,RMVar_hsa_circ_112260,RMVar_hsa_circ_112671,RMVar_hsa_circ_93326,RMVar_hsa_circ_106361,RMVar_hsa_circ_89620,RMVar_hsa_circ_47935,RMVar_hsa_circ_128625,RMVar_hsa_circ_128627,RMVar_hsa_circ_128629,RMVar_hsa_circ_128631,RMVar_hsa_circ_80949,RMVar_hsa_circ_128630,RMVar_hsa_circ_128628,RMVar_hsa_circ_128626,RMVar_hsa_circ_74572,RMVar_hsa_circ_296017,RMVar_hsa_circ_51563,RMVar_hsa_circ_128632,RMVar_hsa_circ_7465 67197 RMVar_ID_67197 Human_SNP_ID_1791844 m1A Human chr1 + 6349861 6349861 6349861 CATTGCCGGCCACGTTGGCATCATCTGGCCGCATGATCCTAGGGCAGAGGAGAAGCAGGATGAGG CATTGCCGGCCACGTTGGCATCATCTGGCCGCGTGATCCTAGGGCAGAGGAGAAGCAGGATGAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6349826..6349910 26863196 MeRIP-seq:(Medium) rs762286520 Functional Loss SNV dbSNP153 33..33 33 - - - 67198 RMVar_ID_67198 Human_SNP_ID_1793520 m1A Human chr1 - 6356393 6356384 6356393 GCTGAGGGTGCTGGGCAGGGCTGAGGGTGCTGAGGGTGCTGCCGCTGCTGCCTCGGGGCTCCCCT GCTGAGGGTGCTGGGCAGGGCTGAGGGTGCTG_________CCGCTGCTGCCTCGGGGCTCCCCT GCAGCACCCT G ACOT7 Ensembl:ENSG00000097021 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6356391..6356637 26863196 MeRIP-seq:(Medium) rs796908651 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_112671,RMVar_hsa_circ_106361,RMVar_hsa_circ_128631,RMVar_hsa_circ_128630 67199 RMVar_ID_67199 Human_SNP_ID_1803480 m1A Human chr1 + 6393324 6393324 6393324 TGGGCCCGACATGCTGGGGGCTGCGGCGGCGGATGCGGCGGGCGGCTGCAGAAGGGCGCAGGTGT TGGGCCCGACATGCTGGGGGCTGCGGCGGCGGCTGCGGCGGGCGGCTGCAGAAGGGCGCAGGTGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:6385804..6393447;chr1:6393215..6393474;chr1:6393211..6393478;chr1:6393215..6393428 26863196 MeRIP-seq:(Medium) rs1458312942 Functional Loss SNV dbSNP153 33..33 33 - - - 67200 RMVar_ID_67200 Human_SNP_ID_1803626 m1A Human chr1 - 6393577 6393577 6393577 ACCTTCTGGAAGCGGCGGCTGCCTGGGCCCCCACGCCGCCAGAATCGTACGCCCGCGCGAGCTCT ACCTTCTGGAAGCGGCGGCTGCCTGGGCCCCCCCGCCGCCAGAATCGTACGCCCGCGCGAGCTCT T G ACOT7 Ensembl:ENSG00000097021 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:6393530..6393726;chr1:6393533..6393727 26863196 MeRIP-seq:(Medium) rs1398093869 Functional Loss SNV dbSNP153 33..33 33 - - - 67201 RMVar_ID_67201 Human_SNP_ID_1812410 m1A Human chr1 + 6424820 6424820 6424820 AGCGGAGCGCCAGGCAGCGCGGAGCGGAGGCCAGGCCCACAGCCGCTCCGCCTCCCGGCCCGCAG AGCGGAGCGCCAGGCAGCGCGGAGCGGAGGCCCGGCCCACAGCCGCTCCGCCTCCCGGCCCGCAG A C ESPN Ensembl:ENSG00000187017 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6424811..6424902 26863196 MeRIP-seq:(Medium) rs188079860 Functional Loss SNV dbSNP153 33..33 33 - - - 67202 RMVar_ID_67202 Human_SNP_ID_1812411 m1A Human chr1 + 6424820 6424820 6424820 AGCGGAGCGCCAGGCAGCGCGGAGCGGAGGCCAGGCCCACAGCCGCTCCGCCTCCCGGCCCGCAG AGCGGAGCGCCAGGCAGCGCGGAGCGGAGGCCGGGCCCACAGCCGCTCCGCCTCCCGGCCCGCAG A G ESPN Ensembl:ENSG00000187017 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6424811..6424902 26863196 MeRIP-seq:(Medium) rs188079860 Functional Loss SNV dbSNP153 33..33 33 - - - 67203 RMVar_ID_67203 Human_SNP_ID_1812427 m1A Human chr1 - 6424880 6424880 6424880 CAGGACGCCATGCACGTGTTCTTGCGGGCCAGAGGAGCCCGCGGTGCGGCCGTCGGGGATCTGCG CAGGACGCCATGCACGTGTTCTTGCGGGCCAGGGGAGCCCGCGGTGCGGCCGTCGGGGATCTGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6424846..6424978 26863196 MeRIP-seq:(Medium) rs1426175924 Functional Loss SNV dbSNP153 33..33 33 - - - 67204 RMVar_ID_67204 Human_SNP_ID_1812546 m1A Human chr1 + 6425160 6425160 6425160 AAGCCGCCCTCCCCGCCGCGGCCCGCGCCCGCAACGGCGCCACACCGGCCCACGACGCCTCCGCC AAGCCGCCCTCCCCGCCGCGGCCCGCGCCCGCCACGGCGCCACACCGGCCCACGACGCCTCCGCC A C ESPN Ensembl:ENSG00000187017 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6425131..6425196 26863196 MeRIP-seq:(Medium) rs746822694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22532028 Human_Splice_Rec_11991,Human_Splice_Rec_12015 67205 RMVar_ID_67205 Human_SNP_ID_1818235 m1A Human chr1 - 6445947 6445947 6445947 CAGTCCCCCTGCTGGGAGGCAGGCAGGGGGTGAGGGCTCACTACCTCCTTCTTGAGGGCCTCTGT CAGTCCCCCTGCTGGGAGGCAGGCAGGGGGTGGGGGCTCACTACCTCCTTCTTGAGGGCCTCTGT T C AL031848.1 Ensembl:ENSG00000231868 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6445941..6446006 26863196 MeRIP-seq:(Medium) rs768697143 Functional Loss SNV dbSNP153 33..33 33 - - - 67206 RMVar_ID_67206 Human_SNP_ID_1822571 m1A Human chr1 - 6459974 6459974 6459974 CCTCTTTCCTGAGGCAGTGGGGAGGGGGGCAGACCCGGTGAAGTCTGGGGCCAGATACCCAGGCT CCTCTTTCCTGAGGCAGTGGGGAGGGGGGCAGGCCCGGTGAAGTCTGGGGCCAGATACCCAGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6459969..6460212 26863196 MeRIP-seq:(Medium) rs1463799077 Functional Loss SNV dbSNP153 33..33 33 - - - 67207 RMVar_ID_67207 Human_SNP_ID_1825457 m1A Human chr1 - 6468195 6468195 6468195 CGCCCCACCTGCTCAAGTCTAAGTCCGAGGCCAGCCTCCTCCAGCTGCTGGCAGGGGCTGGCACC CGCCCCACCTGCTCAAGTCTAAGTCCGAGGCCGGCCTCCTCCAGCTGCTGGCAGGGGCTGGCACC T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6468144..6468504 26863196 MeRIP-seq:(Medium) rs374340207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_12721 67208 RMVar_ID_67208 Human_SNP_ID_1825464 m1A Human chr1 + 6468208 6468202 6468208 GCCAGCAGCTGGAGGAGGCTGGCCTCGGACTTAGACTTGAGCAGGTGGGGCGGGCAGCTCAACAG GCCAGCAGCTGGAGGAGGCTGGCCTCG______GACTTGAGCAGGTGGGGCGGGCAGCTCAACAG GGACTTA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6468158..6468345 26863196 MeRIP-seq:(Medium) rs1557735067 Functional Loss DEL dbSNP153 28..33 33 - - - 67209 RMVar_ID_67209 Human_SNP_ID_1825757 m1A Human chr1 + 6469091 6469091 6469091 GCTGCCGCTGCTTTTCCGCATGATGGTAGGGGAGCTGGCAGCTGAAGTGCCACTGTCCTCGCCTT GCTGCCGCTGCTTTTCCGCATGATGGTAGGGGGGCTGGCAGCTGAAGTGCCACTGTCCTCGCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6469046..6469174 26863196 MeRIP-seq:(Medium) rs373793845 Functional Loss SNV dbSNP153 33..33 33 - - - 67210 RMVar_ID_67210 Human_SNP_ID_1826320 m1A Human chr1 - 6470523 6470523 6470523 GCATCGACGCCTACGAGGTGGTGGAAAGCAGCAGCGACGAAGTGGACAAGGTGGGCGTGTGTGTC GCATCGACGCCTACGAGGTGGTGGAAAGCAGCTGCGACGAAGTGGACAAGGTGGGCGTGTGTGTC T A PLEKHG5 Ensembl:ENSG00000171680 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6470324..6471267 32194978 MeRIP-seq:(Medium) rs747711931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_12409,Human_Splice_Rec_12449,Human_Splice_Rec_12489,Human_Splice_Rec_12529,Human_Splice_Rec_12571,Human_Splice_Rec_12613,Human_Splice_Rec_12655,Human_Splice_Rec_12671,Human_Splice_Rec_12711,Human_Splice_Rec_12753,Human_Splice_Rec_12793,Human_Splice_Rec_12835,Human_Splice_Rec_12877 RMVar_hsa_circ_47974,RMVar_hsa_circ_85259,RMVar_hsa_circ_127949,RMVar_hsa_circ_128640,RMVar_hsa_circ_128641 67211 RMVar_ID_67211 Human_SNP_ID_1826321 m1A Human chr1 - 6470523 6470523 6470523 GCATCGACGCCTACGAGGTGGTGGAAAGCAGCAGCGACGAAGTGGACAAGGTGGGCGTGTGTGTC GCATCGACGCCTACGAGGTGGTGGAAAGCAGCCGCGACGAAGTGGACAAGGTGGGCGTGTGTGTC T G PLEKHG5 Ensembl:ENSG00000171680 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6470324..6471267 32194978 MeRIP-seq:(Medium) rs747711931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_12409,Human_Splice_Rec_12449,Human_Splice_Rec_12489,Human_Splice_Rec_12529,Human_Splice_Rec_12571,Human_Splice_Rec_12613,Human_Splice_Rec_12655,Human_Splice_Rec_12671,Human_Splice_Rec_12711,Human_Splice_Rec_12753,Human_Splice_Rec_12793,Human_Splice_Rec_12835,Human_Splice_Rec_12877 RMVar_hsa_circ_47974,RMVar_hsa_circ_85259,RMVar_hsa_circ_127949,RMVar_hsa_circ_128640,RMVar_hsa_circ_128641 67212 RMVar_ID_67212 Human_SNP_ID_1826834 m1A Human chr1 - 6471467 6471467 6471467 GGCTTCAAGATGGTACGGGCGGGGCCGGGCGCAGGCGGGGGCACTGAGGCAGGGCTGGGGCGCCG GGCTTCAAGATGGTACGGGCGGGGCCGGGCGCGGGCGGGGGCACTGAGGCAGGGCTGGGGCGCCG T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6471461..6471551 26863196 MeRIP-seq:(Medium) rs752026773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22970,Human_RBP_ID_19036505 RMVar_hsa_circ_47974,RMVar_hsa_circ_85259,RMVar_hsa_circ_128641 67213 RMVar_ID_67213 Human_SNP_ID_1827545 m1A Human chr1 - 6473327 6473327 6473327 CAGCGGCAGCAGTGGCAGCACCAACACTGGCGACAGCTGGAAGAACCGGGCGGCCAGTCGCTTCA CAGCGGCAGCAGTGGCAGCACCAACACTGGCGGCAGCTGGAAGAACCGGGCGGCCAGTCGCTTCA T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6473203..6473407 26863196 MeRIP-seq:(Medium) rs199794578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_12395,Human_Splice_Rec_12435,Human_Splice_Rec_12475,Human_Splice_Rec_12515,Human_Splice_Rec_12557,Human_Splice_Rec_12599,Human_Splice_Rec_12641,Human_Splice_Rec_12697,Human_Splice_Rec_12739,Human_Splice_Rec_12779,Human_Splice_Rec_12821,Human_Splice_Rec_12863 Clinvar_Rec_269 RMVar_hsa_circ_47974 67214 RMVar_ID_67214 Human_SNP_ID_1828583 m1A Human chr1 + 6475971 6475971 6475971 ATCCACAGAGCTCTCCTCCTCCTCCTCCTCCAAGTCCACTGCGGGGCTGGTGCGCGGCGGGCATG ATCCACAGAGCTCTCCTCCTCCTCCTCCTCCAGGTCCACTGCGGGGCTGGTGCGCGGCGGGCATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6475076..6485461 32194978 MeRIP-seq:(Medium) rs1405993368 Functional Loss SNV dbSNP153 33..33 33 - - - 67215 RMVar_ID_67215 Human_SNP_ID_1831195 m1A Human chr1 - 6485703 6485703 6485703 TGTGGAGTCCCCGGGTCTGGGCAGAGGCGGGGAGGCGGGGGGTCGCCCGGGCAGGCGGAGGCGGG TGTGGAGTCCCCGGGTCTGGGCAGAGGCGGGGGGGCGGGGGGTCGCCCGGGCAGGCGGAGGCGGG T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6485699..6485917 26863196 MeRIP-seq:(Medium) rs1048793265 Functional Loss SNV dbSNP153 33..33 33 - - - 67216 RMVar_ID_67216 Human_SNP_ID_1832285 m1A Human chr1 + 6490152 6490152 6490152 CTCCCAGCCACGCCGCGCGCCCGGGCCCCTCCAGGATCCCCCTGCCCCGCCAATACCCCCCATAC CTCCCAGCCACGCCGCGCGCCCGGGCCCCTCCGGGATCCCCCTGCCCCGCCAATACCCCCCATAC A G lnc-ESPN-4 RNACentral:URS0000D587A6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6490150..6490231 26863196 MeRIP-seq:(Medium) rs898809492 Functional Loss SNV dbSNP153 33..33 33 - - - 67217 RMVar_ID_67217 Human_SNP_ID_1834040 m1A Human chr1 - 6497294 6497294 6497294 TCCATGGGTGAGTGCAGGCGGGGACCCGGCGGACGCGGGGCGGGGTCCTGGGGGGCCGGGCCGGC TCCATGGGTGAGTGCAGGCGGGGACCCGGCGGGCGCGGGGCGGGGTCCTGGGGGGCCGGGCCGGC T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6497287..6497389 26863196 MeRIP-seq:(Medium) rs766069073 Functional Loss SNV dbSNP153 33..33 33 - - - 67218 RMVar_ID_67218 Human_SNP_ID_1834934 m1A Human chr1 - 6500668 6500667 6500668 AAGGGGGGTAGTTCATGGTTCCAGGTCTGGCTAGGGGTGGGGGGAGTTCAGGGTTCCAGGTTTGC AAGGGGGGTAGTTCATGGTTCCAGGTCTGGCT_GGGGTGGGGGGAGTTCAGGGTTCCAGGTTTGC CT C PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6500666..6500789 26863196 MeRIP-seq:(Medium) rs1557767866 Functional Loss DEL dbSNP153 33..33 33 - - - 67219 RMVar_ID_67219 Human_SNP_ID_1835117 m1A Human chr1 + 6501257 6501257 6501257 CAGGCCCCTCACTCCGCTACTTGCCGGACACAACTGAGCTTCTGACCCCAGCCCAGCCCTTCTTG CAGGCCCCTCACTCCGCTACTTGCCGGACACAGCTGAGCTTCTGACCCCAGCCCAGCCCTTCTTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6501254..6501345 26863196 MeRIP-seq:(Medium) rs1557768134 Functional Loss SNV dbSNP153 33..33 33 - - - 67220 RMVar_ID_67220 Human_SNP_ID_1835936 m1A Human chr1 - 6504403 6504403 6504403 AGGTACAGTGTCCCACAGGCCCCAGCAACTCCAGGCCCCATCGGGACGTGCGCAGAAGGCAGGGA AGGTACAGTGTCCCACAGGCCCCAGCAACTCCCGGCCCCATCGGGACGTGCGCAGAAGGCAGGGA T G PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6504380..6504464 26863196 MeRIP-seq:(Medium) rs1485099172 Functional Loss SNV dbSNP153 33..33 33 - - - 67221 RMVar_ID_67221 Human_SNP_ID_1840251 m1A Human chr1 + 6519931 6519931 6519931 CGTCCCTCCTTTCCAGGAAAGCAACACCACAGAGACCCCGGCCTCTGCAATCCCAGCAGCCAGCA CGTCCCTCCTTTCCAGGAAAGCAACACCACAGGGACCCCGGCCTCTGCAATCCCAGCAGCCAGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6519880..6519968 26863196 MeRIP-seq:(Medium) rs1434371838 Functional Loss SNV dbSNP153 33..33 33 - - - 67222 RMVar_ID_67222 Human_SNP_ID_1843612 m1A Human chr1 - 6531880 6531880 6531880 TTCTGTGTGCTGGGCGCTCTCCTAACCACTACATAACTCCTCGCTCATTTAATCCTCAGAACATC TTCTGTGTGCTGGGCGCTCTCCTAACCACTACTTAACTCCTCGCTCATTTAATCCTCAGAACATC T A NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:6531877..6532060 26863196 MeRIP-seq:(Medium) rs1225093115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8973088 RMVar_hsa_circ_82584,RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_91307,RMVar_hsa_circ_377994,RMVar_hsa_circ_128652,RMVar_hsa_circ_128649,RMVar_hsa_circ_65372,RMVar_hsa_circ_79485,RMVar_hsa_circ_128650,RMVar_hsa_circ_272524,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_370006,RMVar_hsa_circ_300326,RMVar_hsa_circ_128654,RMVar_hsa_circ_128655,RMVar_hsa_circ_128653 67223 RMVar_ID_67223 Human_SNP_ID_1847789 m1A Human chr1 - 6546684 6546682 6546684 GAGGAAGGGGGAGGTAACCATGCAGCAGAGAGAGGAGAGGCTGCTGGAACTATGTAAGTTGGCTA GAGGAAGGGGGAGGTAACCATGCAGCAGAGAG__GAGAGGCTGCTGGAACTATGTAAGTTGGCTA CCT C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6546647..6546887 26863196 MeRIP-seq:(Medium) rs1427476371 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_222670,Human_RBP_ID_803883,Human_RBP_ID_5854287 RMVar_hsa_circ_82584,RMVar_hsa_circ_119236,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_128655,RMVar_hsa_circ_378388,RMVar_hsa_circ_289399,RMVar_hsa_circ_128662,RMVar_hsa_circ_128660,RMVar_hsa_circ_342850,RMVar_hsa_circ_297903,RMVar_hsa_circ_128663,RMVar_hsa_circ_318598 67224 RMVar_ID_67224 Human_SNP_ID_1850109 m1A Human chr1 + 6554297 6554297 6554297 TGTTGGGTCTCCGGGCCGCCGCCGCGCGCGACACCTGGCGGGCTCCCTCCCTCCAGTCCACGCCG TGTTGGGTCTCCGGGCCGCCGCCGCGCGCGACCCCTGGCGGGCTCCCTCCCTCCAGTCCACGCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6554248..6554391 26863196 MeRIP-seq:(Medium) rs1211848195 Functional Loss SNV dbSNP153 33..33 33 - - - 67225 RMVar_ID_67225 Human_SNP_ID_1850259 m1A Human chr1 + 6554466 6554466 6554466 GGCCTTGCGGACCCGCAGCCAAGTGGAACGGCAGGAACCCCGCTTTAGCAGCAGTCCCGAGTCCG GGCCTTGCGGACCCGCAGCCAAGTGGAACGGCGGGAACCCCGCTTTAGCAGCAGTCCCGAGTCCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:6554336..6554465 26863196 MeRIP-seq:(Medium) rs12742808 Functional Loss SNV dbSNP153 33..33 33 - - - 67226 RMVar_ID_67226 Human_SNP_ID_1859260 m1A Human chr1 - 6585189 6585189 6585189 GCCCAGATGCTCCCCAGTCACCCACTTGGTCAACTTCCTCACCTCCTTTGAGTCTTTGCTTAAAT GCCCAGATGCTCCCCAGTCACCCACTTGGTCAGCTTCCTCACCTCCTTTGAGTCTTTGCTTAAAT T C HSALNG0000533 RNACentral:URS0000EAFE07 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6585163..6585234 26863196 MeRIP-seq:(Medium) rs1278015256 Functional Loss SNV dbSNP153 33..33 33 - - - 67227 RMVar_ID_67227 Human_SNP_ID_1863876 m1A Human chr1 - 6599177 6599177 6599177 GCCGGCTCTATGCCATCGGCTCCCTGGCTGGCAAGGAGACCATGGTGATGCAGTGCTACGACCCG GCCGGCTCTATGCCATCGGCTCCCTGGCTGGCCAGGAGACCATGGTGATGCAGTGCTACGACCCG T G KLHL21 Ensembl:ENSG00000162413 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6599126..6599376 32194978 MeRIP-seq:(Medium) rs1432268345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8753434,Human_RBP_ID_9269570,Human_RBP_ID_9357975,Human_RBP_ID_22022662,Human_RBP_ID_23112636 Human_miRNA_ID_2233705,Human_miRNA_ID_2396581 RMVar_hsa_circ_128670,RMVar_hsa_circ_128669,RMVar_hsa_circ_328707,RMVar_hsa_circ_291317 67228 RMVar_ID_67228 Human_SNP_ID_1868718 m1A Human chr1 - 6613826 6613826 6613826 CGATGCAGCTCCCGCGGCGGTAGAGGCGGGAGAGTGGCTGCAGGGGGCGGCGGCGGCGGCGGTGA CGATGCAGCTCCCGCGGCGGTAGAGGCGGGAGGGTGGCTGCAGGGGGCGGCGGCGGCGGCGGTGA T C KLHL21 Ensembl:ENSG00000162413 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:6613780..6616784;chr1:6613783..6614050 26863196 MeRIP-seq:(Medium) rs1313875555 Functional Loss SNV dbSNP153 33..33 33 - - - 67229 RMVar_ID_67229 Human_SNP_ID_1868719 m1A Human chr1 - 6613828 6613828 6613828 GACGATGCAGCTCCCGCGGCGGTAGAGGCGGGAGAGTGGCTGCAGGGGGCGGCGGCGGCGGCGGT GACGATGCAGCTCCCGCGGCGGTAGAGGCGGGGGAGTGGCTGCAGGGGGCGGCGGCGGCGGCGGT T C KLHL21 Ensembl:ENSG00000162413 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6613781..6614136 26863196 MeRIP-seq:(Medium) rs931092668 Functional Loss SNV dbSNP153 33..33 33 - - - 67230 RMVar_ID_67230 Human_SNP_ID_1868725 m1A Human chr1 - 6613837 6613837 6613837 ACCGGAGTGGACGATGCAGCTCCCGCGGCGGTAGAGGCGGGAGAGTGGCTGCAGGGGGCGGCGGC ACCGGAGTGGACGATGCAGCTCCCGCGGCGGTGGAGGCGGGAGAGTGGCTGCAGGGGGCGGCGGC T C KLHL21 Ensembl:ENSG00000162413 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:6613792..6614008 26863196 MeRIP-seq:(Medium) rs975206375 Functional Loss SNV dbSNP153 33..33 33 - - - 67231 RMVar_ID_67231 Human_SNP_ID_1871914 m1A Human chr1 - 6622285 6622285 6622285 TCAACCCCCCAACCAACTCCCTTTCCACAGAGAAGTGGCCACATTGTCCCTTTTAACAAACAGAA TCAACCCCCCAACCAACTCCCTTTCCACAGAGTAGTGGCCACATTGTCCCTTTTAACAAACAGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:6622242..6622377 26863196 MeRIP-seq:(Medium) rs553701425 Functional Loss SNV dbSNP153 33..33 33 - - - 67232 RMVar_ID_67232 Human_SNP_ID_1872862 m1A Human chr1 + 6625264 6625264 6625264 GCGCGGCCCGGCAGTGCTGCAACCGCTACAGCAGCCGCAGGAAGCAGCTCACCTTCCACCGGTAA GCGCGGCCCGGCAGTGCTGCAACCGCTACAGCGGCCGCAGGAAGCAGCTCACCTTCCACCGGTAA A G THAP3 Ensembl:ENSG00000041988 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6625214..6625640 26863196 MeRIP-seq:(Medium) rs1156539812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073484,Human_RBP_ID_5312293 Human_Splice_Rec_13059,Human_Splice_Rec_13067,Human_Splice_Rec_13069,Human_Splice_Rec_13077,Human_Splice_Rec_13085,Human_Splice_Rec_13091,Human_Splice_Rec_13101 67233 RMVar_ID_67233 Human_SNP_ID_1872867 m1A Human chr1 + 6625270 6625270 6625270 CCCGGCAGTGCTGCAACCGCTACAGCAGCCGCAGGAAGCAGCTCACCTTCCACCGGTAAGAGGCG CCCGGCAGTGCTGCAACCGCTACAGCAGCCGCGGGAAGCAGCTCACCTTCCACCGGTAAGAGGCG A G THAP3 Ensembl:ENSG00000041988 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6625220..6625599 26863196 MeRIP-seq:(Medium) rs950385390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073484,Human_RBP_ID_5312293 Human_Splice_Rec_13059,Human_Splice_Rec_13067,Human_Splice_Rec_13069,Human_Splice_Rec_13077,Human_Splice_Rec_13085,Human_Splice_Rec_13091,Human_Splice_Rec_13101 67234 RMVar_ID_67234 Human_SNP_ID_1875252 m1A Human chr1 + 6633037 6633037 6633037 GTCCAGCCGCCTCCGTGCTTGCAAAGGGCACCAGGGACTCCAGGCCAGACTTGGGCCAGAGCAGC GTCCAGCCGCCTCCGTGCTTGCAAAGGGCACCGGGGACTCCAGGCCAGACTTGGGCCAGAGCAGC A G THAP3 Ensembl:ENSG00000041988 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3174820 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_7969,GWAS_ID_7970,GWAS_ID_7971,GWAS_ID_7972,GWAS_ID_7973,GWAS_ID_7974,GWAS_ID_7975,GWAS_ID_7976,GWAS_ID_7977,GWAS_ID_7978,GWAS_ID_7979,GWAS_ID_7980,GWAS_ID_7981,GWAS_ID_7982,GWAS_ID_7983,GWAS_ID_7984,GWAS_ID_7985,GWAS_ID_7986,GWAS_ID_7987,GWAS_ID_7988,GWAS_ID_7989,GWAS_ID_7990,GWAS_ID_7991,GWAS_ID_7992,GWAS_ID_7993,GWAS_ID_7994,GWAS_ID_7995,GWAS_ID_7996,GWAS_ID_7997,GWAS_ID_7998,GWAS_ID_7999,GWAS_ID_8000,GWAS_ID_8001,GWAS_ID_8002,GWAS_ID_8003,GWAS_ID_8004,GWAS_ID_8005,GWAS_ID_8006,GWAS_ID_8007,GWAS_ID_8008,GWAS_ID_8009,GWAS_ID_8010,GWAS_ID_8011,GWAS_ID_8012,GWAS_ID_8013,GWAS_ID_8014,GWAS_ID_8015,GWAS_ID_8016,GWAS_ID_8017,GWAS_ID_8018,GWAS_ID_8019,GWAS_ID_8020 67235 RMVar_ID_67235 Human_SNP_ID_1876118 m1A Human chr1 - 6635263 6635263 6635263 AGCGTGAGCCACTTCTGCAGTCCACGCTGAACATGGGAAACAACCTGAAAAGCAGGCAGGCCTCC AGCGTGAGCCACTTCTGCAGTCCACGCTGAACGTGGGAAACAACCTGAAAAGCAGGCAGGCCTCC T C DNAJC11 Ensembl:ENSG00000007923 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6635213..6635487 32194978 MeRIP-seq:(Medium) rs1165787358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4063877 67236 RMVar_ID_67236 Human_SNP_ID_1876760 m1A Human chr1 - 6637296 6637296 6637296 TCAATGCCTGGTACGGGAAGTTTGTCAATGACAAGAGCAGGAAGAGCGAGAAGGTGAAGGTGATT TCAATGCCTGGTACGGGAAGTTTGTCAATGACGAGAGCAGGAAGAGCGAGAAGGTGAAGGTGATT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6636227..6637534 32194978 MeRIP-seq:(Medium) rs1194553963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1752686,Human_RBP_ID_3932572,Human_RBP_ID_4063896,Human_RBP_ID_18967058,Human_RBP_ID_26310123 Human_Splice_Rec_13116,Human_Splice_Rec_13117,Human_Splice_Rec_13160,Human_Splice_Rec_13161,Human_Splice_Rec_13188,Human_Splice_Rec_13189,Human_Splice_Rec_13202 Human_miRNA_ID_2937850 RMVar_hsa_circ_3677,RMVar_hsa_circ_109345,RMVar_hsa_circ_128673 67237 RMVar_ID_67237 Human_SNP_ID_1881411 m1A Human chr1 - 6654037 6654037 6654037 TTCTGCTGACGGCTTGTTTTTCTGCCCCAGGGAACGATCAGCGTTGGAGTAGATGCCACCGACCT TTCTGCTGACGGCTTGTTTTTCTGCCCCAGGGTACGATCAGCGTTGGAGTAGATGCCACCGACCT T A DNAJC11 Ensembl:ENSG00000007923 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6654001..6654050 26863196 MeRIP-seq:(Medium) rs780020310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853629,Human_RBP_ID_2161454,Human_RBP_ID_26310131 Human_Splice_Rec_13126,Human_Splice_Rec_13142,Human_Splice_Rec_13172,Human_Splice_Rec_13210,Human_Splice_Rec_13222,Human_Splice_Rec_13232,Human_Splice_Rec_13242 RMVar_hsa_circ_26219,RMVar_hsa_circ_128675,RMVar_hsa_circ_40274,RMVar_hsa_circ_335395 67238 RMVar_ID_67238 Human_SNP_ID_1887472 m1A Human chr1 - 6678327 6678327 6678327 GTCATTAAACAGTTACAGAACATCTCCCCAAAACCCTGCAATCTGTAATATTGTCTTTGGGAATA GTCATTAAACAGTTACAGAACATCTCCCCAAAGCCCTGCAATCTGTAATATTGTCTTTGGGAATA T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6678325..6678537 26863196 MeRIP-seq:(Medium) rs1223934652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2161547,Human_RBP_ID_3320341 RMVar_hsa_circ_128678,RMVar_hsa_circ_287254 67239 RMVar_ID_67239 Human_SNP_ID_1893259 m1A Human chr1 + 6701683 6701683 6701683 GGCGGCCACCGCCAGCCCGGCCCTCCCGAACGACCGGGCTCGGCCTCAGCCCCCAGAGCGTCCAG GGCGGCCACCGCCAGCCCGGCCCTCCCGAACGTCCGGGCTCGGCCTCAGCCCCCAGAGCGTCCAG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:6701681..6701767 26863410 MeRIP-seq:(Medium) rs1273463968 Functional Loss SNV dbSNP153 33..33 33 - - - 67240 RMVar_ID_67240 Human_SNP_ID_1915814 m1A Human chr1 + 6784741 6784699 6784741 GACGCGGCGCCGAGGGGGCGGGGCCTGGCGGGAGGCTCGCCCCTCCCCCACGGCCGGCAGCGACG _________________________________GGCTCGCCCCTCCCCCACGGCCGGCAGCGACG GGGCCGTGGGGACGCGGCGCCGAGGGGGCGGGGCCTGGCGGGA G lnc-CAMTA1-3 RNACentral:URS00008B5F92 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:6784669..6784757 26863410 MeRIP-seq:(Medium) rs1321573598 Functional Loss DEL dbSNP153 1..33 33 - - - 67241 RMVar_ID_67241 Human_SNP_ID_1916150 m1A Human chr1 + 6785519 6785517 6785520 GTACGAGGCGCGCGCTCGGGGTCCCGGTCGCGAGGAGGAGGAGGATGTGGCGCGCGGAGGGGAAA GTACGAGGCGCGCGCTCGGGGTCCCGGTCGC___GAGGAGGAGGATGTGGCGCGCGGAGGGGAAA CGAG C CAMTA1 Ensembl:ENSG00000171735 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:6785476..6785638 26863196 MeRIP-seq:(Medium) rs755609750 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_102,Human_RBP_ID_25666,Human_RBP_ID_361162,Human_RBP_ID_4064475,Human_RBP_ID_5311514,Human_RBP_ID_5857363,Human_RBP_ID_8227944,Human_RBP_ID_8939936,Human_RBP_ID_9318545,Human_RBP_ID_18414840,Human_RBP_ID_22870728,Human_RBP_ID_26310137,Human_RBP_ID_26382766,Human_RBP_ID_27835084 Human_Splice_Rec_13279,Human_Splice_Rec_13283,Human_Splice_Rec_13327,Human_Splice_Rec_13333,Human_Splice_Rec_13339,Human_Splice_Rec_13345,Human_Splice_Rec_13351 67242 RMVar_ID_67242 Human_SNP_ID_1916153 m1A Human chr1 + 6785519 6785519 6785519 GTACGAGGCGCGCGCTCGGGGTCCCGGTCGCGAGGAGGAGGAGGATGTGGCGCGCGGAGGGGAAA GTACGAGGCGCGCGCTCGGGGTCCCGGTCGCGTGGAGGAGGAGGATGTGGCGCGCGGAGGGGAAA A T CAMTA1 Ensembl:ENSG00000171735 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:6785476..6785638 26863196 MeRIP-seq:(Medium) rs781157444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102,Human_RBP_ID_25666,Human_RBP_ID_361162,Human_RBP_ID_4064475,Human_RBP_ID_5311514,Human_RBP_ID_5857363,Human_RBP_ID_8227944,Human_RBP_ID_8939936,Human_RBP_ID_9318545,Human_RBP_ID_18414840,Human_RBP_ID_22870728,Human_RBP_ID_26310137,Human_RBP_ID_26382766,Human_RBP_ID_27835084 Human_Splice_Rec_13279,Human_Splice_Rec_13283,Human_Splice_Rec_13327,Human_Splice_Rec_13333,Human_Splice_Rec_13339,Human_Splice_Rec_13345,Human_Splice_Rec_13351 67243 RMVar_ID_67243 Human_SNP_ID_1916171 m1A Human chr1 + 6785564 6785564 6785564 TGTGGCGCGCGGAGGGGAAATGGCTGCCGAAAACAAGCCGGAAGGTAAGAGCCGGAGCGCGAGGG TGTGGCGCGCGGAGGGGAAATGGCTGCCGAAAGCAAGCCGGAAGGTAAGAGCCGGAGCGCGAGGG A G CAMTA1 Ensembl:ENSG00000171735 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:6785471..6785564 26863410 MeRIP-seq:(Medium) rs769546370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102,Human_RBP_ID_4073486,Human_RBP_ID_5311514,Human_RBP_ID_8227944,Human_RBP_ID_8939936,Human_RBP_ID_18414840,Human_RBP_ID_22870728,Human_RBP_ID_26310137 Human_Splice_Rec_13279,Human_Splice_Rec_13283,Human_Splice_Rec_13327,Human_Splice_Rec_13333,Human_Splice_Rec_13339,Human_Splice_Rec_13345,Human_Splice_Rec_13351 67244 RMVar_ID_67244 Human_SNP_ID_1921807 m1A Human chr1 + 6806945 6806945 6806945 CATTGGTTATTGTTATACTTTTAAGTCACTTCATTTACTCAACAAATAACAAAGTGCCTATCTGT CATTGGTTATTGTTATACTTTTAAGTCACTTCGTTTACTCAACAAATAACAAAGTGCCTATCTGT A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6806942..6807048 26863196 MeRIP-seq:(Medium) rs560032828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17757027 67245 RMVar_ID_67245 Human_SNP_ID_1922066 m1A Human chr1 + 6807976 6807976 6807976 ATGCTTTAATAAGGCTCTGGAAGGGAAGATGGAAAGACTTCCGGGAGGAGGTGGAATTTGACCTG ATGCTTTAATAAGGCTCTGGAAGGGAAGATGGGAAGACTTCCGGGAGGAGGTGGAATTTGACCTG A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6807973..6808181 26863196 MeRIP-seq:(Medium) rs1275206119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8317836 RMVar_hsa_circ_128681,RMVar_hsa_circ_86544,RMVar_hsa_circ_284180,RMVar_hsa_circ_128682,RMVar_hsa_circ_128680 67246 RMVar_ID_67246 Human_SNP_ID_1924846 m1A Human chr1 + 6820192 6820192 6820192 TTTTATTTTCTGTTTCCTTAGAGCGTTTCCCAAAGTGTATTCTGCGGAACTAGCACCTACTGTGT TTTTATTTTCTGTTTCCTTAGAGCGTTTCCCAGAGTGTATTCTGCGGAACTAGCACCTACTGTGT A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:6820176..6820275 26863196 MeRIP-seq:(Medium) rs1557624268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073487,Human_RBP_ID_8317850,Human_RBP_ID_17182120 Human_Splice_Rec_13284,Human_Splice_Rec_13285,Human_Splice_Rec_13334,Human_Splice_Rec_13335,Human_Splice_Rec_13340,Human_Splice_Rec_13341,Human_Splice_Rec_13352,Human_Splice_Rec_13353,Human_Splice_Rec_13360,Human_Splice_Rec_13361 RMVar_hsa_circ_64611,RMVar_hsa_circ_128681,RMVar_hsa_circ_86544,RMVar_hsa_circ_284180,RMVar_hsa_circ_128682,RMVar_hsa_circ_110317,RMVar_hsa_circ_128683,RMVar_hsa_circ_128680,RMVar_hsa_circ_296538,RMVar_hsa_circ_82278,RMVar_hsa_circ_128685,RMVar_hsa_circ_128686,RMVar_hsa_circ_128684 67247 RMVar_ID_67247 Human_SNP_ID_1929914 m1A Human chr1 - 6840751 6840751 6840751 TGTGCTGGCTCCTCCTGCACTGCTCGGGGCTTAGTCTCCCTTTCTCCATCTATCTTCTGCATCCC TGTGCTGGCTCCTCCTGCACTGCTCGGGGCTTGGTCTCCCTTTCTCCATCTATCTTCTGCATCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6840739..6840844 26863196 MeRIP-seq:(Medium) rs935861265 Functional Loss SNV dbSNP153 33..33 33 - - - 67248 RMVar_ID_67248 Human_SNP_ID_1929915 m1A Human chr1 - 6840751 6840751 6840751 TGTGCTGGCTCCTCCTGCACTGCTCGGGGCTTAGTCTCCCTTTCTCCATCTATCTTCTGCATCCC TGTGCTGGCTCCTCCTGCACTGCTCGGGGCTTCGTCTCCCTTTCTCCATCTATCTTCTGCATCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6840739..6840844 26863196 MeRIP-seq:(Medium) rs935861265 Functional Loss SNV dbSNP153 33..33 33 - - - 67249 RMVar_ID_67249 Human_SNP_ID_1930096 m1A Human chr1 + 6841622 6841622 6841622 AGGAAAGTAAATAGTGGCAAGAATTACAAAGGAAAAGCACAGAGGACAGCTCTGAGAGGATGAAA AGGAAAGTAAATAGTGGCAAGAATTACAAAGGTAAAGCACAGAGGACAGCTCTGAGAGGATGAAA A T CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6841620..6841748 26863196 MeRIP-seq:(Medium) rs1300119727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11089569 RMVar_hsa_circ_64611,RMVar_hsa_circ_128681,RMVar_hsa_circ_86544,RMVar_hsa_circ_128682,RMVar_hsa_circ_110317,RMVar_hsa_circ_128683,RMVar_hsa_circ_82278,RMVar_hsa_circ_61652,RMVar_hsa_circ_128685,RMVar_hsa_circ_128686 67250 RMVar_ID_67250 Human_SNP_ID_1931999 m1A Human chr1 + 6849345 6849345 6849345 TGTAGATTTGGGACCTAGAGAGAGCTCAAAGAAGCTGAGAGTACGGATAAAATTTTCCTTGGAGA TGTAGATTTGGGACCTAGAGAGAGCTCAAAGACGCTGAGAGTACGGATAAAATTTTCCTTGGAGA A C CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:6849338..6849616 26863196 MeRIP-seq:(Medium) rs1255967058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1434470,Human_RBP_ID_11089757 RMVar_hsa_circ_64611,RMVar_hsa_circ_128681,RMVar_hsa_circ_86544,RMVar_hsa_circ_128682,RMVar_hsa_circ_110317,RMVar_hsa_circ_128683,RMVar_hsa_circ_82278,RMVar_hsa_circ_61652,RMVar_hsa_circ_128685,RMVar_hsa_circ_128686 67251 RMVar_ID_67251 Human_SNP_ID_1949137 m1A Human chr1 + 6917140 6917140 6917140 TTGCCCTATAAAGAGATGGCATCCAGGGAGAGAGTGGCATGTTCATGACAGTGGAGGAAGCCAGA TTGCCCTATAAAGAGATGGCATCCAGGGAGAGCGTGGCATGTTCATGACAGTGGAGGAAGCCAGA A C CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6917116..6917420 26863196 MeRIP-seq:(Medium) rs1892261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8021,GWAS_ID_8022,GWAS_ID_8023,GWAS_ID_8024,GWAS_ID_8025 RMVar_hsa_circ_61652 67252 RMVar_ID_67252 Human_SNP_ID_1949138 m1A Human chr1 + 6917140 6917140 6917140 TTGCCCTATAAAGAGATGGCATCCAGGGAGAGAGTGGCATGTTCATGACAGTGGAGGAAGCCAGA TTGCCCTATAAAGAGATGGCATCCAGGGAGAGGGTGGCATGTTCATGACAGTGGAGGAAGCCAGA A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6917116..6917420 26863196 MeRIP-seq:(Medium) rs1892261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8021,GWAS_ID_8022,GWAS_ID_8023,GWAS_ID_8024,GWAS_ID_8025 RMVar_hsa_circ_61652 67253 RMVar_ID_67253 Human_SNP_ID_1949139 m1A Human chr1 + 6917140 6917140 6917140 TTGCCCTATAAAGAGATGGCATCCAGGGAGAGAGTGGCATGTTCATGACAGTGGAGGAAGCCAGA TTGCCCTATAAAGAGATGGCATCCAGGGAGAGTGTGGCATGTTCATGACAGTGGAGGAAGCCAGA A T CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6917116..6917420 26863196 MeRIP-seq:(Medium) rs1892261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8021,GWAS_ID_8022,GWAS_ID_8023,GWAS_ID_8024,GWAS_ID_8025 RMVar_hsa_circ_61652 67254 RMVar_ID_67254 Human_SNP_ID_1954321 m1A Human chr1 - 6937241 6937241 6937241 TGATGGTAGTGGTGATGATGATGGTGTTGGTGATGATAGTGGTGGTAAGTGGTGAATGATGATGG TGATGGTAGTGGTGATGATGATGGTGTTGGTGGTGATAGTGGTGGTAAGTGGTGAATGATGATGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6937231..6937301 26863196 MeRIP-seq:(Medium) rs1396369625 Functional Loss SNV dbSNP153 33..33 33 - - - 67255 RMVar_ID_67255 Human_SNP_ID_2050200 m1A Human chr1 - 7335158 7335144 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC______________CCCCCACACACACACACAC GGGGGGGGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537341 Functional Loss DEL dbSNP153 33..46 33 - - - 67256 RMVar_ID_67256 Human_SNP_ID_2050205 m1A Human chr1 - 7335158 7335146 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC____________CCCCCCCACACACACACACAC GGGGGGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537368 Functional Loss DEL dbSNP153 33..44 33 - - - 67257 RMVar_ID_67257 Human_SNP_ID_2050211 m1A Human chr1 - 7335158 7335148 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC__________CCCCCCCCCACACACACACACAC GGGGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537422 Functional Loss DEL dbSNP153 33..42 33 - - - 67258 RMVar_ID_67258 Human_SNP_ID_2050218 m1A Human chr1 - 7335158 7335150 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC________CCCCCCCCCCCACACACACACACAC GGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537473 Functional Loss DEL dbSNP153 33..40 33 - - - 67259 RMVar_ID_67259 Human_SNP_ID_2050221 m1A Human chr1 - 7335158 7335151 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC_______CCCCCCCCCCCCACACACACACACAC GGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537502 Functional Loss DEL dbSNP153 33..39 33 - - - 67260 RMVar_ID_67260 Human_SNP_ID_2050226 m1A Human chr1 - 7335158 7335153 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC_____CCCCCCCCCCCCCCACACACACACACAC GGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537541 Functional Loss DEL dbSNP153 33..37 33 - - - 67261 RMVar_ID_67261 Human_SNP_ID_2050227 m1A Human chr1 - 7335158 7335154 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC____CCCCCCCCCCCCCCCACACACACACACAC GGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537561 Functional Loss DEL dbSNP153 33..36 33 - - - 67262 RMVar_ID_67262 Human_SNP_ID_2050232 m1A Human chr1 - 7335158 7335156 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC__CCCCCCCCCCCCCCCCCACACACACACACAC GGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537586 Functional Loss DEL dbSNP153 33..34 33 - - - 67263 RMVar_ID_67263 Human_SNP_ID_2050234 m1A Human chr1 - 7335158 7335157 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCC_CCCCCCCCCCCCCCCCCCACACACACACACAC GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs1557537601 Functional Loss DEL dbSNP153 33..33 33 - - - 67264 RMVar_ID_67264 Human_SNP_ID_2050237 m1A Human chr1 - 7335158 7335158 7335158 GGTAGCCTCGGGGTCTGACACCCCCCACCCCCACCCCCCCCCCCCCCCCCCACACACACACACAC GGTAGCCTCGGGGTCTGACACCCCCCACCCCCCCCCCCCCCCCCCCCCCCCACACACACACACAC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7335126..7335175 26863196 MeRIP-seq:(Medium) rs958682403 Functional Loss SNV dbSNP153 33..33 33 - - - 67265 RMVar_ID_67265 Human_SNP_ID_2056973 m1A Human chr1 + 7362506 7362506 7362506 AGTGGACTGGTGGAATTTAATAGAGTTGGTAGACTTGGGTAGAGGTGGTGGACATGGGTACCGAT AGTGGACTGGTGGAATTTAATAGAGTTGGTAGGCTTGGGTAGAGGTGGTGGACATGGGTACCGAT A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7362501..7362765 26863196 MeRIP-seq:(Medium) rs1274428440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26072 67266 RMVar_ID_67266 Human_SNP_ID_2077643 m1A Human chr1 - 7445089 7445089 7445089 CACCTCCCCTTGAGGCACCCCTCCCACCTCCCACCTGAGGCACAGAGGTAACCCCCACCCCATCC CACCTCCCCTTGAGGCACCCCTCCCACCTCCCCCCTGAGGCACAGAGGTAACCCCCACCCCATCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7445076..7445125 26863196 MeRIP-seq:(Medium) rs1203446725 Functional Loss SNV dbSNP153 33..33 33 - - - 67267 RMVar_ID_67267 Human_SNP_ID_2082349 m1A Human chr1 + 7463331 7463330 7463332 CAGACACAGAGACAGGGACAGGCAAGGGAAACAGAGACAGGGAGAGACAGAGAGACAGAGAAAGA CAGACACAGAGACAGGGACAGGCAAGGGAAAC__AGACAGGGAGAGACAGAGAGACAGAGAAAGA CAG C CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7463298..7463363 26863196 MeRIP-seq:(Medium) rs1297541157 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_26072 67268 RMVar_ID_67268 Human_SNP_ID_2092120 m1A Human chr1 - 7498400 7498400 7498400 ACGCACATCCACACACTCATACACACTCATACACATTCACTCACACACATCCACTCATACACACA ACGCACATCCACACACTCATACACACTCATACTCATTCACTCACACACATCCACTCATACACACA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:7498352..7498423 26863196 MeRIP-seq:(Medium) rs958852960 Functional Loss SNV dbSNP153 33..33 33 - - - 67269 RMVar_ID_67269 Human_SNP_ID_2092979 m1A Human chr1 + 7499621 7499618 7499622 AGTGCGTATGTATATGAGTGTGTGTGTGCATGAGTGAGTGTGAGCCTGGTGTGAGTGCATGTGTA AGTGCGTATGTATATGAGTGTGTGTGTGCA____TGAGTGTGAGCCTGGTGTGAGTGCATGTGTA ATGAG A CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7499571..7499754 26863196 MeRIP-seq:(Medium) rs141443382 Functional Loss DEL dbSNP153 31..34 33 - - - 67270 RMVar_ID_67270 Human_SNP_ID_2093448 m1A Human chr1 - 7500323 7500319 7500323 CGCACACCAGGCTCACACCATCCTCTCTACACACTCGCTCACGGACACACATGCACACACACACT CGCACACCAGGCTCACACCATCCTCTCTACAC____GCTCACGGACACACATGCACACACACACT CGAGT C lnc-UTS2-10 RNACentral:URS00008B4628 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7500290..7500397 26863196 MeRIP-seq:(Medium) rs1475899029 Functional Loss DEL dbSNP153 33..36 33 - - - 67271 RMVar_ID_67271 Human_SNP_ID_2093450 m1A Human chr1 - 7500323 7500323 7500323 CGCACACCAGGCTCACACCATCCTCTCTACACACTCGCTCACGGACACACATGCACACACACACT CGCACACCAGGCTCACACCATCCTCTCTACACCCTCGCTCACGGACACACATGCACACACACACT T G lnc-UTS2-10 RNACentral:URS00008B4628 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7500290..7500397 26863196 MeRIP-seq:(Medium) rs1162155692 Functional Loss SNV dbSNP153 33..33 33 - - - 67272 RMVar_ID_67272 Human_SNP_ID_2130540 m1A Human chr1 - 7646114 7646075 7646115 CATCCACCTCAACGGGGCCTCCGCTCACACTTACCAGGGCCTCCACCCAACTCACCATGGCCTCC CATCCACCTCAACGGGGCCTCCGCTCACACTCACCAGGACCTCCTCCCAACCCACCAGAGCCTCC ATTGGGTGGAGGCCATGGTGAGTTGGGTGGAGGCCCTGGTA GTTGGGTGGAGGCTCTGGTGGGTTGGGAGGAGGTCCTGGTG - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:7646058..7646168;chr1:7646064..7646188 26863196 MeRIP-seq:(Medium) rs386628203 Functional Loss MNV dbSNP153 32..65 33 - - - 67273 RMVar_ID_67273 Human_SNP_ID_2130607 m1A Human chr1 + 7646212 7646212 7646212 GACTGTGAGGGTGGAGGCCATGGTGATTGTGAAGGTGGAGGCTATGGTGAGTTGGGTGGAGGCCC GACTGTGAGGGTGGAGGCCATGGTGATTGTGAGGGTGGAGGCTATGGTGAGTTGGGTGGAGGCCC A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7646021..7646722 26863196 MeRIP-seq:(Medium) rs1271708334 Functional Loss SNV dbSNP153 33..33 33 - - - 67274 RMVar_ID_67274 Human_SNP_ID_2146996 m1A Human chr1 - 7704882 7704882 7704882 CCGCGCCGCCGCGCACCTACCCGGACCTGCTGAGCTCGGCTCCTGCTCGTCAGGCTTGCGCCGAG CCGCGCCGCCGCGCACCTACCCGGACCTGCTGTGCTCGGCTCCTGCTCGTCAGGCTTGCGCCGAG T A lnc-UTS2-5 RNACentral:URS00008B6A17 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:7704785..7704922 26863196 MeRIP-seq:(Medium) rs1336117605 Functional Loss SNV dbSNP153 33..33 33 - - - 67275 RMVar_ID_67275 Human_SNP_ID_2167280 m1A Human chr1 - 7784670 7784670 7784670 CTCCAACATTTTCAAAACCCGGAGCTCGCTCGACTTTCAGGACTCCGGCCTAGGGGGAGGAGACA CTCCAACATTTTCAAAACCCGGAGCTCGCTCGGCTTTCAGGACTCCGGCCTAGGGGGAGGAGACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:7784662..7784744 26863196 MeRIP-seq:(Medium) rs927711128 Functional Loss SNV dbSNP153 33..33 33 - - - 67276 RMVar_ID_67276 Human_SNP_ID_2170590 m1A Human chr1 + 7795563 7795563 7795563 GGCAAGTGTCTGAGAAAGTGTGTTCCAGGCAGAGGGAGCAGCAGGCGCAGAGGCCCTGGGGTGGG GGCAAGTGTCTGAGAAAGTGTGTTCCAGGCAGGGGGAGCAGCAGGCGCAGAGGCCCTGGGGTGGG A G PER3 Ensembl:ENSG00000049246 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:7795514..7795660 26863196 MeRIP-seq:(Medium) rs1010512102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61504,RMVar_hsa_circ_8465,RMVar_hsa_circ_58378,RMVar_hsa_circ_366402,RMVar_hsa_circ_48892,RMVar_hsa_circ_7970,RMVar_hsa_circ_128701,RMVar_hsa_circ_316675,RMVar_hsa_circ_377272 67277 RMVar_ID_67277 Human_SNP_ID_2179001 m1A Human chr1 - 7827284 7827284 7827284 GCAGGTGGGAAGGTCGGGCTCGAGGTGTGCGGAGAGGAGGCCGCGGAGGGGCAGCAGGGCTGTGC GCAGGTGGGAAGGTCGGGCTCGAGGTGTGCGGCGAGGAGGCCGCGGAGGGGCAGCAGGGCTGTGC T G Z98884.1 Ensembl:ENSG00000236266 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7827234..7827338 26863196 MeRIP-seq:(Medium) rs146211083 Functional Loss SNV dbSNP153 33..33 33 - - - 67278 RMVar_ID_67278 Human_SNP_ID_2179056 m1A Human chr1 + 7827368 7827368 7827368 GCCCCTTACCTCGTCCCAGCTTTTCCCCTCCCAGCCGCGACCTCACCCGGAAGAGAATACGCAGC GCCCCTTACCTCGTCCCAGCTTTTCCCCTCCCCGCCGCGACCTCACCCGGAAGAGAATACGCAGC A C PER3 Ensembl:ENSG00000049246 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:7827319..7827450 26863196 MeRIP-seq:(Medium) rs1413160426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364913,RMVar_hsa_circ_318730,RMVar_hsa_circ_359818,RMVar_hsa_circ_56979 67279 RMVar_ID_67279 Human_SNP_ID_2179057 m1A Human chr1 + 7827368 7827368 7827368 GCCCCTTACCTCGTCCCAGCTTTTCCCCTCCCAGCCGCGACCTCACCCGGAAGAGAATACGCAGC GCCCCTTACCTCGTCCCAGCTTTTCCCCTCCCTGCCGCGACCTCACCCGGAAGAGAATACGCAGC A T PER3 Ensembl:ENSG00000049246 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:7827319..7827450 26863196 MeRIP-seq:(Medium) rs1413160426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364913,RMVar_hsa_circ_318730,RMVar_hsa_circ_359818,RMVar_hsa_circ_56979 67280 RMVar_ID_67280 Human_SNP_ID_2202496 m1A Human chr1 - 7914255 7914255 7914255 AGGGGAGGGAGGGATGGAGTTGGGGGACGGGGAGGGGGAAGGGGGAGGGAAGGGGGCGGGGGAGG AGGGGAGGGAGGGATGGAGTTGGGGGACGGGGGGGGGGAAGGGGGAGGGAAGGGGGCGGGGGAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:7914205..7914332 26863196 MeRIP-seq:(Medium) rs1274577001 Functional Loss SNV dbSNP153 33..33 33 - - - 67281 RMVar_ID_67281 Human_SNP_ID_2214937 m1A Human chr1 - 7961737 7961737 7961737 GACGCGGCGCCCCGGCCCGTTGGGTACCACTCACCCCACACCAGGCTGAAAATGAACGCACGCCA GACGCGGCGCCCCGGCCCGTTGGGTACCACTCTCCCCACACCAGGCTGAAAATGAACGCACGCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:7961651..7961930;chr1:7961676..7961885;chr1:7961651..7962029;chr1:7961729..7961930;chr1:7961701..7961930 26863196,32194978,32194978 MeRIP-seq:(Medium) rs140230911 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_270 67282 RMVar_ID_67282 Human_SNP_ID_2214960 m1A Human chr1 + 7961792 7961792 7961792 GCGCCGCGTCCGCAGGAAGAGGCGCGGGGTGCAGGTCAGCGCCAGCGGGGGCGCGGCGCATGTGT GCGCCGCGTCCGCAGGAAGAGGCGCGGGGTGCCGGTCAGCGCCAGCGGGGGCGCGGCGCATGTGT A C PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:7961676..7961930 26863410 MeRIP-seq:(Medium) rs988806431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803680,Human_RBP_ID_4073496,Human_RBP_ID_5312297,Human_RBP_ID_5336815,Human_RBP_ID_19036541 Human_Splice_Rec_13773,Human_Splice_Rec_13785 RMVar_hsa_circ_122172,RMVar_hsa_circ_128706 67283 RMVar_ID_67283 Human_SNP_ID_2215308 m1A Human chr1 - 7962814 7962814 7962814 TGACCGTCTCCATTTCCTCTGCTCCTTTAGCCAGGATGACCAGAGCTCTTTTGGAAGCCATTTTT TGACCGTCTCCATTTCCTCTGCTCCTTTAGCCGGGATGACCAGAGCTCTTTTGGAAGCCATTTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7962723..7962919 26863196 MeRIP-seq:(Medium) rs1553122735 Functional Loss SNV dbSNP153 33..33 33 - - - 67284 RMVar_ID_67284 Human_SNP_ID_2222136 m1A Human chr1 + 7986713 7986713 7986713 AGCAGGAGCAGGGAGTGTAGAGGCCCTGCCGCAGGAGCATTGAGAGGCGGGTTAGAGAAACATGG AGCAGGAGCAGGGAGTGTAGAGGCCCTGCCGCGGGAGCATTGAGAGGCGGGTTAGAGAAACATGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:7986662..7986747 26863196 MeRIP-seq:(Medium) rs887712960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128712 67285 RMVar_ID_67285 Human_SNP_ID_2223105 m1A Human chr1 + 7990335 7990315 7990336 TCATTACCACCAGCATCACCCTCACCACCATCACCATCACCACCACCATCACCTTCACCACCACC TCATTACCACCAG_____________________CATCACCACCACCATCACCTTCACCACCACC GCATCACCCTCACCACCATCAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7990317..7990468 26863196 MeRIP-seq:(Medium) rs969588810 Functional Loss DEL dbSNP153 14..34 33 - - - RMVar_hsa_circ_128712 67286 RMVar_ID_67286 Human_SNP_ID_2223117 m1A Human chr1 + 7990335 7990333 7990336 TCATTACCACCAGCATCACCCTCACCACCATCACCATCACCACCACCATCACCTTCACCACCACC TCATTACCACCAGCATCACCCTCACCACCAT___CATCACCACCACCATCACCTTCACCACCACC TCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:7990317..7990468 26863196 MeRIP-seq:(Medium) rs1557455564 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_128712 67287 RMVar_ID_67287 Human_SNP_ID_2232406 m1A Human chr1 - 8026258 8026258 8026258 GCAGAGTGCTAGCGGGAGCGCGAGCCAGCAAGAGGCGCCTGCGCGATGTCCGGGCCCCTGAGCCC GCAGAGTGCTAGCGGGAGCGCGAGCCAGCAAGGGGCGCCTGCGCGATGTCCGGGCCCCTGAGCCC T C ERRFI1 Ensembl:ENSG00000116285 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:8026132..8026291;chr1:8015593..8026285 26863196 MeRIP-seq:(Medium) rs897323336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072484,Human_RBP_ID_22534819 67288 RMVar_ID_67288 Human_SNP_ID_2232407 m1A Human chr1 - 8026260 8026260 8026260 AGGCAGAGTGCTAGCGGGAGCGCGAGCCAGCAAGAGGCGCCTGCGCGATGTCCGGGCCCCTGAGC AGGCAGAGTGCTAGCGGGAGCGCGAGCCAGCAGGAGGCGCCTGCGCGATGTCCGGGCCCCTGAGC T C ERRFI1 Ensembl:ENSG00000116285 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8026013..8026300 26863196 MeRIP-seq:(Medium) rs1297114940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744631,Human_RBP_ID_4072484,Human_RBP_ID_22534819 67289 RMVar_ID_67289 Human_SNP_ID_2232423 m1A Human chr1 - 8026274 8026274 8026274 GGCGGTCCGGTGCGAGGCAGAGTGCTAGCGGGAGCGCGAGCCAGCAAGAGGCGCCTGCGCGATGT GGCGGTCCGGTGCGAGGCAGAGTGCTAGCGGGGGCGCGAGCCAGCAAGAGGCGCCTGCGCGATGT T C ERRFI1 Ensembl:ENSG00000116285 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr1:8026188..8026273;chr1:8026044..8026293 26863410,26863196 MeRIP-seq:(Medium) rs988103916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744631,Human_RBP_ID_4072484,Human_RBP_ID_22534819 67290 RMVar_ID_67290 Human_SNP_ID_2232744 m1A Human chr1 - 8026937 8026937 8026937 ACACAGTCCCTCACTGTCCCTCATCGTCCCGCACTGTCCCTCACCGTCCCACACCGTCTCTCATC ACACAGTCCCTCACTGTCCCTCATCGTCCCGCGCTGTCCCTCACCGTCCCACACCGTCTCTCATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8026886..8027167 26863196 MeRIP-seq:(Medium) rs1450131557 Functional Loss SNV dbSNP153 33..33 33 - - - 67291 RMVar_ID_67291 Human_SNP_ID_2232751 m1A Human chr1 + 8026943 8026943 8026943 AGACGGTGTGGGACGGTGAGGGACAGTGCGGGACGATGAGGGACAGTGAGGGACTGTGTAGGACA AGACGGTGTGGGACGGTGAGGGACAGTGCGGGGCGATGAGGGACAGTGAGGGACTGTGTAGGACA A G AL034417.3 Ensembl:ENSG00000238290 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:8026899..8027288 26863196 MeRIP-seq:(Medium) rs1224193058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801398,Human_RBP_ID_8171357,Human_RBP_ID_26773980 67292 RMVar_ID_67292 Human_SNP_ID_2319127 m1A Human chr1 + 8353141 8353141 8353141 GGAAACGAATGCCTTCAAGCCAATGTGGCCTGAAGTCCCACGACAAAAGGTTCATGTCAGCTTTG GGAAACGAATGCCTTCAAGCCAATGTGGCCTGGAGTCCCACGACAAAAGGTTCATGTCAGCTTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:8353090..8354991 32194978 MeRIP-seq:(Medium) rs974763689 Functional Loss SNV dbSNP153 33..33 33 - - - 67293 RMVar_ID_67293 Human_SNP_ID_2320894 m1A Human chr1 + 8358567 8358567 8358567 GCTCTGGGGGCTTCACCTCGAAGCCCGGCTTCATCCTCTCCCGCAGCTCCCGCTCTCGGATCTCC GCTCTGGGGGCTTCACCTCGAAGCCCGGCTTCTTCCTCTCCCGCAGCTCCCGCTCTCGGATCTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8355532..8359925 26863196 MeRIP-seq:(Medium) rs1473558561 Functional Loss SNV dbSNP153 33..33 33 - - - 67294 RMVar_ID_67294 Human_SNP_ID_2321557 m1A Human chr1 - 8359898 8359898 8359898 TCATGCCTCTGGCCGGGTCCAAGCTGGCCAAGAAGAGGGAGGAGGCCATTGAGAAGGCCAAGCGC TCATGCCTCTGGCCGGGTCCAAGCTGGCCAAGGAGAGGGAGGAGGCCATTGAGAAGGCCAAGCGC T C RERE Ensembl:ENSG00000142599 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:8359848..8359948 32194978 MeRIP-seq:(Medium) rs769621779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18187480,Human_RBP_ID_22557654,Human_RBP_ID_22786337 Human_Splice_Rec_13972,Human_Splice_Rec_14016,Human_Splice_Rec_14048,Human_Splice_Rec_14102 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_116183,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128718,RMVar_hsa_circ_128716 67295 RMVar_ID_67295 Human_SNP_ID_2321691 m1A Human chr1 + 8360183 8360183 8360183 GTGGGCTCCGGGGACGGGCTCCTTGGTGGGGGAGGGGGGCTCTCAGGCTCCTCAGCGTCGTCCAG GTGGGCTCCGGGGACGGGCTCCTTGGTGGGGGTGGGGGGCTCTCAGGCTCCTCAGCGTCGTCCAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8360132..8360320 26863196 MeRIP-seq:(Medium) rs1225958615 Functional Loss SNV dbSNP153 33..33 33 - - - 67296 RMVar_ID_67296 Human_SNP_ID_2321954 m1A Human chr1 - 8360629 8360629 8360629 CCCACCTCTCGGGGCCCTCACCCTTCTCCATGAATGCCAACCTGCCTCCCCCTCCAGCCCTGAAG CCCACCTCTCGGGGCCCTCACCCTTCTCCATGGATGCCAACCTGCCTCCCCCTCCAGCCCTGAAG T C RERE Ensembl:ENSG00000142599 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:8360579..8360746 26863196 MeRIP-seq:(Medium) rs1383276634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1257619,Human_RBP_ID_3329938,Human_RBP_ID_5125132,Human_RBP_ID_17070986,Human_RBP_ID_18927904 Human_miRNA_ID_2473824,Human_miRNA_ID_2473825,Human_miRNA_ID_2959610,Human_miRNA_ID_2959611 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128716 67297 RMVar_ID_67297 Human_SNP_ID_2321989 m1A Human chr1 - 8360707 8360707 8360707 TGGCCATGCCCCACATCAAGCCCCCGCCTACCACTCCCATCCCCCAGCTGCCGGCGCCACAGGCC TGGCCATGCCCCACATCAAGCCCCCGCCTACCCCTCCCATCCCCCAGCTGCCGGCGCCACAGGCC T G RERE Ensembl:ENSG00000142599 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8360497..8360829 26863196 MeRIP-seq:(Medium) rs1168686058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125133,Human_RBP_ID_17070987,Human_RBP_ID_17337933,Human_RBP_ID_18929204 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128716 67298 RMVar_ID_67298 Human_SNP_ID_2322142 m1A Human chr1 + 8361046 8361034 8361046 CCCAGTCAGAGGCTGCAGCGGGGGATGTGGCGAGGGATGCGGCGGGGGATGCGGTGAGGGCGGCC CCCAGTCAGAGGCTGCAGCGG____________GGGATGCGGCGGGGGATGCGGTGAGGGCGGCC GGGGATGTGGCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8360996..8361245 26863196 MeRIP-seq:(Medium) rs1435627210 Functional Loss DEL dbSNP153 22..33 33 - - - 67299 RMVar_ID_67299 Human_SNP_ID_2322154 m1A Human chr1 + 8361046 8361043 8361046 CCCAGTCAGAGGCTGCAGCGGGGGATGTGGCGAGGGATGCGGCGGGGGATGCGGTGAGGGCGGCC CCCAGTCAGAGGCTGCAGCGGGGGATGTGG___GGGATGCGGCGGGGGATGCGGTGAGGGCGGCC GCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8360996..8361245 26863196 MeRIP-seq:(Medium) rs1423069272 Functional Loss DEL dbSNP153 31..33 33 - - - 67300 RMVar_ID_67300 Human_SNP_ID_2322158 m1A Human chr1 + 8361046 8361046 8361046 CCCAGTCAGAGGCTGCAGCGGGGGATGTGGCGAGGGATGCGGCGGGGGATGCGGTGAGGGCGGCC CCCAGTCAGAGGCTGCAGCGGGGGATGTGGCGGGGGATGCGGCGGGGGATGCGGTGAGGGCGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8360996..8361245 26863196 MeRIP-seq:(Medium) rs897627996 Functional Loss SNV dbSNP153 33..33 33 - - - 67301 RMVar_ID_67301 Human_SNP_ID_2322787 m1A Human chr1 - 8362771 8362771 8362771 CCCTGATGGTCGCACCTCACCCATCAATGAAGACATCCGCTCCAGCGGCCGGAACTCCCCCAGCG CCCTGATGGTCGCACCTCACCCATCAATGAAGGCATCCGCTCCAGCGGCCGGAACTCCCCCAGCG T C RERE Ensembl:ENSG00000142599 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:8362720..8362821 26863196 MeRIP-seq:(Medium) rs748305572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9355428,Human_RBP_ID_17758678 Human_Splice_Rec_13966,Human_Splice_Rec_13967,Human_Splice_Rec_14010,Human_Splice_Rec_14011,Human_Splice_Rec_14042,Human_Splice_Rec_14043,Human_Splice_Rec_14096,Human_Splice_Rec_14097,Human_Splice_Rec_14111,Human_Splice_Rec_14150,Human_Splice_Rec_14151 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128716,RMVar_hsa_circ_335312 67302 RMVar_ID_67302 Human_SNP_ID_2366369 m1A Human chr1 - 8527783 8527783 8527783 GCTGGGGTACGCTGCCCCTGAGGGGTAACAAGAGAAAGGGCTGTCTGTCTTGGTGGCATGGCATG GCTGGGGTACGCTGCCCCTGAGGGGTAACAAGGGAAAGGGCTGTCTGTCTTGGTGGCATGGCATG T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8527780..8527955 26863196 MeRIP-seq:(Medium) rs1213382424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11122910,Human_RBP_ID_23416409 RMVar_hsa_circ_8704,RMVar_hsa_circ_52274,RMVar_hsa_circ_59089,RMVar_hsa_circ_271775,RMVar_hsa_circ_305113,RMVar_hsa_circ_296079,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_296431,RMVar_hsa_circ_285807,RMVar_hsa_circ_289805,RMVar_hsa_circ_281245,RMVar_hsa_circ_274528,RMVar_hsa_circ_309733,RMVar_hsa_circ_349230,RMVar_hsa_circ_278025,RMVar_hsa_circ_270778,RMVar_hsa_circ_49926,RMVar_hsa_circ_305891,RMVar_hsa_circ_339816,RMVar_hsa_circ_291499,RMVar_hsa_circ_128727,RMVar_hsa_circ_128729,RMVar_hsa_circ_277627,RMVar_hsa_circ_313286,RMVar_hsa_circ_370337,RMVar_hsa_circ_291989,RMVar_hsa_circ_271057,RMVar_hsa_circ_128728,RMVar_hsa_circ_128731,RMVar_hsa_circ_128726,RMVar_hsa_circ_128730 67303 RMVar_ID_67303 Human_SNP_ID_2388237 m1A Human chr1 + 8613440 8613440 8613440 GCTTATAAGGACAGGCTGCCATGTACACCTGGAAGGCTCCTACACTCTGCCTATCCACTTCTTAT GCTTATAAGGACAGGCTGCCATGTACACCTGGCAGGCTCCTACACTCTGCCTATCCACTTCTTAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8613436..8613529 26863196 MeRIP-seq:(Medium) rs773632452 Functional Loss SNV dbSNP153 33..33 33 - - - 67304 RMVar_ID_67304 Human_SNP_ID_2392971 m1A Human chr1 - 8634158 8634158 8634158 GGAAGAGCGGTTGTAGTAGCAGCAGCGTGAGGATGGGCATGGCTTGGTCTTGATTGAATGTGTCT GGAAGAGCGGTTGTAGTAGCAGCAGCGTGAGGGTGGGCATGGCTTGGTCTTGATTGAATGTGTCT T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8634153..8634266 26863196 MeRIP-seq:(Medium) rs768245991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59089,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_349230,RMVar_hsa_circ_49926,RMVar_hsa_circ_101600,RMVar_hsa_circ_313286,RMVar_hsa_circ_293781,RMVar_hsa_circ_42946,RMVar_hsa_circ_128744,RMVar_hsa_circ_308785,RMVar_hsa_circ_128732,RMVar_hsa_circ_304363,RMVar_hsa_circ_128749,RMVar_hsa_circ_128747,RMVar_hsa_circ_299449,RMVar_hsa_circ_371357,RMVar_hsa_circ_128750 67305 RMVar_ID_67305 Human_SNP_ID_2400410 m1A Human chr1 - 8663793 8663793 8663793 GAGGAGCATGCAGGAGGGGTGGAGGTGGAAGCAGTAGGGGAGAGGTGAGGCTGGAGAGGTGAAGG GAGGAGCATGCAGGAGGGGTGGAGGTGGAAGCTGTAGGGGAGAGGTGAGGCTGGAGAGGTGAAGG T A RERE Ensembl:ENSG00000142599 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8663792..8663947 26863196 MeRIP-seq:(Medium) rs900586364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5873248,Human_RBP_ID_21961162 RMVar_hsa_circ_49926,RMVar_hsa_circ_101600,RMVar_hsa_circ_42946,RMVar_hsa_circ_128732,RMVar_hsa_circ_371357,RMVar_hsa_circ_128750,RMVar_hsa_circ_334508 67306 RMVar_ID_67306 Human_SNP_ID_2418965 m1A Human chr1 + 8738097 8738097 8738097 CATGACCCCGCTGTGGGACTGGGCTGTCAAGCACTCTCCCTCCTCTGCTAACGCTGTTGCCTCTG CATGACCCCGCTGTGGGACTGGGCTGTCAAGCGCTCTCCCTCCTCTGCTAACGCTGTTGCCTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8738091..8738256 26863196 MeRIP-seq:(Medium) rs1303185322 Functional Loss SNV dbSNP153 33..33 33 - - - 67307 RMVar_ID_67307 Human_SNP_ID_2430368 m1A Human chr1 - 8784141 8784141 8784141 TCAGTGGAAAGGTCCTGAAGTGGGCACAAGGAAGACAGCGTGGTGGGAGCAGAATGAGCAGGGGG TCAGTGGAAAGGTCCTGAAGTGGGCACAAGGAGGACAGCGTGGTGGGAGCAGAATGAGCAGGGGG T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8784139..8784318 26863196 MeRIP-seq:(Medium) rs1210759007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8939937,Human_RBP_ID_23263141 RMVar_hsa_circ_49926,RMVar_hsa_circ_101600,RMVar_hsa_circ_42946,RMVar_hsa_circ_128732,RMVar_hsa_circ_371357,RMVar_hsa_circ_128750,RMVar_hsa_circ_334508 67308 RMVar_ID_67308 Human_SNP_ID_2439009 m1A Human chr1 + 8817478 8817478 8817478 CTGAGGATGATGGTGATTTTTTTTTTTTTTTAATCCTCAACTAGGAGAGAAAATGAGGCAGAGAC CTGAGGATGATGGTGATTTTTTTTTTTTTTTATTCCTCAACTAGGAGAGAAAATGAGGCAGAGAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8817427..8817633 26863196 MeRIP-seq:(Medium) rs1419535476 Functional Loss SNV dbSNP153 33..33 33 - - - 67309 RMVar_ID_67309 Human_SNP_ID_2439027 m1A Human chr1 + 8817528 8817528 8817528 AAATGAGGCAGAGACAATGTGGGGAGCGAGAGAGGGGAAAAGGACGGGGGAGGAGGCGGGGACCG AAATGAGGCAGAGACAATGTGGGGAGCGAGAGGGGGGAAAAGGACGGGGGAGGAGGCGGGGACCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:8817401..8817650 26863196 MeRIP-seq:(Medium) rs1325138001 Functional Loss SNV dbSNP153 33..33 33 - - - 67310 RMVar_ID_67310 Human_SNP_ID_2439035 m1A Human chr1 + 8817549 8817549 8817549 GGGAGCGAGAGAGGGGAAAAGGACGGGGGAGGAGGCGGGGACCGAGGCCCAGCGGGGCGAGCGTC GGGAGCGAGAGAGGGGAAAAGGACGGGGGAGGGGGCGGGGACCGAGGCCCAGCGGGGCGAGCGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:8817469..8817641 26863196 MeRIP-seq:(Medium) rs1431528726 Functional Loss SNV dbSNP153 33..33 33 - - - 67311 RMVar_ID_67311 Human_SNP_ID_2439081 m1A Human chr1 - 8817625 8817625 8817625 GGTGCCGCTGTTCCCACAGACGCTCGCGAGCAACCCTCCGCGCTCCGGAGCCTCCTCAGCCTCCC GGTGCCGCTGTTCCCACAGACGCTCGCGAGCAGCCCTCCGCGCTCCGGAGCCTCCTCAGCCTCCC T C RERE Ensembl:ENSG00000142599 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:8817526..8817625 26863410 MeRIP-seq:(Medium) rs1243026566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101600,RMVar_hsa_circ_128732 67312 RMVar_ID_67312 Human_SNP_ID_2450417 m1A Human chr1 - 8861320 8861320 8861320 GCAGGCAAGCCCTTCGGTCACCTGTTGGCTACACAGACCCCTCCCCTCGTGTCAGCTCAGGCAGC GCAGGCAAGCCCTTCGGTCACCTGTTGGCTACTCAGACCCCTCCCCTCGTGTCAGCTCAGGCAGC T A ENO1 Ensembl:ENSG00000074800 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:8861124..8861355 26863196 MeRIP-seq:(Medium) rs754420950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221152,Human_RBP_ID_364572,Human_RBP_ID_980280,Human_RBP_ID_1075683,Human_RBP_ID_1156281,Human_RBP_ID_1349999,Human_RBP_ID_1436305,Human_RBP_ID_1755809,Human_RBP_ID_3324606,Human_RBP_ID_4099651,Human_RBP_ID_5876581,Human_RBP_ID_8320934,Human_RBP_ID_8752597,Human_RBP_ID_9269325,Human_RBP_ID_11137595,Human_RBP_ID_17220394,Human_RBP_ID_17337511,Human_RBP_ID_17455518,Human_RBP_ID_17646095,Human_RBP_ID_18175010,Human_RBP_ID_18186785,Human_RBP_ID_18582405,Human_RBP_ID_19154803,Human_RBP_ID_22426836,Human_RBP_ID_22488887,Human_RBP_ID_22786409,Human_RBP_ID_26391251,Human_RBP_ID_27153453,Human_RBP_ID_27187231,Human_RBP_ID_27401418 Human_miRNA_ID_2152638,Human_miRNA_ID_2152639,Human_miRNA_ID_2800508,Human_miRNA_ID_2800509,Human_miRNA_ID_3008636,Human_miRNA_ID_3008637 RMVar_hsa_circ_111730,RMVar_hsa_circ_125498,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_82100,RMVar_hsa_circ_96254,RMVar_hsa_circ_110519,RMVar_hsa_circ_87544,RMVar_hsa_circ_128759,RMVar_hsa_circ_75856,RMVar_hsa_circ_81903,RMVar_hsa_circ_128761,RMVar_hsa_circ_128762,RMVar_hsa_circ_128760,RMVar_hsa_circ_128757,RMVar_hsa_circ_128758,RMVar_hsa_circ_128756,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752,RMVar_hsa_circ_268267 67313 RMVar_ID_67313 Human_SNP_ID_2450419 m1A Human chr1 - 8861322 8861322 8861322 GGGCAGGCAAGCCCTTCGGTCACCTGTTGGCTACACAGACCCCTCCCCTCGTGTCAGCTCAGGCA GGGCAGGCAAGCCCTTCGGTCACCTGTTGGCTGCACAGACCCCTCCCCTCGTGTCAGCTCAGGCA T C ENO1 Ensembl:ENSG00000074800 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:8861022..8861403 26863196 MeRIP-seq:(Medium) rs778409470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221152,Human_RBP_ID_364572,Human_RBP_ID_980281,Human_RBP_ID_1156282,Human_RBP_ID_1349999,Human_RBP_ID_1436305,Human_RBP_ID_1755810,Human_RBP_ID_2170786,Human_RBP_ID_3324607,Human_RBP_ID_4099651,Human_RBP_ID_5876581,Human_RBP_ID_8320934,Human_RBP_ID_8752597,Human_RBP_ID_9269325,Human_RBP_ID_11137595,Human_RBP_ID_17220395,Human_RBP_ID_17337512,Human_RBP_ID_17455518,Human_RBP_ID_17646095,Human_RBP_ID_18186785,Human_RBP_ID_18204891,Human_RBP_ID_18582405,Human_RBP_ID_22426836,Human_RBP_ID_22488887,Human_RBP_ID_22786409,Human_RBP_ID_26391251,Human_RBP_ID_26870976,Human_RBP_ID_27153453,Human_RBP_ID_27187231,Human_RBP_ID_27401418 Human_miRNA_ID_2152638,Human_miRNA_ID_2152639,Human_miRNA_ID_2667392,Human_miRNA_ID_2667393,Human_miRNA_ID_2800508,Human_miRNA_ID_2800509,Human_miRNA_ID_3008636,Human_miRNA_ID_3008637 RMVar_hsa_circ_111730,RMVar_hsa_circ_125498,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_82100,RMVar_hsa_circ_96254,RMVar_hsa_circ_110519,RMVar_hsa_circ_87544,RMVar_hsa_circ_128759,RMVar_hsa_circ_75856,RMVar_hsa_circ_81903,RMVar_hsa_circ_128761,RMVar_hsa_circ_128762,RMVar_hsa_circ_128760,RMVar_hsa_circ_128757,RMVar_hsa_circ_128758,RMVar_hsa_circ_128756,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752,RMVar_hsa_circ_268267 67314 RMVar_ID_67314 Human_SNP_ID_2450430 m1A Human chr1 - 8861346 8861346 8861346 AAACCCCTTGGCCAAGTAAGCTGTGGGCAGGCAAGCCCTTCGGTCACCTGTTGGCTACACAGACC AAACCCCTTGGCCAAGTAAGCTGTGGGCAGGCGAGCCCTTCGGTCACCTGTTGGCTACACAGACC T C ENO1 Ensembl:ENSG00000074800 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:8861039..8861414;chr1:8861075..8861402 26863196 MeRIP-seq:(Medium) rs770132290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221152,Human_RBP_ID_273210,Human_RBP_ID_364572,Human_RBP_ID_741594,Human_RBP_ID_980281,Human_RBP_ID_1436305,Human_RBP_ID_1755810,Human_RBP_ID_3324607,Human_RBP_ID_4099653,Human_RBP_ID_5538100,Human_RBP_ID_5876583,Human_RBP_ID_8320935,Human_RBP_ID_8752597,Human_RBP_ID_11137596,Human_RBP_ID_17220395,Human_RBP_ID_17337512,Human_RBP_ID_17455518,Human_RBP_ID_17646095,Human_RBP_ID_18186786,Human_RBP_ID_18582405,Human_RBP_ID_22426836,Human_RBP_ID_22488887,Human_RBP_ID_22786409,Human_RBP_ID_24454618,Human_RBP_ID_26870976,Human_RBP_ID_27153453,Human_RBP_ID_27187231 Human_Splice_Rec_14284,Human_Splice_Rec_14300,Human_Splice_Rec_14322,Human_Splice_Rec_14346 Human_miRNA_ID_2889097,Human_miRNA_ID_2889098 RMVar_hsa_circ_111730,RMVar_hsa_circ_125498,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_82100,RMVar_hsa_circ_96254,RMVar_hsa_circ_110519,RMVar_hsa_circ_87544,RMVar_hsa_circ_128759,RMVar_hsa_circ_75856,RMVar_hsa_circ_81903,RMVar_hsa_circ_128761,RMVar_hsa_circ_128762,RMVar_hsa_circ_128760,RMVar_hsa_circ_128757,RMVar_hsa_circ_128758,RMVar_hsa_circ_128756,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752 67315 RMVar_ID_67315 Human_SNP_ID_2451051 m1A Human chr1 - 8863338 8863338 8863338 CCATCTGGGTTGTTCCTTGGCTTCCAGGTGCAAGCTGGCCCAGGCCAATGGTTGGGGCGTCATGG CCATCTGGGTTGTTCCTTGGCTTCCAGGTGCAGGCTGGCCCAGGCCAATGGTTGGGGCGTCATGG T C ENO1 Ensembl:ENSG00000074800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:8863189..8863390 26863196 MeRIP-seq:(Medium) rs774084402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221155,Human_RBP_ID_741597,Human_RBP_ID_858211,Human_RBP_ID_18186793,Human_RBP_ID_22426840,Human_RBP_ID_22532034,Human_RBP_ID_24735329,Human_RBP_ID_26797600 Human_Splice_Rec_14280,Human_Splice_Rec_14296,Human_Splice_Rec_14318,Human_Splice_Rec_14342,Human_Splice_Rec_14364 Human_miRNA_ID_2660734,Human_miRNA_ID_2660735,Human_miRNA_ID_2679187,Human_miRNA_ID_2679188 RMVar_hsa_circ_35208,RMVar_hsa_circ_111730,RMVar_hsa_circ_125498,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_96254,RMVar_hsa_circ_87544,RMVar_hsa_circ_128759,RMVar_hsa_circ_75856,RMVar_hsa_circ_81903,RMVar_hsa_circ_128760,RMVar_hsa_circ_128757,RMVar_hsa_circ_128758,RMVar_hsa_circ_128756,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752,RMVar_hsa_circ_114730,RMVar_hsa_circ_292071,RMVar_hsa_circ_370462,RMVar_hsa_circ_330633,RMVar_hsa_circ_81090,RMVar_hsa_circ_128771,RMVar_hsa_circ_119744,RMVar_hsa_circ_128766,RMVar_hsa_circ_128768,RMVar_hsa_circ_128769,RMVar_hsa_circ_128767,RMVar_hsa_circ_128765,RMVar_hsa_circ_86209,RMVar_hsa_circ_128770,RMVar_hsa_circ_96569,RMVar_hsa_circ_115511,RMVar_hsa_circ_128772,RMVar_hsa_circ_128773 67316 RMVar_ID_67316 Human_SNP_ID_2451626 m1A Human chr1 - 8865366 8865364 8865366 TCTTCAGGTCTGGGAAGTATGACCTGGACTTCAAGTCTCCCGATGACCCCAGCAGGTACATCTCG TCTTCAGGTCTGGGAAGTATGACCTGGACTTC__GTCTCCCGATGACCCCAGCAGGTACATCTCG CTT C ENO1 Ensembl:ENSG00000074800 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8865259..8865442 26863196 MeRIP-seq:(Medium) rs1557580023 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17517,Human_RBP_ID_364612,Human_RBP_ID_980294,Human_RBP_ID_1436346,Human_RBP_ID_1755868,Human_RBP_ID_3324696,Human_RBP_ID_4068472,Human_RBP_ID_5156215,Human_RBP_ID_5876827,Human_RBP_ID_8320988,Human_RBP_ID_8752618,Human_RBP_ID_9269332,Human_RBP_ID_11138453,Human_RBP_ID_17220403,Human_RBP_ID_17455525,Human_RBP_ID_17668128,Human_RBP_ID_17759929,Human_RBP_ID_18468434,Human_RBP_ID_18582469,Human_RBP_ID_22426847,Human_RBP_ID_22488896,Human_RBP_ID_22531900,Human_RBP_ID_22748813,Human_RBP_ID_22786422,Human_RBP_ID_22875847,Human_RBP_ID_23122968,Human_RBP_ID_23418577,Human_RBP_ID_24454621,Human_RBP_ID_26871002,Human_RBP_ID_27187247,Human_RBP_ID_27599941 Human_Splice_Rec_14277,Human_Splice_Rec_14293,Human_Splice_Rec_14315,Human_Splice_Rec_14339,Human_Splice_Rec_14361 Human_miRNA_ID_2682567,Human_miRNA_ID_2682568,Human_miRNA_ID_3011168,Human_miRNA_ID_3011169 RMVar_hsa_circ_35208,RMVar_hsa_circ_125498,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_96254,RMVar_hsa_circ_75856,RMVar_hsa_circ_81903,RMVar_hsa_circ_128757,RMVar_hsa_circ_128758,RMVar_hsa_circ_128756,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752,RMVar_hsa_circ_114730,RMVar_hsa_circ_370462,RMVar_hsa_circ_81090,RMVar_hsa_circ_128771,RMVar_hsa_circ_119744,RMVar_hsa_circ_128768,RMVar_hsa_circ_128769,RMVar_hsa_circ_128767,RMVar_hsa_circ_96569,RMVar_hsa_circ_128772,RMVar_hsa_circ_124829,RMVar_hsa_circ_370083,RMVar_hsa_circ_128775,RMVar_hsa_circ_128776,RMVar_hsa_circ_128778,RMVar_hsa_circ_376211 67317 RMVar_ID_67317 Human_SNP_ID_2451672 m1A Human chr1 + 8865457 8865457 8865457 ATGACCACCTTATCAGTGTAGCCAGCTTTCCCAATAGCAGTCTTCAGCAGCTCCAGGCCTGGGAA ATGACCACCTTATCAGTGTAGCCAGCTTTCCCCATAGCAGTCTTCAGCAGCTCCAGGCCTGGGAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:8865245..8865527 26863196 MeRIP-seq:(Medium) rs1213802547 Functional Loss SNV dbSNP153 33..33 33 - - - 67318 RMVar_ID_67318 Human_SNP_ID_2453624 m1A Human chr1 + 8871842 8871842 8871842 ACCCAGAGAGGACAGGACTGGGCAAGGCCAGGAATGGGGCTGGAAGCAGGGAGGCCATGGGCTGT ACCCAGAGAGGACAGGACTGGGCAAGGCCAGGGATGGGGCTGGAAGCAGGGAGGCCATGGGCTGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8871838..8872027 26863196 MeRIP-seq:(Medium) rs777739455 Functional Loss SNV dbSNP153 33..33 33 - - - 67319 RMVar_ID_67319 Human_SNP_ID_2453628 m1A Human chr1 - 8871850 8871850 8871850 TAGAACCCACAGCCCATGGCCTCCCTGCTTCCAGCCCCATTCCTGGCCTTGCCCAGTCCTGTCCT TAGAACCCACAGCCCATGGCCTCCCTGCTTCCGGCCCCATTCCTGGCCTTGCCCAGTCCTGTCCT T C ENO1 Ensembl:ENSG00000074800 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:8871846..8871925 26863196 MeRIP-seq:(Medium) rs111412074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853673,Human_RBP_ID_5334709,Human_RBP_ID_19033817,Human_RBP_ID_22350659 RMVar_hsa_circ_35208,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128753,RMVar_hsa_circ_128754,RMVar_hsa_circ_128752,RMVar_hsa_circ_124829,RMVar_hsa_circ_128776,RMVar_hsa_circ_128782,RMVar_hsa_circ_128778,RMVar_hsa_circ_376211,RMVar_hsa_circ_76772,RMVar_hsa_circ_93328,RMVar_hsa_circ_81853,RMVar_hsa_circ_128783,RMVar_hsa_circ_128784,RMVar_hsa_circ_119235,RMVar_hsa_circ_103334,RMVar_hsa_circ_128788,RMVar_hsa_circ_128789 67320 RMVar_ID_67320 Human_SNP_ID_2454518 m1A Human chr1 - 8874902 8874902 8874902 GTGTGTTTCTTCTACAGAAGTTCACCATGTCTATTCTCAAGATCCATGCCAGGGAGATCTTTGAC GTGTGTTTCTTCTACAGAAGTTCACCATGTCTGTTCTCAAGATCCATGCCAGGGAGATCTTTGAC T C ENO1 Ensembl:ENSG00000074800 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8874851..8874979 26863196 MeRIP-seq:(Medium) rs759744149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858388,Human_RBP_ID_1156312,Human_RBP_ID_1350027,Human_RBP_ID_1436524,Human_RBP_ID_1756045,Human_RBP_ID_2171287,Human_RBP_ID_3324880,Human_RBP_ID_4075084,Human_RBP_ID_8321125,Human_RBP_ID_8752670,Human_RBP_ID_9318554,Human_RBP_ID_17220428,Human_RBP_ID_17760043,Human_RBP_ID_18186808,Human_RBP_ID_18582612,Human_RBP_ID_19451569,Human_RBP_ID_23150762,Human_RBP_ID_23418802,Human_RBP_ID_24454667,Human_RBP_ID_24736071,Human_RBP_ID_26797623 Human_Splice_Rec_14264,Human_Splice_Rec_14265,Human_Splice_Rec_14302,Human_Splice_Rec_14303,Human_Splice_Rec_14324,Human_Splice_Rec_14325,Human_Splice_Rec_14348,Human_Splice_Rec_14349,Human_Splice_Rec_14376,Human_Splice_Rec_14377,Human_Splice_Rec_14388,Human_Splice_Rec_14389,Human_Splice_Rec_14400,Human_Splice_Rec_14401,Human_Splice_Rec_14410,Human_Splice_Rec_14411,Human_Splice_Rec_14420,Human_Splice_Rec_14421,Human_Splice_Rec_14432,Human_Splice_Rec_14433,Human_Splice_Rec_14440,Human_Splice_Rec_14441,Human_Splice_Rec_14448,Human_Splice_Rec_14449,Human_Splice_Rec_14454,Human_Splice_Rec_14455 Human_miRNA_ID_2491892,Human_miRNA_ID_2864406,Human_miRNA_ID_2917584 RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128753,RMVar_hsa_circ_128752,RMVar_hsa_circ_124829,RMVar_hsa_circ_128776,RMVar_hsa_circ_128782,RMVar_hsa_circ_128778,RMVar_hsa_circ_376211,RMVar_hsa_circ_76772,RMVar_hsa_circ_93328,RMVar_hsa_circ_128783,RMVar_hsa_circ_119235,RMVar_hsa_circ_128009,RMVar_hsa_circ_128789,RMVar_hsa_circ_118160,RMVar_hsa_circ_112445,RMVar_hsa_circ_128791,RMVar_hsa_circ_128792,RMVar_hsa_circ_128794,RMVar_hsa_circ_81682,RMVar_hsa_circ_128793 67321 RMVar_ID_67321 Human_SNP_ID_2455647 m1A Human chr1 - 8878581 8878581 8878581 CTTCCTCTCCTAGGCGACGAGACCCAGTGGCTAGGTAATGATTGGGGAAGGGCTGAGCAACGGGC CTTCCTCTCCTAGGCGACGAGACCCAGTGGCTGGGTAATGATTGGGGAAGGGCTGAGCAACGGGC T C ENO1 Ensembl:ENSG00000074800 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:8878576..8878725 26863410 MeRIP-seq:(Medium) rs1223244155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_364726,Human_RBP_ID_980327,Human_RBP_ID_1436534,Human_RBP_ID_4073499,Human_RBP_ID_5312301,Human_RBP_ID_5414359,Human_RBP_ID_5434607,Human_RBP_ID_5458118,Human_RBP_ID_8321146,Human_RBP_ID_8976704,Human_RBP_ID_9318555,Human_RBP_ID_11140565,Human_RBP_ID_18430938,Human_RBP_ID_18582625,Human_RBP_ID_22147967,Human_RBP_ID_22488917,Human_RBP_ID_22786469,Human_RBP_ID_26591855,Human_RBP_ID_26797626,Human_RBP_ID_26871135,Human_RBP_ID_27187306,Human_RBP_ID_27401492 Human_Splice_Rec_14263,Human_Splice_Rec_14301,Human_Splice_Rec_14323,Human_Splice_Rec_14347,Human_Splice_Rec_14399,Human_Splice_Rec_14419,Human_Splice_Rec_14429,Human_Splice_Rec_14447,Human_Splice_Rec_14453 RMVar_hsa_circ_117677,RMVar_hsa_circ_128752,RMVar_hsa_circ_93328,RMVar_hsa_circ_128783,RMVar_hsa_circ_118160,RMVar_hsa_circ_112445,RMVar_hsa_circ_128792,RMVar_hsa_circ_128794 67322 RMVar_ID_67322 Human_SNP_ID_2455676 m1A Human chr1 + 8878631 8878631 8878631 GCCTAGGAGAGGAAGCGGAGGGTGCTGCAGACACCGAGGTGAACGTAAAGCCGGCGAGATCTCCG GCCTAGGAGAGGAAGCGGAGGGTGCTGCAGACCCCGAGGTGAACGTAAAGCCGGCGAGATCTCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:8878525..8878725;chr1:8878419..8878700;chr1:8878345..8878675;chr1:8878351..8878725;chr1:8874851..8878753;chr1:8878526..8878725 26863196 MeRIP-seq:(Medium) rs1462855429 Functional Loss SNV dbSNP153 33..33 33 - - - 67323 RMVar_ID_67323 Human_SNP_ID_2455938 m1A Human chr1 - 8879080 8879080 8879080 AGCAAGGTCGAGGGCCGGACGTGGGGCCCCAGAGCGACGCTGAGTGCGTGCGGGACTCGGAGTAC AGCAAGGTCGAGGGCCGGACGTGGGGCCCCAGGGCGACGCTGAGTGCGTGCGGGACTCGGAGTAC T C ENO1 Ensembl:ENSG00000074800 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8879030..8879215 26863196 MeRIP-seq:(Medium) rs1256337472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117677,RMVar_hsa_circ_128752,RMVar_hsa_circ_93328,RMVar_hsa_circ_128783,RMVar_hsa_circ_118160,RMVar_hsa_circ_112445,RMVar_hsa_circ_128792,RMVar_hsa_circ_128794 67324 RMVar_ID_67324 Human_SNP_ID_2516190 m1A Human chr1 - 9101398 9101398 9101398 AGTCTAGCTGGGTGGGTAGTGCTCAGACAGAAAGGCTGGATGGGAAGGAAGTCACATCCTAAAAG AGTCTAGCTGGGTGGGTAGTGCTCAGACAGAAGGGCTGGATGGGAAGGAAGTCACATCCTAAAAG T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:9101347..9101548 26863196 MeRIP-seq:(Medium) rs1275687873 Functional Loss SNV dbSNP153 33..33 33 - - - 67325 RMVar_ID_67325 Human_SNP_ID_2529360 m1A Human chr1 - 9149398 9149398 9149398 AAAAAATACAAAAATTAGCCAGGCATAGTGGCAGGACTGTAGTCCCAGCTACTCAGGAGGCTGAG AAAAAATACAAAAATTAGCCAGGCATAGTGGCGGGACTGTAGTCCCAGCTACTCAGGAGGCTGAG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs916722019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245760,Human_RBP_ID_11149851 67326 RMVar_ID_67326 Human_SNP_ID_2537591 m1A Human chr1 - 9182261 9182261 9182261 GGAGGAGATGCCGCTGTCCCGTCGGTCTGGGGACAGCCCAGCTCCCCGGATCCCGGGCTGGAGAG GGAGGAGATGCCGCTGTCCCGTCGGTCTGGGGGCAGCCCAGCTCCCCGGATCCCGGGCTGGAGAG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9182213..9182373 26863196 MeRIP-seq:(Medium) rs1235413372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5539314,Human_RBP_ID_17760833,Human_RBP_ID_18414845,Human_RBP_ID_18967103,Human_RBP_ID_23117620,Human_RBP_ID_24556159,Human_RBP_ID_24745078 Human_Splice_Rec_14666,Human_Splice_Rec_14668 RMVar_hsa_circ_33356 67327 RMVar_ID_67327 Human_SNP_ID_2551356 m1A Human chr1 - 9234846 9234846 9234846 CCCGCGGCGGCCGCAGGGGAAGGCGCGAGGCCAAGGCCAGCCCGGCCGCCACCCCGCCCCAGGCC CCCGCGGCGGCCGCAGGGGAAGGCGCGAGGCCCAGGCCAGCCCGGCCGCCACCCCGCCCCAGGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9234795..9235104 26863196 MeRIP-seq:(Medium) rs1423002572 Functional Loss SNV dbSNP153 33..33 33 - - - 67328 RMVar_ID_67328 Human_SNP_ID_2561307 m1A Human chr1 + 9269047 9269047 9269047 TGGGGCTCCCTTAGAACTTACTCCACTGATTTAAAAAAAAAAAACTGCCTGGCAGCATCTCAGTG TGGGGCTCCCTTAGAACTTACTCCACTGATTTTAAAAAAAAAAACTGCCTGGCAGCATCTCAGTG A T H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11121355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27401788 Human_miRNA_ID_2278672,Human_miRNA_ID_2458734,Human_miRNA_ID_2638982 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 67329 RMVar_ID_67329 Human_SNP_ID_2567373 m1A Human chr1 - 9292944 9292944 9292944 CCCGCGGCCCCGGCCCCGGCGCCGGCGCCTGGAGCCTGGTTCCTGCTGCGAGCGCGCAGGCTGCC CCCGCGGCCCCGGCCCCGGCGCCGGCGCCTGGGGCCTGGTTCCTGCTGCGAGCGCGCAGGCTGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:9292895..9293260 26863196 MeRIP-seq:(Medium) rs984724522 Functional Loss SNV dbSNP153 33..33 33 - - - 67330 RMVar_ID_67330 Human_SNP_ID_2567806 m1A Human chr1 + 9294128 9294128 9294128 GTGTCTTTGTGTGTGTCTGTGTGTGAGTGTGTATGTGTCTTTGGGTGTGTGTCTCTGCAAGTTTG GTGTCTTTGTGTGTGTCTGTGTGTGAGTGTGTCTGTGTCTTTGGGTGTGTGTCTCTGCAAGTTTG A C SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:9294078..9294305 26863196 MeRIP-seq:(Medium) rs1001368867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67331 RMVar_ID_67331 Human_SNP_ID_2567807 m1A Human chr1 + 9294128 9294128 9294128 GTGTCTTTGTGTGTGTCTGTGTGTGAGTGTGTATGTGTCTTTGGGTGTGTGTCTCTGCAAGTTTG GTGTCTTTGTGTGTGTCTGTGTGTGAGTGTGTGTGTGTCTTTGGGTGTGTGTCTCTGCAAGTTTG A G SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:9294078..9294305 26863196 MeRIP-seq:(Medium) rs1001368867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67332 RMVar_ID_67332 Human_SNP_ID_2577380 m1A Human chr1 + 9329298 9329298 9329298 AAAGGTGAGATCCCGGATGGGTGGATGGGTGGACAGGTGGACAGGCGGATGGGTGGACGTGTGTG AAAGGTGAGATCCCGGATGGGTGGATGGGTGGGCAGGTGGACAGGCGGATGGGTGGACGTGTGTG A G SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:9329200..9329388 26863196 MeRIP-seq:(Medium) rs1403410791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67333 RMVar_ID_67333 Human_SNP_ID_2577404 m1A Human chr1 + 9329399 9329395 9329400 AGGGCAGTGATGGAGAGGTCAGGGGAGGTGACACCCGGTGGTGGGTAGGTCAGGTGAGAGGATCC AGGGCAGTGATGGAGAGGTCAGGGGAGGT_____CCGGTGGTGGGTAGGTCAGGTGAGAGGATCC TGACAC T SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:9329176..9329440 26863196 MeRIP-seq:(Medium) rs1331649188 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67334 RMVar_ID_67334 Human_SNP_ID_2578250 m1A Human chr1 + 9332289 9332286 9332289 ACTTGGAGACTCTTGCAGTGGCCTTGCAAGTGATGACTTAAACAGTGAGAGTGAAGGTGGGATTC ACTTGGAGACTCTTGCAGTGGCCTTGCAAG___TGACTTAAACAGTGAGAGTGAAGGTGGGATTC GTGA G SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9332286..9332623 26863196 MeRIP-seq:(Medium) rs1291218866 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67335 RMVar_ID_67335 Human_SNP_ID_2578261 m1A Human chr1 + 9332329 9332329 9332329 AACAGTGAGAGTGAAGGTGGGATTCAGCAACTATGGGGGCAGCAATTTACAATGTTTGGCGCTAA AACAGTGAGAGTGAAGGTGGGATTCAGCAACTGTGGGGGCAGCAATTTACAATGTTTGGCGCTAA A G SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:9332326..9332530 26863196 MeRIP-seq:(Medium) rs544885454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67336 RMVar_ID_67336 Human_SNP_ID_2582752 m1A Human chr1 + 9349431 9349430 9349432 GGCCAGGAGTGGGGGTAGGTGAGTGTGGGGTCAGGGGGCTGTCCCAGCTGAGCTCAACCAGAGAG GGCCAGGAGTGGGGGTAGGTGAGTGTGGGGTC__GGGGCTGTCCCAGCTGAGCTCAACCAGAGAG CAG C SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9349429..9349515 26863196 MeRIP-seq:(Medium) rs958279306 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 67337 RMVar_ID_67337 Human_SNP_ID_2584524 m1A Human chr1 + 9355793 9355793 9355793 CAGCTTGCAGAGGTCTCCTGGCAGCCCTCATTAGGAATTCTGTCTGGCCCCGATCAGAATACTGG CAGCTTGCAGAGGTCTCCTGGCAGCCCTCATTGGGAATTCTGTCTGGCCCCGATCAGAATACTGG A G SPSB1 Ensembl:ENSG00000171621 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9355726..9356004 26863196 MeRIP-seq:(Medium) rs1339447673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075098 Human_Splice_Rec_14714,Human_Splice_Rec_14718,Human_Splice_Rec_14720 Human_miRNA_ID_2660738,Human_miRNA_ID_2679191 RMVar_hsa_circ_79802,RMVar_hsa_circ_128803,RMVar_hsa_circ_116564,RMVar_hsa_circ_293469,RMVar_hsa_circ_128804,RMVar_hsa_circ_128805 67338 RMVar_ID_67338 Human_SNP_ID_2585023 m1A Human chr1 + 9357220 9357220 9357220 GATGGATGGATGGGTGGATGGATCAGTGAATGAATGGATGGATGGATGGATGGATAAATGAACAG GATGGATGGATGGGTGGATGGATCAGTGAATGGATGGATGGATGGATGGATGGATAAATGAACAG A G SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:9356880..9357369 26863196 MeRIP-seq:(Medium) rs75850835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79802,RMVar_hsa_circ_128805 67339 RMVar_ID_67339 Human_SNP_ID_2587925 m1A Human chr1 + 9367689 9367689 9367689 CACCTTGGACCGGCATCCGTAGCCATGGACAGAGGTCCCTGGTCTTCCCTCATCCTCCGTGGCTG CACCTTGGACCGGCATCCGTAGCCATGGACAGGGGTCCCTGGTCTTCCCTCATCCTCCGTGGCTG A G SPSB1 Ensembl:ENSG00000171621 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9367639..9367721 26863196 MeRIP-seq:(Medium) rs566779186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98634,Human_RBP_ID_27401924 RMVar_hsa_circ_79802,RMVar_hsa_circ_128805 67340 RMVar_ID_67340 Human_SNP_ID_2633533 m1A Human chr1 + 9539514 9539514 9539514 GCGCCGCAGAGGCCGGTGAGGCGCCGGCGGCCACGCCGCGGAAGGCGCGGGCCGAGCAGAGCCGG GCGCCGCAGAGGCCGGTGAGGCGCCGGCGGCCCCGCCGCGGAAGGCGCGGGCCGAGCAGAGCCGG A C SLC25A33 Ensembl:ENSG00000171612 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9539509..9539611 26863196 MeRIP-seq:(Medium) rs1283934298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072498,Human_RBP_ID_18414847 67341 RMVar_ID_67341 Human_SNP_ID_2643712 m1A Human chr1 - 9577551 9577551 9577551 TTCTCCAGCGCAGATGCACGTACTACACGCCAACTACACTCCCTGTCTTACGGCTCCCCAGAACT TTCTCCAGCGCAGATGCACGTACTACACGCCAGCTACACTCCCTGTCTTACGGCTCCCCAGAACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:9577503..9577632 26863196 MeRIP-seq:(Medium) rs913406738 Functional Loss SNV dbSNP153 33..33 33 - - - 67342 RMVar_ID_67342 Human_SNP_ID_2646843 m1A Human chr1 + 9588868 9588844 9588868 GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTG________________________CCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTGCCCGCCTA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:9588767..9588871 26863410 MeRIP-seq:(Medium) rs1388324076 Functional Loss DEL dbSNP153 10..33 33 - - - 67343 RMVar_ID_67343 Human_SNP_ID_2646847 m1A Human chr1 - 9588875 9588852 9588876 AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGGTAGGCGGGTAGGCGGGCAGGCGGGCAGGCGGGCA AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGG________________________CAGGCGGGCA GCCCGCCTGCCCGCCTACCCGCCTA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9588796..9589006 26863196 MeRIP-seq:(Medium) rs980748487 Functional Loss DEL dbSNP153 32..55 33 - - - 67344 RMVar_ID_67344 Human_SNP_ID_2646848 m1A Human chr1 + 9588868 9588852 9588868 GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTG________________CCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:9588767..9588871 26863410 MeRIP-seq:(Medium) rs1159481621 Functional Loss DEL dbSNP153 18..33 33 - - - 67345 RMVar_ID_67345 Human_SNP_ID_2646855 m1A Human chr1 - 9588875 9588860 9588876 AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGGTAGGCGGGTAGGCGGGCAGGCGGGCAGGCGGGCA AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGG________________CAGGCGGGCAGGCGGGCA GCCCGCCTACCCGCCTA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9588796..9589006 26863196 MeRIP-seq:(Medium) rs1230900177 Functional Loss DEL dbSNP153 32..47 33 - - - 67346 RMVar_ID_67346 Human_SNP_ID_2646856 m1A Human chr1 - 9588875 9588860 9588876 AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGGTAGGCGGGTAGGCGGGCAGGCGGGCAGGCGGGCA AGGCCGGCAGGGGGGTAGGCGGGTAGGCGGG________TAGGCGGGCAGGCGGGCAGGCGGGCA GCCCGCCTACCCGCCTA GCCCGCCTA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9588796..9589006 26863196 MeRIP-seq:(Medium) rs1230900177 Functional Loss DEL dbSNP153 32..39 33 - - - 67347 RMVar_ID_67347 Human_SNP_ID_2646861 m1A Human chr1 + 9588868 9588868 9588868 GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTCCCCGCCTACCCGCCTACCCGCCTACCCCCCTG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:9588767..9588871 26863410 MeRIP-seq:(Medium) rs867507444 Functional Loss SNV dbSNP153 33..33 33 - - - 67348 RMVar_ID_67348 Human_SNP_ID_2646862 m1A Human chr1 + 9588868 9588868 9588868 GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCCCCTG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:9588767..9588871 26863410 MeRIP-seq:(Medium) rs867507444 Functional Loss SNV dbSNP153 33..33 33 - - - 67349 RMVar_ID_67349 Human_SNP_ID_2674679 m1A Human chr1 + 9693764 9693764 9693764 TATGAACAAAACCTTTGCAGGACAGGAAACCGATAGGCGAGAGGGAAGCTGAGTGGAGAATGTCC TATGAACAAAACCTTTGCAGGACAGGAAACCGTTAGGCGAGAGGGAAGCTGAGTGGAGAATGTCC A T PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9693760..9693889 26863196 MeRIP-seq:(Medium) rs1166016374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27102 67350 RMVar_ID_67350 Human_SNP_ID_2684697 m1A Human chr1 - 9730597 9730597 9730597 AGGATGACATCACCAGCGCCGAGTCGGAGAGCAGCGAGGAGGAGGAGGGGGAGCAGGGCGACCCC AGGATGACATCACCAGCGCCGAGTCGGAGAGCGGCGAGGAGGAGGAGGGGGAGCAGGGCGACCCC T C CLSTN1 Ensembl:ENSG00000171603 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:9730476..9730650 26863196 MeRIP-seq:(Medium) rs1329802827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222888,Human_RBP_ID_5158032,Human_RBP_ID_5538161,Human_RBP_ID_5889245,Human_RBP_ID_8228560,Human_RBP_ID_8978013,Human_RBP_ID_9355452,Human_RBP_ID_18964613,Human_RBP_ID_22428040,Human_RBP_ID_22750656,Human_RBP_ID_26310157,Human_RBP_ID_27797313 RMVar_hsa_circ_85258,RMVar_hsa_circ_121065,RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_128821,RMVar_hsa_circ_128822 67351 RMVar_ID_67351 Human_SNP_ID_2685906 m1A Human chr1 - 9734136 9734136 9734136 TATTTCTGGTTGGGCCTCTTTTGCAGTTCAAGAATCACTGGTGTCCGAGGAGATCGTGCACGACC TATTTCTGGTTGGGCCTCTTTTGCAGTTCAAGGATCACTGGTGTCCGAGGAGATCGTGCACGACC T C CLSTN1 Ensembl:ENSG00000171603 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:9734101..9734150 26863196 MeRIP-seq:(Medium) rs1290507745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22952,Human_RBP_ID_802216 Human_Splice_Rec_15066,Human_Splice_Rec_15102,Human_Splice_Rec_15134,Human_Splice_Rec_15168 RMVar_hsa_circ_85258,RMVar_hsa_circ_121065,RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_128821,RMVar_hsa_circ_128822,RMVar_hsa_circ_15648,RMVar_hsa_circ_91160,RMVar_hsa_circ_15408,RMVar_hsa_circ_128824 67352 RMVar_ID_67352 Human_SNP_ID_2695513 m1A Human chr1 - 9768191 9768191 9768191 GCCGTCCAGGACAACCCCGCCCCCATGGTGCCACCCAGCACAGAACAGGACCCTATGAGACTGAG GCCGTCCAGGACAACCCCGCCCCCATGGTGCCGCCCAGCACAGAACAGGACCCTATGAGACTGAG T C CLSTN1 Ensembl:ENSG00000171603 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9768186..9768397 26863196 MeRIP-seq:(Medium) rs9430238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125576,Human_RBP_ID_11174329,Human_RBP_ID_18929226 RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_77987,RMVar_hsa_circ_348056,RMVar_hsa_circ_128830,RMVar_hsa_circ_299941,RMVar_hsa_circ_128832,RMVar_hsa_circ_128833,RMVar_hsa_circ_325603 67353 RMVar_ID_67353 Human_SNP_ID_2697190 m1A Human chr1 - 9773392 9773392 9773392 GTCTATTTTTTTCTCTTGTTTTAAACACAGTTAACAAGCACAAGCCCTGGCTGGAGCCCACCTAC GTCTATTTTTTTCTCTTGTTTTAAACACAGTTGACAAGCACAAGCCCTGGCTGGAGCCCACCTAC T C CLSTN1 Ensembl:ENSG00000171603 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr1:9773301..9773491;chr1:9773375..9773460 26863196,26863410 MeRIP-seq:(Medium) rs750754639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075106,Human_RBP_ID_22428050,Human_RBP_ID_26799831 Human_Splice_Rec_15040,Human_Splice_Rec_15076,Human_Splice_Rec_15144 Human_miRNA_ID_2235718,Human_miRNA_ID_2971986 RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_77987,RMVar_hsa_circ_348056,RMVar_hsa_circ_128830,RMVar_hsa_circ_299941,RMVar_hsa_circ_128832,RMVar_hsa_circ_128833,RMVar_hsa_circ_128837,RMVar_hsa_circ_325603,RMVar_hsa_circ_128838,RMVar_hsa_circ_375937 67354 RMVar_ID_67354 Human_SNP_ID_2697192 m1A Human chr1 + 9773394 9773394 9773394 AGGTGGGCTCCAGCCAGGGCTTGTGCTTGTTAACTGTGTTTAAAACAAGAGAAAAAAATAGACAA AGGTGGGCTCCAGCCAGGGCTTGTGCTTGTTAGCTGTGTTTAAAACAAGAGAAAAAAATAGACAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:9773376..9773400 26863196 MeRIP-seq:(Medium) rs202203353 Functional Loss SNV dbSNP153 33..33 33 - - - 67355 RMVar_ID_67355 Human_SNP_ID_2710982 m1A Human chr1 + 9823413 9823411 9823413 TGGCTTCCCCGGGACGCCTGCAGCGCGCGCCCACAGTCTCCTGCGCCCTGGCCCCGGCTCCGCGA TGGCTTCCCCGGGACGCCTGCAGCGCGCGCC__CAGTCTCCTGCGCCCTGGCCCCGGCTCCGCGA CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:9823408..9823624 26863196 MeRIP-seq:(Medium) rs1218366337 Functional Loss DEL dbSNP153 32..33 33 - - - 67356 RMVar_ID_67356 Human_SNP_ID_2711009 m1A Human chr1 - 9823484 9823484 9823484 CGGGATGCGGGGAGTCGGGTCCGAGCGCAGGGAGCCGGGTCAGGGCGTGGGGTTCGGGTTGGGGG CGGGATGCGGGGAGTCGGGTCCGAGCGCAGGGGGCCGGGTCAGGGCGTGGGGTTCGGGTTGGGGG T C CLSTN1 Ensembl:ENSG00000171603 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:9823479..9823618 26863196 MeRIP-seq:(Medium) rs529013111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_77987,RMVar_hsa_circ_128832 67357 RMVar_ID_67357 Human_SNP_ID_2711043 m1A Human chr1 + 9823607 9823607 9823607 ACCCGAATCCTGCACCCGGACCCGAATCCCGCACCGACCCAGCGGCCCGGCCCAGCCCCGGGGCT ACCCGAATCCTGCACCCGGACCCGAATCCCGCGCCGACCCAGCGGCCCGGCCCAGCCCCGGGGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr1:9823601..9823950;chr1:9823604..9823705 26863196,32194978 MeRIP-seq:(Medium) rs975041533 Functional Loss SNV dbSNP153 33..33 33 - - - 67358 RMVar_ID_67358 Human_SNP_ID_2711099 m1A Human chr1 + 9823807 9823798 9823807 CCGAGCGGAGCTCTCGGAGCTCTCGGGGCTCTAGGGGCCTGGGGCTAGCTGCTCCGCGGCGCGGG CCGAGCGGAGCTCTCGGAGCTCTC_________GGGGCCTGGGGCTAGCTGCTCCGCGGCGCGGG CGGGGCTCTA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:9823676..9823975 26863196 MeRIP-seq:(Medium) rs1258855964 Functional Loss DEL dbSNP153 25..33 33 - - - 67359 RMVar_ID_67359 Human_SNP_ID_2711143 m1A Human chr1 + 9823905 9823905 9823905 CCGCCGCCGTGACGCTGGGCCGCGCGCTCAGGACGCGGCGCCCTCCCCGCCTCAGAGCAGCGTCT CCGCCGCCGTGACGCTGGGCCGCGCGCTCAGGGCGCGGCGCCCTCCCCGCCTCAGAGCAGCGTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:9823602..9823955;chr1:9823751..9823950;chr1:9823726..9823975;chr1:9823752..9823925 26863196 MeRIP-seq:(Medium) rs1279289298 Functional Loss SNV dbSNP153 33..33 33 - - - 67360 RMVar_ID_67360 Human_SNP_ID_2717417 m1A Human chr1 + 9848473 9848473 9848473 GGGGCAGAGACCACACACTCAACCAGGTATCCACCAGGTGTGGGCCCTTTATAGGAGCTACAAAG GGGGCAGAGACCACACACTCAACCAGGTATCCGCCAGGTGTGGGCCCTTTATAGGAGCTACAAAG A G AL357140.1 Ensembl:ENSG00000223989 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:9848424..9849472 32194978 MeRIP-seq:(Medium) rs1357933064 Functional Loss SNV dbSNP153 33..33 33 - - - 67361 RMVar_ID_67361 Human_SNP_ID_2717999 m1A Human chr1 + 9850667 9850667 9850667 GGCTGCTGCCACTCAGCCGGCCCAGGAGCCACACAGATCTCTTGGCCCTCAACAGCATCCAGGGT GGCTGCTGCCACTCAGCCGGCCCAGGAGCCACGCAGATCTCTTGGCCCTCAACAGCATCCAGGGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:9850617..9871277 32194978 MeRIP-seq:(Medium) rs1003550049 Functional Loss SNV dbSNP153 33..33 33 - - - 67362 RMVar_ID_67362 Human_SNP_ID_2737392 m1A Human chr1 - 9928751 9928751 9928751 CTGCCTCAGCTTCCCAAGTAGCTGGGATTACTAGTGTGTACCACCACGCCCAGCTAATTTTTGTA CTGCCTCAGCTTCCCAAGTAGCTGGGATTACTGGTGTGTACCACCACGCCCAGCTAATTTTTGTA T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs149715018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128844 67363 RMVar_ID_67363 Human_SNP_ID_2741290 m1A Human chr1 + 9943266 9943265 9943266 TCCTTCCGGGCCTACCTGACAAAAACTGGGACAACCTCCTTAGGCCCCCGGGATTCCCCCTGTGC TCCTTCCGGGCCTACCTGACAAAAACTGGGAC_ACCTCCTTAGGCCCCCGGGATTCCCCCTGTGC CA C AL357140.2 Ensembl:ENSG00000228150 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9943238..9943309 26863196 MeRIP-seq:(Medium) rs1316393216 Functional Loss DEL dbSNP153 33..33 33 - - - 67364 RMVar_ID_67364 Human_SNP_ID_2741394 m1A Human chr1 - 9943517 9943517 9943517 CCAGTTTCTCAGGGGCTCCTTGCGGGGAGCTTACCGCGCCCTCACTGTCCGCCGGCCCGAGTGCT CCAGTTTCTCAGGGGCTCCTTGCGGGGAGCTTGCCGCGCCCTCACTGTCCGCCGGCCCGAGTGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:9943499..9943596;chr1:9943499..9943599 26863196 MeRIP-seq:(Medium) rs1354323616 Functional Loss SNV dbSNP153 33..33 33 - - - 67365 RMVar_ID_67365 Human_SNP_ID_2741395 m1A Human chr1 + 9943519 9943519 9943519 CACTCGGGCCGGCGGACAGTGAGGGCGCGGTAAGCTCCCCGCAAGGAGCCCCTGAGAAACTGGTC CACTCGGGCCGGCGGACAGTGAGGGCGCGGTAGGCTCCCCGCAAGGAGCCCCTGAGAAACTGGTC A G AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:9943498..9943593 26863196 MeRIP-seq:(Medium) rs957312118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18414850 67366 RMVar_ID_67366 Human_SNP_ID_2757456 m1A Human chr1 + 10007619 10007619 10007619 CGTAAAATAGCCAAGTTGCTGAAGCCACAGAAAGTGATTGAGCAGAATGGGGATTCTTTTACCAT CGTAAAATAGCCAAGTTGCTGAAGCCACAGAAGGTGATTGAGCAGAATGGGGATTCTTTTACCAT A G RBP7 Ensembl:ENSG00000162444 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:10004300..10007707 32194978 MeRIP-seq:(Medium) rs755529698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_15314,Human_Splice_Rec_15320 RMVar_hsa_circ_128857,RMVar_hsa_circ_352394 67367 RMVar_ID_67367 Human_SNP_ID_2757641 m1A Human chr1 - 10008273 10008273 10008273 CATCTCATTAAGAACAAAATGTGGTGGATACCAGGTGGAGTTTGTCTCCTTCGATCCAATGGGTC CATCTCATTAAGAACAAAATGTGGTGGATACCGGGTGGAGTTTGTCTCCTTCGATCCAATGGGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:10008225..10015972 32194978 MeRIP-seq:(Medium) rs779775745 Functional Loss SNV dbSNP153 33..33 33 - - - 67368 RMVar_ID_67368 Human_SNP_ID_2764090 m1A Human chr1 - 10033215 10033215 10033215 CTTTGCTCCTGGCGGGAACTGGTCGACTGCAGAGTGGATACCCCGAGGTAAGGCGACCCCACAGC CTTTGCTCCTGGCGGGAACTGGTCGACTGCAGGGTGGATACCCCGAGGTAAGGCGACCCCACAGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:10033030..10033225 26863196 MeRIP-seq:(Medium) rs1296850236 Functional Loss SNV dbSNP153 33..33 33 - - - 67369 RMVar_ID_67369 Human_SNP_ID_2765902 m1A Human chr1 - 10039810 10039810 10039810 GTCTGCAGCCACCTTCTCCCAAACTACCCTTTACTCCCTTGCCACCCATCTTTCTAATCTCTTAA GTCTGCAGCCACCTTCTCCCAAACTACCCTTTTCTCCCTTGCCACCCATCTTTCTAATCTCTTAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:10039803..10040046 26863196 MeRIP-seq:(Medium) rs1209592339 Functional Loss SNV dbSNP153 33..33 33 - - - 67370 RMVar_ID_67370 Human_SNP_ID_2767512 m1A Human chr1 + 10045740 10045740 10045740 AGTCCCAGGGAGAGATGATGTGGGGGCCACCAACTGGGGTTAGTGGTTGAGAGGGGGAGAAAGGG AGTCCCAGGGAGAGATGATGTGGGGGCCACCAGCTGGGGTTAGTGGTTGAGAGGGGGAGAAAGGG A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10045736..10045853 26863196 MeRIP-seq:(Medium) rs910938526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859 67371 RMVar_ID_67371 Human_SNP_ID_2767513 m1A Human chr1 + 10045740 10045740 10045740 AGTCCCAGGGAGAGATGATGTGGGGGCCACCAACTGGGGTTAGTGGTTGAGAGGGGGAGAAAGGG AGTCCCAGGGAGAGATGATGTGGGGGCCACCATCTGGGGTTAGTGGTTGAGAGGGGGAGAAAGGG A T UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10045736..10045853 26863196 MeRIP-seq:(Medium) rs910938526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859 67372 RMVar_ID_67372 Human_SNP_ID_2784697 m1A Human chr1 + 10116156 10116156 10116156 CATTCCTGATGTTCCCATACTTTTTTTCTTTTATTTTAGGACAGCGTCTCTCTTTGTCGCCCAGG CATTCCTGATGTTCCCATACTTTTTTTCTTTTTTTTTAGGACAGCGTCTCTCTTTGTCGCCCAGG A T UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:10116140..10116227 26863410 MeRIP-seq:(Medium) rs1206968250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5662835 RMVar_hsa_circ_90073,RMVar_hsa_circ_4601,RMVar_hsa_circ_128859,RMVar_hsa_circ_12294,RMVar_hsa_circ_301021,RMVar_hsa_circ_356658,RMVar_hsa_circ_324696,RMVar_hsa_circ_18914,RMVar_hsa_circ_342817,RMVar_hsa_circ_128861,RMVar_hsa_circ_128862,RMVar_hsa_circ_128864,RMVar_hsa_circ_330109,RMVar_hsa_circ_330657,RMVar_hsa_circ_34341,RMVar_hsa_circ_128867,RMVar_hsa_circ_40282,RMVar_hsa_circ_340497,RMVar_hsa_circ_373995,RMVar_hsa_circ_128865,RMVar_hsa_circ_345359,RMVar_hsa_circ_27405 67373 RMVar_ID_67373 Human_SNP_ID_2809982 m1A Human chr1 - 10210637 10210637 10210637 GGGAGGCCAGGGCGCGGCGACGGCCGGCGGTGACGGCTGCGGAGGACGGGGAGCTGCTCCGACGC GGGAGGCCAGGGCGCGGCGACGGCCGGCGGTGTCGGCTGCGGAGGACGGGGAGCTGCTCCGACGC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr1:10210551..10210750;chr1:10210586..10210728 26863410,26863196 MeRIP-seq:(Medium) rs1008702861 Functional Loss SNV dbSNP153 33..33 33 - - - 67374 RMVar_ID_67374 Human_SNP_ID_2833656 m1A Human chr1 + 10303553 10303553 10303553 CCAATGAGCGGGACTCCTGGAGGGCAGTGGCCAGGGACGTCTGGGATACCGTCGGTGTTGGGGAT CCAATGAGCGGGACTCCTGGAGGGCAGTGGCCGGGGACGTCTGGGATACCGTCGGTGTTGGGGAT A G KIF1B Ensembl:ENSG00000054523 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:10303505..10303655 26863196 MeRIP-seq:(Medium) rs781157722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26313284 RMVar_hsa_circ_52418,RMVar_hsa_circ_4505,RMVar_hsa_circ_128898,RMVar_hsa_circ_268423,RMVar_hsa_circ_66971,RMVar_hsa_circ_340188,RMVar_hsa_circ_128927,RMVar_hsa_circ_76819,RMVar_hsa_circ_87364,RMVar_hsa_circ_1562,RMVar_hsa_circ_128934,RMVar_hsa_circ_265362,RMVar_hsa_circ_268567,RMVar_hsa_circ_22365,RMVar_hsa_circ_10984,RMVar_hsa_circ_869,RMVar_hsa_circ_128935,RMVar_hsa_circ_128937,RMVar_hsa_circ_128936,RMVar_hsa_circ_118172,RMVar_hsa_circ_339750,RMVar_hsa_circ_128942,RMVar_hsa_circ_346490,RMVar_hsa_circ_338124,RMVar_hsa_circ_8455,RMVar_hsa_circ_58805,RMVar_hsa_circ_128944,RMVar_hsa_circ_128943,RMVar_hsa_circ_325288,RMVar_hsa_circ_334798,RMVar_hsa_circ_128948,RMVar_hsa_circ_22360,RMVar_hsa_circ_290613 67375 RMVar_ID_67375 Human_SNP_ID_2857477 m1A Human chr1 - 10399095 10399095 10399095 ACTGGGCCATGGCGGCGGACAGAGCAGAACCGAAGAGCGGCGACGCGCGGAGGACGAGTGAGGGA ACTGGGCCATGGCGGCGGACAGAGCAGAACCGCAGAGCGGCGACGCGCGGAGGACGAGTGAGGGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:10399076..10399246;chr1:10399076..10399150 26863196 MeRIP-seq:(Medium) rs770405684 Functional Loss SNV dbSNP153 33..33 33 - - - 67376 RMVar_ID_67376 Human_SNP_ID_2857693 m1A Human chr1 - 10399637 10399637 10399637 TCTGGCCCATGACGGCCAATCCGATCAGCGCGATGTCAGCTCTAGAGAGGCAGAAACAGAACAAA TCTGGCCCATGACGGCCAATCCGATCAGCGCGCTGTCAGCTCTAGAGAGGCAGAAACAGAACAAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10399626..10399725 26863196 MeRIP-seq:(Medium) rs749202787 Functional Loss SNV dbSNP153 33..33 33 - - - 67377 RMVar_ID_67377 Human_SNP_ID_2857920 m1A Human chr1 - 10400348 10400348 10400348 AAGTCCTGAGTAGGAGATCCAGGACACACAAGACTTTCAGACTGTGGCCAAAGTAACAATGACCT AAGTCCTGAGTAGGAGATCCAGGACACACAAGGCTTTCAGACTGTGGCCAAAGTAACAATGACCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10400345..10400475 26863196 MeRIP-seq:(Medium) rs1242893577 Functional Loss SNV dbSNP153 33..33 33 - - - 67378 RMVar_ID_67378 Human_SNP_ID_2859049 m1A Human chr1 + 10404274 10404274 10404274 GGCCCATCGCTCATGCCAGGAGGGAACAAAGAAGCGTGGTGAGTGCCATCAGCACTGTGCCCATC GGCCCATCGCTCATGCCAGGAGGGAACAAAGATGCGTGGTGAGTGCCATCAGCACTGTGCCCATC A T PGD Ensembl:ENSG00000142657 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:10404226..10408150 32194978 MeRIP-seq:(Medium) rs1018174217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741346,Human_RBP_ID_22428055,Human_RBP_ID_22469681,Human_RBP_ID_24358677 Human_Splice_Rec_16141,Human_Splice_Rec_16153,Human_Splice_Rec_16191,Human_Splice_Rec_16197 RMVar_hsa_circ_76698,RMVar_hsa_circ_87015,RMVar_hsa_circ_36426,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128996,RMVar_hsa_circ_128997,RMVar_hsa_circ_105327,RMVar_hsa_circ_290158,RMVar_hsa_circ_377628,RMVar_hsa_circ_128998,RMVar_hsa_circ_308966,RMVar_hsa_circ_273143,RMVar_hsa_circ_61009,RMVar_hsa_circ_39853,RMVar_hsa_circ_128999,RMVar_hsa_circ_129000,RMVar_hsa_circ_129001,RMVar_hsa_circ_278746,RMVar_hsa_circ_299511,RMVar_hsa_circ_361699,RMVar_hsa_circ_90592,RMVar_hsa_circ_129002,RMVar_hsa_circ_129003,RMVar_hsa_circ_129004 67379 RMVar_ID_67379 Human_SNP_ID_2860993 m1A Human chr1 + 10411468 10411468 10411468 GGCCACTTCGTGAAGATGGTGCACAACGGGATAGAGTATGGGGACATGCAGCTGATCTGTGAGGC GGCCACTTCGTGAAGATGGTGCACAACGGGATCGAGTATGGGGACATGCAGCTGATCTGTGAGGC A C PGD Ensembl:ENSG00000142657 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:10411352..10411500 26863196 MeRIP-seq:(Medium) rs899912122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5663802,Human_RBP_ID_10499545,Human_RBP_ID_17719784,Human_RBP_ID_22636128,Human_RBP_ID_22750666,Human_RBP_ID_23319712 Human_Splice_Rec_16155,Human_Splice_Rec_16178,Human_Splice_Rec_16179,Human_Splice_Rec_16199 RMVar_hsa_circ_76698,RMVar_hsa_circ_87015,RMVar_hsa_circ_36426,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128996,RMVar_hsa_circ_128997,RMVar_hsa_circ_105327,RMVar_hsa_circ_290158,RMVar_hsa_circ_377628,RMVar_hsa_circ_128998,RMVar_hsa_circ_61009,RMVar_hsa_circ_66062,RMVar_hsa_circ_39853,RMVar_hsa_circ_129000,RMVar_hsa_circ_129001,RMVar_hsa_circ_299511,RMVar_hsa_circ_361699,RMVar_hsa_circ_90592,RMVar_hsa_circ_129003,RMVar_hsa_circ_129004,RMVar_hsa_circ_268031,RMVar_hsa_circ_351502,RMVar_hsa_circ_88420,RMVar_hsa_circ_129006,RMVar_hsa_circ_122759,RMVar_hsa_circ_129005,RMVar_hsa_circ_37014,RMVar_hsa_circ_340027,RMVar_hsa_circ_377350,RMVar_hsa_circ_292897,RMVar_hsa_circ_129007 67380 RMVar_ID_67380 Human_SNP_ID_2861028 m1A Human chr1 - 10411524 10411524 10411524 TCACCTGGGCCATCTCGTCCTGCGCCATGCCCAGCACGTCTTTCATCAGGTGGTATGCCTCACAG TCACCTGGGCCATCTCGTCCTGCGCCATGCCCCGCACGTCTTTCATCAGGTGGTATGCCTCACAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10411501..10411525 26863196 MeRIP-seq:(Medium) rs1192044285 Functional Loss SNV dbSNP153 33..33 33 - - - 67381 RMVar_ID_67381 Human_SNP_ID_2863049 m1A Human chr1 + 10418876 10418876 10418876 AAAGGATGCATTTGATCGAAACCCGGAACTTCAGAACCTCCTACTGGACGACTTCTTTAAGTCAG AAAGGATGCATTTGATCGAAACCCGGAACTTCGGAACCTCCTACTGGACGACTTCTTTAAGTCAG A G PGD Ensembl:ENSG00000142657 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:10418784..10418952;chr1:10418826..10418950 31548705,26863196 m1A-IP-seq:(High) rs1181318169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319320,Human_RBP_ID_1721111,Human_RBP_ID_3275057,Human_RBP_ID_3979145,Human_RBP_ID_8279555,Human_RBP_ID_10499634,Human_RBP_ID_17210844,Human_RBP_ID_17444320,Human_RBP_ID_17763319,Human_RBP_ID_18204434,Human_RBP_ID_18546352,Human_RBP_ID_27385169 Human_Splice_Rec_16162,Human_Splice_Rec_16163,Human_Splice_Rec_16208,Human_Splice_Rec_16209,Human_Splice_Rec_16213 RMVar_hsa_circ_21193,RMVar_hsa_circ_76698,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128997,RMVar_hsa_circ_105327,RMVar_hsa_circ_377628,RMVar_hsa_circ_128998,RMVar_hsa_circ_61009,RMVar_hsa_circ_129001,RMVar_hsa_circ_361699,RMVar_hsa_circ_90592,RMVar_hsa_circ_129004,RMVar_hsa_circ_88420,RMVar_hsa_circ_122759,RMVar_hsa_circ_129005,RMVar_hsa_circ_37014,RMVar_hsa_circ_129007,RMVar_hsa_circ_126460,RMVar_hsa_circ_129008,RMVar_hsa_circ_75897,RMVar_hsa_circ_124272,RMVar_hsa_circ_129009,RMVar_hsa_circ_118947,RMVar_hsa_circ_129010,RMVar_hsa_circ_129011 67382 RMVar_ID_67382 Human_SNP_ID_2863055 m1A Human chr1 - 10418888 10418888 10418888 AGTTTTCAACAGCTGACTTAAAGAAGTCGTCCAGTAGGAGGTTCTGAAGTTCCGGGTTTCGATCA AGTTTTCAACAGCTGACTTAAAGAAGTCGTCCGGTAGGAGGTTCTGAAGTTCCGGGTTTCGATCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10418838..10418953 26863196 MeRIP-seq:(Medium) rs906334024 Functional Loss SNV dbSNP153 33..33 33 - - - 67383 RMVar_ID_67383 Human_SNP_ID_2863238 m1A Human chr1 + 10419465 10419465 10419465 CAGTCAGCACTGGGGTCCAGGCTGGCATTCCCATGCCCTGTTTTACCACTGCCCTCTCCTTCTAT CAGTCAGCACTGGGGTCCAGGCTGGCATTCCCGTGCCCTGTTTTACCACTGCCCTCTCCTTCTAT A G PGD Ensembl:ENSG00000142657 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:10419401..10419500;chr1:10419399..10419500 26863196 MeRIP-seq:(Medium) rs185532565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_289540,Human_RBP_ID_17210845,Human_RBP_ID_27164117 Human_Splice_Rec_16164,Human_Splice_Rec_16165,Human_Splice_Rec_16210,Human_Splice_Rec_16211,Human_Splice_Rec_16214 Human_miRNA_ID_1372413,Human_miRNA_ID_2456042,Human_miRNA_ID_2460950,Human_miRNA_ID_2491895,Human_miRNA_ID_2633608,Human_miRNA_ID_2636295,Human_miRNA_ID_2694836 RMVar_hsa_circ_76698,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128997,RMVar_hsa_circ_105327,RMVar_hsa_circ_128998,RMVar_hsa_circ_61009,RMVar_hsa_circ_129001,RMVar_hsa_circ_90592,RMVar_hsa_circ_129004,RMVar_hsa_circ_88420,RMVar_hsa_circ_122759,RMVar_hsa_circ_129005,RMVar_hsa_circ_129007,RMVar_hsa_circ_126460,RMVar_hsa_circ_129008,RMVar_hsa_circ_75897,RMVar_hsa_circ_124272,RMVar_hsa_circ_129009,RMVar_hsa_circ_118947,RMVar_hsa_circ_129010,RMVar_hsa_circ_129011 67384 RMVar_ID_67384 Human_SNP_ID_2863248 m1A Human chr1 - 10419493 10419490 10419493 CTGGAAGCATCTCATGTCTGTACCCGTCATAGAAGGAGAGGGCAGTGGTAAAACAGGGCATGGGA CTGGAAGCATCTCATGTCTGTACCCGTCATAG___GAGAGGGCAGTGGTAAAACAGGGCATGGGA CCTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:10417104..10419897;chr1:10418861..10419551 32194978 MeRIP-seq:(Medium) rs753868671 Functional Loss DEL dbSNP153 33..35 33 - - - 67385 RMVar_ID_67385 Human_SNP_ID_2863346 m1A Human chr1 - 10419716 10419716 10419716 CAGGCATTGTATGACGAGGATGACACGGTGCCACCATGGCCTGTCCAGTTGGTGTGGATAAACTG CAGGCATTGTATGACGAGGATGACACGGTGCCGCCATGGCCTGTCCAGTTGGTGTGGATAAACTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10419577..10419747 26863196 MeRIP-seq:(Medium) rs1263400276 Functional Loss SNV dbSNP153 33..33 33 - - - 67386 RMVar_ID_67386 Human_SNP_ID_2863430 m1A Human chr1 + 10419977 10419977 10419977 GGGACTGACCAGGAGCTGCTCATGTGCGTGAGAGTGGGAACCATCTCCTTGCGGCAGTGGCTTCC GGGACTGACCAGGAGCTGCTCATGTGCGTGAGTGTGGGAACCATCTCCTTGCGGCAGTGGCTTCC A T PGD Ensembl:ENSG00000142657 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:10419926..10420050;chr1:10419926..10420000 32194978 MeRIP-seq:(Medium) rs1276106279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319329,Human_RBP_ID_1407266,Human_RBP_ID_3979155,Human_RBP_ID_5663839,Human_RBP_ID_8279561,Human_RBP_ID_10499664,Human_RBP_ID_23205678,Human_RBP_ID_26389478,Human_RBP_ID_26767134 Human_miRNA_ID_2619498 RMVar_hsa_circ_76698,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128997,RMVar_hsa_circ_105327,RMVar_hsa_circ_128998,RMVar_hsa_circ_129001,RMVar_hsa_circ_90592,RMVar_hsa_circ_129004,RMVar_hsa_circ_88420,RMVar_hsa_circ_122759,RMVar_hsa_circ_129005,RMVar_hsa_circ_129007,RMVar_hsa_circ_126460,RMVar_hsa_circ_129008,RMVar_hsa_circ_75897,RMVar_hsa_circ_124272,RMVar_hsa_circ_129009,RMVar_hsa_circ_127976,RMVar_hsa_circ_118947,RMVar_hsa_circ_129010,RMVar_hsa_circ_129011,RMVar_hsa_circ_129012 67387 RMVar_ID_67387 Human_SNP_ID_2866599 m1A Human chr1 + 10430536 10430536 10430536 GTCGGCCCGCAGTGATGGAGGAGGAGGCGGAGACCGAGGAGCAGCAGCGATTCTCTTACCAACAG GTCGGCCCGCAGTGATGGAGGAGGAGGCGGAGGCCGAGGAGCAGCAGCGATTCTCTTACCAACAG A G CENPS-CORT,CENPS Ensembl:ENSG00000251503,Ensembl:ENSG00000175279 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10430486..10430577 26863196 MeRIP-seq:(Medium) rs1395083986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073516 Human_Splice_Rec_16215,Human_Splice_Rec_16223,Human_Splice_Rec_16229,Human_Splice_Rec_16249,Human_Splice_Rec_16257 67388 RMVar_ID_67388 Human_SNP_ID_2870162 m1A Human chr1 + 10442653 10442653 10442653 CTCACTCCAGAACATAAAAATGGTGTGTGATCAAATGGTATATATTAGAAATTACATCTGTTGTA CTCACTCCAGAACATAAAAATGGTGTGTGATCCAATGGTATATATTAGAAATTACATCTGTTGTA A C CENPS-CORT,CENPS Ensembl:ENSG00000251503,Ensembl:ENSG00000175279 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2847337 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8026,GWAS_ID_8027,GWAS_ID_8028 67389 RMVar_ID_67389 Human_SNP_ID_2870163 m1A Human chr1 + 10442653 10442653 10442653 CTCACTCCAGAACATAAAAATGGTGTGTGATCAAATGGTATATATTAGAAATTACATCTGTTGTA CTCACTCCAGAACATAAAAATGGTGTGTGATCGAATGGTATATATTAGAAATTACATCTGTTGTA A G CENPS-CORT,CENPS Ensembl:ENSG00000251503,Ensembl:ENSG00000175279 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2847337 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8026,GWAS_ID_8027,GWAS_ID_8028 67390 RMVar_ID_67390 Human_SNP_ID_2870164 m1A Human chr1 + 10442653 10442653 10442653 CTCACTCCAGAACATAAAAATGGTGTGTGATCAAATGGTATATATTAGAAATTACATCTGTTGTA CTCACTCCAGAACATAAAAATGGTGTGTGATCTAATGGTATATATTAGAAATTACATCTGTTGTA A T CENPS-CORT,CENPS Ensembl:ENSG00000251503,Ensembl:ENSG00000175279 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2847337 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8026,GWAS_ID_8027,GWAS_ID_8028 67391 RMVar_ID_67391 Human_SNP_ID_2874372 m1A Human chr1 - 10457556 10457556 10457556 CTCTTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGTGCCCGCCACCACACCCGGCTAAGTTTT CTCTTGCCTCAGCCTCCAGAGTAGCTGGGATTGCAGGTGCCCGCCACCACACCCGGCTAAGTTTT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1172510059 Functional Loss SNV dbSNP153 33..33 33 - - - 67392 RMVar_ID_67392 Human_SNP_ID_2875079 m1A Human chr1 - 10460133 10460133 10460133 TCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCAGCTGGGATTACAGGCACGTGCCACCATGCCCG TCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCGGCTGGGATTACAGGCACGTGCCACCATGCCCG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1223842253 Functional Loss SNV dbSNP153 33..33 33 - - - 67393 RMVar_ID_67393 Human_SNP_ID_2875105 m1A Human chr1 - 10460201 10460201 10460201 TCACTCTGTCACCTAGTCTGGAGTGCAGTGGCACATTCTCGGCTCACTGCAACCCCCACCTCCCA TCACTCTGTCACCTAGTCTGGAGTGCAGTGGCGCATTCTCGGCTCACTGCAACCCCCACCTCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1290603364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26364835 67394 RMVar_ID_67394 Human_SNP_ID_2875303 m1A Human chr1 - 10460694 10460694 10460694 GAAACGTGTTTTTACTAAAAGTACAAAAAACTAGCTGGGCGTGGTGGCAGGAGCCTGTAGTCCCA GAAACGTGTTTTTACTAAAAGTACAAAAAACTGGCTGGGCGTGGTGGCAGGAGCCTGTAGTCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1413686371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664043,Human_RBP_ID_26385201 67395 RMVar_ID_67395 Human_SNP_ID_2876097 m1A Human chr1 - 10462567 10462567 10462567 ATTGTCCTTGTCCCTGTCATAAGTACCTCCCTATTGTAGATAGAAGGGAAGGAAACTGTTGACTT ATTGTCCTTGTCCCTGTCATAAGTACCTCCCTGTTGTAGATAGAAGGGAAGGAAACTGTTGACTT T C DFFA Ensembl:ENSG00000160049 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:10462563..10462763 32194978 MeRIP-seq:(Medium) rs993980865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17719875 67396 RMVar_ID_67396 Human_SNP_ID_2878691 m1A Human chr1 + 10472177 10472177 10472177 TACGCTCAAGCGCCTTAAATCTGTAAATCGCTATGCCCACTCGGACCGTTTCTGTCCCAAGCCTC TACGCTCAAGCGCCTTAAATCTGTAAATCGCTTTGCCCACTCGGACCGTTTCTGTCCCAAGCCTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:10472175..10472296 26863196 MeRIP-seq:(Medium) rs570993490 Functional Loss SNV dbSNP153 33..33 33 - - - 67397 RMVar_ID_67397 Human_SNP_ID_2878783 m1A Human chr1 + 10472433 10472432 10472434 GCTTTAGAGTCCGGATCTCGCCAGATTCTGGTACCCCGGCGTCCCCGGTCACCTCCATCCTCCAC GCTTTAGAGTCCGGATCTCGCCAGATTCTGGT__CCCGGCGTCCCCGGTCACCTCCATCCTCCAC TAC T PEX14 Ensembl:ENSG00000142655 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10472387..10472478 26863196 MeRIP-seq:(Medium) rs757575044 Functional Loss DEL dbSNP153 33..34 33 - - - 67398 RMVar_ID_67398 Human_SNP_ID_2879426 m1A Human chr1 + 10474997 10474997 10474997 AGATGGCGTCCTCGGAGCAGGCAGAGCAGCCGAGCCAGGTAAGGGGAGTGGGACTGCCCCGCTGT AGATGGCGTCCTCGGAGCAGGCAGAGCAGCCGGGCCAGGTAAGGGGAGTGGGACTGCCCCGCTGT A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:10474917..10475067 26863196 MeRIP-seq:(Medium) rs896802943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1249073,Human_RBP_ID_4073522,Human_RBP_ID_18414851,Human_RBP_ID_18967139,Human_RBP_ID_27799601 Human_Splice_Rec_16309,Human_Splice_Rec_16325 RMVar_hsa_circ_92275,RMVar_hsa_circ_129020 67399 RMVar_ID_67399 Human_SNP_ID_2879428 m1A Human chr1 + 10475001 10475001 10475001 GGCGTCCTCGGAGCAGGCAGAGCAGCCGAGCCAGGTAAGGGGAGTGGGACTGCCCCGCTGTGCGG GGCGTCCTCGGAGCAGGCAGAGCAGCCGAGCCGGGTAAGGGGAGTGGGACTGCCCCGCTGTGCGG A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10474951..10475025 26863196 MeRIP-seq:(Medium) rs1483066733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1249073,Human_RBP_ID_4073522,Human_RBP_ID_18414851,Human_RBP_ID_18967139,Human_RBP_ID_27799601 Human_Splice_Rec_16309,Human_Splice_Rec_16325 RMVar_hsa_circ_92275,RMVar_hsa_circ_129020 67400 RMVar_ID_67400 Human_SNP_ID_2884527 m1A Human chr1 - 10495255 10495255 10495255 GGAGTAGAGCTTGGCTGCAGAGAAAAATGGAAACAAAAATAAGATCACAGTGCCACCCAATGGAC GGAGTAGAGCTTGGCTGCAGAGAAAAATGGAAGCAAAAATAAGATCACAGTGCCACCCAATGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:10495251..10495325 26863196 MeRIP-seq:(Medium) rs1017223138 Functional Loss SNV dbSNP153 33..33 33 - - - 67401 RMVar_ID_67401 Human_SNP_ID_2909310 m1A Human chr1 + 10599183 10599183 10599183 TAAAGGTCTTTGCTCAGTGAAGATTCTGTTGCAGCTATGGACACTGACAAAAGGTACTCACCTGC TAAAGGTCTTTGCTCAGTGAAGATTCTGTTGCGGCTATGGACACTGACAAAAGGTACTCACCTGC A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:10599180..10599265 26863196 MeRIP-seq:(Medium) rs199609849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22632791 RMVar_hsa_circ_32108,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 67402 RMVar_ID_67402 Human_SNP_ID_2917046 m1A Human chr1 - 10630345 10630345 10630345 TAGGGACGCTAGCTCTGGCCATGCGTGGTGTCACGGTAGTCAAGACACTCAGCAAACACACCCTG TAGGGACGCTAGCTCTGGCCATGCGTGGTGTCGCGGTAGTCAAGACACTCAGCAAACACACCCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:10630208..10630509 32194978 MeRIP-seq:(Medium) rs1020803852 Functional Loss SNV dbSNP153 33..33 33 - - - 67403 RMVar_ID_67403 Human_SNP_ID_2930029 m1A Human chr1 - 10672210 10672210 10672210 TTATAGTGCGGAGGGGAGGGGGTGGCGGGGGGAGGGGGGAGAAGGTTAAACAGTATTTACAGCTC TTATAGTGCGGAGGGGAGGGGGTGGCGGGGGGGGGGGGGAGAAGGTTAAACAGTATTTACAGCTC T C CASZ1 Ensembl:ENSG00000130940 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:10672201..10672250 26863196 MeRIP-seq:(Medium) rs1202580993 Functional Loss SNV dbSNP153 33..33 33 - - - 67404 RMVar_ID_67404 Human_SNP_ID_2936026 m1A Human chr1 + 10694494 10694494 10694494 GCGGGCGGGCGGGCGCGGCCGGGGGCGCTGCCAGGCGCCGCGGTGATTGGCAGGGCGGCCGCGGC GCGGGCGGGCGGGCGCGGCCGGGGGCGCTGCCGGGCGCCGCGGTGATTGGCAGGGCGGCCGCGGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:10694491..10694617 26863196 MeRIP-seq:(Medium) rs929623669 Functional Loss SNV dbSNP153 33..33 33 - - - 67405 RMVar_ID_67405 Human_SNP_ID_2936056 m1A Human chr1 + 10694562 10694562 10694562 GCCTCCTCGGCCCGGCCCGCGCCGGCCCCGGCAGGTGAAAGAGCAGAGCGCGGCCCCGCCGCCGC GCCTCCTCGGCCCGGCCCGCGCCGGCCCCGGCCGGTGAAAGAGCAGAGCGCGGCCCCGCCGCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:10694547..10694621 26863196 MeRIP-seq:(Medium) rs1340682783 Functional Loss SNV dbSNP153 33..33 33 - - - 67406 RMVar_ID_67406 Human_SNP_ID_3021504 m1A Human chr1 - 11012709 11012709 11012709 GCTAGGCCGCTGCTGGGAAGCCCGACAGGGACACCGAAGCAGCGACGGACCCAAGCGCAGCCCAG GCTAGGCCGCTGCTGGGAAGCCCGACAGGGACGCCGAAGCAGCGACGGACCCAAGCGCAGCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:11012651..11012790;chr1:11012651..11013900 26863196 MeRIP-seq:(Medium) rs1038639698 Functional Loss SNV dbSNP153 33..33 33 - - - 67407 RMVar_ID_67407 Human_SNP_ID_3021507 m1A Human chr1 - 11012715 11012715 11012715 TCACCCGCTAGGCCGCTGCTGGGAAGCCCGACAGGGACACCGAAGCAGCGACGGACCCAAGCGCA TCACCCGCTAGGCCGCTGCTGGGAAGCCCGACCGGGACACCGAAGCAGCGACGGACCCAAGCGCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:11012651..11012802 26863196 MeRIP-seq:(Medium) rs1032991464 Functional Loss SNV dbSNP153 33..33 33 - - - 67408 RMVar_ID_67408 Human_SNP_ID_3021520 m1A Human chr1 - 11012745 11012745 11012745 ACGGCGTCCTCAGTGAGAAGGCTCCGCGACTCACCCGCTAGGCCGCTGCTGGGAAGCCCGACAGG ACGGCGTCCTCAGTGAGAAGGCTCCGCGACTCTCCCGCTAGGCCGCTGCTGGGAAGCCCGACAGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:11012651..11013781 26863410 MeRIP-seq:(Medium) rs113859301 Functional Loss SNV dbSNP153 33..33 33 - - - 67409 RMVar_ID_67409 Human_SNP_ID_3024508 m1A Human chr1 + 11022226 11022226 11022226 CTAAGCACAATAGCAATAGACAGTTAGAAAGAAGTGGAAGATTTGGTGGTAATCCAGGTGGCTTT CTAAGCACAATAGCAATAGACAGTTAGAAAGATGTGGAAGATTTGGTGGTAATCCAGGTGGCTTT A T AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11022176..11022442 26863196 MeRIP-seq:(Medium) rs756083911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1721650,Human_RBP_ID_3275895,Human_RBP_ID_8953660,Human_RBP_ID_10512723,Human_RBP_ID_23321828 Human_Splice_Rec_16533,Human_Splice_Rec_16547,Human_Splice_Rec_16611,Human_Splice_Rec_16621,Human_Splice_Rec_16645,Human_Splice_Rec_16655,Human_Splice_Rec_16663,Human_Splice_Rec_16671,Human_Splice_Rec_16681,Human_Splice_Rec_16689,Human_Splice_Rec_16697,Human_Splice_Rec_16705,Human_Splice_Rec_16715,Human_Splice_Rec_16753,Human_Splice_Rec_16763,Human_Splice_Rec_16769 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 67410 RMVar_ID_67410 Human_SNP_ID_3034789 m1A Human chr1 + 11054700 11054697 11054701 TTGGAGGTGGAACGCCAGAGAGACAGACACACAGACAGTCCGCCCAGCAGGGCAGGCCGGGCAGC TTGGAGGTGGAACGCCAGAGAGACAGACAC____ACAGTCCGCCCAGCAGGGCAGGCCGGGCAGC CACAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:11054649..11054812 26863196 MeRIP-seq:(Medium) rs1418041131 Functional Loss DEL dbSNP153 31..34 33 - - - 67411 RMVar_ID_67411 Human_SNP_ID_3034831 m1A Human chr1 - 11054827 11054827 11054827 GGCGCCACCACTGATGCCACCCAGGACCTCGGACCTTGGAGCCTGCGGGGTGCCTCGGCCCCTCC GGCGCCACCACTGATGCCACCCAGGACCTCGGGCCTTGGAGCCTGCGGGGTGCCTCGGCCCCTCC T C SRM Ensembl:ENSG00000116649 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:11054601..11055050 26863196 MeRIP-seq:(Medium) rs774308445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320815,Human_RBP_ID_1408139,Human_RBP_ID_3981886,Human_RBP_ID_9319707,Human_RBP_ID_17646854,Human_RBP_ID_22871707,Human_RBP_ID_26797661,Human_RBP_ID_26837342,Human_RBP_ID_27152666,Human_RBP_ID_27385746,Human_RBP_ID_27554154 Human_Splice_Rec_16814,Human_Splice_Rec_16828 RMVar_hsa_circ_82027,RMVar_hsa_circ_107634,RMVar_hsa_circ_114867,RMVar_hsa_circ_109128,RMVar_hsa_circ_92969,RMVar_hsa_circ_103282,RMVar_hsa_circ_84220,RMVar_hsa_circ_129034,RMVar_hsa_circ_129036,RMVar_hsa_circ_129038,RMVar_hsa_circ_75943,RMVar_hsa_circ_129037,RMVar_hsa_circ_129035,RMVar_hsa_circ_129032,RMVar_hsa_circ_129033,RMVar_hsa_circ_129031 67412 RMVar_ID_67412 Human_SNP_ID_3035514 m1A Human chr1 - 11056756 11056756 11056756 GGCCCAGACTGGTCCCTCCCATCCCCTCCAGGATGTCATCCAAGTCTCCAAGAAGTTCCTGCCAG GGCCCAGACTGGTCCCTCCCATCCCCTCCAGGGTGTCATCCAAGTCTCCAAGAAGTTCCTGCCAG T C SRM Ensembl:ENSG00000116649 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:11056726..11056775 26863196 MeRIP-seq:(Medium) rs1374579948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16820,Human_Splice_Rec_16832,Human_Splice_Rec_16840,Human_Splice_Rec_16846 Human_miRNA_ID_2720944 RMVar_hsa_circ_82027,RMVar_hsa_circ_109128,RMVar_hsa_circ_84220,RMVar_hsa_circ_129034,RMVar_hsa_circ_75943,RMVar_hsa_circ_129032,RMVar_hsa_circ_129033,RMVar_hsa_circ_129031,RMVar_hsa_circ_129039,RMVar_hsa_circ_125542 67413 RMVar_ID_67413 Human_SNP_ID_3036176 m1A Human chr1 - 11058843 11058843 11058843 CGGAGATGGAGGTGTCCTGCGGGAGGTGGTGAAGCACCCCTCCGTGGAGTCCGTGGTCCAGTGTG CGGAGATGGAGGTGTCCTGCGGGAGGTGGTGAGGCACCCCTCCGTGGAGTCCGTGGTCCAGTGTG T C SRM Ensembl:ENSG00000116649 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:11056750..11059385 32194978 MeRIP-seq:(Medium) rs774724271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320844,Human_RBP_ID_3981915,Human_RBP_ID_8240048,Human_RBP_ID_9270857,Human_RBP_ID_17720897,Human_RBP_ID_18186819,Human_RBP_ID_18547279,Human_RBP_ID_18967143,Human_RBP_ID_23322355,Human_RBP_ID_26837357,Human_RBP_ID_27164848,Human_RBP_ID_27385757 Human_Splice_Rec_16818,Human_Splice_Rec_16819,Human_Splice_Rec_16838,Human_Splice_Rec_16839,Human_Splice_Rec_16844,Human_Splice_Rec_16845 Human_miRNA_ID_2152645,Human_miRNA_ID_2170591,Human_miRNA_ID_2800516,Human_miRNA_ID_3008644 RMVar_hsa_circ_82027,RMVar_hsa_circ_109128,RMVar_hsa_circ_75943,RMVar_hsa_circ_129032,RMVar_hsa_circ_129033,RMVar_hsa_circ_129031,RMVar_hsa_circ_129040,RMVar_hsa_circ_129039,RMVar_hsa_circ_125542,RMVar_hsa_circ_119291 67414 RMVar_ID_67414 Human_SNP_ID_3036544 m1A Human chr1 + 11059897 11059897 11059897 GGCTGCAGGTCTCGCGGAACCAGCCCTCGCGGATGGCGGCGGGGCCGGAGGCGGCGGGGCCGTCG GGCTGCAGGTCTCGCGGAACCAGCCCTCGCGGGTGGCGGCGGGGCCGGAGGCGGCGGGGCCGTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11059755..11060025 26863196 MeRIP-seq:(Medium) rs1208264105 Functional Loss SNV dbSNP153 33..33 33 - - - 67415 RMVar_ID_67415 Human_SNP_ID_3036773 m1A Human chr1 + 11060381 11060381 11060381 GGGAGGCACCGAGGGCCTCGAGGGGCTGCGGGACTCGGGCTTGGTGTGGAGGGCAAGAGCGCTGC GGGAGGCACCGAGGGCCTCGAGGGGCTGCGGGGCTCGGGCTTGGTGTGGAGGGCAAGAGCGCTGC A G lnc-TARDBP-5,lnc-TARDBP-5:2,lnc-TARDBP-5:3,lnc-TARDBP-5:4,lnc-TARDBP-5:5,lnc-TARDBP-5:6 RNACentral:URS0000D597D9,RNACentral:URS0000D57118,RNACentral:URS00008C329B,RNACentral:URS0000D5DBDB,RNACentral:URS0000D58D0A,RNACentral:URS0000D5BAE0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:11060347..11060461;chr1:11060334..11060455 26863196 MeRIP-seq:(Medium) rs1159703844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3981955 67416 RMVar_ID_67416 Human_SNP_ID_3039327 m1A Human chr1 - 11069686 11069686 11069686 GCAAAGAAGAGAGAGCGAGCAACAAGCGACCCAAGGACCACAGAACAGAAACAAGAGAAGAAACG GCAAAGAAGAGAGAGCGAGCAACAAGCGACCCGAGGACCACAGAACAGAAACAAGAGAAGAAACG T C EXOSC10 Ensembl:ENSG00000171824 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11069638..11069769 26863196 MeRIP-seq:(Medium) rs749557592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16886,Human_Splice_Rec_16934,Human_Splice_Rec_16958,Human_Splice_Rec_16970,Human_Splice_Rec_16976 RMVar_hsa_circ_54801,RMVar_hsa_circ_289591 67417 RMVar_ID_67417 Human_SNP_ID_3039332 m1A Human chr1 - 11069694 11069694 11069694 AAAATGCTGCAAAGAAGAGAGAGCGAGCAACAAGCGACCCAAGGACCACAGAACAGAAACAAGAG AAAATGCTGCAAAGAAGAGAGAGCGAGCAACACGCGACCCAAGGACCACAGAACAGAAACAAGAG T G EXOSC10 Ensembl:ENSG00000171824 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11069643..11069769 26863196 MeRIP-seq:(Medium) rs1375970416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16886,Human_Splice_Rec_16934,Human_Splice_Rec_16958,Human_Splice_Rec_16970,Human_Splice_Rec_16976 RMVar_hsa_circ_54801,RMVar_hsa_circ_289591 67418 RMVar_ID_67418 Human_SNP_ID_3039941 m1A Human chr1 - 11071733 11071733 11071733 GGCTAGTTCACTGGGCATGCTGAGCAGCAGCAAGTGGGCCTGCATGAGCAGAGCGGGTAGAGAAG GGCTAGTTCACTGGGCATGCTGAGCAGCAGCACGTGGGCCTGCATGAGCAGAGCGGGTAGAGAAG T G EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11071731..11071882 26863196 MeRIP-seq:(Medium) rs1025573294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10516601 RMVar_hsa_circ_4265,RMVar_hsa_circ_54801,RMVar_hsa_circ_289591,RMVar_hsa_circ_278266,RMVar_hsa_circ_298600,RMVar_hsa_circ_367755,RMVar_hsa_circ_83091,RMVar_hsa_circ_129041,RMVar_hsa_circ_129042,RMVar_hsa_circ_129043 67419 RMVar_ID_67419 Human_SNP_ID_3041562 m1A Human chr1 + 11077440 11077440 11077440 GCAGTCGTGAGGTCCAAAGAGAACATTCTCCAATCTCTGCATTAAAAGACACCAGCAGGCTGGCA GCAGTCGTGAGGTCCAAAGAGAACATTCTCCAGTCTCTGCATTAAAAGACACCAGCAGGCTGGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11077355..11077455 32194978 MeRIP-seq:(Medium) rs1553165516 Functional Loss SNV dbSNP153 33..33 33 - - - 67420 RMVar_ID_67420 Human_SNP_ID_3041563 m1A Human chr1 + 11077440 11077440 11077440 GCAGTCGTGAGGTCCAAAGAGAACATTCTCCAATCTCTGCATTAAAAGACACCAGCAGGCTGGCA GCAGTCGTGAGGTCCAAAGAGAACATTCTCCATTCTCTGCATTAAAAGACACCAGCAGGCTGGCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11077355..11077455 32194978 MeRIP-seq:(Medium) rs1553165516 Functional Loss SNV dbSNP153 33..33 33 - - - 67421 RMVar_ID_67421 Human_SNP_ID_3042764 m1A Human chr1 - 11081106 11081106 11081106 GGGCAGCCGGTGCAGCTGCAGGTGGTGTGGCAACGGAGCAGGGACATCTGCCTCAAGGTACACCT GGGCAGCCGGTGCAGCTGCAGGTGGTGTGGCAGCGGAGCAGGGACATCTGCCTCAAGGTACACCT T C EXOSC10 Ensembl:ENSG00000171824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11081076..11082760 32194978 MeRIP-seq:(Medium) rs1391452316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222908,Human_RBP_ID_802180,Human_RBP_ID_860921,Human_RBP_ID_18547325,Human_RBP_ID_22426888,Human_RBP_ID_22871708 Human_Splice_Rec_16867,Human_Splice_Rec_16913,Human_Splice_Rec_16941,Human_Splice_Rec_16993 RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_2027,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_315026,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532,RMVar_hsa_circ_30028,RMVar_hsa_circ_129057,RMVar_hsa_circ_15609,RMVar_hsa_circ_315325,RMVar_hsa_circ_94386,RMVar_hsa_circ_129058,RMVar_hsa_circ_5541,RMVar_hsa_circ_129059 67422 RMVar_ID_67422 Human_SNP_ID_3085509 m1A Human chr1 - 11251220 11251220 11251220 GCAGTAGCAGCTCCCCTACCATGGCTGAGCAGAGTGAGCAGGAGAAGTGTGTGGGGATATGGGGT GCAGTAGCAGCTCCCCTACCATGGCTGAGCAGGGTGAGCAGGAGAAGTGTGTGGGGATATGGGGT T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11251218..11251289 26863196 MeRIP-seq:(Medium) rs1208907335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5671463 RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129083,RMVar_hsa_circ_129086,RMVar_hsa_circ_108487,RMVar_hsa_circ_129088,RMVar_hsa_circ_103330,RMVar_hsa_circ_129098,RMVar_hsa_circ_98102,RMVar_hsa_circ_118210,RMVar_hsa_circ_129102,RMVar_hsa_circ_121856,RMVar_hsa_circ_129103,RMVar_hsa_circ_129105,RMVar_hsa_circ_91108,RMVar_hsa_circ_129113,RMVar_hsa_circ_123573,RMVar_hsa_circ_129116,RMVar_hsa_circ_111428,RMVar_hsa_circ_129120,RMVar_hsa_circ_84113,RMVar_hsa_circ_129128,RMVar_hsa_circ_103705,RMVar_hsa_circ_80346,RMVar_hsa_circ_85076,RMVar_hsa_circ_129137,RMVar_hsa_circ_129138,RMVar_hsa_circ_20879,RMVar_hsa_circ_129141,RMVar_hsa_circ_114321,RMVar_hsa_circ_120662,RMVar_hsa_circ_129144,RMVar_hsa_circ_129145,RMVar_hsa_circ_91544,RMVar_hsa_circ_129146,RMVar_hsa_circ_129148,RMVar_hsa_circ_105059,RMVar_hsa_circ_97079,RMVar_hsa_circ_99845,RMVar_hsa_circ_116693,RMVar_hsa_circ_129151,RMVar_hsa_circ_129152,RMVar_hsa_circ_45471,RMVar_hsa_circ_129154 67423 RMVar_ID_67423 Human_SNP_ID_3086066 m1A Human chr1 - 11253402 11253402 11253402 AATTAATAGGCCCACGGTTCACAGTAAACACGAGCTTTCACAGGGGTAAACATTGGAAGTATGCA AATTAATAGGCCCACGGTTCACAGTAAACACGGGCTTTCACAGGGGTAAACATTGGAAGTATGCA T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11253400..11253634 26863196 MeRIP-seq:(Medium) rs1018182341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129083,RMVar_hsa_circ_129086,RMVar_hsa_circ_108487,RMVar_hsa_circ_129088,RMVar_hsa_circ_103330,RMVar_hsa_circ_129098,RMVar_hsa_circ_98102,RMVar_hsa_circ_118210,RMVar_hsa_circ_129102,RMVar_hsa_circ_121856,RMVar_hsa_circ_129103,RMVar_hsa_circ_129105,RMVar_hsa_circ_91108,RMVar_hsa_circ_129113,RMVar_hsa_circ_123573,RMVar_hsa_circ_129116,RMVar_hsa_circ_111428,RMVar_hsa_circ_129120,RMVar_hsa_circ_84113,RMVar_hsa_circ_129128,RMVar_hsa_circ_103705,RMVar_hsa_circ_80346,RMVar_hsa_circ_85076,RMVar_hsa_circ_129137,RMVar_hsa_circ_129138,RMVar_hsa_circ_20879,RMVar_hsa_circ_129141,RMVar_hsa_circ_114321,RMVar_hsa_circ_120662,RMVar_hsa_circ_129144,RMVar_hsa_circ_129145,RMVar_hsa_circ_91544,RMVar_hsa_circ_129146,RMVar_hsa_circ_129148,RMVar_hsa_circ_105059,RMVar_hsa_circ_97079,RMVar_hsa_circ_99845,RMVar_hsa_circ_116693,RMVar_hsa_circ_129151,RMVar_hsa_circ_129152,RMVar_hsa_circ_45471,RMVar_hsa_circ_129154 67424 RMVar_ID_67424 Human_SNP_ID_3087689 m1A Human chr1 + 11259356 11259356 11259356 AGGCCACTGGCAAACTGCTGCAGGACGCTCACATTGCTAGATGTGGTGGCAGCGGTGGTGGCGGC AGGCCACTGGCAAACTGCTGCAGGACGCTCACCTTGCTAGATGTGGTGGCAGCGGTGGTGGCGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:11259306..11259479;chr1:11259306..11259461 26863196 MeRIP-seq:(Medium) rs766795299 Functional Loss SNV dbSNP153 33..33 33 - - - 67425 RMVar_ID_67425 Human_SNP_ID_3087690 m1A Human chr1 + 11259356 11259356 11259356 AGGCCACTGGCAAACTGCTGCAGGACGCTCACATTGCTAGATGTGGTGGCAGCGGTGGTGGCGGC AGGCCACTGGCAAACTGCTGCAGGACGCTCACGTTGCTAGATGTGGTGGCAGCGGTGGTGGCGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:11259306..11259479;chr1:11259306..11259461 26863196 MeRIP-seq:(Medium) rs766795299 Functional Loss SNV dbSNP153 33..33 33 - - - 67426 RMVar_ID_67426 Human_SNP_ID_3092367 m1A Human chr1 + 11275922 11275920 11275922 GAGCAGCAAGAAGTCCAGTGTGTGAATGAAGGAGAGAGTAAAGAGAGGTAAAGTAAGAGAAGTAC GAGCAGCAAGAAGTCCAGTGTGTGAATGAAG__GAGAGTAAAGAGAGGTAAAGTAAGAGAAGTAC GGA G UBIAD1 Ensembl:ENSG00000120942 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11275797..11276289 26863196 MeRIP-seq:(Medium) rs368463936 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_81469,RMVar_hsa_circ_129157 67427 RMVar_ID_67427 Human_SNP_ID_3190538 m1A Human chr1 - 11654632 11654632 11654632 TCCTCCCAGCAGTCCCCCAGGAGCGAGCTGCGAGATGCCCCAAATCGGACCCCTCCCCAGTTGGA TCCTCCCAGCAGTCCCCCAGGAGCGAGCTGCGTGATGCCCCAAATCGGACCCCTCCCCAGTTGGA T A FBXO2 Ensembl:ENSG00000116661 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11654530..11654765 26863196 MeRIP-seq:(Medium) rs80296647 Functional Loss SNV dbSNP153 33..33 33 - - - 67428 RMVar_ID_67428 Human_SNP_ID_3190539 m1A Human chr1 - 11654632 11654632 11654632 TCCTCCCAGCAGTCCCCCAGGAGCGAGCTGCGAGATGCCCCAAATCGGACCCCTCCCCAGTTGGA TCCTCCCAGCAGTCCCCCAGGAGCGAGCTGCGGGATGCCCCAAATCGGACCCCTCCCCAGTTGGA T C FBXO2 Ensembl:ENSG00000116661 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11654530..11654765 26863196 MeRIP-seq:(Medium) rs80296647 Functional Loss SNV dbSNP153 33..33 33 - - - 67429 RMVar_ID_67429 Human_SNP_ID_3192552 m1A Human chr1 - 11661208 11661208 11661208 GTTGGTGACCCTCGGGCCGTACCAGCCGGCCCAGTAATGAGTGTCCACGCCGCCGTGCTGAAACC GTTGGTGACCCTCGGGCCGTACCAGCCGGCCCGGTAATGAGTGTCCACGCCGCCGTGCTGAAACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11661159..11661278 26863196 MeRIP-seq:(Medium) rs1385217112 Functional Loss SNV dbSNP153 33..33 33 - - - 67430 RMVar_ID_67430 Human_SNP_ID_3196821 m1A Human chr1 - 11674620 11674620 11674620 GCCCCAGCCCGGGGCCGCTCAGGTCTGCTTGGAGGATGCCTCCCCCAGGAGGGCAGTGAGGGATG GCCCCAGCCCGGGGCCGCTCAGGTCTGCTTGGGGGATGCCTCCCCCAGGAGGGCAGTGAGGGATG T C MAD2L2 Ensembl:ENSG00000116670 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11674569..11674731 26863196 MeRIP-seq:(Medium) rs1413052797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221427,Human_RBP_ID_322943,Human_RBP_ID_1074309,Human_RBP_ID_4075145,Human_RBP_ID_5108434,Human_RBP_ID_5136597,Human_RBP_ID_8282286,Human_RBP_ID_8954574,Human_RBP_ID_17646098,Human_RBP_ID_17722655,Human_RBP_ID_18186824,Human_RBP_ID_26366712 Human_miRNA_ID_2038245,Human_miRNA_ID_2473839,Human_miRNA_ID_2959625,Human_miRNA_ID_3017225 RMVar_hsa_circ_92593,RMVar_hsa_circ_129171 67431 RMVar_ID_67431 Human_SNP_ID_3196851 m1A Human chr1 + 11674725 11674725 11674725 AGGGCAGCCATGCAGCACTGCCCTAGGCGGGGATCCCCCAAAGTCTGACAGTTTGGGCATCAGTG AGGGCAGCCATGCAGCACTGCCCTAGGCGGGGTTCCCCCAAAGTCTGACAGTTTGGGCATCAGTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:11674529..11674825 32194978 MeRIP-seq:(Medium) rs1233402293 Functional Loss SNV dbSNP153 33..33 33 - - - 67432 RMVar_ID_67432 Human_SNP_ID_3198521 m1A Human chr1 - 11680462 11680439 11680462 CACCGGCTTGTGCCCCCCTGCAGTGGTGGCCGATGTGCTCTGCGAGTTCCTGGAGGTGGCTGTGC CACCGGCTTGTGCCCCCCTGCAGTGGTGGCCG_______________________GTGGCTGTGC CCTCCAGGAACTCGCAGAGCACAT C MAD2L2 Ensembl:ENSG00000116670 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11680416..11680517 32194978 MeRIP-seq:(Medium) rs1415247987 Functional Loss DEL dbSNP153 33..55 33 - - - Human_RBP_ID_322961,Human_RBP_ID_746294,Human_RBP_ID_4072524,Human_RBP_ID_17762333 Human_Splice_Rec_17450,Human_Splice_Rec_17470,Human_Splice_Rec_17486,Human_Splice_Rec_17502,Human_Splice_Rec_17518,Human_Splice_Rec_17542,Human_Splice_Rec_17554,Human_Splice_Rec_17564 RMVar_hsa_circ_336315,RMVar_hsa_circ_18724 67433 RMVar_ID_67433 Human_SNP_ID_3198671 m1A Human chr1 + 11680765 11680765 11680765 CGCACAGGCTCAGGGCAGCTGGAAGAACCTCCACCCCCACGCTGGCGTCCGTGCTTGGGGGCATC CGCACAGGCTCAGGGCAGCTGGAAGAACCTCCCCCCCCACGCTGGCGTCCGTGCTTGGGGGCATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11680764..11680913 26863196 MeRIP-seq:(Medium) rs559477212 Functional Loss SNV dbSNP153 33..33 33 - - - 67434 RMVar_ID_67434 Human_SNP_ID_3198759 m1A Human chr1 - 11681021 11681020 11681021 CCGAGCGCAGAGCCGGTACTGGGGGAGGGGAGAGGGGGCGGGATTCCCGCCGGGAGGGATCCGGC CCGAGCGCAGAGCCGGTACTGGGGGAGGGGAG_GGGGGCGGGATTCCCGCCGGGAGGGATCCGGC CT C MAD2L2 Ensembl:ENSG00000116670 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11681012..11681112 32194978 MeRIP-seq:(Medium) rs753497816 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5311525,Human_RBP_ID_8940110,Human_RBP_ID_19033905 67435 RMVar_ID_67435 Human_SNP_ID_3215315 m1A Human chr1 - 11746990 11746990 11746990 CCAGCCACTGCCCTGTGCGGCGGGCGCCCTCTACCCTGACACCTGGCCCTCCTTTTGTCATTCAC CCAGCCACTGCCCTGTGCGGCGGGCGCCCTCTCCCCTGACACCTGGCCCTCCTTTTGTCATTCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11746986..11747069 26863196 MeRIP-seq:(Medium) rs1234210636 Functional Loss SNV dbSNP153 33..33 33 - - - 67436 RMVar_ID_67436 Human_SNP_ID_3232385 m1A Human chr1 + 11805806 11805806 11805806 AGAGGCAGGCCGGCCTCCAGCGCTCCCCGCCCACAAGCACGTCCTTGCCCCCGGGAGGTTGTTTG AGAGGCAGGCCGGCCTCCAGCGCTCCCCGCCCGCAAGCACGTCCTTGCCCCCGGGAGGTTGTTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11805768..11805915 26863196 MeRIP-seq:(Medium) rs929956993 Functional Loss SNV dbSNP153 33..33 33 - - - 67437 RMVar_ID_67437 Human_SNP_ID_3235192 m1A Human chr1 - 11815799 11815799 11815799 AGTTGAGTCAAAAGGTCATGTCAGGTGAGAAGACCTGCAAAGGGACAAACCTCTGGGTTCCTGCT AGTTGAGTCAAAAGGTCATGTCAGGTGAGAAGGCCTGCAAAGGGACAAACCTCTGGGTTCCTGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11815794..11815866 26863196 MeRIP-seq:(Medium) rs1204955638 Functional Loss SNV dbSNP153 33..33 33 - - - 67438 RMVar_ID_67438 Human_SNP_ID_3247889 m1A Human chr1 - 11858870 11858855 11858870 CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGAAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG CGGACGCATCGCAGCAGCAGCAGCAGCAGCAG_______________CCTCCGCAGTCCCTCCAG GCTGCTGCTGCTGCTT G NPPB Ensembl:ENSG00000120937 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11858823..11858922 26863196 MeRIP-seq:(Medium) rs1312097139 Functional Loss DEL dbSNP153 33..47 33 - - - 67439 RMVar_ID_67439 Human_SNP_ID_3247895 m1A Human chr1 - 11858870 11858858 11858870 CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGAAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG CGGACGCATCGCAGCAGCAGCAGCAGCAGCAG____________CAGCCTCCGCAGTCCCTCCAG GCTGCTGCTGCTT G NPPB Ensembl:ENSG00000120937 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11858823..11858922 26863196 MeRIP-seq:(Medium) rs571539855 Functional Loss DEL dbSNP153 33..44 33 - - - 67440 RMVar_ID_67440 Human_SNP_ID_3247906 m1A Human chr1 - 11858870 11858870 11858870 CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGAAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG T G NPPB Ensembl:ENSG00000120937 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11858823..11858922 26863196 MeRIP-seq:(Medium) rs1000622449 Functional Loss SNV dbSNP153 33..33 33 - - - 67441 RMVar_ID_67441 Human_SNP_ID_3263076 m1A Human chr1 - 11909598 11909598 11909598 TCCTACGTAGCTTGAATGGGGCTTTGAGTCGCATGGCGGGGCACGGCGGGGCACGGCGGGGCACG TCCTACGTAGCTTGAATGGGGCTTTGAGTCGCGTGGCGGGGCACGGCGGGGCACGGCGGGGCACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:11909549..11909648;chr1:11909548..11909697 26863196 MeRIP-seq:(Medium) rs1193000425 Functional Loss SNV dbSNP153 33..33 33 - - - 67442 RMVar_ID_67442 Human_SNP_ID_3267707 m1A Human chr1 + 11925297 11925297 11925297 TGTCCAAGAGCTCCAGCATTTCCTTCCGTGCCAAGTCCTGCAGCGCCTTGAGCTCCTTGGCTGCT TGTCCAAGAGCTCCAGCATTTCCTTCCGTGCCCAGTCCTGCAGCGCCTTGAGCTCCTTGGCTGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11925248..11925400 26863196 MeRIP-seq:(Medium) rs758478693 Functional Loss SNV dbSNP153 33..33 33 - - - 67443 RMVar_ID_67443 Human_SNP_ID_3268019 m1A Human chr1 - 11925974 11925974 11925974 GAGCGCGGTGAGGTGGTACCGCTGGGTCCTGGAGTGCCGGCCCTGGTGGCCAACGGCTTCCTGGC GAGCGCGGTGAGGTGGTACCGCTGGGTCCTGGGGTGCCGGCCCTGGTGGCCAACGGCTTCCTGGC T C KIAA2013 Ensembl:ENSG00000116685 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:11925880..11925981 26863410 MeRIP-seq:(Medium) rs1313823470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072528,Human_RBP_ID_8753504,Human_RBP_ID_9318595,Human_RBP_ID_18468442,Human_RBP_ID_22428070,Human_RBP_ID_27554256 67444 RMVar_ID_67444 Human_SNP_ID_3268160 m1A Human chr1 + 11926296 11926296 11926296 CGAGGGCGGCCGCCGGGCCCGCCGCCCAGCCCACCGGCCCGGCCGCCCGCGCCTCACTGCCCGGC CGAGGGCGGCCGCCGGGCCCGCCGCCCAGCCCGCCGGCCCGGCCGCCCGCGCCTCACTGCCCGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:11926201..11926425 26863196 MeRIP-seq:(Medium) rs1174126024 Functional Loss SNV dbSNP153 33..33 33 - - - 67445 RMVar_ID_67445 Human_SNP_ID_3268179 m1A Human chr1 + 11926362 11926354 11926363 CGGACCGCGGCGCCCACCCCGGCCCCCGCCGCAACCGCCGCAGCAGCCGCCACCCCTGCTTCCTC CGGACCGCGGCGCCCACCCCGGCCC_________CCGCCGCAGCAGCCGCCACCCCTGCTTCCTC CCCGCCGCAA C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr1:11926234..11926382;chr1:11926273..11926377 26863196,26863410 MeRIP-seq:(Medium) rs949755787 Functional Loss DEL dbSNP153 26..34 33 - - - 67446 RMVar_ID_67446 Human_SNP_ID_3270524 m1A Human chr1 + 11934853 11934853 11934853 GCTGGCCGAAGCGAAGGGCGACGCCAAGCCGGAGGGTGAGGGAGCGAAGGCCGGGGGCGGGAGCG GCTGGCCGAAGCGAAGGGCGACGCCAAGCCGGCGGGTGAGGGAGCGAAGGCCGGGGGCGGGAGCG A C PLOD1 Ensembl:ENSG00000083444 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:11934726..11935027 26863196 MeRIP-seq:(Medium) rs774044489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073559,Human_RBP_ID_19036735 Human_Splice_Rec_18401,Human_Splice_Rec_18411,Human_Splice_Rec_18447,Human_Splice_Rec_18457 RMVar_hsa_circ_77725,RMVar_hsa_circ_126101,RMVar_hsa_circ_129208,RMVar_hsa_circ_129209 67447 RMVar_ID_67447 Human_SNP_ID_3273811 m1A Human chr1 - 11947988 11947988 11947988 ATCCCTCGGTCTCCTTAGTGGCCACCGTGAGGACTAAAAGGTTGTCTGCAGACAGAGGAGGGTAT ATCCCTCGGTCTCCTTAGTGGCCACCGTGAGGGCTAAAAGGTTGTCTGCAGACAGAGGAGGGTAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:11947976..11948000 26863196 MeRIP-seq:(Medium) rs777178486 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_271 67448 RMVar_ID_67448 Human_SNP_ID_3274508 m1A Human chr1 - 11950370 11950367 11950370 CTTCTTCAGGAGCTCCCGGGGCCCCGATGCAAACAGCACGTCATAGCTGTGGCCAGAGCAGCGAG CTTCTTCAGGAGCTCCCGGGGCCCCGATGCAA___GCACGTCATAGCTGTGGCCAGAGCAGCGAG CTGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:11950351..11950400 26863196 MeRIP-seq:(Medium) rs770511543 Functional Loss DEL dbSNP153 33..35 33 - - - 67449 RMVar_ID_67449 Human_SNP_ID_3277512 m1A Human chr1 - 11960726 11960726 11960726 TTCCTGGCATCTGCATTCGCCATCCGCACCTCAGGGCCCACCAGCTTCACAGACTGGTACTCGCT TTCCTGGCATCTGCATTCGCCATCCGCACCTCGGGGCCCACCAGCTTCACAGACTGGTACTCGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:11960676..11960750 32194978 MeRIP-seq:(Medium) rs1324180968 Functional Loss SNV dbSNP153 33..33 33 - - - 67450 RMVar_ID_67450 Human_SNP_ID_3279447 m1A Human chr1 + 11967087 11967087 11967087 GGAGCACTTTGGCCAGTGGTCTCTGGGCAACAACAAGGTGGGACCCTGATGCCTGGGCTGGGGCC GGAGCACTTTGGCCAGTGGTCTCTGGGCAACATCAAGGTGGGACCCTGATGCCTGGGCTGGGGCC A T PLOD1 Ensembl:ENSG00000083444 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11967037..11967125 26863196 MeRIP-seq:(Medium) rs1243061191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_860585,Human_RBP_ID_17763350,Human_RBP_ID_18187526,Human_RBP_ID_18468454,Human_RBP_ID_22428100 Human_Splice_Rec_18441,Human_Splice_Rec_18483 RMVar_hsa_circ_9361,RMVar_hsa_circ_81636,RMVar_hsa_circ_77725,RMVar_hsa_circ_129208,RMVar_hsa_circ_79810,RMVar_hsa_circ_129211,RMVar_hsa_circ_101170,RMVar_hsa_circ_129215,RMVar_hsa_circ_112486,RMVar_hsa_circ_129218,RMVar_hsa_circ_129220,RMVar_hsa_circ_87402,RMVar_hsa_circ_129219,RMVar_hsa_circ_86782,RMVar_hsa_circ_129221,RMVar_hsa_circ_116125,RMVar_hsa_circ_129225,RMVar_hsa_circ_91464,RMVar_hsa_circ_115355,RMVar_hsa_circ_121083,RMVar_hsa_circ_129230,RMVar_hsa_circ_129232,RMVar_hsa_circ_120563,RMVar_hsa_circ_129233,RMVar_hsa_circ_129234 67451 RMVar_ID_67451 Human_SNP_ID_3281756 m1A Human chr1 + 11974822 11974822 11974822 CTCCTTCGTCGATCCCTAATTGGCCAGGCCTGACCCTCTTGGACCTTTCTTCTTTGCCGACAACC CTCCTTCGTCGATCCCTAATTGGCCAGGCCTGGCCCTCTTGGACCTTTCTTCTTTGCCGACAACC A G PLOD1 Ensembl:ENSG00000083444 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:11974776..11974850 26863196 MeRIP-seq:(Medium) rs201169472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_323581,Human_RBP_ID_801246,Human_RBP_ID_3986976,Human_RBP_ID_5108987,Human_RBP_ID_8282984,Human_RBP_ID_17646869,Human_RBP_ID_18186847,Human_RBP_ID_22426909,Human_RBP_ID_27166245,Human_RBP_ID_27386817 RMVar_hsa_circ_129220,RMVar_hsa_circ_87402,RMVar_hsa_circ_86782,RMVar_hsa_circ_129221,RMVar_hsa_circ_116125,RMVar_hsa_circ_129225,RMVar_hsa_circ_115355,RMVar_hsa_circ_129232,RMVar_hsa_circ_120563,RMVar_hsa_circ_96850,RMVar_hsa_circ_129234,RMVar_hsa_circ_100758,RMVar_hsa_circ_129235,RMVar_hsa_circ_99318,RMVar_hsa_circ_129238,RMVar_hsa_circ_129239 67452 RMVar_ID_67452 Human_SNP_ID_3283280 m1A Human chr1 - 11980480 11980480 11980480 CGCCACCCCGGCTTGCTCGCCCTCTCACCTTCACCTTCCCGGCCTCGCGGCGGCCATCACACTCA CGCCACCCCGGCTTGCTCGCCCTCTCACCTTCGCCTTCCCGGCCTCGCGGCGGCCATCACACTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:11980470..11980549;chr1:11980217..11980767 26863196 MeRIP-seq:(Medium) rs902164898 Functional Loss SNV dbSNP153 33..33 33 - - - 67453 RMVar_ID_67453 Human_SNP_ID_3284161 m1A Human chr1 - 11983779 11983779 11983779 CACCCGCTCCATGAAGCCTCCTCTGATGCCTCATAGAGAACAAACAACATCACAGACTTCTGGTT CACCCGCTCCATGAAGCCTCCTCTGATGCCTCTTAGAGAACAAACAACATCACAGACTTCTGGTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11983774..11983964 26863196 MeRIP-seq:(Medium) rs956831517 Functional Loss SNV dbSNP153 33..33 33 - - - 67454 RMVar_ID_67454 Human_SNP_ID_3284172 m1A Human chr1 - 11983826 11983826 11983826 ACCCATTTGGCATACTCCTACTGTCCTTCTAGACCCAACTCAAGTGTCACCCGCTCCATGAAGCC ACCCATTTGGCATACTCCTACTGTCCTTCTAGCCCCAACTCAAGTGTCACCCGCTCCATGAAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:11983819..11984001 26863196 MeRIP-seq:(Medium) rs910471810 Functional Loss SNV dbSNP153 33..33 33 - - - 67455 RMVar_ID_67455 Human_SNP_ID_3291909 m1A Human chr1 + 12011576 12011576 12011576 GTACCTGCAGCCCAGCAGATAGTGGGCACCTGAGGCGGAGTCTGCGTGGAGAGGGGCGGTGCTGC GTACCTGCAGCCCAGCAGATAGTGGGCACCTGGGGCGGAGTCTGCGTGGAGAGGGGCGGTGCTGC A G MFN2 Ensembl:ENSG00000116688 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:12011526..12011750 32194978 MeRIP-seq:(Medium) rs773112358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5899816,Human_RBP_ID_8733904,Human_RBP_ID_17723567,Human_RBP_ID_22779410 Human_Splice_Rec_18522,Human_Splice_Rec_18572 RMVar_hsa_circ_129260,RMVar_hsa_circ_111502,RMVar_hsa_circ_103957,RMVar_hsa_circ_129262,RMVar_hsa_circ_129267,RMVar_hsa_circ_113978 67456 RMVar_ID_67456 Human_SNP_ID_3291948 m1A Human chr1 + 12011686 12011686 12011686 CTGCCCCCTGGCCACTGCCAAGAGAATGAAGCACCCAGTCTCGTACCATTTTGAGCCCTCCAGCA CTGCCCCCTGGCCACTGCCAAGAGAATGAAGCGCCCAGTCTCGTACCATTTTGAGCCCTCCAGCA A G MFN2 Ensembl:ENSG00000116688 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:12011617..12011800 26863196 MeRIP-seq:(Medium) rs886045222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27386963 Human_miRNA_ID_2245981,Human_miRNA_ID_2850287,Human_miRNA_ID_3085006 Clinvar_Rec_272 RMVar_hsa_circ_129260,RMVar_hsa_circ_111502,RMVar_hsa_circ_103957,RMVar_hsa_circ_129262,RMVar_hsa_circ_129267,RMVar_hsa_circ_113978 67457 RMVar_ID_67457 Human_SNP_ID_3294233 m1A Human chr1 - 12019534 12019534 12019534 CGCCCAGCACTCACCCGGCAGAATCCCCTAGCATGCGCCGCCGTAGCAGCCGCAGCCGCCTGAGC CGCCCAGCACTCACCCGGCAGAATCCCCTAGCCTGCGCCGCCGTAGCAGCCGCAGCCGCCTGAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:12019476..12019613 26863196 MeRIP-seq:(Medium) rs921164498 Functional Loss SNV dbSNP153 33..33 33 - - - 67458 RMVar_ID_67458 Human_SNP_ID_3294870 m1A Human chr1 + 12021693 12021693 12021693 TGGAACCCAGCCCTGAGGACATCCTGCGGCCCAGGGGCAAGTGACACCTGCTGAGAGAGGCCCAG TGGAACCCAGCCCTGAGGACATCCTGCGGCCCGGGGGCAAGTGACACCTGCTGAGAGAGGCCCAG A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:12021626..12021825 26863196 MeRIP-seq:(Medium) rs1314926930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073564,Human_RBP_ID_17723590,Human_RBP_ID_18967210,Human_RBP_ID_23204944 Human_Splice_Rec_18590 RMVar_hsa_circ_25416,RMVar_hsa_circ_325806,RMVar_hsa_circ_377014 67459 RMVar_ID_67459 Human_SNP_ID_3295101 m1A Human chr1 - 12022262 12022262 12022262 GACTCCTGGTGCTGGCATTTGGCAGGTGGGAGAGAGGCCACCCCCGATCTGGCCACATCACGGAG GACTCCTGGTGCTGGCATTTGGCAGGTGGGAGGGAGGCCACCCCCGATCTGGCCACATCACGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12022211..12022379 26863196 MeRIP-seq:(Medium) rs745592384 Functional Loss SNV dbSNP153 33..33 33 - - - 67460 RMVar_ID_67460 Human_SNP_ID_3297126 m1A Human chr1 - 12029283 12029283 12029283 CTACTCAGCGGCCTAGCCGAGGGCCCGCACTCACATTCATGGTCTTCCTCCACGCCGCTGCCACT CTACTCAGCGGCCTAGCCGAGGGCCCGCACTCTCATTCATGGTCTTCCTCCACGCCGCTGCCACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12029226..12029428 26863196 MeRIP-seq:(Medium) rs954726916 Functional Loss SNV dbSNP153 33..33 33 - - - 67461 RMVar_ID_67461 Human_SNP_ID_3297956 m1A Human chr1 - 12031688 12031688 12031688 TGGATGGGGAATAGGGAAGTCTCAGGGGGGCCACTTGAAAGGGACAGGTCATCCCCAGTTCCAGC TGGATGGGGAATAGGGAAGTCTCAGGGGGGCCGCTTGAAAGGGACAGGTCATCCCCAGTTCCAGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:12031687..12031842 26863410 MeRIP-seq:(Medium) rs753831122 Functional Loss SNV dbSNP153 33..33 33 - - - 67462 RMVar_ID_67462 Human_SNP_ID_3298015 m1A Human chr1 + 12031798 12031798 12031798 GCCCCAGGTCCCTCGGCCCCACGTCCCACGGCAGAAGCCCTGAGGACTGACTCCTGGGGGAGAAC GCCCCAGGTCCCTCGGCCCCACGTCCCACGGCCGAAGCCCTGAGGACTGACTCCTGGGGGAGAAC A C MIIP Ensembl:ENSG00000116691 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:12031747..12031946 32194978 MeRIP-seq:(Medium) rs1376309568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5136077,Human_RBP_ID_21879691 Human_Splice_Rec_18606,Human_Splice_Rec_18616,Human_Splice_Rec_18626,Human_Splice_Rec_18640 RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 67463 RMVar_ID_67463 Human_SNP_ID_3298023 m1A Human chr1 - 12031817 12031817 12031817 TGGAGGCGGCGGGAATGCTGTTCTCCCCCAGGAGTCAGTCCTCAGGGCTTCTGCCGTGGGACGTG TGGAGGCGGCGGGAATGCTGTTCTCCCCCAGGTGTCAGTCCTCAGGGCTTCTGCCGTGGGACGTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12031768..12031843 26863196 MeRIP-seq:(Medium) rs758464348 Functional Loss SNV dbSNP153 33..33 33 - - - 67464 RMVar_ID_67464 Human_SNP_ID_3298024 m1A Human chr1 - 12031817 12031817 12031817 TGGAGGCGGCGGGAATGCTGTTCTCCCCCAGGAGTCAGTCCTCAGGGCTTCTGCCGTGGGACGTG TGGAGGCGGCGGGAATGCTGTTCTCCCCCAGGGGTCAGTCCTCAGGGCTTCTGCCGTGGGACGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12031768..12031843 26863196 MeRIP-seq:(Medium) rs758464348 Functional Loss SNV dbSNP153 33..33 33 - - - 67465 RMVar_ID_67465 Human_SNP_ID_3360820 m1A Human chr1 - 12275903 12275902 12275903 ACTCGGGAGGTGGGGTGTTAGGAGGTGTGGCCAGGGGGGTCTTATATTCATCATCACTAAACTGG ACTCGGGAGGTGGGGTGTTAGGAGGTGTGGCC_GGGGGGTCTTATATTCATCATCACTAAACTGG CT C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:12275855..12275939 26863410 MeRIP-seq:(Medium) rs1263796874 Functional Loss DEL dbSNP153 33..33 33 - - - 67466 RMVar_ID_67466 Human_SNP_ID_3432015 m1A Human chr1 - 12568159 12568159 12568159 AGTCCCAGGACCTTTGCACAGGACTGATGGGTATAACTGACCCCCACAGGGAGGCAGGAAAACAG AGTCCCAGGACCTTTGCACAGGACTGATGGGTGTAACTGACCCCCACAGGGAGGCAGGAAAACAG T C DHRS3 Ensembl:ENSG00000162496 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:12568108..12568358 32194978 MeRIP-seq:(Medium) rs4580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1410041,Human_RBP_ID_3988478,Human_RBP_ID_18157477,Human_RBP_ID_22022761,Human_RBP_ID_27554291 Human_miRNA_ID_2244806 GWAS_ID_8029,GWAS_ID_8030,GWAS_ID_8031,GWAS_ID_8032,GWAS_ID_8033 RMVar_hsa_circ_98104,RMVar_hsa_circ_129345 67467 RMVar_ID_67467 Human_SNP_ID_3434786 m1A Human chr1 - 12578958 12578958 12578958 AGCTGCTCCACCCTGACACCCCATCTGCCCTCAGACCACCAAGGCCTTCCTGCCGCGTATGCTGG AGCTGCTCCACCCTGACACCCCATCTGCCCTCGGACCACCAAGGCCTTCCTGCCGCGTATGCTGG T C DHRS3,MIR6730 Ensembl:ENSG00000162496,Ensembl:ENSG00000276830 Protein coding,miRNA intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:12578922..12579813 32194978 MeRIP-seq:(Medium) rs111644113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849461,Human_RBP_ID_22632879 RMVar_hsa_circ_358191,RMVar_hsa_circ_322736,RMVar_hsa_circ_129347,RMVar_hsa_circ_278948,RMVar_hsa_circ_301191,RMVar_hsa_circ_129348 67468 RMVar_ID_67468 Human_SNP_ID_3435323 m1A Human chr1 - 12580600 12580600 12580600 AGGAGACGACGGAGGAGATCCGGCAGATGGGCACTGAGTGCCATTACTTCATCTGTGATGTGGGC AGGAGACGACGGAGGAGATCCGGCAGATGGGCGCTGAGTGCCATTACTTCATCTGTGATGTGGGC T C DHRS3 Ensembl:ENSG00000162496 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:12580551..12580703;chr1:12580551..12580701 26863196 MeRIP-seq:(Medium) rs777938819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22748868 Human_Splice_Rec_19460,Human_Splice_Rec_19461,Human_Splice_Rec_19470,Human_Splice_Rec_19471,Human_Splice_Rec_19476,Human_Splice_Rec_19477,Human_Splice_Rec_19482 Human_miRNA_ID_2133281 RMVar_hsa_circ_358191,RMVar_hsa_circ_129347,RMVar_hsa_circ_301191,RMVar_hsa_circ_54634 67469 RMVar_ID_67469 Human_SNP_ID_3435844 m1A Human chr1 + 12582788 12582784 12582788 GTCCATCCGTCCACTCTCCCGTTCACCAGTCCATCCATCTATCCACCACACTTCATCCATCCATC GTCCATCCGTCCACTCTCCCGTTCACCAG____TCCATCTATCCACCACACTTCATCCATCCATC GTCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:12582630..12583360 26863196 MeRIP-seq:(Medium) rs1449192569 Functional Loss DEL dbSNP153 30..33 33 - - - 67470 RMVar_ID_67470 Human_SNP_ID_3436213 m1A Human chr1 + 12583651 12583651 12583651 ATCCATCCATCCATCCCTCCCTCACATACCCCACTCCATCCATCCATCCATTCATCTGTCCATCC ATCCATCCATCCATCCCTCCCTCACATACCCCCCTCCATCCATCCATCCATTCATCTGTCCATCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:12583647..12583924 26863196 MeRIP-seq:(Medium) rs1222990762 Functional Loss SNV dbSNP153 33..33 33 - - - 67471 RMVar_ID_67471 Human_SNP_ID_3436796 m1A Human chr1 - 12585250 12585250 12585250 ACACAGACACAGAGAGACACACACTCAGAGACACAGAGACACACACTCACATAGACACACACACA ACACAGACACAGAGAGACACACACTCAGAGACTCAGAGACACACACTCACATAGACACACACACA T A DHRS3 Ensembl:ENSG00000162496 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:12585247..12585407 26863196 MeRIP-seq:(Medium) rs936177717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190120,Human_RBP_ID_2090802,Human_RBP_ID_9410435 67472 RMVar_ID_67472 Human_SNP_ID_3437120 m1A Human chr1 + 12586385 12586385 12586385 TGAGCTTTGAGGGTTCCACTCTCCTCACATGCAACCCCACGCCCCGCGTTCATCCCCACCCAGCC TGAGCTTTGAGGGTTCCACTCTCCTCACATGCGACCCCACGCCCCGCGTTCATCCCCACCCAGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12586382..12586464 26863196 MeRIP-seq:(Medium) rs961584077 Functional Loss SNV dbSNP153 33..33 33 - - - 67473 RMVar_ID_67473 Human_SNP_ID_3438734 m1A Human chr1 - 12592888 12592888 12592888 GTCAGGCTGACAGGGTGCGTGGTGGAGTGGGCATACAGTGAGAGAAAACACTTAATGTGGGACAG GTCAGGCTGACAGGGTGCGTGGTGGAGTGGGCGTACAGTGAGAGAAAACACTTAATGTGGGACAG T C DHRS3 Ensembl:ENSG00000162496 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:12592886..12593005 26863196 MeRIP-seq:(Medium) rs1048547734 Functional Loss SNV dbSNP153 33..33 33 - - - 67474 RMVar_ID_67474 Human_SNP_ID_3438735 m1A Human chr1 - 12592888 12592888 12592888 GTCAGGCTGACAGGGTGCGTGGTGGAGTGGGCATACAGTGAGAGAAAACACTTAATGTGGGACAG GTCAGGCTGACAGGGTGCGTGGTGGAGTGGGCCTACAGTGAGAGAAAACACTTAATGTGGGACAG T G DHRS3 Ensembl:ENSG00000162496 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:12592886..12593005 26863196 MeRIP-seq:(Medium) rs1048547734 Functional Loss SNV dbSNP153 33..33 33 - - - 67475 RMVar_ID_67475 Human_SNP_ID_3444370 m1A Human chr1 - 12616577 12616577 12616577 CCGACACTGAGAGGCCCAGGTGTTTGGAAAGCAGGAAAGAGGAGGCCAGGGTAAGCAGCTACTGA CCGACACTGAGAGGCCCAGGTGTTTGGAAAGCGGGAAAGAGGAGGCCAGGGTAAGCAGCTACTGA T C DHRS3 Ensembl:ENSG00000162496 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:12616574..12616690 26863196 MeRIP-seq:(Medium) rs1471541697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10554155 Human_Splice_Rec_19469,Human_Splice_Rec_19481 67476 RMVar_ID_67476 Human_SNP_ID_3729034 m1A Human chr1 + 13749461 13749461 13749461 GATTGAGGAAGAGCGAGCCAGCGCCCGGAGCAAGCGGAGCTCCCCCAAGAGCCGGAAAGGTAGGA GATTGAGGAAGAGCGAGCCAGCGCCCGGAGCAGGCGGAGCTCCCCCAAGAGCCGGAAAGGTAGGA A G PRDM2 Ensembl:ENSG00000116731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:13749414..13749531 26863196 MeRIP-seq:(Medium) rs553659427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221447,Human_RBP_ID_26310241 Human_Splice_Rec_19845,Human_Splice_Rec_19859,Human_Splice_Rec_19875,Human_Splice_Rec_19887,Human_Splice_Rec_19897,Human_Splice_Rec_19903,Human_Splice_Rec_19907,Human_Splice_Rec_19913,Human_Splice_Rec_19921,Human_Splice_Rec_19923,Human_Splice_Rec_19931,Human_Splice_Rec_19937 RMVar_hsa_circ_301894,RMVar_hsa_circ_367491,RMVar_hsa_circ_129356,RMVar_hsa_circ_278680,RMVar_hsa_circ_129355,RMVar_hsa_circ_35349,RMVar_hsa_circ_280626,RMVar_hsa_circ_284522,RMVar_hsa_circ_129358,RMVar_hsa_circ_129359,RMVar_hsa_circ_295913,RMVar_hsa_circ_329511,RMVar_hsa_circ_45588 67477 RMVar_ID_67477 Human_SNP_ID_3729051 m1A Human chr1 + 13749476 13749476 13749476 AGCCAGCGCCCGGAGCAAGCGGAGCTCCCCCAAGAGCCGGAAAGGTAGGAGCCCCCCGGCCCGCC AGCCAGCGCCCGGAGCAAGCGGAGCTCCCCCAGGAGCCGGAAAGGTAGGAGCCCCCCGGCCCGCC A G PRDM2 Ensembl:ENSG00000116731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:13749427..13749543 26863196 MeRIP-seq:(Medium) rs1211006367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26310241 Human_Splice_Rec_19845,Human_Splice_Rec_19859,Human_Splice_Rec_19875,Human_Splice_Rec_19887,Human_Splice_Rec_19897,Human_Splice_Rec_19903,Human_Splice_Rec_19907,Human_Splice_Rec_19913,Human_Splice_Rec_19921,Human_Splice_Rec_19923,Human_Splice_Rec_19931,Human_Splice_Rec_19937 RMVar_hsa_circ_301894,RMVar_hsa_circ_367491,RMVar_hsa_circ_129356,RMVar_hsa_circ_278680,RMVar_hsa_circ_129355,RMVar_hsa_circ_35349,RMVar_hsa_circ_280626,RMVar_hsa_circ_284522,RMVar_hsa_circ_129358,RMVar_hsa_circ_129359,RMVar_hsa_circ_295913,RMVar_hsa_circ_329511,RMVar_hsa_circ_45588 67478 RMVar_ID_67478 Human_SNP_ID_3736658 m1A Human chr1 - 13778591 13778591 13778591 CTCCTCCTCTTCCTCCTCCTCCTCTTCCCCCAAATCATTCACCTCACAAGCTGCCGCTTCTAATC CTCCTCCTCTTCCTCCTCCTCCTCTTCCCCCATATCATTCACCTCACAAGCTGCCGCTTCTAATC T A lnc-LRRC38-2 RNACentral:URS00008C1D5A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:13778362..13778664 26863196 MeRIP-seq:(Medium) rs752401389 Functional Loss SNV dbSNP153 33..33 33 - - - 67479 RMVar_ID_67479 Human_SNP_ID_3736659 m1A Human chr1 - 13778591 13778591 13778591 CTCCTCCTCTTCCTCCTCCTCCTCTTCCCCCAAATCATTCACCTCACAAGCTGCCGCTTCTAATC CTCCTCCTCTTCCTCCTCCTCCTCTTCCCCCAGATCATTCACCTCACAAGCTGCCGCTTCTAATC T C lnc-LRRC38-2 RNACentral:URS00008C1D5A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:13778362..13778664 26863196 MeRIP-seq:(Medium) rs752401389 Functional Loss SNV dbSNP153 33..33 33 - - - 67480 RMVar_ID_67480 Human_SNP_ID_3737573 m1A Human chr1 + 13780832 13780832 13780832 CATCTCCACACCCATGCCCCTCTCCACTCTCAAATGCCACCGCACAGTCCCCACTTCCAATTCTG CATCTCCACACCCATGCCCCTCTCCACTCTCAGATGCCACCGCACAGTCCCCACTTCCAATTCTG A G PRDM2 Ensembl:ENSG00000116731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:13780679..13780996 26863196 MeRIP-seq:(Medium) rs745791226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2091026,Human_RBP_ID_5125165,Human_RBP_ID_17071028,Human_RBP_ID_17557622,Human_RBP_ID_18927958 Human_miRNA_ID_2076830 RMVar_hsa_circ_367491,RMVar_hsa_circ_129363,RMVar_hsa_circ_51101,RMVar_hsa_circ_347248,RMVar_hsa_circ_311066,RMVar_hsa_circ_129362,RMVar_hsa_circ_296927 67481 RMVar_ID_67481 Human_SNP_ID_3737617 m1A Human chr1 - 13780905 13780905 13780905 GCCCGGGTGAGGCGGCAGACATCAGGGGCTCCACGGGAGGAATGGGAGAGGGAGAGGGGGACACT GCCCGGGTGAGGCGGCAGACATCAGGGGCTCCGCGGGAGGAATGGGAGAGGGAGAGGGGGACACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:13780719..13780951 26863196 MeRIP-seq:(Medium) rs747751413 Functional Loss SNV dbSNP153 33..33 33 - - - 67482 RMVar_ID_67482 Human_SNP_ID_681091545 m1A Human chr20 - 40687458 40687458 40687458 GCTGCCCGGAGAGTAGTCCGCGCCAGGAAGAGAGCAACGAGGAAAGGAGAGGGACTCTGGCGTCC GCTGCCCGGAGAGTAGTCCGCGCCAGGAAGAGGGCAACGAGGAAAGGAGAGGGACTCTGGCGTCC T C MAFB Ensembl:ENSG00000204103 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:40687407..40687492 26863196 MeRIP-seq:(Medium) rs1400787380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4647651 67483 RMVar_ID_67483 Human_SNP_ID_681176692 m1A Human chr20 - 41028883 41028883 41028883 TGAGGCTGCTACCACGGCGGCGACGCTGCCTGACTGCCGGGCGGGCGGCGAGAACAGACCCCAGC TGAGGCTGCTACCACGGCGGCGACGCTGCCTGCCTGCCGGGCGGGCGGCGAGAACAGACCCCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:41028826..41029125;chr20:41028826..41077650 26863196 MeRIP-seq:(Medium) rs1386630423 Functional Loss SNV dbSNP153 33..33 33 - - - 67484 RMVar_ID_67484 Human_SNP_ID_681176713 m1A Human chr20 + 41028945 41028945 41028945 TCAGCCGTTTCTGGAGTCTCGGGCCCACAGTCACCGCCGCTTACCTGCGCCTCCTCGAGCCTCCG TCAGCCGTTTCTGGAGTCTCGGGCCCACAGTCCCCGCCGCTTACCTGCGCCTCCTCGAGCCTCCG A C TOP1 Ensembl:ENSG00000198900 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:41028867..41028950 26863410 MeRIP-seq:(Medium) rs1403091659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4647683,Human_RBP_ID_5423741,Human_RBP_ID_5445925,Human_RBP_ID_5503369,Human_RBP_ID_9390627,Human_RBP_ID_22533644,Human_RBP_ID_26820861,Human_RBP_ID_27021170 67485 RMVar_ID_67485 Human_SNP_ID_681176716 m1A Human chr20 - 41028954 41028954 41028954 CGGGGACTCCGGAGGCTCGAGGAGGCGCAGGTAAGCGGCGGTGACTGTGGGCCCGAGACTCCAGA CGGGGACTCCGGAGGCTCGAGGAGGCGCAGGTGAGCGGCGGTGACTGTGGGCCCGAGACTCCAGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:41028826..41029125 26863410 MeRIP-seq:(Medium) rs891857081 Functional Loss SNV dbSNP153 33..33 33 - - - 67486 RMVar_ID_67486 Human_SNP_ID_681188860 m1A Human chr20 + 41081237 41081237 41081237 AAGAAGGAGAAGAAAAGAAAACTAGAAGAAGAAGAGGTTAGTAAAGAGACTTAGGTCCTTTGGGG AAGAAGGAGAAGAAAAGAAAACTAGAAGAAGAGGAGGTTAGTAAAGAGACTTAGGTCCTTTGGGG A G TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:41081218..41081293 26863196 MeRIP-seq:(Medium) rs151248842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924006,Human_RBP_ID_1601123,Human_RBP_ID_1929851,Human_RBP_ID_9348034,Human_RBP_ID_24546663 Human_Splice_Rec_2083682,Human_Splice_Rec_2083683 RMVar_hsa_circ_58260,RMVar_hsa_circ_353056,RMVar_hsa_circ_357648,RMVar_hsa_circ_339116,RMVar_hsa_circ_210159,RMVar_hsa_circ_210160,RMVar_hsa_circ_58635,RMVar_hsa_circ_350180,RMVar_hsa_circ_350360,RMVar_hsa_circ_62152,RMVar_hsa_circ_356975,RMVar_hsa_circ_73675,RMVar_hsa_circ_63755 67487 RMVar_ID_67487 Human_SNP_ID_681189568 m1A Human chr20 + 41084475 41084475 41084475 TCACCATGTTTCTTTGTAGGATGGTAAATTGAAAAAACCCAAGAATAAAGATAAAGATAAAAAAG TCACCATGTTTCTTTGTAGGATGGTAAATTGAGAAAACCCAAGAATAAAGATAAAGATAAAAAAG A G TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41081117..41084575 26863196 MeRIP-seq:(Medium) rs1362082972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63724,Human_RBP_ID_1601124,Human_RBP_ID_2685287,Human_RBP_ID_3960800,Human_RBP_ID_14108864,Human_RBP_ID_23002258,Human_RBP_ID_24546664,Human_RBP_ID_25612375 Human_Splice_Rec_2083684,Human_Splice_Rec_2083685 RMVar_hsa_circ_58260,RMVar_hsa_circ_353056,RMVar_hsa_circ_357648,RMVar_hsa_circ_210160,RMVar_hsa_circ_58635,RMVar_hsa_circ_350360,RMVar_hsa_circ_62152,RMVar_hsa_circ_210162,RMVar_hsa_circ_20098,RMVar_hsa_circ_63755,RMVar_hsa_circ_78804,RMVar_hsa_circ_210163 67488 RMVar_ID_67488 Human_SNP_ID_681202114 m1A Human chr20 + 41137670 41137670 41137670 AGCCATGGCGGGCGCCGCGTCCCCTTGCGCCAACGGCTGCGGGCCCGGCGCGCCCTCGGACGCCG AGCCATGGCGGGCGCCGCGTCCCCTTGCGCCAGCGGCTGCGGGCCCGGCGCGCCCTCGGACGCCG A G PLCG1 Ensembl:ENSG00000124181 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:41137626..41137725 26863196 MeRIP-seq:(Medium) rs1029753571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659845,Human_RBP_ID_8857394,Human_RBP_ID_18423120,Human_RBP_ID_18471118,Human_RBP_ID_22601232 RMVar_hsa_circ_86238,RMVar_hsa_circ_210171 67489 RMVar_ID_67489 Human_SNP_ID_681204890 m1A Human chr20 - 41149444 41149444 41149444 CCCCCTGGGTCAGCTAAGAGCATCACCATTCAAACAGGTACCCAAACTCCAAACTTCAGAATGAT CCCCCTGGGTCAGCTAAGAGCATCACCATTCAGACAGGTACCCAAACTCCAAACTTCAGAATGAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41149441..41149766 26863196 MeRIP-seq:(Medium) rs75144367 Functional Loss SNV dbSNP153 33..33 33 - - - 67490 RMVar_ID_67490 Human_SNP_ID_681209992 m1A Human chr20 + 41168852 41168852 41168852 CTTCATCAAGAGCGCCATCATCCAGAATGTGGAGAAGCAAGAGGGAGGCTGGTAAGCCAGTGGTG CTTCATCAAGAGCGCCATCATCCAGAATGTGGCGAAGCAAGAGGGAGGCTGGTAAGCCAGTGGTG A C PLCG1 Ensembl:ENSG00000124181 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:41168801..41168883 26863196 MeRIP-seq:(Medium) rs1568753476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960243,Human_RBP_ID_9389269,Human_RBP_ID_19005767,Human_RBP_ID_26342983 Human_Splice_Rec_2083800,Human_Splice_Rec_2083801,Human_Splice_Rec_2083862,Human_Splice_Rec_2083863,Human_Splice_Rec_2083920,Human_Splice_Rec_2083921,Human_Splice_Rec_2083926,Human_Splice_Rec_2083927,Human_Splice_Rec_2083934,Human_Splice_Rec_2083935,Human_Splice_Rec_2083941,Human_Splice_Rec_2083947 RMVar_hsa_circ_56952,RMVar_hsa_circ_52456,RMVar_hsa_circ_116497,RMVar_hsa_circ_210181,RMVar_hsa_circ_85401,RMVar_hsa_circ_210180,RMVar_hsa_circ_210184,RMVar_hsa_circ_99755,RMVar_hsa_circ_210183 67491 RMVar_ID_67491 Human_SNP_ID_681210588 m1A Human chr20 - 41170558 41170558 41170558 TATGCCTCAGCCCCCACTCCACTCCTGCTTCCAGCCCAGGACTTCTCCTCTTACCTCTGGTCTTG TATGCCTCAGCCCCCACTCCACTCCTGCTTCCGGCCCAGGACTTCTCCTCTTACCTCTGGTCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41170540..41170665 26863196 MeRIP-seq:(Medium) rs1339665503 Functional Loss SNV dbSNP153 33..33 33 - - - 67492 RMVar_ID_67492 Human_SNP_ID_681211469 m1A Human chr20 - 41173482 41173482 41173482 TTGGTGCTGTCATACTCAGCTCCAGCCACCTCAATCTCCACAAAAGGACACACAATGCCTCGGCC TTGGTGCTGTCATACTCAGCTCCAGCCACCTCGATCTCCACAAAAGGACACACAATGCCTCGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:41172757..41173500 32194978 MeRIP-seq:(Medium) rs1399666715 Functional Loss SNV dbSNP153 33..33 33 - - - 67493 RMVar_ID_67493 Human_SNP_ID_681211954 m1A Human chr20 - 41174791 41174791 41174791 CCAAGGGGCTTCGGCCATGGTCCTGGCCCCACAAGATGGAAGGATCCATCTCCAGAAGTCAGGGC CCAAGGGGCTTCGGCCATGGTCCTGGCCCCACTAGATGGAAGGATCCATCTCCAGAAGTCAGGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:41174741..41175092 32194978 MeRIP-seq:(Medium) rs945039140 Functional Loss SNV dbSNP153 33..33 33 - - - 67494 RMVar_ID_67494 Human_SNP_ID_681212104 m1A Human chr20 - 41175350 41175349 41175350 ATACTGAGTCTTCTTTGACTTAAAAACAAAAAACCTCACCAAAATAGGCTCTGCTATTTCTTCTC ATACTGAGTCTTCTTTGACTTAAAAACAAAAA_CCTCACCAAAATAGGCTCTGCTATTTCTTCTC GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:41174960..41175537 26863196 MeRIP-seq:(Medium) rs982242541 Functional Loss DEL dbSNP153 33..33 33 - - - 67495 RMVar_ID_67495 Human_SNP_ID_681212124 m1A Human chr20 + 41175402 41175402 41175402 GAAGACTCAGTATGCTTTCCCTGAGGAATGAAAAAGGGATTGAGGAGTTGCCTGACTCCTGGGTG GAAGACTCAGTATGCTTTCCCTGAGGAATGAAGAAGGGATTGAGGAGTTGCCTGACTCCTGGGTG A G PLCG1 Ensembl:ENSG00000124181 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:41175351..41175565 26863196 MeRIP-seq:(Medium) rs890298050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119175,Human_RBP_ID_5147915,Human_RBP_ID_5529445,Human_RBP_ID_8204569,Human_RBP_ID_17659368,Human_RBP_ID_18167687,Human_RBP_ID_23212308,Human_RBP_ID_23905534,Human_RBP_ID_26493096 Human_miRNA_ID_544786,Human_miRNA_ID_580022,Human_miRNA_ID_2142678,Human_miRNA_ID_2193822,Human_miRNA_ID_2208030,Human_miRNA_ID_3046487 RMVar_hsa_circ_99755,RMVar_hsa_circ_210183,RMVar_hsa_circ_77450,RMVar_hsa_circ_210186 67496 RMVar_ID_67496 Human_SNP_ID_681219311 m1A Human chr20 + 41202877 41202877 41202877 CCCTCATCCTCAGCAGCCTCCTCTTCCTCCTGAGAGGCATTCTCCTCAGCCTTCTTGGTCTCCTC CCCTCATCCTCAGCAGCCTCCTCTTCCTCCTGGGAGGCATTCTCCTCAGCCTTCTTGGTCTCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:41202827..41202969 26863196 MeRIP-seq:(Medium) rs746116379 Functional Loss SNV dbSNP153 33..33 33 - - - 67497 RMVar_ID_67497 Human_SNP_ID_681243118 m1A Human chr20 + 41303664 41303664 41303664 CAGGCACTCCTCCTCTGGCAATGCTACTGGCCATCTCCTGTGCATGCCCCTCCATCCACAGAAGA CAGGCACTCCTCCTCTGGCAATGCTACTGGCCGTCTCCTGTGCATGCCCCTCCATCCACAGAAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:41303662..41303809 26863196 MeRIP-seq:(Medium) rs972670532 Functional Loss SNV dbSNP153 33..33 33 - - - 67498 RMVar_ID_67498 Human_SNP_ID_681246487 m1A Human chr20 - 41317560 41317540 41317561 CCGCCCGCCCGGCCGCGGGGAGGGAGGCCCGCAGCGCGGGAAGAGCGGCCCGGTCGCGGGCGCCG CCGCCCGCCCGGCCGCGGGGAGGGAGGCCCG_____________________GTCGCGGGCGCCG CCGGGCCGCTCTTCCCGCGCTG C ZHX3 Ensembl:ENSG00000174306 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41317454..41317641 26863196 MeRIP-seq:(Medium) rs1261779757 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_831438,Human_RBP_ID_4648006 Human_Splice_Rec_2084067,Human_Splice_Rec_2084107,Human_Splice_Rec_2084159 RMVar_hsa_circ_108985,RMVar_hsa_circ_210189 67499 RMVar_ID_67499 Human_SNP_ID_681252610 m1A Human chr20 + 41340931 41340931 41340931 AAGCGCCAAGTGACTGAGGGCCGAAGACACTCACCTGTGGAGCCTGTGCACGTAGGTAGAGGCGG AAGCGCCAAGTGACTGAGGGCCGAAGACACTCGCCTGTGGAGCCTGTGCACGTAGGTAGAGGCGG A G LPIN3 Ensembl:ENSG00000132793 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:41340808..41341000 26863196 MeRIP-seq:(Medium) rs1450633261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2084161,Human_Splice_Rec_2084199 RMVar_hsa_circ_79614,RMVar_hsa_circ_210195 67500 RMVar_ID_67500 Human_SNP_ID_681253677 m1A Human chr20 + 41345843 41345843 41345843 ACGTGGGGCAGCTGGCGGAGACGGTGTTTGGGACGGTGAAGGAGCTGTACCGGGGCCTGAACCCA ACGTGGGGCAGCTGGCGGAGACGGTGTTTGGGCCGGTGAAGGAGCTGTACCGGGGCCTGAACCCA A C LPIN3 Ensembl:ENSG00000132793 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:41345769..41345882 26863196 MeRIP-seq:(Medium) rs1287233397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8234996,Human_RBP_ID_19004275 Human_Splice_Rec_2084162,Human_Splice_Rec_2084200 RMVar_hsa_circ_79614,RMVar_hsa_circ_210196,RMVar_hsa_circ_210195,RMVar_hsa_circ_367002 67501 RMVar_ID_67501 Human_SNP_ID_681269213 m1A Human chr20 - 41404712 41404712 41404712 ACTCCCACCCAGAGCCTGCTCCCAGCTGTGAAAGGGAGCCCAGCGGTGATGAGAACTGTGCCGAA ACTCCCACCCAGAGCCTGCTCCCAGCTGTGAAGGGGAGCCCAGCGGTGATGAGAACTGTGCCGAA T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41404661..41404749 26863196 MeRIP-seq:(Medium) rs1262581758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564271,Human_RBP_ID_5529123,Human_RBP_ID_24553459,Human_RBP_ID_27485937 67502 RMVar_ID_67502 Human_SNP_ID_681271430 m1A Human chr20 + 41413748 41413748 41413748 TTCACCTGAGCACTCCTCTCCCGCTCTTGTCCACTTGGTACACTTTAACTCCATCCTGACTGCCG TTCACCTGAGCACTCCTCTCCCGCTCTTGTCCGCTTGGTACACTTTAACTCCATCCTGACTGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41413746..41413893 26863196 MeRIP-seq:(Medium) rs778256785 Functional Loss SNV dbSNP153 33..33 33 - - - 67503 RMVar_ID_67503 Human_SNP_ID_681272169 m1A Human chr20 + 41416700 41416700 41416700 AACCAGCACTGCTGGTTAATACCGGGGTGGGCAGTGTGCCTGAGGGCTCATACTGCTGGCTAGAG AACCAGCACTGCTGGTTAATACCGGGGTGGGCCGTGTGCCTGAGGGCTCATACTGCTGGCTAGAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41416623..41417276 32194978 MeRIP-seq:(Medium) rs1434555061 Functional Loss SNV dbSNP153 33..33 33 - - - 67504 RMVar_ID_67504 Human_SNP_ID_681279265 m1A Human chr20 - 41445670 41445670 41445670 AGCCGATAAGTCACTTCTCATTGGCGTGTTCAAGCATGGTGTGTATTTCTCTGAAGGCGTTCCCT AGCCGATAAGTCACTTCTCATTGGCGTGTTCAGGCATGGTGTGTATTTCTCTGAAGGCGTTCCCT T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41437325..41445675 32194978 MeRIP-seq:(Medium) rs752641036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960255,Human_RBP_ID_19004295 Human_Splice_Rec_2084320,Human_Splice_Rec_2084321,Human_Splice_Rec_2084368,Human_Splice_Rec_2084369,Human_Splice_Rec_2084394,Human_Splice_Rec_2084395 RMVar_hsa_circ_70084,RMVar_hsa_circ_265887,RMVar_hsa_circ_19176,RMVar_hsa_circ_84895,RMVar_hsa_circ_87642,RMVar_hsa_circ_50346,RMVar_hsa_circ_64446,RMVar_hsa_circ_210204,RMVar_hsa_circ_210205,RMVar_hsa_circ_342474,RMVar_hsa_circ_362130,RMVar_hsa_circ_68449,RMVar_hsa_circ_11813,RMVar_hsa_circ_54815 67505 RMVar_ID_67505 Human_SNP_ID_681289811 m1A Human chr20 + 41489875 41489875 41489875 ACACAATGGCATTCATCTCTGTCCATGTCCGGAACTCCCGCTCCCAGTTAGTGATGGTGGAGAGA ACACAATGGCATTCATCTCTGTCCATGTCCGGCACTCCCGCTCCCAGTTAGTGATGGTGGAGAGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41488564..41491713 32194978 MeRIP-seq:(Medium) rs755114957 Functional Loss SNV dbSNP153 33..33 33 - - - 67506 RMVar_ID_67506 Human_SNP_ID_681290712 m1A Human chr20 - 41493581 41493581 41493581 GCTAGAGGAAGATGTAGATCCTGCAAAAGTTAAAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA GCTAGAGGAAGATGTAGATCCTGCAAAAGTTAGAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41491812..41493916 32194978 MeRIP-seq:(Medium) rs374043976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1929997,Human_RBP_ID_3960259,Human_RBP_ID_17700512,Human_RBP_ID_23002382 Human_Splice_Rec_2084290,Human_Splice_Rec_2084291,Human_Splice_Rec_2084356,Human_Splice_Rec_2084357,Human_Splice_Rec_2084382,Human_Splice_Rec_2084383 RMVar_hsa_circ_84895,RMVar_hsa_circ_210205,RMVar_hsa_circ_11813,RMVar_hsa_circ_3552,RMVar_hsa_circ_3712,RMVar_hsa_circ_47944,RMVar_hsa_circ_210208,RMVar_hsa_circ_299804,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_115660,RMVar_hsa_circ_210213,RMVar_hsa_circ_210214,RMVar_hsa_circ_305371,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_23471,RMVar_hsa_circ_210215,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210218,RMVar_hsa_circ_289090,RMVar_hsa_circ_363107 67507 RMVar_ID_67507 Human_SNP_ID_681290713 m1A Human chr20 - 41493581 41493581 41493581 GCTAGAGGAAGATGTAGATCCTGCAAAAGTTAAAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA GCTAGAGGAAGATGTAGATCCTGCAAAAGTTACAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA T G CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41491812..41493916 32194978 MeRIP-seq:(Medium) rs374043976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1929997,Human_RBP_ID_3960259,Human_RBP_ID_17700512,Human_RBP_ID_23002382 Human_Splice_Rec_2084290,Human_Splice_Rec_2084291,Human_Splice_Rec_2084356,Human_Splice_Rec_2084357,Human_Splice_Rec_2084382,Human_Splice_Rec_2084383 RMVar_hsa_circ_84895,RMVar_hsa_circ_210205,RMVar_hsa_circ_11813,RMVar_hsa_circ_3552,RMVar_hsa_circ_3712,RMVar_hsa_circ_47944,RMVar_hsa_circ_210208,RMVar_hsa_circ_299804,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_115660,RMVar_hsa_circ_210213,RMVar_hsa_circ_210214,RMVar_hsa_circ_305371,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_23471,RMVar_hsa_circ_210215,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210218,RMVar_hsa_circ_289090,RMVar_hsa_circ_363107 67508 RMVar_ID_67508 Human_SNP_ID_681291638 m1A Human chr20 - 41497474 41497474 41497474 GATAGTTCCTACTTACATTGTAAATGGGCCACAATGGAAGAGCTCGAAAAGGATCCTCGCATCGC GATAGTTCCTACTTACATTGTAAATGGGCCACGATGGAAGAGCTCGAAAAGGATCCTCGCATCGC T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41497378..41497479 32194978 MeRIP-seq:(Medium) rs764932222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2685533,Human_RBP_ID_3960845,Human_RBP_ID_9389308 Human_Splice_Rec_2084286,Human_Splice_Rec_2084287,Human_Splice_Rec_2084352,Human_Splice_Rec_2084353,Human_Splice_Rec_2084378,Human_Splice_Rec_2084379,Human_Splice_Rec_2084412 RMVar_hsa_circ_11813,RMVar_hsa_circ_3712,RMVar_hsa_circ_210208,RMVar_hsa_circ_299804,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_210214,RMVar_hsa_circ_305371,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_23471,RMVar_hsa_circ_210215,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210218,RMVar_hsa_circ_58352,RMVar_hsa_circ_289090,RMVar_hsa_circ_363107,RMVar_hsa_circ_25214,RMVar_hsa_circ_334431 67509 RMVar_ID_67509 Human_SNP_ID_681295377 m1A Human chr20 - 41512885 41512885 41512885 GAAACAATTGCTGTTCTTGGAGCTGGTCGAACATCTGCACTCTCAGCCTCTACACTGGCCTGGCA GAAACAATTGCTGTTCTTGGAGCTGGTCGAACGTCTGCACTCTCAGCCTCTACACTGGCCTGGCA T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41512882..41514842 32194978 MeRIP-seq:(Medium) rs778038126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62613,Human_RBP_ID_925858,Human_RBP_ID_3960846,Human_RBP_ID_5529142,Human_RBP_ID_8533701,Human_RBP_ID_9389311,Human_RBP_ID_18412924,Human_RBP_ID_18773412,Human_RBP_ID_22080675,Human_RBP_ID_26343007 Human_Splice_Rec_2084281,Human_Splice_Rec_2084407,Human_Splice_Rec_2084421 RMVar_hsa_circ_11813,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210219,RMVar_hsa_circ_92807,RMVar_hsa_circ_42420,RMVar_hsa_circ_25214,RMVar_hsa_circ_288967,RMVar_hsa_circ_294491,RMVar_hsa_circ_350353,RMVar_hsa_circ_280707,RMVar_hsa_circ_210221,RMVar_hsa_circ_210222,RMVar_hsa_circ_210220 67510 RMVar_ID_67510 Human_SNP_ID_681295378 m1A Human chr20 - 41512885 41512885 41512885 GAAACAATTGCTGTTCTTGGAGCTGGTCGAACATCTGCACTCTCAGCCTCTACACTGGCCTGGCA GAAACAATTGCTGTTCTTGGAGCTGGTCGAACCTCTGCACTCTCAGCCTCTACACTGGCCTGGCA T G CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41512882..41514842 32194978 MeRIP-seq:(Medium) rs778038126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62613,Human_RBP_ID_925858,Human_RBP_ID_3960846,Human_RBP_ID_5529142,Human_RBP_ID_8533701,Human_RBP_ID_9389311,Human_RBP_ID_18412924,Human_RBP_ID_18773412,Human_RBP_ID_22080675,Human_RBP_ID_26343007 Human_Splice_Rec_2084281,Human_Splice_Rec_2084407,Human_Splice_Rec_2084421 RMVar_hsa_circ_11813,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210219,RMVar_hsa_circ_92807,RMVar_hsa_circ_42420,RMVar_hsa_circ_25214,RMVar_hsa_circ_288967,RMVar_hsa_circ_294491,RMVar_hsa_circ_350353,RMVar_hsa_circ_280707,RMVar_hsa_circ_210221,RMVar_hsa_circ_210222,RMVar_hsa_circ_210220 67511 RMVar_ID_67511 Human_SNP_ID_681295878 m1A Human chr20 - 41514940 41514940 41514940 TTCTGAATTTCTCCTTGTAGCAAGGAGCAAGGACCAACCCCAGTGGAGAAAAAGAAGAAAGGAAA TTCTGAATTTCTCCTTGTAGCAAGGAGCAAGGTCCAACCCCAGTGGAGAAAAAGAAGAAAGGAAA T A CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:41514891..41515007 26863196 MeRIP-seq:(Medium) rs1307154321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62615,Human_RBP_ID_9347914,Human_RBP_ID_22080676,Human_RBP_ID_24546677,Human_RBP_ID_26343673 Human_Splice_Rec_2084278,Human_Splice_Rec_2084404,Human_Splice_Rec_2084418,Human_Splice_Rec_2084428 Human_miRNA_ID_2969849 RMVar_hsa_circ_11813,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_42420,RMVar_hsa_circ_25214,RMVar_hsa_circ_288967,RMVar_hsa_circ_294491,RMVar_hsa_circ_350353,RMVar_hsa_circ_280707,RMVar_hsa_circ_210221,RMVar_hsa_circ_210222,RMVar_hsa_circ_210220,RMVar_hsa_circ_210224,RMVar_hsa_circ_210223,RMVar_hsa_circ_373700 67512 RMVar_ID_67512 Human_SNP_ID_681300287 m1A Human chr20 - 41533278 41533278 41533278 AAAGGAGCCAGGAGACCAAGAGGGTGCAGCAAAGGGAAGCAAGGACAGAGAGCCCAAGCCAAAGA AAAGGAGCCAGGAGACCAAGAGGGTGCAGCAAGGGGAAGCAAGGACAGAGAGCCCAAGCCAAAGA T C CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:41533081..41533343 26863196 MeRIP-seq:(Medium) rs1402301894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831451,Human_RBP_ID_925862,Human_RBP_ID_9389316,Human_RBP_ID_18412926,Human_RBP_ID_18471132,Human_RBP_ID_19106541,Human_RBP_ID_23119605,Human_RBP_ID_24546680,Human_RBP_ID_26343013,Human_RBP_ID_27819814 Human_miRNA_ID_544729,Human_miRNA_ID_579966,Human_miRNA_ID_2193826,Human_miRNA_ID_2193827,Human_miRNA_ID_2208034,Human_miRNA_ID_2208035 RMVar_hsa_circ_210225,RMVar_hsa_circ_11813,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_42420,RMVar_hsa_circ_25214,RMVar_hsa_circ_288967,RMVar_hsa_circ_350353,RMVar_hsa_circ_280707,RMVar_hsa_circ_210221,RMVar_hsa_circ_210222,RMVar_hsa_circ_210224,RMVar_hsa_circ_273668,RMVar_hsa_circ_279993,RMVar_hsa_circ_360594,RMVar_hsa_circ_210226 67513 RMVar_ID_67513 Human_SNP_ID_681300365 m1A Human chr20 - 41533538 41533538 41533538 TTGTCAAATTTAAAAGTTTTGAATCACTCCCCAATGTCTGATGCCTCTGTCAATTTTGACTACAA TTGTCAAATTTAAAAGTTTTGAATCACTCCCCTATGTCTGATGCCTCTGTCAATTTTGACTACAA T A CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:41533487..41551322 26863196 MeRIP-seq:(Medium) rs749278751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4648273,Human_RBP_ID_9389320,Human_RBP_ID_18773415,Human_RBP_ID_26343015,Human_RBP_ID_27819817 Human_Splice_Rec_2084276,Human_Splice_Rec_2084416,Human_Splice_Rec_2084426,Human_Splice_Rec_2084432 Human_miRNA_ID_2368417,Human_miRNA_ID_2368418,Human_miRNA_ID_3016200,Human_miRNA_ID_3016201 RMVar_hsa_circ_210225,RMVar_hsa_circ_11813,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_42420,RMVar_hsa_circ_25214,RMVar_hsa_circ_288967,RMVar_hsa_circ_350353,RMVar_hsa_circ_280707,RMVar_hsa_circ_210221,RMVar_hsa_circ_210222,RMVar_hsa_circ_273668,RMVar_hsa_circ_279993,RMVar_hsa_circ_360594,RMVar_hsa_circ_210226 67514 RMVar_ID_67514 Human_SNP_ID_681319134 m1A Human chr20 + 41607012 41607012 41607012 CTCTGATGACTCCTCACAGCCAACACAAACCCAAACAACTCACCACGATCTTTAAAGCCTTTCTC CTCTGATGACTCCTCACAGCCAACACAAACCCCAACAACTCACCACGATCTTTAAAGCCTTTCTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:41606988..41607104 26863196 MeRIP-seq:(Medium) rs1490175161 Functional Loss SNV dbSNP153 33..33 33 - - - 67515 RMVar_ID_67515 Human_SNP_ID_681319135 m1A Human chr20 + 41607016 41607016 41607016 GATGACTCCTCACAGCCAACACAAACCCAAACAACTCACCACGATCTTTAAAGCCTTTCTCAACA GATGACTCCTCACAGCCAACACAAACCCAAACCACTCACCACGATCTTTAAAGCCTTTCTCAACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:41606975..41607143 26863196 MeRIP-seq:(Medium) rs1037703700 Functional Loss SNV dbSNP153 33..33 33 - - - 67516 RMVar_ID_67516 Human_SNP_ID_681783418 m1A Human chr20 + 43458459 43458459 43458459 GGAGCTCTGCGGCGAGCGCGTGATCGTAGAGCACGCCCGGGGCCCGCGTCGCGATCGCGACGGCT GGAGCTCTGCGGCGAGCGCGTGATCGTAGAGCCCGCCCGGGGCCCGCGTCGCGATCGCGACGGCT A C AL031681.3,SRSF6 Ensembl:ENSG00000288000,Ensembl:ENSG00000124193 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:43458423..43458563 26863196 MeRIP-seq:(Medium) rs1348637885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564363,Human_RBP_ID_4648388,Human_RBP_ID_7003224,Human_RBP_ID_9390775,Human_RBP_ID_14113006,Human_RBP_ID_17972107,Human_RBP_ID_18773506,Human_RBP_ID_19106549,Human_RBP_ID_23004778,Human_RBP_ID_23115405,Human_RBP_ID_23119685 Human_Splice_Rec_2085046,Human_Splice_Rec_2085047,Human_Splice_Rec_2085058,Human_Splice_Rec_2085059,Human_Splice_Rec_2085068,Human_Splice_Rec_2085069,Human_Splice_Rec_2085078,Human_Splice_Rec_2085079,Human_Splice_Rec_2085088,Human_Splice_Rec_2085089,Human_Splice_Rec_2085110,Human_Splice_Rec_2085111 Human_miRNA_ID_2296478 RMVar_hsa_circ_123199,RMVar_hsa_circ_210239 67517 RMVar_ID_67517 Human_SNP_ID_681783514 m1A Human chr20 + 43458646 43458646 43458646 TGACTTGGGTGTCCCCGAGCCCCGCTGCCTTCACGTCTGCCCGGGGCAGCCATGGGACGCCGGAG TGACTTGGGTGTCCCCGAGCCCCGCTGCCTTCGCGTCTGCCCGGGGCAGCCATGGGACGCCGGAG A G AL031681.3,SRSF6 Ensembl:ENSG00000288000,Ensembl:ENSG00000124193 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43458644..43458827 26863196 MeRIP-seq:(Medium) rs1309139989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779844,Human_RBP_ID_5383812,Human_RBP_ID_8204015,Human_RBP_ID_9430812,Human_RBP_ID_18950633,Human_RBP_ID_26787705 Human_Splice_Rec_2085099 67518 RMVar_ID_67518 Human_SNP_ID_681784325 m1A Human chr20 + 43460913 43460913 43460913 GGAAAGGGTGATATAAAGTCAAAATCCAGATCAAGGAGCCAGTCCCGTTCCAATTCGCCGCTACC GGAAAGGGTGATATAAAGTCAAAATCCAGATCGAGGAGCCAGTCCCGTTCCAATTCGCCGCTACC A G AL031681.3,SRSF6 Ensembl:ENSG00000288000,Ensembl:ENSG00000124193 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:43460862..43460974 26863196 MeRIP-seq:(Medium) rs780715218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1597433,Human_RBP_ID_1930086,Human_RBP_ID_3649214,Human_RBP_ID_14113082,Human_RBP_ID_22817584,Human_RBP_ID_23002466 Human_miRNA_ID_477608,Human_miRNA_ID_2084518 RMVar_hsa_circ_78488,RMVar_hsa_circ_210240,RMVar_hsa_circ_109694,RMVar_hsa_circ_210242,RMVar_hsa_circ_90777,RMVar_hsa_circ_91396,RMVar_hsa_circ_210243,RMVar_hsa_circ_210244 67519 RMVar_ID_67519 Human_SNP_ID_681798795 m1A Human chr20 + 43514486 43514486 43514486 GGCGTAGCCTGGAGTGAGGGTTTGGCTGGTGTAGCTTGGAGTGAGGCCCCCTGGCGTGGAGTCTT GGCGTAGCCTGGAGTGAGGGTTTGGCTGGTGTGGCTTGGAGTGAGGCCCCCTGGCGTGGAGTCTT A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:43514437..43514546 26863196 MeRIP-seq:(Medium) rs1189777902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924027,Human_RBP_ID_3960262,Human_RBP_ID_5383813,Human_RBP_ID_5529449,Human_RBP_ID_14113457,Human_RBP_ID_18412857,Human_RBP_ID_18422895,Human_RBP_ID_19109545,Human_RBP_ID_21982992,Human_RBP_ID_22258543,Human_RBP_ID_23004978,Human_RBP_ID_23906024,Human_RBP_ID_26344056 Human_Splice_Rec_2085160 RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_210247 67520 RMVar_ID_67520 Human_SNP_ID_681798838 m1A Human chr20 + 43514554 43514554 43514554 GCCTGCTGAGGGCGTGAGCTGGCATGAGGCGAAGAGAGGGCCATGGCACCGACTCCGAGATGGGT GCCTGCTGAGGGCGTGAGCTGGCATGAGGCGAGGAGAGGGCCATGGCACCGACTCCGAGATGGGT A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43514350..43515082 26863196 MeRIP-seq:(Medium) rs1304586046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924907,Human_RBP_ID_3960262,Human_RBP_ID_18422895,Human_RBP_ID_21982992,Human_RBP_ID_23004978,Human_RBP_ID_26344056 RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_210247 67521 RMVar_ID_67521 Human_SNP_ID_681798946 m1A Human chr20 - 43514751 43514751 43514751 CTCCTACCCGCCTGTTGGGGGCCCGCCTCGCCATCTCCCGCCGGGGCCCCGCCATCTTCGTATTC CTCCTACCCGCCTGTTGGGGGCCCGCCTCGCCGTCTCCCGCCGGGGCCCCGCCATCTTCGTATTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:43514336..43514885 26863196 MeRIP-seq:(Medium) rs750696565 Functional Loss SNV dbSNP153 33..33 33 - - - 67522 RMVar_ID_67522 Human_SNP_ID_681805484 m1A Human chr20 + 43539028 43539028 43539028 GGGTATGGGCAGGTATTAGGATTTCGCTGATGAACAGAGAGAGCAGCAGGAAGGCAGTGGCACAG GGGTATGGGCAGGTATTAGGATTTCGCTGATGGACAGAGAGAGCAGCAGGAAGGCAGTGGCACAG A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43539014..43539142 26863196 MeRIP-seq:(Medium) rs1019020694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14113805 RMVar_hsa_circ_210251,RMVar_hsa_circ_307618,RMVar_hsa_circ_210250,RMVar_hsa_circ_109630,RMVar_hsa_circ_210254 67523 RMVar_ID_67523 Human_SNP_ID_681818710 m1A Human chr20 - 43591026 43591026 43591026 TTACCTGAGGCCCAGCGACCACCGCTCACCTGACGCCGCCCAGCATCCCGCGGCCAGGTATCCAA TTACCTGAGGCCCAGCGACCACCGCTCACCTGCCGCCGCCCAGCATCCCGCGGCCAGGTATCCAA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:43590965..43591102 26863410 MeRIP-seq:(Medium) rs536758906 Functional Loss SNV dbSNP153 33..33 33 - - - 67524 RMVar_ID_67524 Human_SNP_ID_681818711 m1A Human chr20 - 43591031 43591031 43591031 GCCCTTTACCTGAGGCCCAGCGACCACCGCTCACCTGACGCCGCCCAGCATCCCGCGGCCAGGTA GCCCTTTACCTGAGGCCCAGCGACCACCGCTCTCCTGACGCCGCCCAGCATCCCGCGGCCAGGTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43590993..43591098 26863196 MeRIP-seq:(Medium) rs918664595 Functional Loss SNV dbSNP153 33..33 33 - - - 67525 RMVar_ID_67525 Human_SNP_ID_681840225 m1A Human chr20 + 43673820 43673820 43673820 GGCCTGCTTTCCCCATAGCGAGGATCTGGATGAGCTGCACTACCAGGACACAGATTCAGATGTGC GGCCTGCTTTCCCCATAGCGAGGATCTGGATGCGCTGCACTACCAGGACACAGATTCAGATGTGC A C MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr20:43673801..43673900;chr20:43673801..43673825 26863196 MeRIP-seq:(Medium) rs368379152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1026162,Human_RBP_ID_1597508,Human_RBP_ID_1930146,Human_RBP_ID_3649311,Human_RBP_ID_4659409,Human_RBP_ID_5200073,Human_RBP_ID_8533890,Human_RBP_ID_8854943,Human_RBP_ID_9331888,Human_RBP_ID_9389329,Human_RBP_ID_14114440,Human_RBP_ID_17143577,Human_RBP_ID_17976363,Human_RBP_ID_18773600,Human_RBP_ID_22452780,Human_RBP_ID_27564573 Human_Splice_Rec_2086268,Human_Splice_Rec_2086269,Human_Splice_Rec_2086292,Human_Splice_Rec_2086293 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210272,RMVar_hsa_circ_346978,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_349961,RMVar_hsa_circ_374244,RMVar_hsa_circ_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_210271 67526 RMVar_ID_67526 Human_SNP_ID_681840239 m1A Human chr20 + 43673856 43673856 43673856 GCACTACCAGGACACAGATTCAGATGTGCCGGAGCAGAGGGATAGCAAGTGCAAGGTCAAATGGA GCACTACCAGGACACAGATTCAGATGTGCCGGGGCAGAGGGATAGCAAGTGCAAGGTCAAATGGA A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:43673801..43673900 32194978 MeRIP-seq:(Medium) rs1265958742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1597509,Human_RBP_ID_1930147,Human_RBP_ID_4659851,Human_RBP_ID_7003600,Human_RBP_ID_8533891,Human_RBP_ID_9331888,Human_RBP_ID_9389329,Human_RBP_ID_14114442,Human_RBP_ID_17281556,Human_RBP_ID_18773603,Human_RBP_ID_22817599,Human_RBP_ID_23005201 Human_Splice_Rec_2086268,Human_Splice_Rec_2086269,Human_Splice_Rec_2086292,Human_Splice_Rec_2086293 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210272,RMVar_hsa_circ_346978,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_349961,RMVar_hsa_circ_374244,RMVar_hsa_circ_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_210271 67527 RMVar_ID_67527 Human_SNP_ID_681840248 m1A Human chr20 - 43673893 43673893 43673893 AACCCTCTCTTCCCCATGGCACTCACCTCCTCATGGGTCCATTTGACCTTGCACTTGCTATCCCT AACCCTCTCTTCCCCATGGCACTCACCTCCTCGTGGGTCCATTTGACCTTGCACTTGCTATCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:43673757..43673975;chr20:43673743..43673958 26863196 MeRIP-seq:(Medium) rs966481281 Functional Loss SNV dbSNP153 33..33 33 - - - 67528 RMVar_ID_67528 Human_SNP_ID_681841821 m1A Human chr20 - 43678916 43678916 43678916 CCTGGCACAGCGCCCTCTCCCACTCCCTCAGCACTGGTCTCTCAGCCCCAGCCTGTGCTCTATAT CCTGGCACAGCGCCCTCTCCCACTCCCTCAGCGCTGGTCTCTCAGCCCCAGCCTGTGCTCTATAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:43678915..43679116 26863196 MeRIP-seq:(Medium) rs1306051213 Functional Loss SNV dbSNP153 33..33 33 - - - 67529 RMVar_ID_67529 Human_SNP_ID_681841827 m1A Human chr20 + 43678931 43678931 43678931 TGGGGCTGAGAGACCAGTGCTGAGGGAGTGGGAGAGGGCGCTGTGCCAGGCAAGCAAGAGGTGGC TGGGGCTGAGAGACCAGTGCTGAGGGAGTGGGTGAGGGCGCTGTGCCAGGCAAGCAAGAGGTGGC A T MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43678928..43679154 26863196 MeRIP-seq:(Medium) rs945547097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114551,Human_RBP_ID_23906181 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210272,RMVar_hsa_circ_346978,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_349961,RMVar_hsa_circ_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273 67530 RMVar_ID_67530 Human_SNP_ID_681844059 m1A Human chr20 - 43686978 43686978 43686978 GATGATGCGGTCCTCCTCCTCGGTCCAGCAAGACTTCTTCACCTCAGGGTTGAGGTGGTTGTGCC GATGATGCGGTCCTCCTCCTCGGTCCAGCAAGTCTTCTTCACCTCAGGGTTGAGGTGGTTGTGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:43686928..43687009 26863196 MeRIP-seq:(Medium) rs770579437 Functional Loss SNV dbSNP153 33..33 33 - - - 67531 RMVar_ID_67531 Human_SNP_ID_681847723 m1A Human chr20 + 43699841 43699841 43699841 AAAACAGTGAGGAGGAACTTGCAGCAGCCACCACATCGAAGGAACAGGAGCCCATCGGTACAGAT AAAACAGTGAGGAGGAACTTGCAGCAGCCACCGCATCGAAGGAACAGGAGCCCATCGGTACAGAT A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:43699791..43700080 26863196 MeRIP-seq:(Medium) rs758794739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564509,Human_RBP_ID_1597540,Human_RBP_ID_1930170,Human_RBP_ID_3649344,Human_RBP_ID_4648551,Human_RBP_ID_7003689,Human_RBP_ID_8260405,Human_RBP_ID_8533918,Human_RBP_ID_8854952,Human_RBP_ID_14114908,Human_RBP_ID_17281560,Human_RBP_ID_17511703,Human_RBP_ID_17700527,Human_RBP_ID_27297338 Human_Splice_Rec_2086276,Human_Splice_Rec_2086302 Human_miRNA_ID_1979653 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_53095,RMVar_hsa_circ_19587,RMVar_hsa_circ_92301,RMVar_hsa_circ_210276,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_297485,RMVar_hsa_circ_348575,RMVar_hsa_circ_284606,RMVar_hsa_circ_17214,RMVar_hsa_circ_210278,RMVar_hsa_circ_76011,RMVar_hsa_circ_210279,RMVar_hsa_circ_210277,RMVar_hsa_circ_371701,RMVar_hsa_circ_84691,RMVar_hsa_circ_210281,RMVar_hsa_circ_210282 67532 RMVar_ID_67532 Human_SNP_ID_681848484 m1A Human chr20 + 43702675 43702675 43702675 ACCGAGTACCGCCTGGATGGCCACACCATCTCAGACCTGAGCCGGAGCAGCCGGGGCGAGCTGAT ACCGAGTACCGCCTGGATGGCCACACCATCTCTGACCTGAGCCGGAGCAGCCGGGGCGAGCTGAT A T MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:43702626..43702800 32194978 MeRIP-seq:(Medium) rs1450471241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564516,Human_RBP_ID_1930178,Human_RBP_ID_3960858,Human_RBP_ID_8533928,Human_RBP_ID_18193658,Human_RBP_ID_26820877,Human_RBP_ID_27486025,Human_RBP_ID_27564574 Human_miRNA_ID_302228,Human_miRNA_ID_1382208,Human_miRNA_ID_2270647 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_92301,RMVar_hsa_circ_210276,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_297485,RMVar_hsa_circ_348575,RMVar_hsa_circ_17214,RMVar_hsa_circ_210278,RMVar_hsa_circ_76011,RMVar_hsa_circ_210277,RMVar_hsa_circ_371701,RMVar_hsa_circ_84691,RMVar_hsa_circ_210281,RMVar_hsa_circ_210286,RMVar_hsa_circ_124852,RMVar_hsa_circ_298756,RMVar_hsa_circ_371245,RMVar_hsa_circ_210282,RMVar_hsa_circ_307993,RMVar_hsa_circ_275164,RMVar_hsa_circ_210288,RMVar_hsa_circ_96591,RMVar_hsa_circ_210287,RMVar_hsa_circ_210284,RMVar_hsa_circ_210285,RMVar_hsa_circ_210283 67533 RMVar_ID_67533 Human_SNP_ID_681848533 m1A Human chr20 - 43702799 43702799 43702799 GGACAGACTGGTGCTATTCTCAGTGACAGGGGACAGAGCCACACGCCTCTTCCTCTGCCGCTTGA GGACAGACTGGTGCTATTCTCAGTGACAGGGGGCAGAGCCACACGCCTCTTCCTCTGCCGCTTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:43702751..43702925 32194978 MeRIP-seq:(Medium) rs1470855293 Functional Loss SNV dbSNP153 33..33 33 - - - 67534 RMVar_ID_67534 Human_SNP_ID_681848546 m1A Human chr20 + 43702847 43702847 43702847 ATAGCACCAGTCTGTCCTTCCTGGATTCCTGTAACAGCCTCACGCCCAAGAGCACACCTGTTAAG ATAGCACCAGTCTGTCCTTCCTGGATTCCTGTGACAGCCTCACGCCCAAGAGCACACCTGTTAAG A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1325560725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1380307,Human_RBP_ID_1597558,Human_RBP_ID_1930181,Human_RBP_ID_3649354,Human_RBP_ID_8533932,Human_RBP_ID_14114955,Human_RBP_ID_17281563,Human_RBP_ID_17395523,Human_RBP_ID_17511707,Human_RBP_ID_18773667,Human_RBP_ID_22817606,Human_RBP_ID_27021512,Human_RBP_ID_27486027 Human_Splice_Rec_2086279,Human_Splice_Rec_2086305 Human_miRNA_ID_2716588,Human_miRNA_ID_3052572 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_92301,RMVar_hsa_circ_210276,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_297485,RMVar_hsa_circ_348575,RMVar_hsa_circ_17214,RMVar_hsa_circ_210278,RMVar_hsa_circ_76011,RMVar_hsa_circ_210277,RMVar_hsa_circ_371701,RMVar_hsa_circ_84691,RMVar_hsa_circ_210281,RMVar_hsa_circ_210286,RMVar_hsa_circ_124852,RMVar_hsa_circ_298756,RMVar_hsa_circ_371245,RMVar_hsa_circ_210282,RMVar_hsa_circ_307993,RMVar_hsa_circ_275164,RMVar_hsa_circ_210288,RMVar_hsa_circ_96591,RMVar_hsa_circ_210287,RMVar_hsa_circ_210284,RMVar_hsa_circ_210285,RMVar_hsa_circ_210283 67535 RMVar_ID_67535 Human_SNP_ID_681849207 m1A Human chr20 + 43705246 43705246 43705246 GGCAGTTTCTGAACTTCTGGAACAAACAGGACACATTGGAGCTGGAGAGCCCCTCGCTGACATCC GGCAGTTTCTGAACTTCTGGAACAAACAGGACGCATTGGAGCTGGAGAGCCCCTCGCTGACATCC A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1219063492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1597562,Human_RBP_ID_1930183,Human_RBP_ID_3649355,Human_RBP_ID_4663897,Human_RBP_ID_7003701,Human_RBP_ID_8533935,Human_RBP_ID_8854965,Human_RBP_ID_14114992,Human_RBP_ID_17281564,Human_RBP_ID_17395524,Human_RBP_ID_17511709,Human_RBP_ID_17700529,Human_RBP_ID_17972207,Human_RBP_ID_18773671,Human_RBP_ID_23133718 Human_Splice_Rec_2086280,Human_Splice_Rec_2086306 Human_miRNA_ID_2391374 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_210276,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_297485,RMVar_hsa_circ_348575,RMVar_hsa_circ_17214,RMVar_hsa_circ_76011,RMVar_hsa_circ_210277,RMVar_hsa_circ_84691,RMVar_hsa_circ_102413,RMVar_hsa_circ_210286,RMVar_hsa_circ_124852,RMVar_hsa_circ_298756,RMVar_hsa_circ_371245,RMVar_hsa_circ_210282,RMVar_hsa_circ_275164,RMVar_hsa_circ_210288,RMVar_hsa_circ_96591,RMVar_hsa_circ_210287,RMVar_hsa_circ_210284,RMVar_hsa_circ_210285,RMVar_hsa_circ_210289 67536 RMVar_ID_67536 Human_SNP_ID_681921654 m1A Human chr20 - 44006582 44006582 44006582 GGGAGGTTGGGAGGTGTTATCGGGGGGATCTCATAGTCTTCGTTGTTCTCGCTCTGGCCGTTGTA GGGAGGTTGGGAGGTGTTATCGGGGGGATCTCTTAGTCTTCGTTGTTCTCGCTCTGGCCGTTGTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44006552..44006697 26863196 MeRIP-seq:(Medium) rs1249508315 Functional Loss SNV dbSNP153 33..33 33 - - - 67537 RMVar_ID_67537 Human_SNP_ID_681921684 m1A Human chr20 + 44006641 44006641 44006641 CCTCCCGGAGCCATCCCTCCTGCACCTGGGGGACCACGAAGCCAGCTACCACTCGCTGTGCCACG CCTCCCGGAGCCATCCCTCCTGCACCTGGGGGGCCACGAAGCCAGCTACCACTCGCTGTGCCACG A G TOX2 Ensembl:ENSG00000124191 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:44006502..44006725 26863196 MeRIP-seq:(Medium) rs1174645856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2086324,Human_Splice_Rec_2086340,Human_Splice_Rec_2086358,Human_Splice_Rec_2086374 RMVar_hsa_circ_8876,RMVar_hsa_circ_37750,RMVar_hsa_circ_103865,RMVar_hsa_circ_210294,RMVar_hsa_circ_285899,RMVar_hsa_circ_96996,RMVar_hsa_circ_210296,RMVar_hsa_circ_210297,RMVar_hsa_circ_210295,RMVar_hsa_circ_308886 67538 RMVar_ID_67538 Human_SNP_ID_681937435 m1A Human chr20 - 44068947 44068947 44068947 CAGACATAGGGTACCGTGCGCAGGGCGAGGACAGGGTCCACAGTTACCCTGGAGCAAGCAGGTCA CAGACATAGGGTACCGTGCGCAGGGCGAGGACGGGGTCCACAGTTACCCTGGAGCAAGCAGGTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44068898..44069039 26863196 MeRIP-seq:(Medium) rs1203570954 Functional Loss SNV dbSNP153 33..33 33 - - - 67539 RMVar_ID_67539 Human_SNP_ID_681949272 m1A Human chr20 - 44115853 44115853 44115853 CGTCCCCGGCCACCGCCCCGCTGCAGGCCCCCACGCTCCGAGGCCCCGAGCCTGCACGCGAGACC CGTCCCCGGCCACCGCCCCGCTGCAGGCCCCCGCGCTCCGAGGCCCCGAGCCTGCACGCGAGACC T C JPH2 Ensembl:ENSG00000149596 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44115807..44115887 26863196 MeRIP-seq:(Medium) rs1478428525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80253,RMVar_hsa_circ_210301 67540 RMVar_ID_67540 Human_SNP_ID_681949283 m1A Human chr20 - 44115874 44115874 44115874 CCGGGTCCGAGTCCGCGCCCTCGTCCCCGGCCACCGCCCCGCTGCAGGCCCCCACGCTCCGAGGC CCGGGTCCGAGTCCGCGCCCTCGTCCCCGGCCGCCGCCCCGCTGCAGGCCCCCACGCTCCGAGGC T C JPH2 Ensembl:ENSG00000149596 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44115826..44116000 26863196 MeRIP-seq:(Medium) rs1404231819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80253,RMVar_hsa_circ_210301 67541 RMVar_ID_67541 Human_SNP_ID_681953727 m1A Human chr20 + 44132506 44132504 44132506 TGCCCAGGGAGATCATCTCTACAGCCTGCATCACTAGCTCCCTTGCTCACTGGCTTCCAGTGCGC TGCCCAGGGAGATCATCTCTACAGCCTGCAT__CTAGCTCCCTTGCTCACTGGCTTCCAGTGCGC TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44132504..44132618 26863196 MeRIP-seq:(Medium) rs1159494806 Functional Loss DEL dbSNP153 32..33 33 - - - 67542 RMVar_ID_67542 Human_SNP_ID_681953728 m1A Human chr20 + 44132506 44132505 44132506 TGCCCAGGGAGATCATCTCTACAGCCTGCATCACTAGCTCCCTTGCTCACTGGCTTCCAGTGCGC TGCCCAGGGAGATCATCTCTACAGCCTGCATC_CTAGCTCCCTTGCTCACTGGCTTCCAGTGCGC CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44132504..44132618 26863196 MeRIP-seq:(Medium) rs1303537648 Functional Loss DEL dbSNP153 33..33 33 - - - 67543 RMVar_ID_67543 Human_SNP_ID_681972893 m1A Human chr20 + 44203069 44203069 44203069 CACCTGTGCCTTCTCCAACAGACAGAGATGCTACAGACCTGAAGACAAGAACAAAGTTTACAGCT CACCTGTGCCTTCTCCAACAGACAGAGATGCTGCAGACCTGAAGACAAGAACAAAGTTTACAGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:44197424..44206990 32194978 MeRIP-seq:(Medium) rs764555069 Functional Loss SNV dbSNP153 33..33 33 - - - 67544 RMVar_ID_67544 Human_SNP_ID_681974787 m1A Human chr20 + 44210232 44210232 44210232 GGGCACTGCCCGCCCGGGGTCTCCAGCTGTGAAGTTGCGCTCCTCGGGAGATTCCTGGGGTCAGA GGGCACTGCCCGCCCGGGGTCTCCAGCTGTGAGGTTGCGCTCCTCGGGAGATTCCTGGGGTCAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44210230..44210533 26863196 MeRIP-seq:(Medium) rs1423955536 Functional Loss SNV dbSNP153 33..33 33 - - - 67545 RMVar_ID_67545 Human_SNP_ID_681974824 m1A Human chr20 - 44210344 44210344 44210344 TTCCAGTCCTTTCTCTCTCGCCTCGGAGCCCCATTCTCTTTGGCTACCTCTTCGGCCCCACTCCT TTCCAGTCCTTTCTCTCTCGCCTCGGAGCCCCGTTCTCTTTGGCTACCTCTTCGGCCCCACTCCT T C OSER1 Ensembl:ENSG00000132823 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:44210312..44210549 26863410 MeRIP-seq:(Medium) rs940732606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132525,Human_RBP_ID_5323263,Human_RBP_ID_5385210,Human_RBP_ID_18950646,Human_RBP_ID_20624173 67546 RMVar_ID_67546 Human_SNP_ID_681975014 m1A Human chr20 + 44210742 44210742 44210742 GACGCTCCGGTGATGCGGGGCAGTCAGTTCAGAGCGTCTCTCCCAAATCTCGGCACCCGACTGAC GACGCTCCGGTGATGCGGGGCAGTCAGTTCAGGGCGTCTCTCCCAAATCTCGGCACCCGACTGAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44210644..44210775 26863196 MeRIP-seq:(Medium) rs1569246303 Functional Loss SNV dbSNP153 33..33 33 - - - 67547 RMVar_ID_67547 Human_SNP_ID_681975018 m1A Human chr20 - 44210746 44210746 44210746 CCGGGTCAGTCGGGTGCCGAGATTTGGGAGAGACGCTCTGAACTGACTGCCCCGCATCACCGGAG CCGGGTCAGTCGGGTGCCGAGATTTGGGAGAGGCGCTCTGAACTGACTGCCCCGCATCACCGGAG T C OSER1 Ensembl:ENSG00000132823 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:44210665..44210754;chr20:44210635..44210775;chr20:44210641..44210775 26863196 MeRIP-seq:(Medium) rs1033913023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1597681,Human_RBP_ID_5503391,Human_RBP_ID_17700532,Human_RBP_ID_22081362 Human_Splice_Rec_2086415 67548 RMVar_ID_67548 Human_SNP_ID_681999083 m1A Human chr20 - 44311144 44311144 44311144 AGGAGGACGGTGGCTGACGAGATCCGGCATGGAGCATCTGGAGCGCTGCGAGTGGTTGTTGCGGG AGGAGGACGGTGGCTGACGAGATCCGGCATGGTGCATCTGGAGCGCTGCGAGTGGTTGTTGCGGG T A FITM2 Ensembl:ENSG00000197296 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:44307112..44311245;chr20:44307233..44311180 26863196 MeRIP-seq:(Medium) rs1282784774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779487,Human_RBP_ID_4660435 67549 RMVar_ID_67549 Human_SNP_ID_682040519 m1A Human chr20 - 44475984 44475984 44475984 CACGGATGGGCTCGCGGGCACTCACCGGCCCGACTACGGGCGGAGCGCGGGTCAATCGGCGGCGG CACGGATGGGCTCGCGGGCACTCACCGGCCCGCCTACGGGCGGAGCGCGGGTCAATCGGCGGCGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:44475939..44476155 26863196 MeRIP-seq:(Medium) rs1435440304 Functional Loss SNV dbSNP153 33..33 33 - - - 67550 RMVar_ID_67550 Human_SNP_ID_682046236 m1A Human chr20 - 44498887 44498887 44498887 TAAAACTGCATGTTAAAGGCAGGAAGATGGGGAAAAAAAGTTCAGTAAAGCTGGAATGGGGAAAT TAAAACTGCATGTTAAAGGCAGGAAGATGGGGGAAAAAAGTTCAGTAAAGCTGGAATGGGGAAAT T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44498838..44499062 26863196 MeRIP-seq:(Medium) rs1304903332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4648879,Human_RBP_ID_7004270,Human_RBP_ID_18773783,Human_RBP_ID_23906453 RMVar_hsa_circ_96393,RMVar_hsa_circ_210310 67551 RMVar_ID_67551 Human_SNP_ID_682046554 m1A Human chr20 - 44500326 44500326 44500326 CTCCTGCTTTACGTCTGGACCCTTGTGGCTCCACTTGTCCTCACCAGTCGGGACTTCAGCTGAAC CTCCTGCTTTACGTCTGGACCCTTGTGGCTCCCCTTGTCCTCACCAGTCGGGACTTCAGCTGAAC T G SERINC3 Ensembl:ENSG00000132824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:44500276..44500350 32194978 MeRIP-seq:(Medium) rs766121805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564700,Human_RBP_ID_779143,Human_RBP_ID_927169,Human_RBP_ID_8534077,Human_RBP_ID_8855105,Human_RBP_ID_9298092,Human_RBP_ID_14116083,Human_RBP_ID_17281613,Human_RBP_ID_17396748,Human_RBP_ID_17513013,Human_RBP_ID_22452781,Human_RBP_ID_22767129 Human_Splice_Rec_2086775,Human_Splice_Rec_2086795 Human_miRNA_ID_1962871,Human_miRNA_ID_1962872 RMVar_hsa_circ_79966,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210311,RMVar_hsa_circ_320099,RMVar_hsa_circ_210312 67552 RMVar_ID_67552 Human_SNP_ID_682046593 m1A Human chr20 - 44500424 44500424 44500424 TGACTCTCTCTTGTTTTCTTAGCCCTGATGCAAAGTTTCAGAGCATGACCAGCAAGTGGCCAGCT TGACTCTCTCTTGTTTTCTTAGCCCTGATGCAGAGTTTCAGAGCATGACCAGCAAGTGGCCAGCT T C SERINC3 Ensembl:ENSG00000132824 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1254122914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779144,Human_RBP_ID_924039,Human_RBP_ID_22767130 Human_Splice_Rec_2086774,Human_Splice_Rec_2086794,Human_Splice_Rec_2086814 Human_miRNA_ID_881569,Human_miRNA_ID_2908786,Human_miRNA_ID_2908787,Human_miRNA_ID_3027627,Human_miRNA_ID_3027628 RMVar_hsa_circ_79966,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210311,RMVar_hsa_circ_320099,RMVar_hsa_circ_210312 67553 RMVar_ID_67553 Human_SNP_ID_682047466 m1A Human chr20 + 44503949 44503949 44503949 GCAGTTGAATTTCCAGGAGCCAGGGTTGGTGCAGTTATGCGTGTAATAAAGCTCATCAGGTTGGG GCAGTTGAATTTCCAGGAGCCAGGGTTGGTGCGGTTATGCGTGTAATAAAGCTCATCAGGTTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44503899..44504042 26863196 MeRIP-seq:(Medium) rs146595453 Functional Loss SNV dbSNP153 33..33 33 - - - 67554 RMVar_ID_67554 Human_SNP_ID_682066400 m1A Human chr20 + 44582543 44582543 44582543 TACAACAAATGGGGACTTACTTGGCCCGAGACATGGGAAACACCCACTAAAACCTCAAAGTGCTT TACAACAAATGGGGACTTACTTGGCCCGAGACGTGGGAAACACCCACTAAAACCTCAAAGTGCTT A G PKIG Ensembl:ENSG00000168734 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44582539..44582662 26863196 MeRIP-seq:(Medium) rs1006682650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87348,RMVar_hsa_circ_210328 67555 RMVar_ID_67555 Human_SNP_ID_682066401 m1A Human chr20 + 44582543 44582543 44582543 TACAACAAATGGGGACTTACTTGGCCCGAGACATGGGAAACACCCACTAAAACCTCAAAGTGCTT TACAACAAATGGGGACTTACTTGGCCCGAGACTTGGGAAACACCCACTAAAACCTCAAAGTGCTT A T PKIG Ensembl:ENSG00000168734 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44582539..44582662 26863196 MeRIP-seq:(Medium) rs1006682650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87348,RMVar_hsa_circ_210328 67556 RMVar_ID_67556 Human_SNP_ID_682067934 m1A Human chr20 + 44589846 44589846 44589846 GTCAACAGTGGAAAATCTGAAGAGATGCAAGCAGGAAAAAGAAATTAAACCAGGTAGGTAGTGGC GTCAACAGTGGAAAATCTGAAGAGATGCAAGCGGGAAAAAGAAATTAAACCAGGTAGGTAGTGGC A G PKIG Ensembl:ENSG00000168734 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr20:44589776..44589850;chr20:44589747..44589875;chr20:44589776..44589875;chr20:44585181..44598623 26863196,32194978 MeRIP-seq:(Medium) rs958249031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925906,Human_RBP_ID_1930289,Human_RBP_ID_19005890 Human_Splice_Rec_2086820,Human_Splice_Rec_2086821,Human_Splice_Rec_2086828,Human_Splice_Rec_2086829,Human_Splice_Rec_2086838,Human_Splice_Rec_2086839,Human_Splice_Rec_2086846,Human_Splice_Rec_2086847,Human_Splice_Rec_2086856,Human_Splice_Rec_2086857,Human_Splice_Rec_2086862,Human_Splice_Rec_2086863,Human_Splice_Rec_2086866,Human_Splice_Rec_2086867 RMVar_hsa_circ_28750,RMVar_hsa_circ_87348,RMVar_hsa_circ_109947,RMVar_hsa_circ_210328,RMVar_hsa_circ_313962,RMVar_hsa_circ_210329,RMVar_hsa_circ_210330,RMVar_hsa_circ_332693 67557 RMVar_ID_67557 Human_SNP_ID_682067935 m1A Human chr20 + 44589846 44589846 44589846 GTCAACAGTGGAAAATCTGAAGAGATGCAAGCAGGAAAAAGAAATTAAACCAGGTAGGTAGTGGC GTCAACAGTGGAAAATCTGAAGAGATGCAAGCTGGAAAAAGAAATTAAACCAGGTAGGTAGTGGC A T PKIG Ensembl:ENSG00000168734 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr20:44589776..44589850;chr20:44589747..44589875;chr20:44589776..44589875;chr20:44585181..44598623 26863196,32194978 MeRIP-seq:(Medium) rs958249031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925906,Human_RBP_ID_1930289,Human_RBP_ID_19005890 Human_Splice_Rec_2086820,Human_Splice_Rec_2086821,Human_Splice_Rec_2086828,Human_Splice_Rec_2086829,Human_Splice_Rec_2086838,Human_Splice_Rec_2086839,Human_Splice_Rec_2086846,Human_Splice_Rec_2086847,Human_Splice_Rec_2086856,Human_Splice_Rec_2086857,Human_Splice_Rec_2086862,Human_Splice_Rec_2086863,Human_Splice_Rec_2086866,Human_Splice_Rec_2086867 RMVar_hsa_circ_28750,RMVar_hsa_circ_87348,RMVar_hsa_circ_109947,RMVar_hsa_circ_210328,RMVar_hsa_circ_313962,RMVar_hsa_circ_210329,RMVar_hsa_circ_210330,RMVar_hsa_circ_332693 67558 RMVar_ID_67558 Human_SNP_ID_682073572 m1A Human chr20 + 44614648 44614648 44614648 GAATGCGGTCCCTGACATCCAGGGAGACTCAGAGGCTGTGAGCGTGAGGAAGCTGGCTGGAGACA GAATGCGGTCCCTGACATCCAGGGAGACTCAGGGGCTGTGAGCGTGAGGAAGCTGGCTGGAGACA A G PKIG Ensembl:ENSG00000168734 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44614600..44614682 26863196 MeRIP-seq:(Medium) rs1309621434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564732,Human_RBP_ID_4660447,Human_RBP_ID_9389345,Human_RBP_ID_17659371 Human_Splice_Rec_2086823,Human_Splice_Rec_2086831,Human_Splice_Rec_2086841,Human_Splice_Rec_2086851,Human_Splice_Rec_2086859,Human_Splice_Rec_2086869,Human_Splice_Rec_2086871 Human_miRNA_ID_2909493 RMVar_hsa_circ_28750,RMVar_hsa_circ_87348,RMVar_hsa_circ_109947,RMVar_hsa_circ_210328,RMVar_hsa_circ_210329,RMVar_hsa_circ_210331,RMVar_hsa_circ_119198 67559 RMVar_ID_67559 Human_SNP_ID_682077495 m1A Human chr20 - 44629148 44629148 44629148 TTTGTTTCCAGGAGGAGAGGGATCGCCCTCCCAGCTAACACAGCAGAGGGGCTGCTGAACGTCAT TTTGTTTCCAGGAGGAGAGGGATCGCCCTCCCGGCTAACACAGCAGAGGGGCTGCTGAACGTCAT T C ADA Ensembl:ENSG00000196839 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:44629100..44636100 32194978 MeRIP-seq:(Medium) rs747148184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26820881 Human_Splice_Rec_2086888,Human_Splice_Rec_2086910,Human_Splice_Rec_2086930,Human_Splice_Rec_2086950,Human_Splice_Rec_2086966,Human_Splice_Rec_2086986,Human_Splice_Rec_2086992 RMVar_hsa_circ_118339,RMVar_hsa_circ_92423,RMVar_hsa_circ_82667,RMVar_hsa_circ_210333,RMVar_hsa_circ_210334,RMVar_hsa_circ_210332,RMVar_hsa_circ_210345,RMVar_hsa_circ_81724,RMVar_hsa_circ_85154,RMVar_hsa_circ_80821,RMVar_hsa_circ_210346,RMVar_hsa_circ_210344,RMVar_hsa_circ_352015 67560 RMVar_ID_67560 Human_SNP_ID_682088130 m1A Human chr20 - 44673071 44673070 44673071 CAGGTGGGGATAACTGAAAAAGAGTGCATAAAAGAACGTTGTCCAAGTTGGCACCAGAGTGGGGG CAGGTGGGGATAACTGAAAAAGAGTGCATAAA_GAACGTTGTCCAAGTTGGCACCAGAGTGGGGG CT C AL139352.1 Ensembl:ENSG00000132832 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44673069..44673211 26863196 MeRIP-seq:(Medium) rs1459333639 Functional Loss DEL dbSNP153 33..33 33 - - - 67561 RMVar_ID_67561 Human_SNP_ID_682098384 m1A Human chr20 + 44715402 44715402 44715402 AAAGCTGGCTCTGCAGGGGACATGAGAGGCACACCGAAGACCCACCTCCTGGCCTTCTCCCTCCT AAAGCTGGCTCTGCAGGGGACATGAGAGGCACCCCGAAGACCCACCTCCTGGCCTTCTCCCTCCT A C CCN5 Ensembl:ENSG00000064205 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:44715351..44715558 26863196 MeRIP-seq:(Medium) rs1294690589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27486155 Human_Splice_Rec_2087034,Human_Splice_Rec_2087035,Human_Splice_Rec_2087041,Human_Splice_Rec_2087045,Human_Splice_Rec_2087047 67562 RMVar_ID_67562 Human_SNP_ID_682098401 m1A Human chr20 - 44715427 44715427 44715427 CCTCCTTACCTTTGAGAGGAGGCAGAGGAGGGAGAAGGCCAGGAGGTGGGTCTTCGGTGTGCCTC CCTCCTTACCTTTGAGAGGAGGCAGAGGAGGGGGAAGGCCAGGAGGTGGGTCTTCGGTGTGCCTC T C KCNK15-AS1 Ensembl:ENSG00000244558 lincRNA intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr20:44715376..44715450;chr20:44715351..44715548 26863196 MeRIP-seq:(Medium) rs775607816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5595837 67563 RMVar_ID_67563 Human_SNP_ID_682099501 m1A Human chr20 - 44719970 44719970 44719970 ATACCCGGCAGCAGCCACAGCCATCCAGCACCAGGGGTACTCCCAGCGGGCATCGGGGAGGTGGC ATACCCGGCAGCAGCCACAGCCATCCAGCACCGGGGGTACTCCCAGCGGGCATCGGGGAGGTGGC T C KCNK15-AS1 Ensembl:ENSG00000244558 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:44719926..44719975 26863196 MeRIP-seq:(Medium) rs992818174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5595842 67564 RMVar_ID_67564 Human_SNP_ID_682101341 m1A Human chr20 - 44727072 44727072 44727072 GGCCAGAAAACTGGGGTCCTAGGGGGGAAAGAACAAGAGTTAGCACTGAGCAGCCAGGGCTCAGC GGCCAGAAAACTGGGGTCCTAGGGGGGAAAGAGCAAGAGTTAGCACTGAGCAGCCAGGGCTCAGC T C KCNK15-AS1 Ensembl:ENSG00000244558 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44727069..44727259 26863196 MeRIP-seq:(Medium) rs1281402210 Functional Loss SNV dbSNP153 33..33 33 - - - 67565 RMVar_ID_67565 Human_SNP_ID_682105802 m1A Human chr20 + 44746013 44746013 44746013 CTGTCTTCGACGCGCTCGAGTCCGAGGCGGAAAGCGGCCGCCAGCGACTGCTGGTCCAGAAGCGG CTGTCTTCGACGCGCTCGAGTCCGAGGCGGAATGCGGCCGCCAGCGACTGCTGGTCCAGAAGCGG A T KCNK15 Ensembl:ENSG00000124249 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:44745963..44746108 26863196 MeRIP-seq:(Medium) rs548589122 Functional Loss SNV dbSNP153 33..33 33 - - - 67566 RMVar_ID_67566 Human_SNP_ID_682121286 m1A Human chr20 + 44810451 44810451 44810451 CTGGCGGGCGCGGCGGGGCCGGCGGGCGGGCCAGGAGCTGGCGGCGCGCGGAGCCCGAGGCGCGC CTGGCGGGCGCGGCGGGGCCGGCGGGCGGGCCCGGAGCTGGCGGCGCGCGGAGCCCGAGGCGCGC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:44810363..44810508 26863410 MeRIP-seq:(Medium) rs1455169307 Functional Loss SNV dbSNP153 33..33 33 - - - 67567 RMVar_ID_67567 Human_SNP_ID_682121314 m1A Human chr20 - 44810516 44810495 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC_____________________GCCAGCAGCACA CGGCGGCGGCGGCGGCGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1243869190 Functional Loss DEL dbSNP153 33..53 33 - - - 67568 RMVar_ID_67568 Human_SNP_ID_682121320 m1A Human chr20 - 44810516 44810498 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC__________________GCCGCCAGCAGCACA CGGCGGCGGCGGCGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1360616056 Functional Loss DEL dbSNP153 33..50 33 - - - 67569 RMVar_ID_67569 Human_SNP_ID_682121327 m1A Human chr20 - 44810516 44810501 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC_______________GCCGCCGCCAGCAGCACA CGGCGGCGGCGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1328897938 Functional Loss DEL dbSNP153 33..47 33 - - - 67570 RMVar_ID_67570 Human_SNP_ID_682121332 m1A Human chr20 - 44810516 44810504 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC____________GCCGCCGCCGCCAGCAGCACA CGGCGGCGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs972584206 Functional Loss DEL dbSNP153 33..44 33 - - - 67571 RMVar_ID_67571 Human_SNP_ID_682121342 m1A Human chr20 - 44810516 44810507 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC_________GCCGCCGCCGCCGCCAGCAGCACA CGGCGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1219214750 Functional Loss DEL dbSNP153 33..41 33 - - - 67572 RMVar_ID_67572 Human_SNP_ID_682121354 m1A Human chr20 - 44810516 44810510 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC______GCCGCCGCCGCCGCCGCCAGCAGCACA CGGCGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1175268053 Functional Loss DEL dbSNP153 33..38 33 - - - 67573 RMVar_ID_67573 Human_SNP_ID_682121364 m1A Human chr20 - 44810516 44810513 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCC___GCCGCCGCCGCCGCCGCCGCCAGCAGCACA CGGT C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs1480861134 Functional Loss DEL dbSNP153 33..35 33 - - - 67574 RMVar_ID_67574 Human_SNP_ID_682121368 m1A Human chr20 - 44810516 44810516 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA T C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs868482057 Functional Loss SNV dbSNP153 33..33 33 - - - 67575 RMVar_ID_67575 Human_SNP_ID_682139040 m1A Human chr20 + 44885780 44885780 44885780 GGGTAGTCGCCGCCGCCGCCGCCGCTGCAGCCACTGCAGGCACCGCTGCCGCCGCCTGAGTAGTG GGGTAGTCGCCGCCGCCGCCGCCGCTGCAGCCCCTGCAGGCACCGCTGCCGCCGCCTGAGTAGTG A C YWHAB Ensembl:ENSG00000166913 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:44885675..44885919;chr20:44885701..44885900;chr20:44885676..44885928;chr20:44885676..44885900;chr20:44885675..44885900 26863196 MeRIP-seq:(Medium) rs890175683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244566,Human_RBP_ID_779195,Human_RBP_ID_4649147,Human_RBP_ID_8857399,Human_RBP_ID_9331544,Human_RBP_ID_22453536,Human_RBP_ID_22533646,Human_RBP_ID_23005210,Human_RBP_ID_27021618 RMVar_hsa_circ_210348,RMVar_hsa_circ_117700 67576 RMVar_ID_67576 Human_SNP_ID_682139041 m1A Human chr20 + 44885780 44885780 44885780 GGGTAGTCGCCGCCGCCGCCGCCGCTGCAGCCACTGCAGGCACCGCTGCCGCCGCCTGAGTAGTG GGGTAGTCGCCGCCGCCGCCGCCGCTGCAGCCGCTGCAGGCACCGCTGCCGCCGCCTGAGTAGTG A G YWHAB Ensembl:ENSG00000166913 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:44885675..44885919;chr20:44885701..44885900;chr20:44885676..44885928;chr20:44885676..44885900;chr20:44885675..44885900 26863196 MeRIP-seq:(Medium) rs890175683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244566,Human_RBP_ID_779195,Human_RBP_ID_4649147,Human_RBP_ID_8857399,Human_RBP_ID_9331544,Human_RBP_ID_22453536,Human_RBP_ID_22533646,Human_RBP_ID_23005210,Human_RBP_ID_27021618 RMVar_hsa_circ_210348,RMVar_hsa_circ_117700 67577 RMVar_ID_67577 Human_SNP_ID_682139057 m1A Human chr20 - 44885816 44885816 44885816 AAGCTCCGAGCGAGATGACCTCTTCCTTCCTAAGCCCACTACTCAGGCGGCGGCAGCGGTGCCTG AAGCTCCGAGCGAGATGACCTCTTCCTTCCTACGCCCACTACTCAGGCGGCGGCAGCGGTGCCTG T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:44885726..44885822 26863410 MeRIP-seq:(Medium) rs1385056734 Functional Loss SNV dbSNP153 33..33 33 - - - 67578 RMVar_ID_67578 Human_SNP_ID_682139059 m1A Human chr20 + 44885826 44885826 44885826 TGCCGCCGCCTGAGTAGTGGGCTTAGGAAGGAAGAGGTCATCTCGCTCGGAGCTTCGCTCGGAAG TGCCGCCGCCTGAGTAGTGGGCTTAGGAAGGAGGAGGTCATCTCGCTCGGAGCTTCGCTCGGAAG A G YWHAB Ensembl:ENSG00000166913 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:44885726..44885900 26863410 MeRIP-seq:(Medium) rs1162124959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831768,Human_RBP_ID_1304254,Human_RBP_ID_1597735,Human_RBP_ID_1930295,Human_RBP_ID_4649147,Human_RBP_ID_7004539,Human_RBP_ID_8855125,Human_RBP_ID_9117429,Human_RBP_ID_9331544,Human_RBP_ID_9389346,Human_RBP_ID_14116504,Human_RBP_ID_18773831,Human_RBP_ID_22453537,Human_RBP_ID_23005210,Human_RBP_ID_23906659,Human_RBP_ID_27021619 Human_Splice_Rec_2087081,Human_Splice_Rec_2087093,Human_Splice_Rec_2087103,Human_Splice_Rec_2087121,Human_Splice_Rec_2087125 Human_miRNA_ID_2066177,Human_miRNA_ID_2704021,Human_miRNA_ID_2935334 RMVar_hsa_circ_210348,RMVar_hsa_circ_117700 67579 RMVar_ID_67579 Human_SNP_ID_682145261 m1A Human chr20 - 44910172 44910172 44910172 CGGGGTGCAGATCGCCCACGTAAAGCGAGGCAAGCGGGTAGCCAGAACCGCTGGCGTTCATGGTG CGGGGTGCAGATCGCCCACGTAAAGCGAGGCAGGCGGGTAGCCAGAACCGCTGGCGTTCATGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44910131..44910207 26863196 MeRIP-seq:(Medium) rs749246192 Functional Loss SNV dbSNP153 33..33 33 - - - 67580 RMVar_ID_67580 Human_SNP_ID_682145334 m1A Human chr20 - 44910338 44910338 44910338 GTCCTTCCCCTCCCGCCCCATCCCCGGGGCTCACCGTCCGCGGGCTGCTGGAAGTTGATGTAGGC GTCCTTCCCCTCCCGCCCCATCCCCGGGGCTCGCCGTCCGCGGGCTGCTGGAAGTTGATGTAGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:44910161..44912784 32194978 MeRIP-seq:(Medium) rs1351097957 Functional Loss SNV dbSNP153 33..33 33 - - - 67581 RMVar_ID_67581 Human_SNP_ID_682148047 m1A Human chr20 + 44921658 44921658 44921658 CGGGCGGCTGCTGTACGCGGGCCGGGCCCAAAAGCGCGTGGAGCGGCAGAATGAACTGAAGCGCA CGGGCGGCTGCTGTACGCGGGCCGGGCCCAAAGGCGCGTGGAGCGGCAGAATGAACTGAAGCGCA A G PABPC1L Ensembl:ENSG00000101104 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:44916784..44921721 32194978 MeRIP-seq:(Medium) rs200466330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925914,Human_RBP_ID_18423135,Human_RBP_ID_19004334,Human_RBP_ID_27820328 Human_Splice_Rec_2087148,Human_Splice_Rec_2087149,Human_Splice_Rec_2087176,Human_Splice_Rec_2087177,Human_Splice_Rec_2087204,Human_Splice_Rec_2087205,Human_Splice_Rec_2087228,Human_Splice_Rec_2087229,Human_Splice_Rec_2087247,Human_Splice_Rec_2087257 Human_miRNA_ID_2360368 RMVar_hsa_circ_47434,RMVar_hsa_circ_42125,RMVar_hsa_circ_338389,RMVar_hsa_circ_343071,RMVar_hsa_circ_303221,RMVar_hsa_circ_351896,RMVar_hsa_circ_331589,RMVar_hsa_circ_210353,RMVar_hsa_circ_23047,RMVar_hsa_circ_33592,RMVar_hsa_circ_210357,RMVar_hsa_circ_35658,RMVar_hsa_circ_210358,RMVar_hsa_circ_301978 67582 RMVar_ID_67582 Human_SNP_ID_682148076 m1A Human chr20 + 44921712 44921712 44921712 ACTGAAGCGCAGGTTTGAGCAGATGAAGCAGGACCGGCTGAGGCGTTACCAGGTGAGGTCAGGCT ACTGAAGCGCAGGTTTGAGCAGATGAAGCAGGGCCGGCTGAGGCGTTACCAGGTGAGGTCAGGCT A G PABPC1L Ensembl:ENSG00000101104 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44921664..44921793 26863196 MeRIP-seq:(Medium) rs758119580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778631,Human_RBP_ID_831428,Human_RBP_ID_925915,Human_RBP_ID_19005901,Human_RBP_ID_19106598,Human_RBP_ID_22743681 Human_Splice_Rec_2087149,Human_Splice_Rec_2087177,Human_Splice_Rec_2087205,Human_Splice_Rec_2087229,Human_Splice_Rec_2087247,Human_Splice_Rec_2087257 RMVar_hsa_circ_47434,RMVar_hsa_circ_42125,RMVar_hsa_circ_338389,RMVar_hsa_circ_343071,RMVar_hsa_circ_303221,RMVar_hsa_circ_351896,RMVar_hsa_circ_331589,RMVar_hsa_circ_210353,RMVar_hsa_circ_23047,RMVar_hsa_circ_33592,RMVar_hsa_circ_210357,RMVar_hsa_circ_35658,RMVar_hsa_circ_210358,RMVar_hsa_circ_301978 67583 RMVar_ID_67583 Human_SNP_ID_682150334 m1A Human chr20 + 44930602 44930602 44930602 GCCACTCTACGTGGCACTGGCCCAGCGCAAAGAGGAGCGGAAGGCCATCTTGACCAACCAGTACA GCCACTCTACGTGGCACTGGCCCAGCGCAAAGTGGAGCGGAAGGCCATCTTGACCAACCAGTACA A T PABPC1L Ensembl:ENSG00000101104 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:44930551..44931586 32194978 MeRIP-seq:(Medium) rs1170700553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9389356,Human_RBP_ID_19005907,Human_RBP_ID_22080684,Human_RBP_ID_23004781,Human_RBP_ID_26343034,Human_RBP_ID_27820330 Human_Splice_Rec_2087208,Human_Splice_Rec_2087232 RMVar_hsa_circ_47434,RMVar_hsa_circ_42125,RMVar_hsa_circ_343071,RMVar_hsa_circ_33592,RMVar_hsa_circ_35658,RMVar_hsa_circ_287291 67584 RMVar_ID_67584 Human_SNP_ID_682155687 m1A Human chr20 - 44951884 44951884 44951884 AGAGGTGGAATTCCTTGCCTTCGGAGAACCACAAAGAGATGGCTAAAAGCAAATCCAAAGAAACC AGAGGTGGAATTCCTTGCCTTCGGAGAACCACGAAGAGATGGCTAAAAGCAAATCCAAAGAAACC T C TOMM34 Ensembl:ENSG00000025772 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44951799..44951932 26863196 MeRIP-seq:(Medium) rs1289891035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2087385 RMVar_hsa_circ_2654,RMVar_hsa_circ_16747 67585 RMVar_ID_67585 Human_SNP_ID_682155902 m1A Human chr20 + 44952883 44952882 44952883 ATGTCTCTGGCTAGGCTGTTTTCCTGGCGGCCAAGCTATTTCAAACCTCTGCTCTCCTCAAACCT ATGTCTCTGGCTAGGCTGTTTTCCTGGCGGCC_AGCTATTTCAAACCTCTGCTCTCCTCAAACCT CA C PABPC1L Ensembl:ENSG00000101104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44952878..44953233 26863196 MeRIP-seq:(Medium) rs1455268653 Functional Loss DEL dbSNP153 33..33 33 - - - 67586 RMVar_ID_67586 Human_SNP_ID_682155903 m1A Human chr20 + 44952883 44952883 44952883 ATGTCTCTGGCTAGGCTGTTTTCCTGGCGGCCAAGCTATTTCAAACCTCTGCTCTCCTCAAACCT ATGTCTCTGGCTAGGCTGTTTTCCTGGCGGCCGAGCTATTTCAAACCTCTGCTCTCCTCAAACCT A G PABPC1L Ensembl:ENSG00000101104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:44952878..44953233 26863196 MeRIP-seq:(Medium) rs1413727523 Functional Loss SNV dbSNP153 33..33 33 - - - 67587 RMVar_ID_67587 Human_SNP_ID_682159314 m1A Human chr20 - 44966546 44966546 44966546 CCGTCTCCATGGCGCTGCCAGCAGCCGCCCAGACCCGCTCACTGCTCCATCCTCCCGCGGACCTC CCGTCTCCATGGCGCTGCCAGCAGCCGCCCAGCCCCGCTCACTGCTCCATCCTCCCGCGGACCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:44966490..44972133 26863196 MeRIP-seq:(Medium) rs1306277337 Functional Loss SNV dbSNP153 33..33 33 - - - 67588 RMVar_ID_67588 Human_SNP_ID_682159316 m1A Human chr20 - 44966548 44966548 44966548 TACCGTCTCCATGGCGCTGCCAGCAGCCGCCCAGACCCGCTCACTGCTCCATCCTCCCGCGGACC TACCGTCTCCATGGCGCTGCCAGCAGCCGCCCGGACCCGCTCACTGCTCCATCCTCCCGCGGACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:44966501..44972150;chr20:44966501..44972133;chr20:44966494..44972133 26863196 MeRIP-seq:(Medium) rs764502815 Functional Loss SNV dbSNP153 33..33 33 - - - 67589 RMVar_ID_67589 Human_SNP_ID_682159327 m1A Human chr20 + 44966575 44966575 44966575 GGGTCTGGGCGGCTGCTGGCAGCGCCATGGAGACGGTACAGCTGAGGAACCCGCCGCGCCGGTGA GGGTCTGGGCGGCTGCTGGCAGCGCCATGGAGGCGGTACAGCTGAGGAACCCGCCGCGCCGGTGA A G STK4 Ensembl:ENSG00000101109 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:44966494..44966620 26863196 MeRIP-seq:(Medium) rs1291531683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244739,Human_RBP_ID_779711,Human_RBP_ID_4659863,Human_RBP_ID_9390825,Human_RBP_ID_18422903,Human_RBP_ID_23004783,Human_RBP_ID_26343036,Human_RBP_ID_27819836 Human_Splice_Rec_2087397,Human_Splice_Rec_2087415,Human_Splice_Rec_2087435,Human_Splice_Rec_2087437,Human_Splice_Rec_2087459,Human_Splice_Rec_2087465 67590 RMVar_ID_67590 Human_SNP_ID_682160645 m1A Human chr20 - 44971984 44971984 44971984 TATATCTTTTTTTTATAATTAGCATCTCAGGAACTTCTCTATACAGACTTCACTAGTTAAGACTG TATATCTTTTTTTTATAATTAGCATCTCAGGATCTTCTCTATACAGACTTCACTAGTTAAGACTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:44971982..44972114 26863196 MeRIP-seq:(Medium) rs1052079596 Functional Loss SNV dbSNP153 33..33 33 - - - 67591 RMVar_ID_67591 Human_SNP_ID_682227051 m1A Human chr20 - 45253633 45253632 45253634 CAGAGTGACTGGCAGTGTCCAGGGAAGAAGAGATGTTGTCCTGACACTTGTGGCATCAAATGCCT CAGAGTGACTGGCAGTGTCCAGGGAAGAAGA__TGTTGTCCTGACACTTGTGGCATCAAATGCCT ATC A SLPI Ensembl:ENSG00000124107 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45253538..45253637 26863196 MeRIP-seq:(Medium) rs748887174 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_2087537 Human_miRNA_ID_2627818,Human_miRNA_ID_2748654 RMVar_hsa_circ_83580,RMVar_hsa_circ_117456,RMVar_hsa_circ_210379,RMVar_hsa_circ_113958,RMVar_hsa_circ_210378,RMVar_hsa_circ_210381 67592 RMVar_ID_67592 Human_SNP_ID_682227306 m1A Human chr20 + 45254509 45254509 45254509 CAGCCCAAGGTGCCAGAGTTCCCAGGGCAAGCAGCACCAGGAAGGGGAAGAGGCCGCTGGACTTC CAGCCCAAGGTGCCAGAGTTCCCAGGGCAAGCGGCACCAGGAAGGGGAAGAGGCCGCTGGACTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45254417..45254510 26863196 MeRIP-seq:(Medium) rs184019207 Functional Loss SNV dbSNP153 33..33 33 - - - 67593 RMVar_ID_67593 Human_SNP_ID_682249009 m1A Human chr20 - 45335873 45335873 45335873 GTCATCGACCCCCAGGACCTCCTAGAAGGCCGATACTTCTCCGGAGCCCTACCAGACGATGAGGA GTCATCGACCCCCAGGACCTCCTAGAAGGCCGGTACTTCTCCGGAGCCCTACCAGACGATGAGGA T C SDC4 Ensembl:ENSG00000124145 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1235982736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1026286,Human_RBP_ID_4660455,Human_RBP_ID_9390832,Human_RBP_ID_17700587,Human_RBP_ID_17972591,Human_RBP_ID_22395242,Human_RBP_ID_22453110 Human_Splice_Rec_2087692,Human_Splice_Rec_2087693 RMVar_hsa_circ_101700,RMVar_hsa_circ_102036,RMVar_hsa_circ_210385,RMVar_hsa_circ_210386,RMVar_hsa_circ_23306,RMVar_hsa_circ_43872,RMVar_hsa_circ_113437,RMVar_hsa_circ_312721,RMVar_hsa_circ_210389 67594 RMVar_ID_67594 Human_SNP_ID_682251970 m1A Human chr20 + 45348245 45348244 45348246 GGGGGTAGCGTACCCCCGATCTGCCCCCCCCCATCCCACGCTCCGACGAACAAAGGAGGCACCGG GGGGGTAGCGTACCCCCGATCTGCCCCCCCCC__CCCACGCTCCGACGAACAAAGGAGGCACCGG CAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45348239..45348344 26863196 MeRIP-seq:(Medium) rs1491441392 Functional Loss DEL dbSNP153 33..34 33 - - - 67595 RMVar_ID_67595 Human_SNP_ID_682251971 m1A Human chr20 + 45348245 45348244 45348245 GGGGGTAGCGTACCCCCGATCTGCCCCCCCCCATCCCACGCTCCGACGAACAAAGGAGGCACCGG GGGGGTAGCGTACCCCCGATCTGCCCCCCCCC_TCCCACGCTCCGACGAACAAAGGAGGCACCGG CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45348239..45348344 26863196 MeRIP-seq:(Medium) rs1568910771 Functional Loss DEL dbSNP153 33..33 33 - - - 67596 RMVar_ID_67596 Human_SNP_ID_682251972 m1A Human chr20 + 45348245 45348245 45348245 GGGGGTAGCGTACCCCCGATCTGCCCCCCCCCATCCCACGCTCCGACGAACAAAGGAGGCACCGG GGGGGTAGCGTACCCCCGATCTGCCCCCCCCCCTCCCACGCTCCGACGAACAAAGGAGGCACCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45348239..45348344 26863196 MeRIP-seq:(Medium) rs1420175278 Functional Loss SNV dbSNP153 33..33 33 - - - 67597 RMVar_ID_67597 Human_SNP_ID_682255435 m1A Human chr20 + 45363245 45363245 45363245 GGCAGCGCCTCTCCTCCATGGTCCTGTCTGTCAGCGCTGTTTTGGGAGCCCGCCGGTGAGGCCGG GGCAGCGCCTCTCCTCCATGGTCCTGTCTGTCCGCGCTGTTTTGGGAGCCCGCCGGTGAGGCCGG A C SYS1,SYS1-DBNDD2 Ensembl:ENSG00000204070,Ensembl:ENSG00000254806 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45363195..45363334 26863196 MeRIP-seq:(Medium) rs1022440377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63735,Human_RBP_ID_4659428,Human_RBP_ID_5423771,Human_RBP_ID_5445656,Human_RBP_ID_27486254 Human_Splice_Rec_2087700,Human_Splice_Rec_2087701,Human_Splice_Rec_2087708,Human_Splice_Rec_2087709,Human_Splice_Rec_2087715,Human_Splice_Rec_2087721,Human_Splice_Rec_2087725,Human_Splice_Rec_2087731,Human_Splice_Rec_2087743,Human_Splice_Rec_2087753 67598 RMVar_ID_67598 Human_SNP_ID_682256449 m1A Human chr20 + 45367094 45367094 45367094 CGGACGGAGCTCAAGGAGATACCCCTCAACTCAGCCCCTAAATCCAATGTCTAGAATCAGGCCCT CGGACGGAGCTCAAGGAGATACCCCTCAACTCGGCCCCTAAATCCAATGTCTAGAATCAGGCCCT A G SYS1,SYS1-DBNDD2 Ensembl:ENSG00000204070,Ensembl:ENSG00000254806 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45367045..45368140 32194978 MeRIP-seq:(Medium) rs752443252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27486261 RMVar_hsa_circ_210390 67599 RMVar_ID_67599 Human_SNP_ID_682265432 m1A Human chr20 + 45406365 45406365 45406365 CGCCGCGGGTCTGCGCGGGGCGGGGGCGCAGCAAGTGCATCCGAGCGAGCGGAGACTAGCGCACC CGCCGCGGGTCTGCGCGGGGCGGGGGCGCAGCGAGTGCATCCGAGCGAGCGGAGACTAGCGCACC A G SYS1-DBNDD2,DBNDD2 Ensembl:ENSG00000254806,Ensembl:ENSG00000244274 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45406363..45406446 26863196 MeRIP-seq:(Medium) rs1329838028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7005611 RMVar_hsa_circ_210390 67600 RMVar_ID_67600 Human_SNP_ID_682266014 m1A Human chr20 - 45408417 45408417 45408417 AGGAGCAAAACAAGTACAGCTGCAAAGTCGAAAGAGAAGACAGAGGGGACCTGGGCTTGGGGCGC AGGAGCAAAACAAGTACAGCTGCAAAGTCGAAGGAGAAGACAGAGGGGACCTGGGCTTGGGGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45408414..45408630 26863196 MeRIP-seq:(Medium) rs746116467 Functional Loss SNV dbSNP153 33..33 33 - - - 67601 RMVar_ID_67601 Human_SNP_ID_682266015 m1A Human chr20 - 45408417 45408417 45408417 AGGAGCAAAACAAGTACAGCTGCAAAGTCGAAAGAGAAGACAGAGGGGACCTGGGCTTGGGGCGC AGGAGCAAAACAAGTACAGCTGCAAAGTCGAACGAGAAGACAGAGGGGACCTGGGCTTGGGGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45408414..45408630 26863196 MeRIP-seq:(Medium) rs746116467 Functional Loss SNV dbSNP153 33..33 33 - - - 67602 RMVar_ID_67602 Human_SNP_ID_682266525 m1A Human chr20 - 45410144 45410144 45410144 AGCCAGCGTGGTCAGTCTGTAGGCAGGGGCCCACTGCTAGCTGCAGGCTCCAGGCTCTGCCCCTC AGCCAGCGTGGTCAGTCTGTAGGCAGGGGCCCGCTGCTAGCTGCAGGCTCCAGGCTCTGCCCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45410095..45410213 26863196 MeRIP-seq:(Medium) rs1223183512 Functional Loss SNV dbSNP153 33..33 33 - - - 67603 RMVar_ID_67603 Human_SNP_ID_682268681 m1A Human chr20 - 45418942 45418942 45418942 GCCAGACCCAGGGGTTTGAAGGAGGCAGTGGGAGTGACTGTGTTGGTGGAGTCGATGAAGTTGAG GCCAGACCCAGGGGTTTGAAGGAGGCAGTGGGGGTGACTGTGTTGGTGGAGTCGATGAAGTTGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45418892..45419017 26863196 MeRIP-seq:(Medium) rs1374718381 Functional Loss SNV dbSNP153 33..33 33 - - - 67604 RMVar_ID_67604 Human_SNP_ID_682270887 m1A Human chr20 + 45425651 45425651 45425651 GGAGCCGCTGCTGGTGAACCTGCCGACACCGGACTTCAGCATGCCCTACAACGTGATCTGCCTCA GGAGCCGCTGCTGGTGAACCTGCCGACACCGGCCTTCAGCATGCCCTACAACGTGATCTGCCTCA A C PIGT Ensembl:ENSG00000124155 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45425600..45425841 26863196 MeRIP-seq:(Medium) rs1316149186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565125,Human_RBP_ID_1930494,Human_RBP_ID_8534349,Human_RBP_ID_14119658,Human_RBP_ID_17396609,Human_RBP_ID_18774050,Human_RBP_ID_27486309 Human_Splice_Rec_2087874,Human_Splice_Rec_2087894,Human_Splice_Rec_2087914,Human_Splice_Rec_2087936,Human_Splice_Rec_2087958,Human_Splice_Rec_2087978,Human_Splice_Rec_2087998,Human_Splice_Rec_2088042,Human_Splice_Rec_2088064,Human_Splice_Rec_2088086,Human_Splice_Rec_2088136,Human_Splice_Rec_2088172,Human_Splice_Rec_2088192,Human_Splice_Rec_2088212,Human_Splice_Rec_2088234,Human_Splice_Rec_2088254,Human_Splice_Rec_2088276,Human_Splice_Rec_2088298,Human_Splice_Rec_2088320,Human_Splice_Rec_2088342,Human_Splice_Rec_2088362,Human_Splice_Rec_2088384,Human_Splice_Rec_2088406,Human_Splice_Rec_2088428,Human_Splice_Rec_2088522,Human_Splice_Rec_2088554,Human_Splice_Rec_2088612,Human_Splice_Rec_2088670,Human_Splice_Rec_2088704,Human_Splice_Rec_2088724,Human_Splice_Rec_2088750,Human_Splice_Rec_2088768,Human_Splice_Rec_2088788,Human_Splice_Rec_2088822,Human_Splice_Rec_2088842,Human_Splice_Rec_2088860,Human_Splice_Rec_2088880,Human_Splice_Rec_2088912,Human_Splice_Rec_2088948,Human_Splice_Rec_2088950,Human_Splice_Rec_2088954,Human_Splice_Rec_2088968 RMVar_hsa_circ_53277,RMVar_hsa_circ_362648 67605 RMVar_ID_67605 Human_SNP_ID_682321190 m1A Human chr20 - 45641233 45641233 45641233 CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCAAGGCCGCGGAGCTCGCGAAGGCAAGCCCGAGGA CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCACGGCCGCGGAGCTCGCGAAGGCAAGCCCGAGGA T G RPS2P7 Ensembl:ENSG00000235508 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45641190..45641335 26863196 MeRIP-seq:(Medium) rs1352520702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1841216 67606 RMVar_ID_67606 Human_SNP_ID_682321238 m1A Human chr20 - 45641310 45641310 45641310 GGCCCGGAGGCCCTGGTGGCCCTGGGATGGGGAACCGCGGTGGCTTCCGCGGAGGTTTCGGCAGT GGCCCGGAGGCCCTGGTGGCCCTGGGATGGGGGACCGCGGTGGCTTCCGCGGAGGTTTCGGCAGT T C RPS2P7 Ensembl:ENSG00000235508 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:45641222..45641350 26863410 MeRIP-seq:(Medium) rs1404854751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17673678,Human_RBP_ID_21960284 Human_miRNA_ID_1896453,Human_miRNA_ID_1903603 67607 RMVar_ID_67607 Human_SNP_ID_682321252 m1A Human chr20 - 45641343 45641343 45641343 ACCAAATGGCGGATGACGCCGGTGCAGCGGGGAGGCCCGGAGGCCCTGGTGGCCCTGGGATGGGG ACCAAATGGCGGATGACGCCGGTGCAGCGGGGGGGCCCGGAGGCCCTGGTGGCCCTGGGATGGGG T C RPS2P7 Ensembl:ENSG00000235508 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs2425731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8260806,Human_RBP_ID_17673678,Human_RBP_ID_21960284 Human_miRNA_ID_1870161 GWAS_ID_8034,GWAS_ID_8035,GWAS_ID_8036,GWAS_ID_8037,GWAS_ID_8038,GWAS_ID_8039,GWAS_ID_8040,GWAS_ID_8041,GWAS_ID_8042,GWAS_ID_8043,GWAS_ID_8044,GWAS_ID_8045,GWAS_ID_8046,GWAS_ID_8047,GWAS_ID_8048,GWAS_ID_8049,GWAS_ID_8050,GWAS_ID_8051,GWAS_ID_8052,GWAS_ID_8053,GWAS_ID_8054,GWAS_ID_8055,GWAS_ID_8056,GWAS_ID_8057,GWAS_ID_8058,GWAS_ID_8059,GWAS_ID_8060,GWAS_ID_8061,GWAS_ID_8062,GWAS_ID_8063,GWAS_ID_8064,GWAS_ID_8065,GWAS_ID_8066,GWAS_ID_8067,GWAS_ID_8068,GWAS_ID_8069,GWAS_ID_8070,GWAS_ID_8071,GWAS_ID_8072,GWAS_ID_8073,GWAS_ID_8074,GWAS_ID_8075,GWAS_ID_8076,GWAS_ID_8077,GWAS_ID_8078,GWAS_ID_8079,GWAS_ID_8080,GWAS_ID_8081,GWAS_ID_8082,GWAS_ID_8083,GWAS_ID_8084,GWAS_ID_8085,GWAS_ID_8086,GWAS_ID_8087,GWAS_ID_8088,GWAS_ID_8089,GWAS_ID_8090,GWAS_ID_8091,GWAS_ID_8092,GWAS_ID_8093,GWAS_ID_8094 67608 RMVar_ID_67608 Human_SNP_ID_682360051 m1A Human chr20 + 45792014 45792014 45792014 GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCACTGGCGACGCCGAGCAGCCGCGGGGACCTAGC GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCGCTGGCGACGCCGAGCAGCCGCGGGGACCTAGC A G DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45791951..45792143 26863196 MeRIP-seq:(Medium) rs753122969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244662,Human_RBP_ID_4659436 Human_Splice_Rec_2089223,Human_Splice_Rec_2089247,Human_Splice_Rec_2089255 67609 RMVar_ID_67609 Human_SNP_ID_682360052 m1A Human chr20 + 45792014 45792014 45792014 GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCACTGGCGACGCCGAGCAGCCGCGGGGACCTAGC GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCTCTGGCGACGCCGAGCAGCCGCGGGGACCTAGC A T DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45791951..45792143 26863196 MeRIP-seq:(Medium) rs753122969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244662,Human_RBP_ID_4659436 Human_Splice_Rec_2089223,Human_Splice_Rec_2089247,Human_Splice_Rec_2089255 67610 RMVar_ID_67610 Human_SNP_ID_682360222 m1A Human chr20 + 45792633 45792631 45792633 TTCATACCCACCCTCCACCTCCACCCCACCCCAGTGTCACAGGCCGCAGTGACATTTGTTCCGTT TTCATACCCACCCTCCACCTCCACCCCACCC__GTGTCACAGGCCGCAGTGACATTTGTTCCGTT CCA C DNTTIP1 Ensembl:ENSG00000101457 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45792630..45792787 26863196 MeRIP-seq:(Medium) rs1050757698 Functional Loss DEL dbSNP153 32..33 33 - - - 67611 RMVar_ID_67611 Human_SNP_ID_682360239 m1A Human chr20 + 45792678 45792678 45792678 GCAGTGACATTTGTTCCGTTGGTCCCCACAGAACCCTTGGAACATAATGATAAAGCACCGGCAGG GCAGTGACATTTGTTCCGTTGGTCCCCACAGACCCCTTGGAACATAATGATAAAGCACCGGCAGG A C DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45792676..45792750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2089224,Human_Splice_Rec_2089225,Human_Splice_Rec_2089248,Human_Splice_Rec_2089249,Human_Splice_Rec_2089256,Human_Splice_Rec_2089257,Human_Splice_Rec_2089277 RMVar_hsa_circ_63398 67612 RMVar_ID_67612 Human_SNP_ID_682360240 m1A Human chr20 + 45792678 45792678 45792678 GCAGTGACATTTGTTCCGTTGGTCCCCACAGAACCCTTGGAACATAATGATAAAGCACCGGCAGG GCAGTGACATTTGTTCCGTTGGTCCCCACAGAGCCCTTGGAACATAATGATAAAGCACCGGCAGG A G DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45792676..45792750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2089224,Human_Splice_Rec_2089225,Human_Splice_Rec_2089248,Human_Splice_Rec_2089249,Human_Splice_Rec_2089256,Human_Splice_Rec_2089257,Human_Splice_Rec_2089277 RMVar_hsa_circ_63398 67613 RMVar_ID_67613 Human_SNP_ID_682360243 m1A Human chr20 - 45792682 45792681 45792682 TGCACCTGCCGGTGCTTTATCATTATGTTCCAAGGGTTCTGTGGGGACCAACGGAACAAATGTCA TGCACCTGCCGGTGCTTTATCATTATGTTCCA_GGGTTCTGTGGGGACCAACGGAACAAATGTCA CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:45792676..45792750 26863196 MeRIP-seq:(Medium) rs1568703924 Functional Loss DEL dbSNP153 33..33 33 - - - 67614 RMVar_ID_67614 Human_SNP_ID_682360244 m1A Human chr20 - 45792682 45792682 45792682 TGCACCTGCCGGTGCTTTATCATTATGTTCCAAGGGTTCTGTGGGGACCAACGGAACAAATGTCA TGCACCTGCCGGTGCTTTATCATTATGTTCCAGGGGTTCTGTGGGGACCAACGGAACAAATGTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:45792676..45792750 26863196 MeRIP-seq:(Medium) rs903681425 Functional Loss SNV dbSNP153 33..33 33 - - - 67615 RMVar_ID_67615 Human_SNP_ID_682360537 m1A Human chr20 + 45793871 45793871 45793871 CTATGTCCATAATTAACTGGGGAGGCTGGGAAAGAATATGTTTGGGACATGCCCCCTCACCCTGT CTATGTCCATAATTAACTGGGGAGGCTGGGAACGAATATGTTTGGGACATGCCCCCTCACCCTGT A C DNTTIP1 Ensembl:ENSG00000101457 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45793869..45794000 26863196 MeRIP-seq:(Medium) rs577364629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63398 67616 RMVar_ID_67616 Human_SNP_ID_682360548 m1A Human chr20 - 45793903 45793903 45793903 GCAGGATCTGTGAAACTGCATTCAGGAGGGAGACAGGGTGAGGGGGCATGTCCCAAACATATTCT GCAGGATCTGTGAAACTGCATTCAGGAGGGAGGCAGGGTGAGGGGGCATGTCCCAAACATATTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45793901..45794000 26863196 MeRIP-seq:(Medium) rs758609028 Functional Loss SNV dbSNP153 33..33 33 - - - 67617 RMVar_ID_67617 Human_SNP_ID_682362825 m1A Human chr20 - 45802016 45802016 45802016 GCGGCTGCCCGGTCGCTTGACAGGATGTGTCCAGGAGGCCGTCCTTTCCTCTGCCACAAAAAACA GCGGCTGCCCGGTCGCTTGACAGGATGTGTCCGGGAGGCCGTCCTTTCCTCTGCCACAAAAAACA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45801427..45803056 32194978 MeRIP-seq:(Medium) rs1465122438 Functional Loss SNV dbSNP153 33..33 33 - - - 67618 RMVar_ID_67618 Human_SNP_ID_682364922 m1A Human chr20 + 45811164 45811164 45811164 GTATATGGAGACACTACGGACAGAGAATGAGCATCGTGCTGTTGAAGCACCTCCACAGACCTGAG GTATATGGAGACACTACGGACAGAGAATGAGCTTCGTGCTGTTGAAGCACCTCCACAGACCTGAG A T DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45811116..45811247 26863196 MeRIP-seq:(Medium) rs745762179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9331546,Human_RBP_ID_9389381,Human_RBP_ID_14120023,Human_RBP_ID_17659391,Human_RBP_ID_20661154 Human_miRNA_ID_2587803 RMVar_hsa_circ_96664,RMVar_hsa_circ_210395 67619 RMVar_ID_67619 Human_SNP_ID_682365664 m1A Human chr20 - 45813428 45813427 45813429 AGGGTCATCAGCTCCTGCTGTAGCCTGAAAAAAGAGTATTCGGGGTTACCTGGGAGTCTGGATGG AGGGTCATCAGCTCCTGCTGTAGCCTGAAAA__GAGTATTCGGGGTTACCTGGGAGTCTGGATGG CTT C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:45813426..45813475 26863196 MeRIP-seq:(Medium) rs751180069 Functional Loss DEL dbSNP153 32..33 33 - - - 67620 RMVar_ID_67620 Human_SNP_ID_682365666 m1A Human chr20 - 45813428 45813428 45813428 AGGGTCATCAGCTCCTGCTGTAGCCTGAAAAAAGAGTATTCGGGGTTACCTGGGAGTCTGGATGG AGGGTCATCAGCTCCTGCTGTAGCCTGAAAAAGGAGTATTCGGGGTTACCTGGGAGTCTGGATGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:45813426..45813475 26863196 MeRIP-seq:(Medium) rs775782250 Functional Loss SNV dbSNP153 33..33 33 - - - 67621 RMVar_ID_67621 Human_SNP_ID_682366115 m1A Human chr20 + 45814470 45814470 45814470 TGGGTAGGGACCATCCATGGAGCAGCTGGAACAGTAAGTGTAGGGCTGGGATGGGTGAGTGAGTC TGGGTAGGGACCATCCATGGAGCAGCTGGAACCGTAAGTGTAGGGCTGGGATGGGTGAGTGAGTC A C UBE2C Ensembl:ENSG00000175063 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45814376..45814475 32194978 MeRIP-seq:(Medium) rs1251220053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5385262,Human_RBP_ID_7005815,Human_RBP_ID_14120141,Human_RBP_ID_17972696 Human_Splice_Rec_2089312,Human_Splice_Rec_2089313,Human_Splice_Rec_2089328,Human_Splice_Rec_2089329,Human_Splice_Rec_2089338,Human_Splice_Rec_2089339,Human_Splice_Rec_2089362,Human_Splice_Rec_2089363,Human_Splice_Rec_2089369 RMVar_hsa_circ_89472,RMVar_hsa_circ_123205,RMVar_hsa_circ_210396,RMVar_hsa_circ_210397 67622 RMVar_ID_67622 Human_SNP_ID_682366477 m1A Human chr20 - 45815600 45815600 45815600 TAGCAGGGCGTGAGGAACTTCACTGTGGGCGCATTGTAAGGGTAGCCACTGGGGAACTCTAGCGA TAGCAGGGCGTGAGGAACTTCACTGTGGGCGCGTTGTAAGGGTAGCCACTGGGGAACTCTAGCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45815507..45815648 26863196 MeRIP-seq:(Medium) rs141555061 Functional Loss SNV dbSNP153 33..33 33 - - - 67623 RMVar_ID_67623 Human_SNP_ID_682366489 m1A Human chr20 - 45815628 45815626 45815629 GTTACCCTGGGTGTCCACGTTGGGGTGATAGCAGGGCGTGAGGAACTTCACTGTGGGCGCATTGT GTTACCCTGGGTGTCCACGTTGGGGTGATAG___GGCGTGAGGAACTTCACTGTGGGCGCATTGT CCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45815577..45815943 26863196 MeRIP-seq:(Medium) rs773543281 Functional Loss DEL dbSNP153 32..34 33 - - - 67624 RMVar_ID_67624 Human_SNP_ID_682374403 m1A Human chr20 - 45844378 45844378 45844378 CTCCAAAAGAGGTACCCATTGGCGCTCAACCGAATTGCTGCTCAGGAGGTCCCCATTGAGATCAA CTCCAAAAGAGGTACCCATTGGCGCTCAACCGCATTGCTGCTCAGGAGGTCCCCATTGAGATCAA T G ACOT8 Ensembl:ENSG00000101473 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45844330..45844436 26863196 MeRIP-seq:(Medium) rs1429863271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9117542 Human_Splice_Rec_2089454,Human_Splice_Rec_2089464,Human_Splice_Rec_2089474,Human_Splice_Rec_2089482,Human_Splice_Rec_2089490,Human_Splice_Rec_2089494,Human_Splice_Rec_2089498,Human_Splice_Rec_2089500,Human_Splice_Rec_2089510,Human_Splice_Rec_2089518 RMVar_hsa_circ_3272,RMVar_hsa_circ_326991,RMVar_hsa_circ_313865,RMVar_hsa_circ_13376 67625 RMVar_ID_67625 Human_SNP_ID_682387110 m1A Human chr20 - 45891557 45891557 45891557 CGGCGGCGCGGCTCGGATCATCTACGGGAGGCAGCAGAGGGGCTGTTGACTCGCTCCTCAGCGCT CGGCGGCGCGGCTCGGATCATCTACGGGAGGCGGCAGAGGGGCTGTTGACTCGCTCCTCAGCGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:45891551..45891708 26863196 MeRIP-seq:(Medium) rs1276870006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5264036,Human_RBP_ID_7025554,Human_RBP_ID_8112620,Human_RBP_ID_17019214,Human_RBP_ID_17700600,Human_RBP_ID_17977221,Human_RBP_ID_18322851,Human_RBP_ID_18444481,Human_RBP_ID_22506733,Human_RBP_ID_23284003 67626 RMVar_ID_67626 Human_SNP_ID_682387264 m1A Human chr20 + 45891833 45891833 45891833 GATGACGGATGAGGGATGGGGGGTAGTTCTGCAGACCCCTGAGGATGCCTGGGAGCCGGGAGGGC GATGACGGATGAGGGATGGGGGGTAGTTCTGCGGACCCCTGAGGATGCCTGGGAGCCGGGAGGGC A G CTSA Ensembl:ENSG00000064601 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45891830..45891980 32194978 MeRIP-seq:(Medium) rs1323032807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9828,Human_RBP_ID_925942,Human_RBP_ID_5383845,Human_RBP_ID_9431619,Human_RBP_ID_19106630,Human_RBP_ID_22671491,Human_RBP_ID_26342479 RMVar_hsa_circ_14707 67627 RMVar_ID_67627 Human_SNP_ID_682387674 m1A Human chr20 - 45893206 45893206 45893206 CATTGCCCACAGCCAGCCCCTGTGAAACACCCAGGGTGCTCAGCTCATGTGGAGGGCAAAAAGGA CATTGCCCACAGCCAGCCCCTGTGAAACACCCGGGGTGCTCAGCTCATGTGGAGGGCAAAAAGGA T C AL008726.1 Ensembl:ENSG00000271984 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45893201..45894062 32194978 MeRIP-seq:(Medium) rs1315456238 Functional Loss SNV dbSNP153 33..33 33 - - - 67628 RMVar_ID_67628 Human_SNP_ID_682388246 m1A Human chr20 + 45895088 45895088 45895088 TTCCACCTACCTCAACAACCCGTACGTGCGGAAGGCCCTCAACATCCCGGAGCAGCTGCCACAAT TTCCACCTACCTCAACAACCCGTACGTGCGGATGGCCCTCAACATCCCGGAGCAGCTGCCACAAT A T CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45895037..45895162 26863196 MeRIP-seq:(Medium) rs780430995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831101 Human_Splice_Rec_2089564,Human_Splice_Rec_2089565,Human_Splice_Rec_2089592,Human_Splice_Rec_2089593,Human_Splice_Rec_2089626,Human_Splice_Rec_2089627,Human_Splice_Rec_2089666,Human_Splice_Rec_2089667,Human_Splice_Rec_2089694,Human_Splice_Rec_2089695,Human_Splice_Rec_2089736,Human_Splice_Rec_2089737,Human_Splice_Rec_2089764,Human_Splice_Rec_2089772,Human_Splice_Rec_2089773,Human_Splice_Rec_2089782 RMVar_hsa_circ_14707,RMVar_hsa_circ_296311,RMVar_hsa_circ_19067,RMVar_hsa_circ_210408,RMVar_hsa_circ_11833,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000,RMVar_hsa_circ_64193 67629 RMVar_ID_67629 Human_SNP_ID_682388266 m1A Human chr20 + 45895126 45895126 45895126 TCAACATCCCGGAGCAGCTGCCACAATGGGACATGTGCAAGTGAGGTTCCGTGGCCACCTGTGAC TCAACATCCCGGAGCAGCTGCCACAATGGGACGTGTGCAAGTGAGGTTCCGTGGCCACCTGTGAC A G CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45895076..45895125 32194978 MeRIP-seq:(Medium) rs752703552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19108626 Human_Splice_Rec_2089565,Human_Splice_Rec_2089593,Human_Splice_Rec_2089627,Human_Splice_Rec_2089667,Human_Splice_Rec_2089695,Human_Splice_Rec_2089737,Human_Splice_Rec_2089773 RMVar_hsa_circ_14707,RMVar_hsa_circ_296311,RMVar_hsa_circ_19067,RMVar_hsa_circ_210408,RMVar_hsa_circ_11833,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000,RMVar_hsa_circ_64193 67630 RMVar_ID_67630 Human_SNP_ID_682389020 m1A Human chr20 - 45897870 45897870 45897870 GGCCAGAGCCAGGCAGCCAGCTGGCCACTCCCAGGCATACCCGCTCCCAATCCTCCACAGCAGCC GGCCAGAGCCAGGCAGCCAGCTGGCCACTCCCGGGCATACCCGCTCCCAATCCTCCACAGCAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45897867..45897968 32194978 MeRIP-seq:(Medium) rs1448881577 Functional Loss SNV dbSNP153 33..33 33 - - - 67631 RMVar_ID_67631 Human_SNP_ID_682389101 m1A Human chr20 + 45898107 45898107 45898107 AGGAGTTCTCCCACATCGCCTTTCTCACGATCAAGGTAGGGACTGGGCCTGCTGAGAGATAACTG AGGAGTTCTCCCACATCGCCTTTCTCACGATCGAGGTAGGGACTGGGCCTGCTGAGAGATAACTG A G CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45898056..45898121 26863196 MeRIP-seq:(Medium) rs137854549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17659398,Human_RBP_ID_22453128 Human_Splice_Rec_2089571,Human_Splice_Rec_2089599,Human_Splice_Rec_2089633,Human_Splice_Rec_2089673,Human_Splice_Rec_2089701,Human_Splice_Rec_2089743,Human_Splice_Rec_2089783,Human_Splice_Rec_2089789 Clinvar_Rec_273 GWAS_ID_8095 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011 67632 RMVar_ID_67632 Human_SNP_ID_682389234 m1A Human chr20 - 45898489 45898489 45898489 AGAAGAGGACTCTCCTAGCGGGAGAGGCTGGGAGGGGCTGCATCAGGCCGTGGAGCTGGTTGCTG AGAAGAGGACTCTCCTAGCGGGAGAGGCTGGGGGGGGCTGCATCAGGCCGTGGAGCTGGTTGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:45898440..45898556 26863196 MeRIP-seq:(Medium) rs754747052 Functional Loss SNV dbSNP153 33..33 33 - - - 67633 RMVar_ID_67633 Human_SNP_ID_682389249 m1A Human chr20 + 45898526 45898526 45898526 GCCTCTCCCGCTAGGAGAGTCCTCTTCTAAGCAAAGTGCCCCTGCAGGCCGGGTTCTGCCGCCAG GCCTCTCCCGCTAGGAGAGTCCTCTTCTAAGCGAAGTGCCCCTGCAGGCCGGGTTCTGCCGCCAG A G CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45898066..45898770 32194978 MeRIP-seq:(Medium) rs1200625272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565239,Human_RBP_ID_5118990,Human_RBP_ID_5148200,Human_RBP_ID_17659068,Human_RBP_ID_18167702,Human_RBP_ID_18181123 67634 RMVar_ID_67634 Human_SNP_ID_682389280 m1A Human chr20 + 45898650 45898649 45898650 AGCCTGGGGGCAAGTTAGCACTTTATTCCCGCAGCAGTTCCTGAATGGGGTGGCCTGGCCCCTTC AGCCTGGGGGCAAGTTAGCACTTTATTCCCGC_GCAGTTCCTGAATGGGGTGGCCTGGCCCCTTC CA C CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45898601..45898721 32194978 MeRIP-seq:(Medium) rs964386673 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_565243,Human_RBP_ID_779548,Human_RBP_ID_5118991,Human_RBP_ID_5148452,Human_RBP_ID_8204589,Human_RBP_ID_17659069,Human_RBP_ID_18167871,Human_RBP_ID_26493626,Human_RBP_ID_27486397 67635 RMVar_ID_67635 Human_SNP_ID_682389324 m1A Human chr20 + 45898851 45898851 45898851 AATCCCGTCTTCTCTGTGGCACTGGGGGTTAGAGGGGGCACTACAGGCTATGAATGTGGGAAAAG AATCCCGTCTTCTCTGTGGCACTGGGGGTTAGGGGGGGCACTACAGGCTATGAATGTGGGAAAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45898801..45899019 26863196 MeRIP-seq:(Medium) rs906896313 Functional Loss SNV dbSNP153 33..33 33 - - - 67636 RMVar_ID_67636 Human_SNP_ID_682391883 m1A Human chr20 - 45907828 45907828 45907828 GCTTCCTCCTCAACCAGCAGGTGTGGGCAGCGACAGGTCGCAGGGTGGCAAGGGTGGGCATGCTC GCTTCCTCCTCAACCAGCAGGTGTGGGCAGCGGCAGGTCGCAGGGTGGCAAGGGTGGGCATGCTC T C PLTP Ensembl:ENSG00000100979 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45907826..45907875 32194978 MeRIP-seq:(Medium) rs373296330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2089800,Human_Splice_Rec_2089830,Human_Splice_Rec_2089856,Human_Splice_Rec_2089884,Human_Splice_Rec_2089910 RMVar_hsa_circ_210412,RMVar_hsa_circ_304367,RMVar_hsa_circ_337645 67637 RMVar_ID_67637 Human_SNP_ID_682392487 m1A Human chr20 + 45910042 45910042 45910042 CTCCTGCTGTGGCTGGAAATCGAGCTCGGAAGATGTCAGTTGCAGCTCTGTGACCTTCACCCTAC CTCCTGCTGTGGCTGGAAATCGAGCTCGGAAGGTGTCAGTTGCAGCTCTGTGACCTTCACCCTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45909991..45910116 26863196 MeRIP-seq:(Medium) rs1018152670 Functional Loss SNV dbSNP153 33..33 33 - - - 67638 RMVar_ID_67638 Human_SNP_ID_682392921 m1A Human chr20 + 45911443 45911443 45911443 GCCTGCCAGCAGCGCTAGGAAGAGGGCCCCGAAGAGGGCCATGGCGAGCGGGCCTGGGGGTGGGG GCCTGCCAGCAGCGCTAGGAAGAGGGCCCCGAGGAGGGCCATGGCGAGCGGGCCTGGGGGTGGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:45911376..45911491 26863410 MeRIP-seq:(Medium) rs781003189 Functional Loss SNV dbSNP153 33..33 33 - - - 67639 RMVar_ID_67639 Human_SNP_ID_682399055 m1A Human chr20 + 45934774 45934774 45934774 GGCGGCAAAACGGGCGGTCGAGCAGAACGTGTAGCCGCGTCCCCTCCAGTCCGCTCCGGGCAGGT GGCGGCAAAACGGGCGGTCGAGCAGAACGTGTGGCCGCGTCCCCTCCAGTCCGCTCCGGGCAGGT A G PCIF1 Ensembl:ENSG00000100982 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:45934726..45937538 26863196 MeRIP-seq:(Medium) rs1466146594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925947,Human_RBP_ID_4649923 Human_Splice_Rec_2089931,Human_Splice_Rec_2089963 67640 RMVar_ID_67640 Human_SNP_ID_682399116 m1A Human chr20 - 45934918 45934918 45934918 CGCGGGTCTAAGATGGCGGCGGCAACAGAGACAGGGCAAGCGGCAGTCCCGAGCAGAAAGCGCCG CGCGGGTCTAAGATGGCGGCGGCAACAGAGACGGGGCAAGCGGCAGTCCCGAGCAGAAAGCGCCG T C AL162458.1 Ensembl:ENSG00000285796 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45934910..45935040 26863196 MeRIP-seq:(Medium) rs1189995360 Functional Loss SNV dbSNP153 33..33 33 - - - 67641 RMVar_ID_67641 Human_SNP_ID_682407093 m1A Human chr20 - 45959172 45959172 45959172 TGAGGTAAGGTCGGGGCATGGGTCAGGATGACAGAGTGAGGCCGCTTCTCCCAGCCCCAGCATCA TGAGGTAAGGTCGGGGCATGGGTCAGGATGACGGAGTGAGGCCGCTTCTCCCAGCCCCAGCATCA T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:45959170..45959256 26863196 MeRIP-seq:(Medium) rs1299389463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99945,RMVar_hsa_circ_210419 67642 RMVar_ID_67642 Human_SNP_ID_682424576 m1A Human chr20 + 46021824 46021824 46021824 GCTGCCCCCCGCAGGGCCCGCCAGAAGCCCTGACCCAGAGTCCCGCCGGCATTCGGTCGCAGACC GCTGCCCCCCGCAGGGCCCGCCAGAAGCCCTGGCCCAGAGTCCCGCCGGCATTCGGTCGCAGACC A G SLC12A5 Ensembl:ENSG00000124140 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:46021739..46022711 26863410 MeRIP-seq:(Medium) rs569855366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2090071,Human_Splice_Rec_2090121,Human_Splice_Rec_2090123,Human_Splice_Rec_2090127,Human_Splice_Rec_2090129 67643 RMVar_ID_67643 Human_SNP_ID_682425127 m1A Human chr20 + 46023540 46023540 46023540 CTGCCTCCAGTCCTTCCCTAGCCCTCCTCCACAGAAGCCCCCCATCACTTGCAAAATAAAGGCCA CTGCCTCCAGTCCTTCCCTAGCCCTCCTCCACCGAAGCCCCCCATCACTTGCAAAATAAAGGCCA A C SLC12A5 Ensembl:ENSG00000124140 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:46023344..46023540 26863196 MeRIP-seq:(Medium) rs953833277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18951612 67644 RMVar_ID_67644 Human_SNP_ID_682437698 m1A Human chr20 - 46070390 46070390 46070390 CAGAGACATTCGAGACCCCCGAGACTTGCGGGACCACAGACATAGTAGAGATTTGCGGGATCACA CAGAGACATTCGAGACCCCCGAGACTTGCGGGTCCACAGACATAGTAGAGATTTGCGGGATCACA T A NCOA5 Ensembl:ENSG00000124160 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:46070342..46070470 26863196 MeRIP-seq:(Medium) rs1192769104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8857405,Human_RBP_ID_14120777 RMVar_hsa_circ_64004,RMVar_hsa_circ_344034,RMVar_hsa_circ_335990,RMVar_hsa_circ_297206,RMVar_hsa_circ_69527,RMVar_hsa_circ_49432,RMVar_hsa_circ_283624 67645 RMVar_ID_67645 Human_SNP_ID_682439898 m1A Human chr20 - 46079455 46079455 46079455 AGCATTGAACAGATGGGTTGATTATTCTTTTCAGATATTAATAAGGCAGCGGAAAGAAGAAATAT AGCATTGAACAGATGGGTTGATTATTCTTTTCTGATATTAATAAGGCAGCGGAAAGAAGAAATAT T A NCOA5 Ensembl:ENSG00000124160 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:46079413..46079560 26863196 MeRIP-seq:(Medium) rs778997565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2686297,Human_RBP_ID_4659881,Human_RBP_ID_22672659,Human_RBP_ID_25615101 Human_Splice_Rec_2090379 RMVar_hsa_circ_210432 67646 RMVar_ID_67646 Human_SNP_ID_682442538 m1A Human chr20 - 46089710 46089710 46089710 GACGGGGAGGCTGAGGCGGGAAGGCCCACTCGACGCGCGGCCACGGTCTCGGCTCCTCTCCGGGT GACGGGGAGGCTGAGGCGGGAAGGCCCACTCGCCGCGCGGCCACGGTCTCGGCTCCTCTCCGGGT T G NCOA5 Ensembl:ENSG00000124160 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:46089705..46089950 26863196 MeRIP-seq:(Medium) rs1417206215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244666,Human_RBP_ID_1068342,Human_RBP_ID_3655002,Human_RBP_ID_5240311,Human_RBP_ID_5385311,Human_RBP_ID_17143057,Human_RBP_ID_18495148 67647 RMVar_ID_67647 Human_SNP_ID_682508360 m1A Human chr20 - 46359107 46359107 46359107 GCTGAAAGGCGCCCAGTGGGGCCAGGTCCTGGAGAGCCTGTGGCTGAGACTGGGAAGACCAGCAG GCTGAAAGGCGCCCAGTGGGGCCAGGTCCTGGGGAGCCTGTGGCTGAGACTGGGAAGACCAGCAG T C SLC35C2 Ensembl:ENSG00000080189 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:46359102..46359320 26863196 MeRIP-seq:(Medium) rs1281993037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244144,Human_RBP_ID_5322944,Human_RBP_ID_18463411,Human_RBP_ID_22722338,Human_RBP_ID_23284443 RMVar_hsa_circ_125460,RMVar_hsa_circ_210442,RMVar_hsa_circ_76703,RMVar_hsa_circ_210441 67648 RMVar_ID_67648 Human_SNP_ID_682508374 m1A Human chr20 - 46359167 46359167 46359167 TGGGTGCAGTGTTCGTTCATTTCCTTCAGACAACGGGAAGAAAGCTGGTGTGTTTGGGGAGCTGA TGGGTGCAGTGTTCGTTCATTTCCTTCAGACAGCGGGAAGAAAGCTGGTGTGTTTGGGGAGCTGA T C SLC35C2 Ensembl:ENSG00000080189 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:46359155..46359310 26863196 MeRIP-seq:(Medium) rs1018143391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22600324 RMVar_hsa_circ_125460,RMVar_hsa_circ_210442,RMVar_hsa_circ_76703,RMVar_hsa_circ_210441 67649 RMVar_ID_67649 Human_SNP_ID_682508851 m1A Human chr20 - 46361103 46361103 46361103 GATGCCTGATATTAGATATCTAAGGGAAGAAGAGGTTAGGTAGGCATTGGATATTCTTCTGGAGT GATGCCTGATATTAGATATCTAAGGGAAGAAGGGGTTAGGTAGGCATTGGATATTCTTCTGGAGT T C SLC35C2 Ensembl:ENSG00000080189 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:46361100..46361500 26863196 MeRIP-seq:(Medium) rs1217133396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14121455 RMVar_hsa_circ_125460,RMVar_hsa_circ_210442,RMVar_hsa_circ_76703,RMVar_hsa_circ_210441 67650 RMVar_ID_67650 Human_SNP_ID_682509170 m1A Human chr20 - 46362601 46362601 46362601 TAAGGGGACCAGGAGGGGAGTAAGCCTCTACCATGAGCCAGCATTTAATGCTGTACCTGATGCCA TAAGGGGACCAGGAGGGGAGTAAGCCTCTACCGTGAGCCAGCATTTAATGCTGTACCTGATGCCA T C SLC35C2 Ensembl:ENSG00000080189 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:46362599..46362830 26863196 MeRIP-seq:(Medium) rs1010776872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9832,Human_RBP_ID_7006275 RMVar_hsa_circ_125460,RMVar_hsa_circ_210442,RMVar_hsa_circ_76703,RMVar_hsa_circ_210441 67651 RMVar_ID_67651 Human_SNP_ID_682510380 m1A Human chr20 + 46367547 46367547 46367547 TGTCCTTCCCCAGAAGGGCACTGAGGCCATCAATCCAGATGCAGTACTGTGGGGAGCAAGTTGCA TGTCCTTCCCCAGAAGGGCACTGAGGCCATCAGTCCAGATGCAGTACTGTGGGGAGCAAGTTGCA A G AL133227.1 Ensembl:ENSG00000273828 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:46367497..46368928 32194978 MeRIP-seq:(Medium) rs1233759030 Functional Loss SNV dbSNP153 33..33 33 - - - 67652 RMVar_ID_67652 Human_SNP_ID_682512117 m1A Human chr20 - 46374442 46374442 46374442 TCTCCCTAATCCTCCCTTTCTCTTCCCCCGACAGATTGTCTTGGAGAACAGTAGCCGGGAAGACA TCTCCCTAATCCTCCCTTTCTCTTCCCCCGACGGATTGTCTTGGAGAACAGTAGCCGGGAAGACA T C ELMO2 Ensembl:ENSG00000062598 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:46374396..46375337 32194978 MeRIP-seq:(Medium) rs1568753589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5385320,Human_RBP_ID_22549328,Human_RBP_ID_22670952 RMVar_hsa_circ_36647,RMVar_hsa_circ_36452,RMVar_hsa_circ_376494,RMVar_hsa_circ_210443,RMVar_hsa_circ_105379,RMVar_hsa_circ_123306,RMVar_hsa_circ_210444,RMVar_hsa_circ_25631 67653 RMVar_ID_67653 Human_SNP_ID_682512612 m1A Human chr20 - 46376545 46376545 46376545 GGAGACATAGCATGCAAGAGAAAGACAGAGACAGAACATGAGACAGGACCAGGGGACCTAAAGTG GGAGACATAGCATGCAAGAGAAAGACAGAGACCGAACATGAGACAGGACCAGGGGACCTAAAGTG T G ELMO2 Ensembl:ENSG00000062598 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:46376255..46376781 26863196 MeRIP-seq:(Medium) rs192858857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36647,RMVar_hsa_circ_376494,RMVar_hsa_circ_123306,RMVar_hsa_circ_210444,RMVar_hsa_circ_6635,RMVar_hsa_circ_25631 67654 RMVar_ID_67654 Human_SNP_ID_682514501 m1A Human chr20 - 46386187 46386187 46386187 GGCCATCCTGGAGAGCATGGTCTTGAACAGCCAGAGTCTGTACCAGAAGATAGCCGAGGAAATCA GGCCATCCTGGAGAGCATGGTCTTGAACAGCCGGAGTCTGTACCAGAAGATAGCCGAGGAAATCA T C ELMO2 Ensembl:ENSG00000062598 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:46386138..46387350 32194978 MeRIP-seq:(Medium) rs1247605228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27819851 Human_Splice_Rec_2090722,Human_Splice_Rec_2090723,Human_Splice_Rec_2090764,Human_Splice_Rec_2090765,Human_Splice_Rec_2090816,Human_Splice_Rec_2090817,Human_Splice_Rec_2090854,Human_Splice_Rec_2090855,Human_Splice_Rec_2090889,Human_Splice_Rec_2090903,Human_Splice_Rec_2090938,Human_Splice_Rec_2090939,Human_Splice_Rec_2090966,Human_Splice_Rec_2090967,Human_Splice_Rec_2090975,Human_Splice_Rec_2090992,Human_Splice_Rec_2090993,Human_Splice_Rec_2091006,Human_Splice_Rec_2091007,Human_Splice_Rec_2091022 Human_miRNA_ID_2333502,Human_miRNA_ID_2333503,Human_miRNA_ID_2966586,Human_miRNA_ID_2966587 RMVar_hsa_circ_36647,RMVar_hsa_circ_376494,RMVar_hsa_circ_123306,RMVar_hsa_circ_210444,RMVar_hsa_circ_12697,RMVar_hsa_circ_6635,RMVar_hsa_circ_360852,RMVar_hsa_circ_376147,RMVar_hsa_circ_359320,RMVar_hsa_circ_54564,RMVar_hsa_circ_210445,RMVar_hsa_circ_210446 67655 RMVar_ID_67655 Human_SNP_ID_682518941 m1A Human chr20 - 46406574 46406574 46406574 CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCAGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCGGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT T C ELMO2 Ensembl:ENSG00000062598 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs401379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659446,Human_RBP_ID_19005962 Human_Splice_Rec_2090709,Human_Splice_Rec_2090749,Human_Splice_Rec_2090803,Human_Splice_Rec_2090925,Human_Splice_Rec_2090951,Human_Splice_Rec_2090979,Human_Splice_Rec_2090995,Human_Splice_Rec_2091009 67656 RMVar_ID_67656 Human_SNP_ID_682518942 m1A Human chr20 - 46406574 46406574 46406574 CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCAGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCCGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT T G ELMO2 Ensembl:ENSG00000062598 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs401379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659446,Human_RBP_ID_19005962 Human_Splice_Rec_2090709,Human_Splice_Rec_2090749,Human_Splice_Rec_2090803,Human_Splice_Rec_2090925,Human_Splice_Rec_2090951,Human_Splice_Rec_2090979,Human_Splice_Rec_2090995,Human_Splice_Rec_2091009 67657 RMVar_ID_67657 Human_SNP_ID_682518951 m1A Human chr20 - 46406591 46406591 46406591 GGCGGGGCGGGCGGAGGCTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCAGGAGCTGGGCCTAGG GGCGGGGCGGGCGGAGGCTGGAGGAGCCGCCGCGCGGAGACCCGGGAGCAGGAGCTGGGCCTAGG T G ELMO2 Ensembl:ENSG00000062598 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:46406055..46406603 26863196 MeRIP-seq:(Medium) rs371051511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659446 Human_Splice_Rec_2090709,Human_Splice_Rec_2090749,Human_Splice_Rec_2090803,Human_Splice_Rec_2090925,Human_Splice_Rec_2090951,Human_Splice_Rec_2090979,Human_Splice_Rec_2090995,Human_Splice_Rec_2091009 67658 RMVar_ID_67658 Human_SNP_ID_682586259 m1A Human chr20 - 46689421 46689421 46689421 GAGACAGCTGATCGGTTGGAGCTGTTGCGCCGAGCAGTCATGGCGGCGGCCAGAGCTACTACGCC GAGACAGCTGATCGGTTGGAGCTGTTGCGCCGGGCAGTCATGGCGGCGGCCAGAGCTACTACGCC T C TP53RK Ensembl:ENSG00000172315 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:46689306..46689538 26863196 MeRIP-seq:(Medium) rs200458485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244602,Human_RBP_ID_779248,Human_RBP_ID_4659889,Human_RBP_ID_22081384,Human_RBP_ID_23004983 RMVar_hsa_circ_92684,RMVar_hsa_circ_210463,RMVar_hsa_circ_79740,RMVar_hsa_circ_210462 67659 RMVar_ID_67659 Human_SNP_ID_682594935 m1A Human chr20 + 46725776 46725776 46725776 GGGGCTGGTGCTCTTCCAGCAACTAACAGGGCAGCCCAACGTGCTGTGCTATGCCTCCACCATCT GGGGCTGGTGCTCTTCCAGCAACTAACAGGGCGGCCCAACGTGCTGTGCTATGCCTCCACCATCT A G SLC2A10 Ensembl:ENSG00000197496 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:46725725..46725826 32194978 MeRIP-seq:(Medium) rs1308731656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3091370 RMVar_hsa_circ_93081,RMVar_hsa_circ_210465,RMVar_hsa_circ_210464,RMVar_hsa_circ_371821 67660 RMVar_ID_67660 Human_SNP_ID_682722139 m1A Human chr20 - 47236339 47236339 47236339 TGCCTCAGCTGATGTCGCCGCTGATATTGCCAAGTACACTAGCAAAGTGAGTGGATGGGAGAGCT TGCCTCAGCTGATGTCGCCGCTGATATTGCCACGTACACTAGCAAAGTGAGTGGATGGGAGAGCT T G ZMYND8 Ensembl:ENSG00000101040 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:47236326..47236500 26863196 MeRIP-seq:(Medium) rs1381873116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8534620,Human_RBP_ID_9390867,Human_RBP_ID_26343059,Human_RBP_ID_27820359 Human_Splice_Rec_2091503,Human_Splice_Rec_2091545,Human_Splice_Rec_2091589,Human_Splice_Rec_2091631,Human_Splice_Rec_2091677,Human_Splice_Rec_2091725,Human_Splice_Rec_2091793,Human_Splice_Rec_2091835,Human_Splice_Rec_2091877,Human_Splice_Rec_2091913,Human_Splice_Rec_2091959,Human_Splice_Rec_2092003,Human_Splice_Rec_2092047,Human_Splice_Rec_2092087,Human_Splice_Rec_2092129,Human_Splice_Rec_2092173 Human_miRNA_ID_2133109 RMVar_hsa_circ_295620,RMVar_hsa_circ_73732,RMVar_hsa_circ_349408,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_210471,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_293394,RMVar_hsa_circ_27798,RMVar_hsa_circ_288021,RMVar_hsa_circ_286280,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,RMVar_hsa_circ_283612,RMVar_hsa_circ_348224,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210474,RMVar_hsa_circ_47077,RMVar_hsa_circ_210475,RMVar_hsa_circ_210473 67661 RMVar_ID_67661 Human_SNP_ID_682722911 m1A Human chr20 - 47239007 47239007 47239007 CCACAGCCACCACCAGCACGTCCTCCACGGTCACCGTCACGGCCCCGGCCCCCGCCGCCACAGGA CCACAGCCACCACCAGCACGTCCTCCACGGTCGCCGTCACGGCCCCGGCCCCCGCCGCCACAGGA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:47238957..47239084 26863196 MeRIP-seq:(Medium) rs1261419295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_27798,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,RMVar_hsa_circ_348224,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210474,RMVar_hsa_circ_47077,RMVar_hsa_circ_210473,RMVar_hsa_circ_210476,RMVar_hsa_circ_108443 67662 RMVar_ID_67662 Human_SNP_ID_682730008 m1A Human chr20 + 47266136 47266136 47266136 GCATCTCCCTGAGAAACAGGTCTCCTATGTCCACCTCCTAGTGCCACCAATCCTACCTCCCCAGT GCATCTCCCTGAGAAACAGGTCTCCTATGTCCGCCTCCTAGTGCCACCAATCCTACCTCCCCAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:47266133..47266216 26863196 MeRIP-seq:(Medium) rs1396244208 Functional Loss SNV dbSNP153 33..33 33 - - - 67663 RMVar_ID_67663 Human_SNP_ID_682733854 m1A Human chr20 - 47280768 47280768 47280768 GAGGGGTAGGCAGGAGTTTGTTTTTTATTTGAAGAGCAGGAGGAATTGGTGACAGGCTGTACATC GAGGGGTAGGCAGGAGTTTGTTTTTTATTTGAGGAGCAGGAGGAATTGGTGACAGGCTGTACATC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:47280756..47280936 26863196 MeRIP-seq:(Medium) rs1244236635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_363044,RMVar_hsa_circ_55827,RMVar_hsa_circ_22019,RMVar_hsa_circ_124292,RMVar_hsa_circ_45071,RMVar_hsa_circ_278493,RMVar_hsa_circ_291951,RMVar_hsa_circ_333651,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_12782,RMVar_hsa_circ_210483,RMVar_hsa_circ_297931,RMVar_hsa_circ_344781,RMVar_hsa_circ_371021,RMVar_hsa_circ_210481,RMVar_hsa_circ_345800,RMVar_hsa_circ_317169,RMVar_hsa_circ_302234,RMVar_hsa_circ_279468,RMVar_hsa_circ_294255,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_27851,RMVar_hsa_circ_285218,RMVar_hsa_circ_309820,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487,RMVar_hsa_circ_319203,RMVar_hsa_circ_324384,RMVar_hsa_circ_307901,RMVar_hsa_circ_309071,RMVar_hsa_circ_279185,RMVar_hsa_circ_283317,RMVar_hsa_circ_60377,RMVar_hsa_circ_210497,RMVar_hsa_circ_210499,RMVar_hsa_circ_210498,RMVar_hsa_circ_210501 67664 RMVar_ID_67664 Human_SNP_ID_682753465 m1A Human chr20 - 47356612 47356612 47356612 TTTTAACCATCTTTTTTCCCCCTCCCTCTGAGACATCCGAATTGTGGGCGAGCAGTGTGATTTCT TTTTAACCATCTTTTTTCCCCCTCCCTCTGAGCCATCCGAATTGTGGGCGAGCAGTGTGATTTCT T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:47356596..47356667;chr20:47356603..47356676 26863196 MeRIP-seq:(Medium) rs760962423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19106710,Human_RBP_ID_22361682,Human_RBP_ID_23907901,Human_RBP_ID_24491958,Human_RBP_ID_25616095 RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_12782,RMVar_hsa_circ_27851,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294 67665 RMVar_ID_67665 Human_SNP_ID_682791509 m1A Human chr20 + 47501968 47501948 47501969 AGTCGGTGGCGGCCGGCGGCGGCTGCGGGCTGAGCGGCGAGTTTCCGATTTAAAGCTGAGCTGCG AGTCGGTGGCGGC_____________________CGGCGAGTTTCCGATTTAAAGCTGAGCTGCG CCGGCGGCGGCTGCGGGCTGAG C NCOA3 Ensembl:ENSG00000124151 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:47501923..47502217 26863196 MeRIP-seq:(Medium) rs1049187849 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_831685,Human_RBP_ID_4659449,Human_RBP_ID_5423790,Human_RBP_ID_8857524,Human_RBP_ID_9331555,Human_RBP_ID_23115469,Human_RBP_ID_23133771,Human_RBP_ID_23907913 Human_Splice_Rec_2092243,Human_Splice_Rec_2092285,Human_Splice_Rec_2092327 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 67666 RMVar_ID_67666 Human_SNP_ID_682830048 m1A Human chr20 + 47651121 47651101 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAG_____________________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAGCAGCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs747048800 Functional Loss DEL dbSNP153 14..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67667 RMVar_ID_67667 Human_SNP_ID_682830053 m1A Human chr20 + 47651121 47651104 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAG__________________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAGCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs776768853 Functional Loss DEL dbSNP153 17..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67668 RMVar_ID_67668 Human_SNP_ID_682830057 m1A Human chr20 + 47651121 47651107 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAG_______________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs762770921 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67669 RMVar_ID_67669 Human_SNP_ID_682830067 m1A Human chr20 + 47651121 47651110 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAG____________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs761853828 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67670 RMVar_ID_67670 Human_SNP_ID_682830070 m1A Human chr20 + 47651121 47651113 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAGCAG_________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs749960421 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67671 RMVar_ID_67671 Human_SNP_ID_682830080 m1A Human chr20 + 47651121 47651119 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAGCAGCAGCAG___CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112826888 Functional Loss DEL dbSNP153,HGVD 32..34 33 - - - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 67672 RMVar_ID_67672 Human_SNP_ID_682837401 m1A Human chr20 - 47676469 47676469 47676469 TGGGACAGGTAAGAAGGCTCCCTTCCCTCCCAACGGCTCCCCCTCCTGACTGCAGCCGGCCCTGA TGGGACAGGTAAGAAGGCTCCCTTCCCTCCCAGCGGCTCCCCCTCCTGACTGCAGCCGGCCCTGA T C SULF2 Ensembl:ENSG00000196562 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:47676464..47676566 26863196 MeRIP-seq:(Medium) rs779712340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12994,RMVar_hsa_circ_103752,RMVar_hsa_circ_111250,RMVar_hsa_circ_210543,RMVar_hsa_circ_210545,RMVar_hsa_circ_86367,RMVar_hsa_circ_210547 67673 RMVar_ID_67673 Human_SNP_ID_683089953 m1A Human chr20 - 48642264 48642264 48642264 ACGGGGCCCAAACCAACCCCAGGCTTCTTGCCACCCAGGTGGACTCCATCAATGCTCTCCTCAAG ACGGGGCCCAAACCAACCCCAGGCTTCTTGCCCCCCAGGTGGACTCCATCAATGCTCTCCTCAAG T G PREX1 Ensembl:ENSG00000124126 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:48642258..48642395 32194978 MeRIP-seq:(Medium) rs764392160 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_2092705,Human_Splice_Rec_2092781 RMVar_hsa_circ_15002,RMVar_hsa_circ_121864,RMVar_hsa_circ_85593,RMVar_hsa_circ_210552,RMVar_hsa_circ_210553,RMVar_hsa_circ_70266,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_293892,RMVar_hsa_circ_353578,RMVar_hsa_circ_269799,RMVar_hsa_circ_210555 67674 RMVar_ID_67674 Human_SNP_ID_683102450 m1A Human chr20 - 48688790 48688790 48688790 GACCGTGCCCCTGTGTAGGCCTGAAGCTGGGCATGGAGCGTGATGCCTACGTCATGATTGCGGAG GACCGTGCCCCTGTGTAGGCCTGAAGCTGGGCGTGGAGCGTGATGCCTACGTCATGATTGCGGAG T C PREX1 Ensembl:ENSG00000124126 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:48688740..48688830 26863196 MeRIP-seq:(Medium) rs1171926006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2092742 Human_miRNA_ID_2897330 RMVar_hsa_circ_85593,RMVar_hsa_circ_210553,RMVar_hsa_circ_18858,RMVar_hsa_circ_105009,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_107290,RMVar_hsa_circ_95883,RMVar_hsa_circ_210556,RMVar_hsa_circ_210557,RMVar_hsa_circ_267852,RMVar_hsa_circ_210558,RMVar_hsa_circ_111033,RMVar_hsa_circ_210560,RMVar_hsa_circ_330802,RMVar_hsa_circ_116400,RMVar_hsa_circ_56426,RMVar_hsa_circ_210561,RMVar_hsa_circ_49220,RMVar_hsa_circ_70706,RMVar_hsa_circ_34101,RMVar_hsa_circ_5369,RMVar_hsa_circ_38008,RMVar_hsa_circ_22281,RMVar_hsa_circ_349405,RMVar_hsa_circ_353134,RMVar_hsa_circ_348050,RMVar_hsa_circ_319027,RMVar_hsa_circ_210562,RMVar_hsa_circ_265786,RMVar_hsa_circ_39245,RMVar_hsa_circ_369719,RMVar_hsa_circ_210564,RMVar_hsa_circ_210565,RMVar_hsa_circ_376338,RMVar_hsa_circ_306862,RMVar_hsa_circ_326550,RMVar_hsa_circ_61455,RMVar_hsa_circ_210566,RMVar_hsa_circ_210567 67675 RMVar_ID_67675 Human_SNP_ID_683105241 m1A Human chr20 - 48699937 48699937 48699937 GAGGCAGGGAGGGAAGGAAGGAATGTGGACGGATGTTGGAATTGACGTGTGTGTGAGTGAATGAG GAGGCAGGGAGGGAAGGAAGGAATGTGGACGGCTGTTGGAATTGACGTGTGTGTGAGTGAATGAG T G PREX1 Ensembl:ENSG00000124126 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:48699914..48700052 26863196 MeRIP-seq:(Medium) rs1323619111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18858,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_49220,RMVar_hsa_circ_34101,RMVar_hsa_circ_49296,RMVar_hsa_circ_5369,RMVar_hsa_circ_38008,RMVar_hsa_circ_349405,RMVar_hsa_circ_353134,RMVar_hsa_circ_369719,RMVar_hsa_circ_61455,RMVar_hsa_circ_210567,RMVar_hsa_circ_210569,RMVar_hsa_circ_126834 67676 RMVar_ID_67676 Human_SNP_ID_683159735 m1A Human chr20 - 48921298 48921298 48921298 GAGTAGGAAAGAAAAGAGGTGAGGGAGCGAGGACTGGAAGCTGGTGAATGAATGAGAAGTGATCG GAGTAGGAAAGAAAAGAGGTGAGGGAGCGAGGCCTGGAAGCTGGTGAATGAATGAGAAGTGATCG T G lnc-PREX1-10,lnc-PREX1-10:2 RNACentral:URS0000D5BF89,RNACentral:URS0000D593F2 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:48921248..48921583 26863196 MeRIP-seq:(Medium) rs1316588301 Functional Loss SNV dbSNP153 33..33 33 - - - 67677 RMVar_ID_67677 Human_SNP_ID_683162421 m1A Human chr20 + 48931878 48931878 48931878 ATTTTACGCGGAGTGGGATGGAAAGCTACTGGAGCATTTTGAGCAAAGGAGTGTTGTGATCTGAG ATTTTACGCGGAGTGGGATGGAAAGCTACTGGGGCATTTTGAGCAAAGGAGTGTTGTGATCTGAG A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:48931498..48932396 26863196 MeRIP-seq:(Medium) rs1246809229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14125249 RMVar_hsa_circ_210575 67678 RMVar_ID_67678 Human_SNP_ID_683168210 m1A Human chr20 - 48953699 48953699 48953699 GAATCACTCCTGGCATGTTCACCGTTGGTTAAATCTGTTTTTTCGGGAGTTGTTGGTTTGCTTTG GAATCACTCCTGGCATGTTCACCGTTGGTTAAGTCTGTTTTTTCGGGAGTTGTTGGTTTGCTTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:48953649..48953739 26863196 MeRIP-seq:(Medium) rs1272004895 Functional Loss SNV dbSNP153 33..33 33 - - - 67679 RMVar_ID_67679 Human_SNP_ID_683191155 m1A Human chr20 - 49046376 49046376 49046376 AAACGGAGGAGGGAACCCCAGCCGCGGACCGTAGCTGGCACTACCCGCTCCTGCCGCCGCTCCGC AAACGGAGGAGGGAACCCCAGCCGCGGACCGTGGCTGGCACTACCCGCTCCTGCCGCCGCTCCGC T C CSE1L-AS1,CSE1L-AS1:2 RNACentral:URS0000D5B049,RNACentral:URS0000D5B116 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49046326..49046508 26863196 MeRIP-seq:(Medium) rs1202761694 Functional Loss SNV dbSNP153 33..33 33 - - - 67680 RMVar_ID_67680 Human_SNP_ID_683191156 m1A Human chr20 + 49046377 49046377 49046377 CGGAGCGGCGGCAGGAGCGGGTAGTGCCAGCTACGGTCCGCGGCTGGGGTTCCCTCCTCCGTTTC CGGAGCGGCGGCAGGAGCGGGTAGTGCCAGCTGCGGTCCGCGGCTGGGGTTCCCTCCTCCGTTTC A G CSE1L Ensembl:ENSG00000124207 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:49046326..49046508;chr20:49046326..49046484;chr20:49046326..49046505;chr20:49046326..49046466 26863196 MeRIP-seq:(Medium) rs1442107579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565696,Human_RBP_ID_4659893,Human_RBP_ID_5322946,Human_RBP_ID_8534907,Human_RBP_ID_9331556,Human_RBP_ID_18422916,Human_RBP_ID_18774588,Human_RBP_ID_22080702,Human_RBP_ID_27022175,Human_RBP_ID_27297963 Human_Splice_Rec_2092897,Human_Splice_Rec_2092943 RMVar_hsa_circ_108495,RMVar_hsa_circ_210655 67681 RMVar_ID_67681 Human_SNP_ID_683194602 m1A Human chr20 + 49058469 49058469 49058469 TTATTTTATATTTTAGATCCTATAGCAATGGAACTCAGCGATGCAAATCTGCAAACACTAACAGA TTATTTTATATTTTAGATCCTATAGCAATGGACCTCAGCGATGCAAATCTGCAAACACTAACAGA A C CSE1L Ensembl:ENSG00000124207 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:49058451..49058475 26863196 MeRIP-seq:(Medium) rs752585427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62663,Human_RBP_ID_1598355,Human_RBP_ID_1930863,Human_RBP_ID_4659895,Human_RBP_ID_9331903,Human_RBP_ID_9390918,Human_RBP_ID_14126863,Human_RBP_ID_18774596,Human_RBP_ID_26494130 Human_Splice_Rec_2092898,Human_Splice_Rec_2092899,Human_Splice_Rec_2092944,Human_Splice_Rec_2092945 RMVar_hsa_circ_44091,RMVar_hsa_circ_63246,RMVar_hsa_circ_108495,RMVar_hsa_circ_315832,RMVar_hsa_circ_368110,RMVar_hsa_circ_210655,RMVar_hsa_circ_329602,RMVar_hsa_circ_300449,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_210657,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210658,RMVar_hsa_circ_210656 67682 RMVar_ID_67682 Human_SNP_ID_683194611 m1A Human chr20 + 49058501 49058501 49058501 ACTCAGCGATGCAAATCTGCAAACACTAACAGAATATTTAAAGAAAACACTTGATCCTGATCCTG ACTCAGCGATGCAAATCTGCAAACACTAACAGTATATTTAAAGAAAACACTTGATCCTGATCCTG A T CSE1L Ensembl:ENSG00000124207 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:49058451..49058500 26863196 MeRIP-seq:(Medium) rs1400028356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1135845,Human_RBP_ID_1930864,Human_RBP_ID_3650437,Human_RBP_ID_4659895,Human_RBP_ID_18323058 Human_Splice_Rec_2092898,Human_Splice_Rec_2092899,Human_Splice_Rec_2092944,Human_Splice_Rec_2092945 RMVar_hsa_circ_44091,RMVar_hsa_circ_63246,RMVar_hsa_circ_108495,RMVar_hsa_circ_315832,RMVar_hsa_circ_368110,RMVar_hsa_circ_210655,RMVar_hsa_circ_329602,RMVar_hsa_circ_300449,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_210657,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210658,RMVar_hsa_circ_210656 67683 RMVar_ID_67683 Human_SNP_ID_683205182 m1A Human chr20 + 49096669 49096669 49096669 CTTCTAGTTTGCAACTTCAAGGGACAAGTATTAATAGTTCAGTGTATGGCGTTGGTTTGTGTTGA CTTCTAGTTTGCAACTTCAAGGGACAAGTATTGATAGTTCAGTGTATGGCGTTGGTTTGTGTTGA A G CSE1L Ensembl:ENSG00000124207 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49096618..49096740 26863196 MeRIP-seq:(Medium) rs1568792035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1026458,Human_RBP_ID_1198656,Human_RBP_ID_1598472,Human_RBP_ID_1930980,Human_RBP_ID_2687140,Human_RBP_ID_3650522,Human_RBP_ID_14128264,Human_RBP_ID_17512046,Human_RBP_ID_17700662,Human_RBP_ID_17973243,Human_RBP_ID_18774709,Human_RBP_ID_23212470,Human_RBP_ID_23908639,Human_RBP_ID_27702604 RMVar_hsa_circ_96527,RMVar_hsa_circ_210709 67684 RMVar_ID_67684 Human_SNP_ID_683210470 m1A Human chr20 - 49114621 49114621 49114621 CCCTACGCAATAGCAGCTGCCTGTGGGGAAGAAGGGCTGCCCAGCCAGCTGGTTCTCCCGGGACA CCCTACGCAATAGCAGCTGCCTGTGGGGAAGAGGGGCTGCCCAGCCAGCTGGTTCTCCCGGGACA T C STAU1 Ensembl:ENSG00000124214 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1043361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529165,Human_RBP_ID_7008734,Human_RBP_ID_22081395,Human_RBP_ID_22395553 Human_miRNA_ID_175661,Human_miRNA_ID_178130 GWAS_ID_8096,GWAS_ID_8097,GWAS_ID_8098,GWAS_ID_8099 67685 RMVar_ID_67685 Human_SNP_ID_683210471 m1A Human chr20 - 49114621 49114621 49114621 CCCTACGCAATAGCAGCTGCCTGTGGGGAAGAAGGGCTGCCCAGCCAGCTGGTTCTCCCGGGACA CCCTACGCAATAGCAGCTGCCTGTGGGGAAGACGGGCTGCCCAGCCAGCTGGTTCTCCCGGGACA T G STAU1 Ensembl:ENSG00000124214 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1043361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529165,Human_RBP_ID_7008734,Human_RBP_ID_22081395,Human_RBP_ID_22395553 Human_miRNA_ID_175661,Human_miRNA_ID_178130 GWAS_ID_8096,GWAS_ID_8097,GWAS_ID_8098,GWAS_ID_8099 67686 RMVar_ID_67686 Human_SNP_ID_683210506 m1A Human chr20 - 49114723 49114723 49114723 GTGGGCAGCAGCAGGGAAGACAACAGAAACACAAGGAGGCGGCTGTGGCCGGGCTGGACTGTGCT GTGGGCAGCAGCAGGGAAGACAACAGAAACACGAGGAGGCGGCTGTGGCCGGGCTGGACTGTGCT T C STAU1 Ensembl:ENSG00000124214 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49114629..49114824 26863196 MeRIP-seq:(Medium) rs1263441032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4664489,Human_RBP_ID_7008739,Human_RBP_ID_8535055,Human_RBP_ID_14128716,Human_RBP_ID_17973264,Human_RBP_ID_22395304,Human_RBP_ID_26491307,Human_RBP_ID_27298041,Human_RBP_ID_27486704 67687 RMVar_ID_67687 Human_SNP_ID_683210822 m1A Human chr20 - 49115826 49115826 49115826 AACATCTTAAAGTTGCTGTCTGAGTTGGACCAACAAAGTACAGAGATGCCAAGAACAGGAAACGG AACATCTTAAAGTTGCTGTCTGAGTTGGACCAGCAAAGTACAGAGATGCCAAGAACAGGAAACGG T C STAU1 Ensembl:ENSG00000124214 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:49115823..49117232 32194978 MeRIP-seq:(Medium) rs755888494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9117841,Human_RBP_ID_26821465 Human_Splice_Rec_2093024,Human_Splice_Rec_2093025,Human_Splice_Rec_2093044,Human_Splice_Rec_2093045,Human_Splice_Rec_2093068,Human_Splice_Rec_2093069,Human_Splice_Rec_2093092,Human_Splice_Rec_2093093,Human_Splice_Rec_2093114,Human_Splice_Rec_2093115,Human_Splice_Rec_2093140,Human_Splice_Rec_2093141,Human_Splice_Rec_2093162,Human_Splice_Rec_2093163,Human_Splice_Rec_2093184,Human_Splice_Rec_2093185 RMVar_hsa_circ_41102,RMVar_hsa_circ_110815,RMVar_hsa_circ_340131,RMVar_hsa_circ_346187,RMVar_hsa_circ_314425,RMVar_hsa_circ_85844,RMVar_hsa_circ_210723,RMVar_hsa_circ_210724,RMVar_hsa_circ_210725 67688 RMVar_ID_67688 Human_SNP_ID_683211330 m1A Human chr20 + 49117829 49117829 49117829 AAAGATAGTCCAGTTGCTCAGAGGGTCTCGTGAGAGGTCCATGGGGTACGTGGCCTGAAGAGATG AAAGATAGTCCAGTTGCTCAGAGGGTCTCGTGGGAGGTCCATGGGGTACGTGGCCTGAAGAGATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49117778..49117945 26863196 MeRIP-seq:(Medium) rs1568814635 Functional Loss SNV dbSNP153 33..33 33 - - - 67689 RMVar_ID_67689 Human_SNP_ID_683213035 m1A Human chr20 - 49124426 49124426 49124426 GAGGAGCTGAAGAAGTTACCGCCCCTGCCTGCAGTTGAACGAGTAAAGCCTAGAATCAAAAAGAA GAGGAGCTGAAGAAGTTACCGCCCCTGCCTGCCGTTGAACGAGTAAAGCCTAGAATCAAAAAGAA T G STAU1 Ensembl:ENSG00000124214 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49124325..49124531 26863196 MeRIP-seq:(Medium) rs898561394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565792,Human_RBP_ID_926628,Human_RBP_ID_1380457,Human_RBP_ID_7008782,Human_RBP_ID_9389478,Human_RBP_ID_14128795,Human_RBP_ID_17512884,Human_RBP_ID_23908712,Human_RBP_ID_26343080 Human_Splice_Rec_2093013,Human_Splice_Rec_2093033,Human_Splice_Rec_2093057,Human_Splice_Rec_2093081,Human_Splice_Rec_2093103,Human_Splice_Rec_2093129,Human_Splice_Rec_2093151,Human_Splice_Rec_2093173 RMVar_hsa_circ_41102,RMVar_hsa_circ_110815,RMVar_hsa_circ_340131,RMVar_hsa_circ_346187,RMVar_hsa_circ_314425,RMVar_hsa_circ_85844,RMVar_hsa_circ_210723,RMVar_hsa_circ_210724,RMVar_hsa_circ_210725,RMVar_hsa_circ_303409,RMVar_hsa_circ_347298,RMVar_hsa_circ_321909,RMVar_hsa_circ_123744,RMVar_hsa_circ_56047,RMVar_hsa_circ_61873,RMVar_hsa_circ_210728,RMVar_hsa_circ_210729,RMVar_hsa_circ_210727,RMVar_hsa_circ_210732,RMVar_hsa_circ_74881,RMVar_hsa_circ_301408,RMVar_hsa_circ_360123,RMVar_hsa_circ_311217,RMVar_hsa_circ_81836,RMVar_hsa_circ_44081,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_21386,RMVar_hsa_circ_365227,RMVar_hsa_circ_210734 67690 RMVar_ID_67690 Human_SNP_ID_683221431 m1A Human chr20 - 49154022 49154022 49154022 GTAGAACTAAATGCACTGTGCATGAAACTTGGAAAAAAACCAATGTATAAGCCTGTTGACCCTTA GTAGAACTAAATGCACTGTGCATGAAACTTGGGAAAAAACCAATGTATAAGCCTGTTGACCCTTA T C STAU1 Ensembl:ENSG00000124214 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:49151695..49158446 32194978 MeRIP-seq:(Medium) rs1231158367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565804,Human_RBP_ID_1598546,Human_RBP_ID_1931044,Human_RBP_ID_4651240,Human_RBP_ID_17282827,Human_RBP_ID_18774773,Human_RBP_ID_23908774 Human_Splice_Rec_2093006,Human_Splice_Rec_2093007,Human_Splice_Rec_2093027,Human_Splice_Rec_2093050,Human_Splice_Rec_2093051,Human_Splice_Rec_2093074,Human_Splice_Rec_2093075,Human_Splice_Rec_2093096,Human_Splice_Rec_2093097,Human_Splice_Rec_2093122,Human_Splice_Rec_2093123,Human_Splice_Rec_2093144,Human_Splice_Rec_2093145,Human_Splice_Rec_2093166,Human_Splice_Rec_2093167,Human_Splice_Rec_2093192,Human_Splice_Rec_2093193,Human_Splice_Rec_2093203 RMVar_hsa_circ_346187,RMVar_hsa_circ_314425,RMVar_hsa_circ_210723,RMVar_hsa_circ_303409,RMVar_hsa_circ_123744,RMVar_hsa_circ_61873,RMVar_hsa_circ_210728,RMVar_hsa_circ_210729,RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_360123,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_365227,RMVar_hsa_circ_210734,RMVar_hsa_circ_288382,RMVar_hsa_circ_288841,RMVar_hsa_circ_303101,RMVar_hsa_circ_283261,RMVar_hsa_circ_210737,RMVar_hsa_circ_210738,RMVar_hsa_circ_210736,RMVar_hsa_circ_210742,RMVar_hsa_circ_210744,RMVar_hsa_circ_280211,RMVar_hsa_circ_351587,RMVar_hsa_circ_353726,RMVar_hsa_circ_319081,RMVar_hsa_circ_111014,RMVar_hsa_circ_210743,RMVar_hsa_circ_271020,RMVar_hsa_circ_364738,RMVar_hsa_circ_210741,RMVar_hsa_circ_359176 67691 RMVar_ID_67691 Human_SNP_ID_683230941 m1A Human chr20 + 49188185 49188185 49188185 CCTGGGCGGTGGCGGCGAGGAGGGGAAGGAAGAAGGAAAAAAGGGAGAGGAAGAAGGGACGAAGG CCTGGGCGGTGGCGGCGAGGAGGGGAAGGAAGTAGGAAAAAAGGGAGAGGAAGAAGGGACGAAGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:49188010..49188334 26863196 MeRIP-seq:(Medium) rs1467938072 Functional Loss SNV dbSNP153 33..33 33 - - - 67692 RMVar_ID_67692 Human_SNP_ID_683230993 m1A Human chr20 + 49188274 49188273 49188274 GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGAGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGG_GGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC GA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:49188176..49188350;chr20:49188126..49188375;chr20:49188213..49188317 26863410 MeRIP-seq:(Medium) rs1184232420 Functional Loss DEL dbSNP153 33..33 33 - - - 67693 RMVar_ID_67693 Human_SNP_ID_683230997 m1A Human chr20 + 49188274 49188274 49188274 GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGAGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGCGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:49188176..49188350;chr20:49188126..49188375;chr20:49188213..49188317 26863410 MeRIP-seq:(Medium) rs899220296 Functional Loss SNV dbSNP153 33..33 33 - - - 67694 RMVar_ID_67694 Human_SNP_ID_683230998 m1A Human chr20 + 49188274 49188274 49188274 GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGAGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGGGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:49188176..49188350;chr20:49188126..49188375;chr20:49188213..49188317 26863410 MeRIP-seq:(Medium) rs899220296 Functional Loss SNV dbSNP153 33..33 33 - - - 67695 RMVar_ID_67695 Human_SNP_ID_683231003 m1A Human chr20 - 49188280 49188280 49188280 TGCCGCGTCTCTCTCGGCTCCCGCTTCCTTTGACCGCCTCCCCCCCCCGGCCCGGCGGCGCCCGC TGCCGCGTCTCTCTCGGCTCCCGCTTCCTTTGGCCGCCTCCCCCCCCCGGCCCGGCGGCGCCCGC T C STAU1 Ensembl:ENSG00000124214 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:49188216..49188324 26863410 MeRIP-seq:(Medium) rs1206419586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659896,Human_RBP_ID_5275822,Human_RBP_ID_5445703,Human_RBP_ID_5471976,Human_RBP_ID_18951698 67696 RMVar_ID_67696 Human_SNP_ID_683240108 m1A Human chr20 + 49219476 49219476 49219476 ACAACATGCTTGCGGACCTCGGCTTAATCGGAACCATAGGCGAGGATGACGAGGTGCCGGTGGAG ACAACATGCTTGCGGACCTCGGCTTAATCGGAGCCATAGGCGAGGATGACGAGGTGCCGGTGGAG A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:49219426..49221453 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9389481,Human_RBP_ID_14129734,Human_RBP_ID_24546684,Human_RBP_ID_26343735 Human_Splice_Rec_2093205,Human_Splice_Rec_2093245,Human_Splice_Rec_2093285,Human_Splice_Rec_2093321,Human_Splice_Rec_2093361 RMVar_hsa_circ_113929,RMVar_hsa_circ_210750 67697 RMVar_ID_67697 Human_SNP_ID_683240135 m1A Human chr20 + 49219535 49219535 49219535 GTGGAGCCCGAGTCTGACTCCGGGGACGAGGAAGAGGAGGTATGAGCACGGTTCTGGTCTTTGGG GTGGAGCCCGAGTCTGACTCCGGGGACGAGGAGGAGGAGGTATGAGCACGGTTCTGGTCTTTGGG A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49219376..49221650 26863196 MeRIP-seq:(Medium) rs746432078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244398,Human_RBP_ID_831879,Human_RBP_ID_9389481,Human_RBP_ID_19004416,Human_RBP_ID_24546684,Human_RBP_ID_26343083,Human_RBP_ID_27820389 Human_Splice_Rec_2093205,Human_Splice_Rec_2093245,Human_Splice_Rec_2093285,Human_Splice_Rec_2093321,Human_Splice_Rec_2093361 RMVar_hsa_circ_113929,RMVar_hsa_circ_210750 67698 RMVar_ID_67698 Human_SNP_ID_683240717 m1A Human chr20 - 49221517 49221517 49221517 TACGTCCCCTCCTTCTCAGTGAAAACGAAATCAGGGTTGAAATCAGCACTGCGGTTCTTCCCCAA TACGTCCCCTCCTTCTCAGTGAAAACGAAATCGGGGTTGAAATCAGCACTGCGGTTCTTCCCCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:49219443..49223409 32194978 MeRIP-seq:(Medium) rs1453637369 Functional Loss SNV dbSNP153 33..33 33 - - - 67699 RMVar_ID_67699 Human_SNP_ID_683241193 m1A Human chr20 + 49223289 49223289 49223289 TTTTTTCCCAGGATAAAGAAGCCAAGTCTGGGAAGTTGGAAAAGGAGAAAGAAGCAAAGGAAGGC TTTTTTCCCAGGATAAAGAAGCCAAGTCTGGGGAGTTGGAAAAGGAGAAAGAAGCAAAGGAAGGC A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:49219384..49223393 26863196 MeRIP-seq:(Medium) rs1393893589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62739,Human_RBP_ID_244400,Human_RBP_ID_264708,Human_RBP_ID_831881,Human_RBP_ID_924064,Human_RBP_ID_1026475,Human_RBP_ID_1601131,Human_RBP_ID_9348057,Human_RBP_ID_23908819,Human_RBP_ID_24546687,Human_RBP_ID_26343086,Human_RBP_ID_27819890 Human_Splice_Rec_2093210,Human_Splice_Rec_2093250,Human_Splice_Rec_2093290,Human_Splice_Rec_2093326,Human_Splice_Rec_2093366 RMVar_hsa_circ_2146,RMVar_hsa_circ_116728,RMVar_hsa_circ_113929,RMVar_hsa_circ_210750,RMVar_hsa_circ_64034,RMVar_hsa_circ_210751 67700 RMVar_ID_67700 Human_SNP_ID_683241198 m1A Human chr20 + 49223302 49223302 49223302 TAAAGAAGCCAAGTCTGGGAAGTTGGAAAAGGAGAAAGAAGCAAAGGAAGGCTCTGAACCAAAGG TAAAGAAGCCAAGTCTGGGAAGTTGGAAAAGGCGAAAGAAGCAAAGGAAGGCTCTGAACCAAAGG A C DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:49219426..49223366 26863196 MeRIP-seq:(Medium) rs375052965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62739,Human_RBP_ID_244400,Human_RBP_ID_264708,Human_RBP_ID_831881,Human_RBP_ID_924064,Human_RBP_ID_1601131,Human_RBP_ID_9348057,Human_RBP_ID_9389483,Human_RBP_ID_23908819,Human_RBP_ID_24546687,Human_RBP_ID_26343086,Human_RBP_ID_27819890 Human_Splice_Rec_2093210,Human_Splice_Rec_2093250,Human_Splice_Rec_2093290,Human_Splice_Rec_2093326,Human_Splice_Rec_2093366 RMVar_hsa_circ_2146,RMVar_hsa_circ_116728,RMVar_hsa_circ_113929,RMVar_hsa_circ_210750,RMVar_hsa_circ_64034,RMVar_hsa_circ_210751 67701 RMVar_ID_67701 Human_SNP_ID_683241672 m1A Human chr20 + 49225020 49225020 49225020 ACAGGTGAGCTTGGGGCTGCAAGACAGTATGCAGCTTGTTGGCAAACCGAAAGGAGTTTAAGGTC ACAGGTGAGCTTGGGGCTGCAAGACAGTATGCGGCTTGTTGGCAAACCGAAAGGAGTTTAAGGTC A G DDX27 Ensembl:ENSG00000124228 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:49225016..49225089 26863196 MeRIP-seq:(Medium) rs753509476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19108787 Human_Splice_Rec_2093212,Human_Splice_Rec_2093252,Human_Splice_Rec_2093292,Human_Splice_Rec_2093328 RMVar_hsa_circ_116728,RMVar_hsa_circ_113929,RMVar_hsa_circ_210750,RMVar_hsa_circ_64034,RMVar_hsa_circ_554,RMVar_hsa_circ_210751 67702 RMVar_ID_67702 Human_SNP_ID_683244245 m1A Human chr20 + 49233656 49233656 49233656 CAACACAGATGTGGCTCCCTTCCTGCGGCAGGAGTTCATCCGGATCCGGCCTAATCGTGAAGGAG CAACACAGATGTGGCTCCCTTCCTGCGGCAGGGGTTCATCCGGATCCGGCCTAATCGTGAAGGAG A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:49233606..49233855 32194978 MeRIP-seq:(Medium) rs770451194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62747,Human_RBP_ID_832112,Human_RBP_ID_924941,Human_RBP_ID_9389492,Human_RBP_ID_19004419,Human_RBP_ID_23004988 Human_Splice_Rec_2093224,Human_Splice_Rec_2093225,Human_Splice_Rec_2093264,Human_Splice_Rec_2093265,Human_Splice_Rec_2093304,Human_Splice_Rec_2093340,Human_Splice_Rec_2093341,Human_Splice_Rec_2093386 Human_miRNA_ID_1983568 RMVar_hsa_circ_14699,RMVar_hsa_circ_116728,RMVar_hsa_circ_16260,RMVar_hsa_circ_118694,RMVar_hsa_circ_210751,RMVar_hsa_circ_210752,RMVar_hsa_circ_311697,RMVar_hsa_circ_19186,RMVar_hsa_circ_338735,RMVar_hsa_circ_324206,RMVar_hsa_circ_114490,RMVar_hsa_circ_277574,RMVar_hsa_circ_78624,RMVar_hsa_circ_28237,RMVar_hsa_circ_210755,RMVar_hsa_circ_210757,RMVar_hsa_circ_210758,RMVar_hsa_circ_210756,RMVar_hsa_circ_52642 67703 RMVar_ID_67703 Human_SNP_ID_683245596 m1A Human chr20 + 49239049 49239049 49239049 GAGGCGGAGGAAAAAGAGATGCAGCAGTCAGAAGCCCAGGTGAGGCTGCGAGGCGGGATCTTGTT GAGGCGGAGGAAAAAGAGATGCAGCAGTCAGAGGCCCAGGTGAGGCTGCGAGGCGGGATCTTGTT A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49239002..49239100 26863196 MeRIP-seq:(Medium) rs759450318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9389496,Human_RBP_ID_18193783,Human_RBP_ID_19006008,Human_RBP_ID_19106763,Human_RBP_ID_22081080,Human_RBP_ID_24546691,Human_RBP_ID_26343096 Human_Splice_Rec_2093233,Human_Splice_Rec_2093273,Human_Splice_Rec_2093309,Human_Splice_Rec_2093349,Human_Splice_Rec_2093389 RMVar_hsa_circ_14699,RMVar_hsa_circ_324206,RMVar_hsa_circ_114490,RMVar_hsa_circ_78624,RMVar_hsa_circ_210757,RMVar_hsa_circ_210758,RMVar_hsa_circ_5898 67704 RMVar_ID_67704 Human_SNP_ID_683246324 m1A Human chr20 + 49241950 49241950 49241950 CTTGGCCTTAAGAGGAAAGAAGAAAAGGAAGAAGTTTATGAAGGATGCCAAAAAAAAGGGGGAGA CTTGGCCTTAAGAGGAAAGAAGAAAAGGAAGAGGTTTATGAAGGATGCCAAAAAAAAGGGGGAGA A G DDX27 Ensembl:ENSG00000124228 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:49238951..49244614 26863196 MeRIP-seq:(Medium) rs773946882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1601132,Human_RBP_ID_1931075,Human_RBP_ID_3650637,Human_RBP_ID_3960911,Human_RBP_ID_7009073,Human_RBP_ID_8234883,Human_RBP_ID_9347923,Human_RBP_ID_24546777,Human_RBP_ID_26343745 Human_Splice_Rec_2093236,Human_Splice_Rec_2093237,Human_Splice_Rec_2093276,Human_Splice_Rec_2093277,Human_Splice_Rec_2093312,Human_Splice_Rec_2093313,Human_Splice_Rec_2093352,Human_Splice_Rec_2093353,Human_Splice_Rec_2093392,Human_Splice_Rec_2093393 Human_miRNA_ID_2196286 RMVar_hsa_circ_14699,RMVar_hsa_circ_114490,RMVar_hsa_circ_78624,RMVar_hsa_circ_210757,RMVar_hsa_circ_210758,RMVar_hsa_circ_354829 67705 RMVar_ID_67705 Human_SNP_ID_683255325 m1A Human chr20 - 49275852 49275852 49275852 TCCAGATAACAGAAAGTAACGTGAAGGAATTCAGGTGACTCAGACATGGAGGAGAGAAGACCTCA TCCAGATAACAGAAAGTAACGTGAAGGAATTCGGGTGACTCAGACATGGAGGAGAGAAGACCTCA T C ZNFX1 Ensembl:ENSG00000124201 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:49275784..49278045 26863196 MeRIP-seq:(Medium) rs763537360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926030,Human_RBP_ID_3650652,Human_RBP_ID_27819907 Human_Splice_Rec_2093400,Human_Splice_Rec_2093401,Human_Splice_Rec_2093432,Human_Splice_Rec_2093433,Human_Splice_Rec_2093458,Human_Splice_Rec_2093459,Human_Splice_Rec_2093484,Human_Splice_Rec_2093485 Human_miRNA_ID_2980017 RMVar_hsa_circ_110700,RMVar_hsa_circ_210759,RMVar_hsa_circ_46770,RMVar_hsa_circ_50682,RMVar_hsa_circ_363713,RMVar_hsa_circ_33853,RMVar_hsa_circ_80227,RMVar_hsa_circ_59743,RMVar_hsa_circ_210773,RMVar_hsa_circ_47315 67706 RMVar_ID_67706 Human_SNP_ID_683255838 m1A Human chr20 - 49277949 49277949 49277949 TTGCCTCGCCGCGAACCCCGGCGCCCGCGCCGACCCGCCACTGCCTCTGCCCGTAAGACCTGTCA TTGCCTCGCCGCGAACCCCGGCGCCCGCGCCGCCCCGCCACTGCCTCTGCCCGTAAGACCTGTCA T G ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:49277932..49278037 26863196 MeRIP-seq:(Medium) rs1002185967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19106771 Human_Splice_Rec_2093483 RMVar_hsa_circ_80227,RMVar_hsa_circ_210773 67707 RMVar_ID_67707 Human_SNP_ID_683256174 m1A Human chr20 + 49278700 49278700 49278700 TGGTACTTCTCCTAGTTGCAGTCAGGCTTCATACGCTATTGTCCTGCCCGTAAGTTCCCGTTTTG TGGTACTTCTCCTAGTTGCAGTCAGGCTTCATGCGCTATTGTCCTGCCCGTAAGTTCCCGTTTTG A G ZFAS1 Ensembl:ENSG00000177410 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:49278651..49278771;chr20:49278651..49278787;chr20:49278651..49278725 26863196 MeRIP-seq:(Medium) rs1216238077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565827,Human_RBP_ID_1026485,Human_RBP_ID_1598583,Human_RBP_ID_1931085,Human_RBP_ID_2687381,Human_RBP_ID_4651395,Human_RBP_ID_5100353,Human_RBP_ID_5119015,Human_RBP_ID_5596645,Human_RBP_ID_8535151,Human_RBP_ID_9117867,Human_RBP_ID_9390939,Human_RBP_ID_18422921,Human_RBP_ID_19106772,Human_RBP_ID_23908868,Human_RBP_ID_26491328,Human_RBP_ID_27486757 Human_Splice_Rec_2093511,Human_Splice_Rec_2093517,Human_Splice_Rec_2093521,Human_Splice_Rec_2093531,Human_Splice_Rec_2093547,Human_Splice_Rec_2093555,Human_Splice_Rec_2093557,Human_Splice_Rec_2093559,Human_Splice_Rec_2093565,Human_Splice_Rec_2093569 Human_miRNA_ID_3149963,Human_miRNA_ID_3186786,Human_miRNA_ID_3193914 67708 RMVar_ID_67708 Human_SNP_ID_683257311 m1A Human chr20 - 49281405 49281396 49281405 CCTATTTGGAAAAGTCCCCCTCACTCCTAGCAACCAGCTCTGTAAACAAGTTTCCTGCCCTTCCC CCTATTTGGAAAAGTCCCCCTCACTCCTAGCA_________GTAAACAAGTTTCCTGCCCTTCCC CAGAGCTGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49281402..49281502 26863196 MeRIP-seq:(Medium) rs965819390 Functional Loss DEL dbSNP153 33..41 33 - - - 67709 RMVar_ID_67709 Human_SNP_ID_683258833 m1A Human chr20 + 49286146 49286146 49286146 TATCCTTTTTACATTGTTCTATTTCATGCTGTAGGGCTTAAGTGTGTGGCTAGGGGGAACATGGG TATCCTTTTTACATTGTTCTATTTCATGCTGTGGGGCTTAAGTGTGTGGCTAGGGGGAACATGGG A G ZFAS1 Ensembl:ENSG00000177410 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:49286144..49286249 26863196 MeRIP-seq:(Medium) rs1010327883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7009269,Human_RBP_ID_14130738,Human_RBP_ID_17144294,Human_RBP_ID_18950736 RMVar_hsa_circ_81000,RMVar_hsa_circ_210780 67710 RMVar_ID_67710 Human_SNP_ID_683259013 m1A Human chr20 + 49286714 49286714 49286714 TGTCAGTATAAGCCCCATGACAGGAATCCACCATAAGCTATACGAGGTGACCATGGAATCACAGA TGTCAGTATAAGCCCCATGACAGGAATCCACCGTAAGCTATACGAGGTGACCATGGAATCACAGA A G ZFAS1 Ensembl:ENSG00000177410 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:49286673..49286805 26863196 MeRIP-seq:(Medium) rs146153305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1099860,Human_RBP_ID_2687537,Human_RBP_ID_14130780,Human_RBP_ID_17192891 RMVar_hsa_circ_81000,RMVar_hsa_circ_210780 67711 RMVar_ID_67711 Human_SNP_ID_683259217 m1A Human chr20 + 49287354 49287342 49287355 GCAGTGGGAAGAGCAGTTGCCACGAGCGAGGGAGACTTTTCCAGATAAGGAACAAATGCGGGTTA GCAGTGGGAAGAGCAGTTGCC_____________ACTTTTCCAGATAAGGAACAAATGCGGGTTA CACGAGCGAGGGAG C ZFAS1 Ensembl:ENSG00000177410 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49287350..49287441 26863196 MeRIP-seq:(Medium) rs1300657036 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_2687548,Human_RBP_ID_3657030,Human_RBP_ID_5100373,Human_RBP_ID_7009288,Human_RBP_ID_10021625,Human_RBP_ID_14130811 RMVar_hsa_circ_81000,RMVar_hsa_circ_210780 67712 RMVar_ID_67712 Human_SNP_ID_683259754 m1A Human chr20 + 49289170 49289170 49289170 CAAGGTTACTGTATACATAGCCTGAGTTTAAAAGGCTGTGCCCACTTCAAGAATGTCATTGTTAG CAAGGTTACTGTATACATAGCCTGAGTTTAAATGGCTGTGCCCACTTCAAGAATGTCATTGTTAG A T ZFAS1 Ensembl:ENSG00000177410 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:49289026..49289225 32194978 MeRIP-seq:(Medium) rs1045343222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565849,Human_RBP_ID_1026490,Human_RBP_ID_1136042,Human_RBP_ID_1380485,Human_RBP_ID_1598615,Human_RBP_ID_1931132,Human_RBP_ID_2687594,Human_RBP_ID_3650680,Human_RBP_ID_5100378,Human_RBP_ID_7009318,Human_RBP_ID_8205534,Human_RBP_ID_8260555,Human_RBP_ID_8535228,Human_RBP_ID_9117884,Human_RBP_ID_9389520,Human_RBP_ID_14130940,Human_RBP_ID_17281907,Human_RBP_ID_17395838,Human_RBP_ID_17658895,Human_RBP_ID_17973378,Human_RBP_ID_18323131,Human_RBP_ID_18774885,Human_RBP_ID_22600403,Human_RBP_ID_23908939,Human_RBP_ID_26491353,Human_RBP_ID_27702676 RMVar_hsa_circ_81000,RMVar_hsa_circ_210780 67713 RMVar_ID_67713 Human_SNP_ID_683363077 m1A Human chr20 + 49713612 49713612 49713612 GCCGGGCGCCACATAGACGAAGTACAGCAGCGAGGACGAGAGAGAAAAGAAGAAGAGCGCGGCGA GCCGGGCGCCACATAGACGAAGTACAGCAGCGTGGACGAGAGAGAAAAGAAGAAGAGCGCGGCGA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:49713579..49713779 32194978 MeRIP-seq:(Medium) rs569993024 Functional Loss SNV dbSNP153 33..33 33 - - - 67714 RMVar_ID_67714 Human_SNP_ID_683363114 m1A Human chr20 + 49713671 49713671 49713671 CGGCGAGCAGCGAGCGGCGCGGCAGCCGCAGCAGCCCCCGGCGGGCGCGCATGCTGCAGCCAGGC CGGCGAGCAGCGAGCGGCGCGGCAGCCGCAGCGGCCCCCGGCGGGCGCGCATGCTGCAGCCAGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:49713622..49713878 26863196 MeRIP-seq:(Medium) rs868063985 Functional Loss SNV dbSNP153 33..33 33 - - - 67715 RMVar_ID_67715 Human_SNP_ID_683363167 m1A Human chr20 - 49713821 49713812 49713822 CGGCTGGGAGCGGCGAGGCGGCGGCGGCGGCGAGTGGCGGCCCGCGAGGCCCGGGAGGCGGTGGC CGGCTGGGAGCGGCGAGGCGGCGGCGGCGGC__________CCGCGAGGCCCGGGAGGCGGTGGC GGCCGCCACTC G B4GALT5 Ensembl:ENSG00000158470 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:49713742..49713827;chr20:49713579..49713875;chr20:49713519..49713875 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1231869604 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_244563,Human_RBP_ID_4659459,Human_RBP_ID_9331562,Human_RBP_ID_18422922,Human_RBP_ID_22453141 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 67716 RMVar_ID_67716 Human_SNP_ID_683363170 m1A Human chr20 - 49713838 49713814 49713838 CGGCCCGCGACGGCCGGCGGCTGGGAGCGGCGAGGCGGCGGCGGCGGCGAGTGGCGGCCCGCGAG CGGCCCGCGACGGCCGGCGGCTGGGAGCGGCG________________________GCCCGCGAG CCGCCACTCGCCGCCGCCGCCGCCT C B4GALT5 Ensembl:ENSG00000158470 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49713579..49713883 26863196 MeRIP-seq:(Medium) rs1054463157 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_244563,Human_RBP_ID_926986,Human_RBP_ID_4659459,Human_RBP_ID_9331562,Human_RBP_ID_18422922,Human_RBP_ID_22453141 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 67717 RMVar_ID_67717 Human_SNP_ID_683363172 m1A Human chr20 - 49713821 49713821 49713821 CGGCTGGGAGCGGCGAGGCGGCGGCGGCGGCGAGTGGCGGCCCGCGAGGCCCGGGAGGCGGTGGC CGGCTGGGAGCGGCGAGGCGGCGGCGGCGGCGTGTGGCGGCCCGCGAGGCCCGGGAGGCGGTGGC T A B4GALT5 Ensembl:ENSG00000158470 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:49713742..49713827;chr20:49713579..49713875;chr20:49713519..49713875 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1334046800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244563,Human_RBP_ID_4659459,Human_RBP_ID_9331562,Human_RBP_ID_18422922,Human_RBP_ID_22453141 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 67718 RMVar_ID_67718 Human_SNP_ID_683389082 m1A Human chr20 - 49815082 49815082 49815082 CGGGGAGGATGGGCTTGCCAGGGGTCGGGAGCACCAGTTTCGTCGTGACAACCAGGGTGGTGTGG CGGGGAGGATGGGCTTGCCAGGGGTCGGGAGCGCCAGTTTCGTCGTGACAACCAGGGTGGTGTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49815036..49815114 26863196 MeRIP-seq:(Medium) rs1193293134 Functional Loss SNV dbSNP153 33..33 33 - - - 67719 RMVar_ID_67719 Human_SNP_ID_683408843 m1A Human chr20 + 49891028 49891026 49891028 TGAAGTCTCAGGTCCGTGTTCCCGCAGGGCGCACATGCTTGGAGAGTCCTCAGCAGGGTAGCCGA TGAAGTCTCAGGTCCGTGTTCCCGCAGGGCG__CATGCTTGGAGAGTCCTCAGCAGGGTAGCCGA GCA G SLC9A8 Ensembl:ENSG00000197818 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49890981..49891096 26863196 MeRIP-seq:(Medium) rs1031391995 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_267681,RMVar_hsa_circ_210813,RMVar_hsa_circ_103913 67720 RMVar_ID_67720 Human_SNP_ID_683413013 m1A Human chr20 - 49906537 49906537 49906537 CGCGGCTGCTCGGACGCCCTGCGGCGGCGGGCAGAGGGCCGGGAGCACCTGACGGCCTCCATGTC CGCGGCTGCTCGGACGCCCTGCGGCGGCGGGCGGAGGGCCGGGAGCACCTGACGGCCTCCATGTC T C SPATA2 Ensembl:ENSG00000158480 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:49906461..49906546 26863410 MeRIP-seq:(Medium) rs370523989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244884,Human_RBP_ID_22080709 67721 RMVar_ID_67721 Human_SNP_ID_683421242 m1A Human chr20 + 49936450 49936450 49936450 GGCGCAACAGCGGGACTGCGGGGGTGCTGCGCAGCTGGCGGGGCCGGCGGCGGAGGCTGACCCCC GGCGCAACAGCGGGACTGCGGGGGTGCTGCGCCGCTGGCGGGGCCGGCGGCGGAGGCTGACCCCC A C RNF114 Ensembl:ENSG00000124226 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:49936401..49936591;chr20:49936401..49936597;chr20:49936401..49936615;chr20:49936401..49936550 26863196 MeRIP-seq:(Medium) rs1234112847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244823,Human_RBP_ID_4659904,Human_RBP_ID_5503501,Human_RBP_ID_8855614,Human_RBP_ID_22453568 67722 RMVar_ID_67722 Human_SNP_ID_683421274 m1A Human chr20 - 49936497 49936497 49936497 CGGCTTCTCGTACACCTCTAAGCACACGGGACACGTGAAGCGTCCTAGGGGGTCAGCCTCCGCCG CGGCTTCTCGTACACCTCTAAGCACACGGGACGCGTGAAGCGTCCTAGGGGGTCAGCCTCCGCCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:49936401..49936528 26863410 MeRIP-seq:(Medium) rs1386412786 Functional Loss SNV dbSNP153 33..33 33 - - - 67723 RMVar_ID_67723 Human_SNP_ID_683421275 m1A Human chr20 - 49936499 49936499 49936499 ACCGGCTTCTCGTACACCTCTAAGCACACGGGACACGTGAAGCGTCCTAGGGGGTCAGCCTCCGC ACCGGCTTCTCGTACACCTCTAAGCACACGGGGCACGTGAAGCGTCCTAGGGGGTCAGCCTCCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:49936451..49936575 32194978 MeRIP-seq:(Medium) rs373668213 Functional Loss SNV dbSNP153 33..33 33 - - - 67724 RMVar_ID_67724 Human_SNP_ID_683434191 m1A Human chr20 - 49983020 49983020 49983020 GAGGCACTGGGGTCGCCGATTCGCGCAGCAGTAGCGCAGAAGAACCACTCGCTAGGCCGTGCCGC GAGGCACTGGGGTCGCCGATTCGCGCAGCAGTGGCGCAGAAGAACCACTCGCTAGGCCGTGCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:49983006..49983118 26863196 MeRIP-seq:(Medium) rs777300879 Functional Loss SNV dbSNP153 33..33 33 - - - 67725 RMVar_ID_67725 Human_SNP_ID_683434222 m1A Human chr20 - 49983059 49983059 49983059 GAGGGCTTCCTGACGAGGAAAGAGCGCGGCATAGTGGTCGAGGCACTGGGGTCGCCGATTCGCGC GAGGGCTTCCTGACGAGGAAAGAGCGCGGCATGGTGGTCGAGGCACTGGGGTCGCCGATTCGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:49983010..49983123 26863196 MeRIP-seq:(Medium) rs778487835 Functional Loss SNV dbSNP153 33..33 33 - - - 67726 RMVar_ID_67726 Human_SNP_ID_683460287 m1A Human chr20 - 50082752 50082752 50082752 AGTGTTACAGCAATTAATCAAAAAGAAAAACCACAGGCCCTTCCCCTTCCCCCCAATTCGATTTA AGTGTTACAGCAATTAATCAAAAAGAAAAACCGCAGGCCCTTCCCCTTCCCCCCAATTCGATTTA T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50082703..50082819 26863196 MeRIP-seq:(Medium) rs1472196388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_566153,Human_RBP_ID_17659414,Human_RBP_ID_25631216 Human_miRNA_ID_1478759,Human_miRNA_ID_1478760 67727 RMVar_ID_67727 Human_SNP_ID_683460299 m1A Human chr20 - 50082789 50082785 50082789 AAAGAAAATATGAAACTCCCTCAGCCGCCCGAAGGACAGTGTTACAGCAATTAATCAAAAAGAAA AAAGAAAATATGAAACTCCCTCAGCCGCCCGA____CAGTGTTACAGCAATTAATCAAAAAGAAA GTCCT G TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50082738..50082818 26863196 MeRIP-seq:(Medium) rs1336535634 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_566154,Human_RBP_ID_779514,Human_RBP_ID_7010327,Human_RBP_ID_14134070,Human_RBP_ID_17973590,Human_RBP_ID_26343751 67728 RMVar_ID_67728 Human_SNP_ID_683465356 m1A Human chr20 - 50102683 50102683 50102683 TAGTTTACCTTTAAGAGGATCGTCGGCCGAGCACGGTGGCTCACACCTGTAATCCCAGCACTTTG TAGTTTACCTTTAAGAGGATCGTCGGCCGAGCTCGGTGGCTCACACCTGTAATCCCAGCACTTTG T A TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50102680..50103048 26863196 MeRIP-seq:(Medium) rs992990379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149299,Human_RBP_ID_14134795 RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 67729 RMVar_ID_67729 Human_SNP_ID_683465357 m1A Human chr20 - 50102683 50102683 50102683 TAGTTTACCTTTAAGAGGATCGTCGGCCGAGCACGGTGGCTCACACCTGTAATCCCAGCACTTTG TAGTTTACCTTTAAGAGGATCGTCGGCCGAGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTG T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50102680..50103048 26863196 MeRIP-seq:(Medium) rs992990379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149299,Human_RBP_ID_14134795 RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 67730 RMVar_ID_67730 Human_SNP_ID_683468029 m1A Human chr20 - 50113119 50113119 50113119 CCTTCAAGCAAGAGCGACGCAAGATGGCAGCCACCACGGGCTCGGGTGAGCGGGGGCGCCGGGCC CCTTCAAGCAAGAGCGACGCAAGATGGCAGCCGCCACGGGCTCGGGTGAGCGGGGGCGCCGGGCC T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:50112989..50113118 26863196 MeRIP-seq:(Medium) rs754286855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831704,Human_RBP_ID_18423159,Human_RBP_ID_19108839,Human_RBP_ID_22452797,Human_RBP_ID_26343110 Human_Splice_Rec_2093827,Human_Splice_Rec_2093831,Human_Splice_Rec_2093837,Human_Splice_Rec_2093841,Human_Splice_Rec_2093847,Human_Splice_Rec_2093855,Human_Splice_Rec_2093893,Human_Splice_Rec_2093899,Human_Splice_Rec_2093905,Human_Splice_Rec_2093907,Human_Splice_Rec_2093911,Human_Splice_Rec_2093917,Human_Splice_Rec_2093923,Human_Splice_Rec_2093929,Human_Splice_Rec_2093933 RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 67731 RMVar_ID_67731 Human_SNP_ID_683475782 m1A Human chr20 + 50143594 50143594 50143594 GGTTGTGGGCGATGAGGCTGAAGCACAGGATCACAGAGCACCACTCCTGGAGGCGCTTGCCTGCA GGTTGTGGGCGATGAGGCTGAAGCACAGGATCGCAGAGCACCACTCCTGGAGGCGCTTGCCTGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:50143544..50153588 32194978 MeRIP-seq:(Medium) rs1293310672 Functional Loss SNV dbSNP153 33..33 33 - - - 67732 RMVar_ID_67732 Human_SNP_ID_683478274 m1A Human chr20 - 50153518 50153518 50153518 GGGGCCCGCGAGCTGGCTGCGCTCTACTCGCCAGGTAAGACCTCTGGGCCCCCCTCCAGGCCTGC GGGGCCCGCGAGCTGGCTGCGCTCTACTCGCCGGGTAAGACCTCTGGGCCCCCCTCCAGGCCTGC T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:50153501..50153700 26863196 MeRIP-seq:(Medium) rs112531057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660515,Human_RBP_ID_19108843,Human_RBP_ID_22453572 Human_Splice_Rec_2093947,Human_Splice_Rec_2093961,Human_Splice_Rec_2093971,Human_Splice_Rec_2093989,Human_Splice_Rec_2094001 67733 RMVar_ID_67733 Human_SNP_ID_683478332 m1A Human chr20 - 50153622 50153622 50153622 CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGAACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGTACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG T A TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:50153526..50153684 26863196 MeRIP-seq:(Medium) rs232733 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_779577,Human_RBP_ID_4659469,Human_RBP_ID_9331567,Human_RBP_ID_18422924,Human_RBP_ID_22453144,Human_RBP_ID_26491557 67734 RMVar_ID_67734 Human_SNP_ID_683478333 m1A Human chr20 - 50153622 50153622 50153622 CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGAACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGGACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:50153526..50153684 26863196 MeRIP-seq:(Medium) rs232733 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_779577,Human_RBP_ID_4659469,Human_RBP_ID_9331567,Human_RBP_ID_18422924,Human_RBP_ID_22453144,Human_RBP_ID_26491557 67735 RMVar_ID_67735 Human_SNP_ID_683478334 m1A Human chr20 - 50153622 50153622 50153622 CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGAACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGCACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG T G TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:50153526..50153684 26863196 MeRIP-seq:(Medium) rs232733 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_779577,Human_RBP_ID_4659469,Human_RBP_ID_9331567,Human_RBP_ID_18422924,Human_RBP_ID_22453144,Human_RBP_ID_26491557 67736 RMVar_ID_67736 Human_SNP_ID_683478386 m1A Human chr20 - 50153671 50153671 50153671 CGCGGTTCCGCGGCCCTGCCGCCGCCGCCGCCAGCAGAGCGCACCGGGCCGATCGGGCGAGTGGC CGCGGTTCCGCGGCCCTGCCGCCGCCGCCGCCCGCAGAGCGCACCGGGCCGATCGGGCGAGTGGC T G TMEM189 Ensembl:ENSG00000240849 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50153526..50153725 26863196 MeRIP-seq:(Medium) rs1480104161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659470,Human_RBP_ID_9331913,Human_RBP_ID_18422924,Human_RBP_ID_22453572 67737 RMVar_ID_67737 Human_SNP_ID_683488197 m1A Human chr20 + 50191218 50191218 50191218 GGCCAGACCCGGGCCGCGCCCCCCCGCCGGCGAGCTGGGCAGCATCGGCGACCACGAGCGCGCCA GGCCAGACCCGGGCCGCGCCCCCCCGCCGGCGGGCTGGGCAGCATCGGCGACCACGAGCGCGCCA A G CEBPB Ensembl:ENSG00000172216 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:50191124..50191321 32194978 MeRIP-seq:(Medium) rs1436941998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8857529 67738 RMVar_ID_67738 Human_SNP_ID_683488203 m1A Human chr20 + 50191226 50191226 50191226 CCGGGCCGCGCCCCCCCGCCGGCGAGCTGGGCAGCATCGGCGACCACGAGCGCGCCATCGACTTC CCGGGCCGCGCCCCCCCGCCGGCGAGCTGGGCCGCATCGGCGACCACGAGCGCGCCATCGACTTC A C CEBPB Ensembl:ENSG00000172216 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:50191201..50191225 26863196 MeRIP-seq:(Medium) rs1456605960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8857529 67739 RMVar_ID_67739 Human_SNP_ID_683488210 m1A Human chr20 + 50191250 50191250 50191250 AGCTGGGCAGCATCGGCGACCACGAGCGCGCCATCGACTTCAGCCCGTACCTGGAGCCGCTGGGC AGCTGGGCAGCATCGGCGACCACGAGCGCGCCCTCGACTTCAGCCCGTACCTGGAGCCGCTGGGC A C CEBPB Ensembl:ENSG00000172216 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:50191201..50191425 26863196 MeRIP-seq:(Medium) rs1255238207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22453574 67740 RMVar_ID_67740 Human_SNP_ID_683488263 m1A Human chr20 + 50191377 50191377 50191377 CGCCCCCGCGCCCGCCTCCTCCGGGCAGCACCACGACTTCCTCTCCGACCTCTTCTCCGACGACT CGCCCCCGCGCCCGCCTCCTCCGGGCAGCACCGCGACTTCCTCTCCGACCTCTTCTCCGACGACT A G CEBPB Ensembl:ENSG00000172216 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:50191124..50191418 26863196 MeRIP-seq:(Medium) rs1364075169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4652096,Human_RBP_ID_5503515,Human_RBP_ID_27486951 67741 RMVar_ID_67741 Human_SNP_ID_683488463 m1A Human chr20 - 50191802 50191766 50191802 CACGGTCTTCTTGGCCTTGCTCTTGACCTGCGAGGGCGCCGGCGCGGCCCCCGCGTAGCAGGCGG CACGGTCTTCTTGGCCTTGCTCTTGACCTGCG_________________________________ CCGACCGCCTGCTACGCGGGGGCCGCGCCGGCGCCCT C CEBPB-AS1 RNACentral:URS00007E368D lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr20:50191737..50191867;chr20:50191564..50191858 26863196,26863410 MeRIP-seq:(Medium) rs781132105 Functional Loss DEL dbSNP153 33..65 33 - - - 67742 RMVar_ID_67742 Human_SNP_ID_683488499 m1A Human chr20 + 50191838 50191838 50191838 AGGTCAAGAGCAAGGCCAAGAAGACCGTGGACAAGCACAGCGACGAGTACAAGATCCGGCGCGAG AGGTCAAGAGCAAGGCCAAGAAGACCGTGGACCAGCACAGCGACGAGTACAAGATCCGGCGCGAG A C CEBPB Ensembl:ENSG00000172216 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:50191265..50191934 26863196 MeRIP-seq:(Medium) rs1568674270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780018,Human_RBP_ID_1598832,Human_RBP_ID_5595205,Human_RBP_ID_14135414,Human_RBP_ID_27486964 67743 RMVar_ID_67743 Human_SNP_ID_683515518 m1A Human chr20 - 50300925 50300925 50300925 ACTCATGGAATCACCAATCCATCTACCCATTTATCCCTTTATCTGTTTATTCATCTAGCCATCTA ACTCATGGAATCACCAATCCATCTACCCATTTGTCCCTTTATCTGTTTATTCATCTAGCCATCTA T C LINC01271,LINC01271:2,LINC01271:3 RNACentral:URS00008BD331,RNACentral:URS0000D5CE13,RNACentral:URS0000D5700B lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50300874..50301045 26863196 MeRIP-seq:(Medium) rs542250505 Functional Loss SNV dbSNP153 33..33 33 - - - 67744 RMVar_ID_67744 Human_SNP_ID_683515665 m1A Human chr20 - 50301346 50301219 50301347 ATCCATCCATCTATTCTCTTATCCACCCTCCTACCCACCAATCTATTCATTTATCTACCCATCCA ATCCATCCATCTATTCTCTTATCCACCCTCC__________________________________ GGGAGGGTGGATAATAGAATAGATGGATGGGTAGGTGGATAGATGGATGGGTAGGTGGATAGATGGATGGATGAGTGGGTGGACGGATAGGCGAATGGATGGGTAGATAAATGAATAGATTGGTGGGTA G LINC01271,LINC01271:2,LINC01271:3 RNACentral:URS00008BD331,RNACentral:URS0000D5CE13,RNACentral:URS0000D5700B lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50301116..50301524 26863196 MeRIP-seq:(Medium) rs1568708596 Functional Loss DEL dbSNP153 32..65 33 - - - 67745 RMVar_ID_67745 Human_SNP_ID_683515769 m1A Human chr20 - 50301402 50301402 50301402 ATTCATCCACCAATCAATCTAACCATCCATCCATCTTTCCATCCATCCATCCACCTATCCATCCA ATTCATCCACCAATCAATCTAACCATCCATCCGTCTTTCCATCCATCCATCCACCTATCCATCCA T C LINC01271,LINC01271:2,LINC01271:3 RNACentral:URS00008BD331,RNACentral:URS0000D5CE13,RNACentral:URS0000D5700B lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:50301257..50301499 26863196 MeRIP-seq:(Medium) rs1316285791 Functional Loss SNV dbSNP153 33..33 33 - - - 67746 RMVar_ID_67746 Human_SNP_ID_683517771 m1A Human chr20 + 50309800 50309800 50309800 CTCTGATGGGGTGACATTTGAACAGAAGCCCCAACAAAGAGGAGAAGCCCACGTGCAAAGGCAGG CTCTGATGGGGTGACATTTGAACAGAAGCCCCGACAAAGAGGAGAAGCCCACGTGCAAAGGCAGG A G LINC01270 Ensembl:ENSG00000203999 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50309787..50309872 26863196 MeRIP-seq:(Medium) rs1313835340 Functional Loss SNV dbSNP153 33..33 33 - - - 67747 RMVar_ID_67747 Human_SNP_ID_683518387 m1A Human chr20 + 50312239 50312239 50312239 ATGGCCGGCTCATTCTCATCTTTCTTGGCTCAAATGTTACCTCCCCAACCTAGACAGCACCGCTG ATGGCCGGCTCATTCTCATCTTTCTTGGCTCAGATGTTACCTCCCCAACCTAGACAGCACCGCTG A G LINC01270 Ensembl:ENSG00000203999 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50312130..50312301 26863196 MeRIP-seq:(Medium) rs1181332687 Functional Loss SNV dbSNP153 33..33 33 - - - 67748 RMVar_ID_67748 Human_SNP_ID_683520492 m1A Human chr20 - 50321015 50321005 50321016 GGGTAATGGGTGCTCCAGGAAACCAGAACGGCAGATGCGAGGTTCTGAGGTGGAGCCTGGAGTGT GGGTAATGGGTGCTCCAGGAAACCAGAACGG___________TTCTGAGGTGGAGCCTGGAGTGT ACCTCGCATCTG A LINC01271 Ensembl:ENSG00000233077 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:50320964..50321035 26863196 MeRIP-seq:(Medium) rs1202900618 Functional Loss DEL dbSNP153 32..42 33 - - - 67749 RMVar_ID_67749 Human_SNP_ID_683568118 m1A Human chr20 + 50510480 50510480 50510480 GGCTAAGAGCGCGACGCGGCCTAGAGCGGCAGACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAG GGCTAAGAGCGCGACGCGGCCTAGAGCGGCAGCCGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAG A C PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:50510434..50510576 26863196 MeRIP-seq:(Medium) rs750024069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924609,Human_RBP_ID_4652154,Human_RBP_ID_9298514,Human_RBP_ID_18423162,Human_RBP_ID_22080732,Human_RBP_ID_26343111 67750 RMVar_ID_67750 Human_SNP_ID_683568119 m1A Human chr20 + 50510480 50510480 50510480 GGCTAAGAGCGCGACGCGGCCTAGAGCGGCAGACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAG GGCTAAGAGCGCGACGCGGCCTAGAGCGGCAGGCGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAG A G PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:50510434..50510576 26863196 MeRIP-seq:(Medium) rs750024069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924609,Human_RBP_ID_4652154,Human_RBP_ID_9298514,Human_RBP_ID_18423162,Human_RBP_ID_22080732,Human_RBP_ID_26343111 67751 RMVar_ID_67751 Human_SNP_ID_683568135 m1A Human chr20 + 50510511 50510511 50510511 GACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAGCCGCCCTGGCCCGTCATGGAGATGGAAAAGG GACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCCGCCGCCCTGGCCCGTCATGGAGATGGAAAAGG A C PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:50510429..50510522 26863410 MeRIP-seq:(Medium) rs1296161423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924609,Human_RBP_ID_4659910,Human_RBP_ID_7010774,Human_RBP_ID_9390951,Human_RBP_ID_17973690,Human_RBP_ID_22600434,Human_RBP_ID_26343112 Human_Splice_Rec_2094217,Human_Splice_Rec_2094233 67752 RMVar_ID_67752 Human_SNP_ID_683568136 m1A Human chr20 + 50510511 50510511 50510511 GACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCAGCCGCCCTGGCCCGTCATGGAGATGGAAAAGG GACGGCGCAGTGGGCCGAGAAGGAGGCGCAGCGGCCGCCCTGGCCCGTCATGGAGATGGAAAAGG A G PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:50510429..50510522 26863410 MeRIP-seq:(Medium) rs1296161423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924609,Human_RBP_ID_4659910,Human_RBP_ID_7010774,Human_RBP_ID_9390951,Human_RBP_ID_17973690,Human_RBP_ID_22600434,Human_RBP_ID_26343112 Human_Splice_Rec_2094217,Human_Splice_Rec_2094233 67753 RMVar_ID_67753 Human_SNP_ID_683568149 m1A Human chr20 + 50510528 50510528 50510528 AGAAGGAGGCGCAGCAGCCGCCCTGGCCCGTCATGGAGATGGAAAAGGAGTTCGAGCAGATCGAC AGAAGGAGGCGCAGCAGCCGCCCTGGCCCGTCGTGGAGATGGAAAAGGAGTTCGAGCAGATCGAC A G PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:50510423..50510559 26863196 MeRIP-seq:(Medium) rs147498342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4652157,Human_RBP_ID_7010774,Human_RBP_ID_9389525,Human_RBP_ID_17973690,Human_RBP_ID_26343112,Human_RBP_ID_27820408 Human_Splice_Rec_2094217,Human_Splice_Rec_2094233 67754 RMVar_ID_67754 Human_SNP_ID_683568150 m1A Human chr20 + 50510532 50510532 50510532 GGAGGCGCAGCAGCCGCCCTGGCCCGTCATGGAGATGGAAAAGGAGTTCGAGCAGATCGACAAGT GGAGGCGCAGCAGCCGCCCTGGCCCGTCATGGTGATGGAAAAGGAGTTCGAGCAGATCGACAAGT A T PTPN1 Ensembl:ENSG00000196396 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:50510376..50561400;chr20:50510376..50561402 26863196 MeRIP-seq:(Medium) rs1407157199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1598858,Human_RBP_ID_3650983,Human_RBP_ID_4652157,Human_RBP_ID_7010775,Human_RBP_ID_9389525,Human_RBP_ID_17973690,Human_RBP_ID_26343112,Human_RBP_ID_27820408 Human_Splice_Rec_2094217,Human_Splice_Rec_2094233 67755 RMVar_ID_67755 Human_SNP_ID_683584178 m1A Human chr20 - 50579808 50579808 50579808 CACCCACTGGTGATTTGGGAAGAACTCCCTGCATTTCCCATTGTGTGGCTCCAGGATTCGTTTGG CACCCACTGGTGATTTGGGAAGAACTCCCTGCGTTTCCCATTGTGTGGCTCCAGGATTCGTTTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50579759..50579849 26863196 MeRIP-seq:(Medium) rs762671904 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 67756 RMVar_ID_67756 Human_SNP_ID_683584580 m1A Human chr20 - 50581254 50581254 50581254 AACTTCAGTGTCTTGACTCATGCTGAGGAATCAGAGGGCAGAGATGGGTTACTCACTTTGGAGAA AACTTCAGTGTCTTGACTCATGCTGAGGAATCGGAGGGCAGAGATGGGTTACTCACTTTGGAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:50581251..50581375 26863196 MeRIP-seq:(Medium) rs371265377 Functional Loss SNV dbSNP153 33..33 33 - - - 67757 RMVar_ID_67757 Human_SNP_ID_683626995 m1A Human chr20 + 50739914 50739914 50739914 GGAGAAGGCAGTGGCGGGAAGGTAGGAGGGGAAATACTTGGGAGTCATTGCACTCACTGTGGCTG GGAGAAGGCAGTGGCGGGAAGGTAGGAGGGGAGATACTTGGGAGTCATTGCACTCACTGTGGCTG A G PARD6B Ensembl:ENSG00000124171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50739798..50739937 26863196 MeRIP-seq:(Medium) rs1235920272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832271,Human_RBP_ID_8234816,Human_RBP_ID_9431314 RMVar_hsa_circ_82913,RMVar_hsa_circ_210842 67758 RMVar_ID_67758 Human_SNP_ID_683653514 m1A Human chr20 - 50841889 50841889 50841889 TTCTCGGGGCAGGATACTCACGTTCCTGAAGGAGGGGAGCCCTGCGGATCCCAGCCACCTCCGCA TTCTCGGGGCAGGATACTCACGTTCCTGAAGGTGGGGAGCCCTGCGGATCCCAGCCACCTCCGCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:50841776..50841925 32194978 MeRIP-seq:(Medium) rs2145692 Functional Loss SNV dbSNP153 33..33 33 - - - 67759 RMVar_ID_67759 Human_SNP_ID_683653515 m1A Human chr20 - 50841889 50841889 50841890 TTCTCGGGGCAGGATACTCACGTTCCTGAAGGAGGGGAGCCCTGCGGATCCCAGCCACCTCCGCA TTCTCGGGGCAGGATACTCACGTTCCTGAAGTTGGGGAGCCCTGCGGATCCCAGCCACCTCCGCA TC AA - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:50841776..50841925 32194978 MeRIP-seq:(Medium) rs375476882 Functional Loss MNV dbSNP153 32..33 33 - - - 67760 RMVar_ID_67760 Human_SNP_ID_683662460 m1A Human chr20 - 50877052 50877051 50877053 GGCAGAGCACACCCCGTGCAAAAACCCATCACAGAGAGAAGGACCATGGAGCCCCTGCAAAGCCA GGCAGAGCACACCCCGTGCAAAAACCCATCA__GAGAGAAGGACCATGGAGCCCCTGCAAAGCCA CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50877015..50877091 26863196 MeRIP-seq:(Medium) rs1362245965 Functional Loss DEL dbSNP153 32..33 33 - - - 67761 RMVar_ID_67761 Human_SNP_ID_683666394 m1A Human chr20 + 50891826 50891823 50891826 TCTCAGATGGAGAAGCACCGTCTTTCCACTCAACAACATCGTCTTGGTCAACCTCACTATCAGAT TCTCAGATGGAGAAGCACCGTCTTTCCACT___CAACATCGTCTTGGTCAACCTCACTATCAGAT TCAA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:50891776..50891850 26863196 MeRIP-seq:(Medium) rs750133102 Functional Loss DEL dbSNP153 31..33 33 - - - 67762 RMVar_ID_67762 Human_SNP_ID_683677515 m1A Human chr20 - 50928820 50928810 50928820 ATTTTACTCCTCTTGTTATTTCCATAGGTGTGAGATGCACAATGCGAAACCTAGGCCCCAGCTTT ATTTTACTCCTCTTGTTATTTCCATAGGTGTG__________TGCGAAACCTAGGCCCCAGCTTT ATTGTGCATCT A ADNP Ensembl:ENSG00000101126 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:50928751..50928874 26863196 MeRIP-seq:(Medium) rs1321983627 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_25619993 Human_Splice_Rec_2094456,Human_Splice_Rec_2094466,Human_Splice_Rec_2094482 Human_miRNA_ID_2451186 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052,RMVar_hsa_circ_210856,RMVar_hsa_circ_332419 67763 RMVar_ID_67763 Human_SNP_ID_683678202 m1A Human chr20 - 50930592 50930592 50930592 TCTGCTCCGGAGGTCCAGGCGCCTCCTCCTGCAGCCCGACCCCCTTCTCCGCCCTGTGAGCCCAC TCTGCTCCGGAGGTCCAGGCGCCTCCTCCTGCCGCCCGACCCCCTTCTCCGCCCTGTGAGCCCAC T G ADNP Ensembl:ENSG00000101126 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50930586..50930734 26863196 MeRIP-seq:(Medium) rs1436375404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132551,Human_RBP_ID_17086104,Human_RBP_ID_17396639,Human_RBP_ID_26787954 RMVar_hsa_circ_94612,RMVar_hsa_circ_210846 67764 RMVar_ID_67764 Human_SNP_ID_683678356 m1A Human chr20 - 50930864 50930849 50930864 CGCCCGCCGCCGCCGCCGCTGTCCGGCCCCCGAGCACGCCGGCCCCGCGCGCGCCTCGAGGCCGA CGCCCGCCGCCGCCGCCGCTGTCCGGCCCCCG_______________CGCGCGCCTCGAGGCCGA GCGGGGCCGGCGTGCT G ADNP Ensembl:ENSG00000101126 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:50930776..50931141 26863196 MeRIP-seq:(Medium) rs1048845160 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_832041,Human_RBP_ID_9331580,Human_RBP_ID_17396640,Human_RBP_ID_18495176,Human_RBP_ID_19106797,Human_RBP_ID_22533650 Human_Splice_Rec_2094455,Human_Splice_Rec_2094465,Human_Splice_Rec_2094481,Human_Splice_Rec_2094489,Human_Splice_Rec_2094501 RMVar_hsa_circ_94612,RMVar_hsa_circ_210846 67765 RMVar_ID_67765 Human_SNP_ID_683678379 m1A Human chr20 + 50930898 50930882 50930899 GGGGGCCGGACAGCGGCGGCGGCGGCGGGCGGATGGCGGCGGCACGGCGGTGGCGGCAGCGGGGA GGGGGCCGGACAGCGGC_________________GGCGGCGGCACGGCGGTGGCGGCAGCGGGGA CGGCGGCGGCGGGCGGAT C ADNP-AS1,ADNP-AS1:2,ADNP-AS1:3,ADNP-AS1:4 RNACentral:URS00009C1B38,RNACentral:URS0000D59F2F,RNACentral:URS0000D56DC1,RNACentral:URS0000D5D043 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:50930779..50931337;chr20:50930785..50931202;chr20:50928712..50931425 26863196 MeRIP-seq:(Medium) rs1162053488 Functional Loss DEL dbSNP153 18..34 33 - - - 67766 RMVar_ID_67766 Human_SNP_ID_683678382 m1A Human chr20 + 50930898 50930885 50930899 GGGGGCCGGACAGCGGCGGCGGCGGCGGGCGGATGGCGGCGGCACGGCGGTGGCGGCAGCGGGGA GGGGGCCGGACAGCGGCGGC______________GGCGGCGGCACGGCGGTGGCGGCAGCGGGGA CGGCGGCGGGCGGAT C ADNP-AS1,ADNP-AS1:2,ADNP-AS1:3,ADNP-AS1:4 RNACentral:URS00009C1B38,RNACentral:URS0000D59F2F,RNACentral:URS0000D56DC1,RNACentral:URS0000D5D043 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:50930779..50931337;chr20:50930785..50931202;chr20:50928712..50931425 26863196 MeRIP-seq:(Medium) rs1414456949 Functional Loss DEL dbSNP153 21..34 33 - - - 67767 RMVar_ID_67767 Human_SNP_ID_683678513 m1A Human chr20 + 50931165 50931163 50931165 GCGCTCCTCTCGCTCCTCAGCAGCGGGGACCGAGAGAGGGAGCTGTGTCTGAGAAGACGCCAAAA GCGCTCCTCTCGCTCCTCAGCAGCGGGGACC__GAGAGGGAGCTGTGTCTGAGAAGACGCCAAAA CGA C ADNP-AS1 Ensembl:ENSG00000259456 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:50930971..50931190 32194978 MeRIP-seq:(Medium) rs1186050813 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5596929 67768 RMVar_ID_67768 Human_SNP_ID_683678635 m1A Human chr20 + 50931319 50931319 50931319 GGCGGGCGGCGGAGGGGAGACCGGGCCGGCGGAGGCGGCGGCGGCAACGGGCGGGGGAGGGGGCT GGCGGGCGGCGGAGGGGAGACCGGGCCGGCGGCGGCGGCGGCGGCAACGGGCGGGGGAGGGGGCT A C ADNP-AS1 Ensembl:ENSG00000259456 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:50928790..50931425 26863410 MeRIP-seq:(Medium) rs1415408072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8205625 67769 RMVar_ID_67769 Human_SNP_ID_683678636 m1A Human chr20 + 50931319 50931319 50931319 GGCGGGCGGCGGAGGGGAGACCGGGCCGGCGGAGGCGGCGGCGGCAACGGGCGGGGGAGGGGGCT GGCGGGCGGCGGAGGGGAGACCGGGCCGGCGGGGGCGGCGGCGGCAACGGGCGGGGGAGGGGGCT A G ADNP-AS1 Ensembl:ENSG00000259456 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:50928790..50931425 26863410 MeRIP-seq:(Medium) rs1415408072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8205625 67770 RMVar_ID_67770 Human_SNP_ID_683679025 m1A Human chr20 - 50932092 50932090 50932092 GGCGGACCTTAATAAAATCTCGGCCCCTCTGCACCGAATACCCCACCAGGAAGGGCTAAGGCATC GGCGGACCTTAATAAAATCTCGGCCCCTCTGC__CGAATACCCCACCAGGAAGGGCTAAGGCATC GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:50932041..50932168 26863196 MeRIP-seq:(Medium) rs1449244232 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14139133 67771 RMVar_ID_67771 Human_SNP_ID_683682385 m1A Human chr20 - 50944410 50944410 50944410 CATCTGCTGCTCATCCTTCAATCTCTGCGTAAAGTCACCTTAGACCTTTTTTGGTTATATCTCCA CATCTGCTGCTCATCCTTCAATCTCTGCGTAAGGTCACCTTAGACCTTTTTTGGTTATATCTCCA T C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50944408..50944556 26863196 MeRIP-seq:(Medium) rs1393206639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20667081 RMVar_hsa_circ_210863,RMVar_hsa_circ_327422,RMVar_hsa_circ_375226,RMVar_hsa_circ_310353,RMVar_hsa_circ_210864,RMVar_hsa_circ_210862,RMVar_hsa_circ_210865,RMVar_hsa_circ_293392,RMVar_hsa_circ_359600 67772 RMVar_ID_67772 Human_SNP_ID_683685795 m1A Human chr20 + 50958461 50958461 50958461 GGTAAAAGCACCGAATATTTGTTCTGTCGTGGACTGCGCACTTCCAGCTCCCGCCGAGACCTGCG GGTAAAAGCACCGAATATTTGTTCTGTCGTGGGCTGCGCACTTCCAGCTCCCGCCGAGACCTGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50958410..50958525 26863196 MeRIP-seq:(Medium) rs747972169 Functional Loss SNV dbSNP153 33..33 33 - - - 67773 RMVar_ID_67773 Human_SNP_ID_683685796 m1A Human chr20 + 50958461 50958461 50958461 GGTAAAAGCACCGAATATTTGTTCTGTCGTGGACTGCGCACTTCCAGCTCCCGCCGAGACCTGCG GGTAAAAGCACCGAATATTTGTTCTGTCGTGGTCTGCGCACTTCCAGCTCCCGCCGAGACCTGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:50958410..50958525 26863196 MeRIP-seq:(Medium) rs747972169 Functional Loss SNV dbSNP153 33..33 33 - - - 67774 RMVar_ID_67774 Human_SNP_ID_683685813 m1A Human chr20 - 50958477 50958477 50958477 AGTCAGTCGTAGTCCTCGCAGGTCTCGGCGGGAGCTGGAAGTGCGCAGTCCACGACAGAACAAAT AGTCAGTCGTAGTCCTCGCAGGTCTCGGCGGGGGCTGGAAGTGCGCAGTCCACGACAGAACAAAT T C DPM1 Ensembl:ENSG00000000419 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:50958401..50958525 26863196 MeRIP-seq:(Medium) rs764346012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_566459,Human_RBP_ID_4659913,Human_RBP_ID_9118113,Human_RBP_ID_18422927,Human_RBP_ID_22453145,Human_RBP_ID_23133805,Human_RBP_ID_27022790 67775 RMVar_ID_67775 Human_SNP_ID_683698321 m1A Human chr20 - 51004703 51004703 51004703 GTTCCTCCTGCGGCTCATTCAGGCGCCCAGCAAGTTCGCCTTCCTGCGGAGCCCGCTGACGCTGA GTTCCTCCTGCGGCTCATTCAGGCGCCCAGCACGTTCGCCTTCCTGCGGAGCCCGCTGACGCTGA T G KCNG1 Ensembl:ENSG00000026559 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:51004652..51004803 32194978 MeRIP-seq:(Medium) rs761609907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22259602 67776 RMVar_ID_67776 Human_SNP_ID_683699628 m1A Human chr20 + 51009773 51009773 51009773 CCGGGCCCTCGCTGTCGCGGCCCTCGCTGTCCAGCGCGTCGTCCTCTTCCTCCCGCTCCACCATC CCGGGCCCTCGCTGTCGCGGCCCTCGCTGTCCGGCGCGTCGTCCTCTTCCTCCCGCTCCACCATC A G AL050404.1 Ensembl:ENSG00000232358 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51009723..51009823 26863196 MeRIP-seq:(Medium) rs561547195 Functional Loss SNV dbSNP153 33..33 33 - - - 67777 RMVar_ID_67777 Human_SNP_ID_683699720 m1A Human chr20 - 51010080 51010080 51010080 TGCCCTGGACCACGCTGGACGAGTTCCCGCTGACGCGCCTGGGCCAGCTCAAGGCCTGCACCAAC TGCCCTGGACCACGCTGGACGAGTTCCCGCTGGCGCGCCTGGGCCAGCTCAAGGCCTGCACCAAC T C KCNG1 Ensembl:ENSG00000026559 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr20:51010030..51010131;chr20:51010030..51010141 32194978 MeRIP-seq:(Medium) rs1486075250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210869,RMVar_hsa_circ_308202,RMVar_hsa_circ_321108 67778 RMVar_ID_67778 Human_SNP_ID_683702720 m1A Human chr20 - 51022882 51022882 51022882 GGCCGGGCCAACTCCGAGGCGGGGACGCCGCGACGGGAACTTGAGGTGGGAACTTTGCGCGCTGC GGCCGGGCCAACTCCGAGGCGGGGACGCCGCGGCGGGAACTTGAGGTGGGAACTTTGCGCGCTGC T C KCNG1 Ensembl:ENSG00000026559 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr20:51022869..51023101;chr20:51022879..51023029 26863196,32194978 MeRIP-seq:(Medium) rs1386711792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2094627,Human_Splice_Rec_2094633,Human_Splice_Rec_2094637 67779 RMVar_ID_67779 Human_SNP_ID_683702773 m1A Human chr20 - 51023053 51023053 51023053 CGGGAGGCAGAGACGGGGCGGCCGTGGCTCCGAGGGCGGGAGCTGAGCCGGGCCCCGGGACCGAA CGGGAGGCAGAGACGGGGCGGCCGTGGCTCCGGGGGCGGGAGCTGAGCCGGGCCCCGGGACCGAA T C KCNG1 Ensembl:ENSG00000026559 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51022895..51023080 26863196 MeRIP-seq:(Medium) rs992469204 Functional Loss SNV dbSNP153 33..33 33 - - - 67780 RMVar_ID_67780 Human_SNP_ID_683782594 m1A Human chr20 - 51357484 51357475 51357485 CGAAGAAGGATAAAGCACTTTAGGGAAAGAGCAGGGGTTAGTGAAGTGGGGTCTCAGTGAGCAGA CGAAGAAGGATAAAGCACTTTAGGGAAAGAG__________TGAAGTGGGGTCTCAGTGAGCAGA ACTAACCCCTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:51357469..51357541 26863196 MeRIP-seq:(Medium) rs1044407782 Functional Loss DEL dbSNP153 32..41 33 - - - 67781 RMVar_ID_67781 Human_SNP_ID_683783684 m1A Human chr20 - 51361389 51361389 51361389 GACAGAGGTGTGTGTGTGTCTGTGTGGAAGAGAGAGAGACAGAGAGACTAGTGTGTGTGTTTGTG GACAGAGGTGTGTGTGTGTCTGTGTGGAAGAGGGAGAGACAGAGAGACTAGTGTGTGTGTTTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51361268..51361561 26863196 MeRIP-seq:(Medium) rs1250208090 Functional Loss SNV dbSNP153 33..33 33 - - - 67782 RMVar_ID_67782 Human_SNP_ID_683783693 m1A Human chr20 - 51361420 51361419 51361421 GAGATTAGTGTGTGTGTGGAAGAGACAGAGAGACAGAGGTGTGTGTGTGTCTGTGTGGAAGAGAG GAGATTAGTGTGTGTGTGGAAGAGACAGAGA__CAGAGGTGTGTGTGTGTCTGTGTGGAAGAGAG GTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:51361212..51361570 26863196 MeRIP-seq:(Medium) rs1395694259 Functional Loss DEL dbSNP153 32..33 33 - - - 67783 RMVar_ID_67783 Human_SNP_ID_683802872 m1A Human chr20 - 51432669 51432669 51432669 CCCCACCCATGGAGGCCTGGGGAGCCAGCCTTACTACCCCCAGCACCCGATGGTGGCCGAGTCCC CCCCACCCATGGAGGCCTGGGGAGCCAGCCTTCCTACCCCCAGCACCCGATGGTGGCCGAGTCCC T G NFATC2 Ensembl:ENSG00000101096 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:51432620..51432701 26863196 MeRIP-seq:(Medium) rs1323369653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9389540 Human_Splice_Rec_2094666,Human_Splice_Rec_2094684,Human_Splice_Rec_2094704,Human_Splice_Rec_2094722,Human_Splice_Rec_2094742,Human_Splice_Rec_2094762 Human_miRNA_ID_1359075 RMVar_hsa_circ_356160,RMVar_hsa_circ_356825,RMVar_hsa_circ_288856 67784 RMVar_ID_67784 Human_SNP_ID_683822581 m1A Human chr20 + 51509027 51509027 51509027 AAACATGTGCGAGGCCCACGATCCGCCCCCCTATCCTTCCCCTTCCCCTGCCCTTCCCACACAGG AAACATGTGCGAGGCCCACGATCCGCCCCCCTGTCCTTCCCCTTCCCCTGCCCTTCCCACACAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51509007..51509235 26863196 MeRIP-seq:(Medium) rs1414785755 Functional Loss SNV dbSNP153 33..33 33 - - - 67785 RMVar_ID_67785 Human_SNP_ID_683836589 m1A Human chr20 - 51562675 51562675 51562675 GACGGCGTCCCCTCGGCTGCTGGTCGATACAAACAGATCCCCCTTTCCAAACACGCGCCAAGTCC GACGGCGTCCCCTCGGCTGCTGGTCGATACAATCAGATCCCCCTTTCCAAACACGCGCCAAGTCC T A NFATC2 Ensembl:ENSG00000101096 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:51562647..51562775 26863196 MeRIP-seq:(Medium) rs368892334 Functional Loss SNV dbSNP153 33..33 33 - - - 67786 RMVar_ID_67786 Human_SNP_ID_683836665 m1A Human chr20 - 51562931 51562931 51562931 GTTTTGGAGATGGACGGGATCCAGTGGTTTCCATGGCGCTGGATAAACAGGAGGAAACAGTGAGG GTTTTGGAGATGGACGGGATCCAGTGGTTTCCCTGGCGCTGGATAAACAGGAGGAAACAGTGAGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51562891..51563008 26863196 MeRIP-seq:(Medium) rs1241725678 Functional Loss SNV dbSNP153 33..33 33 - - - 67787 RMVar_ID_67787 Human_SNP_ID_683850551 m1A Human chr20 - 51618712 51618712 51618712 CTGCTGCCGATGTGCCCCCACCCAGAAGGCCCAGATCGTGCGCCTGCTTCAGGAGCGCACGGGCA CTGCTGCCGATGTGCCCCCACCCAGAAGGCCCGGATCGTGCGCCTGCTTCAGGAGCGCACGGGCA T C ATP9A Ensembl:ENSG00000054793 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:51618633..51618715 26863196 MeRIP-seq:(Medium) rs1013341656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19004440,Human_RBP_ID_26344074 Human_Splice_Rec_2094798,Human_Splice_Rec_2094799,Human_Splice_Rec_2094852,Human_Splice_Rec_2094853 RMVar_hsa_circ_1807,RMVar_hsa_circ_210880,RMVar_hsa_circ_86126,RMVar_hsa_circ_116262,RMVar_hsa_circ_121249,RMVar_hsa_circ_122087,RMVar_hsa_circ_376871,RMVar_hsa_circ_117651,RMVar_hsa_circ_119116,RMVar_hsa_circ_116339,RMVar_hsa_circ_106769,RMVar_hsa_circ_114733,RMVar_hsa_circ_100629,RMVar_hsa_circ_78219,RMVar_hsa_circ_83892,RMVar_hsa_circ_80050,RMVar_hsa_circ_210884,RMVar_hsa_circ_210885,RMVar_hsa_circ_210882,RMVar_hsa_circ_210883,RMVar_hsa_circ_210881,RMVar_hsa_circ_210872,RMVar_hsa_circ_210876,RMVar_hsa_circ_210878,RMVar_hsa_circ_210879,RMVar_hsa_circ_210877,RMVar_hsa_circ_210874,RMVar_hsa_circ_210875,RMVar_hsa_circ_210873,RMVar_hsa_circ_96472,RMVar_hsa_circ_100800,RMVar_hsa_circ_376319,RMVar_hsa_circ_122386,RMVar_hsa_circ_210896,RMVar_hsa_circ_210897,RMVar_hsa_circ_210898,RMVar_hsa_circ_210900,RMVar_hsa_circ_116670,RMVar_hsa_circ_58520,RMVar_hsa_circ_347270,RMVar_hsa_circ_104262,RMVar_hsa_circ_210901,RMVar_hsa_circ_210903,RMVar_hsa_circ_374510,RMVar_hsa_circ_270704,RMVar_hsa_circ_77279,RMVar_hsa_circ_210904,RMVar_hsa_circ_210906,RMVar_hsa_circ_210907,RMVar_hsa_circ_210905,RMVar_hsa_circ_275017,RMVar_hsa_circ_323600,RMVar_hsa_circ_376326,RMVar_hsa_circ_311630,RMVar_hsa_circ_24908,RMVar_hsa_circ_210908,RMVar_hsa_circ_210909,RMVar_hsa_circ_210910,RMVar_hsa_circ_105133,RMVar_hsa_circ_265851,RMVar_hsa_circ_266330,RMVar_hsa_circ_210911 67788 RMVar_ID_67788 Human_SNP_ID_683853449 m1A Human chr20 + 51628939 51628939 51628939 CCTTACCATGCAAGGGGCTGCCTCTGCAGAACATGCTTCCAAGGCCTGGTTTAACTTCCTGCATC CCTTACCATGCAAGGGGCTGCCTCTGCAGAACCTGCTTCCAAGGCCTGGTTTAACTTCCTGCATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:51628937..51629108 26863196 MeRIP-seq:(Medium) rs968643317 Functional Loss SNV dbSNP153 33..33 33 - - - 67789 RMVar_ID_67789 Human_SNP_ID_683881611 m1A Human chr20 - 51729907 51729907 51729907 CAGGCCCCGCACTGTCTGGCTGGGGCACCCCGAGAAGAGAGACCAGAGGTATCCTCGGAATGTCA CAGGCCCCGCACTGTCTGGCTGGGGCACCCCGGGAAGAGAGACCAGAGGTATCCTCGGAATGTCA T C ATP9A Ensembl:ENSG00000054793 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:51729826..51730022 26863196 MeRIP-seq:(Medium) rs1416683381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2094770,Human_Splice_Rec_2094771,Human_Splice_Rec_2094814,Human_Splice_Rec_2094815,Human_Splice_Rec_2094868,Human_Splice_Rec_2094869 Human_miRNA_ID_1078676,Human_miRNA_ID_3092150 RMVar_hsa_circ_121249,RMVar_hsa_circ_83892,RMVar_hsa_circ_210872,RMVar_hsa_circ_210873,RMVar_hsa_circ_96472,RMVar_hsa_circ_122386,RMVar_hsa_circ_210898,RMVar_hsa_circ_210901,RMVar_hsa_circ_113227,RMVar_hsa_circ_76249,RMVar_hsa_circ_210912,RMVar_hsa_circ_210913,RMVar_hsa_circ_346156,RMVar_hsa_circ_210920,RMVar_hsa_circ_369802,RMVar_hsa_circ_210934,RMVar_hsa_circ_352063,RMVar_hsa_circ_210947,RMVar_hsa_circ_365646,RMVar_hsa_circ_103357,RMVar_hsa_circ_210950,RMVar_hsa_circ_210955,RMVar_hsa_circ_270672,RMVar_hsa_circ_210959,RMVar_hsa_circ_210961,RMVar_hsa_circ_273737,RMVar_hsa_circ_210962,RMVar_hsa_circ_374904 67790 RMVar_ID_67790 Human_SNP_ID_683881616 m1A Human chr20 - 51729913 51729913 51729913 GGAGGCCAGGCCCCGCACTGTCTGGCTGGGGCACCCCGAGAAGAGAGACCAGAGGTATCCTCGGA GGAGGCCAGGCCCCGCACTGTCTGGCTGGGGCGCCCCGAGAAGAGAGACCAGAGGTATCCTCGGA T C ATP9A Ensembl:ENSG00000054793 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51729863..51730030 26863196 MeRIP-seq:(Medium) rs1454490034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659479 Human_Splice_Rec_2094770,Human_Splice_Rec_2094771,Human_Splice_Rec_2094814,Human_Splice_Rec_2094815,Human_Splice_Rec_2094868,Human_Splice_Rec_2094869 RMVar_hsa_circ_121249,RMVar_hsa_circ_83892,RMVar_hsa_circ_210872,RMVar_hsa_circ_210873,RMVar_hsa_circ_96472,RMVar_hsa_circ_122386,RMVar_hsa_circ_210898,RMVar_hsa_circ_210901,RMVar_hsa_circ_113227,RMVar_hsa_circ_76249,RMVar_hsa_circ_210912,RMVar_hsa_circ_210913,RMVar_hsa_circ_346156,RMVar_hsa_circ_210920,RMVar_hsa_circ_369802,RMVar_hsa_circ_210934,RMVar_hsa_circ_352063,RMVar_hsa_circ_210947,RMVar_hsa_circ_365646,RMVar_hsa_circ_103357,RMVar_hsa_circ_210950,RMVar_hsa_circ_210955,RMVar_hsa_circ_270672,RMVar_hsa_circ_210959,RMVar_hsa_circ_210961,RMVar_hsa_circ_273737,RMVar_hsa_circ_210962,RMVar_hsa_circ_374904 67791 RMVar_ID_67791 Human_SNP_ID_683881620 m1A Human chr20 + 51729925 51729925 51729925 TCTGGTCTCTCTTCTCGGGGTGCCCCAGCCAGACAGTGCGGGGCCTGGCCTCCCCTCCACCGCAG TCTGGTCTCTCTTCTCGGGGTGCCCCAGCCAGGCAGTGCGGGGCCTGGCCTCCCCTCCACCGCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51729874..51730033 26863196 MeRIP-seq:(Medium) rs762641868 Functional Loss SNV dbSNP153 33..33 33 - - - 67792 RMVar_ID_67792 Human_SNP_ID_683892927 m1A Human chr20 + 51769264 51769264 51769264 CTTTCATCCAAACACCCTTCAATAGTCTGAACACCCTCATTCTCACACCAGCCACTTTCTTGGGC CTTTCATCCAAACACCCTTCAATAGTCTGAACCCCCTCATTCTCACACCAGCCACTTTCTTGGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51769215..51769403 26863196 MeRIP-seq:(Medium) rs924979748 Functional Loss SNV dbSNP153 33..33 33 - - - 67793 RMVar_ID_67793 Human_SNP_ID_683901728 m1A Human chr20 + 51801901 51801901 51801901 CGGGGTTCTTTCTTTTGAGAGCGACGCGAGGGAGGGGGACCTAAGTTACAAGGGGGGGGGGTAAC CGGGGTTCTTTCTTTTGAGAGCGACGCGAGGGGGGGGGACCTAAGTTACAAGGGGGGGGGGTAAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:51801851..51802024 26863196 MeRIP-seq:(Medium) rs1219903187 Functional Loss SNV dbSNP153 33..33 33 - - - 67794 RMVar_ID_67794 Human_SNP_ID_683907138 m1A Human chr20 - 51821535 51821533 51821536 AGAGAGAAAGAGAGAAAGGAGAAAAGGAAAGAAGGAGAGGAAGGAAAGAAGGAAGGAAGGAAGGA AGAGAGAAAGAGAGAAAGGAGAAAAGGAAAG___GAGAGGAAGGAAAGAAGGAAGGAAGGAAGGA CCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51821488..51821576 26863196 MeRIP-seq:(Medium) rs1378794760 Functional Loss DEL dbSNP153 32..34 33 - - - 67795 RMVar_ID_67795 Human_SNP_ID_683909077 m1A Human chr20 - 51828714 51828714 51828714 TTATAATCTCTCCCATCTTTAAAACAAAAACAAAACCCTCCCTTGGCCACCATCCGTCTAGCAAC TTATAATCTCTCCCATCTTTAAAACAAAAACAGAACCCTCCCTTGGCCACCATCCGTCTAGCAAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:51828701..51828750 26863196 MeRIP-seq:(Medium) rs1296728551 Functional Loss SNV dbSNP153 33..33 33 - - - 67796 RMVar_ID_67796 Human_SNP_ID_683909144 m1A Human chr20 - 51829020 51829020 51829020 GGTGGGAGGACTCAGGGAAAAGCCAGGGAGCCAGGGGGCCAGAGCAGAAGTGGGAACAGGGCTGA GGTGGGAGGACTCAGGGAAAAGCCAGGGAGCCGGGGGGCCAGAGCAGAAGTGGGAACAGGGCTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51828971..51829259 26863196 MeRIP-seq:(Medium) rs1022472707 Functional Loss SNV dbSNP153 33..33 33 - - - 67797 RMVar_ID_67797 Human_SNP_ID_683910807 m1A Human chr20 + 51835242 51835242 51835242 CACCCTCACCAGCCCAGTTGCTCAAGCTGTCCATGATCCTTCTCATCATTGCCACTTTCACTCCA CACCCTCACCAGCCCAGTTGCTCAAGCTGTCCGTGATCCTTCTCATCATTGCCACTTTCACTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:51835191..51835275 26863196 MeRIP-seq:(Medium) rs1466008816 Functional Loss SNV dbSNP153 33..33 33 - - - 67798 RMVar_ID_67798 Human_SNP_ID_683911011 m1A Human chr20 - 51836046 51836046 51836046 GGTATTCCAAGCCCGGAGAACAGCAAGTGCACAGGCACTGAAGCTGGATCTGCTTGTTATATTGG GGTATTCCAAGCCCGGAGAACAGCAAGTGCACTGGCACTGAAGCTGGATCTGCTTGTTATATTGG T A LINC01429 Ensembl:ENSG00000227964 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51835995..51836079 26863196 MeRIP-seq:(Medium) rs1404329111 Functional Loss SNV dbSNP153 33..33 33 - - - 67799 RMVar_ID_67799 Human_SNP_ID_683911012 m1A Human chr20 - 51836046 51836046 51836046 GGTATTCCAAGCCCGGAGAACAGCAAGTGCACAGGCACTGAAGCTGGATCTGCTTGTTATATTGG GGTATTCCAAGCCCGGAGAACAGCAAGTGCACGGGCACTGAAGCTGGATCTGCTTGTTATATTGG T C LINC01429 Ensembl:ENSG00000227964 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51835995..51836079 26863196 MeRIP-seq:(Medium) rs1404329111 Functional Loss SNV dbSNP153 33..33 33 - - - 67800 RMVar_ID_67800 Human_SNP_ID_683918094 m1A Human chr20 - 51861545 51861542 51861546 ATAAATGTTGGAAGGAAGGAAAGAAAAGAAGGAAGAATGGACAGATAGGTGAATAAATGATAGAA ATAAATGTTGGAAGGAAGGAAAGAAAAGAAG____AATGGACAGATAGGTGAATAAATGATAGAA TCTTC T LINC01429 Ensembl:ENSG00000227964 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:51842737..51862938 26863196 MeRIP-seq:(Medium) rs1450985271 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_210964 67801 RMVar_ID_67801 Human_SNP_ID_683918095 m1A Human chr20 - 51861548 51861546 51861549 TGGATAAATGTTGGAAGGAAGGAAAGAAAAGAAGGAAGAATGGACAGATAGGTGAATAAATGATA TGGATAAATGTTGGAAGGAAGGAAAGAAAAG___GAAGAATGGACAGATAGGTGAATAAATGATA CCTT C LINC01429 Ensembl:ENSG00000227964 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:51842737..51862930;chr20:51861342..51861600 26863196 MeRIP-seq:(Medium) rs946608448 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_210964 67802 RMVar_ID_67802 Human_SNP_ID_683918454 m1A Human chr20 - 51862852 51862852 51862852 GAGAGGACCCTTGGACCATGGGGATGGGAGCAACGTGCCAGGCATGGCAGCGCAATAGAGGTGGG GAGAGGACCCTTGGACCATGGGGATGGGAGCAGCGTGCCAGGCATGGCAGCGCAATAGAGGTGGG T C LINC01429 Ensembl:ENSG00000227964 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:51862765..51862890 26863196 MeRIP-seq:(Medium) rs1473116422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2094895 RMVar_hsa_circ_210964 67803 RMVar_ID_67803 Human_SNP_ID_683976553 m1A Human chr20 - 52088575 52088575 52088575 GCTTCAGCCGGAAGGACAACCTGACCATGCACATGCGGTGCCACACCAGTGTGAAGCCACACAAG GCTTCAGCCGGAAGGACAACCTGACCATGCACTTGCGGTGCCACACCAGTGTGAAGCCACACAAG T A ZFP64 Ensembl:ENSG00000020256 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:52088526..52088575 32194978 MeRIP-seq:(Medium) rs1415188800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1599183,Human_RBP_ID_1931603,Human_RBP_ID_4652994,Human_RBP_ID_18775325 Human_Splice_Rec_2094912,Human_Splice_Rec_2094920,Human_Splice_Rec_2094936,Human_Splice_Rec_2094942,Human_Splice_Rec_2094950,Human_Splice_Rec_2094956 RMVar_hsa_circ_26834,RMVar_hsa_circ_85485,RMVar_hsa_circ_210966 67804 RMVar_ID_67804 Human_SNP_ID_683976554 m1A Human chr20 - 52088575 52088575 52088575 GCTTCAGCCGGAAGGACAACCTGACCATGCACATGCGGTGCCACACCAGTGTGAAGCCACACAAG GCTTCAGCCGGAAGGACAACCTGACCATGCACGTGCGGTGCCACACCAGTGTGAAGCCACACAAG T C ZFP64 Ensembl:ENSG00000020256 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:52088526..52088575 32194978 MeRIP-seq:(Medium) rs1415188800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1599183,Human_RBP_ID_1931603,Human_RBP_ID_4652994,Human_RBP_ID_18775325 Human_Splice_Rec_2094912,Human_Splice_Rec_2094920,Human_Splice_Rec_2094936,Human_Splice_Rec_2094942,Human_Splice_Rec_2094950,Human_Splice_Rec_2094956 RMVar_hsa_circ_26834,RMVar_hsa_circ_85485,RMVar_hsa_circ_210966 67805 RMVar_ID_67805 Human_SNP_ID_684197121 m1A Human chr20 + 52972467 52972463 52972467 GTTTGTGTGTGTGTGCATATGTGGGGGGTGTGAGTGTGTGTGTGCGAGGAAGCGGGGGTGCGTGC GTTTGTGTGTGTGTGCATATGTGGGGGGT____GTGTGTGTGTGCGAGGAAGCGGGGGTGCGTGC TGTGA T TSHZ2 Ensembl:ENSG00000182463 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:52972337..52972580 26863196 MeRIP-seq:(Medium) rs1021878888 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23910794 67806 RMVar_ID_67806 Human_SNP_ID_684197425 m1A Human chr20 - 52973251 52973251 52973251 GCTCCAGTCCCACTTCTGGCGCCCCAGCCCCGAGCCGCGCGCTGGGGCCCGCTGTCTCTCTGGCC GCTCCAGTCCCACTTCTGGCGCCCCAGCCCCGCGCCGCGCGCTGGGGCCCGCTGTCTCTCTGGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:52973201..52973434 26863196 MeRIP-seq:(Medium) rs200347939 Functional Loss SNV dbSNP153 33..33 33 - - - 67807 RMVar_ID_67807 Human_SNP_ID_684197438 m1A Human chr20 + 52973270 52973270 52973270 CCCAGCGCGCGGCTCGGGGCTGGGGCGCCAGAAGTGGGACTGGAGCGAAGTAGAGGATGCCGAGG CCCAGCGCGCGGCTCGGGGCTGGGGCGCCAGATGTGGGACTGGAGCGAAGTAGAGGATGCCGAGG A T TSHZ2 Ensembl:ENSG00000182463 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:52973001..52973359 26863196 MeRIP-seq:(Medium) rs1361603448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2095637 67808 RMVar_ID_67808 Human_SNP_ID_684201898 m1A Human chr20 - 52990497 52990497 52990497 TGAGGACAAGTGTGATTTCTTTTCTGTTGTTCATGCTTTTCTTTTTACTTCTCCCTGTTCCCCAC TGAGGACAAGTGTGATTTCTTTTCTGTTGTTCCTGCTTTTCTTTTTACTTCTCCCTGTTCCCCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:52990489..52990585 26863196 MeRIP-seq:(Medium) rs1332516412 Functional Loss SNV dbSNP153 33..33 33 - - - 67809 RMVar_ID_67809 Human_SNP_ID_684206476 m1A Human chr20 - 53007159 53007159 53007159 CCTGGTCAACTCCTGCTAAGCCTTCAAGTATCAAGTTCAATGCCACCTCCTCAGGGAAGCCTTTC CCTGGTCAACTCCTGCTAAGCCTTCAAGTATCGAGTTCAATGCCACCTCCTCAGGGAAGCCTTTC T C HSALNG0130913 RNACentral:URS0000E941EC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53007150..53007301 26863196 MeRIP-seq:(Medium) rs1346008320 Functional Loss SNV dbSNP153 33..33 33 - - - 67810 RMVar_ID_67810 Human_SNP_ID_684208495 m1A Human chr20 - 53014846 53014846 53014846 ACACAAACGAACAGACGACTCATTCTGTACGAAGCGTTGTACTGGGGCTTCAGGGAGGTGGAGGG ACACAAACGAACAGACGACTCATTCTGTACGAGGCGTTGTACTGGGGCTTCAGGGAGGTGGAGGG T C HSALNG0130913 RNACentral:URS0000E941EC lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:53014837..53015122 26863196 MeRIP-seq:(Medium) rs1432781502 Functional Loss SNV dbSNP153 33..33 33 - - - 67811 RMVar_ID_67811 Human_SNP_ID_684233975 m1A Human chr20 + 53115619 53115619 53115619 GAGAACAGACTAATACAGGTGGCATGACAAAAATAAGTAAATAAATGACACAGAGCAAAGGAATT GAGAACAGACTAATACAGGTGGCATGACAAAACTAAGTAAATAAATGACACAGAGCAAAGGAATT A C TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53115613..53115836 26863196 MeRIP-seq:(Medium) rs6022285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2689666 GWAS_ID_8100,GWAS_ID_8101,GWAS_ID_8102,GWAS_ID_8103,GWAS_ID_8104,GWAS_ID_8105,GWAS_ID_8106,GWAS_ID_8107 67812 RMVar_ID_67812 Human_SNP_ID_684233988 m1A Human chr20 - 53115651 53115651 53115651 CCTCCCCACCTCTGCACCTCACTACCATTCTCAATTCCTTTGCTCTGTGTCATTTATTTACTTAT CCTCCCCACCTCTGCACCTCACTACCATTCTCTATTCCTTTGCTCTGTGTCATTTATTTACTTAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53115643..53115897 26863196 MeRIP-seq:(Medium) rs776813027 Functional Loss SNV dbSNP153 33..33 33 - - - 67813 RMVar_ID_67813 Human_SNP_ID_684263217 m1A Human chr20 + 53229888 53229888 53229888 ATGGAAAGAAAAGAGGGAGGAAGAAAGGAAGGAAAAGAGAGAGGGAGGGGAAAAAAAGAGAAAGA ATGGAAAGAAAAGAGGGAGGAAGAAAGGAAGGGAAAGAGAGAGGGAGGGGAAAAAAAGAGAAAGA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53229886..53230008 26863196 MeRIP-seq:(Medium) rs552826468 Functional Loss SNV dbSNP153 33..33 33 - - - 67814 RMVar_ID_67814 Human_SNP_ID_684269217 m1A Human chr20 + 53253581 53253581 53253581 GAGGAGGAGGAGGACAGCGGTTCAGTAGCTCAACTGCAGGGTGGCAATGACACAGGGACGGACGA GAGGAGGAGGAGGACAGCGGTTCAGTAGCTCAGCTGCAGGGTGGCAATGACACAGGGACGGACGA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53253463..53253762 26863196 MeRIP-seq:(Medium) rs756735462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8536253 Human_Splice_Rec_2095638,Human_Splice_Rec_2095642,Human_Splice_Rec_2095646 RMVar_hsa_circ_210970,RMVar_hsa_circ_274117,RMVar_hsa_circ_210971 67815 RMVar_ID_67815 Human_SNP_ID_684269218 m1A Human chr20 + 53253581 53253581 53253581 GAGGAGGAGGAGGACAGCGGTTCAGTAGCTCAACTGCAGGGTGGCAATGACACAGGGACGGACGA GAGGAGGAGGAGGACAGCGGTTCAGTAGCTCATCTGCAGGGTGGCAATGACACAGGGACGGACGA A T TSHZ2 Ensembl:ENSG00000182463 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53253463..53253762 26863196 MeRIP-seq:(Medium) rs756735462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8536253 Human_Splice_Rec_2095638,Human_Splice_Rec_2095642,Human_Splice_Rec_2095646 RMVar_hsa_circ_210970,RMVar_hsa_circ_274117,RMVar_hsa_circ_210971 67816 RMVar_ID_67816 Human_SNP_ID_684269433 m1A Human chr20 + 53254026 53254026 53254026 AGAACTTGCCTTCTCGGTCCGTCTCGAAACCCAGCCTGTTCAGCTCGGTGCAGTTGTACCGACAG AGAACTTGCCTTCTCGGTCCGTCTCGAAACCCGGCCTGTTCAGCTCGGTGCAGTTGTACCGACAG A G TSHZ2 Ensembl:ENSG00000182463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:53253976..53254050 26863196 MeRIP-seq:(Medium) rs370108973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210970,RMVar_hsa_circ_274117,RMVar_hsa_circ_210971 67817 RMVar_ID_67817 Human_SNP_ID_684272433 m1A Human chr20 + 53265265 53265265 53265265 GTCCCAGTGAGAACATTCAAATGCATTGAGCCAGACAGGGAAGGCACACTTAGGGGCTTGGAAGA GTCCCAGTGAGAACATTCAAATGCATTGAGCCGGACAGGGAAGGCACACTTAGGGGCTTGGAAGA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53265215..53265463 26863196 MeRIP-seq:(Medium) rs1416865527 Functional Loss SNV dbSNP153 33..33 33 - - - 67818 RMVar_ID_67818 Human_SNP_ID_684273305 m1A Human chr20 + 53268835 53268835 53268835 ATGCTCAGCAAATCTGAGCTATTATTTTTATCACGACTGTCAGAGGTCAGATCAGGCTTCGGGGT ATGCTCAGCAAATCTGAGCTATTATTTTTATCGCGACTGTCAGAGGTCAGATCAGGCTTCGGGGT A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53268689..53268980 26863196 MeRIP-seq:(Medium) rs1352201616 Functional Loss SNV dbSNP153 33..33 33 - - - 67819 RMVar_ID_67819 Human_SNP_ID_684284952 m1A Human chr20 - 53315842 53315842 53315842 CTGTGTATTTCTCATACCAACGTAGGCCCCTAAAATCTAGCTTCTACCCTTTCTGCTTTTCCTTC CTGTGTATTTCTCATACCAACGTAGGCCCCTACAATCTAGCTTCTACCCTTTCTGCTTTTCCTTC T G AL109930.1 Ensembl:ENSG00000271774 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53315827..53316021 26863196 MeRIP-seq:(Medium) rs200655 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8108,GWAS_ID_8109,GWAS_ID_8110,GWAS_ID_8111,GWAS_ID_8112,GWAS_ID_8113,GWAS_ID_8114,GWAS_ID_8115,GWAS_ID_8116 67820 RMVar_ID_67820 Human_SNP_ID_684289523 m1A Human chr20 + 53334231 53334228 53334232 ATGTATCAGATAGTAAGCCCTGAGAAAAATAAAGAGAGAAAAAAACAACAGCTCGTGGGAGGGGG ATGTATCAGATAGTAAGCCCTGAGAAAAAT____AGAGAAAAAAACAACAGCTCGTGGGAGGGGG TAAAG T TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53334181..53334328 26863196 MeRIP-seq:(Medium) rs1471098347 Functional Loss DEL dbSNP153 31..34 33 - - - 67821 RMVar_ID_67821 Human_SNP_ID_684289525 m1A Human chr20 + 53334231 53334230 53334232 ATGTATCAGATAGTAAGCCCTGAGAAAAATAAAGAGAGAAAAAAACAACAGCTCGTGGGAGGGGG ATGTATCAGATAGTAAGCCCTGAGAAAAATAA__AGAGAAAAAAACAACAGCTCGTGGGAGGGGG AAG A TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53334181..53334328 26863196 MeRIP-seq:(Medium) rs1261540935 Functional Loss DEL dbSNP153 33..34 33 - - - 67822 RMVar_ID_67822 Human_SNP_ID_684289526 m1A Human chr20 + 53334231 53334231 53334231 ATGTATCAGATAGTAAGCCCTGAGAAAAATAAAGAGAGAAAAAAACAACAGCTCGTGGGAGGGGG ATGTATCAGATAGTAAGCCCTGAGAAAAATAAGGAGAGAAAAAAACAACAGCTCGTGGGAGGGGG A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53334181..53334328 26863196 MeRIP-seq:(Medium) rs1476453607 Functional Loss SNV dbSNP153 33..33 33 - - - 67823 RMVar_ID_67823 Human_SNP_ID_684323340 m1A Human chr20 + 53469708 53469702 53469708 GGAAGGAAGGACGGACCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAG GGAAGGAAGGACGGACCCAAGAAAGAT______AGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAG TAGAGAA T TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:53469573..53469931 26863196 MeRIP-seq:(Medium) rs1465162711 Functional Loss DEL dbSNP153 28..33 33 - - - 67824 RMVar_ID_67824 Human_SNP_ID_684323341 m1A Human chr20 + 53469709 53469702 53469710 GAAGGAAGGACGGACCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG GAAGGAAGGACGGACCCAAGAAAGAT________AGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG TAGAGAAAG T TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53469538..53469894 26863196 MeRIP-seq:(Medium) rs1568932041 Functional Loss DEL dbSNP153 27..34 33 - - - 67825 RMVar_ID_67825 Human_SNP_ID_684323347 m1A Human chr20 + 53469708 53469704 53469708 GGAAGGAAGGACGGACCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAG GGAAGGAAGGACGGACCCAAGAAAGATAG____AGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAG GAGAA G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:53469573..53469931 26863196 MeRIP-seq:(Medium) rs1481771867 Functional Loss DEL dbSNP153 30..33 33 - - - 67826 RMVar_ID_67826 Human_SNP_ID_684323349 m1A Human chr20 + 53469709 53469708 53469710 GAAGGAAGGACGGACCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG GAAGGAAGGACGGACCCAAGAAAGATAGAGAA__AGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG AAG A TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53469538..53469894 26863196 MeRIP-seq:(Medium) rs1247084171 Functional Loss DEL dbSNP153 33..34 33 - - - 67827 RMVar_ID_67827 Human_SNP_ID_684323351 m1A Human chr20 + 53469709 53469709 53469709 GAAGGAAGGACGGACCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG GAAGGAAGGACGGACCCAAGAAAGATAGAGAACGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAGG A C TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53469538..53469894 26863196 MeRIP-seq:(Medium) rs1177970085 Functional Loss SNV dbSNP153 33..33 33 - - - 67828 RMVar_ID_67828 Human_SNP_ID_684323366 m1A Human chr20 + 53469723 53469723 53469723 CCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAAGGGAGGGAGGAAGGAAGGAAGGACCCAAGAAA CCCAAGAAAGATAGAGAAAGAGAGAGGGAGGAGGGGAGGGAGGAAGGAAGGAAGGACCCAAGAAA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53469672..53469883 26863196 MeRIP-seq:(Medium) rs1243573923 Functional Loss SNV dbSNP153 33..33 33 - - - 67829 RMVar_ID_67829 Human_SNP_ID_684355446 m1A Human chr20 + 53583158 53583158 53583158 AGAAGTCAATCCCAGCAACCTGGAGACAAGGGATTTCCAAACCCTAGAGGAAAAAAAACAGAAAC AGAAGTCAATCCCAGCAACCTGGAGACAAGGGGTTTCCAAACCCTAGAGGAAAAAAAACAGAAAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:53583123..53583224 26863410 MeRIP-seq:(Medium) rs1354264884 Functional Loss SNV dbSNP153 33..33 33 - - - 67830 RMVar_ID_67830 Human_SNP_ID_684357893 m1A Human chr20 + 53592625 53592625 53592625 GCCCTGAACATCTTCTCAAACTCCCGGGACCCAGGTTCCGGCGCGCGCCCCGCGTGCCGGGTCTT GCCCTGAACATCTTCTCAAACTCCCGGGACCCGGGTTCCGGCGCGCGCCCCGCGTGCCGGGTCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:53592622..53592713 26863196 MeRIP-seq:(Medium) rs1029989518 Functional Loss SNV dbSNP153 33..33 33 - - - 67831 RMVar_ID_67831 Human_SNP_ID_684358324 m1A Human chr20 - 53593614 53593614 53593614 AGGATGACCTCAGTTCCCCGTCTCAGCTTTCTATCCGCTCCTCTAGGGCGCCCCCTCCCCAGCCG AGGATGACCTCAGTTCCCCGTCTCAGCTTTCTGTCCGCTCCTCTAGGGCGCCCCCTCCCCAGCCG T C ZNF217 Ensembl:ENSG00000171940 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53593565..53593649 26863196 MeRIP-seq:(Medium) rs940021777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18950775 67832 RMVar_ID_67832 Human_SNP_ID_684358424 m1A Human chr20 - 53593769 53593769 53593769 CCGGCCGCCGCCGCGCGAGGAAATGGCCGAGGAGCCGGAGCCGCAGGTAAAGGGGGCGCGCCCCC CCGGCCGCCGCCGCGCGAGGAAATGGCCGAGGGGCCGGAGCCGCAGGTAAAGGGGGCGCGCCCCC T C ZNF217 Ensembl:ENSG00000171940 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:53593538..53593783 26863196 MeRIP-seq:(Medium) rs28680541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659917,Human_RBP_ID_5148497,Human_RBP_ID_5529469,Human_RBP_ID_18422929 Human_Splice_Rec_2095685 67833 RMVar_ID_67833 Human_SNP_ID_684358633 m1A Human chr20 - 53594141 53594141 53594141 TAGGGGGCGCCCGCGCCTTTGCCCCCGTGCGCACCCCCGCCCCGCTCACCTTAGCCCCGCGCCCG TAGGGGGCGCCCGCGCCTTTGCCCCCGTGCGCCCCCCCGCCCCGCTCACCTTAGCCCCGCGCCCG T G ZNF217 Ensembl:ENSG00000171940 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:53594128..53594246 26863196 MeRIP-seq:(Medium) rs1014654592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17974283 67834 RMVar_ID_67834 Human_SNP_ID_684517236 m1A Human chr20 + 54214356 54214356 54214356 TTACAAAAACTTAAACACTTCTTTCAGGCTGCAGAAGATGTCAATGTTACTTTCGAAGATCAACA TTACAAAAACTTAAACACTTCTTTCAGGCTGCGGAAGATGTCAATGTTACTTTCGAAGATCAACA A G PFDN4 Ensembl:ENSG00000101132 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:54214351..54214475 26863196 MeRIP-seq:(Medium) rs769758966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2690428,Human_RBP_ID_7013879,Human_RBP_ID_9389550,Human_RBP_ID_24546696,Human_RBP_ID_26343776 Human_Splice_Rec_2095868,Human_Splice_Rec_2095874,Human_Splice_Rec_2095884,Human_Splice_Rec_2095892,Human_Splice_Rec_2095898 RMVar_hsa_circ_17664,RMVar_hsa_circ_331217 67835 RMVar_ID_67835 Human_SNP_ID_684517241 m1A Human chr20 + 54214372 54214369 54214373 ACTTCTTTCAGGCTGCAGAAGATGTCAATGTTACTTTCGAAGATCAACAAAAGATAAACAAATTT ACTTCTTTCAGGCTGCAGAAGATGTCAATG____TTTCGAAGATCAACAAAAGATAAACAAATTT GTTAC G PFDN4 Ensembl:ENSG00000101132 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:54214338..54214443 26863410 MeRIP-seq:(Medium) rs1568676405 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_63432,Human_RBP_ID_2690429,Human_RBP_ID_9389551,Human_RBP_ID_24546696,Human_RBP_ID_26343776,Human_RBP_ID_26671781,Human_RBP_ID_27023025,Human_RBP_ID_27819928 Human_Splice_Rec_2095868,Human_Splice_Rec_2095869,Human_Splice_Rec_2095874,Human_Splice_Rec_2095875,Human_Splice_Rec_2095884,Human_Splice_Rec_2095885,Human_Splice_Rec_2095892,Human_Splice_Rec_2095893,Human_Splice_Rec_2095898 RMVar_hsa_circ_17664,RMVar_hsa_circ_331217 67836 RMVar_ID_67836 Human_SNP_ID_684518397 m1A Human chr20 - 54219252 54219252 54219252 GGCAAGTTTCCATTAAATAAATGAAAATTTTTAAAAAAGAAAGTTTTGCTTTCCATGTCATTTGA GGCAAGTTTCCATTAAATAAATGAAAATTTTTTAAAAAGAAAGTTTTGCTTTCCATGTCATTTGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:54219187..54219336 32194978 MeRIP-seq:(Medium) rs1194589158 Functional Loss SNV dbSNP153 33..33 33 - - - 67837 RMVar_ID_67837 Human_SNP_ID_685077101 m1A Human chr20 - 56359099 56359099 56359099 GAGCAGGGCCAGGGCCAGGGGCGGCGGGGCGCAGGGGGCGGTGGCGCCCAGGAGCCAGGTGGCGC GAGCAGGGCCAGGGCCAGGGGCGGCGGGGCGCGGGGGGCGGTGGCGCCCAGGAGCCAGGTGGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr20:56359048..56359212;chr20:56358976..56359163 26863196,26863410 MeRIP-seq:(Medium) rs1326534722 Functional Loss SNV dbSNP153 33..33 33 - - - 67838 RMVar_ID_67838 Human_SNP_ID_685079979 m1A Human chr20 + 56370550 56370550 56370550 GTTTGCCTCAAAAGGAGGCTTCCCAACTAAAAATTCATAGCAAAGAACTCCAAGGCTCCAGAGAT GTTTGCCTCAAAAGGAGGCTTCCCAACTAAAACTTCATAGCAAAGAACTCCAAGGCTCCAGAGAT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:56370476..56370675 32194978 MeRIP-seq:(Medium) rs762567231 Functional Loss SNV dbSNP153 33..33 33 - - - 67839 RMVar_ID_67839 Human_SNP_ID_685082965 m1A Human chr20 + 56382978 56382978 56382978 TTGGTGAACATTCTTTTGAACATGAACCTGAAAACTCACCGAAGGTGGGACTGTATTTCTACTTC TTGGTGAACATTCTTTTGAACATGAACCTGAAGACTCACCGAAGGTGGGACTGTATTTCTACTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:56382976..56383200 32194978 MeRIP-seq:(Medium) rs1231885823 Functional Loss SNV dbSNP153 33..33 33 - - - 67840 RMVar_ID_67840 Human_SNP_ID_685083766 m1A Human chr20 - 56386308 56386308 56386308 TGCAGGCAACCAGTGTACCTCATCCTGTCTCCAGGCCACTGAATAACACCCAAAAGAGCAAGCAG TGCAGGCAACCAGTGTACCTCATCCTGTCTCCCGGCCACTGAATAACACCCAAAAGAGCAAGCAG T G AURKA Ensembl:ENSG00000087586 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56386228..56386397 26863196 MeRIP-seq:(Medium) rs747330076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5445781,Human_RBP_ID_7014445,Human_RBP_ID_8856162,Human_RBP_ID_9118331,Human_RBP_ID_9389558,Human_RBP_ID_22453577,Human_RBP_ID_27487346 Human_Splice_Rec_2096095,Human_Splice_Rec_2096113,Human_Splice_Rec_2096129,Human_Splice_Rec_2096147,Human_Splice_Rec_2096165,Human_Splice_Rec_2096181,Human_Splice_Rec_2096197,Human_Splice_Rec_2096213,Human_Splice_Rec_2096229,Human_Splice_Rec_2096245,Human_Splice_Rec_2096255 RMVar_hsa_circ_6928,RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_211025,RMVar_hsa_circ_4614,RMVar_hsa_circ_270962,RMVar_hsa_circ_294140,RMVar_hsa_circ_335191,RMVar_hsa_circ_211026,RMVar_hsa_circ_64209,RMVar_hsa_circ_307728,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_306324,RMVar_hsa_circ_211027 67841 RMVar_ID_67841 Human_SNP_ID_685083843 m1A Human chr20 + 56386525 56386525 56386525 GTCACGAGAACACGTTTTGGACCTCCAACTGGAGCTGTAGCCTAGAATGGAAGAGAAAATAAACT GTCACGAGAACACGTTTTGGACCTCCAACTGGGGCTGTAGCCTAGAATGGAAGAGAAAATAAACT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr20:56386385..56388315;chr20:56386251..56386550 26863410,32194978 MeRIP-seq:(Medium) rs200982776 Functional Loss SNV dbSNP153 33..33 33 - - - 67842 RMVar_ID_67842 Human_SNP_ID_685084275 m1A Human chr20 - 56388197 56388197 56388197 ATTAAAGGTTCTTCTTTTTCTTTTCAGGCATCATGGACCGATCTAAAGAAAACTGCATTTCAGGA ATTAAAGGTTCTTCTTTTTCTTTTCAGGCATCGTGGACCGATCTAAAGAAAACTGCATTTCAGGA T C AURKA Ensembl:ENSG00000087586 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:56388156..56388365 26863196 MeRIP-seq:(Medium) rs1237613782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1068355,Human_RBP_ID_1599405,Human_RBP_ID_14146520,Human_RBP_ID_24380377 Human_Splice_Rec_2096092,Human_Splice_Rec_2096093,Human_Splice_Rec_2096110,Human_Splice_Rec_2096111,Human_Splice_Rec_2096126,Human_Splice_Rec_2096127,Human_Splice_Rec_2096144,Human_Splice_Rec_2096145,Human_Splice_Rec_2096162,Human_Splice_Rec_2096163,Human_Splice_Rec_2096178,Human_Splice_Rec_2096179,Human_Splice_Rec_2096194,Human_Splice_Rec_2096195,Human_Splice_Rec_2096210,Human_Splice_Rec_2096211,Human_Splice_Rec_2096226,Human_Splice_Rec_2096227,Human_Splice_Rec_2096242,Human_Splice_Rec_2096243,Human_Splice_Rec_2096252,Human_Splice_Rec_2096253,Human_Splice_Rec_2096264,Human_Splice_Rec_2096265,Human_Splice_Rec_2096272,Human_Splice_Rec_2096273 RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_4614,RMVar_hsa_circ_294140,RMVar_hsa_circ_335191,RMVar_hsa_circ_211026,RMVar_hsa_circ_64209,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_306324,RMVar_hsa_circ_211027 67843 RMVar_ID_67843 Human_SNP_ID_685084590 m1A Human chr20 - 56389453 56389453 56389453 AGTCATTCTAGGCCTGAGCTCAGGGCACACCCATGAACAGGGAGGTGAGAAGTGGAGAAGGGAAG AGTCATTCTAGGCCTGAGCTCAGGGCACACCCGTGAACAGGGAGGTGAGAAGTGGAGAAGGGAAG T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:56389451..56389677 26863196 MeRIP-seq:(Medium) rs1446185857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14146548 RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 67844 RMVar_ID_67844 Human_SNP_ID_685084703 m1A Human chr20 - 56389834 56389834 56389834 GGCAGAGCCTACAGAATATGCTGGTGGATTAAATGAAGGGTTTGCGAGAGAGAACCTCGTAAAGG GGCAGAGCCTACAGAATATGCTGGTGGATTAAGTGAAGGGTTTGCGAGAGAGAACCTCGTAAAGG T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:56389830..56389984 26863196 MeRIP-seq:(Medium) rs1414119603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27703290 RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 67845 RMVar_ID_67845 Human_SNP_ID_685085172 m1A Human chr20 + 56391685 56391685 56391685 CATTCATCAATTCACCCACTCATCCAGCCAGGACAAGGGCCTTCTTAGGCTATTCTATCTAAAGC CATTCATCAATTCACCCACTCATCCAGCCAGGGCAAGGGCCTTCTTAGGCTATTCTATCTAAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:56391683..56391849 26863196 MeRIP-seq:(Medium) rs536852203 Functional Loss SNV dbSNP153 33..33 33 - - - 67846 RMVar_ID_67846 Human_SNP_ID_685085270 m1A Human chr20 + 56392040 56392040 56392040 AGGCGCTGGGCGGGCACAAGGCAGCGCCAAGGACACTCAGGGACGGAGGAACCGACAGGGGACTT AGGCGCTGGGCGGGCACAAGGCAGCGCCAAGGTCACTCAGGGACGGAGGAACCGACAGGGGACTT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:56392038..56392210 26863410 MeRIP-seq:(Medium) rs1034907497 Functional Loss SNV dbSNP153 33..33 33 - - - 67847 RMVar_ID_67847 Human_SNP_ID_685085468 m1A Human chr20 + 56392556 56392556 56392556 CCTTTGAACGTGCCAGTAAGTAAGATGGCGAGAAAAGCAAGAGAGAGTGGGACCGATCGATAGCG CCTTTGAACGTGCCAGTAAGTAAGATGGCGAGGAAAGCAAGAGAGAGTGGGACCGATCGATAGCG A G CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56392420..56395526 26863196 MeRIP-seq:(Medium) rs2104015 Functional Loss SNV dbSNP153 33..33 33 - - - 67848 RMVar_ID_67848 Human_SNP_ID_685104427 m1A Human chr20 - 56468694 56468694 56468694 TTGGGGATTGTTCCCCCGTCGCAACCCATCGCAGGACGGGAGTCAGAGCCAGCAGCAAACCCCCA TTGGGGATTGTTCCCCCGTCGCAACCCATCGCGGGACGGGAGTCAGAGCCAGCAGCAAACCCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56468626..56468819 26863196 MeRIP-seq:(Medium) rs572142372 Functional Loss SNV dbSNP153 33..33 33 - - - 67849 RMVar_ID_67849 Human_SNP_ID_685104439 m1A Human chr20 + 56468726 56468726 56468726 TGCGATGGGTTGCGACGGGGGAACAATCCCCAAGAGGCATGAACTGGTGAAGGGGCCGAAGAAGG TGCGATGGGTTGCGACGGGGGAACAATCCCCAGGAGGCATGAACTGGTGAAGGGGCCGAAGAAGG A G RTF2 Ensembl:ENSG00000022277 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr20:56468651..56470616;chr20:56468676..56468775 32194978 MeRIP-seq:(Medium) rs1376731729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63360,Human_RBP_ID_566949,Human_RBP_ID_1599466,Human_RBP_ID_4659487,Human_RBP_ID_5503578,Human_RBP_ID_5529184,Human_RBP_ID_8536520,Human_RBP_ID_9118347,Human_RBP_ID_19006037,Human_RBP_ID_22080804,Human_RBP_ID_22453579,Human_RBP_ID_23912165,Human_RBP_ID_24546702,Human_RBP_ID_26343139,Human_RBP_ID_27819935 Human_Splice_Rec_2096357,Human_Splice_Rec_2096375,Human_Splice_Rec_2096391,Human_Splice_Rec_2096405,Human_Splice_Rec_2096413,Human_Splice_Rec_2096429,Human_Splice_Rec_2096437 67850 RMVar_ID_67850 Human_SNP_ID_685105376 m1A Human chr20 - 56472343 56472343 56472343 CCTTCACTGTGTAGACTGCACCACTCTTTCCCATTCTTCAAATGCCAAATCTGAATAATTTAACA CCTTCACTGTGTAGACTGCACCACTCTTTCCCCTTCTTCAAATGCCAAATCTGAATAATTTAACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:56472339..56473400 26863196 MeRIP-seq:(Medium) rs1356167160 Functional Loss SNV dbSNP153 33..33 33 - - - 67851 RMVar_ID_67851 Human_SNP_ID_685105621 m1A Human chr20 - 56473234 56473234 56473234 CTCTGAAAGACACATGGTTCACAATTCTACATATAAAAGTATATTCAGTAATACCGCACTGTAAT CTCTGAAAGACACATGGTTCACAATTCTACATCTAAAAGTATATTCAGTAATACCGCACTGTAAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:56473232..56473350 26863196 MeRIP-seq:(Medium) rs1183598112 Functional Loss SNV dbSNP153 33..33 33 - - - 67852 RMVar_ID_67852 Human_SNP_ID_685115921 m1A Human chr20 + 56513376 56513376 56513376 CATCATGCTCAATGGCACCAAGGAGGATGTGGACGTGCTGAAGACAAGGATGGAGGAGAGAAGGC CATCATGCTCAATGGCACCAAGGAGGATGTGGGCGTGCTGAAGACAAGGATGGAGGAGAGAAGGC A G RTF2 Ensembl:ENSG00000022277 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:56513326..56513450 32194978 MeRIP-seq:(Medium) rs1411779695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_566953,Human_RBP_ID_7014789,Human_RBP_ID_9389563,Human_RBP_ID_18193788,Human_RBP_ID_23005222,Human_RBP_ID_23912222,Human_RBP_ID_26343143,Human_RBP_ID_27820440 Human_Splice_Rec_2096368,Human_Splice_Rec_2096369,Human_Splice_Rec_2096384,Human_Splice_Rec_2096385,Human_Splice_Rec_2096400,Human_Splice_Rec_2096401,Human_Splice_Rec_2096424,Human_Splice_Rec_2096425,Human_Splice_Rec_2096449 Human_miRNA_ID_2490896 RMVar_hsa_circ_13844,RMVar_hsa_circ_105918,RMVar_hsa_circ_82374,RMVar_hsa_circ_377521,RMVar_hsa_circ_211032,RMVar_hsa_circ_94824,RMVar_hsa_circ_211034,RMVar_hsa_circ_211036,RMVar_hsa_circ_60669,RMVar_hsa_circ_117488,RMVar_hsa_circ_211037 67853 RMVar_ID_67853 Human_SNP_ID_685115939 m1A Human chr20 - 56513409 56513409 56513409 AGACTCCCATTACCTTTTCCAGCTTCGCTCTCAGCCTTCTCTCCTCCATCCTTGTCTTCAGCACG AGACTCCCATTACCTTTTCCAGCTTCGCTCTCGGCCTTCTCTCCTCCATCCTTGTCTTCAGCACG T C GCNT7 Ensembl:ENSG00000124091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56513276..56513475 26863196 MeRIP-seq:(Medium) rs774291056 Functional Loss SNV dbSNP153 33..33 33 - - - 67854 RMVar_ID_67854 Human_SNP_ID_685115946 m1A Human chr20 + 56513426 56513426 56513426 TGGAGGAGAGAAGGCTGAGAGCGAAGCTGGAAAAGGTAATGGGAGTCTTCAGGTTCCGCCCAGCC TGGAGGAGAGAAGGCTGAGAGCGAAGCTGGAATAGGTAATGGGAGTCTTCAGGTTCCGCCCAGCC A T RTF2 Ensembl:ENSG00000022277 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:56513401..56513450 26863196 MeRIP-seq:(Medium) rs1483609835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18193788,Human_RBP_ID_23005222,Human_RBP_ID_26343143,Human_RBP_ID_27820440 Human_Splice_Rec_2096369,Human_Splice_Rec_2096385,Human_Splice_Rec_2096401,Human_Splice_Rec_2096425,Human_Splice_Rec_2096449 RMVar_hsa_circ_13844,RMVar_hsa_circ_105918,RMVar_hsa_circ_82374,RMVar_hsa_circ_377521,RMVar_hsa_circ_211032,RMVar_hsa_circ_94824,RMVar_hsa_circ_211034,RMVar_hsa_circ_211036,RMVar_hsa_circ_60669,RMVar_hsa_circ_117488,RMVar_hsa_circ_211037 67855 RMVar_ID_67855 Human_SNP_ID_685186726 m1A Human chr20 + 56781425 56781425 56781425 ACAACAGGGGACATTTGGCAGTGTCTGGAGACATTTGTGGTTGTTGCGTCTGGAGAGAGGGGACG ACAACAGGGGACATTTGGCAGTGTCTGGAGACGTTTGTGGTTGTTGCGTCTGGAGAGAGGGGACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56781375..56781512 26863196 MeRIP-seq:(Medium) rs924770634 Functional Loss SNV dbSNP153 33..33 33 - - - 67856 RMVar_ID_67856 Human_SNP_ID_685187087 m1A Human chr20 + 56782316 56782316 56782316 AGGAAGGAAGAAAGGAAGGAAAGAAAGAAGGAAAGAACAAAAGGGAGAAAGGGAGGGAAGAAAAG AGGAAGGAAGAAAGGAAGGAAAGAAAGAAGGAGAGAACAAAAGGGAGAAAGGGAGGGAAGAAAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:56782265..56782481 26863196 MeRIP-seq:(Medium) rs575778726 Functional Loss SNV dbSNP153 33..33 33 - - - 67857 RMVar_ID_67857 Human_SNP_ID_685192836 m1A Human chr20 + 56805456 56805456 56805456 ACACACTCACAGACACACTGCCTCCCGCACACACTCACACACAGACACATTCACAGACACACACT ACACACTCACAGACACACTGCCTCCCGCACACCCTCACACACAGACACATTCACAGACACACACT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:56805420..56805566 26863196 MeRIP-seq:(Medium) rs925663793 Functional Loss SNV dbSNP153 33..33 33 - - - 67858 RMVar_ID_67858 Human_SNP_ID_685192837 m1A Human chr20 + 56805456 56805456 56805456 ACACACTCACAGACACACTGCCTCCCGCACACACTCACACACAGACACATTCACAGACACACACT ACACACTCACAGACACACTGCCTCCCGCACACTCTCACACACAGACACATTCACAGACACACACT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:56805420..56805566 26863196 MeRIP-seq:(Medium) rs925663793 Functional Loss SNV dbSNP153 33..33 33 - - - 67859 RMVar_ID_67859 Human_SNP_ID_685331013 m1A Human chr20 + 57350905 57350874 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CG________________________________GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1357090213 Functional Loss DEL dbSNP153 3..34 33 - - - 67860 RMVar_ID_67860 Human_SNP_ID_685331039 m1A Human chr20 + 57350905 57350891 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGG_______________GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGGGGCGGGGGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1568772756 Functional Loss DEL dbSNP153 20..34 33 - - - 67861 RMVar_ID_67861 Human_SNP_ID_685331048 m1A Human chr20 + 57350905 57350899 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCG______CGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1475871657 Functional Loss DEL dbSNP153 28..33 33 - - - 67862 RMVar_ID_67862 Human_SNP_ID_685331049 m1A Human chr20 + 57350905 57350900 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGG______GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1163241585 Functional Loss DEL dbSNP153 29..34 33 - - - 67863 RMVar_ID_67863 Human_SNP_ID_685331050 m1A Human chr20 + 57350905 57350901 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGG____CGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1568772794 Functional Loss DEL dbSNP153 30..33 33 - - - 67864 RMVar_ID_67864 Human_SNP_ID_685331051 m1A Human chr20 + 57350905 57350901 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGG_____GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1568772801 Functional Loss DEL dbSNP153 30..34 33 - - - 67865 RMVar_ID_67865 Human_SNP_ID_685331052 m1A Human chr20 + 57350905 57350902 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGG___CGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1568772806 Functional Loss DEL dbSNP153 31..33 33 - - - 67866 RMVar_ID_67866 Human_SNP_ID_685331053 m1A Human chr20 + 57350905 57350902 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGG____GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1568772817 Functional Loss DEL dbSNP153 31..34 33 - - - 67867 RMVar_ID_67867 Human_SNP_ID_685331054 m1A Human chr20 + 57350905 57350903 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGG___GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1167338485 Functional Loss DEL dbSNP153 32..34 33 - - - 67868 RMVar_ID_67868 Human_SNP_ID_685331055 m1A Human chr20 + 57350905 57350903 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGG__CGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1383612660 Functional Loss DEL dbSNP153 32..33 33 - - - 67869 RMVar_ID_67869 Human_SNP_ID_685331056 m1A Human chr20 + 57350905 57350904 57350906 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGG__GGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1375344008 Functional Loss DEL dbSNP153 33..34 33 - - - 67870 RMVar_ID_67870 Human_SNP_ID_685331057 m1A Human chr20 + 57350905 57350904 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGG_CGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1475778630 Functional Loss DEL dbSNP153 33..33 33 - - - 67871 RMVar_ID_67871 Human_SNP_ID_685331065 m1A Human chr20 + 57350905 57350905 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGCCGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1186398981 Functional Loss SNV dbSNP153 33..33 33 - - - 67872 RMVar_ID_67872 Human_SNP_ID_685331066 m1A Human chr20 + 57350905 57350905 57350905 CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGACGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG CGGGGGGCGGGGGGGGCGGGGGGGGCGGGGGGGCGGGGGCGGGGGGCGGGGGGGGGCGGCGCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:57350848..57350937;chr20:57350869..57350954 26863196 MeRIP-seq:(Medium) rs1186398981 Functional Loss SNV dbSNP153 33..33 33 - - - 67873 RMVar_ID_67873 Human_SNP_ID_685333752 m1A Human chr20 - 57359185 57359185 57359185 TACAAAAAAATAAAAGGAACTCAGCAAATCTTACCCCGCCTGTTTACCAAAAACATCACCTCTAG TACAAAAAAATAAAAGGAACTCAGCAAATCTTCCCCCGCCTGTTTACCAAAAACATCACCTCTAG T G MTRNR2L3 Ensembl:ENSG00000256222 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:57358997..57359214;chr20:57359068..57359225;chr20:57358972..57359222;chr20:57359036..57359236 26863196 MeRIP-seq:(Medium) rs967975492 Functional Loss SNV dbSNP153 33..33 33 - - - 67874 RMVar_ID_67874 Human_SNP_ID_685338032 m1A Human chr20 - 57375043 57375043 57375043 CTTGCCTGTGCTTCTGTGCCCAGGAACAGAGCAGCCCGTAATGGCTCACACTGGCCGAGCACTTC CTTGCCTGTGCTTCTGTGCCCAGGAACAGAGCCGCCCGTAATGGCTCACACTGGCCGAGCACTTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:57375016..57375173 26863196 MeRIP-seq:(Medium) rs1387030403 Functional Loss SNV dbSNP153 33..33 33 - - - 67875 RMVar_ID_67875 Human_SNP_ID_685338176 m1A Human chr20 - 57375466 57375466 57375466 GGTGAGCGGGAAAGACACTGCAGGCCACTGGAAGCCCCTCCTATGTGAAGCAGGTGACCTCCCCA GGTGAGCGGGAAAGACACTGCAGGCCACTGGAGGCCCCTCCTATGTGAAGCAGGTGACCTCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:57375439..57375523 26863196 MeRIP-seq:(Medium) rs370280228 Functional Loss SNV dbSNP153 33..33 33 - - - 67876 RMVar_ID_67876 Human_SNP_ID_685342555 m1A Human chr20 + 57391427 57391427 57391427 CGCAGAGTCCCCGCAGCGCCGGTCGGGAGCGCAGCGCGGCGCACGTCGGCGCGCACGGCGGGACG CGCAGAGTCCCCGCAGCGCCGGTCGGGAGCGCCGCGCGGCGCACGTCGGCGCGCACGGCGGGACG A C RBM38 Ensembl:ENSG00000132819 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:57391394..57391707 26863196 MeRIP-seq:(Medium) rs1313923087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659488 67877 RMVar_ID_67877 Human_SNP_ID_685342637 m1A Human chr20 - 57391501 57391501 57391501 ATGGGGGGCGGCGGGGAGCGCGCGGGGCAGCGAGGGGCGCCCGTCCAGCCGCCAGGCCCGACCAC ATGGGGGGCGGCGGGGAGCGCGCGGGGCAGCGCGGGGCGCCCGTCCAGCCGCCAGGCCCGACCAC T G AL109955.1 Ensembl:ENSG00000218018 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:57391401..57391550 26863410 MeRIP-seq:(Medium) rs1206154136 Functional Loss SNV dbSNP153 33..33 33 - - - 67878 RMVar_ID_67878 Human_SNP_ID_685342641 m1A Human chr20 - 57391517 57391517 57391517 GCGCGGGGCTGCGCTCATGGGGGGCGGCGGGGAGCGCGCGGGGCAGCGAGGGGCGCCCGTCCAGC GCGCGGGGCTGCGCTCATGGGGGGCGGCGGGGGGCGCGCGGGGCAGCGAGGGGCGCCCGTCCAGC T C AL109955.1 Ensembl:ENSG00000218018 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:57391401..57391675 26863410 MeRIP-seq:(Medium) rs978972054 Functional Loss SNV dbSNP153 33..33 33 - - - 67879 RMVar_ID_67879 Human_SNP_ID_685342648 m1A Human chr20 + 57391532 57391532 57391532 CTCGCTGCCCCGCGCGCTCCCCGCCGCCCCCCATGAGCGCAGCCCCGCGCGGCCCGGGTCCGTAG CTCGCTGCCCCGCGCGCTCCCCGCCGCCCCCCGTGAGCGCAGCCCCGCGCGGCCCGGGTCCGTAG A G RBM38 Ensembl:ENSG00000132819 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:57391434..57391556 26863196 MeRIP-seq:(Medium) rs1386905015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4654097,Human_RBP_ID_5445798,Human_RBP_ID_9331589 67880 RMVar_ID_67880 Human_SNP_ID_685346099 m1A Human chr20 - 57401597 57401597 57401597 TCTACCTTGCACAATGTCTTCCCCACAAGAGCAGGGTCTCAGCTGCTGCGTCCCAAGTGCCCCAG TCTACCTTGCACAATGTCTTCCCCACAAGAGCCGGGTCTCAGCTGCTGCGTCCCAAGTGCCCCAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:57401587..57401880 26863196 MeRIP-seq:(Medium) rs896304743 Functional Loss SNV dbSNP153 33..33 33 - - - 67881 RMVar_ID_67881 Human_SNP_ID_685346122 m1A Human chr20 - 57401681 57401679 57401681 TGCTTCTTCCCACAGCTCAAAGCTCACCCCTCAGGGGTCCACCCAGGCGGCTCTGTTTCCTTATG TGCTTCTTCCCACAGCTCAAAGCTCACCCCTC__GGGTCCACCCAGGCGGCTCTGTTTCCTTATG CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:57401676..57401823 26863196 MeRIP-seq:(Medium) rs1448291728 Functional Loss DEL dbSNP153 33..34 33 - - - 67882 RMVar_ID_67882 Human_SNP_ID_685346123 m1A Human chr20 - 57401681 57401680 57401681 TGCTTCTTCCCACAGCTCAAAGCTCACCCCTCAGGGGTCCACCCAGGCGGCTCTGTTTCCTTATG TGCTTCTTCCCACAGCTCAAAGCTCACCCCTC_GGGGTCCACCCAGGCGGCTCTGTTTCCTTATG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:57401676..57401823 26863196 MeRIP-seq:(Medium) rs1419616947 Functional Loss DEL dbSNP153 33..33 33 - - - 67883 RMVar_ID_67883 Human_SNP_ID_685346164 m1A Human chr20 + 57401835 57401835 57401835 CGCAGTGCAAGTGGAGATGAGTTAGAAGAGGTAGGTTGAGGCCTAATAACGCAGGAAGCCACAAG CGCAGTGCAAGTGGAGATGAGTTAGAAGAGGTTGGTTGAGGCCTAATAACGCAGGAAGCCACAAG A T RBM38 Ensembl:ENSG00000132819 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:57401727..57401870 26863196 MeRIP-seq:(Medium) rs940809462 Functional Loss SNV dbSNP153 33..33 33 - - - 67884 RMVar_ID_67884 Human_SNP_ID_685348108 m1A Human chr20 + 57407699 57407699 57407699 CAGTACCCACCGGCCACCTATGACCAGTACCCATACGCCGCCTCGCCTGCCACGGCTGCCAGCTT CAGTACCCACCGGCCACCTATGACCAGTACCCTTACGCCGCCTCGCCTGCCACGGCTGCCAGCTT A T RBM38 Ensembl:ENSG00000132819 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:57407601..57407841 26863410 MeRIP-seq:(Medium) rs1242150198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17396647,Human_RBP_ID_26491972,Human_RBP_ID_27023191,Human_RBP_ID_27298823 67885 RMVar_ID_67885 Human_SNP_ID_685348638 m1A Human chr20 + 57409126 57409126 57409126 GCATCCAGGGCTGTGGGGGTCTGGAGGAGGGGACATGAGGTGAGAGGTATCCTGGCCGAGGGCGG GCATCCAGGGCTGTGGGGGTCTGGAGGAGGGGCCATGAGGTGAGAGGTATCCTGGCCGAGGGCGG A C RBM38 Ensembl:ENSG00000132819 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:57409026..57409228;chr20:57409087..57409200 26863196 MeRIP-seq:(Medium) rs1489926379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7015466,Human_RBP_ID_9354039,Human_RBP_ID_9431088,Human_RBP_ID_22081427,Human_RBP_ID_26493175 67886 RMVar_ID_67886 Human_SNP_ID_685369101 m1A Human chr20 - 57488422 57488422 57488422 GAAGATGAAGAGGATGAGGAGGAGGAAGATGAAGAAGATGAAGAAGATGATGATGATGAATAAGT GAAGATGAAGAGGATGAGGAGGAGGAAGATGATGAAGATGAAGAAGATGATGATGATGAATAAGT T A HMGB1P1 Ensembl:ENSG00000124097 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:57488404..57488527 26863196 MeRIP-seq:(Medium) rs1568839002 Functional Loss SNV dbSNP153 33..33 33 - - - 67887 RMVar_ID_67887 Human_SNP_ID_685414596 m1A Human chr20 + 57652528 57652528 57652528 GCAGGTACGGATAGGTGGGCTGGAAGCGGTGGAAGCGCTCCCGCTGGGCGAAGGGCGGCACGGCC GCAGGTACGGATAGGTGGGCTGGAAGCGGTGGGAGCGCTCCCGCTGGGCGAAGGGCGGCACGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:57652481..57652600 26863196 MeRIP-seq:(Medium) rs1224762894 Functional Loss SNV dbSNP153 33..33 33 - - - 67888 RMVar_ID_67888 Human_SNP_ID_685416979 m1A Human chr20 - 57660621 57660621 57660621 TGGAGTATGTAGTGTTGGGGTGTTGTGTGTGTAGGAGTGTTAGGGGTACGTGTTGGGGTGTTATT TGGAGTATGTAGTGTTGGGGTGTTGTGTGTGTGGGAGTGTTAGGGGTACGTGTTGGGGTGTTATT T C PMEPA1 Ensembl:ENSG00000124225 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:57660618..57660919 26863196 MeRIP-seq:(Medium) rs1568964760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76714,RMVar_hsa_circ_211058 67889 RMVar_ID_67889 Human_SNP_ID_685417040 m1A Human chr20 + 57660800 57660797 57660800 CACAACACCCCAACACTCCTACACACACGTCAACAACACTACATACTCCAACACTCCTACACACA CACAACACCCCAACACTCCTACACACACGT___CAACACTACATACTCCAACACTCCTACACACA TCAA T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:57660609..57660901 26863196 MeRIP-seq:(Medium) rs1411164836 Functional Loss DEL dbSNP153 31..33 33 - - - 67890 RMVar_ID_67890 Human_SNP_ID_685419401 m1A Human chr20 - 57668787 57668787 57668787 GAATGGCACGTGCCAGGGTCCTGAGGTGGGTCATGCATGGTGCTTTTATAGAACAGAAAACAAGT GAATGGCACGTGCCAGGGTCCTGAGGTGGGTCGTGCATGGTGCTTTTATAGAACAGAAAACAAGT T C PMEPA1 Ensembl:ENSG00000124225 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:57668783..57668873 26863196 MeRIP-seq:(Medium) rs1160064488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76714,RMVar_hsa_circ_211058 67891 RMVar_ID_67891 Human_SNP_ID_685583676 m1A Human chr20 + 58309865 58309864 58309865 CCGGAGGACGGGCGGCAGCCGCCTCTGCGCGGACCGGGGCTGGGCCGTGCGGCGGCAGCGGCGCC CCGGAGGACGGGCGGCAGCCGCCTCTGCGCGG_CCGGGGCTGGGCCGTGCGGCGGCAGCGGCGCC GA G RAB22A Ensembl:ENSG00000124209 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:58309726..58309924 26863196 MeRIP-seq:(Medium) rs550459560 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4654226,Human_RBP_ID_23004990 RMVar_hsa_circ_211063,RMVar_hsa_circ_94757 67892 RMVar_ID_67892 Human_SNP_ID_685603453 m1A Human chr20 + 58389321 58389321 58389321 ACCGCGTAGACCGACCCCCCCCCAGCGCGCCCACCCGGTAGAGGACCCCCGCCCGTGCCCCGACC ACCGCGTAGACCGACCCCCCCCCAGCGCGCCCCCCCGGTAGAGGACCCCCGCCCGTGCCCCGACC A C VAPB Ensembl:ENSG00000124164 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:58389224..58389358 26863410 MeRIP-seq:(Medium) rs1042509333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659935,Human_RBP_ID_5323294,Human_RBP_ID_18422933 Human_miRNA_ID_2147537,Human_miRNA_ID_2571499,Human_miRNA_ID_2874347,Human_miRNA_ID_2982307,Human_miRNA_ID_2988964,Human_miRNA_ID_3022666,Human_miRNA_ID_3045235 RMVar_hsa_circ_121758,RMVar_hsa_circ_211067 67893 RMVar_ID_67893 Human_SNP_ID_685603454 m1A Human chr20 + 58389321 58389321 58389321 ACCGCGTAGACCGACCCCCCCCCAGCGCGCCCACCCGGTAGAGGACCCCCGCCCGTGCCCCGACC ACCGCGTAGACCGACCCCCCCCCAGCGCGCCCGCCCGGTAGAGGACCCCCGCCCGTGCCCCGACC A G VAPB Ensembl:ENSG00000124164 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:58389224..58389358 26863410 MeRIP-seq:(Medium) rs1042509333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659935,Human_RBP_ID_5323294,Human_RBP_ID_18422933 Human_miRNA_ID_2147537,Human_miRNA_ID_2571499,Human_miRNA_ID_2874347,Human_miRNA_ID_2982307,Human_miRNA_ID_2988964,Human_miRNA_ID_3022666,Human_miRNA_ID_3045235 RMVar_hsa_circ_121758,RMVar_hsa_circ_211067 67894 RMVar_ID_67894 Human_SNP_ID_685603471 m1A Human chr20 + 58389351 58389351 58389351 CCACCCGGTAGAGGACCCCCGCCCGTGCCCCGACCGGTCCCCGCCTTTTTGTAAAACTTAAAGCG CCACCCGGTAGAGGACCCCCGCCCGTGCCCCGGCCGGTCCCCGCCTTTTTGTAAAACTTAAAGCG A G VAPB Ensembl:ENSG00000124164 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr20:58389251..58389400;chr20:58389228..58389421 26863410,26863196 MeRIP-seq:(Medium) rs1346131814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244099,Human_RBP_ID_4659935,Human_RBP_ID_5323294 Human_miRNA_ID_2147538,Human_miRNA_ID_2988965,Human_miRNA_ID_3022667 RMVar_hsa_circ_121758,RMVar_hsa_circ_211067 67895 RMVar_ID_67895 Human_SNP_ID_685603516 m1A Human chr20 + 58389437 58389437 58389437 GCCCCGGTGACCTCTCAGGGGTCTCCCCGCCAAAGGTGCTCCGCCGCTAAGGAACATGGCGAAGG GCCCCGGTGACCTCTCAGGGGTCTCCCCGCCAGAGGTGCTCCGCCGCTAAGGAACATGGCGAAGG A G VAPB Ensembl:ENSG00000124164 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58389218..58389456 26863196 MeRIP-seq:(Medium) rs756028732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660555,Human_RBP_ID_23005223 Human_Splice_Rec_2097555,Human_Splice_Rec_2097565,Human_Splice_Rec_2097569,Human_Splice_Rec_2097575 RMVar_hsa_circ_121758,RMVar_hsa_circ_211067 67896 RMVar_ID_67896 Human_SNP_ID_685607568 m1A Human chr20 + 58405144 58405141 58405145 TTTTAAGTAGGGTAATTAGGGAAGGTCATTTAAGTAGGGTGATTAGGGAAGGTCATTTACCTGAG TTTTAAGTAGGGTAATTAGGGAAGGTCATT____TAGGGTGATTAGGGAAGGTCATTTACCTGAG TTAAG T VAPB Ensembl:ENSG00000124164 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58405142..58405399 26863196 MeRIP-seq:(Medium) rs1450800974 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_14150889 RMVar_hsa_circ_121758,RMVar_hsa_circ_211067 67897 RMVar_ID_67897 Human_SNP_ID_685618816 m1A Human chr20 - 58446836 58446836 58446836 TCTCCAAGTCCTCCAGGAGCCACGCGTGCTCCACATTCTTTCTTTTCCTGGCACATTTTTGGCTG TCTCCAAGTCCTCCAGGAGCCACGCGTGCTCCTCATTCTTTCTTTTCCTGGCACATTTTTGGCTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58446789..58446878 26863196 MeRIP-seq:(Medium) rs938574461 Functional Loss SNV dbSNP153 33..33 33 - - - 67898 RMVar_ID_67898 Human_SNP_ID_685618838 m1A Human chr20 + 58446912 58446909 58446913 TTAGGGTGTTTTCCCTAGAATTACATAATGAAAAAAAGAATAAGGCAAAGAGGAGGTGAATATGG TTAGGGTGTTTTCCCTAGAATTACATAATG____AAAGAATAAGGCAAAGAGGAGGTGAATATGG GAAAA G VAPB Ensembl:ENSG00000124164 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58446861..58447008 26863196 MeRIP-seq:(Medium) rs998823824 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_2691219,Human_RBP_ID_14152292,Human_RBP_ID_18775893 RMVar_hsa_circ_76559,RMVar_hsa_circ_211074 67899 RMVar_ID_67899 Human_SNP_ID_685632006 m1A Human chr20 + 58497216 58497216 58497216 GAAAGGGGCCTCCTGGGGGTGAGGGGGCATGCAGCGGGTGGAGGCTGAGGGGCAGATGCGGGTTT GAAAGGGGCCTCCTGGGGGTGAGGGGGCATGCGGCGGGTGGAGGCTGAGGGGCAGATGCGGGTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58497153..58497218 26863196 MeRIP-seq:(Medium) rs918636297 Functional Loss SNV dbSNP153 33..33 33 - - - 67900 RMVar_ID_67900 Human_SNP_ID_685637644 m1A Human chr20 + 58520240 58520216 58520240 GATGAGTGGGGGGATGGATGGATAGATGGATGAATGGGTGAATGGGTGGGTGGATGGATAGATGG GATGAGTGG________________________ATGGGTGAATGGGTGGGTGGATGGATAGATGG GGGGGATGGATGGATAGATGGATGA G APCDD1L-DT Ensembl:ENSG00000231290 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58520174..58520290 26863196 MeRIP-seq:(Medium) rs1568760607 Functional Loss DEL dbSNP153 10..33 33 - - - RMVar_hsa_circ_10753,RMVar_hsa_circ_280335,RMVar_hsa_circ_211075 67901 RMVar_ID_67901 Human_SNP_ID_685637662 m1A Human chr20 + 58520240 58520240 58520240 GATGAGTGGGGGGATGGATGGATAGATGGATGAATGGGTGAATGGGTGGGTGGATGGATAGATGG GATGAGTGGGGGGATGGATGGATAGATGGATGGATGGGTGAATGGGTGGGTGGATGGATAGATGG A G APCDD1L-DT Ensembl:ENSG00000231290 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58520174..58520290 26863196 MeRIP-seq:(Medium) rs1217391302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10753,RMVar_hsa_circ_280335,RMVar_hsa_circ_211075 67902 RMVar_ID_67902 Human_SNP_ID_685637684 m1A Human chr20 - 58520266 58520263 58520267 TTCCATTCACCCACTCACTCATCCATCCATCTATCCATCCACCCACCCATTCACCCATTCATCCA TTCCATTCACCCACTCACTCATCCATCCATC____CATCCACCCACCCATTCACCCATTCATCCA GGATA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58520177..58520318 26863196 MeRIP-seq:(Medium) rs1337221263 Functional Loss DEL dbSNP153 32..35 33 - - - 67903 RMVar_ID_67903 Human_SNP_ID_685653795 m1A Human chr20 + 58586532 58586532 58586532 TCCATAAGGGCTGCCTCCCAAAGCGCTCTCCCACCATTCTCATCTCAGGGCTTGCTTCTGGGGAC TCCATAAGGGCTGCCTCCCAAAGCGCTCTCCCGCCATTCTCATCTCAGGGCTTGCTTCTGGGGAC A G APCDD1L-DT Ensembl:ENSG00000231290 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58586501..58586550 26863196 MeRIP-seq:(Medium) rs1169642830 Functional Loss SNV dbSNP153 33..33 33 - - - 67904 RMVar_ID_67904 Human_SNP_ID_685670515 m1A Human chr20 - 58651281 58651281 58651281 CTCTTCTCCGGCTCCCTCCATCCCCGGATCTGACTGCAGCTCAGCCCCGGACCGTTTCCGTGCTG CTCTTCTCCGGCTCCCTCCATCCCCGGATCTGCCTGCAGCTCAGCCCCGGACCGTTTCCGTGCTG T G lnc-APCDD1L-3-002 RNACentral:URS0000D5D2F6 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58651274..58651450 26863196 MeRIP-seq:(Medium) rs949953702 Functional Loss SNV dbSNP153 33..33 33 - - - 67905 RMVar_ID_67905 Human_SNP_ID_685670526 m1A Human chr20 + 58651312 58651310 58651313 GTCAGATCCGGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGAAGGCCGGGGAGGCAGGCCCTGCT GTCAGATCCGGGGATGGAGGGAGCCGGAGAA___GAGTGAGAAGGCCGGGGAGGCAGGCCCTGCT AGAG A STX16 Ensembl:ENSG00000124222 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58651251..58652045 26863196 MeRIP-seq:(Medium) rs552143347 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_244816,Human_RBP_ID_779857,Human_RBP_ID_7016440,Human_RBP_ID_9389574,Human_RBP_ID_18422934,Human_RBP_ID_19006052,Human_RBP_ID_23004791,Human_RBP_ID_23119698,Human_RBP_ID_26343158,Human_RBP_ID_27819944 Human_Splice_Rec_2097805 67906 RMVar_ID_67906 Human_SNP_ID_685670527 m1A Human chr20 + 58651312 58651312 58651312 GTCAGATCCGGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGAAGGCCGGGGAGGCAGGCCCTGCT GTCAGATCCGGGGATGGAGGGAGCCGGAGAAGTGGAGTGAGAAGGCCGGGGAGGCAGGCCCTGCT A T STX16 Ensembl:ENSG00000124222 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58651251..58652045 26863196 MeRIP-seq:(Medium) rs1163918191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244816,Human_RBP_ID_779857,Human_RBP_ID_7016440,Human_RBP_ID_9389574,Human_RBP_ID_18422934,Human_RBP_ID_19006052,Human_RBP_ID_23004791,Human_RBP_ID_23119698,Human_RBP_ID_26343158,Human_RBP_ID_27819944 Human_Splice_Rec_2097805 67907 RMVar_ID_67907 Human_SNP_ID_685670533 m1A Human chr20 + 58651321 58651321 58651321 GGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGAAGGCCGGGGAGGCAGGCCCTGCTGTCTTCCTG GGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGGAGGCCGGGGAGGCAGGCCCTGCTGTCTTCCTG A G STX16 Ensembl:ENSG00000124222 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr20:58651301..58651425;chr20:58651251..58652036 26863196 MeRIP-seq:(Medium) rs1450302607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244816,Human_RBP_ID_779857,Human_RBP_ID_4665222,Human_RBP_ID_9389574,Human_RBP_ID_18422934,Human_RBP_ID_19006052,Human_RBP_ID_22259859,Human_RBP_ID_23004791,Human_RBP_ID_23119698,Human_RBP_ID_26343158,Human_RBP_ID_27819944 Human_Splice_Rec_2097685,Human_Splice_Rec_2097711,Human_Splice_Rec_2097805 67908 RMVar_ID_67908 Human_SNP_ID_685674462 m1A Human chr20 - 58667998 58667998 58667998 AATTCTTTCATCTTCTGCTTAATCCGGCCAACATCATACTGAATCTAAGCAAATGAAGTCACAGA AATTCTTTCATCTTCTGCTTAATCCGGCCAACGTCATACTGAATCTAAGCAAATGAAGTCACAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58667994..58668109 26863196 MeRIP-seq:(Medium) rs746280542 Functional Loss SNV dbSNP153 33..33 33 - - - 67909 RMVar_ID_67909 Human_SNP_ID_685674836 m1A Human chr20 - 58669444 58669444 58669444 CACTAGGCCCGGGCAGCACTCACGTTTGAGGTAGCCTGACTGTGCGTGCCGGAAGCTGGTGGAGA CACTAGGCCCGGGCAGCACTCACGTTTGAGGTGGCCTGACTGTGCGTGCCGGAAGCTGGTGGAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58668098..58671269 32194978 MeRIP-seq:(Medium) rs1414917150 Functional Loss SNV dbSNP153 33..33 33 - - - 67910 RMVar_ID_67910 Human_SNP_ID_685676627 m1A Human chr20 - 58676266 58676266 58676266 ATGCCACTTATCGAGACTTCACGCCAACGAGGACAACAATGAGCACAATGATGATGACAAATAAT ATGCCACTTATCGAGACTTCACGCCAACGAGGGCAACAATGAGCACAATGATGATGACAAATAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58676260..58676407 26863196 MeRIP-seq:(Medium) rs771938906 Functional Loss SNV dbSNP153 33..33 33 - - - 67911 RMVar_ID_67911 Human_SNP_ID_685677078 m1A Human chr20 + 58678076 58678076 58678076 GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCATCTGATTTTAACCCATGGTTGAGACGTTCCAA GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCGTCTGATTTTAACCCATGGTTGAGACGTTCCAA A G STX16-NPEPL1,STX16 Ensembl:ENSG00000254995,Ensembl:ENSG00000124222 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6128397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1099734,Human_RBP_ID_8856526,Human_RBP_ID_14154359,Human_RBP_ID_17396245,Human_RBP_ID_17512474,Human_RBP_ID_22817880 GWAS_ID_8117,GWAS_ID_8118,GWAS_ID_8119,GWAS_ID_8120,GWAS_ID_8121,GWAS_ID_8122,GWAS_ID_8123,GWAS_ID_8124 RMVar_hsa_circ_211076,RMVar_hsa_circ_125383,RMVar_hsa_circ_264814 67912 RMVar_ID_67912 Human_SNP_ID_685677079 m1A Human chr20 + 58678076 58678076 58678076 GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCATCTGATTTTAACCCATGGTTGAGACGTTCCAA GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCTTCTGATTTTAACCCATGGTTGAGACGTTCCAA A T STX16-NPEPL1,STX16 Ensembl:ENSG00000254995,Ensembl:ENSG00000124222 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6128397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1099734,Human_RBP_ID_8856526,Human_RBP_ID_14154359,Human_RBP_ID_17396245,Human_RBP_ID_17512474,Human_RBP_ID_22817880 GWAS_ID_8117,GWAS_ID_8118,GWAS_ID_8119,GWAS_ID_8120,GWAS_ID_8121,GWAS_ID_8122,GWAS_ID_8123,GWAS_ID_8124 RMVar_hsa_circ_211076,RMVar_hsa_circ_125383,RMVar_hsa_circ_264814 67913 RMVar_ID_67913 Human_SNP_ID_685677380 m1A Human chr20 - 58679064 58679064 58679064 AACGCGTGGTAAACATGTCTGTTTCTCCTTCTACCTCCACTCAACCTGAGCTGCACCCGGACACT AACGCGTGGTAAACATGTCTGTTTCTCCTTCTGCCTCCACTCAACCTGAGCTGCACCCGGACACT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58678675..58679076 32194978 MeRIP-seq:(Medium) rs1055878524 Functional Loss SNV dbSNP153 33..33 33 - - - 67914 RMVar_ID_67914 Human_SNP_ID_685681030 m1A Human chr20 - 58692697 58692697 58692697 GGGCGCGAGGGGGCGCCGGCCAGGCCGGGCGGAAGGGTGCGGGCAGGCCCGGCCGGGCAGGCCCG GGGCGCGAGGGGGCGCCGGCCAGGCCGGGCGGTAGGGTGCGGGCAGGCCCGGCCGGGCAGGCCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58692690..58693113 26863196 MeRIP-seq:(Medium) rs893865070 Functional Loss SNV dbSNP153 33..33 33 - - - 67915 RMVar_ID_67915 Human_SNP_ID_685681064 m1A Human chr20 - 58692792 58692792 58692792 CCGGCCTCGGCACCGCCCCGGCCCTGCCCGGCAGCCCGCGGGCCCCGCCTCCCCCGCCGCTCCGG CCGGCCTCGGCACCGCCCCGGCCCTGCCCGGCTGCCCGCGGGCCCCGCCTCCCCCGCCGCTCCGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:58692783..58693050 26863196 MeRIP-seq:(Medium) rs1169560516 Functional Loss SNV dbSNP153 33..33 33 - - - 67916 RMVar_ID_67916 Human_SNP_ID_685681138 m1A Human chr20 + 58692895 58692895 58692895 CCGGGCCGGGCAGGGCCGGGGCGTGGGCCGGCAGGAAGATGGCGAACGTGGGGCTGCAGTTCCAG CCGGGCCGGGCAGGGCCGGGGCGTGGGCCGGCGGGAAGATGGCGAACGTGGGGCTGCAGTTCCAG A G STX16-NPEPL1,NPEPL1 Ensembl:ENSG00000254995,Ensembl:ENSG00000215440 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:58692200..58694550;chr20:58692200..58694639;chr20:58692712..58693492 26863196 MeRIP-seq:(Medium) rs1016312706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5385447,Human_RBP_ID_18463073,Human_RBP_ID_19110058,Human_RBP_ID_21983042,Human_RBP_ID_26788544 RMVar_hsa_circ_319974,RMVar_hsa_circ_357573 67917 RMVar_ID_67917 Human_SNP_ID_685681359 m1A Human chr20 + 58693497 58693497 58693497 CCTATCCGAGTGTTGGAAGCAAAGCAGCCCCCAGCCTGGCCCTTCCAGGCTTGGTGGCTTCATCC CCTATCCGAGTGTTGGAAGCAAAGCAGCCCCCCGCCTGGCCCTTCCAGGCTTGGTGGCTTCATCC A C STX16-NPEPL1,NPEPL1 Ensembl:ENSG00000254995,Ensembl:ENSG00000215440 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58693491..58693691 32194978 MeRIP-seq:(Medium) rs1213278228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319974,RMVar_hsa_circ_357573 67918 RMVar_ID_67918 Human_SNP_ID_685682013 m1A Human chr20 - 58695033 58695033 58695033 ATGCACACACCAGCAAACATACACAGCAACACATACCACACACACACACACATCACACATGCACA ATGCACACACCAGCAAACATACACAGCAACACGTACCACACACACACACACATCACACATGCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58695028..58695136 26863196 MeRIP-seq:(Medium) rs1381678841 Functional Loss SNV dbSNP153 33..33 33 - - - 67919 RMVar_ID_67919 Human_SNP_ID_685682017 m1A Human chr20 - 58695035 58695035 58695035 TCATGCACACACCAGCAAACATACACAGCAACACATACCACACACACACACACATCACACATGCA TCATGCACACACCAGCAAACATACACAGCAACTCATACCACACACACACACACATCACACATGCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58695028..58695134 26863196 MeRIP-seq:(Medium) rs1298732707 Functional Loss SNV dbSNP153 33..33 33 - - - 67920 RMVar_ID_67920 Human_SNP_ID_685682022 m1A Human chr20 - 58695041 58695041 58695041 CACCACTCATGCACACACCAGCAAACATACACAGCAACACATACCACACACACACACACATCACA CACCACTCATGCACACACCAGCAAACATACACCGCAACACATACCACACACACACACACATCACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58695035..58695162 26863196 MeRIP-seq:(Medium) rs1229603712 Functional Loss SNV dbSNP153 33..33 33 - - - 67921 RMVar_ID_67921 Human_SNP_ID_685682171 m1A Human chr20 + 58695217 58695217 58695217 TGTTGTGTGTGAGTACTGGTGTGTGCATGAGCAGCATGTGTTGCTGTGTGTATGAGTGCTGGTGT TGTTGTGTGTGAGTACTGGTGTGTGCATGAGCGGCATGTGTTGCTGTGTGTATGAGTGCTGGTGT A G STX16-NPEPL1,NPEPL1 Ensembl:ENSG00000254995,Ensembl:ENSG00000215440 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58695214..58695326 26863196 MeRIP-seq:(Medium) rs373668116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5296780,Human_RBP_ID_5652403,Human_RBP_ID_23115347,Human_RBP_ID_23918017 RMVar_hsa_circ_41873,RMVar_hsa_circ_319974,RMVar_hsa_circ_321298,RMVar_hsa_circ_126254,RMVar_hsa_circ_211081 67922 RMVar_ID_67922 Human_SNP_ID_685682203 m1A Human chr20 - 58695275 58695271 58695275 ACTAGCACTCATACACACACAGCAACACACACAACACACACACACACCACTCATGCACACACCAG ACTAGCACTCATACACACACAGCAACACACAC____CACACACACACCACTCATGCACACACCAG GTGTT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:58695267..58695396 26863196 MeRIP-seq:(Medium) rs796582039 Functional Loss DEL dbSNP153 33..36 33 - - - 67923 RMVar_ID_67923 Human_SNP_ID_685682207 m1A Human chr20 - 58695275 58695275 58695275 ACTAGCACTCATACACACACAGCAACACACACAACACACACACACACCACTCATGCACACACCAG ACTAGCACTCATACACACACAGCAACACACACCACACACACACACACCACTCATGCACACACCAG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:58695267..58695396 26863196 MeRIP-seq:(Medium) rs370014208 Functional Loss SNV dbSNP153 33..33 33 - - - 67924 RMVar_ID_67924 Human_SNP_ID_685683818 m1A Human chr20 + 58701053 58701053 58701053 TATGGGGTTGGCAAAGCCGCCCTGCATCCCCCAGCCCTGGCCGTCCTCAGCCACACCCCAGATGG TATGGGGTTGGCAAAGCCGCCCTGCATCCCCCGGCCCTGGCCGTCCTCAGCCACACCCCAGATGG A G STX16-NPEPL1,NPEPL1 Ensembl:ENSG00000254995,Ensembl:ENSG00000215440 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58701048..58701205 26863196 MeRIP-seq:(Medium) rs1478922953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779255,Human_RBP_ID_8235018,Human_RBP_ID_9391031,Human_RBP_ID_18167712,Human_RBP_ID_19006069,Human_RBP_ID_26342510 Human_Splice_Rec_2097952,Human_Splice_Rec_2097980,Human_Splice_Rec_2098004,Human_Splice_Rec_2098026,Human_Splice_Rec_2098046,Human_Splice_Rec_2098058,Human_Splice_Rec_2098078 RMVar_hsa_circ_92740,RMVar_hsa_circ_41873,RMVar_hsa_circ_321298,RMVar_hsa_circ_110168,RMVar_hsa_circ_126254,RMVar_hsa_circ_211081,RMVar_hsa_circ_93269,RMVar_hsa_circ_211082,RMVar_hsa_circ_211083,RMVar_hsa_circ_211084 67925 RMVar_ID_67925 Human_SNP_ID_685687694 m1A Human chr20 + 58713402 58713402 58713402 AGTGTCCCAGGAAATCCCGTCCCTGAGCGGGGATCTCTACCATGCCCCAGGACGGTGGAAATCAA AGTGTCCCAGGAAATCCCGTCCCTGAGCGGGGGTCTCTACCATGCCCCAGGACGGTGGAAATCAA A G STX16-NPEPL1,NPEPL1 Ensembl:ENSG00000254995,Ensembl:ENSG00000215440 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58713397..58713544 26863196 MeRIP-seq:(Medium) rs1172106922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926109,Human_RBP_ID_5119409,Human_RBP_ID_5383968,Human_RBP_ID_19106857,Human_RBP_ID_22549400 RMVar_hsa_circ_321298,RMVar_hsa_circ_31801 67926 RMVar_ID_67926 Human_SNP_ID_685687823 m1A Human chr20 - 58713749 58713749 58713749 CAGGCAGAAAGGACCATGGCCATGAAGCACACAGGAGGCGGTTCCCGGCTCTGCATCCAGCCTGG CAGGCAGAAAGGACCATGGCCATGAAGCACACTGGAGGCGGTTCCCGGCTCTGCATCCAGCCTGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58713607..58713758 32194978 MeRIP-seq:(Medium) rs1408922681 Functional Loss SNV dbSNP153 33..33 33 - - - 67927 RMVar_ID_67927 Human_SNP_ID_685705953 m1A Human chr20 - 58786098 58786094 58786098 CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGAGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGG____GGGTGGTGCAAAACTGCCCGTGGCTGCGA CACCT C lnc-CTSZ-11 RNACentral:URS00008B87ED lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58786076..58786150 26863196 MeRIP-seq:(Medium) rs1568885488 Functional Loss DEL dbSNP153 33..36 33 - - - 67928 RMVar_ID_67928 Human_SNP_ID_685705954 m1A Human chr20 - 58786098 58786095 58786098 CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGAGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGG___TGGGTGGTGCAAAACTGCCCGTGGCTGCGA ACCT A lnc-CTSZ-11 RNACentral:URS00008B87ED lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58786076..58786150 26863196 MeRIP-seq:(Medium) rs1568885496 Functional Loss DEL dbSNP153 33..35 33 - - - 67929 RMVar_ID_67929 Human_SNP_ID_685705960 m1A Human chr20 - 58786098 58786096 58786098 CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGAGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGG__GTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCT C lnc-CTSZ-11 RNACentral:URS00008B87ED lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58786076..58786150 26863196 MeRIP-seq:(Medium) rs1568885498 Functional Loss DEL dbSNP153 33..34 33 - - - 67930 RMVar_ID_67930 Human_SNP_ID_685705962 m1A Human chr20 - 58786098 58786097 58786098 CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGAGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGG_GGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CT C lnc-CTSZ-11 RNACentral:URS00008B87ED lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58786076..58786150 26863196 MeRIP-seq:(Medium) rs1423880940 Functional Loss DEL dbSNP153 33..33 33 - - - 67931 RMVar_ID_67931 Human_SNP_ID_685705964 m1A Human chr20 - 58786098 58786098 58786098 CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGAGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA CCGGGGGGGGGGGGGGGGGGGGCGGGGGGTGGGGGTGGGTGGTGCAAAACTGCCCGTGGCTGCGA T C lnc-CTSZ-11 RNACentral:URS00008B87ED lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58786076..58786150 26863196 MeRIP-seq:(Medium) rs1220472638 Functional Loss SNV dbSNP153 33..33 33 - - - 67932 RMVar_ID_67932 Human_SNP_ID_685716820 m1A Human chr20 - 58828997 58828863 58828998 GGGGCCAGGAGCTCTGCCATGTTGAGTGGGGCAGTGGGGCCAGGAGCTCTGCCATGTTGAGTGGG GGGGCCAGGAGCTCTGCCATGTTGAGTGGGG__________________________________ ACTCAACATGGCAGAGCTCCTGGCCCCACCGCCCCACTCAACATGGCAGAGCTCCTGGCCCCACCGCCCCACTCAACATGGCAGAGCTCCTGGCCCCACCGCCCCACTCAACATGGCAGAGCTCCTGGCCCCACTG A GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58828996..58829248 26863196 MeRIP-seq:(Medium) rs1568899426 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_7016934 67933 RMVar_ID_67933 Human_SNP_ID_685716857 m1A Human chr20 - 58828997 58828997 58828997 GGGGCCAGGAGCTCTGCCATGTTGAGTGGGGCAGTGGGGCCAGGAGCTCTGCCATGTTGAGTGGG GGGGCCAGGAGCTCTGCCATGTTGAGTGGGGCGGTGGGGCCAGGAGCTCTGCCATGTTGAGTGGG T C GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58828996..58829248 26863196 MeRIP-seq:(Medium) rs866433998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7016934 67934 RMVar_ID_67934 Human_SNP_ID_685717188 m1A Human chr20 - 58830339 58830295 58830339 GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTGATGGTGGTGGTGATGATGATGGTGTGGTGGTGG GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTG_________________________________ CCACCATCACCACCACCACCACACCATCATCATCACCACCACCAT C GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58830337..58830517 26863196 MeRIP-seq:(Medium) rs1378156492 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5652405,Human_RBP_ID_23913425 67935 RMVar_ID_67935 Human_SNP_ID_685717229 m1A Human chr20 - 58830339 58830339 58830339 GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTGATGGTGGTGGTGATGATGATGGTGTGGTGGTGG GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTGGTGGTGGTGGTGATGATGATGGTGTGGTGGTGG T C GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58830337..58830517 26863196 MeRIP-seq:(Medium) rs897778410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5652405,Human_RBP_ID_23913425 67936 RMVar_ID_67936 Human_SNP_ID_685722284 m1A Human chr20 + 58849554 58849550 58849555 CCCAGAAAATGGGCTGCAAAAATCTCCATCCCAACTGCCCAAAGTTCCTTAATCTGCCATGTCTA CCCAGAAAATGGGCTGCAAAAATCTCCAT_____CTGCCCAAAGTTCCTTAATCTGCCATGTCTA TCCCAA T GNAS Ensembl:ENSG00000087460 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58849550..58849639 26863196 MeRIP-seq:(Medium) rs1421745116 Functional Loss DEL dbSNP153 30..34 33 - - - 67937 RMVar_ID_67937 Human_SNP_ID_685722287 m1A Human chr20 + 58849554 58849554 58849554 CCCAGAAAATGGGCTGCAAAAATCTCCATCCCAACTGCCCAAAGTTCCTTAATCTGCCATGTCTA CCCAGAAAATGGGCTGCAAAAATCTCCATCCCCACTGCCCAAAGTTCCTTAATCTGCCATGTCTA A C GNAS Ensembl:ENSG00000087460 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58849550..58849639 26863196 MeRIP-seq:(Medium) rs945001614 Functional Loss SNV dbSNP153 33..33 33 - - - 67938 RMVar_ID_67938 Human_SNP_ID_685722288 m1A Human chr20 + 58849554 58849554 58849554 CCCAGAAAATGGGCTGCAAAAATCTCCATCCCAACTGCCCAAAGTTCCTTAATCTGCCATGTCTA CCCAGAAAATGGGCTGCAAAAATCTCCATCCCGACTGCCCAAAGTTCCTTAATCTGCCATGTCTA A G GNAS Ensembl:ENSG00000087460 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58849550..58849639 26863196 MeRIP-seq:(Medium) rs945001614 Functional Loss SNV dbSNP153 33..33 33 - - - 67939 RMVar_ID_67939 Human_SNP_ID_685732307 m1A Human chr20 - 58889234 58889234 58889234 CCGCGCCGCAGCCCGGAGCCAGAGAGCAGGGGAGCGCCGCGCCGGCCAGCCACCTGACGCAGCCC CCGCGCCGCAGCCCGGAGCCAGAGAGCAGGGGCGCGCCGCGCCGGCCAGCCACCTGACGCAGCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:58889126..58891125;chr20:58889126..58889580;chr20:58889126..58891061;chr20:58889126..58891025 26863196 MeRIP-seq:(Medium) rs767001623 Functional Loss SNV dbSNP153 33..33 33 - - - 67940 RMVar_ID_67940 Human_SNP_ID_685732354 m1A Human chr20 - 58889323 58889323 58889323 ACATGTGAGTGAGGTGCACTCACACGCAAGGCAGCGCCTGCCGGCCGCCCGCCGCCGCCCCGCGC ACATGTGAGTGAGGTGCACTCACACGCAAGGCTGCGCCTGCCGGCCGCCCGCCGCCGCCCCGCGC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:58889183..58889425 26863410 MeRIP-seq:(Medium) rs1370563095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8537136 67941 RMVar_ID_67941 Human_SNP_ID_685732359 m1A Human chr20 - 58889332 58889330 58889332 CCCCGACTTACATGTGAGTGAGGTGCACTCACACGCAAGGCAGCGCCTGCCGGCCGCCCGCCGCC CCCCGACTTACATGTGAGTGAGGTGCACTCAC__GCAAGGCAGCGCCTGCCGGCCGCCCGCCGCC CGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58889126..58889450 26863196 MeRIP-seq:(Medium) rs915223141 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8537136 67942 RMVar_ID_67942 Human_SNP_ID_685732362 m1A Human chr20 + 58889350 58889350 58889350 GGCGCTGCCTTGCGTGTGAGTGCACCTCACTCACATGTAAGTCGGGGAGCGCCGGGGCCTCCCGC GGCGCTGCCTTGCGTGTGAGTGCACCTCACTCGCATGTAAGTCGGGGAGCGCCGGGGCCTCCCGC A G GNAS Ensembl:ENSG00000087460 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58889197..58889498 32194978 MeRIP-seq:(Medium) rs903125078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1304792,Human_RBP_ID_4659937,Human_RBP_ID_5445815,Human_RBP_ID_8942844 Human_Splice_Rec_2098495,Human_Splice_Rec_2098525,Human_Splice_Rec_2098565,Human_Splice_Rec_2098585,Human_Splice_Rec_2098607,Human_Splice_Rec_2098627 67943 RMVar_ID_67943 Human_SNP_ID_685733437 m1A Human chr20 - 58891453 58891453 58891453 GGCCGAGGGGGCTGATGGCCGCCGCCGGGCCGAGGCGGACCAGAGCAGGAGCTGCGGGAGCTGCT GGCCGAGGGGGCTGATGGCCGCCGCCGGGCCGCGGCGGACCAGAGCAGGAGCTGCGGGAGCTGCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58891351..58891904 26863196 MeRIP-seq:(Medium) rs1367169402 Functional Loss SNV dbSNP153 33..33 33 - - - 67944 RMVar_ID_67944 Human_SNP_ID_685733459 m1A Human chr20 - 58891491 58891491 58891491 ACCGAGGGGCGCGCGCAGCTCCCCGCCCCTCGAGCCGAGGCCGAGGGGGCTGATGGCCGCCGCCG ACCGAGGGGCGCGCGCAGCTCCCCGCCCCTCGCGCCGAGGCCGAGGGGGCTGATGGCCGCCGCCG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:58891076..58891900 26863410 MeRIP-seq:(Medium) rs1462475357 Functional Loss SNV dbSNP153 33..33 33 - - - 67945 RMVar_ID_67945 Human_SNP_ID_685733461 m1A Human chr20 + 58891494 58891494 58891494 CGGCGGCCATCAGCCCCCTCGGCCTCGGCTCGAGGGGCGGGGAGCTGCGCGCGCCCCTCGGTCCG CGGCGGCCATCAGCCCCCTCGGCCTCGGCTCGGGGGGCGGGGAGCTGCGCGCGCCCCTCGGTCCG A G GNAS Ensembl:ENSG00000087460 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr20:58891401..58891751 26863410 MeRIP-seq:(Medium) rs1167645241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63376,Human_RBP_ID_149782,Human_RBP_ID_244694,Human_RBP_ID_567441,Human_RBP_ID_831342,Human_RBP_ID_4654678,Human_RBP_ID_5503614,Human_RBP_ID_9331602,Human_RBP_ID_18951755 67946 RMVar_ID_67946 Human_SNP_ID_685733465 m1A Human chr20 + 58891504 58891504 58891504 CAGCCCCCTCGGCCTCGGCTCGAGGGGCGGGGAGCTGCGCGCGCCCCTCGGTCCGACCGACACCC CAGCCCCCTCGGCCTCGGCTCGAGGGGCGGGGGGCTGCGCGCGCCCCTCGGTCCGACCGACACCC A G GNAS Ensembl:ENSG00000087460 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEK293T,untreat control chr20:58891351..58891859;chr20:58891326..58891850;chr20:58891207..58891783;chr20:58891181..58891789 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs963712201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149782,Human_RBP_ID_244694,Human_RBP_ID_567441,Human_RBP_ID_779625,Human_RBP_ID_4654678,Human_RBP_ID_5503614,Human_RBP_ID_9331602,Human_RBP_ID_18951755 67947 RMVar_ID_67947 Human_SNP_ID_685733656 m1A Human chr20 - 58891786 58891786 58891786 TGCAGCTGCTTCTCGATCTTTTTGTTGGCCTCACGCTGCGCCTTCTCCTCGTTGCGCTGGTCCTC TGCAGCTGCTTCTCGATCTTTTTGTTGGCCTCGCGCTGCGCCTTCTCCTCGTTGCGCTGGTCCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:58891672..58891911 26863196 MeRIP-seq:(Medium) rs1391764576 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 67948 RMVar_ID_67948 Human_SNP_ID_685733688 m1A Human chr20 - 58891854 58891852 58891855 GCGCCCCCCGCCCGCCCTTACCCAGCAGCAGCAGGCGGTGCGTGGCCCGGTAGACCTGCTTGTCC GCGCCCCCCGCCCGCCCTTACCCAGCAGCAG___GCGGTGCGTGGCCCGGTAGACCTGCTTGTCC CCTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58891351..58892016 32194978 MeRIP-seq:(Medium) rs774711025 Functional Loss DEL dbSNP153 32..34 33 - - - 67949 RMVar_ID_67949 Human_SNP_ID_685733850 m1A Human chr20 - 58892095 58892089 58892095 GAGACACTGAGCGGGCAGGCCGGGGGAGGGGGACCCGCGCCCGCGTCGCCACGGCCCCCCGCCCC GAGACACTGAGCGGGCAGGCCGGGGGAGGGGG______GCCCGCGTCGCCACGGCCCCCCGCCCC CGCGGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58892093..58892535 26863196 MeRIP-seq:(Medium) rs1177920419 Functional Loss DEL dbSNP153 33..38 33 - - - 67950 RMVar_ID_67950 Human_SNP_ID_685734166 m1A Human chr20 + 58892674 58892674 58892674 TGTGTGTGCGCGGAGCAGACGTGTCCCGGGCCAGGCCGGGCCGTGGAAGGAGGAGAAGGAGAGTC TGTGTGTGCGCGGAGCAGACGTGTCCCGGGCCGGGCCGGGCCGTGGAAGGAGGAGAAGGAGAGTC A G GNAS Ensembl:ENSG00000087460 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58892670..58892819 32194978 MeRIP-seq:(Medium) rs535938655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63385,Human_RBP_ID_264547,Human_RBP_ID_779630,Human_RBP_ID_831297,Human_RBP_ID_1068360,Human_RBP_ID_3654367,Human_RBP_ID_5200771,Human_RBP_ID_5322983,Human_RBP_ID_8113479,Human_RBP_ID_8204659,Human_RBP_ID_9430861,Human_RBP_ID_10024292,Human_RBP_ID_17143152,Human_RBP_ID_17208264,Human_RBP_ID_21984114,Human_RBP_ID_22700876,Human_RBP_ID_23003847,Human_RBP_ID_23918018,Human_RBP_ID_26787725 67951 RMVar_ID_67951 Human_SNP_ID_685735189 m1A Human chr20 - 58895604 58895604 58895604 GTGCTTTTACCAGATTCTCCAGCACCTAGAAAATGAAAGTAAGTCTCAGGTTATGAAGGAGGCAT GTGCTTTTACCAGATTCTCCAGCACCTAGAAAGTGAAAGTAAGTCTCAGGTTATGAAGGAGGCAT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:58895601..58895650 26863196 MeRIP-seq:(Medium) rs1435447192 Functional Loss SNV dbSNP153 33..33 33 - - - 67952 RMVar_ID_67952 Human_SNP_ID_685735198 m1A Human chr20 - 58895667 58895667 58895667 AGATTTGACACTTACTCTCCATTAAACCCATTAACATGCAGGATCCTCATCTGCTTCACAATGGT AGATTTGACACTTACTCTCCATTAAACCCATTGACATGCAGGATCCTCATCTGCTTCACAATGGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:58895601..58895675 26863196 MeRIP-seq:(Medium) rs1385345384 Functional Loss SNV dbSNP153 33..33 33 - - - 67953 RMVar_ID_67953 Human_SNP_ID_685737798 m1A Human chr20 + 58903551 58903551 58903551 ATCCCACTGCAGTGAGAAGGCAACCAAAGTGCAGGACATCAAAAACAACCTGAAAGAGGCGATTG ATCCCACTGCAGTGAGAAGGCAACCAAAGTGCGGGACATCAAAAACAACCTGAAAGAGGCGATTG A G GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:58903526..58903826;chr20:58903526..58903575 26863196 MeRIP-seq:(Medium) rs1216764349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62047,Human_RBP_ID_244156,Human_RBP_ID_778535,Human_RBP_ID_1599817,Human_RBP_ID_1932156,Human_RBP_ID_2691857,Human_RBP_ID_3652321,Human_RBP_ID_4654729,Human_RBP_ID_5595243,Human_RBP_ID_8856569,Human_RBP_ID_14155476,Human_RBP_ID_17974929,Human_RBP_ID_18193796,Human_RBP_ID_19106864,Human_RBP_ID_23913578,Human_RBP_ID_25628005 Human_Splice_Rec_2098138,Human_Splice_Rec_2098139,Human_Splice_Rec_2098167,Human_Splice_Rec_2098192,Human_Splice_Rec_2098193,Human_Splice_Rec_2098216,Human_Splice_Rec_2098217,Human_Splice_Rec_2098240,Human_Splice_Rec_2098241,Human_Splice_Rec_2098254,Human_Splice_Rec_2098255,Human_Splice_Rec_2098265,Human_Splice_Rec_2098270,Human_Splice_Rec_2098271,Human_Splice_Rec_2098283,Human_Splice_Rec_2098302,Human_Splice_Rec_2098303,Human_Splice_Rec_2098313,Human_Splice_Rec_2098326,Human_Splice_Rec_2098327,Human_Splice_Rec_2098349,Human_Splice_Rec_2098374,Human_Splice_Rec_2098375,Human_Splice_Rec_2098406,Human_Splice_Rec_2098407,Human_Splice_Rec_2098417,Human_Splice_Rec_2098435,Human_Splice_Rec_2098454,Human_Splice_Rec_2098455,Human_Splice_Rec_2098469,Human_Splice_Rec_2098484,Human_Splice_Rec_2098485,Human_Splice_Rec_2098500,Human_Splice_Rec_2098501,Human_Splice_Rec_2098521,Human_Splice_Rec_2098529,Human_Splice_Rec_2098546,Human_Splice_Rec_2098547,Human_Splice_Rec_2098558,Human_Splice_Rec_2098559,Human_Splice_Rec_2098567,Human_Splice_Rec_2098576,Human_Splice_Rec_2098577,Human_Splice_Rec_2098588,Human_Splice_Rec_2098589,Human_Splice_Rec_2098613,Human_Splice_Rec_2098635,Human_Splice_Rec_2098658,Human_Splice_Rec_2098659,Human_Splice_Rec_2098681,Human_Splice_Rec_2098702,Human_Splice_Rec_2098703,Human_Splice_Rec_2098742,Human_Splice_Rec_2098743,Human_Splice_Rec_2098760,Human_Splice_Rec_2098761,Human_Splice_Rec_2098775,Human_Splice_Rec_2098792,Human_Splice_Rec_2098793,Human_Splice_Rec_2098802,Human_Splice_Rec_2098803,Human_Splice_Rec_2098822,Human_Splice_Rec_2098823,Human_Splice_Rec_2098841,Human_Splice_Rec_2098859,Human_Splice_Rec_2098869 RMVar_hsa_circ_14526,RMVar_hsa_circ_278184,RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_70998,RMVar_hsa_circ_344347,RMVar_hsa_circ_211085,RMVar_hsa_circ_211086,RMVar_hsa_circ_374022,RMVar_hsa_circ_211088,RMVar_hsa_circ_211087,RMVar_hsa_circ_374296 67954 RMVar_ID_67954 Human_SNP_ID_685737800 m1A Human chr20 + 58903561 58903561 58903561 AGTGAGAAGGCAACCAAAGTGCAGGACATCAAAAACAACCTGAAAGAGGCGATTGAAGTACGTGC AGTGAGAAGGCAACCAAAGTGCAGGACATCAAGAACAACCTGAAAGAGGCGATTGAAGTACGTGC A G GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:58903526..58903600 26863196 MeRIP-seq:(Medium) rs755397365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62047,Human_RBP_ID_1599817,Human_RBP_ID_1932156,Human_RBP_ID_2691857,Human_RBP_ID_3652321,Human_RBP_ID_4654729,Human_RBP_ID_5595243,Human_RBP_ID_8856569,Human_RBP_ID_14155476,Human_RBP_ID_17974929,Human_RBP_ID_18193796,Human_RBP_ID_19106864,Human_RBP_ID_23913579,Human_RBP_ID_25628005 Human_Splice_Rec_2098138,Human_Splice_Rec_2098139,Human_Splice_Rec_2098167,Human_Splice_Rec_2098192,Human_Splice_Rec_2098193,Human_Splice_Rec_2098216,Human_Splice_Rec_2098217,Human_Splice_Rec_2098240,Human_Splice_Rec_2098241,Human_Splice_Rec_2098254,Human_Splice_Rec_2098255,Human_Splice_Rec_2098265,Human_Splice_Rec_2098270,Human_Splice_Rec_2098271,Human_Splice_Rec_2098283,Human_Splice_Rec_2098302,Human_Splice_Rec_2098303,Human_Splice_Rec_2098313,Human_Splice_Rec_2098326,Human_Splice_Rec_2098327,Human_Splice_Rec_2098349,Human_Splice_Rec_2098374,Human_Splice_Rec_2098375,Human_Splice_Rec_2098406,Human_Splice_Rec_2098407,Human_Splice_Rec_2098417,Human_Splice_Rec_2098435,Human_Splice_Rec_2098454,Human_Splice_Rec_2098455,Human_Splice_Rec_2098469,Human_Splice_Rec_2098484,Human_Splice_Rec_2098485,Human_Splice_Rec_2098500,Human_Splice_Rec_2098501,Human_Splice_Rec_2098521,Human_Splice_Rec_2098529,Human_Splice_Rec_2098546,Human_Splice_Rec_2098547,Human_Splice_Rec_2098558,Human_Splice_Rec_2098559,Human_Splice_Rec_2098567,Human_Splice_Rec_2098576,Human_Splice_Rec_2098577,Human_Splice_Rec_2098588,Human_Splice_Rec_2098589,Human_Splice_Rec_2098613,Human_Splice_Rec_2098635,Human_Splice_Rec_2098658,Human_Splice_Rec_2098659,Human_Splice_Rec_2098681,Human_Splice_Rec_2098702,Human_Splice_Rec_2098703,Human_Splice_Rec_2098742,Human_Splice_Rec_2098743,Human_Splice_Rec_2098760,Human_Splice_Rec_2098761,Human_Splice_Rec_2098775,Human_Splice_Rec_2098792,Human_Splice_Rec_2098793,Human_Splice_Rec_2098802,Human_Splice_Rec_2098803,Human_Splice_Rec_2098822,Human_Splice_Rec_2098823,Human_Splice_Rec_2098841,Human_Splice_Rec_2098859,Human_Splice_Rec_2098869 Human_miRNA_ID_184369 RMVar_hsa_circ_14526,RMVar_hsa_circ_278184,RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_70998,RMVar_hsa_circ_344347,RMVar_hsa_circ_211085,RMVar_hsa_circ_211086,RMVar_hsa_circ_374022,RMVar_hsa_circ_211088,RMVar_hsa_circ_211087,RMVar_hsa_circ_374296 67955 RMVar_ID_67955 Human_SNP_ID_685737810 m1A Human chr20 - 58903587 58903587 58903587 TACAAGACAGACAGCACAAGGAGCCAGCACGTACTTCAATCGCCTCTTTCAGGTTGTTTTTGATG TACAAGACAGACAGCACAAGGAGCCAGCACGTGCTTCAATCGCCTCTTTCAGGTTGTTTTTGATG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58903526..58905500 32194978 MeRIP-seq:(Medium) rs112364266 Functional Loss SNV dbSNP153 33..33 33 - - - 67956 RMVar_ID_67956 Human_SNP_ID_685739773 m1A Human chr20 + 58910788 58910786 58910789 ACATCCGCCGTGTGTTCAACGACTGCCGTGACATCATTCAGCGCATGCACCTTCGTCAGTACGAG ACATCCGCCGTGTGTTCAACGACTGCCGTGA___CATTCAGCGCATGCACCTTCGTCAGTACGAG ACAT A GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1569032751 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_62066,Human_RBP_ID_281610,Human_RBP_ID_567492,Human_RBP_ID_1026993,Human_RBP_ID_1599849,Human_RBP_ID_1932173,Human_RBP_ID_4665334,Human_RBP_ID_8537207,Human_RBP_ID_8856584,Human_RBP_ID_17282414,Human_RBP_ID_17512490,Human_RBP_ID_17974938,Human_RBP_ID_18209354,Human_RBP_ID_18444639,Human_RBP_ID_18776071,Human_RBP_ID_22395387,Human_RBP_ID_26492134,Human_RBP_ID_27023417 Human_miRNA_ID_2144182,Human_miRNA_ID_2145711 Clinvar_Rec_274 RMVar_hsa_circ_2212,RMVar_hsa_circ_118782,RMVar_hsa_circ_211090 67957 RMVar_ID_67957 Human_SNP_ID_685739773 m1A Human chr20 - 58910789 58910786 58910789 GCTCGTACTGACGAAGGTGCATGCGCTGAATGATGTCACGGCAGTCGTTGAACACACGGCGGATG GCTCGTACTGACGAAGGTGCATGCGCTGAATG___TCACGGCAGTCGTTGAACACACGGCGGATG ACAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58910738..58911131 26863196 MeRIP-seq:(Medium) rs1569032751 Functional Loss DEL dbSNP153 33..35 33 - - - Clinvar_Rec_274 67958 RMVar_ID_67958 Human_SNP_ID_685739792 m1A Human chr20 + 58910854 58910854 58910854 TGCTCTAAGAAGGGAACCCCCAAATTTAATTAAAGCCTTAAGCACAATTAATTAAAAGTGAAACG TGCTCTAAGAAGGGAACCCCCAAATTTAATTAGAGCCTTAAGCACAATTAATTAAAAGTGAAACG A G GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:58910752..58911043 26863410 MeRIP-seq:(Medium) rs746559018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62067,Human_RBP_ID_244166,Human_RBP_ID_567495,Human_RBP_ID_1026994,Human_RBP_ID_1932176,Human_RBP_ID_2691883,Human_RBP_ID_3652339,Human_RBP_ID_4654763,Human_RBP_ID_7017235,Human_RBP_ID_17700856,Human_RBP_ID_18324020,Human_RBP_ID_18776073,Human_RBP_ID_22395388,Human_RBP_ID_22817906,Human_RBP_ID_23006074,Human_RBP_ID_23913603,Human_RBP_ID_25622989,Human_RBP_ID_26671951,Human_RBP_ID_27023419,Human_RBP_ID_27298955 Human_miRNA_ID_2237869 RMVar_hsa_circ_118782,RMVar_hsa_circ_211090 67959 RMVar_ID_67959 Human_SNP_ID_685757225 m1A Human chr20 - 58981325 58981324 58981325 AGCCTCGTCGCCCCACTCGGCCGCGCTCCCGTAGTAGTCCTCGTCCATGATGGCGCCCGGCACGG AGCCTCGTCGCCCCACTCGGCCGCGCTCCCGT_GTAGTCCTCGTCCATGATGGCGCCCGGCACGG CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58981251..58986200 26863196 MeRIP-seq:(Medium) rs1156956957 Functional Loss DEL dbSNP153 33..33 33 - - - 67960 RMVar_ID_67960 Human_SNP_ID_685757230 m1A Human chr20 + 58981331 58981331 58981331 CGGGCGCCATCATGGACGAGGACTACTACGGGAGCGCGGCCGAGTGGGGCGACGAGGCTGACGGC CGGGCGCCATCATGGACGAGGACTACTACGGGGGCGCGGCCGAGTGGGGCGACGAGGCTGACGGC A G NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58981251..58986225 26863196 MeRIP-seq:(Medium) rs1158356321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779725,Human_RBP_ID_4659944,Human_RBP_ID_9391045,Human_RBP_ID_26343804,Human_RBP_ID_27820448 Human_Splice_Rec_2098935,Human_Splice_Rec_2098963,Human_Splice_Rec_2098967,Human_Splice_Rec_2098973,Human_Splice_Rec_2099001,Human_Splice_Rec_2099003,Human_Splice_Rec_2099013 67961 RMVar_ID_67961 Human_SNP_ID_685758774 m1A Human chr20 - 58986784 58986784 58986784 GCGGTGTAGTTTTCAGATAAGAGCTGGATAACATTCTCTGGAGACCCTCCTGCCTGAAAATACCT GCGGTGTAGTTTTCAGATAAGAGCTGGATAACGTTCTCTGGAGACCCTCCTGCCTGAAAATACCT T C lnc-CTSZ-6 RNACentral:URS00008BDF7C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58986751..58986825 26863196 MeRIP-seq:(Medium) rs753028723 Functional Loss SNV dbSNP153 33..33 33 - - - 67962 RMVar_ID_67962 Human_SNP_ID_685759619 m1A Human chr20 - 58989955 58989955 58989955 TCTCCTGGGCAAAGCGCTGCACTTCCTGGGCGATCCTGCGCACAGCGGAGCCCCCCTGCTCCTCC TCTCCTGGGCAAAGCGCTGCACTTCCTGGGCGTTCCTGCGCACAGCGGAGCCCCCCTGCTCCTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58989909..58990031 26863196 MeRIP-seq:(Medium) rs1023567196 Functional Loss SNV dbSNP153 33..33 33 - - - 67963 RMVar_ID_67963 Human_SNP_ID_685759906 m1A Human chr20 + 58990975 58990970 58990976 GGGCACAGCTGCCTCCTACCCCAGGGCCTGCCAGGCTCTCGGGGCCATGCTGTCCAAAGGAGCCC GGGCACAGCTGCCTCCTACCCCAGGGCC______GCTCTCGGGGCCATGCTGTCCAAAGGAGCCC CTGCCAG C NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58990901..58990975 32194978 MeRIP-seq:(Medium) rs1287865274 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_832373 Human_Splice_Rec_2098948,Human_Splice_Rec_2098986,Human_Splice_Rec_2099026,Human_Splice_Rec_2099050,Human_Splice_Rec_2099070 RMVar_hsa_circ_12452,RMVar_hsa_circ_16165,RMVar_hsa_circ_27596,RMVar_hsa_circ_45609,RMVar_hsa_circ_211091,RMVar_hsa_circ_62354,RMVar_hsa_circ_120395,RMVar_hsa_circ_211095,RMVar_hsa_circ_115143,RMVar_hsa_circ_211094 67964 RMVar_ID_67964 Human_SNP_ID_685759922 m1A Human chr20 - 58991032 58991032 58991032 GAGGAGGGTCCATGCTTGTGAACATCTTGAACAGGACGGTGATGTCAGCAGGGTTCAGGGCTCCT GAGGAGGGTCCATGCTTGTGAACATCTTGAACGGGACGGTGATGTCAGCAGGGTTCAGGGCTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58990981..58991087 26863196 MeRIP-seq:(Medium) rs1447069714 Functional Loss SNV dbSNP153 33..33 33 - - - 67965 RMVar_ID_67965 Human_SNP_ID_685760045 m1A Human chr20 + 58991423 58991423 58991423 ACAAATACATCCACATCTTGGCGTACGCAGCAAGCGTGGTTGAGACCTGGAAGAAGGTACCATCG ACAAATACATCCACATCTTGGCGTACGCAGCAGGCGTGGTTGAGACCTGGAAGAAGGTACCATCG A G NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58991375..58991476 32194978 MeRIP-seq:(Medium) rs771039440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778661,Human_RBP_ID_832357,Human_RBP_ID_1932199,Human_RBP_ID_3960952,Human_RBP_ID_5595249,Human_RBP_ID_9391053,Human_RBP_ID_14155842 Human_Splice_Rec_2098951,Human_Splice_Rec_2098989,Human_Splice_Rec_2099029,Human_Splice_Rec_2099053,Human_Splice_Rec_2099073,Human_Splice_Rec_2099091,Human_Splice_Rec_2099099 RMVar_hsa_circ_12452,RMVar_hsa_circ_27596,RMVar_hsa_circ_45609,RMVar_hsa_circ_211091,RMVar_hsa_circ_120395,RMVar_hsa_circ_211095,RMVar_hsa_circ_115143,RMVar_hsa_circ_211094,RMVar_hsa_circ_211096,RMVar_hsa_circ_88791 67966 RMVar_ID_67966 Human_SNP_ID_685760551 m1A Human chr20 - 58993508 58993508 58993508 TCCATCACGTCCAGCTGGGAGTGCTCAGTCTCAAAAAGCTTAACAAGCAGCTGCAGGACCTGGGG TCCATCACGTCCAGCTGGGAGTGCTCAGTCTCGAAAAGCTTAACAAGCAGCTGCAGGACCTGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58993451..58993525 32194978 MeRIP-seq:(Medium) rs144257648 Functional Loss SNV dbSNP153 33..33 33 - - - 67967 RMVar_ID_67967 Human_SNP_ID_685760552 m1A Human chr20 - 58993508 58993508 58993508 TCCATCACGTCCAGCTGGGAGTGCTCAGTCTCAAAAAGCTTAACAAGCAGCTGCAGGACCTGGGG TCCATCACGTCCAGCTGGGAGTGCTCAGTCTCCAAAAGCTTAACAAGCAGCTGCAGGACCTGGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:58993451..58993525 32194978 MeRIP-seq:(Medium) rs144257648 Functional Loss SNV dbSNP153 33..33 33 - - - 67968 RMVar_ID_67968 Human_SNP_ID_685760632 m1A Human chr20 + 58993759 58993759 58993759 ACACTGACATTTCACTCATTCGCTATTTTGTCACTGAGGTCAGCAATGCACCGTTGGTTTCATGT ACACTGACATTTCACTCATTCGCTATTTTGTCGCTGAGGTCAGCAATGCACCGTTGGTTTCATGT A G NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58993631..58993781 32194978 MeRIP-seq:(Medium) rs1485933900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119197,Human_RBP_ID_5382730,Human_RBP_ID_14155862,Human_RBP_ID_17512494,Human_RBP_ID_18168092,Human_RBP_ID_19109638,Human_RBP_ID_22081435,Human_RBP_ID_23003990,Human_RBP_ID_24424858,Human_RBP_ID_25623089 Human_Splice_Rec_2098959,Human_Splice_Rec_2098997,Human_Splice_Rec_2099037 RMVar_hsa_circ_12452,RMVar_hsa_circ_211091,RMVar_hsa_circ_211095,RMVar_hsa_circ_115143,RMVar_hsa_circ_18322,RMVar_hsa_circ_288121 67969 RMVar_ID_67969 Human_SNP_ID_685761074 m1A Human chr20 + 58995033 58995033 58995033 GAACTCCTTTCCAAGCTGACCTCAGTTTTCTCACAAGAACCCAGTTAGCTGATGTTTTATTGTAA GAACTCCTTTCCAAGCTGACCTCAGTTTTCTCCCAAGAACCCAGTTAGCTGATGTTTTATTGTAA A C NELFCD Ensembl:ENSG00000101158 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58994982..58995083 32194978 MeRIP-seq:(Medium) rs375356368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_567543,Human_RBP_ID_1599892,Human_RBP_ID_1932217,Human_RBP_ID_2691934,Human_RBP_ID_8537247,Human_RBP_ID_17282434,Human_RBP_ID_18444649,Human_RBP_ID_18776112,Human_RBP_ID_25623110 Human_miRNA_ID_1794258 RMVar_hsa_circ_107143,RMVar_hsa_circ_211099 67970 RMVar_ID_67970 Human_SNP_ID_685761075 m1A Human chr20 + 58995033 58995033 58995033 GAACTCCTTTCCAAGCTGACCTCAGTTTTCTCACAAGAACCCAGTTAGCTGATGTTTTATTGTAA GAACTCCTTTCCAAGCTGACCTCAGTTTTCTCTCAAGAACCCAGTTAGCTGATGTTTTATTGTAA A T NELFCD Ensembl:ENSG00000101158 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58994982..58995083 32194978 MeRIP-seq:(Medium) rs375356368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_567543,Human_RBP_ID_1599892,Human_RBP_ID_1932217,Human_RBP_ID_2691934,Human_RBP_ID_8537247,Human_RBP_ID_17282434,Human_RBP_ID_18444649,Human_RBP_ID_18776112,Human_RBP_ID_25623110 Human_miRNA_ID_1794258 RMVar_hsa_circ_107143,RMVar_hsa_circ_211099 67971 RMVar_ID_67971 Human_SNP_ID_685761292 m1A Human chr20 - 58995755 58995755 58995755 GGCTGACGCGCGATCCCACTTCTCACAGGGCGAGAGAGGCTGGCTGAGGATCGTGACCAGCACCT GGCTGACGCGCGATCCCACTTCTCACAGGGCGGGAGAGGCTGGCTGAGGATCGTGACCAGCACCT T C CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58995333..58995830 26863196 MeRIP-seq:(Medium) rs994175727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119202,Human_RBP_ID_22767061 Human_Splice_Rec_2099124 67972 RMVar_ID_67972 Human_SNP_ID_685761293 m1A Human chr20 - 58995755 58995755 58995755 GGCTGACGCGCGATCCCACTTCTCACAGGGCGAGAGAGGCTGGCTGAGGATCGTGACCAGCACCT GGCTGACGCGCGATCCCACTTCTCACAGGGCGCGAGAGGCTGGCTGAGGATCGTGACCAGCACCT T G CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58995333..58995830 26863196 MeRIP-seq:(Medium) rs994175727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119202,Human_RBP_ID_22767061 Human_Splice_Rec_2099124 67973 RMVar_ID_67973 Human_SNP_ID_685761570 m1A Human chr20 + 58996628 58996628 58996628 GTTTTTTTCTAGGAATGACCTTAAGAAAATGAAAACATCTTACCCATGGTTCACCCCATGAATTC GTTTTTTTCTAGGAATGACCTTAAGAAAATGAGAACATCTTACCCATGGTTCACCCCATGAATTC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:58996626..58996675 26863196 MeRIP-seq:(Medium) rs773614700 Functional Loss SNV dbSNP153 33..33 33 - - - 67974 RMVar_ID_67974 Human_SNP_ID_685761637 m1A Human chr20 + 58996790 58996790 58996790 CTCCGGTGTAGTTAGCCAGTCTTTCTGTTGCCATTATTCCACAGCTGAGAGCAAGCAGTTAAAGA CTCCGGTGTAGTTAGCCAGTCTTTCTGTTGCCGTTATTCCACAGCTGAGAGCAAGCAGTTAAAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr20:58996726..58996825;chr20:58995326..58996825 32194978 MeRIP-seq:(Medium) rs141912408 Functional Loss SNV dbSNP153 33..33 33 - - - 67975 RMVar_ID_67975 Human_SNP_ID_685762020 m1A Human chr20 + 58997740 58997740 58997740 TCTTTGAATTCATTGCATGTCCCACATTGGTTAAACTTGTCACACTCTGGGGGAGAGCAAGAAAA TCTTTGAATTCATTGCATGTCCCACATTGGTTTAACTTGTCACACTCTGGGGGAGAGCAAGAAAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58997490..58997799 26863196 MeRIP-seq:(Medium) rs1018121290 Functional Loss SNV dbSNP153 33..33 33 - - - 67976 RMVar_ID_67976 Human_SNP_ID_685762023 m1A Human chr20 - 58997753 58997751 58997753 GCCTCATGCTGACTTTTCTTGCTCTCCCCCAGAGTGTGACAAGTTTAACCAATGTGGGACATGCA GCCTCATGCTGACTTTTCTTGCTCTCCCCCAG__TGTGACAAGTTTAACCAATGTGGGACATGCA ACT A CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58997751..58997775 26863196 MeRIP-seq:(Medium) rs758455489 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_21983362,Human_RBP_ID_22671056,Human_RBP_ID_22743838,Human_RBP_ID_25623116 Human_Splice_Rec_2099120,Human_Splice_Rec_2099130,Human_Splice_Rec_2099136 RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 67977 RMVar_ID_67977 Human_SNP_ID_685762024 m1A Human chr20 - 58997753 58997753 58997753 GCCTCATGCTGACTTTTCTTGCTCTCCCCCAGAGTGTGACAAGTTTAACCAATGTGGGACATGCA GCCTCATGCTGACTTTTCTTGCTCTCCCCCAGTGTGTGACAAGTTTAACCAATGTGGGACATGCA T A CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:58997751..58997775 26863196 MeRIP-seq:(Medium) rs750885462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21983362,Human_RBP_ID_22671056,Human_RBP_ID_22743838,Human_RBP_ID_25623116 Human_Splice_Rec_2099120,Human_Splice_Rec_2099130,Human_Splice_Rec_2099136 RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 67978 RMVar_ID_67978 Human_SNP_ID_685763209 m1A Human chr20 + 59001643 59001643 59001643 GGCCACGCTCCCTTCCTCTTGATGTTGATCCGATCTGCAACAGTCAGCACCTGCCAGTCAGCACT GGCCACGCTCCCTTCCTCTTGATGTTGATCCGTTCTGCAACAGTCAGCACCTGCCAGTCAGCACT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:59001417..59001712 26863196 MeRIP-seq:(Medium) rs1568683209 Functional Loss SNV dbSNP153 33..33 33 - - - 67979 RMVar_ID_67979 Human_SNP_ID_685764012 m1A Human chr20 - 59004875 59004875 59004875 TTCAGATGGATGTGGGACCCTGGCCAGGGGTCAGCCCTGCCGCATTTCCCCAGGGGACTCTCTCT TTCAGATGGATGTGGGACCCTGGCCAGGGGTCGGCCCTGCCGCATTTCCCCAGGGGACTCTCTCT T C CTSZ Ensembl:ENSG00000101160 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:59004871..59005157 26863196 MeRIP-seq:(Medium) rs897838209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57119,RMVar_hsa_circ_302597,RMVar_hsa_circ_211101,RMVar_hsa_circ_211102,RMVar_hsa_circ_372909 67980 RMVar_ID_67980 Human_SNP_ID_685764375 m1A Human chr20 - 59006381 59006381 59006381 TGGTGTCAACTATGCCAGCATCACCCGGAACCAGCACATCCCCCAATACTGCGGCTCCTGCTGGG TGGTGTCAACTATGCCAGCATCACCCGGAACCGGCACATCCCCCAATACTGCGGCTCCTGCTGGG T C CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr20:59006285..59006516;chr20:59006301..59007075 26863196,32194978 MeRIP-seq:(Medium) rs748470022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18209356,Human_RBP_ID_22767066,Human_RBP_ID_27487665 Human_Splice_Rec_2099117,Human_Splice_Rec_2099127,Human_Splice_Rec_2099133 Human_miRNA_ID_272941,Human_miRNA_ID_1322162,Human_miRNA_ID_2653749,Human_miRNA_ID_2754947 RMVar_hsa_circ_57119,RMVar_hsa_circ_302597,RMVar_hsa_circ_211101,RMVar_hsa_circ_81573,RMVar_hsa_circ_211102,RMVar_hsa_circ_372909,RMVar_hsa_circ_211103 67981 RMVar_ID_67981 Human_SNP_ID_685769132 m1A Human chr20 - 59024237 59024237 59024237 TACTGCTGGCTGCCCTGGGCCGTGAGTGGGGCAAAGCCGGGCATAAAGAAGTGCAGGCGGGGGAA TACTGCTGGCTGCCCTGGGCCGTGAGTGGGGCTAAGCCGGGCATAAAGAAGTGCAGGCGGGGGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59024199..59024368 26863196 MeRIP-seq:(Medium) rs1389479127 Functional Loss SNV dbSNP153 33..33 33 - - - 67982 RMVar_ID_67982 Human_SNP_ID_685769144 m1A Human chr20 - 59024278 59024278 59024278 CGAACATCTGCTGGGTGAGCTCGGCCACGGAGAGGGCTCGGTACTGCTGGCTGCCCTGGGCCGTG CGAACATCTGCTGGGTGAGCTCGGCCACGGAGGGGGCTCGGTACTGCTGGCTGCCCTGGGCCGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:59024234..59024337 26863196 MeRIP-seq:(Medium) rs1486480239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14155974 67983 RMVar_ID_67983 Human_SNP_ID_685771313 m1A Human chr20 - 59032274 59032274 59032274 CGACATTGCCGGCGTCTTGGCGATTCGGCCCGACGAGCTCCGCTTTCGCTACAGCATGGTGGCCT CGACATTGCCGGCGTCTTGGCGATTCGGCCCGTCGAGCTCCGCTTTCGCTACAGCATGGTGGCCT T A ATP5F1E Ensembl:ENSG00000124172 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr20:59032207..59032350;chr20:59032207..59032290;chr20:59032201..59032325 26863196,32194978 MeRIP-seq:(Medium) rs771243724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244348,Human_RBP_ID_567597,Human_RBP_ID_778855,Human_RBP_ID_1027015,Human_RBP_ID_1599908,Human_RBP_ID_4654893,Human_RBP_ID_5322987,Human_RBP_ID_5423982,Human_RBP_ID_5445819,Human_RBP_ID_5472275,Human_RBP_ID_5503619,Human_RBP_ID_8537279,Human_RBP_ID_9331615,Human_RBP_ID_17396662,Human_RBP_ID_17512503,Human_RBP_ID_17658823,Human_RBP_ID_22452814,Human_RBP_ID_22531644,Human_RBP_ID_24533928,Human_RBP_ID_27487674,Human_RBP_ID_27564763 Human_Splice_Rec_2099145,Human_Splice_Rec_2099149,Human_Splice_Rec_2099153 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104 67984 RMVar_ID_67984 Human_SNP_ID_685771314 m1A Human chr20 - 59032274 59032274 59032274 CGACATTGCCGGCGTCTTGGCGATTCGGCCCGACGAGCTCCGCTTTCGCTACAGCATGGTGGCCT CGACATTGCCGGCGTCTTGGCGATTCGGCCCGGCGAGCTCCGCTTTCGCTACAGCATGGTGGCCT T C ATP5F1E Ensembl:ENSG00000124172 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr20:59032207..59032350;chr20:59032207..59032290;chr20:59032201..59032325 26863196,32194978 MeRIP-seq:(Medium) rs771243724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244348,Human_RBP_ID_567597,Human_RBP_ID_778855,Human_RBP_ID_1027015,Human_RBP_ID_1599908,Human_RBP_ID_4654893,Human_RBP_ID_5322987,Human_RBP_ID_5423982,Human_RBP_ID_5445819,Human_RBP_ID_5472275,Human_RBP_ID_5503619,Human_RBP_ID_8537279,Human_RBP_ID_9331615,Human_RBP_ID_17396662,Human_RBP_ID_17512503,Human_RBP_ID_17658823,Human_RBP_ID_22452814,Human_RBP_ID_22531644,Human_RBP_ID_24533928,Human_RBP_ID_27487674,Human_RBP_ID_27564763 Human_Splice_Rec_2099145,Human_Splice_Rec_2099149,Human_Splice_Rec_2099153 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104 67985 RMVar_ID_67985 Human_SNP_ID_685771335 m1A Human chr20 + 59032289 59032289 59032289 AGCGAAAGCGGAGCTCGTCGGGCCGAATCGCCAAGACGCCGGCAATGTCGGCTCAGCCGGGCGGT AGCGAAAGCGGAGCTCGTCGGGCCGAATCGCCCAGACGCCGGCAATGTCGGCTCAGCCGGGCGGT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr20:59032160..59032350;chr20:59032226..59032300 26863196 MeRIP-seq:(Medium) rs1378332870 Functional Loss SNV dbSNP153 33..33 33 - - - 67986 RMVar_ID_67986 Human_SNP_ID_685771339 m1A Human chr20 + 59032292 59032292 59032292 GAAAGCGGAGCTCGTCGGGCCGAATCGCCAAGACGCCGGCAATGTCGGCTCAGCCGGGCGGTTCA GAAAGCGGAGCTCGTCGGGCCGAATCGCCAAGCCGCCGGCAATGTCGGCTCAGCCGGGCGGTTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59032243..59032350 26863196 MeRIP-seq:(Medium) rs759139093 Functional Loss SNV dbSNP153 33..33 33 - - - 67987 RMVar_ID_67987 Human_SNP_ID_685771340 m1A Human chr20 + 59032292 59032292 59032292 GAAAGCGGAGCTCGTCGGGCCGAATCGCCAAGACGCCGGCAATGTCGGCTCAGCCGGGCGGTTCA GAAAGCGGAGCTCGTCGGGCCGAATCGCCAAGTCGCCGGCAATGTCGGCTCAGCCGGGCGGTTCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59032243..59032350 26863196 MeRIP-seq:(Medium) rs759139093 Functional Loss SNV dbSNP153 33..33 33 - - - 67988 RMVar_ID_67988 Human_SNP_ID_685771357 m1A Human chr20 - 59032304 59032304 59032304 TCTTCCTGCGGCTGAACCGCCCGGCTGAGCCGACATTGCCGGCGTCTTGGCGATTCGGCCCGACG TCTTCCTGCGGCTGAACCGCCCGGCTGAGCCGGCATTGCCGGCGTCTTGGCGATTCGGCCCGACG T C ATP5F1E Ensembl:ENSG00000124172 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:59032301..59032350 32194978 MeRIP-seq:(Medium) rs1186288495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244348,Human_RBP_ID_567598,Human_RBP_ID_778856,Human_RBP_ID_4659502,Human_RBP_ID_5322987,Human_RBP_ID_5472276,Human_RBP_ID_9331615,Human_RBP_ID_17396662,Human_RBP_ID_17658823,Human_RBP_ID_22452814,Human_RBP_ID_22531644,Human_RBP_ID_24533928,Human_RBP_ID_27023462,Human_RBP_ID_27298985 Human_Splice_Rec_2099145,Human_Splice_Rec_2099149,Human_Splice_Rec_2099153 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104 67989 RMVar_ID_67989 Human_SNP_ID_685771394 m1A Human chr20 + 59032349 59032349 59032349 GCGGTTCAGCCGCAGGAAGATCAGACCACAGAAGCGGAAGAGGCGGGGCGTGCGGACCTGCCAAT GCGGTTCAGCCGCAGGAAGATCAGACCACAGAGGCGGAAGAGGCGGGGCGTGCGGACCTGCCAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:59032326..59032350 26863196 MeRIP-seq:(Medium) rs544647396 Functional Loss SNV dbSNP153 33..33 33 - - - 67990 RMVar_ID_67990 Human_SNP_ID_685772026 m1A Human chr20 - 59034911 59034911 59034911 TGTTATTTTAAAAATACAACTATATTTTGGGTAGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG TGTTATTTTAAAAATACAACTATATTTTGGGTTGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG T A PRELID3B Ensembl:ENSG00000101166 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs894717498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_567667,Human_RBP_ID_1027035,Human_RBP_ID_7017436,Human_RBP_ID_9118659,Human_RBP_ID_17396299,Human_RBP_ID_17975005,Human_RBP_ID_23284184,Human_RBP_ID_27703703 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104,RMVar_hsa_circ_211106,RMVar_hsa_circ_90966 67991 RMVar_ID_67991 Human_SNP_ID_685772027 m1A Human chr20 - 59034911 59034911 59034911 TGTTATTTTAAAAATACAACTATATTTTGGGTAGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG TGTTATTTTAAAAATACAACTATATTTTGGGTGGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG T C PRELID3B Ensembl:ENSG00000101166 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs894717498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_567667,Human_RBP_ID_1027035,Human_RBP_ID_7017436,Human_RBP_ID_9118659,Human_RBP_ID_17396299,Human_RBP_ID_17975005,Human_RBP_ID_23284184,Human_RBP_ID_27703703 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104,RMVar_hsa_circ_211106,RMVar_hsa_circ_90966 67992 RMVar_ID_67992 Human_SNP_ID_685772527 m1A Human chr20 - 59036762 59036762 59036762 GATTTGATCTTTTTTTTTTTTCTTCATTCTGTAGATTTCATTTACAAACATGGTTTCAGTAGATG GATTTGATCTTTTTTTTTTTTCTTCATTCTGTGGATTTCATTTACAAACATGGTTTCAGTAGATG T C PRELID3B Ensembl:ENSG00000101166 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:59034334..59037217 32194978 MeRIP-seq:(Medium) rs13045843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25623145 Human_Splice_Rec_2099161,Human_Splice_Rec_2099169,Human_Splice_Rec_2099179 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211104,RMVar_hsa_circ_211106,RMVar_hsa_circ_90966,RMVar_hsa_circ_332153,RMVar_hsa_circ_126090,RMVar_hsa_circ_54002,RMVar_hsa_circ_211108 67993 RMVar_ID_67993 Human_SNP_ID_685773917 m1A Human chr20 - 59042591 59042591 59042591 CCGCAGGAGGCTTCTAGGCGTCGGGCCTAGCGAGGGGAGCGAACTCTGAAGCCTGCGGGCCCCGG CCGCAGGAGGCTTCTAGGCGTCGGGCCTAGCGGGGGGAGCGAACTCTGAAGCCTGCGGGCCCCGG T C PRELID3B Ensembl:ENSG00000101166 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59042589..59042682 26863196 MeRIP-seq:(Medium) rs1169432566 Functional Loss SNV dbSNP153 33..33 33 - - - 67994 RMVar_ID_67994 Human_SNP_ID_685809394 m1A Human chr20 - 59192344 59192344 59192344 GGAAGGAGTCCTTGTAGGTGTAGGGCGTGGGCAGGTCGATGCTGCCCTGTTTGGACAGCCCGGTC GGAAGGAGTCCTTGTAGGTGTAGGGCGTGGGCTGGTCGATGCTGCCCTGTTTGGACAGCCCGGTC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:59192297..59192550 26863196 MeRIP-seq:(Medium) rs1319017260 Functional Loss SNV dbSNP153 33..33 33 - - - 67995 RMVar_ID_67995 Human_SNP_ID_685809453 m1A Human chr20 + 59192442 59192442 59192442 GGAGGGCCCCGGGCCCCGTGCGCTCCACCTGGACGCCCCCAGACAAGTCTCGGCCCCTCTTCTTC GGAGGGCCCCGGGCCCCGTGCGCTCCACCTGGGCGCCCCCAGACAAGTCTCGGCCCCTCTTCTTC A G ZNF831 Ensembl:ENSG00000124203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:59192283..59192525 26863196 MeRIP-seq:(Medium) rs575127906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27487706 RMVar_hsa_circ_64755 67996 RMVar_ID_67996 Human_SNP_ID_685809627 m1A Human chr20 - 59192860 59192860 59192860 CCCCGTACACCTGCCACTTCTCCTGGGAGAACATCTTCAGCCTTCTCTGGCCGCACTTCCTGCCG CCCCGTACACCTGCCACTTCTCCTGGGAGAACTTCTTCAGCCTTCTCTGGCCGCACTTCCTGCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59192780..59192946 26863196 MeRIP-seq:(Medium) rs1244980030 Functional Loss SNV dbSNP153 33..33 33 - - - 67997 RMVar_ID_67997 Human_SNP_ID_685809754 m1A Human chr20 + 59193168 59193168 59193168 AACCCACTAAGCATGGGGAGACGGTGGCCAGGAGAGGAGACAGTGACCGACCCAGGGTGGAAGAG AACCCACTAAGCATGGGGAGACGGTGGCCAGGTGAGGAGACAGTGACCGACCCAGGGTGGAAGAG A T ZNF831 Ensembl:ENSG00000124203 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59193118..59193217 26863196 MeRIP-seq:(Medium) rs756613604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64755 67998 RMVar_ID_67998 Human_SNP_ID_685824477 m1A Human chr20 - 59254220 59254220 59254220 CTCGTGATTCAGCACTGTGAATTTCCTGGGCTATGTGATCTGTTCTCACTGGCAGAGAAATACAA CTCGTGATTCAGCACTGTGAATTTCCTGGGCTGTGTGATCTGTTCTCACTGGCAGAGAAATACAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:59254169..59254265 26863196 MeRIP-seq:(Medium) rs1479242786 Functional Loss SNV dbSNP153 33..33 33 - - - 67999 RMVar_ID_67999 Human_SNP_ID_685936921 m1A Human chr20 + 59686752 59686751 59686752 TGGTTATGATGATGGTGGTGATGATGGTGATGATGATGGTGATGATGATGGTGATGATGATGGTG TGGTTATGATGATGGTGGTGATGATGGTGATG_TGATGGTGATGATGATGGTGATGATGATGGTG GA G PHACTR3 Ensembl:ENSG00000087495 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:59686734..59686817 26863196 MeRIP-seq:(Medium) rs1568711632 Functional Loss DEL dbSNP153 33..33 33 - - - 68000 RMVar_ID_68000 Human_SNP_ID_685936923 m1A Human chr20 + 59686752 59686752 59686752 TGGTTATGATGATGGTGGTGATGATGGTGATGATGATGGTGATGATGATGGTGATGATGATGGTG TGGTTATGATGATGGTGGTGATGATGGTGATGGTGATGGTGATGATGATGGTGATGATGATGGTG A G PHACTR3 Ensembl:ENSG00000087495 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:59686734..59686817 26863196 MeRIP-seq:(Medium) rs988195088 Functional Loss SNV dbSNP153 33..33 33 - - - 68001 RMVar_ID_68001 Human_SNP_ID_686002650 m1A Human chr20 + 59933106 59933106 59933106 CCCCCCTTCAGATGTCCCGGAGACAGGCGAGCAGCGGTCCCCAGGGCTCCCGTCGCCACCGCTTC CCCCCCTTCAGATGTCCCGGAGACAGGCGAGCGGCGGTCCCCAGGGCTCCCGTCGCCACCGCTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59933058..59933207 26863196 MeRIP-seq:(Medium) rs1412741920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211120,RMVar_hsa_circ_211121,RMVar_hsa_circ_211122 68002 RMVar_ID_68002 Human_SNP_ID_686002677 m1A Human chr20 - 59933156 59933156 59933156 GGCCTGGGGCTGCGCGCGTCGCCGGCCCGAGGAGGCTGAGGGGTGCGGGAGAAGCGGTGGCGACG GGCCTGGGGCTGCGCGCGTCGCCGGCCCGAGGCGGCTGAGGGGTGCGGGAGAAGCGGTGGCGACG T G SYCP2 Ensembl:ENSG00000196074 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:59933114..59933431 26863196 MeRIP-seq:(Medium) rs1278528737 Functional Loss SNV dbSNP153 33..33 33 - - - 68003 RMVar_ID_68003 Human_SNP_ID_686002828 m1A Human chr20 - 59933476 59933476 59933476 GGCTTCGGCTTGGCCTTTCAAGCCGGCAGGCGAGAAGCTTCCGACGGTTGAGGCGGAGCCGTTGT GGCTTCGGCTTGGCCTTTCAAGCCGGCAGGCGGGAAGCTTCCGACGGTTGAGGCGGAGCCGTTGT T C SYCP2 Ensembl:ENSG00000196074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:59933356..59933479 26863196 MeRIP-seq:(Medium) rs1393945651 Functional Loss SNV dbSNP153 33..33 33 - - - 68004 RMVar_ID_68004 Human_SNP_ID_15527751 m1A Human chr1 + 61082452 61082441 61082452 TGCAGAGCGGAGGCGGAGGCGGGCGCGCGGGCAGCTCGCGGGCACCCGGCCGGGCCGGCGCGGGA TGCAGAGCGGAGGCGGAGGCGG___________GCTCGCGGGCACCCGGCCGGGCCGGCGCGGGA GGCGCGCGGGCA G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:61082403..61082835 26863196 MeRIP-seq:(Medium) rs1044530078 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_857677,Human_RBP_ID_4072855,Human_RBP_ID_18415556 RMVar_hsa_circ_88405,RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_133392 68005 RMVar_ID_68005 Human_SNP_ID_15655693 m1A Human chr1 + 61623725 61623725 61623725 GAGCTTGTCTCATCAATTGCTCCTAGTGTCCTATCCTACATCCTCAACCACCCTCTCCTTCTTTG GAGCTTGTCTCATCAATTGCTCCTAGTGTCCTGTCCTACATCCTCAACCACCCTCTCCTTCTTTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:61623643..61623727 26863196 MeRIP-seq:(Medium) rs535479267 Functional Loss SNV dbSNP153 33..33 33 - - - 68006 RMVar_ID_68006 Human_SNP_ID_15684386 m1A Human chr1 + 61742456 61742456 61742456 AGAGTCGGGGCGAGGGGAGGGCCTGCCAGGTGAGGCGCGGTCACCCTGGGCCTCTCACTTCCGCC AGAGTCGGGGCGAGGGGAGGGCCTGCCAGGTGGGGCGCGGTCACCCTGGGCCTCTCACTTCCGCC A G PATJ Ensembl:ENSG00000132849 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:61742407..61742645 26863196 MeRIP-seq:(Medium) rs1383258707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_78529,Human_Splice_Rec_78615,Human_Splice_Rec_78663,Human_Splice_Rec_78733,Human_Splice_Rec_78799,Human_Splice_Rec_78867,Human_Splice_Rec_78951,Human_Splice_Rec_78997 68007 RMVar_ID_68007 Human_SNP_ID_15684601 m1A Human chr1 - 61743029 61743029 61743029 CCTCACCCCGTTCCCTCCTTCCACGGCCACCGATGGAGGGAAAGACTCCGCCCAGCTCTGGGAGC CCTCACCCCGTTCCCTCCTTCCACGGCCACCGTTGGAGGGAAAGACTCCGCCCAGCTCTGGGAGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:61743009..61743116 26863196 MeRIP-seq:(Medium) rs897468680 Functional Loss SNV dbSNP153 33..33 33 - - - 68008 RMVar_ID_68008 Human_SNP_ID_15701695 m1A Human chr1 - 61812467 61812467 61812467 CGTCTCCAAGATGAGCACCCACCAATACCACCACACACACACACACACACACACACACACACACA CGTCTCCAAGATGAGCACCCACCAATACCACCCCACACACACACACACACACACACACACACACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:61812422..61812508 26863196 MeRIP-seq:(Medium) rs1471705526 Functional Loss SNV dbSNP153 33..33 33 - - - 68009 RMVar_ID_68009 Human_SNP_ID_15779777 m1A Human chr1 - 62143922 62143922 62143922 ATCCCCATCTCCCACCCAAACTTCCATGACCCACACTCTTCTGGCTTTCCTTCTGCAGGGGCCTG ATCCCCATCTCCCACCCAAACTTCCATGACCCCCACTCTTCTGGCTTTCCTTCTGCAGGGGCCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:62143873..62144060 26863196 MeRIP-seq:(Medium) rs985526341 Functional Loss SNV dbSNP153 33..33 33 - - - 68010 RMVar_ID_68010 Human_SNP_ID_15811461 m1A Human chr1 - 62253162 62253162 62253162 ACCATCAGAACAAAGCTGGCTACACTGCCGTAATGATCACTCCCTTGGCTTCCGCAGAGACCAAT ACCATCAGAACAAAGCTGGCTACACTGCCGTATTGATCACTCCCTTGGCTTCCGCAGAGACCAAT T A KANK4 Ensembl:ENSG00000132854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62253116..62253247 26863196 MeRIP-seq:(Medium) rs755326990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_79262,Human_Splice_Rec_79263,Human_Splice_Rec_79268,Human_Splice_Rec_79269,Human_Splice_Rec_79280,Human_Splice_Rec_79281,Human_Splice_Rec_79296,Human_Splice_Rec_79297 RMVar_hsa_circ_18709,RMVar_hsa_circ_373374,RMVar_hsa_circ_374370,RMVar_hsa_circ_335173,RMVar_hsa_circ_133482,RMVar_hsa_circ_133483,RMVar_hsa_circ_133484,RMVar_hsa_circ_13068 68011 RMVar_ID_68011 Human_SNP_ID_15811462 m1A Human chr1 - 62253162 62253162 62253162 ACCATCAGAACAAAGCTGGCTACACTGCCGTAATGATCACTCCCTTGGCTTCCGCAGAGACCAAT ACCATCAGAACAAAGCTGGCTACACTGCCGTAGTGATCACTCCCTTGGCTTCCGCAGAGACCAAT T C KANK4 Ensembl:ENSG00000132854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62253116..62253247 26863196 MeRIP-seq:(Medium) rs755326990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_79262,Human_Splice_Rec_79263,Human_Splice_Rec_79268,Human_Splice_Rec_79269,Human_Splice_Rec_79280,Human_Splice_Rec_79281,Human_Splice_Rec_79296,Human_Splice_Rec_79297 RMVar_hsa_circ_18709,RMVar_hsa_circ_373374,RMVar_hsa_circ_374370,RMVar_hsa_circ_335173,RMVar_hsa_circ_133482,RMVar_hsa_circ_133483,RMVar_hsa_circ_133484,RMVar_hsa_circ_13068 68012 RMVar_ID_68012 Human_SNP_ID_15814705 m1A Human chr1 + 62266519 62266517 62266519 CTGCCTCACACACACACCACTCACACCACTGCACACTCACACCACTGCCTCACACTGCACACTCA CTGCCTCACACACACACCACTCACACCACTG__CACTCACACCACTGCCTCACACTGCACACTCA GCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:62266419..62266548 26863196 MeRIP-seq:(Medium) rs1244576854 Functional Loss DEL dbSNP153 32..33 33 - - - 68013 RMVar_ID_68013 Human_SNP_ID_15816601 m1A Human chr1 - 62273764 62273764 62273764 TCTAGGCAGCATGGAGTCTGAAAGCTGGGGGCACCGAGGAGAGGAGAATGGCCTCCTATGGGGGC TCTAGGCAGCATGGAGTCTGAAAGCTGGGGGCTCCGAGGAGAGGAGAATGGCCTCCTATGGGGGC T A KANK4 Ensembl:ENSG00000132854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62273713..62273838 26863196 MeRIP-seq:(Medium) rs1275788397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64553 68014 RMVar_ID_68014 Human_SNP_ID_15817001 m1A Human chr1 - 62274790 62274790 62274790 GGTGCCAAGGGAGGCATCACTTGGGACACAGGAGCAAAACCAGTCACCACCGCTTGGTAATGCCC GGTGCCAAGGGAGGCATCACTTGGGACACAGGTGCAAAACCAGTCACCACCGCTTGGTAATGCCC T A KANK4 Ensembl:ENSG00000132854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62274739..62274837 26863196 MeRIP-seq:(Medium) rs774160002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64553 68015 RMVar_ID_68015 Human_SNP_ID_15827279 m1A Human chr1 - 62319241 62319226 62319242 GGTGTGCGCGCCGCGGACGACCAGGGTGCGCCAGCCCCGGGGTGCGCGCCTGGGACGCGGACAGT GGTGTGCGCGCCGCGGACGACCAGGGTGCGC________________GCCTGGGACGCGGACAGT CGCGCACCCCGGGGCTG C KANK4 Ensembl:ENSG00000132854 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:62319193..62319385 26863196 MeRIP-seq:(Medium) rs1421389510 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_4072858,Human_RBP_ID_9352500 68016 RMVar_ID_68016 Human_SNP_ID_15855981 m1A Human chr1 + 62439777 62439777 62439777 TTGTTGCCAAAACTGATAACCAAAAACTAATGAAACTTTCTCTGTGATTAACAGATATAATTGGT TTGTTGCCAAAACTGATAACCAAAAACTAATGCAACTTTCTCTGTGATTAACAGATATAATTGGT A C USP1 Ensembl:ENSG00000162607 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:62439776..62439850 26863196 MeRIP-seq:(Medium) rs550973893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22637093 RMVar_hsa_circ_133487,RMVar_hsa_circ_107857 68017 RMVar_ID_68017 Human_SNP_ID_15859089 m1A Human chr1 - 62450502 62450502 62450502 CTCAACCACACCCCTTGCTTCCTCCTCATTCAATGGTTCTGGCTTACCTATTTCACACATTTGGT CTCAACCACACCCCTTGCTTCCTCCTCATTCAGTGGTTCTGGCTTACCTATTTCACACATTTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:62450451..62450625 26863196 MeRIP-seq:(Medium) rs770818820 Functional Loss SNV dbSNP153 33..33 33 - - - 68018 RMVar_ID_68018 Human_SNP_ID_15916552 m1A Human chr1 - 62688257 62688257 62688257 CGCCGTCGCCGTCGCCGCAGCAGCCATGGCCGAGCGCCGCGCCTTCGCCCAGAAGATCAGCAGGT CGCCGTCGCCGTCGCCGCAGCAGCCATGGCCGCGCGCCGCGCCTTCGCCCAGAAGATCAGCAGGT T G DOCK7 Ensembl:ENSG00000116641 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:62688241..62688328 26863410 MeRIP-seq:(Medium) rs1381485913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221417,Human_RBP_ID_804185 Human_Splice_Rec_79359,Human_Splice_Rec_79457,Human_Splice_Rec_79555,Human_Splice_Rec_79683,Human_Splice_Rec_79835,Human_Splice_Rec_79931,Human_Splice_Rec_80057,Human_Splice_Rec_80189,Human_Splice_Rec_80273 RMVar_hsa_circ_83708,RMVar_hsa_circ_133520 68019 RMVar_ID_68019 Human_SNP_ID_16067555 m1A Human chr1 - 63322412 63322412 63322412 AAAGGGACGAGAGACGCGCAACTCCGCTCCGCACTGTGCGCCAGCATCCCCGGGGCACGGAGGGC AAAGGGACGAGAGACGCGCAACTCCGCTCCGCGCTGTGCGCCAGCATCCCCGGGGCACGGAGGGC T C FOXD3-AS1 Ensembl:ENSG00000230798 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63322300..63322453 26863196 MeRIP-seq:(Medium) rs975627930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_80789,Human_Splice_Rec_80793 Human_miRNA_ID_3149674,Human_miRNA_ID_3163066,Human_miRNA_ID_3179403 68020 RMVar_ID_68020 Human_SNP_ID_16068365 m1A Human chr1 + 63324336 63324336 63324336 TTTCTGCGGCCACCCGGGACCGTGCAGTCGGCAGCGCTCATGGCCACCCACCAACCGCTGTCGCT TTTCTGCGGCCACCCGGGACCGTGCAGTCGGCGGCGCTCATGGCCACCCACCAACCGCTGTCGCT A G FOXD3 Ensembl:ENSG00000187140 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:63324296..63324383 26863196 MeRIP-seq:(Medium) rs750861704 Functional Loss SNV dbSNP153 33..33 33 - - - 68021 RMVar_ID_68021 Human_SNP_ID_16068518 m1A Human chr1 + 63324648 63324648 63324648 CTCTCCCCAATTTCCTTTCCCCTGAGCCCCCAACGCCTACCTTCCGCGGCCTCCATCCCCTCGCG CTCTCCCCAATTTCCTTTCCCCTGAGCCCCCACCGCCTACCTTCCGCGGCCTCCATCCCCTCGCG A C FOXD3 Ensembl:ENSG00000187140 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:63324598..63324709 26863196 MeRIP-seq:(Medium) rs1324484594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224682,Human_RBP_ID_23406818 68022 RMVar_ID_68022 Human_SNP_ID_16068519 m1A Human chr1 + 63324648 63324648 63324648 CTCTCCCCAATTTCCTTTCCCCTGAGCCCCCAACGCCTACCTTCCGCGGCCTCCATCCCCTCGCG CTCTCCCCAATTTCCTTTCCCCTGAGCCCCCAGCGCCTACCTTCCGCGGCCTCCATCCCCTCGCG A G FOXD3 Ensembl:ENSG00000187140 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:63324598..63324709 26863196 MeRIP-seq:(Medium) rs1324484594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224682,Human_RBP_ID_23406818 68023 RMVar_ID_68023 Human_SNP_ID_16079390 m1A Human chr1 - 63367689 63367689 63367689 GGGGTCCGGAACCTCCGGGATCCCATGCTCTTACCCCGCCGCCCGCCGGCCGCTGGGATTCGCGC GGGGTCCGGAACCTCCGGGATCCCATGCTCTTCCCCCGCCGCCCGCCGGCCGCTGGGATTCGCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:63367658..63367747;chr1:63367669..63367766 26863196 MeRIP-seq:(Medium) rs940418404 Functional Loss SNV dbSNP153 33..33 33 - - - 68024 RMVar_ID_68024 Human_SNP_ID_16093540 m1A Human chr1 + 63426276 63426276 63426276 GAGAGGGAGAACTGGTAGGAAAGTAGTGAGGAAGATCAAGGAGGTTACTTCCCACCATCAGGCCA GAGAGGGAGAACTGGTAGGAAAGTAGTGAGGATGATCAAGGAGGTTACTTCCCACCATCAGGCCA A T ALG6 Ensembl:ENSG00000088035 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63425800..63426453 26863196 MeRIP-seq:(Medium) rs987710625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5850665 RMVar_hsa_circ_34288,RMVar_hsa_circ_323317,RMVar_hsa_circ_304283,RMVar_hsa_circ_133590,RMVar_hsa_circ_133591 68025 RMVar_ID_68025 Human_SNP_ID_16132146 m1A Human chr1 - 63593454 63593454 63593454 TGGCGACTTGCTGCCGGGGGTCAGAGCGGCGGACTTGGCTGGCGGAGGGGCGGCCGGCTGAGGCT TGGCGACTTGCTGCCGGGGGTCAGAGCGGCGGTCTTGGCTGGCGGAGGGGCGGCCGGCTGAGGCT T A ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:63593326..63593700 26863410 MeRIP-seq:(Medium) rs756324880 Functional Loss SNV dbSNP153 33..33 33 - - - 68026 RMVar_ID_68026 Human_SNP_ID_16142320 m1A Human chr1 + 63634928 63634928 63634928 CTGCGTTCCTCTGGAGGACTTTGGAGGCCACCACCCTGACCCCAACCTCACCTATGCAGCTGACC CTGCGTTCCTCTGGAGGACTTTGGAGGCCACCGCCCTGACCCCAACCTCACCTATGCAGCTGACC A G PGM1 Ensembl:ENSG00000079739 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:63634879..63635047 26863196 MeRIP-seq:(Medium) rs1164462551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18968505 Human_Splice_Rec_81166,Human_Splice_Rec_81167,Human_Splice_Rec_81184,Human_Splice_Rec_81185,Human_Splice_Rec_81202,Human_Splice_Rec_81203,Human_Splice_Rec_81222,Human_Splice_Rec_81223 Human_miRNA_ID_2006168,Human_miRNA_ID_2006169 RMVar_hsa_circ_85104,RMVar_hsa_circ_88997,RMVar_hsa_circ_133611,RMVar_hsa_circ_133609,RMVar_hsa_circ_133610,RMVar_hsa_circ_299954,RMVar_hsa_circ_310052,RMVar_hsa_circ_369039,RMVar_hsa_circ_133612,RMVar_hsa_circ_65619,RMVar_hsa_circ_22049,RMVar_hsa_circ_72555 68027 RMVar_ID_68027 Human_SNP_ID_16142340 m1A Human chr1 + 63634972 63634972 63634972 ACCTCACCTATGCAGCTGACCTGGTGGAGACCATGAAGTCAGGAGAGCATGATTTTGGGGCTGCC ACCTCACCTATGCAGCTGACCTGGTGGAGACCCTGAAGTCAGGAGAGCATGATTTTGGGGCTGCC A C PGM1 Ensembl:ENSG00000079739 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:63631727..63634974 32194978 MeRIP-seq:(Medium) rs147596060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18965650 Human_Splice_Rec_81167,Human_Splice_Rec_81185,Human_Splice_Rec_81203,Human_Splice_Rec_81223 RMVar_hsa_circ_85104,RMVar_hsa_circ_88997,RMVar_hsa_circ_133611,RMVar_hsa_circ_133609,RMVar_hsa_circ_133610,RMVar_hsa_circ_299954,RMVar_hsa_circ_310052,RMVar_hsa_circ_369039,RMVar_hsa_circ_133612,RMVar_hsa_circ_65619,RMVar_hsa_circ_22049,RMVar_hsa_circ_72555 68028 RMVar_ID_68028 Human_SNP_ID_16142341 m1A Human chr1 + 63634972 63634972 63634972 ACCTCACCTATGCAGCTGACCTGGTGGAGACCATGAAGTCAGGAGAGCATGATTTTGGGGCTGCC ACCTCACCTATGCAGCTGACCTGGTGGAGACCGTGAAGTCAGGAGAGCATGATTTTGGGGCTGCC A G PGM1 Ensembl:ENSG00000079739 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:63631727..63634974 32194978 MeRIP-seq:(Medium) rs147596060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18965650 Human_Splice_Rec_81167,Human_Splice_Rec_81185,Human_Splice_Rec_81203,Human_Splice_Rec_81223 RMVar_hsa_circ_85104,RMVar_hsa_circ_88997,RMVar_hsa_circ_133611,RMVar_hsa_circ_133609,RMVar_hsa_circ_133610,RMVar_hsa_circ_299954,RMVar_hsa_circ_310052,RMVar_hsa_circ_369039,RMVar_hsa_circ_133612,RMVar_hsa_circ_65619,RMVar_hsa_circ_22049,RMVar_hsa_circ_72555 68029 RMVar_ID_68029 Human_SNP_ID_16146231 m1A Human chr1 - 63651721 63651721 63651721 CACAAAGGAGCGATCAAACATCAGGGCCTCCAAGTCCTTCATCATTTTGTTTGCGCCCTCAGCTT CACAAAGGAGCGATCAAACATCAGGGCCTCCAGGTCCTTCATCATTTTGTTTGCGCCCTCAGCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:63651626..63651794 26863196 MeRIP-seq:(Medium) rs1380342652 Functional Loss SNV dbSNP153 33..33 33 - - - 68030 RMVar_ID_68030 Human_SNP_ID_16146860 m1A Human chr1 - 63654355 63654355 63654355 GTGCCGCTCAGTCGGAAGACGATTCGAGAACCATCTGTGAAAATGAGGCGCAAGCCCTGGAAAAG GTGCCGCTCAGTCGGAAGACGATTCGAGAACCGTCTGTGAAAATGAGGCGCAAGCCCTGGAAAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:63651826..63659946 32194978 MeRIP-seq:(Medium) rs1057519218 Functional Loss SNV dbSNP153 33..33 33 - - - 68031 RMVar_ID_68031 Human_SNP_ID_16174938 m1A Human chr1 + 63774255 63774255 63774255 CGCGCTCGCGGCATCCAGAGGCGGCCAGGCGGAGGCGAGGGAGCAGGTTAGAGGGACAAAGAGCT CGCGCTCGCGGCATCCAGAGGCGGCCAGGCGGCGGCGAGGGAGCAGGTTAGAGGGACAAAGAGCT A C ROR1 Ensembl:ENSG00000185483 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:63773994..63774489 26863196 MeRIP-seq:(Medium) rs1163464797 Functional Loss SNV dbSNP153 33..33 33 - - - 68032 RMVar_ID_68032 Human_SNP_ID_16187323 m1A Human chr1 - 63829450 63829450 63829450 GGAAGCCTTCCAGGGTCCTGTCCCCACATCTGAATTAGGAATCCCTCGTGACGGTGCTCCCATAG GGAAGCCTTCCAGGGTCCTGTCCCCACATCTGTATTAGGAATCCCTCGTGACGGTGCTCCCATAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:63829437..63829575 26863196 MeRIP-seq:(Medium) rs916372379 Functional Loss SNV dbSNP153 33..33 33 - - - 68033 RMVar_ID_68033 Human_SNP_ID_16207298 m1A Human chr1 + 63920326 63920326 63920326 AAGCACTGGTGATGGGAGGAGGGATTTATTTGAGCTGGTTTTTCAAAGGATGGGTAAGGAAAGAA AAGCACTGGTGATGGGAGGAGGGATTTATTTGGGCTGGTTTTTCAAAGGATGGGTAAGGAAAGAA A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63920320..63920435 26863196 MeRIP-seq:(Medium) rs1015190745 Functional Loss SNV dbSNP153 33..33 33 - - - 68034 RMVar_ID_68034 Human_SNP_ID_16210104 m1A Human chr1 - 63932253 63932253 63932253 GGGCCCCCATAGGCCAGCCAAGAATCCTATCTATCACCCCTGCACCTTTTCCACCTCTTCCTCCC GGGCCCCCATAGGCCAGCCAAGAATCCTATCTGTCACCCCTGCACCTTTTCCACCTCTTCCTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63932240..63932345 26863196 MeRIP-seq:(Medium) rs1478166979 Functional Loss SNV dbSNP153 33..33 33 - - - 68035 RMVar_ID_68035 Human_SNP_ID_16214518 m1A Human chr1 + 63952165 63952165 63952165 AGTGTAGCTGTTTTGTAAGGGATGGGAAAGGAAGGGCTCTCACAGTTCTGGTCTGAGCTGAGATC AGTGTAGCTGTTTTGTAAGGGATGGGAAAGGAGGGGCTCTCACAGTTCTGGTCTGAGCTGAGATC A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63952155..63952261 26863196 MeRIP-seq:(Medium) rs1237022851 Functional Loss SNV dbSNP153 33..33 33 - - - 68036 RMVar_ID_68036 Human_SNP_ID_16216836 m1A Human chr1 + 63962589 63962589 63962589 AGAAAAGCCTCCCTGGAGTTGGTGATGATTTAACTGCATCTCAAATAATGATCAGACATCCATCA AGAAAAGCCTCCCTGGAGTTGGTGATGATTTAGCTGCATCTCAAATAATGATCAGACATCCATCA A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63962583..63962876 26863196 MeRIP-seq:(Medium) rs1048044400 Functional Loss SNV dbSNP153 33..33 33 - - - 68037 RMVar_ID_68037 Human_SNP_ID_16227091 m1A Human chr1 - 64009271 64009271 64009271 TGAAAAGAAAAAGAAGGGAAGGGAGAAAGACAAGGGCAATATTAAATATAGTAATTTATAGGCTG TGAAAAGAAAAAGAAGGGAAGGGAGAAAGACATGGGCAATATTAAATATAGTAATTTATAGGCTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:64009266..64009334 26863196 MeRIP-seq:(Medium) rs779892615 Functional Loss SNV dbSNP153 33..33 33 - - - 68038 RMVar_ID_68038 Human_SNP_ID_16257399 m1A Human chr1 + 64143867 64143867 64143867 GACTTAAGCTTTGACGCTGAATGAGTTGGGAAAGCATGAGAGGGTTTTGAGCAGAAGGGTGACAT GACTTAAGCTTTGACGCTGAATGAGTTGGGAAGGCATGAGAGGGTTTTGAGCAGAAGGGTGACAT A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:64143715..64143884 26863196 MeRIP-seq:(Medium) rs1470139215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23407465 RMVar_hsa_circ_363351 68039 RMVar_ID_68039 Human_SNP_ID_16336120 m1A Human chr1 - 64470435 64470435 64470435 CAGAGGGCGTCTCCGAGAGCAGGGGCGCCCGCAGGCCGGGGTGCGCGGGCCCCGGGGCTGACAGT CAGAGGGCGTCTCCGAGAGCAGGGGCGCCCGCGGGCCGGGGTGCGCGGGCCCCGGGGCTGACAGT T C HSALNG0004159 RNACentral:URS0000EBFC31 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:64470226..64470497 26863410 MeRIP-seq:(Medium) rs1175263910 Functional Loss SNV dbSNP153 33..33 33 - - - 68040 RMVar_ID_68040 Human_SNP_ID_16425886 m1A Human chr1 + 64860159 64860159 64860159 TCTGTATGTTGTGGACGATCAACGGGGGGGCCACGTCGGTGCAGAGGTAATGATGGGCATCTGCT TCTGTATGTTGTGGACGATCAACGGGGGGGCCGCGTCGGTGCAGAGGTAATGATGGGCATCTGCT A G lnc-AK4-1 RNACentral:URS0000D5D7C7 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:64860086..64866952 32194978 MeRIP-seq:(Medium) rs1331579419 Functional Loss SNV dbSNP153 33..33 33 - - - 68041 RMVar_ID_68041 Human_SNP_ID_16441287 m1A Human chr1 - 64926199 64926199 64926199 ACAATAGCACTGGCCGTAGGAGAGAGGCAGGAACTGGAGTGAAGATAGGTTAGAGCCAGCACTCA ACAATAGCACTGGCCGTAGGAGAGAGGCAGGAGCTGGAGTGAAGATAGGTTAGAGCCAGCACTCA T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:64926194..64926508 26863196 MeRIP-seq:(Medium) rs1025290816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5853000,Human_RBP_ID_11073429 RMVar_hsa_circ_123711,RMVar_hsa_circ_133664 68042 RMVar_ID_68042 Human_SNP_ID_16441443 m1A Human chr1 - 64927062 64927062 64927062 AGCAGTCAGGGCTGAAGAGTCAGCTTGGACAAAGGTGGGAAGTAGTTGGTATATTTGAGGACATA AGCAGTCAGGGCTGAAGAGTCAGCTTGGACAAGGGTGGGAAGTAGTTGGTATATTTGAGGACATA T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:64927056..64927139 26863196 MeRIP-seq:(Medium) rs12031995 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8125,GWAS_ID_8126,GWAS_ID_8127 RMVar_hsa_circ_123711,RMVar_hsa_circ_133664 68043 RMVar_ID_68043 Human_SNP_ID_16448401 m1A Human chr1 + 64956532 64956531 64956532 TCTCAGACCAGGAGCCCTTCTCCCAACCCCCCAACCTAAGCATTCACTACCCATACCTTGCTAAC TCTCAGACCAGGAGCCCTTCTCCCAACCCCCC_ACCTAAGCATTCACTACCCATACCTTGCTAAC CA C lnc-AK4-1 RNACentral:URS0000D5D7C7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:64956530..64956650 26863196 MeRIP-seq:(Medium) rs1490846537 Functional Loss DEL dbSNP153 33..33 33 - - - 68044 RMVar_ID_68044 Human_SNP_ID_16448402 m1A Human chr1 + 64956532 64956532 64956532 TCTCAGACCAGGAGCCCTTCTCCCAACCCCCCAACCTAAGCATTCACTACCCATACCTTGCTAAC TCTCAGACCAGGAGCCCTTCTCCCAACCCCCCCACCTAAGCATTCACTACCCATACCTTGCTAAC A C lnc-AK4-1 RNACentral:URS0000D5D7C7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:64956530..64956650 26863196 MeRIP-seq:(Medium) rs1238955018 Functional Loss SNV dbSNP153 33..33 33 - - - 68045 RMVar_ID_68045 Human_SNP_ID_16449533 m1A Human chr1 - 64961566 64961566 64961566 ACTGCTTGGGAGGGAGCGGAAGGAGGTAGGGCAGGACATGCAGGTTGGATCCAGATTGTGAAGAC ACTGCTTGGGAGGGAGCGGAAGGAGGTAGGGCGGGACATGCAGGTTGGATCCAGATTGTGAAGAC T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:64961564..64961664;chr1:64961557..64961717 26863196 MeRIP-seq:(Medium) rs986108580 Functional Loss SNV dbSNP153 33..33 33 - - - 68046 RMVar_ID_68046 Human_SNP_ID_16494848 m1A Human chr1 - 65148211 65148211 65148211 CTCCCCTCAGCCCAGCGCCGGGACCGAGTAGCAGGCGGACTGAGCGCCACGCTACACCTCCCCGC CTCCCCTCAGCCCAGCGCCGGGACCGAGTAGCGGGCGGACTGAGCGCCACGCTACACCTCCCCGC T C lnc-JAK1-7 RNACentral:URS00008C03CB lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:65148164..65148289 26863196 MeRIP-seq:(Medium) rs564944065 Functional Loss SNV dbSNP153 33..33 33 - - - 68047 RMVar_ID_68047 Human_SNP_ID_16520910 m1A Human chr1 + 65254519 65254478 65254519 GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGAGGGCGCGGCGCACCGATGGGCGCCACTGAGAA _________________________________GGGCGCGGCGCACCGATGGGCGCCACTGAGAA CGGCGAGCGGTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGA C DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:65254470..65254625;chr1:65254472..65254636 26863196 MeRIP-seq:(Medium) rs1280453507 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_744663,Human_RBP_ID_4063090,Human_RBP_ID_5312577,Human_RBP_ID_8755027,Human_RBP_ID_9318988,Human_RBP_ID_22871316 68048 RMVar_ID_68048 Human_SNP_ID_16520937 m1A Human chr1 + 65254519 65254519 65254519 GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGAGGGCGCGGCGCACCGATGGGCGCCACTGAGAA GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGCGGGCGCGGCGCACCGATGGGCGCCACTGAGAA A C DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:65254470..65254625;chr1:65254472..65254636 26863196 MeRIP-seq:(Medium) rs905058342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744663,Human_RBP_ID_4063090,Human_RBP_ID_5312577,Human_RBP_ID_8755027,Human_RBP_ID_9318988,Human_RBP_ID_22871316 68049 RMVar_ID_68049 Human_SNP_ID_16520938 m1A Human chr1 + 65254519 65254519 65254519 GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGAGGGCGCGGCGCACCGATGGGCGCCACTGAGAA GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGGGGGCGCGGCGCACCGATGGGCGCCACTGAGAA A G DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:65254470..65254625;chr1:65254472..65254636 26863196 MeRIP-seq:(Medium) rs905058342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744663,Human_RBP_ID_4063090,Human_RBP_ID_5312577,Human_RBP_ID_8755027,Human_RBP_ID_9318988,Human_RBP_ID_22871316 68050 RMVar_ID_68050 Human_SNP_ID_16544443 m1A Human chr1 - 65360829 65360829 65360829 CATAAATCACTGCATGCCAGGCAAACCAAGTCAATCTCATTACGCAGGCAGCCGAGCCTCTGTCG CATAAATCACTGCATGCCAGGCAAACCAAGTCCATCTCATTACGCAGGCAGCCGAGCCTCTGTCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:65360827..65360959 26863196 MeRIP-seq:(Medium) rs1015706656 Functional Loss SNV dbSNP153 33..33 33 - - - 68051 RMVar_ID_68051 Human_SNP_ID_16545261 m1A Human chr1 + 65364594 65364594 65364594 AAGAGGGATTGGTTTTCCGTGGATTCTCTGCCATCACCATTTTTGTTTGTTTGTTTTTTTTTTTT AAGAGGGATTGGTTTTCCGTGGATTCTCTGCCGTCACCATTTTTGTTTGTTTGTTTTTTTTTTTT A G DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:65364590..65364656 26863196 MeRIP-seq:(Medium) rs1177999792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133689,RMVar_hsa_circ_288222 68052 RMVar_ID_68052 Human_SNP_ID_16552380 m1A Human chr1 + 65395004 65395004 65395004 TCCAGTGCTTCCAGTGACCCCTTTCTCCAGCCAACAAGAAGTCCTTCGCCCACAGTACATGGTAA TCCAGTGCTTCCAGTGACCCCTTTCTCCAGCCCACAAGAAGTCCTTCGCCCACAGTACATGGTAA A C DNAJC6 Ensembl:ENSG00000116675 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4582839 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3933625,Human_RBP_ID_22559424 Human_Splice_Rec_82711,Human_Splice_Rec_82747,Human_Splice_Rec_82787 GWAS_ID_8128,GWAS_ID_8129,GWAS_ID_8130,GWAS_ID_8131 RMVar_hsa_circ_314738,RMVar_hsa_circ_348663,RMVar_hsa_circ_319680,RMVar_hsa_circ_314537,RMVar_hsa_circ_117635,RMVar_hsa_circ_133691,RMVar_hsa_circ_133692,RMVar_hsa_circ_133690,RMVar_hsa_circ_43617,RMVar_hsa_circ_343019,RMVar_hsa_circ_29406,RMVar_hsa_circ_42839 68053 RMVar_ID_68053 Human_SNP_ID_16559649 m1A Human chr1 - 65426433 65426433 65426433 GAATGACATTTTAACATAACCCCCTCCTCCAAACCCATTCTCAAGATATTTTCCCAGGTTCTATT GAATGACATTTTAACATAACCCCCTCCTCCAAGCCCATTCTCAAGATATTTTCCCAGGTTCTATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:65426428..65426577 26863196 MeRIP-seq:(Medium) rs977230680 Functional Loss SNV dbSNP153 33..33 33 - - - 68054 RMVar_ID_68054 Human_SNP_ID_16561457 m1A Human chr1 + 65433682 65433682 65433682 TTTTCAGTGTCCTGTGTACATATAGAATTGTTAAAGTTGTCATTTCCAATATTTATATTAGAAAA TTTTCAGTGTCCTGTGTACATATAGAATTGTTGAAGTTGTCATTTCCAATATTTATATTAGAAAA A G LEPROT,LEPR Ensembl:ENSG00000213625,Ensembl:ENSG00000116678 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs990463181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18302,Human_RBP_ID_1752607,Human_RBP_ID_5137147,Human_RBP_ID_21880160,Human_RBP_ID_26391129 RMVar_hsa_circ_83274,RMVar_hsa_circ_367796,RMVar_hsa_circ_106328,RMVar_hsa_circ_133704,RMVar_hsa_circ_133703,RMVar_hsa_circ_84483,RMVar_hsa_circ_133706 68055 RMVar_ID_68055 Human_SNP_ID_16563150 m1A Human chr1 - 65440581 65440581 65440581 CTTTTTGAACCATCTTGCCCATTGCCGCCTCCATAACTGCCTCTACTTCCTTCAAACGTCATCTT CTTTTTGAACCATCTTGCCCATTGCCGCCTCCGTAACTGCCTCTACTTCCTTCAAACGTCATCTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:65440417..65440613 26863196 MeRIP-seq:(Medium) rs1261315836 Functional Loss SNV dbSNP153 33..33 33 - - - 68056 RMVar_ID_68056 Human_SNP_ID_16599579 m1A Human chr1 + 65592830 65592830 65592830 TTTGAAAATCACATCTGGTGGAGTAATTTTCCAGTCACCTCTAATGTCAGTTCAGCCCATAAATA TTTGAAAATCACATCTGGTGGAGTAATTTTCCGGTCACCTCTAATGTCAGTTCAGCCCATAAATA A G LEPR Ensembl:ENSG00000116678 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137101 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_979450 Human_Splice_Rec_82851,Human_Splice_Rec_82889,Human_Splice_Rec_82927,Human_Splice_Rec_82963,Human_Splice_Rec_82987,Human_Splice_Rec_83023,Human_Splice_Rec_83057 Human_miRNA_ID_250040,Human_miRNA_ID_820188,Human_miRNA_ID_2346835 Clinvar_Rec_275 GWAS_ID_8132,GWAS_ID_8133,GWAS_ID_8134,GWAS_ID_8135,GWAS_ID_8136,GWAS_ID_8137,GWAS_ID_8138,GWAS_ID_8139,GWAS_ID_8140,GWAS_ID_8141,GWAS_ID_8142,GWAS_ID_8143,GWAS_ID_8144,GWAS_ID_8145,GWAS_ID_8146,GWAS_ID_8147,GWAS_ID_8148,GWAS_ID_8149,GWAS_ID_8150,GWAS_ID_8151,GWAS_ID_8152,GWAS_ID_8153,GWAS_ID_8154,GWAS_ID_8155,GWAS_ID_8156,GWAS_ID_8157,GWAS_ID_8158,GWAS_ID_8159,GWAS_ID_8160,GWAS_ID_8161,GWAS_ID_8162,GWAS_ID_8163,GWAS_ID_8164,GWAS_ID_8165,GWAS_ID_8166,GWAS_ID_8167,GWAS_ID_8168,GWAS_ID_8169,GWAS_ID_8170,GWAS_ID_8171,GWAS_ID_8172,GWAS_ID_8173,GWAS_ID_8174,GWAS_ID_8175,GWAS_ID_8176,GWAS_ID_8177,GWAS_ID_8178,GWAS_ID_8179,GWAS_ID_8180,GWAS_ID_8181,GWAS_ID_8182,GWAS_ID_8183,GWAS_ID_8184,GWAS_ID_8185,GWAS_ID_8186,GWAS_ID_8187,GWAS_ID_8188,GWAS_ID_8189,GWAS_ID_8190,GWAS_ID_8191,GWAS_ID_8192,GWAS_ID_8193,GWAS_ID_8194,GWAS_ID_8195,GWAS_ID_8196,GWAS_ID_8197,GWAS_ID_8198,GWAS_ID_8199,GWAS_ID_8200,GWAS_ID_8201,GWAS_ID_8202,GWAS_ID_8203,GWAS_ID_8204,GWAS_ID_8205,GWAS_ID_8206,GWAS_ID_8207,GWAS_ID_8208,GWAS_ID_8209,GWAS_ID_8210,GWAS_ID_8211,GWAS_ID_8212,GWAS_ID_8213,GWAS_ID_8214,GWAS_ID_8215 RMVar_hsa_circ_106328,RMVar_hsa_circ_133704,RMVar_hsa_circ_6206,RMVar_hsa_circ_10323,RMVar_hsa_circ_331632,RMVar_hsa_circ_120263,RMVar_hsa_circ_60486,RMVar_hsa_circ_356016,RMVar_hsa_circ_133709,RMVar_hsa_circ_61633,RMVar_hsa_circ_14004,RMVar_hsa_circ_68766,RMVar_hsa_circ_350358,RMVar_hsa_circ_356483,RMVar_hsa_circ_366373,RMVar_hsa_circ_91754,RMVar_hsa_circ_133710 68057 RMVar_ID_68057 Human_SNP_ID_16920157 m1A Human chr1 + 66925046 66925031 66925046 CCCGGCTGCAGGCGGATGGATGGGGCTTCTTCAGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG CCCGGCTGCAGGCGGATG_______________GGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG GGATGGGGCTTCTTCA G MIER1 Ensembl:ENSG00000198160 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:66924874..66925165;chr1:66924960..66925175 26863196 MeRIP-seq:(Medium) rs1292099512 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_4074110,Human_RBP_ID_18968509 Human_Splice_Rec_83705,Human_Splice_Rec_83731,Human_Splice_Rec_83761,Human_Splice_Rec_83789,Human_Splice_Rec_83815,Human_Splice_Rec_83845,Human_Splice_Rec_83873 68058 RMVar_ID_68058 Human_SNP_ID_16920161 m1A Human chr1 + 66925046 66925046 66925046 CCCGGCTGCAGGCGGATGGATGGGGCTTCTTCAGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG CCCGGCTGCAGGCGGATGGATGGGGCTTCTTCTGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG A T MIER1 Ensembl:ENSG00000198160 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:66924874..66925165;chr1:66924960..66925175 26863196 MeRIP-seq:(Medium) rs1015161479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074110,Human_RBP_ID_18968509 Human_Splice_Rec_83705,Human_Splice_Rec_83731,Human_Splice_Rec_83761,Human_Splice_Rec_83789,Human_Splice_Rec_83815,Human_Splice_Rec_83845,Human_Splice_Rec_83873 68059 RMVar_ID_68059 Human_SNP_ID_16920173 m1A Human chr1 + 66925062 66925062 66925062 TGGATGGGGCTTCTTCAGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGGCAGCAGCGGCAGCGGC TGGATGGGGCTTCTTCAGGCGGTGGCGGCAGCCGCGAAGGTGGCGGCGGCAGCAGCGGCAGCGGC A C MIER1 Ensembl:ENSG00000198160 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:66924979..66925160 26863196 MeRIP-seq:(Medium) rs939345723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074110,Human_RBP_ID_18968509 Human_Splice_Rec_83705,Human_Splice_Rec_83731,Human_Splice_Rec_83761,Human_Splice_Rec_83789,Human_Splice_Rec_83815,Human_Splice_Rec_83845,Human_Splice_Rec_83873 68060 RMVar_ID_68060 Human_SNP_ID_16920249 m1A Human chr1 - 66925242 66925242 66925242 CGGCGGAGAGCAAGCCAGGCGCGTTCTGCGGCAGCCCCTCCCCGGAAGTTAAGGGTCTTCCGGGC CGGCGGAGAGCAAGCCAGGCGCGTTCTGCGGCGGCCCCTCCCCGGAAGTTAAGGGTCTTCCGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:66925236..66925373 26863196 MeRIP-seq:(Medium) rs1362895171 Functional Loss SNV dbSNP153 33..33 33 - - - 68061 RMVar_ID_68061 Human_SNP_ID_16928837 m1A Human chr1 - 66958178 66958178 66958178 CCACTACAGCCACTGTTGTCATCATTATCAGCATCTTCATCATCTTCACCTTCTTCTTCCTCTTC CCACTACAGCCACTGTTGTCATCATTATCAGCTTCTTCATCATCTTCACCTTCTTCTTCCTCTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:66958098..66958179 26863196 MeRIP-seq:(Medium) rs1306879667 Functional Loss SNV dbSNP153 33..33 33 - - - 68062 RMVar_ID_68062 Human_SNP_ID_17038252 m1A Human chr1 - 67409731 67409731 67409731 CAGCTTCCCAGAAATTTGGGTTATTTGGCCTAAGCTGTGCCCTGGGATTACCTCTTCATCTTCCT CAGCTTCCCAGAAATTTGGGTTATTTGGCCTAGGCTGTGCCCTGGGATTACCTCTTCATCTTCCT T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4655707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224013,Human_RBP_ID_979528,Human_RBP_ID_5856297,Human_RBP_ID_8751524,Human_RBP_ID_8973498,Human_RBP_ID_11084570,Human_RBP_ID_23409591,Human_RBP_ID_26382581 Human_miRNA_ID_574253 GWAS_ID_8216,GWAS_ID_8217 68063 RMVar_ID_68063 Human_SNP_ID_17038656 m1A Human chr1 - 67411398 67411398 67411398 GACCCATTGTTCATTGAGACAGCAACATACGCACTCCTAAATCAGTGTGTTTAGACTTTTCAAGT GACCCATTGTTCATTGAGACAGCAACATACGCGCTCCTAAATCAGTGTGTTTAGACTTTTCAAGT T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:67411347..67411448 32194978 MeRIP-seq:(Medium) rs773035057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_360967,Human_RBP_ID_979552,Human_RBP_ID_1434190,Human_RBP_ID_1752948,Human_RBP_ID_5856367,Human_RBP_ID_8049771,Human_RBP_ID_8168091,Human_RBP_ID_8751564,Human_RBP_ID_9269112,Human_RBP_ID_11084675,Human_RBP_ID_17219714,Human_RBP_ID_17336875,Human_RBP_ID_17454502,Human_RBP_ID_17756750,Human_RBP_ID_18233254,Human_RBP_ID_21878451,Human_RBP_ID_22375696,Human_RBP_ID_22785730,Human_RBP_ID_23409637,Human_RBP_ID_26590153,Human_RBP_ID_27186014,Human_RBP_ID_27597720 Human_miRNA_ID_94080 68064 RMVar_ID_68064 Human_SNP_ID_17039583 m1A Human chr1 - 67415217 67415217 67415217 GGCCGCCCAGGACGTGGCGGCAGGGGAGGACGAGGTGGACGTGGGCGTGGTGGGCGCCCAAACCG GGCCGCCCAGGACGTGGCGGCAGGGGAGGACGTGGTGGACGTGGGCGTGGTGGGCGCCCAAACCG T A SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:67415128..67415324;chr1:67415134..67415237;chr1:67415122..67415354;chr1:67415103..67415252 26863196 MeRIP-seq:(Medium) rs778722781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222100,Human_RBP_ID_361023,Human_RBP_ID_743065,Human_RBP_ID_802264,Human_RBP_ID_856641,Human_RBP_ID_979572,Human_RBP_ID_4098691,Human_RBP_ID_5856464,Human_RBP_ID_8751603,Human_RBP_ID_8973549,Human_RBP_ID_11084916,Human_RBP_ID_17756776,Human_RBP_ID_22430652,Human_RBP_ID_22488670,Human_RBP_ID_23122887,Human_RBP_ID_23409673,Human_RBP_ID_26391161,Human_RBP_ID_26868610,Human_RBP_ID_27186029,Human_RBP_ID_27400735 Human_Splice_Rec_84325,Human_Splice_Rec_84339,Human_Splice_Rec_84353,Human_Splice_Rec_84367,Human_Splice_Rec_84373 RMVar_hsa_circ_57862,RMVar_hsa_circ_118497,RMVar_hsa_circ_356432,RMVar_hsa_circ_67737,RMVar_hsa_circ_133777,RMVar_hsa_circ_54229 68065 RMVar_ID_68065 Human_SNP_ID_17040972 m1A Human chr1 + 67420082 67420082 67420082 ACTGCCCATCAGCACCTTCATTTGGTTTTCGGATATTAAATTCTACTTTTGCCCGGTCCTTATTT ACTGCCCATCAGCACCTTCATTTGGTTTTCGGGTATTAAATTCTACTTTTGCCCGGTCCTTATTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:67420051..67420150 26863196 MeRIP-seq:(Medium) rs1294753315 Functional Loss SNV dbSNP153 33..33 33 - - - 68066 RMVar_ID_68066 Human_SNP_ID_17042148 m1A Human chr1 - 67424279 67424279 67424279 AATACATTCAGAAACAAATATCTTATAATTACAGTGACTTGGATCAATCAAATGTGACTGAGGAA AATACATTCAGAAACAAATATCTTATAATTACGGTGACTTGGATCAATCAAATGTGACTGAGGAA T C SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:67424226..67424325;chr1:67424226..67424384;chr1:67424226..67424388 26863196 MeRIP-seq:(Medium) rs1407839572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_361032,Human_RBP_ID_857091,Human_RBP_ID_979575,Human_RBP_ID_1064312,Human_RBP_ID_1434228,Human_RBP_ID_1753002,Human_RBP_ID_5856578,Human_RBP_ID_8049789,Human_RBP_ID_8751609,Human_RBP_ID_8973557,Human_RBP_ID_9252426,Human_RBP_ID_9269127,Human_RBP_ID_9356448,Human_RBP_ID_11085470,Human_RBP_ID_17219746,Human_RBP_ID_17336902,Human_RBP_ID_17454535,Human_RBP_ID_17756788,Human_RBP_ID_18579961,Human_RBP_ID_19038436,Human_RBP_ID_22488673,Human_RBP_ID_22633856,Human_RBP_ID_23264058,Human_RBP_ID_23409705,Human_RBP_ID_24453770,Human_RBP_ID_26868630,Human_RBP_ID_27597761 Human_Splice_Rec_84321,Human_Splice_Rec_84334,Human_Splice_Rec_84335,Human_Splice_Rec_84349,Human_Splice_Rec_84362,Human_Splice_Rec_84363,Human_Splice_Rec_84369,Human_Splice_Rec_84381,Human_Splice_Rec_84390 Human_miRNA_ID_2247994 RMVar_hsa_circ_57862,RMVar_hsa_circ_118497,RMVar_hsa_circ_67737,RMVar_hsa_circ_24135,RMVar_hsa_circ_133777,RMVar_hsa_circ_346023,RMVar_hsa_circ_355182,RMVar_hsa_circ_333617,RMVar_hsa_circ_365704,RMVar_hsa_circ_133778 68067 RMVar_ID_68067 Human_SNP_ID_17042743 m1A Human chr1 - 67426239 67426239 67426239 GGAAGAAGACCTGATCAACAACTTCAGGGTGAAGGGAAAATAATTGATAGAAGACCAGAAAGGCG GGAAGAAGACCTGATCAACAACTTCAGGGTGAGGGGAAAATAATTGATAGAAGACCAGAAAGGCG T C SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:67426089..67426300;chr1:67426226..67426300;chr1:67426103..67426300;chr1:67425176..67429437 26863196 MeRIP-seq:(Medium) rs147465839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24952,Human_RBP_ID_224016,Human_RBP_ID_1434257,Human_RBP_ID_2183926,Human_RBP_ID_9356457,Human_RBP_ID_11085581,Human_RBP_ID_17454536,Human_RBP_ID_17756794,Human_RBP_ID_24541135,Human_RBP_ID_26309764 Human_Splice_Rec_84314,Human_Splice_Rec_84328,Human_Splice_Rec_84342,Human_Splice_Rec_84356,Human_Splice_Rec_84384 RMVar_hsa_circ_7699,RMVar_hsa_circ_57862,RMVar_hsa_circ_355182,RMVar_hsa_circ_60381 68068 RMVar_ID_68068 Human_SNP_ID_17042764 m1A Human chr1 + 67426299 67426299 67426299 CTTCCAACTCGTCTTATTCCTAAAACGATAAGATAACCTGCATAAGCAAATTATTTTTGCAATCC CTTCCAACTCGTCTTATTCCTAAAACGATAAGGTAACCTGCATAAGCAAATTATTTTTGCAATCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:67426251..67426300 26863196 MeRIP-seq:(Medium) rs1177180889 Functional Loss SNV dbSNP153 33..33 33 - - - 68069 RMVar_ID_68069 Human_SNP_ID_17043851 m1A Human chr1 - 67430086 67430086 67430086 CAACTCCAACGCGGCAGGCAAACAGCTGCGCAAGGAGTCCCAGAAAGACCGCAAGAACCCGCTGC CAACTCCAACGCGGCAGGCAAACAGCTGCGCAGGGAGTCCCAGAAAGACCGCAAGAACCCGCTGC T C SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs773507471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26800647 Human_Splice_Rec_84313,Human_Splice_Rec_84327,Human_Splice_Rec_84341,Human_Splice_Rec_84355 68070 RMVar_ID_68070 Human_SNP_ID_17043852 m1A Human chr1 - 67430086 67430086 67430086 CAACTCCAACGCGGCAGGCAAACAGCTGCGCAAGGAGTCCCAGAAAGACCGCAAGAACCCGCTGC CAACTCCAACGCGGCAGGCAAACAGCTGCGCACGGAGTCCCAGAAAGACCGCAAGAACCCGCTGC T G SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs773507471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26800647 Human_Splice_Rec_84313,Human_Splice_Rec_84327,Human_Splice_Rec_84341,Human_Splice_Rec_84355 68071 RMVar_ID_68071 Human_SNP_ID_17043854 m1A Human chr1 + 67430092 67430092 67430092 GGTTCTTGCGGTCTTTCTGGGACTCCTTGCGCAGCTGTTTGCCTGCCGCGTTGGAGTTGGTCTGG GGTTCTTGCGGTCTTTCTGGGACTCCTTGCGCTGCTGTTTGCCTGCCGCGTTGGAGTTGGTCTGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:67429954..67430415 26863410 MeRIP-seq:(Medium) rs910347320 Functional Loss SNV dbSNP153 33..33 33 - - - 68072 RMVar_ID_68072 Human_SNP_ID_17043876 m1A Human chr1 - 67430144 67430144 67430144 GCGGGGGCGGCGTTGGGGGCCCTGGGGCCAAGAGCGCAGCTCAGGCCGCGGCCCAGACCAACTCC GCGGGGGCGGCGTTGGGGGCCCTGGGGCCAAGGGCGCAGCTCAGGCCGCGGCCCAGACCAACTCC T C SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:67430076..67430150 26863196 MeRIP-seq:(Medium) rs779658689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224019,Human_RBP_ID_1434289,Human_RBP_ID_4098706,Human_RBP_ID_9318995,Human_RBP_ID_9356459,Human_RBP_ID_22025965,Human_RBP_ID_24541480,Human_RBP_ID_26309766,Human_RBP_ID_26868660,Human_RBP_ID_27186040,Human_RBP_ID_27798177 68073 RMVar_ID_68073 Human_SNP_ID_17043903 m1A Human chr1 - 67430191 67430191 67430191 CCCCTTCGAGGTGCTGAAGGCAGCAGAGAACAAGAAAAAAGAAGCCGGCGGGGGCGGCGTTGGGG CCCCTTCGAGGTGCTGAAGGCAGCAGAGAACAGGAAAAAAGAAGCCGGCGGGGGCGGCGTTGGGG T C SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:67430015..67430400 26863196 MeRIP-seq:(Medium) rs776993281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24954,Human_RBP_ID_224019,Human_RBP_ID_746009,Human_RBP_ID_1434291,Human_RBP_ID_4064308,Human_RBP_ID_8317668,Human_RBP_ID_8973564,Human_RBP_ID_9318995,Human_RBP_ID_9356460,Human_RBP_ID_9537023,Human_RBP_ID_11085810,Human_RBP_ID_17762690,Human_RBP_ID_18579977,Human_RBP_ID_22025965,Human_RBP_ID_22785779,Human_RBP_ID_22875573,Human_RBP_ID_24541480,Human_RBP_ID_24768554,Human_RBP_ID_26309767,Human_RBP_ID_26391162,Human_RBP_ID_27800437 68074 RMVar_ID_68074 Human_SNP_ID_17043932 m1A Human chr1 - 67430280 67430280 67430280 CGAGCCACCATCATGCCTGGGCACTTACAGGAAGGCTTCGGCTGCGTGGTCACCAACCGATTCGA CGAGCCACCATCATGCCTGGGCACTTACAGGAGGGCTTCGGCTGCGTGGTCACCAACCGATTCGA T C SERBP1 Ensembl:ENSG00000142864 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:67430001..67430400 26863196 MeRIP-seq:(Medium) rs1557510698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24955,Human_RBP_ID_361041,Human_RBP_ID_746009,Human_RBP_ID_800669,Human_RBP_ID_979577,Human_RBP_ID_1434293,Human_RBP_ID_1753040,Human_RBP_ID_3320700,Human_RBP_ID_4074116,Human_RBP_ID_5137573,Human_RBP_ID_5486784,Human_RBP_ID_5856680,Human_RBP_ID_8240960,Human_RBP_ID_8317671,Human_RBP_ID_8751614,Human_RBP_ID_9271459,Human_RBP_ID_9318996,Human_RBP_ID_9356463,Human_RBP_ID_17756799,Human_RBP_ID_18409944,Human_RBP_ID_18579979,Human_RBP_ID_22023478,Human_RBP_ID_23409762,Human_RBP_ID_24453786,Human_RBP_ID_26309769,Human_RBP_ID_26798538,Human_RBP_ID_26868663,Human_RBP_ID_27186041,Human_RBP_ID_27798179 68075 RMVar_ID_68075 Human_SNP_ID_17106784 m1A Human chr1 + 67685262 67685262 67685262 GCGGCCCAATTAGTGTCGTGCGGCCCGTGGCGAGGCGAGGTCCGGGGAGCGAGCGAGCAAGCAAG GCGGCCCAATTAGTGTCGTGCGGCCCGTGGCGTGGCGAGGTCCGGGGAGCGAGCGAGCAAGCAAG A T GADD45A Ensembl:ENSG00000116717 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:67685227..67685389 26863196 MeRIP-seq:(Medium) rs1378167400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742053,Human_RBP_ID_802894,Human_RBP_ID_858521,Human_RBP_ID_4074119,Human_RBP_ID_5311745,Human_RBP_ID_8939989,Human_RBP_ID_9318997,Human_RBP_ID_9412582,Human_RBP_ID_17668079,Human_RBP_ID_18414978,Human_RBP_ID_22430653,Human_RBP_ID_26311404 RMVar_hsa_circ_81465,RMVar_hsa_circ_133780 68076 RMVar_ID_68076 Human_SNP_ID_17106787 m1A Human chr1 + 67685267 67685267 67685267 CCAATTAGTGTCGTGCGGCCCGTGGCGAGGCGAGGTCCGGGGAGCGAGCGAGCAAGCAAGGCGGG CCAATTAGTGTCGTGCGGCCCGTGGCGAGGCGCGGTCCGGGGAGCGAGCGAGCAAGCAAGGCGGG A C GADD45A Ensembl:ENSG00000116717 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:67685201..67685527;chr1:67685201..67685690;chr1:67685176..67685600;chr1:67685201..67685589;chr1:67685205..67685504 26863196 MeRIP-seq:(Medium) rs1252390483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742053,Human_RBP_ID_802894,Human_RBP_ID_858521,Human_RBP_ID_4074119,Human_RBP_ID_5311745,Human_RBP_ID_8939989,Human_RBP_ID_9318997,Human_RBP_ID_9412582,Human_RBP_ID_17668079,Human_RBP_ID_18414978,Human_RBP_ID_26311404 RMVar_hsa_circ_81465,RMVar_hsa_circ_133780 68077 RMVar_ID_68077 Human_SNP_ID_17106889 m1A Human chr1 - 67685501 67685499 67685501 GGTCTTCTGCTCTCCAGCCGAGAATTCCTCCAAAGTCATATTGCAAACTGCAGGTCGCCCAGGGA GGTCTTCTGCTCTCCAGCCGAGAATTCCTCCA__GTCATATTGCAAACTGCAGGTCGCCCAGGGA CTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:67685306..67685690 32194978 MeRIP-seq:(Medium) rs750818501 Functional Loss DEL dbSNP153 33..34 33 - - - 68078 RMVar_ID_68078 Human_SNP_ID_17111282 m1A Human chr1 - 67703023 67703023 67703023 ATATGTATACATATATATGATATGCAGAAGTCACTTTTTTTATCAGGCTTTATTCTCCTTACAAA ATATGTATACATATATATGATATGCAGAAGTCCCTTTTTTTATCAGGCTTTATTCTCCTTACAAA T G GNG12 Ensembl:ENSG00000172380 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:67702973..67703068 32194978 MeRIP-seq:(Medium) rs1459893264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5856792,Human_RBP_ID_11085867,Human_RBP_ID_17219777,Human_RBP_ID_17336931,Human_RBP_ID_17454564,Human_RBP_ID_17756845,Human_RBP_ID_18233325,Human_RBP_ID_24453802,Human_RBP_ID_27597801 Human_miRNA_ID_52933,Human_miRNA_ID_60504,Human_miRNA_ID_249901,Human_miRNA_ID_383277,Human_miRNA_ID_559766,Human_miRNA_ID_567286,Human_miRNA_ID_848595,Human_miRNA_ID_1585275,Human_miRNA_ID_2375764,Human_miRNA_ID_3031409 RMVar_hsa_circ_96553,RMVar_hsa_circ_133783,RMVar_hsa_circ_75965,RMVar_hsa_circ_133782 68079 RMVar_ID_68079 Human_SNP_ID_17128343 m1A Human chr1 + 67774560 67774560 67774560 AATAGCCCTGGGCCAACCCATCAAGTCAGCAAATATCTCATTCTCCCCACCCTGGATCCTGTGTT AATAGCCCTGGGCCAACCCATCAAGTCAGCAAGTATCTCATTCTCCCCACCCTGGATCCTGTGTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:67774555..67774736 26863196 MeRIP-seq:(Medium) rs1267903032 Functional Loss SNV dbSNP153 33..33 33 - - - 68080 RMVar_ID_68080 Human_SNP_ID_17142135 m1A Human chr1 - 67832794 67832794 67832794 TTCTACCTCCCGGGACCAGCCGGCGGGAGCGCAGCCTTGGAATCCGCTGGGCGCTGGGGGTCTAG TTCTACCTCCCGGGACCAGCCGGCGGGAGCGCCGCCTTGGAATCCGCTGGGCGCTGGGGGTCTAG T G GNG12 Ensembl:ENSG00000172380 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:67832786..67832989 26863196 MeRIP-seq:(Medium) rs1351092377 Functional Loss SNV dbSNP153 33..33 33 - - - 68081 RMVar_ID_68081 Human_SNP_ID_17142153 m1A Human chr1 - 67832848 67832848 67832848 TGGAGGAGGGCTGGCATGTGGGGGCGACAGGGACGCCACGCCCCTCTGCCTACTTTCTACCTCCC TGGAGGAGGGCTGGCATGTGGGGGCGACAGGGTCGCCACGCCCCTCTGCCTACTTTCTACCTCCC T A GNG12 Ensembl:ENSG00000172380 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:67832846..67832953 26863196 MeRIP-seq:(Medium) rs1489244022 Functional Loss SNV dbSNP153 33..33 33 - - - 68082 RMVar_ID_68082 Human_SNP_ID_17142356 m1A Human chr1 - 67833387 67833387 67833387 GAGGTCGGAGCCGTCTCCAGGAGCCCTTAGAGACCGAGTCCCGGCGGCGACGGCGGGGCAGCGCA GAGGTCGGAGCCGTCTCCAGGAGCCCTTAGAGCCCGAGTCCCGGCGGCGACGGCGGGGCAGCGCA T G GNG12 Ensembl:ENSG00000172380 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:67833197..67833537 26863196 MeRIP-seq:(Medium) rs934470579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4064468 Human_Splice_Rec_84469,Human_Splice_Rec_84475 68083 RMVar_ID_68083 Human_SNP_ID_17142359 m1A Human chr1 + 67833392 67833392 67833392 TGCCCCGCCGTCGCCGCCGGGACTCGGTCTCTAAGGGCTCCTGGAGACGGCTCCGACCTCTCCTC TGCCCCGCCGTCGCCGCCGGGACTCGGTCTCTGAGGGCTCCTGGAGACGGCTCCGACCTCTCCTC A G GNG12-AS1 Ensembl:ENSG00000232284 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:67833262..67833422 26863196 MeRIP-seq:(Medium) rs1207751018 Functional Loss SNV dbSNP153 33..33 33 - - - 68084 RMVar_ID_68084 Human_SNP_ID_17146803 m1A Human chr1 + 67852762 67852762 67852762 CGGGAGAGATGAGGATGGCTTGGATCAGCGGGACAGTGGTGGAGGTGTGAGAGGTGATTATATCT CGGGAGAGATGAGGATGGCTTGGATCAGCGGGGCAGTGGTGGAGGTGTGAGAGGTGATTATATCT A G GNG12-AS1 Ensembl:ENSG00000232284 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:67852677..67852763 26863196 MeRIP-seq:(Medium) rs1247149956 Functional Loss SNV dbSNP153 33..33 33 - - - 68085 RMVar_ID_68085 Human_SNP_ID_17205092 m1A Human chr1 + 68098722 68098722 68098722 TCTTGATAAAGTTCCGAAACAAACAAAGCACAATCTTCCCTCGATTTACATGGGAGTTGCATTCC TCTTGATAAAGTTCCGAAACAAACAAAGCACAGTCTTCCCTCGATTTACATGGGAGTTGCATTCC A G GNG12-AS1 Ensembl:ENSG00000232284 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:68098621..68098721 32194978 MeRIP-seq:(Medium) rs187825885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_84482,Human_Splice_Rec_84500 RMVar_hsa_circ_2877,RMVar_hsa_circ_65276 68086 RMVar_ID_68086 Human_SNP_ID_17228740 m1A Human chr1 - 68191824 68191824 68191824 AGAGAGAAAAGCCTGGTGAGGAGGTGAGGATGAGCAAAAGAAAGAGCATTCTATATAGAAGGAAA AGAGAGAAAAGCCTGGTGAGGAGGTGAGGATGTGCAAAAGAAAGAGCATTCTATATAGAAGGAAA T A WLS Ensembl:ENSG00000116729 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:68191821..68191979 26863196 MeRIP-seq:(Medium) rs1326107399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133789,RMVar_hsa_circ_133787,RMVar_hsa_circ_338706,RMVar_hsa_circ_10694,RMVar_hsa_circ_8722 68087 RMVar_ID_68087 Human_SNP_ID_17304107 m1A Human chr1 + 68497047 68497047 68497047 CGGTGGCGTCCATGGCGGCGAAGGCGACACTCAGGCCCAGCGGCCGCGGCAGTGGCGAGTCTCGG CGGTGGCGTCCATGGCGGCGAAGGCGACACTCGGGCCCAGCGGCCGCGGCAGTGGCGAGTCTCGG A G DEPDC1-AS1 Ensembl:ENSG00000234264 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:68496963..68497051 26863196 MeRIP-seq:(Medium) rs573069288 Functional Loss SNV dbSNP153 33..33 33 - - - 68088 RMVar_ID_68088 Human_SNP_ID_17713766 m1A Human chr1 - 70189267 70189267 70189267 TCCTGGTGTGGTGCTGATGGAACTAGTGCCGCAGTGTGTCTGGAGAATAAATGTGGATATCCCTG TCCTGGTGTGGTGCTGATGGAACTAGTGCCGCCGTGTGTCTGGAGAATAAATGTGGATATCCCTG T G LRRC40 Ensembl:ENSG00000066557 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:70189220..70189320 26863196 MeRIP-seq:(Medium) rs270495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11093655,Human_RBP_ID_27835688 Human_Splice_Rec_85154 RMVar_hsa_circ_273433,RMVar_hsa_circ_334756,RMVar_hsa_circ_133860,RMVar_hsa_circ_133861,RMVar_hsa_circ_325329,RMVar_hsa_circ_360753,RMVar_hsa_circ_133865,RMVar_hsa_circ_133863,RMVar_hsa_circ_320951,RMVar_hsa_circ_345647,RMVar_hsa_circ_298865,RMVar_hsa_circ_318667,RMVar_hsa_circ_341819 68089 RMVar_ID_68089 Human_SNP_ID_17717637 m1A Human chr1 + 70205484 70205484 70205484 CCTTGGGGTACCGAGGTACCGCAGTCTCTTCCACCTGCTTTGAAACCAGCGCGGAGATCCTGCCC CCTTGGGGTACCGAGGTACCGCAGTCTCTTCCCCCTGCTTTGAAACCAGCGCGGAGATCCTGCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:70205435..70205530 26863196 MeRIP-seq:(Medium) rs958518649 Functional Loss SNV dbSNP153 33..33 33 - - - 68090 RMVar_ID_68090 Human_SNP_ID_17717664 m1A Human chr1 - 70205520 70205520 70205520 AGGACTTTGAACATGTCGCGCCTGAAGCGGATAGCGGGGCAGGATCTCCGCGCTGGTTTCAAAGC AGGACTTTGAACATGTCGCGCCTGAAGCGGATGGCGGGGCAGGATCTCCGCGCTGGTTTCAAAGC T C LRRC40 Ensembl:ENSG00000066557 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:70205436..70205533 26863196 MeRIP-seq:(Medium) rs1393396823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_361489,Human_RBP_ID_4074122,Human_RBP_ID_22871322,Human_RBP_ID_27798188 68091 RMVar_ID_68091 Human_SNP_ID_17717670 m1A Human chr1 + 70205530 70205530 70205530 CAGCGCGGAGATCCTGCCCCGCTATCCGCTTCAGGCGCGACATGTTCAAAGTCCTAGGTCCAGAA CAGCGCGGAGATCCTGCCCCGCTATCCGCTTCCGGCGCGACATGTTCAAAGTCCTAGGTCCAGAA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:70205423..70205534 26863196 MeRIP-seq:(Medium) rs771163355 Functional Loss SNV dbSNP153 33..33 33 - - - 68092 RMVar_ID_68092 Human_SNP_ID_17721689 m1A Human chr1 + 70221527 70221527 70221527 GCGGCGGCATCGGCAGCAGTAGCAGAGGCTGTAGCATCGGACACCCTCCTCTCTCCCGCAATCCG GCGGCGGCATCGGCAGCAGTAGCAGAGGCTGTGGCATCGGACACCCTCCTCTCTCCCGCAATCCG A G SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:70221476..70221800;chr1:70205731..70221754;chr1:70221370..70221650;chr1:70205731..70221735 26863196 MeRIP-seq:(Medium) rs979112776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742066,Human_RBP_ID_803307,Human_RBP_ID_1434574,Human_RBP_ID_4064774,Human_RBP_ID_11094460,Human_RBP_ID_22023485,Human_RBP_ID_22414065,Human_RBP_ID_22867648,Human_RBP_ID_24723624,Human_RBP_ID_26382854 RMVar_hsa_circ_102620,RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866,RMVar_hsa_circ_133868 68093 RMVar_ID_68093 Human_SNP_ID_17721700 m1A Human chr1 - 70221548 70221548 70221548 AGAAGGAGGGGGAAGAGGAACCGGATTGCGGGAGAGAGGAGGGTGTCCGATGCTACAGCCTCTGC AGAAGGAGGGGGAAGAGGAACCGGATTGCGGGGGAGAGGAGGGTGTCCGATGCTACAGCCTCTGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:70221463..70221650 26863196 MeRIP-seq:(Medium) rs371165024 Functional Loss SNV dbSNP153 33..33 33 - - - 68094 RMVar_ID_68094 Human_SNP_ID_17728130 m1A Human chr1 - 70246806 70246806 70246806 TTGTCTTCTTTCTTTTTGTCTCTAACAAATGAACACAATTTATGAATGCATTAGAAGACTCAGCT TTGTCTTCTTTCTTTTTGTCTCTAACAAATGACCACAATTTATGAATGCATTAGAAGACTCAGCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:70246801..70247119 32194978 MeRIP-seq:(Medium) rs1000285296 Functional Loss SNV dbSNP153 33..33 33 - - - 68095 RMVar_ID_68095 Human_SNP_ID_17729003 m1A Human chr1 + 70250473 70250473 70250473 AAGAAGAGTAAAGATAAGGAAAAGGACCGGGAAAGAAAATCAGAGAGTGATAAAGATGTAAAAGT AAGAAGAGTAAAGATAAGGAAAAGGACCGGGAGAGAAAATCAGAGAGTGATAAAGATGTAAAAGT A G SRSF11 Ensembl:ENSG00000116754 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:70250340..70250758 26863196 MeRIP-seq:(Medium) rs757016269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24354,Human_RBP_ID_223708,Human_RBP_ID_854856,Human_RBP_ID_1438160,Human_RBP_ID_1753513,Human_RBP_ID_2183989,Human_RBP_ID_3933633,Human_RBP_ID_5519065,Human_RBP_ID_5538024,Human_RBP_ID_5860168,Human_RBP_ID_8228018,Human_RBP_ID_8974059,Human_RBP_ID_9356478,Human_RBP_ID_11095863,Human_RBP_ID_17646462,Human_RBP_ID_18410181,Human_RBP_ID_22350482,Human_RBP_ID_22871808,Human_RBP_ID_23112426,Human_RBP_ID_23410942,Human_RBP_ID_24541153,Human_RBP_ID_24550371,Human_RBP_ID_26311431 Human_Splice_Rec_85203,Human_Splice_Rec_85231,Human_Splice_Rec_85315,Human_Splice_Rec_85333,Human_Splice_Rec_85347,Human_Splice_Rec_85353,Human_Splice_Rec_85355,Human_Splice_Rec_85359 RMVar_hsa_circ_56822,RMVar_hsa_circ_57402,RMVar_hsa_circ_316622,RMVar_hsa_circ_363422 68096 RMVar_ID_68096 Human_SNP_ID_17729168 m1A Human chr1 + 70251059 70251059 70251059 ACCAAGCAGTTTTACTATTCTGGTGCTGCTTCATAACAAAAATGAAAAGCTGCATGCATCTACAG ACCAAGCAGTTTTACTATTCTGGTGCTGCTTCGTAACAAAAATGAAAAGCTGCATGCATCTACAG A G SRSF11 Ensembl:ENSG00000116754 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:70251008..70251108 32194978 MeRIP-seq:(Medium) rs536139755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_361550,Human_RBP_ID_1434652,Human_RBP_ID_1753516,Human_RBP_ID_8318271,Human_RBP_ID_8751714,Human_RBP_ID_8974066,Human_RBP_ID_9356484,Human_RBP_ID_11095886,Human_RBP_ID_17219881,Human_RBP_ID_18158326,Human_RBP_ID_18233516,Human_RBP_ID_18584433,Human_RBP_ID_22735580,Human_RBP_ID_23410957,Human_RBP_ID_26798540,Human_RBP_ID_26869045,Human_RBP_ID_27598074 Human_miRNA_ID_833945 68097 RMVar_ID_68097 Human_SNP_ID_17729296 m1A Human chr1 + 70251657 70251657 70251657 ACCTTATCTCTTGCCCTTATTTTGAATTTTCCACTCTTTCATTAATTTGTTTTAAGCTCCGTGTT ACCTTATCTCTTGCCCTTATTTTGAATTTTCCGCTCTTTCATTAATTTGTTTTAAGCTCCGTGTT A G SRSF11 Ensembl:ENSG00000116754 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:70251606..70251706 32194978 MeRIP-seq:(Medium) rs1423760139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_361583,Human_RBP_ID_1257323,Human_RBP_ID_5860200,Human_RBP_ID_8318276,Human_RBP_ID_11095922,Human_RBP_ID_17337031,Human_RBP_ID_17757318,Human_RBP_ID_18233530,Human_RBP_ID_18580438,Human_RBP_ID_22376874,Human_RBP_ID_22488705,Human_RBP_ID_22785904,Human_RBP_ID_22875667,Human_RBP_ID_24453986,Human_RBP_ID_24768858,Human_RBP_ID_26869057,Human_RBP_ID_27598093 68098 RMVar_ID_68098 Human_SNP_ID_17754179 m1A Human chr1 + 70354482 70354482 70354482 GCTGGCGACGGAGCTGGCGCTGCGGCGGCACAAGGCGATTAGAGCGGTGGCCAAGAGCCTCCAGC GCTGGCGACGGAGCTGGCGCTGCGGCGGCACACGGCGATTAGAGCGGTGGCCAAGAGCCTCCAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:70354383..70354484 26863196 MeRIP-seq:(Medium) rs887201010 Functional Loss SNV dbSNP153 33..33 33 - - - 68099 RMVar_ID_68099 Human_SNP_ID_17754180 m1A Human chr1 + 70354482 70354482 70354482 GCTGGCGACGGAGCTGGCGCTGCGGCGGCACAAGGCGATTAGAGCGGTGGCCAAGAGCCTCCAGC GCTGGCGACGGAGCTGGCGCTGCGGCGGCACAGGGCGATTAGAGCGGTGGCCAAGAGCCTCCAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:70354383..70354484 26863196 MeRIP-seq:(Medium) rs887201010 Functional Loss SNV dbSNP153 33..33 33 - - - 68100 RMVar_ID_68100 Human_SNP_ID_17754204 m1A Human chr1 + 70354595 70354595 70354595 CCGGGGAAGAGCCGGCTCTCGCCTAGGCACGAAGGGACGCGCGCTCGCTGGGGGAAGCTAGAACT CCGGGGAAGAGCCGGCTCTCGCCTAGGCACGACGGGACGCGCGCTCGCTGGGGGAAGCTAGAACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:70354546..70354684 26863196 MeRIP-seq:(Medium) rs561736987 Functional Loss SNV dbSNP153 33..33 33 - - - 68101 RMVar_ID_68101 Human_SNP_ID_17754224 m1A Human chr1 + 70354667 70354667 70354667 CCACGACACCAGGATCTCAGTCTCGCCGTCGCAGCCGCCGTCGCTGCCTTACACCGAAAAACAGG CCACGACACCAGGATCTCAGTCTCGCCGTCGCGGCCGCCGTCGCTGCCTTACACCGAAAAACAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:70354580..70354674 26863196 MeRIP-seq:(Medium) rs1275818987 Functional Loss SNV dbSNP153 33..33 33 - - - 68102 RMVar_ID_68102 Human_SNP_ID_17754323 m1A Human chr1 - 70354899 70354899 70354899 TCCGACCGCCCACAAAAAGCGCGGTTGGCGGGAGTGCGGGTTCGGGGTCGGCTGGCAGCTGGGAG TCCGACCGCCCACAAAAAGCGCGGTTGGCGGGGGTGCGGGTTCGGGGTCGGCTGGCAGCTGGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:70354853..70355030 26863196 MeRIP-seq:(Medium) rs1045833880 Functional Loss SNV dbSNP153 33..33 33 - - - 68103 RMVar_ID_68103 Human_SNP_ID_17754334 m1A Human chr1 - 70354927 70354927 70354927 CCGAACATATCCAACGGAGGCTGTGGTTTCCGACCGCCCACAAAAAGCGCGGTTGGCGGGAGTGC CCGAACATATCCAACGGAGGCTGTGGTTTCCGGCCGCCCACAAAAAGCGCGGTTGGCGGGAGTGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:70354826..70355025 26863410 MeRIP-seq:(Medium) rs781063774 Functional Loss SNV dbSNP153 33..33 33 - - - 68104 RMVar_ID_68104 Human_SNP_ID_17754335 m1A Human chr1 - 70354927 70354927 70354927 CCGAACATATCCAACGGAGGCTGTGGTTTCCGACCGCCCACAAAAAGCGCGGTTGGCGGGAGTGC CCGAACATATCCAACGGAGGCTGTGGTTTCCGCCCGCCCACAAAAAGCGCGGTTGGCGGGAGTGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:70354826..70355025 26863410 MeRIP-seq:(Medium) rs781063774 Functional Loss SNV dbSNP153 33..33 33 - - - 68105 RMVar_ID_68105 Human_SNP_ID_17767283 m1A Human chr1 - 70411316 70411314 70411317 GGGGTTGGGAGAGACAGAAGGATCAGGCGAGAAGGAGCTAAAGCACGCAGGTAGAGCCGACGGCG GGGGTTGGGAGAGACAGAAGGATCAGGCGAG___GAGCTAAAGCACGCAGGTAGAGCCGACGGCG CCTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:70411276..70411513;chr1:70411271..70411430 26863196 MeRIP-seq:(Medium) rs903475887 Functional Loss DEL dbSNP153 32..34 33 - - - 68106 RMVar_ID_68106 Human_SNP_ID_17767284 m1A Human chr1 - 70411316 70411316 70411316 GGGGTTGGGAGAGACAGAAGGATCAGGCGAGAAGGAGCTAAAGCACGCAGGTAGAGCCGACGGCG GGGGTTGGGAGAGACAGAAGGATCAGGCGAGAGGGAGCTAAAGCACGCAGGTAGAGCCGACGGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:70411276..70411513;chr1:70411271..70411430 26863196 MeRIP-seq:(Medium) rs912398497 Functional Loss SNV dbSNP153 33..33 33 - - - 68107 RMVar_ID_68107 Human_SNP_ID_17930368 m1A Human chr1 - 71080871 71080871 71080871 TGTTAGTGGAAGCTTTCCGAGGTCCGTCCGGCATTTTCCTTTTTTATGATTTTCTGTGCCTTAAG TGTTAGTGGAAGCTTTCCGAGGTCCGTCCGGCGTTTTCCTTTTTTATGATTTTCTGTGCCTTAAG T C ZRANB2 Ensembl:ENSG00000132485 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:71080870..71081025 26863410 MeRIP-seq:(Medium) rs768204927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11100416,Human_RBP_ID_22469397 RMVar_hsa_circ_82783,RMVar_hsa_circ_133922,RMVar_hsa_circ_133928,RMVar_hsa_circ_124017 68108 RMVar_ID_68108 Human_SNP_ID_17930396 m1A Human chr1 + 71080923 71080923 71080923 GCTTCCACTAACAAACTCCGTCCCAATTCAGGACCCTTCTTGAACTCACTTTTTGTCAGGGCAAA GCTTCCACTAACAAACTCCGTCCCAATTCAGGCCCCTTCTTGAACTCACTTTTTGTCAGGGCAAA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:71080919..71081025 26863410 MeRIP-seq:(Medium) rs759313363 Functional Loss SNV dbSNP153 33..33 33 - - - 68109 RMVar_ID_68109 Human_SNP_ID_17930397 m1A Human chr1 + 71080923 71080923 71080923 GCTTCCACTAACAAACTCCGTCCCAATTCAGGACCCTTCTTGAACTCACTTTTTGTCAGGGCAAA GCTTCCACTAACAAACTCCGTCCCAATTCAGGGCCCTTCTTGAACTCACTTTTTGTCAGGGCAAA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:71080919..71081025 26863410 MeRIP-seq:(Medium) rs759313363 Functional Loss SNV dbSNP153 33..33 33 - - - 68110 RMVar_ID_68110 Human_SNP_ID_17930410 m1A Human chr1 + 71080981 71080981 71080981 GGGCAAATCCAGTCCCCGTCACTGACTCGGAAATTCTTGGTCGACATCTTGAACGCCACCAGCAC GGGCAAATCCAGTCCCCGTCACTGACTCGGAAGTTCTTGGTCGACATCTTGAACGCCACCAGCAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:71080951..71081025 26863196 MeRIP-seq:(Medium) rs1464207637 Functional Loss SNV dbSNP153 33..33 33 - - - 68111 RMVar_ID_68111 Human_SNP_ID_17930411 m1A Human chr1 - 71080982 71080982 71080982 TGTGCTGGTGGCGTTCAAGATGTCGACCAAGAATTTCCGAGTCAGTGACGGGGACTGGATTTGCC TGTGCTGGTGGCGTTCAAGATGTCGACCAAGAGTTTCCGAGTCAGTGACGGGGACTGGATTTGCC T C ZRANB2 Ensembl:ENSG00000132485 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:71070890..71081025 26863196 MeRIP-seq:(Medium) rs376338886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19778,Human_RBP_ID_742714,Human_RBP_ID_979753,Human_RBP_ID_1434892,Human_RBP_ID_1753692,Human_RBP_ID_2164143,Human_RBP_ID_3321399,Human_RBP_ID_4074127,Human_RBP_ID_5861779,Human_RBP_ID_11100422,Human_RBP_ID_23411527,Human_RBP_ID_24541163,Human_RBP_ID_26311453,Human_RBP_ID_26869227,Human_RBP_ID_27798219 Human_Splice_Rec_85643,Human_Splice_Rec_85663,Human_Splice_Rec_85693 RMVar_hsa_circ_82783,RMVar_hsa_circ_133922,RMVar_hsa_circ_133928,RMVar_hsa_circ_124017 68112 RMVar_ID_68112 Human_SNP_ID_17930412 m1A Human chr1 - 71080982 71080982 71080982 TGTGCTGGTGGCGTTCAAGATGTCGACCAAGAATTTCCGAGTCAGTGACGGGGACTGGATTTGCC TGTGCTGGTGGCGTTCAAGATGTCGACCAAGACTTTCCGAGTCAGTGACGGGGACTGGATTTGCC T G ZRANB2 Ensembl:ENSG00000132485 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:71070890..71081025 26863196 MeRIP-seq:(Medium) rs376338886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19778,Human_RBP_ID_742714,Human_RBP_ID_979753,Human_RBP_ID_1434892,Human_RBP_ID_1753692,Human_RBP_ID_2164143,Human_RBP_ID_3321399,Human_RBP_ID_4074127,Human_RBP_ID_5861779,Human_RBP_ID_11100422,Human_RBP_ID_23411527,Human_RBP_ID_24541163,Human_RBP_ID_26311453,Human_RBP_ID_26869227,Human_RBP_ID_27798219 Human_Splice_Rec_85643,Human_Splice_Rec_85663,Human_Splice_Rec_85693 RMVar_hsa_circ_82783,RMVar_hsa_circ_133922,RMVar_hsa_circ_133928,RMVar_hsa_circ_124017 68113 RMVar_ID_68113 Human_SNP_ID_17930416 m1A Human chr1 - 71080989 71080989 71080989 GGGTGGCTGTGCTGGTGGCGTTCAAGATGTCGACCAAGAATTTCCGAGTCAGTGACGGGGACTGG GGGTGGCTGTGCTGGTGGCGTTCAAGATGTCGGCCAAGAATTTCCGAGTCAGTGACGGGGACTGG T C ZRANB2 Ensembl:ENSG00000132485 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:71080880..71081050;chr1:71080874..71081005;chr1:71080863..71081025;chr1:71080885..71081025;chr1:71072101..71081025 26863196 MeRIP-seq:(Medium) rs750478048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19778,Human_RBP_ID_742714,Human_RBP_ID_979753,Human_RBP_ID_1434892,Human_RBP_ID_1753692,Human_RBP_ID_3321399,Human_RBP_ID_4074127,Human_RBP_ID_5108664,Human_RBP_ID_8974239,Human_RBP_ID_11100422,Human_RBP_ID_24541163,Human_RBP_ID_26311453,Human_RBP_ID_26869227,Human_RBP_ID_27798219 Human_Splice_Rec_85643,Human_Splice_Rec_85663,Human_Splice_Rec_85693 RMVar_hsa_circ_82783,RMVar_hsa_circ_133922,RMVar_hsa_circ_133928,RMVar_hsa_circ_124017 68114 RMVar_ID_68114 Human_SNP_ID_18122083 m1A Human chr1 + 71868745 71868745 71868745 ATTTCTGAAACACACTTCTACTCCTTCCTCTCACTTATGTCTGCACTTTATATTCCTTCTTTCCT ATTTCTGAAACACACTTCTACTCCTTCCTCTCGCTTATGTCTGCACTTTATATTCCTTCTTTCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:71868732..71868818 26863196 MeRIP-seq:(Medium) rs902095330 Functional Loss SNV dbSNP153 33..33 33 - - - 68115 RMVar_ID_68115 Human_SNP_ID_18226388 m1A Human chr1 + 72282415 72282415 72282415 CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCAGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCCGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:72282367..72282724 26863196 MeRIP-seq:(Medium) rs1248610517 Functional Loss SNV dbSNP153 33..33 33 - - - 68116 RMVar_ID_68116 Human_SNP_ID_18834003 m1A Human chr1 - 74732995 74732995 74732995 AGGTGTGGCAGTCCTCATTTCTGTGGAATCTGAAGAAGCCCACGCAGATTTTAATTCCCACTCTA AGGTGTGGCAGTCCTCATTTCTGTGGAATCTGCAGAAGCCCACGCAGATTTTAATTCCCACTCTA T G CRYZ Ensembl:ENSG00000116791 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:74732958..74733112 26863196 MeRIP-seq:(Medium) rs1328955018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1434932,Human_RBP_ID_4065158,Human_RBP_ID_19035014,Human_RBP_ID_22430672 Human_Splice_Rec_86925,Human_Splice_Rec_86937,Human_Splice_Rec_86955,Human_Splice_Rec_86973,Human_Splice_Rec_86987 68117 RMVar_ID_68117 Human_SNP_ID_18834107 m1A Human chr1 + 74733225 74733225 74733225 AGAGACGAGGCTACCATGAAGGAGCCGAGCGCAGACCCTGAGTCCGTCACCCATGGATCGCAGCG AGAGACGAGGCTACCATGAAGGAGCCGAGCGCCGACCCTGAGTCCGTCACCCATGGATCGCAGCG A C TYW3 Ensembl:ENSG00000162623 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:74733174..74733312 26863196 MeRIP-seq:(Medium) rs769744230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5862577,Human_RBP_ID_11101492,Human_RBP_ID_18414983,Human_RBP_ID_18580700 68118 RMVar_ID_68118 Human_SNP_ID_18834108 m1A Human chr1 + 74733227 74733227 74733227 AGACGAGGCTACCATGAAGGAGCCGAGCGCAGACCCTGAGTCCGTCACCCATGGATCGCAGCGCG AGACGAGGCTACCATGAAGGAGCCGAGCGCAGCCCCTGAGTCCGTCACCCATGGATCGCAGCGCG A C TYW3 Ensembl:ENSG00000162623 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:74733176..74733350;chr1:74733176..74733302 26863196 MeRIP-seq:(Medium) rs1375200548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5862577,Human_RBP_ID_11101492,Human_RBP_ID_18414983,Human_RBP_ID_18580700 68119 RMVar_ID_68119 Human_SNP_ID_737289901 m1A Human chrY - 11160286 11160286 11160286 CTGTGGTGGGAGAGGAGGTGAAGGTGGAAGGAACAGGGGCCCAGGGGCCTGTGCTGTAGGAAGGG CTGTGGTGGGAGAGGAGGTGAAGGTGGAAGGAGCAGGGGCCCAGGGGCCTGTGCTGTAGGAAGGG T C AC134878.2 Ensembl:ENSG00000278212 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrY:11160234..11160323 26863196 MeRIP-seq:(Medium) rs75686528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27152582 68120 RMVar_ID_68120 Human_SNP_ID_737303712 m1A Human chrY - 11294468 11294468 11294468 GAGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATAGAATGGGATGGGATGGGGTG GAGTGGAATGGAATGGAATGGAATGGAATGGAGTGGAATGGAATAGAATGGGATGGGATGGGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11294447..11294532 26863196 MeRIP-seq:(Medium) rs377619153 Functional Loss SNV dbSNP153 33..33 33 - - - 68121 RMVar_ID_68121 Human_SNP_ID_737304921 m1A Human chrY + 11297768 11297768 11297768 TCTATTTCATGCCATTCCACTCGGGTTGATTCAATTCCATTGTATTCCATTCCATTCCATTCCAT TCTATTTCATGCCATTCCACTCGGGTTGATTCCATTCCATTGTATTCCATTCCATTCCATTCCAT A C RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11297495..11297842 26863196 MeRIP-seq:(Medium) rs368910641 Functional Loss SNV dbSNP153 33..33 33 - - - 68122 RMVar_ID_68122 Human_SNP_ID_737305301 m1A Human chrY + 11298862 11298862 11298862 CCATTCAATTTCATGCGATTACACTCGGGTTGATTCCATTCCATTCCATTCCATTCCTTTCCATT CCATTCAATTTCATGCGATTACACTCGGGTTGTTTCCATTCCATTCCATTCCATTCCTTTCCATT A T RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11298847..11298934 26863196 MeRIP-seq:(Medium) rs1029315357 Functional Loss SNV dbSNP153 33..33 33 - - - 68123 RMVar_ID_68123 Human_SNP_ID_737305764 m1A Human chrY + 11300234 11300234 11300234 CCATTCTATTCCATTCAATTTCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCATTCTATTCCATTCAATTTCATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATT A T RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11300213..11300428 26863196 MeRIP-seq:(Medium) rs74220552 Functional Loss SNV dbSNP153 33..33 33 - - - 68124 RMVar_ID_68124 Human_SNP_ID_737306615 m1A Human chrY + 11302762 11302762 11302762 CATTCCATTCCCTTCCATTCCATTCCACTCGGAATGATTCCATTCCATTCCATTCCATTCCATTC CATTCCATTCCCTTCCATTCCATTCCACTCGGGATGATTCCATTCCATTCCATTCCATTCCATTC A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11302724..11302836 26863196 MeRIP-seq:(Medium) rs916792990 Functional Loss SNV dbSNP153 33..33 33 - - - 68125 RMVar_ID_68125 Human_SNP_ID_737306616 m1A Human chrY + 11302762 11302762 11302762 CATTCCATTCCCTTCCATTCCATTCCACTCGGAATGATTCCATTCCATTCCATTCCATTCCATTC CATTCCATTCCCTTCCATTCCATTCCACTCGGTATGATTCCATTCCATTCCATTCCATTCCATTC A T RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11302724..11302836 26863196 MeRIP-seq:(Medium) rs916792990 Functional Loss SNV dbSNP153 33..33 33 - - - 68126 RMVar_ID_68126 Human_SNP_ID_737606238 m1A Human chrY + 26638321 26638321 26638321 GAATGGAGTGGAGTGGAATGGAGTGGAATGGAATGGAATGCAATGGAGTGGAATGGAAAGGAATG GAATGGAGTGGAGTGGAATGGAGTGGAATGGAGTGGAATGCAATGGAGTGGAATGGAAAGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:26638202..26638356 26863196 MeRIP-seq:(Medium) rs926690920 Functional Loss SNV dbSNP153 33..33 33 - - - 68127 RMVar_ID_68127 Human_SNP_ID_737606239 m1A Human chrY + 26638321 26638321 26638321 GAATGGAGTGGAGTGGAATGGAGTGGAATGGAATGGAATGCAATGGAGTGGAATGGAAAGGAATG GAATGGAGTGGAGTGGAATGGAGTGGAATGGATTGGAATGCAATGGAGTGGAATGGAAAGGAATG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:26638202..26638356 26863196 MeRIP-seq:(Medium) rs926690920 Functional Loss SNV dbSNP153 33..33 33 - - - 68128 RMVar_ID_68128 Human_SNP_ID_737629115 m1A Human chrY - 56834420 56834420 56834420 GAAGGGAATGGAATGGAGTGGAATGGAATGAAATGGAATGGAGTGGAGTGGAGAGGAGTGGAATG GAAGGGAATGGAATGGAGTGGAATGGAATGAAGTGGAATGGAGTGGAGTGGAGAGGAGTGGAATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:56834369..56834518 26863196 MeRIP-seq:(Medium) rs368333968 Functional Loss SNV dbSNP153 33..33 33 - - - 68129 RMVar_ID_68129 Human_SNP_ID_449437395 m1A Human chr10 + 120979771 120979771 120979771 CGGGTGCAGCCGGCGCGGTCCCACGTGTCCCTACCGCGAGCCGCTCCCCGCGTCCCTGCTGCCGC CGGGTGCAGCCGGCGCGGTCCCACGTGTCCCTGCCGCGAGCCGCTCCCCGCGTCCCTGCTGCCGC A G lnc-WDR11-3 RNACentral:URS00008B363C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:120979722..120979787 26863196 MeRIP-seq:(Medium) rs941765580 Functional Loss SNV dbSNP153 33..33 33 - - - 68130 RMVar_ID_68130 Human_SNP_ID_449624345 m1A Human chr10 - 121742495 121742495 121742495 AGTCGAGCTGTCTGGGAAACAGGATGAAAAACAGGAGGGTTATTTTCTTGTGCCCTCTTTGTCAG AGTCGAGCTGTCTGGGAAACAGGATGAAAAACGGGAGGGTTATTTTCTTGTGCCCTCTTTGTCAG T C ATE1 Ensembl:ENSG00000107669 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:121742470..121742580 32194978 MeRIP-seq:(Medium) rs1222392826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_372509,Human_RBP_ID_17771647 68131 RMVar_ID_68131 Human_SNP_ID_449646317 m1A Human chr10 - 121836151 121836151 121836151 AAGATGTGGAAGAGGAAAGGAAGGAGTAGCTCAAGAAGAAAGTAGGTAGGATGGAGAAGGACGTT AAGATGTGGAAGAGGAAAGGAAGGAGTAGCTCCAGAAGAAAGTAGGTAGGATGGAGAAGGACGTT T G ATE1 Ensembl:ENSG00000107669 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:121836032..121836165 26863196 MeRIP-seq:(Medium) rs962354423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146819,RMVar_hsa_circ_278012,RMVar_hsa_circ_289965,RMVar_hsa_circ_322912,RMVar_hsa_circ_340338,RMVar_hsa_circ_347181,RMVar_hsa_circ_335376,RMVar_hsa_circ_309481,RMVar_hsa_circ_279098,RMVar_hsa_circ_146823,RMVar_hsa_circ_114436,RMVar_hsa_circ_276678,RMVar_hsa_circ_146824,RMVar_hsa_circ_146821,RMVar_hsa_circ_146822,RMVar_hsa_circ_146820,RMVar_hsa_circ_146825 68132 RMVar_ID_68132 Human_SNP_ID_449669760 m1A Human chr10 + 121928249 121928249 121928249 AGGGAAACAGGATGGGGAGAGTCAAGAGGGGAAGGGAAGCGGGAGTCGGGGTGCGAGCCTGCCCT AGGGAAACAGGATGGGGAGAGTCAAGAGGGGAGGGGAAGCGGGAGTCGGGGTGCGAGCCTGCCCT A G ATE1-AS1,ATE1-AS1:2 RNACentral:URS00008BBC08,RNACentral:URS00008B78E2 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:121924307..121928453 26863196 MeRIP-seq:(Medium) rs1248307409 Functional Loss SNV dbSNP153 33..33 33 - - - 68133 RMVar_ID_68133 Human_SNP_ID_449681558 m1A Human chr10 + 121974693 121974693 121974693 GACCCGCGCCAAGGTCGTACGGCTCCAGCCACAAAGTGGGAGCACTTTGTCAACAATTTAAGGTG GACCCGCGCCAAGGTCGTACGGCTCCAGCCACGAAGTGGGAGCACTTTGTCAACAATTTAAGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:121974687..121974775 26863196 MeRIP-seq:(Medium) rs1216195428 Functional Loss SNV dbSNP153 33..33 33 - - - 68134 RMVar_ID_68134 Human_SNP_ID_449681749 m1A Human chr10 - 121975134 121975134 121975134 TATGTCTGGGGACAGCAGCGGCCGCGGGCCAGAGGGCCGGGGCCGGGGCCGCGACCCGCATCGGG TATGTCTGGGGACAGCAGCGGCCGCGGGCCAGGGGGCCGGGGCCGGGGCCGCGACCCGCATCGGG T C NSMCE4A Ensembl:ENSG00000107672 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr10:121975051..121975200;chr10:121975065..121975147 26863410 MeRIP-seq:(Medium) rs1428963926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225712,Human_RBP_ID_4136545,Human_RBP_ID_9360912,Human_RBP_ID_18970456,Human_RBP_ID_26754172 68135 RMVar_ID_68135 Human_SNP_ID_449698225 m1A Human chr10 + 122039399 122039399 122039399 GGGCAGCTGGCATGGGTAAGGTGGGAAGGTTAAGGGTCTGTTCCGTGATGATCCTGGGATATGAG GGGCAGCTGGCATGGGTAAGGTGGGAAGGTTAGGGGTCTGTTCCGTGATGATCCTGGGATATGAG A G TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:122039396..122039591 26863196 MeRIP-seq:(Medium) rs1350093076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11289003 RMVar_hsa_circ_64940 68136 RMVar_ID_68136 Human_SNP_ID_449702355 m1A Human chr10 + 122055239 122055239 122055239 AAGACGCCGTCTCCCAAAAAAAAATAAAAAAAAAGTGAAGAAGGGTGACGTGAACAAGCATGAGG AAGACGCCGTCTCCCAAAAAAAAATAAAAAAACAGTGAAGAAGGGTGACGTGAACAAGCATGAGG A C TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:122055224..122055313 26863196 MeRIP-seq:(Medium) rs1214453096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72213 68137 RMVar_ID_68137 Human_SNP_ID_449711195 m1A Human chr10 + 122086526 122086525 122086526 ATGCCACTTCTGGCCAAGGGCAAGCAGGCAACAGGGGAAGAGAAAGCAGCAACAGCTCCAGGTGC ATGCCACTTCTGGCCAAGGGCAAGCAGGCAAC_GGGGAAGAGAAAGCAGCAACAGCTCCAGGTGC CA C TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:122086501..122086575 26863196 MeRIP-seq:(Medium) rs1325271548 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_72213,RMVar_hsa_circ_354691 68138 RMVar_ID_68138 Human_SNP_ID_449711203 m1A Human chr10 + 122086547 122086547 122086547 AAGCAGGCAACAGGGGAAGAGAAAGCAGCAACAGCTCCAGGTGCAGGTGCCAAGGCCAGTGGGGA AAGCAGGCAACAGGGGAAGAGAAAGCAGCAACGGCTCCAGGTGCAGGTGCCAAGGCCAGTGGGGA A G TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:122086501..122086656 26863196 MeRIP-seq:(Medium) rs756815559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72213,RMVar_hsa_circ_354691 68139 RMVar_ID_68139 Human_SNP_ID_449711213 m1A Human chr10 - 122086585 122086585 122086585 TGCCCTCTGTCTCTCCTGCTGCATCACCTGCCATGCCCTCCCCACTGGCCTTGGCACCTGCACCT TGCCCTCTGTCTCTCCTGCTGCATCACCTGCCCTGCCCTCCCCACTGGCCTTGGCACCTGCACCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122086536..122086689 26863196 MeRIP-seq:(Medium) rs2420986 Functional Loss SNV dbSNP153 33..33 33 - - - 68140 RMVar_ID_68140 Human_SNP_ID_449714004 m1A Human chr10 + 122097400 122097391 122097401 GTTGGAGGAGGAGAAGGAGGAGAAAAGAAGAAAGAAGAAGAAACTCAGGGGAAGGGAGTCTATGT GTTGGAGGAGGAGAAGGAGGAGAA__________AAGAAGAAACTCAGGGGAAGGGAGTCTATGT AAAGAAGAAAG A TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122097303..122097638 26863196 MeRIP-seq:(Medium) rs1482831477 Functional Loss DEL dbSNP153 25..34 33 - - - 68141 RMVar_ID_68141 Human_SNP_ID_449714005 m1A Human chr10 + 122097400 122097398 122097401 GTTGGAGGAGGAGAAGGAGGAGAAAAGAAGAAAGAAGAAGAAACTCAGGGGAAGGGAGTCTATGT GTTGGAGGAGGAGAAGGAGGAGAAAAGAAGA___AAGAAGAAACTCAGGGGAAGGGAGTCTATGT AAAG A TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122097303..122097638 26863196 MeRIP-seq:(Medium) rs1254138924 Functional Loss DEL dbSNP153 32..34 33 - - - 68142 RMVar_ID_68142 Human_SNP_ID_449739014 m1A Human chr10 + 122195118 122195114 122195118 CCTGTCAAAGCTCCGCCAGCTCCACCCCCACCACCCCCCGAAGTCATCCCAGAACCCGAGGTCAG CCTGTCAAAGCTCCGCCAGCTCCACCCCC____CCCCCCGAAGTCATCCCAGAACCCGAGGTCAG CACCA C TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:122195069..122195165 26863196 MeRIP-seq:(Medium) rs1318215449 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_864363 Human_Splice_Rec_1183498,Human_Splice_Rec_1183499,Human_Splice_Rec_1183540,Human_Splice_Rec_1183541,Human_Splice_Rec_1183582,Human_Splice_Rec_1183583,Human_Splice_Rec_1183620,Human_Splice_Rec_1183621,Human_Splice_Rec_1183668,Human_Splice_Rec_1183669,Human_Splice_Rec_1183704,Human_Splice_Rec_1183705,Human_Splice_Rec_1183744,Human_Splice_Rec_1183745,Human_Splice_Rec_1183778,Human_Splice_Rec_1183779,Human_Splice_Rec_1183784,Human_Splice_Rec_1183785,Human_Splice_Rec_1183813,Human_Splice_Rec_1183818,Human_Splice_Rec_1183819,Human_Splice_Rec_1183846,Human_Splice_Rec_1183847,Human_Splice_Rec_1183876,Human_Splice_Rec_1183877,Human_Splice_Rec_1183910,Human_Splice_Rec_1183911,Human_Splice_Rec_1183942,Human_Splice_Rec_1183943,Human_Splice_Rec_1183973 RMVar_hsa_circ_146860,RMVar_hsa_circ_124449 68143 RMVar_ID_68143 Human_SNP_ID_449739019 m1A Human chr10 + 122195118 122195118 122195118 CCTGTCAAAGCTCCGCCAGCTCCACCCCCACCACCCCCCGAAGTCATCCCAGAACCCGAGGTCAG CCTGTCAAAGCTCCGCCAGCTCCACCCCCACCCCCCCCCGAAGTCATCCCAGAACCCGAGGTCAG A C TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:122195069..122195165 26863196 MeRIP-seq:(Medium) rs748566906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864363 Human_Splice_Rec_1183498,Human_Splice_Rec_1183499,Human_Splice_Rec_1183540,Human_Splice_Rec_1183541,Human_Splice_Rec_1183582,Human_Splice_Rec_1183583,Human_Splice_Rec_1183620,Human_Splice_Rec_1183621,Human_Splice_Rec_1183668,Human_Splice_Rec_1183669,Human_Splice_Rec_1183704,Human_Splice_Rec_1183705,Human_Splice_Rec_1183744,Human_Splice_Rec_1183745,Human_Splice_Rec_1183778,Human_Splice_Rec_1183779,Human_Splice_Rec_1183784,Human_Splice_Rec_1183785,Human_Splice_Rec_1183813,Human_Splice_Rec_1183818,Human_Splice_Rec_1183819,Human_Splice_Rec_1183846,Human_Splice_Rec_1183847,Human_Splice_Rec_1183876,Human_Splice_Rec_1183877,Human_Splice_Rec_1183910,Human_Splice_Rec_1183911,Human_Splice_Rec_1183942,Human_Splice_Rec_1183943,Human_Splice_Rec_1183973 RMVar_hsa_circ_146860,RMVar_hsa_circ_124449 68144 RMVar_ID_68144 Human_SNP_ID_449739020 m1A Human chr10 + 122195118 122195118 122195118 CCTGTCAAAGCTCCGCCAGCTCCACCCCCACCACCCCCCGAAGTCATCCCAGAACCCGAGGTCAG CCTGTCAAAGCTCCGCCAGCTCCACCCCCACCGCCCCCCGAAGTCATCCCAGAACCCGAGGTCAG A G TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:122195069..122195165 26863196 MeRIP-seq:(Medium) rs748566906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864363 Human_Splice_Rec_1183498,Human_Splice_Rec_1183499,Human_Splice_Rec_1183540,Human_Splice_Rec_1183541,Human_Splice_Rec_1183582,Human_Splice_Rec_1183583,Human_Splice_Rec_1183620,Human_Splice_Rec_1183621,Human_Splice_Rec_1183668,Human_Splice_Rec_1183669,Human_Splice_Rec_1183704,Human_Splice_Rec_1183705,Human_Splice_Rec_1183744,Human_Splice_Rec_1183745,Human_Splice_Rec_1183778,Human_Splice_Rec_1183779,Human_Splice_Rec_1183784,Human_Splice_Rec_1183785,Human_Splice_Rec_1183813,Human_Splice_Rec_1183818,Human_Splice_Rec_1183819,Human_Splice_Rec_1183846,Human_Splice_Rec_1183847,Human_Splice_Rec_1183876,Human_Splice_Rec_1183877,Human_Splice_Rec_1183910,Human_Splice_Rec_1183911,Human_Splice_Rec_1183942,Human_Splice_Rec_1183943,Human_Splice_Rec_1183973 RMVar_hsa_circ_146860,RMVar_hsa_circ_124449 68145 RMVar_ID_68145 Human_SNP_ID_449743607 m1A Human chr10 + 122211270 122211270 122211270 GGACAAGAGTAGTTGGGACAACCAGCAGGAAAACCCCCCTCCTACCAAAAAGATAGGCAAAAAGC GGACAAGAGTAGTTGGGACAACCAGCAGGAAACCCCCCCTCCTACCAAAAAGATAGGCAAAAAGC A C TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:122211225..122211461 26863196 MeRIP-seq:(Medium) rs1487895676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520361,Human_RBP_ID_9360917 RMVar_hsa_circ_68929,RMVar_hsa_circ_75124,RMVar_hsa_circ_24447,RMVar_hsa_circ_52822 68146 RMVar_ID_68146 Human_SNP_ID_449743654 m1A Human chr10 + 122211401 122211401 122211401 CTGCCTCACCTCCCAGATCCCCTGCTGAACCCAATGACATCCCCATTGCTAAAGGTACTTACACC CTGCCTCACCTCCCAGATCCCCTGCTGAACCCGATGACATCCCCATTGCTAAAGGTACTTACACC A G TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:122211351..122211425 26863196 MeRIP-seq:(Medium) rs1360376530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9360919,Human_RBP_ID_18931954,Human_RBP_ID_27404431 Human_Splice_Rec_1184007 RMVar_hsa_circ_68929,RMVar_hsa_circ_75124,RMVar_hsa_circ_24447,RMVar_hsa_circ_52822 68147 RMVar_ID_68147 Human_SNP_ID_449750396 m1A Human chr10 + 122238027 122238027 122238027 AAGATAAATATGAAGAAAGCAGGCGGGAAGTGATGGAAATGAGGTCAGTTGGGGAGCTGGGCCTT AAGATAAATATGAAGAAAGCAGGCGGGAAGTGTTGGAAATGAGGTCAGTTGGGGAGCTGGGCCTT A T TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122237976..122238050 26863196 MeRIP-seq:(Medium) rs978317426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862948,Human_RBP_ID_5341010,Human_RBP_ID_19045940 Human_Splice_Rec_1183518,Human_Splice_Rec_1183519,Human_Splice_Rec_1183560,Human_Splice_Rec_1183561,Human_Splice_Rec_1183598,Human_Splice_Rec_1183599,Human_Splice_Rec_1183636,Human_Splice_Rec_1183637,Human_Splice_Rec_1183688,Human_Splice_Rec_1183689,Human_Splice_Rec_1183724,Human_Splice_Rec_1183725,Human_Splice_Rec_1183760,Human_Splice_Rec_1183761,Human_Splice_Rec_1183802,Human_Splice_Rec_1183803,Human_Splice_Rec_1183834,Human_Splice_Rec_1183835,Human_Splice_Rec_1183864,Human_Splice_Rec_1183865,Human_Splice_Rec_1183898,Human_Splice_Rec_1183899,Human_Splice_Rec_1183930,Human_Splice_Rec_1183931,Human_Splice_Rec_1183962,Human_Splice_Rec_1183963,Human_Splice_Rec_1183996,Human_Splice_Rec_1183997,Human_Splice_Rec_1184043,Human_Splice_Rec_1184051 RMVar_hsa_circ_146862,RMVar_hsa_circ_42407,RMVar_hsa_circ_348630 68148 RMVar_ID_68148 Human_SNP_ID_449752989 m1A Human chr10 + 122248801 122248801 122248801 AGAAGATGAAGGAGGTCCTAGAAGGCTTCCGCAAGGTAGGGCTGAGTTTGGGGGCCACGGAGGAG AGAAGATGAAGGAGGTCCTAGAAGGCTTCCGCCAGGTAGGGCTGAGTTTGGGGGCCACGGAGGAG A C TACC2 Ensembl:ENSG00000138162 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122248751..122248825 26863196 MeRIP-seq:(Medium) rs755599004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18971378 Human_Splice_Rec_1183523,Human_Splice_Rec_1183565,Human_Splice_Rec_1183603,Human_Splice_Rec_1183641,Human_Splice_Rec_1183693,Human_Splice_Rec_1183729,Human_Splice_Rec_1183765,Human_Splice_Rec_1183807,Human_Splice_Rec_1183839,Human_Splice_Rec_1183869,Human_Splice_Rec_1183903,Human_Splice_Rec_1183935,Human_Splice_Rec_1183967,Human_Splice_Rec_1184001,Human_Splice_Rec_1184047,Human_Splice_Rec_1184057,Human_Splice_Rec_1184065,Human_Splice_Rec_1184067 RMVar_hsa_circ_146862,RMVar_hsa_circ_42407,RMVar_hsa_circ_146863 68149 RMVar_ID_68149 Human_SNP_ID_449753217 m1A Human chr10 + 122249511 122249510 122249512 GGAAGCAGGAGGTGTCTCTAGTGATCCACAAAAGAGTGATAATTCTGAGCTCCCTGTCTCCGCAG GGAAGCAGGAGGTGTCTCTAGTGATCCACAAA__AGTGATAATTCTGAGCTCCCTGTCTCCGCAG AAG A TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122249509..122249675 26863196 MeRIP-seq:(Medium) rs1242248056 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_146862 68150 RMVar_ID_68150 Human_SNP_ID_449753218 m1A Human chr10 + 122249511 122249511 122249511 GGAAGCAGGAGGTGTCTCTAGTGATCCACAAAAGAGTGATAATTCTGAGCTCCCTGTCTCCGCAG GGAAGCAGGAGGTGTCTCTAGTGATCCACAAAGGAGTGATAATTCTGAGCTCCCTGTCTCCGCAG A G TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122249509..122249675 26863196 MeRIP-seq:(Medium) rs1293504276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146862 68151 RMVar_ID_68151 Human_SNP_ID_449754368 m1A Human chr10 - 122253930 122253930 122253930 TGATGTTTGAAATCTGGCCAGTCAGAATGCTCATGGGGCTTTTTGGGGAGATGGGGGACCACCAG TGATGTTTGAAATCTGGCCAGTCAGAATGCTCGTGGGGCTTTTTGGGGAGATGGGGGACCACCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:122253928..122254011 26863196 MeRIP-seq:(Medium) rs527511669 Functional Loss SNV dbSNP153 33..33 33 - - - 68152 RMVar_ID_68152 Human_SNP_ID_449783532 m1A Human chr10 + 122374764 122374764 122374764 GACGCCGCTCCGGGCAGCCGAGCCTCTGTGGGAGCCGGGGCCGCGGCGGCGCGGGTGCTCCGGGC GACGCCGCTCCGGGCAGCCGAGCCTCTGTGGGGGCCGGGGCCGCGGCGGCGCGGGTGCTCCGGGC A G PLEKHA1 Ensembl:ENSG00000107679 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:122374723..122374970 26863196 MeRIP-seq:(Medium) rs988768997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225713,Human_RBP_ID_3364191,Human_RBP_ID_4136075,Human_RBP_ID_5163601,Human_RBP_ID_9413209,Human_RBP_ID_18416195 Human_Splice_Rec_1184131,Human_Splice_Rec_1184139,Human_Splice_Rec_1184161 68153 RMVar_ID_68153 Human_SNP_ID_449804643 m1A Human chr10 - 122461618 122461618 122461618 CGACTCTGGCGGCGGCGGCGGTGGCGGCGGACAGGGCGAGGGCCGGAGAGCGGCGCCGGGGAGAG CGACTCTGGCGGCGGCGGCGGTGGCGGCGGACGGGGCGAGGGCCGGAGAGCGGCGCCGGGGAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr10:122461515..122462082;chr10:122461576..122462000;chr10:122461513..122462057 26863196 MeRIP-seq:(Medium) rs1459876637 Functional Loss SNV dbSNP153 33..33 33 - - - 68154 RMVar_ID_68154 Human_SNP_ID_449804666 m1A Human chr10 + 122461646 122461646 122461646 GCCCTGTCCGCCGCCACCGCCGCCGCCGCCAGAGTCGCCATGCAGATCCCGCGCGCCGCTCTTCT GCCCTGTCCGCCGCCACCGCCGCCGCCGCCAGGGTCGCCATGCAGATCCCGCGCGCCGCTCTTCT A G HTRA1 Ensembl:ENSG00000166033 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr10:122461576..122461725;chr10:122461476..122461680 26863196,26863410 MeRIP-seq:(Medium) rs1429059351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2250107,Human_miRNA_ID_2784051 RMVar_hsa_circ_93885,RMVar_hsa_circ_146879 68155 RMVar_ID_68155 Human_SNP_ID_449804863 m1A Human chr10 - 122461978 122461976 122461978 CGCACACCGGCTCGCTGCTGGCGCACACACAGAGGCCGGCCTGCGCGCGCCGCCGCACCGTGGCC CGCACACCGGCTCGCTGCTGGCGCACACACAG__GCCGGCCTGCGCGCGCCGCCGCACCGTGGCC CCT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:122461843..122462050 26863196 MeRIP-seq:(Medium) rs1268315449 Functional Loss DEL dbSNP153 33..34 33 - - - 68156 RMVar_ID_68156 Human_SNP_ID_449815791 m1A Human chr10 + 122506793 122506793 122506793 GAAGCCCGTTTTCCCTTCAAAACACAGTCACCACCGGGATCGTGAGCACCACCCAGCGAGGCGGC GAAGCCCGTTTTCCCTTCAAAACACAGTCACCGCCGGGATCGTGAGCACCACCCAGCGAGGCGGC A G HTRA1 Ensembl:ENSG00000166033 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:122506744..122506864;chr10:122506744..122506831 26863196 MeRIP-seq:(Medium) rs1378497929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1184283,Human_Splice_Rec_1184299,Human_Splice_Rec_1184309 RMVar_hsa_circ_45359,RMVar_hsa_circ_93885,RMVar_hsa_circ_114105,RMVar_hsa_circ_146879,RMVar_hsa_circ_146880,RMVar_hsa_circ_146881,RMVar_hsa_circ_97369,RMVar_hsa_circ_82109,RMVar_hsa_circ_146882,RMVar_hsa_circ_146883 68157 RMVar_ID_68157 Human_SNP_ID_449901326 m1A Human chr10 + 122853340 122853340 122853340 ACCCTGGGCCCTTCGCATGTGTTATCCAGCCCATATCTCAACATAACATCTTTCCAGCCTCATCT ACCCTGGGCCCTTCGCATGTGTTATCCAGCCCGTATCTCAACATAACATCTTTCCAGCCTCATCT A G lnc-FAM24A-1 RNACentral:URS00009BB96E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:122853291..122853517;chr10:122853292..122853513 26863196 MeRIP-seq:(Medium) rs1235755169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101810,RMVar_hsa_circ_146901 68158 RMVar_ID_68158 Human_SNP_ID_449907190 m1A Human chr10 - 122879523 122879523 122879523 TTCGACGCTGGCGGTGGACGCAGGCAGCATGGACCACGGTTGCTGGGCGGATGGGGAGCGTCTAT TTCGACGCTGGCGGTGGACGCAGGCAGCATGGGCCACGGTTGCTGGGCGGATGGGGAGCGTCTAT T C AC073585.1,FAM24B Ensembl:ENSG00000286088,Ensembl:ENSG00000213185 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:122855697..122879560 26863196 MeRIP-seq:(Medium) rs760846203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22029592 Human_Splice_Rec_1185789,Human_Splice_Rec_1185809,Human_Splice_Rec_1185815,Human_Splice_Rec_1185819,Human_Splice_Rec_1185825 RMVar_hsa_circ_113382,RMVar_hsa_circ_146900 68159 RMVar_ID_68159 Human_SNP_ID_449907191 m1A Human chr10 - 122879527 122879527 122879527 GTTTTTCGACGCTGGCGGTGGACGCAGGCAGCATGGACCACGGTTGCTGGGCGGATGGGGAGCGT GTTTTTCGACGCTGGCGGTGGACGCAGGCAGCGTGGACCACGGTTGCTGGGCGGATGGGGAGCGT T C AC073585.1,FAM24B Ensembl:ENSG00000286088,Ensembl:ENSG00000213185 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122879437..122879547 26863196 MeRIP-seq:(Medium) rs1047410967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4110861,Human_RBP_ID_22029592 Human_Splice_Rec_1185789,Human_Splice_Rec_1185809,Human_Splice_Rec_1185815,Human_Splice_Rec_1185819,Human_Splice_Rec_1185825 RMVar_hsa_circ_113382,RMVar_hsa_circ_146900 68160 RMVar_ID_68160 Human_SNP_ID_449907192 m1A Human chr10 - 122879527 122879527 122879527 GTTTTTCGACGCTGGCGGTGGACGCAGGCAGCATGGACCACGGTTGCTGGGCGGATGGGGAGCGT GTTTTTCGACGCTGGCGGTGGACGCAGGCAGCCTGGACCACGGTTGCTGGGCGGATGGGGAGCGT T G AC073585.1,FAM24B Ensembl:ENSG00000286088,Ensembl:ENSG00000213185 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:122879437..122879547 26863196 MeRIP-seq:(Medium) rs1047410967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4110861,Human_RBP_ID_22029592 Human_Splice_Rec_1185789,Human_Splice_Rec_1185809,Human_Splice_Rec_1185815,Human_Splice_Rec_1185819,Human_Splice_Rec_1185825 RMVar_hsa_circ_113382,RMVar_hsa_circ_146900 68161 RMVar_ID_68161 Human_SNP_ID_449907296 m1A Human chr10 - 122879798 122879798 122879798 CTCTCTTCCAGTGCTTAAGTGTCGGCCAGTGCAGCGCAGAAACGGGCAGGCAGAGCGACTCCCGG CTCTCTTCCAGTGCTTAAGTGTCGGCCAGTGCGGCGCAGAAACGGGCAGGCAGAGCGACTCCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:122879757..122879998;chr10:122879751..122880287 26863196 MeRIP-seq:(Medium) rs1389050908 Functional Loss SNV dbSNP153 33..33 33 - - - 68162 RMVar_ID_68162 Human_SNP_ID_449924708 m1A Human chr10 - 122954159 122954159 122954159 TGAAGGCGGCGGAATGGAGACGCGGACCGAGGACGGGGGCCTCACCCGCCGCCCCACGCTGGCCT TGAAGGCGGCGGAATGGAGACGCGGACCGAGGGCGGGGGCCTCACCCGCCGCCCCACGCTGGCCT T C C10orf88 Ensembl:ENSG00000119965 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:122953880..122954163 26863196 MeRIP-seq:(Medium) rs1226435862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4110939,Human_RBP_ID_9361737 68163 RMVar_ID_68163 Human_SNP_ID_449924715 m1A Human chr10 - 122954166 122954166 122954166 GCCTGACTGAAGGCGGCGGAATGGAGACGCGGACCGAGGACGGGGGCCTCACCCGCCGCCCCACG GCCTGACTGAAGGCGGCGGAATGGAGACGCGGGCCGAGGACGGGGGCCTCACCCGCCGCCCCACG T C C10orf88 Ensembl:ENSG00000119965 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:122953023..122954205;chr10:122954094..122954198 26863196 MeRIP-seq:(Medium) rs769874307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9361737 68164 RMVar_ID_68164 Human_SNP_ID_449937341 m1A Human chr10 + 123008673 123008650 123008674 TCCGCCCTGTCCTGCCGCGTCGCCGCCGTCCGAGCCGGCAGCCTGCTACTTACCTCCTGACAACT TCCGCCCTGT________________________CCGGCAGCCTGCTACTTACCTCCTGACAACT TCCTGCCGCGTCGCCGCCGTCCGAG T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:123008665..123008753 26863410 MeRIP-seq:(Medium) rs773839189 Functional Loss DEL dbSNP153 11..34 33 - - - 68165 RMVar_ID_68165 Human_SNP_ID_449937364 m1A Human chr10 - 123008731 123008731 123008731 GACGAAGACGGCGGCGGCGGCGACGGCATTTAACAAGGCGGTGTGGTTTACTCCATGCAGTTGTC GACGAAGACGGCGGCGGCGGCGACGGCATTTACCAAGGCGGTGTGGTTTACTCCATGCAGTTGTC T G IKZF5 Ensembl:ENSG00000095574 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:123007163..123008817 26863196 MeRIP-seq:(Medium) rs1302750738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4111002,Human_RBP_ID_9360929,Human_RBP_ID_26316794 Human_Splice_Rec_1185955,Human_Splice_Rec_1185971,Human_Splice_Rec_1185977,Human_Splice_Rec_1185981 68166 RMVar_ID_68166 Human_SNP_ID_449937383 m1A Human chr10 + 123008770 123008770 123008770 CCGTCGCCGCCGCCGCCGTCTTCGTCACCGTCACAGTCGCCGCCGCCATCTTTGTTGTGTCTCCG CCGTCGCCGCCGCCGCCGTCTTCGTCACCGTCCCAGTCGCCGCCGCCATCTTTGTTGTGTCTCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:123008537..123008840 26863196 MeRIP-seq:(Medium) rs1479005086 Functional Loss SNV dbSNP153 33..33 33 - - - 68167 RMVar_ID_68167 Human_SNP_ID_449937384 m1A Human chr10 + 123008770 123008770 123008770 CCGTCGCCGCCGCCGCCGTCTTCGTCACCGTCACAGTCGCCGCCGCCATCTTTGTTGTGTCTCCG CCGTCGCCGCCGCCGCCGTCTTCGTCACCGTCTCAGTCGCCGCCGCCATCTTTGTTGTGTCTCCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:123008537..123008840 26863196 MeRIP-seq:(Medium) rs1479005086 Functional Loss SNV dbSNP153 33..33 33 - - - 68168 RMVar_ID_68168 Human_SNP_ID_449969025 m1A Human chr10 - 123136364 123136364 123136364 AGGCTGGGGAGCGCTCCAGGTAGTGCGCGGGCAGGGCAAACCTCTGCGCCGGGATCTCAAAGCGA AGGCTGGGGAGCGCTCCAGGTAGTGCGCGGGCGGGGCAAACCTCTGCGCCGGGATCTCAAAGCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:123135936..123136391;chr10:123136219..123136382 26863196 MeRIP-seq:(Medium) rs1489314594 Functional Loss SNV dbSNP153 33..33 33 - - - 68169 RMVar_ID_68169 Human_SNP_ID_449974562 m1A Human chr10 + 123154886 123154871 123154886 CAGGCTGTCAGTGCGCAGCCCCAGCCCGCGGGACCCCTGGGGACTCTGGGCGCCTGTTCTGCAGA CAGGCTGTCAGTGCGCAG_______________CCCCTGGGGACTCTGGGCGCCTGTTCTGCAGA GCCCCAGCCCGCGGGA G BUB3 Ensembl:ENSG00000154473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:123154878..123155052 26863196 MeRIP-seq:(Medium) rs778591386 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_22029601 RMVar_hsa_circ_120385,RMVar_hsa_circ_146914,RMVar_hsa_circ_91366,RMVar_hsa_circ_146913 68170 RMVar_ID_68170 Human_SNP_ID_449974630 m1A Human chr10 + 123155026 123155026 123155026 CCTCCCAGTTCCTGCTTGTCTCCTCCTGGGACACGTCCGTGCGTCTCTACGATGTGCCGGCCAAC CCTCCCAGTTCCTGCTTGTCTCCTCCTGGGACGCGTCCGTGCGTCTCTACGATGTGCCGGCCAAC A G BUB3 Ensembl:ENSG00000154473 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:123154426..123157746 32194978 MeRIP-seq:(Medium) rs761397969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4111075,Human_RBP_ID_8328157,Human_RBP_ID_18588842,Human_RBP_ID_22431614,Human_RBP_ID_22787763 Human_Splice_Rec_1186035,Human_Splice_Rec_1186043,Human_Splice_Rec_1186057,Human_Splice_Rec_1186069 RMVar_hsa_circ_351,RMVar_hsa_circ_88516,RMVar_hsa_circ_120385,RMVar_hsa_circ_146914,RMVar_hsa_circ_91366,RMVar_hsa_circ_146913,RMVar_hsa_circ_7997,RMVar_hsa_circ_146915 68171 RMVar_ID_68171 Human_SNP_ID_449975932 m1A Human chr10 - 123160567 123160567 123160567 AATTCCAGAAAGAAGAGGAGGTATAGTTCAATACCTGCTTGTTTGGAAACGCTCGTATGCAGCGA AATTCCAGAAAGAAGAGGAGGTATAGTTCAATGCCTGCTTGTTTGGAAACGCTCGTATGCAGCGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:123160521..123162292 32194978 MeRIP-seq:(Medium) rs1420853075 Functional Loss SNV dbSNP153 33..33 33 - - - 68172 RMVar_ID_68172 Human_SNP_ID_450203295 m1A Human chr10 + 124092239 124092239 124092239 ACCCAACAGACTCGCATTACATCTCCACCGCCAGCGTCGCCTCCGCGCCCCGGCCGCTGCCATCC ACCCAACAGACTCGCATTACATCTCCACCGCCGGCGTCGCCTCCGCGCCCCGGCCGCTGCCATCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:124092142..124092278 26863196 MeRIP-seq:(Medium) rs888875405 Functional Loss SNV dbSNP153 33..33 33 - - - 68173 RMVar_ID_68173 Human_SNP_ID_450203565 m1A Human chr10 - 124093160 124093160 124093160 CGGGCTCCTTGGCCCGGCCTCCCCGAGGCTTCAGCGATCCCCAGCGGGAGGAGTCCCTTCGCCAT CGGGCTCCTTGGCCCGGCCTCCCCGAGGCTTCGGCGATCCCCAGCGGGAGGAGTCCCTTCGCCAT T C CHST15 Ensembl:ENSG00000182022 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:124093134..124093385 26863196 MeRIP-seq:(Medium) rs1374105553 Functional Loss SNV dbSNP153 33..33 33 - - - 68174 RMVar_ID_68174 Human_SNP_ID_450203612 m1A Human chr10 + 124093283 124093283 124093283 GCCGCCACCGCCACCGCCACCACCGCGCCGGGAGCGCCGCGGGGAGTGAGGCTGCGCGCCGCCTC GCCGCCACCGCCACCGCCACCACCGCGCCGGGGGCGCCGCGGGGAGTGAGGCTGCGCGCCGCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:124093157..124093316 26863196 MeRIP-seq:(Medium) rs1281916024 Functional Loss SNV dbSNP153 33..33 33 - - - 68175 RMVar_ID_68175 Human_SNP_ID_450203685 m1A Human chr10 - 124093540 124093540 124093540 GTCAGGTTGACGCGCCCTGGATGCGGGGCTAGAGGCTCGGGGCTGGGCGCGCTCCCGCGGAGCCG GTCAGGTTGACGCGCCCTGGATGCGGGGCTAGCGGCTCGGGGCTGGGCGCGCTCCCGCGGAGCCG T G CHST15 Ensembl:ENSG00000182022 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124093419..124093585 26863196 MeRIP-seq:(Medium) rs1463077275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364954,Human_RBP_ID_4111235,Human_RBP_ID_18416401,Human_RBP_ID_18456206,Human_RBP_ID_22431892,Human_RBP_ID_22537129,Human_RBP_ID_23441543 Human_Splice_Rec_1186281,Human_Splice_Rec_1186307 68176 RMVar_ID_68176 Human_SNP_ID_450278284 m1A Human chr10 + 124398100 124398100 124398100 TCGAAGTCGTAGACACACCTTCCAAGCATCCCAATCTAAAGAAAAATAGTAAAACGTACATGCTC TCGAAGTCGTAGACACACCTTCCAAGCATCCCCATCTAAAGAAAAATAGTAAAACGTACATGCTC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:124397850..124398100 32194978 MeRIP-seq:(Medium) rs1029733427 Functional Loss SNV dbSNP153 33..33 33 - - - 68177 RMVar_ID_68177 Human_SNP_ID_450283881 m1A Human chr10 + 124418782 124418759 124418783 CAGCCAGCATCCCCCGAACCCGGGCCGCGGCCACCCCGCGCCCGCCCGCCTCCCCCGCCGCTGTC CAGCCAGCAT________________________CCCGCGCCCGCCCGCCTCCCCCGCCGCTGTC TCCCCCGAACCCGGGCCGCGGCCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124418769..124418877 26863196 MeRIP-seq:(Medium) rs1288540281 Functional Loss DEL dbSNP153 11..34 33 - - - 68178 RMVar_ID_68178 Human_SNP_ID_450283883 m1A Human chr10 + 124418767 124418767 124418767 CCCAGCGCGCCCCCTCAGCCAGCATCCCCCGAACCCGGGCCGCGGCCACCCCGCGCCCGCCCGCC CCCAGCGCGCCCCCTCAGCCAGCATCCCCCGACCCCGGGCCGCGGCCACCCCGCGCCCGCCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:124418762..124418861 26863196 MeRIP-seq:(Medium) rs1435890739 Functional Loss SNV dbSNP153 33..33 33 - - - 68179 RMVar_ID_68179 Human_SNP_ID_450297246 m1A Human chr10 - 124467167 124467167 124467167 TACTGCCAGCCTGTTCTCCACACTGCAGCCAGAGAGATCTCCTTGAAATATTTTATTTAAAAAAC TACTGCCAGCCTGTTCTCCACACTGCAGCCAGCGAGATCTCCTTGAAATATTTTATTTAAAAAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:124467165..124467323 26863196 MeRIP-seq:(Medium) rs932030702 Functional Loss SNV dbSNP153 33..33 33 - - - 68180 RMVar_ID_68180 Human_SNP_ID_450306372 m1A Human chr10 - 124498061 124498061 124498061 ACTTGAAAAACTCAGGAGAAGGCTTCCCCACCACCTCGGCTTTGATGCCACAGGCATACTGGGAA ACTTGAAAAACTCAGGAGAAGGCTTCCCCACCTCCTCGGCTTTGATGCCACAGGCATACTGGGAA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:124497000..124498111 32194978 MeRIP-seq:(Medium) rs1309201353 Functional Loss SNV dbSNP153 33..33 33 - - - 68181 RMVar_ID_68181 Human_SNP_ID_450306373 m1A Human chr10 - 124498061 124498061 124498061 ACTTGAAAAACTCAGGAGAAGGCTTCCCCACCACCTCGGCTTTGATGCCACAGGCATACTGGGAA ACTTGAAAAACTCAGGAGAAGGCTTCCCCACCGCCTCGGCTTTGATGCCACAGGCATACTGGGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:124497000..124498111 32194978 MeRIP-seq:(Medium) rs1309201353 Functional Loss SNV dbSNP153 33..33 33 - - - 68182 RMVar_ID_68182 Human_SNP_ID_450306421 m1A Human chr10 + 124498165 124498165 124498165 GTTGGCGCCTTGTGAAGTGGGTCAGGGGAGGCAGCCCCGTCAGGGAGGCCCTGGAGCTTGGAATG GTTGGCGCCTTGTGAAGTGGGTCAGGGGAGGCCGCCCCGTCAGGGAGGCCCTGGAGCTTGGAATG A C LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124498161..124498237 26863196 MeRIP-seq:(Medium) rs3832703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5234651 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68183 RMVar_ID_68183 Human_SNP_ID_450309055 m1A Human chr10 + 124506987 124506938 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA _________________________________GGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA GGGGGGGTAGGGAGGATTTCAGGTGGGCGGGTAGACAGGATTTCAGGTGA G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1216149629 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68184 RMVar_ID_68184 Human_SNP_ID_450309085 m1A Human chr10 + 124506987 124506962 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTG_________________________GGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA GGGCGGGTAGACAGGATTTCAGGTGA G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1390218854 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68185 RMVar_ID_68185 Human_SNP_ID_450309113 m1A Human chr10 + 124506987 124506985 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTGGGCGGGTAGACAGGATTTCAGGT__GGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TGA T LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs201373067 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68186 RMVar_ID_68186 Human_SNP_ID_450309117 m1A Human chr10 + 124506987 124506986 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTGGGCGGGTAGACAGGATTTCAGGTG_GGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA GA G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1387807450 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68187 RMVar_ID_68187 Human_SNP_ID_450309121 m1A Human chr10 + 124506987 124506987 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGCGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA A C LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1330746030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68188 RMVar_ID_68188 Human_SNP_ID_450309122 m1A Human chr10 + 124506987 124506987 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGGGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1330746030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68189 RMVar_ID_68189 Human_SNP_ID_450309123 m1A Human chr10 + 124506987 124506987 124506987 TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGAGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA TTCAGGTGGGCGGGTAGACAGGATTTCAGGTGTGGGGGGTAGGGAGGATTTCAGGTCGGGGGGTA A T LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:124506943..124507143 26863196 MeRIP-seq:(Medium) rs1330746030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5163294 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 68190 RMVar_ID_68190 Human_SNP_ID_450336847 m1A Human chr10 - 124610354 124610342 124610354 CCCTCACCCGCTCCACCAGCACCCTCACCCGCACCCTCACCCGCTCCATCAGCACCCTCACCCGC CCCTCACCCGCTCCACCAGCACCCTCACCCGC____________TCCATCAGCACCCTCACCCGC AGCGGGTGAGGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124610350..124610420 26863196 MeRIP-seq:(Medium) rs1339298459 Functional Loss DEL dbSNP153 33..44 33 - - - 68191 RMVar_ID_68191 Human_SNP_ID_450336857 m1A Human chr10 - 124610354 124610354 124610354 CCCTCACCCGCTCCACCAGCACCCTCACCCGCACCCTCACCCGCTCCATCAGCACCCTCACCCGC CCCTCACCCGCTCCACCAGCACCCTCACCCGCTCCCTCACCCGCTCCATCAGCACCCTCACCCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124610350..124610420 26863196 MeRIP-seq:(Medium) rs201250786 Functional Loss SNV dbSNP153 33..33 33 - - - 68192 RMVar_ID_68192 Human_SNP_ID_450338072 m1A Human chr10 + 124613656 124613655 124613656 CAGCTCCCTGTAGTGAAGTCCAGGAGGGTGGGACAGGCCTGTCAGGCCTCTGGGAATCTCCCAAA CAGCTCCCTGTAGTGAAGTCCAGGAGGGTGGG_CAGGCCTGTCAGGCCTCTGGGAATCTCCCAAA GA G LHPP Ensembl:ENSG00000107902 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:124612948..124613708 32194978 MeRIP-seq:(Medium) rs1405741377 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26398768 RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_86169,RMVar_hsa_circ_113672,RMVar_hsa_circ_146946,RMVar_hsa_circ_112196,RMVar_hsa_circ_91725,RMVar_hsa_circ_146947,RMVar_hsa_circ_146948,RMVar_hsa_circ_146949 68193 RMVar_ID_68193 Human_SNP_ID_450356196 m1A Human chr10 - 124681774 124681774 124681774 TTTCCTTTGTGGAATACTGTCCTCCCTCAGCCAACAGCACACCTGCCTCAACACCAGAGCTGGCG TTTCCTTTGTGGAATACTGTCCTCCCTCAGCCGACAGCACACCTGCCTCAACACCAGAGCTGGCG T C AC068896.3,FAM53B Ensembl:ENSG00000258539,Ensembl:ENSG00000189319 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:124681726..124681926 32194978 MeRIP-seq:(Medium) rs771601140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22027362,Human_RBP_ID_22151334,Human_RBP_ID_27404568 RMVar_hsa_circ_91458,RMVar_hsa_circ_90401,RMVar_hsa_circ_146950,RMVar_hsa_circ_146957,RMVar_hsa_circ_102054,RMVar_hsa_circ_146951,RMVar_hsa_circ_83315,RMVar_hsa_circ_146952,RMVar_hsa_circ_276282,RMVar_hsa_circ_146955,RMVar_hsa_circ_100027,RMVar_hsa_circ_146956,RMVar_hsa_circ_295446,RMVar_hsa_circ_333711,RMVar_hsa_circ_146959,RMVar_hsa_circ_275512,RMVar_hsa_circ_146958 68194 RMVar_ID_68194 Human_SNP_ID_450369231 m1A Human chr10 - 124733929 124733929 124733929 TGTCCCCAGTCACAGCACCATGGGACTGTGTCAGGGAATCTGGGAGACCTGGAGCCTGAGTGAGA TGTCCCCAGTCACAGCACCATGGGACTGTGTCGGGGAATCTGGGAGACCTGGAGCCTGAGTGAGA T C AC068896.3,FAM53B Ensembl:ENSG00000258539,Ensembl:ENSG00000189319 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124733924..124734015 26863196 MeRIP-seq:(Medium) rs1223943205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83315,RMVar_hsa_circ_146952,RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_146962,RMVar_hsa_circ_111316,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_104027,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146965 68195 RMVar_ID_68195 Human_SNP_ID_450371894 m1A Human chr10 - 124744117 124744117 124744117 GGAGTCGCTCGTACAAAGCGCTCGGCGCCGGCAGGCGAGCGTGCGCGCGGCGGACGCGCGGCGGG GGAGTCGCTCGTACAAAGCGCTCGGCGCCGGCCGGCGAGCGTGCGCGCGGCGGACGCGCGGCGGG T G AC068896.3,FAM53B Ensembl:ENSG00000258539,Ensembl:ENSG00000189319 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:124744066..124744292 26863196 MeRIP-seq:(Medium) rs1258763934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4111456 RMVar_hsa_circ_83315,RMVar_hsa_circ_146952,RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_146962,RMVar_hsa_circ_111316,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_104027,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146965 68196 RMVar_ID_68196 Human_SNP_ID_450375639 m1A Human chr10 + 124760462 124760462 124760462 TGCTGCTACACTGTTTCCAGATCTGCCTCCAAAGCTGAACTTGGGTGTTGGTAGCTCTTCGAGAA TGCTGCTACACTGTTTCCAGATCTGCCTCCAACGCTGAACTTGGGTGTTGGTAGCTCTTCGAGAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:124760417..124765455 32194978 MeRIP-seq:(Medium) rs988330083 Functional Loss SNV dbSNP153 33..33 33 - - - 68197 RMVar_ID_68197 Human_SNP_ID_450375640 m1A Human chr10 + 124760462 124760462 124760462 TGCTGCTACACTGTTTCCAGATCTGCCTCCAAAGCTGAACTTGGGTGTTGGTAGCTCTTCGAGAA TGCTGCTACACTGTTTCCAGATCTGCCTCCAAGGCTGAACTTGGGTGTTGGTAGCTCTTCGAGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:124760417..124765455 32194978 MeRIP-seq:(Medium) rs988330083 Functional Loss SNV dbSNP153 33..33 33 - - - 68198 RMVar_ID_68198 Human_SNP_ID_450383951 m1A Human chr10 - 124790333 124790333 124790333 TTGCTTTGCATTTCATTGTTTACATAGTTGGGATGCTGTCTATGAGAGAGAACTGCAAACTTTCC TTGCTTTGCATTTCATTGTTTACATAGTTGGGTTGCTGTCTATGAGAGAGAACTGCAAACTTTCC T A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124790276..124790389 26863196 MeRIP-seq:(Medium) rs1028912072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136556,Human_RBP_ID_5339768,Human_RBP_ID_5943911,Human_RBP_ID_8328795,Human_RBP_ID_11300319,Human_RBP_ID_22639723,Human_RBP_ID_23442008 Human_Splice_Rec_1186440,Human_Splice_Rec_1186441,Human_Splice_Rec_1186492,Human_Splice_Rec_1186493,Human_Splice_Rec_1186502,Human_Splice_Rec_1186503,Human_Splice_Rec_1186514,Human_Splice_Rec_1186515,Human_Splice_Rec_1186526,Human_Splice_Rec_1186527 RMVar_hsa_circ_4130,RMVar_hsa_circ_113129,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308,RMVar_hsa_circ_121172,RMVar_hsa_circ_9618,RMVar_hsa_circ_146974 68199 RMVar_ID_68199 Human_SNP_ID_450384323 m1A Human chr10 - 124791734 124791734 124791734 GGGAGGACGGTTTCGTCCCGTCGGCGCTGGGGACCCGCGAGCAGTGAGTGTGACGCTGGGCAGGG GGGAGGACGGTTTCGTCCCGTCGGCGCTGGGGCCCCGCGAGCAGTGAGTGTGACGCTGGGCAGGG T G EEF1AKMT2 Ensembl:ENSG00000203791 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:124790251..124791875 26863196 MeRIP-seq:(Medium) rs1238915830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373288,Human_RBP_ID_806254,Human_RBP_ID_861424,Human_RBP_ID_1351193,Human_RBP_ID_4136558,Human_RBP_ID_5943920,Human_RBP_ID_11300345,Human_RBP_ID_18416200,Human_RBP_ID_22886685 Human_Splice_Rec_1186439,Human_Splice_Rec_1186491,Human_Splice_Rec_1186501,Human_Splice_Rec_1186513,Human_Splice_Rec_1186525 RMVar_hsa_circ_121172,RMVar_hsa_circ_146974 68200 RMVar_ID_68200 Human_SNP_ID_450423291 m1A Human chr10 + 124942438 124942438 124942438 TTTGGAGGTGGAATGTAGTTATTTTAATAACCATGTCCTAATTATTTATAGCTTCCTGCCTGACA TTTGGAGGTGGAATGTAGTTATTTTAATAACCGTGTCCTAATTATTTATAGCTTCCTGCCTGACA A G ZRANB1,AL731577.2 Ensembl:ENSG00000019995,Ensembl:ENSG00000249456 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124942436..124942543 26863196 MeRIP-seq:(Medium) rs778024242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2196453,Human_RBP_ID_3342896,Human_RBP_ID_17595768 RMVar_hsa_circ_146983,RMVar_hsa_circ_89969,RMVar_hsa_circ_146982,RMVar_hsa_circ_146984,RMVar_hsa_circ_146985,RMVar_hsa_circ_378394 68201 RMVar_ID_68201 Human_SNP_ID_450450765 m1A Human chr10 - 125039061 125039061 125039061 TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCATAAAGAATGGCCCTTGTGGATAAGCACAAAGT TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCGTAAAGAATGGCCCTTGTGGATAAGCACAAAGT T C CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:125039011..125039200 26863196 MeRIP-seq:(Medium) rs76319950 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1443473,Human_RBP_ID_8328940,Human_RBP_ID_18589602 Human_Splice_Rec_1186602,Human_Splice_Rec_1186603,Human_Splice_Rec_1186638,Human_Splice_Rec_1186639,Human_Splice_Rec_1186658,Human_Splice_Rec_1186659,Human_Splice_Rec_1186678,Human_Splice_Rec_1186679,Human_Splice_Rec_1186708,Human_Splice_Rec_1186709,Human_Splice_Rec_1186716,Human_Splice_Rec_1186722 RMVar_hsa_circ_103784,RMVar_hsa_circ_110012,RMVar_hsa_circ_88110,RMVar_hsa_circ_147000,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002,RMVar_hsa_circ_110716,RMVar_hsa_circ_147003,RMVar_hsa_circ_47244,RMVar_hsa_circ_147004,RMVar_hsa_circ_125557,RMVar_hsa_circ_62045,RMVar_hsa_circ_80631,RMVar_hsa_circ_272393,RMVar_hsa_circ_286734,RMVar_hsa_circ_147005,RMVar_hsa_circ_280237,RMVar_hsa_circ_126097,RMVar_hsa_circ_147007,RMVar_hsa_circ_147009,RMVar_hsa_circ_147011,RMVar_hsa_circ_98565,RMVar_hsa_circ_147010,RMVar_hsa_circ_147008,RMVar_hsa_circ_147006 68202 RMVar_ID_68202 Human_SNP_ID_450450766 m1A Human chr10 - 125039061 125039061 125039061 TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCATAAAGAATGGCCCTTGTGGATAAGCACAAAGT TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCCTAAAGAATGGCCCTTGTGGATAAGCACAAAGT T G CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:125039011..125039200 26863196 MeRIP-seq:(Medium) rs76319950 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1443473,Human_RBP_ID_8328940,Human_RBP_ID_18589602 Human_Splice_Rec_1186602,Human_Splice_Rec_1186603,Human_Splice_Rec_1186638,Human_Splice_Rec_1186639,Human_Splice_Rec_1186658,Human_Splice_Rec_1186659,Human_Splice_Rec_1186678,Human_Splice_Rec_1186679,Human_Splice_Rec_1186708,Human_Splice_Rec_1186709,Human_Splice_Rec_1186716,Human_Splice_Rec_1186722 RMVar_hsa_circ_103784,RMVar_hsa_circ_110012,RMVar_hsa_circ_88110,RMVar_hsa_circ_147000,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002,RMVar_hsa_circ_110716,RMVar_hsa_circ_147003,RMVar_hsa_circ_47244,RMVar_hsa_circ_147004,RMVar_hsa_circ_125557,RMVar_hsa_circ_62045,RMVar_hsa_circ_80631,RMVar_hsa_circ_272393,RMVar_hsa_circ_286734,RMVar_hsa_circ_147005,RMVar_hsa_circ_280237,RMVar_hsa_circ_126097,RMVar_hsa_circ_147007,RMVar_hsa_circ_147009,RMVar_hsa_circ_147011,RMVar_hsa_circ_98565,RMVar_hsa_circ_147010,RMVar_hsa_circ_147008,RMVar_hsa_circ_147006 68203 RMVar_ID_68203 Human_SNP_ID_450463632 m1A Human chr10 + 125084720 125084720 125084720 CCCCTGGCAGAGGGTGGGTCTGGTATCTGTGTAGCAGGTCCTGACCCCACCCAAGCAGCAGCAGT CCCCTGGCAGAGGGTGGGTCTGGTATCTGTGTGGCAGGTCCTGACCCCACCCAAGCAGCAGCAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:125084718..125084819 26863196 MeRIP-seq:(Medium) rs559248803 Functional Loss SNV dbSNP153 33..33 33 - - - 68204 RMVar_ID_68204 Human_SNP_ID_450463648 m1A Human chr10 + 125084799 125084799 125084799 GCCTTCCTGACCCACCGGCACTCTTTCCCACCAAGACGCCTTGAGATCCCCAAAACACGTCTCCA GCCTTCCTGACCCACCGGCACTCTTTCCCACCGAGACGCCTTGAGATCCCCAAAACACGTCTCCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:125084792..125084921 26863196 MeRIP-seq:(Medium) rs3844601 Functional Loss SNV dbSNP153 33..33 33 - - - 68205 RMVar_ID_68205 Human_SNP_ID_450484097 m1A Human chr10 + 125159115 125159112 125159116 GCCCGGGGCGCTGGGGGCAGCGCGAGGGAGAGAAAGAAAGGCGCTTCCCCTCGGCCGCGCGGGGC GCCCGGGGCGCTGGGGGCAGCGCGAGGGAG____AGAAAGGCGCTTCCCCTCGGCCGCGCGGGGC GAGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:125159113..125159267 26863196 MeRIP-seq:(Medium) rs1394021750 Functional Loss DEL dbSNP153 31..34 33 - - - 68206 RMVar_ID_68206 Human_SNP_ID_450484532 m1A Human chr10 + 125160094 125160094 125160094 GCGGGCGCAATCGGTGGCGGGGGCGGGCGGGGACCCCCGAGCCAGCGTCCACCCCCGGGCGCCGA GCGGGCGCAATCGGTGGCGGGGGCGGGCGGGGCCCCCCGAGCCAGCGTCCACCCCCGGGCGCCGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:125160065..125160270 26863196 MeRIP-seq:(Medium) rs1009372442 Functional Loss SNV dbSNP153 33..33 33 - - - 68207 RMVar_ID_68207 Human_SNP_ID_450484664 m1A Human chr10 - 125160382 125160382 125160382 ACCGCCGCCGGGTGGGGTGGGAGGGGCGGGAGACGCCGCCGCCGCCGCCTCCAGGGTGGGCGCCT ACCGCCGCCGGGTGGGGTGGGAGGGGCGGGAGCCGCCGCCGCCGCCGCCTCCAGGGTGGGCGCCT T G CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:125160326..125160550 26863196 MeRIP-seq:(Medium) rs1201830329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373439,Human_RBP_ID_4139992,Human_RBP_ID_8059319,Human_RBP_ID_8172800,Human_RBP_ID_9320757,Human_RBP_ID_17345806,Human_RBP_ID_18476537,Human_RBP_ID_22708156 Human_Splice_Rec_1186599,Human_Splice_Rec_1186655,Human_Splice_Rec_1186715 RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 68208 RMVar_ID_68208 Human_SNP_ID_450484691 m1A Human chr10 - 125160420 125160420 125160420 CCGCGCTGAGGGGGGGCCGCACAGCCGCCGCCACCGCCACCGCCGCCGGGTGGGGTGGGAGGGGC CCGCGCTGAGGGGGGGCCGCACAGCCGCCGCCGCCGCCACCGCCGCCGGGTGGGGTGGGAGGGGC T C CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:125160300..125160577 26863410 MeRIP-seq:(Medium) rs192096344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18476538,Human_RBP_ID_22708156 RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 68209 RMVar_ID_68209 Human_SNP_ID_450484692 m1A Human chr10 - 125160420 125160420 125160420 CCGCGCTGAGGGGGGGCCGCACAGCCGCCGCCACCGCCACCGCCGCCGGGTGGGGTGGGAGGGGC CCGCGCTGAGGGGGGGCCGCACAGCCGCCGCCCCCGCCACCGCCGCCGGGTGGGGTGGGAGGGGC T G CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:125160300..125160577 26863410 MeRIP-seq:(Medium) rs192096344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18476538,Human_RBP_ID_22708156 RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 68210 RMVar_ID_68210 Human_SNP_ID_450484711 m1A Human chr10 + 125160454 125160454 125160454 GCGGCGGCTGTGCGGCCCCCCCTCAGCGCGGCATGGCTCCCGGTTCGGTCCCTCGCTCCTCGGGC GCGGCGGCTGTGCGGCCCCCCCTCAGCGCGGCGTGGCTCCCGGTTCGGTCCCTCGCTCCTCGGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:125160360..125160536 26863196 MeRIP-seq:(Medium) rs1269331948 Functional Loss SNV dbSNP153 33..33 33 - - - 68211 RMVar_ID_68211 Human_SNP_ID_450518807 m1A Human chr10 + 125300264 125300264 125300264 ATCCCAGCACTTTGGGCGGTCGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTG ATCCCAGCACTTTGGGCGGTCGAGGCGGGTGGGTCACCTGAGGTCAGGAGTTCGAGACCAGCCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:125300216..125300343 26863196 MeRIP-seq:(Medium) rs1014803110 Functional Loss SNV dbSNP153 33..33 33 - - - 68212 RMVar_ID_68212 Human_SNP_ID_450650434 m1A Human chr10 + 125823163 125823163 125823163 CAGGGGCGGAAGCCCCCTCCCCACGCAGCCCGAGGGGCCGCGGCGGCCACCCGCGCCGGGCCCCA CAGGGGCGGAAGCCCCCTCCCCACGCAGCCCGGGGGGCCGCGGCGGCCACCCGCGCCGGGCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:125823127..125823213 26863196 MeRIP-seq:(Medium) rs1161698054 Functional Loss SNV dbSNP153 33..33 33 - - - 68213 RMVar_ID_68213 Human_SNP_ID_450651413 m1A Human chr10 - 125826595 125826595 125826595 CTGATAGGGAATAAGCTTCAAATTCAATATTCACTTCCTGTAAATAACACACAAAATAGTTGTTA CTGATAGGGAATAAGCTTCAAATTCAATATTCGCTTCCTGTAAATAACACACAAAATAGTTGTTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:125826576..125826675 26863196 MeRIP-seq:(Medium) rs545503154 Functional Loss SNV dbSNP153 33..33 33 - - - 68214 RMVar_ID_68214 Human_SNP_ID_450926939 m1A Human chr10 + 126904237 126904237 126904237 AGCCCTGCTGTTCAGCACTGTCCCTACCTCACAGAGGTAGGGACCTCTTTTTCTTACCTTCTTCC AGCCCTGCTGTTCAGCACTGTCCCTACCTCACGGAGGTAGGGACCTCTTTTTCTTACCTTCTTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126904133..126904246 26863196 MeRIP-seq:(Medium) rs1231192641 Functional Loss SNV dbSNP153 33..33 33 - - - 68215 RMVar_ID_68215 Human_SNP_ID_450937794 m1A Human chr10 - 126945358 126945358 126945358 GTGACAAAACCAGCCCTACATGAGCTGCCCCTATGGAGAGGCCCACGTGGGAAGGAAATGCAAGT GTGACAAAACCAGCCCTACATGAGCTGCCCCTGTGGAGAGGCCCACGTGGGAAGGAAATGCAAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:126945347..126945543 26863196 MeRIP-seq:(Medium) rs1482386418 Functional Loss SNV dbSNP153 33..33 33 - - - 68216 RMVar_ID_68216 Human_SNP_ID_450937821 m1A Human chr10 + 126945460 126945455 126945461 GGGAGAGGGAAAGAGGGGAGAAGGGGAAAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC GGGAGAGGGAAAGAGGGGAGAAGGGGAA______AGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC AAGAGAG A DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126945457..126945549 26863196 MeRIP-seq:(Medium) rs1261260472 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_804874,Human_RBP_ID_5341029 68217 RMVar_ID_68217 Human_SNP_ID_450937822 m1A Human chr10 + 126945460 126945455 126945461 GGGAGAGGGAAAGAGGGGAGAAGGGGAAAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC GGGAGAGGGAAAGAGGGGAGAAGGGGAAAG____AGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC AAGAGAG AAG DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126945457..126945549 26863196 MeRIP-seq:(Medium) rs1261260472 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_804874,Human_RBP_ID_5341029 68218 RMVar_ID_68218 Human_SNP_ID_450937823 m1A Human chr10 + 126945460 126945455 126945461 GGGAGAGGGAAAGAGGGGAGAAGGGGAAAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC GGGAGAGGGAAAGAGGGGAGAAGGGGAAAGAG__AGAGAGAGAGGGAGAGAGAGAGAGAGAGTGC AAGAGAG AAGAG DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126945457..126945549 26863196 MeRIP-seq:(Medium) rs1261260472 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_804874,Human_RBP_ID_5341029 68219 RMVar_ID_68219 Human_SNP_ID_450940817 m1A Human chr10 + 126952847 126952844 126952847 TTGTTGGTGATGGTGGTGGTGGTAGTGTTGGTAGTATTGTTGGTGATGTGGTAGTATTGTTATTG TTGTTGGTGATGGTGGTGGTGGTAGTGTTG___GTATTGTTGGTGATGTGGTAGTATTGTTATTG GGTA G DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126952653..126952913 26863196 MeRIP-seq:(Medium) rs1164890744 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_804896,Human_RBP_ID_17107894 68220 RMVar_ID_68220 Human_SNP_ID_450940820 m1A Human chr10 + 126952847 126952847 126952847 TTGTTGGTGATGGTGGTGGTGGTAGTGTTGGTAGTATTGTTGGTGATGTGGTAGTATTGTTATTG TTGTTGGTGATGGTGGTGGTGGTAGTGTTGGTGGTATTGTTGGTGATGTGGTAGTATTGTTATTG A G DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:126952653..126952913 26863196 MeRIP-seq:(Medium) rs1418230932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804896,Human_RBP_ID_17107894 68221 RMVar_ID_68221 Human_SNP_ID_450940981 m1A Human chr10 + 126953309 126953309 126953309 TTGTGGTGTGGTGTGGTGGTAGTGGTGATGGCAGTGGAGGTGGTAGTGGTGGTAGTATTGTCAGT TTGTGGTGTGGTGTGGTGGTAGTGGTGATGGCTGTGGAGGTGGTAGTGGTGGTAGTATTGTCAGT A T DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:126953290..126953543 26863196 MeRIP-seq:(Medium) rs1212912634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804898,Human_RBP_ID_17107898 68222 RMVar_ID_68222 Human_SNP_ID_451036712 m1A Human chr10 + 127328592 127328591 127328592 ATGGCAGGGACGCCAGGGACAGCAAGGACGGCAGGGACGCCAGGGACGGCAGGGATGCGAGGGAC ATGGCAGGGACGCCAGGGACAGCAAGGACGGC_GGGACGCCAGGGACGGCAGGGATGCGAGGGAC CA C DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:127328588..127328683 26863196 MeRIP-seq:(Medium) rs1228747066 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_108908,RMVar_hsa_circ_350151,RMVar_hsa_circ_126800,RMVar_hsa_circ_119815,RMVar_hsa_circ_122922,RMVar_hsa_circ_119950,RMVar_hsa_circ_118430,RMVar_hsa_circ_119036,RMVar_hsa_circ_116315,RMVar_hsa_circ_83722,RMVar_hsa_circ_91893,RMVar_hsa_circ_99913,RMVar_hsa_circ_86451,RMVar_hsa_circ_75989,RMVar_hsa_circ_78072,RMVar_hsa_circ_81059,RMVar_hsa_circ_77938,RMVar_hsa_circ_66778,RMVar_hsa_circ_75684,RMVar_hsa_circ_147072,RMVar_hsa_circ_147076,RMVar_hsa_circ_147078,RMVar_hsa_circ_147077,RMVar_hsa_circ_147074,RMVar_hsa_circ_147075,RMVar_hsa_circ_147073,RMVar_hsa_circ_147064,RMVar_hsa_circ_147068,RMVar_hsa_circ_147070,RMVar_hsa_circ_147071,RMVar_hsa_circ_147069,RMVar_hsa_circ_147066,RMVar_hsa_circ_147067,RMVar_hsa_circ_147065,RMVar_hsa_circ_147062,RMVar_hsa_circ_147063,RMVar_hsa_circ_147061,RMVar_hsa_circ_83966,RMVar_hsa_circ_100948,RMVar_hsa_circ_147119,RMVar_hsa_circ_147120,RMVar_hsa_circ_113319,RMVar_hsa_circ_147129,RMVar_hsa_circ_78381,RMVar_hsa_circ_147146,RMVar_hsa_circ_3297,RMVar_hsa_circ_125308,RMVar_hsa_circ_126031,RMVar_hsa_circ_104942,RMVar_hsa_circ_122049,RMVar_hsa_circ_103655,RMVar_hsa_circ_147158,RMVar_hsa_circ_147160,RMVar_hsa_circ_147161,RMVar_hsa_circ_147159,RMVar_hsa_circ_147163,RMVar_hsa_circ_120566,RMVar_hsa_circ_123425,RMVar_hsa_circ_120099,RMVar_hsa_circ_147165,RMVar_hsa_circ_96471,RMVar_hsa_circ_147166,RMVar_hsa_circ_147164,RMVar_hsa_circ_147162,RMVar_hsa_circ_147173,RMVar_hsa_circ_111483,RMVar_hsa_circ_352329,RMVar_hsa_circ_369473,RMVar_hsa_circ_147178 68223 RMVar_ID_68223 Human_SNP_ID_451063463 m1A Human chr10 - 127428747 127428747 127428747 CACCACAGTCCACACGGTACCCCAATCCACACAGCACCCCAATCCACAGGACACCACAATCCACA CACCACAGTCCACACGGTACCCCAATCCACACGGCACCCCAATCCACAGGACACCACAATCCACA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:127428739..127428868 26863196 MeRIP-seq:(Medium) rs1308935771 Functional Loss SNV dbSNP153 33..33 33 - - - 68224 RMVar_ID_68224 Human_SNP_ID_451063590 m1A Human chr10 + 127428963 127428954 127428964 GATTGTGCCGTGTGGATTGGGGTGCTGTGTGGATTCGGGTACCATGTGGATTGGGGTGCCGTGTG GATTGTGCCGTGTGGATTGGGGTG__________TCGGGTACCATGTGGATTGGGGTGCCGTGTG GCTGTGTGGAT G DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:127428961..127429045 26863196 MeRIP-seq:(Medium) rs1459197651 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_5281180,Human_RBP_ID_23112868,Human_RBP_ID_24362793 RMVar_hsa_circ_126800,RMVar_hsa_circ_119815,RMVar_hsa_circ_86451,RMVar_hsa_circ_147076,RMVar_hsa_circ_147078,RMVar_hsa_circ_147077,RMVar_hsa_circ_125308,RMVar_hsa_circ_104942,RMVar_hsa_circ_147161,RMVar_hsa_circ_147163,RMVar_hsa_circ_96471,RMVar_hsa_circ_147162,RMVar_hsa_circ_6899,RMVar_hsa_circ_288062,RMVar_hsa_circ_147184,RMVar_hsa_circ_63057,RMVar_hsa_circ_46715 68225 RMVar_ID_68225 Human_SNP_ID_451238926 m1A Human chr10 - 128098095 128098095 128098095 CTGTCCTCTCTGTGTTCCCCAAATCAGAGAATAGCCCGCCATCCCCCAGGTCACCTGTCTGGATT CTGTCCTCTCTGTGTTCCCCAAATCAGAGAATCGCCCGCCATCCCCCAGGTCACCTGTCTGGATT T G MKI67 Ensembl:ENSG00000148773 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:128098050..128098275 26863196 MeRIP-seq:(Medium) rs1351327526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747497,Human_RBP_ID_1064750,Human_RBP_ID_4140094,Human_RBP_ID_5110089,Human_RBP_ID_5138430,Human_RBP_ID_8329454,Human_RBP_ID_9360961,Human_RBP_ID_17229866,Human_RBP_ID_17648346,Human_RBP_ID_17772876,Human_RBP_ID_18590004,Human_RBP_ID_18931326,Human_RBP_ID_21881938,Human_RBP_ID_26399399 Human_miRNA_ID_2653284,Human_miRNA_ID_2754482 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192 68226 RMVar_ID_68226 Human_SNP_ID_451239746 m1A Human chr10 - 128101387 128101387 128101387 CTCATGCAGAATCAGAAAGGGAAAGGAGAAGCAGGAAATTCAGACTCCATGTGCCTGAGATCAAG CTCATGCAGAATCAGAAAGGGAAAGGAGAAGCGGGAAATTCAGACTCCATGTGCCTGAGATCAAG T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:128101260..128101496;chr10:128101251..128101488;chr10:128101251..128101498 26863196 MeRIP-seq:(Medium) rs745966187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373760,Human_RBP_ID_982210,Human_RBP_ID_1762945,Human_RBP_ID_4112425,Human_RBP_ID_5946229,Human_RBP_ID_8759232,Human_RBP_ID_18188008,Human_RBP_ID_18590041,Human_RBP_ID_24550763,Human_RBP_ID_26595277 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_147197,RMVar_hsa_circ_85020,RMVar_hsa_circ_147196 68227 RMVar_ID_68227 Human_SNP_ID_451240138 m1A Human chr10 - 128102812 128102812 128102812 GAGGTGGCAAAGATGGAAGCGTCACGGGAACCAAGAGGCTGCGCTGCATGCCAGCACCAGAGGAA GAGGTGGCAAAGATGGAAGCGTCACGGGAACCGAGAGGCTGCGCTGCATGCCAGCACCAGAGGAA T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128102769..128102874 26863196 MeRIP-seq:(Medium) rs370598785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1762954,Human_RBP_ID_3343663,Human_RBP_ID_4140133,Human_RBP_ID_5946243,Human_RBP_ID_8759253,Human_RBP_ID_22879217 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68228 RMVar_ID_68228 Human_SNP_ID_451240139 m1A Human chr10 - 128102812 128102812 128102812 GAGGTGGCAAAGATGGAAGCGTCACGGGAACCAAGAGGCTGCGCTGCATGCCAGCACCAGAGGAA GAGGTGGCAAAGATGGAAGCGTCACGGGAACCCAGAGGCTGCGCTGCATGCCAGCACCAGAGGAA T G MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128102769..128102874 26863196 MeRIP-seq:(Medium) rs370598785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1762954,Human_RBP_ID_3343663,Human_RBP_ID_4140133,Human_RBP_ID_5946243,Human_RBP_ID_8759253,Human_RBP_ID_22879217 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68229 RMVar_ID_68229 Human_SNP_ID_451240332 m1A Human chr10 - 128103282 128103281 128103282 CAGGACACGTGCCCAGAAAGTAGAAGTGAAGGAGGAGCTGTTAGCAGTTGGCAAGCTCACACAAA CAGGACACGTGCCCAGAAAGTAGAAGTGAAGG_GGAGCTGTTAGCAGTTGGCAAGCTCACACAAA CT C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:128103233..128103398 26863196 MeRIP-seq:(Medium) rs367883634 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_862031,Human_RBP_ID_5946247,Human_RBP_ID_8759267,Human_RBP_ID_9360973,Human_RBP_ID_11308585,Human_RBP_ID_18158859,Human_RBP_ID_18239456,Human_RBP_ID_18410354,Human_RBP_ID_18590056,Human_RBP_ID_21999855,Human_RBP_ID_24542060,Human_RBP_ID_26316822 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68230 RMVar_ID_68230 Human_SNP_ID_451240684 m1A Human chr10 + 128104107 128104107 128104107 GAGATTTGCAGGGAATTTTTGTGTTTTTGTCAATAGTCATTGACTCTTCAGTGTGACCTGGTGCT GAGATTTGCAGGGAATTTTTGTGTTTTTGTCAGTAGTCATTGACTCTTCAGTGTGACCTGGTGCT A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:128104101..128104125 26863196 MeRIP-seq:(Medium) rs1228719840 Functional Loss SNV dbSNP153 33..33 33 - - - 68231 RMVar_ID_68231 Human_SNP_ID_451240730 m1A Human chr10 - 128104228 128104228 128104228 AGTCTCCAAAGCAGATCCTGGACCCAGCAGCAAGTGTAACTGGTAGCAGGAGGCAGCTGAGAACT AGTCTCCAAAGCAGATCCTGGACCCAGCAGCACGTGTAACTGGTAGCAGGAGGCAGCTGAGAACT T G MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128104178..128104332 26863196 MeRIP-seq:(Medium) rs1214671120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373765,Human_RBP_ID_747499,Human_RBP_ID_1443747,Human_RBP_ID_1762973,Human_RBP_ID_5946260,Human_RBP_ID_8759289,Human_RBP_ID_9360978,Human_RBP_ID_11308591,Human_RBP_ID_17458632,Human_RBP_ID_22708159,Human_RBP_ID_26316830,Human_RBP_ID_26876802,Human_RBP_ID_27571675,Human_RBP_ID_27802442 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68232 RMVar_ID_68232 Human_SNP_ID_451240941 m1A Human chr10 - 128104715 128104715 128104715 AGGAAAGCAGACGTAGAGGAAGAATTTTTAGCACTCAGGAAACGAACACCATCAGCAGGCAAAGC AGGAAAGCAGACGTAGAGGAAGAATTTTTAGCCCTCAGGAAACGAACACCATCAGCAGGCAAAGC T G MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128104664..128104822 26863196 MeRIP-seq:(Medium) rs747481200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2320,Human_RBP_ID_27558,Human_RBP_ID_1443760,Human_RBP_ID_1762982,Human_RBP_ID_2198348,Human_RBP_ID_8759306,Human_RBP_ID_9360983,Human_RBP_ID_11308598,Human_RBP_ID_26316834,Human_RBP_ID_27802445 Human_miRNA_ID_1092394 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68233 RMVar_ID_68233 Human_SNP_ID_451240948 m1A Human chr10 + 128104734 128104734 128104734 TTCGTTTCCTGAGTGCTAAAAATTCTTCCTCTACGTCTGCTTTCCTGAGGTTTCTCTTGGGCCGT TTCGTTTCCTGAGTGCTAAAAATTCTTCCTCTGCGTCTGCTTTCCTGAGGTTTCTCTTGGGCCGT A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:128104683..128104807 26863196 MeRIP-seq:(Medium) rs796052184 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_276 68234 RMVar_ID_68234 Human_SNP_ID_451241623 m1A Human chr10 - 128106205 128106205 128106205 ACACCCCAACAAACACAAAGCAACGGCCCAAGAGAAGCCTCAAGAAAGCAGACGTAGAGGAAGAA ACACCCCAACAAACACAAAGCAACGGCCCAAGGGAAGCCTCAAGAAAGCAGACGTAGAGGAAGAA T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:128106155..128106250 26863196 MeRIP-seq:(Medium) rs763372252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26876844 Human_miRNA_ID_2865559,Human_miRNA_ID_3117652 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68235 RMVar_ID_68235 Human_SNP_ID_451242156 m1A Human chr10 - 128107390 128107390 128107390 TCTTCCAGACACCAGTATGCACTGACAAGCCCACGACTCACGAGAAAACTACCAAAATAGCCTGC TCTTCCAGACACCAGTATGCACTGACAAGCCCGCGACTCACGAGAAAACTACCAAAATAGCCTGC T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128107341..128107679 26863196 MeRIP-seq:(Medium) rs199593811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1443808,Human_RBP_ID_2198404,Human_RBP_ID_8759384,Human_RBP_ID_17458666 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68236 RMVar_ID_68236 Human_SNP_ID_451242390 m1A Human chr10 - 128108036 128108036 128108036 CCAGTGGACACCCCAACAAGCACAAAGCAACGACCCAAGAGAAGTATCAGGAAAGCAGATGTAGA CCAGTGGACACCCCAACAAGCACAAAGCAACGGCCCAAGAGAAGTATCAGGAAAGCAGATGTAGA T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128107987..128108072 26863196 MeRIP-seq:(Medium) rs1437506182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27579,Human_RBP_ID_1763019,Human_RBP_ID_9321076,Human_RBP_ID_18410433,Human_RBP_ID_24542069,Human_RBP_ID_26876877 Human_miRNA_ID_3117655 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68237 RMVar_ID_68237 Human_SNP_ID_451242637 m1A Human chr10 - 128108652 128108652 128108652 GCACACGCACAGAGAGCCAGCAGGAGATGGCAAGAGCATCAGAACGTTTAAGGAGTCTCCAAAGC GCACACGCACAGAGAGCCAGCAGGAGATGGCAGGAGCATCAGAACGTTTAAGGAGTCTCCAAAGC T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128108603..128108773 26863196 MeRIP-seq:(Medium) rs186582207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1763029,Human_RBP_ID_5946318,Human_RBP_ID_11308661,Human_RBP_ID_24542072 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68238 RMVar_ID_68238 Human_SNP_ID_451242654 m1A Human chr10 - 128108680 128108680 128108680 AGTTCACACGGACGTCAGGGGAGACCACGCACACGCACAGAGAGCCAGCAGGAGATGGCAAGAGC AGTTCACACGGACGTCAGGGGAGACCACGCACGCGCACAGAGAGCCAGCAGGAGATGGCAAGAGC T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:128108629..128108796 26863196 MeRIP-seq:(Medium) rs746108417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2324,Human_RBP_ID_5946319,Human_RBP_ID_24542072 Human_miRNA_ID_1092403,Human_miRNA_ID_2083399,Human_miRNA_ID_2205918,Human_miRNA_ID_2512021,Human_miRNA_ID_3054837 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 68239 RMVar_ID_68239 Human_SNP_ID_451242790 m1A Human chr10 + 128109028 128109028 128109028 CATTGCTTTCATCTTTTCATCGTTTTCTTTTAATTCAATATTTTCCTTATATGTCTCAAAAGGTC CATTGCTTTCATCTTTTCATCGTTTTCTTTTAGTTCAATATTTTCCTTATATGTCTCAAAAGGTC A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:128108981..128109121 26863196 MeRIP-seq:(Medium) rs1313231103 Functional Loss SNV dbSNP153 33..33 33 - - - 68240 RMVar_ID_68240 Human_SNP_ID_451243708 m1A Human chr10 - 128112192 128112190 128112193 AAAGAGAGTGTCTATCAGCCGAAGTCAACATGATATTTTACAGATGATATGTTCCAAAAGAAGAA AAAGAGAGTGTCTATCAGCCGAAGTCAACAT___ATTTTACAGATGATATGTTCCAAAAGAAGAA TATC T MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:128111951..128112239 32194978 MeRIP-seq:(Medium) rs1490860186 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_27587,Human_RBP_ID_982262,Human_RBP_ID_1763057,Human_RBP_ID_3343702,Human_RBP_ID_8985230,Human_RBP_ID_17648102,Human_RBP_ID_17786911,Human_RBP_ID_26876921,Human_RBP_ID_27803133 Human_Splice_Rec_1188459,Human_Splice_Rec_1188487,Human_Splice_Rec_1188501 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_9264,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147197 68241 RMVar_ID_68241 Human_SNP_ID_451247286 m1A Human chr10 + 128125673 128125673 128125673 AGTAACCAGGCGTCTCGTGGGCCACATTTTCTAAACAGTAAGTTGAGTATAATCCGTAGGGGAAG AGTAACCAGGCGTCTCGTGGGCCACATTTTCTCAACAGTAAGTTGAGTATAATCCGTAGGGGAAG A C lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:128125625..128125769 26863196 MeRIP-seq:(Medium) rs763373863 Functional Loss SNV dbSNP153 33..33 33 - - - 68242 RMVar_ID_68242 Human_SNP_ID_451247287 m1A Human chr10 + 128125673 128125673 128125673 AGTAACCAGGCGTCTCGTGGGCCACATTTTCTAAACAGTAAGTTGAGTATAATCCGTAGGGGAAG AGTAACCAGGCGTCTCGTGGGCCACATTTTCTGAACAGTAAGTTGAGTATAATCCGTAGGGGAAG A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:128125625..128125769 26863196 MeRIP-seq:(Medium) rs763373863 Functional Loss SNV dbSNP153 33..33 33 - - - 68243 RMVar_ID_68243 Human_SNP_ID_451247437 m1A Human chr10 + 128126172 128126172 128126172 CTCGTCAAGTCGCACCCAAAGTCCGCCGCAGGAGGAGCCGGCGCCGCGCTCACCTCCGCCCGGTA CTCGTCAAGTCGCACCCAAAGTCCGCCGCAGGGGGAGCCGGCGCCGCGCTCACCTCCGCCCGGTA A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:128126076..128126400 26863196 MeRIP-seq:(Medium) rs943978847 Functional Loss SNV dbSNP153 33..33 33 - - - 68244 RMVar_ID_68244 Human_SNP_ID_451247508 m1A Human chr10 + 128126354 128126354 128126354 CCTACAGGCTACGTCCCCGGGCGCCCGGCTCTAGCGGCTCCCACCGAGTCGAGTCCTCCCGCCCG CCTACAGGCTACGTCCCCGGGCGCCCGGCTCTGGCGGCTCCCACCGAGTCGAGTCCTCCCGCCCG A G lnc-PTPRE-3 RNACentral:URS00008BEDDC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:128126110..128126425;chr10:128126076..128126425;chr10:128126073..128126450;chr10:128126070..128126450 26863196 MeRIP-seq:(Medium) rs1227471347 Functional Loss SNV dbSNP153 33..33 33 - - - 68245 RMVar_ID_68245 Human_SNP_ID_451247516 m1A Human chr10 - 128126370 128126370 128126370 GCTGCGGGCGGGCGGGCGGGCGGGAGGACTCGACTCGGTGGGAGCCGCTAGAGCCGGGCGCCCGG GCTGCGGGCGGGCGGGCGGGCGGGAGGACTCGTCTCGGTGGGAGCCGCTAGAGCCGGGCGCCCGG T A MKI67 Ensembl:ENSG00000148773 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:128126151..128126400 26863196 MeRIP-seq:(Medium) rs1299972527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225840,Human_RBP_ID_861431,Human_RBP_ID_4136101,Human_RBP_ID_5138433,Human_RBP_ID_5313381,Human_RBP_ID_5414948,Human_RBP_ID_8765515,Human_RBP_ID_9274313,Human_RBP_ID_9320761,Human_RBP_ID_9361015,Human_RBP_ID_18416203,Human_RBP_ID_22432292,Human_RBP_ID_24362797,Human_RBP_ID_26316008,Human_RBP_ID_26767824,Human_RBP_ID_27802463 68246 RMVar_ID_68246 Human_SNP_ID_451615918 m1A Human chr10 - 129536218 129536218 129536218 TTCCAAGTACCTAAACAGAAATAATTTTTAAGACAAAGTGTATAGGTAAGAGGCTGGTCGTATAT TTCCAAGTACCTAAACAGAAATAATTTTTAAGGCAAAGTGTATAGGTAAGAGGCTGGTCGTATAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:129536215..129536304 26863196 MeRIP-seq:(Medium) rs764896052 Functional Loss SNV dbSNP153 33..33 33 - - - 68247 RMVar_ID_68247 Human_SNP_ID_451768981 m1A Human chr10 - 130110104 130110104 130110104 TGCGTGGGTAAGTCAGGTATGTGTGAGACTTGAAGGATGACCGGGGGTAGGCAGGATGGGAGGTG TGCGTGGGTAAGTCAGGTATGTGTGAGACTTGGAGGATGACCGGGGGTAGGCAGGATGGGAGGTG T C C10orf143 Ensembl:ENSG00000237489 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:130110054..130110145 26863196 MeRIP-seq:(Medium) rs182711592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5163407,Human_RBP_ID_5946794,Human_RBP_ID_11309343,Human_RBP_ID_23444089 68248 RMVar_ID_68248 Human_SNP_ID_451769477 m1A Human chr10 + 130111401 130111401 130111401 GTGGCTGGTGGCTGCTGGTTGGGAGGCCCCGGAAGGACTTCTACTCCTCCGTAGGCTGGAGGGCA GTGGCTGGTGGCTGCTGGTTGGGAGGCCCCGGGAGGACTTCTACTCCTCCGTAGGCTGGAGGGCA A G lnc-GLRX3-2,lnc-GLRX3-2:2,lnc-GLRX3-2:3,lnc-GLRX3-2:4 RNACentral:URS0000D5BC4F,RNACentral:URS00008B1FFC,RNACentral:URS0000D5DD7F,RNACentral:URS00008B30A2 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:130111351..130111423 26863196 MeRIP-seq:(Medium) rs1242375144 Functional Loss SNV dbSNP153 33..33 33 - - - 68249 RMVar_ID_68249 Human_SNP_ID_451778600 m1A Human chr10 - 130145276 130145276 130145276 AAACTTGAGGGAGTTCTTTAGCTAACTCTGCCATAACTTCGTTCATCTGTGCACACTGTGGAGCC AAACTTGAGGGAGTTCTTTAGCTAACTCTGCCGTAACTTCGTTCATCTGTGCACACTGTGGAGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:130145226..130145300 26863196 MeRIP-seq:(Medium) rs750613292 Functional Loss SNV dbSNP153 33..33 33 - - - 68250 RMVar_ID_68250 Human_SNP_ID_451781304 m1A Human chr10 + 130155643 130155643 130155643 GTGGGAGGAGCAGGTTTAGTGAGAGGTGTTTGATAGAGCTCTGAGTGCAGGTGTTGAGTGTATAG GTGGGAGGAGCAGGTTTAGTGAGAGGTGTTTGGTAGAGCTCTGAGTGCAGGTGTTGAGTGTATAG A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:130155613..130156006 26863196 MeRIP-seq:(Medium) rs572705317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11309815,Human_RBP_ID_23444158,Human_RBP_ID_27605074 RMVar_hsa_circ_70203,RMVar_hsa_circ_301355,RMVar_hsa_circ_79780,RMVar_hsa_circ_323123,RMVar_hsa_circ_147211,RMVar_hsa_circ_371748,RMVar_hsa_circ_314319,RMVar_hsa_circ_288421,RMVar_hsa_circ_291591,RMVar_hsa_circ_97963,RMVar_hsa_circ_147213,RMVar_hsa_circ_147215,RMVar_hsa_circ_55682,RMVar_hsa_circ_147214,RMVar_hsa_circ_147212 68251 RMVar_ID_68251 Human_SNP_ID_451781831 m1A Human chr10 - 130157526 130157526 130157526 GTAGACTGAGTAAGGAAGATCCATTCTCACCCAATATGGGCGGGGGGGGGGGGGGGGGGGGGGGG GTAGACTGAGTAAGGAAGATCCATTCTCACCCGATATGGGCGGGGGGGGGGGGGGGGGGGGGGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:130157484..130157612 26863196 MeRIP-seq:(Medium) rs1011471968 Functional Loss SNV dbSNP153 33..33 33 - - - 68252 RMVar_ID_68252 Human_SNP_ID_451792011 m1A Human chr10 - 130195391 130195391 130195391 CCTCTGTCCCCAGGCCAGCAGCCACCACCCACATAGCCTGCCTGCACCTGGGTTTCCGGCCGTGC CCTCTGTCCCCAGGCCAGCAGCCACCACCCACGTAGCCTGCCTGCACCTGGGTTTCCGGCCGTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:130195341..130195448 26863196 MeRIP-seq:(Medium) rs1431010722 Functional Loss SNV dbSNP153 33..33 33 - - - 68253 RMVar_ID_68253 Human_SNP_ID_451793973 m1A Human chr10 + 130201608 130201588 130201608 AAGAGGGGGACATGGAGGTGAGGAGGGACCTGAGGAGGTGAGGAGGGATCTGAGGAAGTGAGGGG AAGAGGGGGACAT____________________GGAGGTGAGGAGGGATCTGAGGAAGTGAGGGG TGGAGGTGAGGAGGGACCTGA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:130201558..130201801 26863196 MeRIP-seq:(Medium) rs1259379221 Functional Loss DEL dbSNP153 14..33 33 - - - 68254 RMVar_ID_68254 Human_SNP_ID_451794018 m1A Human chr10 + 130201711 130201711 130201711 AGAGATCTGAGGAGGTCAGGAAAGATCTGAGGAGGTTAGGAGGGATCTTAGGACGTGAGGAGAGA AGAGATCTGAGGAGGTCAGGAAAGATCTGAGGGGGTTAGGAGGGATCTTAGGACGTGAGGAGAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:130201296..130201819;chr10:130201262..130201865 26863196 MeRIP-seq:(Medium) rs1251909440 Functional Loss SNV dbSNP153 33..33 33 - - - 68255 RMVar_ID_68255 Human_SNP_ID_451794188 m1A Human chr10 - 130202098 130202098 130202098 CTCCTCAGATCCCTCCTCACCTCCTCAGATCCACCCTCTCCTCCTCAAATTCACCCTCACCTCCC CTCCTCAGATCCCTCCTCACCTCCTCAGATCCCCCCTCTCCTCCTCAAATTCACCCTCACCTCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:130202065..130202282 26863196 MeRIP-seq:(Medium) rs1408788632 Functional Loss SNV dbSNP153 33..33 33 - - - 68256 RMVar_ID_68256 Human_SNP_ID_451796078 m1A Human chr10 + 130207554 130207533 130207555 ACACTCACACGTCACACACACCAATCTCATACACCACACACACCACACCCCCACACAATCTCACA ACACTCACACGT______________________CACACACACCACACCCCCACACAATCTCACA TCACACACACCAATCTCATACAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:130207537..130207602 26863196 MeRIP-seq:(Medium) rs1565011195 Functional Loss DEL dbSNP153 13..34 33 - - - Human_RBP_ID_2198897 68257 RMVar_ID_68257 Human_SNP_ID_451796087 m1A Human chr10 + 130207554 130207552 130207555 ACACTCACACGTCACACACACCAATCTCATACACCACACACACCACACCCCCACACAATCTCACA ACACTCACACGTCACACACACCAATCTCATA___CACACACACCACACCCCCACACAATCTCACA ACAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:130207537..130207602 26863196 MeRIP-seq:(Medium) rs796964185 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2198897 68258 RMVar_ID_68258 Human_SNP_ID_452031716 m1A Human chr10 - 131085716 131085716 131085716 AGAGTGAGGGGGACAGACAAGTCCTGAGGTTGAGCTGGGGGAACTCAGGAGCAGAGCCTTCCAGG AGAGTGAGGGGGACAGACAAGTCCTGAGGTTGGGCTGGGGGAACTCAGGAGCAGAGCCTTCCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131085686..131085764 26863196 MeRIP-seq:(Medium) rs1429053906 Functional Loss SNV dbSNP153 33..33 33 - - - 68259 RMVar_ID_68259 Human_SNP_ID_452256444 m1A Human chr10 + 131916787 131916755 131916787 GGGTGGAATGACACAGTGTAGGGACCTCACGCAGGTGGAATGACACAGTGTTTGTAGGGACCTCA G________________________________GGTGGAATGACACAGTGTTTGTAGGGACCTCA GGGTGGAATGACACAGTGTAGGGACCTCACGCA G PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:131916779..131916929 26863196 MeRIP-seq:(Medium) rs1348175064 Functional Loss DEL dbSNP153 2..33 33 - - - 68260 RMVar_ID_68260 Human_SNP_ID_452256466 m1A Human chr10 + 131916787 131916787 131916787 GGGTGGAATGACACAGTGTAGGGACCTCACGCAGGTGGAATGACACAGTGTTTGTAGGGACCTCA GGGTGGAATGACACAGTGTAGGGACCTCACGCGGGTGGAATGACACAGTGTTTGTAGGGACCTCA A G PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:131916779..131916929 26863196 MeRIP-seq:(Medium) rs376559718 Functional Loss SNV dbSNP153 33..33 33 - - - 68261 RMVar_ID_68261 Human_SNP_ID_452256735 m1A Human chr10 + 131917294 131917294 131917294 CAGGCGGGTGGAATGACACAGTGTTTGTAGGGACCTCAGGCAGGTGGAATGACACAGTGTAGGGA CAGGCGGGTGGAATGACACAGTGTTTGTAGGGTCCTCAGGCAGGTGGAATGACACAGTGTAGGGA A T PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131917291..131917534 26863196 MeRIP-seq:(Medium) rs367866132 Functional Loss SNV dbSNP153 33..33 33 - - - 68262 RMVar_ID_68262 Human_SNP_ID_452256744 m1A Human chr10 + 131917309 131917309 131917309 ACACAGTGTTTGTAGGGACCTCAGGCAGGTGGAATGACACAGTGTAGGGACCTCAGGCGGGTGGG ACACAGTGTTTGTAGGGACCTCAGGCAGGTGGGATGACACAGTGTAGGGACCTCAGGCGGGTGGG A G PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:131917307..131917466 26863196 MeRIP-seq:(Medium) rs1404978036 Functional Loss SNV dbSNP153 33..33 33 - - - 68263 RMVar_ID_68263 Human_SNP_ID_452256929 m1A Human chr10 - 131917674 131917674 131917674 CCACCCGCCTGAGGTCCCTACACTGTCATTCCACCCACATGAGGTCCCTACACTGTGTCATTCCA CCACCCGCCTGAGGTCCCTACACTGTCATTCCTCCCACATGAGGTCCCTACACTGTGTCATTCCA T A lnc-BNIP3-1,lnc-BNIP3-1:2 RNACentral:URS00009BEB97,RNACentral:URS00008B94C7 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:131917658..131917742 26863196 MeRIP-seq:(Medium) rs1341722282 Functional Loss SNV dbSNP153 33..33 33 - - - 68264 RMVar_ID_68264 Human_SNP_ID_452257090 m1A Human chr10 - 131918023 131918023 131918023 ACACTGTGTCATCCCACCCGCCTGAGGTCCCTACACTGTGTCATTCCACCCACGTGAGGTCCCTG ACACTGTGTCATCCCACCCGCCTGAGGTCCCTGCACTGTGTCATTCCACCCACGTGAGGTCCCTG T C lnc-BNIP3-1,lnc-BNIP3-1:2 RNACentral:URS00009BEB97,RNACentral:URS00008B94C7 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131918017..131918144 26863196 MeRIP-seq:(Medium) rs1262152244 Functional Loss SNV dbSNP153 33..33 33 - - - 68265 RMVar_ID_68265 Human_SNP_ID_452257098 m1A Human chr10 + 131918033 131918033 131918033 ACGTGGGTGGAATGACACAGTGTAGGGACCTCAGGCGGGTGGGATGACACAGTGTTTGTAGGGAC ACGTGGGTGGAATGACACAGTGTAGGGACCTCCGGCGGGTGGGATGACACAGTGTTTGTAGGGAC A C PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:131918027..131918145;chr10:131918027..131918151 26863196 MeRIP-seq:(Medium) rs1272667090 Functional Loss SNV dbSNP153 33..33 33 - - - 68266 RMVar_ID_68266 Human_SNP_ID_452257492 m1A Human chr10 - 131918804 131918804 131918804 ACCCCCGTGAGGTCCCCACACTGTGTCATTCCACCCGCGTGAGGTCCCTACAAACACTGTGTCAT ACCCCCGTGAGGTCCCCACACTGTGTCATTCCGCCCGCGTGAGGTCCCTACAAACACTGTGTCAT T C lnc-BNIP3-1,lnc-BNIP3-1:2 RNACentral:URS00009BEB97,RNACentral:URS00008B94C7 lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:131918801..131919234 26863196 MeRIP-seq:(Medium) rs1554893688 Functional Loss SNV dbSNP153 33..33 33 - - - 68267 RMVar_ID_68267 Human_SNP_ID_452257496 m1A Human chr10 + 131918815 131918814 131918816 TTTGTAGGGACCTCACGCGGGTGGAATGACACAGTGTGGGGACCTCACGGGGGTGGAATGACACA TTTGTAGGGACCTCACGCGGGTGGAATGACAC__TGTGGGGACCTCACGGGGGTGGAATGACACA CAG C PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131918812..131918953 26863196 MeRIP-seq:(Medium) rs1412238688 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2085,Human_RBP_ID_5234825 68268 RMVar_ID_68268 Human_SNP_ID_452257497 m1A Human chr10 + 131918815 131918815 131918815 TTTGTAGGGACCTCACGCGGGTGGAATGACACAGTGTGGGGACCTCACGGGGGTGGAATGACACA TTTGTAGGGACCTCACGCGGGTGGAATGACACCGTGTGGGGACCTCACGGGGGTGGAATGACACA A C PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131918812..131918953 26863196 MeRIP-seq:(Medium) rs554000529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2085,Human_RBP_ID_5234825 68269 RMVar_ID_68269 Human_SNP_ID_452257595 m1A Human chr10 - 131919020 131919016 131919020 CTGTGTCATCCCGCTCGCCTGAGGTCCCTACAAACACTGTGTCATTCCACCCGCCTGAGGTCCCT CTGTGTCATCCCGCTCGCCTGAGGTCCCTACA____CTGTGTCATTCCACCCGCCTGAGGTCCCT GTGTT G lnc-BNIP3-1,lnc-BNIP3-1:2 RNACentral:URS00009BEB97,RNACentral:URS00008B94C7 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:131919009..131919101 26863196 MeRIP-seq:(Medium) rs1311151013 Functional Loss DEL dbSNP153 33..36 33 - - - 68270 RMVar_ID_68270 Human_SNP_ID_452260108 m1A Human chr10 - 131927183 131927183 131927183 TCACACCTCTCCTCTCCCCTCAAACTTCCAGCACCCCAGCCACTCACCCCACTTCCCATTAATGA TCACACCTCTCCTCTCCCCTCAAACTTCCAGCCCCCCAGCCACTCACCCCACTTCCCATTAATGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:131927178..131927512 26863196 MeRIP-seq:(Medium) rs1554895057 Functional Loss SNV dbSNP153 33..33 33 - - - 68271 RMVar_ID_68271 Human_SNP_ID_452276042 m1A Human chr10 - 131981763 131981763 131981763 CGGAGCGCCCGGGATGCAGGAGGAGAGCCTGCAGGGTGAGGCGGAGGAGGCGGCGCGGGAGCCGA CGGAGCGCCCGGGATGCAGGAGGAGAGCCTGCCGGGTGAGGCGGAGGAGGCGGCGCGGGAGCCGA T G BNIP3 Ensembl:ENSG00000176171 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:131981761..131981900 26863196 MeRIP-seq:(Medium) rs969641244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748231,Human_RBP_ID_863040,Human_RBP_ID_4136106,Human_RBP_ID_5313133,Human_RBP_ID_17345811,Human_RBP_ID_18971425,Human_RBP_ID_19045992,Human_RBP_ID_22431897 Human_Splice_Rec_1189013,Human_Splice_Rec_1189023,Human_Splice_Rec_1189031,Human_Splice_Rec_1189041 68272 RMVar_ID_68272 Human_SNP_ID_452308847 m1A Human chr10 + 132104681 132104678 132104681 CCGCGGTGTGCTTTCCCCTCCAGGTGAATGAGAAGATGTAGTGTGACAGCAGCCCGGGTGACACC CCGCGGTGTGCTTTCCCCTCCAGGTGAATG___AGATGTAGTGTGACAGCAGCCCGGGTGACACC GAGA G JAKMIP3 Ensembl:ENSG00000188385 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132104664..132104787 26863196 MeRIP-seq:(Medium) rs1225736156 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_1189044,Human_Splice_Rec_1189090,Human_Splice_Rec_1189136,Human_Splice_Rec_1189178,Human_Splice_Rec_1189222,Human_Splice_Rec_1189268,Human_Splice_Rec_1189312,Human_Splice_Rec_1189356,Human_Splice_Rec_1189402,Human_Splice_Rec_1189578,Human_Splice_Rec_1189626,Human_Splice_Rec_1189670 RMVar_hsa_circ_2008,RMVar_hsa_circ_307328,RMVar_hsa_circ_147255 68273 RMVar_ID_68273 Human_SNP_ID_452308881 m1A Human chr10 + 132104760 132104760 132104760 CGTGGACACCCCAGCCACCCCCAGCCCAGCCCAGCCGGAGCACCCTACCCCTGGGCATCCCCCTG CGTGGACACCCCAGCCACCCCCAGCCCAGCCCTGCCGGAGCACCCTACCCCTGGGCATCCCCCTG A T JAKMIP3 Ensembl:ENSG00000188385 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132104639..132104840 26863196 MeRIP-seq:(Medium) rs1302140318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1189044,Human_Splice_Rec_1189090,Human_Splice_Rec_1189136,Human_Splice_Rec_1189178,Human_Splice_Rec_1189222,Human_Splice_Rec_1189268,Human_Splice_Rec_1189312,Human_Splice_Rec_1189356,Human_Splice_Rec_1189402,Human_Splice_Rec_1189578,Human_Splice_Rec_1189626,Human_Splice_Rec_1189670 RMVar_hsa_circ_2008,RMVar_hsa_circ_307328,RMVar_hsa_circ_147255 68274 RMVar_ID_68274 Human_SNP_ID_452350997 m1A Human chr10 - 132224460 132224460 132224460 TGGAGTCCCTGGTGCAGCTGTTCAGCACCGTGAGCGTCCAGTATGTCCCCACGTGGTCCAAGGAG TGGAGTCCCTGGTGCAGCTGTTCAGCACCGTGGGCGTCCAGTATGTCCCCACGTGGTCCAAGGAG T C STK32C Ensembl:ENSG00000165752 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:132224338..132224470 26863196 MeRIP-seq:(Medium) rs149249276 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1190022,Human_Splice_Rec_1190023,Human_Splice_Rec_1190046,Human_Splice_Rec_1190047,Human_Splice_Rec_1190068,Human_Splice_Rec_1190069 RMVar_hsa_circ_299201,RMVar_hsa_circ_332087 68275 RMVar_ID_68275 Human_SNP_ID_452368922 m1A Human chr10 - 132279692 132279672 132279693 TCAGGGAGTGGAGTGTCGTGATCACGGAGTGGAGTGTCGTGATCACGGAGTGCAGTGGCTTGATC TCAGGGAGTGGAGTGTCGTGATCACGGAGTG_____________________CAGTGGCTTGATC GCACTCCGTGATCACGACACTC G STK32C Ensembl:ENSG00000165752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132279686..132279751 26863196 MeRIP-seq:(Medium) rs1311886203 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_8985408 68276 RMVar_ID_68276 Human_SNP_ID_452369188 m1A Human chr10 - 132280172 132280172 132280172 ATGGTCATGGAGCGCAGGTGGCGTGGTCACGGAGTGCAGGGGCGTGATCACAGAGTGCAGGGGCG ATGGTCATGGAGCGCAGGTGGCGTGGTCACGGGGTGCAGGGGCGTGATCACAGAGTGCAGGGGCG T C STK32C Ensembl:ENSG00000165752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132280165..132280230 26863196 MeRIP-seq:(Medium) rs575302254 Functional Loss SNV dbSNP153 33..33 33 - - - 68277 RMVar_ID_68277 Human_SNP_ID_452369366 m1A Human chr10 - 132280470 132280463 132280471 CATGGAGCACAGGTGGCATGATCACGGAGTGCAGGGGCGTGATCATGGGGTGCAGTGGCGTGATC CATGGAGCACAGGTGGCATGATCACGGAGTG________TGATCATGGGGTGCAGTGGCGTGATC ACGCCCCTG A STK32C Ensembl:ENSG00000165752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132280468..132280637 26863196 MeRIP-seq:(Medium) rs1183978526 Functional Loss DEL dbSNP153 32..39 33 - - - 68278 RMVar_ID_68278 Human_SNP_ID_452369373 m1A Human chr10 - 132280470 132280470 132280470 CATGGAGCACAGGTGGCATGATCACGGAGTGCAGGGGCGTGATCATGGGGTGCAGTGGCGTGATC CATGGAGCACAGGTGGCATGATCACGGAGTGCCGGGGCGTGATCATGGGGTGCAGTGGCGTGATC T G STK32C Ensembl:ENSG00000165752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132280468..132280637 26863196 MeRIP-seq:(Medium) rs1402499222 Functional Loss SNV dbSNP153 33..33 33 - - - 68279 RMVar_ID_68279 Human_SNP_ID_452369609 m1A Human chr10 + 132280884 132280884 132280884 CTGAGGCCTCCATGCCGTGACCACGCCCCTGCACTCCGTGACCACGCCCCTGCATCCTGTGACCA CTGAGGCCTCCATGCCGTGACCACGCCCCTGCGCTCCGTGACCACGCCCCTGCATCCTGTGACCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132280842..132280941 26863196 MeRIP-seq:(Medium) rs1001299521 Functional Loss SNV dbSNP153 33..33 33 - - - 68280 RMVar_ID_68280 Human_SNP_ID_452374387 m1A Human chr10 + 132297341 132297341 132297341 GTGCCTCCGCCCCCGCTGCCAGCAGACCCCGAAGATCCACCGAAGGGCCTGCTGTGGCTGTGCCT GTGCCTCCGCCCCCGCTGCCAGCAGACCCCGAGGATCCACCGAAGGGCCTGCTGTGGCTGTGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132297338..132297477 26863196 MeRIP-seq:(Medium) rs777696661 Functional Loss SNV dbSNP153 33..33 33 - - - 68281 RMVar_ID_68281 Human_SNP_ID_452377332 m1A Human chr10 + 132307714 132307714 132307714 ACATCGCCCGAGTCCCGGGCCCGGGGCTGGCCAGCAGCGGGCGGCGGCAGGGCCGAGGGCGCGTC ACATCGCCCGAGTCCCGGGCCCGGGGCTGGCCGGCAGCGGGCGGCGGCAGGGCCGAGGGCGCGTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:132307713..132307844 26863196 MeRIP-seq:(Medium) rs1564796501 Functional Loss SNV dbSNP153 33..33 33 - - - 68282 RMVar_ID_68282 Human_SNP_ID_452383077 m1A Human chr10 - 132330401 132330401 132330401 CCGGGCAGAGCAAGGAGAGAATGAGGAGTGACATGGGTGTTGCCGTGAGTGGCGAAGGGGATGGA CCGGGCAGAGCAAGGAGAGAATGAGGAGTGACGTGGGTGTTGCCGTGAGTGGCGAAGGGGATGGA T C STK32C Ensembl:ENSG00000165752 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:132330351..132330485 26863196 MeRIP-seq:(Medium) rs1215865745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2199622,Human_RBP_ID_4140424,Human_RBP_ID_23304225,Human_RBP_ID_23445038 Human_Splice_Rec_1190086 68283 RMVar_ID_68283 Human_SNP_ID_452383656 m1A Human chr10 - 132331787 132331787 132331787 GGGTGGTGGTCGACGGGCAAGTAGAGACCGCGAGGGTCTGGAGGGGCGACCGGCCTGGCACAGAG GGGTGGTGGTCGACGGGCAAGTAGAGACCGCGGGGGTCTGGAGGGGCGACCGGCCTGGCACAGAG T C STK32C Ensembl:ENSG00000165752 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:132331376..132331900;chr10:132330326..132331862;chr10:132331597..132331867 26863196 MeRIP-seq:(Medium) rs1333267777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374152,Human_RBP_ID_3364990,Human_RBP_ID_4136579,Human_RBP_ID_18416410 68284 RMVar_ID_68284 Human_SNP_ID_452383666 m1A Human chr10 - 132331800 132331800 132331800 CGCGGCCTTGAAGGGGTGGTGGTCGACGGGCAAGTAGAGACCGCGAGGGTCTGGAGGGGCGACCG CGCGGCCTTGAAGGGGTGGTGGTCGACGGGCAGGTAGAGACCGCGAGGGTCTGGAGGGGCGACCG T C STK32C Ensembl:ENSG00000165752 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:132331595..132331850 26863196 MeRIP-seq:(Medium) rs774886587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364990,Human_RBP_ID_4136579,Human_RBP_ID_18416410,Human_RBP_ID_22151992 68285 RMVar_ID_68285 Human_SNP_ID_452387808 m1A Human chr10 + 132345790 132345790 132345790 AGGCACAGCCGGAGCCAGGACACAGGGAGCACAGGAGACACGGACAGACCCTGCTGGAGGATCAG AGGCACAGCCGGAGCCAGGACACAGGGAGCACGGGAGACACGGACAGACCCTGCTGGAGGATCAG A G LRRC27 Ensembl:ENSG00000148814 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132345646..132345942 26863196 MeRIP-seq:(Medium) rs7894664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351271,RMVar_hsa_circ_42924,RMVar_hsa_circ_301730,RMVar_hsa_circ_362393 68286 RMVar_ID_68286 Human_SNP_ID_452391823 m1A Human chr10 + 132358722 132358693 132358722 GCCGAGGTGGTAGAGCAGTGTGGGGAGGAGCCAAGGTGGTGGAGCAGCGTGGGGAGGAGCCGAGG GCCG_____________________________AGGTGGTGGAGCAGCGTGGGGAGGAGCCGAGG GAGGTGGTAGAGCAGTGTGGGGAGGAGCCA G LRRC27 Ensembl:ENSG00000148814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132358705..132358834 26863196 MeRIP-seq:(Medium) rs1564846264 Functional Loss DEL dbSNP153 5..33 33 - - - RMVar_hsa_circ_42924,RMVar_hsa_circ_301730,RMVar_hsa_circ_362393 68287 RMVar_ID_68287 Human_SNP_ID_452391841 m1A Human chr10 + 132358722 132358722 132358722 GCCGAGGTGGTAGAGCAGTGTGGGGAGGAGCCAAGGTGGTGGAGCAGCGTGGGGAGGAGCCGAGG GCCGAGGTGGTAGAGCAGTGTGGGGAGGAGCCGAGGTGGTGGAGCAGCGTGGGGAGGAGCCGAGG A G LRRC27 Ensembl:ENSG00000148814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132358705..132358834 26863196 MeRIP-seq:(Medium) rs189281170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42924,RMVar_hsa_circ_301730,RMVar_hsa_circ_362393 68288 RMVar_ID_68288 Human_SNP_ID_452392085 m1A Human chr10 + 132359152 132359149 132359152 TGGTGGAGCGTGGGAAGGAGCCGAGGTGGTGGAGCAGCGTGGGGAGGTGCTGAGGTGGTGGAGCG TGGTGGAGCGTGGGAAGGAGCCGAGGTGGT___GCAGCGTGGGGAGGTGCTGAGGTGGTGGAGCG TGGA T LRRC27 Ensembl:ENSG00000148814 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:132359047..132359192 26863196 MeRIP-seq:(Medium) rs1363435383 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_42924,RMVar_hsa_circ_301730,RMVar_hsa_circ_362393 68289 RMVar_ID_68289 Human_SNP_ID_452402750 m1A Human chr10 + 132392528 132392528 132392528 GTGATGGTGATGATGGTGATGTGATAATGGTGATGGTGATGGTAGTGGTGATGGGGGTGGTGGTA GTGATGGTGATGATGGTGATGTGATAATGGTGGTGGTGATGGTAGTGGTGATGGGGGTGGTGGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132392480..132392589 26863196 MeRIP-seq:(Medium) rs12359584 Functional Loss SNV dbSNP153 33..33 33 - - - 68290 RMVar_ID_68290 Human_SNP_ID_452403895 m1A Human chr10 - 132396253 132396253 132396253 CCTTCCCCCAGGCGCCCGGCTCCCGCGCCTTCAGGCGTCAAAGCCCCCGACTTCCCCGAGCACCA CCTTCCCCCAGGCGCCCGGCTCCCGCGCCTTCGGGCGTCAAAGCCCCCGACTTCCCCGAGCACCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:132396211..132396708 26863196 MeRIP-seq:(Medium) rs150152322 Functional Loss SNV dbSNP153 33..33 33 - - - 68291 RMVar_ID_68291 Human_SNP_ID_452408568 m1A Human chr10 + 132409851 132409848 132409851 GGCCTGGACTGGGATCCGGGAAGGCTTCCTGGAGGAGGTGGCAGGAGCCAGGATCTGAATGGTGA GGCCTGGACTGGGATCCGGGAAGGCTTCCT___GGAGGTGGCAGGAGCCAGGATCTGAATGGTGA TGGA T PWWP2B Ensembl:ENSG00000171813 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132409819..132409976 26863196 MeRIP-seq:(Medium) rs536488592 Functional Loss DEL dbSNP153 31..33 33 - - - 68292 RMVar_ID_68292 Human_SNP_ID_452408573 m1A Human chr10 + 132409876 132409876 132409876 TTCCTGGAGGAGGTGGCAGGAGCCAGGATCTGAATGGTGAGCTAATCAGGAGCTGATGGGGTGAG TTCCTGGAGGAGGTGGCAGGAGCCAGGATCTGGATGGTGAGCTAATCAGGAGCTGATGGGGTGAG A G PWWP2B Ensembl:ENSG00000171813 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132409826..132410017 26863196 MeRIP-seq:(Medium) rs914099384 Functional Loss SNV dbSNP153 33..33 33 - - - 68293 RMVar_ID_68293 Human_SNP_ID_452410229 m1A Human chr10 + 132415362 132415360 132415362 CCACACACATATCCACTCACACACATCCACTCACTGTCACACACGTCACTCACACTCATTTACTC CCACACACATATCCACTCACACACATCCACT__CTGTCACACACGTCACTCACACTCATTTACTC TCA T PWWP2B Ensembl:ENSG00000171813 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132415356..132415442 26863196 MeRIP-seq:(Medium) rs921942197 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2199683 68294 RMVar_ID_68294 Human_SNP_ID_452411666 m1A Human chr10 + 132419403 132419386 132419403 GGTCAGGGGGACACCTGGGAGCGGAACACCTGAGGGAGGAGCACCTGGCGGGGAGCCTTGGGGGA GGTCAGGGGGACACCT_________________GGGAGGAGCACCTGGCGGGGAGCCTTGGGGGA TGGGAGCGGAACACCTGA T AL451069.2 Ensembl:ENSG00000231705 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132419354..132419444 26863196 MeRIP-seq:(Medium) rs777111901 Functional Loss DEL dbSNP153 17..33 33 - - - 68295 RMVar_ID_68295 Human_SNP_ID_452414488 m1A Human chr10 + 132427926 132427924 132427927 CCACCATCACTCTCACTGTCATCACAATCACCATCATCATCATCACCATCACTATCACTGTCACC CCACCATCACTCTCACTGTCATCACAATCAC___CATCATCATCACCATCACTATCACTGTCACC CCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132427875..132427975 26863196 MeRIP-seq:(Medium) rs912771621 Functional Loss DEL dbSNP153 32..34 33 - - - 68296 RMVar_ID_68296 Human_SNP_ID_452414489 m1A Human chr10 + 132427926 132427926 132427926 CCACCATCACTCTCACTGTCATCACAATCACCATCATCATCATCACCATCACTATCACTGTCACC CCACCATCACTCTCACTGTCATCACAATCACCGTCATCATCATCACCATCACTATCACTGTCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132427875..132427975 26863196 MeRIP-seq:(Medium) rs374823447 Functional Loss SNV dbSNP153 33..33 33 - - - 68297 RMVar_ID_68297 Human_SNP_ID_452419889 m1A Human chr10 + 132445222 132445222 132445222 CAGGATCTGCCAGGACTGGGAAGGGAGGCAGGAGGCTTCTCTGGGTATAAAGCAGCTGAAATGTG CAGGATCTGCCAGGACTGGGAAGGGAGGCAGGGGGCTTCTCTGGGTATAAAGCAGCTGAAATGTG A G LINC02870 Ensembl:ENSG00000180066 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:132445174..132445760;chr10:132445171..132445318 26863196 MeRIP-seq:(Medium) rs775686870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1190263,Human_Splice_Rec_1190267 68298 RMVar_ID_68298 Human_SNP_ID_452421042 m1A Human chr10 - 132448781 132448781 132448781 GAGGGGCCGGGCAGGACTGGGGCAAGGGTGGGAGGGGCCGGGCCGGACTGGGGCAAGGGTGGGAG GAGGGGCCGGGCAGGACTGGGGCAAGGGTGGGCGGGGCCGGGCCGGACTGGGGCAAGGGTGGGAG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:132448684..132448840 26863410 MeRIP-seq:(Medium) rs1426046066 Functional Loss SNV dbSNP153 33..33 33 - - - 68299 RMVar_ID_68299 Human_SNP_ID_452446220 m1A Human chr10 + 132537952 132537952 132537952 CGCGAGGCCGGAGCCCCGGCCAGGCCCGGCCGACCCGCCGAGCCCGCGATGCGCCCCGGGGCCGC CGCGAGGCCGGAGCCCCGGCCAGGCCCGGCCGCCCCGCCGAGCCCGCGATGCGCCCCGGGGCCGC A C INPP5A Ensembl:ENSG00000068383 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:132537851..132538166 26863410 MeRIP-seq:(Medium) rs1005446045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68300 RMVar_ID_68300 Human_SNP_ID_452450243 m1A Human chr10 - 132552747 132552739 132552747 TATTCCCCCAAGGCTCTGAGAAGGCGTTCACCAATCCTCCCTCCCTATCCTACCCAATATGCCAC TATTCCCCCAAGGCTCTGAGAAGGCGTTCACC________CTCCCTATCCTACCCAATATGCCAC GGGAGGATT G lnc-STK32C-7,lnc-STK32C-7:2,lnc-STK32C-7:3 RNACentral:URS00008B7975,RNACentral:URS00008BFB70,RNACentral:URS00008BEC79 lincRNA,lincRNA,lincRNA intron,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132552738..132552860 26863196 MeRIP-seq:(Medium) rs1358390873 Functional Loss DEL dbSNP153 33..40 33 - - - 68301 RMVar_ID_68301 Human_SNP_ID_452450402 m1A Human chr10 + 132553381 132553381 132553381 ATATTGAGTGGGATAGGGAGGGAGGACTGGTGAACGCCTTCTCAGAGCCTTGGTGGAATATTGAG ATATTGAGTGGGATAGGGAGGGAGGACTGGTGGACGCCTTCTCAGAGCCTTGGTGGAATATTGAG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:132553345..132553504 26863196 MeRIP-seq:(Medium) rs1564913551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68302 RMVar_ID_68302 Human_SNP_ID_452450927 m1A Human chr10 + 132555089 132555089 132555089 GCGTGGTTGGCATTGATGTGGGTAGCATGGGCAGTGTGGGTGGCATGGCTGCTGTGGGTGACATA GCGTGGTTGGCATTGATGTGGGTAGCATGGGCCGTGTGGGTGGCATGGCTGCTGTGGGTGACATA A C INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132554380..132555244 26863196 MeRIP-seq:(Medium) rs1282054843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364288,Human_RBP_ID_5313394,Human_RBP_ID_8172467,Human_RBP_ID_21964194 RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68303 RMVar_ID_68303 Human_SNP_ID_452451060 m1A Human chr10 + 132555471 132555471 132555471 GGCTTGGGCTGGGGCGTGGCCACGCTGGGAGGATGAGGAGCTTGAAGTGACTCAGGGGACCTGGC GGCTTGGGCTGGGGCGTGGCCACGCTGGGAGGTTGAGGAGCTTGAAGTGACTCAGGGGACCTGGC A T INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132555468..132555567 26863196 MeRIP-seq:(Medium) rs1319995998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3363643,Human_RBP_ID_5163427,Human_RBP_ID_5234694,Human_RBP_ID_5643161,Human_RBP_ID_8059066,Human_RBP_ID_8172468,Human_RBP_ID_8940433,Human_RBP_ID_9413435,Human_RBP_ID_18476560,Human_RBP_ID_21915812,Human_RBP_ID_21964638 RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68304 RMVar_ID_68304 Human_SNP_ID_452456082 m1A Human chr10 - 132573515 132573515 132573515 CAACCCAACATCAACAAAACCTCACACAGCACACACACCCCAACATCTCAACAAAACCTCACACG CAACCCAACATCAACAAAACCTCACACAGCACGCACACCCCAACATCTCAACAAAACCTCACACG T C lnc-NKX6-2-6,lnc-NKX6-2-6:2 RNACentral:URS0000E9CD67,RNACentral:URS00008B76E2 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132573496..132573599 26863196 MeRIP-seq:(Medium) rs1183832047 Functional Loss SNV dbSNP153 33..33 33 - - - 68305 RMVar_ID_68305 Human_SNP_ID_452456233 m1A Human chr10 + 132573987 132573951 132573988 CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTACGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG __________________________________GTGCCGTGGGAGGTTTTGTTGAGATGTTGGG TGTGCCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTAC T INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132573968..132574037 26863196 MeRIP-seq:(Medium) rs1564921031 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68306 RMVar_ID_68306 Human_SNP_ID_452456237 m1A Human chr10 - 132573960 132573960 132573960 GCACGTACACCCCAACATCTCAACAAAACCTCACACGGCACACACACCTCAACATCAACAAAACC GCACGTACACCCCAACATCTCAACAAAACCTCCCACGGCACACACACCTCAACATCAACAAAACC T G lnc-NKX6-2-6,lnc-NKX6-2-6:2 RNACentral:URS0000E9CD67,RNACentral:URS00008B76E2 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132573958..132574041 26863196 MeRIP-seq:(Medium) rs60418419 Functional Loss SNV dbSNP153 33..33 33 - - - 68307 RMVar_ID_68307 Human_SNP_ID_452456243 m1A Human chr10 + 132573987 132573985 132573987 CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTACGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG CCGTGTGAGGTTTTGTTGAGATGTTGGGGTG__CGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG GTA G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132573968..132574037 26863196 MeRIP-seq:(Medium) rs202028956 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68308 RMVar_ID_68308 Human_SNP_ID_452456246 m1A Human chr10 + 132573987 132573987 132573987 CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTACGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTGCGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132573968..132574037 26863196 MeRIP-seq:(Medium) rs2814441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 68309 RMVar_ID_68309 Human_SNP_ID_452457673 m1A Human chr10 - 132579139 132579139 132579139 GCCCGCAACCGGCGCGGCTCTGCCTCCCTGCCACTCAGAAGCCCAGCTCATTTCACAGCTGCCCG GCCCGCAACCGGCGCGGCTCTGCCTCCCTGCCTCTCAGAAGCCCAGCTCATTTCACAGCTGCCCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132579129..132579539 26863196 MeRIP-seq:(Medium) rs1268230021 Functional Loss SNV dbSNP153 33..33 33 - - - 68310 RMVar_ID_68310 Human_SNP_ID_452466692 m1A Human chr10 + 132611684 132611684 132611684 GGGCAGGGGAGAGGCCCTGTCAGGGGAGGGTGAGGGAGGTGAGGTGGGCAGGGGAGAGGCCCTGT GGGCAGGGGAGAGGCCCTGTCAGGGGAGGGTGGGGGAGGTGAGGTGGGCAGGGGAGAGGCCCTGT A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132611682..132611811 26863196 MeRIP-seq:(Medium) rs1373411908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83302,RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_324260,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265,RMVar_hsa_circ_374607,RMVar_hsa_circ_374808,RMVar_hsa_circ_358766,RMVar_hsa_circ_306188,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_147271,RMVar_hsa_circ_147273,RMVar_hsa_circ_81340,RMVar_hsa_circ_147272,RMVar_hsa_circ_147270,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266 68311 RMVar_ID_68311 Human_SNP_ID_452466693 m1A Human chr10 + 132611684 132611684 132611684 GGGCAGGGGAGAGGCCCTGTCAGGGGAGGGTGAGGGAGGTGAGGTGGGCAGGGGAGAGGCCCTGT GGGCAGGGGAGAGGCCCTGTCAGGGGAGGGTGTGGGAGGTGAGGTGGGCAGGGGAGAGGCCCTGT A T INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132611682..132611811 26863196 MeRIP-seq:(Medium) rs1373411908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83302,RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_324260,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265,RMVar_hsa_circ_374607,RMVar_hsa_circ_374808,RMVar_hsa_circ_358766,RMVar_hsa_circ_306188,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_147271,RMVar_hsa_circ_147273,RMVar_hsa_circ_81340,RMVar_hsa_circ_147272,RMVar_hsa_circ_147270,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266 68312 RMVar_ID_68312 Human_SNP_ID_452466705 m1A Human chr10 + 132611719 132611719 132611719 GAGGTGAGGTGGGCAGGGGAGAGGCCCTGTCCAGGGAGGGTGAGGGAGGTGAGGAGTTCATGGGA GAGGTGAGGTGGGCAGGGGAGAGGCCCTGTCCGGGGAGGGTGAGGGAGGTGAGGAGTTCATGGGA A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:132611702..132611864 26863196 MeRIP-seq:(Medium) rs926721411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172487 RMVar_hsa_circ_83302,RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_324260,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265,RMVar_hsa_circ_374607,RMVar_hsa_circ_374808,RMVar_hsa_circ_358766,RMVar_hsa_circ_306188,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_147271,RMVar_hsa_circ_147273,RMVar_hsa_circ_81340,RMVar_hsa_circ_147272,RMVar_hsa_circ_147270,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266 68313 RMVar_ID_68313 Human_SNP_ID_452466790 m1A Human chr10 - 132611876 132611876 132611876 CACCCTCCTCTGATGGGGCCTCTCCCCTGCCCACTTCACCTCCCACACCCTCCTCTGACGGGGCC CACCCTCCTCTGATGGGGCCTCTCCCCTGCCCTCTTCACCTCCCACACCCTCCTCTGACGGGGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132611864..132612326 26863196 MeRIP-seq:(Medium) rs1157984184 Functional Loss SNV dbSNP153 33..33 33 - - - 68314 RMVar_ID_68314 Human_SNP_ID_452466791 m1A Human chr10 - 132611876 132611876 132611876 CACCCTCCTCTGATGGGGCCTCTCCCCTGCCCACTTCACCTCCCACACCCTCCTCTGACGGGGCC CACCCTCCTCTGATGGGGCCTCTCCCCTGCCCCCTTCACCTCCCACACCCTCCTCTGACGGGGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132611864..132612326 26863196 MeRIP-seq:(Medium) rs1157984184 Functional Loss SNV dbSNP153 33..33 33 - - - 68315 RMVar_ID_68315 Human_SNP_ID_452472831 m1A Human chr10 + 132634359 132634359 132634359 TCTCCCTTGGTGGGTGTGCCCCGGAGAGGCGTATCATCTCCCTTGGTGGGTGTGCCCCAGAGAGG TCTCCCTTGGTGGGTGTGCCCCGGAGAGGCGTGTCATCTCCCTTGGTGGGTGTGCCCCAGAGAGG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132634347..132634547 26863196 MeRIP-seq:(Medium) rs376995973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83302,RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_324260,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265,RMVar_hsa_circ_374607,RMVar_hsa_circ_374808,RMVar_hsa_circ_358766,RMVar_hsa_circ_306188,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_147271,RMVar_hsa_circ_147273,RMVar_hsa_circ_81340,RMVar_hsa_circ_147272,RMVar_hsa_circ_147270,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266 68316 RMVar_ID_68316 Human_SNP_ID_452488836 m1A Human chr10 + 132691908 132691908 132691908 ACGTGTGGTCGCGGGAGACATGCGGTCGCGGGAGACGTGTGGTCGCGGGGTGTGCGGTCGCGGGA ACGTGTGGTCGCGGGAGACATGCGGTCGCGGGCGACGTGTGGTCGCGGGGTGTGCGGTCGCGGGA A C INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132691723..132692017 26863196 MeRIP-seq:(Medium) rs927042921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324260,RMVar_hsa_circ_374808,RMVar_hsa_circ_358766,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_2468,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_81340,RMVar_hsa_circ_147270,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266,RMVar_hsa_circ_352649,RMVar_hsa_circ_319880,RMVar_hsa_circ_319259,RMVar_hsa_circ_72285,RMVar_hsa_circ_82733,RMVar_hsa_circ_147275,RMVar_hsa_circ_147276,RMVar_hsa_circ_271992,RMVar_hsa_circ_313476,RMVar_hsa_circ_346323,RMVar_hsa_circ_276842,RMVar_hsa_circ_88981,RMVar_hsa_circ_147278,RMVar_hsa_circ_147279,RMVar_hsa_circ_147280,RMVar_hsa_circ_147277 68317 RMVar_ID_68317 Human_SNP_ID_452491911 m1A Human chr10 + 132703682 132703682 132703682 GCACACCCCCACACACACACACGTGCAGCTTCACCCCCGCAGACACATGCGGCTTCACCCCCCCC GCACACCCCCACACACACACACGTGCAGCTTCCCCCCCGCAGACACATGCGGCTTCACCCCCCCC A C INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:132703599..132703686 26863410 MeRIP-seq:(Medium) rs1270528128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324260,RMVar_hsa_circ_374808,RMVar_hsa_circ_323834,RMVar_hsa_circ_97534,RMVar_hsa_circ_2468,RMVar_hsa_circ_147267,RMVar_hsa_circ_147269,RMVar_hsa_circ_81340,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266,RMVar_hsa_circ_319880,RMVar_hsa_circ_319259,RMVar_hsa_circ_82733,RMVar_hsa_circ_147275,RMVar_hsa_circ_147276,RMVar_hsa_circ_271992,RMVar_hsa_circ_313476,RMVar_hsa_circ_346323,RMVar_hsa_circ_88981,RMVar_hsa_circ_147278,RMVar_hsa_circ_147279,RMVar_hsa_circ_147280,RMVar_hsa_circ_147277 68318 RMVar_ID_68318 Human_SNP_ID_452495048 m1A Human chr10 + 132713098 132713098 132713098 AGAGCATATGCACGTGGGTTGGATATGTGTGCAGGTACATGTGGGTATGTGTGCATGCAGGTTGT AGAGCATATGCACGTGGGTTGGATATGTGTGCCGGTACATGTGGGTATGTGTGCATGCAGGTTGT A C INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:132713003..132713192 26863196 MeRIP-seq:(Medium) rs567787908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5643180,Human_RBP_ID_8330054 RMVar_hsa_circ_324260,RMVar_hsa_circ_374808,RMVar_hsa_circ_97534,RMVar_hsa_circ_2468,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147268,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147276,RMVar_hsa_circ_313476,RMVar_hsa_circ_346323,RMVar_hsa_circ_147279,RMVar_hsa_circ_147280,RMVar_hsa_circ_350834,RMVar_hsa_circ_85653,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147283,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285 68319 RMVar_ID_68319 Human_SNP_ID_452508049 m1A Human chr10 - 132752617 132752617 132752617 GTCCCTCCATGCCACACCCCACTCCATGCCACACCCCACTCCATGCCACACCCCTCCATGCCACA GTCCCTCCATGCCACACCCCACTCCATGCCACCCCCCACTCCATGCCACACCCCTCCATGCCACA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:132752569..132752728 26863196 MeRIP-seq:(Medium) rs1182478080 Functional Loss SNV dbSNP153 33..33 33 - - - 68320 RMVar_ID_68320 Human_SNP_ID_452508986 m1A Human chr10 - 132755337 132755337 132755337 TCATATGCATGTCTGCTCACACACACGCTCACACAGCTCACACACTCGCCCACTCAAATGCATAT TCATATGCATGTCTGCTCACACACACGCTCACGCAGCTCACACACTCGCCCACTCAAATGCATAT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:132755295..132755457 26863196 MeRIP-seq:(Medium) rs1306539207 Functional Loss SNV dbSNP153 33..33 33 - - - 68321 RMVar_ID_68321 Human_SNP_ID_452509062 m1A Human chr10 + 132755484 132755484 132755484 GTGTGAGCGAGTGTGTGTGAGCAGGCATACGCATATGAGTGGGTGTGTGCATGAGAGCAGGTGTG GTGTGAGCGAGTGTGTGTGAGCAGGCATACGCCTATGAGTGGGTGTGTGCATGAGAGCAGGTGTG A C INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132755398..132755583 26863196 MeRIP-seq:(Medium) rs1480313297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5643189 RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_48674,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68322 RMVar_ID_68322 Human_SNP_ID_452509063 m1A Human chr10 + 132755484 132755484 132755484 GTGTGAGCGAGTGTGTGTGAGCAGGCATACGCATATGAGTGGGTGTGTGCATGAGAGCAGGTGTG GTGTGAGCGAGTGTGTGTGAGCAGGCATACGCTTATGAGTGGGTGTGTGCATGAGAGCAGGTGTG A T INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132755398..132755583 26863196 MeRIP-seq:(Medium) rs1480313297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5643189 RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_48674,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68323 RMVar_ID_68323 Human_SNP_ID_452511179 m1A Human chr10 + 132761577 132761577 132761577 TGCTGAGGATGGCATGGCTGGTGGGGGACAGCACGGTGGGGCGGAGCCTGGGGGTGCCATGCGGA TGCTGAGGATGGCATGGCTGGTGGGGGACAGCGCGGTGGGGCGGAGCCTGGGGGTGCCATGCGGA A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132761425..132761615 26863196 MeRIP-seq:(Medium) rs983212920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_48674,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68324 RMVar_ID_68324 Human_SNP_ID_452515635 m1A Human chr10 + 132774889 132774803 132774890 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG __________________________________GAGGGGCAGGGAGGAGAGAGGGGCACGGAGG AGAGGGGCAGGGAGGAGAGAGGGGCACGGAGGAGAGAGGGGTAGGGAGAGACGGGCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAG A INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs1565013329 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68325 RMVar_ID_68325 Human_SNP_ID_452515682 m1A Human chr10 + 132774889 132774851 132774890 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG __________________________________GAGGGGCAGGGAGGAGAGAGGGGCACGGAGG AGACGGGCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAG A INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs1304418783 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68326 RMVar_ID_68326 Human_SNP_ID_452515695 m1A Human chr10 + 132774889 132774864 132774889 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GCAGGGAG_________________________GGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GGAGGGGCAGGGAGGAGAGGCAGGGA G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs1565013474 Functional Loss DEL dbSNP153 9..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68327 RMVar_ID_68327 Human_SNP_ID_452515706 m1A Human chr10 + 132774889 132774880 132774889 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GCAGGGAGGAGGGGCAGGGAGGAG_________GGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GAGGCAGGGA G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs1263502288 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68328 RMVar_ID_68328 Human_SNP_ID_452515712 m1A Human chr10 + 132774889 132774881 132774890 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GCAGGGAGGAGGGGCAGGGAGGAGA_________GAGGGGCAGGGAGGAGAGAGGGGCACGGAGG AGGCAGGGAG A INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs71013561 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68329 RMVar_ID_68329 Human_SNP_ID_452515721 m1A Human chr10 + 132774889 132774889 132774889 GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGAGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG GCAGGGAGGAGGGGCAGGGAGGAGAGGCAGGGGGGAGGGGCAGGGAGGAGAGAGGGGCACGGAGG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:132774827..132774999 26863196 MeRIP-seq:(Medium) rs1320639318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68330 RMVar_ID_68330 Human_SNP_ID_452515809 m1A Human chr10 + 132775010 132775007 132775010 GGAGGAGGGGCAGGGAGGAGAGAGGGGCAGAGAGGAGGGGCAGGGAGGAGGGGCAGGGAGGAGGG GGAGGAGGGGCAGGGAGGAGAGAGGGGCAG___GGAGGGGCAGGGAGGAGGGGCAGGGAGGAGGG GAGA G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:132774984..132775181 26863196 MeRIP-seq:(Medium) rs1565013708 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68331 RMVar_ID_68331 Human_SNP_ID_452515814 m1A Human chr10 + 132775010 132775010 132775010 GGAGGAGGGGCAGGGAGGAGAGAGGGGCAGAGAGGAGGGGCAGGGAGGAGGGGCAGGGAGGAGGG GGAGGAGGGGCAGGGAGGAGAGAGGGGCAGAGGGGAGGGGCAGGGAGGAGGGGCAGGGAGGAGGG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:132774984..132775181 26863196 MeRIP-seq:(Medium) rs1401446926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97534,RMVar_hsa_circ_147267,RMVar_hsa_circ_81340,RMVar_hsa_circ_147266,RMVar_hsa_circ_116619,RMVar_hsa_circ_82733,RMVar_hsa_circ_147280,RMVar_hsa_circ_102337,RMVar_hsa_circ_147281,RMVar_hsa_circ_147282,RMVar_hsa_circ_113455,RMVar_hsa_circ_147285,RMVar_hsa_circ_67927,RMVar_hsa_circ_122829,RMVar_hsa_circ_147288 68332 RMVar_ID_68332 Human_SNP_ID_452591818 m1A Human chr10 - 133011337 133011337 133011337 ACAAAAACACATCACACAAGCACACATCACACACGCTAACACATCACACAAACACACATCACACA ACAAAAACACATCACACAAGCACACATCACACGCGCTAACACATCACACAAACACACATCACACA T C lnc-CFAP46-3,lnc-CFAP46-3:2,lnc-CFAP46-3:3,lnc-CFAP46-3:4,lnc-CFAP46-3:5,lnc-CFAP46-3:6,lnc-CFAP46-3:7,lnc-CFAP46-3:8,lnc-CFAP46-3:9,lnc-CFAP46-3:10 RNACentral:URS00008BF67D,RNACentral:URS00008C003E,RNACentral:URS00008B69AB,RNACentral:URS00008B4CA3,RNACentral:URS00008BF37C,RNACentral:URS00008B5767,RNACentral:URS00008B40CD,RNACentral:URS00008BA563,RNACentral:URS00008BA327,RNACentral:URS00008B5B8D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,exon,exon,intron,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133011025..133011390 26863196 MeRIP-seq:(Medium) rs149249729 Functional Loss SNV dbSNP153 33..33 33 - - - 68333 RMVar_ID_68333 Human_SNP_ID_452591907 m1A Human chr10 - 133011533 133011530 133011534 CACACACGCTAACACACATCACACACTAACACACATCACACACTAACACACATCACACGTGCTAA CACACACGCTAACACACATCACACACTAACA____TCACACACTAACACACATCACACGTGCTAA ATGTG A lnc-CFAP46-3,lnc-CFAP46-3:2,lnc-CFAP46-3:3,lnc-CFAP46-3:4,lnc-CFAP46-3:5,lnc-CFAP46-3:6,lnc-CFAP46-3:7,lnc-CFAP46-3:8,lnc-CFAP46-3:9,lnc-CFAP46-3:10,lnc-CFAP46-3:11 RNACentral:URS00008BF67D,RNACentral:URS00008C003E,RNACentral:URS00008B69AB,RNACentral:URS00008B4CA3,RNACentral:URS00008BF37C,RNACentral:URS00008B5767,RNACentral:URS00008B40CD,RNACentral:URS00008BA563,RNACentral:URS00008BA327,RNACentral:URS00008BD1D9,RNACentral:URS00008B5B8D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,exon,intron,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133011484..133011579 26863196 MeRIP-seq:(Medium) rs796572554 Functional Loss DEL dbSNP153 32..35 33 - - - 68334 RMVar_ID_68334 Human_SNP_ID_452591908 m1A Human chr10 - 133011533 133011530 133011534 CACACACGCTAACACACATCACACACTAACACACATCACACACTAACACACATCACACGTGCTAA CACACACGCTAACACACATCACACACTAACA__CATCACACACTAACACACATCACACGTGCTAA ATGTG ATG lnc-CFAP46-3,lnc-CFAP46-3:2,lnc-CFAP46-3:3,lnc-CFAP46-3:4,lnc-CFAP46-3:5,lnc-CFAP46-3:6,lnc-CFAP46-3:7,lnc-CFAP46-3:8,lnc-CFAP46-3:9,lnc-CFAP46-3:10,lnc-CFAP46-3:11 RNACentral:URS00008BF67D,RNACentral:URS00008C003E,RNACentral:URS00008B69AB,RNACentral:URS00008B4CA3,RNACentral:URS00008BF37C,RNACentral:URS00008B5767,RNACentral:URS00008B40CD,RNACentral:URS00008BA563,RNACentral:URS00008BA327,RNACentral:URS00008BD1D9,RNACentral:URS00008B5B8D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,exon,intron,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133011484..133011579 26863196 MeRIP-seq:(Medium) rs796572554 Functional Loss DEL dbSNP153 32..33 33 - - - 68335 RMVar_ID_68335 Human_SNP_ID_452617047 m1A Human chr10 + 133086388 133086388 133086388 TCCGTGTGCAGGGAAAGAGACAAGCCAGGGCCACTCCCCCCACCGGCCGGGGCCTCCTCTGGGCC TCCGTGTGCAGGGAAAGAGACAAGCCAGGGCCTCTCCCCCCACCGGCCGGGGCCTCCTCTGGGCC A T ADGRA1 Ensembl:ENSG00000197177 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:133086376..133086425 26863196 MeRIP-seq:(Medium) rs1326257924 Functional Loss SNV dbSNP153 33..33 33 - - - 68336 RMVar_ID_68336 Human_SNP_ID_452665693 m1A Human chr10 - 133231026 133231026 133231026 GGCGTCCGCAGACTTCGGTGGGGACGGGCTGAAGCGGAGCGTCCAGGTGGGGTCCGCGTCGCGGT GGCGTCCGCAGACTTCGGTGGGGACGGGCTGAGGCGGAGCGTCCAGGTGGGGTCCGCGTCGCGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:133230803..133231269 26863410 MeRIP-seq:(Medium) rs1490100886 Functional Loss SNV dbSNP153 33..33 33 - - - 68337 RMVar_ID_68337 Human_SNP_ID_452677393 m1A Human chr10 - 133264788 133264788 133264788 AGGTAGGTGGGGCAGAGGCTGCAGCAGGAACCAGGCATGGAGGTAGATGCGGCAGAGGCTGCAGC AGGTAGGTGGGGCAGAGGCTGCAGCAGGAACCGGGCATGGAGGTAGATGCGGCAGAGGCTGCAGC T C ADAM8 Ensembl:ENSG00000151651 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133264707..133264852 26863196 MeRIP-seq:(Medium) rs1369079531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5948139,Human_RBP_ID_23304228 68338 RMVar_ID_68338 Human_SNP_ID_452677394 m1A Human chr10 - 133264788 133264788 133264788 AGGTAGGTGGGGCAGAGGCTGCAGCAGGAACCAGGCATGGAGGTAGATGCGGCAGAGGCTGCAGC AGGTAGGTGGGGCAGAGGCTGCAGCAGGAACCCGGCATGGAGGTAGATGCGGCAGAGGCTGCAGC T G ADAM8 Ensembl:ENSG00000151651 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133264707..133264852 26863196 MeRIP-seq:(Medium) rs1369079531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5948139,Human_RBP_ID_23304228 68339 RMVar_ID_68339 Human_SNP_ID_452677455 m1A Human chr10 + 133264948 133264948 133264948 CTGCAGCCTCTGCCCCATCTACCTCCACGCGCAGCTCCTGCTGCAGCCTCTGCCCCATCTACCTC CTGCAGCCTCTGCCCCATCTACCTCCACGCGCGGCTCCTGCTGCAGCCTCTGCCCCATCTACCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:133264924..133265073;chr10:133264914..133265057 26863196 MeRIP-seq:(Medium) rs1258218570 Functional Loss SNV dbSNP153 33..33 33 - - - 68340 RMVar_ID_68340 Human_SNP_ID_452683244 m1A Human chr10 + 133280883 133280883 133280883 GGGGGAAGGCTGAGCCGGGGCAGCACTGGGCCAGGGCGGTGCTGGGCAGGGGCAGGCGCTGGGCT GGGGGAAGGCTGAGCCGGGGCAGCACTGGGCCGGGGCGGTGCTGGGCAGGGGCAGGCGCTGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133280872..133280953 26863196 MeRIP-seq:(Medium) rs1323519686 Functional Loss SNV dbSNP153 33..33 33 - - - 68341 RMVar_ID_68341 Human_SNP_ID_452685008 m1A Human chr10 + 133285552 133285552 133285552 TCAGCGCCAGCTCCGTGGGGTCGGCGTGCGCCATCGCCTTCTCCTGCTTGGTCTCGATGGCCAGG TCAGCGCCAGCTCCGTGGGGTCGGCGTGCGCCGTCGCCTTCTCCTGCTTGGTCTCGATGGCCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133285501..133285666 26863196 MeRIP-seq:(Medium) rs1292787527 Functional Loss SNV dbSNP153 33..33 33 - - - 68342 RMVar_ID_68342 Human_SNP_ID_452688274 m1A Human chr10 + 133293110 133293110 133293110 GGATGTAGAACCAGAGCTTCTGCAGCGAAAGGAGGCCCTGCCTGTGCAGCTGCTCCAGCTGTGAC GGATGTAGAACCAGAGCTTCTGCAGCGAAAGGGGGCCCTGCCTGTGCAGCTGCTCCAGCTGTGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:133293064..133293165 32194978 MeRIP-seq:(Medium) rs763052834 Functional Loss SNV dbSNP153 33..33 33 - - - 68343 RMVar_ID_68343 Human_SNP_ID_452690451 m1A Human chr10 - 133300057 133300057 133300057 ACTCCAGAAGACTTTCTAAAGAAATATGATGAACTGAAATCTAAAAATACAAGGAACCTTGACCC ACTCCAGAAGACTTTCTAAAGAAATATGATGAGCTGAAATCTAAAAATACAAGGAACCTTGACCC T C TUBGCP2 Ensembl:ENSG00000130640 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:133299600..133300181 32194978 MeRIP-seq:(Medium) rs1390975108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1763363,Human_RBP_ID_4113686,Human_RBP_ID_18590730,Human_RBP_ID_24795072 Human_Splice_Rec_1190978,Human_Splice_Rec_1190979,Human_Splice_Rec_1191010,Human_Splice_Rec_1191011,Human_Splice_Rec_1191044,Human_Splice_Rec_1191045,Human_Splice_Rec_1191080,Human_Splice_Rec_1191081,Human_Splice_Rec_1191134,Human_Splice_Rec_1191135,Human_Splice_Rec_1191169,Human_Splice_Rec_1191176,Human_Splice_Rec_1191177 RMVar_hsa_circ_6933,RMVar_hsa_circ_119302,RMVar_hsa_circ_41802,RMVar_hsa_circ_147301,RMVar_hsa_circ_329236,RMVar_hsa_circ_103482,RMVar_hsa_circ_20933,RMVar_hsa_circ_347940,RMVar_hsa_circ_67277,RMVar_hsa_circ_124783,RMVar_hsa_circ_147304,RMVar_hsa_circ_147305,RMVar_hsa_circ_302694,RMVar_hsa_circ_147306 68344 RMVar_ID_68344 Human_SNP_ID_452693260 m1A Human chr10 + 133308944 133308944 133308944 CCGACAGGCTGCGCCCGCCCGCGCCCGGGGTGATGCAGTTGCCCCCCGCGCTGTGCGCCCGCCTC CCGACAGGCTGCGCCCGCCCGCGCCCGGGGTGTTGCAGTTGCCCCCCGCGCTGTGCGCCCGCCTC A T ZNF511 Ensembl:ENSG00000198546 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:133308933..133309116 26863196 MeRIP-seq:(Medium) rs1179731347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136113 RMVar_hsa_circ_124800,RMVar_hsa_circ_147309 68345 RMVar_ID_68345 Human_SNP_ID_452693282 m1A Human chr10 - 133308965 133308965 133308965 CGCCGCCCCGGGCCCCGCAGCGAGGCGGGCGCACAGCGCGGGGGGCAACTGCATCACCCCGGGCG CGCCGCCCCGGGCCCCGCAGCGAGGCGGGCGCGCAGCGCGGGGGGCAACTGCATCACCCCGGGCG T C TUBGCP2 Ensembl:ENSG00000130640 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133308923..133309094 26863196 MeRIP-seq:(Medium) rs1564777082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137165 RMVar_hsa_circ_91092,RMVar_hsa_circ_147308 68346 RMVar_ID_68346 Human_SNP_ID_452693306 m1A Human chr10 - 133309005 133309005 133309005 CGGCCCCAGCCGCGGGATCCCGCTCTACAGGCAGCGGCTCCGCCGCCCCGGGCCCCGCAGCGAGG CGGCCCCAGCCGCGGGATCCCGCTCTACAGGCCGCGGCTCCGCCGCCCCGGGCCCCGCAGCGAGG T G TUBGCP2 Ensembl:ENSG00000130640 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:133308956..133309156 26863196 MeRIP-seq:(Medium) rs1229501899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137165 RMVar_hsa_circ_91092,RMVar_hsa_circ_147308 68347 RMVar_ID_68347 Human_SNP_ID_452693337 m1A Human chr10 + 133309080 133309080 133309080 CTTCGTTGCGCGCCCCGTGCGCTTCCCGCGGGAGCACCAGTTCTTCGAGGTGCGTGAGCAAAAGA CTTCGTTGCGCGCCCCGTGCGCTTCCCGCGGGCGCACCAGTTCTTCGAGGTGCGTGAGCAAAAGA A C ZNF511 Ensembl:ENSG00000198546 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr10:133308970..133309124;chr10:133308970..133309824 32194978 MeRIP-seq:(Medium) rs774180033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136584 Human_Splice_Rec_1191185,Human_Splice_Rec_1191195,Human_Splice_Rec_1191203 RMVar_hsa_circ_124800,RMVar_hsa_circ_147309 68348 RMVar_ID_68348 Human_SNP_ID_452694411 m1A Human chr10 - 133311843 133311836 133311843 GAGAACGGGTTTCAGAAAGAGCTCAGACACTGACCTATGTCTGTAGATCCGCCTCTCACCTGCCG GAGAACGGGTTTCAGAAAGAGCTCAGACACTG_______TCTGTAGATCCGCCTCTCACCTGCCG ACATAGGT A TUBGCP2 Ensembl:ENSG00000130640 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:133311773..133311887 32194978 MeRIP-seq:(Medium) rs758402951 Functional Loss DEL dbSNP153 33..39 33 - - - 68349 RMVar_ID_68349 Human_SNP_ID_452694878 m1A Human chr10 - 133313008 133313008 133313008 GGGTCCCTCACAGCTTCTGATGACAGCTGCTAATGCCATTTGCTGAGGAACAAGGATGGGGAGGA GGGTCCCTCACAGCTTCTGATGACAGCTGCTACTGCCATTTGCTGAGGAACAAGGATGGGGAGGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:133312764..133313075 32194978 MeRIP-seq:(Medium) rs995913738 Functional Loss SNV dbSNP153 33..33 33 - - - 68350 RMVar_ID_68350 Human_SNP_ID_452699001 m1A Human chr10 + 133324772 133324733 133324773 GCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGGAGA __________________________________GCTGGGGCTGGGGTGGGGATGCTGGGGGAGA GGCTGGGGCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGAT G ZNF511-PRAP1 Ensembl:ENSG00000283496 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133324762..133324861 26863196 MeRIP-seq:(Medium) rs762101182 Functional Loss DEL dbSNP153 1..34 33 - - - 68351 RMVar_ID_68351 Human_SNP_ID_452699002 m1A Human chr10 + 133324772 133324733 133324773 GCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGGAGA GCTGGGGTGGGGAT____________________GCTGGGGCTGGGGTGGGGATGCTGGGGGAGA GGCTGGGGCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGAT GGCTGGGGCTGGGGTGGGGAT ZNF511-PRAP1 Ensembl:ENSG00000283496 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133324762..133324861 26863196 MeRIP-seq:(Medium) rs762101182 Functional Loss DEL dbSNP153 15..34 33 - - - 68352 RMVar_ID_68352 Human_SNP_ID_452699014 m1A Human chr10 + 133324772 133324772 133324772 GCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGATGCTGGGGGAGA GCTGGGGTGGGGATGCTGGGGCTGGGGTGGGGGTGCTGGGGCTGGGGTGGGGATGCTGGGGGAGA A G ZNF511-PRAP1 Ensembl:ENSG00000283496 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133324762..133324861 26863196 MeRIP-seq:(Medium) rs1029327371 Functional Loss SNV dbSNP153 33..33 33 - - - 68353 RMVar_ID_68353 Human_SNP_ID_452699062 m1A Human chr10 + 133324964 133324964 133324964 ACGCCCCCATTCACTCCTTTCTTCACTTGGTCATTTATGCCTGTGGGCCACACATCTAGGAGGCA ACGCCCCCATTCACTCCTTTCTTCACTTGGTCCTTTATGCCTGTGGGCCACACATCTAGGAGGCA A C ZNF511-PRAP1 Ensembl:ENSG00000283496 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133324959..133325059 26863196 MeRIP-seq:(Medium) rs900486370 Functional Loss SNV dbSNP153 33..33 33 - - - 68354 RMVar_ID_68354 Human_SNP_ID_452706621 m1A Human chr10 - 133349317 133349313 133349318 GTTCGGGGGTGCGTGTGCTGTGTGTGTATGTTATGTGTGTTTGTGTGTGGTGGATGTGTGTGTAT GTTCGGGGGTGCGTGTGCTGTGTGTGTATGT_____GTGTTTGTGTGTGGTGGATGTGTGTGTAT CACATA C AL360181.1 Ensembl:ENSG00000226699 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133349207..133349497 26863196 MeRIP-seq:(Medium) rs1381209968 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_23445667 68355 RMVar_ID_68355 Human_SNP_ID_452709083 m1A Human chr10 + 133357358 133357356 133357358 CACCCAGTCATGGCGGCAGATCGTGGGTCACAAGAGGTCTCAGGTCAGCCAGTTGGGCGCCCCCA CACCCAGTCATGGCGGCAGATCGTGGGTCAC__GAGGTCTCAGGTCAGCCAGTTGGGCGCCCCCA CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133357342..133357494 26863196 MeRIP-seq:(Medium) rs1458866349 Functional Loss DEL dbSNP153 32..33 33 - - - 68356 RMVar_ID_68356 Human_SNP_ID_452710718 m1A Human chr10 + 133362814 133362814 133362814 AAAAGAGGATGATTTACTTGCTTCTAAAACTGACAGGCTGCACTTGTCCTCTCCAAGCAGAGGTG AAAAGAGGATGATTTACTTGCTTCTAAAACTGGCAGGCTGCACTTGTCCTCTCCAAGCAGAGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133362547..133362887 26863196 MeRIP-seq:(Medium) rs376401874 Functional Loss SNV dbSNP153 33..33 33 - - - 68357 RMVar_ID_68357 Human_SNP_ID_452712986 m1A Human chr10 - 133369953 133369953 133369953 TTACTCCAGCAAGTTCTTGAAGCACTGGGACCACCTCACCCAGGTCAAGAAGCCAGTCATCGCTG TTACTCCAGCAAGTTCTTGAAGCACTGGGACCGCCTCACCCAGGTCAAGAAGCCAGTCATCGCTG T C ECHS1 Ensembl:ENSG00000127884 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:133369901..133370050 32194978 MeRIP-seq:(Medium) rs769170809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374358,Human_RBP_ID_1444334,Human_RBP_ID_8330138 Human_Splice_Rec_1191328,Human_Splice_Rec_1191329 Human_miRNA_ID_2007036 RMVar_hsa_circ_12978,RMVar_hsa_circ_106076,RMVar_hsa_circ_116135,RMVar_hsa_circ_81001,RMVar_hsa_circ_147321,RMVar_hsa_circ_147322,RMVar_hsa_circ_147320,RMVar_hsa_circ_103177,RMVar_hsa_circ_147323 68358 RMVar_ID_68358 Human_SNP_ID_452713270 m1A Human chr10 - 133370752 133370752 133370752 ATACCCCTTTTTGCCTTCTTGCTCCAGGTGCTAACTTTGAGTACATCATCGCAGAAAAAAGAGGG ATACCCCTTTTTGCCTTCTTGCTCCAGGTGCTGACTTTGAGTACATCATCGCAGAAAAAAGAGGG T C ECHS1 Ensembl:ENSG00000127884 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133370726..133370775 26863196 MeRIP-seq:(Medium) rs1204252549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136588 Human_Splice_Rec_1191326 RMVar_hsa_circ_12978,RMVar_hsa_circ_106076,RMVar_hsa_circ_81001,RMVar_hsa_circ_147321,RMVar_hsa_circ_147322,RMVar_hsa_circ_103177,RMVar_hsa_circ_147323 68359 RMVar_ID_68359 Human_SNP_ID_452713272 m1A Human chr10 + 133370756 133370756 133370756 CTTTTTTCTGCGATGATGTACTCAAAGTTAGCACCTGGAGCAAGAAGGCAAAAAGGGGTATCTAT CTTTTTTCTGCGATGATGTACTCAAAGTTAGCGCCTGGAGCAAGAAGGCAAAAAGGGGTATCTAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133370726..133370775 26863196 MeRIP-seq:(Medium) rs774009660 Functional Loss SNV dbSNP153 33..33 33 - - - 68360 RMVar_ID_68360 Human_SNP_ID_452714175 m1A Human chr10 + 133373302 133373302 133373302 GACAGCGAACCGGGGGCCTCAGCGGGCCGCGGACGCAGGACAGCAGGACACGCAGGGCGGCCATG GACAGCGAACCGGGGGCCTCAGCGGGCCGCGGGCGCAGGACAGCAGGACACGCAGGGCGGCCATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133373215..133373686 26863196 MeRIP-seq:(Medium) rs10466126 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 68361 RMVar_ID_68361 Human_SNP_ID_452714180 m1A Human chr10 + 133373306 133373306 133373306 GCGAACCGGGGGCCTCAGCGGGCCGCGGACGCAGGACAGCAGGACACGCAGGGCGGCCATGGCTC GCGAACCGGGGGCCTCAGCGGGCCGCGGACGCGGGACAGCAGGACACGCAGGGCGGCCATGGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:133373194..133373350;chr10:133373191..133373719;chr10:133373192..133373698 26863196 MeRIP-seq:(Medium) rs1051394800 Functional Loss SNV dbSNP153 33..33 33 - - - 68362 RMVar_ID_68362 Human_SNP_ID_452716204 m1A Human chr10 - 133379369 133379369 133379369 CCGCGCCCAGCCCCGCGATGCCGCCGCCCACCACCAGCACCCGGGGTCCGCCCGGGGCCTCCCCG CCGCGCCCAGCCCCGCGATGCCGCCGCCCACCCCCAGCACCCGGGGTCCGCCCGGGGCCTCCCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133379319..133379388 26863196 MeRIP-seq:(Medium) rs1007914833 Functional Loss SNV dbSNP153 33..33 33 - - - 68363 RMVar_ID_68363 Human_SNP_ID_452720716 m1A Human chr10 + 133394210 133394210 133394210 AGAGGAGGTCAGCTGCGGGAGCGTTTCCGGGGACGGTGCCGCCATGAGATTGACCCCGCGCGCGC AGAGGAGGTCAGCTGCGGGAGCGTTTCCGGGGGCGGTGCCGCCATGAGATTGACCCCGCGCGCGC A G AL360181.3,MTG1 Ensembl:ENSG00000254536,Ensembl:ENSG00000148824 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133394140..133394271 26863196 MeRIP-seq:(Medium) rs1321312113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416204,Human_RBP_ID_18468835,Human_RBP_ID_18476566,Human_RBP_ID_18590781,Human_RBP_ID_18970514 68364 RMVar_ID_68364 Human_SNP_ID_452720730 m1A Human chr10 - 133394222 133394222 133394222 CGGCGCTGCACAGCGCGCGCGGGGTCAATCTCATGGCGGCACCGTCCCCGGAAACGCTCCCGCAG CGGCGCTGCACAGCGCGCGCGGGGTCAATCTCCTGGCGGCACCGTCCCCGGAAACGCTCCCGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:133394121..133394350;chr10:133394143..133394350 26863196 MeRIP-seq:(Medium) rs1262274240 Functional Loss SNV dbSNP153 33..33 33 - - - 68365 RMVar_ID_68365 Human_SNP_ID_452720733 m1A Human chr10 + 133394226 133394226 133394226 GGGAGCGTTTCCGGGGACGGTGCCGCCATGAGATTGACCCCGCGCGCGCTGTGCAGCGCCGCCCA GGGAGCGTTTCCGGGGACGGTGCCGCCATGAGCTTGACCCCGCGCGCGCTGTGCAGCGCCGCCCA A C AL360181.3,MTG1 Ensembl:ENSG00000254536,Ensembl:ENSG00000148824 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133394139..133394369 26863196 MeRIP-seq:(Medium) rs777231381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137177,Human_RBP_ID_18416204,Human_RBP_ID_18468835,Human_RBP_ID_18476566,Human_RBP_ID_18590782,Human_RBP_ID_18970514 68366 RMVar_ID_68366 Human_SNP_ID_452720734 m1A Human chr10 + 133394226 133394226 133394226 GGGAGCGTTTCCGGGGACGGTGCCGCCATGAGATTGACCCCGCGCGCGCTGTGCAGCGCCGCCCA GGGAGCGTTTCCGGGGACGGTGCCGCCATGAGGTTGACCCCGCGCGCGCTGTGCAGCGCCGCCCA A G AL360181.3,MTG1 Ensembl:ENSG00000254536,Ensembl:ENSG00000148824 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133394139..133394369 26863196 MeRIP-seq:(Medium) rs777231381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137177,Human_RBP_ID_18416204,Human_RBP_ID_18468835,Human_RBP_ID_18476566,Human_RBP_ID_18590782,Human_RBP_ID_18970514 68367 RMVar_ID_68367 Human_SNP_ID_452720735 m1A Human chr10 - 133394227 133394227 133394227 CTGGGCGGCGCTGCACAGCGCGCGCGGGGTCAATCTCATGGCGGCACCGTCCCCGGAAACGCTCC CTGGGCGGCGCTGCACAGCGCGCGCGGGGTCAGTCTCATGGCGGCACCGTCCCCGGAAACGCTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:133394176..133394613 26863196 MeRIP-seq:(Medium) rs1466822676 Functional Loss SNV dbSNP153 33..33 33 - - - 68368 RMVar_ID_68368 Human_SNP_ID_452720880 m1A Human chr10 - 133394468 133394468 133394468 GCGGCTCCGGGAGCGGGTGAGAGCGGGGAAGGAGGGGAGACAAGGGAGGAGGGGCGGGGCCAGCC GCGGCTCCGGGAGCGGGTGAGAGCGGGGAAGGCGGGGAGACAAGGGAGGAGGGGCGGGGCCAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133394465..133394649 26863196 MeRIP-seq:(Medium) rs1353242261 Functional Loss SNV dbSNP153 33..33 33 - - - 68369 RMVar_ID_68369 Human_SNP_ID_452721340 m1A Human chr10 + 133395667 133395667 133395667 TTCTGGACGGTTCAGCTTGAATCGATCACTCTAGAAAGGTTGTGAGCCCCTTCGCTGAGGCGTCC TTCTGGACGGTTCAGCTTGAATCGATCACTCTGGAAAGGTTGTGAGCCCCTTCGCTGAGGCGTCC A G AL360181.3,MTG1 Ensembl:ENSG00000254536,Ensembl:ENSG00000148824 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:133395665..133395805 26863196 MeRIP-seq:(Medium) rs781142994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22640714 68370 RMVar_ID_68370 Human_SNP_ID_452721414 m1A Human chr10 - 133395779 133395779 133395779 GCAGAGGGGCCTCCCCTGCTCTGTGAAAGGATATCCGGGCATCGTGGACCTCGATGATACAGTCC GCAGAGGGGCCTCCCCTGCTCTGTGAAAGGATTTCCGGGCATCGTGGACCTCGATGATACAGTCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:133395701..133395800 26863196 MeRIP-seq:(Medium) rs149301517 Functional Loss SNV dbSNP153 33..33 33 - - - 68371 RMVar_ID_68371 Human_SNP_ID_452727565 m1A Human chr10 - 133415873 133415843 133415873 ACGTGCCTGATACCGGCATGCCTGATAACTGCATGCCTGATACCCACCTGCCTGATACCCGCGTG ACGTGCCTGATACCGGCATGCCTGATAACTGC______________________________GTG CGCGGGTATCAGGCAGGTGGGTATCAGGCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133415840..133416075 26863196 MeRIP-seq:(Medium) rs1376484400 Functional Loss DEL dbSNP153 33..62 33 - - - 68372 RMVar_ID_68372 Human_SNP_ID_452727568 m1A Human chr10 - 133415860 133415845 133415860 CGGCATGCCTGATAACTGCATGCCTGATACCCACCTGCCTGATACCCGCGTGCCTGATACCTGCA CGGCATGCCTGATAACTGCATGCCTGATACCC_______________GCGTGCCTGATACCTGCA CGGGTATCAGGCAGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133415842..133416051 26863196 MeRIP-seq:(Medium) rs1410587468 Functional Loss DEL dbSNP153 33..47 33 - - - 68373 RMVar_ID_68373 Human_SNP_ID_452727571 m1A Human chr10 - 133415860 133415857 133415861 CGGCATGCCTGATAACTGCATGCCTGATACCCACCTGCCTGATACCCGCGTGCCTGATACCTGCA CGGCATGCCTGATAACTGCATGCCTGATACC____TGCCTGATACCCGCGTGCCTGATACCTGCA AGGTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133415842..133416051 26863196 MeRIP-seq:(Medium) rs1252265586 Functional Loss DEL dbSNP153 32..35 33 - - - 68374 RMVar_ID_68374 Human_SNP_ID_452730030 m1A Human chr10 + 133423055 133423055 133423055 ATGGTCTCCTCTAGGTGGGAGGTGGCAGGCTGAGGCGGCGTGGGCAGGACGGTGGATGGCGGGTC ATGGTCTCCTCTAGGTGGGAGGTGGCAGGCTGTGGCGGCGTGGGCAGGACGGTGGATGGCGGGTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:133422887..133423109;chr10:133422776..133423389 26863196 MeRIP-seq:(Medium) rs972205154 Functional Loss SNV dbSNP153 33..33 33 - - - 68375 RMVar_ID_68375 Human_SNP_ID_452730571 m1A Human chr10 + 133423725 133423722 133423726 TAAACCTGCGGGAAGAGAGGGAAAGGGCCCTTAGTTTCCATGGAGATCGGGTGCCCAGGGGCGGA TAAACCTGCGGGAAGAGAGGGAAAGGGCCC____TTTCCATGGAGATCGGGTGCCCAGGGGCGGA CTTAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:133423675..133423773 26863196 MeRIP-seq:(Medium) rs1342746514 Functional Loss DEL dbSNP153 31..34 33 - - - 68376 RMVar_ID_68376 Human_SNP_ID_452730573 m1A Human chr10 + 133423725 133423725 133423725 TAAACCTGCGGGAAGAGAGGGAAAGGGCCCTTAGTTTCCATGGAGATCGGGTGCCCAGGGGCGGA TAAACCTGCGGGAAGAGAGGGAAAGGGCCCTTGGTTTCCATGGAGATCGGGTGCCCAGGGGCGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:133423675..133423773 26863196 MeRIP-seq:(Medium) rs767266807 Functional Loss SNV dbSNP153 33..33 33 - - - 68377 RMVar_ID_68377 Human_SNP_ID_452730584 m1A Human chr10 + 133423749 133423748 133423749 GGGCCCTTAGTTTCCATGGAGATCGGGTGCCCAGGGGCGGAGGGCTCAAGGCTGGAGAGCAGAGG GGGCCCTTAGTTTCCATGGAGATCGGGTGCCC_GGGGCGGAGGGCTCAAGGCTGGAGAGCAGAGG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133423650..133423783 26863196 MeRIP-seq:(Medium) rs1157868122 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5948404,Human_RBP_ID_17773398 68378 RMVar_ID_68378 Human_SNP_ID_452731132 m1A Human chr10 + 133424823 133424822 133424823 CGCTCCACCCGCCGTGCTTCCTGCCCCTCCACACCCTCGTCCCCACCCGGGCCCATCCCCCTGTG CGCTCCACCCGCCGTGCTTCCTGCCCCTCCAC_CCCTCGTCCCCACCCGGGCCCATCCCCCTGTG CA C lnc-MTG1-2 RNACentral:URS0000D5772B lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:133424701..133425089 26863410 MeRIP-seq:(Medium) rs1340421097 Functional Loss DEL dbSNP153 33..33 33 - - - 68379 RMVar_ID_68379 Human_SNP_ID_452740532 m1A Human chr10 + 133460102 133460102 133460102 GGGCTGCCAGGGCCACGAGTCTGCGCTGTGGCAGTGCCCGTCGGCGGGCTGGGGGCGGCACGACT GGGCTGCCAGGGCCACGAGTCTGCGCTGTGGCGGTGCCCGTCGGCGGGCTGGGGGCGGCACGACT A G SCART1 Ensembl:ENSG00000214279 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133460091..133460156 26863196 MeRIP-seq:(Medium) rs1329365699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18477155,Human_RBP_ID_22886704,Human_RBP_ID_26774945,Human_RBP_ID_27836084 Human_Splice_Rec_1191589,Human_Splice_Rec_1191609,Human_Splice_Rec_1191631,Human_Splice_Rec_1191647 RMVar_hsa_circ_52330,RMVar_hsa_circ_328126 68380 RMVar_ID_68380 Human_SNP_ID_452740592 m1A Human chr10 + 133460285 133460284 133460285 CTATCGGGAGCTGTTCTCTTCCCTGAATGCAGAACTTCCACAGTGGATTGGGTGAGGTTCCTGTT CTATCGGGAGCTGTTCTCTTCCCTGAATGCAG_ACTTCCACAGTGGATTGGGTGAGGTTCCTGTT GA G SCART1 Ensembl:ENSG00000214279 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:133460268..133460368 32194978 MeRIP-seq:(Medium) rs1387905678 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11315470,Human_RBP_ID_22886705 RMVar_hsa_circ_328126 68381 RMVar_ID_68381 Human_SNP_ID_452742182 m1A Human chr10 - 133465630 133465630 133465630 GCGAGCTCTCCTGCCCACCGAAGTGACACTCAAGACTGACTCCATCCCAGCGCCCTCTGCCGGCC GCGAGCTCTCCTGCCCACCGAAGTGACACTCAGGACTGACTCCATCCCAGCGCCCTCTGCCGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:133465616..133465681 26863196 MeRIP-seq:(Medium) rs1303522600 Functional Loss SNV dbSNP153 33..33 33 - - - 68382 RMVar_ID_68382 Human_SNP_ID_452768999 m1A Human chr10 - 133569584 133569553 133569584 TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGGAGCCGGGTGCGGGGGTCGCGGGGGACCGCGGGG TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGG_______________________________GG CCCGCGGTCCCCCGCGACCCCCGCACCCGGCT C SYCE1 Ensembl:ENSG00000171772 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:133569536..133569649;chr10:133569536..133569708;chr10:133569536..133569642;chr10:133569528..133569654;chr10:133569525..133569655 26863196 MeRIP-seq:(Medium) rs1379255249 Functional Loss DEL dbSNP153 33..63 33 - - - 68383 RMVar_ID_68383 Human_SNP_ID_452769017 m1A Human chr10 - 133569584 133569584 133569584 TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGGAGCCGGGTGCGGGGGTCGCGGGGGACCGCGGGG TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGGGGCCGGGTGCGGGGGTCGCGGGGGACCGCGGGG T C SYCE1 Ensembl:ENSG00000171772 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:133569536..133569649;chr10:133569536..133569708;chr10:133569536..133569642;chr10:133569528..133569654;chr10:133569525..133569655 26863196 MeRIP-seq:(Medium) rs532152451 Functional Loss SNV dbSNP153 33..33 33 - - - 68384 RMVar_ID_68384 Human_SNP_ID_452769019 m1A Human chr10 + 133569592 133569592 133569592 TCCCCCGCGACCCCCGCACCCGGCTCCGCTCCACCCGCCGTGCTTCCTGCCCCTCCACACCCTCG TCCCCCGCGACCCCCGCACCCGGCTCCGCTCCGCCCGCCGTGCTTCCTGCCCCTCCACACCCTCG A G AL731769.2 Ensembl:ENSG00000288107 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:133569549..133569707 26863196 MeRIP-seq:(Medium) rs1198158073 Functional Loss SNV dbSNP153 33..33 33 - - - 68385 RMVar_ID_68385 Human_SNP_ID_474478931 m1A Human chr11 + 82689629 82689629 82689629 GGTCACCAAGGTCCTGGGCAGGACCGGTTCTCAGGGACAGTGCACGCAGGTGCGCGTGGAATTCA GGTCACCAAGGTCCTGGGCAGGACCGGTTCTCGGGGACAGTGCACGCAGGTGCGCGTGGAATTCA A G RPS28P7 Ensembl:ENSG00000227097 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:82689588..82689661 26863196 MeRIP-seq:(Medium) rs921701255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404737,Human_RBP_ID_1460698,Human_RBP_ID_1783025,Human_RBP_ID_4195074,Human_RBP_ID_6109803,Human_RBP_ID_8359924,Human_RBP_ID_9006806,Human_RBP_ID_17350865,Human_RBP_ID_17806080,Human_RBP_ID_18205981,Human_RBP_ID_18409238,Human_RBP_ID_18510898,Human_RBP_ID_18526156,Human_RBP_ID_23523557,Human_RBP_ID_26407434,Human_RBP_ID_26804020,Human_RBP_ID_26898114 Human_miRNA_ID_1820233,Human_miRNA_ID_1820362,Human_miRNA_ID_1873257,Human_miRNA_ID_1897509,Human_miRNA_ID_1903294 68386 RMVar_ID_68386 Human_SNP_ID_474478943 m1A Human chr11 - 82689662 82689662 82689662 CATTGCGGATGATGGATCGGCTCGTGTCGTCCATGAATTCCACGCGCACCTGCGTGCACTGTCCC CATTGCGGATGATGGATCGGCTCGTGTCGTCCCTGAATTCCACGCGCACCTGCGTGCACTGTCCC T G MIR4300HG Ensembl:ENSG00000245832 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:82689570..82689669 26863410 MeRIP-seq:(Medium) rs1205919795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4187035 68387 RMVar_ID_68387 Human_SNP_ID_474478993 m1A Human chr11 + 82689836 82689836 82689836 GACCACTTGGCCGATGGGAATGGTCTGTCACAATCTGCTCCTTTTTTTTGTCCGCCACACGTAAC GACCACTTGGCCGATGGGAATGGTCTGTCACAGTCTGCTCCTTTTTTTTGTCCGCCACACGTAAC A G lnc-DDIAS-6 RNACentral:URS00008C3757 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:82689776..82689900 32194978 MeRIP-seq:(Medium) rs878930453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404743,Human_RBP_ID_1080799,Human_RBP_ID_1355311,Human_RBP_ID_1460700,Human_RBP_ID_1783026,Human_RBP_ID_2287494,Human_RBP_ID_3381107,Human_RBP_ID_4180228,Human_RBP_ID_5273881,Human_RBP_ID_6098766,Human_RBP_ID_8359926,Human_RBP_ID_9006809,Human_RBP_ID_11729936,Human_RBP_ID_17184905,Human_RBP_ID_17233252,Human_RBP_ID_17349511,Human_RBP_ID_17466301,Human_RBP_ID_18613584,Human_RBP_ID_23523561,Human_RBP_ID_24462417,Human_RBP_ID_26410756,Human_RBP_ID_26606208,Human_RBP_ID_26898118,Human_RBP_ID_27207667 68388 RMVar_ID_68388 Human_SNP_ID_474478995 m1A Human chr11 - 82689839 82689839 82689839 TCAGTTACGTGTGGCGGACAAAAAAAAGGAGCAGATTGTGACAGACCATTCCCATCGGCCAAGTG TCAGTTACGTGTGGCGGACAAAAAAAAGGAGCGGATTGTGACAGACCATTCCCATCGGCCAAGTG T C MIR4300HG Ensembl:ENSG00000245832 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:82689776..82689900 26863196 MeRIP-seq:(Medium) rs1199522940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4187035 68389 RMVar_ID_68389 Human_SNP_ID_474512939 m1A Human chr11 - 82825113 82825113 82825113 TTTCTTCTTTTTTTCACTTGCAGCAATGGTGAACTAGACCCCTGGTCAGGAGGTGGAGTAACTAA TTTCTTCTTTTTTTCACTTGCAGCAATGGTGAGCTAGACCCCTGGTCAGGAGGTGGAGTAACTAA T C PRCP Ensembl:ENSG00000137509 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:82824901..82825152 32194978 MeRIP-seq:(Medium) rs1244177011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8229121,Human_RBP_ID_22753781 Human_Splice_Rec_1282658,Human_Splice_Rec_1282676,Human_Splice_Rec_1282680,Human_Splice_Rec_1282686 RMVar_hsa_circ_85870,RMVar_hsa_circ_109821,RMVar_hsa_circ_152127,RMVar_hsa_circ_81966,RMVar_hsa_circ_152128,RMVar_hsa_circ_152126 68390 RMVar_ID_68390 Human_SNP_ID_474521579 m1A Human chr11 - 82860113 82860113 82860113 AATATGTTTTGTTTTGTTTTTATCACAGGTTGATCATTTTGGATTTAATACTGTGAAAACTTTTA AATATGTTTTGTTTTGTTTTTATCACAGGTTGGTCATTTTGGATTTAATACTGTGAAAACTTTTA T C PRCP Ensembl:ENSG00000137509 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:82860024..82884830 32194978 MeRIP-seq:(Medium) rs1207315748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1282644,Human_Splice_Rec_1282662,Human_Splice_Rec_1282702,Human_Splice_Rec_1282722,Human_Splice_Rec_1282742,Human_Splice_Rec_1282750,Human_Splice_Rec_1282758,Human_Splice_Rec_1282766,Human_Splice_Rec_1282772 RMVar_hsa_circ_81966,RMVar_hsa_circ_152128,RMVar_hsa_circ_323256,RMVar_hsa_circ_152129,RMVar_hsa_circ_152132,RMVar_hsa_circ_298213 68391 RMVar_ID_68391 Human_SNP_ID_474530996 m1A Human chr11 + 82900366 82900366 82900366 CCGGAGGGCTATGGTGGCCCAGGGCGCCAGAAAAGACAGAAGCAGGAGCAGGAGGGCTCGGCGGC CCGGAGGGCTATGGTGGCCCAGGGCGCCAGAAGAGACAGAAGCAGGAGCAGGAGGGCTCGGCGGC A G DDIAS Ensembl:ENSG00000165490 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:82900276..82900425 26863410 MeRIP-seq:(Medium) rs1274393921 Functional Loss SNV dbSNP153 33..33 33 - - - 68392 RMVar_ID_68392 Human_SNP_ID_474566005 m1A Human chr11 + 83055463 83055463 83055463 TCACTGTTCCCTTCCCCTGAGTTGCCCTTCTCACCTTCCTCATTGACACACAAATTTTATCCATC TCACTGTTCCCTTCCCCTGAGTTGCCCTTCTCGCCTTCCTCATTGACACACAAATTTTATCCATC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:83055436..83055522 26863196 MeRIP-seq:(Medium) rs941738830 Functional Loss SNV dbSNP153 33..33 33 - - - 68393 RMVar_ID_68393 Human_SNP_ID_474569969 m1A Human chr11 + 83072683 83072683 83072683 TCGTTGTTGGAAGGTGACCAAGGTGGAAAGAGACGTTGCTTTGGCCCTGCAAGTAAGAAGAGAGA TCGTTGTTGGAAGGTGACCAAGGTGGAAAGAGGCGTTGCTTTGGCCCTGCAAGTAAGAAGAGAGA A G RAB30-DT Ensembl:ENSG00000246067 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:83072672..83072772 26863410 MeRIP-seq:(Medium) rs956246399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868955,Human_RBP_ID_1460720,Human_RBP_ID_2287669,Human_RBP_ID_4187038,Human_RBP_ID_5093164,Human_RBP_ID_6098963,Human_RBP_ID_11730351 Human_Splice_Rec_1282982,Human_Splice_Rec_1282986,Human_Splice_Rec_1282990,Human_Splice_Rec_1282996,Human_Splice_Rec_1282998,Human_Splice_Rec_1283004,Human_Splice_Rec_1283012,Human_Splice_Rec_1283014,Human_Splice_Rec_1283017 Human_miRNA_ID_3175285,Human_miRNA_ID_3183607 RMVar_hsa_circ_41903,RMVar_hsa_circ_351397 68394 RMVar_ID_68394 Human_SNP_ID_474574183 m1A Human chr11 - 83089122 83089122 83089122 CCTCCTTAAGCCTTCAATCCCATCCTCTATCTAATCAAACACACACACCCTTTACCTTTTCTGAG CCTCCTTAAGCCTTCAATCCCATCCTCTATCTGATCAAACACACACACCCTTTACCTTTTCTGAG T C AP001767.3 Ensembl:ENSG00000255503 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:83089084..83089220 26863196 MeRIP-seq:(Medium) rs145417679 Functional Loss SNV dbSNP153 33..33 33 - - - 68395 RMVar_ID_68395 Human_SNP_ID_474574184 m1A Human chr11 - 83089122 83089122 83089122 CCTCCTTAAGCCTTCAATCCCATCCTCTATCTAATCAAACACACACACCCTTTACCTTTTCTGAG CCTCCTTAAGCCTTCAATCCCATCCTCTATCTCATCAAACACACACACCCTTTACCTTTTCTGAG T G AP001767.3 Ensembl:ENSG00000255503 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:83089084..83089220 26863196 MeRIP-seq:(Medium) rs145417679 Functional Loss SNV dbSNP153 33..33 33 - - - 68396 RMVar_ID_68396 Human_SNP_ID_474591519 m1A Human chr11 + 83157247 83157247 83157247 GCTTCTGTGGCGGCTGGAAGTGGACGGAGATCACCCGCGAGACGGCGGCGTTTCATACCCGAGGT GCTTCTGTGGCGGCTGGAAGTGGACGGAGATCTCCCGCGAGACGGCGGCGTTTCATACCCGAGGT A T PCF11 Ensembl:ENSG00000165494 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:83157201..83157487 26863196 MeRIP-seq:(Medium) rs888110928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31138,Human_RBP_ID_868245,Human_RBP_ID_5490467,Human_RBP_ID_9321753,Human_RBP_ID_9364203,Human_RBP_ID_11731162,Human_RBP_ID_18416636,Human_RBP_ID_22034852,Human_RBP_ID_22895206,Human_RBP_ID_26317855,Human_RBP_ID_26898186,Human_RBP_ID_27803888 RMVar_hsa_circ_108932,RMVar_hsa_circ_152141 68397 RMVar_ID_68397 Human_SNP_ID_474601425 m1A Human chr11 - 83193526 83193526 83193526 CCTATCTAGGTCCGTCTCTGGAGTGGCCTGTCATCGATCGCGCCCTCCATCGCTGAGCGACACAA CCTATCTAGGTCCGTCTCTGGAGTGGCCTGTCTTCGATCGCGCCCTCCATCGCTGAGCGACACAA T A AP000873.2 Ensembl:ENSG00000247137 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:83193482..83193584 26863196 MeRIP-seq:(Medium) rs747464998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362818,Human_RBP_ID_11731630,Human_RBP_ID_22167682,Human_RBP_ID_22895475,Human_RBP_ID_23523852 Human_Splice_Rec_1283111,Human_Splice_Rec_1283117,Human_Splice_Rec_1283119,Human_Splice_Rec_1283129,Human_Splice_Rec_1283135,Human_Splice_Rec_1283141,Human_Splice_Rec_1283147,Human_Splice_Rec_1283149 RMVar_hsa_circ_96614,RMVar_hsa_circ_119892,RMVar_hsa_circ_152157,RMVar_hsa_circ_152158 68398 RMVar_ID_68398 Human_SNP_ID_474601426 m1A Human chr11 - 83193526 83193526 83193526 CCTATCTAGGTCCGTCTCTGGAGTGGCCTGTCATCGATCGCGCCCTCCATCGCTGAGCGACACAA CCTATCTAGGTCCGTCTCTGGAGTGGCCTGTCGTCGATCGCGCCCTCCATCGCTGAGCGACACAA T C AP000873.2 Ensembl:ENSG00000247137 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:83193482..83193584 26863196 MeRIP-seq:(Medium) rs747464998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362818,Human_RBP_ID_11731630,Human_RBP_ID_22167682,Human_RBP_ID_22895475,Human_RBP_ID_23523852 Human_Splice_Rec_1283111,Human_Splice_Rec_1283117,Human_Splice_Rec_1283119,Human_Splice_Rec_1283129,Human_Splice_Rec_1283135,Human_Splice_Rec_1283141,Human_Splice_Rec_1283147,Human_Splice_Rec_1283149 RMVar_hsa_circ_96614,RMVar_hsa_circ_119892,RMVar_hsa_circ_152157,RMVar_hsa_circ_152158 68399 RMVar_ID_68399 Human_SNP_ID_474601597 m1A Human chr11 + 83193839 83193839 83193839 GGCCGCCGCTACGGCGATTCGCAGGGAGTAGCAGACGAAGACGGTGGCCGCCGCACTAGCCACCA GGCCGCCGCTACGGCGATTCGCAGGGAGTAGCCGACGAAGACGGTGGCCGCCGCACTAGCCACCA A C ANKRD42 Ensembl:ENSG00000137494 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:83193788..83194200 26863196 MeRIP-seq:(Medium) rs1426742772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185311 68400 RMVar_ID_68400 Human_SNP_ID_475205111 m1A Human chr11 + 85484110 85484110 85484110 GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTACAAGAGGGCGTGAAACCGTTAAGAGGTAAATG GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTGCAAGAGGGCGTGAAACCGTTAAGAGGTAAATG A G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c chr11:85483923..85484138 31548705,26863196 m1A-IP-seq:(High) rs4943920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269370,Human_RBP_ID_274754,Human_RBP_ID_407541,Human_RBP_ID_988597,Human_RBP_ID_1080809,Human_RBP_ID_1126314,Human_RBP_ID_1163695,Human_RBP_ID_1266479,Human_RBP_ID_1355340,Human_RBP_ID_1460789,Human_RBP_ID_1783212,Human_RBP_ID_2288750,Human_RBP_ID_3381471,Human_RBP_ID_4180757,Human_RBP_ID_5165775,Human_RBP_ID_5273771,Human_RBP_ID_5416414,Human_RBP_ID_5436994,Human_RBP_ID_5460919,Human_RBP_ID_5490486,Human_RBP_ID_5550310,Human_RBP_ID_6099833,Human_RBP_ID_8065206,Human_RBP_ID_8246589,Human_RBP_ID_8360232,Human_RBP_ID_8772194,Human_RBP_ID_9007448,Human_RBP_ID_9275194,Human_RBP_ID_9649802,Human_RBP_ID_10482337,Human_RBP_ID_11732219,Human_RBP_ID_16988134,Human_RBP_ID_17062361,Human_RBP_ID_17067119,Human_RBP_ID_17108855,Human_RBP_ID_17184918,Human_RBP_ID_17233287,Human_RBP_ID_17349546,Human_RBP_ID_17466351,Human_RBP_ID_17682743,Human_RBP_ID_17806510,Human_RBP_ID_18176556,Human_RBP_ID_18198780,Human_RBP_ID_18205933,Human_RBP_ID_18252749,Human_RBP_ID_18433266,Human_RBP_ID_18510800,Human_RBP_ID_18526386,Human_RBP_ID_18613774,Human_RBP_ID_19583612,Human_RBP_ID_21916183,Human_RBP_ID_22167734,Human_RBP_ID_22381455,Human_RBP_ID_22420775,Human_RBP_ID_22491904,Human_RBP_ID_22792370,Human_RBP_ID_22894258,Human_RBP_ID_23124855,Human_RBP_ID_23155198,Human_RBP_ID_23267411,Human_RBP_ID_23305516,Human_RBP_ID_23524281,Human_RBP_ID_24404522,Human_RBP_ID_24462450,Human_RBP_ID_24905710,Human_RBP_ID_26407604,Human_RBP_ID_26606351,Human_RBP_ID_26747738,Human_RBP_ID_26898389,Human_RBP_ID_27154505,Human_RBP_ID_27208771,Human_RBP_ID_27416609,Human_RBP_ID_27620106 68401 RMVar_ID_68401 Human_SNP_ID_475205112 m1A Human chr11 + 85484110 85484110 85484110 GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTACAAGAGGGCGTGAAACCGTTAAGAGGTAAATG GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTTCAAGAGGGCGTGAAACCGTTAAGAGGTAAATG A T - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c chr11:85483923..85484138 31548705,26863196 m1A-IP-seq:(High) rs4943920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269370,Human_RBP_ID_274754,Human_RBP_ID_407541,Human_RBP_ID_988597,Human_RBP_ID_1080809,Human_RBP_ID_1126314,Human_RBP_ID_1163695,Human_RBP_ID_1266479,Human_RBP_ID_1355340,Human_RBP_ID_1460789,Human_RBP_ID_1783212,Human_RBP_ID_2288750,Human_RBP_ID_3381471,Human_RBP_ID_4180757,Human_RBP_ID_5165775,Human_RBP_ID_5273771,Human_RBP_ID_5416414,Human_RBP_ID_5436994,Human_RBP_ID_5460919,Human_RBP_ID_5490486,Human_RBP_ID_5550310,Human_RBP_ID_6099833,Human_RBP_ID_8065206,Human_RBP_ID_8246589,Human_RBP_ID_8360232,Human_RBP_ID_8772194,Human_RBP_ID_9007448,Human_RBP_ID_9275194,Human_RBP_ID_9649802,Human_RBP_ID_10482337,Human_RBP_ID_11732219,Human_RBP_ID_16988134,Human_RBP_ID_17062361,Human_RBP_ID_17067119,Human_RBP_ID_17108855,Human_RBP_ID_17184918,Human_RBP_ID_17233287,Human_RBP_ID_17349546,Human_RBP_ID_17466351,Human_RBP_ID_17682743,Human_RBP_ID_17806510,Human_RBP_ID_18176556,Human_RBP_ID_18198780,Human_RBP_ID_18205933,Human_RBP_ID_18252749,Human_RBP_ID_18433266,Human_RBP_ID_18510800,Human_RBP_ID_18526386,Human_RBP_ID_18613774,Human_RBP_ID_19583612,Human_RBP_ID_21916183,Human_RBP_ID_22167734,Human_RBP_ID_22381455,Human_RBP_ID_22420775,Human_RBP_ID_22491904,Human_RBP_ID_22792370,Human_RBP_ID_22894258,Human_RBP_ID_23124855,Human_RBP_ID_23155198,Human_RBP_ID_23267411,Human_RBP_ID_23305516,Human_RBP_ID_23524281,Human_RBP_ID_24404522,Human_RBP_ID_24462450,Human_RBP_ID_24905710,Human_RBP_ID_26407604,Human_RBP_ID_26606351,Human_RBP_ID_26747738,Human_RBP_ID_26898389,Human_RBP_ID_27154505,Human_RBP_ID_27208771,Human_RBP_ID_27416609,Human_RBP_ID_27620106 68402 RMVar_ID_68402 Human_SNP_ID_475205113 m1A Human chr11 + 85484112 85484112 85484112 GAAAGTTGAAAAGAACTTTGAAGAGAGAGTACAAGAGGGCGTGAAACCGTTAAGAGGTAAATGGG GAAAGTTGAAAAGAACTTTGAAGAGAGAGTACGAGAGGGCGTGAAACCGTTAAGAGGTAAATGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:85483973..85484266 26863196 MeRIP-seq:(Medium) rs1455898529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269370,Human_RBP_ID_274754,Human_RBP_ID_405025,Human_RBP_ID_988597,Human_RBP_ID_1080809,Human_RBP_ID_1126314,Human_RBP_ID_1163695,Human_RBP_ID_1266479,Human_RBP_ID_1355340,Human_RBP_ID_1460789,Human_RBP_ID_1783212,Human_RBP_ID_2288750,Human_RBP_ID_3381471,Human_RBP_ID_4180757,Human_RBP_ID_5165775,Human_RBP_ID_5273771,Human_RBP_ID_5416414,Human_RBP_ID_5436994,Human_RBP_ID_5460919,Human_RBP_ID_5490486,Human_RBP_ID_5550310,Human_RBP_ID_6099833,Human_RBP_ID_8065206,Human_RBP_ID_8246589,Human_RBP_ID_8360232,Human_RBP_ID_8772194,Human_RBP_ID_9007448,Human_RBP_ID_9275194,Human_RBP_ID_9649802,Human_RBP_ID_10482337,Human_RBP_ID_11732219,Human_RBP_ID_16988134,Human_RBP_ID_17062361,Human_RBP_ID_17067119,Human_RBP_ID_17108855,Human_RBP_ID_17184918,Human_RBP_ID_17233287,Human_RBP_ID_17349546,Human_RBP_ID_17466351,Human_RBP_ID_17682743,Human_RBP_ID_17802374,Human_RBP_ID_18176556,Human_RBP_ID_18198780,Human_RBP_ID_18205933,Human_RBP_ID_18252749,Human_RBP_ID_18433266,Human_RBP_ID_18510800,Human_RBP_ID_18526386,Human_RBP_ID_18613774,Human_RBP_ID_19583612,Human_RBP_ID_21916183,Human_RBP_ID_22167734,Human_RBP_ID_22381455,Human_RBP_ID_22420775,Human_RBP_ID_22491904,Human_RBP_ID_22792370,Human_RBP_ID_22894258,Human_RBP_ID_23124855,Human_RBP_ID_23155198,Human_RBP_ID_23267411,Human_RBP_ID_23305516,Human_RBP_ID_23524281,Human_RBP_ID_24404522,Human_RBP_ID_24462450,Human_RBP_ID_24529479,Human_RBP_ID_24905710,Human_RBP_ID_26407604,Human_RBP_ID_26606351,Human_RBP_ID_26747738,Human_RBP_ID_26898389,Human_RBP_ID_27154505,Human_RBP_ID_27207832,Human_RBP_ID_27416609,Human_RBP_ID_27620106 68403 RMVar_ID_68403 Human_SNP_ID_475205192 m1A Human chr11 + 85484214 85484214 85484214 TGGCGGATCTTTCCCGCCCCCCGTTCCTCCCGACCCCTCCACCCGCCCTCCCTCTCCCACCGCCC TGGCGGATCTTTCCCGCCCCCCGTTCCTCCCGCCCCCTCCACCCGCCCTCCCTCTCCCACCGCCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:85483921..85484321 26863196 MeRIP-seq:(Medium) rs1439508818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269370,Human_RBP_ID_274757,Human_RBP_ID_405026,Human_RBP_ID_1266075,Human_RBP_ID_1355348,Human_RBP_ID_1460793,Human_RBP_ID_2296523,Human_RBP_ID_4195193,Human_RBP_ID_5170284,Human_RBP_ID_5416423,Human_RBP_ID_5437003,Human_RBP_ID_5460928,Human_RBP_ID_5490495,Human_RBP_ID_6099837,Human_RBP_ID_8065206,Human_RBP_ID_8246597,Human_RBP_ID_8360232,Human_RBP_ID_8774858,Human_RBP_ID_9254439,Human_RBP_ID_9275194,Human_RBP_ID_11732220,Human_RBP_ID_16987592,Human_RBP_ID_17233287,Human_RBP_ID_17349546,Human_RBP_ID_17466351,Human_RBP_ID_17682743,Human_RBP_ID_17802378,Human_RBP_ID_18198789,Human_RBP_ID_18205939,Human_RBP_ID_18252750,Human_RBP_ID_18433266,Human_RBP_ID_18613775,Human_RBP_ID_19583614,Human_RBP_ID_21916183,Human_RBP_ID_22167734,Human_RBP_ID_22420775,Human_RBP_ID_22491904,Human_RBP_ID_22792370,Human_RBP_ID_22894260,Human_RBP_ID_23155198,Human_RBP_ID_23268060,Human_RBP_ID_23305521,Human_RBP_ID_23524292,Human_RBP_ID_24404525,Human_RBP_ID_24462455,Human_RBP_ID_24529481,Human_RBP_ID_24538505,Human_RBP_ID_24539693,Human_RBP_ID_24905724,Human_RBP_ID_26407614,Human_RBP_ID_26606351,Human_RBP_ID_26747740,Human_RBP_ID_26898389,Human_RBP_ID_27154509,Human_RBP_ID_27207836,Human_RBP_ID_27416625,Human_RBP_ID_27557453 Human_miRNA_ID_2153380,Human_miRNA_ID_2690067,Human_miRNA_ID_2693324,Human_miRNA_ID_2801259,Human_miRNA_ID_3009389 68404 RMVar_ID_68404 Human_SNP_ID_475250185 m1A Human chr11 - 85647993 85647984 85647994 GTGGCCTTTGCTCAAATTACCTGGGCGCAGCCATCTTTGGCTGACTCGTGACGCGGCGTGGGCGG GTGGCCTTTGCTCAAATTACCTGGGCGCAGC__________TGACTCGTGACGCGGCGTGGGCGG AGCCAAAGATG A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:85647975..85648101 26863196 MeRIP-seq:(Medium) rs1488543860 Functional Loss DEL dbSNP153 32..41 33 - - - 68405 RMVar_ID_68405 Human_SNP_ID_475250201 m1A Human chr11 + 85648026 85648026 85648026 GGCTGCGCCCAGGTAATTTGAGCAAAGGCCACAGTGAACTCCGGCGTGGCTGAGGAAGGAGGAGG GGCTGCGCCCAGGTAATTTGAGCAAAGGCCACGGTGAACTCCGGCGTGGCTGAGGAAGGAGGAGG A G TMEM126A Ensembl:ENSG00000171202 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:85647976..85648137 26863196 MeRIP-seq:(Medium) rs1330545695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185314 Human_Splice_Rec_1284297,Human_Splice_Rec_1284305,Human_Splice_Rec_1284313,Human_Splice_Rec_1284319,Human_Splice_Rec_1284327 68406 RMVar_ID_68406 Human_SNP_ID_475250812 m1A Human chr11 - 85650271 85650271 85650271 ATCAACAATTGTTATGTTTTCCTTATTATTGGATTTATGATTTTCCATTTTGAGCCTTAAAAAAC ATCAACAATTGTTATGTTTTCCTTATTATTGGGTTTATGATTTTCCATTTTGAGCCTTAAAAAAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:85648063..85654164 32194978 MeRIP-seq:(Medium) rs1279650258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24905852 68407 RMVar_ID_68407 Human_SNP_ID_475254467 m1A Human chr11 - 85664274 85664272 85664275 AGGAGGAGGCGGCGGTGGCGGCAGCGGTAACGACAACAACCAGGCGGCGACAAAGAGTCCCCGGA AGGAGGAGGCGGCGGTGGCGGCAGCGGTAAC___AACAACCAGGCGGCGACAAAGAGTCCCCGGA TGTC T CREBZF Ensembl:ENSG00000137504 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:85664003..85665045 26863196 MeRIP-seq:(Medium) rs767444290 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5520913,Human_RBP_ID_17802468 68408 RMVar_ID_68408 Human_SNP_ID_475254505 m1A Human chr11 - 85664347 85664345 85664348 TGTTAAACGGTATCGGAGGCTGCAGCAGCAGCAGTGACAGTGGCAGCGCCGAAAAGAGGCGGAGA TGTTAAACGGTATCGGAGGCTGCAGCAGCAG___TGACAGTGGCAGCGCCGAAAAGAGGCGGAGA ACTG A CREBZF Ensembl:ENSG00000137504 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:85664156..85664375 26863196 MeRIP-seq:(Medium) rs760647744 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_988661,Human_RBP_ID_11732904 68409 RMVar_ID_68409 Human_SNP_ID_475254508 m1A Human chr11 - 85664347 85664347 85664347 TGTTAAACGGTATCGGAGGCTGCAGCAGCAGCAGTGACAGTGGCAGCGCCGAAAAGAGGCGGAGA TGTTAAACGGTATCGGAGGCTGCAGCAGCAGCTGTGACAGTGGCAGCGCCGAAAAGAGGCGGAGA T A CREBZF Ensembl:ENSG00000137504 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:85664156..85664375 26863196 MeRIP-seq:(Medium) rs776857952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_988661,Human_RBP_ID_11732904 68410 RMVar_ID_68410 Human_SNP_ID_475254565 m1A Human chr11 + 85664482 85664480 85664483 CAGGCCGCCGCTATCCGAGCCTCCGCCAGACGAGGAGAGAGGCCCCGGCGAGCTAAGCCCGGGGT CAGGCCGCCGCTATCCGAGCCTCCGCCAGAC___GAGAGAGGCCCCGGCGAGCTAAGCCCGGGGT CGAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:85664345..85664745 32194978 MeRIP-seq:(Medium) rs1283020157 Functional Loss DEL dbSNP153 32..34 33 - - - 68411 RMVar_ID_68411 Human_SNP_ID_475254566 m1A Human chr11 + 85664482 85664482 85664482 CAGGCCGCCGCTATCCGAGCCTCCGCCAGACGAGGAGAGAGGCCCCGGCGAGCTAAGCCCGGGGT CAGGCCGCCGCTATCCGAGCCTCCGCCAGACGTGGAGAGAGGCCCCGGCGAGCTAAGCCCGGGGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:85664345..85664745 32194978 MeRIP-seq:(Medium) rs1036872732 Functional Loss SNV dbSNP153 33..33 33 - - - 68412 RMVar_ID_68412 Human_SNP_ID_475404574 m1A Human chr11 - 86244791 86244791 86244791 GACGTTTCAGCCGCAATTGGCCCGTTCCTTCGATCTCCGACCCGCTGCTAGGGAGCGAAAGTCTG GACGTTTCAGCCGCAATTGGCCCGTTCCTTCGCTCTCCGACCCGCTGCTAGGGAGCGAAAGTCTG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:86244789..86244925 26863196 MeRIP-seq:(Medium) rs971571071 Functional Loss SNV dbSNP153 33..33 33 - - - 68413 RMVar_ID_68413 Human_SNP_ID_475404863 m1A Human chr11 + 86245272 86245272 86245272 GGGAAGTGTCGACTGCGCCGGCGGGAACAGACATGCCTGCGGCCAAGAAGCAGAAGCTGAGCAGT GGGAAGTGTCGACTGCGCCGGCGGGAACAGACGTGCCTGCGGCCAAGAAGCAGAAGCTGAGCAGT A G EED Ensembl:ENSG00000074266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:86244792..86245350;chr11:86244792..86250342 26863196 MeRIP-seq:(Medium) rs200782451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868263,Human_RBP_ID_18974849,Human_RBP_ID_22433224 Human_Splice_Rec_1285341,Human_Splice_Rec_1285359,Human_Splice_Rec_1285381,Human_Splice_Rec_1285403,Human_Splice_Rec_1285425,Human_Splice_Rec_1285445,Human_Splice_Rec_1285469,Human_Splice_Rec_1285473 Human_miRNA_ID_2979322 68414 RMVar_ID_68414 Human_SNP_ID_475419170 m1A Human chr11 + 86302319 86302319 86302319 GGGGCAGAGGCATTCTTGCCGCTGGCCCAGTCACTATGTAGTGGAGGGGCAGACACCCTCCCGCA GGGGCAGAGGCATTCTTGCCGCTGGCCCAGTCGCTATGTAGTGGAGGGGCAGACACCCTCCCGCA A G HIKESHI Ensembl:ENSG00000149196 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs291241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_405364,Human_RBP_ID_4181034,Human_RBP_ID_9321760,Human_RBP_ID_18417011,Human_RBP_ID_22435596 Human_miRNA_ID_2037328,Human_miRNA_ID_2151534,Human_miRNA_ID_2348032 GWAS_ID_8218,GWAS_ID_8219,GWAS_ID_8220,GWAS_ID_8221,GWAS_ID_8222,GWAS_ID_8223,GWAS_ID_8224 68415 RMVar_ID_68415 Human_SNP_ID_475547385 m1A Human chr11 - 86807694 86807694 86807694 CAGGGGGCACTGTAAGGGCTCACTTGCCCAACAGCACAGAGCAGAAAGAAGAGAAGGAAGAGGAG CAGGGGGCACTGTAAGGGCTCACTTGCCCAACGGCACAGAGCAGAAAGAAGAGAAGGAAGAGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:86807626..86807850 32194978 MeRIP-seq:(Medium) rs1358555589 Functional Loss SNV dbSNP153 33..33 33 - - - 68416 RMVar_ID_68416 Human_SNP_ID_475547544 m1A Human chr11 + 86808082 86808082 86808082 GGTTCAGCATTTTTGGGAAGGACTTCCTGCTCAACTACCCTTTCTCAACATCAGTGAAGTTATCC GGTTCAGCATTTTTGGGAAGGACTTCCTGCTCTACTACCCTTTCTCAACATCAGTGAAGTTATCC A T PRSS23 Ensembl:ENSG00000150687 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:86807901..86808200 32194978 MeRIP-seq:(Medium) rs1365440775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8360622,Human_RBP_ID_9007698,Human_RBP_ID_17233351,Human_RBP_ID_17349600,Human_RBP_ID_17802637,Human_RBP_ID_26898545,Human_RBP_ID_27416727 RMVar_hsa_circ_97572,RMVar_hsa_circ_152347 68417 RMVar_ID_68417 Human_SNP_ID_475577530 m1A Human chr11 + 86921015 86921015 86921015 TCTTGGCTTCCATGACACCCACTCTCCTATTCATGCTCCAGGTTCACTGTCTGCTCCTTCCTGGT TCTTGGCTTCCATGACACCCACTCTCCTATTCGTGCTCCAGGTTCACTGTCTGCTCCTTCCTGGT A G PRSS23 Ensembl:ENSG00000150687 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:86920944..86921040 26863196 MeRIP-seq:(Medium) rs999391100 Functional Loss SNV dbSNP153 33..33 33 - - - 68418 RMVar_ID_68418 Human_SNP_ID_475606861 m1A Human chr11 + 87038046 87038046 87038046 CCCCTCCTGTCTTCTCCGCGCTGTTCCTCGTCATGGCGGCCCTCAGCAAGTCCATCCCTCATAAC CCCCTCCTGTCTTCTCCGCGCTGTTCCTCGTCCTGGCGGCCCTCAGCAAGTCCATCCCTCATAAC A C TMEM135 Ensembl:ENSG00000166575 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:87037953..87038143 26863196 MeRIP-seq:(Medium) rs764863470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186275,Human_RBP_ID_17350324 RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_88108,RMVar_hsa_circ_152350 68419 RMVar_ID_68419 Human_SNP_ID_475606862 m1A Human chr11 + 87038046 87038046 87038046 CCCCTCCTGTCTTCTCCGCGCTGTTCCTCGTCATGGCGGCCCTCAGCAAGTCCATCCCTCATAAC CCCCTCCTGTCTTCTCCGCGCTGTTCCTCGTCGTGGCGGCCCTCAGCAAGTCCATCCCTCATAAC A G TMEM135 Ensembl:ENSG00000166575 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:87037953..87038143 26863196 MeRIP-seq:(Medium) rs764863470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186275,Human_RBP_ID_17350324 RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_88108,RMVar_hsa_circ_152350 68420 RMVar_ID_68420 Human_SNP_ID_475959318 m1A Human chr11 + 88337692 88337692 88337692 GCCCAGCACCCATGCTGCAGGGAGCTGAGAAAAGAGGTGAAGAATTACCAGGAAGCCGAGCGCTG GCCCAGCACCCATGCTGCAGGGAGCTGAGAAAGGAGGTGAAGAATTACCAGGAAGCCGAGCGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:88337567..88337725 26863196 MeRIP-seq:(Medium) rs1292437160 Functional Loss SNV dbSNP153 33..33 33 - - - 68421 RMVar_ID_68421 Human_SNP_ID_569451338 m1A Human chr15 - 20105135 20105135 20105135 CAAAGCCAGACAGCCACCCAGCCAGCCAAGCCAGTCAAGCCACCCAGCCAGCCAAGCCAGCCAAG CAAAGCCAGACAGCCACCCAGCCAGCCAAGCCGGTCAAGCCACCCAGCCAGCCAAGCCAGCCAAG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:20105133..20105217 26863410 MeRIP-seq:(Medium) rs1215388616 Functional Loss SNV dbSNP153 33..33 33 - - - 68422 RMVar_ID_68422 Human_SNP_ID_569550047 m1A Human chr15 - 20377006 20377006 20377006 ACACACAAGGCCACGGCACTGCAGTCATCAACAGAGCTCTGCCCAGGGATAGAATTGATGGAGAA ACACACAAGGCCACGGCACTGCAGTCATCAACCGAGCTCTGCCCAGGGATAGAATTGATGGAGAA T G RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:20376996..20377064 26863196 MeRIP-seq:(Medium) rs1455218530 Functional Loss SNV dbSNP153 33..33 33 - - - 68423 RMVar_ID_68423 Human_SNP_ID_569571492 m1A Human chr15 - 20442024 20442024 20442024 GTGTGAGTGTGAGGGGATTACTGGGTGTGCAAATGAGACACCCAGTGTAAGTGTAAGTCAGTGAG GTGTGAGTGTGAGGGGATTACTGGGTGTGCAAGTGAGACACCCAGTGTAAGTGTAAGTCAGTGAG T C HERC2P3 Ensembl:ENSG00000180229 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:20441991..20442062;chr15:20441973..20442069 26863196 MeRIP-seq:(Medium) rs541286101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5646120 RMVar_hsa_circ_94307,RMVar_hsa_circ_169971,RMVar_hsa_circ_99520,RMVar_hsa_circ_169972,RMVar_hsa_circ_114847,RMVar_hsa_circ_123310,RMVar_hsa_circ_169974,RMVar_hsa_circ_169975 68424 RMVar_ID_68424 Human_SNP_ID_569585258 m1A Human chr15 + 20506150 20506150 20506150 GGGCCCGGCCGCCCCGCCCCGCCGGCGCGCGGACGCAGCCTCCCAAGAGCCGCTGGCTCAGCCGG GGGCCCGGCCGCCCCGCCCCGCCGGCGCGCGGGCGCAGCCTCCCAAGAGCCGCTGGCTCAGCCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:20506065..20506158 26863196 MeRIP-seq:(Medium) rs1288725961 Functional Loss SNV dbSNP153 33..33 33 - - - 68425 RMVar_ID_68425 Human_SNP_ID_569718614 m1A Human chr15 + 21154683 21154682 21154684 CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGG CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGG__AGCGGCGGCGCGGCGGAGAGGCGGACAGCGG GAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:21154654..21154725 26863196 MeRIP-seq:(Medium) rs1253231681 Functional Loss DEL dbSNP153 33..34 33 - - - 68426 RMVar_ID_68426 Human_SNP_ID_569718615 m1A Human chr15 + 21154683 21154683 21154683 CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGG CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGGCCAGCGGCGGCGCGGCGGAGAGGCGGACAGCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:21154654..21154725 26863196 MeRIP-seq:(Medium) rs868840981 Functional Loss SNV dbSNP153 33..33 33 - - - 68427 RMVar_ID_68427 Human_SNP_ID_569718616 m1A Human chr15 + 21154683 21154683 21154683 CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGG CGGCGGAGAGGCGGACAGCGGCGGCGCGGCGGGCAGCGGCGGCGCGGCGGAGAGGCGGACAGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:21154654..21154725 26863196 MeRIP-seq:(Medium) rs868840981 Functional Loss SNV dbSNP153 33..33 33 - - - 68428 RMVar_ID_68428 Human_SNP_ID_569720781 m1A Human chr15 + 21165524 21165524 21165524 ACCAACTTTAAAGTTTTGGATTGCTTTTGTCAAACCACTGGGTTGCAAGTTCAGATGGTCTCTCT ACCAACTTTAAAGTTTTGGATTGCTTTTGTCAGACCACTGGGTTGCAAGTTCAGATGGTCTCTCT A G BMS1P16 Ensembl:ENSG00000258684 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1401971564 Functional Loss SNV dbSNP153 33..33 33 - - - 68429 RMVar_ID_68429 Human_SNP_ID_569964964 m1A Human chr15 + 22494932 22494932 22494932 TTGGGAGGCTGCGTCCGCGCGCCGGCGGGGCGAGGCGGCCGGGCCCTGCGCGTCAGGTCCTGGCC TTGGGAGGCTGCGTCCGCGCGCCGGCGGGGCGCGGCGGCCGGGCCCTGCGCGTCAGGTCCTGGCC A C lnc-GOLGA6L22-3,lnc-GOLGA6L22-3:2 RNACentral:URS00008B995D,RNACentral:URS00008BBE5E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:22494901..22494978;chr15:22494898..22494978 26863196 MeRIP-seq:(Medium) rs1260422069 Functional Loss SNV dbSNP153 33..33 33 - - - 68430 RMVar_ID_68430 Human_SNP_ID_569964965 m1A Human chr15 + 22494932 22494932 22494932 TTGGGAGGCTGCGTCCGCGCGCCGGCGGGGCGAGGCGGCCGGGCCCTGCGCGTCAGGTCCTGGCC TTGGGAGGCTGCGTCCGCGCGCCGGCGGGGCGGGGCGGCCGGGCCCTGCGCGTCAGGTCCTGGCC A G lnc-GOLGA6L22-3,lnc-GOLGA6L22-3:2 RNACentral:URS00008B995D,RNACentral:URS00008BBE5E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:22494901..22494978;chr15:22494898..22494978 26863196 MeRIP-seq:(Medium) rs1260422069 Functional Loss SNV dbSNP153 33..33 33 - - - 68431 RMVar_ID_68431 Human_SNP_ID_569976554 m1A Human chr15 - 22558073 22558071 22558073 TGGAGGACGCCCACATACCCACCCACACTCACACGTGCTCACTCTCAGTCACATGCACACTCACC TGGAGGACGCCCACATACCCACCCACACTCAC__GTGCTCACTCTCAGTCACATGCACACTCACC CGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:22558039..22558106 26863196 MeRIP-seq:(Medium) rs1193382439 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5646536,Human_RBP_ID_17206038,Human_RBP_ID_17252677 68432 RMVar_ID_68432 Human_SNP_ID_569980676 m1A Human chr15 + 22574301 22574301 22574301 AGACTACAGTAAAGGGGTGGGAGTGAGGGCACAGTCCAGGGATCGGGATCTGCAATGAGAAGGTG AGACTACAGTAAAGGGGTGGGAGTGAGGGCACGGTCCAGGGATCGGGATCTGCAATGAGAAGGTG A G HERC2P2 Ensembl:ENSG00000276550 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:22574251..22574373 26863196 MeRIP-seq:(Medium) rs1410841401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3945983,Human_RBP_ID_22473361,Human_RBP_ID_26778646 RMVar_hsa_circ_18195,RMVar_hsa_circ_23538,RMVar_hsa_circ_66642 68433 RMVar_ID_68433 Human_SNP_ID_570037061 m1A Human chr15 + 22786677 22786671 22786677 GGCGCGGGCGGAATGGGGACTGCAGCTGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA GGCGCGGGCGGAATGGGGACTGCAGCT______GCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA TGCGGCA T NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:22786650..22786884 26863196 MeRIP-seq:(Medium) rs1555371600 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4316702,Human_RBP_ID_9324451,Human_RBP_ID_9418534,Human_RBP_ID_17119991,Human_RBP_ID_18189536,Human_RBP_ID_18418426 68434 RMVar_ID_68434 Human_SNP_ID_570037067 m1A Human chr15 + 22786677 22786674 22786677 GGCGCGGGCGGAATGGGGACTGCAGCTGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA GGCGCGGGCGGAATGGGGACTGCAGCTGCG___GCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA GGCA G NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:22786650..22786884 26863196 MeRIP-seq:(Medium) rs769916931 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4316702,Human_RBP_ID_9324451,Human_RBP_ID_9418534,Human_RBP_ID_17119991,Human_RBP_ID_18189536,Human_RBP_ID_18418426 68435 RMVar_ID_68435 Human_SNP_ID_570037070 m1A Human chr15 + 22786677 22786677 22786677 GGCGCGGGCGGAATGGGGACTGCAGCTGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA GGCGCGGGCGGAATGGGGACTGCAGCTGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGA A G NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:22786650..22786884 26863196 MeRIP-seq:(Medium) rs749414711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4316702,Human_RBP_ID_9324451,Human_RBP_ID_9418534,Human_RBP_ID_17119991,Human_RBP_ID_18189536,Human_RBP_ID_18418426 68436 RMVar_ID_68436 Human_SNP_ID_570037111 m1A Human chr15 + 22786709 22786709 22786709 AGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGAGGGGGCGCGTAGCCCGAGCCCCGCCGCCGTGT AGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGGGGGGGGCGCGTAGCCCGAGCCCCGCCGCCGTGT A G NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:22786658..22786867;chr15:22786660..22786828 26863196 MeRIP-seq:(Medium) rs895212805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342188,Human_RBP_ID_5316036,Human_RBP_ID_8081778,Human_RBP_ID_9324451,Human_RBP_ID_9418535,Human_RBP_ID_17119991,Human_RBP_ID_18189536,Human_RBP_ID_18418323,Human_RBP_ID_27837489 68437 RMVar_ID_68437 Human_SNP_ID_570048465 m1A Human chr15 + 22824358 22824358 22824358 GATCATGGTGTTAGAATTGACTGGATAGTAACAGGTGGTCTGGTGGATAGCGGGGAGCATGGCTC GATCATGGTGTTAGAATTGACTGGATAGTAACCGGTGGTCTGGTGGATAGCGGGGAGCATGGCTC A C NIPA1 Ensembl:ENSG00000170113 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:22824308..22824392 26863196 MeRIP-seq:(Medium) rs1478439477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5141233,Human_RBP_ID_6414165,Human_RBP_ID_8798772,Human_RBP_ID_12481159 68438 RMVar_ID_68438 Human_SNP_ID_570057554 m1A Human chr15 - 22855618 22855618 22855618 TCCTTCCCATTTATCATCACGCACAGGCACATAAACACATAACTTCTTTATCTTGTTTAATGTCT TCCTTCCCATTTATCATCACGCACAGGCACATCAACACATAACTTCTTTATCTTGTTTAATGTCT T G RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:22855615..22855739 26863196 MeRIP-seq:(Medium) rs890158068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107200,RMVar_hsa_circ_170059,RMVar_hsa_circ_81960,RMVar_hsa_circ_170061 68439 RMVar_ID_68439 Human_SNP_ID_570093526 m1A Human chr15 - 22973415 22973415 22973415 CAGAGAGTAGACAGGTGATTGCCTGGGGCCAGAAAGCAGGGGAGAGAGGATCAGTGAAGAACGGG CAGAGAGTAGACAGGTGATTGCCTGGGGCCAGCAAGCAGGGGAGAGAGGATCAGTGAAGAACGGG T G CYFIP1 Ensembl:ENSG00000273749 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:22973413..22973481 26863196 MeRIP-seq:(Medium) rs1048897280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12480326 68440 RMVar_ID_68440 Human_SNP_ID_570095728 m1A Human chr15 - 22980303 22980303 22980303 AGGAAACTCCCAGGGCCCGCCCAGGACCCCCAAGCCGCCGCGGACGCAGGTGAGGAACCCCGCTC AGGAAACTCCCAGGGCCCGCCCAGGACCCCCAGGCCGCCGCGGACGCAGGTGAGGAACCCCGCTC T C CYFIP1 Ensembl:ENSG00000273749 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:22980214..22980305 26863196 MeRIP-seq:(Medium) rs927409831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342521,Human_RBP_ID_8804017,Human_RBP_ID_18418427 Human_Splice_Rec_1564919,Human_Splice_Rec_1565027,Human_Splice_Rec_1565143,Human_Splice_Rec_1565153 68441 RMVar_ID_68441 Human_SNP_ID_570101090 m1A Human chr15 - 22999378 22999378 22999378 CCACTTGCCCACAGTCCAGACAGATGGATTGTAGGTGGGTTTTCTGGAGATTAGTAGATACTGTA CCACTTGCCCACAGTCCAGACAGATGGATTGTGGGTGGGTTTTCTGGAGATTAGTAGATACTGTA T C TUBGCP5 Ensembl:ENSG00000275835 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1046866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18277771,Human_RBP_ID_18660677,Human_RBP_ID_21887630 RMVar_hsa_circ_21584 68442 RMVar_ID_68442 Human_SNP_ID_570112286 m1A Human chr15 - 23039509 23039509 23039509 GGCGCGGCACGGGCCACCGTGGAGTCGGTTGGACGCGCAGCAGGAGCGCGACGTGCGGGAGCTCG GGCGCGGCACGGGCCACCGTGGAGTCGGTTGGGCGCGCAGCAGGAGCGCGACGTGCGGGAGCTCG T C TUBGCP5 Ensembl:ENSG00000275835 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:23039458..23039549 26863196 MeRIP-seq:(Medium) rs766641480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342522,Human_RBP_ID_22934747,Human_RBP_ID_27809234 68443 RMVar_ID_68443 Human_SNP_ID_570228904 m1A Human chr15 - 23565932 23565932 23565932 GCTACAGGGAAGGGGGCCCAGCCCCTTGCCGCATGTGGCAGGGCTGAATCTGGAGCAGCAGATTC GCTACAGGGAAGGGGGCCCAGCCCCTTGCCGCTTGTGGCAGGGCTGAATCTGGAGCAGCAGATTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:23565884..23565971 26863196 MeRIP-seq:(Medium) rs1468076667 Functional Loss SNV dbSNP153 33..33 33 - - - 68444 RMVar_ID_68444 Human_SNP_ID_570229084 m1A Human chr15 + 23566256 23566256 23566256 CACATCGAGCCCCCGACTCAGGAAGTGGCGGAAGCCCCCCCGGCTGCATCCTCCCTTTCCTTGCC CACATCGAGCCCCCGACTCAGGAAGTGGCGGAGGCCCCCCCGGCTGCATCCTCCCTTTCCTTGCC A G MKRN3 Ensembl:ENSG00000179455 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:23566211..23566301 26863196 MeRIP-seq:(Medium) rs1411901694 Functional Loss SNV dbSNP153 33..33 33 - - - 68445 RMVar_ID_68445 Human_SNP_ID_570604990 m1A Human chr15 - 24909020 24909020 24909020 CAAGAAAGAAGTTAAAAAGAAGAGGTGGAACCATCCCAAAATGTCCCTTGCTCAGAAGAAGGATT CAAGAAAGAAGTTAAAAAGAAGAGGTGGAACCGTCCCAAAATGTCCCTTGCTCAGAAGAAGGATT T C RPL5P1 Ensembl:ENSG00000241061 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879012126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17368032 68446 RMVar_ID_68446 Human_SNP_ID_570605056 m1A Human chr15 - 24909287 24909287 24909287 TGGAGGCTTGTCTATCCCTCACAGTACCAAACAATTCCCTGGTTATGGTTCTGAAAGCAAGGAAT TGGAGGCTTGTCTATCCCTCACAGTACCAAACGATTCCCTGGTTATGGTTCTGAAAGCAAGGAAT T C RPL5P1 Ensembl:ENSG00000241061 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8023367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4344032,Human_RBP_ID_22927795,Human_RBP_ID_26433067 Human_miRNA_ID_1843121 GWAS_ID_8225,GWAS_ID_8226 68447 RMVar_ID_68447 Human_SNP_ID_570621314 m1A Human chr15 + 24967883 24967883 24967883 GGTACCTAGTTTTCTTTCATATGGTTTCCTATAAAGACAAATGTATTTTTATCATTTATATATAT GGTACCTAGTTTTCTTTCATATGGTTTCCTATTAAGACAAATGTATTTTTATCATTTATATATAT A T SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:24967880..24967965 26863196 MeRIP-seq:(Medium) rs759767759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11327,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,RMVar_hsa_circ_41388,RMVar_hsa_circ_123391,RMVar_hsa_circ_170093,RMVar_hsa_circ_170096,RMVar_hsa_circ_23619,RMVar_hsa_circ_343772,RMVar_hsa_circ_98409,RMVar_hsa_circ_170097,RMVar_hsa_circ_357218,RMVar_hsa_circ_170098,RMVar_hsa_circ_351391,RMVar_hsa_circ_273335,RMVar_hsa_circ_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_170101,RMVar_hsa_circ_170099,RMVar_hsa_circ_330240 68448 RMVar_ID_68448 Human_SNP_ID_570624060 m1A Human chr15 - 24977912 24977912 24977912 TTCGTCTTCGTGTTCACCAATCCCTTACCTGGAGGTGGGGTTGCTCTGCCGACGGGTGGGGGCGG TTCGTCTTCGTGTTCACCAATCCCTTACCTGGGGGTGGGGTTGCTCTGCCGACGGGTGGGGGCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:24977835..24977962 26863196 MeRIP-seq:(Medium) rs1302728297 Functional Loss SNV dbSNP153 33..33 33 - - - 68449 RMVar_ID_68449 Human_SNP_ID_570624061 m1A Human chr15 - 24977912 24977912 24977912 TTCGTCTTCGTGTTCACCAATCCCTTACCTGGAGGTGGGGTTGCTCTGCCGACGGGTGGGGGCGG TTCGTCTTCGTGTTCACCAATCCCTTACCTGGCGGTGGGGTTGCTCTGCCGACGGGTGGGGGCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:24977835..24977962 26863196 MeRIP-seq:(Medium) rs1302728297 Functional Loss SNV dbSNP153 33..33 33 - - - 68450 RMVar_ID_68450 Human_SNP_ID_570650404 m1A Human chr15 + 25071873 25071873 25071873 TGCAGGCATTGTTGTGGGTGGGAATGCGGTCAAGCTGACTGCACGATGGGACATTGCCTCTGAGG TGCAGGCATTGTTGTGGGTGGGAATGCGGTCAGGCTGACTGCACGATGGGACATTGCCTCTGAGG A G SNHG14 Ensembl:ENSG00000224078 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:25071745..25071874 26863196 MeRIP-seq:(Medium) rs1415907451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814418,Human_RBP_ID_17119485 RMVar_hsa_circ_2016,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_36518,RMVar_hsa_circ_12212,RMVar_hsa_circ_669,RMVar_hsa_circ_40916,RMVar_hsa_circ_360408,RMVar_hsa_circ_366017,RMVar_hsa_circ_55391,RMVar_hsa_circ_28895,RMVar_hsa_circ_170143,RMVar_hsa_circ_13407,RMVar_hsa_circ_45622,RMVar_hsa_circ_12039,RMVar_hsa_circ_68809,RMVar_hsa_circ_21064,RMVar_hsa_circ_112246,RMVar_hsa_circ_102574,RMVar_hsa_circ_32357,RMVar_hsa_circ_101435,RMVar_hsa_circ_170152,RMVar_hsa_circ_170154,RMVar_hsa_circ_85418,RMVar_hsa_circ_170153,RMVar_hsa_circ_124874,RMVar_hsa_circ_170155,RMVar_hsa_circ_84095,RMVar_hsa_circ_93845,RMVar_hsa_circ_170156,RMVar_hsa_circ_127042,RMVar_hsa_circ_119790,RMVar_hsa_circ_121332,RMVar_hsa_circ_116081,RMVar_hsa_circ_99252,RMVar_hsa_circ_104240,RMVar_hsa_circ_105279,RMVar_hsa_circ_103126,RMVar_hsa_circ_80505,RMVar_hsa_circ_86144,RMVar_hsa_circ_76514,RMVar_hsa_circ_170157,RMVar_hsa_circ_170161,RMVar_hsa_circ_170165,RMVar_hsa_circ_170167,RMVar_hsa_circ_170168,RMVar_hsa_circ_170169,RMVar_hsa_circ_170166,RMVar_hsa_circ_170163,RMVar_hsa_circ_170164,RMVar_hsa_circ_170162,RMVar_hsa_circ_170159,RMVar_hsa_circ_170160,RMVar_hsa_circ_170158,RMVar_hsa_circ_61955,RMVar_hsa_circ_64265,RMVar_hsa_circ_55983 68451 RMVar_ID_68451 Human_SNP_ID_570653702 m1A Human chr15 - 25082535 25082535 25082535 CGGGTGTGCTTGAGAAAGGCAGGCAAACACATAGGTCACAAGGGCCATGCCATTCAACCCCCTGT CGGGTGTGCTTGAGAAAGGCAGGCAAACACATCGGTCACAAGGGCCATGCCATTCAACCCCCTGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:25082529..25082618 26863196 MeRIP-seq:(Medium) rs1425177639 Functional Loss SNV dbSNP153 33..33 33 - - - 68452 RMVar_ID_68452 Human_SNP_ID_570662997 m1A Human chr15 - 25115545 25115545 25115545 AGAGAGAGAGAGAGAGAGAGAGAGAGACACCCAGGGGCCAATGCCCTTATTGGGTCAAGGGTACT AGAGAGAGAGAGAGAGAGAGAGAGAGACACCCTGGGGCCAATGCCCTTATTGGGTCAAGGGTACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:25115497..25115596 26863196 MeRIP-seq:(Medium) rs919292538 Functional Loss SNV dbSNP153 33..33 33 - - - 68453 RMVar_ID_68453 Human_SNP_ID_570753859 m1A Human chr15 - 25438587 25438561 25438588 GCGGGTCCCGCATGAGCCCCGGCGGTGGCGGCAGCGAAAGAGAACGAGGCGGTGGCGGGCGGAGG GCGGGTCCCGCATGAGCCCCGGCGGTGGCGG___________________________GCGGAGG CCCGCCACCGCCTCGTTCTCTTTCGCTG C UBE3A Ensembl:ENSG00000114062 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:25438536..25438608;chr15:25438539..25438632 26863196 MeRIP-seq:(Medium) rs1453757060 Functional Loss DEL dbSNP153 32..58 33 - - - Human_RBP_ID_4342973,Human_RBP_ID_8803687,Human_RBP_ID_18458158,Human_RBP_ID_22047792,Human_RBP_ID_25131643 Human_Splice_Rec_1572249,Human_Splice_Rec_1572275,Human_Splice_Rec_1572301,Human_Splice_Rec_1572333,Human_Splice_Rec_1572351,Human_Splice_Rec_1572379,Human_Splice_Rec_1572403,Human_Splice_Rec_1572429,Human_Splice_Rec_1572449,Human_Splice_Rec_1572475,Human_Splice_Rec_1572503,Human_Splice_Rec_1572545,Human_Splice_Rec_1572573,Human_Splice_Rec_1572613,Human_Splice_Rec_1572619,Human_Splice_Rec_1572635 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238,RMVar_hsa_circ_170243,RMVar_hsa_circ_78513 68454 RMVar_ID_68454 Human_SNP_ID_570753866 m1A Human chr15 - 25438587 25438587 25438587 GCGGGTCCCGCATGAGCCCCGGCGGTGGCGGCAGCGAAAGAGAACGAGGCGGTGGCGGGCGGAGG GCGGGTCCCGCATGAGCCCCGGCGGTGGCGGCGGCGAAAGAGAACGAGGCGGTGGCGGGCGGAGG T C UBE3A Ensembl:ENSG00000114062 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:25438536..25438608;chr15:25438539..25438632 26863196 MeRIP-seq:(Medium) rs1001161353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342973,Human_RBP_ID_8803687,Human_RBP_ID_18458158,Human_RBP_ID_22047792,Human_RBP_ID_25131643 Human_Splice_Rec_1572249,Human_Splice_Rec_1572275,Human_Splice_Rec_1572301,Human_Splice_Rec_1572333,Human_Splice_Rec_1572351,Human_Splice_Rec_1572379,Human_Splice_Rec_1572403,Human_Splice_Rec_1572429,Human_Splice_Rec_1572449,Human_Splice_Rec_1572475,Human_Splice_Rec_1572503,Human_Splice_Rec_1572545,Human_Splice_Rec_1572573,Human_Splice_Rec_1572613,Human_Splice_Rec_1572619,Human_Splice_Rec_1572635 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238,RMVar_hsa_circ_170243,RMVar_hsa_circ_78513 68455 RMVar_ID_68455 Human_SNP_ID_571080401 m1A Human chr15 + 26716822 26716809 26716823 CAGCTCTGAGGACCTCCACCCAACCACAGCCCAGCTCTGAGGACCTCCACCCAACCACAGCCCAG CAGCTCTGAGGACCTCCACC______________CTCTGAGGACCTCCACCCAACCACAGCCCAG CCAACCACAGCCCAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:26716749..26716900 26863196 MeRIP-seq:(Medium) rs1566816838 Functional Loss DEL dbSNP153 21..34 33 - - - 68456 RMVar_ID_68456 Human_SNP_ID_571427002 m1A Human chr15 + 28117471 28117471 28117471 CACCACCACCACGTCCACAGCTGCGGCCCGGCAGCACCACCCTGGCACGGACCATCCTCACACCC CACCACCACCACGTCCACAGCTGCGGCCCGGCGGCACCACCCTGGCACGGACCATCCTCACACCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:28117466..28117592 26863196 MeRIP-seq:(Medium) rs1409179920 Functional Loss SNV dbSNP153 33..33 33 - - - 68457 RMVar_ID_68457 Human_SNP_ID_571428671 m1A Human chr15 - 28124195 28124195 28124195 TGGAGTACAATCACCTGCAGGAGATCCCCATCATTGCGCTGAGGAACCGTCTGCTGCTGCTGCAC TGGAGTACAATCACCTGCAGGAGATCCCCATCGTTGCGCTGAGGAACCGTCTGCTGCTGCTGCAC T C HERC2 Ensembl:ENSG00000128731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:28124145..28124275 26863196 MeRIP-seq:(Medium) rs749216967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18189542 Human_Splice_Rec_1573974,Human_Splice_Rec_1574050 Human_miRNA_ID_2999297 RMVar_hsa_circ_7037,RMVar_hsa_circ_87685,RMVar_hsa_circ_94513,RMVar_hsa_circ_109691,RMVar_hsa_circ_170285,RMVar_hsa_circ_102114,RMVar_hsa_circ_170286,RMVar_hsa_circ_170287,RMVar_hsa_circ_106541,RMVar_hsa_circ_170288,RMVar_hsa_circ_170289,RMVar_hsa_circ_170290,RMVar_hsa_circ_107785,RMVar_hsa_circ_267982,RMVar_hsa_circ_47303,RMVar_hsa_circ_170291 68458 RMVar_ID_68458 Human_SNP_ID_571453032 m1A Human chr15 - 28217161 28217152 28217162 ATGAGACACCCAGTGTAAGTGTAAGTCAGTGTAAGTCAGTGAGGGTTGGTGAGTGTGAGGAAGTA ATGAGACACCCAGTGTAAGTGTAAGTCAGTG__________AGGGTTGGTGAGTGTGAGGAAGTA TCACTGACTTA T HERC2 Ensembl:ENSG00000128731 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:28217064..28217400 26863196 MeRIP-seq:(Medium) rs1432193328 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_3488776,Human_RBP_ID_5141359,Human_RBP_ID_5236307,Human_RBP_ID_5287390,Human_RBP_ID_24368349 RMVar_hsa_circ_94513,RMVar_hsa_circ_170285,RMVar_hsa_circ_102114,RMVar_hsa_circ_106541,RMVar_hsa_circ_170288,RMVar_hsa_circ_170289,RMVar_hsa_circ_81630,RMVar_hsa_circ_170297,RMVar_hsa_circ_89074,RMVar_hsa_circ_170299,RMVar_hsa_circ_109327,RMVar_hsa_circ_170301,RMVar_hsa_circ_87491,RMVar_hsa_circ_170307,RMVar_hsa_circ_94296,RMVar_hsa_circ_170309,RMVar_hsa_circ_116251,RMVar_hsa_circ_170312,RMVar_hsa_circ_121229,RMVar_hsa_circ_170316,RMVar_hsa_circ_76113,RMVar_hsa_circ_114057,RMVar_hsa_circ_113452,RMVar_hsa_circ_170320,RMVar_hsa_circ_170321,RMVar_hsa_circ_103161,RMVar_hsa_circ_119194,RMVar_hsa_circ_170323,RMVar_hsa_circ_170324,RMVar_hsa_circ_95740,RMVar_hsa_circ_102750,RMVar_hsa_circ_109209,RMVar_hsa_circ_267700,RMVar_hsa_circ_170325,RMVar_hsa_circ_265175,RMVar_hsa_circ_108511,RMVar_hsa_circ_372376,RMVar_hsa_circ_170326,RMVar_hsa_circ_170327,RMVar_hsa_circ_118644,RMVar_hsa_circ_170328,RMVar_hsa_circ_93946,RMVar_hsa_circ_99696,RMVar_hsa_circ_77900,RMVar_hsa_circ_124506,RMVar_hsa_circ_170330,RMVar_hsa_circ_170332,RMVar_hsa_circ_170333,RMVar_hsa_circ_170334,RMVar_hsa_circ_170331,RMVar_hsa_circ_170329,RMVar_hsa_circ_170335 68459 RMVar_ID_68459 Human_SNP_ID_571468487 m1A Human chr15 + 28274456 28274456 28274456 CACTGCAGAGGTCCGCATCCTCGCCTGGGCGCACACACGCGTCAGAGGAGCCCCCCCACTCCCCT CACTGCAGAGGTCCGCATCCTCGCCTGGGCGCGCACACGCGTCAGAGGAGCCCCCCCACTCCCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:28274450..28274598 26863196 MeRIP-seq:(Medium) rs1324072419 Functional Loss SNV dbSNP153 33..33 33 - - - 68460 RMVar_ID_68460 Human_SNP_ID_571544594 m1A Human chr15 - 28652760 28652760 28652760 GAATGTAGTCACCTGCCCACTCACATGCTCTCATGGACACACACCCACACAACCACATGCTACAA GAATGTAGTCACCTGCCCACTCACATGCTCTCGTGGACACACACCCACACAACCACATGCTACAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:28652586..28652801 26863196 MeRIP-seq:(Medium) rs1433929131 Functional Loss SNV dbSNP153 33..33 33 - - - 68461 RMVar_ID_68461 Human_SNP_ID_571544682 m1A Human chr15 + 28652969 28652969 28652969 TGAGTGTGAGGAAGTATGAGTGGGTGGCAGGCACAAGTGTAAGTGTGCGATTGAGTGCGAGCATT TGAGTGTGAGGAAGTATGAGTGGGTGGCAGGCGCAAGTGTAAGTGTGCGATTGAGTGCGAGCATT A G HERC2P9 Ensembl:ENSG00000206149 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:28652945..28653011 26863196 MeRIP-seq:(Medium) rs560908021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490658,Human_RBP_ID_5287395,Human_RBP_ID_5646158,Human_RBP_ID_17252691,Human_RBP_ID_17673217 RMVar_hsa_circ_10378 68462 RMVar_ID_68462 Human_SNP_ID_571649959 m1A Human chr15 - 29054284 29054284 29054284 CGAGTCCGTCCACTCCTCCACCGCCTCCTGGCACTCATCAGTGTCCACAGGGTGTGCACTGTGGG CGAGTCCGTCCACTCCTCCACCGCCTCCTGGCGCTCATCAGTGTCCACAGGGTGTGCACTGTGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:29054235..29054485 32194978 MeRIP-seq:(Medium) rs749183539 Functional Loss SNV dbSNP153 33..33 33 - - - 68463 RMVar_ID_68463 Human_SNP_ID_571661911 m1A Human chr15 - 29101711 29101711 29101711 TCTTGCCTTCCTGGGCCCCGGGCGTGGTCTCGATGCAGTCCTGAGAGGCTGACCGGGGCATGCGG TCTTGCCTTCCTGGGCCCCGGGCGTGGTCTCGGTGCAGTCCTGAGAGGCTGACCGGGGCATGCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:29101662..29101812 32194978 MeRIP-seq:(Medium) rs771392666 Functional Loss SNV dbSNP153 33..33 33 - - - 68464 RMVar_ID_68464 Human_SNP_ID_571662974 m1A Human chr15 + 29105476 29105476 29105476 CAATGGCATCAACCCCGAAGACTTGAGCCAGAAGGAATACAGCGACATCATCAACACCCAGGAGA CAATGGCATCAACCCCGAAGACTTGAGCCAGAGGGAATACAGCGACATCATCAACACCCAGGAGA A G APBA2 Ensembl:ENSG00000034053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:29105426..29105526;chr15:29105426..29108472 32194978 MeRIP-seq:(Medium) rs1384440989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27810032 Human_Splice_Rec_1574880,Human_Splice_Rec_1574881,Human_Splice_Rec_1574910,Human_Splice_Rec_1574911,Human_Splice_Rec_1574938,Human_Splice_Rec_1574939,Human_Splice_Rec_1574964,Human_Splice_Rec_1574965,Human_Splice_Rec_1575002,Human_Splice_Rec_1575003,Human_Splice_Rec_1575026,Human_Splice_Rec_1575027 68465 RMVar_ID_68465 Human_SNP_ID_571667035 m1A Human chr15 + 29117617 29117617 29117617 AAACAGCTGCCTCTGCCACTGACTGCAGGGACACGGGCAGCCTGGCTCCCAGGACACGACTTGTA AAACAGCTGCCTCTGCCACTGACTGCAGGGACGCGGGCAGCCTGGCTCCCAGGACACGACTTGTA A G APBA2 Ensembl:ENSG00000034053 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:29117567..29117668 32194978 MeRIP-seq:(Medium) rs1464581945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18661004,Human_RBP_ID_21887641,Human_RBP_ID_23647576 68466 RMVar_ID_68466 Human_SNP_ID_571706562 m1A Human chr15 + 29268782 29268782 29268782 GTCTCAGACCCTTGTCCCGGGGGTCCCTCTGAATCCACCTTTCAAGAGGATGGAGCTGGGCCACT GTCTCAGACCCTTGTCCCGGGGGTCCCTCTGACTCCACCTTTCAAGAGGATGGAGCTGGGCCACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:29268731..29268941 26863196 MeRIP-seq:(Medium) rs201961141 Functional Loss SNV dbSNP153 33..33 33 - - - 68467 RMVar_ID_68467 Human_SNP_ID_571707007 m1A Human chr15 - 29269647 29269647 29269647 CCGCTCTGGCGGCCAGGCCGAGAGGGACAGAGACTGGAGCCATAGCGGAAACCCCGGGGCTTCGC CCGCTCTGGCGGCCAGGCCGAGAGGGACAGAGGCTGGAGCCATAGCGGAAACCCCGGGGCTTCGC T C FAM189A1,NSMCE3 Ensembl:ENSG00000104059,Ensembl:ENSG00000185115 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:29269597..29269800 26863196 MeRIP-seq:(Medium) rs773214385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1000238 68468 RMVar_ID_68468 Human_SNP_ID_571707079 m1A Human chr15 + 29269740 29269740 29269740 CTCCGGCGGCAGGTGCCGGCGCACACTCCGGTAGGCAAGCAGCCGCGGCGGGGATTGCGGGTCGG CTCCGGCGGCAGGTGCCGGCGCACACTCCGGTGGGCAAGCAGCCGCGGCGGGGATTGCGGGTCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:29269661..29269765 26863410 MeRIP-seq:(Medium) rs556570084 Functional Loss SNV dbSNP153 33..33 33 - - - 68469 RMVar_ID_68469 Human_SNP_ID_571812467 m1A Human chr15 + 29675258 29675258 29675258 TCTCCCCAGGCCCCCGCTTTGGCCACCCAGGCACTTTCCGCCCTGAGCGTGGCAGCTGCTGCCGG TCTCCCCAGGCCCCCGCTTTGGCCACCCAGGCTCTTTCCGCCCTGAGCGTGGCAGCTGCTGCCGG A T AC022613.1 Ensembl:ENSG00000256802 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:29675191..29675304 32194978 MeRIP-seq:(Medium) rs1386333023 Functional Loss SNV dbSNP153 33..33 33 - - - 68470 RMVar_ID_68470 Human_SNP_ID_571852190 m1A Human chr15 - 29821974 29821974 29821974 CCAAGGTGAGCGCCTCCGCGGCCGCCAGGGCCAGACCGGGCCGACCGTCGCCGCCCGCCCACCGG CCAAGGTGAGCGCCTCCGCGGCCGCCAGGGCCGGACCGGGCCGACCGTCGCCGCCCGCCCACCGG T C TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:29821964..29822111 26863196 MeRIP-seq:(Medium) rs531384390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19067061,Human_RBP_ID_26778847 68471 RMVar_ID_68471 Human_SNP_ID_571852375 m1A Human chr15 - 29822371 29822371 29822371 CCCGGGAAGTTACGTGGCGAAGCCGGCTTCCGAGGAGACGCCGGGAGGCCACGGGTGCTGCTGAC CCCGGGAAGTTACGTGGCGAAGCCGGCTTCCGTGGAGACGCCGGGAGGCCACGGGTGCTGCTGAC T A TJP1 Ensembl:ENSG00000104067 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:29822170..29822400 26863196 MeRIP-seq:(Medium) rs1005841303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342198,Human_RBP_ID_8804032,Human_RBP_ID_9283570,Human_RBP_ID_22934550,Human_RBP_ID_24558510 68472 RMVar_ID_68472 Human_SNP_ID_571852376 m1A Human chr15 - 29822371 29822371 29822371 CCCGGGAAGTTACGTGGCGAAGCCGGCTTCCGAGGAGACGCCGGGAGGCCACGGGTGCTGCTGAC CCCGGGAAGTTACGTGGCGAAGCCGGCTTCCGGGGAGACGCCGGGAGGCCACGGGTGCTGCTGAC T C TJP1 Ensembl:ENSG00000104067 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:29822170..29822400 26863196 MeRIP-seq:(Medium) rs1005841303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342198,Human_RBP_ID_8804032,Human_RBP_ID_9283570,Human_RBP_ID_22934550,Human_RBP_ID_24558510 68473 RMVar_ID_68473 Human_SNP_ID_571852421 m1A Human chr15 - 29822436 29822436 29822436 GTGGCCGCTGAGTTGCCGGCGCCGGCTGAGCCAGCGGACGCCGCGTTCCTTGGCGGCCGCCGGTT GTGGCCGCTGAGTTGCCGGCGCCGGCTGAGCCGGCGGACGCCGCGTTCCTTGGCGGCCGCCGGTT T C TJP1 Ensembl:ENSG00000104067 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:29821961..29822500 26863196 MeRIP-seq:(Medium) rs1080529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232540,Human_RBP_ID_4342199,Human_RBP_ID_8804032,Human_RBP_ID_22047371 68474 RMVar_ID_68474 Human_SNP_ID_571882412 m1A Human chr15 - 29949625 29949598 29949625 GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGGTGGTTG GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGG___________________________TGGTTG ACCACCTCCACCTTCACCACCACCACCT A TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:29949524..29949650 26863196 MeRIP-seq:(Medium) rs1567225551 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68475 RMVar_ID_68475 Human_SNP_ID_571882449 m1A Human chr15 - 29949625 29949625 29949625 GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGGTGGTTG GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGTGGTGGTGGTGGTGAAGGTGGAGGTGGTGGTTG T A TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:29949524..29949650 26863196 MeRIP-seq:(Medium) rs865914644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68476 RMVar_ID_68476 Human_SNP_ID_571882450 m1A Human chr15 - 29949625 29949625 29949625 GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGGTGGTTG GGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGGGGTGGTGGTGGTGAAGGTGGAGGTGGTGGTTG T C TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:29949524..29949650 26863196 MeRIP-seq:(Medium) rs865914644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68477 RMVar_ID_68477 Human_SNP_ID_571882457 m1A Human chr15 - 29949631 29949631 29949631 GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG T A TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:29949576..29949672 26863196 MeRIP-seq:(Medium) rs1290228988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68478 RMVar_ID_68478 Human_SNP_ID_571882458 m1A Human chr15 - 29949631 29949631 29949631 GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGGGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG T C TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:29949576..29949672 26863196 MeRIP-seq:(Medium) rs1290228988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68479 RMVar_ID_68479 Human_SNP_ID_571882459 m1A Human chr15 - 29949631 29949631 29949631 GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGAGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG GGAGGTGGAGGTGGTGGTGGTGGAGGTGGTGGCGGTGGAGGTGGTGGTGGTGAAGGTGGAGGTGG T G TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:29949576..29949672 26863196 MeRIP-seq:(Medium) rs1290228988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260863,Human_RBP_ID_814268,Human_RBP_ID_3489047,Human_RBP_ID_8182527,Human_RBP_ID_8230693 RMVar_hsa_circ_170428,RMVar_hsa_circ_170430 68480 RMVar_ID_68480 Human_SNP_ID_571887794 m1A Human chr15 - 29968970 29968939 29968971 AGCTGCGGGCCACGCACGGCGGCGGCGGCGGGAGCGGCCGGGCACGCACGGCGACGGCGGCGGCG AGCTGCGGGCCACGCACGGCGGCGGCGGCGG________________________________CG GCCGCCGCCGTCGCCGTGCGTGCCCGGCCGCTC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:29968895..29968993 26863410 MeRIP-seq:(Medium) rs1366761514 Functional Loss DEL dbSNP153 32..63 33 - - - 68481 RMVar_ID_68481 Human_SNP_ID_267939214 m1A Human chr6 - 15245650 15245649 15245650 TCACCCCCTTTCCCCTGCCTGCCGCTCACCCCACGGCCGCCCCACGCCAGCCCCCGCCACTGCCT TCACCCCCTTTCCCCTGCCTGCCGCTCACCCC_CGGCCGCCCCACGCCAGCCCCCGCCACTGCCT GT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:15245613..15245713 26863196 MeRIP-seq:(Medium) rs1329774452 Functional Loss DEL dbSNP153 33..33 33 - - - 68482 RMVar_ID_68482 Human_SNP_ID_267940420 m1A Human chr6 - 15248854 15248854 15248854 GCCCGGCTCTGCGGCAGCCCCCGCCCCCGCCCAGCTCCCTCCTCCCCCCGCCGCCCCGCCGCGCC GCCCGGCTCTGCGGCAGCCCCCGCCCCCGCCCCGCTCCCTCCTCCCCCCGCCGCCCCGCCGCGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:15248847..15248972 26863196 MeRIP-seq:(Medium) rs1018070773 Functional Loss SNV dbSNP153 33..33 33 - - - 68483 RMVar_ID_68483 Human_SNP_ID_268012261 m1A Human chr6 + 15496568 15496568 15496568 GCGGAACTCCAAGAGGAGACTGGAAGAGGCACACCAGGCGGAGAAGCCGCAGTCGCCCCCCAAGA GCGGAACTCCAAGAGGAGACTGGAAGAGGCACGCCAGGCGGAGAAGCCGCAGTCGCCCCCCAAGA A G JARID2 Ensembl:ENSG00000008083 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:15496519..15496791 26863196 MeRIP-seq:(Medium) rs868306515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214825,Human_RBP_ID_947352,Human_RBP_ID_3969523,Human_RBP_ID_5532311,Human_RBP_ID_8905102,Human_RBP_ID_9309102,Human_RBP_ID_18425809,Human_RBP_ID_22104618,Human_RBP_ID_22728123,Human_RBP_ID_24548339,Human_RBP_ID_26353415,Human_RBP_ID_26771870,Human_RBP_ID_27574244,Human_RBP_ID_27827311 RMVar_hsa_circ_50801,RMVar_hsa_circ_61103,RMVar_hsa_circ_19729,RMVar_hsa_circ_89803,RMVar_hsa_circ_266036,RMVar_hsa_circ_237259,RMVar_hsa_circ_23857,RMVar_hsa_circ_66832,RMVar_hsa_circ_337833,RMVar_hsa_circ_38132,RMVar_hsa_circ_322175,RMVar_hsa_circ_3965 68484 RMVar_ID_68484 Human_SNP_ID_268020293 m1A Human chr6 + 15520888 15520886 15520888 AGGAGACGGGAGCGAGTGGGCTCTCCACCAGCACATCACTATGCATCTGTTCCAGGAAAGAAGAA AGGAGACGGGAGCGAGTGGGCTCTCCACCAG__CATCACTATGCATCTGTTCCAGGAAAGAAGAA GCA G JARID2 Ensembl:ENSG00000008083 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:15520838..15520936 26863196 MeRIP-seq:(Medium) rs1283833564 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17418666,Human_RBP_ID_18068011 Human_miRNA_ID_626254,Human_miRNA_ID_1333147 68485 RMVar_ID_68485 Human_SNP_ID_268021303 m1A Human chr6 + 15523200 15523200 15523200 GGATTTGGAACCTGGAGGGTAATCTCATTCTGACAGGTACTGGATTCAGGCCCTGCAAAATAACG GGATTTGGAACCTGGAGGGTAATCTCATTCTGGCAGGTACTGGATTCAGGCCCTGCAAAATAACG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:15522849..15523587 32194978 MeRIP-seq:(Medium) rs762788672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18857095 68486 RMVar_ID_68486 Human_SNP_ID_268042939 m1A Human chr6 - 15615320 15615320 15615320 CTGGAAGACTTATGTGGGCAGTGTGAATTAGAAAGATGCAAACATATGCAGTCCCAGCAACTGGA CTGGAAGACTTATGTGGGCAGTGTGAATTAGAGAGATGCAAACATATGCAGTCCCAGCAACTGGA T C DTNBP1 Ensembl:ENSG00000047579 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:15615216..15615321 26863196 MeRIP-seq:(Medium) rs1380323483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968565,Human_RBP_ID_8635010,Human_RBP_ID_15701164,Human_RBP_ID_24142777,Human_RBP_ID_26353417 Human_Splice_Rec_739902,Human_Splice_Rec_739903,Human_Splice_Rec_739918,Human_Splice_Rec_739919,Human_Splice_Rec_739930,Human_Splice_Rec_739931,Human_Splice_Rec_739944,Human_Splice_Rec_739945,Human_Splice_Rec_739958,Human_Splice_Rec_739959,Human_Splice_Rec_739978,Human_Splice_Rec_739979,Human_Splice_Rec_740000,Human_Splice_Rec_740001,Human_Splice_Rec_740016,Human_Splice_Rec_740017,Human_Splice_Rec_740026,Human_Splice_Rec_740027 RMVar_hsa_circ_72232,RMVar_hsa_circ_110584,RMVar_hsa_circ_237264,RMVar_hsa_circ_237265,RMVar_hsa_circ_237267,RMVar_hsa_circ_283236,RMVar_hsa_circ_325264,RMVar_hsa_circ_280735,RMVar_hsa_circ_237266 68487 RMVar_ID_68487 Human_SNP_ID_268042941 m1A Human chr6 - 15615323 15615323 15615323 CATCTGGAAGACTTATGTGGGCAGTGTGAATTAGAAAGATGCAAACATATGCAGTCCCAGCAACT CATCTGGAAGACTTATGTGGGCAGTGTGAATTGGAAAGATGCAAACATATGCAGTCCCAGCAACT T C DTNBP1 Ensembl:ENSG00000047579 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:15615251..15615360;chr6:15615225..15615349 26863196 MeRIP-seq:(Medium) rs771203317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968565,Human_RBP_ID_8635010,Human_RBP_ID_15701164,Human_RBP_ID_22306991,Human_RBP_ID_24142777,Human_RBP_ID_26353417 Human_Splice_Rec_739902,Human_Splice_Rec_739903,Human_Splice_Rec_739918,Human_Splice_Rec_739919,Human_Splice_Rec_739930,Human_Splice_Rec_739931,Human_Splice_Rec_739944,Human_Splice_Rec_739945,Human_Splice_Rec_739958,Human_Splice_Rec_739959,Human_Splice_Rec_739978,Human_Splice_Rec_739979,Human_Splice_Rec_740000,Human_Splice_Rec_740001,Human_Splice_Rec_740016,Human_Splice_Rec_740017,Human_Splice_Rec_740026,Human_Splice_Rec_740027 RMVar_hsa_circ_72232,RMVar_hsa_circ_110584,RMVar_hsa_circ_237264,RMVar_hsa_circ_237265,RMVar_hsa_circ_237267,RMVar_hsa_circ_283236,RMVar_hsa_circ_325264,RMVar_hsa_circ_280735,RMVar_hsa_circ_237266 68488 RMVar_ID_68488 Human_SNP_ID_268045665 m1A Human chr6 + 15627467 15627467 15627467 TCCCAGTGCGCAGAAAGCATGACCACCTCGCTATCCACCAGCTGCAGCACACAAGAAGGGGGGTA TCCCAGTGCGCAGAAAGCATGACCACCTCGCTGTCCACCAGCTGCAGCACACAAGAAGGGGGGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:15627417..15627523 26863196 MeRIP-seq:(Medium) rs1238265151 Functional Loss SNV dbSNP153 33..33 33 - - - 68489 RMVar_ID_68489 Human_SNP_ID_268053808 m1A Human chr6 - 15662902 15662902 15662902 ACCCAGGGGGCGACAGAGGCAGCAGCAGCCCGAGGCCTGAGGAGAGGAGACCGGCGGCGGCGGCA ACCCAGGGGGCGACAGAGGCAGCAGCAGCCCGCGGCCTGAGGAGAGGAGACCGGCGGCGGCGGCA T G DTNBP1 Ensembl:ENSG00000047579 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:15662851..15662991 26863196 MeRIP-seq:(Medium) rs776618832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968567,Human_RBP_ID_4903699,Human_RBP_ID_5122601,Human_RBP_ID_5327052,Human_RBP_ID_9309509,Human_RBP_ID_9336464,Human_RBP_ID_9350388,Human_RBP_ID_9437739,Human_RBP_ID_18425356,Human_RBP_ID_22105605,Human_RBP_ID_26353421,Human_RBP_ID_26771714,Human_RBP_ID_26792565,Human_RBP_ID_27842369 Human_Splice_Rec_739893,Human_Splice_Rec_739909,Human_Splice_Rec_739925,Human_Splice_Rec_739937,Human_Splice_Rec_739951,Human_Splice_Rec_739967,Human_Splice_Rec_739991,Human_Splice_Rec_740005,Human_Splice_Rec_740021 68490 RMVar_ID_68490 Human_SNP_ID_268053842 m1A Human chr6 - 15662956 15662956 15662956 GCCGGTAGTGGGAGTGCGGGGCGCGCGGTGACAGCGCGGGGTTGGCGGCGTGGGACCCAGGGGGC GCCGGTAGTGGGAGTGCGGGGCGCGCGGTGACGGCGCGGGGTTGGCGGCGTGGGACCCAGGGGGC T C DTNBP1 Ensembl:ENSG00000047579 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:15662801..15663055;chr6:15662785..15663075 26863196 MeRIP-seq:(Medium) rs758021979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81258,Human_RBP_ID_840809,Human_RBP_ID_3968567,Human_RBP_ID_4870333,Human_RBP_ID_5122601,Human_RBP_ID_5327052,Human_RBP_ID_9309509,Human_RBP_ID_9335960,Human_RBP_ID_9437353,Human_RBP_ID_18425356,Human_RBP_ID_24142807,Human_RBP_ID_26353421,Human_RBP_ID_26771714,Human_RBP_ID_26792565,Human_RBP_ID_27842369 68491 RMVar_ID_68491 Human_SNP_ID_268166736 m1A Human chr6 - 16129146 16129146 16129146 GCGGCCGCCACTCGCGTCCCCGCCACCCCCTCACCCGCTGCCCGCCAGCTGCCCCTGTCCTCCGC GCGGCCGCCACTCGCGTCCCCGCCACCCCCTCCCCCGCTGCCCGCCAGCTGCCCCTGTCCTCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:16129076..16129437;chr6:16129076..16130570 26863196 MeRIP-seq:(Medium) rs1389206121 Functional Loss SNV dbSNP153 33..33 33 - - - 68492 RMVar_ID_68492 Human_SNP_ID_268199042 m1A Human chr6 + 16238694 16238694 16238694 TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCATGCCCCGCATAGATGCGGACCTCAAGCTCGAC TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCCTGCCCCGCATAGATGCGGACCTCAAGCTCGAC A C GMPR Ensembl:ENSG00000137198 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:16238605..16238748 26863410 MeRIP-seq:(Medium) rs534125759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4872567,Human_RBP_ID_9335963 Human_Splice_Rec_740053 68493 RMVar_ID_68493 Human_SNP_ID_268199043 m1A Human chr6 + 16238694 16238694 16238694 TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCATGCCCCGCATAGATGCGGACCTCAAGCTCGAC TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCGTGCCCCGCATAGATGCGGACCTCAAGCTCGAC A G GMPR Ensembl:ENSG00000137198 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:16238605..16238748 26863410 MeRIP-seq:(Medium) rs534125759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4872567,Human_RBP_ID_9335963 Human_Splice_Rec_740053 68494 RMVar_ID_68494 Human_SNP_ID_268199044 m1A Human chr6 + 16238694 16238694 16238694 TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCATGCCCCGCATAGATGCGGACCTCAAGCTCGAC TCGCCGCCGCCGCAGCCAGGAGCCGCTGCACCTTGCCCCGCATAGATGCGGACCTCAAGCTCGAC A T GMPR Ensembl:ENSG00000137198 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:16238605..16238748 26863410 MeRIP-seq:(Medium) rs534125759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4872567,Human_RBP_ID_9335963 Human_Splice_Rec_740053 68495 RMVar_ID_68495 Human_SNP_ID_268210330 m1A Human chr6 - 16278130 16278130 16278130 AGCTGTTTGTCCATCTCCCTCCTGGCTGCCCCACCTCAAGTCCCTTGCAGCCTAGCCCGAGGTTC AGCTGTTTGTCCATCTCCCTCCTGGCTGCCCCGCCTCAAGTCCCTTGCAGCCTAGCCCGAGGTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:16278084..16278185 26863196 MeRIP-seq:(Medium) rs1399315248 Functional Loss SNV dbSNP153 33..33 33 - - - 68496 RMVar_ID_68496 Human_SNP_ID_268223803 m1A Human chr6 + 16327452 16327452 16327452 GCCGGAGTCGGCGTATTGCATGACGACCTGGGAGGGGGGCCCCAGGGTGAGCGTGTGTGGGATCA GCCGGAGTCGGCGTATTGCATGACGACCTGGGTGGGGGGCCCCAGGGTGAGCGTGTGTGGGATCA A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:16327409..16327531 26863196 MeRIP-seq:(Medium) rs1561852384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237280 68497 RMVar_ID_68497 Human_SNP_ID_268228312 m1A Human chr6 - 16344108 16344108 16344108 GGAGTGGGGAGAGCCTTAAGGAGGTGACATGGAAGGAGAGACCTGAAAGATGGGTGAGGCCAGTG GGAGTGGGGAGAGCCTTAAGGAGGTGACATGGGAGGAGAGACCTGAAAGATGGGTGAGGCCAGTG T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:16344104..16344199 26863196 MeRIP-seq:(Medium) rs1387173839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279 68498 RMVar_ID_68498 Human_SNP_ID_268251448 m1A Human chr6 - 16439384 16439381 16439385 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCT____CCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GAATA G ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1561896220 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68499 RMVar_ID_68499 Human_SNP_ID_268251450 m1A Human chr6 + 16439383 16439382 16439384 GGGGGGGGGGCGGGGCCGGGGGCGGGGCGGGAATAAGGGTTGGGGTGGGGTGGGGATGCTGACAT GGGGGGGGGGCGGGGCCGGGGGCGGGGCGGGA__AAGGGTTGGGGTGGGGTGGGGATGCTGACAT AAT A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:16439263..16439451 26863196 MeRIP-seq:(Medium) rs1561896224 Functional Loss DEL dbSNP153 33..34 33 - - - 68500 RMVar_ID_68500 Human_SNP_ID_268251450 m1A Human chr6 - 16439384 16439382 16439384 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCTT__TCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC AAT A ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1561896224 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68501 RMVar_ID_68501 Human_SNP_ID_268251451 m1A Human chr6 - 16439384 16439383 16439384 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCTT_TTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC AT A ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1263292733 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68502 RMVar_ID_68502 Human_SNP_ID_268251454 m1A Human chr6 - 16439384 16439384 16439384 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCTTTTTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC T A ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1217401435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68503 RMVar_ID_68503 Human_SNP_ID_268251455 m1A Human chr6 - 16439384 16439384 16439384 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCTTGTTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1217401435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68504 RMVar_ID_68504 Human_SNP_ID_268251456 m1A Human chr6 - 16439384 16439384 16439384 GATGTCAGCATCCCCACCCCACCCCAACCCTTATTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC GATGTCAGCATCCCCACCCCACCCCAACCCTTCTTCCCGCCCCGCCCCCGGCCCCGCCCCCCCCC T G ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:16439248..16439400 26863196 MeRIP-seq:(Medium) rs1217401435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68505 RMVar_ID_68505 Human_SNP_ID_268257502 m1A Human chr6 - 16462864 16462864 16462864 AGGTGATGATTTTTGGGGGCCCTGAGAAGCGGACAAGCCATCTGAATAGAGCGGTTTGGGTGCCT AGGTGATGATTTTTGGGGGCCCTGAGAAGCGGGCAAGCCATCTGAATAGAGCGGTTTGGGTGCCT T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:16462747..16462897 26863196 MeRIP-seq:(Medium) rs976580824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840245 RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_365949,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_314570,RMVar_hsa_circ_237281 68506 RMVar_ID_68506 Human_SNP_ID_268281142 m1A Human chr6 - 16563642 16563641 16563642 CTGTGTATCAACTTGAACCCTCACACCCCCCAACTTGGACCTTTCTAAATCTTAAAATCTCAGAC CTGTGTATCAACTTGAACCCTCACACCCCCCA_CTTGGACCTTTCTAAATCTTAAAATCTCAGAC GT G ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:16563515..16563641 26863196 MeRIP-seq:(Medium) rs1353821814 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1666916,Human_RBP_ID_24146723 RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_270232,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_282080,RMVar_hsa_circ_237283,RMVar_hsa_circ_237284,RMVar_hsa_circ_288351,RMVar_hsa_circ_359169,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286 68507 RMVar_ID_68507 Human_SNP_ID_268283549 m1A Human chr6 - 16573495 16573493 16573495 ATGTATGTAGGGTGGCCAGAGTTGGGAGAAACAGGGGACAGGCGAGTCAGGAATTAAAGATAGGT ATGTATGTAGGGTGGCCAGAGTTGGGAGAAAC__GGGACAGGCGAGTCAGGAATTAAAGATAGGT CCT C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:16573444..16573595 26863196 MeRIP-seq:(Medium) rs71965340 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_270232,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_282080,RMVar_hsa_circ_237283,RMVar_hsa_circ_237284,RMVar_hsa_circ_288351,RMVar_hsa_circ_359169,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286 68508 RMVar_ID_68508 Human_SNP_ID_268283552 m1A Human chr6 - 16573495 16573495 16573495 ATGTATGTAGGGTGGCCAGAGTTGGGAGAAACAGGGGACAGGCGAGTCAGGAATTAAAGATAGGT ATGTATGTAGGGTGGCCAGAGTTGGGAGAAACGGGGGACAGGCGAGTCAGGAATTAAAGATAGGT T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:16573444..16573595 26863196 MeRIP-seq:(Medium) rs889998479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_967,RMVar_hsa_circ_94335,RMVar_hsa_circ_237276,RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_320395,RMVar_hsa_circ_320476,RMVar_hsa_circ_270232,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_282080,RMVar_hsa_circ_237283,RMVar_hsa_circ_237284,RMVar_hsa_circ_288351,RMVar_hsa_circ_359169,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286 68509 RMVar_ID_68509 Human_SNP_ID_268327219 m1A Human chr6 - 16753349 16753349 16753349 GATTTCCTCTCCTGCACTCCCTCGACCATTGCAGGAGCATCGTGCATCAAGTCACCAGGGTGGTC GATTTCCTCTCCTGCACTCCCTCGACCATTGCGGGAGCATCGTGCATCAAGTCACCAGGGTGGTC T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:16753311..16753405 26863196 MeRIP-seq:(Medium) rs1458872288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26039941 RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237279,RMVar_hsa_circ_310121,RMVar_hsa_circ_333338,RMVar_hsa_circ_237285,RMVar_hsa_circ_312360,RMVar_hsa_circ_237295,RMVar_hsa_circ_276240,RMVar_hsa_circ_237296,RMVar_hsa_circ_108151,RMVar_hsa_circ_110307,RMVar_hsa_circ_237298,RMVar_hsa_circ_292771,RMVar_hsa_circ_237302,RMVar_hsa_circ_237303,RMVar_hsa_circ_237301 68510 RMVar_ID_68510 Human_SNP_ID_268328956 m1A Human chr6 + 16760136 16760136 16760136 GCCTGCGCGCAGCACTGGAACCACGTAGGAGGAGGCGGCGGCGCCCCCGGGAGTGGCAGAGTCTC GCCTGCGCGCAGCACTGGAACCACGTAGGAGGCGGCGGCGGCGCCCCCGGGAGTGGCAGAGTCTC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:16760064..16760177 26863196 MeRIP-seq:(Medium) rs1035166202 Functional Loss SNV dbSNP153 33..33 33 - - - 68511 RMVar_ID_68511 Human_SNP_ID_268328957 m1A Human chr6 + 16760136 16760136 16760136 GCCTGCGCGCAGCACTGGAACCACGTAGGAGGAGGCGGCGGCGCCCCCGGGAGTGGCAGAGTCTC GCCTGCGCGCAGCACTGGAACCACGTAGGAGGGGGCGGCGGCGCCCCCGGGAGTGGCAGAGTCTC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:16760064..16760177 26863196 MeRIP-seq:(Medium) rs1035166202 Functional Loss SNV dbSNP153 33..33 33 - - - 68512 RMVar_ID_68512 Human_SNP_ID_268329488 m1A Human chr6 - 16761403 16761403 16761403 ACAGGACCTGTTTCACTGCAGGGGGATCCAAAACAAGCCCCGTGGAGCAGCAGCCAGAGCAACAG ACAGGACCTGTTTCACTGCAGGGGGATCCAAAGCAAGCCCCGTGGAGCAGCAGCCAGAGCAACAG T C ATXN1 Ensembl:ENSG00000124788 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:16761266..16761435 26863196 MeRIP-seq:(Medium) rs1340638395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841010,Human_RBP_ID_952099,Human_RBP_ID_5450741,Human_RBP_ID_5477618,Human_RBP_ID_18425359,Human_RBP_ID_18858779 RMVar_hsa_circ_100366,RMVar_hsa_circ_237285,RMVar_hsa_circ_108151,RMVar_hsa_circ_110307,RMVar_hsa_circ_237298,RMVar_hsa_circ_237303,RMVar_hsa_circ_237304,RMVar_hsa_circ_100594 68513 RMVar_ID_68513 Human_SNP_ID_268492192 m1A Human chr6 - 17421493 17421493 17421493 GCGTGAGCATCAGGGAGGATGAGTAAACCAACACCATCAGTCTCAACAACAGCGAGGAGGAAGAC GCGTGAGCATCAGGGAGGATGAGTAAACCAACGCCATCAGTCTCAACAACAGCGAGGAGGAAGAC T C RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:17421490..17421600 26863196 MeRIP-seq:(Medium) rs1036617348 Functional Loss SNV dbSNP153 33..33 33 - - - 68514 RMVar_ID_68514 Human_SNP_ID_268520385 m1A Human chr6 - 17539324 17539324 17539324 CTGGAGGAGGCAGAGGAGGAGGGGGTGGAGGAAGGCCAGGCCCAGAGGAGAGGACAGAAAACGCT CTGGAGGAGGCAGAGGAGGAGGGGGTGGAGGATGGCCAGGCCCAGAGGAGAGGACAGAAAACGCT T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:17539267..17539374 26863196 MeRIP-seq:(Medium) rs1421530567 Functional Loss SNV dbSNP153 33..33 33 - - - 68515 RMVar_ID_68515 Human_SNP_ID_268536438 m1A Human chr6 + 17600429 17600420 17600430 TGCTGAGGCGACGATGGCCGAGGGGCCCGAGGAAGCCCGAGGCCACCCTCCCGGGCAGGACGATG TGCTGAGGCGACGATGGCCGAGGG__________GCCCGAGGCCACCCTCCCGGGCAGGACGATG GGCCCGAGGAA G FAM8A1 Ensembl:ENSG00000137414 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:17600393..17600556 26863196 MeRIP-seq:(Medium) rs1015058766 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_790433,Human_RBP_ID_4874143,Human_RBP_ID_22460926 RMVar_hsa_circ_121154,RMVar_hsa_circ_237323 68516 RMVar_ID_68516 Human_SNP_ID_268536439 m1A Human chr6 + 17600429 17600421 17600430 TGCTGAGGCGACGATGGCCGAGGGGCCCGAGGAAGCCCGAGGCCACCCTCCCGGGCAGGACGATG TGCTGAGGCGACGATGGCCGAGGGG_________GCCCGAGGCCACCCTCCCGGGCAGGACGATG GCCCGAGGAA G FAM8A1 Ensembl:ENSG00000137414 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:17600393..17600556 26863196 MeRIP-seq:(Medium) rs1390453097 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_790433,Human_RBP_ID_4874143,Human_RBP_ID_22460926 RMVar_hsa_circ_121154,RMVar_hsa_circ_237323 68517 RMVar_ID_68517 Human_SNP_ID_268536446 m1A Human chr6 + 17600429 17600429 17600429 TGCTGAGGCGACGATGGCCGAGGGGCCCGAGGAAGCCCGAGGCCACCCTCCCGGGCAGGACGATG TGCTGAGGCGACGATGGCCGAGGGGCCCGAGGGAGCCCGAGGCCACCCTCCCGGGCAGGACGATG A G FAM8A1 Ensembl:ENSG00000137414 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:17600393..17600556 26863196 MeRIP-seq:(Medium) rs1418673907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790433,Human_RBP_ID_4874143,Human_RBP_ID_22460926 RMVar_hsa_circ_121154,RMVar_hsa_circ_237323 68518 RMVar_ID_68518 Human_SNP_ID_268536510 m1A Human chr6 + 17600552 17600552 17600552 ATGCCCCCGCGACGACCCCCAGGCCGAACCCCAGGCCCCGGGCCGGCCCACAGCCCCGGGCCTCG ATGCCCCCGCGACGACCCCCAGGCCGAACCCCCGGCCCCGGGCCGGCCCACAGCCCCGGGCCTCG A C FAM8A1 Ensembl:ENSG00000137414 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:17600453..17600753 26863410 MeRIP-seq:(Medium) rs758577703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904508 RMVar_hsa_circ_121154,RMVar_hsa_circ_237323 68519 RMVar_ID_68519 Human_SNP_ID_268536652 m1A Human chr6 + 17600797 17600797 17600797 AGTGGCTGTGGCAGTCCTACTGCGGCTACCTCACCTGGCACAGCGGCCTGGCCGCCTTCCCAGCC AGTGGCTGTGGCAGTCCTACTGCGGCTACCTCCCCTGGCACAGCGGCCTGGCCGCCTTCCCAGCC A C FAM8A1 Ensembl:ENSG00000137414 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:17600752..17600852 26863196 MeRIP-seq:(Medium) rs780323115 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22104641 RMVar_hsa_circ_121154,RMVar_hsa_circ_237323 68520 RMVar_ID_68520 Human_SNP_ID_268553597 m1A Human chr6 + 17661702 17661702 17661702 TAGAAGCAACAAAGCGTGTTCTTTCTCGTCTCATCTTGCCACCTCCACCACCTACTCCAGAAGAT TAGAAGCAACAAAGCGTGTTCTTTCTCGTCTCGTCTTGCCACCTCCACCACCTACTCCAGAAGAT A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:17661651..17661725 26863196 MeRIP-seq:(Medium) rs1268628411 Functional Loss SNV dbSNP153 33..33 33 - - - 68521 RMVar_ID_68521 Human_SNP_ID_268566691 m1A Human chr6 - 17706320 17706320 17706320 TGGCGGCAAGATCCGGACGCGGCGTTGCCACCAGGGGCCAATTAAGCCTTACCAGCAGGGGCGAC TGGCGGCAAGATCCGGACGCGGCGTTGCCACCGGGGGCCAATTAAGCCTTACCAGCAGGGGCGAC T C NUP153 Ensembl:ENSG00000124789 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:17706256..17706784 32194978 MeRIP-seq:(Medium) rs780264869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968572,Human_RBP_ID_4909231,Human_RBP_ID_5242528,Human_RBP_ID_7578455,Human_RBP_ID_8898777,Human_RBP_ID_22534135,Human_RBP_ID_22615893,Human_RBP_ID_23058343,Human_RBP_ID_27092845 Human_Splice_Rec_740439,Human_Splice_Rec_740479,Human_Splice_Rec_740523 68522 RMVar_ID_68522 Human_SNP_ID_268566692 m1A Human chr6 - 17706320 17706320 17706320 TGGCGGCAAGATCCGGACGCGGCGTTGCCACCAGGGGCCAATTAAGCCTTACCAGCAGGGGCGAC TGGCGGCAAGATCCGGACGCGGCGTTGCCACCCGGGGCCAATTAAGCCTTACCAGCAGGGGCGAC T G NUP153 Ensembl:ENSG00000124789 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:17706256..17706784 32194978 MeRIP-seq:(Medium) rs780264869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968572,Human_RBP_ID_4909231,Human_RBP_ID_5242528,Human_RBP_ID_7578455,Human_RBP_ID_8898777,Human_RBP_ID_22534135,Human_RBP_ID_22615893,Human_RBP_ID_23058343,Human_RBP_ID_27092845 Human_Splice_Rec_740439,Human_Splice_Rec_740479,Human_Splice_Rec_740523 68523 RMVar_ID_68523 Human_SNP_ID_268566815 m1A Human chr6 - 17706575 17706575 17706575 CCTCTGCGGCCGCCACCCCCTTCCCCGCTGCCAGCACTCACCCTCTCTCCGCTCCTGCTCGCAAC CCTCTGCGGCCGCCACCCCCTTCCCCGCTGCCCGCACTCACCCTCTCTCCGCTCCTGCTCGCAAC T G NUP153 Ensembl:ENSG00000124789 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:17706526..17706866 26863196 MeRIP-seq:(Medium) rs1312788895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4874409,Human_RBP_ID_5477658,Human_RBP_ID_5532320 68524 RMVar_ID_68524 Human_SNP_ID_268566906 m1A Human chr6 - 17706846 17706840 17706846 CAACGGCGGCGGAGGCTGCAGGGACGACGACGACGACGGCGGCGGGGCGGGCGCTGTGCGCACAG CAACGGCGGCGGAGGCTGCAGGGACGACGACG______GCGGCGGGGCGGGCGCTGTGCGCACAG CCGTCGT C NUP153 Ensembl:ENSG00000124789 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h chr6:17706534..17706925;chr6:17706762..17706851;chr6:17706539..17706925 26863196,26863410,26863196 MeRIP-seq:(Medium) rs893041007 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4874413 68525 RMVar_ID_68525 Human_SNP_ID_268566907 m1A Human chr6 - 17706846 17706840 17706846 CAACGGCGGCGGAGGCTGCAGGGACGACGACGACGACGGCGGCGGGGCGGGCGCTGTGCGCACAG CAACGGCGGCGGAGGCTGCAGGGACGACGACG___ACGGCGGCGGGGCGGGCGCTGTGCGCACAG CCGTCGT CCGT NUP153 Ensembl:ENSG00000124789 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h chr6:17706534..17706925;chr6:17706762..17706851;chr6:17706539..17706925 26863196,26863410,26863196 MeRIP-seq:(Medium) rs893041007 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4874413 68526 RMVar_ID_68526 Human_SNP_ID_268566911 m1A Human chr6 - 17706843 17706843 17706843 CGGCGGCGGAGGCTGCAGGGACGACGACGACGACGGCGGCGGGGCGGGCGCTGTGCGCACAGGGG CGGCGGCGGAGGCTGCAGGGACGACGACGACGGCGGCGGCGGGGCGGGCGCTGTGCGCACAGGGG T C NUP153 Ensembl:ENSG00000124789 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:17706546..17706899 26863196 MeRIP-seq:(Medium) rs963701919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4874413 68527 RMVar_ID_68527 Human_SNP_ID_268584327 m1A Human chr6 + 17760799 17760799 17760799 CATGTTTTAGAGATGGGGCTGGTGCTTGCCCAAGGTGACCAGGCGAACAAAGACGCCAAGCTGTG CATGTTTTAGAGATGGGGCTGGTGCTTGCCCATGGTGACCAGGCGAACAAAGACGCCAAGCTGTG A T RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:17760776..17760800 26863196 MeRIP-seq:(Medium) rs1303483283 Functional Loss SNV dbSNP153 33..33 33 - - - 68528 RMVar_ID_68528 Human_SNP_ID_268590642 m1A Human chr6 + 17785568 17785568 17785568 ATCCCACTGCCTGGGGCTGGCACCAGCACAGCATTCCTTTCCTCAGTCAGCCCTACCCACTGCTC ATCCCACTGCCTGGGGCTGGCACCAGCACAGCGTTCCTTTCCTCAGTCAGCCCTACCCACTGCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:17785446..17785600 26863196 MeRIP-seq:(Medium) rs1195820549 Functional Loss SNV dbSNP153 33..33 33 - - - 68529 RMVar_ID_68529 Human_SNP_ID_268590653 m1A Human chr6 + 17785602 17785602 17785602 TCCTTTCCTCAGTCAGCCCTACCCACTGCTCCACAAGCTGGGCTTCCCGCTCCACATCGTCCTCT TCCTTTCCTCAGTCAGCCCTACCCACTGCTCCGCAAGCTGGGCTTCCCGCTCCACATCGTCCTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:17785551..17785650 26863196 MeRIP-seq:(Medium) rs1462585050 Functional Loss SNV dbSNP153 33..33 33 - - - 68530 RMVar_ID_68530 Human_SNP_ID_268602631 m1A Human chr6 - 17831224 17831224 17831224 TTTGTCTGTTTTTGTGCACAGGAAAGACAACGACAACTTGAAAGCATGGGGATTTCCCTGGAGAT TTTGTCTGTTTTTGTGCACAGGAAAGACAACGTCAACTTGAAAGCATGGGGATTTCCCTGGAGAT T A KIF13A Ensembl:ENSG00000137177 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:17831174..17831280 26863196 MeRIP-seq:(Medium) rs905830829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80438,Human_RBP_ID_949087,Human_RBP_ID_22683730,Human_RBP_ID_27827339 Human_Splice_Rec_740588,Human_Splice_Rec_740688,Human_Splice_Rec_740762,Human_Splice_Rec_740832,Human_Splice_Rec_740904 RMVar_hsa_circ_7576,RMVar_hsa_circ_61774,RMVar_hsa_circ_121386,RMVar_hsa_circ_110489,RMVar_hsa_circ_237396,RMVar_hsa_circ_86443,RMVar_hsa_circ_237395,RMVar_hsa_circ_237401,RMVar_hsa_circ_32664,RMVar_hsa_circ_102798,RMVar_hsa_circ_237408,RMVar_hsa_circ_237407,RMVar_hsa_circ_55655,RMVar_hsa_circ_83939,RMVar_hsa_circ_237414,RMVar_hsa_circ_100686,RMVar_hsa_circ_237415,RMVar_hsa_circ_363986,RMVar_hsa_circ_377368,RMVar_hsa_circ_65096,RMVar_hsa_circ_306424,RMVar_hsa_circ_68094,RMVar_hsa_circ_354319,RMVar_hsa_circ_71091,RMVar_hsa_circ_64164,RMVar_hsa_circ_306832,RMVar_hsa_circ_237418,RMVar_hsa_circ_237419,RMVar_hsa_circ_378496,RMVar_hsa_circ_237422,RMVar_hsa_circ_301183,RMVar_hsa_circ_237421,RMVar_hsa_circ_237424,RMVar_hsa_circ_293666,RMVar_hsa_circ_317996,RMVar_hsa_circ_378583,RMVar_hsa_circ_17466,RMVar_hsa_circ_9089,RMVar_hsa_circ_237423,RMVar_hsa_circ_322771,RMVar_hsa_circ_237425 68531 RMVar_ID_68531 Human_SNP_ID_268637643 m1A Human chr6 + 17975265 17975265 17975265 ATCCCAGCTACTCGGAAGGCTCAGGCAGGAGAATTGTTTGAATCTGGGAGGTGAAGGTTGCAATG ATCCCAGCTACTCGGAAGGCTCAGGCAGGAGACTTGTTTGAATCTGGGAGGTGAAGGTTGCAATG A C RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:17975263..17975429 26863196 MeRIP-seq:(Medium) rs1402773871 Functional Loss SNV dbSNP153 33..33 33 - - - 68532 RMVar_ID_68532 Human_SNP_ID_268637647 m1A Human chr6 - 17975269 17975269 17975269 AGCTCATTGCAACCTTCACCTCCCAGATTCAAACAATTCTCCTGCCTGAGCCTTCCGAGTAGCTG AGCTCATTGCAACCTTCACCTCCCAGATTCAATCAATTCTCCTGCCTGAGCCTTCCGAGTAGCTG T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:17975267..17975382 26863196 MeRIP-seq:(Medium) rs906944757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 68533 RMVar_ID_68533 Human_SNP_ID_268637648 m1A Human chr6 - 17975269 17975269 17975269 AGCTCATTGCAACCTTCACCTCCCAGATTCAAACAATTCTCCTGCCTGAGCCTTCCGAGTAGCTG AGCTCATTGCAACCTTCACCTCCCAGATTCAACCAATTCTCCTGCCTGAGCCTTCCGAGTAGCTG T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:17975267..17975382 26863196 MeRIP-seq:(Medium) rs906944757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 68534 RMVar_ID_68534 Human_SNP_ID_268641185 m1A Human chr6 - 17987127 17987127 17987127 TCTCTCTGCTTTCAGAACTGGAACTGAACACCAAGTGCGTGGTGGAGATGGAAGGGAATCAAACG TCTCTCTGCTTTCAGAACTGGAACTGAACACCCAGTGCGTGGTGGAGATGGAAGGGAATCAAACG T G KIF13A Ensembl:ENSG00000137177 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:17987076..17987195 26863196 MeRIP-seq:(Medium) rs945806990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4874489,Human_RBP_ID_9399988,Human_RBP_ID_22553526,Human_RBP_ID_22683732,Human_RBP_ID_26353435 Human_Splice_Rec_740566,Human_Splice_Rec_740567,Human_Splice_Rec_740666,Human_Splice_Rec_740667,Human_Splice_Rec_740740,Human_Splice_Rec_740741,Human_Splice_Rec_740810,Human_Splice_Rec_740811,Human_Splice_Rec_740882,Human_Splice_Rec_740883,Human_Splice_Rec_741018,Human_Splice_Rec_741019,Human_Splice_Rec_741025,Human_Splice_Rec_741030,Human_Splice_Rec_741031 RMVar_hsa_circ_7576 68535 RMVar_ID_68535 Human_SNP_ID_268641322 m1A Human chr6 - 17987487 17987467 17987488 GAGGGGCCGCCTAAGGCCGAGCGGGCGCGGCGAGCGGCCGGGCGAGCGCAGCCAACATGTCGGAT GAGGGGCCGCCTAAGGCCGAGCGGGCGCGGC_____________________CAACATGTCGGAT GGCTGCGCTCGCCCGGCCGCTC G KIF13A Ensembl:ENSG00000137177 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:17987401..17987601 26863196 MeRIP-seq:(Medium) rs745874698 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_4903119,Human_RBP_ID_8905121,Human_RBP_ID_9309112,Human_RBP_ID_18425576 Human_Splice_Rec_740565,Human_Splice_Rec_740665,Human_Splice_Rec_740739,Human_Splice_Rec_740809,Human_Splice_Rec_740881,Human_Splice_Rec_741017,Human_Splice_Rec_741029 68536 RMVar_ID_68536 Human_SNP_ID_268641337 m1A Human chr6 - 17987487 17987487 17987487 GAGGGGCCGCCTAAGGCCGAGCGGGCGCGGCGAGCGGCCGGGCGAGCGCAGCCAACATGTCGGAT GAGGGGCCGCCTAAGGCCGAGCGGGCGCGGCGTGCGGCCGGGCGAGCGCAGCCAACATGTCGGAT T A KIF13A Ensembl:ENSG00000137177 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:17987401..17987601 26863196 MeRIP-seq:(Medium) rs1468305198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903119,Human_RBP_ID_8905121,Human_RBP_ID_9309112,Human_RBP_ID_18425576 Human_Splice_Rec_740565,Human_Splice_Rec_740665,Human_Splice_Rec_740739,Human_Splice_Rec_740809,Human_Splice_Rec_740881,Human_Splice_Rec_741017,Human_Splice_Rec_741029 68537 RMVar_ID_68537 Human_SNP_ID_268641478 m1A Human chr6 - 17987796 17987786 17987797 GGCGCGGAACATGGCGGCGCGGGGCCCCGGGCAGCCGCGAGGGGCCGCGGCGCTGCGGTCTCGGC GGCGCGGAACATGGCGGCGCGGGGCCCCGGG___________GGCCGCGGCGCTGCGGTCTCGGC CCCTCGCGGCTG C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:17987759..17987858 26863196 MeRIP-seq:(Medium) rs1220087547 Functional Loss DEL dbSNP153 32..42 33 - - - 68538 RMVar_ID_68538 Human_SNP_ID_268700235 m1A Human chr6 + 18205639 18205639 18205639 GGTGCTTCAGTTCCATCTCAGTAACCTGGAGTACGCCTGTGGCAGCAACCTTCACCAGGTGCGCT GGTGCTTCAGTTCCATCTCAGTAACCTGGAGTGCGCCTGTGGCAGCAACCTTCACCAGGTGCGCT A G KDM1B Ensembl:ENSG00000165097 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:18205591..18207524 32194978 MeRIP-seq:(Medium) rs760788771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3969559,Human_RBP_ID_8905124,Human_RBP_ID_9309533 Human_Splice_Rec_741083,Human_Splice_Rec_741125 RMVar_hsa_circ_5573,RMVar_hsa_circ_265720,RMVar_hsa_circ_346435,RMVar_hsa_circ_268976,RMVar_hsa_circ_84289,RMVar_hsa_circ_237441,RMVar_hsa_circ_117298,RMVar_hsa_circ_237440,RMVar_hsa_circ_267955,RMVar_hsa_circ_237452,RMVar_hsa_circ_112208,RMVar_hsa_circ_237468,RMVar_hsa_circ_16681,RMVar_hsa_circ_75600,RMVar_hsa_circ_237456,RMVar_hsa_circ_237457,RMVar_hsa_circ_237459,RMVar_hsa_circ_29908,RMVar_hsa_circ_237461,RMVar_hsa_circ_352414,RMVar_hsa_circ_17013,RMVar_hsa_circ_343368,RMVar_hsa_circ_237464,RMVar_hsa_circ_347005,RMVar_hsa_circ_374967,RMVar_hsa_circ_308114,RMVar_hsa_circ_237470,RMVar_hsa_circ_12094,RMVar_hsa_circ_237469,RMVar_hsa_circ_81345,RMVar_hsa_circ_237467,RMVar_hsa_circ_70176,RMVar_hsa_circ_237471,RMVar_hsa_circ_237472,RMVar_hsa_circ_123828,RMVar_hsa_circ_57082,RMVar_hsa_circ_341192 68539 RMVar_ID_68539 Human_SNP_ID_268711383 m1A Human chr6 + 18243488 18243488 18243488 AGCATGGGTTCAACCTACATTACCTTAGTTTCATCTCTCATTGCTCTACTTCTGGGCACACAACT AGCATGGGTTCAACCTACATTACCTTAGTTTCCTCTCTCATTGCTCTACTTCTGGGCACACAACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:18243486..18243600 26863196 MeRIP-seq:(Medium) rs1173129111 Functional Loss SNV dbSNP153 33..33 33 - - - 68540 RMVar_ID_68540 Human_SNP_ID_268713062 m1A Human chr6 - 18249612 18249612 18249612 TATTTTACTATATTTTTAAATCATTTCTTTCCATGGGGAGAGTTAAATATTTCTGCTATAAGGTA TATTTTACTATATTTTTAAATCATTTCTTTCCGTGGGGAGAGTTAAATATTTCTGCTATAAGGTA T C DEK Ensembl:ENSG00000124795 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:18249610..18249792 26863196 MeRIP-seq:(Medium) rs756795891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80146,Human_RBP_ID_5242661,Human_RBP_ID_5398488,Human_RBP_ID_15753743,Human_RBP_ID_18413824,Human_RBP_ID_22365462,Human_RBP_ID_24436624 RMVar_hsa_circ_62800,RMVar_hsa_circ_348771,RMVar_hsa_circ_358479,RMVar_hsa_circ_297759,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,RMVar_hsa_circ_237483,RMVar_hsa_circ_10389,RMVar_hsa_circ_65487,RMVar_hsa_circ_317221,RMVar_hsa_circ_237485 68541 RMVar_ID_68541 Human_SNP_ID_268713108 m1A Human chr6 - 18249751 18249751 18249751 TTCTGGAATGGCAAGGAAGGCTAAGCGAACCAAATGTCCTGAAATTCTGTCAGATGAATCTAGTA TTCTGGAATGGCAAGGAAGGCTAAGCGAACCAGATGTCCTGAAATTCTGTCAGATGAATCTAGTA T C DEK Ensembl:ENSG00000124795 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:18249701..18249775 32194978 MeRIP-seq:(Medium) rs1231177081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658285,Human_RBP_ID_1668093,Human_RBP_ID_2015677,Human_RBP_ID_3802577,Human_RBP_ID_4874664,Human_RBP_ID_5622280,Human_RBP_ID_7579287,Human_RBP_ID_8898819,Human_RBP_ID_9192358,Human_RBP_ID_9399997,Human_RBP_ID_10274994,Human_RBP_ID_15753744,Human_RBP_ID_18070415,Human_RBP_ID_18859689,Human_RBP_ID_24150773,Human_RBP_ID_24387559,Human_RBP_ID_24548543,Human_RBP_ID_26354757,Human_RBP_ID_27827346 Human_Splice_Rec_741192,Human_Splice_Rec_741214,Human_Splice_Rec_741232,Human_Splice_Rec_741252,Human_Splice_Rec_741274,Human_Splice_Rec_741292,Human_Splice_Rec_741312,Human_Splice_Rec_741330,Human_Splice_Rec_741342 Human_miRNA_ID_2626099,Human_miRNA_ID_2746921 RMVar_hsa_circ_6526,RMVar_hsa_circ_62800,RMVar_hsa_circ_348771,RMVar_hsa_circ_358479,RMVar_hsa_circ_297759,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,RMVar_hsa_circ_237483,RMVar_hsa_circ_10389,RMVar_hsa_circ_65487,RMVar_hsa_circ_317221,RMVar_hsa_circ_283292,RMVar_hsa_circ_237485,RMVar_hsa_circ_64068,RMVar_hsa_circ_237486,RMVar_hsa_circ_6000 68542 RMVar_ID_68542 Human_SNP_ID_268715622 m1A Human chr6 - 18258404 18258404 18258404 GTTAATTAAGAAATACTAAATTAATTTCTAGAAAAGAGTCTCATCGTGGAAGGCAAGAGGGAAAA GTTAATTAAGAAATACTAAATTAATTTCTAGAGAAGAGTCTCATCGTGGAAGGCAAGAGGGAAAA T C DEK Ensembl:ENSG00000124795 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr6:18258301..18264550;chr6:18258301..18258443;chr6:18257951..18264550;chr6:18258301..18258425 26863196,32194978 MeRIP-seq:(Medium) rs777336855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658313,Human_RBP_ID_792139,Human_RBP_ID_2997433,Human_RBP_ID_7579424,Human_RBP_ID_23116418,Human_RBP_ID_24150816,Human_RBP_ID_24548544,Human_RBP_ID_26353441 Human_Splice_Rec_741184,Human_Splice_Rec_741210,Human_Splice_Rec_741224,Human_Splice_Rec_741244,Human_Splice_Rec_741266,Human_Splice_Rec_741284,Human_Splice_Rec_741285,Human_Splice_Rec_741322,Human_Splice_Rec_741346,Human_Splice_Rec_741356 RMVar_hsa_circ_62800,RMVar_hsa_circ_358479,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,RMVar_hsa_circ_65487,RMVar_hsa_circ_317221,RMVar_hsa_circ_283292,RMVar_hsa_circ_237485,RMVar_hsa_circ_64068,RMVar_hsa_circ_27303,RMVar_hsa_circ_237486,RMVar_hsa_circ_237487,RMVar_hsa_circ_68404,RMVar_hsa_circ_272868,RMVar_hsa_circ_237488,RMVar_hsa_circ_296652,RMVar_hsa_circ_361870 68543 RMVar_ID_68543 Human_SNP_ID_268717383 m1A Human chr6 + 18263811 18263811 18263811 GGGTGAAAAATACAAAAAAACTTCGGTCTGAAAAATTCATCAGTTGGGATGCGACTCCCCCCACC GGGTGAAAAATACAAAAAAACTTCGGTCTGAACAATTCATCAGTTGGGATGCGACTCCCCCCACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:18263809..18264550 26863196 MeRIP-seq:(Medium) rs370413497 Functional Loss SNV dbSNP153 33..33 33 - - - 68544 RMVar_ID_68544 Human_SNP_ID_268717451 m1A Human chr6 - 18263894 18263894 18263894 AAGAACCCGAAATGCCCGGTCCCAGAGAGGAGAGCGAGGAGGAAGAGGACGAGGACGACGAGGAG AAGAACCCGAAATGCCCGGTCCCAGAGAGGAGTGCGAGGAGGAAGAGGACGAGGACGACGAGGAG T A DEK Ensembl:ENSG00000124795 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:18263826..18263900 26863196 MeRIP-seq:(Medium) rs765097595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658314,Human_RBP_ID_4874690,Human_RBP_ID_7579551,Human_RBP_ID_8943995,Human_RBP_ID_23067769,Human_RBP_ID_23120265,Human_RBP_ID_24150851,Human_RBP_ID_26354764,Human_RBP_ID_27092933 Human_Splice_Rec_741183,Human_Splice_Rec_741209,Human_Splice_Rec_741223,Human_Splice_Rec_741243,Human_Splice_Rec_741265,Human_Splice_Rec_741283,Human_Splice_Rec_741305,Human_Splice_Rec_741321,Human_Splice_Rec_741355 Human_miRNA_ID_1192561 RMVar_hsa_circ_62800,RMVar_hsa_circ_358479,RMVar_hsa_circ_65487,RMVar_hsa_circ_64068,RMVar_hsa_circ_27303,RMVar_hsa_circ_68404 68545 RMVar_ID_68545 Human_SNP_ID_268717478 m1A Human chr6 - 18263927 18263927 18263927 GGGAGGGAACCCCCACCCAGCCCGCGTCCGAGAAAGAACCCGAAATGCCCGGTCCCAGAGAGGAG GGGAGGGAACCCCCACCCAGCCCGCGTCCGAGGAAGAACCCGAAATGCCCGGTCCCAGAGAGGAG T C DEK Ensembl:ENSG00000124795 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:18263876..18264550 26863196 MeRIP-seq:(Medium) rs776208437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4874690,Human_RBP_ID_15754416,Human_RBP_ID_23058509 Human_Splice_Rec_741182,Human_Splice_Rec_741183,Human_Splice_Rec_741208,Human_Splice_Rec_741209,Human_Splice_Rec_741223,Human_Splice_Rec_741242,Human_Splice_Rec_741243,Human_Splice_Rec_741264,Human_Splice_Rec_741265,Human_Splice_Rec_741282,Human_Splice_Rec_741283,Human_Splice_Rec_741304,Human_Splice_Rec_741305,Human_Splice_Rec_741321,Human_Splice_Rec_741354,Human_Splice_Rec_741355 RMVar_hsa_circ_62800,RMVar_hsa_circ_358479,RMVar_hsa_circ_65487,RMVar_hsa_circ_64068,RMVar_hsa_circ_27303,RMVar_hsa_circ_68404 68546 RMVar_ID_68546 Human_SNP_ID_268717751 m1A Human chr6 - 18264409 18264409 18264409 CCTCCCAGAACCTCCTCGTGCCCTCGCGTGCCAGGCCCGCGGCGGCCGAAATCCGCGGTAAGGGC CCTCCCAGAACCTCCTCGTGCCCTCGCGTGCCGGGCCCGCGGCGGCCGAAATCCGCGGTAAGGGC T C DEK Ensembl:ENSG00000124795 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:18264376..18264500 32194978 MeRIP-seq:(Medium) rs1223205968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792142,Human_RBP_ID_1394474,Human_RBP_ID_4874696,Human_RBP_ID_5478652,Human_RBP_ID_18859723,Human_RBP_ID_27092936,Human_RBP_ID_27828303 Human_Splice_Rec_741181,Human_Splice_Rec_741207,Human_Splice_Rec_741241,Human_Splice_Rec_741263,Human_Splice_Rec_741281,Human_Splice_Rec_741303,Human_Splice_Rec_741345,Human_Splice_Rec_741353 68547 RMVar_ID_68547 Human_SNP_ID_268717801 m1A Human chr6 - 18264485 18264485 18264485 GGGAGCCGAGCGCGCGGCGCGAGCGTCACGCCAGACAGCGGCCCGCGCGCCTTCTCCTCGGCGTC GGGAGCCGAGCGCGCGGCGCGAGCGTCACGCCGGACAGCGGCCCGCGCGCCTTCTCCTCGGCGTC T C DEK Ensembl:ENSG00000124795 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:18264151..18264550 26863410 MeRIP-seq:(Medium) rs752008938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252189,Human_RBP_ID_4874697,Human_RBP_ID_9400005,Human_RBP_ID_18425578,Human_RBP_ID_18859724,Human_RBP_ID_22461612,Human_RBP_ID_22531778 68548 RMVar_ID_68548 Human_SNP_ID_268717930 m1A Human chr6 + 18264699 18264699 18264699 CGCGAGGGGTCGCCTCGGCCGCGGGCGGAGGGATGCGCGCGCGGGGCTCTCCCCGGCTGCGCCTG CGCGAGGGGTCGCCTCGGCCGCGGGCGGAGGGTTGCGCGCGCGGGGCTCTCCCCGGCTGCGCCTG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:18264624..18264724 26863410 MeRIP-seq:(Medium) rs900577402 Functional Loss SNV dbSNP153 33..33 33 - - - 68549 RMVar_ID_68549 Human_SNP_ID_268749609 m1A Human chr6 - 18387538 18387538 18387538 CGCCAGTCCGGGCTGCTGGCACACCGGACAGGAGCTCTTCCATTCTCTCCGTCTTTCCTCCGTGC CGCCAGTCCGGGCTGCTGGCACACCGGACAGGCGCTCTTCCATTCTCTCCGTCTTTCCTCCGTGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:18387476..18387664 26863196 MeRIP-seq:(Medium) rs1476311156 Functional Loss SNV dbSNP153 33..33 33 - - - 68550 RMVar_ID_68550 Human_SNP_ID_268749621 m1A Human chr6 + 18387557 18387557 18387557 AGAATGGAAGAGCTCCTGTCCGGTGTGCCAGCAGCCCGGACTGGCGGTGAGCGCGAGGGAGGCTA AGAATGGAAGAGCTCCTGTCCGGTGTGCCAGCCGCCCGGACTGGCGGTGAGCGCGAGGGAGGCTA A C RNF144B Ensembl:ENSG00000137393 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:18387509..18387618 26863196 MeRIP-seq:(Medium) rs1298176760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19017817 Human_Splice_Rec_741359,Human_Splice_Rec_741373 RMVar_hsa_circ_75292 68551 RMVar_ID_68551 Human_SNP_ID_268749625 m1A Human chr6 + 18387564 18387564 18387564 AAGAGCTCCTGTCCGGTGTGCCAGCAGCCCGGACTGGCGGTGAGCGCGAGGGAGGCTACTGAGAA AAGAGCTCCTGTCCGGTGTGCCAGCAGCCCGGGCTGGCGGTGAGCGCGAGGGAGGCTACTGAGAA A G RNF144B Ensembl:ENSG00000137393 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:18387519..18387592 26863196 MeRIP-seq:(Medium) rs766520861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19017817 Human_Splice_Rec_741359,Human_Splice_Rec_741373 RMVar_hsa_circ_75292 68552 RMVar_ID_68552 Human_SNP_ID_268749626 m1A Human chr6 + 18387564 18387564 18387564 AAGAGCTCCTGTCCGGTGTGCCAGCAGCCCGGACTGGCGGTGAGCGCGAGGGAGGCTACTGAGAA AAGAGCTCCTGTCCGGTGTGCCAGCAGCCCGGTCTGGCGGTGAGCGCGAGGGAGGCTACTGAGAA A T RNF144B Ensembl:ENSG00000137393 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:18387519..18387592 26863196 MeRIP-seq:(Medium) rs766520861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19017817 Human_Splice_Rec_741359,Human_Splice_Rec_741373 RMVar_hsa_circ_75292 68553 RMVar_ID_68553 Human_SNP_ID_268752452 m1A Human chr6 + 18399449 18399449 18399449 GATCAGCTGGCCTCCAGACGTGTTGGCTAAACAATAGCTTTATCAATCCATATAATATTTTCTGC GATCAGCTGGCCTCCAGACGTGTTGGCTAAACGATAGCTTTATCAATCCATATAATATTTTCTGC A G RNF144B Ensembl:ENSG00000137393 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:18399444..18399521 26863196 MeRIP-seq:(Medium) rs1304578407 Functional Loss SNV dbSNP153 33..33 33 - - - 68554 RMVar_ID_68554 Human_SNP_ID_268755243 m1A Human chr6 - 18410725 18410722 18410726 CCGACGCCATCCTCCCTATCTCATTCCCAAACAAAGCCTTCCAGTGGCTCCATAATGTTTTTTTA CCGACGCCATCCTCCCTATCTCATTCCCAAA____GCCTTCCAGTGGCTCCATAATGTTTTTTTA CTTTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:18410676..18410838 26863196 MeRIP-seq:(Medium) rs1410606306 Functional Loss DEL dbSNP153 32..35 33 - - - 68555 RMVar_ID_68555 Human_SNP_ID_269108118 m1A Human chr6 - 19837501 19837501 19837501 GAAAAAAAAAGCAAAAGCACCGGAAGAAAAGTAGCCCACCCGGGTGTCCTAGTCACTCCCTTCGG GAAAAAAAAAGCAAAAGCACCGGAAGAAAAGTGGCCCACCCGGGTGTCCTAGTCACTCCCTTCGG T C LNC-LBCS Ensembl:ENSG00000228412 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:19837401..19837550 26863410 MeRIP-seq:(Medium) rs1426029316 Functional Loss SNV dbSNP153 33..33 33 - - - 68556 RMVar_ID_68556 Human_SNP_ID_269108232 m1A Human chr6 + 19837738 19837731 19837738 CCTCGCTCGCCCCAGCGGGTTCGCTCGCGTAGAGCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC CCTCGCTCGCCCCAGCGGGTTCGCTC_______GCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC CGCGTAGA C ID4 Ensembl:ENSG00000172201 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:19837645..19838025 26863410 MeRIP-seq:(Medium) rs775698057 Functional Loss DEL dbSNP153 27..33 33 - - - 68557 RMVar_ID_68557 Human_SNP_ID_269108239 m1A Human chr6 + 19837738 19837738 19837738 CCTCGCTCGCCCCAGCGGGTTCGCTCGCGTAGAGCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC CCTCGCTCGCCCCAGCGGGTTCGCTCGCGTAGGGCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC A G ID4 Ensembl:ENSG00000172201 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:19837645..19838025 26863410 MeRIP-seq:(Medium) rs12662234 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 68558 RMVar_ID_68558 Human_SNP_ID_269108303 m1A Human chr6 + 19837871 19837866 19837872 GCCGAGCACGGCCACAGCCTGGGTGGCTCCGCAGCCGCGGCGGCGGCGGCGGCGGCAGCGCGCTG GCCGAGCACGGCCACAGCCTGGGTGGCT______CCGCGGCGGCGGCGGCGGCGGCAGCGCGCTG TCCGCAG T ID4 Ensembl:ENSG00000172201 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:19837834..19838134 32194978 MeRIP-seq:(Medium) rs901476494 Functional Loss DEL dbSNP153 29..34 33 - - - 68559 RMVar_ID_68559 Human_SNP_ID_269108309 m1A Human chr6 + 19837871 19837871 19837871 GCCGAGCACGGCCACAGCCTGGGTGGCTCCGCAGCCGCGGCGGCGGCGGCGGCGGCAGCGCGCTG GCCGAGCACGGCCACAGCCTGGGTGGCTCCGCGGCCGCGGCGGCGGCGGCGGCGGCAGCGCGCTG A G ID4 Ensembl:ENSG00000172201 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:19837834..19838134 32194978 MeRIP-seq:(Medium) rs903730662 Functional Loss SNV dbSNP153 33..33 33 - - - 68560 RMVar_ID_68560 Human_SNP_ID_269197486 m1A Human chr6 + 20206852 20206852 20206852 TCAGGCGCACACCCCGATTTTCATCATCACCCAGAAAGACTTCACTAGAAATCCTTCACTCACAT TCAGGCGCACACCCCGATTTTCATCATCACCCGGAAAGACTTCACTAGAAATCCTTCACTCACAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20206832..20206952 26863196 MeRIP-seq:(Medium) rs1375202959 Functional Loss SNV dbSNP153 33..33 33 - - - 68561 RMVar_ID_68561 Human_SNP_ID_269197507 m1A Human chr6 - 20206950 20206950 20206950 AGTAGTTGGTGGTGGTAAGAGTGAAGAGGAAAACTTCTTGCGATGGTGGGTCGTGGAGGGCAGGT AGTAGTTGGTGGTGGTAAGAGTGAAGAGGAAAGCTTCTTGCGATGGTGGGTCGTGGAGGGCAGGT T C MBOAT1 Ensembl:ENSG00000172197 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:20206831..20206960 26863196 MeRIP-seq:(Medium) rs1484372218 Functional Loss SNV dbSNP153 33..33 33 - - - 68562 RMVar_ID_68562 Human_SNP_ID_269250231 m1A Human chr6 + 20402469 20402469 20402469 TCCTGTTCCTCCTCCCTCCAAAGCGGCGCCGTAGCCGCCGGCCCCCTCCTCCCCAGTGCCCCCGG TCCTGTTCCTCCTCCCTCCAAAGCGGCGCCGTCGCCGCCGGCCCCCTCCTCCCCAGTGCCCCCGG A C E2F3 Ensembl:ENSG00000112242 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:20402428..20402563 26863196 MeRIP-seq:(Medium) rs749613821 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_27343535 RMVar_hsa_circ_237505,RMVar_hsa_circ_112540 68563 RMVar_ID_68563 Human_SNP_ID_269250232 m1A Human chr6 + 20402469 20402469 20402469 TCCTGTTCCTCCTCCCTCCAAAGCGGCGCCGTAGCCGCCGGCCCCCTCCTCCCCAGTGCCCCCGG TCCTGTTCCTCCTCCCTCCAAAGCGGCGCCGTTGCCGCCGGCCCCCTCCTCCCCAGTGCCCCCGG A T E2F3 Ensembl:ENSG00000112242 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:20402428..20402563 26863196 MeRIP-seq:(Medium) rs749613821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27343535 RMVar_hsa_circ_237505,RMVar_hsa_circ_112540 68564 RMVar_ID_68564 Human_SNP_ID_269250242 m1A Human chr6 - 20402483 20402480 20402483 CGGTCTGCTCCGCGCCGGGGGCACTGGGGAGGAGGGGGCCGGCGGCTACGGCGCCGCTTTGGAGG CGGTCTGCTCCGCGCCGGGGGCACTGGGGAGG___GGGCCGGCGGCTACGGCGCCGCTTTGGAGG CCCT C lnc-MBOAT1-10,RF00017-4643 RNACentral:URS00008BE3DE,RNACentral:URS00009A02E8 lincRNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:20402432..20403862 26863196 MeRIP-seq:(Medium) rs757483296 Functional Loss DEL dbSNP153 33..35 33 - - - 68565 RMVar_ID_68565 Human_SNP_ID_269250552 m1A Human chr6 - 20403266 20403266 20403266 CCAGCCCGCGAGCCCCTCACCCCAGACAGCCCACGCCCCAGTCCGCACCCGGCTTCCAGCCCCAC CCAGCCCGCGAGCCCCTCACCCCAGACAGCCCGCGCCCCAGTCCGCACCCGGCTTCCAGCCCCAC T C lnc-MBOAT1-10,RF00017-4643 RNACentral:URS00008BE3DE,RNACentral:URS00009A02E8 lincRNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:20403264..20403405 26863196 MeRIP-seq:(Medium) rs1339470328 Functional Loss SNV dbSNP153 33..33 33 - - - 68566 RMVar_ID_68566 Human_SNP_ID_269250664 m1A Human chr6 - 20403638 20403638 20403638 CGGGTGCGAGGGCGCCGGGACCGTCCCAGGCCAGGGAGCCGGCGAGCAGGAGGAAGTGGGTGCCC CGGGTGCGAGGGCGCCGGGACCGTCCCAGGCCGGGGAGCCGGCGAGCAGGAGGAAGTGGGTGCCC T C lnc-MBOAT1-10,RF00017-4643 RNACentral:URS00008BE3DE,RNACentral:URS00009A02E8 lincRNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:20403619..20403751 26863196 MeRIP-seq:(Medium) rs937781833 Functional Loss SNV dbSNP153 33..33 33 - - - 68567 RMVar_ID_68567 Human_SNP_ID_269281465 m1A Human chr6 + 20534522 20534522 20534522 CTCTCCATCTAAAGTCTGTGCAGCTTCCGGAGAGTGGCGGGTTGATTTTCTCACTTTGGACTGGT CTCTCCATCTAAAGTCTGTGCAGCTTCCGGAGGGTGGCGGGTTGATTTTCTCACTTTGGACTGGT A G CDKAL1 Ensembl:ENSG00000145996 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr6:20534479..20534573;chr6:20534474..20534610 26863196 MeRIP-seq:(Medium) rs1275192313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18425366,Human_RBP_ID_24151439 Human_Splice_Rec_741707,Human_Splice_Rec_741737 68568 RMVar_ID_68568 Human_SNP_ID_269281473 m1A Human chr6 - 20534536 20534536 20534536 GTCGGGAAGTAAAAACCAGTCCAAAGTGAGAAAATCAACCCGCCACTCTCCGGAAGCTGCACAGA GTCGGGAAGTAAAAACCAGTCCAAAGTGAGAAGATCAACCCGCCACTCTCCGGAAGCTGCACAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:20534486..20534665 26863196 MeRIP-seq:(Medium) rs1268101920 Functional Loss SNV dbSNP153 33..33 33 - - - 68569 RMVar_ID_68569 Human_SNP_ID_269281475 m1A Human chr6 - 20534540 20534539 20534540 AGAAGTCGGGAAGTAAAAACCAGTCCAAAGTGAGAAAATCAACCCGCCACTCTCCGGAAGCTGCA AGAAGTCGGGAAGTAAAAACCAGTCCAAAGTG_GAAAATCAACCCGCCACTCTCCGGAAGCTGCA CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20534490..20534697 26863196 MeRIP-seq:(Medium) rs1349100925 Functional Loss DEL dbSNP153 33..33 33 - - - 68570 RMVar_ID_68570 Human_SNP_ID_269281476 m1A Human chr6 + 20534542 20534542 20534542 CAGCTTCCGGAGAGTGGCGGGTTGATTTTCTCACTTTGGACTGGTTTTTACTTCCCGACTTCTGG CAGCTTCCGGAGAGTGGCGGGTTGATTTTCTCGCTTTGGACTGGTTTTTACTTCCCGACTTCTGG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:20534491..20534684 26863196 MeRIP-seq:(Medium) rs1045491505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948538,Human_RBP_ID_2016090,Human_RBP_ID_4875094,Human_RBP_ID_17305858,Human_RBP_ID_17535021,Human_RBP_ID_18425366,Human_RBP_ID_18859926,Human_RBP_ID_22104666 Human_Splice_Rec_741707,Human_Splice_Rec_741737 68571 RMVar_ID_68571 Human_SNP_ID_269324456 m1A Human chr6 + 20716401 20716401 20716401 AGTTTGTGAAGAGCTGGGGAATGAGATTTTTTAAAATTATCCTGCTGTTGGACAGAAAGTACAGC AGTTTGTGAAGAGCTGGGGAATGAGATTTTTTTAAATTATCCTGCTGTTGGACAGAAAGTACAGC A T CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20716397..20716486 26863196 MeRIP-seq:(Medium) rs1217821385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 68572 RMVar_ID_68572 Human_SNP_ID_269324592 m1A Human chr6 + 20716894 20716894 20716894 AGAGAATGTGGGAAGGCAGAGAAGAGAGAACCAAGGACTAAGAATGTGCTCAGGAGGTTGAGGAG AGAGAATGTGGGAAGGCAGAGAAGAGAGAACCGAGGACTAAGAATGTGCTCAGGAGGTTGAGGAG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:20716872..20716993 26863196 MeRIP-seq:(Medium) rs897812005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15761478 RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 68573 RMVar_ID_68573 Human_SNP_ID_269324638 m1A Human chr6 + 20717073 20717073 20717073 TGAAGATTGACTTACTGGATTTGTCAATAGGGAACTGGTGGTTGTTCTGATGAGCAGTTTCAGTG TGAAGATTGACTTACTGGATTTGTCAATAGGGGACTGGTGGTTGTTCTGATGAGCAGTTTCAGTG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20717069..20717187 26863196 MeRIP-seq:(Medium) rs926193160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 68574 RMVar_ID_68574 Human_SNP_ID_269327831 m1A Human chr6 + 20730309 20730304 20730310 ATGGAGCCACACCCTGAAAAAAAAAGAAAGAAAGAGAAAGAAAAGAAAAGAAAGAAAGAAGCCAG ATGGAGCCACACCCTGAAAAAAAAAGAA______AGAAAGAAAAGAAAAGAAAGAAAGAAGCCAG AAGAAAG A CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20730290..20730553 26863196 MeRIP-seq:(Medium) rs1006232771 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 68575 RMVar_ID_68575 Human_SNP_ID_269327861 m1A Human chr6 + 20730386 20730386 20730386 AGAAAGATAGATAGATGGAGCCCGACCCGAAAAAAAAGGAAGAAAGGAAGAAAGAGAAAGAAAGA AGAAAGATAGATAGATGGAGCCCGACCCGAAAGAAAAGGAAGAAAGGAAGAAAGAGAAAGAAAGA A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:20730362..20730545 26863196 MeRIP-seq:(Medium) rs1317835926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 68576 RMVar_ID_68576 Human_SNP_ID_269532471 m1A Human chr6 - 21587369 21587369 21587369 AGGCGGAGGAAGAAAGGCGCTTGATTGCGGGGAAGTGGGAAGGCACGGAGACCGCATTGGCTGCT AGGCGGAGGAAGAAAGGCGCTTGATTGCGGGGTAGTGGGAAGGCACGGAGACCGCATTGGCTGCT T A AL512380.2 Ensembl:ENSG00000283480 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21587320..21587446 26863196 MeRIP-seq:(Medium) rs1245747282 Functional Loss SNV dbSNP153 33..33 33 - - - 68577 RMVar_ID_68577 Human_SNP_ID_269534115 m1A Human chr6 + 21594108 21594108 21594108 GAGCTACCGAGAGCGCTCGTGAACTGGAATCAACTGCTTCAGGGAAAAAGAAAAAAAAAAAAAAA GAGCTACCGAGAGCGCTCGTGAACTGGAATCAGCTGCTTCAGGGAAAAAGAAAAAAAAAAAAAAA A G SOX4 Ensembl:ENSG00000124766 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:21594058..21594240 26863196 MeRIP-seq:(Medium) rs1234272534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1394571,Human_RBP_ID_1668428,Human_RBP_ID_2016342,Human_RBP_ID_4875147,Human_RBP_ID_8898874,Human_RBP_ID_18070868,Human_RBP_ID_18860153,Human_RBP_ID_23068640,Human_RBP_ID_27093313 Human_miRNA_ID_1004959 68578 RMVar_ID_68578 Human_SNP_ID_269534180 m1A Human chr6 - 21594254 21594254 21594254 TCTCCCTCTCTCTCGCTCTCTCACCGCGCTGCAGTTTGCTGTCTCTCGGCTGAGTCTGGAGACCG TCTCCCTCTCTCTCGCTCTCTCACCGCGCTGCGGTTTGCTGTCTCTCGGCTGAGTCTGGAGACCG T C AL512380.2 Ensembl:ENSG00000283480 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:21594205..21594779 26863196 MeRIP-seq:(Medium) rs1046242085 Functional Loss SNV dbSNP153 33..33 33 - - - 68579 RMVar_ID_68579 Human_SNP_ID_269534186 m1A Human chr6 + 21594284 21594272 21594284 ACTGCAGCGCGGTGAGAGAGCGAGAGAGAGGGAGAGAGAGACTCTCCAGCCTGGGAACTATAACT ACTGCAGCGCGGTGAGAGAGC____________GAGAGAGACTCTCCAGCCTGGGAACTATAACT CGAGAGAGAGGGA C SOX4 Ensembl:ENSG00000124766 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21594102..21594425 26863196 MeRIP-seq:(Medium) rs986447437 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_3803595,Human_RBP_ID_4875158,Human_RBP_ID_7583227 68580 RMVar_ID_68580 Human_SNP_ID_269534200 m1A Human chr6 + 21594284 21594284 21594284 ACTGCAGCGCGGTGAGAGAGCGAGAGAGAGGGAGAGAGAGACTCTCCAGCCTGGGAACTATAACT ACTGCAGCGCGGTGAGAGAGCGAGAGAGAGGGGGAGAGAGACTCTCCAGCCTGGGAACTATAACT A G SOX4 Ensembl:ENSG00000124766 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21594102..21594425 26863196 MeRIP-seq:(Medium) rs941841472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3803595,Human_RBP_ID_4875158,Human_RBP_ID_7583227 68581 RMVar_ID_68581 Human_SNP_ID_269534477 m1A Human chr6 - 21594976 21594973 21594976 GACCTTGTCTCCCTTCTCCCCCGGCTTGGAGGAGGCGGCGGCCGAGGAGCTGGAGTTGGCGTTGC GACCTTGTCTCCCTTCTCCCCCGGCTTGGAGG___CGGCGGCCGAGGAGCTGGAGTTGGCGTTGC GCCT G AL512380.2 Ensembl:ENSG00000283480 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:21594931..21595124 26863196 MeRIP-seq:(Medium) rs1346225479 Functional Loss DEL dbSNP153 33..35 33 - - - 68582 RMVar_ID_68582 Human_SNP_ID_269534478 m1A Human chr6 - 21594976 21594976 21594976 GACCTTGTCTCCCTTCTCCCCCGGCTTGGAGGAGGCGGCGGCCGAGGAGCTGGAGTTGGCGTTGC GACCTTGTCTCCCTTCTCCCCCGGCTTGGAGGCGGCGGCGGCCGAGGAGCTGGAGTTGGCGTTGC T G AL512380.2 Ensembl:ENSG00000283480 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:21594931..21595124 26863196 MeRIP-seq:(Medium) rs753643945 Functional Loss SNV dbSNP153 33..33 33 - - - 68583 RMVar_ID_68583 Human_SNP_ID_269534504 m1A Human chr6 + 21595031 21595020 21595032 AGACAAGGTCGGTGGCAGTGGCGGGGGCGGCCATGGGGGCGGCGGCGGCGGCGGGAGCAGCAACG AGACAAGGTCGGTGGCAGTGGC____________GGGGGCGGCGGCGGCGGCGGGAGCAGCAACG CGGGGGCGGCCAT C SOX4 Ensembl:ENSG00000124766 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:21594487..21595150 26863196 MeRIP-seq:(Medium) rs747523746 Functional Loss DEL dbSNP153,HGVD 23..34 33 - - - Human_RBP_ID_4909482,Human_RBP_ID_22728133 68584 RMVar_ID_68584 Human_SNP_ID_269534728 m1A Human chr6 + 21595371 21595371 21595371 GCCTCCGCCTCCTCGGCAGCCTCGGCCTCCGCAGCGCTCGCGGCCCCGGGCAAGCACCTGGCGGA GCCTCCGCCTCCTCGGCAGCCTCGGCCTCCGCCGCGCTCGCGGCCCCGGGCAAGCACCTGGCGGA A C SOX4 Ensembl:ENSG00000124766 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:21595276..21595425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22461613 68585 RMVar_ID_68585 Human_SNP_ID_269534782 m1A Human chr6 - 21595453 21595453 21595453 GTCGGCTCCCGCGCCCACGCCGCCCACGGGCGACGACGACGTGCCCAGGCCGCCGAACAGGTAGA GTCGGCTCCCGCGCCCACGCCGCCCACGGGCGGCGACGACGTGCCCAGGCCGCCGAACAGGTAGA T C AL512380.2 Ensembl:ENSG00000283480 lincRNA exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr6:21595402..21595750;chr6:21595270..21595752 26863196 MeRIP-seq:(Medium) rs765502866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_741805 68586 RMVar_ID_68586 Human_SNP_ID_269534783 m1A Human chr6 - 21595453 21595453 21595453 GTCGGCTCCCGCGCCCACGCCGCCCACGGGCGACGACGACGTGCCCAGGCCGCCGAACAGGTAGA GTCGGCTCCCGCGCCCACGCCGCCCACGGGCGCCGACGACGTGCCCAGGCCGCCGAACAGGTAGA T G AL512380.2 Ensembl:ENSG00000283480 lincRNA exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr6:21595402..21595750;chr6:21595270..21595752 26863196 MeRIP-seq:(Medium) rs765502866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_741805 68587 RMVar_ID_68587 Human_SNP_ID_269534816 m1A Human chr6 + 21595511 21595511 21595511 AGCCGACCCCAGCGACCCCCTGGGCCTGTACGAGGAGGAGGGCGCGGGCTGCTCGCCCGACGCGC AGCCGACCCCAGCGACCCCCTGGGCCTGTACGGGGAGGAGGGCGCGGGCTGCTCGCCCGACGCGC A G SOX4 Ensembl:ENSG00000124766 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:21595412..21595710 26863196 MeRIP-seq:(Medium) rs1375401399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7583250,Human_RBP_ID_22460931,Human_RBP_ID_27521651 68588 RMVar_ID_68588 Human_SNP_ID_269534870 m1A Human chr6 + 21595616 21595616 21595616 CGCCGGCCGCTCGCCCGCCGACCACCGCGGCTACGCCAGCCTGCGCGCCGCCTCGCCCGCCCCGT CGCCGGCCGCTCGCCCGCCGACCACCGCGGCTGCGCCAGCCTGCGCGCCGCCTCGCCCGCCCCGT A G SOX4 Ensembl:ENSG00000124766 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr6:21595426..21595700;chr6:21595544..21595693 26863410 MeRIP-seq:(Medium) rs1384081551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4909492 68589 RMVar_ID_68589 Human_SNP_ID_269535129 m1A Human chr6 + 21596023 21596020 21596024 GGGTAGGAGAGGAGAAAAAAAAAGTGAAAAAAAGAAACGAAAAGGACAGACGAAGAGTTTAAAGA GGGTAGGAGAGGAGAAAAAAAAAGTGAAAA____AAACGAAAAGGACAGACGAAGAGTTTAAAGA AAAAG A SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21595901..21596165 26863196 MeRIP-seq:(Medium) rs1025265961 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_1668455,Human_RBP_ID_2016353,Human_RBP_ID_3803598,Human_RBP_ID_8639560 68590 RMVar_ID_68590 Human_SNP_ID_269535131 m1A Human chr6 + 21596023 21596022 21596024 GGGTAGGAGAGGAGAAAAAAAAAGTGAAAAAAAGAAACGAAAAGGACAGACGAAGAGTTTAAAGA GGGTAGGAGAGGAGAAAAAAAAAGTGAAAAAA__AAACGAAAAGGACAGACGAAGAGTTTAAAGA AAG A SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21595901..21596165 26863196 MeRIP-seq:(Medium) rs1203175941 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1668455,Human_RBP_ID_2016353,Human_RBP_ID_3803598,Human_RBP_ID_8639560 68591 RMVar_ID_68591 Human_SNP_ID_269535133 m1A Human chr6 + 21596025 21596025 21596025 GTAGGAGAGGAGAAAAAAAAAGTGAAAAAAAGAAACGAAAAGGACAGACGAAGAGTTTAAAGAGA GTAGGAGAGGAGAAAAAAAAAGTGAAAAAAAGCAACGAAAAGGACAGACGAAGAGTTTAAAGAGA A C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:21595976..21596113;chr6:21595950..21596157 26863196 MeRIP-seq:(Medium) rs546528035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1668455,Human_RBP_ID_2016353,Human_RBP_ID_3803598,Human_RBP_ID_8639560 68592 RMVar_ID_68592 Human_SNP_ID_269535244 m1A Human chr6 + 21596272 21596269 21596273 ATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT ATTGTTGTTATTGATGTTGTTGTTGATGGC____AAAAAAAAGCGACTTCGAGTTTGCTCCCCTT CAAAA C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596221..21596370 26863196 MeRIP-seq:(Medium) rs796555280 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 68593 RMVar_ID_68593 Human_SNP_ID_269535245 m1A Human chr6 + 21596272 21596269 21596273 ATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT ATTGTTGTTATTGATGTTGTTGTTGATGGCA___AAAAAAAAGCGACTTCGAGTTTGCTCCCCTT CAAAA CA SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596221..21596370 26863196 MeRIP-seq:(Medium) rs796555280 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 68594 RMVar_ID_68594 Human_SNP_ID_269535246 m1A Human chr6 + 21596272 21596269 21596273 ATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT ATTGTTGTTATTGATGTTGTTGTTGATGGCAA__AAAAAAAAGCGACTTCGAGTTTGCTCCCCTT CAAAA CAA SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596221..21596370 26863196 MeRIP-seq:(Medium) rs796555280 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 68595 RMVar_ID_68595 Human_SNP_ID_269535250 m1A Human chr6 + 21596271 21596271 21596271 GATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCT GATTGTTGTTATTGATGTTGTTGTTGATGGCACAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCT A C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21596220..21596315 26863196 MeRIP-seq:(Medium) rs1175419487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 68596 RMVar_ID_68596 Human_SNP_ID_269535393 m1A Human chr6 - 21596574 21596573 21596575 CCAAACGGGAATTCGCCTGCGTGGAGTCTCTCAGTCCCGGCGTTCCCCCAAAACATCTGCCATCG CCAAACGGGAATTCGCCTGCGTGGAGTCTCT__GTCCCGGCGTTCCCCCAAAACATCTGCCATCG CTG C RF00017-4503,lnc-PRL-13 RNACentral:URS0000948B80,RNACentral:URS0000D5CEDC SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596523..21596607 26863196 MeRIP-seq:(Medium) rs1212027588 Functional Loss DEL dbSNP153 32..33 33 - - - 68597 RMVar_ID_68597 Human_SNP_ID_269535395 m1A Human chr6 - 21596574 21596574 21596574 CCAAACGGGAATTCGCCTGCGTGGAGTCTCTCAGTCCCGGCGTTCCCCCAAAACATCTGCCATCG CCAAACGGGAATTCGCCTGCGTGGAGTCTCTCGGTCCCGGCGTTCCCCCAAAACATCTGCCATCG T C RF00017-4503,lnc-PRL-13 RNACentral:URS0000948B80,RNACentral:URS0000D5CEDC SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596523..21596607 26863196 MeRIP-seq:(Medium) rs1445190920 Functional Loss SNV dbSNP153 33..33 33 - - - 68598 RMVar_ID_68598 Human_SNP_ID_270264331 m1A Human chr6 + 24403001 24403001 24403001 CAGAGCTGCGGCCTGAGCAGCCAGCGTCCGGCATGAAGGTCTGGGGTCTGGCTGCTGCCTGCTTC CAGAGCTGCGGCCTGAGCAGCCAGCGTCCGGCGTGAAGGTCTGGGGTCTGGCTGCTGCCTGCTTC A G MRS2 Ensembl:ENSG00000124532 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24402951..24403125 26863196 MeRIP-seq:(Medium) rs753382333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4875418,Human_RBP_ID_5477705,Human_RBP_ID_5510973,Human_RBP_ID_18425367,Human_RBP_ID_22618028,Human_RBP_ID_24152456 68599 RMVar_ID_68599 Human_SNP_ID_270264332 m1A Human chr6 + 24403001 24403001 24403001 CAGAGCTGCGGCCTGAGCAGCCAGCGTCCGGCATGAAGGTCTGGGGTCTGGCTGCTGCCTGCTTC CAGAGCTGCGGCCTGAGCAGCCAGCGTCCGGCTTGAAGGTCTGGGGTCTGGCTGCTGCCTGCTTC A T MRS2 Ensembl:ENSG00000124532 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24402951..24403125 26863196 MeRIP-seq:(Medium) rs753382333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4875418,Human_RBP_ID_5477705,Human_RBP_ID_5510973,Human_RBP_ID_18425367,Human_RBP_ID_22618028,Human_RBP_ID_24152456 68600 RMVar_ID_68600 Human_SNP_ID_270264333 m1A Human chr6 - 24403002 24403002 24403002 AGAAGCAGGCAGCAGCCAGACCCCAGACCTTCATGCCGGACGCTGGCTGCTCAGGCCGCAGCTCT AGAAGCAGGCAGCAGCCAGACCCCAGACCTTCCTGCCGGACGCTGGCTGCTCAGGCCGCAGCTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:24402951..24403073 26863196 MeRIP-seq:(Medium) rs1317791822 Functional Loss SNV dbSNP153 33..33 33 - - - 68601 RMVar_ID_68601 Human_SNP_ID_270267093 m1A Human chr6 + 24413231 24413230 24413231 CTCTCAGGAGCTCATGCTGTTAGGAGAAAGACAGGGATCTTAAAGGGAGCAGGAGGGGAAGGAGA CTCTCAGGAGCTCATGCTGTTAGGAGAAAGAC_GGGATCTTAAAGGGAGCAGGAGGGGAAGGAGA CA C MRS2 Ensembl:ENSG00000124532 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:24413183..24413366 26863196 MeRIP-seq:(Medium) rs1385011261 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3000399,Human_RBP_ID_15766104 RMVar_hsa_circ_18815,RMVar_hsa_circ_50579,RMVar_hsa_circ_286889,RMVar_hsa_circ_47250,RMVar_hsa_circ_237601,RMVar_hsa_circ_360872,RMVar_hsa_circ_22930,RMVar_hsa_circ_335616,RMVar_hsa_circ_55878,RMVar_hsa_circ_55377,RMVar_hsa_circ_285996,RMVar_hsa_circ_237602 68602 RMVar_ID_68602 Human_SNP_ID_270267094 m1A Human chr6 + 24413231 24413231 24413231 CTCTCAGGAGCTCATGCTGTTAGGAGAAAGACAGGGATCTTAAAGGGAGCAGGAGGGGAAGGAGA CTCTCAGGAGCTCATGCTGTTAGGAGAAAGACGGGGATCTTAAAGGGAGCAGGAGGGGAAGGAGA A G MRS2 Ensembl:ENSG00000124532 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:24413183..24413366 26863196 MeRIP-seq:(Medium) rs1364825724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3000399,Human_RBP_ID_15766104 RMVar_hsa_circ_18815,RMVar_hsa_circ_50579,RMVar_hsa_circ_286889,RMVar_hsa_circ_47250,RMVar_hsa_circ_237601,RMVar_hsa_circ_360872,RMVar_hsa_circ_22930,RMVar_hsa_circ_335616,RMVar_hsa_circ_55878,RMVar_hsa_circ_55377,RMVar_hsa_circ_285996,RMVar_hsa_circ_237602 68603 RMVar_ID_68603 Human_SNP_ID_270269283 m1A Human chr6 + 24420801 24420801 24420801 ACAGAAGTAAAGATTGAGGCAGGAACGATCTGAGCTTGTTCATGAAATGGCAAGAAGGTTGGAAT ACAGAAGTAAAGATTGAGGCAGGAACGATCTGGGCTTGTTCATGAAATGGCAAGAAGGTTGGAAT A G MRS2 Ensembl:ENSG00000124532 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:24420753..24420839 26863196 MeRIP-seq:(Medium) rs1011999019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15766213,Human_RBP_ID_24152479 RMVar_hsa_circ_77903,RMVar_hsa_circ_237604 68604 RMVar_ID_68604 Human_SNP_ID_270290440 m1A Human chr6 - 24494975 24494975 24494975 CAGGTCGCCATGGCCCGGGCAACGACGGCGACAGGAAACAGGCAAGCGGGCGCGCGCGCACGGGA CAGGTCGCCATGGCCCGGGCAACGACGGCGACGGGAAACAGGCAAGCGGGCGCGCGCGCACGGGA T C GPLD1 Ensembl:ENSG00000112293 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:24494890..24495012 26863196 MeRIP-seq:(Medium) rs750617560 Functional Loss SNV dbSNP153 33..33 33 - - - 68605 RMVar_ID_68605 Human_SNP_ID_270290452 m1A Human chr6 - 24494998 24494998 24494998 CCCCACAGCTCCGCAGCCAAATGCAGGTCGCCATGGCCCGGGCAACGACGGCGACAGGAAACAGG CCCCACAGCTCCGCAGCCAAATGCAGGTCGCCGTGGCCCGGGCAACGACGGCGACAGGAAACAGG T C GPLD1 Ensembl:ENSG00000112293 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:24494901..24495001 26863410 MeRIP-seq:(Medium) rs1248373329 Functional Loss SNV dbSNP153 33..33 33 - - - 68606 RMVar_ID_68606 Human_SNP_ID_270296386 m1A Human chr6 + 24518343 24518343 24518343 AGATTCATTAAGACATGACAGGAGTTTACACTATACCCAGTGGCCAGGGCAAGCCGCCTTCCTGG AGATTCATTAAGACATGACAGGAGTTTACACTGTACCCAGTGGCCAGGGCAAGCCGCCTTCCTGG A G ALDH5A1 Ensembl:ENSG00000112294 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:24518334..24518442 26863196 MeRIP-seq:(Medium) rs1334596552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237624,RMVar_hsa_circ_279775,RMVar_hsa_circ_296458,RMVar_hsa_circ_237625,RMVar_hsa_circ_328533,RMVar_hsa_circ_355558 68607 RMVar_ID_68607 Human_SNP_ID_270332085 m1A Human chr6 - 24666602 24666602 24666602 TCCCTTGTGCCTTTGTTTTTCAGAGGGCTCTGAACTCCTACTTCGAGCCTCCGGTGGAGGAGAGC TCCCTTGTGCCTTTGTTTTTCAGAGGGCTCTGGACTCCTACTTCGAGCCTCCGGTGGAGGAGAGC T C TDP2 Ensembl:ENSG00000111802 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:24666551..24666625 32194978 MeRIP-seq:(Medium) rs35744230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949102,Human_RBP_ID_22553533,Human_RBP_ID_24152615 Human_Splice_Rec_743664,Human_Splice_Rec_743665,Human_Splice_Rec_743676,Human_Splice_Rec_743677,Human_Splice_Rec_743686 RMVar_hsa_circ_100061,RMVar_hsa_circ_322919,RMVar_hsa_circ_237646,RMVar_hsa_circ_65904 68608 RMVar_ID_68608 Human_SNP_ID_270332401 m1A Human chr6 - 24667116 24667116 24667116 TCCGCCCCTAGGAGCGCAAGAGGCCGGGAGTCAGGCGAGCTGGCAGCCCCGGTGGTCCGCGATTT TCCGCCCCTAGGAGCGCAAGAGGCCGGGAGTCGGGCGAGCTGGCAGCCCCGGTGGTCCGCGATTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24667051..24667374 26863196 MeRIP-seq:(Medium) rs1263555842 Functional Loss SNV dbSNP153 33..33 33 - - - 68609 RMVar_ID_68609 Human_SNP_ID_270339893 m1A Human chr6 - 24698001 24698001 24698001 CCCTTTCCGTGCATAGCAGAGCCATTGTTGATATGTTATCTACTAACGTGGCTGTCAAACCGCCG CCCTTTCCGTGCATAGCAGAGCCATTGTTGATCTGTTATCTACTAACGTGGCTGTCAAACCGCCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:24697951..24698050 26863196 MeRIP-seq:(Medium) rs1012817519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1668544 68610 RMVar_ID_68610 Human_SNP_ID_270340927 m1A Human chr6 - 24701575 24701571 24701575 CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATTAATTTTCCTGTGGCCTTGTTGGTCAGATCCACA CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATT____TTCCTGTGGCCTTGTTGGTCAGATCCACA AAATT A AL031775.1 Ensembl:ENSG00000272345 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24701525..24701605 26863196 MeRIP-seq:(Medium) rs746562084 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3000481,Human_RBP_ID_3803848 68611 RMVar_ID_68611 Human_SNP_ID_270346287 m1A Human chr6 + 24719691 24719691 24719691 TCCTACATTCCCCAAGGGAGACTTCCCTGTGGATCTGCCCCCGTTCAAAATGGTGGGGAGTGCGA TCCTACATTCCCCAAGGGAGACTTCCCTGTGGCTCTGCCCCCGTTCAAAATGGTGGGGAGTGCGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr6:24719640..24719852;chr6:24719650..24719807;chr6:24719640..24719741 26863196,32194978 MeRIP-seq:(Medium) rs1046940060 Functional Loss SNV dbSNP153 33..33 33 - - - 68612 RMVar_ID_68612 Human_SNP_ID_270346534 m1A Human chr6 - 24720122 24720122 24720122 GCTGCCTCAATTCCACCCCCTGCCCCTCGGGAAACAACTAACGACCCCACCCTAAACAATCCAAA GCTGCCTCAATTCCACCCCCTGCCCCTCGGGAGACAACTAACGACCCCACCCTAAACAATCCAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24720076..24720607 26863196 MeRIP-seq:(Medium) rs1436986784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658871,Human_RBP_ID_4909687,Human_RBP_ID_5090283,Human_RBP_ID_7584657,Human_RBP_ID_8269801,Human_RBP_ID_15767773,Human_RBP_ID_17091100,Human_RBP_ID_17419170,Human_RBP_ID_18957129,Human_RBP_ID_21947701,Human_RBP_ID_22830256,Human_RBP_ID_24562611,Human_RBP_ID_26534279,Human_RBP_ID_27842370 68613 RMVar_ID_68613 Human_SNP_ID_270346535 m1A Human chr6 - 24720122 24720122 24720122 GCTGCCTCAATTCCACCCCCTGCCCCTCGGGAAACAACTAACGACCCCACCCTAAACAATCCAAA GCTGCCTCAATTCCACCCCCTGCCCCTCGGGACACAACTAACGACCCCACCCTAAACAATCCAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24720076..24720607 26863196 MeRIP-seq:(Medium) rs1436986784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658871,Human_RBP_ID_4909687,Human_RBP_ID_5090283,Human_RBP_ID_7584657,Human_RBP_ID_8269801,Human_RBP_ID_15767773,Human_RBP_ID_17091100,Human_RBP_ID_17419170,Human_RBP_ID_18957129,Human_RBP_ID_21947701,Human_RBP_ID_22830256,Human_RBP_ID_24562611,Human_RBP_ID_26534279,Human_RBP_ID_27842370 68614 RMVar_ID_68614 Human_SNP_ID_270346660 m1A Human chr6 - 24720374 24720374 24720374 AGCGCGGGCGGTCCAGTCACGGTGCGCACTGCAGCGGGGATGGAGGGGCTCAGTTGGCTGGTGGT AGCGCGGGCGGTCCAGTCACGGTGCGCACTGCTGCGGGGATGGAGGGGCTCAGTTGGCTGGTGGT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:24720326..24720375 26863196 MeRIP-seq:(Medium) rs1336797436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4909694,Human_RBP_ID_5477716,Human_RBP_ID_7584661,Human_RBP_ID_15767785,Human_RBP_ID_18449913,Human_RBP_ID_24562743 68615 RMVar_ID_68615 Human_SNP_ID_270346739 m1A Human chr6 - 24720550 24720550 24720550 TCCTTTCCCTTCCCCCTCCGCCGCCAGTACCAATCCAACTCCCCATCTTTCTCTTTGTTTTTCCT TCCTTTCCCTTCCCCCTCCGCCGCCAGTACCAGTCCAACTCCCCATCTTTCTCTTTGTTTTTCCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:24720501..24720550 26863196 MeRIP-seq:(Medium) rs944673049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658872,Human_RBP_ID_3803898,Human_RBP_ID_4903721,Human_RBP_ID_5428150,Human_RBP_ID_5450839,Human_RBP_ID_5477722,Human_RBP_ID_5510991,Human_RBP_ID_7584672,Human_RBP_ID_8140973,Human_RBP_ID_9192709,Human_RBP_ID_18071157,Human_RBP_ID_18957131,Human_RBP_ID_23058946,Human_RBP_ID_24152746,Human_RBP_ID_27343866,Human_RBP_ID_27521780 68616 RMVar_ID_68616 Human_SNP_ID_270346875 m1A Human chr6 + 24720796 24720796 24720796 CCCCCCCCCGCCGGTGGCTGCAGAAGCGGCGAAGGCCTCGGGCGCCTCGCGGGTCCGGGGCAGAG CCCCCCCCCGCCGGTGGCTGCAGAAGCGGCGACGGCCTCGGGCGCCTCGCGGGTCCGGGGCAGAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr6:24720721..24720809;chr6:24720076..24720850 26863410,26863196 MeRIP-seq:(Medium) rs3813686 Functional Loss SNV dbSNP153 33..33 33 - - - 68617 RMVar_ID_68617 Human_SNP_ID_270361803 m1A Human chr6 + 24781573 24781573 24781573 CTGGGGTTATTGTCCCAGAATCTAGTGAAAATAAAAATCTTGGAGGAGTCACCCAGGAGTCATTT CTGGGGTTATTGTCCCAGAATCTAGTGAAAATGAAAATCTTGGAGGAGTCACCCAGGAGTCATTT A G GMNN Ensembl:ENSG00000112312 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:24781534..24784098 32194978 MeRIP-seq:(Medium) rs370562633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841980,Human_RBP_ID_948052,Human_RBP_ID_1668695,Human_RBP_ID_2016587,Human_RBP_ID_4875856,Human_RBP_ID_8639806,Human_RBP_ID_9400040,Human_RBP_ID_18071180,Human_RBP_ID_23058978,Human_RBP_ID_26353453,Human_RBP_ID_27093571,Human_RBP_ID_27827363 Human_Splice_Rec_743736,Human_Splice_Rec_743737,Human_Splice_Rec_743748,Human_Splice_Rec_743749,Human_Splice_Rec_743762,Human_Splice_Rec_743763,Human_Splice_Rec_743774,Human_Splice_Rec_743775,Human_Splice_Rec_743786,Human_Splice_Rec_743790,Human_Splice_Rec_743791 RMVar_hsa_circ_111992,RMVar_hsa_circ_354607,RMVar_hsa_circ_299181,RMVar_hsa_circ_237652 68618 RMVar_ID_68618 Human_SNP_ID_270476050 m1A Human chr6 + 25279496 25279496 25279496 ACCAGCGAGCCGGGAGGAGGAGCAGGCGCCACAGCCGCCCCGCGCCCCGCGCCCGCTTGTAATCC ACCAGCGAGCCGGGAGGAGGAGCAGGCGCCACCGCCGCCCCGCGCCCCGCGCCCGCTTGTAATCC A C CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:25279454..25279572 26863196 MeRIP-seq:(Medium) rs1362633295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658903,Human_RBP_ID_4909741 RMVar_hsa_circ_91415,RMVar_hsa_circ_237666 68619 RMVar_ID_68619 Human_SNP_ID_270507459 m1A Human chr6 + 25416015 25416015 25416015 AGGAGGGGTGGGGAGCCAGTGAGGAGAGGCACAGATAGACTGAGAGGTACATACGTAGAATCATG AGGAGGGGTGGGGAGCCAGTGAGGAGAGGCACGGATAGACTGAGAGGTACATACGTAGAATCATG A G CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:25416000..25416086 26863196 MeRIP-seq:(Medium) rs1276741870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2072,RMVar_hsa_circ_74567,RMVar_hsa_circ_91415,RMVar_hsa_circ_237666,RMVar_hsa_circ_60670 68620 RMVar_ID_68620 Human_SNP_ID_270512711 m1A Human chr6 - 25440295 25440295 25440295 CTCTCTCCTCTGAATTTTCTCCATCCGTTTGCAGTAAATCTCCTCTGCAAAGCCAGCCTGTGCTC CTCTCTCCTCTGAATTTTCTCCATCCGTTTGCTGTAAATCTCCTCTGCAAAGCCAGCCTGTGCTC T A CMAHP Ensembl:ENSG00000168405 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:25440259..25440369 26863196 MeRIP-seq:(Medium) rs562634506 Functional Loss SNV dbSNP153 33..33 33 - - - 68621 RMVar_ID_68621 Human_SNP_ID_270512712 m1A Human chr6 - 25440295 25440295 25440295 CTCTCTCCTCTGAATTTTCTCCATCCGTTTGCAGTAAATCTCCTCTGCAAAGCCAGCCTGTGCTC CTCTCTCCTCTGAATTTTCTCCATCCGTTTGCGGTAAATCTCCTCTGCAAAGCCAGCCTGTGCTC T C CMAHP Ensembl:ENSG00000168405 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:25440259..25440369 26863196 MeRIP-seq:(Medium) rs562634506 Functional Loss SNV dbSNP153 33..33 33 - - - 68622 RMVar_ID_68622 Human_SNP_ID_270548113 m1A Human chr6 + 25600614 25600614 25600614 GACTCCTTTGAAGAGAGTCAAGGGGAAGAAATAGGGAAGGTGGAACGGAGTGACAGCAAGAGCAG GACTCCTTTGAAGAGAGTCAAGGGGAAGAAATGGGGAAGGTGGAACGGAGTGACAGCAAGAGCAG A G CARMIL1 Ensembl:ENSG00000079691 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:25600564..25600750 26863196 MeRIP-seq:(Medium) rs1393989163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2996104 RMVar_hsa_circ_29101,RMVar_hsa_circ_8251,RMVar_hsa_circ_25613,RMVar_hsa_circ_63427,RMVar_hsa_circ_86533,RMVar_hsa_circ_23461,RMVar_hsa_circ_52099,RMVar_hsa_circ_123442,RMVar_hsa_circ_237718,RMVar_hsa_circ_237719,RMVar_hsa_circ_25031,RMVar_hsa_circ_23244,RMVar_hsa_circ_237725,RMVar_hsa_circ_47395,RMVar_hsa_circ_74455,RMVar_hsa_circ_17771,RMVar_hsa_circ_356312,RMVar_hsa_circ_237727,RMVar_hsa_circ_364624 68623 RMVar_ID_68623 Human_SNP_ID_270644829 m1A Human chr6 - 26021710 26021690 26021711 CCTTGCGGTGGCGCTTGGCACCCCCCTTACCCAAACCCTTCCCGCCCTTACCACGTCCAGACATG CCTTGCGGTGGCGCTTGGCACCCCCCTTACC_____________________ACGTCCAGACATG TGGTAAGGGCGGGAAGGGTTTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26021651..26021850 26863196 MeRIP-seq:(Medium) rs1194851882 Functional Loss DEL dbSNP153 32..52 33 - - - 68624 RMVar_ID_68624 Human_SNP_ID_270644845 m1A Human chr6 + 26021716 26021716 26021716 TGGACGTGGTAAGGGCGGGAAGGGTTTGGGTAAGGGGGGTGCCAAGCGCCACCGCAAGGTGTTGC TGGACGTGGTAAGGGCGGGAAGGGTTTGGGTAGGGGGGGTGCCAAGCGCCACCGCAAGGTGTTGC A G H4C1 Ensembl:ENSG00000278637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:26021648..26021875;chr6:26021597..26021825;chr6:26021617..26021782 26863196 MeRIP-seq:(Medium) rs1561915123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658927,Human_RBP_ID_791642,Human_RBP_ID_4876009,Human_RBP_ID_5327063,Human_RBP_ID_5478656,Human_RBP_ID_7585510,Human_RBP_ID_8237087,Human_RBP_ID_9335976,Human_RBP_ID_15769935,Human_RBP_ID_18071276,Human_RBP_ID_22426604,Human_RBP_ID_22460417,Human_RBP_ID_22482509,Human_RBP_ID_22618044,Human_RBP_ID_22706035,Human_RBP_ID_22830295,Human_RBP_ID_23214657,Human_RBP_ID_24153167,Human_RBP_ID_27093604,Human_RBP_ID_27343905,Human_RBP_ID_27842371 68625 RMVar_ID_68625 Human_SNP_ID_270646652 m1A Human chr6 - 26027150 26027150 26027150 GGGATAACATCCAAGGCATCACCAAACCGGCCATTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG GGGATAACATCCAAGGCATCACCAAACCGGCCTTTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG T A H4C2 Ensembl:ENSG00000278705 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26027100..26027275 26863196 MeRIP-seq:(Medium) rs778075262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284845,Human_RBP_ID_1045953,Human_RBP_ID_1216555,Human_RBP_ID_1668784,Human_RBP_ID_2016650,Human_RBP_ID_3804118,Human_RBP_ID_4876023,Human_RBP_ID_5268317,Human_RBP_ID_5428169,Human_RBP_ID_5511018,Human_RBP_ID_9336480,Human_RBP_ID_9354682,Human_RBP_ID_17305943,Human_RBP_ID_18071287,Human_RBP_ID_22460419,Human_RBP_ID_27093611,Human_RBP_ID_27343917,Human_RBP_ID_27521818,Human_RBP_ID_27568174,Human_RBP_ID_27842372 68626 RMVar_ID_68626 Human_SNP_ID_270646653 m1A Human chr6 - 26027150 26027150 26027150 GGGATAACATCCAAGGCATCACCAAACCGGCCATTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG GGGATAACATCCAAGGCATCACCAAACCGGCCGTTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG T C H4C2 Ensembl:ENSG00000278705 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26027100..26027275 26863196 MeRIP-seq:(Medium) rs778075262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284845,Human_RBP_ID_1045953,Human_RBP_ID_1216555,Human_RBP_ID_1668784,Human_RBP_ID_2016650,Human_RBP_ID_3804118,Human_RBP_ID_4876023,Human_RBP_ID_5268317,Human_RBP_ID_5428169,Human_RBP_ID_5511018,Human_RBP_ID_9336480,Human_RBP_ID_9354682,Human_RBP_ID_17305943,Human_RBP_ID_18071287,Human_RBP_ID_22460419,Human_RBP_ID_27093611,Human_RBP_ID_27343917,Human_RBP_ID_27521818,Human_RBP_ID_27568174,Human_RBP_ID_27842372 68627 RMVar_ID_68627 Human_SNP_ID_270646654 m1A Human chr6 - 26027150 26027150 26027150 GGGATAACATCCAAGGCATCACCAAACCGGCCATTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG GGGATAACATCCAAGGCATCACCAAACCGGCCCTTCGGCGCCTTGCTAGGCGTGGTGGGGTTAAG T G H4C2 Ensembl:ENSG00000278705 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26027100..26027275 26863196 MeRIP-seq:(Medium) rs778075262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284845,Human_RBP_ID_1045953,Human_RBP_ID_1216555,Human_RBP_ID_1668784,Human_RBP_ID_2016650,Human_RBP_ID_3804118,Human_RBP_ID_4876023,Human_RBP_ID_5268317,Human_RBP_ID_5428169,Human_RBP_ID_5511018,Human_RBP_ID_9336480,Human_RBP_ID_9354682,Human_RBP_ID_17305943,Human_RBP_ID_18071287,Human_RBP_ID_22460419,Human_RBP_ID_27093611,Human_RBP_ID_27343917,Human_RBP_ID_27521818,Human_RBP_ID_27568174,Human_RBP_ID_27842372 68628 RMVar_ID_68628 Human_SNP_ID_270646738 m1A Human chr6 + 26027221 26027221 26027221 CTTTTCGGTGACGCTTGGCACCTCCCTTACCCAAACCTTTACCGCCTTTGCCGCGACCAGACATG CTTTTCGGTGACGCTTGGCACCTCCCTTACCCCAACCTTTACCGCCTTTGCCGCGACCAGACATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26027129..26027275 26863196 MeRIP-seq:(Medium) rs757142938 Functional Loss SNV dbSNP153 33..33 33 - - - 68629 RMVar_ID_68629 Human_SNP_ID_270646744 m1A Human chr6 - 26027228 26027228 26027228 GGTTAGACATGTCTGGTCGCGGCAAAGGCGGTAAAGGTTTGGGTAAGGGAGGTGCCAAGCGTCAC GGTTAGACATGTCTGGTCGCGGCAAAGGCGGTGAAGGTTTGGGTAAGGGAGGTGCCAAGCGTCAC T C H4C2 Ensembl:ENSG00000278705 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26027226..26027275 26863196 MeRIP-seq:(Medium) rs750679477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658938,Human_RBP_ID_792081,Human_RBP_ID_1045955,Human_RBP_ID_1142365,Human_RBP_ID_1326420,Human_RBP_ID_1394666,Human_RBP_ID_1668785,Human_RBP_ID_2016650,Human_RBP_ID_4876024,Human_RBP_ID_5511019,Human_RBP_ID_8639942,Human_RBP_ID_9192796,Human_RBP_ID_9336480,Human_RBP_ID_9354682,Human_RBP_ID_15769952,Human_RBP_ID_18071289,Human_RBP_ID_21314923,Human_RBP_ID_22534137,Human_RBP_ID_23137881,Human_RBP_ID_23214661,Human_RBP_ID_24153184,Human_RBP_ID_26534316,Human_RBP_ID_27093613,Human_RBP_ID_27343919,Human_RBP_ID_27842375 68630 RMVar_ID_68630 Human_SNP_ID_270646787 m1A Human chr6 + 26027251 26027251 26027251 CCAAACCTTTACCGCCTTTGCCGCGACCAGACATGTCTAACCAGCTGACAACAAAAACCAGGTAC CCAAACCTTTACCGCCTTTGCCGCGACCAGACGTGTCTAACCAGCTGACAACAAAAACCAGGTAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26027201..26027275 26863196 MeRIP-seq:(Medium) rs150979745 Functional Loss SNV dbSNP153 33..33 33 - - - 68631 RMVar_ID_68631 Human_SNP_ID_270648363 m1A Human chr6 - 26031950 26031950 26031950 CGCAAGAGCGCGCCGGCTACCGGCGGCGTGAAAAAGCCTCACCGTTACCGCCCGGGCACTGTGGC CGCAAGAGCGCGCCGGCTACCGGCGGCGTGAAGAAGCCTCACCGTTACCGCCCGGGCACTGTGGC T C H3C2 Ensembl:ENSG00000286522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26031907..26032100 26863196 MeRIP-seq:(Medium) rs1223521176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172989,Human_RBP_ID_1045964,Human_RBP_ID_1668789,Human_RBP_ID_4909808,Human_RBP_ID_5477739,Human_RBP_ID_8899059,Human_RBP_ID_15769973,Human_RBP_ID_18860517 68632 RMVar_ID_68632 Human_SNP_ID_270656281 m1A Human chr6 - 26055986 26055986 26055986 GCCCAAGAAGGCGGCTGGCGGCGCAACTCCGAAGAAGAGCGCTAAGAAAACACCGAAGAAAGCGA GCCCAAGAAGGCGGCTGGCGGCGCAACTCCGAGGAAGAGCGCTAAGAAAACACCGAAGAAAGCGA T C H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26055939..26056127 26863196 MeRIP-seq:(Medium) rs1194202121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251068,Human_RBP_ID_842141,Human_RBP_ID_1668814,Human_RBP_ID_2016672,Human_RBP_ID_3804144,Human_RBP_ID_4876064,Human_RBP_ID_7585576,Human_RBP_ID_9400056,Human_RBP_ID_23059042,Human_RBP_ID_24548350,Human_RBP_ID_26353468,Human_RBP_ID_26829087,Human_RBP_ID_27093640,Human_RBP_ID_27160883,Human_RBP_ID_27343944,Human_RBP_ID_27521850 RMVar_hsa_circ_237733,RMVar_hsa_circ_237735,RMVar_hsa_circ_377187 68633 RMVar_ID_68633 Human_SNP_ID_270656282 m1A Human chr6 - 26055987 26055987 26055987 AGCCCAAGAAGGCGGCTGGCGGCGCAACTCCGAAGAAGAGCGCTAAGAAAACACCGAAGAAAGCG AGCCCAAGAAGGCGGCTGGCGGCGCAACTCCGGAGAAGAGCGCTAAGAAAACACCGAAGAAAGCG T C H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26055882..26056159 26863196 MeRIP-seq:(Medium) rs777466176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251068,Human_RBP_ID_658976,Human_RBP_ID_842141,Human_RBP_ID_1668814,Human_RBP_ID_2016672,Human_RBP_ID_3804144,Human_RBP_ID_4876064,Human_RBP_ID_7585576,Human_RBP_ID_9400056,Human_RBP_ID_23059042,Human_RBP_ID_24548350,Human_RBP_ID_26353468,Human_RBP_ID_26829088,Human_RBP_ID_27093640,Human_RBP_ID_27160883,Human_RBP_ID_27343944,Human_RBP_ID_27521850 RMVar_hsa_circ_237733,RMVar_hsa_circ_237735,RMVar_hsa_circ_377187 68634 RMVar_ID_68634 Human_SNP_ID_270656397 m1A Human chr6 - 26056079 26056079 26056079 ACTCAACAAGAAGGCAGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAAAGGCGGGCGGAACCAAAC ACTCAACAAGAAGGCAGCCTCCGGGGAAGCCACGCCCAAGGTTAAAAAGGCGGGCGGAACCAAAC T G H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26055976..26056200 32194978 MeRIP-seq:(Medium) rs1189778582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658977,Human_RBP_ID_948548,Human_RBP_ID_1045984,Human_RBP_ID_1326431,Human_RBP_ID_1668818,Human_RBP_ID_2016674,Human_RBP_ID_3804145,Human_RBP_ID_4876069,Human_RBP_ID_8639977,Human_RBP_ID_9192811,Human_RBP_ID_9400058,Human_RBP_ID_9444294,Human_RBP_ID_18860536,Human_RBP_ID_22102274,Human_RBP_ID_22309190,Human_RBP_ID_22460429,Human_RBP_ID_22772629,Human_RBP_ID_22830329,Human_RBP_ID_24387602,Human_RBP_ID_26353471,Human_RBP_ID_26714191,Human_RBP_ID_27093640,Human_RBP_ID_27343946,Human_RBP_ID_27521852 RMVar_hsa_circ_266433 68635 RMVar_ID_68635 Human_SNP_ID_270656680 m1A Human chr6 + 26056310 26056310 26056310 AGGCGGCCACAGCCTTGGTGATGAGCTCTGACACCGGGGGACCAGACGCCTTACGAGGCGTACCC AGGCGGCCACAGCCTTGGTGATGAGCTCTGACGCCGGGGGACCAGACGCCTTACGAGGCGTACCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:26056266..26056450 26863196 MeRIP-seq:(Medium) rs754218788 Functional Loss SNV dbSNP153 33..33 33 - - - 68636 RMVar_ID_68636 Human_SNP_ID_270656729 m1A Human chr6 - 26056338 26056338 26056338 TAAAGAAGAAGGCGGCCAAAAAGGCTGGGGGTACGCCTCGTAAGGCGTCTGGTCCCCCGGTGTCA TAAAGAAGAAGGCGGCCAAAAAGGCTGGGGGTGCGCCTCGTAAGGCGTCTGGTCCCCCGGTGTCA T C H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26056287..26056475 26863196 MeRIP-seq:(Medium) rs1444425351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658986,Human_RBP_ID_1045990,Human_RBP_ID_1668818,Human_RBP_ID_3804152,Human_RBP_ID_4876080,Human_RBP_ID_5511040,Human_RBP_ID_7585593,Human_RBP_ID_8269812,Human_RBP_ID_8639979,Human_RBP_ID_8899087,Human_RBP_ID_9335985,Human_RBP_ID_9400067,Human_RBP_ID_15770019,Human_RBP_ID_18071324,Human_RBP_ID_18211348,Human_RBP_ID_18449931,Human_RBP_ID_22309192,Human_RBP_ID_22460435,Human_RBP_ID_22830337,Human_RBP_ID_24153223,Human_RBP_ID_26353478,Human_RBP_ID_26534361,Human_RBP_ID_26714192,Human_RBP_ID_27093642,Human_RBP_ID_27343948,Human_RBP_ID_27521861,Human_RBP_ID_27753980 68637 RMVar_ID_68637 Human_SNP_ID_270656850 m1A Human chr6 + 26056411 26056411 26056411 TTCTCCGCAGGAGGCGCGGCAGCGGGAGCGGCAGGAGCAGTCTCGGACATGTTGAGAATCAAAAA TTCTCCGCAGGAGGCGCGGCAGCGGGAGCGGCGGGAGCAGTCTCGGACATGTTGAGAATCAAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:26056292..26056475;chr6:26056301..26056475 26863196 MeRIP-seq:(Medium) rs996475159 Functional Loss SNV dbSNP153 33..33 33 - - - 68638 RMVar_ID_68638 Human_SNP_ID_270656857 m1A Human chr6 + 26056417 26056417 26056417 GCAGGAGGCGCGGCAGCGGGAGCGGCAGGAGCAGTCTCGGACATGTTGAGAATCAAAAACTCGGG GCAGGAGGCGCGGCAGCGGGAGCGGCAGGAGCGGTCTCGGACATGTTGAGAATCAAAAACTCGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:26056298..26056475 26863196 MeRIP-seq:(Medium) rs760953453 Functional Loss SNV dbSNP153 33..33 33 - - - 68639 RMVar_ID_68639 Human_SNP_ID_270656870 m1A Human chr6 + 26056425 26056425 26056425 CGCGGCAGCGGGAGCGGCAGGAGCAGTCTCGGACATGTTGAGAATCAAAAACTCGGGTACAAGTG CGCGGCAGCGGGAGCGGCAGGAGCAGTCTCGGGCATGTTGAGAATCAAAAACTCGGGTACAAGTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26056376..26056475 26863196 MeRIP-seq:(Medium) rs1244403998 Functional Loss SNV dbSNP153 33..33 33 - - - 68640 RMVar_ID_68640 Human_SNP_ID_270665257 m1A Human chr6 - 26090953 26090953 26090953 CATGGAGTTCGGGGCTCCACACGGCGACTCTCATGATCATAGAACACGAACAGCTGGTCATCCAC CATGGAGTTCGGGGCTCCACACGGCGACTCTCGTGATCATAGAACACGAACAGCTGGTCATCCAC T C LOC108783645-001,LOC108783645-001:2 RNACentral:URS0000A77725,RNACentral:URS00008B39A7 antisense RNA,lincRNA exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26090903..26091053 32194978 MeRIP-seq:(Medium) rs147426902 Functional Loss SNV dbSNP153 33..33 33 - - - 68641 RMVar_ID_68641 Human_SNP_ID_270665368 m1A Human chr6 + 26091361 26091358 26091361 AGGTCATCCTGGGCTGTGAAATGCAAGAAGACAACAGTACCGAGGGCTACTGGAAGTACGGGTAT AGGTCATCCTGGGCTGTGAAATGCAAGAAG___ACAGTACCGAGGGCTACTGGAAGTACGGGTAT GACA G HFE Ensembl:ENSG00000010704 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:26091316..26091437 26863196 MeRIP-seq:(Medium) rs866696814 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_744984,Human_Splice_Rec_745002,Human_Splice_Rec_745024,Human_Splice_Rec_745034,Human_Splice_Rec_745062,Human_Splice_Rec_745070,Human_Splice_Rec_745080 68642 RMVar_ID_68642 Human_SNP_ID_270674706 m1A Human chr6 + 26123919 26123919 26123919 CTTGGCTGGCTCAGGCATCTTAAAACACCAGAAATGTGTCGAAAGTAAAGAGCGGATTTCTGCTA CTTGGCTGGCTCAGGCATCTTAAAACACCAGACATGTGTCGAAAGTAAAGAGCGGATTTCTGCTA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26123901..26123925 26863196 MeRIP-seq:(Medium) rs1354901311 Functional Loss SNV dbSNP153 33..33 33 - - - 68643 RMVar_ID_68643 Human_SNP_ID_270683473 m1A Human chr6 - 26156385 26156385 26156385 GGGCGCGGCAGGCGCAGTCTCGGACATGTTGAAGGCAAGCGTGAGCGAGAGCAATTCGAGCCGGA GGGCGCGGCAGGCGCAGTCTCGGACATGTTGAGGGCAAGCGTGAGCGAGAGCAATTCGAGCCGGA T C lnc-HIST1H4D-3 RNACentral:URS0000D5AA68 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:26156326..26156582;chr6:26156326..26156500 26863196 MeRIP-seq:(Medium) rs767093143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76721,RMVar_hsa_circ_237739 68644 RMVar_ID_68644 Human_SNP_ID_270683537 m1A Human chr6 + 26156437 26156437 26156437 GCCTGCCGCGCCCGCTGCTCCGGCCCCTGCCGAGAAGACTCCCGTGAAGAAGAAGGCCCGCAAGT GCCTGCCGCGCCCGCTGCTCCGGCCCCTGCCGTGAAGACTCCCGTGAAGAAGAAGGCCCGCAAGT A T H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:26156326..26156560 26863196 MeRIP-seq:(Medium) rs1434683531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252358,Human_RBP_ID_1046020,Human_RBP_ID_1326453,Human_RBP_ID_1668872,Human_RBP_ID_2016703,Human_RBP_ID_3804201,Human_RBP_ID_4876134,Human_RBP_ID_7585688,Human_RBP_ID_8640037,Human_RBP_ID_8899120,Human_RBP_ID_9335992,Human_RBP_ID_9400072,Human_RBP_ID_15770186,Human_RBP_ID_18860597,Human_RBP_ID_22513763,Human_RBP_ID_22830371,Human_RBP_ID_24548546,Human_RBP_ID_26714211,Human_RBP_ID_27093666,Human_RBP_ID_27343977 68645 RMVar_ID_68645 Human_SNP_ID_270683558 m1A Human chr6 + 26156451 26156449 26156452 CTGCTCCGGCCCCTGCCGAGAAGACTCCCGTGAAGAAGAAGGCCCGCAAGTCTGCAGGTGCGGCC CTGCTCCGGCCCCTGCCGAGAAGACTCCCGT___GAAGAAGGCCCGCAAGTCTGCAGGTGCGGCC TGAA T H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:26156351..26156492 26863410 MeRIP-seq:(Medium) rs545095988 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_659039,Human_RBP_ID_1046020,Human_RBP_ID_1668872,Human_RBP_ID_2016703,Human_RBP_ID_3804201,Human_RBP_ID_4876134,Human_RBP_ID_7585688,Human_RBP_ID_8640037,Human_RBP_ID_9335992,Human_RBP_ID_9400073,Human_RBP_ID_18860597,Human_RBP_ID_22462435,Human_RBP_ID_22830371,Human_RBP_ID_24548546,Human_RBP_ID_26353118,Human_RBP_ID_26714211,Human_RBP_ID_27093666,Human_RBP_ID_27343977 68646 RMVar_ID_68646 Human_SNP_ID_270683842 m1A Human chr6 - 26156727 26156727 26156727 TGCCTTTTTAGCCTTAGGCTTGGCTTCCCCAGAGGCCGCCTTCTTGTTGAGTTTGAAGGAACCCG TGCCTTTTTAGCCTTAGGCTTGGCTTCCCCAGCGGCCGCCTTCTTGTTGAGTTTGAAGGAACCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26156677..26156868 26863196 MeRIP-seq:(Medium) rs776535891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76721,RMVar_hsa_circ_237739 68647 RMVar_ID_68647 Human_SNP_ID_270683906 m1A Human chr6 + 26156770 26156770 26156770 CAAGCCTAAGGCTAAAAAGGCAGGCGCGGCCAAGGCCAAGAAGCCAGCAGGAGCGGCGAAGAAGC CAAGCCTAAGGCTAAAAAGGCAGGCGCGGCCAGGGCCAAGAAGCCAGCAGGAGCGGCGAAGAAGC A G H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:26156722..26156872 26863196 MeRIP-seq:(Medium) rs755687564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046028,Human_RBP_ID_4909907,Human_RBP_ID_9336495,Human_RBP_ID_24548761,Human_RBP_ID_26353480 68648 RMVar_ID_68648 Human_SNP_ID_270683946 m1A Human chr6 + 26156806 26156804 26156807 CAAGAAGCCAGCAGGAGCGGCGAAGAAGCCCAAGAAGGCGACGGGGGCGGCCACCCCCAAGAAGA CAAGAAGCCAGCAGGAGCGGCGAAGAAGCCC___AAGGCGACGGGGGCGGCCACCCCCAAGAAGA CAAG C H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:26156755..26156944 26863196 MeRIP-seq:(Medium) rs767529929 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_791099,Human_RBP_ID_4876141,Human_RBP_ID_9335994,Human_RBP_ID_9400079,Human_RBP_ID_22309241,Human_RBP_ID_24548354,Human_RBP_ID_26353121,Human_RBP_ID_27093668,Human_RBP_ID_27343981,Human_RBP_ID_27827373 68649 RMVar_ID_68649 Human_SNP_ID_270683949 m1A Human chr6 + 26156806 26156806 26156806 CAAGAAGCCAGCAGGAGCGGCGAAGAAGCCCAAGAAGGCGACGGGGGCGGCCACCCCCAAGAAGA CAAGAAGCCAGCAGGAGCGGCGAAGAAGCCCACGAAGGCGACGGGGGCGGCCACCCCCAAGAAGA A C H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:26156755..26156944 26863196 MeRIP-seq:(Medium) rs772035454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791099,Human_RBP_ID_4876141,Human_RBP_ID_9335994,Human_RBP_ID_9400079,Human_RBP_ID_22309241,Human_RBP_ID_24548354,Human_RBP_ID_26353121,Human_RBP_ID_27093668,Human_RBP_ID_27343981,Human_RBP_ID_27827373 68650 RMVar_ID_68650 Human_SNP_ID_270683951 m1A Human chr6 + 26156808 26156808 26156808 AGAAGCCAGCAGGAGCGGCGAAGAAGCCCAAGAAGGCGACGGGGGCGGCCACCCCCAAGAAGAGC AGAAGCCAGCAGGAGCGGCGAAGAAGCCCAAGGAGGCGACGGGGGCGGCCACCCCCAAGAAGAGC A G H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:26156708..26156858 26863196 MeRIP-seq:(Medium) rs1365353986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252361,Human_RBP_ID_791099,Human_RBP_ID_4876141,Human_RBP_ID_9335994,Human_RBP_ID_9400079,Human_RBP_ID_22309241,Human_RBP_ID_24548354,Human_RBP_ID_26353121,Human_RBP_ID_27093668,Human_RBP_ID_27343981,Human_RBP_ID_27827373 68651 RMVar_ID_68651 Human_SNP_ID_270683979 m1A Human chr6 + 26156847 26156825 26156848 CGGGGGCGGCCACCCCCAAGAAGAGCGCCAAGAAGACCCCAAAGAAGGCGAAGAAGCCGGCTGCA CGGGGGCGGCC_______________________GACCCCAAAGAAGGCGAAGAAGCCGGCTGCA CACCCCCAAGAAGAGCGCCAAGAA C H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26156671..26157031 26863196 MeRIP-seq:(Medium) rs1131690807 Functional Loss DEL dbSNP153 12..34 33 - - - Human_RBP_ID_214841,Human_RBP_ID_1668878,Human_RBP_ID_2016709,Human_RBP_ID_4909907,Human_RBP_ID_8640045,Human_RBP_ID_18860611,Human_RBP_ID_24548354,Human_RBP_ID_26354796,Human_RBP_ID_27093668,Human_RBP_ID_27343982,Human_RBP_ID_27828324 Clinvar_Rec_277,Clinvar_Rec_2413 68652 RMVar_ID_68652 Human_SNP_ID_270683999 m1A Human chr6 + 26156838 26156838 26156838 AGAAGGCGACGGGGGCGGCCACCCCCAAGAAGAGCGCCAAGAAGACCCCAAAGAAGGCGAAGAAG AGAAGGCGACGGGGGCGGCCACCCCCAAGAAGGGCGCCAAGAAGACCCCAAAGAAGGCGAAGAAG A G H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26156669..26157034 26863196 MeRIP-seq:(Medium) rs1237671443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252361,Human_RBP_ID_1668878,Human_RBP_ID_4909907,Human_RBP_ID_8640045,Human_RBP_ID_18860611,Human_RBP_ID_24548354,Human_RBP_ID_26353481,Human_RBP_ID_27093668,Human_RBP_ID_27343982,Human_RBP_ID_27827373 68653 RMVar_ID_68653 Human_SNP_ID_270685056 m1A Human chr6 - 26158188 26158188 26158188 CTTCTTGGAGCCCTTCTTTGGGGCAGGAGCAGACTTGGTAGGTTCAGGCATCGTAGCGTTAATAG CTTCTTGGAGCCCTTCTTTGGGGCAGGAGCAGTCTTGGTAGGTTCAGGCATCGTAGCGTTAATAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:26158126..26158350;chr6:26158126..26158287;chr6:26158126..26158400;chr6:26158126..26158300;chr6:26158126..26158325 26863196 MeRIP-seq:(Medium) rs1202875011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_93634,RMVar_hsa_circ_237741 68654 RMVar_ID_68654 Human_SNP_ID_270685103 m1A Human chr6 + 26158243 26158243 26158243 CTCCAAGAAGGCGGTGACTAAGGCTCAGAAGAAGGACGGGAAGAAGCGCAAGCGCAGCCGCAAGG CTCCAAGAAGGCGGTGACTAAGGCTCAGAAGAGGGACGGGAAGAAGCGCAAGCGCAGCCGCAAGG A G H2BC5 Ensembl:ENSG00000158373 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26158193..26158388 32194978 MeRIP-seq:(Medium) rs774818397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81820,Human_RBP_ID_252340,Human_RBP_ID_1668890,Human_RBP_ID_2016714,Human_RBP_ID_3000952,Human_RBP_ID_3804210,Human_RBP_ID_4876151,Human_RBP_ID_5428204,Human_RBP_ID_5617696,Human_RBP_ID_7585717,Human_RBP_ID_8640055,Human_RBP_ID_8899142,Human_RBP_ID_9335995,Human_RBP_ID_9400082,Human_RBP_ID_15770232,Human_RBP_ID_17710134,Human_RBP_ID_18538975,Human_RBP_ID_18860626,Human_RBP_ID_22460455,Human_RBP_ID_22830385,Human_RBP_ID_26353125,Human_RBP_ID_26534445,Human_RBP_ID_26714218,Human_RBP_ID_27093680,Human_RBP_ID_27343987,Human_RBP_ID_27521922 68655 RMVar_ID_68655 Human_SNP_ID_270685123 m1A Human chr6 + 26158272 26158272 26158272 AGAAGGACGGGAAGAAGCGCAAGCGCAGCCGCAAGGAGAGCTATTCAGTGTATGTGTACAAGGTG AGAAGGACGGGAAGAAGCGCAAGCGCAGCCGCCAGGAGAGCTATTCAGTGTATGTGTACAAGGTG A C H2BC5 Ensembl:ENSG00000158373 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:26158173..26158323 26863196 MeRIP-seq:(Medium) rs142728540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252340,Human_RBP_ID_659054,Human_RBP_ID_1113045,Human_RBP_ID_1668890,Human_RBP_ID_2016714,Human_RBP_ID_5428204,Human_RBP_ID_7585720,Human_RBP_ID_8640057,Human_RBP_ID_9400083,Human_RBP_ID_15770240,Human_RBP_ID_22309256,Human_RBP_ID_22462440,Human_RBP_ID_26353126,Human_RBP_ID_26540896,Human_RBP_ID_27093680,Human_RBP_ID_27343987 68656 RMVar_ID_68656 Human_SNP_ID_270696357 m1A Human chr6 + 26197227 26197227 26197227 TTGCGTGGCGCTTTCCCACCCGTGGACTTGCGAGCAGTCTGCTTGGTACGAGCCATTGCGAACTT TTGCGTGGCGCTTTCCCACCCGTGGACTTGCGCGCAGTCTGCTTGGTACGAGCCATTGCGAACTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26197072..26197275 26863196 MeRIP-seq:(Medium) rs1257048763 Functional Loss SNV dbSNP153 33..33 33 - - - 68657 RMVar_ID_68657 Human_SNP_ID_270697460 m1A Human chr6 - 26199263 26199263 26199263 TCACTTTTACATTTTTGTCTTCATTGCTTAACATCGTTTTTAAGAATTCAAAATGTCCGGACGCG TCACTTTTACATTTTTGTCTTCATTGCTTAACGTCGTTTTTAAGAATTCAAAATGTCCGGACGCG T C AL031777.2,H2AC7 Ensembl:ENSG00000282988,Ensembl:ENSG00000196866 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26199251..26199275 26863196 MeRIP-seq:(Medium) rs201050533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_314057,Human_RBP_ID_1216619,Human_RBP_ID_1394705,Human_RBP_ID_1668949,Human_RBP_ID_2016747,Human_RBP_ID_3000997,Human_RBP_ID_3804259,Human_RBP_ID_4903733,Human_RBP_ID_5276627,Human_RBP_ID_5450895,Human_RBP_ID_5477790,Human_RBP_ID_9336502,Human_RBP_ID_15770399,Human_RBP_ID_18170913,Human_RBP_ID_22106326,Human_RBP_ID_22309290,Human_RBP_ID_24435439,Human_RBP_ID_24511901,Human_RBP_ID_26534483,Human_RBP_ID_27093699,Human_RBP_ID_27344020 RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_93634,RMVar_hsa_circ_237741 68658 RMVar_ID_68658 Human_SNP_ID_270697748 m1A Human chr6 + 26199640 26199640 26199640 AGGCGGTGACCAAGGCGCAGAAGAAGGATGGTAAGAAGCGCAAGCGTAGCCGCAAGGAGAGCTAT AGGCGGTGACCAAGGCGCAGAAGAAGGATGGTGAGAAGCGCAAGCGTAGCCGCAAGGAGAGCTAT A G H2BC7 Ensembl:ENSG00000277224 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26199526..26199740 26863196 MeRIP-seq:(Medium) rs1263306640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792285,Human_RBP_ID_4876255,Human_RBP_ID_18195676,Human_RBP_ID_22460467,Human_RBP_ID_22706230,Human_RBP_ID_26353488,Human_RBP_ID_27344024 68659 RMVar_ID_68659 Human_SNP_ID_270697749 m1A Human chr6 + 26199640 26199640 26199640 AGGCGGTGACCAAGGCGCAGAAGAAGGATGGTAAGAAGCGCAAGCGTAGCCGCAAGGAGAGCTAT AGGCGGTGACCAAGGCGCAGAAGAAGGATGGTTAGAAGCGCAAGCGTAGCCGCAAGGAGAGCTAT A T H2BC7 Ensembl:ENSG00000277224 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26199526..26199740 26863196 MeRIP-seq:(Medium) rs1263306640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792285,Human_RBP_ID_4876255,Human_RBP_ID_18195676,Human_RBP_ID_22460467,Human_RBP_ID_22706230,Human_RBP_ID_26353488,Human_RBP_ID_27344024 68660 RMVar_ID_68660 Human_SNP_ID_270699612 m1A Human chr6 - 26204820 26204820 26204820 CATCACGAATCACGTTTTCCAGAAACACCTTCAGAACCCCGCGAGTCTCCTCGTAGATGAGACCA CATCACGAATCACGTTTTCCAGAAACACCTTCGGAACCCCGCGAGTCTCCTCGTAGATGAGACCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26204770..26204849 32194978 MeRIP-seq:(Medium) rs374281617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76721,RMVar_hsa_circ_237739 68661 RMVar_ID_68661 Human_SNP_ID_270703497 m1A Human chr6 - 26216570 26216568 26216571 TTCCAAGAAGGCTGTGACCAAGGCGCAGAAGAAGGATGGCAAGAAGCGCAAGCGCAGTCGTAAGG TTCCAAGAAGGCTGTGACCAAGGCGCAGAAG___GATGGCAAGAAGCGCAAGCGCAGTCGTAAGG CCTT C H2BC8 Ensembl:ENSG00000273802 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26216519..26216643 26863196 MeRIP-seq:(Medium) rs763480943 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1111442,Human_RBP_ID_4905376,Human_RBP_ID_5478663,Human_RBP_ID_9336001,Human_RBP_ID_9400099,Human_RBP_ID_22104720,Human_RBP_ID_22460481,Human_RBP_ID_24548356,Human_RBP_ID_26353130 RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_237747,RMVar_hsa_circ_378737 68662 RMVar_ID_68662 Human_SNP_ID_270703811 m1A Human chr6 + 26216995 26216995 26216995 TAGGAAGCCACTATGTCTGGACGTGGAAAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCG TAGGAAGCCACTATGTCTGGACGTGGAAAGCAGGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCG A G H2AC8 Ensembl:ENSG00000277075 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26216976..26217000 26863196 MeRIP-seq:(Medium) rs1181844610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791812,Human_RBP_ID_22462474,Human_RBP_ID_23214688,Human_RBP_ID_24437165 68663 RMVar_ID_68663 Human_SNP_ID_270703838 m1A Human chr6 + 26217022 26217022 26217022 AAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCGTTCTTCCAGGGCCGGTCTTCAGTTTCC AAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAGACGCGTTCTTCCAGGGCCGGTCTTCAGTTTCC A G H2AC8 Ensembl:ENSG00000277075 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:26217001..26217025 26863196 MeRIP-seq:(Medium) rs1217103958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4876312 68664 RMVar_ID_68664 Human_SNP_ID_270714915 m1A Human chr6 + 26251700 26251700 26251700 GTCCGCTCCCGCCCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCGCAGAAGAAGGATGGCA GTCCGCTCCCGCCCCGAAGAAGGGCTCCAAGAGGGCGGTGACCAAGGCGCAGAAGAAGGATGGCA A G H2BC9 Ensembl:ENSG00000275713 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26251676..26251700 26863196 MeRIP-seq:(Medium) rs1343727126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5478665,Human_RBP_ID_22461696,Human_RBP_ID_22706110,Human_RBP_ID_26353496,Human_RBP_ID_26828013 68665 RMVar_ID_68665 Human_SNP_ID_270714924 m1A Human chr6 + 26251712 26251712 26251712 CCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCGCAGAAGAAGGATGGCAAGAAGCGTAAAC CCCGAAGAAGGGCTCCAAGAAGGCGGTGACCACGGCGCAGAAGAAGGATGGCAAGAAGCGTAAAC A C H2BC9 Ensembl:ENSG00000275713 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26251661..26251787 26863196 MeRIP-seq:(Medium) rs1561759702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5478665,Human_RBP_ID_22461696,Human_RBP_ID_22706110,Human_RBP_ID_26353496,Human_RBP_ID_26828013 68666 RMVar_ID_68666 Human_SNP_ID_270715545 m1A Human chr6 + 26253373 26253373 26253373 TTCTGGAGGGAGGGTGGAGCAAAAGAGATGGCAGAAGAAGAGGAGCCAGCAGCACTGGAATTCAA TTCTGGAGGGAGGGTGGAGCAAAAGAGATGGCGGAAGAAGAGGAGCCAGCAGCACTGGAATTCAA A G H2BC9 Ensembl:ENSG00000275713 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26253342..26253478 26863196 MeRIP-seq:(Medium) rs1338772476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5152054 68667 RMVar_ID_68667 Human_SNP_ID_270720797 m1A Human chr6 - 26272990 26272990 26272990 TTGGAGCCCTTCTTCGGGGCGGGAGCTGACTTAGCTGGTTCAGGCATGTTCGCAGCCGAAGTGAT TTGGAGCCCTTCTTCGGGGCGGGAGCTGACTTGGCTGGTTCAGGCATGTTCGCAGCCGAAGTGAT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr6:26272926..26273075;chr6:26272951..26273050 26863196 MeRIP-seq:(Medium) rs1411693434 Functional Loss SNV dbSNP153 33..33 33 - - - 68668 RMVar_ID_68668 Human_SNP_ID_270720798 m1A Human chr6 - 26272990 26272990 26272990 TTGGAGCCCTTCTTCGGGGCGGGAGCTGACTTAGCTGGTTCAGGCATGTTCGCAGCCGAAGTGAT TTGGAGCCCTTCTTCGGGGCGGGAGCTGACTTCGCTGGTTCAGGCATGTTCGCAGCCGAAGTGAT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr6:26272926..26273075;chr6:26272951..26273050 26863196 MeRIP-seq:(Medium) rs1411693434 Functional Loss SNV dbSNP153 33..33 33 - - - 68669 RMVar_ID_68669 Human_SNP_ID_270720818 m1A Human chr6 + 26273012 26273012 26273012 CTGAACCAGCTAAGTCAGCTCCCGCCCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCACAG CTGAACCAGCTAAGTCAGCTCCCGCCCCGAAGCAGGGCTCCAAGAAGGCGGTGACCAAGGCACAG A C H2BC10 Ensembl:ENSG00000278588 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26272963..26273071 26863196 MeRIP-seq:(Medium) rs1189108232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9400106 68670 RMVar_ID_68670 Human_SNP_ID_270720829 m1A Human chr6 + 26273025 26273025 26273025 GTCAGCTCCCGCCCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCACAGAAGAAGGATGGCA GTCAGCTCCCGCCCCGAAGAAGGGCTCCAAGACGGCGGTGACCAAGGCACAGAAGAAGGATGGCA A C H2BC10 Ensembl:ENSG00000278588 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26272978..26273122 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9400106 68671 RMVar_ID_68671 Human_SNP_ID_270724008 m1A Human chr6 - 26285345 26285345 26285345 CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTATGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTTTGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC T A H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26285294..26285550 26863196 MeRIP-seq:(Medium) rs751532587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81823,Human_RBP_ID_659146,Human_RBP_ID_1046113,Human_RBP_ID_1216636,Human_RBP_ID_1326475,Human_RBP_ID_1668995,Human_RBP_ID_2016774,Human_RBP_ID_3804296,Human_RBP_ID_4876438,Human_RBP_ID_5219128,Human_RBP_ID_5428224,Human_RBP_ID_7586022,Human_RBP_ID_8640146,Human_RBP_ID_8899189,Human_RBP_ID_9336005,Human_RBP_ID_15770525,Human_RBP_ID_17306023,Human_RBP_ID_17419225,Human_RBP_ID_17535179,Human_RBP_ID_18071499,Human_RBP_ID_18369501,Human_RBP_ID_18449944,Human_RBP_ID_18860708,Human_RBP_ID_22773296,Human_RBP_ID_23137943,Human_RBP_ID_24153438,Human_RBP_ID_26828017,Human_RBP_ID_27093755,Human_RBP_ID_27344070,Human_RBP_ID_27754056 68672 RMVar_ID_68672 Human_SNP_ID_270724009 m1A Human chr6 - 26285345 26285345 26285345 CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTATGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTGTGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC T C H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26285294..26285550 26863196 MeRIP-seq:(Medium) rs751532587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81823,Human_RBP_ID_659146,Human_RBP_ID_1046113,Human_RBP_ID_1216636,Human_RBP_ID_1326475,Human_RBP_ID_1668995,Human_RBP_ID_2016774,Human_RBP_ID_3804296,Human_RBP_ID_4876438,Human_RBP_ID_5219128,Human_RBP_ID_5428224,Human_RBP_ID_7586022,Human_RBP_ID_8640146,Human_RBP_ID_8899189,Human_RBP_ID_9336005,Human_RBP_ID_15770525,Human_RBP_ID_17306023,Human_RBP_ID_17419225,Human_RBP_ID_17535179,Human_RBP_ID_18071499,Human_RBP_ID_18369501,Human_RBP_ID_18449944,Human_RBP_ID_18860708,Human_RBP_ID_22773296,Human_RBP_ID_23137943,Human_RBP_ID_24153438,Human_RBP_ID_26828017,Human_RBP_ID_27093755,Human_RBP_ID_27344070,Human_RBP_ID_27754056 68673 RMVar_ID_68673 Human_SNP_ID_270724023 m1A Human chr6 - 26285362 26285362 26285362 CGGCGCCTTGCTCGTCGCGGCGGTGTCAAGCGAATTTCTGGCCTTATCTATGAGGAGACTCGTGG CGGCGCCTTGCTCGTCGCGGCGGTGTCAAGCGTATTTCTGGCCTTATCTATGAGGAGACTCGTGG T A H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:26285312..26285540;chr6:26285313..26285525 26863196 MeRIP-seq:(Medium) rs753793760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046113,Human_RBP_ID_1326476,Human_RBP_ID_1668995,Human_RBP_ID_2016774,Human_RBP_ID_3804296,Human_RBP_ID_4876438,Human_RBP_ID_7586022,Human_RBP_ID_8640146,Human_RBP_ID_8899189,Human_RBP_ID_9336005,Human_RBP_ID_15770525,Human_RBP_ID_17306023,Human_RBP_ID_17535179,Human_RBP_ID_18071500,Human_RBP_ID_18860708,Human_RBP_ID_22309336,Human_RBP_ID_22460489,Human_RBP_ID_22773296,Human_RBP_ID_23137943,Human_RBP_ID_24153440,Human_RBP_ID_26534540,Human_RBP_ID_26828018,Human_RBP_ID_27344070,Human_RBP_ID_27754056 68674 RMVar_ID_68674 Human_SNP_ID_270724074 m1A Human chr6 - 26285426 26285426 26285426 AGGAGCTAAGCGTCATCGCAAGGTTTTGCGCGATAACATCCAGGGCATCACTAAGCCAGCTATCC AGGAGCTAAGCGTCATCGCAAGGTTTTGCGCGGTAACATCCAGGGCATCACTAAGCCAGCTATCC T C H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26285376..26285525 26863196 MeRIP-seq:(Medium) rs748128721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358,Human_RBP_ID_1216637,Human_RBP_ID_1668995,Human_RBP_ID_2016778,Human_RBP_ID_4876438,Human_RBP_ID_5121852,Human_RBP_ID_5327073,Human_RBP_ID_5511100,Human_RBP_ID_7586028,Human_RBP_ID_8141033,Human_RBP_ID_8640148,Human_RBP_ID_8899191,Human_RBP_ID_9192883,Human_RBP_ID_9336514,Human_RBP_ID_17306024,Human_RBP_ID_17535180,Human_RBP_ID_18071500,Human_RBP_ID_18860713,Human_RBP_ID_22460489,Human_RBP_ID_22482261,Human_RBP_ID_22706119,Human_RBP_ID_22773296,Human_RBP_ID_22830432,Human_RBP_ID_23214691,Human_RBP_ID_24548548,Human_RBP_ID_27344070,Human_RBP_ID_27754058,Human_RBP_ID_27842381 68675 RMVar_ID_68675 Human_SNP_ID_270724141 m1A Human chr6 + 26285494 26285494 26285494 TTACCCAAACCTTTTCCACCTTTACCACGGCCAGACATGACTAAGCAACTTCTAAAACCAACTTA TTACCCAAACCTTTTCCACCTTTACCACGGCCCGACATGACTAAGCAACTTCTAAAACCAACTTA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26285451..26285525 26863196 MeRIP-seq:(Medium) rs1287974209 Functional Loss SNV dbSNP153 33..33 33 - - - 68676 RMVar_ID_68676 Human_SNP_ID_270724142 m1A Human chr6 + 26285494 26285494 26285494 TTACCCAAACCTTTTCCACCTTTACCACGGCCAGACATGACTAAGCAACTTCTAAAACCAACTTA TTACCCAAACCTTTTCCACCTTTACCACGGCCGGACATGACTAAGCAACTTCTAAAACCAACTTA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26285451..26285525 26863196 MeRIP-seq:(Medium) rs1287974209 Functional Loss SNV dbSNP153 33..33 33 - - - 68677 RMVar_ID_68677 Human_SNP_ID_270724143 m1A Human chr6 + 26285494 26285494 26285494 TTACCCAAACCTTTTCCACCTTTACCACGGCCAGACATGACTAAGCAACTTCTAAAACCAACTTA TTACCCAAACCTTTTCCACCTTTACCACGGCCTGACATGACTAAGCAACTTCTAAAACCAACTTA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26285451..26285525 26863196 MeRIP-seq:(Medium) rs1287974209 Functional Loss SNV dbSNP153 33..33 33 - - - 68678 RMVar_ID_68678 Human_SNP_ID_270724706 m1A Human chr6 + 26286582 26286582 26286582 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTAGGTCCTTTTTTTTTCTC GCTGGGCCCATAACCCAGAGGTCGATGGATCGCAACCATCCTCTGCTAGGTCCTTTTTTTTTCTC A C tRNA-iMet-CAT-1-1,TRX-CAT1-1,lnc-HIST1H2BI-2,lnc-HIST1H2BI-2:2,lnc-HIST1H2BI-2:3,lnc-HIST1H2BI-2:4 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC,RNACentral:URS0000D58C15,RNACentral:URS0000D5995E,RNACentral:URS0000D5C608,RNACentral:URS0000D5A318 tRNA,tRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs953412324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326477,Human_RBP_ID_1394715,Human_RBP_ID_1669007,Human_RBP_ID_5276631,Human_RBP_ID_8640151,Human_RBP_ID_18174236,Human_RBP_ID_18860717,Human_RBP_ID_22102367,Human_RBP_ID_22830434,Human_RBP_ID_23137949,Human_RBP_ID_27093758 68679 RMVar_ID_68679 Human_SNP_ID_270727699 m1A Human chr6 + 26299734 26299734 26299734 GTCTGACTTCGGATCAGAAGATTGAGGGTTCGAATCCCTTCGTGGTTAAGTGGGGTTCGTTTTCG GTCTGACTTCGGATCAGAAGATTGAGGGTTCGCATCCCTTCGTGGTTAAGTGGGGTTCGTTTTCG A C tRNA-Arg-TCG-4-1,tRNA-Arg,lnc-HIST1H2BI-2 RNACentral:URS0000677EA0,RNACentral:URS000003B38D,RNACentral:URS0000D5C608 tRNA,tRNA,lincRNA exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs993864047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669011,Human_RBP_ID_8640156,Human_RBP_ID_10278129,Human_RBP_ID_18860722,Human_RBP_ID_21315180,Human_RBP_ID_22830436,Human_RBP_ID_23059093,Human_RBP_ID_23137952,Human_RBP_ID_25992633 68680 RMVar_ID_68680 Human_SNP_ID_270729074 m1A Human chr6 - 26305505 26305505 26305505 CTAATCCATTGTGCTCTGCACGCGTGGGTTCGAATCCCATCCTCGTCGCTCGGCTTTCCCTGCTA CTAATCCATTGTGCTCTGCACGCGTGGGTTCGTATCCCATCCTCGTCGCTCGGCTTTCCCTGCTA T A tRNA-Ser-GCT-6-1,TRS-GCT6-1 RNACentral:URS0000733374,RNACentral:URS000070FB80 tRNA,tRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1275757433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659154,Human_RBP_ID_1216643,Human_RBP_ID_1669014,Human_RBP_ID_3804302,Human_RBP_ID_5216201,Human_RBP_ID_5251110,Human_RBP_ID_5428227,Human_RBP_ID_5450904,Human_RBP_ID_5477801,Human_RBP_ID_5511102,Human_RBP_ID_7586039,Human_RBP_ID_8640159,Human_RBP_ID_8899195,Human_RBP_ID_10313096,Human_RBP_ID_15770540,Human_RBP_ID_18071505,Human_RBP_ID_18202481,Human_RBP_ID_18210942,Human_RBP_ID_18449945,Human_RBP_ID_18860728,Human_RBP_ID_21315185,Human_RBP_ID_22102368,Human_RBP_ID_22309341,Human_RBP_ID_22830441,Human_RBP_ID_23059096,Human_RBP_ID_23137956,Human_RBP_ID_23194944,Human_RBP_ID_24179596,Human_RBP_ID_24437408,Human_RBP_ID_24513759,Human_RBP_ID_26045645,Human_RBP_ID_26540449,Human_RBP_ID_26751341,Human_RBP_ID_27093761,Human_RBP_ID_27160937,Human_RBP_ID_27522011 68681 RMVar_ID_68681 Human_SNP_ID_270731264 m1A Human chr6 - 26313139 26313139 26313139 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTATATGGCCGCATATATTT GCTGGGCCCATAACCCAGAGGTCGATGGATCGTAACCATCCTCTGCTATATGGCCGCATATATTT T A tRNA-iMet-CAT-1-1,TRX-CAT1-1 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1184779590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669034,Human_RBP_ID_8640174,Human_RBP_ID_18860747,Human_RBP_ID_21315208,Human_RBP_ID_23137980 68682 RMVar_ID_68682 Human_SNP_ID_270732895 m1A Human chr6 - 26319194 26319194 26319194 GGAGGAGGATAAGATTAGATACTTATCTTAAAAGGAAAATGGAGGGTCTCCGTGACCTCGTGGCG GGAGGAGGATAAGATTAGATACTTATCTTAAACGGAAAATGGAGGGTCTCCGTGACCTCGTGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26319191..26319260 26863196 MeRIP-seq:(Medium) rs1182764675 Functional Loss SNV dbSNP153 33..33 33 - - - 68683 RMVar_ID_68683 Human_SNP_ID_270733975 m1A Human chr6 - 26322948 26322948 26322948 GATAACTTAGTGAAGTAAATGGAAAGAAGTACATTTCTGATTACCAGCTTTGAGGAAGGAAAATA GATAACTTAGTGAAGTAAATGGAAAGAAGTACGTTTCTGATTACCAGCTTTGAGGAAGGAAAATA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr6:26322898..26323057;chr6:26322897..26323148 26863196 MeRIP-seq:(Medium) rs1256609192 Functional Loss SNV dbSNP153 33..33 33 - - - 68684 RMVar_ID_68684 Human_SNP_ID_270734001 m1A Human chr6 + 26323025 26323025 26323025 CCCTTCCTTCACATCCCTTGCCTTTGCTCTGTACTTAGTCTGTTTATCCTCTCTCTCTCCACCAT CCCTTCCTTCACATCCCTTGCCTTTGCTCTGTGCTTAGTCTGTTTATCCTCTCTCTCTCCACCAT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26322889..26323071 26863196 MeRIP-seq:(Medium) rs1361928576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21392864 68685 RMVar_ID_68685 Human_SNP_ID_270735138 m1A Human chr6 + 26327655 26327655 26327655 GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGAATCCTGCCGACTACGGCAGTGGGTTTTTGCAT GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGGATCCTGCCGACTACGGCAGTGGGTTTTTGCAT A G AL021917.1 Ensembl:ENSG00000287050 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1344347067 Functional Loss SNV dbSNP153 33..33 33 - - - 68686 RMVar_ID_68686 Human_SNP_ID_270736034 m1A Human chr6 - 26330316 26330316 26330316 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTAGGGAGCGTTTTGTGGAT GCTGGGCCCATAACCCAGAGGTCGATGGATCGGAACCATCCTCTGCTAGGGAGCGTTTTGTGGAT T C AL021917.1 Ensembl:ENSG00000287050 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1055932412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669052,Human_RBP_ID_5276637,Human_RBP_ID_5622211,Human_RBP_ID_10278134,Human_RBP_ID_18860770,Human_RBP_ID_21221512,Human_RBP_ID_22102377,Human_RBP_ID_22832609,Human_RBP_ID_23138013,Human_RBP_ID_27102641,Human_RBP_ID_27522020 68687 RMVar_ID_68687 Human_SNP_ID_270748770 m1A Human chr6 + 26382721 26382720 26382721 GAAAGAAAGAAAGGAAGGAGAAGAGAAGGAAGAGAAAGAGAGAAAGGAAGAGAGAGGAAGGAAGG GAAAGAAAGAAAGGAAGGAGAAGAGAAGGAAG_GAAAGAGAGAAAGGAAGAGAGAGGAAGGAAGG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26382713..26382862 26863196 MeRIP-seq:(Medium) rs1561820768 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_237752,RMVar_hsa_circ_237753 68688 RMVar_ID_68688 Human_SNP_ID_270748793 m1A Human chr6 + 26382769 26382769 26382769 AGAGAGAGGAAGGAAGGAAGGAAGAAAAAAGAAAGAAAGCGAGAAAGAAAGAAAGAATAAAGTGA AGAGAGAGGAAGGAAGGAAGGAAGAAAAAAGAGAGAAAGCGAGAAAGAAAGAAAGAATAAAGTGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26382730..26382814 26863196 MeRIP-seq:(Medium) rs28465559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237752,RMVar_hsa_circ_237753 68689 RMVar_ID_68689 Human_SNP_ID_270751364 m1A Human chr6 + 26393039 26393039 26393039 GGCCATCTCAGCAGCCACCGCACAACCCCCCTAATGAAAGACACGCCCTCCTCCCCTCTGGTCAC GGCCATCTCAGCAGCCACCGCACAACCCCCCTGATGAAAGACACGCCCTCCTCCCCTCTGGTCAC A G BTN2A2 Ensembl:ENSG00000124508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26392988..26393110 26863196 MeRIP-seq:(Medium) rs978236120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237752,RMVar_hsa_circ_237753 68690 RMVar_ID_68690 Human_SNP_ID_270751440 m1A Human chr6 + 26393395 26393395 26393395 GAGAGGAGAGAGGAATCCACAGGACCACCAGAAGGGAGAGGGAACCAGATATGCAGATCAGAGAT GAGAGGAGAGAGGAATCCACAGGACCACCAGAGGGGAGAGGGAACCAGATATGCAGATCAGAGAT A G BTN2A2 Ensembl:ENSG00000124508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26393348..26393432 26863196 MeRIP-seq:(Medium) rs955307402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237752,RMVar_hsa_circ_237753 68691 RMVar_ID_68691 Human_SNP_ID_270754445 m1A Human chr6 - 26407751 26407751 26407751 GTTGTTGCTCCACTGTATTTGGGGTTGGGGGTACCAGCCAGTGGACCTGCACTCCAGATGGATCC GTTGTTGCTCCACTGTATTTGGGGTTGGGGGTGCCAGCCAGTGGACCTGCACTCCAGATGGATCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26407701..26407750 32194978 MeRIP-seq:(Medium) rs764942378 Functional Loss SNV dbSNP153 33..33 33 - - - 68692 RMVar_ID_68692 Human_SNP_ID_270754446 m1A Human chr6 - 26407751 26407751 26407751 GTTGTTGCTCCACTGTATTTGGGGTTGGGGGTACCAGCCAGTGGACCTGCACTCCAGATGGATCC GTTGTTGCTCCACTGTATTTGGGGTTGGGGGTCCCAGCCAGTGGACCTGCACTCCAGATGGATCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26407701..26407750 32194978 MeRIP-seq:(Medium) rs764942378 Functional Loss SNV dbSNP153 33..33 33 - - - 68693 RMVar_ID_68693 Human_SNP_ID_270757718 m1A Human chr6 + 26421570 26421570 26421570 CTGGAAAGGTTGGAGACTTGGGGGACGACTGGAGAATTGCCATTTGAGGACCAAAGGAGAAAAGA CTGGAAAGGTTGGAGACTTGGGGGACGACTGGCGAATTGCCATTTGAGGACCAAAGGAGAAAAGA A C BTN2A3P Ensembl:ENSG00000124549 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26421470..26422134 26863196 MeRIP-seq:(Medium) rs537014218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5104485,Human_RBP_ID_5618363,Human_RBP_ID_9438639,Human_RBP_ID_17422242,Human_RBP_ID_18539720 Human_Splice_Rec_745571 RMVar_hsa_circ_237753,RMVar_hsa_circ_237755 68694 RMVar_ID_68694 Human_SNP_ID_270757719 m1A Human chr6 + 26421570 26421570 26421570 CTGGAAAGGTTGGAGACTTGGGGGACGACTGGAGAATTGCCATTTGAGGACCAAAGGAGAAAAGA CTGGAAAGGTTGGAGACTTGGGGGACGACTGGGGAATTGCCATTTGAGGACCAAAGGAGAAAAGA A G BTN2A3P Ensembl:ENSG00000124549 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26421470..26422134 26863196 MeRIP-seq:(Medium) rs537014218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5104485,Human_RBP_ID_5618363,Human_RBP_ID_9438639,Human_RBP_ID_17422242,Human_RBP_ID_18539720 Human_Splice_Rec_745571 RMVar_hsa_circ_237753,RMVar_hsa_circ_237755 68695 RMVar_ID_68695 Human_SNP_ID_270780771 m1A Human chr6 + 26521275 26521275 26521275 AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGAATCCCACTCCTGACAGTTCGTACTTTTAGTAT AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGCATCCCACTCCTGACAGTTCGTACTTTTAGTAT A C LOC285819 RNACentral:URS00009B2436 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs899492139 Functional Loss SNV dbSNP153 33..33 33 - - - 68696 RMVar_ID_68696 Human_SNP_ID_270780772 m1A Human chr6 + 26521275 26521275 26521275 AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGAATCCCACTCCTGACAGTTCGTACTTTTAGTAT AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGGATCCCACTCCTGACAGTTCGTACTTTTAGTAT A G LOC285819 RNACentral:URS00009B2436 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs899492139 Functional Loss SNV dbSNP153 33..33 33 - - - 68697 RMVar_ID_68697 Human_SNP_ID_270786598 m1A Human chr6 - 26545112 26545112 26545112 CTGTTCCTGGAAAGATGTCTTTAACAAGACACAAAAAGCGTAAACCATAAAGGGAAAGACTGACG CTGTTCCTGGAAAGATGTCTTTAACAAGACACCAAAAGCGTAAACCATAAAGGGAAAGACTGACG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26545110..26545223 26863196 MeRIP-seq:(Medium) rs1475160184 Functional Loss SNV dbSNP153 33..33 33 - - - 68698 RMVar_ID_68698 Human_SNP_ID_270786633 m1A Human chr6 + 26545239 26545239 26545239 ATGCCCAAGAGAAAGGCAAAAGGAGATGCTAAAGGTGATAAAGCAAAGGTGAAGGATGAGCCACA ATGCCCAAGAGAAAGGCAAAAGGAGATGCTAAGGGTGATAAAGCAAAGGTGAAGGATGAGCCACA A G HMGN4 Ensembl:ENSG00000182952 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26545121..26545279 26863196 MeRIP-seq:(Medium) rs1476034905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669102,Human_RBP_ID_3804372,Human_RBP_ID_9400112,Human_RBP_ID_18449957,Human_RBP_ID_24153667 RMVar_hsa_circ_82159,RMVar_hsa_circ_237762 68699 RMVar_ID_68699 Human_SNP_ID_270789455 m1A Human chr6 + 26555424 26555424 26555424 TATAAGTTAAAACTTGCCAGTTAGAAGCGCCGATAATTGTGGCATCGATATGCGTTAGAAACCAA TATAAGTTAAAACTTGCCAGTTAGAAGCGCCGGTAATTGTGGCATCGATATGCGTTAGAAACCAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:26555351..26555435 26863196 MeRIP-seq:(Medium) rs1325698166 Functional Loss SNV dbSNP153 33..33 33 - - - 68700 RMVar_ID_68700 Human_SNP_ID_270789914 m1A Human chr6 + 26556603 26556603 26556603 ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGAGCCCCACGTTGGGCGCTCTGGTTTTCAATCCT ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGGGCCCCACGTTGGGCGCTCTGGTTTTCAATCCT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1245335663 Functional Loss SNV dbSNP153 33..33 33 - - - 68701 RMVar_ID_68701 Human_SNP_ID_270793732 m1A Human chr6 - 26571728 26571728 26571728 ATAATGGGGGTGGTCTTTCCTTCAAGCTCAAGATTCTCTCACCACCCATGAAAACCCATCTACTC ATAATGGGGGTGGTCTTTCCTTCAAGCTCAAGGTTCTCTCACCACCCATGAAAACCCATCTACTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:26571722..26571853 26863196 MeRIP-seq:(Medium) rs1279734968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18071615 68702 RMVar_ID_68702 Human_SNP_ID_270793736 m1A Human chr6 + 26571744 26571744 26571744 ATGGGTGGTGAGAGAATCTTGAGCTTGAAGGAAAGACCACCCCCATTATGATACGGGAGTGTGTT ATGGGTGGTGAGAGAATCTTGAGCTTGAAGGAGAGACCACCCCCATTATGATACGGGAGTGTGTT A G AL121936.1 Ensembl:ENSG00000284607 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26571737..26571866 26863196 MeRIP-seq:(Medium) rs146624161 Functional Loss SNV dbSNP153 33..33 33 - - - 68703 RMVar_ID_68703 Human_SNP_ID_270793737 m1A Human chr6 + 26571744 26571744 26571744 ATGGGTGGTGAGAGAATCTTGAGCTTGAAGGAAAGACCACCCCCATTATGATACGGGAGTGTGTT ATGGGTGGTGAGAGAATCTTGAGCTTGAAGGATAGACCACCCCCATTATGATACGGGAGTGTGTT A T AL121936.1 Ensembl:ENSG00000284607 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:26571737..26571866 26863196 MeRIP-seq:(Medium) rs146624161 Functional Loss SNV dbSNP153 33..33 33 - - - 68704 RMVar_ID_68704 Human_SNP_ID_270793781 m1A Human chr6 + 26571825 26571825 26571825 TCAGCAAGATATTCATGGAAAGATAGGAGTAAAGGCCAAAGGGTAAGGTGGGAGAGGAAACCACA TCAGCAAGATATTCATGGAAAGATAGGAGTAATGGCCAAAGGGTAAGGTGGGAGAGGAAACCACA A T AL121936.1 Ensembl:ENSG00000284607 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26571722..26571868 26863196 MeRIP-seq:(Medium) rs973182284 Functional Loss SNV dbSNP153 33..33 33 - - - 68705 RMVar_ID_68705 Human_SNP_ID_270799536 m1A Human chr6 + 26594947 26594947 26594947 TTGAATGTGGTCATCCTTAGGTCGCTGGTTCGAATCCGGCTCGGAGGAGTTCCATTTTTAAAAGT TTGAATGTGGTCATCCTTAGGTCGCTGGTTCGTATCCGGCTCGGAGGAGTTCCATTTTTAAAAGT A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1188234690 Functional Loss SNV dbSNP153 33..33 33 - - - 68706 RMVar_ID_68706 Human_SNP_ID_270800082 m1A Human chr6 + 26597042 26597042 26597042 GCAACGGAGCAAGAGCCGCTGGAAGGGACAGAACAGACACTAGATGCGGAGGAGGAGCAGGAGGA GCAACGGAGCAAGAGCCGCTGGAAGGGACAGACCAGACACTAGATGCGGAGGAGGAGCAGGAGGA A C ABT1 Ensembl:ENSG00000146109 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:26596951..26597310;chr6:26596951..26597225 26863196 MeRIP-seq:(Medium) rs781995841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252298,Human_RBP_ID_3804403,Human_RBP_ID_9400114,Human_RBP_ID_22462489,Human_RBP_ID_24548668,Human_RBP_ID_26353501,Human_RBP_ID_27828338 68707 RMVar_ID_68707 Human_SNP_ID_270800110 m1A Human chr6 - 26597091 26597091 26597091 AATACCTGGCACTACCCGTTTCTTGCTGCCACAGGCCGCTTCTTCGGATTCCTCCTGCTCCTCCT AATACCTGGCACTACCCGTTTCTTGCTGCCACGGGCCGCTTCTTCGGATTCCTCCTGCTCCTCCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:26597006..26597095 26863410 MeRIP-seq:(Medium) rs1554144548 Functional Loss SNV dbSNP153 33..33 33 - - - 68708 RMVar_ID_68708 Human_SNP_ID_270800444 m1A Human chr6 + 26598042 26598042 26598042 GTGACAAGCGCATAGCCAAGCGCGTGGCGGCCAGTCTACACAACACGCCTATGGGTGCCCGCAGG GTGACAAGCGCATAGCCAAGCGCGTGGCGGCCGGTCTACACAACACGCCTATGGGTGCCCGCAGG A G ABT1 Ensembl:ENSG00000146109 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:26597991..26598092 32194978 MeRIP-seq:(Medium) rs782002448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_745847 Human_miRNA_ID_2087854,Human_miRNA_ID_2155368,Human_miRNA_ID_2158932 RMVar_hsa_circ_91601,RMVar_hsa_circ_237763 68709 RMVar_ID_68709 Human_SNP_ID_270810035 m1A Human chr6 - 26643007 26643003 26643007 GTGGGCCTCTTGGGCTATTGTGAAAGTAAGAAATAAGAGTGGTTTGGACTGGAATGTAACAACAG GTGGGCCTCTTGGGCTATTGTGAAAGTAAGAA____GAGTGGTTTGGACTGGAATGTAACAACAG CTTAT C ZNF322 Ensembl:ENSG00000181315 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26642970..26643054 26863196 MeRIP-seq:(Medium) rs1462273013 Functional Loss DEL dbSNP153 33..36 33 - - - 68710 RMVar_ID_68710 Human_SNP_ID_270813548 m1A Human chr6 - 26659701 26659701 26659701 CCTCTTCCCAGCCAGCTTGAAAGGGTTTGCGTAGCCGGCCTTGTGGGCCCTTGAAGCGCTCTGTT CCTCTTCCCAGCCAGCTTGAAAGGGTTTGCGTTGCCGGCCTTGTGGGCCCTTGAAGCGCTCTGTT T A ZNF322 Ensembl:ENSG00000181315 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26659602..26659713 26863196 MeRIP-seq:(Medium) rs948247356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659483,Human_RBP_ID_4903741 68711 RMVar_ID_68711 Human_SNP_ID_270821749 m1A Human chr6 + 26705413 26705413 26705413 AATTAGCTCAAGCGGTAGAGCGCTTGCTTAGCATGCAAGAGGTAGTGGGATCGATGCCCACATTC AATTAGCTCAAGCGGTAGAGCGCTTGCTTAGCCTGCAAGAGGTAGTGGGATCGATGCCCACATTC A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1554156364 Functional Loss SNV dbSNP153 33..33 33 - - - 68712 RMVar_ID_68712 Human_SNP_ID_270825765 m1A Human chr6 + 26743320 26743320 26743320 GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGAGCCTCAGAGAGGGCAGCTTTTGCAAGGAAAGC GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGGGCCTCAGAGAGGGCAGCTTTTGCAAGGAAAGC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs546327726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26751487 68713 RMVar_ID_68713 Human_SNP_ID_270829525 m1A Human chr6 + 26756610 26756610 26756610 GTGGTGCTAATAACGCTAAGGTCGCGGGTTCGATCCCCGTACTGGCCAGACGTGACTTTTTAATG GTGGTGCTAATAACGCTAAGGTCGCGGGTTCGGTCCCCGTACTGGCCAGACGTGACTTTTTAATG A G HSALNG0050851-001 RNACentral:URS0000EC1E24 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1291960606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5305669,Human_RBP_ID_17711619,Human_RBP_ID_18539893,Human_RBP_ID_24437445 68714 RMVar_ID_68714 Human_SNP_ID_270874735 m1A Human chr6 - 27020317 27020317 27020317 GAGCACCCAGTTTCTACTTCCGGTCACTCCTTACACAGCCTACACAGGAACATCCGGCGTGTTTG GAGCACCCAGTTTCTACTTCCGGTCACTCCTTTCACAGCCTACACAGGAACATCCGGCGTGTTTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27020268..27020390 26863196 MeRIP-seq:(Medium) rs1419217823 Functional Loss SNV dbSNP153 33..33 33 - - - 68715 RMVar_ID_68715 Human_SNP_ID_270890038 m1A Human chr6 + 27091797 27091785 27091798 TTCTCGCTTCGGGTGTGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCACTTCATTTTCGCCCA TTCTCGCTTCGGGTGTGAGAG_____________ATCCCGGACGAGCCCACTTCATTTTCGCCCA GGTCCCGGGTTCAA G lnc-HIST1H2AG-4,tRNA-Pro-CGG-2-1 RNACentral:URS00008BC581,RNACentral:URS00006744D5 lincRNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs762470380 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_1326511,Human_RBP_ID_1394745,Human_RBP_ID_1669187,Human_RBP_ID_5216209,Human_RBP_ID_5268348,Human_RBP_ID_5477825,Human_RBP_ID_7586538,Human_RBP_ID_8269878,Human_RBP_ID_8640355,Human_RBP_ID_8899259,Human_RBP_ID_15771439,Human_RBP_ID_18211354,Human_RBP_ID_18860941,Human_RBP_ID_21315786,Human_RBP_ID_22830529,Human_RBP_ID_23138145,Human_RBP_ID_24153827,Human_RBP_ID_24435469,Human_RBP_ID_27094026,Human_RBP_ID_27344227,Human_RBP_ID_27522145 68716 RMVar_ID_68716 Human_SNP_ID_270890053 m1A Human chr6 + 27091797 27091797 27091797 TTCTCGCTTCGGGTGTGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCACTTCATTTTCGCCCA TTCTCGCTTCGGGTGTGAGAGGTCCCGGGTTCGAATCCCGGACGAGCCCACTTCATTTTCGCCCA A G lnc-HIST1H2AG-4,tRNA-Pro-CGG-2-1 RNACentral:URS00008BC581,RNACentral:URS00006744D5 lincRNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs772646860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326511,Human_RBP_ID_1394745,Human_RBP_ID_1669187,Human_RBP_ID_5216209,Human_RBP_ID_5268348,Human_RBP_ID_5477825,Human_RBP_ID_7586538,Human_RBP_ID_8269878,Human_RBP_ID_8640355,Human_RBP_ID_8899259,Human_RBP_ID_15771439,Human_RBP_ID_18211354,Human_RBP_ID_18860941,Human_RBP_ID_21315786,Human_RBP_ID_22830529,Human_RBP_ID_23138145,Human_RBP_ID_24153827,Human_RBP_ID_24435469,Human_RBP_ID_27094026,Human_RBP_ID_27344227,Human_RBP_ID_27522145 68717 RMVar_ID_68717 Human_SNP_ID_270899621 m1A Human chr6 - 27132680 27132680 27132680 GGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGACGGCAAGAAGCGCAAGCGCAGCCGCA GGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAGGAAAGACGGCAAGAAGCGCAAGCGCAGCCGCA T C H2BC11 Ensembl:ENSG00000124635 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:27132581..27132748 26863196 MeRIP-seq:(Medium) rs762559532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270788,Human_RBP_ID_659532,Human_RBP_ID_1669212,Human_RBP_ID_2016950,Human_RBP_ID_3804535,Human_RBP_ID_4876988,Human_RBP_ID_5450925,Human_RBP_ID_8640380,Human_RBP_ID_9336008,Human_RBP_ID_15771666,Human_RBP_ID_18210949,Human_RBP_ID_22460495,Human_RBP_ID_22832646,Human_RBP_ID_23138154,Human_RBP_ID_26714299,Human_RBP_ID_27094035,Human_RBP_ID_27344235 RMVar_hsa_circ_89811,RMVar_hsa_circ_112395,RMVar_hsa_circ_237767,RMVar_hsa_circ_237768 68718 RMVar_ID_68718 Human_SNP_ID_270899624 m1A Human chr6 - 27132683 27132683 27132683 AAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGACGGCAAGAAGCGCAAGCGCAGCC AAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCGGAAGAAAGACGGCAAGAAGCGCAAGCGCAGCC T C H2BC11 Ensembl:ENSG00000124635 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:27132632..27132716 26863196 MeRIP-seq:(Medium) rs1369577809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659532,Human_RBP_ID_1669212,Human_RBP_ID_2016950,Human_RBP_ID_3804535,Human_RBP_ID_4876988,Human_RBP_ID_5450926,Human_RBP_ID_9336008,Human_RBP_ID_15771666,Human_RBP_ID_22460495,Human_RBP_ID_23138154 RMVar_hsa_circ_89811,RMVar_hsa_circ_112395,RMVar_hsa_circ_237767,RMVar_hsa_circ_237768 68719 RMVar_ID_68719 Human_SNP_ID_270899633 m1A Human chr6 - 27132690 27132690 27132690 CCCCGAAAAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGACGGCAAGAAGCGCAAG CCCCGAAAAAGGGCTCCAAGAAGGCGGTGACTGAGGCGCAGAAGAAAGACGGCAAGAAGCGCAAG T C H2BC11 Ensembl:ENSG00000124635 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27132524..27132750 26863196 MeRIP-seq:(Medium) rs935230437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80041,Human_RBP_ID_659532,Human_RBP_ID_1669212,Human_RBP_ID_2016950,Human_RBP_ID_3804535,Human_RBP_ID_4876988,Human_RBP_ID_5450926,Human_RBP_ID_9336008,Human_RBP_ID_15771666,Human_RBP_ID_22460495,Human_RBP_ID_22830546,Human_RBP_ID_23138154,Human_RBP_ID_25992954,Human_RBP_ID_27568235 RMVar_hsa_circ_89811,RMVar_hsa_circ_112395,RMVar_hsa_circ_237767,RMVar_hsa_circ_237768 68720 RMVar_ID_68720 Human_SNP_ID_270899644 m1A Human chr6 - 27132701 27132701 27132701 GTCTGCTCCCGCCCCGAAAAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGACGGCA GTCTGCTCCCGCCCCGAAAAAGGGCTCCAAGATGGCGGTGACTAAGGCGCAGAAGAAAGACGGCA T A H2BC11 Ensembl:ENSG00000124635 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27132676..27132700 26863196 MeRIP-seq:(Medium) rs369110288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80041,Human_RBP_ID_659532,Human_RBP_ID_1669212,Human_RBP_ID_2016950,Human_RBP_ID_3804535,Human_RBP_ID_4876988,Human_RBP_ID_5450927,Human_RBP_ID_5478666,Human_RBP_ID_8640381,Human_RBP_ID_9336008,Human_RBP_ID_15771666,Human_RBP_ID_22104740,Human_RBP_ID_22309507,Human_RBP_ID_22461705,Human_RBP_ID_22830547,Human_RBP_ID_26045685,Human_RBP_ID_26540947,Human_RBP_ID_27094036,Human_RBP_ID_27344236,Human_RBP_ID_27522156 RMVar_hsa_circ_89811,RMVar_hsa_circ_112395,RMVar_hsa_circ_237767,RMVar_hsa_circ_237768 68721 RMVar_ID_68721 Human_SNP_ID_270899645 m1A Human chr6 - 27132701 27132701 27132701 GTCTGCTCCCGCCCCGAAAAAGGGCTCCAAGAAGGCGGTGACTAAGGCGCAGAAGAAAGACGGCA GTCTGCTCCCGCCCCGAAAAAGGGCTCCAAGAGGGCGGTGACTAAGGCGCAGAAGAAAGACGGCA T C H2BC11 Ensembl:ENSG00000124635 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27132676..27132700 26863196 MeRIP-seq:(Medium) rs369110288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80041,Human_RBP_ID_659532,Human_RBP_ID_1669212,Human_RBP_ID_2016950,Human_RBP_ID_3804535,Human_RBP_ID_4876988,Human_RBP_ID_5450927,Human_RBP_ID_5478666,Human_RBP_ID_8640381,Human_RBP_ID_9336008,Human_RBP_ID_15771666,Human_RBP_ID_22104740,Human_RBP_ID_22309507,Human_RBP_ID_22461705,Human_RBP_ID_22830547,Human_RBP_ID_26045685,Human_RBP_ID_26540947,Human_RBP_ID_27094036,Human_RBP_ID_27344236,Human_RBP_ID_27522156 RMVar_hsa_circ_89811,RMVar_hsa_circ_112395,RMVar_hsa_circ_237767,RMVar_hsa_circ_237768 68722 RMVar_ID_68722 Human_SNP_ID_270899921 m1A Human chr6 - 27133075 27133075 27133075 GCGGGCTTTGCCTCCCTGCTTGCCACGTCCAGACATAGCGAGCGCAACTCACTACGAGCAACCAC GCGGGCTTTGCCTCCCTGCTTGCCACGTCCAGGCATAGCGAGCGCAACTCACTACGAGCAACCAC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27133051..27133075 26863196 MeRIP-seq:(Medium) rs755987256 Functional Loss SNV dbSNP153 33..33 33 - - - 68723 RMVar_ID_68723 Human_SNP_ID_270899922 m1A Human chr6 - 27133075 27133075 27133075 GCGGGCTTTGCCTCCCTGCTTGCCACGTCCAGACATAGCGAGCGCAACTCACTACGAGCAACCAC GCGGGCTTTGCCTCCCTGCTTGCCACGTCCAGCCATAGCGAGCGCAACTCACTACGAGCAACCAC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27133051..27133075 26863196 MeRIP-seq:(Medium) rs755987256 Functional Loss SNV dbSNP153 33..33 33 - - - 68724 RMVar_ID_68724 Human_SNP_ID_270899991 m1A Human chr6 - 27133147 27133147 27133147 GCGGAGCAGGCGGTGCACTCGGCCCACGGGGAACTGGAGACCGGCCCTAGAAGAGCGAGTCTTGG GCGGAGCAGGCGGTGCACTCGGCCCACGGGGATCTGGAGACCGGCCCTAGAAGAGCGAGTCTTGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27133102..27133244 26863196 MeRIP-seq:(Medium) rs995051731 Functional Loss SNV dbSNP153 33..33 33 - - - 68725 RMVar_ID_68725 Human_SNP_ID_270899992 m1A Human chr6 - 27133147 27133147 27133147 GCGGAGCAGGCGGTGCACTCGGCCCACGGGGAACTGGAGACCGGCCCTAGAAGAGCGAGTCTTGG GCGGAGCAGGCGGTGCACTCGGCCCACGGGGAGCTGGAGACCGGCCCTAGAAGAGCGAGTCTTGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27133102..27133244 26863196 MeRIP-seq:(Medium) rs995051731 Functional Loss SNV dbSNP153 33..33 33 - - - 68726 RMVar_ID_68726 Human_SNP_ID_270901670 m1A Human chr6 + 27139325 27139325 27139325 CTCTGACCACTTGATAATGTCAGGACGCGGCAAAGGAGGTAAGGGCCTGGGGAAAGGGGGTGCCA CTCTGACCACTTGATAATGTCAGGACGCGGCAGAGGAGGTAAGGGCCTGGGGAAAGGGGGTGCCA A G H4C9 Ensembl:ENSG00000276180 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27139276..27139325 26863196 MeRIP-seq:(Medium) rs750256756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903744,Human_RBP_ID_5327080,Human_RBP_ID_9336519,Human_RBP_ID_22105702,Human_RBP_ID_22460501,Human_RBP_ID_22706265,Human_RBP_ID_23214696 RMVar_hsa_circ_122237,RMVar_hsa_circ_237769 68727 RMVar_ID_68727 Human_SNP_ID_270903565 m1A Human chr6 - 27145458 27145458 27145458 GATTAGAGGCTAGAATGACTATGCCGGTGATGAGCAGTGTGAAACTTTTTTGGAAGAACCAAGTG GATTAGAGGCTAGAATGACTATGCCGGTGATGGGCAGTGTGAAACTTTTTTGGAAGAACCAAGTG T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27145456..27145609 26863196 MeRIP-seq:(Medium) rs1464857050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3001250,Human_RBP_ID_15771753,Human_RBP_ID_24153910 RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 68728 RMVar_ID_68728 Human_SNP_ID_270904038 m1A Human chr6 - 27146583 27146583 27146583 ATCATGAACTCCTTCGTCAACGACATCTTCGAACGCATCGCGGGTGAGGCTTCCCGCCTGGCGCA ATCATGAACTCCTTCGTCAACGACATCTTCGAGCGCATCGCGGGTGAGGCTTCCCGCCTGGCGCA T C H2BC12 Ensembl:ENSG00000197903 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27146535..27146615 26863196 MeRIP-seq:(Medium) rs758323873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81124,Human_RBP_ID_251758,Human_RBP_ID_659588,Human_RBP_ID_1046201,Human_RBP_ID_1669249,Human_RBP_ID_2016970,Human_RBP_ID_3804563,Human_RBP_ID_7586728,Human_RBP_ID_8640412,Human_RBP_ID_8899282,Human_RBP_ID_15771770,Human_RBP_ID_18195347,Human_RBP_ID_18369608,Human_RBP_ID_18449973,Human_RBP_ID_18538989,Human_RBP_ID_18860987,Human_RBP_ID_22460504,Human_RBP_ID_22513809,Human_RBP_ID_26353503,Human_RBP_ID_26828046,Human_RBP_ID_27522185 Human_miRNA_ID_3003569,Human_miRNA_ID_3003570 RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 68729 RMVar_ID_68729 Human_SNP_ID_270904537 m1A Human chr6 - 27147220 27147220 27147220 CGGCATAATTACCCTTGCGGAGCAGGCGGTGCACTCGGCCCACGGGGAACTGAAGCCCAGCCCGA CGGCATAATTACCCTTGCGGAGCAGGCGGTGCCCTCGGCCCACGGGGAACTGAAGCCCAGCCCGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27147169..27147310 26863196 MeRIP-seq:(Medium) rs745589618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_237770,RMVar_hsa_circ_77092,RMVar_hsa_circ_237773 68730 RMVar_ID_68730 Human_SNP_ID_270907543 m1A Human chr6 - 27158243 27158243 27158243 CTCCAGTATGTTGAAAAATTGAGGCGACGTCAAGGTACTGCTCAGTACGTTGAGAAATTGAGGCG CTCCAGTATGTTGAAAAATTGAGGCGACGTCACGGTACTGCTCAGTACGTTGAGAAATTGAGGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:27158194..27158314 26863196 MeRIP-seq:(Medium) rs1339722770 Functional Loss SNV dbSNP153 33..33 33 - - - 68731 RMVar_ID_68731 Human_SNP_ID_270919411 m1A Human chr6 - 27206103 27206103 27206103 GTTCGCCTCACACGCGAAAGGTCCCCGGTTTGAAACCAGGCGGAAACATTCTTTACTCGTTTGGT GTTCGCCTCACACGCGAAAGGTCCCCGGTTTGCAACCAGGCGGAAACATTCTTTACTCGTTTGGT T G tRNA-Val-CAC-6-1 RNACentral:URS0000732DD4 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1244924385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669283,Human_RBP_ID_4910309,Human_RBP_ID_5276990,Human_RBP_ID_8640439,Human_RBP_ID_22830584,Human_RBP_ID_23138180,Human_RBP_ID_27094072,Human_RBP_ID_27344274 68732 RMVar_ID_68732 Human_SNP_ID_270926227 m1A Human chr6 - 27230432 27230432 27230432 ACTTTGCGTGTAAACGCTTCAAATAATAACGAAGGTTATTAAACAATATTCTGCCCAACACTACT ACTTTGCGTGTAAACGCTTCAAATAATAACGATGGTTATTAAACAATATTCTGCCCAACACTACT T A lnc-POM121L2-3 RNACentral:URS0000D5BC91 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr6:27230401..27230475;chr6:27230401..27230450 26863196 MeRIP-seq:(Medium) rs1163371482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216750,Human_RBP_ID_1326536,Human_RBP_ID_1669300,Human_RBP_ID_2016999,Human_RBP_ID_3001263,Human_RBP_ID_3804590,Human_RBP_ID_8640453,Human_RBP_ID_18861034,Human_RBP_ID_21316029,Human_RBP_ID_23138203,Human_RBP_ID_24511958 68733 RMVar_ID_68733 Human_SNP_ID_270926295 m1A Human chr6 + 27230497 27230497 27230497 GAGAAGGTTGTCATATTAGTTTTTATGTAAGCATACCTGGCTTCCAACTCTGCGGCAGAAACCGC GAGAAGGTTGTCATATTAGTTTTTATGTAAGCGTACCTGGCTTCCAACTCTGCGGCAGAAACCGC A G lnc-PRSS16-1 RNACentral:URS00008B8BBF lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:27230449..27230538 26863196 MeRIP-seq:(Medium) rs1419275823 Functional Loss SNV dbSNP153 33..33 33 - - - 68734 RMVar_ID_68734 Human_SNP_ID_270926334 m1A Human chr6 + 27230539 27230539 27230539 TCCAACTCTGCGGCAGAAACCGCAAACGTCAAAGTACACACCAACGCTTACCGGGAGTGGGGCTC TCCAACTCTGCGGCAGAAACCGCAAACGTCAAGGTACACACCAACGCTTACCGGGAGTGGGGCTC A G lnc-PRSS16-1 RNACentral:URS00008B8BBF lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr6:27230501..27230600;chr6:27230422..27230554 26863196 MeRIP-seq:(Medium) rs953871300 Functional Loss SNV dbSNP153 33..33 33 - - - 68735 RMVar_ID_68735 Human_SNP_ID_270926336 m1A Human chr6 - 27230541 27230541 27230541 TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTACTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTTCTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG T A lnc-POM121L2-3 RNACentral:URS0000D5BC91 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:27230401..27230575 26863196 MeRIP-seq:(Medium) rs9468014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270797,Human_RBP_ID_659606,Human_RBP_ID_1216752,Human_RBP_ID_1669302,Human_RBP_ID_2016999,Human_RBP_ID_3001264,Human_RBP_ID_3804591,Human_RBP_ID_4877076,Human_RBP_ID_5216223,Human_RBP_ID_8269898,Human_RBP_ID_8640455,Human_RBP_ID_15771837,Human_RBP_ID_17198361,Human_RBP_ID_18861038,Human_RBP_ID_21316035,Human_RBP_ID_22830599,Human_RBP_ID_23138205,Human_RBP_ID_24153948,Human_RBP_ID_24511962,Human_RBP_ID_26534682,Human_RBP_ID_26714315,Human_RBP_ID_27094081,Human_RBP_ID_27160964,Human_RBP_ID_27344284 GWAS_ID_8227,GWAS_ID_8228,GWAS_ID_8229,GWAS_ID_8230 68736 RMVar_ID_68736 Human_SNP_ID_270926337 m1A Human chr6 - 27230541 27230541 27230541 TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTACTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTGCTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG T C lnc-POM121L2-3 RNACentral:URS0000D5BC91 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:27230401..27230575 26863196 MeRIP-seq:(Medium) rs9468014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270797,Human_RBP_ID_659606,Human_RBP_ID_1216752,Human_RBP_ID_1669302,Human_RBP_ID_2016999,Human_RBP_ID_3001264,Human_RBP_ID_3804591,Human_RBP_ID_4877076,Human_RBP_ID_5216223,Human_RBP_ID_8269898,Human_RBP_ID_8640455,Human_RBP_ID_15771837,Human_RBP_ID_17198361,Human_RBP_ID_18861038,Human_RBP_ID_21316035,Human_RBP_ID_22830599,Human_RBP_ID_23138205,Human_RBP_ID_24153948,Human_RBP_ID_24511962,Human_RBP_ID_26534682,Human_RBP_ID_26714315,Human_RBP_ID_27094081,Human_RBP_ID_27160964,Human_RBP_ID_27344284 GWAS_ID_8227,GWAS_ID_8228,GWAS_ID_8229,GWAS_ID_8230 68737 RMVar_ID_68737 Human_SNP_ID_270926354 m1A Human chr6 + 27230556 27230556 27230556 AACCGCAAACGTCAAAGTACACACCAACGCTTACCGGGAGTGGGGCTCGAACCCACGCGGACACC AACCGCAAACGTCAAAGTACACACCAACGCTTTCCGGGAGTGGGGCTCGAACCCACGCGGACACC A T lnc-PRSS16-1 RNACentral:URS00008B8BBF lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27230526..27230575 26863196 MeRIP-seq:(Medium) rs76456228 Functional Loss SNV dbSNP153 33..33 33 - - - 68738 RMVar_ID_68738 Human_SNP_ID_270926374 m1A Human chr6 - 27230570 27230570 27230570 AGATCCAATGGACAGGTGTCCGCGTGGGTTCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTACTT AGATCCAATGGACAGGTGTCCGCGTGGGTTCGGGCCCCACTCCCGGTAAGCGTTGGTGTGTACTT T C tRNA-Leu-TAA-4-1,piR-53944,lnc-POM121L2-3 RNACentral:URS0000716955,RNACentral:URS0000420317,RNACentral:URS0000D5BC91 tRNA,piRNA,lincRNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1247455946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659606,Human_RBP_ID_1394759,Human_RBP_ID_1669302,Human_RBP_ID_2016999,Human_RBP_ID_3804591,Human_RBP_ID_4910318,Human_RBP_ID_5276666,Human_RBP_ID_7586794,Human_RBP_ID_8269898,Human_RBP_ID_8640455,Human_RBP_ID_8899302,Human_RBP_ID_18861039,Human_RBP_ID_21316035,Human_RBP_ID_22830599,Human_RBP_ID_23059175,Human_RBP_ID_23138205,Human_RBP_ID_24153948,Human_RBP_ID_26534682,Human_RBP_ID_27094081,Human_RBP_ID_27160966,Human_RBP_ID_27344285 68739 RMVar_ID_68739 Human_SNP_ID_270928557 m1A Human chr6 - 27237545 27237545 27237545 CGGGCCACGAGGGTTCTCACCTTCTCTCTCCGATTTTGCCGCAGTCACTTCACATCCAGCTATAC CGGGCCACGAGGGTTCTCACCTTCTCTCTCCGTTTTTGCCGCAGTCACTTCACATCCAGCTATAC T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:27237479..27237625 26863410 MeRIP-seq:(Medium) rs1012042791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216759,Human_RBP_ID_1326537,Human_RBP_ID_1394760,Human_RBP_ID_1679020,Human_RBP_ID_2017006,Human_RBP_ID_3804594,Human_RBP_ID_5276667,Human_RBP_ID_5477852,Human_RBP_ID_7586798,Human_RBP_ID_8640460,Human_RBP_ID_18861047,Human_RBP_ID_21316042,Human_RBP_ID_22102460,Human_RBP_ID_22832663,Human_RBP_ID_23138216,Human_RBP_ID_27161297,Human_RBP_ID_27344291 68740 RMVar_ID_68740 Human_SNP_ID_270928558 m1A Human chr6 - 27237545 27237545 27237545 CGGGCCACGAGGGTTCTCACCTTCTCTCTCCGATTTTGCCGCAGTCACTTCACATCCAGCTATAC CGGGCCACGAGGGTTCTCACCTTCTCTCTCCGGTTTTGCCGCAGTCACTTCACATCCAGCTATAC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:27237479..27237625 26863410 MeRIP-seq:(Medium) rs1012042791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216759,Human_RBP_ID_1326537,Human_RBP_ID_1394760,Human_RBP_ID_1679020,Human_RBP_ID_2017006,Human_RBP_ID_3804594,Human_RBP_ID_5276667,Human_RBP_ID_5477852,Human_RBP_ID_7586798,Human_RBP_ID_8640460,Human_RBP_ID_18861047,Human_RBP_ID_21316042,Human_RBP_ID_22102460,Human_RBP_ID_22832663,Human_RBP_ID_23138216,Human_RBP_ID_27161297,Human_RBP_ID_27344291 68741 RMVar_ID_68741 Human_SNP_ID_270928580 m1A Human chr6 - 27237559 27237559 27237559 GTTCGATCCCCGTACGGGCCACGAGGGTTCTCACCTTCTCTCTCCGATTTTGCCGCAGTCACTTC GTTCGATCCCCGTACGGGCCACGAGGGTTCTCGCCTTCTCTCTCCGATTTTGCCGCAGTCACTTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:27237457..27237569 26863410 MeRIP-seq:(Medium) rs569964636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046217,Human_RBP_ID_1216759,Human_RBP_ID_1326537,Human_RBP_ID_1394760,Human_RBP_ID_1679020,Human_RBP_ID_2017006,Human_RBP_ID_3001265,Human_RBP_ID_3804594,Human_RBP_ID_5276667,Human_RBP_ID_5477852,Human_RBP_ID_7586798,Human_RBP_ID_8640460,Human_RBP_ID_18861047,Human_RBP_ID_21316042,Human_RBP_ID_22832663,Human_RBP_ID_23138216,Human_RBP_ID_26540972,Human_RBP_ID_27161297,Human_RBP_ID_27344291 68742 RMVar_ID_68742 Human_SNP_ID_270931861 m1A Human chr6 - 27251256 27251256 27251256 CTCGGACTAGGCCCCACCTCCTACCTCCAGGGACCCGCCGATCGCGGTGCTCATTAGGCTTCGGG CTCGGACTAGGCCCCACCTCCTACCTCCAGGGCCCCGCCGATCGCGGTGCTCATTAGGCTTCGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27251208..27251546 26863196 MeRIP-seq:(Medium) rs773318984 Functional Loss SNV dbSNP153 33..33 33 - - - 68743 RMVar_ID_68743 Human_SNP_ID_270931865 m1A Human chr6 - 27251266 27251266 27251266 CCCAGTCCCCCTCGGACTAGGCCCCACCTCCTACCTCCAGGGACCCGCCGATCGCGGTGCTCATT CCCAGTCCCCCTCGGACTAGGCCCCACCTCCTCCCTCCAGGGACCCGCCGATCGCGGTGCTCATT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27251258..27251479 26863196 MeRIP-seq:(Medium) rs878934959 Functional Loss SNV dbSNP153 33..33 33 - - - 68744 RMVar_ID_68744 Human_SNP_ID_270932061 m1A Human chr6 - 27251806 27251806 27251806 AGCTCCGTCCGCAATGCTGCTTGAGCCGCCCCACCCGAGCGCAGCCGCCGCTCCACTTCAGCGAA AGCTCCGTCCGCAATGCTGCTTGAGCCGCCCCCCCCGAGCGCAGCCGCCGCTCCACTTCAGCGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27251557..27251931 26863196 MeRIP-seq:(Medium) rs578258212 Functional Loss SNV dbSNP153 33..33 33 - - - 68745 RMVar_ID_68745 Human_SNP_ID_270939482 m1A Human chr6 + 27280235 27280235 27280235 GTGCGGGGGTGCAATTCTAAAAACGTGCACTGAGAAATTCAGCTAAGGATTCCTCAAAAATACAG GTGCGGGGGTGCAATTCTAAAAACGTGCACTGGGAAATTCAGCTAAGGATTCCTCAAAAATACAG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27280187..27280314 26863196 MeRIP-seq:(Medium) rs558269416 Functional Loss SNV dbSNP153 33..33 33 - - - 68746 RMVar_ID_68746 Human_SNP_ID_270943650 m1A Human chr6 - 27295491 27295491 27295491 CTGCAGAGGACTAAATCCAAGGTTCCACCGAGATTTGAACTCGGATTACCGGATTCAGAGTCCAG CTGCAGAGGACTAAATCCAAGGTTCCACCGAGGTTTGAACTCGGATTACCGGATTCAGAGTCCAG T C POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:27295448..27295567;chr6:27295448..27295571;chr6:27295448..27295580 26863196 MeRIP-seq:(Medium) rs528508772 Functional Loss SNV dbSNP153 33..33 33 - - - 68747 RMVar_ID_68747 Human_SNP_ID_270943654 m1A Human chr6 - 27295497 27295497 27295497 ATTTGACTGCAGAGGACTAAATCCAAGGTTCCACCGAGATTTGAACTCGGATTACCGGATTCAGA ATTTGACTGCAGAGGACTAAATCCAAGGTTCCGCCGAGATTTGAACTCGGATTACCGGATTCAGA T C POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27295458..27295570 26863196 MeRIP-seq:(Medium) rs953027039 Functional Loss SNV dbSNP153 33..33 33 - - - 68748 RMVar_ID_68748 Human_SNP_ID_270943665 m1A Human chr6 - 27295509 27295509 27295509 GAGACGATGGGGATTTGACTGCAGAGGACTAAATCCAAGGTTCCACCGAGATTTGAACTCGGATT GAGACGATGGGGATTTGACTGCAGAGGACTAATTCCAAGGTTCCACCGAGATTTGAACTCGGATT T A POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27295460..27295556 26863196 MeRIP-seq:(Medium) rs966689368 Functional Loss SNV dbSNP153 33..33 33 - - - 68749 RMVar_ID_68749 Human_SNP_ID_270943666 m1A Human chr6 - 27295509 27295509 27295509 GAGACGATGGGGATTTGACTGCAGAGGACTAAATCCAAGGTTCCACCGAGATTTGAACTCGGATT GAGACGATGGGGATTTGACTGCAGAGGACTAAGTCCAAGGTTCCACCGAGATTTGAACTCGGATT T C POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27295460..27295556 26863196 MeRIP-seq:(Medium) rs966689368 Functional Loss SNV dbSNP153 33..33 33 - - - 68750 RMVar_ID_68750 Human_SNP_ID_270944377 m1A Human chr6 + 27298062 27298062 27298062 CTAATCCATTGTGCTCTGCACGCGTGGGTTCGAATCCCACCTTCGTCGACCGTTTTCTTTAAGAG CTAATCCATTGTGCTCTGCACGCGTGGGTTCGGATCCCACCTTCGTCGACCGTTTTCTTTAAGAG A G POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs562283660 Functional Loss SNV dbSNP153 33..33 33 - - - 68751 RMVar_ID_68751 Human_SNP_ID_270945942 m1A Human chr6 - 27303813 27303813 27303813 CGGAAGCGTGCTGGGCCCGTAACCCAGAGGTCAATGGATCGAAGCCATCCTTGGCTAGGGTGTTT CGGAAGCGTGCTGGGCCCGTAACCCAGAGGTCTATGGATCGAAGCCATCCTTGGCTAGGGTGTTT T A POM121L2 Ensembl:ENSG00000158553 Protein coding intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs989984886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78771,Human_RBP_ID_659633,Human_RBP_ID_1669334,Human_RBP_ID_2017023,Human_RBP_ID_5219015,Human_RBP_ID_5268962,Human_RBP_ID_7586828,Human_RBP_ID_8640488,Human_RBP_ID_15771898,Human_RBP_ID_17161379,Human_RBP_ID_18539889,Human_RBP_ID_18861084,Human_RBP_ID_22830621,Human_RBP_ID_23138261,Human_RBP_ID_24554787,Human_RBP_ID_24562885 68752 RMVar_ID_68752 Human_SNP_ID_270952794 m1A Human chr6 + 27332978 27332978 27332978 GTTTTTGTTTTTTGCGTGTCGATTTAGCTGTAAAACTCATAGCAGAGGATGGTTTCGATCCATCG GTTTTTGTTTTTTGCGTGTCGATTTAGCTGTAGAACTCATAGCAGAGGATGGTTTCGATCCATCG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:27332880..27332979 26863410 MeRIP-seq:(Medium) rs773348995 Functional Loss SNV dbSNP153 33..33 33 - - - 68753 RMVar_ID_68753 Human_SNP_ID_270952839 m1A Human chr6 - 27333004 27333004 27333004 GCGTGCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTATGAGTTTTACAGC GCGTGCTGGGCCCATAACCCAGAGGTCGATGGTTCGAAACCATCCTCTGCTATGAGTTTTACAGC T A tRNA-iMet-CAT-1-1,TRX-CAT1-1,piR-33543 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC,RNACentral:URS000031CF48 tRNA,tRNA,piRNA exon,exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:27332943..27333028 26863410 MeRIP-seq:(Medium) rs1197904614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659635,Human_RBP_ID_1669339,Human_RBP_ID_18211186,Human_RBP_ID_21316164,Human_RBP_ID_22830623,Human_RBP_ID_23138267,Human_RBP_ID_26751470 68754 RMVar_ID_68754 Human_SNP_ID_270953491 m1A Human chr6 - 27335005 27335005 27335005 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTCCAGGCGCTAAAAATGCAACTTTT ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAGGTCCCTGTCCAGGCGCTAAAAATGCAACTTTT T C tRNA-Lys-TTT-6-1 RNACentral:URS000071C635 tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1319886889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216782,Human_RBP_ID_1326548,Human_RBP_ID_1394776,Human_RBP_ID_1669342,Human_RBP_ID_2017025,Human_RBP_ID_3804620,Human_RBP_ID_5269062,Human_RBP_ID_5277016,Human_RBP_ID_5305665,Human_RBP_ID_7586835,Human_RBP_ID_8269911,Human_RBP_ID_8640492,Human_RBP_ID_8899316,Human_RBP_ID_15771908,Human_RBP_ID_17065021,Human_RBP_ID_17198363,Human_RBP_ID_17710248,Human_RBP_ID_18071812,Human_RBP_ID_18449985,Human_RBP_ID_18861093,Human_RBP_ID_22102466,Human_RBP_ID_23138270,Human_RBP_ID_24437438,Human_RBP_ID_24513724,Human_RBP_ID_27344312 68755 RMVar_ID_68755 Human_SNP_ID_270984592 m1A Human chr6 + 27478948 27478948 27478948 CAGCGAGGAAATAGGATCTCACATTTGCTTTCAGTTTGGGAGTAAAGAAACTCGTGATAGAGCCT CAGCGAGGAAATAGGATCTCACATTTGCTTTCGGTTTGGGAGTAAAGAAACTCGTGATAGAGCCT A G AL021918.5 Ensembl:ENSG00000286652 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27478903..27479013 26863196 MeRIP-seq:(Medium) rs187412655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2017072,Human_RBP_ID_15772387,Human_RBP_ID_23059188,Human_RBP_ID_23138279 68756 RMVar_ID_68756 Human_SNP_ID_270984818 m1A Human chr6 + 27479682 27479682 27479682 TAAGAGCTCCATTTTCACGTCAATTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG TAAGAGCTCCATTTTCACGTCAATTCCTCGTTTGTATAGTGGTGAGTATCCCCGCCTGTCACGCG A T AL021918.5 Ensembl:ENSG00000286652 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1561847781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326556,Human_RBP_ID_1394784,Human_RBP_ID_1669378,Human_RBP_ID_2017073,Human_RBP_ID_8640525,Human_RBP_ID_8899326,Human_RBP_ID_18211161,Human_RBP_ID_18861152,Human_RBP_ID_23111957,Human_RBP_ID_23138286,Human_RBP_ID_24154209 68757 RMVar_ID_68757 Human_SNP_ID_270984859 m1A Human chr6 + 27479730 27479725 27479730 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGAGGCTTAAACTTTTTT TCCCCGCCTGTCACGCGGGAGACCGGGG_____TTCCCCGACGGGGAGGAGGCTTAAACTTTTTT GTTCGA G AL021918.5 Ensembl:ENSG00000286652 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1196671948 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_284904,Human_RBP_ID_659726,Human_RBP_ID_1679033,Human_RBP_ID_3804697,Human_RBP_ID_5276682,Human_RBP_ID_7587111,Human_RBP_ID_8640527,Human_RBP_ID_9192998,Human_RBP_ID_18071907,Human_RBP_ID_18449993,Human_RBP_ID_18861154,Human_RBP_ID_21316612,Human_RBP_ID_22830631,Human_RBP_ID_23138288,Human_RBP_ID_23314599,Human_RBP_ID_24154212,Human_RBP_ID_26751536 68758 RMVar_ID_68758 Human_SNP_ID_270984869 m1A Human chr6 + 27479730 27479730 27479730 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGAGGCTTAAACTTTTTT TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGGAGGCTTAAACTTTTTT A G AL021918.5 Ensembl:ENSG00000286652 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1317192444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284904,Human_RBP_ID_659726,Human_RBP_ID_1679033,Human_RBP_ID_3804697,Human_RBP_ID_5276682,Human_RBP_ID_7587111,Human_RBP_ID_8640527,Human_RBP_ID_9192998,Human_RBP_ID_18071907,Human_RBP_ID_18449993,Human_RBP_ID_18861154,Human_RBP_ID_21316612,Human_RBP_ID_22830631,Human_RBP_ID_23138288,Human_RBP_ID_23314599,Human_RBP_ID_24154212,Human_RBP_ID_26751536 68759 RMVar_ID_68759 Human_SNP_ID_270990550 m1A Human chr6 - 27503140 27503140 27503140 TAAATTTCTTTCTTCTAAATTTTCTGTTGTTAATTATCTAAAACCTCGAACTCGTAGTCGGCAGG TAAATTTCTTTCTTCTAAATTTTCTGTTGTTAGTTATCTAAAACCTCGAACTCGTAGTCGGCAGG T C AL021918.3 Ensembl:ENSG00000285703 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27503100..27503230 26863196 MeRIP-seq:(Medium) rs1332802036 Functional Loss SNV dbSNP153 33..33 33 - - - 68760 RMVar_ID_68760 Human_SNP_ID_270990776 m1A Human chr6 + 27503752 27503751 27503753 CAAAACTCGCTGACGCAGAGTTCTTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG CAAAACTCGCTGACGCAGAGTTCTTCCTCGTT__TATAGTGGTGAGTATCCCCGCCTGTCACGCG TAG T tRNA-Asp-GTC-2-1,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00005EA0AD tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1322959140 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_659727,Human_RBP_ID_1669385,Human_RBP_ID_5450952,Human_RBP_ID_18202604,Human_RBP_ID_23138308,Human_RBP_ID_24154220 68761 RMVar_ID_68761 Human_SNP_ID_270990777 m1A Human chr6 + 27503752 27503752 27503752 CAAAACTCGCTGACGCAGAGTTCTTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG CAAAACTCGCTGACGCAGAGTTCTTCCTCGTTGGTATAGTGGTGAGTATCCCCGCCTGTCACGCG A G tRNA-Asp-GTC-2-1,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00005EA0AD tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs545227769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659727,Human_RBP_ID_1669385,Human_RBP_ID_5450952,Human_RBP_ID_18202604,Human_RBP_ID_23138308,Human_RBP_ID_24154220 68762 RMVar_ID_68762 Human_SNP_ID_270990842 m1A Human chr6 + 27503800 27503800 27503800 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGAAAAGTTGCTTTTTGCA TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGCTTCCCCGACGGGGAGAAAAGTTGCTTTTTGCA A C tRNA-Asp-GTC-2-1,AB330774-001,AB330774-001:2,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00000711F0,RNACentral:URS00002B094D,RNACentral:URS00005EA0AD tRNA,misc_RNA,misc_RNA,tRNA intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1205178903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216794,Human_RBP_ID_1669386,Human_RBP_ID_8640534,Human_RBP_ID_17710254,Human_RBP_ID_18071909,Human_RBP_ID_18861164,Human_RBP_ID_22405152,Human_RBP_ID_22830639,Human_RBP_ID_23138309,Human_RBP_ID_24154221 68763 RMVar_ID_68763 Human_SNP_ID_270991382 m1A Human chr6 + 27505799 27505799 27505799 AGTTGCCTTTGGGGTGCAATTAGAAGGAAACTATTTGGGAGAAGTCAGGCTAAAACCAAACCGTA AGTTGCCTTTGGGGTGCAATTAGAAGGAAACTGTTTGGGAGAAGTCAGGCTAAAACCAAACCGTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:27505652..27505821 26863196 MeRIP-seq:(Medium) rs1561853708 Functional Loss SNV dbSNP153 33..33 33 - - - 68764 RMVar_ID_68764 Human_SNP_ID_270994511 m1A Human chr6 + 27519585 27519585 27519585 CTCTGGACTCTGAATCCAGCGATCCGAGTTCAAATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT CTCTGGACTCTGAATCCAGCGATCCGAGTTCACATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1009878003 Functional Loss SNV dbSNP153 33..33 33 - - - 68765 RMVar_ID_68765 Human_SNP_ID_270994512 m1A Human chr6 + 27519585 27519585 27519585 CTCTGGACTCTGAATCCAGCGATCCGAGTTCAAATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT CTCTGGACTCTGAATCCAGCGATCCGAGTTCAGATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1009878003 Functional Loss SNV dbSNP153 33..33 33 - - - 68766 RMVar_ID_68766 Human_SNP_ID_270994513 m1A Human chr6 + 27519585 27519585 27519585 CTCTGGACTCTGAATCCAGCGATCCGAGTTCAAATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT CTCTGGACTCTGAATCCAGCGATCCGAGTTCATATCTCGGTGGAACCTGTCGTTTCTTCTTGCTT A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1009878003 Functional Loss SNV dbSNP153 33..33 33 - - - 68767 RMVar_ID_68767 Human_SNP_ID_271001155 m1A Human chr6 + 27545755 27545755 27545755 GAAATCCATTGGGGTTTCCCCGCGCAGGTTCGAATCCTGCCGACTACGGTTTTACCAGGTGCAGT GAAATCCATTGGGGTTTCCCCGCGCAGGTTCGCATCCTGCCGACTACGGTTTTACCAGGTGCAGT A C TRS-TGA2-1,tRNA-Ser-TGA-2-1 RNACentral:URS000033EC0B,RNACentral:URS000037D0FB tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs979762966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8640550,Human_RBP_ID_18202609,Human_RBP_ID_18545652,Human_RBP_ID_18861192,Human_RBP_ID_21902279,Human_RBP_ID_22746423,Human_RBP_ID_22830655,Human_RBP_ID_23138355,Human_RBP_ID_24154248,Human_RBP_ID_26751461,Human_RBP_ID_26771722,Human_RBP_ID_27094197,Human_RBP_ID_27842388 68768 RMVar_ID_68768 Human_SNP_ID_271001169 m1A Human chr6 + 27545765 27545765 27545765 GGGGTTTCCCCGCGCAGGTTCGAATCCTGCCGACTACGGTTTTACCAGGTGCAGTTCCCGCCTTT GGGGTTTCCCCGCGCAGGTTCGAATCCTGCCGCCTACGGTTTTACCAGGTGCAGTTCCCGCCTTT A C TRS-TGA2-1,tRNA-Ser-TGA-2-1 RNACentral:URS000033EC0B,RNACentral:URS000037D0FB tRNA,tRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:27545749..27545851 26863410 MeRIP-seq:(Medium) rs146661525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216799,Human_RBP_ID_18211134,Human_RBP_ID_18545653,Human_RBP_ID_18861193,Human_RBP_ID_21902279,Human_RBP_ID_22746423,Human_RBP_ID_23138355,Human_RBP_ID_24154248,Human_RBP_ID_26771722,Human_RBP_ID_27842388 68769 RMVar_ID_68769 Human_SNP_ID_271001170 m1A Human chr6 + 27545765 27545765 27545765 GGGGTTTCCCCGCGCAGGTTCGAATCCTGCCGACTACGGTTTTACCAGGTGCAGTTCCCGCCTTT GGGGTTTCCCCGCGCAGGTTCGAATCCTGCCGGCTACGGTTTTACCAGGTGCAGTTCCCGCCTTT A G TRS-TGA2-1,tRNA-Ser-TGA-2-1 RNACentral:URS000033EC0B,RNACentral:URS000037D0FB tRNA,tRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:27545749..27545851 26863410 MeRIP-seq:(Medium) rs146661525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216799,Human_RBP_ID_18211134,Human_RBP_ID_18545653,Human_RBP_ID_18861193,Human_RBP_ID_21902279,Human_RBP_ID_22746423,Human_RBP_ID_23138355,Human_RBP_ID_24154248,Human_RBP_ID_26771722,Human_RBP_ID_27842388 68770 RMVar_ID_68770 Human_SNP_ID_271001199 m1A Human chr6 + 27545802 27545802 27545802 GGTTTTACCAGGTGCAGTTCCCGCCTTTCCTCAAAACTTACCCAAATTCTTGTACTCCATTTGCT GGTTTTACCAGGTGCAGTTCCCGCCTTTCCTCGAAACTTACCCAAATTCTTGTACTCCATTTGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:27545744..27545863 26863410 MeRIP-seq:(Medium) rs1279561103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1245616,Human_RBP_ID_9193006,Human_RBP_ID_18071922,Human_RBP_ID_21316654,Human_RBP_ID_22309640,Human_RBP_ID_26534728 68771 RMVar_ID_68771 Human_SNP_ID_271001797 m1A Human chr6 + 27547765 27547765 27547765 TATACATATATCTTCGAGCAGGTTCCACCGAGACTTGAACTCGGATCGCTGGATTCAGAGTCCAG TATACATATATCTTCGAGCAGGTTCCACCGAGCCTTGAACTCGGATCGCTGGATTCAGAGTCCAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27547686..27547844;chr6:27547675..27547807 26863196 MeRIP-seq:(Medium) rs72845016 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8231 68772 RMVar_ID_68772 Human_SNP_ID_271001798 m1A Human chr6 + 27547765 27547765 27547765 TATACATATATCTTCGAGCAGGTTCCACCGAGACTTGAACTCGGATCGCTGGATTCAGAGTCCAG TATACATATATCTTCGAGCAGGTTCCACCGAGTCTTGAACTCGGATCGCTGGATTCAGAGTCCAG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27547686..27547844;chr6:27547675..27547807 26863196 MeRIP-seq:(Medium) rs72845016 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8231 68773 RMVar_ID_68773 Human_SNP_ID_271011107 m1A Human chr6 - 27583464 27583464 27583464 TGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGACGAAGCAGTTGCTTTTGATTACAA TGTCACGCGGGAGACCGGGGTTCGATTCCCCGGCGGGGAGACGAAGCAGTTGCTTTTGATTACAA T C AB330774-001,tRNA-Asp-GTC-3-1,AB330774-001:2 RNACentral:URS00000711F0,RNACentral:URS00006D74B2,RNACentral:URS00002B094D misc_RNA,tRNA,misc_RNA exon,exon,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:27583391..27583504 26863196 MeRIP-seq:(Medium) rs1264667465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659746,Human_RBP_ID_1669414,Human_RBP_ID_2017103,Human_RBP_ID_5276707,Human_RBP_ID_5511190,Human_RBP_ID_8269925,Human_RBP_ID_8640564,Human_RBP_ID_9193012,Human_RBP_ID_18071934,Human_RBP_ID_18202617,Human_RBP_ID_18211183,Human_RBP_ID_18449999,Human_RBP_ID_18861212,Human_RBP_ID_23138385,Human_RBP_ID_23314951,Human_RBP_ID_24154264,Human_RBP_ID_27161303 68774 RMVar_ID_68774 Human_SNP_ID_271011122 m1A Human chr6 - 27583472 27583472 27583472 TCCCCGTCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGACGAAGCAGTTGCTTTT TCCCCGTCTGTCACGCGGGAGACCGGGGTTCGTTTCCCCGACGGGGAGACGAAGCAGTTGCTTTT T A AB330774-001,tRNA-Asp-GTC-3-1,AB330774-001:2 RNACentral:URS00000711F0,RNACentral:URS00006D74B2,RNACentral:URS00002B094D misc_RNA,tRNA,misc_RNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA untreated chr6:27583440..27583505 29072297,31548705,31548705,26863196 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs552698219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659746,Human_RBP_ID_1669414,Human_RBP_ID_2017103,Human_RBP_ID_8269925,Human_RBP_ID_8640564,Human_RBP_ID_9193012,Human_RBP_ID_10313126,Human_RBP_ID_18071934,Human_RBP_ID_18202617,Human_RBP_ID_18211183,Human_RBP_ID_18449999,Human_RBP_ID_22832685,Human_RBP_ID_23138385,Human_RBP_ID_24154264,Human_RBP_ID_26751525 68775 RMVar_ID_68775 Human_SNP_ID_271011123 m1A Human chr6 - 27583472 27583472 27583472 TCCCCGTCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGACGAAGCAGTTGCTTTT TCCCCGTCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGACGAAGCAGTTGCTTTT T C AB330774-001,tRNA-Asp-GTC-3-1,AB330774-001:2 RNACentral:URS00000711F0,RNACentral:URS00006D74B2,RNACentral:URS00002B094D misc_RNA,tRNA,misc_RNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA untreated chr6:27583440..27583505 29072297,31548705,31548705,26863196 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs552698219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659746,Human_RBP_ID_1669414,Human_RBP_ID_2017103,Human_RBP_ID_8269925,Human_RBP_ID_8640564,Human_RBP_ID_9193012,Human_RBP_ID_10313126,Human_RBP_ID_18071934,Human_RBP_ID_18202617,Human_RBP_ID_18211183,Human_RBP_ID_18449999,Human_RBP_ID_22832685,Human_RBP_ID_23138385,Human_RBP_ID_24154264,Human_RBP_ID_26751525 68776 RMVar_ID_68776 Human_SNP_ID_271011127 m1A Human chr6 + 27583476 27583476 27583476 GCAACTGCTTCGTCTCCCCGTCGGGGAATCGAACCCCGGTCTCCCGCGTGACAGACGGGGACACT GCAACTGCTTCGTCTCCCCGTCGGGGAATCGACCCCCGGTCTCCCGCGTGACAGACGGGGACACT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:27583373..27583525 26863196 MeRIP-seq:(Medium) rs1260340535 Functional Loss SNV dbSNP153 33..33 33 - - - 68777 RMVar_ID_68777 Human_SNP_ID_271011142 m1A Human chr6 - 27583485 27583485 27583485 ATAGTGGTGAGTGTCCCCGTCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGACGA ATAGTGGTGAGTGTCCCCGTCTGTCACGCGGGGGACCGGGGTTCGATTCCCCGACGGGGAGACGA T C AB330774-001,tRNA-Asp-GTC-3-1,AB330774-001:2 RNACentral:URS00000711F0,RNACentral:URS00006D74B2,RNACentral:URS00002B094D misc_RNA,tRNA,misc_RNA exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27583385..27583511 26863196 MeRIP-seq:(Medium) rs928593836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270809,Human_RBP_ID_659746,Human_RBP_ID_1216809,Human_RBP_ID_1245617,Human_RBP_ID_1669414,Human_RBP_ID_2017103,Human_RBP_ID_3804722,Human_RBP_ID_4877238,Human_RBP_ID_8269925,Human_RBP_ID_8640565,Human_RBP_ID_9193012,Human_RBP_ID_10278380,Human_RBP_ID_15772437,Human_RBP_ID_17423121,Human_RBP_ID_17710264,Human_RBP_ID_18202617,Human_RBP_ID_18211183,Human_RBP_ID_18861213,Human_RBP_ID_21392941,Human_RBP_ID_22309648,Human_RBP_ID_22832686,Human_RBP_ID_23138385,Human_RBP_ID_24154264,Human_RBP_ID_26534734,Human_RBP_ID_26714349,Human_RBP_ID_26751525,Human_RBP_ID_27094211,Human_RBP_ID_27344397 68778 RMVar_ID_68778 Human_SNP_ID_271011143 m1A Human chr6 - 27583485 27583485 27583485 ATAGTGGTGAGTGTCCCCGTCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGACGA ATAGTGGTGAGTGTCCCCGTCTGTCACGCGGGCGACCGGGGTTCGATTCCCCGACGGGGAGACGA T G AB330774-001,tRNA-Asp-GTC-3-1,AB330774-001:2 RNACentral:URS00000711F0,RNACentral:URS00006D74B2,RNACentral:URS00002B094D misc_RNA,tRNA,misc_RNA exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27583385..27583511 26863196 MeRIP-seq:(Medium) rs928593836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270809,Human_RBP_ID_659746,Human_RBP_ID_1216809,Human_RBP_ID_1245617,Human_RBP_ID_1669414,Human_RBP_ID_2017103,Human_RBP_ID_3804722,Human_RBP_ID_4877238,Human_RBP_ID_8269925,Human_RBP_ID_8640565,Human_RBP_ID_9193012,Human_RBP_ID_10278380,Human_RBP_ID_15772437,Human_RBP_ID_17423121,Human_RBP_ID_17710264,Human_RBP_ID_18202617,Human_RBP_ID_18211183,Human_RBP_ID_18861213,Human_RBP_ID_21392941,Human_RBP_ID_22309648,Human_RBP_ID_22832686,Human_RBP_ID_23138385,Human_RBP_ID_24154264,Human_RBP_ID_26534734,Human_RBP_ID_26714349,Human_RBP_ID_26751525,Human_RBP_ID_27094211,Human_RBP_ID_27344397 68779 RMVar_ID_68779 Human_SNP_ID_271011154 m1A Human chr6 + 27583494 27583494 27583494 CGTCGGGGAATCGAACCCCGGTCTCCCGCGTGACAGACGGGGACACTCACCACTATACTAACGAG CGTCGGGGAATCGAACCCCGGTCTCCCGCGTGCCAGACGGGGACACTCACCACTATACTAACGAG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27583382..27583525 26863196 MeRIP-seq:(Medium) rs774568336 Functional Loss SNV dbSNP153 33..33 33 - - - 68780 RMVar_ID_68780 Human_SNP_ID_271011155 m1A Human chr6 + 27583494 27583494 27583494 CGTCGGGGAATCGAACCCCGGTCTCCCGCGTGACAGACGGGGACACTCACCACTATACTAACGAG CGTCGGGGAATCGAACCCCGGTCTCCCGCGTGTCAGACGGGGACACTCACCACTATACTAACGAG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27583382..27583525 26863196 MeRIP-seq:(Medium) rs774568336 Functional Loss SNV dbSNP153 33..33 33 - - - 68781 RMVar_ID_68781 Human_SNP_ID_271013342 m1A Human chr6 - 27591829 27591829 27591829 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCAGGCGAACTTCAGAAGTTTTAC ATCAGACTTTTAATCTGAGGGTCCAGGGTTCACGTCCCTGTTCAGGCGAACTTCAGAAGTTTTAC T G tRNA-Lys-TTT-4-1 RNACentral:URS000072A930 tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1415711574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669419,Human_RBP_ID_2017105,Human_RBP_ID_5104611,Human_RBP_ID_5276709,Human_RBP_ID_8269927,Human_RBP_ID_8640568,Human_RBP_ID_17092145,Human_RBP_ID_18861218,Human_RBP_ID_21950324,Human_RBP_ID_22830668,Human_RBP_ID_23138390 68782 RMVar_ID_68782 Human_SNP_ID_271013623 m1A Human chr6 - 27592629 27592629 27592629 GAAGCATAAGCGGAGAAATGAGTGAATCTGCAAATGGGAGGTCTGAAAAATAAGGCGGTAGAGGA GAAGCATAAGCGGAGAAATGAGTGAATCTGCACATGGGAGGTCTGAAAAATAAGGCGGTAGAGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27592517..27592688 26863196 MeRIP-seq:(Medium) rs1187758508 Functional Loss SNV dbSNP153 33..33 33 - - - 68783 RMVar_ID_68783 Human_SNP_ID_271013734 m1A Human chr6 - 27592836 27592836 27592836 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTAGGTGCCTGTTTTTTTCC GCTGGGCCCATAACCCAGAGGTCGATGGATCGGAACCATCCTCTGCTAGGTGCCTGTTTTTTTCC T C tRNA-iMet-CAT-1-1,TRX-CAT1-1 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC tRNA,tRNA intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs987125924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326563,Human_RBP_ID_1669423,Human_RBP_ID_2017110,Human_RBP_ID_5622202,Human_RBP_ID_8640571,Human_RBP_ID_10278386,Human_RBP_ID_18861222,Human_RBP_ID_21392945,Human_RBP_ID_22102493,Human_RBP_ID_22832690,Human_RBP_ID_23138398,Human_RBP_ID_24154270,Human_RBP_ID_27344404 68784 RMVar_ID_68784 Human_SNP_ID_271013735 m1A Human chr6 - 27592836 27592836 27592836 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTAGGTGCCTGTTTTTTTCC GCTGGGCCCATAACCCAGAGGTCGATGGATCGCAACCATCCTCTGCTAGGTGCCTGTTTTTTTCC T G tRNA-iMet-CAT-1-1,TRX-CAT1-1 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC tRNA,tRNA intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs987125924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326563,Human_RBP_ID_1669423,Human_RBP_ID_2017110,Human_RBP_ID_5622202,Human_RBP_ID_8640571,Human_RBP_ID_10278386,Human_RBP_ID_18861222,Human_RBP_ID_21392945,Human_RBP_ID_22102493,Human_RBP_ID_22832690,Human_RBP_ID_23138398,Human_RBP_ID_24154270,Human_RBP_ID_27344404 68785 RMVar_ID_68785 Human_SNP_ID_271017584 m1A Human chr6 - 27605653 27605653 27605653 TCTTCTGGTCTCCGTATGGAGGCGTGGGTTCGAATCCCACTTCTGACACAGCCTGATCTTTTGTT TCTTCTGGTCTCCGTATGGAGGCGTGGGTTCGGATCCCACTTCTGACACAGCCTGATCTTTTGTT T C TRL-CAA2-1,TRL-CAA1-1-001,tRNA-Leu,tRNA-Leu-CAA-2-1,TRL-CAA1-2,tRNA-Leu:2 RNACentral:URS000067CB9E,RNACentral:URS0000224A3A,RNACentral:URS0000549EAC,RNACentral:URS0000572B72,RNACentral:URS000047F3CB,RNACentral:URS000044259A tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,intron,exon,exon,intron,exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1053037865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659755,Human_RBP_ID_1216818,Human_RBP_ID_1394798,Human_RBP_ID_1669430,Human_RBP_ID_3804729,Human_RBP_ID_4910381,Human_RBP_ID_5268393,Human_RBP_ID_5276712,Human_RBP_ID_5477874,Human_RBP_ID_5511193,Human_RBP_ID_7587176,Human_RBP_ID_8269937,Human_RBP_ID_8640578,Human_RBP_ID_8899347,Human_RBP_ID_9193016,Human_RBP_ID_10313128,Human_RBP_ID_15772459,Human_RBP_ID_17092143,Human_RBP_ID_17423114,Human_RBP_ID_17535271,Human_RBP_ID_18519216,Human_RBP_ID_18861229,Human_RBP_ID_21316690,Human_RBP_ID_22102495,Human_RBP_ID_22309657,Human_RBP_ID_22832692,Human_RBP_ID_23059205,Human_RBP_ID_23138404,Human_RBP_ID_23194973,Human_RBP_ID_24154277,Human_RBP_ID_24435499,Human_RBP_ID_24511980,Human_RBP_ID_25993044,Human_RBP_ID_27094222,Human_RBP_ID_27160991,Human_RBP_ID_27344407 68786 RMVar_ID_68786 Human_SNP_ID_271024013 m1A Human chr6 + 27631499 27631499 27631499 TATGTGCGGGTGATGCCGAGGTTGTGAGTTCGAGCCTCACCTGGAGCATGTTTTCTTCCAATTGC TATGTGCGGGTGATGCCGAGGTTGTGAGTTCGTGCCTCACCTGGAGCATGTTTTCTTCCAATTGC A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1332316871 Functional Loss SNV dbSNP153 33..33 33 - - - 68787 RMVar_ID_68787 Human_SNP_ID_271028502 m1A Human chr6 - 27650920 27650920 27650920 CCTGGATCAAAACCAGGCGGAAACAAGTGGTTACCCTTCTTACGTCTTGTTCCTGATCCTGAGAG CCTGGATCAAAACCAGGCGGAAACAAGTGGTTTCCCTTCTTACGTCTTGTTCCTGATCCTGAGAG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27650873..27651002 26863196 MeRIP-seq:(Medium) rs892173684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_5276715,Human_RBP_ID_5428283,Human_RBP_ID_5477875,Human_RBP_ID_5511195,Human_RBP_ID_8640588,Human_RBP_ID_10278391,Human_RBP_ID_15772489,Human_RBP_ID_18071952,Human_RBP_ID_18861244,Human_RBP_ID_21316704,Human_RBP_ID_22309667,Human_RBP_ID_22830685,Human_RBP_ID_23068733,Human_RBP_ID_23138417,Human_RBP_ID_23194977,Human_RBP_ID_24435504,Human_RBP_ID_24511987,Human_RBP_ID_25993055,Human_RBP_ID_27094229,Human_RBP_ID_27344418 68788 RMVar_ID_68788 Human_SNP_ID_271028503 m1A Human chr6 - 27650920 27650920 27650920 CCTGGATCAAAACCAGGCGGAAACAAGTGGTTACCCTTCTTACGTCTTGTTCCTGATCCTGAGAG CCTGGATCAAAACCAGGCGGAAACAAGTGGTTGCCCTTCTTACGTCTTGTTCCTGATCCTGAGAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27650873..27651002 26863196 MeRIP-seq:(Medium) rs892173684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_5276715,Human_RBP_ID_5428283,Human_RBP_ID_5477875,Human_RBP_ID_5511195,Human_RBP_ID_8640588,Human_RBP_ID_10278391,Human_RBP_ID_15772489,Human_RBP_ID_18071952,Human_RBP_ID_18861244,Human_RBP_ID_21316704,Human_RBP_ID_22309667,Human_RBP_ID_22830685,Human_RBP_ID_23068733,Human_RBP_ID_23138417,Human_RBP_ID_23194977,Human_RBP_ID_24435504,Human_RBP_ID_24511987,Human_RBP_ID_25993055,Human_RBP_ID_27094229,Human_RBP_ID_27344418 68789 RMVar_ID_68789 Human_SNP_ID_271028529 m1A Human chr6 - 27650943 27650943 27650943 GTTCGCCTAACACGCGAAAGGTCCCTGGATCAAAACCAGGCGGAAACAAGTGGTTACCCTTCTTA GTTCGCCTAACACGCGAAAGGTCCCTGGATCAGAACCAGGCGGAAACAAGTGGTTACCCTTCTTA T C tRNA-Val-AAC-3-1 RNACentral:URS0000750232 tRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs951473832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270921,Human_RBP_ID_284911,Human_RBP_ID_659768,Human_RBP_ID_1216831,Human_RBP_ID_1245621,Human_RBP_ID_1394806,Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_3804737,Human_RBP_ID_4910386,Human_RBP_ID_5104610,Human_RBP_ID_5268409,Human_RBP_ID_5276717,Human_RBP_ID_5477875,Human_RBP_ID_5622199,Human_RBP_ID_8269948,Human_RBP_ID_8640588,Human_RBP_ID_8899356,Human_RBP_ID_9193020,Human_RBP_ID_9308104,Human_RBP_ID_10313129,Human_RBP_ID_15772492,Human_RBP_ID_17667950,Human_RBP_ID_18071952,Human_RBP_ID_18202771,Human_RBP_ID_18211359,Human_RBP_ID_18450004,Human_RBP_ID_18519219,Human_RBP_ID_18861244,Human_RBP_ID_21221526,Human_RBP_ID_22309668,Human_RBP_ID_22513829,Human_RBP_ID_22830685,Human_RBP_ID_23059210,Human_RBP_ID_23138417,Human_RBP_ID_23194978,Human_RBP_ID_24154291,Human_RBP_ID_26045710,Human_RBP_ID_26534746,Human_RBP_ID_26751626,Human_RBP_ID_27094229,Human_RBP_ID_27160995,Human_RBP_ID_27344420,Human_RBP_ID_27522286,Human_RBP_ID_27568260,Human_RBP_ID_27754274 68790 RMVar_ID_68790 Human_SNP_ID_271028530 m1A Human chr6 - 27650943 27650943 27650943 GTTCGCCTAACACGCGAAAGGTCCCTGGATCAAAACCAGGCGGAAACAAGTGGTTACCCTTCTTA GTTCGCCTAACACGCGAAAGGTCCCTGGATCACAACCAGGCGGAAACAAGTGGTTACCCTTCTTA T G tRNA-Val-AAC-3-1 RNACentral:URS0000750232 tRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs951473832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270921,Human_RBP_ID_284911,Human_RBP_ID_659768,Human_RBP_ID_1216831,Human_RBP_ID_1245621,Human_RBP_ID_1394806,Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_3804737,Human_RBP_ID_4910386,Human_RBP_ID_5104610,Human_RBP_ID_5268409,Human_RBP_ID_5276717,Human_RBP_ID_5477875,Human_RBP_ID_5622199,Human_RBP_ID_8269948,Human_RBP_ID_8640588,Human_RBP_ID_8899356,Human_RBP_ID_9193020,Human_RBP_ID_9308104,Human_RBP_ID_10313129,Human_RBP_ID_15772492,Human_RBP_ID_17667950,Human_RBP_ID_18071952,Human_RBP_ID_18202771,Human_RBP_ID_18211359,Human_RBP_ID_18450004,Human_RBP_ID_18519219,Human_RBP_ID_18861244,Human_RBP_ID_21221526,Human_RBP_ID_22309668,Human_RBP_ID_22513829,Human_RBP_ID_22830685,Human_RBP_ID_23059210,Human_RBP_ID_23138417,Human_RBP_ID_23194978,Human_RBP_ID_24154291,Human_RBP_ID_26045710,Human_RBP_ID_26534746,Human_RBP_ID_26751626,Human_RBP_ID_27094229,Human_RBP_ID_27160995,Human_RBP_ID_27344420,Human_RBP_ID_27522286,Human_RBP_ID_27568260,Human_RBP_ID_27754274 68791 RMVar_ID_68791 Human_SNP_ID_271028553 m1A Human chr6 - 27650958 27650958 27650958 TGTAGTGGTTATCACGTTCGCCTAACACGCGAAAGGTCCCTGGATCAAAACCAGGCGGAAACAAG TGTAGTGGTTATCACGTTCGCCTAACACGCGAGAGGTCCCTGGATCAAAACCAGGCGGAAACAAG T C tRNA-Val-AAC-3-1 RNACentral:URS0000750232 tRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27650910..27650980 26863196 MeRIP-seq:(Medium) rs373235379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270814,Human_RBP_ID_659768,Human_RBP_ID_1216831,Human_RBP_ID_1245621,Human_RBP_ID_1394806,Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_3804737,Human_RBP_ID_4910386,Human_RBP_ID_5104610,Human_RBP_ID_5268409,Human_RBP_ID_5276717,Human_RBP_ID_5477875,Human_RBP_ID_5622199,Human_RBP_ID_8269948,Human_RBP_ID_8640588,Human_RBP_ID_15772493,Human_RBP_ID_17667950,Human_RBP_ID_18071952,Human_RBP_ID_18202771,Human_RBP_ID_18210960,Human_RBP_ID_18519219,Human_RBP_ID_18861244,Human_RBP_ID_21221526,Human_RBP_ID_22309668,Human_RBP_ID_22830685,Human_RBP_ID_23059210,Human_RBP_ID_23138417,Human_RBP_ID_23194978,Human_RBP_ID_24154291,Human_RBP_ID_26534746,Human_RBP_ID_26751626,Human_RBP_ID_27094229,Human_RBP_ID_27344420,Human_RBP_ID_27522286,Human_RBP_ID_27754274 68792 RMVar_ID_68792 Human_SNP_ID_271028566 m1A Human chr6 - 27650967 27650967 27650967 TTTCCGTAGTGTAGTGGTTATCACGTTCGCCTAACACGCGAAAGGTCCCTGGATCAAAACCAGGC TTTCCGTAGTGTAGTGGTTATCACGTTCGCCTGACACGCGAAAGGTCCCTGGATCAAAACCAGGC T C tRNA-Val-AAC-3-1,piR-43993,piR-43997 RNACentral:URS0000750232,RNACentral:URS000019078D,RNACentral:URS0000583064 tRNA,piRNA,piRNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs982771249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270814,Human_RBP_ID_659768,Human_RBP_ID_1216831,Human_RBP_ID_1669442,Human_RBP_ID_2017124,Human_RBP_ID_3804737,Human_RBP_ID_5622199,Human_RBP_ID_8269950,Human_RBP_ID_8640588,Human_RBP_ID_15772493,Human_RBP_ID_18202488,Human_RBP_ID_18210960,Human_RBP_ID_18861244,Human_RBP_ID_21316704,Human_RBP_ID_22830686,Human_RBP_ID_23138417,Human_RBP_ID_24154295,Human_RBP_ID_26751358,Human_RBP_ID_27344420,Human_RBP_ID_27522287,Human_RBP_ID_27568261 68793 RMVar_ID_68793 Human_SNP_ID_271033226 m1A Human chr6 - 27668670 27668670 27668670 AAAGGCCTCCCTTCAGGTAAGTGAAGGGCCCCACTATGGCATCCAGTGGCCCGTACGGGGATCGA AAAGGCCTCCCTTCAGGTAAGTGAAGGGCCCCGCTATGGCATCCAGTGGCCCGTACGGGGATCGA T C lnc-HIST1H2BL-1 RNACentral:URS00009C145C lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27668649..27668783 26863196 MeRIP-seq:(Medium) rs1003218978 Functional Loss SNV dbSNP153 33..33 33 - - - 68794 RMVar_ID_68794 Human_SNP_ID_271033227 m1A Human chr6 - 27668670 27668670 27668670 AAAGGCCTCCCTTCAGGTAAGTGAAGGGCCCCACTATGGCATCCAGTGGCCCGTACGGGGATCGA AAAGGCCTCCCTTCAGGTAAGTGAAGGGCCCCCCTATGGCATCCAGTGGCCCGTACGGGGATCGA T G lnc-HIST1H2BL-1 RNACentral:URS00009C145C lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27668649..27668783 26863196 MeRIP-seq:(Medium) rs1003218978 Functional Loss SNV dbSNP153 33..33 33 - - - 68795 RMVar_ID_68795 Human_SNP_ID_271033789 m1A Human chr6 - 27670580 27670580 27670580 GTCTGACTACGGATCAGAAGATTCTAGGTTCGACTCCTGGCTGGCTCGCTTGTGCTCTCACTTTT GTCTGACTACGGATCAGAAGATTCTAGGTTCGGCTCCTGGCTGGCTCGCTTGTGCTCTCACTTTT T C tRNA-Arg-ACG-2-1,piR-42844 RNACentral:URS00002DDD59,RNACentral:URS0000388381 tRNA,piRNA exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs529507320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659779,Human_RBP_ID_1216837,Human_RBP_ID_1326575,Human_RBP_ID_1394810,Human_RBP_ID_1669451,Human_RBP_ID_2017130,Human_RBP_ID_3804740,Human_RBP_ID_4910391,Human_RBP_ID_5277052,Human_RBP_ID_5428284,Human_RBP_ID_7587211,Human_RBP_ID_8269958,Human_RBP_ID_8640596,Human_RBP_ID_9193021,Human_RBP_ID_15772509,Human_RBP_ID_17092142,Human_RBP_ID_18071956,Human_RBP_ID_18450007,Human_RBP_ID_18861258,Human_RBP_ID_19032728,Human_RBP_ID_21316713,Human_RBP_ID_21947114,Human_RBP_ID_22102505,Human_RBP_ID_22830693,Human_RBP_ID_23068735,Human_RBP_ID_23110771,Human_RBP_ID_23138434,Human_RBP_ID_23314600,Human_RBP_ID_24154301,Human_RBP_ID_24437434,Human_RBP_ID_27522290 68796 RMVar_ID_68796 Human_SNP_ID_271034384 m1A Human chr6 - 27672465 27672465 27672465 GAAATCCAATGGGGGTTCCCCGCGCAGGTTCAAATCCTGCTCACAGCGTCGCCATTTTCTGGTTA GAAATCCAATGGGGGTTCCCCGCGCAGGTTCAGATCCTGCTCACAGCGTCGCCATTTTCTGGTTA T C tRNA-Ser-CGA-3-1 RNACentral:URS0000530C88 tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs564218365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659781,Human_RBP_ID_1143194,Human_RBP_ID_1216839,Human_RBP_ID_1394811,Human_RBP_ID_1669453,Human_RBP_ID_2017134,Human_RBP_ID_3804744,Human_RBP_ID_4877258,Human_RBP_ID_5276725,Human_RBP_ID_5428285,Human_RBP_ID_5477876,Human_RBP_ID_5511200,Human_RBP_ID_5622198,Human_RBP_ID_7587214,Human_RBP_ID_8269960,Human_RBP_ID_8640601,Human_RBP_ID_8899360,Human_RBP_ID_10278401,Human_RBP_ID_17710281,Human_RBP_ID_18071957,Human_RBP_ID_18861264,Human_RBP_ID_21316719,Human_RBP_ID_22309676,Human_RBP_ID_22830695,Human_RBP_ID_23138443,Human_RBP_ID_23194981,Human_RBP_ID_24154308,Human_RBP_ID_24437432,Human_RBP_ID_24511990,Human_RBP_ID_26041049,Human_RBP_ID_26714357,Human_RBP_ID_27094239,Human_RBP_ID_27344431,Human_RBP_ID_27522291 68797 RMVar_ID_68797 Human_SNP_ID_271038640 m1A Human chr6 + 27688246 27688246 27688246 GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGATCCCCGTACTGGCCAAGTATTCTCTGTGGCTT GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGGTCCCCGTACTGGCCAAGTATTCTCTGTGGCTT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs895825645 Functional Loss SNV dbSNP153 33..33 33 - - - 68798 RMVar_ID_68798 Human_SNP_ID_271038641 m1A Human chr6 + 27688246 27688246 27688246 GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGATCCCCGTACTGGCCAAGTATTCTCTGTGGCTT GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGTTCCCCGTACTGGCCAAGTATTCTCTGTGGCTT A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs895825645 Functional Loss SNV dbSNP153 33..33 33 - - - 68799 RMVar_ID_68799 Human_SNP_ID_271060639 m1A Human chr6 - 27777940 27777940 27777940 AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTAGATCCATCGACCTCTGGGTTATGGGCCCAGCA AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTTGATCCATCGACCTCTGGGTTATGGGCCCAGCA T A - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs9468225 Functional Loss SNV dbSNP153 33..33 33 - - - 68800 RMVar_ID_68800 Human_SNP_ID_271060640 m1A Human chr6 - 27777940 27777940 27777940 AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTAGATCCATCGACCTCTGGGTTATGGGCCCAGCA AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTGGATCCATCGACCTCTGGGTTATGGGCCCAGCA T C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs9468225 Functional Loss SNV dbSNP153 33..33 33 - - - 68801 RMVar_ID_68801 Human_SNP_ID_271060641 m1A Human chr6 - 27777940 27777940 27777940 AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTAGATCCATCGACCTCTGGGTTATGGGCCCAGCA AAAAAGCACCCTTCTTTAGCAGAGGATGGTTTCGATCCATCGACCTCTGGGTTATGGGCCCAGCA T G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs9468225 Functional Loss SNV dbSNP153 33..33 33 - - - 68802 RMVar_ID_68802 Human_SNP_ID_271060642 m1A Human chr6 + 27777941 27777941 27777941 GCTGGGCCCATAACCCAGAGGTCGATGGATCTAAACCATCCTCTGCTAAAGAAGGGTGCTTTTTT GCTGGGCCCATAACCCAGAGGTCGATGGATCTCAACCATCCTCTGCTAAAGAAGGGTGCTTTTTT A C tRNA-iMet-CAT-2-1,RF00017-4544 RNACentral:URS0000121433,RNACentral:URS000093B8FA tRNA,SRP RNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs986763668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669490,Human_RBP_ID_3804777,Human_RBP_ID_4910423,Human_RBP_ID_5219009,Human_RBP_ID_5268954,Human_RBP_ID_5277066,Human_RBP_ID_8640640,Human_RBP_ID_10278465,Human_RBP_ID_17535276,Human_RBP_ID_18071998,Human_RBP_ID_18174233,Human_RBP_ID_18519733,Human_RBP_ID_18861315,Human_RBP_ID_21316839,Human_RBP_ID_22832710,Human_RBP_ID_23068739,Human_RBP_ID_23138492,Human_RBP_ID_24154385,Human_RBP_ID_27094274 68803 RMVar_ID_68803 Human_SNP_ID_271060643 m1A Human chr6 + 27777941 27777941 27777941 GCTGGGCCCATAACCCAGAGGTCGATGGATCTAAACCATCCTCTGCTAAAGAAGGGTGCTTTTTT GCTGGGCCCATAACCCAGAGGTCGATGGATCTTAACCATCCTCTGCTAAAGAAGGGTGCTTTTTT A T tRNA-iMet-CAT-2-1,RF00017-4544 RNACentral:URS0000121433,RNACentral:URS000093B8FA tRNA,SRP RNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs986763668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669490,Human_RBP_ID_3804777,Human_RBP_ID_4910423,Human_RBP_ID_5219009,Human_RBP_ID_5268954,Human_RBP_ID_5277066,Human_RBP_ID_8640640,Human_RBP_ID_10278465,Human_RBP_ID_17535276,Human_RBP_ID_18071998,Human_RBP_ID_18174233,Human_RBP_ID_18519733,Human_RBP_ID_18861315,Human_RBP_ID_21316839,Human_RBP_ID_22832710,Human_RBP_ID_23068739,Human_RBP_ID_23138492,Human_RBP_ID_24154385,Human_RBP_ID_27094274 68804 RMVar_ID_68804 Human_SNP_ID_271063803 m1A Human chr6 - 27791371 27791367 27791372 CTCTGGACTCTGAATCCAGCGATCCGAGTTCAAATCTCGGTGGGACCCAGTCTGCTGTTTCAAGT CTCTGGACTCTGAATCCAGCGATCCGAGTTC_____TCGGTGGGACCCAGTCTGCTGTTTCAAGT AGATTT A tRNA-Gln-CTG-6-1 RNACentral:URS000064F320 tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1442748648 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_659816,Human_RBP_ID_1216857,Human_RBP_ID_1669494,Human_RBP_ID_2017174,Human_RBP_ID_3001335,Human_RBP_ID_4877352,Human_RBP_ID_5450970,Human_RBP_ID_7587337,Human_RBP_ID_8269972,Human_RBP_ID_8640646,Human_RBP_ID_15772955,Human_RBP_ID_17423111,Human_RBP_ID_17535280,Human_RBP_ID_18072002,Human_RBP_ID_18861319,Human_RBP_ID_21316874,Human_RBP_ID_22309719,Human_RBP_ID_22830716,Human_RBP_ID_23110768,Human_RBP_ID_23138496,Human_RBP_ID_24154390,Human_RBP_ID_26534760 68805 RMVar_ID_68805 Human_SNP_ID_271063810 m1A Human chr6 - 27791371 27791371 27791371 CTCTGGACTCTGAATCCAGCGATCCGAGTTCAAATCTCGGTGGGACCCAGTCTGCTGTTTCAAGT CTCTGGACTCTGAATCCAGCGATCCGAGTTCACATCTCGGTGGGACCCAGTCTGCTGTTTCAAGT T G tRNA-Gln-CTG-6-1 RNACentral:URS000064F320 tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1279145745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659816,Human_RBP_ID_1216857,Human_RBP_ID_1669494,Human_RBP_ID_2017174,Human_RBP_ID_3001335,Human_RBP_ID_4877352,Human_RBP_ID_5450970,Human_RBP_ID_7587337,Human_RBP_ID_8269972,Human_RBP_ID_8640646,Human_RBP_ID_15772955,Human_RBP_ID_17423111,Human_RBP_ID_17535280,Human_RBP_ID_18072002,Human_RBP_ID_18861319,Human_RBP_ID_21316874,Human_RBP_ID_22309719,Human_RBP_ID_22830716,Human_RBP_ID_23110768,Human_RBP_ID_23138496,Human_RBP_ID_24154390,Human_RBP_ID_26534760 68806 RMVar_ID_68806 Human_SNP_ID_271067877 m1A Human chr6 - 27807869 27807869 27807869 CGAGCTGGCCAAGTCTGCTCCCGCCCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCCCAGA CGAGCTGGCCAAGTCTGCTCCCGCCCCGAAGAGGGGCTCCAAGAAGGCGGTGACCAAGGCCCAGA T C H2BC13 Ensembl:ENSG00000185130 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27807789..27807899 26863196 MeRIP-seq:(Medium) rs148711105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659822,Human_RBP_ID_3969577,Human_RBP_ID_4877364,Human_RBP_ID_5478667,Human_RBP_ID_8640663,Human_RBP_ID_9400120,Human_RBP_ID_22104754,Human_RBP_ID_22460511,Human_RBP_ID_26353132,Human_RBP_ID_26829221,Human_RBP_ID_27094284,Human_RBP_ID_27344471 68807 RMVar_ID_68807 Human_SNP_ID_271078195 m1A Human chr6 - 27838625 27838624 27838625 GGGAGTAACTGCCGGAAAATTGGAGGAAAAAAACAGGAAGACGGTAGCTCTGTCAACCTACCGCT GGGAGTAACTGCCGGAAAATTGGAGGAAAAAA_CAGGAAGACGGTAGCTCTGTCAACCTACCGCT GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27838576..27838745 26863196 MeRIP-seq:(Medium) rs770490807 Functional Loss DEL dbSNP153 33..33 33 - - - 68808 RMVar_ID_68808 Human_SNP_ID_271078197 m1A Human chr6 - 27838625 27838625 27838625 GGGAGTAACTGCCGGAAAATTGGAGGAAAAAAACAGGAAGACGGTAGCTCTGTCAACCTACCGCT GGGAGTAACTGCCGGAAAATTGGAGGAAAAAAGCAGGAAGACGGTAGCTCTGTCAACCTACCGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27838576..27838745 26863196 MeRIP-seq:(Medium) rs762657486 Functional Loss SNV dbSNP153 33..33 33 - - - 68809 RMVar_ID_68809 Human_SNP_ID_271078198 m1A Human chr6 - 27838627 27838627 27838627 CTGGGAGTAACTGCCGGAAAATTGGAGGAAAAAAACAGGAAGACGGTAGCTCTGTCAACCTACCG CTGGGAGTAACTGCCGGAAAATTGGAGGAAAAGAACAGGAAGACGGTAGCTCTGTCAACCTACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:27838576..27838853;chr6:27838576..27838742 26863196 MeRIP-seq:(Medium) rs1159228360 Functional Loss SNV dbSNP153 33..33 33 - - - 68810 RMVar_ID_68810 Human_SNP_ID_271092721 m1A Human chr6 - 27893130 27893130 27893130 AGGTCGTTTTACCATGTCTGGACGTGGCAAGCAGGGCGGCAAGGCTCGCGCCAAGGCCAAAACCC AGGTCGTTTTACCATGTCTGGACGTGGCAAGCTGGGCGGCAAGGCTCGCGCCAAGGCCAAAACCC T A H2AC17 Ensembl:ENSG00000278677 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27892946..27893135;chr6:27892950..27893175;chr6:27892945..27893175 26863196 MeRIP-seq:(Medium) rs764459789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172992,Human_RBP_ID_270824,Human_RBP_ID_659923,Human_RBP_ID_1679077,Human_RBP_ID_4903756,Human_RBP_ID_5327084,Human_RBP_ID_5478671,Human_RBP_ID_5511233,Human_RBP_ID_9336021,Human_RBP_ID_15773537,Human_RBP_ID_22618069,Human_RBP_ID_23214708,Human_RBP_ID_24154517,Human_RBP_ID_26828092,Human_RBP_ID_27094382 68811 RMVar_ID_68811 Human_SNP_ID_271092899 m1A Human chr6 - 27893486 27893486 27893486 ACGGCTTTCTTGGAGCCCTTTTTGGGGGCAGGAGCAGATTTAGCCGGGTCGGGCATGGCGGAGGA ACGGCTTTCTTGGAGCCCTTTTTGGGGGCAGGCGCAGATTTAGCCGGGTCGGGCATGGCGGAGGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:27893426..27893599 26863196 MeRIP-seq:(Medium) rs145423069 Functional Loss SNV dbSNP153 33..33 33 - - - 68812 RMVar_ID_68812 Human_SNP_ID_271092935 m1A Human chr6 + 27893524 27893524 27893524 CCCCAAAAAGGGCTCCAAGAAAGCCGTAACCAAGGCCCAGAAAAAGGACGGCAAGAAGCGCAAGC CCCCAAAAAGGGCTCCAAGAAAGCCGTAACCACGGCCCAGAAAAAGGACGGCAAGAAGCGCAAGC A C H2BC17 Ensembl:ENSG00000274641 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27893475..27893637 26863196 MeRIP-seq:(Medium) rs1184234918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4877544,Human_RBP_ID_9400143,Human_RBP_ID_22462538,Human_RBP_ID_22706173,Human_RBP_ID_27094384,Human_RBP_ID_27344553 68813 RMVar_ID_68813 Human_SNP_ID_271092944 m1A Human chr6 + 27893530 27893530 27893530 AAAGGGCTCCAAGAAAGCCGTAACCAAGGCCCAGAAAAAGGACGGCAAGAAGCGCAAGCGCAGCC AAAGGGCTCCAAGAAAGCCGTAACCAAGGCCCGGAAAAAGGACGGCAAGAAGCGCAAGCGCAGCC A G H2BC17 Ensembl:ENSG00000274641 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:27893481..27893599 26863196 MeRIP-seq:(Medium) rs1561948990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3001458,Human_RBP_ID_4877544,Human_RBP_ID_9400143,Human_RBP_ID_22706173,Human_RBP_ID_27094384,Human_RBP_ID_27344553 68814 RMVar_ID_68814 Human_SNP_ID_271092973 m1A Human chr6 - 27893577 27893574 27893578 GACTTGCTTCAGCACCTTGTACACGTAGATAGAGTAACTCTCTTTGCGGCTGCGCTTGCGCTTCT GACTTGCTTCAGCACCTTGTACACGTAGATA____AACTCTCTTTGCGGCTGCGCTTGCGCTTCT TACTC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27893426..27893600 26863196 MeRIP-seq:(Medium) rs1452823838 Functional Loss DEL dbSNP153 32..35 33 - - - 68815 RMVar_ID_68815 Human_SNP_ID_271095385 m1A Human chr6 - 27902923 27902923 27902923 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCAATGCAACGATGACGTTTTATTC TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGGTTCCCGGCCAATGCAACGATGACGTTTTATTC T C piR-33487,piR-33486,tRNA-Gly-GCC-2-1,piR-36173,TRG2 RNACentral:URS000044CE8A,RNACentral:URS000044DA37,RNACentral:URS000013B42D,RNACentral:URS000043000B,RNACentral:URS00005AFD62 piRNA,piRNA,tRNA,piRNA,tRNA intron,intron,intron,intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs560509571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659942,Human_RBP_ID_1669636,Human_RBP_ID_5268429,Human_RBP_ID_5276739,Human_RBP_ID_7587597,Human_RBP_ID_8640781,Human_RBP_ID_15773769,Human_RBP_ID_17710307,Human_RBP_ID_18174234,Human_RBP_ID_18861397,Human_RBP_ID_21317101,Human_RBP_ID_22309838,Human_RBP_ID_22830775,Human_RBP_ID_23138519,Human_RBP_ID_27161019,Human_RBP_ID_27522386 68816 RMVar_ID_68816 Human_SNP_ID_271140612 m1A Human chr6 + 28123169 28123169 28123169 AGTTTCAGGCTGCAGTAAGCTATGATCGCACCACTCACTGCACTCCAGTCTGGGTGACAGAGTGA AGTTTCAGGCTGCAGTAAGCTATGATCGCACCGCTCACTGCACTCCAGTCTGGGTGACAGAGTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:28123118..28125680 26863196 MeRIP-seq:(Medium) rs1197767640 Functional Loss SNV dbSNP153 33..33 33 - - - 68817 RMVar_ID_68817 Human_SNP_ID_271140621 m1A Human chr6 - 28123191 28123191 28123191 CCTTTGTTTTAGGAGATGGGTCTCACTCTGTCACCCAGACTGGAGTGCAGTGAGTGGTGCGATCA CCTTTGTTTTAGGAGATGGGTCTCACTCTGTCGCCCAGACTGGAGTGCAGTGAGTGGTGCGATCA T C ZSCAN16-AS1 Ensembl:ENSG00000269293 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:28123140..28123248 26863196 MeRIP-seq:(Medium) rs772861884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_659970,Human_RBP_ID_950598,Human_RBP_ID_4877589,Human_RBP_ID_5218735,Human_RBP_ID_8217009 Human_Splice_Rec_746254,Human_Splice_Rec_746258,Human_Splice_Rec_746260 68818 RMVar_ID_68818 Human_SNP_ID_271144555 m1A Human chr6 + 28141944 28141944 28141944 GGCCGGAGGGGCCTGGTCCGAGTACAGCTTTCATCGCCTTTACTCCCCGACCTTCCTTCGAGTCT GGCCGGAGGGGCCTGGTCCGAGTACAGCTTTCGTCGCCTTTACTCCCCGACCTTCCTTCGAGTCT A G ZKSCAN8 Ensembl:ENSG00000198315 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28141893..28141986 26863196 MeRIP-seq:(Medium) rs1323801429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903762,Human_RBP_ID_5152572,Human_RBP_ID_18425377,Human_RBP_ID_22309866,Human_RBP_ID_23059272 Human_Splice_Rec_746277,Human_Splice_Rec_746287,Human_Splice_Rec_746297 68819 RMVar_ID_68819 Human_SNP_ID_271144556 m1A Human chr6 + 28141944 28141944 28141944 GGCCGGAGGGGCCTGGTCCGAGTACAGCTTTCATCGCCTTTACTCCCCGACCTTCCTTCGAGTCT GGCCGGAGGGGCCTGGTCCGAGTACAGCTTTCTTCGCCTTTACTCCCCGACCTTCCTTCGAGTCT A T ZKSCAN8 Ensembl:ENSG00000198315 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28141893..28141986 26863196 MeRIP-seq:(Medium) rs1323801429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903762,Human_RBP_ID_5152572,Human_RBP_ID_18425377,Human_RBP_ID_22309866,Human_RBP_ID_23059272 Human_Splice_Rec_746277,Human_Splice_Rec_746287,Human_Splice_Rec_746297 68820 RMVar_ID_68820 Human_SNP_ID_271162297 m1A Human chr6 + 28225463 28225463 28225463 TGGAAAGTGAACCTCAGCCGCTGGGAAGTGGGAGCCGGAGGAGGGGGCGGCGGTCAGTGCCGGGC TGGAAAGTGAACCTCAGCCGCTGGGAAGTGGGCGCCGGAGGAGGGGGCGGCGGTCAGTGCCGGGC A C ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:28225315..28225629 26863196 MeRIP-seq:(Medium) rs1247631598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951178,Human_RBP_ID_5327362,Human_RBP_ID_9437754,Human_RBP_ID_26353523,Human_RBP_ID_27842389 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696 68821 RMVar_ID_68821 Human_SNP_ID_271163537 m1A Human chr6 + 28230751 28230751 28230751 AATGATACAGTGTGTTAAAAGGTGATGAGGCTATGGAATAAGGCAAAAATAGAACAGGATAAGGG AATGATACAGTGTGTTAAAAGGTGATGAGGCTGTGGAATAAGGCAAAAATAGAACAGGATAAGGG A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:28230700..28230899 26863196 MeRIP-seq:(Medium) rs1014811060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15775867 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794 68822 RMVar_ID_68822 Human_SNP_ID_271171616 m1A Human chr6 + 28267634 28267634 28267634 AGGAATAACGGGGAGACCAGAGCGGTTGGAGCAGTGAACAAAGGCGACCTTTGTAGGGAATGATG AGGAATAACGGGGAGACCAGAGCGGTTGGAGCGGTGAACAAAGGCGACCTTTGTAGGGAATGATG A G ZSCAN26,AL021997.3 Ensembl:ENSG00000197062,Ensembl:ENSG00000276302 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:28267592..28267704 26863196 MeRIP-seq:(Medium) rs993336745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15776175 68823 RMVar_ID_68823 Human_SNP_ID_271172671 m1A Human chr6 + 28272778 28272777 28272779 TTCGGCATGAGTGTGAAGTTACAAAGCCTGAGAAAGAGAAGGGTAAGAATTGGATTGCATCTTCT TTCGGCATGAGTGTGAAGTTACAAAGCCTGAG__AGAGAAGGGTAAGAATTGGATTGCATCTTCT GAA G ZSCAN26,AL021997.3 Ensembl:ENSG00000197062,Ensembl:ENSG00000276302 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:28272727..28281348 32194978 MeRIP-seq:(Medium) rs759979753 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2017320,Human_RBP_ID_15776262,Human_RBP_ID_26353525 Human_Splice_Rec_746403,Human_Splice_Rec_746409,Human_Splice_Rec_746421,Human_Splice_Rec_746427,Human_Splice_Rec_746433,Human_Splice_Rec_746439 RMVar_hsa_circ_121281,RMVar_hsa_circ_296930,RMVar_hsa_circ_10422,RMVar_hsa_circ_237797 68824 RMVar_ID_68824 Human_SNP_ID_271188751 m1A Human chr6 + 28350015 28350015 28350015 GGCGTCGGCCTTCCACTGTGGGGTTAAATCTCATCCCGCGGCTCTCCTCCTGTCGGTCCTGCAGT GGCGTCGGCCTTCCACTGTGGGGTTAAATCTCCTCCCGCGGCTCTCCTCCTGTCGGTCCTGCAGT A C ZKSCAN3 Ensembl:ENSG00000189298 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28349964..28350150 26863196 MeRIP-seq:(Medium) rs1163300876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4877859,Human_RBP_ID_24155067 Human_Splice_Rec_746563,Human_Splice_Rec_746573,Human_Splice_Rec_746581 68825 RMVar_ID_68825 Human_SNP_ID_271188838 m1A Human chr6 + 28350321 28350321 28350321 CGGGTCGGTTCTTGAGGGTATTTGGAGACGGGATGCATGGGTCACATAGACAAGCCTCGAGAATG CGGGTCGGTTCTTGAGGGTATTTGGAGACGGGGTGCATGGGTCACATAGACAAGCCTCGAGAATG A G ZKSCAN3 Ensembl:ENSG00000189298 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:28350252..28350342 26863196 MeRIP-seq:(Medium) rs1243168120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5656255 Human_Splice_Rec_746582,Human_Splice_Rec_746583 68826 RMVar_ID_68826 Human_SNP_ID_271195757 m1A Human chr6 + 28383349 28383349 28383349 GCCCAACCTCACCAGAGACACTGAAAGGCCGGAGCGCACGAATCTGAAACCACCCGCCTCCAAAG GCCCAACCTCACCAGAGACACTGAAAGGCCGGTGCGCACGAATCTGAAACCACCCGCCTCCAAAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:28383262..28383369 26863196 MeRIP-seq:(Medium) rs1392947029 Functional Loss SNV dbSNP153 33..33 33 - - - 68827 RMVar_ID_68827 Human_SNP_ID_271199208 m1A Human chr6 - 28399684 28399684 28399684 TCGAGGCCTCTTGCCTTCGCTCCGTAGGAGGGAGTTCTCTTCTGGCCCTGGGGGCCGCAGGTGAG TCGAGGCCTCTTGCCTTCGCTCCGTAGGAGGGCGTTCTCTTCTGGCCCTGGGGGCCGCAGGTGAG T G ZSCAN12 Ensembl:ENSG00000158691 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28399621..28399686 26863196 MeRIP-seq:(Medium) rs1045178897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903774,Human_RBP_ID_18425378 Human_Splice_Rec_746593,Human_Splice_Rec_746601 68828 RMVar_ID_68828 Human_SNP_ID_271242581 m1A Human chr6 - 28597355 28597355 28597355 CTAATCCATTGTGCTCTGCACGCGTGGGTTCGAATCCCATCCTCGTCGTTTCTGGAGGTTTTTAT CTAATCCATTGTGCTCTGCACGCGTGGGTTCGTATCCCATCCTCGTCGTTTCTGGAGGTTTTTAT T A ZBED9 Ensembl:ENSG00000232040 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1437574055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82065,Human_RBP_ID_168896,Human_RBP_ID_1669837,Human_RBP_ID_5277088,Human_RBP_ID_8641018,Human_RBP_ID_10278926,Human_RBP_ID_15777884,Human_RBP_ID_17423214,Human_RBP_ID_18545658,Human_RBP_ID_18861709,Human_RBP_ID_21318908,Human_RBP_ID_22832737,Human_RBP_ID_23138574,Human_RBP_ID_24513740,Human_RBP_ID_24554789,Human_RBP_ID_26764641,Human_RBP_ID_27161024,Human_RBP_ID_27522519 68829 RMVar_ID_68829 Human_SNP_ID_271257950 m1A Human chr6 - 28658252 28658252 28658252 GCATGCTTAGCATGCATGAGGTCCCGGGTTCGATCCCCAGCATCTCCAGTGTTTTTGTATTTATG GCATGCTTAGCATGCATGAGGTCCCGGGTTCGTTCCCCAGCATCTCCAGTGTTTTTGTATTTATG T A tRNA-Ala-AGC-4-1 RNACentral:URS0000209048 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs575832318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12929,Human_RBP_ID_284932,Human_RBP_ID_660255,Human_RBP_ID_1046450,Human_RBP_ID_1216930,Human_RBP_ID_1326665,Human_RBP_ID_1394888,Human_RBP_ID_1669856,Human_RBP_ID_2017505,Human_RBP_ID_3805264,Human_RBP_ID_4910660,Human_RBP_ID_5268453,Human_RBP_ID_5511271,Human_RBP_ID_5536145,Human_RBP_ID_5622221,Human_RBP_ID_7589124,Human_RBP_ID_8269997,Human_RBP_ID_8641037,Human_RBP_ID_8899486,Human_RBP_ID_9193185,Human_RBP_ID_9336023,Human_RBP_ID_15777915,Human_RBP_ID_17710349,Human_RBP_ID_18072581,Human_RBP_ID_18183987,Human_RBP_ID_18210975,Human_RBP_ID_18450029,Human_RBP_ID_18519234,Human_RBP_ID_18539990,Human_RBP_ID_18861730,Human_RBP_ID_21318958,Human_RBP_ID_22405176,Human_RBP_ID_22616027,Human_RBP_ID_22830831,Human_RBP_ID_23138601,Human_RBP_ID_23195000,Human_RBP_ID_24155345,Human_RBP_ID_24435546,Human_RBP_ID_24512057,Human_RBP_ID_24536462,Human_RBP_ID_26714521,Human_RBP_ID_26771726,Human_RBP_ID_27094709,Human_RBP_ID_27344751,Human_RBP_ID_27522530,Human_RBP_ID_27754602 68830 RMVar_ID_68830 Human_SNP_ID_271257951 m1A Human chr6 - 28658252 28658252 28658252 GCATGCTTAGCATGCATGAGGTCCCGGGTTCGATCCCCAGCATCTCCAGTGTTTTTGTATTTATG GCATGCTTAGCATGCATGAGGTCCCGGGTTCGGTCCCCAGCATCTCCAGTGTTTTTGTATTTATG T C tRNA-Ala-AGC-4-1 RNACentral:URS0000209048 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs575832318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12929,Human_RBP_ID_284932,Human_RBP_ID_660255,Human_RBP_ID_1046450,Human_RBP_ID_1216930,Human_RBP_ID_1326665,Human_RBP_ID_1394888,Human_RBP_ID_1669856,Human_RBP_ID_2017505,Human_RBP_ID_3805264,Human_RBP_ID_4910660,Human_RBP_ID_5268453,Human_RBP_ID_5511271,Human_RBP_ID_5536145,Human_RBP_ID_5622221,Human_RBP_ID_7589124,Human_RBP_ID_8269997,Human_RBP_ID_8641037,Human_RBP_ID_8899486,Human_RBP_ID_9193185,Human_RBP_ID_9336023,Human_RBP_ID_15777915,Human_RBP_ID_17710349,Human_RBP_ID_18072581,Human_RBP_ID_18183987,Human_RBP_ID_18210975,Human_RBP_ID_18450029,Human_RBP_ID_18519234,Human_RBP_ID_18539990,Human_RBP_ID_18861730,Human_RBP_ID_21318958,Human_RBP_ID_22405176,Human_RBP_ID_22616027,Human_RBP_ID_22830831,Human_RBP_ID_23138601,Human_RBP_ID_23195000,Human_RBP_ID_24155345,Human_RBP_ID_24435546,Human_RBP_ID_24512057,Human_RBP_ID_24536462,Human_RBP_ID_26714521,Human_RBP_ID_26771726,Human_RBP_ID_27094709,Human_RBP_ID_27344751,Human_RBP_ID_27522530,Human_RBP_ID_27754602 68831 RMVar_ID_68831 Human_SNP_ID_271257981 m1A Human chr6 - 28658273 28658273 28658273 GATGTAGCTCAGTGGTAGAGCGCATGCTTAGCATGCATGAGGTCCCGGGTTCGATCCCCAGCATC GATGTAGCTCAGTGGTAGAGCGCATGCTTAGCTTGCATGAGGTCCCGGGTTCGATCCCCAGCATC T A tRNA-Ala-AGC-4-1 RNACentral:URS0000209048 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1054895254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660255,Human_RBP_ID_1046451,Human_RBP_ID_1216930,Human_RBP_ID_1326666,Human_RBP_ID_1394888,Human_RBP_ID_1669856,Human_RBP_ID_2017505,Human_RBP_ID_3001960,Human_RBP_ID_3805264,Human_RBP_ID_4910662,Human_RBP_ID_5268455,Human_RBP_ID_5536145,Human_RBP_ID_5622221,Human_RBP_ID_7589124,Human_RBP_ID_8269997,Human_RBP_ID_8641037,Human_RBP_ID_8899486,Human_RBP_ID_10278936,Human_RBP_ID_15777916,Human_RBP_ID_17041961,Human_RBP_ID_17710350,Human_RBP_ID_18072582,Human_RBP_ID_18450029,Human_RBP_ID_18519234,Human_RBP_ID_18539990,Human_RBP_ID_18861730,Human_RBP_ID_21318958,Human_RBP_ID_22102648,Human_RBP_ID_22310128,Human_RBP_ID_22830832,Human_RBP_ID_23068754,Human_RBP_ID_23138601,Human_RBP_ID_23195001,Human_RBP_ID_24155345,Human_RBP_ID_24435547,Human_RBP_ID_24513736,Human_RBP_ID_26041078,Human_RBP_ID_26534901,Human_RBP_ID_26764364,Human_RBP_ID_27094710,Human_RBP_ID_27161029,Human_RBP_ID_27344752,Human_RBP_ID_27522531,Human_RBP_ID_27568288,Human_RBP_ID_27754602 68832 RMVar_ID_68832 Human_SNP_ID_271257982 m1A Human chr6 - 28658273 28658273 28658273 GATGTAGCTCAGTGGTAGAGCGCATGCTTAGCATGCATGAGGTCCCGGGTTCGATCCCCAGCATC GATGTAGCTCAGTGGTAGAGCGCATGCTTAGCGTGCATGAGGTCCCGGGTTCGATCCCCAGCATC T C tRNA-Ala-AGC-4-1 RNACentral:URS0000209048 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1054895254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660255,Human_RBP_ID_1046451,Human_RBP_ID_1216930,Human_RBP_ID_1326666,Human_RBP_ID_1394888,Human_RBP_ID_1669856,Human_RBP_ID_2017505,Human_RBP_ID_3001960,Human_RBP_ID_3805264,Human_RBP_ID_4910662,Human_RBP_ID_5268455,Human_RBP_ID_5536145,Human_RBP_ID_5622221,Human_RBP_ID_7589124,Human_RBP_ID_8269997,Human_RBP_ID_8641037,Human_RBP_ID_8899486,Human_RBP_ID_10278936,Human_RBP_ID_15777916,Human_RBP_ID_17041961,Human_RBP_ID_17710350,Human_RBP_ID_18072582,Human_RBP_ID_18450029,Human_RBP_ID_18519234,Human_RBP_ID_18539990,Human_RBP_ID_18861730,Human_RBP_ID_21318958,Human_RBP_ID_22102648,Human_RBP_ID_22310128,Human_RBP_ID_22830832,Human_RBP_ID_23068754,Human_RBP_ID_23138601,Human_RBP_ID_23195001,Human_RBP_ID_24155345,Human_RBP_ID_24435547,Human_RBP_ID_24513736,Human_RBP_ID_26041078,Human_RBP_ID_26534901,Human_RBP_ID_26764364,Human_RBP_ID_27094710,Human_RBP_ID_27161029,Human_RBP_ID_27344752,Human_RBP_ID_27522531,Human_RBP_ID_27568288,Human_RBP_ID_27754602 68833 RMVar_ID_68833 Human_SNP_ID_271276064 m1A Human chr6 + 28729328 28729328 28729328 CAGAACTCTCATGCGGTCAGGGGGTGTAGCTCAGTGGTAGAGCGCGTGCTTCGCATGTACGAGGC CAGAACTCTCATGCGGTCAGGGGGTGTAGCTCGGTGGTAGAGCGCGTGCTTCGCATGTACGAGGC A G piR-36253,piR-36257,piR-36258,tRNA-Ala-CGC-4-1,piR-36255,piR-36272,piR-36254,piR-36252,piR-36685,piR-36270,piR-36256 RNACentral:URS000007B044,RNACentral:URS00005DADAC,RNACentral:URS00004570F0,RNACentral:URS000038D768,RNACentral:URS00001B460B,RNACentral:URS000054C938,RNACentral:URS000042B8BF,RNACentral:URS000036A083,RNACentral:URS0000037542,RNACentral:URS00003C63C6,RNACentral:URS000037F5E2 piRNA,piRNA,piRNA,tRNA,piRNA,piRNA,piRNA,piRNA,piRNA,piRNA,piRNA intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:28729320..28729447 26863196 MeRIP-seq:(Medium) rs1275328968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660264,Human_RBP_ID_1216946,Human_RBP_ID_1394902,Human_RBP_ID_1669888,Human_RBP_ID_2017525,Human_RBP_ID_3805277,Human_RBP_ID_4878044,Human_RBP_ID_5268467,Human_RBP_ID_5277105,Human_RBP_ID_5305673,Human_RBP_ID_7589156,Human_RBP_ID_8270012,Human_RBP_ID_8641068,Human_RBP_ID_8899499,Human_RBP_ID_15777969,Human_RBP_ID_17423186,Human_RBP_ID_17710356,Human_RBP_ID_18861766,Human_RBP_ID_22513882,Human_RBP_ID_22830848,Human_RBP_ID_23112052,Human_RBP_ID_23138643,Human_RBP_ID_24155360,Human_RBP_ID_26534904,Human_RBP_ID_27161318,Human_RBP_ID_27754607 68834 RMVar_ID_68834 Human_SNP_ID_271276119 m1A Human chr6 + 28729371 28729371 28729371 GCGTGCTTCGCATGTACGAGGCCCCGGGTTCGACCCCCGGCTCCTCCAGTTGTCCATTTTCTTCA GCGTGCTTCGCATGTACGAGGCCCCGGGTTCGCCCCCCGGCTCCTCCAGTTGTCCATTTTCTTCA A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:28729323..28729423;chr6:28729328..28729463;chr6:28729328..28729429;chr6:28729317..28729487 29072297,31548705,26863196 m1A-MAP&m1A-IP-seq:(High) rs1303150076 Functional Loss SNV dbSNP153 33..33 33 - - - 68835 RMVar_ID_68835 Human_SNP_ID_271276147 m1A Human chr6 - 28729388 28729388 28729388 AGAACCAGAAAGGAGAATGAAGAAAATGGACAACTGGAGGAGCCGGGGGTCGAACCCGGGGCCTC AGAACCAGAAAGGAGAATGAAGAAAATGGACAGCTGGAGGAGCCGGGGGTCGAACCCGGGGCCTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:28729323..28729422 26863410 MeRIP-seq:(Medium) rs144282806 Functional Loss SNV dbSNP153 33..33 33 - - - 68836 RMVar_ID_68836 Human_SNP_ID_271276148 m1A Human chr6 - 28729388 28729388 28729388 AGAACCAGAAAGGAGAATGAAGAAAATGGACAACTGGAGGAGCCGGGGGTCGAACCCGGGGCCTC AGAACCAGAAAGGAGAATGAAGAAAATGGACACCTGGAGGAGCCGGGGGTCGAACCCGGGGCCTC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:28729323..28729422 26863410 MeRIP-seq:(Medium) rs144282806 Functional Loss SNV dbSNP153 33..33 33 - - - 68837 RMVar_ID_68837 Human_SNP_ID_271277935 m1A Human chr6 - 28735444 28735444 28735444 GTATGCTTAACATTCATGAGGCTCTGGGTTCGATCCCCAGCACTTCCACAAGTACATTTCCTTAT GTATGCTTAACATTCATGAGGCTCTGGGTTCGGTCCCCAGCACTTCCACAAGTACATTTCCTTAT T C tRNA-Val-AAC-6-1,TRV-AAC6-1 RNACentral:URS000071ED2F,RNACentral:URS00006CFACA tRNA,tRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1169813404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216952,Human_RBP_ID_1326678,Human_RBP_ID_1394906,Human_RBP_ID_1669890,Human_RBP_ID_2017527,Human_RBP_ID_3029237,Human_RBP_ID_3805281,Human_RBP_ID_5268471,Human_RBP_ID_5276766,Human_RBP_ID_7589162,Human_RBP_ID_8270016,Human_RBP_ID_8641072,Human_RBP_ID_8899503,Human_RBP_ID_10278942,Human_RBP_ID_15777975,Human_RBP_ID_18072598,Human_RBP_ID_18861770,Human_RBP_ID_21319016,Human_RBP_ID_21950339,Human_RBP_ID_22102659,Human_RBP_ID_22310144,Human_RBP_ID_22830855,Human_RBP_ID_23059394,Human_RBP_ID_23138646,Human_RBP_ID_24155364,Human_RBP_ID_24512067,Human_RBP_ID_26041040,Human_RBP_ID_26714533,Human_RBP_ID_27094734,Human_RBP_ID_27754610 68838 RMVar_ID_68838 Human_SNP_ID_271281450 m1A Human chr6 + 28747800 28747800 28747800 CATCAGACTTTTAATCTGACGGTGCAGGGTTCAAGTCCCTGTTCAGGCGAAATATTTGTGTGTTT CATCAGACTTTTAATCTGACGGTGCAGGGTTCGAGTCCCTGTTCAGGCGAAATATTTGTGTGTTT A G tRNA-Lys-TTT-7-1,TRK-TTT7-1 RNACentral:URS00006CC2CC,RNACentral:URS00006DBB6C tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs948924982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1142392,Human_RBP_ID_1394914,Human_RBP_ID_1669897,Human_RBP_ID_2017535,Human_RBP_ID_3805289,Human_RBP_ID_7589174,Human_RBP_ID_8141178,Human_RBP_ID_8270020,Human_RBP_ID_8641083,Human_RBP_ID_8899506,Human_RBP_ID_15777985,Human_RBP_ID_17710361,Human_RBP_ID_18072602,Human_RBP_ID_18861782,Human_RBP_ID_21319028,Human_RBP_ID_21950328,Human_RBP_ID_22830864,Human_RBP_ID_23059396,Human_RBP_ID_23138658,Human_RBP_ID_24155368,Human_RBP_ID_24437411,Human_RBP_ID_27754612 68839 RMVar_ID_68839 Human_SNP_ID_271284448 m1A Human chr6 - 28758370 28758370 28758370 GCATGTGTGAGGCCCCGGGTTCGATCCCCGGCACCTCCAAATGGTGGTTTTGCTCTGGCAGTGCT GCATGTGTGAGGCCCCGGGTTCGATCCCCGGCTCCTCCAAATGGTGGTTTTGCTCTGGCAGTGCT T A tRNA-Ala-TGC-6-1,piR-49039 RNACentral:URS00006C133C,RNACentral:URS000000AA0C tRNA,piRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28758322..28758419 26863196 MeRIP-seq:(Medium) rs898537853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660267,Human_RBP_ID_1046456,Human_RBP_ID_1679108,Human_RBP_ID_2017538,Human_RBP_ID_3805292,Human_RBP_ID_4910681,Human_RBP_ID_5428328,Human_RBP_ID_5451007,Human_RBP_ID_7589183,Human_RBP_ID_8270023,Human_RBP_ID_8641089,Human_RBP_ID_15777990,Human_RBP_ID_18072603,Human_RBP_ID_18539902,Human_RBP_ID_18861789,Human_RBP_ID_21319045,Human_RBP_ID_22513885,Human_RBP_ID_22830871,Human_RBP_ID_23138663,Human_RBP_ID_24155380,Human_RBP_ID_24435560,Human_RBP_ID_24513966,Human_RBP_ID_26714537,Human_RBP_ID_27344780 68840 RMVar_ID_68840 Human_SNP_ID_271284449 m1A Human chr6 - 28758370 28758370 28758370 GCATGTGTGAGGCCCCGGGTTCGATCCCCGGCACCTCCAAATGGTGGTTTTGCTCTGGCAGTGCT GCATGTGTGAGGCCCCGGGTTCGATCCCCGGCCCCTCCAAATGGTGGTTTTGCTCTGGCAGTGCT T G tRNA-Ala-TGC-6-1,piR-49039 RNACentral:URS00006C133C,RNACentral:URS000000AA0C tRNA,piRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28758322..28758419 26863196 MeRIP-seq:(Medium) rs898537853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660267,Human_RBP_ID_1046456,Human_RBP_ID_1679108,Human_RBP_ID_2017538,Human_RBP_ID_3805292,Human_RBP_ID_4910681,Human_RBP_ID_5428328,Human_RBP_ID_5451007,Human_RBP_ID_7589183,Human_RBP_ID_8270023,Human_RBP_ID_8641089,Human_RBP_ID_15777990,Human_RBP_ID_18072603,Human_RBP_ID_18539902,Human_RBP_ID_18861789,Human_RBP_ID_21319045,Human_RBP_ID_22513885,Human_RBP_ID_22830871,Human_RBP_ID_23138663,Human_RBP_ID_24155380,Human_RBP_ID_24435560,Human_RBP_ID_24513966,Human_RBP_ID_26714537,Human_RBP_ID_27344780 68841 RMVar_ID_68841 Human_SNP_ID_271284476 m1A Human chr6 + 28758408 28758408 28758408 GGATCGAACCCGGGGCCTCACACATGCAAAGCATGTGCTCTACCACTGAGCTACACCCCCCTCCT GGATCGAACCCGGGGCCTCACACATGCAAAGCGTGTGCTCTACCACTGAGCTACACCCCCCTCCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:28758298..28758426 26863196 MeRIP-seq:(Medium) rs1344900961 Functional Loss SNV dbSNP153 33..33 33 - - - 68842 RMVar_ID_68842 Human_SNP_ID_271293340 m1A Human chr6 - 28789785 28789785 28789785 GCATGCTTTGCATGTATGAGGTCCCGGGTTCGATCCCCGGCACCTCCAAACGGTGACTTTTTGCT GCATGCTTTGCATGTATGAGGTCCCGGGTTCGGTCCCCGGCACCTCCAAACGGTGACTTTTTGCT T C tRNA-Ala-TGC-1-1,TRA-TGC1-1 RNACentral:URS00006C6D0A,RNACentral:URS0000679BF3 tRNA,tRNA exon,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs897034291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284938,Human_RBP_ID_1216965,Human_RBP_ID_1326682,Human_RBP_ID_1394918,Human_RBP_ID_1669903,Human_RBP_ID_2017543,Human_RBP_ID_5511281,Human_RBP_ID_7589193,Human_RBP_ID_8270027,Human_RBP_ID_8641097,Human_RBP_ID_9193189,Human_RBP_ID_18086871,Human_RBP_ID_18450037,Human_RBP_ID_18861803,Human_RBP_ID_22830873,Human_RBP_ID_23138682,Human_RBP_ID_24155385 68843 RMVar_ID_68843 Human_SNP_ID_271293811 m1A Human chr6 - 28790737 28790737 28790737 GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCAGGGTTTTTTTTTTTTCT GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGGTCCCGGGTTTCGGCAGGGTTTTTTTTTTTTCT T C TRF-GAA1-1,TRF-GAA1-1:2,TRF-GAA1-1:3,TRF-GAA1-1:4,tRNA-Phe-GAA-1-3 RNACentral:URS0000632456,RNACentral:URS00001CE4E0,RNACentral:URS00006A7E04,RNACentral:URS00006D05AC,RNACentral:URS000029CCC5 tRNA,tRNA,tRNA,tRNA,tRNA intron,intron,intron,intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1329772390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669905,Human_RBP_ID_5477934,Human_RBP_ID_7589195,Human_RBP_ID_8270029,Human_RBP_ID_8641101,Human_RBP_ID_17423205,Human_RBP_ID_18861806,Human_RBP_ID_23138686,Human_RBP_ID_24155388 68844 RMVar_ID_68844 Human_SNP_ID_271297214 m1A Human chr6 + 28802803 28802803 28802803 TTGAGAACTGCCAGAGGGAAACCATCACTTGGAGGTGTCGGGGATCGAACCGAGGCCTCATACAT TTGAGAACTGCCAGAGGGAAACCATCACTTGGTGGTGTCGGGGATCGAACCGAGGCCTCATACAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28802771..28802837 26863196 MeRIP-seq:(Medium) rs796292052 Functional Loss SNV dbSNP153 33..33 33 - - - 68845 RMVar_ID_68845 Human_SNP_ID_271299680 m1A Human chr6 - 28812108 28812108 28812108 GGTATAGCTCAGCGGTAGAGCGCGTGCTTAGCATGCACGAGGTCCTGGGTTCAATCCCCAATACC GGTATAGCTCAGCGGTAGAGCGCGTGCTTAGCGTGCACGAGGTCCTGGGTTCAATCCCCAATACC T C lnc-TRIM27-18,TRA-AGC6-1,tRNA-Ala-AGC-6-1 RNACentral:URS00008BABD2,RNACentral:URS00006AF484,RNACentral:URS000071E903 lincRNA,tRNA,tRNA intron,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1250874261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284942,Human_RBP_ID_660281,Human_RBP_ID_1046463,Human_RBP_ID_1216978,Human_RBP_ID_1679119,Human_RBP_ID_2017555,Human_RBP_ID_3805307,Human_RBP_ID_5219162,Human_RBP_ID_5269088,Human_RBP_ID_5511290,Human_RBP_ID_5536143,Human_RBP_ID_7589221,Human_RBP_ID_8270041,Human_RBP_ID_8641116,Human_RBP_ID_8899522,Human_RBP_ID_15778038,Human_RBP_ID_17041965,Human_RBP_ID_17711702,Human_RBP_ID_18086874,Human_RBP_ID_18519241,Human_RBP_ID_18861823,Human_RBP_ID_21319079,Human_RBP_ID_22102677,Human_RBP_ID_22310165,Human_RBP_ID_22513892,Human_RBP_ID_22830882,Human_RBP_ID_23068770,Human_RBP_ID_23138710,Human_RBP_ID_24155402,Human_RBP_ID_24437455,Human_RBP_ID_24512073,Human_RBP_ID_26041074,Human_RBP_ID_26534914,Human_RBP_ID_26714541,Human_RBP_ID_27094771,Human_RBP_ID_27344797,Human_RBP_ID_27522556,Human_RBP_ID_27568296,Human_RBP_ID_27754620 68846 RMVar_ID_68846 Human_SNP_ID_271299681 m1A Human chr6 - 28812108 28812108 28812108 GGTATAGCTCAGCGGTAGAGCGCGTGCTTAGCATGCACGAGGTCCTGGGTTCAATCCCCAATACC GGTATAGCTCAGCGGTAGAGCGCGTGCTTAGCCTGCACGAGGTCCTGGGTTCAATCCCCAATACC T G lnc-TRIM27-18,TRA-AGC6-1,tRNA-Ala-AGC-6-1 RNACentral:URS00008BABD2,RNACentral:URS00006AF484,RNACentral:URS000071E903 lincRNA,tRNA,tRNA intron,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1250874261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284942,Human_RBP_ID_660281,Human_RBP_ID_1046463,Human_RBP_ID_1216978,Human_RBP_ID_1679119,Human_RBP_ID_2017555,Human_RBP_ID_3805307,Human_RBP_ID_5219162,Human_RBP_ID_5269088,Human_RBP_ID_5511290,Human_RBP_ID_5536143,Human_RBP_ID_7589221,Human_RBP_ID_8270041,Human_RBP_ID_8641116,Human_RBP_ID_8899522,Human_RBP_ID_15778038,Human_RBP_ID_17041965,Human_RBP_ID_17711702,Human_RBP_ID_18086874,Human_RBP_ID_18519241,Human_RBP_ID_18861823,Human_RBP_ID_21319079,Human_RBP_ID_22102677,Human_RBP_ID_22310165,Human_RBP_ID_22513892,Human_RBP_ID_22830882,Human_RBP_ID_23068770,Human_RBP_ID_23138710,Human_RBP_ID_24155402,Human_RBP_ID_24437455,Human_RBP_ID_24512073,Human_RBP_ID_26041074,Human_RBP_ID_26534914,Human_RBP_ID_26714541,Human_RBP_ID_27094771,Human_RBP_ID_27344797,Human_RBP_ID_27522556,Human_RBP_ID_27568296,Human_RBP_ID_27754620 68847 RMVar_ID_68847 Human_SNP_ID_271312473 m1A Human chr6 - 28863700 28863700 28863700 GCGTGCTTAGCATGCACGAGGCCCCGGGTTCAATCCCCGGCACCTCCAGCTTCATTTTTCTCCCG GCGTGCTTAGCATGCACGAGGCCCCGGGTTCAGTCCCCGGCACCTCCAGCTTCATTTTTCTCCCG T C LINC01623 Ensembl:ENSG00000225595 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs766856374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12930,Human_RBP_ID_284947,Human_RBP_ID_660291,Human_RBP_ID_1679127,Human_RBP_ID_5428336,Human_RBP_ID_5477944,Human_RBP_ID_5511297,Human_RBP_ID_7589234,Human_RBP_ID_8271546,Human_RBP_ID_8641130,Human_RBP_ID_8899532,Human_RBP_ID_15935836,Human_RBP_ID_17164338,Human_RBP_ID_17423195,Human_RBP_ID_17710369,Human_RBP_ID_18086462,Human_RBP_ID_18450047,Human_RBP_ID_18545667,Human_RBP_ID_18861842,Human_RBP_ID_21319091,Human_RBP_ID_22830892,Human_RBP_ID_23067991,Human_RBP_ID_23116565,Human_RBP_ID_23138735,Human_RBP_ID_24155412,Human_RBP_ID_24536464,Human_RBP_ID_26764367,Human_RBP_ID_26771893 68848 RMVar_ID_68848 Human_SNP_ID_271312474 m1A Human chr6 - 28863700 28863700 28863700 GCGTGCTTAGCATGCACGAGGCCCCGGGTTCAATCCCCGGCACCTCCAGCTTCATTTTTCTCCCG GCGTGCTTAGCATGCACGAGGCCCCGGGTTCACTCCCCGGCACCTCCAGCTTCATTTTTCTCCCG T G LINC01623 Ensembl:ENSG00000225595 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs766856374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12930,Human_RBP_ID_284947,Human_RBP_ID_660291,Human_RBP_ID_1679127,Human_RBP_ID_5428336,Human_RBP_ID_5477944,Human_RBP_ID_5511297,Human_RBP_ID_7589234,Human_RBP_ID_8271546,Human_RBP_ID_8641130,Human_RBP_ID_8899532,Human_RBP_ID_15935836,Human_RBP_ID_17164338,Human_RBP_ID_17423195,Human_RBP_ID_17710369,Human_RBP_ID_18086462,Human_RBP_ID_18450047,Human_RBP_ID_18545667,Human_RBP_ID_18861842,Human_RBP_ID_21319091,Human_RBP_ID_22830892,Human_RBP_ID_23067991,Human_RBP_ID_23116565,Human_RBP_ID_23138735,Human_RBP_ID_24155412,Human_RBP_ID_24536464,Human_RBP_ID_26764367,Human_RBP_ID_26771893 68849 RMVar_ID_68849 Human_SNP_ID_271323789 m1A Human chr6 + 28896273 28896273 28896273 AACCCACGCCTCCATTGGAGACCAGAATCCCCACCGCGGAGGAAGCTTAGCTTGAGTCTGGCGCC AACCCACGCCTCCATTGGAGACCAGAATCCCCGCCGCGGAGGAAGCTTAGCTTGAGTCTGGCGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr6:28896185..28896325;chr6:28896182..28896325 26863196 MeRIP-seq:(Medium) rs1424486333 Functional Loss SNV dbSNP153 33..33 33 - - - 68850 RMVar_ID_68850 Human_SNP_ID_271323809 m1A Human chr6 - 28896287 28896287 28896287 GCCGAGTGGTCTAAGGCGCCAGACTCAAGCTAAGCTTCCTCCGCGGTGGGGATTCTGGTCTCCAA GCCGAGTGGTCTAAGGCGCCAGACTCAAGCTAGGCTTCCTCCGCGGTGGGGATTCTGGTCTCCAA T C TRL-CAA1-1-001,tRNA-Leu,tRNA-Leu:2,tRNA-Leu-CAA-1-1,TRL-CAA1-1-001:2 RNACentral:URS0000224A3A,RNACentral:URS00004AEFEF,RNACentral:URS000044259A,RNACentral:URS0000747665,RNACentral:URS000071E759 tRNA,tRNA,tRNA,tRNA,tRNA intron,intron,intron,intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:28896203..28896357 26863196 MeRIP-seq:(Medium) rs1358654044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660302,Human_RBP_ID_1216994,Human_RBP_ID_1245649,Human_RBP_ID_1394941,Human_RBP_ID_1669933,Human_RBP_ID_2017568,Human_RBP_ID_3001980,Human_RBP_ID_3805315,Human_RBP_ID_4878077,Human_RBP_ID_5622217,Human_RBP_ID_7589240,Human_RBP_ID_8270050,Human_RBP_ID_8641139,Human_RBP_ID_8899538,Human_RBP_ID_9193200,Human_RBP_ID_15778064,Human_RBP_ID_17092154,Human_RBP_ID_17306216,Human_RBP_ID_17710372,Human_RBP_ID_18072630,Human_RBP_ID_18369887,Human_RBP_ID_18450049,Human_RBP_ID_18519246,Human_RBP_ID_18539025,Human_RBP_ID_18861853,Human_RBP_ID_21319103,Human_RBP_ID_22830900,Human_RBP_ID_23110818,Human_RBP_ID_23138746,Human_RBP_ID_24179882,Human_RBP_ID_24513771,Human_RBP_ID_26534919,Human_RBP_ID_26714547,Human_RBP_ID_27161048,Human_RBP_ID_27344808,Human_RBP_ID_27754628 68851 RMVar_ID_68851 Human_SNP_ID_271323811 m1A Human chr6 - 28896288 28896288 28896288 GGCCGAGTGGTCTAAGGCGCCAGACTCAAGCTAAGCTTCCTCCGCGGTGGGGATTCTGGTCTCCA GGCCGAGTGGTCTAAGGCGCCAGACTCAAGCTGAGCTTCCTCCGCGGTGGGGATTCTGGTCTCCA T C TRL-CAA1-1-001,tRNA-Leu,tRNA-Leu:2,tRNA-Leu-CAA-1-1,TRL-CAA1-1-001:2 RNACentral:URS0000224A3A,RNACentral:URS00004AEFEF,RNACentral:URS000044259A,RNACentral:URS0000747665,RNACentral:URS000071E759 tRNA,tRNA,tRNA,tRNA,tRNA intron,intron,intron,intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:28896223..28896352 26863196 MeRIP-seq:(Medium) rs1024578421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660302,Human_RBP_ID_1216994,Human_RBP_ID_1245649,Human_RBP_ID_1394941,Human_RBP_ID_1669933,Human_RBP_ID_2017568,Human_RBP_ID_3001980,Human_RBP_ID_3805315,Human_RBP_ID_4878077,Human_RBP_ID_5622217,Human_RBP_ID_7589240,Human_RBP_ID_8270050,Human_RBP_ID_8641139,Human_RBP_ID_8899538,Human_RBP_ID_9193200,Human_RBP_ID_15778064,Human_RBP_ID_17306216,Human_RBP_ID_18072630,Human_RBP_ID_18369887,Human_RBP_ID_18450049,Human_RBP_ID_18519246,Human_RBP_ID_18539025,Human_RBP_ID_18861853,Human_RBP_ID_21319103,Human_RBP_ID_22830900,Human_RBP_ID_23110818,Human_RBP_ID_23138746,Human_RBP_ID_24179882,Human_RBP_ID_24513771,Human_RBP_ID_26534919,Human_RBP_ID_26714547,Human_RBP_ID_27161048,Human_RBP_ID_27344808,Human_RBP_ID_27754628 68852 RMVar_ID_68852 Human_SNP_ID_271330178 m1A Human chr6 - 28920119 28920119 28920119 GCCTTGAGGAGCTAGACTTGGCCATCTACAATAGCATCAATGGTGCCATCACCCAGTTCTCTTGC GCCTTGAGGAGCTAGACTTGGCCATCTACAATCGCATCAATGGTGCCATCACCCAGTTCTCTTGC T G TRIM27 Ensembl:ENSG00000204713 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:28920069..28920183 26863196 MeRIP-seq:(Medium) rs1176227163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9400156,Human_RBP_ID_21319206,Human_RBP_ID_23116491 RMVar_hsa_circ_15709 68853 RMVar_ID_68853 Human_SNP_ID_271335457 m1A Human chr6 + 28941109 28941109 28941109 GCGCCAGACTCAAGCTTGGCTTCCTCGTGTTGAGGATTCTGGTCTCCAATGGAGGCGTGGGTTCG GCGCCAGACTCAAGCTTGGCTTCCTCGTGTTGGGGATTCTGGTCTCCAATGGAGGCGTGGGTTCG A G lnc-OR2J1-12,TRL-CAA1-2,TRL-CAA1-1-001,tRNA-Leu,tRNA-Leu:2,tRNA-Leu:3,TRL-CAA1-2:2,tRNA-Leu-CAA-1-1 RNACentral:URS00008B9727,RNACentral:URS00006F4B95,RNACentral:URS0000224A3A,RNACentral:URS0000549EAC,RNACentral:URS00004AEFEF,RNACentral:URS000044259A,RNACentral:URS000047F3CB,RNACentral:URS0000747665 lincRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA,tRNA exon,exon,intron,intron,intron,intron,intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:28941053..28941174 26863196 MeRIP-seq:(Medium) rs191229167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660358,Human_RBP_ID_1217002,Human_RBP_ID_1394945,Human_RBP_ID_1669987,Human_RBP_ID_2017646,Human_RBP_ID_3002045,Human_RBP_ID_3805367,Human_RBP_ID_4910745,Human_RBP_ID_5268487,Human_RBP_ID_5276784,Human_RBP_ID_5617713,Human_RBP_ID_7589444,Human_RBP_ID_8270058,Human_RBP_ID_8641197,Human_RBP_ID_8899558,Human_RBP_ID_15778674,Human_RBP_ID_18072667,Human_RBP_ID_18211235,Human_RBP_ID_18369897,Human_RBP_ID_18861913,Human_RBP_ID_21221546,Human_RBP_ID_22310255,Human_RBP_ID_22830922,Human_RBP_ID_23068782,Human_RBP_ID_23110812,Human_RBP_ID_23138749,Human_RBP_ID_24155495,Human_RBP_ID_26534934,Human_RBP_ID_27094850,Human_RBP_ID_27344840,Human_RBP_ID_27754649 68854 RMVar_ID_68854 Human_SNP_ID_271335462 m1A Human chr6 - 28941113 28941113 28941113 GATTCGAACCCACGCCTCCATTGGAGACCAGAATCCTCAACACGAGGAAGCCAAGCTTGAGTCTG GATTCGAACCCACGCCTCCATTGGAGACCAGAGTCCTCAACACGAGGAAGCCAAGCTTGAGTCTG T C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:28941051..28941200 26863196 MeRIP-seq:(Medium) rs1364796897 Functional Loss SNV dbSNP153 33..33 33 - - - 68855 RMVar_ID_68855 Human_SNP_ID_271335463 m1A Human chr6 - 28941114 28941114 28941114 GGATTCGAACCCACGCCTCCATTGGAGACCAGAATCCTCAACACGAGGAAGCCAAGCTTGAGTCT GGATTCGAACCCACGCCTCCATTGGAGACCAGGATCCTCAACACGAGGAAGCCAAGCTTGAGTCT T C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:28941051..28941125 26863196 MeRIP-seq:(Medium) rs1007372444 Functional Loss SNV dbSNP153 33..33 33 - - - 68856 RMVar_ID_68856 Human_SNP_ID_271335464 m1A Human chr6 - 28941114 28941114 28941114 GGATTCGAACCCACGCCTCCATTGGAGACCAGAATCCTCAACACGAGGAAGCCAAGCTTGAGTCT GGATTCGAACCCACGCCTCCATTGGAGACCAGCATCCTCAACACGAGGAAGCCAAGCTTGAGTCT T G RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:28941051..28941125 26863196 MeRIP-seq:(Medium) rs1007372444 Functional Loss SNV dbSNP153 33..33 33 - - - 68857 RMVar_ID_68857 Human_SNP_ID_271336198 m1A Human chr6 - 28943637 28943637 28943637 AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGAATCCCACCGCTGCCAGTGTGAGGTATTTTTTT AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGGATCCCACCGCTGCCAGTGTGAGGTATTTTTTT T C tRNA-Leu-AAG-2-3,RF00017-4692 RNACentral:URS0000120E41,RNACentral:URS000090D53C tRNA,SRP RNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1422870518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1669996,Human_RBP_ID_8641207,Human_RBP_ID_10279065,Human_RBP_ID_17092153,Human_RBP_ID_18174238,Human_RBP_ID_21319244,Human_RBP_ID_22830929,Human_RBP_ID_23059471,Human_RBP_ID_23138756 68858 RMVar_ID_68858 Human_SNP_ID_271339063 m1A Human chr6 + 28951042 28951039 28951043 AAGAAGGCTTTTGCAGGGAGCCCGGATAGCTCAGTCGGTAGAGCATCAGACTTTTAATCTGAGGG AAGAAGGCTTTTGCAGGGAGCCCGGATAGC____TCGGTAGAGCATCAGACTTTTAATCTGAGGG CTCAG C TRK1,TRK-TTT3-1,JX944780,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS0000D4B79F,RNACentral:URS000022DD4A tRNA,tRNA,precursor RNA,tRNA exon,exon,exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:28951023..28951108 26863410 MeRIP-seq:(Medium) rs1447874603 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_1679138,Human_RBP_ID_2017653,Human_RBP_ID_3805372,Human_RBP_ID_5216263,Human_RBP_ID_5428347,Human_RBP_ID_5511311,Human_RBP_ID_7589461,Human_RBP_ID_8641214,Human_RBP_ID_10279068,Human_RBP_ID_15778693,Human_RBP_ID_17044970,Human_RBP_ID_18202644,Human_RBP_ID_18211236,Human_RBP_ID_18861928,Human_RBP_ID_21319248,Human_RBP_ID_21950330,Human_RBP_ID_22830932,Human_RBP_ID_23110814,Human_RBP_ID_23112057,Human_RBP_ID_23116598,Human_RBP_ID_23138767,Human_RBP_ID_26751495,Human_RBP_ID_27102702,Human_RBP_ID_27344844 68859 RMVar_ID_68859 Human_SNP_ID_271339106 m1A Human chr6 - 28951069 28951069 28951069 CGCCCGAACAGGGACTTGAACCCTGGACCCTCAGATTAAAAGTCTGATGCTCTACCGACTGAGCT CGCCCGAACAGGGACTTGAACCCTGGACCCTCGGATTAAAAGTCTGATGCTCTACCGACTGAGCT T C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:28951027..28951123 26863410 MeRIP-seq:(Medium) rs548650448 Functional Loss SNV dbSNP153 33..33 33 - - - 68860 RMVar_ID_68860 Human_SNP_ID_271339107 m1A Human chr6 - 28951069 28951069 28951069 CGCCCGAACAGGGACTTGAACCCTGGACCCTCAGATTAAAAGTCTGATGCTCTACCGACTGAGCT CGCCCGAACAGGGACTTGAACCCTGGACCCTCCGATTAAAAGTCTGATGCTCTACCGACTGAGCT T G RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:28951027..28951123 26863410 MeRIP-seq:(Medium) rs548650448 Functional Loss SNV dbSNP153 33..33 33 - - - 68861 RMVar_ID_68861 Human_SNP_ID_271339128 m1A Human chr6 + 28951085 28951085 28951085 CATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTA CATCAGACTTTTAATCTGAGGGTCCAGGGTTCCAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTA A C TRK1,TRK-TTT3-1,JX944780,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS0000D4B79F,RNACentral:URS000022DD4A tRNA,tRNA,precursor RNA,tRNA exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1226467066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270930,Human_RBP_ID_1142396,Human_RBP_ID_1217010,Human_RBP_ID_1670006,Human_RBP_ID_2017656,Human_RBP_ID_4878206,Human_RBP_ID_5219168,Human_RBP_ID_5268492,Human_RBP_ID_5477960,Human_RBP_ID_5511312,Human_RBP_ID_7589464,Human_RBP_ID_8270064,Human_RBP_ID_8641217,Human_RBP_ID_9193209,Human_RBP_ID_10313214,Human_RBP_ID_15778698,Human_RBP_ID_17045144,Human_RBP_ID_17423064,Human_RBP_ID_18202645,Human_RBP_ID_18861930,Human_RBP_ID_21319248,Human_RBP_ID_22310268,Human_RBP_ID_22830932,Human_RBP_ID_23059475,Human_RBP_ID_23138770,Human_RBP_ID_23293917,Human_RBP_ID_24155510,Human_RBP_ID_24435569,Human_RBP_ID_24512084,Human_RBP_ID_25993939,Human_RBP_ID_26534940,Human_RBP_ID_27094859,Human_RBP_ID_27161320 68862 RMVar_ID_68862 Human_SNP_ID_271339129 m1A Human chr6 + 28951086 28951086 28951086 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAG ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAGGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAG A G RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs113225886 Functional Loss SNV dbSNP153 33..33 33 - - - 68863 RMVar_ID_68863 Human_SNP_ID_271339130 m1A Human chr6 + 28951086 28951086 28951086 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAG ATCAGACTTTTAATCTGAGGGTCCAGGGTTCATGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAG A T RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs113225886 Functional Loss SNV dbSNP153 33..33 33 - - - 68864 RMVar_ID_68864 Human_SNP_ID_271339161 m1A Human chr6 + 28951104 28951104 28951104 GGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAGTACCTGATTCTGGTATCA GGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGGGTGGTGGCTTTTAGTACCTGATTCTGGTATCA A G JX944780,JX944780:2 RNACentral:URS0000D4B79F,RNACentral:URS00002CDFCA precursor RNA,miRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr6:28951039..28951122;chr6:28950978..28951125 26863196 MeRIP-seq:(Medium) rs529570811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046490,Human_RBP_ID_1217011,Human_RBP_ID_1245651,Human_RBP_ID_1670006,Human_RBP_ID_2017656,Human_RBP_ID_5268493,Human_RBP_ID_5276786,Human_RBP_ID_5451028,Human_RBP_ID_5477961,Human_RBP_ID_5511313,Human_RBP_ID_7589465,Human_RBP_ID_8270065,Human_RBP_ID_8641218,Human_RBP_ID_8899564,Human_RBP_ID_9193209,Human_RBP_ID_15778698,Human_RBP_ID_17041977,Human_RBP_ID_17419400,Human_RBP_ID_18072673,Human_RBP_ID_18450052,Human_RBP_ID_18861931,Human_RBP_ID_21319252,Human_RBP_ID_23138771,Human_RBP_ID_23293918,Human_RBP_ID_24155510,Human_RBP_ID_27161321 68865 RMVar_ID_68865 Human_SNP_ID_271339162 m1A Human chr6 + 28951104 28951104 28951104 GGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGAGTGGTGGCTTTTAGTACCTGATTCTGGTATCA GGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGGTGTGGTGGCTTTTAGTACCTGATTCTGGTATCA A T JX944780,JX944780:2 RNACentral:URS0000D4B79F,RNACentral:URS00002CDFCA precursor RNA,miRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr6:28951039..28951122;chr6:28950978..28951125 26863196 MeRIP-seq:(Medium) rs529570811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046490,Human_RBP_ID_1217011,Human_RBP_ID_1245651,Human_RBP_ID_1670006,Human_RBP_ID_2017656,Human_RBP_ID_5268493,Human_RBP_ID_5276786,Human_RBP_ID_5451028,Human_RBP_ID_5477961,Human_RBP_ID_5511313,Human_RBP_ID_7589465,Human_RBP_ID_8270065,Human_RBP_ID_8641218,Human_RBP_ID_8899564,Human_RBP_ID_9193209,Human_RBP_ID_15778698,Human_RBP_ID_17041977,Human_RBP_ID_17419400,Human_RBP_ID_18072673,Human_RBP_ID_18450052,Human_RBP_ID_18861931,Human_RBP_ID_21319252,Human_RBP_ID_23138771,Human_RBP_ID_23293918,Human_RBP_ID_24155510,Human_RBP_ID_27161321 68866 RMVar_ID_68866 Human_SNP_ID_271339855 m1A Human chr6 - 28953280 28953280 28953280 GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGAACCTCAGAGGGGGCAGCTGCCATTTTGTCCCC GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGTACCTCAGAGGGGGCAGCTGCCATTTTGTCCCC T A TRM-CAT3-1,tRNA-Met-CAT-3-1,RF00017-4692 RNACentral:URS000062A60A,RNACentral:URS000025E031,RNACentral:URS000090D53C tRNA,tRNA,SRP RNA exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1033918219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284956,Human_RBP_ID_1217014,Human_RBP_ID_1394949,Human_RBP_ID_1670009,Human_RBP_ID_2017657,Human_RBP_ID_3805374,Human_RBP_ID_5251112,Human_RBP_ID_5268495,Human_RBP_ID_5477964,Human_RBP_ID_5511315,Human_RBP_ID_7589470,Human_RBP_ID_8270067,Human_RBP_ID_8641221,Human_RBP_ID_8899567,Human_RBP_ID_9193210,Human_RBP_ID_10313216,Human_RBP_ID_15778703,Human_RBP_ID_17041980,Human_RBP_ID_17535401,Human_RBP_ID_17585216,Human_RBP_ID_17710381,Human_RBP_ID_18072675,Human_RBP_ID_18450054,Human_RBP_ID_18861934,Human_RBP_ID_21319256,Human_RBP_ID_21950338,Human_RBP_ID_22102717,Human_RBP_ID_22310271,Human_RBP_ID_22513902,Human_RBP_ID_22830933,Human_RBP_ID_23138778,Human_RBP_ID_24155512,Human_RBP_ID_24435571,Human_RBP_ID_24513731,Human_RBP_ID_26041072,Human_RBP_ID_26714568,Human_RBP_ID_27094861,Human_RBP_ID_27522615,Human_RBP_ID_27568303 68867 RMVar_ID_68867 Human_SNP_ID_271339856 m1A Human chr6 - 28953280 28953280 28953280 GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGAACCTCAGAGGGGGCAGCTGCCATTTTGTCCCC GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGGACCTCAGAGGGGGCAGCTGCCATTTTGTCCCC T C TRM-CAT3-1,tRNA-Met-CAT-3-1,RF00017-4692 RNACentral:URS000062A60A,RNACentral:URS000025E031,RNACentral:URS000090D53C tRNA,tRNA,SRP RNA exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1033918219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284956,Human_RBP_ID_1217014,Human_RBP_ID_1394949,Human_RBP_ID_1670009,Human_RBP_ID_2017657,Human_RBP_ID_3805374,Human_RBP_ID_5251112,Human_RBP_ID_5268495,Human_RBP_ID_5477964,Human_RBP_ID_5511315,Human_RBP_ID_7589470,Human_RBP_ID_8270067,Human_RBP_ID_8641221,Human_RBP_ID_8899567,Human_RBP_ID_9193210,Human_RBP_ID_10313216,Human_RBP_ID_15778703,Human_RBP_ID_17041980,Human_RBP_ID_17535401,Human_RBP_ID_17585216,Human_RBP_ID_17710381,Human_RBP_ID_18072675,Human_RBP_ID_18450054,Human_RBP_ID_18861934,Human_RBP_ID_21319256,Human_RBP_ID_21950338,Human_RBP_ID_22102717,Human_RBP_ID_22310271,Human_RBP_ID_22513902,Human_RBP_ID_22830933,Human_RBP_ID_23138778,Human_RBP_ID_24155512,Human_RBP_ID_24435571,Human_RBP_ID_24513731,Human_RBP_ID_26041072,Human_RBP_ID_26714568,Human_RBP_ID_27094861,Human_RBP_ID_27522615,Human_RBP_ID_27568303 68868 RMVar_ID_68868 Human_SNP_ID_271347981 m1A Human chr6 + 28982255 28982255 28982255 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAATGAGGTTTTTCTGTTTT TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGGTTCCCGGTCAGGGAATGAGGTTTTTCTGTTTT A G RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs781327228 Functional Loss SNV dbSNP153 33..33 33 - - - 68869 RMVar_ID_68869 Human_SNP_ID_271347982 m1A Human chr6 + 28982255 28982255 28982255 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAATGAGGTTTTTCTGTTTT TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGTTTCCCGGTCAGGGAATGAGGTTTTTCTGTTTT A T RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs781327228 Functional Loss SNV dbSNP153 33..33 33 - - - 68870 RMVar_ID_68870 Human_SNP_ID_271349833 m1A Human chr6 + 28989067 28989067 28989067 TAAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCAAATCCCACCGCTGCCAAGTACTTTTCATTCTC TAAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGAATCCCACCGCTGCCAAGTACTTTTCATTCTC A G tRNA-Leu-AAG-3-1 RNACentral:URS000064506B tRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs935729417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660368,Human_RBP_ID_1245653,Human_RBP_ID_1326705,Human_RBP_ID_5477968,Human_RBP_ID_8270074,Human_RBP_ID_9193214,Human_RBP_ID_23138799 68871 RMVar_ID_68871 Human_SNP_ID_271349835 m1A Human chr6 + 28989068 28989068 28989068 AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCAAATCCCACCGCTGCCAAGTACTTTTCATTCTCA AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCACATCCCACCGCTGCCAAGTACTTTTCATTCTCA A C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs919246978 Functional Loss SNV dbSNP153 33..33 33 - - - 68872 RMVar_ID_68872 Human_SNP_ID_271349871 m1A Human chr6 + 28989132 28989132 28989132 ACTAGGGACTGTTTTTAGGAGAATCCCTTTCCAAATGTTCAGTATGAATGGTTCTTACGTATCAA ACTAGGGACTGTTTTTAGGAGAATCCCTTTCCGAATGTTCAGTATGAATGGTTCTTACGTATCAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:28989081..28989233 26863196 MeRIP-seq:(Medium) rs1329559025 Functional Loss SNV dbSNP153 33..33 33 - - - 68873 RMVar_ID_68873 Human_SNP_ID_271488409 m1A Human chr6 - 29624181 29624181 29624181 AGTTTAATGAAAGAGGAGAAAAAAGGCACTTGACAGGAAGAGATGCCAGAAAGGAGAAGAAAACG AGTTTAATGAAAGAGGAGAAAAAAGGCACTTGTCAGGAAGAGATGCCAGAAAGGAGAAGAAAACG T A GABBR1 Ensembl:ENSG00000204681 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29624131..29624270 26863196 MeRIP-seq:(Medium) rs1331180601 Functional Loss SNV dbSNP153 33..33 33 - - - 68874 RMVar_ID_68874 Human_SNP_ID_271489277 m1A Human chr6 + 29628203 29628203 29628203 CGACAGTCGGAGGGGCGGGGAGGGGAGGGGGGATGCAACCTCGAGGAGGAAAGGAACGAAAGAGG CGACAGTCGGAGGGGCGGGGAGGGGAGGGGGGGTGCAACCTCGAGGAGGAAAGGAACGAAAGAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:29628198..29628315 32194978 MeRIP-seq:(Medium) rs1260771859 Functional Loss SNV dbSNP153 33..33 33 - - - 68875 RMVar_ID_68875 Human_SNP_ID_271489289 m1A Human chr6 + 29628314 29628268 29628314 GACGGGGCGTGCCAGGAGGGCGGGGTGGGCGGAGGGAGCCGCGGGAGGCTGAAGCACGGAGGAAC _________________________________GGGAGCCGCGGGAGGCTGAAGCACGGAGGAAC GGAGGAGAAATGGGGACGGGGCGTGCCAGGAGGGCGGGGTGGGCGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:29628185..29628391 26863196 MeRIP-seq:(Medium) rs1408422300 Functional Loss DEL dbSNP153 1..33 33 - - - 68876 RMVar_ID_68876 Human_SNP_ID_271489299 m1A Human chr6 - 29628307 29628307 29628307 CGTGCTTCAGCCTCCCGCGGCTCCCTCCGCCCACCCCGCCCTCCTGGCACGCCCCGTCCCCATTT CGTGCTTCAGCCTCCCGCGGCTCCCTCCGCCCCCCCCGCCCTCCTGGCACGCCCCGTCCCCATTT T G GABBR1 Ensembl:ENSG00000204681 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29627853..29628594 26863196 MeRIP-seq:(Medium) rs1377337687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576618 68877 RMVar_ID_68877 Human_SNP_ID_271489318 m1A Human chr6 - 29628372 29628372 29628372 CTCAGGCGCCAGCCCCGTTTCTCTCCCGTCCCACTCGCATCCTTCCCTTCCTACCCTGGTTCCTC CTCAGGCGCCAGCCCCGTTTCTCTCCCGTCCCGCTCGCATCCTTCCCTTCCTACCCTGGTTCCTC T C GABBR1 Ensembl:ENSG00000204681 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:29628298..29628462 26863196 MeRIP-seq:(Medium) rs1259273415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17091111,Human_RBP_ID_21319709 68878 RMVar_ID_68878 Human_SNP_ID_271489320 m1A Human chr6 + 29628376 29628376 29628376 AACCAGGGTAGGAAGGGAAGGATGCGAGTGGGACGGGAGAGAAACGGGGCTGGCGCCTGAGGTCT AACCAGGGTAGGAAGGGAAGGATGCGAGTGGGCCGGGAGAGAAACGGGGCTGGCGCCTGAGGTCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29628331..29628606 26863196 MeRIP-seq:(Medium) rs1203527017 Functional Loss SNV dbSNP153 33..33 33 - - - 68879 RMVar_ID_68879 Human_SNP_ID_271489321 m1A Human chr6 + 29628376 29628376 29628376 AACCAGGGTAGGAAGGGAAGGATGCGAGTGGGACGGGAGAGAAACGGGGCTGGCGCCTGAGGTCT AACCAGGGTAGGAAGGGAAGGATGCGAGTGGGGCGGGAGAGAAACGGGGCTGGCGCCTGAGGTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29628331..29628606 26863196 MeRIP-seq:(Medium) rs1203527017 Functional Loss SNV dbSNP153 33..33 33 - - - 68880 RMVar_ID_68880 Human_SNP_ID_271490217 m1A Human chr6 + 29632289 29632289 29632289 AAGTGGAGCGAAGGAGGGCCGGAGGTCGTCGAAGAAGGATGCACCTTCTGAGGTGGCGTTGGGGG AAGTGGAGCGAAGGAGGGCCGGAGGTCGTCGAGGAAGGATGCACCTTCTGAGGTGGCGTTGGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29632287..29632433 26863196 MeRIP-seq:(Medium) rs78342839 Functional Loss SNV dbSNP153 33..33 33 - - - 68881 RMVar_ID_68881 Human_SNP_ID_271490408 m1A Human chr6 + 29632899 29632899 29632899 GCTCCCCGGCTCTCCCCGGGCCTCAAGGCCCCAGGCCCGGCCGCTCCTCCCCGCTCCCCCCTCCC GCTCCCCGGCTCTCCCCGGGCCTCAAGGCCCCCGGCCCGGCCGCTCCTCCCCGCTCCCCCCTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:29632558..29633124 26863196 MeRIP-seq:(Medium) rs1215244051 Functional Loss SNV dbSNP153 33..33 33 - - - 68882 RMVar_ID_68882 Human_SNP_ID_271490438 m1A Human chr6 - 29632990 29632990 29632990 GGAAGCGAGAGAGGAGGGGAGAGACCCTGGCCAGGCTGGAGCCTGGATTCGAGGGGAGGAGGGAC GGAAGCGAGAGAGGAGGGGAGAGACCCTGGCCGGGCTGGAGCCTGGATTCGAGGGGAGGAGGGAC T C GABBR1 Ensembl:ENSG00000204681 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:29631401..29633132 26863196 MeRIP-seq:(Medium) rs1274724221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252697,Human_RBP_ID_3820742,Human_RBP_ID_3968630,Human_RBP_ID_9437759,Human_RBP_ID_17070033,Human_RBP_ID_21991092,Human_RBP_ID_22618089,Human_RBP_ID_27842586 68883 RMVar_ID_68883 Human_SNP_ID_271512068 m1A Human chr6 + 29723656 29723526 29723656 GGTCTGGCGGGTCTCAGCCCCTCCTCGCCCCCAGGCTCCCACTCCTTGAGGTATTTCAGCACCGC _________________________________GGCTCCCACTCCTTGAGGTATTTCAGCACCGC GGGTGAGTGCGGGGTCCAGAGAGAAACGGCCTCTGTGGGGAGGAGTGAGGGGCCCGCCCGGTGGGGGCGCAGGACTCAGGGAGCCGCCTCCGGAGGAGGGTCTGGCGGGTCTCAGCCCCTCCTCGCCCCCA G HLA-F Ensembl:ENSG00000204642 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29723651..29723851 26863410 MeRIP-seq:(Medium) rs1554225691 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4878338 68884 RMVar_ID_68884 Human_SNP_ID_271512468 m1A Human chr6 + 29724248 29724248 29724248 CGACGGACGCCTCCTCCGCGGGTATCACCAGCACGCGTACGACGGCAAGGATTACATCTCCCTGA CGACGGACGCCTCCTCCGCGGGTATCACCAGCCCGCGTACGACGGCAAGGATTACATCTCCCTGA A C HLA-F Ensembl:ENSG00000204642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:29724198..29724297 26863196 MeRIP-seq:(Medium) rs1455950357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_747564,Human_Splice_Rec_747576,Human_Splice_Rec_747586,Human_Splice_Rec_747598,Human_Splice_Rec_747604,Human_Splice_Rec_747616,Human_Splice_Rec_747624,Human_Splice_Rec_747628 Human_miRNA_ID_273787 68885 RMVar_ID_68885 Human_SNP_ID_271512500 m1A Human chr6 + 29724311 29724311 29724311 GAACGAGGACCTGCGCTCCTGGACCGCGGCGGACACCGTGGCTCAGATCACCCAGCGCTTCTATG GAACGAGGACCTGCGCTCCTGGACCGCGGCGGGCACCGTGGCTCAGATCACCCAGCGCTTCTATG A G HLA-F Ensembl:ENSG00000204642 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29724212..29724312 26863410 MeRIP-seq:(Medium) rs1300515468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_747628 68886 RMVar_ID_68886 Human_SNP_ID_271517459 m1A Human chr6 + 29745352 29745352 29745352 CCATCCCTCCCTGTGTGGGCTGAGCCCCGCTGAGCACCATTCCTCACCCCTACTCACAGCCAAAT CCATCCCTCCCTGTGTGGGCTGAGCCCCGCTGCGCACCATTCCTCACCCCTACTCACAGCCAAAT A C lnc-HLA-F-2 RNACentral:URS00008BFBF4 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:29745345..29745640 26863196 MeRIP-seq:(Medium) rs1231729880 Functional Loss SNV dbSNP153 33..33 33 - - - 68887 RMVar_ID_68887 Human_SNP_ID_271517474 m1A Human chr6 - 29745446 29745446 29745446 AAGGAGGTGAGAGTGGGCAGTGGGCAAGAGTAATGGGAGAGGCCTTTTCCAGGAGAGTTGGGGGC AAGGAGGTGAGAGTGGGCAGTGGGCAAGAGTAGTGGGAGAGGCCTTTTCCAGGAGAGTTGGGGGC T C MICE,HLA-F-AS1 Ensembl:ENSG00000273340,Ensembl:ENSG00000214922 Pseudogene,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:29745440..29745545 26863196 MeRIP-seq:(Medium) rs1486946100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3822382,Human_RBP_ID_9438722,Human_RBP_ID_17092105,Human_RBP_ID_21991991 68888 RMVar_ID_68888 Human_SNP_ID_271518364 m1A Human chr6 + 29748835 29748835 29748835 CCGCCTCGGCCGCACAGCGCTCGCCGCTACCCACCCGGACCCCCAGAAACGCCCCGCCGCTGCCG CCGCCTCGGCCGCACAGCGCTCGCCGCTACCCCCCCGGACCCCCAGAAACGCCCCGCCGCTGCCG A C lnc-HLA-F-2 RNACentral:URS00008BFBF4 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:29748720..29748967 26863196 MeRIP-seq:(Medium) rs1423605367 Functional Loss SNV dbSNP153 33..33 33 - - - 68889 RMVar_ID_68889 Human_SNP_ID_271540749 m1A Human chr6 - 29830428 29830428 29830428 CCAAACACAAGATCCCAAGGATCTCAGGGATCAGCCTCCTTCATACTTACTTGCAGCCTGAGAGT CCAAACACAAGATCCCAAGGATCTCAGGGATCGGCCTCCTTCATACTTACTTGCAGCCTGAGAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:29830425..29830544;chr6:29830425..29830541 26863196 MeRIP-seq:(Medium) rs778879258 Functional Loss SNV dbSNP153 33..33 33 - - - 68890 RMVar_ID_68890 Human_SNP_ID_271557063 m1A Human chr6 + 29887979 29887979 29887979 GCTCCCAGGCTCCCACTCCATGAGGTATTTCTACACCACCATGTCCCGGCCCGGCCGCGGGGAGC GCTCCCAGGCTCCCACTCCATGAGGTATTTCTCCACCACCATGTCCCGGCCCGGCCGCGGGGAGC A C HLA-H Ensembl:ENSG00000206341 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:29887846..29888026;chr6:29887869..29888002 26863196 MeRIP-seq:(Medium) rs1296482776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903145,Human_RBP_ID_22460989 Human_Splice_Rec_747810 68891 RMVar_ID_68891 Human_SNP_ID_271573672 m1A Human chr6 - 29942585 29942577 29942586 TCTGGGTCAGGGCCAGGGCCCCCGAGAGTAGCAGGAGGAGGGTTCGGGGCGCCATGACGGCCATC TCTGGGTCAGGGCCAGGGCCCCCGAGAGTAG_________GGTTCGGGGCGCCATGACGGCCATC CCTCCTCCTG C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:29942526..29942650 26863196 MeRIP-seq:(Medium) rs776873046 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_1678755,Human_RBP_ID_17538248 68892 RMVar_ID_68892 Human_SNP_ID_271573702 m1A Human chr6 + 29942617 29942617 29942617 TGCTACTCTCGGGGGCCCTGGCCCTGACCCAGACCTGGGCGGGTGAGTGCGGGGTCGGGAGGGAA TGCTACTCTCGGGGGCCCTGGCCCTGACCCAGGCCTGGGCGGGTGAGTGCGGGGTCGGGAGGGAA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:29942570..29942670 26863410 MeRIP-seq:(Medium) rs1341761581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791793,Human_RBP_ID_4903147,Human_RBP_ID_5242668,Human_RBP_ID_22460998 Human_Splice_Rec_747839,Human_Splice_Rec_747853,Human_Splice_Rec_747867,Human_Splice_Rec_747881,Human_Splice_Rec_747893,Human_Splice_Rec_747901,Human_Splice_Rec_747913,Human_Splice_Rec_747923,Human_Splice_Rec_747933 68893 RMVar_ID_68893 Human_SNP_ID_271573930 m1A Human chr6 - 29942781 29942779 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTG__GAAATACCTCATGGAGTGGGAGCCTGGGGGC CTT C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs777655287 Functional Loss DEL dbSNP153 33..34 33 - - - 68894 RMVar_ID_68894 Human_SNP_ID_271573933 m1A Human chr6 - 29942781 29942779 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTG_AGAAATACCTCATGGAGTGGGAGCCTGGGGGC CTT CT AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs879903703 Functional Loss DEL dbSNP153 33..33 33 - - - 68895 RMVar_ID_68895 Human_SNP_ID_271573934 m1A Human chr6 - 29942781 29942780 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTGGTGAAATACCTCATGGAGTGGGAGCCTGGGGGC TT AC AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs386698549 Functional Loss MNV dbSNP153 33..34 33 - - - 68896 RMVar_ID_68896 Human_SNP_ID_271573937 m1A Human chr6 - 29942781 29942781 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTGTAGAAATACCTCATGGAGTGGGAGCCTGGGGGC T A AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs2075684 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - 68897 RMVar_ID_68897 Human_SNP_ID_271573938 m1A Human chr6 - 29942781 29942781 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTGGAGAAATACCTCATGGAGTGGGAGCCTGGGGGC T C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs2075684 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 68898 RMVar_ID_68898 Human_SNP_ID_271574003 m1A Human chr6 - 29942819 29942819 29942819 CTGCGTGTCGTCCACGTAGCCCACGGCGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGGACACGG CTGCGTGTCGTCCACGTAGCCCACGGCGATGATGCGGGGCTCCCCGCGGCCGGGCCGGGACACGG T A AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:29942551..29943071 32194978 MeRIP-seq:(Medium) rs199474367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3822769 68899 RMVar_ID_68899 Human_SNP_ID_271574004 m1A Human chr6 - 29942819 29942819 29942819 CTGCGTGTCGTCCACGTAGCCCACGGCGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGGACACGG CTGCGTGTCGTCCACGTAGCCCACGGCGATGAGGCGGGGCTCCCCGCGGCCGGGCCGGGACACGG T C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:29942551..29943071 32194978 MeRIP-seq:(Medium) rs199474367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3822769 68900 RMVar_ID_68900 Human_SNP_ID_271574082 m1A Human chr6 + 29942867 29942867 29942867 ACGTGGACGACACGCAGTTCGTGCGGTTCGACAGCGACGCCGCGAGCCAGAGGATGGAGCCGCGG ACGTGGACGACACGCAGTTCGTGCGGTTCGACGGCGACGCCGCGAGCCAGAGGATGGAGCCGCGG A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:29942757..29942921 26863196 MeRIP-seq:(Medium) rs199474386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82037,Human_RBP_ID_4910809,Human_RBP_ID_22461001,Human_RBP_ID_22773858 68901 RMVar_ID_68901 Human_SNP_ID_271574277 m1A Human chr6 + 29942958 29942958 29942958 GGAGTATTGGGACCAGGAGACACGGAATGTGAAGGCCCAGTCACAGACTGACCGAGTGGACCTGG GGAGTATTGGGACCAGGAGACACGGAATGTGAGGGCCCAGTCACAGACTGACCGAGTGGACCTGG A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:29942751..29943059;chr6:29942501..29943100;chr6:29942501..29943120 26863196 MeRIP-seq:(Medium) rs199474442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18072748 Human_Splice_Rec_747841,Human_Splice_Rec_747855,Human_Splice_Rec_747869,Human_Splice_Rec_747895,Human_Splice_Rec_747915 68902 RMVar_ID_68902 Human_SNP_ID_271574323 m1A Human chr6 + 29942980 29942980 29942980 CGGAATGTGAAGGCCCAGTCACAGACTGACCGAGTGGACCTGGGGACCCTGCGCGGCTACTACAA CGGAATGTGAAGGCCCAGTCACAGACTGACCGCGTGGACCTGGGGACCCTGCGCGGCTACTACAA A C HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29942526..29943078 26863196 MeRIP-seq:(Medium) rs41556115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791796,Human_RBP_ID_2017696,Human_RBP_ID_4878410,Human_RBP_ID_5216268,Human_RBP_ID_8641267,Human_RBP_ID_17710386,Human_RBP_ID_18085721,Human_RBP_ID_18472021,Human_RBP_ID_22461002,Human_RBP_ID_22773325,Human_RBP_ID_26541014,Human_RBP_ID_27161062,Human_RBP_ID_27522644 Human_Splice_Rec_747841,Human_Splice_Rec_747855,Human_Splice_Rec_747869,Human_Splice_Rec_747895,Human_Splice_Rec_747915 68903 RMVar_ID_68903 Human_SNP_ID_271574324 m1A Human chr6 + 29942980 29942980 29942980 CGGAATGTGAAGGCCCAGTCACAGACTGACCGAGTGGACCTGGGGACCCTGCGCGGCTACTACAA CGGAATGTGAAGGCCCAGTCACAGACTGACCGGGTGGACCTGGGGACCCTGCGCGGCTACTACAA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29942526..29943078 26863196 MeRIP-seq:(Medium) rs41556115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791796,Human_RBP_ID_2017696,Human_RBP_ID_4878410,Human_RBP_ID_5216268,Human_RBP_ID_8641267,Human_RBP_ID_17710386,Human_RBP_ID_18085721,Human_RBP_ID_18472021,Human_RBP_ID_22461002,Human_RBP_ID_22773325,Human_RBP_ID_26541014,Human_RBP_ID_27161062,Human_RBP_ID_27522644 Human_Splice_Rec_747841,Human_Splice_Rec_747855,Human_Splice_Rec_747869,Human_Splice_Rec_747895,Human_Splice_Rec_747915 68904 RMVar_ID_68904 Human_SNP_ID_271574617 m1A Human chr6 + 29943274 29943274 29943274 TGGGCTGACCGCGGGGTCGGGGCCAGGTTCTCACACCATCCAGATAATGTATGGCTGCGACGTGG TGGGCTGACCGCGGGGTCGGGGCCAGGTTCTCGCACCATCCAGATAATGTATGGCTGCGACGTGG A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:29943251..29943275 26863196 MeRIP-seq:(Medium) rs199474473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18085723,Human_RBP_ID_22461759,Human_RBP_ID_22553544,Human_RBP_ID_22773328 Human_Splice_Rec_747842,Human_Splice_Rec_747856,Human_Splice_Rec_747870,Human_Splice_Rec_747896,Human_Splice_Rec_747916 68905 RMVar_ID_68905 Human_SNP_ID_271574799 m1A Human chr6 + 29943361 29943361 29943361 CGGGTACCGGCAGGACGCCTACGACGGCAAGGATTACATCGCCCTGAACGAGGACCTGCGCTCTT CGGGTACCGGCAGGACGCCTACGACGGCAAGGTTTACATCGCCCTGAACGAGGACCTGCGCTCTT A T HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:29943251..29943475 26863196 MeRIP-seq:(Medium) rs199474515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3805443 Human_Splice_Rec_747842,Human_Splice_Rec_747856,Human_Splice_Rec_747870,Human_Splice_Rec_747884,Human_Splice_Rec_747896,Human_Splice_Rec_747916 68906 RMVar_ID_68906 Human_SNP_ID_271574800 m1A Human chr6 - 29943362 29943362 29943362 CAAGAGCGCAGGTCCTCGTTCAGGGCGATGTAATCCTTGCCGTCGTAGGCGTCCTGCCGGTACCC CAAGAGCGCAGGTCCTCGTTCAGGGCGATGTACTCCTTGCCGTCGTAGGCGTCCTGCCGGTACCC T G HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:29943251..29944175 32194978 MeRIP-seq:(Medium) rs199474516 Functional Loss SNV dbSNP153 33..33 33 - - - 68907 RMVar_ID_68907 Human_SNP_ID_271574978 m1A Human chr6 + 29943460 29943460 29943460 GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCAGTTGAGAGCCTACCTGGATGGCACGTGCGTGG GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCCGTTGAGAGCCTACCTGGATGGCACGTGCGTGG A C HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:29943188..29943475 26863196 MeRIP-seq:(Medium) rs78674188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4878426,Human_RBP_ID_22405186,Human_RBP_ID_22773331 Human_Splice_Rec_747843,Human_Splice_Rec_747857,Human_Splice_Rec_747871,Human_Splice_Rec_747885,Human_Splice_Rec_747897,Human_Splice_Rec_747903,Human_Splice_Rec_747917,Human_Splice_Rec_747925,Human_Splice_Rec_747935 68908 RMVar_ID_68908 Human_SNP_ID_271574979 m1A Human chr6 + 29943460 29943460 29943460 GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCAGTTGAGAGCCTACCTGGATGGCACGTGCGTGG GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCGGTTGAGAGCCTACCTGGATGGCACGTGCGTGG A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:29943188..29943475 26863196 MeRIP-seq:(Medium) rs78674188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4878426,Human_RBP_ID_22405186,Human_RBP_ID_22773331 Human_Splice_Rec_747843,Human_Splice_Rec_747857,Human_Splice_Rec_747871,Human_Splice_Rec_747885,Human_Splice_Rec_747897,Human_Splice_Rec_747903,Human_Splice_Rec_747917,Human_Splice_Rec_747925,Human_Splice_Rec_747935 68909 RMVar_ID_68909 Human_SNP_ID_271574980 m1A Human chr6 + 29943460 29943460 29943460 GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCAGTTGAGAGCCTACCTGGATGGCACGTGCGTGG GCGCAAGTGGGAGGCGGCCCATGAGGCGGAGCTGTTGAGAGCCTACCTGGATGGCACGTGCGTGG A T HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:29943188..29943475 26863196 MeRIP-seq:(Medium) rs78674188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4878426,Human_RBP_ID_22405186,Human_RBP_ID_22773331 Human_Splice_Rec_747843,Human_Splice_Rec_747857,Human_Splice_Rec_747871,Human_Splice_Rec_747885,Human_Splice_Rec_747897,Human_Splice_Rec_747903,Human_Splice_Rec_747917,Human_Splice_Rec_747925,Human_Splice_Rec_747935 68910 RMVar_ID_68910 Human_SNP_ID_271575078 m1A Human chr6 + 29943517 29943517 29943517 GTGCGTGGAGTGGCTCCGCAGATACCTGGAGAACGGGAAGGAGACGCTGCAGCGCACGGGTACCA GTGCGTGGAGTGGCTCCGCAGATACCTGGAGAGCGGGAAGGAGACGCTGCAGCGCACGGGTACCA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29943227..29944175 26863196 MeRIP-seq:(Medium) rs281864759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22461006,Human_RBP_ID_22773332 Human_Splice_Rec_747843,Human_Splice_Rec_747857,Human_Splice_Rec_747871,Human_Splice_Rec_747885,Human_Splice_Rec_747897,Human_Splice_Rec_747903,Human_Splice_Rec_747917,Human_Splice_Rec_747925,Human_Splice_Rec_747935 68911 RMVar_ID_68911 Human_SNP_ID_271575088 m1A Human chr6 + 29943522 29943522 29943522 TGGAGTGGCTCCGCAGATACCTGGAGAACGGGAAGGAGACGCTGCAGCGCACGGGTACCAGGGGC TGGAGTGGCTCCGCAGATACCTGGAGAACGGGTAGGAGACGCTGCAGCGCACGGGTACCAGGGGC A T HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29943230..29943591 26863196 MeRIP-seq:(Medium) rs1270378288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22461006,Human_RBP_ID_22773332 Human_Splice_Rec_747843,Human_Splice_Rec_747857,Human_Splice_Rec_747871,Human_Splice_Rec_747885,Human_Splice_Rec_747897,Human_Splice_Rec_747903,Human_Splice_Rec_747917,Human_Splice_Rec_747925,Human_Splice_Rec_747935 68912 RMVar_ID_68912 Human_SNP_ID_271575378 m1A Human chr6 - 29944103 29944102 29944103 TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGAAAATTCAGGCATTTTGCATCTGTCATGGGACAC TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGATCATTCAGGCATTTTGCATCTGTCATGGGACAC TT GA HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr6:29944101..29944175 26863196,32194978 MeRIP-seq:(Medium) rs796376944 Functional Loss MNV dbSNP153 33..34 33 - - - 68913 RMVar_ID_68913 Human_SNP_ID_271575379 m1A Human chr6 - 29944103 29944103 29944103 TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGAAAATTCAGGCATTTTGCATCTGTCATGGGACAC TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGATAATTCAGGCATTTTGCATCTGTCATGGGACAC T A HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr6:29944101..29944175 26863196,32194978 MeRIP-seq:(Medium) rs17885212 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 68914 RMVar_ID_68914 Human_SNP_ID_271575577 m1A Human chr6 + 29944376 29944376 29944376 ACACCTGCCATGTGCAGCATGAGGGTCTGCCCAAGCCCCTCACCCTGAGATGGGGTAAGGAGGGA ACACCTGCCATGTGCAGCATGAGGGTCTGCCCGAGCCCCTCACCCTGAGATGGGGTAAGGAGGGA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29944326..29944375 26863196 MeRIP-seq:(Medium) rs1136835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18085724,Human_RBP_ID_22773335 Human_Splice_Rec_747845,Human_Splice_Rec_747859,Human_Splice_Rec_747873,Human_Splice_Rec_747887,Human_Splice_Rec_747899,Human_Splice_Rec_747905,Human_Splice_Rec_747919,Human_Splice_Rec_747927,Human_Splice_Rec_747937 Human_miRNA_ID_191307,Human_miRNA_ID_829992,Human_miRNA_ID_1235579,Human_miRNA_ID_1561887 68915 RMVar_ID_68915 Human_SNP_ID_271575720 m1A Human chr6 - 29944596 29944596 29944596 CCCCTTCTCCACCTGAGCTCTTCCTCCTCCACATCACGGCAGCGACCACAGCTCCAGTGATCACA CCCCTTCTCCACCTGAGCTCTTCCTCCTCCACCTCACGGCAGCGACCACAGCTCCAGTGATCACA T G HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29944547..29944653 26863196 MeRIP-seq:(Medium) rs1137110 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 68916 RMVar_ID_68916 Human_SNP_ID_271575727 m1A Human chr6 + 29944615 29944615 29944615 GTCGCTGCCGTGATGTGGAGGAGGAAGAGCTCAGGTGGAGAAGGGGTGAAGGGTGGGGTCTGAGA GTCGCTGCCGTGATGTGGAGGAGGAAGAGCTCTGGTGGAGAAGGGGTGAAGGGTGGGGTCTGAGA A T HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:29944566..29944658 26863196 MeRIP-seq:(Medium) rs1335784803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4878436,Human_RBP_ID_18072750 Human_Splice_Rec_747847,Human_Splice_Rec_747861,Human_Splice_Rec_747875,Human_Splice_Rec_747907,Human_Splice_Rec_747929,Human_Splice_Rec_747939 68917 RMVar_ID_68917 Human_SNP_ID_271576119 m1A Human chr6 + 29945521 29945521 29945521 GTTGTTCCTGCCCTTCCCTTTGTGACTTGAAGAACCCTGACTTTGTTTCTGCAAAGGCACCTGCA GTTGTTCCTGCCCTTCCCTTTGTGACTTGAAGTACCCTGACTTTGTTTCTGCAAAGGCACCTGCA A T HLA-A Ensembl:ENSG00000206503 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29945426..29945710 26863196 MeRIP-seq:(Medium) rs1061235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660487,Human_RBP_ID_1113066,Human_RBP_ID_1670035,Human_RBP_ID_2017697,Human_RBP_ID_3002121,Human_RBP_ID_3805444,Human_RBP_ID_4878448,Human_RBP_ID_8641269,Human_RBP_ID_17663567,Human_RBP_ID_21221562,Human_RBP_ID_22405188,Human_RBP_ID_22461010,Human_RBP_ID_24155770,Human_RBP_ID_24512090,Human_RBP_ID_26534959,Human_RBP_ID_27094924 Human_Splice_Rec_747852,Human_Splice_Rec_747866,Human_Splice_Rec_747880,Human_Splice_Rec_747892,Human_Splice_Rec_747900,Human_Splice_Rec_747912 Human_miRNA_ID_728016 Clinvar_Rec_278,Clinvar_Rec_2415 GWAS_ID_8232,GWAS_ID_8233,GWAS_ID_8234 68918 RMVar_ID_68918 Human_SNP_ID_271585427 m1A Human chr6 - 29976684 29976684 29976684 CCAGCGCAGCCGCGTCCTGAGTTACACACGCGACCACGCTGGGCCTTTTCTCTTTCTTTTCCGGA CCAGCGCAGCCGCGTCCTGAGTTACACACGCGCCCACGCTGGGCCTTTTCTCTTTCTTTTCCGGA T G HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:29976682..29976749 26863196 MeRIP-seq:(Medium) rs1330658642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18072768 68919 RMVar_ID_68919 Human_SNP_ID_271590434 m1A Human chr6 - 29993377 29993377 29993377 AATGAAGAAGTGAAGTGTGAAAAGATACAGAAAATAAGTGGGTGGGAGAGTGGGTGTCCCTCTGT AATGAAGAAGTGAAGTGTGAAAAGATACAGAACATAAGTGGGTGGGAGAGTGGGTGTCCCTCTGT T G HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS0000D5CB7C lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:29993374..29993454 26863196 MeRIP-seq:(Medium) rs1182202954 Functional Loss SNV dbSNP153 33..33 33 - - - 68920 RMVar_ID_68920 Human_SNP_ID_410138639 m1A Human chr9 + 105244574 105244574 105244574 GGGACTGGGCGCGGGAGGCGGGAGGCGGGGGGACAGAGGGAGGCGCCGCCGCCGCCGCCGCCCGC GGGACTGGGCGCGGGAGGCGGGAGGCGGGGGGGCAGAGGGAGGCGCCGCCGCCGCCGCCGCCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:105244487..105244772 26863196 MeRIP-seq:(Medium) rs1355691033 Functional Loss SNV dbSNP153 33..33 33 - - - 68921 RMVar_ID_68921 Human_SNP_ID_410138703 m1A Human chr9 + 105244704 105244704 105244704 GCCGCCGGGGGATGTGGCCGGCGCCTGCCTCTAGCCGCGCCGCCTCTTGAGTACCAGCCGCCGCT GCCGCCGGGGGATGTGGCCGGCGCCTGCCTCTGGCCGCGCCGCCTCTTGAGTACCAGCCGCCGCT A G SLC44A1 Ensembl:ENSG00000070214 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:105244479..105244735 26863196 MeRIP-seq:(Medium) rs1186179845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035787 RMVar_hsa_circ_116673,RMVar_hsa_circ_258396 68922 RMVar_ID_68922 Human_SNP_ID_410154019 m1A Human chr9 + 105309820 105309820 105309820 GCTATGGAAATATCTGTGGGCAGAAAAATACAAAGTTGGAAGCAATACCAAACAGTGGCATGGAC GCTATGGAAATATCTGTGGGCAGAAAAATACACAGTTGGAAGCAATACCAAACAGTGGCATGGAC A C SLC44A1 Ensembl:ENSG00000070214 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:105309770..105335617 32194978 MeRIP-seq:(Medium) rs368046201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9231168 Human_Splice_Rec_1068766,Human_Splice_Rec_1068767,Human_Splice_Rec_1068796,Human_Splice_Rec_1068797,Human_Splice_Rec_1068826,Human_Splice_Rec_1068827,Human_Splice_Rec_1068856,Human_Splice_Rec_1068857,Human_Splice_Rec_1068888,Human_Splice_Rec_1068889 Human_miRNA_ID_270430,Human_miRNA_ID_1317538,Human_miRNA_ID_2049398 RMVar_hsa_circ_34693,RMVar_hsa_circ_116673,RMVar_hsa_circ_314832,RMVar_hsa_circ_258397,RMVar_hsa_circ_258396,RMVar_hsa_circ_258398,RMVar_hsa_circ_341236,RMVar_hsa_circ_277799,RMVar_hsa_circ_305302,RMVar_hsa_circ_63831,RMVar_hsa_circ_52035,RMVar_hsa_circ_258399,RMVar_hsa_circ_258400,RMVar_hsa_circ_56354,RMVar_hsa_circ_307395,RMVar_hsa_circ_258401 68923 RMVar_ID_68923 Human_SNP_ID_410154020 m1A Human chr9 + 105309820 105309820 105309820 GCTATGGAAATATCTGTGGGCAGAAAAATACAAAGTTGGAAGCAATACCAAACAGTGGCATGGAC GCTATGGAAATATCTGTGGGCAGAAAAATACAGAGTTGGAAGCAATACCAAACAGTGGCATGGAC A G SLC44A1 Ensembl:ENSG00000070214 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:105309770..105335617 32194978 MeRIP-seq:(Medium) rs368046201 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9231168 Human_Splice_Rec_1068766,Human_Splice_Rec_1068767,Human_Splice_Rec_1068796,Human_Splice_Rec_1068797,Human_Splice_Rec_1068826,Human_Splice_Rec_1068827,Human_Splice_Rec_1068856,Human_Splice_Rec_1068857,Human_Splice_Rec_1068888,Human_Splice_Rec_1068889 Human_miRNA_ID_270430,Human_miRNA_ID_1317538,Human_miRNA_ID_2049398 RMVar_hsa_circ_34693,RMVar_hsa_circ_116673,RMVar_hsa_circ_314832,RMVar_hsa_circ_258397,RMVar_hsa_circ_258396,RMVar_hsa_circ_258398,RMVar_hsa_circ_341236,RMVar_hsa_circ_277799,RMVar_hsa_circ_305302,RMVar_hsa_circ_63831,RMVar_hsa_circ_52035,RMVar_hsa_circ_258399,RMVar_hsa_circ_258400,RMVar_hsa_circ_56354,RMVar_hsa_circ_307395,RMVar_hsa_circ_258401 68924 RMVar_ID_68924 Human_SNP_ID_410186815 m1A Human chr9 - 105448091 105448091 105448091 TGCCCCAGCCCGCACCGGCACCGCCCGGCCCCACCCGTCCGCGCCCAGACCGCGCGCGCCGTAGT TGCCCCAGCCCGCACCGGCACCGCCCGGCCCCGCCCGTCCGCGCCCAGACCGCGCGCGCCGTAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:105448052..105448191;chr9:105448043..105448219 26863196 MeRIP-seq:(Medium) rs910534624 Functional Loss SNV dbSNP153 33..33 33 - - - 68925 RMVar_ID_68925 Human_SNP_ID_410205228 m1A Human chr9 + 105519870 105519870 105519870 GAGCGGCGGCGGCAGGCGGCCAGCCCGGGTCTACCTCGCTCCGTGCAGGGCCGGGAGAGGGATCC GAGCGGCGGCGGCAGGCGGCCAGCCCGGGTCTGCCTCGCTCCGTGCAGGGCCGGGAGAGGGATCC A G FSD1L Ensembl:ENSG00000106701 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:105519766..105519918 26863196 MeRIP-seq:(Medium) rs1257923790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255781,Human_RBP_ID_847685,Human_RBP_ID_5036949,Human_RBP_ID_9407151 RMVar_hsa_circ_460,RMVar_hsa_circ_354339,RMVar_hsa_circ_44343,RMVar_hsa_circ_320081,RMVar_hsa_circ_265682,RMVar_hsa_circ_275004,RMVar_hsa_circ_35118,RMVar_hsa_circ_258436,RMVar_hsa_circ_287991,RMVar_hsa_circ_258438,RMVar_hsa_circ_58664 68926 RMVar_ID_68926 Human_SNP_ID_410214245 m1A Human chr9 + 105558184 105558184 105558184 TGCTGTTGAGTGAGGTAAGGTACGGGAGGCTCAGGTCGGTACCCGGGGATGGGTGGGCGCCTTCA TGCTGTTGAGTGAGGTAAGGTACGGGAGGCTCTGGTCGGTACCCGGGGATGGGTGGGCGCCTTCA A T FKTN Ensembl:ENSG00000106692 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:105558170..105558317 26863196 MeRIP-seq:(Medium) rs943139460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19145414 68927 RMVar_ID_68927 Human_SNP_ID_410233416 m1A Human chr9 - 105635531 105635531 105635531 GGGTGGGGGAGGGTTCCCTCAAAGGAAAATTGAGTTGTTTACCAAAAGGAGGAATAAAAGAAGTA GGGTGGGGGAGGGTTCCCTCAAAGGAAAATTGGGTTGTTTACCAAAAGGAGGAATAAAAGAAGTA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:105635426..105635558 26863196 MeRIP-seq:(Medium) rs188381546 Functional Loss SNV dbSNP153 33..33 33 - - - 68928 RMVar_ID_68928 Human_SNP_ID_410249978 m1A Human chr9 + 105705647 105705647 105705647 GGAAGAATCCTATTTCAAGCTGGTTTACTGCTATGCTCCACTGTTTTGGTGGAGGAATTTTATCC GGAAGAATCCTATTTCAAGCTGGTTTACTGCTGTGCTCCACTGTTTTGGTGGAGGAATTTTATCC A G TMEM38B Ensembl:ENSG00000095209 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:105705555..105705648 32194978 MeRIP-seq:(Medium) rs140337245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_708287,Human_RBP_ID_5036954,Human_RBP_ID_8693670,Human_RBP_ID_18901671,Human_RBP_ID_24277466 Human_Splice_Rec_1069304,Human_Splice_Rec_1069316,Human_Splice_Rec_1069318 RMVar_hsa_circ_258450,RMVar_hsa_circ_290873,RMVar_hsa_circ_311026,RMVar_hsa_circ_107384,RMVar_hsa_circ_273045,RMVar_hsa_circ_258452,RMVar_hsa_circ_258453,RMVar_hsa_circ_258451 68929 RMVar_ID_68929 Human_SNP_ID_410540118 m1A Human chr9 - 106862420 106862420 106862420 GCGTGCGCGCTCGCGTCCCGGTGGCGCCCGGCAGCCCTGGCCCGCAGAGGAAGCCCCCGGTGAGG GCGTGCGCGCTCGCGTCCCGGTGGCGCCCGGCCGCCCTGGCCCGCAGAGGAAGCCCCCGGTGAGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:106862324..106862495 26863196 MeRIP-seq:(Medium) rs1376495052 Functional Loss SNV dbSNP153 33..33 33 - - - 68930 RMVar_ID_68930 Human_SNP_ID_410540405 m1A Human chr9 + 106863157 106863157 106863157 AGGGAGAGAGACGGATATCTCAGGTCATCTGCAGCTGCAGCGAGTCTGAGGAGCCGAGGAAGGCA AGGGAGAGAGACGGATATCTCAGGTCATCTGCTGCTGCAGCGAGTCTGAGGAGCCGAGGAAGGCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:106863014..106863301 26863196 MeRIP-seq:(Medium) rs1173345070 Functional Loss SNV dbSNP153 33..33 33 - - - 68931 RMVar_ID_68931 Human_SNP_ID_410540426 m1A Human chr9 + 106863233 106863233 106863233 GATCCTCCATTGCTGAGACCCGGCAGAAGCACATGAGACTCCCAAACAACTTCCACAACAATAAC GATCCTCCATTGCTGAGACCCGGCAGAAGCACTTGAGACTCCCAAACAACTTCCACAACAATAAC A T ZNF462 Ensembl:ENSG00000148143 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:106863182..106863290 26863196 MeRIP-seq:(Medium) rs1221998044 Functional Loss SNV dbSNP153 33..33 33 - - - 68932 RMVar_ID_68932 Human_SNP_ID_410540941 m1A Human chr9 - 106864162 106864162 106864162 TGTTCACCAGCAGCACCGGCACCAGCAGCTGCAGCAGCCACCCCCCGACACATCCCGACCCCGCA TGTTCACCAGCAGCACCGGCACCAGCAGCTGCTGCAGCCACCCCCCGACACATCCCGACCCCGCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:106864149..106864304 26863196 MeRIP-seq:(Medium) rs1167391576 Functional Loss SNV dbSNP153 33..33 33 - - - 68933 RMVar_ID_68933 Human_SNP_ID_410542624 m1A Human chr9 - 106871393 106871393 106871393 CCAGTCACTCCTTCCCAGCAAATTTCCACTATAAAATTACAGCAATGCTTTAGCCTACTTTCCTG CCAGTCACTCCTTCCCAGCAAATTTCCACTATGAAATTACAGCAATGCTTTAGCCTACTTTCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:106871391..106871473 26863196 MeRIP-seq:(Medium) rs1564067896 Functional Loss SNV dbSNP153 33..33 33 - - - 68934 RMVar_ID_68934 Human_SNP_ID_410555404 m1A Human chr9 + 106925553 106925535 106925553 TTGCAGCAGCAACAGCCACCGCAGCCACCACCACCGCCGCCGCCACCACCACCATCACAGCCACA TTGCAGCAGCAACAG__________________CCGCCGCCGCCACCACCACCATCACAGCCACA GCCACCGCAGCCACCACCA G ZNF462 Ensembl:ENSG00000148143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:106925505..106925720 26863196 MeRIP-seq:(Medium) rs753867598 Functional Loss DEL dbSNP153 16..33 33 - - - RMVar_hsa_circ_32088,RMVar_hsa_circ_270134,RMVar_hsa_circ_303314,RMVar_hsa_circ_337158,RMVar_hsa_circ_62543,RMVar_hsa_circ_258461,RMVar_hsa_circ_258462 68935 RMVar_ID_68935 Human_SNP_ID_410555420 m1A Human chr9 + 106925553 106925553 106925553 TTGCAGCAGCAACAGCCACCGCAGCCACCACCACCGCCGCCGCCACCACCACCATCACAGCCACA TTGCAGCAGCAACAGCCACCGCAGCCACCACCGCCGCCGCCGCCACCACCACCATCACAGCCACA A G ZNF462 Ensembl:ENSG00000148143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:106925505..106925720 26863196 MeRIP-seq:(Medium) rs146183570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32088,RMVar_hsa_circ_270134,RMVar_hsa_circ_303314,RMVar_hsa_circ_337158,RMVar_hsa_circ_62543,RMVar_hsa_circ_258461,RMVar_hsa_circ_258462 68936 RMVar_ID_68936 Human_SNP_ID_410641817 m1A Human chr9 - 107283462 107283462 107283462 TCACATTCGCCCAGCGGAGCGGCCTCTCCCCCAGCCCGTGCCCCGGACCGCGCCGCTGCCTCCGC TCACATTCGCCCAGCGGAGCGGCCTCTCCCCCCGCCCGTGCCCCGGACCGCGCCGCTGCCTCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:107283251..107283700;chr9:107283251..107283733 26863196 MeRIP-seq:(Medium) rs1208291386 Functional Loss SNV dbSNP153 33..33 33 - - - 68937 RMVar_ID_68937 Human_SNP_ID_410641837 m1A Human chr9 + 107283533 107283533 107283533 CCCACCCCCACCGCCTTCCTCCCCAGAGCGCGAGGAGCGCGGGCGACCCCGGGGCCCCGCCAGGC CCCACCCCCACCGCCTTCCTCCCCAGAGCGCGGGGAGCGCGGGCGACCCCGGGGCCCCGCCAGGC A G RAD23B Ensembl:ENSG00000119318 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:107283276..107283681 26863196 MeRIP-seq:(Medium) rs1470756183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5005047,Human_RBP_ID_26360402,Human_RBP_ID_26834122 Human_Splice_Rec_1069722 RMVar_hsa_circ_86606,RMVar_hsa_circ_258469,RMVar_hsa_circ_82835,RMVar_hsa_circ_258468 68938 RMVar_ID_68938 Human_SNP_ID_410646424 m1A Human chr9 - 107300084 107300084 107300084 TTGGAAAAAGTCTAAATAAAAAATGACAATCCAGAATCTGAATAAATAATGGAAGACAAAAATTA TTGGAAAAAGTCTAAATAAAAAATGACAATCCTGAATCTGAATAAATAATGGAAGACAAAAATTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:107300081..107300160 26863196 MeRIP-seq:(Medium) rs577764641 Functional Loss SNV dbSNP153 33..33 33 - - - 68939 RMVar_ID_68939 Human_SNP_ID_410646425 m1A Human chr9 - 107300084 107300084 107300084 TTGGAAAAAGTCTAAATAAAAAATGACAATCCAGAATCTGAATAAATAATGGAAGACAAAAATTA TTGGAAAAAGTCTAAATAAAAAATGACAATCCGGAATCTGAATAAATAATGGAAGACAAAAATTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:107300081..107300160 26863196 MeRIP-seq:(Medium) rs577764641 Functional Loss SNV dbSNP153 33..33 33 - - - 68940 RMVar_ID_68940 Human_SNP_ID_410646451 m1A Human chr9 + 107300149 107300149 107300149 AACAAATCTTTATTTTTCCTATAGGTGAAAGCACTGAAAGAGAAGATTGAATCTGAAAAGGGGAA AACAAATCTTTATTTTTCCTATAGGTGAAAGCGCTGAAAGAGAAGATTGAATCTGAAAAGGGGAA A G RAD23B Ensembl:ENSG00000119318 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:107300126..107300150 26863196 MeRIP-seq:(Medium) rs1250534573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90679,Human_RBP_ID_965229,Human_RBP_ID_1700850,Human_RBP_ID_5038042,Human_RBP_ID_5226230,Human_RBP_ID_16532821,Human_RBP_ID_24277931 Human_Splice_Rec_1069724,Human_Splice_Rec_1069725,Human_Splice_Rec_1069730,Human_Splice_Rec_1069731,Human_Splice_Rec_1069748,Human_Splice_Rec_1069749,Human_Splice_Rec_1069766,Human_Splice_Rec_1069767 RMVar_hsa_circ_94036,RMVar_hsa_circ_86606,RMVar_hsa_circ_116427,RMVar_hsa_circ_258469,RMVar_hsa_circ_82835,RMVar_hsa_circ_258468,RMVar_hsa_circ_258470,RMVar_hsa_circ_258473,RMVar_hsa_circ_285053,RMVar_hsa_circ_305134,RMVar_hsa_circ_258471,RMVar_hsa_circ_305695,RMVar_hsa_circ_285417,RMVar_hsa_circ_122814,RMVar_hsa_circ_272227,RMVar_hsa_circ_258475,RMVar_hsa_circ_258476,RMVar_hsa_circ_258474,RMVar_hsa_circ_258472 68941 RMVar_ID_68941 Human_SNP_ID_410648331 m1A Human chr9 + 107306484 107306484 107306484 CCTCCACCACCACAACTGTGGCTCAGGCTCCAACCCCTGTCCCTGCCTTGGCCCCCACTTCCACA CCTCCACCACCACAACTGTGGCTCAGGCTCCAGCCCCTGTCCCTGCCTTGGCCCCCACTTCCACA A G RAD23B Ensembl:ENSG00000119318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:107306436..107306516 26863196 MeRIP-seq:(Medium) rs1207439891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90681,Human_RBP_ID_708412,Human_RBP_ID_5005060,Human_RBP_ID_7885450,Human_RBP_ID_17094894,Human_RBP_ID_17323583,Human_RBP_ID_17437123,Human_RBP_ID_17550696,Human_RBP_ID_18127118,Human_RBP_ID_26559687,Human_RBP_ID_27368940 RMVar_hsa_circ_94036,RMVar_hsa_circ_86606,RMVar_hsa_circ_116427,RMVar_hsa_circ_258469,RMVar_hsa_circ_82835,RMVar_hsa_circ_258468,RMVar_hsa_circ_258470,RMVar_hsa_circ_258473,RMVar_hsa_circ_285053,RMVar_hsa_circ_305134,RMVar_hsa_circ_258471,RMVar_hsa_circ_285417,RMVar_hsa_circ_122814,RMVar_hsa_circ_272227,RMVar_hsa_circ_258475,RMVar_hsa_circ_258476,RMVar_hsa_circ_258474,RMVar_hsa_circ_258478,RMVar_hsa_circ_258480,RMVar_hsa_circ_294780,RMVar_hsa_circ_344919,RMVar_hsa_circ_258472,RMVar_hsa_circ_324083,RMVar_hsa_circ_270702,RMVar_hsa_circ_258479,RMVar_hsa_circ_258482,RMVar_hsa_circ_296150,RMVar_hsa_circ_310086,RMVar_hsa_circ_258477,RMVar_hsa_circ_302527,RMVar_hsa_circ_258483,RMVar_hsa_circ_258481 68942 RMVar_ID_68942 Human_SNP_ID_410648348 m1A Human chr9 + 107306508 107306508 107306508 AGGCTCCAACCCCTGTCCCTGCCTTGGCCCCCACTTCCACACCTGCATCCATCACTCCAGCATCA AGGCTCCAACCCCTGTCCCTGCCTTGGCCCCCGCTTCCACACCTGCATCCATCACTCCAGCATCA A G RAD23B Ensembl:ENSG00000119318 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:107306457..107306563 26863196 MeRIP-seq:(Medium) rs1434356414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90681,Human_RBP_ID_708412,Human_RBP_ID_7885451,Human_RBP_ID_17094894,Human_RBP_ID_17320664,Human_RBP_ID_17434996,Human_RBP_ID_17547711,Human_RBP_ID_18127118,Human_RBP_ID_18901815,Human_RBP_ID_27368940 RMVar_hsa_circ_94036,RMVar_hsa_circ_86606,RMVar_hsa_circ_116427,RMVar_hsa_circ_258469,RMVar_hsa_circ_82835,RMVar_hsa_circ_258468,RMVar_hsa_circ_258470,RMVar_hsa_circ_258473,RMVar_hsa_circ_285053,RMVar_hsa_circ_305134,RMVar_hsa_circ_258471,RMVar_hsa_circ_285417,RMVar_hsa_circ_122814,RMVar_hsa_circ_272227,RMVar_hsa_circ_258475,RMVar_hsa_circ_258476,RMVar_hsa_circ_258474,RMVar_hsa_circ_258478,RMVar_hsa_circ_258480,RMVar_hsa_circ_294780,RMVar_hsa_circ_344919,RMVar_hsa_circ_258472,RMVar_hsa_circ_324083,RMVar_hsa_circ_270702,RMVar_hsa_circ_258479,RMVar_hsa_circ_258482,RMVar_hsa_circ_296150,RMVar_hsa_circ_310086,RMVar_hsa_circ_258477,RMVar_hsa_circ_302527,RMVar_hsa_circ_258483,RMVar_hsa_circ_258481 68943 RMVar_ID_68943 Human_SNP_ID_410653252 m1A Human chr9 + 107324887 107324887 107324887 CATTTTATTCAGATGTTAAATGAACCAGTTCAAGAAGCTGGTGGTCAAGGAGGAGGAGGTGGAGG CATTTTATTCAGATGTTAAATGAACCAGTTCAGGAAGCTGGTGGTCAAGGAGGAGGAGGTGGAGG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs753505436 Functional Loss SNV dbSNP153 33..33 33 - - - 68944 RMVar_ID_68944 Human_SNP_ID_410653269 m1A Human chr9 - 107324926 107324926 107324926 ATATGACCACTTCCAGCTTCTGCAATTCCTCCACTGCCACCTCCACCTCCTCCTCCTTGACCACC ATATGACCACTTCCAGCTTCTGCAATTCCTCCGCTGCCACCTCCACCTCCTCCTCCTTGACCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:107324877..107324952 26863196 MeRIP-seq:(Medium) rs1306351995 Functional Loss SNV dbSNP153 33..33 33 - - - 68945 RMVar_ID_68945 Human_SNP_ID_410695675 m1A Human chr9 - 107487649 107487649 107487649 CTGGCAGCGAGTACGGCAGCCCGTCGGTCATCAGCGTCAGCAAAGGCAGCCCTGACGGCAGCCAC CTGGCAGCGAGTACGGCAGCCCGTCGGTCATCGGCGTCAGCAAAGGCAGCCCTGACGGCAGCCAC T C KLF4 Ensembl:ENSG00000136826 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:107487598..107487746 26863196 MeRIP-seq:(Medium) rs746813034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27128775 68946 RMVar_ID_68946 Human_SNP_ID_410695798 m1A Human chr9 - 107487867 107487867 107487867 CGGCACGGGCGGAGGCCTCCTCTATGGCAGGGAGTCCGCTCCCCCTCCGACGGCTCCCTTCAACC CGGCACGGGCGGAGGCCTCCTCTATGGCAGGGGGTCCGCTCCCCCTCCGACGGCTCCCTTCAACC T C KLF4 Ensembl:ENSG00000136826 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:107487816..107488191 26863196 MeRIP-seq:(Medium) rs780704509 Functional Loss SNV dbSNP153 33..33 33 - - - 68947 RMVar_ID_68947 Human_SNP_ID_410696584 m1A Human chr9 - 107489522 107489522 107489522 CCGCGCCACGGCAGCCAGTCTCACCTGGCGGCACCGCCCGCCCACCGCCCCGGCCACAGCCCCTG CCGCGCCACGGCAGCCAGTCTCACCTGGCGGCGCCGCCCGCCCACCGCCCCGGCCACAGCCCCTG T C KLF4 Ensembl:ENSG00000136826 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:107489351..107489650 26863196 MeRIP-seq:(Medium) rs1254547721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1069848 68948 RMVar_ID_68948 Human_SNP_ID_410696587 m1A Human chr9 - 107489547 107489547 107489547 TTGCGCCGCCGACCAGTTCGCAGCTCCGCGCCACGGCAGCCAGTCTCACCTGGCGGCACCGCCCG TTGCGCCGCCGACCAGTTCGCAGCTCCGCGCCGCGGCAGCCAGTCTCACCTGGCGGCACCGCCCG T C KLF4 Ensembl:ENSG00000136826 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:107489465..107489727 26863410 MeRIP-seq:(Medium) rs1401779728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5005154 Human_Splice_Rec_1069848 68949 RMVar_ID_68949 Human_SNP_ID_410696680 m1A Human chr9 + 107489738 107489738 107489738 CGCCACCGCCTCTGCTCCCCGCGCGCCCGCAGACACGTTCGTTCTCTCTGGTCGGGAAACTGCCG CGCCACCGCCTCTGCTCCCCGCGCGCCCGCAGGCACGTTCGTTCTCTCTGGTCGGGAAACTGCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:107489436..107489748;chr9:107489703..107489822;chr9:107489687..107489823 26863196 MeRIP-seq:(Medium) rs899453088 Functional Loss SNV dbSNP153 33..33 33 - - - 68950 RMVar_ID_68950 Human_SNP_ID_411076840 m1A Human chr9 - 108933963 108933963 108933963 GAGCCGCGGACAGAGACGCGTGCGCAATTCGGAGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC GAGCCGCGGACAGAGACGCGTGCGCAATTCGGTGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC T A ELP1 Ensembl:ENSG00000070061 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:108933913..108934036 26863196 MeRIP-seq:(Medium) rs117100816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255744,Human_RBP_ID_5005295,Human_RBP_ID_9315604,Human_RBP_ID_16535203,Human_RBP_ID_23094622,Human_RBP_ID_23120897 Human_Splice_Rec_1069877,Human_Splice_Rec_1069949 Clinvar_Rec_279,Clinvar_Rec_280 RMVar_hsa_circ_103885,RMVar_hsa_circ_258504 68951 RMVar_ID_68951 Human_SNP_ID_411076841 m1A Human chr9 - 108933963 108933963 108933963 GAGCCGCGGACAGAGACGCGTGCGCAATTCGGAGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC GAGCCGCGGACAGAGACGCGTGCGCAATTCGGGGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC T C ELP1 Ensembl:ENSG00000070061 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:108933913..108934036 26863196 MeRIP-seq:(Medium) rs117100816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255744,Human_RBP_ID_5005295,Human_RBP_ID_9315604,Human_RBP_ID_16535203,Human_RBP_ID_23094622,Human_RBP_ID_23120897 Human_Splice_Rec_1069877,Human_Splice_Rec_1069949 Clinvar_Rec_279,Clinvar_Rec_280 RMVar_hsa_circ_103885,RMVar_hsa_circ_258504 68952 RMVar_ID_68952 Human_SNP_ID_411076842 m1A Human chr9 - 108933963 108933963 108933963 GAGCCGCGGACAGAGACGCGTGCGCAATTCGGAGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC GAGCCGCGGACAGAGACGCGTGCGCAATTCGGCGCCGACTCTGGGTGCGGACTGTGGGAGCTGAC T G ELP1 Ensembl:ENSG00000070061 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:108933913..108934036 26863196 MeRIP-seq:(Medium) rs117100816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255744,Human_RBP_ID_5005295,Human_RBP_ID_9315604,Human_RBP_ID_16535203,Human_RBP_ID_23094622,Human_RBP_ID_23120897 Human_Splice_Rec_1069877,Human_Splice_Rec_1069949 Clinvar_Rec_279,Clinvar_Rec_280 RMVar_hsa_circ_103885,RMVar_hsa_circ_258504 68953 RMVar_ID_68953 Human_SNP_ID_411077174 m1A Human chr9 + 108934504 108934504 108934504 GCGCCGGAGGTCGCCATGGCTACCGAGCCCGAAGCCGCGGAGCCGGTGGTGCCTTCGCTCGTGGA GCGCCGGAGGTCGCCATGGCTACCGAGCCCGAGGCCGCGGAGCCGGTGGTGCCTTCGCTCGTGGA A G ABITRAM Ensembl:ENSG00000119328 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:108934460..108935647;chr9:108934457..108934532 26863196 MeRIP-seq:(Medium) rs765297645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_708604,Human_RBP_ID_5036308,Human_RBP_ID_8944634,Human_RBP_ID_9338998 Human_Splice_Rec_1070017,Human_Splice_Rec_1070027,Human_Splice_Rec_1070029,Human_Splice_Rec_1070035 68954 RMVar_ID_68954 Human_SNP_ID_411077198 m1A Human chr9 - 108934544 108934544 108934544 TCCGCACTTACCCGGTTTGTACCAGCGAGTGAAGTATCGATCCACGAGCGAAGGCACCACCGGCT TCCGCACTTACCCGGTTTGTACCAGCGAGTGAGGTATCGATCCACGAGCGAAGGCACCACCGGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:108934451..108934575 26863410 MeRIP-seq:(Medium) rs1167353907 Functional Loss SNV dbSNP153 33..33 33 - - - 68955 RMVar_ID_68955 Human_SNP_ID_411083185 m1A Human chr9 - 108960342 108960342 108960342 GTGATCTATCCAGAGAAGAGACGATGGTCTATACTAGGGTGATGATAGTCAAGATGAAGATAAGG GTGATCTATCCAGAGAAGAGACGATGGTCTATGCTAGGGTGATGATAGTCAAGATGAAGATAAGG T C CTNNAL1 Ensembl:ENSG00000119326 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:108960337..108960402 26863196 MeRIP-seq:(Medium) rs1372836957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68341,RMVar_hsa_circ_342574,RMVar_hsa_circ_22498,RMVar_hsa_circ_258510 68956 RMVar_ID_68956 Human_SNP_ID_411095186 m1A Human chr9 - 109013425 109013396 109013425 GATAGACCGAGGGCCATGGCCGCCTCTCCCGGACCCGCCGGCGTTGGCGGCGCCGGAGCAGTCTA GATAGACCGAGGGCCATGGCCGCCTCTCCCGG_____________________________TCTA ACTGCTCCGGCGCCGCCAACGCCGGCGGGT A CTNNAL1 Ensembl:ENSG00000119326 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:109013326..109013529 26863410 MeRIP-seq:(Medium) rs768941003 Functional Loss DEL dbSNP153 33..61 33 - - - Human_RBP_ID_5035797,Human_RBP_ID_8930133,Human_RBP_ID_9315151,Human_RBP_ID_9339524,Human_RBP_ID_17437129,Human_RBP_ID_22466949 68957 RMVar_ID_68957 Human_SNP_ID_411095190 m1A Human chr9 - 109013401 109013401 109013401 TCTCCCGGACCCGCCGGCGTTGGCGGCGCCGGAGCAGTCTACGGCTCCGGCTCTTCGGGCTTCGC TCTCCCGGACCCGCCGGCGTTGGCGGCGCCGGGGCAGTCTACGGCTCCGGCTCTTCGGGCTTCGC T C CTNNAL1 Ensembl:ENSG00000119326 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109013361..109013500 26863196 MeRIP-seq:(Medium) rs1055615393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_708657,Human_RBP_ID_5035797,Human_RBP_ID_8930133,Human_RBP_ID_9315151,Human_RBP_ID_9339524 Human_Splice_Rec_1070043,Human_Splice_Rec_1070079,Human_Splice_Rec_1070131 68958 RMVar_ID_68958 Human_SNP_ID_411095208 m1A Human chr9 - 109013425 109013425 109013425 GATAGACCGAGGGCCATGGCCGCCTCTCCCGGACCCGCCGGCGTTGGCGGCGCCGGAGCAGTCTA GATAGACCGAGGGCCATGGCCGCCTCTCCCGGCCCCGCCGGCGTTGGCGGCGCCGGAGCAGTCTA T G CTNNAL1 Ensembl:ENSG00000119326 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:109013326..109013529 26863410 MeRIP-seq:(Medium) rs1193623339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035797,Human_RBP_ID_8930133,Human_RBP_ID_9315151,Human_RBP_ID_9339524,Human_RBP_ID_17437129,Human_RBP_ID_22466949 68959 RMVar_ID_68959 Human_SNP_ID_411100100 m1A Human chr9 - 109033480 109033480 109033480 CTTTATTCCAGAGGTGGCCATCCTTACCTGACAGGCTTGGCAGTGGCCGGTGGAGCATACTACCT CTTTATTCCAGAGGTGGCCATCCTTACCTGACGGGCTTGGCAGTGGCCGGTGGAGCATACTACCT T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:109033351..109033525 32194978 MeRIP-seq:(Medium) rs1000574595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9231487,Human_RBP_ID_17323460,Human_RBP_ID_17550744,Human_RBP_ID_19024053,Human_RBP_ID_22776892 Human_Splice_Rec_1070168,Human_Splice_Rec_1070174,Human_Splice_Rec_1070196,Human_Splice_Rec_1070226 Human_miRNA_ID_2225247 RMVar_hsa_circ_258522,RMVar_hsa_circ_276708,RMVar_hsa_circ_329834,RMVar_hsa_circ_375073,RMVar_hsa_circ_116226,RMVar_hsa_circ_258512,RMVar_hsa_circ_376282,RMVar_hsa_circ_360177,RMVar_hsa_circ_373686,RMVar_hsa_circ_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_272966,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,RMVar_hsa_circ_258524,RMVar_hsa_circ_258525,RMVar_hsa_circ_258523,RMVar_hsa_circ_258514,RMVar_hsa_circ_258518,RMVar_hsa_circ_258520,RMVar_hsa_circ_258521,RMVar_hsa_circ_258519,RMVar_hsa_circ_258516,RMVar_hsa_circ_258517,RMVar_hsa_circ_258515,RMVar_hsa_circ_258513 68960 RMVar_ID_68960 Human_SNP_ID_411107809 m1A Human chr9 - 109063767 109063767 109063767 GAGACAGGAGTGTGCTTGAAGAGATGATTGAGATGCTGAGACAGGAGTGTGCTTGAGGAAATGAT GAGACAGGAGTGTGCTTGAAGAGATGATTGAGTTGCTGAGACAGGAGTGTGCTTGAGGAAATGAT T A TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:109063722..109063841 26863196 MeRIP-seq:(Medium) rs117010877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16536693,Human_RBP_ID_24278521 RMVar_hsa_circ_258553,RMVar_hsa_circ_26606,RMVar_hsa_circ_329834,RMVar_hsa_circ_375073,RMVar_hsa_circ_116226,RMVar_hsa_circ_258512,RMVar_hsa_circ_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_258514,RMVar_hsa_circ_258518,RMVar_hsa_circ_258516,RMVar_hsa_circ_258517,RMVar_hsa_circ_258515,RMVar_hsa_circ_310854,RMVar_hsa_circ_258513,RMVar_hsa_circ_335640,RMVar_hsa_circ_107760,RMVar_hsa_circ_269198,RMVar_hsa_circ_102086,RMVar_hsa_circ_116087,RMVar_hsa_circ_258526,RMVar_hsa_circ_258528,RMVar_hsa_circ_258529,RMVar_hsa_circ_258527,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_122294,RMVar_hsa_circ_258541,RMVar_hsa_circ_280270,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258531,RMVar_hsa_circ_294617,RMVar_hsa_circ_300656,RMVar_hsa_circ_374311,RMVar_hsa_circ_351398,RMVar_hsa_circ_283020,RMVar_hsa_circ_87627,RMVar_hsa_circ_277318,RMVar_hsa_circ_258543,RMVar_hsa_circ_258544,RMVar_hsa_circ_258542,RMVar_hsa_circ_258537,RMVar_hsa_circ_258539,RMVar_hsa_circ_258540,RMVar_hsa_circ_258538,RMVar_hsa_circ_126174,RMVar_hsa_circ_258536,RMVar_hsa_circ_125084,RMVar_hsa_circ_92631,RMVar_hsa_circ_115756,RMVar_hsa_circ_93834,RMVar_hsa_circ_60247,RMVar_hsa_circ_83182,RMVar_hsa_circ_258554,RMVar_hsa_circ_12019,RMVar_hsa_circ_258563,RMVar_hsa_circ_258549,RMVar_hsa_circ_258551,RMVar_hsa_circ_258552,RMVar_hsa_circ_258550,RMVar_hsa_circ_290458,RMVar_hsa_circ_320156,RMVar_hsa_circ_353260,RMVar_hsa_circ_258548,RMVar_hsa_circ_373949,RMVar_hsa_circ_322933,RMVar_hsa_circ_275145,RMVar_hsa_circ_288270,RMVar_hsa_circ_258559,RMVar_hsa_circ_258561,RMVar_hsa_circ_258562,RMVar_hsa_circ_258560,RMVar_hsa_circ_69704,RMVar_hsa_circ_338665,RMVar_hsa_circ_258558,RMVar_hsa_circ_278031,RMVar_hsa_circ_31879,RMVar_hsa_circ_729 68961 RMVar_ID_68961 Human_SNP_ID_411122189 m1A Human chr9 - 109119567 109119567 109119567 CCGCCACTGGCTGCAGCGCCTGCACCGCGCGCACACGCCCATCGTCCTGGCCGCGCTGCTCCTGC CCGCCACTGGCTGCAGCGCCTGCACCGCGCGCGCACGCCCATCGTCCTGGCCGCGCTGCTCCTGC T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109119496..109119691 26863196 MeRIP-seq:(Medium) rs982587248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255793,Human_RBP_ID_5036965,Human_RBP_ID_17437134,Human_RBP_ID_27540971 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584 68962 RMVar_ID_68962 Human_SNP_ID_411122230 m1A Human chr9 + 109119625 109119625 109119625 GTGGCGGCCCAGGCGCGTCAGCGAGCTCTTGAAGGGGTGCAGAAAAGTGCCGCATAGCACGGCCC GTGGCGGCCCAGGCGCGTCAGCGAGCTCTTGAGGGGGTGCAGAAAAGTGCCGCATAGCACGGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:109119576..109119664 26863196 MeRIP-seq:(Medium) rs1394154014 Functional Loss SNV dbSNP153 33..33 33 - - - 68963 RMVar_ID_68963 Human_SNP_ID_411122231 m1A Human chr9 + 109119625 109119625 109119625 GTGGCGGCCCAGGCGCGTCAGCGAGCTCTTGAAGGGGTGCAGAAAAGTGCCGCATAGCACGGCCC GTGGCGGCCCAGGCGCGTCAGCGAGCTCTTGATGGGGTGCAGAAAAGTGCCGCATAGCACGGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:109119576..109119664 26863196 MeRIP-seq:(Medium) rs1394154014 Functional Loss SNV dbSNP153 33..33 33 - - - 68964 RMVar_ID_68964 Human_SNP_ID_411122347 m1A Human chr9 - 109119799 109119799 109119799 GGCCGAGTGGCGGTGGCGGGGAGACCCCGCGGACCGCGGCGCTGGCGCTGCGCTTCGACAAGCCC GGCCGAGTGGCGGTGGCGGGGAGACCCCGCGGGCCGCGGCGCTGGCGCTGCGCTTCGACAAGCCC T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:109119751..109119925;chr9:109119751..109119950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_797151,Human_RBP_ID_5005548,Human_RBP_ID_8930616,Human_RBP_ID_9339527,Human_RBP_ID_22466444 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584,RMVar_hsa_circ_266828 68965 RMVar_ID_68965 Human_SNP_ID_411122353 m1A Human chr9 - 109119808 109119808 109119808 GCGCGGTCGGGCCGAGTGGCGGTGGCGGGGAGACCCCGCGGACCGCGGCGCTGGCGCTGCGCTTC GCGCGGTCGGGCCGAGTGGCGGTGGCGGGGAGTCCCCGCGGACCGCGGCGCTGGCGCTGCGCTTC T A TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:109119766..109119901 26863196 MeRIP-seq:(Medium) rs1298020750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035805,Human_RBP_ID_8930616,Human_RBP_ID_9339527,Human_RBP_ID_22466444 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584 68966 RMVar_ID_68966 Human_SNP_ID_411122430 m1A Human chr9 - 109119892 109119892 109119892 GCGGAGGAACGATGGCCGACGGCGGCGGCCCTAAGGACGCGCCAAGCCTGCGGAGCTCTCCCGGG GCGGAGGAACGATGGCCGACGGCGGCGGCCCTGAGGACGCGCCAAGCCTGCGGAGCTCTCCCGGG T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr9:109119701..109119950;chr9:109119751..109119950;chr9:109119802..109119898 26863196,26863410 MeRIP-seq:(Medium) rs528527374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797152,Human_RBP_ID_5005550,Human_RBP_ID_18427196,Human_RBP_ID_22466951 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584 68967 RMVar_ID_68967 Human_SNP_ID_411171964 m1A Human chr9 + 109320221 109320218 109320221 GTAGAGGGTGGCCTTGGCGGCGCCGGCGGCGGAGATGTGCACGGCCGCGCCGCCGGTGAGCAGGG GTAGAGGGTGGCCTTGGCGGCGCCGGCGGC___GATGTGCACGGCCGCGCCGCCGGTGAGCAGGG CGGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:109320171..109320277 26863196 MeRIP-seq:(Medium) rs1350774674 Functional Loss DEL dbSNP153 31..33 33 - - - 68968 RMVar_ID_68968 Human_SNP_ID_411171968 m1A Human chr9 + 109320221 109320221 109320221 GTAGAGGGTGGCCTTGGCGGCGCCGGCGGCGGAGATGTGCACGGCCGCGCCGCCGGTGAGCAGGG GTAGAGGGTGGCCTTGGCGGCGCCGGCGGCGGCGATGTGCACGGCCGCGCCGCCGGTGAGCAGGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:109320171..109320277 26863196 MeRIP-seq:(Medium) rs763606162 Functional Loss SNV dbSNP153 33..33 33 - - - 68969 RMVar_ID_68969 Human_SNP_ID_411171971 m1A Human chr9 + 109320229 109320229 109320229 TGGCCTTGGCGGCGCCGGCGGCGGAGATGTGCACGGCCGCGCCGCCGGTGAGCAGGGGCCCGCCG TGGCCTTGGCGGCGCCGGCGGCGGAGATGTGCTCGGCCGCGCCGCCGGTGAGCAGGGGCCCGCCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109320192..109320359 26863196 MeRIP-seq:(Medium) rs1283815397 Functional Loss SNV dbSNP153 33..33 33 - - - 68970 RMVar_ID_68970 Human_SNP_ID_411172303 m1A Human chr9 - 109321035 109321008 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGC___________________________TGGAGG AGCCGCCGCCGCCGCCGCCGCCGCCGCT A RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs1008526216 Functional Loss DEL dbSNP153 33..59 33 - - - 68971 RMVar_ID_68971 Human_SNP_ID_411172325 m1A Human chr9 - 109321035 109321020 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGC_______________GGCGGCGGCGGCTGGAGG CGCCGCCGCCGCCGCT C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs1427017471 Functional Loss DEL dbSNP153 33..47 33 - - - 68972 RMVar_ID_68972 Human_SNP_ID_411172330 m1A Human chr9 - 109321035 109321023 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGC____________GGCGGCGGCGGCGGCTGGAGG CGCCGCCGCCGCT C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs571464370 Functional Loss DEL dbSNP153 33..44 33 - - - 68973 RMVar_ID_68973 Human_SNP_ID_411172334 m1A Human chr9 - 109321035 109321026 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGC_________GGCGGCGGCGGCGGCGGCTGGAGG CGCCGCCGCT C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs1203525570 Functional Loss DEL dbSNP153 33..41 33 - - - 68974 RMVar_ID_68974 Human_SNP_ID_411172337 m1A Human chr9 - 109321035 109321032 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGC___GGCGGCGGCGGCGGCGGCGGCGGCTGGAGG CGCT C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs919063403 Functional Loss DEL dbSNP153 33..35 33 - - - 68975 RMVar_ID_68975 Human_SNP_ID_411172343 m1A Human chr9 - 109321035 109321035 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCTGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG T A RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs1467993034 Functional Loss SNV dbSNP153 33..33 33 - - - 68976 RMVar_ID_68976 Human_SNP_ID_411172344 m1A Human chr9 - 109321035 109321035 109321035 GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG GAGGGAGGAGGGCGTGCTGCAGTCCCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGGAGG T C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109279896..109321068 26863196 MeRIP-seq:(Medium) rs1467993034 Functional Loss SNV dbSNP153 33..33 33 - - - 68977 RMVar_ID_68977 Human_SNP_ID_411189087 m1A Human chr9 + 109389313 109389310 109389313 CTGATCCCAGACAACCTGCCAAAACTGTGCACAGGTATGCGGCAGGGGCCCCTGAGTGGCGATGT CTGATCCCAGACAACCTGCCAAAACTGTGC___GGTATGCGGCAGGGGCCCCTGAGTGGCGATGT CACA C HSALNG0073606 RNACentral:URS0000EBD502 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:109389172..109389312 26863196 MeRIP-seq:(Medium) rs764717487 Functional Loss DEL dbSNP153 31..33 33 - - - 68978 RMVar_ID_68978 Human_SNP_ID_411284495 m1A Human chr9 + 109780333 109780333 109780333 AGGCTGAGCCCGGGCGAGCCCGCCGTGCGCACAGCTCTGCCCGCCGCCCCTGGAGCGGATCCCCA AGGCTGAGCCCGGGCGAGCCCGCCGTGCGCACGGCTCTGCCCGCCGCCCCTGGAGCGGATCCCCA A G PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:109780203..109780415 26863196 MeRIP-seq:(Medium) rs554058303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5005633 Clinvar_Rec_281 68979 RMVar_ID_68979 Human_SNP_ID_411291563 m1A Human chr9 + 109810652 109810652 109810652 CTTCAAGGAGTTTTGCTGTAAAGAGGAATAGAAAATGGAGTAGTAGATGAGGGAGATTGTGGGCT CTTCAAGGAGTTTTGCTGTAAAGAGGAATAGACAATGGAGTAGTAGATGAGGGAGATTGTGGGCT A C PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109810644..109810873 26863196 MeRIP-seq:(Medium) rs1379910773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_321422 68980 RMVar_ID_68980 Human_SNP_ID_411299435 m1A Human chr9 - 109841959 109841959 109841959 TCTATCCCTCCAACTTCCCCTCCATCCCCCTCACCCTCCCCTCTTTCCTTCCACCCTCCCCTCTA TCTATCCCTCCAACTTCCCCTCCATCCCCCTCGCCCTCCCCTCTTTCCTTCCACCCTCCCCTCTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109841944..109842202 26863196 MeRIP-seq:(Medium) rs1001558083 Functional Loss SNV dbSNP153 33..33 33 - - - 68981 RMVar_ID_68981 Human_SNP_ID_411299436 m1A Human chr9 - 109841959 109841959 109841959 TCTATCCCTCCAACTTCCCCTCCATCCCCCTCACCCTCCCCTCTTTCCTTCCACCCTCCCCTCTA TCTATCCCTCCAACTTCCCCTCCATCCCCCTCCCCCTCCCCTCTTTCCTTCCACCCTCCCCTCTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109841944..109842202 26863196 MeRIP-seq:(Medium) rs1001558083 Functional Loss SNV dbSNP153 33..33 33 - - - 68982 RMVar_ID_68982 Human_SNP_ID_411317189 m1A Human chr9 + 109917117 109917117 109917117 AAATGTGGAAGAGGGAGGCAGAAATCAGAAGGAGGGGTGGCTGCAGGGAAGGTCAGAGAGATGCA AAATGTGGAAGAGGGAGGCAGAAATCAGAAGGTGGGGTGGCTGCAGGGAAGGTCAGAGAGATGCA A T PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109917107..109917250 26863196 MeRIP-seq:(Medium) rs1403990169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356952,RMVar_hsa_circ_258611,RMVar_hsa_circ_307523 68983 RMVar_ID_68983 Human_SNP_ID_411333834 m1A Human chr9 + 109988667 109988663 109988668 GGAAGGAGGAAGGAAGGAAAAGAAGGGAAGGAAGGGAAGGGAAGGGAAAGGAAGGGCGGGAGGAG GGAAGGAGGAAGGAAGGAAAAGAAGGGAA_____GGAAGGGAAGGGAAAGGAAGGGCGGGAGGAG AGGAAG A PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109988661..109988744 26863196 MeRIP-seq:(Medium) rs1489089916 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_72021,RMVar_hsa_circ_357590 68984 RMVar_ID_68984 Human_SNP_ID_411359937 m1A Human chr9 + 110093314 110093314 110093314 GGATGTGAGATGTAATATTTTGGGAGGAAAATAGTGGAAATTGAGTGACTGCGGGACTCGGCTAA GGATGTGAGATGTAATATTTTGGGAGGAAAATCGTGGAAATTGAGTGACTGCGGGACTCGGCTAA A C PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:110093309..110093382 26863196 MeRIP-seq:(Medium) rs1019171348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24278869 RMVar_hsa_circ_69313,RMVar_hsa_circ_258613,RMVar_hsa_circ_82318 68985 RMVar_ID_68985 Human_SNP_ID_411370301 m1A Human chr9 + 110136861 110136861 110136861 GAGCATGAGAAAGAACAATACTGCATTAGAAAAGTGAGGCCTTCAGAGGAGATGCTGGAGCTGGA GAGCATGAGAAAGAACAATACTGCATTAGAAAGGTGAGGCCTTCAGAGGAGATGCTGGAGCTGGA A G PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:110136812..110137023 26863196 MeRIP-seq:(Medium) rs546782241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69313,RMVar_hsa_circ_258614,RMVar_hsa_circ_258613,RMVar_hsa_circ_82318,RMVar_hsa_circ_287280,RMVar_hsa_circ_347540,RMVar_hsa_circ_258615 68986 RMVar_ID_68986 Human_SNP_ID_411370396 m1A Human chr9 - 110137076 110137076 110137076 GCTGCTGCTGCTGCTGCTGTAACTGCTTCTGCAGCAGCAACTGTTCCTGCTGTGCCCTTCTCTCT GCTGCTGCTGCTGCTGCTGTAACTGCTTCTGCTGCAGCAACTGTTCCTGCTGTGCCCTTCTCTCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:110137026..110137126 32194978 MeRIP-seq:(Medium) rs1297414133 Functional Loss SNV dbSNP153 33..33 33 - - - 68987 RMVar_ID_68987 Human_SNP_ID_411377988 m1A Human chr9 + 110168879 110168879 110168879 GACAATGGTGGTAGGGCCACTTAGAGAGCAGTAGGGCCCAGGCTGGTGCAGCCTACATGGCACAG GACAATGGTGGTAGGGCCACTTAGAGAGCAGTGGGGCCCAGGCTGGTGCAGCCTACATGGCACAG A G PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:110168829..110168930 32194978 MeRIP-seq:(Medium) rs1394242545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22411091 68988 RMVar_ID_68988 Human_SNP_ID_411378154 m1A Human chr9 - 110169650 110169650 110169650 CTTTGTATCATCCTGAAACACACTGGTTGCTCAGCAAAAATAGTATCTCTTACCTCCTTATTTTA CTTTGTATCATCCTGAAACACACTGGTTGCTCGGCAAAAATAGTATCTCTTACCTCCTTATTTTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:110169603..110169709 26863196 MeRIP-seq:(Medium) rs961794301 Functional Loss SNV dbSNP153 33..33 33 - - - 68989 RMVar_ID_68989 Human_SNP_ID_411397444 m1A Human chr9 - 110244188 110244188 110244188 GGTGGGTGAATTTTCTGGAGCCAATAAGGAAAAGCTTGAAGCCACCATTAATGAATTAGTCTAAT GGTGGGTGAATTTTCTGGAGCCAATAAGGAAACGCTTGAAGCCACCATTAATGAATTAGTCTAAT T G TXN Ensembl:ENSG00000136810 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:110244051..110244865 32194978 MeRIP-seq:(Medium) rs776464764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_708919,Human_RBP_ID_3890838,Human_RBP_ID_9231607,Human_RBP_ID_17666753,Human_RBP_ID_22466952,Human_RBP_ID_24278945,Human_RBP_ID_26559901 Human_Splice_Rec_1070694,Human_Splice_Rec_1070700,Human_Splice_Rec_1070702 68990 RMVar_ID_68990 Human_SNP_ID_411400985 m1A Human chr9 + 110256467 110256467 110256467 TCTTGGCTGCTGGAGTCTGACGAGCGGCTGTAAGGACCGATGGAAATGGATCCAAAGCACCAAAC TCTTGGCTGCTGGAGTCTGACGAGCGGCTGTAGGGACCGATGGAAATGGATCCAAAGCACCAAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:110245112..110256575 32194978 MeRIP-seq:(Medium) rs1369067214 Functional Loss SNV dbSNP153 33..33 33 - - - 68991 RMVar_ID_68991 Human_SNP_ID_411400999 m1A Human chr9 - 110256481 110256481 110256481 AGTCTTGAAGCTCTGTTTGGTGCTTTGGATCCATTTCCATCGGTCCTTACAGCCGCTCGTCAGAC AGTCTTGAAGCTCTGTTTGGTGCTTTGGATCCGTTTCCATCGGTCCTTACAGCCGCTCGTCAGAC T C TXN Ensembl:ENSG00000136810 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:110256110..110256600 26863196 MeRIP-seq:(Medium) rs776271419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15761,Human_RBP_ID_708933,Human_RBP_ID_1057479,Human_RBP_ID_1225662,Human_RBP_ID_1337416,Human_RBP_ID_1402182,Human_RBP_ID_1701050,Human_RBP_ID_2059324,Human_RBP_ID_5005768,Human_RBP_ID_5329582,Human_RBP_ID_5431450,Human_RBP_ID_5454812,Human_RBP_ID_5482491,Human_RBP_ID_5515480,Human_RBP_ID_8694347,Human_RBP_ID_9231611,Human_RBP_ID_9339003,Human_RBP_ID_16538937,Human_RBP_ID_18902094,Human_RBP_ID_21669890,Human_RBP_ID_22334344,Human_RBP_ID_22467374,Human_RBP_ID_24278996,Human_RBP_ID_27128877,Human_RBP_ID_27369139 Human_Splice_Rec_1070687,Human_Splice_Rec_1070695 68992 RMVar_ID_68992 Human_SNP_ID_411401000 m1A Human chr9 + 110256490 110256481 110256490 GCGGCTGTAAGGACCGATGGAAATGGATCCAAAGCACCAAACAGAGCTTCAAGACTCGCTGCTTG GCGGCTGTAAGGACCGATGGAAAT_________GCACCAAACAGAGCTTCAAGACTCGCTGCTTG TGGATCCAAA T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:110251442..110256640 26863410 MeRIP-seq:(Medium) rs1564082083 Functional Loss DEL dbSNP153 25..33 33 - - - 68993 RMVar_ID_68993 Human_SNP_ID_411690420 m1A Human chr9 + 111422200 111422200 111422200 GCTATATCCTTAGTGAATAAATGTGGCATCCGACTGCAAAAGAATGTAAAAATATTGTTACTATC GCTATATCCTTAGTGAATAAATGTGGCATCCGTCTGCAAAAGAATGTAAAAATATTGTTACTATC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111422171..111425438 32194978 MeRIP-seq:(Medium) rs374393215 Functional Loss SNV dbSNP153 33..33 33 - - - 68994 RMVar_ID_68994 Human_SNP_ID_411695445 m1A Human chr9 - 111442337 111442337 111442337 AATGTGAACTGGCCCCTACGCTTCTTACTGCCATGGAAGGGAAGCCTCAGCCACAGCAGGATAGG AATGTGAACTGGCCCCTACGCTTCTTACTGCCGTGGAAGGGAAGCCTCAGCCACAGCAGGATAGG T C ECPAS Ensembl:ENSG00000136813 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111440515..111442400 32194978 MeRIP-seq:(Medium) rs889665904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26833396 Human_Splice_Rec_1071160,Human_Splice_Rec_1071161,Human_Splice_Rec_1071260,Human_Splice_Rec_1071261,Human_Splice_Rec_1071368,Human_Splice_Rec_1071369,Human_Splice_Rec_1071414 RMVar_hsa_circ_10083,RMVar_hsa_circ_84724,RMVar_hsa_circ_71534,RMVar_hsa_circ_258665,RMVar_hsa_circ_123255,RMVar_hsa_circ_258672,RMVar_hsa_circ_80828,RMVar_hsa_circ_258673,RMVar_hsa_circ_115679,RMVar_hsa_circ_258677,RMVar_hsa_circ_70693,RMVar_hsa_circ_26656,RMVar_hsa_circ_105654,RMVar_hsa_circ_258687,RMVar_hsa_circ_100196,RMVar_hsa_circ_258689,RMVar_hsa_circ_119338,RMVar_hsa_circ_258697,RMVar_hsa_circ_315592,RMVar_hsa_circ_332686,RMVar_hsa_circ_50558,RMVar_hsa_circ_306684,RMVar_hsa_circ_64760,RMVar_hsa_circ_71757,RMVar_hsa_circ_258704,RMVar_hsa_circ_80294,RMVar_hsa_circ_258707,RMVar_hsa_circ_311495,RMVar_hsa_circ_276468,RMVar_hsa_circ_104769,RMVar_hsa_circ_10507,RMVar_hsa_circ_258713,RMVar_hsa_circ_258714,RMVar_hsa_circ_258715,RMVar_hsa_circ_2592,RMVar_hsa_circ_336258,RMVar_hsa_circ_272135,RMVar_hsa_circ_258719,RMVar_hsa_circ_284079,RMVar_hsa_circ_282304,RMVar_hsa_circ_258718,RMVar_hsa_circ_258723,RMVar_hsa_circ_111318,RMVar_hsa_circ_286196,RMVar_hsa_circ_272359,RMVar_hsa_circ_258724,RMVar_hsa_circ_258722,RMVar_hsa_circ_333280,RMVar_hsa_circ_258726,RMVar_hsa_circ_268992,RMVar_hsa_circ_275610,RMVar_hsa_circ_282025,RMVar_hsa_circ_273266,RMVar_hsa_circ_258727,RMVar_hsa_circ_258729,RMVar_hsa_circ_258725,RMVar_hsa_circ_334332,RMVar_hsa_circ_258728 68995 RMVar_ID_68995 Human_SNP_ID_411695446 m1A Human chr9 - 111442337 111442337 111442337 AATGTGAACTGGCCCCTACGCTTCTTACTGCCATGGAAGGGAAGCCTCAGCCACAGCAGGATAGG AATGTGAACTGGCCCCTACGCTTCTTACTGCCCTGGAAGGGAAGCCTCAGCCACAGCAGGATAGG T G ECPAS Ensembl:ENSG00000136813 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111440515..111442400 32194978 MeRIP-seq:(Medium) rs889665904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26833396 Human_Splice_Rec_1071160,Human_Splice_Rec_1071161,Human_Splice_Rec_1071260,Human_Splice_Rec_1071261,Human_Splice_Rec_1071368,Human_Splice_Rec_1071369,Human_Splice_Rec_1071414 RMVar_hsa_circ_10083,RMVar_hsa_circ_84724,RMVar_hsa_circ_71534,RMVar_hsa_circ_258665,RMVar_hsa_circ_123255,RMVar_hsa_circ_258672,RMVar_hsa_circ_80828,RMVar_hsa_circ_258673,RMVar_hsa_circ_115679,RMVar_hsa_circ_258677,RMVar_hsa_circ_70693,RMVar_hsa_circ_26656,RMVar_hsa_circ_105654,RMVar_hsa_circ_258687,RMVar_hsa_circ_100196,RMVar_hsa_circ_258689,RMVar_hsa_circ_119338,RMVar_hsa_circ_258697,RMVar_hsa_circ_315592,RMVar_hsa_circ_332686,RMVar_hsa_circ_50558,RMVar_hsa_circ_306684,RMVar_hsa_circ_64760,RMVar_hsa_circ_71757,RMVar_hsa_circ_258704,RMVar_hsa_circ_80294,RMVar_hsa_circ_258707,RMVar_hsa_circ_311495,RMVar_hsa_circ_276468,RMVar_hsa_circ_104769,RMVar_hsa_circ_10507,RMVar_hsa_circ_258713,RMVar_hsa_circ_258714,RMVar_hsa_circ_258715,RMVar_hsa_circ_2592,RMVar_hsa_circ_336258,RMVar_hsa_circ_272135,RMVar_hsa_circ_258719,RMVar_hsa_circ_284079,RMVar_hsa_circ_282304,RMVar_hsa_circ_258718,RMVar_hsa_circ_258723,RMVar_hsa_circ_111318,RMVar_hsa_circ_286196,RMVar_hsa_circ_272359,RMVar_hsa_circ_258724,RMVar_hsa_circ_258722,RMVar_hsa_circ_333280,RMVar_hsa_circ_258726,RMVar_hsa_circ_268992,RMVar_hsa_circ_275610,RMVar_hsa_circ_282025,RMVar_hsa_circ_273266,RMVar_hsa_circ_258727,RMVar_hsa_circ_258729,RMVar_hsa_circ_258725,RMVar_hsa_circ_334332,RMVar_hsa_circ_258728 68996 RMVar_ID_68996 Human_SNP_ID_411703659 m1A Human chr9 - 111474309 111474309 111474309 GGAGTTAGAGATGAATCTAAATCTGACCTGAGACTAGAAGGTGGAGGAGTAACAGAGAGTGTAGC GGAGTTAGAGATGAATCTAAATCTGACCTGAGGCTAGAAGGTGGAGGAGTAACAGAGAGTGTAGC T C ECPAS Ensembl:ENSG00000136813 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:111474307..111474442 26863196 MeRIP-seq:(Medium) rs1251582829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84724,RMVar_hsa_circ_258665,RMVar_hsa_circ_105654,RMVar_hsa_circ_258687,RMVar_hsa_circ_80294,RMVar_hsa_circ_258707,RMVar_hsa_circ_104769,RMVar_hsa_circ_258714 68997 RMVar_ID_68997 Human_SNP_ID_411706075 m1A Human chr9 + 111483359 111483359 111483359 AGCGGCGACGGTCCGCGCCCCGCCCGTCCGCCAGGCCCGGGCTCCCCAGCTCCCCGTACGCCGCG AGCGGCGACGGTCCGCGCCCCGCCCGTCCGCCGGGCCCGGGCTCCCCAGCTCCCCGTACGCCGCG A G RF00017-4932,RF00017-1190 RNACentral:URS000096C9DE,RNACentral:URS000092EF5C SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:111483355..111483420 26863196 MeRIP-seq:(Medium) rs1045330096 Functional Loss SNV dbSNP153 33..33 33 - - - 68998 RMVar_ID_68998 Human_SNP_ID_411706294 m1A Human chr9 - 111483804 111483804 111483804 CGGGCCTGGCGCACGGGGATTCGGCCGCACAGACGGCGGCGGCGGCAGCGGCAGCGGCTCCGCAG CGGGCCTGGCGCACGGGGATTCGGCCGCACAGGCGGCGGCGGCGGCAGCGGCAGCGGCTCCGCAG T C ECPAS Ensembl:ENSG00000136813 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:111483754..111483853 26863196 MeRIP-seq:(Medium) rs1186113561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036320,Human_RBP_ID_24443476 RMVar_hsa_circ_84724,RMVar_hsa_circ_258665,RMVar_hsa_circ_105654,RMVar_hsa_circ_258687,RMVar_hsa_circ_80294,RMVar_hsa_circ_258707,RMVar_hsa_circ_104769,RMVar_hsa_circ_258714 68999 RMVar_ID_68999 Human_SNP_ID_411706508 m1A Human chr9 + 111484211 111484196 111484211 GAGCGAGGCGTTCGGCGGGCCGGGCCCCGGGGAGCCGCGCGCCGCAGTCCGTGAGGGGCTGGGCC GAGCGAGGCGTTCGGCGG_______________GCCGCGCGCCGCAGTCCGTGAGGGGCTGGGCC GGCCGGGCCCCGGGGA G RF00017-4932,RF00017-1190 RNACentral:URS000096C9DE,RNACentral:URS000092EF5C SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:111484162..111484321 26863196 MeRIP-seq:(Medium) rs779426592 Functional Loss DEL dbSNP153 19..33 33 - - - 69000 RMVar_ID_69000 Human_SNP_ID_411706520 m1A Human chr9 + 111484211 111484211 111484211 GAGCGAGGCGTTCGGCGGGCCGGGCCCCGGGGAGCCGCGCGCCGCAGTCCGTGAGGGGCTGGGCC GAGCGAGGCGTTCGGCGGGCCGGGCCCCGGGGGGCCGCGCGCCGCAGTCCGTGAGGGGCTGGGCC A G RF00017-4932,RF00017-1190 RNACentral:URS000096C9DE,RNACentral:URS000092EF5C SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:111484162..111484321 26863196 MeRIP-seq:(Medium) rs973238637 Functional Loss SNV dbSNP153 33..33 33 - - - 69001 RMVar_ID_69001 Human_SNP_ID_411706533 m1A Human chr9 - 111484230 111484230 111484230 GGGCAGCCCGGGCCCGCTCGGCCCAGCCCCTCACGGACTGCGGCGCGCGGCTCCCCGGGGCCCGG GGGCAGCCCGGGCCCGCTCGGCCCAGCCCCTCGCGGACTGCGGCGCGCGGCTCCCCGGGGCCCGG T C ECPAS Ensembl:ENSG00000136813 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:111484184..111484341 26863196 MeRIP-seq:(Medium) rs1162282778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255952,Human_RBP_ID_5006004,Human_RBP_ID_5482494,Human_RBP_ID_5515487,Human_RBP_ID_8930148,Human_RBP_ID_9339005 Human_Splice_Rec_1071254 RMVar_hsa_circ_84724,RMVar_hsa_circ_258665,RMVar_hsa_circ_105654,RMVar_hsa_circ_258687,RMVar_hsa_circ_80294,RMVar_hsa_circ_258707,RMVar_hsa_circ_104769,RMVar_hsa_circ_258714 69002 RMVar_ID_69002 Human_SNP_ID_411706562 m1A Human chr9 + 111484278 111484278 111484278 GCGGGCCCGGGCTGCCCTAGCGGCCGGGGGAAATCCTCGAGGCGGGGCCGGAGCGCCCTTTTCCG GCGGGCCCGGGCTGCCCTAGCGGCCGGGGGAAGTCCTCGAGGCGGGGCCGGAGCGCCCTTTTCCG A G RF00017-4932,RF00017-1190 RNACentral:URS000096C9DE,RNACentral:URS000092EF5C SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:111484176..111484350 26863410 MeRIP-seq:(Medium) rs1053977660 Functional Loss SNV dbSNP153 33..33 33 - - - 69003 RMVar_ID_69003 Human_SNP_ID_411706576 m1A Human chr9 + 111484297 111484297 111484297 GCGGCCGGGGGAAATCCTCGAGGCGGGGCCGGAGCGCCCTTTTCCGAGGTCTGCGGCTGTCACGT GCGGCCGGGGGAAATCCTCGAGGCGGGGCCGGGGCGCCCTTTTCCGAGGTCTGCGGCTGTCACGT A G RF00017-4932,RF00017-1190 RNACentral:URS000096C9DE,RNACentral:URS000092EF5C SRP RNA,SRP RNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:111484197..111484318 26863196 MeRIP-seq:(Medium) rs753140355 Functional Loss SNV dbSNP153 33..33 33 - - - 69004 RMVar_ID_69004 Human_SNP_ID_411725837 m1A Human chr9 - 111559133 111559130 111559134 GGATCCCAAGGAGGCTGAGGAGGTGCTGATGCATGGATAGCTTGGCAGGGAGGTCAGAGCCTGAG GGATCCCAAGGAGGCTGAGGAGGTGCTGATG____GATAGCTTGGCAGGGAGGTCAGAGCCTGAG CCATG C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:111559083..111559175 26863196 MeRIP-seq:(Medium) rs1312148697 Functional Loss DEL dbSNP153 32..35 33 - - - 69005 RMVar_ID_69005 Human_SNP_ID_411727241 m1A Human chr9 - 111563190 111563190 111563190 CAGTACAAGGAATATATCATTGAAGGATTTGAAAACATGCCAGCTGCATTTATGGGAATGCTGAA CAGTACAAGGAATATATCATTGAAGGATTTGAGAACATGCCAGCTGCATTTATGGGAATGCTGAA T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111563143..111563243 32194978 MeRIP-seq:(Medium) rs776584363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1071482,Human_Splice_Rec_1071502,Human_Splice_Rec_1071520 Human_miRNA_ID_207308,Human_miRNA_ID_1491034,Human_miRNA_ID_2012591,Human_miRNA_ID_2758967 RMVar_hsa_circ_100335,RMVar_hsa_circ_258738 69006 RMVar_ID_69006 Human_SNP_ID_411731951 m1A Human chr9 - 111583578 111583578 111583578 TCCTTAATTTTCTTCCTTTAGCCTGACTGCCTACTTTGGCCTACTTGAAATCTGTGGTGTGAAGG TCCTTAATTTTCTTCCTTTAGCCTGACTGCCTGCTTTGGCCTACTTGAAATCTGTGGTGTGAAGG T C PTGR1 Ensembl:ENSG00000106853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:111583527..111583624 26863196 MeRIP-seq:(Medium) rs557474998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1071456,Human_Splice_Rec_1071474,Human_Splice_Rec_1071492,Human_Splice_Rec_1071512,Human_Splice_Rec_1071530,Human_Splice_Rec_1071546 Human_miRNA_ID_1465277,Human_miRNA_ID_2009986,Human_miRNA_ID_2281723,Human_miRNA_ID_2283288,Human_miRNA_ID_2631338 RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_362175,RMVar_hsa_circ_352934,RMVar_hsa_circ_270545,RMVar_hsa_circ_347804,RMVar_hsa_circ_284418,RMVar_hsa_circ_258739,RMVar_hsa_circ_258740,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_295250,RMVar_hsa_circ_282441,RMVar_hsa_circ_351440,RMVar_hsa_circ_258741,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_350767,RMVar_hsa_circ_357371,RMVar_hsa_circ_258742,RMVar_hsa_circ_353363 69007 RMVar_ID_69007 Human_SNP_ID_411732582 m1A Human chr9 - 111586510 111586510 111586510 AGAGGAAAATCTCAACGATTCTGGAAAGTGGAAGGCTAAGGGAAAGAGAGCGACACCTGAAGAAG AGAGGAAAATCTCAACGATTCTGGAAAGTGGATGGCTAAGGGAAAGAGAGCGACACCTGAAGAAG T A PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:111586508..111586688 26863196 MeRIP-seq:(Medium) rs1408360951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_352934,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_295250,RMVar_hsa_circ_351440,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_364665,RMVar_hsa_circ_332381 69008 RMVar_ID_69008 Human_SNP_ID_411732768 m1A Human chr9 + 111587111 111587111 111587111 TGCTAGGATTACAGGTGTAAGCCACTGCGCCCAGCCTACCCTTTTCCACTCTATTAACACAGGGT TGCTAGGATTACAGGTGTAAGCCACTGCGCCCGGCCTACCCTTTTCCACTCTATTAACACAGGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:111587106..111587277 26863196 MeRIP-seq:(Medium) rs1464504958 Functional Loss SNV dbSNP153 33..33 33 - - - 69009 RMVar_ID_69009 Human_SNP_ID_411735407 m1A Human chr9 - 111597405 111597405 111597405 TCTAGGAGCTTCAGGATGGTTCGTACTAAGACATGGACCCTGAAGAAGCACTTTGTTGGCTATCC TCTAGGAGCTTCAGGATGGTTCGTACTAAGACGTGGACCCTGAAGAAGCACTTTGTTGGCTATCC T C PTGR1 Ensembl:ENSG00000106853 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111592919..111597407 32194978 MeRIP-seq:(Medium) rs1289683600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5006143 Human_Splice_Rec_1071448,Human_Splice_Rec_1071449,Human_Splice_Rec_1071466,Human_Splice_Rec_1071467,Human_Splice_Rec_1071484,Human_Splice_Rec_1071485,Human_Splice_Rec_1071504,Human_Splice_Rec_1071505,Human_Splice_Rec_1071521,Human_Splice_Rec_1071540,Human_Splice_Rec_1071541,Human_Splice_Rec_1071548,Human_Splice_Rec_1071549,Human_Splice_Rec_1071554,Human_Splice_Rec_1071555,Human_Splice_Rec_1071559 Human_miRNA_ID_1942408,Human_miRNA_ID_2116599,Human_miRNA_ID_2200173,Human_miRNA_ID_2203239,Human_miRNA_ID_2322011,Human_miRNA_ID_2325177,Human_miRNA_ID_2519554,Human_miRNA_ID_2835319,Human_miRNA_ID_3112691 RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_331329,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 69010 RMVar_ID_69010 Human_SNP_ID_411735850 m1A Human chr9 + 111599152 111599152 111599152 GGGCCAGGTCCCGGGAAAGTCTCGCCCGCCCGAGGAGGGGGCCTGGCGCGGCGCCCGGCCTTTGC GGGCCAGGTCCCGGGAAAGTCTCGCCCGCCCGTGGAGGGGGCCTGGCGCGGCGCCCGGCCTTTGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:111599143..111599375 26863196 MeRIP-seq:(Medium) rs1480182747 Functional Loss SNV dbSNP153 33..33 33 - - - 69011 RMVar_ID_69011 Human_SNP_ID_411744394 m1A Human chr9 + 111631395 111631395 111631395 TGCTGCAGAATCGCTGGGGTGGCAGAGCCGCCAGCGAGGCTGGGGATGGGGGCGCCGCTGCTCTC TGCTGCAGAATCGCTGGGGTGGCAGAGCCGCCGGCGAGGCTGGGGATGGGGGCGCCGCTGCTCTC A G DNAJC25-GNG10,DNAJC25 Ensembl:ENSG00000244115,Ensembl:ENSG00000059769 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:111631345..111631725;chr9:111631344..111642845 26863196 MeRIP-seq:(Medium) rs1022484564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256511,Human_RBP_ID_709002,Human_RBP_ID_846402,Human_RBP_ID_5035810,Human_RBP_ID_18427784 69012 RMVar_ID_69012 Human_SNP_ID_411744395 m1A Human chr9 + 111631395 111631395 111631395 TGCTGCAGAATCGCTGGGGTGGCAGAGCCGCCAGCGAGGCTGGGGATGGGGGCGCCGCTGCTCTC TGCTGCAGAATCGCTGGGGTGGCAGAGCCGCCTGCGAGGCTGGGGATGGGGGCGCCGCTGCTCTC A T DNAJC25-GNG10,DNAJC25 Ensembl:ENSG00000244115,Ensembl:ENSG00000059769 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:111631345..111631725;chr9:111631344..111642845 26863196 MeRIP-seq:(Medium) rs1022484564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256511,Human_RBP_ID_709002,Human_RBP_ID_846402,Human_RBP_ID_5035810,Human_RBP_ID_18427784 69013 RMVar_ID_69013 Human_SNP_ID_411780609 m1A Human chr9 + 111795202 111795202 111795202 AGGCTAGAAAGAGCTGGTTGTGAAGGGTTGGGAAGACCCGGCAAAGCAGTCCGGACTTCTTTGGG AGGCTAGAAAGAGCTGGTTGTGAAGGGTTGGGCAGACCCGGCAAAGCAGTCCGGACTTCTTTGGG A C HSALNG0073715 RNACentral:URS0000E9C683 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:111795044..111795408 26863196 MeRIP-seq:(Medium) rs1007267395 Functional Loss SNV dbSNP153 33..33 33 - - - 69014 RMVar_ID_69014 Human_SNP_ID_411804600 m1A Human chr9 + 111896852 111896840 111896852 CGGAGCTGCGGCGGTGGAGCTGCTCGGCCGGGAGCCCGGCGGCGAGACGGAGAGGCGGCGGAGGT CGGAGCTGCGGCGGTGGAGCT____________GCCCGGCGGCGAGACGGAGAGGCGGCGGAGGT TGCTCGGCCGGGA T UGCG Ensembl:ENSG00000148154 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:111896800..111897270 26863196 MeRIP-seq:(Medium) rs1309149829 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5006194,Human_RBP_ID_18427785,Human_RBP_ID_22467378 69015 RMVar_ID_69015 Human_SNP_ID_411804616 m1A Human chr9 + 111896870 111896870 111896870 GCTGCTCGGCCGGGAGCCCGGCGGCGAGACGGAGAGGCGGCGGAGGTGCCCGCGCGCAGGGTCTG GCTGCTCGGCCGGGAGCCCGGCGGCGAGACGGCGAGGCGGCGGAGGTGCCCGCGCGCAGGGTCTG A C UGCG Ensembl:ENSG00000148154 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:111896765..111897262 26863196 MeRIP-seq:(Medium) rs1054342017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256707,Human_RBP_ID_5035811,Human_RBP_ID_9339533,Human_RBP_ID_18427785,Human_RBP_ID_22466446 69016 RMVar_ID_69016 Human_SNP_ID_411804648 m1A Human chr9 + 111896946 111896946 111896946 CGAGGCTCGGGAGAGGCGAACCGGAGCGCGGGACCGCGGTCGCCCCGACCAGAGCCGGGAGACCG CGAGGCTCGGGAGAGGCGAACCGGAGCGCGGGCCCGCGGTCGCCCCGACCAGAGCCGGGAGACCG A C UGCG Ensembl:ENSG00000148154 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:111896846..111897025 26863410 MeRIP-seq:(Medium) rs7871397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036983,Human_RBP_ID_5154437,Human_RBP_ID_5329585,Human_RBP_ID_22118805,Human_RBP_ID_23094345,Human_RBP_ID_26361960 GWAS_ID_8235,GWAS_ID_8236,GWAS_ID_8237,GWAS_ID_8238,GWAS_ID_8239,GWAS_ID_8240,GWAS_ID_8241,GWAS_ID_8242,GWAS_ID_8243,GWAS_ID_8244,GWAS_ID_8245,GWAS_ID_8246,GWAS_ID_8247,GWAS_ID_8248,GWAS_ID_8249,GWAS_ID_8250,GWAS_ID_8251,GWAS_ID_8252,GWAS_ID_8253,GWAS_ID_8254,GWAS_ID_8255,GWAS_ID_8256,GWAS_ID_8257 RMVar_hsa_circ_86759,RMVar_hsa_circ_258744 69017 RMVar_ID_69017 Human_SNP_ID_411804649 m1A Human chr9 + 111896946 111896946 111896946 CGAGGCTCGGGAGAGGCGAACCGGAGCGCGGGACCGCGGTCGCCCCGACCAGAGCCGGGAGACCG CGAGGCTCGGGAGAGGCGAACCGGAGCGCGGGGCCGCGGTCGCCCCGACCAGAGCCGGGAGACCG A G UGCG Ensembl:ENSG00000148154 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:111896846..111897025 26863410 MeRIP-seq:(Medium) rs7871397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036983,Human_RBP_ID_5154437,Human_RBP_ID_5329585,Human_RBP_ID_22118805,Human_RBP_ID_23094345,Human_RBP_ID_26361960 GWAS_ID_8235,GWAS_ID_8236,GWAS_ID_8237,GWAS_ID_8238,GWAS_ID_8239,GWAS_ID_8240,GWAS_ID_8241,GWAS_ID_8242,GWAS_ID_8243,GWAS_ID_8244,GWAS_ID_8245,GWAS_ID_8246,GWAS_ID_8247,GWAS_ID_8248,GWAS_ID_8249,GWAS_ID_8250,GWAS_ID_8251,GWAS_ID_8252,GWAS_ID_8253,GWAS_ID_8254,GWAS_ID_8255,GWAS_ID_8256,GWAS_ID_8257 RMVar_hsa_circ_86759,RMVar_hsa_circ_258744 69018 RMVar_ID_69018 Human_SNP_ID_411804771 m1A Human chr9 - 111897152 111897151 111897152 GCGGCCGCCAACACGGACAACGCTCCCGCAGGAGGAGGACAGGGTGGGCGCCCGGTGCGGGGGCG GCGGCCGCCAACACGGACAACGCTCCCGCAGG_GGAGGACAGGGTGGGCGCCCGGTGCGGGGGCG CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:111897107..111897263 26863196 MeRIP-seq:(Medium) rs1305548149 Functional Loss DEL dbSNP153 33..33 33 - - - 69019 RMVar_ID_69019 Human_SNP_ID_411869214 m1A Human chr9 - 112157609 112157609 112157609 TTTCTGAAACATACAATTTATGATTCAGGTTTAGACGTCTGTGCCACTTGCCATGAACATGCCAC TTTCTGAAACATACAATTTATGATTCAGGTTTGGACGTCTGTGCCACTTGCCATGAACATGCCAC T C SUSD1 Ensembl:ENSG00000106868 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:112157521..112157649 26863196 MeRIP-seq:(Medium) rs747628967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036327 Human_Splice_Rec_1071858,Human_Splice_Rec_1071890,Human_Splice_Rec_1071920,Human_Splice_Rec_1071950 RMVar_hsa_circ_46547,RMVar_hsa_circ_258756,RMVar_hsa_circ_345103,RMVar_hsa_circ_258759,RMVar_hsa_circ_296454,RMVar_hsa_circ_258760,RMVar_hsa_circ_277797,RMVar_hsa_circ_258771,RMVar_hsa_circ_275023,RMVar_hsa_circ_335367,RMVar_hsa_circ_258772,RMVar_hsa_circ_258779,RMVar_hsa_circ_306155,RMVar_hsa_circ_258785,RMVar_hsa_circ_353801,RMVar_hsa_circ_286550,RMVar_hsa_circ_258786,RMVar_hsa_circ_258791,RMVar_hsa_circ_258789,RMVar_hsa_circ_282685,RMVar_hsa_circ_312611,RMVar_hsa_circ_258794,RMVar_hsa_circ_272338,RMVar_hsa_circ_258795 69020 RMVar_ID_69020 Human_SNP_ID_411873492 m1A Human chr9 - 112175073 112175073 112175073 CGGCCGGCGGGGCCCCCGGCTGGGCCTCGAGGACTCTGGGCGCACGGACGCTTCCCCGCCCCTGG CGGCCGGCGGGGCCCCCGGCTGGGCCTCGAGGGCTCTGGGCGCACGGACGCTTCCCCGCCCCTGG T C SUSD1 Ensembl:ENSG00000106868 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:112175067..112175255 26863196 MeRIP-seq:(Medium) rs1228190393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26795882 69021 RMVar_ID_69021 Human_SNP_ID_411896111 m1A Human chr9 - 112262526 112262526 112262526 AGGAAGCCTGGCCCTTTCTGGAGGTCCTTCCAATGAAGGCACAGTCCTACCTGGGCAGAGCCCTG AGGAAGCCTGGCCCTTTCTGGAGGTCCTTCCAGTGAAGGCACAGTCCTACCTGGGCAGAGCCCTG T C PTBP3 Ensembl:ENSG00000119314 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:112262476..112262525 32194978 MeRIP-seq:(Medium) rs771097183 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_709401,Human_RBP_ID_17437149,Human_RBP_ID_17550745,Human_RBP_ID_18127854,Human_RBP_ID_18902311,Human_RBP_ID_26198511 Human_Splice_Rec_1072024,Human_Splice_Rec_1072025,Human_Splice_Rec_1072052,Human_Splice_Rec_1072053,Human_Splice_Rec_1072078,Human_Splice_Rec_1072079,Human_Splice_Rec_1072106,Human_Splice_Rec_1072107,Human_Splice_Rec_1072130,Human_Splice_Rec_1072131,Human_Splice_Rec_1072152,Human_Splice_Rec_1072160 Human_miRNA_ID_2195295,Human_miRNA_ID_2195296 RMVar_hsa_circ_258807,RMVar_hsa_circ_335599,RMVar_hsa_circ_301605,RMVar_hsa_circ_258796,RMVar_hsa_circ_363671,RMVar_hsa_circ_337391,RMVar_hsa_circ_31594,RMVar_hsa_circ_74546,RMVar_hsa_circ_258797,RMVar_hsa_circ_106257,RMVar_hsa_circ_376276,RMVar_hsa_circ_258803,RMVar_hsa_circ_69431,RMVar_hsa_circ_258802,RMVar_hsa_circ_346336,RMVar_hsa_circ_368049,RMVar_hsa_circ_375396,RMVar_hsa_circ_363342,RMVar_hsa_circ_258806,RMVar_hsa_circ_258805,RMVar_hsa_circ_274057,RMVar_hsa_circ_279767,RMVar_hsa_circ_285015,RMVar_hsa_circ_328218,RMVar_hsa_circ_270519,RMVar_hsa_circ_258809,RMVar_hsa_circ_258810,RMVar_hsa_circ_258808,RMVar_hsa_circ_258818,RMVar_hsa_circ_258812,RMVar_hsa_circ_258814,RMVar_hsa_circ_303727,RMVar_hsa_circ_309865,RMVar_hsa_circ_326181,RMVar_hsa_circ_306337,RMVar_hsa_circ_284809,RMVar_hsa_circ_258813,RMVar_hsa_circ_273536,RMVar_hsa_circ_332363,RMVar_hsa_circ_374952,RMVar_hsa_circ_323463,RMVar_hsa_circ_258820,RMVar_hsa_circ_271013,RMVar_hsa_circ_258819,RMVar_hsa_circ_258816,RMVar_hsa_circ_258817 69022 RMVar_ID_69022 Human_SNP_ID_411905451 m1A Human chr9 + 112297848 112297848 112297848 AAAAAAAAAAACTCACCATACACACCTGTAGAAGGAGTAGAACTATTCATGGTAAAAGGTCCGTT AAAAAAAAAAACTCACCATACACACCTGTAGACGGAGTAGAACTATTCATGGTAAAAGGTCCGTT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:112297826..112297850 26863196 MeRIP-seq:(Medium) rs775927248 Functional Loss SNV dbSNP153 33..33 33 - - - 69023 RMVar_ID_69023 Human_SNP_ID_411905482 m1A Human chr9 - 112297918 112297918 112297918 GGTTTATTAACCAAACATTGGTTTTGCTTTTCAGCGGGGATCTGATGAGCTTCTTTCTTCTGGCA GGTTTATTAACCAAACATTGGTTTTGCTTTTCGGCGGGGATCTGATGAGCTTCTTTCTTCTGGCA T C PTBP3 Ensembl:ENSG00000119314 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:112297886..112297958;chr9:112297876..112297983 26863196 MeRIP-seq:(Medium) rs1463813548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965154,Human_RBP_ID_5036990,Human_RBP_ID_22628096 Human_Splice_Rec_1072019,Human_Splice_Rec_1072047,Human_Splice_Rec_1072073,Human_Splice_Rec_1072101,Human_Splice_Rec_1072127,Human_Splice_Rec_1072155,Human_Splice_Rec_1072165 RMVar_hsa_circ_301605,RMVar_hsa_circ_31594,RMVar_hsa_circ_106257,RMVar_hsa_circ_258803,RMVar_hsa_circ_368049,RMVar_hsa_circ_328218,RMVar_hsa_circ_258814,RMVar_hsa_circ_326181,RMVar_hsa_circ_323463,RMVar_hsa_circ_258820,RMVar_hsa_circ_377625,RMVar_hsa_circ_258824,RMVar_hsa_circ_258827,RMVar_hsa_circ_327185,RMVar_hsa_circ_337643 69024 RMVar_ID_69024 Human_SNP_ID_411915378 m1A Human chr9 - 112333460 112333460 112333460 GCCTCCATCTGGGCCATGGATGGGTAAGTACTAGGCGGCGCGGCGGCCGCACCGGGTTGCCTTGG GCCTCCATCTGGGCCATGGATGGGTAAGTACTTGGCGGCGCGGCGGCCGCACCGGGTTGCCTTGG T A PTBP3 Ensembl:ENSG00000119314 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:112333451..112333475 26863196 MeRIP-seq:(Medium) rs765832795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9339015,Human_RBP_ID_19145537 69025 RMVar_ID_69025 Human_SNP_ID_411927339 m1A Human chr9 - 112380133 112380121 112380133 ATGACTTTCGTAGATCAGAGGAGGTGGCGGCGACAGCGGCGGCGGCGAGCAGAGAGCTAAAGCTG ATGACTTTCGTAGATCAGAGGAGGTGGCGGCG____________GCGAGCAGAGAGCTAAAGCTG CCGCCGCCGCTGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:112380089..112380306 26863196 MeRIP-seq:(Medium) rs1251176670 Functional Loss DEL dbSNP153 33..44 33 - - - 69026 RMVar_ID_69026 Human_SNP_ID_411952723 m1A Human chr9 - 112486980 112486979 112486980 GGGAGGAGAGCGGCCAGAGGGCCGGGCACCAAAGGTAAGTGGAGCGGGGAAGGCGCCCGGCGGGC GGGAGGAGAGCGGCCAGAGGGCCGGGCACCAA_GGTAAGTGGAGCGGGGAAGGCGCCCGGCGGGC CT C C9orf147 Ensembl:ENSG00000230185 lincRNA exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:112486889..112486981 26863410 MeRIP-seq:(Medium) rs1564144930 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1072249 69027 RMVar_ID_69027 Human_SNP_ID_411952724 m1A Human chr9 - 112486981 112486981 112486981 CGGGAGGAGAGCGGCCAGAGGGCCGGGCACCAAAGGTAAGTGGAGCGGGGAAGGCGCCCGGCGGG CGGGAGGAGAGCGGCCAGAGGGCCGGGCACCAGAGGTAAGTGGAGCGGGGAAGGCGCCCGGCGGG T C C9orf147 Ensembl:ENSG00000230185 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:112486882..112486981 26863410 MeRIP-seq:(Medium) rs1338545590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1072249 69028 RMVar_ID_69028 Human_SNP_ID_411952738 m1A Human chr9 - 112486995 112486995 112486995 AAGGGGCGCGAGGGCGGGAGGAGAGCGGCCAGAGGGCCGGGCACCAAAGGTAAGTGGAGCGGGGA AAGGGGCGCGAGGGCGGGAGGAGAGCGGCCAGGGGGCCGGGCACCAAAGGTAAGTGGAGCGGGGA T C C9orf147 Ensembl:ENSG00000230185 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:112486883..112487062 26863196 MeRIP-seq:(Medium) rs1317866575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1072249 69029 RMVar_ID_69029 Human_SNP_ID_412016274 m1A Human chr9 + 112750822 112750797 112750822 GCTCGGGCGCGGAGCGGGGGCGCGCGGCGCGGAGCGGAGCGTCTGAGCGCCGGCAGAGACCAGCC GCTCGGGC_________________________GCGGAGCGTCTGAGCGCCGGCAGAGACCAGCC CGCGGAGCGGGGGCGCGCGGCGCGGA C SNX30 Ensembl:ENSG00000148158 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:112750759..112804844 26863196 MeRIP-seq:(Medium) rs1398415837 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_5006591 69030 RMVar_ID_69030 Human_SNP_ID_412016289 m1A Human chr9 + 112750822 112750822 112750822 GCTCGGGCGCGGAGCGGGGGCGCGCGGCGCGGAGCGGAGCGTCTGAGCGCCGGCAGAGACCAGCC GCTCGGGCGCGGAGCGGGGGCGCGCGGCGCGGCGCGGAGCGTCTGAGCGCCGGCAGAGACCAGCC A C SNX30 Ensembl:ENSG00000148158 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:112750759..112804844 26863196 MeRIP-seq:(Medium) rs1346835057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5006591 69031 RMVar_ID_69031 Human_SNP_ID_412017387 m1A Human chr9 + 112755284 112755282 112755285 AGGAGGTGAGGGAGTTAGTGGGTGAGTATCTGAAGAAGACTGTCCGGGGAGGGACTGCCTGAAGC AGGAGGTGAGGGAGTTAGTGGGTGAGTATCT___GAAGACTGTCCGGGGAGGGACTGCCTGAAGC TGAA T SNX30 Ensembl:ENSG00000148158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:112755282..112755398 26863196 MeRIP-seq:(Medium) rs1457021126 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5228879 69032 RMVar_ID_69032 Human_SNP_ID_412090462 m1A Human chr9 - 113053031 113053031 113053031 TGGAAGAAGAGGTTGCTGACCTCATGAAAAAGAGAGGCAAGGGTGTTGAATGGCTCTTCCACGTT TGGAAGAAGAGGTTGCTGACCTCATGAAAAAGCGAGGCAAGGGTGTTGAATGGCTCTTCCACGTT T G ZFP37 Ensembl:ENSG00000136866 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113053029..113053292 26863196 MeRIP-seq:(Medium) rs1355943147 Functional Loss SNV dbSNP153 33..33 33 - - - 69033 RMVar_ID_69033 Human_SNP_ID_412090703 m1A Human chr9 - 113054398 113054398 113054398 AGATTGGCTCGGGTCACCTAGGAAGAGAAGACAGATAGGGAAGAGAAGAGAGCCAGGGACAGAGG AGATTGGCTCGGGTCACCTAGGAAGAGAAGACCGATAGGGAAGAGAAGAGAGCCAGGGACAGAGG T G ZFP37 Ensembl:ENSG00000136866 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113054308..113054428 26863196 MeRIP-seq:(Medium) rs986817977 Functional Loss SNV dbSNP153 33..33 33 - - - 69034 RMVar_ID_69034 Human_SNP_ID_412125308 m1A Human chr9 + 113221590 113221590 113221590 GGTGGCGGTGGTGGACACGTCGAGCCGGGTAGAAGTGGAGGGGCCGTTCGAAGAGTCGTGAGGGG GGTGGCGGTGGTGGACACGTCGAGCCGGGTAGGAGTGGAGGGGCCGTTCGAAGAGTCGTGAGGGG A G SLC31A1 Ensembl:ENSG00000136868 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113221526..113227310 26863196 MeRIP-seq:(Medium) rs541190786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1337508,Human_RBP_ID_5006758,Human_RBP_ID_5123957,Human_RBP_ID_5329589,Human_RBP_ID_8944696,Human_RBP_ID_22466172,Human_RBP_ID_24280643 Human_Splice_Rec_1072649,Human_Splice_Rec_1072657 RMVar_hsa_circ_258888,RMVar_hsa_circ_112707 69035 RMVar_ID_69035 Human_SNP_ID_412125309 m1A Human chr9 + 113221590 113221590 113221590 GGTGGCGGTGGTGGACACGTCGAGCCGGGTAGAAGTGGAGGGGCCGTTCGAAGAGTCGTGAGGGG GGTGGCGGTGGTGGACACGTCGAGCCGGGTAGTAGTGGAGGGGCCGTTCGAAGAGTCGTGAGGGG A T SLC31A1 Ensembl:ENSG00000136868 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113221526..113227310 26863196 MeRIP-seq:(Medium) rs541190786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1337508,Human_RBP_ID_5006758,Human_RBP_ID_5123957,Human_RBP_ID_5329589,Human_RBP_ID_8944696,Human_RBP_ID_22466172,Human_RBP_ID_24280643 Human_Splice_Rec_1072649,Human_Splice_Rec_1072657 RMVar_hsa_circ_258888,RMVar_hsa_circ_112707 69036 RMVar_ID_69036 Human_SNP_ID_412125339 m1A Human chr9 + 113221676 113221676 113221676 AGAGAGGTGCTAGTGGCTGGACTTGACCTGGAAAGGTAAGGCTTCTCTCGGCCCCTCTTTCGCAC AGAGAGGTGCTAGTGGCTGGACTTGACCTGGACAGGTAAGGCTTCTCTCGGCCCCTCTTTCGCAC A C SLC31A1 Ensembl:ENSG00000136868 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:113221545..113221700 26863196 MeRIP-seq:(Medium) rs1452745271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965304,Human_RBP_ID_5037001,Human_RBP_ID_5123957,Human_RBP_ID_5329589,Human_RBP_ID_5409703,Human_RBP_ID_8944636,Human_RBP_ID_22466959 Human_Splice_Rec_1072649,Human_Splice_Rec_1072657 RMVar_hsa_circ_258888,RMVar_hsa_circ_112707 69037 RMVar_ID_69037 Human_SNP_ID_412137499 m1A Human chr9 - 113275399 113275399 113275399 TTGGGGGGGAGCCGAGGTTCCGGGAAGGGGCTAGGCCGGCTTGAAAAGAGGTAGGTGAGTCGACT TTGGGGGGGAGCCGAGGTTCCGGGAAGGGGCTGGGCCGGCTTGAAAAGAGGTAGGTGAGTCGACT T C CDC26 Ensembl:ENSG00000176386 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:113275392..113275491 32194978 MeRIP-seq:(Medium) rs950550283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268576,Human_RBP_ID_5035818,Human_RBP_ID_5408514,Human_RBP_ID_23216708 Human_Splice_Rec_1072659,Human_Splice_Rec_1072667 69038 RMVar_ID_69038 Human_SNP_ID_412137538 m1A Human chr9 - 113275521 113275521 113275521 TGGCATTGAGGGGCATCCCTCCTAGAACCTCCAGGAAAAGCTCGCGGAAGACGAGGTTCTGCGGA TGGCATTGAGGGGCATCCCTCCTAGAACCTCCGGGAAAAGCTCGCGGAAGACGAGGTTCTGCGGA T C CDC26 Ensembl:ENSG00000176386 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:113275269..113275575;chr9:113273352..113275575;chr9:113273376..113275575 26863196 MeRIP-seq:(Medium) rs867677453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5006859,Human_RBP_ID_16547022,Human_RBP_ID_26360971 69039 RMVar_ID_69039 Human_SNP_ID_412137931 m1A Human chr9 + 113276639 113276639 113276639 CTATTATGGAAGTTTGGAAGAGAAGGAGAGGGAGCGTCTGGCCAAAGGAGAGTCTGGGATTTTGG CTATTATGGAAGTTTGGAAGAGAAGGAGAGGGGGCGTCTGGCCAAAGGAGAGTCTGGGATTTTGG A G PRPF4 Ensembl:ENSG00000136875 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113276517..113276638 26863196 MeRIP-seq:(Medium) rs759807240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036344,Human_RBP_ID_7890207,Human_RBP_ID_8694783,Human_RBP_ID_16547023,Human_RBP_ID_26360972 Human_Splice_Rec_1072674,Human_Splice_Rec_1072675,Human_Splice_Rec_1072700,Human_Splice_Rec_1072701 RMVar_hsa_circ_73066 69040 RMVar_ID_69040 Human_SNP_ID_412138525 m1A Human chr9 - 113279000 113279000 113279000 ATCTGCCGGGCTCGCTTCCTTCTCTCAAACTCAGCCAATACTTCTGCCTGTCGCTCGCTGATATG ATCTGCCGGGCTCGCTTCCTTCTCTCAAACTCGGCCAATACTTCTGCCTGTCGCTCGCTGATATG T C RF00017-4706 RNACentral:URS0000954994 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:113278899..113279022 26863196 MeRIP-seq:(Medium) rs1188846334 Functional Loss SNV dbSNP153 33..33 33 - - - 69041 RMVar_ID_69041 Human_SNP_ID_412153851 m1A Human chr9 - 113340225 113340225 113340225 CGCGTTCCCGCCGGCCCCAGCTCCAGCCCCGCAGCCCACCGGTGGGTACTGAGCCTGAGGTGGGA CGCGTTCCCGCCGGCCCCAGCTCCAGCCCCGCTGCCCACCGGTGGGTACTGAGCCTGAGGTGGGA T A WDR31 Ensembl:ENSG00000148225 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:113340203..113340316 26863196 MeRIP-seq:(Medium) rs572930037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24280758 Human_Splice_Rec_1072753,Human_Splice_Rec_1072773,Human_Splice_Rec_1072793,Human_Splice_Rec_1072813,Human_Splice_Rec_1072833,Human_Splice_Rec_1072851 69042 RMVar_ID_69042 Human_SNP_ID_412166211 m1A Human chr9 + 113386891 113386888 113386891 CCATCTCAGTAAATGGCCCATCAGCCACCCAGAAGGTCAAGCCAGATTCATCCTTCACATCGAAT CCATCTCAGTAAATGGCCCATCAGCCACCC___AGGTCAAGCCAGATTCATCCTTCACATCGAAT CAGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:113386843..113386983 26863196 MeRIP-seq:(Medium) rs149591017 Functional Loss DEL dbSNP153 31..33 33 - - - 69043 RMVar_ID_69043 Human_SNP_ID_412166223 m1A Human chr9 + 113386945 113386945 113386945 TCACATCGAATCTACCTTCTAAACACATCCACAATCCATTCCCCTTTCTCCATCCCCACTGTCCC TCACATCGAATCTACCTTCTAAACACATCCACGATCCATTCCCCTTTCTCCATCCCCACTGTCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113386895..113387057 26863196 MeRIP-seq:(Medium) rs200599371 Functional Loss SNV dbSNP153 33..33 33 - - - 69044 RMVar_ID_69044 Human_SNP_ID_412168218 m1A Human chr9 - 113393590 113393590 113393590 GCCAATGCCCCAGGAGCCCTCGGTTCCAACCAACTGATGCCCCTGTGCCCACTGGCCCACGCCAT GCCAATGCCCCAGGAGCCCTCGGTTCCAACCAGCTGATGCCCCTGTGCCCACTGGCCCACGCCAT T C ALAD Ensembl:ENSG00000148218 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:113393539..113393619 26863196 MeRIP-seq:(Medium) rs1047941673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5038348 Human_Splice_Rec_1072890,Human_Splice_Rec_1072912,Human_Splice_Rec_1072934,Human_Splice_Rec_1072946,Human_Splice_Rec_1072952,Human_Splice_Rec_1072964,Human_Splice_Rec_1072968,Human_Splice_Rec_1072970 RMVar_hsa_circ_97594,RMVar_hsa_circ_258906,RMVar_hsa_circ_349322,RMVar_hsa_circ_367235 69045 RMVar_ID_69045 Human_SNP_ID_412169972 m1A Human chr9 + 113401248 113401248 113401248 CTCCCTAAGGGCTCCCGGCCGCTGCTCCTGTCACCGCTGTCTCCCGCTCCGGTCTCCCACAGACC CTCCCTAAGGGCTCCCGGCCGCTGCTCCTGTCGCCGCTGTCTCCCGCTCCGGTCTCCCACAGACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113401128..113401247 26863196 MeRIP-seq:(Medium) rs1205761624 Functional Loss SNV dbSNP153 33..33 33 - - - 69046 RMVar_ID_69046 Human_SNP_ID_412171879 m1A Human chr9 - 113408842 113408840 113408843 TGATGAAGACGAAGAAAGGCTGGAAGAAGAAGAACAGAATGAAGAGGAAGAAGTAGACAACTGAA TGATGAAGACGAAGAAAGGCTGGAAGAAGAA___CAGAATGAAGAGGAAGAAGTAGACAACTGAA GTTC G POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:113408701..113409756;chr9:113408651..113409675;chr9:113408676..113409727 26863196 MeRIP-seq:(Medium) rs761315806 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_92543,Human_RBP_ID_219732,Human_RBP_ID_1701281,Human_RBP_ID_2059673,Human_RBP_ID_3184550,Human_RBP_ID_7890335,Human_RBP_ID_9407210,Human_RBP_ID_16547450,Human_RBP_ID_17666341,Human_RBP_ID_18541896,Human_RBP_ID_18545071,Human_RBP_ID_22334552,Human_RBP_ID_23094347,Human_RBP_ID_23117259,Human_RBP_ID_24549634,Human_RBP_ID_24555416,Human_RBP_ID_26360976,Human_RBP_ID_27129234,Human_RBP_ID_27832609 69047 RMVar_ID_69047 Human_SNP_ID_412171889 m1A Human chr9 - 113408875 113408873 113408876 GGAAGAGCAAGACAAGAGCAGGGATGAGGACAATGATGAAGACGAAGAAAGGCTGGAAGAAGAAG GGAAGAGCAAGACAAGAGCAGGGATGAGGAC___GATGAAGACGAAGAAAGGCTGGAAGAAGAAG CATT C POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:113408776..113408975 26863196 MeRIP-seq:(Medium) rs3841000 Functional Loss DEL dbSNP153,HGVD 32..34 33 - - - Human_RBP_ID_92543,Human_RBP_ID_219732,Human_RBP_ID_1701281,Human_RBP_ID_2059673,Human_RBP_ID_5226898,Human_RBP_ID_7890335,Human_RBP_ID_8157092,Human_RBP_ID_8924780,Human_RBP_ID_9407210,Human_RBP_ID_16547450,Human_RBP_ID_17666341,Human_RBP_ID_17715716,Human_RBP_ID_18128192,Human_RBP_ID_18541897,Human_RBP_ID_18545071,Human_RBP_ID_23094347,Human_RBP_ID_23117259,Human_RBP_ID_24549634,Human_RBP_ID_26360976,Human_RBP_ID_27541319,Human_RBP_ID_27832609 69048 RMVar_ID_69048 Human_SNP_ID_412171891 m1A Human chr9 - 113408875 113408875 113408875 GGAAGAGCAAGACAAGAGCAGGGATGAGGACAATGATGAAGACGAAGAAAGGCTGGAAGAAGAAG GGAAGAGCAAGACAAGAGCAGGGATGAGGACAGTGATGAAGACGAAGAAAGGCTGGAAGAAGAAG T C POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:113408776..113408975 26863196 MeRIP-seq:(Medium) rs1473101189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92543,Human_RBP_ID_219732,Human_RBP_ID_1701281,Human_RBP_ID_2059673,Human_RBP_ID_5226898,Human_RBP_ID_7890335,Human_RBP_ID_8157092,Human_RBP_ID_8924780,Human_RBP_ID_9407210,Human_RBP_ID_16547450,Human_RBP_ID_17666341,Human_RBP_ID_17715716,Human_RBP_ID_18128192,Human_RBP_ID_18541897,Human_RBP_ID_18545071,Human_RBP_ID_23094347,Human_RBP_ID_23117259,Human_RBP_ID_24549634,Human_RBP_ID_26360976,Human_RBP_ID_27541319,Human_RBP_ID_27832609 69049 RMVar_ID_69049 Human_SNP_ID_412172164 m1A Human chr9 - 113409581 113409581 113409581 GAAGGTAACGAGCCTCTTGTCTTCTAAACCACATAGAAGATGGTCATCCTGTGTGACCTGTTCAC GAAGGTAACGAGCCTCTTGTCTTCTAAACCACGTAGAAGATGGTCATCCTGTGTGACCTGTTCAC T C POLE3 Ensembl:ENSG00000148229 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:113409579..113409660 26863196 MeRIP-seq:(Medium) rs371731372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19145563 69050 RMVar_ID_69050 Human_SNP_ID_412172493 m1A Human chr9 - 113410248 113410248 113410248 CCGAGGACCTAAACCTGCCCAATGCCGTGATCACCAGGATCATCAAGGAGGCGGTGAGCAGCTCG CCGAGGACCTAAACCTGCCCAATGCCGTGATCCCCAGGATCATCAAGGAGGCGGTGAGCAGCTCG T G POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:113410101..113410400 26863196 MeRIP-seq:(Medium) rs61733925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036348,Human_RBP_ID_8924781,Human_RBP_ID_9407213,Human_RBP_ID_16547459,Human_RBP_ID_17548084,Human_RBP_ID_18902501 Human_Splice_Rec_1072971,Human_Splice_Rec_1072975,Human_Splice_Rec_1072983 RMVar_hsa_circ_113544,RMVar_hsa_circ_258907 69051 RMVar_ID_69051 Human_SNP_ID_412185098 m1A Human chr9 + 113463807 113463807 113463807 GCTCCTGTCCGGGTCGCAGTGGGACGCCATGGAGCGCTCCCTGCACCGCGTCTCCCTCGGGAGCC GCTCCTGTCCGGGTCGCAGTGGGACGCCATGGCGCGCTCCCTGCACCGCGTCTCCCTCGGGAGCC A C RGS3 Ensembl:ENSG00000138835 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113463756..113463832 26863196 MeRIP-seq:(Medium) rs774757745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1073151,Human_Splice_Rec_1073195 RMVar_hsa_circ_109099,RMVar_hsa_circ_258908 69052 RMVar_ID_69052 Human_SNP_ID_412203788 m1A Human chr9 - 113542213 113542213 113542213 TCCCATCTCAGGGACTCTCCACGTGCTATTCCATCCACCGCGAACACTCTTCCCCAAGTCCAGGA TCCCATCTCAGGGACTCTCCACGTGCTATTCCGTCCACCGCGAACACTCTTCCCCAAGTCCAGGA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113542126..113542410 26863196 MeRIP-seq:(Medium) rs1475462098 Functional Loss SNV dbSNP153 33..33 33 - - - 69053 RMVar_ID_69053 Human_SNP_ID_412284176 m1A Human chr9 + 113876113 113876113 113876113 GGCCGCACGGCGAGGCCGGCCCGGGGGCGGGCAGGGCGGCGGGGGGCGGCGGCGGCCCCGCGAGG GGCCGCACGGCGAGGCCGGCCCGGGGGCGGGCGGGGCGGCGGGGGGCGGCGGCGGCCCCGCGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:113876059..113876211;chr9:113875956..113876129 26863196 MeRIP-seq:(Medium) rs1007156877 Functional Loss SNV dbSNP153 33..33 33 - - - 69054 RMVar_ID_69054 Human_SNP_ID_412284309 m1A Human chr9 - 113876313 113876313 113876313 TGCTCCTCCCGGGCCGGGCTGCTGGTGCGCGCACAATGCCGCCGCCGCCGCCGCCGCCGCCGCCG TGCTCCTCCCGGGCCGGGCTGCTGGTGCGCGCGCAATGCCGCCGCCGCCGCCGCCGCCGCCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:113876264..113876450 26863196 MeRIP-seq:(Medium) rs1262162939 Functional Loss SNV dbSNP153 33..33 33 - - - 69055 RMVar_ID_69055 Human_SNP_ID_412284327 m1A Human chr9 - 113876364 113876364 113876364 CGCCCGGCTGGTTCATGGGTCCGTGCGGGAGGAGGCGGCCCCGGCGCGTCCTGCTCCTCCCGGGC CGCCCGGCTGGTTCATGGGTCCGTGCGGGAGGCGGCGGCCCCGGCGCGTCCTGCTCCTCCCGGGC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:113876323..113876452 26863196 MeRIP-seq:(Medium) rs1404677250 Functional Loss SNV dbSNP153 33..33 33 - - - 69056 RMVar_ID_69056 Human_SNP_ID_412290139 m1A Human chr9 - 113900543 113900543 113900543 ACAGGAGCTCGGGTTCTGGCCTCAGCTCTGCCAGGTTCTCTTGGGTTGCTGCCTCACCTCAAAGA ACAGGAGCTCGGGTTCTGGCCTCAGCTCTGCCGGGTTCTCTTGGGTTGCTGCCTCACCTCAAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113900542..113900607 26863196 MeRIP-seq:(Medium) rs1328571704 Functional Loss SNV dbSNP153 33..33 33 - - - 69057 RMVar_ID_69057 Human_SNP_ID_412290198 m1A Human chr9 - 113900666 113900666 113900666 TAGGAGACAGCAGGTCGGGTTTGCGGGAGAGGACGGTGCTAGGAGACGGGAGCTCGGGTTCGCGG TAGGAGACAGCAGGTCGGGTTTGCGGGAGAGGGCGGTGCTAGGAGACGGGAGCTCGGGTTCGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113900659..113900769 26863196 MeRIP-seq:(Medium) rs1476352415 Functional Loss SNV dbSNP153 33..33 33 - - - 69058 RMVar_ID_69058 Human_SNP_ID_412297419 m1A Human chr9 - 113931245 113931245 113931245 CAGGGCAGGGACCACCTCATGCCTCTATGCTGAGTACACAGCAGGTGTTCCATGCTTATCACTGA CAGGGCAGGGACCACCTCATGCCTCTATGCTGGGTACACAGCAGGTGTTCCATGCTTATCACTGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:113931232..113931352 26863196 MeRIP-seq:(Medium) rs765910701 Functional Loss SNV dbSNP153 33..33 33 - - - 69059 RMVar_ID_69059 Human_SNP_ID_412297649 m1A Human chr9 + 113932271 113932271 113932271 CAATTGGTGGGGAACAGCATTCTAGGTGAGGGAACAGTGAGTGCAAAGGTTGGAATGAGCAGTAG CAATTGGTGGGGAACAGCATTCTAGGTGAGGGGACAGTGAGTGCAAAGGTTGGAATGAGCAGTAG A G ZNF618 Ensembl:ENSG00000157657 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:113932257..113932682 26863196 MeRIP-seq:(Medium) rs567977856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226902,Human_RBP_ID_24280906 69060 RMVar_ID_69060 Human_SNP_ID_412297651 m1A Human chr9 + 113932284 113932284 113932284 ACAGCATTCTAGGTGAGGGAACAGTGAGTGCAAAGGTTGGAATGAGCAGTAGAAAGGCCACAGTG ACAGCATTCTAGGTGAGGGAACAGTGAGTGCAGAGGTTGGAATGAGCAGTAGAAAGGCCACAGTG A G ZNF618 Ensembl:ENSG00000157657 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113932278..113932640 26863196 MeRIP-seq:(Medium) rs1036303086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226903,Human_RBP_ID_24280906 69061 RMVar_ID_69061 Human_SNP_ID_412297999 m1A Human chr9 + 113933852 113933852 113933852 TGGCTGGGGAGGGATAGCAGTGGGGGAGGGGCATGGCAGGGCAAGGGTGACAGGGTGGTGGATTG TGGCTGGGGAGGGATAGCAGTGGGGGAGGGGCGTGGCAGGGCAAGGGTGACAGGGTGGTGGATTG A G ZNF618 Ensembl:ENSG00000157657 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:113933848..113934153 26863196 MeRIP-seq:(Medium) rs1376676893 Functional Loss SNV dbSNP153 33..33 33 - - - 69062 RMVar_ID_69062 Human_SNP_ID_412298004 m1A Human chr9 - 113933867 113933867 113933867 CCCCCACAGGAGCTGCAATCCACCACCCTGTCACCCTTGCCCTGCCATGCCCCTCCCCCACTGCT CCCCCACAGGAGCTGCAATCCACCACCCTGTCCCCCTTGCCCTGCCATGCCCCTCCCCCACTGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113933858..113934107 26863196 MeRIP-seq:(Medium) rs1004767325 Functional Loss SNV dbSNP153 33..33 33 - - - 69063 RMVar_ID_69063 Human_SNP_ID_412357606 m1A Human chr9 - 114167835 114167835 114167835 GAGGCTCAGCACCAGTGCCAGCTCTGTGCCCAAGGCGGCAGGAATGACGGTGCCCGTGGGAGCCT GAGGCTCAGCACCAGTGCCAGCTCTGTGCCCAGGGCGGCAGGAATGACGGTGCCCGTGGGAGCCT T C lnc-KIF12-3 RNACentral:URS00008B4A3E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114167789..114167968 26863196 MeRIP-seq:(Medium) rs755425920 Functional Loss SNV dbSNP153 33..33 33 - - - 69064 RMVar_ID_69064 Human_SNP_ID_412358212 m1A Human chr9 + 114169159 114169159 114169159 CACTCCTGGCTCAGCTCCCACTGGAAGCAAGAAGCCCATTGGATCGGAAGCCTCAAAGAAAGCCG CACTCCTGGCTCAGCTCCCACTGGAAGCAAGAGGCCCATTGGATCGGAAGCCTCAAAGAAAGCCG A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114169112..114211016 32194978 MeRIP-seq:(Medium) rs1308219550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226906,Human_RBP_ID_18472687,Human_RBP_ID_19024111 RMVar_hsa_circ_50777,RMVar_hsa_circ_331270,RMVar_hsa_circ_92377,RMVar_hsa_circ_258936 69065 RMVar_ID_69065 Human_SNP_ID_412361618 m1A Human chr9 + 114182513 114182513 114182513 GATGGATGAGAAAAGATGCTGCCAGATGAGGGAACAGCATGGGCAAACGCAACGAGGAGAGAAAG GATGGATGAGAAAAGATGCTGCCAGATGAGGGTACAGCATGGGCAAACGCAACGAGGAGAGAAAG A T COL27A1 Ensembl:ENSG00000196739 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114182473..114182637 26863196 MeRIP-seq:(Medium) rs1016387504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50777,RMVar_hsa_circ_92377,RMVar_hsa_circ_258937,RMVar_hsa_circ_258936,RMVar_hsa_circ_322687 69066 RMVar_ID_69066 Human_SNP_ID_412361774 m1A Human chr9 - 114183066 114183066 114183066 CCACATCTCCAGCAAATACTCACTTTGGCTCCAGGAGGGCCGGGGAGACCTGGATTTCCATAAGG CCACATCTCCAGCAAATACTCACTTTGGCTCCCGGAGGGCCGGGGAGACCTGGATTTCCATAAGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:114178339..114194445 26863196 MeRIP-seq:(Medium) rs1307968839 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 69067 RMVar_ID_69067 Human_SNP_ID_412371099 m1A Human chr9 - 114222301 114222301 114222301 CACACGCTGGCTCCACCCTGAGTCTCCTCAACACCCACCTGCTGCCCCAGGCATCAATGTACTTA CACACGCTGGCTCCACCCTGAGTCTCCTCAACTCCCACCTGCTGCCCCAGGCATCAATGTACTTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114222288..114222405 26863196 MeRIP-seq:(Medium) rs759869629 Functional Loss SNV dbSNP153 33..33 33 - - - 69068 RMVar_ID_69068 Human_SNP_ID_412374377 m1A Human chr9 + 114235642 114235642 114235642 GGTTCCAGGTGTGTCAGGAGATCCCGGATTCCAAGGAGACAAGGTAATTGCATGAGATTTTCCCC GGTTCCAGGTGTGTCAGGAGATCCCGGATTCCGAGGAGACAAGGTAATTGCATGAGATTTTCCCC A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114235628..114245927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_847778,Human_RBP_ID_962171,Human_RBP_ID_5409803,Human_RBP_ID_5482400,Human_RBP_ID_5534907,Human_RBP_ID_8239219,Human_RBP_ID_9407227,Human_RBP_ID_18173172,Human_RBP_ID_18427357,Human_RBP_ID_18472703,Human_RBP_ID_19024150,Human_RBP_ID_22748004,Human_RBP_ID_23094760,Human_RBP_ID_23120852,Human_RBP_ID_26360425 Human_Splice_Rec_1073908,Human_Splice_Rec_1073909,Human_Splice_Rec_1074036,Human_Splice_Rec_1074037 RMVar_hsa_circ_18044,RMVar_hsa_circ_92377,RMVar_hsa_circ_258936,RMVar_hsa_circ_79983,RMVar_hsa_circ_114509,RMVar_hsa_circ_258938,RMVar_hsa_circ_35925,RMVar_hsa_circ_258939,RMVar_hsa_circ_31952,RMVar_hsa_circ_65651,RMVar_hsa_circ_341924 69069 RMVar_ID_69069 Human_SNP_ID_412378048 m1A Human chr9 - 114250631 114250631 114250631 CTCCCACGATTCCTGGCTCCCCGACCAGACCAATGAATCCCATAAATCCCTATGAGACACATTCC CTCCCACGATTCCTGGCTCCCCGACCAGACCAGTGAATCCCATAAATCCCTATGAGACACATTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114250619..114258577 32194978 MeRIP-seq:(Medium) rs764217880 Functional Loss SNV dbSNP153 33..33 33 - - - 69070 RMVar_ID_69070 Human_SNP_ID_412378523 m1A Human chr9 - 114252598 114252598 114252598 CCAGGCACGCCTGGGGGTCCCATCATGCCACGATCACCCTGTGATGGAGACAGCAATGCAGGCAG CCAGGCACGCCTGGGGGTCCCATCATGCCACGGTCACCCTGTGATGGAGACAGCAATGCAGGCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:114252593..114264387 26863196 MeRIP-seq:(Medium) rs369193268 Functional Loss SNV dbSNP153 33..33 33 - - - 69071 RMVar_ID_69071 Human_SNP_ID_412383360 m1A Human chr9 - 114270777 114270777 114270777 CCAGGCCCTGCCCTAAAAGGGCACTTACCTTCAGCCCATCAGGTCCCATGGGGCCACTGTCACCC CCAGGCCCTGCCCTAAAAGGGCACTTACCTTCTGCCCATCAGGTCCCATGGGGCCACTGTCACCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr9:114269096..114270832;chr9:114269281..114270843;chr9:114269181..114270815 26863196,32194978 MeRIP-seq:(Medium) rs1295195131 Functional Loss SNV dbSNP153 33..33 33 - - - 69072 RMVar_ID_69072 Human_SNP_ID_412387830 m1A Human chr9 + 114288740 114288740 114288740 GTGGGTGATCGAGGAGACCGCGGGGAACCGGGAGACCCTGGGTACCCTGTAAGTATCAGAGCTCC GTGGGTGATCGAGGAGACCGCGGGGAACCGGGGGACCCTGGGTACCCTGTAAGTATCAGAGCTCC A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1687410 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_847799,Human_RBP_ID_962188,Human_RBP_ID_5123968,Human_RBP_ID_5135283,Human_RBP_ID_5409847,Human_RBP_ID_5534955,Human_RBP_ID_8239365,Human_RBP_ID_9407259,Human_RBP_ID_18173192,Human_RBP_ID_18472738,Human_RBP_ID_19024217,Human_RBP_ID_22556157,Human_RBP_ID_23094646,Human_RBP_ID_23120915,Human_RBP_ID_24555423,Human_RBP_ID_26360446 Human_Splice_Rec_1073960,Human_Splice_Rec_1073961,Human_Splice_Rec_1074088,Human_Splice_Rec_1074089 GWAS_ID_8258,GWAS_ID_8259,GWAS_ID_8260,GWAS_ID_8261,GWAS_ID_8262,GWAS_ID_8263,GWAS_ID_8264,GWAS_ID_8265,GWAS_ID_8266 RMVar_hsa_circ_79983,RMVar_hsa_circ_258939,RMVar_hsa_circ_109166,RMVar_hsa_circ_258941 69073 RMVar_ID_69073 Human_SNP_ID_412391942 m1A Human chr9 + 114304615 114304615 114304615 CATACCCTGTCTTTTCCTTGCCCAGCAACAAGATGATCTTGGGGCAGCTTTCCAGACGTGGATGG CATACCCTGTCTTTTCCTTGCCCAGCAACAAGGTGATCTTGGGGCAGCTTTCCAGACGTGGATGG A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114301528..114306220 32194978 MeRIP-seq:(Medium) rs537785868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5535456,Human_RBP_ID_18173209 Human_Splice_Rec_1073988,Human_Splice_Rec_1073989,Human_Splice_Rec_1074116,Human_Splice_Rec_1074117 RMVar_hsa_circ_79983,RMVar_hsa_circ_258939,RMVar_hsa_circ_109166,RMVar_hsa_circ_258941,RMVar_hsa_circ_258942,RMVar_hsa_circ_121039 69074 RMVar_ID_69074 Human_SNP_ID_412393683 m1A Human chr9 + 114311308 114311308 114311308 TGCTACCTCCCACTGTGAAATCGCTGGTGCTCACAATTGTCTCTCACAGTGTATGTGATTTTTTT TGCTACCTCCCACTGTGAAATCGCTGGTGCTCGCAATTGTCTCTCACAGTGTATGTGATTTTTTT A G COL27A1 Ensembl:ENSG00000196739 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11537824 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8267 69075 RMVar_ID_69075 Human_SNP_ID_412393873 m1A Human chr9 - 114311961 114311961 114311961 CTTGACCCAAATTTACACTTGGAGCTAATGACAATGGGTTTCTACAGAATTTAATGACAATGAAA CTTGACCCAAATTTACACTTGGAGCTAATGACGATGGGTTTCTACAGAATTTAATGACAATGAAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114311911..114312011 32194978 MeRIP-seq:(Medium) rs371779493 Functional Loss SNV dbSNP153 33..33 33 - - - 69076 RMVar_ID_69076 Human_SNP_ID_412393952 m1A Human chr9 - 114312248 114312248 114312248 GGGCGGCAGGGCGAGGATACAGAAGTGTTGGGAGGGGGGACGGGCCAAAGTGAGGTATTAAATAA GGGCGGCAGGGCGAGGATACAGAAGTGTTGGGGGGGGGGACGGGCCAAAGTGAGGTATTAAATAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114312198..114312413 26863196 MeRIP-seq:(Medium) rs1250215201 Functional Loss SNV dbSNP153 33..33 33 - - - 69077 RMVar_ID_69077 Human_SNP_ID_412393992 m1A Human chr9 + 114312360 114312360 114312360 CTCATCTCAGCGCTCGGATCCCTCCTGCTGCCAGAATCCACTGGCCTCTGTCTCATTCTTGGGTT CTCATCTCAGCGCTCGGATCCCTCCTGCTGCCGGAATCCACTGGCCTCTGTCTCATTCTTGGGTT A G COL27A1 Ensembl:ENSG00000196739 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114312310..114312411 32194978 MeRIP-seq:(Medium) rs1030538058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_710018,Human_RBP_ID_5535478,Human_RBP_ID_18173258 69078 RMVar_ID_69078 Human_SNP_ID_412407425 m1A Human chr9 - 114359737 114359735 114359738 GAAGCCATGAGAATGGAGGAGGAGGAAGAAGGAGAGGAGGAGGAGGAGGAAGAGGGGGGAGGTGA GAAGCCATGAGAATGGAGGAGGAGGAAGAAG___AGGAGGAGGAGGAGGAAGAGGGGGGAGGTGA TCTC T AKNA Ensembl:ENSG00000106948 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114359657..114359739 26863196 MeRIP-seq:(Medium) rs761019569 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_268580 Human_Splice_Rec_1074194,Human_Splice_Rec_1074236,Human_Splice_Rec_1074296,Human_Splice_Rec_1074334,Human_Splice_Rec_1074380 RMVar_hsa_circ_66190,RMVar_hsa_circ_258950 69079 RMVar_ID_69079 Human_SNP_ID_412418448 m1A Human chr9 + 114402222 114402212 114402222 AGGGAAGCTGGGGCCTTGGGGTCCCCAGGGGCATGGGGAGGGAAATAAATAATAAACACCATGGG AGGGAAGCTGGGGCCTTGGGGTC__________TGGGGAGGGAAATAAATAATAAACACCATGGG CCCCAGGGGCA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:114402176..114402425 26863196 MeRIP-seq:(Medium) rs1315972385 Functional Loss DEL dbSNP153 24..33 33 - - - 69080 RMVar_ID_69080 Human_SNP_ID_412419839 m1A Human chr9 - 114406694 114406694 114406694 CGGCTCCACAGAACCGCAGCCCGCCAGCGGGCACCGCACCCACCCCAGGGACCTCCTCTGCACAG CGGCTCCACAGAACCGCAGCCCGCCAGCGGGCGCCGCACCCACCCCAGGGACCTCCTCTGCACAG T C WHRN Ensembl:ENSG00000095397 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114406508..114406759 26863196 MeRIP-seq:(Medium) rs1467059888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113886,RMVar_hsa_circ_258952 69081 RMVar_ID_69081 Human_SNP_ID_412420657 m1A Human chr9 + 114409726 114409726 114409726 TCTGCGACTCTTCTGCTTGGCTATCCATCCACAAGGCATGCTGTCGCTCACCTCCAAAACCTAAC TCTGCGACTCTTCTGCTTGGCTATCCATCCACGAGGCATGCTGTCGCTCACCTCCAAAACCTAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114409724..114409917 26863196 MeRIP-seq:(Medium) rs1270153318 Functional Loss SNV dbSNP153 33..33 33 - - - 69082 RMVar_ID_69082 Human_SNP_ID_412420677 m1A Human chr9 + 114409777 114409777 114409777 CTCCAAAACCTAACCCACCTGTCACCTGCTCGACAAGGTGTACCCTCACCACCTCAGCTAAAATC CTCCAAAACCTAACCCACCTGTCACCTGCTCGGCAAGGTGTACCCTCACCACCTCAGCTAAAATC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114409732..114409942 26863196 MeRIP-seq:(Medium) rs950888001 Functional Loss SNV dbSNP153 33..33 33 - - - 69083 RMVar_ID_69083 Human_SNP_ID_412422728 m1A Human chr9 + 114418709 114418709 114418709 GGCCTTTGCACATGCAGCTGCTTCTGTTGGAAATGCTCTTCTCCCAGATGTTGGCATGGCTCTCT GGCCTTTGCACATGCAGCTGCTTCTGTTGGAAGTGCTCTTCTCCCAGATGTTGGCATGGCTCTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114418664..114418808 26863196 MeRIP-seq:(Medium) rs889149486 Functional Loss SNV dbSNP153 33..33 33 - - - 69084 RMVar_ID_69084 Human_SNP_ID_412435906 m1A Human chr9 + 114472426 114472426 114472426 TCCAGCCACCTGGAGCACTCTGCCCAGATAGGACGGATCCGTGTATGATCATTTCCTTGTCAGCT TCCAGCCACCTGGAGCACTCTGCCCAGATAGGGCGGATCCGTGTATGATCATTTCCTTGTCAGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114472422..114472609 26863196 MeRIP-seq:(Medium) rs987091587 Functional Loss SNV dbSNP153 33..33 33 - - - 69085 RMVar_ID_69085 Human_SNP_ID_412464368 m1A Human chr9 + 114587849 114587849 114587849 TGCTCTCAGAATCGCTGCCGCCATGGCTAGTCAGTCTCAGGGGATTCAGCAGCTGCTGCAGGCCG TGCTCTCAGAATCGCTGCCGCCATGGCTAGTCCGTCTCAGGGGATTCAGCAGCTGCTGCAGGCCG A C ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1215471730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_710048,Human_RBP_ID_798729,Human_RBP_ID_1701310,Human_RBP_ID_5035829,Human_RBP_ID_7890865,Human_RBP_ID_8694951,Human_RBP_ID_8944637,Human_RBP_ID_9407276,Human_RBP_ID_16548342,Human_RBP_ID_26360462,Human_RBP_ID_27129321,Human_RBP_ID_27833311 Human_Splice_Rec_1074477 69086 RMVar_ID_69086 Human_SNP_ID_412464388 m1A Human chr9 + 114587885 114587885 114587885 TCAGGGGATTCAGCAGCTGCTGCAGGCCGAGAAGCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCA TCAGGGGATTCAGCAGCTGCTGCAGGCCGAGAGGCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCA A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:114587751..114587997 26863196 MeRIP-seq:(Medium) rs781231977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92478,Human_RBP_ID_5036349,Human_RBP_ID_8944637,Human_RBP_ID_9407276,Human_RBP_ID_16548343,Human_RBP_ID_19143761,Human_RBP_ID_26360462,Human_RBP_ID_27833311 Human_Splice_Rec_1074477 69087 RMVar_ID_69087 Human_SNP_ID_412464407 m1A Human chr9 + 114587918 114587918 114587918 GCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCAAAAGTGAGTTTCAGGGTGGGGCTGCCCGGCGTG GCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCACAAGTGAGTTTCAGGGTGGGGCTGCCCGGCGTG A C ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:114587751..114587983 26863196 MeRIP-seq:(Medium) rs1208370205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798219,Human_RBP_ID_5037453,Human_RBP_ID_8944637,Human_RBP_ID_19143761,Human_RBP_ID_26360462 Human_Splice_Rec_1074477 69088 RMVar_ID_69088 Human_SNP_ID_412465594 m1A Human chr9 - 114592499 114592499 114592499 TATATCAGGAAGTGGTTAAAAGTAGAAAAGCAAGCAGAGACAAGATGGTATATTATAACAATAAG TATATCAGGAAGTGGTTAAAAGTAGAAAAGCAGGCAGAGACAAGATGGTATATTATAACAATAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:114592495..114592699 26863196 MeRIP-seq:(Medium) rs1564274280 Functional Loss SNV dbSNP153 33..33 33 - - - 69089 RMVar_ID_69089 Human_SNP_ID_412466902 m1A Human chr9 + 114597594 114597594 114597594 ATCTCCAGGCATTGGGATCCCGTGGCAGTTGCAGCACTGAAGTGGAGAAGGAGACCCAGGAGAAG ATCTCCAGGCATTGGGATCCCGTGGCAGTTGCCGCACTGAAGTGGAGAAGGAGACCCAGGAGAAG A C ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:114592551..114597750 32194978 MeRIP-seq:(Medium) rs763968695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92480,Human_RBP_ID_710051,Human_RBP_ID_2059703,Human_RBP_ID_5038402,Human_RBP_ID_7890884,Human_RBP_ID_8694955,Human_RBP_ID_9407278,Human_RBP_ID_19143762,Human_RBP_ID_22118823,Human_RBP_ID_22466494,Human_RBP_ID_23117230,Human_RBP_ID_24281118,Human_RBP_ID_27129326,Human_RBP_ID_27833312 Human_Splice_Rec_1074480 Human_miRNA_ID_1514106,Human_miRNA_ID_1544543,Human_miRNA_ID_1597164 69090 RMVar_ID_69090 Human_SNP_ID_412466919 m1A Human chr9 + 114597619 114597619 114597619 CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCAGGAGAAGATGACCATCCTCCAGACATACTTCC CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCGGGAGAAGATGACCATCCTCCAGACATACTTCC A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114597551..114597632 26863196 MeRIP-seq:(Medium) rs145627791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2059703,Human_RBP_ID_7890884,Human_RBP_ID_9407278,Human_RBP_ID_18541899,Human_RBP_ID_19143762,Human_RBP_ID_22118823,Human_RBP_ID_22467003,Human_RBP_ID_23117230,Human_RBP_ID_26833429,Human_RBP_ID_27833312 Human_Splice_Rec_1074480 69091 RMVar_ID_69091 Human_SNP_ID_412466920 m1A Human chr9 + 114597619 114597619 114597619 CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCAGGAGAAGATGACCATCCTCCAGACATACTTCC CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCTGGAGAAGATGACCATCCTCCAGACATACTTCC A T ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114597551..114597632 26863196 MeRIP-seq:(Medium) rs145627791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2059703,Human_RBP_ID_7890884,Human_RBP_ID_9407278,Human_RBP_ID_18541899,Human_RBP_ID_19143762,Human_RBP_ID_22118823,Human_RBP_ID_22467003,Human_RBP_ID_23117230,Human_RBP_ID_26833429,Human_RBP_ID_27833312 Human_Splice_Rec_1074480 69092 RMVar_ID_69092 Human_SNP_ID_412470507 m1A Human chr9 + 114611515 114611515 114611515 GAGGCTGCGGCATTAGGGGCTCGGCGCCCCCGACCTTCCGCGTCCCGGGGTGGCGGCGGCGGCGG GAGGCTGCGGCATTAGGGGCTCGGCGCCCCCGGCCTTCCGCGTCCCGGGGTGGCGGCGGCGGCGG A G TMEM268 Ensembl:ENSG00000157693 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114611284..114611700 26863196 MeRIP-seq:(Medium) rs1010966542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256767,Human_RBP_ID_5037019 Human_Splice_Rec_1074483,Human_Splice_Rec_1074499,Human_Splice_Rec_1074515 69093 RMVar_ID_69093 Human_SNP_ID_412473113 m1A Human chr9 + 114621614 114621614 114621614 CGTCAGTTATGGTAGGTTTAGCAGAGGATTTGATCAGTTAGGAGTTTAGAGTGTCAAGGAGGCCT CGTCAGTTATGGTAGGTTTAGCAGAGGATTTGGTCAGTTAGGAGTTTAGAGTGTCAAGGAGGCCT A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114621604..114621871 26863196 MeRIP-seq:(Medium) rs1371896054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16548682 RMVar_hsa_circ_18112 69094 RMVar_ID_69094 Human_SNP_ID_412478679 m1A Human chr9 - 114644296 114644296 114644296 ATGTCAGTCCAGGAAAGAGCGTGAACTCATAAAGGGGTTTTGTGGGAGATGAAGCCAAAATCGCA ATGTCAGTCCAGGAAAGAGCGTGAACTCATAACGGGGTTTTGTGGGAGATGAAGCCAAAATCGCA T G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:114644248..114644350 26863196 MeRIP-seq:(Medium) rs1459690560 Functional Loss SNV dbSNP153 33..33 33 - - - 69095 RMVar_ID_69095 Human_SNP_ID_412595802 m1A Human chr9 - 115118059 115118059 115118059 ACAAAGGCAGCGCTGCTGGGGAACTCGGGGGAACGCGCACGTGGGAACCGCCGCAGCTCCACACT ACAAAGGCAGCGCTGCTGGGGAACTCGGGGGACCGCGCACGTGGGAACCGCCGCAGCTCCACACT T G TNC Ensembl:ENSG00000041982 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:115118035..115118123 26863410 MeRIP-seq:(Medium) rs1435170798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184143 Human_Splice_Rec_1074633,Human_Splice_Rec_1074687,Human_Splice_Rec_1074961 69096 RMVar_ID_69096 Human_SNP_ID_412861957 m1A Human chr9 + 116219948 116219948 116219948 TCTCCCTCTGCCTGCTTGCAGATGACGACTGTACGGACTCCTTCACGCCCAATCAAGTCGCCAGA TCTCCCTCTGCCTGCTTGCAGATGACGACTGTGCGGACTCCTTCACGCCCAATCAAGTCGCCAGA A G PAPPA Ensembl:ENSG00000182752 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:116219943..116220074 26863196 MeRIP-seq:(Medium) rs1378781982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1075028 Human_miRNA_ID_1504968 RMVar_hsa_circ_26790,RMVar_hsa_circ_92339,RMVar_hsa_circ_309679,RMVar_hsa_circ_80996,RMVar_hsa_circ_258988,RMVar_hsa_circ_294697,RMVar_hsa_circ_287094,RMVar_hsa_circ_78654,RMVar_hsa_circ_88049,RMVar_hsa_circ_49644,RMVar_hsa_circ_258994,RMVar_hsa_circ_99369,RMVar_hsa_circ_258991,RMVar_hsa_circ_258993,RMVar_hsa_circ_17167,RMVar_hsa_circ_258992,RMVar_hsa_circ_258990,RMVar_hsa_circ_277746,RMVar_hsa_circ_314354,RMVar_hsa_circ_326180,RMVar_hsa_circ_317205,RMVar_hsa_circ_306559,RMVar_hsa_circ_115267,RMVar_hsa_circ_258996,RMVar_hsa_circ_258998,RMVar_hsa_circ_259000,RMVar_hsa_circ_84852,RMVar_hsa_circ_258999,RMVar_hsa_circ_258997,RMVar_hsa_circ_258995,RMVar_hsa_circ_96662,RMVar_hsa_circ_10675,RMVar_hsa_circ_106538,RMVar_hsa_circ_311207,RMVar_hsa_circ_335091,RMVar_hsa_circ_259001,RMVar_hsa_circ_321672,RMVar_hsa_circ_102245,RMVar_hsa_circ_259003,RMVar_hsa_circ_259005,RMVar_hsa_circ_259007,RMVar_hsa_circ_96293,RMVar_hsa_circ_259006,RMVar_hsa_circ_259004,RMVar_hsa_circ_259002 69097 RMVar_ID_69097 Human_SNP_ID_412883151 m1A Human chr9 + 116309677 116309668 116309677 AGGGAGGAAAGAATCACATAATGGGGGCTGCGAGGGGTATATCCAAAAAAAGGTAAATAATAGAT AGGGAGGAAAGAATCACATAATGG_________GGGGTATATCCAAAAAAAGGTAAATAATAGAT GGGGCTGCGA G PAPPA Ensembl:ENSG00000182752 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:116309613..116309729 26863196 MeRIP-seq:(Medium) rs1469692432 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_83360,RMVar_hsa_circ_92339,RMVar_hsa_circ_78654,RMVar_hsa_circ_88049,RMVar_hsa_circ_258994,RMVar_hsa_circ_99369,RMVar_hsa_circ_258991,RMVar_hsa_circ_258993,RMVar_hsa_circ_258992,RMVar_hsa_circ_115267,RMVar_hsa_circ_258996,RMVar_hsa_circ_84852,RMVar_hsa_circ_258995,RMVar_hsa_circ_102245,RMVar_hsa_circ_259007,RMVar_hsa_circ_259009,RMVar_hsa_circ_81947,RMVar_hsa_circ_127541,RMVar_hsa_circ_259008,RMVar_hsa_circ_259014,RMVar_hsa_circ_126334,RMVar_hsa_circ_259013,RMVar_hsa_circ_25438,RMVar_hsa_circ_83630,RMVar_hsa_circ_92005,RMVar_hsa_circ_259017,RMVar_hsa_circ_259018,RMVar_hsa_circ_75638,RMVar_hsa_circ_371603,RMVar_hsa_circ_372316,RMVar_hsa_circ_85748,RMVar_hsa_circ_31260,RMVar_hsa_circ_259022,RMVar_hsa_circ_259024,RMVar_hsa_circ_259025,RMVar_hsa_circ_259023 69098 RMVar_ID_69098 Human_SNP_ID_412896960 m1A Human chr9 + 116369028 116369024 116369028 GCTGTCTCTTTTTCTGTCTTCATCTTACTCTCACTAATTTTTTTCCTATCTCTGTTTTTCCACTC GCTGTCTCTTTTTCTGTCTTCATCTTACT____CTAATTTTTTTCCTATCTCTGTTTTTCCACTC TCTCA T PAPPA Ensembl:ENSG00000182752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:116368987..116369155 26863196 MeRIP-seq:(Medium) rs545806228 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_92339,RMVar_hsa_circ_78654,RMVar_hsa_circ_88049,RMVar_hsa_circ_258994,RMVar_hsa_circ_258991,RMVar_hsa_circ_258993,RMVar_hsa_circ_258992,RMVar_hsa_circ_115267,RMVar_hsa_circ_102245,RMVar_hsa_circ_259007,RMVar_hsa_circ_372316,RMVar_hsa_circ_259025,RMVar_hsa_circ_29007,RMVar_hsa_circ_33814,RMVar_hsa_circ_327542,RMVar_hsa_circ_332413,RMVar_hsa_circ_259038,RMVar_hsa_circ_344244,RMVar_hsa_circ_35088,RMVar_hsa_circ_259041,RMVar_hsa_circ_259044,RMVar_hsa_circ_323891,RMVar_hsa_circ_303791,RMVar_hsa_circ_259045,RMVar_hsa_circ_105122,RMVar_hsa_circ_259047 69099 RMVar_ID_69099 Human_SNP_ID_412902139 m1A Human chr9 + 116389665 116389665 116389665 TTGTCACTGTGTCACTGGCAATTTCTTTGGCTAAGAACCCTCTTCTATTCATCCTCATGACTCAC TTGTCACTGTGTCACTGGCAATTTCTTTGGCTGAGAACCCTCTTCTATTCATCCTCATGACTCAC A G PAPPA Ensembl:ENSG00000182752 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:116389650..116389776 26863196 MeRIP-seq:(Medium) rs4836646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92339,RMVar_hsa_circ_258993,RMVar_hsa_circ_102245,RMVar_hsa_circ_259007,RMVar_hsa_circ_79577,RMVar_hsa_circ_259049 69100 RMVar_ID_69100 Human_SNP_ID_412902140 m1A Human chr9 + 116389665 116389665 116389665 TTGTCACTGTGTCACTGGCAATTTCTTTGGCTAAGAACCCTCTTCTATTCATCCTCATGACTCAC TTGTCACTGTGTCACTGGCAATTTCTTTGGCTTAGAACCCTCTTCTATTCATCCTCATGACTCAC A T PAPPA Ensembl:ENSG00000182752 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:116389650..116389776 26863196 MeRIP-seq:(Medium) rs4836646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92339,RMVar_hsa_circ_258993,RMVar_hsa_circ_102245,RMVar_hsa_circ_259007,RMVar_hsa_circ_79577,RMVar_hsa_circ_259049 69101 RMVar_ID_69101 Human_SNP_ID_412976086 m1A Human chr9 - 116687153 116687153 116687153 GGGTGAGCTTTCCTCTGAGAACCCGGGGCCTTAGCGACACGTAATCCAGTTTTCCGTCTCCTTGG GGGTGAGCTTTCCTCTGAGAACCCGGGGCCTTCGCGACACGTAATCCAGTTTTCCGTCTCCTTGG T G ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:116687102..116687209 26863196 MeRIP-seq:(Medium) rs906971229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1075139,Human_Splice_Rec_1075285 RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_123989,RMVar_hsa_circ_259054 69102 RMVar_ID_69102 Human_SNP_ID_412976303 m1A Human chr9 + 116687610 116687610 116687610 GCTGAGGAGATCCGAGGAGATGCAGCTGGGGGAGGGGAGCGAGGGGCTCTGAAGAGATTTGCGGT GCTGAGGAGATCCGAGGAGATGCAGCTGGGGGGGGGGAGCGAGGGGCTCTGAAGAGATTTGCGGT A G TRIM32 Ensembl:ENSG00000119401 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:116687575..116688232 26863196 MeRIP-seq:(Medium) rs1241330443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8223304,Human_RBP_ID_9442306 69103 RMVar_ID_69103 Human_SNP_ID_412976396 m1A Human chr9 + 116688007 116688007 116688007 GAGGTGTGAAGGCAGCACATGACATTCAGTGCATAAGAGGAAGGAGCAGGGTATGAGGGCAGCAC GAGGTGTGAAGGCAGCACATGACATTCAGTGCGTAAGAGGAAGGAGCAGGGTATGAGGGCAGCAC A G TRIM32 Ensembl:ENSG00000119401 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:116687977..116688139 26863196 MeRIP-seq:(Medium) rs754641107 Functional Loss SNV dbSNP153 33..33 33 - - - 69104 RMVar_ID_69104 Human_SNP_ID_412978452 m1A Human chr9 + 116697702 116697697 116697702 TGACCCTCTAGGGCATGAATACTGTGCTGTTCAGTTCTGAGCTGTGCTAGCAATACCCTTCAAAG TGACCCTCTAGGGCATGAATACTGTGCT_____GTTCTGAGCTGTGCTAGCAATACCCTTCAAAG TGTTCA T TRIM32 Ensembl:ENSG00000119401 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:116697673..116697763 26863196 MeRIP-seq:(Medium) rs1301084122 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_2059719,Human_RBP_ID_5036350 Human_Splice_Rec_1075324,Human_Splice_Rec_1075326,Human_Splice_Rec_1075330 69105 RMVar_ID_69105 Human_SNP_ID_412978454 m1A Human chr9 + 116697702 116697702 116697702 TGACCCTCTAGGGCATGAATACTGTGCTGTTCAGTTCTGAGCTGTGCTAGCAATACCCTTCAAAG TGACCCTCTAGGGCATGAATACTGTGCTGTTCTGTTCTGAGCTGTGCTAGCAATACCCTTCAAAG A T TRIM32 Ensembl:ENSG00000119401 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:116697673..116697763 26863196 MeRIP-seq:(Medium) rs201288003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2059719,Human_RBP_ID_5036350 Human_Splice_Rec_1075324,Human_Splice_Rec_1075326,Human_Splice_Rec_1075330 69106 RMVar_ID_69106 Human_SNP_ID_724866217 m1A Human chrX - 92113718 92113718 92113718 AAGGAAGAGTTGACCCTGGAGGGTATCCGCCAATTCTACATCAACGTGGAACGAGAGGAGTGGAA AAGGAAGAGTTGACCCTGGAGGGTATCCGCCAGTTCTACATCAACGTGGAACGAGAGGAGTGGAA T C EIF4A1P10 Ensembl:ENSG00000229132 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879093645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637984,Human_RBP_ID_18522295,Human_RBP_ID_22413482 69107 RMVar_ID_69107 Human_SNP_ID_724866324 m1A Human chrX - 92114325 92114325 92114325 TGACATGAACCTCTCGGAGTCCCTTCTCCGTGACATCTATGCCTATGGTTTTGAGAAGCCCTCTG TGACATGAACCTCTCGGAGTCCCTTCTCCGTGGCATCTATGCCTATGGTTTTGAGAAGCCCTCTG T C EIF4A1P10 Ensembl:ENSG00000229132 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878883651 Functional Loss SNV dbSNP153 33..33 33 - - - 69108 RMVar_ID_69108 Human_SNP_ID_725747584 m1A Human chrX + 96685137 96685137 96685137 AGGAACCCGGTGGGGGCCGGAGCAACAAGCGGAGCGCGGGGAACCGGGCCGCCAATGAAGAGGAA AGGAACCCGGTGGGGGCCGGAGCAACAAGCGGGGCGCGGGGAACCGGGCCGCCAATGAAGAGGAA A G DIAPH2 Ensembl:ENSG00000147202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:96684887..96685175 26863196 MeRIP-seq:(Medium) rs1020294222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23107269 Human_Splice_Rec_2222439,Human_Splice_Rec_2222488,Human_Splice_Rec_2222537,Human_Splice_Rec_2222585,Human_Splice_Rec_2222633 69109 RMVar_ID_69109 Human_SNP_ID_725810396 m1A Human chrX - 97052368 97052366 97052368 CATCTCCAACACGAACCTTGTAGTCTACCCACATGTTATATACCTACTATTGCCTGGGAATATGA CATCTCCAACACGAACCTTGTAGTCTACCCAC__GTTATATACCTACTATTGCCTGGGAATATGA CAT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:97052321..97052456 26863196 MeRIP-seq:(Medium) rs772069120 Functional Loss DEL dbSNP153 33..34 33 - - - 69110 RMVar_ID_69110 Human_SNP_ID_726442231 m1A Human chrX - 100636667 100636667 100636667 TAGTCATGGCGTCCCCGTCTCGGAGACTGCAGACTAAACCAGTCATTACTTGTTTCAAGAGCGTT TAGTCATGGCGTCCCCGTCTCGGAGACTGCAGTCTAAACCAGTCATTACTTGTTTCAAGAGCGTT T A TSPAN6 Ensembl:ENSG00000000003 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:100636612..100636712 32194978 MeRIP-seq:(Medium) rs143834660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_740698,Human_RBP_ID_800313,Human_RBP_ID_848239,Human_RBP_ID_1719913,Human_RBP_ID_5075709,Human_RBP_ID_5483668,Human_RBP_ID_16954625,Human_RBP_ID_24357091 Human_Splice_Rec_2222780 69111 RMVar_ID_69111 Human_SNP_ID_726442255 m1A Human chrX + 100636707 100636707 100636707 CTCCGAGACGGGGACGCCATGACTAGCCCGAGACCCTGCACCACCGCACCGGGCGATTGGAACAC CTCCGAGACGGGGACGCCATGACTAGCCCGAGTCCCTGCACCACCGCACCGGGCGATTGGAACAC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:100636651..100636725 26863196 MeRIP-seq:(Medium) rs1463369436 Functional Loss SNV dbSNP153 33..33 33 - - - 69112 RMVar_ID_69112 Human_SNP_ID_726472307 m1A Human chrX + 100822320 100822320 100822320 TATGGCTTCTGTGAATACCAAGACCAAGAGACAGCACTTAGTGCCATGCGGAACCTGAATGGGCG TATGGCTTCTGTGAATACCAAGACCAAGAGACGGCACTTAGTGCCATGCGGAACCTGAATGGGCG A G CSTF2 Ensembl:ENSG00000101811 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:100821512..100822425;chrX:100822225..100822375 26863196 MeRIP-seq:(Medium) rs778016639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723564,Human_RBP_ID_968414,Human_RBP_ID_16772067 Human_Splice_Rec_2223046,Human_Splice_Rec_2223073,Human_Splice_Rec_2223098,Human_Splice_Rec_2223123 Human_miRNA_ID_2134777,Human_miRNA_ID_2317190,Human_miRNA_ID_2320345,Human_miRNA_ID_2323499,Human_miRNA_ID_2326675,Human_miRNA_ID_2329760,Human_miRNA_ID_2521052,Human_miRNA_ID_2524220,Human_miRNA_ID_2776075,Human_miRNA_ID_2823400,Human_miRNA_ID_2829531,Human_miRNA_ID_2832688,Human_miRNA_ID_2836815,Human_miRNA_ID_2842163 RMVar_hsa_circ_98233,RMVar_hsa_circ_263264 69113 RMVar_ID_69113 Human_SNP_ID_726503701 m1A Human chrX - 101008938 101008938 101008938 GACACCAGGGTGGGCAGGAGGCAGAAGACAGAAGAGGGGAAGGTTTAGGCCACTGCCGTTACTTG GACACCAGGGTGGGCAGGAGGCAGAAGACAGACGAGGGGAAGGTTTAGGCCACTGCCGTTACTTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101008888..101009046 26863196 MeRIP-seq:(Medium) rs1207821999 Functional Loss SNV dbSNP153 33..33 33 - - - 69114 RMVar_ID_69114 Human_SNP_ID_726503924 m1A Human chrX - 101010402 101010402 101010402 CTGGTCTGAGGCAGATTTTTTTTTTGAGATAGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGTGG CTGGTCTGAGGCAGATTTTTTTTTTGAGATAGGGTCTCACTCTTGCCCAGGCTGGAGTGTCGTGG T C TRMT2B Ensembl:ENSG00000188917 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3207291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16772376 69115 RMVar_ID_69115 Human_SNP_ID_726526457 m1A Human chrX + 101135407 101135407 101135407 GTGATAGCAGAGATATGAGAAGATAAAAAAATAGAGGGTAGTATAGCTGGATAGTATGAACAAAG GTGATAGCAGAGATATGAGAAGATAAAAAAATGGAGGGTAGTATAGCTGGATAGTATGAACAAAG A G CENPI Ensembl:ENSG00000102384 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101135363..101135454 26863196 MeRIP-seq:(Medium) rs980064475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313447,RMVar_hsa_circ_331266,RMVar_hsa_circ_102613,RMVar_hsa_circ_263293,RMVar_hsa_circ_51334,RMVar_hsa_circ_263294,RMVar_hsa_circ_19101,RMVar_hsa_circ_268940,RMVar_hsa_circ_309892,RMVar_hsa_circ_369968,RMVar_hsa_circ_290050,RMVar_hsa_circ_263297,RMVar_hsa_circ_263298,RMVar_hsa_circ_263299,RMVar_hsa_circ_347190 69116 RMVar_ID_69116 Human_SNP_ID_726531989 m1A Human chrX - 101165691 101165691 101165691 TTTTGCTGGTTCCTCTTCTCCTCTACTTCTCAATGCTGGCATACCTTAGGTCTCTGTCTTTTGCT TTTTGCTGGTTCCTCTTCTCCTCTACTTCTCAGTGCTGGCATACCTTAGGTCTCTGTCTTTTGCT T C RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101165641..101165728 26863196 MeRIP-seq:(Medium) rs753273501 Functional Loss SNV dbSNP153 33..33 33 - - - 69117 RMVar_ID_69117 Human_SNP_ID_726548299 m1A Human chrX - 101262851 101262851 101262851 CCCGCCTAAGGCTTAGGCAGGCATATGCCTCCAAAGTCCTTGAGCCCTCCGTCCCACATTCCCGC CCCGCCTAAGGCTTAGGCAGGCATATGCCTCCCAAGTCCTTGAGCCCTCCGTCCCACATTCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101262785..101262850 26863196 MeRIP-seq:(Medium) rs201818059 Functional Loss SNV dbSNP153 33..33 33 - - - 69118 RMVar_ID_69118 Human_SNP_ID_726563570 m1A Human chrX - 101343363 101343363 101343363 AAAATTAGCTGAGCATGGTGGCACATACCTGTAGTCCCAGATACATGGGAGGCTGAGGCGAGAGG AAAATTAGCTGAGCATGGTGGCACATACCTGTGGTCCCAGATACATGGGAGGCTGAGGCGAGAGG T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1448106153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7960930 69119 RMVar_ID_69119 Human_SNP_ID_726563587 m1A Human chrX - 101343504 101343504 101343504 AATTTAATGTGAGGCCAGGCACGGTGGCTCACATCTATAATCTCAGTACTTTGGGAGGCTGAAGT AATTTAATGTGAGGCCAGGCACGGTGGCTCACGTCTATAATCTCAGTACTTTGGGAGGCTGAAGT T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782603052 Functional Loss SNV dbSNP153 33..33 33 - - - 69120 RMVar_ID_69120 Human_SNP_ID_726563639 m1A Human chrX - 101343785 101343785 101343785 GTGTGCACTGATTATGTGGGGCCTTGTAGGCCATGGCAAGGACTTTGGGCTTTTACTAAGCAAGG GTGTGCACTGATTATGTGGGGCCTTGTAGGCCGTGGCAAGGACTTTGGGCTTTTACTAAGCAAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101343737..101343915 26863196 MeRIP-seq:(Medium) rs782456945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7960938,Human_RBP_ID_16774273,Human_RBP_ID_24318954 69121 RMVar_ID_69121 Human_SNP_ID_726564534 m1A Human chrX + 101348626 101348626 101348626 TCGATGAAATGCTGCAACTGCGGGTCCACTGCACCCAAACCCGCCGCGGAGGAAGAGGAGGAGGA TCGATGAAATGCTGCAACTGCGGGTCCACTGCCCCCAAACCCGCCGCGGAGGAAGAGGAGGAGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101348577..101348700 26863196 MeRIP-seq:(Medium) rs797044615 Functional Loss SNV dbSNP153 33..33 33 - - - 69122 RMVar_ID_69122 Human_SNP_ID_726572038 m1A Human chrX + 101391426 101391426 101391426 TAAGGTAGGGCGTTGTGCCATTGTGGTCAAATAACATTGCACGTTCTGAACTGTTTCTTTACTAG TAAGGTAGGGCGTTGTGCCATTGTGGTCAAATCACATTGCACGTTCTGAACTGTTTCTTTACTAG A C RPL36A-HNRNPH2,RPL36A Ensembl:ENSG00000257529,Ensembl:ENSG00000241343 Protein coding,Protein coding intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:101391423..101391762 26863410 MeRIP-seq:(Medium) rs369758384 Functional Loss SNV dbSNP153 33..33 33 - - - 69123 RMVar_ID_69123 Human_SNP_ID_726572039 m1A Human chrX + 101391429 101391429 101391429 GGTAGGGCGTTGTGCCATTGTGGTCAAATAACATTGCACGTTCTGAACTGTTTCTTTACTAGGTT GGTAGGGCGTTGTGCCATTGTGGTCAAATAACGTTGCACGTTCTGAACTGTTTCTTTACTAGGTT A G RPL36A-HNRNPH2,RPL36A Ensembl:ENSG00000257529,Ensembl:ENSG00000241343 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:101391425..101391725 26863410 MeRIP-seq:(Medium) rs1555983377 Functional Loss SNV dbSNP153 33..33 33 - - - 69124 RMVar_ID_69124 Human_SNP_ID_726574898 m1A Human chrX - 101403968 101403968 101403968 GAATTTCTCTTTCAGTGAGAAGCTCTTCATGGAGATGGCAGAGCTCATGGTCTCAGAAGGCTGGA GAATTTCTCTTTCAGTGAGAAGCTCTTCATGGGGATGGCAGAGCTCATGGTCTCAGAAGGCTGGA T C GLA Ensembl:ENSG00000102393 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs781927744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723789,Human_RBP_ID_966749,Human_RBP_ID_2067916,Human_RBP_ID_7961097,Human_RBP_ID_8276810,Human_RBP_ID_17717293,Human_RBP_ID_18142615,Human_RBP_ID_22693409,Human_RBP_ID_23096872 Human_Splice_Rec_2224007,Human_Splice_Rec_2224019,Human_Splice_Rec_2224033,Human_Splice_Rec_2224048,Human_Splice_Rec_2224060,Human_Splice_Rec_2224076,Human_Splice_Rec_2224090,Human_Splice_Rec_2224102 Clinvar_Rec_282 69125 RMVar_ID_69125 Human_SNP_ID_726575642 m1A Human chrX - 101407828 101407828 101407828 CGCTTCGCTTCCTGGCCCTCGTTTCCTGGGACATCCCTGGGGCTAGAGCACTGGACAATGGATTG CGCTTCGCTTCCTGGCCCTCGTTTCCTGGGACTTCCCTGGGGCTAGAGCACTGGACAATGGATTG T A GLA Ensembl:ENSG00000102393 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:101407779..101407887 26863196 MeRIP-seq:(Medium) rs869312397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723794,Human_RBP_ID_5045721,Human_RBP_ID_8931612,Human_RBP_ID_17717295,Human_RBP_ID_22468017,Human_RBP_ID_23107381,Human_RBP_ID_27377791 69126 RMVar_ID_69126 Human_SNP_ID_726575686 m1A Human chrX - 101407899 101407899 101407899 AAATTTATGCTGTCCGGTCACCGTGACAATGCAGCTGAGGAACCCAGAACTACATCTGGGCTGCG AAATTTATGCTGTCCGGTCACCGTGACAATGCGGCTGAGGAACCCAGAACTACATCTGGGCTGCG T C GLA Ensembl:ENSG00000102393 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782386191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723796,Human_RBP_ID_1709215,Human_RBP_ID_5077283,Human_RBP_ID_16774659 69127 RMVar_ID_69127 Human_SNP_ID_726575687 m1A Human chrX - 101407899 101407899 101407899 AAATTTATGCTGTCCGGTCACCGTGACAATGCAGCTGAGGAACCCAGAACTACATCTGGGCTGCG AAATTTATGCTGTCCGGTCACCGTGACAATGCCGCTGAGGAACCCAGAACTACATCTGGGCTGCG T G GLA Ensembl:ENSG00000102393 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782386191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723796,Human_RBP_ID_1709215,Human_RBP_ID_5077283,Human_RBP_ID_16774659 69128 RMVar_ID_69128 Human_SNP_ID_726576608 m1A Human chrX - 101412571 101412571 101412571 CTGCATAGCCATGAGCTTTCGAGGGGGATCATAGTGGGTTCGAACTTCAGCTCGGCTACTCTTGA CTGCATAGCCATGAGCTTTCGAGGGGGATCATCGTGGGTTCGAACTTCAGCTCGGCTACTCTTGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:101412453..101412701 32194978 MeRIP-seq:(Medium) rs782441397 Functional Loss SNV dbSNP153 33..33 33 - - - 69129 RMVar_ID_69129 Human_SNP_ID_726576633 m1A Human chrX - 101412687 101412687 101412687 TCATAGCCTCCATACCCTCCACCATAGGCACCACGCCTCATCCTTTCAAACCCAGCTCCTCTGCC TCATAGCCTCCATACCCTCCACCATAGGCACCTCGCCTCATCCTTTCAAACCCAGCTCCTCTGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:101412449..101412796;chrX:101412636..101412802 26863196 MeRIP-seq:(Medium) rs1569308061 Functional Loss SNV dbSNP153 33..33 33 - - - 69130 RMVar_ID_69130 Human_SNP_ID_726591071 m1A Human chrX - 101492256 101492256 101492256 TCCAATGGCCTGATTCCCAGCGAGAGCCCAAGACCCCCCACTGGCCTGGTTCTCAGCCCCAGTCC TCCAATGGCCTGATTCCCAGCGAGAGCCCAAGTCCCCCCACTGGCCTGGTTCTCAGCCCCAGTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101492207..101492410 26863196 MeRIP-seq:(Medium) rs1307842409 Functional Loss SNV dbSNP153 33..33 33 - - - 69131 RMVar_ID_69131 Human_SNP_ID_726591109 m1A Human chrX - 101492390 101492390 101492390 CAAGACCCTTCACTGGCTTGGTTCTCAGCCCCAGTCCAGGACCCTCCAATGGCCTCTTCCCCAAC CAAGACCCTTCACTGGCTTGGTTCTCAGCCCCCGTCCAGGACCCTCCAATGGCCTCTTCCCCAAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101492342..101492562 26863196 MeRIP-seq:(Medium) rs1292687951 Functional Loss SNV dbSNP153 33..33 33 - - - 69132 RMVar_ID_69132 Human_SNP_ID_726613465 m1A Human chrX - 101616495 101616495 101616495 GATGACAGTGAGAAGCTGGAGGAGGAGGGGGAAGAGGAGTGGGACGATGACCAGGAGCTGGATGA GATGACAGTGAGAAGCTGGAGGAGGAGGGGGAGGAGGAGTGGGACGATGACCAGGAGCTGGATGA T C ARMCX6 Ensembl:ENSG00000198960 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101616361..101616631 26863196 MeRIP-seq:(Medium) rs782245519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24319105 69133 RMVar_ID_69133 Human_SNP_ID_726613490 m1A Human chrX + 101616567 101616567 101616567 ATGGTCAGTTTGTAAACGCAGTAGCAGGCACCAGCCCCAATCATCAGTCCTGCCGCCATCCAACC ATGGTCAGTTTGTAAACGCAGTAGCAGGCACCCGCCCCAATCATCAGTCCTGCCGCCATCCAACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:101616311..101616650 26863196 MeRIP-seq:(Medium) rs1322090746 Functional Loss SNV dbSNP153 33..33 33 - - - 69134 RMVar_ID_69134 Human_SNP_ID_726613496 m1A Human chrX + 101616574 101616574 101616574 GTTTGTAAACGCAGTAGCAGGCACCAGCCCCAATCATCAGTCCTGCCGCCATCCAACCCACTTCC GTTTGTAAACGCAGTAGCAGGCACCAGCCCCAGTCATCAGTCCTGCCGCCATCCAACCCACTTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:101616359..101616905 26863196 MeRIP-seq:(Medium) rs1164489566 Functional Loss SNV dbSNP153 33..33 33 - - - 69135 RMVar_ID_69135 Human_SNP_ID_726615227 m1A Human chrX + 101626723 101626723 101626723 TGAATGGGGTAGGGTGGTTAGGGAATTCCATGAGACAAGACAAGGGGGGCATGGTGTGAGAAAGG TGAATGGGGTAGGGTGGTTAGGGAATTCCATGGGACAAGACAAGGGGGGCATGGTGTGAGAAAGG A G ARMCX3 Ensembl:ENSG00000102401 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:101626672..101626769;chrX:101626673..101626772 26863196 MeRIP-seq:(Medium) rs1569370939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24319149,Human_RBP_ID_26573876 RMVar_hsa_circ_263320 69136 RMVar_ID_69136 Human_SNP_ID_726615250 m1A Human chrX - 101626846 101626846 101626846 ATTCAAACAATTCTCCACAACTGGCTTCACCCAGCTTTCCAAAATTATCTACTCCCACTCTCCAC ATTCAAACAATTCTCCACAACTGGCTTCACCCTGCTTTCCAAAATTATCTACTCCCACTCTCCAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:101626795..101626946 32194978 MeRIP-seq:(Medium) rs1309789305 Functional Loss SNV dbSNP153 33..33 33 - - - 69137 RMVar_ID_69137 Human_SNP_ID_726806503 m1A Human chrX - 102890391 102890391 102890391 CTCTAATCTTGACACTCACAATACAATTATCCAAACTCCTTACAGGGCCCAAACCATGTGGCTCC CTCTAATCTTGACACTCACAATACAATTATCCGAACTCCTTACAGGGCCCAAACCATGTGGCTCC T C lnc-BEX1-3 RNACentral:URS00008B6E52 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:102890342..102890441 26863196 MeRIP-seq:(Medium) rs1412251203 Functional Loss SNV dbSNP153 33..33 33 - - - 69138 RMVar_ID_69138 Human_SNP_ID_726881832 m1A Human chrX + 103309758 103309758 103309758 TTCTCCTCTCTCATCCTTGCCTGTGGCTCTCCAAGCCTATGCATTATGTCCCATCTATACTGCAG TTCTCCTCTCTCATCCTTGCCTGTGGCTCTCCGAGCCTATGCATTATGTCCCATCTATACTGCAG A G lnc-BEX3-1 RNACentral:URS00008BC40A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:103309707..103309880 26863196 MeRIP-seq:(Medium) rs1303921347 Functional Loss SNV dbSNP153 33..33 33 - - - 69139 RMVar_ID_69139 Human_SNP_ID_726881886 m1A Human chrX - 103309967 103309967 103309967 TTTCTCTCTGTCTCCTAGGAGTAATGGAGTCCAAAGAGGAACGAGCGTTAAACAATCTCATCGTG TTTCTCTCTGTCTCCTAGGAGTAATGGAGTCCTAAGAGGAACGAGCGTTAAACAATCTCATCGTG T A BEX2 Ensembl:ENSG00000133134 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:103309639..103310011 26863196 MeRIP-seq:(Medium) rs778448293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1709409,Human_RBP_ID_5046258,Human_RBP_ID_9352278 Human_Splice_Rec_2225805,Human_Splice_Rec_2225809,Human_Splice_Rec_2225813,Human_Splice_Rec_2225817 69140 RMVar_ID_69140 Human_SNP_ID_726881887 m1A Human chrX - 103309967 103309967 103309967 TTTCTCTCTGTCTCCTAGGAGTAATGGAGTCCAAAGAGGAACGAGCGTTAAACAATCTCATCGTG TTTCTCTCTGTCTCCTAGGAGTAATGGAGTCCCAAGAGGAACGAGCGTTAAACAATCTCATCGTG T G BEX2 Ensembl:ENSG00000133134 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:103309639..103310011 26863196 MeRIP-seq:(Medium) rs778448293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1709409,Human_RBP_ID_5046258,Human_RBP_ID_9352278 Human_Splice_Rec_2225805,Human_Splice_Rec_2225809,Human_Splice_Rec_2225813,Human_Splice_Rec_2225817 69141 RMVar_ID_69141 Human_SNP_ID_726889636 m1A Human chrX + 103357732 103357732 103357732 AAAATGGAAGGAAAACCAGAAAATGAGAGTGAACCAAAGCATGAGGAAGAGCCAAAGCCTGAGGA AAAATGGAAGGAAAACCAGAAAATGAGAGTGAGCCAAAGCATGAGGAAGAGCCAAAGCCTGAGGA A G TCEAL9 Ensembl:ENSG00000185222 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:103356501..103357950;chrX:103356526..103357916 32194978 MeRIP-seq:(Medium) rs754749104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_724158,Human_RBP_ID_1709419,Human_RBP_ID_2068092,Human_RBP_ID_3234662,Human_RBP_ID_3912631,Human_RBP_ID_5637286,Human_RBP_ID_7962060,Human_RBP_ID_24319790,Human_RBP_ID_24549965,Human_RBP_ID_26363221,Human_RBP_ID_26772782,Human_RBP_ID_27834034 69142 RMVar_ID_69142 Human_SNP_ID_726893033 m1A Human chrX + 103377077 103377074 103377077 TCTCCGCGGCGCACCTCGCGGCGAGAATCCGGAGGAGAAGGAGACTGCAAGGATAGGCCCAGGTC TCTCCGCGGCGCACCTCGCGGCGAGAATCC___GGAGAAGGAGACTGCAAGGATAGGCCCAGGTC CGGA C BEX3 Ensembl:ENSG00000166681 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:103377026..103377125 26863196 MeRIP-seq:(Medium) rs962218092 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_257521,Human_RBP_ID_724188,Human_RBP_ID_1060229,Human_RBP_ID_1404444,Human_RBP_ID_1709435,Human_RBP_ID_2068102,Human_RBP_ID_5046324,Human_RBP_ID_5233359,Human_RBP_ID_7962083,Human_RBP_ID_8710345,Human_RBP_ID_16778867,Human_RBP_ID_18913235 Human_Splice_Rec_2225833,Human_Splice_Rec_2225834,Human_Splice_Rec_2225839,Human_Splice_Rec_2225840,Human_Splice_Rec_2225842 Human_miRNA_ID_2490984 RMVar_hsa_circ_99898,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369 69143 RMVar_ID_69143 Human_SNP_ID_726893042 m1A Human chrX - 103377098 103377098 103377098 CCCACCACCGTCCCTCGCACCGACCTGGGCCTATCCTTGCAGTCTCCTTCTCCTCCGGATTCTCG CCCACCACCGTCCCTCGCACCGACCTGGGCCTGTCCTTGCAGTCTCCTTCTCCTCCGGATTCTCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chrX:103376977..103377700;chrX:103377016..103377142 26863196 MeRIP-seq:(Medium) rs990627160 Functional Loss SNV dbSNP153 33..33 33 - - - 69144 RMVar_ID_69144 Human_SNP_ID_726893113 m1A Human chrX + 103377449 103377449 103377449 AAGCATTCAGTCTCTCTCCTTGCCTTTGTCTTACTTGTGTTCAAAGAAAAACAACCAGAAAAAAA AAGCATTCAGTCTCTCTCCTTGCCTTTGTCTTGCTTGTGTTCAAAGAAAAACAACCAGAAAAAAA A G BEX3 Ensembl:ENSG00000166681 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:103377445..103377852 26863196 MeRIP-seq:(Medium) rs887812131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3912643,Human_RBP_ID_22120295,Human_RBP_ID_23096937,Human_RBP_ID_26247228,Human_RBP_ID_27140968 RMVar_hsa_circ_99898,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369 69145 RMVar_ID_69145 Human_SNP_ID_726893120 m1A Human chrX + 103377475 103377474 103377475 TGTCTTACTTGTGTTCAAAGAAAAACAACCAGAAAAAAAAAATCTCATCATGGCAAATATTCACC TGTCTTACTTGTGTTCAAAGAAAAACAACCAG_AAAAAAAAATCTCATCATGGCAAATATTCACC GA G BEX3 Ensembl:ENSG00000166681 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs199898496 Functional Loss DEL dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8710347,Human_RBP_ID_27140969 Human_Splice_Rec_2225835,Human_Splice_Rec_2225837 RMVar_hsa_circ_99898,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369 69146 RMVar_ID_69146 Human_SNP_ID_726893122 m1A Human chrX + 103377475 103377475 103377475 TGTCTTACTTGTGTTCAAAGAAAAACAACCAGAAAAAAAAAATCTCATCATGGCAAATATTCACC TGTCTTACTTGTGTTCAAAGAAAAACAACCAGGAAAAAAAAATCTCATCATGGCAAATATTCACC A G BEX3 Ensembl:ENSG00000166681 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs765228803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8710347,Human_RBP_ID_27140969 Human_Splice_Rec_2225835,Human_Splice_Rec_2225837 RMVar_hsa_circ_99898,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369 69147 RMVar_ID_69147 Human_SNP_ID_726893159 m1A Human chrX + 103377594 103377594 103377594 TGGGAGGAGGTGAAGGCCACCAGCCTGCAGGAAATCGACGGGGACAGGCTCGCCGACTTGCCCCT TGGGAGGAGGTGAAGGCCACCAGCCTGCAGGAGATCGACGGGGACAGGCTCGCCGACTTGCCCCT A G BEX3 Ensembl:ENSG00000166681 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:103377551..103377725 26863196 MeRIP-seq:(Medium) rs375779393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257522,Human_RBP_ID_724193,Human_RBP_ID_5077448,Human_RBP_ID_9409423,Human_RBP_ID_17717313,Human_RBP_ID_22468019 Human_Splice_Rec_2225841,Human_Splice_Rec_2225843 Human_miRNA_ID_2225947,Human_miRNA_ID_2225948 RMVar_hsa_circ_99898,RMVar_hsa_circ_78978,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369,RMVar_hsa_circ_263370 69148 RMVar_ID_69148 Human_SNP_ID_726901869 m1A Human chrX - 103433451 103433451 103433451 GCCCAACAATTTCCTCTTAAAAAGGTGGCTCAAGTTAAAGGCACAGTCAAGGTTAATGCTCCTTT GCCCAACAATTTCCTCTTAAAAAGGTGGCTCAGGTTAAAGGCACAGTCAAGGTTAATGCTCCTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:103433448..103433811 26863196 MeRIP-seq:(Medium) rs780888974 Functional Loss SNV dbSNP153 33..33 33 - - - 69149 RMVar_ID_69149 Human_SNP_ID_726925758 m1A Human chrX - 103586109 103586109 103586109 CAGGCCCTTCTCATCCAACGTTTTCCTCCCCTACCTCCGCCGCACCCCAGCCGCCATTTCTTTCC CAGGCCCTTCTCATCCAACGTTTTCCTCCCCTCCCTCCGCCGCACCCCAGCCGCCATTTCTTTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:103586105..103586254 32194978 MeRIP-seq:(Medium) rs981108030 Functional Loss SNV dbSNP153 33..33 33 - - - 69150 RMVar_ID_69150 Human_SNP_ID_726929415 m1A Human chrX + 103609514 103609514 103609514 ATGAGAGAATGTGGAGATGTGTCAAGGGCTCAAGAGGAGCTAAGGAAAAAACAGAAAATGGGTGG ATGAGAGAATGTGGAGATGTGTCAAGGGCTCAGGAGGAGCTAAGGAAAAAACAGAAAATGGGTGG A G TCEAL3 Ensembl:ENSG00000196507 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:103609418..103609517 32194978 MeRIP-seq:(Medium) rs780244651 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1060241,Human_RBP_ID_24319988 69151 RMVar_ID_69151 Human_SNP_ID_726941783 m1A Human chrX + 103686628 103686628 103686628 TCATCGACCCTTTCTCCCCACCCCCACCCCGAAACCTGAAACGAGAATCCAGATCTTCCCAGCAG TCATCGACCCTTTCTCCCCACCCCCACCCCGACACCTGAAACGAGAATCCAGATCTTCCCAGCAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:103686626..103686700 26863410 MeRIP-seq:(Medium) rs1481945305 Functional Loss SNV dbSNP153 33..33 33 - - - 69152 RMVar_ID_69152 Human_SNP_ID_726941797 m1A Human chrX - 103686669 103686669 103686669 TTACTATGGCGGTTGGAGGAACGGCAGTGATCACACGTCGGCTGCTGGGAAGATCTGGATTCTCG TTACTATGGCGGTTGGAGGAACGGCAGTGATCGCACGTCGGCTGCTGGGAAGATCTGGATTCTCG T C MORF4L2 Ensembl:ENSG00000123562 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:103686553..103686700 26863196 MeRIP-seq:(Medium) rs1421088443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257948,Human_RBP_ID_724372,Human_RBP_ID_800289,Human_RBP_ID_1709580,Human_RBP_ID_5076683,Human_RBP_ID_5454975,Human_RBP_ID_5482808,Human_RBP_ID_5516939,Human_RBP_ID_7962589,Human_RBP_ID_8931675,Human_RBP_ID_9410072,Human_RBP_ID_16955871,Human_RBP_ID_18142925,Human_RBP_ID_18428015,Human_RBP_ID_18453923,Human_RBP_ID_19148553,Human_RBP_ID_22343165,Human_RBP_ID_23107387,Human_RBP_ID_23117417,Human_RBP_ID_24320163,Human_RBP_ID_27378061 Human_Splice_Rec_2225958,Human_Splice_Rec_2225963,Human_Splice_Rec_2225968,Human_Splice_Rec_2225994,Human_Splice_Rec_2226004,Human_Splice_Rec_2226015,Human_Splice_Rec_2226021 69153 RMVar_ID_69153 Human_SNP_ID_726941798 m1A Human chrX - 103686669 103686669 103686669 TTACTATGGCGGTTGGAGGAACGGCAGTGATCACACGTCGGCTGCTGGGAAGATCTGGATTCTCG TTACTATGGCGGTTGGAGGAACGGCAGTGATCCCACGTCGGCTGCTGGGAAGATCTGGATTCTCG T G MORF4L2 Ensembl:ENSG00000123562 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:103686553..103686700 26863196 MeRIP-seq:(Medium) rs1421088443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257948,Human_RBP_ID_724372,Human_RBP_ID_800289,Human_RBP_ID_1709580,Human_RBP_ID_5076683,Human_RBP_ID_5454975,Human_RBP_ID_5482808,Human_RBP_ID_5516939,Human_RBP_ID_7962589,Human_RBP_ID_8931675,Human_RBP_ID_9410072,Human_RBP_ID_16955871,Human_RBP_ID_18142925,Human_RBP_ID_18428015,Human_RBP_ID_18453923,Human_RBP_ID_19148553,Human_RBP_ID_22343165,Human_RBP_ID_23107387,Human_RBP_ID_23117417,Human_RBP_ID_24320163,Human_RBP_ID_27378061 Human_Splice_Rec_2225958,Human_Splice_Rec_2225963,Human_Splice_Rec_2225968,Human_Splice_Rec_2225994,Human_Splice_Rec_2226004,Human_Splice_Rec_2226015,Human_Splice_Rec_2226021 69154 RMVar_ID_69154 Human_SNP_ID_727017194 m1A Human chrX + 104134983 104134973 104134983 TTTCTGGGCTCATCTCCTGCCACTCCTCCATGATGCCCCAAAGCCCAGCCACACTGAATTACTCT TTTCTGGGCTCATCTCCTGCCAC__________TGCCCCAAAGCCCAGCCACACTGAATTACTCT CTCCTCCATGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:104134977..104135277 26863196 MeRIP-seq:(Medium) rs1230121135 Functional Loss DEL dbSNP153 24..33 33 - - - 69155 RMVar_ID_69155 Human_SNP_ID_727020801 m1A Human chrX - 104156964 104156964 104156964 TGCGTCGCTTAAGTGAGGGCGGCGGATGGGCGAAGGTCCGGTGACTGCGACTGTCGCTGCTTTCT TGCGTCGCTTAAGTGAGGGCGGCGGATGGGCGTAGGTCCGGTGACTGCGACTGTCGCTGCTTTCT T A SLC25A53 Ensembl:ENSG00000269743 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:104131222..104156977 26863196 MeRIP-seq:(Medium) rs1556371601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5046590 Human_Splice_Rec_2226615,Human_Splice_Rec_2226617 69156 RMVar_ID_69156 Human_SNP_ID_727027016 m1A Human chrX - 104194652 104194651 104194653 GCCTTTGACAATAGTCCTTAAATTCCCAACACAAAGGTTCAGAATAGATAATACTTGTTAAGTGA GCCTTTGACAATAGTCCTTAAATTCCCAACA__AAGGTTCAGAATAGATAATACTTGTTAAGTGA TTG T RF00017-8600 RNACentral:URS000099CE90 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:104194601..104194701 32194978 MeRIP-seq:(Medium) rs1251345388 Functional Loss DEL dbSNP153 32..33 33 - - - 69157 RMVar_ID_69157 Human_SNP_ID_635160296 m1A Human chr18 + 80909 80906 80910 AGACACATACACACACAGACACACACATAAACACACACACAGACATACACAAACACACACAGACA AGACACATACACACACAGACACACACATAA____ACACACAGACATACACAAACACACACAGACA AACAC A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:80895..81008 26863196 MeRIP-seq:(Medium) rs1297416179 Functional Loss DEL dbSNP153 31..34 33 - - - 69158 RMVar_ID_69158 Human_SNP_ID_635160297 m1A Human chr18 + 80909 80906 80910 AGACACATACACACACAGACACACACATAAACACACACACAGACATACACAAACACACACAGACA AGACACATACACACACAGACACACACATAAAC__ACACACAGACATACACAAACACACACAGACA AACAC AAC - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:80895..81008 26863196 MeRIP-seq:(Medium) rs1297416179 Functional Loss DEL dbSNP153 33..34 33 - - - 69159 RMVar_ID_69159 Human_SNP_ID_635187738 m1A Human chr18 + 158619 158619 158619 CACCACCGCGCCTCCGCCTCGGCCGCCGCCGCAGCTGCTCCTGGTCCCCGTCCCTTTGCCGCCCT CACCACCGCGCCTCCGCCTCGGCCGCCGCCGCTGCTGCTCCTGGTCCCCGTCCCTTTGCCGCCCT A T USP14 Ensembl:ENSG00000101557 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr18:158551..158745;chr18:158477..158758;chr18:158500..158757 26863196 MeRIP-seq:(Medium) rs938350774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768904,Human_RBP_ID_4483279,Human_RBP_ID_9327674,Human_RBP_ID_9379703,Human_RBP_ID_22533022 Human_Splice_Rec_1887253,Human_Splice_Rec_1887281,Human_Splice_Rec_1887309,Human_Splice_Rec_1887313,Human_Splice_Rec_1887343,Human_Splice_Rec_1887369 Human_miRNA_ID_2995049 RMVar_hsa_circ_188160,RMVar_hsa_circ_97993 69160 RMVar_ID_69160 Human_SNP_ID_635187752 m1A Human chr18 + 158662 158662 158662 GTCCCCGTCCCTTTGCCGCCCTCGTCAGGCCCAGCTCTCCTGCGCCGCCGCCTCCCGCCGCGCCC GTCCCCGTCCCTTTGCCGCCCTCGTCAGGCCCGGCTCTCCTGCGCCGCCGCCTCCCGCCGCGCCC A G USP14 Ensembl:ENSG00000101557 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:158592..158690 26863410 MeRIP-seq:(Medium) rs1213133833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768904,Human_RBP_ID_823356,Human_RBP_ID_906253,Human_RBP_ID_4483285,Human_RBP_ID_9327674,Human_RBP_ID_9379703,Human_RBP_ID_22533022 Human_Splice_Rec_1887253,Human_Splice_Rec_1887281,Human_Splice_Rec_1887309,Human_Splice_Rec_1887313,Human_Splice_Rec_1887343,Human_Splice_Rec_1887369 RMVar_hsa_circ_188160,RMVar_hsa_circ_97993 69161 RMVar_ID_69161 Human_SNP_ID_635187762 m1A Human chr18 - 158682 158673 158683 CGGAGTAGAGCGGCATGGCGGGGCGCGGCGGGAGGCGGCGGCGCAGGAGAGCTGGGCCTGACGAG CGGAGTAGAGCGGCATGGCGGGGCGCGGCGG__________CGCAGGAGAGCTGGGCCTGACGAG GCCGCCGCCTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:158511..158875 26863196 MeRIP-seq:(Medium) rs1391390880 Functional Loss DEL dbSNP153 32..41 33 - - - 69162 RMVar_ID_69162 Human_SNP_ID_635187768 m1A Human chr18 - 158682 158682 158682 CGGAGTAGAGCGGCATGGCGGGGCGCGGCGGGAGGCGGCGGCGCAGGAGAGCTGGGCCTGACGAG CGGAGTAGAGCGGCATGGCGGGGCGCGGCGGGGGGCGGCGGCGCAGGAGAGCTGGGCCTGACGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:158511..158875 26863196 MeRIP-seq:(Medium) rs768034681 Functional Loss SNV dbSNP153 33..33 33 - - - 69163 RMVar_ID_69163 Human_SNP_ID_635188960 m1A Human chr18 + 163357 163357 163357 AAGGAGAAATTTGAAGGTGTAGAATTGAATACAGATGAACCTCCAATGGTATTCAAGGCTCAGCT AAGGAGAAATTTGAAGGTGTAGAATTGAATACGGATGAACCTCCAATGGTATTCAAGGCTCAGCT A G USP14 Ensembl:ENSG00000101557 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr18:163262..163425;chr18:163246..163375 26863196 MeRIP-seq:(Medium) rs1447406722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_278935,Human_RBP_ID_1548173,Human_RBP_ID_1873028,Human_RBP_ID_4494079,Human_RBP_ID_8469011,Human_RBP_ID_13254841,Human_RBP_ID_18714543,Human_RBP_ID_22445994 Human_Splice_Rec_1887254,Human_Splice_Rec_1887255,Human_Splice_Rec_1887282,Human_Splice_Rec_1887283,Human_Splice_Rec_1887312,Human_Splice_Rec_1887314,Human_Splice_Rec_1887315,Human_Splice_Rec_1887344,Human_Splice_Rec_1887345,Human_Splice_Rec_1887370,Human_Splice_Rec_1887371,Human_Splice_Rec_1887398,Human_Splice_Rec_1887399 RMVar_hsa_circ_188161,RMVar_hsa_circ_71942,RMVar_hsa_circ_277376,RMVar_hsa_circ_188160,RMVar_hsa_circ_97993,RMVar_hsa_circ_331875,RMVar_hsa_circ_348058,RMVar_hsa_circ_355027,RMVar_hsa_circ_326915,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_73117,RMVar_hsa_circ_188163,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_188162 69164 RMVar_ID_69164 Human_SNP_ID_635188962 m1A Human chr18 - 163360 163360 163360 AACAGCTGAGCCTTGAATACCATTGGAGGTTCATCTGTATTCAATTCTACACCTTCAAATTTCTC AACAGCTGAGCCTTGAATACCATTGGAGGTTCGTCTGTATTCAATTCTACACCTTCAAATTTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:163245..163450 26863196 MeRIP-seq:(Medium) rs749060033 Functional Loss SNV dbSNP153 33..33 33 - - - 69165 RMVar_ID_69165 Human_SNP_ID_635202190 m1A Human chr18 + 214680 214680 214680 TTAGTTAGACTTTCTGCAAGGTCACTTAATCCAGACTTATTCAGTGCATTAATCAGATTCTCAGG TTAGTTAGACTTTCTGCAAGGTCACTTAATCCTGACTTATTCAGTGCATTAATCAGATTCTCAGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:214629..214709 32194978 MeRIP-seq:(Medium) rs1461668114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2536402,Human_RBP_ID_3552156 69166 RMVar_ID_69166 Human_SNP_ID_635213680 m1A Human chr18 - 263434 263434 263434 GAGGAGAGGACAATGAGAATGATGAGGAAAGAAGCAGGTTAGGTCCATTTATAAAGGGCACTGGG GAGGAGAGGACAATGAGAATGATGAGGAAAGACGCAGGTTAGGTCCATTTATAAAGGGCACTGGG T G THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:263383..263538 26863196 MeRIP-seq:(Medium) rs556954322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9906757,Human_RBP_ID_13277549 RMVar_hsa_circ_22291,RMVar_hsa_circ_64017 69167 RMVar_ID_69167 Human_SNP_ID_635214872 m1A Human chr18 - 267995 267995 267995 CCGAGAAGATGTCTCCGACGCCGCCGCTCTTCAGTTTGCCCGAAGCGCGGACGCGGTTTACGGTG CCGAGAAGATGTCTCCGACGCCGCCGCTCTTCTGTTTGCCCGAAGCGCGGACGCGGTTTACGGTG T A THOC1 Ensembl:ENSG00000079134 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:267929..267994 26863196 MeRIP-seq:(Medium) rs779066227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823113,Human_RBP_ID_4494080,Human_RBP_ID_9379455,Human_RBP_ID_18420637,Human_RBP_ID_26334517,Human_RBP_ID_27814452 Human_Splice_Rec_1887427,Human_Splice_Rec_1887463,Human_Splice_Rec_1887549,Human_Splice_Rec_1887599,Human_Splice_Rec_1887635,Human_Splice_Rec_1887717,Human_Splice_Rec_1887743,Human_Splice_Rec_1887755,Human_Splice_Rec_1887771,Human_Splice_Rec_1887777,Human_Splice_Rec_1887781 RMVar_hsa_circ_13118 69168 RMVar_ID_69168 Human_SNP_ID_635214873 m1A Human chr18 - 267995 267995 267995 CCGAGAAGATGTCTCCGACGCCGCCGCTCTTCAGTTTGCCCGAAGCGCGGACGCGGTTTACGGTG CCGAGAAGATGTCTCCGACGCCGCCGCTCTTCCGTTTGCCCGAAGCGCGGACGCGGTTTACGGTG T G THOC1 Ensembl:ENSG00000079134 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:267929..267994 26863196 MeRIP-seq:(Medium) rs779066227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823113,Human_RBP_ID_4494080,Human_RBP_ID_9379455,Human_RBP_ID_18420637,Human_RBP_ID_26334517,Human_RBP_ID_27814452 Human_Splice_Rec_1887427,Human_Splice_Rec_1887463,Human_Splice_Rec_1887549,Human_Splice_Rec_1887599,Human_Splice_Rec_1887635,Human_Splice_Rec_1887717,Human_Splice_Rec_1887743,Human_Splice_Rec_1887755,Human_Splice_Rec_1887771,Human_Splice_Rec_1887777,Human_Splice_Rec_1887781 RMVar_hsa_circ_13118 69169 RMVar_ID_69169 Human_SNP_ID_635214979 m1A Human chr18 - 268186 268186 268186 CGAGTAGGCTGTTTGGCTGACTCAGGCGCCCAACGCCCACCCGAACTGAGTCGCTAGGGAAACTC CGAGTAGGCTGTTTGGCTGACTCAGGCGCCCAGCGCCCACCCGAACTGAGTCGCTAGGGAAACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:268143..268260 26863196 MeRIP-seq:(Medium) rs939564218 Functional Loss SNV dbSNP153 33..33 33 - - - 69170 RMVar_ID_69170 Human_SNP_ID_635227935 m1A Human chr18 - 319935 319935 319935 CTCATCAGATTGAAAAAAAAAAAGCACTGAAAACCAATTACTGAAAAAAAATTGACAGCTAGTGT CTCATCAGATTGAAAAAAAAAAAGCACTGAAAGCCAATTACTGAAAAAAAATTGACAGCTAGTGT T C COLEC12 Ensembl:ENSG00000158270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9079916 69171 RMVar_ID_69171 Human_SNP_ID_635271115 m1A Human chr18 - 500673 500665 500674 AGGCAGCAGAGCGCGGAGCCGGGAGCGCGGGGAGCGCGGGCCGGCGGCGGCGAGGGAGGACGGGG AGGCAGCAGAGCGCGGAGCCGGGAGCGCGGG_________CCGGCGGCGGCGAGGGAGGACGGGG GCCCGCGCTC G COLEC12 Ensembl:ENSG00000158270 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr18:500571..500672 26863410 MeRIP-seq:(Medium) rs565478954 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_4489164 69172 RMVar_ID_69172 Human_SNP_ID_635313063 m1A Human chr18 - 657817 657814 657818 TGCCCCAGGTACTGCAGCTCCCCGTGCGGCGGACGCGGCTCGGCGTCCCGCTCCTGTGCGGCGGG TGCCCCAGGTACTGCAGCTCCCCGTGCGGCG____CGGCTCGGCGTCCCGCTCCTGTGCGGCGGG GCGTC G TYMSOS Ensembl:ENSG00000176912 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:657626..657875 26863196 MeRIP-seq:(Medium) rs1482159340 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_906061 RMVar_hsa_circ_122571,RMVar_hsa_circ_188189 69173 RMVar_ID_69173 Human_SNP_ID_635313102 m1A Human chr18 + 657923 657923 657923 GCACGGGCACCGGCACCCTGTCGGTATTCGGCATGCAGGCGCGCTACAGCCTGAGAGGTGACGCC GCACGGGCACCGGCACCCTGTCGGTATTCGGCCTGCAGGCGCGCTACAGCCTGAGAGGTGACGCC A C TYMS Ensembl:ENSG00000176890 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:657901..657925 26863196 MeRIP-seq:(Medium) rs1013467217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238824,Human_RBP_ID_510505,Human_RBP_ID_1012400,Human_RBP_ID_4494084,Human_RBP_ID_6701728,Human_RBP_ID_8828729,Human_RBP_ID_9290830,Human_RBP_ID_17911989 Human_Splice_Rec_1887963,Human_Splice_Rec_1887975,Human_Splice_Rec_1887981,Human_Splice_Rec_1887989 69174 RMVar_ID_69174 Human_SNP_ID_635314264 m1A Human chr18 + 662247 662247 662247 TTTTTGGACAGCCTGGGATTCTCCACCAGAGAAGAAGGGGACTTGGGCCCAGTTTATGGCTTCCA TTTTTGGACAGCCTGGGATTCTCCACCAGAGAGGAAGGGGACTTGGGCCCAGTTTATGGCTTCCA A G TYMS Ensembl:ENSG00000176890 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:662198..662371 26863196 MeRIP-seq:(Medium) rs3786362 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_52161,Human_RBP_ID_510512,Human_RBP_ID_905563,Human_RBP_ID_1551463,Human_RBP_ID_1877701,Human_RBP_ID_4491300,Human_RBP_ID_5144539,Human_RBP_ID_6701760,Human_RBP_ID_13330952,Human_RBP_ID_18719296,Human_RBP_ID_18993252,Human_RBP_ID_22445846,Human_RBP_ID_23776195,Human_RBP_ID_26769652 Human_Splice_Rec_1887967,Human_Splice_Rec_1887979,Human_Splice_Rec_1887993 Human_miRNA_ID_3118844 RMVar_hsa_circ_12080,RMVar_hsa_circ_188190,RMVar_hsa_circ_319629,RMVar_hsa_circ_361301,RMVar_hsa_circ_188191,RMVar_hsa_circ_280930,RMVar_hsa_circ_288395,RMVar_hsa_circ_25599,RMVar_hsa_circ_188192 69175 RMVar_ID_69175 Human_SNP_ID_635316492 m1A Human chr18 - 667577 667510 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_________________________________ GTGATGGTGATGGTGATGGAGATGGTGATGGTGATGGTGATGGAGATGGTGATGGTGATGGAGATGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990841 Functional Loss DEL dbSNP153 33..65 33 - - - 69176 RMVar_ID_69176 Human_SNP_ID_635316507 m1A Human chr18 - 667577 667522 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_________________________________ GTGATGGAGATGGTGATGGTGATGGTGATGGAGATGGTGATGGTGATGGAGATGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990870 Functional Loss DEL dbSNP153 33..65 33 - - - 69177 RMVar_ID_69177 Human_SNP_ID_635316513 m1A Human chr18 - 667577 667529 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_________________________________ AGATGGTGATGGTGATGGTGATGGAGATGGTGATGGTGATGGAGATGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990891 Functional Loss DEL dbSNP153 33..65 33 - - - 69178 RMVar_ID_69178 Human_SNP_ID_635316529 m1A Human chr18 - 667577 667540 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_________________________________ GTGATGGTGATGGAGATGGTGATGGTGATGGAGATGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990910 Functional Loss DEL dbSNP153 33..65 33 - - - 69179 RMVar_ID_69179 Human_SNP_ID_635316541 m1A Human chr18 - 667577 667549 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC____________________________TCACC ATGGAGATGGTGATGGTGATGGAGATGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1193597034 Functional Loss DEL dbSNP153 33..60 33 - - - 69180 RMVar_ID_69180 Human_SNP_ID_635316546 m1A Human chr18 - 667577 667552 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_________________________CCATCACC GAGATGGTGATGGTGATGGAGATGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990939 Functional Loss DEL dbSNP153 33..57 33 - - - 69181 RMVar_ID_69181 Human_SNP_ID_635316553 m1A Human chr18 - 667577 667553 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC________________________TCCATCACC AGATGGTGATGGTGATGGAGATGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1567990945 Functional Loss DEL dbSNP153 33..56 33 - - - 69182 RMVar_ID_69182 Human_SNP_ID_635316568 m1A Human chr18 - 667577 667564 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_____________CCATCACCATCTCCATCACC GTGATGGAGATGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1399796977 Functional Loss DEL dbSNP153 33..45 33 - - - 69183 RMVar_ID_69183 Human_SNP_ID_635316590 m1A Human chr18 - 667577 667575 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC__CATCTCCATCACCATCACCATCTCCATCACC GGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1371712692 Functional Loss DEL dbSNP153 33..34 33 - - - 69184 RMVar_ID_69184 Human_SNP_ID_635316592 m1A Human chr18 - 667577 667576 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATC_CCATCTCCATCACCATCACCATCTCCATCACC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs1393615863 Functional Loss DEL dbSNP153 33..33 33 - - - 69185 RMVar_ID_69185 Human_SNP_ID_635316594 m1A Human chr18 - 667577 667577 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATCTCCATCTCCATCACCATCACCATCTCCATCACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs371737383 Functional Loss SNV dbSNP153 33..33 33 - - - 69186 RMVar_ID_69186 Human_SNP_ID_635316595 m1A Human chr18 - 667577 667577 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATCGCCATCTCCATCACCATCACCATCTCCATCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs371737383 Functional Loss SNV dbSNP153 33..33 33 - - - 69187 RMVar_ID_69187 Human_SNP_ID_635323741 m1A Human chr18 - 691356 691356 691356 GGGCAACAGAGTGAGACCTTGTCTCTAAAAAAAGAATAATAAATTTTAAAAAACAAAATATAACC GGGCAACAGAGTGAGACCTTGTCTCTAAAAAAGGAATAATAAATTTTAAAAAACAAAATATAACC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:691352..691453 26863196 MeRIP-seq:(Medium) rs769904493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3559312,Human_RBP_ID_9904343,Human_RBP_ID_22965213,Human_RBP_ID_25379590 RMVar_hsa_circ_46684,RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199,RMVar_hsa_circ_301202,RMVar_hsa_circ_357752,RMVar_hsa_circ_54974,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_358512,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203 69188 RMVar_ID_69188 Human_SNP_ID_635328776 m1A Human chr18 + 708664 708664 708664 CTTGAAGAGGGAGAGCGCTTTATGATGAAGACAGAATGTGAGCTGGCCGGTCAAGGAAGGGGAGC CTTGAAGAGGGAGAGCGCTTTATGATGAAGACGGAATGTGAGCTGGCCGGTCAAGGAAGGGGAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:708628..708760 26863196 MeRIP-seq:(Medium) rs1164032301 Functional Loss SNV dbSNP153 33..33 33 - - - 69189 RMVar_ID_69189 Human_SNP_ID_635328964 m1A Human chr18 + 709379 709379 709379 CCACGAGGGGAGAGAGCACACGAAGAAGAGGCAGCCGACAGCGGAAAACGTATCTGAGGGTAAGG CCACGAGGGGAGAGAGCACACGAAGAAGAGGCGGCCGACAGCGGAAAACGTATCTGAGGGTAAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:709376..709400 26863196 MeRIP-seq:(Medium) rs2847330 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8268,GWAS_ID_8269,GWAS_ID_8270,GWAS_ID_8271,GWAS_ID_8272,GWAS_ID_8273,GWAS_ID_8274,GWAS_ID_8275,GWAS_ID_8276,GWAS_ID_8277,GWAS_ID_8278,GWAS_ID_8279,GWAS_ID_8280,GWAS_ID_8281,GWAS_ID_8282,GWAS_ID_8283,GWAS_ID_8284,GWAS_ID_8285,GWAS_ID_8286,GWAS_ID_8287,GWAS_ID_8288,GWAS_ID_8289,GWAS_ID_8290,GWAS_ID_8291,GWAS_ID_8292,GWAS_ID_8293,GWAS_ID_8294,GWAS_ID_8295,GWAS_ID_8296,GWAS_ID_8297,GWAS_ID_8298,GWAS_ID_8299,GWAS_ID_8300,GWAS_ID_8301,GWAS_ID_8302,GWAS_ID_8303,GWAS_ID_8304 69190 RMVar_ID_69190 Human_SNP_ID_635329999 m1A Human chr18 + 712586 712586 712586 GGACCGAGAGCCGGGAGATCCTGCCGCGCACCATGGCCCCTGCGCCCCGTGGCCGCGGCCCCCGT GGACCGAGAGCCGGGAGATCCTGCCGCGCACCCTGGCCCCTGCGCCCCGTGGCCGCGGCCCCCGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:712500..712587 26863196 MeRIP-seq:(Medium) rs1326173506 Functional Loss SNV dbSNP153 33..33 33 - - - 69191 RMVar_ID_69191 Human_SNP_ID_635342340 m1A Human chr18 + 756774 756774 756774 ACACTTGTACTGACAGGCTCTGGAGTATTTTCAGGTCTGTATTTAATGGCTGGACTTTTGTTTTC ACACTTGTACTGACAGGCTCTGGAGTATTTTCCGGTCTGTATTTAATGGCTGGACTTTTGTTTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:756725..775081 26863196 MeRIP-seq:(Medium) rs775990971 Functional Loss SNV dbSNP153 33..33 33 - - - 69192 RMVar_ID_69192 Human_SNP_ID_635357027 m1A Human chr18 - 812140 812140 812140 GCCCTCCGCCACCTCGAGCTGCGGTAGCAGCGACTCATGAGAGCGCGGCCGGAGGACAGGTAAGG GCCCTCCGCCACCTCGAGCTGCGGTAGCAGCGCCTCATGAGAGCGCGGCCGGAGGACAGGTAAGG T G YES1 Ensembl:ENSG00000176105 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:812127..812211 26863196 MeRIP-seq:(Medium) rs1338605427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4493198,Human_RBP_ID_5238086,Human_RBP_ID_9083643,Human_RBP_ID_17913010 Human_Splice_Rec_1888363,Human_Splice_Rec_1888407,Human_Splice_Rec_1888413 69193 RMVar_ID_69193 Human_SNP_ID_635357059 m1A Human chr18 - 812215 812215 812215 CTGCCGTCGTTGCTGCCGCCGGGCGCCCCGGGACGAGGAGGTGGAGGAGGGAGAGGGCCCGCGGG CTGCCGTCGTTGCTGCCGCCGGGCGCCCCGGGGCGAGGAGGTGGAGGAGGGAGAGGGCCCGCGGG T C YES1 Ensembl:ENSG00000176105 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:812070..812270 26863196 MeRIP-seq:(Medium) rs1431778021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238822,Human_RBP_ID_4493914,Human_RBP_ID_9327678 69194 RMVar_ID_69194 Human_SNP_ID_635357203 m1A Human chr18 + 812421 812421 812421 CGCGCCGCCGTCCGCTCACCGGAACTCGGGCCACGCCGGCCCGGCTCCGGGGCCCCCAGCCTTCC CGCGCCGCCGTCCGCTCACCGGAACTCGGGCCGCGCCGGCCCGGCTCCGGGGCCCCCAGCCTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:812390..812535 26863196 MeRIP-seq:(Medium) rs7240974 Functional Loss SNV dbSNP153 33..33 33 - - - 69195 RMVar_ID_69195 Human_SNP_ID_635771597 m1A Human chr18 - 2538789 2538789 2538789 TTGAGTTGCACTAACATTCTATGTTATTCTAGACTATACAAATTAAGTGGTAAGCAGTTATAAAG TTGAGTTGCACTAACATTCTATGTTATTCTAGGCTATACAAATTAAGTGGTAAGCAGTTATAAAG T C METTL4 Ensembl:ENSG00000101574 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11663148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22390400 Human_miRNA_ID_1554126,Human_miRNA_ID_1556011,Human_miRNA_ID_1557793,Human_miRNA_ID_1570198,Human_miRNA_ID_1576580,Human_miRNA_ID_1583732,Human_miRNA_ID_1617703,Human_miRNA_ID_1662003,Human_miRNA_ID_1663223,Human_miRNA_ID_1682119 GWAS_ID_8305 69196 RMVar_ID_69196 Human_SNP_ID_635773925 m1A Human chr18 - 2548644 2548644 2548644 TGGTTTCAGAGAAGGAGCAAGTGTGAGTGATGACAGGGTCCAGGTTATGGCATTGGAGTGGATTA TGGTTTCAGAGAAGGAGCAAGTGTGAGTGATGTCAGGGTCCAGGTTATGGCATTGGAGTGGATTA T A METTL4 Ensembl:ENSG00000101574 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:2548576..2548660 26863196 MeRIP-seq:(Medium) rs1275541382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188224,RMVar_hsa_circ_116581,RMVar_hsa_circ_314541,RMVar_hsa_circ_188225,RMVar_hsa_circ_831,RMVar_hsa_circ_310842,RMVar_hsa_circ_307508,RMVar_hsa_circ_366807,RMVar_hsa_circ_304291,RMVar_hsa_circ_188226 69197 RMVar_ID_69197 Human_SNP_ID_635779569 m1A Human chr18 - 2571862 2571861 2571862 CTTTCCTCCTTGGGAAATCGTTGCCACTAGAAATTTAATAGATCCCGTGAAACCAGCGCCTCGCA CTTTCCTCCTTGGGAAATCGTTGCCACTAGAA_TTTAATAGATCCCGTGAAACCAGCGCCTCGCA AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:2571856..2572146 26863196 MeRIP-seq:(Medium) rs1270974298 Functional Loss DEL dbSNP153 33..33 33 - - - 69198 RMVar_ID_69198 Human_SNP_ID_635801375 m1A Human chr18 - 2655995 2655995 2655995 GGGCTGAGGTGCGCGCTCCGCGCGGCGCCTTCAGCTCCAGCTCCCGGGGCGGCTCGAGGCCTCGG GGGCTGAGGTGCGCGCTCCGCGCGGCGCCTTCTGCTCCAGCTCCCGGGGCGGCTCGAGGCCTCGG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:2655951..2656150 26863196 MeRIP-seq:(Medium) rs559165250 Functional Loss SNV dbSNP153 33..33 33 - - - 69199 RMVar_ID_69199 Human_SNP_ID_635801383 m1A Human chr18 - 2656028 2656028 2656028 AAAAGACAGCGACGCCTGCCGCCGCCGGGCTCAGGGCTGAGGTGCGCGCTCCGCGCGGCGCCTTC AAAAGACAGCGACGCCTGCCGCCGCCGGGCTCTGGGCTGAGGTGCGCGCTCCGCGCGGCGCCTTC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:2655982..2656112 26863196 MeRIP-seq:(Medium) rs757001580 Functional Loss SNV dbSNP153 33..33 33 - - - 69200 RMVar_ID_69200 Human_SNP_ID_635801401 m1A Human chr18 - 2656065 2656065 2656065 CGCCGCCGTCCGCCGCTGCCATATTGGGGAAAAGGAGAAAAGACAGCGACGCCTGCCGCCGCCGG CGCCGCCGTCCGCCGCTGCCATATTGGGGAAATGGAGAAAAGACAGCGACGCCTGCCGCCGCCGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:2655755..2656137 26863196 MeRIP-seq:(Medium) rs769172056 Functional Loss SNV dbSNP153 33..33 33 - - - 69201 RMVar_ID_69201 Human_SNP_ID_635897554 m1A Human chr18 + 3013278 3013278 3013278 CTGGGCCGCAGCTGAGTCGGGCGGCCCTCATGAATGGGACGCCGCGGCTGCGGCGGCCGAGCCGG CTGGGCCGCAGCTGAGTCGGGCGGCCCTCATGGATGGGACGCCGCGGCTGCGGCGGCCGAGCCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:3013189..3013309 26863410 MeRIP-seq:(Medium) rs909811407 Functional Loss SNV dbSNP153 33..33 33 - - - 69202 RMVar_ID_69202 Human_SNP_ID_635956658 m1A Human chr18 - 3247858 3247858 3247858 CCGAGCACCTCTCCGAGCCCCTCGCTGCCGCTATCACACCACCCTGCTACCCAGAGAGCCGCTAA CCGAGCACCTCTCCGAGCCCCTCGCTGCCGCTTTCACACCACCCTGCTACCCAGAGAGCCGCTAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr18:3247801..3248025;chr18:3247801..3248011;chr18:3247801..3247963 26863196 MeRIP-seq:(Medium) rs1020617883 Functional Loss SNV dbSNP153 33..33 33 - - - 69203 RMVar_ID_69203 Human_SNP_ID_635956659 m1A Human chr18 - 3247858 3247858 3247858 CCGAGCACCTCTCCGAGCCCCTCGCTGCCGCTATCACACCACCCTGCTACCCAGAGAGCCGCTAA CCGAGCACCTCTCCGAGCCCCTCGCTGCCGCTGTCACACCACCCTGCTACCCAGAGAGCCGCTAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr18:3247801..3248025;chr18:3247801..3248011;chr18:3247801..3247963 26863196 MeRIP-seq:(Medium) rs1020617883 Functional Loss SNV dbSNP153 33..33 33 - - - 69204 RMVar_ID_69204 Human_SNP_ID_635956667 m1A Human chr18 + 3247869 3247869 3247869 CTGGGTAGCAGGGTGGTGTGATAGCGGCAGCGAGGGGCTCGGAGAGGTGCTCGGATTCTCGTAGC CTGGGTAGCAGGGTGGTGTGATAGCGGCAGCGTGGGGCTCGGAGAGGTGCTCGGATTCTCGTAGC A T MYL12A Ensembl:ENSG00000101608 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:3247776..3247980 26863196 MeRIP-seq:(Medium) rs1446512402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51363,Human_RBP_ID_238535,Human_RBP_ID_507297,Human_RBP_ID_768940,Human_RBP_ID_823178,Human_RBP_ID_906692,Human_RBP_ID_4486297,Human_RBP_ID_5319574,Human_RBP_ID_5468113,Human_RBP_ID_6681753,Human_RBP_ID_9327685,Human_RBP_ID_17693868,Human_RBP_ID_17913398,Human_RBP_ID_18420782,Human_RBP_ID_18440118,Human_RBP_ID_22445851,Human_RBP_ID_23767130 Human_Splice_Rec_1890027,Human_Splice_Rec_1890033,Human_Splice_Rec_1890035,Human_Splice_Rec_1890043,Human_Splice_Rec_1890045 Human_miRNA_ID_2937691 RMVar_hsa_circ_111475,RMVar_hsa_circ_188309 69205 RMVar_ID_69205 Human_SNP_ID_635958124 m1A Human chr18 + 3253234 3253234 3253234 TGGTTTTTATTGTATTTCCTTTCCTAATTAGGACTTAACCACCACCATGTCGAGCAAAAGAACAA TGGTTTTTATTGTATTTCCTTTCCTAATTAGGCCTTAACCACCACCATGTCGAGCAAAAGAACAA A C MYL12A Ensembl:ENSG00000101608 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:3253226..3253350 32194978 MeRIP-seq:(Medium) rs1418882490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51364,Human_RBP_ID_906146,Human_RBP_ID_4486303,Human_RBP_ID_9379744,Human_RBP_ID_22226518,Human_RBP_ID_22445852,Human_RBP_ID_26334537,Human_RBP_ID_26978635,Human_RBP_ID_27561712 Human_Splice_Rec_1890022,Human_Splice_Rec_1890028,Human_Splice_Rec_1890034,Human_Splice_Rec_1890038,Human_Splice_Rec_1890050,Human_Splice_Rec_1890052,Human_Splice_Rec_1890056,Human_Splice_Rec_1890058,Human_Splice_Rec_1890064 RMVar_hsa_circ_126747,RMVar_hsa_circ_111475,RMVar_hsa_circ_188309,RMVar_hsa_circ_69999,RMVar_hsa_circ_188310,RMVar_hsa_circ_355024 69206 RMVar_ID_69206 Human_SNP_ID_635958144 m1A Human chr18 + 3253282 3253282 3253282 GTCGAGCAAAAGAACAAAGACCAAGACCAAGAAGCGCCCTCAGCGTGCAACATCCAATGTGTTTG GTCGAGCAAAAGAACAAAGACCAAGACCAAGATGCGCCCTCAGCGTGCAACATCCAATGTGTTTG A T MYL12A Ensembl:ENSG00000101608 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr18:3253148..3253375;chr18:3253156..3253300;chr18:3253197..3253375;chr18:3253176..3253375;chr18:3253185..3253375;chr18:3253152..3253325 26863196 MeRIP-seq:(Medium) rs1427227249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494103,Human_RBP_ID_9379744,Human_RBP_ID_13290447,Human_RBP_ID_26334289 Human_Splice_Rec_1890022,Human_Splice_Rec_1890028,Human_Splice_Rec_1890034,Human_Splice_Rec_1890038,Human_Splice_Rec_1890050,Human_Splice_Rec_1890052,Human_Splice_Rec_1890056,Human_Splice_Rec_1890058,Human_Splice_Rec_1890064 RMVar_hsa_circ_126747,RMVar_hsa_circ_111475,RMVar_hsa_circ_188309,RMVar_hsa_circ_69999,RMVar_hsa_circ_188310,RMVar_hsa_circ_355024 69207 RMVar_ID_69207 Human_SNP_ID_635958815 m1A Human chr18 + 3256114 3256114 3256114 CTATTAATATCATTTTCAGAATAAAAAATAGGATAATTTAACCTACCAGCCCTTCTCCCCCAATA CTATTAATATCATTTTCAGAATAAAAAATAGGGTAATTTAACCTACCAGCCCTTCTCCCCCAATA A G MYL12A Ensembl:ENSG00000101608 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_507303,Human_RBP_ID_1370915,Human_RBP_ID_6681787,Human_RBP_ID_17265030,Human_RBP_ID_17381577,Human_RBP_ID_17496148,Human_RBP_ID_17655238,Human_RBP_ID_17908838,Human_RBP_ID_18298969,Human_RBP_ID_22390441,Human_RBP_ID_24417777,Human_RBP_ID_24483257,Human_RBP_ID_26978640,Human_RBP_ID_27461070 Human_miRNA_ID_966995 GWAS_ID_8306,GWAS_ID_8307,GWAS_ID_8308,GWAS_ID_8309,GWAS_ID_8310,GWAS_ID_8311,GWAS_ID_8312,GWAS_ID_8313,GWAS_ID_8314,GWAS_ID_8315,GWAS_ID_8316,GWAS_ID_8317,GWAS_ID_8318,GWAS_ID_8319,GWAS_ID_8320,GWAS_ID_8321,GWAS_ID_8322,GWAS_ID_8323,GWAS_ID_8324,GWAS_ID_8325,GWAS_ID_8326,GWAS_ID_8327,GWAS_ID_8328,GWAS_ID_8329,GWAS_ID_8330,GWAS_ID_8331,GWAS_ID_8332 RMVar_hsa_circ_126747,RMVar_hsa_circ_111475,RMVar_hsa_circ_188309,RMVar_hsa_circ_188310,RMVar_hsa_circ_188311 69208 RMVar_ID_69208 Human_SNP_ID_635960151 m1A Human chr18 + 3261901 3261900 3261901 CAAAGGAGCGGGGGACGAGGGCCGGGCTGCGGACGACCGCCGCAGCGCAGGCCGCGATATCGCAG CAAAGGAGCGGGGGACGAGGGCCGGGCTGCGG_CGACCGCCGCAGCGCAGGCCGCGATATCGCAG GA G MYL12B Ensembl:ENSG00000118680 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:3261887..3262032 26863196 MeRIP-seq:(Medium) rs940139956 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_188311 69209 RMVar_ID_69209 Human_SNP_ID_635960152 m1A Human chr18 + 3261901 3261901 3261901 CAAAGGAGCGGGGGACGAGGGCCGGGCTGCGGACGACCGCCGCAGCGCAGGCCGCGATATCGCAG CAAAGGAGCGGGGGACGAGGGCCGGGCTGCGGGCGACCGCCGCAGCGCAGGCCGCGATATCGCAG A G MYL12B Ensembl:ENSG00000118680 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:3261887..3262032 26863196 MeRIP-seq:(Medium) rs1579764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188311 69210 RMVar_ID_69210 Human_SNP_ID_635960301 m1A Human chr18 - 3262195 3262195 3262195 ACACCAGAACCGGGGCCGCCCTGCGCGAGACCACAAACGACAGCGAAGAGCGTTAGGCTGTGGCC ACACCAGAACCGGGGCCGCCCTGCGCGAGACCGCAAACGACAGCGAAGAGCGTTAGGCTGTGGCC T C LOC104968399 RNACentral:URS00007E440A lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:3262126..3262200 26863196 MeRIP-seq:(Medium) rs11650 Functional Loss SNV dbSNP153 33..33 33 - - - 69211 RMVar_ID_69211 Human_SNP_ID_635962018 m1A Human chr18 - 3269045 3269045 3269045 AAACTGCAAATGTCCCCAAGGTACCATGCCACATCTTATCTTGTATATCTTTGTTCCTGCTATTT AAACTGCAAATGTCCCCAAGGTACCATGCCACCTCTTATCTTGTATATCTTTGTTCCTGCTATTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:3269041..3269371 26863196 MeRIP-seq:(Medium) rs1485990962 Functional Loss SNV dbSNP153 33..33 33 - - - 69212 RMVar_ID_69212 Human_SNP_ID_635962019 m1A Human chr18 + 3269051 3269051 3269051 CAGGAACAAAGATATACAAGATAAGATGTGGCATGGTACCTTGGGGACATTTGCAGTTTGGTGTT CAGGAACAAAGATATACAAGATAAGATGTGGCGTGGTACCTTGGGGACATTTGCAGTTTGGTGTT A G MYL12B Ensembl:ENSG00000118680 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:3269047..3269400 26863196 MeRIP-seq:(Medium) rs1186952694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6681873,Human_RBP_ID_13290619 RMVar_hsa_circ_188311 69213 RMVar_ID_69213 Human_SNP_ID_635962919 m1A Human chr18 + 3272933 3272933 3272933 GTCGAGCAAAAAGGCAAAGACCAAGACCACCAAGAAGCGCCCTCAGCGTGCAACATCCAATGTGT GTCGAGCAAAAAGGCAAAGACCAAGACCACCAGGAAGCGCCCTCAGCGTGCAACATCCAATGTGT A G MYL12B Ensembl:ENSG00000118680 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:3272842..3272993 26863196 MeRIP-seq:(Medium) rs747544799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769220,Human_RBP_ID_4494107,Human_RBP_ID_18191497,Human_RBP_ID_22446009,Human_RBP_ID_26814258 Human_Splice_Rec_1890080,Human_Splice_Rec_1890086,Human_Splice_Rec_1890096,Human_Splice_Rec_1890102 RMVar_hsa_circ_29874,RMVar_hsa_circ_188311,RMVar_hsa_circ_319179 69214 RMVar_ID_69214 Human_SNP_ID_636007748 m1A Human chr18 + 3449770 3449770 3449770 GCCAGTAGAGTTCGGGGCAGCTGTCAAAAACGAGACGGGGAGGCTTTTCTTCCCGGGGGTGGAGG GCCAGTAGAGTTCGGGGCAGCTGTCAAAAACGCGACGGGGAGGCTTTTCTTCCCGGGGGTGGAGG A C TGIF1 Ensembl:ENSG00000177426 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:3449722..3450042 26863196 MeRIP-seq:(Medium) rs1326655414 Functional Loss SNV dbSNP153 33..33 33 - - - 69215 RMVar_ID_69215 Human_SNP_ID_636007916 m1A Human chr18 + 3450235 3450235 3450235 AGCAGGGAACAAAGGAGCGGAGAGGGGAGGGGAGAGAGTTGGGCGAGGGAGAGCCCCCGGCCGGC AGCAGGGAACAAAGGAGCGGAGAGGGGAGGGGTGAGAGTTGGGCGAGGGAGAGCCCCCGGCCGGC A T TGIF1 Ensembl:ENSG00000177426 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:3450176..3450526;chr18:3450166..3450531 26863196 MeRIP-seq:(Medium) rs1167515319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52383,Human_RBP_ID_769319,Human_RBP_ID_3561086,Human_RBP_ID_4493921,Human_RBP_ID_8232745,Human_RBP_ID_17655132,Human_RBP_ID_18420643,Human_RBP_ID_22064493,Human_RBP_ID_22717819,Human_RBP_ID_22741260,Human_RBP_ID_24373695 69216 RMVar_ID_69216 Human_SNP_ID_636008660 m1A Human chr18 + 3452080 3452080 3452080 CGGCTCTGATTCCTTTCCATGGCCCGCCTCCCACCCCGGGAATCCCCAGTGCTCCTTTTCCACGG CGGCTCTGATTCCTTTCCATGGCCCGCCTCCCCCCCCGGGAATCCCCAGTGCTCCTTTTCCACGG A C TGIF1 Ensembl:ENSG00000177426 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:3452077..3452150 26863196 MeRIP-seq:(Medium) rs867525200 Functional Loss SNV dbSNP153 33..33 33 - - - 69217 RMVar_ID_69217 Human_SNP_ID_636046337 m1A Human chr18 + 3596662 3596662 3596662 GTCTGTCTGTTCCACGGATGTAACCACAGCACACGCGTGGCTCACGGTACTAGTGTGATAAATGC GTCTGTCTGTTCCACGGATGTAACCACAGCACTCGCGTGGCTCACGGTACTAGTGTGATAAATGC A T DLGAP1-AS1 Ensembl:ENSG00000177337 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:3596612..3596986 26863196 MeRIP-seq:(Medium) rs1269896637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906101 Human_Splice_Rec_1890602,Human_Splice_Rec_1890608,Human_Splice_Rec_1890616,Human_Splice_Rec_1890617,Human_Splice_Rec_1890620,Human_Splice_Rec_1890621 69218 RMVar_ID_69218 Human_SNP_ID_636054204 m1A Human chr18 - 3623895 3623895 3623895 GAATGCAGGCAGGAGGGGAAACGGGCATCCGCACGGGGACCGGCCACATCCTAAGGCTGGAGGCT GAATGCAGGCAGGAGGGGAAACGGGCATCCGCCCGGGGACCGGCCACATCCTAAGGCTGGAGGCT T G DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:3623845..3624016;chr18:3623853..3623955 26863196 MeRIP-seq:(Medium) rs944689803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8551,RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 69219 RMVar_ID_69219 Human_SNP_ID_636449406 m1A Human chr18 + 5238130 5238130 5238130 CCGAGCGGGGAGCAAGGCCTGCGGGGAGGCGCAGGATGGACGCGTTGGCTGTCATGATGTAGGAC CCGAGCGGGGAGCAAGGCCTGCGGGGAGGCGCCGGATGGACGCGTTGGCTGTCATGATGTAGGAC A C LINC00667 Ensembl:ENSG00000263753 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:5235886..5238421;chr18:5238076..5238318 26863196 MeRIP-seq:(Medium) rs1266748797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22965719 69220 RMVar_ID_69220 Human_SNP_ID_636449407 m1A Human chr18 + 5238130 5238130 5238130 CCGAGCGGGGAGCAAGGCCTGCGGGGAGGCGCAGGATGGACGCGTTGGCTGTCATGATGTAGGAC CCGAGCGGGGAGCAAGGCCTGCGGGGAGGCGCGGGATGGACGCGTTGGCTGTCATGATGTAGGAC A G LINC00667 Ensembl:ENSG00000263753 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:5235886..5238421;chr18:5238076..5238318 26863196 MeRIP-seq:(Medium) rs1266748797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22965719 69221 RMVar_ID_69221 Human_SNP_ID_636465510 m1A Human chr18 - 5295665 5295665 5295665 ACCAGCCAGCTCCAGGATGTGCGGCGGCCGCCAGCGGCGCGGCGCGGTGCGAGCGGGGACGGGCG ACCAGCCAGCTCCAGGATGTGCGGCGGCCGCCGGCGGCGCGGCGCGGTGCGAGCGGGGACGGGCG T C ZBTB14 Ensembl:ENSG00000198081 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:5295619..5295729 26863196 MeRIP-seq:(Medium) rs1304469738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1890961,Human_Splice_Rec_1890973,Human_Splice_Rec_1890983 69222 RMVar_ID_69222 Human_SNP_ID_636515364 m1A Human chr18 - 5489107 5489089 5489107 GGAGGCCGAGCCCCAGGAGGCGGCGGGGGCGCAGGGGCGCGCGGGGGCGCCCGTGCCGGAGCCGC GGAGGCCGAGCCCCAGGAGGCGGCGGGGGCGC__________________CCGTGCCGGAGCCGC GGCGCCCCCGCGCGCCCCT G EPB41L3 Ensembl:ENSG00000082397 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:5489057..5489133 26863196 MeRIP-seq:(Medium) rs755462998 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_4489697 Human_Splice_Rec_1891008,Human_Splice_Rec_1891048,Human_Splice_Rec_1891090,Human_Splice_Rec_1891172,Human_Splice_Rec_1891210,Human_Splice_Rec_1891252,Human_Splice_Rec_1891292,Human_Splice_Rec_1891438,Human_Splice_Rec_1891444,Human_Splice_Rec_1891448,Human_Splice_Rec_1891452,Human_Splice_Rec_1891458,Human_Splice_Rec_1891462,Human_Splice_Rec_1891470,Human_Splice_Rec_1891474,Human_Splice_Rec_1891484 RMVar_hsa_circ_15935,RMVar_hsa_circ_345863,RMVar_hsa_circ_93422,RMVar_hsa_circ_188342,RMVar_hsa_circ_27828,RMVar_hsa_circ_363187,RMVar_hsa_circ_16599,RMVar_hsa_circ_33278,RMVar_hsa_circ_67639,RMVar_hsa_circ_21804,RMVar_hsa_circ_37082,RMVar_hsa_circ_378626,RMVar_hsa_circ_307936,RMVar_hsa_circ_188350,RMVar_hsa_circ_188351 69223 RMVar_ID_69223 Human_SNP_ID_636678144 m1A Human chr18 - 6134756 6134756 6134756 TCAACACCAGCCTATGAAAGCAGCCAGGAGGGAGGCTGTACCCTGCAAAGCCACAGGGGTGGAGC TCAACACCAGCCTATGAAAGCAGCCAGGAGGGCGGCTGTACCCTGCAAAGCCACAGGGGTGGAGC T G L3MBTL4 Ensembl:ENSG00000154655 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:6134737..6134821 26863410 MeRIP-seq:(Medium) rs1449509427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188355,RMVar_hsa_circ_267062,RMVar_hsa_circ_29913,RMVar_hsa_circ_317784,RMVar_hsa_circ_351608,RMVar_hsa_circ_356513,RMVar_hsa_circ_47584,RMVar_hsa_circ_303997,RMVar_hsa_circ_188356,RMVar_hsa_circ_188357,RMVar_hsa_circ_188358,RMVar_hsa_circ_313122,RMVar_hsa_circ_332252,RMVar_hsa_circ_346063,RMVar_hsa_circ_328304,RMVar_hsa_circ_20345,RMVar_hsa_circ_289748,RMVar_hsa_circ_188359 69224 RMVar_ID_69224 Human_SNP_ID_636826423 m1A Human chr18 + 6729426 6729403 6729427 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACAC________________________AGGCGCACACACACACAGGCGTGCACACGTA CAGGCACAAACACAGGCGCACACAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs1370993165 Functional Loss DEL dbSNP153 11..34 33 - - - 69225 RMVar_ID_69225 Human_SNP_ID_636826434 m1A Human chr18 + 6729426 6729413 6729427 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAAC______________AGGCGCACACACACACAGGCGTGCACACGTA CACAGGCGCACACAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs1273409621 Functional Loss DEL dbSNP153 21..34 33 - - - 69226 RMVar_ID_69226 Human_SNP_ID_636826437 m1A Human chr18 + 6729426 6729416 6729427 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAACACA___________AGGCGCACACACACACAGGCGTGCACACGTA AGGCGCACACAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs752948889 Functional Loss DEL dbSNP153 24..34 33 - - - 69227 RMVar_ID_69227 Human_SNP_ID_636826442 m1A Human chr18 + 6729426 6729419 6729427 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAACACAGGC________AGGCGCACACACACACAGGCGTGCACACGTA CGCACACAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs540276002 Functional Loss DEL dbSNP153 27..34 33 - - - GWAS_ID_8333,GWAS_ID_8334,GWAS_ID_8335,GWAS_ID_8336,GWAS_ID_8337,GWAS_ID_8338,GWAS_ID_8339,GWAS_ID_8340,GWAS_ID_8341,GWAS_ID_8342,GWAS_ID_8343,GWAS_ID_8344,GWAS_ID_8345,GWAS_ID_8346,GWAS_ID_8347 69228 RMVar_ID_69228 Human_SNP_ID_636826450 m1A Human chr18 + 6729426 6729425 6729427 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAACACAGGCGCACAC__AGGCGCACACACACACAGGCGTGCACACGTA CAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs1229387962 Functional Loss DEL dbSNP153 33..34 33 - - - 69229 RMVar_ID_69229 Human_SNP_ID_636826451 m1A Human chr18 + 6729426 6729426 6729426 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAACACAGGCGCACACGTAGGCGCACACACACACAGGCGTGCACACGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) rs930691110 Functional Loss SNV dbSNP153 33..33 33 - - - 69230 RMVar_ID_69230 Human_SNP_ID_636848135 m1A Human chr18 + 6824805 6824805 6824805 CTCGCTGCCGAAGAATTAACAGGATGCTCTCCAATGAATCCCTCCATCCTCCTGCCTTCAGCCGT CTCGCTGCCGAAGAATTAACAGGATGCTCTCCGATGAATCCCTCCATCCTCCTGCCTTCAGCCGT A G ARHGAP28 Ensembl:ENSG00000088756 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6824709..6824805 26863196 MeRIP-seq:(Medium) rs201097037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4491566 Human_Splice_Rec_1892032,Human_Splice_Rec_1892068,Human_Splice_Rec_1892070,Human_Splice_Rec_1892071,Human_Splice_Rec_1892078,Human_Splice_Rec_1892082 RMVar_hsa_circ_51376,RMVar_hsa_circ_188380,RMVar_hsa_circ_288083,RMVar_hsa_circ_297343,RMVar_hsa_circ_188378,RMVar_hsa_circ_188379,RMVar_hsa_circ_362568,RMVar_hsa_circ_363465,RMVar_hsa_circ_366760,RMVar_hsa_circ_312429,RMVar_hsa_circ_287718,RMVar_hsa_circ_290476,RMVar_hsa_circ_66802,RMVar_hsa_circ_188382,RMVar_hsa_circ_188384,RMVar_hsa_circ_188386,RMVar_hsa_circ_47680,RMVar_hsa_circ_188385,RMVar_hsa_circ_188383,RMVar_hsa_circ_188381 69231 RMVar_ID_69231 Human_SNP_ID_636898911 m1A Human chr18 - 7019030 7019030 7019030 AGTGGAGAAGGATGTGCTGGGGAGTTAGCAGCAGAGTCCGCACGGTCCAGCTACGGGGTTGATGG AGTGGAGAAGGATGTGCTGGGGAGTTAGCAGCGGAGTCCGCACGGTCCAGCTACGGGGTTGATGG T C LAMA1 Ensembl:ENSG00000101680 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7019028..7019348 26863196 MeRIP-seq:(Medium) rs1202674706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79821,RMVar_hsa_circ_99906,RMVar_hsa_circ_97602,RMVar_hsa_circ_188399,RMVar_hsa_circ_188401,RMVar_hsa_circ_87091,RMVar_hsa_circ_188400,RMVar_hsa_circ_333865,RMVar_hsa_circ_28270,RMVar_hsa_circ_188402,RMVar_hsa_circ_119733,RMVar_hsa_circ_7723,RMVar_hsa_circ_188404,RMVar_hsa_circ_126989,RMVar_hsa_circ_118131,RMVar_hsa_circ_188407,RMVar_hsa_circ_188408,RMVar_hsa_circ_376070,RMVar_hsa_circ_369856,RMVar_hsa_circ_110749,RMVar_hsa_circ_116237,RMVar_hsa_circ_188410,RMVar_hsa_circ_28802,RMVar_hsa_circ_78640,RMVar_hsa_circ_188412,RMVar_hsa_circ_188414,RMVar_hsa_circ_188413,RMVar_hsa_circ_188411,RMVar_hsa_circ_370615,RMVar_hsa_circ_188409,RMVar_hsa_circ_188416 69232 RMVar_ID_69232 Human_SNP_ID_636899432 m1A Human chr18 - 7021104 7021104 7021104 AAGAAGAGTGACCAGCGTGGGAAGACGGGCCCAGGCAAGTAGGCAGGCCCTGCCCGAGGTAGACA AAGAAGAGTGACCAGCGTGGGAAGACGGGCCCGGGCAAGTAGGCAGGCCCTGCCCGAGGTAGACA T C LAMA1 Ensembl:ENSG00000101680 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7020733..7021142 26863196 MeRIP-seq:(Medium) rs1179564485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79821,RMVar_hsa_circ_99906,RMVar_hsa_circ_97602,RMVar_hsa_circ_188399,RMVar_hsa_circ_188401,RMVar_hsa_circ_87091,RMVar_hsa_circ_188400,RMVar_hsa_circ_333865,RMVar_hsa_circ_28270,RMVar_hsa_circ_188402,RMVar_hsa_circ_119733,RMVar_hsa_circ_7723,RMVar_hsa_circ_188404,RMVar_hsa_circ_126989,RMVar_hsa_circ_118131,RMVar_hsa_circ_188407,RMVar_hsa_circ_188408,RMVar_hsa_circ_376070,RMVar_hsa_circ_369856,RMVar_hsa_circ_110749,RMVar_hsa_circ_116237,RMVar_hsa_circ_188410,RMVar_hsa_circ_28802,RMVar_hsa_circ_78640,RMVar_hsa_circ_188412,RMVar_hsa_circ_188414,RMVar_hsa_circ_188413,RMVar_hsa_circ_188411,RMVar_hsa_circ_370615,RMVar_hsa_circ_188409,RMVar_hsa_circ_188416 69233 RMVar_ID_69233 Human_SNP_ID_637043644 m1A Human chr18 - 7568593 7568593 7568593 CGCGGCGCTCCGCTAGGGGGACGAGGGTGGGGAGGGGGAGCCCAGCGGGGCGCAGGGCCGTGGCC CGCGGCGCTCCGCTAGGGGGACGAGGGTGGGGGGGGGGAGCCCAGCGGGGCGCAGGGCCGTGGCC T C lnc-LAMA1-8 RNACentral:URS0000D5C58A lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:7568588..7568723 32194978 MeRIP-seq:(Medium) rs1456593608 Functional Loss SNV dbSNP153 33..33 33 - - - 69234 RMVar_ID_69234 Human_SNP_ID_637044576 m1A Human chr18 + 7573090 7573090 7573090 GTAGTGCCCCCATCATTGGTGAGGAGGCTGGCAAGGCCAGGGCATAATTAAGGGTCTGGGAGTAT GTAGTGCCCCCATCATTGGTGAGGAGGCTGGCCAGGCCAGGGCATAATTAAGGGTCTGGGAGTAT A C PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:7573088..7573161 26863196 MeRIP-seq:(Medium) rs1294654415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2548788 69235 RMVar_ID_69235 Human_SNP_ID_637072464 m1A Human chr18 + 7693766 7693766 7693766 AGTAAATACACTTAAGGAAAATCTGGGAAGACATCATGGAGGAAGCTGGATTTGCACTGGGCTTG AGTAAATACACTTAAGGAAAATCTGGGAAGACCTCATGGAGGAAGCTGGATTTGCACTGGGCTTG A C PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7693763..7693903 26863196 MeRIP-seq:(Medium) rs1183902802 Functional Loss SNV dbSNP153 33..33 33 - - - 69236 RMVar_ID_69236 Human_SNP_ID_637072465 m1A Human chr18 + 7693766 7693766 7693766 AGTAAATACACTTAAGGAAAATCTGGGAAGACATCATGGAGGAAGCTGGATTTGCACTGGGCTTG AGTAAATACACTTAAGGAAAATCTGGGAAGACGTCATGGAGGAAGCTGGATTTGCACTGGGCTTG A G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7693763..7693903 26863196 MeRIP-seq:(Medium) rs1183902802 Functional Loss SNV dbSNP153 33..33 33 - - - 69237 RMVar_ID_69237 Human_SNP_ID_637130869 m1A Human chr18 + 7940522 7940522 7940522 GAGATGGAGTTGGCTCTGGGGGATGGGTGGGAAGCATTCTAGGAGGAGGAAGAGGTCTCAAGGAA GAGATGGAGTTGGCTCTGGGGGATGGGTGGGACGCATTCTAGGAGGAGGAAGAGGTCTCAAGGAA A C PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7940472..7940602 26863196 MeRIP-seq:(Medium) rs1174541966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356193,RMVar_hsa_circ_328906,RMVar_hsa_circ_57848,RMVar_hsa_circ_126233,RMVar_hsa_circ_17900,RMVar_hsa_circ_34853,RMVar_hsa_circ_23468,RMVar_hsa_circ_188440,RMVar_hsa_circ_188441,RMVar_hsa_circ_375266,RMVar_hsa_circ_5073,RMVar_hsa_circ_74371,RMVar_hsa_circ_188444,RMVar_hsa_circ_51825,RMVar_hsa_circ_297908,RMVar_hsa_circ_22449,RMVar_hsa_circ_348567,RMVar_hsa_circ_349780,RMVar_hsa_circ_15379,RMVar_hsa_circ_87724,RMVar_hsa_circ_188446,RMVar_hsa_circ_188447 69238 RMVar_ID_69238 Human_SNP_ID_637148188 m1A Human chr18 - 8010651 8010651 8010651 AAGGCTGTCTCTCCCTCCATCTCACCAAGTCCATGGGCTCTTCCATCCTCCTTAACCCACCTGCC AAGGCTGTCTCTCCCTCCATCTCACCAAGTCCGTGGGCTCTTCCATCCTCCTTAACCCACCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:8010639..8010732 26863196 MeRIP-seq:(Medium) rs1032128736 Functional Loss SNV dbSNP153 33..33 33 - - - 69239 RMVar_ID_69239 Human_SNP_ID_637203408 m1A Human chr18 + 8240721 8240718 8240722 GAGAAAGAGAGAAAGAAAGAAGGAAAGAAGAGAAAGAAAGAAATTGAAAGTTTGTGGCAACCCGC GAGAAAGAGAGAAAGAAAGAAGGAAAGAAG____AGAAAGAAATTGAAAGTTTGTGGCAACCCGC GAGAA G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8240712..8240784 26863196 MeRIP-seq:(Medium) rs1248271887 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_8867,RMVar_hsa_circ_57848,RMVar_hsa_circ_126233,RMVar_hsa_circ_188441,RMVar_hsa_circ_5073,RMVar_hsa_circ_101197,RMVar_hsa_circ_349780,RMVar_hsa_circ_15379,RMVar_hsa_circ_188449,RMVar_hsa_circ_111856,RMVar_hsa_circ_188453,RMVar_hsa_circ_188451,RMVar_hsa_circ_309097,RMVar_hsa_circ_115544,RMVar_hsa_circ_100096,RMVar_hsa_circ_188452,RMVar_hsa_circ_188460,RMVar_hsa_circ_88399,RMVar_hsa_circ_188461,RMVar_hsa_circ_24568,RMVar_hsa_circ_53051,RMVar_hsa_circ_188466,RMVar_hsa_circ_321242 69240 RMVar_ID_69240 Human_SNP_ID_637320022 m1A Human chr18 + 8705701 8705701 8705701 ACTGAACGGCCCCGCGGGCGGAGGTGCCCCGGACGCGAAGCTGCAGCCGCCCGGCCAGCACCACC ACTGAACGGCCCCGCGGGCGGAGGTGCCCCGGCCGCGAAGCTGCAGCCGCCCGGCCAGCACCACC A C MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr18:8705651..8705725;chr18:8705244..8707455 26863196 MeRIP-seq:(Medium) rs948113406 Functional Loss SNV dbSNP153 33..33 33 - - - 69241 RMVar_ID_69241 Human_SNP_ID_637320035 m1A Human chr18 + 8705749 8705749 8705749 GCCCGGCCAGCACCACCGCCACCACCACCTCCACCCGGTGGCCGAAAGGCGGCGGCTGCACCGTG GCCCGGCCAGCACCACCGCCACCACCACCTCCTCCCGGTGGCCGAAAGGCGGCGGCTGCACCGTG A T MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:8705316..8706425 26863196 MeRIP-seq:(Medium) rs1490649542 Functional Loss SNV dbSNP153 33..33 33 - - - 69242 RMVar_ID_69242 Human_SNP_ID_637320146 m1A Human chr18 + 8706177 8706177 8706177 CCAAGCGCGGCTCCCGGGCGCCACCCGCCCGCACCGTCGGCCCCCCGACCCCGGCCGCCCGGATC CCAAGCGCGGCTCCCGGGCGCCACCCGCCCGCGCCGTCGGCCCCCCGACCCCGGCCGCCCGGATC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:8706126..8706500 26863196 MeRIP-seq:(Medium) rs1336781174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9327698 69243 RMVar_ID_69243 Human_SNP_ID_637320181 m1A Human chr18 + 8706285 8706285 8706285 CCCGCTGCTCGCGCATCAGCCACACGGACAGCAGCTCCGACCTCTCTGACTGCCCCTCCGAACCC CCCGCTGCTCGCGCATCAGCCACACGGACAGCGGCTCCGACCTCTCTGACTGCCCCTCCGAACCC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:8706197..8706354 26863196 MeRIP-seq:(Medium) rs1320347690 Functional Loss SNV dbSNP153 33..33 33 - - - 69244 RMVar_ID_69244 Human_SNP_ID_637320333 m1A Human chr18 + 8706703 8706703 8706703 GCGGGAGATGGAGGAGCTGCGCTCGGAGAACGACTATCTCAAGGTGAGCCGCGCCTCGGCCGCAG GCGGGAGATGGAGGAGCTGCGCTCGGAGAACGGCTATCTCAAGGTGAGCCGCGCCTCGGCCGCAG A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:8706598..8706729 26863196 MeRIP-seq:(Medium) rs1438073631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905665,Human_RBP_ID_3953673,Human_RBP_ID_5369008,Human_RBP_ID_9291050,Human_RBP_ID_19087415 Human_Splice_Rec_1893033 69245 RMVar_ID_69245 Human_SNP_ID_637320334 m1A Human chr18 + 8706706 8706706 8706706 GGAGATGGAGGAGCTGCGCTCGGAGAACGACTATCTCAAGGTGAGCCGCGCCTCGGCCGCAGGTG GGAGATGGAGGAGCTGCGCTCGGAGAACGACTGTCTCAAGGTGAGCCGCGCCTCGGCCGCAGGTG A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr18:8705236..8706725;chr18:8705276..8706738 26863196 MeRIP-seq:(Medium) rs998622079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905665,Human_RBP_ID_3953673,Human_RBP_ID_5369008,Human_RBP_ID_9291050,Human_RBP_ID_19087415 Human_Splice_Rec_1893033 69246 RMVar_ID_69246 Human_SNP_ID_637323671 m1A Human chr18 - 8718632 8718632 8718632 CCACCCCCTCACTCACCTTCAAGTCCTGCTCCAGGCTTCGAATAAGCTCACCATCCACCTGACCC CCACCCCCTCACTCACCTTCAAGTCCTGCTCCGGGCTTCGAATAAGCTCACCATCCACCTGACCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:8718426..8718738 26863196 MeRIP-seq:(Medium) rs1194002289 Functional Loss SNV dbSNP153 33..33 33 - - - 69247 RMVar_ID_69247 Human_SNP_ID_637324103 m1A Human chr18 - 8720384 8720384 8720384 TTTCATCCTCAGCTTTAGCGCGCTTTTCCTCCACCGTCTTAAGTTCGTGGTGCAATCTGACAGAT TTTCATCCTCAGCTTTAGCGCGCTTTTCCTCCGCCGTCTTAAGTTCGTGGTGCAATCTGACAGAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:8720283..8720475 26863196 MeRIP-seq:(Medium) rs766484472 Functional Loss SNV dbSNP153 33..33 33 - - - 69248 RMVar_ID_69248 Human_SNP_ID_637341198 m1A Human chr18 - 8784766 8784766 8784766 GTCCCGGGACACGGAAGTCACAGTGGAGAGGAAGCTAGAGGACTCTGTGAGGTGGGGCAAGGGGG GTCCCGGGACACGGAAGTCACAGTGGAGAGGACGCTAGAGGACTCTGTGAGGTGGGGCAAGGGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8784716..8784840 26863196 MeRIP-seq:(Medium) rs1344947693 Functional Loss SNV dbSNP153 33..33 33 - - - 69249 RMVar_ID_69249 Human_SNP_ID_637341816 m1A Human chr18 + 8786021 8786007 8786022 GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGAGCTGCACCGCCGCGCAGACGGGGACACCGGGA GCGGGAGAGCCTGCGCCTC_______________CTGCACCGCCGCGCAGACGGGGACACCGGGA CCGAGCCGCGCGGGAG C MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:8785971..8786060 26863196 MeRIP-seq:(Medium) rs569097168 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_9291053 Human_Splice_Rec_1893042,Human_Splice_Rec_1893043,Human_Splice_Rec_1893068,Human_Splice_Rec_1893069,Human_Splice_Rec_1893098,Human_Splice_Rec_1893099,Human_Splice_Rec_1893136,Human_Splice_Rec_1893137,Human_Splice_Rec_1893162,Human_Splice_Rec_1893163,Human_Splice_Rec_1893174,Human_Splice_Rec_1893176,Human_Splice_Rec_1893177 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_82388,RMVar_hsa_circ_188484,RMVar_hsa_circ_75218,RMVar_hsa_circ_268080,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_265351,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_347398,RMVar_hsa_circ_37579,RMVar_hsa_circ_188489 69250 RMVar_ID_69250 Human_SNP_ID_637341833 m1A Human chr18 + 8786021 8786021 8786021 GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGAGCTGCACCGCCGCGCAGACGGGGACACCGGGA GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGGGCTGCACCGCCGCGCAGACGGGGACACCGGGA A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:8785971..8786060 26863196 MeRIP-seq:(Medium) rs753490941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9291053 Human_Splice_Rec_1893042,Human_Splice_Rec_1893043,Human_Splice_Rec_1893068,Human_Splice_Rec_1893069,Human_Splice_Rec_1893098,Human_Splice_Rec_1893099,Human_Splice_Rec_1893136,Human_Splice_Rec_1893137,Human_Splice_Rec_1893162,Human_Splice_Rec_1893163,Human_Splice_Rec_1893174,Human_Splice_Rec_1893176,Human_Splice_Rec_1893177 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_82388,RMVar_hsa_circ_188484,RMVar_hsa_circ_75218,RMVar_hsa_circ_268080,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_265351,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_347398,RMVar_hsa_circ_37579,RMVar_hsa_circ_188489 69251 RMVar_ID_69251 Human_SNP_ID_637341834 m1A Human chr18 + 8786021 8786021 8786021 GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGAGCTGCACCGCCGCGCAGACGGGGACACCGGGA GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGTGCTGCACCGCCGCGCAGACGGGGACACCGGGA A T MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:8785971..8786060 26863196 MeRIP-seq:(Medium) rs753490941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9291053 Human_Splice_Rec_1893042,Human_Splice_Rec_1893043,Human_Splice_Rec_1893068,Human_Splice_Rec_1893069,Human_Splice_Rec_1893098,Human_Splice_Rec_1893099,Human_Splice_Rec_1893136,Human_Splice_Rec_1893137,Human_Splice_Rec_1893162,Human_Splice_Rec_1893163,Human_Splice_Rec_1893174,Human_Splice_Rec_1893176,Human_Splice_Rec_1893177 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_82388,RMVar_hsa_circ_188484,RMVar_hsa_circ_75218,RMVar_hsa_circ_268080,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_265351,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_347398,RMVar_hsa_circ_37579,RMVar_hsa_circ_188489 69252 RMVar_ID_69252 Human_SNP_ID_637342072 m1A Human chr18 - 8786213 8786203 8786213 AAAATGGGTTTGCTGTCAAGTGAGTTCCACCTAGTTCCACCTCCTCCTGCCATGTTCCCTCAGGG AAAATGGGTTTGCTGTCAAGTGAGTTCCACCT__________CCTCCTGCCATGTTCCCTCAGGG GAGGTGGAACT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:8786211..8786361 32194978 MeRIP-seq:(Medium) rs751561680 Functional Loss DEL dbSNP153 33..42 33 - - - 69253 RMVar_ID_69253 Human_SNP_ID_637344734 m1A Human chr18 + 8796283 8796283 8796283 ATGCCTTGAGGTGGAAAGAACTGGAAATGCACAGCCTGGCTTTGCAAAACACCCTCCATGAGCGA ATGCCTTGAGGTGGAAAGAACTGGAAATGCACTGCCTGGCTTTGCAAAACACCCTCCATGAGCGA A T MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8796195..8796313 26863196 MeRIP-seq:(Medium) rs758726355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905467 Human_Splice_Rec_1893044,Human_Splice_Rec_1893070,Human_Splice_Rec_1893102,Human_Splice_Rec_1893140,Human_Splice_Rec_1893164,Human_Splice_Rec_1893180 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_75218,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_39604,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_37579,RMVar_hsa_circ_295583,RMVar_hsa_circ_188489,RMVar_hsa_circ_46534,RMVar_hsa_circ_17490 69254 RMVar_ID_69254 Human_SNP_ID_637348926 m1A Human chr18 + 8813034 8813034 8813034 GTTGGGAGAACTAGGCTCCTCCGCTGAGAGCAAGGGGGCCTTGAAGAAGGAGAGAGAGGTGCACC GTTGGGAGAACTAGGCTCCTCCGCTGAGAGCACGGGGGCCTTGAAGAAGGAGAGAGAGGTGCACC A C MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8812940..8813075 26863196 MeRIP-seq:(Medium) rs774769578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52056,Human_RBP_ID_3953498,Human_RBP_ID_26334299 Human_Splice_Rec_1893050,Human_Splice_Rec_1893076,Human_Splice_Rec_1893108,Human_Splice_Rec_1893146,Human_Splice_Rec_1893188,Human_Splice_Rec_1893200,Human_Splice_Rec_1893202,Human_Splice_Rec_1893204 RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_75218,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_352467,RMVar_hsa_circ_16758,RMVar_hsa_circ_295583,RMVar_hsa_circ_46534,RMVar_hsa_circ_99748,RMVar_hsa_circ_53050,RMVar_hsa_circ_188490 69255 RMVar_ID_69255 Human_SNP_ID_637348927 m1A Human chr18 + 8813034 8813034 8813034 GTTGGGAGAACTAGGCTCCTCCGCTGAGAGCAAGGGGGCCTTGAAGAAGGAGAGAGAGGTGCACC GTTGGGAGAACTAGGCTCCTCCGCTGAGAGCAGGGGGGCCTTGAAGAAGGAGAGAGAGGTGCACC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8812940..8813075 26863196 MeRIP-seq:(Medium) rs774769578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52056,Human_RBP_ID_3953498,Human_RBP_ID_26334299 Human_Splice_Rec_1893050,Human_Splice_Rec_1893076,Human_Splice_Rec_1893108,Human_Splice_Rec_1893146,Human_Splice_Rec_1893188,Human_Splice_Rec_1893200,Human_Splice_Rec_1893202,Human_Splice_Rec_1893204 RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_75218,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_352467,RMVar_hsa_circ_16758,RMVar_hsa_circ_295583,RMVar_hsa_circ_46534,RMVar_hsa_circ_99748,RMVar_hsa_circ_53050,RMVar_hsa_circ_188490 69256 RMVar_ID_69256 Human_SNP_ID_637351943 m1A Human chr18 + 8824941 8824941 8824941 CGACAGGACCGAGGTGGGGCGGGCAGGGCACGAGGACAGCACAGAGCCTTTCCCCGACTCCTCCT CGACAGGACCGAGGTGGGGCGGGCAGGGCACGGGGACAGCACAGAGCCTTTCCCCGACTCCTCCT A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8824837..8825010 26863196 MeRIP-seq:(Medium) rs1452769880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52069 Human_miRNA_ID_3070012 RMVar_hsa_circ_99748,RMVar_hsa_circ_188490,RMVar_hsa_circ_188491,RMVar_hsa_circ_336156 69257 RMVar_ID_69257 Human_SNP_ID_637352159 m1A Human chr18 - 8825304 8825304 8825304 TCTCCAGGCTGTGCAGTGGGGAGGCAAACCCCAGGGAGGTACAGAGGGGACTATCAAGGGGGCGC TCTCCAGGCTGTGCAGTGGGGAGGCAAACCCCGGGGAGGTACAGAGGGGACTATCAAGGGGGCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:8825255..8825356 32194978 MeRIP-seq:(Medium) rs1190226406 Functional Loss SNV dbSNP153 33..33 33 - - - 69258 RMVar_ID_69258 Human_SNP_ID_637352376 m1A Human chr18 + 8825822 8825822 8825822 CCACCACCACAAGGGAGAGCCCCGTGCACACCACCATTAATGATGGCCTCTCCAGCCTCTTCAAC CCACCACCACAAGGGAGAGCCCCGTGCACACCGCCATTAATGATGGCCTCTCCAGCCTCTTCAAC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:8825776..8825850 26863196 MeRIP-seq:(Medium) rs747047832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99748,RMVar_hsa_circ_188490,RMVar_hsa_circ_188491,RMVar_hsa_circ_336156 69259 RMVar_ID_69259 Human_SNP_ID_637352380 m1A Human chr18 - 8825826 8825826 8825826 TGATGTTGAAGAGGCTGGAGAGGCCATCATTAATGGTGGTGTGCACGGGGCTCTCCCTTGTGGTG TGATGTTGAAGAGGCTGGAGAGGCCATCATTAGTGGTGGTGTGCACGGGGCTCTCCCTTGTGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:8825776..8825875 26863196 MeRIP-seq:(Medium) rs1444105986 Functional Loss SNV dbSNP153 33..33 33 - - - 69260 RMVar_ID_69260 Human_SNP_ID_637423630 m1A Human chr18 - 9102751 9102751 9102751 GGCCAGCCGCCCGGGCCCGGAGCGCCGCGGAGAAGAACATGGCGGGCCACACTGTTCACCTTCCC GGCCAGCCGCCCGGGCCCGGAGCGCCGCGGAGGAGAACATGGCGGGCCACACTGTTCACCTTCCC T C NDUFV2-AS1 RNACentral:URS0000D57469 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:9102701..9117900;chr18:9102701..9102856;chr18:9102701..9102848 26863196 MeRIP-seq:(Medium) rs758463496 Functional Loss SNV dbSNP153 33..33 33 - - - 69261 RMVar_ID_69261 Human_SNP_ID_637423669 m1A Human chr18 - 9102784 9102784 9102784 TCAGCTTGAGCCTCCTTACCCAGTGGGCGGTGAGGCCAGCCGCCCGGGCCCGGAGCGCCGCGGAG TCAGCTTGAGCCTCCTTACCCAGTGGGCGGTGGGGCCAGCCGCCCGGGCCCGGAGCGCCGCGGAG T C NDUFV2-AS1 RNACentral:URS0000D57469 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:9102651..9102843 26863410 MeRIP-seq:(Medium) rs1233607338 Functional Loss SNV dbSNP153 33..33 33 - - - 69262 RMVar_ID_69262 Human_SNP_ID_637423681 m1A Human chr18 - 9102795 9102795 9102795 CAGCGCCGGGCTCAGCTTGAGCCTCCTTACCCAGTGGGCGGTGAGGCCAGCCGCCCGGGCCCGGA CAGCGCCGGGCTCAGCTTGAGCCTCCTTACCCGGTGGGCGGTGAGGCCAGCCGCCCGGGCCCGGA T C NDUFV2-AS1 RNACentral:URS0000D57469 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:9102763..9102890 26863196 MeRIP-seq:(Medium) rs751550238 Functional Loss SNV dbSNP153 33..33 33 - - - 69263 RMVar_ID_69263 Human_SNP_ID_637432690 m1A Human chr18 - 9137516 9137503 9137516 GCGTCGGCGCACGCTCGGCGGCTGGCGGCGGGAACGCGCGGCGGGCCGGGCGCGCCCCCGCCCCC GCGTCGGCGCACGCTCGGCGGCTGGCGGCGGG_____________CCGGGCGCGCCCCCGCCCCC GCCCGCCGCGCGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:9137493..9137621 26863196 MeRIP-seq:(Medium) rs1242042547 Functional Loss DEL dbSNP153 33..45 33 - - - 69264 RMVar_ID_69264 Human_SNP_ID_637485538 m1A Human chr18 + 9334872 9334872 9334872 AAAGCCGCCGCAGCGCGCCCCGGGCTCGGCCGACCCGGCGGGGATCTAGGGGTGGGCGACTTCGC AAAGCCGCCGCAGCGCGCCCCGGGCTCGGCCGCCCCGGCGGGGATCTAGGGGTGGGCGACTTCGC A C TWSG1 Ensembl:ENSG00000128791 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:9334831..9334959 26863196 MeRIP-seq:(Medium) rs1403062958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238557,Human_RBP_ID_4493934,Human_RBP_ID_5319524,Human_RBP_ID_9083761,Human_RBP_ID_18420786 Human_Splice_Rec_1893403,Human_Splice_Rec_1893415,Human_Splice_Rec_1893423 RMVar_hsa_circ_77931,RMVar_hsa_circ_188545 69265 RMVar_ID_69265 Human_SNP_ID_637485539 m1A Human chr18 + 9334872 9334872 9334872 AAAGCCGCCGCAGCGCGCCCCGGGCTCGGCCGACCCGGCGGGGATCTAGGGGTGGGCGACTTCGC AAAGCCGCCGCAGCGCGCCCCGGGCTCGGCCGTCCCGGCGGGGATCTAGGGGTGGGCGACTTCGC A T TWSG1 Ensembl:ENSG00000128791 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:9334831..9334959 26863196 MeRIP-seq:(Medium) rs1403062958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238557,Human_RBP_ID_4493934,Human_RBP_ID_5319524,Human_RBP_ID_9083761,Human_RBP_ID_18420786 Human_Splice_Rec_1893403,Human_Splice_Rec_1893415,Human_Splice_Rec_1893423 RMVar_hsa_circ_77931,RMVar_hsa_circ_188545 69266 RMVar_ID_69266 Human_SNP_ID_637485545 m1A Human chr18 + 9334883 9334883 9334883 AGCGCGCCCCGGGCTCGGCCGACCCGGCGGGGATCTAGGGGTGGGCGACTTCGCGGGACCGTGGC AGCGCGCCCCGGGCTCGGCCGACCCGGCGGGGTTCTAGGGGTGGGCGACTTCGCGGGACCGTGGC A T TWSG1 Ensembl:ENSG00000128791 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9334654..9334896 26863196 MeRIP-seq:(Medium) rs1409876740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238557,Human_RBP_ID_4493934,Human_RBP_ID_5319524,Human_RBP_ID_5468106,Human_RBP_ID_9083761,Human_RBP_ID_9327707,Human_RBP_ID_18420786 Human_Splice_Rec_1893403,Human_Splice_Rec_1893415,Human_Splice_Rec_1893423 RMVar_hsa_circ_77931,RMVar_hsa_circ_188545 69267 RMVar_ID_69267 Human_SNP_ID_637518462 m1A Human chr18 + 9475602 9475578 9475603 GGGGCGCCCGAGGCCGGCCTGGGGCGCAGCGCAGGAGGCGGCTCCGGTGGCTGCGGCGGCAGCGT GGGGCGCCC_________________________GAGGCGGCTCCGGTGGCTGCGGCGGCAGCGT CGAGGCCGGCCTGGGGCGCAGCGCAG C RALBP1 Ensembl:ENSG00000017797 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr18:9475551..9475700;chr18:9475551..9475705 26863196 MeRIP-seq:(Medium) rs1194253801 Functional Loss DEL dbSNP153 10..34 33 - - - Human_RBP_ID_768862,Human_RBP_ID_822944,Human_RBP_ID_905668,Human_RBP_ID_4493559,Human_RBP_ID_5319586,Human_RBP_ID_8232795,Human_RBP_ID_9290941,Human_RBP_ID_18420647,Human_RBP_ID_22064177,Human_RBP_ID_24545304,Human_RBP_ID_26334309,Human_RBP_ID_26769686,Human_RBP_ID_27814495 Human_Splice_Rec_1893447,Human_Splice_Rec_1893453,Human_Splice_Rec_1893471 Human_miRNA_ID_3010942 RMVar_hsa_circ_124665,RMVar_hsa_circ_188551 69268 RMVar_ID_69268 Human_SNP_ID_637518471 m1A Human chr18 + 9475602 9475602 9475602 GGGGCGCCCGAGGCCGGCCTGGGGCGCAGCGCAGGAGGCGGCTCCGGTGGCTGCGGCGGCAGCGT GGGGCGCCCGAGGCCGGCCTGGGGCGCAGCGCGGGAGGCGGCTCCGGTGGCTGCGGCGGCAGCGT A G RALBP1 Ensembl:ENSG00000017797 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr18:9475551..9475700;chr18:9475551..9475705 26863196 MeRIP-seq:(Medium) rs1316425397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768862,Human_RBP_ID_822944,Human_RBP_ID_905668,Human_RBP_ID_4493559,Human_RBP_ID_5319586,Human_RBP_ID_8232795,Human_RBP_ID_9290941,Human_RBP_ID_18420647,Human_RBP_ID_22064177,Human_RBP_ID_24545304,Human_RBP_ID_26334309,Human_RBP_ID_26769686,Human_RBP_ID_27814495 Human_Splice_Rec_1893447,Human_Splice_Rec_1893453,Human_Splice_Rec_1893471 Human_miRNA_ID_3010942 RMVar_hsa_circ_124665,RMVar_hsa_circ_188551 69269 RMVar_ID_69269 Human_SNP_ID_637519070 m1A Human chr18 - 9477812 9477812 9477812 TACCTAAATGCCCATTCTTTCTATGCCTGTACACTCCTGATTTTCATCACCTTCTACATAGTTTT TACCTAAATGCCCATTCTTTCTATGCCTGTACGCTCCTGATTTTCATCACCTTCTACATAGTTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:9477809..9477904 26863196 MeRIP-seq:(Medium) rs575495611 Functional Loss SNV dbSNP153 33..33 33 - - - 69270 RMVar_ID_69270 Human_SNP_ID_637527558 m1A Human chr18 - 9512938 9512938 9512938 TTAGCAGAGTCACCTAACACCAAGGAACAAAAACACCACAGCATTTACAAATCAAAAATATTTTC TTAGCAGAGTCACCTAACACCAAGGAACAAAACCACCACAGCATTTACAAATCAAAAATATTTTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:9512935..9513225 26863196 MeRIP-seq:(Medium) rs532956623 Functional Loss SNV dbSNP153 33..33 33 - - - 69271 RMVar_ID_69271 Human_SNP_ID_637527569 m1A Human chr18 + 9513002 9513002 9513002 ATGTTTTTTCTCTTGGTGCAGGTGTAATGGATAGGTAACAGAGAAGACCTCGTCCCTTCCTAGTC ATGTTTTTTCTCTTGGTGCAGGTGTAATGGATGGGTAACAGAGAAGACCTCGTCCCTTCCTAGTC A G RALBP1 Ensembl:ENSG00000017797 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:9512994..9513145 32194978 MeRIP-seq:(Medium) rs1376343036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906815,Human_RBP_ID_1552480,Human_RBP_ID_4493567,Human_RBP_ID_22661178,Human_RBP_ID_26334311,Human_RBP_ID_26814534 Human_Splice_Rec_1893430,Human_Splice_Rec_1893450,Human_Splice_Rec_1893454,Human_Splice_Rec_1893472,Human_Splice_Rec_1893476,Human_Splice_Rec_1893482 Human_miRNA_ID_3118851 RMVar_hsa_circ_9846,RMVar_hsa_circ_124665,RMVar_hsa_circ_275129,RMVar_hsa_circ_330684,RMVar_hsa_circ_188551,RMVar_hsa_circ_358618,RMVar_hsa_circ_284331,RMVar_hsa_circ_22160,RMVar_hsa_circ_188552,RMVar_hsa_circ_188553 69272 RMVar_ID_69272 Human_SNP_ID_637529669 m1A Human chr18 + 9522306 9522306 9522306 ACCTTCCAGAGAATTTGCTTACCAAAGAGCTTATGCCCAGATTTGAAGAGGCTTGTGGGAGGACC ACCTTCCAGAGAATTTGCTTACCAAAGAGCTTGTGCCCAGATTTGAAGAGGCTTGTGGGAGGACC A G RALBP1 Ensembl:ENSG00000017797 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:9522255..9522356 32194978 MeRIP-seq:(Medium) rs142799309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511528,Human_RBP_ID_1012629,Human_RBP_ID_4497018,Human_RBP_ID_8828620,Human_RBP_ID_9290945,Human_RBP_ID_9379496,Human_RBP_ID_26334316 RMVar_hsa_circ_9846,RMVar_hsa_circ_124665,RMVar_hsa_circ_330684,RMVar_hsa_circ_188551,RMVar_hsa_circ_358618,RMVar_hsa_circ_22160,RMVar_hsa_circ_188554,RMVar_hsa_circ_111293,RMVar_hsa_circ_188555,RMVar_hsa_circ_309882,RMVar_hsa_circ_349515,RMVar_hsa_circ_275515 69273 RMVar_ID_69273 Human_SNP_ID_637533169 m1A Human chr18 - 9536167 9536167 9536167 AACAAAGAAAATTAATCTTCAAATAAGCTGACACTATCTGGAAAACTCATCTGTCCCTAAAGCCC AACAAAGAAAATTAATCTTCAAATAAGCTGACGCTATCTGGAAAACTCATCTGTCCCTAAAGCCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:9536117..9536225 32194978 MeRIP-seq:(Medium) rs900544591 Functional Loss SNV dbSNP153 33..33 33 - - - 69274 RMVar_ID_69274 Human_SNP_ID_637537258 m1A Human chr18 + 9550094 9550094 9550094 AAGACAAAGGCTTGCCGACCAGACCACTTGGGACATCTGCCAAAGTTCTCCACAAGCTCATTGAT AAGACAAAGGCTTGCCGACCAGACCACTTGGGGCATCTGCCAAAGTTCTCCACAAGCTCATTGAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:9550075..9550176 32194978 MeRIP-seq:(Medium) rs374803778 Functional Loss SNV dbSNP153 33..33 33 - - - 69275 RMVar_ID_69275 Human_SNP_ID_637586113 m1A Human chr18 + 9742157 9742157 9742157 GGAAGGCAAGGTCAGACTGGATTGAGAGTTGCAACTGTGATTGAAGGCGGTCTTTCAAAGCAGGC GGAAGGCAAGGTCAGACTGGATTGAGAGTTGCGACTGTGATTGAAGGCGGTCTTTCAAAGCAGGC A G RAB31 Ensembl:ENSG00000168461 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:9742152..9742221 26863196 MeRIP-seq:(Medium) rs1300881157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110845,RMVar_hsa_circ_125830,RMVar_hsa_circ_188609,RMVar_hsa_circ_188611,RMVar_hsa_circ_97752,RMVar_hsa_circ_188610,RMVar_hsa_circ_114651,RMVar_hsa_circ_188612 69276 RMVar_ID_69276 Human_SNP_ID_637596664 m1A Human chr18 + 9786069 9786068 9786070 TCAGACTCTGAGAAAGAAAGAGAGAAAGAGAAAGAGAGTAACAGAGAAGAGAAAGAAAAGAGAAT TCAGACTCTGAGAAAGAAAGAGAGAAAGAGAA__AGAGTAACAGAGAAGAGAAAGAAAAGAGAAT AAG A RAB31,ZNF415P1 Ensembl:ENSG00000168461,Ensembl:ENSG00000266127 Protein coding,Pseudogene intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9786066..9786149 26863196 MeRIP-seq:(Medium) rs889012093 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110845,RMVar_hsa_circ_125830,RMVar_hsa_circ_188609,RMVar_hsa_circ_188611,RMVar_hsa_circ_97752,RMVar_hsa_circ_188610,RMVar_hsa_circ_114651,RMVar_hsa_circ_188614,RMVar_hsa_circ_294303,RMVar_hsa_circ_188612,RMVar_hsa_circ_367434,RMVar_hsa_circ_291973,RMVar_hsa_circ_188616,RMVar_hsa_circ_98519,RMVar_hsa_circ_188615,RMVar_hsa_circ_188613 69277 RMVar_ID_69277 Human_SNP_ID_637605888 m1A Human chr18 - 9824383 9824361 9824383 ACACTCATATACACATACATCTACACACACACATACACATCTACACACACACACCTATACACACA ACACTCATATACACATACATCTACACACACAC______________________CTATACACACA GGTGTGTGTGTGTAGATGTGTAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9824377..9824464 26863196 MeRIP-seq:(Medium) rs1568188794 Functional Loss DEL dbSNP153 33..54 33 - - - 69278 RMVar_ID_69278 Human_SNP_ID_637605902 m1A Human chr18 - 9824383 9824382 9824384 ACACTCATATACACATACATCTACACACACACATACACATCTACACACACACACCTATACACACA ACACTCATATACACATACATCTACACACACA__TACACATCTACACACACACACCTATACACACA ATG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9824377..9824464 26863196 MeRIP-seq:(Medium) rs1317694384 Functional Loss DEL dbSNP153 32..33 33 - - - 69279 RMVar_ID_69279 Human_SNP_ID_637606786 m1A Human chr18 + 9828205 9828205 9828205 CCCTGCGCCTGCCCTGGGGAATAGTGGGAAAGATGGCGGGATGGTGTGGGTCTCAGAAGCATGCA CCCTGCGCCTGCCCTGGGGAATAGTGGGAAAGGTGGCGGGATGGTGTGGGTCTCAGAAGCATGCA A G RAB31 Ensembl:ENSG00000168461 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:9828197..9828264 26863196 MeRIP-seq:(Medium) rs1225630959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125830,RMVar_hsa_circ_188611,RMVar_hsa_circ_188614,RMVar_hsa_circ_367434,RMVar_hsa_circ_98519,RMVar_hsa_circ_188613,RMVar_hsa_circ_79742,RMVar_hsa_circ_188620,RMVar_hsa_circ_125806,RMVar_hsa_circ_328406,RMVar_hsa_circ_188624,RMVar_hsa_circ_188625,RMVar_hsa_circ_107573,RMVar_hsa_circ_188626 69280 RMVar_ID_69280 Human_SNP_ID_637609490 m1A Human chr18 - 9839415 9839415 9839415 CCCATGGTGGGGACTCTTCAAACTGCGAATCTACCAAGTATTCCTGTGAATAGGATTCTCCAACA CCCATGGTGGGGACTCTTCAAACTGCGAATCTTCCAAGTATTCCTGTGAATAGGATTCTCCAACA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:9839413..9839664 26863196 MeRIP-seq:(Medium) rs1184781422 Functional Loss SNV dbSNP153 33..33 33 - - - 69281 RMVar_ID_69281 Human_SNP_ID_637628403 m1A Human chr18 + 9914214 9914214 9914214 TCGCCGCCGTCGTCCCCCGCCCCCAGTCAGCAAACCGCCGCCGCGGGCGCGCCCCCGCTCTGCGC TCGCCGCCGTCGTCCCCCGCCCCCAGTCAGCATACCGCCGCCGCGGGCGCGCCCCCGCTCTGCGC A T VAPA Ensembl:ENSG00000101558 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9914001..9914350 26863196 MeRIP-seq:(Medium) rs1160291492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238531,Human_RBP_ID_511672,Human_RBP_ID_4493938,Human_RBP_ID_5319588,Human_RBP_ID_17381594,Human_RBP_ID_22533025,Human_RBP_ID_26814290 Human_miRNA_ID_2949733 RMVar_hsa_circ_110917,RMVar_hsa_circ_188630 69282 RMVar_ID_69282 Human_SNP_ID_637628433 m1A Human chr18 - 9914242 9914242 9914242 CCCTGAGGCGGACGCCATCGGAGAGACAGCGCAGAGCGGGGGCGCGCCCGCGGCGGCGGTTTGCT CCCTGAGGCGGACGCCATCGGAGAGACAGCGCGGAGCGGGGGCGCGCCCGCGGCGGCGGTTTGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:9914051..9914628 26863410 MeRIP-seq:(Medium) rs1423038905 Functional Loss SNV dbSNP153 33..33 33 - - - 69283 RMVar_ID_69283 Human_SNP_ID_637628434 m1A Human chr18 - 9914242 9914242 9914242 CCCTGAGGCGGACGCCATCGGAGAGACAGCGCAGAGCGGGGGCGCGCCCGCGGCGGCGGTTTGCT CCCTGAGGCGGACGCCATCGGAGAGACAGCGCCGAGCGGGGGCGCGCCCGCGGCGGCGGTTTGCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:9914051..9914628 26863410 MeRIP-seq:(Medium) rs1423038905 Functional Loss SNV dbSNP153 33..33 33 - - - 69284 RMVar_ID_69284 Human_SNP_ID_637630318 m1A Human chr18 + 9920007 9920004 9920008 TGAGACTTGGTGGTCTCTATGTGCACTGAGAGAAAAGGGTATGAATGTCTGAGATTTCTGCTTAT TGAGACTTGGTGGTCTCTATGTGCACTGAG____AAGGGTATGAATGTCTGAGATTTCTGCTTAT GAGAA G VAPA Ensembl:ENSG00000101558 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:9919992..9920162 26863196 MeRIP-seq:(Medium) rs1450725482 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_7116,Human_RBP_ID_13346810,Human_RBP_ID_17130172,Human_RBP_ID_23779886,Human_RBP_ID_24373696,Human_RBP_ID_27838984 69285 RMVar_ID_69285 Human_SNP_ID_637768467 m1A Human chr18 - 10454844 10454844 10454844 GGCCGGGGCTTCAGGCGGCTGCCGCGCGCCCCATGCCCGGCGGGCTAGGCGCGGGGCTGCGGGGC GGCCGGGGCTTCAGGCGGCTGCCGCGCGCCCCGTGCCCGGCGGGCTAGGCGCGGGGCTGCGGGGC T C lnc-PIEZO2-16 RNACentral:URS0000D57D77 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:10454813..10454940 26863196 MeRIP-seq:(Medium) rs941081145 Functional Loss SNV dbSNP153 33..33 33 - - - 69286 RMVar_ID_69286 Human_SNP_ID_637768471 m1A Human chr18 + 10454889 10454869 10454889 AGCCGCCTGAAGCCCCGGCCTGGCCCGGCCGCACCCGGCCGGAGGCGGAGGGCAGAGCGCGCGCC AGCCGCCTGAAGC____________________CCCGGCCGGAGGCGGAGGGCAGAGCGCGCGCC CCCCGGCCTGGCCCGGCCGCA C APCDD1 Ensembl:ENSG00000154856 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:10454847..10454931 26863196 MeRIP-seq:(Medium) rs1201699796 Functional Loss DEL dbSNP153 14..33 33 - - - 69287 RMVar_ID_69287 Human_SNP_ID_637768477 m1A Human chr18 + 10454889 10454879 10454889 AGCCGCCTGAAGCCCCGGCCTGGCCCGGCCGCACCCGGCCGGAGGCGGAGGGCAGAGCGCGCGCC AGCCGCCTGAAGCCCCGGCCTGG__________CCCGGCCGGAGGCGGAGGGCAGAGCGCGCGCC GCCCGGCCGCA G APCDD1 Ensembl:ENSG00000154856 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:10454847..10454931 26863196 MeRIP-seq:(Medium) rs1039117467 Functional Loss DEL dbSNP153 24..33 33 - - - 69288 RMVar_ID_69288 Human_SNP_ID_637787018 m1A Human chr18 + 10526134 10526134 10526134 GATGGCGGCTCAGAAGATAAACGAGGGGCTGGAACACCTCGCCAAAGCAGAGAAATAGTGAGTGA GATGGCGGCTCAGAAGATAAACGAGGGGCTGGCACACCTCGCCAAAGCAGAGAAATAGTGAGTGA A C NAPG Ensembl:ENSG00000134265 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:10526083..10526200 26863196 MeRIP-seq:(Medium) rs1157400204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905672,Human_RBP_ID_4494138,Human_RBP_ID_18420649,Human_RBP_ID_26334574,Human_RBP_ID_27814508 Human_Splice_Rec_1894005,Human_Splice_Rec_1894019,Human_Splice_Rec_1894041,Human_Splice_Rec_1894061,Human_Splice_Rec_1894075 69289 RMVar_ID_69289 Human_SNP_ID_637787831 m1A Human chr18 + 10528392 10528392 10528392 ACAGGTGGGCAGACAAGTTAACAGAGGACTAAAAATAGGATGTTCAGTGCTAGAATAGAAGTATT ACAGGTGGGCAGACAAGTTAACAGAGGACTAACAATAGGATGTTCAGTGCTAGAATAGAAGTATT A C NAPG Ensembl:ENSG00000134265 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:10528388..10528668 26863196 MeRIP-seq:(Medium) rs892467296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5189636,Human_RBP_ID_13244814 69290 RMVar_ID_69290 Human_SNP_ID_637787832 m1A Human chr18 + 10528392 10528392 10528392 ACAGGTGGGCAGACAAGTTAACAGAGGACTAAAAATAGGATGTTCAGTGCTAGAATAGAAGTATT ACAGGTGGGCAGACAAGTTAACAGAGGACTAAGAATAGGATGTTCAGTGCTAGAATAGAAGTATT A G NAPG Ensembl:ENSG00000134265 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:10528388..10528668 26863196 MeRIP-seq:(Medium) rs892467296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5189636,Human_RBP_ID_13244814 69291 RMVar_ID_69291 Human_SNP_ID_638089535 m1A Human chr18 + 11689307 11689307 11689307 CCGCTCTGGGCGTTAGCAAGTGATCTCCAGCCAAGGCGGCCGCCACCCCTTGCACACAGCAGAAA CCGCTCTGGGCGTTAGCAAGTGATCTCCAGCCCAGGCGGCCGCCACCCCTTGCACACAGCAGAAA A C GNAL Ensembl:ENSG00000141404 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:11689267..11689419 26863196 MeRIP-seq:(Medium) rs1417975139 Functional Loss SNV dbSNP153 33..33 33 - - - 69292 RMVar_ID_69292 Human_SNP_ID_638092033 m1A Human chr18 - 11697973 11697973 11697973 GGCATGTCCTCTCCGGGTGGCATGTGGTCCCCAGGTGGCATGTCCAACCTGGCCAGTGCACTAAT GGCATGTCCTCTCCGGGTGGCATGTGGTCCCCGGGTGGCATGTCCAACCTGGCCAGTGCACTAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:11697971..11698212 26863196 MeRIP-seq:(Medium) rs957961557 Functional Loss SNV dbSNP153 33..33 33 - - - 69293 RMVar_ID_69293 Human_SNP_ID_638129669 m1A Human chr18 - 11851476 11851476 11851476 CGGACGGCTCCTTTGGGTCGGCGGCCCGGCTGAGAAGCGCGCCGAAGGCAGAGAAGGTAAGGTAA CGGACGGCTCCTTTGGGTCGGCGGCCCGGCTGGGAAGCGCGCCGAAGGCAGAGAAGGTAAGGTAA T C CHMP1B-AS1 Ensembl:ENSG00000267165 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:11851426..11851711;chr18:11851426..11851756 26863196 MeRIP-seq:(Medium) rs1198095000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5584074 69294 RMVar_ID_69294 Human_SNP_ID_638129713 m1A Human chr18 + 11851558 11851558 11851558 GAAACACCTGTTCAACCTGAAGTTCGCGGCCAAAGAACTGAGTAGGAGTGCCAAAAAATGCGATA GAAACACCTGTTCAACCTGAAGTTCGCGGCCAGAGAACTGAGTAGGAGTGCCAAAAAATGCGATA A G GNAL,CHMP1B Ensembl:ENSG00000141404,Ensembl:ENSG00000255112 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:11851451..11851575 26863196 MeRIP-seq:(Medium) rs777911714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1547683,Human_RBP_ID_4482180,Human_RBP_ID_6667429,Human_RBP_ID_13247794,Human_RBP_ID_27460601 Human_miRNA_ID_416348 69295 RMVar_ID_69295 Human_SNP_ID_638129714 m1A Human chr18 + 11851558 11851558 11851558 GAAACACCTGTTCAACCTGAAGTTCGCGGCCAAAGAACTGAGTAGGAGTGCCAAAAAATGCGATA GAAACACCTGTTCAACCTGAAGTTCGCGGCCATAGAACTGAGTAGGAGTGCCAAAAAATGCGATA A T GNAL,CHMP1B Ensembl:ENSG00000141404,Ensembl:ENSG00000255112 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:11851451..11851575 26863196 MeRIP-seq:(Medium) rs777911714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1547683,Human_RBP_ID_4482180,Human_RBP_ID_6667429,Human_RBP_ID_13247794,Human_RBP_ID_27460601 Human_miRNA_ID_416348 69296 RMVar_ID_69296 Human_SNP_ID_638129884 m1A Human chr18 + 11852005 11852005 11852005 GGAAATGGCAGATGAGGCGGGCCTCGACCTCAACATGGAGCTGCCGCAGGGCCAGACCGGCTCCG GGAAATGGCAGATGAGGCGGGCCTCGACCTCAGCATGGAGCTGCCGCAGGGCCAGACCGGCTCCG A G GNAL,CHMP1B Ensembl:ENSG00000141404,Ensembl:ENSG00000255112 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:11851926..11852151 32194978 MeRIP-seq:(Medium) rs774638280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9379788,Human_RBP_ID_22446016 69297 RMVar_ID_69297 Human_SNP_ID_638129885 m1A Human chr18 + 11852005 11852005 11852005 GGAAATGGCAGATGAGGCGGGCCTCGACCTCAACATGGAGCTGCCGCAGGGCCAGACCGGCTCCG GGAAATGGCAGATGAGGCGGGCCTCGACCTCATCATGGAGCTGCCGCAGGGCCAGACCGGCTCCG A T GNAL,CHMP1B Ensembl:ENSG00000141404,Ensembl:ENSG00000255112 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:11851926..11852151 32194978 MeRIP-seq:(Medium) rs774638280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9379788,Human_RBP_ID_22446016 69298 RMVar_ID_69298 Human_SNP_ID_638132061 m1A Human chr18 + 11859937 11859937 11859937 ACCTGGCTAATTTTTGTAGTTTTCGTAGAGACAGGGTTTCACAATGTTGGCTAGGTTGGTCTCAA ACCTGGCTAATTTTTGTAGTTTTCGTAGAGACGGGGTTTCACAATGTTGGCTAGGTTGGTCTCAA A G GNAL Ensembl:ENSG00000141404 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:11859893..11860000 26863196 MeRIP-seq:(Medium) rs1231047050 Functional Loss SNV dbSNP153 33..33 33 - - - 69299 RMVar_ID_69299 Human_SNP_ID_638145569 m1A Human chr18 - 11908295 11908295 11908295 GGCTCCGGCTGCAGTTCCCGGGTCCCTCGGCCACCGAAGCCACCCTGCCCTGGTGAAAGGGCTCC GGCTCCGGCTGCAGTTCCCGGGTCCCTCGGCCTCCGAAGCCACCCTGCCCTGGTGAAAGGGCTCC T A MPPE1 Ensembl:ENSG00000154889 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:11908245..11908314 26863196 MeRIP-seq:(Medium) rs1418982907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4482294 Human_Splice_Rec_1895115,Human_Splice_Rec_1895135,Human_Splice_Rec_1895151,Human_Splice_Rec_1895173,Human_Splice_Rec_1895197,Human_Splice_Rec_1895211,Human_Splice_Rec_1895273,Human_Splice_Rec_1895289,Human_Splice_Rec_1895317,Human_Splice_Rec_1895329,Human_Splice_Rec_1895341,Human_Splice_Rec_1895357,Human_Splice_Rec_1895367,Human_Splice_Rec_1895373,Human_Splice_Rec_1895383,Human_Splice_Rec_1895389,Human_Splice_Rec_1895393,Human_Splice_Rec_1895401,Human_Splice_Rec_1895409,Human_Splice_Rec_1895419 69300 RMVar_ID_69300 Human_SNP_ID_638166461 m1A Human chr18 - 11981559 11981559 11981559 CCAGGCTCCACACTCCCTGTGCCTGCTCCCGCAGCTCTGTGCCTAGTCCGCCGCCCGTCCCACAC CCAGGCTCCACACTCCCTGTGCCTGCTCCCGCGGCTCTGTGCCTAGTCCGCCGCCCGTCCCACAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:11981501..11981775 26863196 MeRIP-seq:(Medium) rs1231546284 Functional Loss SNV dbSNP153 33..33 33 - - - 69301 RMVar_ID_69301 Human_SNP_ID_638171119 m1A Human chr18 + 11999010 11999010 11999010 CGAAGGAGTGGATAATTCCTTTGCCTGGGAGGAGGATGTTTGCATGTTTAACCCAAATCCCGTAC CGAAGGAGTGGATAATTCCTTTGCCTGGGAGGCGGATGTTTGCATGTTTAACCCAAATCCCGTAC A C IMPA2 Ensembl:ENSG00000141401 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:11999003..11999238 26863196 MeRIP-seq:(Medium) rs1270413219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22589306 69302 RMVar_ID_69302 Human_SNP_ID_638171132 m1A Human chr18 + 11999063 11999063 11999063 CAAATCCCGTACTTTTATTTCAGATCATCAGAAAAGCCCTTACTGAGGAAAAACGTGTCTCAACA CAAATCCCGTACTTTTATTTCAGATCATCAGAGAAGCCCTTACTGAGGAAAAACGTGTCTCAACA A G IMPA2 Ensembl:ENSG00000141401 Protein coding exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:11999051..11999075;chr18:11999051..11999100 26863196 MeRIP-seq:(Medium) rs745311348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52272,Human_RBP_ID_9379513 Human_Splice_Rec_1895424,Human_Splice_Rec_1895434,Human_Splice_Rec_1895448,Human_Splice_Rec_1895452,Human_Splice_Rec_1895466,Human_Splice_Rec_1895480,Human_Splice_Rec_1895492 RMVar_hsa_circ_188684,RMVar_hsa_circ_293099 69303 RMVar_ID_69303 Human_SNP_ID_638179015 m1A Human chr18 + 12028950 12028950 12028950 GGCCTGCACTGCTGGGATCTGGCGGCTGCCACAGTCATCATCAGAGAAGCAGGCGGCATCGTGAT GGCCTGCACTGCTGGGATCTGGCGGCTGCCACGGTCATCATCAGAGAAGCAGGCGGCATCGTGAT A G IMPA2 Ensembl:ENSG00000141401 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:12028899..12029029 26863196 MeRIP-seq:(Medium) rs761049420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504694 Human_Splice_Rec_1895445,Human_Splice_Rec_1895463,Human_Splice_Rec_1895477,Human_Splice_Rec_1895501,Human_Splice_Rec_1895513,Human_Splice_Rec_1895533 RMVar_hsa_circ_29819 69304 RMVar_ID_69304 Human_SNP_ID_638248816 m1A Human chr18 + 12307978 12307976 12307979 AGGGCCCGACTCGCGTCTCCCTCTGGCGGGGCACCACAAGGGGCAGCGAAACGGTGGTGGGGGCG AGGGCCCGACTCGCGTCTCCCTCTGGCGGGG___CACAAGGGGCAGCGAAACGGTGGTGGGGGCG GCAC G TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12307927..12308095 26863196 MeRIP-seq:(Medium) rs990714307 Functional Loss DEL dbSNP153 32..34 33 - - - 69305 RMVar_ID_69305 Human_SNP_ID_638249010 m1A Human chr18 - 12308303 12308298 12308304 GGTTCCCGCACTGGCCCGCCTGGATGTGCACGATCTCCCTCATGGCGGGCGCGGCTCTGCGCTAG GGTTCCCGCACTGGCCCGCCTGGATGTGCAC______CCTCATGGCGGGCGCGGCTCTGCGCTAG GGAGATC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr18:12308201..12308391;chr18:12308212..12308436 26863196 MeRIP-seq:(Medium) rs1406436322 Functional Loss DEL dbSNP153 32..37 33 - - - 69306 RMVar_ID_69306 Human_SNP_ID_638249159 m1A Human chr18 - 12308618 12308618 12308618 ACCCAGAGCCCGGGACGCCGCCACCCGCGCCCACCCCAGGCGCCCCGGCGGCCGAATTCCAGGCG ACCCAGAGCCCGGGACGCCGCCACCCGCGCCCCCCCCAGGCGCCCCGGCGGCCGAATTCCAGGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:12308610..12308750 26863196 MeRIP-seq:(Medium) rs937326026 Functional Loss SNV dbSNP153 33..33 33 - - - 69307 RMVar_ID_69307 Human_SNP_ID_638253244 m1A Human chr18 - 12325038 12325038 12325038 TGGCCTGCAACAAAGAGAGTCCCGTGCCGTTTAAACAGGAAAGGGCTGCGCCATCACCATGCTTG TGGCCTGCAACAAAGAGAGTCCCGTGCCGTTTGAACAGGAAAGGGCTGCGCCATCACCATGCTTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:12325026..12325150 26863196 MeRIP-seq:(Medium) rs1156517355 Functional Loss SNV dbSNP153 33..33 33 - - - 69308 RMVar_ID_69308 Human_SNP_ID_638254361 m1A Human chr18 + 12329219 12329219 12329219 GTGGGCGACAAAGAGAAAGCATCCCTTCCCACACGCCAAGAGTCCAGTGCAACGATCCCTGCCAC GTGGGCGACAAAGAGAAAGCATCCCTTCCCACGCGCCAAGAGTCCAGTGCAACGATCCCTGCCAC A G TUBB6 Ensembl:ENSG00000176014 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:12329169..12329691 32194978 MeRIP-seq:(Medium) rs1351363401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1895650 69309 RMVar_ID_69309 Human_SNP_ID_638254368 m1A Human chr18 + 12329232 12329232 12329232 AGAAAGCATCCCTTCCCACACGCCAAGAGTCCAGTGCAACGATCCCTGCCACACGGTCAGCCGAC AGAAAGCATCCCTTCCCACACGCCAAGAGTCCGGTGCAACGATCCCTGCCACACGGTCAGCCGAC A G TUBB6 Ensembl:ENSG00000176014 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12329181..12329388 26863196 MeRIP-seq:(Medium) rs371759084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1895650 69310 RMVar_ID_69310 Human_SNP_ID_638258616 m1A Human chr18 - 12344183 12344183 12344183 GAGGAGAAGAAGACTGTGGCATACCACGAAGCAGGCCATGCGGTTGCCGGCTGGTATCTGGAGCA GAGGAGAAGAAGACTGTGGCATACCACGAAGCGGGCCATGCGGTTGCCGGCTGGTATCTGGAGCA T C AFG3L2 Ensembl:ENSG00000141385 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:12344082..12344183 32194978 MeRIP-seq:(Medium) rs1186991915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906834,Human_RBP_ID_4482499,Human_RBP_ID_8828776,Human_RBP_ID_24545310,Human_RBP_ID_26334331,Human_RBP_ID_27814512 Human_Splice_Rec_1895736,Human_Splice_Rec_1895737,Human_Splice_Rec_1895744 RMVar_hsa_circ_12567,RMVar_hsa_circ_78091,RMVar_hsa_circ_123567,RMVar_hsa_circ_107465,RMVar_hsa_circ_188692,RMVar_hsa_circ_188693,RMVar_hsa_circ_188694,RMVar_hsa_circ_377215,RMVar_hsa_circ_379014,RMVar_hsa_circ_344321,RMVar_hsa_circ_29644,RMVar_hsa_circ_43656,RMVar_hsa_circ_16633,RMVar_hsa_circ_22927,RMVar_hsa_circ_33127,RMVar_hsa_circ_116357,RMVar_hsa_circ_337274,RMVar_hsa_circ_343859,RMVar_hsa_circ_355866,RMVar_hsa_circ_342237,RMVar_hsa_circ_87134,RMVar_hsa_circ_92799,RMVar_hsa_circ_48703,RMVar_hsa_circ_188695,RMVar_hsa_circ_188697,RMVar_hsa_circ_11484,RMVar_hsa_circ_188698,RMVar_hsa_circ_188696,RMVar_hsa_circ_328229,RMVar_hsa_circ_343094,RMVar_hsa_circ_121369,RMVar_hsa_circ_188699 69311 RMVar_ID_69311 Human_SNP_ID_638262730 m1A Human chr18 - 12358864 12358864 12358864 TGCTCTACACCATCAGAAGAGGGCCTGCTGGCATTGGCCGGACAGGCCGAGGGATGGGCGGACTC TGCTCTACACCATCAGAAGAGGGCCTGCTGGCGTTGGCCGGACAGGCCGAGGGATGGGCGGACTC T C AFG3L2 Ensembl:ENSG00000141385 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:12358813..12359947 32194978 MeRIP-seq:(Medium) rs1381207077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51752,Human_RBP_ID_238490 Human_Splice_Rec_1895724,Human_Splice_Rec_1895752,Human_Splice_Rec_1895754 RMVar_hsa_circ_123567,RMVar_hsa_circ_107465,RMVar_hsa_circ_188692,RMVar_hsa_circ_188693,RMVar_hsa_circ_344321,RMVar_hsa_circ_29644,RMVar_hsa_circ_16633,RMVar_hsa_circ_40394,RMVar_hsa_circ_946,RMVar_hsa_circ_33127,RMVar_hsa_circ_116357,RMVar_hsa_circ_343859,RMVar_hsa_circ_92799,RMVar_hsa_circ_188697,RMVar_hsa_circ_11484,RMVar_hsa_circ_188698,RMVar_hsa_circ_328229,RMVar_hsa_circ_343094,RMVar_hsa_circ_22203,RMVar_hsa_circ_374014,RMVar_hsa_circ_328051,RMVar_hsa_circ_348254,RMVar_hsa_circ_188700,RMVar_hsa_circ_347712,RMVar_hsa_circ_39336,RMVar_hsa_circ_188706,RMVar_hsa_circ_42158,RMVar_hsa_circ_188701,RMVar_hsa_circ_338507,RMVar_hsa_circ_367937,RMVar_hsa_circ_358776,RMVar_hsa_circ_110887,RMVar_hsa_circ_282763,RMVar_hsa_circ_302398,RMVar_hsa_circ_377643,RMVar_hsa_circ_289156,RMVar_hsa_circ_271596,RMVar_hsa_circ_188707,RMVar_hsa_circ_188709,RMVar_hsa_circ_188710,RMVar_hsa_circ_188708,RMVar_hsa_circ_270448,RMVar_hsa_circ_341592,RMVar_hsa_circ_64743,RMVar_hsa_circ_188711,RMVar_hsa_circ_188712 69312 RMVar_ID_69312 Human_SNP_ID_638264862 m1A Human chr18 - 12367309 12367309 12367309 GGTGGTGGCGGTGGAAAACGAGGTGGCAAGAAAGATGATTCTCACTGGTGGTCCAGGTTTCAGAA GGTGGTGGCGGTGGAAAACGAGGTGGCAAGAAGGATGATTCTCACTGGTGGTCCAGGTTTCAGAA T C AFG3L2 Ensembl:ENSG00000141385 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:12367100..12367358 32194978 MeRIP-seq:(Medium) rs757645715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27814513 Human_Splice_Rec_1895716,Human_Splice_Rec_1895717 RMVar_hsa_circ_123567,RMVar_hsa_circ_188692,RMVar_hsa_circ_344321,RMVar_hsa_circ_40394,RMVar_hsa_circ_92799,RMVar_hsa_circ_11484,RMVar_hsa_circ_188698,RMVar_hsa_circ_343094,RMVar_hsa_circ_22203,RMVar_hsa_circ_347712,RMVar_hsa_circ_42158,RMVar_hsa_circ_367937,RMVar_hsa_circ_110887,RMVar_hsa_circ_302398,RMVar_hsa_circ_377643,RMVar_hsa_circ_188709,RMVar_hsa_circ_188710,RMVar_hsa_circ_341592,RMVar_hsa_circ_188712,RMVar_hsa_circ_52513,RMVar_hsa_circ_292719,RMVar_hsa_circ_188714,RMVar_hsa_circ_322596,RMVar_hsa_circ_342358,RMVar_hsa_circ_275860 69313 RMVar_ID_69313 Human_SNP_ID_638267766 m1A Human chr18 + 12377139 12377139 12377139 CCGGGACGCTGCGCAGGCGCGGGCAGGCGACGACTGGCGGCCTCGGGAAGCGGGCTCGGCTCGGG CCGGGACGCTGCGCAGGCGCGGGCAGGCGACGGCTGGCGGCCTCGGGAAGCGGGCTCGGCTCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12377088..12377243 26863196 MeRIP-seq:(Medium) rs1012146602 Functional Loss SNV dbSNP153 33..33 33 - - - 69314 RMVar_ID_69314 Human_SNP_ID_638267822 m1A Human chr18 + 12377215 12377215 12377215 AGGCAGCGAAGCGCGCCGGCGGCTCACGGAGGAGCCCAAGCTCTCAACGCGGCGTCTCCTGCCGC AGGCAGCGAAGCGCGCCGGCGGCTCACGGAGGGGCCCAAGCTCTCAACGCGGCGTCTCCTGCCGC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr18:12377114..12377214 26863410 MeRIP-seq:(Medium) rs1458086085 Functional Loss SNV dbSNP153 33..33 33 - - - 69315 RMVar_ID_69315 Human_SNP_ID_638276152 m1A Human chr18 - 12408009 12408009 12408009 GACGGCCCCACCGCGGCCCTCAGCCCGGCCTCACCCAAACACGTGCTCCGAGCTCCAGATCTTCA GACGGCCCCACCGCGGCCCTCAGCCCGGCCTCGCCCAAACACGTGCTCCGAGCTCCAGATCTTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:12407972..12408122 26863196 MeRIP-seq:(Medium) rs1180259649 Functional Loss SNV dbSNP153 33..33 33 - - - 69316 RMVar_ID_69316 Human_SNP_ID_638276157 m1A Human chr18 + 12408022 12408022 12408022 CTCGGAGCACGTGTTTGGGTGAGGCCGGGCTGAGGGCCGCGGTGGGGCCGTCCAGACGCCGGCTC CTCGGAGCACGTGTTTGGGTGAGGCCGGGCTGGGGGCCGCGGTGGGGCCGTCCAGACGCCGGCTC A G PRELID3A Ensembl:ENSG00000141391 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:12407977..12408286 26863196 MeRIP-seq:(Medium) rs985303290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19087947 69317 RMVar_ID_69317 Human_SNP_ID_638276280 m1A Human chr18 + 12408308 12408293 12408308 TGGTGGTCGACAGCCAGGGCGGGGGCAGCCGGAGCGGGGGCGGCCGGGGCGGGGGCGGCCGGAGC TGGTGGTCGACAGCCAGG_______________GCGGGGGCGGCCGGGGCGGGGGCGGCCGGAGC GGCGGGGGCAGCCGGA G PRELID3A Ensembl:ENSG00000141391 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:12408294..12408436 26863196 MeRIP-seq:(Medium) rs1187717958 Functional Loss DEL dbSNP153 19..33 33 - - - 69318 RMVar_ID_69318 Human_SNP_ID_638276291 m1A Human chr18 + 12408308 12408308 12408308 TGGTGGTCGACAGCCAGGGCGGGGGCAGCCGGAGCGGGGGCGGCCGGGGCGGGGGCGGCCGGAGC TGGTGGTCGACAGCCAGGGCGGGGGCAGCCGGGGCGGGGGCGGCCGGGGCGGGGGCGGCCGGAGC A G PRELID3A Ensembl:ENSG00000141391 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:12408294..12408436 26863196 MeRIP-seq:(Medium) rs1238439663 Functional Loss SNV dbSNP153 33..33 33 - - - 69319 RMVar_ID_69319 Human_SNP_ID_638276342 m1A Human chr18 - 12408417 12408417 12408417 GGAAGGTTTATGACAATCTCAGCAAAGGCGCCAGCTTGCAGGCCTCTCCCCTGCCCTGCTCCCGA GGAAGGTTTATGACAATCTCAGCAAAGGCGCCGGCTTGCAGGCCTCTCCCCTGCCCTGCTCCCGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:12408369..12408623 26863196 MeRIP-seq:(Medium) rs1342015798 Functional Loss SNV dbSNP153 33..33 33 - - - 69320 RMVar_ID_69320 Human_SNP_ID_638279057 m1A Human chr18 - 12418936 12418936 12418936 AATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGAATTATGGGCATGAGCCACCGCACTCAGCCTCC AATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATTATGGGCATGAGCCACCGCACTCAGCCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12418933..12419068 26863196 MeRIP-seq:(Medium) rs1189469188 Functional Loss SNV dbSNP153 33..33 33 - - - 69321 RMVar_ID_69321 Human_SNP_ID_638282851 m1A Human chr18 - 12431648 12431648 12431648 AAAGCCATGGCCCCAGGCCCCGTGAGCCCCGCAGTCAGAGCCCACCGAGGCCAGCAGCAGATGTG AAAGCCATGGCCCCAGGCCCCGTGAGCCCCGCCGTCAGAGCCCACCGAGGCCAGCAGCAGATGTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:12431603..12431713 32194978 MeRIP-seq:(Medium) rs778256838 Functional Loss SNV dbSNP153 33..33 33 - - - 69322 RMVar_ID_69322 Human_SNP_ID_638322649 m1A Human chr18 - 12596885 12596885 12596885 GTGAAGGAGGAAACAGGAAGGGGGTTAGCAGGACAGTGCAGGGCTATAGCTGTGGTATTAAGTTC GTGAAGGAGGAAACAGGAAGGGGGTTAGCAGGGCAGTGCAGGGCTATAGCTGTGGTATTAAGTTC T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12596883..12596992 26863196 MeRIP-seq:(Medium) rs1318308485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6667900 RMVar_hsa_circ_27694,RMVar_hsa_circ_39094,RMVar_hsa_circ_323244,RMVar_hsa_circ_25748,RMVar_hsa_circ_188745,RMVar_hsa_circ_293988,RMVar_hsa_circ_329291,RMVar_hsa_circ_188747 69323 RMVar_ID_69323 Human_SNP_ID_638325765 m1A Human chr18 - 12610014 12610014 12610014 GCATCAGTGAGGAGCAAGAAGGACCTCCTCCCAGTTCCAGGTTCAGCAACCTGATAACTGTGACA GCATCAGTGAGGAGCAAGAAGGACCTCCTCCCGGTTCCAGGTTCAGCAACCTGATAACTGTGACA T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12610012..12610236 26863196 MeRIP-seq:(Medium) rs1173018815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27694,RMVar_hsa_circ_39094,RMVar_hsa_circ_323244,RMVar_hsa_circ_25748,RMVar_hsa_circ_188745,RMVar_hsa_circ_293988,RMVar_hsa_circ_329291,RMVar_hsa_circ_188747 69324 RMVar_ID_69324 Human_SNP_ID_638325882 m1A Human chr18 - 12610593 12610593 12610593 TTTACTCTAGCCACATTCAGCTATACAAATGCAGGTGGGGAGGCAGTGAAGAGGTAGATTTAACC TTTACTCTAGCCACATTCAGCTATACAAATGCGGGTGGGGAGGCAGTGAAGAGGTAGATTTAACC T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12610582..12611231 26863196 MeRIP-seq:(Medium) rs1485182330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27694,RMVar_hsa_circ_39094,RMVar_hsa_circ_323244,RMVar_hsa_circ_25748,RMVar_hsa_circ_188745,RMVar_hsa_circ_293988,RMVar_hsa_circ_329291,RMVar_hsa_circ_188747 69325 RMVar_ID_69325 Human_SNP_ID_638332463 m1A Human chr18 - 12635092 12635092 12635092 AAAGTAATCCTTTTCATTTTTATTACAGGTAAATTGGGATATTCACAATGTATGGAAACAGAGGT AAAGTAATCCTTTTCATTTTTATTACAGGTAAGTTGGGATATTCACAATGTATGGAAACAGAGGT T C SPIRE1 Ensembl:ENSG00000134278 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12635080..12635167 26863196 MeRIP-seq:(Medium) rs904300020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8468335 Human_Splice_Rec_1895854,Human_Splice_Rec_1895855,Human_Splice_Rec_1895886,Human_Splice_Rec_1895887,Human_Splice_Rec_1895915,Human_Splice_Rec_1895942,Human_Splice_Rec_1895943,Human_Splice_Rec_1895971,Human_Splice_Rec_1896052,Human_Splice_Rec_1896053,Human_Splice_Rec_1896062,Human_Splice_Rec_1896063,Human_Splice_Rec_1896070,Human_Splice_Rec_1896071 RMVar_hsa_circ_27694,RMVar_hsa_circ_39094,RMVar_hsa_circ_323244,RMVar_hsa_circ_25748,RMVar_hsa_circ_188745,RMVar_hsa_circ_293988,RMVar_hsa_circ_329291,RMVar_hsa_circ_188747 69326 RMVar_ID_69326 Human_SNP_ID_638338593 m1A Human chr18 - 12658669 12658662 12658669 TCACGGGAAACTGCCGGAGGCTTTCAGGGCCCAGGGCCCGGCGGGGAGGCTTCAGCGGGCCTGCA TCACGGGAAACTGCCGGAGGCTTTCAGGGCCC_______GGCGGGGAGGCTTCAGCGGGCCTGCA CGGGCCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12658618..12658740 26863196 MeRIP-seq:(Medium) rs1174118766 Functional Loss DEL dbSNP153 33..39 33 - - - 69327 RMVar_ID_69327 Human_SNP_ID_638350628 m1A Human chr18 + 12703068 12703068 12703068 GCTTCCGCCTTCTTGCTGCCCTCGTTCTTGCCAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCAC GCTTCCGCCTTCTTGCTGCCCTCGTTCTTGCCGGGGCCGCGGTTAGTCCCTGCTGGCCACCCCAC A G PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12703026..12703150 26863196 MeRIP-seq:(Medium) rs3809916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4482729,Human_RBP_ID_5319528,Human_RBP_ID_9327722,Human_RBP_ID_17381596,Human_RBP_ID_17497563 Human_Splice_Rec_1896109,Human_Splice_Rec_1896119,Human_Splice_Rec_1896127 Human_miRNA_ID_2346517 GWAS_ID_8348,GWAS_ID_8349,GWAS_ID_8350,GWAS_ID_8351,GWAS_ID_8352,GWAS_ID_8353,GWAS_ID_8354,GWAS_ID_8355,GWAS_ID_8356,GWAS_ID_8357,GWAS_ID_8358,GWAS_ID_8359,GWAS_ID_8360,GWAS_ID_8361,GWAS_ID_8362,GWAS_ID_8363,GWAS_ID_8364,GWAS_ID_8365,GWAS_ID_8366,GWAS_ID_8367,GWAS_ID_8368,GWAS_ID_8369,GWAS_ID_8370,GWAS_ID_8371,GWAS_ID_8372,GWAS_ID_8373,GWAS_ID_8374,GWAS_ID_8375,GWAS_ID_8376,GWAS_ID_8377,GWAS_ID_8378 RMVar_hsa_circ_78226,RMVar_hsa_circ_188748,RMVar_hsa_circ_101036,RMVar_hsa_circ_188758 69328 RMVar_ID_69328 Human_SNP_ID_638350664 m1A Human chr18 + 12703099 12703099 12703099 CAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCACTGCGACCATGTTCGTTCCCTGCGGGGAGTCG CAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCCCTGCGACCATGTTCGTTCCCTGCGGGGAGTCG A C PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12703050..12703149 26863196 MeRIP-seq:(Medium) rs1436178296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504825,Human_RBP_ID_4494148,Human_RBP_ID_5319528,Human_RBP_ID_5442219,Human_RBP_ID_9327722,Human_RBP_ID_17381596,Human_RBP_ID_17497563 Human_Splice_Rec_1896109,Human_Splice_Rec_1896119,Human_Splice_Rec_1896127 RMVar_hsa_circ_78226,RMVar_hsa_circ_188748,RMVar_hsa_circ_101036,RMVar_hsa_circ_188758 69329 RMVar_ID_69329 Human_SNP_ID_638350665 m1A Human chr18 + 12703099 12703099 12703099 CAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCACTGCGACCATGTTCGTTCCCTGCGGGGAGTCG CAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCGCTGCGACCATGTTCGTTCCCTGCGGGGAGTCG A G PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12703050..12703149 26863196 MeRIP-seq:(Medium) rs1436178296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504825,Human_RBP_ID_4494148,Human_RBP_ID_5319528,Human_RBP_ID_5442219,Human_RBP_ID_9327722,Human_RBP_ID_17381596,Human_RBP_ID_17497563 Human_Splice_Rec_1896109,Human_Splice_Rec_1896119,Human_Splice_Rec_1896127 RMVar_hsa_circ_78226,RMVar_hsa_circ_188748,RMVar_hsa_circ_101036,RMVar_hsa_circ_188758 69330 RMVar_ID_69330 Human_SNP_ID_638350672 m1A Human chr18 - 12703109 12703109 12703109 GGTCGGGGGCCGACTCCCCGCAGGGAACGAACATGGTCGCAGTGGGGTGGCCAGCAGGGACTAAC GGTCGGGGGCCGACTCCCCGCAGGGAACGAACGTGGTCGCAGTGGGGTGGCCAGCAGGGACTAAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:12703042..12703132 26863410 MeRIP-seq:(Medium) rs954365638 Functional Loss SNV dbSNP153 33..33 33 - - - 69331 RMVar_ID_69331 Human_SNP_ID_638400513 m1A Human chr18 + 12884155 12884155 12884155 GCTCGATGGTGGTGGGCATGGCTGCGGGAGCGAGCTGGCGCGAGCAGAGCCTGCGCCGGCGGAGA GCTCGATGGTGGTGGGCATGGCTGCGGGAGCGCGCTGGCGCGAGCAGAGCCTGCGCCGGCGGAGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12884022..12884155 26863196 MeRIP-seq:(Medium) rs1194443660 Functional Loss SNV dbSNP153 33..33 33 - - - 69332 RMVar_ID_69332 Human_SNP_ID_638400523 m1A Human chr18 + 12884165 12884165 12884165 GGTGGGCATGGCTGCGGGAGCGAGCTGGCGCGAGCAGAGCCTGCGCCGGCGGAGAGGCTCAGGCC GGTGGGCATGGCTGCGGGAGCGAGCTGGCGCGGGCAGAGCCTGCGCCGGCGGAGAGGCTCAGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12884004..12884186 26863196 MeRIP-seq:(Medium) rs1265405213 Functional Loss SNV dbSNP153 33..33 33 - - - 69333 RMVar_ID_69333 Human_SNP_ID_638417100 m1A Human chr18 - 12948076 12948064 12948076 CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCAGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGC____________GCGTGGCCCGTAGCCTAGCCA CGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:12948026..12948162;chr18:12946928..12948100 26863196 MeRIP-seq:(Medium) rs898434963 Functional Loss DEL dbSNP153 33..44 33 - - - 69334 RMVar_ID_69334 Human_SNP_ID_638417102 m1A Human chr18 - 12948076 12948067 12948076 CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCAGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGC_________GGCGCGTGGCCCGTAGCCTAGCCA CGCCGCCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:12948026..12948162;chr18:12946928..12948100 26863196 MeRIP-seq:(Medium) rs878916207 Functional Loss DEL dbSNP153 33..41 33 - - - 69335 RMVar_ID_69335 Human_SNP_ID_638417106 m1A Human chr18 - 12948076 12948070 12948076 CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCAGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGC______GGCGGCGCGTGGCCCGTAGCCTAGCCA CGCCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:12948026..12948162;chr18:12946928..12948100 26863196 MeRIP-seq:(Medium) rs1002108473 Functional Loss DEL dbSNP153 33..38 33 - - - 69336 RMVar_ID_69336 Human_SNP_ID_638417113 m1A Human chr18 - 12948076 12948076 12948076 CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCAGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCGGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:12948026..12948162;chr18:12946928..12948100 26863196 MeRIP-seq:(Medium) rs960331800 Functional Loss SNV dbSNP153 33..33 33 - - - 69337 RMVar_ID_69337 Human_SNP_ID_638417138 m1A Human chr18 - 12948126 12948126 12948126 CCTTGTGGTCCGCCGCGATGCTGCGAGCCACAAACATGGTTTCCGTCGGGCCCGCGCCTCCGAAG CCTTGTGGTCCGCCGCGATGCTGCGAGCCACAGACATGGTTTCCGTCGGGCCCGCGCCTCCGAAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:12948026..12948180 26863410 MeRIP-seq:(Medium) rs1394599211 Functional Loss SNV dbSNP153 33..33 33 - - - 69338 RMVar_ID_69338 Human_SNP_ID_638429050 m1A Human chr18 - 12991539 12991539 12991539 CCGCCCCACAGCCTGCGCCCCCACCCGGCCCAACCGTCACTGTCCCGTCGGTCCGGCAGCCGAAA CCGCCCCACAGCCTGCGCCCCCACCCGGCCCAGCCGTCACTGTCCCGTCGGTCCGGCAGCCGAAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:12991518..12991661 26863196 MeRIP-seq:(Medium) rs982572117 Functional Loss SNV dbSNP153 33..33 33 - - - 69339 RMVar_ID_69339 Human_SNP_ID_638430063 m1A Human chr18 - 12995927 12995927 12995927 CCTCTACTCTTCTCCCTTGCTCACTCCATTCCAGTCATCCTAACCTCCCTGCTGTTCCTGAAACA CCTCTACTCTTCTCCCTTGCTCACTCCATTCCTGTCATCCTAACCTCCCTGCTGTTCCTGAAACA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:12995758..12995962 26863196 MeRIP-seq:(Medium) rs763624652 Functional Loss SNV dbSNP153 33..33 33 - - - 69340 RMVar_ID_69340 Human_SNP_ID_638430064 m1A Human chr18 - 12995927 12995927 12995927 CCTCTACTCTTCTCCCTTGCTCACTCCATTCCAGTCATCCTAACCTCCCTGCTGTTCCTGAAACA CCTCTACTCTTCTCCCTTGCTCACTCCATTCCCGTCATCCTAACCTCCCTGCTGTTCCTGAAACA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:12995758..12995962 26863196 MeRIP-seq:(Medium) rs763624652 Functional Loss SNV dbSNP153 33..33 33 - - - 69341 RMVar_ID_69341 Human_SNP_ID_638456311 m1A Human chr18 + 13100451 13100451 13100451 TTGGTCAAACCAATGACAAAACCGCCTTCCACAAAAGTTGAAATAAGAAACAAGAGTATTACTTT TTGGTCAAACCAATGACAAAACCGCCTTCCACGAAAGTTGAAATAAGAAACAAGAGTATTACTTT A G CEP192 Ensembl:ENSG00000101639 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs758146649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1896679,Human_Splice_Rec_1896765,Human_Splice_Rec_1896849,Human_Splice_Rec_1896917,Human_Splice_Rec_1896987,Human_Splice_Rec_1897037,Human_Splice_Rec_1897081,Human_Splice_Rec_1897127 RMVar_hsa_circ_323198,RMVar_hsa_circ_310902,RMVar_hsa_circ_37529,RMVar_hsa_circ_274052,RMVar_hsa_circ_29463,RMVar_hsa_circ_35218,RMVar_hsa_circ_334497,RMVar_hsa_circ_349383,RMVar_hsa_circ_26020,RMVar_hsa_circ_188828,RMVar_hsa_circ_9134,RMVar_hsa_circ_102490,RMVar_hsa_circ_188838,RMVar_hsa_circ_271826,RMVar_hsa_circ_188839,RMVar_hsa_circ_45170,RMVar_hsa_circ_69074,RMVar_hsa_circ_297152,RMVar_hsa_circ_188851,RMVar_hsa_circ_318824,RMVar_hsa_circ_188847,RMVar_hsa_circ_371290,RMVar_hsa_circ_353364,RMVar_hsa_circ_188850,RMVar_hsa_circ_48285,RMVar_hsa_circ_32160,RMVar_hsa_circ_188853,RMVar_hsa_circ_99811,RMVar_hsa_circ_286143,RMVar_hsa_circ_188852,RMVar_hsa_circ_188854,RMVar_hsa_circ_188856,RMVar_hsa_circ_279973,RMVar_hsa_circ_302266,RMVar_hsa_circ_188855,RMVar_hsa_circ_43936 69342 RMVar_ID_69342 Human_SNP_ID_638460095 m1A Human chr18 + 13115727 13115727 13115727 GCTCCCAGATACCATTCAGCAAACACAAGTGGAGGATCAGGTTTGAGGACAAAAATCACAAGTTC GCTCCCAGATACCATTCAGCAAACACAAGTGGGGGATCAGGTTTGAGGACAAAAATCACAAGTTC A G CEP192 Ensembl:ENSG00000101639 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:13115719..13115906 26863196 MeRIP-seq:(Medium) rs1193801302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13252516 RMVar_hsa_circ_274052,RMVar_hsa_circ_29463,RMVar_hsa_circ_15304,RMVar_hsa_circ_334497,RMVar_hsa_circ_188828,RMVar_hsa_circ_45170,RMVar_hsa_circ_69074,RMVar_hsa_circ_188851,RMVar_hsa_circ_318824,RMVar_hsa_circ_188847,RMVar_hsa_circ_99811,RMVar_hsa_circ_188852,RMVar_hsa_circ_188856,RMVar_hsa_circ_300824,RMVar_hsa_circ_188857,RMVar_hsa_circ_339953,RMVar_hsa_circ_39935,RMVar_hsa_circ_188859,RMVar_hsa_circ_316081 69343 RMVar_ID_69343 Human_SNP_ID_638600736 m1A Human chr18 - 13682107 13682107 13682107 ATTACCTAATTTTTTTGAAAAATTGTCTTTGTAGAAGCTGAAACCTATCAACACTCTTCAAAATG ATTACCTAATTTTTTTGAAAAATTGTCTTTGTGGAAGCTGAAACCTATCAACACTCTTCAAAATG T C FAM210A Ensembl:ENSG00000177150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:13682060..13697561 26863196 MeRIP-seq:(Medium) rs1330223601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494155 RMVar_hsa_circ_188883,RMVar_hsa_circ_188890,RMVar_hsa_circ_52044,RMVar_hsa_circ_188892,RMVar_hsa_circ_330025 69344 RMVar_ID_69344 Human_SNP_ID_638611545 m1A Human chr18 + 13726398 13726398 13726398 CGCGCAGGCTGGACCACAGCTCCTCGGATGCCACGGCGGTGTCACTCAGCAGAGCAGCCCGACAA CGCGCAGGCTGGACCACAGCTCCTCGGATGCCGCGGCGGTGTCACTCAGCAGAGCAGCCCGACAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:13726351..13726505 26863196 MeRIP-seq:(Medium) rs1413195866 Functional Loss SNV dbSNP153 33..33 33 - - - 69345 RMVar_ID_69345 Human_SNP_ID_40764292 m1A Human chr1 + 180154923 180154922 180154923 TGAGCGCAGCGCCGAGGATGAGGAGGTGCAACAGCGGCTCCGGGCCGCCGCCGTCGCTGCTGCTG TGAGCGCAGCGCCGAGGATGAGGAGGTGCAAC_GCGGCTCCGGGCCGCCGCCGTCGCTGCTGCTG CA C QSOX1 Ensembl:ENSG00000116260 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:180154876..180155055;chr1:180154876..180155091 26863196 MeRIP-seq:(Medium) rs1174977370 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_858899,Human_RBP_ID_4073188,Human_RBP_ID_22428731 RMVar_hsa_circ_138082,RMVar_hsa_circ_126955 69346 RMVar_ID_69346 Human_SNP_ID_40773577 m1A Human chr1 + 180191275 180191275 180191275 CTCTTGGTGGACCTCTAGTGTGAGGCAGGGGGACAGAGAGGCCTGCAGTGCATCAGGGCTAGGGC CTCTTGGTGGACCTCTAGTGTGAGGCAGGGGGGCAGAGAGGCCTGCAGTGCATCAGGGCTAGGGC A G QSOX1 Ensembl:ENSG00000116260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180191267..180191552 26863196 MeRIP-seq:(Medium) rs1473682599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801966 RMVar_hsa_circ_10473,RMVar_hsa_circ_86078,RMVar_hsa_circ_138088,RMVar_hsa_circ_138089,RMVar_hsa_circ_95713,RMVar_hsa_circ_78194,RMVar_hsa_circ_109016,RMVar_hsa_circ_108105,RMVar_hsa_circ_138091,RMVar_hsa_circ_85642,RMVar_hsa_circ_138092,RMVar_hsa_circ_138094,RMVar_hsa_circ_65866,RMVar_hsa_circ_138095 69347 RMVar_ID_69347 Human_SNP_ID_40774155 m1A Human chr1 - 180193455 180193455 180193455 AATCTCCTGCTTTTACCCCTCCACGCAGCAGGACGTTGGCACCCTACTCTCCTCACTCCTGGCAA AATCTCCTGCTTTTACCCCTCCACGCAGCAGGGCGTTGGCACCCTACTCTCCTCACTCCTGGCAA T C lnc-ACBD6-2 RNACentral:URS00008B7F40 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:180193449..180193537 26863196 MeRIP-seq:(Medium) rs957366928 Functional Loss SNV dbSNP153 33..33 33 - - - 69348 RMVar_ID_69348 Human_SNP_ID_40775113 m1A Human chr1 - 180196382 180196382 180196382 TGATGTTGCTTGGGGAGAAGTGGGCCTTGAGGAAGTTGAGGGTGGCTTCCACGTCCCACACGGGC TGATGTTGCTTGGGGAGAAGTGGGCCTTGAGGCAGTTGAGGGTGGCTTCCACGTCCCACACGGGC T G lnc-ACBD6-2 RNACentral:URS00008B7F40 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:180196333..180196733 26863196 MeRIP-seq:(Medium) rs1444520490 Functional Loss SNV dbSNP153 33..33 33 - - - 69349 RMVar_ID_69349 Human_SNP_ID_40775572 m1A Human chr1 - 180197645 180197645 180197645 CACCCTACAGCCCAGCAACCATGGCTTGCCTCACCTGGGAGACCAGCACGACTTCCAGAAGCTTC CACCCTACAGCCCAGCAACCATGGCTTGCCTCCCCTGGGAGACCAGCACGACTTCCAGAAGCTTC T G lnc-ACBD6-2 RNACentral:URS00008B7F40 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:180197594..180197765 26863196 MeRIP-seq:(Medium) rs907497026 Functional Loss SNV dbSNP153 33..33 33 - - - 69350 RMVar_ID_69350 Human_SNP_ID_40775576 m1A Human chr1 + 180197696 180197696 180197696 TGGGCTGTAGGGTGAGTGGCTTGCTTGGTGGGACCTGACGAGTTGGTGGCATGGGAAGGATGTGG TGGGCTGTAGGGTGAGTGGCTTGCTTGGTGGGGCCTGACGAGTTGGTGGCATGGGAAGGATGTGG A G QSOX1 Ensembl:ENSG00000116260 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:180197601..180197750 26863196 MeRIP-seq:(Medium) rs530453229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334756,Human_RBP_ID_803048,Human_RBP_ID_4073192,Human_RBP_ID_9352404,Human_RBP_ID_10680495,Human_RBP_ID_17647202,Human_RBP_ID_23349172,Human_RBP_ID_26388945 RMVar_hsa_circ_86078,RMVar_hsa_circ_138088,RMVar_hsa_circ_138089,RMVar_hsa_circ_95713,RMVar_hsa_circ_78194,RMVar_hsa_circ_109016,RMVar_hsa_circ_108105,RMVar_hsa_circ_138091,RMVar_hsa_circ_85642,RMVar_hsa_circ_138092,RMVar_hsa_circ_138094,RMVar_hsa_circ_138095 69351 RMVar_ID_69351 Human_SNP_ID_40775772 m1A Human chr1 + 180198305 180198305 180198305 TCCTGCCTCAGTGCCCTGGGCTGGTGAGGGAGAAGCCTGTCTGCACCTGCCTAATTCCAGCTCCT TCCTGCCTCAGTGCCCTGGGCTGGTGAGGGAGGAGCCTGTCTGCACCTGCCTAATTCCAGCTCCT A G QSOX1 Ensembl:ENSG00000116260 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:180198254..180198354 32194978 MeRIP-seq:(Medium) rs3843273 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8379,GWAS_ID_8380,GWAS_ID_8381 69352 RMVar_ID_69352 Human_SNP_ID_40788470 m1A Human chr1 - 180249906 180249906 180249906 TCACCCACACACACTCTCACACACACTGTCACACACACACTCATACACACACTCACACACGCACA TCACCCACACACACTCTCACACACACTGTCACGCACACACTCATACACACACTCACACACGCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180249900..180250033 26863196 MeRIP-seq:(Medium) rs1029670424 Functional Loss SNV dbSNP153 33..33 33 - - - 69353 RMVar_ID_69353 Human_SNP_ID_40791253 m1A Human chr1 + 180259785 180259782 180259786 CGCCCTGGGGTCTGCTGGGTAAGGAAGGAGGGAAGCGAGGGACAGTGACAAGCCCAAGGGGAAGG CGCCCTGGGGTCTGCTGGGTAAGGAAGGAG____GCGAGGGACAGTGACAAGCCCAAGGGGAAGG GGGAA G LHX4 Ensembl:ENSG00000121454 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180259672..180259920 26863196 MeRIP-seq:(Medium) rs1301738768 Functional Loss DEL dbSNP153 31..34 33 - - - 69354 RMVar_ID_69354 Human_SNP_ID_40791314 m1A Human chr1 - 180260017 180260017 180260017 CACCCTTGGTGACTGCAGTCCCCACATAGACCATCCTTCCAGGCCCTCCCTCTCAATTCTTTGAC CACCCTTGGTGACTGCAGTCCCCACATAGACCGTCCTTCCAGGCCCTCCCTCTCAATTCTTTGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:180260007..180260222;chr1:180260010..180260171 26863196 MeRIP-seq:(Medium) rs935940384 Functional Loss SNV dbSNP153 33..33 33 - - - 69355 RMVar_ID_69355 Human_SNP_ID_40794938 m1A Human chr1 + 180274255 180274255 180274255 ATTTATGGCAACGTGGGGGACGTTACAGGCGGACAGTTAATGAATGGGAGCTTCTCCATGGACGG ATTTATGGCAACGTGGGGGACGTTACAGGCGGCCAGTTAATGAATGGGAGCTTCTCCATGGACGG A C LHX4 Ensembl:ENSG00000121454 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180274170..180274295 26863196 MeRIP-seq:(Medium) rs373879455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_162900 69356 RMVar_ID_69356 Human_SNP_ID_40798397 m1A Human chr1 - 180288350 180288350 180288350 ACACAACTGGCAAGGCTTAATCAAAAGACTGGAAAACTGCAGTCTGTAATAGCATAAGGCTTCCA ACACAACTGGCAAGGCTTAATCAAAAGACTGGGAAACTGCAGTCTGTAATAGCATAAGGCTTCCA T C ACBD6 Ensembl:ENSG00000230124 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:180288301..180326520 32194978 MeRIP-seq:(Medium) rs1048301405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334789,Human_RBP_ID_973296,Human_RBP_ID_1416646,Human_RBP_ID_1730818,Human_RBP_ID_8292010,Human_RBP_ID_8959535,Human_RBP_ID_18220762,Human_RBP_ID_27391771 Human_Splice_Rec_162931,Human_Splice_Rec_162955,Human_Splice_Rec_162975,Human_Splice_Rec_162987 RMVar_hsa_circ_60764,RMVar_hsa_circ_87926,RMVar_hsa_circ_274246,RMVar_hsa_circ_138097 69357 RMVar_ID_69357 Human_SNP_ID_40798425 m1A Human chr1 - 180288417 180288416 180288417 GACCAGGATGGCTGCCTGCCAGAGGAGGTGACAGGCTGCAAAACAGTTTCTTTGGTGCTGCAGCG GACCAGGATGGCTGCCTGCCAGAGGAGGTGAC_GGCTGCAAAACAGTTTCTTTGGTGCTGCAGCG CT C ACBD6 Ensembl:ENSG00000230124 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:180288366..180288525 26863196 MeRIP-seq:(Medium) rs1188011782 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_334793,Human_RBP_ID_855574,Human_RBP_ID_17732763,Human_RBP_ID_18966259,Human_RBP_ID_23349278,Human_RBP_ID_26799235 Human_miRNA_ID_2224776,Human_miRNA_ID_2646694,Human_miRNA_ID_2669287,Human_miRNA_ID_3099935 RMVar_hsa_circ_60764,RMVar_hsa_circ_87926,RMVar_hsa_circ_274246,RMVar_hsa_circ_138097 69358 RMVar_ID_69358 Human_SNP_ID_40819702 m1A Human chr1 - 180378806 180378806 180378806 GTGGCTGTGATGGGTGGAGTGGGCCAGTGCCCAAATCTGCAGGTAGCACATGCTGGGGGGTGCCA GTGGCTGTGATGGGTGGAGTGGGCCAGTGCCCGAATCTGCAGGTAGCACATGCTGGGGGGTGCCA T C ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:180378804..180378876 26863196 MeRIP-seq:(Medium) rs1416140879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1551,Human_RBP_ID_800721,Human_RBP_ID_17099691,Human_RBP_ID_27835350 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_56484,RMVar_hsa_circ_90937,RMVar_hsa_circ_138098 69359 RMVar_ID_69359 Human_SNP_ID_40824225 m1A Human chr1 - 180397607 180397607 180397607 AGATAACAAATTCATTTATCTTCTGTGTTTTTAGGGTAGGGCTCTACTTCACTGGGCCTGTGATC AGATAACAAATTCATTTATCTTCTGTGTTTTTTGGGTAGGGCTCTACTTCACTGGGCCTGTGATC T A ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:180397572..180413432 32194978 MeRIP-seq:(Medium) rs765369140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23944,Human_RBP_ID_973299,Human_RBP_ID_2109700,Human_RBP_ID_18557564,Human_RBP_ID_18969378,Human_RBP_ID_26312290 Human_Splice_Rec_162925,Human_Splice_Rec_162951,Human_Splice_Rec_162971,Human_Splice_Rec_162981,Human_Splice_Rec_162999 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_56484,RMVar_hsa_circ_90937,RMVar_hsa_circ_281863,RMVar_hsa_circ_377578,RMVar_hsa_circ_138098,RMVar_hsa_circ_298940,RMVar_hsa_circ_277140,RMVar_hsa_circ_138100,RMVar_hsa_circ_138102,RMVar_hsa_circ_138103,RMVar_hsa_circ_138101 69360 RMVar_ID_69360 Human_SNP_ID_40824226 m1A Human chr1 - 180397607 180397607 180397607 AGATAACAAATTCATTTATCTTCTGTGTTTTTAGGGTAGGGCTCTACTTCACTGGGCCTGTGATC AGATAACAAATTCATTTATCTTCTGTGTTTTTGGGGTAGGGCTCTACTTCACTGGGCCTGTGATC T C ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:180397572..180413432 32194978 MeRIP-seq:(Medium) rs765369140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23944,Human_RBP_ID_973299,Human_RBP_ID_2109700,Human_RBP_ID_18557564,Human_RBP_ID_18969378,Human_RBP_ID_26312290 Human_Splice_Rec_162925,Human_Splice_Rec_162951,Human_Splice_Rec_162971,Human_Splice_Rec_162981,Human_Splice_Rec_162999 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_56484,RMVar_hsa_circ_90937,RMVar_hsa_circ_281863,RMVar_hsa_circ_377578,RMVar_hsa_circ_138098,RMVar_hsa_circ_298940,RMVar_hsa_circ_277140,RMVar_hsa_circ_138100,RMVar_hsa_circ_138102,RMVar_hsa_circ_138103,RMVar_hsa_circ_138101 69361 RMVar_ID_69361 Human_SNP_ID_40833263 m1A Human chr1 + 180436608 180436608 180436608 GGAGCTCCACCTATAAGCTTAGAAGTGTCTGTATGATTGTAATCACATGGTGACAACACTCAGAA GGAGCTCCACCTATAAGCTTAGAAGTGTCTGTCTGATTGTAATCACATGGTGACAACACTCAGAA A C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1241262401 Functional Loss SNV dbSNP153 33..33 33 - - - 69362 RMVar_ID_69362 Human_SNP_ID_40847285 m1A Human chr1 - 180495467 180495467 180495467 TAAACCAAGCTTCTTTGATTTTGAAGGAAAGCAAAAATGGTAAGAAATTCCTGGAATCTTTAATG TAAACCAAGCTTCTTTGATTTTGAAGGAAAGCGAAAATGGTAAGAAATTCCTGGAATCTTTAATG T C ACBD6 Ensembl:ENSG00000230124 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:180495451..180495525 32194978 MeRIP-seq:(Medium) rs779123354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26848157 Human_Splice_Rec_162916,Human_Splice_Rec_162917,Human_Splice_Rec_162942,Human_Splice_Rec_162943,Human_Splice_Rec_162990,Human_Splice_Rec_162991 Human_miRNA_ID_2003951 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_90937,RMVar_hsa_circ_138098,RMVar_hsa_circ_298940,RMVar_hsa_circ_138103,RMVar_hsa_circ_3476,RMVar_hsa_circ_368429 69363 RMVar_ID_69363 Human_SNP_ID_40849229 m1A Human chr1 - 180502624 180502600 180502625 CACGCCGCTGGCACGCACGCCGCCCCGCCCCCACGGCCCAGCGCCAGCCGCGCCCCGCGCTCGCA CACGCCGCTGGCACGCACGCCGCCCCGCCCC_________________________GCGCTCGCA CGGGGCGCGGCTGGCGCTGGGCCGTG C ACBD6 Ensembl:ENSG00000230124 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:180502526..180502775 26863410 MeRIP-seq:(Medium) rs1230965400 Functional Loss DEL dbSNP153 32..56 33 - - - RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_90937,RMVar_hsa_circ_138098 69364 RMVar_ID_69364 Human_SNP_ID_40849275 m1A Human chr1 + 180502701 180502701 180502701 GCCTGCTCTGCGCCGGCGGGGAAGCGCGGGCGACGCTACGCTGGACGTCCTTCCCTGCCGGAGGA GCCTGCTCTGCGCCGGCGGGGAAGCGCGGGCGGCGCTACGCTGGACGTCCTTCCCTGCCGGAGGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:180502601..180502855 26863410 MeRIP-seq:(Medium) rs773128515 Functional Loss SNV dbSNP153 33..33 33 - - - 69365 RMVar_ID_69365 Human_SNP_ID_40880535 m1A Human chr1 + 180632063 180632063 180632063 AGGAGGAAGATGGCGGGCGGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCG AGGAGGAAGATGGCGGGCGGGCTGCTCTGAAGGGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCG A G XPR1 Ensembl:ENSG00000143324 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:180632001..180632275;chr1:180632001..180682391 26863196 MeRIP-seq:(Medium) rs1476482508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25089,Human_RBP_ID_745036,Human_RBP_ID_3934342,Human_RBP_ID_4074633,Human_RBP_ID_18415688,Human_RBP_ID_26315081 69366 RMVar_ID_69366 Human_SNP_ID_40880547 m1A Human chr1 + 180632081 180632078 180632081 GGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCG GGGCTGCTCTGAAGAGACCTCGGCGGCGGC___GGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCG CGGA C XPR1 Ensembl:ENSG00000143324 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:180632026..180632168 26863196 MeRIP-seq:(Medium) rs377070854 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_25089,Human_RBP_ID_3934342,Human_RBP_ID_4073195,Human_RBP_ID_5137706,Human_RBP_ID_18415116,Human_RBP_ID_26315081 69367 RMVar_ID_69367 Human_SNP_ID_40880548 m1A Human chr1 + 180632081 180632081 180632081 GGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCG GGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGCGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCG A C XPR1 Ensembl:ENSG00000143324 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:180632026..180632168 26863196 MeRIP-seq:(Medium) rs1295981324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25089,Human_RBP_ID_3934342,Human_RBP_ID_4073195,Human_RBP_ID_5137706,Human_RBP_ID_18415116,Human_RBP_ID_26315081 69368 RMVar_ID_69368 Human_SNP_ID_40880560 m1A Human chr1 + 180632097 180632097 180632097 ACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCGGGGCCCATGTGGGGAG ACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCGGCGCCGCGCCGCGCCGGGGCCCATGTGGGGAG A G XPR1 Ensembl:ENSG00000143324 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:180632017..180632112 26863410 MeRIP-seq:(Medium) rs1000178099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073195,Human_RBP_ID_5136910,Human_RBP_ID_18415116,Human_RBP_ID_26315081 RMVar_hsa_circ_138104 69369 RMVar_ID_69369 Human_SNP_ID_40893296 m1A Human chr1 + 180682308 180682308 180682308 TGAAAAAGAACTGTTTAGCTTCAGATACATTCAGTATAAAGCTTACTCATGATTTCATATATTGT TGAAAAAGAACTGTTTAGCTTCAGATACATTCGGTATAAAGCTTACTCATGATTTCATATATTGT A G XPR1 Ensembl:ENSG00000143324 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:180682306..180682374 26863196 MeRIP-seq:(Medium) rs1253710338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22634711 RMVar_hsa_circ_138105 69370 RMVar_ID_69370 Human_SNP_ID_40926512 m1A Human chr1 + 180814848 180814848 180814848 CGTTTATGCTAGACATTGGTGGAATCAAAGCCATTTCGAGAGAAGGAGACAGTTGAGCAAAGAGA CGTTTATGCTAGACATTGGTGGAATCAAAGCCGTTTCGAGAGAAGGAGACAGTTGAGCAAAGAGA A G XPR1 Ensembl:ENSG00000143324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180814811..180814986 26863196 MeRIP-seq:(Medium) rs529025531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114053,RMVar_hsa_circ_374165,RMVar_hsa_circ_58988,RMVar_hsa_circ_138107,RMVar_hsa_circ_138108,RMVar_hsa_circ_138109,RMVar_hsa_circ_138111,RMVar_hsa_circ_336233,RMVar_hsa_circ_275494,RMVar_hsa_circ_334887,RMVar_hsa_circ_88475,RMVar_hsa_circ_138116,RMVar_hsa_circ_122209,RMVar_hsa_circ_348749,RMVar_hsa_circ_138117,RMVar_hsa_circ_20527 69371 RMVar_ID_69371 Human_SNP_ID_40949030 m1A Human chr1 - 180912189 180912189 180912189 GCAACCAGGGGCATTCCCTGCAGCCGCGGCCCAAACCGACGGAGCTTGCTTTCTCCTTCCACCCA GCAACCAGGGGCATTCCCTGCAGCCGCGGCCCGAACCGACGGAGCTTGCTTTCTCCTTCCACCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:180912145..180912257 32194978 MeRIP-seq:(Medium) rs891272999 Functional Loss SNV dbSNP153 33..33 33 - - - 69372 RMVar_ID_69372 Human_SNP_ID_40960741 m1A Human chr1 + 180954706 180954706 180954706 CATGAGTGTCCCCAGCTTTCAGGCGTGCTGGAAAAACCGCAGGCCGGCTCGAATTTTGGAAACCA CATGAGTGTCCCCAGCTTTCAGGCGTGCTGGAGAAACCGCAGGCCGGCTCGAATTTTGGAAACCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:180954657..180954757 32194978 MeRIP-seq:(Medium) rs908160141 Functional Loss SNV dbSNP153 33..33 33 - - - 69373 RMVar_ID_69373 Human_SNP_ID_40968403 m1A Human chr1 - 180987161 180987161 180987161 GAAAATGCACCTGTGAAGATGGAGAGGTGCACACGTGCATGGAGCAGAGAGGTTCCATGTGTCTG GAAAATGCACCTGTGAAGATGGAGAGGTGCACGCGTGCATGGAGCAGAGAGGTTCCATGTGTCTG T C STX6 Ensembl:ENSG00000135823 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:180987160..180987320 26863196 MeRIP-seq:(Medium) rs906992344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138134,RMVar_hsa_circ_138132,RMVar_hsa_circ_85551,RMVar_hsa_circ_377714,RMVar_hsa_circ_138131,RMVar_hsa_circ_138133,RMVar_hsa_circ_270905,RMVar_hsa_circ_278866,RMVar_hsa_circ_314098,RMVar_hsa_circ_273220,RMVar_hsa_circ_101653,RMVar_hsa_circ_138136,RMVar_hsa_circ_138138,RMVar_hsa_circ_138137,RMVar_hsa_circ_138135 69374 RMVar_ID_69374 Human_SNP_ID_40972732 m1A Human chr1 - 181005463 181005462 181005463 GATTTCTCTCCTTTGCCTCATCTTGATTACAGAGAGGTACAGAAAGCAGTCAACACTGCCCAGGG GATTTCTCTCCTTTGCCTCATCTTGATTACAG_GAGGTACAGAAAGCAGTCAACACTGCCCAGGG CT C STX6 Ensembl:ENSG00000135823 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:181005301..181005517 26863196 MeRIP-seq:(Medium) rs776732013 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_163164 RMVar_hsa_circ_138134,RMVar_hsa_circ_138133,RMVar_hsa_circ_278866,RMVar_hsa_circ_101653,RMVar_hsa_circ_138135,RMVar_hsa_circ_138143,RMVar_hsa_circ_293400,RMVar_hsa_circ_138141,RMVar_hsa_circ_362654,RMVar_hsa_circ_367531,RMVar_hsa_circ_76178,RMVar_hsa_circ_138144,RMVar_hsa_circ_289422,RMVar_hsa_circ_138145 69375 RMVar_ID_69375 Human_SNP_ID_40975178 m1A Human chr1 + 181015062 181015062 181015062 TGCTTGAAACTCTCACTTTCTCTGTCTCTGTGACATTGTGCTGTTCTAGTTTTCTACCAGTTTTC TGCTTGAAACTCTCACTTTCTCTGTCTCTGTGCCATTGTGCTGTTCTAGTTTTCTACCAGTTTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:181015060..181015176 26863196 MeRIP-seq:(Medium) rs1034172316 Functional Loss SNV dbSNP153 33..33 33 - - - 69376 RMVar_ID_69376 Human_SNP_ID_40975179 m1A Human chr1 + 181015062 181015062 181015062 TGCTTGAAACTCTCACTTTCTCTGTCTCTGTGACATTGTGCTGTTCTAGTTTTCTACCAGTTTTC TGCTTGAAACTCTCACTTTCTCTGTCTCTGTGGCATTGTGCTGTTCTAGTTTTCTACCAGTTTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:181015060..181015176 26863196 MeRIP-seq:(Medium) rs1034172316 Functional Loss SNV dbSNP153 33..33 33 - - - 69377 RMVar_ID_69377 Human_SNP_ID_40977208 m1A Human chr1 - 181022704 181022704 181022704 GAGACCGGGAGGCACGGGCGCCCTGTGCGCGGAGGAGGTGAAGGCGGCCGGGGCCGGGACGCCAT GAGACCGGGAGGCACGGGCGCCCTGTGCGCGGGGGAGGTGAAGGCGGCCGGGGCCGGGACGCCAT T C STX6 Ensembl:ENSG00000135823 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:181022603..181022843 26863196 MeRIP-seq:(Medium) rs1165098036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222023,Human_RBP_ID_803485,Human_RBP_ID_859832,Human_RBP_ID_4076242,Human_RBP_ID_5311903,Human_RBP_ID_8940033,Human_RBP_ID_9340418,Human_RBP_ID_9357232,Human_RBP_ID_18928802,Human_RBP_ID_22429895,Human_RBP_ID_26312303,Human_RBP_ID_26767263 Human_Splice_Rec_163153,Human_Splice_Rec_163163 RMVar_hsa_circ_138134,RMVar_hsa_circ_101653 69378 RMVar_ID_69378 Human_SNP_ID_40980502 m1A Human chr1 + 181034065 181034065 181034065 TACCTCTCATCATTGTGTTAATGGTGAAGCACAGCGATTCCCGTGAGTATCCCACGTCCTCTTCT TACCTCTCATCATTGTGTTAATGGTGAAGCACGGCGATTCCCGTGAGTATCCCACGTCCTCTTCT A G MR1 Ensembl:ENSG00000153029 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:181034014..181034089 26863196 MeRIP-seq:(Medium) rs757463971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19039820 Human_Splice_Rec_163183,Human_Splice_Rec_163193,Human_Splice_Rec_163205,Human_Splice_Rec_163211,Human_Splice_Rec_163213,Human_Splice_Rec_163223,Human_Splice_Rec_163231,Human_Splice_Rec_163241,Human_Splice_Rec_163251 69379 RMVar_ID_69379 Human_SNP_ID_40984247 m1A Human chr1 + 181049100 181049100 181049100 ATATTTTCGCCTGGGCGTTTCGGATCCCATCCATGGGGTCCCTGAATTTATTTCGGTTGGGTACG ATATTTTCGCCTGGGCGTTTCGGATCCCATCCGTGGGGTCCCTGAATTTATTTCGGTTGGGTACG A G MR1 Ensembl:ENSG00000153029 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2236410 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_163184,Human_Splice_Rec_163194,Human_Splice_Rec_163206,Human_Splice_Rec_163212,Human_Splice_Rec_163214,Human_Splice_Rec_163224,Human_Splice_Rec_163232,Human_Splice_Rec_163244,Human_Splice_Rec_163252 GWAS_ID_8382 RMVar_hsa_circ_73740,RMVar_hsa_circ_9771 69380 RMVar_ID_69380 Human_SNP_ID_40984264 m1A Human chr1 + 181049136 181049135 181049136 GGTCCCTGAATTTATTTCGGTTGGGTACGTGGACTCGCACCCTATCACCACATATGACAGTGTCA GGTCCCTGAATTTATTTCGGTTGGGTACGTGG_CTCGCACCCTATCACCACATATGACAGTGTCA GA G MR1 Ensembl:ENSG00000153029 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:181049087..181049169 26863196 MeRIP-seq:(Medium) rs1458611101 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22749651 Human_Splice_Rec_163184,Human_Splice_Rec_163194,Human_Splice_Rec_163206,Human_Splice_Rec_163212,Human_Splice_Rec_163214,Human_Splice_Rec_163224,Human_Splice_Rec_163232,Human_Splice_Rec_163244,Human_Splice_Rec_163252 RMVar_hsa_circ_73740,RMVar_hsa_circ_9771 69381 RMVar_ID_69381 Human_SNP_ID_40993883 m1A Human chr1 - 181088811 181088811 181088811 ACGGGAGGCGCAAACAAGTCCGCCCCCTGGGCACACCCTCGATCACCTAAGACTCCGAAGAGAAA ACGGGAGGCGCAAACAAGTCCGCCCCCTGGGCGCACCCTCGATCACCTAAGACTCCGAAGAGAAA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:181088761..181088927 26863196 MeRIP-seq:(Medium) rs895250030 Functional Loss SNV dbSNP153 33..33 33 - - - 69382 RMVar_ID_69382 Human_SNP_ID_40993905 m1A Human chr1 + 181088861 181088861 181088861 GTTTGCGCCTCCCGTTCCCTCCCAATTTCCAAACGTGTCACCCCGGCGCCGACGGCCCTGTGCAG GTTTGCGCCTCCCGTTCCCTCCCAATTTCCAAGCGTGTCACCCCGGCGCCGACGGCCCTGTGCAG A G IER5 Ensembl:ENSG00000162783 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:181088811..181089111 32194978 MeRIP-seq:(Medium) rs374640718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973324,Human_RBP_ID_5413293,Human_RBP_ID_5433278,Human_RBP_ID_5456732,Human_RBP_ID_5484979,Human_RBP_ID_8044910,Human_RBP_ID_9319274,Human_RBP_ID_17732974,Human_RBP_ID_22024036,Human_RBP_ID_27172509 69383 RMVar_ID_69383 Human_SNP_ID_40994053 m1A Human chr1 - 181089149 181089149 181089149 GGCACGAGCGGCGGGCGGGGGCGGCTCTCCCCAGCCGGCGGGTGGCCCGGCCGCCGGCTCCCCGG GGCACGAGCGGCGGGCGGGGGCGGCTCTCCCCCGCCGGCGGGTGGCCCGGCCGCCGGCTCCCCGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:181089101..181089400 26863196 MeRIP-seq:(Medium) rs966911917 Functional Loss SNV dbSNP153 33..33 33 - - - 69384 RMVar_ID_69384 Human_SNP_ID_40994134 m1A Human chr1 - 181089267 181089267 181089267 CTCCGCCCTGAAAAACGTCCCCGACTCCAGTCACCGTGGCCACCGGCACCTCGTCCCCTACCCGC CTCCGCCCTGAAAAACGTCCCCGACTCCAGTCGCCGTGGCCACCGGCACCTCGTCCCCTACCCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:181089097..181089376 26863196 MeRIP-seq:(Medium) rs753114362 Functional Loss SNV dbSNP153 33..33 33 - - - 69385 RMVar_ID_69385 Human_SNP_ID_40994145 m1A Human chr1 + 181089282 181089282 181089282 GGTGCCGGTGGCCACGGTGACTGGAGTCGGGGACGTTTTTCAGGGCGGAGAGGCGGACGCGACGG GGTGCCGGTGGCCACGGTGACTGGAGTCGGGGGCGTTTTTCAGGGCGGAGAGGCGGACGCGACGG A G IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:181088701..181089496 26863196 MeRIP-seq:(Medium) rs867918361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554,Human_RBP_ID_17668325,Human_RBP_ID_18557691,Human_RBP_ID_22026099 69386 RMVar_ID_69386 Human_SNP_ID_40994152 m1A Human chr1 + 181089291 181089291 181089291 GGCCACGGTGACTGGAGTCGGGGACGTTTTTCAGGGCGGAGAGGCGGACGCGACGGAAGCTGCCT GGCCACGGTGACTGGAGTCGGGGACGTTTTTCGGGGCGGAGAGGCGGACGCGACGGAAGCTGCCT A G IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:181088701..181089981 26863196 MeRIP-seq:(Medium) rs748744688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554,Human_RBP_ID_4011517,Human_RBP_ID_17668325,Human_RBP_ID_22024039,Human_RBP_ID_22132112,Human_RBP_ID_26848224 69387 RMVar_ID_69387 Human_SNP_ID_40994171 m1A Human chr1 - 181089323 181089323 181089323 CGCCGCCTGGCGCGGCCCCTCCACGCGGCTCCAGGCAGCTTCCGTCGCGTCCGCCTCTCCGCCCT CGCCGCCTGGCGCGGCCCCTCCACGCGGCTCCGGGCAGCTTCCGTCGCGTCCGCCTCTCCGCCCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr1:181089026..181089400;chr1:181089230..181089401 26863196 MeRIP-seq:(Medium) rs775918481 Functional Loss SNV dbSNP153 33..33 33 - - - 69388 RMVar_ID_69388 Human_SNP_ID_40994183 m1A Human chr1 + 181089359 181089359 181089359 GCCGCGTGGAGGGGCCGCGCCAGGCGGCGGCCAGAGAAGCCGAGGGTACCGCCGGAGGCTGGGGC GCCGCGTGGAGGGGCCGCGCCAGGCGGCGGCCGGAGAAGCCGAGGGTACCGCCGGAGGCTGGGGC A G IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:181089309..181089460 32194978 MeRIP-seq:(Medium) rs1221707914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22024040,Human_RBP_ID_22427719 69389 RMVar_ID_69389 Human_SNP_ID_40994398 m1A Human chr1 + 181089672 181089672 181089672 AGAGCAGCCGCCGAGTGGAGGAGAGGACGACGACGCGGAGGAGATGGAGACCGGGAACGTGGCTA AGAGCAGCCGCCGAGTGGAGGAGAGGACGACGCCGCGGAGGAGATGGAGACCGGGAACGTGGCTA A C IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:181089160..181089995 26863196 MeRIP-seq:(Medium) rs918696136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4011534,Human_RBP_ID_5724844,Human_RBP_ID_22870999 69390 RMVar_ID_69390 Human_SNP_ID_40994480 m1A Human chr1 - 181089827 181089827 181089827 GGGGTTCATGTCTCTCAGCACCGGCTTATCGCAGCAGATCTGCCCGGGCTCGGCGGCTTCCGGAC GGGGTTCATGTCTCTCAGCACCGGCTTATCGCGGCAGATCTGCCCGGGCTCGGCGGCTTCCGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:181088701..181089964 26863196 MeRIP-seq:(Medium) rs777823916 Functional Loss SNV dbSNP153 33..33 33 - - - 69391 RMVar_ID_69391 Human_SNP_ID_40994522 m1A Human chr1 + 181089908 181089908 181089908 TGGCCTTCTGAGCCCTTGGCCCCCCTGCGGGGAGGAGGTGGAGCAGCGGGCGTCCCCGAAGTGAG TGGCCTTCTGAGCCCTTGGCCCCCCTGCGGGGGGGAGGTGGAGCAGCGGGCGTCCCCGAAGTGAG A G IER5 Ensembl:ENSG00000162783 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:181089808..181090108 26863410 MeRIP-seq:(Medium) rs974102533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9270501,Human_RBP_ID_22024043,Human_RBP_ID_22427722,Human_RBP_ID_23349880,Human_RBP_ID_26312307,Human_RBP_ID_26767606 69392 RMVar_ID_69392 Human_SNP_ID_41214425 m1A Human chr1 - 182029395 182029395 182029395 GACCGGAAGATGGAAGGAATTCGCTAGGCCAGAGGCGGGAGGGTGCCCAGGGGAGGGGACAGAGT GACCGGAAGATGGAAGGAATTCGCTAGGCCAGGGGCGGGAGGGTGCCCAGGGGAGGGGACAGAGT T C lnc-ZNF648-6 RNACentral:URS0000D5BAB2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:182029346..182029586 26863196 MeRIP-seq:(Medium) rs1238255987 Functional Loss SNV dbSNP153 33..33 33 - - - 69393 RMVar_ID_69393 Human_SNP_ID_41296903 m1A Human chr1 - 182383486 182383486 182383486 GGAGAAGGTGGGCACTGGATTAGTTAACAGACAACACGTTACTAGCAGTCACTTGATCTCCGTGG GGAGAAGGTGGGCACTGGATTAGTTAACAGACTACACGTTACTAGCAGTCACTTGATCTCCGTGG T A GLUL Ensembl:ENSG00000135821 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334970,Human_RBP_ID_4085805,Human_RBP_ID_5725084,Human_RBP_ID_10687413,Human_RBP_ID_17338575,Human_RBP_ID_18220898,Human_RBP_ID_23349950,Human_RBP_ID_26372875 Human_miRNA_ID_2036212,Human_miRNA_ID_2346911 Clinvar_Rec_283,Clinvar_Rec_2456 GWAS_ID_8383,GWAS_ID_8384 RMVar_hsa_circ_123570,RMVar_hsa_circ_138181 69394 RMVar_ID_69394 Human_SNP_ID_41296904 m1A Human chr1 - 182383486 182383486 182383486 GGAGAAGGTGGGCACTGGATTAGTTAACAGACAACACGTTACTAGCAGTCACTTGATCTCCGTGG GGAGAAGGTGGGCACTGGATTAGTTAACAGACGACACGTTACTAGCAGTCACTTGATCTCCGTGG T C GLUL Ensembl:ENSG00000135821 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334970,Human_RBP_ID_4085805,Human_RBP_ID_5725084,Human_RBP_ID_10687413,Human_RBP_ID_17338575,Human_RBP_ID_18220898,Human_RBP_ID_23349950,Human_RBP_ID_26372875 Human_miRNA_ID_2036212,Human_miRNA_ID_2346911 Clinvar_Rec_283,Clinvar_Rec_2456 GWAS_ID_8383,GWAS_ID_8384 RMVar_hsa_circ_123570,RMVar_hsa_circ_138181 69395 RMVar_ID_69395 Human_SNP_ID_41297218 m1A Human chr1 - 182384471 182384471 182384471 CCCTCTGCCAACTGCGACCCCTTTTCGGTGACAGAAGCCCTCATCCGCACGTGTCTTCTCAATGA CCCTCTGCCAACTGCGACCCCTTTTCGGTGACGGAAGCCCTCATCCGCACGTGTCTTCTCAATGA T C GLUL Ensembl:ENSG00000135821 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:182384326..182384579 26863196 MeRIP-seq:(Medium) rs201149359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335009,Human_RBP_ID_4011692,Human_RBP_ID_8959710,Human_RBP_ID_22024046,Human_RBP_ID_22427723,Human_RBP_ID_26848287 RMVar_hsa_circ_123570,RMVar_hsa_circ_138181 69396 RMVar_ID_69396 Human_SNP_ID_41297492 m1A Human chr1 + 182385319 182385319 182385319 AGATTGCTAAGTCTCCTCCCAAGTTTTCTGCCACAGGAGATTAAAGATGGCCCCAGCAGAAGGTA AGATTGCTAAGTCTCCTCCCAAGTTTTCTGCCCCAGGAGATTAAAGATGGCCCCAGCAGAAGGTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182385316..182385584 26863196 MeRIP-seq:(Medium) rs774201990 Functional Loss SNV dbSNP153 33..33 33 - - - 69397 RMVar_ID_69397 Human_SNP_ID_41297493 m1A Human chr1 + 182385319 182385319 182385319 AGATTGCTAAGTCTCCTCCCAAGTTTTCTGCCACAGGAGATTAAAGATGGCCCCAGCAGAAGGTA AGATTGCTAAGTCTCCTCCCAAGTTTTCTGCCGCAGGAGATTAAAGATGGCCCCAGCAGAAGGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182385316..182385584 26863196 MeRIP-seq:(Medium) rs774201990 Functional Loss SNV dbSNP153 33..33 33 - - - 69398 RMVar_ID_69398 Human_SNP_ID_41297806 m1A Human chr1 - 182386253 182386253 182386253 GGCCTTCCAACGGCTTCCCAGGGCCCCAGGGTAAGTCTCCTTGGGTTAGAGGTGAAATTCCCAGA GGCCTTCCAACGGCTTCCCAGGGCCCCAGGGTGAGTCTCCTTGGGTTAGAGGTGAAATTCCCAGA T C GLUL Ensembl:ENSG00000135821 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:182386251..182386425 32194978 MeRIP-seq:(Medium) rs773158980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858596,Human_RBP_ID_8959720,Human_RBP_ID_19035755,Human_RBP_ID_22428744,Human_RBP_ID_26315091 RMVar_hsa_circ_20544,RMVar_hsa_circ_123570,RMVar_hsa_circ_127428,RMVar_hsa_circ_138181,RMVar_hsa_circ_345628,RMVar_hsa_circ_138182,RMVar_hsa_circ_357572 69399 RMVar_ID_69399 Human_SNP_ID_41298117 m1A Human chr1 + 182387204 182387204 182387204 AGCTTGTTAGGGTCCTTACGGAAGGGGTCCCGAAACATGGCAGCAGGCACGAGATACATGTCACT AGCTTGTTAGGGTCCTTACGGAAGGGGTCCCGGAACATGGCAGCAGGCACGAGATACATGTCACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182387097..182387310 26863196 MeRIP-seq:(Medium) rs755338601 Functional Loss SNV dbSNP153 33..33 33 - - - 69400 RMVar_ID_69400 Human_SNP_ID_41298528 m1A Human chr1 - 182388747 182388747 182388747 AACAATGTTATTCTTTTTTTCTTCTCCAGAACACCTTCCACCATGACCACCTCAGCAAGTTCCCA AACAATGTTATTCTTTTTTTCTTCTCCAGAACTCCTTCCACCATGACCACCTCAGCAAGTTCCCA T A GLUL Ensembl:ENSG00000135821 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:182388739..182388826 26863410 MeRIP-seq:(Medium) rs1253215879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746563 Human_Splice_Rec_164102,Human_Splice_Rec_164116,Human_Splice_Rec_164128,Human_Splice_Rec_164142,Human_Splice_Rec_164156,Human_Splice_Rec_164168,Human_Splice_Rec_164178,Human_Splice_Rec_164188,Human_Splice_Rec_164202,Human_Splice_Rec_164208 RMVar_hsa_circ_39192,RMVar_hsa_circ_20544,RMVar_hsa_circ_345628 69401 RMVar_ID_69401 Human_SNP_ID_41299428 m1A Human chr1 + 182391729 182391729 182391729 GGCGGGTAAAGCTAGGCCGCGAGAGCGAGGTTAGGAGAGGAGAGGAGGCCGCAGTACTGCTCACA GGCGGGTAAAGCTAGGCCGCGAGAGCGAGGTTTGGAGAGGAGAGGAGGCCGCAGTACTGCTCACA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:182391656..182391757 32194978 MeRIP-seq:(Medium) rs938926567 Functional Loss SNV dbSNP153 33..33 33 - - - 69402 RMVar_ID_69402 Human_SNP_ID_41299431 m1A Human chr1 + 182391732 182391732 182391732 GGGTAAAGCTAGGCCGCGAGAGCGAGGTTAGGAGAGGAGAGGAGGCCGCAGTACTGCTCACACGC GGGTAAAGCTAGGCCGCGAGAGCGAGGTTAGGCGAGGAGAGGAGGCCGCAGTACTGCTCACACGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182391627..182391800 26863196 MeRIP-seq:(Medium) rs577589374 Functional Loss SNV dbSNP153 33..33 33 - - - 69403 RMVar_ID_69403 Human_SNP_ID_41299433 m1A Human chr1 + 182391737 182391737 182391737 AAGCTAGGCCGCGAGAGCGAGGTTAGGAGAGGAGAGGAGGCCGCAGTACTGCTCACACGCTCCGC AAGCTAGGCCGCGAGAGCGAGGTTAGGAGAGGGGAGGAGGCCGCAGTACTGCTCACACGCTCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:182391536..182391740 26863196 MeRIP-seq:(Medium) rs1172579206 Functional Loss SNV dbSNP153 33..33 33 - - - 69404 RMVar_ID_69404 Human_SNP_ID_41299446 m1A Human chr1 - 182391751 182391751 182391751 AGAGTGGGAGAAGAGCGGAGCGTGTGAGCAGTACTGCGGCCTCCTCTCCTCTCCTAACCTCGCTC AGAGTGGGAGAAGAGCGGAGCGTGTGAGCAGTCCTGCGGCCTCCTCTCCTCTCCTAACCTCGCTC T G GLUL Ensembl:ENSG00000135821 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:182391481..182391750 26863196 MeRIP-seq:(Medium) rs1303331043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335021,Human_RBP_ID_4011762,Human_RBP_ID_5158697,Human_RBP_ID_5413299,Human_RBP_ID_5456744,Human_RBP_ID_5484991,Human_RBP_ID_5519962,Human_RBP_ID_5725186,Human_RBP_ID_8755270,Human_RBP_ID_22429912,Human_RBP_ID_23123155 Human_Splice_Rec_164101,Human_Splice_Rec_164139,Human_Splice_Rec_164167,Human_Splice_Rec_164187,Human_Splice_Rec_164199,Human_Splice_Rec_164207 69405 RMVar_ID_69405 Human_SNP_ID_41394718 m1A Human chr1 - 182789380 182789380 182789380 TCCGCTGCGTCTTAATTTTCCTTCTCTTGCGCAGGGCTCTGCAATCCCCACTATCTCGTGGTTCT TCCGCTGCGTCTTAATTTTCCTTCTCTTGCGCGGGGCTCTGCAATCCCCACTATCTCGTGGTTCT T C HSALNG0008944 RNACentral:URS0000E9D4EF lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:182789333..182789434 26863196 MeRIP-seq:(Medium) rs995340092 Functional Loss SNV dbSNP153 33..33 33 - - - 69406 RMVar_ID_69406 Human_SNP_ID_41394754 m1A Human chr1 + 182789511 182789511 182789511 GCGTGGCGCGGGTGAGCCGCGTGCTCTCGGGCACCCGGCCGCCAGTTCGGATGCTTCCGATCCTC GCGTGGCGCGGGTGAGCCGCGTGCTCTCGGGCCCCCGGCCGCCAGTTCGGATGCTTCCGATCCTC A C NPL Ensembl:ENSG00000135838 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182789462..182789565 26863196 MeRIP-seq:(Medium) rs902084396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76384,RMVar_hsa_circ_138186 69407 RMVar_ID_69407 Human_SNP_ID_41394897 m1A Human chr1 - 182789807 182789807 182789807 TGTCCTAGCCCGTGCCGTCGCGGGCCGCGCTCACCCAGGCCTCCGCTCTTGTCCGTGCAGCCGCT TGTCCTAGCCCGTGCCGTCGCGGGCCGCGCTCGCCCAGGCCTCCGCTCTTGTCCGTGCAGCCGCT T C HSALNG0008944 RNACentral:URS0000E9D4EF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:182789789..182789957;chr1:182789502..182790003;chr1:182789572..182789991;chr1:182789640..182790004 26863196 MeRIP-seq:(Medium) rs1441532003 Functional Loss SNV dbSNP153 33..33 33 - - - 69408 RMVar_ID_69408 Human_SNP_ID_41406073 m1A Human chr1 - 182839727 182839725 182839727 CGGTGCCCCGGCGTACGCAGGCCAGAGGAGGAAGCGCGCTTTGCCTGCTAGAGGCAGCAGCGGGA CGGTGCCCCGGCGTACGCAGGCCAGAGGAGGA__CGCGCTTTGCCTGCTAGAGGCAGCAGCGGGA GCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:182839722..182840263 26863196 MeRIP-seq:(Medium) rs573721488 Functional Loss DEL dbSNP153 33..34 33 - - - 69409 RMVar_ID_69409 Human_SNP_ID_41406082 m1A Human chr1 - 182839736 182839736 182839736 CAGCCGCCGCGGTGCCCCGGCGTACGCAGGCCAGAGGAGGAAGCGCGCTTTGCCTGCTAGAGGCA CAGCCGCCGCGGTGCCCCGGCGTACGCAGGCCGGAGGAGGAAGCGCGCTTTGCCTGCTAGAGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182839735..182839911 26863196 MeRIP-seq:(Medium) rs372286736 Functional Loss SNV dbSNP153 33..33 33 - - - 69410 RMVar_ID_69410 Human_SNP_ID_41406992 m1A Human chr1 + 182842496 182842496 182842496 AGATTCAGTAATCTAGATAATTGGTTCCTCCCAGTTTTTGCTATTATAAATGCTGTTTTTAACTG AGATTCAGTAATCTAGATAATTGGTTCCTCCCGGTTTTTGCTATTATAAATGCTGTTTTTAACTG A G DHX9 Ensembl:ENSG00000135829 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:182842493..182842643 26863196 MeRIP-seq:(Medium) rs1389836854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24614465 69411 RMVar_ID_69411 Human_SNP_ID_41416527 m1A Human chr1 + 182878084 182878084 182878084 AATATGACCAACTATGCTACCGTATGGGCATCAAAAACAAACCTTGAGCAACGGAAAGGGCGAGC AATATGACCAACTATGCTACCGTATGGGCATCCAAAACAAACCTTGAGCAACGGAAAGGGCGAGC A C DHX9 Ensembl:ENSG00000135829 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1237601756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20248,Human_RBP_ID_973401,Human_RBP_ID_1416951,Human_RBP_ID_1731204,Human_RBP_ID_8739358,Human_RBP_ID_9267009,Human_RBP_ID_17448053,Human_RBP_ID_18429071,Human_RBP_ID_18557841,Human_RBP_ID_22781485,Human_RBP_ID_26799265,Human_RBP_ID_27582935 Human_Splice_Rec_164860,Human_Splice_Rec_164861,Human_Splice_Rec_164898,Human_Splice_Rec_164899,Human_Splice_Rec_164907 RMVar_hsa_circ_118315,RMVar_hsa_circ_138188,RMVar_hsa_circ_106250,RMVar_hsa_circ_369682,RMVar_hsa_circ_40506,RMVar_hsa_circ_119190,RMVar_hsa_circ_138196,RMVar_hsa_circ_138197,RMVar_hsa_circ_138201,RMVar_hsa_circ_94850,RMVar_hsa_circ_138200,RMVar_hsa_circ_8279,RMVar_hsa_circ_375418,RMVar_hsa_circ_138206,RMVar_hsa_circ_41823,RMVar_hsa_circ_138207,RMVar_hsa_circ_110746,RMVar_hsa_circ_78873,RMVar_hsa_circ_138209,RMVar_hsa_circ_138210,RMVar_hsa_circ_106192,RMVar_hsa_circ_138212,RMVar_hsa_circ_138211,RMVar_hsa_circ_370305,RMVar_hsa_circ_297181,RMVar_hsa_circ_314269,RMVar_hsa_circ_98060,RMVar_hsa_circ_138214,RMVar_hsa_circ_37128,RMVar_hsa_circ_54420,RMVar_hsa_circ_308336,RMVar_hsa_circ_138213,RMVar_hsa_circ_350031,RMVar_hsa_circ_302381,RMVar_hsa_circ_115778,RMVar_hsa_circ_138215,RMVar_hsa_circ_72758,RMVar_hsa_circ_107406,RMVar_hsa_circ_123203,RMVar_hsa_circ_138216,RMVar_hsa_circ_138219,RMVar_hsa_circ_83799,RMVar_hsa_circ_138218,RMVar_hsa_circ_138220 69412 RMVar_ID_69412 Human_SNP_ID_41416528 m1A Human chr1 + 182878084 182878084 182878084 AATATGACCAACTATGCTACCGTATGGGCATCAAAAACAAACCTTGAGCAACGGAAAGGGCGAGC AATATGACCAACTATGCTACCGTATGGGCATCGAAAACAAACCTTGAGCAACGGAAAGGGCGAGC A G DHX9 Ensembl:ENSG00000135829 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1237601756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20248,Human_RBP_ID_973401,Human_RBP_ID_1416951,Human_RBP_ID_1731204,Human_RBP_ID_8739358,Human_RBP_ID_9267009,Human_RBP_ID_17448053,Human_RBP_ID_18429071,Human_RBP_ID_18557841,Human_RBP_ID_22781485,Human_RBP_ID_26799265,Human_RBP_ID_27582935 Human_Splice_Rec_164860,Human_Splice_Rec_164861,Human_Splice_Rec_164898,Human_Splice_Rec_164899,Human_Splice_Rec_164907 RMVar_hsa_circ_118315,RMVar_hsa_circ_138188,RMVar_hsa_circ_106250,RMVar_hsa_circ_369682,RMVar_hsa_circ_40506,RMVar_hsa_circ_119190,RMVar_hsa_circ_138196,RMVar_hsa_circ_138197,RMVar_hsa_circ_138201,RMVar_hsa_circ_94850,RMVar_hsa_circ_138200,RMVar_hsa_circ_8279,RMVar_hsa_circ_375418,RMVar_hsa_circ_138206,RMVar_hsa_circ_41823,RMVar_hsa_circ_138207,RMVar_hsa_circ_110746,RMVar_hsa_circ_78873,RMVar_hsa_circ_138209,RMVar_hsa_circ_138210,RMVar_hsa_circ_106192,RMVar_hsa_circ_138212,RMVar_hsa_circ_138211,RMVar_hsa_circ_370305,RMVar_hsa_circ_297181,RMVar_hsa_circ_314269,RMVar_hsa_circ_98060,RMVar_hsa_circ_138214,RMVar_hsa_circ_37128,RMVar_hsa_circ_54420,RMVar_hsa_circ_308336,RMVar_hsa_circ_138213,RMVar_hsa_circ_350031,RMVar_hsa_circ_302381,RMVar_hsa_circ_115778,RMVar_hsa_circ_138215,RMVar_hsa_circ_72758,RMVar_hsa_circ_107406,RMVar_hsa_circ_123203,RMVar_hsa_circ_138216,RMVar_hsa_circ_138219,RMVar_hsa_circ_83799,RMVar_hsa_circ_138218,RMVar_hsa_circ_138220 69413 RMVar_ID_69413 Human_SNP_ID_41452105 m1A Human chr1 - 183023471 183023471 183023471 GCCGCCTCCGCGCTTCCCTCACCTACCCCGGGAGCAGCCTGCACTCCGCGCCGACCCCCGACTTC GCCGCCTCCGCGCTTCCCTCACCTACCCCGGGGGCAGCCTGCACTCCGCGCCGACCCCCGACTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:183023424..183024075 26863196 MeRIP-seq:(Medium) rs1412181055 Functional Loss SNV dbSNP153 33..33 33 - - - 69414 RMVar_ID_69414 Human_SNP_ID_41470712 m1A Human chr1 + 183103525 183103525 183103525 GGACAGGAGGGGACGAGCAGCAGGCCTTGTGTACTGATGAATTCAGTGACATTTCTCCCCTCACT GGACAGGAGGGGACGAGCAGCAGGCCTTGTGTGCTGATGAATTCAGTGACATTTCTCCCCTCACT A G LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:183103476..183103550 32194978 MeRIP-seq:(Medium) rs1182701637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23350286 RMVar_hsa_circ_123882,RMVar_hsa_circ_138227,RMVar_hsa_circ_108137,RMVar_hsa_circ_138226 69415 RMVar_ID_69415 Human_SNP_ID_41474174 m1A Human chr1 + 183117428 183117428 183117428 CGCCGTGATCTCAGACAGCTACTTTCCTCGGTACTTCATTGCTCCTGGTAAGTAAGGCTAGAAAG CGCCGTGATCTCAGACAGCTACTTTCCTCGGTGCTTCATTGCTCCTGGTAAGTAAGGCTAGAAAG A G LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:183117377..183118077 32194978 MeRIP-seq:(Medium) rs538012337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8739396,Human_RBP_ID_17764970,Human_RBP_ID_18557911,Human_RBP_ID_19039842 Human_Splice_Rec_165017 RMVar_hsa_circ_6150,RMVar_hsa_circ_92099,RMVar_hsa_circ_9859,RMVar_hsa_circ_138227,RMVar_hsa_circ_108137,RMVar_hsa_circ_347367,RMVar_hsa_circ_272197,RMVar_hsa_circ_95728,RMVar_hsa_circ_138229,RMVar_hsa_circ_138231,RMVar_hsa_circ_86229,RMVar_hsa_circ_138230,RMVar_hsa_circ_138233,RMVar_hsa_circ_80397,RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_138235,RMVar_hsa_circ_302686,RMVar_hsa_circ_47199,RMVar_hsa_circ_354107 69416 RMVar_ID_69416 Human_SNP_ID_41474175 m1A Human chr1 + 183117428 183117428 183117428 CGCCGTGATCTCAGACAGCTACTTTCCTCGGTACTTCATTGCTCCTGGTAAGTAAGGCTAGAAAG CGCCGTGATCTCAGACAGCTACTTTCCTCGGTTCTTCATTGCTCCTGGTAAGTAAGGCTAGAAAG A T LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:183117377..183118077 32194978 MeRIP-seq:(Medium) rs538012337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8739396,Human_RBP_ID_17764970,Human_RBP_ID_18557911,Human_RBP_ID_19039842 Human_Splice_Rec_165017 RMVar_hsa_circ_6150,RMVar_hsa_circ_92099,RMVar_hsa_circ_9859,RMVar_hsa_circ_138227,RMVar_hsa_circ_108137,RMVar_hsa_circ_347367,RMVar_hsa_circ_272197,RMVar_hsa_circ_95728,RMVar_hsa_circ_138229,RMVar_hsa_circ_138231,RMVar_hsa_circ_86229,RMVar_hsa_circ_138230,RMVar_hsa_circ_138233,RMVar_hsa_circ_80397,RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_138235,RMVar_hsa_circ_302686,RMVar_hsa_circ_47199,RMVar_hsa_circ_354107 69417 RMVar_ID_69417 Human_SNP_ID_41476460 m1A Human chr1 - 183126201 183126201 183126201 TGGTTGACCTCACAGCGCTCACAGTGCTGACCAGTGATGCCGGGCTGGCACTCACACTGGCCGGT TGGTTGACCTCACAGCGCTCACAGTGCTGACCCGTGATGCCGGGCTGGCACTCACACTGGCCGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:183126101..183126200 32194978 MeRIP-seq:(Medium) rs1422015399 Functional Loss SNV dbSNP153 33..33 33 - - - 69418 RMVar_ID_69418 Human_SNP_ID_41478603 m1A Human chr1 + 183133457 183133457 183133457 ATCTCACAGGATCTGGAAAAACAAGCTGCCCGAGTACATGAGGAGGCCAAAAGGGCCGGTGACAA ATCTCACAGGATCTGGAAAAACAAGCTGCCCGTGTACATGAGGAGGCCAAAAGGGCCGGTGACAA A T LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:183133378..183133539 26863196 MeRIP-seq:(Medium) rs1458160772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20297,Human_RBP_ID_335115,Human_RBP_ID_858652,Human_RBP_ID_9357271,Human_RBP_ID_17733180,Human_RBP_ID_26848476 Human_Splice_Rec_165042,Human_Splice_Rec_165043,Human_Splice_Rec_165082 RMVar_hsa_circ_9859,RMVar_hsa_circ_95728,RMVar_hsa_circ_138229,RMVar_hsa_circ_138233,RMVar_hsa_circ_80397,RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_354107,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_121166,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_138238,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_126459,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138242,RMVar_hsa_circ_368776,RMVar_hsa_circ_138243,RMVar_hsa_circ_343159,RMVar_hsa_circ_138244,RMVar_hsa_circ_118791,RMVar_hsa_circ_127459,RMVar_hsa_circ_301166,RMVar_hsa_circ_138245 69419 RMVar_ID_69419 Human_SNP_ID_41479049 m1A Human chr1 - 183135139 183135139 183135139 CTCAGCCTTTTCTACCTTTCAGGTTGTTGAGAATGTCATTAGCTTCTTGTAAGGTATCCCGTCCC CTCAGCCTTTTCTACCTTTCAGGTTGTTGAGACTGTCATTAGCTTCTTGTAAGGTATCCCGTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:183135088..183135189 26863196 MeRIP-seq:(Medium) rs762909421 Functional Loss SNV dbSNP153 33..33 33 - - - 69420 RMVar_ID_69420 Human_SNP_ID_41479053 m1A Human chr1 + 183135155 183135155 183135155 CAAGAAGCTAATGACATTCTCAACAACCTGAAAGGTAGAAAAGGCTGAGATAACAGGGGCAAATG CAAGAAGCTAATGACATTCTCAACAACCTGAAGGGTAGAAAAGGCTGAGATAACAGGGGCAAATG A G LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:183135120..183136450 32194978 MeRIP-seq:(Medium) rs199831296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9357278 Human_Splice_Rec_165047,Human_Splice_Rec_165085 RMVar_hsa_circ_138233,RMVar_hsa_circ_80397,RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_354107,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_121166,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_138238,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_126459,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138242,RMVar_hsa_circ_368776,RMVar_hsa_circ_138243,RMVar_hsa_circ_138244,RMVar_hsa_circ_127459,RMVar_hsa_circ_301166,RMVar_hsa_circ_111287,RMVar_hsa_circ_138246 69421 RMVar_ID_69421 Human_SNP_ID_41479424 m1A Human chr1 + 183136476 183136476 183136476 TCCTGCCATCAACCAGACCATCACTGAAGCCAATGAAAAGACCAGAGAAGCCCAGCAGGCCCTGG TCCTGCCATCAACCAGACCATCACTGAAGCCAGTGAAAAGACCAGAGAAGCCCAGCAGGCCCTGG A G LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:183136426..183136475 26863196 MeRIP-seq:(Medium) rs771235090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858655,Human_RBP_ID_8228409,Human_RBP_ID_9357281,Human_RBP_ID_26309864 Human_Splice_Rec_165048,Human_Splice_Rec_165086 Human_miRNA_ID_3115742 RMVar_hsa_circ_138233,RMVar_hsa_circ_80397,RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_354107,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_121166,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_138238,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_126459,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138242,RMVar_hsa_circ_138243,RMVar_hsa_circ_138244,RMVar_hsa_circ_127459,RMVar_hsa_circ_111287,RMVar_hsa_circ_138246 69422 RMVar_ID_69422 Human_SNP_ID_41480956 m1A Human chr1 + 183142743 183142743 183142743 AGGACATTCGCAATCTGGAGGACATCAGGAAGACCTTACCATCTGGCTGCTTCAACACCCCGTCC AGGACATTCGCAATCTGGAGGACATCAGGAAGTCCTTACCATCTGGCTGCTTCAACACCCCGTCC A T LAMC1 Ensembl:ENSG00000135862 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1166097824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335117,Human_RBP_ID_1731310,Human_RBP_ID_5726004,Human_RBP_ID_9357289,Human_RBP_ID_17764981 RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138243 69423 RMVar_ID_69423 Human_SNP_ID_41480980 m1A Human chr1 + 183142825 183142824 183142826 TCTTTAGGGCTGGAAGGCAGCATCCCTCTGACAGGGGGGCAGTTGTGAGGCCACAGAGTGCCTTG TCTTTAGGGCTGGAAGGCAGCATCCCTCTGAC__GGGGGCAGTTGTGAGGCCACAGAGTGCCTTG CAG C LAMC1 Ensembl:ENSG00000135862 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:183142776..183143000 32194978 MeRIP-seq:(Medium) rs199548614 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_189814,Human_RBP_ID_742931,Human_RBP_ID_802956,Human_RBP_ID_858665,Human_RBP_ID_1731311,Human_RBP_ID_5726005,Human_RBP_ID_9357291,Human_RBP_ID_17223571,Human_RBP_ID_17456352 Human_miRNA_ID_958849,Human_miRNA_ID_975021,Human_miRNA_ID_2150461,Human_miRNA_ID_2418957,Human_miRNA_ID_2443378 RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138243 69424 RMVar_ID_69424 Human_SNP_ID_41480985 m1A Human chr1 + 183142825 183142825 183142825 TCTTTAGGGCTGGAAGGCAGCATCCCTCTGACAGGGGGGCAGTTGTGAGGCCACAGAGTGCCTTG TCTTTAGGGCTGGAAGGCAGCATCCCTCTGACGGGGGGGCAGTTGTGAGGCCACAGAGTGCCTTG A G LAMC1 Ensembl:ENSG00000135862 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:183142776..183143000 32194978 MeRIP-seq:(Medium) rs979252161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189814,Human_RBP_ID_742931,Human_RBP_ID_802956,Human_RBP_ID_858665,Human_RBP_ID_1731311,Human_RBP_ID_5726005,Human_RBP_ID_9357291,Human_RBP_ID_17223571,Human_RBP_ID_17456352 Human_miRNA_ID_958849,Human_miRNA_ID_975021,Human_miRNA_ID_2150461,Human_miRNA_ID_2418957,Human_miRNA_ID_2443378 RMVar_hsa_circ_116173,RMVar_hsa_circ_138234,RMVar_hsa_circ_83875,RMVar_hsa_circ_93171,RMVar_hsa_circ_138237,RMVar_hsa_circ_138239,RMVar_hsa_circ_110311,RMVar_hsa_circ_77036,RMVar_hsa_circ_138240,RMVar_hsa_circ_138241,RMVar_hsa_circ_95631,RMVar_hsa_circ_138243 69425 RMVar_ID_69425 Human_SNP_ID_41545544 m1A Human chr1 + 183412144 183412144 183412144 GATGACTTTGACTTTGATTGACAGAGATACGGAGCTCTGGAGGATTTGGAGCAAAGGAGCAACAT GATGACTTTGACTTTGATTGACAGAGATACGGCGCTCTGGAGGATTTGGAGCAAAGGAGCAACAT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:183412023..183412150 26863196 MeRIP-seq:(Medium) rs1048548049 Functional Loss SNV dbSNP153 33..33 33 - - - 69426 RMVar_ID_69426 Human_SNP_ID_41559780 m1A Human chr1 - 183472546 183472546 183472546 GTCTCTCAGGCTCCTCGGAGCGGCCCCGCGGCACCGCGGGTGCTGGCGGCCGCCGCCATCTTCCT GTCTCTCAGGCTCCTCGGAGCGGCCCCGCGGCCCCGCGGGTGCTGGCGGCCGCCGCCATCTTCCT T G SMG7-AS1,SMG7-AS1:2 RNACentral:URS00008B8119,RNACentral:URS00009C5D7F lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr1:183472495..183472660;chr1:183472501..183472643;chr1:183472501..183472753 26863196 MeRIP-seq:(Medium) rs1417750028 Functional Loss SNV dbSNP153 33..33 33 - - - 69427 RMVar_ID_69427 Human_SNP_ID_41559813 m1A Human chr1 + 183472633 183472633 183472633 CGCGGCGGCGGCGGCGGAGGATGAGCCTGCAGAGCGCGCAGTACCTCCGGTGAGTGCCGAGGCCG CGCGGCGGCGGCGGCGGAGGATGAGCCTGCAGTGCGCGCAGTACCTCCGGTGAGTGCCGAGGCCG A T SMG7 Ensembl:ENSG00000116698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:183472390..183472692 26863196 MeRIP-seq:(Medium) rs1247018061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221439,Human_RBP_ID_18969384,Human_RBP_ID_19039846,Human_RBP_ID_19442867,Human_RBP_ID_22871872,Human_RBP_ID_27801198 Human_Splice_Rec_165269,Human_Splice_Rec_165283,Human_Splice_Rec_165329,Human_Splice_Rec_165341,Human_Splice_Rec_165383,Human_Splice_Rec_165391,Human_Splice_Rec_165421,Human_Splice_Rec_165463,Human_Splice_Rec_165507,Human_Splice_Rec_165549,Human_Splice_Rec_165553 RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267 69428 RMVar_ID_69428 Human_SNP_ID_41559902 m1A Human chr1 + 183472887 183472887 183472887 GGCGAAGCCGGCTCGTCCCGGTGCGAGGAGGGAGGTTGGGGAAGCGTGAGAATGTGCGCGCGCGC GGCGAAGCCGGCTCGTCCCGGTGCGAGGAGGGGGGTTGGGGAAGCGTGAGAATGTGCGCGCGCGC A G SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:183472880..183473135 26863196 MeRIP-seq:(Medium) rs1016015899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9320291,Human_RBP_ID_23350381 RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267 69429 RMVar_ID_69429 Human_SNP_ID_41597816 m1A Human chr1 + 183630618 183630618 183630618 CATTAGCTTTAAAAGAGATGAGCACCTTCAAGACAATGCTGCCTGCCCGGTCCTGGTGGGTCAAT CATTAGCTTTAAAAGAGATGAGCACCTTCAAGGCAATGCTGCCTGCCCGGTCCTGGTGGGTCAAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:183630569..183630678 26863196 MeRIP-seq:(Medium) rs763930149 Functional Loss SNV dbSNP153 33..33 33 - - - 69430 RMVar_ID_69430 Human_SNP_ID_41597820 m1A Human chr1 - 183630636 183630636 183630636 CTAAATGTTCTGTTATTTATTGACCCACCAGGACCGGGCAGGCAGCATTGTCTTGAAGGTGCTCA CTAAATGTTCTGTTATTTATTGACCCACCAGGCCCGGGCAGGCAGCATTGTCTTGAAGGTGCTCA T G ARPC5 Ensembl:ENSG00000162704 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:183630501..183630708;chr1:183630458..183630708 26863196 MeRIP-seq:(Medium) rs78227740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853113,Human_RBP_ID_4012594,Human_RBP_ID_5726637,Human_RBP_ID_9357299 Human_Splice_Rec_165724,Human_Splice_Rec_165728,Human_Splice_Rec_165732,Human_Splice_Rec_165736 RMVar_hsa_circ_114889,RMVar_hsa_circ_123196,RMVar_hsa_circ_104611,RMVar_hsa_circ_138293,RMVar_hsa_circ_138295,RMVar_hsa_circ_81044,RMVar_hsa_circ_138294,RMVar_hsa_circ_138292 69431 RMVar_ID_69431 Human_SNP_ID_41598426 m1A Human chr1 - 183633099 183633099 183633099 AGGCAGCTCTGAAGAACCCCCCTATCAACACCAAGAGTCAGGCAGTGAAGGTGAGTCGCAGACTA AGGCAGCTCTGAAGAACCCCCCTATCAACACCCAGAGTCAGGCAGTGAAGGTGAGTCGCAGACTA T G ARPC5 Ensembl:ENSG00000162704 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:183633076..183633100 32194978 MeRIP-seq:(Medium) rs1558122785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853114,Human_RBP_ID_973441,Human_RBP_ID_1731427,Human_RBP_ID_8292640,Human_RBP_ID_8959894,Human_RBP_ID_10692359,Human_RBP_ID_18204634,Human_RBP_ID_19039857,Human_RBP_ID_22486573,Human_RBP_ID_27392002 Human_Splice_Rec_165723,Human_Splice_Rec_165727,Human_Splice_Rec_165731,Human_Splice_Rec_165735 Human_miRNA_ID_2453228 RMVar_hsa_circ_114889,RMVar_hsa_circ_123196,RMVar_hsa_circ_138293,RMVar_hsa_circ_138295,RMVar_hsa_circ_81044,RMVar_hsa_circ_138294 69432 RMVar_ID_69432 Human_SNP_ID_41599184 m1A Human chr1 - 183635645 183635645 183635645 CCGCTGGTCGGGATTGGGATGTCGAAGAACACAGTGTCGTCGGCCCGCTTCCGGAAGGTGGACGT CCGCTGGTCGGGATTGGGATGTCGAAGAACACGGTGTCGTCGGCCCGCTTCCGGAAGGTGGACGT T C ARPC5 Ensembl:ENSG00000162704 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:183635501..183635750;chr1:183635501..183635725 32194978 MeRIP-seq:(Medium) rs776545813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335363,Human_RBP_ID_743908,Human_RBP_ID_859823,Human_RBP_ID_1439125,Human_RBP_ID_4012603,Human_RBP_ID_5456762,Human_RBP_ID_5726655,Human_RBP_ID_8292641,Human_RBP_ID_9357302,Human_RBP_ID_10692395,Human_RBP_ID_18415120,Human_RBP_ID_22132357,Human_RBP_ID_22851216,Human_RBP_ID_23350653,Human_RBP_ID_26312325,Human_RBP_ID_26848598,Human_RBP_ID_27801199 RMVar_hsa_circ_138295,RMVar_hsa_circ_81044 69433 RMVar_ID_69433 Human_SNP_ID_41599185 m1A Human chr1 - 183635645 183635645 183635645 CCGCTGGTCGGGATTGGGATGTCGAAGAACACAGTGTCGTCGGCCCGCTTCCGGAAGGTGGACGT CCGCTGGTCGGGATTGGGATGTCGAAGAACACCGTGTCGTCGGCCCGCTTCCGGAAGGTGGACGT T G ARPC5 Ensembl:ENSG00000162704 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:183635501..183635750;chr1:183635501..183635725 32194978 MeRIP-seq:(Medium) rs776545813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335363,Human_RBP_ID_743908,Human_RBP_ID_859823,Human_RBP_ID_1439125,Human_RBP_ID_4012603,Human_RBP_ID_5456762,Human_RBP_ID_5726655,Human_RBP_ID_8292641,Human_RBP_ID_9357302,Human_RBP_ID_10692395,Human_RBP_ID_18415120,Human_RBP_ID_22132357,Human_RBP_ID_22851216,Human_RBP_ID_23350653,Human_RBP_ID_26312325,Human_RBP_ID_26848598,Human_RBP_ID_27801199 RMVar_hsa_circ_138295,RMVar_hsa_circ_81044 69434 RMVar_ID_69434 Human_SNP_ID_41599200 m1A Human chr1 - 183635689 183635689 183635689 GCTGGGCTTGCTGAGGTAGAGGCAGCGCCAAGAAGAGGCCTTTGCCGCTGGTCGGGATTGGGATG GCTGGGCTTGCTGAGGTAGAGGCAGCGCCAAGGAGAGGCCTTTGCCGCTGGTCGGGATTGGGATG T C ARPC5 Ensembl:ENSG00000162704 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:183635588..183635854 26863196 MeRIP-seq:(Medium) rs1304556141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335363,Human_RBP_ID_743909,Human_RBP_ID_1345805,Human_RBP_ID_4012603,Human_RBP_ID_5726656,Human_RBP_ID_9357302,Human_RBP_ID_10692395,Human_RBP_ID_18415120,Human_RBP_ID_22486575,Human_RBP_ID_23350653 RMVar_hsa_circ_138295,RMVar_hsa_circ_81044 69435 RMVar_ID_69435 Human_SNP_ID_41599204 m1A Human chr1 - 183635692 183635692 183635692 TGGGCTGGGCTTGCTGAGGTAGAGGCAGCGCCAAGAAGAGGCCTTTGCCGCTGGTCGGGATTGGG TGGGCTGGGCTTGCTGAGGTAGAGGCAGCGCCCAGAAGAGGCCTTTGCCGCTGGTCGGGATTGGG T G ARPC5 Ensembl:ENSG00000162704 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:183635647..183635741 26863410 MeRIP-seq:(Medium) rs1251673041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335365,Human_RBP_ID_743909,Human_RBP_ID_4012603,Human_RBP_ID_9357302,Human_RBP_ID_18415120,Human_RBP_ID_22486575,Human_RBP_ID_23350655 RMVar_hsa_circ_138295,RMVar_hsa_circ_81044 69436 RMVar_ID_69436 Human_SNP_ID_41599216 m1A Human chr1 + 183635710 183635710 183635710 CAAAGGCCTCTTCTTGGCGCTGCCTCTACCTCAGCAAGCCCAGCCCAGCAACCCACTACCCGGCG CAAAGGCCTCTTCTTGGCGCTGCCTCTACCTCGGCAAGCCCAGCCCAGCAACCCACTACCCGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:183635460..183635900;chr1:183635701..183635725;chr1:183633949..183635925;chr1:183635451..183635925;chr1:183633949..183635900 26863196 MeRIP-seq:(Medium) rs1486281350 Functional Loss SNV dbSNP153 33..33 33 - - - 69437 RMVar_ID_69437 Human_SNP_ID_41693374 m1A Human chr1 + 184051795 184051795 184051795 AGCGCGGCGATTCCGAGCCGACCCCCGGCTGCAGCGGCCTGGGTCCGGGCGGTGTTCGCGGCTTT AGCGCGGCGATTCCGAGCCGACCCCCGGCTGCGGCGGCCTGGGTCCGGGCGGTGTTCGCGGCTTT A G TSEN15 Ensembl:ENSG00000198860 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:184051750..184051842 26863196 MeRIP-seq:(Medium) rs759083409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074645,Human_RBP_ID_5311906,Human_RBP_ID_9319283 Human_Splice_Rec_165877,Human_Splice_Rec_165883,Human_Splice_Rec_165891,Human_Splice_Rec_165901,Human_Splice_Rec_165907,Human_Splice_Rec_165915,Human_Splice_Rec_165921,Human_Splice_Rec_165927,Human_Splice_Rec_165935,Human_Splice_Rec_165943,Human_Splice_Rec_165951,Human_Splice_Rec_165959,Human_Splice_Rec_165969,Human_Splice_Rec_165977,Human_Splice_Rec_165987,Human_Splice_Rec_165995,Human_Splice_Rec_166001 69438 RMVar_ID_69438 Human_SNP_ID_41696109 m1A Human chr1 + 184064323 184064322 184064323 ATGGGAATGGATGCCCTGGTTAAAGTAATAACATGAGCAAGGTATTGAGGGCTGAGAGGGCCTGA ATGGGAATGGATGCCCTGGTTAAAGTAATAAC_TGAGCAAGGTATTGAGGGCTGAGAGGGCCTGA CA C TSEN15 Ensembl:ENSG00000198860 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:184064321..184064596 26863196 MeRIP-seq:(Medium) rs1484941730 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10692716 RMVar_hsa_circ_138318,RMVar_hsa_circ_369266 69439 RMVar_ID_69439 Human_SNP_ID_41696132 m1A Human chr1 - 184064449 184064449 184064449 TTGTATCACACATACTCACTCCTTCTCCACCCATGCCACACCAATCTAGGGCTTTCTCACCAACT TTGTATCACACATACTCACTCCTTCTCCACCCGTGCCACACCAATCTAGGGCTTTCTCACCAACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:184064336..184064593 26863196 MeRIP-seq:(Medium) rs1246330506 Functional Loss SNV dbSNP153 33..33 33 - - - 69440 RMVar_ID_69440 Human_SNP_ID_41703773 m1A Human chr1 + 184099476 184099476 184099476 GGGGAAGTGAAGCCTCAATGGGTAGTGGCAGGAGACAGGCTGAAATCATGCAAGACCTGGTAAGT GGGGAAGTGAAGCCTCAATGGGTAGTGGCAGGCGACAGGCTGAAATCATGCAAGACCTGGTAAGT A C TSEN15 Ensembl:ENSG00000198860 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:184099399..184099483 26863196 MeRIP-seq:(Medium) rs1182068322 Functional Loss SNV dbSNP153 33..33 33 - - - 69441 RMVar_ID_69441 Human_SNP_ID_41772872 m1A Human chr1 + 184387267 184387264 184387267 GGAGGAGGGGGAGCCCCGGACACACTGTGGGGAGGAGGAGGAAGAAGAGGAGGAGGGAGGAAGAA GGAGGAGGGGGAGCCCCGGACACACTGTGG___GGAGGAGGAAGAAGAGGAGGAGGGAGGAAGAA GGGA G C1orf21 Ensembl:ENSG00000116667 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:184387069..184387308 26863196 MeRIP-seq:(Medium) rs1235977888 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_335441,Human_RBP_ID_4012725,Human_RBP_ID_5433307 69442 RMVar_ID_69442 Human_SNP_ID_41856848 m1A Human chr1 - 184754593 184754593 184754593 GGCTGTGGGTCCCCGGTTCCCCAGCGAGCGCGATGGAGACTAGTGGCGGCGACGGCCGCGTTCTG GGCTGTGGGTCCCCGGTTCCCCAGCGAGCGCGGTGGAGACTAGTGGCGGCGACGGCCGCGTTCTG T C EDEM3 Ensembl:ENSG00000116406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:184754546..184754628 26863196 MeRIP-seq:(Medium) rs761346445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073206,Human_RBP_ID_5312775,Human_RBP_ID_8754285 69443 RMVar_ID_69443 Human_SNP_ID_41856886 m1A Human chr1 - 184754646 184754646 184754646 TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCATGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCTTGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC T A EDEM3 Ensembl:ENSG00000116406 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:184754599..184754808 26863196 MeRIP-seq:(Medium) rs1234630372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223664,Human_RBP_ID_4073206,Human_RBP_ID_9270506,Human_RBP_ID_22428761 69444 RMVar_ID_69444 Human_SNP_ID_41856887 m1A Human chr1 - 184754646 184754646 184754646 TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCATGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCGTGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC T C EDEM3 Ensembl:ENSG00000116406 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:184754599..184754808 26863196 MeRIP-seq:(Medium) rs1234630372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223664,Human_RBP_ID_4073206,Human_RBP_ID_9270506,Human_RBP_ID_22428761 69445 RMVar_ID_69445 Human_SNP_ID_41856888 m1A Human chr1 - 184754646 184754646 184754646 TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCATGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCCTGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC T G EDEM3 Ensembl:ENSG00000116406 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:184754599..184754808 26863196 MeRIP-seq:(Medium) rs1234630372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223664,Human_RBP_ID_4073206,Human_RBP_ID_9270506,Human_RBP_ID_22428761 69446 RMVar_ID_69446 Human_SNP_ID_41866378 m1A Human chr1 - 184795156 184795156 184795156 CTGAGGAACAAGAAGAGATGGGAGGGCAAAGCAGCGCGGCCCAGGCCACGGCCAGTGTGAATGCA CTGAGGAACAAGAAGAGATGGGAGGGCAAAGCGGCGCGGCCCAGGCCACGGCCAGTGTGAATGCA T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:184795057..184795570;chr1:184794989..184795438 26863196 MeRIP-seq:(Medium) rs964730524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1558 Human_miRNA_ID_2026934 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 69447 RMVar_ID_69447 Human_SNP_ID_41866555 m1A Human chr1 - 184795499 184795499 184795499 GAAGAAGAAGAGGAAAAAGAGCCCAGTCAGGCAGCTGCCATCCACCCCGACAACTGTGAAGAAAG GAAGAAGAAGAGGAAAAAGAGCCCAGTCAGGCGGCTGCCATCCACCCCGACAACTGTGAAGAAAG T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:184795451..184795556 26863196 MeRIP-seq:(Medium) rs1328793874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26312328 Human_miRNA_ID_158810,Human_miRNA_ID_2240135 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 69448 RMVar_ID_69448 Human_SNP_ID_41926293 m1A Human chr1 - 185045440 185045440 185045440 GGCCGGCGCTGCGGGGAGGGCGGGAAGGAGCGAGCGAGCGAGGGGCGGAGGCGCGGGACGAGGAC GGCCGGCGCTGCGGGGAGGGCGGGAAGGAGCGGGCGAGCGAGGGGCGGAGGCGCGGGACGAGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:185045392..185045512 26863196 MeRIP-seq:(Medium) rs1350678445 Functional Loss SNV dbSNP153 33..33 33 - - - 69449 RMVar_ID_69449 Human_SNP_ID_41926298 m1A Human chr1 - 185045448 185045448 185045448 GCCGGCTCGGCCGGCGCTGCGGGGAGGGCGGGAAGGAGCGAGCGAGCGAGGGGCGGAGGCGCGGG GCCGGCTCGGCCGGCGCTGCGGGGAGGGCGGGGAGGAGCGAGCGAGCGAGGGGCGGAGGCGCGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:185045351..185046108 26863410 MeRIP-seq:(Medium) rs958831793 Functional Loss SNV dbSNP153 33..33 33 - - - 69450 RMVar_ID_69450 Human_SNP_ID_41926377 m1A Human chr1 - 185045636 185045636 185045636 CCCCGCCCGCCCCACTCACCGGCTCCTGCCCCAGCCCAGGGCTCCGCTGGCCGCGGCCGGAGCAA CCCCGCCCGCCCCACTCACCGGCTCCTGCCCCGGCCCAGGGCTCCGCTGGCCGCGGCCGGAGCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:185045586..185045715 26863196 MeRIP-seq:(Medium) rs1371047182 Functional Loss SNV dbSNP153 33..33 33 - - - 69451 RMVar_ID_69451 Human_SNP_ID_41954143 m1A Human chr1 + 185156890 185156890 185156890 ATGAAGAACCAGTGACCAAATCCTGTTAGTAGAAAACAGAAAGCCAGAGGCAGCGATTCCAGATG ATGAAGAACCAGTGACCAAATCCTGTTAGTAGCAAACAGAAAGCCAGAGGCAGCGATTCCAGATG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:185156841..185156912 26863196 MeRIP-seq:(Medium) rs1439142134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10695960 69452 RMVar_ID_69452 Human_SNP_ID_41954144 m1A Human chr1 + 185156890 185156890 185156890 ATGAAGAACCAGTGACCAAATCCTGTTAGTAGAAAACAGAAAGCCAGAGGCAGCGATTCCAGATG ATGAAGAACCAGTGACCAAATCCTGTTAGTAGGAAACAGAAAGCCAGAGGCAGCGATTCCAGATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:185156841..185156912 26863196 MeRIP-seq:(Medium) rs1439142134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10695960 69453 RMVar_ID_69453 Human_SNP_ID_41954145 m1A Human chr1 + 185156890 185156890 185156890 ATGAAGAACCAGTGACCAAATCCTGTTAGTAGAAAACAGAAAGCCAGAGGCAGCGATTCCAGATG ATGAAGAACCAGTGACCAAATCCTGTTAGTAGTAAACAGAAAGCCAGAGGCAGCGATTCCAGATG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:185156841..185156912 26863196 MeRIP-seq:(Medium) rs1439142134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10695960 69454 RMVar_ID_69454 Human_SNP_ID_41991384 m1A Human chr1 + 185311244 185311244 185311244 GTGTCTTAAGCTCTAATGGTGATTCCAAAACTATCAGGCTTGAAAATGATGTAATCAAGTCCTTA GTGTCTTAAGCTCTAATGGTGATTCCAAAACTCTCAGGCTTGAAAATGATGTAATCAAGTCCTTA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:185311226..185311250 26863196 MeRIP-seq:(Medium) rs558432484 Functional Loss SNV dbSNP153 33..33 33 - - - 69455 RMVar_ID_69455 Human_SNP_ID_41991385 m1A Human chr1 + 185311244 185311244 185311244 GTGTCTTAAGCTCTAATGGTGATTCCAAAACTATCAGGCTTGAAAATGATGTAATCAAGTCCTTA GTGTCTTAAGCTCTAATGGTGATTCCAAAACTGTCAGGCTTGAAAATGATGTAATCAAGTCCTTA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:185311226..185311250 26863196 MeRIP-seq:(Medium) rs558432484 Functional Loss SNV dbSNP153 33..33 33 - - - 69456 RMVar_ID_69456 Human_SNP_ID_41992395 m1A Human chr1 - 185316194 185316194 185316194 TGCGGAGTGGGCGCCGGCCTGGCTGCGCGAGGAGGAAGGCCTGGGACGCTCTTTCTTTTTTATGA TGCGGAGTGGGCGCCGGCCTGGCTGCGCGAGGGGGAAGGCCTGGGACGCTCTTTCTTTTTTATGA T C IVNS1ABP Ensembl:ENSG00000116679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:185316190..185316311;chr1:185316192..185316294 26863196 MeRIP-seq:(Medium) rs1250030423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5729304,Human_RBP_ID_10697033,Human_RBP_ID_17103758 69457 RMVar_ID_69457 Human_SNP_ID_42233691 m1A Human chr1 + 186307137 186307137 186307137 CACTCCCAAGGAGCCTGCACCCACCACCAAGGAGCCTGCACCCACCACTCCCAAAGAGCCTGCAC CACTCCCAAGGAGCCTGCACCCACCACCAAGGGGCCTGCACCCACCACTCCCAAAGAGCCTGCAC A G PRG4 Ensembl:ENSG00000116690 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:186307062..186307366 26863196 MeRIP-seq:(Medium) rs756169288 Functional Loss SNV dbSNP153 33..33 33 - - - 69458 RMVar_ID_69458 Human_SNP_ID_42233699 m1A Human chr1 + 186307148 186307145 186307148 AGCCTGCACCCACCACCAAGGAGCCTGCACCCACCACTCCCAAAGAGCCTGCACCCACTGCCCCC AGCCTGCACCCACCACCAAGGAGCCTGCAC___CCACTCCCAAAGAGCCTGCACCCACTGCCCCC CCCA C PRG4 Ensembl:ENSG00000116690 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:186307100..186307369 26863196 MeRIP-seq:(Medium) rs778276376 Functional Loss DEL dbSNP153 31..33 33 - - - 69459 RMVar_ID_69459 Human_SNP_ID_42233700 m1A Human chr1 + 186307148 186307148 186307148 AGCCTGCACCCACCACCAAGGAGCCTGCACCCACCACTCCCAAAGAGCCTGCACCCACTGCCCCC AGCCTGCACCCACCACCAAGGAGCCTGCACCCTCCACTCCCAAAGAGCCTGCACCCACTGCCCCC A T PRG4 Ensembl:ENSG00000116690 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:186307100..186307369 26863196 MeRIP-seq:(Medium) rs746751838 Functional Loss SNV dbSNP153 33..33 33 - - - 69460 RMVar_ID_69460 Human_SNP_ID_42233948 m1A Human chr1 + 186307515 186307492 186307516 TCCCAAGGAACCTGCACCCACCACCACCAAGAAGCCTGCACCCACCACTCCCAAAGAGCCTGCCC TCCCAAGGAA________________________CCTGCACCCACCACTCCCAAAGAGCCTGCCC ACCTGCACCCACCACCACCAAGAAG A PRG4 Ensembl:ENSG00000116690 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:186307432..186307561 26863196 MeRIP-seq:(Medium) rs770908491 Functional Loss DEL dbSNP153 11..34 33 - - - 69461 RMVar_ID_69461 Human_SNP_ID_42233979 m1A Human chr1 + 186307537 186307537 186307537 ACCACCAAGAAGCCTGCACCCACCACTCCCAAAGAGCCTGCCCCAACTACCCCCAAGGAGACTGC ACCACCAAGAAGCCTGCACCCACCACTCCCAAGGAGCCTGCCCCAACTACCCCCAAGGAGACTGC A G PRG4 Ensembl:ENSG00000116690 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:186307486..186307572 26863196 MeRIP-seq:(Medium) rs769259991 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 69462 RMVar_ID_69462 Human_SNP_ID_42239148 m1A Human chr1 - 186326201 186326201 186326201 TTATGAAGAGGATGAGGAAGATGATGATGATGATGAAGATGACACAGGGATGGGAGATGAGGGTG TTATGAAGAGGATGAGGAAGATGATGATGATGCTGAAGATGACACAGGGATGGGAGATGAGGGTG T G TPR Ensembl:ENSG00000047410 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:186326057..186326286 26863196 MeRIP-seq:(Medium) rs966473045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1559,Human_RBP_ID_800818,Human_RBP_ID_855604,Human_RBP_ID_1731708,Human_RBP_ID_2181381,Human_RBP_ID_4013275,Human_RBP_ID_5536959,Human_RBP_ID_5729562,Human_RBP_ID_8754292,Human_RBP_ID_9253083,Human_RBP_ID_9270514,Human_RBP_ID_9357309,Human_RBP_ID_9474426,Human_RBP_ID_10697419,Human_RBP_ID_17763041,Human_RBP_ID_18409981,Human_RBP_ID_18522800,Human_RBP_ID_18558364,Human_RBP_ID_22026517,Human_RBP_ID_22781529,Human_RBP_ID_22871007,Human_RBP_ID_23112465,Human_RBP_ID_23351552,Human_RBP_ID_24541297,Human_RBP_ID_24617005,Human_RBP_ID_26312347,Human_RBP_ID_26848742,Human_RBP_ID_27798961 Human_Splice_Rec_167146,Human_Splice_Rec_167147,Human_Splice_Rec_167175 RMVar_hsa_circ_3700,RMVar_hsa_circ_78732,RMVar_hsa_circ_99079,RMVar_hsa_circ_103104,RMVar_hsa_circ_138425,RMVar_hsa_circ_138427,RMVar_hsa_circ_64852,RMVar_hsa_circ_138426,RMVar_hsa_circ_105287,RMVar_hsa_circ_123634,RMVar_hsa_circ_138430,RMVar_hsa_circ_365187,RMVar_hsa_circ_98048,RMVar_hsa_circ_120750,RMVar_hsa_circ_49811,RMVar_hsa_circ_93366,RMVar_hsa_circ_109808,RMVar_hsa_circ_115367,RMVar_hsa_circ_138432,RMVar_hsa_circ_138433,RMVar_hsa_circ_138434,RMVar_hsa_circ_114854,RMVar_hsa_circ_138438,RMVar_hsa_circ_94228,RMVar_hsa_circ_106047,RMVar_hsa_circ_138439,RMVar_hsa_circ_138436,RMVar_hsa_circ_138437,RMVar_hsa_circ_138435,RMVar_hsa_circ_123351,RMVar_hsa_circ_82197,RMVar_hsa_circ_138440,RMVar_hsa_circ_138441,RMVar_hsa_circ_353475,RMVar_hsa_circ_59013,RMVar_hsa_circ_72903,RMVar_hsa_circ_138445,RMVar_hsa_circ_37852,RMVar_hsa_circ_138442,RMVar_hsa_circ_138443,RMVar_hsa_circ_138444,RMVar_hsa_circ_370096 69463 RMVar_ID_69463 Human_SNP_ID_42239995 m1A Human chr1 + 186327398 186327398 186327398 ACCAGAATTTACAGCCAATGCATTAGTATCCCAAGGATTTGAGCACTTTCATCCAATAGTTTAAA ACCAGAATTTACAGCCAATGCATTAGTATCCCTAGGATTTGAGCACTTTCATCCAATAGTTTAAA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:186327396..186327575 26863196 MeRIP-seq:(Medium) rs933326255 Functional Loss SNV dbSNP153 33..33 33 - - - 69464 RMVar_ID_69464 Human_SNP_ID_42241761 m1A Human chr1 - 186334330 186334330 186334330 TACAGTGATGCCCACTACACAAGTGGAATCACAGGAAGGTTAGTAAAATAATACAGATCTGATGA TACAGTGATGCCCACTACACAAGTGGAATCACTGGAAGGTTAGTAAAATAATACAGATCTGATGA T A TPR Ensembl:ENSG00000047410 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs769916058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17221850,Human_RBP_ID_26848758 Human_Splice_Rec_167137 RMVar_hsa_circ_78732,RMVar_hsa_circ_99079,RMVar_hsa_circ_103104,RMVar_hsa_circ_138425,RMVar_hsa_circ_138427,RMVar_hsa_circ_64852,RMVar_hsa_circ_138426,RMVar_hsa_circ_105287,RMVar_hsa_circ_123634,RMVar_hsa_circ_138430,RMVar_hsa_circ_98048,RMVar_hsa_circ_120750,RMVar_hsa_circ_49811,RMVar_hsa_circ_93366,RMVar_hsa_circ_109808,RMVar_hsa_circ_115367,RMVar_hsa_circ_138432,RMVar_hsa_circ_138433,RMVar_hsa_circ_138434,RMVar_hsa_circ_114854,RMVar_hsa_circ_138438,RMVar_hsa_circ_106047,RMVar_hsa_circ_138439,RMVar_hsa_circ_138436,RMVar_hsa_circ_138437,RMVar_hsa_circ_123351,RMVar_hsa_circ_82197,RMVar_hsa_circ_138440,RMVar_hsa_circ_138441,RMVar_hsa_circ_353475,RMVar_hsa_circ_59013,RMVar_hsa_circ_72903,RMVar_hsa_circ_69062,RMVar_hsa_circ_138445,RMVar_hsa_circ_37852,RMVar_hsa_circ_138442,RMVar_hsa_circ_138443,RMVar_hsa_circ_138444,RMVar_hsa_circ_370096,RMVar_hsa_circ_34212,RMVar_hsa_circ_55295 69465 RMVar_ID_69465 Human_SNP_ID_42247898 m1A Human chr1 - 186357018 186357018 186357018 CTATGTGTTCCTAACAGTGCTAGATACTTGGGATATAGTGATATAGGGAGGAAAGAATTGAGCAA CTATGTGTTCCTAACAGTGCTAGATACTTGGGGTATAGTGATATAGGGAGGAAAGAATTGAGCAA T C TPR Ensembl:ENSG00000047410 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:186356343..186357502 32194978 MeRIP-seq:(Medium) rs1050006040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1731792,Human_RBP_ID_3290473,Human_RBP_ID_9474537,Human_RBP_ID_10697934,Human_RBP_ID_23351624 RMVar_hsa_circ_99079,RMVar_hsa_circ_138425,RMVar_hsa_circ_109808,RMVar_hsa_circ_138438,RMVar_hsa_circ_106047,RMVar_hsa_circ_138439,RMVar_hsa_circ_353475,RMVar_hsa_circ_60833,RMVar_hsa_circ_18804,RMVar_hsa_circ_57944,RMVar_hsa_circ_42661,RMVar_hsa_circ_25228,RMVar_hsa_circ_78155,RMVar_hsa_circ_92134,RMVar_hsa_circ_121294,RMVar_hsa_circ_138451,RMVar_hsa_circ_82716,RMVar_hsa_circ_138454,RMVar_hsa_circ_138456,RMVar_hsa_circ_138455,RMVar_hsa_circ_138452,RMVar_hsa_circ_138453 69466 RMVar_ID_69466 Human_SNP_ID_42248877 m1A Human chr1 + 186360827 186360827 186360827 TTGCATTCTCTAATTCCTTCTCCAATCTCCCTATTTTCTCAAGCATTTCTTTTTCCATTTGATCT TTGCATTCTCTAATTCCTTCTCCAATCTCCCTGTTTTCTCAAGCATTTCTTTTTCCATTTGATCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:186360344..186360845 32194978 MeRIP-seq:(Medium) rs199892357 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_284 69467 RMVar_ID_69467 Human_SNP_ID_42252728 m1A Human chr1 + 186375168 186375168 186375168 CGCTCGGTGGCTCGCGCGCGCCCGCCCGCCGGAGACTCCCGCGGCGGGACCCTGGGAAATCGAGT CGCTCGGTGGCTCGCGCGCGCCCGCCCGCCGGGGACTCCCGCGGCGGGACCCTGGGAAATCGAGT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:186375076..186375225 26863410 MeRIP-seq:(Medium) rs1205764373 Functional Loss SNV dbSNP153 33..33 33 - - - 69468 RMVar_ID_69468 Human_SNP_ID_42328103 m1A Human chr1 + 186680304 186680304 186680304 GCAGGGCGCGGGCGAGCATCGCAGCGGCGGGCAGGGCGCGGCGCGGGGGTAGGCTTTGCTGTCTG GCAGGGCGCGGGCGAGCATCGCAGCGGCGGGCGGGGCGCGGCGCGGGGGTAGGCTTTGCTGTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:186680265..186680346 26863196 MeRIP-seq:(Medium) rs1341205474 Functional Loss SNV dbSNP153 33..33 33 - - - 69469 RMVar_ID_69469 Human_SNP_ID_43901259 m1A Human chr1 + 192809101 192809101 192809101 ATAATGCAAAGTGCTATGTTCTTGGCTGTTCAACACGACTGCAGACCCATGGACAAGAGCGCAGG ATAATGCAAAGTGCTATGTTCTTGGCTGTTCAGCACGACTGCAGACCCATGGACAAGAGCGCAGG A G RGS2 Ensembl:ENSG00000116741 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:192809051..192809200 26863196 MeRIP-seq:(Medium) rs762913377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1417493,Human_RBP_ID_5456806 Human_Splice_Rec_167989,Human_Splice_Rec_167991,Human_Splice_Rec_167999,Human_Splice_Rec_168003 69470 RMVar_ID_69470 Human_SNP_ID_43902107 m1A Human chr1 + 192812129 192812129 192812129 TAAAACTGAAATGGTCCGTGTTTGCATTGTTAAAAATGATGTGTGAAATAGAATGAGTGCTATGG TAAAACTGAAATGGTCCGTGTTTGCATTGTTAGAAATGATGTGTGAAATAGAATGAGTGCTATGG A G RGS2 Ensembl:ENSG00000116741 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:192812079..192812182 26863196 MeRIP-seq:(Medium) rs979150183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_335967,Human_RBP_ID_18558574,Human_RBP_ID_23352150 69471 RMVar_ID_69471 Human_SNP_ID_43902110 m1A Human chr1 - 192812138 192812138 192812138 TTTTCAACACCATAGCACTCATTCTATTTCACACATCATTTTTAACAATGCAAACACGGACCATT TTTTCAACACCATAGCACTCATTCTATTTCACGCATCATTTTTAACAATGCAAACACGGACCATT T C AL390957.1 Ensembl:ENSG00000285280 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:192812088..192812185 26863196 MeRIP-seq:(Medium) rs1215699294 Functional Loss SNV dbSNP153 33..33 33 - - - 69472 RMVar_ID_69472 Human_SNP_ID_43956867 m1A Human chr1 - 193051756 193051756 193051756 TGGAGTTTAGAGCCTGAGAATTTTGAAAAATTAAAGTAAGTATAATTTTAGTTGTGTTAATATGT TGGAGTTTAGAGCCTGAGAATTTTGAAAAATTGAAGTAAGTATAATTTTAGTTGTGTTAATATGT T C UCHL5 Ensembl:ENSG00000116750 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:193051751..193051775 32194978 MeRIP-seq:(Medium) rs200637687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3937102,Human_RBP_ID_10704707,Human_RBP_ID_18558648,Human_RBP_ID_18969400,Human_RBP_ID_22873313,Human_RBP_ID_23352476,Human_RBP_ID_26312431 Human_Splice_Rec_168012,Human_Splice_Rec_168013,Human_Splice_Rec_168048,Human_Splice_Rec_168049,Human_Splice_Rec_168076,Human_Splice_Rec_168077,Human_Splice_Rec_168098,Human_Splice_Rec_168099,Human_Splice_Rec_168120,Human_Splice_Rec_168121,Human_Splice_Rec_168142,Human_Splice_Rec_168143,Human_Splice_Rec_168180,Human_Splice_Rec_168181,Human_Splice_Rec_168196,Human_Splice_Rec_168197,Human_Splice_Rec_168202 RMVar_hsa_circ_6337,RMVar_hsa_circ_73412,RMVar_hsa_circ_363098 69473 RMVar_ID_69473 Human_SNP_ID_43958446 m1A Human chr1 - 193059293 193059293 193059293 GCGGCAGCTGGTGCGGGGGGCAGCTGAGAGCGAGAGGTGGATCGGGGCGGTGTGTGGCCAGGGCC GCGGCAGCTGGTGCGGGGGGCAGCTGAGAGCGGGAGGTGGATCGGGGCGGTGTGTGGCCAGGGCC T C UCHL5 Ensembl:ENSG00000116750 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:193051776..193059732;chr1:193059197..193059375;chr1:193059084..193059716;chr1:193049751..193059465;chr1:193059131..193059563 26863196 MeRIP-seq:(Medium) rs571763646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223707,Human_RBP_ID_3937104,Human_RBP_ID_4013791,Human_RBP_ID_5311912,Human_RBP_ID_5413343,Human_RBP_ID_5433339,Human_RBP_ID_5731924,Human_RBP_ID_9320298,Human_RBP_ID_18429150,Human_RBP_ID_22871873,Human_RBP_ID_26312432,Human_RBP_ID_26849000 69474 RMVar_ID_69474 Human_SNP_ID_43958447 m1A Human chr1 - 193059293 193059293 193059293 GCGGCAGCTGGTGCGGGGGGCAGCTGAGAGCGAGAGGTGGATCGGGGCGGTGTGTGGCCAGGGCC GCGGCAGCTGGTGCGGGGGGCAGCTGAGAGCGCGAGGTGGATCGGGGCGGTGTGTGGCCAGGGCC T G UCHL5 Ensembl:ENSG00000116750 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:193051776..193059732;chr1:193059197..193059375;chr1:193059084..193059716;chr1:193049751..193059465;chr1:193059131..193059563 26863196 MeRIP-seq:(Medium) rs571763646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223707,Human_RBP_ID_3937104,Human_RBP_ID_4013791,Human_RBP_ID_5311912,Human_RBP_ID_5413343,Human_RBP_ID_5433339,Human_RBP_ID_5731924,Human_RBP_ID_9320298,Human_RBP_ID_18429150,Human_RBP_ID_22871873,Human_RBP_ID_26312432,Human_RBP_ID_26849000 69475 RMVar_ID_69475 Human_SNP_ID_43969691 m1A Human chr1 - 193105278 193105269 193105278 GACAGGGCGGCGGGAGCTGCGGGAGCTGCGGCAGCTGCGGCCTCTGGGTACGGGGTCAGCGGGCA GACAGGGCGGCGGGAGCTGCGGGAGCTGCGGC_________CTCTGGGTACGGGGTCAGCGGGCA GGCCGCAGCT G GLRX2 Ensembl:ENSG00000023572 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:193101170..193105465 26863196 MeRIP-seq:(Medium) rs753977238 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_746089,Human_RBP_ID_4074672,Human_RBP_ID_5312782,Human_RBP_ID_19035798 Human_Splice_Rec_168341,Human_Splice_Rec_168347 69476 RMVar_ID_69476 Human_SNP_ID_43969748 m1A Human chr1 - 193105352 193105351 193105352 CCATGATTTGGCGCCGCGCGGCGCTGGCGGGGACGCGGCTGGTTTGGAGCAGGAGCGGCTCGGCA CCATGATTTGGCGCCGCGCGGCGCTGGCGGGG_CGCGGCTGGTTTGGAGCAGGAGCGGCTCGGCA GT G GLRX2 Ensembl:ENSG00000023572 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:193105271..193105397 26863196 MeRIP-seq:(Medium) rs772478431 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4074672,Human_RBP_ID_5312782 Human_Splice_Rec_168341,Human_Splice_Rec_168347 69477 RMVar_ID_69477 Human_SNP_ID_43969756 m1A Human chr1 + 193105360 193105360 193105360 CGCTCCTGCTCCAAACCAGCCGCGTCCCCGCCAGCGCCGCGCGGCGCCAAATCATGGTCAGAGCC CGCTCCTGCTCCAAACCAGCCGCGTCCCCGCCCGCGCCGCGCGGCGCCAAATCATGGTCAGAGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:193105141..193105430;chr1:193105143..193105565;chr1:193105163..193105425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 69478 RMVar_ID_69478 Human_SNP_ID_43974024 m1A Human chr1 + 193122130 193122130 193122130 CGGCGAAGGAGGAGGAGGAAGAGGGCGAGGCGACAAGAGAAGAAGGAGGCAGGCGCGGCGGCAGC CGGCGAAGGAGGAGGAGGAAGAGGGCGAGGCGGCAAGAGAAGAAGGAGGCAGGCGCGGCGGCAGC A G CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:193122076..193122250 26863196 MeRIP-seq:(Medium) rs963763476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803869,Human_RBP_ID_3937105,Human_RBP_ID_4086461,Human_RBP_ID_9319292,Human_RBP_ID_18468652,Human_RBP_ID_22871015,Human_RBP_ID_24541856,Human_RBP_ID_26312433,Human_RBP_ID_27799044 RMVar_hsa_circ_82886,RMVar_hsa_circ_138528 69479 RMVar_ID_69479 Human_SNP_ID_43974025 m1A Human chr1 + 193122133 193122133 193122133 CGAAGGAGGAGGAGGAAGAGGGCGAGGCGACAAGAGAAGAAGGAGGCAGGCGCGGCGGCAGCGGC CGAAGGAGGAGGAGGAAGAGGGCGAGGCGACAGGAGAAGAAGGAGGCAGGCGCGGCGGCAGCGGC A G CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:193121993..193122357 26863196 MeRIP-seq:(Medium) rs1222107185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803869,Human_RBP_ID_3937105,Human_RBP_ID_4086462,Human_RBP_ID_9319292,Human_RBP_ID_18468652,Human_RBP_ID_22871015,Human_RBP_ID_24541856,Human_RBP_ID_26312433,Human_RBP_ID_27799044 RMVar_hsa_circ_82886,RMVar_hsa_circ_138528 69480 RMVar_ID_69480 Human_SNP_ID_43974913 m1A Human chr1 + 193125044 193125044 193125044 AAACTCATTGTTGTTAGCAAAGTTGTTTATATAAATGAATCCAGCCTGAAGAGTTGAATTAGAAT AAACTCATTGTTGTTAGCAAAGTTGTTTATATGAATGAATCCAGCCTGAAGAGTTGAATTAGAAT A G CDC73 Ensembl:ENSG00000134371 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:193125043..193125175 26863196 MeRIP-seq:(Medium) rs1432219614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82886,RMVar_hsa_circ_138528 69481 RMVar_ID_69481 Human_SNP_ID_44009337 m1A Human chr1 - 193257469 193257469 193257469 CTCCTCATTTTAATGAATACCTCACCCTCTCTATCTCAGTTACTTCCAAGGTCTTGACTTTTTCT CTCCTCATTTTAATGAATACCTCACCCTCTCTCTCTCAGTTACTTCCAAGGTCTTGACTTTTTCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:193257255..193257581 26863196 MeRIP-seq:(Medium) rs538406696 Functional Loss SNV dbSNP153 33..33 33 - - - 69482 RMVar_ID_69482 Human_SNP_ID_44010062 m1A Human chr1 + 193260184 193260184 193260184 TAGGGAACAGGAGGTTTAAGGCAGGCAGGAACATACCTGCCATTTAAAGGACCATTAAGGAATCC TAGGGAACAGGAGGTTTAAGGCAGGCAGGAACCTACCTGCCATTTAAAGGACCATTAAGGAATCC A C lnc-CDC73-5 RNACentral:URS00008BB467 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:193260135..193260248 26863196 MeRIP-seq:(Medium) rs1185668222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138556 69483 RMVar_ID_69483 Human_SNP_ID_139271394 m1A Human chr3 + 75214626 75214626 75214626 CCGTCGCCGTCGCCGCCGGGGGGAGGAGGGCCATGATCCAAAGGAACCAGAGCAGTTGAGAAAAC CCGTCGCCGTCGCCGCCGGGGGGAGGAGGGCCGTGATCCAAAGGAACCAGAGCAGTTGAGAAAAC A G AC117481.1 Ensembl:ENSG00000287398 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:75214543..75214683 26863410 MeRIP-seq:(Medium) rs1462890396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608247,Human_RBP_ID_18010831 69484 RMVar_ID_69484 Human_SNP_ID_139328056 m1A Human chr3 - 75422379 75422379 75422379 CTGCAGAGGTCACAGGGAAGTCAGAGAACAGTAATACGCTAACAGGGGCACGGGGCATGAAGAAC CTGCAGAGGTCACAGGGAAGTCAGAGAACAGTCATACGCTAACAGGGGCACGGGGCATGAAGAAC T G FAM86DP Ensembl:ENSG00000244026 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:75422328..75422452 26863196 MeRIP-seq:(Medium) rs111516371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5603772,Human_RBP_ID_7237614 69485 RMVar_ID_69485 Human_SNP_ID_139880670 m1A Human chr3 - 77410526 77410512 77410526 GGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAGGAGGAGGAGGAAGAGGAGGAAGAGGAGGAGG GGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAG______________GAGGAGGAAGAGGAGGAGG CTTCCTCCTCCTCCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:77410503..77410574 26863196 MeRIP-seq:(Medium) rs1447848682 Functional Loss DEL dbSNP153 33..46 33 - - - 69486 RMVar_ID_69486 Human_SNP_ID_139880698 m1A Human chr3 - 77410543 77410533 77410543 GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAGGAGGAGGAGGAAGA GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGA__________GAGGAAGAGGAGGAGGAGGAAGA CCTCCTCTTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:77410481..77410589 26863196 MeRIP-seq:(Medium) rs1560757060 Functional Loss DEL dbSNP153 33..42 33 - - - 69487 RMVar_ID_69487 Human_SNP_ID_139880702 m1A Human chr3 - 77410543 77410537 77410543 GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAGGAGGAGGAGGAAGA GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGA______GGAGGAGGAAGAGGAGGAGGAGGAAGA CTCTTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:77410481..77410589 26863196 MeRIP-seq:(Medium) rs1483329015 Functional Loss DEL dbSNP153 33..38 33 - - - 69488 RMVar_ID_69488 Human_SNP_ID_139880707 m1A Human chr3 - 77410543 77410543 77410543 GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAGGAGGAGGAGGAAGA GAGGAGGAAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAGGAGGAGGAAGAGGAGGAGGAGGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:77410481..77410589 26863196 MeRIP-seq:(Medium) rs1466111796 Functional Loss SNV dbSNP153 33..33 33 - - - 69489 RMVar_ID_69489 Human_SNP_ID_140180789 m1A Human chr3 - 78597792 78597792 78597792 ATTTGGAATATTTGAATAATGACAGATGGTGAAGTAACATGCATACTTTATTGTGGGCCATGAAC ATTTGGAATATTTGAATAATGACAGATGGTGATGTAACATGCATACTTTATTGTGGGCCATGAAC T A ROBO1 Ensembl:ENSG00000169855 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7626143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1631595,Human_RBP_ID_1968725,Human_RBP_ID_5120796,Human_RBP_ID_8949766,Human_RBP_ID_22398921,Human_RBP_ID_26512199,Human_RBP_ID_27059184 GWAS_ID_8385,GWAS_ID_8386 69490 RMVar_ID_69490 Human_SNP_ID_140180790 m1A Human chr3 - 78597792 78597792 78597792 ATTTGGAATATTTGAATAATGACAGATGGTGAAGTAACATGCATACTTTATTGTGGGCCATGAAC ATTTGGAATATTTGAATAATGACAGATGGTGAGGTAACATGCATACTTTATTGTGGGCCATGAAC T C ROBO1 Ensembl:ENSG00000169855 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7626143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1631595,Human_RBP_ID_1968725,Human_RBP_ID_5120796,Human_RBP_ID_8949766,Human_RBP_ID_22398921,Human_RBP_ID_26512199,Human_RBP_ID_27059184 GWAS_ID_8385,GWAS_ID_8386 69491 RMVar_ID_69491 Human_SNP_ID_140180791 m1A Human chr3 - 78597792 78597792 78597792 ATTTGGAATATTTGAATAATGACAGATGGTGAAGTAACATGCATACTTTATTGTGGGCCATGAAC ATTTGGAATATTTGAATAATGACAGATGGTGACGTAACATGCATACTTTATTGTGGGCCATGAAC T G ROBO1 Ensembl:ENSG00000169855 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7626143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1631595,Human_RBP_ID_1968725,Human_RBP_ID_5120796,Human_RBP_ID_8949766,Human_RBP_ID_22398921,Human_RBP_ID_26512199,Human_RBP_ID_27059184 GWAS_ID_8385,GWAS_ID_8386 69492 RMVar_ID_69492 Human_SNP_ID_140229649 m1A Human chr3 - 78796625 78796625 78796625 ATTGAAGAGACTTGAAAGTAAATTGGTAGAGAACAGGATGTGGCACCACGGAATTAGGGGAAGTT ATTGAAGAGACTTGAAAGTAAATTGGTAGAGAGCAGGATGTGGCACCACGGAATTAGGGGAAGTT T C ROBO1 Ensembl:ENSG00000169855 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:78796621..78796698 26863196 MeRIP-seq:(Medium) rs911137182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86565,RMVar_hsa_circ_219767,RMVar_hsa_circ_309476,RMVar_hsa_circ_342781 69493 RMVar_ID_69493 Human_SNP_ID_140250057 m1A Human chr3 + 78882660 78882660 78882660 ACTCAATGTCAGTATATCCATCCTCAATTCCTATCTCTCCATCTTTCTCCTTTGCCTCCAGGTAT ACTCAATGTCAGTATATCCATCCTCAATTCCTCTCTCTCCATCTTTCTCCTTTGCCTCCAGGTAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:78882628..78882757 26863196 MeRIP-seq:(Medium) rs907701255 Functional Loss SNV dbSNP153 33..33 33 - - - 69494 RMVar_ID_69494 Human_SNP_ID_140253611 m1A Human chr3 + 78896380 78896380 78896380 GAAGATCCACAAAAGACGTGAAAATAGCCTTAACTGATGACATTCCACCATTGTAATTTGCTTCT GAAGATCCACAAAAGACGTGAAAATAGCCTTAGCTGATGACATTCCACCATTGTAATTTGCTTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:78896360..78896457 26863196 MeRIP-seq:(Medium) rs991228955 Functional Loss SNV dbSNP153 33..33 33 - - - 69495 RMVar_ID_69495 Human_SNP_ID_140284685 m1A Human chr3 - 79018963 79018963 79018963 CCTCCGGAGCTGCTGCTTCTACTTTGGCTGCTATCGCCGCCGCCGCGGGTGGCCCGCTGCTGACT CCTCCGGAGCTGCTGCTTCTACTTTGGCTGCTGTCGCCGCCGCCGCGGGTGGCCCGCTGCTGACT T C ROBO1 Ensembl:ENSG00000169855 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:79018914..79019120 26863196 MeRIP-seq:(Medium) rs1458271859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756599,Human_RBP_ID_5530588,Human_RBP_ID_18814940,Human_RBP_ID_22456057 RMVar_hsa_circ_76339,RMVar_hsa_circ_277905,RMVar_hsa_circ_219793 69496 RMVar_ID_69496 Human_SNP_ID_140284688 m1A Human chr3 + 79018972 79018972 79018972 CGGGCCACCCGCGGCGGCGGCGATAGCAGCCAAAGTAGAAGCAGCAGCTCCGGAGGAAGGGCTCG CGGGCCACCCGCGGCGGCGGCGATAGCAGCCACAGTAGAAGCAGCAGCTCCGGAGGAAGGGCTCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:79018921..79019555 26863196 MeRIP-seq:(Medium) rs1225596377 Functional Loss SNV dbSNP153 33..33 33 - - - 69497 RMVar_ID_69497 Human_SNP_ID_140284843 m1A Human chr3 - 79019417 79019417 79019417 GAGAGGAGGCAGCGTGAGAGCAGAAACTTCAGACGCCGCTGATCCGGGAGGAGCTGGGGTGAGCC GAGAGGAGGCAGCGTGAGAGCAGAAACTTCAGTCGCCGCTGATCCGGGAGGAGCTGGGGTGAGCC T A ROBO1 Ensembl:ENSG00000169855 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:79019226..79019450 26863196 MeRIP-seq:(Medium) rs1171662055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4767681,Human_RBP_ID_18424018 RMVar_hsa_circ_76339,RMVar_hsa_circ_277905,RMVar_hsa_circ_219793 69498 RMVar_ID_69498 Human_SNP_ID_140945511 m1A Human chr3 - 81591161 81591161 81591161 TATATCCGTATTGATTTTCTTTTTCTAAGGTCAAGGTTTCTCAGGTGATTACAGTGAATATTTCG TATATCCGTATTGATTTTCTTTTTCTAAGGTCCAGGTTTCTCAGGTGATTACAGTGAATATTTCG T G GBE1 Ensembl:ENSG00000114480 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:81591114..81594007 32194978 MeRIP-seq:(Medium) rs1240721262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18012869 Human_Splice_Rec_455718,Human_Splice_Rec_455746 RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_120923,RMVar_hsa_circ_22294,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813,RMVar_hsa_circ_338232,RMVar_hsa_circ_361281,RMVar_hsa_circ_349170,RMVar_hsa_circ_334076,RMVar_hsa_circ_319340,RMVar_hsa_circ_123656,RMVar_hsa_circ_4919,RMVar_hsa_circ_219815,RMVar_hsa_circ_219817,RMVar_hsa_circ_219819,RMVar_hsa_circ_219818,RMVar_hsa_circ_219816,RMVar_hsa_circ_320076,RMVar_hsa_circ_348802,RMVar_hsa_circ_32650,RMVar_hsa_circ_75350,RMVar_hsa_circ_107307,RMVar_hsa_circ_219821,RMVar_hsa_circ_219822 69499 RMVar_ID_69499 Human_SNP_ID_140985409 m1A Human chr3 + 81761504 81761504 81761504 CCTCGTAGTCCTCGGGCCGAGCCGCGGGAGTCATCGGAGCCGCCATATTCCGCCGCAGTCCAAGT CCTCGTAGTCCTCGGGCCGAGCCGCGGGAGTCGTCGGAGCCGCCATATTCCGCCGCAGTCCAAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:81761453..81761714 26863196 MeRIP-seq:(Medium) rs1359193851 Functional Loss SNV dbSNP153 33..33 33 - - - 69500 RMVar_ID_69500 Human_SNP_ID_140985410 m1A Human chr3 + 81761504 81761504 81761504 CCTCGTAGTCCTCGGGCCGAGCCGCGGGAGTCATCGGAGCCGCCATATTCCGCCGCAGTCCAAGT CCTCGTAGTCCTCGGGCCGAGCCGCGGGAGTCTTCGGAGCCGCCATATTCCGCCGCAGTCCAAGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:81761453..81761714 26863196 MeRIP-seq:(Medium) rs1359193851 Functional Loss SNV dbSNP153 33..33 33 - - - 69501 RMVar_ID_69501 Human_SNP_ID_140985464 m1A Human chr3 + 81761580 81761580 81761580 GAGAGGTCGAGTGGGGCCTGAGCGGGCGCTGGAGCTCTAGCTGGGACGCGGCGGCTAGGGCGGAG GAGAGGTCGAGTGGGGCCTGAGCGGGCGCTGGCGCTCTAGCTGGGACGCGGCGGCTAGGGCGGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:81761529..81761692 26863196 MeRIP-seq:(Medium) rs1164725104 Functional Loss SNV dbSNP153 33..33 33 - - - 69502 RMVar_ID_69502 Human_SNP_ID_142363924 m1A Human chr3 - 86978702 86978702 86978702 GGAGGATGAGGAGGAGGAGGAGGAGGAGAAAGACCAGCCTGCCGAGATGGAGTACCTTAACTCTC GGAGGATGAGGAGGAGGAGGAGGAGGAGAAAGTCCAGCCTGCCGAGATGGAGTACCTTAACTCTC T A VGLL3 Ensembl:ENSG00000206538 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:86978651..86978825 26863196 MeRIP-seq:(Medium) rs747861491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347012,RMVar_hsa_circ_219851 69503 RMVar_ID_69503 Human_SNP_ID_142363925 m1A Human chr3 - 86978702 86978702 86978702 GGAGGATGAGGAGGAGGAGGAGGAGGAGAAAGACCAGCCTGCCGAGATGGAGTACCTTAACTCTC GGAGGATGAGGAGGAGGAGGAGGAGGAGAAAGCCCAGCCTGCCGAGATGGAGTACCTTAACTCTC T G VGLL3 Ensembl:ENSG00000206538 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:86978651..86978825 26863196 MeRIP-seq:(Medium) rs747861491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347012,RMVar_hsa_circ_219851 69504 RMVar_ID_69504 Human_SNP_ID_142367032 m1A Human chr3 - 86990668 86990668 86990668 CGTCCCAGTATCTGCCCAACCCCATGGCAGCGACAACCTGCCCCACAGCCTACTATCAGCCGGCG CGTCCCAGTATCTGCCCAACCCCATGGCAGCGTCAACCTGCCCCACAGCCTACTATCAGCCGGCG T A VGLL3 Ensembl:ENSG00000206538 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:86990562..86990763 26863196 MeRIP-seq:(Medium) rs1162083544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_456133,Human_Splice_Rec_456139,Human_Splice_Rec_456145 69505 RMVar_ID_69505 Human_SNP_ID_142429178 m1A Human chr3 - 87227351 87227343 87227352 GCAGGACCCGCGGAAGGCTTGTATCCGCAGCTACCGCAGCCGCGTCACCCGGAGCTCAGGTGACC GCAGGACCCGCGGAAGGCTTGTATCCGCAGC_________CGCGTCACCCGGAGCTCAGGTGACC GGCTGCGGTA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:87227301..87227475;chr3:87227301..87227546;chr3:87227301..87227525 26863196 MeRIP-seq:(Medium) rs1334926802 Functional Loss DEL dbSNP153 32..40 33 - - - 69506 RMVar_ID_69506 Human_SNP_ID_142429183 m1A Human chr3 + 87227364 87227364 87227364 CCGGGTGACGCGGCTGCGGTAGCTGCGGATACAAGCCTTCCGCGGGTCCTGCCTGGCGACCCCGA CCGGGTGACGCGGCTGCGGTAGCTGCGGATACCAGCCTTCCGCGGGTCCTGCCTGGCGACCCCGA A C CHMP2B Ensembl:ENSG00000083937 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:87227301..87227525 26863196 MeRIP-seq:(Medium) rs574954693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608478,Human_RBP_ID_1314658,Human_RBP_ID_4754061,Human_RBP_ID_8579737,Human_RBP_ID_18011440,Human_RBP_ID_27059478 69507 RMVar_ID_69507 Human_SNP_ID_142429202 m1A Human chr3 + 87227425 87227425 87227425 CCGACCTCCTCCTGCTGTCTCTCCGCTCCGCCACCCCGAACCCGCCAAGGTCCTGTCCTTTTCCT CCGACCTCCTCCTGCTGTCTCTCCGCTCCGCCCCCCCGAACCCGCCAAGGTCCTGTCCTTTTCCT A C CHMP2B Ensembl:ENSG00000083937 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr3:87227324..87227575;chr3:87227301..87227500;chr3:87227301..87240333 26863196,26863410 MeRIP-seq:(Medium) rs1032371345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608479,Human_RBP_ID_18954534 69508 RMVar_ID_69508 Human_SNP_ID_142644862 m1A Human chr3 - 88052380 88052380 88052380 GTTTGACTTACCCCAGCTACCGTTAAATGAGGACAAATCACCTTAAAACATGTTCATTTGATTCA GTTTGACTTACCCCAGCTACCGTTAAATGAGGGCAAATCACCTTAAAACATGTTCATTTGATTCA T C CGGBP1 Ensembl:ENSG00000163320 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1051436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26823998 Human_miRNA_ID_1192391 GWAS_ID_8387,GWAS_ID_8388,GWAS_ID_8389,GWAS_ID_8390,GWAS_ID_8391,GWAS_ID_8392,GWAS_ID_8393 69509 RMVar_ID_69509 Human_SNP_ID_142646542 m1A Human chr3 + 88058904 88058901 88058904 AAAAGGAAGAAAGAGGAGCAAGGGAATAAGGGAGGAGGAGGATCCGTCGCTGCCGCCGTCGCCGC AAAAGGAAGAAAGAGGAGCAAGGGAATAAG___GGAGGAGGATCCGTCGCTGCCGCCGTCGCCGC GGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:88058784..88058975 26863196 MeRIP-seq:(Medium) rs1452713588 Functional Loss DEL dbSNP153 31..33 33 - - - 69510 RMVar_ID_69510 Human_SNP_ID_142646550 m1A Human chr3 - 88058930 88058913 88058931 CCGCCGCGGGGCTCGATCGGGCAACGGCGGCGACGGCGGCAGCGACGGATCCTCCTCCTCCCTTA CCGCCGCGGGGCTCGATCGGGCAACGGCGGC__________________TCCTCCTCCTCCCTTA ATCCGTCGCTGCCGCCGTC A CGGBP1 Ensembl:ENSG00000163320 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr3:88058827..88058959;chr3:88058826..88059000;chr3:88058801..88059000 26863196,26863410,26863410 MeRIP-seq:(Medium) rs777710809 Functional Loss DEL dbSNP153 32..49 33 - - - Human_RBP_ID_4754201,Human_RBP_ID_9333782 69511 RMVar_ID_69511 Human_SNP_ID_142646555 m1A Human chr3 - 88058922 88058922 88058922 GGGCTCGATCGGGCAACGGCGGCGACGGCGGCAGCGACGGATCCTCCTCCTCCCTTATTCCCTTG GGGCTCGATCGGGCAACGGCGGCGACGGCGGCGGCGACGGATCCTCCTCCTCCCTTATTCCCTTG T C CGGBP1 Ensembl:ENSG00000163320 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr3:88058872..88058962;chr3:88058876..88058950 26863196 MeRIP-seq:(Medium) rs1449103863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4754201,Human_RBP_ID_9333782 69512 RMVar_ID_69512 Human_SNP_ID_142646557 m1A Human chr3 - 88058930 88058922 88058931 CCGCCGCGGGGCTCGATCGGGCAACGGCGGCGACGGCGGCAGCGACGGATCCTCCTCCTCCCTTA CCGCCGCGGGGCTCGATCGGGCAACGGCGGC_________AGCGACGGATCCTCCTCCTCCCTTA TGCCGCCGTC T CGGBP1 Ensembl:ENSG00000163320 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr3:88058827..88058959;chr3:88058826..88059000;chr3:88058801..88059000 26863196,26863410,26863410 MeRIP-seq:(Medium) rs958493761 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_4754201,Human_RBP_ID_9333782 69513 RMVar_ID_69513 Human_SNP_ID_142646562 m1A Human chr3 - 88058930 88058928 88058930 CCGCCGCGGGGCTCGATCGGGCAACGGCGGCGACGGCGGCAGCGACGGATCCTCCTCCTCCCTTA CCGCCGCGGGGCTCGATCGGGCAACGGCGGCG__GGCGGCAGCGACGGATCCTCCTCCTCCCTTA CGT C CGGBP1 Ensembl:ENSG00000163320 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr3:88058827..88058959;chr3:88058826..88059000;chr3:88058801..88059000 26863196,26863410,26863410 MeRIP-seq:(Medium) rs749157639 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4754201,Human_RBP_ID_9333782 69514 RMVar_ID_69514 Human_SNP_ID_142646728 m1A Human chr3 + 88059287 88059286 88059287 AGCCTAGGCATCTACGGCGGCGGCGGCGGCGCAGGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC AGCCTAGGCATCTACGGCGGCGGCGGCGGCGC_GGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC CA C ZNF654 Ensembl:ENSG00000175105 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:88059240..88059436;chr3:88059239..88059481 26863196 MeRIP-seq:(Medium) rs1272979885 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18424020 69515 RMVar_ID_69515 Human_SNP_ID_142646730 m1A Human chr3 + 88059287 88059287 88059287 AGCCTAGGCATCTACGGCGGCGGCGGCGGCGCAGGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC AGCCTAGGCATCTACGGCGGCGGCGGCGGCGCCGGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC A C ZNF654 Ensembl:ENSG00000175105 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:88059240..88059436;chr3:88059239..88059481 26863196 MeRIP-seq:(Medium) rs577161373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424020 69516 RMVar_ID_69516 Human_SNP_ID_142646731 m1A Human chr3 + 88059287 88059287 88059287 AGCCTAGGCATCTACGGCGGCGGCGGCGGCGCAGGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC AGCCTAGGCATCTACGGCGGCGGCGGCGGCGCTGGGGCTGGTACGCGCTGGGCGGCGAGAGCCTC A T ZNF654 Ensembl:ENSG00000175105 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:88059240..88059436;chr3:88059239..88059481 26863196 MeRIP-seq:(Medium) rs577161373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424020 69517 RMVar_ID_69517 Human_SNP_ID_142646738 m1A Human chr3 - 88059293 88059293 88059293 CGCCATGAGGCTCTCGCCGCCCAGCGCGTACCAGCCCCTGCGCCGCCGCCGCCGCCGTAGATGCC CGCCATGAGGCTCTCGCCGCCCAGCGCGTACCTGCCCCTGCGCCGCCGCCGCCGCCGTAGATGCC T A CGGBP1 Ensembl:ENSG00000163320 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:88059235..88059474 26863196 MeRIP-seq:(Medium) rs1482738058 Functional Loss SNV dbSNP153 33..33 33 - - - 69518 RMVar_ID_69518 Human_SNP_ID_142662209 m1A Human chr3 - 88127382 88127382 88127382 CAGTGTCCTTTTTACCCCTTGGGTTCTTCATAACACTGTCACGTATACCTTAGCCCTATCCTCCT CAGTGTCCTTTTTACCCCTTGGGTTCTTCATAGCACTGTCACGTATACCTTAGCCCTATCCTCCT T C CGGBP1 Ensembl:ENSG00000163320 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:88127331..88127589 26863196 MeRIP-seq:(Medium) rs1346771288 Functional Loss SNV dbSNP153 33..33 33 - - - 69519 RMVar_ID_69519 Human_SNP_ID_237106777 m1A Human chr5 + 75336554 75336554 75336554 GGAGAGCAGAAGGAACGCACAGAAGACGCAGGAGAGGCACATTTCAGAGAGAATCCAGTATGCAA GGAGAGCAGAAGGAACGCACAGAAGACGCAGGCGAGGCACATTTCAGAGAGAATCCAGTATGCAA A C HMGCR Ensembl:ENSG00000113161 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:75336452..75336610 26863196 MeRIP-seq:(Medium) rs968060182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_663111 RMVar_hsa_circ_109552,RMVar_hsa_circ_232512 69520 RMVar_ID_69520 Human_SNP_ID_237150765 m1A Human chr5 - 75511579 75511579 75511579 GAAGATGGCGGCGGTAGCGGAGGTGTGAGTGGACGCGGGACTCAGCGGCCGGATTTTCTCTTCCC GAAGATGGCGGCGGTAGCGGAGGTGTGAGTGGGCGCGGGACTCAGCGGCCGGATTTTCTCTTCCC T C CERT1 Ensembl:ENSG00000113163 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:75511334..75511610;chr5:75511331..75511633 26863196 MeRIP-seq:(Medium) rs1046844894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788608,Human_RBP_ID_1322719,Human_RBP_ID_4839568,Human_RBP_ID_9306525,Human_RBP_ID_24116182,Human_RBP_ID_25933963 69521 RMVar_ID_69521 Human_SNP_ID_237150769 m1A Human chr5 + 75511588 75511588 75511588 AAATCCGGCCGCTGAGTCCCGCGTCCACTCACACCTCCGCTACCGCCGCCATCTTCCTGCCTGGC AAATCCGGCCGCTGAGTCCCGCGTCCACTCACCCCTCCGCTACCGCCGCCATCTTCCTGCCTGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:75511341..75511632 26863196 MeRIP-seq:(Medium) rs1322003439 Functional Loss SNV dbSNP153 33..33 33 - - - 69522 RMVar_ID_69522 Human_SNP_ID_237159084 m1A Human chr5 - 75547094 75547094 75547094 TTCTCTTTATCTAATCCTTCCATTCCTGCTTTATTATCATTAAGTCCCATCCTAAGCAGAAGATC TTCTCTTTATCTAATCCTTCCATTCCTGCTTTGTTATCATTAAGTCCCATCCTAAGCAGAAGATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:75547044..75547147;chr5:75547044..75547136 26863196 MeRIP-seq:(Medium) rs751040826 Functional Loss SNV dbSNP153 33..33 33 - - - 69523 RMVar_ID_69523 Human_SNP_ID_237370686 m1A Human chr5 - 76403342 76403342 76403342 GCCACGGCCGCCGCGCGCTGACACTGAAGTAAAAGTGAACTCTCCTCCCTCGCTCCCTGGCCGGT GCCACGGCCGCCGCGCGCTGACACTGAAGTAAGAGTGAACTCTCCTCCCTCGCTCCCTGGCCGGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr5:76403317..76403467;chr5:76403304..76403444 26863196 MeRIP-seq:(Medium) rs1160890146 Functional Loss SNV dbSNP153 33..33 33 - - - 69524 RMVar_ID_69524 Human_SNP_ID_237441714 m1A Human chr5 + 76707656 76707656 76707656 ACAAACATGTAAACCTATTTTCCTATGAAAAAAATTTTAAATGTCCCACTTGAATAACGTAATTC ACAAACATGTAAACCTATTTTCCTATGAAAAAGATTTTAAATGTCCCACTTGAATAACGTAATTC A G IQGAP2 Ensembl:ENSG00000145703 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1415557729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106691,RMVar_hsa_circ_232587 69525 RMVar_ID_69525 Human_SNP_ID_237530177 m1A Human chr5 + 77059676 77059676 77059676 TGAAGAATCCAAAATATAAAGATAGAGCTGGAAAACGTAGGGAGCAGGTTGGAAGTGAAGGAACT TGAAGAATCCAAAATATAAAGATAGAGCTGGACAACGTAGGGAGCAGGTTGGAAGTGAAGGAACT A C AC008581.2,AGGF1 Ensembl:ENSG00000285000,Ensembl:ENSG00000164252 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:77059593..77059737 26863196 MeRIP-seq:(Medium) rs1474310926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1999717,Human_RBP_ID_8892355,Human_RBP_ID_27825532 Human_Splice_Rec_665168,Human_Splice_Rec_665169,Human_Splice_Rec_665206,Human_Splice_Rec_665207 RMVar_hsa_circ_58852,RMVar_hsa_circ_57694,RMVar_hsa_circ_49082,RMVar_hsa_circ_58599,RMVar_hsa_circ_307619,RMVar_hsa_circ_323479 69526 RMVar_ID_69526 Human_SNP_ID_237533311 m1A Human chr5 + 77074202 77074201 77074203 GGGGGCAGAGGGGGACTTGAATGTCAGGTGACAGAGTCAAAGCTTGCACTCAAGTAGGTGATTGA GGGGGCAGAGGGGGACTTGAATGTCAGGTGAC__AGTCAAAGCTTGCACTCAAGTAGGTGATTGA CAG C AC008581.2,AC008581.1 Ensembl:ENSG00000285000,Ensembl:ENSG00000250615 Protein coding,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:77074201..77074225 26863196 MeRIP-seq:(Medium) rs886261686 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_665223 69527 RMVar_ID_69527 Human_SNP_ID_237534477 m1A Human chr5 - 77077397 77077381 77077397 GGAGCGGCGCGAGCTGGCCGTGGAGCAGGGCGAGCGCGCCCTGGAGCGGAGGCGGAGGGCGCTGC GGAGCGGCGCGAGCTGGCCGTGGAGCAGGGCG________________GAGGCGGAGGGCGCTGC CCGCTCCAGGGCGCGCT C ZBED3 Ensembl:ENSG00000132846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:77077095..77079048 26863196 MeRIP-seq:(Medium) rs1224152945 Functional Loss DEL dbSNP153 33..48 33 - - - 69528 RMVar_ID_69528 Human_SNP_ID_237534610 m1A Human chr5 - 77077658 77077658 77077658 GGGCCACTGGGCCACCTGCCGTCTGTGCGGGGAGCAGGTGGGCCGCGGCCCGGGCTTCCACGCGG GGGCCACTGGGCCACCTGCCGTCTGTGCGGGGTGCAGGTGGGCCGCGGCCCGGGCTTCCACGCGG T A ZBED3 Ensembl:ENSG00000132846 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:77077607..77077715 32194978 MeRIP-seq:(Medium) rs1345944526 Functional Loss SNV dbSNP153 33..33 33 - - - 69529 RMVar_ID_69529 Human_SNP_ID_237534611 m1A Human chr5 - 77077658 77077658 77077658 GGGCCACTGGGCCACCTGCCGTCTGTGCGGGGAGCAGGTGGGCCGCGGCCCGGGCTTCCACGCGG GGGCCACTGGGCCACCTGCCGTCTGTGCGGGGCGCAGGTGGGCCGCGGCCCGGGCTTCCACGCGG T G ZBED3 Ensembl:ENSG00000132846 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:77077607..77077715 32194978 MeRIP-seq:(Medium) rs1345944526 Functional Loss SNV dbSNP153 33..33 33 - - - 69530 RMVar_ID_69530 Human_SNP_ID_237535276 m1A Human chr5 + 77080521 77080521 77080521 GCCTGGGCAGCCCTTCGATTTTGGAGGTCTTAACCGGTGGAAGGCAGCACGGGGCAAAACTGCCT GCCTGGGCAGCCCTTCGATTTTGGAGGTCTTACCCGGTGGAAGGCAGCACGGGGCAAAACTGCCT A C AC008581.2 Ensembl:ENSG00000285000 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:77080426..77080575 26863196 MeRIP-seq:(Medium) rs1382871754 Functional Loss SNV dbSNP153 33..33 33 - - - 69531 RMVar_ID_69531 Human_SNP_ID_237535281 m1A Human chr5 - 77080526 77080526 77080526 AGGTGAGGCAGTTTTGCCCCGTGCTGCCTTCCACCGGTTAAGACCTCCAAAATCGAAGGGCTGCC AGGTGAGGCAGTTTTGCCCCGTGCTGCCTTCCGCCGGTTAAGACCTCCAAAATCGAAGGGCTGCC T C SNORA47,ZBED3 Ensembl:ENSG00000238961,Ensembl:ENSG00000132846 snoRNA,Protein coding exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:77080426..77080575 26863196 MeRIP-seq:(Medium) rs1162896006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_164153,Human_RBP_ID_840241,Human_RBP_ID_1064118,Human_RBP_ID_5302301,Human_RBP_ID_8269628,Human_RBP_ID_8894531,Human_RBP_ID_9437272,Human_RBP_ID_15516164,Human_RBP_ID_17090688,Human_RBP_ID_17671774,Human_RBP_ID_19128531,Human_RBP_ID_22746170,Human_RBP_ID_24548310,Human_RBP_ID_26575916 69532 RMVar_ID_69532 Human_SNP_ID_237536771 m1A Human chr5 + 77087162 77087161 77087163 GGCCGGAGCCGGCGGCGGGTCGGGAGTCCGAGATGGTAGATCCCCCTCCAGGCGCCTCGCTGACA GGCCGGAGCCGGCGGCGGGTCGGGAGTCCGAG__GGTAGATCCCCCTCCAGGCGCCTCGCTGACA GAT G AC008581.2,ZBED3-AS1,AC022414.1 Ensembl:ENSG00000285000,Ensembl:ENSG00000250802,Ensembl:ENSG00000284762 Protein coding,lincRNA,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:77087057..77087244;chr5:77086889..77087298;chr5:77087092..77087246 26863196 MeRIP-seq:(Medium) rs1158109965 Functional Loss DEL dbSNP153 33..34 33 - - - 69533 RMVar_ID_69533 Human_SNP_ID_237559596 m1A Human chr5 + 77189409 77189409 77189409 AGGATGCAAGTGTCAGATGTGGTGAGCACCAGAAAGAAAGATAAAGCAGGAAAGAGCAATAATAA AGGATGCAAGTGTCAGATGTGGTGAGCACCAGGAAGAAAGATAAAGCAGGAAAGAGCAATAATAA A G AC022414.1 Ensembl:ENSG00000284762 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:77189391..77189479 26863196 MeRIP-seq:(Medium) rs1361975008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24116625 69534 RMVar_ID_69534 Human_SNP_ID_237559662 m1A Human chr5 + 77189625 77189625 77189625 GGGAGGGATAGTGGGTGCAAAGGCCCTGAAGGAGCATGTCGGCATGCCCATGGTGCAGCAAGGAG GGGAGGGATAGTGGGTGCAAAGGCCCTGAAGGTGCATGTCGGCATGCCCATGGTGCAGCAAGGAG A T AC022414.1 Ensembl:ENSG00000284762 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:77189613..77189858 26863196 MeRIP-seq:(Medium) rs910343793 Functional Loss SNV dbSNP153 33..33 33 - - - 69535 RMVar_ID_69535 Human_SNP_ID_237559673 m1A Human chr5 + 77189642 77189642 77189642 CAAAGGCCCTGAAGGAGCATGTCGGCATGCCCATGGTGCAGCAAGGAGGCTGCTGGAGCAGGAGG CAAAGGCCCTGAAGGAGCATGTCGGCATGCCCGTGGTGCAGCAAGGAGGCTGCTGGAGCAGGAGG A G AC022414.1 Ensembl:ENSG00000284762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:77189629..77189871 26863196 MeRIP-seq:(Medium) rs575181219 Functional Loss SNV dbSNP153 33..33 33 - - - 69536 RMVar_ID_69536 Human_SNP_ID_237563141 m1A Human chr5 + 77206409 77206409 77206409 GGCTAAGGGGAATCAGGAGTGGTAGAGGAACAATAGAGCTATGTGGGTTGCAATTTCAAACACGG GGCTAAGGGGAATCAGGAGTGGTAGAGGAACATTAGAGCTATGTGGGTTGCAATTTCAAACACGG A T AC022414.1 Ensembl:ENSG00000284762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:77206391..77206674 26863196 MeRIP-seq:(Medium) rs992754030 Functional Loss SNV dbSNP153 33..33 33 - - - 69537 RMVar_ID_69537 Human_SNP_ID_237563941 m1A Human chr5 + 77210320 77210320 77210320 GCCAGCTGCCGCGCACAGGGGCCCCGCGGCGGAGCCGAGCCGCGGGCACGCTCTGCCCTGTCGGG GCCAGCTGCCGCGCACAGGGGCCCCGCGGCGGGGCCGAGCCGCGGGCACGCTCTGCCCTGTCGGG A G AC022414.1 Ensembl:ENSG00000284762 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:77210309..77210618 26863196 MeRIP-seq:(Medium) rs1266661150 Functional Loss SNV dbSNP153 33..33 33 - - - 69538 RMVar_ID_69538 Human_SNP_ID_237563987 m1A Human chr5 - 77210497 77210497 77210497 CAGGGCGCCCGCCCGCCTGCCCGCCTGCCTGCACCTTCTTTCCCCACTTTCGGTCTGCGCCCGTC CAGGGCGCCCGCCCGCCTGCCCGCCTGCCTGCCCCTTCTTTCCCCACTTTCGGTCTGCGCCCGTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:77210448..77213963 26863196 MeRIP-seq:(Medium) rs1222357858 Functional Loss SNV dbSNP153 33..33 33 - - - 69539 RMVar_ID_69539 Human_SNP_ID_237563990 m1A Human chr5 + 77210504 77210504 77210504 GCAGACCGAAAGTGGGGAAAGAAGGTGCAGGCAGGCGGGCAGGCGGGCGGGCGCCCTGGCCCAGG GCAGACCGAAAGTGGGGAAAGAAGGTGCAGGCCGGCGGGCAGGCGGGCGGGCGCCCTGGCCCAGG A C AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:77210405..77210718 26863196 MeRIP-seq:(Medium) rs1347770956 Functional Loss SNV dbSNP153 33..33 33 - - - 69540 RMVar_ID_69540 Human_SNP_ID_237563991 m1A Human chr5 + 77210504 77210504 77210504 GCAGACCGAAAGTGGGGAAAGAAGGTGCAGGCAGGCGGGCAGGCGGGCGGGCGCCCTGGCCCAGG GCAGACCGAAAGTGGGGAAAGAAGGTGCAGGCGGGCGGGCAGGCGGGCGGGCGCCCTGGCCCAGG A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:77210405..77210718 26863196 MeRIP-seq:(Medium) rs1347770956 Functional Loss SNV dbSNP153 33..33 33 - - - 69541 RMVar_ID_69541 Human_SNP_ID_237564035 m1A Human chr5 + 77210648 77210648 77210648 GCGGGGAGCGTGTTTGGGGCGCCGCGGCGGGGAGGGTGGCGGCCGCTGGTGCGCGCGGGGCGCTG GCGGGGAGCGTGTTTGGGGCGCCGCGGCGGGGGGGGTGGCGGCCGCTGGTGCGCGCGGGGCGCTG A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:77210520..77210771 26863196 MeRIP-seq:(Medium) rs1484977569 Functional Loss SNV dbSNP153 33..33 33 - - - 69542 RMVar_ID_69542 Human_SNP_ID_237568213 m1A Human chr5 - 77228970 77228970 77228970 GCCAAAACCTGGACATCATTCCAGACCGTTCTATCTCCCACATCTGCCTTGCCCAAATATCAAAT GCCAAAACCTGGACATCATTCCAGACCGTTCTCTCTCCCACATCTGCCTTGCCCAAATATCAAAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:77228963..77229032 26863196 MeRIP-seq:(Medium) rs1326668709 Functional Loss SNV dbSNP153 33..33 33 - - - 69543 RMVar_ID_69543 Human_SNP_ID_237585800 m1A Human chr5 + 77308324 77308324 77308324 GCAAAGTGTGGGTCAGGACTAGAGGAGCTGGTAAACTGAGGCACCCACGCCGGTAGTGCAGGTAG GCAAAGTGTGGGTCAGGACTAGAGGAGCTGGTGAACTGAGGCACCCACGCCGGTAGTGCAGGTAG A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:77308322..77308426 26863196 MeRIP-seq:(Medium) rs970114 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8394,GWAS_ID_8395,GWAS_ID_8396,GWAS_ID_8397,GWAS_ID_8398,GWAS_ID_8399,GWAS_ID_8400,GWAS_ID_8401,GWAS_ID_8402,GWAS_ID_8403,GWAS_ID_8404,GWAS_ID_8405,GWAS_ID_8406,GWAS_ID_8407,GWAS_ID_8408,GWAS_ID_8409,GWAS_ID_8410,GWAS_ID_8411,GWAS_ID_8412,GWAS_ID_8413 69544 RMVar_ID_69544 Human_SNP_ID_237594604 m1A Human chr5 + 77347731 77347731 77347731 GTGGCAGCTCTTGGGAGTGGACTAGGTAGGGGAATCAGGGAAGGCTTCCTGGAAGAGAAGAGGGA GTGGCAGCTCTTGGGAGTGGACTAGGTAGGGGGATCAGGGAAGGCTTCCTGGAAGAGAAGAGGGA A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:77347726..77347888 26863196 MeRIP-seq:(Medium) rs1261007096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363892,RMVar_hsa_circ_24039,RMVar_hsa_circ_25848,RMVar_hsa_circ_363286,RMVar_hsa_circ_3338,RMVar_hsa_circ_48389 69545 RMVar_ID_69545 Human_SNP_ID_237608887 m1A Human chr5 + 77407678 77407678 77407678 TTCTGTGAGAGAAAATTAGAGTAGGGCCCTTAAGTAGGTTGGAAGAGAGGGTGGTCAGGGAAACT TTCTGTGAGAGAAAATTAGAGTAGGGCCCTTAGGTAGGTTGGAAGAGAGGGTGGTCAGGGAAACT A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:77407671..77407800 26863196 MeRIP-seq:(Medium) rs551824326 Functional Loss SNV dbSNP153 33..33 33 - - - 69546 RMVar_ID_69546 Human_SNP_ID_237630859 m1A Human chr5 - 77489570 77489570 77489570 TTTTTGCTTTTTTTTTTTTTTCAATACAAGAAATCTCCTTTACAGACAATAGGTGAAGAACAAAC TTTTTGCTTTTTTTTTTTTTTCAATACAAGAAGTCTCCTTTACAGACAATAGGTGAAGAACAAAC T C WDR41 Ensembl:ENSG00000164253 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:77489520..77491240 26863196 MeRIP-seq:(Medium) rs1351672391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_665822,Human_Splice_Rec_665858,Human_Splice_Rec_665906,Human_Splice_Rec_665916,Human_Splice_Rec_665934,Human_Splice_Rec_665935,Human_Splice_Rec_665940,Human_Splice_Rec_665954,Human_Splice_Rec_665966,Human_Splice_Rec_665980,Human_Splice_Rec_665992,Human_Splice_Rec_666004,Human_Splice_Rec_666016,Human_Splice_Rec_666028,Human_Splice_Rec_666052,Human_Splice_Rec_666062,Human_Splice_Rec_666072,Human_Splice_Rec_666084,Human_Splice_Rec_666106,Human_Splice_Rec_666112 Human_miRNA_ID_2620306 RMVar_hsa_circ_359418,RMVar_hsa_circ_271244,RMVar_hsa_circ_124890,RMVar_hsa_circ_232624,RMVar_hsa_circ_350175,RMVar_hsa_circ_232623,RMVar_hsa_circ_62979,RMVar_hsa_circ_355404,RMVar_hsa_circ_232629,RMVar_hsa_circ_327896,RMVar_hsa_circ_232633,RMVar_hsa_circ_232634,RMVar_hsa_circ_345934 69547 RMVar_ID_69547 Human_SNP_ID_237630862 m1A Human chr5 - 77489574 77489574 77489574 TTGTTTTTTGCTTTTTTTTTTTTTTCAATACAAGAAATCTCCTTTACAGACAATAGGTGAAGAAC TTGTTTTTTGCTTTTTTTTTTTTTTCAATACAGGAAATCTCCTTTACAGACAATAGGTGAAGAAC T C WDR41 Ensembl:ENSG00000164253 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:77489526..77489624 26863196 MeRIP-seq:(Medium) rs201202661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7471178 Human_Splice_Rec_665935 RMVar_hsa_circ_124890,RMVar_hsa_circ_232623 69548 RMVar_ID_69548 Human_SNP_ID_237631709 m1A Human chr5 - 77492475 77492475 77492475 ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCAGCCGCCCCCGCCGTCGGCCGCCGCACCCCAAG ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCGGCCGCCCCCGCCGTCGGCCGCCGCACCCCAAG T C WDR41 Ensembl:ENSG00000164253 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:77492376..77492500 26863410 MeRIP-seq:(Medium) rs903631323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4840217 Human_miRNA_ID_2146196,Human_miRNA_ID_2386478,Human_miRNA_ID_2387951,Human_miRNA_ID_2399105,Human_miRNA_ID_2987628,Human_miRNA_ID_3021319,Human_miRNA_ID_3030157 RMVar_hsa_circ_124890,RMVar_hsa_circ_232623 69549 RMVar_ID_69549 Human_SNP_ID_237631710 m1A Human chr5 - 77492475 77492475 77492475 ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCAGCCGCCCCCGCCGTCGGCCGCCGCACCCCAAG ACTCGGAGCAGCGCGCGCCCCGCAATCGCCGCCGCCGCCCCCGCCGTCGGCCGCCGCACCCCAAG T G WDR41 Ensembl:ENSG00000164253 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:77492376..77492500 26863410 MeRIP-seq:(Medium) rs903631323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4840217 Human_miRNA_ID_2146196,Human_miRNA_ID_2386478,Human_miRNA_ID_2387951,Human_miRNA_ID_2399105,Human_miRNA_ID_2987628,Human_miRNA_ID_3021319,Human_miRNA_ID_3030157 RMVar_hsa_circ_124890,RMVar_hsa_circ_232623 69550 RMVar_ID_69550 Human_SNP_ID_237679327 m1A Human chr5 - 77693354 77693352 77693355 ATCTTTGAACGTCTCACAGAGATTCTCATTCTAGGCAGAGATCCTACAAGAATCCAGGATGATGA ATCTTTGAACGTCTCACAGAGATTCTCATTC___GCAGAGATCCTACAAGAATCCAGGATGATGA CCTA C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:77693332..77693410 26863196 MeRIP-seq:(Medium) rs1261919447 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_646800,Human_RBP_ID_17708561 Human_Splice_Rec_666127,Human_Splice_Rec_666131,Human_Splice_Rec_666137,Human_Splice_Rec_666149,Human_Splice_Rec_666154,Human_Splice_Rec_666161,Human_Splice_Rec_666167 RMVar_hsa_circ_360359 69551 RMVar_ID_69551 Human_SNP_ID_237682773 m1A Human chr5 + 77708327 77708327 77708327 TTTCTTCTTGTTGTTTTGCCTCTTTTTCATACATCACTTTTTCTTTGACCAACCTATAAAAAAGC TTTCTTCTTGTTGTTTTGCCTCTTTTTCATACGTCACTTTTTCTTTGACCAACCTATAAAAAAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:77708276..77708350 26863196 MeRIP-seq:(Medium) rs1331246233 Functional Loss SNV dbSNP153 33..33 33 - - - 69552 RMVar_ID_69552 Human_SNP_ID_237682775 m1A Human chr5 - 77708340 77708340 77708340 TAAAACATTTTTGGCTTTTTTATAGGTTGGTCAAAGAAAAAGTGATGTATGAAAAAGAGGCAAAA TAAAACATTTTTGGCTTTTTTATAGGTTGGTCCAAGAAAAAGTGATGTATGAAAAAGAGGCAAAA T G TBCA Ensembl:ENSG00000171530 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:77708226..77708401 26863196 MeRIP-seq:(Medium) rs1267987420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1660425,Human_RBP_ID_4840234,Human_RBP_ID_9397970,Human_RBP_ID_17662875,Human_RBP_ID_24116855,Human_RBP_ID_24548112,Human_RBP_ID_26350994,Human_RBP_ID_27826515 Human_Splice_Rec_666124,Human_Splice_Rec_666125,Human_Splice_Rec_666129,Human_Splice_Rec_666134,Human_Splice_Rec_666135,Human_Splice_Rec_666140,Human_Splice_Rec_666141,Human_Splice_Rec_666144,Human_Splice_Rec_666145,Human_Splice_Rec_666152,Human_Splice_Rec_666153,Human_Splice_Rec_666156,Human_Splice_Rec_666157,Human_Splice_Rec_666164,Human_Splice_Rec_666165 Human_miRNA_ID_1700076,Human_miRNA_ID_2710825,Human_miRNA_ID_2871071 RMVar_hsa_circ_21844,RMVar_hsa_circ_360359,RMVar_hsa_circ_232635,RMVar_hsa_circ_357199 69553 RMVar_ID_69553 Human_SNP_ID_237779028 m1A Human chr5 - 78110287 78110287 78110287 CTAAAACTTCAGATTCTTCAAATGACGAATCTAGTTCAATAGAAGACAGTTCTTCCGATTCTGAA CTAAAACTTCAGATTCTTCAAATGACGAATCTTGTTCAATAGAAGACAGTTCTTCCGATTCTGAA T A AP3B1 Ensembl:ENSG00000132842 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:78110226..78110350 32194978 MeRIP-seq:(Medium) rs181965631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18847404 Human_Splice_Rec_666210,Human_Splice_Rec_666211,Human_Splice_Rec_666262,Human_Splice_Rec_666263,Human_Splice_Rec_666294,Human_Splice_Rec_666295,Human_Splice_Rec_666304,Human_Splice_Rec_666305 RMVar_hsa_circ_6209,RMVar_hsa_circ_101916,RMVar_hsa_circ_113230,RMVar_hsa_circ_115151,RMVar_hsa_circ_105659,RMVar_hsa_circ_232638,RMVar_hsa_circ_85016,RMVar_hsa_circ_232640,RMVar_hsa_circ_232641,RMVar_hsa_circ_232639,RMVar_hsa_circ_232637,RMVar_hsa_circ_50562,RMVar_hsa_circ_310459,RMVar_hsa_circ_332194,RMVar_hsa_circ_357103,RMVar_hsa_circ_366536,RMVar_hsa_circ_370007,RMVar_hsa_circ_355667,RMVar_hsa_circ_311049,RMVar_hsa_circ_295881,RMVar_hsa_circ_307409,RMVar_hsa_circ_290833,RMVar_hsa_circ_76410,RMVar_hsa_circ_112984,RMVar_hsa_circ_274772,RMVar_hsa_circ_102741,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_36563,RMVar_hsa_circ_232648,RMVar_hsa_circ_232652,RMVar_hsa_circ_232654,RMVar_hsa_circ_232656,RMVar_hsa_circ_232658,RMVar_hsa_circ_232657,RMVar_hsa_circ_232655,RMVar_hsa_circ_232653,RMVar_hsa_circ_232650,RMVar_hsa_circ_232651,RMVar_hsa_circ_232649,RMVar_hsa_circ_232660,RMVar_hsa_circ_100287,RMVar_hsa_circ_356771,RMVar_hsa_circ_232647,RMVar_hsa_circ_360253,RMVar_hsa_circ_333887,RMVar_hsa_circ_232661,RMVar_hsa_circ_289887,RMVar_hsa_circ_358441,RMVar_hsa_circ_360737,RMVar_hsa_circ_361542,RMVar_hsa_circ_355639,RMVar_hsa_circ_232663,RMVar_hsa_circ_62264,RMVar_hsa_circ_232662 69554 RMVar_ID_69554 Human_SNP_ID_237805859 m1A Human chr5 - 78220969 78220969 78220969 TCATGGCTCACTGCAGCCTCGACCTCCCCAGCACAAGCAATCCTCCTGTCCCAGCCTCCTGAGTA TCATGGCTCACTGCAGCCTCGACCTCCCCAGCGCAAGCAATCCTCCTGTCCCAGCCTCCTGAGTA T C AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:78220857..78220984 26863196 MeRIP-seq:(Medium) rs1393130725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6209,RMVar_hsa_circ_113230,RMVar_hsa_circ_232637,RMVar_hsa_circ_370007,RMVar_hsa_circ_76410,RMVar_hsa_circ_112984,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_30412,RMVar_hsa_circ_232648,RMVar_hsa_circ_232649,RMVar_hsa_circ_232647,RMVar_hsa_circ_266087,RMVar_hsa_circ_266769,RMVar_hsa_circ_88465,RMVar_hsa_circ_124182,RMVar_hsa_circ_269167,RMVar_hsa_circ_232668,RMVar_hsa_circ_232669,RMVar_hsa_circ_232671,RMVar_hsa_circ_105490,RMVar_hsa_circ_301214,RMVar_hsa_circ_50605,RMVar_hsa_circ_328169,RMVar_hsa_circ_107294,RMVar_hsa_circ_232672,RMVar_hsa_circ_232673 69555 RMVar_ID_69555 Human_SNP_ID_237819135 m1A Human chr5 - 78278639 78278634 78278640 AACCACTGTGTAATAGTTCCTCATAATTAATTAGTCCCCCCCCCCCTTTTTTTTTTTTTTTTTTT AACCACTGTGTAATAGTTCCTCATAATTAAT______CCCCCCCCCTTTTTTTTTTTTTTTTTTT GGGACTA G AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:78278542..78278716 26863196 MeRIP-seq:(Medium) rs1404098498 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_112984,RMVar_hsa_circ_232647 69556 RMVar_ID_69556 Human_SNP_ID_237839465 m1A Human chr5 + 78360332 78360332 78360332 CGCAGCTGGCCTCCGGCTGAGAGCGGAGGGGAAGGGTTCCATACTCTCCGAGGATCCCGCGGGCT CGCAGCTGGCCTCCGGCTGAGAGCGGAGGGGAGGGGTTCCATACTCTCCGAGGATCCCGCGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:78360284..78360369 26863196 MeRIP-seq:(Medium) rs939861919 Functional Loss SNV dbSNP153 33..33 33 - - - 69557 RMVar_ID_69557 Human_SNP_ID_237839650 m1A Human chr5 + 78360654 78360654 78360654 GTCTCTCTCTCTGCGCCTGGGTCGGGTGGGTGACGCCGAGAGCCAGAGAGATGTCGGATTTCGAC GTCTCTCTCTCTGCGCCTGGGTCGGGTGGGTGGCGCCGAGAGCCAGAGAGATGTCGGATTTCGAC A G SCAMP1 Ensembl:ENSG00000085365 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:78360554..78360696 26863196 MeRIP-seq:(Medium) rs531619824 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_838683,Human_RBP_ID_946631,Human_RBP_ID_4840383,Human_RBP_ID_18425127 Human_Splice_Rec_666323,Human_Splice_Rec_666337,Human_Splice_Rec_666351,Human_Splice_Rec_666367 Human_miRNA_ID_2017673,Human_miRNA_ID_2082743 RMVar_hsa_circ_113898,RMVar_hsa_circ_232677 69558 RMVar_ID_69558 Human_SNP_ID_237839651 m1A Human chr5 + 78360654 78360654 78360654 GTCTCTCTCTCTGCGCCTGGGTCGGGTGGGTGACGCCGAGAGCCAGAGAGATGTCGGATTTCGAC GTCTCTCTCTCTGCGCCTGGGTCGGGTGGGTGTCGCCGAGAGCCAGAGAGATGTCGGATTTCGAC A T SCAMP1 Ensembl:ENSG00000085365 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:78360554..78360696 26863196 MeRIP-seq:(Medium) rs531619824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838683,Human_RBP_ID_946631,Human_RBP_ID_4840383,Human_RBP_ID_18425127 Human_Splice_Rec_666323,Human_Splice_Rec_666337,Human_Splice_Rec_666351,Human_Splice_Rec_666367 Human_miRNA_ID_2017673,Human_miRNA_ID_2082743 RMVar_hsa_circ_113898,RMVar_hsa_circ_232677 69559 RMVar_ID_69559 Human_SNP_ID_237846506 m1A Human chr5 + 78388745 78388745 78388745 TTATTTTCCTCTGTTAGCCTTGCTGCATGACCACAAGTATAGATAAAGCAAATGGTATGTAAATA TTATTTTCCTCTGTTAGCCTTGCTGCATGACCGCAAGTATAGATAAAGCAAATGGTATGTAAATA A G SCAMP1 Ensembl:ENSG00000085365 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:78388739..78388925 26863196 MeRIP-seq:(Medium) rs936006214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8622434 RMVar_hsa_circ_56136,RMVar_hsa_circ_113898,RMVar_hsa_circ_232677 69560 RMVar_ID_69560 Human_SNP_ID_237846510 m1A Human chr5 + 78388763 78388763 78388763 CTTGCTGCATGACCACAAGTATAGATAAAGCAAATGGTATGTAAATATCAAAATTATTTTTTAAA CTTGCTGCATGACCACAAGTATAGATAAAGCAGATGGTATGTAAATATCAAAATTATTTTTTAAA A G SCAMP1 Ensembl:ENSG00000085365 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:78388761..78388925 26863410 MeRIP-seq:(Medium) rs865926310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8622434 RMVar_hsa_circ_56136,RMVar_hsa_circ_113898,RMVar_hsa_circ_232677 69561 RMVar_ID_69561 Human_SNP_ID_237853153 m1A Human chr5 + 78415417 78415417 78415417 CACTTGACTATGAGAGAGCAGGGAATGAAGAGATGCAGATTTTGGGATTTTTCATTTTATTGGTG CACTTGACTATGAGAGAGCAGGGAATGAAGAGGTGCAGATTTTGGGATTTTTCATTTTATTGGTG A G SCAMP1 Ensembl:ENSG00000085365 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:78415413..78415575 26863196 MeRIP-seq:(Medium) rs1042578316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113898,RMVar_hsa_circ_232677,RMVar_hsa_circ_282195,RMVar_hsa_circ_285446,RMVar_hsa_circ_365953,RMVar_hsa_circ_232678 69562 RMVar_ID_69562 Human_SNP_ID_237889864 m1A Human chr5 - 78558987 78558987 78558987 ATGGAGGCAGGTACCCAGGGAGTTAGCTTTGGACAGGAACAGGGCAGCTCTCTGTGGCACAGGAG ATGGAGGCAGGTACCCAGGGAGTTAGCTTTGGGCAGGAACAGGGCAGCTCTCTGTGGCACAGGAG T C LHFPL2 Ensembl:ENSG00000145685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:78558981..78559088 26863196 MeRIP-seq:(Medium) rs370321239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9180724 RMVar_hsa_circ_232684,RMVar_hsa_circ_340205,RMVar_hsa_circ_370596,RMVar_hsa_circ_232683 69563 RMVar_ID_69563 Human_SNP_ID_237903638 m1A Human chr5 + 78615970 78615970 78615970 GCAAAGCTGGTGCTAGGTAGGTTCTCAGGACCAGGAATGCTTACCTAACAGTTGCACTCTCTTCT GCAAAGCTGGTGCTAGGTAGGTTCTCAGGACCCGGAATGCTTACCTAACAGTTGCACTCTCTTCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:78615967..78616096 26863196 MeRIP-seq:(Medium) rs1162144865 Functional Loss SNV dbSNP153 33..33 33 - - - 69564 RMVar_ID_69564 Human_SNP_ID_237939447 m1A Human chr5 + 78762034 78762034 78762034 TGCACGTGGCTGGTAGTACAATCTCTAGAACAAGAACAGGGCCTCTGACCTCCAGGCCACATGTT TGCACGTGGCTGGTAGTACAATCTCTAGAACACGAACAGGGCCTCTGACCTCCAGGCCACATGTT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:78761940..78762067 26863196 MeRIP-seq:(Medium) rs1223190603 Functional Loss SNV dbSNP153 33..33 33 - - - 69565 RMVar_ID_69565 Human_SNP_ID_237993601 m1A Human chr5 - 78984859 78984859 78984859 GCCGGCGCCCTGCCGCTCCTACCCGGCCCTTGAGGCCGCGGGCGCTGGCAGGCGGGGCTCGGACC GCCGGCGCCCTGCCGCTCCTACCCGGCCCTTGGGGCCGCGGGCGCTGGCAGGCGGGGCTCGGACC T C ARSB Ensembl:ENSG00000113273 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:78984809..78984885 26863196 MeRIP-seq:(Medium) rs1239543905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19125869 RMVar_hsa_circ_318434,RMVar_hsa_circ_103538,RMVar_hsa_circ_352496,RMVar_hsa_circ_232691,RMVar_hsa_circ_232694,RMVar_hsa_circ_345495,RMVar_hsa_circ_352393,RMVar_hsa_circ_232696,RMVar_hsa_circ_69054 69566 RMVar_ID_69566 Human_SNP_ID_238057028 m1A Human chr5 + 79236176 79236176 79236176 CATTGTGGCGATGCTGAGGCGCAGAGTTTAGGAGACGGGTTCATCAGTCAGGCCGGCTCCGGGCT CATTGTGGCGATGCTGAGGCGCAGAGTTTAGGGGACGGGTTCATCAGTCAGGCCGGCTCCGGGCT A G JMY Ensembl:ENSG00000152409 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:79236126..79236945 26863196 MeRIP-seq:(Medium) rs1224274708 Functional Loss SNV dbSNP153 33..33 33 - - - 69567 RMVar_ID_69567 Human_SNP_ID_238057043 m1A Human chr5 + 79236193 79236193 79236193 GGCGCAGAGTTTAGGAGACGGGTTCATCAGTCAGGCCGGCTCCGGGCTTTCTGCAGCAGCACCAG GGCGCAGAGTTTAGGAGACGGGTTCATCAGTCTGGCCGGCTCCGGGCTTTCTGCAGCAGCACCAG A T JMY Ensembl:ENSG00000152409 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79236146..79236956 26863196 MeRIP-seq:(Medium) rs1035625865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4840636,Human_RBP_ID_15522399 Human_miRNA_ID_1198930 69568 RMVar_ID_69568 Human_SNP_ID_238057454 m1A Human chr5 + 79237118 79237118 79237118 GCCAAACCCATCCCGGGTCAGAAAACATCTGAAGCCGACGATGCGGCGGGGGCAGCCGCTGCAGC GCCAAACCCATCCCGGGTCAGAAAACATCTGAGGCCGACGATGCGGCGGGGGCAGCCGCTGCAGC A G JMY Ensembl:ENSG00000152409 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79237069..79237338 26863196 MeRIP-seq:(Medium) rs1044484469 Functional Loss SNV dbSNP153 33..33 33 - - - 69569 RMVar_ID_69569 Human_SNP_ID_238106469 m1A Human chr5 - 79427801 79427788 79427801 GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAAAGGAAGGAAGGAAGGAAATGAAGGAAAGGAAGG GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAA_____________GGAAATGAAGGAAAGGAAGG CTTCCTTCCTTCCT C HOMER1 Ensembl:ENSG00000152413 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:79427750..79427838 26863196 MeRIP-seq:(Medium) rs1172894461 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_17069733 RMVar_hsa_circ_2953,RMVar_hsa_circ_232719,RMVar_hsa_circ_296199,RMVar_hsa_circ_377588,RMVar_hsa_circ_332660,RMVar_hsa_circ_292846,RMVar_hsa_circ_232720,RMVar_hsa_circ_232717,RMVar_hsa_circ_232718,RMVar_hsa_circ_355131,RMVar_hsa_circ_305547,RMVar_hsa_circ_232721 69570 RMVar_ID_69570 Human_SNP_ID_238106481 m1A Human chr5 - 79427801 79427801 79427801 GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAAAGGAAGGAAGGAAGGAAATGAAGGAAAGGAAGG GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAAGGGAAGGAAGGAAGGAAATGAAGGAAAGGAAGG T C HOMER1 Ensembl:ENSG00000152413 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:79427750..79427838 26863196 MeRIP-seq:(Medium) rs1561359814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17069733 RMVar_hsa_circ_2953,RMVar_hsa_circ_232719,RMVar_hsa_circ_296199,RMVar_hsa_circ_377588,RMVar_hsa_circ_332660,RMVar_hsa_circ_292846,RMVar_hsa_circ_232720,RMVar_hsa_circ_232717,RMVar_hsa_circ_232718,RMVar_hsa_circ_355131,RMVar_hsa_circ_305547,RMVar_hsa_circ_232721 69571 RMVar_ID_69571 Human_SNP_ID_238127320 m1A Human chr5 + 79513936 79513936 79513936 TCACGCTCCGCGCCGCCGCCACGCGCCGCCTCACATTCCCCGGGCCCCGCCGCCGCCTCTTCACA TCACGCTCCGCGCCGCCGCCACGCGCCGCCTCGCATTCCCCGGGCCCCGCCGCCGCCTCTTCACA A G RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:79513720..79514105 26863196 MeRIP-seq:(Medium) rs952631815 Functional Loss SNV dbSNP153 33..33 33 - - - 69572 RMVar_ID_69572 Human_SNP_ID_238127575 m1A Human chr5 - 79514471 79514448 79514472 CGGAGGAGGCTGTGGCGGTCGGGAGCGGGGCCAAGAGCCAGAGGAGGAGCAGAGCGCACGGCCAG CGGAGGAGGCTGTGGCGGTCGGGAGCGGGGC________________________GCACGGCCAG CGCTCTGCTCCTCCTCTGGCTCTTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:79514428..79514499 26863196 MeRIP-seq:(Medium) rs1298181349 Functional Loss DEL dbSNP153 32..55 33 - - - 69573 RMVar_ID_69573 Human_SNP_ID_238127606 m1A Human chr5 + 79514491 79514491 79514491 TCCTCTGGCTCTTGGCCCCGCTCCCGACCGCCACAGCCTCCTCCGCGCCCCACACCAGGTGCTCG TCCTCTGGCTCTTGGCCCCGCTCCCGACCGCCCCAGCCTCCTCCGCGCCCCACACCAGGTGCTCG A C RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79514331..79514523 26863196 MeRIP-seq:(Medium) rs917758083 Functional Loss SNV dbSNP153 33..33 33 - - - 69574 RMVar_ID_69574 Human_SNP_ID_238152356 m1A Human chr5 + 79612529 79612529 79612529 TTCGGCGACTTTTTGCTCTTCCGCTTTTTGCCACCGCCCCCAACCTTCTATATCCTTGCAGCCCC TTCGGCGACTTTTTGCTCTTCCGCTTTTTGCCGCCGCCCCCAACCTTCTATATCCTTGCAGCCCC A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:79612483..79612559;chr5:79612480..79612796;chr5:79612479..79612594 26863196 MeRIP-seq:(Medium) rs376796493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845799,Human_RBP_ID_15524289,Human_RBP_ID_27084555 RMVar_hsa_circ_116764,RMVar_hsa_circ_232728 69575 RMVar_ID_69575 Human_SNP_ID_238157202 m1A Human chr5 + 79630618 79630618 79630618 TGGGGATGGGGAGACTGCTTTAGAGAGAGGAAATAGCATGTTTGAGGGTGTTGATGCAGAAAGGA TGGGGATGGGGAGACTGCTTTAGAGAGAGGAAGTAGCATGTTTGAGGGTGTTGATGCAGAAAGGA A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79630567..79630753 26863196 MeRIP-seq:(Medium) rs149082480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10223564,Human_RBP_ID_15525140 RMVar_hsa_circ_16464,RMVar_hsa_circ_116764,RMVar_hsa_circ_232728,RMVar_hsa_circ_63265,RMVar_hsa_circ_281438,RMVar_hsa_circ_350576,RMVar_hsa_circ_361680,RMVar_hsa_circ_66257,RMVar_hsa_circ_60940,RMVar_hsa_circ_232732,RMVar_hsa_circ_232736,RMVar_hsa_circ_336652,RMVar_hsa_circ_357324,RMVar_hsa_circ_373213,RMVar_hsa_circ_296811,RMVar_hsa_circ_292270,RMVar_hsa_circ_28905,RMVar_hsa_circ_62973,RMVar_hsa_circ_110147,RMVar_hsa_circ_60335,RMVar_hsa_circ_232738,RMVar_hsa_circ_232740,RMVar_hsa_circ_232739,RMVar_hsa_circ_232737,RMVar_hsa_circ_232746,RMVar_hsa_circ_71421,RMVar_hsa_circ_353107,RMVar_hsa_circ_72396,RMVar_hsa_circ_334278,RMVar_hsa_circ_363348,RMVar_hsa_circ_365815,RMVar_hsa_circ_352930,RMVar_hsa_circ_375927,RMVar_hsa_circ_362318,RMVar_hsa_circ_100498,RMVar_hsa_circ_342004,RMVar_hsa_circ_94775,RMVar_hsa_circ_232750,RMVar_hsa_circ_2035,RMVar_hsa_circ_37706,RMVar_hsa_circ_232751,RMVar_hsa_circ_232752,RMVar_hsa_circ_232748,RMVar_hsa_circ_232749,RMVar_hsa_circ_232747,RMVar_hsa_circ_232745 69576 RMVar_ID_69576 Human_SNP_ID_238159535 m1A Human chr5 - 79639662 79639662 79639662 CTCTAGAACCACAAGAGATCTAGATTCCCTTGAATCCTCCATTTTCTCCCAAGCCATCAGCATAA CTCTAGAACCACAAGAGATCTAGATTCCCTTGCATCCTCCATTTTCTCCCAAGCCATCAGCATAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79639617..79639689 26863196 MeRIP-seq:(Medium) rs1320433772 Functional Loss SNV dbSNP153 33..33 33 - - - 69577 RMVar_ID_69577 Human_SNP_ID_238243848 m1A Human chr5 - 79991206 79991206 79991206 ATGGCGGCCCCCTTGGAACTCAGTTGCTGGGGAGGCGGCTGGGGACTCCCATCGGTTCACAGCGA ATGGCGGCCCCCTTGGAACTCAGTTGCTGGGGTGGCGGCTGGGGACTCCCATCGGTTCACAGCGA T A MTX3 Ensembl:ENSG00000177034 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79990986..79991210 26863196 MeRIP-seq:(Medium) rs935520286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7476035,Human_RBP_ID_18053936,Human_RBP_ID_18424978,Human_RBP_ID_18449141 Human_Splice_Rec_667041,Human_Splice_Rec_667057,Human_Splice_Rec_667065,Human_Splice_Rec_667079 69578 RMVar_ID_69578 Human_SNP_ID_238310672 m1A Human chr5 - 80256502 80256502 80256502 CAGATGAGGGAAGGAAAGGGATTTCAGGAACAAGGATCTCGTGGGTGGGCTGTCCCAGTCGGCGC CAGATGAGGGAAGGAAAGGGATTTCAGGAACACGGATCTCGTGGGTGGGCTGTCCCAGTCGGCGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:80256453..80256536 26863196 MeRIP-seq:(Medium) rs1055858323 Functional Loss SNV dbSNP153 33..33 33 - - - 69579 RMVar_ID_69579 Human_SNP_ID_238361020 m1A Human chr5 + 80448220 80448220 80448220 GGTTCATTTACACTAGATGATGATGTTTTTGCAGAAACTGAAGAACCATCTAGTCCTACTGGTGT GGTTCATTTACACTAGATGATGATGTTTTTGCCGAAACTGAAGAACCATCTAGTCCTACTGGTGT A C ZFYVE16 Ensembl:ENSG00000039319 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:80448172..80448250 32194978 MeRIP-seq:(Medium) rs201166773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57515,RMVar_hsa_circ_58651,RMVar_hsa_circ_22911,RMVar_hsa_circ_339304,RMVar_hsa_circ_354557,RMVar_hsa_circ_359630,RMVar_hsa_circ_339601,RMVar_hsa_circ_268011,RMVar_hsa_circ_290196,RMVar_hsa_circ_232798,RMVar_hsa_circ_378045,RMVar_hsa_circ_31410,RMVar_hsa_circ_60124,RMVar_hsa_circ_11272,RMVar_hsa_circ_62726,RMVar_hsa_circ_367969,RMVar_hsa_circ_232802,RMVar_hsa_circ_232803,RMVar_hsa_circ_343287 69580 RMVar_ID_69580 Human_SNP_ID_238361021 m1A Human chr5 + 80448220 80448220 80448220 GGTTCATTTACACTAGATGATGATGTTTTTGCAGAAACTGAAGAACCATCTAGTCCTACTGGTGT GGTTCATTTACACTAGATGATGATGTTTTTGCGGAAACTGAAGAACCATCTAGTCCTACTGGTGT A G ZFYVE16 Ensembl:ENSG00000039319 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:80448172..80448250 32194978 MeRIP-seq:(Medium) rs201166773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57515,RMVar_hsa_circ_58651,RMVar_hsa_circ_22911,RMVar_hsa_circ_339304,RMVar_hsa_circ_354557,RMVar_hsa_circ_359630,RMVar_hsa_circ_339601,RMVar_hsa_circ_268011,RMVar_hsa_circ_290196,RMVar_hsa_circ_232798,RMVar_hsa_circ_378045,RMVar_hsa_circ_31410,RMVar_hsa_circ_60124,RMVar_hsa_circ_11272,RMVar_hsa_circ_62726,RMVar_hsa_circ_367969,RMVar_hsa_circ_232802,RMVar_hsa_circ_232803,RMVar_hsa_circ_343287 69581 RMVar_ID_69581 Human_SNP_ID_238370283 m1A Human chr5 - 80487822 80487797 80487822 CTGCGTTAGGGCATACTGCGGCGGAGGATGGAACTCCGATTGAAAGCAGTTGCTGGAGTGGAGCA CTGCGTTAGGGCATACTGCGGCGGAGGATGGA_________________________GTGGAGCA CTCCAGCAACTGCTTTCAATCGGAGT C AC008771.1 Ensembl:ENSG00000249042 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:80483067..80487821 32194978 MeRIP-seq:(Medium) rs1163686355 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_5616717,Human_RBP_ID_9399231,Human_RBP_ID_24118444 Human_Splice_Rec_667551,Human_Splice_Rec_667555,Human_Splice_Rec_667559 69582 RMVar_ID_69582 Human_SNP_ID_238370295 m1A Human chr5 - 80487870 80487870 80487870 CGCTCCTCCGAAAGGTTTCGGAAGCTGGTGGTAGCTCTGAAGATAACGCTGCGTTAGGGCATACT CGCTCCTCCGAAAGGTTTCGGAAGCTGGTGGTCGCTCTGAAGATAACGCTGCGTTAGGGCATACT T G AC008771.1 Ensembl:ENSG00000249042 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80487820..80488010 26863196 MeRIP-seq:(Medium) rs1382107612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5103678,Human_RBP_ID_5215192,Human_RBP_ID_9399231,Human_RBP_ID_24118446 Human_Splice_Rec_667551,Human_Splice_Rec_667555,Human_Splice_Rec_667559 69583 RMVar_ID_69583 Human_SNP_ID_238405629 m1A Human chr5 - 80627514 80627514 80627514 TGGCAAAGCCCCATCTCTACAAAAAACACAAAAATTAGCTGGGCATTGTGGCGCACACCTGTATT TGGCAAAGCCCCATCTCTACAAAAAACACAAAGATTAGCTGGGCATTGTGGCGCACACCTGTATT T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1461494593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26528526 69584 RMVar_ID_69584 Human_SNP_ID_238405728 m1A Human chr5 - 80627969 80627969 80627969 GAACTCGTGACCGCAAGCGATTCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG GAACTCGTGACCGCAAGCGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1278913894 Functional Loss SNV dbSNP153 33..33 33 - - - 69585 RMVar_ID_69585 Human_SNP_ID_238405745 m1A Human chr5 - 80628024 80628024 80628024 GTATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTAGTCTCGAACTCGTGA GTATTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGCTAGTCTCGAACTCGTGA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs879172237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647481,Human_RBP_ID_23194200 69586 RMVar_ID_69586 Human_SNP_ID_238405785 m1A Human chr5 - 80628179 80628179 80628179 TTAGACAGCGTTTCGCTCTTGTTGCCCAGGCTAGCATGCAATGGTGTGACCTCGGCTTACTGCAA TTAGACAGCGTTTCGCTCTTGTTGCCCAGGCTGGCATGCAATGGTGTGACCTCGGCTTACTGCAA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1178767396 Functional Loss SNV dbSNP153 33..33 33 - - - 69587 RMVar_ID_69587 Human_SNP_ID_238411282 m1A Human chr5 - 80650236 80650236 80650236 AAAGGTTAAAAAAAGTAAAAGGAACTCGGCAAACCTTACCCCACCTGTTTACCAAAAACATCACC AAAGGTTAAAAAAAGTAAAAGGAACTCGGCAACCCTTACCCCACCTGTTTACCAAAAACATCACC T G DHFR Ensembl:ENSG00000228716 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:80650071..80650257;chr5:80650133..80650368;chr5:80650063..80650287 26863196 MeRIP-seq:(Medium) rs984980566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17197527 RMVar_hsa_circ_54991,RMVar_hsa_circ_367945 69588 RMVar_ID_69588 Human_SNP_ID_238411287 m1A Human chr5 - 80650246 80650246 80650246 GCCCACAAGGAAAGGTTAAAAAAAGTAAAAGGAACTCGGCAAACCTTACCCCACCTGTTTACCAA GCCCACAAGGAAAGGTTAAAAAAAGTAAAAGGGACTCGGCAAACCTTACCCCACCTGTTTACCAA T C DHFR Ensembl:ENSG00000228716 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80650050..80650450 26863196 MeRIP-seq:(Medium) rs909287435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54991,RMVar_hsa_circ_367945 69589 RMVar_ID_69589 Human_SNP_ID_238411654 m1A Human chr5 - 80651446 80651446 80651446 ACCTCTTGCTCAGCCTATATACCGCCATCTTCAGCAAACCCTGACGAAGGCTGCAAAGTAAGCGC ACCTCTTGCTCAGCCTATATACCGCCATCTTCGGCAAACCCTGACGAAGGCTGCAAAGTAAGCGC T C DHFR Ensembl:ENSG00000228716 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:80651409..80651670 26863410 MeRIP-seq:(Medium) rs1211865963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251012,Human_RBP_ID_789395,Human_RBP_ID_1658697,Human_RBP_ID_5242469,Human_RBP_ID_17671614,Human_RBP_ID_18054077,Human_RBP_ID_21900579,Human_RBP_ID_22426573,Human_RBP_ID_22458875,Human_RBP_ID_22481916,Human_RBP_ID_22531742 RMVar_hsa_circ_54991,RMVar_hsa_circ_367945 69590 RMVar_ID_69590 Human_SNP_ID_238412633 m1A Human chr5 + 80654598 80654564 80654599 CCCCGCCCCCCTCGTCCCCATTTGTGCAGGCGAGGCCCCGCCCCCCCGCCCCGGCGCACGCAGGG __________________________________GCCCCGCCCCCCCGCCCCGGCGCACGCAGGG CGCCCCGCCCCCCTCGTCCCCATTTGTGCAGGCGAG C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:80654523..80654610 26863410 MeRIP-seq:(Medium) rs1464445339 Functional Loss DEL dbSNP153 1..34 33 - - - 69591 RMVar_ID_69591 Human_SNP_ID_238412760 m1A Human chr5 + 80654693 80654692 80654693 GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCAGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCC_GGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG CA C MSH3 Ensembl:ENSG00000113318 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs765543063 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4845808 69592 RMVar_ID_69592 Human_SNP_ID_238412764 m1A Human chr5 + 80654693 80654693 80654693 GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCAGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCGGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG A G MSH3 Ensembl:ENSG00000113318 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1105524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845808 69593 RMVar_ID_69593 Human_SNP_ID_238412765 m1A Human chr5 + 80654693 80654693 80654693 GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCAGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCTGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG A T MSH3 Ensembl:ENSG00000113318 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1105524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845808 69594 RMVar_ID_69594 Human_SNP_ID_238412870 m1A Human chr5 + 80654850 80654850 80654850 ACGGGAAGCCTGAAATCCACCTCCTCCTCCACAGGTGCAGCCGACCAGGTGGACCCTGGCGCTGC ACGGGAAGCCTGAAATCCACCTCCTCCTCCACGGGTGCAGCCGACCAGGTGGACCCTGGCGCTGC A G MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:80654749..80654895 26863410 MeRIP-seq:(Medium) rs751264470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845810,Human_RBP_ID_5476944,Human_RBP_ID_18449151 69595 RMVar_ID_69595 Human_SNP_ID_238412887 m1A Human chr5 + 80654870 80654870 80654870 CTCCTCCTCCACAGGTGCAGCCGACCAGGTGGACCCTGGCGCTGCAGCGGCTGCAGCGGCCGCAG CTCCTCCTCCACAGGTGCAGCCGACCAGGTGGCCCCTGGCGCTGCAGCGGCTGCAGCGGCCGCAG A C MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:80654697..80654925 26863410 MeRIP-seq:(Medium) rs773388641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250651 Human_Splice_Rec_667689,Human_Splice_Rec_667735,Human_Splice_Rec_667779 69596 RMVar_ID_69596 Human_SNP_ID_238412994 m1A Human chr5 + 80654910 80654910 80654910 GCTGCAGCGGCTGCAGCGGCCGCAGCGGCCGCAGCGCCCCCAGCGCCCCCAGCTCCCGCCTTCCC GCTGCAGCGGCTGCAGCGGCCGCAGCGGCCGCTGCGCCCCCAGCGCCCCCAGCTCCCGCCTTCCC A T MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:80654685..80655231;chr5:80654722..80654987 26863196 MeRIP-seq:(Medium) rs1448955835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_667689,Human_Splice_Rec_667735,Human_Splice_Rec_667779 69597 RMVar_ID_69597 Human_SNP_ID_238413001 m1A Human chr5 + 80654919 80654913 80654919 GCTGCAGCGGCCGCAGCGGCCGCAGCGCCCCCAGCGCCCCCAGCTCCCGCCTTCCCGCCCCAGCT GCTGCAGCGGCCGCAGCGGCCGCAGCG______GCGCCCCCAGCTCCCGCCTTCCCGCCCCAGCT GCCCCCA G MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:80654845..80654945 26863410 MeRIP-seq:(Medium) rs773624233 Functional Loss DEL dbSNP153 28..33 33 - - - Human_Splice_Rec_667689,Human_Splice_Rec_667735,Human_Splice_Rec_667779 69598 RMVar_ID_69598 Human_SNP_ID_238413016 m1A Human chr5 + 80654919 80654919 80654919 GCTGCAGCGGCCGCAGCGGCCGCAGCGCCCCCAGCGCCCCCAGCTCCCGCCTTCCCGCCCCAGCT GCTGCAGCGGCCGCAGCGGCCGCAGCGCCCCCGGCGCCCCCAGCTCCCGCCTTCCCGCCCCAGCT A G MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:80654845..80654945 26863410 MeRIP-seq:(Medium) rs1283888431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_667689,Human_Splice_Rec_667735,Human_Splice_Rec_667779 69599 RMVar_ID_69599 Human_SNP_ID_238421404 m1A Human chr5 + 80687584 80687584 80687584 GAAGGCTTTGAGTTGGTAATGGGGAGGGGGGAAGGGTATGTTGTGTGTGTATGGAAATGATATGA GAAGGCTTTGAGTTGGTAATGGGGAGGGGGGACGGGTATGTTGTGTGTGTATGGAAATGATATGA A C MSH3 Ensembl:ENSG00000113318 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80687571..80687653 26863196 MeRIP-seq:(Medium) rs755359365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7476922,Human_RBP_ID_24118559 RMVar_hsa_circ_415,RMVar_hsa_circ_37046,RMVar_hsa_circ_25607,RMVar_hsa_circ_350472,RMVar_hsa_circ_355376,RMVar_hsa_circ_29050,RMVar_hsa_circ_94131,RMVar_hsa_circ_24391,RMVar_hsa_circ_232819,RMVar_hsa_circ_232822,RMVar_hsa_circ_51214,RMVar_hsa_circ_285526,RMVar_hsa_circ_317833,RMVar_hsa_circ_41042,RMVar_hsa_circ_348336,RMVar_hsa_circ_369185,RMVar_hsa_circ_319071,RMVar_hsa_circ_300754,RMVar_hsa_circ_317523,RMVar_hsa_circ_298426,RMVar_hsa_circ_53882,RMVar_hsa_circ_68781,RMVar_hsa_circ_7212,RMVar_hsa_circ_232824,RMVar_hsa_circ_232826,RMVar_hsa_circ_232827,RMVar_hsa_circ_232825 69600 RMVar_ID_69600 Human_SNP_ID_238421731 m1A Human chr5 + 80689056 80689056 80689056 TGCCTAAATTAGGTGGGAAGGTGGGACTGGGTAGAAAGAGGGCATTCCAGGAAGTGTGGTCACAG TGCCTAAATTAGGTGGGAAGGTGGGACTGGGTGGAAAGAGGGCATTCCAGGAAGTGTGGTCACAG A G MSH3 Ensembl:ENSG00000113318 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80689036..80689175 26863196 MeRIP-seq:(Medium) rs1039855289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7476927 RMVar_hsa_circ_415,RMVar_hsa_circ_37046,RMVar_hsa_circ_25607,RMVar_hsa_circ_350472,RMVar_hsa_circ_355376,RMVar_hsa_circ_29050,RMVar_hsa_circ_94131,RMVar_hsa_circ_24391,RMVar_hsa_circ_232819,RMVar_hsa_circ_232822,RMVar_hsa_circ_51214,RMVar_hsa_circ_285526,RMVar_hsa_circ_317833,RMVar_hsa_circ_41042,RMVar_hsa_circ_348336,RMVar_hsa_circ_369185,RMVar_hsa_circ_319071,RMVar_hsa_circ_300754,RMVar_hsa_circ_317523,RMVar_hsa_circ_298426,RMVar_hsa_circ_53882,RMVar_hsa_circ_68781,RMVar_hsa_circ_7212,RMVar_hsa_circ_232824,RMVar_hsa_circ_232826,RMVar_hsa_circ_232827,RMVar_hsa_circ_232825 69601 RMVar_ID_69601 Human_SNP_ID_238448079 m1A Human chr5 + 80793621 80793621 80793621 TATTGAAGGGGAGTATTCCAGGTAGAAGAACCAGCATGGCAGATATTGGAAGTGAAGCATAGCAG TATTGAAGGGGAGTATTCCAGGTAGAAGAACCCGCATGGCAGATATTGGAAGTGAAGCATAGCAG A C MSH3 Ensembl:ENSG00000113318 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80793619..80793735 26863196 MeRIP-seq:(Medium) rs1453619189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_415,RMVar_hsa_circ_317833,RMVar_hsa_circ_317523,RMVar_hsa_circ_7212,RMVar_hsa_circ_232842,RMVar_hsa_circ_232827,RMVar_hsa_circ_327683,RMVar_hsa_circ_232829,RMVar_hsa_circ_74930,RMVar_hsa_circ_308260,RMVar_hsa_circ_232839,RMVar_hsa_circ_278484,RMVar_hsa_circ_282551,RMVar_hsa_circ_51628,RMVar_hsa_circ_232840,RMVar_hsa_circ_232841,RMVar_hsa_circ_232850,RMVar_hsa_circ_283876,RMVar_hsa_circ_232851,RMVar_hsa_circ_232853,RMVar_hsa_circ_307473,RMVar_hsa_circ_232854,RMVar_hsa_circ_232856,RMVar_hsa_circ_285731 69602 RMVar_ID_69602 Human_SNP_ID_238553318 m1A Human chr5 - 81238668 81238668 81238668 GAGGCAGGAGCCATGAGTGGCAGAGGCAGGGGAGGGACTGCAGAGACAGGTTGGAGCCAAAGCAC GAGGCAGGAGCCATGAGTGGCAGAGGCAGGGGGGGGACTGCAGAGACAGGTTGGAGCCAAAGCAC T C CKMT2-AS1 Ensembl:ENSG00000247572 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:81238621..81238753 26863196 MeRIP-seq:(Medium) rs200040414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612966,Human_RBP_ID_7477617,Human_RBP_ID_15531679 69603 RMVar_ID_69603 Human_SNP_ID_238568968 m1A Human chr5 + 81301436 81301436 81301436 CGTCTATCTCGCCTGCTACACTGTGAGTTCAGACAGCACGGATTGAACTCTTCATCTTTTCGTGT CGTCTATCTCGCCTGCTACACTGTGAGTTCAGGCAGCACGGATTGAACTCTTCATCTTTTCGTGT A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:81301359..81301485 26863196 MeRIP-seq:(Medium) rs1348459606 Functional Loss SNV dbSNP153 33..33 33 - - - 69604 RMVar_ID_69604 Human_SNP_ID_238569945 m1A Human chr5 + 81305083 81305083 81305083 AGTAAGGGAAGAAATTGCAGTTGCTTTAAAGAAAGACAGTCGACGGGAAGGAAGAAGATTAAAAA AGTAAGGGAAGAAATTGCAGTTGCTTTAAAGAGAGACAGTCGACGGGAAGGAAGAAGATTAAAAA A G ZCCHC9 Ensembl:ENSG00000131732 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:81304926..81305150 26863196 MeRIP-seq:(Medium) rs1194348185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2947661,Human_RBP_ID_5611270,Human_RBP_ID_7477879,Human_RBP_ID_23116249,Human_RBP_ID_26351012 Human_Splice_Rec_668213,Human_Splice_Rec_668229,Human_Splice_Rec_668247,Human_Splice_Rec_668257 RMVar_hsa_circ_358235 69605 RMVar_ID_69605 Human_SNP_ID_238674538 m1A Human chr5 - 81750049 81750049 81750049 TTTTGTGAGGCTGGCAGCCCCCGAGCGGCGGGAGGGGCGGGCCCGGCGGGGCGGTGGTCGGGGGC TTTTGTGAGGCTGGCAGCCCCCGAGCGGCGGGGGGGGCGGGCCCGGCGGGGCGGTGGTCGGGGGC T C SSBP2 Ensembl:ENSG00000145687 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:81750036..81750202 26863196 MeRIP-seq:(Medium) rs1001643638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232926,RMVar_hsa_circ_119581 69606 RMVar_ID_69606 Human_SNP_ID_238674787 m1A Human chr5 - 81750585 81750585 81750585 CGCCGGGGGTGGCGGGAGGGGCAGCTGCGTGGAGGAAGGCGCGCAGTGGGAATGTGGGTGTTTGG CGCCGGGGGTGGCGGGAGGGGCAGCTGCGTGGCGGAAGGCGCGCAGTGGGAATGTGGGTGTTTGG T G SSBP2 Ensembl:ENSG00000145687 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:81750399..81750603 26863196 MeRIP-seq:(Medium) rs1448338829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267096,Human_RBP_ID_8136607 RMVar_hsa_circ_232926,RMVar_hsa_circ_119581 69607 RMVar_ID_69607 Human_SNP_ID_238674842 m1A Human chr5 - 81750743 81750743 81750743 GGGGCTGTCGGCGGGAGGGACCGGGTGTGTTGAGGGGCGGCGGTGGTGCTGGTGGCGAGGATGGA GGGGCTGTCGGCGGGAGGGACCGGGTGTGTTGGGGGGCGGCGGTGGTGCTGGTGGCGAGGATGGA T C SSBP2 Ensembl:ENSG00000145687 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:81750737..81750808 26863196 MeRIP-seq:(Medium) rs1447026609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267020,Human_RBP_ID_3782773,Human_RBP_ID_5242255,Human_RBP_ID_8136892,Human_RBP_ID_8213491,Human_RBP_ID_8236682,Human_RBP_ID_9436688,Human_RBP_ID_18501734,Human_RBP_ID_19127263,Human_RBP_ID_22727352,Human_RBP_ID_26771518 Human_Splice_Rec_668671 RMVar_hsa_circ_232926,RMVar_hsa_circ_119581 69608 RMVar_ID_69608 Human_SNP_ID_238797132 m1A Human chr5 + 82277679 82277679 82277679 CGAATTCCTATAATAAACTAAAACTTGACGGGAGCAATGGACTTACACTTTTTCCAGCACGATTC CGAATTCCTATAATAAACTAAAACTTGACGGGGGCAATGGACTTACACTTTTTCCAGCACGATTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:82277676..82277700 26863196 MeRIP-seq:(Medium) rs949543097 Functional Loss SNV dbSNP153 33..33 33 - - - 69609 RMVar_ID_69609 Human_SNP_ID_238797167 m1A Human chr5 + 82277827 82277827 82277827 TTCTGGTCTCGTCGGTGACTACGGAGCTTCCTAGCAGTACGAAGTCCACGACACTTGCCTAAAAA TTCTGGTCTCGTCGGTGACTACGGAGCTTCCTGGCAGTACGAAGTCCACGACACTTGCCTAAAAA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr5:82277726..82277900;chr5:82277776..82277875 26863410,32194978 MeRIP-seq:(Medium) rs1409572075 Functional Loss SNV dbSNP153 33..33 33 - - - 69610 RMVar_ID_69610 Human_SNP_ID_238797180 m1A Human chr5 - 82277860 82277860 82277860 GGCGTGTTTTTACGGAAGAACTAAAATATTTAATTTTTAGGCAAGTGTCGTGGACTTCGTACTGC GGCGTGTTTTTACGGAAGAACTAAAATATTTAGTTTTTAGGCAAGTGTCGTGGACTTCGTACTGC T C RPS23 Ensembl:ENSG00000186468 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:82277851..82277875 26863196 MeRIP-seq:(Medium) rs1327584878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1323039 69611 RMVar_ID_69611 Human_SNP_ID_238797321 m1A Human chr5 - 82278204 82278204 82278204 GCGGGGGATGCCATGGAGAGGCTCCATGGGGGAGGGCCGGGGAAGCGCCGCTCCAGGAGGCACGT GCGGGGGATGCCATGGAGAGGCTCCATGGGGGGGGGCCGGGGAAGCGCCGCTCCAGGAGGCACGT T C RPS23 Ensembl:ENSG00000186468 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:82278181..82278325 26863196 MeRIP-seq:(Medium) rs1431351647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647712,Human_RBP_ID_5397320,Human_RBP_ID_8213168,Human_RBP_ID_9436544,Human_RBP_ID_18956033,Human_RBP_ID_26791857 69612 RMVar_ID_69612 Human_SNP_ID_238797372 m1A Human chr5 + 82278308 82278308 82278308 CAAGTCCCGCTTGCAGCGCCCTTAAACCGGCCACAACAGCTCACCCATCCTGTCGGCGCCACGGG CAAGTCCCGCTTGCAGCGCCCTTAAACCGGCCCCAACAGCTCACCCATCCTGTCGGCGCCACGGG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr5:82278301..82278350;chr5:82278301..82278375 32194978 MeRIP-seq:(Medium) rs1417622179 Functional Loss SNV dbSNP153 33..33 33 - - - 69613 RMVar_ID_69613 Human_SNP_ID_238990163 m1A Human chr5 + 83077227 83077227 83077227 ACATGGCTCCAAGGCCTCTCAGCTCCGGGCCCACACACCCCGGGCTGCCGCACAAACTCCAGCCC ACATGGCTCCAAGGCCTCTCAGCTCCGGGCCCTCACACCCCGGGCTGCCGCACAAACTCCAGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:83077221..83077369 26863196 MeRIP-seq:(Medium) rs1461226569 Functional Loss SNV dbSNP153 33..33 33 - - - 69614 RMVar_ID_69614 Human_SNP_ID_238990174 m1A Human chr5 - 83077260 83077260 83077260 TGATCTTCGAGAAGGGGTTGTGGATCTAGACTAGGGCTGGAGTTTGTGCGGCAGCCCGGGGTGTG TGATCTTCGAGAAGGGGTTGTGGATCTAGACTGGGGCTGGAGTTTGTGCGGCAGCCCGGGGTGTG T C TMEM167A Ensembl:ENSG00000174695 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:83077258..83077345 26863196 MeRIP-seq:(Medium) rs36209438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788420,Human_RBP_ID_5396676,Human_RBP_ID_7479680,Human_RBP_ID_15536341,Human_RBP_ID_19127266,Human_RBP_ID_22364882 RMVar_hsa_circ_107589,RMVar_hsa_circ_232956 69615 RMVar_ID_69615 Human_SNP_ID_238990176 m1A Human chr5 + 83077268 83077268 83077268 GGGCTGCCGCACAAACTCCAGCCCTAGTCTAGATCCACAACCCCTTCTCGAAGATCAACCGCGAC GGGCTGCCGCACAAACTCCAGCCCTAGTCTAGTTCCACAACCCCTTCTCGAAGATCAACCGCGAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:83077265..83077389 26863196 MeRIP-seq:(Medium) rs1421303425 Functional Loss SNV dbSNP153 33..33 33 - - - 69616 RMVar_ID_69616 Human_SNP_ID_239299837 m1A Human chr5 - 84384764 84384764 84384764 GTCAGAAGCCCCGCAGCCGCCGCGCGGAGAACAGCGACAGCCGAGCGCCCGGTCCGCCTGTCTGC GTCAGAAGCCCCGCAGCCGCCGCGCGGAGAACGGCGACAGCCGAGCGCCCGGTCCGCCTGTCTGC T C EDIL3 Ensembl:ENSG00000164176 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:84384551..84384909 26863196 MeRIP-seq:(Medium) rs926309458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98891,RMVar_hsa_circ_232989 69617 RMVar_ID_69617 Human_SNP_ID_239866673 m1A Human chr5 + 86618005 86618005 86618005 CGTGAAAAAAAAGGTCTTGGTGAGGTGCCGCCATTTCATCTGTCCTCATTCTCTGCGCCTTTCGC CGTGAAAAAAAAGGTCTTGGTGAGGTGCCGCCGTTTCATCTGTCCTCATTCTCTGCGCCTTTCGC A G COX7C Ensembl:ENSG00000127184 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:86617926..86618162 26863196 MeRIP-seq:(Medium) rs769868698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270674,Human_RBP_ID_648032,Human_RBP_ID_1213967,Human_RBP_ID_1659184,Human_RBP_ID_2001106,Human_RBP_ID_3780047,Human_RBP_ID_4845246,Human_RBP_ID_5212822,Human_RBP_ID_5326512,Human_RBP_ID_5427552,Human_RBP_ID_5450134,Human_RBP_ID_5477178,Human_RBP_ID_5509986,Human_RBP_ID_5532212,Human_RBP_ID_7481181,Human_RBP_ID_8623818,Human_RBP_ID_9335256,Human_RBP_ID_15537249,Human_RBP_ID_17301679,Human_RBP_ID_17414934,Human_RBP_ID_17531854,Human_RBP_ID_17662877,Human_RBP_ID_18055003,Human_RBP_ID_18210810,Human_RBP_ID_18848528,Human_RBP_ID_21204429,Human_RBP_ID_22303320,Human_RBP_ID_22458878,Human_RBP_ID_22771383,Human_RBP_ID_22828943,Human_RBP_ID_24120122,Human_RBP_ID_26531208,Human_RBP_ID_26826419,Human_RBP_ID_27085016,Human_RBP_ID_27338839,Human_RBP_ID_27517655 Human_Splice_Rec_669375,Human_Splice_Rec_669379,Human_Splice_Rec_669395 Human_miRNA_ID_1961704 RMVar_hsa_circ_90702,RMVar_hsa_circ_232990 69618 RMVar_ID_69618 Human_SNP_ID_239867092 m1A Human chr5 + 86619303 86619303 86619303 TTTCCTGTATACTTGTATTTTGATTATTAAGCAGATGATTTGAGATTCAATTTCGATTACTTTTT TTTCCTGTATACTTGTATTTTGATTATTAAGCGGATGATTTGAGATTCAATTTCGATTACTTTTT A G COX7C Ensembl:ENSG00000127184 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:86619300..86619480 26863196 MeRIP-seq:(Medium) rs1016273194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17629038 RMVar_hsa_circ_90702,RMVar_hsa_circ_232990 69619 RMVar_ID_69619 Human_SNP_ID_240028161 m1A Human chr5 + 87268473 87268473 87268473 CGGGCTTCAACATGATGGCGGCCGAGGCCGGCAGTGAGGAGGGCGGCCCGGTAACAGCCGGAGCT CGGGCTTCAACATGATGGCGGCCGAGGCCGGCCGTGAGGAGGGCGGCCCGGTAACAGCCGGAGCT A C RASA1 Ensembl:ENSG00000145715 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:87267937..87268808;chr5:87267998..87268835 26863196 MeRIP-seq:(Medium) rs1176105751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250757,Human_RBP_ID_1109387,Human_RBP_ID_3967283,Human_RBP_ID_4845247,Human_RBP_ID_5326514,Human_RBP_ID_5477083,Human_RBP_ID_18425135,Human_RBP_ID_24120254 69620 RMVar_ID_69620 Human_SNP_ID_240269592 m1A Human chr5 - 88269072 88269072 88269072 TGCGTTCCTGTTGAAACCACCCAATCTACCTCAGGGTCCTCGCAAGCGCAGCCACCACGATCCGC TGCGTTCCTGTTGAAACCACCCAATCTACCTCGGGGTCCTCGCAAGCGCAGCCACCACGATCCGC T C TMEM161B Ensembl:ENSG00000164180 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:88268940..88269139 26863196 MeRIP-seq:(Medium) rs1448029766 Functional Loss SNV dbSNP153 33..33 33 - - - 69621 RMVar_ID_69621 Human_SNP_ID_667085763 m1A Human chr19 + 45040749 45040749 45040749 GCTCACGCCTGTAATCCCAAGTGGATCACCTGAGGTCACGAGTTCGAGACCAGCCTGGCCAAAAG GCTCACGCCTGTAATCCCAAGTGGATCACCTGTGGTCACGAGTTCGAGACCAGCCTGGCCAAAAG A T CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:45040746..45052945 26863196 MeRIP-seq:(Medium) rs1006347045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25424558 RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 69622 RMVar_ID_69622 Human_SNP_ID_667088150 m1A Human chr19 + 45049938 45049938 45049938 GTTAAGTGAGTGAATTGTGTGGTATATGAATTACTTCTCAATAAAGCCACAGAGTGAAGGAGCTG GTTAAGTGAGTGAATTGTGTGGTATATGAATTGCTTCTCAATAAAGCCACAGAGTGAAGGAGCTG A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45049934..45050144 26863196 MeRIP-seq:(Medium) rs1023019748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 69623 RMVar_ID_69623 Human_SNP_ID_667088902 m1A Human chr19 + 45052870 45052870 45052870 TCCGTGCCCACCTGGACCACATCCCCGACTACACCCCCCCTCTGCTCACCACCATGTAAGCCACC TCCGTGCCCACCTGGACCACATCCCCGACTACGCCCCCCCTCTGCTCACCACCATGTAAGCCACC A G CLASRP Ensembl:ENSG00000104859 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45052851..45052875 26863196 MeRIP-seq:(Medium) rs766032837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523456,Human_RBP_ID_912461 Human_Splice_Rec_2018286,Human_Splice_Rec_2018287,Human_Splice_Rec_2018364,Human_Splice_Rec_2018380,Human_Splice_Rec_2018381,Human_Splice_Rec_2018422,Human_Splice_Rec_2018426,Human_Splice_Rec_2018427,Human_Splice_Rec_2018462,Human_Splice_Rec_2018463 RMVar_hsa_circ_6134,RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277,RMVar_hsa_circ_195278,RMVar_hsa_circ_293265,RMVar_hsa_circ_303238,RMVar_hsa_circ_195279,RMVar_hsa_circ_108920,RMVar_hsa_circ_304926,RMVar_hsa_circ_195281,RMVar_hsa_circ_195282,RMVar_hsa_circ_195280 69624 RMVar_ID_69624 Human_SNP_ID_667088903 m1A Human chr19 + 45052870 45052870 45052870 TCCGTGCCCACCTGGACCACATCCCCGACTACACCCCCCCTCTGCTCACCACCATGTAAGCCACC TCCGTGCCCACCTGGACCACATCCCCGACTACTCCCCCCCTCTGCTCACCACCATGTAAGCCACC A T CLASRP Ensembl:ENSG00000104859 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45052851..45052875 26863196 MeRIP-seq:(Medium) rs766032837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523456,Human_RBP_ID_912461 Human_Splice_Rec_2018286,Human_Splice_Rec_2018287,Human_Splice_Rec_2018364,Human_Splice_Rec_2018380,Human_Splice_Rec_2018381,Human_Splice_Rec_2018422,Human_Splice_Rec_2018426,Human_Splice_Rec_2018427,Human_Splice_Rec_2018462,Human_Splice_Rec_2018463 RMVar_hsa_circ_6134,RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277,RMVar_hsa_circ_195278,RMVar_hsa_circ_293265,RMVar_hsa_circ_303238,RMVar_hsa_circ_195279,RMVar_hsa_circ_108920,RMVar_hsa_circ_304926,RMVar_hsa_circ_195281,RMVar_hsa_circ_195282,RMVar_hsa_circ_195280 69625 RMVar_ID_69625 Human_SNP_ID_667091986 m1A Human chr19 - 45064037 45064037 45064037 GCCCGGGGTCGGGGAGCGGGAGCGGGAGCGGGACTCTGAGCTGGACTCCGAGGGTGACCTGCGGG GCCCGGGGTCGGGGAGCGGGAGCGGGAGCGGGGCTCTGAGCTGGACTCCGAGGGTGACCTGCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45059337..45068127 32194978 MeRIP-seq:(Medium) rs199673955 Functional Loss SNV dbSNP153 33..33 33 - - - 69626 RMVar_ID_69626 Human_SNP_ID_667092070 m1A Human chr19 - 45064183 45064183 45064183 TTACGTCCCGGGGCGGGGCCGCCAGGCTGGGGAGGTGCGGGGGGCTTCCCTGTGGTGACTCCTGA TTACGTCCCGGGGCGGGGCCGCCAGGCTGGGGTGGTGCGGGGGGCTTCCCTGTGGTGACTCCTGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45064088..45064188 26863410 MeRIP-seq:(Medium) rs776963253 Functional Loss SNV dbSNP153 33..33 33 - - - 69627 RMVar_ID_69627 Human_SNP_ID_667092071 m1A Human chr19 - 45064183 45064183 45064183 TTACGTCCCGGGGCGGGGCCGCCAGGCTGGGGAGGTGCGGGGGGCTTCCCTGTGGTGACTCCTGA TTACGTCCCGGGGCGGGGCCGCCAGGCTGGGGGGGTGCGGGGGGCTTCCCTGTGGTGACTCCTGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45064088..45064188 26863410 MeRIP-seq:(Medium) rs776963253 Functional Loss SNV dbSNP153 33..33 33 - - - 69628 RMVar_ID_69628 Human_SNP_ID_667092211 m1A Human chr19 - 45064368 45064368 45064368 GCGGGAGCTGGAGGTCCTCGAGGCAGAAGAGGAGGAGGAGGAGGAGGAGGAGCGGCGGCTGCAGG GCGGGAGCTGGAGGTCCTCGAGGCAGAAGAGGTGGAGGAGGAGGAGGAGGAGCGGCGGCTGCAGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:45064230..45064375 26863196 MeRIP-seq:(Medium) rs1266421015 Functional Loss SNV dbSNP153 33..33 33 - - - 69629 RMVar_ID_69629 Human_SNP_ID_667093375 m1A Human chr19 + 45067538 45067538 45067538 AGCCGCAGCCAGAGCCCCTCGCCATCACCCGCAAGAGAGAAGCTGACCAGGCCGGCCGCGTCCCC AGCCGCAGCCAGAGCCCCTCGCCATCACCCGCGAGAGAGAAGCTGACCAGGCCGGCCGCGTCCCC A G CLASRP Ensembl:ENSG00000104859 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45067457..45067557 26863410 MeRIP-seq:(Medium) rs1292891260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137452,Human_RBP_ID_9381118,Human_RBP_ID_18998088,Human_RBP_ID_23114823,Human_RBP_ID_27816514 Human_Splice_Rec_2018307,Human_Splice_Rec_2018345,Human_Splice_Rec_2018401,Human_Splice_Rec_2018447,Human_Splice_Rec_2018483 RMVar_hsa_circ_100916,RMVar_hsa_circ_195276 69630 RMVar_ID_69630 Human_SNP_ID_667094481 m1A Human chr19 - 45070758 45070758 45070758 AGGGAGGGGCCGTGAGGATGGGGCATACACACATCAACACACCTGGGGCCGTGGATGCTTCAGTG AGGGAGGGGCCGTGAGGATGGGGCATACACACTTCAACACACCTGGGGCCGTGGATGCTTCAGTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45070756..45070844 26863196 MeRIP-seq:(Medium) rs752217782 Functional Loss SNV dbSNP153 33..33 33 - - - 69631 RMVar_ID_69631 Human_SNP_ID_667096378 m1A Human chr19 - 45076311 45076311 45076311 CGCCGAGTAGAGCCCGCGCCCGCCGCCAACCCAGACGACGAGATGGAAATGCAGGACCTCGTCAT CGCCGAGTAGAGCCCGCGCCCGCCGCCAACCCGGACGACGAGATGGAAATGCAGGACCTCGTCAT T C ZNF296 Ensembl:ENSG00000170684 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45076268..45076466 26863196 MeRIP-seq:(Medium) rs1348431228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4536279,Human_RBP_ID_27469026 69632 RMVar_ID_69632 Human_SNP_ID_667096389 m1A Human chr19 + 45076336 45076336 45076336 CGTCGTCTGGGTTGGCGGCGGGCGCGGGCTCTACTCGGCGGGGCGCGCTGCCGGCCTTGCGGCGG CGTCGTCTGGGTTGGCGGCGGGCGCGGGCTCTGCTCGGCGGGGCGCGCTGCCGGCCTTGCGGCGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45076224..45076433 26863196 MeRIP-seq:(Medium) rs367602377 Functional Loss SNV dbSNP153 33..33 33 - - - 69633 RMVar_ID_69633 Human_SNP_ID_667096429 m1A Human chr19 + 45076414 45076414 45076414 GGCCGGGCGAGCGAGCGGGCGGGCAGGCAGGCAGGCGGGCGGGCGGAGGACGCACGAGCGGAGGA GGCCGGGCGAGCGAGCGGGCGGGCAGGCAGGCGGGCGGGCGGGCGGAGGACGCACGAGCGGAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:45075826..45076463;chr19:45076222..45076453 26863196 MeRIP-seq:(Medium) rs1450502888 Functional Loss SNV dbSNP153 33..33 33 - - - 69634 RMVar_ID_69634 Human_SNP_ID_667098009 m1A Human chr19 + 45081919 45081919 45081919 TGCTGGGATTACAGGCGTGACCTACTGCGCCCAGCCTCGACCTTTCAAACATAGCCTAATCTGAC TGCTGGGATTACAGGCGTGACCTACTGCGCCCGGCCTCGACCTTTCAAACATAGCCTAATCTGAC A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:45081870..45082051 26863196 MeRIP-seq:(Medium) rs1213433519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13473648,Human_RBP_ID_20403321 69635 RMVar_ID_69635 Human_SNP_ID_667101364 m1A Human chr19 + 45093222 45093222 45093222 CCACTAGGAGAGCGGACGGAGGCGGCGCCTGAAGCGGCGGCGGAGCCCATGCCCCGGGACGGCGG CCACTAGGAGAGCGGACGGAGGCGGCGCCTGAGGCGGCGGCGGAGCCCATGCCCCGGGACGGCGG A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45093160..45093517 26863196 MeRIP-seq:(Medium) rs1486057800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773247,Human_RBP_ID_4557591,Human_RBP_ID_5527045,Human_RBP_ID_18421419,Human_RBP_ID_18995105,Human_RBP_ID_23119207,Human_RBP_ID_27816522 RMVar_hsa_circ_267348 69636 RMVar_ID_69636 Human_SNP_ID_667101370 m1A Human chr19 + 45093233 45093233 45093233 GCGGACGGAGGCGGCGCCTGAAGCGGCGGCGGAGCCCATGCCCCGGGACGGCGGGCGGACCCGGA GCGGACGGAGGCGGCGCCTGAAGCGGCGGCGGGGCCCATGCCCCGGGACGGCGGGCGGACCCGGA A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45093160..45093509 26863196 MeRIP-seq:(Medium) rs1237837677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824422,Human_RBP_ID_4557591,Human_RBP_ID_5527045,Human_RBP_ID_18421419,Human_RBP_ID_18995105,Human_RBP_ID_23119207,Human_RBP_ID_27816522 RMVar_hsa_circ_267348 69637 RMVar_ID_69637 Human_SNP_ID_667103017 m1A Human chr19 - 45099095 45099095 45099095 GCTATAGGTGGGGGCAGAGGAGTGGTGATGACAGGAATAACAAGGGAGGCATTTGCTGGGCATTT GCTATAGGTGGGGGCAGAGGAGTGGTGATGACCGGAATAACAAGGGAGGCATTTGCTGGGCATTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45099093..45099187 26863196 MeRIP-seq:(Medium) rs1444126815 Functional Loss SNV dbSNP153 33..33 33 - - - 69638 RMVar_ID_69638 Human_SNP_ID_667103552 m1A Human chr19 - 45101163 45101163 45101163 TCTAGGAAGCTGCCTCTGCCCTGCCCTCCTGCACACCCTGTGGACCCTCCCTAATCTGAGTCCTC TCTAGGAAGCTGCCTCTGCCCTGCCCTCCTGCCCACCCTGTGGACCCTCCCTAATCTGAGTCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45101158..45101332 26863196 MeRIP-seq:(Medium) rs1251444891 Functional Loss SNV dbSNP153 33..33 33 - - - 69639 RMVar_ID_69639 Human_SNP_ID_667114511 m1A Human chr19 - 45142413 45142413 45142413 GTGGTTGTTCCGGAGGTCCAGGATCTGCAGGGAGCAGTTGAACTTGAGCAGGTTACCCAGCTGGG GTGGTTGTTCCGGAGGTCCAGGATCTGCAGGGGGCAGTTGAACTTGAGCAGGTTACCCAGCTGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45142364..45142514 32194978 MeRIP-seq:(Medium) rs755923478 Functional Loss SNV dbSNP153 33..33 33 - - - 69640 RMVar_ID_69640 Human_SNP_ID_667116321 m1A Human chr19 - 45147173 45147173 45147173 CCCTCACCCACACCCATGCCACTCGCCCCCAAAGGGCTGTAGTGCCTCTCAGGGCGCAGCCTCCA CCCTCACCCACACCCATGCCACTCGCCCCCAACGGGCTGTAGTGCCTCTCAGGGCGCAGCCTCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45147132..45147232 26863196 MeRIP-seq:(Medium) rs544076550 Functional Loss SNV dbSNP153 33..33 33 - - - 69641 RMVar_ID_69641 Human_SNP_ID_667118631 m1A Human chr19 + 45154107 45154107 45154107 AGAGCCAGGGATGGGCAAGAGGCTGGAGGCGGAGCGAGGGTGTGGAGGGCACCGGGAAGGTTCTG AGAGCCAGGGATGGGCAAGAGGCTGGAGGCGGGGCGAGGGTGTGGAGGGCACCGGGAAGGTTCTG A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:45153981..45154195;chr19:45154018..45154153 26863196 MeRIP-seq:(Medium) rs1485506669 Functional Loss SNV dbSNP153 33..33 33 - - - 69642 RMVar_ID_69642 Human_SNP_ID_667121199 m1A Human chr19 - 45163006 45163006 45163006 TCAGAGGAGGCAAAGGGGTCCCAGCTGCGGTCAGGACTGTGGTGGGATTCCCGCCTCGGCAGCGT TCAGAGGAGGCAAAGGGGTCCCAGCTGCGGTCGGGACTGTGGTGGGATTCCCGCCTCGGCAGCGT T C TRAPPC6A Ensembl:ENSG00000007255 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45162960..45163126 26863196 MeRIP-seq:(Medium) rs1021547481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523492,Human_RBP_ID_5145290,Human_RBP_ID_5238819,Human_RBP_ID_26472611 RMVar_hsa_circ_95660,RMVar_hsa_circ_128160,RMVar_hsa_circ_195288,RMVar_hsa_circ_195289 69643 RMVar_ID_69643 Human_SNP_ID_667121286 m1A Human chr19 - 45163220 45163220 45163220 TCAAGCCTAAGCCAGGCCTTCTCTTCCAGGTAAGTTCCAGGTGGTGATTCCGAAATCCTAAGCCT TCAAGCCTAAGCCAGGCCTTCTCTTCCAGGTACGTTCCAGGTGGTGATTCCGAAATCCTAAGCCT T G TRAPPC6A Ensembl:ENSG00000007255 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45163025..45163222 32194978 MeRIP-seq:(Medium) rs572050421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22662821,Human_RBP_ID_23211305 Human_Splice_Rec_2018770,Human_Splice_Rec_2018778,Human_Splice_Rec_2018788,Human_Splice_Rec_2018796 RMVar_hsa_circ_95660,RMVar_hsa_circ_128160,RMVar_hsa_circ_195288,RMVar_hsa_circ_195289 69644 RMVar_ID_69644 Human_SNP_ID_667121659 m1A Human chr19 + 45164201 45164201 45164201 GTGCTTCCTCCAGATACTGCAGGCCAGAGGCCATCGGGAGGAGGAGGGGGAAGCTGTTGTCTTGC GTGCTTCCTCCAGATACTGCAGGCCAGAGGCCGTCGGGAGGAGGAGGGGGAAGCTGTTGTCTTGC A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45163017..45164742 32194978 MeRIP-seq:(Medium) rs201533739 Functional Loss SNV dbSNP153 33..33 33 - - - 69645 RMVar_ID_69645 Human_SNP_ID_667121660 m1A Human chr19 + 45164201 45164201 45164201 GTGCTTCCTCCAGATACTGCAGGCCAGAGGCCATCGGGAGGAGGAGGGGGAAGCTGTTGTCTTGC GTGCTTCCTCCAGATACTGCAGGCCAGAGGCCTTCGGGAGGAGGAGGGGGAAGCTGTTGTCTTGC A T MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45163017..45164742 32194978 MeRIP-seq:(Medium) rs201533739 Functional Loss SNV dbSNP153 33..33 33 - - - 69646 RMVar_ID_69646 Human_SNP_ID_667125658 m1A Human chr19 - 45178185 45178185 45178185 TGGCGGATACTGTGTTGTTTGAGTTTCTTCACACGGAGATGGTGGCTGAGCTGTGGGCTCACGAC TGGCGGATACTGTGTTGTTTGAGTTTCTTCACCCGGAGATGGTGGCTGAGCTGTGGGCTCACGAC T G TRAPPC6A Ensembl:ENSG00000007255 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:45165142..45178225;chr19:45178050..45178219;chr19:45165142..45178208;chr19:45164870..45178205 26863196 MeRIP-seq:(Medium) rs1438026284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4536433,Human_RBP_ID_23210980,Human_RBP_ID_23800986 Human_Splice_Rec_2018761,Human_Splice_Rec_2018771,Human_Splice_Rec_2018779,Human_Splice_Rec_2018789,Human_Splice_Rec_2018797 69647 RMVar_ID_69647 Human_SNP_ID_667125910 m1A Human chr19 - 45178833 45178833 45178833 GGGATGGGAGAAGCGCTAACGCCAAAGACCGTACCCGGCAGCTGACGCTCGGAGCTTGCGAGATC GGGATGGGAGAAGCGCTAACGCCAAAGACCGTTCCCGGCAGCTGACGCTCGGAGCTTGCGAGATC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45178791..45178876 26863196 MeRIP-seq:(Medium) rs1371107831 Functional Loss SNV dbSNP153 33..33 33 - - - 69648 RMVar_ID_69648 Human_SNP_ID_667126059 m1A Human chr19 + 45179321 45179321 45179321 TCGGTGCCATGGCGTCCCAGGGTCGTCGGCGGAGGCCCCTGCGGAGGCCGGAGACGGTGGTGCCG TCGGTGCCATGGCGTCCCAGGGTCGTCGGCGGTGGCCCCTGCGGAGGCCGGAGACGGTGGTGCCG A T MARK4,BLOC1S3 Ensembl:ENSG00000007047,Ensembl:ENSG00000189114 Protein coding,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45179298..45179486 26863196 MeRIP-seq:(Medium) rs769359711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2018802 RMVar_hsa_circ_80475,RMVar_hsa_circ_100453,RMVar_hsa_circ_195291,RMVar_hsa_circ_195292 69649 RMVar_ID_69649 Human_SNP_ID_667126076 m1A Human chr19 - 45179349 45179349 45179349 GCTCGGAATCCGTCTCGGTCGCCTCCCCCGGCACCACCGTCTCCGGCCTCCGCAGGGGCCTCCGC GCTCGGAATCCGTCTCGGTCGCCTCCCCCGGCCCCACCGTCTCCGGCCTCCGCAGGGGCCTCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45179234..45179531 26863196 MeRIP-seq:(Medium) rs1278115093 Functional Loss SNV dbSNP153 33..33 33 - - - 69650 RMVar_ID_69650 Human_SNP_ID_667126112 m1A Human chr19 - 45179390 45179390 45179390 ACCCAGGTACAGCTCCTCCTCCTCCGACGAGGACGCAGAGCGCTCGGAATCCGTCTCGGTCGCCT ACCCAGGTACAGCTCCTCCTCCTCCGACGAGGGCGCAGAGCGCTCGGAATCCGTCTCGGTCGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45179341..45179523 26863196 MeRIP-seq:(Medium) rs1219782141 Functional Loss SNV dbSNP153 33..33 33 - - - 69651 RMVar_ID_69651 Human_SNP_ID_667145783 m1A Human chr19 + 45251369 45251369 45251369 GGCCCCCGCCCGCCCGCCTGCCCGCCGCCCCCATGGCGCCCGGGGTCCCCGCTGCACGGGGCCAC GGCCCCCGCCCGCCCGCCTGCCCGCCGCCCCCCTGGCGCCCGGGGTCCCCGCTGCACGGGGCCAC A C MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45251276..45251616 26863410 MeRIP-seq:(Medium) rs1205084272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558563,Human_RBP_ID_9329014,Human_RBP_ID_26784384 69652 RMVar_ID_69652 Human_SNP_ID_667147184 m1A Human chr19 + 45256506 45256506 45256506 GAGTCCAATCTGGGGTAACAGTGATTGGAATCAAATGTTAGGGGCATTCCACTGGGAATCAAATG GAGTCCAATCTGGGGTAACAGTGATTGGAATCCAATGTTAGGGGCATTCCACTGGGAATCAAATG A C MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45256504..45256644 26863196 MeRIP-seq:(Medium) rs1357785070 Functional Loss SNV dbSNP153 33..33 33 - - - 69653 RMVar_ID_69653 Human_SNP_ID_667147899 m1A Human chr19 - 45259016 45259016 45259016 TGAGCGGCTGGACCAGGACGGGCCTTTGTCCGAGGAGCGGCCACTGCCCAAGGTGCCATGCTGGG TGAGCGGCTGGACCAGGACGGGCCTTTGTCCGGGGAGCGGCCACTGCCCAAGGTGCCATGCTGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45251466..45259018 32194978 MeRIP-seq:(Medium) rs1423133877 Functional Loss SNV dbSNP153 33..33 33 - - - 69654 RMVar_ID_69654 Human_SNP_ID_667149814 m1A Human chr19 + 45265567 45265567 45265567 GTGAGGGTGCCCAGGTATGTGGGATAAGAAGAAGTGCAGGTATAAGGGTGCCCAGGTGTGGGGTA GTGAGGGTGCCCAGGTATGTGGGATAAGAAGATGTGCAGGTATAAGGGTGCCCAGGTGTGGGGTA A T MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45265562..45265796 26863196 MeRIP-seq:(Medium) rs1306144336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93983,RMVar_hsa_circ_288821,RMVar_hsa_circ_322217,RMVar_hsa_circ_313861,RMVar_hsa_circ_195295,RMVar_hsa_circ_195296,RMVar_hsa_circ_345827,RMVar_hsa_circ_282569,RMVar_hsa_circ_267826,RMVar_hsa_circ_195306,RMVar_hsa_circ_114875,RMVar_hsa_circ_104036,RMVar_hsa_circ_195298,RMVar_hsa_circ_195299,RMVar_hsa_circ_195297,RMVar_hsa_circ_264951,RMVar_hsa_circ_195302,RMVar_hsa_circ_272702,RMVar_hsa_circ_88830,RMVar_hsa_circ_93749,RMVar_hsa_circ_195308,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_195307,RMVar_hsa_circ_79500,RMVar_hsa_circ_195304,RMVar_hsa_circ_195305,RMVar_hsa_circ_195310 69655 RMVar_ID_69655 Human_SNP_ID_667153913 m1A Human chr19 - 45280436 45280436 45280436 CAGCAGGAGGTAGGTGGCGGTCACTTCGTTGTACTTCTGGCTGGTCAAGGACTCTTTGATTTCTT CAGCAGGAGGTAGGTGGCGGTCACTTCGTTGTCCTTCTGGCTGGTCAAGGACTCTTTGATTTCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45280385..45280685 26863196 MeRIP-seq:(Medium) rs754653981 Functional Loss SNV dbSNP153 33..33 33 - - - 69656 RMVar_ID_69656 Human_SNP_ID_667155930 m1A Human chr19 + 45287519 45287519 45287519 GACGAGCACGGGGGAGGCGGAGCTGAAGGAGGAGCGGCTGCCAGGCCGGAAGGCGAGCTGCAGCA GACGAGCACGGGGGAGGCGGAGCTGAAGGAGGGGCGGCTGCCAGGCCGGAAGGCGAGCTGCAGCA A G MARK4 Ensembl:ENSG00000007047 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45287418..45287612 26863196 MeRIP-seq:(Medium) rs1265165331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2018584,Human_Splice_Rec_2018616,Human_Splice_Rec_2018678,Human_Splice_Rec_2018688,Human_Splice_Rec_2018692 RMVar_hsa_circ_93983,RMVar_hsa_circ_9377,RMVar_hsa_circ_114875,RMVar_hsa_circ_195297,RMVar_hsa_circ_88830,RMVar_hsa_circ_195308,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_195307,RMVar_hsa_circ_26071,RMVar_hsa_circ_195317,RMVar_hsa_circ_101057,RMVar_hsa_circ_304047,RMVar_hsa_circ_375992,RMVar_hsa_circ_121313,RMVar_hsa_circ_195318,RMVar_hsa_circ_195316,RMVar_hsa_circ_358665,RMVar_hsa_circ_42346 69657 RMVar_ID_69657 Human_SNP_ID_667158571 m1A Human chr19 + 45297727 45297727 45297727 CCCCCTGCCTCCCCCTCCAGTCACAGCCTGGCACCCCCATCAGGGGAGCGGAGCCGCCTGGCACG CCCCCTGCCTCCCCCTCCAGTCACAGCCTGGCGCCCCCATCAGGGGAGCGGAGCCGCCTGGCACG A G MARK4 Ensembl:ENSG00000007047 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45297638..45297762 26863196 MeRIP-seq:(Medium) rs939611678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21892762 Human_Splice_Rec_2018588,Human_Splice_Rec_2018620 RMVar_hsa_circ_93983,RMVar_hsa_circ_195297,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_121313,RMVar_hsa_circ_195318,RMVar_hsa_circ_42346 69658 RMVar_ID_69658 Human_SNP_ID_667158610 m1A Human chr19 - 45297790 45297790 45297790 CCACCCCCTGCCCGCCGGTCCCGGACCTGGCCACCATGGAAGGTGCTGCGGATGGTGGAACCACG CCACCCCCTGCCCGCCGGTCCCGGACCTGGCCGCCATGGAAGGTGCTGCGGATGGTGGAACCACG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45297704..45297805 26863410 MeRIP-seq:(Medium) rs942773837 Functional Loss SNV dbSNP153 33..33 33 - - - 69659 RMVar_ID_69659 Human_SNP_ID_667158611 m1A Human chr19 - 45297790 45297790 45297790 CCACCCCCTGCCCGCCGGTCCCGGACCTGGCCACCATGGAAGGTGCTGCGGATGGTGGAACCACG CCACCCCCTGCCCGCCGGTCCCGGACCTGGCCCCCATGGAAGGTGCTGCGGATGGTGGAACCACG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45297704..45297805 26863410 MeRIP-seq:(Medium) rs942773837 Functional Loss SNV dbSNP153 33..33 33 - - - 69660 RMVar_ID_69660 Human_SNP_ID_667160155 m1A Human chr19 + 45302694 45302694 45302694 GGCCTTCCGCACCCTCGTCACCCGCATCTCCAACGACCTCGAGCTCTGAGCCACCACGGTCCCAG GGCCTTCCGCACCCTCGTCACCCGCATCTCCAGCGACCTCGAGCTCTGAGCCACCACGGTCCCAG A G MARK4 Ensembl:ENSG00000007047 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45302645..45302745 26863196 MeRIP-seq:(Medium) rs756693005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18192308,Human_RBP_ID_27469083 RMVar_hsa_circ_83144,RMVar_hsa_circ_195309 69661 RMVar_ID_69661 Human_SNP_ID_667171894 m1A Human chr19 - 45341752 45341752 45341752 ACACACACGCACACACGGCTTCACACACCTCCACACCTCACTCATCCAACCCCAAGGTTCCACGC ACACACACGCACACACGGCTTCACACACCTCCCCACCTCACTCATCCAACCCCAAGGTTCCACGC T G lnc-ERCC2-1 RNACentral:URS00009C2807 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45341748..45341939 26863196 MeRIP-seq:(Medium) rs932080664 Functional Loss SNV dbSNP153 33..33 33 - - - 69662 RMVar_ID_69662 Human_SNP_ID_667174882 m1A Human chr19 - 45349168 45349168 45349168 GGGCTTGTGCTGGTGGCCATGAGGGGTTGGAAAGGCTATGGGGGGACCCAGTTGGAGGGTGATGT GGGCTTGTGCTGGTGGCCATGAGGGGTTGGAAGGGCTATGGGGGGACCCAGTTGGAGGGTGATGT T C lnc-ERCC2-1 RNACentral:URS00009C2807 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45349120..45349222 26863196 MeRIP-seq:(Medium) rs187603368 Functional Loss SNV dbSNP153 33..33 33 - - - 69663 RMVar_ID_69663 Human_SNP_ID_667175648 m1A Human chr19 - 45350515 45350494 45350516 TCTGCGTCACCAGCTGTGCCTGTGTTGGGGGCACCTAGGGGGAAAGATGGGGGACACTGAGATGG TCTGCGTCACCAGCTGTGCCTGTGTTGGGGG______________________ACACTGAGATGG TCCCCCATCTTTCCCCCTAGGTG T ERCC2 Ensembl:ENSG00000104884 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:45350469..45350607;chr19:45350469..45350755 26863196 MeRIP-seq:(Medium) rs752441115 Functional Loss DEL dbSNP153 32..53 33 - - - Human_RBP_ID_5116314,Human_RBP_ID_22070297,Human_RBP_ID_22665579,Human_RBP_ID_26472619 69664 RMVar_ID_69664 Human_SNP_ID_667175652 m1A Human chr19 - 45350515 45350495 45350516 TCTGCGTCACCAGCTGTGCCTGTGTTGGGGGCACCTAGGGGGAAAGATGGGGGACACTGAGATGG TCTGCGTCACCAGCTGTGCCTGTGTTGGGGG_____________________GACACTGAGATGG CCCCCATCTTTCCCCCTAGGTG C ERCC2 Ensembl:ENSG00000104884 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:45350469..45350607;chr19:45350469..45350755 26863196 MeRIP-seq:(Medium) rs763627642 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_5116314,Human_RBP_ID_22070297,Human_RBP_ID_22665579,Human_RBP_ID_26472619 69665 RMVar_ID_69665 Human_SNP_ID_667176939 m1A Human chr19 - 45352306 45352306 45352306 GGACAAGCGGGGGAAGCTGCCCCGCTGGATCCAGGAGCACCTCACAGATGCCAACCTCAACCTGA GGACAAGCGGGGGAAGCTGCCCCGCTGGATCCCGGAGCACCTCACAGATGCCAACCTCAACCTGA T G ERCC2 Ensembl:ENSG00000104884 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45351636..45352350 32194978 MeRIP-seq:(Medium) rs999070778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22977769 Human_Splice_Rec_2019008,Human_Splice_Rec_2019009,Human_Splice_Rec_2019050,Human_Splice_Rec_2019051,Human_Splice_Rec_2019090,Human_Splice_Rec_2019091,Human_Splice_Rec_2019108,Human_Splice_Rec_2019109,Human_Splice_Rec_2019130,Human_Splice_Rec_2019131,Human_Splice_Rec_2019172 Human_miRNA_ID_2007825,Human_miRNA_ID_2673463 RMVar_hsa_circ_195321,RMVar_hsa_circ_105895 69666 RMVar_ID_69666 Human_SNP_ID_667178410 m1A Human chr19 - 45355725 45355725 45355725 CGCTTATCGTGACCTCTGTTGCTCTCCAGATCATCGGCCGTGGCAATGACCAGGTGGCCATCAGC CGCTTATCGTGACCTCTGTTGCTCTCCAGATCGTCGGCCGTGGCAATGACCAGGTGGCCATCAGC T C ERCC2 Ensembl:ENSG00000104884 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45355651..45355725 32194978 MeRIP-seq:(Medium) rs370293513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4536644,Human_RBP_ID_6773468,Human_RBP_ID_13475166 Human_Splice_Rec_2018996,Human_Splice_Rec_2018997,Human_Splice_Rec_2019038,Human_Splice_Rec_2019039,Human_Splice_Rec_2019078,Human_Splice_Rec_2019079,Human_Splice_Rec_2019096,Human_Splice_Rec_2019097,Human_Splice_Rec_2019118,Human_Splice_Rec_2019119,Human_Splice_Rec_2019160,Human_Splice_Rec_2019161 Human_miRNA_ID_2939101 RMVar_hsa_circ_82310,RMVar_hsa_circ_195321,RMVar_hsa_circ_105895,RMVar_hsa_circ_100054,RMVar_hsa_circ_195324,RMVar_hsa_circ_108548,RMVar_hsa_circ_195322,RMVar_hsa_circ_195323,RMVar_hsa_circ_372930,RMVar_hsa_circ_195325,RMVar_hsa_circ_195326,RMVar_hsa_circ_292276 69667 RMVar_ID_69667 Human_SNP_ID_667179112 m1A Human chr19 + 45357696 45357696 45357696 TTCTGTCGTCAAAGGGCTCGATGATGATGGTGAAGCCTGCAGAGGGCAGGCAAGGAGGGGTGAGA TTCTGTCGTCAAAGGGCTCGATGATGATGGTGGAGCCTGCAGAGGGCAGGCAAGGAGGGGTGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45357694..45358011 26863196 MeRIP-seq:(Medium) rs1354803589 Functional Loss SNV dbSNP153 33..33 33 - - - 69668 RMVar_ID_69668 Human_SNP_ID_667179725 m1A Human chr19 + 45359228 45359228 45359228 AGGATGAGGGGGAGGTGGTTGGGGGATGAGGAAGATGAGGAAGGATGATCCAGGTGAAAGACCAT AGGATGAGGGGGAGGTGGTTGGGGGATGAGGAGGATGAGGAAGGATGATCCAGGTGAAAGACCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45359215..45359373 26863196 MeRIP-seq:(Medium) rs998502466 Functional Loss SNV dbSNP153 33..33 33 - - - 69669 RMVar_ID_69669 Human_SNP_ID_667179874 m1A Human chr19 - 45359715 45359715 45359715 TGGGTGGCAGGCAGGGACCTGAGCAGGAGGGGAGGGGCCTTGGCCAGGATGTGGCCATGGGGAGA TGGGTGGCAGGCAGGGACCTGAGCAGGAGGGGGGGGGCCTTGGCCAGGATGTGGCCATGGGGAGA T C ERCC2 Ensembl:ENSG00000104884 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45359547..45359854 26863196 MeRIP-seq:(Medium) rs1297475035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359054 RMVar_hsa_circ_82310,RMVar_hsa_circ_100054,RMVar_hsa_circ_108548,RMVar_hsa_circ_195322,RMVar_hsa_circ_195323,RMVar_hsa_circ_195325,RMVar_hsa_circ_195328,RMVar_hsa_circ_319627 69670 RMVar_ID_69670 Human_SNP_ID_667181236 m1A Human chr19 - 45363821 45363821 45363821 GCTGGAGTACGTGAAGTGGCGGCTGCGTGTGCAGCATGTGGTGCAGGAGAGCCCGCCCGCCTTCC GCTGGAGTACGTGAAGTGGCGGCTGCGTGTGCGGCATGTGGTGCAGGAGAGCCCGCCCGCCTTCC T C ERCC2 Ensembl:ENSG00000104884 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45363770..45363995 32194978 MeRIP-seq:(Medium) rs1270366302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955186,Human_RBP_ID_9293802,Human_RBP_ID_18998128 Human_Splice_Rec_2018986,Human_Splice_Rec_2018987,Human_Splice_Rec_2019028,Human_Splice_Rec_2019029,Human_Splice_Rec_2019068,Human_Splice_Rec_2019069,Human_Splice_Rec_2019150,Human_Splice_Rec_2019151,Human_Splice_Rec_2019174,Human_Splice_Rec_2019175,Human_Splice_Rec_2019206,Human_Splice_Rec_2019207 RMVar_hsa_circ_114863,RMVar_hsa_circ_82310,RMVar_hsa_circ_100054,RMVar_hsa_circ_108548,RMVar_hsa_circ_195322,RMVar_hsa_circ_195323,RMVar_hsa_circ_195325,RMVar_hsa_circ_370228,RMVar_hsa_circ_21071,RMVar_hsa_circ_48639,RMVar_hsa_circ_103606,RMVar_hsa_circ_33359,RMVar_hsa_circ_35461,RMVar_hsa_circ_195331,RMVar_hsa_circ_14987,RMVar_hsa_circ_195332,RMVar_hsa_circ_195330,RMVar_hsa_circ_67133 69671 RMVar_ID_69671 Human_SNP_ID_667182982 m1A Human chr19 - 45368726 45368726 45368726 CCAACTTTGGAGTAGGTGATTGAAGAGCTTCGAAAGTTGCTCAACTTCTATGAGAAGCAGGAGGG CCAACTTTGGAGTAGGTGATTGAAGAGCTTCGCAAGTTGCTCAACTTCTATGAGAAGCAGGAGGG T G ERCC2 Ensembl:ENSG00000104884 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45368676..45368750 32194978 MeRIP-seq:(Medium) rs1236941342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18995125 Human_Splice_Rec_2018974,Human_Splice_Rec_2018975,Human_Splice_Rec_2019016,Human_Splice_Rec_2019017,Human_Splice_Rec_2019060,Human_Splice_Rec_2019061,Human_Splice_Rec_2019138,Human_Splice_Rec_2019139,Human_Splice_Rec_2019194,Human_Splice_Rec_2019195,Human_Splice_Rec_2019218,Human_Splice_Rec_2019219,Human_Splice_Rec_2019236,Human_Splice_Rec_2019237,Human_Splice_Rec_2019244,Human_Splice_Rec_2019245,Human_Splice_Rec_2019252,Human_Splice_Rec_2019253,Human_Splice_Rec_2019262,Human_Splice_Rec_2019263 Human_miRNA_ID_2536800 RMVar_hsa_circ_100054,RMVar_hsa_circ_108548,RMVar_hsa_circ_195322,RMVar_hsa_circ_195325,RMVar_hsa_circ_21071,RMVar_hsa_circ_103606,RMVar_hsa_circ_33359,RMVar_hsa_circ_35461,RMVar_hsa_circ_195332,RMVar_hsa_circ_83418,RMVar_hsa_circ_322690,RMVar_hsa_circ_296490,RMVar_hsa_circ_195334,RMVar_hsa_circ_195335 69672 RMVar_ID_69672 Human_SNP_ID_667183483 m1A Human chr19 - 45370264 45370264 45370264 GGCACTGTGGAGGCGGGAGAGGGGCTGAGGGGACGGGAACTGACCCAGCAGCCCCTGCCGCCAGG GGCACTGTGGAGGCGGGAGAGGGGCTGAGGGGGCGGGAACTGACCCAGCAGCCCCTGCCGCCAGG T C ERCC2 Ensembl:ENSG00000104884 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45370258..45370538 26863196 MeRIP-seq:(Medium) rs1239184034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239497,Human_RBP_ID_770535,Human_RBP_ID_825352,Human_RBP_ID_22546133,Human_RBP_ID_22663960 Human_miRNA_ID_1967504,Human_miRNA_ID_2245863 RMVar_hsa_circ_100320,RMVar_hsa_circ_195336 69673 RMVar_ID_69673 Human_SNP_ID_667187081 m1A Human chr19 - 45382594 45382594 45382594 GTCGGTCACCGTGCTGCGGAGGGACGGGCCGGAGGAGACCGACTGGTGGTGGGCCGCGCTGCACG GTCGGTCACCGTGCTGCGGAGGGACGGGCCGGTGGAGACCGACTGGTGGTGGGCCGCGCTGCACG T A PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:45382551..45385564;chr19:45382352..45382662 26863196 MeRIP-seq:(Medium) rs1223577772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523597 Human_Splice_Rec_2019265,Human_Splice_Rec_2019277,Human_Splice_Rec_2019301,Human_Splice_Rec_2019325 RMVar_hsa_circ_12194,RMVar_hsa_circ_354819 69674 RMVar_ID_69674 Human_SNP_ID_667187110 m1A Human chr19 - 45382633 45382633 45382633 CGCCGAGTTCGGGGACGAGCTGTCCTTCCGCGAGGGCGAGTCGGTCACCGTGCTGCGGAGGGACG CGCCGAGTTCGGGGACGAGCTGTCCTTCCGCGTGGGCGAGTCGGTCACCGTGCTGCGGAGGGACG T A PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45382586..45382677 26863196 MeRIP-seq:(Medium) rs1326364229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2019276,Human_Splice_Rec_2019300,Human_Splice_Rec_2019324,Human_Splice_Rec_2019330 RMVar_hsa_circ_12194,RMVar_hsa_circ_354819 69675 RMVar_ID_69675 Human_SNP_ID_667191643 m1A Human chr19 - 45396880 45396880 45396880 GGGACGGCCGTCGTCGCCGCGCACCCCGCTCTACCTGCAGCCGGACGCCTACGGCAGCCTGGACC GGGACGGCCGTCGTCGCCGCGCACCCCGCTCTGCCTGCAGCCGGACGCCTACGGCAGCCTGGACC T C PPP1R13L Ensembl:ENSG00000104881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45396580..45397046 26863196 MeRIP-seq:(Medium) rs1314781590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 69676 RMVar_ID_69676 Human_SNP_ID_667191684 m1A Human chr19 - 45396939 45396939 45396939 CCGTTCGGACGATCAGAGAGTGCCCCAACCCTACACCCCTACAGCCCGCTGTCCCCCAAGGGACG CCGTTCGGACGATCAGAGAGTGCCCCAACCCTTCACCCCTACAGCCCGCTGTCCCCCAAGGGACG T A PPP1R13L Ensembl:ENSG00000104881 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45396647..45397075 26863196 MeRIP-seq:(Medium) rs1183684624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 69677 RMVar_ID_69677 Human_SNP_ID_667192157 m1A Human chr19 - 45398126 45398126 45398126 CACCTTCCCAGCGCTGGCCATGAAACACATGGATCTGAAGCAGATGGAGCTGGACACGGCGGCGG CACCTTCCCAGCGCTGGCCATGAAACACATGGTTCTGAAGCAGATGGAGCTGGACACGGCGGCGG T A PPP1R13L Ensembl:ENSG00000104881 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45397915..45398150 26863196 MeRIP-seq:(Medium) rs1021112589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957124,Human_RBP_ID_18998144,Human_RBP_ID_26337981,Human_RBP_ID_27816534 Human_Splice_Rec_2019282,Human_Splice_Rec_2019306,Human_Splice_Rec_2019334,Human_Splice_Rec_2019348,Human_Splice_Rec_2019356 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339,RMVar_hsa_circ_195341,RMVar_hsa_circ_271076 69678 RMVar_ID_69678 Human_SNP_ID_667192159 m1A Human chr19 + 45398129 45398129 45398129 CCGCCGTGTCCAGCTCCATCTGCTTCAGATCCATGTGTTTCATGGCCAGCGCTGGGAAGGTGGGA CCGCCGTGTCCAGCTCCATCTGCTTCAGATCCTTGTGTTTCATGGCCAGCGCTGGGAAGGTGGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45397960..45398350 26863196 MeRIP-seq:(Medium) rs781303663 Functional Loss SNV dbSNP153 33..33 33 - - - 69679 RMVar_ID_69679 Human_SNP_ID_667192250 m1A Human chr19 - 45398304 45398304 45398304 CCCGCTCCGGCCGGCACCATGGACAGCGAGGCATTCCAGAGCGCGCGGGACTTTCTGGACATGAA CCCGCTCCGGCCGGCACCATGGACAGCGAGGCGTTCCAGAGCGCGCGGGACTTTCTGGACATGAA T C PPP1R13L Ensembl:ENSG00000104881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45398140..45402016 26863196 MeRIP-seq:(Medium) rs781050699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17927837 Human_Splice_Rec_2019280,Human_Splice_Rec_2019281,Human_Splice_Rec_2019304,Human_Splice_Rec_2019305,Human_Splice_Rec_2019332,Human_Splice_Rec_2019333,Human_Splice_Rec_2019346,Human_Splice_Rec_2019347,Human_Splice_Rec_2019354,Human_Splice_Rec_2019355 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339,RMVar_hsa_circ_195341,RMVar_hsa_circ_271076 69680 RMVar_ID_69680 Human_SNP_ID_667193586 m1A Human chr19 - 45402683 45402682 45402683 AGCACATGGGAGAGGACTCGGAGGCAGAGGTCAGGGGCAGAGGCCTGGGAACAGACACACGGCCC AGCACATGGGAGAGGACTCGGAGGCAGAGGTC_GGGGCAGAGGCCTGGGAACAGACACACGGCCC CT C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45402675..45402814 26863196 MeRIP-seq:(Medium) rs1481753665 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 69681 RMVar_ID_69681 Human_SNP_ID_667193591 m1A Human chr19 + 45402709 45402709 45402709 TGCCCCTGACCTCTGCCTCCGAGTCCTCTCCCATGTGCTCCCCTCTAGCTCTAGCTCCGAGCTCT TGCCCCTGACCTCTGCCTCCGAGTCCTCTCCCGTGTGCTCCCCTCTAGCTCTAGCTCCGAGCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45402706..45402807 26863196 MeRIP-seq:(Medium) rs911356364 Functional Loss SNV dbSNP153 33..33 33 - - - 69682 RMVar_ID_69682 Human_SNP_ID_667193592 m1A Human chr19 + 45402709 45402709 45402709 TGCCCCTGACCTCTGCCTCCGAGTCCTCTCCCATGTGCTCCCCTCTAGCTCTAGCTCCGAGCTCT TGCCCCTGACCTCTGCCTCCGAGTCCTCTCCCTTGTGCTCCCCTCTAGCTCTAGCTCCGAGCTCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45402706..45402807 26863196 MeRIP-seq:(Medium) rs911356364 Functional Loss SNV dbSNP153 33..33 33 - - - 69683 RMVar_ID_69683 Human_SNP_ID_667195221 m1A Human chr19 + 45408624 45408624 45408624 GGATGTGCGGAAGAAGAAGAAGAAAAAAAATCAGCAGCTGAAAGAACCAGAGGCAGCAGGGCCTG GGATGTGCGGAAGAAGAAGAAGAAAAAAAATCCGCAGCTGAAAGAACCAGAGGCAGCAGGGCCTG A C CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45408494..45408712 26863196 MeRIP-seq:(Medium) rs778011053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1568309 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 69684 RMVar_ID_69684 Human_SNP_ID_667195222 m1A Human chr19 + 45408624 45408624 45408624 GGATGTGCGGAAGAAGAAGAAGAAAAAAAATCAGCAGCTGAAAGAACCAGAGGCAGCAGGGCCTG GGATGTGCGGAAGAAGAAGAAGAAAAAAAATCGGCAGCTGAAAGAACCAGAGGCAGCAGGGCCTG A G CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45408494..45408712 26863196 MeRIP-seq:(Medium) rs778011053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1568309 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 69685 RMVar_ID_69685 Human_SNP_ID_667195485 m1A Human chr19 + 45409233 45409233 45409233 CCTTGAGCCTCAGGCAGCTCCCACATCCACCAAGAAGAAGAAGAAGAAGAAAGAGAGAGGTCACA CCTTGAGCCTCAGGCAGCTCCCACATCCACCACGAAGAAGAAGAAGAAGAAAGAGAGAGGTCACA A C CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45409182..45409282 32194978 MeRIP-seq:(Medium) rs773205526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53484,Human_RBP_ID_914969,Human_RBP_ID_17936509,Human_RBP_ID_26336413 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 69686 RMVar_ID_69686 Human_SNP_ID_667195555 m1A Human chr19 + 45409402 45409402 45409402 CAGGAAAGCCGGATGCCAGAGACAGTGCCCCAAGAGGAGATGCCAGGGCCGCCACTGAATTCAGA CAGGAAAGCCGGATGCCAGAGACAGTGCCCCAGGAGGAGATGCCAGGGCCGCCACTGAATTCAGA A G CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45409219..45409483 26863196 MeRIP-seq:(Medium) rs964169447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359056,Human_RBP_ID_26336414 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 69687 RMVar_ID_69687 Human_SNP_ID_667195703 m1A Human chr19 - 45409709 45409709 45409709 TCTCCCTCCCATCCAGGCCCGGAGGCTGTTTGATGTCCTGCACGAGCCCTTCTTGAAAGTACCCT TCTCCCTCCCATCCAGGCCCGGAGGCTGTTTGGTGTCCTGCACGAGCCCTTCTTGAAAGTACCCT T C ERCC1 Ensembl:ENSG00000012061 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:45409529..45409826;chr19:45407148..45409777 32194978 MeRIP-seq:(Medium) rs1294107546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2019386,Human_Splice_Rec_2019402,Human_Splice_Rec_2019408,Human_Splice_Rec_2019424,Human_Splice_Rec_2019430,Human_Splice_Rec_2019440,Human_Splice_Rec_2019458 RMVar_hsa_circ_122862,RMVar_hsa_circ_378421,RMVar_hsa_circ_195345,RMVar_hsa_circ_94010,RMVar_hsa_circ_101592,RMVar_hsa_circ_195347,RMVar_hsa_circ_77741,RMVar_hsa_circ_195346,RMVar_hsa_circ_195343,RMVar_hsa_circ_195344 69688 RMVar_ID_69688 Human_SNP_ID_667199368 m1A Human chr19 + 45422053 45422053 45422053 CTCCCCCACTCCTCAGCCTCCACTCTGGTCCCAGCCACCAGCGTTTCACCCTTGGACCACTGAAG CTCCCCCACTCCTCAGCCTCCACTCTGGTCCCGGCCACCAGCGTTTCACCCTTGGACCACTGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45422052..45422399 26863196 MeRIP-seq:(Medium) rs1041944872 Functional Loss SNV dbSNP153 33..33 33 - - - 69689 RMVar_ID_69689 Human_SNP_ID_667199825 m1A Human chr19 - 45423782 45423782 45423782 TCGCGGCGCTGAAACCGTGAGGCCCGGACCACAGGTGCGGGAGGCGGAGACTGCGGGTGGAGATT TCGCGGCGCTGAAACCGTGAGGCCCGGACCACCGGTGCGGGAGGCGGAGACTGCGGGTGGAGATT T G ERCC1 Ensembl:ENSG00000012061 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45423764..45423850 26863196 MeRIP-seq:(Medium) rs1274175360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4536846,Human_RBP_ID_19090408 Human_Splice_Rec_2019369,Human_Splice_Rec_2019409 RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 69690 RMVar_ID_69690 Human_SNP_ID_667205256 m1A Human chr19 - 45443837 45443837 45443837 CCGGTTCGGAGAAAGAACCGAACTGCAGGGCCACAGGAGGGTAGAGTTGGGAGGAGATAGGATCC CCGGTTCGGAGAAAGAACCGAACTGCAGGGCCGCAGGAGGGTAGAGTTGGGAGGAGATAGGATCC T C ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45443830..45443983 26863196 MeRIP-seq:(Medium) rs1177022589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 69691 RMVar_ID_69691 Human_SNP_ID_667214935 m1A Human chr19 - 45478617 45478617 45478617 AACCTGTAGCTGTCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGGTAGTAACTAAGCGCC AACCTGTAGCTGTCTAGCGACAGAGTGGTTCATTTCCACCTTTCGGGCGGTAGTAACTAAGCGCC T A ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs111386994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7748,Human_RBP_ID_239023,Human_RBP_ID_270107,Human_RBP_ID_523637,Human_RBP_ID_1133471,Human_RBP_ID_1190640,Human_RBP_ID_1295015,Human_RBP_ID_1373764,Human_RBP_ID_1568313,Human_RBP_ID_1890082,Human_RBP_ID_2567342,Human_RBP_ID_3573811,Human_RBP_ID_4536879,Human_RBP_ID_5145298,Human_RBP_ID_5190724,Human_RBP_ID_5238821,Human_RBP_ID_5275323,Human_RBP_ID_5421647,Human_RBP_ID_5468928,Human_RBP_ID_5499779,Human_RBP_ID_5641073,Human_RBP_ID_6773587,Human_RBP_ID_8256218,Human_RBP_ID_8490195,Human_RBP_ID_8728084,Human_RBP_ID_8835465,Human_RBP_ID_9088798,Human_RBP_ID_9292466,Human_RBP_ID_9329027,Human_RBP_ID_9341102,Human_RBP_ID_13475392,Human_RBP_ID_17068374,Human_RBP_ID_17084371,Human_RBP_ID_17131947,Human_RBP_ID_17927876,Human_RBP_ID_18179875,Human_RBP_ID_18208434,Human_RBP_ID_18441635,Human_RBP_ID_18514969,Human_RBP_ID_18532560,Human_RBP_ID_18735805,Human_RBP_ID_18947483,Human_RBP_ID_20404038,Human_RBP_ID_21892296,Human_RBP_ID_21908725,Human_RBP_ID_22005467,Human_RBP_ID_22067440,Human_RBP_ID_22236292,Human_RBP_ID_22391290,Human_RBP_ID_22546138,Human_RBP_ID_22592120,Human_RBP_ID_22742533,Human_RBP_ID_22763045,Human_RBP_ID_22811245,Human_RBP_ID_23131472,Human_RBP_ID_23279446,Human_RBP_ID_23801248,Human_RBP_ID_24374707,Human_RBP_ID_24418805,Human_RBP_ID_24484510,Human_RBP_ID_24533195,Human_RBP_ID_24559934,Human_RBP_ID_26749637,Human_RBP_ID_26760159,Human_RBP_ID_26769840,Human_RBP_ID_26991727,Human_RBP_ID_27157685,Human_RBP_ID_27275701,Human_RBP_ID_27469116 RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 69692 RMVar_ID_69692 Human_SNP_ID_667214952 m1A Human chr19 - 45478634 45478634 45478634 CTGGGGTGCAGGCTTCAAACCTGTAGCTGTCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGC CTGGGGTGCAGGCTTCAAACCTGTAGCTGTCTTGCGACAGAGTGGTTCAATTCCACCTTTCGGGC T A ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45478584..45478741 26863196 MeRIP-seq:(Medium) rs188137030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7749,Human_RBP_ID_52403,Human_RBP_ID_239023,Human_RBP_ID_270019,Human_RBP_ID_523638,Human_RBP_ID_1190641,Human_RBP_ID_1568313,Human_RBP_ID_1890083,Human_RBP_ID_3573812,Human_RBP_ID_4536879,Human_RBP_ID_5099562,Human_RBP_ID_5145298,Human_RBP_ID_5193242,Human_RBP_ID_5238822,Human_RBP_ID_5261599,Human_RBP_ID_5275324,Human_RBP_ID_5499780,Human_RBP_ID_5588266,Human_RBP_ID_6773589,Human_RBP_ID_8490198,Human_RBP_ID_8728084,Human_RBP_ID_9088798,Human_RBP_ID_9329027,Human_RBP_ID_9929947,Human_RBP_ID_13475393,Human_RBP_ID_17084371,Human_RBP_ID_17131948,Human_RBP_ID_17269955,Human_RBP_ID_17502767,Human_RBP_ID_17696038,Human_RBP_ID_17936096,Human_RBP_ID_18200702,Human_RBP_ID_18208435,Human_RBP_ID_18306305,Human_RBP_ID_18409459,Human_RBP_ID_18735806,Human_RBP_ID_19096816,Human_RBP_ID_20349506,Human_RBP_ID_21892297,Human_RBP_ID_21908725,Human_RBP_ID_22391290,Human_RBP_ID_22546138,Human_RBP_ID_22592120,Human_RBP_ID_22720539,Human_RBP_ID_22763046,Human_RBP_ID_22811245,Human_RBP_ID_23131472,Human_RBP_ID_23279693,Human_RBP_ID_23309760,Human_RBP_ID_23801249,Human_RBP_ID_24418805,Human_RBP_ID_24484510,Human_RBP_ID_24532643,Human_RBP_ID_24559934,Human_RBP_ID_25425100,Human_RBP_ID_26749637,Human_RBP_ID_26769841,Human_RBP_ID_26991727,Human_RBP_ID_27157686,Human_RBP_ID_27275701,Human_RBP_ID_27469118 RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 69693 RMVar_ID_69693 Human_SNP_ID_667214953 m1A Human chr19 - 45478634 45478634 45478634 CTGGGGTGCAGGCTTCAAACCTGTAGCTGTCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGC CTGGGGTGCAGGCTTCAAACCTGTAGCTGTCTGGCGACAGAGTGGTTCAATTCCACCTTTCGGGC T C ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45478584..45478741 26863196 MeRIP-seq:(Medium) rs188137030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7749,Human_RBP_ID_52403,Human_RBP_ID_239023,Human_RBP_ID_270019,Human_RBP_ID_523638,Human_RBP_ID_1190641,Human_RBP_ID_1568313,Human_RBP_ID_1890083,Human_RBP_ID_3573812,Human_RBP_ID_4536879,Human_RBP_ID_5099562,Human_RBP_ID_5145298,Human_RBP_ID_5193242,Human_RBP_ID_5238822,Human_RBP_ID_5261599,Human_RBP_ID_5275324,Human_RBP_ID_5499780,Human_RBP_ID_5588266,Human_RBP_ID_6773589,Human_RBP_ID_8490198,Human_RBP_ID_8728084,Human_RBP_ID_9088798,Human_RBP_ID_9329027,Human_RBP_ID_9929947,Human_RBP_ID_13475393,Human_RBP_ID_17084371,Human_RBP_ID_17131948,Human_RBP_ID_17269955,Human_RBP_ID_17502767,Human_RBP_ID_17696038,Human_RBP_ID_17936096,Human_RBP_ID_18200702,Human_RBP_ID_18208435,Human_RBP_ID_18306305,Human_RBP_ID_18409459,Human_RBP_ID_18735806,Human_RBP_ID_19096816,Human_RBP_ID_20349506,Human_RBP_ID_21892297,Human_RBP_ID_21908725,Human_RBP_ID_22391290,Human_RBP_ID_22546138,Human_RBP_ID_22592120,Human_RBP_ID_22720539,Human_RBP_ID_22763046,Human_RBP_ID_22811245,Human_RBP_ID_23131472,Human_RBP_ID_23279693,Human_RBP_ID_23309760,Human_RBP_ID_23801249,Human_RBP_ID_24418805,Human_RBP_ID_24484510,Human_RBP_ID_24532643,Human_RBP_ID_24559934,Human_RBP_ID_25425100,Human_RBP_ID_26749637,Human_RBP_ID_26769841,Human_RBP_ID_26991727,Human_RBP_ID_27157686,Human_RBP_ID_27275701,Human_RBP_ID_27469118 RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 69694 RMVar_ID_69694 Human_SNP_ID_667214970 m1A Human chr19 + 45478653 45478653 45478653 ACCACTCTGTCGCTAGACAGCTACAGGTTTGAAGCCTGCACCCCAGACCACTGAGGATCATCCGG ACCACTCTGTCGCTAGACAGCTACAGGTTTGAGGCCTGCACCCCAGACCACTGAGGATCATCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45478584..45478655 26863196 MeRIP-seq:(Medium) rs779958458 Functional Loss SNV dbSNP153 33..33 33 - - - 69695 RMVar_ID_69695 Human_SNP_ID_667214971 m1A Human chr19 + 45478653 45478653 45478653 ACCACTCTGTCGCTAGACAGCTACAGGTTTGAAGCCTGCACCCCAGACCACTGAGGATCATCCGG ACCACTCTGTCGCTAGACAGCTACAGGTTTGATGCCTGCACCCCAGACCACTGAGGATCATCCGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45478584..45478655 26863196 MeRIP-seq:(Medium) rs779958458 Functional Loss SNV dbSNP153 33..33 33 - - - 69696 RMVar_ID_69696 Human_SNP_ID_667218050 m1A Human chr19 + 45488978 45488978 45488978 TCTGCTCCCGAGTCAGGGTGAGGTCCACATCCAGGTAGGCCCTGCGGGGACAAAGGAGTGTGGGG TCTGCTCCCGAGTCAGGGTGAGGTCCACATCCTGGTAGGCCCTGCGGGGACAAAGGAGTGTGGGG A T PPM1N Ensembl:ENSG00000213889 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45488786..45489477 32194978 MeRIP-seq:(Medium) rs1437493801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2019759 69697 RMVar_ID_69697 Human_SNP_ID_667220508 m1A Human chr19 + 45496962 45496960 45496963 ATTCTCGCCGCCTCCTCCTCCCGGGCTGCTCCAGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGC ATTCTCGCCGCCTCCTCCTCCCGGGCTGCTC___CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGC CCAG C PPM1N Ensembl:ENSG00000213889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:45496807..45497001;chr19:45496768..45497031;chr19:45496799..45496991 26863196 MeRIP-seq:(Medium) rs1302412391 Functional Loss DEL dbSNP153 32..34 33 - - - 69698 RMVar_ID_69698 Human_SNP_ID_667220671 m1A Human chr19 + 45497308 45497308 45497308 CTGGCGAGGGACTTGGGAGAGGATGGTGAACGAGCCACGGCAGAGAGGATGAGAGCGTGGATCCC CTGGCGAGGGACTTGGGAGAGGATGGTGAACGCGCCACGGCAGAGAGGATGAGAGCGTGGATCCC A C PPM1N Ensembl:ENSG00000213889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45497227..45497498 26863196 MeRIP-seq:(Medium) rs1163966771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2019767,Human_Splice_Rec_2019773 69699 RMVar_ID_69699 Human_SNP_ID_667221583 m1A Human chr19 - 45499560 45499560 45499560 TCAGGCTCCGCCCCTGTATTTTGGCCCTGCCCACTTCAGGCCACGCCCTTCGCTTGAGTCCTATC TCAGGCTCCGCCCCTGTATTTTGGCCCTGCCCTCTTCAGGCCACGCCCTTCGCTTGAGTCCTATC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45499544..45499753 26863196 MeRIP-seq:(Medium) rs956335952 Functional Loss SNV dbSNP153 33..33 33 - - - 69700 RMVar_ID_69700 Human_SNP_ID_667223652 m1A Human chr19 - 45506724 45506724 45506724 CACGCCCCGCTCTGACTCAGTTTCGCCTGCGGAGGACAGCAGGATCATCCCAGCCCTCAGGAGGG CACGCCCCGCTCTGACTCAGTTTCGCCTGCGGGGGACAGCAGGATCATCCCAGCCCTCAGGAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45506675..45506762 26863196 MeRIP-seq:(Medium) rs1302612783 Functional Loss SNV dbSNP153 33..33 33 - - - 69701 RMVar_ID_69701 Human_SNP_ID_667223921 m1A Human chr19 - 45507527 45507527 45507527 GCAGCAGAAAGGGGATGCAGCGTCCGCTCCCCAGCGCGCACCCCTTGCCGGTGGCGGCTACAGTG GCAGCAGAAAGGGGATGCAGCGTCCGCTCCCCGGCGCGCACCCCTTGCCGGTGGCGGCTACAGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45507476..45507650 26863196 MeRIP-seq:(Medium) rs571898407 Functional Loss SNV dbSNP153 33..33 33 - - - 69702 RMVar_ID_69702 Human_SNP_ID_667223926 m1A Human chr19 - 45507541 45507541 45507541 GATGAGAGGTTCCTGCAGCAGAAAGGGGATGCAGCGTCCGCTCCCCAGCGCGCACCCCTTGCCGG GATGAGAGGTTCCTGCAGCAGAAAGGGGATGCGGCGTCCGCTCCCCAGCGCGCACCCCTTGCCGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:45507476..45507800 26863196 MeRIP-seq:(Medium) rs774158860 Functional Loss SNV dbSNP153 33..33 33 - - - 69703 RMVar_ID_69703 Human_SNP_ID_667227922 m1A Human chr19 + 45521400 45521400 45521400 GAACGGCCCCTCCCCGGAGGAGGTGGAGCAGCAGAAAAGGTGGGGCTGGGCCCTGGGTGGGGAAC GAACGGCCCCTCCCCGGAGGAGGTGGAGCAGCGGAAAAGGTGGGGCTGGGCCCTGGGTGGGGAAC A G VASP Ensembl:ENSG00000125753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45521349..45522381 32194978 MeRIP-seq:(Medium) rs1257769739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26785806 Human_Splice_Rec_2019824,Human_Splice_Rec_2019825 RMVar_hsa_circ_23226,RMVar_hsa_circ_37509,RMVar_hsa_circ_110679,RMVar_hsa_circ_358294,RMVar_hsa_circ_195364,RMVar_hsa_circ_59314,RMVar_hsa_circ_47075,RMVar_hsa_circ_89833,RMVar_hsa_circ_290401,RMVar_hsa_circ_195366,RMVar_hsa_circ_195367 69704 RMVar_ID_69704 Human_SNP_ID_667228725 m1A Human chr19 + 45523693 45523693 45523693 TTGGGGAGAAAACCCCCAAGGATGAATCTGCCAATGTAAGTCAGGGACTCTTCTTGCCCTACATC TTGGGGAGAAAACCCCCAAGGATGAATCTGCCCATGTAAGTCAGGGACTCTTCTTGCCCTACATC A C VASP Ensembl:ENSG00000125753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45522528..45523736 32194978 MeRIP-seq:(Medium) rs761142228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371912,Human_RBP_ID_9346766,Human_RBP_ID_18998154,Human_RBP_ID_19093683,Human_RBP_ID_22665595 Human_Splice_Rec_2019832,Human_Splice_Rec_2019833,Human_Splice_Rec_2019858,Human_Splice_Rec_2019859,Human_Splice_Rec_2019878,Human_Splice_Rec_2019879,Human_Splice_Rec_2019892,Human_Splice_Rec_2019894,Human_Splice_Rec_2019895 RMVar_hsa_circ_37509,RMVar_hsa_circ_110679,RMVar_hsa_circ_195364,RMVar_hsa_circ_59314,RMVar_hsa_circ_19746,RMVar_hsa_circ_89833,RMVar_hsa_circ_195367,RMVar_hsa_circ_361993,RMVar_hsa_circ_35954 69705 RMVar_ID_69705 Human_SNP_ID_667228726 m1A Human chr19 + 45523693 45523693 45523693 TTGGGGAGAAAACCCCCAAGGATGAATCTGCCAATGTAAGTCAGGGACTCTTCTTGCCCTACATC TTGGGGAGAAAACCCCCAAGGATGAATCTGCCGATGTAAGTCAGGGACTCTTCTTGCCCTACATC A G VASP Ensembl:ENSG00000125753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45522528..45523736 32194978 MeRIP-seq:(Medium) rs761142228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371912,Human_RBP_ID_9346766,Human_RBP_ID_18998154,Human_RBP_ID_19093683,Human_RBP_ID_22665595 Human_Splice_Rec_2019832,Human_Splice_Rec_2019833,Human_Splice_Rec_2019858,Human_Splice_Rec_2019859,Human_Splice_Rec_2019878,Human_Splice_Rec_2019879,Human_Splice_Rec_2019892,Human_Splice_Rec_2019894,Human_Splice_Rec_2019895 RMVar_hsa_circ_37509,RMVar_hsa_circ_110679,RMVar_hsa_circ_195364,RMVar_hsa_circ_59314,RMVar_hsa_circ_19746,RMVar_hsa_circ_89833,RMVar_hsa_circ_195367,RMVar_hsa_circ_361993,RMVar_hsa_circ_35954 69706 RMVar_ID_69706 Human_SNP_ID_667229543 m1A Human chr19 - 45526266 45526266 45526266 GAGTGGGAACGATGCATTCCTGTGTAGTCTTCAGCCAATTCCAAGTCAAGTAGAGGCAGGGAAAG GAGTGGGAACGATGCATTCCTGTGTAGTCTTCCGCCAATTCCAAGTCAAGTAGAGGCAGGGAAAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45526217..45526289 26863196 MeRIP-seq:(Medium) rs767944809 Functional Loss SNV dbSNP153 33..33 33 - - - 69707 RMVar_ID_69707 Human_SNP_ID_667236083 m1A Human chr19 - 45550082 45550082 45550082 GCAATCTCGGCTCACTGCAACTTCTACCTCCCAGGCTCAACCAATGATCCTGCCTCAGCTTCCGA GCAATCTCGGCTCACTGCAACTTCTACCTCCCGGGCTCAACCAATGATCCTGCCTCAGCTTCCGA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1408099284 Functional Loss SNV dbSNP153 33..33 33 - - - 69708 RMVar_ID_69708 Human_SNP_ID_667237040 m1A Human chr19 - 45553644 45553644 45553644 GGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCAGGCGCAGGTGCAGGCGGCGCCGCCACAGGGCG GGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCTGGCGCAGGTGCAGGCGGCGCCGCCACAGGGCG T A OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45553594..45553887 26863196 MeRIP-seq:(Medium) rs372161100 Functional Loss SNV dbSNP153 33..33 33 - - - 69709 RMVar_ID_69709 Human_SNP_ID_667237041 m1A Human chr19 - 45553644 45553644 45553644 GGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCAGGCGCAGGTGCAGGCGGCGCCGCCACAGGGCG GGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCCGGCGCAGGTGCAGGCGGCGCCGCCACAGGGCG T G OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45553594..45553887 26863196 MeRIP-seq:(Medium) rs372161100 Functional Loss SNV dbSNP153 33..33 33 - - - 69710 RMVar_ID_69710 Human_SNP_ID_667238803 m1A Human chr19 - 45560164 45560163 45560164 ACAGATGAAAGGGAGTGAGTCTGGAGGGAGAGAGTTCAGGGAGGAGACGGAAAACGATTCTATGT ACAGATGAAAGGGAGTGAGTCTGGAGGGAGAG_GTTCAGGGAGGAGACGGAAAACGATTCTATGT CT C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45560161..45560249 26863196 MeRIP-seq:(Medium) rs1287023296 Functional Loss DEL dbSNP153 33..33 33 - - - 69711 RMVar_ID_69711 Human_SNP_ID_667245339 m1A Human chr19 - 45582557 45582557 45582557 GCTTCCCCTCACCCATCAAGTTATCCTTAAAAACTCTGCTCCACCGAGATCGCACCACTACACTC GCTTCCCCTCACCCATCAAGTTATCCTTAAAAGCTCTGCTCCACCGAGATCGCACCACTACACTC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45582554..45582664 26863196 MeRIP-seq:(Medium) rs1248216001 Functional Loss SNV dbSNP153 33..33 33 - - - 69712 RMVar_ID_69712 Human_SNP_ID_667245800 m1A Human chr19 - 45584307 45584307 45584307 GAGAGATGGGAGAAATTTGGACGGGGCTTTCCAGGATAGAGGAGCTAGGGGAGGGGCTGAGGAGA GAGAGATGGGAGAAATTTGGACGGGGCTTTCCGGGATAGAGGAGCTAGGGGAGGGGCTGAGGAGA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45584303..45584409 26863196 MeRIP-seq:(Medium) rs1465219401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8490226 69713 RMVar_ID_69713 Human_SNP_ID_667248067 m1A Human chr19 - 45591885 45591885 45591885 CCACAGCCCCCGTGGGCCAGGGGAAGCGCCCCAGAAGCCGAAGTGCCCACCATGGGCAACCACAC CCACAGCCCCCGTGGGCCAGGGGAAGCGCCCCGGAAGCCGAAGTGCCCACCATGGGCAACCACAC T C GPR4,OPA3 Ensembl:ENSG00000177464,Ensembl:ENSG00000125741 Protein coding,Protein coding 5'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45591859..45592010 32194978 MeRIP-seq:(Medium) rs895891805 Functional Loss SNV dbSNP153 33..33 33 - - - 69714 RMVar_ID_69714 Human_SNP_ID_667253045 m1A Human chr19 - 45609648 45609648 45609648 CAGTGGCGGGTGGTCTGATGCGGCCAGGGAAGAGTCAGGTGTCAGGGCAGGAATTCTATTTTCGG CAGTGGCGGGTGGTCTGATGCGGCCAGGGAAGGGTCAGGTGTCAGGGCAGGAATTCTATTTTCGG T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45609487..45609742 26863196 MeRIP-seq:(Medium) rs779017141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523696,Human_RBP_ID_1094978,Human_RBP_ID_5116977,Human_RBP_ID_18166636,Human_RBP_ID_23210982 69715 RMVar_ID_69715 Human_SNP_ID_667254774 m1A Human chr19 + 45615951 45615951 45615951 GCTGCAGAGGGCGGAACCAAGGAGAGGGGGACAGGATTAAATCAGGAAAGTGGAAGTCAAATACA GCTGCAGAGGGCGGAACCAAGGAGAGGGGGACGGGATTAAATCAGGAAAGTGGAAGTCAAATACA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45615905..45616120 26863196 MeRIP-seq:(Medium) rs575624978 Functional Loss SNV dbSNP153 33..33 33 - - - 69716 RMVar_ID_69716 Human_SNP_ID_667254775 m1A Human chr19 + 45615972 45615972 45615972 GAGAGGGGGACAGGATTAAATCAGGAAAGTGGAAGTCAAATACAGAGGTAGGGCGAGAACACAAG GAGAGGGGGACAGGATTAAATCAGGAAAGTGGGAGTCAAATACAGAGGTAGGGCGAGAACACAAG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:45615897..45616002 26863410 MeRIP-seq:(Medium) rs1335619430 Functional Loss SNV dbSNP153 33..33 33 - - - 69717 RMVar_ID_69717 Human_SNP_ID_667256323 m1A Human chr19 + 45621318 45621318 45621318 CCGTGGCCCTCTGCCACGGTGCGCACAGGGCCAAAGTCCTCAGGGACCTGGGTGGACAGATAAGA CCGTGGCCCTCTGCCACGGTGCGCACAGGGCCTAAGTCCTCAGGGACCTGGGTGGACAGATAAGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45621267..45621361 26863196 MeRIP-seq:(Medium) rs1568449133 Functional Loss SNV dbSNP153 33..33 33 - - - 69718 RMVar_ID_69718 Human_SNP_ID_667256325 m1A Human chr19 - 45621322 45621322 45621322 TCCCTCTTATCTGTCCACCCAGGTCCCTGAGGACTTTGGCCCTGTGCGCACCGTGGCAGAGGGCC TCCCTCTTATCTGTCCACCCAGGTCCCTGAGGTCTTTGGCCCTGTGCGCACCGTGGCAGAGGGCC T A EML2 Ensembl:ENSG00000125746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45621068..45621355 26863196 MeRIP-seq:(Medium) rs1255589521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771243,Human_RBP_ID_1295023,Human_RBP_ID_3957139,Human_RBP_ID_5370498,Human_RBP_ID_22446850 Human_Splice_Rec_2019934,Human_Splice_Rec_2019970,Human_Splice_Rec_2019998,Human_Splice_Rec_2020034,Human_Splice_Rec_2020076,Human_Splice_Rec_2020118,Human_Splice_Rec_2020166,Human_Splice_Rec_2020200,Human_Splice_Rec_2020214,Human_Splice_Rec_2020222,Human_Splice_Rec_2020246,Human_Splice_Rec_2020264,Human_Splice_Rec_2020274 RMVar_hsa_circ_372977,RMVar_hsa_circ_34671,RMVar_hsa_circ_195375,RMVar_hsa_circ_125033,RMVar_hsa_circ_195376,RMVar_hsa_circ_195378,RMVar_hsa_circ_108059,RMVar_hsa_circ_109156,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_119263,RMVar_hsa_circ_195377,RMVar_hsa_circ_360373,RMVar_hsa_circ_195380,RMVar_hsa_circ_369417,RMVar_hsa_circ_335056,RMVar_hsa_circ_117472,RMVar_hsa_circ_79035,RMVar_hsa_circ_115644,RMVar_hsa_circ_195382,RMVar_hsa_circ_195383,RMVar_hsa_circ_195384,RMVar_hsa_circ_336759,RMVar_hsa_circ_195386,RMVar_hsa_circ_109902,RMVar_hsa_circ_195385 69719 RMVar_ID_69719 Human_SNP_ID_667256484 m1A Human chr19 - 45621619 45621619 45621619 TGGCCACCCTGCAGGTGGGAACCGTATCACACAGGCGGTGCTGGGCGCCCACGACGGCGGCGTGT TGGCCACCCTGCAGGTGGGAACCGTATCACACCGGCGGTGCTGGGCGCCCACGACGGCGGCGTGT T G EML2 Ensembl:ENSG00000125746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45621476..45621674 26863196 MeRIP-seq:(Medium) rs764086666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955212,Human_RBP_ID_9293805,Human_RBP_ID_22446851 Human_Splice_Rec_2019932,Human_Splice_Rec_2019968,Human_Splice_Rec_2019996,Human_Splice_Rec_2020032,Human_Splice_Rec_2020074,Human_Splice_Rec_2020116,Human_Splice_Rec_2020198,Human_Splice_Rec_2020212,Human_Splice_Rec_2020244,Human_Splice_Rec_2020262,Human_Splice_Rec_2020272,Human_Splice_Rec_2020282 RMVar_hsa_circ_372977,RMVar_hsa_circ_34671,RMVar_hsa_circ_195375,RMVar_hsa_circ_195378,RMVar_hsa_circ_108059,RMVar_hsa_circ_109156,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_119263,RMVar_hsa_circ_195377,RMVar_hsa_circ_360373,RMVar_hsa_circ_195380,RMVar_hsa_circ_369417,RMVar_hsa_circ_335056,RMVar_hsa_circ_117472,RMVar_hsa_circ_79035,RMVar_hsa_circ_115644,RMVar_hsa_circ_195382,RMVar_hsa_circ_195383,RMVar_hsa_circ_195384,RMVar_hsa_circ_336759,RMVar_hsa_circ_80918,RMVar_hsa_circ_195386,RMVar_hsa_circ_195387 69720 RMVar_ID_69720 Human_SNP_ID_667257230 m1A Human chr19 - 45624739 45624739 45624739 TGGCGACGTGGTCACGGGGGACTCTGGGGGGAACCTCTATGTTTGGGGCAAAGGTCAGTGTCACC TGGCGACGTGGTCACGGGGGACTCTGGGGGGATCCTCTATGTTTGGGGCAAAGGTCAGTGTCACC T A EML2 Ensembl:ENSG00000125746 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45621149..45624763 32194978 MeRIP-seq:(Medium) rs1490305609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913473,Human_RBP_ID_3955213,Human_RBP_ID_8840130,Human_RBP_ID_18995136,Human_RBP_ID_22446852 Human_Splice_Rec_2019930,Human_Splice_Rec_2019931,Human_Splice_Rec_2019966,Human_Splice_Rec_2019967,Human_Splice_Rec_2019994,Human_Splice_Rec_2019995,Human_Splice_Rec_2020030,Human_Splice_Rec_2020031,Human_Splice_Rec_2020072,Human_Splice_Rec_2020073,Human_Splice_Rec_2020114,Human_Splice_Rec_2020115,Human_Splice_Rec_2020164,Human_Splice_Rec_2020165,Human_Splice_Rec_2020196,Human_Splice_Rec_2020197,Human_Splice_Rec_2020211,Human_Splice_Rec_2020242,Human_Splice_Rec_2020243,Human_Splice_Rec_2020270,Human_Splice_Rec_2020271,Human_Splice_Rec_2020280,Human_Splice_Rec_2020281,Human_Splice_Rec_2020288,Human_Splice_Rec_2020289,Human_Splice_Rec_2020298 RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_195378,RMVar_hsa_circ_108059,RMVar_hsa_circ_109156,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_119263,RMVar_hsa_circ_195377,RMVar_hsa_circ_360373,RMVar_hsa_circ_195380,RMVar_hsa_circ_369417,RMVar_hsa_circ_335056,RMVar_hsa_circ_117472,RMVar_hsa_circ_79035,RMVar_hsa_circ_115644,RMVar_hsa_circ_195382,RMVar_hsa_circ_195383,RMVar_hsa_circ_195384,RMVar_hsa_circ_336759,RMVar_hsa_circ_80918,RMVar_hsa_circ_195386,RMVar_hsa_circ_17504,RMVar_hsa_circ_195387,RMVar_hsa_circ_370552,RMVar_hsa_circ_195388 69721 RMVar_ID_69721 Human_SNP_ID_667259639 m1A Human chr19 + 45633131 45633131 45633131 GTCCCGTGGCGATGGTGACCATATCTGGGTGGATGGCCAAGCTGCGGAAAGAAGGGACAGAGAGA GTCCCGTGGCGATGGTGACCATATCTGGGTGGGTGGCCAAGCTGCGGAAAGAAGGGACAGAGAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45633081..45634463 32194978 MeRIP-seq:(Medium) rs781551226 Functional Loss SNV dbSNP153 33..33 33 - - - 69722 RMVar_ID_69722 Human_SNP_ID_667261550 m1A Human chr19 - 45639301 45639301 45639301 CCCCATCTCCTCTCCGCGCTCCCGGGGCTTAGATCTCAGGTTTCACCCAACCCCTGGGACCCAGA CCCCATCTCCTCTCCGCGCTCCCGGGGCTTAGGTCTCAGGTTTCACCCAACCCCTGGGACCCAGA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45639298..45639400 26863196 MeRIP-seq:(Medium) rs1049734495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2020315,Human_Splice_Rec_2020349 RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_112744,RMVar_hsa_circ_104362,RMVar_hsa_circ_111786,RMVar_hsa_circ_127436,RMVar_hsa_circ_109853,RMVar_hsa_circ_92289,RMVar_hsa_circ_195391,RMVar_hsa_circ_195393,RMVar_hsa_circ_195394,RMVar_hsa_circ_195392,RMVar_hsa_circ_195390,RMVar_hsa_circ_195400,RMVar_hsa_circ_96749,RMVar_hsa_circ_195401 69723 RMVar_ID_69723 Human_SNP_ID_667262365 m1A Human chr19 - 45642025 45642025 45642025 AACCCCATCCCTCCAGTGTGTCAGCTCTTGAAAGGCCTTCCCACCAGGACGCCCCTTAATGGCTC AACCCCATCCCTCCAGTGTGTCAGCTCTTGAAGGGCCTTCCCACCAGGACGCCCCTTAATGGCTC T C EML2 Ensembl:ENSG00000125746 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45641852..45642050 26863196 MeRIP-seq:(Medium) rs1568497271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2020054,Human_Splice_Rec_2020096,Human_Splice_Rec_2020178,Human_Splice_Rec_2020326,Human_Splice_Rec_2020366 RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_112744,RMVar_hsa_circ_104362,RMVar_hsa_circ_111786,RMVar_hsa_circ_127436,RMVar_hsa_circ_109853,RMVar_hsa_circ_92289,RMVar_hsa_circ_195391,RMVar_hsa_circ_195393,RMVar_hsa_circ_195394,RMVar_hsa_circ_195392,RMVar_hsa_circ_195390,RMVar_hsa_circ_195401,RMVar_hsa_circ_19763 69724 RMVar_ID_69724 Human_SNP_ID_667262370 m1A Human chr19 - 45642035 45642035 45642035 TCTGTCCCCTAACCCCATCCCTCCAGTGTGTCAGCTCTTGAAAGGCCTTCCCACCAGGACGCCCC TCTGTCCCCTAACCCCATCCCTCCAGTGTGTCGGCTCTTGAAAGGCCTTCCCACCAGGACGCCCC T C EML2 Ensembl:ENSG00000125746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr19:45641874..45642047;chr19:45641911..45642038 26863196 MeRIP-seq:(Medium) rs1422518007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2020054,Human_Splice_Rec_2020096,Human_Splice_Rec_2020178,Human_Splice_Rec_2020326,Human_Splice_Rec_2020366 RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_112744,RMVar_hsa_circ_104362,RMVar_hsa_circ_111786,RMVar_hsa_circ_127436,RMVar_hsa_circ_109853,RMVar_hsa_circ_92289,RMVar_hsa_circ_195391,RMVar_hsa_circ_195393,RMVar_hsa_circ_195394,RMVar_hsa_circ_195392,RMVar_hsa_circ_195390,RMVar_hsa_circ_195401,RMVar_hsa_circ_19763 69725 RMVar_ID_69725 Human_SNP_ID_667270918 m1A Human chr19 + 45671073 45671073 45671073 GTTTGGTGGGAGGAGCCCAGAGTGGGGCCGGGAGGAGGGGCGGAGCTTTGAGGCTGGTGGGAGGA GTTTGGTGGGAGGAGCCCAGAGTGGGGCCGGGTGGAGGGGCGGAGCTTTGAGGCTGGTGGGAGGA A T GIPR Ensembl:ENSG00000010310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45671069..45671163 26863196 MeRIP-seq:(Medium) rs1443758798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203598,Human_RBP_ID_263294,Human_RBP_ID_824437,Human_RBP_ID_907872,Human_RBP_ID_3581388,Human_RBP_ID_3955224,Human_RBP_ID_5145801,Human_RBP_ID_5192313,Human_RBP_ID_5320457,Human_RBP_ID_8100742,Human_RBP_ID_8197836,Human_RBP_ID_8233489,Human_RBP_ID_8942224,Human_RBP_ID_9294460,Human_RBP_ID_9426255,Human_RBP_ID_17131950,Human_RBP_ID_18421584,Human_RBP_ID_18490819,Human_RBP_ID_19095174,Human_RBP_ID_21978053,Human_RBP_ID_22476930,Human_RBP_ID_22662853,Human_RBP_ID_22718379,Human_RBP_ID_24545676,Human_RBP_ID_24552945,Human_RBP_ID_26336423,Human_RBP_ID_26783793,Human_RBP_ID_27815507,Human_RBP_ID_27839578 69726 RMVar_ID_69726 Human_SNP_ID_667272863 m1A Human chr19 + 45677073 45677073 45677073 CAGTCTCCTGGTGCTCGTGGGAGGCTCCGAGGAGGGCCACTTCCGCTACTACCTGCTCCTCGGCT CAGTCTCCTGGTGCTCGTGGGAGGCTCCGAGGTGGGCCACTTCCGCTACTACCTGCTCCTCGGCT A T GIPR Ensembl:ENSG00000010310 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45677069..45677134 26863196 MeRIP-seq:(Medium) rs192821802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22476665 Human_Splice_Rec_2020395,Human_Splice_Rec_2020421,Human_Splice_Rec_2020447,Human_Splice_Rec_2020469,Human_Splice_Rec_2020495 RMVar_hsa_circ_1658,RMVar_hsa_circ_363500,RMVar_hsa_circ_195404,RMVar_hsa_circ_327432 69727 RMVar_ID_69727 Human_SNP_ID_667275878 m1A Human chr19 - 45687595 45687595 45687595 TACATCTCCAAGATGTTCCTGCGCGGGGACTCAGTCATCGTGGTCCTGCGGAACCCGCTCATCGC TACATCTCCAAGATGTTCCTGCGCGGGGACTCGGTCATCGTGGTCCTGCGGAACCCGCTCATCGC T C SNRPD2 Ensembl:ENSG00000125743 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45687545..45687650 26863196 MeRIP-seq:(Medium) rs772089761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240015,Human_RBP_ID_523715,Human_RBP_ID_771234,Human_RBP_ID_1568331,Human_RBP_ID_1890097,Human_RBP_ID_4537047,Human_RBP_ID_5116316,Human_RBP_ID_8490246,Human_RBP_ID_9088809,Human_RBP_ID_9329035,Human_RBP_ID_17655369,Human_RBP_ID_18192320,Human_RBP_ID_18735840,Human_RBP_ID_22447880,Human_RBP_ID_23801330,Human_RBP_ID_26816016,Human_RBP_ID_26991752,Human_RBP_ID_27275733 Human_miRNA_ID_1998958 RMVar_hsa_circ_195407,RMVar_hsa_circ_105248,RMVar_hsa_circ_121142,RMVar_hsa_circ_123868,RMVar_hsa_circ_113835,RMVar_hsa_circ_195409,RMVar_hsa_circ_195410,RMVar_hsa_circ_195408 69728 RMVar_ID_69728 Human_SNP_ID_667276155 m1A Human chr19 - 45688555 45688555 45688555 GTTCCATGTTTGTCCATGCAGGAGCCTCCTCAACAAGCCCAAGAGTGAGATGACCCCAGAGGAGC GTTCCATGTTTGTCCATGCAGGAGCCTCCTCAGCAAGCCCAAGAGTGAGATGACCCCAGAGGAGC T C SNRPD2 Ensembl:ENSG00000125743 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:45688501..45688600 26863410 MeRIP-seq:(Medium) rs972073403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523731,Human_RBP_ID_771237,Human_RBP_ID_1568343,Human_RBP_ID_5116318,Human_RBP_ID_5376977,Human_RBP_ID_9381146,Human_RBP_ID_17656255,Human_RBP_ID_18420953,Human_RBP_ID_22449528,Human_RBP_ID_26334935,Human_RBP_ID_26816029 Human_Splice_Rec_2020514,Human_Splice_Rec_2020524,Human_Splice_Rec_2020528,Human_Splice_Rec_2020534,Human_Splice_Rec_2020540,Human_Splice_Rec_2020544 RMVar_hsa_circ_121142,RMVar_hsa_circ_123868,RMVar_hsa_circ_113835,RMVar_hsa_circ_195409,RMVar_hsa_circ_195410,RMVar_hsa_circ_195408,RMVar_hsa_circ_195411,RMVar_hsa_circ_310432 69729 RMVar_ID_69729 Human_SNP_ID_667277145 m1A Human chr19 + 45691828 45691828 45691828 CCCCCCGCTCTGCTCAACCCTTCCCACACTCAATCGGTCAAATATCCACCCTCAACCTCATTCCC CCCCCCGCTCTGCTCAACCCTTCCCACACTCAGTCGGTCAAATATCCACCCTCAACCTCATTCCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45691817..45691950 26863410 MeRIP-seq:(Medium) rs986801377 Functional Loss SNV dbSNP153 33..33 33 - - - 69730 RMVar_ID_69730 Human_SNP_ID_667277481 m1A Human chr19 - 45692735 45692735 45692735 GTGGCTCCATGAGGCCACGTTCCCCCAGCCGCAGGCGGGGTCGCCCGCGGCCCCCGGAACGCATG GTGGCTCCATGAGGCCACGTTCCCCCAGCCGCGGGCGGGGTCGCCCGCGGCCCCCGGAACGCATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45692686..45692801 26863196 MeRIP-seq:(Medium) rs1359588733 Functional Loss SNV dbSNP153 33..33 33 - - - 69731 RMVar_ID_69731 Human_SNP_ID_667277492 m1A Human chr19 + 45692748 45692748 45692748 GGCCGCGGGCGACCCCGCCTGCGGCTGGGGGAACGTGGCCTCATGGAGCCACTCTTGCCGCCGAA GGCCGCGGGCGACCCCGCCTGCGGCTGGGGGAGCGTGGCCTCATGGAGCCACTCTTGCCGCCGAA A G QPCTL Ensembl:ENSG00000011478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45692701..45692843 26863196 MeRIP-seq:(Medium) rs932148233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557594,Human_RBP_ID_22447882 69732 RMVar_ID_69732 Human_SNP_ID_667277496 m1A Human chr19 - 45692756 45692756 45692756 GGCGGCGCTTCGGCGGCAAGAGTGGCTCCATGAGGCCACGTTCCCCCAGCCGCAGGCGGGGTCGC GGCGGCGCTTCGGCGGCAAGAGTGGCTCCATGGGGCCACGTTCCCCCAGCCGCAGGCGGGGTCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45692707..45692860 26863196 MeRIP-seq:(Medium) rs1254686337 Functional Loss SNV dbSNP153 33..33 33 - - - 69733 RMVar_ID_69733 Human_SNP_ID_667277759 m1A Human chr19 + 45693530 45693530 45693530 TGCGCCCCCTGCTGGTTGTGCGAACCCCGGGCAGCCCGGGAAATCTCCAAGTCAGAAAGGTAAAG TGCGCCCCCTGCTGGTTGTGCGAACCCCGGGCTGCCCGGGAAATCTCCAAGTCAGAAAGGTAAAG A T QPCTL Ensembl:ENSG00000011478 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45693483..45695514 32194978 MeRIP-seq:(Medium) rs776405328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5376979,Human_RBP_ID_18998172,Human_RBP_ID_22447886 Human_Splice_Rec_2020551,Human_Splice_Rec_2020563,Human_Splice_Rec_2020573 69734 RMVar_ID_69734 Human_SNP_ID_667279189 m1A Human chr19 + 45698670 45698670 45698670 ACCTGGCCCAGCTCATGGAGTCTATACCTCACAGCCCCGGCCCCACCAGGATCCAGGCTATTGTA ACCTGGCCCAGCTCATGGAGTCTATACCTCACGGCCCCGGCCCCACCAGGATCCAGGCTATTGTA A G QPCTL Ensembl:ENSG00000011478 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45698623..45698806 32194978 MeRIP-seq:(Medium) rs1292853538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22594159 Human_Splice_Rec_2020555,Human_Splice_Rec_2020565,Human_Splice_Rec_2020577,Human_Splice_Rec_2020579 Human_miRNA_ID_2007829,Human_miRNA_ID_2673466 RMVar_hsa_circ_116521,RMVar_hsa_circ_280704,RMVar_hsa_circ_195412,RMVar_hsa_circ_195413 69735 RMVar_ID_69735 Human_SNP_ID_667280790 m1A Human chr19 + 45703902 45703902 45703902 TTGTACGCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAAC TTGTACGCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCAAC A G QPCTL Ensembl:ENSG00000011478 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1446492382 Functional Loss SNV dbSNP153 33..33 33 - - - 69736 RMVar_ID_69736 Human_SNP_ID_667283504 m1A Human chr19 + 45712818 45712818 45712818 TGCGCTTCAAAGTGGGCCACGGCCTCGGCTACACGGCTGCAGTCCCCACCACCGGACCGCCGTTC TGCGCTTCAAAGTGGGCCACGGCCTCGGCTACCCGGCTGCAGTCCCCACCACCGGACCGCCGTTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45712769..45712853 26863196 MeRIP-seq:(Medium) rs1436035649 Functional Loss SNV dbSNP153 33..33 33 - - - 69737 RMVar_ID_69737 Human_SNP_ID_667284658 m1A Human chr19 - 45716510 45716510 45716510 TATGACATAGTTTGGGGAATTGCTGTGTTGGGATCTGTGAGAGATTGACTGAGATTCGGCCCTTC TATGACATAGTTTGGGGAATTGCTGTGTTGGGGTCTGTGAGAGATTGACTGAGATTCGGCCCTTC T C AC007191.1,FBXO46 Ensembl:ENSG00000279407,Ensembl:ENSG00000177051 Other,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45716505..45716590 26863196 MeRIP-seq:(Medium) rs1308189716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523768,Human_RBP_ID_3589147,Human_RBP_ID_5587415,Human_RBP_ID_6773837,Human_RBP_ID_8835497,Human_RBP_ID_13475947,Human_RBP_ID_17134152,Human_RBP_ID_18735867,Human_RBP_ID_23801360,Human_RBP_ID_27681757 Human_miRNA_ID_3163464 69738 RMVar_ID_69738 Human_SNP_ID_667284820 m1A Human chr19 - 45717155 45717155 45717155 ACAAGATTTGGGGGTTCCTTTTCCATTTGCAAAATGTTCTGGGGCTTGGGGAAGTTTTAACGTGG ACAAGATTTGGGGGTTCCTTTTCCATTTGCAAGATGTTCTGGGGCTTGGGGAAGTTTTAACGTGG T C AC007191.1,FBXO46 Ensembl:ENSG00000279407,Ensembl:ENSG00000177051 Other,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45717152..45717309 26863196 MeRIP-seq:(Medium) rs1031527937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5088829,Human_RBP_ID_6773846,Human_RBP_ID_9426259 69739 RMVar_ID_69739 Human_SNP_ID_667286085 m1A Human chr19 - 45722116 45722115 45722116 GAGCAGCAGGGTAGGGCATAGAAGGAACAGGGACCGGGCGCGGTGCATCATGCCTGTAATCCCAG GAGCAGCAGGGTAGGGCATAGAAGGAACAGGG_CCGGGCGCGGTGCATCATGCCTGTAATCCCAG GT G FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45722110..45722277 26863196 MeRIP-seq:(Medium) rs1473005037 Functional Loss DEL dbSNP153 33..33 33 - - - 69740 RMVar_ID_69740 Human_SNP_ID_667297378 m1A Human chr19 - 45765827 45765827 45765827 AGCCACCCCCCGCCGCTGCCACCACCTCCAGCACCAGCCTGCCCTTCTCCCCTGACTCCCCTGGC AGCCACCCCCCGCCGCTGCCACCACCTCCAGCCCCAGCCTGCCCTTCTCCCCTGACTCCCCTGGC T G SIX5 Ensembl:ENSG00000177045 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45765776..45766050 26863196 MeRIP-seq:(Medium) rs182338540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27469220 Human_miRNA_ID_272468,Human_miRNA_ID_2052801 RMVar_hsa_circ_124896,RMVar_hsa_circ_195415 69741 RMVar_ID_69741 Human_SNP_ID_667298942 m1A Human chr19 - 45768772 45768772 45768772 CTGGGGGGGAGGCGGTGGCGGCGGCGGCGGCGACCGAAGAGGAGGAGGAGGAAGCGCGCCAGCTC CTGGGGGGGAGGCGGTGGCGGCGGCGGCGGCGGCCGAAGAGGAGGAGGAGGAAGCGCGCCAGCTC T C SIX5 Ensembl:ENSG00000177045 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:45768680..45768851 26863196 MeRIP-seq:(Medium) rs1568566351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330139,Human_RBP_ID_21978054,Human_RBP_ID_22072010,Human_RBP_ID_22720150 Human_Splice_Rec_2020621 69742 RMVar_ID_69742 Human_SNP_ID_667299001 m1A Human chr19 + 45768862 45768862 45768862 AGGCAAGGTAGCCATGTTTTGCAACTTTGGGAAGTTCCTCCCTCCCTCTCTTCCTCCCTCGGGCT AGGCAAGGTAGCCATGTTTTGCAACTTTGGGAGGTTCCTCCCTCCCTCTCTTCCTCCCTCGGGCT A G DM1-AS,AC074212.1 Ensembl:ENSG00000267395,Ensembl:ENSG00000259605 lincRNA,lincRNA intron,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45768662..45769005 26863410 MeRIP-seq:(Medium) rs1220464659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912169,Human_RBP_ID_18947091 69743 RMVar_ID_69743 Human_SNP_ID_667299025 m1A Human chr19 + 45768901 45768901 45768901 CCCTCCCTCTCTTCCTCCCTCGGGCTTTCCCCAGCCTCCTCCCCCACCTGTCCCCCCTTTTCGCC CCCTCCCTCTCTTCCTCCCTCGGGCTTTCCCCCGCCTCCTCCCCCACCTGTCCCCCCTTTTCGCC A C DM1-AS,AC074212.1 Ensembl:ENSG00000267395,Ensembl:ENSG00000259605 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45768672..45769125 26863196 MeRIP-seq:(Medium) rs1478044380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824608,Human_RBP_ID_8199755,Human_RBP_ID_18947091 69744 RMVar_ID_69744 Human_SNP_ID_667299052 m1A Human chr19 + 45768937 45768937 45768937 TCCTCCCCCACCTGTCCCCCCTTTTCGCCCCCACTCCCCGCTCTTCTCGATCTTCTTTCTGGCCG TCCTCCCCCACCTGTCCCCCCTTTTCGCCCCCCCTCCCCGCTCTTCTCGATCTTCTTTCTGGCCG A C DM1-AS,AC074212.1 Ensembl:ENSG00000267395,Ensembl:ENSG00000259605 lincRNA,lincRNA intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:45768676..45769061 26863196 MeRIP-seq:(Medium) rs1285785204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18947092 69745 RMVar_ID_69745 Human_SNP_ID_667299114 m1A Human chr19 - 45769070 45769069 45769071 AGAAAGCGCGGCCAGAGGCGGAGGGAAAACAAAGGGAGAATCACAGACAGACGGGAGGGGGACGG AGAAAGCGCGGCCAGAGGCGGAGGGAAAACA__GGGAGAATCACAGACAGACGGGAGGGGGACGG CTT C SIX5 Ensembl:ENSG00000177045 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45765466..45769275 26863196 MeRIP-seq:(Medium) rs1225314610 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9428283 69746 RMVar_ID_69746 Human_SNP_ID_667299400 m1A Human chr19 - 45769593 45769592 45769593 TGGGAGGAGCTAGCGGGATGCGAAGCGGCCGAATCAGGGTTGGGGGAGGAAAAGCCACGGGGCGG TGGGAGGAGCTAGCGGGATGCGAAGCGGCCGA_TCAGGGTTGGGGGAGGAAAAGCCACGGGGCGG AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45769545..45769628 26863196 MeRIP-seq:(Medium) rs932343534 Functional Loss DEL dbSNP153 33..33 33 - - - 69747 RMVar_ID_69747 Human_SNP_ID_667299509 m1A Human chr19 + 45769796 45769796 45769796 TCCTAGGTGGGGACAGACAATAAATACCGAGGAATGTCGGGGTCTCAGTGCATCCAAAACGTGGA TCCTAGGTGGGGACAGACAATAAATACCGAGGGATGTCGGGGTCTCAGTGCATCCAAAACGTGGA A G DM1-AS,AC074212.1 Ensembl:ENSG00000267395,Ensembl:ENSG00000259605 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45769751..45769970 26863196 MeRIP-seq:(Medium) rs1164528842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2567444 69748 RMVar_ID_69748 Human_SNP_ID_667299542 m1A Human chr19 + 45769875 45769875 45769875 GGTCCTGTAGCCTGTCAGCGAGTCGGAGGACGAGGTCAATAAATATCCAAACCGCCGAAGCGGGC GGTCCTGTAGCCTGTCAGCGAGTCGGAGGACGGGGTCAATAAATATCCAAACCGCCGAAGCGGGC A G DM1-AS Ensembl:ENSG00000267395 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr19:45769776..45770000;chr19:45769826..45770000;chr19:45769773..45769933 26863196,26863410 MeRIP-seq:(Medium) rs573665770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587038 69749 RMVar_ID_69749 Human_SNP_ID_667300281 m1A Human chr19 - 45771029 45771029 45771029 GCTAGATGGCCCCCCGGCCGTGGCTGTGGGCCAGTGCCCGCTGGTGGGGCCAGGCCCCATGCACC GCTAGATGGCCCCCCGGCCGTGGCTGTGGGCCCGTGCCCGCTGGTGGGGCCAGGCCCCATGCACC T G DMPK Ensembl:ENSG00000104936 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45770978..45771080 26863196 MeRIP-seq:(Medium) rs569811181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911599,Human_RBP_ID_3955230,Human_RBP_ID_5117759 Human_Splice_Rec_2020662,Human_Splice_Rec_2020663,Human_Splice_Rec_2020690,Human_Splice_Rec_2020691,Human_Splice_Rec_2020720,Human_Splice_Rec_2020721,Human_Splice_Rec_2020744,Human_Splice_Rec_2020745,Human_Splice_Rec_2020770,Human_Splice_Rec_2020771,Human_Splice_Rec_2020796,Human_Splice_Rec_2020797,Human_Splice_Rec_2020824,Human_Splice_Rec_2020825,Human_Splice_Rec_2020852,Human_Splice_Rec_2020853,Human_Splice_Rec_2020880,Human_Splice_Rec_2020881 69750 RMVar_ID_69750 Human_SNP_ID_667300479 m1A Human chr19 + 45771355 45771355 45771355 GAGGCAGGGGAAAGAGAGGGGTCTTACATGGGAAGGTGGATCCGTGGCCCGGGGACTGGGGACCC GAGGCAGGGGAAAGAGAGGGGTCTTACATGGGCAGGTGGATCCGTGGCCCGGGGACTGGGGACCC A C DM1-AS Ensembl:ENSG00000267395 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45770987..45771496 32194978 MeRIP-seq:(Medium) rs1444054450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581392,Human_RBP_ID_5587045 69751 RMVar_ID_69751 Human_SNP_ID_667300492 m1A Human chr19 - 45771391 45771382 45771391 CCCTATGCCTCTTTCTTCTCCTTCCAGCTGTCACGGGGGTCCCCAGTCCCCGGGCCACGGATCCA CCCTATGCCTCTTTCTTCTCCTTCCAGCTGTC_________CCCAGTCCCCGGGCCACGGATCCA GGACCCCCGT G DMPK Ensembl:ENSG00000104936 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45771280..45771463 26863196 MeRIP-seq:(Medium) rs1327287684 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_3955231,Human_RBP_ID_18995142,Human_RBP_ID_25425405 Human_Splice_Rec_2020660,Human_Splice_Rec_2020661,Human_Splice_Rec_2020688,Human_Splice_Rec_2020689,Human_Splice_Rec_2020718,Human_Splice_Rec_2020719,Human_Splice_Rec_2020742,Human_Splice_Rec_2020743,Human_Splice_Rec_2020768,Human_Splice_Rec_2020769,Human_Splice_Rec_2020794,Human_Splice_Rec_2020795,Human_Splice_Rec_2020822,Human_Splice_Rec_2020823,Human_Splice_Rec_2020850,Human_Splice_Rec_2020851,Human_Splice_Rec_2020878,Human_Splice_Rec_2020879,Human_Splice_Rec_2020920 69752 RMVar_ID_69752 Human_SNP_ID_667300661 m1A Human chr19 - 45771677 45771677 45771677 TCTCGTCCGGCCCGGACGGACTCACCGTCCTTACCTCCCCACAGTCAACTACGCGAGGCAGAGGC TCTCGTCCGGCCCGGACGGACTCACCGTCCTTGCCTCCCCACAGTCAACTACGCGAGGCAGAGGC T C DMPK Ensembl:ENSG00000104936 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45771675..45771785 26863196 MeRIP-seq:(Medium) rs1337903623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50544 69753 RMVar_ID_69753 Human_SNP_ID_667300942 m1A Human chr19 - 45772366 45772366 45772366 AGGAGAAACAAGCCATGGAAGGAAAGGTGCCAAGTGGTCAGGCGAGAGCCTCCAGGGCAAAGGCC AGGAGAAACAAGCCATGGAAGGAAAGGTGCCAGGTGGTCAGGCGAGAGCCTCCAGGGCAAAGGCC T C DMPK Ensembl:ENSG00000104936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45772364..45772539 26863196 MeRIP-seq:(Medium) rs753086131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50544 69754 RMVar_ID_69754 Human_SNP_ID_667300943 m1A Human chr19 - 45772366 45772366 45772366 AGGAGAAACAAGCCATGGAAGGAAAGGTGCCAAGTGGTCAGGCGAGAGCCTCCAGGGCAAAGGCC AGGAGAAACAAGCCATGGAAGGAAAGGTGCCACGTGGTCAGGCGAGAGCCTCCAGGGCAAAGGCC T G DMPK Ensembl:ENSG00000104936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45772364..45772539 26863196 MeRIP-seq:(Medium) rs753086131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50544 69755 RMVar_ID_69755 Human_SNP_ID_667302660 m1A Human chr19 + 45777758 45777758 45777758 GCCCATAGAACATTTCATAGGCGAATACACCCAGCGCCCACCAGTCACACTCGGGCCCGTAGCTG GCCCATAGAACATTTCATAGGCGAATACACCCCGCGCCCACCAGTCACACTCGGGCCCGTAGCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45777710..45777823 26863196 MeRIP-seq:(Medium) rs751334898 Functional Loss SNV dbSNP153 33..33 33 - - - 69756 RMVar_ID_69756 Human_SNP_ID_667303341 m1A Human chr19 - 45779447 45779446 45779447 TGAAGATCATGAACAAGTGGGACATGCTGAAGAGGGGCGAGGTGAGGGGCTGGGCGGACGTGGGG TGAAGATCATGAACAAGTGGGACATGCTGAAG_GGGGCGAGGTGAGGGGCTGGGCGGACGTGGGG CT C DMPK,AC011530.1 Ensembl:ENSG00000104936,Ensembl:ENSG00000268434 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45779144..45779539 26863196 MeRIP-seq:(Medium) rs1323220103 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5585799 Human_Splice_Rec_2020640,Human_Splice_Rec_2020641,Human_Splice_Rec_2020668,Human_Splice_Rec_2020669,Human_Splice_Rec_2020698,Human_Splice_Rec_2020699,Human_Splice_Rec_2020723,Human_Splice_Rec_2020748,Human_Splice_Rec_2020749,Human_Splice_Rec_2020774,Human_Splice_Rec_2020775,Human_Splice_Rec_2020802,Human_Splice_Rec_2020803,Human_Splice_Rec_2020830,Human_Splice_Rec_2020831,Human_Splice_Rec_2020858,Human_Splice_Rec_2020859,Human_Splice_Rec_2020886,Human_Splice_Rec_2020887,Human_Splice_Rec_2020942,Human_Splice_Rec_2020943,Human_Splice_Rec_2020948,Human_Splice_Rec_2020949,Human_Splice_Rec_2020953,Human_Splice_Rec_2020958,Human_Splice_Rec_2020966,Human_Splice_Rec_2020972,Human_Splice_Rec_2020978 RMVar_hsa_circ_50544,RMVar_hsa_circ_65614,RMVar_hsa_circ_377524 69757 RMVar_ID_69757 Human_SNP_ID_667303511 m1A Human chr19 - 45779768 45779768 45779768 TCGGACGCGGGGCGTTCAGCGAGGTAAGCCGAACCGGGCGGGAGCCTGACTTGACTCGTGGTGGG TCGGACGCGGGGCGTTCAGCGAGGTAAGCCGAGCCGGGCGGGAGCCTGACTTGACTCGTGGTGGG T C DMPK,AC011530.1 Ensembl:ENSG00000104936,Ensembl:ENSG00000268434 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45779764..45779909 26863196 MeRIP-seq:(Medium) rs761250462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50544,RMVar_hsa_circ_65614 69758 RMVar_ID_69758 Human_SNP_ID_667304282 m1A Human chr19 - 45781975 45781975 45781975 TCTGGAGGGGCAGAGTAAGGTCAGCAGAGGCTAGGGTGGCTGTGACTCAGAGCCATGGCTTAGGA TCTGGAGGGGCAGAGTAAGGTCAGCAGAGGCTGGGGTGGCTGTGACTCAGAGCCATGGCTTAGGA T C DMPK,AC011530.1 Ensembl:ENSG00000104936,Ensembl:ENSG00000268434 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45781970..45782083 26863196 MeRIP-seq:(Medium) rs1389133811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241263,Human_RBP_ID_1190674,Human_RBP_ID_19090446 69759 RMVar_ID_69759 Human_SNP_ID_667305121 m1A Human chr19 - 45784164 45784164 45784164 GCCATAACCCTCCCTGCTGACCTCACAGATCAACGTATTAACAAGACTAACCATGATGGATGGAC GCCATAACCCTCCCTGCTGACCTCACAGATCAGCGTATTAACAAGACTAACCATGATGGATGGAC T C DMWD,AC011530.1 Ensembl:ENSG00000185800,Ensembl:ENSG00000268434 Protein coding,Protein coding 3'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45784087..45784188 26863410 MeRIP-seq:(Medium) rs768191989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1890146,Human_RBP_ID_13476383,Human_RBP_ID_21930263,Human_RBP_ID_26991875 69760 RMVar_ID_69760 Human_SNP_ID_667305122 m1A Human chr19 - 45784164 45784164 45784164 GCCATAACCCTCCCTGCTGACCTCACAGATCAACGTATTAACAAGACTAACCATGATGGATGGAC GCCATAACCCTCCCTGCTGACCTCACAGATCACCGTATTAACAAGACTAACCATGATGGATGGAC T G DMWD,AC011530.1 Ensembl:ENSG00000185800,Ensembl:ENSG00000268434 Protein coding,Protein coding 3'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45784087..45784188 26863410 MeRIP-seq:(Medium) rs768191989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1890146,Human_RBP_ID_13476383,Human_RBP_ID_21930263,Human_RBP_ID_26991875 69761 RMVar_ID_69761 Human_SNP_ID_667305859 m1A Human chr19 - 45786101 45786092 45786101 CCCCTGGCCCGCACCCGCACCCTCCCTGGCACACCTGGCACCACGCCACCGGCCGCCAGCAGCTC CCCCTGGCCCGCACCCGCACCCTCCCTGGCAC_________CACGCCACCGGCCGCCAGCAGCTC GGTGCCAGGT G DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45785868..45786117 26863410 MeRIP-seq:(Medium) rs1164041852 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_18193106 69762 RMVar_ID_69762 Human_SNP_ID_667305866 m1A Human chr19 - 45786103 45786103 45786103 CCCCCCTGGCCCGCACCCGCACCCTCCCTGGCACACCTGGCACCACGCCACCGGCCGCCAGCAGC CCCCCCTGGCCCGCACCCGCACCCTCCCTGGCGCACCTGGCACCACGCCACCGGCCGCCAGCAGC T C DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45786055..45786133 26863196 MeRIP-seq:(Medium) rs1325677803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18193106 69763 RMVar_ID_69763 Human_SNP_ID_667305885 m1A Human chr19 - 45786121 45786121 45786121 ACGTGCTCTACCCGCACCCCCCCCTGGCCCGCACCCGCACCCTCCCTGGCACACCTGGCACCACG ACGTGCTCTACCCGCACCCCCCCCTGGCCCGCCCCCGCACCCTCCCTGGCACACCTGGCACCACG T G DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45786077..45786256 26863196 MeRIP-seq:(Medium) rs1273820821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5376989,Human_RBP_ID_18193106,Human_RBP_ID_22072015 69764 RMVar_ID_69764 Human_SNP_ID_667306038 m1A Human chr19 - 45786347 45786347 45786347 GCTGTGGCCTTTGACCCCTACACCACAAGGGCAGAGGAGGCGGCGACAGCAGCCGGTGCTGATGG GCTGTGGCCTTTGACCCCTACACCACAAGGGCGGAGGAGGCGGCGACAGCAGCCGGTGCTGATGG T C DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45786297..45786399 26863196 MeRIP-seq:(Medium) rs1445393073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527052,Human_RBP_ID_17928011 69765 RMVar_ID_69765 Human_SNP_ID_667307828 m1A Human chr19 - 45792425 45792425 45792425 CCTCGGGGAGCCGGACAGCGCCGGGGCCGGGGAGCCGCCCGCCACGCCCGCGGGGCTGGGCTCGG CCTCGGGGAGCCGGACAGCGCCGGGGCCGGGGTGCCGCCCGCCACGCCCGCGGGGCTGGGCTCGG T A DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45792376..45792788 26863196 MeRIP-seq:(Medium) rs1362802690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241948,Human_RBP_ID_4557600,Human_RBP_ID_9329043,Human_RBP_ID_22533176 69766 RMVar_ID_69766 Human_SNP_ID_667307861 m1A Human chr19 - 45792499 45792499 45792499 CCCGCGTCGTCCCCGCCGCCCGCAGGCCCCGGACCCGGGCCCGCCCTGCCCGCCGTGCGCCTCAG CCCGCGTCGTCCCCGCCGCCCGCAGGCCCCGGGCCCGGGCCCGCCCTGCCCGCCGTGCGCCTCAG T C DMWD Ensembl:ENSG00000185800 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45791077..45792802 26863410 MeRIP-seq:(Medium) rs1308327495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4537475,Human_RBP_ID_5321750,Human_RBP_ID_9329043,Human_RBP_ID_22533431 69767 RMVar_ID_69767 Human_SNP_ID_667307910 m1A Human chr19 + 45792619 45792619 45792619 TGAGGCGGCACCGGAGTCTGGGCGGAAGCCGGACCCGACCTGCGAGCGGCGCCGTCGCCCGGGAG TGAGGCGGCACCGGAGTCTGGGCGGAAGCCGGCCCCGACCTGCGAGCGGCGCCGTCGCCCGGGAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45792392..45792661 26863196 MeRIP-seq:(Medium) rs895071373 Functional Loss SNV dbSNP153 33..33 33 - - - 69768 RMVar_ID_69768 Human_SNP_ID_667307993 m1A Human chr19 - 45792783 45792783 45792783 GGAGGGGGCCCGGCTGCGGGCGGCAGTCCGGCAGTGGCGGGGCCCGGGGGGCGCCCAAGATGGCG GGAGGGGGCCCGGCTGCGGGCGGCAGTCCGGCGGTGGCGGGGCCCGGGGGGCGCCCAAGATGGCG T C DMWD Ensembl:ENSG00000185800 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:45792702..45792802 26863410 MeRIP-seq:(Medium) rs1344152184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5499795,Human_RBP_ID_9329044 69769 RMVar_ID_69769 Human_SNP_ID_667315003 m1A Human chr19 - 45815550 45815550 45815550 CCGAGGCCAAGGGGAACAGCTGACGGGGCTCGAGGGGGAAAGGGGGTGGGACAGGGACTCGGGGC CCGAGGCCAAGGGGAACAGCTGACGGGGCTCGGGGGGGAAAGGGGGTGGGACAGGGACTCGGGGC T C SYMPK Ensembl:ENSG00000125755 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45815501..45815700 26863196 MeRIP-seq:(Medium) rs1164791055 Functional Loss SNV dbSNP153 33..33 33 - - - 69770 RMVar_ID_69770 Human_SNP_ID_667315087 m1A Human chr19 - 45815694 45815694 45815694 CGGCTGCCCTTTCCTTCCCCGGTCACCAGGAGACGGCAGCGGGCGGGCTGACCTTGAAGGAGGAG CGGCTGCCCTTTCCTTCCCCGGTCACCAGGAGGCGGCAGCGGGCGGGCTGACCTTGAAGGAGGAG T C SYMPK Ensembl:ENSG00000125755 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45815509..45815725 26863196 MeRIP-seq:(Medium) rs1568604038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241490,Human_RBP_ID_4537501,Human_RBP_ID_18165789 Human_Splice_Rec_2021048,Human_Splice_Rec_2021100,Human_Splice_Rec_2021150,Human_Splice_Rec_2021200,Human_Splice_Rec_2021206 69771 RMVar_ID_69771 Human_SNP_ID_667315331 m1A Human chr19 + 45816027 45816027 45816027 GCCTGGCCGGGCCGACGGAGAGGGAGAGGGGGAGGAAGAGGAGGGGGCTCCCACTCCTCCCGGCT GCCTGGCCGGGCCGACGGAGAGGGAGAGGGGGGGGAAGAGGAGGGGGCTCCCACTCCTCCCGGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45815976..45816092 26863196 MeRIP-seq:(Medium) rs1409748062 Functional Loss SNV dbSNP153 33..33 33 - - - 69772 RMVar_ID_69772 Human_SNP_ID_667315336 m1A Human chr19 + 45816033 45816033 45816033 CCGGGCCGACGGAGAGGGAGAGGGGGAGGAAGAGGAGGGGGCTCCCACTCCTCCCGGCTTCAGCT CCGGGCCGACGGAGAGGGAGAGGGGGAGGAAGGGGAGGGGGCTCCCACTCCTCCCGGCTTCAGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45815832..45816200 26863196 MeRIP-seq:(Medium) rs1256893363 Functional Loss SNV dbSNP153 33..33 33 - - - 69773 RMVar_ID_69773 Human_SNP_ID_667316586 m1A Human chr19 - 45819410 45819410 45819410 TGCTTGCTGGCTGGTTCTGGACCTAGGGGACGAAGGAGGGGGCCTGGTCAAGGGAGGAGGTCAGG TGCTTGCTGGCTGGTTCTGGACCTAGGGGACGGAGGAGGGGGCCTGGTCAAGGGAGGAGGTCAGG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45819401..45819502 26863196 MeRIP-seq:(Medium) rs1207458994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6774008,Human_RBP_ID_18945676,Human_RBP_ID_26785825 RMVar_hsa_circ_77690,RMVar_hsa_circ_117188,RMVar_hsa_circ_266027,RMVar_hsa_circ_120935,RMVar_hsa_circ_195416,RMVar_hsa_circ_195417,RMVar_hsa_circ_126711,RMVar_hsa_circ_195419,RMVar_hsa_circ_76215,RMVar_hsa_circ_195420,RMVar_hsa_circ_195418 69774 RMVar_ID_69774 Human_SNP_ID_667319213 m1A Human chr19 + 45827873 45827873 45827873 TCCTCGCAGTACTTGCGGACCACCTCCAGGGCACTCTCTGTGATGAGTGGCGCCTCCAGCACAAC TCCTCGCAGTACTTGCGGACCACCTCCAGGGCGCTCTCTGTGATGAGTGGCGCCTCCAGCACAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45823376..45827946 32194978 MeRIP-seq:(Medium) rs1329686722 Functional Loss SNV dbSNP153 33..33 33 - - - 69775 RMVar_ID_69775 Human_SNP_ID_667323985 m1A Human chr19 - 45844112 45844112 45844112 CACCCTGCCATCTCCTCCATCAACCTGACCACAGCGCTGGGCTCCCTTGCCAATATCGCCCGCCA CACCCTGCCATCTCCTCCATCAACCTGACCACGGCGCTGGGCTCCCTTGCCAATATCGCCCGCCA T C SYMPK Ensembl:ENSG00000125755 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45843993..45844243 26863196 MeRIP-seq:(Medium) rs754979365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53584,Human_RBP_ID_911608,Human_RBP_ID_3957193,Human_RBP_ID_4537585,Human_RBP_ID_5527057,Human_RBP_ID_18736016,Human_RBP_ID_26817713 Human_Splice_Rec_2021062,Human_Splice_Rec_2021063,Human_Splice_Rec_2021114,Human_Splice_Rec_2021115,Human_Splice_Rec_2021162,Human_Splice_Rec_2021163,Human_Splice_Rec_2021238,Human_Splice_Rec_2021239,Human_Splice_Rec_2021278,Human_Splice_Rec_2021279,Human_Splice_Rec_2021320,Human_Splice_Rec_2021321 RMVar_hsa_circ_17713,RMVar_hsa_circ_76215,RMVar_hsa_circ_195420,RMVar_hsa_circ_346786,RMVar_hsa_circ_127715,RMVar_hsa_circ_79946,RMVar_hsa_circ_195422,RMVar_hsa_circ_105011,RMVar_hsa_circ_195423,RMVar_hsa_circ_195424,RMVar_hsa_circ_265536,RMVar_hsa_circ_76710,RMVar_hsa_circ_195428,RMVar_hsa_circ_195425,RMVar_hsa_circ_93866,RMVar_hsa_circ_331450,RMVar_hsa_circ_97851,RMVar_hsa_circ_127944,RMVar_hsa_circ_195426,RMVar_hsa_circ_195427,RMVar_hsa_circ_112383,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_335784,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_284439,RMVar_hsa_circ_195438,RMVar_hsa_circ_273156,RMVar_hsa_circ_195437,RMVar_hsa_circ_308553,RMVar_hsa_circ_195439 69776 RMVar_ID_69776 Human_SNP_ID_667324000 m1A Human chr19 - 45844185 45844185 45844185 TCCTCTCTGTCTCTTAGACGTGCTATGGGAAGAGGGCAAGGCAGCCTTGGAGCAGCTGCTTAAGT TCCTCTCTGTCTCTTAGACGTGCTATGGGAAGCGGGCAAGGCAGCCTTGGAGCAGCTGCTTAAGT T G SYMPK Ensembl:ENSG00000125755 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45844069..45848768 32194978 MeRIP-seq:(Medium) rs1243385488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825997,Human_RBP_ID_911609,Human_RBP_ID_5527058,Human_RBP_ID_6774047,Human_RBP_ID_17928049,Human_RBP_ID_22546151,Human_RBP_ID_26817713 Human_Splice_Rec_2021062,Human_Splice_Rec_2021114,Human_Splice_Rec_2021162,Human_Splice_Rec_2021238,Human_Splice_Rec_2021278,Human_Splice_Rec_2021320 RMVar_hsa_circ_17713,RMVar_hsa_circ_76215,RMVar_hsa_circ_195420,RMVar_hsa_circ_346786,RMVar_hsa_circ_127715,RMVar_hsa_circ_79946,RMVar_hsa_circ_195422,RMVar_hsa_circ_105011,RMVar_hsa_circ_195423,RMVar_hsa_circ_195424,RMVar_hsa_circ_265536,RMVar_hsa_circ_76710,RMVar_hsa_circ_195428,RMVar_hsa_circ_195425,RMVar_hsa_circ_93866,RMVar_hsa_circ_331450,RMVar_hsa_circ_97851,RMVar_hsa_circ_127944,RMVar_hsa_circ_195426,RMVar_hsa_circ_195427,RMVar_hsa_circ_112383,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_335784,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_284439,RMVar_hsa_circ_195438,RMVar_hsa_circ_273156,RMVar_hsa_circ_195437,RMVar_hsa_circ_308553,RMVar_hsa_circ_195439 69777 RMVar_ID_69777 Human_SNP_ID_667324996 m1A Human chr19 - 45847802 45847802 45847802 GGCTGACTCAGAGATACCCCGACGCCAGGAGCATGATATCAGCCTGGACCGCATCCCTCGTGACC GGCTGACTCAGAGATACCCCGACGCCAGGAGCGTGATATCAGCCTGGACCGCATCCCTCGTGACC T C SYMPK Ensembl:ENSG00000125755 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45847702..45847865 26863196 MeRIP-seq:(Medium) rs764047353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1890169,Human_RBP_ID_6774053,Human_RBP_ID_8835542,Human_RBP_ID_17928054,Human_RBP_ID_18736017,Human_RBP_ID_26817714 Human_Splice_Rec_2021061,Human_Splice_Rec_2021113,Human_Splice_Rec_2021161,Human_Splice_Rec_2021237,Human_Splice_Rec_2021277,Human_Splice_Rec_2021319 Human_miRNA_ID_2069003 RMVar_hsa_circ_17713,RMVar_hsa_circ_76215,RMVar_hsa_circ_195420,RMVar_hsa_circ_346786,RMVar_hsa_circ_127715,RMVar_hsa_circ_79946,RMVar_hsa_circ_195422,RMVar_hsa_circ_105011,RMVar_hsa_circ_195423,RMVar_hsa_circ_195424,RMVar_hsa_circ_265536,RMVar_hsa_circ_76710,RMVar_hsa_circ_195425,RMVar_hsa_circ_93866,RMVar_hsa_circ_331450,RMVar_hsa_circ_127944,RMVar_hsa_circ_195426,RMVar_hsa_circ_195427,RMVar_hsa_circ_112383,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_195438,RMVar_hsa_circ_308553,RMVar_hsa_circ_69386,RMVar_hsa_circ_344501 69778 RMVar_ID_69778 Human_SNP_ID_667329308 m1A Human chr19 + 45862533 45862533 45862533 CGGTCATAGACATCATAAAACAGCACACAGATAAGAGTCGGATAACAAATTAGACCACACGTGAC CGGTCATAGACATCATAAAACAGCACACAGATTAGAGTCGGATAACAAATTAGACCACACGTGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45862531..45862753 26863196 MeRIP-seq:(Medium) rs1463618670 Functional Loss SNV dbSNP153 33..33 33 - - - 69779 RMVar_ID_69779 Human_SNP_ID_667329313 m1A Human chr19 + 45862542 45862542 45862542 ACATCATAAAACAGCACACAGATAAGAGTCGGATAACAAATTAGACCACACGTGACATGAAGGAA ACATCATAAAACAGCACACAGATAAGAGTCGGGTAACAAATTAGACCACACGTGACATGAAGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45862538..45862671 26863196 MeRIP-seq:(Medium) rs375473786 Functional Loss SNV dbSNP153 33..33 33 - - - 69780 RMVar_ID_69780 Human_SNP_ID_667335540 m1A Human chr19 - 45884393 45884393 45884393 GGGCGCCAGCCCTGCAGCCTCCTCCACGGCCCAGCCGCCAACCCAGCATCGCCTTGTGGCCCGCA GGGCGCCAGCCCTGCAGCCTCCTCCACGGCCCGGCCGCCAACCCAGCATCGCCTTGTGGCCCGCA T C IRF2BP1 Ensembl:ENSG00000170604 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:45884344..45884752;chr19:45884348..45884850 26863196 MeRIP-seq:(Medium) rs1304483319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908782,Human_RBP_ID_22448848 69781 RMVar_ID_69781 Human_SNP_ID_667335683 m1A Human chr19 + 45884698 45884698 45884698 GGGGCTCGCGGGGGTGGGCCACAGAGAGCCGCAGGGGCCGGCTCTGGGTACTGCTGGGGCAGGGC GGGGCTCGCGGGGGTGGGCCACAGAGAGCCGCGGGGGCCGGCTCTGGGTACTGCTGGGGCAGGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45884526..45884800 26863410 MeRIP-seq:(Medium) rs1429195751 Functional Loss SNV dbSNP153 33..33 33 - - - 69782 RMVar_ID_69782 Human_SNP_ID_667335768 m1A Human chr19 + 45884989 45884989 45884989 TTCAGCTCGAACTCGTATCCTGGAGGACGGGCAGTAGCATCGAAGGCGAACACTCGCCCCACCAG TTCAGCTCGAACTCGTATCCTGGAGGACGGGCGGTAGCATCGAAGGCGAACACTCGCCCCACCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45883754..45885135 32194978 MeRIP-seq:(Medium) rs375045022 Functional Loss SNV dbSNP153 33..33 33 - - - 69783 RMVar_ID_69783 Human_SNP_ID_667335962 m1A Human chr19 - 45885482 45885482 45885482 GCCCCAGCTGCCGCCCCCGCAGGCCCAGCCCCAGCCGTCAGGGACCGGCGGCGGCGTGTCGGGCC GCCCCAGCTGCCGCCCCCGCAGGCCCAGCCCCCGCCGTCAGGGACCGGCGGCGGCGTGTCGGGCC T G IRF2BP1 Ensembl:ENSG00000170604 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45885433..45885609 26863196 MeRIP-seq:(Medium) rs971089723 Functional Loss SNV dbSNP153 33..33 33 - - - 69784 RMVar_ID_69784 Human_SNP_ID_667335988 m1A Human chr19 - 45885526 45885526 45885526 AAGCACCCGGCCACCAAGGACCTGGCGGCGGCAGCCGCACAGGGGCCCCAGCTGCCGCCCCCGCA AAGCACCCGGCCACCAAGGACCTGGCGGCGGCGGCCGCACAGGGGCCCCAGCTGCCGCCCCCGCA T C IRF2BP1 Ensembl:ENSG00000170604 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr19:45885426..45885591;chr19:45885479..45885776 26863410,32194978 MeRIP-seq:(Medium) rs953214372 Functional Loss SNV dbSNP153 33..33 33 - - - 69785 RMVar_ID_69785 Human_SNP_ID_667336102 m1A Human chr19 + 45885841 45885821 45885841 CCACCGGCCGCCGACGTGCGATCCGCGCCGCCAACGTTCGATCCGCGTCCCGGGGACAGCGCGAG CCACCGGCCGCCG____________________ACGTTCGATCCGCGTCCCGGGGACAGCGCGAG GACGTGCGATCCGCGCCGCCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45885676..45886100 26863410 MeRIP-seq:(Medium) rs754027510 Functional Loss DEL dbSNP153 14..33 33 - - - 69786 RMVar_ID_69786 Human_SNP_ID_667336127 m1A Human chr19 - 45885899 45885899 45885899 GGGAAGGGGGGCCGGGCCTGGATCCGGCGGGGAGGCCGAGCCGGAGGCCGGACCGTGGCTCGCGC GGGAAGGGGGGCCGGGCCTGGATCCGGCGGGGGGGCCGAGCCGGAGGCCGGACCGTGGCTCGCGC T C IRF2BP1 Ensembl:ENSG00000170604 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:45885851..45886087 26863196 MeRIP-seq:(Medium) rs1295171927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241836,Human_RBP_ID_908783,Human_RBP_ID_4557606,Human_RBP_ID_5238825,Human_RBP_ID_5527060,Human_RBP_ID_8942225,Human_RBP_ID_9329046,Human_RBP_ID_22071249,Human_RBP_ID_22448849,Human_RBP_ID_22720159,Human_RBP_ID_26992011 69787 RMVar_ID_69787 Human_SNP_ID_667337867 m1A Human chr19 - 45891214 45891214 45891214 GGCTGCCCACGGCCCAAGGAGCGTGAGTCACCACCCCCTTCGGCCCTGCAGCCGGTCCAGCTGCC GGCTGCCCACGGCCCAAGGAGCGTGAGTCACCCCCCCCTTCGGCCCTGCAGCCGGTCCAGCTGCC T G MYPOP Ensembl:ENSG00000176182 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45891164..45891230 26863196 MeRIP-seq:(Medium) rs1568641470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91019,RMVar_hsa_circ_195449 69788 RMVar_ID_69788 Human_SNP_ID_667339131 m1A Human chr19 - 45895506 45895506 45895506 GCCAGGTGGAGATAAGTGCTGGGAGAGGAATCAGGTAGGGTTAGGGGAGAAAAAAAGAAGGAGAT GCCAGGTGGAGATAAGTGCTGGGAGAGGAATCGGGTAGGGTTAGGGGAGAAAAAAAGAAGGAGAT T C MYPOP Ensembl:ENSG00000176182 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:45895500..45895596;chr19:45895498..45895586 26863196 MeRIP-seq:(Medium) rs977249362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6774229 RMVar_hsa_circ_91019,RMVar_hsa_circ_195449 69789 RMVar_ID_69789 Human_SNP_ID_667340824 m1A Human chr19 - 45901457 45901457 45901457 GCACTCCACGCAGGGCGCCGGGCCCGCCGCGGAGGACGCTTTCTCCGCGGAAGAGGAGACCATTT GCACTCCACGCAGGGCGCCGGGCCCGCCGCGGTGGACGCTTTCTCCGCGGAAGAGGAGACCATTT T A MYPOP Ensembl:ENSG00000176182 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45901412..45901711 32194978 MeRIP-seq:(Medium) rs1568645918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908785 RMVar_hsa_circ_91019,RMVar_hsa_circ_195449 69790 RMVar_ID_69790 Human_SNP_ID_667340961 m1A Human chr19 - 45901811 45901811 45901811 TGCGCCCTTTGCCCGCAGCGCCGGCGCCCCCCATGCGCCAGACGGCAGGACGGCGGCGTCGGGGG TGCGCCCTTTGCCCGCAGCGCCGGCGCCCCCCCTGCGCCAGACGGCAGGACGGCGGCGTCGGGGG T G MYPOP Ensembl:ENSG00000176182 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45901760..45902604 26863196 MeRIP-seq:(Medium) rs1392543616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907891,Human_RBP_ID_5376995,Human_RBP_ID_18998227,Human_RBP_ID_19090467,Human_RBP_ID_23257802,Human_RBP_ID_26785832 Human_Splice_Rec_2021388 RMVar_hsa_circ_91019,RMVar_hsa_circ_195449 69791 RMVar_ID_69791 Human_SNP_ID_667341152 m1A Human chr19 - 45902479 45902479 45902479 GTCCCCCGTAGCCTCCGTTGTCTCCTTGTGATACGGGACCCCCGTTATTTCCAGAGCTCCCCTTA GTCCCCCGTAGCCTCCGTTGTCTCCTTGTGATGCGGGACCCCCGTTATTTCCAGAGCTCCCCTTA T C MYPOP Ensembl:ENSG00000176182 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:45902458..45902590 26863196 MeRIP-seq:(Medium) rs1199003025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907892,Human_RBP_ID_19090468 69792 RMVar_ID_69792 Human_SNP_ID_667360258 m1A Human chr19 - 45973485 45973467 45973485 GCACGGCCTCTTCACGGCCTCCGCGGCCCCGCAGCCGCCGCCGCCCCCGCCGCCGCCGCCGCCGC GCACGGCCTCTTCACGGCCTCCGCGGCCCCGC__________________CGCCGCCGCCGCCGC GGCGGGGGCGGCGGCGGCT G NOVA2 Ensembl:ENSG00000104967 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr19:45973376..45973562;chr19:45973480..45973559 26863196 MeRIP-seq:(Medium) rs1331009378 Functional Loss DEL dbSNP153 33..50 33 - - - 69793 RMVar_ID_69793 Human_SNP_ID_667360262 m1A Human chr19 - 45973485 45973485 45973485 GCACGGCCTCTTCACGGCCTCCGCGGCCCCGCAGCCGCCGCCGCCCCCGCCGCCGCCGCCGCCGC GCACGGCCTCTTCACGGCCTCCGCGGCCCCGCCGCCGCCGCCGCCCCCGCCGCCGCCGCCGCCGC T G NOVA2 Ensembl:ENSG00000104967 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr19:45973376..45973562;chr19:45973480..45973559 26863196 MeRIP-seq:(Medium) rs1162019576 Functional Loss SNV dbSNP153 33..33 33 - - - 69794 RMVar_ID_69794 Human_SNP_ID_667360298 m1A Human chr19 + 45973587 45973577 45973587 GCGGGGGGCGGGGGGCGGGGGAGGGGGAGGGGAGGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG GCGGGGGGCGGGGGGCGGGGGAG__________GGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG GGGGGAGGGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45973366..45973588 26863196 MeRIP-seq:(Medium) rs1224398894 Functional Loss DEL dbSNP153 24..33 33 - - - 69795 RMVar_ID_69795 Human_SNP_ID_667360299 m1A Human chr19 + 45973587 45973577 45973587 GCGGGGGGCGGGGGGCGGGGGAGGGGGAGGGGAGGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG GCGGGGGGCGGGGGGCGGGGGAGGGGGA_____GGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG GGGGGAGGGGA GGGGGA - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45973366..45973588 26863196 MeRIP-seq:(Medium) rs1224398894 Functional Loss DEL dbSNP153 29..33 33 - - - 69796 RMVar_ID_69796 Human_SNP_ID_667360304 m1A Human chr19 + 45973587 45973587 45973587 GCGGGGGGCGGGGGGCGGGGGAGGGGGAGGGGAGGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG GCGGGGGGCGGGGGGCGGGGGAGGGGGAGGGGGGGGGAGGTGGGAGGGGGAGGGGGCGGTGGAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:45973366..45973588 26863196 MeRIP-seq:(Medium) rs1354750666 Functional Loss SNV dbSNP153 33..33 33 - - - 69797 RMVar_ID_69797 Human_SNP_ID_667360419 m1A Human chr19 - 45973886 45973886 45973886 CTCCCACTCCGGCCACGCTCCTCCGGCCCCCCACCCCGAGCAGGGTCTGGGGGGCTCGGCCCTCT CTCCCACTCCGGCCACGCTCCTCCGGCCCCCCCCCCCGAGCAGGGTCTGGGGGGCTCGGCCCTCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45973881..45973976 26863196 MeRIP-seq:(Medium) rs1468360688 Functional Loss SNV dbSNP153 33..33 33 - - - 69798 RMVar_ID_69798 Human_SNP_ID_667367413 m1A Human chr19 - 45999381 45999381 45999381 GGCCTGGCCTGGATGACCCCCTTCCCGACCCCATTCTGACCTCACCTCCCCACCACGTGGGTGAA GGCCTGGCCTGGATGACCCCCTTCCCGACCCCCTTCTGACCTCACCTCCCCACCACGTGGGTGAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45999375..46000164 26863196 MeRIP-seq:(Medium) rs1413183861 Functional Loss SNV dbSNP153 33..33 33 - - - 69799 RMVar_ID_69799 Human_SNP_ID_667367417 m1A Human chr19 + 45999392 45999392 45999392 GGTGGGGAGGTGAGGTCAGAATGGGGTCGGGAAGGGGGTCATCCAGGCCAGGCCACGCGTGTGAA GGTGGGGAGGTGAGGTCAGAATGGGGTCGGGAGGGGGGTCATCCAGGCCAGGCCACGCGTGTGAA A G CCDC61 Ensembl:ENSG00000104983 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45999389..45999601 26863196 MeRIP-seq:(Medium) rs1377371131 Functional Loss SNV dbSNP153 33..33 33 - - - 69800 RMVar_ID_69800 Human_SNP_ID_667367486 m1A Human chr19 - 45999667 45999667 45999667 CCTGGCTCCACCTTCCAAATGGCTCTCCCCAGATAGCTCACAGATTTCACAGCTCTTACCCCGGG CCTGGCTCCACCTTCCAAATGGCTCTCCCCAGCTAGCTCACAGATTTCACAGCTCTTACCCCGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:45999665..46000089;chr19:45999665..46000160 26863196 MeRIP-seq:(Medium) rs1239986346 Functional Loss SNV dbSNP153 33..33 33 - - - 69801 RMVar_ID_69801 Human_SNP_ID_667367620 m1A Human chr19 - 46000241 46000241 46000241 CCATATTTCACCTGGATTCTGTTCCCTCCCAAATTGCTTGTAACCCCACCCCCAACCCCCACTCC CCATATTTCACCTGGATTCTGTTCCCTCCCAATTTGCTTGTAACCCCACCCCCAACCCCCACTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46000236..46000825 26863196 MeRIP-seq:(Medium) rs1568686412 Functional Loss SNV dbSNP153 33..33 33 - - - 69802 RMVar_ID_69802 Human_SNP_ID_667371689 m1A Human chr19 + 46015147 46015147 46015147 GCTGGCCGGGCGCGCGGCACGCCAGGAGGCCGAGGCGCTGCGCGGGCTGGTGCGCGGGCTGGAGC GCTGGCCGGGCGCGCGGCACGCCAGGAGGCCGGGGCGCTGCGCGGGCTGGTGCGCGGGCTGGAGC A G CCDC61 Ensembl:ENSG00000104983 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46006499..46016069 26863196 MeRIP-seq:(Medium) rs1483828805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22977772 Human_Splice_Rec_2021434,Human_Splice_Rec_2021464,Human_Splice_Rec_2021474 RMVar_hsa_circ_94330,RMVar_hsa_circ_124279,RMVar_hsa_circ_195452,RMVar_hsa_circ_195454 69803 RMVar_ID_69803 Human_SNP_ID_667403317 m1A Human chr19 - 46148270 46148270 46148270 CTTACCGAAGATTCTGGGCACCATGGAGCTTCAGAGCAGCTGATGGGACAGCAGCAGTGCAAATG CTTACCGAAGATTCTGGGCACCATGGAGCTTCGGAGCAGCTGATGGGACAGCAGCAGTGCAAATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46148258..46148323 26863196 MeRIP-seq:(Medium) rs1001640909 Functional Loss SNV dbSNP153 33..33 33 - - - 69804 RMVar_ID_69804 Human_SNP_ID_667415800 m1A Human chr19 + 46196432 46196431 46196432 AATTCCCCATCCACAGCCCCTGGGTCAGCCCCATCCACAGCTGTTTCAGTCCCCAAACTACTCCC AATTCCCCATCCACAGCCCCTGGGTCAGCCCC_TCCACAGCTGTTTCAGTCCCCAAACTACTCCC CA C IGFL1P1 Ensembl:ENSG00000268879 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:46196387..46196519 26863196 MeRIP-seq:(Medium) rs1568459535 Functional Loss DEL dbSNP153 33..33 33 - - - 69805 RMVar_ID_69805 Human_SNP_ID_667415801 m1A Human chr19 + 46196432 46196432 46196432 AATTCCCCATCCACAGCCCCTGGGTCAGCCCCATCCACAGCTGTTTCAGTCCCCAAACTACTCCC AATTCCCCATCCACAGCCCCTGGGTCAGCCCCTTCCACAGCTGTTTCAGTCCCCAAACTACTCCC A T IGFL1P1 Ensembl:ENSG00000268879 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:46196387..46196519 26863196 MeRIP-seq:(Medium) rs1479485347 Functional Loss SNV dbSNP153 33..33 33 - - - 69806 RMVar_ID_69806 Human_SNP_ID_667415814 m1A Human chr19 + 46196478 46196478 46196478 CAGTCCCCAAACTACTCCCCAAACTTATGCCTAGCCCTGGTTCCAGTCCCACCCAGTCTTTTTCT CAGTCCCCAAACTACTCCCCAAACTTATGCCTGGCCCTGGTTCCAGTCCCACCCAGTCTTTTTCT A G IGFL1P1 Ensembl:ENSG00000268879 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:46196051..46197607;chr19:46196326..46196935 26863196 MeRIP-seq:(Medium) rs1298779161 Functional Loss SNV dbSNP153 33..33 33 - - - 69807 RMVar_ID_69807 Human_SNP_ID_667416171 m1A Human chr19 - 46197868 46197868 46197868 GGGCAACATGACAAAACCCCATCTGTGATGGGAGGAGGGCAGCCAGGGCCAGTCCAGGGCTCCTG GGGCAACATGACAAAACCCCATCTGTGATGGGGGGAGGGCAGCCAGGGCCAGTCCAGGGCTCCTG T C IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46197858..46197926 26863196 MeRIP-seq:(Medium) rs1004937626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5321760 RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 69808 RMVar_ID_69808 Human_SNP_ID_667416288 m1A Human chr19 - 46198066 46198066 46198066 AAAGGAAAAAGAAAGGAAGGAAGGAAGGAAGGAAGGAAAGGAAGGAAGGAAGGCAGGAAGGAAGG AAAGGAAAAAGAAAGGAAGGAAGGAAGGAAGGCAGGAAAGGAAGGAAGGAAGGCAGGAAGGAAGG T G IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46198058..46198238 26863196 MeRIP-seq:(Medium) rs200217773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 69809 RMVar_ID_69809 Human_SNP_ID_667417310 m1A Human chr19 + 46201914 46201906 46201915 CCAGCCACCTCTCTAAGAGGAAATTGTTGGGCAGGTTGGGGAGGGCTAGTCACGGAACAAAACTG CCAGCCACCTCTCTAAGAGGAAATT_________GTTGGGGAGGGCTAGTCACGGAACAAAACTG TGTTGGGCAG T AC006262.1 Ensembl:ENSG00000268460 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46201911..46202186 26863196 MeRIP-seq:(Medium) rs77448367 Functional Loss DEL dbSNP153 26..34 33 - - - 69810 RMVar_ID_69810 Human_SNP_ID_667417601 m1A Human chr19 + 46203026 46203026 46203026 GAAGAGAGTCCACCAACAGGCTTTGTGTGAGCAACAAGACTGTTTATTTTACTTGGGTGCAACTG GAAGAGAGTCCACCAACAGGCTTTGTGTGAGCGACAAGACTGTTTATTTTACTTGGGTGCAACTG A G AC006262.1 Ensembl:ENSG00000268460 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:46202976..46203025 26863196 MeRIP-seq:(Medium) rs904432898 Functional Loss SNV dbSNP153 33..33 33 - - - 69811 RMVar_ID_69811 Human_SNP_ID_667455495 m1A Human chr19 - 46347132 46347132 46347132 CCATCAGCCGGGGGTTCGTCCCGGGGGGGCTCAGCACACTCAGTCCTCTCGCCCTCCGCCATCGC CCATCAGCCGGGGGTTCGTCCCGGGGGGGCTCGGCACACTCAGTCCTCTCGCCCTCCGCCATCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:46347051..46347631;chr19:46347051..46353800 26863196 MeRIP-seq:(Medium) rs1305738861 Functional Loss SNV dbSNP153 33..33 33 - - - 69812 RMVar_ID_69812 Human_SNP_ID_667455530 m1A Human chr19 - 46347168 46347168 46347168 GCCTGAGTCTTGAGCTCCTCTGCCCGCTTCAGAGCTCCATCAGCCGGGGGTTCGTCCCGGGGGGG GCCTGAGTCTTGAGCTCCTCTGCCCGCTTCAGGGCTCCATCAGCCGGGGGTTCGTCCCGGGGGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:46347118..46347330 26863196 MeRIP-seq:(Medium) rs897464269 Functional Loss SNV dbSNP153 33..33 33 - - - 69813 RMVar_ID_69813 Human_SNP_ID_667456137 m1A Human chr19 + 46349324 46349324 46349324 AAAAAAAAAAGAGAGAAGATGCAGTGTCAGGGAAAGATGGATTTTTTGTAAGGATGGAAGAGAGT AAAAAAAAAAGAGAGAAGATGCAGTGTCAGGGTAAGATGGATTTTTTGTAAGGATGGAAGAGAGT A T PPP5C Ensembl:ENSG00000011485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46349321..46349971 26863196 MeRIP-seq:(Medium) rs1044115664 Functional Loss SNV dbSNP153 33..33 33 - - - 69814 RMVar_ID_69814 Human_SNP_ID_667465081 m1A Human chr19 + 46386024 46386023 46386025 ATTTGCTGGAGGAACAGACACAGGTGTGAGACAAAGAGGGAACGAAAGGGGCCCTCTAGGGTTTT ATTTGCTGGAGGAACAGACACAGGTGTGAGAC__AGAGGGAACGAAAGGGGCCCTCTAGGGTTTT CAA C PPP5C Ensembl:ENSG00000011485 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46386023..46386269 26863196 MeRIP-seq:(Medium) rs1477333325 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_372962,RMVar_hsa_circ_195462 69815 RMVar_ID_69815 Human_SNP_ID_667466558 m1A Human chr19 - 46390677 46390677 46390677 GGGGTCTTCCTATGGCGGGGCCCTATTGCTTGAGTGGGGGAGGAGCCATGCAAATGAGGGGGGCA GGGGTCTTCCTATGGCGGGGCCCTATTGCTTGCGTGGGGGAGGAGCCATGCAAATGAGGGGGGCA T G AC007193.3 Ensembl:ENSG00000269151 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46390626..46390797 26863196 MeRIP-seq:(Medium) rs565833531 Functional Loss SNV dbSNP153 33..33 33 - - - 69816 RMVar_ID_69816 Human_SNP_ID_667473460 m1A Human chr19 - 46412050 46412050 46412050 CAGCCCGGGGGATCGCTTGGGAAACGCGGGAGATGTTTGTGTGCCCCAGGCTTCCCCTAGGCGAT CAGCCCGGGGGATCGCTTGGGAAACGCGGGAGGTGTTTGTGTGCCCCAGGCTTCCCCTAGGCGAT T C CCDC8 Ensembl:ENSG00000169515 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46412002..46412102 32194978 MeRIP-seq:(Medium) rs1036867782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4538043,Human_RBP_ID_17935440 69817 RMVar_ID_69817 Human_SNP_ID_667524565 m1A Human chr19 - 46601363 46601363 46601363 CCTCCGGCGGCGGCAGCAGCTGCAGCAGTTCCAGCTCCGCCGCGCGTCCGCGCCTCCACACTCAC CCTCCGGCGGCGGCAGCAGCTGCAGCAGTTCCTGCTCCGCCGCGCGTCCGCGCCTCCACACTCAC T A - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:46601281..46601381 26863410 MeRIP-seq:(Medium) rs1476365817 Functional Loss SNV dbSNP153 33..33 33 - - - 69818 RMVar_ID_69818 Human_SNP_ID_667524571 m1A Human chr19 - 46601378 46601375 46601378 ACGGGGATCAAGGTTCCTCCGGCGGCGGCAGCAGCTGCAGCAGTTCCAGCTCCGCCGCGCGTCCG ACGGGGATCAAGGTTCCTCCGGCGGCGGCAGC___TGCAGCAGTTCCAGCTCCGCCGCGCGTCCG AGCT A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:46601276..46601475 26863410 MeRIP-seq:(Medium) rs1036423322 Functional Loss DEL dbSNP153 33..35 33 - - - 69819 RMVar_ID_69819 Human_SNP_ID_667524790 m1A Human chr19 + 46602139 46602139 46602139 TGGGAGGAAGAGCCTGGGGTGGGTGGCAGCGGAGATTAGAAGATACTCTTGAAGGCTTCCGGGAC TGGGAGGAAGAGCCTGGGGTGGGTGGCAGCGGGGATTAGAAGATACTCTTGAAGGCTTCCGGGAC A G CALM3 Ensembl:ENSG00000160014 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:46602133..46602237 26863196 MeRIP-seq:(Medium) rs1009583316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6774738,Human_RBP_ID_8196666,Human_RBP_ID_9427448,Human_RBP_ID_13479536 Human_Splice_Rec_2022269 RMVar_hsa_circ_195469,RMVar_hsa_circ_113380,RMVar_hsa_circ_195470,RMVar_hsa_circ_50046 69820 RMVar_ID_69820 Human_SNP_ID_667526367 m1A Human chr19 - 46608576 46608576 46608576 CCCTGGAGAGGGCTGCTTACCTTGTCAAAGACACGGAACGCCTCTCGGATCTCCTCCTCACTGTC CCCTGGAGAGGGCTGCTTACCTTGTCAAAGACTCGGAACGCCTCTCGGATCTCCTCCTCACTGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:46608476..46608600 26863196 MeRIP-seq:(Medium) rs559783307 Functional Loss SNV dbSNP153 33..33 33 - - - 69821 RMVar_ID_69821 Human_SNP_ID_667526593 m1A Human chr19 - 46609188 46609188 46609188 AGAGAGAGTGCGCGCGCGAGAAGAGAGAGATCAAGAGAACGGGCATCGCCAGCTGCCCGGGGGGC AGAGAGAGTGCGCGCGCGAGAAGAGAGAGATCGAGAGAACGGGCATCGCCAGCTGCCCGGGGGGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:46609150..46609275 26863196 MeRIP-seq:(Medium) rs1357645531 Functional Loss SNV dbSNP153 33..33 33 - - - 69822 RMVar_ID_69822 Human_SNP_ID_667526619 m1A Human chr19 + 46609224 46609224 46609224 CTCTCTCTTCTCGCGCGCGCACTCTCTCTTCAACACTCCCCTGCGTACCCCGGTTCTAGCAAACA CTCTCTCTTCTCGCGCGCGCACTCTCTCTTCAGCACTCCCCTGCGTACCCCGGTTCTAGCAAACA A G CALM3 Ensembl:ENSG00000160014 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:46609201..46609225 26863196 MeRIP-seq:(Medium) rs1457128739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524076,Human_RBP_ID_826055,Human_RBP_ID_1017183,Human_RBP_ID_1190748,Human_RBP_ID_1240087,Human_RBP_ID_3574119,Human_RBP_ID_4538199,Human_RBP_ID_5421669,Human_RBP_ID_6774771,Human_RBP_ID_8097967,Human_RBP_ID_8490596,Human_RBP_ID_9088897,Human_RBP_ID_13479675,Human_RBP_ID_17270010,Human_RBP_ID_17384952,Human_RBP_ID_17500970,Human_RBP_ID_17656263,Human_RBP_ID_17696068,Human_RBP_ID_17928218,Human_RBP_ID_18736229,Human_RBP_ID_22236702,Human_RBP_ID_23801935,Human_RBP_ID_24484562,Human_RBP_ID_26469116,Human_RBP_ID_27276057,Human_RBP_ID_27469428,Human_RBP_ID_27562640 Human_Splice_Rec_2022182,Human_Splice_Rec_2022190,Human_Splice_Rec_2022200,Human_Splice_Rec_2022208,Human_Splice_Rec_2022218,Human_Splice_Rec_2022226,Human_Splice_Rec_2022238,Human_Splice_Rec_2022248,Human_Splice_Rec_2022256,Human_Splice_Rec_2022268,Human_Splice_Rec_2022278,Human_Splice_Rec_2022288,Human_Splice_Rec_2022292 Human_miRNA_ID_95865,Human_miRNA_ID_1961044,Human_miRNA_ID_2977878 RMVar_hsa_circ_37465,RMVar_hsa_circ_195469,RMVar_hsa_circ_113380,RMVar_hsa_circ_105000,RMVar_hsa_circ_195473 69823 RMVar_ID_69823 Human_SNP_ID_667526638 m1A Human chr19 - 46609319 46609317 46609319 CATGGAGAGAGACTCAGGGAAGAAGGAGAAAGAGCAATCATGCAGCTTGGGACAAATCTTTTGTT CATGGAGAGAGACTCAGGGAAGAAGGAGAAAG__CAATCATGCAGCTTGGGACAAATCTTTTGTT GCT G AC093503.2 Ensembl:ENSG00000269292 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46609126..46610421 26863196 MeRIP-seq:(Medium) rs1457014166 Functional Loss DEL dbSNP153 33..34 33 - - - 69824 RMVar_ID_69824 Human_SNP_ID_667526821 m1A Human chr19 - 46609910 46609910 46609910 GTTAGCACCAGGTATTTACAGAACAGCTCGAGAGCGCTTCAGGAACGCGGGCAAGTCCAATTTGC GTTAGCACCAGGTATTTACAGAACAGCTCGAGCGCGCTTCAGGAACGCGGGCAAGTCCAATTTGC T G AC093503.2 Ensembl:ENSG00000269292 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:46609861..46610009 26863196 MeRIP-seq:(Medium) rs540882337 Functional Loss SNV dbSNP153 33..33 33 - - - 69825 RMVar_ID_69825 Human_SNP_ID_667526942 m1A Human chr19 - 46610282 46610282 46610282 CGAGGGAAGAGGCAGGGAAGAGGGCACGGAGCACAGATGTGAGGAAGCGGCGCCAAGTCACCACG CGAGGGAAGAGGCAGGGAAGAGGGCACGGAGCCCAGATGTGAGGAAGCGGCGCCAAGTCACCACG T G AC093503.2 Ensembl:ENSG00000269292 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr19:46610114..46610462;chr19:46610180..46610447 26863196,26863410 MeRIP-seq:(Medium) rs993013464 Functional Loss SNV dbSNP153 33..33 33 - - - 69826 RMVar_ID_69826 Human_SNP_ID_667526947 m1A Human chr19 - 46610301 46610291 46610302 ATGGGGGCAGGCAGGTGGGCGAGGGAAGAGGCAGGGAAGAGGGCACGGAGCACAGATGTGAGGAA ATGGGGGCAGGCAGGTGGGCGAGGGAAGAGG___________GCACGGAGCACAGATGTGAGGAA CCCTCTTCCCTG C AC093503.2 Ensembl:ENSG00000269292 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:46610251..46610300 26863196 MeRIP-seq:(Medium) rs963310110 Functional Loss DEL dbSNP153 32..42 33 - - - 69827 RMVar_ID_69827 Human_SNP_ID_667526952 m1A Human chr19 - 46610305 46610305 46610305 GAGTATGGGGGCAGGCAGGTGGGCGAGGGAAGAGGCAGGGAAGAGGGCACGGAGCACAGATGTGA GAGTATGGGGGCAGGCAGGTGGGCGAGGGAAGGGGCAGGGAAGAGGGCACGGAGCACAGATGTGA T C AC093503.2 Ensembl:ENSG00000269292 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:46610203..46610475 26863410 MeRIP-seq:(Medium) rs1358405369 Functional Loss SNV dbSNP153 33..33 33 - - - 69828 RMVar_ID_69828 Human_SNP_ID_667526977 m1A Human chr19 + 46610409 46610409 46610409 TTCGCCTCTGGGACAAGTAAGTCAATGTGGGCAGTTCAGTCGTCTGGGTTTTTTCCCCTTTTCTG TTCGCCTCTGGGACAAGTAAGTCAATGTGGGCGGTTCAGTCGTCTGGGTTTTTTCCCCTTTTCTG A G CALM3 Ensembl:ENSG00000160014 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46609326..46610725 32194978 MeRIP-seq:(Medium) rs945099633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524112,Human_RBP_ID_1017193,Human_RBP_ID_1190769,Human_RBP_ID_1295099,Human_RBP_ID_1568635,Human_RBP_ID_1890291,Human_RBP_ID_6774822,Human_RBP_ID_13479742,Human_RBP_ID_17270027,Human_RBP_ID_17384969,Human_RBP_ID_17500985,Human_RBP_ID_17928231,Human_RBP_ID_18306354,Human_RBP_ID_18947123,Human_RBP_ID_23801973 Human_miRNA_ID_461797,Human_miRNA_ID_928108 RMVar_hsa_circ_195469,RMVar_hsa_circ_113380,RMVar_hsa_circ_105000,RMVar_hsa_circ_195473 69829 RMVar_ID_69829 Human_SNP_ID_667531207 m1A Human chr19 + 46623705 46623705 46623705 AGAAGGCGGCGCCGCCCGGCTGGGCCCAGCGCATGCGGAGGAAGCACCAGCTGCCGGGGCAGTAC AGAAGGCGGCGCCGCCCGGCTGGGCCCAGCGCTTGCGGAGGAAGCACCAGCTGCCGGGGCAGTAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46623664..46623815 32194978 MeRIP-seq:(Medium) rs561566322 Functional Loss SNV dbSNP153 33..33 33 - - - 69830 RMVar_ID_69830 Human_SNP_ID_667531413 m1A Human chr19 + 46624014 46624014 46624014 GCAGGGAGCTGTTGCGCGCATAGGCCACGAACACGGCCGGGCTCAGGAAGCTGGTGCCCAGCAGG GCAGGGAGCTGTTGCGCGCATAGGCCACGAACCCGGCCGGGCTCAGGAAGCTGGTGCCCAGCAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46623963..46624064 32194978 MeRIP-seq:(Medium) rs1460304596 Functional Loss SNV dbSNP153 33..33 33 - - - 69831 RMVar_ID_69831 Human_SNP_ID_667531414 m1A Human chr19 + 46624014 46624014 46624014 GCAGGGAGCTGTTGCGCGCATAGGCCACGAACACGGCCGGGCTCAGGAAGCTGGTGCCCAGCAGG GCAGGGAGCTGTTGCGCGCATAGGCCACGAACGCGGCCGGGCTCAGGAAGCTGGTGCCCAGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46623963..46624064 32194978 MeRIP-seq:(Medium) rs1460304596 Functional Loss SNV dbSNP153 33..33 33 - - - 69832 RMVar_ID_69832 Human_SNP_ID_667545330 m1A Human chr19 + 46675106 46675103 46675106 GTTTGCGCATCTTCACCTGCAGCAGGTTGTTGATGAGGTCAATGGCTGCACAGGAAAGAGAAACA GTTTGCGCATCTTCACCTGCAGCAGGTTGT___TGAGGTCAATGGCTGCACAGGAAAGAGAAACA TTGA T DACT3-AS1 Ensembl:ENSG00000245598 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46674374..46678368 32194978 MeRIP-seq:(Medium) rs765866985 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8103398 69833 RMVar_ID_69833 Human_SNP_ID_667551293 m1A Human chr19 + 46697251 46697251 46697251 AATAGTGCCGCTTTCTCTGCAGAGATGTTTGAAGAGTCACGTGAACCGCCAGACTTTCCTGCCCA AATAGTGCCGCTTTCTCTGCAGAGATGTTTGAGGAGTCACGTGAACCGCCAGACTTTCCTGCCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46697249..46697377 26863196 MeRIP-seq:(Medium) rs561155581 Functional Loss SNV dbSNP153 33..33 33 - - - 69834 RMVar_ID_69834 Human_SNP_ID_667553172 m1A Human chr19 - 46704171 46704171 46704171 CAAGGGCCTCTTCCGGCAGGGCCTGCAATGCAAAGGTTAGCTGGGCCTGTCGGGGAGGACAGACA CAAGGGCCTCTTCCGGCAGGGCCTGCAATGCAGAGGTTAGCTGGGCCTGTCGGGGAGGACAGACA T C PRKD2 Ensembl:ENSG00000105287 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs751786745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19093751 Human_Splice_Rec_2022347,Human_Splice_Rec_2022397,Human_Splice_Rec_2022433,Human_Splice_Rec_2022473,Human_Splice_Rec_2022545 RMVar_hsa_circ_123336,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484,RMVar_hsa_circ_24491,RMVar_hsa_circ_343379,RMVar_hsa_circ_371396,RMVar_hsa_circ_195489,RMVar_hsa_circ_195491,RMVar_hsa_circ_317531,RMVar_hsa_circ_329620,RMVar_hsa_circ_327876 69835 RMVar_ID_69835 Human_SNP_ID_667555977 m1A Human chr19 - 46714049 46714049 46714049 CCCTGGGAGGGTCACAGTCCGCCCGCTGCTGAAGGCGGCTCTGAGCTTTTCCGTCGCCACATCCC CCCTGGGAGGGTCACAGTCCGCCCGCTGCTGACGGCGGCTCTGAGCTTTTCCGTCGCCACATCCC T G PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46714011..46714109 26863196 MeRIP-seq:(Medium) rs778789166 Functional Loss SNV dbSNP153 33..33 33 - - - 69836 RMVar_ID_69836 Human_SNP_ID_667557473 m1A Human chr19 + 46719625 46719623 46719625 AGGGGACCGAGGGTGCAGGGTAGAACCAAACAAGAGAGTGAAATAAATAGAGGGAAAGAGTGGAG AGGGGACCGAGGGTGCAGGGTAGAACCAAAC__GAGAGTGAAATAAATAGAGGGAAAGAGTGGAG CAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46719575..46719665 26863196 MeRIP-seq:(Medium) rs926488809 Functional Loss DEL dbSNP153 32..33 33 - - - 69837 RMVar_ID_69837 Human_SNP_ID_667557475 m1A Human chr19 + 46719625 46719625 46719625 AGGGGACCGAGGGTGCAGGGTAGAACCAAACAAGAGAGTGAAATAAATAGAGGGAAAGAGTGGAG AGGGGACCGAGGGTGCAGGGTAGAACCAAACAGGAGAGTGAAATAAATAGAGGGAAAGAGTGGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46719575..46719665 26863196 MeRIP-seq:(Medium) rs551646028 Functional Loss SNV dbSNP153 33..33 33 - - - 69838 RMVar_ID_69838 Human_SNP_ID_667559710 m1A Human chr19 - 46726632 46726632 46726632 CCCTGCTGGGTGAGCGGCACCAGGGCGCATGCAGCGTGGTGGACAGAGGCCCCCACAGCTCTCCC CCCTGCTGGGTGAGCGGCACCAGGGCGCATGCCGCGTGGTGGACAGAGGCCCCCACAGCTCTCCC T G STRN4 Ensembl:ENSG00000090372 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46726628..46726695 26863196 MeRIP-seq:(Medium) rs989905426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82942,RMVar_hsa_circ_93181,RMVar_hsa_circ_125207,RMVar_hsa_circ_195495,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195497,RMVar_hsa_circ_195499 69839 RMVar_ID_69839 Human_SNP_ID_667560016 m1A Human chr19 + 46727610 46727606 46727610 GAGGGGAGGGAGGGGCAGAGAGGGCCAGGGAGAGAGAGAATGACAGAGAGAGGCAGAGAAAGAGA GAGGGGAGGGAGGGGCAGAGAGGGCCAGG____GAGAGAATGACAGAGAGAGGCAGAGAAAGAGA GGAGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46727607..46727909 26863196 MeRIP-seq:(Medium) rs1375173283 Functional Loss DEL dbSNP153 30..33 33 - - - 69840 RMVar_ID_69840 Human_SNP_ID_667560158 m1A Human chr19 + 46727959 46727959 46727959 GCGGGCCAGTCACTTTTGGGGGCAGCCCATCCACATCCCGCAGGTCAGCCAGAATGCCTTGGAGT GCGGGCCAGTCACTTTTGGGGGCAGCCCATCCGCATCCCGCAGGTCAGCCAGAATGCCTTGGAGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46727876..46728059 32194978 MeRIP-seq:(Medium) rs751742232 Functional Loss SNV dbSNP153 33..33 33 - - - 69841 RMVar_ID_69841 Human_SNP_ID_667561010 m1A Human chr19 - 46730820 46730820 46730820 CAAAGAGCGCTTGGGCGGCTCAGTGCTGGGGCAGATCCCCTTCCTGCAGAACTGCGAGGACGAAG CAAAGAGCGCTTGGGCGGCTCAGTGCTGGGGCCGATCCCCTTCCTGCAGAACTGCGAGGACGAAG T G STRN4 Ensembl:ENSG00000090372 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46728601..46730923 32194978 MeRIP-seq:(Medium) rs763989883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239363,Human_RBP_ID_279795,Human_RBP_ID_4538444,Human_RBP_ID_9382699,Human_RBP_ID_18998250,Human_RBP_ID_22070345,Human_RBP_ID_24545499,Human_RBP_ID_26336467 Human_Splice_Rec_2022622,Human_Splice_Rec_2022623,Human_Splice_Rec_2022656,Human_Splice_Rec_2022657,Human_Splice_Rec_2022706,Human_Splice_Rec_2022707,Human_Splice_Rec_2022739,Human_Splice_Rec_2022806,Human_Splice_Rec_2022807,Human_Splice_Rec_2022830,Human_Splice_Rec_2022831,Human_Splice_Rec_2022847,Human_Splice_Rec_2022854,Human_Splice_Rec_2022855,Human_Splice_Rec_2022860,Human_Splice_Rec_2022861,Human_Splice_Rec_2022864,Human_Splice_Rec_2022865,Human_Splice_Rec_2022878,Human_Splice_Rec_2022888 Human_miRNA_ID_2152322,Human_miRNA_ID_2385892,Human_miRNA_ID_2420786 RMVar_hsa_circ_82942,RMVar_hsa_circ_93181,RMVar_hsa_circ_125207,RMVar_hsa_circ_195495,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195497,RMVar_hsa_circ_195499,RMVar_hsa_circ_195500,RMVar_hsa_circ_358829,RMVar_hsa_circ_361636 69842 RMVar_ID_69842 Human_SNP_ID_667564895 m1A Human chr19 + 46745192 46745192 46745192 CTCACCTCCATACTGGACATGCCCAACACCCCACACTCCAGTTCAGGGCTCTCTACCTACATCCT CTCACCTCCATACTGGACATGCCCAACACCCCGCACTCCAGTTCAGGGCTCTCTACCTACATCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46745189..46745357 32194978 MeRIP-seq:(Medium) rs916506012 Functional Loss SNV dbSNP153 33..33 33 - - - 69843 RMVar_ID_69843 Human_SNP_ID_667565051 m1A Human chr19 + 46745808 46745808 46745808 GCCTCCCCTCCAGGGCTCGAGTCGCCTCTCTCAGGAGCCCCGCGGCCAGCGTGCTCAGTCCCAGT GCCTCCCCTCCAGGGCTCGAGTCGCCTCTCTCGGGAGCCCCGCGGCCAGCGTGCTCAGTCCCAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46745805..46745955 26863196 MeRIP-seq:(Medium) rs1289110464 Functional Loss SNV dbSNP153 33..33 33 - - - 69844 RMVar_ID_69844 Human_SNP_ID_667565247 m1A Human chr19 + 46746225 46746225 46746225 CGAAGCGCGCCCACTCGTGCTGGATAAAGTGCAGGATCCCCGGCAGGCTCAGGGGCTCCGGGCCC CGAAGCGCGCCCACTCGTGCTGGATAAAGTGCGGGATCCCCGGCAGGCTCAGGGGCTCCGGGCCC A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:46746105..46746293 26863196 MeRIP-seq:(Medium) rs865958356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241887 69845 RMVar_ID_69845 Human_SNP_ID_667565258 m1A Human chr19 - 46746249 46746249 46746249 CGGAGGCAGCCCCGGGCCCACGGCGGGCCCGGAGCCCCTGAGCCTGCCGGGGATCCTGCACTTTA CGGAGGCAGCCCCGGGCCCACGGCGGGCCCGGTGCCCCTGAGCCTGCCGGGGATCCTGCACTTTA T A STRN4 Ensembl:ENSG00000090372 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:46746201..46746400 26863196 MeRIP-seq:(Medium) rs748364500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524213,Human_RBP_ID_4538490,Human_RBP_ID_5238831,Human_RBP_ID_9293823 Human_miRNA_ID_2270553 RMVar_hsa_circ_120653,RMVar_hsa_circ_195499 69846 RMVar_ID_69846 Human_SNP_ID_667565285 m1A Human chr19 + 46746353 46746353 46746353 GGGGCGGAGACCGGGGCCGCCCCAGTGGGGCCAGGGCCCGCGCCTGAGCCGAGCGGACGGCAGGA GGGGCGGAGACCGGGGCCGCCCCAGTGGGGCCGGGGCCCGCGCCTGAGCCGAGCGGACGGCAGGA A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:46746201..46746450;chr19:46746176..46746450 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 69847 RMVar_ID_69847 Human_SNP_ID_667565286 m1A Human chr19 + 46746353 46746353 46746353 GGGGCGGAGACCGGGGCCGCCCCAGTGGGGCCAGGGCCCGCGCCTGAGCCGAGCGGACGGCAGGA GGGGCGGAGACCGGGGCCGCCCCAGTGGGGCCTGGGCCCGCGCCTGAGCCGAGCGGACGGCAGGA A T FKRP Ensembl:ENSG00000181027 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:46746201..46746450;chr19:46746176..46746450 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 69848 RMVar_ID_69848 Human_SNP_ID_667567190 m1A Human chr19 + 46753502 46753502 46753502 GAAAAGAAAAGAAATAAGAGCAGTTTGAGAAAATGTTCAGGGTGACTTAAACATACAGGTTGGGG GAAAAGAAAAGAAATAAGAGCAGTTTGAGAAAGTGTTCAGGGTGACTTAAACATACAGGTTGGGG A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46753497..46753824 26863196 MeRIP-seq:(Medium) rs909649064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13480592 69849 RMVar_ID_69849 Human_SNP_ID_667567795 m1A Human chr19 + 46755460 46755460 46755460 AGCTAGCCCCAGACTTCGGCCCCATGCGGCTCACCCGCTGCCAGGCTGCCCTGGCGGCCGCCATC AGCTAGCCCCAGACTTCGGCCCCATGCGGCTCCCCCGCTGCCAGGCTGCCCTGGCGGCCGCCATC A C FKRP Ensembl:ENSG00000181027 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46755410..46755540 26863196 MeRIP-seq:(Medium) rs778085300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241893,Human_RBP_ID_4538505 Human_Splice_Rec_2022940,Human_Splice_Rec_2022946,Human_Splice_Rec_2022956,Human_Splice_Rec_2022962,Human_Splice_Rec_2022970,Human_Splice_Rec_2022974,Human_Splice_Rec_2022980,Human_Splice_Rec_2023004,Human_Splice_Rec_2023020,Human_Splice_Rec_2023026,Human_Splice_Rec_2023032,Human_Splice_Rec_2023036,Human_Splice_Rec_2023050,Human_Splice_Rec_2023064 69850 RMVar_ID_69850 Human_SNP_ID_667567796 m1A Human chr19 + 46755460 46755460 46755460 AGCTAGCCCCAGACTTCGGCCCCATGCGGCTCACCCGCTGCCAGGCTGCCCTGGCGGCCGCCATC AGCTAGCCCCAGACTTCGGCCCCATGCGGCTCGCCCGCTGCCAGGCTGCCCTGGCGGCCGCCATC A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46755410..46755540 26863196 MeRIP-seq:(Medium) rs778085300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241893,Human_RBP_ID_4538505 Human_Splice_Rec_2022940,Human_Splice_Rec_2022946,Human_Splice_Rec_2022956,Human_Splice_Rec_2022962,Human_Splice_Rec_2022970,Human_Splice_Rec_2022974,Human_Splice_Rec_2022980,Human_Splice_Rec_2023004,Human_Splice_Rec_2023020,Human_Splice_Rec_2023026,Human_Splice_Rec_2023032,Human_Splice_Rec_2023036,Human_Splice_Rec_2023050,Human_Splice_Rec_2023064 69851 RMVar_ID_69851 Human_SNP_ID_667576057 m1A Human chr19 + 46784675 46784675 46784675 GCAGCGAGTGGAAGCTTTGGGGGCCCGCCTGCACGCAAATACAGCCCCTACTCATGCCTCAGCCC GCAGCGAGTGGAAGCTTTGGGGGCCCGCCTGCGCGCAAATACAGCCCCTACTCATGCCTCAGCCC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:46784576..46784759 26863410 MeRIP-seq:(Medium) rs760285134 Functional Loss SNV dbSNP153 33..33 33 - - - 69852 RMVar_ID_69852 Human_SNP_ID_667577009 m1A Human chr19 - 46787927 46787927 46787927 GCCGATCCTCCTCGAGACTCCAAGGGGCTCGCAGCGGCGGAGCCCACCGCCAACGGGGGCCTGGC GCCGATCCTCCTCGAGACTCCAAGGGGCTCGCCGCGGCGGAGCCCACCGCCAACGGGGGCCTGGC T G SLC1A5 Ensembl:ENSG00000105281 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46787879..46788040 26863196 MeRIP-seq:(Medium) rs745577334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826092,Human_RBP_ID_914452,Human_RBP_ID_4538698,Human_RBP_ID_22067676,Human_RBP_ID_22446873,Human_RBP_ID_26992406 Human_miRNA_ID_2874253,Human_miRNA_ID_2982214 RMVar_hsa_circ_90411,RMVar_hsa_circ_195502,RMVar_hsa_circ_99587,RMVar_hsa_circ_195522 69853 RMVar_ID_69853 Human_SNP_ID_667577049 m1A Human chr19 + 46788029 46788029 46788029 GAAGCTGGCTGGGAGCGCTTGGGCTCCTTCCCAGGACCCGACGTTCCTAGGACTGAGTTGAGTAA GAAGCTGGCTGGGAGCGCTTGGGCTCCTTCCCGGGACCCGACGTTCCTAGGACTGAGTTGAGTAA A G AC008622.2 Ensembl:ENSG00000275719 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46787863..46788061 32194978 MeRIP-seq:(Medium) rs558624235 Functional Loss SNV dbSNP153 33..33 33 - - - 69854 RMVar_ID_69854 Human_SNP_ID_667577125 m1A Human chr19 - 46788343 46788343 46788343 CCAGGCGTCCGGGATCTGCGCCACCAGAACCTAGCCTCCTGCAGACCTCCGCCATCTGGGGGCAC CCAGGCGTCCGGGATCTGCGCCACCAGAACCTGGCCTCCTGCAGACCTCCGCCATCTGGGGGCAC T C SLC1A5 Ensembl:ENSG00000105281 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:46788206..46788565 26863196 MeRIP-seq:(Medium) rs935074590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53220,Human_RBP_ID_239673,Human_RBP_ID_914453,Human_RBP_ID_1568787,Human_RBP_ID_4538717,Human_RBP_ID_5321773,Human_RBP_ID_5527064,Human_RBP_ID_8835705,Human_RBP_ID_23802334,Human_RBP_ID_26992411,Human_RBP_ID_27276212,Human_RBP_ID_27469568 RMVar_hsa_circ_90411,RMVar_hsa_circ_195502,RMVar_hsa_circ_99587,RMVar_hsa_circ_195522 69855 RMVar_ID_69855 Human_SNP_ID_667577144 m1A Human chr19 - 46788403 46788403 46788403 TCTGGCATCCCAGCCCTCAGTGTCCAAGACCCAGGCAGCCCGGGTCCCCGCCTCCCGGATCCAGG TCTGGCATCCCAGCCCTCAGTGTCCAAGACCCTGGCAGCCCGGGTCCCCGCCTCCCGGATCCAGG T A SLC1A5 Ensembl:ENSG00000105281 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:46788354..46788503 32194978 MeRIP-seq:(Medium) rs1200388050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239674,Human_RBP_ID_826096,Human_RBP_ID_4538717,Human_RBP_ID_5321773,Human_RBP_ID_8490782,Human_RBP_ID_9329064,Human_RBP_ID_22067681,Human_RBP_ID_22447906,Human_RBP_ID_22533182,Human_RBP_ID_27276212 Human_miRNA_ID_2147428,Human_miRNA_ID_2158132,Human_miRNA_ID_3022555 RMVar_hsa_circ_90411,RMVar_hsa_circ_195502,RMVar_hsa_circ_99587,RMVar_hsa_circ_195522 69856 RMVar_ID_69856 Human_SNP_ID_667583677 m1A Human chr19 - 46810989 46810989 46810989 GGTGGCGCGTGCCTGTAGTCCCAGCTACTCGGAAGGCTGAGGCAGGAGAAGGGCGTGAACCCGGG GGTGGCGCGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAAGGGCGTGAACCCGGG T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1425006041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20405976,Human_RBP_ID_22811416,Human_RBP_ID_27276213 69857 RMVar_ID_69857 Human_SNP_ID_667591423 m1A Human chr19 - 46838239 46838239 46838239 GTGGGCAGAGGCCACCGTGTGTGTCCCGAGTAACCGTGCCGTTGTCGTGTGATGCCATAAGCGTC GTGGGCAGAGGCCACCGTGTGTGTCCCGAGTAGCCGTGCCGTTGTCGTGTGATGCCATAAGCGTC T C AP2S1 Ensembl:ENSG00000042753 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46838176..46838425 32194978 MeRIP-seq:(Medium) rs565674271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137144,Human_RBP_ID_524276,Human_RBP_ID_1190824,Human_RBP_ID_1568799,Human_RBP_ID_1890362,Human_RBP_ID_5116337,Human_RBP_ID_5145327,Human_RBP_ID_8490788,Human_RBP_ID_9088953,Human_RBP_ID_17386901,Human_RBP_ID_17655373,Human_RBP_ID_22503302,Human_RBP_ID_23210992,Human_RBP_ID_23802348 Human_miRNA_ID_1207592 RMVar_hsa_circ_77876,RMVar_hsa_circ_124807,RMVar_hsa_circ_195523,RMVar_hsa_circ_83484,RMVar_hsa_circ_114536,RMVar_hsa_circ_81873,RMVar_hsa_circ_195525,RMVar_hsa_circ_195527,RMVar_hsa_circ_195528,RMVar_hsa_circ_195526,RMVar_hsa_circ_195524 69858 RMVar_ID_69858 Human_SNP_ID_667591428 m1A Human chr19 + 46838254 46838254 46838254 ACACGACAACGGCACGGTTACTCGGGACACACACGGTGGCCTCTGCCCACAGCCAGGGCCCAGAG ACACGACAACGGCACGGTTACTCGGGACACACCCGGTGGCCTCTGCCCACAGCCAGGGCCCAGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46838206..46838550 26863196 MeRIP-seq:(Medium) rs763068463 Functional Loss SNV dbSNP153 33..33 33 - - - 69859 RMVar_ID_69859 Human_SNP_ID_667591434 m1A Human chr19 + 46838270 46838270 46838270 GTTACTCGGGACACACACGGTGGCCTCTGCCCACAGCCAGGGCCCAGAGGCAGTGGGGTGCAGTC GTTACTCGGGACACACACGGTGGCCTCTGCCCTCAGCCAGGGCCCAGAGGCAGTGGGGTGCAGTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46838219..46838525 26863196 MeRIP-seq:(Medium) rs1366869234 Functional Loss SNV dbSNP153 33..33 33 - - - 69860 RMVar_ID_69860 Human_SNP_ID_667594911 m1A Human chr19 + 46850700 46850700 46850700 CGGCAGAGAAGGGACTTGTCAGCGCCCGATCCAGCCTCGGCTATTTACGCGTGGGCCCCCCCTCC CGGCAGAGAAGGGACTTGTCAGCGCCCGATCCGGCCTCGGCTATTTACGCGTGGGCCCCCCCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:46850697..46850850 26863196 MeRIP-seq:(Medium) rs763564428 Functional Loss SNV dbSNP153 33..33 33 - - - 69861 RMVar_ID_69861 Human_SNP_ID_667594946 m1A Human chr19 - 46850753 46850753 46850753 GGTCTGGACGGGGGTCGCCATGGTAACGGGGGAGCGCTACGCCGGGGACTGGCGGAGGGGGGGCC GGTCTGGACGGGGGTCGCCATGGTAACGGGGGGGCGCTACGCCGGGGACTGGCGGAGGGGGGGCC T C AP2S1 Ensembl:ENSG00000042753 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:46850751..46850825;chr19:46850748..46850846 32194978 MeRIP-seq:(Medium) rs772626569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5320485,Human_RBP_ID_8196692 Human_Splice_Rec_2023147 RMVar_hsa_circ_114536,RMVar_hsa_circ_195528 69862 RMVar_ID_69862 Human_SNP_ID_667594968 m1A Human chr19 + 46850788 46850788 46850788 CCCGTTACCATGGCGACCCCCGTCCAGACCCCAGCGGCCCCGGTCCCGCGGCGACTGGGCAGCTC CCCGTTACCATGGCGACCCCCGTCCAGACCCCTGCGGCCCCGGTCCCGCGGCGACTGGGCAGCTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46845976..46850875 26863196 MeRIP-seq:(Medium) rs1377758154 Functional Loss SNV dbSNP153 33..33 33 - - - 69863 RMVar_ID_69863 Human_SNP_ID_667594984 m1A Human chr19 - 46850811 46850811 46850811 CCCTACAACTGCACCCTGAGCCGGAGCTGCCCAGTCGCCGCGGGACCGGGGCCGCTGGGGTCTGG CCCTACAACTGCACCCTGAGCCGGAGCTGCCCCGTCGCCGCGGGACCGGGGCCGCTGGGGTCTGG T G AP2S1 Ensembl:ENSG00000042753 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:46850567..46850850 26863196 MeRIP-seq:(Medium) rs771201476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239052,Human_RBP_ID_524298,Human_RBP_ID_769861,Human_RBP_ID_4557628,Human_RBP_ID_5320485,Human_RBP_ID_9329066,Human_RBP_ID_26816056 Human_Splice_Rec_2023131,Human_Splice_Rec_2023155,Human_Splice_Rec_2023161,Human_Splice_Rec_2023181,Human_Splice_Rec_2023187 RMVar_hsa_circ_114536,RMVar_hsa_circ_195528 69864 RMVar_ID_69864 Human_SNP_ID_667597769 m1A Human chr19 - 46860612 46860612 46860612 CGGCGGCCGCCGTCGCGACTGAGCGCGAGGCGACTTGCAAACGAGCAGAGGGAGCGGGATGGGCG CGGCGGCCGCCGTCGCGACTGAGCGCGAGGCGGCTTGCAAACGAGCAGAGGGAGCGGGATGGGCG T C HSALNG0126726 RNACentral:URS0000EAEE11 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46860192..46860750 26863196 MeRIP-seq:(Medium) rs1191474430 Functional Loss SNV dbSNP153 33..33 33 - - - 69865 RMVar_ID_69865 Human_SNP_ID_667597833 m1A Human chr19 - 46860747 46860747 46860747 GGACAACCAGCGAGGCAGTGGGAAGAGGTCAGAGCGCGTGCGCACCCGAGGGGCTTACTGCCACA GGACAACCAGCGAGGCAGTGGGAAGAGGTCAGGGCGCGTGCGCACCCGAGGGGCTTACTGCCACA T C HSALNG0126726 RNACentral:URS0000EAEE11 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46860169..46860761 26863196 MeRIP-seq:(Medium) rs903688308 Functional Loss SNV dbSNP153 33..33 33 - - - 69866 RMVar_ID_69866 Human_SNP_ID_667598026 m1A Human chr19 + 46861093 46861081 46861093 GAGGGAGGGTCCGCCCGGCCCCCCGCCGCCGGAGCCGCCGCCGCCGCCTCAGCCGCCGCTGGACT GAGGGAGGGTCCGCCCGGCCC____________GCCGCCGCCGCCGCCTCAGCCGCCGCTGGACT CCCCGCCGCCGGA C ARHGAP35 Ensembl:ENSG00000160007 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46861044..46861255 26863196 MeRIP-seq:(Medium) rs1002463112 Functional Loss DEL dbSNP153 22..33 33 - - - 69867 RMVar_ID_69867 Human_SNP_ID_667598043 m1A Human chr19 + 46861093 46861093 46861093 GAGGGAGGGTCCGCCCGGCCCCCCGCCGCCGGAGCCGCCGCCGCCGCCTCAGCCGCCGCTGGACT GAGGGAGGGTCCGCCCGGCCCCCCGCCGCCGGGGCCGCCGCCGCCGCCTCAGCCGCCGCTGGACT A G ARHGAP35 Ensembl:ENSG00000160007 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46861044..46861255 26863196 MeRIP-seq:(Medium) rs999964554 Functional Loss SNV dbSNP153 33..33 33 - - - 69868 RMVar_ID_69868 Human_SNP_ID_667598372 m1A Human chr19 - 46861916 46861909 46861917 GCTCTGCGAGAGGGCAGACAAGAAATGCGGGTAGTAGGGCCCACGAGGGAACGGGATTCAGTCCA GCTCTGCGAGAGGGCAGACAAGAAATGCGGG________CCCACGAGGGAACGGGATTCAGTCCA GCCCTACTA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46861908..46862196 26863196 MeRIP-seq:(Medium) rs1407720916 Functional Loss DEL dbSNP153 32..39 33 - - - 69869 RMVar_ID_69869 Human_SNP_ID_667598375 m1A Human chr19 - 46861916 46861916 46861916 GCTCTGCGAGAGGGCAGACAAGAAATGCGGGTAGTAGGGCCCACGAGGGAACGGGATTCAGTCCA GCTCTGCGAGAGGGCAGACAAGAAATGCGGGTGGTAGGGCCCACGAGGGAACGGGATTCAGTCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46861908..46862196 26863196 MeRIP-seq:(Medium) rs1464610674 Functional Loss SNV dbSNP153 33..33 33 - - - 69870 RMVar_ID_69870 Human_SNP_ID_667612834 m1A Human chr19 - 46918459 46918459 46918459 CTTCCTAGATGGGGGAAAAAAAAAGAAAACCCATCAGCATCATAATTTTAGAACCAAATTTTAAT CTTCCTAGATGGGGGAAAAAAAAAGAAAACCCGTCAGCATCATAATTTTAGAACCAAATTTTAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46918449..46918580 26863196 MeRIP-seq:(Medium) rs144635535 Functional Loss SNV dbSNP153 33..33 33 - - - 69871 RMVar_ID_69871 Human_SNP_ID_667613869 m1A Human chr19 + 46922262 46922262 46922262 CATCCGGAAGAAAGAGGAGGATCAGGCATCCCAGGGTTATAAAGGGGACAATGCTGTCATTCCAT CATCCGGAAGAAAGAGGAGGATCAGGCATCCCCGGGTTATAAAGGGGACAATGCTGTCATTCCAT A C ARHGAP35 Ensembl:ENSG00000160007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46922213..46922278 26863196 MeRIP-seq:(Medium) rs746041884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6775423,Human_RBP_ID_22359063 Human_Splice_Rec_2023191,Human_Splice_Rec_2023201,Human_Splice_Rec_2023211 RMVar_hsa_circ_90622,RMVar_hsa_circ_195532,RMVar_hsa_circ_195533 69872 RMVar_ID_69872 Human_SNP_ID_667613870 m1A Human chr19 + 46922262 46922262 46922262 CATCCGGAAGAAAGAGGAGGATCAGGCATCCCAGGGTTATAAAGGGGACAATGCTGTCATTCCAT CATCCGGAAGAAAGAGGAGGATCAGGCATCCCGGGGTTATAAAGGGGACAATGCTGTCATTCCAT A G ARHGAP35 Ensembl:ENSG00000160007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46922213..46922278 26863196 MeRIP-seq:(Medium) rs746041884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6775423,Human_RBP_ID_22359063 Human_Splice_Rec_2023191,Human_Splice_Rec_2023201,Human_Splice_Rec_2023211 RMVar_hsa_circ_90622,RMVar_hsa_circ_195532,RMVar_hsa_circ_195533 69873 RMVar_ID_69873 Human_SNP_ID_667626725 m1A Human chr19 + 46978705 46978697 46978705 GTTTGTGTGGTGGGATGTGTGTGTGGTGGGGCATGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC GTTTGTGTGGTGGGATGTGTGTGTG________TGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC GGTGGGGCA G ARHGAP35 Ensembl:ENSG00000160007 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46978695..46978760 26863196 MeRIP-seq:(Medium) rs1313666645 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_3583836,Human_RBP_ID_5293018,Human_RBP_ID_5650264,Human_RBP_ID_8103123,Human_RBP_ID_8196695,Human_RBP_ID_8233179,Human_RBP_ID_17272442,Human_RBP_ID_21979318 69874 RMVar_ID_69874 Human_SNP_ID_667626733 m1A Human chr19 + 46978705 46978705 46978705 GTTTGTGTGGTGGGATGTGTGTGTGGTGGGGCATGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC GTTTGTGTGGTGGGATGTGTGTGTGGTGGGGCGTGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC A G ARHGAP35 Ensembl:ENSG00000160007 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46978695..46978760 26863196 MeRIP-seq:(Medium) rs987870909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583836,Human_RBP_ID_5293018,Human_RBP_ID_5650264,Human_RBP_ID_8103123,Human_RBP_ID_8196695,Human_RBP_ID_8233179,Human_RBP_ID_17272442,Human_RBP_ID_21979318 69875 RMVar_ID_69875 Human_SNP_ID_667626879 m1A Human chr19 - 46979061 46979061 46979061 ACACACATCCCACCACACACACCCCACCACACACACACATCCCACCACACACCACACCCCCCCAC ACACACATCCCACCACACACACCCCACCACACCCACACATCCCACCACACACCACACCCCCCCAC T G lnc-TMEM160-1 RNACentral:URS0000D57750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46979050..46979151 26863196 MeRIP-seq:(Medium) rs1460305222 Functional Loss SNV dbSNP153 33..33 33 - - - 69876 RMVar_ID_69876 Human_SNP_ID_667632892 m1A Human chr19 - 47003427 47003427 47003427 TGGCTTTGCACCAAGGGCTGCTGTCCCCTCACACGGTGTCTGCGCTCTCGCTGGGCAGGGGTGGC TGGCTTTGCACCAAGGGCTGCTGTCCCCTCACGCGGTGTCTGCGCTCTCGCTGGGCAGGGGTGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47003377..47003878 32194978 MeRIP-seq:(Medium) rs1268546199 Functional Loss SNV dbSNP153 33..33 33 - - - 69877 RMVar_ID_69877 Human_SNP_ID_667633252 m1A Human chr19 - 47004476 47004476 47004476 TTTTGTTTTTTTCTTAAATGTACACAGGGAACATGATTCTTTTTATGCAAACAATAACTTAGGCC TTTTGTTTTTTTCTTAAATGTACACAGGGAACGTGATTCTTTTTATGCAAACAATAACTTAGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47004426..47004527 32194978 MeRIP-seq:(Medium) rs1244722848 Functional Loss SNV dbSNP153 33..33 33 - - - 69878 RMVar_ID_69878 Human_SNP_ID_667637914 m1A Human chr19 - 47019960 47019960 47019960 GGACCGCCAGTCCGATTACTTGGCCGCAGAGCAGGCTCCGGGCGCGGCGTGGGGCCGGCCGGGCG GGACCGCCAGTCCGATTACTTGGCCGCAGAGCCGGCTCCGGGCGCGGCGTGGGGCCGGCCGGGCG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:47019860..47019975 26863410 MeRIP-seq:(Medium) rs1233839478 Functional Loss SNV dbSNP153 33..33 33 - - - 69879 RMVar_ID_69879 Human_SNP_ID_667642777 m1A Human chr19 - 47036025 47036025 47036025 CGGGCGTCGGCGTCCGCAGCCCCAGTTGCTCCAGCACCTCTGAGTGGTCCCCAGGGTGAATGTAG CGGGCGTCGGCGTCCGCAGCCCCAGTTGCTCCGGCACCTCTGAGTGGTCCCCAGGGTGAATGTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47036011..47036094 26863196 MeRIP-seq:(Medium) rs866514941 Functional Loss SNV dbSNP153 33..33 33 - - - 69880 RMVar_ID_69880 Human_SNP_ID_667644462 m1A Human chr19 - 47040842 47040842 47040842 GTGGGCAGGGAGACGGTGGGGAGAAGAGAAAAAGGTGAAAGCACAGAGAGGCAGAGTCAGAGAGA GTGGGCAGGGAGACGGTGGGGAGAAGAGAAAAGGGTGAAAGCACAGAGAGGCAGAGTCAGAGAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47040804..47040922 26863196 MeRIP-seq:(Medium) rs933623430 Functional Loss SNV dbSNP153 33..33 33 - - - 69881 RMVar_ID_69881 Human_SNP_ID_667645114 m1A Human chr19 + 47042875 47042875 47042875 CTTCCAGCTTCCAGCCAGCGTGGCCTGTGAGGAGGCATCCAGCCCGGGGCCAGAGCCCACAGGTG CTTCCAGCTTCCAGCCAGCGTGGCCTGTGAGGCGGCATCCAGCCCGGGGCCAGAGCCCACAGGTG A C NPAS1 Ensembl:ENSG00000130751 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47041059..47045428 32194978 MeRIP-seq:(Medium) rs567691379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524344 Human_Splice_Rec_2023252,Human_Splice_Rec_2023253,Human_Splice_Rec_2023270,Human_Splice_Rec_2023271,Human_Splice_Rec_2023290,Human_Splice_Rec_2023291,Human_Splice_Rec_2023304,Human_Splice_Rec_2023305,Human_Splice_Rec_2023328 RMVar_hsa_circ_327413,RMVar_hsa_circ_195539 69882 RMVar_ID_69882 Human_SNP_ID_667646275 m1A Human chr19 + 47046220 47046220 47046220 CGCCAGGCCCACGGCGTACGAGGCGCTGCCCCACACCACGCACAGGCCGCCCAGCAGGAAGAAGC CGCCAGGCCCACGGCGTACGAGGCGCTGCCCCCCACCACGCACAGGCCGCCCAGCAGGAAGAAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47045901..47048625 26863196 MeRIP-seq:(Medium) rs768367719 Functional Loss SNV dbSNP153 33..33 33 - - - 69883 RMVar_ID_69883 Human_SNP_ID_667647101 m1A Human chr19 + 47048509 47048509 47048509 CCCGGCGCGGGGACCGTGGCCGGGGGCGAAGGACCCCCGGGCGCCCCCGCTCCGGGGCCGCTGAG CCCGGCGCGGGGACCGTGGCCGGGGGCGAAGGCCCCCCGGGCGCCCCCGCTCCGGGGCCGCTGAG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr19:47048443..47048543;chr19:47048401..47048625;chr19:47048434..47048518 26863410 MeRIP-seq:(Medium) rs936541190 Functional Loss SNV dbSNP153 33..33 33 - - - 69884 RMVar_ID_69884 Human_SNP_ID_667647102 m1A Human chr19 + 47048509 47048509 47048509 CCCGGCGCGGGGACCGTGGCCGGGGGCGAAGGACCCCCGGGCGCCCCCGCTCCGGGGCCGCTGAG CCCGGCGCGGGGACCGTGGCCGGGGGCGAAGGGCCCCCGGGCGCCCCCGCTCCGGGGCCGCTGAG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr19:47048443..47048543;chr19:47048401..47048625;chr19:47048434..47048518 26863410 MeRIP-seq:(Medium) rs936541190 Functional Loss SNV dbSNP153 33..33 33 - - - 69885 RMVar_ID_69885 Human_SNP_ID_667651132 m1A Human chr19 + 47060606 47060606 47060606 CAAAAATTAGCTGGGCATGGTGGTGGGTGCCTATAATCCCAGTCACTAGGGAGGCTGAGGTAGGG CAAAAATTAGCTGGGCATGGTGGTGGGTGCCTCTAATCCCAGTCACTAGGGAGGCTGAGGTAGGG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:47060592..47060676 26863410 MeRIP-seq:(Medium) rs561986783 Functional Loss SNV dbSNP153 33..33 33 - - - 69886 RMVar_ID_69886 Human_SNP_ID_667653178 m1A Human chr19 - 47066661 47066661 47066661 GCAAGTCTGCCCTGGAACAGCCAGAGACAGGGAAGGCCGGTGCTGATGGGGGCACCCCCACGGAC GCAAGTCTGCCCTGGAACAGCCAGAGACAGGGGAGGCCGGTGCTGATGGGGGCACCCCCACGGAC T C ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47066611..47066749 26863196 MeRIP-seq:(Medium) rs1262546526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18736470 RMVar_hsa_circ_107219,RMVar_hsa_circ_111861,RMVar_hsa_circ_195542,RMVar_hsa_circ_195543 69887 RMVar_ID_69887 Human_SNP_ID_667653425 m1A Human chr19 + 47067050 47067050 47067050 TCTGCAGCCGAGGGTCGGTGGGGGCCTTCCGCACCCGGGGGTCACTGGGTTTGTCGCTGGAACCG TCTGCAGCCGAGGGTCGGTGGGGGCCTTCCGCCCCCGGGGGTCACTGGGTTTGTCGCTGGAACCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:47067001..47067350;chr19:47067001..47067325 26863196 MeRIP-seq:(Medium) rs1169335590 Functional Loss SNV dbSNP153 33..33 33 - - - 69888 RMVar_ID_69888 Human_SNP_ID_667653468 m1A Human chr19 - 47067123 47067123 47067123 CCAACCTCCCCGACTTTGAACTTCTGTCTCGCATCCTCAAGACAGTCAATGCCACCGGCTCCTCG CCAACCTCCCCGACTTTGAACTTCTGTCTCGCGTCCTCAAGACAGTCAATGCCACCGGCTCCTCG T C ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47067072..47067376 26863196 MeRIP-seq:(Medium) rs1205584935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5468985,Human_RBP_ID_8835910,Human_RBP_ID_13482396,Human_RBP_ID_26992562,Human_RBP_ID_27276393,Human_RBP_ID_27469746,Human_RBP_ID_27562670 RMVar_hsa_circ_107219,RMVar_hsa_circ_111861,RMVar_hsa_circ_195542,RMVar_hsa_circ_195543 69889 RMVar_ID_69889 Human_SNP_ID_667653587 m1A Human chr19 - 47067329 47067329 47067329 CAAGCCCAGCTTCGCCCGCACCGTGCTCTGGAATCCCGAGGACCTGATCCCCCTACCCATCCCCA CAAGCCCAGCTTCGCCCGCACCGTGCTCTGGACTCCCGAGGACCTGATCCCCCTACCCATCCCCA T G ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47066966..47067394 26863196 MeRIP-seq:(Medium) rs1409909835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8490924,Human_RBP_ID_8835912,Human_RBP_ID_13482397,Human_RBP_ID_18947136,Human_RBP_ID_27469752 RMVar_hsa_circ_107219,RMVar_hsa_circ_111861,RMVar_hsa_circ_195542,RMVar_hsa_circ_195543 69890 RMVar_ID_69890 Human_SNP_ID_667655508 m1A Human chr19 - 47072439 47072439 47072439 GCATGAGCCACTGTCCCCGCAGCAGCTGCAGCAGCAGGACATGTACAACAAGAAGATCCCCTCCT GCATGAGCCACTGTCCCCGCAGCAGCTGCAGCCGCAGGACATGTACAACAAGAAGATCCCCTCCT T G ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47072436..47072636 26863196 MeRIP-seq:(Medium) rs1329477833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5377054 Human_Splice_Rec_2023359,Human_Splice_Rec_2023371 Human_miRNA_ID_1038034,Human_miRNA_ID_1427033,Human_miRNA_ID_1489752,Human_miRNA_ID_2477904,Human_miRNA_ID_2513275,Human_miRNA_ID_2730301,Human_miRNA_ID_3056093 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_108947,RMVar_hsa_circ_84210,RMVar_hsa_circ_269740,RMVar_hsa_circ_195544,RMVar_hsa_circ_328896,RMVar_hsa_circ_106771,RMVar_hsa_circ_195545,RMVar_hsa_circ_195546 69891 RMVar_ID_69891 Human_SNP_ID_667656388 m1A Human chr19 - 47075422 47075422 47075422 AGGAGGGAGATGCAGGGTGGCAGCTGCAGCGCAAGCCATGGCCCCACACACAGTTGAGGAAGGGC AGGAGGGAGATGCAGGGTGGCAGCTGCAGCGCGAGCCATGGCCCCACACACAGTTGAGGAAGGGC T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47075419..47075619 26863196 MeRIP-seq:(Medium) rs1443221679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_108947,RMVar_hsa_circ_84210,RMVar_hsa_circ_269740,RMVar_hsa_circ_195544,RMVar_hsa_circ_106771,RMVar_hsa_circ_195545,RMVar_hsa_circ_195546 69892 RMVar_ID_69892 Human_SNP_ID_667659312 m1A Human chr19 - 47085102 47085102 47085102 AGGCCGAGGTGGCAGCCGAGGAGGGATGAACAAGGGCGGAATGAACGATGACGAAGACTTCTATG AGGCCGAGGTGGCAGCCGAGGAGGGATGAACACGGGCGGAATGAACGATGACGAAGACTTCTATG T G ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47084444..47090224 26863196 MeRIP-seq:(Medium) rs1040680910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54029,Human_RBP_ID_1568900,Human_RBP_ID_1890481,Human_RBP_ID_6775735,Human_RBP_ID_8835949,Human_RBP_ID_9381204,Human_RBP_ID_13482472,Human_RBP_ID_22977774,Human_RBP_ID_26336476 Human_Splice_Rec_2023352,Human_Splice_Rec_2023353,Human_Splice_Rec_2023364,Human_Splice_Rec_2023365,Human_Splice_Rec_2023384 Human_miRNA_ID_1967955 RMVar_hsa_circ_1112,RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_115953,RMVar_hsa_circ_84210,RMVar_hsa_circ_269740,RMVar_hsa_circ_195546,RMVar_hsa_circ_313210,RMVar_hsa_circ_327842,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_24319,RMVar_hsa_circ_70973,RMVar_hsa_circ_195549,RMVar_hsa_circ_195550,RMVar_hsa_circ_339327,RMVar_hsa_circ_49608,RMVar_hsa_circ_195552 69893 RMVar_ID_69893 Human_SNP_ID_667659329 m1A Human chr19 + 47085125 47085125 47085125 ATTCCGCCCTTGTTCATCCCTCCTCGGCTGCCACCTCGGCCTCGGCCCCGACCCATTCCTTTCCC ATTCCGCCCTTGTTCATCCCTCCTCGGCTGCCCCCTCGGCCTCGGCCCCGACCCATTCCTTTCCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47085039..47085375 26863196 MeRIP-seq:(Medium) rs749563659 Functional Loss SNV dbSNP153 33..33 33 - - - 69894 RMVar_ID_69894 Human_SNP_ID_667659330 m1A Human chr19 + 47085125 47085125 47085125 ATTCCGCCCTTGTTCATCCCTCCTCGGCTGCCACCTCGGCCTCGGCCCCGACCCATTCCTTTCCC ATTCCGCCCTTGTTCATCCCTCCTCGGCTGCCGCCTCGGCCTCGGCCCCGACCCATTCCTTTCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47085039..47085375 26863196 MeRIP-seq:(Medium) rs749563659 Functional Loss SNV dbSNP153 33..33 33 - - - 69895 RMVar_ID_69895 Human_SNP_ID_667659352 m1A Human chr19 - 47085175 47085175 47085175 TCCCCTCCACAGGGCTAAGTCGAGGCCGTGGCAGGGGCTCCCGAGGTCGAGGGAAAGGAATGGGT TCCCCTCCACAGGGCTAAGTCGAGGCCGTGGCCGGGGCTCCCGAGGTCGAGGGAAAGGAATGGGT T G ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:47085126..47085425 26863196 MeRIP-seq:(Medium) rs766438167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5374142,Human_RBP_ID_8835951,Human_RBP_ID_9294503,Human_RBP_ID_23802549 Human_Splice_Rec_2023352,Human_Splice_Rec_2023364,Human_Splice_Rec_2023384 RMVar_hsa_circ_1112,RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_115953,RMVar_hsa_circ_84210,RMVar_hsa_circ_269740,RMVar_hsa_circ_195546,RMVar_hsa_circ_313210,RMVar_hsa_circ_327842,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_24319,RMVar_hsa_circ_70973,RMVar_hsa_circ_195549,RMVar_hsa_circ_195550,RMVar_hsa_circ_339327,RMVar_hsa_circ_49608,RMVar_hsa_circ_195552 69896 RMVar_ID_69896 Human_SNP_ID_667661014 m1A Human chr19 - 47090018 47090018 47090018 ACATGGGCAAGGAGGACTATGACGACTTCACCAAAGAGCTGAACCAGTACCGGCGTGCCAAGGAG ACATGGGCAAGGAGGACTATGACGACTTCACCGAAGAGCTGAACCAGTACCGGCGTGCCAAGGAG T C ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47089939..47090124 26863196 MeRIP-seq:(Medium) rs921428613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911659,Human_RBP_ID_5146377,Human_RBP_ID_8835959,Human_RBP_ID_9381206,Human_RBP_ID_17928545,Human_RBP_ID_18995190,Human_RBP_ID_22977775,Human_RBP_ID_26336479,Human_RBP_ID_27815517 Human_Splice_Rec_2023347,Human_Splice_Rec_2023381 Human_miRNA_ID_3108010 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_115953,RMVar_hsa_circ_84210,RMVar_hsa_circ_269740,RMVar_hsa_circ_195546,RMVar_hsa_circ_313210,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_2929,RMVar_hsa_circ_24319,RMVar_hsa_circ_70973,RMVar_hsa_circ_195549,RMVar_hsa_circ_195550,RMVar_hsa_circ_63333,RMVar_hsa_circ_195553,RMVar_hsa_circ_124863,RMVar_hsa_circ_332533 69897 RMVar_ID_69897 Human_SNP_ID_667662417 m1A Human chr19 - 47094480 47094478 47094481 GGGGGAGAAGCATCACAGTGATTCGGATGAGGAGAAGTCCCACAGGAGACTGAAGCGGAAACGGA GGGGGAGAAGCATCACAGTGATTCGGATGAG___AAGTCCCACAGGAGACTGAAGCGGAAACGGA TCTC T ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47094365..47094575 26863196 MeRIP-seq:(Medium) rs748255221 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_54035,Human_RBP_ID_911661,Human_RBP_ID_4539382,Human_RBP_ID_8835964,Human_RBP_ID_9381210,Human_RBP_ID_13482512,Human_RBP_ID_17928548,Human_RBP_ID_18441703,Human_RBP_ID_18532573,Human_RBP_ID_26338031,Human_RBP_ID_27815519 Human_Splice_Rec_2023343,Human_Splice_Rec_2023377,Human_Splice_Rec_2023389,Human_Splice_Rec_2023393 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_2929,RMVar_hsa_circ_70973,RMVar_hsa_circ_195550,RMVar_hsa_circ_63333,RMVar_hsa_circ_40571,RMVar_hsa_circ_195555,RMVar_hsa_circ_345662,RMVar_hsa_circ_105192 69898 RMVar_ID_69898 Human_SNP_ID_667662419 m1A Human chr19 - 47094480 47094480 47094480 GGGGGAGAAGCATCACAGTGATTCGGATGAGGAGAAGTCCCACAGGAGACTGAAGCGGAAACGGA GGGGGAGAAGCATCACAGTGATTCGGATGAGGGGAAGTCCCACAGGAGACTGAAGCGGAAACGGA T C ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47094365..47094575 26863196 MeRIP-seq:(Medium) rs749481873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54035,Human_RBP_ID_911661,Human_RBP_ID_4539382,Human_RBP_ID_8835964,Human_RBP_ID_9381210,Human_RBP_ID_13482512,Human_RBP_ID_17928548,Human_RBP_ID_18441703,Human_RBP_ID_18532573,Human_RBP_ID_26338031,Human_RBP_ID_27815519 Human_Splice_Rec_2023343,Human_Splice_Rec_2023377,Human_Splice_Rec_2023389,Human_Splice_Rec_2023393 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_2929,RMVar_hsa_circ_70973,RMVar_hsa_circ_195550,RMVar_hsa_circ_63333,RMVar_hsa_circ_40571,RMVar_hsa_circ_195555,RMVar_hsa_circ_345662,RMVar_hsa_circ_105192 69899 RMVar_ID_69899 Human_SNP_ID_667662424 m1A Human chr19 - 47094496 47094496 47094496 GAAGCCGGAAAGAAAAGGGGGAGAAGCATCACAGTGATTCGGATGAGGAGAAGTCCCACAGGAGA GAAGCCGGAAAGAAAAGGGGGAGAAGCATCACTGTGATTCGGATGAGGAGAAGTCCCACAGGAGA T A ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47094451..47094608 26863196 MeRIP-seq:(Medium) rs759786004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54035,Human_RBP_ID_4539382,Human_RBP_ID_8835965,Human_RBP_ID_9381210,Human_RBP_ID_13482512,Human_RBP_ID_17928548,Human_RBP_ID_26338031,Human_RBP_ID_27815519 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_2929,RMVar_hsa_circ_70973,RMVar_hsa_circ_195550,RMVar_hsa_circ_63333,RMVar_hsa_circ_40571,RMVar_hsa_circ_195555,RMVar_hsa_circ_345662,RMVar_hsa_circ_105192 69900 RMVar_ID_69900 Human_SNP_ID_667667366 m1A Human chr19 - 47112513 47112513 47112513 GAGTCGCCGCCGCCGCCATCGCCGCCGCCGCCATCAACGCCTTCGCCTCCTCCGTGTTCCCCCGA GAGTCGCCGCCGCCGCCATCGCCGCCGCCGCCGTCAACGCCTTCGCCTCCTCCGTGTTCCCCCGA T C ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47112468..47112667 26863196 MeRIP-seq:(Medium) rs1320998904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2023340,Human_Splice_Rec_2023341 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_195550,RMVar_hsa_circ_195555,RMVar_hsa_circ_105192 69901 RMVar_ID_69901 Human_SNP_ID_667672876 m1A Human chr19 + 47130947 47130947 47130947 AGGAAGAGCCGGCGCCATGGTGGAGAAGGAGGAGGCTGGCGGCGGCATTAGCGAGGAGGAGGCGG AGGAAGAGCCGGCGCCATGGTGGAGAAGGAGGGGGCTGGCGGCGGCATTAGCGAGGAGGAGGCGG A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:47130826..47131108;chr19:47130826..47131482;chr19:47130826..47131630;chr19:47130826..47131406 26863196 MeRIP-seq:(Medium) rs747294644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55425,Human_RBP_ID_4539441,Human_RBP_ID_5116343,Human_RBP_ID_5145332,Human_RBP_ID_5321774,Human_RBP_ID_5443298,Human_RBP_ID_5468990,Human_RBP_ID_5500510,Human_RBP_ID_6775811,Human_RBP_ID_8942227,Human_RBP_ID_9381212,Human_RBP_ID_18995192,Human_RBP_ID_22449543,Human_RBP_ID_22476683,Human_RBP_ID_22978127,Human_RBP_ID_23131557,Human_RBP_ID_23211319,Human_RBP_ID_23802564,Human_RBP_ID_24545732,Human_RBP_ID_26336484,Human_RBP_ID_27815521 Human_Splice_Rec_2023423,Human_Splice_Rec_2023447,Human_Splice_Rec_2023463,Human_Splice_Rec_2023475,Human_Splice_Rec_2023493,Human_Splice_Rec_2023497,Human_Splice_Rec_2023531,Human_Splice_Rec_2023549 69902 RMVar_ID_69902 Human_SNP_ID_667672885 m1A Human chr19 + 47130974 47130974 47130974 GGAGGAGGCTGGCGGCGGCATTAGCGAGGAGGAGGCGGCACAGTATGACCGGCAGATCCGCCTGT GGAGGAGGCTGGCGGCGGCATTAGCGAGGAGGCGGCGGCACAGTATGACCGGCAGATCCGCCTGT A C SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr19:47130876..47131081;chr19:47130878..47131075 26863410 MeRIP-seq:(Medium) rs1371594284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4539441,Human_RBP_ID_5116343,Human_RBP_ID_5145332,Human_RBP_ID_5321775,Human_RBP_ID_8942227,Human_RBP_ID_9381212,Human_RBP_ID_18995192,Human_RBP_ID_22070364,Human_RBP_ID_22448880,Human_RBP_ID_22476683,Human_RBP_ID_22977928,Human_RBP_ID_23211319,Human_RBP_ID_23802564,Human_RBP_ID_24545732,Human_RBP_ID_26336484,Human_RBP_ID_26992602,Human_RBP_ID_27815521 Human_Splice_Rec_2023423,Human_Splice_Rec_2023447,Human_Splice_Rec_2023463,Human_Splice_Rec_2023475,Human_Splice_Rec_2023493,Human_Splice_Rec_2023497,Human_Splice_Rec_2023531,Human_Splice_Rec_2023549 69903 RMVar_ID_69903 Human_SNP_ID_667676382 m1A Human chr19 - 47143480 47143480 47143480 CACCCGAGAGGCCCGCAGCCTGTAAGACAAACATTGTTAACCTGATGATACAGAACAGTGAGCTT CACCCGAGAGGCCCGCAGCCTGTAAGACAAACGTTGTTAACCTGATGATACAGAACAGTGAGCTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:47143476..47143550 26863196 MeRIP-seq:(Medium) rs369007842 Functional Loss SNV dbSNP153 33..33 33 - - - 69904 RMVar_ID_69904 Human_SNP_ID_667676383 m1A Human chr19 - 47143480 47143480 47143480 CACCCGAGAGGCCCGCAGCCTGTAAGACAAACATTGTTAACCTGATGATACAGAACAGTGAGCTT CACCCGAGAGGCCCGCAGCCTGTAAGACAAACCTTGTTAACCTGATGATACAGAACAGTGAGCTT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:47143476..47143550 26863196 MeRIP-seq:(Medium) rs369007842 Functional Loss SNV dbSNP153 33..33 33 - - - 69905 RMVar_ID_69905 Human_SNP_ID_667678183 m1A Human chr19 + 47150299 47150299 47150299 TGAAGCCTCTTTGGAGCGAGCTCAGAATCTCAACCCCATGGTGGATGTGAAGGTGGACACTGAGG TGAAGCCTCTTTGGAGCGAGCTCAGAATCTCAGCCCCATGGTGGATGTGAAGGTGGACACTGAGG A G SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:47150166..47150400;chr19:47150155..47150325 26863196 MeRIP-seq:(Medium) rs1481937544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017310,Human_RBP_ID_1568921,Human_RBP_ID_1890498,Human_RBP_ID_4539459,Human_RBP_ID_6775908,Human_RBP_ID_13483249,Human_RBP_ID_17270119,Human_RBP_ID_17928566,Human_RBP_ID_22448881,Human_RBP_ID_23802611 Human_Splice_Rec_2023400,Human_Splice_Rec_2023401,Human_Splice_Rec_2023412,Human_Splice_Rec_2023413,Human_Splice_Rec_2023418,Human_Splice_Rec_2023419,Human_Splice_Rec_2023426,Human_Splice_Rec_2023427,Human_Splice_Rec_2023440,Human_Splice_Rec_2023441,Human_Splice_Rec_2023450,Human_Splice_Rec_2023451,Human_Splice_Rec_2023466,Human_Splice_Rec_2023467,Human_Splice_Rec_2023478,Human_Splice_Rec_2023479,Human_Splice_Rec_2023494,Human_Splice_Rec_2023495,Human_Splice_Rec_2023500,Human_Splice_Rec_2023501,Human_Splice_Rec_2023518,Human_Splice_Rec_2023519,Human_Splice_Rec_2023534,Human_Splice_Rec_2023535,Human_Splice_Rec_2023552,Human_Splice_Rec_2023553,Human_Splice_Rec_2023564,Human_Splice_Rec_2023565 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_338592,RMVar_hsa_circ_329833,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_313541,RMVar_hsa_circ_195556,RMVar_hsa_circ_317076,RMVar_hsa_circ_299077,RMVar_hsa_circ_195560,RMVar_hsa_circ_195561,RMVar_hsa_circ_195559 69906 RMVar_ID_69906 Human_SNP_ID_667679458 m1A Human chr19 + 47155134 47155134 47155134 GTCACCCTCTAGGGAGAAAACTAAAGTTGCCAAAGTTAGCCAAGGAGTAGAAGATGGGCCCGACA GTCACCCTCTAGGGAGAAAACTAAAGTTGCCAGAGTTAGCCAAGGAGTAGAAGATGGGCCCGACA A G SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47155126..47155225 32194978 MeRIP-seq:(Medium) rs1428885530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54248,Human_RBP_ID_524394,Human_RBP_ID_13483395,Human_RBP_ID_23802628 Human_Splice_Rec_2023404,Human_Splice_Rec_2023405,Human_Splice_Rec_2023422,Human_Splice_Rec_2023430,Human_Splice_Rec_2023431,Human_Splice_Rec_2023444,Human_Splice_Rec_2023445,Human_Splice_Rec_2023454,Human_Splice_Rec_2023455,Human_Splice_Rec_2023482,Human_Splice_Rec_2023483,Human_Splice_Rec_2023504,Human_Splice_Rec_2023505,Human_Splice_Rec_2023522,Human_Splice_Rec_2023523,Human_Splice_Rec_2023538,Human_Splice_Rec_2023539,Human_Splice_Rec_2023556,Human_Splice_Rec_2023557,Human_Splice_Rec_2023570,Human_Splice_Rec_2023571 Human_miRNA_ID_2218816 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_299077,RMVar_hsa_circ_56834,RMVar_hsa_circ_195561,RMVar_hsa_circ_363271,RMVar_hsa_circ_356999 69907 RMVar_ID_69907 Human_SNP_ID_667679466 m1A Human chr19 + 47155164 47155164 47155164 CAAAGTTAGCCAAGGAGTAGAAGATGGGCCCGACACCAAGAGAGCAAAACTTGATTCTTCTGAGA CAAAGTTAGCCAAGGAGTAGAAGATGGGCCCGGCACCAAGAGAGCAAAACTTGATTCTTCTGAGA A G SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:47155101..47155225;chr19:47155101..47155200 26863196 MeRIP-seq:(Medium) rs11559276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524394,Human_RBP_ID_1568928,Human_RBP_ID_6775946,Human_RBP_ID_13483395,Human_RBP_ID_27469774 Human_Splice_Rec_2023404,Human_Splice_Rec_2023405,Human_Splice_Rec_2023422,Human_Splice_Rec_2023430,Human_Splice_Rec_2023431,Human_Splice_Rec_2023444,Human_Splice_Rec_2023445,Human_Splice_Rec_2023454,Human_Splice_Rec_2023455,Human_Splice_Rec_2023482,Human_Splice_Rec_2023483,Human_Splice_Rec_2023504,Human_Splice_Rec_2023505,Human_Splice_Rec_2023522,Human_Splice_Rec_2023523,Human_Splice_Rec_2023538,Human_Splice_Rec_2023539,Human_Splice_Rec_2023556,Human_Splice_Rec_2023557,Human_Splice_Rec_2023570,Human_Splice_Rec_2023571 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_299077,RMVar_hsa_circ_56834,RMVar_hsa_circ_195561,RMVar_hsa_circ_363271,RMVar_hsa_circ_356999 69908 RMVar_ID_69908 Human_SNP_ID_667679476 m1A Human chr19 + 47155199 47155199 47155199 CCAAGAGAGCAAAACTTGATTCTTCTGAGACAACGATGGTCAAAAAGGTATGTGTAACGTGGGGG CCAAGAGAGCAAAACTTGATTCTTCTGAGACAGCGATGGTCAAAAAGGTATGTGTAACGTGGGGG A G SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47155101..47155200 32194978 MeRIP-seq:(Medium) rs772912781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54249,Human_RBP_ID_911665,Human_RBP_ID_1568928,Human_RBP_ID_1890505 Human_Splice_Rec_2023404,Human_Splice_Rec_2023405,Human_Splice_Rec_2023422,Human_Splice_Rec_2023430,Human_Splice_Rec_2023431,Human_Splice_Rec_2023444,Human_Splice_Rec_2023445,Human_Splice_Rec_2023454,Human_Splice_Rec_2023455,Human_Splice_Rec_2023482,Human_Splice_Rec_2023483,Human_Splice_Rec_2023504,Human_Splice_Rec_2023505,Human_Splice_Rec_2023522,Human_Splice_Rec_2023523,Human_Splice_Rec_2023538,Human_Splice_Rec_2023539,Human_Splice_Rec_2023556,Human_Splice_Rec_2023557,Human_Splice_Rec_2023570,Human_Splice_Rec_2023571 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_299077,RMVar_hsa_circ_56834,RMVar_hsa_circ_195561,RMVar_hsa_circ_363271,RMVar_hsa_circ_356999 69909 RMVar_ID_69909 Human_SNP_ID_667697944 m1A Human chr19 + 47221527 47221527 47221527 GGTGGGCGGCAGAGGCGGGCGGCTCAGTCCCCACCCCCTCGGTCACCGCCACCTTCCGATGCTGA GGTGGGCGGCAGAGGCGGGCGGCTCAGTCCCCCCCCCCTCGGTCACCGCCACCTTCCGATGCTGA A C lnc-C5AR1-3 RNACentral:URS00008BE256 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47221479..47221655 26863196 MeRIP-seq:(Medium) rs1038132968 Functional Loss SNV dbSNP153 33..33 33 - - - 69910 RMVar_ID_69910 Human_SNP_ID_667699573 m1A Human chr19 - 47226654 47226654 47226654 CTGGCGGGCGGTCCCACCCAGGCGGCCCCGGGAGTCCGCGGGGAGGAGGAACAGTGGGCCCGGGA CTGGCGGGCGGTCCCACCCAGGCGGCCCCGGGTGTCCGCGGGGAGGAGGAACAGTGGGCCCGGGA T A BBC3 Ensembl:ENSG00000105327 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47226604..47226804 32194978 MeRIP-seq:(Medium) rs942210815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4539599,Human_RBP_ID_5088832,Human_RBP_ID_5320490,Human_RBP_ID_5651060,Human_RBP_ID_17670167,Human_RBP_ID_22446883,Human_RBP_ID_22977487 Human_Splice_Rec_2023583,Human_Splice_Rec_2023589,Human_Splice_Rec_2023595,Human_Splice_Rec_2023597 RMVar_hsa_circ_91604,RMVar_hsa_circ_127412,RMVar_hsa_circ_111052,RMVar_hsa_circ_195569,RMVar_hsa_circ_195570,RMVar_hsa_circ_195568 69911 RMVar_ID_69911 Human_SNP_ID_667700176 m1A Human chr19 + 47228358 47228358 47228358 ACACTGCCGAGGGCACCAGGCGGCCGAGCGGGAAGGGGCGCGGGCCGTCGCGGGCCAGGCCCTCT ACACTGCCGAGGGCACCAGGCGGCCGAGCGGGTAGGGGCGCGGGCCGTCGCGGGCCAGGCCCTCT A T lnc-C5AR1-3 RNACentral:URS00008BE256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47228318..47228491 26863196 MeRIP-seq:(Medium) rs1200328862 Functional Loss SNV dbSNP153 33..33 33 - - - 69912 RMVar_ID_69912 Human_SNP_ID_667704189 m1A Human chr19 - 47242982 47242981 47242983 CACCGCACATACACAATCACAATGACACACACAGCGACAGACACACAGGTCCCAGGAACACGCAG CACCGCACATACACAATCACAATGACACACA__GCGACAGACACACAGGTCCCAGGAACACGCAG CTG C lnc-BBC3-1,lnc-BBC3-2,lnc-BBC3-1:2 RNACentral:URS00008C123D,RNACentral:URS0000D56DEE,RNACentral:URS0000E4745B lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47242980..47243082 26863196 MeRIP-seq:(Medium) rs1267412345 Functional Loss DEL dbSNP153 32..33 33 - - - 69913 RMVar_ID_69913 Human_SNP_ID_667704460 m1A Human chr19 + 47243680 47243680 47243680 CCTAGTCTCTCTCCGCTACCTCTGTCTCTGCCATCTGTCTCTATCATCTCTGTCTCTCCCTGTCT CCTAGTCTCTCTCCGCTACCTCTGTCTCTGCCGTCTGTCTCTATCATCTCTGTCTCTCCCTGTCT A G lnc-C5AR1-3 RNACentral:URS00008BE256 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47243362..47244249 26863196 MeRIP-seq:(Medium) rs551624402 Functional Loss SNV dbSNP153 33..33 33 - - - 69914 RMVar_ID_69914 Human_SNP_ID_667704532 m1A Human chr19 - 47243888 47243888 47243888 GGGACAGCTGAGAGAGTCAGATGGAGCGACAGAGACAGAGATGGGGGAGACAGAGACACGGAGAG GGGACAGCTGAGAGAGTCAGATGGAGCGACAGGGACAGAGATGGGGGAGACAGAGACACGGAGAG T C lnc-BBC3-1,lnc-BBC3-1:2 RNACentral:URS00008C123D,RNACentral:URS0000E4745B lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47243838..47243982 26863196 MeRIP-seq:(Medium) rs1160671595 Functional Loss SNV dbSNP153 33..33 33 - - - 69915 RMVar_ID_69915 Human_SNP_ID_667709069 m1A Human chr19 - 47257525 47257525 47257525 AAAGCTCCAGCCTCAATCCGGCTGGGAATGCCAGGGCCACGTCCCCGACATCCTGGAAACCGCTC AAAGCTCCAGCCTCAATCCGGCTGGGAATGCCTGGGCCACGTCCCCGACATCCTGGAAACCGCTC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47257488..47257625 26863196 MeRIP-seq:(Medium) rs1222293969 Functional Loss SNV dbSNP153 33..33 33 - - - 69916 RMVar_ID_69916 Human_SNP_ID_667709070 m1A Human chr19 - 47257525 47257525 47257525 AAAGCTCCAGCCTCAATCCGGCTGGGAATGCCAGGGCCACGTCCCCGACATCCTGGAAACCGCTC AAAGCTCCAGCCTCAATCCGGCTGGGAATGCCGGGGCCACGTCCCCGACATCCTGGAAACCGCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47257488..47257625 26863196 MeRIP-seq:(Medium) rs1222293969 Functional Loss SNV dbSNP153 33..33 33 - - - 69917 RMVar_ID_69917 Human_SNP_ID_667709433 m1A Human chr19 + 47258583 47258583 47258583 GGTCTCAGGCAGCCACACTCGATTTGAAATCAAAGGAGGAGAAGGATGCTGAGTTGGACAAGAGG GGTCTCAGGCAGCCACACTCGATTTGAAATCAGAGGAGGAGAAGGATGCTGAGTTGGACAAGAGG A G CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47258558..47260364 32194978 MeRIP-seq:(Medium) rs902349516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585819 Human_Splice_Rec_2023604,Human_Splice_Rec_2023605,Human_Splice_Rec_2023630,Human_Splice_Rec_2023631,Human_Splice_Rec_2023652,Human_Splice_Rec_2023653,Human_Splice_Rec_2023660,Human_Splice_Rec_2023661,Human_Splice_Rec_2023664,Human_Splice_Rec_2023665 RMVar_hsa_circ_42359,RMVar_hsa_circ_117359,RMVar_hsa_circ_195571 69918 RMVar_ID_69918 Human_SNP_ID_667711509 m1A Human chr19 + 47264658 47264658 47264658 GAACATTGAGAAGATGAATGAGGAGATGGAGAAGATCGCCGAGTATGAGCGCAACCAGCGGGTCA GAACATTGAGAAGATGAATGAGGAGATGGAGAGGATCGCCGAGTATGAGCGCAACCAGCGGGTCA A G CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47258558..47264800 26863196 MeRIP-seq:(Medium) rs774015477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911674,Human_RBP_ID_3957238,Human_RBP_ID_13485335,Human_RBP_ID_18995194,Human_RBP_ID_26336486 Human_Splice_Rec_2023610,Human_Splice_Rec_2023611,Human_Splice_Rec_2023636,Human_Splice_Rec_2023637 RMVar_hsa_circ_76127,RMVar_hsa_circ_80689,RMVar_hsa_circ_195572,RMVar_hsa_circ_270794,RMVar_hsa_circ_355333,RMVar_hsa_circ_195573,RMVar_hsa_circ_195574 69919 RMVar_ID_69919 Human_SNP_ID_667711510 m1A Human chr19 + 47264658 47264658 47264658 GAACATTGAGAAGATGAATGAGGAGATGGAGAAGATCGCCGAGTATGAGCGCAACCAGCGGGTCA GAACATTGAGAAGATGAATGAGGAGATGGAGATGATCGCCGAGTATGAGCGCAACCAGCGGGTCA A T CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47258558..47264800 26863196 MeRIP-seq:(Medium) rs774015477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911674,Human_RBP_ID_3957238,Human_RBP_ID_13485335,Human_RBP_ID_18995194,Human_RBP_ID_26336486 Human_Splice_Rec_2023610,Human_Splice_Rec_2023611,Human_Splice_Rec_2023636,Human_Splice_Rec_2023637 RMVar_hsa_circ_76127,RMVar_hsa_circ_80689,RMVar_hsa_circ_195572,RMVar_hsa_circ_270794,RMVar_hsa_circ_355333,RMVar_hsa_circ_195573,RMVar_hsa_circ_195574 69920 RMVar_ID_69920 Human_SNP_ID_667712315 m1A Human chr19 + 47266708 47266708 47266708 GGAGTACCTGCGCTGGAAGCAGGAGAGGGAGAAGATCGACCAGGAGCGGCTGCAGAGGCACCGCA GGAGTACCTGCGCTGGAAGCAGGAGAGGGAGAGGATCGACCAGGAGCGGCTGCAGAGGCACCGCA A G CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47266659..47270432 26863196 MeRIP-seq:(Medium) rs1438570572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22977491 Human_Splice_Rec_2023614,Human_Splice_Rec_2023615,Human_Splice_Rec_2023640,Human_Splice_Rec_2023641,Human_Splice_Rec_2023667 RMVar_hsa_circ_76127,RMVar_hsa_circ_355333,RMVar_hsa_circ_195574 69921 RMVar_ID_69921 Human_SNP_ID_667713874 m1A Human chr19 + 47271383 47271383 47271383 ATGGGAGGACATAAGTGAGGATGAGGAAGAGGAGGAGATCGAGGTGGAAGAAGGTGATGAGGAGG ATGGGAGGACATAAGTGAGGATGAGGAAGAGGTGGAGATCGAGGTGGAAGAAGGTGATGAGGAGG A T CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:47266492..47271623;chr19:47266428..47271709 26863196 MeRIP-seq:(Medium) rs1389557939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145831,Human_RBP_ID_13485413,Human_RBP_ID_22449550,Human_RBP_ID_24545500,Human_RBP_ID_26336489,Human_RBP_ID_26472732,Human_RBP_ID_27815527 69922 RMVar_ID_69922 Human_SNP_ID_667715786 m1A Human chr19 + 47275213 47275213 47275213 CCCGCCGCTGCCTCCCTCTCCTGCCTCCTGGGAGTCCCCGGCGGGCCGCGACCCCAGCTCCAGCT CCCGCCGCTGCCTCCCTCTCCTGCCTCCTGGGTGTCCCCGGCGGGCCGCGACCCCAGCTCCAGCT A T INAFM1 Ensembl:ENSG00000257704 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47274101..47275413 26863196 MeRIP-seq:(Medium) rs1274079744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583891,Human_RBP_ID_5117765,Human_RBP_ID_5145345,Human_RBP_ID_8197879 RMVar_hsa_circ_115704,RMVar_hsa_circ_195575 69923 RMVar_ID_69923 Human_SNP_ID_667716193 m1A Human chr19 + 47276050 47276050 47276050 GGGTTCTGGGAATTGCTGTTGGTGTAATTATCATGTCAGGGACAGAGGCTGAATCACCCAGGGAT GGGTTCTGGGAATTGCTGTTGGTGTAATTATCCTGTCAGGGACAGAGGCTGAATCACCCAGGGAT A C lnc-C5AR1-3 RNACentral:URS00008BE256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47276002..47276106 26863196 MeRIP-seq:(Medium) rs1410912672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13485435 69924 RMVar_ID_69924 Human_SNP_ID_667737653 m1A Human chr19 + 47349407 47349407 47349407 GTGTACCGGGTTGTGGCGGCGATGGCTGTCGGAGTTGGGCCGCTTGGGGGTAGTTTGGGGTGCGA GTGTACCGGGTTGTGGCGGCGATGGCTGTCGGGGTTGGGCCGCTTGGGGGTAGTTTGGGGTGCGA A G DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:47349351..47350256;chr19:47349351..47349964 26863196 MeRIP-seq:(Medium) rs1301100587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5443300,Human_RBP_ID_9426302,Human_RBP_ID_18421588,Human_RBP_ID_26336492 RMVar_hsa_circ_106316,RMVar_hsa_circ_195576 69925 RMVar_ID_69925 Human_SNP_ID_667737655 m1A Human chr19 - 47349409 47349409 47349409 ACTCGCACCCCAAACTACCCCCAAGCGGCCCAACTCCGACAGCCATCGCCGCCACAACCCGGTAC ACTCGCACCCCAAACTACCCCCAAGCGGCCCACCTCCGACAGCCATCGCCGCCACAACCCGGTAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47349351..47350031 26863196 MeRIP-seq:(Medium) rs999156359 Functional Loss SNV dbSNP153 33..33 33 - - - 69926 RMVar_ID_69926 Human_SNP_ID_667737676 m1A Human chr19 - 47349460 47349460 47349460 TTCGGCTGCCTCCTACATTTCTCCTCATCTCGAGACTTCCCTCGCCCCTGGACTCGCACCCCAAA TTCGGCTGCCTCCTACATTTCTCCTCATCTCGCGACTTCCCTCGCCCCTGGACTCGCACCCCAAA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:47349371..47349507 26863196 MeRIP-seq:(Medium) rs1219433427 Functional Loss SNV dbSNP153 33..33 33 - - - 69927 RMVar_ID_69927 Human_SNP_ID_667745405 m1A Human chr19 + 47375566 47375566 47375566 GTTGCAGCAGCGCCGGGAGCGCCGGGCCCTGCACCAGCTGAAACGCCAGCACGAGGAGGGCGCGG GTTGCAGCAGCGCCGGGAGCGCCGGGCCCTGCTCCAGCTGAAACGCCAGCACGAGGAGGGCGCGG A T DHX34 Ensembl:ENSG00000134815 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47375517..47375629 26863196 MeRIP-seq:(Medium) rs1257775539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18995199 RMVar_hsa_circ_84184,RMVar_hsa_circ_106316,RMVar_hsa_circ_195576,RMVar_hsa_circ_50528,RMVar_hsa_circ_195581,RMVar_hsa_circ_116243,RMVar_hsa_circ_86430,RMVar_hsa_circ_195584,RMVar_hsa_circ_195585,RMVar_hsa_circ_195589,RMVar_hsa_circ_104747,RMVar_hsa_circ_9461,RMVar_hsa_circ_128104,RMVar_hsa_circ_195590 69928 RMVar_ID_69928 Human_SNP_ID_667747534 m1A Human chr19 + 47380979 47380979 47380979 GGGGGGCTACGCAGTCACTGACTTCCTCACCTACAACTGCCTCACGGTAAGCATGAACCCTCCTT GGGGGGCTACGCAGTCACTGACTTCCTCACCTGCAACTGCCTCACGGTAAGCATGAACCCTCCTT A G DHX34 Ensembl:ENSG00000134815 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47380929..47381026 26863196 MeRIP-seq:(Medium) rs199815627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524476,Human_RBP_ID_8836023,Human_RBP_ID_17270131,Human_RBP_ID_18736664,Human_RBP_ID_19093816,Human_RBP_ID_27469813 Human_Splice_Rec_2023717,Human_Splice_Rec_2023755 Human_miRNA_ID_2280648,Human_miRNA_ID_2460712,Human_miRNA_ID_2640916 RMVar_hsa_circ_84184,RMVar_hsa_circ_50528,RMVar_hsa_circ_195581,RMVar_hsa_circ_86430,RMVar_hsa_circ_195585,RMVar_hsa_circ_195589,RMVar_hsa_circ_104747 69929 RMVar_ID_69929 Human_SNP_ID_667755335 m1A Human chr19 - 47407359 47407359 47407359 CGCAGGACACGGGGCTCACCATCCTGCAAGTCAACAACTGGTGAGTGGCCCAGGAGGGCCCGCGG CGCAGGACACGGGGCTCACCATCCTGCAAGTCTACAACTGGTGAGTGGCCCAGGAGGGCCCGCGG T A MEIS3 Ensembl:ENSG00000105419 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47407351..47407451 32194978 MeRIP-seq:(Medium) rs764939746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2023774,Human_Splice_Rec_2023775,Human_Splice_Rec_2023798,Human_Splice_Rec_2023799,Human_Splice_Rec_2023823,Human_Splice_Rec_2023846,Human_Splice_Rec_2023847,Human_Splice_Rec_2023860,Human_Splice_Rec_2023861,Human_Splice_Rec_2023882,Human_Splice_Rec_2023883,Human_Splice_Rec_2023907,Human_Splice_Rec_2023920,Human_Splice_Rec_2023921,Human_Splice_Rec_2023943,Human_Splice_Rec_2023951 RMVar_hsa_circ_32857 69930 RMVar_ID_69930 Human_SNP_ID_667757710 m1A Human chr19 - 47415098 47415098 47415098 CTCCCCCCACCTCCCGCCCACGTTTTCAGATGATCCAGGCCATCCAGGTGCTGCGGTTCCACCTG CTCCCCCCACCTCCCGCCCACGTTTTCAGATGTTCCAGGCCATCCAGGTGCTGCGGTTCCACCTG T A MEIS3 Ensembl:ENSG00000105419 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47415062..47415986 32194978 MeRIP-seq:(Medium) rs1466147870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2023766,Human_Splice_Rec_2023767,Human_Splice_Rec_2023790,Human_Splice_Rec_2023791,Human_Splice_Rec_2023814,Human_Splice_Rec_2023815,Human_Splice_Rec_2023838,Human_Splice_Rec_2023839,Human_Splice_Rec_2023874,Human_Splice_Rec_2023875,Human_Splice_Rec_2023898,Human_Splice_Rec_2023899,Human_Splice_Rec_2023934,Human_Splice_Rec_2023935,Human_Splice_Rec_2023968,Human_Splice_Rec_2023976 RMVar_hsa_circ_32857 69931 RMVar_ID_69931 Human_SNP_ID_667758243 m1A Human chr19 - 47416832 47416832 47416832 TGGAGGTGACGTCTGCTCCTCTGATTCCTTCAACGAGGACATCGCTGCCTTTGCCAAGCAGGTGG TGGAGGTGACGTCTGCTCCTCTGATTCCTTCAGCGAGGACATCGCTGCCTTTGCCAAGCAGGTGG T C MEIS3 Ensembl:ENSG00000105419 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47416830..47417393 32194978 MeRIP-seq:(Medium) rs763306913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2023763,Human_Splice_Rec_2023787,Human_Splice_Rec_2023811,Human_Splice_Rec_2023835,Human_Splice_Rec_2023871,Human_Splice_Rec_2023895,Human_Splice_Rec_2023931,Human_Splice_Rec_2023965,Human_Splice_Rec_2023973 RMVar_hsa_circ_97736,RMVar_hsa_circ_195592,RMVar_hsa_circ_195594,RMVar_hsa_circ_288047,RMVar_hsa_circ_94627,RMVar_hsa_circ_195593,RMVar_hsa_circ_106176,RMVar_hsa_circ_195595,RMVar_hsa_circ_195596 69932 RMVar_ID_69932 Human_SNP_ID_667758461 m1A Human chr19 - 47417316 47417316 47417316 TGATGAGCTGCCGCACTACCCAGGCATCGTGGATGGCCCCGCAGCCCTGGCTAGCTTCCCAGAGA TGATGAGCTGCCGCACTACCCAGGCATCGTGGTTGGCCCCGCAGCCCTGGCTAGCTTCCCAGAGA T A MEIS3 Ensembl:ENSG00000105419 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:47417267..47417341;chr19:47417213..47417374 26863196 MeRIP-seq:(Medium) rs1387762426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524493 Human_Splice_Rec_2023760,Human_Splice_Rec_2023784,Human_Splice_Rec_2023808,Human_Splice_Rec_2023832,Human_Splice_Rec_2023892,Human_Splice_Rec_2023928,Human_Splice_Rec_2023962,Human_Splice_Rec_2023970 Human_miRNA_ID_3066418 RMVar_hsa_circ_97736,RMVar_hsa_circ_195592,RMVar_hsa_circ_195594,RMVar_hsa_circ_288047,RMVar_hsa_circ_94627,RMVar_hsa_circ_195593,RMVar_hsa_circ_106176,RMVar_hsa_circ_195595,RMVar_hsa_circ_195596 69933 RMVar_ID_69933 Human_SNP_ID_667759265 m1A Human chr19 + 47419422 47419422 47419422 CCCGGCTCTGGAGGGAATCGAACCGTCCCGAGACGGACACACCGGGGACCGCAGGGGGCGGGGGG CCCGGCTCTGGAGGGAATCGAACCGTCCCGAGGCGGACACACCGGGGACCGCAGGGGGCGGGGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:47419323..47419525 26863410 MeRIP-seq:(Medium) rs1302229510 Functional Loss SNV dbSNP153 33..33 33 - - - 69934 RMVar_ID_69934 Human_SNP_ID_667776408 m1A Human chr19 + 47480689 47480689 47480689 TCTGAGCTCCTCCCCGGTGACCAATTTCTCTAAGGTCTCACCGCCCGATTTCTCTGATGTCAGTG TCTGAGCTCCTCCCCGGTGACCAATTTCTCTAGGGTCTCACCGCCCGATTTCTCTGATGTCAGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47480684..47480784 32194978 MeRIP-seq:(Medium) rs1231319484 Functional Loss SNV dbSNP153 33..33 33 - - - 69935 RMVar_ID_69935 Human_SNP_ID_667777375 m1A Human chr19 - 47483984 47483984 47483984 AAGGTGCTCGGCTTCCGCTACCAAGACCTCCGACAGAAAATCCGGCCAGTGGCCAAGGAGCTGCA AAGGTGCTCGGCTTCCGCTACCAAGACCTCCGGCAGAAAATCCGGCCAGTGGCCAAGGAGCTGCA T C KPTN Ensembl:ENSG00000118162 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47483881..47484071 32194978 MeRIP-seq:(Medium) rs763064529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4539932 Human_Splice_Rec_2024049,Human_Splice_Rec_2024071,Human_Splice_Rec_2024095,Human_Splice_Rec_2024110,Human_Splice_Rec_2024111,Human_Splice_Rec_2024137,Human_Splice_Rec_2024149 Human_miRNA_ID_2156429,Human_miRNA_ID_2159989 RMVar_hsa_circ_195599,RMVar_hsa_circ_78759 69936 RMVar_ID_69936 Human_SNP_ID_667777414 m1A Human chr19 - 47484065 47484065 47484065 TTCTCGTCGCAGAGCAATGTGTACGGGCTGGCAGGCGGCGCCGGCGGGCGCGGGGAGCTGCTGGC TTCTCGTCGCAGAGCAATGTGTACGGGCTGGCGGGCGGCGCCGGCGGGCGCGGGGAGCTGCTGGC T C KPTN Ensembl:ENSG00000118162 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47484015..47484245 26863196 MeRIP-seq:(Medium) rs752995072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2024136,Human_Splice_Rec_2024148 Human_miRNA_ID_2398565 RMVar_hsa_circ_195599,RMVar_hsa_circ_78759 69937 RMVar_ID_69937 Human_SNP_ID_667777477 m1A Human chr19 - 47484170 47484170 47484170 GGTTGGGGCGGGGGCTGCGGAGAGGGTGCTTAACTGAGGGGCATGATGGGGGAGGCGGCCGTGGC GGTTGGGGCGGGGGCTGCGGAGAGGGTGCTTAGCTGAGGGGCATGATGGGGGAGGCGGCCGTGGC T C KPTN Ensembl:ENSG00000118162 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47483976..47484246 26863196 MeRIP-seq:(Medium) rs1180178130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826070,Human_RBP_ID_3586662,Human_RBP_ID_4558615,Human_RBP_ID_5145346,Human_RBP_ID_5377072,Human_RBP_ID_9425387,Human_RBP_ID_18420959,Human_RBP_ID_18945744,Human_RBP_ID_18995203,Human_RBP_ID_21980010,Human_RBP_ID_22592231,Human_RBP_ID_26336495 RMVar_hsa_circ_195599,RMVar_hsa_circ_78759 69938 RMVar_ID_69938 Human_SNP_ID_667778622 m1A Human chr19 - 47488391 47488391 47488391 AGCATGGCCAGCCTATCACCTGGTGTGCCCTCAGGTGAAGGAATACGACTCCATCTCCCGGCTGG AGCATGGCCAGCCTATCACCTGGTGTGCCCTCCGGTGAAGGAATACGACTCCATCTCCCGGCTGG T G NAPA,AC073548.1 Ensembl:ENSG00000105402,Ensembl:ENSG00000279861 Protein coding,Other intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47488351..47488400 32194978 MeRIP-seq:(Medium) rs113482197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907954,Human_RBP_ID_19090545,Human_RBP_ID_22448885,Human_RBP_ID_22662929 RMVar_hsa_circ_367677 69939 RMVar_ID_69939 Human_SNP_ID_667785426 m1A Human chr19 - 47512837 47512837 47512837 AGAGGGATCTTTACAAGAGAGGAAGGAACAGGAAAAGGGCTCTAGGCCACGCCCCTTGTTTGAGG AGAGGGATCTTTACAAGAGAGGAAGGAACAGGGAAAGGGCTCTAGGCCACGCCCCTTGTTTGAGG T C NAPA Ensembl:ENSG00000105402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47512831..47513351 26863196 MeRIP-seq:(Medium) rs1038784095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588486 69940 RMVar_ID_69940 Human_SNP_ID_667785500 m1A Human chr19 - 47513164 47513164 47513164 TAGGGTTGAGAGGAGCATGAGGCTCTGGGCAGAGGAAGGAGAAGGGAGTTTGGCAGGGGGCGGTG TAGGGTTGAGAGGAGCATGAGGCTCTGGGCAGGGGAAGGAGAAGGGAGTTTGGCAGGGGGCGGTG T C NAPA Ensembl:ENSG00000105402 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47513155..47513352 26863196 MeRIP-seq:(Medium) rs1473288192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6776835 69941 RMVar_ID_69941 Human_SNP_ID_667785501 m1A Human chr19 - 47513166 47513166 47513166 AGTAGGGTTGAGAGGAGCATGAGGCTCTGGGCAGAGGAAGGAGAAGGGAGTTTGGCAGGGGGCGG AGTAGGGTTGAGAGGAGCATGAGGCTCTGGGCGGAGGAAGGAGAAGGGAGTTTGGCAGGGGGCGG T C NAPA Ensembl:ENSG00000105402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47513164..47513371 26863196 MeRIP-seq:(Medium) rs1426537057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6776835 69942 RMVar_ID_69942 Human_SNP_ID_667785615 m1A Human chr19 - 47513651 47513651 47513651 CCTCGAGTAATAGGGATGACAGAGACATGCTGAGAAGAGGGATGGGAAAAGGCCTGGGAGACAGA CCTCGAGTAATAGGGATGACAGAGACATGCTGCGAAGAGGGATGGGAAAAGGCCTGGGAGACAGA T G NAPA Ensembl:ENSG00000105402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47513649..47513840 26863196 MeRIP-seq:(Medium) rs1222100584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2568148,Human_RBP_ID_3586666,Human_RBP_ID_6776838 69943 RMVar_ID_69943 Human_SNP_ID_667785874 m1A Human chr19 + 47514427 47514427 47514427 CCGCCTGAGAGCCTTCAAACAGACTCCCCTAGAGCTCCGAAAAGCCTCTGGACCTGGCTTCTCTC CCGCCTGAGAGCCTTCAAACAGACTCCCCTAGGGCTCCGAAAAGCCTCTGGACCTGGCTTCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47514421..47514834 26863196 MeRIP-seq:(Medium) rs184622615 Functional Loss SNV dbSNP153 33..33 33 - - - 69944 RMVar_ID_69944 Human_SNP_ID_667786009 m1A Human chr19 + 47514858 47514855 47514858 CTCAGCCCGGTTCTCACCCAAAGAGGCCAGAGAAGAAGGACTGCGAGTTCTTCACTTTGCGCTCC CTCAGCCCGGTTCTCACCCAAAGAGGCCAG___AGAAGGACTGCGAGTTCTTCACTTTGCGCTCC GAGA G lnc-BICRA-4 RNACentral:URS00008B6A7E lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47514851..47515000 32194978 MeRIP-seq:(Medium) rs760353871 Functional Loss DEL dbSNP153 31..33 33 - - - 69945 RMVar_ID_69945 Human_SNP_ID_667786045 m1A Human chr19 + 47514960 47514960 47514960 CGGAATTGTCCATGGCGGCCACAAAGGGACTCAGCAAAGCGCCTGACCCTGACCCTGGGAAGACT CGGAATTGTCCATGGCGGCCACAAAGGGACTCGGCAAAGCGCCTGACCCTGACCCTGGGAAGACT A G lnc-BICRA-4 RNACentral:URS00008B6A7E lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47514911..47515027 26863196 MeRIP-seq:(Medium) rs773021730 Functional Loss SNV dbSNP153 33..33 33 - - - 69946 RMVar_ID_69946 Human_SNP_ID_667810749 m1A Human chr19 - 47608439 47608439 47608439 GTCCAGGGGGAGCGCCGCAGGTCCGAAAAGATAGCGGGAGTCGAGGATGAAGGAAATGGAGGGGA GTCCAGGGGGAGCGCCGCAGGTCCGAAAAGATGGCGGGAGTCGAGGATGAAGGAAATGGAGGGGA T C AC010331.1 Ensembl:ENSG00000277383 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:47608245..47673584;chr19:47608200..47608640;chr19:47608233..47608620 26863196 MeRIP-seq:(Medium) rs1015036781 Functional Loss SNV dbSNP153 33..33 33 - - - 69947 RMVar_ID_69947 Human_SNP_ID_667811036 m1A Human chr19 + 47609166 47609166 47609166 GGAGACCCCGCGCCGACGGCTGCTCAAACATCAGGGTGAGTTTCTCACAATGTAGCAATTTCTCT GGAGACCCCGCGCCGACGGCTGCTCAAACATCGGGGTGAGTTTCTCACAATGTAGCAATTTCTCT A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47609157..47609344 26863196 MeRIP-seq:(Medium) rs1036623787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19093826 Human_Splice_Rec_2024529 69948 RMVar_ID_69948 Human_SNP_ID_667811037 m1A Human chr19 + 47609166 47609166 47609166 GGAGACCCCGCGCCGACGGCTGCTCAAACATCAGGGTGAGTTTCTCACAATGTAGCAATTTCTCT GGAGACCCCGCGCCGACGGCTGCTCAAACATCTGGGTGAGTTTCTCACAATGTAGCAATTTCTCT A T AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47609157..47609344 26863196 MeRIP-seq:(Medium) rs1036623787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19093826 Human_Splice_Rec_2024529 69949 RMVar_ID_69949 Human_SNP_ID_667824926 m1A Human chr19 - 47658952 47658952 47658952 AAGTACAGGCATTCGGGGTGGGTGGCGGAAATACAAAAGAAATGATTATGTTCACCGGACACAGG AAGTACAGGCATTCGGGGTGGGTGGCGGAAATGCAAAAGAAATGATTATGTTCACCGGACACAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47658827..47659028 26863196 MeRIP-seq:(Medium) rs974077653 Functional Loss SNV dbSNP153 33..33 33 - - - 69950 RMVar_ID_69950 Human_SNP_ID_667828349 m1A Human chr19 + 47671565 47671565 47671565 GTGCAGGAAGTAATGAAGGGATGAGTGGCTGGAAGGATGGGTCTGTGTGGGTATTTGGCAGAAGG GTGCAGGAAGTAATGAAGGGATGAGTGGCTGGGAGGATGGGTCTGTGTGGGTATTTGGCAGAAGG A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47671473..47671927 26863196 MeRIP-seq:(Medium) rs1400218509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587258 RMVar_hsa_circ_21571,RMVar_hsa_circ_73163 69951 RMVar_ID_69951 Human_SNP_ID_667828422 m1A Human chr19 + 47671774 47671774 47671774 AGGTAGATGGATGGAAGGATGGAGGGATGGGCAAGTAGATGGAAGGATGGAGGGATGGGTAGCTA AGGTAGATGGATGGAAGGATGGAGGGATGGGCGAGTAGATGGAAGGATGGAGGGATGGGTAGCTA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47671350..47671941 26863196 MeRIP-seq:(Medium) rs1311975578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191682 RMVar_hsa_circ_21571,RMVar_hsa_circ_73163 69952 RMVar_ID_69952 Human_SNP_ID_667828423 m1A Human chr19 + 47671775 47671775 47671775 GGTAGATGGATGGAAGGATGGAGGGATGGGCAAGTAGATGGAAGGATGGAGGGATGGGTAGCTAG GGTAGATGGATGGAAGGATGGAGGGATGGGCAGGTAGATGGAAGGATGGAGGGATGGGTAGCTAG A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47671437..47671948 26863196 MeRIP-seq:(Medium) rs1217726301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191682 RMVar_hsa_circ_21571,RMVar_hsa_circ_73163 69953 RMVar_ID_69953 Human_SNP_ID_667828535 m1A Human chr19 - 47672090 47672071 47672091 CATCCTCCATCCTTCCATCCATCTACCTACCGATCCCTCCATCCATCCACCCATCCCTCCATCCT CATCCTCCATCCTTCCATCCATCTACCTACC____________________CATCCCTCCATCCT GGGTGGATGGATGGAGGGATC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47672001..47672334 26863196 MeRIP-seq:(Medium) rs1342848823 Functional Loss DEL dbSNP153 32..51 33 - - - 69954 RMVar_ID_69954 Human_SNP_ID_667828565 m1A Human chr19 - 47672125 47672125 47672125 TACCCATGCTCCATCCTTCCATCCATCTACCTACCCATCCTCCATCCTTCCATCCATCTACCTAC TACCCATGCTCCATCCTTCCATCCATCTACCTCCCCATCCTCCATCCTTCCATCCATCTACCTAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47672085..47672214 26863196 MeRIP-seq:(Medium) rs577927647 Functional Loss SNV dbSNP153 33..33 33 - - - 69955 RMVar_ID_69955 Human_SNP_ID_667828761 m1A Human chr19 + 47672950 47672950 47672950 CCCCTCTCCCTTGCTTCTGCCTCAGTTTCCCCACCACCCTCCCCTTCCTTGGGAACACATTGCAG CCCCTCTCCCTTGCTTCTGCCTCAGTTTCCCCGCCACCCTCCCCTTCCTTGGGAACACATTGCAG A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47672944..47673048 26863196 MeRIP-seq:(Medium) rs1274114502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583901 RMVar_hsa_circ_21571,RMVar_hsa_circ_73163 69956 RMVar_ID_69956 Human_SNP_ID_667829130 m1A Human chr19 + 47674235 47674235 47674235 AAAGGTGGGAGAGAGCTTGGCATGGTTGAGGAACAGGAAGGAGGCTGATGGGGCCAAACTGAAGG AAAGGTGGGAGAGAGCTTGGCATGGTTGAGGAGCAGGAAGGAGGCTGATGGGGCCAAACTGAAGG A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47674071..47674404 26863196 MeRIP-seq:(Medium) rs923263726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22974833 RMVar_hsa_circ_73163 69957 RMVar_ID_69957 Human_SNP_ID_667831292 m1A Human chr19 - 47681080 47681080 47681080 GGGGCTGCTGCGCCTGCGGCTGCTGGAGGCCCAGGGGCAGGGGTGTGCTGACCGCGGGGGGCGCC GGGGCTGCTGCGCCTGCGGCTGCTGGAGGCCCGGGGGCAGGGGTGTGCTGACCGCGGGGGGCGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47680824..47681161 26863196 MeRIP-seq:(Medium) rs1249578820 Functional Loss SNV dbSNP153 33..33 33 - - - 69958 RMVar_ID_69958 Human_SNP_ID_667831523 m1A Human chr19 + 47681551 47681550 47681552 AGGCAGTGAGAGGGACTGGCAGACAGACAGACAAAGAGAGGGACCAGTGAACAGACAGAAGGGTA AGGCAGTGAGAGGGACTGGCAGACAGACAGAC__AGAGAGGGACCAGTGAACAGACAGAAGGGTA CAA C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47681404..47681759 26863196 MeRIP-seq:(Medium) rs748046827 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5145348,Human_RBP_ID_5588113,Human_RBP_ID_13488217 RMVar_hsa_circ_60635 69959 RMVar_ID_69959 Human_SNP_ID_667831525 m1A Human chr19 + 47681551 47681551 47681551 AGGCAGTGAGAGGGACTGGCAGACAGACAGACAAAGAGAGGGACCAGTGAACAGACAGAAGGGTA AGGCAGTGAGAGGGACTGGCAGACAGACAGACTAAGAGAGGGACCAGTGAACAGACAGAAGGGTA A T AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47681404..47681759 26863196 MeRIP-seq:(Medium) rs1028686784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145348,Human_RBP_ID_5588113,Human_RBP_ID_13488217 RMVar_hsa_circ_60635 69960 RMVar_ID_69960 Human_SNP_ID_667835251 m1A Human chr19 - 47694369 47694369 47694369 GGGCCTGGGGCAGTAGGGGCCGGGTTGCTGGCAGGCGGGGGAACGCCTAGCTGGTTTTGGATGAC GGGCCTGGGGCAGTAGGGGCCGGGTTGCTGGCGGGCGGGGGAACGCCTAGCTGGTTTTGGATGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47694321..47694599 26863196 MeRIP-seq:(Medium) rs1199584354 Functional Loss SNV dbSNP153 33..33 33 - - - 69961 RMVar_ID_69961 Human_SNP_ID_667836819 m1A Human chr19 - 47698761 47698761 47698761 GGAGGCCTCACCTTTGTGGTAGTCACTGGGGGAGGGGAGGGCGCCCTGGTAGACATGGTAGGGCA GGAGGCCTCACCTTTGTGGTAGTCACTGGGGGTGGGGAGGGCGCCCTGGTAGACATGGTAGGGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47698713..47698995 26863196 MeRIP-seq:(Medium) rs563867740 Functional Loss SNV dbSNP153 33..33 33 - - - 69962 RMVar_ID_69962 Human_SNP_ID_667837877 m1A Human chr19 + 47701773 47701773 47701773 CCCGCTACCCTCAAGGTGGCCGAGCCCCCGCCACGGCCGCCACCACCACCGCCGCCCACGGGCCA CCCGCTACCCTCAAGGTGGCCGAGCCCCCGCCGCGGCCGCCACCACCACCGCCGCCCACGGGCCA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47701730..47701896 26863196 MeRIP-seq:(Medium) rs769275530 Functional Loss SNV dbSNP153 33..33 33 - - - 69963 RMVar_ID_69963 Human_SNP_ID_667837894 m1A Human chr19 + 47701788 47701788 47701788 GTGGCCGAGCCCCCGCCACGGCCGCCACCACCACCGCCGCCCACGGGCCAGATGAACGGCACGGT GTGGCCGAGCCCCCGCCACGGCCGCCACCACCGCCGCCGCCCACGGGCCAGATGAACGGCACGGT A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47701745..47701993 26863196 MeRIP-seq:(Medium) rs1568581830 Functional Loss SNV dbSNP153 33..33 33 - - - 69964 RMVar_ID_69964 Human_SNP_ID_667837914 m1A Human chr19 + 47701826 47701826 47701826 GCCCACGGGCCAGATGAACGGCACGGTGGACCACCCGCCGCCTGCCGCCCCCGAGCGCAAGCCCC GCCCACGGGCCAGATGAACGGCACGGTGGACCCCCCGCCGCCTGCCGCCCCCGAGCGCAAGCCCC A C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47701783..47701935 26863196 MeRIP-seq:(Medium) rs960674073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5293443 69965 RMVar_ID_69965 Human_SNP_ID_667838160 m1A Human chr19 + 47702270 47702270 47702270 GAGCGCCATCGACAGCATCCTGAACCTGCAGCAGGCCCCCGGCCGGACGCCCGCGCCCTCGTACC GAGCGCCATCGACAGCATCCTGAACCTGCAGCCGGCCCCCGGCCGGACGCCCGCGCCCTCGTACC A C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:47702225..47702438;chr19:47702221..47702429 26863196 MeRIP-seq:(Medium) rs756377499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587641 69966 RMVar_ID_69966 Human_SNP_ID_667843167 m1A Human chr19 - 47718867 47718831 47718867 CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAGACCCCAGTCCCTCCTCCCTCAGACCCAGGAGTC CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAG_________________________________ CCTGGACTCCTGGGTCTGAGGGAGGAGGGACTGGGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47718863..47719004 26863196 MeRIP-seq:(Medium) rs1568588067 Functional Loss DEL dbSNP153 33..65 33 - - - 69967 RMVar_ID_69967 Human_SNP_ID_667843186 m1A Human chr19 - 47718867 47718867 47718867 CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAGACCCCAGTCCCTCCTCCCTCAGACCCAGGAGTC CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAGGCCCCAGTCCCTCCTCCCTCAGACCCAGGAGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47718863..47719004 26863196 MeRIP-seq:(Medium) rs28480246 Functional Loss SNV dbSNP153 33..33 33 - - - 69968 RMVar_ID_69968 Human_SNP_ID_667843187 m1A Human chr19 - 47718867 47718867 47718867 CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAGACCCCAGTCCCTCCTCCCTCAGACCCAGGAGTC CAGCTCCTCCTCCCTCAGACCCAGGAGTCCAGCCCCCAGTCCCTCCTCCCTCAGACCCAGGAGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47718863..47719004 26863196 MeRIP-seq:(Medium) rs28480246 Functional Loss SNV dbSNP153 33..33 33 - - - 69969 RMVar_ID_69969 Human_SNP_ID_667846246 m1A Human chr19 - 47729424 47729424 47729424 TCCAGGCTCCTAGACTCTCCTGCCTTGAATCCACCCTCCAAAAGGTAGCTTGAGTCTAATTATCT TCCAGGCTCCTAGACTCTCCTGCCTTGAATCCCCCCTCCAAAAGGTAGCTTGAGTCTAATTATCT T G HSALNG0126789 RNACentral:URS0000EBCD76 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47729422..47729719 26863196 MeRIP-seq:(Medium) rs1270289277 Functional Loss SNV dbSNP153 33..33 33 - - - 69970 RMVar_ID_69970 Human_SNP_ID_667846291 m1A Human chr19 - 47729586 47729586 47729586 TCCCTGCCTGCCCAGCTTCCTGCCCCGCCTCCACCCTGGCAGCCTCCCCCTGAGAAAGTTCCATC TCCCTGCCTGCCCAGCTTCCTGCCCCGCCTCCGCCCTGGCAGCCTCCCCCTGAGAAAGTTCCATC T C HSALNG0126789 RNACentral:URS0000EBCD76 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47729561..47729690 26863196 MeRIP-seq:(Medium) rs1416377930 Functional Loss SNV dbSNP153 33..33 33 - - - 69971 RMVar_ID_69971 Human_SNP_ID_667846360 m1A Human chr19 - 47729836 47729836 47729836 GACTGAGAGAGAGGTAGAAAGGAGACTGACATAGAGACAGAAAAAGAGAGAGAGAGACACTGCAG GACTGAGAGAGAGGTAGAAAGGAGACTGACATGGAGACAGAAAAAGAGAGAGAGAGACACTGCAG T C HSALNG0126789 RNACentral:URS0000EBCD76 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47729834..47730007 26863196 MeRIP-seq:(Medium) rs866839418 Functional Loss SNV dbSNP153 33..33 33 - - - 69972 RMVar_ID_69972 Human_SNP_ID_667846411 m1A Human chr19 + 47730061 47730061 47730061 GGTCCCTTGGCGGGAGCTGGAGCACAAGGCCCAGGGACAGAGGGGTGGGTCCGGGCCAGACACCT GGTCCCTTGGCGGGAGCTGGAGCACAAGGCCCGGGGACAGAGGGGTGGGTCCGGGCCAGACACCT A G EHD2,AC010519.1 Ensembl:ENSG00000024422,Ensembl:ENSG00000268746 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47730060..47730183 26863196 MeRIP-seq:(Medium) rs1223840304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80012,RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_271893,RMVar_hsa_circ_195614,RMVar_hsa_circ_195613,RMVar_hsa_circ_335457,RMVar_hsa_circ_195616 69973 RMVar_ID_69973 Human_SNP_ID_667846412 m1A Human chr19 + 47730061 47730061 47730061 GGTCCCTTGGCGGGAGCTGGAGCACAAGGCCCAGGGACAGAGGGGTGGGTCCGGGCCAGACACCT GGTCCCTTGGCGGGAGCTGGAGCACAAGGCCCTGGGACAGAGGGGTGGGTCCGGGCCAGACACCT A T EHD2,AC010519.1 Ensembl:ENSG00000024422,Ensembl:ENSG00000268746 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47730060..47730183 26863196 MeRIP-seq:(Medium) rs1223840304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80012,RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_271893,RMVar_hsa_circ_195614,RMVar_hsa_circ_195613,RMVar_hsa_circ_335457,RMVar_hsa_circ_195616 69974 RMVar_ID_69974 Human_SNP_ID_667849604 m1A Human chr19 + 47740999 47740999 47740999 CATCGCCAAGCTCATGCCCCTGCTGCGGCAGGAGGAGCTGGAGAGCACCGAGGTGGGCGTGCAGG CATCGCCAAGCTCATGCCCCTGCTGCGGCAGGGGGAGCTGGAGAGCACCGAGGTGGGCGTGCAGG A G EHD2 Ensembl:ENSG00000024422 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47740949..47741450 32194978 MeRIP-seq:(Medium) rs1483264468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137130 RMVar_hsa_circ_80012,RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_195614,RMVar_hsa_circ_100424,RMVar_hsa_circ_195616,RMVar_hsa_circ_195618,RMVar_hsa_circ_195619,RMVar_hsa_circ_116346 69975 RMVar_ID_69975 Human_SNP_ID_667849650 m1A Human chr19 + 47741104 47741102 47741105 GCGGGGACCTGACGAGGCCATGGAGGACGGCGAGGAGGGCTCGGACGACGAGGCCGAGTGGGTGG GCGGGGACCTGACGAGGCCATGGAGGACGGC___GAGGGCTCGGACGACGAGGCCGAGTGGGTGG CGAG C EHD2 Ensembl:ENSG00000024422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47740945..47741200 26863196 MeRIP-seq:(Medium) rs553879219 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5321799,Human_RBP_ID_27469925 Human_miRNA_ID_2937760 RMVar_hsa_circ_80012,RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_195614,RMVar_hsa_circ_100424,RMVar_hsa_circ_195616,RMVar_hsa_circ_195618,RMVar_hsa_circ_195619,RMVar_hsa_circ_116346 69976 RMVar_ID_69976 Human_SNP_ID_667849670 m1A Human chr19 + 47741146 47741146 47741146 GGACGACGAGGCCGAGTGGGTGGTGACCAAGGACAAGTCCAAATACGACGAGATCTTCTACAACC GGACGACGAGGCCGAGTGGGTGGTGACCAAGGGCAAGTCCAAATACGACGAGATCTTCTACAACC A G EHD2 Ensembl:ENSG00000024422 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:47741101..47741175 26863196 MeRIP-seq:(Medium) rs764781083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2255699 RMVar_hsa_circ_80012,RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_195614,RMVar_hsa_circ_100424,RMVar_hsa_circ_195616,RMVar_hsa_circ_195618,RMVar_hsa_circ_195619,RMVar_hsa_circ_116346 69977 RMVar_ID_69977 Human_SNP_ID_667850023 m1A Human chr19 - 47742068 47742067 47742068 GGGCTTTCCCCGAGCAAGGGAAGGGGCTGCGGAGGGGCCCATCTGAGGAAGCAGTAGGTGTGTCT GGGCTTTCCCCGAGCAAGGGAAGGGGCTGCGG_GGGGCCCATCTGAGGAAGCAGTAGGTGTGTCT CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47742021..47742124 32194978 MeRIP-seq:(Medium) rs536437976 Functional Loss DEL dbSNP153 33..33 33 - - - 69978 RMVar_ID_69978 Human_SNP_ID_667850083 m1A Human chr19 - 47742225 47742220 47742225 GGGTGTGGACAGAACTGGGGGCAAAAACAAAAAAGAAGGAAGGAAGGAAAGAAAGAAATGGGTAT GGGTGTGGACAGAACTGGGGGCAAAAACAAAA_____GGAAGGAAGGAAAGAAAGAAATGGGTAT CTTCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47742201..47742225 26863196 MeRIP-seq:(Medium) rs1401142967 Functional Loss DEL dbSNP153 33..37 33 - - - 69979 RMVar_ID_69979 Human_SNP_ID_667850084 m1A Human chr19 - 47742225 47742223 47742226 GGGTGTGGACAGAACTGGGGGCAAAAACAAAAAAGAAGGAAGGAAGGAAAGAAAGAAATGGGTAT GGGTGTGGACAGAACTGGGGGCAAAAACAAA___GAAGGAAGGAAGGAAAGAAAGAAATGGGTAT CTTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47742201..47742225 26863196 MeRIP-seq:(Medium) rs1221960817 Functional Loss DEL dbSNP153 32..34 33 - - - 69980 RMVar_ID_69980 Human_SNP_ID_667850200 m1A Human chr19 - 47742628 47742628 47742628 ATATCTCCAAGGGGGCACAGTATCAGAGGAGCAGGATGGAAGGGGCTTTTCTGCCTGCTACGGGA ATATCTCCAAGGGGGCACAGTATCAGAGGAGCCGGATGGAAGGGGCTTTTCTGCCTGCTACGGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47742579..47742825 26863196 MeRIP-seq:(Medium) rs1397513679 Functional Loss SNV dbSNP153 33..33 33 - - - 69981 RMVar_ID_69981 Human_SNP_ID_667850211 m1A Human chr19 - 47742683 47742683 47742683 GGGCCAGGAGCAGGCTGGGCAGTTCCAGCCACAGACACGTGGGTGGAGGACGGAAATATCTCCAA GGGCCAGGAGCAGGCTGGGCAGTTCCAGCCACGGACACGTGGGTGGAGGACGGAAATATCTCCAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47742576..47742855 26863196 MeRIP-seq:(Medium) rs1261027331 Functional Loss SNV dbSNP153 33..33 33 - - - 69982 RMVar_ID_69982 Human_SNP_ID_667851289 m1A Human chr19 + 47745776 47745776 47745776 AGTTCCTGGAAGACGTGCGGCTACAGGAGCGCACGAGCGGGTACGTTGGGCGGGACTTCCGGGAG AGTTCCTGGAAGACGTGCGGCTACAGGAGCGCGCGAGCGGGTACGTTGGGCGGGACTTCCGGGAG A G NOP53 Ensembl:ENSG00000105373 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47745576..47745928 32194978 MeRIP-seq:(Medium) rs1343723525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911688,Human_RBP_ID_9381221,Human_RBP_ID_17935031,Human_RBP_ID_18998293 Human_Splice_Rec_2024587,Human_Splice_Rec_2024611,Human_Splice_Rec_2024621,Human_Splice_Rec_2024641,Human_Splice_Rec_2024659 69983 RMVar_ID_69983 Human_SNP_ID_667851802 m1A Human chr19 - 47746977 47746975 47746978 CACGAAGAAGAGTTTTTCATTTGGGGCCTCTGACAACAAGCCACTGGGGGACAGAAATGCAGAAC CACGAAGAAGAGTTTTTCATTTGGGGCCTCT___AACAAGCCACTGGGGGACAGAAATGCAGAAC TGTC T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47746951..47751153 32194978 MeRIP-seq:(Medium) rs775704008 Functional Loss DEL dbSNP153 32..34 33 - - - 69984 RMVar_ID_69984 Human_SNP_ID_667852874 m1A Human chr19 - 47750288 47750286 47750288 GGAAAGAAGGGCCCAGGGATGCTGGGACACTCACTCTTTGGGGGCAGGGACTTTGGATGTGTTCT GGAAAGAAGGGCCCAGGGATGCTGGGACACTC__TCTTTGGGGGCAGGGACTTTGGATGTGTTCT AGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47750127..47750335 26863196 MeRIP-seq:(Medium) rs767753747 Functional Loss DEL dbSNP153 33..34 33 - - - 69985 RMVar_ID_69985 Human_SNP_ID_667853357 m1A Human chr19 + 47751589 47751589 47751589 TTTCCTGGAGCAGACCAAGAAGAAAGGAGTGAAGGTGAGATGTGTGGGAAGGGCATCCTGGGTGA TTTCCTGGAGCAGACCAAGAAGAAAGGAGTGAGGGTGAGATGTGTGGGAAGGGCATCCTGGGTGA A G NOP53 Ensembl:ENSG00000105373 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47751551..47751600 26863196 MeRIP-seq:(Medium) rs200973335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957249,Human_RBP_ID_5145349 Human_Splice_Rec_2024594,Human_Splice_Rec_2024595,Human_Splice_Rec_2024618,Human_Splice_Rec_2024619,Human_Splice_Rec_2024628,Human_Splice_Rec_2024629,Human_Splice_Rec_2024648,Human_Splice_Rec_2024649,Human_Splice_Rec_2024668,Human_Splice_Rec_2024669,Human_Splice_Rec_2024674,Human_Splice_Rec_2024675,Human_Splice_Rec_2024694,Human_Splice_Rec_2024695,Human_Splice_Rec_2024706,Human_Splice_Rec_2024707 RMVar_hsa_circ_41914,RMVar_hsa_circ_268409,RMVar_hsa_circ_29185 69986 RMVar_ID_69986 Human_SNP_ID_667853708 m1A Human chr19 - 47752590 47752590 47752590 GACGGGGCAGTGTACCTGGTGGTCTTCAAAGGATGGATTGTAGGAAGCTCCGGCAGGCGCCACCT GACGGGGCAGTGTACCTGGTGGTCTTCAAAGGGTGGATTGTAGGAAGCTCCGGCAGGCGCCACCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47752469..47752629 26863196 MeRIP-seq:(Medium) rs776596607 Functional Loss SNV dbSNP153 33..33 33 - - - 69987 RMVar_ID_69987 Human_SNP_ID_667854469 m1A Human chr19 - 47754809 47754809 47754809 CTGTGGTGGCCAGGCGGGCGGGCGTGGGACAGACCTCGGCATCCCCAGCCTCCGGCCCCTCGCCC CTGTGGTGGCCAGGCGGGCGGGCGTGGGACAGCCCTCGGCATCCCCAGCCTCCGGCCCCTCGCCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:47754635..47754940 26863196 MeRIP-seq:(Medium) rs1305022354 Functional Loss SNV dbSNP153 33..33 33 - - - 69988 RMVar_ID_69988 Human_SNP_ID_667854793 m1A Human chr19 + 47755417 47755417 47755417 GGCACCAGGAGCTGTTCCGGCTGCGCGGGATCAAGGCCCAGGTGGCCCTGAGGCTGGCGGAGCTG GGCACCAGGAGCTGTTCCGGCTGCGCGGGATCGAGGCCCAGGTGGCCCTGAGGCTGGCGGAGCTG A G NOP53 Ensembl:ENSG00000105373 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:47755401..47755425 26863196 MeRIP-seq:(Medium) rs1172403709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17928786,Human_RBP_ID_18995214 Human_Splice_Rec_2024602,Human_Splice_Rec_2024636,Human_Splice_Rec_2024652 RMVar_hsa_circ_268409 69989 RMVar_ID_69989 Human_SNP_ID_667855331 m1A Human chr19 + 47756599 47756599 47756599 CAGAGGAGGAATATGATCGAGCCTCGAGAGAGAGCCAAGTAAGGGGCGGCCGGGGCTGCTGTGGG CAGAGGAGGAATATGATCGAGCCTCGAGAGAGCGCCAAGTAAGGGGCGGCCGGGGCTGCTGTGGG A C NOP53 Ensembl:ENSG00000105373 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47756483..47756699 26863196 MeRIP-seq:(Medium) rs770241150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17935035,Human_RBP_ID_18470631,Human_RBP_ID_18998304,Human_RBP_ID_26816084 Human_Splice_Rec_2024606,Human_Splice_Rec_2024607,Human_Splice_Rec_2024638,Human_Splice_Rec_2024639,Human_Splice_Rec_2024655,Human_Splice_Rec_2024684,Human_Splice_Rec_2024685,Human_Splice_Rec_2024700,Human_Splice_Rec_2024701,Human_Splice_Rec_2024714,Human_Splice_Rec_2024715,Human_Splice_Rec_2024722,Human_Splice_Rec_2024723 RMVar_hsa_circ_268409 69990 RMVar_ID_69990 Human_SNP_ID_667855377 m1A Human chr19 - 47756680 47756680 47756680 CTTCACCTTGTACTTGCGTTTGAACCTGGAGCAGGGACAATGGAGCAATCAGTGCCCGGGGCCAA CTTCACCTTGTACTTGCGTTTGAACCTGGAGCGGGGACAATGGAGCAATCAGTGCCCGGGGCCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47756676..47756725 26863196 MeRIP-seq:(Medium) rs761828269 Functional Loss SNV dbSNP153 33..33 33 - - - 69991 RMVar_ID_69991 Human_SNP_ID_667858263 m1A Human chr19 - 47765812 47765812 47765812 CAGCCTTGTGTGGGCAGGCTGGGGAGTAGCTCATCCGCAGCCCCGATTCTCTCCCACACCCTCCC CAGCCTTGTGTGGGCAGGCTGGGGAGTAGCTCTTCCGCAGCCCCGATTCTCTCCCACACCCTCCC T A NOP53-AS1 Ensembl:ENSG00000269656 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47765763..47765893 26863196 MeRIP-seq:(Medium) rs941261015 Functional Loss SNV dbSNP153 33..33 33 - - - 69992 RMVar_ID_69992 Human_SNP_ID_667858447 m1A Human chr19 - 47766473 47766473 47766473 TGTCCGCCTCCAGGCCCACTGCCAGAATCCACACCCTTCCCTCCTGCTCACCCTCTACCTTAAAC TGTCCGCCTCCAGGCCCACTGCCAGAATCCACCCCCTTCCCTCCTGCTCACCCTCTACCTTAAAC T G NOP53-AS1 Ensembl:ENSG00000269656 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47766371..47766516 26863196 MeRIP-seq:(Medium) rs1305941824 Functional Loss SNV dbSNP153 33..33 33 - - - 69993 RMVar_ID_69993 Human_SNP_ID_667861989 m1A Human chr19 - 47778753 47778753 47778753 GGCTCGGGGCTGCCACATCCGCTGAGGAGCGGACGCCCGGGCCACACTAACCTCCCACCTGGACG GGCTCGGGGCTGCCACATCCGCTGAGGAGCGGCCGCCCGGGCCACACTAACCTCCCACCTGGACG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47778701..47779346 26863196 MeRIP-seq:(Medium) rs1182340869 Functional Loss SNV dbSNP153 33..33 33 - - - 69994 RMVar_ID_69994 Human_SNP_ID_667862031 m1A Human chr19 + 47778811 47778811 47778811 CCGAGCCATGGCTCTCGCCGTCCGAGTCGTTTATTGGTAAGCCCAGCGGCCAGCGGCCCCCGTCC CCGAGCCATGGCTCTCGCCGTCCGAGTCGTTTGTTGGTAAGCCCAGCGGCCAGCGGCCCCCGTCC A G SELENOW Ensembl:ENSG00000178980 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47778761..47779256 26863196 MeRIP-seq:(Medium) rs753349512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911693,Human_RBP_ID_4558621,Human_RBP_ID_5117031,Human_RBP_ID_5370554,Human_RBP_ID_9330177,Human_RBP_ID_19090561,Human_RBP_ID_22476689,Human_RBP_ID_26785893 Human_Splice_Rec_2024733,Human_Splice_Rec_2024743,Human_Splice_Rec_2024753,Human_Splice_Rec_2024763,Human_Splice_Rec_2024773,Human_Splice_Rec_2024781,Human_Splice_Rec_2024789,Human_Splice_Rec_2024799,Human_Splice_Rec_2024801 RMVar_hsa_circ_92650,RMVar_hsa_circ_195623 69995 RMVar_ID_69995 Human_SNP_ID_667862360 m1A Human chr19 + 47779729 47779719 47779729 TGCTTGGGAGGCTGAGGCAGGAGGATCACTGGAGCCCGGAAGGCGGAAGTTGCAGTGAGCTGAAA TGCTTGGGAGGCTGAGGCAGGAG__________GCCCGGAAGGCGGAAGTTGCAGTGAGCTGAAA GGATCACTGGA G SELENOW Ensembl:ENSG00000178980 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47779724..47780734 26863196 MeRIP-seq:(Medium) rs1288510872 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_772156 Human_Splice_Rec_2024802 RMVar_hsa_circ_92650,RMVar_hsa_circ_195623 69996 RMVar_ID_69996 Human_SNP_ID_667862455 m1A Human chr19 - 47780088 47780088 47780088 GCTCCTAGATTCTGAACACCTTCCCAGTCCCCAGGGTGAAATACAGGCTCACCCAACCCCCACAG GCTCCTAGATTCTGAACACCTTCCCAGTCCCCGGGGTGAAATACAGGCTCACCCAACCCCCACAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47780081..47780488 26863196 MeRIP-seq:(Medium) rs1258777968 Functional Loss SNV dbSNP153 33..33 33 - - - 69997 RMVar_ID_69997 Human_SNP_ID_667863034 m1A Human chr19 - 47781378 47781378 47781378 CCTGTCTAGTGGGCCCCCTCACCTCTGCCTTCAGGGCGCATTAGCCCTGAGCCAAGGCGGCTTTG CCTGTCTAGTGGGCCCCCTCACCTCTGCCTTCGGGGCGCATTAGCCCTGAGCCAAGGCGGCTTTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47781276..47781400 32194978 MeRIP-seq:(Medium) rs756996845 Functional Loss SNV dbSNP153 33..33 33 - - - 69998 RMVar_ID_69998 Human_SNP_ID_667863037 m1A Human chr19 + 47781385 47781385 47781385 GCCTTGGCTCAGGGCTAATGCGCCCTGAAGGCAGAGGTGAGGGGGCCCACTAGACAGGGACACCA GCCTTGGCTCAGGGCTAATGCGCCCTGAAGGCGGAGGTGAGGGGGCCCACTAGACAGGGACACCA A G SELENOW Ensembl:ENSG00000178980 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47781176..47781483 32194978 MeRIP-seq:(Medium) rs1357960489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18998308,Human_RBP_ID_26474217 Human_Splice_Rec_2024740,Human_Splice_Rec_2024741,Human_Splice_Rec_2024750,Human_Splice_Rec_2024751,Human_Splice_Rec_2024760,Human_Splice_Rec_2024761,Human_Splice_Rec_2024770,Human_Splice_Rec_2024771,Human_Splice_Rec_2024778,Human_Splice_Rec_2024779,Human_Splice_Rec_2024788,Human_Splice_Rec_2024796,Human_Splice_Rec_2024797,Human_Splice_Rec_2024808,Human_Splice_Rec_2024809,Human_Splice_Rec_2024820,Human_Splice_Rec_2024821,Human_Splice_Rec_2024824,Human_Splice_Rec_2024828,Human_Splice_Rec_2024829,Human_Splice_Rec_2024832,Human_Splice_Rec_2024833 RMVar_hsa_circ_92059,RMVar_hsa_circ_92650,RMVar_hsa_circ_121685,RMVar_hsa_circ_195623,RMVar_hsa_circ_195624,RMVar_hsa_circ_51673,RMVar_hsa_circ_108085,RMVar_hsa_circ_195625,RMVar_hsa_circ_195626 69999 RMVar_ID_69999 Human_SNP_ID_667940217 m1A Human chr19 - 48074974 48074974 48074974 GGTCACCTGGAGAAGGAGGTCACCTCAGGAGGAACCGCAGGGCATTGCAGAAGATGAGGCAGAGC GGTCACCTGGAGAAGGAGGTCACCTCAGGAGGGACCGCAGGGCATTGCAGAAGATGAGGCAGAGC T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48074966..48075031 26863196 MeRIP-seq:(Medium) rs1389545303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110578,RMVar_hsa_circ_68877,RMVar_hsa_circ_373942,RMVar_hsa_circ_195630,RMVar_hsa_circ_87030,RMVar_hsa_circ_195631,RMVar_hsa_circ_195629 70000 RMVar_ID_70000 Human_SNP_ID_667951473 m1A Human chr19 - 48115961 48115960 48115961 CGCAGGAGTCTCCATCCCGCTTCCGCAGGTGGATAGTGACAAGGGCATCTCCCTTCGCTTCCCTC CGCAGGAGTCTCCATCCCGCTTCCGCAGGTGG_TAGTGACAAGGGCATCTCCCTTCGCTTCCCTC AT A LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48115901..48115975 32194978 MeRIP-seq:(Medium) rs761865488 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2025226,Human_Splice_Rec_2025227,Human_Splice_Rec_2025229,Human_Splice_Rec_2025276,Human_Splice_Rec_2025277,Human_Splice_Rec_2025280,Human_Splice_Rec_2025281,Human_Splice_Rec_2025332,Human_Splice_Rec_2025333,Human_Splice_Rec_2025382,Human_Splice_Rec_2025383,Human_Splice_Rec_2025426,Human_Splice_Rec_2025427,Human_Splice_Rec_2025478,Human_Splice_Rec_2025479,Human_Splice_Rec_2025530,Human_Splice_Rec_2025531 RMVar_hsa_circ_79526,RMVar_hsa_circ_98837,RMVar_hsa_circ_195635,RMVar_hsa_circ_195636 70001 RMVar_ID_70001 Human_SNP_ID_667951476 m1A Human chr19 - 48115961 48115961 48115961 CGCAGGAGTCTCCATCCCGCTTCCGCAGGTGGATAGTGACAAGGGCATCTCCCTTCGCTTCCCTC CGCAGGAGTCTCCATCCCGCTTCCGCAGGTGGGTAGTGACAAGGGCATCTCCCTTCGCTTCCCTC T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48115901..48115975 32194978 MeRIP-seq:(Medium) rs1037193058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2025226,Human_Splice_Rec_2025227,Human_Splice_Rec_2025229,Human_Splice_Rec_2025276,Human_Splice_Rec_2025277,Human_Splice_Rec_2025280,Human_Splice_Rec_2025281,Human_Splice_Rec_2025332,Human_Splice_Rec_2025333,Human_Splice_Rec_2025382,Human_Splice_Rec_2025383,Human_Splice_Rec_2025426,Human_Splice_Rec_2025427,Human_Splice_Rec_2025478,Human_Splice_Rec_2025479,Human_Splice_Rec_2025530,Human_Splice_Rec_2025531 RMVar_hsa_circ_79526,RMVar_hsa_circ_98837,RMVar_hsa_circ_195635,RMVar_hsa_circ_195636 70002 RMVar_ID_70002 Human_SNP_ID_667953700 m1A Human chr19 - 48123284 48123284 48123284 CCTGGTACGTGAGCCCCTTTCCCGGCGCCGGCAGCTGCTCCGGGAGAACTTTGTGGAGACAGAGG CCTGGTACGTGAGCCCCTTTCCCGGCGCCGGCGGCTGCTCCGGGAGAACTTTGTGGAGACAGAGG T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:48123197..48123349 26863196 MeRIP-seq:(Medium) rs1353026647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908825,Human_RBP_ID_4540226 Human_Splice_Rec_2025216,Human_Splice_Rec_2025266,Human_Splice_Rec_2025322,Human_Splice_Rec_2025372,Human_Splice_Rec_2025416,Human_Splice_Rec_2025468,Human_Splice_Rec_2025520,Human_Splice_Rec_2025542 Human_miRNA_ID_2242453 RMVar_hsa_circ_33777,RMVar_hsa_circ_98837,RMVar_hsa_circ_108565,RMVar_hsa_circ_195636,RMVar_hsa_circ_354112,RMVar_hsa_circ_69641,RMVar_hsa_circ_195637,RMVar_hsa_circ_6330,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638 70003 RMVar_ID_70003 Human_SNP_ID_667956381 m1A Human chr19 + 48133035 48133035 48133035 TTTGTATTCGCAGGTGAAAGCTGCCTCCTCAAAGCGTTTCAGGACCTCGCTGATGCCCCGGGTGG TTTGTATTCGCAGGTGAAAGCTGCCTCCTCAAGGCGTTTCAGGACCTCGCTGATGCCCCGGGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48132976..48133135 26863196 MeRIP-seq:(Medium) rs1162053128 Functional Loss SNV dbSNP153 33..33 33 - - - 70004 RMVar_ID_70004 Human_SNP_ID_667956382 m1A Human chr19 + 48133035 48133035 48133035 TTTGTATTCGCAGGTGAAAGCTGCCTCCTCAAAGCGTTTCAGGACCTCGCTGATGCCCCGGGTGG TTTGTATTCGCAGGTGAAAGCTGCCTCCTCAATGCGTTTCAGGACCTCGCTGATGCCCCGGGTGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48132976..48133135 26863196 MeRIP-seq:(Medium) rs1162053128 Functional Loss SNV dbSNP153 33..33 33 - - - 70005 RMVar_ID_70005 Human_SNP_ID_667956644 m1A Human chr19 + 48133940 48133940 48133940 ATGGCCACCCTCACGCCGACTCAGGAGGGAGCAGGGCTGCTGCCAGGCTGGTGAGCGCCCCTGGG ATGGCCACCCTCACGCCGACTCAGGAGGGAGCGGGGCTGCTGCCAGGCTGGTGAGCGCCCCTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48133937..48134013 26863196 MeRIP-seq:(Medium) rs1207523108 Functional Loss SNV dbSNP153 33..33 33 - - - 70006 RMVar_ID_70006 Human_SNP_ID_667956748 m1A Human chr19 - 48134202 48134202 48134202 ACGAAGGGAGAGCACAGAGACAGGGTGGCAAGAGGAGCTTGGCAGGTGGTGACTCAGTGGGCAGA ACGAAGGGAGAGCACAGAGACAGGGTGGCAAGTGGAGCTTGGCAGGTGGTGACTCAGTGGGCAGA T A LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48134200..48134285 26863196 MeRIP-seq:(Medium) rs1039530575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13489524 RMVar_hsa_circ_43196,RMVar_hsa_circ_98837,RMVar_hsa_circ_108565,RMVar_hsa_circ_195636,RMVar_hsa_circ_69641,RMVar_hsa_circ_195637,RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_126693,RMVar_hsa_circ_376509,RMVar_hsa_circ_119674,RMVar_hsa_circ_95771,RMVar_hsa_circ_103030,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,RMVar_hsa_circ_195644,RMVar_hsa_circ_195645,RMVar_hsa_circ_195643,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_104552,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195650,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652 70007 RMVar_ID_70007 Human_SNP_ID_667958437 m1A Human chr19 - 48139905 48139905 48139905 ACAGGAGCTCAGCCAGAGAAAATGCAGAGGTCAGGTGGATCGGAGAGATGGTGGAGAGAGGCTGT ACAGGAGCTCAGCCAGAGAAAATGCAGAGGTCTGGTGGATCGGAGAGATGGTGGAGAGAGGCTGT T A LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48139267..48140025 26863196 MeRIP-seq:(Medium) rs566895594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53358,Human_RBP_ID_13489699,Human_RBP_ID_18736834,Human_RBP_ID_22979623,Human_RBP_ID_23803451,Human_RBP_ID_25428283 RMVar_hsa_circ_43196,RMVar_hsa_circ_108565,RMVar_hsa_circ_195637,RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_376509,RMVar_hsa_circ_119674,RMVar_hsa_circ_95771,RMVar_hsa_circ_103030,RMVar_hsa_circ_86212,RMVar_hsa_circ_4035,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,RMVar_hsa_circ_195644,RMVar_hsa_circ_195643,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_104552,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195650,RMVar_hsa_circ_195651,RMVar_hsa_circ_47166,RMVar_hsa_circ_195652,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653 70008 RMVar_ID_70008 Human_SNP_ID_667961438 m1A Human chr19 - 48150206 48150206 48150206 CATCACCGTCTGAGCTCTCTCACCGCAGAAGCAGAGACCCCGACGGAAAGCGTTTCAGAGCCTGA CATCACCGTCTGAGCTCTCTCACCGCAGAAGCGGAGACCCCGACGGAAAGCGTTTCAGAGCCTGA T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48150055..48150266 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_914964 Human_Splice_Rec_2025188,Human_Splice_Rec_2025238,Human_Splice_Rec_2025294,Human_Splice_Rec_2025344,Human_Splice_Rec_2025388,Human_Splice_Rec_2025440,Human_Splice_Rec_2025492,Human_Splice_Rec_2025572,Human_Splice_Rec_2025590,Human_Splice_Rec_2025598,Human_Splice_Rec_2025606,Human_Splice_Rec_2025616 RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_376509,RMVar_hsa_circ_119674,RMVar_hsa_circ_95771,RMVar_hsa_circ_103030,RMVar_hsa_circ_86212,RMVar_hsa_circ_4035,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,RMVar_hsa_circ_195644,RMVar_hsa_circ_195643,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652,RMVar_hsa_circ_3893,RMVar_hsa_circ_48843,RMVar_hsa_circ_34463,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_83444,RMVar_hsa_circ_195654,RMVar_hsa_circ_295820,RMVar_hsa_circ_304632,RMVar_hsa_circ_317913,RMVar_hsa_circ_62852,RMVar_hsa_circ_195655,RMVar_hsa_circ_195656,RMVar_hsa_circ_195657 70009 RMVar_ID_70009 Human_SNP_ID_667962871 m1A Human chr19 - 48154828 48154828 48154828 AGAGAATGTGGAGTCATGGAAGGGTTTTGAGCAGGGAGAGACAGTGCCAGCCATGCTGATAGAAG AGAGAATGTGGAGTCATGGAAGGGTTTTGAGCCGGGAGAGACAGTGCCAGCCATGCTGATAGAAG T G LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48154826..48154998 26863196 MeRIP-seq:(Medium) rs1194573871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_95771,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_62852,RMVar_hsa_circ_275623 70010 RMVar_ID_70010 Human_SNP_ID_667963207 m1A Human chr19 - 48156133 48156133 48156133 CTGGCGTGTAGAGCGCAGGATTGGGGATGGTGAGCAATGAGGTGAGAAGGTCCTGGAAAACCAGC CTGGCGTGTAGAGCGCAGGATTGGGGATGGTGGGCAATGAGGTGAGAAGGTCCTGGAAAACCAGC T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48156130..48156305 26863196 MeRIP-seq:(Medium) rs990137397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_95771,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_62852,RMVar_hsa_circ_275623 70011 RMVar_ID_70011 Human_SNP_ID_667964732 m1A Human chr19 - 48161452 48161452 48161452 GAGTGGTGTCCGAGAGTGACTCTCCGGTGAAGAGGCCAGGGAGGAAGGCGGCCCGGGTCCTGGGC GAGTGGTGTCCGAGAGTGACTCTCCGGTGAAGGGGCCAGGGAGGAAGGCGGCCCGGGTCCTGGGC T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48161376..48161557 26863196 MeRIP-seq:(Medium) rs1478202640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908826,Human_RBP_ID_3957264,Human_RBP_ID_9381236,Human_RBP_ID_18995227,Human_RBP_ID_22978134,Human_RBP_ID_24545502,Human_RBP_ID_26336518,Human_RBP_ID_27815541 Human_Splice_Rec_2025180,Human_Splice_Rec_2025181,Human_Splice_Rec_2025234,Human_Splice_Rec_2025235,Human_Splice_Rec_2025286,Human_Splice_Rec_2025287,Human_Splice_Rec_2025336,Human_Splice_Rec_2025337,Human_Splice_Rec_2025432,Human_Splice_Rec_2025433,Human_Splice_Rec_2025484,Human_Splice_Rec_2025485,Human_Splice_Rec_2025566,Human_Splice_Rec_2025567,Human_Splice_Rec_2025604,Human_Splice_Rec_2025612,Human_Splice_Rec_2025613,Human_Splice_Rec_2025622,Human_Splice_Rec_2025623,Human_Splice_Rec_2025630 RMVar_hsa_circ_95771,RMVar_hsa_circ_195659,RMVar_hsa_circ_195640,RMVar_hsa_circ_331650,RMVar_hsa_circ_102132,RMVar_hsa_circ_301176,RMVar_hsa_circ_319606,RMVar_hsa_circ_195660 70012 RMVar_ID_70012 Human_SNP_ID_667964982 m1A Human chr19 - 48162317 48162317 48162317 CATTTTTCCACCCCAAGAAAGAGGGTAAAGCAAAGAAGCCTGAGAAGGAGGCATCCAATAGCAGC CATTTTTCCACCCCAAGAAAGAGGGTAAAGCAGAGAAGCCTGAGAAGGAGGCATCCAATAGCAGC T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48162216..48162399 26863196 MeRIP-seq:(Medium) rs773651278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955320,Human_RBP_ID_4540298,Human_RBP_ID_9381238,Human_RBP_ID_18998334,Human_RBP_ID_22974932,Human_RBP_ID_26334941,Human_RBP_ID_26992911,Human_RBP_ID_27815543 Human_Splice_Rec_2025178,Human_Splice_Rec_2025179,Human_Splice_Rec_2025232,Human_Splice_Rec_2025233,Human_Splice_Rec_2025284,Human_Splice_Rec_2025285,Human_Splice_Rec_2025430,Human_Splice_Rec_2025431,Human_Splice_Rec_2025482,Human_Splice_Rec_2025483,Human_Splice_Rec_2025564,Human_Splice_Rec_2025565,Human_Splice_Rec_2025602,Human_Splice_Rec_2025603,Human_Splice_Rec_2025610,Human_Splice_Rec_2025611,Human_Splice_Rec_2025620,Human_Splice_Rec_2025621,Human_Splice_Rec_2025628,Human_Splice_Rec_2025629,Human_Splice_Rec_2025634 RMVar_hsa_circ_95771,RMVar_hsa_circ_195640,RMVar_hsa_circ_331650,RMVar_hsa_circ_301176,RMVar_hsa_circ_319606,RMVar_hsa_circ_195660 70013 RMVar_ID_70013 Human_SNP_ID_667967405 m1A Human chr19 + 48170291 48170291 48170291 GCCGCTGCCCGGGCAACACACTCAGATCCGCCAGGCGCGCCTCTGCAGTCCCAAGTTCGCGCCAC GCCGCTGCCCGGGCAACACACTCAGATCCGCCGGGCGCGCCTCTGCAGTCCCAAGTTCGCGCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48170183..48170350;chr19:48169972..48170350;chr19:48169965..48170350;chr19:48170060..48170350 26863196 MeRIP-seq:(Medium) rs1310468475 Functional Loss SNV dbSNP153 33..33 33 - - - 70014 RMVar_ID_70014 Human_SNP_ID_667967720 m1A Human chr19 - 48171247 48171247 48171247 ACGGACCCCTCACCCGGTCACATGCTTCATGCACCTGTGGCTCCGCACTCCCCAGATGTGCCTCT ACGGACCCCTCACCCGGTCACATGCTTCATGCTCCTGTGGCTCCGCACTCCCCAGATGTGCCTCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48171076..48171317 32194978 MeRIP-seq:(Medium) rs891788605 Functional Loss SNV dbSNP153 33..33 33 - - - 70015 RMVar_ID_70015 Human_SNP_ID_667967885 m1A Human chr19 + 48171864 48171864 48171864 GGCTGCGGGGCAGGAGGAGCAGGAGCTGCGGGAGCGGGCCTTCTTCTCGTGGGCCGAGTTCAGCC GGCTGCGGGGCAGGAGGAGCAGGAGCTGCGGGGGCGGGCCTTCTTCTCGTGGGCCGAGTTCAGCC A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48171792..48171863 26863196 MeRIP-seq:(Medium) rs1404496757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17928844,Human_RBP_ID_22978137 Human_Splice_Rec_2025648,Human_Splice_Rec_2025654 70016 RMVar_ID_70016 Human_SNP_ID_667970421 m1A Human chr19 + 48182637 48182635 48182638 CAACGCCTGCCTGCCGGTGCGCACCACCAACAAGATCTCCAAGCAGTTCGTGGCCCCAGCCGACG CAACGCCTGCCTGCCGGTGCGCACCACCAAC___ATCTCCAAGCAGTTCGTGGCCCCAGCCGACG CAAG C ZSWIM9 Ensembl:ENSG00000185453 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48182425..48182700 26863196 MeRIP-seq:(Medium) rs1017067324 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_337782 70017 RMVar_ID_70017 Human_SNP_ID_667970894 m1A Human chr19 + 48184050 48184050 48184050 AATGTTCTCAAGGGGAGAACACACCTGAACCCACCATGCAGATGGAGAATTAGGAGAAGGAAGAG AATGTTCTCAAGGGGAGAACACACCTGAACCCTCCATGCAGATGGAGAATTAGGAGAAGGAAGAG A T ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48184040..48184293 26863196 MeRIP-seq:(Medium) rs952486569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13490319 70018 RMVar_ID_70018 Human_SNP_ID_667974428 m1A Human chr19 - 48195694 48195694 48195694 TGGCCCTCTCAGGTGCCCTTTCTCTAACTTCGACCCTCTCAAGACACCCCCTTCCAGTCCCCTCG TGGCCCTCTCAGGTGCCCTTTCTCTAACTTCGGCCCTCTCAAGACACCCCCTTCCAGTCCCCTCG T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48195340..48196782 26863196 MeRIP-seq:(Medium) rs1199274556 Functional Loss SNV dbSNP153 33..33 33 - - - 70019 RMVar_ID_70019 Human_SNP_ID_667974431 m1A Human chr19 + 48195697 48195697 48195697 GGGGACTGGAAGGGGGTGTCTTGAGAGGGTCGAAGTTAGAGAAAGGGCACCTGAGAGGGCCAGAG GGGGACTGGAAGGGGGTGTCTTGAGAGGGTCGCAGTTAGAGAAAGGGCACCTGAGAGGGCCAGAG A C ZSWIM9 Ensembl:ENSG00000185453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48195343..48196891 26863196 MeRIP-seq:(Medium) rs1338972098 Functional Loss SNV dbSNP153 33..33 33 - - - 70020 RMVar_ID_70020 Human_SNP_ID_667974585 m1A Human chr19 + 48196291 48196291 48196291 ATGGAGGGGGAGCCCGGTCCGTGGGCCCCAAGAGCCGAGCCGGACGAGGGATGGAGTGGGGAGAC ATGGAGGGGGAGCCCGGTCCGTGGGCCCCAAGGGCCGAGCCGGACGAGGGATGGAGTGGGGAGAC A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:48196026..48196415 26863196 MeRIP-seq:(Medium) rs1393873675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6777329,Human_RBP_ID_17928856 70021 RMVar_ID_70021 Human_SNP_ID_667974693 m1A Human chr19 + 48196667 48196667 48196667 AGCTGGCTTTGCCCTTAAGGACGGCACCTCGGACTTCTTCCTGGATGGGGCCCTGACACGCTGCA AGCTGGCTTTGCCCTTAAGGACGGCACCTCGGTCTTCTTCCTGGATGGGGCCCTGACACGCTGCA A T ZSWIM9 Ensembl:ENSG00000185453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48196385..48196880 32194978 MeRIP-seq:(Medium) rs532738292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017380,Human_RBP_ID_1569121,Human_RBP_ID_6777331,Human_RBP_ID_27469967 70022 RMVar_ID_70022 Human_SNP_ID_667974881 m1A Human chr19 + 48197303 48197303 48197303 TAAGCGAGAAAAAATGGAAAGGGGAGCCGGAAATGGAGGAGAGAGGACAAGCAAAGAGACAGAAA TAAGCGAGAAAAAATGGAAAGGGGAGCCGGAAGTGGAGGAGAGAGGACAAGCAAAGAGACAGAAA A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:48197016..48197407 26863196 MeRIP-seq:(Medium) rs1182170191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264032,Human_RBP_ID_524699,Human_RBP_ID_24552867 70023 RMVar_ID_70023 Human_SNP_ID_667976500 m1A Human chr19 + 48203904 48203904 48203904 GTATCTCCTGCTGTAGCAGCCAGAAAGCTACAACTCCCAGCCGGCTGAGCGCCACCAGCGCTTTC GTATCTCCTGCTGTAGCAGCCAGAAAGCTACATCTCCCAGCCGGCTGAGCGCCACCAGCGCTTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48203810..48203944 26863196 MeRIP-seq:(Medium) rs1399594950 Functional Loss SNV dbSNP153 33..33 33 - - - 70024 RMVar_ID_70024 Human_SNP_ID_667976509 m1A Human chr19 + 48203919 48203919 48203919 GCAGCCAGAAAGCTACAACTCCCAGCCGGCTGAGCGCCACCAGCGCTTTCGCGTCCAAGTCCCTT GCAGCCAGAAAGCTACAACTCCCAGCCGGCTGGGCGCCACCAGCGCTTTCGCGTCCAAGTCCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48203830..48203939 26863196 MeRIP-seq:(Medium) rs1324350749 Functional Loss SNV dbSNP153 33..33 33 - - - 70025 RMVar_ID_70025 Human_SNP_ID_667976663 m1A Human chr19 + 48204268 48204268 48204268 CAGTAACCCTGGAGTGGAAGGAGACGGGGATTAGAGACCTCGCGGGAGAAATTAGACTAACAGCC CAGTAACCCTGGAGTGGAAGGAGACGGGGATTTGAGACCTCGCGGGAGAAATTAGACTAACAGCC A T AC011466.1 Ensembl:ENSG00000268583 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48204229..48204330 26863196 MeRIP-seq:(Medium) rs1321342374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587180 70026 RMVar_ID_70026 Human_SNP_ID_668009393 m1A Human chr19 - 48325595 48325595 48325595 ACGGACTGGAAACTTACCGAGAGCCGCGAAAAAAGTCAGAGCTGGAGTCGGAGTCTTGTCCCTCG ACGGACTGGAAACTTACCGAGAGCCGCGAAAACAGTCAGAGCTGGAGTCGGAGTCTTGTCCCTCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48325315..48326974 26863196 MeRIP-seq:(Medium) rs944350066 Functional Loss SNV dbSNP153 33..33 33 - - - 70027 RMVar_ID_70027 Human_SNP_ID_668009883 m1A Human chr19 - 48327532 48327530 48327532 TACCAGAGATTCAGGGACTCTTTCCCAGGGAGAGTCCACCAGGACTGGGATGGACAGAGAACGAA TACCAGAGATTCAGGGACTCTTTCCCAGGGAG__TCCACCAGGACTGGGATGGACAGAGAACGAA ACT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48326019..48327600 32194978 MeRIP-seq:(Medium) rs768347751 Functional Loss DEL dbSNP153 33..34 33 - - - 70028 RMVar_ID_70028 Human_SNP_ID_668009897 m1A Human chr19 - 48327569 48327569 48327569 GGCCCATGTTTTGGTGTCGTTGTTCCACGTGCAGTCGTACCAGAGATTCAGGGACTCTTTCCCAG GGCCCATGTTTTGGTGTCGTTGTTCCACGTGCGGTCGTACCAGAGATTCAGGGACTCTTTCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:48327501..48327600;chr19:48327501..48327575 26863196 MeRIP-seq:(Medium) rs1476209533 Functional Loss SNV dbSNP153 33..33 33 - - - 70029 RMVar_ID_70029 Human_SNP_ID_668010337 m1A Human chr19 - 48329385 48329385 48329385 GGATGAAGGAGAGACAGCAGAGAATGAGGGAGAGCACCATGAGGACCTGCACCGCCTTCAGCCAG GGATGAAGGAGAGACAGCAGAGAATGAGGGAGCGCACCATGAGGACCTGCACCGCCTTCAGCCAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48329376..48329400 26863196 MeRIP-seq:(Medium) rs1569018284 Functional Loss SNV dbSNP153 33..33 33 - - - 70030 RMVar_ID_70030 Human_SNP_ID_668010679 m1A Human chr19 + 48330445 48330445 48330445 CTTCCCCCTCGCCCTGGTCAGCGGCATCATCTACATCCACCTACGGAAGCGGGAGTGAGCGCCCC CTTCCCCCTCGCCCTGGTCAGCGGCATCATCTGCATCCACCTACGGAAGCGGGAGTGAGCGCCCC A G EMP3 Ensembl:ENSG00000142227 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48330268..48330550 26863196 MeRIP-seq:(Medium) rs778634607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524779,Human_RBP_ID_17928907,Human_RBP_ID_22533446,Human_RBP_ID_22764764,Human_RBP_ID_27469989 RMVar_hsa_circ_99095,RMVar_hsa_circ_195676 70031 RMVar_ID_70031 Human_SNP_ID_668011461 m1A Human chr19 - 48333227 48333227 48333227 CCGAGCCCCCGCAAGCCACGCCCAGCAGTAACATCTCCTGAGTAGAACCTACCTCCCTGCCCAGT CCGAGCCCCCGCAAGCCACGCCCAGCAGTAACGTCTCCTGAGTAGAACCTACCTCCCTGCCCAGT T C TMEM143 Ensembl:ENSG00000161558 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48333181..48333305 26863196 MeRIP-seq:(Medium) rs1431825088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2691102,Human_miRNA_ID_2771352 RMVar_hsa_circ_195677,RMVar_hsa_circ_78870,RMVar_hsa_circ_126562,RMVar_hsa_circ_83007,RMVar_hsa_circ_195678,RMVar_hsa_circ_195679 70032 RMVar_ID_70032 Human_SNP_ID_668020243 m1A Human chr19 + 48364010 48364010 48364010 CAGCAGTAAAACGCATGCGCAAAGCTTCGGTCAATGCGGGCTGTCCATTTCTCACCGCCGACTCC CAGCAGTAAAACGCATGCGCAAAGCTTCGGTCCATGCGGGCTGTCCATTTCTCACCGCCGACTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48363960..48364116 26863196 MeRIP-seq:(Medium) rs1215253307 Functional Loss SNV dbSNP153 33..33 33 - - - 70033 RMVar_ID_70033 Human_SNP_ID_668025372 m1A Human chr19 + 48382749 48382748 48382749 CAGGAGAAGACCAAAAAATTCAAACTCTGGGGAAAAAAATTACTATGAAAAAAAATCAGGGGAGA CAGGAGAAGACCAAAAAATTCAAACTCTGGGG_AAAAAATTACTATGAAAAAAAATCAGGGGAGA GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48382699..48382937 26863196 MeRIP-seq:(Medium) rs889036713 Functional Loss DEL dbSNP153 33..33 33 - - - 70034 RMVar_ID_70034 Human_SNP_ID_668025374 m1A Human chr19 + 48382749 48382749 48382749 CAGGAGAAGACCAAAAAATTCAAACTCTGGGGAAAAAAATTACTATGAAAAAAAATCAGGGGAGA CAGGAGAAGACCAAAAAATTCAAACTCTGGGGGAAAAAATTACTATGAAAAAAAATCAGGGGAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48382699..48382937 26863196 MeRIP-seq:(Medium) rs184579639 Functional Loss SNV dbSNP153 33..33 33 - - - 70035 RMVar_ID_70035 Human_SNP_ID_668025399 m1A Human chr19 - 48382844 48382844 48382844 GACACCCATCTGCCCCACCTCCTGCCATGGCCATGAACCGCGACCCCCACTAAATTTCTAGATTG GACACCCATCTGCCCCACCTCCTGCCATGGCCGTGAACCGCGACCCCCACTAAATTTCTAGATTG T C KDELR1 Ensembl:ENSG00000105438 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:48382793..48382968;chr19:48382749..48382866 26863196 MeRIP-seq:(Medium) rs1315551430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_524815,Human_RBP_ID_4540579,Human_RBP_ID_6777559,Human_RBP_ID_8197892,Human_RBP_ID_8491424,Human_RBP_ID_13490950,Human_RBP_ID_17386931,Human_RBP_ID_17502634,Human_RBP_ID_17657245,Human_RBP_ID_17928925,Human_RBP_ID_26469472 Human_miRNA_ID_878327,Human_miRNA_ID_1810745 70036 RMVar_ID_70036 Human_SNP_ID_668025449 m1A Human chr19 + 48383027 48383027 48383027 ACTTTATAAAAATTGGGGCCACAGAGTAGAAGAAAAACGAGTCATCAGAATCAAAAACTAAAGAG ACTTTATAAAAATTGGGGCCACAGAGTAGAAGGAAAACGAGTCATCAGAATCAAAAACTAAAGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48382651..48383050 32194978 MeRIP-seq:(Medium) rs1487832262 Functional Loss SNV dbSNP153 33..33 33 - - - 70037 RMVar_ID_70037 Human_SNP_ID_668025506 m1A Human chr19 - 48383250 48383250 48383250 CTCCATCTCTCTCCTCGGCAGCAGCGGGAGGCAGAGGAAGGCGGCAGAAGATGAAGAGCTTTCCC CTCCATCTCTCTCCTCGGCAGCAGCGGGAGGCGGAGGAAGGCGGCAGAAGATGAAGAGCTTTCCC T C KDELR1 Ensembl:ENSG00000105438 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48383076..48383350 32194978 MeRIP-seq:(Medium) rs1383665652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55140,Human_RBP_ID_524817,Human_RBP_ID_773682,Human_RBP_ID_4571430,Human_RBP_ID_6777589,Human_RBP_ID_13490998,Human_RBP_ID_17502470,Human_RBP_ID_18192364,Human_RBP_ID_22446902,Human_RBP_ID_22764206,Human_RBP_ID_27276656 Human_Splice_Rec_2026490,Human_Splice_Rec_2026496 70038 RMVar_ID_70038 Human_SNP_ID_668025742 m1A Human chr19 + 48384326 48384326 48384326 GGCGATGAGGTCGAAGAAGCCCTCGAAATGGTAGCGCCAGATCCAGTTGAAGAGATAGAGCGTGC GGCGATGAGGTCGAAGAAGCCCTCGAAATGGTGGCGCCAGATCCAGTTGAAGAGATAGAGCGTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48384226..48384325 32194978 MeRIP-seq:(Medium) rs369566600 Functional Loss SNV dbSNP153 33..33 33 - - - 70039 RMVar_ID_70039 Human_SNP_ID_668027788 m1A Human chr19 - 48391412 48391412 48391412 GCTACCCGTTCAGACCAGCAGCCTCGGGGGGCACCCCCCCGCCAGCCTGCCTCCCTCCCGCTCAG GCTACCCGTTCAGACCAGCAGCCTCGGGGGGCCCCCCCCCGCCAGCCTGCCTCCCTCCCGCTCAG T G KDELR1 Ensembl:ENSG00000105438 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr19:48391238..48391575;chr19:48391251..48391575;chr19:48391321..48391542 26863410 MeRIP-seq:(Medium) rs969804610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241380,Human_RBP_ID_524863,Human_RBP_ID_773684,Human_RBP_ID_4558629,Human_RBP_ID_5130553,Human_RBP_ID_17271920,Human_RBP_ID_17386954,Human_RBP_ID_18947177,Human_RBP_ID_22447916,Human_RBP_ID_22533187,Human_RBP_ID_27276669 70040 RMVar_ID_70040 Human_SNP_ID_668028002 m1A Human chr19 - 48392120 48392120 48392120 GAGGAGGCTGGGGGCCTGGACTCCTGGGTCTGAGCGAGGAGGAGCTGGGCCTGGACTCCTGGATC GAGGAGGCTGGGGGCCTGGACTCCTGGGTCTGGGCGAGGAGGAGCTGGGCCTGGACTCCTGGATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48391971..48392296 26863196 MeRIP-seq:(Medium) rs935287934 Functional Loss SNV dbSNP153 33..33 33 - - - 70041 RMVar_ID_70041 Human_SNP_ID_668028938 m1A Human chr19 - 48394992 48394992 48394992 CCACGAGGCTTCTTGCCAACTTCCTCTGTCCTAGATTTGGGGGTCCACATTCCCACCACCATCCC CCACGAGGCTTCTTGCCAACTTCCTCTGTCCTGGATTTGGGGGTCCACATTCCCACCACCATCCC T C lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48394956..48395369 26863196 MeRIP-seq:(Medium) rs1445149220 Functional Loss SNV dbSNP153 33..33 33 - - - 70042 RMVar_ID_70042 Human_SNP_ID_668029282 m1A Human chr19 - 48396194 48396194 48396194 CCTCAGGGATCACAGAGTCCAGCCTCTGGACAACCCCCCGCTCCCCCCGCCTCCATCTCTACCTC CCTCAGGGATCACAGAGTCCAGCCTCTGGACACCCCCCCGCTCCCCCCGCCTCCATCTCTACCTC T G lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:48396108..48396284 26863196 MeRIP-seq:(Medium) rs886805960 Functional Loss SNV dbSNP153 33..33 33 - - - 70043 RMVar_ID_70043 Human_SNP_ID_668029703 m1A Human chr19 - 48397741 48397739 48397742 GGGAGACGGGGAGGGAAAGAGCGGCAGGAAGAAGGAGAGAGACGGAAGCAGCAGAGACGGGGAGA GGGAGACGGGGAGGGAAAGAGCGGCAGGAAG___GAGAGAGACGGAAGCAGCAGAGACGGGGAGA CCTT C lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:48397476..48398350 26863196 MeRIP-seq:(Medium) rs1228002053 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17068395 70044 RMVar_ID_70044 Human_SNP_ID_668029704 m1A Human chr19 - 48397741 48397741 48397741 GGGAGACGGGGAGGGAAAGAGCGGCAGGAAGAAGGAGAGAGACGGAAGCAGCAGAGACGGGGAGA GGGAGACGGGGAGGGAAAGAGCGGCAGGAAGAGGGAGAGAGACGGAAGCAGCAGAGACGGGGAGA T C lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:48397476..48398350 26863196 MeRIP-seq:(Medium) rs924876967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17068395 70045 RMVar_ID_70045 Human_SNP_ID_668029800 m1A Human chr19 - 48398147 48398146 48398148 GATGGAAGGGAGAGAGACAGAGGGAGAGAGAAATGGAGGAGAGACAGAGGGAGAGACGGGCAGAG GATGGAAGGGAGAGAGACAGAGGGAGAGAGA__TGGAGGAGAGACAGAGGGAGAGACGGGCAGAG ATT A lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:48398024..48398200 26863196 MeRIP-seq:(Medium) rs1263431236 Functional Loss DEL dbSNP153 32..33 33 - - - 70046 RMVar_ID_70046 Human_SNP_ID_668029846 m1A Human chr19 - 48398323 48398323 48398323 GGCCGGGAGAGACGGGGAGGAGAGGGAGGCACAGACGGGAGACGCAGGGACAGGGAGACGAGATA GGCCGGGAGAGACGGGGAGGAGAGGGAGGCACCGACGGGAGACGCAGGGACAGGGAGACGAGATA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:48397965..48398446 26863196 MeRIP-seq:(Medium) rs1444063459 Functional Loss SNV dbSNP153 33..33 33 - - - 70047 RMVar_ID_70047 Human_SNP_ID_668033376 m1A Human chr19 - 48410662 48410662 48410662 AGAGGCGTCTTTCTATACCCAAAACTCACGCCACCCGTCTCCTGCTCATAACCCACCCCTGGCTC AGAGGCGTCTTTCTATACCCAAAACTCACGCCGCCCGTCTCCTGCTCATAACCCACCCCTGGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48410658..48410805 26863196 MeRIP-seq:(Medium) rs1486091291 Functional Loss SNV dbSNP153 33..33 33 - - - 70048 RMVar_ID_70048 Human_SNP_ID_668043119 m1A Human chr19 + 48446050 48446050 48446050 AAGGGTCGGCGGCGCACGTGTGAAACCGGGGAACCCATGGAAGCCGAGTCCGGCGACACAAGTTC AAGGGTCGGCGGCGCACGTGTGAAACCGGGGAGCCCATGGAAGCCGAGTCCGGCGACACAAGTTC A G GRWD1 Ensembl:ENSG00000105447 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:48446001..48446225;chr19:48446001..48446175 26863196 MeRIP-seq:(Medium) rs1211406254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1890714,Human_RBP_ID_4540653,Human_RBP_ID_9381246,Human_RBP_ID_24552949,Human_RBP_ID_26336524 RMVar_hsa_circ_195690,RMVar_hsa_circ_377229 70049 RMVar_ID_70049 Human_SNP_ID_668044616 m1A Human chr19 - 48450752 48450752 48450752 CAGGTCCTCCACAGAGCGTGTGTGGCCCACGAATGGCCGCTGGTCCACGTGCCAGGAGCCGCCGT CAGGTCCTCCACAGAGCGTGTGTGGCCCACGAGTGGCCGCTGGTCCACGTGCCAGGAGCCGCCGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48450701..48452949 32194978 MeRIP-seq:(Medium) rs1285411761 Functional Loss SNV dbSNP153 33..33 33 - - - 70050 RMVar_ID_70050 Human_SNP_ID_668045574 m1A Human chr19 - 48453742 48453742 48453742 CCAAACCCAGCTGGCAGGAAGACAACGGGCAGAAGCAAATTGTGTTGGAGGAACCCACACCTCCA CCAAACCCAGCTGGCAGGAAGACAACGGGCAGGAGCAAATTGTGTTGGAGGAACCCACACCTCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48453693..48453843 32194978 MeRIP-seq:(Medium) rs752735908 Functional Loss SNV dbSNP153 33..33 33 - - - 70051 RMVar_ID_70051 Human_SNP_ID_668049695 m1A Human chr19 + 48468141 48468141 48468141 GAAAAAAGGCCTCTGAGATGGGAGAAGGAATCAGAGAGGTGGGAGGATGCTGAGGAAAGGGGAGT GAAAAAAGGCCTCTGAGATGGGAGAAGGAATCGGAGAGGTGGGAGGATGCTGAGGAAAGGGGAGT A G AC008403.1 Ensembl:ENSG00000268465 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48468094..48468205 26863196 MeRIP-seq:(Medium) rs113705584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6777854 70052 RMVar_ID_70052 Human_SNP_ID_668050072 m1A Human chr19 + 48469358 48469357 48469359 CCTACTGAAGGGGCGGTTGGGCGACGAAGGGAAGAGTCTTTTCAGCGCTGAGGACTGGCGCTGAG CCTACTGAAGGGGCGGTTGGGCGACGAAGGGA__AGTCTTTTCAGCGCTGAGGACTGGCGCTGAG AAG A CYTH2,AC008403.1 Ensembl:ENSG00000105443,Ensembl:ENSG00000268465 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48469261..48469687 26863196 MeRIP-seq:(Medium) rs964347474 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_770873,Human_RBP_ID_826106,Human_RBP_ID_18420960,Human_RBP_ID_18737023,Human_RBP_ID_26336527 RMVar_hsa_circ_195692,RMVar_hsa_circ_116903 70053 RMVar_ID_70053 Human_SNP_ID_668050074 m1A Human chr19 + 48469358 48469358 48469358 CCTACTGAAGGGGCGGTTGGGCGACGAAGGGAAGAGTCTTTTCAGCGCTGAGGACTGGCGCTGAG CCTACTGAAGGGGCGGTTGGGCGACGAAGGGAGGAGTCTTTTCAGCGCTGAGGACTGGCGCTGAG A G CYTH2,AC008403.1 Ensembl:ENSG00000105443,Ensembl:ENSG00000268465 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48469261..48469687 26863196 MeRIP-seq:(Medium) rs1287622935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770873,Human_RBP_ID_826106,Human_RBP_ID_18420960,Human_RBP_ID_18737023,Human_RBP_ID_26336527 RMVar_hsa_circ_195692,RMVar_hsa_circ_116903 70054 RMVar_ID_70054 Human_SNP_ID_668050090 m1A Human chr19 - 48469387 48469387 48469387 TCAAACGCCCCGGGAGCCACCGCCGCCTCCTCAGCGCCAGTCCTCAGCGCTGAAAAGACTCTTCC TCAAACGCCCCGGGAGCCACCGCCGCCTCCTCGGCGCCAGTCCTCAGCGCTGAAAAGACTCTTCC T C AC008403.2 Ensembl:ENSG00000268530 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:48469272..48469573;chr19:48469278..48469637;chr19:48469344..48469575 26863196 MeRIP-seq:(Medium) rs1555897777 Functional Loss SNV dbSNP153 33..33 33 - - - 70055 RMVar_ID_70055 Human_SNP_ID_668050091 m1A Human chr19 + 48469389 48469387 48469390 AAGAGTCTTTTCAGCGCTGAGGACTGGCGCTGAGGAGGCGGCGGTGGCTCCCGGGGCGTTTGAGC AAGAGTCTTTTCAGCGCTGAGGACTGGCGCT___GAGGCGGCGGTGGCTCCCGGGGCGTTTGAGC TGAG T CYTH2,AC008403.1 Ensembl:ENSG00000105443,Ensembl:ENSG00000268465 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48469264..48469687 26863196 MeRIP-seq:(Medium) rs1569086449 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4559783,Human_RBP_ID_17929018,Human_RBP_ID_18420960,Human_RBP_ID_18441756,Human_RBP_ID_26336527 RMVar_hsa_circ_195692,RMVar_hsa_circ_116903 70056 RMVar_ID_70056 Human_SNP_ID_668051561 m1A Human chr19 - 48473998 48473998 48473998 TTGGGGCCCGCACCTGTGGACTGGAAAACCCCAGGGTTGCACAGGCAGTATCGCTGGGCGAAGGC TTGGGGCCCGCACCTGTGGACTGGAAAACCCCGGGGTTGCACAGGCAGTATCGCTGGGCGAAGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48473951..48474025 32194978 MeRIP-seq:(Medium) rs1462220723 Functional Loss SNV dbSNP153 33..33 33 - - - 70057 RMVar_ID_70057 Human_SNP_ID_668051672 m1A Human chr19 - 48474273 48474273 48474273 CCGCCCTCGTTGATGCCCCGGTTCATGGCCACAAAGCGCTCCAGGCCCGGCTTGTCCCGGACATT CCGCCCTCGTTGATGCCCCGGTTCATGGCCACGAAGCGCTCCAGGCCCGGCTTGTCCCGGACATT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48474223..48474349 26863196 MeRIP-seq:(Medium) rs138838239 Functional Loss SNV dbSNP153 33..33 33 - - - 70058 RMVar_ID_70058 Human_SNP_ID_668053370 m1A Human chr19 - 48479216 48479215 48479216 GCAGCTCCGTAATAAATAATGGAGTTGGGGGCAGGGGGTCAGGGCTGCTCCTGCTTCTTCTTGAC GCAGCTCCGTAATAAATAATGGAGTTGGGGGC_GGGGGTCAGGGCTGCTCCTGCTTCTTCTTGAC CT C lnc-LMTK3-1 RNACentral:URS00008B77CE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48479170..48479333 26863196 MeRIP-seq:(Medium) rs762239245 Functional Loss DEL dbSNP153 33..33 33 - - - 70059 RMVar_ID_70059 Human_SNP_ID_668053536 m1A Human chr19 - 48479769 48479769 48479769 CCAGCTCCAGGTTGTCCTCAAAGCCCTGGCCCAGCTCACAACCTCACCAGCTTCATCTCCTGCCC CCAGCTCCAGGTTGTCCTCAAAGCCCTGGCCCGGCTCACAACCTCACCAGCTTCATCTCCTGCCC T C lnc-LMTK3-1 RNACentral:URS00008B77CE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48479719..48479897 26863196 MeRIP-seq:(Medium) rs1016502384 Functional Loss SNV dbSNP153 33..33 33 - - - 70060 RMVar_ID_70060 Human_SNP_ID_668053909 m1A Human chr19 + 48480869 48480869 48480869 TTTCCTGCCGCCTCCCCGGATGAACTGCATGCAGGGCGGCCGGCTCCGTGGCAGGCAGAGGCAGG TTTCCTGCCGCCTCCCCGGATGAACTGCATGCTGGGCGGCCGGCTCCGTGGCAGGCAGAGGCAGG A T CYTH2 Ensembl:ENSG00000105443 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48480821..48480901 26863196 MeRIP-seq:(Medium) rs1462259400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21978118,Human_RBP_ID_23803798 Human_miRNA_ID_2381567,Human_miRNA_ID_3024577 RMVar_hsa_circ_86796,RMVar_hsa_circ_195694 70061 RMVar_ID_70061 Human_SNP_ID_668053985 m1A Human chr19 + 48481070 48481070 48481070 AAGGGCAGGAGGCAGGGGCCTGACGTGTTTGGATTGAGGTTGCAGGAGGGGCCCCTGGCTGCTTC AAGGGCAGGAGGCAGGGGCCTGACGTGTTTGGGTTGAGGTTGCAGGAGGGGCCCCTGGCTGCTTC A G CYTH2 Ensembl:ENSG00000105443 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48481019..48481219 32194978 MeRIP-seq:(Medium) rs1050339676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6777897,Human_RBP_ID_13491935,Human_RBP_ID_22979642,Human_RBP_ID_23803800,Human_RBP_ID_25428911 RMVar_hsa_circ_86796,RMVar_hsa_circ_195694 70062 RMVar_ID_70062 Human_SNP_ID_668053987 m1A Human chr19 - 48481077 48481077 48481077 TCTCCCTGAAGCAGCCAGGGGCCCCTCCTGCAACCTCAATCCAAACACGTCAGGCCCCTGCCTCC TCTCCCTGAAGCAGCCAGGGGCCCCTCCTGCAGCCTCAATCCAAACACGTCAGGCCCCTGCCTCC T C lnc-LMTK3-1 RNACentral:URS00008B77CE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48480720..48481235;chr19:48480714..48481252 26863196 MeRIP-seq:(Medium) rs541527943 Functional Loss SNV dbSNP153 33..33 33 - - - 70063 RMVar_ID_70063 Human_SNP_ID_668053988 m1A Human chr19 - 48481077 48481077 48481077 TCTCCCTGAAGCAGCCAGGGGCCCCTCCTGCAACCTCAATCCAAACACGTCAGGCCCCTGCCTCC TCTCCCTGAAGCAGCCAGGGGCCCCTCCTGCACCCTCAATCCAAACACGTCAGGCCCCTGCCTCC T G lnc-LMTK3-1 RNACentral:URS00008B77CE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48480720..48481235;chr19:48480714..48481252 26863196 MeRIP-seq:(Medium) rs541527943 Functional Loss SNV dbSNP153 33..33 33 - - - 70064 RMVar_ID_70064 Human_SNP_ID_668055257 m1A Human chr19 + 48485440 48485440 48485440 CTGCGGCCCCTGTCTTGGGCCAGGAGTGGGTGAGGAGGGACCTCCGCTGTGTCGAGGGGCTCCAG CTGCGGCCCCTGTCTTGGGCCAGGAGTGGGTGGGGAGGGACCTCCGCTGTGTCGAGGGGCTCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48485399..48485519 26863196 MeRIP-seq:(Medium) rs1276940903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6777927 70065 RMVar_ID_70065 Human_SNP_ID_668055395 m1A Human chr19 - 48485764 48485764 48485764 TCCTCAGGCCCCGTGGAGAATTGATTCCCCGAAGACCCGACCCCGCTGCACCCTCAGAAGAGGGG TCCTCAGGCCCCGTGGAGAATTGATTCCCCGAGGACCCGACCCCGCTGCACCCTCAGAAGAGGGG T C LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48485717..48491492 26863196 MeRIP-seq:(Medium) rs1316800238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2026750,Human_Splice_Rec_2026766,Human_Splice_Rec_2026794,Human_Splice_Rec_2026824,Human_Splice_Rec_2026854,Human_Splice_Rec_2026884 70066 RMVar_ID_70066 Human_SNP_ID_668057250 m1A Human chr19 - 48491938 48491938 48491938 GCATCCAGCACGGCATGCGCTCAGGATGGGGCAGGGGTTGGGAGGGCCACTGGAGCAGGTCAAGA GCATCCAGCACGGCATGCGCTCAGGATGGGGCGGGGGTTGGGAGGGCCACTGGAGCAGGTCAAGA T C LMTK3 Ensembl:ENSG00000142235 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48491932..48492016 26863196 MeRIP-seq:(Medium) rs1367417736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70067 RMVar_ID_70067 Human_SNP_ID_668057482 m1A Human chr19 - 48492797 48492797 48492797 TCTGGAGAGAGAGTGTGGGTCTGGAAGGAAAGAGGGGGTACTGGGTAGTCAAGTATGGGATCCTG TCTGGAGAGAGAGTGTGGGTCTGGAAGGAAAGGGGGGGTACTGGGTAGTCAAGTATGGGATCCTG T C LMTK3 Ensembl:ENSG00000142235 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:48492679..48492923 26863196 MeRIP-seq:(Medium) rs533649594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9427531,Human_RBP_ID_23803810 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70068 RMVar_ID_70068 Human_SNP_ID_668057541 m1A Human chr19 - 48493028 48493027 48493028 GGGCGGATGGAGCAGGGCGCGGGAAGGGCCTGAGGGGTGAAGGCGGGGTCTGGGGAGAGACTGGT GGGCGGATGGAGCAGGGCGCGGGAAGGGCCTG_GGGGTGAAGGCGGGGTCTGGGGAGAGACTGGT CT C LMTK3 Ensembl:ENSG00000142235 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48492978..48493078 26863196 MeRIP-seq:(Medium) rs1391752787 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8196758 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70069 RMVar_ID_70069 Human_SNP_ID_668057906 m1A Human chr19 - 48493962 48493962 48493962 GGCCGGCGGGGCGGGAGCGCCGGGGCCGGCGGAGGAGGACGGGGAGGACGAGGACGAGGACGAGG GGCCGGCGGGGCGGGAGCGCCGGGGCCGGCGGCGGAGGACGGGGAGGACGAGGACGAGGACGAGG T G LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48493584..48497626 26863196 MeRIP-seq:(Medium) rs1468673164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527095,Human_RBP_ID_18998363,Human_RBP_ID_22719259 Human_miRNA_ID_1967508 RMVar_hsa_circ_103835,RMVar_hsa_circ_267357,RMVar_hsa_circ_195696 70070 RMVar_ID_70070 Human_SNP_ID_668058912 m1A Human chr19 - 48497638 48497629 48497638 AAAGGCCGGATGGGTAGACAACACGAGGCCGCAGCCACCGCCGCCACCGCTGCCACCGCCACCGG AAAGGCCGGATGGGTAGACAACACGAGGCCGC_________CGCCACCGCTGCCACCGCCACCGG GGCGGTGGCT G LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48497334..48497829 26863196 MeRIP-seq:(Medium) rs767926560 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_5146024 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70071 RMVar_ID_70071 Human_SNP_ID_668058917 m1A Human chr19 - 48497638 48497638 48497638 AAAGGCCGGATGGGTAGACAACACGAGGCCGCAGCCACCGCCGCCACCGCTGCCACCGCCACCGG AAAGGCCGGATGGGTAGACAACACGAGGCCGCGGCCACCGCCGCCACCGCTGCCACCGCCACCGG T C LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48497334..48497829 26863196 MeRIP-seq:(Medium) rs972769621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146024 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70072 RMVar_ID_70072 Human_SNP_ID_668058918 m1A Human chr19 - 48497638 48497638 48497638 AAAGGCCGGATGGGTAGACAACACGAGGCCGCAGCCACCGCCGCCACCGCTGCCACCGCCACCGG AAAGGCCGGATGGGTAGACAACACGAGGCCGCCGCCACCGCCGCCACCGCTGCCACCGCCACCGG T G LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48497334..48497829 26863196 MeRIP-seq:(Medium) rs972769621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146024 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70073 RMVar_ID_70073 Human_SNP_ID_668058966 m1A Human chr19 + 48497784 48497783 48497785 CTCCCAGCCCCTGGGGCTCTCGGCGCCCCCCCAGTCTCGGGGGCTCTCCTCTCGGTCCCGGGTTC CTCCCAGCCCCTGGGGCTCTCGGCGCCCCCCC__TCTCGGGGGCTCTCCTCTCGGTCCCGGGTTC CAG C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:48497679..48497806 26863196 MeRIP-seq:(Medium) rs1555901159 Functional Loss DEL dbSNP153 33..34 33 - - - 70074 RMVar_ID_70074 Human_SNP_ID_668059131 m1A Human chr19 - 48498167 48498167 48498167 AAGTGCTGGAGAATGGGGAGCTGACACCCCCAAGGAGGGAGGAGAAAGCGCTGGAGAATGGGGAG AAGTGCTGGAGAATGGGGAGCTGACACCCCCAGGGAGGGAGGAGAAAGCGCTGGAGAATGGGGAG T C LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48497975..48498493 26863196 MeRIP-seq:(Medium) rs866613109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240398,Human_RBP_ID_909713,Human_RBP_ID_8233509,Human_RBP_ID_21892815 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70075 RMVar_ID_70075 Human_SNP_ID_668059143 m1A Human chr19 - 48498202 48498200 48498203 GAATGGGGCCCTGGGGTCCCCCGAGAGAGAAGAGAAAGTGCTGGAGAATGGGGAGCTGACACCCC GAATGGGGCCCTGGGGTCCCCCGAGAGAGAA___AAAGTGCTGGAGAATGGGGAGCTGACACCCC TCTC T LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48498153..48498326 26863196 MeRIP-seq:(Medium) rs1408362010 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18179768 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70076 RMVar_ID_70076 Human_SNP_ID_668059589 m1A Human chr19 - 48499119 48499119 48499119 GAAGAAGAGGAGGAGGAGGAGGGCAGCTCCCCAGGGGAAGACAGCAGCAGCCTTGGAGGTGGCCC GAAGAAGAGGAGGAGGAGGAGGGCAGCTCCCCGGGGGAAGACAGCAGCAGCCTTGGAGGTGGCCC T C LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48498814..48499162 26863196 MeRIP-seq:(Medium) rs747732618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131402,Human_RBP_ID_9329105,Human_RBP_ID_18461351,Human_RBP_ID_22719262,Human_RBP_ID_26338082 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 70077 RMVar_ID_70077 Human_SNP_ID_668085682 m1A Human chr19 + 48589103 48589103 48589103 GCGGTCAGATGGGGACCGACTGTCGAGAGAGCAGAAGCCGGGAAGCCCGAGAGGCGGCGCTGGCC GCGGTCAGATGGGGACCGACTGTCGAGAGAGCCGAAGCCGGGAAGCCCGAGAGGCGGCGCTGGCC A C SULT2B1 Ensembl:ENSG00000088002 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48589099..48589198 26863196 MeRIP-seq:(Medium) rs909102594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28172 70078 RMVar_ID_70078 Human_SNP_ID_668085693 m1A Human chr19 - 48589140 48589140 48589140 CACCCTAGTCCAGCCACCGTCCCCTCCCCTGGACCCCGGCCAGCGCCGCCTCTCGGGCTTCCCGG CACCCTAGTCCAGCCACCGTCCCCTCCCCTGGCCCCCGGCCAGCGCCGCCTCTCGGGCTTCCCGG T G AC008403.3 Ensembl:ENSG00000287603 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48589097..48589235 26863196 MeRIP-seq:(Medium) rs1057486337 Functional Loss SNV dbSNP153 33..33 33 - - - 70079 RMVar_ID_70079 Human_SNP_ID_668085695 m1A Human chr19 + 48589148 48589148 48589148 CCCGAGAGGCGGCGCTGGCCGGGGTCCAGGGGAGGGGACGGTGGCTGGACTAGGGTGATGGTCAC CCCGAGAGGCGGCGCTGGCCGGGGTCCAGGGGTGGGGACGGTGGCTGGACTAGGGTGATGGTCAC A T SULT2B1 Ensembl:ENSG00000088002 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48589098..48589246 26863196 MeRIP-seq:(Medium) rs1417409018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28172 70080 RMVar_ID_70080 Human_SNP_ID_668085706 m1A Human chr19 - 48589190 48589190 48589190 TCTGTCAGCAAATCCTCCCGGTCTCACCTTCAAAATACCTCCGTGACCATCACCCTAGTCCAGCC TCTGTCAGCAAATCCTCCCGGTCTCACCTTCAGAATACCTCCGTGACCATCACCCTAGTCCAGCC T C AC008403.3 Ensembl:ENSG00000287603 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:48589122..48589204 26863410 MeRIP-seq:(Medium) rs1400959851 Functional Loss SNV dbSNP153 33..33 33 - - - 70081 RMVar_ID_70081 Human_SNP_ID_668094415 m1A Human chr19 - 48615399 48615399 48615399 AAGGGCCGGAAGTTCGAGCGTGCCAGAGGCCGACGGGCCAGCCGAGGCTACAAAAACTAACCCTG AAGGGCCGGAAGTTCGAGCGTGCCAGAGGCCGGCGGGCCAGCCGAGGCTACAAAAACTAACCCTG T C RPL18 Ensembl:ENSG00000063177 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:48615351..48615400 26863196 MeRIP-seq:(Medium) rs151024665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239066,Human_RBP_ID_524928,Human_RBP_ID_769875,Human_RBP_ID_824006,Human_RBP_ID_912546,Human_RBP_ID_1569359,Human_RBP_ID_4571513,Human_RBP_ID_8836143,Human_RBP_ID_17385104,Human_RBP_ID_17656276,Human_RBP_ID_18192370,Human_RBP_ID_18737094,Human_RBP_ID_22533188,Human_RBP_ID_26469546,Human_RBP_ID_26993113,Human_RBP_ID_27157739,Human_RBP_ID_27276728 Human_Splice_Rec_2026964,Human_Splice_Rec_2026972,Human_Splice_Rec_2026974,Human_Splice_Rec_2026984,Human_Splice_Rec_2026994,Human_Splice_Rec_2027006,Human_Splice_Rec_2027016,Human_Splice_Rec_2027032,Human_Splice_Rec_2027044,Human_Splice_Rec_2027066 RMVar_hsa_circ_195699,RMVar_hsa_circ_96970,RMVar_hsa_circ_113169,RMVar_hsa_circ_115545,RMVar_hsa_circ_112247,RMVar_hsa_circ_79282,RMVar_hsa_circ_89776,RMVar_hsa_circ_195701,RMVar_hsa_circ_195702,RMVar_hsa_circ_195703,RMVar_hsa_circ_195700,RMVar_hsa_circ_195698 70082 RMVar_ID_70082 Human_SNP_ID_668094420 m1A Human chr19 + 48615411 48615411 48615411 TTGTAGCCTCGGCTGGCCCGTCGGCCTCTGGCACGCTCGAACTTCCGGCCCTTGGAGCGGACGTA TTGTAGCCTCGGCTGGCCCGTCGGCCTCTGGCGCGCTCGAACTTCCGGCCCTTGGAGCGGACGTA A G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48615363..48615501 26863196 MeRIP-seq:(Medium) rs751090493 Functional Loss SNV dbSNP153 33..33 33 - - - 70083 RMVar_ID_70083 Human_SNP_ID_668094721 m1A Human chr19 - 48616169 48616169 48616169 TATGTGCACTGCGCGTGACCAGCCGGGCCCGCAGCCGCATCCTCAGGGCAGGGGGCAAGATCCTC TATGTGCACTGCGCGTGACCAGCCGGGCCCGCGGCCGCATCCTCAGGGCAGGGGGCAAGATCCTC T C RPL18 Ensembl:ENSG00000063177 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr19:48615965..48616251;chr19:48616120..48616237 26863196 MeRIP-seq:(Medium) rs769334709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239068,Human_RBP_ID_524936,Human_RBP_ID_769878,Human_RBP_ID_824008,Human_RBP_ID_912549,Human_RBP_ID_4571523,Human_RBP_ID_5145355,Human_RBP_ID_8491600,Human_RBP_ID_8836149,Human_RBP_ID_9089142,Human_RBP_ID_17270190,Human_RBP_ID_17696165,Human_RBP_ID_17935038,Human_RBP_ID_18192375,Human_RBP_ID_22447921,Human_RBP_ID_22533450,Human_RBP_ID_22764214,Human_RBP_ID_23131596,Human_RBP_ID_23211332,Human_RBP_ID_26816105 Human_Splice_Rec_2026961,Human_Splice_Rec_2026980,Human_Splice_Rec_2026981,Human_Splice_Rec_2027002,Human_Splice_Rec_2027003,Human_Splice_Rec_2027012,Human_Splice_Rec_2027013,Human_Splice_Rec_2027021,Human_Splice_Rec_2027028,Human_Splice_Rec_2027029,Human_Splice_Rec_2027040,Human_Splice_Rec_2027041,Human_Splice_Rec_2027052,Human_Splice_Rec_2027053,Human_Splice_Rec_2027062,Human_Splice_Rec_2027063 Human_miRNA_ID_1973892,Human_miRNA_ID_1976070,Human_miRNA_ID_2467588,Human_miRNA_ID_2613861,Human_miRNA_ID_3091314 RMVar_hsa_circ_195699,RMVar_hsa_circ_113169,RMVar_hsa_circ_115545,RMVar_hsa_circ_79282,RMVar_hsa_circ_89776,RMVar_hsa_circ_195701,RMVar_hsa_circ_195700,RMVar_hsa_circ_39397,RMVar_hsa_circ_54771,RMVar_hsa_circ_195698,RMVar_hsa_circ_309221,RMVar_hsa_circ_128150,RMVar_hsa_circ_195704,RMVar_hsa_circ_195705 70084 RMVar_ID_70084 Human_SNP_ID_668094992 m1A Human chr19 + 48616775 48616775 48616775 CCTGAACCCGCACATCATCAGTTATGGTCCCCACAACCACGGCCGTCTTGTTTTCCCGGCCAGGA CCTGAACCCGCACATCATCAGTTATGGTCCCCGCAACCACGGCCGTCTTGTTTTCCCGGCCAGGA A G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr19:48616674..48616841;chr19:48616672..48616867;chr19:48616614..48616800 26863196,32194978 MeRIP-seq:(Medium) rs201384708 Functional Loss SNV dbSNP153 33..33 33 - - - 70085 RMVar_ID_70085 Human_SNP_ID_668095461 m1A Human chr19 - 48617814 48617814 48617814 AGGTTCGGCGCAAGGAGCCCAAGAGCCAGGATATCTACCTGAGGCTGTTGGTCAAGGTGAGGCTG AGGTTCGGCGCAAGGAGCCCAAGAGCCAGGATGTCTACCTGAGGCTGTTGGTCAAGGTGAGGCTG T C RPL18 Ensembl:ENSG00000063177 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:48617801..48617900 26863410 MeRIP-seq:(Medium) rs561664573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955344,Human_RBP_ID_4558635,Human_RBP_ID_17386960,Human_RBP_ID_17656290,Human_RBP_ID_19090600,Human_RBP_ID_26816114 Human_Splice_Rec_2026958,Human_Splice_Rec_2026959,Human_Splice_Rec_2026966,Human_Splice_Rec_2026967,Human_Splice_Rec_2026975,Human_Splice_Rec_2026986,Human_Splice_Rec_2026987,Human_Splice_Rec_2026996,Human_Splice_Rec_2026997,Human_Splice_Rec_2027018,Human_Splice_Rec_2027019,Human_Splice_Rec_2027023,Human_Splice_Rec_2027034,Human_Splice_Rec_2027035,Human_Splice_Rec_2027046,Human_Splice_Rec_2027047,Human_Splice_Rec_2027056,Human_Splice_Rec_2027057,Human_Splice_Rec_2027068,Human_Splice_Rec_2027069,Human_Splice_Rec_2027078 RMVar_hsa_circ_195699,RMVar_hsa_circ_79282,RMVar_hsa_circ_89776,RMVar_hsa_circ_39397,RMVar_hsa_circ_54771,RMVar_hsa_circ_195698,RMVar_hsa_circ_128150,RMVar_hsa_circ_344171,RMVar_hsa_circ_195705 70086 RMVar_ID_70086 Human_SNP_ID_668096055 m1A Human chr19 + 48619309 48619309 48619309 TGTGGTGAGTTGGACGACTGACTAGCCGGGCGATAACGGCAGAGAGCATAGAGCGCAGGAACAAG TGTGGTGAGTTGGACGACTGACTAGCCGGGCGGTAACGGCAGAGAGCATAGAGCGCAGGAACAAG A G SPHK2 Ensembl:ENSG00000063176 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48619265..48619488 26863196 MeRIP-seq:(Medium) rs902203464 Functional Loss SNV dbSNP153 33..33 33 - - - 70087 RMVar_ID_70087 Human_SNP_ID_668096109 m1A Human chr19 + 48619459 48619459 48619459 AGGGATCTGGGAGCGAGATGCGTGTAGCTAGCACGATGCGTCGCGCGGTGACGCTCTGGCCCGAC AGGGATCTGGGAGCGAGATGCGTGTAGCTAGCCCGATGCGTCGCGCGGTGACGCTCTGGCCCGAC A C SPHK2 Ensembl:ENSG00000063176 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48619293..48619617 26863196 MeRIP-seq:(Medium) rs1232469075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027089,Human_Splice_Rec_2027099,Human_Splice_Rec_2027109,Human_Splice_Rec_2027121 70088 RMVar_ID_70088 Human_SNP_ID_668097525 m1A Human chr19 - 48624389 48624389 48624389 CCTCCTCCAGGCGGTCCCGCAAGTCAGCACCAACAGCCCCCATCAGACCTAGGGGTGGGGGGAGG CCTCCTCCAGGCGGTCCCGCAAGTCAGCACCAGCAGCCCCCATCAGACCTAGGGGTGGGGGGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48624382..48624627 26863196 MeRIP-seq:(Medium) rs781579222 Functional Loss SNV dbSNP153 33..33 33 - - - 70089 RMVar_ID_70089 Human_SNP_ID_668097658 m1A Human chr19 - 48624898 48624898 48624898 CCAGTCCTGCCCCTCACATTCCCCAGGCCCAGAGCGCCAGGACAGCCCCCCACCCCCCACCGCCT CCAGTCCTGCCCCTCACATTCCCCAGGCCCAGGGCGCCAGGACAGCCCCCCACCCCCCACCGCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48624894..48625026 26863196 MeRIP-seq:(Medium) rs537064466 Functional Loss SNV dbSNP153 33..33 33 - - - 70090 RMVar_ID_70090 Human_SNP_ID_668097661 m1A Human chr19 - 48624906 48624906 48624906 GCCACCTGCCAGTCCTGCCCCTCACATTCCCCAGGCCCAGAGCGCCAGGACAGCCCCCCACCCCC GCCACCTGCCAGTCCTGCCCCTCACATTCCCCCGGCCCAGAGCGCCAGGACAGCCCCCCACCCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48624882..48625023 26863196 MeRIP-seq:(Medium) rs1355985610 Functional Loss SNV dbSNP153 33..33 33 - - - 70091 RMVar_ID_70091 Human_SNP_ID_668099202 m1A Human chr19 + 48629248 48629248 48629248 CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCAGCTCTACACTCACCCGTCTCCGAAGGGGCCCC CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCCGCTCTACACTCACCCGTCTCCGAAGGGGCCCC A C SPHK2 Ensembl:ENSG00000063176 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48629199..48629349 26863196 MeRIP-seq:(Medium) rs747894513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27470099 70092 RMVar_ID_70092 Human_SNP_ID_668099204 m1A Human chr19 - 48629251 48629251 48629251 ACGGGGGCCCCTTCGGAGACGGGTGAGTGTAGAGCTGCCTTGGGAGAGCCAGGAGGTGAAGACAG ACGGGGGCCCCTTCGGAGACGGGTGAGTGTAGCGCTGCCTTGGGAGAGCCAGGAGGTGAAGACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48629201..48629353 26863196 MeRIP-seq:(Medium) rs777587266 Functional Loss SNV dbSNP153 33..33 33 - - - 70093 RMVar_ID_70093 Human_SNP_ID_668099497 m1A Human chr19 + 48629766 48629766 48629766 GCTCACTGGGCCTCCTGGCTGCCCGGGGCGGGAGCCCTGAAACTAAACAAGCTTGGTACCCGCCG GCTCACTGGGCCTCCTGGCTGCCCGGGGCGGGTGCCCTGAAACTAAACAAGCTTGGTACCCGCCG A T SPHK2 Ensembl:ENSG00000063176 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48629717..48629815 26863196 MeRIP-seq:(Medium) rs1435750256 Functional Loss SNV dbSNP153 33..33 33 - - - 70094 RMVar_ID_70094 Human_SNP_ID_668100009 m1A Human chr19 - 48631046 48631046 48631046 AGTGCTCTCCCCCTCTTCTCCTGCAGGATGAGAAATACTGGAGCCGGCGGTACAAGAACAACGAG AGTGCTCTCCCCCTCTTCTCCTGCAGGATGAGGAATACTGGAGCCGGCGGTACAAGAACAACGAG T C DBP Ensembl:ENSG00000105516 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48630896..48631082 26863196 MeRIP-seq:(Medium) rs772223066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027194,Human_Splice_Rec_2027198,Human_Splice_Rec_2027204 70095 RMVar_ID_70095 Human_SNP_ID_668101325 m1A Human chr19 - 48635550 48635550 48635550 CAGGTGCGGCGAAGGGGGCGGGGCGGGTCCTGACGGGGCGGGGCTTGGACTCAGGGGGCGGGGCT CAGGTGCGGCGAAGGGGGCGGGGCGGGTCCTGGCGGGGCGGGGCTTGGACTCAGGGGGCGGGGCT T C DBP Ensembl:ENSG00000105516 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48635545..48635949 26863196 MeRIP-seq:(Medium) rs1352077776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104806,RMVar_hsa_circ_195707,RMVar_hsa_circ_94394,RMVar_hsa_circ_195708 70096 RMVar_ID_70096 Human_SNP_ID_668101369 m1A Human chr19 + 48635640 48635640 48635640 GGCAGCCCGGGCGGGGGCGTGCCCAGGAGAGGAGCGGGGGGAAGCCGAGCCGCACGAACCCGGCC GGCAGCCCGGGCGGGGGCGTGCCCAGGAGAGGCGCGGGGGGAAGCCGAGCCGCACGAACCCGGCC A C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:48635601..48635675 26863196 MeRIP-seq:(Medium) rs1464698386 Functional Loss SNV dbSNP153 33..33 33 - - - 70097 RMVar_ID_70097 Human_SNP_ID_668101815 m1A Human chr19 + 48636959 48636959 48636959 GGGGGTGTCCCGGCCGGGCCGCCCAGCAGCAGAGGGGCCGGGGTCCTGTCGCTCACAGGCCGCGC GGGGGTGTCCCGGCCGGGCCGCCCAGCAGCAGTGGGGCCGGGGTCCTGTCGCTCACAGGCCGCGC A T RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48636912..48637002 26863196 MeRIP-seq:(Medium) rs1298766002 Functional Loss SNV dbSNP153 33..33 33 - - - 70098 RMVar_ID_70098 Human_SNP_ID_668101902 m1A Human chr19 - 48637259 48637259 48637259 AGCGCCTTGAGTCCCCTCTCACCCTCGGTTGCAAAGAGCCGACCGCTTGATCTGGACACCCCCTC AGCGCCTTGAGTCCCCTCTCACCCTCGGTTGCTAAGAGCCGACCGCTTGATCTGGACACCCCCTC T A DBP Ensembl:ENSG00000105516 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48637210..48637321 26863196 MeRIP-seq:(Medium) rs866586525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913562,Human_RBP_ID_4540993,Human_RBP_ID_23803859 Human_miRNA_ID_2646016 RMVar_hsa_circ_94394,RMVar_hsa_circ_195708 70099 RMVar_ID_70099 Human_SNP_ID_668101903 m1A Human chr19 - 48637259 48637259 48637259 AGCGCCTTGAGTCCCCTCTCACCCTCGGTTGCAAAGAGCCGACCGCTTGATCTGGACACCCCCTC AGCGCCTTGAGTCCCCTCTCACCCTCGGTTGCGAAGAGCCGACCGCTTGATCTGGACACCCCCTC T C DBP Ensembl:ENSG00000105516 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48637210..48637321 26863196 MeRIP-seq:(Medium) rs866586525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913562,Human_RBP_ID_4540993,Human_RBP_ID_23803859 Human_miRNA_ID_2646016 RMVar_hsa_circ_94394,RMVar_hsa_circ_195708 70100 RMVar_ID_70100 Human_SNP_ID_668102212 m1A Human chr19 + 48638121 48638121 48638121 ACGGGCGGGTGCAATCCTCGAAGGGGAGTCTCAGCGACCATGGGGGACACCATCCACTGTAAGAC ACGGGCGGGTGCAATCCTCGAAGGGGAGTCTCGGCGACCATGGGGGACACCATCCACTGTAAGAC A G SEC1P Ensembl:ENSG00000232871 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48638072..48638164 26863196 MeRIP-seq:(Medium) rs1330031263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027235,Human_Splice_Rec_2027241,Human_Splice_Rec_2027243 70101 RMVar_ID_70101 Human_SNP_ID_668102217 m1A Human chr19 - 48638129 48638129 48638129 TGTTCTCTGTCTTACAGTGGATGGTGTCCCCCATGGTCGCTGAGACTCCCCTTCGAGGATTGCAC TGTTCTCTGTCTTACAGTGGATGGTGTCCCCCCTGGTCGCTGAGACTCCCCTTCGAGGATTGCAC T G CA11 Ensembl:ENSG00000063180 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48638078..48638281 26863196 MeRIP-seq:(Medium) rs1323916809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4541005,Human_RBP_ID_5117032,Human_RBP_ID_8491639,Human_RBP_ID_22742543 Human_Splice_Rec_2027224,Human_Splice_Rec_2027226,Human_Splice_Rec_2027228,Human_Splice_Rec_2027234 70102 RMVar_ID_70102 Human_SNP_ID_668102607 m1A Human chr19 - 48639028 48639028 48639028 ACTGCAGATGCACTCCCTGAGACTCCTGAGCCAGAATCCTCCATCTCAGATCTTCCAGAGCCTCA ACTGCAGATGCACTCCCTGAGACTCCTGAGCCTGAATCCTCCATCTCAGATCTTCCAGAGCCTCA T A CA11 Ensembl:ENSG00000063180 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48638977..48639070 26863196 MeRIP-seq:(Medium) rs1489455962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027222,Human_Splice_Rec_2027230 70103 RMVar_ID_70103 Human_SNP_ID_668102776 m1A Human chr19 + 48639534 48639534 48639534 GAACCCCCTCGTGTGTGACCACTGCCCCCAGCACGCCAGGGACTTACTCTTGTAGGAGATGCGAG GAACCCCCTCGTGTGTGACCACTGCCCCCAGCCCGCCAGGGACTTACTCTTGTAGGAGATGCGAG A C SEC1P Ensembl:ENSG00000232871 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48639533..48639619 26863196 MeRIP-seq:(Medium) rs141672508 Functional Loss SNV dbSNP153 33..33 33 - - - 70104 RMVar_ID_70104 Human_SNP_ID_668102777 m1A Human chr19 + 48639534 48639534 48639534 GAACCCCCTCGTGTGTGACCACTGCCCCCAGCACGCCAGGGACTTACTCTTGTAGGAGATGCGAG GAACCCCCTCGTGTGTGACCACTGCCCCCAGCTCGCCAGGGACTTACTCTTGTAGGAGATGCGAG A T SEC1P Ensembl:ENSG00000232871 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48639533..48639619 26863196 MeRIP-seq:(Medium) rs141672508 Functional Loss SNV dbSNP153 33..33 33 - - - 70105 RMVar_ID_70105 Human_SNP_ID_668104126 m1A Human chr19 + 48644597 48644597 48644597 AGGCCCTGGGGGTGGGGTCGGAGTAGGAGGACAAGGAGTCAGAAATAGAGACTGGATCCCAGGGC AGGCCCTGGGGGTGGGGTCGGAGTAGGAGGACCAGGAGTCAGAAATAGAGACTGGATCCCAGGGC A C SEC1P Ensembl:ENSG00000232871 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48644595..48644698 26863196 MeRIP-seq:(Medium) rs764327914 Functional Loss SNV dbSNP153 33..33 33 - - - 70106 RMVar_ID_70106 Human_SNP_ID_668110920 m1A Human chr19 + 48668994 48668950 48668995 CTATCACCACCATCATCACCACTATCACCATCACCATCATCACCACTATCACCACCATCATCACC __________________________________CATCATCACCACTATCACCACCATCATCACC TCATCATCACCACTATCACCACCATCATCACCACTATCACCATCAC T SEC1P Ensembl:ENSG00000232871 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48668967..48669148 26863196 MeRIP-seq:(Medium) rs1302546808 Functional Loss DEL dbSNP153 1..34 33 - - - 70107 RMVar_ID_70107 Human_SNP_ID_668110946 m1A Human chr19 + 48668994 48668994 48668994 CTATCACCACCATCATCACCACTATCACCATCACCATCATCACCACTATCACCACCATCATCACC CTATCACCACCATCATCACCACTATCACCATCGCCATCATCACCACTATCACCACCATCATCACC A G SEC1P Ensembl:ENSG00000232871 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48668967..48669148 26863196 MeRIP-seq:(Medium) rs887220466 Functional Loss SNV dbSNP153 33..33 33 - - - 70108 RMVar_ID_70108 Human_SNP_ID_668111709 m1A Human chr19 - 48669885 48669867 48669885 TGGTGGTGGTGGTGATGGTGGTGGTGATGGTGATGGTAGTGGTGATGATGGTGATGGTGGTGGTG TGGTGGTGGTGGTGATGGTGGTGGTGATGGTG__________________GTGATGGTGGTGGTG CCATCATCACCACTACCAT C NTN5 Ensembl:ENSG00000142233 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48669875..48669940 26863196 MeRIP-seq:(Medium) rs1307529312 Functional Loss DEL dbSNP153 33..50 33 - - - 70109 RMVar_ID_70109 Human_SNP_ID_668111723 m1A Human chr19 - 48669885 48669885 48669885 TGGTGGTGGTGGTGATGGTGGTGGTGATGGTGATGGTAGTGGTGATGATGGTGATGGTGGTGGTG TGGTGGTGGTGGTGATGGTGGTGGTGATGGTGGTGGTAGTGGTGATGATGGTGATGGTGGTGGTG T C NTN5 Ensembl:ENSG00000142233 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48669875..48669940 26863196 MeRIP-seq:(Medium) rs1413949538 Functional Loss SNV dbSNP153 33..33 33 - - - 70110 RMVar_ID_70110 Human_SNP_ID_668126393 m1A Human chr19 + 48720701 48720701 48720701 AAACTCAATCTCCCAACATTCCACGCGGGATAAGAACTACAACTCCCAGAAAGCTTTGCGCTCAG AAACTCAATCTCCCAACATTCCACGCGGGATACGAACTACAACTCCCAGAAAGCTTTGCGCTCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48720650..48721026 26863196 MeRIP-seq:(Medium) rs916657406 Functional Loss SNV dbSNP153 33..33 33 - - - 70111 RMVar_ID_70111 Human_SNP_ID_668126394 m1A Human chr19 + 48720701 48720701 48720701 AAACTCAATCTCCCAACATTCCACGCGGGATAAGAACTACAACTCCCAGAAAGCTTTGCGCTCAG AAACTCAATCTCCCAACATTCCACGCGGGATAGGAACTACAACTCCCAGAAAGCTTTGCGCTCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48720650..48721026 26863196 MeRIP-seq:(Medium) rs916657406 Functional Loss SNV dbSNP153 33..33 33 - - - 70112 RMVar_ID_70112 Human_SNP_ID_668128128 m1A Human chr19 - 48727032 48727032 48727032 CTGCTTAGCTTTGTGCAGGAGAAGGTGCTGGAAATGGAGAAGGAGGCTGACCAAGAGGGTGAGCT CTGCTTAGCTTTGTGCAGGAGAAGGTGCTGGAGATGGAGAAGGAGGCTGACCAAGAGGGTGAGCT T C RASIP1 Ensembl:ENSG00000105538 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48727017..48727107 26863196 MeRIP-seq:(Medium) rs1049498878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027359 RMVar_hsa_circ_9617,RMVar_hsa_circ_265410,RMVar_hsa_circ_12269 70113 RMVar_ID_70113 Human_SNP_ID_668128785 m1A Human chr19 + 48729294 48729293 48729294 AGCCACGGCGGCCTCGCAGGCCCCGAGCCCCCAGTGCGGGGGTCCTTGTACATGAACAGGAAGTG AGCCACGGCGGCCTCGCAGGCCCCGAGCCCCC_GTGCGGGGGTCCTTGTACATGAACAGGAAGTG CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48729248..48729422 26863196 MeRIP-seq:(Medium) rs770876421 Functional Loss DEL dbSNP153 33..33 33 - - - 70114 RMVar_ID_70114 Human_SNP_ID_668128787 m1A Human chr19 + 48729294 48729294 48729294 AGCCACGGCGGCCTCGCAGGCCCCGAGCCCCCAGTGCGGGGGTCCTTGTACATGAACAGGAAGTG AGCCACGGCGGCCTCGCAGGCCCCGAGCCCCCGGTGCGGGGGTCCTTGTACATGAACAGGAAGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48729248..48729422 26863196 MeRIP-seq:(Medium) rs1190929544 Functional Loss SNV dbSNP153 33..33 33 - - - 70115 RMVar_ID_70115 Human_SNP_ID_668131691 m1A Human chr19 - 48739629 48739629 48739629 CCCGGCGGACTCCCAGGTCTTCTTCGTCGGACACGGGGAGCCGCAGCAGCGAGCCGCTACCTCCG CCCGGCGGACTCCCAGGTCTTCTTCGTCGGACTCGGGGAGCCGCAGCAGCGAGCCGCTACCTCCG T A RASIP1 Ensembl:ENSG00000105538 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48739626..48739739 26863196 MeRIP-seq:(Medium) rs969701099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027350 70116 RMVar_ID_70116 Human_SNP_ID_668131692 m1A Human chr19 - 48739629 48739629 48739629 CCCGGCGGACTCCCAGGTCTTCTTCGTCGGACACGGGGAGCCGCAGCAGCGAGCCGCTACCTCCG CCCGGCGGACTCCCAGGTCTTCTTCGTCGGACGCGGGGAGCCGCAGCAGCGAGCCGCTACCTCCG T C RASIP1 Ensembl:ENSG00000105538 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48739626..48739739 26863196 MeRIP-seq:(Medium) rs969701099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027350 70117 RMVar_ID_70117 Human_SNP_ID_668131751 m1A Human chr19 + 48739825 48739822 48739826 TGGGGACAGACGCGAGGCAAAGAGAGAGAGAAAAAATAAATAAATAAAGGCAAGTCCCACAGTAG TGGGGACAGACGCGAGGCAAAGAGAGAGAG____AATAAATAAATAAAGGCAAGTCCCACAGTAG GAAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48739821..48739979 26863196 MeRIP-seq:(Medium) rs1279030083 Functional Loss DEL dbSNP153 31..34 33 - - - 70118 RMVar_ID_70118 Human_SNP_ID_668136285 m1A Human chr19 + 48754919 48754884 48754920 ACCCAGACCCTTCTGCTCACACCCAGCAGTCCAGGCCCCCAGACCCTCCTCCCTCAGACTTAGGA __________________________________GCCCCCAGACCCTCCTCCCTCAGACTTAGGA AGCACCCAGACCCTTCTGCTCACACCCAGCAGTCCAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48754914..48755046 26863196 MeRIP-seq:(Medium) rs1390034012 Functional Loss DEL dbSNP153 1..34 33 - - - 70119 RMVar_ID_70119 Human_SNP_ID_668136936 m1A Human chr19 + 48756651 48756651 48756651 GGGCTGGGGATCTGGGCCCCTGGGTCTGAGGGAGGAGGGGCTGGGTCTGGACCCCTGGGTCTGAG GGGCTGGGGATCTGGGCCCCTGGGTCTGAGGGGGGAGGGGCTGGGTCTGGACCCCTGGGTCTGAG A G FGF21 Ensembl:ENSG00000105550 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48756637..48756754 26863196 MeRIP-seq:(Medium) rs1420938044 Functional Loss SNV dbSNP153 33..33 33 - - - 70120 RMVar_ID_70120 Human_SNP_ID_668148420 m1A Human chr19 - 48795349 48795349 48795349 CACGCCAGCACTCGCCTCCCTACCAATGACTCACCTGAAGTGCAATACGAAATAAAAGGCCAGCG CACGCCAGCACTCGCCTCCCTACCAATGACTCCCCTGAAGTGCAATACGAAATAAAAGGCCAGCG T G BCAT2 Ensembl:ENSG00000105552 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48795158..48795409 26863196 MeRIP-seq:(Medium) rs1236704936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569413,Human_RBP_ID_1890787,Human_RBP_ID_17270206,Human_RBP_ID_17387461,Human_RBP_ID_27470131 Human_miRNA_ID_2275740,Human_miRNA_ID_2401634,Human_miRNA_ID_2495560,Human_miRNA_ID_2501482,Human_miRNA_ID_3109510,Human_miRNA_ID_3110958 RMVar_hsa_circ_111797,RMVar_hsa_circ_122731,RMVar_hsa_circ_195720,RMVar_hsa_circ_92237,RMVar_hsa_circ_94812,RMVar_hsa_circ_89848,RMVar_hsa_circ_195721,RMVar_hsa_circ_195718,RMVar_hsa_circ_195719,RMVar_hsa_circ_195717 70121 RMVar_ID_70121 Human_SNP_ID_668148471 m1A Human chr19 - 48795463 48795463 48795463 CACCTCACGCACTGCCTCCGTTGTTCCGCAGTACGGAATCAGAGCCCACGAGTGGATGTTCCCGG CACCTCACGCACTGCCTCCGTTGTTCCGCAGTGCGGAATCAGAGCCCACGAGTGGATGTTCCCGG T C BCAT2 Ensembl:ENSG00000105552 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:48795151..48795475 32194978 MeRIP-seq:(Medium) rs1269472186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4541139 Human_Splice_Rec_2027504,Human_Splice_Rec_2027524,Human_Splice_Rec_2027546,Human_Splice_Rec_2027566,Human_Splice_Rec_2027586 RMVar_hsa_circ_111797,RMVar_hsa_circ_122731,RMVar_hsa_circ_195720,RMVar_hsa_circ_92237,RMVar_hsa_circ_94812,RMVar_hsa_circ_89848,RMVar_hsa_circ_195721,RMVar_hsa_circ_195718,RMVar_hsa_circ_195719,RMVar_hsa_circ_195717 70122 RMVar_ID_70122 Human_SNP_ID_668148788 m1A Human chr19 - 48796468 48796468 48796468 CCTCCACATTCCCACCATGGAAAATGGGCCTGAGCTGATCCTCCGCTTCCAGAAGGAGCTGAAGG CCTCCACATTCCCACCATGGAAAATGGGCCTGGGCTGATCCTCCGCTTCCAGAAGGAGCTGAAGG T C BCAT2 Ensembl:ENSG00000105552 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:48796426..48796525 32194978 MeRIP-seq:(Medium) rs993016942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525013,Human_RBP_ID_13492543,Human_RBP_ID_23803929 Human_Splice_Rec_2027502,Human_Splice_Rec_2027503,Human_Splice_Rec_2027522,Human_Splice_Rec_2027523,Human_Splice_Rec_2027544,Human_Splice_Rec_2027545,Human_Splice_Rec_2027562,Human_Splice_Rec_2027563,Human_Splice_Rec_2027584,Human_Splice_Rec_2027585,Human_Splice_Rec_2027600,Human_Splice_Rec_2027606,Human_Splice_Rec_2027624 RMVar_hsa_circ_111797,RMVar_hsa_circ_122731,RMVar_hsa_circ_195720,RMVar_hsa_circ_92237,RMVar_hsa_circ_94812,RMVar_hsa_circ_89848,RMVar_hsa_circ_195721,RMVar_hsa_circ_195718,RMVar_hsa_circ_195719,RMVar_hsa_circ_195717 70123 RMVar_ID_70123 Human_SNP_ID_668148801 m1A Human chr19 - 48796501 48796501 48796501 GGCTTGGTCCTCACCGCACCTTCTGTCCCAGAACCTCCACATTCCCACCATGGAAAATGGGCCTG GGCTTGGTCCTCACCGCACCTTCTGTCCCAGAGCCTCCACATTCCCACCATGGAAAATGGGCCTG T C BCAT2 Ensembl:ENSG00000105552 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48796451..48796675 32194978 MeRIP-seq:(Medium) rs755170050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5469022,Human_RBP_ID_9089149,Human_RBP_ID_18737154 Human_Splice_Rec_2027502,Human_Splice_Rec_2027503,Human_Splice_Rec_2027522,Human_Splice_Rec_2027523,Human_Splice_Rec_2027544,Human_Splice_Rec_2027545,Human_Splice_Rec_2027562,Human_Splice_Rec_2027563,Human_Splice_Rec_2027584,Human_Splice_Rec_2027585,Human_Splice_Rec_2027600,Human_Splice_Rec_2027606,Human_Splice_Rec_2027624 RMVar_hsa_circ_111797,RMVar_hsa_circ_122731,RMVar_hsa_circ_195720,RMVar_hsa_circ_92237,RMVar_hsa_circ_94812,RMVar_hsa_circ_89848,RMVar_hsa_circ_195721,RMVar_hsa_circ_195718,RMVar_hsa_circ_195719,RMVar_hsa_circ_195717 70124 RMVar_ID_70124 Human_SNP_ID_668149936 m1A Human chr19 - 48799840 48799840 48799840 TGGACTCCTGACGCTGTCCCTTTGCCCGTCGCAGCCCTCGCTGGGTGTCAGCCAGCCCACGCGCG TGGACTCCTGACGCTGTCCCTTTGCCCGTCGCGGCCCTCGCTGGGTGTCAGCCAGCCCACGCGCG T C BCAT2 Ensembl:ENSG00000105552 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:48799810..48800052 32194978 MeRIP-seq:(Medium) rs773653450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10100,RMVar_hsa_circ_94812,RMVar_hsa_circ_195721 70125 RMVar_ID_70125 Human_SNP_ID_668150130 m1A Human chr19 - 48800285 48800285 48800285 CCACCCGCGTGTCCCCGCAGCTGTTTGAGGGCATGAAGGCGTTCAAAGGCAAAGACCAGCAGGTG CCACCCGCGTGTCCCCGCAGCTGTTTGAGGGCCTGAAGGCGTTCAAAGGCAAAGACCAGCAGGTG T G BCAT2 Ensembl:ENSG00000105552 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:48800236..48806704 32194978 MeRIP-seq:(Medium) rs1167805172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569420,Human_RBP_ID_4558640,Human_RBP_ID_20409771 Human_Splice_Rec_2027490,Human_Splice_Rec_2027491,Human_Splice_Rec_2027510,Human_Splice_Rec_2027511,Human_Splice_Rec_2027532,Human_Splice_Rec_2027533,Human_Splice_Rec_2027550,Human_Splice_Rec_2027551,Human_Splice_Rec_2027572,Human_Splice_Rec_2027573,Human_Splice_Rec_2027588,Human_Splice_Rec_2027589,Human_Splice_Rec_2027612,Human_Splice_Rec_2027613,Human_Splice_Rec_2027628,Human_Splice_Rec_2027629,Human_Splice_Rec_2027640,Human_Splice_Rec_2027641 RMVar_hsa_circ_10100,RMVar_hsa_circ_94812,RMVar_hsa_circ_195721,RMVar_hsa_circ_33937,RMVar_hsa_circ_195722 70126 RMVar_ID_70126 Human_SNP_ID_668151584 m1A Human chr19 - 48806131 48806131 48806131 AGAGGTGACAGGGTGATGGTAGGAAAGGGGACAGCCGGGGGGCTGGCGGGAGAGGGACAGCCAGG AGAGGTGACAGGGTGATGGTAGGAAAGGGGACGGCCGGGGGGCTGGCGGGAGAGGGACAGCCAGG T C BCAT2 Ensembl:ENSG00000105552 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48806124..48806238 26863196 MeRIP-seq:(Medium) rs956123237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241390,Human_RBP_ID_264043,Human_RBP_ID_9426337,Human_RBP_ID_17068398 RMVar_hsa_circ_10100,RMVar_hsa_circ_195722 70127 RMVar_ID_70127 Human_SNP_ID_668151756 m1A Human chr19 + 48806670 48806670 48806670 GTCTTCCCAAACACCAGGGGCTCGCCGGGGCCAGGCTTCTTATGAGGCTTCTGTGTCATTTCCAG GTCTTCCCAAACACCAGGGGCTCGCCGGGGCCCGGCTTCTTATGAGGCTTCTGTGTCATTTCCAG A C NONHSAG026188.2 RNACentral:URS00009B9598 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48806463..48806746 26863196 MeRIP-seq:(Medium) rs968654344 Functional Loss SNV dbSNP153 33..33 33 - - - 70128 RMVar_ID_70128 Human_SNP_ID_668151757 m1A Human chr19 + 48806670 48806670 48806670 GTCTTCCCAAACACCAGGGGCTCGCCGGGGCCAGGCTTCTTATGAGGCTTCTGTGTCATTTCCAG GTCTTCCCAAACACCAGGGGCTCGCCGGGGCCGGGCTTCTTATGAGGCTTCTGTGTCATTTCCAG A G NONHSAG026188.2 RNACentral:URS00009B9598 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48806463..48806746 26863196 MeRIP-seq:(Medium) rs968654344 Functional Loss SNV dbSNP153 33..33 33 - - - 70129 RMVar_ID_70129 Human_SNP_ID_668151887 m1A Human chr19 + 48807058 48807058 48807058 TGGGACCACACAGAAGCCAAGGGACAGAGAGAAGCTTTCGTGCCCAGATCTGGGTGGAGAAAGAA TGGGACCACACAGAAGCCAAGGGACAGAGAGAGGCTTTCGTGCCCAGATCTGGGTGGAGAAAGAA A G NONHSAG026188.2 RNACentral:URS00009B9598 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:48799726..48807134;chr19:48806976..48807075 26863196 MeRIP-seq:(Medium) rs748515019 Functional Loss SNV dbSNP153 33..33 33 - - - 70130 RMVar_ID_70130 Human_SNP_ID_668152824 m1A Human chr19 + 48810807 48810807 48810807 CCCACCTCATCCGCGTCTACCTGCTCCCCCTCACCCCATTAAAGCCTCGTGCTCCTTTCCAAAGG CCCACCTCATCCGCGTCTACCTGCTCCCCCTCCCCCCATTAAAGCCTCGTGCTCCTTTCCAAAGG A C NONHSAG026188.2 RNACentral:URS00009B9598 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48810798..48811025 26863196 MeRIP-seq:(Medium) rs1223519619 Functional Loss SNV dbSNP153 33..33 33 - - - 70131 RMVar_ID_70131 Human_SNP_ID_668153285 m1A Human chr19 - 48812167 48812167 48812167 GACAGAGTGTCCCAGGGTAGGATTGCCGAGACACGATGGCCGAGGGATACGATTTTTTTTTTTTT GACAGAGTGTCCCAGGGTAGGATTGCCGAGACCCGATGGCCGAGGGATACGATTTTTTTTTTTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48812164..48812302 26863196 MeRIP-seq:(Medium) rs1261739275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13492866 70132 RMVar_ID_70132 Human_SNP_ID_668161091 m1A Human chr19 + 48837370 48837370 48837370 TCTTGTGGCAGGACCGGAGGGGCGATCCCGGCATCCCACGCGGGCCCCCAGGGGGTGGGACCTCC TCTTGTGGCAGGACCGGAGGGGCGATCCCGGCGTCCCACGCGGGCCCCCAGGGGGTGGGACCTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48837195..48838154 32194978 MeRIP-seq:(Medium) rs1568529571 Functional Loss SNV dbSNP153 33..33 33 - - - 70133 RMVar_ID_70133 Human_SNP_ID_668167717 m1A Human chr19 - 48860444 48860444 48860444 GCCTTCTCTTCCCGCAGGCAGAGCACCCGGGCATGAGGACCTACGTTTTGGCCGCTGACACCTTA GCCTTCTCTTCCCGCAGGCAGAGCACCCGGGCGTGAGGACCTACGTTTTGGCCGCTGACACCTTA T C PLEKHA4 Ensembl:ENSG00000105559 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48860393..48861434 32194978 MeRIP-seq:(Medium) rs1009877027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2027710,Human_Splice_Rec_2027711,Human_Splice_Rec_2027742,Human_Splice_Rec_2027743,Human_Splice_Rec_2027816,Human_Splice_Rec_2027817,Human_Splice_Rec_2027826,Human_Splice_Rec_2027827 RMVar_hsa_circ_48827 70134 RMVar_ID_70134 Human_SNP_ID_668170034 m1A Human chr19 - 48868473 48868473 48868473 GTGTGAAGGAGAGAGGACACAGGGGATGACTGAGAGACAGAGAGAGAGAGAGAGAGAGAATGAGA GTGTGAAGGAGAGAGGACACAGGGGATGACTGGGAGACAGAGAGAGAGAGAGAGAGAGAATGAGA T C PLEKHA4 Ensembl:ENSG00000105559 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:48868469..48868609 26863196 MeRIP-seq:(Medium) rs547076062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23803982,Human_RBP_ID_26474239 70135 RMVar_ID_70135 Human_SNP_ID_668170042 m1A Human chr19 - 48868496 48868496 48868496 AGAGAGAAAGAGGAAGAGACTGAGTGTGAAGGAGAGAGGACACAGGGGATGACTGAGAGACAGAG AGAGAGAAAGAGGAAGAGACTGAGTGTGAAGGGGAGAGGACACAGGGGATGACTGAGAGACAGAG T C PLEKHA4 Ensembl:ENSG00000105559 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:48868377..48868614;chr19:48868088..48868650;chr19:48867583..48868650 26863196 MeRIP-seq:(Medium) rs1299046392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26474239 70136 RMVar_ID_70136 Human_SNP_ID_668171249 m1A Human chr19 - 48872485 48872485 48872485 TATCTCCGGCTGCCTCAAGTGCCGTGGCGACAAGCGGGCGCGGGGTCGTGCAGCGTCTTGCATAA TATCTCCGGCTGCCTCAAGTGCCGTGGCGACAGGCGGGCGCGGGGTCGTGCAGCGTCTTGCATAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48872426..48872676 26863196 MeRIP-seq:(Medium) rs977167296 Functional Loss SNV dbSNP153 33..33 33 - - - 70137 RMVar_ID_70137 Human_SNP_ID_668171742 m1A Human chr19 + 48873951 48873951 48873951 ATCAAGCCACGGAGGATAAAAGAACAGAAAGAAGTAAAGGAGCCAGGAAGACCTCCGTGTCCCCC ATCAAGCCACGGAGGATAAAAGAACAGAAAGATGTAAAGGAGCCAGGAAGACCTCCGTGTCCCCC A T PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48873576..48874810 26863196 MeRIP-seq:(Medium) rs754521332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52796,Human_RBP_ID_1569445,Human_RBP_ID_4541270,Human_RBP_ID_5145358,Human_RBP_ID_8491721,Human_RBP_ID_26338091,Human_RBP_ID_26472782,Human_RBP_ID_27815560 RMVar_hsa_circ_89556,RMVar_hsa_circ_195728 70138 RMVar_ID_70138 Human_SNP_ID_668171965 m1A Human chr19 + 48874426 48874424 48874427 GTCCTGGGTCTATCAGCCAGGAGAGGACACAGAGGAGGAGGAAGATGAGGACAGTGATACAGGAT GTCCTGGGTCTATCAGCCAGGAGAGGACACA___GAGGAGGAAGATGAGGACAGTGATACAGGAT AGAG A PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:48874376..48874450;chr19:48874376..48874910 32194978 MeRIP-seq:(Medium) rs781175895 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_52797,Human_RBP_ID_239292,Human_RBP_ID_525041,Human_RBP_ID_5145847,Human_RBP_ID_6778245,Human_RBP_ID_9259035,Human_RBP_ID_22070416,Human_RBP_ID_24545522,Human_RBP_ID_26472787 RMVar_hsa_circ_89556,RMVar_hsa_circ_195728 70139 RMVar_ID_70139 Human_SNP_ID_668172088 m1A Human chr19 - 48874728 48874709 48874728 CACTCGGAAGGGGCAGGGCTCAGCTTCTCCCCAGTCCTCAGCAGCTTCCTCTTCCTCTGTCTCTT CACTCGGAAGGGGCAGGGCTCAGCTTCTCCCC___________________TTCCTCTGTCTCTT AGAGGAAGCTGCTGAGGACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48874679..48874838 26863196 MeRIP-seq:(Medium) rs755872668 Functional Loss DEL dbSNP153 33..51 33 - - - 70140 RMVar_ID_70140 Human_SNP_ID_668172504 m1A Human chr19 - 48875692 48875692 48875692 GAAGCGGCTGCGATCCCGAGCAAGCTGCTCCCAGGGGCCCTGGCGGGCGGCCTGGGCCGGCCCTG GAAGCGGCTGCGATCCCGAGCAAGCTGCTCCCCGGGGCCCTGGCGGGCGGCCTGGGCCGGCCCTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48875601..48875800 32194978 MeRIP-seq:(Medium) rs571123568 Functional Loss SNV dbSNP153 33..33 33 - - - 70141 RMVar_ID_70141 Human_SNP_ID_668172559 m1A Human chr19 + 48875770 48875770 48875770 CCCAGGCCCAGGAGGAGCTGAGCCCCTGCCTCACCCCTGCTGCCCGGGCCAGAGCCTGGGCACGC CCCAGGCCCAGGAGGAGCTGAGCCCCTGCCTCCCCCCTGCTGCCCGGGCCAGAGCCTGGGCACGC A C PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48875743..48875869 26863196 MeRIP-seq:(Medium) rs759405447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770228,Human_RBP_ID_5117037 RMVar_hsa_circ_89556,RMVar_hsa_circ_99949,RMVar_hsa_circ_195728,RMVar_hsa_circ_195729 70142 RMVar_ID_70142 Human_SNP_ID_668172560 m1A Human chr19 + 48875770 48875770 48875770 CCCAGGCCCAGGAGGAGCTGAGCCCCTGCCTCACCCCTGCTGCCCGGGCCAGAGCCTGGGCACGC CCCAGGCCCAGGAGGAGCTGAGCCCCTGCCTCTCCCCTGCTGCCCGGGCCAGAGCCTGGGCACGC A T PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48875743..48875869 26863196 MeRIP-seq:(Medium) rs759405447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770228,Human_RBP_ID_5117037 RMVar_hsa_circ_89556,RMVar_hsa_circ_99949,RMVar_hsa_circ_195728,RMVar_hsa_circ_195729 70143 RMVar_ID_70143 Human_SNP_ID_668179971 m1A Human chr19 - 48900849 48900849 48900849 GGGGGACAGCCAGCACGGCGCGAAGCAGGAGCAGCAGCAGCAGCGGCAACAGAAGGAGGGTTCCT GGGGGACAGCCAGCACGGCGCGAAGCAGGAGCCGCAGCAGCAGCGGCAACAGAAGGAGGGTTCCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr19:48900776..48900952;chr19:48900776..48900925 26863196 MeRIP-seq:(Medium) rs1348390568 Functional Loss SNV dbSNP153 33..33 33 - - - 70144 RMVar_ID_70144 Human_SNP_ID_668180510 m1A Human chr19 + 48902731 48902729 48902731 TGAGTTCTGAACTGGAGAGATATGTTAAGTCAAGAGCAAGGAAGAGAGGAAGTGAGGGGAAGAGC TGAGTTCTGAACTGGAGAGATATGTTAAGTC__GAGCAAGGAAGAGAGGAAGTGAGGGGAAGAGC CAA C NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48902729..48902810 26863196 MeRIP-seq:(Medium) rs1254317176 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_195733,RMVar_hsa_circ_94007 70145 RMVar_ID_70145 Human_SNP_ID_668181047 m1A Human chr19 + 48904235 48904233 48904235 TTTCATCTTTGCTGCATATGTGGGAAAAGGTAAAAACTGAGTCCCTTGTCAGCTGCCCCAGGGAG TTTCATCTTTGCTGCATATGTGGGAAAAGGT__AAACTGAGTCCCTTGTCAGCTGCCCCAGGGAG TAA T NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48904230..48904450 26863196 MeRIP-seq:(Medium) rs764994272 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3581505,Human_RBP_ID_8197907 RMVar_hsa_circ_195733,RMVar_hsa_circ_94007 70146 RMVar_ID_70146 Human_SNP_ID_668183636 m1A Human chr19 + 48913021 48913021 48913021 ATGACCCTGTGCCTTTCCCCAGGCCACCCGGGACCTTGCCCAGTACGACGCAGCCCATCATGAAG ATGACCCTGTGCCTTTCCCCAGGCCACCCGGGGCCTTGCCCAGTACGACGCAGCCCATCATGAAG A G NUCB1 Ensembl:ENSG00000104805 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48913001..48913075 32194978 MeRIP-seq:(Medium) rs751746542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22763109 Human_Splice_Rec_2027906,Human_Splice_Rec_2027930,Human_Splice_Rec_2027954,Human_Splice_Rec_2027988,Human_Splice_Rec_2027998 RMVar_hsa_circ_195739,RMVar_hsa_circ_195733,RMVar_hsa_circ_94007,RMVar_hsa_circ_373108,RMVar_hsa_circ_195734,RMVar_hsa_circ_363991,RMVar_hsa_circ_195738,RMVar_hsa_circ_77486,RMVar_hsa_circ_195737,RMVar_hsa_circ_305342,RMVar_hsa_circ_371778,RMVar_hsa_circ_195740,RMVar_hsa_circ_195742,RMVar_hsa_circ_115478,RMVar_hsa_circ_287255,RMVar_hsa_circ_195741 70147 RMVar_ID_70147 Human_SNP_ID_668183687 m1A Human chr19 + 48913132 48913132 48913132 TCTGGAGTCACTGGGAGAGGAGCAGAGAAAGGAGGCGGAGAGGAAGCTGGAAGAGCAACAGCGCC TCTGGAGTCACTGGGAGAGGAGCAGAGAAAGGGGGCGGAGAGGAAGCTGGAAGAGCAACAGCGCC A G NUCB1 Ensembl:ENSG00000104805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48912973..48913613 26863196 MeRIP-seq:(Medium) rs1253236460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239435,Human_RBP_ID_770475,Human_RBP_ID_826181,Human_RBP_ID_908839,Human_RBP_ID_5193307,Human_RBP_ID_9381258,Human_RBP_ID_18470738,Human_RBP_ID_22447929,Human_RBP_ID_22764221,Human_RBP_ID_24545529,Human_RBP_ID_26336558 Human_Splice_Rec_2027907,Human_Splice_Rec_2027931,Human_Splice_Rec_2027955,Human_Splice_Rec_2027989,Human_Splice_Rec_2027999 RMVar_hsa_circ_195739,RMVar_hsa_circ_195733,RMVar_hsa_circ_94007,RMVar_hsa_circ_373108,RMVar_hsa_circ_195734,RMVar_hsa_circ_363991,RMVar_hsa_circ_195738,RMVar_hsa_circ_77486,RMVar_hsa_circ_195737,RMVar_hsa_circ_305342,RMVar_hsa_circ_371778,RMVar_hsa_circ_195740,RMVar_hsa_circ_195742,RMVar_hsa_circ_115478,RMVar_hsa_circ_287255,RMVar_hsa_circ_195741 70148 RMVar_ID_70148 Human_SNP_ID_668185321 m1A Human chr19 + 48918783 48918783 48918783 TGAGCAGGAGCTGGAGGCACTCTTCACCAAGGAGGTGAGCATCTTGGAAGCCTCGGGCACCTGGA TGAGCAGGAGCTGGAGGCACTCTTCACCAAGGCGGTGAGCATCTTGGAAGCCTCGGGCACCTGGA A C NUCB1 Ensembl:ENSG00000104805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48918687..48918826 26863196 MeRIP-seq:(Medium) rs1347756146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826182,Human_RBP_ID_5370577,Human_RBP_ID_17935481,Human_RBP_ID_18470635,Human_RBP_ID_18998373,Human_RBP_ID_22594300,Human_RBP_ID_22764225,Human_RBP_ID_26336559 Human_Splice_Rec_2027910,Human_Splice_Rec_2027911,Human_Splice_Rec_2027934,Human_Splice_Rec_2027935,Human_Splice_Rec_2027992,Human_Splice_Rec_2027993,Human_Splice_Rec_2028002,Human_Splice_Rec_2028003,Human_Splice_Rec_2028009 RMVar_hsa_circ_195738,RMVar_hsa_circ_77486,RMVar_hsa_circ_20588,RMVar_hsa_circ_265024,RMVar_hsa_circ_302705 70149 RMVar_ID_70149 Human_SNP_ID_668186094 m1A Human chr19 - 48921114 48921114 48921114 GCAGGCACAGGGGCCATCAGGGGCACAGGTCCAACCTCGGCCCACCCATGTTGGAGAGGGTTGTG GCAGGCACAGGGGCCATCAGGGGCACAGGTCCGACCTCGGCCCACCCATGTTGGAGAGGGTTGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48921112..48921362 26863196 MeRIP-seq:(Medium) rs1424445571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108623,RMVar_hsa_circ_195743 70150 RMVar_ID_70150 Human_SNP_ID_668186560 m1A Human chr19 - 48922454 48922454 48922454 CATCCAGCGCCCATCAGTCGCCTTGGAGCATCAGGAATCCTGAGGGCTGGGGTCCCGGAGGATCA CATCCAGCGCCCATCAGTCGCCTTGGAGCATCGGGAATCCTGAGGGCTGGGGTCCCGGAGGATCA T C lnc-TULP2-4,lnc-TULP2-4:2 RNACentral:URS00008BA484,RNACentral:URS00009C54CE lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48922403..48922818 26863196 MeRIP-seq:(Medium) rs201809235 Functional Loss SNV dbSNP153 33..33 33 - - - 70151 RMVar_ID_70151 Human_SNP_ID_668187050 m1A Human chr19 + 48924205 48924205 48924205 AGGCGGATAGATCACGAGGTCAGGAGATGGAGACCATCCCGGCTAACACGGTGAAACCCTTTCTC AGGCGGATAGATCACGAGGTCAGGAGATGGAGCCCATCCCGGCTAACACGGTGAAACCCTTTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48924091..48924266;chr19:48924116..48924263;chr19:48924085..48924282 26863196 MeRIP-seq:(Medium) rs1177479557 Functional Loss SNV dbSNP153 33..33 33 - - - 70152 RMVar_ID_70152 Human_SNP_ID_668196079 m1A Human chr19 - 48954927 48954927 48954927 CGCCTCTGGGCTGCTCCCCGGACCCGTCCATCACCGCCGCTCCCGCCGCCGCCTCTCGCCGGGTC CGCCTCTGGGCTGCTCCCCGGACCCGTCCATCGCCGCCGCTCCCGCCGCCGCCTCTCGCCGGGTC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:48954876..48955046;chr19:48954826..48955000 26863196,26863410 MeRIP-seq:(Medium) rs1056571866 Functional Loss SNV dbSNP153 33..33 33 - - - 70153 RMVar_ID_70153 Human_SNP_ID_668196080 m1A Human chr19 - 48954927 48954927 48954927 CGCCTCTGGGCTGCTCCCCGGACCCGTCCATCACCGCCGCTCCCGCCGCCGCCTCTCGCCGGGTC CGCCTCTGGGCTGCTCCCCGGACCCGTCCATCCCCGCCGCTCCCGCCGCCGCCTCTCGCCGGGTC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:48954876..48955046;chr19:48954826..48955000 26863196,26863410 MeRIP-seq:(Medium) rs1056571866 Functional Loss SNV dbSNP153 33..33 33 - - - 70154 RMVar_ID_70154 Human_SNP_ID_668196085 m1A Human chr19 - 48954938 48954938 48954938 CGCCTCACCCCCGCCTCTGGGCTGCTCCCCGGACCCGTCCATCACCGCCGCTCCCGCCGCCGCCT CGCCTCACCCCCGCCTCTGGGCTGCTCCCCGGCCCCGTCCATCACCGCCGCTCCCGCCGCCGCCT T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:48954837..48955000 26863410 MeRIP-seq:(Medium) rs894774952 Functional Loss SNV dbSNP153 33..33 33 - - - 70155 RMVar_ID_70155 Human_SNP_ID_668196090 m1A Human chr19 + 48954948 48954948 48954948 GGGAGCGGCGGTGATGGACGGGTCCGGGGAGCAGCCCAGAGGCGGGGGTGAGGCGGGAGGCAGAC GGGAGCGGCGGTGATGGACGGGTCCGGGGAGCGGCCCAGAGGCGGGGGTGAGGCGGGAGGCAGAC A G BAX Ensembl:ENSG00000087088 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48954826..48955038;chr19:48954850..48954975;chr19:48954826..48955202;chr19:48954826..48955074;chr19:48954826..48955068 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1478724845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239301,Human_RBP_ID_770237,Human_RBP_ID_824238,Human_RBP_ID_914216,Human_RBP_ID_4557643,Human_RBP_ID_5117767,Human_RBP_ID_8728085,Human_RBP_ID_19093912 Human_Splice_Rec_2028067,Human_Splice_Rec_2028077,Human_Splice_Rec_2028085,Human_Splice_Rec_2028089,Human_Splice_Rec_2028093,Human_Splice_Rec_2028105,Human_Splice_Rec_2028115,Human_Splice_Rec_2028123,Human_Splice_Rec_2028135 RMVar_hsa_circ_127888,RMVar_hsa_circ_195747 70156 RMVar_ID_70156 Human_SNP_ID_668196269 m1A Human chr19 + 48955505 48955504 48955505 CCGTGAGTCTCCACAGTCTCCTGATCCCCTAGAACCCAAGAGTCCAGGTACCTCTTCCCTTCCTT CCGTGAGTCTCCACAGTCTCCTGATCCCCTAG_ACCCAAGAGTCCAGGTACCTCTTCCCTTCCTT GA G BAX Ensembl:ENSG00000087088 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:48955496..48955675 26863410 MeRIP-seq:(Medium) rs1555795208 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2568534,Human_RBP_ID_5130558,Human_RBP_ID_5372014,Human_RBP_ID_8491741,Human_RBP_ID_13493224,Human_RBP_ID_17081999,Human_RBP_ID_19093913 Human_Splice_Rec_2028059,Human_Splice_Rec_2028069,Human_Splice_Rec_2028095,Human_Splice_Rec_2028107,Human_Splice_Rec_2028117,Human_Splice_Rec_2028137 RMVar_hsa_circ_127888,RMVar_hsa_circ_195747 70157 RMVar_ID_70157 Human_SNP_ID_668196500 m1A Human chr19 + 48956140 48956140 48956140 CTCCTTATCTTTAGTGTGCGGTGGATGCGGGAATTTTCCACCATCAGCCTGATGCCTGCTCCCCG CTCCTTATCTTTAGTGTGCGGTGGATGCGGGAGTTTTCCACCATCAGCCTGATGCCTGCTCCCCG A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48956136..48956275 26863196 MeRIP-seq:(Medium) rs898830660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137302,Human_RBP_ID_20409986,Human_RBP_ID_22546206 RMVar_hsa_circ_84404,RMVar_hsa_circ_127888,RMVar_hsa_circ_80691,RMVar_hsa_circ_195747,RMVar_hsa_circ_195748,RMVar_hsa_circ_195749 70158 RMVar_ID_70158 Human_SNP_ID_668196823 m1A Human chr19 + 48957093 48957093 48957093 TGATCGGGGGGAAGAGGCATCTGGTAGAGGGAACAGCAAGTGCAAAGGCCCTGAGGTAGGACCAA TGATCGGGGGGAAGAGGCATCTGGTAGAGGGAGCAGCAAGTGCAAAGGCCCTGAGGTAGGACCAA A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48957088..48957205 26863196 MeRIP-seq:(Medium) rs1256486523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13493276 RMVar_hsa_circ_84404,RMVar_hsa_circ_127888,RMVar_hsa_circ_80691,RMVar_hsa_circ_195747,RMVar_hsa_circ_195748,RMVar_hsa_circ_124997,RMVar_hsa_circ_195749,RMVar_hsa_circ_16454,RMVar_hsa_circ_195750 70159 RMVar_ID_70159 Human_SNP_ID_668198098 m1A Human chr19 + 48961023 48961023 48961023 CCACTCCTCTGGGACCCTGGGCCTTCTGGAGCAGGTCACAGTGGTGCCCTCTCCCCATCTTCAGA CCACTCCTCTGGGACCCTGGGCCTTCTGGAGCGGGTCACAGTGGTGCCCTCTCCCCATCTTCAGA A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48961021..48961150 26863196 MeRIP-seq:(Medium) rs769368417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239304,Human_RBP_ID_5131408,Human_RBP_ID_8491748,Human_RBP_ID_17082001 RMVar_hsa_circ_84404,RMVar_hsa_circ_127888,RMVar_hsa_circ_80691,RMVar_hsa_circ_195747,RMVar_hsa_circ_195748,RMVar_hsa_circ_108081,RMVar_hsa_circ_124997,RMVar_hsa_circ_195749,RMVar_hsa_circ_195750,RMVar_hsa_circ_195751 70160 RMVar_ID_70160 Human_SNP_ID_668198585 m1A Human chr19 + 48962382 48962382 48962382 AGGTCGCTGGAGGGTGGCAGGCTGAGGACACCAGGGCGAGGGCCCACGGGAGAGGCCTCCTGAGC AGGTCGCTGGAGGGTGGCAGGCTGAGGACACCCGGGCGAGGGCCCACGGGAGAGGCCTCCTGAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48962333..48962435 26863196 MeRIP-seq:(Medium) rs1255429563 Functional Loss SNV dbSNP153 33..33 33 - - - 70161 RMVar_ID_70161 Human_SNP_ID_668199504 m1A Human chr19 + 48965374 48965374 48965374 TTCAACAGTGTTTGGACGGAACAGATCCGGGGACTCTCTTCCAGCCTCCGACCGCCCTCCGATTT TTCAACAGTGTTTGGACGGAACAGATCCGGGGTCTCTCTTCCAGCCTCCGACCGCCCTCCGATTT A T FTL Ensembl:ENSG00000087086 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr19:48965276..48965551;chr19:48965301..48965548;chr19:48965276..48965558;chr19:48965301..48965575 26863196,32194978 MeRIP-seq:(Medium) rs1463766648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239296,Human_RBP_ID_525121,Human_RBP_ID_1017477,Human_RBP_ID_1569466,Human_RBP_ID_4557647,Human_RBP_ID_5421739,Human_RBP_ID_5443664,Human_RBP_ID_5469032,Human_RBP_ID_5499936,Human_RBP_ID_6778355,Human_RBP_ID_8098042,Human_RBP_ID_8491756,Human_RBP_ID_17501126,Human_RBP_ID_17929178,Human_RBP_ID_18200574,Human_RBP_ID_18208662,Human_RBP_ID_18737219,Human_RBP_ID_20349596,Human_RBP_ID_23131609,Human_RBP_ID_23804056,Human_RBP_ID_26749511,Human_RBP_ID_27276841,Human_RBP_ID_27470192 Human_miRNA_ID_2716411,Human_miRNA_ID_3052396 RMVar_hsa_circ_76881,RMVar_hsa_circ_123826,RMVar_hsa_circ_113700,RMVar_hsa_circ_195753,RMVar_hsa_circ_195754,RMVar_hsa_circ_195752 70162 RMVar_ID_70162 Human_SNP_ID_668199519 m1A Human chr19 + 48965403 48965403 48965403 GGGACTCTCTTCCAGCCTCCGACCGCCCTCCGATTTCCTCTCCGCTTGCAACCTCCGGGACCATC GGGACTCTCTTCCAGCCTCCGACCGCCCTCCGGTTTCCTCTCCGCTTGCAACCTCCGGGACCATC A G FTL Ensembl:ENSG00000087086 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:48965301..48965450 26863410 MeRIP-seq:(Medium) rs11553258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239296,Human_RBP_ID_270028,Human_RBP_ID_525122,Human_RBP_ID_1373966,Human_RBP_ID_1569468,Human_RBP_ID_3574938,Human_RBP_ID_4571662,Human_RBP_ID_5275441,Human_RBP_ID_5443333,Human_RBP_ID_5469034,Human_RBP_ID_5499937,Human_RBP_ID_8491756,Human_RBP_ID_17270213,Human_RBP_ID_17385120,Human_RBP_ID_17501127,Human_RBP_ID_18208663,Human_RBP_ID_18737219,Human_RBP_ID_20349597,Human_RBP_ID_22533195,Human_RBP_ID_22811612,Human_RBP_ID_23804057,Human_RBP_ID_26475094,Human_RBP_ID_26993266,Human_RBP_ID_27157773,Human_RBP_ID_27276842,Human_RBP_ID_27470192 RMVar_hsa_circ_76881,RMVar_hsa_circ_123826,RMVar_hsa_circ_113700,RMVar_hsa_circ_195753,RMVar_hsa_circ_195754,RMVar_hsa_circ_195752 70163 RMVar_ID_70163 Human_SNP_ID_668199993 m1A Human chr19 - 48966408 48966408 48966408 TGGTTGGGTAGCCATGGATGCAGCGGGTACGTACATGGGGGTCCGTGCGGGCAGAACCCAGGGCA TGGTTGGGTAGCCATGGATGCAGCGGGTACGTGCATGGGGGTCCGTGCGGGCAGAACCCAGGGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48966357..48966844 26863196 MeRIP-seq:(Medium) rs1371561306 Functional Loss SNV dbSNP153 33..33 33 - - - 70164 RMVar_ID_70164 Human_SNP_ID_668200151 m1A Human chr19 + 48966751 48966751 48966751 CTCTCAAGCACGACTAAGAGCCTTCTGAGCCCAGCGACTTCTGAAGGGCCCCTTGCAAAGTAATA CTCTCAAGCACGACTAAGAGCCTTCTGAGCCCGGCGACTTCTGAAGGGCCCCTTGCAAAGTAATA A G FTL Ensembl:ENSG00000087086 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:48966701..48966875 32194978 MeRIP-seq:(Medium) rs756977598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525143,Human_RBP_ID_1890822,Human_RBP_ID_8491774,Human_RBP_ID_13493433 Human_miRNA_ID_2555261 RMVar_hsa_circ_76881,RMVar_hsa_circ_113700,RMVar_hsa_circ_108653,RMVar_hsa_circ_195753,RMVar_hsa_circ_195754,RMVar_hsa_circ_105785,RMVar_hsa_circ_121492,RMVar_hsa_circ_99131,RMVar_hsa_circ_195755,RMVar_hsa_circ_195756,RMVar_hsa_circ_195757,RMVar_hsa_circ_195758 70165 RMVar_ID_70165 Human_SNP_ID_668200975 m1A Human chr19 + 48969250 48969249 48969251 AGCAGCACCCCTCTGCATCCTCTCTCTGGAGCAGAGAGGCAGGACAGGCGGGGAGTGTGGTGGGG AGCAGCACCCCTCTGCATCCTCTCTCTGGAGC__AGAGGCAGGACAGGCGGGGAGTGTGGTGGGG CAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:48969164..48969312 26863196 MeRIP-seq:(Medium) rs1250443178 Functional Loss DEL dbSNP153 33..34 33 - - - 70166 RMVar_ID_70166 Human_SNP_ID_668201045 m1A Human chr19 - 48969376 48969376 48969376 CTGCACCTCCTCCACCAGCGGCAGCAAGCGCAACTCTGTGGACACGGCCACCTCCAGCTCACTCA CTGCACCTCCTCCACCAGCGGCAGCAAGCGCACCTCTGTGGACACGGCCACCTCCAGCTCACTCA T G GYS1 Ensembl:ENSG00000104812 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48969325..48969422 26863196 MeRIP-seq:(Medium) rs768653661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4541561,Human_RBP_ID_8836212,Human_RBP_ID_27470217 RMVar_hsa_circ_195759 70167 RMVar_ID_70167 Human_SNP_ID_668201067 m1A Human chr19 + 48969410 48969410 48969410 GCGCTTGCTGCCGCTGGTGGAGGAGGTGCAGGACGCTCGGCGCGGCCACTCTGGTGCACGGATGT GCGCTTGCTGCCGCTGGTGGAGGAGGTGCAGGGCGCTCGGCGCGGCCACTCTGGTGCACGGATGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48969072..48969573 26863196 MeRIP-seq:(Medium) rs147627546 Functional Loss SNV dbSNP153 33..33 33 - - - 70168 RMVar_ID_70168 Human_SNP_ID_668206747 m1A Human chr19 + 48987505 48987500 48987505 AGATGTCTATAGACTTAAGCCTCAGCTCTCTTATCTTCTGTTTCCATATCTGCTGCTAATTTCTC AGATGTCTATAGACTTAAGCCTCAGCTC_____TCTTCTGTTTCCATATCTGCTGCTAATTTCTC CTCTTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48987496..48987636 26863196 MeRIP-seq:(Medium) rs1330701819 Functional Loss DEL dbSNP153 29..33 33 - - - 70169 RMVar_ID_70169 Human_SNP_ID_668207854 m1A Human chr19 + 48991112 48991112 48991112 CTCATACTTGCCATCTGTCTGTCCATTCGCCCATGTCTGGGATCCACCCACCCACTTCCAGGCCC CTCATACTTGCCATCTGTCTGTCCATTCGCCCGTGTCTGGGATCCACCCACCCACTTCCAGGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48991019..48991473 26863196 MeRIP-seq:(Medium) rs895269097 Functional Loss SNV dbSNP153 33..33 33 - - - 70170 RMVar_ID_70170 Human_SNP_ID_668208293 m1A Human chr19 - 48992808 48992808 48992808 GGGTGGGAGAGGGATGGTTCGTTTGACTTAAGATGAAAGGAGGCTGGAAGCCCGGGTTCTGGGTC GGGTGGGAGAGGGATGGTTCGTTTGACTTAAGGTGAAAGGAGGCTGGAAGCCCGGGTTCTGGGTC T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48992386..48993275 26863196 MeRIP-seq:(Medium) rs1364918382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557648,Human_RBP_ID_5191715,Human_RBP_ID_5320513,Human_RBP_ID_8197908,Human_RBP_ID_9425399,Human_RBP_ID_17190840,Human_RBP_ID_21980033,Human_RBP_ID_22975127,Human_RBP_ID_23279075,Human_RBP_ID_23804076 70171 RMVar_ID_70171 Human_SNP_ID_668208796 m1A Human chr19 - 48993923 48993914 48993923 TCGCTCCTCACCCTCCATGCACCCACACTTACAACGGTTGCCATGATGCTCACCAACTGCCAGAG TCGCTCCTCACCCTCCATGCACCCACACTTAC_________CATGATGCTCACCAACTGCCAGAG GGCAACCGTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48993893..48994245 26863196 MeRIP-seq:(Medium) rs778941221 Functional Loss DEL dbSNP153 33..41 33 - - - 70172 RMVar_ID_70172 Human_SNP_ID_668208799 m1A Human chr19 - 48993923 48993923 48993923 TCGCTCCTCACCCTCCATGCACCCACACTTACAACGGTTGCCATGATGCTCACCAACTGCCAGAG TCGCTCCTCACCCTCCATGCACCCACACTTACTACGGTTGCCATGATGCTCACCAACTGCCAGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48993893..48994245 26863196 MeRIP-seq:(Medium) rs547533762 Functional Loss SNV dbSNP153 33..33 33 - - - 70173 RMVar_ID_70173 Human_SNP_ID_668210259 m1A Human chr19 - 48999304 48999304 48999304 GACTTTGGTTGTGGCTGTCTGGGGGTGCAAGAAGATGTGTCAGAGGACTAGTGTGGTCCCAGCTT GACTTTGGTTGTGGCTGTCTGGGGGTGCAAGAGGATGTGTCAGAGGACTAGTGTGGTCCCAGCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48999301..48999375 26863196 MeRIP-seq:(Medium) rs753078286 Functional Loss SNV dbSNP153 33..33 33 - - - 70174 RMVar_ID_70174 Human_SNP_ID_668211622 m1A Human chr19 + 49004335 49004335 49004335 GGCGGCACGGCGGGCGGCTGGCGTGGTGCTGGAGATGATCCGGGAAGGGAAGATTGCCGGTCGGG GGCGGCACGGCGGGCGGCTGGCGTGGTGCTGGGGATGATCCGGGAAGGGAAGATTGCCGGTCGGG A G RUVBL2 Ensembl:ENSG00000183207 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49004276..49004375 26863196 MeRIP-seq:(Medium) rs537873608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240745,Human_RBP_ID_3955351,Human_RBP_ID_4541645,Human_RBP_ID_17935052,Human_RBP_ID_18995253,Human_RBP_ID_22446925,Human_RBP_ID_26336570 Human_Splice_Rec_2028246,Human_Splice_Rec_2028247,Human_Splice_Rec_2028270,Human_Splice_Rec_2028271,Human_Splice_Rec_2028280,Human_Splice_Rec_2028281,Human_Splice_Rec_2028312,Human_Splice_Rec_2028318,Human_Splice_Rec_2028319,Human_Splice_Rec_2028337,Human_Splice_Rec_2028364,Human_Splice_Rec_2028365,Human_Splice_Rec_2028394,Human_Splice_Rec_2028395,Human_Splice_Rec_2028410,Human_Splice_Rec_2028411,Human_Splice_Rec_2028431 RMVar_hsa_circ_97413,RMVar_hsa_circ_102952,RMVar_hsa_circ_195775,RMVar_hsa_circ_99196,RMVar_hsa_circ_195774,RMVar_hsa_circ_87747,RMVar_hsa_circ_119600,RMVar_hsa_circ_195776,RMVar_hsa_circ_195778,RMVar_hsa_circ_91489,RMVar_hsa_circ_195777,RMVar_hsa_circ_85789,RMVar_hsa_circ_195779,RMVar_hsa_circ_318708,RMVar_hsa_circ_195780 70175 RMVar_ID_70175 Human_SNP_ID_668213895 m1A Human chr19 + 49011225 49011225 49011225 TGCTGTTCATCGACGAGGTCCACATGCTGGACATCGAGAGCTTCTCCTTCCTCAACCGGGCCCTG TGCTGTTCATCGACGAGGTCCACATGCTGGACGTCGAGAGCTTCTCCTTCCTCAACCGGGCCCTG A G RUVBL2 Ensembl:ENSG00000183207 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49011076..49011355 26863196 MeRIP-seq:(Medium) rs1348736244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240748,Human_RBP_ID_525175,Human_RBP_ID_1569490,Human_RBP_ID_18192395,Human_RBP_ID_18737258,Human_RBP_ID_18995255,Human_RBP_ID_19093936,Human_RBP_ID_22449585,Human_RBP_ID_26817825 Human_Splice_Rec_2028260,Human_Splice_Rec_2028261,Human_Splice_Rec_2028294,Human_Splice_Rec_2028295,Human_Splice_Rec_2028350,Human_Splice_Rec_2028351,Human_Splice_Rec_2028378,Human_Splice_Rec_2028379,Human_Splice_Rec_2028422,Human_Splice_Rec_2028423,Human_Splice_Rec_2028444,Human_Splice_Rec_2028445 Human_miRNA_ID_2621986 RMVar_hsa_circ_11468,RMVar_hsa_circ_84280,RMVar_hsa_circ_195775,RMVar_hsa_circ_99196,RMVar_hsa_circ_87747,RMVar_hsa_circ_195778,RMVar_hsa_circ_91489,RMVar_hsa_circ_112216,RMVar_hsa_circ_195779,RMVar_hsa_circ_96109,RMVar_hsa_circ_118292,RMVar_hsa_circ_195783,RMVar_hsa_circ_195784,RMVar_hsa_circ_288483,RMVar_hsa_circ_195785,RMVar_hsa_circ_123695,RMVar_hsa_circ_195786,RMVar_hsa_circ_195787,RMVar_hsa_circ_195788,RMVar_hsa_circ_78539,RMVar_hsa_circ_195790,RMVar_hsa_circ_123629,RMVar_hsa_circ_92318,RMVar_hsa_circ_195791,RMVar_hsa_circ_76217,RMVar_hsa_circ_115094,RMVar_hsa_circ_195793,RMVar_hsa_circ_195794,RMVar_hsa_circ_195795 70176 RMVar_ID_70176 Human_SNP_ID_668214985 m1A Human chr19 - 49014991 49014991 49014991 CACCTGCAAGCAGTGGGGGACAGGGGTGGCTCAGCCGGGGCCCAGCCTCTGACTGCAGCAGAAGT CACCTGCAAGCAGTGGGGGACAGGGGTGGCTCGGCCGGGGCCCAGCCTCTGACTGCAGCAGAAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49014983..49015119 26863196 MeRIP-seq:(Medium) rs375023511 Functional Loss SNV dbSNP153 33..33 33 - - - 70177 RMVar_ID_70177 Human_SNP_ID_668215045 m1A Human chr19 - 49015134 49015134 49015134 AATTCGGCCGGCTGACCTTGCGTTTCCGGCACACCAAGCTGGCAGCTGTGATGAGCTGGATGGCG AATTCGGCCGGCTGACCTTGCGTTTCCGGCACGCCAAGCTGGCAGCTGTGATGAGCTGGATGGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49015001..49015270 32194978 MeRIP-seq:(Medium) rs1273856911 Functional Loss SNV dbSNP153 33..33 33 - - - 70178 RMVar_ID_70178 Human_SNP_ID_668242661 m1A Human chr19 + 49085533 49085533 49085533 GCTTAGCGGGCGACGGAATCAGACGGACGTGGACGCCCCCGGAGTGGAAGCCGAAGCAGGAGTTG GCTTAGCGGGCGACGGAATCAGACGGACGTGGGCGCCCCCGGAGTGGAAGCCGAAGCAGGAGTTG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49085468..49086575 32194978 MeRIP-seq:(Medium) rs550686001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55007,Human_RBP_ID_525192,Human_RBP_ID_1017490,Human_RBP_ID_1569526,Human_RBP_ID_4541728,Human_RBP_ID_6778449,Human_RBP_ID_8491827,Human_RBP_ID_8836226,Human_RBP_ID_9089175,Human_RBP_ID_9329115,Human_RBP_ID_9382757,Human_RBP_ID_13493937,Human_RBP_ID_18421435,Human_RBP_ID_18737286,Human_RBP_ID_22975147,Human_RBP_ID_23804144,Human_RBP_ID_26993324 70179 RMVar_ID_70179 Human_SNP_ID_668242682 m1A Human chr19 + 49085575 49085575 49085575 AGTGGAAGCCGAAGCAGGAGTTGTTGTTGCTGAGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGAC AGTGGAAGCCGAAGCAGGAGTTGTTGTTGCTGGGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGAC A G SNRNP70 Ensembl:ENSG00000104852 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:49085479..49087658 26863196 MeRIP-seq:(Medium) rs894221807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55007,Human_RBP_ID_241195,Human_RBP_ID_525193,Human_RBP_ID_1569526,Human_RBP_ID_3955354,Human_RBP_ID_4541731,Human_RBP_ID_8491829,Human_RBP_ID_8836227,Human_RBP_ID_9329115,Human_RBP_ID_9382758,Human_RBP_ID_18421436,Human_RBP_ID_18737287,Human_RBP_ID_18998399,Human_RBP_ID_22070425,Human_RBP_ID_22237544,Human_RBP_ID_22811636,Human_RBP_ID_23804146,Human_RBP_ID_26475100,Human_RBP_ID_26993326 Human_Splice_Rec_2028561,Human_Splice_Rec_2028581,Human_Splice_Rec_2028593,Human_Splice_Rec_2028599,Human_Splice_Rec_2028617,Human_Splice_Rec_2028637,Human_Splice_Rec_2028655 70180 RMVar_ID_70180 Human_SNP_ID_668242695 m1A Human chr19 + 49085606 49085606 49085606 GAGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGACAGACGCCAGAGCGAGGAGGGCGCTACGCGGT GAGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGCCAGACGCCAGAGCGAGGAGGGCGCTACGCGGT A C SNRNP70 Ensembl:ENSG00000104852 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49085419..49086616 26863196 MeRIP-seq:(Medium) rs1036402610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241195,Human_RBP_ID_773498,Human_RBP_ID_3955354,Human_RBP_ID_4541734,Human_RBP_ID_8840169,Human_RBP_ID_9329115,Human_RBP_ID_9381271,Human_RBP_ID_13493940,Human_RBP_ID_18421436,Human_RBP_ID_18998400,Human_RBP_ID_22070425 Human_Splice_Rec_2028561,Human_Splice_Rec_2028581,Human_Splice_Rec_2028593,Human_Splice_Rec_2028599,Human_Splice_Rec_2028617,Human_Splice_Rec_2028637,Human_Splice_Rec_2028655 70181 RMVar_ID_70181 Human_SNP_ID_668242696 m1A Human chr19 + 49085606 49085606 49085606 GAGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGACAGACGCCAGAGCGAGGAGGGCGCTACGCGGT GAGGGGCTGCCGCAGCCGCCGCGAGCCTCCGGGCAGACGCCAGAGCGAGGAGGGCGCTACGCGGT A G SNRNP70 Ensembl:ENSG00000104852 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49085419..49086616 26863196 MeRIP-seq:(Medium) rs1036402610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241195,Human_RBP_ID_773498,Human_RBP_ID_3955354,Human_RBP_ID_4541734,Human_RBP_ID_8840169,Human_RBP_ID_9329115,Human_RBP_ID_9381271,Human_RBP_ID_13493940,Human_RBP_ID_18421436,Human_RBP_ID_18998400,Human_RBP_ID_22070425 Human_Splice_Rec_2028561,Human_Splice_Rec_2028581,Human_Splice_Rec_2028593,Human_Splice_Rec_2028599,Human_Splice_Rec_2028617,Human_Splice_Rec_2028637,Human_Splice_Rec_2028655 70182 RMVar_ID_70182 Human_SNP_ID_668242708 m1A Human chr19 - 49085631 49085631 49085631 TCGGGCCACTCAGTCACACTCACTCACCGCGTAGCGCCCTCCTCGCTCTGGCGTCTGTCCGGAGG TCGGGCCACTCAGTCACACTCACTCACCGCGTGGCGCCCTCCTCGCTCTGGCGTCTGTCCGGAGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:49085492..49085680 26863410 MeRIP-seq:(Medium) rs1294716215 Functional Loss SNV dbSNP153 33..33 33 - - - 70183 RMVar_ID_70183 Human_SNP_ID_668243021 m1A Human chr19 - 49086357 49086357 49086357 GGACAGCCTTAGGTTAGATCGGGTCTGCACAGAGAAAGCCCCTGTTACTCCTTGACTCTCAAAAT GGACAGCCTTAGGTTAGATCGGGTCTGCACAGCGAAAGCCCCTGTTACTCCTTGACTCTCAAAAT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:49086352..49086563 26863410 MeRIP-seq:(Medium) rs1179767706 Functional Loss SNV dbSNP153 33..33 33 - - - 70184 RMVar_ID_70184 Human_SNP_ID_668243078 m1A Human chr19 + 49086501 49086501 49086501 ATTCCATACCTGCCACCCCTGGAGAAACTGCCACATGAAAAACACCACAATCAACCTTATTGTGG ATTCCATACCTGCCACCCCTGGAGAAACTGCCGCATGAAAAACACCACAATCAACCTTATTGTGG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49086451..49086668 26863196 MeRIP-seq:(Medium) rs956289957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569532,Human_RBP_ID_2568584,Human_RBP_ID_3574970,Human_RBP_ID_3957305,Human_RBP_ID_9381274,Human_RBP_ID_13493985,Human_RBP_ID_18737291 Human_Splice_Rec_2028562,Human_Splice_Rec_2028563,Human_Splice_Rec_2028594,Human_Splice_Rec_2028595,Human_Splice_Rec_2028600,Human_Splice_Rec_2028601,Human_Splice_Rec_2028618,Human_Splice_Rec_2028619,Human_Splice_Rec_2028638,Human_Splice_Rec_2028639,Human_Splice_Rec_2028656,Human_Splice_Rec_2028657,Human_Splice_Rec_2028675,Human_Splice_Rec_2028683 Human_miRNA_ID_1012604,Human_miRNA_ID_1294613,Human_miRNA_ID_1298588 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_314698,RMVar_hsa_circ_195800,RMVar_hsa_circ_195801 70185 RMVar_ID_70185 Human_SNP_ID_668244235 m1A Human chr19 + 49090314 49090314 49090314 TGTTCCCAGGACCCTCGAGATGCCCCTCCTCCAACTCGTGCTGAAACCCGAGAGGAGCGCATGGA TGTTCCCAGGACCCTCGAGATGCCCCTCCTCCGACTCGTGCTGAAACCCGAGAGGAGCGCATGGA A G SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49090301..49090375 26863196 MeRIP-seq:(Medium) rs1368237342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525197,Human_RBP_ID_913939,Human_RBP_ID_4541741,Human_RBP_ID_9381277,Human_RBP_ID_17929221,Human_RBP_ID_18441790,Human_RBP_ID_18737299,Human_RBP_ID_18998402,Human_RBP_ID_23804152 Human_Splice_Rec_2028564,Human_Splice_Rec_2028565,Human_Splice_Rec_2028582,Human_Splice_Rec_2028583,Human_Splice_Rec_2028596,Human_Splice_Rec_2028597,Human_Splice_Rec_2028602,Human_Splice_Rec_2028603,Human_Splice_Rec_2028620,Human_Splice_Rec_2028621,Human_Splice_Rec_2028640,Human_Splice_Rec_2028641,Human_Splice_Rec_2028658,Human_Splice_Rec_2028659,Human_Splice_Rec_2028678,Human_Splice_Rec_2028679,Human_Splice_Rec_2028684,Human_Splice_Rec_2028685 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801,RMVar_hsa_circ_269415,RMVar_hsa_circ_299522,RMVar_hsa_circ_369069,RMVar_hsa_circ_195802 70186 RMVar_ID_70186 Human_SNP_ID_668246720 m1A Human chr19 + 49098692 49098692 49098692 TCCAAGCTCCGGAGAGAGTTTGAGGTGTACGGACCTATCAAAAGAGTAAGTGGAGTGGGTCAGGG TCCAAGCTCCGGAGAGAGTTTGAGGTGTACGGTCCTATCAAAAGAGTAAGTGGAGTGGGTCAGGG A T SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49098626..49098725 26863196 MeRIP-seq:(Medium) rs1018236467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525198,Human_RBP_ID_911766,Human_RBP_ID_1569543,Human_RBP_ID_1890860,Human_RBP_ID_3957311,Human_RBP_ID_6778501,Human_RBP_ID_9381280,Human_RBP_ID_13494287,Human_RBP_ID_17935486,Human_RBP_ID_18737310,Human_RBP_ID_18995259,Human_RBP_ID_23804162,Human_RBP_ID_26334948 Human_Splice_Rec_2028570,Human_Splice_Rec_2028571,Human_Splice_Rec_2028588,Human_Splice_Rec_2028589,Human_Splice_Rec_2028608,Human_Splice_Rec_2028609,Human_Splice_Rec_2028626,Human_Splice_Rec_2028627,Human_Splice_Rec_2028646,Human_Splice_Rec_2028647,Human_Splice_Rec_2028664,Human_Splice_Rec_2028665,Human_Splice_Rec_2028690,Human_Splice_Rec_2028691 RMVar_hsa_circ_369069,RMVar_hsa_circ_195804,RMVar_hsa_circ_333511 70187 RMVar_ID_70187 Human_SNP_ID_668247539 m1A Human chr19 - 49101466 49101466 49101466 GGGCAGGGCTCGGCGGGAGGTACTCACAGTGCATGTCTCGCTCGTGTTCGTACTCGATGAAGGCA GGGCAGGGCTCGGCGGGAGGTACTCACAGTGCGTGTCTCGCTCGTGTTCGTACTCGATGAAGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49101366..49101543;chr19:49101366..49101531;chr19:49098426..49101538;chr19:49101376..49101475 26863196 MeRIP-seq:(Medium) rs762290154 Functional Loss SNV dbSNP153 33..33 33 - - - 70188 RMVar_ID_70188 Human_SNP_ID_668248612 m1A Human chr19 - 49104418 49104418 49104418 CCATCTCAGCGTCTGCTTCCTCTCAGCGCCCCAACCACTCCTGGTCGGGGGAGACGTCCACCCTC CCATCTCAGCGTCTGCTTCCTCTCAGCGCCCCCACCACTCCTGGTCGGGGGAGACGTCCACCCTC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49104326..49104550 26863196 MeRIP-seq:(Medium) rs571409315 Functional Loss SNV dbSNP153 33..33 33 - - - 70189 RMVar_ID_70189 Human_SNP_ID_668249714 m1A Human chr19 + 49107836 49107834 49107837 CTCCCCGCTTCCGCACAGGGACCGGGACCGGGACCGTGAGCGGGAGCGCAGAGAGCGGAGCCGGG CTCCCCGCTTCCGCACAGGGACCGGGACCGG___CGTGAGCGGGAGCGCAGAGAGCGGAGCCGGG GGAC G SNRNP70 Ensembl:ENSG00000104852 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49104626..49108600 32194978 MeRIP-seq:(Medium) rs1555739178 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_55026,Human_RBP_ID_4541824,Human_RBP_ID_8836237,Human_RBP_ID_9381285,Human_RBP_ID_18998416,Human_RBP_ID_22592321,Human_RBP_ID_22977502,Human_RBP_ID_25429869,Human_RBP_ID_26336588 Human_Splice_Rec_2028580,Human_Splice_Rec_2028616,Human_Splice_Rec_2028636,Human_Splice_Rec_2028654,Human_Splice_Rec_2028674,Human_Splice_Rec_2028696 70190 RMVar_ID_70190 Human_SNP_ID_668249804 m1A Human chr19 + 49108034 49108028 49108034 AAGCAGCCGGAGTCGGGAGCGGGCCCGGCGGGAGCGGGAGCGCAAGGAGGAGCTGCGTGGCGGCG AAGCAGCCGGAGTCGGGAGCGGGCCCG______GCGGGAGCGCAAGGAGGAGCTGCGTGGCGGCG GGCGGGA G SNRNP70 Ensembl:ENSG00000104852 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49103893..49108625;chr19:49104177..49108625;chr19:49104578..49108625 26863196 MeRIP-seq:(Medium) rs966533040 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_241213,Human_RBP_ID_9293848,Human_RBP_ID_9329117,Human_RBP_ID_9382775,Human_RBP_ID_18470641,Human_RBP_ID_22446940,Human_RBP_ID_22533460,Human_RBP_ID_22665767,Human_RBP_ID_22977794 70191 RMVar_ID_70191 Human_SNP_ID_668249966 m1A Human chr19 + 49108262 49108262 49108262 CCGGGATCGTGACCGTGACCGTGACCGCGAGCACAAACGGGGGGAGCGGGGCAGTGAGCGGGGCA CCGGGATCGTGACCGTGACCGTGACCGCGAGCGCAAACGGGGGGAGCGGGGCAGTGAGCGGGGCA A G SNRNP70 Ensembl:ENSG00000104852 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:49107882..49108433 26863196 MeRIP-seq:(Medium) rs759622194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525210,Human_RBP_ID_1017497,Human_RBP_ID_5117043,Human_RBP_ID_17655657,Human_RBP_ID_18165819,Human_RBP_ID_18737356,Human_RBP_ID_22426350,Human_RBP_ID_22446942,Human_RBP_ID_27473583 70192 RMVar_ID_70192 Human_SNP_ID_668253376 m1A Human chr19 - 49118410 49118410 49118410 AAATAAAGTGCCAGGAACAATAAATACTGTACAGGAAGAGAGTGCACGTGAACGTCCAGATCTGT AAATAAAGTGCCAGGAACAATAAATACTGTACGGGAAGAGAGTGCACGTGAACGTCCAGATCTGT T C C19orf73 Ensembl:ENSG00000221916 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49118331..49118409 26863196 MeRIP-seq:(Medium) rs1214636198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1399539 70193 RMVar_ID_70193 Human_SNP_ID_668253728 m1A Human chr19 - 49119101 49119101 49119101 CCTGGAGCGAGTAGCGCGCGGCGTGGAACGCGAGTCGCGACCCCGGCTCCCGGCAGTGGCGCGCA CCTGGAGCGAGTAGCGCGCGGCGTGGAACGCGCGTCGCGACCCCGGCTCCCGGCAGTGGCGCGCA T G C19orf73 Ensembl:ENSG00000221916 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49118955..49119116 26863196 MeRIP-seq:(Medium) rs1198052393 Functional Loss SNV dbSNP153 33..33 33 - - - 70194 RMVar_ID_70194 Human_SNP_ID_668253901 m1A Human chr19 - 49119437 49119436 49119437 CCTCCCCCCGCGAGGCCGCAGCCGCCAGATCCAGGGGTGCCCACCAGCGCCCCCCAAATCCCACC CCTCCCCCCGCGAGGCCGCAGCCGCCAGATCC_GGGGTGCCCACCAGCGCCCCCCAAATCCCACC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49119399..49119475 26863196 MeRIP-seq:(Medium) rs1393374234 Functional Loss DEL dbSNP153 33..33 33 - - - 70195 RMVar_ID_70195 Human_SNP_ID_668253902 m1A Human chr19 - 49119437 49119437 49119437 CCTCCCCCCGCGAGGCCGCAGCCGCCAGATCCAGGGGTGCCCACCAGCGCCCCCCAAATCCCACC CCTCCCCCCGCGAGGCCGCAGCCGCCAGATCCCGGGGTGCCCACCAGCGCCCCCCAAATCCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49119399..49119475 26863196 MeRIP-seq:(Medium) rs1292121904 Functional Loss SNV dbSNP153 33..33 33 - - - 70196 RMVar_ID_70196 Human_SNP_ID_668254009 m1A Human chr19 + 49119686 49119686 49119686 GGCCCCCCCACTCCACCCCACGTCCCTCCTGCAGCCCAGCTCCGCCCGCAGCCGCCGCGGACCAG GGCCCCCCCACTCCACCCCACGTCCCTCCTGCCGCCCAGCTCCGCCCGCAGCCGCCGCGGACCAG A C PPFIA3 Ensembl:ENSG00000177380 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49119636..49125364 32194978 MeRIP-seq:(Medium) rs1157912395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2028743,Human_Splice_Rec_2028801 70197 RMVar_ID_70197 Human_SNP_ID_668256475 m1A Human chr19 - 49128648 49128648 49128648 GTACAGAAAAGAGAAAAGTTATGGAGACAGGGAGGAAGGAGTGGCACCAGAGTGGGAGACCAGCC GTACAGAAAAGAGAAAAGTTATGGAGACAGGGGGGAAGGAGTGGCACCAGAGTGGGAGACCAGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49128613..49128722 26863196 MeRIP-seq:(Medium) rs1376685151 Functional Loss SNV dbSNP153 33..33 33 - - - 70198 RMVar_ID_70198 Human_SNP_ID_668256964 m1A Human chr19 - 49130487 49130487 49130487 CCAGCTGGCTCATCTGACGGCACAGCACCGCCAGGCGCTCCCGCAGCTGGCACACCTCGGCGCGC CCAGCTGGCTCATCTGACGGCACAGCACCGCCGGGCGCTCCCGCAGCTGGCACACCTCGGCGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:49130437..49130522;chr19:49130448..49130533 26863196 MeRIP-seq:(Medium) rs530188851 Functional Loss SNV dbSNP153 33..33 33 - - - 70199 RMVar_ID_70199 Human_SNP_ID_668256984 m1A Human chr19 - 49130528 49130528 49130528 TGCCTTGCCCAGCTCACGGTGCGCGGTGCCCAACTCCTCCTCCAGCTGGCTCATCTGACGGCACA TGCCTTGCCCAGCTCACGGTGCGCGGTGCCCAGCTCCTCCTCCAGCTGGCTCATCTGACGGCACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49130401..49130575 26863196 MeRIP-seq:(Medium) rs780338052 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70200 RMVar_ID_70200 Human_SNP_ID_668258118 m1A Human chr19 - 49134020 49134020 49134020 TCTTCTCCCGCTGCCGGGCCTGCGCAAAGCAGAGCGGGGCGGGTTGTTAAGCCCACCCTGCCCAG TCTTCTCCCGCTGCCGGGCCTGCGCAAAGCAGGGCGGGGCGGGTTGTTAAGCCCACCCTGCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49134009..49134117 26863196 MeRIP-seq:(Medium) rs773917961 Functional Loss SNV dbSNP153 33..33 33 - - - 70201 RMVar_ID_70201 Human_SNP_ID_668262915 m1A Human chr19 + 49150017 49150017 49150017 TGTGACATCGGGAAGGGAAGTCCAAAGGGAGGAATCCTGGAGAGGAACAGGGAGGAGGGTGCTCC TGTGACATCGGGAAGGGAAGTCCAAAGGGAGGTATCCTGGAGAGGAACAGGGAGGAGGGTGCTCC A T PPFIA3 Ensembl:ENSG00000177380 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49149973..49150064 26863196 MeRIP-seq:(Medium) rs996599191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72616 70202 RMVar_ID_70202 Human_SNP_ID_668263018 m1A Human chr19 - 49150288 49150288 49150288 CCCGCTCTCCCCGGCGAGGCCACAGTCCGGGCAGGAGAGGGAACAGCCCAGCCTCGGGAAGATTC CCCGCTCTCCCCGGCGAGGCCACAGTCCGGGCCGGAGAGGGAACAGCCCAGCCTCGGGAAGATTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49150082..49150431 32194978 MeRIP-seq:(Medium) rs752566410 Functional Loss SNV dbSNP153 33..33 33 - - - 70203 RMVar_ID_70203 Human_SNP_ID_668263160 m1A Human chr19 - 49150749 49150749 49150749 GGGGACACGAGACACGGGGGAGGGAGAGGGGAACCCGCCCGCAGATGACCCGGGGGACCGGCGAC GGGGACACGAGACACGGGGGAGGGAGAGGGGACCCCGCCCGCAGATGACCCGGGGGACCGGCGAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49150727..49150828 32194978 MeRIP-seq:(Medium) rs8044 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8414,GWAS_ID_8415,GWAS_ID_8416,GWAS_ID_8417 70204 RMVar_ID_70204 Human_SNP_ID_668266040 m1A Human chr19 + 49157842 49157842 49157842 CCGGCGGAGGGAGCGCCGGGGCCCTGGGCTGCAGGAGGTTGCGGCGGCCGCGGCAGCATGGTGGT CCGGCGGAGGGAGCGCCGGGGCCCTGGGCTGCCGGAGGTTGCGGCGGCCGCGGCAGCATGGTGGT A C TRPM4 Ensembl:ENSG00000130529 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:49157771..49157924;chr19:49157780..49157962 26863196 MeRIP-seq:(Medium) rs1005815380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145858,Human_RBP_ID_5320518,Human_RBP_ID_18420964 Human_Splice_Rec_2029053,Human_Splice_Rec_2029061,Human_Splice_Rec_2029099,Human_Splice_Rec_2029101,Human_Splice_Rec_2029149,Human_Splice_Rec_2029193,Human_Splice_Rec_2029239,Human_Splice_Rec_2029285 70205 RMVar_ID_70205 Human_SNP_ID_668266077 m1A Human chr19 + 49157889 49157889 49157889 CCGCGGCAGCATGGTGGTGCCGGAGAAGGAGCAGGTGAGCGCCGGACCAGGGTCTGCGGGAGCGC CCGCGGCAGCATGGTGGTGCCGGAGAAGGAGCTGGTGAGCGCCGGACCAGGGTCTGCGGGAGCGC A T TRPM4 Ensembl:ENSG00000130529 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49157839..49158390 32194978 MeRIP-seq:(Medium) rs1057522811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145858,Human_RBP_ID_5320518,Human_RBP_ID_18420964,Human_RBP_ID_19093953 Human_Splice_Rec_2029053,Human_Splice_Rec_2029061,Human_Splice_Rec_2029099,Human_Splice_Rec_2029101,Human_Splice_Rec_2029149,Human_Splice_Rec_2029193,Human_Splice_Rec_2029239,Human_Splice_Rec_2029285 70206 RMVar_ID_70206 Human_SNP_ID_668273826 m1A Human chr19 - 49182725 49182725 49182725 GGACGCCTGGTCCAAAAGGTTGCGGATGAGCGAGTTGGAGGGCGCCGCGCTGTAGAGTTGGGCCA GGACGCCTGGTCCAAAAGGTTGCGGATGAGCGGGTTGGAGGGCGCCGCGCTGTAGAGTTGGGCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49182676..49188806 32194978 MeRIP-seq:(Medium) rs866431568 Functional Loss SNV dbSNP153 33..33 33 - - - 70207 RMVar_ID_70207 Human_SNP_ID_668282429 m1A Human chr19 + 49211232 49211232 49211232 GAGGCCCTGAGCCGCTCTGCCTTGCTGCCCCCAGGTGGGCCGCCACCCCCTGACCTGCCTGGGTC GAGGCCCTGAGCCGCTCTGCCTTGCTGCCCCCCGGTGGGCCGCCACCCCCTGACCTGCCTGGGTC A C TRPM4 Ensembl:ENSG00000130529 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49211014..49211240 32194978 MeRIP-seq:(Medium) rs1489000217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955380,Human_RBP_ID_23211343 Human_Splice_Rec_2029096,Human_Splice_Rec_2029097,Human_Splice_Rec_2029146,Human_Splice_Rec_2029147,Human_Splice_Rec_2029190,Human_Splice_Rec_2029191,Human_Splice_Rec_2029236,Human_Splice_Rec_2029237,Human_Splice_Rec_2029282,Human_Splice_Rec_2029283,Human_Splice_Rec_2029326,Human_Splice_Rec_2029327,Human_Splice_Rec_2029362,Human_Splice_Rec_2029363,Human_Splice_Rec_2029372,Human_Splice_Rec_2029374 RMVar_hsa_circ_195817,RMVar_hsa_circ_84899,RMVar_hsa_circ_35057 70208 RMVar_ID_70208 Human_SNP_ID_668282541 m1A Human chr19 - 49211587 49211587 49211587 ATGGACATGGGGCTCACCTCAAGGACAAGGCCACCAGGTGCGGGGGCCGAGGCCCAGATGAGCCT ATGGACATGGGGCTCACCTCAAGGACAAGGCCGCCAGGTGCGGGGGCCGAGGCCCAGATGAGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49211537..49211687 32194978 MeRIP-seq:(Medium) rs537199372 Functional Loss SNV dbSNP153 33..33 33 - - - 70209 RMVar_ID_70209 Human_SNP_ID_668309116 m1A Human chr19 + 49309585 49309585 49309585 AGCCAAAGGAGTAAGAGATTAGGAGATCAACAAGTAACAAATTGAGGTAAGGGCTAAAGCATCTG AGCCAAAGGAGTAAGAGATTAGGAGATCAACAGGTAACAAATTGAGGTAAGGGCTAAAGCATCTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49309483..49309625 26863196 MeRIP-seq:(Medium) rs141640658 Functional Loss SNV dbSNP153 33..33 33 - - - 70210 RMVar_ID_70210 Human_SNP_ID_668315404 m1A Human chr19 + 49335538 49335538 49335538 TGTGGTGAGTGGACCGCTTACCCCACTAGGTGAAGATGTCAGCCCAGGAGAGCTGCCTCAGCCTC TGTGGTGAGTGGACCGCTTACCCCACTAGGTGTAGATGTCAGCCCAGGAGAGCTGCCTCAGCCTC A T CD37 Ensembl:ENSG00000104894 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49335501..49335776 26863196 MeRIP-seq:(Medium) rs1261959144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20433045 Human_Splice_Rec_2029454,Human_Splice_Rec_2029455,Human_Splice_Rec_2029470,Human_Splice_Rec_2029471,Human_Splice_Rec_2029479,Human_Splice_Rec_2029491,Human_Splice_Rec_2029505,Human_Splice_Rec_2029525,Human_Splice_Rec_2029539,Human_Splice_Rec_2029549,Human_Splice_Rec_2029561,Human_Splice_Rec_2029575,Human_Splice_Rec_2029581 RMVar_hsa_circ_20559 70211 RMVar_ID_70211 Human_SNP_ID_668316321 m1A Human chr19 - 49338384 49338384 49338384 GATACCCGACAGGTGAATAGGAGTGCGAGACCATGTGAGTCTCATCGGGGGCGGGGTCCGGTGGA GATACCCGACAGGTGAATAGGAGTGCGAGACCGTGTGAGTCTCATCGGGGGCGGGGTCCGGTGGA T C AC011450.1 Ensembl:ENSG00000197813 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49338338..49338522 26863196 MeRIP-seq:(Medium) rs77439714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581516,Human_RBP_ID_8233515,Human_RBP_ID_9089224,Human_RBP_ID_9427571,Human_RBP_ID_18737400 70212 RMVar_ID_70212 Human_SNP_ID_668316367 m1A Human chr19 + 49338649 49338649 49338649 CCTCATACCCATCACCTTGTCCCCTGATCCCCAACATCATATGTCTCCAGTCCCGGTCCCTCTGA CCTCATACCCATCACCTTGTCCCCTGATCCCCCACATCATATGTCTCCAGTCCCGGTCCCTCTGA A C CD37 Ensembl:ENSG00000104894 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49337992..49338791 26863196 MeRIP-seq:(Medium) rs1214702732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195822,RMVar_hsa_circ_359378 70213 RMVar_ID_70213 Human_SNP_ID_668316886 m1A Human chr19 - 49340055 49340055 49340055 CAGGGCTGGCTGATGAGGCGGGAATAGCTGCTACAAGTGGGGGTAGAGGCTGAGAAGGAGTAAGG CAGGGCTGGCTGATGAGGCGGGAATAGCTGCTGCAAGTGGGGGTAGAGGCTGAGAAGGAGTAAGG T C AC011450.1 Ensembl:ENSG00000197813 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49339963..49340557 26863196 MeRIP-seq:(Medium) rs891532236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581522,Human_RBP_ID_5586708,Human_RBP_ID_9427573,Human_RBP_ID_17190892 70214 RMVar_ID_70214 Human_SNP_ID_668316972 m1A Human chr19 - 49340241 49340241 49340241 ATCGAGAGCGTCATGAACCCGAGCTATAGAGAAAGGAGATGAGGTCAGAGAAGTCGAAGGGGTGC ATCGAGAGCGTCATGAACCCGAGCTATAGAGAGAGGAGATGAGGTCAGAGAAGTCGAAGGGGTGC T C AC011450.1 Ensembl:ENSG00000197813 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49332262..49340507 26863196 MeRIP-seq:(Medium) rs376634983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525271,Human_RBP_ID_13495083,Human_RBP_ID_23804411 Human_Splice_Rec_2029445,Human_Splice_Rec_2029449 Human_miRNA_ID_3216238 70215 RMVar_ID_70215 Human_SNP_ID_668318959 m1A Human chr19 - 49347365 49347365 49347365 CTCCGACTTCTCACCCACGGCCAACCCTCCTCAGTACCAGAGGCACCTGTTCGTGCACATCAGCC CTCCGACTTCTCACCCACGGCCAACCCTCCTCGGTACCAGAGGCACCTGTTCGTGCACATCAGCC T C TEAD2 Ensembl:ENSG00000074219 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49347246..49347416 26863196 MeRIP-seq:(Medium) rs1568564277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2029752 RMVar_hsa_circ_57473,RMVar_hsa_circ_35678,RMVar_hsa_circ_80808,RMVar_hsa_circ_195824,RMVar_hsa_circ_378511,RMVar_hsa_circ_19944,RMVar_hsa_circ_84991,RMVar_hsa_circ_55206,RMVar_hsa_circ_333028,RMVar_hsa_circ_195828,RMVar_hsa_circ_364830,RMVar_hsa_circ_307475 70216 RMVar_ID_70216 Human_SNP_ID_668319280 m1A Human chr19 - 49348745 49348745 49348745 CGGGGCCTGGGCACCGCCCGGTTGCAGCTGGTAGAGTTCTCAGCCTTCGTGGAACCGCCAGATGC CGGGGCCTGGGCACCGCCCGGTTGCAGCTGGTGGAGTTCTCAGCCTTCGTGGAACCGCCAGATGC T C TEAD2 Ensembl:ENSG00000074219 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49347366..49348744 32194978 MeRIP-seq:(Medium) rs753750433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955381 Human_Splice_Rec_2029615,Human_Splice_Rec_2029637,Human_Splice_Rec_2029661,Human_Splice_Rec_2029683,Human_Splice_Rec_2029703,Human_Splice_Rec_2029725,Human_Splice_Rec_2029741,Human_Splice_Rec_2029751,Human_Splice_Rec_2029765 RMVar_hsa_circ_57473,RMVar_hsa_circ_35678,RMVar_hsa_circ_80808,RMVar_hsa_circ_195824,RMVar_hsa_circ_378511,RMVar_hsa_circ_19944,RMVar_hsa_circ_84991,RMVar_hsa_circ_55206,RMVar_hsa_circ_333028,RMVar_hsa_circ_195828,RMVar_hsa_circ_364830,RMVar_hsa_circ_307475 70217 RMVar_ID_70217 Human_SNP_ID_668320989 m1A Human chr19 - 49355174 49355174 49355174 GCCTCTGAGCTTTTCCAGTTTTGGTCTGGAGGATCTGGGCCCCCCTGGAATGTTCCAGAGTGAGT GCCTCTGAGCTTTTCCAGTTTTGGTCTGGAGGGTCTGGGCCCCCCTGGAATGTTCCAGAGTGAGT T C TEAD2 Ensembl:ENSG00000074219 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49351343..49355321 32194978 MeRIP-seq:(Medium) rs770660375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525296,Human_RBP_ID_18998441 Human_Splice_Rec_2029610,Human_Splice_Rec_2029611,Human_Splice_Rec_2029632,Human_Splice_Rec_2029633,Human_Splice_Rec_2029656,Human_Splice_Rec_2029657,Human_Splice_Rec_2029678,Human_Splice_Rec_2029679,Human_Splice_Rec_2029698,Human_Splice_Rec_2029699,Human_Splice_Rec_2029720,Human_Splice_Rec_2029721,Human_Splice_Rec_2029736,Human_Splice_Rec_2029737,Human_Splice_Rec_2029746,Human_Splice_Rec_2029747,Human_Splice_Rec_2029760,Human_Splice_Rec_2029761 RMVar_hsa_circ_57473,RMVar_hsa_circ_35678,RMVar_hsa_circ_80808,RMVar_hsa_circ_195824,RMVar_hsa_circ_19944,RMVar_hsa_circ_84991,RMVar_hsa_circ_88842,RMVar_hsa_circ_55206,RMVar_hsa_circ_195828,RMVar_hsa_circ_307475,RMVar_hsa_circ_11699,RMVar_hsa_circ_195830,RMVar_hsa_circ_62872,RMVar_hsa_circ_316401,RMVar_hsa_circ_316289,RMVar_hsa_circ_195831 70218 RMVar_ID_70218 Human_SNP_ID_668323003 m1A Human chr19 + 49362049 49362049 49362049 CTTCTCCGTAAGAAGGACCAAATGCCCCCCAGATTACACAAGGGGTCCTTCTCACTCCAAAGTGA CTTCTCCGTAAGAAGGACCAAATGCCCCCCAGGTTACACAAGGGGTCCTTCTCACTCCAAAGTGA A G DKKL1 Ensembl:ENSG00000104901 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49362039..49362404 26863196 MeRIP-seq:(Medium) rs1374685661 Functional Loss SNV dbSNP153 33..33 33 - - - 70219 RMVar_ID_70219 Human_SNP_ID_668347778 m1A Human chr19 + 49447441 49447441 49447441 GCGGATGTTCTGCTGCGAGATGGAGCCCATGAATGGCCGGTTCTTCATCATGCGCCATTCTGAGG GCGGATGTTCTGCTGCGAGATGGAGCCCATGATTGGCCGGTTCTTCATCATGCGCCATTCTGAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49447390..49447503 26863196 MeRIP-seq:(Medium) rs756040837 Functional Loss SNV dbSNP153 33..33 33 - - - 70220 RMVar_ID_70220 Human_SNP_ID_668347894 m1A Human chr19 + 49447776 49447775 49447776 AGCCAGCCCCTCCTCTCCTAGGGGTGTTCCCCAAACCGCTCCTGGCTCCACTCTTTCCCGAGGGC AGCCAGCCCCTCCTCTCCTAGGGGTGTTCCCC_AACCGCTCCTGGCTCCACTCTTTCCCGAGGGC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49447774..49447943 26863196 MeRIP-seq:(Medium) rs1339935560 Functional Loss DEL dbSNP153 33..33 33 - - - 70221 RMVar_ID_70221 Human_SNP_ID_668348122 m1A Human chr19 - 49448435 49448435 49448435 AGCCAGTAATGGAGAGTGACTGAAAGAAATTCAGTGGGCCGAGGTTGCTAGAAGAATGAGGTCTT AGCCAGTAATGGAGAGTGACTGAAAGAAATTCTGTGGGCCGAGGTTGCTAGAAGAATGAGGTCTT T A PIH1D1 Ensembl:ENSG00000104872 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49448432..49448610 26863196 MeRIP-seq:(Medium) rs1323017072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13495171,Human_RBP_ID_18737416,Human_RBP_ID_23804446 RMVar_hsa_circ_96360,RMVar_hsa_circ_195834,RMVar_hsa_circ_74117 70222 RMVar_ID_70222 Human_SNP_ID_668349105 m1A Human chr19 - 49451550 49451550 49451550 CCAGGGCCATGGCGAACCCGAAGCTGCTGGGAATGGGGCTAAGCGAGGCGGAGGCGATCGGTGCT CCAGGGCCATGGCGAACCCGAAGCTGCTGGGACTGGGGCTAAGCGAGGCGGAGGCGATCGGTGCT T G PIH1D1 Ensembl:ENSG00000104872 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49451476..49451550 32194978 MeRIP-seq:(Medium) rs2293012 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22977799,Human_RBP_ID_26474267 Human_Splice_Rec_2030111,Human_Splice_Rec_2030208,Human_Splice_Rec_2030209,Human_Splice_Rec_2030241,Human_Splice_Rec_2030255,Human_Splice_Rec_2030266,Human_Splice_Rec_2030267,Human_Splice_Rec_2030278,Human_Splice_Rec_2030289,Human_Splice_Rec_2030297,Human_Splice_Rec_2030301,Human_Splice_Rec_2030306,Human_Splice_Rec_2030307 GWAS_ID_8418,GWAS_ID_8419,GWAS_ID_8420,GWAS_ID_8421,GWAS_ID_8422,GWAS_ID_8423,GWAS_ID_8424,GWAS_ID_8425,GWAS_ID_8426,GWAS_ID_8427,GWAS_ID_8428,GWAS_ID_8429,GWAS_ID_8430,GWAS_ID_8431,GWAS_ID_8432,GWAS_ID_8433,GWAS_ID_8434,GWAS_ID_8435 RMVar_hsa_circ_96360,RMVar_hsa_circ_195834,RMVar_hsa_circ_113228,RMVar_hsa_circ_195841 70223 RMVar_ID_70223 Human_SNP_ID_668349749 m1A Human chr19 + 49453341 49453341 49453341 GCGGAAAGCGTTCGGGGTAGGCGATGGCTGCGACGCGTGCAGGGCCCCGCGCCCGCGAGATCTTC GCGGAAAGCGTTCGGGGTAGGCGATGGCTGCGGCGCGTGCAGGGCCCCGCGCCCGCGAGATCTTC A G ALDH16A1 Ensembl:ENSG00000161618 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49453293..49453465 26863196 MeRIP-seq:(Medium) rs1434595426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772738,Human_RBP_ID_4558665,Human_RBP_ID_18737423 Human_Splice_Rec_2030313,Human_Splice_Rec_2030339,Human_Splice_Rec_2030371,Human_Splice_Rec_2030399,Human_Splice_Rec_2030429,Human_Splice_Rec_2030457 70224 RMVar_ID_70224 Human_SNP_ID_668349823 m1A Human chr19 - 49453423 49453423 49453423 CGCAGCGAGCAGCGCCGGCCGGGCAGACTCTCACCAGTGCGCATGCGTGGCTCTCCGGCACCGGT CGCAGCGAGCAGCGCCGGCCGGGCAGACTCTCGCCAGTGCGCATGCGTGGCTCTCCGGCACCGGT T C PIH1D1 Ensembl:ENSG00000104872 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49453389..49453477 26863196 MeRIP-seq:(Medium) rs1162898984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2030207,Human_Splice_Rec_2030265,Human_Splice_Rec_2030305 70225 RMVar_ID_70225 Human_SNP_ID_668351299 m1A Human chr19 + 49458542 49458542 49458542 TGCTTGGGCCACTATGTGAATGGGAAGTGGTTAAAGCCTGAACACAGAAATTCAGTGCCTTGCCA TGCTTGGGCCACTATGTGAATGGGAAGTGGTTGAAGCCTGAACACAGAAATTCAGTGCCTTGCCA A G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49453318..49462610 32194978 MeRIP-seq:(Medium) rs1212287009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2030340,Human_Splice_Rec_2030341,Human_Splice_Rec_2030372,Human_Splice_Rec_2030373,Human_Splice_Rec_2030400,Human_Splice_Rec_2030401,Human_Splice_Rec_2030458,Human_Splice_Rec_2030459 Human_miRNA_ID_2892376 RMVar_hsa_circ_195844,RMVar_hsa_circ_319103 70226 RMVar_ID_70226 Human_SNP_ID_668352155 m1A Human chr19 + 49461327 49461112 49461328 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT __________________________________CTGGACTCCTGGGTCTGAGGGAGGAGGGGCT TCTGGACTCCTGAGTCTGAGGGAGGAGGGGCTGGAGTCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGGTCTGGATTCCTGGGTCTGAGGGAGGAGGGGCTGGGGTCTGGACTCCTGGGTGTGAGGGAGGAGGGGCTGGGGTCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGAC T ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49461276..49461469;chr19:49461276..49461442 26863196 MeRIP-seq:(Medium) rs1568650482 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5321832,Human_RBP_ID_8199027,Human_RBP_ID_8233518,Human_RBP_ID_8942486 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70227 RMVar_ID_70227 Human_SNP_ID_668352191 m1A Human chr19 + 49461327 49461162 49461328 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT __________________________________CTGGACTCCTGGGTCTGAGGGAGGAGGGGCT TCTGAGGGAGGAGGGGCTGGGGTCTGGATTCCTGGGTCTGAGGGAGGAGGGGCTGGGGTCTGGACTCCTGGGTGTGAGGGAGGAGGGGCTGGGGTCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGAC T ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49461276..49461469;chr19:49461276..49461442 26863196 MeRIP-seq:(Medium) rs1568650565 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5321832,Human_RBP_ID_8199027,Human_RBP_ID_8233518,Human_RBP_ID_8942486 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70228 RMVar_ID_70228 Human_SNP_ID_668352262 m1A Human chr19 + 49461291 49461290 49461291 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGG_CCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GA G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:49461284..49461427;chr19:49461276..49461451 26863196 MeRIP-seq:(Medium) rs373121562 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_263338,Human_RBP_ID_826988,Human_RBP_ID_3583940,Human_RBP_ID_3955386,Human_RBP_ID_5321832,Human_RBP_ID_8100778,Human_RBP_ID_8196785,Human_RBP_ID_8233206,Human_RBP_ID_8942486,Human_RBP_ID_9426363,Human_RBP_ID_17190782,Human_RBP_ID_21979375 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70229 RMVar_ID_70229 Human_SNP_ID_668352265 m1A Human chr19 + 49461291 49461291 49461291 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT A G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:49461284..49461427;chr19:49461276..49461451 26863196 MeRIP-seq:(Medium) rs559858125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263338,Human_RBP_ID_826988,Human_RBP_ID_3583940,Human_RBP_ID_3955386,Human_RBP_ID_5321832,Human_RBP_ID_8100778,Human_RBP_ID_8196785,Human_RBP_ID_8233206,Human_RBP_ID_8942486,Human_RBP_ID_9426363,Human_RBP_ID_17190782,Human_RBP_ID_21979375 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70230 RMVar_ID_70230 Human_SNP_ID_668352279 m1A Human chr19 + 49461327 49461326 49461327 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGG_CCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GA G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49461276..49461469;chr19:49461276..49461442 26863196 MeRIP-seq:(Medium) rs374952578 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5321832,Human_RBP_ID_8199027,Human_RBP_ID_8233518,Human_RBP_ID_8942486 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70231 RMVar_ID_70231 Human_SNP_ID_668352281 m1A Human chr19 + 49461327 49461327 49461327 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT A G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49461276..49461469;chr19:49461276..49461442 26863196 MeRIP-seq:(Medium) rs1462549904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5321832,Human_RBP_ID_8199027,Human_RBP_ID_8233518,Human_RBP_ID_8942486 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70232 RMVar_ID_70232 Human_SNP_ID_668352785 m1A Human chr19 - 49461957 49461954 49461957 AGTCTACGTCCGCCGTGTCCGTCAGCAGCAGCAGCGACTCCGTCCCCAGCGCCAGGCCCAGCTCC AGTCTACGTCCGCCGTGTCCGTCAGCAGCAGC___GACTCCGTCCCCAGCGCCAGGCCCAGCTCC CGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:49461563..49462025;chr19:49461823..49462051 26863196 MeRIP-seq:(Medium) rs753339031 Functional Loss DEL dbSNP153 33..35 33 - - - 70233 RMVar_ID_70233 Human_SNP_ID_668352788 m1A Human chr19 - 49461960 49461960 49461960 CCGAGTCTACGTCCGCCGTGTCCGTCAGCAGCAGCAGCGACTCCGTCCCCAGCGCCAGGCCCAGC CCGAGTCTACGTCCGCCGTGTCCGTCAGCAGCCGCAGCGACTCCGTCCCCAGCGCCAGGCCCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49461826..49462068 26863196 MeRIP-seq:(Medium) rs1262540765 Functional Loss SNV dbSNP153 33..33 33 - - - 70234 RMVar_ID_70234 Human_SNP_ID_668354064 m1A Human chr19 - 49464667 49464667 49464667 TTCAGGTTCTTGGAGAGGCAGGACAGCCGGGCAGGGGTCCCTGAGGGCCGCAGATACTCATACAG TTCAGGTTCTTGGAGAGGCAGGACAGCCGGGCTGGGGTCCCTGAGGGCCGCAGATACTCATACAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49462709..49465771 32194978 MeRIP-seq:(Medium) rs146453544 Functional Loss SNV dbSNP153 33..33 33 - - - 70235 RMVar_ID_70235 Human_SNP_ID_668354065 m1A Human chr19 - 49464667 49464667 49464667 TTCAGGTTCTTGGAGAGGCAGGACAGCCGGGCAGGGGTCCCTGAGGGCCGCAGATACTCATACAG TTCAGGTTCTTGGAGAGGCAGGACAGCCGGGCGGGGGTCCCTGAGGGCCGCAGATACTCATACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49462709..49465771 32194978 MeRIP-seq:(Medium) rs146453544 Functional Loss SNV dbSNP153 33..33 33 - - - 70236 RMVar_ID_70236 Human_SNP_ID_668354618 m1A Human chr19 + 49466183 49466183 49466183 GAAGTCTACCCTGGCCTCGAGGCTGGAGAGGCAGGGAGCGGAGCTCAAGGCTGCGGAGGCGGAGG GAAGTCTACCCTGGCCTCGAGGCTGGAGAGGCCGGGAGCGGAGCTCAAGGCTGCGGAGGCGGAGG A C ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49466133..49466335 26863196 MeRIP-seq:(Medium) rs1453510105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23211345 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70237 RMVar_ID_70237 Human_SNP_ID_668355346 m1A Human chr19 + 49468454 49468454 49468454 GCTGGGTGTGCTGGCTGTGGTGTGTCCGGACGAGTGGCCCCTGCTTGCCTTCGTGTCCCTGCTGG GCTGGGTGTGCTGGCTGTGGTGTGTCCGGACGGGTGGCCCCTGCTTGCCTTCGTGTCCCTGCTGG A G ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49468404..49469051 32194978 MeRIP-seq:(Medium) rs773685135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293858,Human_RBP_ID_13495312,Human_RBP_ID_23804464,Human_RBP_ID_26770079 Human_Splice_Rec_2030334,Human_Splice_Rec_2030366,Human_Splice_Rec_2030396,Human_Splice_Rec_2030424,Human_Splice_Rec_2030452,Human_Splice_Rec_2030468 Human_miRNA_ID_2933045 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 70238 RMVar_ID_70238 Human_SNP_ID_668357421 m1A Human chr19 - 49475267 49475209 49475268 TTGGCTCTGTCCACCTTCCCTCTCCTCTGTCCATCTCCCCCCTTTTCTGTCCATCTCCCCCTCCT TTGGCTCTGTCCACCTTCCCTCTCCTCTGTC__________________________________ AGACAGAGGAGGGGGGAGATGGACAGAGGAGGGGGAGATGGACAGAAAAGGGGGGAGATG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49475257..49475398 26863196 MeRIP-seq:(Medium) rs1568665272 Functional Loss DEL dbSNP153 32..65 33 - - - 70239 RMVar_ID_70239 Human_SNP_ID_668357447 m1A Human chr19 + 49475256 49475256 49475256 GAGATGGACAGAGGAGGGGGAGATGGACAGAAAAGGGGGGAGATGGACAGAGGAGAGGGAAGGTG GAGATGGACAGAGGAGGGGGAGATGGACAGAAGAGGGGGGAGATGGACAGAGGAGAGGGAAGGTG A G AC010619.3,FLT3LG,AC010619.2 Ensembl:ENSG00000273189,Ensembl:ENSG00000090554,Ensembl:ENSG00000269469 lincRNA,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49475250..49475417 26863196 MeRIP-seq:(Medium) rs965129081 Functional Loss SNV dbSNP153 33..33 33 - - - 70240 RMVar_ID_70240 Human_SNP_ID_668357450 m1A Human chr19 - 49475267 49475267 49475267 TTGGCTCTGTCCACCTTCCCTCTCCTCTGTCCATCTCCCCCCTTTTCTGTCCATCTCCCCCTCCT TTGGCTCTGTCCACCTTCCCTCTCCTCTGTCCGTCTCCCCCCTTTTCTGTCCATCTCCCCCTCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49475257..49475398 26863196 MeRIP-seq:(Medium) rs1342488890 Functional Loss SNV dbSNP153 33..33 33 - - - 70241 RMVar_ID_70241 Human_SNP_ID_668357451 m1A Human chr19 - 49475267 49475267 49475267 TTGGCTCTGTCCACCTTCCCTCTCCTCTGTCCATCTCCCCCCTTTTCTGTCCATCTCCCCCTCCT TTGGCTCTGTCCACCTTCCCTCTCCTCTGTCCCTCTCCCCCCTTTTCTGTCCATCTCCCCCTCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49475257..49475398 26863196 MeRIP-seq:(Medium) rs1342488890 Functional Loss SNV dbSNP153 33..33 33 - - - 70242 RMVar_ID_70242 Human_SNP_ID_668359128 m1A Human chr19 + 49480354 49480354 49480354 GGAGTCCCCGGCCCCTGGAGGCCACAGCCCCGACAGCCCCGCAGCCCCCTCTGCTCCTCCTACTG GGAGTCCCCGGCCCCTGGAGGCCACAGCCCCGTCAGCCCCGCAGCCCCCTCTGCTCCTCCTACTG A T AC010619.3,FLT3LG,AC010619.2 Ensembl:ENSG00000273189,Ensembl:ENSG00000090554,Ensembl:ENSG00000269469 lincRNA,Protein coding,Protein coding exon,3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49478936..49480569 26863196 MeRIP-seq:(Medium) rs1380527971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589615 Human_Splice_Rec_2030496,Human_Splice_Rec_2030512,Human_Splice_Rec_2030528,Human_Splice_Rec_2030544,Human_Splice_Rec_2030560,Human_Splice_Rec_2030576,Human_Splice_Rec_2030590,Human_Splice_Rec_2030610,Human_Splice_Rec_2030628,Human_Splice_Rec_2030644 RMVar_hsa_circ_1968,RMVar_hsa_circ_357665,RMVar_hsa_circ_275311 70243 RMVar_ID_70243 Human_SNP_ID_668361370 m1A Human chr19 + 49487643 49487643 49487643 TTCCAAGCGGCTGCCGAAGATGGCGGAGGTGCAGGTATGGGCTCCGCGCGGGCCGGGGCGGCAAG TTCCAAGCGGCTGCCGAAGATGGCGGAGGTGCGGGTATGGGCTCCGCGCGGGCCGGGGCGGCAAG A G RPL13A Ensembl:ENSG00000142541 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49487631..49487758 26863196 MeRIP-seq:(Medium) rs981754447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240408,Human_RBP_ID_771810,Human_RBP_ID_826295,Human_RBP_ID_915165,Human_RBP_ID_4559811,Human_RBP_ID_13495419,Human_RBP_ID_18192402,Human_RBP_ID_18421672,Human_RBP_ID_27277017 Human_Splice_Rec_2030649,Human_Splice_Rec_2030661,Human_Splice_Rec_2030675,Human_Splice_Rec_2030683,Human_Splice_Rec_2030697,Human_Splice_Rec_2030701,Human_Splice_Rec_2030715,Human_Splice_Rec_2030727,Human_Splice_Rec_2030733,Human_Splice_Rec_2030747 Human_miRNA_ID_2751256 RMVar_hsa_circ_81809,RMVar_hsa_circ_121194,RMVar_hsa_circ_370369,RMVar_hsa_circ_117654,RMVar_hsa_circ_195849,RMVar_hsa_circ_195851,RMVar_hsa_circ_195852,RMVar_hsa_circ_195850 70244 RMVar_ID_70244 Human_SNP_ID_668362429 m1A Human chr19 - 49490201 49490201 49490201 GCCTAGAGGGAGGGAAAGGCTTAGCAGGGCCGAGCCGCCTGAGGGTCCCACCACTGCCTATGCAG GCCTAGAGGGAGGGAAAGGCTTAGCAGGGCCGGGCCGCCTGAGGGTCCCACCACTGCCTATGCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49490197..49490300 26863196 MeRIP-seq:(Medium) rs1568687234 Functional Loss SNV dbSNP153 33..33 33 - - - 70245 RMVar_ID_70245 Human_SNP_ID_668362560 m1A Human chr19 + 49490532 49490532 49490532 GCGGATGAACACCAACCCTTCCCGAGGCCCCTACCACTTCCGGGCCCCCAGCCGCATCTTCTGGC GCGGATGAACACCAACCCTTCCCGAGGCCCCTGCCACTTCCGGGCCCCCAGCCGCATCTTCTGGC A G RPL13A Ensembl:ENSG00000142541 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49490482..49490642;chr19:49490210..49490550;chr19:49490472..49490631 26863196 MeRIP-seq:(Medium) rs11539122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525338,Human_RBP_ID_8492008,Human_RBP_ID_9089245,Human_RBP_ID_13495541,Human_RBP_ID_17929320,Human_RBP_ID_18192411,Human_RBP_ID_18737449,Human_RBP_ID_26816185,Human_RBP_ID_27470283 Human_Splice_Rec_2030652,Human_Splice_Rec_2030653,Human_Splice_Rec_2030666,Human_Splice_Rec_2030667,Human_Splice_Rec_2030680,Human_Splice_Rec_2030681,Human_Splice_Rec_2030688,Human_Splice_Rec_2030689,Human_Splice_Rec_2030706,Human_Splice_Rec_2030707,Human_Splice_Rec_2030719,Human_Splice_Rec_2030730,Human_Splice_Rec_2030731,Human_Splice_Rec_2030738,Human_Splice_Rec_2030739,Human_Splice_Rec_2030752,Human_Splice_Rec_2030753,Human_Splice_Rec_2030765 Human_miRNA_ID_2686335 RMVar_hsa_circ_4010,RMVar_hsa_circ_93538,RMVar_hsa_circ_121194,RMVar_hsa_circ_370369,RMVar_hsa_circ_117654,RMVar_hsa_circ_195851,RMVar_hsa_circ_195852,RMVar_hsa_circ_195850,RMVar_hsa_circ_110400,RMVar_hsa_circ_195853,RMVar_hsa_circ_76627,RMVar_hsa_circ_88559,RMVar_hsa_circ_195855,RMVar_hsa_circ_195856,RMVar_hsa_circ_195854,RMVar_hsa_circ_117816,RMVar_hsa_circ_119078,RMVar_hsa_circ_39674,RMVar_hsa_circ_102790,RMVar_hsa_circ_124311,RMVar_hsa_circ_195857,RMVar_hsa_circ_195858,RMVar_hsa_circ_125278,RMVar_hsa_circ_370155,RMVar_hsa_circ_114135,RMVar_hsa_circ_195860,RMVar_hsa_circ_195862,RMVar_hsa_circ_195863,RMVar_hsa_circ_195861,RMVar_hsa_circ_195859 70246 RMVar_ID_70246 Human_SNP_ID_668362579 m1A Human chr19 - 49490561 49490561 49490561 CCCCACGCTCTGCTCACCTCGCACGGTCCGCCAGAAGATGCGGCTGGGGGCCCGGAAGTGGTAGG CCCCACGCTCTGCTCACCTCGCACGGTCCGCCGGAAGATGCGGCTGGGGGCCCGGAAGTGGTAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49490514..49490777 26863196 MeRIP-seq:(Medium) rs767311936 Functional Loss SNV dbSNP153 33..33 33 - - - 70247 RMVar_ID_70247 Human_SNP_ID_668362697 m1A Human chr19 + 49490751 49490747 49490751 GGGGTGGGTGGGCATCCTTATGAGGCCCTCTGACTGGGCCTGCTATCTGTCACCCAACAGGTATG GGGGTGGGTGGGCATCCTTATGAGGCCCT____CTGGGCCTGCTATCTGTCACCCAACAGGTATG TCTGA T RPL13A Ensembl:ENSG00000142541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49490748..49490834 26863196 MeRIP-seq:(Medium) rs1240239054 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_121194,RMVar_hsa_circ_370369,RMVar_hsa_circ_195851,RMVar_hsa_circ_195852,RMVar_hsa_circ_110400,RMVar_hsa_circ_76627,RMVar_hsa_circ_88559,RMVar_hsa_circ_195855,RMVar_hsa_circ_195856,RMVar_hsa_circ_195854,RMVar_hsa_circ_117816,RMVar_hsa_circ_119078,RMVar_hsa_circ_39674,RMVar_hsa_circ_102790,RMVar_hsa_circ_124311,RMVar_hsa_circ_195857,RMVar_hsa_circ_195858,RMVar_hsa_circ_125278,RMVar_hsa_circ_114135,RMVar_hsa_circ_195860,RMVar_hsa_circ_195862,RMVar_hsa_circ_195861,RMVar_hsa_circ_195859 70248 RMVar_ID_70248 Human_SNP_ID_668365200 m1A Human chr19 + 49496455 49496455 49496455 GCTGCCCCTTTCTTTTTTTCAGGCGGCCGGGAAGATGGCGGACATTCAGGTGCGGACTCGGGGTT GCTGCCCCTTTCTTTTTTTCAGGCGGCCGGGAGGATGGCGGACATTCAGGTGCGGACTCGGGGTT A G RPS11 Ensembl:ENSG00000142534 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49496401..49496563 26863196 MeRIP-seq:(Medium) rs372959624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240405,Human_RBP_ID_525366,Human_RBP_ID_771805,Human_RBP_ID_825143,Human_RBP_ID_912694,Human_RBP_ID_1017525,Human_RBP_ID_4542181,Human_RBP_ID_5191733,Human_RBP_ID_5443349,Human_RBP_ID_6778842,Human_RBP_ID_13495603,Human_RBP_ID_17656314,Human_RBP_ID_17929340,Human_RBP_ID_22071685,Human_RBP_ID_22503452,Human_RBP_ID_24420199 Human_Splice_Rec_2030777,Human_Splice_Rec_2030783,Human_Splice_Rec_2030787,Human_Splice_Rec_2030793,Human_Splice_Rec_2030799,Human_Splice_Rec_2030807,Human_Splice_Rec_2030815,Human_Splice_Rec_2030819,Human_Splice_Rec_2030827 RMVar_hsa_circ_111118,RMVar_hsa_circ_112495,RMVar_hsa_circ_195871,RMVar_hsa_circ_195872 70249 RMVar_ID_70249 Human_SNP_ID_668365518 m1A Human chr19 + 49497273 49497273 49497273 GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGAAGCTCCCGCGGTACTACAAGAACATCGGTCTGG GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGAGGCTCCCGCGGTACTACAAGAACATCGGTCTGG A G RPS11 Ensembl:ENSG00000142534 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49496426..49497375 26863410 MeRIP-seq:(Medium) rs778586777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525368,Human_RBP_ID_1133000,Human_RBP_ID_1569681,Human_RBP_ID_1890935,Human_RBP_ID_3575098,Human_RBP_ID_4571896,Human_RBP_ID_5194270,Human_RBP_ID_5585851,Human_RBP_ID_8256284,Human_RBP_ID_8492049,Human_RBP_ID_9089257,Human_RBP_ID_9381288,Human_RBP_ID_13495622,Human_RBP_ID_17385140,Human_RBP_ID_17502490,Human_RBP_ID_18737484,Human_RBP_ID_22811767,Human_RBP_ID_23131668,Human_RBP_ID_26816188,Human_RBP_ID_26993554 Human_Splice_Rec_2030778,Human_Splice_Rec_2030779,Human_Splice_Rec_2030784,Human_Splice_Rec_2030788,Human_Splice_Rec_2030794,Human_Splice_Rec_2030795,Human_Splice_Rec_2030801,Human_Splice_Rec_2030808,Human_Splice_Rec_2030809,Human_Splice_Rec_2030816,Human_Splice_Rec_2030820,Human_Splice_Rec_2030821,Human_Splice_Rec_2030828,Human_Splice_Rec_2030829 RMVar_hsa_circ_111118,RMVar_hsa_circ_112495,RMVar_hsa_circ_195871,RMVar_hsa_circ_195872,RMVar_hsa_circ_195873,RMVar_hsa_circ_89688 70250 RMVar_ID_70250 Human_SNP_ID_668365519 m1A Human chr19 + 49497273 49497273 49497273 GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGAAGCTCCCGCGGTACTACAAGAACATCGGTCTGG GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGATGCTCCCGCGGTACTACAAGAACATCGGTCTGG A T RPS11 Ensembl:ENSG00000142534 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49496426..49497375 26863410 MeRIP-seq:(Medium) rs778586777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525368,Human_RBP_ID_1133000,Human_RBP_ID_1569681,Human_RBP_ID_1890935,Human_RBP_ID_3575098,Human_RBP_ID_4571896,Human_RBP_ID_5194270,Human_RBP_ID_5585851,Human_RBP_ID_8256284,Human_RBP_ID_8492049,Human_RBP_ID_9089257,Human_RBP_ID_9381288,Human_RBP_ID_13495622,Human_RBP_ID_17385140,Human_RBP_ID_17502490,Human_RBP_ID_18737484,Human_RBP_ID_22811767,Human_RBP_ID_23131668,Human_RBP_ID_26816188,Human_RBP_ID_26993554 Human_Splice_Rec_2030778,Human_Splice_Rec_2030779,Human_Splice_Rec_2030784,Human_Splice_Rec_2030788,Human_Splice_Rec_2030794,Human_Splice_Rec_2030795,Human_Splice_Rec_2030801,Human_Splice_Rec_2030808,Human_Splice_Rec_2030809,Human_Splice_Rec_2030816,Human_Splice_Rec_2030820,Human_Splice_Rec_2030821,Human_Splice_Rec_2030828,Human_Splice_Rec_2030829 RMVar_hsa_circ_111118,RMVar_hsa_circ_112495,RMVar_hsa_circ_195871,RMVar_hsa_circ_195872,RMVar_hsa_circ_195873,RMVar_hsa_circ_89688 70251 RMVar_ID_70251 Human_SNP_ID_668365540 m1A Human chr19 - 49497327 49497327 49497327 AGGTTCCCCTTCTTTCTTCTGAGGTTCCCCGCACCTCCTTGGGTGTCTTGAAGCCCAGACCGATG AGGTTCCCCTTCTTTCTTCTGAGGTTCCCCGCGCCTCCTTGGGTGTCTTGAAGCCCAGACCGATG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49497276..49497350 26863196 MeRIP-seq:(Medium) rs879095417 Functional Loss SNV dbSNP153 33..33 33 - - - 70252 RMVar_ID_70252 Human_SNP_ID_668365598 m1A Human chr19 - 49497434 49497432 49497435 AGAGCCAGGGGCGTGGCCTCAGGGAAGCAACTACAATTCCCAGCAGCCCCAGAAGCCACTTAGAT AGAGCCAGGGGCGTGGCCTCAGGGAAGCAAC___AATTCCCAGCAGCCCCAGAAGCCACTTAGAT TGTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49497431..49497629 26863196 MeRIP-seq:(Medium) rs1354400593 Functional Loss DEL dbSNP153 32..34 33 - - - 70253 RMVar_ID_70253 Human_SNP_ID_668365640 m1A Human chr19 - 49497504 49497504 49497504 TAGGTGCCCTCAATAGCCTGAAAGGATAGGAAAGATAAAGGAGTGAGCCTTGGGCGGGCGGTTCC TAGGTGCCCTCAATAGCCTGAAAGGATAGGAACGATAAAGGAGTGAGCCTTGGGCGGGCGGTTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49497501..49497525 26863196 MeRIP-seq:(Medium) rs762318979 Functional Loss SNV dbSNP153 33..33 33 - - - 70254 RMVar_ID_70254 Human_SNP_ID_668365863 m1A Human chr19 + 49498018 49498018 49498018 AGTACAACCGCTTCGAGAAGCGCCACAAGAACATGTCTGTACACCTGTCCCCCTGCTTCAGGTGA AGTACAACCGCTTCGAGAAGCGCCACAAGAACGTGTCTGTACACCTGTCCCCCTGCTTCAGGTGA A G RPS11 Ensembl:ENSG00000142534 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:49497853..49498089 26863196 MeRIP-seq:(Medium) rs747738184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525382,Human_RBP_ID_912698,Human_RBP_ID_1095025,Human_RBP_ID_1569689,Human_RBP_ID_1890943,Human_RBP_ID_4571910,Human_RBP_ID_5194272,Human_RBP_ID_8492060,Human_RBP_ID_13495640,Human_RBP_ID_17270247,Human_RBP_ID_17387008,Human_RBP_ID_17501180,Human_RBP_ID_18737493,Human_RBP_ID_19090667,Human_RBP_ID_26469717,Human_RBP_ID_26993567,Human_RBP_ID_27470332 Human_Splice_Rec_2030781,Human_Splice_Rec_2030785,Human_Splice_Rec_2030791,Human_Splice_Rec_2030805,Human_Splice_Rec_2030813,Human_Splice_Rec_2030825,Human_Splice_Rec_2030833 Human_miRNA_ID_2891263 RMVar_hsa_circ_111118,RMVar_hsa_circ_112495,RMVar_hsa_circ_86678,RMVar_hsa_circ_195871,RMVar_hsa_circ_195872,RMVar_hsa_circ_195873,RMVar_hsa_circ_89688,RMVar_hsa_circ_345108,RMVar_hsa_circ_195875,RMVar_hsa_circ_80072,RMVar_hsa_circ_90333,RMVar_hsa_circ_195874,RMVar_hsa_circ_195876 70255 RMVar_ID_70255 Human_SNP_ID_668365869 m1A Human chr19 - 49498033 49498033 49498033 GATGGGCCACTGCGCTCACCTGAAGCAGGGGGACAGGTGTACAGACATGTTCTTGTGGCGCTTCT GATGGGCCACTGCGCTCACCTGAAGCAGGGGGCCAGGTGTACAGACATGTTCTTGTGGCGCTTCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:49497901..49498082;chr19:49497976..49498082 32194978 MeRIP-seq:(Medium) rs1260629200 Functional Loss SNV dbSNP153 33..33 33 - - - 70256 RMVar_ID_70256 Human_SNP_ID_668370324 m1A Human chr19 + 49512713 49512713 49512713 GGGTCTCCAGTCACGGGAGCCAGGAGCCGGCCAGGGCCGCAGGCAGGAAGGGAGCGAGGCTGAAG GGGTCTCCAGTCACGGGAGCCAGGAGCCGGCCTGGGCCGCAGGCAGGAAGGGAGCGAGGCTGAAG A T FCGRT Ensembl:ENSG00000104870 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49512666..49513219 32194978 MeRIP-seq:(Medium) rs1269733789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557652,Human_RBP_ID_18420967 Human_Splice_Rec_2030843,Human_Splice_Rec_2030847,Human_Splice_Rec_2030859 70257 RMVar_ID_70257 Human_SNP_ID_668374681 m1A Human chr19 + 49526062 49526062 49526062 GGAGACGACACCGGGGTCCTCCTGCCCACCCCAGGGGAGGCCCAGGATGCTGATTTGAAGGATGT GGAGACGACACCGGGGTCCTCCTGCCCACCCCGGGGGAGGCCCAGGATGCTGATTTGAAGGATGT A G FCGRT Ensembl:ENSG00000104870 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49525337..49526283 32194978 MeRIP-seq:(Medium) rs762854571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525411,Human_RBP_ID_911787,Human_RBP_ID_5117576,Human_RBP_ID_17657293,Human_RBP_ID_22764245,Human_RBP_ID_23804566 Human_Splice_Rec_2030858,Human_Splice_Rec_2030874,Human_Splice_Rec_2030884,Human_Splice_Rec_2030900,Human_Splice_Rec_2030912,Human_Splice_Rec_2030920,Human_Splice_Rec_2030952 70258 RMVar_ID_70258 Human_SNP_ID_668374715 m1A Human chr19 + 49526135 49526135 49526135 TTCCAGCCACCGCCTGACCATCCGCCATTCCGACTGCTAAAAGCGAATGTAGTCAGGCCCCTTTC TTCCAGCCACCGCCTGACCATCCGCCATTCCGGCTGCTAAAAGCGAATGTAGTCAGGCCCCTTTC A G FCGRT Ensembl:ENSG00000104870 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49526084..49526283 32194978 MeRIP-seq:(Medium) rs201766783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525412,Human_RBP_ID_5117577,Human_RBP_ID_17656324,Human_RBP_ID_26816213 70259 RMVar_ID_70259 Human_SNP_ID_668379827 m1A Human chr19 + 49542625 49542625 49542625 GTGGGTGCAGACGGAGAGGCAGCAGTTCCGGGACTTCCGGGATCTGAACAAGGATGGGCACCTGG GTGGGTGCAGACGGAGAGGCAGCAGTTCCGGGGCTTCCGGGATCTGAACAAGGATGGGCACCTGG A G RCN3 Ensembl:ENSG00000142552 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49542534..49542825;chr19:49539156..49542730;chr19:49534258..49543202;chr19:49542575..49542670 26863196 MeRIP-seq:(Medium) rs767971433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909734,Human_RBP_ID_5117048 Human_Splice_Rec_2030962,Human_Splice_Rec_2030979 RMVar_hsa_circ_120759,RMVar_hsa_circ_60692,RMVar_hsa_circ_16143,RMVar_hsa_circ_195878 70260 RMVar_ID_70260 Human_SNP_ID_668380083 m1A Human chr19 + 49543251 49543251 49543251 GCGCACCTGCCACAGCCTCAGAGGCCCGCACAATGACCGGAGGAGGGGCCGCTGTGGTCTGGCCC GCGCACCTGCCACAGCCTCAGAGGCCCGCACAGTGACCGGAGGAGGGGCCGCTGTGGTCTGGCCC A G RCN3 Ensembl:ENSG00000142552 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49543201..49543475 32194978 MeRIP-seq:(Medium) rs745480457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2077287,Human_miRNA_ID_2939107 RMVar_hsa_circ_120759,RMVar_hsa_circ_195878 70261 RMVar_ID_70261 Human_SNP_ID_668380143 m1A Human chr19 - 49543474 49543474 49543474 TTGGGGCGGTTCTTAGAGCTGAGCTTGGGGCCAAGGGTCCCTGGGTCTGGGCTGGGAGACTCAGT TTGGGGCGGTTCTTAGAGCTGAGCTTGGGGCCGAGGGTCCCTGGGTCTGGGCTGGGAGACTCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49543425..49543531 26863196 MeRIP-seq:(Medium) rs939601880 Functional Loss SNV dbSNP153 33..33 33 - - - 70262 RMVar_ID_70262 Human_SNP_ID_668384735 m1A Human chr19 - 49557245 49557245 49557245 GATGCTCAGCCCACTTTCCCCGACGCAGGCCTACGAGAAGCAGCGGGGCACCCGGCGCGAGGAGC GATGCTCAGCCCACTTTCCCCGACGCAGGCCTGCGAGAAGCAGCGGGGCACCCGGCGCGAGGAGC T C NOSIP Ensembl:ENSG00000142546 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49557101..49557291 26863196 MeRIP-seq:(Medium) rs1367188779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826515,Human_RBP_ID_4542290,Human_RBP_ID_9381300,Human_RBP_ID_19094002,Human_RBP_ID_22070436,Human_RBP_ID_26338141,Human_RBP_ID_27815588 Human_Splice_Rec_2030988,Human_Splice_Rec_2031002,Human_Splice_Rec_2031030,Human_Splice_Rec_2031062,Human_Splice_Rec_2031076,Human_Splice_Rec_2031086,Human_Splice_Rec_2031098,Human_Splice_Rec_2031120 RMVar_hsa_circ_195879,RMVar_hsa_circ_79136,RMVar_hsa_circ_109332,RMVar_hsa_circ_195880 70263 RMVar_ID_70263 Human_SNP_ID_668385179 m1A Human chr19 - 49558878 49558878 49558878 CCCGGCAGATGAAGGTGATGGGGATGGGGAGGAGGCGGCACACGGAGGCAGGAGCTTTTGAGTCT CCCGGCAGATGAAGGTGATGGGGATGGGGAGGCGGCGGCACACGGAGGCAGGAGCTTTTGAGTCT T G NOSIP Ensembl:ENSG00000142546 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49558876..49559272;chr19:49558876..49559000 26863196 MeRIP-seq:(Medium) rs773691874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955394,Human_RBP_ID_19090673 Human_Splice_Rec_2031096,Human_Splice_Rec_2031108 RMVar_hsa_circ_195879,RMVar_hsa_circ_79136,RMVar_hsa_circ_109332,RMVar_hsa_circ_195880 70264 RMVar_ID_70264 Human_SNP_ID_668385200 m1A Human chr19 - 49558947 49558947 49558947 GCCCAGATGGCTACCTGTATGAGCGTGAGGCCATCCTGGAGTACATTCTGCACCAGAAGAAGGAG GCCCAGATGGCTACCTGTATGAGCGTGAGGCCGTCCTGGAGTACATTCTGCACCAGAAGAAGGAG T C NOSIP Ensembl:ENSG00000142546 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:49558876..49559000;chr19:49558876..49559272 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1477134927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569704,Human_RBP_ID_1890954,Human_RBP_ID_3955394,Human_RBP_ID_9381302,Human_RBP_ID_22449606,Human_RBP_ID_26338142 Human_Splice_Rec_2030986,Human_Splice_Rec_2030987,Human_Splice_Rec_2031000,Human_Splice_Rec_2031001,Human_Splice_Rec_2031014,Human_Splice_Rec_2031028,Human_Splice_Rec_2031029,Human_Splice_Rec_2031044,Human_Splice_Rec_2031045,Human_Splice_Rec_2031058,Human_Splice_Rec_2031059,Human_Splice_Rec_2031074,Human_Splice_Rec_2031075,Human_Splice_Rec_2031084,Human_Splice_Rec_2031085,Human_Splice_Rec_2031096,Human_Splice_Rec_2031097,Human_Splice_Rec_2031108,Human_Splice_Rec_2031109,Human_Splice_Rec_2031118,Human_Splice_Rec_2031119,Human_Splice_Rec_2031122,Human_Splice_Rec_2031123,Human_Splice_Rec_2031126,Human_Splice_Rec_2031127,Human_Splice_Rec_2031132 RMVar_hsa_circ_195879,RMVar_hsa_circ_79136,RMVar_hsa_circ_109332,RMVar_hsa_circ_195880 70265 RMVar_ID_70265 Human_SNP_ID_668388368 m1A Human chr19 + 49570685 49570685 49570685 CCTCCGACTTCCCCCTGACCCCCAAGCTTCTCAGTGAACGTCCAACACCTGTTGCCTCCCCTCAC CCTCCGACTTCCCCCTGACCCCCAAGCTTCTCGGTGAACGTCCAACACCTGTTGCCTCCCCTCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49570683..49570790 26863196 MeRIP-seq:(Medium) rs571833455 Functional Loss SNV dbSNP153 33..33 33 - - - 70266 RMVar_ID_70266 Human_SNP_ID_668390803 m1A Human chr19 - 49580387 49580387 49580387 ATTCCCGATTCCCTGTCAATCATTATTAATACAGCTGTCCGGGCGCCCCAAGTTTGAAGCTGAAC ATTCCCGATTCCCTGTCAATCATTATTAATACCGCTGTCCGGGCGCCCCAAGTTTGAAGCTGAAC T G NOSIP Ensembl:ENSG00000142546 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49580385..49580550 26863196 MeRIP-seq:(Medium) rs1273515333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5372035,Human_RBP_ID_13495874 RMVar_hsa_circ_23847,RMVar_hsa_circ_79470,RMVar_hsa_circ_195886 70267 RMVar_ID_70267 Human_SNP_ID_668393990 m1A Human chr19 + 49591240 49591240 49591240 AGATGGCTGCACCGTGAGCGCAGAGGAGGAGGAGGCGGCGGCGGCGGCGGCGAGAGAGCGAGCAC AGATGGCTGCACCGTGAGCGCAGAGGAGGAGGCGGCGGCGGCGGCGGCGGCGAGAGAGCGAGCAC A C PRR12 Ensembl:ENSG00000126464 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:49591201..49591445;chr19:49591238..49591445 26863196 MeRIP-seq:(Medium) rs1341468898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4542312 70268 RMVar_ID_70268 Human_SNP_ID_668394003 m1A Human chr19 + 49591264 49591256 49591264 GGAGGAGGAGGCGGCGGCGGCGGCGGCGAGAGAGCGAGCACCCAGCGCCTGCACCCACCCCGGGG GGAGGAGGAGGCGGCGGCGGCGGCG________GCGAGCACCCAGCGCCTGCACCCACCCCGGGG GGCGAGAGA G PRR12 Ensembl:ENSG00000126464 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49591215..49591425 26863196 MeRIP-seq:(Medium) rs939903760 Functional Loss DEL dbSNP153 26..33 33 - - - 70269 RMVar_ID_70269 Human_SNP_ID_668394007 m1A Human chr19 + 49591264 49591264 49591264 GGAGGAGGAGGCGGCGGCGGCGGCGGCGAGAGAGCGAGCACCCAGCGCCTGCACCCACCCCGGGG GGAGGAGGAGGCGGCGGCGGCGGCGGCGAGAGCGCGAGCACCCAGCGCCTGCACCCACCCCGGGG A C PRR12 Ensembl:ENSG00000126464 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49591215..49591425 26863196 MeRIP-seq:(Medium) rs112369566 Functional Loss SNV dbSNP153 33..33 33 - - - 70270 RMVar_ID_70270 Human_SNP_ID_668394210 m1A Human chr19 + 49591641 49591633 49591641 TCCCTCCCTCCCTCCCCCTCCCCCCAATTTCCACCGCGGCCAATTCATGGACAGGAACTACCCCA TCCCTCCCTCCCTCCCCCTCCCCCC________CCGCGGCCAATTCATGGACAGGAACTACCCCA CAATTTCCA C PRR12 Ensembl:ENSG00000126464 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:49591597..49591773;chr19:49591504..49591725 26863196 MeRIP-seq:(Medium) rs753264728 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_22067980 Human_Splice_Rec_2031183 70271 RMVar_ID_70271 Human_SNP_ID_668394218 m1A Human chr19 + 49591641 49591641 49591641 TCCCTCCCTCCCTCCCCCTCCCCCCAATTTCCACCGCGGCCAATTCATGGACAGGAACTACCCCA TCCCTCCCTCCCTCCCCCTCCCCCCAATTTCCCCCGCGGCCAATTCATGGACAGGAACTACCCCA A C PRR12 Ensembl:ENSG00000126464 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:49591597..49591773;chr19:49591504..49591725 26863196 MeRIP-seq:(Medium) rs568196363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22067980 Human_Splice_Rec_2031183 70272 RMVar_ID_70272 Human_SNP_ID_668395563 m1A Human chr19 + 49595043 49595043 49595043 CCTTACCGCCCTGGCCCCCCAGACCCACCACCACCTCCTCGCCACCTCCCAACTCAGTTCAACCT CCTTACCGCCCTGGCCCCCCAGACCCACCACCGCCTCCTCGCCACCTCCCAACTCAGTTCAACCT A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49594993..49595190 26863196 MeRIP-seq:(Medium) rs1311260696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2089251,Human_miRNA_ID_2090123 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70273 RMVar_ID_70273 Human_SNP_ID_668396425 m1A Human chr19 - 49596740 49596740 49596740 AGGGACTGGGGGCATGGCTGAGGACCGAGGGGAGCAGCTGGGGGGGAGGCGGAGGCAGCACCAGT AGGGACTGGGGGCATGGCTGAGGACCGAGGGGTGCAGCTGGGGGGGAGGCGGAGGCAGCACCAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49596693..49596996 26863196 MeRIP-seq:(Medium) rs1426875771 Functional Loss SNV dbSNP153 33..33 33 - - - 70274 RMVar_ID_70274 Human_SNP_ID_668396672 m1A Human chr19 - 49597132 49597132 49597132 CTCCTCGTCTTGGAGCAAGGAGTCAGGGAAGCAGATGGAGGTGAGCGGCACGAAACGCGGCGCCT CTCCTCGTCTTGGAGCAAGGAGTCAGGGAAGCCGATGGAGGTGAGCGGCACGAAACGCGGCGCCT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49597020..49597520 32194978 MeRIP-seq:(Medium) rs1424305536 Functional Loss SNV dbSNP153 33..33 33 - - - 70275 RMVar_ID_70275 Human_SNP_ID_668396890 m1A Human chr19 + 49597455 49597455 49597455 ATCCAGAGTGGCCCCCACCAGGCGGCGCCACCACCCCCGCCTCCGCCACCGCCGCCTCCCGCGCC ATCCAGAGTGGCCCCCACCAGGCGGCGCCACCCCCCCCGCCTCCGCCACCGCCGCCTCCCGCGCC A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49597405..49597550 26863196 MeRIP-seq:(Medium) rs943019426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525430 Human_miRNA_ID_2147442,Human_miRNA_ID_2988868,Human_miRNA_ID_3022570 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70276 RMVar_ID_70276 Human_SNP_ID_668396891 m1A Human chr19 + 49597455 49597455 49597455 ATCCAGAGTGGCCCCCACCAGGCGGCGCCACCACCCCCGCCTCCGCCACCGCCGCCTCCCGCGCC ATCCAGAGTGGCCCCCACCAGGCGGCGCCACCGCCCCCGCCTCCGCCACCGCCGCCTCCCGCGCC A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49597405..49597550 26863196 MeRIP-seq:(Medium) rs943019426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525430 Human_miRNA_ID_2147442,Human_miRNA_ID_2988868,Human_miRNA_ID_3022570 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70277 RMVar_ID_70277 Human_SNP_ID_668396899 m1A Human chr19 + 49597470 49597461 49597470 CACCAGGCGGCGCCACCACCCCCGCCTCCGCCACCGCCGCCTCCCGCGCCGGCCTCCGAACCCAA CACCAGGCGGCGCCACCACCCCCG_________CCGCCGCCTCCCGCGCCGGCCTCCGAACCCAA GCCTCCGCCA G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr19:49597426..49597625;chr19:49597425..49597564 26863196 MeRIP-seq:(Medium) rs1568423508 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_525430 Human_miRNA_ID_2250382 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70278 RMVar_ID_70278 Human_SNP_ID_668397005 m1A Human chr19 + 49597685 49597685 49597685 CAAGGCCGATGTTCCCGCCGACATCCGCCTCAACCCCCGGCGCTTGCCTGACCTGGTCTCCAGCT CAAGGCCGATGTTCCCGCCGACATCCGCCTCAGCCCCCGGCGCTTGCCTGACCTGGTCTCCAGCT A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49597651..49597700 26863196 MeRIP-seq:(Medium) rs78322972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27470382 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70279 RMVar_ID_70279 Human_SNP_ID_668397045 m1A Human chr19 + 49597757 49597757 49597757 CCGTCCGGCCCTCTCGCCACTGGGGGACATCGACTTCTGCCCACCCAACCCAGGACCCGATGGCC CCGTCCGGCCCTCTCGCCACTGGGGGACATCGCCTTCTGCCCACCCAACCCAGGACCCGATGGCC A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49597401..49597800 26863196 MeRIP-seq:(Medium) rs1164891025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240083,Human_RBP_ID_8836311,Human_RBP_ID_17929385 Human_miRNA_ID_2874265,Human_miRNA_ID_2982226 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 70280 RMVar_ID_70280 Human_SNP_ID_668397710 m1A Human chr19 + 49599477 49599477 49599477 CTTCTTGGACTTCCTCAAGTCAGGCAAGCGCCACCCACCACTCTACCAGGCGGGCCTGACGCCTC CTTCTTGGACTTCCTCAAGTCAGGCAAGCGCCCCCCACCACTCTACCAGGCGGGCCTGACGCCTC A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49599427..49599528 32194978 MeRIP-seq:(Medium) rs1396966125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146026,Human_RBP_ID_5527293 RMVar_hsa_circ_276777,RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_323762,RMVar_hsa_circ_195888 70281 RMVar_ID_70281 Human_SNP_ID_668398511 m1A Human chr19 - 49601660 49601660 49601660 GGTGGTGGTGGAGGCGAGGGCATGGCTGGTGGAGGTGGCGGCGGCAGCGGCGGTGGCGGTGGTGA GGTGGTGGTGGAGGCGAGGGCATGGCTGGTGGTGGTGGCGGCGGCAGCGGCGGTGGCGGTGGTGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr19:49601454..49601775;chr19:49601465..49601781 26863410,26863196 MeRIP-seq:(Medium) rs1419484796 Functional Loss SNV dbSNP153 33..33 33 - - - 70282 RMVar_ID_70282 Human_SNP_ID_668398513 m1A Human chr19 + 49601663 49601663 49601663 CCACCGCCACCGCCGCTGCCGCCGCCACCTCCACCAGCCATGCCCTCGCCTCCACCACCACCCCC CCACCGCCACCGCCGCTGCCGCCGCCACCTCCCCCAGCCATGCCCTCGCCTCCACCACCACCCCC A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49601576..49601775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_27470389 Human_miRNA_ID_2052820,Human_miRNA_ID_2494003,Human_miRNA_ID_2696286 RMVar_hsa_circ_276777,RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_195888,RMVar_hsa_circ_368010 70283 RMVar_ID_70283 Human_SNP_ID_668402609 m1A Human chr19 + 49615318 49615318 49615318 GGAGACTCAGAAGGAGACAGAGACCCAGAGAAAAAGAGGGACAGAGATGGGGGAGGACAAAGATC GGAGACTCAGAAGGAGACAGAGACCCAGAGAAGAAGAGGGACAGAGATGGGGGAGGACAAAGATC A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49615251..49615413 26863196 MeRIP-seq:(Medium) rs1332568248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_68727,RMVar_hsa_circ_295359,RMVar_hsa_circ_195889 70284 RMVar_ID_70284 Human_SNP_ID_668402799 m1A Human chr19 + 49615844 49615844 49615844 CAGCACCACCTCCCAAGCCTGAGACCCCTGAAAAGACGACATCTGAGAAGCCCCCAGAGCAGACT CAGCACCACCTCCCAAGCCTGAGACCCCTGAAGAGACGACATCTGAGAAGCCCCCAGAGCAGACT A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49615793..49616218 26863196 MeRIP-seq:(Medium) rs1224910862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2031198,Human_Splice_Rec_2031218 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_68727,RMVar_hsa_circ_295359,RMVar_hsa_circ_195889,RMVar_hsa_circ_345556 70285 RMVar_ID_70285 Human_SNP_ID_668402814 m1A Human chr19 - 49615879 49615879 49615879 TCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGGCTTCTCAGATGTCGT TCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCGGGAGTCTGCTCTGGGGGCTTCTCAGATGTCGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49615749..49616095 26863196 MeRIP-seq:(Medium) rs778558246 Functional Loss SNV dbSNP153 33..33 33 - - - 70286 RMVar_ID_70286 Human_SNP_ID_668402821 m1A Human chr19 - 49615894 49615894 49615894 AGGAGGGAGGGCTTCTCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGG AGGAGGGAGGGCTTCTCGGGGGCAGGGGGCTCTGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49615761..49616005 26863196 MeRIP-seq:(Medium) rs768432276 Functional Loss SNV dbSNP153 33..33 33 - - - 70287 RMVar_ID_70287 Human_SNP_ID_668402822 m1A Human chr19 - 49615894 49615894 49615894 AGGAGGGAGGGCTTCTCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGG AGGAGGGAGGGCTTCTCGGGGGCAGGGGGCTCGGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:49615761..49616005 26863196 MeRIP-seq:(Medium) rs768432276 Functional Loss SNV dbSNP153 33..33 33 - - - 70288 RMVar_ID_70288 Human_SNP_ID_668402860 m1A Human chr19 + 49615974 49615974 49615974 GGAAAAGGAGAAGGAGAAGGTGACACGTGGAGAGCGGCCATTGCGGGGTGAGCGGGCCACCAGCG GGAAAAGGAGAAGGAGAAGGTGACACGTGGAGGGCGGCCATTGCGGGGTGAGCGGGCCACCAGCG A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49615790..49616113 26863196 MeRIP-seq:(Medium) rs1254474129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381307 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_68727,RMVar_hsa_circ_295359,RMVar_hsa_circ_195889,RMVar_hsa_circ_345556 70289 RMVar_ID_70289 Human_SNP_ID_668402923 m1A Human chr19 + 49616091 49616091 49616091 CCGGCTGCCCAAAGCCCGGCCTACCAAGGTGAAGGCTGAACCGCCCCCTAAGAAGAGGAAGAAAT CCGGCTGCCCAAAGCCCGGCCTACCAAGGTGAGGGCTGAACCGCCCCCTAAGAAGAGGAAGAAAT A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49615854..49616105 32194978 MeRIP-seq:(Medium) rs1190605258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_871284,Human_miRNA_ID_2387475,Human_miRNA_ID_2388947,Human_miRNA_ID_2400095,Human_miRNA_ID_3031157 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_68727,RMVar_hsa_circ_295359,RMVar_hsa_circ_195889,RMVar_hsa_circ_345556 70290 RMVar_ID_70290 Human_SNP_ID_668404230 m1A Human chr19 + 49620384 49620384 49620384 AGCGGGCAGTACCTGGGCGTCTGCTCAAAACCAGGGCGATGCGGGAGATGTACCGGAGCTACGTG AGCGGGCAGTACCTGGGCGTCTGCTCAAAACCGGGGCGATGCGGGAGATGTACCGGAGCTACGTG A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49616204..49621584 32194978 MeRIP-seq:(Medium) rs773809173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527104,Human_RBP_ID_6778964,Human_RBP_ID_8836329 Human_Splice_Rec_2031200,Human_Splice_Rec_2031201,Human_Splice_Rec_2031220,Human_Splice_Rec_2031221,Human_Splice_Rec_2031229 RMVar_hsa_circ_68727,RMVar_hsa_circ_44878,RMVar_hsa_circ_345556 70291 RMVar_ID_70291 Human_SNP_ID_668404259 m1A Human chr19 - 49620479 49620479 49620479 AGCCCCCCCCCCTCCTCCCCAGGCCTCAGCTCACCATGCGTGTCCTCCAGGGCCTGGATCATGTC AGCCCCCCCCCCTCCTCCCCAGGCCTCAGCTCGCCATGCGTGTCCTCCAGGGCCTGGATCATGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49620474..49620698 26863196 MeRIP-seq:(Medium) rs112186538 Functional Loss SNV dbSNP153 33..33 33 - - - 70292 RMVar_ID_70292 Human_SNP_ID_668404261 m1A Human chr19 + 49620486 49620486 49620486 TCCAGGCCCTGGAGGACACGCATGGTGAGCTGAGGCCTGGGGAGGAGGGGGGGGGGCTGACTCGG TCCAGGCCCTGGAGGACACGCATGGTGAGCTGGGGCCTGGGGAGGAGGGGGGGGGGCTGACTCGG A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49620484..49620710 26863196 MeRIP-seq:(Medium) rs1481169713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44878 70293 RMVar_ID_70293 Human_SNP_ID_668404265 m1A Human chr19 + 49620496 49620493 49620496 GGAGGACACGCATGGTGAGCTGAGGCCTGGGGAGGAGGGGGGGGGGCTGACTCGGTCTGAGGGAG GGAGGACACGCATGGTGAGCTGAGGCCTGG___GGAGGGGGGGGGGCTGACTCGGTCTGAGGGAG GGGA G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49620490..49620690 26863196 MeRIP-seq:(Medium) rs752355262 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_44878 70294 RMVar_ID_70294 Human_SNP_ID_668404266 m1A Human chr19 + 49620496 49620495 49620496 GGAGGACACGCATGGTGAGCTGAGGCCTGGGGAGGAGGGGGGGGGGCTGACTCGGTCTGAGGGAG GGAGGACACGCATGGTGAGCTGAGGCCTGGGG_GGAGGGGGGGGGGCTGACTCGGTCTGAGGGAG GA G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49620490..49620690 26863196 MeRIP-seq:(Medium) rs1466613235 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_44878 70295 RMVar_ID_70295 Human_SNP_ID_668404520 m1A Human chr19 + 49621210 49621210 49621210 GCTGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGGGTCTGGACTCTTGGGTCAGAGA GCTGGGGCCTGGACTCCTGGGTCTGAGGGAGGGGGGGCTGGGGGTCTGGACTCTTGGGTCAGAGA A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49621209..49621522 26863196 MeRIP-seq:(Medium) rs1368967652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44878 70296 RMVar_ID_70296 Human_SNP_ID_668405609 m1A Human chr19 - 49624172 49624172 49624172 ACCACCTATCCTATCCCAGAATTCTCAGCCCCATCGTAACCACCTACCCCAGAATTCTCGGTCCC ACCACCTATCCTATCCCAGAATTCTCAGCCCCGTCGTAACCACCTACCCCAGAATTCTCGGTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49623929..49624637 26863196 MeRIP-seq:(Medium) rs1286991784 Functional Loss SNV dbSNP153 33..33 33 - - - 70297 RMVar_ID_70297 Human_SNP_ID_668405639 m1A Human chr19 + 49624258 49624258 49624258 GGGGTAGGTGGTTAGGATGGGGCCGAGCATTCAGGGATAGGTGGTTAGGATGGGGCTGAGAATTC GGGGTAGGTGGTTAGGATGGGGCCGAGCATTCTGGGATAGGTGGTTAGGATGGGGCTGAGAATTC A T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49623970..49624621 26863196 MeRIP-seq:(Medium) rs1264776323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290998 70298 RMVar_ID_70298 Human_SNP_ID_668409106 m1A Human chr19 + 49635353 49635353 49635353 GGGGAGGGGAGTTATATACAGCAGTGACCCGGAGCCCCTCACCCCCACCAGGCTTAGGTGGGGAC GGGGAGGGGAGTTATATACAGCAGTGACCCGGCGCCCCTCACCCCCACCAGGCTTAGGTGGGGAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49635346..49635508 26863196 MeRIP-seq:(Medium) rs1379997366 Functional Loss SNV dbSNP153 33..33 33 - - - 70299 RMVar_ID_70299 Human_SNP_ID_668409170 m1A Human chr19 - 49635572 49635572 49635572 GCGGGGGCTGCCCCTGCGTCCTCCTGTAGCCCAGGCAAGAGAGAAGCAACCACCACAAGCTCTCG GCGGGGGCTGCCCCTGCGTCCTCCTGTAGCCCGGGCAAGAGAGAAGCAACCACCACAAGCTCTCG T C RRAS Ensembl:ENSG00000126458 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49635347..49635755 26863196 MeRIP-seq:(Medium) rs199675852 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_137905 Human_Splice_Rec_2031242 RMVar_hsa_circ_107260,RMVar_hsa_circ_124806,RMVar_hsa_circ_123998,RMVar_hsa_circ_195890,RMVar_hsa_circ_99034,RMVar_hsa_circ_100121,RMVar_hsa_circ_195892,RMVar_hsa_circ_195893,RMVar_hsa_circ_195894,RMVar_hsa_circ_195891 70300 RMVar_ID_70300 Human_SNP_ID_668409671 m1A Human chr19 + 49636950 49636950 49636950 TGTCCAGGACTGCAGAGACAGGGAGAGGGGCCATCGTGGGGACCAGGCTCCCCGCAGTCACCCCC TGTCCAGGACTGCAGAGACAGGGAGAGGGGCCGTCGTGGGGACCAGGCTCCCCGCAGTCACCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49636946..49637026 26863196 MeRIP-seq:(Medium) rs750473587 Functional Loss SNV dbSNP153 33..33 33 - - - 70301 RMVar_ID_70301 Human_SNP_ID_668409716 m1A Human chr19 - 49637056 49637056 49637056 TACACGAAGATCTGCAGTGTGGATGGCATCCCAGCCCGGCTGGACAGTGAGGGCGGCAAGGATGG TACACGAAGATCTGCAGTGTGGATGGCATCCCGGCCCGGCTGGACAGTGAGGGCGGCAAGGATGG T C RRAS Ensembl:ENSG00000126458 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49637047..49640008 32194978 MeRIP-seq:(Medium) rs1400974619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2031234,Human_Splice_Rec_2031235,Human_Splice_Rec_2031244 Human_miRNA_ID_2975079,Human_miRNA_ID_3008274 RMVar_hsa_circ_107260,RMVar_hsa_circ_195890,RMVar_hsa_circ_100121,RMVar_hsa_circ_195891 70302 RMVar_ID_70302 Human_SNP_ID_668409746 m1A Human chr19 - 49637126 49637126 49637126 AGTAACTATCCTCTCCCCACCCCGCCAGTCCTACTTCGTGTCTGACTACGACCCCACTATTGAGG AGTAACTATCCTCTCCCCACCCCGCCAGTCCTTCTTCGTGTCTGACTACGACCCCACTATTGAGG T A RRAS Ensembl:ENSG00000126458 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49637076..49637150 26863196 MeRIP-seq:(Medium) rs908791453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2031234,Human_Splice_Rec_2031235,Human_Splice_Rec_2031244 Clinvar_Rec_285 RMVar_hsa_circ_107260,RMVar_hsa_circ_195890,RMVar_hsa_circ_100121,RMVar_hsa_circ_195891 70303 RMVar_ID_70303 Human_SNP_ID_668411229 m1A Human chr19 - 49642244 49642244 49642244 AGCCCCGCGGCCCGGACTGCCGCCGCCATCTTACCCCGCCGCTCGGGCTGCGGCTCCGGCCCCGG AGCCCCGCGGCCCGGACTGCCGCCGCCATCTTCCCCCGCCGCTCGGGCTGCGGCTCCGGCCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49642228..49642402;chr19:49642232..49642390;chr19:49642231..49642401;chr19:49642237..49642391 26863196 MeRIP-seq:(Medium) rs1017851393 Functional Loss SNV dbSNP153 33..33 33 - - - 70304 RMVar_ID_70304 Human_SNP_ID_668412252 m1A Human chr19 - 49646222 49646222 49646222 CTTCCTCCCTGATACCCGTGAGCCAGGCCCCCAGCCCCCTCTTCTTACTCACAGTAGCCGTGTCA CTTCCTCCCTGATACCCGTGAGCCAGGCCCCCCGCCCCCTCTTCTTACTCACAGTAGCCGTGTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49646219..49646323 26863196 MeRIP-seq:(Medium) rs1248011540 Functional Loss SNV dbSNP153 33..33 33 - - - 70305 RMVar_ID_70305 Human_SNP_ID_668413545 m1A Human chr19 - 49650975 49650975 49650975 AGGGGAGGAAGATGAGGGAGAAGGGGAAGGGGAGGAGGATGCAGAGGAGGGGGCAGGGGGTGGGG AGGGGAGGAAGATGAGGGAGAAGGGGAAGGGGGGGAGGATGCAGAGGAGGGGGCAGGGGGTGGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:49650886..49650974 26863410 MeRIP-seq:(Medium) rs1328484150 Functional Loss SNV dbSNP153 33..33 33 - - - 70306 RMVar_ID_70306 Human_SNP_ID_668413556 m1A Human chr19 - 49651002 49651002 49651002 AGGGGGCGGTGGGGGTGGGGGAGGGGAAGGGGAGGAAGATGAGGGAGAAGGGGAAGGGGAGGAGG AGGGGGCGGTGGGGGTGGGGGAGGGGAAGGGGGGGAAGATGAGGGAGAAGGGGAAGGGGAGGAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49650851..49651050 26863196 MeRIP-seq:(Medium) rs1282886168 Functional Loss SNV dbSNP153 33..33 33 - - - 70307 RMVar_ID_70307 Human_SNP_ID_668413691 m1A Human chr19 + 49651253 49651253 49651253 GAAGAGGAAGAGGAAGACGAGGAGGAGGAGGAAGGCCTGTCCCAGAGCATCAGCCGCATCTCGGA GAAGAGGAAGAGGAAGACGAGGAGGAGGAGGAGGGCCTGTCCCAGAGCATCAGCCGCATCTCGGA A G SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:49650885..49651775;chr19:49651076..49652233 26863196 MeRIP-seq:(Medium) rs764217789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908851,Human_RBP_ID_3955399,Human_RBP_ID_5146027,Human_RBP_ID_5527105,Human_RBP_ID_6779101,Human_RBP_ID_9381309,Human_RBP_ID_22072062,Human_RBP_ID_22663041,Human_RBP_ID_22742580,Human_RBP_ID_26338145,Human_RBP_ID_26769861,Human_RBP_ID_27816630 Human_miRNA_ID_1966684,Human_miRNA_ID_2362142,Human_miRNA_ID_2425696,Human_miRNA_ID_2435365,Human_miRNA_ID_2908700,Human_miRNA_ID_3027539 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70308 RMVar_ID_70308 Human_SNP_ID_668413920 m1A Human chr19 + 49651647 49651647 49651647 TCTTCCGCCCCGGCGGCCGGGCCGCCCGGCCTACACCGGCCGCCTCGGCCACCCCCACGGCCCAG TCTTCCGCCCCGGCGGCCGGGCCGCCCGGCCTCCACCGGCCGCCTCGGCCACCCCCACGGCCCAG A C SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49651322..49652225 26863410 MeRIP-seq:(Medium) rs7251334 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70309 RMVar_ID_70309 Human_SNP_ID_668414068 m1A Human chr19 + 49651947 49651947 49651947 CCGCTGCTGGTCCGCCCACGCGCAAGAAGTCCAGGCGGGAACGCAAGCGCAGCGGCGAGGCCAAG CCGCTGCTGGTCCGCCCACGCGCAAGAAGTCCCGGCGGGAACGCAAGCGCAGCGGCGAGGCCAAG A C SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49651901..49652049 26863196 MeRIP-seq:(Medium) rs1043965095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293861 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70310 RMVar_ID_70310 Human_SNP_ID_668414357 m1A Human chr19 + 49652406 49652406 49652406 CCCCGGCGCCCGCCCCGCCGCCCTCTGGCTCCACCTCGTGTGGTGACCGCGACAGCCGCCGCCGG CCCCGGCGCCCGCCCCGCCGCCCTCTGGCTCCCCCTCGTGTGGTGACCGCGACAGCCGCCGCCGG A C SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49652321..49652422 26863410 MeRIP-seq:(Medium) rs763895281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569743,Human_RBP_ID_9292600,Human_RBP_ID_17929459,Human_RBP_ID_22811794 Human_miRNA_ID_2172548 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70311 RMVar_ID_70311 Human_SNP_ID_668414358 m1A Human chr19 + 49652406 49652406 49652406 CCCCGGCGCCCGCCCCGCCGCCCTCTGGCTCCACCTCGTGTGGTGACCGCGACAGCCGCCGCCGG CCCCGGCGCCCGCCCCGCCGCCCTCTGGCTCCTCCTCGTGTGGTGACCGCGACAGCCGCCGCCGG A T SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49652321..49652422 26863410 MeRIP-seq:(Medium) rs763895281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569743,Human_RBP_ID_9292600,Human_RBP_ID_17929459,Human_RBP_ID_22811794 Human_miRNA_ID_2172548 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70312 RMVar_ID_70312 Human_SNP_ID_668414986 m1A Human chr19 + 49653481 49653476 49653482 GGCGGAGGAGGAGGAGGAGGAAGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAGGAGCAGCAGC GGCGGAGGAGGAGGAGGAGGAAGAAGAA______GAGGAAGAGGAAGAGGAGGAGGAGCAGCAGC AGAGGAG A SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49652872..49653650 26863196 MeRIP-seq:(Medium) rs750992003 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_9347017,Human_RBP_ID_22720508,Human_RBP_ID_26338147 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70313 RMVar_ID_70313 Human_SNP_ID_668414987 m1A Human chr19 + 49653481 49653476 49653482 GGCGGAGGAGGAGGAGGAGGAAGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAGGAGCAGCAGC GGCGGAGGAGGAGGAGGAGGAAGAAGAAGAG___GAGGAAGAGGAAGAGGAGGAGGAGCAGCAGC AGAGGAG AGAG SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49652872..49653650 26863196 MeRIP-seq:(Medium) rs750992003 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9347017,Human_RBP_ID_22720508,Human_RBP_ID_26338147 RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 70314 RMVar_ID_70314 Human_SNP_ID_668416968 m1A Human chr19 + 49659689 49659689 49659689 CCCAGGGCCCTGGAAATCCATGCCCTCCACCAAGTCCTGCAGGTAGGCCTTGTACTGGTCGGAGG CCCAGGGCCCTGGAAATCCATGCCCTCCACCAGGTCCTGCAGGTAGGCCTTGTACTGGTCGGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49659639..49659717 26863196 MeRIP-seq:(Medium) rs757832899 Functional Loss SNV dbSNP153 33..33 33 - - - 70315 RMVar_ID_70315 Human_SNP_ID_668416993 m1A Human chr19 + 49659783 49659783 49659783 TGCAGGTCCACAGTATTCTCCAGGGAGGAGGCACCCCCTACCCGGGCCATTTCTACCAAGGCCCT TGCAGGTCCACAGTATTCTCCAGGGAGGAGGCGCCCCCTACCCGGGCCATTTCTACCAAGGCCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49659618..49660847 32194978 MeRIP-seq:(Medium) rs1341395213 Functional Loss SNV dbSNP153 33..33 33 - - - 70316 RMVar_ID_70316 Human_SNP_ID_668417897 m1A Human chr19 - 49662025 49662019 49662025 ATACTGGGCAGTGAGCGAGGAGCTGCTCCCCAACAGCGGGCATGGGCCTGATGGCGAGGTCCCCA ATACTGGGCAGTGAGCGAGGAGCTGCTCCCCA______GGCATGGGCCTGATGGCGAGGTCCCCA CCGCTGT C IRF3 Ensembl:ENSG00000126456 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49661974..49662095 26863196 MeRIP-seq:(Medium) rs1397361919 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_17935074,Human_RBP_ID_18995293 Human_Splice_Rec_2031305,Human_Splice_Rec_2031317,Human_Splice_Rec_2031329,Human_Splice_Rec_2031349,Human_Splice_Rec_2031363,Human_Splice_Rec_2031377,Human_Splice_Rec_2031417,Human_Splice_Rec_2031445,Human_Splice_Rec_2031459,Human_Splice_Rec_2031475 RMVar_hsa_circ_44287 70317 RMVar_ID_70317 Human_SNP_ID_668418135 m1A Human chr19 + 49662527 49662527 49662527 GTCCAAGCTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTC GTCCAAGCTGGGGCTCCGCAGGGGCTGAGGGCGGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49662477..49662579 26863196 MeRIP-seq:(Medium) rs897364474 Functional Loss SNV dbSNP153 33..33 33 - - - 70318 RMVar_ID_70318 Human_SNP_ID_668418137 m1A Human chr19 + 49662534 49662533 49662535 CTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTCCCGGATC CTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTC__GGGCTACAGCCAGGCTTGGGGGTCCCGGATC CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr19:49662484..49662581;chr19:49662485..49663206 26863196,32194978 MeRIP-seq:(Medium) rs1486451862 Functional Loss DEL dbSNP153 33..34 33 - - - 70319 RMVar_ID_70319 Human_SNP_ID_668418138 m1A Human chr19 + 49662534 49662534 49662534 CTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCAGGGGCTACAGCCAGGCTTGGGGGTCCCGGATC CTGGGGCTCCGCAGGGGCTGAGGGCAGGGCTCGGGGGCTACAGCCAGGCTTGGGGGTCCCGGATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr19:49662484..49662581;chr19:49662485..49663206 26863196,32194978 MeRIP-seq:(Medium) rs1024647445 Functional Loss SNV dbSNP153 33..33 33 - - - 70320 RMVar_ID_70320 Human_SNP_ID_668418411 m1A Human chr19 - 49663401 49663401 49663401 GCCCTCAACCGCAAAGAAGGGTTGCGTTTAGCAGAGGACCGGAGCAAGGACCCTCACGACCCACA GCCCTCAACCGCAAAGAAGGGTTGCGTTTAGCTGAGGACCGGAGCAAGGACCCTCACGACCCACA T A IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49663376..49663400 32194978 MeRIP-seq:(Medium) rs1568461826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955405,Human_RBP_ID_17929479,Human_RBP_ID_18998498,Human_RBP_ID_22977509 Human_Splice_Rec_2031299,Human_Splice_Rec_2031311,Human_Splice_Rec_2031323,Human_Splice_Rec_2031333,Human_Splice_Rec_2031343,Human_Splice_Rec_2031357,Human_Splice_Rec_2031371,Human_Splice_Rec_2031385,Human_Splice_Rec_2031399,Human_Splice_Rec_2031411,Human_Splice_Rec_2031423,Human_Splice_Rec_2031453,Human_Splice_Rec_2031467,Human_Splice_Rec_2031481,Human_Splice_Rec_2031499,Human_Splice_Rec_2031507,Human_Splice_Rec_2031517,Human_Splice_Rec_2031525,Human_Splice_Rec_2031539,Human_Splice_Rec_2031549,Human_Splice_Rec_2031553 RMVar_hsa_circ_44287 70321 RMVar_ID_70321 Human_SNP_ID_668418625 m1A Human chr19 + 49664197 49664197 49664197 CCAAAAACCTTTTCTTTCTAAGCCAGGCTTCCAAGTCCAACTTGGTGTCTAATCCCGTGCACCAC CCAAAAACCTTTTCTTTCTAAGCCAGGCTTCCGAGTCCAACTTGGTGTCTAATCCCGTGCACCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49664193..49664317 26863196 MeRIP-seq:(Medium) rs1385526055 Functional Loss SNV dbSNP153 33..33 33 - - - 70322 RMVar_ID_70322 Human_SNP_ID_668418860 m1A Human chr19 - 49664751 49664751 49664751 GGCAACTGGAGGGCGTGGCCTGGGTGAACAAGAGCCGCACGCGCTTCCGCATCCCTTGGAAGCAC GGCAACTGGAGGGCGTGGCCTGGGTGAACAAGCGCCGCACGCGCTTCCGCATCCCTTGGAAGCAC T G IRF3 Ensembl:ENSG00000126456 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49664174..49664760 26863196 MeRIP-seq:(Medium) rs1234152111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569763,Human_RBP_ID_22977805,Human_RBP_ID_27470488 Human_Splice_Rec_2031309,Human_Splice_Rec_2031321,Human_Splice_Rec_2031340,Human_Splice_Rec_2031341,Human_Splice_Rec_2031354,Human_Splice_Rec_2031355,Human_Splice_Rec_2031368,Human_Splice_Rec_2031369,Human_Splice_Rec_2031383,Human_Splice_Rec_2031396,Human_Splice_Rec_2031397,Human_Splice_Rec_2031464,Human_Splice_Rec_2031465,Human_Splice_Rec_2031479,Human_Splice_Rec_2031514,Human_Splice_Rec_2031515,Human_Splice_Rec_2031530,Human_Splice_Rec_2031531,Human_Splice_Rec_2031536,Human_Splice_Rec_2031537,Human_Splice_Rec_2031543,Human_Splice_Rec_2031556,Human_Splice_Rec_2031557 70323 RMVar_ID_70323 Human_SNP_ID_668419214 m1A Human chr19 - 49665675 49665673 49665675 TCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCCCCGAC TCGAGTTTGAGAGCTACCCGGAGCTCCAAGAC__GGGTGGGTTCCAGCTGCCCGCACGCCCCGAC CCT C IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49665624..49665733 32194978 MeRIP-seq:(Medium) rs1245121989 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1017565 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 70324 RMVar_ID_70324 Human_SNP_ID_668419218 m1A Human chr19 - 49665675 49665675 49665675 TCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCCCCGAC TCGAGTTTGAGAGCTACCCGGAGCTCCAAGACGGGGGTGGGTTCCAGCTGCCCGCACGCCCCGAC T C IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49665624..49665733 32194978 MeRIP-seq:(Medium) rs563734774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017565 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 70325 RMVar_ID_70325 Human_SNP_ID_668419219 m1A Human chr19 - 49665677 49665677 49665677 CCTCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCCCCG CCTCGAGTTTGAGAGCTACCCGGAGCTCCAAGTCAGGGGTGGGTTCCAGCTGCCCGCACGCCCCG T A IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49665449..49665704 26863196 MeRIP-seq:(Medium) rs1294013801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017565,Human_RBP_ID_4542787 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 70326 RMVar_ID_70326 Human_SNP_ID_668419220 m1A Human chr19 - 49665677 49665677 49665677 CCTCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCCCCG CCTCGAGTTTGAGAGCTACCCGGAGCTCCAAGGCAGGGGTGGGTTCCAGCTGCCCGCACGCCCCG T C IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49665449..49665704 26863196 MeRIP-seq:(Medium) rs1294013801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017565,Human_RBP_ID_4542787 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 70327 RMVar_ID_70327 Human_SNP_ID_668419223 m1A Human chr19 - 49665680 49665680 49665680 CAGCCTCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCC CAGCCTCGAGTTTGAGAGCTACCCGGAGCTCCGAGACAGGGGTGGGTTCCAGCTGCCCGCACGCC T C IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49665525..49665733 32194978 MeRIP-seq:(Medium) rs1216699824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27277197 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 70328 RMVar_ID_70328 Human_SNP_ID_668419449 m1A Human chr19 - 49666052 49666052 49666052 GTCAACACCCCGCTGACCTGGTCCGGGGCCCCACCGCCGCCTCCTCCACTCAACTTGCGGTCTCC GTCAACACCCCGCTGACCTGGTCCGGGGCCCCGCCGCCGCCTCCTCCACTCAACTTGCGGTCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49665976..49666856;chr19:49665976..49666110 26863196 MeRIP-seq:(Medium) rs1283216050 Functional Loss SNV dbSNP153 33..33 33 - - - 70329 RMVar_ID_70329 Human_SNP_ID_668419784 m1A Human chr19 + 49667134 49667134 49667134 CCTCTGAGTCCCCTCGGCCTTGCTCTCTGCCCATCCGCCCCTGCTATGGTTTAGAGCCTGGTAAG CCTCTGAGTCCCCTCGGCCTTGCTCTCTGCCCGTCCGCCCCTGCTATGGTTTAGAGCCTGGTAAG A G BCL2L12 Ensembl:ENSG00000126453 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49667087..49668875 26863196 MeRIP-seq:(Medium) rs749948441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9382804,Human_RBP_ID_13496598,Human_RBP_ID_17657302 Human_Splice_Rec_2031567,Human_Splice_Rec_2031579,Human_Splice_Rec_2031589,Human_Splice_Rec_2031599,Human_Splice_Rec_2031611,Human_Splice_Rec_2031643,Human_Splice_Rec_2031651 RMVar_hsa_circ_91535,RMVar_hsa_circ_81815,RMVar_hsa_circ_195897,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899 70330 RMVar_ID_70330 Human_SNP_ID_668419785 m1A Human chr19 + 49667134 49667134 49667134 CCTCTGAGTCCCCTCGGCCTTGCTCTCTGCCCATCCGCCCCTGCTATGGTTTAGAGCCTGGTAAG CCTCTGAGTCCCCTCGGCCTTGCTCTCTGCCCTTCCGCCCCTGCTATGGTTTAGAGCCTGGTAAG A T BCL2L12 Ensembl:ENSG00000126453 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49667087..49668875 26863196 MeRIP-seq:(Medium) rs749948441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9382804,Human_RBP_ID_13496598,Human_RBP_ID_17657302 Human_Splice_Rec_2031567,Human_Splice_Rec_2031579,Human_Splice_Rec_2031589,Human_Splice_Rec_2031599,Human_Splice_Rec_2031611,Human_Splice_Rec_2031643,Human_Splice_Rec_2031651 RMVar_hsa_circ_91535,RMVar_hsa_circ_81815,RMVar_hsa_circ_195897,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899 70331 RMVar_ID_70331 Human_SNP_ID_668420633 m1A Human chr19 - 49670182 49670182 49670182 TGTAGGGTGGAAGAGGCAGGGTCCGCGTCAGCAGCGCCCCCGGGGCCAGCCAATAGAGGGCCGGG TGTAGGGTGGAAGAGGCAGGGTCCGCGTCAGCGGCGCCCCCGGGGCCAGCCAATAGAGGGCCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49670178..49670327 26863196 MeRIP-seq:(Medium) rs776469428 Functional Loss SNV dbSNP153 33..33 33 - - - 70332 RMVar_ID_70332 Human_SNP_ID_668420687 m1A Human chr19 - 49670267 49670267 49670267 GCTACAGAACAGCTCCACCAGGCGGGCGAAAGAGTCGGAGGACAGGCGGACCAGCTTGCTGCGCA GCTACAGAACAGCTCCACCAGGCGGGCGAAAGGGTCGGAGGACAGGCGGACCAGCTTGCTGCGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49670201..49670450 26863196 MeRIP-seq:(Medium) rs1370438790 Functional Loss SNV dbSNP153 33..33 33 - - - 70333 RMVar_ID_70333 Human_SNP_ID_668422710 m1A Human chr19 + 49677261 49677261 49677261 GAGGAGAAAGGGGGGGTCTTGGCGGCCGGAGGAGGAGTAGGTGCGGGTGAAGATGGCGGCAGCCG GAGGAGAAAGGGGGGGTCTTGGCGGCCGGAGGGGGAGTAGGTGCGGGTGAAGATGGCGGCAGCCG A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs200221062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241500,Human_RBP_ID_773189,Human_RBP_ID_3955407,Human_RBP_ID_4542850,Human_RBP_ID_5145382,Human_RBP_ID_5320528,Human_RBP_ID_5499986,Human_RBP_ID_9330207,Human_RBP_ID_9381312,Human_RBP_ID_17656331,Human_RBP_ID_17929500,Human_RBP_ID_18420971,Human_RBP_ID_18995297,Human_RBP_ID_22447964,Human_RBP_ID_22592362,Human_RBP_ID_22665812,Human_RBP_ID_23131690,Human_RBP_ID_26336629,Human_RBP_ID_26770084,Human_RBP_ID_26993732,Human_RBP_ID_27815594 Human_Splice_Rec_2031727,Human_Splice_Rec_2031745,Human_Splice_Rec_2031759,Human_Splice_Rec_2031769,Human_Splice_Rec_2031781,Human_Splice_Rec_2031783,Human_Splice_Rec_2031803,Human_Splice_Rec_2031813 70334 RMVar_ID_70334 Human_SNP_ID_668422721 m1A Human chr19 - 49677276 49677276 49677276 TGCAGTTCGCGGCCTCGGCTGCCGCCATCTTCACCCGCACCTACTCCTCCTCCGGCCGCCAAGAC TGCAGTTCGCGGCCTCGGCTGCCGCCATCTTCGCCCGCACCTACTCCTCCTCCGGCCGCCAAGAC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:49677226..49677350 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 70335 RMVar_ID_70335 Human_SNP_ID_668422722 m1A Human chr19 - 49677276 49677276 49677276 TGCAGTTCGCGGCCTCGGCTGCCGCCATCTTCACCCGCACCTACTCCTCCTCCGGCCGCCAAGAC TGCAGTTCGCGGCCTCGGCTGCCGCCATCTTCCCCCGCACCTACTCCTCCTCCGGCCGCCAAGAC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:49677226..49677350 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 70336 RMVar_ID_70336 Human_SNP_ID_668423484 m1A Human chr19 + 49679839 49679839 49679839 CGCCACCCAGCCCTCCCACAGCCACTCCCAGTAGCTAATCCTTTTTCCCTGTTACTCTCTCCTAG CGCCACCCAGCCCTCCCACAGCCACTCCCAGTGGCTAATCCTTTTTCCCTGTTACTCTCTCCTAG A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49679837..49679990 26863196 MeRIP-seq:(Medium) rs202071509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22663053 Human_Splice_Rec_2031785,Human_Splice_Rec_2031815,Human_Splice_Rec_2031845 70337 RMVar_ID_70337 Human_SNP_ID_668423487 m1A Human chr19 - 49679848 49679848 49679848 TACAAAATTCTAGGAGAGAGTAACAGGGAAAAAGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC TACAAAATTCTAGGAGAGAGTAACAGGGAAAATGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49679845..49679995;chr19:49679845..49679953 26863196 MeRIP-seq:(Medium) rs201580389 Functional Loss SNV dbSNP153 33..33 33 - - - 70338 RMVar_ID_70338 Human_SNP_ID_668423488 m1A Human chr19 - 49679848 49679848 49679848 TACAAAATTCTAGGAGAGAGTAACAGGGAAAAAGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC TACAAAATTCTAGGAGAGAGTAACAGGGAAAACGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49679845..49679995;chr19:49679845..49679953 26863196 MeRIP-seq:(Medium) rs201580389 Functional Loss SNV dbSNP153 33..33 33 - - - 70339 RMVar_ID_70339 Human_SNP_ID_668424243 m1A Human chr19 + 49682240 49682240 49682240 AGTATCTCTGATTATGCGGTGAAGATCGTCAAAGCCAACAAGTTAGACCACGGTGAGCCCAGAAA AGTATCTCTGATTATGCGGTGAAGATCGTCAAGGCCAACAAGTTAGACCACGGTGAGCCCAGAAA A G PRMT1 Ensembl:ENSG00000126457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr19:49681865..49682304;chr19:49682062..49683668 26863196,32194978 MeRIP-seq:(Medium) rs1188472192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525502,Human_RBP_ID_1569790,Human_RBP_ID_1890998,Human_RBP_ID_3575201,Human_RBP_ID_3957367,Human_RBP_ID_8492235,Human_RBP_ID_13496847,Human_RBP_ID_18737649,Human_RBP_ID_18998510,Human_RBP_ID_22448957,Human_RBP_ID_23211356 Human_Splice_Rec_2031672,Human_Splice_Rec_2031673,Human_Splice_Rec_2031684,Human_Splice_Rec_2031685,Human_Splice_Rec_2031702,Human_Splice_Rec_2031703,Human_Splice_Rec_2031720,Human_Splice_Rec_2031721,Human_Splice_Rec_2031732,Human_Splice_Rec_2031733,Human_Splice_Rec_2031750,Human_Splice_Rec_2031751,Human_Splice_Rec_2031766,Human_Splice_Rec_2031767,Human_Splice_Rec_2031774,Human_Splice_Rec_2031775,Human_Splice_Rec_2031790,Human_Splice_Rec_2031791,Human_Splice_Rec_2031808,Human_Splice_Rec_2031809,Human_Splice_Rec_2031820,Human_Splice_Rec_2031821,Human_Splice_Rec_2031834,Human_Splice_Rec_2031840,Human_Splice_Rec_2031841,Human_Splice_Rec_2031850 RMVar_hsa_circ_104811,RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,RMVar_hsa_circ_195904,RMVar_hsa_circ_127875,RMVar_hsa_circ_102156,RMVar_hsa_circ_195911,RMVar_hsa_circ_195906,RMVar_hsa_circ_195908,RMVar_hsa_circ_195909,RMVar_hsa_circ_195907,RMVar_hsa_circ_297570,RMVar_hsa_circ_317798,RMVar_hsa_circ_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_304264,RMVar_hsa_circ_195912,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 70340 RMVar_ID_70340 Human_SNP_ID_668425280 m1A Human chr19 - 49685103 49685103 49685103 GGCCAACATTCTGGGCCCCAAAGTCCCATGCCAGGGCCAGGTGATGGCCTCTCTTTGGTTTCAAC GGCCAACATTCTGGGCCCCAAAGTCCCATGCCTGGGCCAGGTGATGGCCTCTCTTTGGTTTCAAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49685100..49685501 32194978 MeRIP-seq:(Medium) rs1283773332 Functional Loss SNV dbSNP153 33..33 33 - - - 70341 RMVar_ID_70341 Human_SNP_ID_668425818 m1A Human chr19 + 49686703 49686703 49686703 AGACGGGCGAGGAGATCTTCGGCACCATCGGCATGCGGCCCAACGCCAAGAACAACGTGAGGCTC AGACGGGCGAGGAGATCTTCGGCACCATCGGCCTGCGGCCCAACGCCAAGAACAACGTGAGGCTC A C PRMT1 Ensembl:ENSG00000126457 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49686601..49686750 26863196 MeRIP-seq:(Medium) rs776399308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525509,Human_RBP_ID_9381317 Human_Splice_Rec_2031694,Human_Splice_Rec_2031695,Human_Splice_Rec_2031742,Human_Splice_Rec_2031743,Human_Splice_Rec_2031756,Human_Splice_Rec_2031757,Human_Splice_Rec_2031800,Human_Splice_Rec_2031801,Human_Splice_Rec_2031860,Human_Splice_Rec_2031861,Human_Splice_Rec_2031864 RMVar_hsa_circ_79411,RMVar_hsa_circ_127875,RMVar_hsa_circ_102156,RMVar_hsa_circ_195911,RMVar_hsa_circ_195908,RMVar_hsa_circ_195909,RMVar_hsa_circ_297570,RMVar_hsa_circ_107574,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195916,RMVar_hsa_circ_106360,RMVar_hsa_circ_195919,RMVar_hsa_circ_195920,RMVar_hsa_circ_334652,RMVar_hsa_circ_195922,RMVar_hsa_circ_308899 70342 RMVar_ID_70342 Human_SNP_ID_668425829 m1A Human chr19 - 49686728 49686728 49686728 TGCCACCCTCCCACCCAGCTGCCCGGAGCCTCACGTTGTTCTTGGCGTTGGGCCGCATGCCGATG TGCCACCCTCCCACCCAGCTGCCCGGAGCCTCCCGTTGTTCTTGGCGTTGGGCCGCATGCCGATG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49686576..49686756 26863196 MeRIP-seq:(Medium) rs879114659 Functional Loss SNV dbSNP153 33..33 33 - - - 70343 RMVar_ID_70343 Human_SNP_ID_668426149 m1A Human chr19 + 49687650 49687650 49687650 AAATGTCCTGCAGCCACAGGACCACCCCCTACAAAGACTCATGCAGCCCCCGGGACCACGGCACT AAATGTCCTGCAGCCACAGGACCACCCCCTACGAAGACTCATGCAGCCCCCGGGACCACGGCACT A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49687648..49687849 26863196 MeRIP-seq:(Medium) rs1485720874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569820,Human_RBP_ID_13496927,Human_RBP_ID_20412534,Human_RBP_ID_22811827 RMVar_hsa_circ_79411,RMVar_hsa_circ_127875,RMVar_hsa_circ_195911,RMVar_hsa_circ_195909,RMVar_hsa_circ_107574,RMVar_hsa_circ_195916,RMVar_hsa_circ_106360,RMVar_hsa_circ_195919 70344 RMVar_ID_70344 Human_SNP_ID_668426349 m1A Human chr19 - 49688121 49688121 49688121 AGAGGTGGGGCATGAGGGCGGAACCCACCAGGAGGTGGTGGCGGGGGGCGGGTGCAGGCAGGCTA AGAGGTGGGGCATGAGGGCGGAACCCACCAGGGGGTGGTGGCGGGGGGCGGGTGCAGGCAGGCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49688119..49688350 26863196 MeRIP-seq:(Medium) rs765000411 Functional Loss SNV dbSNP153 33..33 33 - - - 70345 RMVar_ID_70345 Human_SNP_ID_668434318 m1A Human chr19 + 49712821 49712819 49712821 GCATCTGTTTGACGTCCACAATTACCCGGACTATGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA GCATCTGTTTGACGTCCACAATTACCCGGAC__TGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA CTA C CPT1C Ensembl:ENSG00000169169 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49712733..49712834 26863410 MeRIP-seq:(Medium) rs1341198369 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1017580 Human_Splice_Rec_2031908,Human_Splice_Rec_2031909,Human_Splice_Rec_2031948,Human_Splice_Rec_2031949,Human_Splice_Rec_2032010,Human_Splice_Rec_2032011,Human_Splice_Rec_2032062,Human_Splice_Rec_2032063,Human_Splice_Rec_2032106,Human_Splice_Rec_2032107,Human_Splice_Rec_2032222,Human_Splice_Rec_2032223,Human_Splice_Rec_2032227,Human_Splice_Rec_2032231 RMVar_hsa_circ_195924,RMVar_hsa_circ_123917,RMVar_hsa_circ_367328,RMVar_hsa_circ_195925,RMVar_hsa_circ_78674,RMVar_hsa_circ_195929,RMVar_hsa_circ_195935 70346 RMVar_ID_70346 Human_SNP_ID_668434319 m1A Human chr19 + 49712821 49712821 49712821 GCATCTGTTTGACGTCCACAATTACCCGGACTATGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA GCATCTGTTTGACGTCCACAATTACCCGGACTGTGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA A G CPT1C Ensembl:ENSG00000169169 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49712733..49712834 26863410 MeRIP-seq:(Medium) rs1161252718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017580 Human_Splice_Rec_2031908,Human_Splice_Rec_2031909,Human_Splice_Rec_2031948,Human_Splice_Rec_2031949,Human_Splice_Rec_2032010,Human_Splice_Rec_2032011,Human_Splice_Rec_2032062,Human_Splice_Rec_2032063,Human_Splice_Rec_2032106,Human_Splice_Rec_2032107,Human_Splice_Rec_2032222,Human_Splice_Rec_2032223,Human_Splice_Rec_2032227,Human_Splice_Rec_2032231 RMVar_hsa_circ_195924,RMVar_hsa_circ_123917,RMVar_hsa_circ_367328,RMVar_hsa_circ_195925,RMVar_hsa_circ_78674,RMVar_hsa_circ_195929,RMVar_hsa_circ_195935 70347 RMVar_ID_70347 Human_SNP_ID_668436450 m1A Human chr19 - 49720053 49720053 49720053 CAACATGCCAGTGGCCCGGAGCTGGGTTTGTCACAAAACTTATGTGACCCCGCGGAGACCCTTCG CAACATGCCAGTGGCCCGGAGCTGGGTTTGTCGCAAAACTTATGTGACCCCGCGGAGACCCTTCG T C AC011495.1 Ensembl:ENSG00000243829 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879196815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21892354 Human_miRNA_ID_1908237 70348 RMVar_ID_70348 Human_SNP_ID_668449449 m1A Human chr19 + 49767115 49767115 49767115 CGCTGCTCTGTGCCCTGTCCGGCCAGGCCTGGAGCCGACACCACCGCCATCATGCCGGCCGTGTC CGCTGCTCTGTGCCCTGTCCGGCCAGGCCTGGGGCCGACACCACCGCCATCATGCCGGCCGTGTC A G AP2A1 Ensembl:ENSG00000196961 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49767001..49767242 26863196 MeRIP-seq:(Medium) rs532037606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241959,Human_RBP_ID_4557667,Human_RBP_ID_22533471,Human_RBP_ID_26816225 Human_Splice_Rec_2032273,Human_Splice_Rec_2032315,Human_Splice_Rec_2032327,Human_Splice_Rec_2032371 70349 RMVar_ID_70349 Human_SNP_ID_668454952 m1A Human chr19 + 49788494 49788494 49788494 GCAGAGTTTGGCCCAGAGTCAGGACTCGGGAGATGCGCTGTGGCTCAGGAGATGTGTGCCGTGGC GCAGAGTTTGGCCCAGAGTCAGGACTCGGGAGGTGCGCTGTGGCTCAGGAGATGTGTGCCGTGGC A G AP2A1 Ensembl:ENSG00000196961 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49788490..49788742 26863196 MeRIP-seq:(Medium) rs1185692322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13497181 RMVar_hsa_circ_63805,RMVar_hsa_circ_343360 70350 RMVar_ID_70350 Human_SNP_ID_668455829 m1A Human chr19 - 49792023 49792023 49792023 GTCATTGAGCAGGTGTACCACACGCGCCGTCCACTCGCCCATGGGCACCAGGTCAGGCGAGGCCT GTCATTGAGCAGGTGTACCACACGCGCCGTCCCCTCGCCCATGGGCACCAGGTCAGGCGAGGCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49791885..49792125 26863196 MeRIP-seq:(Medium) rs1344568687 Functional Loss SNV dbSNP153 33..33 33 - - - 70351 RMVar_ID_70351 Human_SNP_ID_668456967 m1A Human chr19 + 49795683 49795683 49795683 GACCTCCAGGACTACACCTACTACTTCGTCCCAGCACCCTGGCTCTCGGTGAAGCTCCTGCGGCT GACCTCCAGGACTACACCTACTACTTCGTCCCTGCACCCTGGCTCTCGGTGAAGCTCCTGCGGCT A T AP2A1 Ensembl:ENSG00000196961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49795582..49795782 26863196 MeRIP-seq:(Medium) rs1416253271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914923,Human_RBP_ID_3957384,Human_RBP_ID_17929542,Human_RBP_ID_22975442 Human_Splice_Rec_2032284,Human_Splice_Rec_2032285,Human_Splice_Rec_2032326,Human_Splice_Rec_2032338,Human_Splice_Rec_2032339,Human_Splice_Rec_2032378,Human_Splice_Rec_2032379 RMVar_hsa_circ_63805,RMVar_hsa_circ_343360,RMVar_hsa_circ_111802,RMVar_hsa_circ_40014,RMVar_hsa_circ_374684,RMVar_hsa_circ_195940,RMVar_hsa_circ_195941 70352 RMVar_ID_70352 Human_SNP_ID_668458116 m1A Human chr19 + 49799941 49799941 49799941 GGTGAGTGAAAGCCCGACATGGCCTGCGGCACACTCTCTCTCACACGCCCCGGCGGCAGGTCCTG GGTGAGTGAAAGCCCGACATGGCCTGCGGCACGCTCTCTCTCACACGCCCCGGCGGCAGGTCCTG A G AP2A1 Ensembl:ENSG00000196961 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49799938..49800017 26863196 MeRIP-seq:(Medium) rs73590490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090717 Human_Splice_Rec_2032387 RMVar_hsa_circ_63805,RMVar_hsa_circ_111802,RMVar_hsa_circ_34253,RMVar_hsa_circ_195941 70353 RMVar_ID_70353 Human_SNP_ID_668458117 m1A Human chr19 + 49799941 49799941 49799941 GGTGAGTGAAAGCCCGACATGGCCTGCGGCACACTCTCTCTCACACGCCCCGGCGGCAGGTCCTG GGTGAGTGAAAGCCCGACATGGCCTGCGGCACTCTCTCTCTCACACGCCCCGGCGGCAGGTCCTG A T AP2A1 Ensembl:ENSG00000196961 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49799938..49800017 26863196 MeRIP-seq:(Medium) rs73590490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090717 Human_Splice_Rec_2032387 RMVar_hsa_circ_63805,RMVar_hsa_circ_111802,RMVar_hsa_circ_34253,RMVar_hsa_circ_195941 70354 RMVar_ID_70354 Human_SNP_ID_668458594 m1A Human chr19 + 49801508 49801508 49801508 AGTTCATCAACCTCTTCCCCGAGACCAAGGCCACCATCCAGGGCGTCCTGCGGGCCGGCTCCCAG AGTTCATCAACCTCTTCCCCGAGACCAAGGCCGCCATCCAGGGCGTCCTGCGGGCCGGCTCCCAG A G AP2A1 Ensembl:ENSG00000196961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49801376..49801636 26863196 MeRIP-seq:(Medium) rs1428586269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525555,Human_RBP_ID_826307,Human_RBP_ID_4543005,Human_RBP_ID_8839464,Human_RBP_ID_17929547,Human_RBP_ID_18998521,Human_RBP_ID_22447968,Human_RBP_ID_22533204 Human_miRNA_ID_1957743,Human_miRNA_ID_1998970 RMVar_hsa_circ_63805,RMVar_hsa_circ_111802,RMVar_hsa_circ_195941,RMVar_hsa_circ_22226 70355 RMVar_ID_70355 Human_SNP_ID_668458846 m1A Human chr19 - 49802006 49802006 49802006 CTGCCGGGGGAGGGGCTGCCCGCAGCCCCAGGAGGTCGGCGGAGGGCGAGGGCGTCGACTGTAGG CTGCCGGGGGAGGGGCTGCCCGCAGCCCCAGGGGGTCGGCGGAGGGCGAGGGCGTCGACTGTAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49801976..49802025 26863196 MeRIP-seq:(Medium) rs868261837 Functional Loss SNV dbSNP153 33..33 33 - - - 70356 RMVar_ID_70356 Human_SNP_ID_668461234 m1A Human chr19 - 49808488 49808488 49808488 CGCTCTGCATCACCGCCTTTTCCTCCCAGCAGAGCCTTCACCAGAACAGCGCCGGCGCCTCCTCC CGCTCTGCATCACCGCCTTTTCCTCCCAGCAGGGCCTTCACCAGAACAGCGCCGGCGCCTCCTCC T C FUZ Ensembl:ENSG00000010361 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49808408..49809596 32194978 MeRIP-seq:(Medium) rs142342064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2032444,Human_Splice_Rec_2032445,Human_Splice_Rec_2032462,Human_Splice_Rec_2032463,Human_Splice_Rec_2032466,Human_Splice_Rec_2032467,Human_Splice_Rec_2032486,Human_Splice_Rec_2032487,Human_Splice_Rec_2032506,Human_Splice_Rec_2032507,Human_Splice_Rec_2032524,Human_Splice_Rec_2032525,Human_Splice_Rec_2032544,Human_Splice_Rec_2032545,Human_Splice_Rec_2032550 Human_miRNA_ID_881281 RMVar_hsa_circ_58493,RMVar_hsa_circ_104419,RMVar_hsa_circ_195944 70357 RMVar_ID_70357 Human_SNP_ID_668461623 m1A Human chr19 + 49809203 49809203 49809203 ACAACTGGCTGAGGGGTGGGCTCGGCCCGCAGAGTAGACACAGCTCCAGGCTCGGCAGCAGAGTC ACAACTGGCTGAGGGGTGGGCTCGGCCCGCAGCGTAGACACAGCTCCAGGCTCGGCAGCAGAGTC A C AC006942.1 Ensembl:ENSG00000269194 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49809153..49809224 26863196 MeRIP-seq:(Medium) rs527949286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589087,Human_RBP_ID_5587308 70358 RMVar_ID_70358 Human_SNP_ID_668461624 m1A Human chr19 + 49809203 49809203 49809203 ACAACTGGCTGAGGGGTGGGCTCGGCCCGCAGAGTAGACACAGCTCCAGGCTCGGCAGCAGAGTC ACAACTGGCTGAGGGGTGGGCTCGGCCCGCAGTGTAGACACAGCTCCAGGCTCGGCAGCAGAGTC A T AC006942.1 Ensembl:ENSG00000269194 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49809153..49809224 26863196 MeRIP-seq:(Medium) rs527949286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589087,Human_RBP_ID_5587308 70359 RMVar_ID_70359 Human_SNP_ID_668462329 m1A Human chr19 + 49811431 49811413 49811431 CACACACTGGGTCAGGTCCCCGATGAGCTCCGAGTCCCCCAGGAAGCTGTCGATGAGGCAATAAC CACACACTGGGTCAG__________________GTCCCCCAGGAAGCTGTCGATGAGGCAATAAC GGTCCCCGATGAGCTCCGA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49811380..49811481 32194978 MeRIP-seq:(Medium) rs1265839813 Functional Loss DEL dbSNP153 16..33 33 - - - 70360 RMVar_ID_70360 Human_SNP_ID_668462337 m1A Human chr19 + 49811431 49811431 49811431 CACACACTGGGTCAGGTCCCCGATGAGCTCCGAGTCCCCCAGGAAGCTGTCGATGAGGCAATAAC CACACACTGGGTCAGGTCCCCGATGAGCTCCGTGTCCCCCAGGAAGCTGTCGATGAGGCAATAAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49811380..49811481 32194978 MeRIP-seq:(Medium) rs767351327 Functional Loss SNV dbSNP153 33..33 33 - - - 70361 RMVar_ID_70361 Human_SNP_ID_668464534 m1A Human chr19 - 49818341 49818341 49818341 GCGCGGGCCGGGCCCTCGGACCCGGGGACCATACCCCGTGCGGTACCCGCCACCACCACTGCAGC GCGCGGGCCGGGCCCTCGGACCCGGGGACCATCCCCCGTGCGGTACCCGCCACCACCACTGCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49818276..49818573 26863196 MeRIP-seq:(Medium) rs756977834 Functional Loss SNV dbSNP153 33..33 33 - - - 70362 RMVar_ID_70362 Human_SNP_ID_668464537 m1A Human chr19 - 49818346 49818346 49818346 TCCCGGCGCGGGCCGGGCCCTCGGACCCGGGGACCATACCCCGTGCGGTACCCGCCACCACCACT TCCCGGCGCGGGCCGGGCCCTCGGACCCGGGGGCCATACCCCGTGCGGTACCCGCCACCACCACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49818301..49818421;chr19:49818301..49818425 26863196 MeRIP-seq:(Medium) rs1433763452 Functional Loss SNV dbSNP153 33..33 33 - - - 70363 RMVar_ID_70363 Human_SNP_ID_668464569 m1A Human chr19 + 49818409 49818409 49818409 GAGCGTGGTGGCCGACGTGGTGTTTGTGATTGAGGGTACGGCCAACCTGGGACCCTACTTCGAGG GAGCGTGGTGGCCGACGTGGTGTTTGTGATTGCGGGTACGGCCAACCTGGGACCCTACTTCGAGG A C MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49818322..49818410 26863410 MeRIP-seq:(Medium) rs1382112071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525602,Human_RBP_ID_1569887,Human_RBP_ID_4558679 Human_Splice_Rec_2032625,Human_Splice_Rec_2032645,Human_Splice_Rec_2032663,Human_Splice_Rec_2032671,Human_Splice_Rec_2032681,Human_Splice_Rec_2032683,Human_Splice_Rec_2032687,Human_Splice_Rec_2032721,Human_Splice_Rec_2032755,Human_Splice_Rec_2032767,Human_Splice_Rec_2032791,Human_Splice_Rec_2032803 70364 RMVar_ID_70364 Human_SNP_ID_668466944 m1A Human chr19 - 49826379 49826379 49826379 GGGCGCTGCTCCCAACCCACCACACACTTCCCAGCCCTCCTCTTCCTAGCCATCAAAACAGCTTT GGGCGCTGCTCCCAACCCACCACACACTTCCCCGCCCTCCTCTTCCTAGCCATCAAAACAGCTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49826369..49826487 26863196 MeRIP-seq:(Medium) rs938306873 Functional Loss SNV dbSNP153 33..33 33 - - - 70365 RMVar_ID_70365 Human_SNP_ID_668468403 m1A Human chr19 - 49830722 49830722 49830722 GCCTGGCTGAAGGGGGGACCCACTCCGGGAGCAGCTTGTTGGAGAGGGGTGATGGGCGAGACTGT GCCTGGCTGAAGGGGGGACCCACTCCGGGAGCCGCTTGTTGGAGAGGGGTGATGGGCGAGACTGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49830578..49830840 26863196 MeRIP-seq:(Medium) rs760327666 Functional Loss SNV dbSNP153 33..33 33 - - - 70366 RMVar_ID_70366 Human_SNP_ID_668468691 m1A Human chr19 + 49831438 49831438 49831438 AGCAGTCAGTCTCCAATAAGCTTCTGGCCTGGAGCGGGGTCCTGGAGTGGCAAGAGGTGAGGGGC AGCAGTCAGTCTCCAATAAGCTTCTGGCCTGGGGCGGGGTCCTGGAGTGGCAAGAGGTGAGGGGC A G MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49831387..49831482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_908868,Human_RBP_ID_3955440,Human_RBP_ID_18995312 Human_Splice_Rec_2032629,Human_Splice_Rec_2032705,Human_Splice_Rec_2032739,Human_Splice_Rec_2032775,Human_Splice_Rec_2032807,Human_Splice_Rec_2032825 70367 RMVar_ID_70367 Human_SNP_ID_668470074 m1A Human chr19 + 49835914 49835914 49835914 CCTTCGGCCCCAGAACCCTGGGGCCAACCCTCAGCTGCGAAGCCTCCTCCTCAACCCACCACCGG CCTTCGGCCCCAGAACCCTGGGGCCAACCCTCGGCTGCGAAGCCTCCTCCTCAACCCACCACCGG A G MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49835863..49836004 26863196 MeRIP-seq:(Medium) rs1425868838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241294,Human_RBP_ID_18947251,Human_RBP_ID_27816640 Human_Splice_Rec_2032641,Human_Splice_Rec_2032666,Human_Splice_Rec_2032667,Human_Splice_Rec_2032717,Human_Splice_Rec_2032751,Human_Splice_Rec_2032787,Human_Splice_Rec_2032819,Human_Splice_Rec_2032833 70368 RMVar_ID_70368 Human_SNP_ID_668470195 m1A Human chr19 - 49836260 49836260 49836260 GCGCAGGAGCCCCTGGTGGCTGGAGGTGGTGGAGGGAGGCCTGGGGTGGGGGCACCCCAGTCTGC GCGCAGGAGCCCCTGGTGGCTGGAGGTGGTGGGGGGAGGCCTGGGGTGGGGGCACCCCAGTCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr19:49835776..49836425;chr19:49835891..49836272 26863196,32194978 MeRIP-seq:(Medium) rs1287392262 Functional Loss SNV dbSNP153 33..33 33 - - - 70369 RMVar_ID_70369 Human_SNP_ID_668470241 m1A Human chr19 + 49836350 49836350 49836350 GGGGCAGCCCCAGTTGGGGCCCCCACTCCTGCATCCACCACCTGCCCAGTCCTGGCCCGCACAAC GGGGCAGCCCCAGTTGGGGCCCCCACTCCTGCCTCCACCACCTGCCCAGTCCTGGCCCGCACAAC A C MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49835016..49836471 32194978 MeRIP-seq:(Medium) rs564170396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525610 Human_Splice_Rec_2032643,Human_Splice_Rec_2032661,Human_Splice_Rec_2032669,Human_Splice_Rec_2032679,Human_Splice_Rec_2032719,Human_Splice_Rec_2032753,Human_Splice_Rec_2032789,Human_Splice_Rec_2032821 70370 RMVar_ID_70370 Human_SNP_ID_668470490 m1A Human chr19 + 49836906 49836906 49836906 GGGGCCCGGTCCCCCAGCCGGGCCTGCAGCCCAGCGTCATGGAGGACGACATCCTCATGGATCTC GGGGCCCGGTCCCCCAGCCGGGCCTGCAGCCCGGCGTCATGGAGGACGACATCCTCATGGATCTC A G MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:49836818..49836919 32194978 MeRIP-seq:(Medium) rs766379322 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_241296,Human_RBP_ID_8492332 Human_Splice_Rec_2032644,Human_Splice_Rec_2032662,Human_Splice_Rec_2032670,Human_Splice_Rec_2032680,Human_Splice_Rec_2032720,Human_Splice_Rec_2032766,Human_Splice_Rec_2032790,Human_Splice_Rec_2032822 70371 RMVar_ID_70371 Human_SNP_ID_668474376 m1A Human chr19 - 49851313 49851288 49851314 CGGCGCGGACGGACCATGGCGGGCGCGGGCCGAGCGGGCGGGGAGCTGCCGCGGGCCACAAGGGG CGGCGCGGACGGACCATGGCGGGCGCGGGCC__________________________ACAAGGGG TGGCCCGCGGCAGCTCCCCGCCCGCTC T PTOV1-AS1 Ensembl:ENSG00000268006 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49850770..49851627;chr19:49851151..49851500;chr19:49850572..49851676;chr19:49850671..49851627 26863196 MeRIP-seq:(Medium) rs1456911496 Functional Loss DEL dbSNP153 32..57 33 - - - Human_RBP_ID_3583957,Human_RBP_ID_8199776 70372 RMVar_ID_70372 Human_SNP_ID_668474382 m1A Human chr19 - 49851313 49851309 49851313 CGGCGCGGACGGACCATGGCGGGCGCGGGCCGAGCGGGCGGGGAGCTGCCGCGGGCCACAAGGGG CGGCGCGGACGGACCATGGCGGGCGCGGGCCG____GGCGGGGAGCTGCCGCGGGCCACAAGGGG CCGCT C PTOV1-AS1 Ensembl:ENSG00000268006 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49850770..49851627;chr19:49851151..49851500;chr19:49850572..49851676;chr19:49850671..49851627 26863196 MeRIP-seq:(Medium) rs993065501 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3583957,Human_RBP_ID_8199776 70373 RMVar_ID_70373 Human_SNP_ID_668475543 m1A Human chr19 - 49854357 49854357 49854357 GATAGGTGGGAAAACTGAGGCCGGGGCCTGCAAGGACAGGCAGTCCCCACACACCCCAGAGGGGA GATAGGTGGGAAAACTGAGGCCGGGGCCTGCAGGGACAGGCAGTCCCCACACACCCCAGAGGGGA T C AC018766.1 Ensembl:ENSG00000268047 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49854353..49854694 26863410 MeRIP-seq:(Medium) rs760000749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588972 70374 RMVar_ID_70374 Human_SNP_ID_668475715 m1A Human chr19 + 49854722 49854722 49854722 GCGGACCCTGCCCTGCCAAGCCTACGTGAACCAAGGCGAGAACCTGTGAGTGCCGGGGCGTGGCA GCGGACCCTGCCCTGCCAAGCCTACGTGAACCGAGGCGAGAACCTGTGAGTGCCGGGGCGTGGCA A G PTOV1 Ensembl:ENSG00000104960 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49854620..49854833 26863196 MeRIP-seq:(Medium) rs202190749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18192459,Human_RBP_ID_18998539,Human_RBP_ID_26816240 Human_Splice_Rec_2032848,Human_Splice_Rec_2032849,Human_Splice_Rec_2032860,Human_Splice_Rec_2032861,Human_Splice_Rec_2032884,Human_Splice_Rec_2032885,Human_Splice_Rec_2032908,Human_Splice_Rec_2032909,Human_Splice_Rec_2032932,Human_Splice_Rec_2032933,Human_Splice_Rec_2032940,Human_Splice_Rec_2032941,Human_Splice_Rec_2032948,Human_Splice_Rec_2032949,Human_Splice_Rec_2032966,Human_Splice_Rec_2032967,Human_Splice_Rec_2032990,Human_Splice_Rec_2032991,Human_Splice_Rec_2033012,Human_Splice_Rec_2033013,Human_Splice_Rec_2033036,Human_Splice_Rec_2033037,Human_Splice_Rec_2033060,Human_Splice_Rec_2033066,Human_Splice_Rec_2033067,Human_Splice_Rec_2033072,Human_Splice_Rec_2033073 RMVar_hsa_circ_19584,RMVar_hsa_circ_79440,RMVar_hsa_circ_97741,RMVar_hsa_circ_319424,RMVar_hsa_circ_195948,RMVar_hsa_circ_28570,RMVar_hsa_circ_195949 70375 RMVar_ID_70375 Human_SNP_ID_668475888 m1A Human chr19 - 49854986 49854984 49854986 AGTGGAACTGTGCCAACTGGGAGTTCCGGAACAGGGGGCCCAGGGTGGTCTGGGGGCGACAGGAC AGTGGAACTGTGCCAACTGGGAGTTCCGGAAC__GGGGCCCAGGGTGGTCTGGGGGCGACAGGAC CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49854401..49856278 32194978 MeRIP-seq:(Medium) rs1568641324 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_2033119 70376 RMVar_ID_70376 Human_SNP_ID_668475905 m1A Human chr19 + 49855016 49855016 49855016 CCTGTTCCGGAACTCCCAGTTGGCACAGTTCCACTTCACCAACAGAGACTGCGACTCGCTCAAGG CCTGTTCCGGAACTCCCAGTTGGCACAGTTCCGCTTCACCAACAGAGACTGCGACTCGCTCAAGG A G PTOV1 Ensembl:ENSG00000104960 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49854885..49855116 26863196 MeRIP-seq:(Medium) rs1568641455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569902,Human_RBP_ID_1891053,Human_RBP_ID_5421763,Human_RBP_ID_9382812,Human_RBP_ID_17270284,Human_RBP_ID_18737782 Human_Splice_Rec_2032852,Human_Splice_Rec_2032853,Human_Splice_Rec_2032864,Human_Splice_Rec_2032865,Human_Splice_Rec_2032888,Human_Splice_Rec_2032889,Human_Splice_Rec_2032912,Human_Splice_Rec_2032913,Human_Splice_Rec_2032936,Human_Splice_Rec_2032944,Human_Splice_Rec_2032952,Human_Splice_Rec_2032953,Human_Splice_Rec_2032970,Human_Splice_Rec_2032971,Human_Splice_Rec_2032994,Human_Splice_Rec_2032995,Human_Splice_Rec_2033016,Human_Splice_Rec_2033017,Human_Splice_Rec_2033040,Human_Splice_Rec_2033041,Human_Splice_Rec_2033070 RMVar_hsa_circ_79440,RMVar_hsa_circ_97741,RMVar_hsa_circ_319424,RMVar_hsa_circ_195948,RMVar_hsa_circ_28570,RMVar_hsa_circ_102989,RMVar_hsa_circ_195949,RMVar_hsa_circ_346831,RMVar_hsa_circ_195950 70377 RMVar_ID_70377 Human_SNP_ID_668475924 m1A Human chr19 - 49855043 49855043 49855043 AGCCGTTGCCCATGATGCGGCAGAGCCCCTTGAGCGAGTCGCAGTCTCTGTTGGTGAAGTGGAAC AGCCGTTGCCCATGATGCGGCAGAGCCCCTTGGGCGAGTCGCAGTCTCTGTTGGTGAAGTGGAAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49855026..49855050 26863196 MeRIP-seq:(Medium) rs371396128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13497657 Human_Splice_Rec_2033119 70378 RMVar_ID_70378 Human_SNP_ID_668476198 m1A Human chr19 - 49855763 49855763 49855763 AAATTCCCTCCCTCCAGCCTCCCGGTGGCCCTAGGAAGCACGGCTCCCCTGTCCTCCCTACCTCA AAATTCCCTCCCTCCAGCCTCCCGGTGGCCCTGGGAAGCACGGCTCCCCTGTCCTCCCTACCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49855300..49855936;chr19:49855251..49856475 26863196 MeRIP-seq:(Medium) rs1209838404 Functional Loss SNV dbSNP153 33..33 33 - - - 70379 RMVar_ID_70379 Human_SNP_ID_668476507 m1A Human chr19 + 49856581 49856581 49856581 CCCGGTTTTACAGATGATGGAGGCCCAGAAGCAGGAGGTGGCTGGTGTTAGGTCACACAGCTAGG CCCGGTTTTACAGATGATGGAGGCCCAGAAGCCGGAGGTGGCTGGTGTTAGGTCACACAGCTAGG A C PTOV1 Ensembl:ENSG00000104960 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49856579..49856669 26863196 MeRIP-seq:(Medium) rs1271483957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7816,Human_RBP_ID_239540,Human_RBP_ID_770601,Human_RBP_ID_824883,Human_RBP_ID_5193345,Human_RBP_ID_8103197,Human_RBP_ID_8728092,Human_RBP_ID_9929740 RMVar_hsa_circ_97741,RMVar_hsa_circ_319424,RMVar_hsa_circ_195948,RMVar_hsa_circ_28570,RMVar_hsa_circ_346831 70380 RMVar_ID_70380 Human_SNP_ID_668476647 m1A Human chr19 + 49856940 49856940 49856940 TCCAGGGTGGTGGGGGCACAGTGGCCCCGGGCAGTGACCACAGGGTCCTGACCCGCGGCCCCCGC TCCAGGGTGGTGGGGGCACAGTGGCCCCGGGCGGTGACCACAGGGTCCTGACCCGCGGCCCCCGC A G PTOV1 Ensembl:ENSG00000104960 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49856934..49857125 26863196 MeRIP-seq:(Medium) rs374118414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826103,Human_RBP_ID_3955451,Human_RBP_ID_5191750,Human_RBP_ID_8728094,Human_RBP_ID_18995320,Human_RBP_ID_22546264,Human_RBP_ID_22665850,Human_RBP_ID_22742048,Human_RBP_ID_25440843 RMVar_hsa_circ_97741,RMVar_hsa_circ_319424,RMVar_hsa_circ_195948,RMVar_hsa_circ_28570,RMVar_hsa_circ_346831 70381 RMVar_ID_70381 Human_SNP_ID_668476853 m1A Human chr19 - 49857309 49857309 49857309 AAGACCCACCCTCCAGCCCTGCAGAGCCGCCCAGTGGCCGCTTTTCCATGGAGCCCTGGTGGGAA AAGACCCACCCTCCAGCCCTGCAGAGCCGCCCGGTGGCCGCTTTTCCATGGAGCCCTGGTGGGAA T C PTOV1-AS2 Ensembl:ENSG00000269352 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49857258..49857473 26863196 MeRIP-seq:(Medium) rs1448934641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5099399 70382 RMVar_ID_70382 Human_SNP_ID_668477290 m1A Human chr19 + 49858140 49858140 49858140 GCTGCTGGTGAGGGGCTGGGGCCGGGTGCTGGAGCCTGCACGCAGTAGCTCTTCCAGAGGGCGGG GCTGCTGGTGAGGGGCTGGGGCCGGGTGCTGGGGCCTGCACGCAGTAGCTCTTCCAGAGGGCGGG A G PTOV1 Ensembl:ENSG00000104960 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49858126..49858286 26863196 MeRIP-seq:(Medium) rs780444391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090736,Human_RBP_ID_21979413,Human_RBP_ID_22592381,Human_RBP_ID_26785966 Human_Splice_Rec_2032872,Human_Splice_Rec_2032896,Human_Splice_Rec_2032920,Human_Splice_Rec_2032960,Human_Splice_Rec_2032978,Human_Splice_Rec_2033002,Human_Splice_Rec_2033024,Human_Splice_Rec_2033048,Human_Splice_Rec_2033084,Human_Splice_Rec_2033090,Human_Splice_Rec_2033104,Human_Splice_Rec_2033108 RMVar_hsa_circ_319424,RMVar_hsa_circ_294410,RMVar_hsa_circ_30203,RMVar_hsa_circ_341378,RMVar_hsa_circ_195952 70383 RMVar_ID_70383 Human_SNP_ID_668477525 m1A Human chr19 - 49858651 49858651 49858651 CCCTCCCCTGCGTCTGCTGGCACCACTCACGAAGCCATTGTCCATGATCCGGCACAGGCTCTTCA CCCTCCCCTGCGTCTGCTGGCACCACTCACGAGGCCATTGTCCATGATCCGGCACAGGCTCTTCA T C PTOV1-AS2 Ensembl:ENSG00000269352 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49858284..49858719 26863196 MeRIP-seq:(Medium) rs756588283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569924 Human_Splice_Rec_2033127 70384 RMVar_ID_70384 Human_SNP_ID_668478161 m1A Human chr19 + 49860037 49860037 49860037 CCTACAAAGCATCGTGTGAGATCCGCGTGCTTATGCTCCTGTACTCTTCAGAGAAGAAAATCTTC CCTACAAAGCATCGTGTGAGATCCGCGTGCTTCTGCTCCTGTACTCTTCAGAGAAGAAAATCTTC A C PTOV1 Ensembl:ENSG00000104960 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49859981..49861354 32194978 MeRIP-seq:(Medium) rs765850303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017614,Human_RBP_ID_5321854,Human_RBP_ID_8492372,Human_RBP_ID_8836453,Human_RBP_ID_17656334,Human_RBP_ID_18737812,Human_RBP_ID_23180012 Human_Splice_Rec_2032876,Human_Splice_Rec_2032924,Human_Splice_Rec_2032982,Human_Splice_Rec_2033006,Human_Splice_Rec_2033028,Human_Splice_Rec_2033052,Human_Splice_Rec_2033094 RMVar_hsa_circ_319424,RMVar_hsa_circ_28943,RMVar_hsa_circ_294410,RMVar_hsa_circ_341378,RMVar_hsa_circ_195952,RMVar_hsa_circ_195953,RMVar_hsa_circ_117063 70385 RMVar_ID_70385 Human_SNP_ID_668479431 m1A Human chr19 - 49861796 49861796 49861796 GCAAGGGAAACGGGTCGCCATCGACAACACAAACCCAGACGCCGCGAGCCGCGCCAGGTAGCGTG GCAAGGGAAACGGGTCGCCATCGACAACACAAGCCCAGACGCCGCGAGCCGCGCCAGGTAGCGTG T C PNKP Ensembl:ENSG00000039650 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49861503..49861856 26863196 MeRIP-seq:(Medium) rs541840060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957417,Human_RBP_ID_9381324,Human_RBP_ID_18998569 Human_Splice_Rec_2033146,Human_Splice_Rec_2033168,Human_Splice_Rec_2033169,Human_Splice_Rec_2033196,Human_Splice_Rec_2033197,Human_Splice_Rec_2033226,Human_Splice_Rec_2033227,Human_Splice_Rec_2033288,Human_Splice_Rec_2033289,Human_Splice_Rec_2033296,Human_Splice_Rec_2033322,Human_Splice_Rec_2033323,Human_Splice_Rec_2033352,Human_Splice_Rec_2033353,Human_Splice_Rec_2033382,Human_Splice_Rec_2033383,Human_Splice_Rec_2033389,Human_Splice_Rec_2033402,Human_Splice_Rec_2033403 Clinvar_Rec_286 RMVar_hsa_circ_102134,RMVar_hsa_circ_113881,RMVar_hsa_circ_122453,RMVar_hsa_circ_107249,RMVar_hsa_circ_195955,RMVar_hsa_circ_195957,RMVar_hsa_circ_195958,RMVar_hsa_circ_195956 70386 RMVar_ID_70386 Human_SNP_ID_668479432 m1A Human chr19 - 49861796 49861796 49861796 GCAAGGGAAACGGGTCGCCATCGACAACACAAACCCAGACGCCGCGAGCCGCGCCAGGTAGCGTG GCAAGGGAAACGGGTCGCCATCGACAACACAACCCCAGACGCCGCGAGCCGCGCCAGGTAGCGTG T G PNKP Ensembl:ENSG00000039650 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49861503..49861856 26863196 MeRIP-seq:(Medium) rs541840060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957417,Human_RBP_ID_9381324,Human_RBP_ID_18998569 Human_Splice_Rec_2033146,Human_Splice_Rec_2033168,Human_Splice_Rec_2033169,Human_Splice_Rec_2033196,Human_Splice_Rec_2033197,Human_Splice_Rec_2033226,Human_Splice_Rec_2033227,Human_Splice_Rec_2033288,Human_Splice_Rec_2033289,Human_Splice_Rec_2033296,Human_Splice_Rec_2033322,Human_Splice_Rec_2033323,Human_Splice_Rec_2033352,Human_Splice_Rec_2033353,Human_Splice_Rec_2033382,Human_Splice_Rec_2033383,Human_Splice_Rec_2033389,Human_Splice_Rec_2033402,Human_Splice_Rec_2033403 Clinvar_Rec_286 RMVar_hsa_circ_102134,RMVar_hsa_circ_113881,RMVar_hsa_circ_122453,RMVar_hsa_circ_107249,RMVar_hsa_circ_195955,RMVar_hsa_circ_195957,RMVar_hsa_circ_195958,RMVar_hsa_circ_195956 70387 RMVar_ID_70387 Human_SNP_ID_668479591 m1A Human chr19 + 49862009 49862009 49862009 CAAACCAGTTGAGAGGTGGAGATGGGAACTTTATAATAGATTTGGGGCGGCAAAAGCCTGGTCAT CAAACCAGTTGAGAGGTGGAGATGGGAACTTTGTAATAGATTTGGGGCGGCAAAAGCCTGGTCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49862001..49862104 26863196 MeRIP-seq:(Medium) rs759892733 Functional Loss SNV dbSNP153 33..33 33 - - - 70388 RMVar_ID_70388 Human_SNP_ID_668479592 m1A Human chr19 + 49862009 49862009 49862009 CAAACCAGTTGAGAGGTGGAGATGGGAACTTTATAATAGATTTGGGGCGGCAAAAGCCTGGTCAT CAAACCAGTTGAGAGGTGGAGATGGGAACTTTTTAATAGATTTGGGGCGGCAAAAGCCTGGTCAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49862001..49862104 26863196 MeRIP-seq:(Medium) rs759892733 Functional Loss SNV dbSNP153 33..33 33 - - - 70389 RMVar_ID_70389 Human_SNP_ID_668480181 m1A Human chr19 + 49862771 49862771 49862771 CTACGGGAGACGGTAGTGAGGAGGCCCTTCCCACAAATGTCCCCCCGCAGCGGTAGCGGGTCCCT CTACGGGAGACGGTAGTGAGGAGGCCCTTCCCTCAAATGTCCCCCCGCAGCGGTAGCGGGTCCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49862764..49863045 26863196 MeRIP-seq:(Medium) rs1013976753 Functional Loss SNV dbSNP153 33..33 33 - - - 70390 RMVar_ID_70390 Human_SNP_ID_668481662 m1A Human chr19 + 49866302 49866302 49866302 GATTACAGGCTTGAGCCACCACGCCCGGCCCCAATCAGATTTTCCTAATGTACCCCTTCACTGAC GATTACAGGCTTGAGCCACCACGCCCGGCCCCGATCAGATTTTCCTAATGTACCCCTTCACTGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49866298..49866387 26863196 MeRIP-seq:(Medium) rs917989228 Functional Loss SNV dbSNP153 33..33 33 - - - 70391 RMVar_ID_70391 Human_SNP_ID_668481872 m1A Human chr19 + 49866875 49866875 49866875 CCTCCCTAAATCGGCTCGATCCCCTCTCCCCCAAAGGATCTAGCTAATTCTAAATCAAGCACAAA CCTCCCTAAATCGGCTCGATCCCCTCTCCCCCCAAGGATCTAGCTAATTCTAAATCAAGCACAAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49866853..49866945 26863196 MeRIP-seq:(Medium) rs1002955115 Functional Loss SNV dbSNP153 33..33 33 - - - 70392 RMVar_ID_70392 Human_SNP_ID_668481981 m1A Human chr19 + 49867157 49867157 49867157 TCCGAGGGCAGGAAGATGGGGGGCGCTCCCCCAGGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC TCCGAGGGCAGGAAGATGGGGGGCGCTCCCCCGGGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49867112..49867250 26863196 MeRIP-seq:(Medium) rs765919999 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70393 RMVar_ID_70393 Human_SNP_ID_668482017 m1A Human chr19 - 49867207 49867207 49867207 AGCCCGTTTACCTGCTCCCCAGGCCGGCACCCAGGATGGGCGAGGTGGAGGCCCCGGGCCGCTTG AGCCCGTTTACCTGCTCCCCAGGCCGGCACCCGGGATGGGCGAGGTGGAGGCCCCGGGCCGCTTG T C PNKP Ensembl:ENSG00000039650 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49867108..49867251 26863196 MeRIP-seq:(Medium) rs796052848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2033234,Human_Splice_Rec_2033264,Human_Splice_Rec_2033360,Human_Splice_Rec_2033452,Human_Splice_Rec_2033466,Human_Splice_Rec_2033486,Human_Splice_Rec_2033496,Human_Splice_Rec_2033502,Human_Splice_Rec_2033506,Human_Splice_Rec_2033510 70394 RMVar_ID_70394 Human_SNP_ID_668482139 m1A Human chr19 - 49867516 49867516 49867516 GCCGGCCGGGTTGCAGGCGGGGCACCTCGGGCAGGACCTCCCTGGTCGGAAGTGGCCGTGAGCCC GCCGGCCGGGTTGCAGGCGGGGCACCTCGGGCGGGACCTCCCTGGTCGGAAGTGGCCGTGAGCCC T C PNKP Ensembl:ENSG00000039650 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49867429..49867532 26863196 MeRIP-seq:(Medium) rs977169044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420974 Human_Splice_Rec_2033233,Human_Splice_Rec_2033263,Human_Splice_Rec_2033359,Human_Splice_Rec_2033485,Human_Splice_Rec_2033495,Human_Splice_Rec_2033501,Human_Splice_Rec_2033508,Human_Splice_Rec_2033509 70395 RMVar_ID_70395 Human_SNP_ID_668482143 m1A Human chr19 + 49867522 49867522 49867522 ACGGCCACTTCCGACCAGGGAGGTCCTGCCCGAGGTGCCCCGCCTGCAACCCGGCCGGCGGCGGT ACGGCCACTTCCGACCAGGGAGGTCCTGCCCGTGGTGCCCCGCCTGCAACCCGGCCGGCGGCGGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49867426..49867575 26863196 MeRIP-seq:(Medium) rs1442193510 Functional Loss SNV dbSNP153 33..33 33 - - - 70396 RMVar_ID_70396 Human_SNP_ID_668482691 m1A Human chr19 + 49869296 49869293 49869296 GGATGGATGGAACCAATGAAAGGGGGTGCCAGAGGCAGGGACAGTTTGGGGCCATCCCTGAGGGG GGATGGATGGAACCAATGAAAGGGGGTGCC___GGCAGGGACAGTTTGGGGCCATCCCTGAGGGG CAGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49869248..49869430 26863196 MeRIP-seq:(Medium) rs1390027948 Functional Loss DEL dbSNP153 31..33 33 - - - 70397 RMVar_ID_70397 Human_SNP_ID_668482701 m1A Human chr19 - 49869318 49869318 49869318 TCCCGACAACTTGTTCCCTGACCCCCTCAGGGATGGCCCCAAACTGTCCCTGCCTCTGGCACCCC TCCCGACAACTTGTTCCCTGACCCCCTCAGGGCTGGCCCCAAACTGTCCCTGCCTCTGGCACCCC T G PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49869267..49869363 26863196 MeRIP-seq:(Medium) rs1324325043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525676,Human_RBP_ID_1017619,Human_RBP_ID_5116396,Human_RBP_ID_17083342,Human_RBP_ID_17385170,Human_RBP_ID_17501211,Human_RBP_ID_17657311,Human_RBP_ID_17929606,Human_RBP_ID_18945884,Human_RBP_ID_24484750 Human_miRNA_ID_444780,Human_miRNA_ID_1267624,Human_miRNA_ID_1973898,Human_miRNA_ID_1976077,Human_miRNA_ID_2613868,Human_miRNA_ID_3002194 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 70398 RMVar_ID_70398 Human_SNP_ID_668482710 m1A Human chr19 + 49869332 49869332 49869332 AGGGACAGTTTGGGGCCATCCCTGAGGGGGTCAGGGAACAAGTTGTCGGGACGTGGGCAAAGACG AGGGACAGTTTGGGGCCATCCCTGAGGGGGTCGGGGAACAAGTTGTCGGGACGTGGGCAAAGACG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49869281..49869382 32194978 MeRIP-seq:(Medium) rs1370127812 Functional Loss SNV dbSNP153 33..33 33 - - - 70399 RMVar_ID_70399 Human_SNP_ID_668482798 m1A Human chr19 - 49869553 49869553 49869553 GCACGGCATTGGCTCCATCCCCTAGTCGCTGGACAGCTCTTTTTTTGATTGGCTCAAATCCTGTA GCACGGCATTGGCTCCATCCCCTAGTCGCTGGGCAGCTCTTTTTTTGATTGGCTCAAATCCTGTA T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49869504..49869655 26863196 MeRIP-seq:(Medium) rs909631133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525684,Human_RBP_ID_6779376,Human_RBP_ID_13497842,Human_RBP_ID_17270294,Human_RBP_ID_17385175,Human_RBP_ID_17501213,Human_RBP_ID_18737844,Human_RBP_ID_26469775,Human_RBP_ID_27470555 Human_miRNA_ID_1989156 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 70400 RMVar_ID_70400 Human_SNP_ID_668482910 m1A Human chr19 + 49869787 49869787 49869787 CTGGAAGGACGGCGGGGATTGGCAGAGGCGGGACAATCTTGGGAATGGGAGACGCAAGGAGGCCG CTGGAAGGACGGCGGGGATTGGCAGAGGCGGGGCAATCTTGGGAATGGGAGACGCAAGGAGGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49869736..49869960 26863196 MeRIP-seq:(Medium) rs1005886303 Functional Loss SNV dbSNP153 33..33 33 - - - 70401 RMVar_ID_70401 Human_SNP_ID_668482915 m1A Human chr19 + 49869799 49869799 49869799 CGGGGATTGGCAGAGGCGGGACAATCTTGGGAATGGGAGACGCAAGGAGGCCGGTCCCGGATCGG CGGGGATTGGCAGAGGCGGGACAATCTTGGGACTGGGAGACGCAAGGAGGCCGGTCCCGGATCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49869749..49869955 26863196 MeRIP-seq:(Medium) rs367860845 Functional Loss SNV dbSNP153 33..33 33 - - - 70402 RMVar_ID_70402 Human_SNP_ID_668482916 m1A Human chr19 + 49869799 49869799 49869799 CGGGGATTGGCAGAGGCGGGACAATCTTGGGAATGGGAGACGCAAGGAGGCCGGTCCCGGATCGG CGGGGATTGGCAGAGGCGGGACAATCTTGGGAGTGGGAGACGCAAGGAGGCCGGTCCCGGATCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49869749..49869955 26863196 MeRIP-seq:(Medium) rs367860845 Functional Loss SNV dbSNP153 33..33 33 - - - 70403 RMVar_ID_70403 Human_SNP_ID_668483055 m1A Human chr19 - 49869993 49869993 49869993 CATGCGCGCGCTGGTGCTGCGAGAGGCCGAGGACACCCAGGTCTTCGGGGACCTGCCACGGCCGC CATGCGCGCGCTGGTGCTGCGAGAGGCCGAGGTCACCCAGGTCTTCGGGGACCTGCCACGGCCGC T A PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49869976..49870000 26863196 MeRIP-seq:(Medium) rs1274133967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13497859,Human_RBP_ID_17929615 Human_Splice_Rec_2033518,Human_Splice_Rec_2033524,Human_Splice_Rec_2033532,Human_Splice_Rec_2033540,Human_Splice_Rec_2033548,Human_Splice_Rec_2033556 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 70404 RMVar_ID_70404 Human_SNP_ID_668483509 m1A Human chr19 + 49871553 49871553 49871553 CCTACCTCCCCACATTTGCCCCTCACCGGCCCATTCTCCTCATCTGATGACCGCGCCTCTGTCCT CCTACCTCCCCACATTTGCCCCTCACCGGCCCGTTCTCCTCATCTGATGACCGCGCCTCTGTCCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49871551..49871875 26863196 MeRIP-seq:(Medium) rs774716755 Functional Loss SNV dbSNP153 33..33 33 - - - 70405 RMVar_ID_70405 Human_SNP_ID_668483562 m1A Human chr19 + 49871672 49871672 49871672 CTGTGTGGGTAGGGCTGAGGCTGGGGGCACTGAGCAGGTGGGGGGGCCGGCGGGGGTCTCCTCGC CTGTGTGGGTAGGGCTGAGGCTGGGGGCACTGGGCAGGTGGGGGGGCCGGCGGGGGTCTCCTCGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:49871480..49871900 26863196 MeRIP-seq:(Medium) rs1234697325 Functional Loss SNV dbSNP153 33..33 33 - - - 70406 RMVar_ID_70406 Human_SNP_ID_668483563 m1A Human chr19 + 49871675 49871675 49871675 TGTGGGTAGGGCTGAGGCTGGGGGCACTGAGCAGGTGGGGGGGCCGGCGGGGGTCTCCTCGCTCA TGTGGGTAGGGCTGAGGCTGGGGGCACTGAGCGGGTGGGGGGGCCGGCGGGGGTCTCCTCGCTCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49871513..49871900 26863196 MeRIP-seq:(Medium) rs1470542095 Functional Loss SNV dbSNP153 33..33 33 - - - 70407 RMVar_ID_70407 Human_SNP_ID_668483671 m1A Human chr19 - 49871871 49871871 49871871 CAGGTCATCCACAGGGCTCTTTGTGATGGATGAGGACGCCACCCTCCAGGACCTTCCCCCCTTCT CAGGTCATCCACAGGGCTCTTTGTGATGGATGGGGACGCCACCCTCCAGGACCTTCCCCCCTTCT T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49871499..49873586;chr19:49871493..49873536 26863196 MeRIP-seq:(Medium) rs1224294478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131431,Human_RBP_ID_6779384,Human_RBP_ID_18998590 Human_Splice_Rec_2033514,Human_Splice_Rec_2033515,Human_Splice_Rec_2033520,Human_Splice_Rec_2033521,Human_Splice_Rec_2033528,Human_Splice_Rec_2033529,Human_Splice_Rec_2033536,Human_Splice_Rec_2033537,Human_Splice_Rec_2033544,Human_Splice_Rec_2033545,Human_Splice_Rec_2033552,Human_Splice_Rec_2033553 RMVar_hsa_circ_48764,RMVar_hsa_circ_127542,RMVar_hsa_circ_195962,RMVar_hsa_circ_377457,RMVar_hsa_circ_195964,RMVar_hsa_circ_95962 70408 RMVar_ID_70408 Human_SNP_ID_668484092 m1A Human chr19 - 49873159 49873159 49873159 GCCGCCACCACCCCGCCCGGGCCCCTGTGCCTATGCTGCCCATGGTCGAGGAGCCCTGGCGGAGG GCCGCCACCACCCCGCCCGGGCCCCTGTGCCTGTGCTGCCCATGGTCGAGGAGCCCTGGCGGAGG T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49873058..49873300 26863410 MeRIP-seq:(Medium) rs766406368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557672 Human_miRNA_ID_1938512,Human_miRNA_ID_1949612 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962,RMVar_hsa_circ_377457 70409 RMVar_ID_70409 Human_SNP_ID_668485147 m1A Human chr19 - 49876488 49876470 49876488 CTCACGGGAGGGGTATGGCCTGCACAGATCAGAGGGCAGAGGTCTGCCAGCGATCCTTTGCTGAG CTCACGGGAGGGGTATGGCCTGCACAGATCAG__________________CGATCCTTTGCTGAG GCTGGCAGACCTCTGCCCT G PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49876486..49876605 26863196 MeRIP-seq:(Medium) rs1168190825 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_3583962,Human_RBP_ID_8233884,Human_RBP_ID_9428347,Human_RBP_ID_22072067,Human_RBP_ID_22416920,Human_RBP_ID_23231903,Human_RBP_ID_26769868,Human_RBP_ID_26994013 70410 RMVar_ID_70410 Human_SNP_ID_668485151 m1A Human chr19 - 49876490 49876489 49876491 GGCTCACGGGAGGGGTATGGCCTGCACAGATCAGAGGGCAGAGGTCTGCCAGCGATCCTTTGCTG GGCTCACGGGAGGGGTATGGCCTGCACAGAT__GAGGGCAGAGGTCTGCCAGCGATCCTTTGCTG CTG C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49876484..49876600 26863196 MeRIP-seq:(Medium) rs1373278563 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3583962,Human_RBP_ID_8233884,Human_RBP_ID_9428347,Human_RBP_ID_22072067,Human_RBP_ID_22416920,Human_RBP_ID_23231903,Human_RBP_ID_26769868,Human_RBP_ID_26994013 70411 RMVar_ID_70411 Human_SNP_ID_668485244 m1A Human chr19 - 49876684 49876684 49876684 GGAGGCGGAGTGTGCGGAGAGGAGGCGGGGCAACTGCGCGGACGTGACGCAAGGCGCCGCCATGT GGAGGCGGAGTGTGCGGAGAGGAGGCGGGGCAGCTGCGCGGACGTGACGCAAGGCGCCGCCATGT T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49876671..49876822 26863196 MeRIP-seq:(Medium) rs1303752991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5370642 Human_Splice_Rec_2033549 70412 RMVar_ID_70412 Human_SNP_ID_668485473 m1A Human chr19 + 49877287 49877286 49877287 TTCGGCTCTTCCAGCTGTCGCGCCCCGCAGAGAGATGGGACAGCCCCGTATTAACATGGCCTTAG TTCGGCTCTTCCAGCTGTCGCGCCCCGCAGAG_GATGGGACAGCCCCGTATTAACATGGCCTTAG GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49877078..49877350 26863196 MeRIP-seq:(Medium) rs1476274360 Functional Loss DEL dbSNP153 33..33 33 - - - 70413 RMVar_ID_70413 Human_SNP_ID_668485474 m1A Human chr19 - 49877290 49877290 49877290 CAGCTAAGGCCATGTTAATACGGGGCTGTCCCATCTCTCTGCGGGGCGCGACAGCTGGAAGAGCC CAGCTAAGGCCATGTTAATACGGGGCTGTCCCTTCTCTCTGCGGGGCGCGACAGCTGGAAGAGCC T A PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49877040..49877332 26863196 MeRIP-seq:(Medium) rs1295512151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558685,Human_RBP_ID_5421766,Human_RBP_ID_18420975 Human_Splice_Rec_2033533 70414 RMVar_ID_70414 Human_SNP_ID_668485631 m1A Human chr19 + 49877721 49877714 49877721 GAGGAGGCGGGGCAGTGGGGCCTTCGGCGGCGACTATGGAAGGAGCCGGCTACAGGGTAAGCACT GAGGAGGCGGGGCAGTGGGGCCTTCG_______CTATGGAAGGAGCCGGCTACAGGGTAAGCACT GGCGGCGA G TBC1D17 Ensembl:ENSG00000104946 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49877675..49877786 26863196 MeRIP-seq:(Medium) rs776042059 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_18420977 Human_Splice_Rec_2033563,Human_Splice_Rec_2033593,Human_Splice_Rec_2033623,Human_Splice_Rec_2033641 70415 RMVar_ID_70415 Human_SNP_ID_668485655 m1A Human chr19 - 49877746 49877746 49877746 CACTGAAGCGAGGGAATGCGTCCTCAGTGCTTACCCTGTAGCCGGCTCCTTCCATAGTCGCCGCC CACTGAAGCGAGGGAATGCGTCCTCAGTGCTTTCCCTGTAGCCGGCTCCTTCCATAGTCGCCGCC T A PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49877706..49877789 26863196 MeRIP-seq:(Medium) rs1458037221 Functional Loss SNV dbSNP153 33..33 33 - - - 70416 RMVar_ID_70416 Human_SNP_ID_668485869 m1A Human chr19 - 49878171 49878171 49878171 CTCGGTCCTGATACTTCTTAGCGCTGGTGTGCAGGTACACTCCGCCCTTCTCAAACACCACCTGA CTCGGTCCTGATACTTCTTAGCGCTGGTGTGCGGGTACACTCCGCCCTTCTCAAACACCACCTGA T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49878132..49878359 26863196 MeRIP-seq:(Medium) rs1455365329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2033433,Human_Splice_Rec_2033511,Human_Splice_Rec_2033557,Human_Splice_Rec_2033561 70417 RMVar_ID_70417 Human_SNP_ID_668487303 m1A Human chr19 - 49882089 49882089 49882089 AGCTGCAGGTGGTGGAAGGAGTTGGAGAGAGCAGAGGAGTCGTGGGGGAAGACAAGGTAGAGGCG AGCTGCAGGTGGTGGAAGGAGTTGGAGAGAGCGGAGGAGTCGTGGGGGAAGACAAGGTAGAGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49882017..49882226 26863196 MeRIP-seq:(Medium) rs755474947 Functional Loss SNV dbSNP153 33..33 33 - - - 70418 RMVar_ID_70418 Human_SNP_ID_668489850 m1A Human chr19 - 49888415 49888415 49888415 CTCCTGCACGTTGTGGGGCAGCTCCTGGAGGCACGGGATGAGAGAAGCGAAAAGCGGAAGGTGAA CTCCTGCACGTTGTGGGGCAGCTCCTGGAGGCGCGGGATGAGAGAAGCGAAAAGCGGAAGGTGAA T C lnc-NUP62-1,lnc-NUP62-1:2,lnc-NUP62-1:3 RNACentral:URS00008B219F,RNACentral:URS00008C205B,RNACentral:URS00008BDD2D lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49888413..49888491 26863196 MeRIP-seq:(Medium) rs758056808 Functional Loss SNV dbSNP153 33..33 33 - - - 70419 RMVar_ID_70419 Human_SNP_ID_668489970 m1A Human chr19 + 49888608 49888608 49888608 CAGCCTGGAGATCCTGCCCGAGGAGGAGGACGAGGGCGCCGACTCCTAACCCCGCCAGGCAGCCT CAGCCTGGAGATCCTGCCCGAGGAGGAGGACGGGGGCGCCGACTCCTAACCCCGCCAGGCAGCCT A G TBC1D17 Ensembl:ENSG00000104946 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49888563..49888689 26863196 MeRIP-seq:(Medium) rs1198399608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241268 70420 RMVar_ID_70420 Human_SNP_ID_668495263 m1A Human chr19 - 49907075 49907075 49907075 CGGTCCCTGTCACATTTGTTAAATGAAAGAACAATGAAGCCCAGTGTAACGTCAGTCCACAGAAA CGGTCCCTGTCACATTTGTTAAATGAAAGAACGATGAAGCCCAGTGTAACGTCAGTCCACAGAAA T C IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49906973..49907074 32194978 MeRIP-seq:(Medium) rs902567575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569959,Human_RBP_ID_1891080,Human_RBP_ID_3575278,Human_RBP_ID_8197926,Human_RBP_ID_13498171,Human_RBP_ID_18306604,Human_RBP_ID_23804964,Human_RBP_ID_26472821 Human_miRNA_ID_1133146 70421 RMVar_ID_70421 Human_SNP_ID_668495552 m1A Human chr19 - 49907825 49907825 49907825 CCAAATGTAAGAGAACCTCCAAGTCAGGGCGCAGTGGCTCACCCCTGTAATCTCAGCACTTTGGG CCAAATGTAAGAGAACCTCCAAGTCAGGGCGCGGTGGCTCACCCCTGTAATCTCAGCACTTTGGG T C IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49907801..49907825 26863196 MeRIP-seq:(Medium) rs986097884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525720,Human_RBP_ID_1569969,Human_RBP_ID_1891088,Human_RBP_ID_3575284,Human_RBP_ID_6779431,Human_RBP_ID_13498197,Human_RBP_ID_17929645,Human_RBP_ID_23804971,Human_RBP_ID_26474275 70422 RMVar_ID_70422 Human_SNP_ID_668495582 m1A Human chr19 + 49907965 49907959 49907966 TCAGCACTTCTCCATCACCAGGCTGAGCCAGGATGAGGTGGGTGGTCGCAGTAGGTGAAAAGGGG TCAGCACTTCTCCATCACCAGGCTGAG_______GAGGTGGGTGGTCGCAGTAGGTGAAAAGGGG GCCAGGAT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49907769..49907969 32194978 MeRIP-seq:(Medium) rs1319093132 Functional Loss DEL dbSNP153 28..34 33 - - - 70423 RMVar_ID_70423 Human_SNP_ID_668495685 m1A Human chr19 - 49908288 49908288 49908288 GAGGAAGGTGGAGGAGGTGACCAAGGTGTGCGAGGGCCGGCGCAAGGAGCAGGAGCGCAGCTTCC GAGGAAGGTGGAGGAGGTGACCAAGGTGTGCGTGGGCCGGCGCAAGGAGCAGGAGCGCAGCTTCC T A IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49908167..49908417 32194978 MeRIP-seq:(Medium) rs1062800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6779448,Human_RBP_ID_27277369 70424 RMVar_ID_70424 Human_SNP_ID_668495793 m1A Human chr19 - 49908550 49908550 49908550 CACTGGAGGAGTTGGTCAAGGAGCAGAGCGGGACCATCTACCTGCAGCACGCGGATGAGGAGCGT CACTGGAGGAGTTGGTCAAGGAGCAGAGCGGGCCCATCTACCTGCAGCACGCGGATGAGGAGCGT T G IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49908501..49908575 32194978 MeRIP-seq:(Medium) rs375741773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017645,Human_RBP_ID_3955473,Human_RBP_ID_5527112,Human_RBP_ID_6779455,Human_RBP_ID_22070465,Human_RBP_ID_22449614,Human_RBP_ID_26338169,Human_RBP_ID_27277373 70425 RMVar_ID_70425 Human_SNP_ID_668495971 m1A Human chr19 - 49908967 49908967 49908967 CAACATCCACCGCTGCCACCGCCACCGCCACCACCACCAGCAGCAGCAGCACCACCGGCTTTGCC CAACATCCACCGCTGCCACCGCCACCGCCACCGCCACCAGCAGCAGCAGCACCACCGGCTTTGCC T C IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49908918..49909320 26863196 MeRIP-seq:(Medium) rs140091070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387489,Human_RBP_ID_22068144,Human_RBP_ID_26475134 Human_miRNA_ID_272474 70426 RMVar_ID_70426 Human_SNP_ID_668496038 m1A Human chr19 + 49909058 49909058 49909058 GGTGCCTTTAAGCTGAAGCCCTGTGTCCCAGCAGTGGGGGCGCCCGCTGTGGTCACAGGGGTACA GGTGCCTTTAAGCTGAAGCCCTGTGTCCCAGCGGTGGGGGCGCCCGCTGTGGTCACAGGGGTACA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr19:49908851..49909101;chr19:49909020..49909244 26863196 MeRIP-seq:(Medium) rs1399191388 Functional Loss SNV dbSNP153 33..33 33 - - - 70427 RMVar_ID_70427 Human_SNP_ID_668496050 m1A Human chr19 + 49909082 49909082 49909082 GTCCCAGCAGTGGGGGCGCCCGCTGTGGTCACAGGGGTACAGAGGGAGAGTCCAGTGGTGGCAGA GTCCCAGCAGTGGGGGCGCCCGCTGTGGTCACCGGGGTACAGAGGGAGAGTCCAGTGGTGGCAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49909031..49909171 26863196 MeRIP-seq:(Medium) rs754745409 Functional Loss SNV dbSNP153 33..33 33 - - - 70428 RMVar_ID_70428 Human_SNP_ID_668496051 m1A Human chr19 + 49909082 49909082 49909082 GTCCCAGCAGTGGGGGCGCCCGCTGTGGTCACAGGGGTACAGAGGGAGAGTCCAGTGGTGGCAGA GTCCCAGCAGTGGGGGCGCCCGCTGTGGTCACGGGGGTACAGAGGGAGAGTCCAGTGGTGGCAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49909031..49909171 26863196 MeRIP-seq:(Medium) rs754745409 Functional Loss SNV dbSNP153 33..33 33 - - - 70429 RMVar_ID_70429 Human_SNP_ID_668496171 m1A Human chr19 - 49909327 49909327 49909327 CTCCAGCTACCACATCTGGAGGCTTCTCATTCACTGGTGGAAGCACGGCCCAACCCTCCGGTTTC CTCCAGCTACCACATCTGGAGGCTTCTCATTCGCTGGTGGAAGCACGGCCCAACCCTCCGGTTTC T C IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49909276..49909425 32194978 MeRIP-seq:(Medium) rs987794938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1017651,Human_RBP_ID_4543603,Human_RBP_ID_6779468,Human_RBP_ID_8836490,Human_RBP_ID_17270317,Human_RBP_ID_17501225,Human_RBP_ID_17929666,Human_RBP_ID_18737885,Human_RBP_ID_22238179,Human_RBP_ID_27470624 70430 RMVar_ID_70430 Human_SNP_ID_668496290 m1A Human chr19 + 49909622 49909622 49909622 CCTGTCGTCTGTGTGGCCGGAGTCTGGGTGGCAAGTGAGAACAGGCCGGTGGAAGGGGTACTTGT CCTGTCGTCTGTGTGGCCGGAGTCTGGGTGGCGAGTGAGAACAGGCCGGTGGAAGGGGTACTTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49909573..49909678 26863196 MeRIP-seq:(Medium) rs1403727811 Functional Loss SNV dbSNP153 33..33 33 - - - 70431 RMVar_ID_70431 Human_SNP_ID_668502094 m1A Human chr19 - 49929322 49929322 49929322 AGAAGGTGGGAGCGGAGAGCGCAGGCGTGGTGAGCGCGGAGACGGGCCGGGGGCACAAAGGGGTC AGAAGGTGGGAGCGGAGAGCGCAGGCGTGGTGGGCGCGGAGACGGGCCGGGGGCACAAAGGGGTC T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:49929201..49929450 26863196 MeRIP-seq:(Medium) rs1342685784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_204585,Human_RBP_ID_773116,Human_RBP_ID_9330216,Human_RBP_ID_19090772 70432 RMVar_ID_70432 Human_SNP_ID_668502097 m1A Human chr19 + 49929327 49929327 49929327 CTTTGTGCCCCCGGCCCGTCTCCGCGCTCACCACGCCTGCGCTCTCCGCTCCCACCTTCTTTCTT CTTTGTGCCCCCGGCCCGTCTCCGCGCTCACCGCGCCTGCGCTCTCCGCTCCCACCTTCTTTCTT A G ATF5 Ensembl:ENSG00000169136 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49929226..49929729 26863410 MeRIP-seq:(Medium) rs1335136322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4572272,Human_RBP_ID_9329152,Human_RBP_ID_17387020,Human_RBP_ID_22446975,Human_RBP_ID_22763486 Human_Splice_Rec_2033968,Human_Splice_Rec_2033969,Human_Splice_Rec_2033973,Human_Splice_Rec_2033977,Human_Splice_Rec_2033979 70433 RMVar_ID_70433 Human_SNP_ID_668502119 m1A Human chr19 - 49929380 49929380 49929380 GCGGTTACTCACTCCATGGCTGCAGCAAGGAGAGGCGGCGGCGGCCTCGGCTGAAGAAAGAAGGT GCGGTTACTCACTCCATGGCTGCAGCAAGGAGCGGCGGCGGCGGCCTCGGCTGAAGAAAGAAGGT T G IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding 5'UTR,5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49929200..49929729 26863196 MeRIP-seq:(Medium) rs1349798107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145393,Human_RBP_ID_5421775,Human_RBP_ID_5469080,Human_RBP_ID_9330216,Human_RBP_ID_18421452,Human_RBP_ID_19090772,Human_RBP_ID_22449616,Human_RBP_ID_27815603 Human_Splice_Rec_2033771,Human_Splice_Rec_2033791,Human_Splice_Rec_2033809,Human_Splice_Rec_2033843,Human_Splice_Rec_2033851,Human_Splice_Rec_2033861,Human_Splice_Rec_2033865,Human_Splice_Rec_2033867,Human_Splice_Rec_2033871,Human_Splice_Rec_2033877,Human_Splice_Rec_2033883,Human_Splice_Rec_2033897,Human_Splice_Rec_2033903,Human_Splice_Rec_2033909,Human_Splice_Rec_2033915,Human_Splice_Rec_2033919,Human_Splice_Rec_2033923,Human_Splice_Rec_2033929,Human_Splice_Rec_2033935,Human_Splice_Rec_2033943,Human_Splice_Rec_2033947,Human_Splice_Rec_2033953,Human_Splice_Rec_2033959 70434 RMVar_ID_70434 Human_SNP_ID_668503401 m1A Human chr19 - 49932705 49932703 49932705 TAGATGGCCAGCAAGTCCAGAGTATCCAAGACAGGGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA TAGATGGCCAGCAAGTCCAGAGTATCCAAGAC__GGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA CCT C AC011452.2 Ensembl:ENSG00000269179 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49932654..49932803 32194978 MeRIP-seq:(Medium) rs1438909383 Functional Loss DEL dbSNP153 33..34 33 - - - 70435 RMVar_ID_70435 Human_SNP_ID_668503402 m1A Human chr19 - 49932705 49932704 49932705 TAGATGGCCAGCAAGTCCAGAGTATCCAAGACAGGGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA TAGATGGCCAGCAAGTCCAGAGTATCCAAGAC_GGGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA CT C AC011452.2 Ensembl:ENSG00000269179 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49932654..49932803 32194978 MeRIP-seq:(Medium) rs755645547 Functional Loss DEL dbSNP153 33..33 33 - - - 70436 RMVar_ID_70436 Human_SNP_ID_668503404 m1A Human chr19 - 49932705 49932705 49932705 TAGATGGCCAGCAAGTCCAGAGTATCCAAGACAGGGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA TAGATGGCCAGCAAGTCCAGAGTATCCAAGACGGGGGGCTGGGGGAGGTCAAAGGAGGGGAGGGA T C AC011452.2 Ensembl:ENSG00000269179 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49932654..49932803 32194978 MeRIP-seq:(Medium) rs1156715002 Functional Loss SNV dbSNP153 33..33 33 - - - 70437 RMVar_ID_70437 Human_SNP_ID_668503494 m1A Human chr19 + 49932875 49932875 49932875 CCCACATCCTGCCACCACCCGAGGGGACCGCAAGCAAAAGAAGAGAGACCAGAACAAGTCGGCGG CCCACATCCTGCCACCACCCGAGGGGACCGCATGCAAAAGAAGAGAGACCAGAACAAGTCGGCGG A T ATF5 Ensembl:ENSG00000169136 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:49932776..49932955 26863196 MeRIP-seq:(Medium) rs199986421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568742,Human_RBP_ID_26474281 70438 RMVar_ID_70438 Human_SNP_ID_668517659 m1A Human chr19 + 49979134 49979134 49979134 CCATCGGGAGGCCAATGGGGTCATATGGAGACACACGCAGATCCTGCAGCAAAGCTTCTAGGTTG CCATCGGGAGGCCAATGGGGTCATATGGAGACGCACGCAGATCCTGCAGCAAAGCTTCTAGGTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49979074..49979177 26863196 MeRIP-seq:(Medium) rs753013089 Functional Loss SNV dbSNP153 33..33 33 - - - 70439 RMVar_ID_70439 Human_SNP_ID_668518854 m1A Human chr19 - 49982995 49982994 49982995 AGGGCTGAGCTGGCCCCAGATCCATGGGGCAGAGGAGGACATGGGGCAGAGAGAGTTGAGAAACT AGGGCTGAGCTGGCCCCAGATCCATGGGGCAG_GGAGGACATGGGGCAGAGAGAGTTGAGAAACT CT C VRK3 Ensembl:ENSG00000105053 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49982987..49983070 26863196 MeRIP-seq:(Medium) rs1295907699 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_121137,RMVar_hsa_circ_116398,RMVar_hsa_circ_195973,RMVar_hsa_circ_195974,RMVar_hsa_circ_195976,RMVar_hsa_circ_288115,RMVar_hsa_circ_305939 70440 RMVar_ID_70440 Human_SNP_ID_668520042 m1A Human chr19 - 49987323 49987322 49987324 AGCACCAAGAACAGCAGGCAGCGGGACACAAAAGGGAAGTGCTAGGGATGTGGGTTCAGCACCAG AGCACCAAGAACAGCAGGCAGCGGGACACAA__GGGAAGTGCTAGGGATGTGGGTTCAGCACCAG CTT C VRK3 Ensembl:ENSG00000105053 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49987284..49987442;chr19:49987272..49987439 26863196 MeRIP-seq:(Medium) rs1355254820 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_121137,RMVar_hsa_circ_116398,RMVar_hsa_circ_195973,RMVar_hsa_circ_195974,RMVar_hsa_circ_195976,RMVar_hsa_circ_288115,RMVar_hsa_circ_305939 70441 RMVar_ID_70441 Human_SNP_ID_668520043 m1A Human chr19 - 49987323 49987323 49987323 AGCACCAAGAACAGCAGGCAGCGGGACACAAAAGGGAAGTGCTAGGGATGTGGGTTCAGCACCAG AGCACCAAGAACAGCAGGCAGCGGGACACAAAGGGGAAGTGCTAGGGATGTGGGTTCAGCACCAG T C VRK3 Ensembl:ENSG00000105053 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49987284..49987442;chr19:49987272..49987439 26863196 MeRIP-seq:(Medium) rs11882531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121137,RMVar_hsa_circ_116398,RMVar_hsa_circ_195973,RMVar_hsa_circ_195974,RMVar_hsa_circ_195976,RMVar_hsa_circ_288115,RMVar_hsa_circ_305939 70442 RMVar_ID_70442 Human_SNP_ID_668520047 m1A Human chr19 - 49987330 49987330 49987330 TGTGTTCAGCACCAAGAACAGCAGGCAGCGGGACACAAAAGGGAAGTGCTAGGGATGTGGGTTCA TGTGTTCAGCACCAAGAACAGCAGGCAGCGGGGCACAAAAGGGAAGTGCTAGGGATGTGGGTTCA T C VRK3 Ensembl:ENSG00000105053 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49987279..49987394 26863196 MeRIP-seq:(Medium) rs530496967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121137,RMVar_hsa_circ_116398,RMVar_hsa_circ_195973,RMVar_hsa_circ_195974,RMVar_hsa_circ_195976,RMVar_hsa_circ_288115,RMVar_hsa_circ_305939 70443 RMVar_ID_70443 Human_SNP_ID_668527967 m1A Human chr19 + 50014638 50014638 50014638 GAAGGCAGTGAAAGAGTGGGGCATGCAGGCCCATAAGGGAAGAGGCGTCCAGGAGGGAGCGGCAA GAAGGCAGTGAAAGAGTGGGGCATGCAGGCCCGTAAGGGAAGAGGCGTCCAGGAGGGAGCGGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50014630..50014718 26863196 MeRIP-seq:(Medium) rs1175950807 Functional Loss SNV dbSNP153 33..33 33 - - - 70444 RMVar_ID_70444 Human_SNP_ID_668536010 m1A Human chr19 - 50044202 50044202 50044202 CTTGGCACTATTTTCATTTGGTCTCTATCGAAATGTCTCAACTCCCTTCCTCTCCTCTCTTTATC CTTGGCACTATTTTCATTTGGTCTCTATCGAAGTGTCTCAACTCCCTTCCTCTCCTCTCTTTATC T C AC010624.3 Ensembl:ENSG00000269091 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50044151..50044371 26863196 MeRIP-seq:(Medium) rs1568410048 Functional Loss SNV dbSNP153 33..33 33 - - - 70445 RMVar_ID_70445 Human_SNP_ID_668552676 m1A Human chr19 - 50133817 50133817 50133817 CTCCGGCCGGTTGCGCGGGCCCTCGGACCCTCAGGGTAGGCGAGGGTTCGAGGGCACGAGTTCGA CTCCGGCCGGTTGCGCGGGCCCTCGGACCCTCCGGGTAGGCGAGGGTTCGAGGGCACGAGTTCGA T G SNAR-B1,SNAR-B1:2,RF02556-021,RF02556-021:2 RNACentral:URS0000574455,RNACentral:URS000002A4F1,RNACentral:URS0000317834,RNACentral:URS0000AB79F5 snRNA,snRNA,Other,Other intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1291482264 Functional Loss SNV dbSNP153 33..33 33 - - - 70446 RMVar_ID_70446 Human_SNP_ID_668574459 m1A Human chr19 + 50210595 50210595 50210595 GGCGGCGGCGCTGCGGGACGAAGGCGAGGAGGAGGCGGAGGTGGAGCTGGCGGAGAGCGGGAGGC GGCGGCGGCGCTGCGGGACGAAGGCGAGGAGGCGGCGGAGGTGGAGCTGGCGGAGAGCGGGAGGC A C MYH14 Ensembl:ENSG00000105357 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50210544..50210744 32194978 MeRIP-seq:(Medium) rs748365469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239694 Human_miRNA_ID_2017231 RMVar_hsa_circ_195982,RMVar_hsa_circ_126737 70447 RMVar_ID_70447 Human_SNP_ID_668595601 m1A Human chr19 - 50289585 50289585 50289585 CCAGCCTCATCACGGCCCTGCAGGTCACGCTCATGCTGAGTCTTGAGAGCCTGCACAGTCACCTC CCAGCCTCATCACGGCCCTGCAGGTCACGCTCCTGCTGAGTCTTGAGAGCCTGCACAGTCACCTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50286440..50308355 32194978 MeRIP-seq:(Medium) rs1340234478 Functional Loss SNV dbSNP153 33..33 33 - - - 70448 RMVar_ID_70448 Human_SNP_ID_668600739 m1A Human chr19 + 50309117 50309117 50309117 CGGCCGCCGGAGGCTGCAGCGTGAGCTGGAAGATGTCACAGAGTCGGCCGAGTCCATGAACCGTG CGGCCGCCGGAGGCTGCAGCGTGAGCTGGAAGTTGTCACAGAGTCGGCCGAGTCCATGAACCGTG A T MYH14 Ensembl:ENSG00000105357 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50309001..50309201 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2034631,Human_Splice_Rec_2034715,Human_Splice_Rec_2034769,Human_Splice_Rec_2034851,Human_Splice_Rec_2034931,Human_Splice_Rec_2035081,Human_Splice_Rec_2035119,Human_Splice_Rec_2035137 Human_miRNA_ID_2722747 RMVar_hsa_circ_122340,RMVar_hsa_circ_195985 70449 RMVar_ID_70449 Human_SNP_ID_668606213 m1A Human chr19 - 50328189 50328184 50328189 GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCCATCCACCCCACCCCCGCCTCTCCAGGCGCCCCC GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCC_____CCCCACCCCCGCCTCTCCAGGCGCCCCC GTGGAT G KCNC3 Ensembl:ENSG00000131398 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50328187..50328294 32194978 MeRIP-seq:(Medium) rs1199451227 Functional Loss DEL dbSNP153 33..37 33 - - - 70450 RMVar_ID_70450 Human_SNP_ID_668606217 m1A Human chr19 - 50328189 50328189 50328189 GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCCATCCACCCCACCCCCGCCTCTCCAGGCGCCCCC GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCCCTCCACCCCACCCCCGCCTCTCCAGGCGCCCCC T G KCNC3 Ensembl:ENSG00000131398 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50328187..50328294 32194978 MeRIP-seq:(Medium) rs1160198073 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70451 RMVar_ID_70451 Human_SNP_ID_668606218 m1A Human chr19 - 50328189 50328189 50328189 GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCCATCCACCCCACCCCCGCCTCTCCAGGCGCCCCC GCTGCCAGGGTGAGCGCGCTCTCGGGGCCCCCGTCCACCCCACCCCCGCCTCTCCAGGCGCCCCC T C KCNC3 Ensembl:ENSG00000131398 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50328187..50328294 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 70452 RMVar_ID_70452 Human_SNP_ID_668619198 m1A Human chr19 - 50376501 50376501 50376501 CCTGACACACCGCCGCTACTCAAATACCCTCAAAAGTAACTTCGCCACTTCTTCCGGCAACCCCG CCTGACACACCGCCGCTACTCAAATACCCTCATAAGTAACTTCGCCACTTCTTCCGGCAACCCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50376451..50376843 26863196 MeRIP-seq:(Medium) rs762406945 Functional Loss SNV dbSNP153 33..33 33 - - - 70453 RMVar_ID_70453 Human_SNP_ID_668619199 m1A Human chr19 - 50376501 50376501 50376501 CCTGACACACCGCCGCTACTCAAATACCCTCAAAAGTAACTTCGCCACTTCTTCCGGCAACCCCG CCTGACACACCGCCGCTACTCAAATACCCTCAGAAGTAACTTCGCCACTTCTTCCGGCAACCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50376451..50376843 26863196 MeRIP-seq:(Medium) rs762406945 Functional Loss SNV dbSNP153 33..33 33 - - - 70454 RMVar_ID_70454 Human_SNP_ID_668619312 m1A Human chr19 + 50376779 50376779 50376779 GGCCGTCCACGAGACCCCCGCGCGCAGCCATGAGCCCCGCCCCCCGCTGTTGCTTGGAGAGGGGC GGCCGTCCACGAGACCCCCGCGCGCAGCCATGCGCCCCGCCCCCCGCTGTTGCTTGGAGAGGGGC A C NR1H2 Ensembl:ENSG00000131408 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:50376736..50377253 32194978 MeRIP-seq:(Medium) rs902207975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911876,Human_RBP_ID_3957429,Human_RBP_ID_5238873,Human_RBP_ID_21978682,Human_RBP_ID_22476953,Human_RBP_ID_26472844 Human_Splice_Rec_2035170,Human_Splice_Rec_2035171,Human_Splice_Rec_2035184,Human_Splice_Rec_2035185,Human_Splice_Rec_2035208,Human_Splice_Rec_2035209,Human_Splice_Rec_2035226,Human_Splice_Rec_2035227,Human_Splice_Rec_2035232,Human_Splice_Rec_2035233,Human_Splice_Rec_2035250,Human_Splice_Rec_2035251,Human_Splice_Rec_2035268,Human_Splice_Rec_2035269,Human_Splice_Rec_2035283,Human_Splice_Rec_2035290,Human_Splice_Rec_2035291,Human_Splice_Rec_2035300,Human_Splice_Rec_2035301 70455 RMVar_ID_70455 Human_SNP_ID_668619313 m1A Human chr19 + 50376779 50376779 50376779 GGCCGTCCACGAGACCCCCGCGCGCAGCCATGAGCCCCGCCCCCCGCTGTTGCTTGGAGAGGGGC GGCCGTCCACGAGACCCCCGCGCGCAGCCATGGGCCCCGCCCCCCGCTGTTGCTTGGAGAGGGGC A G NR1H2 Ensembl:ENSG00000131408 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:50376736..50377253 32194978 MeRIP-seq:(Medium) rs902207975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911876,Human_RBP_ID_3957429,Human_RBP_ID_5238873,Human_RBP_ID_21978682,Human_RBP_ID_22476953,Human_RBP_ID_26472844 Human_Splice_Rec_2035170,Human_Splice_Rec_2035171,Human_Splice_Rec_2035184,Human_Splice_Rec_2035185,Human_Splice_Rec_2035208,Human_Splice_Rec_2035209,Human_Splice_Rec_2035226,Human_Splice_Rec_2035227,Human_Splice_Rec_2035232,Human_Splice_Rec_2035233,Human_Splice_Rec_2035250,Human_Splice_Rec_2035251,Human_Splice_Rec_2035268,Human_Splice_Rec_2035269,Human_Splice_Rec_2035283,Human_Splice_Rec_2035290,Human_Splice_Rec_2035291,Human_Splice_Rec_2035300,Human_Splice_Rec_2035301 70456 RMVar_ID_70456 Human_SNP_ID_668619335 m1A Human chr19 + 50376825 50376825 50376825 CTGTTGCTTGGAGAGGGGCGGGACCTGGAGAGAGGTGCGAGGGCGGAGCATGAATGGAGGAGGCG CTGTTGCTTGGAGAGGGGCGGGACCTGGAGAGCGGTGCGAGGGCGGAGCATGAATGGAGGAGGCG A C NR1H2 Ensembl:ENSG00000131408 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50376785..50377303 32194978 MeRIP-seq:(Medium) rs1475136416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5238873,Human_RBP_ID_22592408 Human_Splice_Rec_2035171,Human_Splice_Rec_2035185,Human_Splice_Rec_2035209,Human_Splice_Rec_2035227,Human_Splice_Rec_2035233,Human_Splice_Rec_2035251,Human_Splice_Rec_2035269,Human_Splice_Rec_2035283,Human_Splice_Rec_2035291,Human_Splice_Rec_2035301 70457 RMVar_ID_70457 Human_SNP_ID_668619336 m1A Human chr19 + 50376825 50376825 50376825 CTGTTGCTTGGAGAGGGGCGGGACCTGGAGAGAGGTGCGAGGGCGGAGCATGAATGGAGGAGGCG CTGTTGCTTGGAGAGGGGCGGGACCTGGAGAGGGGTGCGAGGGCGGAGCATGAATGGAGGAGGCG A G NR1H2 Ensembl:ENSG00000131408 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50376785..50377303 32194978 MeRIP-seq:(Medium) rs1475136416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5238873,Human_RBP_ID_22592408 Human_Splice_Rec_2035171,Human_Splice_Rec_2035185,Human_Splice_Rec_2035209,Human_Splice_Rec_2035227,Human_Splice_Rec_2035233,Human_Splice_Rec_2035251,Human_Splice_Rec_2035269,Human_Splice_Rec_2035283,Human_Splice_Rec_2035291,Human_Splice_Rec_2035301 70458 RMVar_ID_70458 Human_SNP_ID_668619723 m1A Human chr19 - 50377761 50377759 50377762 GGACCCTCCTCCTTTACAGTGGGTGAAGAAGAAGGGGCGCCAGGCTGAGGGGGGCCATTTCCTGG GGACCCTCCTCCTTTACAGTGGGTGAAGAAG___GGGCGCCAGGCTGAGGGGGGCCATTTCCTGG CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50377604..50377936 32194978 MeRIP-seq:(Medium) rs570889133 Functional Loss DEL dbSNP153 32..34 33 - - - 70459 RMVar_ID_70459 Human_SNP_ID_668619771 m1A Human chr19 + 50377838 50377838 50377838 CGGGGGTCCGGACCCTGATGTCCCAGGCACTGATGAGGCCAGCTCAGCCTGCAGCACAGACTGGG CGGGGGTCCGGACCCTGATGTCCCAGGCACTGGTGAGGCCAGCTCAGCCTGCAGCACAGACTGGG A G NR1H2 Ensembl:ENSG00000131408 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:50377787..50377887 32194978 MeRIP-seq:(Medium) rs1231648548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22449621,Human_RBP_ID_26472845 Human_Splice_Rec_2035189,Human_Splice_Rec_2035213,Human_Splice_Rec_2035237,Human_Splice_Rec_2035255,Human_Splice_Rec_2035273,Human_Splice_Rec_2035287,Human_Splice_Rec_2035295,Human_Splice_Rec_2035305,Human_Splice_Rec_2035321,Human_Splice_Rec_2035335 Human_miRNA_ID_2769380 RMVar_hsa_circ_120888,RMVar_hsa_circ_195991 70460 RMVar_ID_70460 Human_SNP_ID_668619987 m1A Human chr19 + 50378328 50378328 50378328 TCTTCCGGCGCAGTGTGGTCCGTGGTGGGGCCAGGCGCTATGCCTGCCGGGGTGGCGGAACCTGC TCTTCCGGCGCAGTGTGGTCCGTGGTGGGGCCCGGCGCTATGCCTGCCGGGGTGGCGGAACCTGC A C NR1H2 Ensembl:ENSG00000131408 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50378282..50378442 26863196 MeRIP-seq:(Medium) rs60638904 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8839475 RMVar_hsa_circ_120888,RMVar_hsa_circ_195991 70461 RMVar_ID_70461 Human_SNP_ID_668619988 m1A Human chr19 + 50378328 50378328 50378328 TCTTCCGGCGCAGTGTGGTCCGTGGTGGGGCCAGGCGCTATGCCTGCCGGGGTGGCGGAACCTGC TCTTCCGGCGCAGTGTGGTCCGTGGTGGGGCCTGGCGCTATGCCTGCCGGGGTGGCGGAACCTGC A T NR1H2 Ensembl:ENSG00000131408 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50378282..50378442 26863196 MeRIP-seq:(Medium) rs60638904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8839475 RMVar_hsa_circ_120888,RMVar_hsa_circ_195991 70462 RMVar_ID_70462 Human_SNP_ID_668620007 m1A Human chr19 + 50378376 50378376 50378376 GGGGTGGCGGAACCTGCCAGATGGACGCTTTCATGCGGCGCAAGTGCCAGCAGTGCCGGCTGCGC GGGGTGGCGGAACCTGCCAGATGGACGCTTTCGTGCGGCGCAAGTGCCAGCAGTGCCGGCTGCGC A G NR1H2 Ensembl:ENSG00000131408 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50378327..50378429 26863196 MeRIP-seq:(Medium) rs769480606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4543998,Human_RBP_ID_6779781,Human_RBP_ID_26336665 Human_Splice_Rec_2035215,Human_Splice_Rec_2035239,Human_Splice_Rec_2035257,Human_Splice_Rec_2035297,Human_Splice_Rec_2035307,Human_Splice_Rec_2035323,Human_Splice_Rec_2035337 RMVar_hsa_circ_120888,RMVar_hsa_circ_195991 70463 RMVar_ID_70463 Human_SNP_ID_668622757 m1A Human chr19 - 50385173 50385173 50385173 CCTCCTTCCATTCTTATTCCTGCTACAATCCAATTTCCACTCAGTGGTGAGTTTTTCAAAACATG CCTCCTTCCATTCTTATTCCTGCTACAATCCACTTTCCACTCAGTGGTGAGTTTTTCAAAACATG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50385171..50385452 26863196 MeRIP-seq:(Medium) rs552360693 Functional Loss SNV dbSNP153 33..33 33 - - - 70464 RMVar_ID_70464 Human_SNP_ID_668627044 m1A Human chr19 + 50398961 50398961 50398961 TGATGCACCTCGGCCATCCCAATTCGAGGAGGACCTGGCACTGATGGAGGAGATGGAGGCAGAAC TGATGCACCTCGGCCATCCCAATTCGAGGAGGTCCTGGCACTGATGGAGGAGATGGAGGCAGAAC A T POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:50398851..50398991 26863196 MeRIP-seq:(Medium) rs1486924942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1570071,Human_RBP_ID_1891155,Human_RBP_ID_5585865,Human_RBP_ID_6779819,Human_RBP_ID_8492564,Human_RBP_ID_8840186,Human_RBP_ID_9294536,Human_RBP_ID_17935080,Human_RBP_ID_18998621,Human_RBP_ID_22975541,Human_RBP_ID_23805224 Human_Splice_Rec_2035449,Human_Splice_Rec_2035499,Human_Splice_Rec_2035551,Human_Splice_Rec_2035605,Human_Splice_Rec_2035659,Human_Splice_Rec_2035705,Human_Splice_Rec_2035757,Human_Splice_Rec_2035809,Human_Splice_Rec_2035825 Human_miRNA_ID_2769381 RMVar_hsa_circ_76877,RMVar_hsa_circ_195993,RMVar_hsa_circ_195992,RMVar_hsa_circ_287397,RMVar_hsa_circ_195994,RMVar_hsa_circ_280249 70465 RMVar_ID_70465 Human_SNP_ID_668627156 m1A Human chr19 + 50399312 50399312 50399312 CCTCTGCCTGGCTCCTTTCAGAACCACATGCCATCCTGGCCGGGGAAGACCATGACTCCATGTAC CCTCTGCCTGGCTCCTTTCAGAACCACATGCCGTCCTGGCCGGGGAAGACCATGACTCCATGTAC A G POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50399308..50399425 26863196 MeRIP-seq:(Medium) rs957747242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76877,RMVar_hsa_circ_195993,RMVar_hsa_circ_195992,RMVar_hsa_circ_287397,RMVar_hsa_circ_195994,RMVar_hsa_circ_280249 70466 RMVar_ID_70466 Human_SNP_ID_668628285 m1A Human chr19 - 50401896 50401896 50401896 TCACCAGGGGGCGCTGGGGTGTAGAAGTAGGGAGCGAAGCCGTGGATGTGGCAGCAGACAGAGAA TCACCAGGGGGCGCTGGGGTGTAGAAGTAGGGGGCGAAGCCGTGGATGTGGCAGCAGACAGAGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50401751..50401944 26863196 MeRIP-seq:(Medium) rs935931842 Functional Loss SNV dbSNP153 33..33 33 - - - 70467 RMVar_ID_70467 Human_SNP_ID_668628415 m1A Human chr19 - 50402112 50402112 50402112 GATCCTGGGGGAGCACTCACTCTCTCGGGAGCACAGTTCCACAGCCAGCACGGCCGGCCCAGTCA GATCCTGGGGGAGCACTCACTCTCTCGGGAGCTCAGTTCCACAGCCAGCACGGCCGGCCCAGTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50401989..50402145 26863196 MeRIP-seq:(Medium) rs762498700 Functional Loss SNV dbSNP153 33..33 33 - - - 70468 RMVar_ID_70468 Human_SNP_ID_668628416 m1A Human chr19 - 50402112 50402112 50402112 GATCCTGGGGGAGCACTCACTCTCTCGGGAGCACAGTTCCACAGCCAGCACGGCCGGCCCAGTCA GATCCTGGGGGAGCACTCACTCTCTCGGGAGCCCAGTTCCACAGCCAGCACGGCCGGCCCAGTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50401989..50402145 26863196 MeRIP-seq:(Medium) rs762498700 Functional Loss SNV dbSNP153 33..33 33 - - - 70469 RMVar_ID_70469 Human_SNP_ID_668628426 m1A Human chr19 - 50402126 50402126 50402126 CCCTCCAACCCGCTGATCCTGGGGGAGCACTCACTCTCTCGGGAGCACAGTTCCACAGCCAGCAC CCCTCCAACCCGCTGATCCTGGGGGAGCACTCTCTCTCTCGGGAGCACAGTTCCACAGCCAGCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:50402115..50402198;chr19:50402116..50402199 26863196 MeRIP-seq:(Medium) rs1184160046 Functional Loss SNV dbSNP153 33..33 33 - - - 70470 RMVar_ID_70470 Human_SNP_ID_668628959 m1A Human chr19 - 50403152 50403152 50403152 CCTTGGCACCCAGGATGGGGGCACAGGGCCGCAGGGTGAGCGCCAGGCGTAGGAAGGGCTCCGGC CCTTGGCACCCAGGATGGGGGCACAGGGCCGCGGGGTGAGCGCCAGGCGTAGGAAGGGCTCCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50403104..50403246 26863196 MeRIP-seq:(Medium) rs143340270 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_287 70471 RMVar_ID_70471 Human_SNP_ID_668628960 m1A Human chr19 - 50403152 50403152 50403152 CCTTGGCACCCAGGATGGGGGCACAGGGCCGCAGGGTGAGCGCCAGGCGTAGGAAGGGCTCCGGC CCTTGGCACCCAGGATGGGGGCACAGGGCCGCCGGGTGAGCGCCAGGCGTAGGAAGGGCTCCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50403104..50403246 26863196 MeRIP-seq:(Medium) rs143340270 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_287 70472 RMVar_ID_70472 Human_SNP_ID_668630546 m1A Human chr19 - 50407331 50407331 50407331 ACTTCACCACGGGCATCAGCAGCCCCTCGTGCATGGCCTGGGAGGGGAGAAGGTGGGAAATGGAG ACTTCACCACGGGCATCAGCAGCCCCTCGTGCCTGGCCTGGGAGGGGAGAAGGTGGGAAATGGAG T G lnc-NAPSA-3 RNACentral:URS0000D5E39A lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50407326..50407400 32194978 MeRIP-seq:(Medium) rs748444470 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_288 70473 RMVar_ID_70473 Human_SNP_ID_668631189 m1A Human chr19 + 50409147 50409147 50409147 AACCCAGCCTGACTGAGGATCAGTTCATCAGGACCCCCACCGGGGACGAGTTTGTGAAGACCTCA AACCCAGCCTGACTGAGGATCAGTTCATCAGGGCCCCCACCGGGGACGAGTTTGTGAAGACCTCA A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50408877..50409197 32194978 MeRIP-seq:(Medium) rs201212113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52561,Human_RBP_ID_525808,Human_RBP_ID_769871,Human_RBP_ID_1017696,Human_RBP_ID_1570076 Human_Splice_Rec_2035476,Human_Splice_Rec_2035477,Human_Splice_Rec_2035526,Human_Splice_Rec_2035527,Human_Splice_Rec_2035578,Human_Splice_Rec_2035579,Human_Splice_Rec_2035632,Human_Splice_Rec_2035633,Human_Splice_Rec_2035686,Human_Splice_Rec_2035687,Human_Splice_Rec_2035732,Human_Splice_Rec_2035733,Human_Splice_Rec_2035784,Human_Splice_Rec_2035785,Human_Splice_Rec_2035840,Human_Splice_Rec_2035841 Clinvar_Rec_289,Clinvar_Rec_290 RMVar_hsa_circ_83318,RMVar_hsa_circ_100166,RMVar_hsa_circ_195998,RMVar_hsa_circ_195997,RMVar_hsa_circ_118447,RMVar_hsa_circ_75880,RMVar_hsa_circ_195999,RMVar_hsa_circ_196000 70474 RMVar_ID_70474 Human_SNP_ID_668632423 m1A Human chr19 + 50413520 50413520 50413520 CACAGTGGAGAATGGCTACAGCACCAGTGCCAAGGTCGGGGGCTGCCCACCGCTGCCCTGAGATG CACAGTGGAGAATGGCTACAGCACCAGTGCCAGGGTCGGGGGCTGCCCACCGCTGCCCTGAGATG A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50413484..50413568 26863196 MeRIP-seq:(Medium) rs771176744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955487,Human_RBP_ID_19094143 Human_Splice_Rec_2035480,Human_Splice_Rec_2035481,Human_Splice_Rec_2035530,Human_Splice_Rec_2035531,Human_Splice_Rec_2035582,Human_Splice_Rec_2035583,Human_Splice_Rec_2035636,Human_Splice_Rec_2035637,Human_Splice_Rec_2035692,Human_Splice_Rec_2035693,Human_Splice_Rec_2035736,Human_Splice_Rec_2035737,Human_Splice_Rec_2035788,Human_Splice_Rec_2035789,Human_Splice_Rec_2035844,Human_Splice_Rec_2035845,Human_Splice_Rec_2035849 RMVar_hsa_circ_100166,RMVar_hsa_circ_195997,RMVar_hsa_circ_46238,RMVar_hsa_circ_75880,RMVar_hsa_circ_195999,RMVar_hsa_circ_122704,RMVar_hsa_circ_196001 70475 RMVar_ID_70475 Human_SNP_ID_668632900 m1A Human chr19 + 50414933 50414933 50414933 CTGCAAGGGCCTGGAGGCCGTGCGCAGGGACAACTGCCCCCTCGTGGCCAACCTGGTCACTGCCT CTGCAAGGGCCTGGAGGCCGTGCGCAGGGACAGCTGCCCCCTCGTGGCCAACCTGGTCACTGCCT A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50414882..50415023 26863196 MeRIP-seq:(Medium) rs1555792872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8839487,Human_RBP_ID_9293901 Human_Splice_Rec_2035485,Human_Splice_Rec_2035535,Human_Splice_Rec_2035587,Human_Splice_Rec_2035641,Human_Splice_Rec_2035697,Human_Splice_Rec_2035741,Human_Splice_Rec_2035793,Human_Splice_Rec_2035853,Human_Splice_Rec_2035863 Clinvar_Rec_291 RMVar_hsa_circ_100166,RMVar_hsa_circ_195997,RMVar_hsa_circ_75880,RMVar_hsa_circ_195999,RMVar_hsa_circ_118404,RMVar_hsa_circ_114443,RMVar_hsa_circ_196002,RMVar_hsa_circ_196003 70476 RMVar_ID_70476 Human_SNP_ID_668633256 m1A Human chr19 + 50415707 50415707 50415707 CCCCGCCACCCACCTGCCCTCACCCACCCGCCACCCCATCTCCACGCAGGATGAGGAAGCGGGAC CCCCGCCACCCACCTGCCCTCACCCACCCGCCCCCCCATCTCCACGCAGGATGAGGAAGCGGGAC A C POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50415701..50415750 32194978 MeRIP-seq:(Medium) rs1158282465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118404,RMVar_hsa_circ_114443,RMVar_hsa_circ_196002,RMVar_hsa_circ_196003 70477 RMVar_ID_70477 Human_SNP_ID_668652954 m1A Human chr19 - 50476660 50476660 50476660 CCGCGCCCGCTATGCACAGCTAAAGAGCACTCACCCCTCGCGCACCAGTCCCGGCCCGGCAGCCG CCGCGCCCGCTATGCACAGCTAAAGAGCACTCTCCCCTCGCGCACCAGTCCCGGCCCGGCAGCCG T A FAM71E1 Ensembl:ENSG00000142530 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50476630..50476733 32194978 MeRIP-seq:(Medium) rs1277451291 Functional Loss SNV dbSNP153 33..33 33 - - - 70478 RMVar_ID_70478 Human_SNP_ID_668653632 m1A Human chr19 - 50478907 50478907 50478907 TCAGAGACGCCCCCTCCCCCGCCCACCCTTCAACCCAGGCAGGGGCCAGGAGGTCCAGCTTCAAA TCAGAGACGCCCCCTCCCCCGCCCACCCTTCAGCCCAGGCAGGGGCCAGGAGGTCCAGCTTCAAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50478905..50478992 26863196 MeRIP-seq:(Medium) rs775268079 Functional Loss SNV dbSNP153 33..33 33 - - - 70479 RMVar_ID_70479 Human_SNP_ID_668655106 m1A Human chr19 + 50482499 50482499 50482499 CTCCTGCGCCCGCCTCCCCCATGGCCCCATGCAGCCCCAGGGGCTTCCCCCCTGCCCATGGAGTA CTCCTGCGCCCGCCTCCCCCATGGCCCCATGCGGCCCCAGGGGCTTCCCCCCTGCCCATGGAGTA A G EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50482476..50482500 26863196 MeRIP-seq:(Medium) rs1216537529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240484,Human_RBP_ID_525835,Human_RBP_ID_5238877 Human_miRNA_ID_2437312,Human_miRNA_ID_2946378,Human_miRNA_ID_3004907 RMVar_hsa_circ_117118,RMVar_hsa_circ_127262,RMVar_hsa_circ_196005,RMVar_hsa_circ_127621,RMVar_hsa_circ_107325,RMVar_hsa_circ_196006,RMVar_hsa_circ_111762,RMVar_hsa_circ_196007,RMVar_hsa_circ_196008,RMVar_hsa_circ_196009 70480 RMVar_ID_70480 Human_SNP_ID_668655274 m1A Human chr19 - 50482985 50482985 50482985 GAGGGGGTTCTATTTACAGTGTCTGGGCTTTGACTCCACTAACTGTTGGTTTTGTTTTCTTTCTT GAGGGGGTTCTATTTACAGTGTCTGGGCTTTGCCTCCACTAACTGTTGGTTTTGTTTTCTTTCTT T G AC020909.3 Ensembl:ENSG00000268854 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50482934..50483087 26863196 MeRIP-seq:(Medium) rs1232452709 Functional Loss SNV dbSNP153 33..33 33 - - - 70481 RMVar_ID_70481 Human_SNP_ID_668656670 m1A Human chr19 - 50487708 50487708 50487708 TCCCTCCCGGGAGCCCCGTCTCCTCCGTCTCCAGGTGGCCCCTGCATCCCTGCCTGGTGGGCCTT TCCCTCCCGGGAGCCCCGTCTCCTCCGTCTCCGGGTGGCCCCTGCATCCCTGCCTGGTGGGCCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50487698..50487971 26863196 MeRIP-seq:(Medium) rs1231614244 Functional Loss SNV dbSNP153 33..33 33 - - - 70482 RMVar_ID_70482 Human_SNP_ID_668656998 m1A Human chr19 + 50488587 50488587 50488587 AGAGGGTGTTGGGGGAGAAGAGGGTGGGGGAGAGGGGGCCCCGGGAGAGGGAGGGATGGAGGAGC AGAGGGTGTTGGGGGAGAAGAGGGTGGGGGAGGGGGGGCCCCGGGAGAGGGAGGGATGGAGGAGC A G EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:50488564..50488693 26863196 MeRIP-seq:(Medium) rs975428780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264087,Human_RBP_ID_9427643 70483 RMVar_ID_70483 Human_SNP_ID_668657068 m1A Human chr19 + 50488839 50488839 50488839 AGGGAGAGAGGAGAGAGAAGAGCCGGACAGGGAGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACA AGGGAGAGAGGAGAGAGAAGAGCCGGACAGGGGGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACA A G EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50488670..50489170 26863196 MeRIP-seq:(Medium) rs1049738790 Functional Loss SNV dbSNP153 33..33 33 - - - 70484 RMVar_ID_70484 Human_SNP_ID_668657069 m1A Human chr19 + 50488839 50488839 50488839 AGGGAGAGAGGAGAGAGAAGAGCCGGACAGGGAGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACA AGGGAGAGAGGAGAGAGAAGAGCCGGACAGGGTGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACA A T EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50488670..50489170 26863196 MeRIP-seq:(Medium) rs1049738790 Functional Loss SNV dbSNP153 33..33 33 - - - 70485 RMVar_ID_70485 Human_SNP_ID_668657074 m1A Human chr19 + 50488871 50488870 50488872 AGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACAGAGAGGACAGCGAGAAAAAGAGAACAGGAAGA AGAGCAGAAGTGAGAAAAAGGAGGGTGGCCAC__AGAGGACAGCGAGAAAAAGAGAACAGGAAGA CAG C EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50488595..50488936 26863196 MeRIP-seq:(Medium) rs1413396034 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17068565 70486 RMVar_ID_70486 Human_SNP_ID_668657216 m1A Human chr19 + 50489335 50489334 50489336 TGAGTGAGCGAGAAAAAAAGCAGAAAGGAAAGAAGAGGTGCATGAGTGTGGAAGAGCAATATGGA TGAGTGAGCGAGAAAAAAAGCAGAAAGGAAAG__GAGGTGCATGAGTGTGGAAGAGCAATATGGA GAA G EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50489319..50489470 26863196 MeRIP-seq:(Medium) rs960737702 Functional Loss DEL dbSNP153 33..34 33 - - - 70487 RMVar_ID_70487 Human_SNP_ID_668657293 m1A Human chr19 + 50489685 50489681 50489685 CCACCCCGGGGCCATCTCTGTGACCCAGGGAGAGAAAGGACAACGAATGGGACTAGACGAGGATG CCACCCCGGGGCCATCTCTGTGACCCAGG____GAAAGGACAACGAATGGGACTAGACGAGGATG GGAGA G EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50489669..50489970 26863196 MeRIP-seq:(Medium) rs776417731 Functional Loss DEL dbSNP153 30..33 33 - - - 70488 RMVar_ID_70488 Human_SNP_ID_668657294 m1A Human chr19 + 50489685 50489685 50489685 CCACCCCGGGGCCATCTCTGTGACCCAGGGAGAGAAAGGACAACGAATGGGACTAGACGAGGATG CCACCCCGGGGCCATCTCTGTGACCCAGGGAGTGAAAGGACAACGAATGGGACTAGACGAGGATG A T EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50489669..50489970 26863196 MeRIP-seq:(Medium) rs550445236 Functional Loss SNV dbSNP153 33..33 33 - - - 70489 RMVar_ID_70489 Human_SNP_ID_668658007 m1A Human chr19 + 50491958 50491957 50491959 AGACAGCGAGAGAAACAGAGACAATGATGGCAAGAGAGTGAGAGAGACAGAGCGAGAGAGACAGA AGACAGCGAGAGAAACAGAGACAATGATGGCA__AGAGTGAGAGAGACAGAGCGAGAGAGACAGA AAG A lnc-EMC10-4,lnc-EMC10-4:2 RNACentral:URS00009B4BE6,RNACentral:URS00008BE6AA lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50491401..50492169 26863196 MeRIP-seq:(Medium) rs1437265671 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22975585 70490 RMVar_ID_70490 Human_SNP_ID_668659854 m1A Human chr19 + 50497646 50497646 50497646 TGGGGGAGAGACAGAGATAGAGGAAGTGGAGGAGAGACAGAGAGAAGTGGGGGAGAGACAGAGAC TGGGGGAGAGACAGAGATAGAGGAAGTGGAGGGGAGACAGAGAGAAGTGGGGGAGAGACAGAGAC A G lnc-EMC10-3,lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00008C2B78,RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:50497583..50497712 26863196 MeRIP-seq:(Medium) rs1466786168 Functional Loss SNV dbSNP153 33..33 33 - - - 70491 RMVar_ID_70491 Human_SNP_ID_668660810 m1A Human chr19 + 50499199 50499198 50499200 AGAGAGAGACAGAGGGAGACGGAGAGAGAGACAGGGAGAGAGAGAGACGGAGAGAGAGAGACAGA AGAGAGAGACAGAGGGAGACGGAGAGAGAGAC__GGAGAGAGAGAGACGGAGAGAGAGAGACAGA CAG C lnc-EMC10-3,lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00008C2B78,RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50498124..50499253 26863196 MeRIP-seq:(Medium) rs1479618986 Functional Loss DEL dbSNP153 33..34 33 - - - 70492 RMVar_ID_70492 Human_SNP_ID_668660816 m1A Human chr19 + 50499203 50499203 50499203 AGAGACAGAGGGAGACGGAGAGAGAGACAGGGAGAGAGAGAGACGGAGAGAGAGAGACAGAGGGA AGAGACAGAGGGAGACGGAGAGAGAGACAGGGGGAGAGAGAGACGGAGAGAGAGAGACAGAGGGA A G lnc-EMC10-3,lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00008C2B78,RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50498984..50499272 26863196 MeRIP-seq:(Medium) rs1276250685 Functional Loss SNV dbSNP153 33..33 33 - - - 70493 RMVar_ID_70493 Human_SNP_ID_668661001 m1A Human chr19 + 50499419 50499418 50499420 AGGGAGAGAGAGACAGAGAGAGAGAGGGAGACAGAGACGGAGAGAGAGACAGAGGGAGAGAGGGA AGGGAGAGAGAGACAGAGAGAGAGAGGGAGAC__AGACGGAGAGAGAGACAGAGGGAGAGAGGGA CAG C lnc-EMC10-3,lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00008C2B78,RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50499383..50500070 26863196 MeRIP-seq:(Medium) rs1284019663 Functional Loss DEL dbSNP153 33..34 33 - - - 70494 RMVar_ID_70494 Human_SNP_ID_668661211 m1A Human chr19 + 50499681 50499677 50499681 AGAGAGAGACAGAGGGAGAGAGAGAGACGGAGAGAGAGAGACGGAGAGAGAGACAGAGGGAGAGA AGAGAGAGACAGAGGGAGAGAGAGAGACG____GAGAGAGACGGAGAGAGAGACAGAGGGAGAGA GGAGA G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50499361..50500291 26863196 MeRIP-seq:(Medium) rs1330260933 Functional Loss DEL dbSNP153 30..33 33 - - - 70495 RMVar_ID_70495 Human_SNP_ID_668661212 m1A Human chr19 + 50499681 50499677 50499681 AGAGAGAGACAGAGGGAGAGAGAGAGACGGAGAGAGAGAGACGGAGAGAGAGACAGAGGGAGAGA AGAGAGAGACAGAGGGAGAGAGAGAGACGGA__GAGAGAGACGGAGAGAGAGACAGAGGGAGAGA GGAGA GGA lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50499361..50500291 26863196 MeRIP-seq:(Medium) rs1330260933 Functional Loss DEL dbSNP153 32..33 33 - - - 70496 RMVar_ID_70496 Human_SNP_ID_668661215 m1A Human chr19 + 50499681 50499681 50499681 AGAGAGAGACAGAGGGAGAGAGAGAGACGGAGAGAGAGAGACGGAGAGAGAGACAGAGGGAGAGA AGAGAGAGACAGAGGGAGAGAGAGAGACGGAGGGAGAGAGACGGAGAGAGAGACAGAGGGAGAGA A G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50499361..50500291 26863196 MeRIP-seq:(Medium) rs1254662785 Functional Loss SNV dbSNP153 33..33 33 - - - 70497 RMVar_ID_70497 Human_SNP_ID_668661256 m1A Human chr19 + 50499735 50499734 50499736 AGAGGGAGAGAGAGACAGAGAGAGGGAGAGAGAAGGAGAGAGAGAGAGAGGGAGAGAGAGACGGA AGAGGGAGAGAGAGACAGAGAGAGGGAGAGAG__GGAGAGAGAGAGAGAGGGAGAGAGAGACGGA GAA G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:50499448..50499859 26863196 MeRIP-seq:(Medium) rs1390994133 Functional Loss DEL dbSNP153 33..34 33 - - - 70498 RMVar_ID_70498 Human_SNP_ID_668661355 m1A Human chr19 + 50499853 50499850 50499854 AGGGAGAGAGAGAGACGGAGAGAGAGAGACAGAGGGAGACGGAGAGAGAGACGGAGAGAGAGAGA AGGGAGAGAGAGAGACGGAGAGAGAGAGAC____GGAGACGGAGAGAGAGACGGAGAGAGAGAGA CAGAG C lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50499847..50499931 26863196 MeRIP-seq:(Medium) rs751614408 Functional Loss DEL dbSNP153 31..34 33 - - - 70499 RMVar_ID_70499 Human_SNP_ID_668661359 m1A Human chr19 + 50499853 50499853 50499853 AGGGAGAGAGAGAGACGGAGAGAGAGAGACAGAGGGAGACGGAGAGAGAGACGGAGAGAGAGAGA AGGGAGAGAGAGAGACGGAGAGAGAGAGACAGGGGGAGACGGAGAGAGAGACGGAGAGAGAGAGA A G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50499847..50499931 26863196 MeRIP-seq:(Medium) rs1448814727 Functional Loss SNV dbSNP153 33..33 33 - - - 70500 RMVar_ID_70500 Human_SNP_ID_668661483 m1A Human chr19 + 50499999 50499998 50500000 GGAGAGAGAGACAGAGAGAGAGAGAGGGAGACAGAGACGGAGAGAGAGACAGAGGGAGAGAGGGA GGAGAGAGAGACAGAGAGAGAGAGAGGGAGAC__AGACGGAGAGAGAGACAGAGGGAGAGAGGGA CAG C lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50499992..50500137 26863196 MeRIP-seq:(Medium) rs1410023260 Functional Loss DEL dbSNP153 33..34 33 - - - 70501 RMVar_ID_70501 Human_SNP_ID_668661592 m1A Human chr19 + 50500163 50500160 50500164 AGAGGGAGAGAGGGAGACAGAGGGAGAGAGAGACAGGGAGAGAGGGAGACGGAGAGAGAGAGGGA AGAGGGAGAGAGGGAGACAGAGGGAGAGAG____AGGGAGAGAGGGAGACGGAGAGAGAGAGGGA GAGAC G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50500137..50500267 26863196 MeRIP-seq:(Medium) rs1175183689 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_17068422 70502 RMVar_ID_70502 Human_SNP_ID_668661877 m1A Human chr19 + 50501129 50501129 50501129 AAAGAGACAGAGAGGGGTGGAGAGAAATGCCCAGCAAGAGAGATAGAGAAGGGAGGCTGAGACAG AAAGAGACAGAGAGGGGTGGAGAGAAATGCCCGGCAAGAGAGATAGAGAAGGGAGGCTGAGACAG A G lnc-EMC10-4,lnc-EMC10-4:2,lnc-EMC10-4:3 RNACentral:URS00009B4BE6,RNACentral:URS00008B4477,RNACentral:URS00008BE6AA lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:50501123..50501228 26863196 MeRIP-seq:(Medium) rs1323438824 Functional Loss SNV dbSNP153 33..33 33 - - - 70503 RMVar_ID_70503 Human_SNP_ID_668663292 m1A Human chr19 + 50506225 50506225 50506225 TGCCCTTCTCCTCCACCTCCTTGGTCACTACCAGCAGCACCTCGCACAGGCCCTGGGCCAGCGCA TGCCCTTCTCCTCCACCTCCTTGGTCACTACCGGCAGCACCTCGCACAGGCCCTGGGCCAGCGCA A G lnc-EMC10-4 RNACentral:URS00009B4BE6 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50506046..50507641 32194978 MeRIP-seq:(Medium) rs755900464 Functional Loss SNV dbSNP153 33..33 33 - - - 70504 RMVar_ID_70504 Human_SNP_ID_668663364 m1A Human chr19 - 50506426 50506411 50506427 GCGCCAGGTGGACGGTGTCTACTACAACCTGGACTCCAAGCTGCGGGCGCCCGAGGCCCTGGGGG GCGCCAGGTGGACGGTGTCTACTACAACCTG________________CGCCCGAGGCCCTGGGGG GCCCGCAGCTTGGAGTC G JOSD2 Ensembl:ENSG00000161677 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:50506343..50506467;chr19:50506345..50506467 26863196 MeRIP-seq:(Medium) rs1568700384 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_525885 Human_Splice_Rec_2036145,Human_Splice_Rec_2036153,Human_Splice_Rec_2036159,Human_Splice_Rec_2036167 70505 RMVar_ID_70505 Human_SNP_ID_668663369 m1A Human chr19 - 50506426 50506426 50506426 GCGCCAGGTGGACGGTGTCTACTACAACCTGGACTCCAAGCTGCGGGCGCCCGAGGCCCTGGGGG GCGCCAGGTGGACGGTGTCTACTACAACCTGGCCTCCAAGCTGCGGGCGCCCGAGGCCCTGGGGG T G JOSD2 Ensembl:ENSG00000161677 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:50506343..50506467;chr19:50506345..50506467 26863196 MeRIP-seq:(Medium) rs750314091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525885 Human_Splice_Rec_2036145,Human_Splice_Rec_2036153,Human_Splice_Rec_2036159,Human_Splice_Rec_2036167 70506 RMVar_ID_70506 Human_SNP_ID_668664841 m1A Human chr19 + 50511041 50511041 50511041 CCTATCACCCAGCAACCAGGCCCCCTCCCCGGACACCAAGGAATGGAGCCCTTCGCCGACCCGCA CCTATCACCCAGCAACCAGGCCCCCTCCCCGGCCACCAAGGAATGGAGCCCTTCGCCGACCCGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50511036..50511326 26863196 MeRIP-seq:(Medium) rs1479790991 Functional Loss SNV dbSNP153 33..33 33 - - - 70507 RMVar_ID_70507 Human_SNP_ID_668665136 m1A Human chr19 + 50511735 50511735 50511735 ATCTTGTCTCGGGAGGGAGGAGGCTTCTCAGCAGAGATGGATCCCCGGCCTGGAGGGGAGCTGGC ATCTTGTCTCGGGAGGGAGGAGGCTTCTCAGCGGAGATGGATCCCCGGCCTGGAGGGGAGCTGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:50511698..50511811 26863196 MeRIP-seq:(Medium) rs1167928972 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70508 RMVar_ID_70508 Human_SNP_ID_668665251 m1A Human chr19 + 50512028 50512026 50512029 GAGGTTAAGGAAATAAAGGTCAGAAAGAAAGAAAGGTCAACAAATACAGAACCAGAACTGCAGAA GAGGTTAAGGAAATAAAGGTCAGAAAGAAAG___GGTCAACAAATACAGAACCAGAACTGCAGAA GAAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50511948..50512049 26863196 MeRIP-seq:(Medium) rs752167073 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13500267 70509 RMVar_ID_70509 Human_SNP_ID_668667267 m1A Human chr19 + 50517784 50517784 50517784 GCGGGCAGGGCCAGGTGGCTGTCCCCGCCCACACCACCCCCACTGGCCACGGCGGCCGCGGCGGC GCGGGCAGGGCCAGGTGGCTGTCCCCGCCCACGCCACCCCCACTGGCCACGGCGGCCGCGGCGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50517733..50518130 32194978 MeRIP-seq:(Medium) rs1047605506 Functional Loss SNV dbSNP153 33..33 33 - - - 70510 RMVar_ID_70510 Human_SNP_ID_668681704 m1A Human chr19 + 50568121 50568121 50568121 CGCTCTCCCCCCTCCCCGGCTCCTGGGTGGGGAGGGGGCTTCCGCAGCGGCGGCGGTGGGGCTGG CGCTCTCCCCCCTCCCCGGCTCCTGGGTGGGGGGGGGGCTTCCGCAGCGGCGGCGGTGGGGCTGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:50568024..50568221 26863410 MeRIP-seq:(Medium) rs929633267 Functional Loss SNV dbSNP153 33..33 33 - - - 70511 RMVar_ID_70511 Human_SNP_ID_668705961 m1A Human chr19 - 50658969 50658969 50658969 CCCGGAGCGCAGCAAGCGCGAGCGCGTCTGGAAGTCCGTGACCGCGATGAGCCACCTGTAAGGGG CCCGGAGCGCAGCAAGCGCGAGCGCGTCTGGAGGTCCGTGACCGCGATGAGCCACCTGTAAGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50658463..50659211 26863196 MeRIP-seq:(Medium) rs1170221127 Functional Loss SNV dbSNP153 33..33 33 - - - 70512 RMVar_ID_70512 Human_SNP_ID_668725198 m1A Human chr19 + 50723476 50723476 50723476 GCACTCGGCAGTTCCCAGAGGCCACCCCTCCCACCCCAGACATCCAGACATCTGGAACTTTGGGT GCACTCGGCAGTTCCCAGAGGCCACCCCTCCCGCCCCAGACATCCAGACATCTGGAACTTTGGGT A G CLEC11A Ensembl:ENSG00000105472 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:50723426..50723593 32194978 MeRIP-seq:(Medium) rs748910412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558696,Human_RBP_ID_27816651 70513 RMVar_ID_70513 Human_SNP_ID_668745106 m1A Human chr19 - 50791047 50791047 50791047 GAGTTGATGGAGGTCAGAGGTCGAGATGTGACAGGTTGAGATGGGGTCAGAAGTCAGTGTGGGTT GAGTTGATGGAGGTCAGAGGTCGAGATGTGACTGGTTGAGATGGGGTCAGAAGTCAGTGTGGGTT T A AC010325.1 Ensembl:ENSG00000261341 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50790934..50791177 26863196 MeRIP-seq:(Medium) rs1055740316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6780082,Human_RBP_ID_13500872 70514 RMVar_ID_70514 Human_SNP_ID_668746552 m1A Human chr19 - 50794875 50794875 50794875 GGGCCGGGGCAGTCAGCTGGTAGAAGCGGCCTAGTGGACAGGGGGCCGGGCACCCGGGGAGGCTG GGGCCGGGGCAGTCAGCTGGTAGAAGCGGCCTCGTGGACAGGGGGCCGGGCACCCGGGGAGGCTG T G lnc-C19orf48-5 RNACentral:URS0000D5C796 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50794824..50794917 26863196 MeRIP-seq:(Medium) rs780897905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13501012 70515 RMVar_ID_70515 Human_SNP_ID_668747842 m1A Human chr19 + 50798024 50798024 50798024 TCAGGGTGTGGCTAGCTCGACGGACACCGAACAGCTCCACAGGGAGGGTAGTGCCCAAGGCTTTT TCAGGGTGTGGCTAGCTCGACGGACACCGAACCGCTCCACAGGGAGGGTAGTGCCCAAGGCTTTT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:50797976..50798025 32194978 MeRIP-seq:(Medium) rs187835594 Functional Loss SNV dbSNP153 33..33 33 - - - 70516 RMVar_ID_70516 Human_SNP_ID_668747869 m1A Human chr19 - 50798085 50798085 50798085 TGGGGGAGCTGCTCCTGGTTTGAGCTGCATTCAGGAAGTGCGGGACATGGTAGGGGAGGCAAAAA TGGGGGAGCTGCTCCTGGTTTGAGCTGCATTCGGGAAGTGCGGGACATGGTAGGGGAGGCAAAAA T C C19orf48 Ensembl:ENSG00000167747 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1225114206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_525921,Human_RBP_ID_1570182,Human_RBP_ID_1891204,Human_RBP_ID_2569151,Human_RBP_ID_3575492,Human_RBP_ID_4559841,Human_RBP_ID_5116403,Human_RBP_ID_6780167,Human_RBP_ID_8492712,Human_RBP_ID_13501145,Human_RBP_ID_18166113,Human_RBP_ID_18738188,Human_RBP_ID_20414797,Human_RBP_ID_25431521,Human_RBP_ID_26469900,Human_RBP_ID_26817926 RMVar_hsa_circ_95887,RMVar_hsa_circ_121058,RMVar_hsa_circ_196018,RMVar_hsa_circ_89603,RMVar_hsa_circ_196019,RMVar_hsa_circ_196017 70517 RMVar_ID_70517 Human_SNP_ID_668747965 m1A Human chr19 - 50798248 50798248 50798248 CCAAGGGCTTCCTGCAGGCTAGGGGAGGAGCCACCCCCGCTTCCCTATTGTGACCAGGCCTATGG CCAAGGGCTTCCTGCAGGCTAGGGGAGGAGCCGCCCCCGCTTCCCTATTGTGACCAGGCCTATGG T C C19orf48 Ensembl:ENSG00000167747 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50798110..50798344 26863196 MeRIP-seq:(Medium) rs1293132318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54471,Human_RBP_ID_264092,Human_RBP_ID_525933,Human_RBP_ID_5116404,Human_RBP_ID_8492715,Human_RBP_ID_18193193,Human_RBP_ID_22070493,Human_RBP_ID_26472853,Human_RBP_ID_26994447,Human_RBP_ID_27277577,Human_RBP_ID_27470726 RMVar_hsa_circ_3479,RMVar_hsa_circ_95887,RMVar_hsa_circ_121058,RMVar_hsa_circ_196018,RMVar_hsa_circ_89603,RMVar_hsa_circ_196019,RMVar_hsa_circ_196017 70518 RMVar_ID_70518 Human_SNP_ID_668750048 m1A Human chr19 + 50803971 50803971 50803971 CAGGTAAGCAAAGGCCTCGTTTGCTTCCTTCTATATCCATTCCTACACGACTCTCAAACCCGGCA CAGGTAAGCAAAGGCCTCGTTTGCTTCCTTCTGTATCCATTCCTACACGACTCTCAAACCCGGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50803967..50804066 26863196 MeRIP-seq:(Medium) rs974782259 Functional Loss SNV dbSNP153 33..33 33 - - - 70519 RMVar_ID_70519 Human_SNP_ID_668836105 m1A Human chr19 - 51104187 51104187 51104187 CTACGAAGACCTCTTTGGGGGCTGGACGATGGACGCCGTGGCCCGCAGCACAGCCGGCTCCGGCC CTACGAAGACCTCTTTGGGGGCTGGACGATGGGCGCCGTGGCCCGCAGCACAGCCGGCTCCGGCC T C CTU1 Ensembl:ENSG00000142544 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:51104155..51104282 26863196 MeRIP-seq:(Medium) rs1215239366 Functional Loss SNV dbSNP153 33..33 33 - - - 70520 RMVar_ID_70520 Human_SNP_ID_668836279 m1A Human chr19 - 51104589 51104587 51104590 TGTAACCCACCTCCTCTCTCTCCCTGTCTAGGAGAAGCCGACCCCTCCCGCAATGCCCGCCCCGC TGTAACCCACCTCCTCTCTCTCCCTGTCTAG___AAGCCGACCCCTCCCGCAATGCCCGCCCCGC TCTC T CTU1 Ensembl:ENSG00000142544 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:51104440..51104588 26863196 MeRIP-seq:(Medium) rs1158673677 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_241705,Human_RBP_ID_4558704,Human_RBP_ID_9329164 Human_Splice_Rec_2037572 70521 RMVar_ID_70521 Human_SNP_ID_668895596 m1A Human chr19 - 51345365 51345362 51345365 GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGAAGATCGAGGTGATCAAGCCTGGGGACCTGGGTG GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGA___TCGAGGTGATCAAGCCTGGGGACCTGGGTG ATCT A ETFB Ensembl:ENSG00000105379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51345237..51345440 26863196 MeRIP-seq:(Medium) rs767519060 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_17656339,Human_RBP_ID_18738281,Human_RBP_ID_18998656,Human_RBP_ID_22447974,Human_RBP_ID_22763127,Human_RBP_ID_26336676 Human_Splice_Rec_2037910,Human_Splice_Rec_2037920,Human_Splice_Rec_2037928 70522 RMVar_ID_70522 Human_SNP_ID_668895597 m1A Human chr19 - 51345365 51345365 51345365 GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGAAGATCGAGGTGATCAAGCCTGGGGACCTGGGTG GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGATGATCGAGGTGATCAAGCCTGGGGACCTGGGTG T A ETFB Ensembl:ENSG00000105379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51345237..51345440 26863196 MeRIP-seq:(Medium) rs1439090803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17656339,Human_RBP_ID_18738281,Human_RBP_ID_18998656,Human_RBP_ID_22447974,Human_RBP_ID_22763127,Human_RBP_ID_26336676 Human_Splice_Rec_2037910,Human_Splice_Rec_2037920,Human_Splice_Rec_2037928 70523 RMVar_ID_70523 Human_SNP_ID_668896073 m1A Human chr19 - 51346970 51346970 51346970 GATCGATGGGGGCCTGGAGACCCTGCGCCTGAAGCTGCCAGCTGTGGTGACAGCTGACCTGAGGC GATCGATGGGGGCCTGGAGACCCTGCGCCTGAGGCTGCCAGCTGTGGTGACAGCTGACCTGAGGC T C ETFB Ensembl:ENSG00000105379 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:51346968..51347119 26863410 MeRIP-seq:(Medium) rs1036677852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773231,Human_RBP_ID_4572479,Human_RBP_ID_8840209,Human_RBP_ID_9330235,Human_RBP_ID_9381338,Human_RBP_ID_17656340,Human_RBP_ID_17935520,Human_RBP_ID_18470654,Human_RBP_ID_22446988,Human_RBP_ID_26334954 Human_Splice_Rec_2037908,Human_Splice_Rec_2037909,Human_Splice_Rec_2037918,Human_Splice_Rec_2037919,Human_Splice_Rec_2037926,Human_Splice_Rec_2037927 70524 RMVar_ID_70524 Human_SNP_ID_668896074 m1A Human chr19 - 51346970 51346970 51346970 GATCGATGGGGGCCTGGAGACCCTGCGCCTGAAGCTGCCAGCTGTGGTGACAGCTGACCTGAGGC GATCGATGGGGGCCTGGAGACCCTGCGCCTGACGCTGCCAGCTGTGGTGACAGCTGACCTGAGGC T G ETFB Ensembl:ENSG00000105379 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:51346968..51347119 26863410 MeRIP-seq:(Medium) rs1036677852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773231,Human_RBP_ID_4572479,Human_RBP_ID_8840209,Human_RBP_ID_9330235,Human_RBP_ID_9381338,Human_RBP_ID_17656340,Human_RBP_ID_17935520,Human_RBP_ID_18470654,Human_RBP_ID_22446988,Human_RBP_ID_26334954 Human_Splice_Rec_2037908,Human_Splice_Rec_2037909,Human_Splice_Rec_2037918,Human_Splice_Rec_2037919,Human_Splice_Rec_2037926,Human_Splice_Rec_2037927 70525 RMVar_ID_70525 Human_SNP_ID_668896098 m1A Human chr19 + 51347012 51347012 51347012 GGGTCTCCAGGCCCCCATCGATCTCCCGCTCCACTTTCAACTTGTCCCCCTCCAGCGTCACCTGG GGGTCTCCAGGCCCCCATCGATCTCCCGCTCCGCTTTCAACTTGTCCCCCTCCAGCGTCACCTGG A G AC008750.4 Ensembl:ENSG00000267984 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:51346853..51347098;chr19:51346862..51347093;chr19:51346851..51347100 26863196 MeRIP-seq:(Medium) rs141774128 Functional Loss SNV dbSNP153 33..33 33 - - - 70526 RMVar_ID_70526 Human_SNP_ID_668898071 m1A Human chr19 - 51354250 51354250 51354250 TGTGGTCACGGATGGTGTGAAGCACTCCATGAACCCCTTCTGTGAGATCGCGGTGGAGGAGGCTG TGTGGTCACGGATGGTGTGAAGCACTCCATGATCCCCTTCTGTGAGATCGCGGTGGAGGAGGCTG T A ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding CDS,3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1473834913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139687,Human_RBP_ID_1570276,Human_RBP_ID_1891240,Human_RBP_ID_4544724,Human_RBP_ID_9293913,Human_RBP_ID_9329167,Human_RBP_ID_9381344,Human_RBP_ID_17929971,Human_RBP_ID_18998662,Human_RBP_ID_22448989,Human_RBP_ID_23211029,Human_RBP_ID_23805602,Human_RBP_ID_26336680 Human_Splice_Rec_2037912,Human_Splice_Rec_2037922,Human_Splice_Rec_2037930,Human_Splice_Rec_2037936 RMVar_hsa_circ_74163,RMVar_hsa_circ_317800 70527 RMVar_ID_70527 Human_SNP_ID_668898103 m1A Human chr19 - 51354310 51354310 51354310 TCCTGACCCCACCCCTTCCCCTCCTGCTGGGCAGATCCGAGTGAAGCCTGACAGGACCGGTGTGG TCCTGACCCCACCCCTTCCCCTCCTGCTGGGCGGATCCGAGTGAAGCCTGACAGGACCGGTGTGG T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding CDS,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:51354226..51354364 26863410 MeRIP-seq:(Medium) rs1189473901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4544730,Human_RBP_ID_9293913,Human_RBP_ID_9329167,Human_RBP_ID_22071703,Human_RBP_ID_22448990,Human_RBP_ID_22663135 70528 RMVar_ID_70528 Human_SNP_ID_668901194 m1A Human chr19 + 51366310 51366310 51366310 CGTAGTCGATGACCCTCTTGACAGCTACGAGCACGCGCAGCTCCGCCATCTTCCCGCCGCAGCCA CGTAGTCGATGACCCTCTTGACAGCTACGAGCGCGCGCAGCTCCGCCATCTTCCCGCCGCAGCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:51354093..51368474 26863196 MeRIP-seq:(Medium) rs1227484897 Functional Loss SNV dbSNP153 33..33 33 - - - 70529 RMVar_ID_70529 Human_SNP_ID_668901623 m1A Human chr19 + 51367422 51367410 51367422 TGGGGAGCCTCTGGGGTGAGGGTCTTCTGGGCAGTCTCCTCCACCCTCTTCCCGCTGTCCAGTTT TGGGGAGCCTCTGGGGTGAGG____________GTCTCCTCCACCCTCTTCCCGCTGTCCAGTTT GGTCTTCTGGGCA G NONHSAG026361.2 RNACentral:URS00008BCD1C lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:51367391..51367491 32194978 MeRIP-seq:(Medium) rs1032144137 Functional Loss DEL dbSNP153 22..33 33 - - - 70530 RMVar_ID_70530 Human_SNP_ID_668956795 m1A Human chr19 - 51571321 51571320 51571321 ATTCCCAATCACTTCAGCGTCCAGTAAGCGACATAGGCTTAGATCCACTTAACAACAGAAGCTAA ATTCCCAATCACTTCAGCGTCCAGTAAGCGAC_TAGGCTTAGATCCACTTAACAACAGAAGCTAA AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:51571307..51571445 26863196 MeRIP-seq:(Medium) rs1568571155 Functional Loss DEL dbSNP153 33..33 33 - - - 70531 RMVar_ID_70531 Human_SNP_ID_668965158 m1A Human chr19 + 51601617 51601617 51601617 TGAACCGCGGTCGGCCCCGCCTGGCCATCGGCAAGGGCCGCCGGGGGCTGGACGAGGAGGCGACG TGAACCGCGGTCGGCCCCGCCTGGCCATCGGCGAGGGCCGCCGGGGGCTGGACGAGGAGGCGACG A G AC018755.3 Ensembl:ENSG00000269388 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:51601329..51601723 32194978 MeRIP-seq:(Medium) rs1200579071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17667781 70532 RMVar_ID_70532 Human_SNP_ID_668987870 m1A Human chr19 + 51688798 51688798 51688798 AAAGAGGATGGAGATAGGGAGAGGGCGAAAGGAAGGACAGATGTGCAGAGACAGAAGGGAGGACA AAAGAGGATGGAGATAGGGAGAGGGCGAAAGGTAGGACAGATGTGCAGAGACAGAAGGGAGGACA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51688785..51688977 26863196 MeRIP-seq:(Medium) rs1437779911 Functional Loss SNV dbSNP153 33..33 33 - - - 70533 RMVar_ID_70533 Human_SNP_ID_668987878 m1A Human chr19 + 51688837 51688834 51688838 GATGTGCAGAGACAGAAGGGAGGACAGACGGAAAGAGACACAGAGAGGCAGCAAAAGCAACCAAG GATGTGCAGAGACAGAAGGGAGGACAGACG____GAGACACAGAGAGGCAGCAAAAGCAACCAAG GGAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:51688605..51689057;chr19:51688661..51689014 26863196 MeRIP-seq:(Medium) rs1239698686 Functional Loss DEL dbSNP153 31..34 33 - - - 70534 RMVar_ID_70534 Human_SNP_ID_668988163 m1A Human chr19 + 51689431 51689431 51689431 GACGGCCGGAGGGAGTCGGGGAGAAGGGAAGGAGGATGGCGGGGACGGCGGGAGGAAGGGGAGAG GACGGCCGGAGGGAGTCGGGGAGAAGGGAAGGCGGATGGCGGGGACGGCGGGAGGAAGGGGAGAG A C SPACA6 Ensembl:ENSG00000182310 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:51689303..51689562 26863196 MeRIP-seq:(Medium) rs1039326707 Functional Loss SNV dbSNP153 33..33 33 - - - 70535 RMVar_ID_70535 Human_SNP_ID_668988172 m1A Human chr19 + 51689451 51689448 51689451 GAGAAGGGAAGGAGGATGGCGGGGACGGCGGGAGGAAGGGGAGAGGCCGCCGTGCGGCGAAGGCG GAGAAGGGAAGGAGGATGGCGGGGACGGCG___GGAAGGGGAGAGGCCGCCGTGCGGCGAAGGCG GGGA G SPACA6 Ensembl:ENSG00000182310 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51689311..51689650 26863196 MeRIP-seq:(Medium) rs1321215169 Functional Loss DEL dbSNP153 31..33 33 - - - 70536 RMVar_ID_70536 Human_SNP_ID_668988429 m1A Human chr19 + 51690325 51690325 51690325 GCCCCTAACTCCTTCAAAACCCCAGAGTTCAGAACCTCAGCCCCTCTTCCCAAGGAGCGCGGCCC GCCCCTAACTCCTTCAAAACCCCAGAGTTCAGCACCTCAGCCCCTCTTCCCAAGGAGCGCGGCCC A C SPACA6 Ensembl:ENSG00000182310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51690315..51690609 26863196 MeRIP-seq:(Medium) rs899026471 Functional Loss SNV dbSNP153 33..33 33 - - - 70537 RMVar_ID_70537 Human_SNP_ID_668989423 m1A Human chr19 - 51693382 51693382 51693382 TGTCATGCTCTGGAGGAAGGGTATGAGGAGTCAGGGGTCAGAAGTCAGGCCAGCAATTCCCCAGG TGTCATGCTCTGGAGGAAGGGTATGAGGAGTCTGGGGTCAGAAGTCAGGCCAGCAATTCCCCAGG T A SPACA6P-AS Ensembl:ENSG00000269959 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:51693372..51693712 26863196 MeRIP-seq:(Medium) rs760430790 Functional Loss SNV dbSNP153 33..33 33 - - - 70538 RMVar_ID_70538 Human_SNP_ID_668990207 m1A Human chr19 - 51696191 51696191 51696191 CCTCCAGACTCTCCCTCTGGTCCATCTTTGACACGACCCCAGAGGGTTCTTTCTACACCCAGAGC CCTCCAGACTCTCCCTCTGGTCCATCTTTGACCCGACCCCAGAGGGTTCTTTCTACACCCAGAGC T G lnc-HAS1-2,lnc-HAS1-2:2 RNACentral:URS0000D5D289,RNACentral:URS0000D587CB lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:51696186..51696296 26863196 MeRIP-seq:(Medium) rs939564737 Functional Loss SNV dbSNP153 33..33 33 - - - 70539 RMVar_ID_70539 Human_SNP_ID_668991701 m1A Human chr19 + 51702750 51702750 51702750 ACATCAAGTGTGGGAAAGCGGGTGGGCTTCACATCCTTAGGAAGCCAATAAGATCCCTGGAGAAA ACATCAAGTGTGGGAAAGCGGGTGGGCTTCACTTCCTTAGGAAGCCAATAAGATCCCTGGAGAAA A T SPACA6 Ensembl:ENSG00000182310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:51702725..51702872;chr19:51702701..51702842 26863196 MeRIP-seq:(Medium) rs1456642031 Functional Loss SNV dbSNP153 33..33 33 - - - 70540 RMVar_ID_70540 Human_SNP_ID_669061785 m1A Human chr19 + 51986609 51986609 51986609 GCGGACCACAGACAGGGGGATCACAGACTCCCACCAGGTACCTCCCAAATGCCTATACCCCGGCG GCGGACCACAGACAGGGGGATCACAGACTCCCTCCAGGTACCTCCCAAATGCCTATACCCCGGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:51986600..51986672 26863196 MeRIP-seq:(Medium) rs761673654 Functional Loss SNV dbSNP153 33..33 33 - - - 70541 RMVar_ID_70541 Human_SNP_ID_669061846 m1A Human chr19 - 51986801 51986801 51986801 AAGTAGGAGCAGTTTACGGAAGTGTAACGTTGAGGCCCTTCTTGTGTATCTGGAGAAAATAGAGG AAGTAGGAGCAGTTTACGGAAGTGTAACGTTGGGGCCCTTCTTGTGTATCTGGAGAAAATAGAGG T C ZNF350 Ensembl:ENSG00000256683 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:51986735..51986823 26863196 MeRIP-seq:(Medium) rs1482558374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2038859,Human_Splice_Rec_2038867,Human_Splice_Rec_2038875,Human_Splice_Rec_2038883,Human_Splice_Rec_2038889,Human_Splice_Rec_2038909,Human_Splice_Rec_2038911 RMVar_hsa_circ_119080,RMVar_hsa_circ_196055 70542 RMVar_ID_70542 Human_SNP_ID_669077635 m1A Human chr19 - 52048741 52048741 52048741 CGAGGGGCCCAGAAGTGGAAGAAGTTTAGGGAAGTAAGTTCAGCTTTTAAGAGGTCGCGGCGATT CGAGGGGCCCAGAAGTGGAAGAAGTTTAGGGAGGTAAGTTCAGCTTTTAAGAGGTCGCGGCGATT T C ZNF432 Ensembl:ENSG00000256087 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52048677..52048812 26863196 MeRIP-seq:(Medium) rs1026734495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2039067,Human_Splice_Rec_2039099 70543 RMVar_ID_70543 Human_SNP_ID_669077650 m1A Human chr19 + 52048777 52048777 52048777 CTAAACTTCTTCCACTTCTGGGCCCCTCGCCCAACTCCCTCCCCCTCTAAACCTCCAGAGACGGT CTAAACTTCTTCCACTTCTGGGCCCCTCGCCCGACTCCCTCCCCCTCTAAACCTCCAGAGACGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52048633..52048907 26863196 MeRIP-seq:(Medium) rs554633387 Functional Loss SNV dbSNP153 33..33 33 - - - 70544 RMVar_ID_70544 Human_SNP_ID_669089184 m1A Human chr19 - 52095695 52095694 52095695 GCTATGAGTGTGTTTCAGTCTACCTGGATTAAACGTTTGCTTCTCTTCGTCTACCTTGATTAAAC GCTATGAGTGTGTTTCAGTCTACCTGGATTAA_CGTTTGCTTCTCTTCGTCTACCTTGATTAAAC GT G ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52095601..52095731 26863196 MeRIP-seq:(Medium) rs890857597 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9381354,Human_RBP_ID_26336697 RMVar_hsa_circ_106922,RMVar_hsa_circ_196064,RMVar_hsa_circ_82429,RMVar_hsa_circ_100334,RMVar_hsa_circ_196074,RMVar_hsa_circ_196075,RMVar_hsa_circ_196077 70545 RMVar_ID_70545 Human_SNP_ID_669100948 m1A Human chr19 + 52143209 52143209 52143209 AAAGTATAACTGGAGTGCCAAGGCTAAAAGACAAAATACCACCGGAACTGGTGGAATGAGGCACC AAAGTATAACTGGAGTGCCAAGGCTAAAAGACGAAATACCACCGGAACTGGTGGAATGAGGCACC A G AC011468.3,RPL37P23 Ensembl:ENSG00000268458,Ensembl:ENSG00000243680 lincRNA,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs756302885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26475143 Human_miRNA_ID_1877777 70546 RMVar_ID_70546 Human_SNP_ID_669108111 m1A Human chr19 + 52171549 52171549 52171549 TTCCGGGTGTGCAGGAAGCTACACGCCCTGAGAAAAAAGACTGAGAGACCTGGGGCGGGAGAGGG TTCCGGGTGTGCAGGAAGCTACACGCCCTGAGGAAAAAGACTGAGAGACCTGGGGCGGGAGAGGG A G AC010320.2 Ensembl:ENSG00000267927 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52171528..52171610 26863196 MeRIP-seq:(Medium) rs1358839132 Functional Loss SNV dbSNP153 33..33 33 - - - 70547 RMVar_ID_70547 Human_SNP_ID_669113468 m1A Human chr19 - 52190409 52190409 52190409 AACCTCCCAGGACCGCGGACCGCCGCGCGCACAGGGCAGGCCCGGGACCCTCGAGGCTAGCGCTG AACCTCCCAGGACCGCGGACCGCCGCGCGCACTGGGCAGGCCCGGGACCCTCGAGGCTAGCGCTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52190406..52190534 26863196 MeRIP-seq:(Medium) rs1364079926 Functional Loss SNV dbSNP153 33..33 33 - - - 70548 RMVar_ID_70548 Human_SNP_ID_669113469 m1A Human chr19 - 52190409 52190409 52190409 AACCTCCCAGGACCGCGGACCGCCGCGCGCACAGGGCAGGCCCGGGACCCTCGAGGCTAGCGCTG AACCTCCCAGGACCGCGGACCGCCGCGCGCACCGGGCAGGCCCGGGACCCTCGAGGCTAGCGCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52190406..52190534 26863196 MeRIP-seq:(Medium) rs1364079926 Functional Loss SNV dbSNP153 33..33 33 - - - 70549 RMVar_ID_70549 Human_SNP_ID_669122830 m1A Human chr19 + 52226152 52226152 52226152 TTCCTCCTCTCCCCAGCCTGGGAAGATGTCTCACTGTCCACCTCCCAACGGGCTAGGGGAGCACG TTCCTCCTCTCCCCAGCCTGGGAAGATGTCTCGCTGTCCACCTCCCAACGGGCTAGGGGAGCACG A G PPP2R1A Ensembl:ENSG00000105568 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52225947..52226352 26863196 MeRIP-seq:(Medium) rs1471618111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526282,Human_RBP_ID_3575822,Human_RBP_ID_5116406,Human_RBP_ID_6781592,Human_RBP_ID_9292691,Human_RBP_ID_17270457,Human_RBP_ID_17387042,Human_RBP_ID_17656343,Human_RBP_ID_17930321,Human_RBP_ID_18738546,Human_RBP_ID_23806039,Human_RBP_ID_24484795,Human_RBP_ID_26469998,Human_RBP_ID_26994749,Human_RBP_ID_27277798 RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_127662,RMVar_hsa_circ_97176,RMVar_hsa_circ_196084,RMVar_hsa_circ_122127,RMVar_hsa_circ_196093,RMVar_hsa_circ_122250,RMVar_hsa_circ_196094,RMVar_hsa_circ_196096,RMVar_hsa_circ_105564,RMVar_hsa_circ_126910,RMVar_hsa_circ_77928,RMVar_hsa_circ_196104,RMVar_hsa_circ_196106,RMVar_hsa_circ_196109,RMVar_hsa_circ_112824,RMVar_hsa_circ_196111 70550 RMVar_ID_70550 Human_SNP_ID_669122886 m1A Human chr19 - 52226341 52226341 52226341 GAATAAAATAAAAACGGCACAGTTGACACACAAAAAAAAACCAATGATGGGGAGGACGGGAGGTG GAATAAAATAAAAACGGCACAGTTGACACACACAAAAAAACCAATGATGGGGAGGACGGGAGGTG T G AC010320.3 Ensembl:ENSG00000268015 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:52226251..52226400 26863196 MeRIP-seq:(Medium) rs80257415 Functional Loss SNV dbSNP153 33..33 33 - - - 70551 RMVar_ID_70551 Human_SNP_ID_669133224 m1A Human chr19 + 52269622 52269622 52269622 CCCGGAAGTGGATGGCGTGGAGATATGGCGCAACTGCGGCGCGTGAGTTTTCCTTTGTTTAGATT CCCGGAAGTGGATGGCGTGGAGATATGGCGCAGCTGCGGCGCGTGAGTTTTCCTTTGTTTAGATT A G ZNF766 Ensembl:ENSG00000196214 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52269613..52269680 26863196 MeRIP-seq:(Medium) rs553709500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2039359,Human_Splice_Rec_2039363,Human_Splice_Rec_2039369,Human_Splice_Rec_2039375 70552 RMVar_ID_70552 Human_SNP_ID_669133472 m1A Human chr19 + 52270303 52270303 52270303 GAGCGAGGTAGAGGAAACAGAAAAATTTAGAGAGAAAATAATGAGGAAGATCCATAACAAGACGG GAGCGAGGTAGAGGAAACAGAAAAATTTAGAGGGAAAATAATGAGGAAGATCCATAACAAGACGG A G ZNF766 Ensembl:ENSG00000196214 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52270289..52270373 26863196 MeRIP-seq:(Medium) rs996573366 Functional Loss SNV dbSNP153 33..33 33 - - - 70553 RMVar_ID_70553 Human_SNP_ID_669133475 m1A Human chr19 - 52270309 52270306 52270309 GCGTTGCCGTCTTGTTATGGATCTTCCTCATTATTTTCTCTCTAAATTTTTCTGTTTCCTCTACC GCGTTGCCGTCTTGTTATGGATCTTCCTCATT___TTCTCTCTAAATTTTTCTGTTTCCTCTACC AAAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52270294..52270807 26863196 MeRIP-seq:(Medium) rs1335163852 Functional Loss DEL dbSNP153 33..35 33 - - - 70554 RMVar_ID_70554 Human_SNP_ID_669141733 m1A Human chr19 + 52298614 52298612 52298614 GATTGCGCCATTGCACTCCAGGCTGGGCGACAAGAGCAAAACTCCGTCTCAGGGAAAAAAAAAAA GATTGCGCCATTGCACTCCAGGCTGGGCGAC__GAGCAAAACTCCGTCTCAGGGAAAAAAAAAAA CAA C ZNF480 Ensembl:ENSG00000198464 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52298608..52298950 26863196 MeRIP-seq:(Medium) rs1256748951 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_93839,RMVar_hsa_circ_196116 70555 RMVar_ID_70555 Human_SNP_ID_669141735 m1A Human chr19 + 52298614 52298614 52298614 GATTGCGCCATTGCACTCCAGGCTGGGCGACAAGAGCAAAACTCCGTCTCAGGGAAAAAAAAAAA GATTGCGCCATTGCACTCCAGGCTGGGCGACAGGAGCAAAACTCCGTCTCAGGGAAAAAAAAAAA A G ZNF480 Ensembl:ENSG00000198464 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52298608..52298950 26863196 MeRIP-seq:(Medium) rs1290164556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93839,RMVar_hsa_circ_196116 70556 RMVar_ID_70556 Human_SNP_ID_669206671 m1A Human chr19 + 52528745 52528745 52528745 ACAGCAGGGAGGACACCTGGGGATCTGGGGTGACACAGAGTGGGGACAGGGGAGTATATCAGGGA ACAGCAGGGAGGACACCTGGGGATCTGGGGTGCCACAGAGTGGGGACAGGGGAGTATATCAGGGA A C ZNF808 Ensembl:ENSG00000198482 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52528741..52528837 26863196 MeRIP-seq:(Medium) rs138714743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196156,RMVar_hsa_circ_107441,RMVar_hsa_circ_196155 70557 RMVar_ID_70557 Human_SNP_ID_669206702 m1A Human chr19 - 52528821 52528821 52528821 CGTCCTCAATCTCCATCTATTTCTGCCTCTTCACCCATCTCTGCGCCTCCTCTGCTCTCCCTGTT CGTCCTCAATCTCCATCTATTTCTGCCTCTTCTCCCATCTCTGCGCCTCCTCTGCTCTCCCTGTT T A HSALNG0127327 RNACentral:URS0000EA207E lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52528803..52528973 26863196 MeRIP-seq:(Medium) rs368012957 Functional Loss SNV dbSNP153 33..33 33 - - - 70558 RMVar_ID_70558 Human_SNP_ID_669206703 m1A Human chr19 - 52528821 52528821 52528821 CGTCCTCAATCTCCATCTATTTCTGCCTCTTCACCCATCTCTGCGCCTCCTCTGCTCTCCCTGTT CGTCCTCAATCTCCATCTATTTCTGCCTCTTCGCCCATCTCTGCGCCTCCTCTGCTCTCCCTGTT T C HSALNG0127327 RNACentral:URS0000EA207E lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52528803..52528973 26863196 MeRIP-seq:(Medium) rs368012957 Functional Loss SNV dbSNP153 33..33 33 - - - 70559 RMVar_ID_70559 Human_SNP_ID_669228552 m1A Human chr19 + 52598491 52598491 52598491 GGAGTGGCGCGCTGGTTGCCGCGGGCACTGGCAATTAGAAGGGATTATTAAACTAAGCAAGGTCC GGAGTGGCGCGCTGGTTGCCGCGGGCACTGGCGATTAGAAGGGATTATTAAACTAAGCAAGGTCC A G lnc-ZNF701-1,lnc-ZNF701-1:2 RNACentral:URS00008B80E1,RNACentral:URS0000D5C466 lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52598422..52598519 26863196 MeRIP-seq:(Medium) rs1375808731 Functional Loss SNV dbSNP153 33..33 33 - - - 70560 RMVar_ID_70560 Human_SNP_ID_669236718 m1A Human chr19 - 52624852 52624852 52624852 GGAGCAAAAAGTATATGCATCAGGTGTGAGGAAGAAAATAGATTTGGGAAGTTATGAGAAATGTG GGAGCAAAAAGTATATGCATCAGGTGTGAGGAGGAAAATAGATTTGGGAAGTTATGAGAAATGTG T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52624831..52625000 26863196 MeRIP-seq:(Medium) rs1358053351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9817,RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_309270,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281,RMVar_hsa_circ_42184 70561 RMVar_ID_70561 Human_SNP_ID_669240448 m1A Human chr19 - 52637032 52637031 52637033 AGCAGAATGCCAGGTAAAAAGAAAAGAAAACAAGAGCTAGAGAGAGAAGGGGAGAATGAGAGATA AGCAGAATGCCAGGTAAAAAGAAAAGAAAAC__GAGCTAGAGAGAGAAGGGGAGAATGAGAGATA CTT C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52636961..52637318 26863196 MeRIP-seq:(Medium) rs990987743 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 70562 RMVar_ID_70562 Human_SNP_ID_669240457 m1A Human chr19 + 52637050 52637050 52637050 TCTCTCTCTAGCTCTTGTTTTCTTTTCTTTTTACCTGGCATTCTGCTCCTCATTTTGTACCCCTC TCTCTCTCTAGCTCTTGTTTTCTTTTCTTTTTCCCTGGCATTCTGCTCCTCATTTTGTACCCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52637049..52637222 26863196 MeRIP-seq:(Medium) rs1014195309 Functional Loss SNV dbSNP153 33..33 33 - - - 70563 RMVar_ID_70563 Human_SNP_ID_669240598 m1A Human chr19 - 52637456 52637456 52637456 AAACCTAGATGTACAGAGAGATGAAGGACAGCAAGGTAGGGAGAGGGGCAGCAAAGAGGGAATCT AAACCTAGATGTACAGAGAGATGAAGGACAGCGAGGTAGGGAGAGGGGCAGCAAAGAGGGAATCT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52637410..52637577 26863196 MeRIP-seq:(Medium) rs1456242331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 70564 RMVar_ID_70564 Human_SNP_ID_669243674 m1A Human chr19 - 52648985 52648954 52648985 GCAGGGCATGAAAACTGTCGCTGGAGCTGGGCAAGAGGGTGGAGGCTGCTTTGGAAGCTGGGCCT GCAGGGCATGAAAACTGTCGCTGGAGCTGGGC_______________________________CT GGCCCAGCTTCCAAAGCAGCCTCCACCCTCTT G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52648937..52649174 26863196 MeRIP-seq:(Medium) rs1356853460 Functional Loss DEL dbSNP153 33..63 33 - - - Human_RBP_ID_9426411,Human_RBP_ID_24374722,Human_RBP_ID_27839637 RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 70565 RMVar_ID_70565 Human_SNP_ID_669248798 m1A Human chr19 - 52670137 52670110 52670138 GATTGGAATGAGGCAGGGTGGAGCAGGTGATCAGAATGAGTCAAGGTGGAGCAGGTGATTGGAAT GATTGGAATGAGGCAGGGTGGAGCAGGTGAT____________________________TGGAAT AATCACCTGCTCCACCTTGACTCATTCTG A ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52670087..52670301 26863196 MeRIP-seq:(Medium) rs1281884195 Functional Loss DEL dbSNP153 32..59 33 - - - RMVar_hsa_circ_313281,RMVar_hsa_circ_311724 70566 RMVar_ID_70566 Human_SNP_ID_669248808 m1A Human chr19 - 52670137 52670137 52670137 GATTGGAATGAGGCAGGGTGGAGCAGGTGATCAGAATGAGTCAAGGTGGAGCAGGTGATTGGAAT GATTGGAATGAGGCAGGGTGGAGCAGGTGATCGGAATGAGTCAAGGTGGAGCAGGTGATTGGAAT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52670087..52670301 26863196 MeRIP-seq:(Medium) rs1174977889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313281,RMVar_hsa_circ_311724 70567 RMVar_ID_70567 Human_SNP_ID_669248810 m1A Human chr19 - 52670140 52670140 52670140 GGTGATTGGAATGAGGCAGGGTGGAGCAGGTGATCAGAATGAGTCAAGGTGGAGCAGGTGATTGG GGTGATTGGAATGAGGCAGGGTGGAGCAGGTGTTCAGAATGAGTCAAGGTGGAGCAGGTGATTGG T A ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52670074..52670308 26863196 MeRIP-seq:(Medium) rs558012267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313281,RMVar_hsa_circ_311724 70568 RMVar_ID_70568 Human_SNP_ID_669254639 m1A Human chr19 - 52688548 52688547 52688549 TGAGGAGCAGAACCCCGGGGGAAAATAAAACAAGAGCTAGAGAGAGAAGGGGAGAATGAGAGATA TGAGGAGCAGAACCCCGGGGGAAAATAAAAC__GAGCTAGAGAGAGAAGGGGAGAATGAGAGATA CTT C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52688502..52688663 26863196 MeRIP-seq:(Medium) rs1298942889 Functional Loss DEL dbSNP153 32..33 33 - - - 70569 RMVar_ID_70569 Human_SNP_ID_669254951 m1A Human chr19 + 52689556 52689556 52689556 GATGAGCCTCCCTCTTTGCTGCCCCTCTCCCTACCTTGCTGTCCTTCATGTCTCTGTACATCCAG GATGAGCCTCCCTCTTTGCTGCCCCTCTCCCTGCCTTGCTGTCCTTCATGTCTCTGTACATCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52689539..52689757 26863196 MeRIP-seq:(Medium) rs994676663 Functional Loss SNV dbSNP153 33..33 33 - - - 70570 RMVar_ID_70570 Human_SNP_ID_669265515 m1A Human chr19 - 52723109 52723109 52723109 GGGAAAAAGAAAAGAAAACAAGAGCTAGAAAGAGAAGGGGAGAATGAGAGATATGCACAGAATTA GGGAAAAAGAAAAGAAAACAAGAGCTAGAAAGGGAAGGGGAGAATGAGAGATATGCACAGAATTA T C ZNF611 Ensembl:ENSG00000213020 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:52723078..52723168 26863196 MeRIP-seq:(Medium) rs1413733257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92646,RMVar_hsa_circ_196169 70571 RMVar_ID_70571 Human_SNP_ID_669265520 m1A Human chr19 - 52723122 52723120 52723122 GAGCACAATCCCAGGGAAAAAGAAAAGAAAACAAGAGCTAGAAAGAGAAGGGGAGAATGAGAGAT GAGCACAATCCCAGGGAAAAAGAAAAGAAAAC__GAGCTAGAAAGAGAAGGGGAGAATGAGAGAT CTT C ZNF611 Ensembl:ENSG00000213020 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52723000..52723282 26863196 MeRIP-seq:(Medium) rs901281259 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_92646,RMVar_hsa_circ_196169 70572 RMVar_ID_70572 Human_SNP_ID_669265521 m1A Human chr19 - 52723122 52723120 52723123 GAGCACAATCCCAGGGAAAAAGAAAAGAAAACAAGAGCTAGAAAGAGAAGGGGAGAATGAGAGAT GAGCACAATCCCAGGGAAAAAGAAAAGAAAA___GAGCTAGAAAGAGAAGGGGAGAATGAGAGAT CTTG C ZNF611 Ensembl:ENSG00000213020 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52723000..52723282 26863196 MeRIP-seq:(Medium) rs1486331570 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_92646,RMVar_hsa_circ_196169 70573 RMVar_ID_70573 Human_SNP_ID_669266044 m1A Human chr19 - 52724893 52724893 52724893 AAATAAGAAAGCAGGAGGAGAAAAGCAACTGGAGAAATGTAGAGAAGAGCTAGATGTACAGAGAT AAATAAGAAAGCAGGAGGAGAAAAGCAACTGGTGAAATGTAGAGAAGAGCTAGATGTACAGAGAT T A ZNF611 Ensembl:ENSG00000213020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52724560..52725022 26863196 MeRIP-seq:(Medium) rs1487521471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2569610,Human_RBP_ID_13504955 RMVar_hsa_circ_92646,RMVar_hsa_circ_196169 70574 RMVar_ID_70574 Human_SNP_ID_669269327 m1A Human chr19 + 52734966 52734966 52734966 GTCCCAGGGACAGAAGCCCTGGGAACCTAGTTAGCGCAGACTTAATACAACACAGAGCAAAACTC GTCCCAGGGACAGAAGCCCTGGGAACCTAGTTGGCGCAGACTTAATACAACACAGAGCAAAACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52734951..52735026 26863196 MeRIP-seq:(Medium) rs917990459 Functional Loss SNV dbSNP153 33..33 33 - - - 70575 RMVar_ID_70575 Human_SNP_ID_669284106 m1A Human chr19 - 52785571 52785571 52785571 GACATTGAGGAAGATTGAAAGATTGGGGAGAAAGAACAACAAGAGGTTAAATAAGGACCGGGCGC GACATTGAGGAAGATTGAAAGATTGGGGAGAAGGAACAACAAGAGGTTAAATAAGGACCGGGCGC T C ZNF600 Ensembl:ENSG00000189190 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52785568..52785745 26863196 MeRIP-seq:(Medium) rs560490606 Functional Loss SNV dbSNP153 33..33 33 - - - 70576 RMVar_ID_70576 Human_SNP_ID_669284192 m1A Human chr19 - 52785832 52785832 52785832 AAGATGAAGGACAGCAAGGTAGGGAGAGGGGCAGCAAAGAGGGAGGCTCACCAGAGTGAGGGAGA AAGATGAAGGACAGCAAGGTAGGGAGAGGGGCGGCAAAGAGGGAGGCTCACCAGAGTGAGGGAGA T C ZNF600 Ensembl:ENSG00000189190 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:52785824..52785912 26863196 MeRIP-seq:(Medium) rs922118756 Functional Loss SNV dbSNP153 33..33 33 - - - 70577 RMVar_ID_70577 Human_SNP_ID_669284199 m1A Human chr19 - 52785861 52785861 52785861 GAAATGTAGAGAAAAGCTAGATGTACAGAAAGATGAAGGACAGCAAGGTAGGGAGAGGGGCAGCA GAAATGTAGAGAAAAGCTAGATGTACAGAAAGCTGAAGGACAGCAAGGTAGGGAGAGGGGCAGCA T G ZNF600 Ensembl:ENSG00000189190 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:52785812..52786003 26863196 MeRIP-seq:(Medium) rs776436335 Functional Loss SNV dbSNP153 33..33 33 - - - 70578 RMVar_ID_70578 Human_SNP_ID_669371125 m1A Human chr19 + 53089787 53089787 53089789 TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTACATATCTCATCCTCACCTTCCCTCCCTGGCTC TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTGCGTATCTCATCCTCACCTTCCCTCCCTGGCTC ACA GCG NONHSAG026435.2 RNACentral:URS00008B32DF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53089738..53089910 26863196 MeRIP-seq:(Medium) rs386810637 Functional Loss MNV dbSNP153 33..35 33 - - - 70579 RMVar_ID_70579 Human_SNP_ID_669371126 m1A Human chr19 + 53089787 53089787 53089787 TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTACATATCTCATCCTCACCTTCCCTCCCTGGCTC TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTCCATATCTCATCCTCACCTTCCCTCCCTGGCTC A C NONHSAG026435.2 RNACentral:URS00008B32DF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53089738..53089910 26863196 MeRIP-seq:(Medium) rs7258975 Functional Loss SNV dbSNP153 33..33 33 - - - 70580 RMVar_ID_70580 Human_SNP_ID_669371127 m1A Human chr19 + 53089787 53089787 53089787 TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTACATATCTCATCCTCACCTTCCCTCCCTGGCTC TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTGCATATCTCATCCTCACCTTCCCTCCCTGGCTC A G NONHSAG026435.2 RNACentral:URS00008B32DF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53089738..53089910 26863196 MeRIP-seq:(Medium) rs7258975 Functional Loss SNV dbSNP153 33..33 33 - - - 70581 RMVar_ID_70581 Human_SNP_ID_669371128 m1A Human chr19 + 53089787 53089787 53089787 TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTACATATCTCATCCTCACCTTCCCTCCCTGGCTC TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTTCATATCTCATCCTCACCTTCCCTCCCTGGCTC A T NONHSAG026435.2 RNACentral:URS00008B32DF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53089738..53089910 26863196 MeRIP-seq:(Medium) rs7258975 Functional Loss SNV dbSNP153 33..33 33 - - - 70582 RMVar_ID_70582 Human_SNP_ID_669436446 m1A Human chr19 + 53333173 53333172 53333173 GAGGTGTTACTTTGTCGCCCAGGCTAACTTGGACCCCCCCCCCGGCTCAGCGATCCTCCTGCCAC GAGGTGTTACTTTGTCGCCCAGGCTAACTTGG_CCCCCCCCCCGGCTCAGCGATCCTCCTGCCAC GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:53333151..53333200 26863196 MeRIP-seq:(Medium) rs1364513597 Functional Loss DEL dbSNP153 33..33 33 - - - 70583 RMVar_ID_70583 Human_SNP_ID_669436447 m1A Human chr19 + 53333173 53333173 53333173 GAGGTGTTACTTTGTCGCCCAGGCTAACTTGGACCCCCCCCCCGGCTCAGCGATCCTCCTGCCAC GAGGTGTTACTTTGTCGCCCAGGCTAACTTGGCCCCCCCCCCCGGCTCAGCGATCCTCCTGCCAC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:53333151..53333200 26863196 MeRIP-seq:(Medium) rs954560818 Functional Loss SNV dbSNP153 33..33 33 - - - 70584 RMVar_ID_70584 Human_SNP_ID_669436679 m1A Human chr19 - 53333774 53333774 53333774 AGAGCAAAACTCACCGCTGCGGTGGGACCATCACTCCATGCGATCCGCTTCCGGGTTTGCGCGAA AGAGCAAAACTCACCGCTGCGGTGGGACCATCTCTCCATGCGATCCGCTTCCGGGTTTGCGCGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:53333762..53333839;chr19:53333766..53333852 26863196 MeRIP-seq:(Medium) rs1312717283 Functional Loss SNV dbSNP153 33..33 33 - - - 70585 RMVar_ID_70585 Human_SNP_ID_669438806 m1A Human chr19 - 53341254 53341254 53341254 CTTCCTCTTCCGGGTTTCTTCCTCACGTACCAAGAGTCTTTAGAAGTCAATCCTGAATGTTAAAA CTTCCTCTTCCGGGTTTCTTCCTCACGTACCAGGAGTCTTTAGAAGTCAATCCTGAATGTTAAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53341242..53341355 26863196 MeRIP-seq:(Medium) rs1198593897 Functional Loss SNV dbSNP153 33..33 33 - - - 70586 RMVar_ID_70586 Human_SNP_ID_669454638 m1A Human chr19 - 53396226 53396226 53396226 GTTATACCCTCATCCCCACTCTCTAGCACCCCAGATCCCCAGGTGTCCTCCCTGCTGTGCTTCTC GTTATACCCTCATCCCCACTCTCTAGCACCCCCGATCCCCAGGTGTCCTCCCTGCTGTGCTTCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:53396209..53396293 26863196 MeRIP-seq:(Medium) rs560386803 Functional Loss SNV dbSNP153 33..33 33 - - - 70587 RMVar_ID_70587 Human_SNP_ID_669464977 m1A Human chr19 + 53432011 53432011 53432011 CGTGCAGACCAGGAAGCGGATAGCGTGGAGTGACGGTGCCACCGCGGCGCGTGAGTTTCGCCCTG CGTGCAGACCAGGAAGCGGATAGCGTGGAGTGGCGGTGCCACCGCGGCGCGTGAGTTTCGCCCTG A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding exon,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53432002..53432082 26863196 MeRIP-seq:(Medium) rs1021612566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4545851,Human_RBP_ID_5586481 Human_Splice_Rec_2041109,Human_Splice_Rec_2041111,Human_Splice_Rec_2041121 RMVar_hsa_circ_311675 70588 RMVar_ID_70588 Human_SNP_ID_669465426 m1A Human chr19 + 53433100 53433100 53433100 AATTTAACGGGGAGAGCAAAGGAGGCGCAGAGATGGTGTTGCGGGAAACTGAGGACTAGACAGAC AATTTAACGGGGAGAGCAAAGGAGGCGCAGAGGTGGTGTTGCGGGAAACTGAGGACTAGACAGAC A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53433092..53433172 26863196 MeRIP-seq:(Medium) rs1319954429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8199680,Human_RBP_ID_18947450,Human_RBP_ID_21980231 RMVar_hsa_circ_311675 70589 RMVar_ID_70589 Human_SNP_ID_669467936 m1A Human chr19 - 53441805 53441805 53441805 CTCCGGTTCCTCCTTCCTCCACTCGGCATTGCAGACTCCTCTCTGTGATTATGAATTAAAAAAGA CTCCGGTTCCTCCTTCCTCCACTCGGCATTGCTGACTCCTCTCTGTGATTATGAATTAAAAAAGA T A AC022137.4 Ensembl:ENSG00000287608 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:53441792..53442021 26863196 MeRIP-seq:(Medium) rs1482323954 Functional Loss SNV dbSNP153 33..33 33 - - - 70590 RMVar_ID_70590 Human_SNP_ID_669468302 m1A Human chr19 + 53443410 53443410 53443410 TAAGAAGTCCAGTGGAGTCAAAGGAATGAGAAAAGACAAGTTAAGAATGCATAAGGTGGGTCCAG TAAGAAGTCCAGTGGAGTCAAAGGAATGAGAATAGACAAGTTAAGAATGCATAAGGTGGGTCCAG A T TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:53443375..53443493 26863196 MeRIP-seq:(Medium) rs1396977448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 70591 RMVar_ID_70591 Human_SNP_ID_669494790 m1A Human chr19 - 53538205 53538205 53538205 GGCCCCCATCGCCCCCAATGACGCTCGCGTGCACCCGTGTCACAGTTACGGGGACAGGGCCGCCG GGCCCCCATCGCCCCCAATGACGCTCGCGTGCCCCCGTGTCACAGTTACGGGGACAGGGCCGCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53538154..53538806 26863196 MeRIP-seq:(Medium) rs1178438492 Functional Loss SNV dbSNP153 33..33 33 - - - 70592 RMVar_ID_70592 Human_SNP_ID_669494799 m1A Human chr19 - 53538221 53538221 53538221 AACGCGCACCCAGCACGGCCCCCATCGCCCCCAATGACGCTCGCGTGCACCCGTGTCACAGTTAC AACGCGCACCCAGCACGGCCCCCATCGCCCCCTATGACGCTCGCGTGCACCCGTGTCACAGTTAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:53538172..53538791;chr19:53538170..53538384 26863196 MeRIP-seq:(Medium) rs1232391037 Functional Loss SNV dbSNP153 33..33 33 - - - 70593 RMVar_ID_70593 Human_SNP_ID_669529107 m1A Human chr19 + 53655093 53655093 53655093 GATAGCACGCTGGCCTTCACCTTCATTGTGCCATGGCAGCTTTCGTGTGAGCCACTGACTCGTGT GATAGCACGCTGGCCTTCACCTTCATTGTGCCGTGGCAGCTTTCGTGTGAGCCACTGACTCGTGT A G lnc-DPRX-2 RNACentral:URS0000D5C855 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:53654965..53655205 26863196 MeRIP-seq:(Medium) rs948995825 Functional Loss SNV dbSNP153 33..33 33 - - - 70594 RMVar_ID_70594 Human_SNP_ID_669599926 m1A Human chr19 - 53866419 53866419 53866419 GCCTGAGTCCCTCCCTCTGGCCGCGTTCACTCACCGCGCTCTGCAGTCGTCCCGGGCGCGGCCTG GCCTGAGTCCCTCCCTCTGGCCGCGTTCACTCTCCGCGCTCTGCAGTCGTCCCGGGCGCGGCCTG T A MYADM-AS1 Ensembl:ENSG00000228323 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53866402..53866473 26863196 MeRIP-seq:(Medium) rs1428569501 Functional Loss SNV dbSNP153 33..33 33 - - - 70595 RMVar_ID_70595 Human_SNP_ID_669600420 m1A Human chr19 - 53868226 53868188 53868226 TCCAGGCCCTCAGCCCCTCCTCCCTCGGACCCAGGAGTCCAGACCCCCCAGCCCCTCCTGCCTCG TCCAGGCCCTCAGCCCCTCCTCCCTCGGACCC_________________________________ CGGGTCCGAGGCAGGAGGGGCTGGGGGGTCTGGACTCCT C MYADM-AS1 Ensembl:ENSG00000228323 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53868218..53868368 26863196 MeRIP-seq:(Medium) rs1470566834 Functional Loss DEL dbSNP153 33..65 33 - - - 70596 RMVar_ID_70596 Human_SNP_ID_669600434 m1A Human chr19 - 53868226 53868226 53868226 TCCAGGCCCTCAGCCCCTCCTCCCTCGGACCCAGGAGTCCAGACCCCCCAGCCCCTCCTGCCTCG TCCAGGCCCTCAGCCCCTCCTCCCTCGGACCCCGGAGTCCAGACCCCCCAGCCCCTCCTGCCTCG T G MYADM-AS1 Ensembl:ENSG00000228323 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53868218..53868368 26863196 MeRIP-seq:(Medium) rs1327291316 Functional Loss SNV dbSNP153 33..33 33 - - - 70597 RMVar_ID_70597 Human_SNP_ID_669600978 m1A Human chr19 - 53869931 53869931 53869931 CCCAGCCCCTCCTCCCTCGGACCGAGGAGCCCAGGCCCCCAGCCCCTCCTCCCTCGGACCCCGGA CCCAGCCCCTCCTCCCTCGGACCGAGGAGCCCTGGCCCCCAGCCCCTCCTCCCTCGGACCCCGGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53869927..53870174 26863196 MeRIP-seq:(Medium) rs1366278550 Functional Loss SNV dbSNP153 33..33 33 - - - 70598 RMVar_ID_70598 Human_SNP_ID_669601045 m1A Human chr19 - 53870021 53870021 53870021 TCCAGACCCCCAGCCCCTCCTCCCTCGGACCCAGGAGCCCAGGCCCCCAGCCCCTCCTCCCTCGG TCCAGACCCCCAGCCCCTCCTCCCTCGGACCCCGGAGCCCAGGCCCCCAGCCCCTCCTCCCTCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53870016..53870144 26863196 MeRIP-seq:(Medium) rs1471316464 Functional Loss SNV dbSNP153 33..33 33 - - - 70599 RMVar_ID_70599 Human_SNP_ID_669602044 m1A Human chr19 + 53873551 53873551 53873551 TTTTTGCAGCCATGCCAGTGACGGTAACCCGCACCACCATCACAACCACCACGACGTCATCTTCG TTTTTGCAGCCATGCCAGTGACGGTAACCCGCGCCACCATCACAACCACCACGACGTCATCTTCG A G MYADM Ensembl:ENSG00000179820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53873526..53873597 26863196 MeRIP-seq:(Medium) rs781704036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912741,Human_RBP_ID_4558726,Human_RBP_ID_17387043,Human_RBP_ID_20417304,Human_RBP_ID_26816295 Human_Splice_Rec_2041532,Human_Splice_Rec_2041536,Human_Splice_Rec_2041540,Human_Splice_Rec_2041544,Human_Splice_Rec_2041546,Human_Splice_Rec_2041550,Human_Splice_Rec_2041554,Human_Splice_Rec_2041558,Human_Splice_Rec_2041560 RMVar_hsa_circ_104567,RMVar_hsa_circ_196212 70600 RMVar_ID_70600 Human_SNP_ID_669612455 m1A Human chr19 - 53906893 53906893 53906893 GTTGGGGACACCTAGTGGCGGCGGGTGAGATTACATGACGGGCACAGGCACTGGGCTGGTGGGGC GTTGGGGACACCTAGTGGCGGCGGGTGAGATTGCATGACGGGCACAGGCACTGGGCTGGTGGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53906848..53906961 26863196 MeRIP-seq:(Medium) rs1158020271 Functional Loss SNV dbSNP153 33..33 33 - - - 70601 RMVar_ID_70601 Human_SNP_ID_669630325 m1A Human chr19 + 53963020 53963020 53963020 GCCGCAGCCTCCTCCTCGCCGCCCCCCTCCCCAGCCCCGCCGGCCCCGGGCCCCCCGCTTCTGCC GCCGCAGCCTCCTCCTCGCCGCCCCCCTCCCCCGCCCCGCCGGCCCCGGGCCCCCCGCTTCTGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53962971..53979897 26863196 MeRIP-seq:(Medium) rs1236046749 Functional Loss SNV dbSNP153 33..33 33 - - - 70602 RMVar_ID_70602 Human_SNP_ID_669636349 m1A Human chr19 - 53983767 53983767 53983767 GGGGCCTTTGCACGTGCTGCTCTGCCTGCCACACTCCTGCCCCAGCTCCGCCCTGCTGGCTTCTT GGGGCCTTTGCACGTGCTGCTCTGCCTGCCACTCTCCTGCCCCAGCTCCGCCCTGCTGGCTTCTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53983717..53984018 26863196 MeRIP-seq:(Medium) rs970658960 Functional Loss SNV dbSNP153 33..33 33 - - - 70603 RMVar_ID_70603 Human_SNP_ID_669636768 m1A Human chr19 + 53985394 53985394 53985394 TTCTCTCCGAGGCCTGTGTGGAAGGACCAGGAAGAGAGAGACTGAAGGTCCCTAGGAAGAATTCT TTCTCTCCGAGGCCTGTGTGGAAGGACCAGGAGGAGAGAGACTGAAGGTCCCTAGGAAGAATTCT A G CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:53985380..53985473 26863196 MeRIP-seq:(Medium) rs903392965 Functional Loss SNV dbSNP153 33..33 33 - - - 70604 RMVar_ID_70604 Human_SNP_ID_669636919 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAAC____________GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA C CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 22..33 33 - - - 70605 RMVar_ID_70605 Human_SNP_ID_669636920 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAACGA__________GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA CGA CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 24..33 33 - - - 70606 RMVar_ID_70606 Human_SNP_ID_669636921 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAACGAGA________GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA CGAGA CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 26..33 33 - - - 70607 RMVar_ID_70607 Human_SNP_ID_669636922 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAACGAGAGA______GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA CGAGAGA CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 28..33 33 - - - 70608 RMVar_ID_70608 Human_SNP_ID_669636923 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAACGAGAGAGA____GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA CGAGAGAGA CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 30..33 33 - - - 70609 RMVar_ID_70609 Human_SNP_ID_669636924 m1A Human chr19 + 53985949 53985937 53985949 AGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG AGTCTGAAGGCCAAACAGAACGAGAGAGAGA__GAGAGAGAGAGAAAGAATGAGGTTGAGGGTAG CGAGAGAGAGAGA CGAGAGAGAGA CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53985899..53986267 26863196 MeRIP-seq:(Medium) rs35381014 Functional Loss DEL dbSNP153 32..33 33 - - - 70610 RMVar_ID_70610 Human_SNP_ID_669636936 m1A Human chr19 + 53985939 53985938 53985939 TGGATTCTAGAGTCTGAAGGCCAAACAGAACGAGAGAGAGAGAGAGAGAGAGAGAAAGAATGAGG TGGATTCTAGAGTCTGAAGGCCAAACAGAACG_GAGAGAGAGAGAGAGAGAGAGAAAGAATGAGG GA G CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:53985894..53986093 26863196 MeRIP-seq:(Medium) rs1246394572 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_140272,Human_RBP_ID_17068445 70611 RMVar_ID_70611 Human_SNP_ID_669644564 m1A Human chr19 - 54012058 54012058 54012058 GCCGGCCCCCACGCCGCAGCCCAGGGACCAGGAGTACTCGTAGGTGAGGCGTGGGGCCGGGGGAG GCCGGCCCCCACGCCGCAGCCCAGGGACCAGGGGTACTCGTAGGTGAGGCGTGGGGCCGGGGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:53999709..54012279 32194978 MeRIP-seq:(Medium) rs913639979 Functional Loss SNV dbSNP153 33..33 33 - - - 70612 RMVar_ID_70612 Human_SNP_ID_669668985 m1A Human chr19 - 54096433 54096430 54096440 AGGCAGGCAGAGAGAGAGGCAGGCAGAGAGAGAGGGAGGCAGAGAGAGAGGGAGGCAGAGAGAGA AGGCAGGCAGAGAGAGAGGCAGGCAAAGAGAGAGGCAGGCAGAGAGAGAGGGAGGCAGAGAGAGA CCCTCTCTCTC GCCTCTCTCTT OSCAR Ensembl:ENSG00000170909 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54096430..54096502 26863196 MeRIP-seq:(Medium) rs1444295078 Functional Loss MNV dbSNP153 26..36 33 - - - 70613 RMVar_ID_70613 Human_SNP_ID_669668986 m1A Human chr19 - 54096433 54096431 54096433 AGGCAGGCAGAGAGAGAGGCAGGCAGAGAGAGAGGGAGGCAGAGAGAGAGGGAGGCAGAGAGAGA AGGCAGGCAGAGAGAGAGGCAGGCAGAGAGAG__GGAGGCAGAGAGAGAGGGAGGCAGAGAGAGA CCT C OSCAR Ensembl:ENSG00000170909 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54096430..54096502 26863196 MeRIP-seq:(Medium) rs60414829 Functional Loss DEL dbSNP153 33..34 33 - - - 70614 RMVar_ID_70614 Human_SNP_ID_669671216 m1A Human chr19 - 54103117 54103117 54103117 CCTTGTCCCAGGCATTCTTGAGGAAGGCGCCGACTCCTGAAGGGGTGGCAAGAAGCGTCACCCCT CCTTGTCCCAGGCATTCTTGAGGAAGGCGCCGTCTCCTGAAGGGGTGGCAAGAAGCGTCACCCCT T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54103101..54103225 26863410 MeRIP-seq:(Medium) rs1244258293 Functional Loss SNV dbSNP153 33..33 33 - - - 70615 RMVar_ID_70615 Human_SNP_ID_669671217 m1A Human chr19 - 54103117 54103117 54103117 CCTTGTCCCAGGCATTCTTGAGGAAGGCGCCGACTCCTGAAGGGGTGGCAAGAAGCGTCACCCCT CCTTGTCCCAGGCATTCTTGAGGAAGGCGCCGGCTCCTGAAGGGGTGGCAAGAAGCGTCACCCCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54103101..54103225 26863410 MeRIP-seq:(Medium) rs1244258293 Functional Loss SNV dbSNP153 33..33 33 - - - 70616 RMVar_ID_70616 Human_SNP_ID_669672238 m1A Human chr19 + 54106010 54106002 54106011 ATGATCAACAAGGCCACGCCCTACAACTACCCAGGTGAGTGGGGGCCAGGCAGGGATCCCCGGAA ATGATCAACAAGGCCACGCCCTACA_________GTGAGTGGGGGCCAGGCAGGGATCCCCGGAA AACTACCCAG A NDUFA3 Ensembl:ENSG00000170906 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:54105976..54106025 32194978 MeRIP-seq:(Medium) rs778135220 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_772037,Human_RBP_ID_914268,Human_RBP_ID_1018012,Human_RBP_ID_17271964,Human_RBP_ID_17656354,Human_RBP_ID_23114827,Human_RBP_ID_26816303 Human_Splice_Rec_2041860,Human_Splice_Rec_2041861,Human_Splice_Rec_2041868,Human_Splice_Rec_2041869,Human_Splice_Rec_2041876,Human_Splice_Rec_2041877,Human_Splice_Rec_2041884,Human_Splice_Rec_2041890,Human_Splice_Rec_2041891,Human_Splice_Rec_2041896,Human_Splice_Rec_2041897,Human_Splice_Rec_2041902,Human_Splice_Rec_2041903,Human_Splice_Rec_2041908,Human_Splice_Rec_2041909,Human_Splice_Rec_2041912,Human_Splice_Rec_2041913,Human_Splice_Rec_2041918,Human_Splice_Rec_2041919,Human_Splice_Rec_2041922,Human_Splice_Rec_2041923,Human_Splice_Rec_2041929 RMVar_hsa_circ_120853,RMVar_hsa_circ_196219 70617 RMVar_ID_70617 Human_SNP_ID_669672242 m1A Human chr19 + 54106010 54106010 54106010 ATGATCAACAAGGCCACGCCCTACAACTACCCAGGTGAGTGGGGGCCAGGCAGGGATCCCCGGAA ATGATCAACAAGGCCACGCCCTACAACTACCCGGGTGAGTGGGGGCCAGGCAGGGATCCCCGGAA A G NDUFA3 Ensembl:ENSG00000170906 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:54105976..54106025 32194978 MeRIP-seq:(Medium) rs368243962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772037,Human_RBP_ID_914268,Human_RBP_ID_1018012,Human_RBP_ID_17271964,Human_RBP_ID_17656354,Human_RBP_ID_23114827,Human_RBP_ID_26816303 Human_Splice_Rec_2041860,Human_Splice_Rec_2041861,Human_Splice_Rec_2041868,Human_Splice_Rec_2041869,Human_Splice_Rec_2041876,Human_Splice_Rec_2041877,Human_Splice_Rec_2041884,Human_Splice_Rec_2041890,Human_Splice_Rec_2041891,Human_Splice_Rec_2041896,Human_Splice_Rec_2041897,Human_Splice_Rec_2041902,Human_Splice_Rec_2041903,Human_Splice_Rec_2041908,Human_Splice_Rec_2041909,Human_Splice_Rec_2041912,Human_Splice_Rec_2041913,Human_Splice_Rec_2041918,Human_Splice_Rec_2041919,Human_Splice_Rec_2041922,Human_Splice_Rec_2041923,Human_Splice_Rec_2041929 RMVar_hsa_circ_120853,RMVar_hsa_circ_196219 70618 RMVar_ID_70618 Human_SNP_ID_669672950 m1A Human chr19 + 54108056 54108056 54108056 ACCTGCACCGGGGCCAGCTCTGGAGTCAGCGCATTTCCTGCTCGGCGTCCATCCCGTGGCACTCG ACCTGCACCGGGGCCAGCTCTGGAGTCAGCGCCTTTCCTGCTCGGCGTCCATCCCGTGGCACTCG A C NDUFA3 Ensembl:ENSG00000170906 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54106994..54108067 26863196 MeRIP-seq:(Medium) rs1300696950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17083395,Human_RBP_ID_20417753 70619 RMVar_ID_70619 Human_SNP_ID_669673024 m1A Human chr19 - 54108180 54108178 54108180 CCCAGGCAATGCGGAGAATGAGCCTCCAGAGAAAGAGACACTGTCCCCGCCCAGAAGGACTCCTG CCCAGGCAATGCGGAGAATGAGCCTCCAGAGA__GAGACACTGTCCCCGCCCAGAAGGACTCCTG CTT C TFPT Ensembl:ENSG00000105619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54107988..54108422 26863196 MeRIP-seq:(Medium) rs1353291754 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_2041946,Human_Splice_Rec_2041956,Human_Splice_Rec_2041964,Human_Splice_Rec_2041974 70620 RMVar_ID_70620 Human_SNP_ID_669673025 m1A Human chr19 - 54108180 54108180 54108180 CCCAGGCAATGCGGAGAATGAGCCTCCAGAGAAAGAGACACTGTCCCCGCCCAGAAGGACTCCTG CCCAGGCAATGCGGAGAATGAGCCTCCAGAGAGAGAGACACTGTCCCCGCCCAGAAGGACTCCTG T C TFPT Ensembl:ENSG00000105619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54107988..54108422 26863196 MeRIP-seq:(Medium) rs766850986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2041946,Human_Splice_Rec_2041956,Human_Splice_Rec_2041964,Human_Splice_Rec_2041974 70621 RMVar_ID_70621 Human_SNP_ID_669673594 m1A Human chr19 + 54109839 54109794 54109839 CCCTCCCTCAGTCCCAGTGCTCAGCCCTCTCCACCCGGCCCTCCCTCAGTCCCAGTGCTCAGCCC _________________________________CCCGGCCCTCCCTCAGTCCCAGTGCTCAGCCC GCCCTCCACCCGGCCCTCCCTCAGTCCCAGTGCTCAGCCCTCTCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr19:54109774..54109916;chr19:54109742..54110161;chr19:54109741..54109953 26863196 MeRIP-seq:(Medium) rs1568567540 Functional Loss DEL dbSNP153 1..33 33 - - - 70622 RMVar_ID_70622 Human_SNP_ID_669673598 m1A Human chr19 - 54109834 54109796 54109834 GAGCACTGGGACTGAGGGAGGGCCGGGTGGAGAGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG GAGCACTGGGACTGAGGGAGGGCCGGGTGGAG_________________________________ CCTCCACCCGGCCCTCCCTCAGTCCCAGTGCTCAGCCCT C TFPT Ensembl:ENSG00000105619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54108073..54115650;chr19:54109752..54110177 26863196 MeRIP-seq:(Medium) rs1244545412 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_263356,Human_RBP_ID_3581601,Human_RBP_ID_5320568,Human_RBP_ID_8100794,Human_RBP_ID_8196849,Human_RBP_ID_8233214,Human_RBP_ID_8942238,Human_RBP_ID_9425442,Human_RBP_ID_22524426,Human_RBP_ID_22718399,Human_RBP_ID_26786016 70623 RMVar_ID_70623 Human_SNP_ID_669673637 m1A Human chr19 - 54109834 54109832 54109834 GAGCACTGGGACTGAGGGAGGGCCGGGTGGAGAGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG GAGCACTGGGACTGAGGGAGGGCCGGGTGGAG__GGCTGAGCACTGGGACTGAGGGAGGGCCGGG CCT C TFPT Ensembl:ENSG00000105619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54108073..54115650;chr19:54109752..54110177 26863196 MeRIP-seq:(Medium) rs1158832713 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_263356,Human_RBP_ID_3581601,Human_RBP_ID_5320568,Human_RBP_ID_8100794,Human_RBP_ID_8196849,Human_RBP_ID_8233214,Human_RBP_ID_8942238,Human_RBP_ID_9425442,Human_RBP_ID_22524426,Human_RBP_ID_22718399,Human_RBP_ID_26786016 70624 RMVar_ID_70624 Human_SNP_ID_669673638 m1A Human chr19 - 54109834 54109834 54109834 GAGCACTGGGACTGAGGGAGGGCCGGGTGGAGAGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG GAGCACTGGGACTGAGGGAGGGCCGGGTGGAGGGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG T C TFPT Ensembl:ENSG00000105619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54108073..54115650;chr19:54109752..54110177 26863196 MeRIP-seq:(Medium) rs867627058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263356,Human_RBP_ID_3581601,Human_RBP_ID_5320568,Human_RBP_ID_8100794,Human_RBP_ID_8196849,Human_RBP_ID_8233214,Human_RBP_ID_8942238,Human_RBP_ID_9425442,Human_RBP_ID_22524426,Human_RBP_ID_22718399,Human_RBP_ID_26786016 70625 RMVar_ID_70625 Human_SNP_ID_669673639 m1A Human chr19 - 54109834 54109834 54109835 GAGCACTGGGACTGAGGGAGGGCCGGGTGGAGAGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG GAGCACTGGGACTGAGGGAGGGCCGGGTGGAAGGGGCTGAGCACTGGGACTGAGGGAGGGCCGGG TC CT TFPT Ensembl:ENSG00000105619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54108073..54115650;chr19:54109752..54110177 26863196 MeRIP-seq:(Medium) rs1555788232 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_263356,Human_RBP_ID_3581601,Human_RBP_ID_5320568,Human_RBP_ID_8100794,Human_RBP_ID_8196849,Human_RBP_ID_8233214,Human_RBP_ID_8942238,Human_RBP_ID_9425442,Human_RBP_ID_22524426,Human_RBP_ID_22718399,Human_RBP_ID_26786016 70626 RMVar_ID_70626 Human_SNP_ID_669675145 m1A Human chr19 - 54114526 54114526 54114526 GGGCTCCGGGAGCGAGATGAAGAGGAAGAGGCAGCCCGGGGTCGGCGGCGGCGCCAGCGGGAATT GGGCTCCGGGAGCGAGATGAAGAGGAAGAGGCGGCCCGGGGTCGGCGGCGGCGCCAGCGGGAATT T C TFPT Ensembl:ENSG00000105619 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:54114477..54114725;chr19:54114406..54114732 26863196 MeRIP-seq:(Medium) rs1418839467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5117103 Human_Splice_Rec_2041941,Human_Splice_Rec_2041951,Human_Splice_Rec_2041961,Human_Splice_Rec_2041969 70627 RMVar_ID_70627 Human_SNP_ID_669675161 m1A Human chr19 + 54114554 54114554 54114554 GGGCTGCCTCTTCCTCTTCATCTCGCTCCCGGAGCCCTGAGCCGCCCAGACCACCTGACACAAAC GGGCTGCCTCTTCCTCTTCATCTCGCTCCCGGGGCCCTGAGCCGCCCAGACCACCTGACACAAAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54114394..54114734 26863196 MeRIP-seq:(Medium) rs1185242712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13506018 70628 RMVar_ID_70628 Human_SNP_ID_669675489 m1A Human chr19 + 54115597 54115597 54115597 TTCTCTGCTTAGCAGGATCGGTCCACAGCGGGACGTGAGTCCCTTTCCTCCTCGCGGCTTACCGC TTCTCTGCTTAGCAGGATCGGTCCACAGCGGGGCGTGAGTCCCTTTCCTCCTCGCGGCTTACCGC A G PRPF31 Ensembl:ENSG00000105618 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54115216..54115650 26863196 MeRIP-seq:(Medium) rs1205196358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97840,RMVar_hsa_circ_196220 70629 RMVar_ID_70629 Human_SNP_ID_669675490 m1A Human chr19 + 54115597 54115597 54115597 TTCTCTGCTTAGCAGGATCGGTCCACAGCGGGACGTGAGTCCCTTTCCTCCTCGCGGCTTACCGC TTCTCTGCTTAGCAGGATCGGTCCACAGCGGGTCGTGAGTCCCTTTCCTCCTCGCGGCTTACCGC A T PRPF31 Ensembl:ENSG00000105618 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54115216..54115650 26863196 MeRIP-seq:(Medium) rs1205196358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97840,RMVar_hsa_circ_196220 70630 RMVar_ID_70630 Human_SNP_ID_669675563 m1A Human chr19 + 54115796 54115796 54115796 TAACGCTAGAAACAGTGGTGCGCGGAGAGGAGAGGTGAGTGTGATGGGGACCACGGGGAGCGGGA TAACGCTAGAAACAGTGGTGCGCGGAGAGGAGTGGTGAGTGTGATGGGGACCACGGGGAGCGGGA A T PRPF31 Ensembl:ENSG00000105618 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:54115751..54115800 26863196 MeRIP-seq:(Medium) rs1415722671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239823 Human_Splice_Rec_2041977,Human_Splice_Rec_2042001,Human_Splice_Rec_2042015,Human_Splice_Rec_2042041 RMVar_hsa_circ_97840,RMVar_hsa_circ_196220 70631 RMVar_ID_70631 Human_SNP_ID_669676269 m1A Human chr19 - 54118242 54118242 54118242 AGGCCTGGGGAGGGACAGCAGCGTTCCCTAAAAACTTGCCCCGACAAAGTCCCTCCTTATTACTG AGGCCTGGGGAGGGACAGCAGCGTTCCCTAAACACTTGCCCCGACAAAGTCCCTCCTTATTACTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:54118239..54118400 26863196 MeRIP-seq:(Medium) rs587744285 Functional Loss SNV dbSNP153 33..33 33 - - - 70632 RMVar_ID_70632 Human_SNP_ID_669676275 m1A Human chr19 - 54118255 54118255 54118255 CAGAGACATCCCGAGGCCTGGGGAGGGACAGCAGCGTTCCCTAAAAACTTGCCCCGACAAAGTCC CAGAGACATCCCGAGGCCTGGGGAGGGACAGCGGCGTTCCCTAAAAACTTGCCCCGACAAAGTCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:54118251..54118400 26863196 MeRIP-seq:(Medium) rs771252001 Functional Loss SNV dbSNP153 33..33 33 - - - 70633 RMVar_ID_70633 Human_SNP_ID_669676286 m1A Human chr19 + 54118279 54118279 54118279 GGGAACGCTGCTGTCCCTCCCCAGGCCTCGGGATGTCTCTGGCAGATGAGCTCTTAGCTGATCTC GGGAACGCTGCTGTCCCTCCCCAGGCCTCGGGTTGTCTCTGGCAGATGAGCTCTTAGCTGATCTC A T PRPF31 Ensembl:ENSG00000105618 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:54115751..54118650 26863196 MeRIP-seq:(Medium) rs1555791188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239824,Human_RBP_ID_526574,Human_RBP_ID_22977523,Human_RBP_ID_26336742 Human_Splice_Rec_2041978,Human_Splice_Rec_2042002,Human_Splice_Rec_2042016,Human_Splice_Rec_2042042 Clinvar_Rec_292 RMVar_hsa_circ_97840,RMVar_hsa_circ_196220 70634 RMVar_ID_70634 Human_SNP_ID_669676303 m1A Human chr19 + 54118368 54118368 54118368 GGAGGAAGCTATGGGGAGGAAGAAGAGGAGCCAGCGATCGAGGATGTGCAGGAGGAGACACAGCT GGAGGAAGCTATGGGGAGGAAGAAGAGGAGCCGGCGATCGAGGATGTGCAGGAGGAGACACAGCT A G PRPF31 Ensembl:ENSG00000105618 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54118251..54118450 26863410 MeRIP-seq:(Medium) rs1399742310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239825,Human_RBP_ID_6783150,Human_RBP_ID_9346806,Human_RBP_ID_9381367,Human_RBP_ID_18998690,Human_RBP_ID_21980108,Human_RBP_ID_22070530,Human_RBP_ID_22449650,Human_RBP_ID_22977523,Human_RBP_ID_26336743,Human_RBP_ID_27815645 Human_Splice_Rec_2041978,Human_Splice_Rec_2041979,Human_Splice_Rec_2042003,Human_Splice_Rec_2042016,Human_Splice_Rec_2042017,Human_Splice_Rec_2042043,Human_Splice_Rec_2042055,Human_Splice_Rec_2042067,Human_Splice_Rec_2042091,Human_Splice_Rec_2042093 RMVar_hsa_circ_97840,RMVar_hsa_circ_196220 70635 RMVar_ID_70635 Human_SNP_ID_669677634 m1A Human chr19 + 54122822 54122822 54122822 CTCCCGAGAGGGCTTCCCCGCTGGCCTGACCCACGCTGCTCCCGCTGTGGTTGGAGCCGGTGGCA CTCCCGAGAGGGCTTCCCCGCTGGCCTGACCCCCGCTGCTCCCGCTGTGGTTGGAGCCGGTGGCA A C PRPF31 Ensembl:ENSG00000105618 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54122818..54122918 32194978 MeRIP-seq:(Medium) rs587593597 Functional Loss SNV dbSNP153 33..33 33 - - - 70636 RMVar_ID_70636 Human_SNP_ID_669677643 m1A Human chr19 + 54122872 54122859 54122873 TTGGAGCCGGTGGCATTGGAGTTGACATCCGAAGGTTGACACAGGGCAGGCACACGGAGATTTGG TTGGAGCCGGTGGCATTGGA______________GTTGACACAGGGCAGGCACACGGAGATTTGG AGTTGACATCCGAAG A PRPF31 Ensembl:ENSG00000105618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54122868..54123265 26863196 MeRIP-seq:(Medium) rs1432273287 Functional Loss DEL dbSNP153 21..34 33 - - - 70637 RMVar_ID_70637 Human_SNP_ID_669677647 m1A Human chr19 + 54122871 54122871 54122871 GTTGGAGCCGGTGGCATTGGAGTTGACATCCGAAGGTTGACACAGGGCAGGCACACGGAGATTTG GTTGGAGCCGGTGGCATTGGAGTTGACATCCGCAGGTTGACACAGGGCAGGCACACGGAGATTTG A C PRPF31 Ensembl:ENSG00000105618 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54122868..54123166 26863196 MeRIP-seq:(Medium) rs1054556825 Functional Loss SNV dbSNP153 33..33 33 - - - 70638 RMVar_ID_70638 Human_SNP_ID_669677994 m1A Human chr19 + 54123855 54123855 54123855 AGCACCGCATCTACGAGTATGTGGAGTCCCGGATGTCCTTCATCGCACCCAACCTGTCCATCATT AGCACCGCATCTACGAGTATGTGGAGTCCCGGGTGTCCTTCATCGCACCCAACCTGTCCATCATT A G PRPF31 Ensembl:ENSG00000105618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54123706..54123859 26863196 MeRIP-seq:(Medium) rs1555792899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1570738,Human_RBP_ID_3576149,Human_RBP_ID_8493372,Human_RBP_ID_13506067,Human_RBP_ID_18738880 Human_Splice_Rec_2041989,Human_Splice_Rec_2042013,Human_Splice_Rec_2042027,Human_Splice_Rec_2042053,Human_Splice_Rec_2042065,Human_Splice_Rec_2042077,Human_Splice_Rec_2042103,Human_Splice_Rec_2042121 70639 RMVar_ID_70639 Human_SNP_ID_669678176 m1A Human chr19 - 54124460 54124460 54124460 TGGGAGGGAGGGAGGAAGGGGGGGCGGTCAGAAGAAAGCAGAGAGGTGGGGGTGAGTAAATCTGC TGGGAGGGAGGGAGGAAGGGGGGGCGGTCAGAGGAAAGCAGAGAGGTGGGGGTGAGTAAATCTGC T C AC245052.4 Ensembl:ENSG00000237017 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54124458..54124593 26863196 MeRIP-seq:(Medium) rs1213821213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588780 70640 RMVar_ID_70640 Human_SNP_ID_669678267 m1A Human chr19 + 54124643 54124643 54124643 CACCGGCTACATCTACCACAGTGACATCGTGCAGTCCCTGCCACCGGTGAGCCCACTGCGTCATG CACCGGCTACATCTACCACAGTGACATCGTGCGGTCCCTGCCACCGGTGAGCCCACTGCGTCATG A G PRPF31 Ensembl:ENSG00000105618 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:54124476..54124675;chr19:54123454..54128213 32194978 MeRIP-seq:(Medium) rs776838460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18998691 Human_Splice_Rec_2041991,Human_Splice_Rec_2042029,Human_Splice_Rec_2042079,Human_Splice_Rec_2042105,Human_Splice_Rec_2042123 70641 RMVar_ID_70641 Human_SNP_ID_669679383 m1A Human chr19 + 54128083 54128083 54128083 ACCTCCCCCTCGCCCTCCCCAGGTGGGCTACGAACTGAAGGATGAGATCGAGCGCAAATTCGACA ACCTCCCCCTCGCCCTCCCCAGGTGGGCTACGTACTGAAGGATGAGATCGAGCGCAAATTCGACA A T PRPF31 Ensembl:ENSG00000105618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54128076..54128100 26863196 MeRIP-seq:(Medium) rs1218417233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22975800 Human_Splice_Rec_2041994,Human_Splice_Rec_2042032,Human_Splice_Rec_2042108,Human_Splice_Rec_2042126 70642 RMVar_ID_70642 Human_SNP_ID_669679420 m1A Human chr19 + 54128182 54128182 54128182 GCCGCTGCCTGCGCCCCTGGATGGACAGCGGAAGAAGCGAGGCGGCCGCAGGTGAGGGGCCCTGG GCCGCTGCCTGCGCCCCTGGATGGACAGCGGAGGAAGCGAGGCGGCCGCAGGTGAGGGGCCCTGG A G PRPF31 Ensembl:ENSG00000105618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54128043..54128209 26863196 MeRIP-seq:(Medium) rs1568597642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381371,Human_RBP_ID_18998693,Human_RBP_ID_26336750 Human_Splice_Rec_2041995,Human_Splice_Rec_2042033,Human_Splice_Rec_2042082,Human_Splice_Rec_2042083 70643 RMVar_ID_70643 Human_SNP_ID_669679537 m1A Human chr19 - 54128362 54128362 54128362 CGCTCTGGGAGTCTGACCTCTCCGAAGCTCATACGGTTGGCCTGCTTCCGGATCTCCGTCAGCCC CGCTCTGGGAGTCTGACCTCTCCGAAGCTCATTCGGTTGGCCTGCTTCCGGATCTCCGTCAGCCC T A lnc-TFPT-3 RNACentral:URS0000D58E6A lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54128311..54131323 32194978 MeRIP-seq:(Medium) rs780389815 Functional Loss SNV dbSNP153 33..33 33 - - - 70644 RMVar_ID_70644 Human_SNP_ID_669679811 m1A Human chr19 - 54128993 54128993 54128993 GCGACCAGGCCCTGCCCTCCAGCCACCGAGGCACCCCCTCCACCAGCCCGAAGCCCAGCGGTCAC GCGACCAGGCCCTGCCCTCCAGCCACCGAGGCCCCCCCTCCACCAGCCCGAAGCCCAGCGGTCAC T G lnc-TFPT-3 RNACentral:URS0000D58E6A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54128988..54129073 26863196 MeRIP-seq:(Medium) rs1437553036 Functional Loss SNV dbSNP153 33..33 33 - - - 70645 RMVar_ID_70645 Human_SNP_ID_669681739 m1A Human chr19 - 54133828 54133827 54133828 GAGAGAGAGGGGAGGTGGAGAGAGGGAGGGAGAGAGAGAGGGGAGGTGGAGAGGGAGGAAGAGAG GAGAGAGAGGGGAGGTGGAGAGAGGGAGGGAG_GAGAGAGGGGAGGTGGAGAGGGAGGAAGAGAG CT C lnc-TFPT-3 RNACentral:URS0000D58E6A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54133715..54133887 26863196 MeRIP-seq:(Medium) rs1302268948 Functional Loss DEL dbSNP153 33..33 33 - - - 70646 RMVar_ID_70646 Human_SNP_ID_669681742 m1A Human chr19 - 54133828 54133828 54133828 GAGAGAGAGGGGAGGTGGAGAGAGGGAGGGAGAGAGAGAGGGGAGGTGGAGAGGGAGGAAGAGAG GAGAGAGAGGGGAGGTGGAGAGAGGGAGGGAGGGAGAGAGGGGAGGTGGAGAGGGAGGAAGAGAG T C lnc-TFPT-3 RNACentral:URS0000D58E6A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54133715..54133887 26863196 MeRIP-seq:(Medium) rs149666820 Functional Loss SNV dbSNP153 33..33 33 - - - 70647 RMVar_ID_70647 Human_SNP_ID_669683432 m1A Human chr19 + 54137805 54137805 54137805 GGCCCGGTCAGCTTCCGCGGAGCCATCGGCAGACGCCGCGGCCTCCCTTGAGCCCCGACCCCCGT GGCCCGGTCAGCTTCCGCGGAGCCATCGGCAGGCGCCGCGGCCTCCCTTGAGCCCCGACCCCCGT A G CNOT3 Ensembl:ENSG00000088038 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:54137762..54138033;chr19:54137760..54137939 26863196 MeRIP-seq:(Medium) rs1399563403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241143,Human_RBP_ID_1570752,Human_RBP_ID_4546203,Human_RBP_ID_18420986,Human_RBP_ID_18738898 70648 RMVar_ID_70648 Human_SNP_ID_669683444 m1A Human chr19 + 54137823 54137823 54137823 GGAGCCATCGGCAGACGCCGCGGCCTCCCTTGAGCCCCGACCCCCGTCGTCAGAACAACCCCGGG GGAGCCATCGGCAGACGCCGCGGCCTCCCTTGGGCCCCGACCCCCGTCGTCAGAACAACCCCGGG A G CNOT3 Ensembl:ENSG00000088038 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54137775..54137928 26863196 MeRIP-seq:(Medium) rs1051556752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4546203,Human_RBP_ID_18192484,Human_RBP_ID_18420986,Human_RBP_ID_18738898 70649 RMVar_ID_70649 Human_SNP_ID_669683450 m1A Human chr19 + 54137847 54137847 54137847 CTCCCTTGAGCCCCGACCCCCGTCGTCAGAACAACCCCGGGCCCACTCCCCCAACCCCACTTCCG CTCCCTTGAGCCCCGACCCCCGTCGTCAGAACGACCCCGGGCCCACTCCCCCAACCCCACTTCCG A G CNOT3 Ensembl:ENSG00000088038 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:54137751..54137936 26863410 MeRIP-seq:(Medium) rs1338384090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4546204,Human_RBP_ID_5421815,Human_RBP_ID_5443424,Human_RBP_ID_5500096,Human_RBP_ID_18192484,Human_RBP_ID_18420986,Human_RBP_ID_23806666 70650 RMVar_ID_70650 Human_SNP_ID_669685310 m1A Human chr19 + 54143723 54143723 54143723 CGTCCAACGAGATCAAGGACAAGAGGCAGCTTATAGACAACCGCAAGCTCATTGAGACGGTAGGA CGTCCAACGAGATCAAGGACAAGAGGCAGCTTCTAGACAACCGCAAGCTCATTGAGACGGTAGGA A C CNOT3 Ensembl:ENSG00000088038 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54143672..54143768 26863196 MeRIP-seq:(Medium) rs587740207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1570764,Human_RBP_ID_1891603,Human_RBP_ID_9089577,Human_RBP_ID_9381373,Human_RBP_ID_13506214,Human_RBP_ID_18532631,Human_RBP_ID_18738912,Human_RBP_ID_26336754 Human_Splice_Rec_2042140,Human_Splice_Rec_2042141,Human_Splice_Rec_2042160,Human_Splice_Rec_2042190,Human_Splice_Rec_2042191,Human_Splice_Rec_2042224,Human_Splice_Rec_2042225,Human_Splice_Rec_2042250,Human_Splice_Rec_2042251,Human_Splice_Rec_2042280,Human_Splice_Rec_2042281,Human_Splice_Rec_2042307 Human_miRNA_ID_2894849 RMVar_hsa_circ_105088,RMVar_hsa_circ_122406,RMVar_hsa_circ_196221,RMVar_hsa_circ_196222,RMVar_hsa_circ_112357,RMVar_hsa_circ_196223,RMVar_hsa_circ_371364,RMVar_hsa_circ_196224 70651 RMVar_ID_70651 Human_SNP_ID_669685311 m1A Human chr19 + 54143723 54143723 54143723 CGTCCAACGAGATCAAGGACAAGAGGCAGCTTATAGACAACCGCAAGCTCATTGAGACGGTAGGA CGTCCAACGAGATCAAGGACAAGAGGCAGCTTGTAGACAACCGCAAGCTCATTGAGACGGTAGGA A G CNOT3 Ensembl:ENSG00000088038 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54143672..54143768 26863196 MeRIP-seq:(Medium) rs587740207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1570764,Human_RBP_ID_1891603,Human_RBP_ID_9089577,Human_RBP_ID_9381373,Human_RBP_ID_13506214,Human_RBP_ID_18532631,Human_RBP_ID_18738912,Human_RBP_ID_26336754 Human_Splice_Rec_2042140,Human_Splice_Rec_2042141,Human_Splice_Rec_2042160,Human_Splice_Rec_2042190,Human_Splice_Rec_2042191,Human_Splice_Rec_2042224,Human_Splice_Rec_2042225,Human_Splice_Rec_2042250,Human_Splice_Rec_2042251,Human_Splice_Rec_2042280,Human_Splice_Rec_2042281,Human_Splice_Rec_2042307 Human_miRNA_ID_2894849 RMVar_hsa_circ_105088,RMVar_hsa_circ_122406,RMVar_hsa_circ_196221,RMVar_hsa_circ_196222,RMVar_hsa_circ_112357,RMVar_hsa_circ_196223,RMVar_hsa_circ_371364,RMVar_hsa_circ_196224 70652 RMVar_ID_70652 Human_SNP_ID_669685604 m1A Human chr19 + 54144840 54144840 54144840 TCTAAAATCCGGGATTGTGGGGTATGAGTTCAAAGGGATACAAACTGTACAGACTTGCTGAAACC TCTAAAATCCGGGATTGTGGGGTATGAGTTCAGAGGGATACAAACTGTACAGACTTGCTGAAACC A G CNOT3 Ensembl:ENSG00000088038 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54144838..54145019 26863196 MeRIP-seq:(Medium) rs587708916 Functional Loss SNV dbSNP153 33..33 33 - - - 70653 RMVar_ID_70653 Human_SNP_ID_669686605 m1A Human chr19 + 54148204 54148204 54148204 CCTGTCCACAGCAACCAGCACCCTCAGTCCCCAGCTGTGCCGCCCACCTACCCCTCCGGCCCCCC CCTGTCCACAGCAACCAGCACCCTCAGTCCCCGGCTGTGCCGCCCACCTACCCCTCCGGCCCCCC A G CNOT3 Ensembl:ENSG00000088038 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:54148119..54148714;chr19:54148139..54148295 26863196 MeRIP-seq:(Medium) rs1468678130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3576167,Human_RBP_ID_9329184,Human_RBP_ID_27815653 Human_Splice_Rec_2042170,Human_Splice_Rec_2042202,Human_Splice_Rec_2042236,Human_Splice_Rec_2042262,Human_Splice_Rec_2042292,Human_Splice_Rec_2042318,Human_Splice_Rec_2042344 Human_miRNA_ID_465654,Human_miRNA_ID_843202,Human_miRNA_ID_875213,Human_miRNA_ID_1234002,Human_miRNA_ID_1358599,Human_miRNA_ID_1560853,Human_miRNA_ID_2686356,Human_miRNA_ID_2874281,Human_miRNA_ID_2982241,Human_miRNA_ID_3009945 70654 RMVar_ID_70654 Human_SNP_ID_669686692 m1A Human chr19 + 54148365 54148365 54148365 TCCCAGCCACAACTCGGGCACCCCTGCTCCCTATGCCCAGGCTGTGGCCCCACCAGCTCCCAGTG TCCCAGCCACAACTCGGGCACCCCTGCTCCCTGTGCCCAGGCTGTGGCCCCACCAGCTCCCAGTG A G CNOT3 Ensembl:ENSG00000088038 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54148230..54152296 32194978 MeRIP-seq:(Medium) rs1435025771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082622,Human_RBP_ID_17930765,Human_RBP_ID_26654968,Human_RBP_ID_27815654 70655 RMVar_ID_70655 Human_SNP_ID_669687338 m1A Human chr19 - 54149872 54149872 54149872 TGGAGAAAGAGCAAGTGTGAGAAGGGGACAGAAAGCCAGAGAGAGATCCAGAAAGAGGGTGGGGG TGGAGAAAGAGCAAGTGTGAGAAGGGGACAGAGAGCCAGAGAGAGATCCAGAAAGAGGGTGGGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54149870..54150045 26863196 MeRIP-seq:(Medium) rs1364858426 Functional Loss SNV dbSNP153 33..33 33 - - - 70656 RMVar_ID_70656 Human_SNP_ID_669688109 m1A Human chr19 - 54152209 54152209 54152209 TCAGAGGCTCAGGGGCCTGGGGAGGAAACAAGAGGCCTGGCCTGAGCACTTGGGCTGCAGGAGCA TCAGAGGCTCAGGGGCCTGGGGAGGAAACAAGGGGCCTGGCCTGAGCACTTGGGCTGCAGGAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54152205..54152286 26863196 MeRIP-seq:(Medium) rs1305071444 Functional Loss SNV dbSNP153 33..33 33 - - - 70657 RMVar_ID_70657 Human_SNP_ID_669688796 m1A Human chr19 - 54153858 54153856 54153858 GGACTCTACCCCAACCCTAGCAGCGGGAAGAGAGGGGGCGGGGCCCTCACCTGCTCAAACTCGTC GGACTCTACCCCAACCCTAGCAGCGGGAAGAG__GGGGCGGGGCCCTCACCTGCTCAAACTCGTC CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54153849..54154046 26863196 MeRIP-seq:(Medium) rs772685609 Functional Loss DEL dbSNP153 33..34 33 - - - 70658 RMVar_ID_70658 Human_SNP_ID_669688800 m1A Human chr19 - 54153858 54153858 54153858 GGACTCTACCCCAACCCTAGCAGCGGGAAGAGAGGGGGCGGGGCCCTCACCTGCTCAAACTCGTC GGACTCTACCCCAACCCTAGCAGCGGGAAGAGTGGGGGCGGGGCCCTCACCTGCTCAAACTCGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54153849..54154046 26863196 MeRIP-seq:(Medium) rs761391123 Functional Loss SNV dbSNP153 33..33 33 - - - 70659 RMVar_ID_70659 Human_SNP_ID_669688801 m1A Human chr19 - 54153858 54153858 54153858 GGACTCTACCCCAACCCTAGCAGCGGGAAGAGAGGGGGCGGGGCCCTCACCTGCTCAAACTCGTC GGACTCTACCCCAACCCTAGCAGCGGGAAGAGGGGGGGCGGGGCCCTCACCTGCTCAAACTCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54153849..54154046 26863196 MeRIP-seq:(Medium) rs761391123 Functional Loss SNV dbSNP153 33..33 33 - - - 70660 RMVar_ID_70660 Human_SNP_ID_669689328 m1A Human chr19 - 54155271 54155271 54155271 CGGGGGAGAAGGCGGTCAGTGAGTGGACGAGGAGGTGGTCTGGGATCTGGGCCGGACCAACAGAC CGGGGGAGAAGGCGGTCAGTGAGTGGACGAGGTGGTGGTCTGGGATCTGGGCCGGACCAACAGAC T A LENG1 Ensembl:ENSG00000105617 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54155269..54155409 26863196 MeRIP-seq:(Medium) rs199660083 Functional Loss SNV dbSNP153 33..33 33 - - - 70661 RMVar_ID_70661 Human_SNP_ID_669689552 m1A Human chr19 - 54155817 54155814 54155817 GGCCGGGCACTACAGGAGGGTCAGCCGGAAGAAGACGAGACGGATGACCGGCGGCGGCGGTACAA GGCCGGGCACTACAGGAGGGTCAGCCGGAAGA___CGAGACGGATGACCGGCGGCGGCGGTACAA GTCT G LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54155736..54155869 26863196 MeRIP-seq:(Medium) rs750292607 Functional Loss DEL dbSNP153 33..35 33 - - - 70662 RMVar_ID_70662 Human_SNP_ID_669689557 m1A Human chr19 - 54155817 54155817 54155817 GGCCGGGCACTACAGGAGGGTCAGCCGGAAGAAGACGAGACGGATGACCGGCGGCGGCGGTACAA GGCCGGGCACTACAGGAGGGTCAGCCGGAAGACGACGAGACGGATGACCGGCGGCGGCGGTACAA T G LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54155736..54155869 26863196 MeRIP-seq:(Medium) rs146921339 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70663 RMVar_ID_70663 Human_SNP_ID_669689924 m1A Human chr19 + 54156810 54156810 54156810 TTCTCAGACCCCTCCTTTTCCTTTCTGCTGCGACTGCCTTCATCACCGCCGTGCTGTCTCTTCTT TTCTCAGACCCCTCCTTTTCCTTTCTGCTGCGTCTGCCTTCATCACCGCCGTGCTGTCTCTTCTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54155806..54156977 26863196 MeRIP-seq:(Medium) rs150820847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23806704 70664 RMVar_ID_70664 Human_SNP_ID_669690486 m1A Human chr19 - 54158316 54158316 54158316 GCTGGAGGAAGGGAAAGGAGTGATCAGAGGCAATAAAGAGTACAAGGAAGAAAAGCGACAGGAGA GCTGGAGGAAGGGAAAGGAGTGATCAGAGGCAGTAAAGAGTACAAGGAAGAAAAGCGACAGGAGA T C LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54155806..54159633 32194978 MeRIP-seq:(Medium) rs147827510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2042395 70665 RMVar_ID_70665 Human_SNP_ID_669690487 m1A Human chr19 - 54158316 54158316 54158316 GCTGGAGGAAGGGAAAGGAGTGATCAGAGGCAATAAAGAGTACAAGGAAGAAAAGCGACAGGAGA GCTGGAGGAAGGGAAAGGAGTGATCAGAGGCACTAAAGAGTACAAGGAAGAAAAGCGACAGGAGA T G LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54155806..54159633 32194978 MeRIP-seq:(Medium) rs147827510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2042395 70666 RMVar_ID_70666 Human_SNP_ID_669690954 m1A Human chr19 - 54159655 54159655 54159655 CTTGCCCAAGAAGAGCTGGCACGTCCGGAACAAGGACAATGTCGCCCGCGTGCGGCGTGACGAGG CTTGCCCAAGAAGAGCTGGCACGTCCGGAACAGGGACAATGTCGCCCGCGTGCGGCGTGACGAGG T C LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:54158431..54159725;chr19:54155906..54159725 26863196 MeRIP-seq:(Medium) rs767943207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558734,Human_RBP_ID_26338237 Human_Splice_Rec_2042393 70667 RMVar_ID_70667 Human_SNP_ID_669696762 m1A Human chr19 + 54174030 54174030 54174030 TCACAGAATTCCCGGGACCAGCTGGCAGAGGGAGCGTCGTGACAGCTTACTCCTCCCGGAGCTTC TCACAGAATTCCCGGGACCAGCTGGCAGAGGGGGCGTCGTGACAGCTTACTCCTCCCGGAGCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54173980..54174155 26863196 MeRIP-seq:(Medium) rs1325587144 Functional Loss SNV dbSNP153 33..33 33 - - - 70668 RMVar_ID_70668 Human_SNP_ID_669696877 m1A Human chr19 + 54174211 54174211 54174211 GGAGGCCCAGTACCGAAGGGTGTCGGCCAAGGAGAGCAGCACGAAGCCCATGCACATGTAGTCAT GGAGGCCCAGTACCGAAGGGTGTCGGCCAAGGCGAGCAGCACGAAGCCCATGCACATGTAGTCAT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:54174160..54174261 32194978 MeRIP-seq:(Medium) rs754115048 Functional Loss SNV dbSNP153 33..33 33 - - - 70669 RMVar_ID_70669 Human_SNP_ID_669696894 m1A Human chr19 - 54174240 54174240 54174240 GGTGCACTGGTTCCTGAAGATGCGCGCCTATGACTACATGTGCATGGGCTTCGTGCTGCTCTCCT GGTGCACTGGTTCCTGAAGATGCGCGCCTATGTCTACATGTGCATGGGCTTCGTGCTGCTCTCCT T A MBOAT7 Ensembl:ENSG00000125505 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54174190..54174269 26863196 MeRIP-seq:(Medium) rs376095794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526625,Human_RBP_ID_2570005,Human_RBP_ID_5421818,Human_RBP_ID_17930788,Human_RBP_ID_22764805 Human_miRNA_ID_365218,Human_miRNA_ID_372430,Human_miRNA_ID_379600,Human_miRNA_ID_486372,Human_miRNA_ID_1240293,Human_miRNA_ID_1456069 70670 RMVar_ID_70670 Human_SNP_ID_669696982 m1A Human chr19 - 54174402 54174402 54174402 CAGGAGCGCCTGGACCATGCTGCTGAGCGCCTACTGGCACGGCCTCCACCCGGGCTACTACCTGA CAGGAGCGCCTGGACCATGCTGCTGAGCGCCTGCTGGCACGGCCTCCACCCGGGCTACTACCTGA T C MBOAT7 Ensembl:ENSG00000125505 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54174351..54174450 32194978 MeRIP-seq:(Medium) rs1361566280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330245,Human_RBP_ID_22447011,Human_RBP_ID_22742590,Human_RBP_ID_22763147 Human_Splice_Rec_2042518,Human_Splice_Rec_2042530,Human_Splice_Rec_2042540,Human_Splice_Rec_2042554,Human_Splice_Rec_2042556,Human_Splice_Rec_2042562 Human_miRNA_ID_1351554 70671 RMVar_ID_70671 Human_SNP_ID_669697082 m1A Human chr19 + 54174679 54174677 54174680 ACCAGACCCCACCTCCCTCCTCCCTCAGATCCAGGAGTCCAGACCCCACTTCCCTCCTCCCTCAG ACCAGACCCCACCTCCCTCCTCCCTCAGATC___GAGTCCAGACCCCACTTCCCTCCTCCCTCAG CCAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54174526..54174958 26863196 MeRIP-seq:(Medium) rs1216338726 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1570789,Human_RBP_ID_22975825 70672 RMVar_ID_70672 Human_SNP_ID_669699535 m1A Human chr19 + 54180911 54180911 54180911 TCCAGGCCACGTAGAAGCGCATGCGGAAGGCGAAGAAGACGGGGATCATGTAGAAGAGGCGGGCG TCCAGGCCACGTAGAAGCGCATGCGGAAGGCGGAGAAGACGGGGATCATGTAGAAGAGGCGGGCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:54180860..54181061 32194978 MeRIP-seq:(Medium) rs745441950 Functional Loss SNV dbSNP153 33..33 33 - - - 70673 RMVar_ID_70673 Human_SNP_ID_669699543 m1A Human chr19 - 54180929 54180929 54180929 CTACGCCCGCCCGCTGCCCGCCCGCCTCTTCTACATGATCCCCGTCTTCTTCGCCTTCCGCATGC CTACGCCCGCCCGCTGCCCGCCCGCCTCTTCTGCATGATCCCCGTCTTCTTCGCCTTCCGCATGC T C MBOAT7 Ensembl:ENSG00000125505 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54180710..54181111 26863196 MeRIP-seq:(Medium) rs544377469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18947316,Human_RBP_ID_22071713,Human_RBP_ID_27471186 Human_miRNA_ID_2710205 70674 RMVar_ID_70674 Human_SNP_ID_669699583 m1A Human chr19 + 54181000 54181000 54181000 TCCTCGCGCACGGCCTCCAGCGGGAAGAGGTGAGAGGAGAGCAGGAACAGCAGGCCGAAGAGCGG TCCTCGCGCACGGCCTCCAGCGGGAAGAGGTGCGAGGAGAGCAGGAACAGCAGGCCGAAGAGCGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54180810..54186972 32194978 MeRIP-seq:(Medium) rs1244489257 Functional Loss SNV dbSNP153 33..33 33 - - - 70675 RMVar_ID_70675 Human_SNP_ID_669700512 m1A Human chr19 + 54183487 54183487 54183487 AGGCACTCAGGGCGGAAGGGGACACAGGAGACAGAGCGGCAGAGTTGTTAGGGCAGCCCCACTCA AGGCACTCAGGGCGGAAGGGGACACAGGAGACGGAGCGGCAGAGTTGTTAGGGCAGCCCCACTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54183484..54183625 26863196 MeRIP-seq:(Medium) rs1163535250 Functional Loss SNV dbSNP153 33..33 33 - - - 70676 RMVar_ID_70676 Human_SNP_ID_669702260 m1A Human chr19 - 54188299 54188299 54188299 GATGGGGAGCAGCCGCTGTGGGCCTGGGGCTCACCCTGTTCACCTGTGGCCCCCACACTTTGCAT GATGGGGAGCAGCCGCTGTGGGCCTGGGGCTCTCCCTGTTCACCTGTGGCCCCCACACTTTGCAT T A MBOAT7 Ensembl:ENSG00000125505 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54188251..54188300 26863196 MeRIP-seq:(Medium) rs201366800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239999,Human_RBP_ID_4546390,Human_RBP_ID_18470657,Human_RBP_ID_18995395,Human_RBP_ID_22448003 Human_Splice_Rec_2042510,Human_Splice_Rec_2042511,Human_Splice_Rec_2042522,Human_Splice_Rec_2042523,Human_Splice_Rec_2042532,Human_Splice_Rec_2042533,Human_Splice_Rec_2042544,Human_Splice_Rec_2042545,Human_Splice_Rec_2042557,Human_Splice_Rec_2042566,Human_Splice_Rec_2042567,Human_Splice_Rec_2042580,Human_Splice_Rec_2042581,Human_Splice_Rec_2042590,Human_Splice_Rec_2042591,Human_Splice_Rec_2042597,Human_Splice_Rec_2042604,Human_Splice_Rec_2042605,Human_Splice_Rec_2042612,Human_Splice_Rec_2042613,Human_Splice_Rec_2042618,Human_Splice_Rec_2042619 Human_miRNA_ID_2891270 70677 RMVar_ID_70677 Human_SNP_ID_669702261 m1A Human chr19 - 54188299 54188299 54188299 GATGGGGAGCAGCCGCTGTGGGCCTGGGGCTCACCCTGTTCACCTGTGGCCCCCACACTTTGCAT GATGGGGAGCAGCCGCTGTGGGCCTGGGGCTCCCCCTGTTCACCTGTGGCCCCCACACTTTGCAT T G MBOAT7 Ensembl:ENSG00000125505 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54188251..54188300 26863196 MeRIP-seq:(Medium) rs201366800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239999,Human_RBP_ID_4546390,Human_RBP_ID_18470657,Human_RBP_ID_18995395,Human_RBP_ID_22448003 Human_Splice_Rec_2042510,Human_Splice_Rec_2042511,Human_Splice_Rec_2042522,Human_Splice_Rec_2042523,Human_Splice_Rec_2042532,Human_Splice_Rec_2042533,Human_Splice_Rec_2042544,Human_Splice_Rec_2042545,Human_Splice_Rec_2042557,Human_Splice_Rec_2042566,Human_Splice_Rec_2042567,Human_Splice_Rec_2042580,Human_Splice_Rec_2042581,Human_Splice_Rec_2042590,Human_Splice_Rec_2042591,Human_Splice_Rec_2042597,Human_Splice_Rec_2042604,Human_Splice_Rec_2042605,Human_Splice_Rec_2042612,Human_Splice_Rec_2042613,Human_Splice_Rec_2042618,Human_Splice_Rec_2042619 Human_miRNA_ID_2891270 70678 RMVar_ID_70678 Human_SNP_ID_669702993 m1A Human chr19 - 54190347 54190347 54190347 CGAGTCACCTCATAAACAGTAATTCGCAGTCGAGGTGGAGCCACCCACTGCGCACCGCGCCACGC CGAGTCACCTCATAAACAGTAATTCGCAGTCGCGGTGGAGCCACCCACTGCGCACCGCGCCACGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54190296..54190502 26863196 MeRIP-seq:(Medium) rs1158808096 Functional Loss SNV dbSNP153 33..33 33 - - - 70679 RMVar_ID_70679 Human_SNP_ID_669703031 m1A Human chr19 + 54190413 54190413 54190413 TGGTTCTATCGGTGGACAGTGGGACATTCTGAAGGGAGGCAAGGAGGCGGACTGAGCGCTCCCAA TGGTTCTATCGGTGGACAGTGGGACATTCTGAGGGGAGGCAAGGAGGCGGACTGAGCGCTCCCAA A G TSEN34 Ensembl:ENSG00000170892 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54190136..54190492 26863196 MeRIP-seq:(Medium) rs1428209921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22594470 Human_Splice_Rec_2042633 70680 RMVar_ID_70680 Human_SNP_ID_669703769 m1A Human chr19 + 54191826 54191826 54191826 AGACCCGTCGTCAGGAGCTCCTGGAGAAGATTACGGAGGGCCAGGCTGCTAAGAAGCAGAAACTA AGACCCGTCGTCAGGAGCTCCTGGAGAAGATTGCGGAGGGCCAGGCTGCTAAGAAGCAGAAACTA A G TSEN34 Ensembl:ENSG00000170892 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54191778..54191916 26863196 MeRIP-seq:(Medium) rs1162008968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4546450,Human_RBP_ID_23806725 70681 RMVar_ID_70681 Human_SNP_ID_669704045 m1A Human chr19 - 54192359 54192359 54192359 GCCCCAACCCATACTCACCAGGATAGACCAGGAAGTCACCTCCGAACTTGCCAGCCGCACTGAGG GCCCCAACCCATACTCACCAGGATAGACCAGGGAGTCACCTCCGAACTTGCCAGCCGCACTGAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54191339..54193450 32194978 MeRIP-seq:(Medium) rs1190345103 Functional Loss SNV dbSNP153 33..33 33 - - - 70682 RMVar_ID_70682 Human_SNP_ID_669707383 m1A Human chr19 - 54200886 54200882 54200887 CTAGAGAAAAAGCACACCACCGCACCTCACCTAAGCAAACCACCCGGTCACTGAGAAAGAGGCGC CTAGAGAAAAAGCACACCACCGCACCTCACC_____AAACCACCCGGTCACTGAGAAAGAGGCGC TGCTTA T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54200851..54200925 26863410 MeRIP-seq:(Medium) rs1428128523 Functional Loss DEL dbSNP153 32..36 33 - - - 70683 RMVar_ID_70683 Human_SNP_ID_669707392 m1A Human chr19 - 54200890 54200890 54200890 AACCCTAGAGAAAAAGCACACCACCGCACCTCACCTAAGCAAACCACCCGGTCACTGAGAAAGAG AACCCTAGAGAAAAAGCACACCACCGCACCTCGCCTAAGCAAACCACCCGGTCACTGAGAAAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEPG2 cell line,mRNA heat shock 4h chr19:54200851..54201041;chr19:54200851..54200925;chr19:54200876..54200925;chr19:54200851..54201021 26863196,26863410,26863410,26863196 MeRIP-seq:(Medium) rs1165202493 Functional Loss SNV dbSNP153 33..33 33 - - - 70684 RMVar_ID_70684 Human_SNP_ID_669707547 m1A Human chr19 + 54201158 54201158 54201158 GGATCCCTTACGCTCACACTTCTCTCCCGCGCAGGCGCAGACGGGGAAGCGGAGCCAACATGCCA GGATCCCTTACGCTCACACTTCTCTCCCGCGCCGGCGCAGACGGGGAAGCGGAGCCAACATGCCA A C RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:54201151..54201200 26863196 MeRIP-seq:(Medium) rs966706509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54506,Human_RBP_ID_825134,Human_RBP_ID_912682,Human_RBP_ID_4546492,Human_RBP_ID_5117598,Human_RBP_ID_5145416,Human_RBP_ID_9089587,Human_RBP_ID_18421596,Human_RBP_ID_22449018 Human_miRNA_ID_2250386 RMVar_hsa_circ_82720,RMVar_hsa_circ_98996,RMVar_hsa_circ_103392,RMVar_hsa_circ_196226 70685 RMVar_ID_70685 Human_SNP_ID_669707548 m1A Human chr19 + 54201158 54201158 54201158 GGATCCCTTACGCTCACACTTCTCTCCCGCGCAGGCGCAGACGGGGAAGCGGAGCCAACATGCCA GGATCCCTTACGCTCACACTTCTCTCCCGCGCGGGCGCAGACGGGGAAGCGGAGCCAACATGCCA A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:54201151..54201200 26863196 MeRIP-seq:(Medium) rs966706509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54506,Human_RBP_ID_825134,Human_RBP_ID_912682,Human_RBP_ID_4546492,Human_RBP_ID_5117598,Human_RBP_ID_5145416,Human_RBP_ID_9089587,Human_RBP_ID_18421596,Human_RBP_ID_22449018 Human_miRNA_ID_2250386 RMVar_hsa_circ_82720,RMVar_hsa_circ_98996,RMVar_hsa_circ_103392,RMVar_hsa_circ_196226 70686 RMVar_ID_70686 Human_SNP_ID_669707571 m1A Human chr19 + 54201183 54201183 54201183 CCCGCGCAGGCGCAGACGGGGAAGCGGAGCCAACATGCCAGTGGCCCGGAGCTGGGTTTGTCGCA CCCGCGCAGGCGCAGACGGGGAAGCGGAGCCACCATGCCAGTGGCCCGGAGCTGGGTTTGTCGCA A C RPS9 Ensembl:ENSG00000170889 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54201161..54201272 26863410 MeRIP-seq:(Medium) rs141881269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240594,Human_RBP_ID_526690,Human_RBP_ID_772029,Human_RBP_ID_912682,Human_RBP_ID_4546492,Human_RBP_ID_5116418,Human_RBP_ID_5145416,Human_RBP_ID_17656361,Human_RBP_ID_18421596,Human_RBP_ID_22449018,Human_RBP_ID_26995060,Human_RBP_ID_27278128 Human_Splice_Rec_2042694,Human_Splice_Rec_2042695,Human_Splice_Rec_2042700,Human_Splice_Rec_2042701,Human_Splice_Rec_2042708,Human_Splice_Rec_2042709,Human_Splice_Rec_2042716,Human_Splice_Rec_2042717,Human_Splice_Rec_2042724,Human_Splice_Rec_2042725,Human_Splice_Rec_2042734,Human_Splice_Rec_2042735,Human_Splice_Rec_2042742,Human_Splice_Rec_2042743,Human_Splice_Rec_2042750,Human_Splice_Rec_2042751,Human_Splice_Rec_2042760,Human_Splice_Rec_2042761,Human_Splice_Rec_2042766,Human_Splice_Rec_2042767,Human_Splice_Rec_2042773,Human_Splice_Rec_2042779,Human_Splice_Rec_2042781 RMVar_hsa_circ_82720,RMVar_hsa_circ_98996,RMVar_hsa_circ_103392,RMVar_hsa_circ_196226,RMVar_hsa_circ_196227,RMVar_hsa_circ_196228 70687 RMVar_ID_70687 Human_SNP_ID_669707572 m1A Human chr19 + 54201183 54201183 54201183 CCCGCGCAGGCGCAGACGGGGAAGCGGAGCCAACATGCCAGTGGCCCGGAGCTGGGTTTGTCGCA CCCGCGCAGGCGCAGACGGGGAAGCGGAGCCAGCATGCCAGTGGCCCGGAGCTGGGTTTGTCGCA A G RPS9 Ensembl:ENSG00000170889 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54201161..54201272 26863410 MeRIP-seq:(Medium) rs141881269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240594,Human_RBP_ID_526690,Human_RBP_ID_772029,Human_RBP_ID_912682,Human_RBP_ID_4546492,Human_RBP_ID_5116418,Human_RBP_ID_5145416,Human_RBP_ID_17656361,Human_RBP_ID_18421596,Human_RBP_ID_22449018,Human_RBP_ID_26995060,Human_RBP_ID_27278128 Human_Splice_Rec_2042694,Human_Splice_Rec_2042695,Human_Splice_Rec_2042700,Human_Splice_Rec_2042701,Human_Splice_Rec_2042708,Human_Splice_Rec_2042709,Human_Splice_Rec_2042716,Human_Splice_Rec_2042717,Human_Splice_Rec_2042724,Human_Splice_Rec_2042725,Human_Splice_Rec_2042734,Human_Splice_Rec_2042735,Human_Splice_Rec_2042742,Human_Splice_Rec_2042743,Human_Splice_Rec_2042750,Human_Splice_Rec_2042751,Human_Splice_Rec_2042760,Human_Splice_Rec_2042761,Human_Splice_Rec_2042766,Human_Splice_Rec_2042767,Human_Splice_Rec_2042773,Human_Splice_Rec_2042779,Human_Splice_Rec_2042781 RMVar_hsa_circ_82720,RMVar_hsa_circ_98996,RMVar_hsa_circ_103392,RMVar_hsa_circ_196226,RMVar_hsa_circ_196227,RMVar_hsa_circ_196228 70688 RMVar_ID_70688 Human_SNP_ID_669707596 m1A Human chr19 - 54201258 54201258 54201258 GCCACTCACCGATCAGCTTCAGCTCTTGGTCGAGACGAGATTTCTCGAAGGGTCTCCGCGGGGTC GCCACTCACCGATCAGCTTCAGCTCTTGGTCGCGACGAGATTTCTCGAAGGGTCTCCGCGGGGTC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:54201151..54201325 26863410 MeRIP-seq:(Medium) rs928989934 Functional Loss SNV dbSNP153 33..33 33 - - - 70689 RMVar_ID_70689 Human_SNP_ID_669707688 m1A Human chr19 - 54201447 54201447 54201447 GGAGAAGGGGGTGGACAAGTGTAGTCCCACGTACTGGCACAACAACTAGACTGGCAGCTTTGGAA GGAGAAGGGGGTGGACAAGTGTAGTCCCACGTCCTGGCACAACAACTAGACTGGCAGCTTTGGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54201444..54201655 26863196 MeRIP-seq:(Medium) rs1161783667 Functional Loss SNV dbSNP153 33..33 33 - - - 70690 RMVar_ID_70690 Human_SNP_ID_669707757 m1A Human chr19 + 54201586 54201586 54201586 GGCCGCCCGGGAACTGCTGACGCTTGATGAGAAGGACCCACGGCGTCTGTTCGAAGGTGCGTATG GGCCGCCCGGGAACTGCTGACGCTTGATGAGAGGGACCCACGGCGTCTGTTCGAAGGTGCGTATG A G RPS9 Ensembl:ENSG00000170889 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54201435..54201650;chr19:54201476..54201600 26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs552278556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526695,Human_RBP_ID_824829,Human_RBP_ID_18192488 Human_Splice_Rec_2042696,Human_Splice_Rec_2042697,Human_Splice_Rec_2042702,Human_Splice_Rec_2042703,Human_Splice_Rec_2042710,Human_Splice_Rec_2042711,Human_Splice_Rec_2042718,Human_Splice_Rec_2042719,Human_Splice_Rec_2042726,Human_Splice_Rec_2042727,Human_Splice_Rec_2042736,Human_Splice_Rec_2042737,Human_Splice_Rec_2042744,Human_Splice_Rec_2042745,Human_Splice_Rec_2042752,Human_Splice_Rec_2042753,Human_Splice_Rec_2042762,Human_Splice_Rec_2042763,Human_Splice_Rec_2042768,Human_Splice_Rec_2042769,Human_Splice_Rec_2042774,Human_Splice_Rec_2042775,Human_Splice_Rec_2042780,Human_Splice_Rec_2042782,Human_Splice_Rec_2042783 RMVar_hsa_circ_82720,RMVar_hsa_circ_98996,RMVar_hsa_circ_103392,RMVar_hsa_circ_196226,RMVar_hsa_circ_196227,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 70691 RMVar_ID_70691 Human_SNP_ID_669783020 m1A Human chr19 - 54431258 54431258 54431258 GGCGCAATGGCAGGGGTCCAAGGAGAAGGAGGAGGTAGTTCTGTGGGTCGAGACAGAGGCCCCCC GGCGCAATGGCAGGGGTCCAAGGAGAAGGAGGGGGTAGTTCTGTGGGTCGAGACAGAGGCCCCCC T C AC245884.1 Ensembl:ENSG00000227407 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54431208..54431414 26863196 MeRIP-seq:(Medium) rs1250361484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587793,Human_RBP_ID_8196857 70692 RMVar_ID_70692 Human_SNP_ID_669784096 m1A Human chr19 - 54435121 54435121 54435121 CTGCTACTTCCGTTTCCCTTCTCCCTCCCGGCAGCGGCACCTCCTGCAAGAGCATCCTCCCCTGC CTGCTACTTCCGTTTCCCTTCTCCCTCCCGGCTGCGGCACCTCCTGCAAGAGCATCCTCCCCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54435115..54435200 26863196 MeRIP-seq:(Medium) rs951617060 Functional Loss SNV dbSNP153 33..33 33 - - - 70693 RMVar_ID_70693 Human_SNP_ID_669784627 m1A Human chr19 - 54436307 54436307 54436307 GAAGGAACTGCGGAGAGAGGGAGAGACAGGGCAGTGATGCAGGCTGGAGGGCCTGCCCGGTGCGA GAAGGAACTGCGGAGAGAGGGAGAGACAGGGCGGTGATGCAGGCTGGAGGGCCTGCCCGGTGCGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:54436259..54436394 26863196 MeRIP-seq:(Medium) rs959768005 Functional Loss SNV dbSNP153 33..33 33 - - - 70694 RMVar_ID_70694 Human_SNP_ID_669788266 m1A Human chr19 + 54448341 54448341 54448341 GACCTTCGGGGGTCTGCTCCGCGCCCACCCTTACACATCTGTGACCCCACACACTTCCACCCCAG GACCTTCGGGGGTCTGCTCCGCGCCCACCCTTTCACATCTGTGACCCCACACACTTCCACCCCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54448291..54448591 26863196 MeRIP-seq:(Medium) rs1174392456 Functional Loss SNV dbSNP153 33..33 33 - - - 70695 RMVar_ID_70695 Human_SNP_ID_669788550 m1A Human chr19 + 54449262 54449262 54449262 GGTGGCACAGCGGTGTCGTGGCCGTGTTGCTGATCGCCTGGGTGGTTGTTGGCGTGTCCCTGCAG GGTGGCACAGCGGTGTCGTGGCCGTGTTGCTGGTCGCCTGGGTGGTTGTTGGCGTGTCCCTGCAG A G LENG8 Ensembl:ENSG00000167615 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:54449201..54449351 26863196 MeRIP-seq:(Medium) rs1181047366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3576236,Human_RBP_ID_4558747,Human_RBP_ID_8493530,Human_RBP_ID_8837143,Human_RBP_ID_23806832,Human_RBP_ID_27815659 Human_Splice_Rec_2043777,Human_Splice_Rec_2043803,Human_Splice_Rec_2043833,Human_Splice_Rec_2043847,Human_Splice_Rec_2043873 70696 RMVar_ID_70696 Human_SNP_ID_669788565 m1A Human chr19 - 54449302 54449302 54449302 CTGCTCGCCTGCCGCTCCCCTTACCAACCAGGATCCTTCGCTGCAGGGACACGCCAACAACCACC CTGCTCGCCTGCCGCTCCCCTTACCAACCAGGGTCCTTCGCTGCAGGGACACGCCAACAACCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54449251..54449325 32194978 MeRIP-seq:(Medium) rs1011512616 Functional Loss SNV dbSNP153 33..33 33 - - - 70697 RMVar_ID_70697 Human_SNP_ID_669789306 m1A Human chr19 - 54451206 54451206 54451206 TCACAAAGTGGGGAAGAAAAGTAGATGGACTCAAGAGAAGCCGGGCAGAAAAGGGGAGGCTGACT TCACAAAGTGGGGAAGAAAAGTAGATGGACTCTAGAGAAGCCGGGCAGAAAAGGGGAGGCTGACT T A lnc-LENG9-4 RNACentral:URS00008C268E lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:54451204..54451350 26863196 MeRIP-seq:(Medium) rs1243378966 Functional Loss SNV dbSNP153 33..33 33 - - - 70698 RMVar_ID_70698 Human_SNP_ID_669789346 m1A Human chr19 - 54451340 54451340 54451340 TACGTTGATCACCCACGTTGGCCGCCATCTGGACCTTGGGGTATAAGGGGTGGACCTCGGGAGCC TACGTTGATCACCCACGTTGGCCGCCATCTGGTCCTTGGGGTATAAGGGGTGGACCTCGGGAGCC T A lnc-LENG9-4 RNACentral:URS00008C268E lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:54451242..54451426;chr19:54451258..54451400;chr19:54451250..54451439;chr19:54451276..54451400 26863196 MeRIP-seq:(Medium) rs775705465 Functional Loss SNV dbSNP153 33..33 33 - - - 70699 RMVar_ID_70699 Human_SNP_ID_669789782 m1A Human chr19 + 54452682 54452679 54452682 GTACGTGTCCCAGGCAGAAGCCTCAGCTTTGCAGCAGCAGCAGTACTACCAGTGGTACCAGCAGT GTACGTGTCCCAGGCAGAAGCCTCAGCTTT___GCAGCAGCAGTACTACCAGTGGTACCAGCAGT TGCA T LENG8 Ensembl:ENSG00000167615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54452076..54452725 32194978 MeRIP-seq:(Medium) rs1329533675 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_54413,Human_RBP_ID_279911,Human_RBP_ID_911958,Human_RBP_ID_1891660,Human_RBP_ID_3957478,Human_RBP_ID_26338240,Human_RBP_ID_27815662 Human_Splice_Rec_2043782,Human_Splice_Rec_2043783,Human_Splice_Rec_2043808,Human_Splice_Rec_2043809,Human_Splice_Rec_2043838,Human_Splice_Rec_2043839,Human_Splice_Rec_2043852,Human_Splice_Rec_2043853,Human_Splice_Rec_2043876,Human_Splice_Rec_2043882,Human_Splice_Rec_2043886,Human_Splice_Rec_2043887,Human_Splice_Rec_2043910,Human_Splice_Rec_2043911 Human_miRNA_ID_1993995 RMVar_hsa_circ_28542,RMVar_hsa_circ_88741,RMVar_hsa_circ_196237 70700 RMVar_ID_70700 Human_SNP_ID_669789785 m1A Human chr19 + 54452682 54452682 54452682 GTACGTGTCCCAGGCAGAAGCCTCAGCTTTGCAGCAGCAGCAGTACTACCAGTGGTACCAGCAGT GTACGTGTCCCAGGCAGAAGCCTCAGCTTTGCGGCAGCAGCAGTACTACCAGTGGTACCAGCAGT A G LENG8 Ensembl:ENSG00000167615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54452076..54452725 32194978 MeRIP-seq:(Medium) rs1033583489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54413,Human_RBP_ID_279911,Human_RBP_ID_911958,Human_RBP_ID_1891660,Human_RBP_ID_3957478,Human_RBP_ID_26338240,Human_RBP_ID_27815662 Human_Splice_Rec_2043782,Human_Splice_Rec_2043783,Human_Splice_Rec_2043808,Human_Splice_Rec_2043809,Human_Splice_Rec_2043838,Human_Splice_Rec_2043839,Human_Splice_Rec_2043852,Human_Splice_Rec_2043853,Human_Splice_Rec_2043876,Human_Splice_Rec_2043882,Human_Splice_Rec_2043886,Human_Splice_Rec_2043887,Human_Splice_Rec_2043910,Human_Splice_Rec_2043911 Human_miRNA_ID_1993995 RMVar_hsa_circ_28542,RMVar_hsa_circ_88741,RMVar_hsa_circ_196237 70701 RMVar_ID_70701 Human_SNP_ID_669789786 m1A Human chr19 + 54452682 54452682 54452682 GTACGTGTCCCAGGCAGAAGCCTCAGCTTTGCAGCAGCAGCAGTACTACCAGTGGTACCAGCAGT GTACGTGTCCCAGGCAGAAGCCTCAGCTTTGCTGCAGCAGCAGTACTACCAGTGGTACCAGCAGT A T LENG8 Ensembl:ENSG00000167615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54452076..54452725 32194978 MeRIP-seq:(Medium) rs1033583489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54413,Human_RBP_ID_279911,Human_RBP_ID_911958,Human_RBP_ID_1891660,Human_RBP_ID_3957478,Human_RBP_ID_26338240,Human_RBP_ID_27815662 Human_Splice_Rec_2043782,Human_Splice_Rec_2043783,Human_Splice_Rec_2043808,Human_Splice_Rec_2043809,Human_Splice_Rec_2043838,Human_Splice_Rec_2043839,Human_Splice_Rec_2043852,Human_Splice_Rec_2043853,Human_Splice_Rec_2043876,Human_Splice_Rec_2043882,Human_Splice_Rec_2043886,Human_Splice_Rec_2043887,Human_Splice_Rec_2043910,Human_Splice_Rec_2043911 Human_miRNA_ID_1993995 RMVar_hsa_circ_28542,RMVar_hsa_circ_88741,RMVar_hsa_circ_196237 70702 RMVar_ID_70702 Human_SNP_ID_669790386 m1A Human chr19 + 54454497 54454471 54454498 CCAGGCTCCCCCTCAGCAGCTGCCGTCGGCTCAGCCCCCTCAGCCCTCAAATCCCCCACATGGGG CCAGGCT___________________________CCCCCTCAGCCCTCAAATCCCCCACATGGGG TCCCCCTCAGCAGCTGCCGTCGGCTCAG T LENG8 Ensembl:ENSG00000167615 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:54454384..54454612;chr19:54454451..54454650 26863196 MeRIP-seq:(Medium) rs779216885 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_280204,Human_RBP_ID_3957483,Human_RBP_ID_13507704,Human_RBP_ID_18739023,Human_RBP_ID_22975872 Human_Splice_Rec_2043784,Human_Splice_Rec_2043812,Human_Splice_Rec_2043842,Human_Splice_Rec_2043854,Human_Splice_Rec_2043890 70703 RMVar_ID_70703 Human_SNP_ID_669792285 m1A Human chr19 - 54458594 54458594 54458594 GGGTTGGGGGCTGGGGGAGGCCTGCGGCCAGGAGCTGGTCTGAGGGGCGGTGCGAGGCGGAAGGA GGGTTGGGGGCTGGGGGAGGCCTGCGGCCAGGGGCTGGTCTGAGGGGCGGTGCGAGGCGGAAGGA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54458495..54458775 26863410 MeRIP-seq:(Medium) rs777900569 Functional Loss SNV dbSNP153 33..33 33 - - - 70704 RMVar_ID_70704 Human_SNP_ID_669792301 m1A Human chr19 + 54458623 54458623 54458623 AGCTCCTGGCCGCAGGCCTCCCCCAGCCCCCAACCCTTGTCCTGGTCCTTGCTTCCCCATCATCT AGCTCCTGGCCGCAGGCCTCCCCCAGCCCCCACCCCTTGTCCTGGTCCTTGCTTCCCCATCATCT A C LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:54458574..54458844 26863196 MeRIP-seq:(Medium) rs569099002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082050,Human_RBP_ID_18945944,Human_RBP_ID_20349691,Human_RBP_ID_22426378,Human_RBP_ID_22812123,Human_RBP_ID_22975909 70705 RMVar_ID_70705 Human_SNP_ID_669792302 m1A Human chr19 + 54458623 54458623 54458623 AGCTCCTGGCCGCAGGCCTCCCCCAGCCCCCAACCCTTGTCCTGGTCCTTGCTTCCCCATCATCT AGCTCCTGGCCGCAGGCCTCCCCCAGCCCCCAGCCCTTGTCCTGGTCCTTGCTTCCCCATCATCT A G LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:54458574..54458844 26863196 MeRIP-seq:(Medium) rs569099002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082050,Human_RBP_ID_18945944,Human_RBP_ID_20349691,Human_RBP_ID_22426378,Human_RBP_ID_22812123,Human_RBP_ID_22975909 70706 RMVar_ID_70706 Human_SNP_ID_669792310 m1A Human chr19 - 54458636 54458636 54458636 GCTGAATGGAGAAAGATGATGGGGAAGCAAGGACCAGGACAAGGGTTGGGGGCTGGGGGAGGCCT GCTGAATGGAGAAAGATGATGGGGAAGCAAGGTCCAGGACAAGGGTTGGGGGCTGGGGGAGGCCT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:54458537..54458925 26863196 MeRIP-seq:(Medium) rs974585957 Functional Loss SNV dbSNP153 33..33 33 - - - 70707 RMVar_ID_70707 Human_SNP_ID_669792888 m1A Human chr19 + 54460202 54460202 54460202 CACTCGGTGCCTGGGTTCCTGTGTGTGTGGAAAGGGTAGGGCTGCACCCTGTGGAAGAGGGTTCA CACTCGGTGCCTGGGTTCCTGTGTGTGTGGAAGGGGTAGGGCTGCACCCTGTGGAAGAGGGTTCA A G LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54460153..54460471 26863196 MeRIP-seq:(Medium) rs569111640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2570150,Human_RBP_ID_3576257,Human_RBP_ID_3957505,Human_RBP_ID_6783510,Human_RBP_ID_8493566,Human_RBP_ID_13507845,Human_RBP_ID_17132019,Human_RBP_ID_22592538,Human_RBP_ID_22665942,Human_RBP_ID_22812154,Human_RBP_ID_23806889,Human_RBP_ID_26995187,Human_RBP_ID_27682667,Human_RBP_ID_27839650 70708 RMVar_ID_70708 Human_SNP_ID_669793119 m1A Human chr19 - 54460723 54460723 54460723 AAGAGGAGAAGGTGATGAGGCGGGCGGGCGGGAGGGCAGGGGAGGGCCCCACGAGCGGGGAGGCC AAGAGGAGAAGGTGATGAGGCGGGCGGGCGGGGGGGCAGGGGAGGGCCCCACGAGCGGGGAGGCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54460640..54460727 26863410 MeRIP-seq:(Medium) rs940200417 Functional Loss SNV dbSNP153 33..33 33 - - - 70709 RMVar_ID_70709 Human_SNP_ID_669793419 m1A Human chr19 + 54461268 54461268 54461268 CTCTCTCTTTCGAGCTTGCACTCCGGTACCCGACCCGGCGCCCTGGCCCATCCCATGCCGGGGGG CTCTCTCTTTCGAGCTTGCACTCCGGTACCCGTCCCGGCGCCCTGGCCCATCCCATGCCGGGGGG A T LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54461226..54461375 32194978 MeRIP-seq:(Medium) rs1411576958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55511,Human_RBP_ID_526760,Human_RBP_ID_772771,Human_RBP_ID_1570941,Human_RBP_ID_5117113,Human_RBP_ID_5145884,Human_RBP_ID_8256339,Human_RBP_ID_13507909,Human_RBP_ID_18166458,Human_RBP_ID_18739087,Human_RBP_ID_22070546,Human_RBP_ID_22663183,Human_RBP_ID_24559722,Human_RBP_ID_25440859,Human_RBP_ID_27839656 Human_Splice_Rec_2043914 70710 RMVar_ID_70710 Human_SNP_ID_669793559 m1A Human chr19 - 54461489 54461489 54461489 GCGGCGGAGGATCTGGTGCTGGTGGTGCTGGCACTTCAGGGTGGGGGGCCGAGGACGGGCACAGT GCGGCGGAGGATCTGGTGCTGGTGGTGCTGGCGCTTCAGGGTGGGGGGCCGAGGACGGGCACAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:54461019..54461825 26863196 MeRIP-seq:(Medium) rs757074374 Functional Loss SNV dbSNP153 33..33 33 - - - 70711 RMVar_ID_70711 Human_SNP_ID_669793563 m1A Human chr19 + 54461493 54461493 54461493 TGCCCGTCCTCGGCCCCCCACCCTGAAGTGCCAGCACCACCAGCACCAGATCCTCCGCCGCCACA TGCCCGTCCTCGGCCCCCCACCCTGAAGTGCCGGCACCACCAGCACCAGATCCTCCGCCGCCACA A G LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:54460662..54461956;chr19:54461058..54461850 26863196 MeRIP-seq:(Medium) rs1242645555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241785,Human_RBP_ID_13507921,Human_RBP_ID_22070553,Human_RBP_ID_22239018,Human_RBP_ID_23114829 70712 RMVar_ID_70712 Human_SNP_ID_669793570 m1A Human chr19 - 54461511 54461511 54461511 GGCGTGTCCTCAGTGCGGTGTGGCGGCGGAGGATCTGGTGCTGGTGGTGCTGGCACTTCAGGGTG GGCGTGTCCTCAGTGCGGTGTGGCGGCGGAGGTTCTGGTGCTGGTGGTGCTGGCACTTCAGGGTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:54461284..54461639 26863196 MeRIP-seq:(Medium) rs1027832797 Functional Loss SNV dbSNP153 33..33 33 - - - 70713 RMVar_ID_70713 Human_SNP_ID_669793684 m1A Human chr19 - 54461698 54461690 54461698 ATGACGTGAGCTGGTGATCCATGAAGGCAGGGAGGGAGGGGAACCGTTTTACCTGTGCTGAACCA ATGACGTGAGCTGGTGATCCATGAAGGCAGGG________GAACCGTTTTACCTGTGCTGAACCA CCCCTCCCT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:54461676..54461700 26863196 MeRIP-seq:(Medium) rs771804093 Functional Loss DEL dbSNP153 33..40 33 - - - 70714 RMVar_ID_70714 Human_SNP_ID_669794437 m1A Human chr19 + 54462817 54462817 54462817 TGGTGGCTGCTGTTGGCTTCAGTGCCTCAGTCACTCCGGCGAGGCGTCCTCTTGGGGCCAGTGTT TGGTGGCTGCTGTTGGCTTCAGTGCCTCAGTCGCTCCGGCGAGGCGTCCTCTTGGGGCCAGTGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54462780..54462859 26863196 MeRIP-seq:(Medium) rs1437363586 Functional Loss SNV dbSNP153 33..33 33 - - - 70715 RMVar_ID_70715 Human_SNP_ID_669794880 m1A Human chr19 - 54463637 54463637 54463637 GGCACGCGGCGTGGTCCCCAGAGCTAGGCCGGAGCGCGGGCCGCTGACGCCACTGTCGGGTGAGG GGCACGCGGCGTGGTCCCCAGAGCTAGGCCGGCGCGCGGGCCGCTGACGCCACTGTCGGGTGAGG T G LENG9 Ensembl:ENSG00000275183 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54463588..54463708 26863196 MeRIP-seq:(Medium) rs1328155535 Functional Loss SNV dbSNP153 33..33 33 - - - 70716 RMVar_ID_70716 Human_SNP_ID_669977608 m1A Human chr19 + 55010826 55010826 55010826 GAAGAATTGGGACCTAGCTCAGCCTGGGGAGGAGGGAGAGGTCAGACGGGTCTGTAGAAAAGGAA GAAGAATTGGGACCTAGCTCAGCCTGGGGAGGGGGGAGAGGTCAGACGGGTCTGTAGAAAAGGAA A G AC011476.3 Ensembl:ENSG00000267265 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55010775..55010864 26863196 MeRIP-seq:(Medium) rs1434980846 Functional Loss SNV dbSNP153 33..33 33 - - - 70717 RMVar_ID_70717 Human_SNP_ID_669987910 m1A Human chr19 - 55040422 55040422 55040422 GGCACTGGCCGGGCGCGGTGGCTCATGCCTGTATTCCCAGCACTTTGGGAGGCCAAATCACAAGG GGCACTGGCCGGGCGCGGTGGCTCATGCCTGTGTTCCCAGCACTTTGGGAGGCCAAATCACAAGG T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1392315946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248813,Human_RBP_ID_23180293 70718 RMVar_ID_70718 Human_SNP_ID_669989625 m1A Human chr19 - 55045213 55045213 55045213 CGTGGCGGAGGAACTGGCGGATGTTTCCGGAAAGTACTTCGATGGACTCAAACAGAAGGCCCCGG CGTGGCGGAGGAACTGGCGGATGTTTCCGGAAGGTACTTCGATGGACTCAAACAGAAGGCCCCGG T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55045162..55045247 26863196 MeRIP-seq:(Medium) rs1361040450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1570973,Human_RBP_ID_5099221 Human_Splice_Rec_2045534,Human_Splice_Rec_2045556,Human_Splice_Rec_2045568,Human_Splice_Rec_2045582,Human_Splice_Rec_2045596,Human_Splice_Rec_2045610 RMVar_hsa_circ_196252 70719 RMVar_ID_70719 Human_SNP_ID_670008231 m1A Human chr19 + 55095902 55095902 55095902 GGGACTCTTAGGGCTGGGGTGCGGCGGGGAGGAGACGCCATTGAGGGTTCTGGGTTCTGCAGGGG GGGACTCTTAGGGCTGGGGTGCGGCGGGGAGGGGACGCCATTGAGGGTTCTGGGTTCTGCAGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:55095503..55096228;chr19:55094986..55096175 26863196 MeRIP-seq:(Medium) rs778687136 Functional Loss SNV dbSNP153 33..33 33 - - - 70720 RMVar_ID_70720 Human_SNP_ID_670008592 m1A Human chr19 + 55096747 55096747 55096747 TCCTTCCCCGCGCAGTTCACCACCGTCTTCACACCTTCCCCGCAGTTCACCACCGTCTTCGCCCC TCCTTCCCCGCGCAGTTCACCACCGTCTTCACCCCTTCCCCGCAGTTCACCACCGTCTTCGCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55096673..55096783 26863196 MeRIP-seq:(Medium) rs942738046 Functional Loss SNV dbSNP153 33..33 33 - - - 70721 RMVar_ID_70721 Human_SNP_ID_670008593 m1A Human chr19 + 55096747 55096747 55096747 TCCTTCCCCGCGCAGTTCACCACCGTCTTCACACCTTCCCCGCAGTTCACCACCGTCTTCGCCCC TCCTTCCCCGCGCAGTTCACCACCGTCTTCACGCCTTCCCCGCAGTTCACCACCGTCTTCGCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55096673..55096783 26863196 MeRIP-seq:(Medium) rs942738046 Functional Loss SNV dbSNP153 33..33 33 - - - 70722 RMVar_ID_70722 Human_SNP_ID_670013395 m1A Human chr19 + 55112681 55112681 55112681 CCCTCCCTTGCCTCACCTGGCGATATCTAGGTAGCCACAGGAGGCGGCCACGTGCAGTGGCGTCC CCCTCCCTTGCCTCACCTGGCGATATCTAGGTTGCCACAGGAGGCGGCCACGTGCAGTGGCGTCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55112463..55112863 32194978 MeRIP-seq:(Medium) rs776034597 Functional Loss SNV dbSNP153 33..33 33 - - - 70723 RMVar_ID_70723 Human_SNP_ID_670013847 m1A Human chr19 + 55114043 55114043 55114043 CTCTCCCCATTCAGACCCAGGGGTCCAGGCCCAGCCCCGCCTCCCTAAGACCCAGAAGTCCAGGC CTCTCCCCATTCAGACCCAGGGGTCCAGGCCCCGCCCCGCCTCCCTAAGACCCAGAAGTCCAGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55114042..55114169 26863196 MeRIP-seq:(Medium) rs1435868313 Functional Loss SNV dbSNP153 33..33 33 - - - 70724 RMVar_ID_70724 Human_SNP_ID_670013852 m1A Human chr19 - 55114052 55114052 55114052 GGGCTGGGGGCCTGGACTTCTGGGTCTTAGGGAGGCGGGGCTGGGCCTGGACCCCTGGGTCTGAA GGGCTGGGGGCCTGGACTTCTGGGTCTTAGGGGGGCGGGGCTGGGCCTGGACCCCTGGGTCTGAA T C PPP1R12C Ensembl:ENSG00000125503 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55114045..55114253 26863196 MeRIP-seq:(Medium) rs1370189686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263364,Human_RBP_ID_3584009,Human_RBP_ID_5320581,Human_RBP_ID_5651143,Human_RBP_ID_8103220,Human_RBP_ID_8196871,Human_RBP_ID_8493659,Human_RBP_ID_9329194,Human_RBP_ID_9426438,Human_RBP_ID_18462017,Human_RBP_ID_22426379,Human_RBP_ID_22720191,Human_RBP_ID_26786043 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 70725 RMVar_ID_70725 Human_SNP_ID_670014745 m1A Human chr19 - 55117296 55117296 55117296 CGCCGCCGACCCTGGCCCCGGCGCCGAGCTCGACCCCGCCGCGCCGCCGCCCGCCCGCGCCGTGC CGCCGCCGACCCTGGCCCCGGCGCCGAGCTCGGCCCCGCCGCGCCGCCGCCCGCCCGCGCCGTGC T C PPP1R12C Ensembl:ENSG00000125503 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55117122..55117610 26863196 MeRIP-seq:(Medium) rs1030909322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239993,Human_RBP_ID_5469494,Human_RBP_ID_9329198,Human_RBP_ID_17132024,Human_RBP_ID_27471298 Human_Splice_Rec_2045953,Human_Splice_Rec_2046043 Human_miRNA_ID_2147470,Human_miRNA_ID_2988896,Human_miRNA_ID_3022599 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 70726 RMVar_ID_70726 Human_SNP_ID_670014785 m1A Human chr19 - 55117422 55117422 55117422 GGCGCGGGCGGGCGCCGAGCCTGGCCCCGGAGAGCGCCGCGCCCGCACCGTCCGCTTCGAGCGCG GGCGCGGGCGGGCGCCGAGCCTGGCCCCGGAGGGCGCCGCGCCCGCACCGTCCGCTTCGAGCGCG T C PPP1R12C Ensembl:ENSG00000125503 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55117201..55117600 26863196 MeRIP-seq:(Medium) rs761580796 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_526831,Human_RBP_ID_911989,Human_RBP_ID_5239467,Human_RBP_ID_17132025,Human_RBP_ID_24552880,Human_RBP_ID_26783878 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 70727 RMVar_ID_70727 Human_SNP_ID_670014801 m1A Human chr19 - 55117478 55117478 55117478 GGGGCGGCGGCGGCGGCTGCCCGGGAGCGGCGACGGGAGCAGCTGCGGCAGTGGGGGGCGCGGGC GGGGCGGCGGCGGCGGCTGCCCGGGAGCGGCGGCGGGAGCAGCTGCGGCAGTGGGGGGCGCGGGC T C PPP1R12C Ensembl:ENSG00000125503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55117177..55117625 26863196 MeRIP-seq:(Medium) rs1374647808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264108,Human_RBP_ID_3955588,Human_RBP_ID_4557694,Human_RBP_ID_5145423,Human_RBP_ID_5239467,Human_RBP_ID_5320583,Human_RBP_ID_9330264,Human_RBP_ID_17132026,Human_RBP_ID_18470669,Human_RBP_ID_18998776 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 70728 RMVar_ID_70728 Human_SNP_ID_670019458 m1A Human chr19 + 55132934 55132923 55132935 CGGGGCGGCATCCTCACTTCCAGCGGCCTCCAACGCGGCCCTTCCCTGCCCCCTTCCGGCTGTAG CGGGGCGGCATCCTCACTTCCA____________GCGGCCCTTCCCTGCCCCCTTCCGGCTGTAG AGCGGCCTCCAAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55132887..55133027 26863196 MeRIP-seq:(Medium) rs1384196096 Functional Loss DEL dbSNP153 23..34 33 - - - 70729 RMVar_ID_70729 Human_SNP_ID_670019459 m1A Human chr19 + 55132923 55132923 55132923 GTGCCACTGTCCGGGGCGGCATCCTCACTTCCAGCGGCCTCCAACGCGGCCCTTCCCTGCCCCCT GTGCCACTGTCCGGGGCGGCATCCTCACTTCCGGCGGCCTCCAACGCGGCCCTTCCCTGCCCCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55132876..55133016 26863196 MeRIP-seq:(Medium) rs1445057371 Functional Loss SNV dbSNP153 33..33 33 - - - 70730 RMVar_ID_70730 Human_SNP_ID_670019471 m1A Human chr19 - 55132948 55132948 55132948 ACCACCTCATTCTTCTACAGCCGGAAGGGGGCAGGGAAGGGCCGCGTTGGAGGCCGCTGGAAGTG ACCACCTCATTCTTCTACAGCCGGAAGGGGGCGGGGAAGGGCCGCGTTGGAGGCCGCTGGAAGTG T C TNNT1 Ensembl:ENSG00000105048 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55132851..55132975 32194978 MeRIP-seq:(Medium) rs1365147328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8561,Human_RBP_ID_5145424,Human_RBP_ID_9089646 Human_Splice_Rec_2046128,Human_Splice_Rec_2046154,Human_Splice_Rec_2046178,Human_Splice_Rec_2046204,Human_Splice_Rec_2046222,Human_Splice_Rec_2046236,Human_Splice_Rec_2046246,Human_Splice_Rec_2046266,Human_Splice_Rec_2046286,Human_Splice_Rec_2046304,Human_Splice_Rec_2046322,Human_Splice_Rec_2046330 70731 RMVar_ID_70731 Human_SNP_ID_670019480 m1A Human chr19 - 55132962 55132962 55132962 CCCTTTTTCCTGATACCACCTCATTCTTCTACAGCCGGAAGGGGGCAGGGAAGGGCCGCGTTGGA CCCTTTTTCCTGATACCACCTCATTCTTCTACGGCCGGAAGGGGGCAGGGAAGGGCCGCGTTGGA T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55132939..55133023 26863196 MeRIP-seq:(Medium) rs1555855228 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_293 70732 RMVar_ID_70732 Human_SNP_ID_670022279 m1A Human chr19 + 55141141 55141141 55141141 ATTATCTGCATCTCCCAAGATGCAAGGGATCCACATGGAGGGAGGAAGACCGGGGGGAACCCGGA ATTATCTGCATCTCCCAAGATGCAAGGGATCCGCATGGAGGGAGGAAGACCGGGGGGAACCCGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55141138..55141344 26863196 MeRIP-seq:(Medium) rs760374790 Functional Loss SNV dbSNP153 33..33 33 - - - 70733 RMVar_ID_70733 Human_SNP_ID_670022283 m1A Human chr19 - 55141144 55141144 55141144 GAGTCCGGGTTCCCCCCGGTCTTCCTCCCTCCATGTGGATCCCTTGCATCTTGGGAGATGCAGAT GAGTCCGGGTTCCCCCCGGTCTTCCTCCCTCCGTGTGGATCCCTTGCATCTTGGGAGATGCAGAT T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55141142..55141342 26863196 MeRIP-seq:(Medium) rs201147593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359246 RMVar_hsa_circ_31035,RMVar_hsa_circ_322550,RMVar_hsa_circ_277540,RMVar_hsa_circ_196272 70734 RMVar_ID_70734 Human_SNP_ID_670022284 m1A Human chr19 - 55141144 55141144 55141144 GAGTCCGGGTTCCCCCCGGTCTTCCTCCCTCCATGTGGATCCCTTGCATCTTGGGAGATGCAGAT GAGTCCGGGTTCCCCCCGGTCTTCCTCCCTCCCTGTGGATCCCTTGCATCTTGGGAGATGCAGAT T G TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55141142..55141342 26863196 MeRIP-seq:(Medium) rs201147593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359246 RMVar_hsa_circ_31035,RMVar_hsa_circ_322550,RMVar_hsa_circ_277540,RMVar_hsa_circ_196272 70735 RMVar_ID_70735 Human_SNP_ID_670022327 m1A Human chr19 + 55141204 55141204 55141204 GACTCTCGGCTCACAATGCGCTCCTTCAAGGCAACCAGCTCCTCTTCCTCCTTCTTCCGCTGCTC GACTCTCGGCTCACAATGCGCTCCTTCAAGGCGACCAGCTCCTCTTCCTCCTTCTTCCGCTGCTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55137101..55141957 32194978 MeRIP-seq:(Medium) rs1263854036 Functional Loss SNV dbSNP153 33..33 33 - - - 70736 RMVar_ID_70736 Human_SNP_ID_670022585 m1A Human chr19 + 55141905 55141905 55141905 TCCCCTTCTGGGATCTTTGGCGGGATCAAAGGAGGCACCACGGGGCGGCTGAGTGGACAGAAACA TCCCCTTCTGGGATCTTTGGCGGGATCAAAGGTGGCACCACGGGGCGGCTGAGTGGACAGAAACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55141813..55141968 26863196 MeRIP-seq:(Medium) rs141999523 Functional Loss SNV dbSNP153 33..33 33 - - - 70737 RMVar_ID_70737 Human_SNP_ID_670023722 m1A Human chr19 + 55145527 55145527 55145527 ATATTTAGGAAGATGTATGACTGGGGCCCCCCACCCTGTAGGATCTCACCTTGGTTTGGGGCGTT ATATTTAGGAAGATGTATGACTGGGGCCCCCCCCCCTGTAGGATCTCACCTTGGTTTGGGGCGTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55145526..55145575 26863196 MeRIP-seq:(Medium) rs201135309 Functional Loss SNV dbSNP153 33..33 33 - - - 70738 RMVar_ID_70738 Human_SNP_ID_670051859 m1A Human chr19 - 55229185 55229185 55229185 TGGTGGGGTTGAGCAGAATGAGGAAAGGTTTCATGGAGCAGGGAGGGAGACGGCTAGGGCAGCAA TGGTGGGGTTGAGCAGAATGAGGAAAGGTTTCGTGGAGCAGGGAGGGAGACGGCTAGGGCAGCAA T C AC010327.6 Ensembl:ENSG00000276570 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55229135..55229273 26863196 MeRIP-seq:(Medium) rs758265581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263371,Human_RBP_ID_824351,Human_RBP_ID_908120,Human_RBP_ID_3955598,Human_RBP_ID_4546895,Human_RBP_ID_6783743,Human_RBP_ID_8100821,Human_RBP_ID_8199986,Human_RBP_ID_22663199,Human_RBP_ID_26338291,Human_RBP_ID_26472886 70739 RMVar_ID_70739 Human_SNP_ID_670051863 m1A Human chr19 - 55229192 55229192 55229192 GAGGGCTTGGTGGGGTTGAGCAGAATGAGGAAAGGTTTCATGGAGCAGGGAGGGAGACGGCTAGG GAGGGCTTGGTGGGGTTGAGCAGAATGAGGAAGGGTTTCATGGAGCAGGGAGGGAGACGGCTAGG T C AC010327.6 Ensembl:ENSG00000276570 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55229141..55229221 26863196 MeRIP-seq:(Medium) rs889569725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263371,Human_RBP_ID_908120,Human_RBP_ID_3955598,Human_RBP_ID_6783743,Human_RBP_ID_8100821,Human_RBP_ID_8199986,Human_RBP_ID_22663199,Human_RBP_ID_23807049,Human_RBP_ID_26338291,Human_RBP_ID_26472886 Human_miRNA_ID_3208921 70740 RMVar_ID_70740 Human_SNP_ID_670052181 m1A Human chr19 + 55230176 55230176 55230176 ACCCCTAACACCAGCTCCCGCTGGGACGGAACAGGGAAGGCTGTGCTTTGGAGCCGCCAGCCCAG ACCCCTAACACCAGCTCCCGCTGGGACGGAACGGGGAAGGCTGTGCTTTGGAGCCGCCAGCCCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55230081..55230180 26863410 MeRIP-seq:(Medium) rs528708153 Functional Loss SNV dbSNP153 33..33 33 - - - 70741 RMVar_ID_70741 Human_SNP_ID_670052294 m1A Human chr19 - 55230502 55230502 55230502 CAGATAGCTGCCTGGTGCGGCAGCGGCGGCCAAATCTTCCGTCCTCCCGTGGATCTCCCGGGGTG CAGATAGCTGCCTGGTGCGGCAGCGGCGGCCACATCTTCCGTCCTCCCGTGGATCTCCCGGGGTG T G PPP6R1 Ensembl:ENSG00000105063 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55230401..55230505 26863410 MeRIP-seq:(Medium) rs766523064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8564,Human_RBP_ID_22812225 Human_Splice_Rec_2046950,Human_Splice_Rec_2046962,Human_Splice_Rec_2047006 Human_miRNA_ID_2135211 RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_114177,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_196289,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_196284 70742 RMVar_ID_70742 Human_SNP_ID_670052553 m1A Human chr19 + 55230868 55230868 55230868 CTGGTGGGCCCCGGAGGCTGGGACAGAGGTAGAGGGGTCTCTGGTTGCACTGTGGGTGAGAGGCA CTGGTGGGCCCCGGAGGCTGGGACAGAGGTAGGGGGGTCTCTGGTTGCACTGTGGGTGAGAGGCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55230743..55230900 26863196 MeRIP-seq:(Medium) rs1401350601 Functional Loss SNV dbSNP153 33..33 33 - - - 70743 RMVar_ID_70743 Human_SNP_ID_670052923 m1A Human chr19 - 55231616 55231616 55231616 CCTCAGCACCTCAGGAAGCCACAGAAGGCAGCAAAGTCACGGAGCCCTCAGGTGAGCCCCGCTTT CCTCAGCACCTCAGGAAGCCACAGAAGGCAGCGAAGTCACGGAGCCCTCAGGTGAGCCCCGCTTT T C PPP6R1 Ensembl:ENSG00000105063 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55231601..55231650 26863196 MeRIP-seq:(Medium) rs1258119234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387511 Human_Splice_Rec_2046942,Human_Splice_Rec_2046943,Human_Splice_Rec_2046954,Human_Splice_Rec_2046955,Human_Splice_Rec_2046998,Human_Splice_Rec_2046999 Human_miRNA_ID_2377013,Human_miRNA_ID_2465272,Human_miRNA_ID_3032659 RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_57099,RMVar_hsa_circ_117601,RMVar_hsa_circ_196290 70744 RMVar_ID_70744 Human_SNP_ID_670053254 m1A Human chr19 - 55232196 55232196 55232196 GGTGGTTTCTGGGGCAGGAGTGGAGGCAGCACAGACAGTGAGGACGAAGAAGAGGAGGACGAGGA GGTGGTTTCTGGGGCAGGAGTGGAGGCAGCACTGACAGTGAGGACGAAGAAGAGGAGGACGAGGA T A PPP6R1 Ensembl:ENSG00000105063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55232076..55232240 26863196 MeRIP-seq:(Medium) rs764826884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53094,Human_RBP_ID_2570269,Human_RBP_ID_3955601,Human_RBP_ID_9347041,Human_RBP_ID_18998791,Human_RBP_ID_26472894 Human_Splice_Rec_2046938,Human_Splice_Rec_2046994 RMVar_hsa_circ_6662,RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_57099 70745 RMVar_ID_70745 Human_SNP_ID_670053255 m1A Human chr19 - 55232196 55232196 55232196 GGTGGTTTCTGGGGCAGGAGTGGAGGCAGCACAGACAGTGAGGACGAAGAAGAGGAGGACGAGGA GGTGGTTTCTGGGGCAGGAGTGGAGGCAGCACGGACAGTGAGGACGAAGAAGAGGAGGACGAGGA T C PPP6R1 Ensembl:ENSG00000105063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55232076..55232240 26863196 MeRIP-seq:(Medium) rs764826884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53094,Human_RBP_ID_2570269,Human_RBP_ID_3955601,Human_RBP_ID_9347041,Human_RBP_ID_18998791,Human_RBP_ID_26472894 Human_Splice_Rec_2046938,Human_Splice_Rec_2046994 RMVar_hsa_circ_6662,RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_57099 70746 RMVar_ID_70746 Human_SNP_ID_670054647 m1A Human chr19 - 55236628 55236628 55236628 CCAGCCACCTGGTGTCCGGTGAGTCCCCCTCCAGTTTCCCTTCTCCAAGCTTCCACCACACGGCA CCAGCCACCTGGTGTCCGGTGAGTCCCCCTCCGGTTTCCCTTCTCCAAGCTTCCACCACACGGCA T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55236626..55236750 26863196 MeRIP-seq:(Medium) rs951263381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090924 RMVar_hsa_circ_6662,RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_57099 70747 RMVar_ID_70747 Human_SNP_ID_670055747 m1A Human chr19 - 55239911 55239911 55239911 GCCTCACGTCTTCACCCCTCTCACCTAAGCAGAGCTGCCCAGCGAGCAGCAGGAGCAGTGGGAAG GCCTCACGTCTTCACCCCTCTCACCTAAGCAGGGCTGCCCAGCGAGCAGCAGGAGCAGTGGGAAG T C PPP6R1 Ensembl:ENSG00000105063 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55239903..55239987 26863196 MeRIP-seq:(Medium) rs371276806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2046928,Human_Splice_Rec_2046929,Human_Splice_Rec_2046984,Human_Splice_Rec_2046985 Human_miRNA_ID_3056107 RMVar_hsa_circ_91556,RMVar_hsa_circ_108535,RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_196287,RMVar_hsa_circ_80831,RMVar_hsa_circ_196288,RMVar_hsa_circ_196286,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_57099,RMVar_hsa_circ_85532,RMVar_hsa_circ_99208,RMVar_hsa_circ_196292,RMVar_hsa_circ_342371,RMVar_hsa_circ_374135,RMVar_hsa_circ_67994,RMVar_hsa_circ_102612,RMVar_hsa_circ_93017,RMVar_hsa_circ_196294,RMVar_hsa_circ_196295,RMVar_hsa_circ_117380,RMVar_hsa_circ_369978,RMVar_hsa_circ_196296,RMVar_hsa_circ_196297,RMVar_hsa_circ_196298,RMVar_hsa_circ_114159,RMVar_hsa_circ_196299,RMVar_hsa_circ_196300 70748 RMVar_ID_70748 Human_SNP_ID_670058565 m1A Human chr19 + 55247090 55247090 55247090 GCGTGTCCAGGTGCGAGCTTGTGTGCAGGTCAAACTTCCAAAACATGGCGCCCTGCAGGCATAGA GCGTGTCCAGGTGCGAGCTTGTGTGCAGGTCAGACTTCCAAAACATGGCGCCCTGCAGGCATAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55246988..55247154 26863196 MeRIP-seq:(Medium) rs996587233 Functional Loss SNV dbSNP153 33..33 33 - - - 70749 RMVar_ID_70749 Human_SNP_ID_670061634 m1A Human chr19 - 55257545 55257545 55257545 GGGGGGAAGGAGCAGCACGTGCAGATATGTCAAGGAAGGAAGGTCGGAGTCCTGAGTGCAGATGT GGGGGGAAGGAGCAGCACGTGCAGATATGTCAGGGAAGGAAGGTCGGAGTCCTGAGTGCAGATGT T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55257543..55257624 26863196 MeRIP-seq:(Medium) rs1386587603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93017,RMVar_hsa_circ_196296,RMVar_hsa_circ_81690,RMVar_hsa_circ_196305 70750 RMVar_ID_70750 Human_SNP_ID_670062058 m1A Human chr19 - 55258532 55258532 55258532 GCGAGTCCCCGACGCCGCCCCCGCCCCCACTCACCGGGCCCCGCAGCAGGGGCCGGAGCCGCCGG GCGAGTCCCCGACGCCGCCCCCGCCCCCACTCCCCGGGCCCCGCAGCAGGGGCCGGAGCCGCCGG T G PPP6R1 Ensembl:ENSG00000105063 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:55258448..55258553 26863410 MeRIP-seq:(Medium) rs1437504481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4547038,Human_RBP_ID_5321917 Human_Splice_Rec_2046905 Human_miRNA_ID_2513289,Human_miRNA_ID_3056108,Human_miRNA_ID_3066430 RMVar_hsa_circ_93017,RMVar_hsa_circ_196296,RMVar_hsa_circ_81690,RMVar_hsa_circ_196305 70751 RMVar_ID_70751 Human_SNP_ID_670063367 m1A Human chr19 + 55262454 55262454 55262454 GAGGTGGGGTCCAAGGAGCTGGTGCCTTTCTCAGCGCCCCTTCCAGGGACTGCACAGAGACGGGC GAGGTGGGGTCCAAGGAGCTGGTGCCTTTCTCCGCGCCCCTTCCAGGGACTGCACAGAGACGGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55262405..55262493 26863196 MeRIP-seq:(Medium) rs1469887414 Functional Loss SNV dbSNP153 33..33 33 - - - 70752 RMVar_ID_70752 Human_SNP_ID_670064026 m1A Human chr19 - 55265046 55265046 55265046 GATGGGGTTCGAGGAGGATCGTGTGCCGGGGGAGGGGACAGCGGCTCCAGAAGGACCAGGTGAGT GATGGGGTTCGAGGAGGATCGTGTGCCGGGGGTGGGGACAGCGGCTCCAGAAGGACCAGGTGAGT T A HSPBP1 Ensembl:ENSG00000133265 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55265043..55265161 26863196 MeRIP-seq:(Medium) rs1426899492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112241,RMVar_hsa_circ_196311,RMVar_hsa_circ_110233,RMVar_hsa_circ_196310 70753 RMVar_ID_70753 Human_SNP_ID_670067554 m1A Human chr19 - 55277600 55277600 55277600 TTCCCCCGCCAGGACGTTCTGCCCCTCTGTACATGTCCTGCTGCCTCTCAGCTCTTGCCCCTACT TTCCCCCGCCAGGACGTTCTGCCCCTCTGTACGTGTCCTGCTGCCTCTCAGCTCTTGCCCCTACT T C HSPBP1 Ensembl:ENSG00000133265 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55277598..55277759 26863196 MeRIP-seq:(Medium) rs758335549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57137,RMVar_hsa_circ_196311,RMVar_hsa_circ_110233 70754 RMVar_ID_70754 Human_SNP_ID_670068238 m1A Human chr19 + 55279633 55279633 55279633 TCTGACATGGGCCGTTTGTGAAGAAGGGAAGAATGTGTTAGAGGGAGAAGGTGGTCACCGCTGAA TCTGACATGGGCCGTTTGTGAAGAAGGGAAGATTGTGTTAGAGGGAGAAGGTGGTCACCGCTGAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55279471..55279757 26863196 MeRIP-seq:(Medium) rs1386368534 Functional Loss SNV dbSNP153 33..33 33 - - - 70755 RMVar_ID_70755 Human_SNP_ID_670068351 m1A Human chr19 - 55280000 55280000 55280000 GAGATCCGCCTTATTCCGGCGCCCCTCTTCGGAGAGGAGGGAGAAGACTTGTTGCTAAGGAGACC GAGATCCGCCTTATTCCGGCGCCCCTCTTCGGCGAGGAGGGAGAAGACTTGTTGCTAAGGAGACC T G HSPBP1 Ensembl:ENSG00000133265 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55279998..55280106 32194978 MeRIP-seq:(Medium) rs975124210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558770 Human_Splice_Rec_2047087 70756 RMVar_ID_70756 Human_SNP_ID_670068485 m1A Human chr19 - 55280337 55280336 55280337 GGCGGGACTCGCTGAGGTGCGAAAACTGGGCCAGGGGCAGGGCTTTGACCAGCTACTTGAGCGTG GGCGGGACTCGCTGAGGTGCGAAAACTGGGCC_GGGGCAGGGCTTTGACCAGCTACTTGAGCGTG CT C HSPBP1 Ensembl:ENSG00000133265 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55279959..55280358 26863196 MeRIP-seq:(Medium) rs879295850 Functional Loss DEL dbSNP153 33..33 33 - - - 70757 RMVar_ID_70757 Human_SNP_ID_670068486 m1A Human chr19 - 55280337 55280337 55280337 GGCGGGACTCGCTGAGGTGCGAAAACTGGGCCAGGGGCAGGGCTTTGACCAGCTACTTGAGCGTG GGCGGGACTCGCTGAGGTGCGAAAACTGGGCCGGGGGCAGGGCTTTGACCAGCTACTTGAGCGTG T C HSPBP1 Ensembl:ENSG00000133265 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55279959..55280358 26863196 MeRIP-seq:(Medium) rs1256710593 Functional Loss SNV dbSNP153 33..33 33 - - - 70758 RMVar_ID_70758 Human_SNP_ID_670075182 m1A Human chr19 - 55303748 55303748 55303748 GGGAGCCACCACCCCCGGCATCGGTGATGCTCAGGACTTCCATGGACTTCCGCTCTGGTCGCCGC GGGAGCCACCACCCCCGGCATCGGTGATGCTCGGGACTTCCATGGACTTCCGCTCTGGTCGCCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55303697..55305501 32194978 MeRIP-seq:(Medium) rs1164458618 Functional Loss SNV dbSNP153 33..33 33 - - - 70759 RMVar_ID_70759 Human_SNP_ID_670076133 m1A Human chr19 + 55306444 55306444 55306444 GTGGTGGCATCTACTCCGTCACCTTCACTCTCATCTCGGGTGAGTCTCTTGGCTAGGCTGCCTGC GTGGTGGCATCTACTCCGTCACCTTCACTCTCGTCTCGGGTGAGTCTCTTGGCTAGGCTGCCTGC A G BRSK1 Ensembl:ENSG00000160469 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55306264..55312084 32194978 MeRIP-seq:(Medium) rs1475493580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17930940 Human_Splice_Rec_2047141,Human_Splice_Rec_2047189,Human_Splice_Rec_2047235 RMVar_hsa_circ_7753 70760 RMVar_ID_70760 Human_SNP_ID_670086450 m1A Human chr19 + 55339944 55339944 55339944 GTTGGCGGCGGCGGCGCGGGCGCCTGAGGAGGAGGAGGAGAAGCGGGTGAGGGGCGGCGCGGGGC GTTGGCGGCGGCGGCGCGGGCGCCTGAGGAGGCGGAGGAGAAGCGGGTGAGGGGCGGCGCGGGGC A C KMT5C Ensembl:ENSG00000133247 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55339895..55340017 26863196 MeRIP-seq:(Medium) rs1008272020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2047325,Human_Splice_Rec_2047331,Human_Splice_Rec_2047335,Human_Splice_Rec_2047351,Human_Splice_Rec_2047355 RMVar_hsa_circ_196319,RMVar_hsa_circ_96083,RMVar_hsa_circ_99851,RMVar_hsa_circ_196320 70761 RMVar_ID_70761 Human_SNP_ID_670086497 m1A Human chr19 - 55340073 55340073 55340073 GAGGGGCCGGGAGACGTGGGCGCCTGGACACGAGGAGGGGCCGGGCGGGGTGGGGGGCAGTCGGG GAGGGGCCGGGAGACGTGGGCGCCTGGACACGGGGAGGGGCCGGGCGGGGTGGGGGGCAGTCGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55340071..55340372 26863196 MeRIP-seq:(Medium) rs1169287379 Functional Loss SNV dbSNP153 33..33 33 - - - 70762 RMVar_ID_70762 Human_SNP_ID_670086521 m1A Human chr19 - 55340120 55340120 55340120 GGAAGCACAGGAAGGAGGCTGCAGTGCCGCGGAGCCCGAGGCCCGGCGAGGGGCCGGGAGACGTG GGAAGCACAGGAAGGAGGCTGCAGTGCCGCGGCGCCCGAGGCCCGGCGAGGGGCCGGGAGACGTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55340095..55340293 26863196 MeRIP-seq:(Medium) rs958462797 Functional Loss SNV dbSNP153 33..33 33 - - - 70763 RMVar_ID_70763 Human_SNP_ID_670087033 m1A Human chr19 + 55341845 55341845 55341845 CAGCGTCCCCCATGGCTTCTGAGTAGCGTGGGAGTGGAGTCAGCACCAAGCCAGGCTCCCCGCGC CAGCGTCCCCCATGGCTTCTGAGTAGCGTGGGCGTGGAGTCAGCACCAAGCCAGGCTCCCCGCGC A C KMT5C Ensembl:ENSG00000133247 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55341773..55342076 26863196 MeRIP-seq:(Medium) rs1002562075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571033,Human_RBP_ID_5191818,Human_RBP_ID_9330272,Human_RBP_ID_18998814,Human_RBP_ID_26336837 Human_Splice_Rec_2047326,Human_Splice_Rec_2047332,Human_Splice_Rec_2047336,Human_Splice_Rec_2047352,Human_Splice_Rec_2047356 Human_miRNA_ID_2454627,Human_miRNA_ID_2868861,Human_miRNA_ID_2949813 RMVar_hsa_circ_196319,RMVar_hsa_circ_96083,RMVar_hsa_circ_99851,RMVar_hsa_circ_196320,RMVar_hsa_circ_196321,RMVar_hsa_circ_292301,RMVar_hsa_circ_369441,RMVar_hsa_circ_196322 70764 RMVar_ID_70764 Human_SNP_ID_670088025 m1A Human chr19 - 55344620 55344620 55344620 TTGTTCCCTGCAAGGCCGGGGGCTCCCACCACAGGGCCCTGCCTCCCTGCCACACTCCCTGCCCA TTGTTCCCTGCAAGGCCGGGGGCTCCCACCACGGGGCCCTGCCTCCCTGCCACACTCCCTGCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55344569..55344762 26863196 MeRIP-seq:(Medium) rs774899615 Functional Loss SNV dbSNP153 33..33 33 - - - 70765 RMVar_ID_70765 Human_SNP_ID_670088059 m1A Human chr19 + 55344678 55344678 55344678 GGAACAACGCAGGCAGCTGTGGTGGCAGGAGCAGGGAGGCCAGAGAGCCCCAGGGGCCAGGACTC GGAACAACGCAGGCAGCTGTGGTGGCAGGAGCGGGGAGGCCAGAGAGCCCCAGGGGCCAGGACTC A G KMT5C Ensembl:ENSG00000133247 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55344630..55344794 26863196 MeRIP-seq:(Medium) rs754994852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825398,Human_RBP_ID_5321923,Human_RBP_ID_22665997 Human_Splice_Rec_2047354 RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_292301,RMVar_hsa_circ_196322 70766 RMVar_ID_70766 Human_SNP_ID_670088073 m1A Human chr19 + 55344704 55344704 55344704 AGGAGCAGGGAGGCCAGAGAGCCCCAGGGGCCAGGACTCAGGATGCTGTCCAGACATGCCCAGGA AGGAGCAGGGAGGCCAGAGAGCCCCAGGGGCCGGGACTCAGGATGCTGTCCAGACATGCCCAGGA A G KMT5C Ensembl:ENSG00000133247 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55344653..55344765 26863196 MeRIP-seq:(Medium) rs1219338101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5321923,Human_RBP_ID_22665997 Human_Splice_Rec_2047354 RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_292301,RMVar_hsa_circ_196322 70767 RMVar_ID_70767 Human_SNP_ID_670088983 m1A Human chr19 + 55347034 55347034 55347034 CACCTCACCCCTCTGGCTCCAGTGGCTGCCTCAGCCCCAGCCCCGAGTGCGGCCCCGGAAGCGCC CACCTCACCCCTCTGGCTCCAGTGGCTGCCTCGGCCCCAGCCCCGAGTGCGGCCCCGGAAGCGCC A G KMT5C Ensembl:ENSG00000133247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55346562..55347482 26863196 MeRIP-seq:(Medium) rs1324240717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2047350,Human_Splice_Rec_2047368,Human_Splice_Rec_2047384,Human_Splice_Rec_2047420 Human_miRNA_ID_1358605 RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_93230,RMVar_hsa_circ_196324 70768 RMVar_ID_70768 Human_SNP_ID_670099417 m1A Human chr19 - 55378201 55378201 55378201 TCTGTATTGAGCAGTCCCCCGGGGACTCCCCTAATCCTCCTCTTCCTCGCCCTCTGTCTCCTCAC TCTGTATTGAGCAGTCCCCCGGGGACTCCCCTGATCCTCCTCTTCCTCGCCCTCTGTCTCCTCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55378190..55378280 26863196 MeRIP-seq:(Medium) rs1050628347 Functional Loss SNV dbSNP153 33..33 33 - - - 70769 RMVar_ID_70769 Human_SNP_ID_670101024 m1A Human chr19 + 55384022 55384022 55384022 GTACCAGAGGATCCAGCCCAGCAGGCTCAGGAACACCAGCAGCGCGCCCGAGTAGATGAGCAGGT GTACCAGAGGATCCAGCCCAGCAGGCTCAGGAGCACCAGCAGCGCGCCCGAGTAGATGAGCAGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55383985..55384248 26863196 MeRIP-seq:(Medium) rs1192501905 Functional Loss SNV dbSNP153 33..33 33 - - - 70770 RMVar_ID_70770 Human_SNP_ID_670101640 m1A Human chr19 - 55385955 55385955 55385955 CGCGAGGAAGACGAACGCTCACCTCCCTTCGCAGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG CGCGAGGAAGACGAACGCTCACCTCCCTTCGCTGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs562997171 Functional Loss SNV dbSNP153 33..33 33 - - - 70771 RMVar_ID_70771 Human_SNP_ID_670101641 m1A Human chr19 - 55385955 55385955 55385955 CGCGAGGAAGACGAACGCTCACCTCCCTTCGCAGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG CGCGAGGAAGACGAACGCTCACCTCCCTTCGCGGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs562997171 Functional Loss SNV dbSNP153 33..33 33 - - - 70772 RMVar_ID_70772 Human_SNP_ID_670101650 m1A Human chr19 + 55385960 55385960 55385960 CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGACGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC A C RPL28 Ensembl:ENSG00000108107 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs756872430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239911,Human_RBP_ID_771031,Human_RBP_ID_825365,Human_RBP_ID_913155,Human_RBP_ID_4558772,Human_RBP_ID_5145433,Human_RBP_ID_17655390,Human_RBP_ID_22449030,Human_RBP_ID_22533492 Human_Splice_Rec_2047553,Human_Splice_Rec_2047557,Human_Splice_Rec_2047563,Human_Splice_Rec_2047571,Human_Splice_Rec_2047579,Human_Splice_Rec_2047585,Human_Splice_Rec_2047593 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326 70773 RMVar_ID_70773 Human_SNP_ID_670101651 m1A Human chr19 + 55385960 55385960 55385960 CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGAGGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC A G RPL28 Ensembl:ENSG00000108107 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs756872430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239911,Human_RBP_ID_771031,Human_RBP_ID_825365,Human_RBP_ID_913155,Human_RBP_ID_4558772,Human_RBP_ID_5145433,Human_RBP_ID_17655390,Human_RBP_ID_22449030,Human_RBP_ID_22533492 Human_Splice_Rec_2047553,Human_Splice_Rec_2047557,Human_Splice_Rec_2047563,Human_Splice_Rec_2047571,Human_Splice_Rec_2047579,Human_Splice_Rec_2047585,Human_Splice_Rec_2047593 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326 70774 RMVar_ID_70774 Human_SNP_ID_670101652 m1A Human chr19 + 55385960 55385960 55385960 CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC CTTCCTCTTTCCGTCTCAGGTCGCCGCTGCGATGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTC A T RPL28 Ensembl:ENSG00000108107 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs756872430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239911,Human_RBP_ID_771031,Human_RBP_ID_825365,Human_RBP_ID_913155,Human_RBP_ID_4558772,Human_RBP_ID_5145433,Human_RBP_ID_17655390,Human_RBP_ID_22449030,Human_RBP_ID_22533492 Human_Splice_Rec_2047553,Human_Splice_Rec_2047557,Human_Splice_Rec_2047563,Human_Splice_Rec_2047571,Human_Splice_Rec_2047579,Human_Splice_Rec_2047585,Human_Splice_Rec_2047593 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326 70775 RMVar_ID_70775 Human_SNP_ID_670101658 m1A Human chr19 + 55385964 55385964 55385964 CTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTCGCCA CTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGGGGTGAGCGTTCGTCTTCCTCGCGTGGTCGCCA A G RPL28 Ensembl:ENSG00000108107 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55385926..55386043;chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs936541532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239911,Human_RBP_ID_771031,Human_RBP_ID_825365,Human_RBP_ID_913155,Human_RBP_ID_4558773,Human_RBP_ID_5145433,Human_RBP_ID_17655390,Human_RBP_ID_22449030,Human_RBP_ID_22533492 Human_Splice_Rec_2047553,Human_Splice_Rec_2047557,Human_Splice_Rec_2047563,Human_Splice_Rec_2047571,Human_Splice_Rec_2047579,Human_Splice_Rec_2047585,Human_Splice_Rec_2047593 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326 70776 RMVar_ID_70776 Human_SNP_ID_670101659 m1A Human chr19 + 55385964 55385964 55385964 CTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGAGGTGAGCGTTCGTCTTCCTCGCGTGGTCGCCA CTCTTTCCGTCTCAGGTCGCCGCTGCGAAGGGTGGTGAGCGTTCGTCTTCCTCGCGTGGTCGCCA A T RPL28 Ensembl:ENSG00000108107 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55385926..55386043;chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs936541532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239911,Human_RBP_ID_771031,Human_RBP_ID_825365,Human_RBP_ID_913155,Human_RBP_ID_4558773,Human_RBP_ID_5145433,Human_RBP_ID_17655390,Human_RBP_ID_22449030,Human_RBP_ID_22533492 Human_Splice_Rec_2047553,Human_Splice_Rec_2047557,Human_Splice_Rec_2047563,Human_Splice_Rec_2047571,Human_Splice_Rec_2047579,Human_Splice_Rec_2047585,Human_Splice_Rec_2047593 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326 70777 RMVar_ID_70777 Human_SNP_ID_670101841 m1A Human chr19 + 55386413 55386413 55386413 GGTCGTGCGGAACTGCTCCAGTTTCCTGATCAAGAGGAATAAGCAGACCTACAGCACTGTAAGTG GGTCGTGCGGAACTGCTCCAGTTTCCTGATCAGGAGGAATAAGCAGACCTACAGCACTGTAAGTG A G RPL28 Ensembl:ENSG00000108107 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:55386351..55386450 32194978 MeRIP-seq:(Medium) rs1412851680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526941,Human_RBP_ID_1571049,Human_RBP_ID_1891758,Human_RBP_ID_9089673,Human_RBP_ID_23807256 Human_Splice_Rec_2047554,Human_Splice_Rec_2047555,Human_Splice_Rec_2047558,Human_Splice_Rec_2047559,Human_Splice_Rec_2047564,Human_Splice_Rec_2047565,Human_Splice_Rec_2047572,Human_Splice_Rec_2047573,Human_Splice_Rec_2047580,Human_Splice_Rec_2047581,Human_Splice_Rec_2047586,Human_Splice_Rec_2047587,Human_Splice_Rec_2047594,Human_Splice_Rec_2047595,Human_Splice_Rec_2047599,Human_Splice_Rec_2047605,Human_Splice_Rec_2047611,Human_Splice_Rec_2047613 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326,RMVar_hsa_circ_344000 70778 RMVar_ID_70778 Human_SNP_ID_670101856 m1A Human chr19 + 55386436 55386436 55386436 TCCTGATCAAGAGGAATAAGCAGACCTACAGCACTGTAAGTGGGGCCCGGATGCGTGGCTCCTGC TCCTGATCAAGAGGAATAAGCAGACCTACAGCTCTGTAAGTGGGGCCCGGATGCGTGGCTCCTGC A T RPL28 Ensembl:ENSG00000108107 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55386326..55386725 26863410 MeRIP-seq:(Medium) rs1418540879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571050,Human_RBP_ID_19094293,Human_RBP_ID_23807256 Human_Splice_Rec_2047554,Human_Splice_Rec_2047555,Human_Splice_Rec_2047558,Human_Splice_Rec_2047559,Human_Splice_Rec_2047564,Human_Splice_Rec_2047565,Human_Splice_Rec_2047572,Human_Splice_Rec_2047573,Human_Splice_Rec_2047580,Human_Splice_Rec_2047581,Human_Splice_Rec_2047586,Human_Splice_Rec_2047587,Human_Splice_Rec_2047594,Human_Splice_Rec_2047595,Human_Splice_Rec_2047599,Human_Splice_Rec_2047605,Human_Splice_Rec_2047611,Human_Splice_Rec_2047613 RMVar_hsa_circ_98465,RMVar_hsa_circ_120940,RMVar_hsa_circ_196327,RMVar_hsa_circ_91071,RMVar_hsa_circ_196328,RMVar_hsa_circ_196326,RMVar_hsa_circ_344000 70779 RMVar_ID_70779 Human_SNP_ID_670101918 m1A Human chr19 - 55386553 55386553 55386553 TCAAGTTATTGGGCTCCTGGGAAGGAGGCGGCACAAGGCATCGTGAATAAGGGACCCGGAGACAT TCAAGTTATTGGGCTCCTGGGAAGGAGGCGGCTCAAGGCATCGTGAATAAGGGACCCGGAGACAT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr19:55386551..55386575;chr19:55386551..55386600 26863196,32194978 MeRIP-seq:(Medium) rs1444403542 Functional Loss SNV dbSNP153 33..33 33 - - - 70780 RMVar_ID_70780 Human_SNP_ID_670101919 m1A Human chr19 - 55386553 55386553 55386553 TCAAGTTATTGGGCTCCTGGGAAGGAGGCGGCACAAGGCATCGTGAATAAGGGACCCGGAGACAT TCAAGTTATTGGGCTCCTGGGAAGGAGGCGGCCCAAGGCATCGTGAATAAGGGACCCGGAGACAT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr19:55386551..55386575;chr19:55386551..55386600 26863196,32194978 MeRIP-seq:(Medium) rs1444403542 Functional Loss SNV dbSNP153 33..33 33 - - - 70781 RMVar_ID_70781 Human_SNP_ID_670101990 m1A Human chr19 - 55386695 55386695 55386695 GGCCGCTCTCTGGCCCAAACCAGACAAAACTCACCGGATCTCCGCTTAATGACCACCACGACACC GGCCGCTCTCTGGCCCAAACCAGACAAAACTCTCCGGATCTCCGCTTAATGACCACCACGACACC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr19:55386676..55386700;chr19:55386541..55386745 26863196 MeRIP-seq:(Medium) rs113906929 Functional Loss SNV dbSNP153 33..33 33 - - - 70782 RMVar_ID_70782 Human_SNP_ID_670101991 m1A Human chr19 - 55386695 55386695 55386695 GGCCGCTCTCTGGCCCAAACCAGACAAAACTCACCGGATCTCCGCTTAATGACCACCACGACACC GGCCGCTCTCTGGCCCAAACCAGACAAAACTCGCCGGATCTCCGCTTAATGACCACCACGACACC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr19:55386676..55386700;chr19:55386541..55386745 26863196 MeRIP-seq:(Medium) rs113906929 Functional Loss SNV dbSNP153 33..33 33 - - - 70783 RMVar_ID_70783 Human_SNP_ID_670102509 m1A Human chr19 - 55388014 55388014 55388014 TGCGCAGGTCGGGGCGGTACTTGTTCTTGCGGATCATGTGTCTGATGCTGCTGAGCGTGGCGCGA TGCGCAGGTCGGGGCGGTACTTGTTCTTGCGGGTCATGTGTCTGATGCTGCTGAGCGTGGCGCGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:55387951..55388350;chr19:55387951..55388280;chr19:55387926..55388375 26863196 MeRIP-seq:(Medium) rs77906615 Functional Loss SNV dbSNP153 33..33 33 - - - 70784 RMVar_ID_70784 Human_SNP_ID_670102519 m1A Human chr19 + 55388026 55388026 55388026 CAGCAGCATCAGACACATGATCCGCAAGAACAAGTACCGCCCCGACCTGCGCATGGTGAGCTGGG CAGCAGCATCAGACACATGATCCGCAAGAACAGGTACCGCCCCGACCTGCGCATGGTGAGCTGGG A G RPL28 Ensembl:ENSG00000108107 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:55387976..55388025 26863196 MeRIP-seq:(Medium) rs1365341987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571066,Human_RBP_ID_1891763,Human_RBP_ID_13509598 Human_Splice_Rec_2047568,Human_Splice_Rec_2047569,Human_Splice_Rec_2047576,Human_Splice_Rec_2047577,Human_Splice_Rec_2047584,Human_Splice_Rec_2047590,Human_Splice_Rec_2047591,Human_Splice_Rec_2047597,Human_Splice_Rec_2047602,Human_Splice_Rec_2047603,Human_Splice_Rec_2047608,Human_Splice_Rec_2047609 Human_miRNA_ID_2387495,Human_miRNA_ID_2387496,Human_miRNA_ID_2388969,Human_miRNA_ID_2388970,Human_miRNA_ID_2400117,Human_miRNA_ID_2400118,Human_miRNA_ID_3031180,Human_miRNA_ID_3031181 RMVar_hsa_circ_40354,RMVar_hsa_circ_98465,RMVar_hsa_circ_196328,RMVar_hsa_circ_196329,RMVar_hsa_circ_324270 70785 RMVar_ID_70785 Human_SNP_ID_670103208 m1A Human chr19 - 55389790 55389790 55389790 CGGGGGGTCCTGAGCAGGTACCAAGTCACCCAACTCAGTTTTAAGGCAACACCTCTCAATCTGAG CGGGGGGTCCTGAGCAGGTACCAAGTCACCCACCTCAGTTTTAAGGCAACACCTCTCAATCTGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55389780..55389893 26863196 MeRIP-seq:(Medium) rs1156804952 Functional Loss SNV dbSNP153 33..33 33 - - - 70786 RMVar_ID_70786 Human_SNP_ID_670103241 m1A Human chr19 - 55389857 55389857 55389857 AGCAGGTACGAAGTCACCAGCGGAGTGAGGCCAGCTGGAGGTGGGCCTGAGTGGGATTGGGACAG AGCAGGTACGAAGTCACCAGCGGAGTGAGGCCGGCTGGAGGTGGGCCTGAGTGGGATTGGGACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55389808..55389891 26863196 MeRIP-seq:(Medium) rs1295062206 Functional Loss SNV dbSNP153 33..33 33 - - - 70787 RMVar_ID_70787 Human_SNP_ID_670107266 m1A Human chr19 + 55401601 55401601 55401601 GAGGAAGCTTCAGTGCCACTGGCCAGGGCCCGACCGGCTTCGGCCCTGCCGCTGGGCCCGCCGGC GAGGAAGCTTCAGTGCCACTGGCCAGGGCCCGCCCGGCTTCGGCCCTGCCGCTGGGCCCGCCGGC A C RPL28 Ensembl:ENSG00000108107 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:55401501..55401646 26863410 MeRIP-seq:(Medium) rs111954966 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70788 RMVar_ID_70788 Human_SNP_ID_670108214 m1A Human chr19 + 55404465 55404465 55404465 AGCAGGAGTTTCATGCGGAACAGACCTCCAGCATATGGGGTCCCCTCTGGAGTGGAGGGAGGGGT AGCAGGAGTTTCATGCGGAACAGACCTCCAGCGTATGGGGTCCCCTCTGGAGTGGAGGGAGGGGT A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:55404368..55404469 26863410 MeRIP-seq:(Medium) rs771806285 Functional Loss SNV dbSNP153 33..33 33 - - - 70789 RMVar_ID_70789 Human_SNP_ID_670109267 m1A Human chr19 - 55407673 55407673 55407673 GGCCGCCGGGGCCTCTCCAGGGCCGCAGCGGCAGCAGTTGGGCCCCCCGCCCCGGCCGGCGGACC GGCCGCCGGGGCCTCTCCAGGGCCGCAGCGGCGGCAGTTGGGCCCCCCGCCCCGGCCGGCGGACC T C UBE2S Ensembl:ENSG00000108106 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:55407626..55407725 32194978 MeRIP-seq:(Medium) rs960011563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53479,Human_RBP_ID_239909,Human_RBP_ID_4557706,Human_RBP_ID_5117132,Human_RBP_ID_5320590,Human_RBP_ID_5443453,Human_RBP_ID_9329214,Human_RBP_ID_17657358 Human_Splice_Rec_2047617,Human_Splice_Rec_2047623,Human_Splice_Rec_2047631 RMVar_hsa_circ_90663,RMVar_hsa_circ_196335 70790 RMVar_ID_70790 Human_SNP_ID_670109289 m1A Human chr19 + 55407730 55407730 55407730 CGGCGGCCCCGCTCCGCTCCCCGCTGCCTCCGACGTCCGCCGCGCACAGCGTAGACCAACCCGCC CGGCGGCCCCGCTCCGCTCCCCGCTGCCTCCGGCGTCCGCCGCGCACAGCGTAGACCAACCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55406853..55407913;chr19:55407626..55407800;chr19:55406876..55407962;chr19:55406853..55407918;chr19:55406876..55407901 26863196 MeRIP-seq:(Medium) rs1351076246 Functional Loss SNV dbSNP153 33..33 33 - - - 70791 RMVar_ID_70791 Human_SNP_ID_670109293 m1A Human chr19 - 55407733 55407733 55407733 GGCGGCGGGTTGGTCTACGCTGTGCGCGGCGGACGTCGGAGGCAGCGGGGAGCGGAGCGGGGCCG GGCGGCGGGTTGGTCTACGCTGTGCGCGGCGGTCGTCGGAGGCAGCGGGGAGCGGAGCGGGGCCG T A UBE2S Ensembl:ENSG00000108106 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:55407563..55407800;chr19:55407626..55407800 26863196 MeRIP-seq:(Medium) rs553108385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527054,Human_RBP_ID_771030,Human_RBP_ID_1571107,Human_RBP_ID_4547336,Human_RBP_ID_5117133,Human_RBP_ID_5320591,Human_RBP_ID_5421844,Human_RBP_ID_8493867,Human_RBP_ID_8837209,Human_RBP_ID_9329215,Human_RBP_ID_18421599,Human_RBP_ID_22447023,Human_RBP_ID_22503688,Human_RBP_ID_22533213,Human_RBP_ID_22812272,Human_RBP_ID_26995400,Human_RBP_ID_27278366 RMVar_hsa_circ_90663,RMVar_hsa_circ_196335 70792 RMVar_ID_70792 Human_SNP_ID_670109294 m1A Human chr19 - 55407733 55407733 55407733 GGCGGCGGGTTGGTCTACGCTGTGCGCGGCGGACGTCGGAGGCAGCGGGGAGCGGAGCGGGGCCG GGCGGCGGGTTGGTCTACGCTGTGCGCGGCGGGCGTCGGAGGCAGCGGGGAGCGGAGCGGGGCCG T C UBE2S Ensembl:ENSG00000108106 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:55407563..55407800;chr19:55407626..55407800 26863196 MeRIP-seq:(Medium) rs553108385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527054,Human_RBP_ID_771030,Human_RBP_ID_1571107,Human_RBP_ID_4547336,Human_RBP_ID_5117133,Human_RBP_ID_5320591,Human_RBP_ID_5421844,Human_RBP_ID_8493867,Human_RBP_ID_8837209,Human_RBP_ID_9329215,Human_RBP_ID_18421599,Human_RBP_ID_22447023,Human_RBP_ID_22503688,Human_RBP_ID_22533213,Human_RBP_ID_22812272,Human_RBP_ID_26995400,Human_RBP_ID_27278366 RMVar_hsa_circ_90663,RMVar_hsa_circ_196335 70793 RMVar_ID_70793 Human_SNP_ID_670117440 m1A Human chr19 - 55435117 55435111 55435117 CACACCATACACATACACCACACACACCACACACACCACACACACACCATACACACACACCACAC CACACCATACACATACACCACACACACCACAC______CACACACACCATACACACACACCACAC GTGGTGT G SHISA7 Ensembl:ENSG00000187902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55435115..55435180 26863196 MeRIP-seq:(Medium) rs1265502276 Functional Loss DEL dbSNP153 33..38 33 - - - 70794 RMVar_ID_70794 Human_SNP_ID_670117451 m1A Human chr19 - 55435117 55435117 55435117 CACACCATACACATACACCACACACACCACACACACCACACACACACCATACACACACACCACAC CACACCATACACATACACCACACACACCACACTCACCACACACACACCATACACACACACCACAC T A SHISA7 Ensembl:ENSG00000187902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55435115..55435180 26863196 MeRIP-seq:(Medium) rs796205798 Functional Loss SNV dbSNP153 33..33 33 - - - 70795 RMVar_ID_70795 Human_SNP_ID_670123419 m1A Human chr19 + 55453134 55453134 55453134 CAGCCAATTCCCACCCAGTTTCCAGGAGTCTCATTTGCATTTCCGGGAGCAGCTGTCCAATGGGA CAGCCAATTCCCACCCAGTTTCCAGGAGTCTCCTTTGCATTTCCGGGAGCAGCTGTCCAATGGGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55453001..55453340 26863196 MeRIP-seq:(Medium) rs935994627 Functional Loss SNV dbSNP153 33..33 33 - - - 70796 RMVar_ID_70796 Human_SNP_ID_670123420 m1A Human chr19 + 55453134 55453134 55453134 CAGCCAATTCCCACCCAGTTTCCAGGAGTCTCATTTGCATTTCCGGGAGCAGCTGTCCAATGGGA CAGCCAATTCCCACCCAGTTTCCAGGAGTCTCGTTTGCATTTCCGGGAGCAGCTGTCCAATGGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55453001..55453340 26863196 MeRIP-seq:(Medium) rs935994627 Functional Loss SNV dbSNP153 33..33 33 - - - 70797 RMVar_ID_70797 Human_SNP_ID_670123498 m1A Human chr19 + 55453276 55453276 55453276 GAACGGGCTTCCACTGAGGTCCGGGTGACAGGAGGGTGGTCTTCCCTCAAGGCAGGGTTGGAGTT GAACGGGCTTCCACTGAGGTCCGGGTGACAGGTGGGTGGTCTTCCCTCAAGGCAGGGTTGGAGTT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55453226..55453300 32194978 MeRIP-seq:(Medium) rs1193678157 Functional Loss SNV dbSNP153 33..33 33 - - - 70798 RMVar_ID_70798 Human_SNP_ID_670124568 m1A Human chr19 + 55456426 55456426 55456426 GATGTTGTGGCGGAACTTCTCCTGCATGTCACACAGGAACAGGACAGAGGATCCTGGGAGGACTC GATGTTGTGGCGGAACTTCTCCTGCATGTCACTCAGGAACAGGACAGAGGATCCTGGGAGGACTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55456376..55456545 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 70799 RMVar_ID_70799 Human_SNP_ID_670126012 m1A Human chr19 + 55461595 55461595 55461595 GGGCACCCTCACCTCTCGGCTCTCGGACGGCCACCGCTGAGGCCTCTTGCGGGCTTCCCAGGGCT GGGCACCCTCACCTCTCGGCTCTCGGACGGCCGCCGCTGAGGCCTCTTGCGGGCTTCCCAGGGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55461462..55461650;chr19:55460020..55461728;chr19:55460020..55461711;chr19:55461466..55461650 26863196 MeRIP-seq:(Medium) rs1475221748 Functional Loss SNV dbSNP153 33..33 33 - - - 70800 RMVar_ID_70800 Human_SNP_ID_670130507 m1A Human chr19 - 55476683 55476664 55476683 CTGTGGGGACCGGGGAGGGGGGGCAGGGGCGCACTCCCTCCCAACGGCCCCCGGCGCGAGGCACC CTGTGGGGACCGGGGAGGGGGGGCAGGGGCGC___________________CGGCGCGAGGCACC GGGGGCCGTTGGGAGGGAGT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55476626..55476772 26863196 MeRIP-seq:(Medium) rs1297715798 Functional Loss DEL dbSNP153 33..51 33 - - - 70801 RMVar_ID_70801 Human_SNP_ID_670130509 m1A Human chr19 - 55476672 55476672 55476672 GGGGAGGGGGGGCAGGGGCGCACTCCCTCCCAACGGCCCCCGGCGCGAGGCACCCAACCTTTATC GGGGAGGGGGGGCAGGGGCGCACTCCCTCCCAGCGGCCCCCGGCGCGAGGCACCCAACCTTTATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55476657..55476768 26863196 MeRIP-seq:(Medium) rs949828006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5500149 70802 RMVar_ID_70802 Human_SNP_ID_670130545 m1A Human chr19 + 55476720 55476720 55476720 CCCTGCCCCCCCTCCCCGGTCCCCACAGCTGCACCGCCGCTGCCGGGGCCCCACCTTCCCGTCGA CCCTGCCCCCCCTCCCCGGTCCCCACAGCTGCCCCGCCGCTGCCGGGGCCCCACCTTCCCGTCGA A C ZNF628 Ensembl:ENSG00000197483 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55476688..55476775 26863196 MeRIP-seq:(Medium) rs968123055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2047705,Human_Splice_Rec_2047709 RMVar_hsa_circ_118910,RMVar_hsa_circ_196336 70803 RMVar_ID_70803 Human_SNP_ID_670131157 m1A Human chr19 + 55478293 55478293 55478293 AATAAGGCAGGAAAAGGGAATGGGGAGTTGGAAGGGATTGTAGATTTAAATAGGGCTGTCAGGGA AATAAGGCAGGAAAAGGGAATGGGGAGTTGGAGGGGATTGTAGATTTAAATAGGGCTGTCAGGGA A G ZNF628 Ensembl:ENSG00000197483 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55478263..55478488 26863196 MeRIP-seq:(Medium) rs139360928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118910,RMVar_hsa_circ_196336 70804 RMVar_ID_70804 Human_SNP_ID_670131373 m1A Human chr19 + 55479135 55479135 55479135 GGTGCCGGAGCCCCGGGCGCTCCCACATCTAGAGGTCAGGGAGGTGAGAAGGAACCAAGCTGGGG GGTGCCGGAGCCCCGGGCGCTCCCACATCTAGGGGTCAGGGAGGTGAGAAGGAACCAAGCTGGGG A G ZNF628 Ensembl:ENSG00000197483 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55479133..55479204 26863196 MeRIP-seq:(Medium) rs1278337878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118910,RMVar_hsa_circ_196336 70805 RMVar_ID_70805 Human_SNP_ID_670132356 m1A Human chr19 + 55482086 55482086 55482086 GGAGACCACGGTGGAGCTGGTGTACCGCTGCGATGGCTGCGAGCAGGGATTCAGCAGCGAGGAGC GGAGACCACGGTGGAGCTGGTGTACCGCTGCGGTGGCTGCGAGCAGGGATTCAGCAGCGAGGAGC A G ZNF628 Ensembl:ENSG00000197483 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55482075..55482216 26863196 MeRIP-seq:(Medium) rs1434232296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5469178,Human_RBP_ID_22070572 RMVar_hsa_circ_118910,RMVar_hsa_circ_196336 70806 RMVar_ID_70806 Human_SNP_ID_670133249 m1A Human chr19 + 55483623 55483623 55483623 ATCGTTCTGCAGAATGTGGGGGGTGGGGAGGCAGGGCCACAGGAAATGAGTGGGGTGCAGCTCCA ATCGTTCTGCAGAATGTGGGGGGTGGGGAGGCGGGGCCACAGGAAATGAGTGGGGTGCAGCTCCA A G ZNF628 Ensembl:ENSG00000197483 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55483591..55483755 26863196 MeRIP-seq:(Medium) rs942769747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22072088 RMVar_hsa_circ_118910,RMVar_hsa_circ_196336 70807 RMVar_ID_70807 Human_SNP_ID_670134420 m1A Human chr19 - 55486475 55486475 55486475 CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGAGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGTGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG T A HSALNG0127668 RNACentral:URS0000E9CC7D lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55486437..55486733 32194978 MeRIP-seq:(Medium) rs78400453 Functional Loss SNV dbSNP153 33..33 33 - - - 70808 RMVar_ID_70808 Human_SNP_ID_670134421 m1A Human chr19 - 55486475 55486475 55486475 CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGAGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGGGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG T C HSALNG0127668 RNACentral:URS0000E9CC7D lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55486437..55486733 32194978 MeRIP-seq:(Medium) rs78400453 Functional Loss SNV dbSNP153 33..33 33 - - - 70809 RMVar_ID_70809 Human_SNP_ID_670134422 m1A Human chr19 - 55486475 55486475 55486475 CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGAGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG CAAAGCGCAGGCCGCTGCTGGCCGCCGCCAGGCGGAGCAGGGCCGGCGGCCGTGTCAAGGCATGG T G HSALNG0127668 RNACentral:URS0000E9CC7D lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55486437..55486733 32194978 MeRIP-seq:(Medium) rs78400453 Functional Loss SNV dbSNP153 33..33 33 - - - 70810 RMVar_ID_70810 Human_SNP_ID_670136404 m1A Human chr19 + 55491083 55491083 55491083 ACAGCGAGGATGCGGGGCTGGTCTGCACCGGTACGTCGGGCTGGGGCCTGGCCCCCTCCTGTCTT ACAGCGAGGATGCGGGGCTGGTCTGCACCGGTTCGTCGGGCTGGGGCCTGGCCCCCTCCTGTCTT A T SSC5D Ensembl:ENSG00000179954 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55491071..55491271 26863196 MeRIP-seq:(Medium) rs1271462861 Functional Loss SNV dbSNP153 33..33 33 - - - 70811 RMVar_ID_70811 Human_SNP_ID_670136648 m1A Human chr19 + 55491919 55491919 55491919 GGAGGCCGGCAGGCAGAGGGCACCCACCTGGCATTTCATCAGCGTTGGGGTGGGGACAGTACACG GGAGGCCGGCAGGCAGAGGGCACCCACCTGGCGTTTCATCAGCGTTGGGGTGGGGACAGTACACG A G SSC5D Ensembl:ENSG00000179954 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55491817..55492117 26863196 MeRIP-seq:(Medium) rs1042894438 Functional Loss SNV dbSNP153 33..33 33 - - - 70812 RMVar_ID_70812 Human_SNP_ID_670139271 m1A Human chr19 + 55500238 55500238 55500238 CGCTGACCCCTCAGGCCCCCCGAGAACGGACCACTAAGACCATGGCAATGCTGACCACTCAAGGC CGCTGACCCCTCAGGCCCCCCGAGAACGGACCTCTAAGACCATGGCAATGCTGACCACTCAAGGC A T SSC5D Ensembl:ENSG00000179954 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55500155..55500305 26863196 MeRIP-seq:(Medium) rs1227215537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36152 70813 RMVar_ID_70813 Human_SNP_ID_670139813 m1A Human chr19 - 55501697 55501697 55501697 CAAGACAGAGGCCATAGAGCAGAGGGGGATGGAGCTGTGGCCCTGGAGGCTGATTCTGCTGGCCA CAAGACAGAGGCCATAGAGCAGAGGGGGATGGCGCTGTGGCCCTGGAGGCTGATTCTGCTGGCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55501689..55501925 26863196 MeRIP-seq:(Medium) rs558299411 Functional Loss SNV dbSNP153 33..33 33 - - - 70814 RMVar_ID_70814 Human_SNP_ID_670139822 m1A Human chr19 - 55501721 55501721 55501721 CAGGTGTGGAAGGAGCTGCAGCAGCAAGACAGAGGCCATAGAGCAGAGGGGGATGGAGCTGTGGC CAGGTGTGGAAGGAGCTGCAGCAGCAAGACAGGGGCCATAGAGCAGAGGGGGATGGAGCTGTGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55501690..55501761 26863196 MeRIP-seq:(Medium) rs1411972190 Functional Loss SNV dbSNP153 33..33 33 - - - 70815 RMVar_ID_70815 Human_SNP_ID_670144185 m1A Human chr19 - 55517383 55517383 55517383 TGTCCGGAGCGTCAGAGGTCGCCTCGGACGTCAAGGCTGAGTGGGGAGTGAGCTCTCGACTGGAG TGTCCGGAGCGTCAGAGGTCGCCTCGGACGTCGAGGCTGAGTGGGGAGTGAGCTCTCGACTGGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55517348..55517556 26863196 MeRIP-seq:(Medium) rs1474777619 Functional Loss SNV dbSNP153 33..33 33 - - - 70816 RMVar_ID_70816 Human_SNP_ID_670144612 m1A Human chr19 - 55518188 55518188 55518188 GTGGTGGGGTAAGGGGTCGTGGTGGGGTCAGGAGTCATGGTGGGGTGAGGGGTTGTGGTGGGGTG GTGGTGGGGTAAGGGGTCGTGGTGGGGTCAGGGGTCATGGTGGGGTGAGGGGTTGTGGTGGGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55518145..55518451 26863196 MeRIP-seq:(Medium) rs1472186933 Functional Loss SNV dbSNP153 33..33 33 - - - 70817 RMVar_ID_70817 Human_SNP_ID_670154815 m1A Human chr19 - 55545905 55545904 55545906 AGACGGGGAGAGAAGGAGACAAAGACGCACAAAGAGAGAGGATAGACGGAGCAAGAGAGAGGCTG AGACGGGGAGAGAAGGAGACAAAGACGCACA__GAGAGAGGATAGACGGAGCAAGAGAGAGGCTG CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55545903..55546269 26863196 MeRIP-seq:(Medium) rs771732340 Functional Loss DEL dbSNP153 32..33 33 - - - 70818 RMVar_ID_70818 Human_SNP_ID_670155051 m1A Human chr19 - 55546711 55546711 55546711 TAGACTCCTGGATCTGAGGGAGGAGGAGCTGGAGGCCTGGACTCTTGGGTCTGAGGGAGGTGGGG TAGACTCCTGGATCTGAGGGAGGAGGAGCTGGGGGCCTGGACTCTTGGGTCTGAGGGAGGTGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55546703..55547066 26863196 MeRIP-seq:(Medium) rs1028660563 Functional Loss SNV dbSNP153 33..33 33 - - - 70819 RMVar_ID_70819 Human_SNP_ID_670155172 m1A Human chr19 - 55547005 55547005 55547005 TGGACTCCTGGGTCTGAGGGAGGAGGAGCTGGAGTCTGGACTCCTGGGTCTGAGGGTGGAGAAAC TGGACTCCTGGGTCTGAGGGAGGAGGAGCTGGGGTCTGGACTCCTGGGTCTGAGGGTGGAGAAAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55546971..55547145 26863196 MeRIP-seq:(Medium) rs1403434203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8493915 70820 RMVar_ID_70820 Human_SNP_ID_670165226 m1A Human chr19 - 55579056 55579056 55579056 GCCCACCAGCGCCGCGGAGCCCCGGGAGTCGGAGTCGGAGGAGGCCGAGGCCGGGGCAGCAGAGC GCCCACCAGCGCCGCGGAGCCCCGGGAGTCGGTGTCGGAGGAGGCCGAGGCCGGGGCAGCAGAGC T A ZNF579 Ensembl:ENSG00000218891 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55579048..55579263 26863196 MeRIP-seq:(Medium) rs1284000414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27158097 RMVar_hsa_circ_78412,RMVar_hsa_circ_196341 70821 RMVar_ID_70821 Human_SNP_ID_670165758 m1A Human chr19 - 55580726 55580726 55580726 AGGCCCAGGGCTGAGAAATCCTCAAGGCCTCGACCCGGCCCCAATTCTGCTGATCATGCCTTCGG AGGCCCAGGGCTGAGAAATCCTCAAGGCCTCGCCCCGGCCCCAATTCTGCTGATCATGCCTTCGG T G ZNF579 Ensembl:ENSG00000218891 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55580721..55580862 26863196 MeRIP-seq:(Medium) rs1009563855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78412,RMVar_hsa_circ_196341 70822 RMVar_ID_70822 Human_SNP_ID_670165762 m1A Human chr19 - 55580734 55580734 55580734 CAAGCCCCAGGCCCAGGGCTGAGAAATCCTCAAGGCCTCGACCCGGCCCCAATTCTGCTGATCAT CAAGCCCCAGGCCCAGGGCTGAGAAATCCTCAGGGCCTCGACCCGGCCCCAATTCTGCTGATCAT T C ZNF579 Ensembl:ENSG00000218891 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55580729..55580827;chr19:55580730..55580825 26863196 MeRIP-seq:(Medium) rs1568510346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78412,RMVar_hsa_circ_196341 70823 RMVar_ID_70823 Human_SNP_ID_670169268 m1A Human chr19 + 55593355 55593355 55593355 CGCGCAGGCGCCGCACGCAAATGGGGGCAAGGAGGCCGCGGCCGCAGCTGCCGCCTCTGCCAGCC CGCGCAGGCGCCGCACGCAAATGGGGGCAAGGCGGCCGCGGCCGCAGCTGCCGCCTCTGCCAGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55593321..55593396 26863196 MeRIP-seq:(Medium) rs1401911559 Functional Loss SNV dbSNP153 33..33 33 - - - 70824 RMVar_ID_70824 Human_SNP_ID_670170466 m1A Human chr19 - 55597808 55597808 55597808 CTGCACCAGCACCGCCCGCCGCTGCCGCCCCCAGGGTCCCGTTTCACTGCAGTGAATGTGGCAAG CTGCACCAGCACCGCCCGCCGCTGCCGCCCCCCGGGTCCCGTTTCACTGCAGTGAATGTGGCAAG T G FIZ1 Ensembl:ENSG00000179943 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55597764..55598236 26863196 MeRIP-seq:(Medium) rs115558748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27471451 Human_Splice_Rec_2047816,Human_Splice_Rec_2047822,Human_Splice_Rec_2047828 RMVar_hsa_circ_106785,RMVar_hsa_circ_97281,RMVar_hsa_circ_196342,RMVar_hsa_circ_196343 70825 RMVar_ID_70825 Human_SNP_ID_670170509 m1A Human chr19 - 55597897 55597897 55597897 CTGCTCCTCTGTCTCCCCACTACTCCAGAGAGAGCCCCCACATACCACTGTATTCCCCGCCACCA CTGCTCCTCTGTCTCCCCACTACTCCAGAGAGGGCCCCCACATACCACTGTATTCCCCGCCACCA T C FIZ1 Ensembl:ENSG00000179943 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55597655..55598323 26863196 MeRIP-seq:(Medium) rs1295215325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18739389 Human_Splice_Rec_2047816,Human_Splice_Rec_2047822,Human_Splice_Rec_2047828 RMVar_hsa_circ_106785,RMVar_hsa_circ_97281,RMVar_hsa_circ_196342,RMVar_hsa_circ_196343 70826 RMVar_ID_70826 Human_SNP_ID_670170775 m1A Human chr19 - 55598976 55598976 55598976 ACTCATTGAGGCTGGTTGGGTAAAGGGAGCCCAGGAAGCAGGAGGGAGGAGTTTAGAGTAGAAGG ACTCATTGAGGCTGGTTGGGTAAAGGGAGCCCTGGAAGCAGGAGGGAGGAGTTTAGAGTAGAAGG T A FIZ1 Ensembl:ENSG00000179943 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55598646..55599624 26863196 MeRIP-seq:(Medium) rs1490053760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826922 RMVar_hsa_circ_106785,RMVar_hsa_circ_97281,RMVar_hsa_circ_196342,RMVar_hsa_circ_196343 70827 RMVar_ID_70827 Human_SNP_ID_670170786 m1A Human chr19 + 55599025 55599025 55599025 ACCAGCCTCAATGAGTTTCCTTCCACCCCTCAATCCAGGGCCTACCCACCATTCCTTCTGAGCCA ACCAGCCTCAATGAGTTTCCTTCCACCCCTCATTCCAGGGCCTACCCACCATTCCTTCTGAGCCA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:55598909..55599038 26863196 MeRIP-seq:(Medium) rs984304890 Functional Loss SNV dbSNP153 33..33 33 - - - 70828 RMVar_ID_70828 Human_SNP_ID_670172267 m1A Human chr19 + 55602808 55602808 55602808 CCGGAGGCCATGGGGGTACCCCTGTGTGCACCAGATCCAGGGTCTGAACCGCCGTGGGACGAGGA CCGGAGGCCATGGGGGTACCCCTGTGTGCACCGGATCCAGGGTCTGAACCGCCGTGGGACGAGGA A G ZNF524 Ensembl:ENSG00000171443 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55602759..55602904 26863196 MeRIP-seq:(Medium) rs780250919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527132 RMVar_hsa_circ_99567,RMVar_hsa_circ_100913,RMVar_hsa_circ_196345,RMVar_hsa_circ_196346 70829 RMVar_ID_70829 Human_SNP_ID_670173150 m1A Human chr19 - 55605692 55605684 55605693 GGGTCTCCGCCGGGAGGAGGCCGAGGAGGCGGAGGAGGCGCCGCCGCTCCGGGGAGACCCGAGGG GGGTCTCCGCCGGGAGGAGGCCGAGGAGGCG_________CCGCCGCTCCGGGGAGACCCGAGGG GCGCCTCCTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55605683..55613774 26863196 MeRIP-seq:(Medium) rs1157421046 Functional Loss DEL dbSNP153 32..40 33 - - - 70830 RMVar_ID_70830 Human_SNP_ID_670173522 m1A Human chr19 - 55606967 55606967 55606967 CACCGTGCTCACCGCCACTTCAGGGCCTTTGCACTTGTTGTTCTTGCTGCCTGCTCACCCAGATC CACCGTGCTCACCGCCACTTCAGGGCCTTTGCCCTTGTTGTTCTTGCTGCCTGCTCACCCAGATC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55606965..55607049 26863196 MeRIP-seq:(Medium) rs918177033 Functional Loss SNV dbSNP153 33..33 33 - - - 70831 RMVar_ID_70831 Human_SNP_ID_670173803 m1A Human chr19 - 55608147 55608140 55608147 CTCACCCCTTCACCTCCTCCCCATCTTTGGTCAACTGTCTTCTCAATGAGCCTCTCAGTAACCAA CTCACCCCTTCACCTCCTCCCCATCTTTGGTC_______TTCTCAATGAGCCTCTCAGTAACCAA AGACAGTT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55608146..55608252 26863196 MeRIP-seq:(Medium) rs1464702932 Functional Loss DEL dbSNP153 33..39 33 - - - 70832 RMVar_ID_70832 Human_SNP_ID_670175577 m1A Human chr19 - 55614409 55614409 55614409 TGTGGCAGCGGCGGTGGCGGATGAGGCTGGACACGTGGTTGTAGGTGCGGCCGCAGACGCCGCAT TGTGGCAGCGGCGGTGGCGGATGAGGCTGGACGCGTGGTTGTAGGTGCGGCCGCAGACGCCGCAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55614358..55614699 26863196 MeRIP-seq:(Medium) rs1337646912 Functional Loss SNV dbSNP153 33..33 33 - - - 70833 RMVar_ID_70833 Human_SNP_ID_670175761 m1A Human chr19 + 55614826 55614826 55614826 TCTGAAGCGCCACGTGAAGACGCACTCGGCCGACCTCCTGCGCCTGCCCTGCGGCATCTGCGGGA TCTGAAGCGCCACGTGAAGACGCACTCGGCCGGCCTCCTGCGCCTGCCCTGCGGCATCTGCGGGA A G ZNF865 Ensembl:ENSG00000261221 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55614820..55614984 26863196 MeRIP-seq:(Medium) rs762125638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8837227,Human_RBP_ID_17931083,Human_RBP_ID_27471461 70834 RMVar_ID_70834 Human_SNP_ID_670175778 m1A Human chr19 - 55614876 55614876 55614876 CGCGTGGGCCGCCTGGTGCTTGAGGAGGTAGGAGGCGTCGCGGAAGGCCTTCCCGCAGATGCCGC CGCGTGGGCCGCCTGGTGCTTGAGGAGGTAGGCGGCGTCGCGGAAGGCCTTCCCGCAGATGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55614827..55614908 26863196 MeRIP-seq:(Medium) rs1456142786 Functional Loss SNV dbSNP153 33..33 33 - - - 70835 RMVar_ID_70835 Human_SNP_ID_670176378 m1A Human chr19 - 55616476 55616476 55616476 GCTCACAGCGGTAGGCGCGCTCGCCCAGGTGCAGCCGCTGGTGCTCCAGCAGGTTGGAGCGGTAG GCTCACAGCGGTAGGCGCGCTCGCCCAGGTGCTGCCGCTGGTGCTCCAGCAGGTTGGAGCGGTAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55616428..55616775 32194978 MeRIP-seq:(Medium) rs778590974 Functional Loss SNV dbSNP153 33..33 33 - - - 70836 RMVar_ID_70836 Human_SNP_ID_670177851 m1A Human chr19 - 55621634 55621634 55621634 GGGACAGAAGAGGGGAGATTGGGGGAGAGATGACAGCTGCAGGGATGGTTGTGAGCCGCTAGTGA GGGACAGAAGAGGGGAGATTGGGGGAGAGATGTCAGCTGCAGGGATGGTTGTGAGCCGCTAGTGA T A ZNF784 Ensembl:ENSG00000179922 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55621477..55624566 26863196 MeRIP-seq:(Medium) rs1269059727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264127,Human_RBP_ID_3588646,Human_RBP_ID_8197966,Human_RBP_ID_22072090,Human_RBP_ID_24552884,Human_RBP_ID_26472924 RMVar_hsa_circ_108860,RMVar_hsa_circ_196348,RMVar_hsa_circ_95286,RMVar_hsa_circ_196347 70837 RMVar_ID_70837 Human_SNP_ID_670178942 m1A Human chr19 + 55624532 55624532 55624532 TGGGATCGCGACTCCGGAGTCGGTGAGCTCCGACTCTGGGCCTCTGGGCGCGCAGCGGCCATCTT TGGGATCGCGACTCCGGAGTCGGTGAGCTCCGCCTCTGGGCCTCTGGGCGCGCAGCGGCCATCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55624410..55624548 26863196 MeRIP-seq:(Medium) rs765037158 Functional Loss SNV dbSNP153 33..33 33 - - - 70838 RMVar_ID_70838 Human_SNP_ID_670178943 m1A Human chr19 + 55624532 55624532 55624532 TGGGATCGCGACTCCGGAGTCGGTGAGCTCCGACTCTGGGCCTCTGGGCGCGCAGCGGCCATCTT TGGGATCGCGACTCCGGAGTCGGTGAGCTCCGGCTCTGGGCCTCTGGGCGCGCAGCGGCCATCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55624410..55624548 26863196 MeRIP-seq:(Medium) rs765037158 Functional Loss SNV dbSNP153 33..33 33 - - - 70839 RMVar_ID_70839 Human_SNP_ID_670181942 m1A Human chr19 + 55635077 55635077 55635077 AGGGAGACCGGGCCGGATTGCGGGGAGTGAGCAGGTTCAGCAGTGACGGCATTCTTAAGAGTCCT AGGGAGACCGGGCCGGATTGCGGGGAGTGAGCGGGTTCAGCAGTGACGGCATTCTTAAGAGTCCT A G ZNF580 Ensembl:ENSG00000213015 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55635026..55635225 26863196 MeRIP-seq:(Medium) rs1012389952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773025,Human_RBP_ID_18420989 70840 RMVar_ID_70840 Human_SNP_ID_670181943 m1A Human chr19 + 55635077 55635077 55635077 AGGGAGACCGGGCCGGATTGCGGGGAGTGAGCAGGTTCAGCAGTGACGGCATTCTTAAGAGTCCT AGGGAGACCGGGCCGGATTGCGGGGAGTGAGCTGGTTCAGCAGTGACGGCATTCTTAAGAGTCCT A T ZNF580 Ensembl:ENSG00000213015 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55635026..55635225 26863196 MeRIP-seq:(Medium) rs1012389952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773025,Human_RBP_ID_18420989 70841 RMVar_ID_70841 Human_SNP_ID_670183586 m1A Human chr19 + 55641048 55641033 55641048 ACTCCGCCAACCCCTCGCACCCCCGCGCCCCCAGTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG ACTCCGCCAACCCCTCGC_______________GTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG CACCCCCGCGCCCCCA C ZNF580,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55641026..55641296 26863196 MeRIP-seq:(Medium) rs1188027157 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_3584036,Human_RBP_ID_4547763,Human_RBP_ID_8196899,Human_RBP_ID_18490972,Human_RBP_ID_26786078 RMVar_hsa_circ_78319,RMVar_hsa_circ_87697,RMVar_hsa_circ_196349,RMVar_hsa_circ_196350 70842 RMVar_ID_70842 Human_SNP_ID_670183601 m1A Human chr19 + 55641048 55641048 55641048 ACTCCGCCAACCCCTCGCACCCCCGCGCCCCCAGTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG ACTCCGCCAACCCCTCGCACCCCCGCGCCCCCCGTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG A C ZNF580,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55641026..55641296 26863196 MeRIP-seq:(Medium) rs895020935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3584036,Human_RBP_ID_4547763,Human_RBP_ID_8196899,Human_RBP_ID_18490972,Human_RBP_ID_26786078 RMVar_hsa_circ_78319,RMVar_hsa_circ_87697,RMVar_hsa_circ_196349,RMVar_hsa_circ_196350 70843 RMVar_ID_70843 Human_SNP_ID_670183602 m1A Human chr19 + 55641048 55641048 55641048 ACTCCGCCAACCCCTCGCACCCCCGCGCCCCCAGTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG ACTCCGCCAACCCCTCGCACCCCCGCGCCCCCGGTCCCCGCGTCCCCGGCGCCGCCGGCCCGGAG A G ZNF580,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55641026..55641296 26863196 MeRIP-seq:(Medium) rs895020935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3584036,Human_RBP_ID_4547763,Human_RBP_ID_8196899,Human_RBP_ID_18490972,Human_RBP_ID_26786078 RMVar_hsa_circ_78319,RMVar_hsa_circ_87697,RMVar_hsa_circ_196349,RMVar_hsa_circ_196350 70844 RMVar_ID_70844 Human_SNP_ID_670183702 m1A Human chr19 + 55641299 55641299 55641299 CCGGGATGGGGGTGGGGGTCGGGAGCGGCAGGATCGGGCGGAGGGACGGGAGGGGAAGTCGAGGC CCGGGATGGGGGTGGGGGTCGGGAGCGGCAGGTTCGGGCGGAGGGACGGGAGGGGAAGTCGAGGC A T ZNF580,CCDC106,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000173581,Ensembl:ENSG00000171425 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:55641248..55641721 26863196 MeRIP-seq:(Medium) rs1318711578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264131,Human_RBP_ID_826574,Human_RBP_ID_3584039,Human_RBP_ID_5370750,Human_RBP_ID_8196901,Human_RBP_ID_8233225,Human_RBP_ID_18945996,Human_RBP_ID_24552886,Human_RBP_ID_26786080 RMVar_hsa_circ_78319,RMVar_hsa_circ_87697,RMVar_hsa_circ_196349,RMVar_hsa_circ_196350 70845 RMVar_ID_70845 Human_SNP_ID_670184104 m1A Human chr19 - 55642586 55642586 55642586 GAGGAGGGGCCTTCCGCCTTGGGGAAAGGGGGAGCCTTGGGGGGCGGTGGGTCCATGGCCTCCGG GAGGAGGGGCCTTCCGCCTTGGGGAAAGGGGGGGCCTTGGGGGGCGGTGGGTCCATGGCCTCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55635706..55648335 26863196 MeRIP-seq:(Medium) rs1260492290 Functional Loss SNV dbSNP153 33..33 33 - - - 70846 RMVar_ID_70846 Human_SNP_ID_670184301 m1A Human chr19 - 55643061 55643061 55643061 TGACGCTGTGTGGGTCAGACTTGGTGGCCCTGAGACGGGCAGGGCAGCACAGGCCGGGTCTCGAG TGACGCTGTGTGGGTCAGACTTGGTGGCCCTGGGACGGGCAGGGCAGCACAGGCCGGGTCTCGAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55642902..55643125 26863196 MeRIP-seq:(Medium) rs974250678 Functional Loss SNV dbSNP153 33..33 33 - - - 70847 RMVar_ID_70847 Human_SNP_ID_670184303 m1A Human chr19 + 55643069 55643066 55643069 CCGGCCTGTGCTGCCCTGCCCGTCTCAGGGCCACCAAGTCTGACCCACACAGCGTCACTCACTCC CCGGCCTGTGCTGCCCTGCCCGTCTCAGGG___CCAAGTCTGACCCACACAGCGTCACTCACTCC GCCA G ZNF580,CCDC106,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000173581,Ensembl:ENSG00000171425 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:55643020..55643220 32194978 MeRIP-seq:(Medium) rs918754761 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_527162,Human_RBP_ID_772056,Human_RBP_ID_3584048,Human_RBP_ID_17082073,Human_RBP_ID_17270643,Human_RBP_ID_17657374,Human_RBP_ID_18165867,Human_RBP_ID_18947363,Human_RBP_ID_26816336,Human_RBP_ID_27471511 Human_miRNA_ID_940043,Human_miRNA_ID_2076661,Human_miRNA_ID_2076662,Human_miRNA_ID_2427785,Human_miRNA_ID_2427786,Human_miRNA_ID_2745900,Human_miRNA_ID_2745901 RMVar_hsa_circ_78319,RMVar_hsa_circ_87697,RMVar_hsa_circ_196349,RMVar_hsa_circ_196350 70848 RMVar_ID_70848 Human_SNP_ID_670184854 m1A Human chr19 + 55644610 55644610 55644610 GTGCTGCCATCCCCCTGCCCTCAGCCTCTGGCATTTTCCTCCGTTGAGACCATGGAGGGCCCTCC GTGCTGCCATCCCCCTGCCCTCAGCCTCTGGCTTTTTCCTCCGTTGAGACCATGGAGGGCCCTCC A T CCDC106,ZNF581 Ensembl:ENSG00000173581,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:55644576..55644650 26863196 MeRIP-seq:(Medium) rs1266839596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527180,Human_RBP_ID_4547830,Human_RBP_ID_5469191,Human_RBP_ID_18192509,Human_RBP_ID_26995498 Human_Splice_Rec_2047852,Human_Splice_Rec_2047854,Human_Splice_Rec_2047856,Human_Splice_Rec_2047858 Human_miRNA_ID_3078917,Human_miRNA_ID_3122184 RMVar_hsa_circ_78319,RMVar_hsa_circ_104333,RMVar_hsa_circ_196349,RMVar_hsa_circ_112732,RMVar_hsa_circ_196351,RMVar_hsa_circ_196352 70849 RMVar_ID_70849 Human_SNP_ID_670184940 m1A Human chr19 + 55644823 55644823 55644823 GAGCCAGGGGCCAGTGGGGCTCCAGGCCAGAAAAAGTGCTACAGCTGCCCCGTGTGCTCAAGGGT GAGCCAGGGGCCAGTGGGGCTCCAGGCCAGAAGAAGTGCTACAGCTGCCCCGTGTGCTCAAGGGT A G CCDC106,ZNF581 Ensembl:ENSG00000173581,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55644726..55644875 26863196 MeRIP-seq:(Medium) rs766197275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78319,RMVar_hsa_circ_104333,RMVar_hsa_circ_196349,RMVar_hsa_circ_112732,RMVar_hsa_circ_196351,RMVar_hsa_circ_196352 70850 RMVar_ID_70850 Human_SNP_ID_670187896 m1A Human chr19 - 55652767 55652767 55652767 CCGGGGTCCACGGGGGAGGAAGGCCCGGGTGGAGGCGCGGAGGCGTGGTGCGATCACCGCTTGAA CCGGGGTCCACGGGGGAGGAAGGCCCGGGTGGGGGCGCGGAGGCGTGGTGCGATCACCGCTTGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55652717..55652816 26863196 MeRIP-seq:(Medium) rs1219334506 Functional Loss SNV dbSNP153 33..33 33 - - - 70851 RMVar_ID_70851 Human_SNP_ID_670187897 m1A Human chr19 - 55652767 55652767 55652767 CCGGGGTCCACGGGGGAGGAAGGCCCGGGTGGAGGCGCGGAGGCGTGGTGCGATCACCGCTTGAA CCGGGGTCCACGGGGGAGGAAGGCCCGGGTGGCGGCGCGGAGGCGTGGTGCGATCACCGCTTGAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55652717..55652816 26863196 MeRIP-seq:(Medium) rs1219334506 Functional Loss SNV dbSNP153 33..33 33 - - - 70852 RMVar_ID_70852 Human_SNP_ID_670187924 m1A Human chr19 - 55652817 55652817 55652817 GAGCGAGGAGGAGGGGCAGGGGCGCGGCGGGGAGAGGGGCAGGTCATCCACCGGGGTCCACGGGG GAGCGAGGAGGAGGGGCAGGGGCGCGGCGGGGGGAGGGGCAGGTCATCCACCGGGGTCCACGGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55652815..55653086 26863196 MeRIP-seq:(Medium) rs979145736 Functional Loss SNV dbSNP153 33..33 33 - - - 70853 RMVar_ID_70853 Human_SNP_ID_670188562 m1A Human chr19 + 55654262 55654262 55654262 GGCCCTTTTTTTCTTTCACTTTCCCCACCCGGAGAGCCAGGTGCCGAGAACTAGGACCTCGTCCC GGCCCTTTTTTTCTTTCACTTTCCCCACCCGGTGAGCCAGGTGCCGAGAACTAGGACCTCGTCCC A T U2AF2 Ensembl:ENSG00000063244 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55654173..55654298 26863410 MeRIP-seq:(Medium) rs1343431961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54838,Human_RBP_ID_1571227,Human_RBP_ID_5421859,Human_RBP_ID_5443459,Human_RBP_ID_5500167,Human_RBP_ID_17931127,Human_RBP_ID_18739450,Human_RBP_ID_22070589,Human_RBP_ID_22592611,Human_RBP_ID_24545539 70854 RMVar_ID_70854 Human_SNP_ID_670188608 m1A Human chr19 + 55654393 55654393 55654393 GAAGGAGCCGAGGTACCCACGGAAAAAGTCGAAGCTGTCCCCGGAGAGTGAGGCCTTCACGAAGC GAAGGAGCCGAGGTACCCACGGAAAAAGTCGACGCTGTCCCCGGAGAGTGAGGCCTTCACGAAGC A C U2AF2 Ensembl:ENSG00000063244 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55654343..55654443 32194978 MeRIP-seq:(Medium) rs1568545567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527220,Human_RBP_ID_1571228,Human_RBP_ID_4547991,Human_RBP_ID_18739451,Human_RBP_ID_23807533,Human_RBP_ID_26995520 70855 RMVar_ID_70855 Human_SNP_ID_670188707 m1A Human chr19 + 55654676 55654676 55654676 AAGCCAAAGACTGGGACGGATTGAATTGTTGGAAGAACCCGAACTCGCAGAGGGGACTGGGCGCA AAGCCAAAGACTGGGACGGATTGAATTGTTGGGAGAACCCGAACTCGCAGAGGGGACTGGGCGCA A G U2AF2 Ensembl:ENSG00000063244 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55654126..55654831 26863196 MeRIP-seq:(Medium) rs897840411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1191572,Human_RBP_ID_1571234,Human_RBP_ID_1891857,Human_RBP_ID_3576520,Human_RBP_ID_9341121,Human_RBP_ID_13511014,Human_RBP_ID_22070591,Human_RBP_ID_26334965,Human_RBP_ID_27278528,Human_RBP_ID_27471548 70856 RMVar_ID_70856 Human_SNP_ID_670188888 m1A Human chr19 - 55655076 55655076 55655076 ACATGCTGAGGCGGCCGCGTAGGGCCCTGTGCAGCTTTCGCCTCGCCTTGCCGCCCGCTCCAGCC ACATGCTGAGGCGGCCGCGTAGGGCCCTGTGCGGCTTTCGCCTCGCCTTGCCGCCCGCTCCAGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55655051..55655075;chr19:55654926..55655197;chr19:55654926..55655194;chr19:55654926..55655201 26863196 MeRIP-seq:(Medium) rs1457128147 Functional Loss SNV dbSNP153 33..33 33 - - - 70857 RMVar_ID_70857 Human_SNP_ID_670188889 m1A Human chr19 - 55655076 55655076 55655076 ACATGCTGAGGCGGCCGCGTAGGGCCCTGTGCAGCTTTCGCCTCGCCTTGCCGCCCGCTCCAGCC ACATGCTGAGGCGGCCGCGTAGGGCCCTGTGCCGCTTTCGCCTCGCCTTGCCGCCCGCTCCAGCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:55655051..55655075;chr19:55654926..55655197;chr19:55654926..55655194;chr19:55654926..55655201 26863196 MeRIP-seq:(Medium) rs1457128147 Functional Loss SNV dbSNP153 33..33 33 - - - 70858 RMVar_ID_70858 Human_SNP_ID_670188915 m1A Human chr19 + 55655102 55655102 55655102 GAAAGCTGCACAGGGCCCTACGCGGCCGCCTCAGCATGTCGGACTTCGACGAGTTCGAGCGGCAG GAAAGCTGCACAGGGCCCTACGCGGCCGCCTCGGCATGTCGGACTTCGACGAGTTCGAGCGGCAG A G U2AF2 Ensembl:ENSG00000063244 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55655001..55655200 26863410 MeRIP-seq:(Medium) rs1317089791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240941,Human_RBP_ID_527222,Human_RBP_ID_1571242,Human_RBP_ID_4548032,Human_RBP_ID_8494016,Human_RBP_ID_9294575,Human_RBP_ID_13511028,Human_RBP_ID_22503700,Human_RBP_ID_22976152,Human_RBP_ID_23807535,Human_RBP_ID_25434025 Human_Splice_Rec_2047919,Human_Splice_Rec_2047941,Human_Splice_Rec_2047961,Human_Splice_Rec_2047969 70859 RMVar_ID_70859 Human_SNP_ID_670190475 m1A Human chr19 + 55659164 55659164 55659164 AGCCACCAGCGCGCAGGGTGGGCTGGGCCCGCATCCTTACTCCGCTTATCCCGTGCCCCTCCTCT AGCCACCAGCGCGCAGGGTGGGCTGGGCCCGCGTCCTTACTCCGCTTATCCCGTGCCCCTCCTCT A G U2AF2 Ensembl:ENSG00000063244 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:55659157..55659394;chr19:55659155..55659408 26863196 MeRIP-seq:(Medium) rs1362753468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908934,Human_RBP_ID_26786088 70860 RMVar_ID_70860 Human_SNP_ID_670190477 m1A Human chr19 + 55659170 55659170 55659170 CAGCGCGCAGGGTGGGCTGGGCCCGCATCCTTACTCCGCTTATCCCGTGCCCCTCCTCTCACCCT CAGCGCGCAGGGTGGGCTGGGCCCGCATCCTTGCTCCGCTTATCCCGTGCCCCTCCTCTCACCCT A G U2AF2 Ensembl:ENSG00000063244 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55659168..55659380 26863196 MeRIP-seq:(Medium) rs1348782264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908934,Human_RBP_ID_26786088 70861 RMVar_ID_70861 Human_SNP_ID_670190915 m1A Human chr19 - 55660254 55660252 55660254 GCACGGGCGTGAGGAAGGTGAAGGGAGTGGACATCAGGGAGGAAGGGGCAGGAAGAGAAGCTCAC GCACGGGCGTGAGGAAGGTGAAGGGAGTGGAC__CAGGGAGGAAGGGGCAGGAAGAGAAGCTCAC GAT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55660251..55660275 26863196 MeRIP-seq:(Medium) rs1409048542 Functional Loss DEL dbSNP153 33..34 33 - - - 70862 RMVar_ID_70862 Human_SNP_ID_670190995 m1A Human chr19 - 55660466 55660466 55660466 GGAGAGCGGGGCAGGGCAACCTCAGTCTGACCAACAGTGGGCCTGCGAGCCCCCTCCCAGGCACC GGAGAGCGGGGCAGGGCAACCTCAGTCTGACCCACAGTGGGCCTGCGAGCCCCCTCCCAGGCACC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:55660462..55660652 26863196 MeRIP-seq:(Medium) rs755880440 Functional Loss SNV dbSNP153 33..33 33 - - - 70863 RMVar_ID_70863 Human_SNP_ID_670191238 m1A Human chr19 - 55661010 55661009 55661010 CGCAGCTTCAAAGGGAATAAAAGCCGGATAAAACCCCATCAGGGGAATGCTCAGTGACCACCCCT CGCAGCTTCAAAGGGAATAAAAGCCGGATAAA_CCCCATCAGGGGAATGCTCAGTGACCACCCCT GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:55661005..55661400;chr19:55661005..55661397 26863196 MeRIP-seq:(Medium) rs1215566232 Functional Loss DEL dbSNP153 33..33 33 - - - 70864 RMVar_ID_70864 Human_SNP_ID_670191243 m1A Human chr19 - 55661022 55661022 55661022 TGGAATCTGACCCGCAGCTTCAAAGGGAATAAAAGCCGGATAAAACCCCATCAGGGGAATGCTCA TGGAATCTGACCCGCAGCTTCAAAGGGAATAACAGCCGGATAAAACCCCATCAGGGGAATGCTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55661017..55661384 26863196 MeRIP-seq:(Medium) rs1442482652 Functional Loss SNV dbSNP153 33..33 33 - - - 70865 RMVar_ID_70865 Human_SNP_ID_670191583 m1A Human chr19 + 55661884 55661884 55661884 TTTCTCAACCTGCACTTTGCTACATTTGATAAACCAGCCCCCGGACTCCAGGGCCAGATTCCTCC TTTCTCAACCTGCACTTTGCTACATTTGATAATCCAGCCCCCGGACTCCAGGGCCAGATTCCTCC A T U2AF2 Ensembl:ENSG00000063244 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55661880..55662328 26863196 MeRIP-seq:(Medium) rs1318049326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1191582,Human_RBP_ID_22546964,Human_RBP_ID_25434159 RMVar_hsa_circ_33716,RMVar_hsa_circ_96892,RMVar_hsa_circ_278616,RMVar_hsa_circ_102765,RMVar_hsa_circ_196354,RMVar_hsa_circ_112393,RMVar_hsa_circ_196355,RMVar_hsa_circ_196356 70866 RMVar_ID_70866 Human_SNP_ID_670191841 m1A Human chr19 - 55662459 55662459 55662459 AATAGGAGACAAGGGGGGGGGCGGGGGAAGGGAGGTGGAGAGAGGAGGGGAAGGGTGAGAGAGGG AATAGGAGACAAGGGGGGGGGCGGGGGAAGGGGGGTGGAGAGAGGAGGGGAAGGGTGAGAGAGGG T C AC008735.2 Ensembl:ENSG00000267523 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55662452..55662531 26863196 MeRIP-seq:(Medium) rs1568550869 Functional Loss SNV dbSNP153 33..33 33 - - - 70867 RMVar_ID_70867 Human_SNP_ID_670195876 m1A Human chr19 + 55674349 55674349 55674349 AGAGGGAAGGGGTTGGGATGGGGACAGGGTGCACAGCAGGGCGGGGTAGGACCCCAGCCCCTCCC AGAGGGAAGGGGTTGGGATGGGGACAGGGTGCCCAGCAGGGCGGGGTAGGACCCCAGCCCCTCCC A C U2AF2 Ensembl:ENSG00000063244 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55674226..55674700 26863196 MeRIP-seq:(Medium) rs1040870974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239072,Human_RBP_ID_527269,Human_RBP_ID_5117146,Human_RBP_ID_5145448,Human_RBP_ID_6784442,Human_RBP_ID_8197978,Human_RBP_ID_9426463,Human_RBP_ID_17655391,Human_RBP_ID_17696408,Human_RBP_ID_17931162,Human_RBP_ID_18193210,Human_RBP_ID_18946015,Human_RBP_ID_22812339,Human_RBP_ID_23131805,Human_RBP_ID_25434275,Human_RBP_ID_26472930,Human_RBP_ID_26786092,Human_RBP_ID_26995619,Human_RBP_ID_27278578 Human_miRNA_ID_2381589,Human_miRNA_ID_2513291,Human_miRNA_ID_3024599,Human_miRNA_ID_3056110 RMVar_hsa_circ_96892,RMVar_hsa_circ_102765,RMVar_hsa_circ_196354,RMVar_hsa_circ_112393,RMVar_hsa_circ_196355,RMVar_hsa_circ_196356,RMVar_hsa_circ_92487,RMVar_hsa_circ_196358,RMVar_hsa_circ_196360,RMVar_hsa_circ_120122,RMVar_hsa_circ_196362,RMVar_hsa_circ_95107 70868 RMVar_ID_70868 Human_SNP_ID_670195963 m1A Human chr19 - 55674568 55674568 55674568 TAAAGAGGAAAAATCAACTACGTAAGAAACCCAGGAGGGGACCAGAGAGGACCAGAGGCCGAAGG TAAAGAGGAAAAATCAACTACGTAAGAAACCCGGGAGGGGACCAGAGAGGACCAGAGGCCGAAGG T C AC008735.2 Ensembl:ENSG00000267523 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55674551..55674575 26863196 MeRIP-seq:(Medium) rs1048318132 Functional Loss SNV dbSNP153 33..33 33 - - - 70869 RMVar_ID_70869 Human_SNP_ID_670195964 m1A Human chr19 - 55674568 55674568 55674568 TAAAGAGGAAAAATCAACTACGTAAGAAACCCAGGAGGGGACCAGAGAGGACCAGAGGCCGAAGG TAAAGAGGAAAAATCAACTACGTAAGAAACCCCGGAGGGGACCAGAGAGGACCAGAGGCCGAAGG T G AC008735.2 Ensembl:ENSG00000267523 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55674551..55674575 26863196 MeRIP-seq:(Medium) rs1048318132 Functional Loss SNV dbSNP153 33..33 33 - - - 70870 RMVar_ID_70870 Human_SNP_ID_670196334 m1A Human chr19 - 55675257 55675257 55675257 GCCCAGAAGGGGCGCGGAGAGCCGGGCGGGGGAGGGGAGCCGCCGAGGAGACGGGAAGCAACAGA GCCCAGAAGGGGCGCGGAGAGCCGGGCGGGGGGGGGGAGCCGCCGAGGAGACGGGAAGCAACAGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55675201..55675450 26863196 MeRIP-seq:(Medium) rs891767498 Functional Loss SNV dbSNP153 33..33 33 - - - 70871 RMVar_ID_70871 Human_SNP_ID_670196405 m1A Human chr19 + 55675387 55675387 55675387 GCACGTCCCGCGACACCGAGGCCGAGCGGGGCAGGGGGCTGACCGCCATGACCCCCCAGAGCCCG GCACGTCCCGCGACACCGAGGCCGAGCGGGGCGGGGGGCTGACCGCCATGACCCCCCAGAGCCCG A G EPN1 Ensembl:ENSG00000063245 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:55675201..55676665;chr19:55675201..55675450 26863196 MeRIP-seq:(Medium) rs1290100835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557720,Human_RBP_ID_9330284,Human_RBP_ID_18192512 Human_Splice_Rec_2048013,Human_Splice_Rec_2048033 Human_miRNA_ID_2152368,Human_miRNA_ID_2420829 RMVar_hsa_circ_89787,RMVar_hsa_circ_196363 70872 RMVar_ID_70872 Human_SNP_ID_670196422 m1A Human chr19 + 55675412 55675412 55675412 GCGGGGCAGGGGGCTGACCGCCATGACCCCCCAGAGCCCGGCGTGAGGGGGCCGAGGTGAGCGCG GCGGGGCAGGGGGCTGACCGCCATGACCCCCCCGAGCCCGGCGTGAGGGGGCCGAGGTGAGCGCG A C EPN1 Ensembl:ENSG00000063245 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55675326..55675450 32194978 MeRIP-seq:(Medium) rs937400972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239075,Human_RBP_ID_4557721,Human_RBP_ID_18192512 Human_Splice_Rec_2048013,Human_Splice_Rec_2048033 Human_miRNA_ID_2425710,Human_miRNA_ID_2435379,Human_miRNA_ID_3070216 RMVar_hsa_circ_89787,RMVar_hsa_circ_196363 70873 RMVar_ID_70873 Human_SNP_ID_670197408 m1A Human chr19 + 55678577 55678577 55678577 ACCTGCCGCAGCCTTCGTCCGGGAGTCGCCCCATCTCTCCACGCATCGGGGCCCTGTGCCCCTTG ACCTGCCGCAGCCTTCGTCCGGGAGTCGCCCCGTCTCTCCACGCATCGGGGCCCTGTGCCCCTTG A G EPN1 Ensembl:ENSG00000063245 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55678482..55678655 26863196 MeRIP-seq:(Medium) rs1242606416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137153,Human_RBP_ID_4548163,Human_RBP_ID_17931176,Human_RBP_ID_18192513,Human_RBP_ID_18441994,Human_RBP_ID_20420456,Human_RBP_ID_26816341,Human_RBP_ID_26995627 Human_Splice_Rec_2048014,Human_Splice_Rec_2048034,Human_Splice_Rec_2048054 Human_miRNA_ID_2137680,Human_miRNA_ID_2137681,Human_miRNA_ID_2610291,Human_miRNA_ID_2610292,Human_miRNA_ID_2666461,Human_miRNA_ID_2666462 RMVar_hsa_circ_89787,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196363,RMVar_hsa_circ_332992,RMVar_hsa_circ_196364,RMVar_hsa_circ_196365 70874 RMVar_ID_70874 Human_SNP_ID_670199656 m1A Human chr19 + 55685496 55685496 55685496 CATGTACGCCGTGCAGACGCTGAAGGACTTCCAGTACGTGGACCGCGACGGCAAGGACCAGGGCG CATGTACGCCGTGCAGACGCTGAAGGACTTCCGGTACGTGGACCGCGACGGCAAGGACCAGGGCG A G EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55685451..55685550 26863196 MeRIP-seq:(Medium) rs1334683759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1295800,Human_RBP_ID_1571344,Human_RBP_ID_1891914,Human_RBP_ID_6784500,Human_RBP_ID_8837281,Human_RBP_ID_13511901,Human_RBP_ID_18192516,Human_RBP_ID_18739557 RMVar_hsa_circ_9292,RMVar_hsa_circ_89787,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196363,RMVar_hsa_circ_332992,RMVar_hsa_circ_196364,RMVar_hsa_circ_196365,RMVar_hsa_circ_331802 70875 RMVar_ID_70875 Human_SNP_ID_670199714 m1A Human chr19 - 55685610 55685610 55685610 TGGCGGTCTGTGCCAGCTTTTCCTTGGTCTTGAGCGCGTGCGCCCGCTCTTCCCGCAGCCGGTCC TGGCGGTCTGTGCCAGCTTTTCCTTGGTCTTGGGCGCGTGCGCCCGCTCTTCCCGCAGCCGGTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55685401..55689375 26863196 MeRIP-seq:(Medium) rs1225615885 Functional Loss SNV dbSNP153 33..33 33 - - - 70876 RMVar_ID_70876 Human_SNP_ID_670201886 m1A Human chr19 - 55691840 55691840 55691840 TCCGAGGTGGGGGCAGCCGTGGGGACGGCAGCAGCCATGGGTGCTGGGCCCCCCCAGGGGTCTGT TCCGAGGTGGGGGCAGCCGTGGGGACGGCAGCCGCCATGGGTGCTGGGCCCCCCCAGGGGTCTGT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55691751..55691918 26863196 MeRIP-seq:(Medium) rs1306848444 Functional Loss SNV dbSNP153 33..33 33 - - - 70877 RMVar_ID_70877 Human_SNP_ID_670202307 m1A Human chr19 + 55692765 55692765 55692765 GCCCCGGCCTTCTCAGATCCCTGGGGAGGGTCACCTGCCAAGCCCAGCACCAATGGCACAACAGG GCCCCGGCCTTCTCAGATCCCTGGGGAGGGTCTCCTGCCAAGCCCAGCACCAATGGCACAACAGG A T EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55692701..55692800 32194978 MeRIP-seq:(Medium) rs771266849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955637,Human_RBP_ID_17657379,Human_RBP_ID_18739561 Human_Splice_Rec_2048026,Human_Splice_Rec_2048027,Human_Splice_Rec_2048044,Human_Splice_Rec_2048045,Human_Splice_Rec_2048064,Human_Splice_Rec_2048065,Human_Splice_Rec_2048079,Human_Splice_Rec_2048081 RMVar_hsa_circ_9292,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196364,RMVar_hsa_circ_331802,RMVar_hsa_circ_100870,RMVar_hsa_circ_95411,RMVar_hsa_circ_196366,RMVar_hsa_circ_196367 70878 RMVar_ID_70878 Human_SNP_ID_670202451 m1A Human chr19 - 55693022 55693022 55693022 GGAGGGCAGGGGCTCACCTGCGCTGCTCCCGGAGGTCGGCAGTGCCGTGCGGAGTCGGTCAAAGT GGAGGGCAGGGGCTCACCTGCGCTGCTCCCGGCGGTCGGCAGTGCCGTGCGGAGTCGGTCAAAGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55692976..55693050 32194978 MeRIP-seq:(Medium) rs748866021 Functional Loss SNV dbSNP153 33..33 33 - - - 70879 RMVar_ID_70879 Human_SNP_ID_670203297 m1A Human chr19 + 55695220 55695220 55695220 GCCCGCGCCTCCCGCGACGCTCACCCTGAACCAGCTCCGTCTCAGTCCTGTGCCTCCCGTCCCTG GCCCGCGCCTCCCGCGACGCTCACCCTGAACCGGCTCCGTCTCAGTCCTGTGCCTCCCGTCCCTG A G EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr19:55695126..55695350;chr19:55695176..55695325 26863196 MeRIP-seq:(Medium) rs745969891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769900,Human_RBP_ID_4548246,Human_RBP_ID_17387061,Human_RBP_ID_18947390 Human_Splice_Rec_2048032,Human_Splice_Rec_2048050,Human_Splice_Rec_2048070 RMVar_hsa_circ_100870,RMVar_hsa_circ_196367 70880 RMVar_ID_70880 Human_SNP_ID_670203301 m1A Human chr19 - 55695227 55695227 55695227 GGCGCTCCAGGGACGGGAGGCACAGGACTGAGACGGAGCTGGTTCAGGGTGAGCGTCGCGGGAGG GGCGCTCCAGGGACGGGAGGCACAGGACTGAGGCGGAGCTGGTTCAGGGTGAGCGTCGCGGGAGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:55695109..55695332 26863196 MeRIP-seq:(Medium) rs769050768 Functional Loss SNV dbSNP153 33..33 33 - - - 70881 RMVar_ID_70881 Human_SNP_ID_670203310 m1A Human chr19 + 55695254 55695254 55695254 CTCCGTCTCAGTCCTGTGCCTCCCGTCCCTGGAGCGCCACCCACGTACATCTCTCCCCTTGGCGG CTCCGTCTCAGTCCTGTGCCTCCCGTCCCTGGCGCGCCACCCACGTACATCTCTCCCCTTGGCGG A C EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:55695125..55695285 26863410 MeRIP-seq:(Medium) rs1345210300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527291,Human_RBP_ID_17387061,Human_RBP_ID_18192518,Human_RBP_ID_18947390 RMVar_hsa_circ_100870,RMVar_hsa_circ_196367 70882 RMVar_ID_70882 Human_SNP_ID_670203351 m1A Human chr19 + 55695306 55695306 55695306 CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCATGATGCCCCCGGGCCCCCCGGCCCCCAACACT CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCCTGATGCCCCCGGGCCCCCCGGCCCCCAACACT A C EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55695106..55695725 26863196 MeRIP-seq:(Medium) rs755464988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527293,Human_RBP_ID_4548250,Human_RBP_ID_17387062,Human_RBP_ID_17657381,Human_RBP_ID_18192518,Human_RBP_ID_18947391,Human_RBP_ID_22976225 Human_miRNA_ID_2277236 RMVar_hsa_circ_100870,RMVar_hsa_circ_196367 70883 RMVar_ID_70883 Human_SNP_ID_670203352 m1A Human chr19 + 55695306 55695306 55695306 CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCATGATGCCCCCGGGCCCCCCGGCCCCCAACACT CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCGTGATGCCCCCGGGCCCCCCGGCCCCCAACACT A G EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55695106..55695725 26863196 MeRIP-seq:(Medium) rs755464988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527293,Human_RBP_ID_4548250,Human_RBP_ID_17387062,Human_RBP_ID_17657381,Human_RBP_ID_18192518,Human_RBP_ID_18947391,Human_RBP_ID_22976225 Human_miRNA_ID_2277236 RMVar_hsa_circ_100870,RMVar_hsa_circ_196367 70884 RMVar_ID_70884 Human_SNP_ID_670299414 m1A Human chr19 - 55993507 55993496 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG___________GGGGGGAGAGGGGGAGGGAGGG CTCCCCTCCTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475706 Functional Loss DEL dbSNP153 33..43 33 - - - 70885 RMVar_ID_70885 Human_SNP_ID_670299425 m1A Human chr19 - 55993507 55993499 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG________GGAGGGGGGAGAGGGGGAGGGAGGG CCCTCCTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475736 Functional Loss DEL dbSNP153 33..40 33 - - - 70886 RMVar_ID_70886 Human_SNP_ID_670299429 m1A Human chr19 - 55993507 55993500 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG_______GGGAGGGGGGAGAGGGGGAGGGAGGG CCTCCTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475741 Functional Loss DEL dbSNP153 33..39 33 - - - 70887 RMVar_ID_70887 Human_SNP_ID_670299433 m1A Human chr19 - 55993507 55993501 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG______GGGGAGGGGGGAGAGGGGGAGGGAGGG CTCCTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475754 Functional Loss DEL dbSNP153 33..38 33 - - - 70888 RMVar_ID_70888 Human_SNP_ID_670299437 m1A Human chr19 - 55993507 55993502 55993508 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGG______AGGGGAGGGGGGAGAGGGGGAGGGAGGG TCCTCTC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475764 Functional Loss DEL dbSNP153 32..37 33 - - - 70889 RMVar_ID_70889 Human_SNP_ID_670299440 m1A Human chr19 - 55993507 55993503 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG____GAGGGGAGGGGGGAGAGGGGGAGGGAGGG CCTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475765 Functional Loss DEL dbSNP153 33..36 33 - - - 70890 RMVar_ID_70890 Human_SNP_ID_670299441 m1A Human chr19 - 55993507 55993503 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG__AGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG CCTCT CCT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475765 Functional Loss DEL dbSNP153 33..34 33 - - - 70891 RMVar_ID_70891 Human_SNP_ID_670299444 m1A Human chr19 - 55993507 55993504 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG___GGAGGGGAGGGGGGAGAGGGGGAGGGAGGG CTCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475774 Functional Loss DEL dbSNP153 33..35 33 - - - 70892 RMVar_ID_70892 Human_SNP_ID_670299447 m1A Human chr19 - 55993507 55993505 55993508 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGG___AGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG TCTC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475777 Functional Loss DEL dbSNP153 32..34 33 - - - 70893 RMVar_ID_70893 Human_SNP_ID_670299452 m1A Human chr19 - 55993507 55993506 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGG_GAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1568475782 Functional Loss DEL dbSNP153 33..33 33 - - - 70894 RMVar_ID_70894 Human_SNP_ID_670299453 m1A Human chr19 - 55993507 55993507 55993507 AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG AGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGGGAGGAGGGGAGGGGGGAGAGGGGGAGGGAGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55993451..55993634 26863196 MeRIP-seq:(Medium) rs1348374460 Functional Loss SNV dbSNP153 33..33 33 - - - 70895 RMVar_ID_70895 Human_SNP_ID_670299515 m1A Human chr19 - 55993526 55993522 55993526 GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGG____GGGAGGGGAGGGGGGAGAGGAGGGGAGGG CCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55993505..55993636 26863196 MeRIP-seq:(Medium) rs1568475874 Functional Loss DEL dbSNP153 33..36 33 - - - 70896 RMVar_ID_70896 Human_SNP_ID_670299518 m1A Human chr19 - 55993526 55993523 55993526 GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGG___GGGGAGGGGAGGGGGGAGAGGAGGGGAGGG CCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55993505..55993636 26863196 MeRIP-seq:(Medium) rs1568475883 Functional Loss DEL dbSNP153 33..35 33 - - - 70897 RMVar_ID_70897 Human_SNP_ID_670299520 m1A Human chr19 - 55993526 55993524 55993526 GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGG__GGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG CCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55993505..55993636 26863196 MeRIP-seq:(Medium) rs1568475888 Functional Loss DEL dbSNP153 33..34 33 - - - 70898 RMVar_ID_70898 Human_SNP_ID_670299523 m1A Human chr19 - 55993526 55993525 55993526 GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGG_GGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55993505..55993636 26863196 MeRIP-seq:(Medium) rs201829003 Functional Loss DEL dbSNP153 33..33 33 - - - 70899 RMVar_ID_70899 Human_SNP_ID_670299525 m1A Human chr19 - 55993526 55993526 55993526 GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGAGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG GGAGGGGGAGGGGGAGGGGAGGGGGGGAGGGGGGGGGGGAGGGGAGGGGGGAGAGGAGGGGAGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55993505..55993636 26863196 MeRIP-seq:(Medium) rs1195821043 Functional Loss SNV dbSNP153 33..33 33 - - - 70900 RMVar_ID_70900 Human_SNP_ID_670334823 m1A Human chr19 + 56087498 56087498 56087498 ACCCGGAATCCAGGAGGGGAAGGAACGACTCGAGCTCTAAGGATGGGACCCGGAAGGCAGAAAAA ACCCGGAATCCAGGAGGGGAAGGAACGACTCGGGCTCTAAGGATGGGACCCGGAAGGCAGAAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56087401..56087550 26863196 MeRIP-seq:(Medium) rs892623712 Functional Loss SNV dbSNP153 33..33 33 - - - 70901 RMVar_ID_70901 Human_SNP_ID_670335474 m1A Human chr19 - 56088033 56088033 56088033 GGGCGGGCGGTGCCCCGAGTGCCGCGGTGGGGAGGGCCGGTAGGGGAGGGGCCCGGGGGGGGGGG GGGCGGGCGGTGCCCCGAGTGCCGCGGTGGGGGGGGCCGGTAGGGGAGGGGCCCGGGGGGGGGGG T C ZNF787 Ensembl:ENSG00000142409 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:56087985..56088194 26863196 MeRIP-seq:(Medium) rs1450373227 Functional Loss SNV dbSNP153 33..33 33 - - - 70902 RMVar_ID_70902 Human_SNP_ID_670335475 m1A Human chr19 - 56088033 56088033 56088033 GGGCGGGCGGTGCCCCGAGTGCCGCGGTGGGGAGGGCCGGTAGGGGAGGGGCCCGGGGGGGGGGG GGGCGGGCGGTGCCCCGAGTGCCGCGGTGGGGCGGGCCGGTAGGGGAGGGGCCCGGGGGGGGGGG T G ZNF787 Ensembl:ENSG00000142409 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:56087985..56088194 26863196 MeRIP-seq:(Medium) rs1450373227 Functional Loss SNV dbSNP153 33..33 33 - - - 70903 RMVar_ID_70903 Human_SNP_ID_670335541 m1A Human chr19 - 56088078 56088078 56088078 CTACCGCGCGGGCGGGGAGGAGGAGGACGACGACGACGAGGCCGCGGGCGGGCGGTGCCCCGAGT CTACCGCGCGGGCGGGGAGGAGGAGGACGACGCCGACGAGGCCGCGGGCGGGCGGTGCCCCGAGT T G ZNF787 Ensembl:ENSG00000142409 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56087648..56101708 26863196 MeRIP-seq:(Medium) rs951263034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146460,Human_RBP_ID_5238914,Human_RBP_ID_6785035,Human_RBP_ID_18192523 70904 RMVar_ID_70904 Human_SNP_ID_670337493 m1A Human chr19 + 56093152 56093119 56093153 TGGGATATTCCATAGACACAGGGGATGGCGGAACTGGGATATTCCATAGACACGGGGATGGCGGA __________________________________TGGGATATTCCATAGACACGGGGATGGCGGA GTGGGATATTCCATAGACACAGGGGATGGCGGAAC G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:56093139..56093265 26863196 MeRIP-seq:(Medium) rs1568524172 Functional Loss DEL dbSNP153 1..34 33 - - - 70905 RMVar_ID_70905 Human_SNP_ID_670341724 m1A Human chr19 - 56105826 56105822 56105826 CGCGCGGGCTTTTTGGAGTTGTTGTAAAGTTGATTGTGGTGAGGGTCGCAAAACTGAATACACTA CGCGCGGGCTTTTTGGAGTTGTTGTAAAGTTG____TGGTGAGGGTCGCAAAACTGAATACACTA ACAAT A ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:56105824..56106227 26863196 MeRIP-seq:(Medium) rs780811502 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_1067321,Human_RBP_ID_17132059,Human_RBP_ID_18493019,Human_RBP_ID_22699167 70906 RMVar_ID_70906 Human_SNP_ID_670342554 m1A Human chr19 + 56107876 56107875 56107877 CGCTCGAAGGCCGGGCATGCTGGGGGCTGCGGAAGAGAGAGCTTGAAGGCCGGGCATGCTGGGGG CGCTCGAAGGCCGGGCATGCTGGGGGCTGCGG__GAGAGAGCTTGAAGGCCGGGCATGCTGGGGG GAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56107874..56107945 26863196 MeRIP-seq:(Medium) rs1216643018 Functional Loss DEL dbSNP153 33..34 33 - - - 70907 RMVar_ID_70907 Human_SNP_ID_670342555 m1A Human chr19 + 56107876 56107876 56107876 CGCTCGAAGGCCGGGCATGCTGGGGGCTGCGGAAGAGAGAGCTTGAAGGCCGGGCATGCTGGGGG CGCTCGAAGGCCGGGCATGCTGGGGGCTGCGGGAGAGAGAGCTTGAAGGCCGGGCATGCTGGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56107874..56107945 26863196 MeRIP-seq:(Medium) rs533267448 Functional Loss SNV dbSNP153 33..33 33 - - - 70908 RMVar_ID_70908 Human_SNP_ID_670342760 m1A Human chr19 - 56108421 56108421 56108421 GGGAGGACTGGAGGAGAGCTCTGGGCAGGGGCAGGGTGGAGGGAGCTGGGGAGCTCTGGGCAGGG GGGAGGACTGGAGGAGAGCTCTGGGCAGGGGCTGGGTGGAGGGAGCTGGGGAGCTCTGGGCAGGG T A ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:56108419..56108600 26863196 MeRIP-seq:(Medium) rs1046280414 Functional Loss SNV dbSNP153 33..33 33 - - - 70909 RMVar_ID_70909 Human_SNP_ID_670342761 m1A Human chr19 - 56108421 56108421 56108421 GGGAGGACTGGAGGAGAGCTCTGGGCAGGGGCAGGGTGGAGGGAGCTGGGGAGCTCTGGGCAGGG GGGAGGACTGGAGGAGAGCTCTGGGCAGGGGCGGGGTGGAGGGAGCTGGGGAGCTCTGGGCAGGG T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:56108419..56108600 26863196 MeRIP-seq:(Medium) rs1046280414 Functional Loss SNV dbSNP153 33..33 33 - - - 70910 RMVar_ID_70910 Human_SNP_ID_670342764 m1A Human chr19 - 56108427 56108427 56108427 GCAGCTGGGAGGACTGGAGGAGAGCTCTGGGCAGGGGCAGGGTGGAGGGAGCTGGGGAGCTCTGG GCAGCTGGGAGGACTGGAGGAGAGCTCTGGGCGGGGGCAGGGTGGAGGGAGCTGGGGAGCTCTGG T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56108425..56108597 26863196 MeRIP-seq:(Medium) rs904994362 Functional Loss SNV dbSNP153 33..33 33 - - - 70911 RMVar_ID_70911 Human_SNP_ID_670342940 m1A Human chr19 + 56109016 56109016 56109016 ACCGGGAGGAACTCAAGAGACCCACGCCGGGGAGGTGGGTGGAGTCACCCCTCCTCCACGGGAGC ACCGGGAGGAACTCAAGAGACCCACGCCGGGGGGGTGGGTGGAGTCACCCCTCCTCCACGGGAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56109009..56109109 32194978 MeRIP-seq:(Medium) rs768015098 Functional Loss SNV dbSNP153 33..33 33 - - - 70912 RMVar_ID_70912 Human_SNP_ID_670343956 m1A Human chr19 - 56112290 56112290 56112290 CTGAGAAACGGAGGCTGGTAAGGGAGGCCGGGACCCTCGTTTCAGAAGATGTGCAATTCCCAGCT CTGAGAAACGGAGGCTGGTAAGGGAGGCCGGGGCCCTCGTTTCAGAAGATGTGCAATTCCCAGCT T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:56112288..56112831 26863196 MeRIP-seq:(Medium) rs563183307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3584109 70913 RMVar_ID_70913 Human_SNP_ID_670344026 m1A Human chr19 + 56112519 56112519 56112519 GTCCCGCCCACCCCTCTGGAGGCCTGCCTGCCAATTATCCCCTTTCTTCTGCTGCCAATCTCACC GTCCCGCCCACCCCTCTGGAGGCCTGCCTGCCGATTATCCCCTTTCTTCTGCTGCCAATCTCACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:56112515..56112788 26863196 MeRIP-seq:(Medium) rs903670292 Functional Loss SNV dbSNP153 33..33 33 - - - 70914 RMVar_ID_70914 Human_SNP_ID_670344740 m1A Human chr19 - 56114796 56114796 56114796 TTGGTTCCGGAAGCAGCCATGGGTACCAGGGCAGCAGGTGCTGGACACCCCTGGCACCTGCCCTC TTGGTTCCGGAAGCAGCCATGGGTACCAGGGCTGCAGGTGCTGGACACCCCTGGCACCTGCCCTC T A ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56114792..56115048 26863196 MeRIP-seq:(Medium) rs990526128 Functional Loss SNV dbSNP153 33..33 33 - - - 70915 RMVar_ID_70915 Human_SNP_ID_670344763 m1A Human chr19 + 56114896 56114896 56114896 GCTCACCTTCCCGCTCTGCTCCCAGCTCAAGAAGCCCACAGCGCCACCCCTCCACTCCCCCACCA GCTCACCTTCCCGCTCTGCTCCCAGCTCAAGAGGCCCACAGCGCCACCCCTCCACTCCCCCACCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56114894..56115030 26863196 MeRIP-seq:(Medium) rs566947359 Functional Loss SNV dbSNP153 33..33 33 - - - 70916 RMVar_ID_70916 Human_SNP_ID_670345074 m1A Human chr19 - 56115757 56115757 56115757 AGATGAAGTCCCTCTCTCTCGCCCTCTCGGAAAGTAGTTGAGTGTGGTGGCTGGGGCCGTGAGCT AGATGAAGTCCCTCTCTCTCGCCCTCTCGGAAGGTAGTTGAGTGTGGTGGCTGGGGCCGTGAGCT T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56115753..56115854 32194978 MeRIP-seq:(Medium) rs750404706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13514161 70917 RMVar_ID_70917 Human_SNP_ID_670346200 m1A Human chr19 - 56119807 56119807 56119807 CGCTGCTGACATTCACCTGCCTGCCTCTGCGCAGTCCCTGTGGTCCTCCGGCCACGCACGGCCTC CGCTGCTGACATTCACCTGCCTGCCTCTGCGCTGTCCCTGTGGTCCTCCGGCCACGCACGGCCTC T A ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56119803..56120041 32194978 MeRIP-seq:(Medium) rs1380912021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3584119,Human_RBP_ID_8100880,Human_RBP_ID_18491045 70918 RMVar_ID_70918 Human_SNP_ID_670346440 m1A Human chr19 - 56120566 56120566 56120566 TGCCCCGGGCGGGCTGCGCGTGGCCTTTGATCAGGCGGGTAATTACGGGGATTCTGGCCGGCAGG TGCCCCGGGCGGGCTGCGCGTGGCCTTTGATCGGGCGGGTAATTACGGGGATTCTGGCCGGCAGG T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:56120550..56120677 26863196 MeRIP-seq:(Medium) rs1051420613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581705,Human_RBP_ID_5377515,Human_RBP_ID_18493044,Human_RBP_ID_18946035 70919 RMVar_ID_70919 Human_SNP_ID_670346579 m1A Human chr19 - 56120916 56120916 56120916 CCGGGCGGCCCGCGGGCGGCGAGCGGGGCTGGAGGGGGGGTGCGCGTGCGCGGGTCCGGGTCCAG CCGGGCGGCCCGCGGGCGGCGAGCGGGGCTGGGGGGGGGGTGCGCGTGCGCGGGTCCGGGTCCAG T C ZNF787 Ensembl:ENSG00000142409 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56120913..56121070 26863196 MeRIP-seq:(Medium) rs967827356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264145,Human_RBP_ID_3581707,Human_RBP_ID_5320606,Human_RBP_ID_8196977,Human_RBP_ID_8728447,Human_RBP_ID_9347044,Human_RBP_ID_18462033,Human_RBP_ID_18946038,Human_RBP_ID_22416938,Human_RBP_ID_22592636,Human_RBP_ID_22720222,Human_RBP_ID_22742051,Human_RBP_ID_26783884 70920 RMVar_ID_70920 Human_SNP_ID_670352295 m1A Human chr19 - 56141354 56141354 56141354 AATCCCTCCCTCCTTCCCCCCTCGCTCACCTCACTCTCTCAGGCGAGGCCCCCCAAGCCCCCTCA AATCCCTCCCTCCTTCCCCCCTCGCTCACCTCGCTCTCTCAGGCGAGGCCCCCCAAGCCCCCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56141209..56142277 26863196 MeRIP-seq:(Medium) rs1186289389 Functional Loss SNV dbSNP153 33..33 33 - - - 70921 RMVar_ID_70921 Human_SNP_ID_670353812 m1A Human chr19 + 56147084 56147084 56147084 CTGGCTGCGGCCCGAGGTGCACACCAAGGAGCAGATGTTGGAGCTGCTGGTGCTGGAACAGTTCC CTGGCTGCGGCCCGAGGTGCACACCAAGGAGCGGATGTTGGAGCTGCTGGTGCTGGAACAGTTCC A G ZNF444 Ensembl:ENSG00000167685 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56147034..56147152 26863196 MeRIP-seq:(Medium) rs1293866548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22977944 Human_miRNA_ID_2301762,Human_miRNA_ID_2305024,Human_miRNA_ID_2308290 RMVar_hsa_circ_118034,RMVar_hsa_circ_196372,RMVar_hsa_circ_275705,RMVar_hsa_circ_196373 70922 RMVar_ID_70922 Human_SNP_ID_670357096 m1A Human chr19 + 56158574 56158574 56158574 GATGTGACGCAGGGCCCTGGGGCCACAGGTGGAAAGGAGGACAGTGGGATGATTCCCTTAGGTGA GATGTGACGCAGGGCCCTGGGGCCACAGGTGGCAAGGAGGACAGTGGGATGATTCCCTTAGGTGA A C ZNF444 Ensembl:ENSG00000167685 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56158523..56160294 32194978 MeRIP-seq:(Medium) rs138226612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912044,Human_RBP_ID_8494330,Human_RBP_ID_8837316,Human_RBP_ID_18998852,Human_RBP_ID_26760231 Human_Splice_Rec_2048444,Human_Splice_Rec_2048445,Human_Splice_Rec_2048454,Human_Splice_Rec_2048455,Human_Splice_Rec_2048462,Human_Splice_Rec_2048463,Human_Splice_Rec_2048475,Human_Splice_Rec_2048478,Human_Splice_Rec_2048479 RMVar_hsa_circ_118034,RMVar_hsa_circ_113831,RMVar_hsa_circ_196373,RMVar_hsa_circ_196374 70923 RMVar_ID_70923 Human_SNP_ID_670357641 m1A Human chr19 + 56159873 56159873 56159873 CTGCCCTGAGTGCGGGAAGGCCTTTCGGCGCAAGGAGCACCTGCGGCGCCACCGCGACACGCACC CTGCCCTGAGTGCGGGAAGGCCTTTCGGCGCAGGGAGCACCTGCGGCGCCACCGCGACACGCACC A G ZNF444 Ensembl:ENSG00000167685 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:56159823..56159920 26863196 MeRIP-seq:(Medium) rs769145306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1018179 RMVar_hsa_circ_118034,RMVar_hsa_circ_113831,RMVar_hsa_circ_196373,RMVar_hsa_circ_196374 70924 RMVar_ID_70924 Human_SNP_ID_670357642 m1A Human chr19 + 56159873 56159873 56159873 CTGCCCTGAGTGCGGGAAGGCCTTTCGGCGCAAGGAGCACCTGCGGCGCCACCGCGACACGCACC CTGCCCTGAGTGCGGGAAGGCCTTTCGGCGCATGGAGCACCTGCGGCGCCACCGCGACACGCACC A T ZNF444 Ensembl:ENSG00000167685 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:56159823..56159920 26863196 MeRIP-seq:(Medium) rs769145306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1018179 RMVar_hsa_circ_118034,RMVar_hsa_circ_113831,RMVar_hsa_circ_196373,RMVar_hsa_circ_196374 70925 RMVar_ID_70925 Human_SNP_ID_670357842 m1A Human chr19 + 56160215 56160215 56160215 GCCCTGGCCCTTGGGTTAGCCGCCTCCCGGCCAGCGCCATCTCCCGCCCTTGGTGCTGCCCCCGG GCCCTGGCCCTTGGGTTAGCCGCCTCCCGGCCTGCGCCATCTCCCGCCCTTGGTGCTGCCCCCGG A T ZNF444 Ensembl:ENSG00000167685 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56160168..56160834 26863196 MeRIP-seq:(Medium) rs1412822969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527335 RMVar_hsa_circ_118034,RMVar_hsa_circ_113831,RMVar_hsa_circ_196373,RMVar_hsa_circ_196374 70926 RMVar_ID_70926 Human_SNP_ID_670392679 m1A Human chr19 - 56273884 56273884 56273884 GAGGGCAAGACACATTGTTTAAACACACAGAAACACACATACATGCACACACACGCTCCTAAATA GAGGGCAAGACACATTGTTTAAACACACAGAAGCACACATACATGCACACACACGCTCCTAAATA T C ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:56273842..56273969 26863196 MeRIP-seq:(Medium) rs1013433907 Functional Loss SNV dbSNP153 33..33 33 - - - 70927 RMVar_ID_70927 Human_SNP_ID_670397530 m1A Human chr19 - 56294092 56294092 56294092 GTGTTTGGGATTTTCCTGCTGGGTCTGCTTTCAGTTTGCAAAGTGCTGTCAGTGCAGCATGAGGA GTGTTTGGGATTTTCCTGCTGGGTCTGCTTTCGGTTTGCAAAGTGCTGTCAGTGCAGCATGAGGA T C ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56294075..56294175 32194978 MeRIP-seq:(Medium) rs1192414843 Functional Loss SNV dbSNP153 33..33 33 - - - 70928 RMVar_ID_70928 Human_SNP_ID_670397974 m1A Human chr19 - 56295857 56295857 56295857 GAGTATGGAGTTCCCAGGAGCCGTGGAAGAGGAGGCCACATGTAGGGAAAAATCACAACATCAGA GAGTATGGAGTTCCCAGGAGCCGTGGAAGAGGTGGCCACATGTAGGGAAAAATCACAACATCAGA T A ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:56295743..56295884 26863196 MeRIP-seq:(Medium) rs1325999514 Functional Loss SNV dbSNP153 33..33 33 - - - 70929 RMVar_ID_70929 Human_SNP_ID_670398337 m1A Human chr19 - 56297350 56297348 56297351 GGGAGGGAGGAAGAGGAAGAGGAGGAGAAAAGAAAGGAAAAGAAAAGAAACCATCAGGTGAATTA GGGAGGGAGGAAGAGGAAGAGGAGGAGAAAA___AGGAAAAGAAAAGAAACCATCAGGTGAATTA TTTC T ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56297348..56297413 26863196 MeRIP-seq:(Medium) rs377278275 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22976326,Human_RBP_ID_25448194 70930 RMVar_ID_70930 Human_SNP_ID_670399706 m1A Human chr19 - 56302475 56302475 56302475 AGGGCAGAGAGGGAAGAAGGATGGGAAGGAAGAAGGGAGGGAGGAAGCAGACGGAGAGAGGAAGA AGGGCAGAGAGGGAAGAAGGATGGGAAGGAAGGAGGGAGGGAGGAAGCAGACGGAGAGAGGAAGA T C ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:56302449..56302518 26863196 MeRIP-seq:(Medium) rs1195097322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196986,Human_RBP_ID_17068458 70931 RMVar_ID_70931 Human_SNP_ID_670402897 m1A Human chr19 + 56314786 56314786 56314786 AAACGAGTCAGGCATCGTGGTAGGACCTGGCGAGTGGGGCCGGGGAGAGCGGGACGCCTGGATCG AAACGAGTCAGGCATCGTGGTAGGACCTGGCGGGTGGGGCCGGGGAGAGCGGGACGCCTGGATCG A G AC006116.9 Ensembl:ENSG00000267549 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:56314735..56314806 26863196 MeRIP-seq:(Medium) rs1179023653 Functional Loss SNV dbSNP153 33..33 33 - - - 70932 RMVar_ID_70932 Human_SNP_ID_670477725 m1A Human chr19 - 56622651 56622567 56622651 AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGCACAGTGAGGGAGGAGTTCTTGATGAAGGACTTC AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGC_________________________________ AGCACCAGCGGATCCACACCGGCGAGAAGCCGTACAGGTGCGGCCAGTGCGGGAAGTCCTTCATCAAGAACTCCTCCCTCACTGT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56622600..56622750 32194978 MeRIP-seq:(Medium) rs1568510458 Functional Loss DEL dbSNP153 33..65 33 - - - 70933 RMVar_ID_70933 Human_SNP_ID_670477776 m1A Human chr19 - 56622651 56622651 56622651 AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGCACAGTGAGGGAGGAGTTCTTGATGAAGGACTTC AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGCTCAGTGAGGGAGGAGTTCTTGATGAAGGACTTC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56622600..56622750 32194978 MeRIP-seq:(Medium) rs765397884 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 70934 RMVar_ID_70934 Human_SNP_ID_670477777 m1A Human chr19 - 56622651 56622651 56622651 AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGCACAGTGAGGGAGGAGTTCTTGATGAAGGACTTC AGGGCTTCTCGCCCGTGTGGATCCGCTGGTGCGCAGTGAGGGAGGAGTTCTTGATGAAGGACTTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:56622600..56622750 32194978 MeRIP-seq:(Medium) rs765397884 Functional Loss SNV dbSNP153 33..33 33 - - - 70935 RMVar_ID_70935 Human_SNP_ID_670636471 m1A Human chr19 + 57191594 57191594 57191594 TTTGCAGGTCCCTAGTCAGGACCGAGCAGGGGAGTAGGATAGGAATCCCCGCCGCACCTTTGTAC TTTGCAGGTCCCTAGTCAGGACCGAGCAGGGGCGTAGGATAGGAATCCCCGCCGCACCTTTGTAC A C ZNF264 Ensembl:ENSG00000083844 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57191548..57191676 26863196 MeRIP-seq:(Medium) rs935800692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6786315,Human_RBP_ID_13516890 70936 RMVar_ID_70936 Human_SNP_ID_670636472 m1A Human chr19 + 57191594 57191594 57191594 TTTGCAGGTCCCTAGTCAGGACCGAGCAGGGGAGTAGGATAGGAATCCCCGCCGCACCTTTGTAC TTTGCAGGTCCCTAGTCAGGACCGAGCAGGGGTGTAGGATAGGAATCCCCGCCGCACCTTTGTAC A T ZNF264 Ensembl:ENSG00000083844 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57191548..57191676 26863196 MeRIP-seq:(Medium) rs935800692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6786315,Human_RBP_ID_13516890 70937 RMVar_ID_70937 Human_SNP_ID_670660472 m1A Human chr19 - 57280545 57280545 57280545 AAGACGCGAAGAAGGGGCGTAACCGCTTCACTACCCGTCCCTGCTCAGGCCGCAGAACGCGCCCA AAGACGCGAAGAAGGGGCGTAACCGCTTCACTGCCCGTCCCTGCTCAGGCCGCAGAACGCGCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57280494..57280664 26863196 MeRIP-seq:(Medium) rs1410525656 Functional Loss SNV dbSNP153 33..33 33 - - - 70938 RMVar_ID_70938 Human_SNP_ID_670660483 m1A Human chr19 - 57280577 57280577 57280577 TTAGGGGAGAAGCGGGGCGTCAGGCTCCCGCCAAGACGCGAAGAAGGGGCGTAACCGCTTCACTA TTAGGGGAGAAGCGGGGCGTCAGGCTCCCGCCCAGACGCGAAGAAGGGGCGTAACCGCTTCACTA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:57280526..57280700 26863196 MeRIP-seq:(Medium) rs1263770470 Functional Loss SNV dbSNP153 33..33 33 - - - 70939 RMVar_ID_70939 Human_SNP_ID_670660486 m1A Human chr19 + 57280584 57280584 57280584 GCGGTTACGCCCCTTCTTCGCGTCTTGGCGGGAGCCTGACGCCCCGCTTCTCCCCTAACGAGGTG GCGGTTACGCCCCTTCTTCGCGTCTTGGCGGGGGCCTGACGCCCCGCTTCTCCCCTAACGAGGTG A G ZNF460 Ensembl:ENSG00000197714 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:57280536..57280665 26863196 MeRIP-seq:(Medium) rs928538586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240796,Human_RBP_ID_914644,Human_RBP_ID_4557735,Human_RBP_ID_5443494,Human_RBP_ID_8840252 Human_miRNA_ID_3066434 RMVar_hsa_circ_196399,RMVar_hsa_circ_87432,RMVar_hsa_circ_196400 70940 RMVar_ID_70940 Human_SNP_ID_670671392 m1A Human chr19 + 57320571 57320571 57320571 GGCGCGTCCAGCGGCCTGAGCAGGGGAGGGTAATGAGGCTGTTACGCGCCTTCTCCGCATCTTGG GGCGCGTCCAGCGGCCTGAGCAGGGGAGGGTAGTGAGGCTGTTACGCGCCTTCTCCGCATCTTGG A G ZNF543 Ensembl:ENSG00000178229 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57320523..57320590 26863196 MeRIP-seq:(Medium) rs1292335593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527950,Human_RBP_ID_4559936,Human_RBP_ID_18420991,Human_RBP_ID_23808825 RMVar_hsa_circ_196399 70941 RMVar_ID_70941 Human_SNP_ID_670671418 m1A Human chr19 - 57320654 57320654 57320654 CGGAGGGCGGCTGCGGAGGCCTAGGCCTCGGCAGGCGCCGGTGGAACACCCCGTTAGGGAAGAAG CGGAGGGCGGCTGCGGAGGCCTAGGCCTCGGCTGGCGCCGGTGGAACACCCCGTTAGGGAAGAAG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:57320603..57320735 26863196 MeRIP-seq:(Medium) rs1264501887 Functional Loss SNV dbSNP153 33..33 33 - - - 70942 RMVar_ID_70942 Human_SNP_ID_670671419 m1A Human chr19 - 57320654 57320654 57320654 CGGAGGGCGGCTGCGGAGGCCTAGGCCTCGGCAGGCGCCGGTGGAACACCCCGTTAGGGAAGAAG CGGAGGGCGGCTGCGGAGGCCTAGGCCTCGGCGGGCGCCGGTGGAACACCCCGTTAGGGAAGAAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:57320603..57320735 26863196 MeRIP-seq:(Medium) rs1264501887 Functional Loss SNV dbSNP153 33..33 33 - - - 70943 RMVar_ID_70943 Human_SNP_ID_670680419 m1A Human chr19 + 57353628 57353628 57353628 TATCTCCTCTTAGTTGGGAGGCTGGGGAGGCGAGGGACTAGAGAGTGGGTGTGTGAGTGTGTAGA TATCTCCTCTTAGTTGGGAGGCTGGGGAGGCGGGGGACTAGAGAGTGGGTGTGTGAGTGTGTAGA A G ZNF304 Ensembl:ENSG00000131845 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:57353582..57353702 26863196 MeRIP-seq:(Medium) rs1179150575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823764,Human_RBP_ID_9427767 70944 RMVar_ID_70944 Human_SNP_ID_670683165 m1A Human chr19 + 57363574 57363574 57363574 TGGTTCCTTGTACGCAGAGGCGGTAGTGACACAGGCACAACTGACAGTGGCAGAAGCTCAGCTGA TGGTTCCTTGTACGCAGAGGCGGTAGTGACACGGGCACAACTGACAGTGGCAGAAGCTCAGCTGA A G TRAPPC2B,AC003002.1,ZNF547 Ensembl:ENSG00000256060,Ensembl:ENSG00000268133,Ensembl:ENSG00000152433 Protein coding,Protein coding,Protein coding 5'UTR,5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:57363526..57363675 26863196 MeRIP-seq:(Medium) rs558502943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5421897,Human_RBP_ID_5500245,Human_RBP_ID_13519041,Human_RBP_ID_17932095,Human_RBP_ID_27471824 70945 RMVar_ID_70945 Human_SNP_ID_670683620 m1A Human chr19 - 57364860 57364860 57364860 ATTTCAAAAACTGGATTATCATGGTGACCAACAATTACAAAGTAGAAGCTTCCAGACATGGTCTT ATTTCAAAAACTGGATTATCATGGTGACCAACCATTACAAAGTAGAAGCTTCCAGACATGGTCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57364775..57364875 26863196 MeRIP-seq:(Medium) rs1465432667 Functional Loss SNV dbSNP153 33..33 33 - - - 70946 RMVar_ID_70946 Human_SNP_ID_670690405 m1A Human chr19 - 57390465 57390465 57390465 TGTCCATTCCTAACCTGGTTTTCCTAACTTGAAACTTCGAACTCTGGACCTGCCCCCTCCAACTG TGTCCATTCCTAACCTGGTTTTCCTAACTTGATACTTCGAACTCTGGACCTGCCCCCTCCAACTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57390455..57390528 26863196 MeRIP-seq:(Medium) rs528797537 Functional Loss SNV dbSNP153 33..33 33 - - - 70947 RMVar_ID_70947 Human_SNP_ID_670691798 m1A Human chr19 - 57396108 57396108 57396108 TCACACCTCCACTCCAGTCAATTCCACAGACAACTCCCAGCCCACACCACAGGCATTTCCTTCAC TCACACCTCCACTCCAGTCAATTCCACAGACACCTCCCAGCCCACACCACAGGCATTTCCTTCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57396060..57396134 26863196 MeRIP-seq:(Medium) rs145180289 Functional Loss SNV dbSNP153 33..33 33 - - - 70948 RMVar_ID_70948 Human_SNP_ID_670695983 m1A Human chr19 - 57412450 57412447 57412451 ATGGAGCGAGACTCTGTCTCAAAAAAAAAAAAAATGTTTTACACATTCATAAATAAATAAGTTGC ATGGAGCGAGACTCTGTCTCAAAAAAAAAAA____GTTTTACACATTCATAAATAAATAAGTTGC CATTT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:57412419..57412546 26863196 MeRIP-seq:(Medium) rs1006670124 Functional Loss DEL dbSNP153 32..35 33 - - - 70949 RMVar_ID_70949 Human_SNP_ID_670695991 m1A Human chr19 - 57412450 57412448 57412450 ATGGAGCGAGACTCTGTCTCAAAAAAAAAAAAAATGTTTTACACATTCATAAATAAATAAGTTGC ATGGAGCGAGACTCTGTCTCAAAAAAAAAAAA__TGTTTTACACATTCATAAATAAATAAGTTGC ATT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:57412419..57412546 26863196 MeRIP-seq:(Medium) rs34661992 Functional Loss DEL dbSNP153 33..34 33 - - - 70950 RMVar_ID_70950 Human_SNP_ID_670695992 m1A Human chr19 - 57412450 57412448 57412450 ATGGAGCGAGACTCTGTCTCAAAAAAAAAAAAAATGTTTTACACATTCATAAATAAATAAGTTGC ATGGAGCGAGACTCTGTCTCAAAAAAAAAAAA_ATGTTTTACACATTCATAAATAAATAAGTTGC ATT AT - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:57412419..57412546 26863196 MeRIP-seq:(Medium) rs34661992 Functional Loss DEL dbSNP153 33..33 33 - - - 70951 RMVar_ID_70951 Human_SNP_ID_670696919 m1A Human chr19 - 57416094 57416094 57416094 GTTTCTTTCTTTGACCTCAGCTTTCCAAACCCACATATTCTTGCACACCTCCTTTGAGTTCCAGA GTTTCTTTCTTTGACCTCAGCTTTCCAAACCCTCATATTCTTGCACACCTCCTTTGAGTTCCAGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57416046..57416129 26863196 MeRIP-seq:(Medium) rs1475607634 Functional Loss SNV dbSNP153 33..33 33 - - - 70952 RMVar_ID_70952 Human_SNP_ID_670702015 m1A Human chr19 + 57435923 57435923 57435923 CCATAGAGGGCTGTGCAGGGAGGACGAATGGGAGGGTCACGCCCAGAGTTAGAAGTTTAAAGTTG CCATAGAGGGCTGTGCAGGGAGGACGAATGGGGGGGTCACGCCCAGAGTTAGAAGTTTAAAGTTG A G ZNF749,AC003002.2 Ensembl:ENSG00000186230,Ensembl:ENSG00000268533 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57435919..57436040 26863196 MeRIP-seq:(Medium) rs1042812504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8233232 RMVar_hsa_circ_80511,RMVar_hsa_circ_196413,RMVar_hsa_circ_196415 70953 RMVar_ID_70953 Human_SNP_ID_670716239 m1A Human chr19 + 57487814 57487814 57487814 CTGCGAGAAGCTGGTTGTGCGCTGAGGCGACCAGCGCCGGAAGGCACGGTGGCGACTCACGCTGT CTGCGAGAAGCTGGTTGTGCGCTGAGGCGACCGGCGCCGGAAGGCACGGTGGCGACTCACGCTGT A G ZNF419,AC003005.1 Ensembl:ENSG00000105136,Ensembl:ENSG00000268107 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57487763..57487946 26863196 MeRIP-seq:(Medium) rs8113039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18740467 70954 RMVar_ID_70954 Human_SNP_ID_670734964 m1A Human chr19 + 57556354 57556354 57556354 AAAGGTCACAGCCACATCCTTGAAGGTCACCAACATCTGGAAAGTCAAACAGAAGTAATGCTATT AAAGGTCACAGCCACATCCTTGAAGGTCACCAGCATCTGGAAAGTCAAACAGAAGTAATGCTATT A G ZNF549 Ensembl:ENSG00000121406 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:57556337..57556414 26863196 MeRIP-seq:(Medium) rs1431737242 Functional Loss SNV dbSNP153 33..33 33 - - - 70955 RMVar_ID_70955 Human_SNP_ID_670735820 m1A Human chr19 - 57559781 57559781 57559781 CGCGCTCTCAGAACTGTGCTGGGAAGGATGGTAGGGCGACTGGGGCTCACCTCCGCACCGTTGTA CGCGCTCTCAGAACTGTGCTGGGAAGGATGGTGGGGCGACTGGGGCTCACCTCCGCACCGTTGTA T C ZNF550 Ensembl:ENSG00000251369 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:57559669..57559816;chr19:57559611..57559826 26863196 MeRIP-seq:(Medium) rs368943301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242021,Human_RBP_ID_4550324,Human_RBP_ID_5527182,Human_RBP_ID_9383007,Human_RBP_ID_18420994 70956 RMVar_ID_70956 Human_SNP_ID_670739776 m1A Human chr19 + 57576652 57576652 57576652 CTAGCGCTGCACTTGATGTCCTCTCTTAAGTCACAGCCTTCCTCTCCTGCTAACCCTCATTCAAA CTAGCGCTGCACTTGATGTCCTCTCTTAAGTCGCAGCCTTCCTCTCCTGCTAACCCTCATTCAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57576613..57576711 26863196 MeRIP-seq:(Medium) rs1224598618 Functional Loss SNV dbSNP153 33..33 33 - - - 70957 RMVar_ID_70957 Human_SNP_ID_670739819 m1A Human chr19 + 57576903 57576903 57576903 CCAAGCATTGATCTCATGCCCACTCTTCTCCTAGATCCTTGGCCACTTGCCAGATCATCCTTGCT CCAAGCATTGATCTCATGCCCACTCTTCTCCTGGATCCTTGGCCACTTGCCAGATCATCCTTGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57576852..57576959 26863196 MeRIP-seq:(Medium) rs563800616 Functional Loss SNV dbSNP153 33..33 33 - - - 70958 RMVar_ID_70958 Human_SNP_ID_670739821 m1A Human chr19 - 57576909 57576909 57576909 TGTGAGAGCAAGGATGATCTGGCAAGTGGCCAAGGATCTAGGAGAAGAGTGGGCATGAGATCAAT TGTGAGAGCAAGGATGATCTGGCAAGTGGCCAGGGATCTAGGAGAAGAGTGGGCATGAGATCAAT T C ZNF416 Ensembl:ENSG00000083817 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57576873..57576954 26863196 MeRIP-seq:(Medium) rs1457872565 Functional Loss SNV dbSNP153 33..33 33 - - - 70959 RMVar_ID_70959 Human_SNP_ID_670746188 m1A Human chr19 - 57602499 57602493 57602499 CTCCCACCCTTCCCCTTCCTGGCCTGCTATTAATATTATCATCATGACCAGGAATCCCACTACTA CTCCCACCCTTCCCCTTCCTGGCCTGCTATTA______TCATCATGACCAGGAATCCCACTACTA ATAATAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57602454..57602753 26863196 MeRIP-seq:(Medium) rs1298045615 Functional Loss DEL dbSNP153 33..38 33 - - - 70960 RMVar_ID_70960 Human_SNP_ID_670749314 m1A Human chr19 + 57614322 57614322 57614322 TCGGGGTTGCTGGGCGGTTCCGAGGTGACGGAAGCGGGAGGGTGCGGGAGAAGTCGCTGTTCGCT TCGGGGTTGCTGGGCGGTTCCGAGGTGACGGAGGCGGGAGGGTGCGGGAGAAGTCGCTGTTCGCT A G ZNF134 Ensembl:ENSG00000213762 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57614274..57614444 26863196 MeRIP-seq:(Medium) rs1448682722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240995,Human_RBP_ID_773033,Human_RBP_ID_9383008,Human_RBP_ID_18420995 70961 RMVar_ID_70961 Human_SNP_ID_670783686 m1A Human chr19 - 57746925 57746925 57746925 GCCTTTAAGGAGCTGCAGAGCAGCCTCTGTGCAGTCGGGACAACGTCTCGTCTCCACCTTCTGGG GCCTTTAAGGAGCTGCAGAGCAGCCTCTGTGCCGTCGGGACAACGTCTCGTCTCCACCTTCTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:57746877..57747044 26863196 MeRIP-seq:(Medium) rs1299416822 Functional Loss SNV dbSNP153 33..33 33 - - - 70962 RMVar_ID_70962 Human_SNP_ID_670790266 m1A Human chr19 + 57771646 57771646 57771646 TTACTTAGAAGTGAAACTAGAGGGGTGAGGTGATGTTACCAATTTCTTAATAGGCGCTGTCTGGT TTACTTAGAAGTGAAACTAGAGGGGTGAGGTGGTGTTACCAATTTCTTAATAGGCGCTGTCTGGT A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57771641..57771729 26863196 MeRIP-seq:(Medium) rs1394024405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23809445 RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_196447,RMVar_hsa_circ_103002,RMVar_hsa_circ_119754,RMVar_hsa_circ_196448 70963 RMVar_ID_70963 Human_SNP_ID_670798797 m1A Human chr19 - 57803542 57803542 57803542 AGTCCGGAGAAGAAAGGGAAACGGGATGAGAGAGCGGAAAATAGAGTGCAAATGAGAGAAAGAAA AGTCCGGAGAAGAAAGGGAAACGGGATGAGAGGGCGGAAAATAGAGTGCAAATGAGAGAAAGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57803371..57803693 26863196 MeRIP-seq:(Medium) rs963850810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17068594 70964 RMVar_ID_70964 Human_SNP_ID_670798800 m1A Human chr19 - 57803560 57803560 57803560 TGCGGCAGGAGCGGGAGAAGTCCGGAGAAGAAAGGGAAACGGGATGAGAGAGCGGAAAATAGAGT TGCGGCAGGAGCGGGAGAAGTCCGGAGAAGAAGGGGAAACGGGATGAGAGAGCGGAAAATAGAGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:57803363..57803732 26863196 MeRIP-seq:(Medium) rs1216979179 Functional Loss SNV dbSNP153 33..33 33 - - - 70965 RMVar_ID_70965 Human_SNP_ID_670802135 m1A Human chr19 - 57814581 57814581 57814581 ACCCGGCGTCGGGACACTGAGGCGCTCTCGGGAGGGATCCCTGTTTCAGACACCCGTGGGATGCG ACCCGGCGTCGGGACACTGAGGCGCTCTCGGGCGGGATCCCTGTTTCAGACACCCGTGGGATGCG T G ZNF552 Ensembl:ENSG00000178935 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57814562..57814674 26863196 MeRIP-seq:(Medium) rs753880935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2050699 70966 RMVar_ID_70966 Human_SNP_ID_670829567 m1A Human chr19 - 57904340 57904340 57904340 CTCAGGGGCCAACGCCAGTATGGAGGCTGCAAAGGCCCTGAGCTCTAGGAGCCCACACTATTTAT CTCAGGGGCCAACGCCAGTATGGAGGCTGCAAGGGCCCTGAGCTCTAGGAGCCCACACTATTTAT T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:57904289..57904450 26863196 MeRIP-seq:(Medium) rs568481872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 70967 RMVar_ID_70967 Human_SNP_ID_670833215 m1A Human chr19 + 57916549 57916549 57916549 TCACCGCGGTCCCCCCCCAGCACTCAGGGGCCACAAACTGGGGAAACACCCGCGTCACCGATACA TCACCGCGGTCCCCCCCCAGCACTCAGGGGCCGCAAACTGGGGAAACACCCGCGTCACCGATACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57916441..57916554 26863196 MeRIP-seq:(Medium) rs1316032975 Functional Loss SNV dbSNP153 33..33 33 - - - 70968 RMVar_ID_70968 Human_SNP_ID_670883919 m1A Human chr19 - 58084968 58084968 58084968 CTTGTCCCGCGGGAAGCCCTATGCCTGCGGCGAGTGCGGGGAGGCCTTCGCGTGGCTCTCGCACC CTTGTCCCGCGGGAAGCCCTATGCCTGCGGCGTGTGCGGGGAGGCCTTCGCGTGGCTCTCGCACC T A ZSCAN18 Ensembl:ENSG00000121413 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58084468..58085529 32194978 MeRIP-seq:(Medium) rs1418866650 Functional Loss SNV dbSNP153 33..33 33 - - - 70969 RMVar_ID_70969 Human_SNP_ID_670884828 m1A Human chr19 + 58087383 58087382 58087384 TTGCTTCTCTGACCCTCCTCTGTTCCAGAAACAGGGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG TTGCTTCTCTGACCCTCCTCTGTTCCAGAAAC__GGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG CAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58087319..58087419 32194978 MeRIP-seq:(Medium) rs762210790 Functional Loss DEL dbSNP153 33..34 33 - - - 70970 RMVar_ID_70970 Human_SNP_ID_670884831 m1A Human chr19 + 58087383 58087383 58087383 TTGCTTCTCTGACCCTCCTCTGTTCCAGAAACAGGGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG TTGCTTCTCTGACCCTCCTCTGTTCCAGAAACCGGGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58087319..58087419 32194978 MeRIP-seq:(Medium) rs553110163 Functional Loss SNV dbSNP153 33..33 33 - - - 70971 RMVar_ID_70971 Human_SNP_ID_670884832 m1A Human chr19 + 58087383 58087383 58087383 TTGCTTCTCTGACCCTCCTCTGTTCCAGAAACAGGGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG TTGCTTCTCTGACCCTCCTCTGTTCCAGAAACGGGGGGTCCGGAGAAAGCCAGGCTGGGGAGAAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58087319..58087419 32194978 MeRIP-seq:(Medium) rs553110163 Functional Loss SNV dbSNP153 33..33 33 - - - 70972 RMVar_ID_70972 Human_SNP_ID_670912055 m1A Human chr19 - 58182695 58182695 58182695 GAGATGGGTCCTGCCTGAAAGTGAGGGTGGACAGGGCCAAGTGTCCACTCAAGGTCAGGGAGGGG GAGATGGGTCCTGCCTGAAAGTGAGGGTGGACGGGGCCAAGTGTCCACTCAAGGTCAGGGAGGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58182644..58182832 26863196 MeRIP-seq:(Medium) rs1461928231 Functional Loss SNV dbSNP153 33..33 33 - - - 70973 RMVar_ID_70973 Human_SNP_ID_670912084 m1A Human chr19 - 58182791 58182788 58182791 CTGAAGTTCCACCAGTTTCAAAGTCGAGAAAGAAGGGGAGGACTGGGAGAGCCGGAAGTGTGCAG CTGAAGTTCCACCAGTTTCAAAGTCGAGAAAG___GGGAGGACTGGGAGAGCCGGAAGTGTGCAG CCTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58182742..58182814 26863196 MeRIP-seq:(Medium) rs1362262451 Functional Loss DEL dbSNP153 33..35 33 - - - 70974 RMVar_ID_70974 Human_SNP_ID_670912280 m1A Human chr19 - 58183346 58183346 58183346 ACTACAACTCCCAGACGCCCCCGCGGCGCGCCAGCTTGCCTCACCCAGCGGCGGCCATCTTGACT ACTACAACTCCCAGACGCCCCCGCGGCGCGCCGGCTTGCCTCACCCAGCGGCGGCCATCTTGACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58183076..58183394 26863196 MeRIP-seq:(Medium) rs1272385962 Functional Loss SNV dbSNP153 33..33 33 - - - 70975 RMVar_ID_70975 Human_SNP_ID_670912729 m1A Human chr19 - 58184740 58184740 58184740 TCTCTGAGCTGCACCATCACACCCAAGCCGTCAGCCCCTACCCAGGGCCCTGATGCTTCTTTCTA TCTCTGAGCTGCACCATCACACCCAAGCCGTCCGCCCCTACCCAGGGCCCTGATGCTTCTTTCTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58184578..58184788 26863196 MeRIP-seq:(Medium) rs1197362213 Functional Loss SNV dbSNP153 33..33 33 - - - 70976 RMVar_ID_70976 Human_SNP_ID_670916890 m1A Human chr19 + 58200446 58200446 58200446 ATATTTGGGATGGTAATGAGTGTTGGAAAGAGAAGGAAACAATGGGATACATTGGTGGGGGACAA ATATTTGGGATGGTAATGAGTGTTGGAAAGAGGAGGAAACAATGGGATACATTGGTGGGGGACAA A G ZNF274 Ensembl:ENSG00000171606 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58200402..58200534 26863196 MeRIP-seq:(Medium) rs1361535496 Functional Loss SNV dbSNP153 33..33 33 - - - 70977 RMVar_ID_70977 Human_SNP_ID_670919231 m1A Human chr19 - 58209530 58209530 58209530 TCCTTCTTCCCTCTCTCCTCCCACCTCATGGAAGGTGAGACTTTCCCTGGACCCATGAAATGCAG TCCTTCTTCCCTCTCTCCTCCCACCTCATGGAGGGTGAGACTTTCCCTGGACCCATGAAATGCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58209516..58209643 26863196 MeRIP-seq:(Medium) rs972643388 Functional Loss SNV dbSNP153 33..33 33 - - - 70978 RMVar_ID_70978 Human_SNP_ID_670924952 m1A Human chr19 + 58230564 58230564 58230564 CAGACAAGGAAGGACAGGGTTAGAGAGCAAAGATGGACACAGGCAGTGAGAGATTCCCCAGGGAA CAGACAAGGAAGGACAGGGTTAGAGAGCAAAGGTGGACACAGGCAGTGAGAGATTCCCCAGGGAA A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58230483..58230601 26863196 MeRIP-seq:(Medium) rs1173308901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6791157 RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 70979 RMVar_ID_70979 Human_SNP_ID_670924991 m1A Human chr19 - 58230745 58230745 58230745 CTTCTCCTCTCAGGTGAGGCCTGAACAGAGTGACCAACACTCTCAGTTTCCCCCTCCTCATCTTG CTTCTCCTCTCAGGTGAGGCCTGAACAGAGTGTCCAACACTCTCAGTTTCCCCCTCCTCATCTTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58230707..58231059 26863196 MeRIP-seq:(Medium) rs578101533 Functional Loss SNV dbSNP153 33..33 33 - - - 70980 RMVar_ID_70980 Human_SNP_ID_670925069 m1A Human chr19 + 58231118 58231117 58231118 GTTGGGCAGAGAGGGCAGTCAAGGGCATAGGCAGATTGCACAGAACAAACAGATCAGAGAGGCCA GTTGGGCAGAGAGGGCAGTCAAGGGCATAGGC_GATTGCACAGAACAAACAGATCAGAGAGGCCA CA C ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58231106..58231201 26863196 MeRIP-seq:(Medium) rs1568732649 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 70981 RMVar_ID_70981 Human_SNP_ID_670928617 m1A Human chr19 + 58244050 58244050 58244050 GAGGAAATGGAAGCACGTTCTATGCTGGTTCCACCCCAGGTGAGTGGGGGGTCTTTGCTCTCAGT GAGGAAATGGAAGCACGTTCTATGCTGGTTCCTCCCCAGGTGAGTGGGGGGTCTTTGCTCTCAGT A T ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58229531..58246301 32194978 MeRIP-seq:(Medium) rs763394810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914713 Human_Splice_Rec_2051368,Human_Splice_Rec_2051369,Human_Splice_Rec_2051386,Human_Splice_Rec_2051387,Human_Splice_Rec_2051398,Human_Splice_Rec_2051399,Human_Splice_Rec_2051410,Human_Splice_Rec_2051411,Human_Splice_Rec_2051424,Human_Splice_Rec_2051425,Human_Splice_Rec_2051440,Human_Splice_Rec_2051441,Human_Splice_Rec_2051468,Human_Splice_Rec_2051469,Human_Splice_Rec_2051478,Human_Splice_Rec_2051479,Human_Splice_Rec_2051486,Human_Splice_Rec_2051487,Human_Splice_Rec_2051494,Human_Splice_Rec_2051495,Human_Splice_Rec_2051504,Human_Splice_Rec_2051505,Human_Splice_Rec_2051514,Human_Splice_Rec_2051515,Human_Splice_Rec_2051527,Human_Splice_Rec_2051533,Human_Splice_Rec_2051546,Human_Splice_Rec_2051547,Human_Splice_Rec_2051564,Human_Splice_Rec_2051565 RMVar_hsa_circ_41224,RMVar_hsa_circ_100464,RMVar_hsa_circ_69347,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493,RMVar_hsa_circ_275450,RMVar_hsa_circ_196494 70982 RMVar_ID_70982 Human_SNP_ID_670932530 m1A Human chr19 - 58258586 58258557 58258587 CCAGCACTCTCACACGTGGTGCCCTCACACCCAGCACCCTCACACCCAGCACCCTCACACCTGGT CCAGCACTCTCACACGTGGTGCCCTCACACC______________________________TGGT AGGTGTGAGGGTGCTGGGTGTGAGGGTGCTG A AC020915.3 Ensembl:ENSG00000268516 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58258336..58258697;chr19:58258325..58258679 26863196 MeRIP-seq:(Medium) rs1176492271 Functional Loss DEL dbSNP153 32..61 33 - - - 70983 RMVar_ID_70983 Human_SNP_ID_670932531 m1A Human chr19 - 58258586 58258557 58258587 CCAGCACTCTCACACGTGGTGCCCTCACACCCAGCACCCTCACACCCAGCACCCTCACACCTGGT CCAGCACTCTCACACGTGGTGCCCTCACACC_______________CAGCACCCTCACACCTGGT AGGTGTGAGGGTGCTGGGTGTGAGGGTGCTG AGGTGTGAGGGTGCTG AC020915.3 Ensembl:ENSG00000268516 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58258336..58258697;chr19:58258325..58258679 26863196 MeRIP-seq:(Medium) rs1176492271 Functional Loss DEL dbSNP153 32..46 33 - - - 70984 RMVar_ID_70984 Human_SNP_ID_670932548 m1A Human chr19 - 58258586 58258586 58258586 CCAGCACTCTCACACGTGGTGCCCTCACACCCAGCACCCTCACACCCAGCACCCTCACACCTGGT CCAGCACTCTCACACGTGGTGCCCTCACACCCGGCACCCTCACACCCAGCACCCTCACACCTGGT T C AC020915.3 Ensembl:ENSG00000268516 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58258336..58258697;chr19:58258325..58258679 26863196 MeRIP-seq:(Medium) rs1216474705 Functional Loss SNV dbSNP153 33..33 33 - - - 70985 RMVar_ID_70985 Human_SNP_ID_670933088 m1A Human chr19 + 58260856 58260856 58260856 AACTTAGGCATTTTGGATTTCTTTCAGACTGGAAAGCTACCCTTGAGGAGAATAGGTTGAATTCT AACTTAGGCATTTTGGATTTCTTTCAGACTGGGAAGCTACCCTTGAGGAGAATAGGTTGAATTCT A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58260851..58260962 26863196 MeRIP-seq:(Medium) rs573833360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55632,Human_RBP_ID_18741164,Human_RBP_ID_22976744 Human_Splice_Rec_2051374,Human_Splice_Rec_2051404,Human_Splice_Rec_2051430,Human_Splice_Rec_2051446,Human_Splice_Rec_2051458,Human_Splice_Rec_2051464,Human_Splice_Rec_2051474,Human_Splice_Rec_2051482,Human_Splice_Rec_2051490,Human_Splice_Rec_2051538 RMVar_hsa_circ_196496,RMVar_hsa_circ_196495,RMVar_hsa_circ_196497,RMVar_hsa_circ_269509 70986 RMVar_ID_70986 Human_SNP_ID_670933405 m1A Human chr19 - 58261626 58261626 58261626 TCTGTAGTCTGAATGATGTTACAGTCAGAAAAAGATGAGGCCATGGGGAAGGCAGCACAGCGTTC TCTGTAGTCTGAATGATGTTACAGTCAGAAAACGATGAGGCCATGGGGAAGGCAGCACAGCGTTC T G AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:58261477..58261650 26863196 MeRIP-seq:(Medium) rs1400887594 Functional Loss SNV dbSNP153 33..33 33 - - - 70987 RMVar_ID_70987 Human_SNP_ID_670938580 m1A Human chr19 - 58278603 58278600 58278603 GACCTGCTCTTCTCGGGAACTTGCGCGGGAGGAGGCCCGGAGCTGCGCCGCTTTACCCTCTGCTC GACCTGCTCTTCTCGGGAACTTGCGCGGGAGG___CCCGGAGCTGCGCCGCTTTACCCTCTGCTC GCCT G AC020915.3 Ensembl:ENSG00000268516 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58278554..58278679 26863196 MeRIP-seq:(Medium) rs1568520784 Functional Loss DEL dbSNP153 33..35 33 - - - Human_Splice_Rec_2051571 70988 RMVar_ID_70988 Human_SNP_ID_670938772 m1A Human chr19 - 58279083 58279083 58279083 TCACTCCCGCTACCCCTTCGTCCTCGGGGTCCATGCTGGATCGCCCAGTGAAGGACAGCGCCTGA TCACTCCCGCTACCCCTTCGTCCTCGGGGTCCCTGCTGGATCGCCCAGTGAAGGACAGCGCCTGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58279032..58279150 26863196 MeRIP-seq:(Medium) rs1038584613 Functional Loss SNV dbSNP153 33..33 33 - - - 70989 RMVar_ID_70989 Human_SNP_ID_670939413 m1A Human chr19 + 58281262 58281262 58281262 GGAGATACTGGCAGCTCAACTAAGGCAGTGGGAAAAAGAGAGGAGTGGTTAGGCCCAGTGACCAG GGAGATACTGGCAGCTCAACTAAGGCAGTGGGGAAAAGAGAGGAGTGGTTAGGCCCAGTGACCAG A G ZNF8,AC020915.5,AC020915.1 Ensembl:ENSG00000278129,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58281260..58281464 26863196 MeRIP-seq:(Medium) rs548274828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13525210 RMVar_hsa_circ_125998,RMVar_hsa_circ_196499 70990 RMVar_ID_70990 Human_SNP_ID_670945764 m1A Human chr19 - 58305427 58305427 58305427 CACACACCACTCACCACTGTGGCAGCCTCCTCAGAGAGCCTAGCCGCCCGATAGTCCGCGCGCCC CACACACCACTCACCACTGTGGCAGCCTCCTCGGAGAGCCTAGCCGCCCGATAGTCCGCGCGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:58305376..58305482;chr19:58305376..58312280;chr19:58305376..58305566;chr19:58305376..58305502 26863196 MeRIP-seq:(Medium) rs746030534 Functional Loss SNV dbSNP153 33..33 33 - - - 70991 RMVar_ID_70991 Human_SNP_ID_670950534 m1A Human chr19 - 58325124 58325124 58325124 ATGGAACACAAATGCCCACGTCAGGAGGAGGCATGGATGAGGAAGACTGGCTGGGGTGGATTAAG ATGGAACACAAATGCCCACGTCAGGAGGAGGCGTGGATGAGGAAGACTGGCTGGGGTGGATTAAG T C AC010642.2 Ensembl:ENSG00000283103 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58325120..58325288 26863196 MeRIP-seq:(Medium) rs1007510348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23809947 70992 RMVar_ID_70992 Human_SNP_ID_670951166 m1A Human chr19 + 58326867 58326867 58326867 CCTTTCGCGCATCGCCTGCTGCTCTCCCACTCAGCGCCACCTCAGTCCCACAAAGGCCGGGCTGG CCTTTCGCGCATCGCCTGCTGCTCTCCCACTCGGCGCCACCTCAGTCCCACAAAGGCCGGGCTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58326547..58326866 26863196 MeRIP-seq:(Medium) rs573581826 Functional Loss SNV dbSNP153 33..33 33 - - - 70993 RMVar_ID_70993 Human_SNP_ID_670951261 m1A Human chr19 + 58327147 58327147 58327147 GTGGGTTTCGGGGGTGTTCTCCGTCCTGATCCAGGCTGGAGAGGGGCACAGCAGGTCCAGAAGCC GTGGGTTTCGGGGGTGTTCTCCGTCCTGATCCGGGCTGGAGAGGGGCACAGCAGGTCCAGAAGCC A G ZSCAN22 Ensembl:ENSG00000182318 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58327050..58327182 26863196 MeRIP-seq:(Medium) rs562957850 Functional Loss SNV dbSNP153 33..33 33 - - - 70994 RMVar_ID_70994 Human_SNP_ID_670962053 m1A Human chr19 - 58361928 58361928 58361928 CGAGGACGGACTCAGGACGGCAGCCCTGATAGATGCGGCTGGGGGCTGGCGGGTCGGGGTCGCAC CGAGGACGGACTCAGGACGGCAGCCCTGATAGTTGCGGCTGGGGGCTGGCGGGTCGGGGTCGCAC T A AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58361844..58362159 26863196 MeRIP-seq:(Medium) rs1337121459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5088949 70995 RMVar_ID_70995 Human_SNP_ID_670962063 m1A Human chr19 - 58361958 58361958 58361958 ACCTTACGGGGCTCACATGCTATCCCACGACGAGGACGGACTCAGGACGGCAGCCCTGATAGATG ACCTTACGGGGCTCACATGCTATCCCACGACGGGGACGGACTCAGGACGGCAGCCCTGATAGATG T C AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58361955..58362147 26863196 MeRIP-seq:(Medium) rs1465205072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587146 70996 RMVar_ID_70996 Human_SNP_ID_670964477 m1A Human chr19 - 58368571 58368571 58368571 AAGAGTCCCCCAGTGTGTCCTGAGTGCGGCCAAACCTCGCGACCTCGCCCTATTGTCCCCGACCC AAGAGTCCCCCAGTGTGTCCTGAGTGCGGCCACACCTCGCGACCTCGCCCTATTGTCCCCGACCC T G ZNF837 Ensembl:ENSG00000152475 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58368564..58368662 26863196 MeRIP-seq:(Medium) rs1380207372 Functional Loss SNV dbSNP153 33..33 33 - - - 70997 RMVar_ID_70997 Human_SNP_ID_670968510 m1A Human chr19 - 58381410 58381410 58381410 TCTGACTCGCAACGCGCTCACCAAGACACTTCAGAGCTCCCCAGGTGCTTCCCAGCCCAACTCTC TCTGACTCGCAACGCGCTCACCAAGACACTTCGGAGCTCCCCAGGTGCTTCCCAGCCCAACTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58381401..58381492 26863196 MeRIP-seq:(Medium) rs1568570436 Functional Loss SNV dbSNP153 33..33 33 - - - 70998 RMVar_ID_70998 Human_SNP_ID_670970208 m1A Human chr19 + 58387319 58387319 58387319 GGGCGGCGCGTGGTCTACGCCGAGTGACAGAGACGCTCAGGCTGTGTTCTCAGGTGAGACCGCCG GGGCGGCGCGTGGTCTACGCCGAGTGACAGAGGCGCTCAGGCTGTGTTCTCAGGTGAGACCGCCG A G RPS5 Ensembl:ENSG00000083845 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:58387301..58387350 26863196 MeRIP-seq:(Medium) rs1230670071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239278,Human_RBP_ID_528372,Human_RBP_ID_770206,Human_RBP_ID_1573686,Human_RBP_ID_1893286,Human_RBP_ID_3578415,Human_RBP_ID_4557741,Human_RBP_ID_8495791,Human_RBP_ID_9329243,Human_RBP_ID_13526209,Human_RBP_ID_17655392,Human_RBP_ID_17696557,Human_RBP_ID_18192525,Human_RBP_ID_18741331,Human_RBP_ID_19094398,Human_RBP_ID_22449669,Human_RBP_ID_22533217,Human_RBP_ID_23810048,Human_RBP_ID_26769885,Human_RBP_ID_27157954 Human_Splice_Rec_2051829,Human_Splice_Rec_2051849,Human_Splice_Rec_2051857,Human_Splice_Rec_2051869,Human_Splice_Rec_2051879,Human_Splice_Rec_2051881 RMVar_hsa_circ_76022,RMVar_hsa_circ_119921,RMVar_hsa_circ_109868,RMVar_hsa_circ_112811,RMVar_hsa_circ_92126,RMVar_hsa_circ_196509,RMVar_hsa_circ_196511,RMVar_hsa_circ_196512,RMVar_hsa_circ_196510,RMVar_hsa_circ_196508 70999 RMVar_ID_70999 Human_SNP_ID_670970213 m1A Human chr19 + 58387338 58387338 58387338 CCGAGTGACAGAGACGCTCAGGCTGTGTTCTCAGGTGAGACCGCCGCGGGGCCGGGGATCCTAGG CCGAGTGACAGAGACGCTCAGGCTGTGTTCTCGGGTGAGACCGCCGCGGGGCCGGGGATCCTAGG A G RPS5 Ensembl:ENSG00000083845 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:58387251..58387375;chr19:58387276..58387403;chr19:58387276..58387350 26863410,32194978,32194978 MeRIP-seq:(Medium) rs1489370744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239278,Human_RBP_ID_528373,Human_RBP_ID_770206,Human_RBP_ID_912659,Human_RBP_ID_1573689,Human_RBP_ID_1893286,Human_RBP_ID_3578415,Human_RBP_ID_4558827,Human_RBP_ID_9329243,Human_RBP_ID_17655392,Human_RBP_ID_18192526,Human_RBP_ID_19091023,Human_RBP_ID_22449670,Human_RBP_ID_22533217,Human_RBP_ID_23810048,Human_RBP_ID_26470661,Human_RBP_ID_26769885,Human_RBP_ID_26996523 Human_Splice_Rec_2051829,Human_Splice_Rec_2051849,Human_Splice_Rec_2051857,Human_Splice_Rec_2051869,Human_Splice_Rec_2051879,Human_Splice_Rec_2051881 RMVar_hsa_circ_76022,RMVar_hsa_circ_119921,RMVar_hsa_circ_109868,RMVar_hsa_circ_112811,RMVar_hsa_circ_92126,RMVar_hsa_circ_196509,RMVar_hsa_circ_196511,RMVar_hsa_circ_196512,RMVar_hsa_circ_196510,RMVar_hsa_circ_196508 71000 RMVar_ID_71000 Human_SNP_ID_670970469 m1A Human chr19 - 58388086 58388086 58388086 AGGAAAAAAACGTCAGAGCTCAGCTAGCATGGAGCAAAGGCGCACTCATTCCCAACTCTGAGGCT AGGAAAAAAACGTCAGAGCTCAGCTAGCATGGTGCAAAGGCGCACTCATTCCCAACTCTGAGGCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58388081..58388304 26863196 MeRIP-seq:(Medium) rs1433831579 Functional Loss SNV dbSNP153 33..33 33 - - - 71001 RMVar_ID_71001 Human_SNP_ID_670970473 m1A Human chr19 - 58388097 58388097 58388097 AGGGTGATGACAGGAAAAAAACGTCAGAGCTCAGCTAGCATGGAGCAAAGGCGCACTCATTCCCA AGGGTGATGACAGGAAAAAAACGTCAGAGCTCCGCTAGCATGGAGCAAAGGCGCACTCATTCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58388093..58388286 26863196 MeRIP-seq:(Medium) rs1381606604 Functional Loss SNV dbSNP153 33..33 33 - - - 71002 RMVar_ID_71002 Human_SNP_ID_670970521 m1A Human chr19 - 58388230 58388230 58388230 CACCAAGTTCCCCTCACCTGCAGGGAAATGTCATTGATCTGCACATCATCGGTGCTCCACTTCCC CACCAAGTTCCCCTCACCTGCAGGGAAATGTCGTTGATCTGCACATCATCGGTGCTCCACTTCCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58388126..58388295 32194978 MeRIP-seq:(Medium) rs1296966117 Functional Loss SNV dbSNP153 33..33 33 - - - 71003 RMVar_ID_71003 Human_SNP_ID_670970522 m1A Human chr19 - 58388236 58388236 58388236 GCCAATCACCAAGTTCCCCTCACCTGCAGGGAAATGTCATTGATCTGCACATCATCGGTGCTCCA GCCAATCACCAAGTTCCCCTCACCTGCAGGGATATGTCATTGATCTGCACATCATCGGTGCTCCA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58388097..58388296 26863410 MeRIP-seq:(Medium) rs757135639 Functional Loss SNV dbSNP153 33..33 33 - - - 71004 RMVar_ID_71004 Human_SNP_ID_670972070 m1A Human chr19 + 58393034 58393034 58393034 TGCCAAGTACCTGCCTCACAGTGCAGGGCGGTATGCCGCCAAACGCTTCCGCAAAGCTCAGTGTC TGCCAAGTACCTGCCTCACAGTGCAGGGCGGTGTGCCGCCAAACGCTTCCGCAAAGCTCAGTGTC A G RPS5 Ensembl:ENSG00000083845 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:58392941..58393169;chr19:58392930..58393208 26863196 MeRIP-seq:(Medium) rs759592801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528382,Human_RBP_ID_823843,Human_RBP_ID_1573697,Human_RBP_ID_4551785,Human_RBP_ID_8495807,Human_RBP_ID_9090339,Human_RBP_ID_17933140,Human_RBP_ID_18192528,Human_RBP_ID_22448039,Human_RBP_ID_22812677,Human_RBP_ID_23211049,Human_RBP_ID_23810058,Human_RBP_ID_26818029,Human_RBP_ID_27279374 Human_Splice_Rec_2051832,Human_Splice_Rec_2051842,Human_Splice_Rec_2051862,Human_Splice_Rec_2051872,Human_Splice_Rec_2051884,Human_Splice_Rec_2051888 RMVar_hsa_circ_119921,RMVar_hsa_circ_109868,RMVar_hsa_circ_92126,RMVar_hsa_circ_196514,RMVar_hsa_circ_105536,RMVar_hsa_circ_196511,RMVar_hsa_circ_196512,RMVar_hsa_circ_196510,RMVar_hsa_circ_88518,RMVar_hsa_circ_89509,RMVar_hsa_circ_196516,RMVar_hsa_circ_41293,RMVar_hsa_circ_196515,RMVar_hsa_circ_122772,RMVar_hsa_circ_274880,RMVar_hsa_circ_196518,RMVar_hsa_circ_99562,RMVar_hsa_circ_196519,RMVar_hsa_circ_196517 71005 RMVar_ID_71005 Human_SNP_ID_670972542 m1A Human chr19 - 58394559 58394559 58394559 GCAGCATTGATGAGCTCATCTGCCAGGCACTCAGCAATGGTCTTAATGTTCCGGAAGGCAGCCTC GCAGCATTGATGAGCTCATCTGCCAGGCACTCGGCAATGGTCTTAATGTTCCGGAAGGCAGCCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58394476..58394806 32194978 MeRIP-seq:(Medium) rs905465944 Functional Loss SNV dbSNP153 33..33 33 - - - 71006 RMVar_ID_71006 Human_SNP_ID_670974655 m1A Human chr19 + 58401140 58401140 58401140 GCATACGAATCTGGGTCCTGGAAGCGTTCTGCAAGATCCCTTCTCACCTCAACCGCACGTGCTGG GCATACGAATCTGGGTCCTGGAAGCGTTCTGCGAGATCCCTTCTCACCTCAACCGCACGTGCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58401132..58401219 26863196 MeRIP-seq:(Medium) rs373159138 Functional Loss SNV dbSNP153 33..33 33 - - - 71007 RMVar_ID_71007 Human_SNP_ID_670974833 m1A Human chr19 - 58401573 58401573 58401573 GCCGCAGCCTTTCCTCTCGCCAGCGCCATCGGAGTGCTGGTGCTCACTGTTCTCACCACTCGCTC GCCGCAGCCTTTCCTCTCGCCAGCGCCATCGGGGTGCTGGTGCTCACTGTTCTCACCACTCGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58401536..58401686 26863196 MeRIP-seq:(Medium) rs1358948663 Functional Loss SNV dbSNP153 33..33 33 - - - 71008 RMVar_ID_71008 Human_SNP_ID_670975925 m1A Human chr19 + 58404906 58404865 58404906 CCCCACCTCCCTCCTGGACGGGGCGGCTGGCCAGGCAGAGGGGCTCCTCACTTCCCAGTAGGGGC _________________________________GGCAGAGGGGCTCCTCACTTCCCAGTAGGGGC GACCCCCCCCCCCACCTCCCTCCTGGACGGGGCGGCTGGCCA G ZNF584 Ensembl:ENSG00000171574 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58404811..58405178 26863410 MeRIP-seq:(Medium) rs1287797088 Functional Loss DEL dbSNP153 1..33 33 - - - 71009 RMVar_ID_71009 Human_SNP_ID_670975971 m1A Human chr19 + 58404906 58404906 58404906 CCCCACCTCCCTCCTGGACGGGGCGGCTGGCCAGGCAGAGGGGCTCCTCACTTCCCAGTAGGGGC CCCCACCTCCCTCCTGGACGGGGCGGCTGGCCGGGCAGAGGGGCTCCTCACTTCCCAGTAGGGGC A G ZNF584 Ensembl:ENSG00000171574 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58404811..58405178 26863410 MeRIP-seq:(Medium) rs1479515093 Functional Loss SNV dbSNP153 33..33 33 - - - 71010 RMVar_ID_71010 Human_SNP_ID_670977260 m1A Human chr19 - 58407870 58407870 58407870 GGTATGGGGGCCTGGGAGAGGAGAGTGAGTACATGGCTGAGTACGTCAGAGCACGGGGTCAGGGA GGTATGGGGGCCTGGGAGAGGAGAGTGAGTACGTGGCTGAGTACGTCAGAGCACGGGGTCAGGGA T C AC012313.1 Ensembl:ENSG00000232098 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58407827..58407934 26863196 MeRIP-seq:(Medium) rs1159210924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824313,Human_RBP_ID_4560376,Human_RBP_ID_5586415,Human_RBP_ID_13526604,Human_RBP_ID_23810089 71011 RMVar_ID_71011 Human_SNP_ID_670977444 m1A Human chr19 - 58408401 58408401 58408401 AGGAGTCTCCGCTGGTCCGCAGAAACGAACGAAGGCGCGAGAATCGGGAAGTTCTGCCTCAGTGA AGGAGTCTCCGCTGGTCCGCAGAAACGAACGAGGGCGCGAGAATCGGGAAGTTCTGCCTCAGTGA T C AC012313.1 Ensembl:ENSG00000232098 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:58408352..58408450;chr19:58408350..58408435 26863196 MeRIP-seq:(Medium) rs890194291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575279,Human_RBP_ID_5586869,Human_RBP_ID_5651233,Human_RBP_ID_9425491,Human_RBP_ID_18421004,Human_RBP_ID_22071745,Human_RBP_ID_22719326 71012 RMVar_ID_71012 Human_SNP_ID_670977447 m1A Human chr19 - 58408411 58408411 58408411 GGCGGTGTGGAGGAGTCTCCGCTGGTCCGCAGAAACGAACGAAGGCGCGAGAATCGGGAAGTTCT GGCGGTGTGGAGGAGTCTCCGCTGGTCCGCAGTAACGAACGAAGGCGCGAGAATCGGGAAGTTCT T A AC012313.1 Ensembl:ENSG00000232098 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58408221..58408459 26863196 MeRIP-seq:(Medium) rs1287429834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575279,Human_RBP_ID_4558830,Human_RBP_ID_5586869,Human_RBP_ID_5651233,Human_RBP_ID_8200035,Human_RBP_ID_9425491,Human_RBP_ID_18421004,Human_RBP_ID_22071745,Human_RBP_ID_22719326 71013 RMVar_ID_71013 Human_SNP_ID_670977593 m1A Human chr19 - 58408745 58408737 58408746 TGCGGACTGCCGGGCAACGCCGGAACTCCCGGAACTCCCGTGGCCCGCGCCTCCCCTCGCTCGGC TGCGGACTGCCGGGCAACGCCGGAACTCCCG_________TGGCCCGCGCCTCCCCTCGCTCGGC ACGGGAGTTC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:58408698..58408965;chr19:58408699..58408825 26863196 MeRIP-seq:(Medium) rs145105239 Functional Loss DEL dbSNP153 32..40 33 - - - 71014 RMVar_ID_71014 Human_SNP_ID_670977597 m1A Human chr19 - 58408745 58408745 58408745 TGCGGACTGCCGGGCAACGCCGGAACTCCCGGAACTCCCGTGGCCCGCGCCTCCCCTCGCTCGGC TGCGGACTGCCGGGCAACGCCGGAACTCCCGGCACTCCCGTGGCCCGCGCCTCCCCTCGCTCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:58408698..58408965;chr19:58408699..58408825 26863196 MeRIP-seq:(Medium) rs1340458767 Functional Loss SNV dbSNP153 33..33 33 - - - 71015 RMVar_ID_71015 Human_SNP_ID_670977991 m1A Human chr19 + 58409951 58409951 58409951 TCTGCCCATCATTGACCCCAAGGCTCAGTTGGACCCATCATTGCAGGGCTTGGTGATGTTTGAGG TCTGCCCATCATTGACCCCAAGGCTCAGTTGGGCCCATCATTGCAGGGCTTGGTGATGTTTGAGG A G ZNF584 Ensembl:ENSG00000171574 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58409948..58410049 26863196 MeRIP-seq:(Medium) rs936255467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13554337 Human_Splice_Rec_2051906 71016 RMVar_ID_71016 Human_SNP_ID_670981066 m1A Human chr19 + 58418276 58418276 58418276 TATTTGTCATGCCCTAGCATGGACTGTCTCATACTGCTCTGGACTATGTGGTAATAAAGGCTTTA TATTTGTCATGCCCTAGCATGGACTGTCTCATGCTGCTCTGGACTATGTGGTAATAAAGGCTTTA A G ZNF584 Ensembl:ENSG00000171574 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58418226..58418327 32194978 MeRIP-seq:(Medium) rs762067240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528446,Human_RBP_ID_1573754,Human_RBP_ID_1893312,Human_RBP_ID_3578445,Human_RBP_ID_4558835,Human_RBP_ID_13526665,Human_RBP_ID_27472163 Human_miRNA_ID_2253474,Human_miRNA_ID_2826157,Human_miRNA_ID_2860130 RMVar_hsa_circ_94643,RMVar_hsa_circ_93416,RMVar_hsa_circ_196525,RMVar_hsa_circ_97541,RMVar_hsa_circ_196526,RMVar_hsa_circ_196527 71017 RMVar_ID_71017 Human_SNP_ID_670991414 m1A Human chr19 - 58453622 58453608 58453622 TGGCTGTGAGCCAGGACCAAGCTCCCCATCCCAACAGTCACCTCCCCCAGTGTCCCTCCTTCCTT TGGCTGTGAGCCAGGACCAAGCTCCCCATCCC______________CCAGTGTCCCTCCTTCCTT GGGGAGGTGACTGTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58453615..58453698 26863196 MeRIP-seq:(Medium) rs201227400 Functional Loss DEL dbSNP153 33..46 33 - - - 71018 RMVar_ID_71018 Human_SNP_ID_670996145 m1A Human chr19 + 58469145 58469145 58469145 AGGGAAGCCAAAAGATTGGATAACCCAGCCTTAGACCATGGCTGTCTCTTCCTCCCTGCTCTTTT AGGGAAGCCAAAAGATTGGATAACCCAGCCTTGGACCATGGCTGTCTCTTCCTCCCTGCTCTTTT A G ZNF324 Ensembl:ENSG00000083812 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58469134..58469207 26863196 MeRIP-seq:(Medium) rs1398384342 Functional Loss SNV dbSNP153 33..33 33 - - - 71019 RMVar_ID_71019 Human_SNP_ID_670999324 m1A Human chr19 + 58476697 58476697 58476697 GCGAGCACGATGTCCACGTGCCCCCTCCCCAGAGCCATTCCTAAAGGAGGTCCCACCCAGTCAAC GCGAGCACGATGTCCACGTGCCCCCTCCCCAGGGCCATTCCTAAAGGAGGTCCCACCCAGTCAAC A G ZNF446 Ensembl:ENSG00000083838 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58476694..58476892 26863196 MeRIP-seq:(Medium) rs1216166505 Functional Loss SNV dbSNP153 33..33 33 - - - 71020 RMVar_ID_71020 Human_SNP_ID_670999333 m1A Human chr19 - 58476725 58476725 58476725 ACGAGTCGCCCTCCACAATCTCGGGGAGGTTGACTGGGTGGGACCTCCTTTAGGAATGGCTCTGG ACGAGTCGCCCTCCACAATCTCGGGGAGGTTGGCTGGGTGGGACCTCCTTTAGGAATGGCTCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58476715..58476900 26863196 MeRIP-seq:(Medium) rs775112755 Functional Loss SNV dbSNP153 33..33 33 - - - 71021 RMVar_ID_71021 Human_SNP_ID_670999595 m1A Human chr19 + 58477325 58477325 58477325 CCGCCTCCGCTTCCGAGGGTTCTGCTACCAGGAGGTGGCAGGTCCCCGAGAAGCCCTGGCCCGGC CCGCCTCCGCTTCCGAGGGTTCTGCTACCAGGTGGTGGCAGGTCCCCGAGAAGCCCTGGCCCGGC A T ZNF446 Ensembl:ENSG00000083838 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58477275..58477425 32194978 MeRIP-seq:(Medium) rs200797935 Functional Loss SNV dbSNP153 33..33 33 - - - 71022 RMVar_ID_71022 Human_SNP_ID_670999854 m1A Human chr19 - 58477773 58477773 58477773 TGGGCTCCTCCTTCACACTGCAGCTGAGCTGGACAGACCCCTCTATTCTGGTGTCCTGGGGACCT TGGGCTCCTCCTTCACACTGCAGCTGAGCTGGGCAGACCCCTCTATTCTGGTGTCCTGGGGACCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58477723..58477823 32194978 MeRIP-seq:(Medium) rs1323106913 Functional Loss SNV dbSNP153 33..33 33 - - - 71023 RMVar_ID_71023 Human_SNP_ID_671003803 m1A Human chr19 - 58489366 58489366 58489366 ACAGAGTCGAAGCTGTCGTCTTGCGCGGAGTCAGTTCCTGGGGGCCACAAGATCAGATGAGCCAT ACAGAGTCGAAGCTGTCGTCTTGCGCGGAGTCGGTTCCTGGGGGCCACAAGATCAGATGAGCCAT T C SLC27A5 Ensembl:ENSG00000083807 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58489359..58489432 26863196 MeRIP-seq:(Medium) rs547386852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13527080 Human_miRNA_ID_2454629,Human_miRNA_ID_2470088,Human_miRNA_ID_3089257 RMVar_hsa_circ_122226,RMVar_hsa_circ_196534 71024 RMVar_ID_71024 Human_SNP_ID_671006703 m1A Human chr19 + 58498638 58498638 58498638 GGGTCAACCACGATCCCCACATTGAAGCCCTCACGCACCAACCGGGTCTTCATCAGTTTGAACGT GGGTCAACCACGATCCCCACATTGAAGCCCTCGCGCACCAACCGGGTCTTCATCAGTTTGAACGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58498589..58498680 26863196 MeRIP-seq:(Medium) rs758978250 Functional Loss SNV dbSNP153 33..33 33 - - - 71025 RMVar_ID_71025 Human_SNP_ID_671006818 m1A Human chr19 + 58498890 58498890 58498890 TCGAAAGTCTGGCCGGGGGCTAGCTGCACAGCAGCCATGCCCACCTTACCCTCACAACCTAGAGA TCGAAAGTCTGGCCGGGGGCTAGCTGCACAGCCGCCATGCCCACCTTACCCTCACAACCTAGAGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58498841..58498969 26863196 MeRIP-seq:(Medium) rs775274046 Functional Loss SNV dbSNP153 33..33 33 - - - 71026 RMVar_ID_71026 Human_SNP_ID_671006819 m1A Human chr19 - 58498895 58498895 58498895 ACTGCTCTCTAGGTTGTGAGGGTAAGGTGGGCATGGCTGCTGTGCAGCTAGCCCCCGGCCAGACT ACTGCTCTCTAGGTTGTGAGGGTAAGGTGGGCTTGGCTGCTGTGCAGCTAGCCCCCGGCCAGACT T A SLC27A5 Ensembl:ENSG00000083807 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58498844..58498946 26863196 MeRIP-seq:(Medium) rs987994295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528514,Human_RBP_ID_915196,Human_RBP_ID_4552226,Human_RBP_ID_5321956,Human_RBP_ID_17657410 Human_Splice_Rec_2052080,Human_Splice_Rec_2052088,Human_Splice_Rec_2052106,Human_Splice_Rec_2052126 RMVar_hsa_circ_117835,RMVar_hsa_circ_122226,RMVar_hsa_circ_196534,RMVar_hsa_circ_75916,RMVar_hsa_circ_112406,RMVar_hsa_circ_196535,RMVar_hsa_circ_196536,RMVar_hsa_circ_196537,RMVar_hsa_circ_96401,RMVar_hsa_circ_196538 71027 RMVar_ID_71027 Human_SNP_ID_671007228 m1A Human chr19 + 58499837 58499837 58499837 AAGACACAGACAGGGAGATCCAGAGATGAGAGAGACATTCAGAGACCTTGAGAGACTGCGACAAG AAGACACAGACAGGGAGATCCAGAGATGAGAGGGACATTCAGAGACCTTGAGAGACTGCGACAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58499830..58499967 26863196 MeRIP-seq:(Medium) rs76693695 Functional Loss SNV dbSNP153 33..33 33 - - - 71028 RMVar_ID_71028 Human_SNP_ID_671008016 m1A Human chr19 + 58502435 58502431 58502436 GTGAGTGAGAAGATGGATGTGTGGACAGTTAGAGTAGTGAGTGAGAAGATGGATGGGTGAACAGA GTGAGTGAGAAGATGGATGTGTGGACAGT_____TAGTGAGTGAGAAGATGGATGGGTGAACAGA TTAGAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58502384..58502491 26863196 MeRIP-seq:(Medium) rs1163836194 Functional Loss DEL dbSNP153 30..34 33 - - - 71029 RMVar_ID_71029 Human_SNP_ID_671008024 m1A Human chr19 + 58502449 58502447 58502449 GGATGTGTGGACAGTTAGAGTAGTGAGTGAGAAGATGGATGGGTGAACAGAGTAGTGAGTGAGTA GGATGTGTGGACAGTTAGAGTAGTGAGTGAGA_GATGGATGGGTGAACAGAGTAGTGAGTGAGTA GAA GA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58502402..58502485 26863196 MeRIP-seq:(Medium) rs879233678 Functional Loss DEL dbSNP153 33..33 33 - - - 71030 RMVar_ID_71030 Human_SNP_ID_671008027 m1A Human chr19 + 58502449 58502449 58502449 GGATGTGTGGACAGTTAGAGTAGTGAGTGAGAAGATGGATGGGTGAACAGAGTAGTGAGTGAGTA GGATGTGTGGACAGTTAGAGTAGTGAGTGAGAGGATGGATGGGTGAACAGAGTAGTGAGTGAGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58502402..58502485 26863196 MeRIP-seq:(Medium) rs1490779591 Functional Loss SNV dbSNP153 33..33 33 - - - 71031 RMVar_ID_71031 Human_SNP_ID_671008114 m1A Human chr19 + 58502646 58502646 58502646 AGTGAGAAGATGGATGTGTGGACAGAGTAGTGAGTGAGAAGATGGATGGGTGAACAGTTAGAGTA AGTGAGAAGATGGATGTGTGGACAGAGTAGTGGGTGAGAAGATGGATGGGTGAACAGTTAGAGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:58502597..58502697;chr19:58502590..58502703 26863196 MeRIP-seq:(Medium) rs1251828351 Functional Loss SNV dbSNP153 33..33 33 - - - 71032 RMVar_ID_71032 Human_SNP_ID_671008179 m1A Human chr19 + 58502783 58502779 58502784 GTGAGTGAGTAGATGGATGGGTGGACAGTTAGAGTAGTGAGTGAGTAGATGGATGGCTGGACAGT GTGAGTGAGTAGATGGATGGGTGGACAGT_____TAGTGAGTGAGTAGATGGATGGCTGGACAGT TTAGAG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58502771..58502856 26863196 MeRIP-seq:(Medium) rs1345912475 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_23810192 71033 RMVar_ID_71033 Human_SNP_ID_671008197 m1A Human chr19 - 58502821 58502821 58502821 TAACTGTCCACCCATCCATCTACTCACTCACTACTCTAACTGTCCAGCCATCCATCTACTCACTC TAACTGTCCACCCATCCATCTACTCACTCACTCCTCTAACTGTCCAGCCATCCATCTACTCACTC T G SLC27A5 Ensembl:ENSG00000083807 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr19:58502772..58502885;chr19:58502758..58502921 26863196 MeRIP-seq:(Medium) rs1264936132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112406,RMVar_hsa_circ_196537 71034 RMVar_ID_71034 Human_SNP_ID_671013103 m1A Human chr19 + 58517887 58517887 58517887 CACTCCCTCCTCCCCCTACCTCAGACCTGGCCAGGCCGTCTACAGCCCCCCATTAACGCTGCAAA CACTCCCTCCTCCCCCTACCTCAGACCTGGCCCGGCCGTCTACAGCCCCCCATTAACGCTGCAAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58517632..58517965 26863196 MeRIP-seq:(Medium) rs575165520 Functional Loss SNV dbSNP153 33..33 33 - - - 71035 RMVar_ID_71035 Human_SNP_ID_671021331 m1A Human chr19 - 58544172 58544172 58544172 GAGTGTGATTCCCCTCTCAGCTCCACCTCCAGACCACACAGAAGCGGGCCGCTGTGCGCCCAAGC GAGTGTGATTCCCCTCTCAGCTCCACCTCCAGGCCACACAGAAGCGGGCCGCTGTGCGCCCAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58544122..58544193 26863196 MeRIP-seq:(Medium) rs73580853 Functional Loss SNV dbSNP153 33..33 33 - - - 71036 RMVar_ID_71036 Human_SNP_ID_671021551 m1A Human chr19 - 58544517 58544517 58544517 CCGCCCGCGCTTCTTCCTCAGCCGCCGCCGAAACCCGCACCACGCGCCACAAGCACAAGCACAAC CCGCCCGCGCTTCTTCCTCAGCCGCCGCCGAATCCCGCACCACGCGCCACAAGCACAAGCACAAC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58544451..58544775 26863196 MeRIP-seq:(Medium) rs1195971956 Functional Loss SNV dbSNP153 33..33 33 - - - 71037 RMVar_ID_71037 Human_SNP_ID_671021612 m1A Human chr19 + 58544666 58544657 58544666 GCGGCGCTCGGCCTCGCGGCGGCGGCGGCGGCAGCGGCCCAGCAGTTGGCGGCGAGCGCGTCTGC GCGGCGCTCGGCCTCGCGGCGGCG_________GCGGCCCAGCAGTTGGCGGCGAGCGCGTCTGC GGCGGCGGCA G TRIM28 Ensembl:ENSG00000130726 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:58544480..58544810 26863410 MeRIP-seq:(Medium) rs1043564348 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4557745,Human_RBP_ID_5320612,Human_RBP_ID_5527188,Human_RBP_ID_9293965,Human_RBP_ID_9329247 RMVar_hsa_circ_80256,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90674,RMVar_hsa_circ_196540,RMVar_hsa_circ_196542,RMVar_hsa_circ_196543,RMVar_hsa_circ_196541 71038 RMVar_ID_71038 Human_SNP_ID_671021619 m1A Human chr19 + 58544666 58544666 58544666 GCGGCGCTCGGCCTCGCGGCGGCGGCGGCGGCAGCGGCCCAGCAGTTGGCGGCGAGCGCGTCTGC GCGGCGCTCGGCCTCGCGGCGGCGGCGGCGGCGGCGGCCCAGCAGTTGGCGGCGAGCGCGTCTGC A G TRIM28 Ensembl:ENSG00000130726 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:58544480..58544810 26863410 MeRIP-seq:(Medium) rs1007878177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557745,Human_RBP_ID_5320612,Human_RBP_ID_5527188,Human_RBP_ID_9293965,Human_RBP_ID_9329247 RMVar_hsa_circ_80256,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90674,RMVar_hsa_circ_196540,RMVar_hsa_circ_196542,RMVar_hsa_circ_196543,RMVar_hsa_circ_196541 71039 RMVar_ID_71039 Human_SNP_ID_671021971 m1A Human chr19 + 58545374 58545374 58545374 GGGGCCCACCCAGCAGGGGAATGGTGGGGGCCATAACCTGGGTGGGAACTTGTAACAGTCTCCCA GGGGCCCACCCAGCAGGGGAATGGTGGGGGCCGTAACCTGGGTGGGAACTTGTAACAGTCTCCCA A G TRIM28 Ensembl:ENSG00000130726 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58545368..58545455 26863196 MeRIP-seq:(Medium) rs537221411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581713,Human_RBP_ID_5374497,Human_RBP_ID_17655698,Human_RBP_ID_22068899,Human_RBP_ID_22666930 RMVar_hsa_circ_80256,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90674,RMVar_hsa_circ_196540,RMVar_hsa_circ_196542,RMVar_hsa_circ_196543,RMVar_hsa_circ_196541 71040 RMVar_ID_71040 Human_SNP_ID_671022027 m1A Human chr19 + 58545487 58545487 58545487 GCTTCTCCAAAGACATCGTGGAGAATTATTTCATGCGTGATAGTGGCAGCAAGGCTGCCACCGAC GCTTCTCCAAAGACATCGTGGAGAATTATTTCGTGCGTGATAGTGGCAGCAAGGCTGCCACCGAC A G TRIM28 Ensembl:ENSG00000130726 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58545426..58545575 32194978 MeRIP-seq:(Medium) rs1568659200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528537,Human_RBP_ID_1018975,Human_RBP_ID_4574143,Human_RBP_ID_8495963,Human_RBP_ID_8838201,Human_RBP_ID_9292915,Human_RBP_ID_17936674,Human_RBP_ID_18192544,Human_RBP_ID_22240423,Human_RBP_ID_22812699,Human_RBP_ID_23810219,Human_RBP_ID_26816406,Human_RBP_ID_26996783,Human_RBP_ID_27279607,Human_RBP_ID_27684351 Human_Splice_Rec_2052152,Human_Splice_Rec_2052153,Human_Splice_Rec_2052184,Human_Splice_Rec_2052185,Human_Splice_Rec_2052192,Human_Splice_Rec_2052193,Human_Splice_Rec_2052229 RMVar_hsa_circ_80256,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90674,RMVar_hsa_circ_90471,RMVar_hsa_circ_196540,RMVar_hsa_circ_196542,RMVar_hsa_circ_196543,RMVar_hsa_circ_196541,RMVar_hsa_circ_95348,RMVar_hsa_circ_196544,RMVar_hsa_circ_196545 71041 RMVar_ID_71041 Human_SNP_ID_671023474 m1A Human chr19 - 58548912 58548912 58548912 TCCACCTCACCCCCAGGGGAGGTGCCATACTTACCGTTTCACACCTGACACATGGGGCTCTGCAC TCCACCTCACCCCCAGGGGAGGTGCCATACTTGCCGTTTCACACCTGACACATGGGGCTCTGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58548799..58549167;chr19:58548797..58549161 26863196 MeRIP-seq:(Medium) rs111630223 Functional Loss SNV dbSNP153 33..33 33 - - - 71042 RMVar_ID_71042 Human_SNP_ID_671023832 m1A Human chr19 + 58549648 58549648 58549648 GACTGTCACCTGCCGGCCCTGCAGGATGTACCAGGGTGAGTGTGAGGCTGGTGGGGGTCAAGTCT GACTGTCACCTGCCGGCCCTGCAGGATGTACCGGGGTGAGTGTGAGGCTGGTGGGGGTCAAGTCT A G TRIM28 Ensembl:ENSG00000130726 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58549320..58549659 26863196 MeRIP-seq:(Medium) rs1461592105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5372240,Human_RBP_ID_8839571,Human_RBP_ID_9259056,Human_RBP_ID_9294000,Human_RBP_ID_17935112,Human_RBP_ID_18192555,Human_RBP_ID_22447048,Human_RBP_ID_22533515,Human_RBP_ID_23211058 Human_Splice_Rec_2052175,Human_Splice_Rec_2052221,Human_Splice_Rec_2052283,Human_Splice_Rec_2052293,Human_Splice_Rec_2052299 RMVar_hsa_circ_23750,RMVar_hsa_circ_54268,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90471,RMVar_hsa_circ_196540,RMVar_hsa_circ_196541,RMVar_hsa_circ_196545,RMVar_hsa_circ_86731,RMVar_hsa_circ_124378,RMVar_hsa_circ_196546,RMVar_hsa_circ_50866,RMVar_hsa_circ_319482,RMVar_hsa_circ_78255,RMVar_hsa_circ_196550,RMVar_hsa_circ_196551,RMVar_hsa_circ_196549,RMVar_hsa_circ_95363,RMVar_hsa_circ_79670,RMVar_hsa_circ_102080,RMVar_hsa_circ_115157,RMVar_hsa_circ_196552,RMVar_hsa_circ_196553,RMVar_hsa_circ_125255,RMVar_hsa_circ_196555,RMVar_hsa_circ_196556,RMVar_hsa_circ_371509,RMVar_hsa_circ_196558,RMVar_hsa_circ_196562,RMVar_hsa_circ_97376,RMVar_hsa_circ_106461,RMVar_hsa_circ_78437,RMVar_hsa_circ_196563,RMVar_hsa_circ_122992,RMVar_hsa_circ_196564,RMVar_hsa_circ_196565,RMVar_hsa_circ_196567,RMVar_hsa_circ_86699,RMVar_hsa_circ_115929,RMVar_hsa_circ_196566,RMVar_hsa_circ_196568 71043 RMVar_ID_71043 Human_SNP_ID_671023999 m1A Human chr19 + 58550004 58550004 58550004 CCTATTCTGTCACGAACCCTGCCGCCCCCTGCATCAGCTGGCTACCGACTCCACCTTCTCCCTGG CCTATTCTGTCACGAACCCTGCCGCCCCCTGCGTCAGCTGGCTACCGACTCCACCTTCTCCCTGG A G TRIM28 Ensembl:ENSG00000130726 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58549940..58550062 26863196 MeRIP-seq:(Medium) rs1568663130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240272,Human_RBP_ID_528563,Human_RBP_ID_771682,Human_RBP_ID_4552496,Human_RBP_ID_6792200,Human_RBP_ID_8838267,Human_RBP_ID_9292954,Human_RBP_ID_13527458,Human_RBP_ID_17271240,Human_RBP_ID_17502038,Human_RBP_ID_22503970,Human_RBP_ID_22812740 Human_Splice_Rec_2052178,Human_Splice_Rec_2052179,Human_Splice_Rec_2052224,Human_Splice_Rec_2052225,Human_Splice_Rec_2052286,Human_Splice_Rec_2052287,Human_Splice_Rec_2052295,Human_Splice_Rec_2052302,Human_Splice_Rec_2052304,Human_Splice_Rec_2052305 RMVar_hsa_circ_23750,RMVar_hsa_circ_111493,RMVar_hsa_circ_126726,RMVar_hsa_circ_90471,RMVar_hsa_circ_196540,RMVar_hsa_circ_196541,RMVar_hsa_circ_196545,RMVar_hsa_circ_86731,RMVar_hsa_circ_124378,RMVar_hsa_circ_196546,RMVar_hsa_circ_50866,RMVar_hsa_circ_319482,RMVar_hsa_circ_196550,RMVar_hsa_circ_196551,RMVar_hsa_circ_95363,RMVar_hsa_circ_79670,RMVar_hsa_circ_115157,RMVar_hsa_circ_196552,RMVar_hsa_circ_196553,RMVar_hsa_circ_125255,RMVar_hsa_circ_196556,RMVar_hsa_circ_371509,RMVar_hsa_circ_196558,RMVar_hsa_circ_196562,RMVar_hsa_circ_97376,RMVar_hsa_circ_106461,RMVar_hsa_circ_196563,RMVar_hsa_circ_122992,RMVar_hsa_circ_196565,RMVar_hsa_circ_196567,RMVar_hsa_circ_86699,RMVar_hsa_circ_115929,RMVar_hsa_circ_196566,RMVar_hsa_circ_196568,RMVar_hsa_circ_196569,RMVar_hsa_circ_110407,RMVar_hsa_circ_196571,RMVar_hsa_circ_339528,RMVar_hsa_circ_369820,RMVar_hsa_circ_196570 71044 RMVar_ID_71044 Human_SNP_ID_671024250 m1A Human chr19 - 58550541 58550541 58550541 TGGCCATGGGGGCTCCAGCCTCAGGGGCCATCACCAGGGCCACCAGACAGCTCCTGGGAACTCAG TGGCCATGGGGGCTCCAGCCTCAGGGGCCATCGCCAGGGCCACCAGACAGCTCCTGGGAACTCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58550491..58550660 26863196 MeRIP-seq:(Medium) rs779653197 Functional Loss SNV dbSNP153 33..33 33 - - - 71045 RMVar_ID_71045 Human_SNP_ID_671024272 m1A Human chr19 - 58550568 58550568 58550568 AGGACAGAGAACAGAGCCAGGCTGGGCTGGCCATGGGGGCTCCAGCCTCAGGGGCCATCACCAGG AGGACAGAGAACAGAGCCAGGCTGGGCTGGCCGTGGGGGCTCCAGCCTCAGGGGCCATCACCAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58550518..58550675 26863196 MeRIP-seq:(Medium) rs964693228 Functional Loss SNV dbSNP153 33..33 33 - - - 71046 RMVar_ID_71046 Human_SNP_ID_671024285 m1A Human chr19 - 58550591 58550590 58550592 CAGGGGAGTGGGGATGGGGTGACAGGACAGAGAACAGAGCCAGGCTGGGCTGGCCATGGGGGCTC CAGGGGAGTGGGGATGGGGTGACAGGACAGA__ACAGAGCCAGGCTGGGCTGGCCATGGGGGCTC TTC T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58550491..58550615 26863410 MeRIP-seq:(Medium) rs1415727749 Functional Loss DEL dbSNP153 32..33 33 - - - 71047 RMVar_ID_71047 Human_SNP_ID_671024290 m1A Human chr19 - 58550597 58550596 58550597 GGCCACCAGGGGAGTGGGGATGGGGTGACAGGACAGAGAACAGAGCCAGGCTGGGCTGGCCATGG GGCCACCAGGGGAGTGGGGATGGGGTGACAGG_CAGAGAACAGAGCCAGGCTGGGCTGGCCATGG GT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58550401..58550675 26863196 MeRIP-seq:(Medium) rs757521964 Functional Loss DEL dbSNP153 33..33 33 - - - 71048 RMVar_ID_71048 Human_SNP_ID_671024291 m1A Human chr19 - 58550597 58550597 58550597 GGCCACCAGGGGAGTGGGGATGGGGTGACAGGACAGAGAACAGAGCCAGGCTGGGCTGGCCATGG GGCCACCAGGGGAGTGGGGATGGGGTGACAGGGCAGAGAACAGAGCCAGGCTGGGCTGGCCATGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58550401..58550675 26863196 MeRIP-seq:(Medium) rs1202777563 Functional Loss SNV dbSNP153 33..33 33 - - - 71049 RMVar_ID_71049 Human_SNP_ID_671024927 m1A Human chr19 + 58552099 58552099 58552099 TCTTCCTCATCACCCATGGCATCATCAATGGCATCATTCATCATCTCCTCCTTCATATCCATGAT TCTTCCTCATCACCCATGGCATCATCAATGGCGTCATTCATCATCTCCTCCTTCATATCCATGAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58551961..58552385 26863196 MeRIP-seq:(Medium) rs564042865 Functional Loss SNV dbSNP153 33..33 33 - - - 71050 RMVar_ID_71050 Human_SNP_ID_671024930 m1A Human chr19 + 58552106 58552106 58552106 CATCACCCATGGCATCATCAATGGCATCATTCATCATCTCCTCCTTCATATCCATGATCTCTGCC CATCACCCATGGCATCATCAATGGCATCATTCTTCATCTCCTCCTTCATATCCATGATCTCTGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:58552055..58552266;chr19:58552004..58552255 26863196 MeRIP-seq:(Medium) rs1422972057 Functional Loss SNV dbSNP153 33..33 33 - - - 71051 RMVar_ID_71051 Human_SNP_ID_671025653 m1A Human chr19 - 58554124 58554124 58554124 GAGGGCCCTGAACCGTGCCATGCGGGAGCTGGACCGCGAGCGACAGAAACTAGAGACCCAGGAGA GAGGGCCCTGAACCGTGCCATGCGGGAGCTGGTCCGCGAGCGACAGAAACTAGAGACCCAGGAGA T A CHMP2A Ensembl:ENSG00000130724 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58554026..58554298;chr19:58554045..58554298 26863196 MeRIP-seq:(Medium) rs1365279794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558844,Human_RBP_ID_8840292,Human_RBP_ID_9381476,Human_RBP_ID_13527512,Human_RBP_ID_22449696,Human_RBP_ID_23114737,Human_RBP_ID_26336872,Human_RBP_ID_27815705 Human_Splice_Rec_2052309,Human_Splice_Rec_2052315,Human_Splice_Rec_2052325,Human_Splice_Rec_2052335,Human_Splice_Rec_2052345,Human_Splice_Rec_2052351 RMVar_hsa_circ_101179,RMVar_hsa_circ_196576,RMVar_hsa_circ_79905,RMVar_hsa_circ_196575,RMVar_hsa_circ_89704,RMVar_hsa_circ_196577 71052 RMVar_ID_71052 Human_SNP_ID_671026238 m1A Human chr19 - 58555821 58555821 58555821 TAGCCCCCCTGCTGGGTGCTTGTTCAGCCCCCACTCTGGGCTGTGGAGTGGGTGGGCAACGGGCC TAGCCCCCCTGCTGGGTGCTTGTTCAGCCCCCCCTCTGGGCTGTGGAGTGGGTGGGCAACGGGCC T G UBE2M Ensembl:ENSG00000130725 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58555776..58555955 26863196 MeRIP-seq:(Medium) rs1189782721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528597,Human_RBP_ID_771657,Human_RBP_ID_4574221,Human_RBP_ID_5117162,Human_RBP_ID_5145458,Human_RBP_ID_5239484,Human_RBP_ID_5374513,Human_RBP_ID_6792224,Human_RBP_ID_8256383,Human_RBP_ID_8838281,Human_RBP_ID_13527575,Human_RBP_ID_17655396,Human_RBP_ID_17933326,Human_RBP_ID_18192559,Human_RBP_ID_22592711,Human_RBP_ID_23211399,Human_RBP_ID_24485122,Human_RBP_ID_26472944,Human_RBP_ID_26770109,Human_RBP_ID_26996858,Human_RBP_ID_27279655 Human_miRNA_ID_1419522 RMVar_hsa_circ_104758,RMVar_hsa_circ_121441,RMVar_hsa_circ_108775,RMVar_hsa_circ_196580,RMVar_hsa_circ_196582,RMVar_hsa_circ_99180,RMVar_hsa_circ_196581,RMVar_hsa_circ_196579 71053 RMVar_ID_71053 Human_SNP_ID_671026370 m1A Human chr19 - 58556077 58556077 58556077 TTTGAGCGCTGCCTGAAATAGGGTTGGCGCATACCCACCCCCGCCACGGCCACAAGCCCTGGCAT TTTGAGCGCTGCCTGAAATAGGGTTGGCGCATCCCCACCCCCGCCACGGCCACAAGCCCTGGCAT T G UBE2M Ensembl:ENSG00000130725 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58556026..58556323 26863196 MeRIP-seq:(Medium) rs757763772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528602,Human_RBP_ID_4574229,Human_RBP_ID_5238925,Human_RBP_ID_8496070,Human_RBP_ID_17656424,Human_RBP_ID_25437619,Human_RBP_ID_27473692 Human_miRNA_ID_2027664,Human_miRNA_ID_2147497,Human_miRNA_ID_2988923,Human_miRNA_ID_3022626 RMVar_hsa_circ_104758,RMVar_hsa_circ_121441,RMVar_hsa_circ_108775,RMVar_hsa_circ_196580,RMVar_hsa_circ_196582,RMVar_hsa_circ_99180,RMVar_hsa_circ_196581,RMVar_hsa_circ_196579 71054 RMVar_ID_71054 Human_SNP_ID_671026481 m1A Human chr19 - 58556377 58556377 58556377 AGCCCTGACCCTGATGCTCTCTGTCCACAGAGAGGACTGGAAGCCAGTCCTTACGATAAACTCCA AGCCCTGACCCTGATGCTCTCTGTCCACAGAGTGGACTGGAAGCCAGTCCTTACGATAAACTCCA T A UBE2M Ensembl:ENSG00000130725 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58556301..58556400 32194978 MeRIP-seq:(Medium) rs111247680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54012,Human_RBP_ID_528606,Human_RBP_ID_1573931,Human_RBP_ID_2571760,Human_RBP_ID_22666940,Human_RBP_ID_26816414 Human_Splice_Rec_2052364,Human_Splice_Rec_2052365,Human_Splice_Rec_2052374,Human_Splice_Rec_2052375,Human_Splice_Rec_2052382 RMVar_hsa_circ_104758,RMVar_hsa_circ_121441,RMVar_hsa_circ_108775,RMVar_hsa_circ_196580,RMVar_hsa_circ_196582,RMVar_hsa_circ_196581 71055 RMVar_ID_71055 Human_SNP_ID_671026702 m1A Human chr19 + 58557049 58557049 58557049 GACACCCTTGGTTTGCTCCTGGGAATTCAGCCATATGCACCCTCACCTCATCAGGACAGATGACC GACACCCTTGGTTTGCTCCTGGGAATTCAGCCGTATGCACCCTCACCTCATCAGGACAGATGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58557046..58557121 26863196 MeRIP-seq:(Medium) rs756543563 Functional Loss SNV dbSNP153 33..33 33 - - - 71056 RMVar_ID_71056 Human_SNP_ID_671027122 m1A Human chr19 - 58558324 58558324 58558324 AGCAGAAGAAGGAGGAGGAGTCGGCGGGCGGCACCAAGGGCAGCAGCAAGAAGGCGTCGGCGGCG AGCAGAAGAAGGAGGAGGAGTCGGCGGGCGGCTCCAAGGGCAGCAGCAAGAAGGCGTCGGCGGCG T A UBE2M Ensembl:ENSG00000130725 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58557152..58558475 32194978 MeRIP-seq:(Medium) rs758822206 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4574239,Human_RBP_ID_6792247,Human_RBP_ID_9347051,Human_RBP_ID_22812769,Human_RBP_ID_23131894,Human_RBP_ID_26336875,Human_RBP_ID_26996873,Human_RBP_ID_27815708 Human_Splice_Rec_2052357,Human_Splice_Rec_2052367 RMVar_hsa_circ_104758,RMVar_hsa_circ_196582 71057 RMVar_ID_71057 Human_SNP_ID_671027185 m1A Human chr19 + 58558433 58558433 58558433 CTGCCGCCGCCGCGGGGCCCGGGACCCCGGCCACCCGGCCCCCCGCCGCCGCCCGCGTCGCCTCC CTGCCGCCGCCGCGGGGCCCGGGACCCCGGCCCCCCGGCCCCCCGCCGCCGCCCGCGTCGCCTCC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr19:58558276..58558614;chr19:58558316..58558663 26863410 MeRIP-seq:(Medium) rs1366098055 Functional Loss SNV dbSNP153 33..33 33 - - - 71058 RMVar_ID_71058 Human_SNP_ID_671027203 m1A Human chr19 - 58558491 58558488 58558491 GCAGGCCGGGCGGGTGGCGGCAGCAGCGGAGGAGGCCGCAGCTGCGGGTCCGAGGAGCGGAGGCG GCAGGCCGGGCGGGTGGCGGCAGCAGCGGAGG___CCGCAGCTGCGGGTCCGAGGAGCGGAGGCG GCCT G UBE2M Ensembl:ENSG00000130725 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr19:58558251..58558925;chr19:58558251..58558950;chr19:58558301..58558700 26863196 MeRIP-seq:(Medium) rs966368192 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_771663,Human_RBP_ID_914162,Human_RBP_ID_4552606,Human_RBP_ID_5321964,Human_RBP_ID_8728456,Human_RBP_ID_8942249,Human_RBP_ID_9329257,Human_RBP_ID_9353773,Human_RBP_ID_18470686,Human_RBP_ID_22533518,Human_RBP_ID_26336876,Human_RBP_ID_27815709 RMVar_hsa_circ_104758,RMVar_hsa_circ_196582 71059 RMVar_ID_71059 Human_SNP_ID_671027289 m1A Human chr19 - 58558709 58558709 58558709 GCCCCGAGTCCGCAGCTGCAGCGGGGCCTGAGACCAGAGTTGGCGAGGGCAAGGAAGGAGCGGCC GCCCCGAGTCCGCAGCTGCAGCGGGGCCTGAGGCCAGAGTTGGCGAGGGCAAGGAAGGAGCGGCC T C UBE2M Ensembl:ENSG00000130725 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58558514..58558884 32194978 MeRIP-seq:(Medium) rs1042133866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4552617 RMVar_hsa_circ_104758,RMVar_hsa_circ_196582 71060 RMVar_ID_71060 Human_SNP_ID_671027371 m1A Human chr19 - 58558876 58558876 58558876 GGCGCCCGAGGCCGTTGCCGACCTCCGCGCTAAAGCCGCTGCTGCCGCGGAAGACGATCCTCCAG GGCGCCCGAGGCCGTTGCCGACCTCCGCGCTAGAGCCGCTGCTGCCGCGGAAGACGATCCTCCAG T C UBE2M Ensembl:ENSG00000130725 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58557101..58558975 26863410 MeRIP-seq:(Medium) rs893278988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528610,Human_RBP_ID_4552633,Human_RBP_ID_26996875 Human_miRNA_ID_2757196 RMVar_hsa_circ_104758,RMVar_hsa_circ_196582 71061 RMVar_ID_71061 Human_SNP_ID_671027372 m1A Human chr19 - 58558876 58558876 58558876 GGCGCCCGAGGCCGTTGCCGACCTCCGCGCTAAAGCCGCTGCTGCCGCGGAAGACGATCCTCCAG GGCGCCCGAGGCCGTTGCCGACCTCCGCGCTACAGCCGCTGCTGCCGCGGAAGACGATCCTCCAG T G UBE2M Ensembl:ENSG00000130725 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:58557101..58558975 26863410 MeRIP-seq:(Medium) rs893278988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528610,Human_RBP_ID_4552633,Human_RBP_ID_26996875 Human_miRNA_ID_2757196 RMVar_hsa_circ_104758,RMVar_hsa_circ_196582 71062 RMVar_ID_71062 Human_SNP_ID_671027376 m1A Human chr19 + 58558893 58558893 58558893 GCGGCAGCAGCGGCTTTAGCGCGGAGGTCGGCAACGGCCTCGGGCGCCCCGCCGCTTCGGATATT GCGGCAGCAGCGGCTTTAGCGCGGAGGTCGGCGACGGCCTCGGGCGCCCCGCCGCTTCGGATATT A G lnc-TRIM28-13 RNACentral:URS0000D580B5 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:58558810..58558898 26863410 MeRIP-seq:(Medium) rs1053485359 Functional Loss SNV dbSNP153 33..33 33 - - - 71063 RMVar_ID_71063 Human_SNP_ID_671032566 m1A Human chr19 + 58573774 58573772 58573775 GGGCAGAGAGATGCCGATCGATAGAAACAGCGAGGAGAGACGGAGAGAGACCAGAGACTCAAGGG GGGCAGAGAGATGCCGATCGATAGAAACAGC___GAGAGACGGAGAGAGACCAGAGACTCAAGGG CGAG C MZF1-AS1,CENPBD1P1 Ensembl:ENSG00000267858,Ensembl:ENSG00000213753 lincRNA,Pseudogene exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58573724..58574007 26863196 MeRIP-seq:(Medium) rs977389069 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5088855,Human_RBP_ID_5586017 71064 RMVar_ID_71064 Human_SNP_ID_671032574 m1A Human chr19 + 58573802 58573802 58573802 AGCGAGGAGAGACGGAGAGAGACCAGAGACTCAAGGGCAAAGAGAGACGAAGGACCGGCGGGAGG AGCGAGGAGAGACGGAGAGAGACCAGAGACTCGAGGGCAAAGAGAGACGAAGGACCGGCGGGAGG A G MZF1-AS1,CENPBD1P1 Ensembl:ENSG00000267858,Ensembl:ENSG00000213753 lincRNA,Pseudogene exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58573752..58573972 26863196 MeRIP-seq:(Medium) rs1289814786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824308 71065 RMVar_ID_71065 Human_SNP_ID_671035563 m1A Human chr19 + 58584115 58584115 58584115 CCTGTAATCTCAGCACTTTAGGAGGCTGAGGCAGGAGGATAGCTTGAGGCCAGGAGTTCGAGACT CCTGTAATCTCAGCACTTTAGGAGGCTGAGGCGGGAGGATAGCTTGAGGCCAGGAGTTCGAGACT A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1133048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9929775,Human_RBP_ID_17387616 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 71066 RMVar_ID_71066 Human_SNP_ID_671037641 m1A Human chr19 + 58591311 58591311 58591311 GTAAAGATAATAATAGGGTTAGGCATAGGATTAGGATCTGGGTCAGAGTCAGGGCTGGAAGTATG GTAAAGATAATAATAGGGTTAGGCATAGGATTGGGATCTGGGTCAGAGTCAGGGCTGGAAGTATG A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58591309..58591405 26863196 MeRIP-seq:(Medium) rs978118771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5586069,Human_RBP_ID_6792358 71067 RMVar_ID_71067 Human_SNP_ID_26751210 m1A Human chr1 - 107056746 107056746 107056746 AGTTCCCTCCCCTCCTTCGCCGCCGCCCCCCGACTCAAGCTTTCTTTTCTTGGGCTGCGACATCT AGTTCCCTCCCCTCCTTCGCCGCCGCCCCCCGCCTCAAGCTTTCTTTTCTTGGGCTGCGACATCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:107056701..107056926 26863196 MeRIP-seq:(Medium) rs1428101771 Functional Loss SNV dbSNP153 33..33 33 - - - 71068 RMVar_ID_71068 Human_SNP_ID_26751390 m1A Human chr1 - 107057101 107057101 107057101 CTGGTCCCGGCAGGACGTGCACCCGGTCCTCCAGCCCGTTGAACCGCACCACCTCCCGGGCCTGT CTGGTCCCGGCAGGACGTGCACCCGGTCCTCCGGCCCGTTGAACCGCACCACCTCCCGGGCCTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:107057023..107057123 26863196 MeRIP-seq:(Medium) rs1350712067 Functional Loss SNV dbSNP153 33..33 33 - - - 71069 RMVar_ID_71069 Human_SNP_ID_26751739 m1A Human chr1 + 107057801 107057801 107057801 CGCCTGCGCGTGCTGCTGCGCTACAAAGTGGGAGACCAGGAGGAGAAGACCAAAGACTTTGCCAT CGCCTGCGCGTGCTGCTGCGCTACAAAGTGGGGGACCAGGAGGAGAAGACCAAAGACTTTGCCAT A G PRMT6 Ensembl:ENSG00000198890 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:107057576..107057863 26863196 MeRIP-seq:(Medium) rs990057019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664557,Human_RBP_ID_8731925 71070 RMVar_ID_71070 Human_SNP_ID_26858158 m1A Human chr1 + 107505306 107505306 107505306 TGGAGCTTCTGGAGCAACACTGTATCTCTTGCATCTGGCATTGTTCAATCCAGATGTTTGTTGGG TGGAGCTTCTGGAGCAACACTGTATCTCTTGCGTCTGGCATTGTTCAATCCAGATGTTTGTTGGG A G AC114491.1 Ensembl:ENSG00000224550 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs529972278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22778750,Human_RBP_ID_26389489,Human_RBP_ID_26836494 71071 RMVar_ID_71071 Human_SNP_ID_26874019 m1A Human chr1 - 107570887 107570881 107570888 GCCGCAGGTGCAGATGTTGGTGGTAGTAGCACATATTCTAAAGAGAACTTCAAAGGCCGAAGTGG GCCGCAGGTGCAGATGTTGGTGGTAGTAGCA_______TAAAGAGAACTTCAAAGGCCGAAGTGG AGAATATG A RF02543-002 RNACentral:URS000097CDD0 rRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:107570837..107570994 26863196 MeRIP-seq:(Medium) rs1449563291 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_1122089,Human_RBP_ID_1148482,Human_RBP_ID_2179890,Human_RBP_ID_3979562,Human_RBP_ID_5155573,Human_RBP_ID_5432574,Human_RBP_ID_5455939,Human_RBP_ID_5483896,Human_RBP_ID_5664653,Human_RBP_ID_8279731,Human_RBP_ID_8731933,Human_RBP_ID_8953285,Human_RBP_ID_9446552,Human_RBP_ID_10501640,Human_RBP_ID_16979160,Human_RBP_ID_17210897,Human_RBP_ID_17328954,Human_RBP_ID_17444387,Human_RBP_ID_17674368,Human_RBP_ID_17719999,Human_RBP_ID_18428126,Human_RBP_ID_18546470,Human_RBP_ID_19151051,Human_RBP_ID_22778756,Human_RBP_ID_22872219,Human_RBP_ID_23143060,Human_RBP_ID_23320086,Human_RBP_ID_24749722,Human_RBP_ID_26364913,Human_RBP_ID_26576431,Human_RBP_ID_27152644,Human_RBP_ID_27385266,Human_RBP_ID_27554109,Human_RBP_ID_27575521 71072 RMVar_ID_71072 Human_SNP_ID_26876277 m1A Human chr1 - 107579784 107579782 107579784 GTGGAAATGGATGCAGATTTCATTAGAGAGACAAGAGTGGCCAGATTATGAATTGTCATGGAATT GTGGAAATGGATGCAGATTTCATTAGAGAGAC__GAGTGGCCAGATTATGAATTGTCATGGAATT CTT C VAV3 Ensembl:ENSG00000134215 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:107579781..107579944 26863196 MeRIP-seq:(Medium) rs1186249206 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_125859,RMVar_hsa_circ_34115,RMVar_hsa_circ_135026 71073 RMVar_ID_71073 Human_SNP_ID_27024365 m1A Human chr1 - 108200049 108200049 108200049 CAGCCGACGCGCTACGAGACCCTCTTCCAGGCACTGGACCGCAATGGGGACGGAGTGGTGGACAT CAGCCGACGCGCTACGAGACCCTCTTCCAGGCCCTGGACCGCAATGGGGACGGAGTGGTGGACAT T G SLC25A24 Ensembl:ENSG00000085491 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:108200001..108200200 26863196 MeRIP-seq:(Medium) rs373391768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319644,Human_RBP_ID_4074219,Human_RBP_ID_8731945,Human_RBP_ID_9270224,Human_RBP_ID_18546497 Human_Splice_Rec_104063,Human_Splice_Rec_104081,Human_Splice_Rec_104115 71074 RMVar_ID_71074 Human_SNP_ID_27024398 m1A Human chr1 - 108200105 108200105 108200105 TGTTGCGCTGGCTGCGGGACTTCGTGCTGCCCACCGCGGCCTGCCAGGACGCGGAGCAGCCGACG TGTTGCGCTGGCTGCGGGACTTCGTGCTGCCCTCCGCGGCCTGCCAGGACGCGGAGCAGCCGACG T A SLC25A24 Ensembl:ENSG00000085491 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:108200054..108200326;chr1:108200057..108200317 26863196 MeRIP-seq:(Medium) rs763318894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072950,Human_RBP_ID_8754045,Human_RBP_ID_9270225,Human_RBP_ID_9319045 71075 RMVar_ID_71075 Human_SNP_ID_27024470 m1A Human chr1 - 108200252 108200252 108200252 GCGCCGCAGCCGCAACCCCGACGGCGCCCCAAACGCTGTTGCGCCGCGCGCCCCGCCCAGCCCGG GCGCCGCAGCCGCAACCCCGACGGCGCCCCAATCGCTGTTGCGCCGCGCGCCCCGCCCAGCCCGG T A SLC25A24 Ensembl:ENSG00000085491 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:108200157..108200358 26863410 MeRIP-seq:(Medium) rs888195329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074220 71076 RMVar_ID_71076 Human_SNP_ID_27024471 m1A Human chr1 - 108200252 108200252 108200252 GCGCCGCAGCCGCAACCCCGACGGCGCCCCAAACGCTGTTGCGCCGCGCGCCCCGCCCAGCCCGG GCGCCGCAGCCGCAACCCCGACGGCGCCCCAAGCGCTGTTGCGCCGCGCGCCCCGCCCAGCCCGG T C SLC25A24 Ensembl:ENSG00000085491 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:108200157..108200358 26863410 MeRIP-seq:(Medium) rs888195329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074220 71077 RMVar_ID_71077 Human_SNP_ID_27083512 m1A Human chr1 + 108560122 108560107 108560122 CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CCCGACTCCCAGACGGGC_______________GGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CGGCAGCGGCGGCGGA C FAM102B Ensembl:ENSG00000162636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108560058..108560195 26863196 MeRIP-seq:(Medium) rs1483206813 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_4074221,Human_RBP_ID_9270226 71078 RMVar_ID_71078 Human_SNP_ID_27083516 m1A Human chr1 + 108560122 108560110 108560122 CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CCCGACTCCCAGACGGGCGGC____________GGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CAGCGGCGGCGGA C FAM102B Ensembl:ENSG00000162636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108560058..108560195 26863196 MeRIP-seq:(Medium) rs1232375475 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4074221,Human_RBP_ID_9270226 71079 RMVar_ID_71079 Human_SNP_ID_27083529 m1A Human chr1 + 108560122 108560111 108560123 CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CCCGACTCCCAGACGGGCGGCA____________GCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC AGCGGCGGCGGAG A FAM102B Ensembl:ENSG00000162636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108560058..108560195 26863196 MeRIP-seq:(Medium) rs1468738872 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_4074221,Human_RBP_ID_9270226 71080 RMVar_ID_71080 Human_SNP_ID_27083534 m1A Human chr1 + 108560122 108560113 108560122 CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CCCGACTCCCAGACGGGCGGCAGC_________GGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CGGCGGCGGA C FAM102B Ensembl:ENSG00000162636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108560058..108560195 26863196 MeRIP-seq:(Medium) rs1251244750 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4074221,Human_RBP_ID_9270226 71081 RMVar_ID_71081 Human_SNP_ID_27083540 m1A Human chr1 + 108560122 108560122 108560122 CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC CCCGACTCCCAGACGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGAGCTGAGCAC A C FAM102B Ensembl:ENSG00000162636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108560058..108560195 26863196 MeRIP-seq:(Medium) rs867010869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074221,Human_RBP_ID_9270226 71082 RMVar_ID_71082 Human_SNP_ID_27090760 m1A Human chr1 - 108591754 108591754 108591754 TTGTCATTACCTCCTCTAGAAATCTCTCTGCAACTCGGTGTCCCATATGACCAGGCCTGCCTTGG TTGTCATTACCTCCTCTAGAAATCTCTCTGCAGCTCGGTGTCCCATATGACCAGGCCTGCCTTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:108591744..108591927 26863196 MeRIP-seq:(Medium) rs553258186 Functional Loss SNV dbSNP153 33..33 33 - - - 71083 RMVar_ID_71083 Human_SNP_ID_27107363 m1A Human chr1 - 108661049 108661049 108661049 GGCGCTGAGTTGAGGACGCTGGCGGCTCCGCGACGAGCTTTGTTTTTTCGGTTGGGCATGCTGCT GGCGCTGAGTTGAGGACGCTGGCGGCTCCGCGGCGAGCTTTGTTTTTTCGGTTGGGCATGCTGCT T C HENMT1 Ensembl:ENSG00000162639 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:108660939..108661250 26863196 MeRIP-seq:(Medium) rs1245768935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_104371,Human_Splice_Rec_104385,Human_Splice_Rec_104401,Human_Splice_Rec_104429,Human_Splice_Rec_104443 RMVar_hsa_circ_117077,RMVar_hsa_circ_135053 71084 RMVar_ID_71084 Human_SNP_ID_27115352 m1A Human chr1 - 108692405 108692405 108692405 CGACGCCGACAAAATGACCCCGGGCCAAGAGCAGACAGCGAAACCCAGACCGCGAGAACTCCACG CGACGCCGACAAAATGACCCCGGGCCAAGAGCTGACAGCGAAACCCAGACCGCGAGAACTCCACG T A lnc-HENMT1-2,lnc-HENMT1-2:2 RNACentral:URS0000D5BD78,RNACentral:URS00008BB576 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:108692354..108692621 26863196 MeRIP-seq:(Medium) rs942515854 Functional Loss SNV dbSNP153 33..33 33 - - - 71085 RMVar_ID_71085 Human_SNP_ID_27144583 m1A Human chr1 + 108808879 108808879 108808879 GGATAAAGTCTCCTTAATTAAAGATGAATAGCATTTCTTTTTGGAGGGTTTAGAGATTCTTACTA GGATAAAGTCTCCTTAATTAAAGATGAATAGCCTTTCTTTTTGGAGGGTTTAGAGATTCTTACTA A C STXBP3 Ensembl:ENSG00000116266 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1149154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_104578 71086 RMVar_ID_71086 Human_SNP_ID_27144584 m1A Human chr1 + 108808879 108808879 108808879 GGATAAAGTCTCCTTAATTAAAGATGAATAGCATTTCTTTTTGGAGGGTTTAGAGATTCTTACTA GGATAAAGTCTCCTTAATTAAAGATGAATAGCGTTTCTTTTTGGAGGGTTTAGAGATTCTTACTA A G STXBP3 Ensembl:ENSG00000116266 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1149154 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_104578 71087 RMVar_ID_71087 Human_SNP_ID_27144585 m1A Human chr1 + 108808879 108808879 108808879 GGATAAAGTCTCCTTAATTAAAGATGAATAGCATTTCTTTTTGGAGGGTTTAGAGATTCTTACTA GGATAAAGTCTCCTTAATTAAAGATGAATAGCTTTTCTTTTTGGAGGGTTTAGAGATTCTTACTA A T STXBP3 Ensembl:ENSG00000116266 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1149154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_104578 71088 RMVar_ID_71088 Human_SNP_ID_27161399 m1A Human chr1 + 108877102 108877089 108877102 AGCTCTGGCCCACGTGACCTGCCGGGGGCGGGAGCAGGGGGCGCGCCGGCCTCCTGCGGTGCCCC AGCTCTGGCCCACGTGACCT_____________GCAGGGGGCGCGCCGGCCTCCTGCGGTGCCCC TGCCGGGGGCGGGA T GPSM2 Ensembl:ENSG00000121957 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:108877051..108877257 26863196 MeRIP-seq:(Medium) rs1187136549 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_4072952 71089 RMVar_ID_71089 Human_SNP_ID_27178511 m1A Human chr1 + 108949102 108949102 108949102 AAGCCATCAACATTTGCCTATTCTACCTCATAAAAGTTTAATATCTGCCTCTTATCTTCAACCCA AAGCCATCAACATTTGCCTATTCTACCTCATAGAAGTTTAATATCTGCCTCTTATCTTCAACCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108949100..108949264 26863196 MeRIP-seq:(Medium) rs1248876989 Functional Loss SNV dbSNP153 33..33 33 - - - 71090 RMVar_ID_71090 Human_SNP_ID_27182127 m1A Human chr1 - 108963422 108963422 108963422 CGCTGAAACCCTGGGCGGCGGCAAGCTGTGCGACCTCTTCTGCGGCCGGCCTGGGCAGGTGTCTT CGCTGAAACCCTGGGCGGCGGCAAGCTGTGCGGCCTCTTCTGCGGCCGGCCTGGGCAGGTGTCTT T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:108963253..108963434 26863196 MeRIP-seq:(Medium) rs746245787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319985,Human_RBP_ID_4074229,Human_RBP_ID_5455952,Human_RBP_ID_5483914,Human_RBP_ID_22023588 Human_Splice_Rec_104757,Human_Splice_Rec_104955,Human_Splice_Rec_104979 71091 RMVar_ID_71091 Human_SNP_ID_27182132 m1A Human chr1 + 108963428 108963428 108963428 CCTGCCCAGGCCGGCCGCAGAAGAGGTCGCACAGCTTGCCGCCGCCCAGGGTTTCAGCGTGCTTC CCTGCCCAGGCCGGCCGCAGAAGAGGTCGCACGGCTTGCCGCCGCCCAGGGTTTCAGCGTGCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:108963252..108963484 26863196 MeRIP-seq:(Medium) rs1222111532 Functional Loss SNV dbSNP153 33..33 33 - - - 71092 RMVar_ID_71092 Human_SNP_ID_27184238 m1A Human chr1 + 108972277 108972277 108972277 AACAAAATATATCTCAAATTTAGTCATTTCTTACTACCTCCACCTCCACCACCCTAGTCCAAGCC AACAAAATATATCTCAAATTTAGTCATTTCTTTCTACCTCCACCTCCACCACCCTAGTCCAAGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:108972257..108972323 26863196 MeRIP-seq:(Medium) rs959868420 Functional Loss SNV dbSNP153 33..33 33 - - - 71093 RMVar_ID_71093 Human_SNP_ID_27201815 m1A Human chr1 + 109042050 109042050 109042050 TCAATCCATCAGTTCGTCAATCCGTCCTTCTCACGTCCGCCCCTCCCGGCCCAGCGACTCCTCAG TCAATCCATCAGTTCGTCAATCCGTCCTTCTCCCGTCCGCCCCTCCCGGCCCAGCGACTCCTCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109041893..109042113 26863196 MeRIP-seq:(Medium) rs1213061991 Functional Loss SNV dbSNP153 33..33 33 - - - 71094 RMVar_ID_71094 Human_SNP_ID_27207719 m1A Human chr1 - 109064035 109064035 109064035 TCCTTCCTCAGCCTCTCGAGTAGCTGGGAAGTACAGGCGCCTGCCACCACGCCTGGCTAACTTTT TCCTTCCTCAGCCTCTCGAGTAGCTGGGAAGTGCAGGCGCCTGCCACCACGCCTGGCTAACTTTT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1035289010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26386202 71095 RMVar_ID_71095 Human_SNP_ID_27215417 m1A Human chr1 + 109090826 109090826 109090826 TGTCAAGCGGGCGCTCCCCCATCTCCGCCGCTATTACCACTGAACCCGGACCCCCTACCCAGGTC TGTCAAGCGGGCGCTCCCCCATCTCCGCCGCTGTTACCACTGAACCCGGACCCCCTACCCAGGTC A G TMEM167B Ensembl:ENSG00000215717 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:109090729..109090872 26863196 MeRIP-seq:(Medium) rs751886583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3980098,Human_RBP_ID_5432584,Human_RBP_ID_5455955,Human_RBP_ID_18415017,Human_RBP_ID_22778784,Human_RBP_ID_26798606,Human_RBP_ID_27385328 Human_Splice_Rec_105219,Human_Splice_Rec_105223,Human_Splice_Rec_105227,Human_Splice_Rec_105233 RMVar_hsa_circ_108740,RMVar_hsa_circ_135136 71096 RMVar_ID_71096 Human_SNP_ID_27215443 m1A Human chr1 + 109090873 109090873 109090873 GGACCCCCTACCCAGGTCCAGGGCCAGCCGCCATGACGAACGGTGAGAACTGATGCCCTGAGCGG GGACCCCCTACCCAGGTCCAGGGCCAGCCGCCCTGACGAACGGTGAGAACTGATGCCCTGAGCGG A C TMEM167B Ensembl:ENSG00000215717 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:109090783..109090875 26863410 MeRIP-seq:(Medium) rs1349055766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074230,Human_RBP_ID_26798607 Human_Splice_Rec_105219,Human_Splice_Rec_105223,Human_Splice_Rec_105227,Human_Splice_Rec_105233 RMVar_hsa_circ_108740,RMVar_hsa_circ_135136 71097 RMVar_ID_71097 Human_SNP_ID_27217906 m1A Human chr1 - 109100253 109100251 109100253 GTCCACTCACACTCACCCTGCACGCGCCTCACACGCGACGCCACAGCTCCGCACACAACACCCAG GTCCACTCACACTCACCCTGCACGCGCCTCAC__GCGACGCCACAGCTCCGCACACAACACCCAG CGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:109100176..109100539;chr1:109100166..109100546;chr1:109100151..109100575;chr1:109100171..109100450;chr1:109100176..109100575;chr1:109100145..109100525 26863196 MeRIP-seq:(Medium) rs1557997080 Functional Loss DEL dbSNP153 33..34 33 - - - 71098 RMVar_ID_71098 Human_SNP_ID_27217943 m1A Human chr1 - 109100303 109100303 109100303 GCACGCACTCGCCTAACACGCTCCAAGCGCGCACACTCACACACTCACGCGTCCACTCACACTCA GCACGCACTCGCCTAACACGCTCCAAGCGCGCGCACTCACACACTCACGCGTCCACTCACACTCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:109100126..109100516 26863196 MeRIP-seq:(Medium) rs1402504376 Functional Loss SNV dbSNP153 33..33 33 - - - 71099 RMVar_ID_71099 Human_SNP_ID_27246596 m1A Human chr1 - 109213945 109213945 109213945 GCCAACGCTCAGGGAAGCAAGGATCGCGCCGCAGCACTCAGCCTGTGACCGCCGCACTGCGCCGG GCCAACGCTCAGGGAAGCAAGGATCGCGCCGCCGCACTCAGCCTGTGACCGCCGCACTGCGCCGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109213926..109213950 32194978 MeRIP-seq:(Medium) rs1275790954 Functional Loss SNV dbSNP153 33..33 33 - - - 71100 RMVar_ID_71100 Human_SNP_ID_27246642 m1A Human chr1 + 109214028 109214028 109214028 GTGCTGGATCTGGATTTGTTTCGGGTGGATAAAGGAGGGGACCCAGCCCTCATCCGAGAGACGCA GTGCTGGATCTGGATTTGTTTCGGGTGGATAACGGAGGGGACCCAGCCCTCATCCGAGAGACGCA A C SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:109213901..109214162;chr1:109213901..109214193 26863196 MeRIP-seq:(Medium) rs956299438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16834,Human_RBP_ID_741350,Human_RBP_ID_800911,Human_RBP_ID_1148538,Human_RBP_ID_1407511,Human_RBP_ID_1721408,Human_RBP_ID_3980146,Human_RBP_ID_5666020,Human_RBP_ID_17720268,Human_RBP_ID_18428153,Human_RBP_ID_22023592,Human_RBP_ID_22430705,Human_RBP_ID_22870904,Human_RBP_ID_23320864,Human_RBP_ID_26311575,Human_RBP_ID_27800593 RMVar_hsa_circ_99789,RMVar_hsa_circ_135146 71101 RMVar_ID_71101 Human_SNP_ID_27246649 m1A Human chr1 + 109214075 109214075 109214075 CCTCATCCGAGAGACGCAGGAGAAGCGCTTCAAGGACCCGGGACTAGTGGACCAGCTGGTGAAGG CCTCATCCGAGAGACGCAGGAGAAGCGCTTCAGGGACCCGGGACTAGTGGACCAGCTGGTGAAGG A G SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr1:109213901..109214150;chr1:109214026..109214150 26863196,32194978 MeRIP-seq:(Medium) rs922326709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16834,Human_RBP_ID_273301,Human_RBP_ID_801452,Human_RBP_ID_1407513,Human_RBP_ID_1721409,Human_RBP_ID_3275560,Human_RBP_ID_3980147,Human_RBP_ID_5536224,Human_RBP_ID_5666021,Human_RBP_ID_8280099,Human_RBP_ID_8732088,Human_RBP_ID_9359107,Human_RBP_ID_10506121,Human_RBP_ID_18546673,Human_RBP_ID_22025169,Human_RBP_ID_22430705,Human_RBP_ID_22485385,Human_RBP_ID_22870904,Human_RBP_ID_23320866,Human_RBP_ID_26311576,Human_RBP_ID_26365256,Human_RBP_ID_26836687,Human_RBP_ID_27800594 Human_Splice_Rec_105535,Human_Splice_Rec_105555,Human_Splice_Rec_105557,Human_Splice_Rec_105565 RMVar_hsa_circ_99789,RMVar_hsa_circ_135146 71102 RMVar_ID_71102 Human_SNP_ID_27246658 m1A Human chr1 + 109214096 109214096 109214096 GAAGCGCTTCAAGGACCCGGGACTAGTGGACCAGCTGGTGAAGGCAGACAGCGAGTGGCGACGAT GAAGCGCTTCAAGGACCCGGGACTAGTGGACCGGCTGGTGAAGGCAGACAGCGAGTGGCGACGAT A G SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:109213976..109214150 26863196 MeRIP-seq:(Medium) rs373847424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16834,Human_RBP_ID_220991,Human_RBP_ID_273301,Human_RBP_ID_801452,Human_RBP_ID_1407513,Human_RBP_ID_1721409,Human_RBP_ID_3275560,Human_RBP_ID_5536224,Human_RBP_ID_5666021,Human_RBP_ID_8280101,Human_RBP_ID_8732089,Human_RBP_ID_9359107,Human_RBP_ID_10506121,Human_RBP_ID_18428154,Human_RBP_ID_22025169,Human_RBP_ID_22427341,Human_RBP_ID_22870905,Human_RBP_ID_23320866,Human_RBP_ID_26311576,Human_RBP_ID_26836687,Human_RBP_ID_27800594 Human_Splice_Rec_105535,Human_Splice_Rec_105555,Human_Splice_Rec_105557,Human_Splice_Rec_105565 Human_miRNA_ID_2454851 RMVar_hsa_circ_99789,RMVar_hsa_circ_135146 71103 RMVar_ID_71103 Human_SNP_ID_27246659 m1A Human chr1 + 109214096 109214096 109214096 GAAGCGCTTCAAGGACCCGGGACTAGTGGACCAGCTGGTGAAGGCAGACAGCGAGTGGCGACGAT GAAGCGCTTCAAGGACCCGGGACTAGTGGACCTGCTGGTGAAGGCAGACAGCGAGTGGCGACGAT A T SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:109213976..109214150 26863196 MeRIP-seq:(Medium) rs373847424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16834,Human_RBP_ID_220991,Human_RBP_ID_273301,Human_RBP_ID_801452,Human_RBP_ID_1407513,Human_RBP_ID_1721409,Human_RBP_ID_3275560,Human_RBP_ID_5536224,Human_RBP_ID_5666021,Human_RBP_ID_8280101,Human_RBP_ID_8732089,Human_RBP_ID_9359107,Human_RBP_ID_10506121,Human_RBP_ID_18428154,Human_RBP_ID_22025169,Human_RBP_ID_22427341,Human_RBP_ID_22870905,Human_RBP_ID_23320866,Human_RBP_ID_26311576,Human_RBP_ID_26836687,Human_RBP_ID_27800594 Human_Splice_Rec_105535,Human_Splice_Rec_105555,Human_Splice_Rec_105557,Human_Splice_Rec_105565 Human_miRNA_ID_2454851 RMVar_hsa_circ_99789,RMVar_hsa_circ_135146 71104 RMVar_ID_71104 Human_SNP_ID_27250502 m1A Human chr1 - 109228375 109228375 109228375 TCGAAACTCAGCACATTCTCTGGGACAGACTCATCATCTCCCACTGGCTCTTTTTTCTGCAGGAA TCGAAACTCAGCACATTCTCTGGGACAGACTCGTCATCTCCCACTGGCTCTTTTTTCTGCAGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:109228351..109228375;chr1:109228351..109228450 26863196 MeRIP-seq:(Medium) rs1300012434 Functional Loss SNV dbSNP153 33..33 33 - - - 71105 RMVar_ID_71105 Human_SNP_ID_27251131 m1A Human chr1 - 109230964 109230964 109230964 GCCACCACGGCCCCCTTTTCGCCTTCAAAGCCATCTACCATCACCACCAGGTCCACATGAGAGTA GCCACCACGGCCCCCTTTTCGCCTTCAAAGCCGTCTACCATCACCACCAGGTCCACATGAGAGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109230835..109231046 26863196 MeRIP-seq:(Medium) rs140305400 Functional Loss SNV dbSNP153 33..33 33 - - - 71106 RMVar_ID_71106 Human_SNP_ID_27251142 m1A Human chr1 - 109231003 109231003 109231003 TTCCCAGCTCTTACCTTCAAGAAGTACCCTCGACTCCCAGCCACCACGGCCCCCTTTTCGCCTTC TTCCCAGCTCTTACCTTCAAGAAGTACCCTCGGCTCCCAGCCACCACGGCCCCCTTTTCGCCTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109230952..109231049 26863196 MeRIP-seq:(Medium) rs1184068160 Functional Loss SNV dbSNP153 33..33 33 - - - 71107 RMVar_ID_71107 Human_SNP_ID_27252164 m1A Human chr1 + 109235325 109235325 109235325 TGCCCTGCACCGGGATGAGTGGCTCCGGCCGGAGGACCTGCCCATCAAGTATGCTGGCCTGTCTA TGCCCTGCACCGGGATGAGTGGCTCCGGCCGGCGGACCTGCCCATCAAGTATGCTGGCCTGTCTA A C SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:109231626..109236125 32194978 MeRIP-seq:(Medium) rs777225589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220994,Human_RBP_ID_320136,Human_RBP_ID_969660,Human_RBP_ID_1407601,Human_RBP_ID_9252955,Human_RBP_ID_10506661,Human_RBP_ID_18965761,Human_RBP_ID_22428487,Human_RBP_ID_23320922,Human_RBP_ID_26309786,Human_RBP_ID_27385375 RMVar_hsa_circ_33424,RMVar_hsa_circ_92435,RMVar_hsa_circ_135152 71108 RMVar_ID_71108 Human_SNP_ID_27252441 m1A Human chr1 + 109236544 109236529 109236544 AATCCGATATGGGCAAACCAAGAAGATGATGGACAAGGTAGATGGCCCCCAGGGAGGTGGGAAGC AATCCGATATGGGCAAAC_______________CAAGGTAGATGGCCCCCAGGGAGGTGGGAAGC CCAAGAAGATGATGGA C SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr1:109236493..109236583;chr1:109236466..109236567 26863196,32194978 MeRIP-seq:(Medium) rs1557720270 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_1407617,Human_RBP_ID_1721447,Human_RBP_ID_10506678,Human_RBP_ID_18546719 Human_Splice_Rec_105551,Human_Splice_Rec_105581 RMVar_hsa_circ_92435,RMVar_hsa_circ_135152 71109 RMVar_ID_71109 Human_SNP_ID_27252446 m1A Human chr1 + 109236544 109236544 109236544 AATCCGATATGGGCAAACCAAGAAGATGATGGACAAGGTAGATGGCCCCCAGGGAGGTGGGAAGC AATCCGATATGGGCAAACCAAGAAGATGATGGGCAAGGTAGATGGCCCCCAGGGAGGTGGGAAGC A G SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr1:109236493..109236583;chr1:109236466..109236567 26863196,32194978 MeRIP-seq:(Medium) rs200645763 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1407617,Human_RBP_ID_1721447,Human_RBP_ID_10506678,Human_RBP_ID_18546719 Human_Splice_Rec_105551,Human_Splice_Rec_105581 RMVar_hsa_circ_92435,RMVar_hsa_circ_135152 71110 RMVar_ID_71110 Human_SNP_ID_27252830 m1A Human chr1 - 109238000 109238000 109238000 GGTACATGGCACTGTTCCCCTCTCAGCTACGCAGTCAGATGGGGGCAGGGGGATGAATGGGTGCT GGTACATGGCACTGTTCCCCTCTCAGCTACGCGGTCAGATGGGGGCAGGGGGATGAATGGGTGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109237951..109238025 32194978 MeRIP-seq:(Medium) rs1209593719 Functional Loss SNV dbSNP153 33..33 33 - - - 71111 RMVar_ID_71111 Human_SNP_ID_27255907 m1A Human chr1 + 109249623 109249623 109249623 GGCCGCGGCGACAGGCAGCAGCCGCGGCGGGGACGCGGGGCGCGAGCGGGCGGCGCGGGACCGTC GGCCGCGGCGACAGGCAGCAGCCGCGGCGGGGGCGCGGGGCGCGAGCGGGCGGCGCGGGACCGTC A G CELSR2 Ensembl:ENSG00000143126 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:109249573..109250030 26863196 MeRIP-seq:(Medium) rs1011342287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4078183 71112 RMVar_ID_71112 Human_SNP_ID_27256042 m1A Human chr1 + 109250028 109250028 109250028 GCATGAGGCGCGGCGGGGCCGGCAGGAGCCGGAGGAGGAGCCGCCGCCGCCGTTGACCCGGCCGC GCATGAGGCGCGGCGGGGCCGGCAGGAGCCGGGGGAGGAGCCGCCGCCGCCGTTGACCCGGCCGC A G CELSR2 Ensembl:ENSG00000143126 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:109249928..109250082 26863410 MeRIP-seq:(Medium) rs902687573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072953 71113 RMVar_ID_71113 Human_SNP_ID_27257231 m1A Human chr1 + 109252969 109252969 109252969 ATGCCCAGATTATGTACCAGATTGTGGAGGGCAACATCCCTGAGGTCTTTCAGCTGGACATCTTC ATGCCCAGATTATGTACCAGATTGTGGAGGGCGACATCCCTGAGGTCTTTCAGCTGGACATCTTC A G CELSR2 Ensembl:ENSG00000143126 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109252918..109253168 32194978 MeRIP-seq:(Medium) rs1226734473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27385438 Human_miRNA_ID_1376402 71114 RMVar_ID_71114 Human_SNP_ID_27258804 m1A Human chr1 + 109258687 109258687 109258687 CCACATCCTCAACGTGAGCCTGTCGGTGGGCCAGCCGCCAGGGCCCGGGGGCGGGCCGCCCTTCC CCACATCCTCAACGTGAGCCTGTCGGTGGGCCGGCCGCCAGGGCCCGGGGGCGGGCCGCCCTTCC A G CELSR2 Ensembl:ENSG00000143126 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109258638..109258892 26863196 MeRIP-seq:(Medium) rs1340842116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3980411,Human_RBP_ID_8754057,Human_RBP_ID_18187178 71115 RMVar_ID_71115 Human_SNP_ID_27263704 m1A Human chr1 + 109272976 109272976 109272976 AGGCCGCCTTCCCTGGAGAGCAGGGCTGGGATAGCCTGCTGGGGCCTGGAGCAGAGAGACTGCCC AGGCCGCCTTCCCTGGAGAGCAGGGCTGGGATTGCCTGCTGGGGCCTGGAGCAGAGAGACTGCCC A T CELSR2 Ensembl:ENSG00000143126 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109272926..109272992 26863196 MeRIP-seq:(Medium) rs756520103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854974,Human_RBP_ID_3933749,Human_RBP_ID_3980547,Human_RBP_ID_5666319,Human_RBP_ID_8732245,Human_RBP_ID_18968606,Human_RBP_ID_23206014 Human_Splice_Rec_105651,Human_Splice_Rec_105671,Human_Splice_Rec_105683 RMVar_hsa_circ_28435,RMVar_hsa_circ_80736,RMVar_hsa_circ_91089,RMVar_hsa_circ_135158,RMVar_hsa_circ_135159,RMVar_hsa_circ_81130,RMVar_hsa_circ_135168 71116 RMVar_ID_71116 Human_SNP_ID_27264208 m1A Human chr1 + 109274094 109274094 109274094 GTTCCTACGCCCGAGGCTCCCTTCCCTTCCCCAGCCGCACTCATGCCCTGCTCCTGTCTTGTGCT GTTCCTACGCCCGAGGCTCCCTTCCCTTCCCCCGCCGCACTCATGCCCTGCTCCTGTCTTGTGCT A C CELSR2 Ensembl:ENSG00000143126 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109274044..109274157 26863196 MeRIP-seq:(Medium) rs1285914424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320172,Human_RBP_ID_17720377,Human_RBP_ID_18546758,Human_RBP_ID_18928508 Human_Splice_Rec_105656,Human_Splice_Rec_105676 Human_miRNA_ID_841367,Human_miRNA_ID_1355303,Human_miRNA_ID_2682764,Human_miRNA_ID_2694907 RMVar_hsa_circ_91089,RMVar_hsa_circ_135158 71117 RMVar_ID_71117 Human_SNP_ID_27264392 m1A Human chr1 + 109274650 109274650 109274650 GTGTGCCTCGTCCTGCCCGCACTGCCTCTCCCAGGAACTGGAAAAGCCCTGTCCGGTGAGGGGGC GTGTGCCTCGTCCTGCCCGCACTGCCTCTCCCGGGAACTGGAAAAGCCCTGTCCGGTGAGGGGGC A G CELSR2 Ensembl:ENSG00000143126 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109274599..109274850 32194978 MeRIP-seq:(Medium) rs972670882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3980592,Human_RBP_ID_27164449,Human_RBP_ID_27385474 Human_miRNA_ID_252933,Human_miRNA_ID_2038364,Human_miRNA_ID_2069195,Human_miRNA_ID_2802093,Human_miRNA_ID_3017344 RMVar_hsa_circ_91089,RMVar_hsa_circ_135158 71118 RMVar_ID_71118 Human_SNP_ID_27265759 m1A Human chr1 + 109279803 109279803 109279803 AGGCCGCTCACGTGGAAATGTCCAGTGAACCAATGCCAAGGAAGAAGATAAAATTCTCTGGGGCT AGGCCGCTCACGTGGAAATGTCCAGTGAACCACTGCCAAGGAAGAAGATAAAATTCTCTGGGGCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:109279752..109279851 32194978 MeRIP-seq:(Medium) rs1449135389 Functional Loss SNV dbSNP153 33..33 33 - - - 71119 RMVar_ID_71119 Human_SNP_ID_27295059 m1A Human chr1 + 109397761 109397761 109397761 CCGATGGGGCCAGACCAGCGCGGCAGCGGCGCAGCGGGCGGCGGCGGCGCGTCCAGCCGGTCCTG CCGATGGGGCCAGACCAGCGCGGCAGCGGCGCGGCGGGCGGCGGCGGCGCGTCCAGCCGGTCCTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:109397676..109397881;chr1:109397717..109397901 26863196 MeRIP-seq:(Medium) rs1306803412 Functional Loss SNV dbSNP153 33..33 33 - - - 71120 RMVar_ID_71120 Human_SNP_ID_27295078 m1A Human chr1 + 109397798 109397798 109397798 GCGGCGGCGGCGCGTCCAGCCGGTCCTGGCTGAGGGTCGACGGCGGCAGCAGCTGCAGGAGGAGG GCGGCGGCGGCGCGTCCAGCCGGTCCTGGCTGGGGGTCGACGGCGGCAGCAGCTGCAGGAGGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr1:109397602..109397907;chr1:109397598..109397847 26863196,26863410 MeRIP-seq:(Medium) rs1319068052 Functional Loss SNV dbSNP153 33..33 33 - - - 71121 RMVar_ID_71121 Human_SNP_ID_27295098 m1A Human chr1 - 109397846 109397846 109397846 GGGAGCTGCGGACGGCCTCTCGCGCTGGCCCCATGGCCTCGGCCTCCTCCTCCTCCTGCAGCTGC GGGAGCTGCGGACGGCCTCTCGCGCTGGCCCCGTGGCCTCGGCCTCCTCCTCCTCCTGCAGCTGC T C SORT1 Ensembl:ENSG00000134243 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:109397797..109397901 26863196 MeRIP-seq:(Medium) rs1212137615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746542,Human_RBP_ID_3980882,Human_RBP_ID_9319058,Human_RBP_ID_22428498 Human_miRNA_ID_845066 71122 RMVar_ID_71122 Human_SNP_ID_27298233 m1A Human chr1 - 109411065 109411065 109411065 TCTGGGACCTTTGTACAGTGTGATGCTCGAGCAATTGGCTCTGCTTCAGAGGGTGCCCAGAGCTC TCTGGGACCTTTGTACAGTGTGATGCTCGAGCGATTGGCTCTGCTTCAGAGGGTGCCCAGAGCTC T C PSMA5 Ensembl:ENSG00000143106 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109410002..109411971 32194978 MeRIP-seq:(Medium) rs143159595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320289,Human_RBP_ID_1407671,Human_RBP_ID_3936378,Human_RBP_ID_5666584,Human_RBP_ID_8280220,Human_RBP_ID_8953563,Human_RBP_ID_10507835,Human_RBP_ID_18965768,Human_RBP_ID_22427351,Human_RBP_ID_22870914,Human_RBP_ID_23321149,Human_RBP_ID_26767540 Human_Splice_Rec_105960,Human_Splice_Rec_105961,Human_Splice_Rec_105976,Human_Splice_Rec_105977,Human_Splice_Rec_105992,Human_Splice_Rec_105993 RMVar_hsa_circ_104745,RMVar_hsa_circ_135214,RMVar_hsa_circ_282746,RMVar_hsa_circ_348759,RMVar_hsa_circ_370671,RMVar_hsa_circ_301761,RMVar_hsa_circ_121549,RMVar_hsa_circ_135212,RMVar_hsa_circ_135213,RMVar_hsa_circ_135211,RMVar_hsa_circ_135215 71123 RMVar_ID_71123 Human_SNP_ID_27302089 m1A Human chr1 + 109426380 109426380 109426380 GCAGCGGCTACGCGGGGATTCTGAGGACCAACACGACTCCACCGGCACCCAACTCACCGGCAGCC GCAGCGGCTACGCGGGGATTCTGAGGACCAACGCGACTCCACCGGCACCCAACTCACCGGCAGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109426259..109426450 26863196 MeRIP-seq:(Medium) rs760604409 Functional Loss SNV dbSNP153 33..33 33 - - - 71124 RMVar_ID_71124 Human_SNP_ID_27311295 m1A Human chr1 + 109466658 109466658 109466658 CGGCGGCCGCAGCCTCTGAGAGCACGAACAGCAGCGCCCCCGCGTCCCAGCCAGCCAGCCAGCCA CGGCGGCCGCAGCCTCTGAGAGCACGAACAGCCGCGCCCCCGCGTCCCAGCCAGCCAGCCAGCCA A C SYPL2 Ensembl:ENSG00000143028 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109466608..109466858 26863196 MeRIP-seq:(Medium) rs1398754497 Functional Loss SNV dbSNP153 33..33 33 - - - 71125 RMVar_ID_71125 Human_SNP_ID_27315460 m1A Human chr1 + 109483983 109483983 109483983 GTGATGGCGGTGCGTGAACGCGCGGCGGCAGCAATGGCCGCTCTGGAGCGGCGGGTGCCGAGTCT GTGATGGCGGTGCGTGAACGCGCGGCGGCAGCCATGGCCGCTCTGGAGCGGCGGGTGCCGAGTCT A C ATXN7L2 Ensembl:ENSG00000162650 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109483910..109484031 26863196 MeRIP-seq:(Medium) rs1369518811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_106019,Human_Splice_Rec_106041 71126 RMVar_ID_71126 Human_SNP_ID_27315586 m1A Human chr1 + 109484200 109484200 109484200 ACTGGAGCCGCCGTCCGGCTCCCCGGCCCCCCAAACAAAGGACCCGCCGGGTCCTAGTGCCCGCC ACTGGAGCCGCCGTCCGGCTCCCCGGCCCCCCCAACAAAGGACCCGCCGGGTCCTAGTGCCCGCC A C ATXN7L2 Ensembl:ENSG00000162650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109484189..109484438 26863196 MeRIP-seq:(Medium) rs1557866182 Functional Loss SNV dbSNP153 33..33 33 - - - 71127 RMVar_ID_71127 Human_SNP_ID_27316023 m1A Human chr1 - 109486015 109486015 109486015 AAACACAGCTCAGAAGGGTCAGGGCCAGTTTTAGAGAGTCTCCAGCCTCTCCTTACCAGAGACTG AAACACAGCTCAGAAGGGTCAGGGCCAGTTTTGGAGAGTCTCCAGCCTCTCCTTACCAGAGACTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109486013..109486150 26863196 MeRIP-seq:(Medium) rs1300239576 Functional Loss SNV dbSNP153 33..33 33 - - - 71128 RMVar_ID_71128 Human_SNP_ID_27317424 m1A Human chr1 + 109491034 109491034 109491034 GCACCTGCCCCCGCCTTCCAGGTCCAACCCTGAGACCTGCCTGCCCAGCCTCCATGCCCCCCACC GCACCTGCCCCCGCCTTCCAGGTCCAACCCTGGGACCTGCCTGCCCAGCCTCCATGCCCCCCACC A G ATXN7L2 Ensembl:ENSG00000162650 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109490983..109491142 26863196 MeRIP-seq:(Medium) rs1451695250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109162 71129 RMVar_ID_71129 Human_SNP_ID_27318450 m1A Human chr1 - 109494366 109494366 109494366 GTCTCCCCTTTACTGCTGGGGTCCCTCCTCCAAGTCTCCCGGGGCTCCCAAGCGCTGCCCCTCCA GTCTCCCCTTTACTGCTGGGGTCCCTCCTCCAGGTCTCCCGGGGCTCCCAAGCGCTGCCCCTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109494316..109494404 26863196 MeRIP-seq:(Medium) rs1461400060 Functional Loss SNV dbSNP153 33..33 33 - - - 71130 RMVar_ID_71130 Human_SNP_ID_27322299 m1A Human chr1 - 109509597 109509588 109509597 CGGTCGGTGGGCTCCGGCGGGCTCAGCGGTCGAGGCGGTGGCAGGGTGAGCGGAGCGGGGCCCCG CGGTCGGTGGGCTCCGGCGGGCTCAGCGGTCG_________CAGGGTGAGCGGAGCGGGGCCCCG GCCACCGCCT G AMIGO1 Ensembl:ENSG00000181754 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109509548..109509675 26863196 MeRIP-seq:(Medium) rs1230945535 Functional Loss DEL dbSNP153 33..41 33 - - - 71131 RMVar_ID_71131 Human_SNP_ID_27331470 m1A Human chr1 + 109548668 109548668 109548668 GCAATAGACGGTGCCTCAGCCTGCCGAGCCGCAGTTTCCGTGGTGTGAGTGAGTCCGGGCCCGTG GCAATAGACGGTGCCTCAGCCTGCCGAGCCGCGGTTTCCGTGGTGTGAGTGAGTCCGGGCCCGTG A G GNAI3 Ensembl:ENSG00000065135 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109548601..109548850 26863196 MeRIP-seq:(Medium) rs1420784935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1407698,Human_RBP_ID_3980988,Human_RBP_ID_5311788,Human_RBP_ID_8755063,Human_RBP_ID_9270249,Human_RBP_ID_9356637,Human_RBP_ID_22025990,Human_RBP_ID_23321287,Human_RBP_ID_27164535 71132 RMVar_ID_71132 Human_SNP_ID_27337229 m1A Human chr1 - 109574039 109574039 109574039 AAGAGCAAGTGAAGAGGAAATGAGAAACACTTACTGCCCTGGCAGCTTCCCCAAAGTCAATCTTT AAGAGCAAGTGAAGAGGAAATGAGAAACACTTCCTGCCCTGGCAGCTTCCCCAAAGTCAATCTTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:109573876..109574050 32194978 MeRIP-seq:(Medium) rs774161191 Functional Loss SNV dbSNP153 33..33 33 - - - 71133 RMVar_ID_71133 Human_SNP_ID_27349101 m1A Human chr1 + 109625687 109625686 109625687 CCCCCAGGAGCTGTTCACCCGCTCACTGGCTGAGAGCGAGCTCCGTAGTGCCCCGTATGAGTTCC CCCCCAGGAGCTGTTCACCCGCTCACTGGCTG_GAGCGAGCTCCGTAGTGCCCCGTATGAGTTCC GA G AMPD2 Ensembl:ENSG00000116337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109625674..109625775 32194978 MeRIP-seq:(Medium) rs1237742891 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18968621,Human_RBP_ID_22536200,Human_RBP_ID_23321466 Human_Splice_Rec_106202,Human_Splice_Rec_106210,Human_Splice_Rec_106242,Human_Splice_Rec_106276,Human_Splice_Rec_106312,Human_Splice_Rec_106346,Human_Splice_Rec_106358,Human_Splice_Rec_106366,Human_Splice_Rec_106398,Human_Splice_Rec_106430,Human_Splice_Rec_106462,Human_Splice_Rec_106494,Human_Splice_Rec_106502,Human_Splice_Rec_106506,Human_Splice_Rec_106540,Human_Splice_Rec_106574,Human_Splice_Rec_106606,Human_Splice_Rec_106618,Human_Splice_Rec_106650 71134 RMVar_ID_71134 Human_SNP_ID_27349349 m1A Human chr1 + 109626401 109626401 109626401 GTGATGTGCTGGAACGGGAGTTTCAGCGGGTCACCATCTCTGGGGAGGAGAAGTGTGGGGTAAGT GTGATGTGCTGGAACGGGAGTTTCAGCGGGTCTCCATCTCTGGGGAGGAGAAGTGTGGGGTAAGT A T AMPD2 Ensembl:ENSG00000116337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109626350..109627017 32194978 MeRIP-seq:(Medium) rs773614792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18965777 Human_Splice_Rec_106214,Human_Splice_Rec_106215,Human_Splice_Rec_106246,Human_Splice_Rec_106247,Human_Splice_Rec_106280,Human_Splice_Rec_106281,Human_Splice_Rec_106316,Human_Splice_Rec_106317,Human_Splice_Rec_106350,Human_Splice_Rec_106351,Human_Splice_Rec_106362,Human_Splice_Rec_106370,Human_Splice_Rec_106371,Human_Splice_Rec_106402,Human_Splice_Rec_106403,Human_Splice_Rec_106434,Human_Splice_Rec_106435,Human_Splice_Rec_106466,Human_Splice_Rec_106467,Human_Splice_Rec_106510,Human_Splice_Rec_106511,Human_Splice_Rec_106544,Human_Splice_Rec_106545,Human_Splice_Rec_106578,Human_Splice_Rec_106579,Human_Splice_Rec_106610,Human_Splice_Rec_106611,Human_Splice_Rec_106622,Human_Splice_Rec_106623,Human_Splice_Rec_106654,Human_Splice_Rec_106658,Human_Splice_Rec_106659,Human_Splice_Rec_106685,Human_Splice_Rec_106688,Human_Splice_Rec_106689 71135 RMVar_ID_71135 Human_SNP_ID_27349619 m1A Human chr1 + 109627267 109627267 109627267 CCATGCCTGGGGACCTGGGCTTGGGTCTGCGCATGGTGCGGGGTGTGGTGCACGTCTACACCCGC CCATGCCTGGGGACCTGGGCTTGGGTCTGCGCGTGGTGCGGGGTGTGGTGCACGTCTACACCCGC A G AMPD2 Ensembl:ENSG00000116337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109627115..109627266 32194978 MeRIP-seq:(Medium) rs1246379614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8754067 Human_Splice_Rec_106218,Human_Splice_Rec_106219,Human_Splice_Rec_106250,Human_Splice_Rec_106251,Human_Splice_Rec_106284,Human_Splice_Rec_106285,Human_Splice_Rec_106320,Human_Splice_Rec_106321,Human_Splice_Rec_106374,Human_Splice_Rec_106375,Human_Splice_Rec_106406,Human_Splice_Rec_106407,Human_Splice_Rec_106438,Human_Splice_Rec_106439,Human_Splice_Rec_106470,Human_Splice_Rec_106471,Human_Splice_Rec_106514,Human_Splice_Rec_106515,Human_Splice_Rec_106548,Human_Splice_Rec_106549,Human_Splice_Rec_106582,Human_Splice_Rec_106583,Human_Splice_Rec_106614,Human_Splice_Rec_106626,Human_Splice_Rec_106627,Human_Splice_Rec_106662,Human_Splice_Rec_106663 71136 RMVar_ID_71136 Human_SNP_ID_27349933 m1A Human chr1 + 109628173 109628173 109628173 TCAAGCGGGCAATGAAGCGGCACCTGGAGGAGATCGTGCACGTGGAGCAGGGCCGTGAACAGACG TCAAGCGGGCAATGAAGCGGCACCTGGAGGAGCTCGTGCACGTGGAGCAGGGCCGTGAACAGACG A C AMPD2 Ensembl:ENSG00000116337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109628125..109628210 26863196 MeRIP-seq:(Medium) rs759460123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9359129,Human_RBP_ID_18968637,Human_RBP_ID_26314494 Human_Splice_Rec_106224,Human_Splice_Rec_106256,Human_Splice_Rec_106290,Human_Splice_Rec_106326,Human_Splice_Rec_106380,Human_Splice_Rec_106412,Human_Splice_Rec_106444,Human_Splice_Rec_106476,Human_Splice_Rec_106520,Human_Splice_Rec_106554,Human_Splice_Rec_106588,Human_Splice_Rec_106632,Human_Splice_Rec_106668,Human_Splice_Rec_106696,Human_Splice_Rec_106712 RMVar_hsa_circ_98274,RMVar_hsa_circ_376566,RMVar_hsa_circ_135227,RMVar_hsa_circ_135228 71137 RMVar_ID_71137 Human_SNP_ID_27357734 m1A Human chr1 - 109658911 109658911 109658911 AATCTCTAGTGTCCTCATCACATGCCCCCATTACCTTGTCTCCAACAAACCATGGCCTCTTCCCC AATCTCTAGTGTCCTCATCACATGCCCCCATTTCCTTGTCTCCAACAAACCATGGCCTCTTCCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:109658903..109658974 26863196 MeRIP-seq:(Medium) rs1389910415 Functional Loss SNV dbSNP153 33..33 33 - - - 71138 RMVar_ID_71138 Human_SNP_ID_27358433 m1A Human chr1 + 109661475 109661474 109661475 TTTGAAGCCTCAGCTACCCACTTTCCTTCATGAACATCCCCCTCCCAACACTACCCTTCCCTGCA TTTGAAGCCTCAGCTACCCACTTTCCTTCATG_ACATCCCCCTCCCAACACTACCCTTCCCTGCA GA G GSTM4 Ensembl:ENSG00000168765 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109661354..109661639 26863196 MeRIP-seq:(Medium) rs996754181 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17071541,Human_RBP_ID_17647599,Human_RBP_ID_18928516 RMVar_hsa_circ_135230 71139 RMVar_ID_71139 Human_SNP_ID_27418854 m1A Human chr1 + 109910573 109910573 109910573 TCCGCAGAGGGCGCGGGGAAGGCAGGGTGGGGACGCGGTGGAGCCCGCGCTCGTTTGCTGAAGGC TCCGCAGAGGGCGCGGGGAAGGCAGGGTGGGGTCGCGGTGGAGCCCGCGCTCGTTTGCTGAAGGC A T CSF1 Ensembl:ENSG00000184371 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:109910526..109910635;chr1:109910524..109910797 26863196 MeRIP-seq:(Medium) rs1261368938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23321508 Human_Splice_Rec_107413,Human_Splice_Rec_107421 71140 RMVar_ID_71140 Human_SNP_ID_27436345 m1A Human chr1 + 109984881 109984881 109984881 CGCCGTCGCTGTCCGGCTGCCTTGGGCTGCCGAACAGACAAGGCGTGGGCCACAGCACCTCAGAA CGCCGTCGCTGTCCGGCTGCCTTGGGCTGCCGGACAGACAAGGCGTGGGCCACAGCACCTCAGAA A G AHCYL1 Ensembl:ENSG00000168710 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109984830..109984930 32194978 MeRIP-seq:(Medium) rs955871577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3981161,Human_RBP_ID_5312628,Human_RBP_ID_5519890,Human_RBP_ID_8755066,Human_RBP_ID_8940000,Human_RBP_ID_9320094,Human_RBP_ID_22023611,Human_RBP_ID_22429519 RMVar_hsa_circ_135235,RMVar_hsa_circ_86921 71141 RMVar_ID_71141 Human_SNP_ID_27443166 m1A Human chr1 + 110016424 110016424 110016424 CGTCAATGATTCTGTTACCAAACAGAAGTTTGATAACTTGTACTGCTGCCGAGAATCCATTTTGG CGTCAATGATTCTGTTACCAAACAGAAGTTTGGTAACTTGTACTGCTGCCGAGAATCCATTTTGG A G AHCYL1 Ensembl:ENSG00000168710 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs567763788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23321562 Human_Splice_Rec_107520,Human_Splice_Rec_107521,Human_Splice_Rec_107552,Human_Splice_Rec_107553,Human_Splice_Rec_107596,Human_Splice_Rec_107597 RMVar_hsa_circ_20913,RMVar_hsa_circ_38762,RMVar_hsa_circ_301116,RMVar_hsa_circ_369446,RMVar_hsa_circ_135236 71142 RMVar_ID_71142 Human_SNP_ID_27447529 m1A Human chr1 + 110034718 110034718 110034718 CAGCCCCAGCCCCCGCCACCTCCGCCGCCGGCAGCCGCACAGCCACCACCCGGGGCACCGCGGGC CAGCCCCAGCCCCCGCCACCTCCGCCGCCGGCGGCCGCACAGCCACCACCCGGGGCACCGCGGGC A G STRIP1 Ensembl:ENSG00000143093 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:110034672..110034762;chr1:110034672..110034766 26863196 MeRIP-seq:(Medium) rs1264882071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224033,Human_RBP_ID_4074250,Human_RBP_ID_9356655,Human_RBP_ID_18415021,Human_RBP_ID_24360383,Human_RBP_ID_27798366 Human_Splice_Rec_107665,Human_Splice_Rec_107705,Human_Splice_Rec_107707 71143 RMVar_ID_71143 Human_SNP_ID_27449545 m1A Human chr1 - 110041782 110041782 110041782 GAGGGGCGTGACCACTGCAAAATTTGGTCACCATCCCAAACAGCATGATGGCAAATGGCTCATTG GAGGGGCGTGACCACTGCAAAATTTGGTCACCGTCCCAAACAGCATGATGGCAAATGGCTCATTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:110041643..110041843 32194978 MeRIP-seq:(Medium) rs755613448 Functional Loss SNV dbSNP153 33..33 33 - - - 71144 RMVar_ID_71144 Human_SNP_ID_27451556 m1A Human chr1 - 110049187 110049187 110049187 TTAAAGTGCTTGAGCAGCAGCAGCAGGACAGCAGAAATGGCCTTAACAATGACCTCTTTGTGGCG TTAAAGTGCTTGAGCAGCAGCAGCAGGACAGCCGAAATGGCCTTAACAATGACCTCTTTGTGGCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:110049136..110049236 32194978 MeRIP-seq:(Medium) rs777959189 Functional Loss SNV dbSNP153 33..33 33 - - - 71145 RMVar_ID_71145 Human_SNP_ID_27476367 m1A Human chr1 - 110150545 110150545 110150545 CCTGCGCCCTGGCAGCGCCGGCTCTGCGGAGCAGAACGGAGCTGGGCGGAGCGCTGCGCGCACTG CCTGCGCCCTGGCAGCGCCGGCTCTGCGGAGCTGAACGGAGCTGGGCGGAGCGCTGCGCGCACTG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:110150531..110150613 26863410 MeRIP-seq:(Medium) rs1196196200 Functional Loss SNV dbSNP153 33..33 33 - - - 71146 RMVar_ID_71146 Human_SNP_ID_27480343 m1A Human chr1 - 110167042 110167042 110167042 TCTGCTTGCCGCCTGCCTCACCAGCCACATTCAGTACACTCTGCTTATAGTCCACAGGCTCCTCG TCTGCTTGCCGCCTGCCTCACCAGCCACATTCTGTACACTCTGCTTATAGTCCACAGGCTCCTCG T A AL355990.1 Ensembl:ENSG00000227091 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:110166996..110167085 26863196 MeRIP-seq:(Medium) rs745555325 Functional Loss SNV dbSNP153 33..33 33 - - - 71147 RMVar_ID_71147 Human_SNP_ID_27488712 m1A Human chr1 - 110201657 110201657 110201657 TGACTCGGAGCGGGGGTTCTCCTGGCACTGGGAAAGCAGCAACCCCTGCACATGTATTGCTGGAG TGACTCGGAGCGGGGGTTCTCCTGGCACTGGGGAAGCAGCAACCCCTGCACATGTATTGCTGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110201612..110201718 32194978 MeRIP-seq:(Medium) rs965813745 Functional Loss SNV dbSNP153 33..33 33 - - - 71148 RMVar_ID_71148 Human_SNP_ID_27491158 m1A Human chr1 - 110211014 110211014 110211014 AGCCGGCTTCCCCGCAGCGGCGGCAGCGCAGCAGCAACAAGTCCTCCGAGCGGCTGCCGGGGCCA AGCCGGCTTCCCCGCAGCGGCGGCAGCGCAGCTGCAACAAGTCCTCCGAGCGGCTGCCGGGGCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:110210963..110211034 26863196 MeRIP-seq:(Medium) rs983010249 Functional Loss SNV dbSNP153 33..33 33 - - - 71149 RMVar_ID_71149 Human_SNP_ID_27494831 m1A Human chr1 + 110223855 110223855 110223855 CTTCCCCCCGGGACAGCACCTGCAGTGATACCAGCCCCCCTGCCCGGGAAGAGGGTATGATCGAG CTTCCCCCCGGGACAGCACCTGCAGTGATACCGGCCCCCCTGCCCGGGAAGAGGGTATGATCGAG A G KCNC4 Ensembl:ENSG00000116396 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:110223808..110223911 26863196 MeRIP-seq:(Medium) rs148139999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_107845,Human_Splice_Rec_107853,Human_Splice_Rec_107859,Human_Splice_Rec_107865,Human_Splice_Rec_107875 RMVar_hsa_circ_30372,RMVar_hsa_circ_271259,RMVar_hsa_circ_135248 71150 RMVar_ID_71150 Human_SNP_ID_27521459 m1A Human chr1 + 110339499 110339499 110339499 CGCTGTGTGAAACGAGCGCGGGGCGGCGGGTTACTCAGCTCCGCGGAGACGACCTCCGACGACCC CGCTGTGTGAAACGAGCGCGGGGCGGCGGGTTGCTCAGCTCCGCGGAGACGACCTCCGACGACCC A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:110339449..110339599 26863196 MeRIP-seq:(Medium) rs1557890295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224477,Human_RBP_ID_3981604 71151 RMVar_ID_71151 Human_SNP_ID_27521724 m1A Human chr1 - 110340004 110340004 110340004 CAGAACCCGACAGATGACTGATTTTCACACTTACATCACCGAAGCGTTTGAACTCATGAAACAGG CAGAACCCGACAGATGACTGATTTTCACACTTGCATCACCGAAGCGTTTGAACTCATGAAACAGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:110339903..110340052 26863196 MeRIP-seq:(Medium) rs1454026358 Functional Loss SNV dbSNP153 33..33 33 - - - 71152 RMVar_ID_71152 Human_SNP_ID_27521782 m1A Human chr1 - 110340152 110340152 110340152 GGGGAGCGGCTGCGGCGCCGGCTCACATACACAGCTTCTATCTTCAGAGGCCGGTCATAGAGCAC GGGGAGCGGCTGCGGCGCCGGCTCACATACACTGCTTCTATCTTCAGAGGCCGGTCATAGAGCAC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:110340050..110340175 26863410 MeRIP-seq:(Medium) rs559942192 Functional Loss SNV dbSNP153 33..33 33 - - - 71153 RMVar_ID_71153 Human_SNP_ID_27521816 m1A Human chr1 - 110340210 110340210 110340210 ACCACCTACAGAGGCCCCGACCACACTGGCTGATGGAGGATAAGTATCTTTGTCTAAAGGGGAGC ACCACCTACAGAGGCCCCGACCACACTGGCTGGTGGAGGATAAGTATCTTTGTCTAAAGGGGAGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:110339701..110340400 26863196 MeRIP-seq:(Medium) rs745709698 Functional Loss SNV dbSNP153 33..33 33 - - - 71154 RMVar_ID_71154 Human_SNP_ID_27521819 m1A Human chr1 + 110340216 110340216 110340216 CTTTAGACAAAGATACTTATCCTCCATCAGCCAGTGTGGTCGGGGCCTCTGTAGGTGGTCACCGG CTTTAGACAAAGATACTTATCCTCCATCAGCCGGTGTGGTCGGGGCCTCTGTAGGTGGTCACCGG A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:110340176..110340300 26863196 MeRIP-seq:(Medium) rs769664209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1407921,Human_RBP_ID_5519107,Human_RBP_ID_8280560,Human_RBP_ID_8732376,Human_RBP_ID_9252956,Human_RBP_ID_22014750,Human_RBP_ID_22124406,Human_RBP_ID_26837089,Human_RBP_ID_27164733 71155 RMVar_ID_71155 Human_SNP_ID_27522012 m1A Human chr1 - 110340839 110340839 110340839 CCTTTTCGGTAGTCTATGGTGCGTATGGTGCCAAATCGATCAAATTCTCGTGCCAGGGCAGCAAG CCTTTTCGGTAGTCTATGGTGCGTATGGTGCCGAATCGATCAAATTCTCGTGCCAGGGCAGCAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110340790..110340890 32194978 MeRIP-seq:(Medium) rs1557891349 Functional Loss SNV dbSNP153 33..33 33 - - - 71156 RMVar_ID_71156 Human_SNP_ID_27522158 m1A Human chr1 + 110341295 110341295 110341295 GGTTGGTCCTTGGACCGGGACAGAGGTGATCGAGATCTGCCCAGCAGCAGAGACCAGCCTAGGAA GGTTGGTCCTTGGACCGGGACAGAGGTGATCGGGATCTGCCCAGCAGCAGAGACCAGCCTAGGAA A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110341187..110341300 32194978 MeRIP-seq:(Medium) rs3738751 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5519112,Human_RBP_ID_10513096,Human_RBP_ID_18547123,Human_RBP_ID_22707131,Human_RBP_ID_26311609,Human_RBP_ID_27385687 GWAS_ID_8436,GWAS_ID_8437,GWAS_ID_8438 71157 RMVar_ID_71157 Human_SNP_ID_27537721 m1A Human chr1 - 110404001 110404001 110404001 GCGGGACCCTGTCAGATGAGCATGCTGGAGTGATATCTGTTCTAGCCCAGCAAGCAGCTAAGCTA GCGGGACCCTGTCAGATGAGCATGCTGGAGTGGTATCTGTTCTAGCCCAGCAAGCAGCTAAGCTA T C LAMTOR5 Ensembl:ENSG00000134248 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:110403951..110404050 32194978 MeRIP-seq:(Medium) rs770173012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320782,Human_RBP_ID_850240,Human_RBP_ID_4074252,Human_RBP_ID_8940001,Human_RBP_ID_17647029,Human_RBP_ID_22430747,Human_RBP_ID_22634104,Human_RBP_ID_26773132,Human_RBP_ID_26800771 Human_Splice_Rec_108318,Human_Splice_Rec_108319,Human_Splice_Rec_108324,Human_Splice_Rec_108325,Human_Splice_Rec_108328,Human_Splice_Rec_108329,Human_Splice_Rec_108334,Human_Splice_Rec_108335,Human_Splice_Rec_108340,Human_Splice_Rec_108341,Human_Splice_Rec_108344,Human_Splice_Rec_108345,Human_Splice_Rec_108350,Human_Splice_Rec_108351,Human_Splice_Rec_108356 Human_miRNA_ID_2068087 RMVar_hsa_circ_1768,RMVar_hsa_circ_110788,RMVar_hsa_circ_114631,RMVar_hsa_circ_135252,RMVar_hsa_circ_135251 71158 RMVar_ID_71158 Human_SNP_ID_27537728 m1A Human chr1 + 110404024 110404024 110404024 GAACAGATATCACTCCAGCATGCTCATCTGACAGGGTCCCGCGGCCTGGAAAATAGAGATGATAT GAACAGATATCACTCCAGCATGCTCATCTGACGGGGTCCCGCGGCCTGGAAAATAGAGATGATAT A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110403976..110404050 32194978 MeRIP-seq:(Medium) rs767308127 Functional Loss SNV dbSNP153 33..33 33 - - - 71159 RMVar_ID_71159 Human_SNP_ID_27537735 m1A Human chr1 - 110404038 110404038 110404038 CAATCAGGTGACATATATCATCTCTATTTTCCAGGCCGCGGGACCCTGTCAGATGAGCATGCTGG CAATCAGGTGACATATATCATCTCTATTTTCCGGGCCGCGGGACCCTGTCAGATGAGCATGCTGG T C LAMTOR5 Ensembl:ENSG00000134248 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr1:110404001..110404095;chr1:110403976..110404050;chr1:110403951..110404103 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1390255588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850240,Human_RBP_ID_4074252,Human_RBP_ID_8940001,Human_RBP_ID_22430748,Human_RBP_ID_22634104,Human_RBP_ID_26773132 RMVar_hsa_circ_1768,RMVar_hsa_circ_114631,RMVar_hsa_circ_135251 71160 RMVar_ID_71160 Human_SNP_ID_27538664 m1A Human chr1 + 110407491 110407491 110407491 CCGTGTCCCGGGGGTCGCGCGACGTCCCCGAGACGCCCTGGCCGGTACTCGCAGCTCGCGCCTTT CCGTGTCCCGGGGGTCGCGCGACGTCCCCGAGGCGCCCTGGCCGGTACTCGCAGCTCGCGCCTTT A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:110407489..110407675 26863196 MeRIP-seq:(Medium) rs1463526754 Functional Loss SNV dbSNP153 33..33 33 - - - 71161 RMVar_ID_71161 Human_SNP_ID_27538677 m1A Human chr1 - 110407532 110407532 110407532 GGCCTGTCCTGAGGTCGCGGCGGAGGAACTTGAGCGGAACGAAAGGCGCGAGCTGCGAGTACCGG GGCCTGTCCTGAGGTCGCGGCGGAGGAACTTGGGCGGAACGAAAGGCGCGAGCTGCGAGTACCGG T C LAMTOR5 Ensembl:ENSG00000134248 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:110407528..110407650 26863410 MeRIP-seq:(Medium) rs1273268965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22870918,Human_RBP_ID_27576070 RMVar_hsa_circ_114631,RMVar_hsa_circ_135251 71162 RMVar_ID_71162 Human_SNP_ID_27538717 m1A Human chr1 - 110407604 110407604 110407604 GTGGTCGGTGGGTGGGATGGAGGCGACCTTGGAGCAGCACTTGGAAGACACGTGAGTAGTGCGCG GTGGTCGGTGGGTGGGATGGAGGCGACCTTGGCGCAGCACTTGGAAGACACGTGAGTAGTGCGCG T G LAMTOR5 Ensembl:ENSG00000134248 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:110407576..110407675 26863196 MeRIP-seq:(Medium) rs1328169094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19989,Human_RBP_ID_320787,Human_RBP_ID_803563,Human_RBP_ID_860026,Human_RBP_ID_1721917,Human_RBP_ID_3981853,Human_RBP_ID_5109165,Human_RBP_ID_5136320,Human_RBP_ID_5311794,Human_RBP_ID_5412715,Human_RBP_ID_5455986,Human_RBP_ID_5668764,Human_RBP_ID_8280732,Human_RBP_ID_8940162,Human_RBP_ID_9320101,Human_RBP_ID_17647607,Human_RBP_ID_21879128,Human_RBP_ID_22427375,Human_RBP_ID_22778961,Human_RBP_ID_22870918,Human_RBP_ID_23206039,Human_RBP_ID_23322314 Human_Splice_Rec_108313,Human_Splice_Rec_108331,Human_Splice_Rec_108337,Human_Splice_Rec_108347,Human_Splice_Rec_108353 Human_miRNA_ID_2314186,Human_miRNA_ID_2317345,Human_miRNA_ID_2320501,Human_miRNA_ID_2323655,Human_miRNA_ID_2326830,Human_miRNA_ID_2518030,Human_miRNA_ID_2521208,Human_miRNA_ID_2773091,Human_miRNA_ID_2820404,Human_miRNA_ID_2826537,Human_miRNA_ID_2829687,Human_miRNA_ID_2833809,Human_miRNA_ID_2839174 RMVar_hsa_circ_114631,RMVar_hsa_circ_135251 71163 RMVar_ID_71163 Human_SNP_ID_27538731 m1A Human chr1 - 110407637 110407637 110407637 AGGACGTGCCGTGCCGCTGGGTTCTGAGCCGGAGTGGTCGGTGGGTGGGATGGAGGCGACCTTGG AGGACGTGCCGTGCCGCTGGGTTCTGAGCCGGGGTGGTCGGTGGGTGGGATGGAGGCGACCTTGG T C LAMTOR5 Ensembl:ENSG00000134248 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:110407493..110407707;chr1:110407470..110407650;chr1:110407452..110407761;chr1:110407444..110407743;chr1:110407498..110407725 26863196 MeRIP-seq:(Medium) rs147389383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320787,Human_RBP_ID_742813,Human_RBP_ID_803563,Human_RBP_ID_3981854,Human_RBP_ID_5109165,Human_RBP_ID_5136320,Human_RBP_ID_5311794,Human_RBP_ID_5412715,Human_RBP_ID_5455987,Human_RBP_ID_5483961,Human_RBP_ID_5668764,Human_RBP_ID_8940162,Human_RBP_ID_9320101,Human_RBP_ID_17674475,Human_RBP_ID_21879128,Human_RBP_ID_22427376,Human_RBP_ID_22531357,Human_RBP_ID_22870918,Human_RBP_ID_23206039,Human_RBP_ID_23322314 Human_Splice_Rec_108313,Human_Splice_Rec_108331,Human_Splice_Rec_108337,Human_Splice_Rec_108347,Human_Splice_Rec_108353 RMVar_hsa_circ_114631,RMVar_hsa_circ_135251 71164 RMVar_ID_71164 Human_SNP_ID_27708262 m1A Human chr1 + 111119931 111119931 111119931 AGTTTCTGTTCTAAATCAGTCCCAAAATTGCCACTGTGCAAAACTGATGAGCAAGTCAGCACTAT AGTTTCTGTTCTAAATCAGTCCCAAAATTGCCGCTGTGCAAAACTGATGAGCAAGTCAGCACTAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111119880..111120587 32194978 MeRIP-seq:(Medium) rs774735436 Functional Loss SNV dbSNP153 33..33 33 - - - 71165 RMVar_ID_71165 Human_SNP_ID_27713060 m1A Human chr1 + 111139688 111139686 111139688 CTCCGCTTTGCCTGGGACCAGGAAAAGACGCGAGAGACGGAACTCGGCATCAGGCACTGCTTGGG CTCCGCTTTGCCTGGGACCAGGAAAAGACGC__GAGACGGAACTCGGCATCAGGCACTGCTTGGG CGA C CEPT1 Ensembl:ENSG00000134255 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111139568..111139768 32194978 MeRIP-seq:(Medium) rs1217915098 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_108671,Human_Splice_Rec_108687,Human_Splice_Rec_108703 RMVar_hsa_circ_98018,RMVar_hsa_circ_103826,RMVar_hsa_circ_135271,RMVar_hsa_circ_88377,RMVar_hsa_circ_135272,RMVar_hsa_circ_135270 71166 RMVar_ID_71166 Human_SNP_ID_27713277 m1A Human chr1 + 111140305 111140305 111140305 GCGATATTTCTAGGGGTGTACTTGTTGGGGTCAGGGTAAGGCTGCGGAGCGCGGTCACCGGACGT GCGATATTTCTAGGGGTGTACTTGTTGGGGTCGGGGTAAGGCTGCGGAGCGCGGTCACCGGACGT A G CEPT1 Ensembl:ENSG00000134255 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:111140265..111140352 26863196 MeRIP-seq:(Medium) rs1256045154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_802191,Human_RBP_ID_856908,Human_RBP_ID_4074264,Human_RBP_ID_5456001,Human_RBP_ID_9342914,Human_RBP_ID_17180684,Human_RBP_ID_18415023,Human_RBP_ID_19035182 Human_Splice_Rec_108713 RMVar_hsa_circ_79567,RMVar_hsa_circ_98018,RMVar_hsa_circ_103826,RMVar_hsa_circ_135271,RMVar_hsa_circ_88377,RMVar_hsa_circ_135272,RMVar_hsa_circ_135270,RMVar_hsa_circ_135273 71167 RMVar_ID_71167 Human_SNP_ID_27787510 m1A Human chr1 + 111441266 111441265 111441266 TCAGTAACACTTGCAGGTCCAGGGGCTGGGAGAGGTTCTGTGGGCACAACGTGGTGGACGACCTG TCAGTAACACTTGCAGGTCCAGGGGCTGGGAG_GGTTCTGTGGGCACAACGTGGTGGACGACCTG GA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111441217..111441524 32194978 MeRIP-seq:(Medium) rs756857746 Functional Loss DEL dbSNP153 33..33 33 - - - 71168 RMVar_ID_71168 Human_SNP_ID_27787511 m1A Human chr1 + 111441266 111441266 111441266 TCAGTAACACTTGCAGGTCCAGGGGCTGGGAGAGGTTCTGTGGGCACAACGTGGTGGACGACCTG TCAGTAACACTTGCAGGTCCAGGGGCTGGGAGGGGTTCTGTGGGCACAACGTGGTGGACGACCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111441217..111441524 32194978 MeRIP-seq:(Medium) rs1421411647 Functional Loss SNV dbSNP153 33..33 33 - - - 71169 RMVar_ID_71169 Human_SNP_ID_27789535 m1A Human chr1 + 111449001 111449001 111449001 CGGGGATGGGCTGGGAGGGTCAGTCTCCGGGGAGGGGCGCCCTGGGCCGGGGTAAGGGAGCTCCC CGGGGATGGGCTGGGAGGGTCAGTCTCCGGGGCGGGGCGCCCTGGGCCGGGGTAAGGGAGCTCCC A C ATP5PB Ensembl:ENSG00000116459 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:111448998..111449228 26863410 MeRIP-seq:(Medium) rs1405197493 Functional Loss SNV dbSNP153 33..33 33 - - - 71170 RMVar_ID_71170 Human_SNP_ID_27789588 m1A Human chr1 + 111449113 111449113 111449113 TGCCGTTCCATGCAGGCGGGCGCATTTGGGGGAAGATTCCACTCCCGGGCCGCCGGGGGCACTAG TGCCGTTCCATGCAGGCGGGCGCATTTGGGGGGAGATTCCACTCCCGGGCCGCCGGGGGCACTAG A G ATP5PB Ensembl:ENSG00000116459 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111449062..111449179 32194978 MeRIP-seq:(Medium) rs992607622 Functional Loss SNV dbSNP153 33..33 33 - - - 71171 RMVar_ID_71171 Human_SNP_ID_27789643 m1A Human chr1 + 111449199 111449199 111449199 CATCTCCACGGTTCCAACTCCAACCTAGACTCAAACTGGACGCCGGCCGGAGACTCCGCTCCGGC CATCTCCACGGTTCCAACTCCAACCTAGACTCCAACTGGACGCCGGCCGGAGACTCCGCTCCGGC A C ATP5PB Ensembl:ENSG00000116459 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:111449076..111449233 26863196 MeRIP-seq:(Medium) rs1460081198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_109446 71172 RMVar_ID_71172 Human_SNP_ID_27789849 m1A Human chr1 - 111449513 111449501 111449514 GCATGGTCAACGAAAGTCCAGGTAGCAATCTTAGCGTCCCTGTGACCCCGATAGGAGAATCTGTC GCATGGTCAACGAAAGTCCAGGTAGCAATCT_____________ACCCCGATAGGAGAATCTGTC TCACAGGGACGCTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:111449451..111449612 26863196 MeRIP-seq:(Medium) rs753517331 Functional Loss DEL dbSNP153 32..44 33 - - - 71173 RMVar_ID_71173 Human_SNP_ID_27789868 m1A Human chr1 - 111449531 111449531 111449531 AAAGTACCACCCGGGACAGCATGGTCAACGAAAGTCCAGGTAGCAATCTTAGCGTCCCTGTGACC AAAGTACCACCCGGGACAGCATGGTCAACGAAGGTCCAGGTAGCAATCTTAGCGTCCCTGTGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:111449451..111449616 26863196 MeRIP-seq:(Medium) rs1351596855 Functional Loss SNV dbSNP153 33..33 33 - - - 71174 RMVar_ID_71174 Human_SNP_ID_27789870 m1A Human chr1 - 111449533 111449533 111449533 GGAAAGTACCACCCGGGACAGCATGGTCAACGAAAGTCCAGGTAGCAATCTTAGCGTCCCTGTGA GGAAAGTACCACCCGGGACAGCATGGTCAACGCAAGTCCAGGTAGCAATCTTAGCGTCCCTGTGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:111449501..111449575 26863196 MeRIP-seq:(Medium) rs200429045 Functional Loss SNV dbSNP153 33..33 33 - - - 71175 RMVar_ID_71175 Human_SNP_ID_27789986 m1A Human chr1 - 111449828 111449828 111449828 AGGCTGCATTCTTCAGAGAGGGGGCTGCAGATAGACAAGGCGAAGGTCAGCAAAGTCAAATGAAA AGGCTGCATTCTTCAGAGAGGGGGCTGCAGATTGACAAGGCGAAGGTCAGCAAAGTCAAATGAAA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111449826..111461082 32194978 MeRIP-seq:(Medium) rs748279498 Functional Loss SNV dbSNP153 33..33 33 - - - 71176 RMVar_ID_71176 Human_SNP_ID_27791051 m1A Human chr1 - 111454166 111454166 111454166 ATTGTACAAATGTAAAGCCTGTTTCTTTAAGGAGAATACAGTGTATGAATAATGAGCAGAAACAA ATTGTACAAATGTAAAGCCTGTTTCTTTAAGGCGAATACAGTGTATGAATAATGAGCAGAAACAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:111454164..111454250 26863196 MeRIP-seq:(Medium) rs1557799912 Functional Loss SNV dbSNP153 33..33 33 - - - 71177 RMVar_ID_71177 Human_SNP_ID_27830998 m1A Human chr1 - 111619936 111619936 111619936 TGGGGCCGTCTGGAGCTCCCCGCCCCTTACTCACCCCCCCGGTCCGGCGCCTCCTCCACCTCCTC TGGGGCCGTCTGGAGCTCCCCGCCCCTTACTCCCCCCCCCGGTCCGGCGCCTCCTCCACCTCCTC T G LOC107985184-001 RNACentral:URS0000E60A45 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:111619859..111619999;chr1:111619844..111620006 26863410 MeRIP-seq:(Medium) rs1030124422 Functional Loss SNV dbSNP153 33..33 33 - - - 71178 RMVar_ID_71178 Human_SNP_ID_27848888 m1A Human chr1 + 111691353 111691353 111691353 GTTTGTTTTTCAGATCGTCAGTATTTAAACAGATCACATCATGCGTGAGTACAAGCTAGTGGTCC GTTTGTTTTTCAGATCGTCAGTATTTAAACAGGTCACATCATGCGTGAGTACAAGCTAGTGGTCC A G RAP1A Ensembl:ENSG00000116473 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:111619794..111691425;chr1:111619790..111697441 26863196 MeRIP-seq:(Medium) rs144405448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_857036,Human_RBP_ID_4074276,Human_RBP_ID_8940003,Human_RBP_ID_26311615,Human_RBP_ID_27800622 Human_Splice_Rec_109576,Human_Splice_Rec_109577,Human_Splice_Rec_109592,Human_Splice_Rec_109593,Human_Splice_Rec_109602,Human_Splice_Rec_109603,Human_Splice_Rec_109616,Human_Splice_Rec_109617 RMVar_hsa_circ_119682,RMVar_hsa_circ_333183,RMVar_hsa_circ_135300,RMVar_hsa_circ_342534,RMVar_hsa_circ_334779,RMVar_hsa_circ_283654,RMVar_hsa_circ_135302,RMVar_hsa_circ_103032,RMVar_hsa_circ_135303,RMVar_hsa_circ_135301 71179 RMVar_ID_71179 Human_SNP_ID_27856682 m1A Human chr1 + 111725103 111725103 111725103 AGAGTGACCCTAACCACCGCGGCTGCGCCCCCATAATCCCATCTTGAGCTCTGCCCCTCTCTCCA AGAGTGACCCTAACCACCGCGGCTGCGCCCCCGTAATCCCATCTTGAGCTCTGCCCCTCTCTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:111724938..111725187 26863196 MeRIP-seq:(Medium) rs1178107471 Functional Loss SNV dbSNP153 33..33 33 - - - 71180 RMVar_ID_71180 Human_SNP_ID_27864638 m1A Human chr1 + 111755963 111755963 111755963 GCGGCATTTGAAGCCTCGGGAGCCTTAGCAGCAGTGGCGACTGCTATGCCGGCTGAGCATGTGGC GCGGCATTTGAAGCCTCGGGAGCCTTAGCAGCGGTGGCGACTGCTATGCCGGCTGAGCATGTGGC A G DDX20 Ensembl:ENSG00000064703 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:111755914..111756046 26863196 MeRIP-seq:(Medium) rs771815417 Functional Loss SNV dbSNP153 33..33 33 - - - 71181 RMVar_ID_71181 Human_SNP_ID_27918395 m1A Human chr1 - 111989758 111989752 111989758 GCGGCGGAGGCTGCGGCAGCGGCGGCGGCGGCAGTGGCGGCGGCAGTGGCGGCGGCAGTGGCGGC GCGGCGGAGGCTGCGGCAGCGGCGGCGGCGGC______GGCGGCAGTGGCGGCGGCAGTGGCGGC CGCCACT C lnc-KCND3-4 RNACentral:URS00008B53A3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:111989550..111989940 26863196 MeRIP-seq:(Medium) rs1260046166 Functional Loss DEL dbSNP153 33..38 33 - - - 71182 RMVar_ID_71182 Human_SNP_ID_27918399 m1A Human chr1 - 111989758 111989758 111989758 GCGGCGGAGGCTGCGGCAGCGGCGGCGGCGGCAGTGGCGGCGGCAGTGGCGGCGGCAGTGGCGGC GCGGCGGAGGCTGCGGCAGCGGCGGCGGCGGCGGTGGCGGCGGCAGTGGCGGCGGCAGTGGCGGC T C lnc-KCND3-4 RNACentral:URS00008B53A3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:111989550..111989940 26863196 MeRIP-seq:(Medium) rs1244977442 Functional Loss SNV dbSNP153 33..33 33 - - - 71183 RMVar_ID_71183 Human_SNP_ID_27918412 m1A Human chr1 - 111989773 111989773 111989773 CGAGCCGGGGCTGGAGCGGCGGAGGCTGCGGCAGCGGCGGCGGCGGCAGTGGCGGCGGCAGTGGC CGAGCCGGGGCTGGAGCGGCGGAGGCTGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGGCAGTGGC T C lnc-KCND3-4 RNACentral:URS00008B53A3 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:111989665..111989921 26863196 MeRIP-seq:(Medium) rs1427975823 Functional Loss SNV dbSNP153 33..33 33 - - - 71184 RMVar_ID_71184 Human_SNP_ID_28024227 m1A Human chr1 - 112396274 112396274 112396274 GCCATCACCAAGCCCCAGGGATAGTTGCTCCTACCTTTCCACGACGCTCCGGGCTCCGCTCCCCT GCCATCACCAAGCCCCAGGGATAGTTGCTCCTGCCTTTCCACGACGCTCCGGGCTCCGCTCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:112396259..112396360;chr1:112396256..112396339 26863196 MeRIP-seq:(Medium) rs1027393561 Functional Loss SNV dbSNP153 33..33 33 - - - 71185 RMVar_ID_71185 Human_SNP_ID_28038702 m1A Human chr1 - 112457204 112457204 112457204 TGGGTGGAGGGTTTCCTCTCTCAGCTCTGGGGATGGTTGGGGACTTGATTCCTGGAGACAGGGGG TGGGTGGAGGGTTTCCTCTCTCAGCTCTGGGGGTGGTTGGGGACTTGATTCCTGGAGACAGGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:112457154..112457266 26863196 MeRIP-seq:(Medium) rs759842819 Functional Loss SNV dbSNP153 33..33 33 - - - 71186 RMVar_ID_71186 Human_SNP_ID_28042370 m1A Human chr1 + 112473072 112473069 112473073 AGAGGGAGAGGAAAGAAAAAGGAAAGGAAGAAAAAGAAAGAAAGAAACACGGAAGGAGGAAGGAA AGAGGGAGAGGAAAGAAAAAGGAAAGGAAG____AGAAAGAAAGAAACACGGAAGGAGGAAGGAA GAAAA G WNT2B Ensembl:ENSG00000134245 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:112473025..112473155 26863196 MeRIP-seq:(Medium) rs1330621638 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_135315 71187 RMVar_ID_71187 Human_SNP_ID_28042384 m1A Human chr1 + 112473085 112473085 112473085 AGAAAAAGGAAAGGAAGAAAAAGAAAGAAAGAAACACGGAAGGAGGAAGGAAGGAAGGGAAAAAA AGAAAAAGGAAAGGAAGAAAAAGAAAGAAAGATACACGGAAGGAGGAAGGAAGGAAGGGAAAAAA A T WNT2B Ensembl:ENSG00000134245 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:112473034..112473144 26863196 MeRIP-seq:(Medium) rs1032066150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135315 71188 RMVar_ID_71188 Human_SNP_ID_28043225 m1A Human chr1 - 112476644 112476644 112476644 ATGCTGGGGTCCTCCTGCTCTACTTTTCTCCCACAGGTGGAGGTTGTGGGTTGTGTCCAGGAGAT ATGCTGGGGTCCTCCTGCTCTACTTTTCTCCCGCAGGTGGAGGTTGTGGGTTGTGTCCAGGAGAT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:112476626..112476711 26863410 MeRIP-seq:(Medium) rs968557414 Functional Loss SNV dbSNP153 33..33 33 - - - 71189 RMVar_ID_71189 Human_SNP_ID_28076700 m1A Human chr1 - 112619081 112619081 112619081 ATGGCGGACCGTGGCGGCGTGGGTGAAGCCGCAGCTGTTGGAGCGTCTCCTGCATCTGTCCCTGG ATGGCGGACCGTGGCGGCGTGGGTGAAGCCGCGGCTGTTGGAGCGTCTCCTGCATCTGTCCCTGG T C ST7L Ensembl:ENSG00000007341 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:112618794..112619125;chr1:112618788..112619125;chr1:112618853..112619125 26863196 MeRIP-seq:(Medium) rs774320953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8940163,Human_RBP_ID_22870921,Human_RBP_ID_23323478,Human_RBP_ID_26311618 Human_Splice_Rec_109938,Human_Splice_Rec_110244 RMVar_hsa_circ_77765,RMVar_hsa_circ_135353 71190 RMVar_ID_71190 Human_SNP_ID_28077040 m1A Human chr1 + 112619879 112619879 112619879 GGCCGACTTCGATGATCGTGTGTCGGATGAGGAGAAGGTAAGGGGTCCGCCTCTCTCTCTTACCT GGCCGACTTCGATGATCGTGTGTCGGATGAGGCGAAGGTAAGGGGTCCGCCTCTCTCTCTTACCT A C CAPZA1 Ensembl:ENSG00000116489 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:112619826..112619900 26863196 MeRIP-seq:(Medium) rs1396506066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_856728,Human_RBP_ID_1408431,Human_RBP_ID_4074277,Human_RBP_ID_5671623,Human_RBP_ID_10523548,Human_RBP_ID_22427386 Human_Splice_Rec_110253,Human_Splice_Rec_110257,Human_Splice_Rec_110271,Human_Splice_Rec_110287 RMVar_hsa_circ_101246,RMVar_hsa_circ_114420,RMVar_hsa_circ_135359,RMVar_hsa_circ_135360 71191 RMVar_ID_71191 Human_SNP_ID_28090148 m1A Human chr1 + 112674752 112674752 112674752 GAAAGCTCAGGTAAGAAAAGAACGGAGGAGGGAAGCCTGGTGGGGAGAAGGGAGCCCGCAGGATC GAAAGCTCAGGTAAGAAAAGAACGGAGGAGGGGAGCCTGGTGGGGAGAAGGGAGCCCGCAGGATC A G MOV10 Ensembl:ENSG00000155363 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:112674748..112674939 26863196 MeRIP-seq:(Medium) rs1361793856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9410641 71192 RMVar_ID_71192 Human_SNP_ID_28090179 m1A Human chr1 - 112674849 112674849 112674849 TCCGTGGAAATGAAACTGAAAGTCGCCGCTGCAGCTGGAAGTTGGCGGCCCTGAGATGAGGGTGC TCCGTGGAAATGAAACTGAAAGTCGCCGCTGCGGCTGGAAGTTGGCGGCCCTGAGATGAGGGTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:112674510..112675000;chr1:112674504..112675070 26863196 MeRIP-seq:(Medium) rs527969662 Functional Loss SNV dbSNP153 33..33 33 - - - 71193 RMVar_ID_71193 Human_SNP_ID_28097150 m1A Human chr1 + 112701425 112701425 112701425 CGGGGCTAGAAAACAATGCAGTCCTGGGCAGGAGGGAACTGAAAATGGGAGCCTTCAGCATGGAG CGGGGCTAGAAAACAATGCAGTCCTGGGCAGGGGGGAACTGAAAATGGGAGCCTTCAGCATGGAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr1:112701376..112701475;chr1:112701401..112701425 26863196 MeRIP-seq:(Medium) rs1361734281 Functional Loss SNV dbSNP153 33..33 33 - - - 71194 RMVar_ID_71194 Human_SNP_ID_28097654 m1A Human chr1 + 112703042 112703042 112703042 GGGCTGTCGATGGAGAAGCACATGAGGATGACATCAGTGTCCGGGTAGGAGAGAGGCCGCAGTCG GGGCTGTCGATGGAGAAGCACATGAGGATGACGTCAGTGTCCGGGTAGGAGAGAGGCCGCAGTCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:112703001..112703100 32194978 MeRIP-seq:(Medium) rs1009351299 Functional Loss SNV dbSNP153 33..33 33 - - - 71195 RMVar_ID_71195 Human_SNP_ID_28137814 m1A Human chr1 + 112850426 112850426 112850426 TGGGTATTAAAGACGAGTCGGGAAAGAAGAGCAGGTAAGAGGGCGGGGAGACTGGCCCAGTGGGT TGGGTATTAAAGACGAGTCGGGAAAGAAGAGCCGGTAAGAGGGCGGGGAGACTGGCCCAGTGGGT A C LINC01357 Ensembl:ENSG00000224167 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:112850396..112850495 32194978 MeRIP-seq:(Medium) rs1557824427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5540559 Human_Splice_Rec_110933,Human_Splice_Rec_110935,Human_Splice_Rec_110939 71196 RMVar_ID_71196 Human_SNP_ID_28155254 m1A Human chr1 - 112913776 112913776 112913776 GTGCTCAATGCAAATAGTAGACATTTGTGTGGAAATCATACCAGTTGTTCATTGATGGGATTTTT GTGCTCAATGCAAATAGTAGACATTTGTGTGGCAATCATACCAGTTGTTCATTGATGGGATTTTT T G SLC16A1 Ensembl:ENSG00000155380 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:112913726..112917291 32194978 MeRIP-seq:(Medium) rs1402452765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_321577,Human_RBP_ID_1408537,Human_RBP_ID_1722446,Human_RBP_ID_5672179,Human_RBP_ID_10525587,Human_RBP_ID_17180701,Human_RBP_ID_17444834,Human_RBP_ID_17674550,Human_RBP_ID_18214915,Human_RBP_ID_23205288,Human_RBP_ID_23323722,Human_RBP_ID_26389572,Human_RBP_ID_26798674,Human_RBP_ID_26837804,Human_RBP_ID_27165143,Human_RBP_ID_27385962 71197 RMVar_ID_71197 Human_SNP_ID_28155305 m1A Human chr1 + 112913964 112913964 112913964 CTTTCTGGTCCGGAGATTCTGCTGCTTTGGTAACTTCATTTGGCTTCCCAGCAACATCTATACTG CTTTCTGGTCCGGAGATTCTGCTGCTTTGGTAGCTTCATTTGGCTTCCCAGCAACATCTATACTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:112913915..112914072 26863196 MeRIP-seq:(Medium) rs886045067 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_294,Clinvar_Rec_2554 71198 RMVar_ID_71198 Human_SNP_ID_28159299 m1A Human chr1 - 112929352 112929352 112929352 TTGACATACTATTTTAATTTTATGTCTTTCAGATATTTGGATTTGACCTGCATTTTGGAATTTAT TTGACATACTATTTTAATTTTATGTCTTTCAGGTATTTGGATTTGACCTGCATTTTGGAATTTAT T C SLC16A1 Ensembl:ENSG00000155380 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:112929326..112929405;chr1:112929301..112929375 26863196 MeRIP-seq:(Medium) rs770356494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21998198 Human_Splice_Rec_110942,Human_Splice_Rec_110950,Human_Splice_Rec_110958,Human_Splice_Rec_110966,Human_Splice_Rec_110972,Human_Splice_Rec_110980 RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135401,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010,RMVar_hsa_circ_323574 71199 RMVar_ID_71199 Human_SNP_ID_28165871 m1A Human chr1 + 112956153 112956153 112956153 GTCCTTCGCTCGCTGCCTCGTTTGCTTGTTCCAGTACCCACGCAGCTAGCCAGTCACGTCGCAGC GTCCTTCGCTCGCTGCCTCGTTTGCTTGTTCCGGTACCCACGCAGCTAGCCAGTCACGTCGCAGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:112956052..112956169 26863196 MeRIP-seq:(Medium) rs886045088 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_295 71200 RMVar_ID_71200 Human_SNP_ID_28166202 m1A Human chr1 + 112956946 112956946 112956946 GGCGCCTGGTGGGTATTAAAGACGAGTCGGGAAAGAAGAGCAGGTAAGAGGGTGGGGAGACTGGC GGCGCCTGGTGGGTATTAAAGACGAGTCGGGACAGAAGAGCAGGTAAGAGGGTGGGGAGACTGGC A C SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:112956896..112957013 26863196 MeRIP-seq:(Medium) rs764796960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855050,Human_RBP_ID_5540716,Human_RBP_ID_5642712,Human_RBP_ID_9359188 Human_Splice_Rec_110981,Human_Splice_Rec_110993,Human_Splice_Rec_110997,Human_Splice_Rec_110999,Human_Splice_Rec_111003,Human_Splice_Rec_111009,Human_Splice_Rec_111019 71201 RMVar_ID_71201 Human_SNP_ID_28194843 m1A Human chr1 + 113073309 113073309 113073309 TAGATGGTACAGCCTTCAGCCGGGGCTTCGGGAGACAGTGCAGCCACCGAGCATCTCTGCTGAGC TAGATGGTACAGCCTTCAGCCGGGGCTTCGGGGGACAGTGCAGCCACCGAGCATCTCTGCTGAGC A G LRIG2 Ensembl:ENSG00000198799 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:113073247..113073347 26863196 MeRIP-seq:(Medium) rs1052607666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224761,Human_RBP_ID_4074289,Human_RBP_ID_21963130,Human_RBP_ID_22025227,Human_RBP_ID_26837922 71202 RMVar_ID_71202 Human_SNP_ID_28208713 m1A Human chr1 + 113126295 113126295 113126295 ATTATCATGAAATATTTGTGAAATTTCTCACCATGAATTTGGAGGGAACCTACTTTTATTTCTCG ATTATCATGAAATATTTGTGAAATTTCTCACCCTGAATTTGGAGGGAACCTACTTTTATTTCTCG A C LRIG2 Ensembl:ENSG00000198799 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10494151 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8439,GWAS_ID_8440,GWAS_ID_8441 71203 RMVar_ID_71203 Human_SNP_ID_28269842 m1A Human chr1 + 113390672 113390672 113390672 CTTCCCCCTTCACCTCCCCGCCCCCCCGCCTCAGCCTTTCCCGCCGCTCGGGCGCTGAGCCCAGG CTTCCCCCTTCACCTCCCCGCCCCCCCGCCTCCGCCTTTCCCGCCGCTCGGGCGCTGAGCCCAGG A C MAGI3 Ensembl:ENSG00000081026 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:113390608..113390759 26863196 MeRIP-seq:(Medium) rs1180606400 Functional Loss SNV dbSNP153 33..33 33 - - - 71204 RMVar_ID_71204 Human_SNP_ID_28269886 m1A Human chr1 - 113390844 113390844 113390844 CCGGCCGTTCCCAGACGCGAGACGCCCCTTGGACGCCCCTCCCGGCTGCGCTCCCCGGGGCTGAC CCGGCCGTTCCCAGACGCGAGACGCCCCTTGGGCGCCCCTCCCGGCTGCGCTCCCCGGGGCTGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:113390803..113390922 26863196 MeRIP-seq:(Medium) rs890679340 Functional Loss SNV dbSNP153 33..33 33 - - - 71205 RMVar_ID_71205 Human_SNP_ID_28329320 m1A Human chr1 + 113653873 113653873 113653873 GAGGACGACAGCTCTCAGGCCTTCATTTCAACACAGAATGGATCTCCCCGCCTGAACCGGGCAGA GAGGACGACAGCTCTCAGGCCTTCATTTCAACGCAGAATGGATCTCCCCGCCTGAACCGGGCAGA A G MAGI3 Ensembl:ENSG00000081026 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2359173 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17761 Human_Splice_Rec_111142,Human_Splice_Rec_111184,Human_Splice_Rec_111224,Human_Splice_Rec_111266 GWAS_ID_8442,GWAS_ID_8443,GWAS_ID_8444,GWAS_ID_8445,GWAS_ID_8446 RMVar_hsa_circ_4433,RMVar_hsa_circ_43524,RMVar_hsa_circ_65814,RMVar_hsa_circ_360372,RMVar_hsa_circ_55520,RMVar_hsa_circ_268019,RMVar_hsa_circ_69227,RMVar_hsa_circ_135455,RMVar_hsa_circ_59122,RMVar_hsa_circ_353328,RMVar_hsa_circ_373254,RMVar_hsa_circ_135456,RMVar_hsa_circ_316166,RMVar_hsa_circ_321292,RMVar_hsa_circ_135457,RMVar_hsa_circ_367407,RMVar_hsa_circ_61981,RMVar_hsa_circ_135460,RMVar_hsa_circ_29378,RMVar_hsa_circ_322177,RMVar_hsa_circ_287940,RMVar_hsa_circ_135462,RMVar_hsa_circ_135463,RMVar_hsa_circ_135461,RMVar_hsa_circ_357993,RMVar_hsa_circ_351711,RMVar_hsa_circ_135464,RMVar_hsa_circ_328130,RMVar_hsa_circ_284049 71206 RMVar_ID_71206 Human_SNP_ID_28353173 m1A Human chr1 - 113759320 113759320 113759320 TTTTGCTGTCGCCGTGGCGACTGGAGGCCTTCACTTTTAATCCCCCTCATTTTCCAGTTCATTCT TTTTGCTGTCGCCGTGGCGACTGGAGGCCTTCGCTTTTAATCCCCCTCATTTTCCAGTTCATTCT T C PHTF1 Ensembl:ENSG00000116793 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:113759276..113759450 26863196 MeRIP-seq:(Medium) rs1406223505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18450,Human_RBP_ID_860120,Human_RBP_ID_4072978,Human_RBP_ID_5412748,Human_RBP_ID_5432666,Human_RBP_ID_5456026,Human_RBP_ID_5484024,Human_RBP_ID_5673933,Human_RBP_ID_9319083,Human_RBP_ID_18428270,Human_RBP_ID_18548066,Human_RBP_ID_22023677,Human_RBP_ID_27386077 Human_miRNA_ID_2652821,Human_miRNA_ID_2754016 RMVar_hsa_circ_122548,RMVar_hsa_circ_135490 71207 RMVar_ID_71207 Human_SNP_ID_28353205 m1A Human chr1 + 113759435 113759432 113759435 AGCCCGGGAGCCCGGGAGGAGGAGGCGGCGGCAGCGGCGCTCGTCTTCTGCGGGCCGCGCCGGGA AGCCCGGGAGCCCGGGAGGAGGAGGCGGCG___GCGGCGCTCGTCTTCTGCGGGCCGCGCCGGGA GGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:113759276..113759492;chr1:113759162..113759464 26863196 MeRIP-seq:(Medium) rs1557987057 Functional Loss DEL dbSNP153 31..33 33 - - - 71208 RMVar_ID_71208 Human_SNP_ID_28365017 m1A Human chr1 + 113811993 113811993 113811993 AGCGAAGGTGGCGGCGGAGGCGGCAGGAGAAGAGGCTCAACAGGGCCTGGGACAGTTGGGGCTGC AGCGAAGGTGGCGGCGGAGGCGGCAGGAGAAGTGGCTCAACAGGGCCTGGGACAGTTGGGGCTGC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:113811813..113811999 26863196 MeRIP-seq:(Medium) rs763454304 Functional Loss SNV dbSNP153 33..33 33 - - - 71209 RMVar_ID_71209 Human_SNP_ID_28365120 m1A Human chr1 - 113812201 113812199 113812201 GGCGGTGGCGGCGCAGGAGGAGCCGGACAAAGAGGGGAAGGAGAAACCTCATGCTGGGGTCTCCC GGCGGTGGCGGCGCAGGAGGAGCCGGACAAAG__GGGAAGGAGAAACCTCATGCTGGGGTCTCCC CCT C RSBN1 Ensembl:ENSG00000081019 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:113812150..113812247 26863196 MeRIP-seq:(Medium) rs778904902 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3983688,Human_RBP_ID_18415606,Human_RBP_ID_26314529,Human_RBP_ID_27800628 RMVar_hsa_circ_135491,RMVar_hsa_circ_93511 71210 RMVar_ID_71210 Human_SNP_ID_28365138 m1A Human chr1 + 113812228 113812228 113812228 TCCCCTCTTTGTCCGGCTCCTCCTGCGCCGCCACCGCCCGTACTACGCGCACCGCTCCGACCTGC TCCCCTCTTTGTCCGGCTCCTCCTGCGCCGCCGCCGCCCGTACTACGCGCACCGCTCCGACCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:113811933..113812339;chr1:113811937..113812271 26863196 MeRIP-seq:(Medium) rs772730811 Functional Loss SNV dbSNP153 33..33 33 - - - 71211 RMVar_ID_71211 Human_SNP_ID_28387017 m1A Human chr1 - 113904698 113904698 113904698 GACTCTTAGGAAGATGCCGTACCTTGGCTCCGAGGACGTGGTGAAGGAGCTGAAGAAGGCTCTGT GACTCTTAGGAAGATGCCGTACCTTGGCTCCGTGGACGTGGTGAAGGAGCTGAAGAAGGCTCTGT T A AP4B1 Ensembl:ENSG00000134262 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:113904647..113904840 26863196 MeRIP-seq:(Medium) rs1271710076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22870925 Human_Splice_Rec_111903,Human_Splice_Rec_111921,Human_Splice_Rec_111934,Human_Splice_Rec_111935,Human_Splice_Rec_111964,Human_Splice_Rec_111965,Human_Splice_Rec_111980,Human_Splice_Rec_111981,Human_Splice_Rec_111987,Human_Splice_Rec_111994,Human_Splice_Rec_111995,Human_Splice_Rec_111997,Human_Splice_Rec_112006,Human_Splice_Rec_112007 RMVar_hsa_circ_135508,RMVar_hsa_circ_362551 71212 RMVar_ID_71212 Human_SNP_ID_28387023 m1A Human chr1 + 113904707 113904707 113904707 TCTTCAGCTCCTTCACCACGTCCTCGGAGCCAAGGTACGGCATCTTCCTAAGAGTCACAGGGCAG TCTTCAGCTCCTTCACCACGTCCTCGGAGCCATGGTACGGCATCTTCCTAAGAGTCACAGGGCAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:113904662..113904854 26863196 MeRIP-seq:(Medium) rs772403179 Functional Loss SNV dbSNP153 33..33 33 - - - 71213 RMVar_ID_71213 Human_SNP_ID_28387038 m1A Human chr1 + 113904738 113904738 113904738 AAGGTACGGCATCTTCCTAAGAGTCACAGGGCAGCTCCCACAGCTCCCACGGTAACTCGAGGGCT AAGGTACGGCATCTTCCTAAGAGTCACAGGGCTGCTCCCACAGCTCCCACGGTAACTCGAGGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:113904648..113904853 26863196 MeRIP-seq:(Medium) rs759557786 Functional Loss SNV dbSNP153 33..33 33 - - - 71214 RMVar_ID_71214 Human_SNP_ID_28393685 m1A Human chr1 + 113929673 113929673 113929673 CTGCGGAGCAAGGGGCCCGGCGGTAGCCCCGGACGGCAGCAGGAGGCCGAGGCGGGAGCGCGCGG CTGCGGAGCAAGGGGCCCGGCGGTAGCCCCGGTCGGCAGCAGGAGGCCGAGGCGGGAGCGCGCGG A T HIPK1 Ensembl:ENSG00000163349 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:113929626..113930533;chr1:113929625..113929977 26863196 MeRIP-seq:(Medium) rs958601685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3983811,Human_RBP_ID_9319084 RMVar_hsa_circ_81168,RMVar_hsa_circ_135511 71215 RMVar_ID_71215 Human_SNP_ID_28393724 m1A Human chr1 + 113929769 113929769 113929769 GGCTGGGTGGTGGAGCGGGAGGGAGGCTGAGGAGGCTCCCCCTGCGGGACGGGCGCGGGGACGGC GGCTGGGTGGTGGAGCGGGAGGGAGGCTGAGGTGGCTCCCCCTGCGGGACGGGCGCGGGGACGGC A T HIPK1 Ensembl:ENSG00000163349 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:113929626..113929990 26863196 MeRIP-seq:(Medium) rs1171296415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072979,Human_RBP_ID_5311800,Human_RBP_ID_9320112,Human_RBP_ID_9352378,Human_RBP_ID_9411234 RMVar_hsa_circ_81168,RMVar_hsa_circ_135511 71216 RMVar_ID_71216 Human_SNP_ID_28503928 m1A Human chr1 - 114368057 114368053 114368057 CAGAGAGGAGAGAAAGAGAGGGGAAGAGAGAGAGAGCGAAAAGAGAGAGAGAGGAAAGAGAGAGG CAGAGAGGAGAGAAAGAGAGGGGAAGAGAGAG____CGAAAAGAGAGAGAGAGGAAAGAGAGAGG GCTCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:114367983..114368113 26863196 MeRIP-seq:(Medium) rs370816716 Functional Loss DEL dbSNP153 33..36 33 - - - 71217 RMVar_ID_71217 Human_SNP_ID_28538832 m1A Human chr1 - 114510196 114510196 114510196 GAAACACGTTGTGAGGAAGCGTTTTGGCTGAAAGGGCCCGGGCCAGCGAGGTGTTGAGGGAGTAG GAAACACGTTGTGAGGAAGCGTTTTGGCTGAACGGGCCCGGGCCAGCGAGGTGTTGAGGGAGTAG T G TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:114510087..114510232 26863196 MeRIP-seq:(Medium) rs1476244991 Functional Loss SNV dbSNP153 33..33 33 - - - 71218 RMVar_ID_71218 Human_SNP_ID_28539094 m1A Human chr1 + 114510877 114510877 114510877 CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCACCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCCCCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:114510826..114511048 26863196 MeRIP-seq:(Medium) rs6691166 Functional Loss SNV dbSNP153 33..33 33 - - - 71219 RMVar_ID_71219 Human_SNP_ID_28539095 m1A Human chr1 + 114510877 114510877 114510877 CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCACCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCGCCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:114510826..114511048 26863196 MeRIP-seq:(Medium) rs6691166 Functional Loss SNV dbSNP153 33..33 33 - - - 71220 RMVar_ID_71220 Human_SNP_ID_28539209 m1A Human chr1 - 114511066 114511065 114511066 CGGCGGGTTCAAAGAGGAAAACATGGCGGAAAACAAAGGCGGCGGCGAGGCTGAGAGCGGCGGCG CGGCGGGTTCAAAGAGGAAAACATGGCGGAAA_CAAAGGCGGCGGCGAGGCTGAGAGCGGCGGCG GT G TRIM33 Ensembl:ENSG00000197323 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:114510599..114511183;chr1:114510598..114511186;chr1:114510620..114511175 26863196 MeRIP-seq:(Medium) rs1310371493 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5234486 71221 RMVar_ID_71221 Human_SNP_ID_28539911 m1A Human chr1 + 114513044 114513044 114513044 ATTGAAGAAGGCCCCTGTTGATCAGATGAAGGAACCTGTCTTGGAGAAGAGCAGGAGAGGAACAC ATTGAAGAAGGCCCCTGTTGATCAGATGAAGGGACCTGTCTTGGAGAAGAGCAGGAGAGGAACAC A G lnc-SYCP1-4,lnc-SYCP1-4:2,lnc-SYCP1-4:3,lnc-SYCP1-4:4 RNACentral:URS0000D56EE9,RNACentral:URS0000D592E8,RNACentral:URS0000D58524,RNACentral:URS0000D575BC lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:114513006..114513163 26863196 MeRIP-seq:(Medium) rs529925450 Functional Loss SNV dbSNP153 33..33 33 - - - 71222 RMVar_ID_71222 Human_SNP_ID_28556541 m1A Human chr1 + 114581525 114581525 114581525 ACTCACCGCTTCCCGCACACCAGGGGCTTCATAACCTTGATCAAAATACGGCAGCGCATCCACCA ACTCACCGCTTCCCGCACACCAGGGGCTTCATTACCTTGATCAAAATACGGCAGCGCATCCACCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:114576691..114581589 32194978 MeRIP-seq:(Medium) rs746558693 Functional Loss SNV dbSNP153 33..33 33 - - - 71223 RMVar_ID_71223 Human_SNP_ID_28556558 m1A Human chr1 - 114581582 114581571 114581583 CAGGCAAACCTGAGGTCCTCAGAATGGCGGGCACAGGTTTGGTGGCTGGAGAGGTTGTGGTGGAT CAGGCAAACCTGAGGTCCTCAGAATGGCGGG____________GGCTGGAGAGGTTGTGGTGGAT CACCAAACCTGTG C BCAS2 Ensembl:ENSG00000116752 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:114581332..114581625 26863196 MeRIP-seq:(Medium) rs1553231622 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_3984185 Human_Splice_Rec_112519,Human_Splice_Rec_112531 Human_miRNA_ID_2972142,Human_miRNA_ID_2972143,Human_miRNA_ID_3005324,Human_miRNA_ID_3005325 RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 71224 RMVar_ID_71224 Human_SNP_ID_28556569 m1A Human chr1 - 114581582 114581582 114581582 CAGGCAAACCTGAGGTCCTCAGAATGGCGGGCACAGGTTTGGTGGCTGGAGAGGTTGTGGTGGAT CAGGCAAACCTGAGGTCCTCAGAATGGCGGGCGCAGGTTTGGTGGCTGGAGAGGTTGTGGTGGAT T C BCAS2 Ensembl:ENSG00000116752 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:114581332..114581625 26863196 MeRIP-seq:(Medium) rs62621917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3984185 Human_Splice_Rec_112519,Human_Splice_Rec_112531 Human_miRNA_ID_2972142,Human_miRNA_ID_2972143,Human_miRNA_ID_3005324,Human_miRNA_ID_3005325 RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 71225 RMVar_ID_71225 Human_SNP_ID_28588999 m1A Human chr1 - 114716712 114716712 114716712 GGGCTGTTCATGGCGGTTCCGGGGTCTCCAACATTTTTCCCGGCTGTGGTCCTAAATCTGTCCAA GGGCTGTTCATGGCGGTTCCGGGGTCTCCAACGTTTTTCCCGGCTGTGGTCCTAAATCTGTCCAA T C NRAS Ensembl:ENSG00000213281 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114716651..114716750 26863196 MeRIP-seq:(Medium) rs1015402217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25928,Human_RBP_ID_322335,Human_RBP_ID_970207,Human_RBP_ID_1408959,Human_RBP_ID_3277767,Human_RBP_ID_4074300,Human_RBP_ID_5432680,Human_RBP_ID_5456041,Human_RBP_ID_5484048,Human_RBP_ID_5675867,Human_RBP_ID_8281883,Human_RBP_ID_8954369,Human_RBP_ID_10537182 Human_Splice_Rec_112821 71226 RMVar_ID_71226 Human_SNP_ID_28589655 m1A Human chr1 - 114718666 114718666 114718666 ATCGCTTGAAGAATATCACTCTGGATGATGCCAGTGCTCCTCGCCTAATGGTTCTTCGTCAGCCA ATCGCTTGAAGAATATCACTCTGGATGATGCCGGTGCTCCTCGCCTAATGGTTCTTCGTCAGCCA T C CSDE1 Ensembl:ENSG00000009307 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114718615..114718742 26863196 MeRIP-seq:(Medium) rs1483252623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322386,Human_RBP_ID_858278,Human_RBP_ID_1408989,Human_RBP_ID_1723004,Human_RBP_ID_3277789,Human_RBP_ID_5675954,Human_RBP_ID_8281913,Human_RBP_ID_8733139,Human_RBP_ID_8954389,Human_RBP_ID_10537279,Human_RBP_ID_17211514,Human_RBP_ID_17445108,Human_RBP_ID_17763965,Human_RBP_ID_18548312,Human_RBP_ID_22430794,Human_RBP_ID_23325237 Human_Splice_Rec_112864,Human_Splice_Rec_112865,Human_Splice_Rec_112902,Human_Splice_Rec_112903,Human_Splice_Rec_112938,Human_Splice_Rec_112939,Human_Splice_Rec_112974,Human_Splice_Rec_112975,Human_Splice_Rec_113006,Human_Splice_Rec_113007,Human_Splice_Rec_113038,Human_Splice_Rec_113039,Human_Splice_Rec_113074,Human_Splice_Rec_113075,Human_Splice_Rec_113077,Human_Splice_Rec_113110,Human_Splice_Rec_113111 Human_miRNA_ID_2088502,Human_miRNA_ID_2089383 RMVar_hsa_circ_114327,RMVar_hsa_circ_135556 71227 RMVar_ID_71227 Human_SNP_ID_28589878 m1A Human chr1 - 114719584 114719584 114719584 ACTGGCAAGTGCAGCGCCTGTAATGTTTGGCGAGTCTGGTGAGTTTTGTTGTTGTGGTTTGATTA ACTGGCAAGTGCAGCGCCTGTAATGTTTGGCGGGTCTGGTGAGTTTTGTTGTTGTGGTTTGATTA T C CSDE1 Ensembl:ENSG00000009307 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1247176941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10537327,Human_RBP_ID_17722284,Human_RBP_ID_18548318,Human_RBP_ID_18965857,Human_RBP_ID_21880443,Human_RBP_ID_22872372,Human_RBP_ID_23206055,Human_RBP_ID_23325241,Human_RBP_ID_26838344 Human_Splice_Rec_112863,Human_Splice_Rec_112901,Human_Splice_Rec_112937,Human_Splice_Rec_112973,Human_Splice_Rec_113005,Human_Splice_Rec_113037,Human_Splice_Rec_113073,Human_Splice_Rec_113109 RMVar_hsa_circ_1908,RMVar_hsa_circ_114327,RMVar_hsa_circ_307152,RMVar_hsa_circ_135556,RMVar_hsa_circ_316681,RMVar_hsa_circ_352189,RMVar_hsa_circ_340809,RMVar_hsa_circ_307470,RMVar_hsa_circ_276222,RMVar_hsa_circ_278572,RMVar_hsa_circ_19221,RMVar_hsa_circ_135558,RMVar_hsa_circ_135560,RMVar_hsa_circ_135561,RMVar_hsa_circ_135562,RMVar_hsa_circ_135559 71228 RMVar_ID_71228 Human_SNP_ID_28589913 m1A Human chr1 + 114719720 114719720 114719720 TCACATGGAAAAAGAGCTTCTTGCTATCTCCTACTTCATAGTTAATGAAGCCAAACTGAAAAAAA TCACATGGAAAAAGAGCTTCTTGCTATCTCCTGCTTCATAGTTAATGAAGCCAAACTGAAAAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:114719576..114719750 32194978 MeRIP-seq:(Medium) rs1474378767 Functional Loss SNV dbSNP153 33..33 33 - - - 71229 RMVar_ID_71229 Human_SNP_ID_28591233 m1A Human chr1 - 114725171 114725165 114725172 CTTATTCAGCCTGTGCTTTTAAGTGGGAGATAAAGGATGGAGTAGTAGAGGGAGATGAGGCCTAA CTTATTCAGCCTGTGCTTTTAAGTGGGAGAT_______GGAGTAGTAGAGGGAGATGAGGCCTAA CATCCTTT C CSDE1 Ensembl:ENSG00000009307 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114725169..114725250 26863196 MeRIP-seq:(Medium) rs760511100 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_5676032,Human_RBP_ID_9451583,Human_RBP_ID_22351905,Human_RBP_ID_23325265 RMVar_hsa_circ_1908,RMVar_hsa_circ_307152,RMVar_hsa_circ_352189,RMVar_hsa_circ_340809,RMVar_hsa_circ_307470,RMVar_hsa_circ_276222,RMVar_hsa_circ_19221,RMVar_hsa_circ_39269,RMVar_hsa_circ_18439,RMVar_hsa_circ_135558,RMVar_hsa_circ_135560,RMVar_hsa_circ_135559,RMVar_hsa_circ_58281,RMVar_hsa_circ_372518,RMVar_hsa_circ_57169,RMVar_hsa_circ_86260,RMVar_hsa_circ_135565,RMVar_hsa_circ_283408,RMVar_hsa_circ_357483,RMVar_hsa_circ_121887,RMVar_hsa_circ_66915,RMVar_hsa_circ_135567,RMVar_hsa_circ_135568,RMVar_hsa_circ_135566 71230 RMVar_ID_71230 Human_SNP_ID_28591235 m1A Human chr1 - 114725171 114725171 114725171 CTTATTCAGCCTGTGCTTTTAAGTGGGAGATAAAGGATGGAGTAGTAGAGGGAGATGAGGCCTAA CTTATTCAGCCTGTGCTTTTAAGTGGGAGATATAGGATGGAGTAGTAGAGGGAGATGAGGCCTAA T A CSDE1 Ensembl:ENSG00000009307 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114725169..114725250 26863196 MeRIP-seq:(Medium) rs776673279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5676032,Human_RBP_ID_9451583,Human_RBP_ID_22351905,Human_RBP_ID_23325265 RMVar_hsa_circ_1908,RMVar_hsa_circ_307152,RMVar_hsa_circ_352189,RMVar_hsa_circ_340809,RMVar_hsa_circ_307470,RMVar_hsa_circ_276222,RMVar_hsa_circ_19221,RMVar_hsa_circ_39269,RMVar_hsa_circ_18439,RMVar_hsa_circ_135558,RMVar_hsa_circ_135560,RMVar_hsa_circ_135559,RMVar_hsa_circ_58281,RMVar_hsa_circ_372518,RMVar_hsa_circ_57169,RMVar_hsa_circ_86260,RMVar_hsa_circ_135565,RMVar_hsa_circ_283408,RMVar_hsa_circ_357483,RMVar_hsa_circ_121887,RMVar_hsa_circ_66915,RMVar_hsa_circ_135567,RMVar_hsa_circ_135568,RMVar_hsa_circ_135566 71231 RMVar_ID_71231 Human_SNP_ID_28594502 m1A Human chr1 + 114738020 114738020 114738020 AGGATTTCTTGTTTTATCTTCACCAGTTTAACAGCAATGGGTTTCCCAGTCCGTCGGTCCGATGA AGGATTTCTTGTTTTATCTTCACCAGTTTAACGGCAATGGGTTTCCCAGTCCGTCGGTCCGATGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114737931..114738044 26863196 MeRIP-seq:(Medium) rs1241777908 Functional Loss SNV dbSNP153 33..33 33 - - - 71232 RMVar_ID_71232 Human_SNP_ID_28599350 m1A Human chr1 - 114757848 114757848 114757848 GGGAAGGGCTGAGAATAAGACCAAGGCTAACGAGAAGCCTTCTGAGTCAAGGTGGGCACTCGTAG GGGAAGGGCTGAGAATAAGACCAAGGCTAACGCGAAGCCTTCTGAGTCAAGGTGGGCACTCGTAG T G CSDE1 Ensembl:ENSG00000009307 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:114757846..114757975 26863196 MeRIP-seq:(Medium) rs867753378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10539023 RMVar_hsa_circ_86260,RMVar_hsa_circ_135568 71233 RMVar_ID_71233 Human_SNP_ID_28604550 m1A Human chr1 + 114780501 114780501 114780501 CCGCCTCCCGCATAGCTGCTACCCGCCGGTGCAGCGCCGCCGACTGATCCACCAGCGACTCGGCG CCGCCTCCCGCATAGCTGCTACCCGCCGGTGCTGCGCCGCCGACTGATCCACCAGCGACTCGGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr1:114780451..114780675;chr1:114780426..114780585 26863196,32194978 MeRIP-seq:(Medium) rs756421782 Functional Loss SNV dbSNP153 33..33 33 - - - 71234 RMVar_ID_71234 Human_SNP_ID_28604606 m1A Human chr1 + 114780608 114780608 114780608 TCTGTCAGGATCTTCTCGATGGTGCAGCTCATAGCAGCAGCACCACCCCAGCCCCTGCCGGGCTC TCTGTCAGGATCTTCTCGATGGTGCAGCTCATTGCAGCAGCACCACCCCAGCCCCTGCCGGGCTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:114780387..114780634 26863196 MeRIP-seq:(Medium) rs758357526 Functional Loss SNV dbSNP153 33..33 33 - - - 71235 RMVar_ID_71235 Human_SNP_ID_28814385 m1A Human chr1 + 115642019 115642019 115642019 GGCGGGGCTCTGCCTCTCCAGGAGCCCAGCGCAGGCCGCAGAGCCGGGGCCGCTGTGAGCCGAGA GGCGGGGCTCTGCCTCTCCAGGAGCCCAGCGCTGGCCGCAGAGCCGGGGCCGCTGTGAGCCGAGA A T VANGL1 Ensembl:ENSG00000173218 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:115641973..115642155;chr1:115641970..115642210 26863196 MeRIP-seq:(Medium) rs1470571580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072981 Human_Splice_Rec_113609,Human_Splice_Rec_113623 Human_miRNA_ID_2394194,Human_miRNA_ID_3067757 RMVar_hsa_circ_85925,RMVar_hsa_circ_135585 71236 RMVar_ID_71236 Human_SNP_ID_28814389 m1A Human chr1 + 115642028 115642028 115642028 CTGCCTCTCCAGGAGCCCAGCGCAGGCCGCAGAGCCGGGGCCGCTGTGAGCCGAGACCGCGGGCC CTGCCTCTCCAGGAGCCCAGCGCAGGCCGCAGGGCCGGGGCCGCTGTGAGCCGAGACCGCGGGCC A G VANGL1 Ensembl:ENSG00000173218 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:115641977..115642193 26863196 MeRIP-seq:(Medium) rs1054421809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072981 Human_Splice_Rec_113609,Human_Splice_Rec_113623 Human_miRNA_ID_2394194,Human_miRNA_ID_3067757 RMVar_hsa_circ_85925,RMVar_hsa_circ_135585 71237 RMVar_ID_71237 Human_SNP_ID_28815721 m1A Human chr1 + 115647908 115647908 115647908 GTAGGAAATGTGCACTTGGGATTTAGTCTTTCAGTAAGTATTTGTTGGGTACCTGCTATGTTCAA GTAGGAAATGTGCACTTGGGATTTAGTCTTTCGGTAAGTATTTGTTGGGTACCTGCTATGTTCAA A G VANGL1 Ensembl:ENSG00000173218 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:115647906..115648124 26863196 MeRIP-seq:(Medium) rs1391717398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85925,RMVar_hsa_circ_135585 71238 RMVar_ID_71238 Human_SNP_ID_28897409 m1A Human chr1 - 115976383 115976383 115976383 GAGCGGGGAGCGCAGCCGGGCTACGCGGGGCGAGGGGCGAGGAGGGCGTTCGAGATCCGGGGCTG GAGCGGGGAGCGCAGCCGGGCTACGCGGGGCGGGGGGCGAGGAGGGCGTTCGAGATCCGGGGCTG T C LOC101928977,LOC101928977:2,LOC101928977:3 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:115976333..115976398 26863196 MeRIP-seq:(Medium) rs1241812437 Functional Loss SNV dbSNP153 33..33 33 - - - 71239 RMVar_ID_71239 Human_SNP_ID_28897515 m1A Human chr1 - 115976596 115976596 115976596 TGGCGGGCCGCGCGCAGGAACCCCGCCACCCCACCGCCCTCTCAGGCGCTGCCCTCCCGCCCAGC TGGCGGGCCGCGCGCAGGAACCCCGCCACCCCGCCGCCCTCTCAGGCGCTGCCCTCCCGCCCAGC T C LOC101928977,LOC101928977:2,LOC101928977:3,LOC101928977:4 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731,RNACentral:URS0000D5DBEE lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:115976549..115976668 26863196 MeRIP-seq:(Medium) rs779391414 Functional Loss SNV dbSNP153 33..33 33 - - - 71240 RMVar_ID_71240 Human_SNP_ID_28897523 m1A Human chr1 - 115976609 115976609 115976609 TCCTCCACCTCCATGGCGGGCCGCGCGCAGGAACCCCGCCACCCCACCGCCCTCTCAGGCGCTGC TCCTCCACCTCCATGGCGGGCCGCGCGCAGGAGCCCCGCCACCCCACCGCCCTCTCAGGCGCTGC T C LOC101928977,LOC101928977:2,LOC101928977:3,LOC101928977:4 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731,RNACentral:URS0000D5DBEE lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:115976558..115976709 26863196 MeRIP-seq:(Medium) rs1366197876 Functional Loss SNV dbSNP153 33..33 33 - - - 71241 RMVar_ID_71241 Human_SNP_ID_28897525 m1A Human chr1 - 115976613 115976613 115976613 CGCCTCCTCCACCTCCATGGCGGGCCGCGCGCAGGAACCCCGCCACCCCACCGCCCTCTCAGGCG CGCCTCCTCCACCTCCATGGCGGGCCGCGCGCGGGAACCCCGCCACCCCACCGCCCTCTCAGGCG T C LOC101928977,LOC101928977:2,LOC101928977:3,LOC101928977:4 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731,RNACentral:URS0000D5DBEE lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:115976564..115976666 26863196 MeRIP-seq:(Medium) rs1163423111 Functional Loss SNV dbSNP153 33..33 33 - - - 71242 RMVar_ID_71242 Human_SNP_ID_28940508 m1A Human chr1 + 116160356 116160356 116160356 TCTCAAAGTCTCAGTTGTTTTTTTTTTTTTTTAAATCTGGAAAACAGAAATAATAATATCTACCT TCTCAAAGTCTCAGTTGTTTTTTTTTTTTTTTTAATCTGGAAAACAGAAATAATAATATCTACCT A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:116160336..116160425 26863410 MeRIP-seq:(Medium) rs1194440955 Functional Loss SNV dbSNP153 33..33 33 - - - 71243 RMVar_ID_71243 Human_SNP_ID_28993583 m1A Human chr1 + 116373274 116373249 116373274 CTGGAGCTGCGGCGGGGTCTGGGGCGCAGAGCAGCGGCGGGAGGAGGCGGACACGTGGCAACAGC CTGGAGCT_________________________GCGGCGGGAGGAGGCGGACACGTGGCAACAGC TGCGGCGGGGTCTGGGGCGCAGAGCA T ATP1A1 Ensembl:ENSG00000163399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116373226..116373400 26863196 MeRIP-seq:(Medium) rs913452301 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_1428,Human_RBP_ID_224506,Human_RBP_ID_745498,Human_RBP_ID_4072982,Human_RBP_ID_5311802,Human_RBP_ID_5519135,Human_RBP_ID_8940165,Human_RBP_ID_9319088,Human_RBP_ID_22428522,Human_RBP_ID_24358466,Human_RBP_ID_26838523 71244 RMVar_ID_71244 Human_SNP_ID_28993603 m1A Human chr1 + 116373269 116373269 116373269 GCGGGCTGGAGCTGCGGCGGGGTCTGGGGCGCAGAGCAGCGGCGGGAGGAGGCGGACACGTGGCA GCGGGCTGGAGCTGCGGCGGGGTCTGGGGCGCGGAGCAGCGGCGGGAGGAGGCGGACACGTGGCA A G ATP1A1 Ensembl:ENSG00000163399 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116373214..116373355 26863196 MeRIP-seq:(Medium) rs1338433279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1428,Human_RBP_ID_224506,Human_RBP_ID_745498,Human_RBP_ID_4072982,Human_RBP_ID_5311802,Human_RBP_ID_5519135,Human_RBP_ID_8940165,Human_RBP_ID_9319088,Human_RBP_ID_22428522,Human_RBP_ID_24358466,Human_RBP_ID_26838523 71245 RMVar_ID_71245 Human_SNP_ID_28993606 m1A Human chr1 + 116373274 116373274 116373274 CTGGAGCTGCGGCGGGGTCTGGGGCGCAGAGCAGCGGCGGGAGGAGGCGGACACGTGGCAACAGC CTGGAGCTGCGGCGGGGTCTGGGGCGCAGAGCGGCGGCGGGAGGAGGCGGACACGTGGCAACAGC A G ATP1A1 Ensembl:ENSG00000163399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116373226..116373400 26863196 MeRIP-seq:(Medium) rs1352976570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1428,Human_RBP_ID_224506,Human_RBP_ID_745498,Human_RBP_ID_4072982,Human_RBP_ID_5311802,Human_RBP_ID_5519135,Human_RBP_ID_8940165,Human_RBP_ID_9319088,Human_RBP_ID_22428522,Human_RBP_ID_24358466,Human_RBP_ID_26838523 71246 RMVar_ID_71246 Human_SNP_ID_28993662 m1A Human chr1 - 116373370 116373370 116373370 GAGCTAGGGCTGCCGCGGGGCGGGAGGGTGGGAGGGCGGCCGGCGGCTCGGGCCGATGCCGCCGC GAGCTAGGGCTGCCGCGGGGCGGGAGGGTGGGGGGGCGGCCGGCGGCTCGGGCCGATGCCGCCGC T C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:116373303..116373454 26863410 MeRIP-seq:(Medium) rs1007805597 Functional Loss SNV dbSNP153 33..33 33 - - - 71247 RMVar_ID_71247 Human_SNP_ID_28993732 m1A Human chr1 + 116373479 116373479 116373479 CTCTGTGCTTTTCTCTCTGATTCTCCAGCGACAGGACCCGGCGCCGGGCACTGAGCACCGCCACC CTCTGTGCTTTTCTCTCTGATTCTCCAGCGACCGGACCCGGCGCCGGGCACTGAGCACCGCCACC A C ATP1A1 Ensembl:ENSG00000163399 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:116373201..116373629;chr1:116373430..116373632 26863196 MeRIP-seq:(Medium) rs1557775838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25571,Human_RBP_ID_224507,Human_RBP_ID_322766,Human_RBP_ID_970303,Human_RBP_ID_1409200,Human_RBP_ID_3277977,Human_RBP_ID_3984884,Human_RBP_ID_5432705,Human_RBP_ID_5456057,Human_RBP_ID_5676930,Human_RBP_ID_8240072,Human_RBP_ID_8733290,Human_RBP_ID_8954517,Human_RBP_ID_9319090,Human_RBP_ID_17211601,Human_RBP_ID_17722527,Human_RBP_ID_18187217,Human_RBP_ID_22428525,Human_RBP_ID_22485585,Human_RBP_ID_22532138,Human_RBP_ID_23325778,Human_RBP_ID_27386364 Human_Splice_Rec_113811,Human_Splice_Rec_113855 71248 RMVar_ID_71248 Human_SNP_ID_28997218 m1A Human chr1 - 116387449 116387449 116387449 TGAGGTTCCTCTTCTGTAGCAGCTTGGATGCTATAAGCCAAGAAACAAAGAATCGCTCCAATCCA TGAGGTTCCTCTTCTGTAGCAGCTTGGATGCTGTAAGCCAAGAAACAAAGAATCGCTCCAATCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:116387276..116388277 32194978 MeRIP-seq:(Medium) rs1203550548 Functional Loss SNV dbSNP153 33..33 33 - - - 71249 RMVar_ID_71249 Human_SNP_ID_28997905 m1A Human chr1 - 116390288 116390288 116390288 TTTATCAGAGCAGATGGTGGACGTGGACCCCAAGGTCTCCACAGCTTCTAAGTTCTTCACTAAGC TTTATCAGAGCAGATGGTGGACGTGGACCCCAGGGTCTCCACAGCTTCTAAGTTCTTCACTAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:116390237..116390357 26863196 MeRIP-seq:(Medium) rs1425795255 Functional Loss SNV dbSNP153 33..33 33 - - - 71250 RMVar_ID_71250 Human_SNP_ID_28998560 m1A Human chr1 + 116392883 116392883 116392883 CAGCGGGCAGTTGCAGGAGATGCCTCTGAGTCAGCACTCTTAAAGTGCATAGAGCTGTGCTGTGG CAGCGGGCAGTTGCAGGAGATGCCTCTGAGTCGGCACTCTTAAAGTGCATAGAGCTGTGCTGTGG A G ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:116390401..116392884 32194978 MeRIP-seq:(Medium) rs755045434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322792,Human_RBP_ID_744035,Human_RBP_ID_802573,Human_RBP_ID_857869,Human_RBP_ID_970312,Human_RBP_ID_1409247,Human_RBP_ID_1723216,Human_RBP_ID_3278008,Human_RBP_ID_5677021,Human_RBP_ID_8282161,Human_RBP_ID_8954534,Human_RBP_ID_9266124,Human_RBP_ID_17338348,Human_RBP_ID_17456526,Human_RBP_ID_17722555,Human_RBP_ID_18187227,Human_RBP_ID_18548546,Human_RBP_ID_19151226,Human_RBP_ID_22430809,Human_RBP_ID_22749377,Human_RBP_ID_22779267,Human_RBP_ID_22872400,Human_RBP_ID_23325829,Human_RBP_ID_26838566,Human_RBP_ID_27165702 Human_Splice_Rec_113830,Human_Splice_Rec_113878,Human_Splice_Rec_113932 Human_miRNA_ID_2453175,Human_miRNA_ID_2773103,Human_miRNA_ID_2948237 RMVar_hsa_circ_12349,RMVar_hsa_circ_358341,RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_85489,RMVar_hsa_circ_78811,RMVar_hsa_circ_135609,RMVar_hsa_circ_135612,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_135614,RMVar_hsa_circ_64344,RMVar_hsa_circ_26648,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_104205,RMVar_hsa_circ_135617,RMVar_hsa_circ_135618,RMVar_hsa_circ_135620,RMVar_hsa_circ_135619,RMVar_hsa_circ_371218,RMVar_hsa_circ_112954,RMVar_hsa_circ_5028,RMVar_hsa_circ_135621 71251 RMVar_ID_71251 Human_SNP_ID_28998734 m1A Human chr1 + 116393562 116393547 116393563 GTTGTCTATTCATAAGAACCCCAACACATCGGAGCCCCAACACCTGTTGGTGATGAAGGGCGCCC GTTGTCTATTCATAAGAA________________CCCCAACACCTGTTGGTGATGAAGGGCGCCC ACCCCAACACATCGGAG A ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:116393547..116393663 26863196 MeRIP-seq:(Medium) rs775427851 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_22802,Human_RBP_ID_857871,Human_RBP_ID_1409252,Human_RBP_ID_1723218,Human_RBP_ID_3984953,Human_RBP_ID_8282166,Human_RBP_ID_8755087,Human_RBP_ID_17211622,Human_RBP_ID_17668358,Human_RBP_ID_18187783,Human_RBP_ID_18204461,Human_RBP_ID_22427406,Human_RBP_ID_22532139,Human_RBP_ID_22749379,Human_RBP_ID_23205301,Human_RBP_ID_26798729,Human_RBP_ID_27386393 Human_Splice_Rec_113832,Human_Splice_Rec_113880,Human_Splice_Rec_113934 Human_miRNA_ID_2889184 RMVar_hsa_circ_12349,RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_85489,RMVar_hsa_circ_78811,RMVar_hsa_circ_135609,RMVar_hsa_circ_135612,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_135614,RMVar_hsa_circ_64344,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_104205,RMVar_hsa_circ_135617,RMVar_hsa_circ_135618,RMVar_hsa_circ_135619,RMVar_hsa_circ_112954,RMVar_hsa_circ_69417,RMVar_hsa_circ_5028,RMVar_hsa_circ_135621,RMVar_hsa_circ_109389,RMVar_hsa_circ_135622 71252 RMVar_ID_71252 Human_SNP_ID_28999532 m1A Human chr1 - 116396693 116396693 116396693 ACCTGGCTGACTGGGATGTTGAGGCGGGCAGCAATGTCTTCCACGGTCTCATTGCCTTCTGAGAT ACCTGGCTGACTGGGATGTTGAGGCGGGCAGCGATGTCTTCCACGGTCTCATTGCCTTCTGAGAT T C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:116396644..116396775 26863196 MeRIP-seq:(Medium) rs1322155213 Functional Loss SNV dbSNP153 33..33 33 - - - 71253 RMVar_ID_71253 Human_SNP_ID_29000077 m1A Human chr1 + 116399026 116399026 116399026 GATCACCCCGTTCCTGATATTTATTATTGCAAACATTCCACTACCACTGGGGACTGTCACCATCC GATCACCCCGTTCCTGATATTTATTATTGCAAGCATTCCACTACCACTGGGGACTGTCACCATCC A G ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:116399001..116399025 26863196 MeRIP-seq:(Medium) rs1367224721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22813,Human_RBP_ID_1148912,Human_RBP_ID_1344327,Human_RBP_ID_1723238,Human_RBP_ID_2088600,Human_RBP_ID_3278022,Human_RBP_ID_5677058,Human_RBP_ID_8043039,Human_RBP_ID_8282189,Human_RBP_ID_8733325,Human_RBP_ID_8954544,Human_RBP_ID_9251827,Human_RBP_ID_9266127,Human_RBP_ID_17211633,Human_RBP_ID_17329608,Human_RBP_ID_17445231,Human_RBP_ID_17722571,Human_RBP_ID_18187234,Human_RBP_ID_22429589,Human_RBP_ID_22749392,Human_RBP_ID_22779280,Human_RBP_ID_23325856,Human_RBP_ID_24446637,Human_RBP_ID_26577332,Human_RBP_ID_26798736,Human_RBP_ID_26838587,Human_RBP_ID_27152690,Human_RBP_ID_27386403,Human_RBP_ID_27577298 Human_Splice_Rec_113842,Human_Splice_Rec_113843,Human_Splice_Rec_113890,Human_Splice_Rec_113891,Human_Splice_Rec_113944,Human_Splice_Rec_113945 Human_miRNA_ID_1932704,Human_miRNA_ID_2196512,Human_miRNA_ID_2643986,Human_miRNA_ID_2935522 RMVar_hsa_circ_352627,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_64344,RMVar_hsa_circ_20747,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_135618,RMVar_hsa_circ_135619,RMVar_hsa_circ_112954,RMVar_hsa_circ_135621,RMVar_hsa_circ_109389,RMVar_hsa_circ_79272,RMVar_hsa_circ_135622,RMVar_hsa_circ_135623,RMVar_hsa_circ_91455,RMVar_hsa_circ_46788,RMVar_hsa_circ_318923,RMVar_hsa_circ_135626 71254 RMVar_ID_71254 Human_SNP_ID_29000088 m1A Human chr1 + 116399068 116399068 116399068 ACCACTGGGGACTGTCACCATCCTCTGCATTGACTTGGGCACTGACATGGTGAGTGTCACAACAG ACCACTGGGGACTGTCACCATCCTCTGCATTGCCTTGGGCACTGACATGGTGAGTGTCACAACAG A C ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1553192783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744047,Human_RBP_ID_857882,Human_RBP_ID_1148913,Human_RBP_ID_9270288,Human_RBP_ID_10539972,Human_RBP_ID_17221541,Human_RBP_ID_17338349,Human_RBP_ID_17456286,Human_RBP_ID_18187234,Human_RBP_ID_22125385,Human_RBP_ID_22427410,Human_RBP_ID_22749392,Human_RBP_ID_26798739 Human_Splice_Rec_113843,Human_Splice_Rec_113891,Human_Splice_Rec_113945 Clinvar_Rec_296,Clinvar_Rec_2565 GWAS_ID_8447 RMVar_hsa_circ_352627,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_64344,RMVar_hsa_circ_20747,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_135618,RMVar_hsa_circ_135619,RMVar_hsa_circ_112954,RMVar_hsa_circ_135621,RMVar_hsa_circ_109389,RMVar_hsa_circ_79272,RMVar_hsa_circ_135622,RMVar_hsa_circ_135623,RMVar_hsa_circ_91455,RMVar_hsa_circ_46788,RMVar_hsa_circ_318923,RMVar_hsa_circ_135626 71255 RMVar_ID_71255 Human_SNP_ID_29001313 m1A Human chr1 - 116403955 116403955 116403955 GCCCATAATTACCGCCAGGGCGTCGCCTGATGATGAGTTTTCTGACTTCGTCATATACGAAGATG GCCCATAATTACCGCCAGGGCGTCGCCTGATGTTGAGTTTTCTGACTTCGTCATATACGAAGATG T A ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:116403905..116404475 32194978 MeRIP-seq:(Medium) rs1440360198 Functional Loss SNV dbSNP153 33..33 33 - - - 71256 RMVar_ID_71256 Human_SNP_ID_29001422 m1A Human chr1 - 116404402 116404401 116404403 GTTTCCTTCTCCACCCAGCCTGTGGGTGGCAAAGAGACAGACAAGACACACTACAGTGAGTCTTC GTTTCCTTCTCCACCCAGCCTGTGGGTGGCA__GAGACAGACAAGACACACTACAGTGAGTCTTC CTT C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116404401..116404450 26863196 MeRIP-seq:(Medium) rs1557797354 Functional Loss DEL dbSNP153 32..33 33 - - - 71257 RMVar_ID_71257 Human_SNP_ID_29001424 m1A Human chr1 - 116404402 116404402 116404402 GTTTCCTTCTCCACCCAGCCTGTGGGTGGCAAAGAGACAGACAAGACACACTACAGTGAGTCTTC GTTTCCTTCTCCACCCAGCCTGTGGGTGGCAAGGAGACAGACAAGACACACTACAGTGAGTCTTC T C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116404401..116404450 26863196 MeRIP-seq:(Medium) rs1238829832 Functional Loss SNV dbSNP153 33..33 33 - - - 71258 RMVar_ID_71258 Human_SNP_ID_29001479 m1A Human chr1 - 116404522 116404522 116404522 TTTCCTACCAGGGTAGAGTTCCAAACTCCAAGACTGAAGTACACAAAGAGGGGGTGGGTGTCGGA TTTCCTACCAGGGTAGAGTTCCAAACTCCAAGGCTGAAGTACACAAAGAGGGGGTGGGTGTCGGA T C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116404471..116404575 26863196 MeRIP-seq:(Medium) rs946904003 Functional Loss SNV dbSNP153 33..33 33 - - - 71259 RMVar_ID_71259 Human_SNP_ID_29002136 m1A Human chr1 - 116407011 116407008 116407012 GAGCTAAGGAGTGCACAGAGACAATGACAGAAAGACGGGAGGTCTGGTTTCAGGAAGGGTGTGAT GAGCTAAGGAGTGCACAGAGACAATGACAGA____CGGGAGGTCTGGTTTCAGGAAGGGTGTGAT GTCTT G ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116406960..116407106 26863196 MeRIP-seq:(Medium) rs962387376 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5677090 Human_Splice_Rec_113989 71260 RMVar_ID_71260 Human_SNP_ID_29002139 m1A Human chr1 - 116407011 116407011 116407011 GAGCTAAGGAGTGCACAGAGACAATGACAGAAAGACGGGAGGTCTGGTTTCAGGAAGGGTGTGAT GAGCTAAGGAGTGCACAGAGACAATGACAGAAGGACGGGAGGTCTGGTTTCAGGAAGGGTGTGAT T C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116406960..116407106 26863196 MeRIP-seq:(Medium) rs1281202682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5677090 Human_Splice_Rec_113989 71261 RMVar_ID_71261 Human_SNP_ID_29002144 m1A Human chr1 - 116407027 116407026 116407028 GTGAAGAGGGGGCTGAGAGCTAAGGAGTGCACAGAGACAATGACAGAAAGACGGGAGGTCTGGTT GTGAAGAGGGGGCTGAGAGCTAAGGAGTGCA__GAGACAATGACAGAAAGACGGGAGGTCTGGTT CTG C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:116406984..116407089 26863196 MeRIP-seq:(Medium) rs1436728820 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5540494,Human_RBP_ID_5892615 Human_Splice_Rec_113989 71262 RMVar_ID_71262 Human_SNP_ID_29028625 m1A Human chr1 - 116515632 116515631 116515632 GATTCCTTGTAGTGGGTGAGGAGACTGCTGGGAGAGGGCAGGGAAGCAGAGACCGGCAAAAAGCT GATTCCTTGTAGTGGGTGAGGAGACTGCTGGG_GAGGGCAGGGAAGCAGAGACCGGCAAAAAGCT CT C CD58 Ensembl:ENSG00000116815 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:116515584..116515684 26863196 MeRIP-seq:(Medium) rs914421728 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24358467 RMVar_hsa_circ_127652,RMVar_hsa_circ_135629 71263 RMVar_ID_71263 Human_SNP_ID_29029214 m1A Human chr1 - 116518578 116518576 116518579 TTAAGGCCCAGGGTGTGAAGGGCAGGACAAGAAGTAGCAAGCCATCCTCTTTGGAGCAGAGAGTG TTAAGGCCCAGGGTGTGAAGGGCAGGACAAG___TAGCAAGCCATCCTCTTTGGAGCAGAGAGTG ACTT A CD58 Ensembl:ENSG00000116815 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:116518407..116518638 26863196 MeRIP-seq:(Medium) rs774726769 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_127652,RMVar_hsa_circ_135629 71264 RMVar_ID_71264 Human_SNP_ID_29040394 m1A Human chr1 + 116570964 116570964 116570964 AGGACCCCCAGGGCCCGCCCCGCGTCGCTCCCAGCAACCATGGCTCGTCGGGCCGGCCTCTGCGC AGGACCCCCAGGGCCCGCCCCGCGTCGCTCCCTGCAACCATGGCTCGTCGGGCCGGCCTCTGCGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116570758..116570965 26863196 MeRIP-seq:(Medium) rs765705276 Functional Loss SNV dbSNP153 33..33 33 - - - 71265 RMVar_ID_71265 Human_SNP_ID_29040395 m1A Human chr1 + 116570967 116570967 116570967 ACCCCCAGGGCCCGCCCCGCGTCGCTCCCAGCAACCATGGCTCGTCGGGCCGGCCTCTGCGCGAG ACCCCCAGGGCCCGCCCCGCGTCGCTCCCAGCTACCATGGCTCGTCGGGCCGGCCTCTGCGCGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116570759..116571008 26863196 MeRIP-seq:(Medium) rs753087323 Functional Loss SNV dbSNP153 33..33 33 - - - 71266 RMVar_ID_71266 Human_SNP_ID_29062343 m1A Human chr1 + 116667667 116667667 116667667 CCCTCCGCGCGCGTCGGACCGTCCTTCAGTCCATCCAGGCGCACGCCTCAGGGGACGCGCCGCTT CCCTCCGCGCGCGTCGGACCGTCCTTCAGTCCTTCCAGGCGCACGCCTCAGGGGACGCGCCGCTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:116667572..116667709;chr1:116667574..116667745 26863196 MeRIP-seq:(Medium) rs1414680574 Functional Loss SNV dbSNP153 33..33 33 - - - 71267 RMVar_ID_71267 Human_SNP_ID_29062355 m1A Human chr1 - 116667705 116667705 116667705 CCGCAGCGCGGCTGCTGGTGCCGTTGCGGGAGAAGAGGAAGCGGCGCGTCCCCTGAGGCGTGCGC CCGCAGCGCGGCTGCTGGTGCCGTTGCGGGAGGAGAGGAAGCGGCGCGTCCCCTGAGGCGTGCGC T C IGSF3 Ensembl:ENSG00000143061 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116667559..116667756 26863196 MeRIP-seq:(Medium) rs570856019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224031,Human_RBP_ID_4079403 Human_Splice_Rec_114071,Human_Splice_Rec_114093 71268 RMVar_ID_71268 Human_SNP_ID_29062358 m1A Human chr1 - 116667707 116667707 116667707 GGCCGCAGCGCGGCTGCTGGTGCCGTTGCGGGAGAAGAGGAAGCGGCGCGTCCCCTGAGGCGTGC GGCCGCAGCGCGGCTGCTGGTGCCGTTGCGGGGGAAGAGGAAGCGGCGCGTCCCCTGAGGCGTGC T C IGSF3 Ensembl:ENSG00000143061 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116667576..116667797 26863196 MeRIP-seq:(Medium) rs1330834983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224031 Human_Splice_Rec_114071,Human_Splice_Rec_114093 71269 RMVar_ID_71269 Human_SNP_ID_29122870 m1A Human chr1 - 116910054 116910054 116910054 TGCTCCGCTCTCCTCGCGAGCCGATAAATCCCAGCGCTGGGGCGTACGTGCGCCCCTGGCTCCGC TGCTCCGCTCTCCTCGCGAGCCGATAAATCCCTGCGCTGGGGCGTACGTGCGCCCCTGGCTCCGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:116909923..116910146 26863196 MeRIP-seq:(Medium) rs1039925477 Functional Loss SNV dbSNP153 33..33 33 - - - 71270 RMVar_ID_71270 Human_SNP_ID_29130264 m1A Human chr1 - 116941769 116941769 116941769 TGACGTTGCAGGGGATGACCAGCTCAGTGCCCACCACTCGAACCAGGGTCGCTGTGGGGACTCTC TGACGTTGCAGGGGATGACCAGCTCAGTGCCCGCCACTCGAACCAGGGTCGCTGTGGGGACTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:116941685..116941793 26863196 MeRIP-seq:(Medium) rs1469959312 Functional Loss SNV dbSNP153 33..33 33 - - - 71271 RMVar_ID_71271 Human_SNP_ID_29131121 m1A Human chr1 + 116945002 116945002 116945002 CTCTGTCTGCCGACCAGGGCTCCTACAGGTGTATCGTCAGCGAGTGGATCGCCGAGCAGGGCAAC CTCTGTCTGCCGACCAGGGCTCCTACAGGTGTGTCGTCAGCGAGTGGATCGCCGAGCAGGGCAAC A G PTGFRN Ensembl:ENSG00000134247 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:116941766..116945007 32194978 MeRIP-seq:(Medium) rs549841982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3985426 Human_Splice_Rec_114155 RMVar_hsa_circ_79939,RMVar_hsa_circ_73827,RMVar_hsa_circ_297088,RMVar_hsa_circ_135638,RMVar_hsa_circ_83017,RMVar_hsa_circ_85791,RMVar_hsa_circ_38706,RMVar_hsa_circ_135639,RMVar_hsa_circ_135640 71272 RMVar_ID_71272 Human_SNP_ID_29159219 m1A Human chr1 + 117060345 117060345 117060345 GCGGGGCTTTGTGGAACTTGGGGGACCCAGCGAAATGGAAGAAGTTAGGTGTCCAGAGCACGGTA GCGGGGCTTTGTGGAACTTGGGGGACCCAGCGGAATGGAAGAAGTTAGGTGTCCAGAGCACGGTA A G TTF2 Ensembl:ENSG00000116830 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:117060326..117060481 26863410 MeRIP-seq:(Medium) rs1165469405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9452162 Human_Splice_Rec_114219,Human_Splice_Rec_114263 RMVar_hsa_circ_100664,RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135647 71273 RMVar_ID_71273 Human_SNP_ID_29159246 m1A Human chr1 + 117060372 117060372 117060372 CAGCGAAATGGAAGAAGTTAGGTGTCCAGAGCACGGTAAGGGGCTAGGGTCTCAGCGTCCCGGGG CAGCGAAATGGAAGAAGTTAGGTGTCCAGAGCGCGGTAAGGGGCTAGGGTCTCAGCGTCCCGGGG A G TTF2 Ensembl:ENSG00000116830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:117060333..117060533;chr1:117060340..117060508;chr1:117060342..117060526 26863196 MeRIP-seq:(Medium) rs754722173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5331866,Human_RBP_ID_19038916 Human_Splice_Rec_114219,Human_Splice_Rec_114263 RMVar_hsa_circ_100664,RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135647 71274 RMVar_ID_71274 Human_SNP_ID_29159342 m1A Human chr1 + 117060579 117060579 117060579 CGGGCCACCGAGTAGGTCTGGAGCTGGGCCCCACTCCCTGTGGCTGCCCGGGGCCTCCCGAGAGG CGGGCCACCGAGTAGGTCTGGAGCTGGGCCCCGCTCCCTGTGGCTGCCCGGGGCCTCCCGAGAGG A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:117060532..117060674 26863196 MeRIP-seq:(Medium) rs780863429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5338263 RMVar_hsa_circ_100664,RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135647,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212 71275 RMVar_ID_71275 Human_SNP_ID_29169522 m1A Human chr1 + 117103122 117103122 117103122 GAAGATTACAAGGCCCTAGGGAAGGTGAAGCCACTAGCTCAGCAGTTCTTAGCCTAGTTTTTGGC GAAGATTACAAGGCCCTAGGGAAGGTGAAGCCGCTAGCTCAGCAGTTCTTAGCCTAGTTTTTGGC A G TTF2 Ensembl:ENSG00000116830 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9728670 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8448,GWAS_ID_8449 71276 RMVar_ID_71276 Human_SNP_ID_29173931 m1A Human chr1 - 117121238 117121238 117121238 TAATCACCTGCTACTAAATCGTAGAACTGCCCAGGGCCCTTTCTAATATTGGTCACAAACGTGAG TAATCACCTGCTACTAAATCGTAGAACTGCCCGGGGCCCTTTCTAATATTGGTCACAAACGTGAG T C TRIM45 Ensembl:ENSG00000134253 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:117121190..117121291 26863196 MeRIP-seq:(Medium) rs1449634237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10542250,Human_RBP_ID_18548735,Human_RBP_ID_26838843 71277 RMVar_ID_71277 Human_SNP_ID_29174056 m1A Human chr1 - 117121694 117121694 117121694 GCCGAGGCGCGGGAGAGGCGGTGGACACCGAGAAGCCCGCCGGCGGCTTGCAATTCCCTCACCCG GCCGAGGCGCGGGAGAGGCGGTGGACACCGAGGAGCCCGCCGGCGGCTTGCAATTCCCTCACCCG T C TRIM45 Ensembl:ENSG00000134253 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:117121567..117121693 26863196 MeRIP-seq:(Medium) rs1290063228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_114341 71278 RMVar_ID_71278 Human_SNP_ID_29233701 m1A Human chr1 + 117366916 117366916 117366916 TCGCCCCCGCCCTCCGGTTCCTCTCCGGCGTGAGCCCAACGGGTGTCGGCCCAGCAGCTGCTGCG TCGCCCCCGCCCTCCGGTTCCTCTCCGGCGTGGGCCCAACGGGTGTCGGCCCAGCAGCTGCTGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:117366866..117367231 26863196 MeRIP-seq:(Medium) rs999437696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8954604,Human_RBP_ID_26838849 71279 RMVar_ID_71279 Human_SNP_ID_29242338 m1A Human chr1 + 117402292 117402292 117402292 TAAGAAAGTCAAGAGAGGAAATTCGAGCAGAAATTCAGACAGAGAAAAATAAGGTAGTCCAAGAA TAAGAAAGTCAAGAGAGGAAATTCGAGCAGAAGTTCAGACAGAGAAAAATAAGGTAGTCCAAGAA A G MAN1A2 Ensembl:ENSG00000198162 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:117402242..117402313 26863196 MeRIP-seq:(Medium) rs1283135548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_860460,Human_RBP_ID_2089138,Human_RBP_ID_10542461,Human_RBP_ID_18428330,Human_RBP_ID_22026435,Human_RBP_ID_22845381,Human_RBP_ID_26311668,Human_RBP_ID_26838880 RMVar_hsa_circ_116005,RMVar_hsa_circ_94822,RMVar_hsa_circ_126555,RMVar_hsa_circ_135674,RMVar_hsa_circ_135671,RMVar_hsa_circ_135672,RMVar_hsa_circ_135673,RMVar_hsa_circ_270808,RMVar_hsa_circ_279180,RMVar_hsa_circ_296312,RMVar_hsa_circ_372551,RMVar_hsa_circ_295063,RMVar_hsa_circ_276586,RMVar_hsa_circ_270277,RMVar_hsa_circ_135678,RMVar_hsa_circ_135680,RMVar_hsa_circ_135682,RMVar_hsa_circ_95574,RMVar_hsa_circ_135683,RMVar_hsa_circ_135681,RMVar_hsa_circ_135679,RMVar_hsa_circ_135676,RMVar_hsa_circ_135677,RMVar_hsa_circ_135675 71280 RMVar_ID_71280 Human_SNP_ID_29289368 m1A Human chr1 - 117606131 117606131 117606131 GCGGACTCACCTGGGCAATAGAAGAGGAGGCGACAGAGGCAGGTCCTTGGCGTGGGCAGGCCCCA GCGGACTCACCTGGGCAATAGAAGAGGAGGCGGCAGAGGCAGGTCCTTGGCGTGGGCAGGCCCCA T C LOC100996263 RNACentral:URS00009C40EF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:117606084..117606178 26863196 MeRIP-seq:(Medium) rs976128201 Functional Loss SNV dbSNP153 33..33 33 - - - 71281 RMVar_ID_71281 Human_SNP_ID_29366128 m1A Human chr1 + 117929815 117929815 117929815 GTGAGTCCTGGAGGTGCGTGGTTGGGGCGGAGAGCATTATCTGCGGCTCCGATTTTGCAGATTCT GTGAGTCCTGGAGGTGCGTGGTTGGGGCGGAGGGCATTATCTGCGGCTCCGATTTTGCAGATTCT A G WDR3 Ensembl:ENSG00000065183 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:117929789..117929882 26863196 MeRIP-seq:(Medium) rs921834654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074321 71282 RMVar_ID_71282 Human_SNP_ID_29644760 m1A Human chr1 + 119033140 119033140 119033140 CCGCGCTGCGGCGCACCACTTCCTCCACGGAGAGCCCCGTCACCGCGGCATGCACCGCCACTATG CCGCGCTGCGGCGCACCACTTCCTCCACGGAGCGCCCCGTCACCGCGGCATGCACCGCCACTATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119033092..119033220 26863196 MeRIP-seq:(Medium) rs1270429647 Functional Loss SNV dbSNP153 33..33 33 - - - 71283 RMVar_ID_71283 Human_SNP_ID_29668619 m1A Human chr1 - 119140454 119140454 119140454 TATTTATTTCTCTCCTCCCGCTTCTTAGGGAAAGTACATGCCTTCCCTCGCCTAAGGTCTACTCG TATTTATTTCTCTCCTCCCGCTTCTTAGGGAAGGTACATGCCTTCCCTCGCCTAAGGTCTACTCG T C WARS2 Ensembl:ENSG00000116874 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:119140401..119140625 26863196 MeRIP-seq:(Medium) rs1201451909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_114920 RMVar_hsa_circ_122520,RMVar_hsa_circ_135728 71284 RMVar_ID_71284 Human_SNP_ID_29668623 m1A Human chr1 + 119140480 119140477 119140481 ATGTACTTTCCCTAAGAAGCGGGAGGAGAGAAATAAATAGAGGGCAGTGGGATGAGAAGAACCTC ATGTACTTTCCCTAAGAAGCGGGAGGAGAG____AAATAGAGGGCAGTGGGATGAGAAGAACCTC GAAAT G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:119140426..119140567 26863196 MeRIP-seq:(Medium) rs999392441 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4079690,Human_RBP_ID_5541068,Human_RBP_ID_18415034,Human_RBP_ID_21963137,Human_RBP_ID_22026436,Human_RBP_ID_26314569 71285 RMVar_ID_71285 Human_SNP_ID_29678877 m1A Human chr1 + 119177814 119177813 119177814 AGACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGA AGACAGAGAAAGAGACAGAGAGAGGAAGAAAC_GAGAGTCAAAGAGAAAGAGACAAAGAGAAGGA CA C WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:119177724..119177884 26863196 MeRIP-seq:(Medium) rs768732833 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 71286 RMVar_ID_71286 Human_SNP_ID_29678878 m1A Human chr1 + 119177816 119177813 119177817 ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT ACAGAGAAAGAGACAGAGAGAGGAAGAAAC____AGTCAAAGAGAAAGAGACAAAGAGAAGGAGT CAGAG C WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119177716..119177863 26863196 MeRIP-seq:(Medium) rs751011309 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 71287 RMVar_ID_71287 Human_SNP_ID_29678879 m1A Human chr1 + 119177816 119177813 119177817 ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT ACAGAGAAAGAGACAGAGAGAGGAAGAAACAG__AGTCAAAGAGAAAGAGACAAAGAGAAGGAGT CAGAG CAG WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119177716..119177863 26863196 MeRIP-seq:(Medium) rs751011309 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 71288 RMVar_ID_71288 Human_SNP_ID_29678880 m1A Human chr1 + 119177816 119177815 119177816 ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT ACAGAGAAAGAGACAGAGAGAGGAAGAAACAG_GAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT GA G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119177716..119177863 26863196 MeRIP-seq:(Medium) rs778259821 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 71289 RMVar_ID_71289 Human_SNP_ID_29678881 m1A Human chr1 + 119177816 119177816 119177816 ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGGGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119177716..119177863 26863196 MeRIP-seq:(Medium) rs12067751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 71290 RMVar_ID_71290 Human_SNP_ID_29794394 m1A Human chr1 + 119623809 119623809 119623809 GTGGGCGCGTCCATGATGCTGGCCACCAGGCTATCCAGCTCCCCGAGGTCCACGGCCATGGGGTG GTGGGCGCGTCCATGATGCTGGCCACCAGGCTCTCCAGCTCCCCGAGGTCCACGGCCATGGGGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:119623758..119623859 32194978 MeRIP-seq:(Medium) rs761854503 Functional Loss SNV dbSNP153 33..33 33 - - - 71291 RMVar_ID_71291 Human_SNP_ID_29794494 m1A Human chr1 + 119623971 119623971 119623971 TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCAGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCGGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119623923..119624034 26863196 MeRIP-seq:(Medium) rs772380695 Functional Loss SNV dbSNP153 33..33 33 - - - 71292 RMVar_ID_71292 Human_SNP_ID_29794495 m1A Human chr1 + 119623971 119623971 119623971 TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCAGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCTGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119623923..119624034 26863196 MeRIP-seq:(Medium) rs772380695 Functional Loss SNV dbSNP153 33..33 33 - - - 71293 RMVar_ID_71293 Human_SNP_ID_29796521 m1A Human chr1 + 119631744 119631744 119631744 GGGGAAGGAAGCGGCCCGGCGGGCGGCGGGCCAGGAGCGGCTCCCACTCGGGCCTCCAGACTGCA GGGGAAGGAAGCGGCCCGGCGGGCGGCGGGCCGGGAGCGGCTCCCACTCGGGCCTCCAGACTGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:119631660..119631787 26863196 MeRIP-seq:(Medium) rs1419398056 Functional Loss SNV dbSNP153 33..33 33 - - - 71294 RMVar_ID_71294 Human_SNP_ID_29796522 m1A Human chr1 + 119631744 119631744 119631744 GGGGAAGGAAGCGGCCCGGCGGGCGGCGGGCCAGGAGCGGCTCCCACTCGGGCCTCCAGACTGCA GGGGAAGGAAGCGGCCCGGCGGGCGGCGGGCCTGGAGCGGCTCCCACTCGGGCCTCCAGACTGCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:119631660..119631787 26863196 MeRIP-seq:(Medium) rs1419398056 Functional Loss SNV dbSNP153 33..33 33 - - - 71295 RMVar_ID_71295 Human_SNP_ID_29815347 m1A Human chr1 - 119712003 119711993 119712003 TTGCAAAAGCCATTGCTGGAGTTGGCCTCGGAATCGGCCGCTGTGAGTAGAAGTACCTAAGCCAA TTGCAAAAGCCATTGCTGGAGTTGGCCTCGGA__________GTGAGTAGAAGTACCTAAGCCAA CAGCGGCCGAT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:119711901..119712075 26863410 MeRIP-seq:(Medium) rs1557961814 Functional Loss DEL dbSNP153 33..42 33 - - - 71296 RMVar_ID_71296 Human_SNP_ID_29815828 m1A Human chr1 - 119713678 119713678 119713678 AGAGCCACTGATACAATTTCACACAAGAAAGGAGGTGACAGATGTGAGGAGCCTGCCACCCGTCC AGAGCCACTGATACAATTTCACACAAGAAAGGCGGTGACAGATGTGAGGAGCCTGCCACCCGTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:119713676..119714032 26863196 MeRIP-seq:(Medium) rs1012059183 Functional Loss SNV dbSNP153 33..33 33 - - - 71297 RMVar_ID_71297 Human_SNP_ID_29816086 m1A Human chr1 + 119714727 119714727 119714727 CCTGTCTCTACAAAAAATACGAACATTAGCTAAGCATCTTGCACAAGCCTGTAGTCTCAGCTACT CCTGTCTCTACAAAAAATACGAACATTAGCTACGCATCTTGCACAAGCCTGTAGTCTCAGCTACT A C PHGDH Ensembl:ENSG00000092621 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:119714722..119714840 26863196 MeRIP-seq:(Medium) rs1204115517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10549744 RMVar_hsa_circ_85093,RMVar_hsa_circ_135736 71298 RMVar_ID_71298 Human_SNP_ID_29817554 m1A Human chr1 - 119721283 119721269 119721284 ACCAAGATGCCCTTCCTTGTTGCGGCCTCCAGATCCACATTGTCCACACCTGTGCCAGCCCTGCC ACCAAGATGCCCTTCCTTGTTGCGGCCTCCA_______________CACCTGTGCCAGCCCTGCC GTGGACAATGTGGATC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:119721233..119721399 26863196 MeRIP-seq:(Medium) rs1254451152 Functional Loss DEL dbSNP153 32..46 33 - - - 71299 RMVar_ID_71299 Human_SNP_ID_29819070 m1A Human chr1 + 119726931 119726931 119726931 GAAGAAGGTGAGCAGCGGCCTTGACTCGCCCCACCTGGGCTCAGGGCCCGGGGTCCACTCATGTT GAAGAAGGTGAGCAGCGGCCTTGACTCGCCCCCCCTGGGCTCAGGGCCCGGGGTCCACTCATGTT A C PHGDH Ensembl:ENSG00000092621 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:119726924..119727009 26863196 MeRIP-seq:(Medium) rs752274687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22414082,Human_RBP_ID_22638815 Human_Splice_Rec_115140,Human_Splice_Rec_115164,Human_Splice_Rec_115178,Human_Splice_Rec_115200,Human_Splice_Rec_115208,Human_Splice_Rec_115232,Human_Splice_Rec_115254,Human_Splice_Rec_115278,Human_Splice_Rec_115296,Human_Splice_Rec_115318,Human_Splice_Rec_115330,Human_Splice_Rec_115356,Human_Splice_Rec_115362,Human_Splice_Rec_115370,Human_Splice_Rec_115382,Human_Splice_Rec_115396,Human_Splice_Rec_115422,Human_Splice_Rec_115444,Human_Splice_Rec_115456,Human_Splice_Rec_115466,Human_Splice_Rec_115476,Human_Splice_Rec_115494,Human_Splice_Rec_115516,Human_Splice_Rec_115524,Human_Splice_Rec_115546,Human_Splice_Rec_115566,Human_Splice_Rec_115586 RMVar_hsa_circ_101990,RMVar_hsa_circ_58249,RMVar_hsa_circ_79460,RMVar_hsa_circ_135737,RMVar_hsa_circ_97964,RMVar_hsa_circ_135738,RMVar_hsa_circ_135739,RMVar_hsa_circ_48179 71300 RMVar_ID_71300 Human_SNP_ID_29819233 m1A Human chr1 - 119727433 119727433 119727433 AATATTCTTTTTCCTTTGCAATAAACTCCTCAATGCTGCACCGTGTCTCTTGTTTAAATTCTTTT AATATTCTTTTTCCTTTGCAATAAACTCCTCAGTGCTGCACCGTGTCTCTTGTTTAAATTCTTTT T C lnc-HMGCS2-1 RNACentral:URS0000D59F6B lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:119727428..119727581 26863196 MeRIP-seq:(Medium) rs939753751 Functional Loss SNV dbSNP153 33..33 33 - - - 71301 RMVar_ID_71301 Human_SNP_ID_29821853 m1A Human chr1 + 119737235 119737235 119737235 CTGTGGGGAGGAAATTGCTGTTCAGTTCGTGGACATGGTGAAGGGGAAATCTCTCACGGGGGTTG CTGTGGGGAGGAAATTGCTGTTCAGTTCGTGGCCATGGTGAAGGGGAAATCTCTCACGGGGGTTG A C PHGDH Ensembl:ENSG00000092621 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:119737063..119737302 26863196 MeRIP-seq:(Medium) rs773652124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745969,Human_RBP_ID_970483,Human_RBP_ID_1249716,Human_RBP_ID_1409751,Human_RBP_ID_8282959,Human_RBP_ID_8733698,Human_RBP_ID_8954828,Human_RBP_ID_10550668,Human_RBP_ID_17762830,Human_RBP_ID_18549210,Human_RBP_ID_18965874,Human_RBP_ID_22429614 Human_Splice_Rec_115149,Human_Splice_Rec_115187,Human_Splice_Rec_115217,Human_Splice_Rec_115241,Human_Splice_Rec_115263,Human_Splice_Rec_115287,Human_Splice_Rec_115305,Human_Splice_Rec_115339,Human_Splice_Rec_115405,Human_Splice_Rec_115431,Human_Splice_Rec_115503,Human_Splice_Rec_115533,Human_Splice_Rec_115555,Human_Splice_Rec_115575,Human_Splice_Rec_115595,Human_Splice_Rec_115607 RMVar_hsa_circ_101990,RMVar_hsa_circ_135737,RMVar_hsa_circ_329829,RMVar_hsa_circ_371907,RMVar_hsa_circ_135741 71302 RMVar_ID_71302 Human_SNP_ID_29823391 m1A Human chr1 + 119743026 119743026 119743026 TCCTATTCCGGACTCAGACCTCTGACCCTGCAATGCTGCCTACCATGATTGGTGAGGAGGGCCCT TCCTATTCCGGACTCAGACCTCTGACCCTGCAGTGCTGCCTACCATGATTGGTGAGGAGGGCCCT A G PHGDH Ensembl:ENSG00000092621 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:119742783..119743086 26863196 MeRIP-seq:(Medium) rs1249140637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271733,Human_RBP_ID_323566,Human_RBP_ID_5108720,Human_RBP_ID_5484139,Human_RBP_ID_5680477,Human_RBP_ID_8282971,Human_RBP_ID_10550863,Human_RBP_ID_17338360,Human_RBP_ID_18549227,Human_RBP_ID_22427440,Human_RBP_ID_22750265,Human_RBP_ID_27386796 Human_Splice_Rec_115155,Human_Splice_Rec_115193,Human_Splice_Rec_115223,Human_Splice_Rec_115247,Human_Splice_Rec_115267,Human_Splice_Rec_115289,Human_Splice_Rec_115309,Human_Splice_Rec_115345,Human_Splice_Rec_115411,Human_Splice_Rec_115437,Human_Splice_Rec_115509,Human_Splice_Rec_115539,Human_Splice_Rec_115561,Human_Splice_Rec_115581,Human_Splice_Rec_115617 Human_miRNA_ID_39697,Human_miRNA_ID_68414,Human_miRNA_ID_1935923,Human_miRNA_ID_1947023,Human_miRNA_ID_2275937 RMVar_hsa_circ_121997,RMVar_hsa_circ_135742,RMVar_hsa_circ_269099 71303 RMVar_ID_71303 Human_SNP_ID_29823651 m1A Human chr1 - 119744067 119744067 119744067 TCACAGTGGGTGGGTTTCTTCAGAAAAGCCCCAGAGGCAGGGACCAGTGAGCTCCAAGGTTAGAA TCACAGTGGGTGGGTTTCTTCAGAAAAGCCCCGGAGGCAGGGACCAGTGAGCTCCAAGGTTAGAA T C lnc-HMGCS2-1,lnc-HMGCS2-1:2 RNACentral:URS0000D59F6B,RNACentral:URS0000D5BF49 lincRNA,lincRNA exon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:119744026..119744125 26863196 MeRIP-seq:(Medium) rs1292895094 Functional Loss SNV dbSNP153 33..33 33 - - - 71304 RMVar_ID_71304 Human_SNP_ID_29867261 m1A Human chr1 - 119913175 119913175 119913175 CTCCATGTGGCAACATTCTGTCAGCCTCTTTCATAGTGTGCAAACATTTTATCATTCTAAATGGT CTCCATGTGGCAACATTCTGTCAGCCTCTTTCGTAGTGTGCAAACATTTTATCATTCTAAATGGT T C NOTCH2 Ensembl:ENSG00000134250 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:119912948..119913249 32194978 MeRIP-seq:(Medium) rs370678356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1149039,Human_RBP_ID_17211788,Human_RBP_ID_17723504,Human_RBP_ID_18215919,Human_RBP_ID_19151272,Human_RBP_ID_22373276,Human_RBP_ID_23327407,Human_RBP_ID_27577698 Human_miRNA_ID_848773,Human_miRNA_ID_1404673 RMVar_hsa_circ_269815 71305 RMVar_ID_71305 Human_SNP_ID_29867776 m1A Human chr1 + 119915459 119915459 119915459 GAGTGGGGTGATGAACTTGACCACTGGTCAGGAGACTCTGGGGATGGTGTCAGGTAGGGATGCTC GAGTGGGGTGATGAACTTGACCACTGGTCAGGTGACTCTGGGGATGGTGTCAGGTAGGGATGCTC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:119915301..119915600 26863196 MeRIP-seq:(Medium) rs369912969 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 71306 RMVar_ID_71306 Human_SNP_ID_29867869 m1A Human chr1 + 119915672 119915672 119915672 TGCTGGGGCATCATGGCAGTGGGGAAAGCCACACTGGGCAAACGGGCCATTTCTGGAATCTGGTA TGCTGGGGCATCATGGCAGTGGGGAAAGCCACGCTGGGCAAACGGGCCATTTCTGGAATCTGGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119915621..119915803 26863196 MeRIP-seq:(Medium) rs1360707625 Functional Loss SNV dbSNP153 33..33 33 - - - 71307 RMVar_ID_71307 Human_SNP_ID_29868206 m1A Human chr1 + 119916540 119916540 119916540 GAGGGCTTGGGGTCACATTGTATTCATCCAGAAGGCGCACAATGTCATGGTGCATGCGATCCCGA GAGGGCTTGGGGTCACATTGTATTCATCCAGAGGGCGCACAATGTCATGGTGCATGCGATCCCGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:119916489..119916590 32194978 MeRIP-seq:(Medium) rs1553193616 Functional Loss SNV dbSNP153 33..33 33 - - - 71308 RMVar_ID_71308 Human_SNP_ID_29870040 m1A Human chr1 + 119923639 119923639 119923639 AGCCTTGAAGTTCAGAAACCAAACACCTACCCAGCCACCTCCTGTTCTTGTTCACCAGGAAGGGA AGCCTTGAAGTTCAGAAACCAAACACCTACCCTGCCACCTCCTGTTCTTGTTCACCAGGAAGGGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:119921738..119923669 32194978 MeRIP-seq:(Medium) rs778498447 Functional Loss SNV dbSNP153 33..33 33 - - - 71309 RMVar_ID_71309 Human_SNP_ID_29879430 m1A Human chr1 - 119963802 119963802 119963802 GAATCCTTGATAAAATTCTTTCCAAAGGTTTCACTGGTGTGTTGTGTGAGGAGAACATTGACAAC GAATCCTTGATAAAATTCTTTCCAAAGGTTTCGCTGGTGTGTTGTGTGAGGAGAACATTGACAAC T C NOTCH2 Ensembl:ENSG00000134250 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:119953562..119965537 32194978 MeRIP-seq:(Medium) rs1553199320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3987418,Human_RBP_ID_18549299,Human_RBP_ID_23327565 Human_Splice_Rec_115730,Human_Splice_Rec_115798,Human_Splice_Rec_115820,Human_Splice_Rec_115846 Human_miRNA_ID_2428041,Human_miRNA_ID_2449382,Human_miRNA_ID_2487840,Human_miRNA_ID_2538410 RMVar_hsa_circ_269815,RMVar_hsa_circ_107073,RMVar_hsa_circ_135747,RMVar_hsa_circ_64122,RMVar_hsa_circ_118779,RMVar_hsa_circ_115093,RMVar_hsa_circ_135753,RMVar_hsa_circ_135754,RMVar_hsa_circ_105732,RMVar_hsa_circ_266549,RMVar_hsa_circ_366158,RMVar_hsa_circ_135756,RMVar_hsa_circ_100067,RMVar_hsa_circ_74165,RMVar_hsa_circ_359380,RMVar_hsa_circ_115160,RMVar_hsa_circ_125415,RMVar_hsa_circ_135758,RMVar_hsa_circ_120928,RMVar_hsa_circ_111448,RMVar_hsa_circ_17139,RMVar_hsa_circ_37052,RMVar_hsa_circ_135760,RMVar_hsa_circ_135761,RMVar_hsa_circ_135762,RMVar_hsa_circ_135759 71310 RMVar_ID_71310 Human_SNP_ID_81907511 m1A Human chr2 - 90245270 90245270 90245270 AGACGGACAGCGGCGGAGAGGCAGACAGCGGCAGCGCGGCGGAGAGGCGGCCAGCGGCGGAGAGG AGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGCGCGGCGGAGAGGCGGCCAGCGGCGGAGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:90245103..90245421;chr2:90245101..90245440;chr2:90245089..90245422 26863196 MeRIP-seq:(Medium) rs1477945832 Functional Loss SNV dbSNP153 33..33 33 - - - 71311 RMVar_ID_71311 Human_SNP_ID_82044434 m1A Human chr2 + 91571458 91571458 91571458 GCGGACAGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGA GCGGACAGCGGCGGCGCGGCGGAGAGACGGACGGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:91571331..91571527;chr2:91571350..91571561;chr2:91571330..91571587;chr2:91571331..91571586 26863196 MeRIP-seq:(Medium) rs1210108509 Functional Loss SNV dbSNP153 33..33 33 - - - 71312 RMVar_ID_71312 Human_SNP_ID_82044446 m1A Human chr2 + 91571482 91571482 91571482 AGACGGACAGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGG AGACGGACAGCGGCGGCGCGGCGGCGCGGCGGCGAGACGGACAGCGGCGGAGAGGCAGACAGCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:91571323..91571608 26863196 MeRIP-seq:(Medium) rs1158514167 Functional Loss SNV dbSNP153 33..33 33 - - - 71313 RMVar_ID_71313 Human_SNP_ID_82044452 m1A Human chr2 + 91571490 91571490 91571490 AGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCAGCGCAG AGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGCCAGCGGCGGAGAGGCAGACAGCGGCAGCGCAG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:91571439..91571568 26863196 MeRIP-seq:(Medium) rs1194874507 Functional Loss SNV dbSNP153 33..33 33 - - - 71314 RMVar_ID_71314 Human_SNP_ID_82046487 m1A Human chr2 + 91577578 91577578 91577578 GTAGAGATGGGGTTTCGCCATGCTGCTCAGGCAGGTCTCAAACTCCTGGCCTCAAGCCATCTGCT GTAGAGATGGGGTTTCGCCATGCTGCTCAGGCGGGTCTCAAACTCCTGGCCTCAAGCCATCTGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:91577574..91577661 26863410 MeRIP-seq:(Medium) rs1191578305 Functional Loss SNV dbSNP153 33..33 33 - - - 71315 RMVar_ID_71315 Human_SNP_ID_82058026 m1A Human chr2 - 91623358 91623358 91623358 TCTCACTATGTTTGTGTTCCCTGGATGGTCTTAAACTCTTGGCCTCAAGCGATCCTTCTGTGTCA TCTCACTATGTTTGTGTTCCCTGGATGGTCTTCAACTCTTGGCCTCAAGCGATCCTTCTGTGTCA T G LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1292327297 Functional Loss SNV dbSNP153 33..33 33 - - - 71316 RMVar_ID_71316 Human_SNP_ID_82115541 m1A Human chr2 + 91809827 91809824 91809827 GCTTTTTGCTGGACCCGGCTTTTTGCCCCCCCACCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG GCTTTTTGCTGGACCCGGCTTTTTGCCCCC___CCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG CCCA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:91809819..91809942 26863196 MeRIP-seq:(Medium) rs1453727361 Functional Loss DEL dbSNP153 31..33 33 - - - 71317 RMVar_ID_71317 Human_SNP_ID_82115546 m1A Human chr2 + 91809827 91809827 91809827 GCTTTTTGCTGGACCCGGCTTTTTGCCCCCCCACCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG GCTTTTTGCTGGACCCGGCTTTTTGCCCCCCCCCCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:91809819..91809942 26863196 MeRIP-seq:(Medium) rs1407975382 Functional Loss SNV dbSNP153 33..33 33 - - - 71318 RMVar_ID_71318 Human_SNP_ID_82115547 m1A Human chr2 + 91809827 91809827 91809827 GCTTTTTGCTGGACCCGGCTTTTTGCCCCCCCACCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG GCTTTTTGCTGGACCCGGCTTTTTGCCCCCCCGCCGCCGCGGCTTCTTGCCCCCCGCCGCCGCGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:91809819..91809942 26863196 MeRIP-seq:(Medium) rs1407975382 Functional Loss SNV dbSNP153 33..33 33 - - - 71319 RMVar_ID_71319 Human_SNP_ID_83012797 m1A Human chr2 - 94208348 94208348 94208348 CGGAGAGGCGCACAGCGCAGGCGCTGGCGCGGAGAGGCGCAGGCCCAGGTCCACTCCCCAGCTGT CGGAGAGGCGCACAGCGCAGGCGCTGGCGCGGGGAGGCGCAGGCCCAGGTCCACTCCCCAGCTGT T C AC026273.1 Ensembl:ENSG00000286156 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:94208290..94208469 26863196 MeRIP-seq:(Medium) rs1490464307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_273045 71320 RMVar_ID_71320 Human_SNP_ID_83012922 m1A Human chr2 - 94208536 94208529 94208537 GCGGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCGGATAGCGGCG GCGGAGAGGCGGACAGCGGCGGCGCGGCGGA________CAGCGGCGGAGAGGCGGATAGCGGCG GTCCGCCTC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:94208451..94208744 26863410 MeRIP-seq:(Medium) rs1421065255 Functional Loss DEL dbSNP153 32..39 33 - - - 71321 RMVar_ID_71321 Human_SNP_ID_83012965 m1A Human chr2 + 94208634 94208634 94208634 CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGACCGACTCTCCGCTGCGCCGCCGCTATCCGCCT CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGCCCGACTCTCCGCTGCGCCGCCGCTATCCGCCT A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:94208487..94208714 26863410 MeRIP-seq:(Medium) rs1367863000 Functional Loss SNV dbSNP153 33..33 33 - - - 71322 RMVar_ID_71322 Human_SNP_ID_83012966 m1A Human chr2 + 94208634 94208634 94208634 CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGACCGACTCTCCGCTGCGCCGCCGCTATCCGCCT CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGGCCGACTCTCCGCTGCGCCGCCGCTATCCGCCT A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:94208487..94208714 26863410 MeRIP-seq:(Medium) rs1367863000 Functional Loss SNV dbSNP153 33..33 33 - - - 71323 RMVar_ID_71323 Human_SNP_ID_83012967 m1A Human chr2 + 94208634 94208634 94208634 CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGACCGACTCTCCGCTGCGCCGCCGCTATCCGCCT CCGCTGTCGGCCTCTCCGCCGCGCCGCCGCTGTCCGACTCTCCGCTGCGCCGCCGCTATCCGCCT A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:94208487..94208714 26863410 MeRIP-seq:(Medium) rs1367863000 Functional Loss SNV dbSNP153 33..33 33 - - - 71324 RMVar_ID_71324 Human_SNP_ID_83016838 m1A Human chr2 + 94219214 94219212 94219215 TGAAATGATGAGACGAAATGACAAAATTGAAAAGAAATTGAAAGGAGATGAGATGAGATAAAATG TGAAATGATGAGACGAAATGACAAAATTGAA___AAATTGAAAGGAGATGAGATGAGATAAAATG AAAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:94219172..94219318 26863196 MeRIP-seq:(Medium) rs1240973098 Functional Loss DEL dbSNP153 32..34 33 - - - 71325 RMVar_ID_71325 Human_SNP_ID_83016840 m1A Human chr2 + 94219216 94219216 94219216 AAATGATGAGACGAAATGACAAAATTGAAAAGAAATTGAAAGGAGATGAGATGAGATAAAATGAG AAATGATGAGACGAAATGACAAAATTGAAAAGGAATTGAAAGGAGATGAGATGAGATAAAATGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:94219161..94219335 26863196 MeRIP-seq:(Medium) rs1453776608 Functional Loss SNV dbSNP153 33..33 33 - - - 71326 RMVar_ID_71326 Human_SNP_ID_83016980 m1A Human chr2 - 94219528 94219528 94219528 ATGTCAAATCATCTCATTTCAATTTCATTTCAATTTCATCATTACATTTCATAATTTCCTTTCAT ATGTCAAATCATCTCATTTCAATTTCATTTCAGTTTCATCATTACATTTCATAATTTCCTTTCAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:94219394..94219619 26863196 MeRIP-seq:(Medium) rs1468229131 Functional Loss SNV dbSNP153 33..33 33 - - - 71327 RMVar_ID_71327 Human_SNP_ID_83016981 m1A Human chr2 - 94219528 94219528 94219528 ATGTCAAATCATCTCATTTCAATTTCATTTCAATTTCATCATTACATTTCATAATTTCCTTTCAT ATGTCAAATCATCTCATTTCAATTTCATTTCACTTTCATCATTACATTTCATAATTTCCTTTCAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:94219394..94219619 26863196 MeRIP-seq:(Medium) rs1468229131 Functional Loss SNV dbSNP153 33..33 33 - - - 71328 RMVar_ID_71328 Human_SNP_ID_83017018 m1A Human chr2 + 94219634 94219630 94219635 GATAAAATGAGATGAAATAATGAGATGAAATGAGATAATGAGATTGGATGAGATAAAATCATGAG GATAAAATGAGATGAAATAATGAGATGAA_____ATAATGAGATTGGATGAGATAAAATCATGAG AATGAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:94219584..94219654 26863196 MeRIP-seq:(Medium) rs1317432450 Functional Loss DEL dbSNP153 30..34 33 - - - 71329 RMVar_ID_71329 Human_SNP_ID_83017380 m1A Human chr2 - 94220398 94220395 94220399 CATCTCGTATCTTCTCATCTCATTTCGATTTCATTATTTCATTTATTTCATGTCATCTCATCTCA CATCTCGTATCTTCTCATCTCATTTCGATTT____ATTTCATTTATTTCATGTCATCTCATCTCA TAATG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:94220348..94220586 26863196 MeRIP-seq:(Medium) rs1424768397 Functional Loss DEL dbSNP153 32..35 33 - - - 71330 RMVar_ID_71330 Human_SNP_ID_83070657 m1A Human chr2 - 94586658 94586658 94586658 GGCCTGGCCCTCCAAGGGCCCCTAGTCTGAGGAGCAGTCCACCTGCCCTCGGGAAAACACCTCCC GGCCTGGCCCTCCAAGGGCCCCTAGTCTGAGGTGCAGTCCACCTGCCCTCGGGAAAACACCTCCC T A AL845331.3 Ensembl:ENSG00000261522 Pseudogene intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:94586611..94586695 26863410 MeRIP-seq:(Medium) rs1455623350 Functional Loss SNV dbSNP153 33..33 33 - - - 71331 RMVar_ID_71331 Human_SNP_ID_83070658 m1A Human chr2 - 94586658 94586658 94586658 GGCCTGGCCCTCCAAGGGCCCCTAGTCTGAGGAGCAGTCCACCTGCCCTCGGGAAAACACCTCCC GGCCTGGCCCTCCAAGGGCCCCTAGTCTGAGGCGCAGTCCACCTGCCCTCGGGAAAACACCTCCC T G AL845331.3 Ensembl:ENSG00000261522 Pseudogene intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:94586611..94586695 26863410 MeRIP-seq:(Medium) rs1455623350 Functional Loss SNV dbSNP153 33..33 33 - - - 71332 RMVar_ID_71332 Human_SNP_ID_83216592 m1A Human chr2 + 95091357 95091357 95091357 TTCAAGGTCCCACTCAAATTGCTCCTCTTCAGACAGGCCTTCTGTGACCATGCTATTCAAGGTGG TTCAAGGTCCCACTCAAATTGCTCCTCTTCAGCCAGGCCTTCTGTGACCATGCTATTCAAGGTGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:95091354..95091454 26863196 MeRIP-seq:(Medium) rs1558675529 Functional Loss SNV dbSNP153 33..33 33 - - - 71333 RMVar_ID_71333 Human_SNP_ID_83220086 m1A Human chr2 - 95106453 95106453 95106453 TGTATCCCTGTTTCTTTTCTCCCTACAGAAACATATGAGGATTTTGATACCAGGATACTTGAGGT TGTATCCCTGTTTCTTTTCTCCCTACAGAAACGTATGAGGATTTTGATACCAGGATACTTGAGGT T C MRPS5 Ensembl:ENSG00000144029 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:95106451..95106475 26863196 MeRIP-seq:(Medium) rs747347250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915636,Human_RBP_ID_1067669,Human_RBP_ID_8234410,Human_RBP_ID_9384217,Human_RBP_ID_18999854,Human_RBP_ID_19100991,Human_RBP_ID_21982266,Human_RBP_ID_26338624,Human_RBP_ID_27817315 Human_Splice_Rec_273236,Human_Splice_Rec_273237,Human_Splice_Rec_273260,Human_Splice_Rec_273261,Human_Splice_Rec_273279,Human_Splice_Rec_273298,Human_Splice_Rec_273299,Human_Splice_Rec_273301 RMVar_hsa_circ_27338,RMVar_hsa_circ_88336,RMVar_hsa_circ_119653,RMVar_hsa_circ_201780,RMVar_hsa_circ_201781,RMVar_hsa_circ_341041 71334 RMVar_ID_71334 Human_SNP_ID_83220473 m1A Human chr2 + 95108194 95108193 95108194 AGGAGTTTGCTACCTCCACAGGGACCAGGGTCAGGGGGGCCAAGACTGATGCCTCCCCATGAGTT AGGAGTTTGCTACCTCCACAGGGACCAGGGTC_GGGGGGCCAAGACTGATGCCTCCCCATGAGTT CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:95108176..95108425 32194978 MeRIP-seq:(Medium) rs1218332257 Functional Loss DEL dbSNP153 33..33 33 - - - 71335 RMVar_ID_71335 Human_SNP_ID_83222844 m1A Human chr2 + 95117944 95117944 95117944 GTGTTTAGGGAACACTGCCTCCCCAATAAATGACCTGCAAATTGGAAAAAAAAAAATTTAAGATA GTGTTTAGGGAACACTGCCTCCCCAATAAATGGCCTGCAAATTGGAAAAAAAAAAATTTAAGATA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:95117901..95121953 26863196 MeRIP-seq:(Medium) rs1241448245 Functional Loss SNV dbSNP153 33..33 33 - - - 71336 RMVar_ID_71336 Human_SNP_ID_83222845 m1A Human chr2 + 95117944 95117944 95117944 GTGTTTAGGGAACACTGCCTCCCCAATAAATGACCTGCAAATTGGAAAAAAAAAAATTTAAGATA GTGTTTAGGGAACACTGCCTCCCCAATAAATGTCCTGCAAATTGGAAAAAAAAAAATTTAAGATA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:95117901..95121953 26863196 MeRIP-seq:(Medium) rs1241448245 Functional Loss SNV dbSNP153 33..33 33 - - - 71337 RMVar_ID_71337 Human_SNP_ID_83223705 m1A Human chr2 + 95121702 95121702 95121702 CCCCAGGCGAGCCCCCCACTCCCGGCCCGCTCAGAGCCCCTGCTCCCGGCGTCCCAGCTCTCACC CCCCAGGCGAGCCCCCCACTCCCGGCCCGCTCTGAGCCCCTGCTCCCGGCGTCCCAGCTCTCACC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:95121699..95121872 26863196 MeRIP-seq:(Medium) rs1275760876 Functional Loss SNV dbSNP153 33..33 33 - - - 71338 RMVar_ID_71338 Human_SNP_ID_83223732 m1A Human chr2 + 95121754 95121754 95121754 CCCAGCTCTCACCTGCCGTCCCGCTACACAGCACGGGGAGGCAGCCCACAGCGCGCACCGCGGTC CCCAGCTCTCACCTGCCGTCCCGCTACACAGCCCGGGGAGGCAGCCCACAGCGCGCACCGCGGTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:95117915..95121934 26863196 MeRIP-seq:(Medium) rs776345512 Functional Loss SNV dbSNP153 33..33 33 - - - 71339 RMVar_ID_71339 Human_SNP_ID_83223805 m1A Human chr2 - 95121835 95121835 95121835 TTGACGAGGAGCAGTCGCGGTAGGCGGTGGGCAAGGCTGCCCTGGGCGGAGGCCGAGGCGCGGCT TTGACGAGGAGCAGTCGCGGTAGGCGGTGGGCGAGGCTGCCCTGGGCGGAGGCCGAGGCGCGGCT T C MRPS5 Ensembl:ENSG00000144029 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:95121726..95121944 26863196 MeRIP-seq:(Medium) rs774202132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4620058,Human_RBP_ID_8851392,Human_RBP_ID_9296666,Human_RBP_ID_17963088,Human_RBP_ID_18470818,Human_RBP_ID_22451492,Human_RBP_ID_27818696 71340 RMVar_ID_71340 Human_SNP_ID_83223818 m1A Human chr2 + 95121887 95121887 95121887 TGCTCCTCGTCAAACGGCAAGCCTTGGGCCGCAGCGGAATTCCTGAGGCCCGAGTCCACGCAGCA TGCTCCTCGTCAAACGGCAAGCCTTGGGCCGCGGCGGAATTCCTGAGGCCCGAGTCCACGCAGCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:95121785..95121949 26863410 MeRIP-seq:(Medium) rs1452873376 Functional Loss SNV dbSNP153 33..33 33 - - - 71341 RMVar_ID_71341 Human_SNP_ID_83232066 m1A Human chr2 - 95159399 95159399 95159399 ATAGAGTCGGTCCCTGCTCCTGTGAGGCTCTCACCGAATCCCTGCTGTTTCCGGGCAGCTGAAGA ATAGAGTCGGTCCCTGCTCCTGTGAGGCTCTCGCCGAATCCCTGCTGTTTCCGGGCAGCTGAAGA T C ZNF514 Ensembl:ENSG00000144026 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:95159008..95159542 26863196 MeRIP-seq:(Medium) rs978019612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1379355,Human_RBP_ID_3640873,Human_RBP_ID_9428748,Human_RBP_ID_21981172,Human_RBP_ID_22547416,Human_RBP_ID_22667510 71342 RMVar_ID_71342 Human_SNP_ID_83237233 m1A Human chr2 + 95181318 95181318 95181318 ACAAAGGCTTGCGGCGACGGTCAGCCCTGTCCAGGGAAATTCTCACTAAAGAGAGACACCAGGAA ACAAAGGCTTGCGGCGACGGTCAGCCCTGTCCGGGGAAATTCTCACTAAAGAGAGACACCAGGAA A G ZNF2 Ensembl:ENSG00000275111 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:95181270..95181421 32194978 MeRIP-seq:(Medium) rs1399082750 Functional Loss SNV dbSNP153 33..33 33 - - - 71343 RMVar_ID_71343 Human_SNP_ID_83237234 m1A Human chr2 + 95181318 95181318 95181318 ACAAAGGCTTGCGGCGACGGTCAGCCCTGTCCAGGGAAATTCTCACTAAAGAGAGACACCAGGAA ACAAAGGCTTGCGGCGACGGTCAGCCCTGTCCTGGGAAATTCTCACTAAAGAGAGACACCAGGAA A T ZNF2 Ensembl:ENSG00000275111 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:95181270..95181421 32194978 MeRIP-seq:(Medium) rs1399082750 Functional Loss SNV dbSNP153 33..33 33 - - - 71344 RMVar_ID_71344 Human_SNP_ID_83358447 m1A Human chr2 + 95814653 95814653 95814653 TCCATCTTGAAATGTCCTCTCCCTCAGTTCCTATATGTTATCACACATGCCTGCCTTGGCTTCTC TCCATCTTGAAATGTCCTCTCCCTCAGTTCCTTTATGTTATCACACATGCCTGCCTTGGCTTCTC A T lnc-TRIM43-9 RNACentral:URS00008B528D lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:95814602..95814719 26863196 MeRIP-seq:(Medium) rs1392434355 Functional Loss SNV dbSNP153 33..33 33 - - - 71345 RMVar_ID_71345 Human_SNP_ID_83362214 m1A Human chr2 - 95831975 95831975 95831975 CCAGTCACTCCTGCTGGTGTTCTCGGGCCCAAAGATATTTGAATTCTTGGGATGAGATGGCCAAA CCAGTCACTCCTGCTGGTGTTCTCGGGCCCAACGATATTTGAATTCTTGGGATGAGATGGCCAAA T G LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:95831926..95832038 32194978 MeRIP-seq:(Medium) rs1231197521 Functional Loss SNV dbSNP153 33..33 33 - - - 71346 RMVar_ID_71346 Human_SNP_ID_83437420 m1A Human chr2 + 96143464 96143464 96143464 AGACGAACCCACAGACAGGGCTCCTGGTTGTCACAGCTTGTTCCTTGGAGCTCTCAGGCTGCCAA AGACGAACCCACAGACAGGGCTCCTGGTTGTCCCAGCTTGTTCCTTGGAGCTCTCAGGCTGCCAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96143413..96143661 32194978 MeRIP-seq:(Medium) rs1363052805 Functional Loss SNV dbSNP153 33..33 33 - - - 71347 RMVar_ID_71347 Human_SNP_ID_83437548 m1A Human chr2 - 96143926 96143926 96143926 ATACCTCATGCAGAGTCGCCGTGTGCGGCTGGACGAGGCCTTTGACTTCGTTAAGCAGCGCCGGG ATACCTCATGCAGAGTCGCCGTGTGCGGCTGGGCGAGGCCTTTGACTTCGTTAAGCAGCGCCGGG T C DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:96143876..96143950 26863196 MeRIP-seq:(Medium) rs1253353645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94669,RMVar_hsa_circ_201829 71348 RMVar_ID_71348 Human_SNP_ID_83437713 m1A Human chr2 - 96144273 96144273 96144273 GCTGCAGGCCTGTGGCATCACAGCCGTCCTCAACGTGTCCGCCAGCTGCCCCAACCACTTTGAGG GCTGCAGGCCTGTGGCATCACAGCCGTCCTCAGCGTGTCCGCCAGCTGCCCCAACCACTTTGAGG T C DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96144222..96144371 32194978 MeRIP-seq:(Medium) rs1444745129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1961400 RMVar_hsa_circ_94669,RMVar_hsa_circ_201829 71349 RMVar_ID_71349 Human_SNP_ID_83437927 m1A Human chr2 - 96144799 96144799 96144799 CCGCCCCTGCGCTGCCGCCAACAGGGGACAAAACCAGCCGCTCCGACTCCAGGGCTCCTGTCTAC CCGCCCCTGCGCTGCCGCCAACAGGGGACAAATCCAGCCGCTCCGACTCCAGGGCTCCTGTCTAC T A DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:96144776..96144800 26863196 MeRIP-seq:(Medium) rs201093774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_274708,Human_Splice_Rec_274709 RMVar_hsa_circ_32470 71350 RMVar_ID_71350 Human_SNP_ID_83437928 m1A Human chr2 - 96144799 96144799 96144799 CCGCCCCTGCGCTGCCGCCAACAGGGGACAAAACCAGCCGCTCCGACTCCAGGGCTCCTGTCTAC CCGCCCCTGCGCTGCCGCCAACAGGGGACAAACCCAGCCGCTCCGACTCCAGGGCTCCTGTCTAC T G DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:96144776..96144800 26863196 MeRIP-seq:(Medium) rs201093774 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_274708,Human_Splice_Rec_274709 RMVar_hsa_circ_32470 71351 RMVar_ID_71351 Human_SNP_ID_83437973 m1A Human chr2 + 96144877 96144877 96144877 CAGATCGGGACAGCAGCCCTGGAAGCCGTCGAAGCCTCCTGCAAGGAGGGGAAGAGCACGATCAG CAGATCGGGACAGCAGCCCTGGAAGCCGTCGAGGCCTCCTGCAAGGAGGGGAAGAGCACGATCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96144828..96145039 26863196 MeRIP-seq:(Medium) rs754112547 Functional Loss SNV dbSNP153 33..33 33 - - - 71352 RMVar_ID_71352 Human_SNP_ID_83437974 m1A Human chr2 + 96144877 96144877 96144877 CAGATCGGGACAGCAGCCCTGGAAGCCGTCGAAGCCTCCTGCAAGGAGGGGAAGAGCACGATCAG CAGATCGGGACAGCAGCCCTGGAAGCCGTCGATGCCTCCTGCAAGGAGGGGAAGAGCACGATCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96144828..96145039 26863196 MeRIP-seq:(Medium) rs754112547 Functional Loss SNV dbSNP153 33..33 33 - - - 71353 RMVar_ID_71353 Human_SNP_ID_83437980 m1A Human chr2 - 96144884 96144884 96144884 TTCCCTGCTGATCGTGCTCTTCCCCTCCTTGCAGGAGGCTTCGACGGCTTCCAGGGCTGCTGTCC TTCCCTGCTGATCGTGCTCTTCCCCTCCTTGCGGGAGGCTTCGACGGCTTCCAGGGCTGCTGTCC T C DUSP2 Ensembl:ENSG00000158050 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96144860..96145242 32194978 MeRIP-seq:(Medium) rs1362151662 Functional Loss SNV dbSNP153 33..33 33 - - - 71354 RMVar_ID_71354 Human_SNP_ID_83438016 m1A Human chr2 + 96144947 96144947 96144947 AAAGCCGGGCTGGAGTCGGGTGGGGCGGGCCAAGGGCGGCCGGCTTGCTCACCTCGCAGGAAGTA AAAGCCGGGCTGGAGTCGGGTGGGGCGGGCCAGGGGCGGCCGGCTTGCTCACCTCGCAGGAAGTA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96144901..96144950 26863196 MeRIP-seq:(Medium) rs1300484982 Functional Loss SNV dbSNP153 33..33 33 - - - 71355 RMVar_ID_71355 Human_SNP_ID_83438075 m1A Human chr2 + 96145026 96145026 96145026 CCGCGCGGGTCTCGTGCAGCAGCGCGGCCAGCAGCACATGAGCCGGGCTGTCGGGCCGGAGCTCC CCGCGCGGGTCTCGTGCAGCAGCGCGGCCAGCGGCACATGAGCCGGGCTGTCGGGCCGGAGCTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr2:96145001..96145025;chr2:96144976..96145050;chr2:96144892..96145150 26863196 MeRIP-seq:(Medium) rs1355569559 Functional Loss SNV dbSNP153 33..33 33 - - - 71356 RMVar_ID_71356 Human_SNP_ID_83453915 m1A Human chr2 + 96208376 96208376 96208376 TGACGAAGCGGCACTGATTGGCCAGAAGCGCCAGCAGGCCCCCGCCCCGCGTCCCCGCCAGCCAG TGACGAAGCGGCACTGATTGGCCAGAAGCGCCGGCAGGCCCCCGCCCCGCGTCCCCGCCAGCCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:96208327..96208538 26863196 MeRIP-seq:(Medium) rs748351378 Functional Loss SNV dbSNP153 33..33 33 - - - 71357 RMVar_ID_71357 Human_SNP_ID_83454082 m1A Human chr2 - 96208715 96208715 96208715 TCCCGGCCCCGGGCGCCCGCTGGAGGTCGCCGAGGAGCCACAGGGCTGACTGGTCTGCTGCCCGG TCCCGGCCCCGGGCGCCCGCTGGAGGTCGCCGGGGAGCCACAGGGCTGACTGGTCTGCTGCCCGG T C STARD7 Ensembl:ENSG00000084090 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:96208615..96208825 26863410 MeRIP-seq:(Medium) rs1277471877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777918,Human_RBP_ID_4622544,Human_RBP_ID_5322523,Human_RBP_ID_5471426,Human_RBP_ID_5527877,Human_RBP_ID_8851395,Human_RBP_ID_9296669,Human_RBP_ID_9330558,Human_RBP_ID_22076456,Human_RBP_ID_22451497 71358 RMVar_ID_71358 Human_SNP_ID_83454101 m1A Human chr2 + 96208773 96208770 96208774 GCCGGGATGCAGGGCGCGCGGACAGAAACGAGACAGACAGCTCAGGCCCAGCAGCACGCAAGCTC GCCGGGATGCAGGGCGCGCGGACAGAAACG____AGACAGCTCAGGCCCAGCAGCACGCAAGCTC GAGAC G STARD7-AS1 Ensembl:ENSG00000204685 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96208336..96208825 26863196 MeRIP-seq:(Medium) rs1558739491 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5594447 71359 RMVar_ID_71359 Human_SNP_ID_83454102 m1A Human chr2 + 96208773 96208773 96208773 GCCGGGATGCAGGGCGCGCGGACAGAAACGAGACAGACAGCTCAGGCCCAGCAGCACGCAAGCTC GCCGGGATGCAGGGCGCGCGGACAGAAACGAGGCAGACAGCTCAGGCCCAGCAGCACGCAAGCTC A G STARD7-AS1 Ensembl:ENSG00000204685 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96208336..96208825 26863196 MeRIP-seq:(Medium) rs558656865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5594447 71360 RMVar_ID_71360 Human_SNP_ID_83464730 m1A Human chr2 - 96253675 96253675 96253675 ATCCTGACCATCTTCTCCAAACCTTCCCCAGGAGAGACTCTGCCTTTAGGGTCATCCAAGTATCC ATCCTGACCATCTTCTCCAAACCTTCCCCAGGTGAGACTCTGCCTTTAGGGTCATCCAAGTATCC T A TMEM127 Ensembl:ENSG00000135956 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:96253624..96253775 26863196 MeRIP-seq:(Medium) rs890856077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557979,Human_RBP_ID_1024603,Human_RBP_ID_6958568,Human_RBP_ID_17278469,Human_RBP_ID_18767456,Human_RBP_ID_27482592 71361 RMVar_ID_71361 Human_SNP_ID_83467477 m1A Human chr2 - 96265188 96265188 96265188 GCACATCCACGGAGGCACCTGTTCGCGCCAGGAGCTGGGGGTCTCCGACGTGTTGGGCTATGTGC GCACATCCACGGAGGCACCTGTTCGCGCCAGGGGCTGGGGGTCTCCGACGTGTTGGGCTATGTGC T C TMEM127 Ensembl:ENSG00000135956 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96260548..96265190 32194978 MeRIP-seq:(Medium) rs1239429978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1024604 Human_Splice_Rec_274779,Human_Splice_Rec_274785 71362 RMVar_ID_71362 Human_SNP_ID_83467579 m1A Human chr2 - 96265381 96265381 96265381 CGACTGCGGAGCGACGGCGGGCGGCCCCGGGCATGTACGCCCCCGGAGGCGCAGGGCTGCCCGGC CGACTGCGGAGCGACGGCGGGCGGCCCCGGGCGTGTACGCCCCCGGAGGCGCAGGGCTGCCCGGC T C TMEM127 Ensembl:ENSG00000135956 Protein coding start codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96265339..96265944 32194978 MeRIP-seq:(Medium) rs1553437759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776962,Human_RBP_ID_1067945,Human_RBP_ID_4622549,Human_RBP_ID_22450472 71363 RMVar_ID_71363 Human_SNP_ID_83467921 m1A Human chr2 + 96266328 96266328 96266328 CGCTGTCTGCTCAGCGGACTCTGCCCGCCCCCACCTCCCCCTGCGTCGGGCCGACATGAAGGACT CGCTGTCTGCTCAGCGGACTCTGCCCGCCCCCCCCTCCCCCTGCGTCGGGCCGACATGAAGGACT A C CIAO1 Ensembl:ENSG00000144021 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96266277..96266422 26863196 MeRIP-seq:(Medium) rs754904404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557984,Human_RBP_ID_4620523,Human_RBP_ID_5322524,Human_RBP_ID_5471168,Human_RBP_ID_8257735,Human_RBP_ID_8850648,Human_RBP_ID_9296671,Human_RBP_ID_22450474 71364 RMVar_ID_71364 Human_SNP_ID_83467922 m1A Human chr2 + 96266328 96266328 96266328 CGCTGTCTGCTCAGCGGACTCTGCCCGCCCCCACCTCCCCCTGCGTCGGGCCGACATGAAGGACT CGCTGTCTGCTCAGCGGACTCTGCCCGCCCCCGCCTCCCCCTGCGTCGGGCCGACATGAAGGACT A G CIAO1 Ensembl:ENSG00000144021 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96266277..96266422 26863196 MeRIP-seq:(Medium) rs754904404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557984,Human_RBP_ID_4620523,Human_RBP_ID_5322524,Human_RBP_ID_5471168,Human_RBP_ID_8257735,Human_RBP_ID_8850648,Human_RBP_ID_9296671,Human_RBP_ID_22450474 71365 RMVar_ID_71365 Human_SNP_ID_83468755 m1A Human chr2 - 96269020 96269020 96269020 GTATGTAACTACTTTGCGTGCCTGTGAAGGCCACCCACCAGCCGACCCAACCCACTTTATTCCTC GTATGTAACTACTTTGCGTGCCTGTGAAGGCCGCCCACCAGCCGACCCAACCCACTTTATTCCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:96268867..96269143 26863196 MeRIP-seq:(Medium) rs762672313 Functional Loss SNV dbSNP153 33..33 33 - - - 71366 RMVar_ID_71366 Human_SNP_ID_83469492 m1A Human chr2 + 96271401 96271401 96271401 CAGAGTAATGACTCCCCAGAAAACGTCATATAAGACTTTACCAGCCCCTGAGAGGACCAGGAGGA CAGAGTAATGACTCCCCAGAAAACGTCATATAGGACTTTACCAGCCCCTGAGAGGACCAGGAGGA A G CIAO1 Ensembl:ENSG00000144021 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96271351..96271425 26863196 MeRIP-seq:(Medium) rs768947487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1591680,Human_RBP_ID_1925099,Human_RBP_ID_8850666,Human_RBP_ID_9384242,Human_RBP_ID_18319967,Human_RBP_ID_23211655,Human_RBP_ID_26339558,Human_RBP_ID_27016442,Human_RBP_ID_27293560,Human_RBP_ID_27482614 71367 RMVar_ID_71367 Human_SNP_ID_83470432 m1A Human chr2 - 96274802 96274802 96274802 AGCAGGTGTCATGGGTCAAGCATAAATCATATATAGCATTTTCAGGCATGTTCCTGGTAGTTCTT AGCAGGTGTCATGGGTCAAGCATAAATCATATGTAGCATTTTCAGGCATGTTCCTGGTAGTTCTT T C SNRNP200 Ensembl:ENSG00000144028 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96274751..96275000 32194978 MeRIP-seq:(Medium) rs947792135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_306420,Human_RBP_ID_558062,Human_RBP_ID_1925119,Human_RBP_ID_2668679,Human_RBP_ID_5502744,Human_RBP_ID_6958645,Human_RBP_ID_8850713,Human_RBP_ID_9113295,Human_RBP_ID_17278470,Human_RBP_ID_17392440,Human_RBP_ID_17658556,Human_RBP_ID_17963301,Human_RBP_ID_18319995,Human_RBP_ID_22999372,Human_RBP_ID_24424024,Human_RBP_ID_24490569,Human_RBP_ID_27699457 71368 RMVar_ID_71368 Human_SNP_ID_83471026 m1A Human chr2 + 96276974 96276974 96276974 CCTCCTCTCGCTCCAGCTGCACCAGCACCACAACTGGCCCGCCACTGCAGGGGGAGAGGAGGGGC CCTCCTCTCGCTCCAGCTGCACCAGCACCACAGCTGGCCCGCCACTGCAGGGGGAGAGGAGGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96276926..96277166 26863196 MeRIP-seq:(Medium) rs1348016504 Functional Loss SNV dbSNP153 33..33 33 - - - 71369 RMVar_ID_71369 Human_SNP_ID_83471027 m1A Human chr2 - 96276976 96276976 96276976 GCGCCCCTCCTCTCCCCCTGCAGTGGCGGGCCAGTTGTGGTGCTGGTGCAGCTGGAGCGAGAGGA GCGCCCCTCCTCTCCCCCTGCAGTGGCGGGCCGGTTGTGGTGCTGGTGCAGCTGGAGCGAGAGGA T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr2:96276901..96277199;chr2:96276901..96277200;chr2:96276926..96277097;chr2:96276926..96277000 26863196,32194978 MeRIP-seq:(Medium) rs1400156636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242915,Human_RBP_ID_22449913 Human_Splice_Rec_274904,Human_Splice_Rec_274905,Human_Splice_Rec_274932,Human_Splice_Rec_274933,Human_Splice_Rec_274962,Human_Splice_Rec_274963 Human_miRNA_ID_2155016,Human_miRNA_ID_2158577,Human_miRNA_ID_2299249,Human_miRNA_ID_2302520,Human_miRNA_ID_2305784 RMVar_hsa_circ_28103,RMVar_hsa_circ_79633,RMVar_hsa_circ_115350,RMVar_hsa_circ_88869,RMVar_hsa_circ_88486,RMVar_hsa_circ_109508,RMVar_hsa_circ_126136,RMVar_hsa_circ_201840,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_201841,RMVar_hsa_circ_373294,RMVar_hsa_circ_291544,RMVar_hsa_circ_125348,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_83181,RMVar_hsa_circ_201844,RMVar_hsa_circ_201846,RMVar_hsa_circ_201848,RMVar_hsa_circ_201849,RMVar_hsa_circ_201850,RMVar_hsa_circ_201847,RMVar_hsa_circ_201845 71370 RMVar_ID_71370 Human_SNP_ID_83471332 m1A Human chr2 - 96277907 96277907 96277907 GGTCCCCCACAAGCTGAATAACCCTAAGTTCAATGATCCGCACGTCAAGACCAACCTGCTCCTGC GGTCCCCCACAAGCTGAATAACCCTAAGTTCAGTGATCCGCACGTCAAGACCAACCTGCTCCTGC T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96277856..96277967 26863196 MeRIP-seq:(Medium) rs1295558388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1925131,Human_RBP_ID_9260025,Human_RBP_ID_17392988,Human_RBP_ID_18544587 Human_Splice_Rec_274898,Human_Splice_Rec_274926,Human_Splice_Rec_274956,Human_Splice_Rec_274968 RMVar_hsa_circ_79633,RMVar_hsa_circ_115350,RMVar_hsa_circ_88869,RMVar_hsa_circ_88486,RMVar_hsa_circ_109508,RMVar_hsa_circ_126136,RMVar_hsa_circ_201840,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_201841,RMVar_hsa_circ_125348,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_83181,RMVar_hsa_circ_201844,RMVar_hsa_circ_201846,RMVar_hsa_circ_201848,RMVar_hsa_circ_201849,RMVar_hsa_circ_201847,RMVar_hsa_circ_201845,RMVar_hsa_circ_201851,RMVar_hsa_circ_106112 71371 RMVar_ID_71371 Human_SNP_ID_83472814 m1A Human chr2 - 96283704 96283704 96283704 CTTTTCTTCTCCCCGGTCGCCAGGGCTTCAACATCAGCCATACACAAACCCGCCTGCTCTCCATG CTTTTCTTCTCCCCGGTCGCCAGGGCTTCAACTTCAGCCATACACAAACCCGCCTGCTCTCCATG T A SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96283701..96283725 26863196 MeRIP-seq:(Medium) rs771740670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923224,Human_RBP_ID_18193345,Human_RBP_ID_18767517 Human_Splice_Rec_274884,Human_Splice_Rec_274912,Human_Splice_Rec_274942,Human_Splice_Rec_274976 Human_miRNA_ID_2976182 RMVar_hsa_circ_79633,RMVar_hsa_circ_115350,RMVar_hsa_circ_88869,RMVar_hsa_circ_109508,RMVar_hsa_circ_126136,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_201841,RMVar_hsa_circ_125348,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_84227,RMVar_hsa_circ_94313,RMVar_hsa_circ_201844,RMVar_hsa_circ_201846,RMVar_hsa_circ_201848,RMVar_hsa_circ_201847,RMVar_hsa_circ_201845,RMVar_hsa_circ_126625,RMVar_hsa_circ_201851,RMVar_hsa_circ_106112,RMVar_hsa_circ_201853,RMVar_hsa_circ_86517,RMVar_hsa_circ_92441,RMVar_hsa_circ_201854,RMVar_hsa_circ_201855,RMVar_hsa_circ_112457,RMVar_hsa_circ_201857,RMVar_hsa_circ_53549,RMVar_hsa_circ_201858,RMVar_hsa_circ_201859,RMVar_hsa_circ_122198,RMVar_hsa_circ_371474,RMVar_hsa_circ_46751,RMVar_hsa_circ_92923,RMVar_hsa_circ_201862,RMVar_hsa_circ_201863,RMVar_hsa_circ_201861 71372 RMVar_ID_71372 Human_SNP_ID_83472815 m1A Human chr2 - 96283704 96283704 96283704 CTTTTCTTCTCCCCGGTCGCCAGGGCTTCAACATCAGCCATACACAAACCCGCCTGCTCTCCATG CTTTTCTTCTCCCCGGTCGCCAGGGCTTCAACGTCAGCCATACACAAACCCGCCTGCTCTCCATG T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96283701..96283725 26863196 MeRIP-seq:(Medium) rs771740670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923224,Human_RBP_ID_18193345,Human_RBP_ID_18767517 Human_Splice_Rec_274884,Human_Splice_Rec_274912,Human_Splice_Rec_274942,Human_Splice_Rec_274976 Human_miRNA_ID_2976182 RMVar_hsa_circ_79633,RMVar_hsa_circ_115350,RMVar_hsa_circ_88869,RMVar_hsa_circ_109508,RMVar_hsa_circ_126136,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_201841,RMVar_hsa_circ_125348,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_84227,RMVar_hsa_circ_94313,RMVar_hsa_circ_201844,RMVar_hsa_circ_201846,RMVar_hsa_circ_201848,RMVar_hsa_circ_201847,RMVar_hsa_circ_201845,RMVar_hsa_circ_126625,RMVar_hsa_circ_201851,RMVar_hsa_circ_106112,RMVar_hsa_circ_201853,RMVar_hsa_circ_86517,RMVar_hsa_circ_92441,RMVar_hsa_circ_201854,RMVar_hsa_circ_201855,RMVar_hsa_circ_112457,RMVar_hsa_circ_201857,RMVar_hsa_circ_53549,RMVar_hsa_circ_201858,RMVar_hsa_circ_201859,RMVar_hsa_circ_122198,RMVar_hsa_circ_371474,RMVar_hsa_circ_46751,RMVar_hsa_circ_92923,RMVar_hsa_circ_201862,RMVar_hsa_circ_201863,RMVar_hsa_circ_201861 71373 RMVar_ID_71373 Human_SNP_ID_83472921 m1A Human chr2 + 96284002 96284002 96284002 TAGCGCATTCGGGAGCAGATCACTTCTAAGACAGGCTGGAAAGAGGGAGGGAGGGAGGGTCACTG TAGCGCATTCGGGAGCAGATCACTTCTAAGACGGGCTGGAAAGAGGGAGGGAGGGAGGGTCACTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:96283951..96284025 32194978 MeRIP-seq:(Medium) rs768996132 Functional Loss SNV dbSNP153 33..33 33 - - - 71374 RMVar_ID_71374 Human_SNP_ID_83476247 m1A Human chr2 - 96296982 96296982 96296982 CAAAACACTGAATCGGATCCAGAGTAAGCTCTACCGTGCTGCCCTTGAGACGGATGAGAATCTGC CAAAACACTGAATCGGATCCAGAGTAAGCTCTGCCGTGCTGCCCTTGAGACGGATGAGAATCTGC T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96296905..96297009 26863196 MeRIP-seq:(Medium) rs1259944697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_305707,Human_RBP_ID_4635469,Human_RBP_ID_5195319,Human_RBP_ID_5589687,Human_RBP_ID_8527333,Human_RBP_ID_8850820 Human_Splice_Rec_274842,Human_Splice_Rec_274843,Human_Splice_Rec_275022,Human_Splice_Rec_275023 Human_miRNA_ID_2780625,Human_miRNA_ID_2786193 RMVar_hsa_circ_79633,RMVar_hsa_circ_88869,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_201844,RMVar_hsa_circ_201845,RMVar_hsa_circ_84091,RMVar_hsa_circ_201865,RMVar_hsa_circ_98292,RMVar_hsa_circ_78669,RMVar_hsa_circ_46281,RMVar_hsa_circ_201866,RMVar_hsa_circ_77402,RMVar_hsa_circ_201867,RMVar_hsa_circ_115047,RMVar_hsa_circ_75633,RMVar_hsa_circ_201869,RMVar_hsa_circ_201870,RMVar_hsa_circ_92734,RMVar_hsa_circ_201874,RMVar_hsa_circ_201873,RMVar_hsa_circ_43933 71375 RMVar_ID_71375 Human_SNP_ID_83476919 m1A Human chr2 - 96299414 96299414 96299414 GTTGGGGTCATTTCCACAGGAAGGTGATGAAGACGTATACGGGGAGGTTCGAGAAGAGGCATCTG GTTGGGGTCATTTCCACAGGAAGGTGATGAAGGCGTATACGGGGAGGTTCGAGAAGAGGCATCTG T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr2:96299296..96299476;chr2:96299295..96299493 26863196 MeRIP-seq:(Medium) rs770981197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59326,Human_RBP_ID_776057,Human_RBP_ID_923337,Human_RBP_ID_2668702,Human_RBP_ID_3958070,Human_RBP_ID_8852064,Human_RBP_ID_9259872,Human_RBP_ID_9296754,Human_RBP_ID_9384277,Human_RBP_ID_22452391,Human_RBP_ID_26339569 Human_Splice_Rec_274830,Human_Splice_Rec_274831,Human_Splice_Rec_275010,Human_Splice_Rec_275011 RMVar_hsa_circ_88869,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_201844,RMVar_hsa_circ_201845,RMVar_hsa_circ_78669,RMVar_hsa_circ_201866,RMVar_hsa_circ_77402,RMVar_hsa_circ_201867,RMVar_hsa_circ_92734,RMVar_hsa_circ_201874,RMVar_hsa_circ_59344,RMVar_hsa_circ_43933,RMVar_hsa_circ_67902 71376 RMVar_ID_71376 Human_SNP_ID_83477317 m1A Human chr2 - 96300999 96300999 96300999 CGGTGTGAATGTGCAGTTTGAGTCTGATGAGGAGGTGAGTGATAAACATACCCAGTCCATTCTTG CGGTGTGAATGTGCAGTTTGAGTCTGATGAGGGGGTGAGTGATAAACATACCCAGTCCATTCTTG T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96300976..96301025 26863196 MeRIP-seq:(Medium) rs995570532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776058,Human_RBP_ID_829431,Human_RBP_ID_923287,Human_RBP_ID_1067672,Human_RBP_ID_8852065,Human_RBP_ID_9259873,Human_RBP_ID_9296755,Human_RBP_ID_9384278,Human_RBP_ID_22076475,Human_RBP_ID_24546106,Human_RBP_ID_26338632,Human_RBP_ID_27573258 Human_Splice_Rec_274828,Human_Splice_Rec_274829,Human_Splice_Rec_275008,Human_Splice_Rec_275009 RMVar_hsa_circ_88869,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_201844,RMVar_hsa_circ_78669,RMVar_hsa_circ_201866,RMVar_hsa_circ_77402,RMVar_hsa_circ_201867,RMVar_hsa_circ_41740,RMVar_hsa_circ_43933,RMVar_hsa_circ_67902 71377 RMVar_ID_71377 Human_SNP_ID_83477421 m1A Human chr2 + 96301480 96301477 96301480 AATGATGCTAGAAGATGCATGTTTAGGGGTCAACAACAACCAATGAACATGATCAGAACATAAAG AATGATGCTAGAAGATGCATGTTTAGGGGT___CAACAACCAATGAACATGATCAGAACATAAAG TCAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96301477..96301705 26863196 MeRIP-seq:(Medium) rs1202982351 Functional Loss DEL dbSNP153 31..33 33 - - - 71378 RMVar_ID_71378 Human_SNP_ID_83477424 m1A Human chr2 + 96301480 96301480 96301480 AATGATGCTAGAAGATGCATGTTTAGGGGTCAACAACAACCAATGAACATGATCAGAACATAAAG AATGATGCTAGAAGATGCATGTTTAGGGGTCAGCAACAACCAATGAACATGATCAGAACATAAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96301477..96301705 26863196 MeRIP-seq:(Medium) rs754689189 Functional Loss SNV dbSNP153 33..33 33 - - - 71379 RMVar_ID_71379 Human_SNP_ID_83477425 m1A Human chr2 + 96301480 96301480 96301480 AATGATGCTAGAAGATGCATGTTTAGGGGTCAACAACAACCAATGAACATGATCAGAACATAAAG AATGATGCTAGAAGATGCATGTTTAGGGGTCATCAACAACCAATGAACATGATCAGAACATAAAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96301477..96301705 26863196 MeRIP-seq:(Medium) rs754689189 Functional Loss SNV dbSNP153 33..33 33 - - - 71380 RMVar_ID_71380 Human_SNP_ID_83477438 m1A Human chr2 + 96301502 96301501 96301503 TTAGGGGTCAACAACAACCAATGAACATGATCAGAACATAAAGCGCGCACTTACCCATATTTTGG TTAGGGGTCAACAACAACCAATGAACATGATC__AACATAAAGCGCGCACTTACCCATATTTTGG CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96301501..96301550 26863196 MeRIP-seq:(Medium) rs1558772452 Functional Loss DEL dbSNP153 33..34 33 - - - 71381 RMVar_ID_71381 Human_SNP_ID_83477839 m1A Human chr2 - 96303227 96303227 96303227 TTGATGAGATGGTGGGCATCATCTACAAGCCCAAAACTAAAGAGACTCGGGAGACCTATGAGGTG TTGATGAGATGGTGGGCATCATCTACAAGCCCGAAACTAAAGAGACTCGGGAGACCTATGAGGTG T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96303151..96303250 32194978 MeRIP-seq:(Medium) rs1441814288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776059,Human_RBP_ID_830107,Human_RBP_ID_1591783,Human_RBP_ID_1925221,Human_RBP_ID_3959284,Human_RBP_ID_8527346,Human_RBP_ID_9384284,Human_RBP_ID_24533681,Human_RBP_ID_26339572,Human_RBP_ID_27016561,Human_RBP_ID_27817354 Human_Splice_Rec_274825,Human_Splice_Rec_275005 RMVar_hsa_circ_88869,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_201844,RMVar_hsa_circ_201866,RMVar_hsa_circ_77402,RMVar_hsa_circ_43933,RMVar_hsa_circ_201875,RMVar_hsa_circ_111395 71382 RMVar_ID_71382 Human_SNP_ID_83478212 m1A Human chr2 + 96304669 96304669 96304669 GCTGCTCGAATGTTAAAGGGAAGAGACTTTGGATCTGAAGGAAAAAATAGTATCCCCTTGGCACT GCTGCTCGAATGTTAAAGGGAAGAGACTTTGGGTCTGAAGGAAAAAATAGTATCCCCTTGGCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96304665..96304782 26863196 MeRIP-seq:(Medium) rs780943026 Functional Loss SNV dbSNP153 33..33 33 - - - 71383 RMVar_ID_71383 Human_SNP_ID_83478441 m1A Human chr2 + 96305461 96305461 96305461 ATCCGCCATGGCCGCGGCTGCTCGGAGGCTTCAGACCACCACGCCTCCCTACCGCAAGCTGCAAA ATCCGCCATGGCCGCGGCTGCTCGGAGGCTTCGGACCACCACGCCTCCCTACCGCAAGCTGCAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:96305363..96305525;chr2:96305358..96305525 26863196 MeRIP-seq:(Medium) rs1465840912 Functional Loss SNV dbSNP153 33..33 33 - - - 71384 RMVar_ID_71384 Human_SNP_ID_83485718 m1A Human chr2 - 96335850 96335850 96335850 CCTTCCCGCCGCGCCTCCCGACCGCCCGGCTCACCTGGGCCGGGAGGTCCCATCTTTCCTTGGCG CCTTCCCGCCGCGCCTCCCGACCGCCCGGCTCTCCTGGGCCGGGAGGTCCCATCTTTCCTTGGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:96335819..96335929;chr2:96335801..96335947;chr2:96335817..96335972;chr2:96335801..96335900;chr2:96335801..96335986;chr2:96335818..96335974;chr2:96335817..96335973 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs759106037 Functional Loss SNV dbSNP153 33..33 33 - - - 71385 RMVar_ID_71385 Human_SNP_ID_83485719 m1A Human chr2 - 96335850 96335850 96335850 CCTTCCCGCCGCGCCTCCCGACCGCCCGGCTCACCTGGGCCGGGAGGTCCCATCTTTCCTTGGCG CCTTCCCGCCGCGCCTCCCGACCGCCCGGCTCGCCTGGGCCGGGAGGTCCCATCTTTCCTTGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:96335819..96335929;chr2:96335801..96335947;chr2:96335817..96335972;chr2:96335801..96335900;chr2:96335801..96335986;chr2:96335818..96335974;chr2:96335817..96335973 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs759106037 Functional Loss SNV dbSNP153 33..33 33 - - - 71386 RMVar_ID_71386 Human_SNP_ID_83487175 m1A Human chr2 + 96341629 96341621 96341630 GGAAATGTTCTCTTGAAGGTTTCTTGAGCAAGAATTTTGTTCCAGCACTGCCAGCCACAATGAAT GGAAATGTTCTCTTGAAGGTTTCTT_________TTTTGTTCCAGCACTGCCAGCCACAATGAAT TGAGCAAGAA T NCAPH Ensembl:ENSG00000121152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:96341626..96341871;chr2:96341626..96341812 26863196 MeRIP-seq:(Medium) rs754299019 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_22996409 71387 RMVar_ID_71387 Human_SNP_ID_83487177 m1A Human chr2 + 96341627 96341627 96341627 TAGGAAATGTTCTCTTGAAGGTTTCTTGAGCAAGAATTTTGTTCCAGCACTGCCAGCCACAATGA TAGGAAATGTTCTCTTGAAGGTTTCTTGAGCAGGAATTTTGTTCCAGCACTGCCAGCCACAATGA A G NCAPH Ensembl:ENSG00000121152 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:96341615..96341837 26863410 MeRIP-seq:(Medium) rs746837163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22996409 71388 RMVar_ID_71388 Human_SNP_ID_83488401 m1A Human chr2 + 96346675 96346675 96346675 CTGGTGGGGTCAAAGACTTCGTGGTGTTGGGGACAAGAAGGGGTGAGCTGGAAATGTAGGAGGTG CTGGTGGGGTCAAAGACTTCGTGGTGTTGGGGTCAAGAAGGGGTGAGCTGGAAATGTAGGAGGTG A T NCAPH Ensembl:ENSG00000121152 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96346507..96346735 26863196 MeRIP-seq:(Medium) rs1054121835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14039,RMVar_hsa_circ_201876,RMVar_hsa_circ_101892 71389 RMVar_ID_71389 Human_SNP_ID_83491484 m1A Human chr2 + 96359191 96359191 96359191 CCCGGATCACTGGCGCTTTAGGCCTCGACGCAAACGTATGTAATTCTAGGTGGAATTTTAAGAAA CCCGGATCACTGGCGCTTTAGGCCTCGACGCAGACGTATGTAATTCTAGGTGGAATTTTAAGAAA A G NCAPH Ensembl:ENSG00000121152 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:96359151..96359200 32194978 MeRIP-seq:(Medium) rs747940696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_275089,Human_Splice_Rec_275121,Human_Splice_Rec_275173,Human_Splice_Rec_275207 RMVar_hsa_circ_12734,RMVar_hsa_circ_20526,RMVar_hsa_circ_201876,RMVar_hsa_circ_101892,RMVar_hsa_circ_329440,RMVar_hsa_circ_14978,RMVar_hsa_circ_201878,RMVar_hsa_circ_9410,RMVar_hsa_circ_117120,RMVar_hsa_circ_332299,RMVar_hsa_circ_369827,RMVar_hsa_circ_375728,RMVar_hsa_circ_280273,RMVar_hsa_circ_44094,RMVar_hsa_circ_201880,RMVar_hsa_circ_201881,RMVar_hsa_circ_201882,RMVar_hsa_circ_201879 71390 RMVar_ID_71390 Human_SNP_ID_83494628 m1A Human chr2 + 96372243 96372243 96372243 GCTGGGAGGTAGGTAGGGAAAGGCCTGTGCAGAGACTGGCAGGAGGTCACTGCTGTCAGGAACTA GCTGGGAGGTAGGTAGGGAAAGGCCTGTGCAGGGACTGGCAGGAGGTCACTGCTGTCAGGAACTA A G NCAPH Ensembl:ENSG00000121152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96372239..96372368 26863196 MeRIP-seq:(Medium) rs1218724052 Functional Loss SNV dbSNP153 33..33 33 - - - 71391 RMVar_ID_71391 Human_SNP_ID_83540168 m1A Human chr2 + 96550689 96550689 96550689 TGGCTAAGGAGAACAGGGGGGATGATGGGGCCACCGAGAGGCCGAAGAAGGCCAAGGAGGAGCGG TGGCTAAGGAGAACAGGGGGGATGATGGGGCCGCCGAGAGGCCGAAGAAGGCCAAGGAGGAGCGG A G ARID5A Ensembl:ENSG00000196843 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96550639..96551351 32194978 MeRIP-seq:(Medium) rs989764612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_275277,Human_Splice_Rec_275289,Human_Splice_Rec_275301,Human_Splice_Rec_275309,Human_Splice_Rec_275321,Human_Splice_Rec_275327 RMVar_hsa_circ_20586,RMVar_hsa_circ_83546,RMVar_hsa_circ_201886 71392 RMVar_ID_71392 Human_SNP_ID_83584802 m1A Human chr2 + 96730316 96730316 96730316 ATTTCCTCAGCATGACTACAAATCCAGTCATGATCCTCTCTTCAATAAAATCCTTTAATGTACCT ATTTCCTCAGCATGACTACAAATCCAGTCATGTTCCTCTCTTCAATAAAATCCTTTAATGTACCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:96730313..96730400 26863196 MeRIP-seq:(Medium) rs1410869357 Functional Loss SNV dbSNP153 33..33 33 - - - 71393 RMVar_ID_71393 Human_SNP_ID_83587183 m1A Human chr2 + 96740013 96740013 96740013 AGCCGACAAACATCGCCGCCACTGCTGCCACGACCCAAGGGGTCCCAGAGTCGCCGCCATCTTTC AGCCGACAAACATCGCCGCCACTGCTGCCACGGCCCAAGGGGTCCCAGAGTCGCCGCCATCTTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:96739903..96740050;chr2:96738031..96740050 26863196 MeRIP-seq:(Medium) rs199520249 Functional Loss SNV dbSNP153 33..33 33 - - - 71394 RMVar_ID_71394 Human_SNP_ID_83587185 m1A Human chr2 + 96740017 96740017 96740017 GACAAACATCGCCGCCACTGCTGCCACGACCCAAGGGGTCCCAGAGTCGCCGCCATCTTTCCCAC GACAAACATCGCCGCCACTGCTGCCACGACCCGAGGGGTCCCAGAGTCGCCGCCATCTTTCCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96739819..96740050 26863196 MeRIP-seq:(Medium) rs767534463 Functional Loss SNV dbSNP153 33..33 33 - - - 71395 RMVar_ID_71395 Human_SNP_ID_83592267 m1A Human chr2 + 96760971 96760971 96760971 TGCGGACCGGGGCCGCGCGGCGTGGCGCGGGGAGCGGCGGCGGCGGCAGAGCCAGAGCAACATGG TGCGGACCGGGGCCGCGCGGCGTGGCGCGGGGGGCGGCGGCGGCGGCAGAGCCAGAGCAACATGG A G CNNM4 Ensembl:ENSG00000158158 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:96760922..96761261;chr2:96760927..96761249 26863196 MeRIP-seq:(Medium) rs1275039303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622560,Human_RBP_ID_18421850 71396 RMVar_ID_71396 Human_SNP_ID_83592275 m1A Human chr2 + 96760986 96760986 96760986 CGCGGCGTGGCGCGGGGAGCGGCGGCGGCGGCAGAGCCAGAGCAACATGGCGCCGGTGGGCGGGG CGCGGCGTGGCGCGGGGAGCGGCGGCGGCGGCCGAGCCAGAGCAACATGGCGCCGGTGGGCGGGG A C CNNM4 Ensembl:ENSG00000158158 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96760940..96761140 26863196 MeRIP-seq:(Medium) rs545205153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622560 Clinvar_Rec_297 71397 RMVar_ID_71397 Human_SNP_ID_83602458 m1A Human chr2 + 96801430 96801427 96801431 AGATACACATAGCCATAGATACACGCAGAGACACACACAGTGAGAGACCACATGCAGAGAGACCG AGATACACATAGCCATAGATACACGCAGAG____ACACAGTGAGAGACCACATGCAGAGAGACCG GACAC G CNNM4 Ensembl:ENSG00000158158 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96801425..96801524 26863196 MeRIP-seq:(Medium) rs1343433508 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_204846,Human_RBP_ID_2668932 RMVar_hsa_circ_364572,RMVar_hsa_circ_201906,RMVar_hsa_circ_370820 71398 RMVar_ID_71398 Human_SNP_ID_83606599 m1A Human chr2 - 96816308 96816308 96816308 GCCCAGGCAGAGCGCGGCGAACAACCAGCCTAACCGACCCGCCGCAGCTACCGCCGCCGCCATCG GCCCAGGCAGAGCGCGGCGAACAACCAGCCTACCCGACCCGCCGCAGCTACCGCCGCCGCCATCG T G CNNM3-DT RNACentral:URS00008BB4F7 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96816244..96816691 26863196 MeRIP-seq:(Medium) rs1178632215 Functional Loss SNV dbSNP153 33..33 33 - - - 71399 RMVar_ID_71399 Human_SNP_ID_83606601 m1A Human chr2 - 96816318 96816315 96816318 CCGCGGCGTTGCCCAGGCAGAGCGCGGCGAACAACCAGCCTAACCGACCCGCCGCAGCTACCGCC CCGCGGCGTTGCCCAGGCAGAGCGCGGCGAAC___CAGCCTAACCGACCCGCCGCAGCTACCGCC GGTT G CNNM3-DT RNACentral:URS00008BB4F7 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:96816269..96816548 26863196 MeRIP-seq:(Medium) rs1559004309 Functional Loss DEL dbSNP153 33..35 33 - - - 71400 RMVar_ID_71400 Human_SNP_ID_83606939 m1A Human chr2 - 96817050 96817050 96817050 CGGGCAGAGTGAGCAGGACGGCCAGGCGGCTGAGGCCGAGCGCTCGCGGCGCCAGCGCCAGCGTC CGGGCAGAGTGAGCAGGACGGCCAGGCGGCTGGGGCCGAGCGCTCGCGGCGCCAGCGCCAGCGTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:96816951..96817110 26863410 MeRIP-seq:(Medium) rs1413054953 Functional Loss SNV dbSNP153 33..33 33 - - - 71401 RMVar_ID_71401 Human_SNP_ID_83608030 m1A Human chr2 + 96820549 96820549 96820549 GAAGCCCAGGAGAAGCTGGCCAGGAGGAGGCAAGACCAAGGAAGGAGGAGTTCCCGAGATGCGGA GAAGCCCAGGAGAAGCTGGCCAGGAGGAGGCAGGACCAAGGAAGGAGGAGTTCCCGAGATGCGGA A G CNNM3 Ensembl:ENSG00000168763 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96820524..96820599 26863196 MeRIP-seq:(Medium) rs1485401492 Functional Loss SNV dbSNP153 33..33 33 - - - 71402 RMVar_ID_71402 Human_SNP_ID_83610454 m1A Human chr2 + 96829045 96829045 96829045 CCTCAATGCACTCCTGGCTACCCGAGCCCAGAACCTGCCACAGTCCCCTGAGAACACCGACCTGC CCTCAATGCACTCCTGGCTACCCGAGCCCAGACCCTGCCACAGTCCCCTGAGAACACCGACCTGC A C CNNM3 Ensembl:ENSG00000168763 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96828964..96829064 26863196 MeRIP-seq:(Medium) rs758128177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13992236 Human_Splice_Rec_276512,Human_Splice_Rec_276513,Human_Splice_Rec_276526,Human_Splice_Rec_276527,Human_Splice_Rec_276533,Human_Splice_Rec_276538,Human_Splice_Rec_276539 RMVar_hsa_circ_326413,RMVar_hsa_circ_77188,RMVar_hsa_circ_324375,RMVar_hsa_circ_201910,RMVar_hsa_circ_201911,RMVar_hsa_circ_377870,RMVar_hsa_circ_56716,RMVar_hsa_circ_316520 71403 RMVar_ID_71403 Human_SNP_ID_83610455 m1A Human chr2 + 96829045 96829045 96829045 CCTCAATGCACTCCTGGCTACCCGAGCCCAGAACCTGCCACAGTCCCCTGAGAACACCGACCTGC CCTCAATGCACTCCTGGCTACCCGAGCCCAGAGCCTGCCACAGTCCCCTGAGAACACCGACCTGC A G CNNM3 Ensembl:ENSG00000168763 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96828964..96829064 26863196 MeRIP-seq:(Medium) rs758128177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13992236 Human_Splice_Rec_276512,Human_Splice_Rec_276513,Human_Splice_Rec_276526,Human_Splice_Rec_276527,Human_Splice_Rec_276533,Human_Splice_Rec_276538,Human_Splice_Rec_276539 RMVar_hsa_circ_326413,RMVar_hsa_circ_77188,RMVar_hsa_circ_324375,RMVar_hsa_circ_201910,RMVar_hsa_circ_201911,RMVar_hsa_circ_377870,RMVar_hsa_circ_56716,RMVar_hsa_circ_316520 71404 RMVar_ID_71404 Human_SNP_ID_83613525 m1A Human chr2 - 96839615 96839615 96839615 CAGGCCTCCGTGACCCCGGTGCAGCTGGCTCGAGACTGGCAGCGCGGCATCCGGGAGGCCCTGCA CAGGCCTCCGTGACCCCGGTGCAGCTGGCTCGGGACTGGCAGCGCGGCATCCGGGAGGCCCTGCA T C ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding 3'UTR,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs771412496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22595839 Human_Splice_Rec_276572,Human_Splice_Rec_276588,Human_Splice_Rec_276604,Human_Splice_Rec_276612 71405 RMVar_ID_71405 Human_SNP_ID_83613526 m1A Human chr2 - 96839615 96839615 96839615 CAGGCCTCCGTGACCCCGGTGCAGCTGGCTCGAGACTGGCAGCGCGGCATCCGGGAGGCCCTGCA CAGGCCTCCGTGACCCCGGTGCAGCTGGCTCGCGACTGGCAGCGCGGCATCCGGGAGGCCCTGCA T G ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding 3'UTR,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs771412496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22595839 Human_Splice_Rec_276572,Human_Splice_Rec_276588,Human_Splice_Rec_276604,Human_Splice_Rec_276612 71406 RMVar_ID_71406 Human_SNP_ID_83613975 m1A Human chr2 - 96840535 96840535 96840535 GTCTCTAGGGGTGGCTGCACTCCCTCTGCCTAATCTTCCATCTCTGCCCTCAGCTCCACCGCACC GTCTCTAGGGGTGGCTGCACTCCCTCTGCCTAGTCTTCCATCTCTGCCCTCAGCTCCACCGCACC T C ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96840532..96840620 26863196 MeRIP-seq:(Medium) rs1419225061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5378593,Human_RBP_ID_19101090,Human_RBP_ID_22548395,Human_RBP_ID_22595841,Human_RBP_ID_22667567,Human_RBP_ID_22742712,Human_RBP_ID_26787080 71407 RMVar_ID_71407 Human_SNP_ID_83614548 m1A Human chr2 - 96842317 96842317 96842317 GGGCCGGGGTTGGGGGCAGTGGCTAATCCCTGAGGCCGGCTGAGCAGTGAGGCCTGGAGGGACTC GGGCCGGGGTTGGGGGCAGTGGCTAATCCCTGTGGCCGGCTGAGCAGTGAGGCCTGGAGGGACTC T A ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:96842316..96842458 26863196 MeRIP-seq:(Medium) rs1456876548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36388,RMVar_hsa_circ_310403 71408 RMVar_ID_71408 Human_SNP_ID_83616181 m1A Human chr2 - 96848391 96848391 96848391 GACATCTGCTCCCTCCTCCTGCAACACAGCCCAGCCCTGAAGGCCATCCGGGACCGAAAGGCACG GACATCTGCTCCCTCCTCCTGCAACACAGCCCGGCCCTGAAGGCCATCCGGGACCGAAAGGCACG T C ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96848341..96848441 32194978 MeRIP-seq:(Medium) rs775403383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_276614,Human_Splice_Rec_276632,Human_Splice_Rec_276648 Human_miRNA_ID_1158440 RMVar_hsa_circ_36388,RMVar_hsa_circ_23182 71409 RMVar_ID_71409 Human_SNP_ID_83619403 m1A Human chr2 + 96860302 96860302 96860302 ACAAGCGCGCACGCGCGTGCACACACACATACACACACACACAAACACATGTGCAAATACAGACA ACAAGCGCGCACGCGCGTGCACACACACATACGCACACACACAAACACATGTGCAAATACAGACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:96860211..96860312 32194978 MeRIP-seq:(Medium) rs1452184316 Functional Loss SNV dbSNP153 33..33 33 - - - 71410 RMVar_ID_71410 Human_SNP_ID_83619455 m1A Human chr2 + 96860461 96860461 96860461 GGCTGGTGCCCTGGTGAGCCACACCAAGTGGCAGTGCCCGTGCTGAGCAGAGCAGGTCCTCATGG GGCTGGTGCCCTGGTGAGCCACACCAAGTGGCGGTGCCCGTGCTGAGCAGAGCAGGTCCTCATGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96860410..96861454 32194978 MeRIP-seq:(Medium) rs1277891548 Functional Loss SNV dbSNP153 33..33 33 - - - 71411 RMVar_ID_71411 Human_SNP_ID_83620470 m1A Human chr2 + 96863328 96863328 96863328 CCACCATGGTGAGGGCATCATAAACATCTCACAGCCTGGGAGGTCTGGTCACAGGGGCATGGTCA CCACCATGGTGAGGGCATCATAAACATCTCACGGCCTGGGAGGTCTGGTCACAGGGGCATGGTCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96863327..96864060 32194978 MeRIP-seq:(Medium) rs997447084 Functional Loss SNV dbSNP153 33..33 33 - - - 71412 RMVar_ID_71412 Human_SNP_ID_83621101 m1A Human chr2 + 96865319 96865319 96865319 AAGTTGTTGAGTGTGGCCGAGTACAGCTCACCATCTATGGGAGACAGAGGTCAGCTAGGCCACAC AAGTTGTTGAGTGTGGCCGAGTACAGCTCACCGTCTATGGGAGACAGAGGTCAGCTAGGCCACAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:96865286..96865684 32194978 MeRIP-seq:(Medium) rs757927199 Functional Loss SNV dbSNP153 33..33 33 - - - 71413 RMVar_ID_71413 Human_SNP_ID_83621900 m1A Human chr2 - 96867878 96867878 96867878 AAGCTCAGAGCCGGGGCGTGCGCCATGGCCCCACACTGGGCTGTCTGGCTGCTGGCAGCAAGGCT AAGCTCAGAGCCGGGGCGTGCGCCATGGCCCCCCACTGGGCTGTCTGGCTGCTGGCAGCAAGGCT T G SEMA4C Ensembl:ENSG00000168758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96867833..96867955 26863196 MeRIP-seq:(Medium) rs765105568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9298,Human_RBP_ID_4622568,Human_RBP_ID_5379681,Human_RBP_ID_18493385,Human_RBP_ID_22548399,Human_RBP_ID_22669270,Human_RBP_ID_22743213,Human_RBP_ID_26786266 Human_Splice_Rec_276650,Human_Splice_Rec_276708,Human_Splice_Rec_276720 RMVar_hsa_circ_357006,RMVar_hsa_circ_355165 71414 RMVar_ID_71414 Human_SNP_ID_83622505 m1A Human chr2 - 96870033 96870033 96870033 GCCCGCCGTGGTGGCGCGGGGAGCCCGAGCCTAGGGGCGCGGAGCCGGGCGGGGACGGAGGGGCG GCCCGCCGTGGTGGCGCGGGGAGCCCGAGCCTGGGGGCGCGGAGCCGGGCGGGGACGGAGGGGCG T C SEMA4C Ensembl:ENSG00000168758 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96869814..96870100 26863196 MeRIP-seq:(Medium) rs984927307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4621564,Human_RBP_ID_17392997,Human_RBP_ID_27840051 71415 RMVar_ID_71415 Human_SNP_ID_83622506 m1A Human chr2 - 96870033 96870033 96870033 GCCCGCCGTGGTGGCGCGGGGAGCCCGAGCCTAGGGGCGCGGAGCCGGGCGGGGACGGAGGGGCG GCCCGCCGTGGTGGCGCGGGGAGCCCGAGCCTCGGGGCGCGGAGCCGGGCGGGGACGGAGGGGCG T G SEMA4C Ensembl:ENSG00000168758 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96869814..96870100 26863196 MeRIP-seq:(Medium) rs984927307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4621564,Human_RBP_ID_17392997,Human_RBP_ID_27840051 71416 RMVar_ID_71416 Human_SNP_ID_83683982 m1A Human chr2 - 97113666 97113666 97113666 TCGCCTTCGGGGATCGCCGCCTCCGAAGAGCAACAACGAGCAAAGCAGTCTGTCCACGGACCTCC TCGCCTTCGGGGATCGCCGCCTCCGAAGAGCAGCAACGAGCAAAGCAGTCTGTCCACGGACCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:97113620..97113750;chr2:97113615..97113867;chr2:97113615..97113720 26863196 MeRIP-seq:(Medium) rs879606714 Functional Loss SNV dbSNP153 33..33 33 - - - 71417 RMVar_ID_71417 Human_SNP_ID_83683997 m1A Human chr2 - 97113706 97113706 97113706 ATCGTCGGCTGCAAATTGTAGCCTGCAGCCGTATTTCAGCTCGCCTTCGGGGATCGCCGCCTCCG ATCGTCGGCTGCAAATTGTAGCCTGCAGCCGTCTTTCAGCTCGCCTTCGGGGATCGCCGCCTCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:97113659..97113765 26863196 MeRIP-seq:(Medium) rs1336938778 Functional Loss SNV dbSNP153 33..33 33 - - - 71418 RMVar_ID_71418 Human_SNP_ID_83684017 m1A Human chr2 + 97113740 97113740 97113740 CGGCTGCAGGCTACAATTTGCAGCCGACGATTATGGAAGACGGCAAGCGGGAGAGGTGGCCCACC CGGCTGCAGGCTACAATTTGCAGCCGACGATTGTGGAAGACGGCAAGCGGGAGAGGTGGCCCACC A G ANKRD36 Ensembl:ENSG00000135976 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:97113643..97113769 26863196 MeRIP-seq:(Medium) rs747515638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_305484,Human_RBP_ID_774334,Human_RBP_ID_4621592,Human_RBP_ID_22076509,Human_RBP_ID_27818743 RMVar_hsa_circ_76528,RMVar_hsa_circ_201943 71419 RMVar_ID_71419 Human_SNP_ID_83768993 m1A Human chr2 - 97646185 97646185 97646185 TCCCTGGCACGCCCGGAGACCCGAGTACCTCCAGATGCCATGGAGCGCATCGCGGCCGCGCCACT TCCCTGGCACGCCCGGAGACCCGAGTACCTCCCGATGCCATGGAGCGCATCGCGGCCGCGCCACT T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:97646121..97646210 26863410 MeRIP-seq:(Medium) rs756384067 Functional Loss SNV dbSNP153 33..33 33 - - - 71420 RMVar_ID_71420 Human_SNP_ID_83769257 m1A Human chr2 + 97647055 97647055 97647055 CAGTCATTTCAGTCAGCGTCATAATTCACGTTATCTTCCTTTAGGTGGTGTTCCCACTGATGAAG CAGTCATTTCAGTCAGCGTCATAATTCACGTTGTCTTCCTTTAGGTGGTGTTCCCACTGATGAAG A G COX5B Ensembl:ENSG00000135940 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:97647051..97647175 26863410 MeRIP-seq:(Medium) rs765221605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5377912,Human_RBP_ID_19101113,Human_RBP_ID_22598530,Human_RBP_ID_22667626,Human_RBP_ID_25573314 Human_Splice_Rec_277889,Human_Splice_Rec_277897,Human_Splice_Rec_277905,Human_Splice_Rec_277909 RMVar_hsa_circ_82754,RMVar_hsa_circ_201980 71421 RMVar_ID_71421 Human_SNP_ID_83769336 m1A Human chr2 + 97647298 97647298 97647298 TGGAAGGTAGGGCTTATTTGGCCTAATGGTTCAATTCTTGTTTTTTTTGTTTTGTTTTGTTTTTT TGGAAGGTAGGGCTTATTTGGCCTAATGGTTCGATTCTTGTTTTTTTTGTTTTGTTTTGTTTTTT A G COX5B Ensembl:ENSG00000135940 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:97647295..97647469 26863196 MeRIP-seq:(Medium) rs1192414963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82754,RMVar_hsa_circ_117658,RMVar_hsa_circ_201980,RMVar_hsa_circ_201981 71422 RMVar_ID_71422 Human_SNP_ID_83769371 m1A Human chr2 + 97647351 97647351 97647351 GTTTTGTTTTTTGTTTTTTCTTCAGGACCCATACAATGTACTGGCCCCAAAGGGAGCTTCAGGCA GTTTTGTTTTTTGTTTTTTCTTCAGGACCCATGCAATGTACTGGCCCCAAAGGGAGCTTCAGGCA A G COX5B Ensembl:ENSG00000135940 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:97647051..97648175 32194978 MeRIP-seq:(Medium) rs1276785184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558400,Human_RBP_ID_775722,Human_RBP_ID_829277,Human_RBP_ID_921653,Human_RBP_ID_1024671,Human_RBP_ID_4621605,Human_RBP_ID_5118005,Human_RBP_ID_6959952,Human_RBP_ID_17657457,Human_RBP_ID_17963541,Human_RBP_ID_18470829,Human_RBP_ID_22449946,Human_RBP_ID_22667627,Human_RBP_ID_27293916 Human_Splice_Rec_277890,Human_Splice_Rec_277891,Human_Splice_Rec_277898,Human_Splice_Rec_277899,Human_Splice_Rec_277906,Human_Splice_Rec_277907,Human_Splice_Rec_277910 Human_miRNA_ID_2661155,Human_miRNA_ID_2678253,Human_miRNA_ID_2679608,Human_miRNA_ID_3080301 RMVar_hsa_circ_100392,RMVar_hsa_circ_82754,RMVar_hsa_circ_117658,RMVar_hsa_circ_201980,RMVar_hsa_circ_201981,RMVar_hsa_circ_201982 71423 RMVar_ID_71423 Human_SNP_ID_83772762 m1A Human chr2 - 97659515 97659515 97659515 GCTTCCAGGAGGGCGGAAAGCAGCCGCTGAGCAAGGGCCGGGTGCCACACCTCCCTTCCCACCCC GCTTCCAGGAGGGCGGAAAGCAGCCGCTGAGCCAGGGCCGGGTGCCACACCTCCCTTCCCACCCC T G ACTR1B Ensembl:ENSG00000115073 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:97659509..97659652 26863196 MeRIP-seq:(Medium) rs1257150522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4621660,Human_RBP_ID_22547462,Human_RBP_ID_22667634,Human_RBP_ID_26786298 RMVar_hsa_circ_42571,RMVar_hsa_circ_344746,RMVar_hsa_circ_367825 71424 RMVar_ID_71424 Human_SNP_ID_83798907 m1A Human chr2 + 97763531 97763531 97763531 CACTCAGGACGTGTCTCACACCGCTCTCCCATACGAGCCCTGCTCGAATCTTTGTCCCCATCAAG CACTCAGGACGTGTCTCACACCGCTCTCCCATGCGAGCCCTGCTCGAATCTTTGTCCCCATCAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:97763375..97763639 26863196 MeRIP-seq:(Medium) rs926419145 Functional Loss SNV dbSNP153 33..33 33 - - - 71425 RMVar_ID_71425 Human_SNP_ID_83963219 m1A Human chr2 - 98444933 98444933 98444933 TCAGGTGCTGGTCCTCCTGCCCCGGCCCACGGAGCCCGACCCGGCGGCAAACCAGCAGCGAACCC TCAGGTGCTGGTCCTCCTGCCCCGGCCCACGGGGCCCGACCCGGCGGCAAACCAGCAGCGAACCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:98444882..98445053 26863196 MeRIP-seq:(Medium) rs1165297267 Functional Loss SNV dbSNP153 33..33 33 - - - 71426 RMVar_ID_71426 Human_SNP_ID_83963222 m1A Human chr2 - 98444937 98444937 98444937 GGCCTCAGGTGCTGGTCCTCCTGCCCCGGCCCACGGAGCCCGACCCGGCGGCAAACCAGCAGCGA GGCCTCAGGTGCTGGTCCTCCTGCCCCGGCCCGCGGAGCCCGACCCGGCGGCAAACCAGCAGCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:98444887..98445071 26863196 MeRIP-seq:(Medium) rs894501907 Functional Loss SNV dbSNP153 33..33 33 - - - 71427 RMVar_ID_71427 Human_SNP_ID_83987690 m1A Human chr2 + 98547635 98547635 98547635 GGAAGTAGCATGAGGTGTTTGGTTTAGGGAGAATAATTATGACTTAGCATGTGTTTGGGCTGATA GGAAGTAGCATGAGGTGTTTGGTTTAGGGAGAGTAATTATGACTTAGCATGTGTTTGGGCTGATA A G INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98547597..98548039 26863196 MeRIP-seq:(Medium) rs749934379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9291,RMVar_hsa_circ_18622,RMVar_hsa_circ_340547,RMVar_hsa_circ_107765,RMVar_hsa_circ_202032,RMVar_hsa_circ_55707,RMVar_hsa_circ_202037,RMVar_hsa_circ_28183,RMVar_hsa_circ_2643,RMVar_hsa_circ_46590,RMVar_hsa_circ_108799,RMVar_hsa_circ_359690,RMVar_hsa_circ_93337,RMVar_hsa_circ_202040,RMVar_hsa_circ_15436,RMVar_hsa_circ_202041,RMVar_hsa_circ_125347,RMVar_hsa_circ_202042,RMVar_hsa_circ_70933 71428 RMVar_ID_71428 Human_SNP_ID_83993291 m1A Human chr2 - 98570517 98570517 98570517 CTTTGGGACAAAGTGGTCCATTCCAGGGCAGCACCATTTCATCACCCCTTGATCCCTGGCCCAGC CTTTGGGACAAAGTGGTCCATTCCAGGGCAGCGCCATTTCATCACCCCTTGATCCCTGGCCCAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:98570509..98570804 26863196 MeRIP-seq:(Medium) rs952736896 Functional Loss SNV dbSNP153 33..33 33 - - - 71429 RMVar_ID_71429 Human_SNP_ID_83993323 m1A Human chr2 + 98570673 98570673 98570673 GGAGAACACACAGGGCTGGAAGATGCAAGAGGACACCAGAGTCACAGACCAGGCCCTGGAGTGGG GGAGAACACACAGGGCTGGAAGATGCAAGAGGTCACCAGAGTCACAGACCAGGCCCTGGAGTGGG A T INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98569854..98570827 26863196 MeRIP-seq:(Medium) rs946465484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13996922 RMVar_hsa_circ_968,RMVar_hsa_circ_9291,RMVar_hsa_circ_340547,RMVar_hsa_circ_107765,RMVar_hsa_circ_202032,RMVar_hsa_circ_202037,RMVar_hsa_circ_2643,RMVar_hsa_circ_359690,RMVar_hsa_circ_125347,RMVar_hsa_circ_202042,RMVar_hsa_circ_87314,RMVar_hsa_circ_202044,RMVar_hsa_circ_9797,RMVar_hsa_circ_119314,RMVar_hsa_circ_202047,RMVar_hsa_circ_72417,RMVar_hsa_circ_37059,RMVar_hsa_circ_369410,RMVar_hsa_circ_202048,RMVar_hsa_circ_327979,RMVar_hsa_circ_202050,RMVar_hsa_circ_265000 71430 RMVar_ID_71430 Human_SNP_ID_84000518 m1A Human chr2 - 98600130 98600130 98600130 CATCATCTTCGGACTGTTTTTGTTTCCTGGTTACATTTTCAGTCTGGCCCGCTCTACATAATGGG CATCATCTTCGGACTGTTTTTGTTTCCTGGTTTCATTTTCAGTCTGGCCCGCTCTACATAATGGG T A COA5 Ensembl:ENSG00000183513 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72823794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2669526,Human_RBP_ID_17277380,Human_RBP_ID_22506090 GWAS_ID_8450,GWAS_ID_8451,GWAS_ID_8452,GWAS_ID_8453,GWAS_ID_8454,GWAS_ID_8455,GWAS_ID_8456,GWAS_ID_8457,GWAS_ID_8458,GWAS_ID_8459,GWAS_ID_8460,GWAS_ID_8461,GWAS_ID_8462,GWAS_ID_8463,GWAS_ID_8464,GWAS_ID_8465,GWAS_ID_8466,GWAS_ID_8467,GWAS_ID_8468,GWAS_ID_8469,GWAS_ID_8470,GWAS_ID_8471,GWAS_ID_8472,GWAS_ID_8473,GWAS_ID_8474,GWAS_ID_8475,GWAS_ID_8476,GWAS_ID_8477,GWAS_ID_8478,GWAS_ID_8479,GWAS_ID_8480,GWAS_ID_8481,GWAS_ID_8482,GWAS_ID_8483,GWAS_ID_8484,GWAS_ID_8485,GWAS_ID_8486,GWAS_ID_8487,GWAS_ID_8488,GWAS_ID_8489,GWAS_ID_8490,GWAS_ID_8491,GWAS_ID_8492,GWAS_ID_8493,GWAS_ID_8494,GWAS_ID_8495,GWAS_ID_8496,GWAS_ID_8497,GWAS_ID_8498,GWAS_ID_8499,GWAS_ID_8500,GWAS_ID_8501,GWAS_ID_8502,GWAS_ID_8503,GWAS_ID_8504,GWAS_ID_8505,GWAS_ID_8506,GWAS_ID_8507,GWAS_ID_8508,GWAS_ID_8509,GWAS_ID_8510,GWAS_ID_8511,GWAS_ID_8512,GWAS_ID_8513,GWAS_ID_8514,GWAS_ID_8515,GWAS_ID_8516,GWAS_ID_8517,GWAS_ID_8518,GWAS_ID_8519,GWAS_ID_8520,GWAS_ID_8521,GWAS_ID_8522,GWAS_ID_8523,GWAS_ID_8524,GWAS_ID_8525,GWAS_ID_8526,GWAS_ID_8527,GWAS_ID_8528,GWAS_ID_8529,GWAS_ID_8530,GWAS_ID_8531,GWAS_ID_8532,GWAS_ID_8533,GWAS_ID_8534,GWAS_ID_8535,GWAS_ID_8536,GWAS_ID_8537,GWAS_ID_8538,GWAS_ID_8539,GWAS_ID_8540,GWAS_ID_8541,GWAS_ID_8542,GWAS_ID_8543,GWAS_ID_8544,GWAS_ID_8545,GWAS_ID_8546,GWAS_ID_8547,GWAS_ID_8548,GWAS_ID_8549,GWAS_ID_8550,GWAS_ID_8551,GWAS_ID_8552,GWAS_ID_8553,GWAS_ID_8554,GWAS_ID_8555,GWAS_ID_8556,GWAS_ID_8557,GWAS_ID_8558,GWAS_ID_8559,GWAS_ID_8560,GWAS_ID_8561,GWAS_ID_8562,GWAS_ID_8563,GWAS_ID_8564,GWAS_ID_8565,GWAS_ID_8566,GWAS_ID_8567,GWAS_ID_8568,GWAS_ID_8569,GWAS_ID_8570,GWAS_ID_8571,GWAS_ID_8572,GWAS_ID_8573,GWAS_ID_8574,GWAS_ID_8575,GWAS_ID_8576,GWAS_ID_8577,GWAS_ID_8578,GWAS_ID_8579,GWAS_ID_8580,GWAS_ID_8581,GWAS_ID_8582,GWAS_ID_8583,GWAS_ID_8584,GWAS_ID_8585,GWAS_ID_8586,GWAS_ID_8587,GWAS_ID_8588,GWAS_ID_8589,GWAS_ID_8590,GWAS_ID_8591,GWAS_ID_8592,GWAS_ID_8593,GWAS_ID_8594,GWAS_ID_8595,GWAS_ID_8596,GWAS_ID_8597,GWAS_ID_8598,GWAS_ID_8599,GWAS_ID_8600,GWAS_ID_8601,GWAS_ID_8602,GWAS_ID_8603,GWAS_ID_8604,GWAS_ID_8605,GWAS_ID_8606,GWAS_ID_8607,GWAS_ID_8608,GWAS_ID_8609,GWAS_ID_8610,GWAS_ID_8611,GWAS_ID_8612,GWAS_ID_8613,GWAS_ID_8614,GWAS_ID_8615,GWAS_ID_8616,GWAS_ID_8617,GWAS_ID_8618,GWAS_ID_8619,GWAS_ID_8620,GWAS_ID_8621,GWAS_ID_8622,GWAS_ID_8623,GWAS_ID_8624,GWAS_ID_8625,GWAS_ID_8626,GWAS_ID_8627,GWAS_ID_8628,GWAS_ID_8629,GWAS_ID_8630,GWAS_ID_8631,GWAS_ID_8632,GWAS_ID_8633,GWAS_ID_8634,GWAS_ID_8635,GWAS_ID_8636,GWAS_ID_8637,GWAS_ID_8638,GWAS_ID_8639,GWAS_ID_8640,GWAS_ID_8641,GWAS_ID_8642,GWAS_ID_8643,GWAS_ID_8644,GWAS_ID_8645,GWAS_ID_8646,GWAS_ID_8647,GWAS_ID_8648,GWAS_ID_8649,GWAS_ID_8650,GWAS_ID_8651,GWAS_ID_8652,GWAS_ID_8653,GWAS_ID_8654,GWAS_ID_8655,GWAS_ID_8656,GWAS_ID_8657,GWAS_ID_8658,GWAS_ID_8659,GWAS_ID_8660,GWAS_ID_8661,GWAS_ID_8662,GWAS_ID_8663,GWAS_ID_8664,GWAS_ID_8665,GWAS_ID_8666,GWAS_ID_8667,GWAS_ID_8668,GWAS_ID_8669,GWAS_ID_8670,GWAS_ID_8671,GWAS_ID_8672,GWAS_ID_8673,GWAS_ID_8674,GWAS_ID_8675,GWAS_ID_8676,GWAS_ID_8677,GWAS_ID_8678,GWAS_ID_8679,GWAS_ID_8680,GWAS_ID_8681,GWAS_ID_8682,GWAS_ID_8683,GWAS_ID_8684,GWAS_ID_8685,GWAS_ID_8686,GWAS_ID_8687 71431 RMVar_ID_71431 Human_SNP_ID_84001544 m1A Human chr2 - 98604189 98604189 98604189 TGTTTATATTGTTTTATGTGTCTGTCATAGGAAGGAAAATCACCTCGGCAGTGTTTGAAGGAAGG TGTTTATATTGTTTTATGTGTCTGTCATAGGACGGAAAATCACCTCGGCAGTGTTTGAAGGAAGG T G COA5 Ensembl:ENSG00000183513 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:98604101..98604232 26863196 MeRIP-seq:(Medium) rs371263909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22667646,Human_RBP_ID_23891046,Human_RBP_ID_25573725 Human_Splice_Rec_279342,Human_Splice_Rec_279343,Human_Splice_Rec_279345,Human_Splice_Rec_279348,Human_Splice_Rec_279349,Human_Splice_Rec_279351,Human_Splice_Rec_279354,Human_Splice_Rec_279355 71432 RMVar_ID_71432 Human_SNP_ID_84001545 m1A Human chr2 - 98604193 98604193 98604193 AAGGTGTTTATATTGTTTTATGTGTCTGTCATAGGAAGGAAAATCACCTCGGCAGTGTTTGAAGG AAGGTGTTTATATTGTTTTATGTGTCTGTCATTGGAAGGAAAATCACCTCGGCAGTGTTTGAAGG T A COA5 Ensembl:ENSG00000183513 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:98604151..98604200 26863196 MeRIP-seq:(Medium) rs957506507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22667646,Human_RBP_ID_25573725,Human_RBP_ID_27016979 Human_Splice_Rec_279343,Human_Splice_Rec_279345,Human_Splice_Rec_279349,Human_Splice_Rec_279351,Human_Splice_Rec_279355 71433 RMVar_ID_71433 Human_SNP_ID_84002099 m1A Human chr2 - 98606792 98606792 98606792 CAGGTGTGAAGGCCTGTATGTGTGTCAGAGTGAGGAGACTGGATTTTATCCAGACGTTCAGCATC CAGGTGTGAAGGCCTGTATGTGTGTCAGAGTGGGGAGACTGGATTTTATCCAGACGTTCAGCATC T C COA5 Ensembl:ENSG00000183513 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:98606789..98606954 26863196 MeRIP-seq:(Medium) rs1035138679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10000778,Human_RBP_ID_23891055 71434 RMVar_ID_71434 Human_SNP_ID_84002108 m1A Human chr2 + 98606808 98606808 98606808 ATAAAATCCAGTCTCCTCACTCTGACACACATACAGGCCTTCACACCTGGCTGCAACCTTCCCCT ATAAAATCCAGTCTCCTCACTCTGACACACATGCAGGCCTTCACACCTGGCTGCAACCTTCCCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:98606806..98606957 26863196 MeRIP-seq:(Medium) rs1393802042 Functional Loss SNV dbSNP153 33..33 33 - - - 71435 RMVar_ID_71435 Human_SNP_ID_84002562 m1A Human chr2 + 98608430 98608430 98608430 TTAGGCATGACGGCGCTTCCCCTCCGATGCGGACGCGACTTTCTCCCACCGCAACACTTGCAACC TTAGGCATGACGGCGCTTCCCCTCCGATGCGGGCGCGACTTTCTCCCACCGCAACACTTGCAACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:98608276..98608500;chr2:98608262..98608477;chr2:98608156..98608500;chr2:98608220..98608500 26863196 MeRIP-seq:(Medium) rs896544312 Functional Loss SNV dbSNP153 33..33 33 - - - 71436 RMVar_ID_71436 Human_SNP_ID_84002703 m1A Human chr2 - 98608668 98608668 98608668 ACGTCCGAACCAGCCCACCACCTCCTCCCAGCAGCCGACCCCAGCCGCCACCGGGCGGGCTTCCC ACGTCCGAACCAGCCCACCACCTCCTCCCAGCTGCCGACCCCAGCCGCCACCGGGCGGGCTTCCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:98608576..98608750 26863196 MeRIP-seq:(Medium) rs571233345 Functional Loss SNV dbSNP153 33..33 33 - - - 71437 RMVar_ID_71437 Human_SNP_ID_84002704 m1A Human chr2 + 98608675 98608675 98608675 CCGCCCGGTGGCGGCTGGGGTCGGCTGCTGGGAGGAGGTGGTGGGCTGGTTCGGACGTGGGTCGA CCGCCCGGTGGCGGCTGGGGTCGGCTGCTGGGGGGAGGTGGTGGGCTGGTTCGGACGTGGGTCGA A G UNC50 Ensembl:ENSG00000115446 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:98608626..98608766 26863196 MeRIP-seq:(Medium) rs897776687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558569,Human_RBP_ID_4621830,Human_RBP_ID_5502779,Human_RBP_ID_8850922,Human_RBP_ID_9330605,Human_RBP_ID_9353896,Human_RBP_ID_9428761,Human_RBP_ID_18421853,Human_RBP_ID_18443952,Human_RBP_ID_22449948,Human_RBP_ID_27840068 Human_Splice_Rec_279357 71438 RMVar_ID_71438 Human_SNP_ID_84003007 m1A Human chr2 + 98609686 98609685 98609686 ACATGGAAAGTGACCTCCCTGCCAAATAACTCAGAAGAGGAGTGTCGGTAGCCAAATGTTTCTTC ACATGGAAAGTGACCTCCCTGCCAAATAACTC_GAAGAGGAGTGTCGGTAGCCAAATGTTTCTTC CA C UNC50 Ensembl:ENSG00000115446 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:98609685..98609800 26863196 MeRIP-seq:(Medium) rs757696824 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_558570,Human_RBP_ID_1925688,Human_RBP_ID_24560382 Human_Splice_Rec_279376 71439 RMVar_ID_71439 Human_SNP_ID_84004160 m1A Human chr2 - 98614377 98614377 98614377 GCATCTGCTGCTTCCTCAGTCATCTAAGCCAAAATCTTACAGGTCATCCCAAAGGAGCCTCCCAC GCATCTGCTGCTTCCTCAGTCATCTAAGCCAACATCTTACAGGTCATCCCAAAGGAGCCTCCCAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:98614149..98614414 26863196 MeRIP-seq:(Medium) rs527639873 Functional Loss SNV dbSNP153 33..33 33 - - - 71440 RMVar_ID_71440 Human_SNP_ID_84006357 m1A Human chr2 - 98622701 98622701 98622701 CTGCAGCTCATACTGCTCATCTGTCCTCTCCTATGGTGGGTGCTCAGGGCCTCTCACTGTTAGTT CTGCAGCTCATACTGCTCATCTGTCCTCTCCTGTGGTGGGTGCTCAGGGCCTCTCACTGTTAGTT T C MGAT4A Ensembl:ENSG00000071073 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72825704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558636 GWAS_ID_8688,GWAS_ID_8689,GWAS_ID_8690,GWAS_ID_8691,GWAS_ID_8692,GWAS_ID_8693,GWAS_ID_8694,GWAS_ID_8695,GWAS_ID_8696,GWAS_ID_8697,GWAS_ID_8698,GWAS_ID_8699,GWAS_ID_8700,GWAS_ID_8701,GWAS_ID_8702,GWAS_ID_8703,GWAS_ID_8704,GWAS_ID_8705,GWAS_ID_8706,GWAS_ID_8707,GWAS_ID_8708,GWAS_ID_8709,GWAS_ID_8710,GWAS_ID_8711,GWAS_ID_8712,GWAS_ID_8713,GWAS_ID_8714,GWAS_ID_8715,GWAS_ID_8716,GWAS_ID_8717,GWAS_ID_8718,GWAS_ID_8719,GWAS_ID_8720,GWAS_ID_8721,GWAS_ID_8722,GWAS_ID_8723,GWAS_ID_8724,GWAS_ID_8725,GWAS_ID_8726,GWAS_ID_8727 71441 RMVar_ID_71441 Human_SNP_ID_84031849 m1A Human chr2 - 98731006 98730996 98731006 TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGGAGGGGGCGCGGGGCGGCTGCGCGGAGGGCGCGG TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGG__________GGGCGGCTGCGCGGAGGGCGCGG CCGCGCCCCCT C MGAT4A Ensembl:ENSG00000071073 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98730990..98731107 26863196 MeRIP-seq:(Medium) rs1484625100 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_3638789,Human_RBP_ID_5196394,Human_RBP_ID_8200627,Human_RBP_ID_18422284,Human_RBP_ID_18948076,Human_RBP_ID_22361050 71442 RMVar_ID_71442 Human_SNP_ID_84031854 m1A Human chr2 - 98731006 98731006 98731006 TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGGAGGGGGCGCGGGGCGGCTGCGCGGAGGGCGCGG TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGGGGGGGGCGCGGGGCGGCTGCGCGGAGGGCGCGG T C MGAT4A Ensembl:ENSG00000071073 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98730990..98731107 26863196 MeRIP-seq:(Medium) rs1005991755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638789,Human_RBP_ID_5196394,Human_RBP_ID_8200627,Human_RBP_ID_18422284,Human_RBP_ID_18948076,Human_RBP_ID_22361050 71443 RMVar_ID_71443 Human_SNP_ID_84031855 m1A Human chr2 - 98731006 98731006 98731006 TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGGAGGGGGCGCGGGGCGGCTGCGCGGAGGGCGCGG TCGCGGCGGCAGCGGCGGCGCGCGGGGGCGGGCGGGGGCGCGGGGCGGCTGCGCGGAGGGCGCGG T G MGAT4A Ensembl:ENSG00000071073 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98730990..98731107 26863196 MeRIP-seq:(Medium) rs1005991755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638789,Human_RBP_ID_5196394,Human_RBP_ID_8200627,Human_RBP_ID_18422284,Human_RBP_ID_18948076,Human_RBP_ID_22361050 71444 RMVar_ID_71444 Human_SNP_ID_84053894 m1A Human chr2 - 98822103 98822103 98822103 TCCGGTTAGAAAGGTCGCTGACCGTGCTCCCGAAGGAGGAGAAGTGTCCCCTCGGGACGGCCCCC TCCGGTTAGAAAGGTCGCTGACCGTGCTCCCGCAGGAGGAGAAGTGTCCCCTCGGGACGGCCCCC T G KIAA1211L Ensembl:ENSG00000196872 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:98822056..98822133 26863196 MeRIP-seq:(Medium) rs1387236594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268330 71445 RMVar_ID_71445 Human_SNP_ID_84053971 m1A Human chr2 - 98822269 98822269 98822269 GCCGCCGCGCCCGGCACGAGAGAGCCCTGCCCAGCCGCCCAGGAGCCGGCCCCGAGTGAGGACAG GCCGCCGCGCCCGGCACGAGAGAGCCCTGCCCGGCCGCCCAGGAGCCGGCCCCGAGTGAGGACAG T C KIAA1211L Ensembl:ENSG00000196872 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98822222..98822319 26863196 MeRIP-seq:(Medium) rs1228030321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268330 71446 RMVar_ID_71446 Human_SNP_ID_84054257 m1A Human chr2 - 98822884 98822861 98822885 CCCCCAGGGCCGGCGCCTGAGCCCGAGAGAGAAGCGGAGACGGAGCCCGAGAGAGGAGCGGGGAC CCCCCAGGGCCGGCGCCTGAGCCCGAGAGAG________________________GAGCGGGGAC CCTCTCTCGGGCTCCGTCTCCGCTT C KIAA1211L Ensembl:ENSG00000196872 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98822742..98823026 26863196 MeRIP-seq:(Medium) rs773375745 Functional Loss DEL dbSNP153 32..55 33 - - - RMVar_hsa_circ_268330 71447 RMVar_ID_71447 Human_SNP_ID_84059673 m1A Human chr2 + 98846684 98846684 98846684 GGCCTGCCTCTGTCAGTCCCTCTCCCTGCCCCACAACAAAGCAAGTGCCCTCCCCAGAGCAGGGG GGCCTGCCTCTGTCAGTCCCTCTCCCTGCCCCGCAACAAAGCAAGTGCCCTCCCCAGAGCAGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:98846679..98846797 26863196 MeRIP-seq:(Medium) rs1229479926 Functional Loss SNV dbSNP153 33..33 33 - - - 71448 RMVar_ID_71448 Human_SNP_ID_84129163 m1A Human chr2 - 99141100 99141100 99141100 CTGGGCAGGACGGCGGGCCGAGGAGCCCGGGGAGGGACCCGGAGCTCCAGGTAGAAGCTGCGGAG CTGGGCAGGACGGCGGGCCGAGGAGCCCGGGGGGGGACCCGGAGCTCCAGGTAGAAGCTGCGGAG T C TSGA10 Ensembl:ENSG00000135951 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:99140981..99141139;chr2:99140948..99141132;chr2:99140929..99141132 26863196 MeRIP-seq:(Medium) rs1270523793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830212,Human_RBP_ID_18421854,Human_RBP_ID_22997410 Human_Splice_Rec_279689,Human_Splice_Rec_279909,Human_Splice_Rec_279943 RMVar_hsa_circ_119398,RMVar_hsa_circ_202076 71449 RMVar_ID_71449 Human_SNP_ID_84139386 m1A Human chr2 + 99180897 99180897 99180897 TTGGTAACACACCAGAGCCTGCGGATACCGCGACTCCGAATCTAGTTCTACTGCCCGCTTTAGCA TTGGTAACACACCAGAGCCTGCGGATACCGCGCCTCCGAATCTAGTTCTACTGCCCGCTTTAGCA A C AC092587.1,AC079447.1 Ensembl:ENSG00000273155,Ensembl:ENSG00000241962 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:99180851..99181009 26863196 MeRIP-seq:(Medium) rs764253718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96981,RMVar_hsa_circ_102868,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_202082,RMVar_hsa_circ_202083,RMVar_hsa_circ_202088 71450 RMVar_ID_71450 Human_SNP_ID_84139398 m1A Human chr2 + 99180929 99180929 99180929 ACTCCGAATCTAGTTCTACTGCCCGCTTTAGCACAGTGGCTGCAGCTGTGCTCTGCGGGTCCTGC ACTCCGAATCTAGTTCTACTGCCCGCTTTAGCGCAGTGGCTGCAGCTGTGCTCTGCGGGTCCTGC A G AC092587.1,AC079447.1 Ensembl:ENSG00000273155,Ensembl:ENSG00000241962 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:99180879..99181004 26863196 MeRIP-seq:(Medium) rs1221582709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96981,RMVar_hsa_circ_102868,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_202082,RMVar_hsa_circ_202083,RMVar_hsa_circ_202088 71451 RMVar_ID_71451 Human_SNP_ID_84139401 m1A Human chr2 - 99180933 99180933 99180933 TGAGGCAGGACCCGCAGAGCACAGCTGCAGCCACTGTGCTAAAGCGGGCAGTAGAACTAGATTCG TGAGGCAGGACCCGCAGAGCACAGCTGCAGCCGCTGTGCTAAAGCGGGCAGTAGAACTAGATTCG T C MITD1 Ensembl:ENSG00000158411 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:99180826..99181025 32194978 MeRIP-seq:(Medium) rs1194015275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777268,Human_RBP_ID_4623520,Human_RBP_ID_9384333,Human_RBP_ID_18421857 71452 RMVar_ID_71452 Human_SNP_ID_84176152 m1A Human chr2 + 99337452 99337452 99337452 TCTGTGGAGAGCCGGGTGCGAGCGGCGGCAGCACGAGGGGAAAAGAGCTGAGCGGAGACCAAAGT TCTGTGGAGAGCCGGGTGCGAGCGGCGGCAGCGCGAGGGGAAAAGAGCTGAGCGGAGACCAAAGT A G EIF5B Ensembl:ENSG00000158417 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr2:99337401..99337630;chr2:99337405..99337552 26863196 MeRIP-seq:(Medium) rs1431090732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61506,Human_RBP_ID_4622062,Human_RBP_ID_13999420,Human_RBP_ID_23115046,Human_RBP_ID_24545815,Human_RBP_ID_26338638,Human_RBP_ID_27817415 71453 RMVar_ID_71453 Human_SNP_ID_84176201 m1A Human chr2 + 99337551 99337551 99337551 TAGAGGGGCTGGGGCCACGAGCGCCATTGACAAGCAATGGGGAAGAAACAGAAAAACAAGAGCGA TAGAGGGGCTGGGGCCACGAGCGCCATTGACAGGCAATGGGGAAGAAACAGAAAAACAAGAGCGA A G EIF5B Ensembl:ENSG00000158417 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:99337404..99337600 26863196 MeRIP-seq:(Medium) rs1456960891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9318,Human_RBP_ID_61506,Human_RBP_ID_205332,Human_RBP_ID_243824,Human_RBP_ID_2669824,Human_RBP_ID_5118009,Human_RBP_ID_5471427,Human_RBP_ID_6961532,Human_RBP_ID_9384337,Human_RBP_ID_18166903,Human_RBP_ID_24545817,Human_RBP_ID_26338639,Human_RBP_ID_27817415 Human_Splice_Rec_280297,Human_Splice_Rec_280345 71454 RMVar_ID_71454 Human_SNP_ID_84181846 m1A Human chr2 + 99360386 99360386 99360386 GACTTTGAGTAAGTATATTTTAAATATATTTGATTTTTATTTGTTTTGGTACTGGATTCACTTAA GACTTTGAGTAAGTATATTTTAAATATATTTGGTTTTTATTTGTTTTGGTACTGGATTCACTTAA A G EIF5B Ensembl:ENSG00000158417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:99360384..99360457 26863196 MeRIP-seq:(Medium) rs879176976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64628,RMVar_hsa_circ_352749 71455 RMVar_ID_71455 Human_SNP_ID_84182262 m1A Human chr2 + 99361639 99361639 99361639 AAGGAGCGCGAGAGAAAAAAGCGAGATGAAGAAAAAGCGAAACTGCGGAAGCTGAAAGAAAAAGA AAGGAGCGCGAGAGAAAAAAGCGAGATGAAGAGAAAGCGAAACTGCGGAAGCTGAAAGAAAAAGA A G EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:99361155..99361730 26863196 MeRIP-seq:(Medium) rs747600510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61509,Human_RBP_ID_205336,Human_RBP_ID_1592230,Human_RBP_ID_2669885,Human_RBP_ID_4622111,Human_RBP_ID_9347220,Human_RBP_ID_23115047,Human_RBP_ID_23891496,Human_RBP_ID_24545821 RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_352749,RMVar_hsa_circ_74538 71456 RMVar_ID_71456 Human_SNP_ID_84182275 m1A Human chr2 + 99361666 99361666 99361666 GAAGAAAAAGCGAAACTGCGGAAGCTGAAAGAAAAAGAAGAGTTAGAAACAGGTAAAAAGGATCA GAAGAAAAAGCGAAACTGCGGAAGCTGAAAGAGAAAGAAGAGTTAGAAACAGGTAAAAAGGATCA A G EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:99361290..99361825 26863196 MeRIP-seq:(Medium) rs775794794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61509,Human_RBP_ID_205336,Human_RBP_ID_1592230,Human_RBP_ID_1925852,Human_RBP_ID_2669888,Human_RBP_ID_9347220,Human_RBP_ID_18412774,Human_RBP_ID_23115047,Human_RBP_ID_23891496,Human_RBP_ID_24546108,Human_RBP_ID_26341165,Human_RBP_ID_27818762 RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_352749,RMVar_hsa_circ_74538 71457 RMVar_ID_71457 Human_SNP_ID_84184820 m1A Human chr2 + 99371709 99371709 99371709 ATGCTGGATTGGATGATTGGGAAGCTATGGCCAGTGATGAGGAGACAGAAAAAGGTGAATACCTC ATGCTGGATTGGATGATTGGGAAGCTATGGCCGGTGATGAGGAGACAGAAAAAGGTGAATACCTC A G EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:99371651..99371815 26863196 MeRIP-seq:(Medium) rs1457780064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9320,Human_RBP_ID_918523,Human_RBP_ID_1592238,Human_RBP_ID_6961629,Human_RBP_ID_8528024,Human_RBP_ID_8850992,Human_RBP_ID_9384347,Human_RBP_ID_18544590,Human_RBP_ID_22255311,Human_RBP_ID_22669325,Human_RBP_ID_22997020,Human_RBP_ID_23119300,Human_RBP_ID_23891506,Human_RBP_ID_24545835,Human_RBP_ID_24553106,Human_RBP_ID_26339647,Human_RBP_ID_27817430 Human_Splice_Rec_280314,Human_Splice_Rec_280315,Human_Splice_Rec_280359 Human_miRNA_ID_2155019,Human_miRNA_ID_2158580,Human_miRNA_ID_2392332 RMVar_hsa_circ_53637,RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_352749,RMVar_hsa_circ_71672,RMVar_hsa_circ_109326,RMVar_hsa_circ_75157,RMVar_hsa_circ_68145,RMVar_hsa_circ_285815,RMVar_hsa_circ_367307,RMVar_hsa_circ_202114,RMVar_hsa_circ_110811,RMVar_hsa_circ_62697,RMVar_hsa_circ_68217,RMVar_hsa_circ_202115,RMVar_hsa_circ_202116 71458 RMVar_ID_71458 Human_SNP_ID_84185890 m1A Human chr2 + 99376429 99376426 99376429 GAGGAGGAGGAAGAAGAGGAAGAAGAAGATGAAGAAAGTGAAGAAGAGGAGGAAGAGGAGGGAGA GAGGAGGAGGAAGAAGAGGAAGAAGAAGAT___GAAAGTGAAGAAGAGGAGGAAGAGGAGGGAGA TGAA T EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:99376295..99376571 26863196 MeRIP-seq:(Medium) rs768509532 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_205339,Human_RBP_ID_915727,Human_RBP_ID_1592239,Human_RBP_ID_2669934,Human_RBP_ID_6961656,Human_RBP_ID_8234135,Human_RBP_ID_9347608,Human_RBP_ID_9384348,Human_RBP_ID_18544551,Human_RBP_ID_21982305,Human_RBP_ID_22996857,Human_RBP_ID_23115049,Human_RBP_ID_23119301,Human_RBP_ID_24545836,Human_RBP_ID_24553107,Human_RBP_ID_26339650,Human_RBP_ID_27817431 Human_Splice_Rec_280316,Human_Splice_Rec_280360 RMVar_hsa_circ_53637,RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_71672,RMVar_hsa_circ_109326,RMVar_hsa_circ_75157,RMVar_hsa_circ_68145,RMVar_hsa_circ_367307,RMVar_hsa_circ_110811,RMVar_hsa_circ_62697,RMVar_hsa_circ_68217,RMVar_hsa_circ_202115,RMVar_hsa_circ_202116,RMVar_hsa_circ_324896 71459 RMVar_ID_71459 Human_SNP_ID_84185913 m1A Human chr2 + 99376497 99376497 99376497 TGAAGGCAGTGAAGGTGATGAGGAAGATGAAAAGGTGTCAGATGAGAAGGATTCAGGGAAGACAT TGAAGGCAGTGAAGGTGATGAGGAAGATGAAAGGGTGTCAGATGAGAAGGATTCAGGGAAGACAT A G EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:99376314..99376650 26863196 MeRIP-seq:(Medium) rs776429734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205339,Human_RBP_ID_243086,Human_RBP_ID_915727,Human_RBP_ID_1592240,Human_RBP_ID_1925865,Human_RBP_ID_2675877,Human_RBP_ID_3959418,Human_RBP_ID_6961656,Human_RBP_ID_8234136,Human_RBP_ID_9297434,Human_RBP_ID_9347609,Human_RBP_ID_9384348,Human_RBP_ID_13999890,Human_RBP_ID_17657681,Human_RBP_ID_18193531,Human_RBP_ID_18412648,Human_RBP_ID_18544551,Human_RBP_ID_19028794,Human_RBP_ID_19097994,Human_RBP_ID_20618779,Human_RBP_ID_21982305,Human_RBP_ID_22996780,Human_RBP_ID_23115049,Human_RBP_ID_23119301,Human_RBP_ID_23891512,Human_RBP_ID_24376330,Human_RBP_ID_24545837,Human_RBP_ID_24553107,Human_RBP_ID_26339650,Human_RBP_ID_27817431 RMVar_hsa_circ_53637,RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_71672,RMVar_hsa_circ_109326,RMVar_hsa_circ_75157,RMVar_hsa_circ_68145,RMVar_hsa_circ_367307,RMVar_hsa_circ_110811,RMVar_hsa_circ_62697,RMVar_hsa_circ_68217,RMVar_hsa_circ_202115,RMVar_hsa_circ_202116,RMVar_hsa_circ_324896 71460 RMVar_ID_71460 Human_SNP_ID_84204427 m1A Human chr2 + 99449486 99449486 99449486 ATTGACCTCCATGCAACATCATTAGTTTTCTCAATTCCTCAGCGGAAGGATCTGCAAAATTTATA ATTGACCTCCATGCAACATCATTAGTTTTCTCGATTCCTCAGCGGAAGGATCTGCAAAATTTATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:99449439..99451380 26863196 MeRIP-seq:(Medium) rs1245762889 Functional Loss SNV dbSNP153 33..33 33 - - - 71461 RMVar_ID_71461 Human_SNP_ID_84215085 m1A Human chr2 - 99490126 99490126 99490126 CGAGGCTGGGGTCGCCCCGGGCCGGGGGGAGCAGAGCGCGTGCGCCGCGCGGCTGTGAGCGCGAG CGAGGCTGGGGTCGCCCCGGGCCGGGGGGAGCGGAGCGCGTGCGCCGCGCGGCTGTGAGCGCGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:99490084..99490173 26863196 MeRIP-seq:(Medium) rs1445281339 Functional Loss SNV dbSNP153 33..33 33 - - - 71462 RMVar_ID_71462 Human_SNP_ID_84433781 m1A Human chr2 + 100406613 100406613 100406613 GGGTCTTTAAAGGTCAACGTGATGAACTTGCTAGCCACCATGAACATGAAAATCACCCAAAAGCA GGGTCTTTAAAGGTCAACGTGATGAACTTGCTGGCCACCATGAACATGAAAATCACCCAAAAGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:100402642..100407677 32194978 MeRIP-seq:(Medium) rs1324974796 Functional Loss SNV dbSNP153 33..33 33 - - - 71463 RMVar_ID_71463 Human_SNP_ID_84473574 m1A Human chr2 + 100563066 100563062 100563067 CACAGCTGGTTTGAGCAACTGAACTGGAAACAAGATGCAGGTGAGCTAGGACGGGTCTCGGGTCT CACAGCTGGTTTGAGCAACTGAACTGGAA_____ATGCAGGTGAGCTAGGACGGGTCTCGGGTCT AACAAG A PDCL3 Ensembl:ENSG00000115539 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100562951..100563319 26863196 MeRIP-seq:(Medium) rs747094564 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_1576249,Human_RBP_ID_4623526,Human_RBP_ID_19101201,Human_RBP_ID_26339671 Human_Splice_Rec_281185 71464 RMVar_ID_71464 Human_SNP_ID_84473575 m1A Human chr2 + 100563063 100563063 100563063 CGGCACAGCTGGTTTGAGCAACTGAACTGGAAACAAGATGCAGGTGAGCTAGGACGGGTCTCGGG CGGCACAGCTGGTTTGAGCAACTGAACTGGAAGCAAGATGCAGGTGAGCTAGGACGGGTCTCGGG A G PDCL3 Ensembl:ENSG00000115539 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:100562951..100563418 26863196 MeRIP-seq:(Medium) rs372336455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1576249,Human_RBP_ID_4623526,Human_RBP_ID_19101201,Human_RBP_ID_26339671,Human_RBP_ID_27818787 Human_Splice_Rec_281185 71465 RMVar_ID_71465 Human_SNP_ID_84473580 m1A Human chr2 + 100563066 100563066 100563066 CACAGCTGGTTTGAGCAACTGAACTGGAAACAAGATGCAGGTGAGCTAGGACGGGTCTCGGGTCT CACAGCTGGTTTGAGCAACTGAACTGGAAACAGGATGCAGGTGAGCTAGGACGGGTCTCGGGTCT A G PDCL3 Ensembl:ENSG00000115539 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100562951..100563319 26863196 MeRIP-seq:(Medium) rs974253366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1576249,Human_RBP_ID_4623526,Human_RBP_ID_19101201,Human_RBP_ID_26339671 Human_Splice_Rec_281185 71466 RMVar_ID_71466 Human_SNP_ID_84474897 m1A Human chr2 + 100567508 100567508 100567508 CTCAGAGAGGGCCTCACTGAGATGACATTTGCATGGACCTGAAGGAGGTGAAGCTGGCATTTGGG CTCAGAGAGGGCCTCACTGAGATGACATTTGCGTGGACCTGAAGGAGGTGAAGCTGGCATTTGGG A G PDCL3 Ensembl:ENSG00000115539 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:100567457..100567529 26863196 MeRIP-seq:(Medium) rs1483498731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326252,RMVar_hsa_circ_356589 71467 RMVar_ID_71467 Human_SNP_ID_84475313 m1A Human chr2 - 100569007 100569007 100569007 CCTCTGGGTGGCGCTTACCTGTACATTTCAATAGCACGTTCATCCTCCTCATTAAACTCGTCTTC CCTCTGGGTGGCGCTTACCTGTACATTTCAATGGCACGTTCATCCTCCTCATTAAACTCGTCTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100568951..100569614 26863196 MeRIP-seq:(Medium) rs774029641 Functional Loss SNV dbSNP153 33..33 33 - - - 71468 RMVar_ID_71468 Human_SNP_ID_84539806 m1A Human chr2 + 100820277 100820269 100820278 CCGCGGCGGCGGCGGCGGCGGCGGCAGCAGCTAGAGCAGCGCCTCCCGCCGCCGCCCGGGAGGAG CCGCGGCGGCGGCGGCGGCGGCGGC_________AGCAGCGCCTCCCGCCGCCGCCCGGGAGGAG CAGCAGCTAG C NPAS2 Ensembl:ENSG00000170485 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:100820197..100820316 26863410 MeRIP-seq:(Medium) rs1407701740 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_4622590 71469 RMVar_ID_71469 Human_SNP_ID_84539858 m1A Human chr2 + 100820413 100820413 100820413 CCGGCCCCGCGGGGCCGCTCCGGCCCGCTCCGAGGTAAGGGGCCGCGCCTAGGGGCGCGGGGGAC CCGGCCCCGCGGGGCCGCTCCGGCCCGCTCCGGGGTAAGGGGCCGCGCCTAGGGGCGCGGGGGAC A G NPAS2 Ensembl:ENSG00000170485 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100820128..100820629 26863196 MeRIP-seq:(Medium) rs1315893031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624590 Human_Splice_Rec_281229 71470 RMVar_ID_71470 Human_SNP_ID_84568406 m1A Human chr2 + 100940862 100940862 100940862 CAGAGTGTGGGGCTCAGAAAGGGAGAATGAGGAGCTGAGAGGTGGTGGTCGCTCCTCGAGGAAGA CAGAGTGTGGGGCTCAGAAAGGGAGAATGAGGTGCTGAGAGGTGGTGGTCGCTCCTCGAGGAAGA A T NPAS2 Ensembl:ENSG00000170485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100940856..100940939 26863196 MeRIP-seq:(Medium) rs1256685432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97379,RMVar_hsa_circ_202182,RMVar_hsa_circ_343700,RMVar_hsa_circ_43222,RMVar_hsa_circ_96982,RMVar_hsa_circ_64712,RMVar_hsa_circ_202184,RMVar_hsa_circ_267166,RMVar_hsa_circ_117312,RMVar_hsa_circ_79884,RMVar_hsa_circ_202189,RMVar_hsa_circ_202186,RMVar_hsa_circ_202187,RMVar_hsa_circ_282538,RMVar_hsa_circ_310949,RMVar_hsa_circ_325440,RMVar_hsa_circ_275559,RMVar_hsa_circ_202190,RMVar_hsa_circ_202192,RMVar_hsa_circ_202191 71471 RMVar_ID_71471 Human_SNP_ID_84569869 m1A Human chr2 - 100946998 100946998 100946998 CCCTGGGGACCACAGATGAATACATGTCCTGAACATCGGCATTCTTTCCCACCCATATCATCTCC CCCTGGGGACCACAGATGAATACATGTCCTGAGCATCGGCATTCTTTCCCACCCATATCATCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100946926..100947052 26863196 MeRIP-seq:(Medium) rs933515283 Functional Loss SNV dbSNP153 33..33 33 - - - 71472 RMVar_ID_71472 Human_SNP_ID_84580302 m1A Human chr2 - 100988784 100988784 100988784 CAGGGAGACCTGGAGGAGCAATGGGGGCCTGGAGGAGCAGGGAGACCTGGAGGAGCAGTGGGGGC CAGGGAGACCTGGAGGAGCAATGGGGGCCTGGGGGAGCAGGGAGACCTGGAGGAGCAGTGGGGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:100988761..100988918 26863196 MeRIP-seq:(Medium) rs1206780838 Functional Loss SNV dbSNP153 33..33 33 - - - 71473 RMVar_ID_71473 Human_SNP_ID_84583694 m1A Human chr2 + 101002315 101002315 101002315 CGCGCTCTTCCTTTCCAACTTGGACGCTGCAGAGTGAGTATGGGTGGCGGAGTCTGGGCTCCTGG CGCGCTCTTCCTTTCCAACTTGGACGCTGCAGGGTGAGTATGGGTGGCGGAGTCTGGGCTCCTGG A G RPL31 Ensembl:ENSG00000071082 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:101002276..101002373;chr2:101002276..101002325 26863196 MeRIP-seq:(Medium) rs1464228079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774608,Human_RBP_ID_827584,Human_RBP_ID_916508,Human_RBP_ID_4623527,Human_RBP_ID_5118336,Human_RBP_ID_5379728,Human_RBP_ID_9330615,Human_RBP_ID_9384380,Human_RBP_ID_17279832,Human_RBP_ID_17392759,Human_RBP_ID_18193372,Human_RBP_ID_18743290,Human_RBP_ID_19098017,Human_RBP_ID_21893756,Human_RBP_ID_23257904,Human_RBP_ID_26787103,Human_RBP_ID_26818812 Human_Splice_Rec_281391,Human_Splice_Rec_281395,Human_Splice_Rec_281403,Human_Splice_Rec_281411,Human_Splice_Rec_281423,Human_Splice_Rec_281431,Human_Splice_Rec_281439 RMVar_hsa_circ_114633,RMVar_hsa_circ_202205 71474 RMVar_ID_71474 Human_SNP_ID_84583831 m1A Human chr2 + 101002736 101002736 101002736 GGCTCCCGCAAAGAAGGGTGGCGAGAAGAAAAAGGGCCGTTCTGCCATCAACGAAGTGGTAACCC GGCTCCCGCAAAGAAGGGTGGCGAGAAGAAAAGGGGCCGTTCTGCCATCAACGAAGTGGTAACCC A G RPL31 Ensembl:ENSG00000071082 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:101002263..101004225 26863196 MeRIP-seq:(Medium) rs1434799404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530685,Human_RBP_ID_1133498,Human_RBP_ID_1576259,Human_RBP_ID_1894459,Human_RBP_ID_3590470,Human_RBP_ID_4575800,Human_RBP_ID_8497695,Human_RBP_ID_9091737,Human_RBP_ID_9330616,Human_RBP_ID_9387139,Human_RBP_ID_9933995,Human_RBP_ID_14002002,Human_RBP_ID_17279833,Human_RBP_ID_17392762,Human_RBP_ID_18743291,Human_RBP_ID_20616780,Human_RBP_ID_23815150,Human_RBP_ID_26339676,Human_RBP_ID_26487813,Human_RBP_ID_26770379,Human_RBP_ID_26818814,Human_RBP_ID_26998476,Human_RBP_ID_27280999 Human_Splice_Rec_281392,Human_Splice_Rec_281393,Human_Splice_Rec_281396,Human_Splice_Rec_281397,Human_Splice_Rec_281404,Human_Splice_Rec_281405,Human_Splice_Rec_281412,Human_Splice_Rec_281413,Human_Splice_Rec_281417,Human_Splice_Rec_281424,Human_Splice_Rec_281425,Human_Splice_Rec_281432,Human_Splice_Rec_281433,Human_Splice_Rec_281440,Human_Splice_Rec_281441,Human_Splice_Rec_281445,Human_Splice_Rec_281449,Human_Splice_Rec_281451 RMVar_hsa_circ_63143,RMVar_hsa_circ_114633,RMVar_hsa_circ_202205 71475 RMVar_ID_71475 Human_SNP_ID_84583834 m1A Human chr2 - 101002743 101002743 101002743 TATTCTCGGGTTACCACTTCGTTGATGGCAGAACGGCCCTTTTTCTTCTCGCCACCCTTCTTTGC TATTCTCGGGTTACCACTTCGTTGATGGCAGAGCGGCCCTTTTTCTTCTCGCCACCCTTCTTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:101002276..101004225 26863196 MeRIP-seq:(Medium) rs1558957088 Functional Loss SNV dbSNP153 33..33 33 - - - 71476 RMVar_ID_71476 Human_SNP_ID_84583849 m1A Human chr2 - 101002803 101002803 101002803 ACCCAGGGCGGCTAGAGGGATACTCACACTCCATGGATGCGCTTGTGAATGTTGATGGTGTATTC ACCCAGGGCGGCTAGAGGGATACTCACACTCCGTGGATGCGCTTGTGAATGTTGATGGTGTATTC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:101002694..101002850 26863410 MeRIP-seq:(Medium) rs940541305 Functional Loss SNV dbSNP153 33..33 33 - - - 71477 RMVar_ID_71477 Human_SNP_ID_84584465 m1A Human chr2 + 101004813 101004813 101004813 CATGGGGCTGCTCCCTCAACAAAAAATTGCCTAGCTCAGATGTTAGTTCTCATGTTGGGGGACCC CATGGGGCTGCTCCCTCAACAAAAAATTGCCTGGCTCAGATGTTAGTTCTCATGTTGGGGGACCC A G RPL31 Ensembl:ENSG00000071082 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101004810..101005248 26863196 MeRIP-seq:(Medium) rs1273773049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8497705,Human_RBP_ID_13559388 RMVar_hsa_circ_63143,RMVar_hsa_circ_114633,RMVar_hsa_circ_202205,RMVar_hsa_circ_202206,RMVar_hsa_circ_98723 71478 RMVar_ID_71478 Human_SNP_ID_84584828 m1A Human chr2 + 101006009 101006009 101006009 CCGTGTGCGGCTGTCCAGAAAACGTAATGAGGATGAAGATTCACCAAATAAGCTATATACTTTGG CCGTGTGCGGCTGTCCAGAAAACGTAATGAGGGTGAAGATTCACCAAATAAGCTATATACTTTGG A G RPL31 Ensembl:ENSG00000071082 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:101005912..101006026 26863196 MeRIP-seq:(Medium) rs1065720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530699,Human_RBP_ID_1576269,Human_RBP_ID_1894468,Human_RBP_ID_3590475,Human_RBP_ID_8497707,Human_RBP_ID_9091741,Human_RBP_ID_13559441,Human_RBP_ID_23815166,Human_RBP_ID_26998485 Human_Splice_Rec_281400,Human_Splice_Rec_281401,Human_Splice_Rec_281408,Human_Splice_Rec_281409,Human_Splice_Rec_281416,Human_Splice_Rec_281420,Human_Splice_Rec_281421,Human_Splice_Rec_281428,Human_Splice_Rec_281429,Human_Splice_Rec_281436,Human_Splice_Rec_281437,Human_Splice_Rec_281444,Human_Splice_Rec_281448,Human_Splice_Rec_281454,Human_Splice_Rec_281455 RMVar_hsa_circ_63143,RMVar_hsa_circ_114633,RMVar_hsa_circ_202205,RMVar_hsa_circ_202208,RMVar_hsa_circ_118770,RMVar_hsa_circ_202206,RMVar_hsa_circ_98723,RMVar_hsa_circ_121270,RMVar_hsa_circ_89706,RMVar_hsa_circ_202209,RMVar_hsa_circ_202207 71479 RMVar_ID_71479 Human_SNP_ID_84584941 m1A Human chr2 + 101006354 101006354 101006354 TGGAAATTGACTGTTACTTCCTTTACAGATCTACAGACAGTCAATGTGGATGAGAACTAATCGCT TGGAAATTGACTGTTACTTCCTTTACAGATCTGCAGACAGTCAATGTGGATGAGAACTAATCGCT A G RPL31 Ensembl:ENSG00000071082 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:101006351..101006425 32194978 MeRIP-seq:(Medium) rs750021597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326,Human_RBP_ID_56395,Human_RBP_ID_530709,Human_RBP_ID_920674,Human_RBP_ID_1576276,Human_RBP_ID_1894474,Human_RBP_ID_2574549,Human_RBP_ID_3590481,Human_RBP_ID_8497715,Human_RBP_ID_9091745,Human_RBP_ID_9384388,Human_RBP_ID_13559454,Human_RBP_ID_17277869,Human_RBP_ID_17388409,Human_RBP_ID_17509733,Human_RBP_ID_18308521,Human_RBP_ID_18743304,Human_RBP_ID_19101230,Human_RBP_ID_20615684,Human_RBP_ID_21908749,Human_RBP_ID_22076520,Human_RBP_ID_22547486,Human_RBP_ID_22705863,Human_RBP_ID_22742988,Human_RBP_ID_22980162,Human_RBP_ID_23211675,Human_RBP_ID_23815169,Human_RBP_ID_25450322,Human_RBP_ID_26818820,Human_RBP_ID_26998488,Human_RBP_ID_27817450 Human_Splice_Rec_281410,Human_Splice_Rec_281422 RMVar_hsa_circ_114633,RMVar_hsa_circ_202205,RMVar_hsa_circ_202208,RMVar_hsa_circ_202206,RMVar_hsa_circ_98723,RMVar_hsa_circ_121270,RMVar_hsa_circ_89706,RMVar_hsa_circ_202209,RMVar_hsa_circ_89530,RMVar_hsa_circ_202210 71480 RMVar_ID_71480 Human_SNP_ID_84618659 m1A Human chr2 + 101139638 101139638 101139638 TCCTCCTCTACAGGCCTTTCTAGACAAGTCCCAGGTATCCCACACTTAACTTGTCCAAAACAGAC TCCTCCTCTACAGGCCTTTCTAGACAAGTCCCCGGTATCCCACACTTAACTTGTCCAAAACAGAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101139637..101139800 26863196 MeRIP-seq:(Medium) rs1315769691 Functional Loss SNV dbSNP153 33..33 33 - - - 71481 RMVar_ID_71481 Human_SNP_ID_84621012 m1A Human chr2 + 101149845 101149845 101149845 CCTCCCCCAAAGCTCAAAACAGCTCCTGGAGCAGGCCCACGTGCTGCCCAAGTTGCCCAAGTTGA CCTCCCCCAAAGCTCAAAACAGCTCCTGGAGCCGGCCCACGTGCTGCCCAAGTTGCCCAAGTTGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101149839..101150049 26863196 MeRIP-seq:(Medium) rs1363298899 Functional Loss SNV dbSNP153 33..33 33 - - - 71482 RMVar_ID_71482 Human_SNP_ID_84621222 m1A Human chr2 + 101150688 101150688 101150688 GCTGCGCCCCGCGCGCATCGCCGCGCGCCCCCAGCCACGACACCACCTGGAGCCTCCGGCGCCTC GCTGCGCCCCGCGCGCATCGCCGCGCGCCCCCGGCCACGACACCACCTGGAGCCTCCGGCGCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101150678..101150831 26863196 MeRIP-seq:(Medium) rs904833234 Functional Loss SNV dbSNP153 33..33 33 - - - 71483 RMVar_ID_71483 Human_SNP_ID_84645539 m1A Human chr2 - 101253046 101253046 101253046 GCCGGAGCCCCCGAAGCCGCTCCTGGACGCCGACCCTGCCGCTTCCCGGGACCCTCTTTGCTCCG GCCGGAGCCCCCGAAGCCGCTCCTGGACGCCGCCCCTGCCGCTTCCCGGGACCCTCTTTGCTCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:101252901..101253175 26863196 MeRIP-seq:(Medium) rs913464922 Functional Loss SNV dbSNP153 33..33 33 - - - 71484 RMVar_ID_71484 Human_SNP_ID_84645720 m1A Human chr2 + 101253416 101253416 101253416 GGCCGCCAACCCCTTCGCCGCCAGCTTCGCGCACCTGCTCAACCCCGCGCCGCCCGCCCGCGGCG GGCCGCCAACCCCTTCGCCGCCAGCTTCGCGCGCCTGCTCAACCCCGCGCCGCCCGCCCGCGGCG A G CNOT11 Ensembl:ENSG00000158435 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:101253294..101257871 26863196 MeRIP-seq:(Medium) rs931424871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_281567 Human_miRNA_ID_2249885 RMVar_hsa_circ_18397,RMVar_hsa_circ_202229,RMVar_hsa_circ_123572 71485 RMVar_ID_71485 Human_SNP_ID_84659184 m1A Human chr2 - 101308569 101308543 101308569 CAGCGGTGCTGCCATGGCGTGGCGGCGGCGCGAAGCCAGCGTCGGGGCTCGCGGCGTGTTGGCTC CAGCGGTGCTGCCATGGCGTGGCGGCGGCGCG__________________________TTGGCTC ACACGCCGCGAGCCCCGACGCTGGCTT A RNF149 Ensembl:ENSG00000163162 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:101308482..101308622 26863410 MeRIP-seq:(Medium) rs763477444 Functional Loss DEL dbSNP153 33..58 33 - - - Human_RBP_ID_4624600,Human_RBP_ID_22077213,Human_RBP_ID_22450516 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 71486 RMVar_ID_71486 Human_SNP_ID_84659202 m1A Human chr2 - 101308569 101308569 101308569 CAGCGGTGCTGCCATGGCGTGGCGGCGGCGCGAAGCCAGCGTCGGGGCTCGCGGCGTGTTGGCTC CAGCGGTGCTGCCATGGCGTGGCGGCGGCGCGGAGCCAGCGTCGGGGCTCGCGGCGTGTTGGCTC T C RNF149 Ensembl:ENSG00000163162 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:101308482..101308622 26863410 MeRIP-seq:(Medium) rs1413131596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624600,Human_RBP_ID_22077213,Human_RBP_ID_22450516 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 71487 RMVar_ID_71487 Human_SNP_ID_84659219 m1A Human chr2 - 101308588 101308588 101308588 TGACTCCCCCTAGTCAGCTCAGCGGTGCTGCCATGGCGTGGCGGCGGCGCGAAGCCAGCGTCGGG TGACTCCCCCTAGTCAGCTCAGCGGTGCTGCCGTGGCGTGGCGGCGGCGCGAAGCCAGCGTCGGG T C RNF149 Ensembl:ENSG00000163162 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101308539..101308632 26863196 MeRIP-seq:(Medium) rs781096428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1296575,Human_RBP_ID_4624600,Human_RBP_ID_18422763,Human_RBP_ID_22077213,Human_RBP_ID_22451552 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 71488 RMVar_ID_71488 Human_SNP_ID_84756494 m1A Human chr2 + 101697804 101697804 101697804 GGCGCGGGCGCCGGGGCCTGAGGCGGCGGGCGACGCCCGGGGGCCTGACGGCCGGCCCCGCGCCA GGCGCGGGCGCCGGGGCCTGAGGCGGCGGGCGCCGCCCGGGGGCCTGACGGCCGGCCCCGCGCCA A C MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:101697701..101698017 26863410 MeRIP-seq:(Medium) rs1330033771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243387,Human_RBP_ID_4622594,Human_RBP_ID_8851476,Human_RBP_ID_9296771,Human_RBP_ID_9331132,Human_RBP_ID_9384399 71489 RMVar_ID_71489 Human_SNP_ID_84756520 m1A Human chr2 + 101697895 101697895 101697895 GCTCCGTCCGCCCTCCGCGCGGCCCGGCCGGCAGAGAGCCCCGAGCGGCCCGAGAGCGCAGCCGA GCTCCGTCCGCCCTCCGCGCGGCCCGGCCGGCTGAGAGCCCCGAGCGGCCCGAGAGCGCAGCCGA A T MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:101697702..101698031 26863196 MeRIP-seq:(Medium) rs1043614940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622595,Human_RBP_ID_8851477,Human_RBP_ID_8942609,Human_RBP_ID_9296773,Human_RBP_ID_9384400,Human_RBP_ID_22533599 71490 RMVar_ID_71490 Human_SNP_ID_84756574 m1A Human chr2 + 101698031 101698031 101698031 TCGGCGGCCTGGTCTGCGGCTGAGATACACAGAGCGACAGAGACATTTATTGTTATTTGTTTTTT TCGGCGGCCTGGTCTGCGGCTGAGATACACAGGGCGACAGAGACATTTATTGTTATTTGTTTTTT A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:101697734..101698150 26863196 MeRIP-seq:(Medium) rs557458944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625509,Human_RBP_ID_18442305 71491 RMVar_ID_71491 Human_SNP_ID_84756576 m1A Human chr2 + 101698037 101698036 101698038 GCCTGGTCTGCGGCTGAGATACACAGAGCGACAGAGACATTTATTGTTATTTGTTTTTTGGTGGC GCCTGGTCTGCGGCTGAGATACACAGAGCGAC__AGACATTTATTGTTATTTGTTTTTTGGTGGC CAG C MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101697786..101698086 32194978 MeRIP-seq:(Medium) rs751323380 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4625509 71492 RMVar_ID_71492 Human_SNP_ID_84789010 m1A Human chr2 - 101824002 101824002 101824002 CCTGGAGGGCTCTTTTTGATGAAAGCACCATAATATGTTGCAATGTTTCTGTGATGAGAGTATTT CCTGGAGGGCTCTTTTTGATGAAAGCACCATATTATGTTGCAATGTTTCTGTGATGAGAGTATTT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:101823951..101824052 32194978 MeRIP-seq:(Medium) rs55856263 Functional Loss SNV dbSNP153 33..33 33 - - - 71493 RMVar_ID_71493 Human_SNP_ID_84789011 m1A Human chr2 - 101824002 101824002 101824002 CCTGGAGGGCTCTTTTTGATGAAAGCACCATAATATGTTGCAATGTTTCTGTGATGAGAGTATTT CCTGGAGGGCTCTTTTTGATGAAAGCACCATAGTATGTTGCAATGTTTCTGTGATGAGAGTATTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:101823951..101824052 32194978 MeRIP-seq:(Medium) rs55856263 Functional Loss SNV dbSNP153 33..33 33 - - - 71494 RMVar_ID_71494 Human_SNP_ID_84796483 m1A Human chr2 - 101856000 101856000 101856000 CTCCTTCGCTGTTCACGTTCCTGCTGCCTTCTAGCTTCCCGCTCTCTCCTTTGTTGCTACGTAAG CTCCTTCGCTGTTCACGTTCCTGCTGCCTTCTTGCTTCCCGCTCTCTCCTTTGTTGCTACGTAAG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr2:101855976..101856144;chr2:101839974..101859825 26863196 MeRIP-seq:(Medium) rs996503289 Functional Loss SNV dbSNP153 33..33 33 - - - 71495 RMVar_ID_71495 Human_SNP_ID_84796488 m1A Human chr2 + 101856020 101856020 101856020 AGAGCGGGAAGCTAGAAGGCAGCAGGAACGTGAACAGCGAAGGAGAGAACAAGAAGAAAAGAGGC AGAGCGGGAAGCTAGAAGGCAGCAGGAACGTGCACAGCGAAGGAGAGAACAAGAAGAAAAGAGGC A C MAP4K4 Ensembl:ENSG00000071054 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:101855924..101856150 26863196 MeRIP-seq:(Medium) rs1559204080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56388,Human_RBP_ID_264389,Human_RBP_ID_2575264,Human_RBP_ID_9347619,Human_RBP_ID_9384442,Human_RBP_ID_18412788,Human_RBP_ID_22742997,Human_RBP_ID_22997027,Human_RBP_ID_23119314,Human_RBP_ID_24546128,Human_RBP_ID_24553113,Human_RBP_ID_26339690,Human_RBP_ID_27817462 Human_Splice_Rec_281790,Human_Splice_Rec_281850,Human_Splice_Rec_281906,Human_Splice_Rec_281964,Human_Splice_Rec_282024,Human_Splice_Rec_282082,Human_Splice_Rec_282130,Human_Splice_Rec_282188,Human_Splice_Rec_282240,Human_Splice_Rec_282294,Human_Splice_Rec_282344,Human_Splice_Rec_282398,Human_Splice_Rec_282458,Human_Splice_Rec_282468 RMVar_hsa_circ_3582,RMVar_hsa_circ_70658,RMVar_hsa_circ_13472,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_116064,RMVar_hsa_circ_202264,RMVar_hsa_circ_21524,RMVar_hsa_circ_65403,RMVar_hsa_circ_315560,RMVar_hsa_circ_70966,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_342280,RMVar_hsa_circ_53472,RMVar_hsa_circ_202265 71496 RMVar_ID_71496 Human_SNP_ID_84796492 m1A Human chr2 + 101856045 101856045 101856045 GAACGTGAACAGCGAAGGAGAGAACAAGAAGAAAAGAGGCGTCTAGAGGAGTTGGAGAGAAGGCG GAACGTGAACAGCGAAGGAGAGAACAAGAAGAGAAGAGGCGTCTAGAGGAGTTGGAGAGAAGGCG A G MAP4K4 Ensembl:ENSG00000071054 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:101855919..101856150 26863196 MeRIP-seq:(Medium) rs1392325354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56388,Human_RBP_ID_264389,Human_RBP_ID_9347619,Human_RBP_ID_9384443,Human_RBP_ID_17509734,Human_RBP_ID_18412652,Human_RBP_ID_22742997,Human_RBP_ID_22997027,Human_RBP_ID_23119314,Human_RBP_ID_24545841,Human_RBP_ID_26339690,Human_RBP_ID_27817463 Human_Splice_Rec_281790,Human_Splice_Rec_281791,Human_Splice_Rec_281850,Human_Splice_Rec_281851,Human_Splice_Rec_281906,Human_Splice_Rec_281907,Human_Splice_Rec_281964,Human_Splice_Rec_281965,Human_Splice_Rec_282024,Human_Splice_Rec_282025,Human_Splice_Rec_282082,Human_Splice_Rec_282083,Human_Splice_Rec_282130,Human_Splice_Rec_282131,Human_Splice_Rec_282188,Human_Splice_Rec_282189,Human_Splice_Rec_282240,Human_Splice_Rec_282241,Human_Splice_Rec_282294,Human_Splice_Rec_282295,Human_Splice_Rec_282344,Human_Splice_Rec_282345,Human_Splice_Rec_282398,Human_Splice_Rec_282399,Human_Splice_Rec_282458,Human_Splice_Rec_282459,Human_Splice_Rec_282468,Human_Splice_Rec_282469,Human_Splice_Rec_282505 RMVar_hsa_circ_3582,RMVar_hsa_circ_70658,RMVar_hsa_circ_13472,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_116064,RMVar_hsa_circ_202264,RMVar_hsa_circ_21524,RMVar_hsa_circ_65403,RMVar_hsa_circ_315560,RMVar_hsa_circ_70966,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_342280,RMVar_hsa_circ_53472,RMVar_hsa_circ_202265 71497 RMVar_ID_71497 Human_SNP_ID_84797427 m1A Human chr2 + 101859795 101859795 101859795 CACTCGCAGCAGCCGCCACCACCGCAGCAGGAAAGGAGCAAGCCAAGCTTCCATGCTCCCGAGCC CACTCGCAGCAGCCGCCACCACCGCAGCAGGAGAGGAGCAAGCCAAGCTTCCATGCTCCCGAGCC A G MAP4K4 Ensembl:ENSG00000071054 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101844268..101859899 32194978 MeRIP-seq:(Medium) rs774052467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3959436,Human_RBP_ID_9297448,Human_RBP_ID_9384458,Human_RBP_ID_27817465 Human_Splice_Rec_281794,Human_Splice_Rec_281795,Human_Splice_Rec_281854,Human_Splice_Rec_281855,Human_Splice_Rec_281910,Human_Splice_Rec_281911,Human_Splice_Rec_281968,Human_Splice_Rec_281969,Human_Splice_Rec_282028,Human_Splice_Rec_282029,Human_Splice_Rec_282086,Human_Splice_Rec_282087,Human_Splice_Rec_282135,Human_Splice_Rec_282193,Human_Splice_Rec_282245,Human_Splice_Rec_282299,Human_Splice_Rec_282349,Human_Splice_Rec_282402,Human_Splice_Rec_282403,Human_Splice_Rec_282462,Human_Splice_Rec_282473,Human_Splice_Rec_282509 RMVar_hsa_circ_3582,RMVar_hsa_circ_70658,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_116064,RMVar_hsa_circ_202264,RMVar_hsa_circ_21524,RMVar_hsa_circ_315560,RMVar_hsa_circ_9734,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_342280,RMVar_hsa_circ_53472,RMVar_hsa_circ_22934,RMVar_hsa_circ_307246,RMVar_hsa_circ_202265,RMVar_hsa_circ_43332,RMVar_hsa_circ_39473,RMVar_hsa_circ_202266 71498 RMVar_ID_71498 Human_SNP_ID_84799993 m1A Human chr2 + 101869633 101869633 101869633 CTTTTCTGTCCTTTGCTTTAGGATCTGACCGCACTGGCCAAAGAGCTTCGAGCAGTGGAAGATGT CTTTTCTGTCCTTTGCTTTAGGATCTGACCGCGCTGGCCAAAGAGCTTCGAGCAGTGGAAGATGT A G MAP4K4 Ensembl:ENSG00000071054 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101869626..101869675 32194978 MeRIP-seq:(Medium) rs1350842517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921493,Human_RBP_ID_2575274,Human_RBP_ID_8851487,Human_RBP_ID_9297451,Human_RBP_ID_18743455,Human_RBP_ID_22667677,Human_RBP_ID_26338664 Human_Splice_Rec_281804,Human_Splice_Rec_281862,Human_Splice_Rec_281920,Human_Splice_Rec_281978,Human_Splice_Rec_282038,Human_Splice_Rec_282094,Human_Splice_Rec_282144,Human_Splice_Rec_282204,Human_Splice_Rec_282308,Human_Splice_Rec_282356,Human_Splice_Rec_282412,Human_Splice_Rec_282484,Human_Splice_Rec_282516,Human_Splice_Rec_282520 RMVar_hsa_circ_70658,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_22934,RMVar_hsa_circ_43332,RMVar_hsa_circ_57858,RMVar_hsa_circ_365176,RMVar_hsa_circ_378941 71499 RMVar_ID_71499 Human_SNP_ID_84800217 m1A Human chr2 - 101870358 101870358 101870358 TTGGATGGGGTCATGGCCGGCTCACTTTCTACATCATCATGGACAATCATGGTTTTCACAGATTC TTGGATGGGGTCATGGCCGGCTCACTTTCTACGTCATCATGGACAATCATGGTTTTCACAGATTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101870308..101870409 32194978 MeRIP-seq:(Medium) rs1190933741 Functional Loss SNV dbSNP153 33..33 33 - - - 71500 RMVar_ID_71500 Human_SNP_ID_84804884 m1A Human chr2 - 101888871 101888871 101888871 TTTGAGCCCTTTTGTGCATGAACACACCATCCAAGTGACCAGTTTCCACAGATCGGATCTCTATG TTTGAGCCCTTTTGTGCATGAACACACCATCCCAGTGACCAGTTTCCACAGATCGGATCTCTATG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101887912..101888871 32194978 MeRIP-seq:(Medium) rs1166592141 Functional Loss SNV dbSNP153 33..33 33 - - - 71501 RMVar_ID_71501 Human_SNP_ID_85020726 m1A Human chr2 + 102736767 102736767 102736767 GCTCCTGTTTCCGCTCTGCGGTCTCCGAGACCAGCCTCGGGGCCGAGTTCATGTCCCAGTGACCC GCTCCTGTTTCCGCTCTGCGGTCTCCGAGACCCGCCTCGGGGCCGAGTTCATGTCCCAGTGACCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:102736724..102736827 26863196 MeRIP-seq:(Medium) rs1308161324 Functional Loss SNV dbSNP153 33..33 33 - - - 71502 RMVar_ID_71502 Human_SNP_ID_85020820 m1A Human chr2 + 102736851 102736851 102736851 CGGCCGGGGGTCGGACGCAGCAGCAGCCGCGGACCTACCCCGGGAGCCCAGCCCCGCCCCGAGCG CGGCCGGGGGTCGGACGCAGCAGCAGCCGCGGCCCTACCCCGGGAGCCCAGCCCCGCCCCGAGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:102736714..102736874 26863196 MeRIP-seq:(Medium) rs751746726 Functional Loss SNV dbSNP153 33..33 33 - - - 71503 RMVar_ID_71503 Human_SNP_ID_85020821 m1A Human chr2 + 102736851 102736851 102736851 CGGCCGGGGGTCGGACGCAGCAGCAGCCGCGGACCTACCCCGGGAGCCCAGCCCCGCCCCGAGCG CGGCCGGGGGTCGGACGCAGCAGCAGCCGCGGGCCTACCCCGGGAGCCCAGCCCCGCCCCGAGCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:102736714..102736874 26863196 MeRIP-seq:(Medium) rs751746726 Functional Loss SNV dbSNP153 33..33 33 - - - 71504 RMVar_ID_71504 Human_SNP_ID_85020897 m1A Human chr2 - 102736988 102736988 102736988 TGCTTACCGTATTGATGATGTGCCCAGTCCCCACCTTGCCTGAGACCAGAACTCCCAGCCAGCAC TGCTTACCGTATTGATGATGTGCCCAGTCCCCGCCTTGCCTGAGACCAGAACTCCCAGCCAGCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:102736945..102737018;chr2:102736940..102737044;chr2:102736944..102737046 26863196 MeRIP-seq:(Medium) rs1212651656 Functional Loss SNV dbSNP153 33..33 33 - - - 71505 RMVar_ID_71505 Human_SNP_ID_85570526 m1A Human chr2 + 104855348 104855321 104855348 GGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG GGGCGG___________________________AGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG GAGGCGGCGGCGGAGGAGGAGGCGGCGA G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:104855298..104855365 26863196 MeRIP-seq:(Medium) rs1323822424 Functional Loss DEL dbSNP153 7..33 33 - - - 71506 RMVar_ID_71506 Human_SNP_ID_85570536 m1A Human chr2 + 104855337 104855337 104855337 GGCGGCGGCGGGGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGG GGCGGCGGCGGGGGCGGAGGCGGCGGCGGAGGCGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGG A C AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr2:104855161..104855374;chr2:104855216..104855379 26863196 MeRIP-seq:(Medium) rs1246281511 Functional Loss SNV dbSNP153 33..33 33 - - - 71507 RMVar_ID_71507 Human_SNP_ID_85570537 m1A Human chr2 + 104855337 104855337 104855337 GGCGGCGGCGGGGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGG GGCGGCGGCGGGGGCGGAGGCGGCGGCGGAGGGGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGG A G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr2:104855161..104855374;chr2:104855216..104855379 26863196 MeRIP-seq:(Medium) rs1246281511 Functional Loss SNV dbSNP153 33..33 33 - - - 71508 RMVar_ID_71508 Human_SNP_ID_85570538 m1A Human chr2 + 104855348 104855339 104855348 GGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG GGGCGGAGGCGGCGGCGGAGGAGG_________AGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG GAGGCGGCGA G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:104855298..104855365 26863196 MeRIP-seq:(Medium) rs1256286214 Functional Loss DEL dbSNP153 25..33 33 - - - 71509 RMVar_ID_71509 Human_SNP_ID_85570546 m1A Human chr2 + 104855348 104855348 104855348 GGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGAAGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG GGGCGGAGGCGGCGGCGGAGGAGGAGGCGGCGGAGGCGGCGGGGCCGGCGGGGGCCCGGGGCGGG A G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:104855298..104855365 26863196 MeRIP-seq:(Medium) rs1447549644 Functional Loss SNV dbSNP153 33..33 33 - - - 71510 RMVar_ID_71510 Human_SNP_ID_85570742 m1A Human chr2 - 104855612 104855612 104855612 CCTGCGCCGCCCCCGCCGCCGCCGCCGCCGCCACCCCCGCCGCCGCCAGCCCCTGCCGCGTCCGA CCTGCGCCGCCCCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGCCGCCAGCCCCTGCCGCGTCCGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:104855508..104855634 26863196 MeRIP-seq:(Medium) rs547848317 Functional Loss SNV dbSNP153 33..33 33 - - - 71511 RMVar_ID_71511 Human_SNP_ID_85570743 m1A Human chr2 - 104855612 104855612 104855612 CCTGCGCCGCCCCCGCCGCCGCCGCCGCCGCCACCCCCGCCGCCGCCAGCCCCTGCCGCGTCCGA CCTGCGCCGCCCCCGCCGCCGCCGCCGCCGCCCCCCCCGCCGCCGCCAGCCCCTGCCGCGTCCGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:104855508..104855634 26863196 MeRIP-seq:(Medium) rs547848317 Functional Loss SNV dbSNP153 33..33 33 - - - 71512 RMVar_ID_71512 Human_SNP_ID_85570770 m1A Human chr2 + 104855642 104855642 104855642 GGTGGCGGCGGCGGCGGCGGCGGGGGCGGCGCAGGGGGCGGGGGCGGCGGCATGCAGCCGGGCAG GGTGGCGGCGGCGGCGGCGGCGGGGGCGGCGCGGGGGGCGGGGGCGGCGGCATGCAGCCGGGCAG A G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:104855585..104855709 26863196 MeRIP-seq:(Medium) rs923390131 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5198368,Human_RBP_ID_5296428 71513 RMVar_ID_71513 Human_SNP_ID_85571480 m1A Human chr2 + 104857205 104857205 104857205 TCCGCCGCCCTCCCCTCCACCCAGAGACAGGCATGCCCGCCCTTGGAGGAGAAAACGCGGGAGAA TCCGCCGCCCTCCCCTCCACCCAGAGACAGGCGTGCCCGCCCTTGGAGGAGAAAACGCGGGAGAA A G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:104856927..104857248 26863196 MeRIP-seq:(Medium) rs546349728 Functional Loss SNV dbSNP153 33..33 33 - - - 71514 RMVar_ID_71514 Human_SNP_ID_379918298 m1A Human chr8 + 120003078 120003078 120003078 GCGGCTACTTCAGCAGCAGCCCCACCCTCAGCAGCAGCCCCCCTGTGCTCTGCAACCCCAAGTCC GCGGCTACTTCAGCAGCAGCCCCACCCTCAGCGGCAGCCCCCCTGTGCTCTGCAACCCCAAGTCC A G DEPTOR Ensembl:ENSG00000155792 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:120002992..120003092 26863196 MeRIP-seq:(Medium) rs1178152606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1004035,Human_Splice_Rec_1004051,Human_Splice_Rec_1004061 Human_miRNA_ID_683251 RMVar_hsa_circ_55996,RMVar_hsa_circ_74339,RMVar_hsa_circ_254096,RMVar_hsa_circ_333888 71515 RMVar_ID_71515 Human_SNP_ID_380022896 m1A Human chr8 + 120445095 120445095 120445095 CTCACCTGGGGCGCCCTAGAGAAACTCGACATATTCCTCTACTAGCAGGACCGTACGTCCTTCTC CTCACCTGGGGCGCCCTAGAGAAACTCGACATGTTCCTCTACTAGCAGGACCGTACGTCCTTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:120445008..120445094 26863196 MeRIP-seq:(Medium) rs757784685 Functional Loss SNV dbSNP153 33..33 33 - - - 71516 RMVar_ID_71516 Human_SNP_ID_380023037 m1A Human chr8 - 120445490 120445490 120445490 CCGACGGGAATTTTCCTTCCCCCCAGATCACCAGCAGCAGGTACCGATCCATCTCCTCAGAGATC CCGACGGGAATTTTCCTTCCCCCCAGATCACCCGCAGCAGGTACCGATCCATCTCCTCAGAGATC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:120445439..120446443 26863196 MeRIP-seq:(Medium) rs1337473735 Functional Loss SNV dbSNP153 33..33 33 - - - 71517 RMVar_ID_71517 Human_SNP_ID_380652608 m1A Human chr8 - 123014660 123014660 123014660 GAGTTGCAGCTAACATGGGTTAGGTTTAAACCATGGGGGATGCAACCCCTTTGCGTTTCATATGT GAGTTGCAGCTAACATGGGTTAGGTTTAAACCGTGGGGGATGCAACCCCTTTGCGTTTCATATGT T C DERL1 Ensembl:ENSG00000136986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:123014609..123014710 32194978 MeRIP-seq:(Medium) rs1059588 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8728,GWAS_ID_8729,GWAS_ID_8730 71518 RMVar_ID_71518 Human_SNP_ID_380652850 m1A Human chr8 - 123015527 123015527 123015527 GAGGAGTATCAGGATTTGGTGTGCCCCCTGCTAGCATGAGGCGAGCTGCTGATCAGAATGGCGGA GAGGAGTATCAGGATTTGGTGTGCCCCCTGCTGGCATGAGGCGAGCTGCTGATCAGAATGGCGGA T C DERL1 Ensembl:ENSG00000136986 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:123015476..123015575 32194978 MeRIP-seq:(Medium) rs773906113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693881,Human_RBP_ID_957834,Human_RBP_ID_18124729,Human_RBP_ID_22115524,Human_RBP_ID_22775751,Human_RBP_ID_26189035 Human_Splice_Rec_1004996,Human_Splice_Rec_1005020,Human_Splice_Rec_1005026,Human_Splice_Rec_1005038,Human_Splice_Rec_1005050 RMVar_hsa_circ_254126 71519 RMVar_ID_71519 Human_SNP_ID_380682445 m1A Human chr8 + 123142406 123142406 123142406 AGGAAGTAGCCAAACTCCTTAGGGAAAACAGAAGGAAAGAAATAGAGATAATAAATGCAATGGTG AGGAAGTAGCCAAACTCCTTAGGGAAAACAGACGGAAAGAAATAGAGATAATAAATGCAATGGTG A C TBC1D31 Ensembl:ENSG00000156787 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123142357..123142492 26863196 MeRIP-seq:(Medium) rs141224192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1005097,Human_Splice_Rec_1005175,Human_Splice_Rec_1005227,Human_Splice_Rec_1005321 RMVar_hsa_circ_338515,RMVar_hsa_circ_297281,RMVar_hsa_circ_298414,RMVar_hsa_circ_254138,RMVar_hsa_circ_254136,RMVar_hsa_circ_254137,RMVar_hsa_circ_42520,RMVar_hsa_circ_254163,RMVar_hsa_circ_54817,RMVar_hsa_circ_341130,RMVar_hsa_circ_319544,RMVar_hsa_circ_320179,RMVar_hsa_circ_254164,RMVar_hsa_circ_254165,RMVar_hsa_circ_376931,RMVar_hsa_circ_66904,RMVar_hsa_circ_254166,RMVar_hsa_circ_64145,RMVar_hsa_circ_56825,RMVar_hsa_circ_64996,RMVar_hsa_circ_317901,RMVar_hsa_circ_254168,RMVar_hsa_circ_292899,RMVar_hsa_circ_254167,RMVar_hsa_circ_318559,RMVar_hsa_circ_254169 71520 RMVar_ID_71520 Human_SNP_ID_380682904 m1A Human chr8 + 123144672 123144672 123144672 GAAGTGGCTCATTCCACTGTGAAATGTGTATTACTATACTTTTTATGTAATCTTTTTTTCCATTT GAAGTGGCTCATTCCACTGTGAAATGTGTATTGCTATACTTTTTATGTAATCTTTTTTTCCATTT A G TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123144670..123144769 26863196 MeRIP-seq:(Medium) rs1463591815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338515,RMVar_hsa_circ_298414,RMVar_hsa_circ_254136,RMVar_hsa_circ_254137,RMVar_hsa_circ_42520,RMVar_hsa_circ_341130,RMVar_hsa_circ_320179,RMVar_hsa_circ_254164,RMVar_hsa_circ_254165,RMVar_hsa_circ_66904,RMVar_hsa_circ_254166,RMVar_hsa_circ_64145,RMVar_hsa_circ_56825,RMVar_hsa_circ_317901,RMVar_hsa_circ_254168,RMVar_hsa_circ_254167,RMVar_hsa_circ_318559 71521 RMVar_ID_71521 Human_SNP_ID_380685882 m1A Human chr8 - 123157245 123157245 123157245 GTCAGTCTCATAATCTGAAGGTCGTGAGTTCGATCCTCACACGGGGCACAATAATTTTGTTTGCT GTCAGTCTCATAATCTGAAGGTCGTGAGTTCGGTCCTCACACGGGGCACAATAATTTTGTTTGCT T C piR-33535,piR-33536,tRNA-Met-CAT-1-1,AB330778 RNACentral:URS00001402CA,RNACentral:URS000008DCBE,RNACentral:URS0000145C5E,RNACentral:URS00000DDDCA piRNA,piRNA,tRNA,misc_RNA exon,exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1269511367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693940,Human_RBP_ID_1145882,Human_RBP_ID_1223482,Human_RBP_ID_1247104,Human_RBP_ID_1400482,Human_RBP_ID_1700265,Human_RBP_ID_2052381,Human_RBP_ID_3134583,Human_RBP_ID_3872748,Human_RBP_ID_5223257,Human_RBP_ID_5270277,Human_RBP_ID_5430126,Human_RBP_ID_5453115,Human_RBP_ID_5480649,Human_RBP_ID_5514312,Human_RBP_ID_5536149,Human_RBP_ID_7808686,Human_RBP_ID_8273896,Human_RBP_ID_8679078,Human_RBP_ID_8916316,Human_RBP_ID_9312305,Human_RBP_ID_16339435,Human_RBP_ID_17714090,Human_RBP_ID_18112471,Human_RBP_ID_18211865,Human_RBP_ID_18452189,Human_RBP_ID_18541399,Human_RBP_ID_18891379,Human_RBP_ID_21581215,Human_RBP_ID_22836177,Human_RBP_ID_23088185,Human_RBP_ID_23112169,Human_RBP_ID_23140561,Human_RBP_ID_23199048,Human_RBP_ID_24244008,Human_RBP_ID_24440377,Human_RBP_ID_24518471,Human_RBP_ID_26189685,Human_RBP_ID_26751955,Human_RBP_ID_27128103,Human_RBP_ID_27362284,Human_RBP_ID_27773795 71522 RMVar_ID_71522 Human_SNP_ID_380707314 m1A Human chr8 - 123239146 123239146 123239146 TCACTCTGTAATAGGCTATTTTCATGATTTCAAGTGGTTTTATGAAGAAACAGAAAGCAGTGATG TCACTCTGTAATAGGCTATTTTCATGATTTCAGGTGGTTTTATGAAGAAACAGAAAGCAGTGATG T C C8orf76,ZHX1-C8orf76 Ensembl:ENSG00000189376,Ensembl:ENSG00000259305 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123239123..123239206 26863196 MeRIP-seq:(Medium) rs367713094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959319 Human_Splice_Rec_1005417,Human_Splice_Rec_1005427,Human_Splice_Rec_1005441,Human_Splice_Rec_1005447,Human_Splice_Rec_1005457,Human_Splice_Rec_1005467 71523 RMVar_ID_71523 Human_SNP_ID_380707887 m1A Human chr8 + 123241312 123241311 123241312 GCTCCGGCCTCTCCTCGAACACCGAGTCCTCGAACTCGCCGCCGAACAACCAGCACCCGGAATCC GCTCCGGCCTCTCCTCGAACACCGAGTCCTCG_ACTCGCCGCCGAACAACCAGCACCCGGAATCC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123241238..123241327 26863196 MeRIP-seq:(Medium) rs1457128084 Functional Loss DEL dbSNP153 33..33 33 - - - 71524 RMVar_ID_71524 Human_SNP_ID_380738726 m1A Human chr8 + 123369101 123369101 123369101 TTTACAGTAAGGACTTCTTGGTCCTGCGGAAGATAATCGGTATCTTGGTCTTGCAGGAGAAGCTG TTTACAGTAAGGACTTCTTGGTCCTGCGGAAGGTAATCGGTATCTTGGTCTTGCAGGAGAAGCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:123369051..123369100 32194978 MeRIP-seq:(Medium) rs1395638311 Functional Loss SNV dbSNP153 33..33 33 - - - 71525 RMVar_ID_71525 Human_SNP_ID_380739045 m1A Human chr8 - 123369952 123369952 123369952 TGGTGAAGATGAAGATGATGAAGATGATGATGATGATGACGATGATGATGATGATGATGATGATG TGGTGAAGATGAAGATGATGAAGATGATGATGGTGATGACGATGATGATGATGATGATGATGATG T C ATAD2 Ensembl:ENSG00000156802 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123369901..123370025 26863196 MeRIP-seq:(Medium) rs756903115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_217829,Human_RBP_ID_959329,Human_RBP_ID_1700114,Human_RBP_ID_3134931,Human_RBP_ID_4970031,Human_RBP_ID_7809335,Human_RBP_ID_8273903,Human_RBP_ID_9351660,Human_RBP_ID_9405750,Human_RBP_ID_18472505,Human_RBP_ID_18541411,Human_RBP_ID_19023001,Human_RBP_ID_21995565,Human_RBP_ID_23087907,Human_RBP_ID_23117127,Human_RBP_ID_24244220,Human_RBP_ID_24549417,Human_RBP_ID_26359348,Human_RBP_ID_27831552 Human_Splice_Rec_1005508,Human_Splice_Rec_1005560,Human_Splice_Rec_1005616,Human_Splice_Rec_1005670,Human_Splice_Rec_1005724 RMVar_hsa_circ_47794,RMVar_hsa_circ_266235,RMVar_hsa_circ_50757,RMVar_hsa_circ_338266,RMVar_hsa_circ_307644,RMVar_hsa_circ_254200,RMVar_hsa_circ_69779,RMVar_hsa_circ_30837,RMVar_hsa_circ_254202,RMVar_hsa_circ_254203,RMVar_hsa_circ_354799,RMVar_hsa_circ_284660,RMVar_hsa_circ_53699,RMVar_hsa_circ_254204,RMVar_hsa_circ_254205,RMVar_hsa_circ_68072,RMVar_hsa_circ_359350,RMVar_hsa_circ_82743,RMVar_hsa_circ_64183,RMVar_hsa_circ_72393,RMVar_hsa_circ_254208,RMVar_hsa_circ_254209,RMVar_hsa_circ_254211,RMVar_hsa_circ_354532,RMVar_hsa_circ_362895,RMVar_hsa_circ_265431,RMVar_hsa_circ_353920,RMVar_hsa_circ_268202,RMVar_hsa_circ_354950,RMVar_hsa_circ_267706,RMVar_hsa_circ_54047 71526 RMVar_ID_71526 Human_SNP_ID_380739061 m1A Human chr8 + 123369966 123369963 123369966 TCATCATCATCGTCATCATCATCATCATCTTCATCATCTTCATCTTCACCATCATCTTCATGTTC TCATCATCATCGTCATCATCATCATCATCT___TCATCTTCATCTTCACCATCATCTTCATGTTC TTCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:123369915..123369985 26863196 MeRIP-seq:(Medium) rs1554645798 Functional Loss DEL dbSNP153 31..33 33 - - - 71527 RMVar_ID_71527 Human_SNP_ID_380739067 m1A Human chr8 + 123369966 123369966 123369966 TCATCATCATCGTCATCATCATCATCATCTTCATCATCTTCATCTTCACCATCATCTTCATGTTC TCATCATCATCGTCATCATCATCATCATCTTCTTCATCTTCATCTTCACCATCATCTTCATGTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:123369915..123369985 26863196 MeRIP-seq:(Medium) rs995715139 Functional Loss SNV dbSNP153 33..33 33 - - - 71528 RMVar_ID_71528 Human_SNP_ID_380741923 m1A Human chr8 - 123380676 123380676 123380676 ACTTAGATGGCTTTCTTAATTTTTCTTAAAGGATGGGTCATCAGTTAAGGAAGTTGAAACCTACC ACTTAGATGGCTTTCTTAATTTTTCTTAAAGGGTGGGTCATCAGTTAAGGAAGTTGAAACCTACC T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:123380651..123380700 32194978 MeRIP-seq:(Medium) rs1461387837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3134976,Human_RBP_ID_21581758 Human_Splice_Rec_1005550,Human_Splice_Rec_1005606,Human_Splice_Rec_1005660,Human_Splice_Rec_1005714 RMVar_hsa_circ_266235,RMVar_hsa_circ_307644,RMVar_hsa_circ_254200,RMVar_hsa_circ_284660,RMVar_hsa_circ_254204,RMVar_hsa_circ_68072,RMVar_hsa_circ_359350,RMVar_hsa_circ_254209,RMVar_hsa_circ_254211,RMVar_hsa_circ_354532,RMVar_hsa_circ_353920,RMVar_hsa_circ_354950,RMVar_hsa_circ_366839,RMVar_hsa_circ_284378,RMVar_hsa_circ_322108,RMVar_hsa_circ_364206,RMVar_hsa_circ_254212 71529 RMVar_ID_71529 Human_SNP_ID_380745778 m1A Human chr8 - 123395115 123395115 123395115 ACCTGAGAGAAGGTTGGGAACTTGGGAATGAGAATGAGAGGCTCAGGGGAAATGTGTGGTGGAAG ACCTGAGAGAAGGTTGGGAACTTGGGAATGAGCATGAGAGGCTCAGGGGAAATGTGTGGTGGAAG T G ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:123395113..123395184 26863196 MeRIP-seq:(Medium) rs778469884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16342332 71530 RMVar_ID_71530 Human_SNP_ID_380746225 m1A Human chr8 - 123396382 123396382 123396382 GCGCCTGGAGCTGGATCTCTCTCCGGTCGCGCACGCCGAGGCCAGTAGGGAGAGAAGATGGTGGT GCGCCTGGAGCTGGATCTCTCTCCGGTCGCGCGCGCCGAGGCCAGTAGGGAGAGAAGATGGTGGT T C ATAD2 Ensembl:ENSG00000156802 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:123396137..123396425;chr8:123396276..123396425 26863196 MeRIP-seq:(Medium) rs368469577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254922,Human_RBP_ID_4970072,Human_RBP_ID_8923190,Human_RBP_ID_9312329,Human_RBP_ID_9405762,Human_RBP_ID_18426892,Human_RBP_ID_18452200,Human_RBP_ID_18891576,Human_RBP_ID_23087911,Human_RBP_ID_23120795,Human_RBP_ID_26358749,Human_RBP_ID_27832138 Human_miRNA_ID_2017783,Human_miRNA_ID_2155610,Human_miRNA_ID_2159172 RMVar_hsa_circ_100420,RMVar_hsa_circ_254213 71531 RMVar_ID_71531 Human_SNP_ID_380746226 m1A Human chr8 - 123396382 123396382 123396382 GCGCCTGGAGCTGGATCTCTCTCCGGTCGCGCACGCCGAGGCCAGTAGGGAGAGAAGATGGTGGT GCGCCTGGAGCTGGATCTCTCTCCGGTCGCGCCCGCCGAGGCCAGTAGGGAGAGAAGATGGTGGT T G ATAD2 Ensembl:ENSG00000156802 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:123396137..123396425;chr8:123396276..123396425 26863196 MeRIP-seq:(Medium) rs368469577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254922,Human_RBP_ID_4970072,Human_RBP_ID_8923190,Human_RBP_ID_9312329,Human_RBP_ID_9405762,Human_RBP_ID_18426892,Human_RBP_ID_18452200,Human_RBP_ID_18891576,Human_RBP_ID_23087911,Human_RBP_ID_23120795,Human_RBP_ID_26358749,Human_RBP_ID_27832138 Human_miRNA_ID_2017783,Human_miRNA_ID_2155610,Human_miRNA_ID_2159172 RMVar_hsa_circ_100420,RMVar_hsa_circ_254213 71532 RMVar_ID_71532 Human_SNP_ID_380746239 m1A Human chr8 + 123396395 123396394 123396395 CTCCCTACTGGCCTCGGCGTGCGCGACCGGAGAGAGATCCAGCTCCAGGCGCTCGCAGCTCTGGC CTCCCTACTGGCCTCGGCGTGCGCGACCGGAG_GAGATCCAGCTCCAGGCGCTCGCAGCTCTGGC GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123396294..123396398 26863196 MeRIP-seq:(Medium) rs773462294 Functional Loss DEL dbSNP153 33..33 33 - - - 71533 RMVar_ID_71533 Human_SNP_ID_380746241 m1A Human chr8 + 123396395 123396395 123396395 CTCCCTACTGGCCTCGGCGTGCGCGACCGGAGAGAGATCCAGCTCCAGGCGCTCGCAGCTCTGGC CTCCCTACTGGCCTCGGCGTGCGCGACCGGAGGGAGATCCAGCTCCAGGCGCTCGCAGCTCTGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123396294..123396398 26863196 MeRIP-seq:(Medium) rs751629439 Functional Loss SNV dbSNP153 33..33 33 - - - 71534 RMVar_ID_71534 Human_SNP_ID_380746258 m1A Human chr8 + 123396403 123396403 123396403 TGGCCTCGGCGTGCGCGACCGGAGAGAGATCCAGCTCCAGGCGCTCGCAGCTCTGGCTCTTCCGC TGGCCTCGGCGTGCGCGACCGGAGAGAGATCCGGCTCCAGGCGCTCGCAGCTCTGGCTCTTCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123396266..123396425 26863196 MeRIP-seq:(Medium) rs746487189 Functional Loss SNV dbSNP153 33..33 33 - - - 71535 RMVar_ID_71535 Human_SNP_ID_380751395 m1A Human chr8 - 123416639 123416639 123416639 CGGGACTAGCAGCACGAGTTCCCGGCGCGGGAAGCCCGGGACGAAGTAGGCGGAGCTCGGGGCAA CGGGACTAGCAGCACGAGTTCCCGGCGCGGGAGGCCCGGGACGAAGTAGGCGGAGCTCGGGGCAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123416588..123416746 26863196 MeRIP-seq:(Medium) rs547012971 Functional Loss SNV dbSNP153 33..33 33 - - - 71536 RMVar_ID_71536 Human_SNP_ID_380751489 m1A Human chr8 - 123416841 123416841 123416841 AGCAGCGGGGCCATTACCTTCCATGGCCGGCTAGCTGGGCCAGGGCCCGGGCCGGAGGAAGACCG AGCAGCGGGGCCATTACCTTCCATGGCCGGCTGGCTGGGCCAGGGCCCGGGCCGGAGGAAGACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:123416724..123416874 26863196 MeRIP-seq:(Medium) rs1484163466 Functional Loss SNV dbSNP153 33..33 33 - - - 71537 RMVar_ID_71537 Human_SNP_ID_380781734 m1A Human chr8 + 123541136 123541136 123541136 GGGGCCCGCGACGGGGGCGGCGGGGCGGCGGGAACGGCGCGGGGCACCCTGCGGGGTGGCGGGCG GGGGCCCGCGACGGGGGCGGCGGGGCGGCGGGGACGGCGCGGGGCACCCTGCGGGGTGGCGGGCG A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:123541045..123541175 26863410 MeRIP-seq:(Medium) rs1410432651 Functional Loss SNV dbSNP153 33..33 33 - - - 71538 RMVar_ID_71538 Human_SNP_ID_380846233 m1A Human chr8 + 123802248 123802248 123802248 GTTTAGATAAGAGATAAAGATAGCCCGGATCAAGGACATGGTAATAAGAATTGAAAGGAAAAATG GTTTAGATAAGAGATAAAGATAGCCCGGATCAGGGACATGGTAATAAGAATTGAAAGGAAAAATG A G FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123802208..123802682 26863196 MeRIP-seq:(Medium) rs1043737479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16343048 RMVar_hsa_circ_61077,RMVar_hsa_circ_91949,RMVar_hsa_circ_366497,RMVar_hsa_circ_8436,RMVar_hsa_circ_254226,RMVar_hsa_circ_108079,RMVar_hsa_circ_254225,RMVar_hsa_circ_108974,RMVar_hsa_circ_92921,RMVar_hsa_circ_254230,RMVar_hsa_circ_254231,RMVar_hsa_circ_363623 71539 RMVar_ID_71539 Human_SNP_ID_380848243 m1A Human chr8 - 123811238 123811231 123811238 CACACCGTGCTCCGGCCCTCTTCTTCAACCTTACCTCTTGCTTCTACCCCTCTTTCATGAAGTTT CACACCGTGCTCCGGCCCTCTTCTTCAACCTT_______GCTTCTACCCCTCTTTCATGAAGTTT CAAGAGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:123811187..123811290 26863196 MeRIP-seq:(Medium) rs1289572004 Functional Loss DEL dbSNP153 33..39 33 - - - 71540 RMVar_ID_71540 Human_SNP_ID_380848343 m1A Human chr8 + 123811694 123811694 123811694 GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCAATGATGGGCATACTGAGTATAGAGTGCATGGGG GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCAGTGATGGGCATACTGAGTATAGAGTGCATGGGG A G FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123811648..123811811 26863196 MeRIP-seq:(Medium) rs150629850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338708,Human_RBP_ID_16343243,Human_RBP_ID_22484254,Human_RBP_ID_24244439 RMVar_hsa_circ_91949,RMVar_hsa_circ_254225,RMVar_hsa_circ_108974,RMVar_hsa_circ_254231 71541 RMVar_ID_71541 Human_SNP_ID_380848344 m1A Human chr8 + 123811694 123811694 123811694 GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCAATGATGGGCATACTGAGTATAGAGTGCATGGGG GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCATTGATGGGCATACTGAGTATAGAGTGCATGGGG A T FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123811648..123811811 26863196 MeRIP-seq:(Medium) rs150629850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338708,Human_RBP_ID_16343243,Human_RBP_ID_22484254,Human_RBP_ID_24244439 RMVar_hsa_circ_91949,RMVar_hsa_circ_254225,RMVar_hsa_circ_108974,RMVar_hsa_circ_254231 71542 RMVar_ID_71542 Human_SNP_ID_380981111 m1A Human chr8 - 124371892 124371892 124371892 CCTGCACTCCACGGAGAGGAGCTGCCTGCTCAAAGAGCTGCACCGCTTCGAGTCTATTGCCATTG CCTGCACTCCACGGAGAGGAGCTGCCTGCTCAGAGAGCTGCACCGCTTCGAGTCTATTGCCATTG T C TMEM65 Ensembl:ENSG00000164983 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:124330782..124371944 26863196 MeRIP-seq:(Medium) rs540103095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8679414 Human_Splice_Rec_1006287 71543 RMVar_ID_71543 Human_SNP_ID_380981305 m1A Human chr8 - 124372326 124372326 124372326 CGGGCCTTTTGGAAAGGAAGTGGGGACGGAACAGGAGGCGAGAGCCGCGCGGGCCCGCGGAGTGC CGGGCCTTTTGGAAAGGAAGTGGGGACGGAACGGGAGGCGAGAGCCGCGCGGGCCCGCGGAGTGC T C TMEM65 Ensembl:ENSG00000164983 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:124372043..124372671 26863196 MeRIP-seq:(Medium) rs1420147148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255429,Human_RBP_ID_4996320,Human_RBP_ID_9338355 71544 RMVar_ID_71544 Human_SNP_ID_380981428 m1A Human chr8 - 124372651 124372651 124372651 GGTAGCGGCGGCGGCGGCGGCTGCGGCTCGGGAGCGCGGCTGCTTTGAGGGCTCGGGAACCTTAC GGTAGCGGCGGCGGCGGCGGCTGCGGCTCGGGGGCGCGGCTGCTTTGAGGGCTCGGGAACCTTAC T C TMEM65 Ensembl:ENSG00000164983 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:124372477..124372664 26863196 MeRIP-seq:(Medium) rs1046294377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4970226 71545 RMVar_ID_71545 Human_SNP_ID_381002002 m1A Human chr8 - 124450921 124450921 124450921 TTGCTAACAACCACATTCTCTCTCATCACCTCAGCGATACTCCATCTCCTCAGAGTCGGCTCACC TTGCTAACAACCACATTCTCTCTCATCACCTCGGCGATACTCCATCTCCTCAGAGTCGGCTCACC T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:124450870..124451038 26863196 MeRIP-seq:(Medium) rs768812661 Functional Loss SNV dbSNP153 33..33 33 - - - 71546 RMVar_ID_71546 Human_SNP_ID_381002003 m1A Human chr8 - 124450921 124450921 124450921 TTGCTAACAACCACATTCTCTCTCATCACCTCAGCGATACTCCATCTCCTCAGAGTCGGCTCACC TTGCTAACAACCACATTCTCTCTCATCACCTCCGCGATACTCCATCTCCTCAGAGTCGGCTCACC T G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:124450870..124451038 26863196 MeRIP-seq:(Medium) rs768812661 Functional Loss SNV dbSNP153 33..33 33 - - - 71547 RMVar_ID_71547 Human_SNP_ID_381007369 m1A Human chr8 - 124474402 124474402 124474402 GCTGCCTGGGAGAAGAAAAGCCAAAGGATGCCACCCTCTCGATTTATCCCACCCTCGGGAGTCTG GCTGCCTGGGAGAAGAAAAGCCAAAGGATGCCGCCCTCTCGATTTATCCCACCCTCGGGAGTCTG T C RNF139-AS1 Ensembl:ENSG00000245149 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:124474351..124474532 26863196 MeRIP-seq:(Medium) rs1261149977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105625,Human_RBP_ID_5658396,Human_RBP_ID_22115536,Human_RBP_ID_26360145,Human_RBP_ID_27832141 71548 RMVar_ID_71548 Human_SNP_ID_381007611 m1A Human chr8 + 124475002 124475002 124475002 GGGCTGGCCGTGAGAGAGACAGGAGAGGAAGGAGGGCAGGGGCGGAGTTGCCCGCCTTAGCCCCC GGGCTGGCCGTGAGAGAGACAGGAGAGGAAGGTGGGCAGGGGCGGAGTTGCCCGCCTTAGCCCCC A T RNF139 Ensembl:ENSG00000170881 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:124474901..124475088 26863410 MeRIP-seq:(Medium) rs1336504301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996324,Human_RBP_ID_8238743,Human_RBP_ID_9338710 71549 RMVar_ID_71549 Human_SNP_ID_381023910 m1A Human chr8 - 124539215 124539215 124539215 TATAAAGCCGCAACACCTTTTGCTGATGGGTCAGGTAGGGTCCCGACGCCAAGAACGCCATTACG TATAAAGCCGCAACACCTTTTGCTGATGGGTCCGGTAGGGTCCCGACGCCAAGAACGCCATTACG T G TATDN1 Ensembl:ENSG00000147687 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr8:124539126..124539337;chr8:124539126..124539300;chr8:124539126..124539252 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1458680483 Functional Loss SNV dbSNP153 33..33 33 - - - 71550 RMVar_ID_71550 Human_SNP_ID_381023936 m1A Human chr8 + 124539269 124539269 124539269 GCGGCTTTATAAGCGGGCGCTACGCCACCTCGAGTCGTGGTGCGTCCAGAGGTAAGGGATGGGGA GCGGCTTTATAAGCGGGCGCTACGCCACCTCGGGTCGTGGTGCGTCCAGAGGTAAGGGATGGGGA A G TATDN1 Ensembl:ENSG00000147687 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs200160068 Functional Loss SNV dbSNP153 33..33 33 - - - 71551 RMVar_ID_71551 Human_SNP_ID_381026468 m1A Human chr8 - 124549715 124549713 124549716 AGGAAGGAATCATTACCAAAGGAATCTAATTGACTATAAAAATCTGTCTGCTGCAGTGAAGGGTC AGGAAGGAATCATTACCAAAGGAATCTAATT___TATAAAAATCTGTCTGCTGCAGTGAAGGGTC AGTC A RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:124549712..124549900 26863196 MeRIP-seq:(Medium) rs1292803642 Functional Loss DEL dbSNP153 32..34 33 - - - 71552 RMVar_ID_71552 Human_SNP_ID_381026470 m1A Human chr8 - 124549715 124549715 124549715 AGGAAGGAATCATTACCAAAGGAATCTAATTGACTATAAAAATCTGTCTGCTGCAGTGAAGGGTC AGGAAGGAATCATTACCAAAGGAATCTAATTGGCTATAAAAATCTGTCTGCTGCAGTGAAGGGTC T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:124549712..124549900 26863196 MeRIP-seq:(Medium) rs973485223 Functional Loss SNV dbSNP153 33..33 33 - - - 71553 RMVar_ID_71553 Human_SNP_ID_381069617 m1A Human chr8 - 124728003 124728003 124728003 TTCTGGGGTGAGCGAGCCCCGGCCCCGCGCGCAGTCCAGCGGCCCCGCGTGTGTGCCCTCGCCCT TTCTGGGGTGAGCGAGCCCCGGCCCCGCGCGCCGTCCAGCGGCCCCGCGTGTGTGCCCTCGCCCT T G MTSS1 Ensembl:ENSG00000170873 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:124727958..124728071 26863196 MeRIP-seq:(Medium) rs773742116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996333 71554 RMVar_ID_71554 Human_SNP_ID_381133383 m1A Human chr8 + 124998649 124998649 124998649 GTCGGGAGCCGCCGCCGCCATCTGAGGGAGGTACCCTGGAAACCACCTTTTATCGGTGGGGAAGT GTCGGGAGCCGCCGCCGCCATCTGAGGGAGGTCCCCTGGAAACCACCTTTTATCGGTGGGGAAGT A C SQLE Ensembl:ENSG00000104549 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:124998557..124998651 26863410 MeRIP-seq:(Medium) rs1165191672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845317,Human_RBP_ID_4970458,Human_RBP_ID_5329197,Human_RBP_ID_5534313,Human_RBP_ID_8944472,Human_RBP_ID_22465647,Human_RBP_ID_27535762 RMVar_hsa_circ_95102,RMVar_hsa_circ_254266 71555 RMVar_ID_71555 Human_SNP_ID_381133384 m1A Human chr8 + 124998649 124998649 124998649 GTCGGGAGCCGCCGCCGCCATCTGAGGGAGGTACCCTGGAAACCACCTTTTATCGGTGGGGAAGT GTCGGGAGCCGCCGCCGCCATCTGAGGGAGGTGCCCTGGAAACCACCTTTTATCGGTGGGGAAGT A G SQLE Ensembl:ENSG00000104549 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:124998557..124998651 26863410 MeRIP-seq:(Medium) rs1165191672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845317,Human_RBP_ID_4970458,Human_RBP_ID_5329197,Human_RBP_ID_5534313,Human_RBP_ID_8944472,Human_RBP_ID_22465647,Human_RBP_ID_27535762 RMVar_hsa_circ_95102,RMVar_hsa_circ_254266 71556 RMVar_ID_71556 Human_SNP_ID_381133538 m1A Human chr8 + 124999073 124999073 124999073 CAGTATCAGAAGAGTATCCATCACCCGCAGCAACCGCTCAGGGAACACCATCAAAAAAGAAAAAA CAGTATCAGAAGAGTATCCATCACCCGCAGCAGCCGCTCAGGGAACACCATCAAAAAAGAAAAAA A G SQLE Ensembl:ENSG00000104549 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:124999026..124999700 32194978 MeRIP-seq:(Medium) rs7012867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960554,Human_RBP_ID_4995187,Human_RBP_ID_8944477,Human_RBP_ID_27120685 Human_miRNA_ID_1972915,Human_miRNA_ID_1975090,Human_miRNA_ID_2612900,Human_miRNA_ID_2958984,Human_miRNA_ID_3001210 RMVar_hsa_circ_95102,RMVar_hsa_circ_254266 71557 RMVar_ID_71557 Human_SNP_ID_381134702 m1A Human chr8 + 125003183 125003183 125003183 AGTTTACCTTTTTTTTTTTAAACAGCGCAGAAAAGGAACCAATATTTCAGAAACAAGCTTAATAG AGTTTACCTTTTTTTTTTTAAACAGCGCAGAAGAGGAACCAATATTTCAGAAACAAGCTTAATAG A G SQLE Ensembl:ENSG00000104549 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:125003176..125005535 32194978 MeRIP-seq:(Medium) rs766514291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17319605,Human_RBP_ID_17434054,Human_RBP_ID_22115740,Human_RBP_ID_22775915,Human_RBP_ID_27362492 Human_Splice_Rec_1007408,Human_Splice_Rec_1007428,Human_Splice_Rec_1007450 RMVar_hsa_circ_95102,RMVar_hsa_circ_254267,RMVar_hsa_circ_286336,RMVar_hsa_circ_359111,RMVar_hsa_circ_254266,RMVar_hsa_circ_319223,RMVar_hsa_circ_254268 71558 RMVar_ID_71558 Human_SNP_ID_381139118 m1A Human chr8 + 125021848 125021848 125021848 TTTTTGCTTTAAGTCAGAACCTTGGATTACAAAACCTCGAGCCCTTCTCAGTAGTGGTGCTGTAT TTTTTGCTTTAAGTCAGAACCTTGGATTACAAGACCTCGAGCCCTTCTCAGTAGTGGTGCTGTAT A G SQLE Ensembl:ENSG00000104549 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:125020923..125021937 32194978 MeRIP-seq:(Medium) rs990810017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123806,Human_RBP_ID_9264186,Human_RBP_ID_16346023,Human_RBP_ID_17319618,Human_RBP_ID_17544523,Human_RBP_ID_21906128,Human_RBP_ID_22775930,Human_RBP_ID_24245017 Human_Splice_Rec_1007426,Human_Splice_Rec_1007446 RMVar_hsa_circ_90476,RMVar_hsa_circ_76296,RMVar_hsa_circ_254271,RMVar_hsa_circ_97756,RMVar_hsa_circ_102995,RMVar_hsa_circ_254276,RMVar_hsa_circ_254277,RMVar_hsa_circ_254278 71559 RMVar_ID_71559 Human_SNP_ID_381150319 m1A Human chr8 + 125066773 125066771 125066773 GCCAACTGGTCTTTCAGGTCTTTGAATTGTTTATGTTCCTCCTCACCAAAGACGACTTGATATTC GCCAACTGGTCTTTCAGGTCTTTGAATTGTT__TGTTCCTCCTCACCAAAGACGACTTGATATTC TTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125066722..125066863 26863196 MeRIP-seq:(Medium) rs1377425373 Functional Loss DEL dbSNP153 32..33 33 - - - 71560 RMVar_ID_71560 Human_SNP_ID_381156682 m1A Human chr8 - 125091712 125091712 125091712 TGACCCGCTCCAGGTCCGGGACTGCGGATAGAAGAGGACCGCCGCCTTGAGGGAGGGGTGGAAAC TGACCCGCTCCAGGTCCGGGACTGCGGATAGAGGAGGACCGCCGCCTTGAGGGAGGGGTGGAAAC T C WASHC5 Ensembl:ENSG00000164961 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:125091627..125091735;chr8:125091637..125091740 26863196 MeRIP-seq:(Medium) rs1190205243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4970584,Human_RBP_ID_8923198 Human_Splice_Rec_1007469,Human_Splice_Rec_1007523,Human_Splice_Rec_1007577,Human_Splice_Rec_1007587,Human_Splice_Rec_1007593 71561 RMVar_ID_71561 Human_SNP_ID_381156791 m1A Human chr8 + 125091936 125091936 125091936 GGTCTAGGCAGGGGAAATTGGGGTGCCACCAGACGGAGACAGCTTGGACTACCAGGTAGGGAAGA GGTCTAGGCAGGGGAAATTGGGGTGCCACCAGTCGGAGACAGCTTGGACTACCAGGTAGGGAAGA A T NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:125091886..125092021 26863196 MeRIP-seq:(Medium) rs897376816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5405946,Human_RBP_ID_7810983,Human_RBP_ID_18426748 Human_Splice_Rec_1007619,Human_Splice_Rec_1007627,Human_Splice_Rec_1007639,Human_Splice_Rec_1007653,Human_Splice_Rec_1007659,Human_Splice_Rec_1007665,Human_Splice_Rec_1007677 RMVar_hsa_circ_85279,RMVar_hsa_circ_254296 71562 RMVar_ID_71562 Human_SNP_ID_381158632 m1A Human chr8 + 125099910 125099910 125099910 GATGGGAGAAGTAATGGTGTATTTGTTTGCTGAAGGGAATGATTCAGTAGAGAGGGAAAATTTAA GATGGGAGAAGTAATGGTGTATTTGTTTGCTGGAGGGAATGATTCAGTAGAGAGGGAAAATTTAA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:125099905..125100066 26863196 MeRIP-seq:(Medium) rs992955705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24245101 RMVar_hsa_circ_9305,RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254297 71563 RMVar_ID_71563 Human_SNP_ID_381158651 m1A Human chr8 + 125100014 125100014 125100014 TAGAGTAGGGAGGGAGGGATAGGATCTAGTGGATAATTGGAGTGGAGGTGGCCTTATCTAGGAGC TAGAGTAGGGAGGGAGGGATAGGATCTAGTGGCTAATTGGAGTGGAGGTGGCCTTATCTAGGAGC A C NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125100010..125100093 26863196 MeRIP-seq:(Medium) rs1039703989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9305,RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254297 71564 RMVar_ID_71564 Human_SNP_ID_381158652 m1A Human chr8 + 125100014 125100014 125100014 TAGAGTAGGGAGGGAGGGATAGGATCTAGTGGATAATTGGAGTGGAGGTGGCCTTATCTAGGAGC TAGAGTAGGGAGGGAGGGATAGGATCTAGTGGGTAATTGGAGTGGAGGTGGCCTTATCTAGGAGC A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125100010..125100093 26863196 MeRIP-seq:(Medium) rs1039703989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9305,RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254297 71565 RMVar_ID_71565 Human_SNP_ID_381184306 m1A Human chr8 + 125212443 125212443 125212443 TAGAGCTGAGGCAGTGAGAGCCCGGTATGTGCAGGAGGCTTTGTTCATGGCCAGACTATTGTGGG TAGAGCTGAGGCAGTGAGAGCCCGGTATGTGCGGGAGGCTTTGTTCATGGCCAGACTATTGTGGG A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:125212439..125212509 26863196 MeRIP-seq:(Medium) rs1030425909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71566 RMVar_ID_71566 Human_SNP_ID_381205159 m1A Human chr8 - 125300732 125300732 125300732 CTACATCAGGCCACCTTCCTTTCTACTCTCAAAGCACCTTGTACCTCCTCCACCATAATACACTT CTACATCAGGCCACCTTCCTTTCTACTCTCAAGGCACCTTGTACCTCCTCCACCATAATACACTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125300681..125300882 26863196 MeRIP-seq:(Medium) rs1341193277 Functional Loss SNV dbSNP153 33..33 33 - - - 71567 RMVar_ID_71567 Human_SNP_ID_381205558 m1A Human chr8 + 125302399 125302399 125302399 GAGTTGGCCTGGCACACATTCCAGGAGTGACAAGGAGGTTCCCATGGAATGAGTGAGGGAAAGGA GAGTTGGCCTGGCACACATTCCAGGAGTGACAGGGAGGTTCCCATGGAATGAGTGAGGGAAAGGA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125302387..125302475 26863196 MeRIP-seq:(Medium) rs566203226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71568 RMVar_ID_71568 Human_SNP_ID_381205991 m1A Human chr8 - 125304413 125304413 125304413 TACACTTTAGCACATACATCACGGGGCACTGAAGTCATCTCTCCTGAAACCTACATGGATCACGT TACACTTTAGCACATACATCACGGGGCACTGATGTCATCTCTCCTGAAACCTACATGGATCACGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125304407..125304533 26863196 MeRIP-seq:(Medium) rs1378952109 Functional Loss SNV dbSNP153 33..33 33 - - - 71569 RMVar_ID_71569 Human_SNP_ID_381206095 m1A Human chr8 + 125304884 125304883 125304884 CATTTCAGCCTGGGCAACAGAGCCAGACTCTGAAAAAAAAAAAAGAGAGAGAAAGAAAGGAAAGA CATTTCAGCCTGGGCAACAGAGCCAGACTCTG_AAAAAAAAAAAGAGAGAGAAAGAAAGGAAAGA GA G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:125304880..125305049 26863196 MeRIP-seq:(Medium) rs373087319 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71570 RMVar_ID_71570 Human_SNP_ID_381206107 m1A Human chr8 + 125304913 125304896 125304913 CTGAAAAAAAAAAAAGAGAGAGAAAGAAAGGAAAGAGAGAAAGAAAGAAGGAAAGAAAGGAAGGA CTGAAAAAAAAAAAAG_________________AGAGAGAAAGAAAGAAGGAAAGAAAGGAAGGA GAGAGAGAAAGAAAGGAA G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:125304910..125305051 26863196 MeRIP-seq:(Medium) rs1274600671 Functional Loss DEL dbSNP153 17..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71571 RMVar_ID_71571 Human_SNP_ID_381206111 m1A Human chr8 + 125304913 125304913 125304913 CTGAAAAAAAAAAAAGAGAGAGAAAGAAAGGAAAGAGAGAAAGAAAGAAGGAAAGAAAGGAAGGA CTGAAAAAAAAAAAAGAGAGAGAAAGAAAGGAGAGAGAGAAAGAAAGAAGGAAAGAAAGGAAGGA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:125304910..125305051 26863196 MeRIP-seq:(Medium) rs1242167367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71572 RMVar_ID_71572 Human_SNP_ID_381207903 m1A Human chr8 + 125313146 125313124 125313146 AGGGAAAGAAGGAAGGAAGGAAGGAGAAAGAAAGAAGGAAGGAAGGAAAAAAAGGAAGGAAAGAA AGGGAAAGAAG______________________GAAGGAAGGAAGGAAAAAAAGGAAGGAAAGAA GGAAGGAAGGAAGGAGAAAGAAA G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125313142..125313323 26863196 MeRIP-seq:(Medium) rs967065565 Functional Loss DEL dbSNP153 12..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71573 RMVar_ID_71573 Human_SNP_ID_381207909 m1A Human chr8 + 125313146 125313146 125313146 AGGGAAAGAAGGAAGGAAGGAAGGAGAAAGAAAGAAGGAAGGAAGGAAAAAAAGGAAGGAAAGAA AGGGAAAGAAGGAAGGAAGGAAGGAGAAAGAAGGAAGGAAGGAAGGAAAAAAAGGAAGGAAAGAA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:125313142..125313323 26863196 MeRIP-seq:(Medium) rs542957141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 71574 RMVar_ID_71574 Human_SNP_ID_381220993 m1A Human chr8 - 125367074 125367074 125367074 GTTTTATTTAACATTATAGAACACTTAAAAATAAACAATATGATTGCATTTCTGTTGTGTAACTT GTTTTATTTAACATTATAGAACACTTAAAAATGAACAATATGATTGCATTTCTGTTGTGTAACTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:125367026..125367125 32194978 MeRIP-seq:(Medium) rs1435991990 Functional Loss SNV dbSNP153 33..33 33 - - - 71575 RMVar_ID_71575 Human_SNP_ID_381237253 m1A Human chr8 - 125430692 125430692 125430692 CACGCGGGGACCACGCTGGCTGTGCGTCCGGGAGGCGGAGGCCGGCTCGAGTCCCCGGACCCCCG CACGCGGGGACCACGCTGGCTGTGCGTCCGGGGGGCGGAGGCCGGCTCGAGTCCCCGGACCCCCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:125430641..125430741 32194978 MeRIP-seq:(Medium) rs2280826 Functional Loss SNV dbSNP153 33..33 33 - - - 71576 RMVar_ID_71576 Human_SNP_ID_381515282 m1A Human chr8 + 126556160 126556160 126556160 AAGAATGGCCGATTATAAACCCAGATCTACCAAGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT AAGAATGGCCGATTATAAACCCAGATCTACCACGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT A C PCAT1 RNACentral:URS00009B75C9 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:126556109..126556259 32194978 MeRIP-seq:(Medium) rs967436456 Functional Loss SNV dbSNP153 33..33 33 - - - 71577 RMVar_ID_71577 Human_SNP_ID_381515283 m1A Human chr8 + 126556160 126556160 126556160 AAGAATGGCCGATTATAAACCCAGATCTACCAAGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT AAGAATGGCCGATTATAAACCCAGATCTACCATGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT A T PCAT1 RNACentral:URS00009B75C9 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:126556109..126556259 32194978 MeRIP-seq:(Medium) rs967436456 Functional Loss SNV dbSNP153 33..33 33 - - - 71578 RMVar_ID_71578 Human_SNP_ID_381515438 m1A Human chr8 - 126556551 126556551 126556551 CGCCACGCACCTGCACCCGGCGGAGCCGGAGGAGGGCGACAGCAACGTGGCGCGGACTACGCCGC CGCCACGCACCTGCACCCGGCGGAGCCGGAGGGGGGCGACAGCAACGTGGCGCGGACTACGCCGC T C LRATD2 Ensembl:ENSG00000168672 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:126556506..126556606 26863410 MeRIP-seq:(Medium) rs770726841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128082,RMVar_hsa_circ_254312 71579 RMVar_ID_71579 Human_SNP_ID_381515439 m1A Human chr8 - 126556551 126556551 126556551 CGCCACGCACCTGCACCCGGCGGAGCCGGAGGAGGGCGACAGCAACGTGGCGCGGACTACGCCGC CGCCACGCACCTGCACCCGGCGGAGCCGGAGGCGGGCGACAGCAACGTGGCGCGGACTACGCCGC T G LRATD2 Ensembl:ENSG00000168672 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:126556506..126556606 26863410 MeRIP-seq:(Medium) rs770726841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128082,RMVar_hsa_circ_254312 71580 RMVar_ID_71580 Human_SNP_ID_381516108 m1A Human chr8 - 126558254 126558254 126558254 CAGCCCCAGCTGGCGGGAGGAAGCGCGGTGTGAACAGGGATTGCCCCCCGCCTTCAAGTATCGGG CAGCCCCAGCTGGCGGGAGGAAGCGCGGTGTGGACAGGGATTGCCCCCCGCCTTCAAGTATCGGG T C LRATD2 Ensembl:ENSG00000168672 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:126558204..126558376 26863196 MeRIP-seq:(Medium) rs1028796617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996357 71581 RMVar_ID_71581 Human_SNP_ID_381516171 m1A Human chr8 - 126558404 126558404 126558404 GCCCGGAGCCGGATCTACAATCCCGTCCCTCCAGCTCCGGTGCTTGTTGCTCGCCCGGCCCAAGC GCCCGGAGCCGGATCTACAATCCCGTCCCTCCGGCTCCGGTGCTTGTTGCTCGCCCGGCCCAAGC T C LRATD2 Ensembl:ENSG00000168672 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:126558273..126558405 26863196 MeRIP-seq:(Medium) rs1317735133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5453156,Human_RBP_ID_5480685,Human_RBP_ID_5514374 71582 RMVar_ID_71582 Human_SNP_ID_381517921 m1A Human chr8 - 126565266 126565266 126565266 TCCCTTCGCCCCAGGCCAGATAGGAATGACCAACTGCATTTGTTGAGCCCTGTGTCCTAAATGCT TCCCTTCGCCCCAGGCCAGATAGGAATGACCAGCTGCATTTGTTGAGCCCTGTGTCCTAAATGCT T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:126565247..126565331 26863410 MeRIP-seq:(Medium) rs930506827 Functional Loss SNV dbSNP153 33..33 33 - - - 71583 RMVar_ID_71583 Human_SNP_ID_381663311 m1A Human chr8 - 127135725 127135725 127135725 TGTGCCAGTTAGTGGGTCACTAGAGACCCTGGAAGAACAGTTTCTCTGAAGGGATGAGGCCCATA TGTGCCAGTTAGTGGGTCACTAGAGACCCTGGGAGAACAGTTTCTCTGAAGGGATGAGGCCCATA T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:127135714..127135896 26863196 MeRIP-seq:(Medium) rs1487520921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8679802 71584 RMVar_ID_71584 Human_SNP_ID_381682906 m1A Human chr8 + 127211905 127211905 127211905 CCCATGGCCCCAGACAGAGGGCAGAGAATGAAACCTATTATCTTTCTGAACGTTCCTTCCCTCTT CCCATGGCCCCAGACAGAGGGCAGAGAATGAAGCCTATTATCTTTCTGAACGTTCCTTCCCTCTT A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:127211903..127211997 26863196 MeRIP-seq:(Medium) rs1210339078 Functional Loss SNV dbSNP153 33..33 33 - - - 71585 RMVar_ID_71585 Human_SNP_ID_381683113 m1A Human chr8 + 127212700 127212700 127212700 GGCACACAAACCTTCACAACCTGCCCTGCCCAAAGTTACACTGCTTCCTTCCTCCACACCCCACA GGCACACAAACCTTCACAACCTGCCCTGCCCAGAGTTACACTGCTTCCTTCCTCCACACCCCACA A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:127212651..127212813;chr8:127212653..127212803 26863196 MeRIP-seq:(Medium) rs1022085417 Functional Loss SNV dbSNP153 33..33 33 - - - 71586 RMVar_ID_71586 Human_SNP_ID_381684547 m1A Human chr8 + 127218581 127218581 127218581 CTCCATGTTTTAGCTTAGATATTGTTTCCTCCAGGCGGCCCTCCTTGACCTTCCAATTCTGGTTA CTCCATGTTTTAGCTTAGATATTGTTTCCTCCTGGCGGCCCTCCTTGACCTTCCAATTCTGGTTA A T PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127218531..127218617 26863196 MeRIP-seq:(Medium) rs1193345833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3138617 71587 RMVar_ID_71587 Human_SNP_ID_381684863 m1A Human chr8 + 127219530 127219530 127219530 GAACACCAGTGACTATGGCCTGAAGTTGCCCTAAGACAGTTTAAACATCCTGTTGATTGTTTTGT GAACACCAGTGACTATGGCCTGAAGTTGCCCTGAGACAGTTTAAACATCCTGTTGATTGTTTTGT A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127219492..127219568 26863196 MeRIP-seq:(Medium) rs1271515537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3138679 71588 RMVar_ID_71588 Human_SNP_ID_381685054 m1A Human chr8 - 127220254 127220254 127220254 GCAGGAACTTCCTGTTTCAATAACATTTCTCAATACTCTACCTGATTGCTTAGAATCCATGAGAC GCAGGAACTTCCTGTTTCAATAACATTTCTCAGTACTCTACCTGATTGCTTAGAATCCATGAGAC T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:127220203..127220334 26863196 MeRIP-seq:(Medium) rs1393495786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3138629,Human_RBP_ID_5631005,Human_RBP_ID_8680284,Human_RBP_ID_16352345,Human_RBP_ID_17200790,Human_RBP_ID_21564131,Human_RBP_ID_24440608,Human_RBP_ID_24519175,Human_RBP_ID_26152053,Human_RBP_ID_27540349 RMVar_hsa_circ_337858 71589 RMVar_ID_71589 Human_SNP_ID_381685542 m1A Human chr8 + 127221876 127221876 127221876 AAACCGGGAGGTGGAGGTTGCAGTGAGCCGGGATCACACCACTGCACTCCAGCCTGGGTGACAGA AAACCGGGAGGTGGAGGTTGCAGTGAGCCGGGCTCACACCACTGCACTCCAGCCTGGGTGACAGA A C PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:127221826..127221875 26863196 MeRIP-seq:(Medium) rs1176449133 Functional Loss SNV dbSNP153 33..33 33 - - - 71590 RMVar_ID_71590 Human_SNP_ID_381686249 m1A Human chr8 + 127224102 127224102 127224102 CCATCCAGCCTCATTTCTACTCTCCCTCCTTCATCTTTTTCCTTACTGATGTTACCACAAAATTC CCATCCAGCCTCATTTCTACTCTCCCTCCTTCGTCTTTTTCCTTACTGATGTTACCACAAAATTC A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:127224051..127224125 26863196 MeRIP-seq:(Medium) rs1269705579 Functional Loss SNV dbSNP153 33..33 33 - - - 71591 RMVar_ID_71591 Human_SNP_ID_381686760 m1A Human chr8 + 127226342 127226342 127226342 AGTTTGGGCTGTCTGAGAAACCAAAAGGAGAAAAGGAGAGAAGTGTCAGTAGAGTTCAGTGAGTG AGTTTGGGCTGTCTGAGAAACCAAAAGGAGAAGAGGAGAGAAGTGTCAGTAGAGTTCAGTGAGTG A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:127226326..127226350 26863196 MeRIP-seq:(Medium) rs1453105167 Functional Loss SNV dbSNP153 33..33 33 - - - 71592 RMVar_ID_71592 Human_SNP_ID_381686786 m1A Human chr8 + 127226450 127226450 127226450 GGCAGGTGCAGAAAGATCAAAATTGAGGTTTCAGTATTATGTGGGGAGGTAACCTAATTTGGTTT GGCAGGTGCAGAAAGATCAAAATTGAGGTTTCGGTATTATGTGGGGAGGTAACCTAATTTGGTTT A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:127226426..127226450 26863196 MeRIP-seq:(Medium) rs942665829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3139028 71593 RMVar_ID_71593 Human_SNP_ID_381691788 m1A Human chr8 - 127246138 127246138 127246138 TTCAAAATCTGTCTAGGGTCCATCCACCACTCACCACCTGGAATGCCACCCTGGTCCATGTTACC TTCAAAATCTGTCTAGGGTCCATCCACCACTCGCCACCTGGAATGCCACCCTGGTCCATGTTACC T C CASC19 RNACentral:URS00009B92B3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:127246088..127246225 26863196 MeRIP-seq:(Medium) rs184480597 Functional Loss SNV dbSNP153 33..33 33 - - - 71594 RMVar_ID_71594 Human_SNP_ID_381692184 m1A Human chr8 + 127247776 127247776 127247776 GATTTATAAAGAAGTGGCACAGGTTATAAGGGATTTTGCTGATGACTGATCTGGAATTGTACAAG GATTTATAAAGAAGTGGCACAGGTTATAAGGGGTTTTGCTGATGACTGATCTGGAATTGTACAAG A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:127247729..127247876 26863196 MeRIP-seq:(Medium) rs903457971 Functional Loss SNV dbSNP153 33..33 33 - - - 71595 RMVar_ID_71595 Human_SNP_ID_381694609 m1A Human chr8 + 127257101 127257101 127257101 CAATTATCAAAATCCTTTGGAGAATTTAGGGAAATTGAAGGAATGGGGCTTCTCGTGGCATGTGA CAATTATCAAAATCCTTTGGAGAATTTAGGGACATTGAAGGAATGGGGCTTCTCGTGGCATGTGA A C PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:127257076..127257100 26863196 MeRIP-seq:(Medium) rs1204598037 Functional Loss SNV dbSNP153 33..33 33 - - - 71596 RMVar_ID_71596 Human_SNP_ID_381694610 m1A Human chr8 + 127257101 127257101 127257101 CAATTATCAAAATCCTTTGGAGAATTTAGGGAAATTGAAGGAATGGGGCTTCTCGTGGCATGTGA CAATTATCAAAATCCTTTGGAGAATTTAGGGAGATTGAAGGAATGGGGCTTCTCGTGGCATGTGA A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:127257076..127257100 26863196 MeRIP-seq:(Medium) rs1204598037 Functional Loss SNV dbSNP153 33..33 33 - - - 71597 RMVar_ID_71597 Human_SNP_ID_381694759 m1A Human chr8 - 127257656 127257656 127257656 CCCGCTTCTCACTCCACAGGACCCCCATCCTCAAGCCCACTTCACACTCCCCAGTCATTTTCAAT CCCGCTTCTCACTCCACAGGACCCCCATCCTCCAGCCCACTTCACACTCCCCAGTCATTTTCAAT T G CASC19 RNACentral:URS00009B92B3 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:127257137..127258600 26863196 MeRIP-seq:(Medium) rs545069749 Functional Loss SNV dbSNP153 33..33 33 - - - 71598 RMVar_ID_71598 Human_SNP_ID_381815232 m1A Human chr8 + 127736616 127736616 127736616 TGCTTAGACGCTGGATTTTTTTCGGGTAGTGGAAAACCAGGTAAGCACCGAAGTCCACTTGCCTT TGCTTAGACGCTGGATTTTTTTCGGGTAGTGGGAAACCAGGTAAGCACCGAAGTCCACTTGCCTT A G MYC Ensembl:ENSG00000136997 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:127736301..127738337 32194978 MeRIP-seq:(Medium) rs759986640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3140042,Human_RBP_ID_4996365,Human_RBP_ID_18196549,Human_RBP_ID_19141738 Human_Splice_Rec_1008883,Human_Splice_Rec_1008889,Human_Splice_Rec_1008895,Human_Splice_Rec_1008899,Human_Splice_Rec_1008903,Human_Splice_Rec_1008905 RMVar_hsa_circ_76158,RMVar_hsa_circ_111351,RMVar_hsa_circ_254315,RMVar_hsa_circ_254316 71599 RMVar_ID_71599 Human_SNP_ID_381815477 m1A Human chr8 - 127737445 127737445 127737445 CACCAAGGGTAGCAGCTGTTCTGGAACCGCCCAGAGCCCCGCTCCTCGCAGTTCCTCCGCATCTC CACCAAGGGTAGCAGCTGTTCTGGAACCGCCCGGAGCCCCGCTCCTCGCAGTTCCTCCGCATCTC T C CASC11 Ensembl:ENSG00000249375 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:127737443..127737546 26863196 MeRIP-seq:(Medium) rs901689056 Functional Loss SNV dbSNP153 33..33 33 - - - 71600 RMVar_ID_71600 Human_SNP_ID_381815538 m1A Human chr8 + 127737642 127737642 127737642 CTGAGCTCGCCACTCCAGCCGGCGAGAGAAAGAAGAAAAGCTGGCAAAAGGAGTGTTGGACGGGG CTGAGCTCGCCACTCCAGCCGGCGAGAGAAAGGAGAAAAGCTGGCAAAAGGAGTGTTGGACGGGG A G MYC Ensembl:ENSG00000136997 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127737636..127737766 26863196 MeRIP-seq:(Medium) rs376532664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1008909 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316 71601 RMVar_ID_71601 Human_SNP_ID_381815539 m1A Human chr8 + 127737642 127737642 127737642 CTGAGCTCGCCACTCCAGCCGGCGAGAGAAAGAAGAAAAGCTGGCAAAAGGAGTGTTGGACGGGG CTGAGCTCGCCACTCCAGCCGGCGAGAGAAAGTAGAAAAGCTGGCAAAAGGAGTGTTGGACGGGG A T MYC Ensembl:ENSG00000136997 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127737636..127737766 26863196 MeRIP-seq:(Medium) rs376532664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1008909 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316 71602 RMVar_ID_71602 Human_SNP_ID_381815593 m1A Human chr8 + 127737750 127737750 127737750 GGGAGGGGCTGCGGTGCCGGCGGGGGTAGGAGAGCGGCTAGGGCGCGAGTGGGAACAGCCGCAGC GGGAGGGGCTGCGGTGCCGGCGGGGGTAGGAGCGCGGCTAGGGCGCGAGTGGGAACAGCCGCAGC A C MYC Ensembl:ENSG00000136997 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127737747..127737851 26863196 MeRIP-seq:(Medium) rs1463865822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795211,Human_RBP_ID_845108,Human_RBP_ID_960484,Human_RBP_ID_1070334,Human_RBP_ID_3885380,Human_RBP_ID_3973331,Human_RBP_ID_5154114,Human_RBP_ID_5224209,Human_RBP_ID_5328915,Human_RBP_ID_5405461,Human_RBP_ID_5658302,Human_RBP_ID_8154743,Human_RBP_ID_8221183,Human_RBP_ID_8238574,Human_RBP_ID_8944545,Human_RBP_ID_9338367,Human_RBP_ID_9351673,Human_RBP_ID_9440747,Human_RBP_ID_18427113,Human_RBP_ID_18466815,Human_RBP_ID_18961087,Human_RBP_ID_22115549,Human_RBP_ID_22419306,Human_RBP_ID_22555531,Human_RBP_ID_22688493,Human_RBP_ID_22731579,Human_RBP_ID_23259428,Human_RBP_ID_23299309,Human_RBP_ID_26360151,Human_RBP_ID_26772371,Human_RBP_ID_26795126 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316 71603 RMVar_ID_71603 Human_SNP_ID_381815827 m1A Human chr8 - 127738426 127738423 127738426 GGCGGCTAGGGGACAGGGGCGGGGTGGGCAGCAGCTCGAATTTCTTCCAGATATCCTCGCTGGGC GGCGGCTAGGGGACAGGGGCGGGGTGGGCAGC___TCGAATTTCTTCCAGATATCCTCGCTGGGC AGCT A CASC11 Ensembl:ENSG00000249375 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:127738376..127738425 26863196 MeRIP-seq:(Medium) rs769788275 Functional Loss DEL dbSNP153 33..35 33 - - - 71604 RMVar_ID_71604 Human_SNP_ID_381816026 m1A Human chr8 + 127738902 127738902 127738902 GCTCGCCCAAGTCCTGCGCCTCGCAAGACTCCAGCGCCTTCTCTCCGTCCTCGGATTCTCTGCTC GCTCGCCCAAGTCCTGCGCCTCGCAAGACTCCCGCGCCTTCTCTCCGTCCTCGGATTCTCTGCTC A C MYC Ensembl:ENSG00000136997 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr8:127738651..127739125;chr8:127738854..127739025 26863196 MeRIP-seq:(Medium) rs1166344892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4997951,Human_RBP_ID_16352756,Human_RBP_ID_22534423,Human_RBP_ID_27161868,Human_RBP_ID_27535951 Human_miRNA_ID_2134955,Human_miRNA_ID_2136453,Human_miRNA_ID_2609107,Human_miRNA_ID_2665248,Human_miRNA_ID_2854459,Human_miRNA_ID_2857138 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 71605 RMVar_ID_71605 Human_SNP_ID_381816562 m1A Human chr8 - 127740601 127740601 127740601 ACTCTGACACTGTCCAACTTGACCCTCTTGGCAGCAGGATAGTCCTTCCGAGTGGAGGGAGGCGC ACTCTGACACTGTCCAACTTGACCCTCTTGGCTGCAGGATAGTCCTTCCGAGTGGAGGGAGGCGC T A lnc-FAM84B-20 RNACentral:URS0000D5E1FC lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:127740551..127740625 32194978 MeRIP-seq:(Medium) rs1380596446 Functional Loss SNV dbSNP153 33..33 33 - - - 71606 RMVar_ID_71606 Human_SNP_ID_381816563 m1A Human chr8 - 127740601 127740601 127740601 ACTCTGACACTGTCCAACTTGACCCTCTTGGCAGCAGGATAGTCCTTCCGAGTGGAGGGAGGCGC ACTCTGACACTGTCCAACTTGACCCTCTTGGCGGCAGGATAGTCCTTCCGAGTGGAGGGAGGCGC T C lnc-FAM84B-20 RNACentral:URS0000D5E1FC lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:127740551..127740625 32194978 MeRIP-seq:(Medium) rs1380596446 Functional Loss SNV dbSNP153 33..33 33 - - - 71607 RMVar_ID_71607 Human_SNP_ID_381816675 m1A Human chr8 + 127740963 127740954 127740964 TGAACAGCTACGGAACTCTTGTGCGTAAGGAAAAGTAAGGAAAACGATTCCTTCTAACAGAAATG TGAACAGCTACGGAACTCTTGTGC__________GTAAGGAAAACGATTCCTTCTAACAGAAATG CGTAAGGAAAA C MYC Ensembl:ENSG00000136997 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1327994073 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_88462,Human_RBP_ID_3140078,Human_RBP_ID_4970924,Human_RBP_ID_9405785,Human_RBP_ID_17319620,Human_RBP_ID_22115757,Human_RBP_ID_22516619,Human_RBP_ID_24245452,Human_RBP_ID_24549423,Human_RBP_ID_27120859 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 71608 RMVar_ID_71608 Human_SNP_ID_381816681 m1A Human chr8 + 127740963 127740963 127740963 TGAACAGCTACGGAACTCTTGTGCGTAAGGAAAAGTAAGGAAAACGATTCCTTCTAACAGAAATG TGAACAGCTACGGAACTCTTGTGCGTAAGGAACAGTAAGGAAAACGATTCCTTCTAACAGAAATG A C MYC Ensembl:ENSG00000136997 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs779751378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88462,Human_RBP_ID_3140078,Human_RBP_ID_4970924,Human_RBP_ID_9405785,Human_RBP_ID_17319620,Human_RBP_ID_22115757,Human_RBP_ID_22516619,Human_RBP_ID_24245452,Human_RBP_ID_24549423,Human_RBP_ID_27120859 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 71609 RMVar_ID_71609 Human_SNP_ID_381816682 m1A Human chr8 + 127740963 127740963 127740963 TGAACAGCTACGGAACTCTTGTGCGTAAGGAAAAGTAAGGAAAACGATTCCTTCTAACAGAAATG TGAACAGCTACGGAACTCTTGTGCGTAAGGAAGAGTAAGGAAAACGATTCCTTCTAACAGAAATG A G MYC Ensembl:ENSG00000136997 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs779751378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88462,Human_RBP_ID_3140078,Human_RBP_ID_4970924,Human_RBP_ID_9405785,Human_RBP_ID_17319620,Human_RBP_ID_22115757,Human_RBP_ID_22516619,Human_RBP_ID_24245452,Human_RBP_ID_24549423,Human_RBP_ID_27120859 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 71610 RMVar_ID_71610 Human_SNP_ID_381831526 m1A Human chr8 + 127794602 127794602 127794602 CCCGCGGGCCGGGCGGGCTCGGGGCGGCCGGGACGAGGAGGGGCGACGACGAGCTGCGAGCAAAG CCCGCGGGCCGGGCGGGCTCGGGGCGGCCGGGTCGAGGAGGGGCGACGACGAGCTGCGAGCAAAG A T PVT1 Ensembl:ENSG00000249859 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127794552..127794693 26863196 MeRIP-seq:(Medium) rs1202952257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3888289,Human_RBP_ID_5628637,Human_RBP_ID_8274267,Human_RBP_ID_18426749,Human_RBP_ID_23117142,Human_RBP_ID_26359367 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 71611 RMVar_ID_71611 Human_SNP_ID_381833522 m1A Human chr8 - 127802783 127802783 127802783 CATCTGCAGTGTGCCTCCCTCCCACACTGGAAACTTCCCGAAGATGGCAACGGTTTCTCATTCAC CATCTGCAGTGTGCCTCCCTCCCACACTGGAAGCTTCCCGAAGATGGCAACGGTTTCTCATTCAC T C lnc-FAM84B-8 RNACentral:URS00008BDA4B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127802739..127802828 26863196 MeRIP-seq:(Medium) rs4410871 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8731,GWAS_ID_8732,GWAS_ID_8733,GWAS_ID_8734,GWAS_ID_8735,GWAS_ID_8736,GWAS_ID_8737 71612 RMVar_ID_71612 Human_SNP_ID_381833531 m1A Human chr8 + 127802806 127802806 127802806 TTCGGGAAGTTTCCAGTGTGGGAGGGAGGCACACTGCAGATGTAACTGCTAGGAGAGAAAGAAGG TTCGGGAAGTTTCCAGTGTGGGAGGGAGGCACGCTGCAGATGTAACTGCTAGGAGAGAAAGAAGG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:127802800..127803050 26863196 MeRIP-seq:(Medium) rs1210704718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5632614,Human_RBP_ID_16353190 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 71613 RMVar_ID_71613 Human_SNP_ID_381835050 m1A Human chr8 - 127808582 127808582 127808582 GATCCACCATCTACCCAACAAAAAGGTCAATCAAATCAGGAACCACCCAGCTTAGCCACCCCCAA GATCCACCATCTACCCAACAAAAAGGTCAATCGAATCAGGAACCACCCAGCTTAGCCACCCCCAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127808553..127808704 26863196 MeRIP-seq:(Medium) rs1317945315 Functional Loss SNV dbSNP153 33..33 33 - - - 71614 RMVar_ID_71614 Human_SNP_ID_381835051 m1A Human chr8 - 127808582 127808582 127808582 GATCCACCATCTACCCAACAAAAAGGTCAATCAAATCAGGAACCACCCAGCTTAGCCACCCCCAA GATCCACCATCTACCCAACAAAAAGGTCAATCCAATCAGGAACCACCCAGCTTAGCCACCCCCAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127808553..127808704 26863196 MeRIP-seq:(Medium) rs1317945315 Functional Loss SNV dbSNP153 33..33 33 - - - 71615 RMVar_ID_71615 Human_SNP_ID_381836072 m1A Human chr8 + 127812313 127812313 127812313 AGGAAGGAAGAGAATGAAAGGCTGGGCGTGGTAGCTCTTGCCTGTTGTAGTCCTGGCACTTTGGG AGGAAGGAAGAGAATGAAAGGCTGGGCGTGGTGGCTCTTGCCTGTTGTAGTCCTGGCACTTTGGG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127812264..127812356 26863196 MeRIP-seq:(Medium) rs1394019685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8680489,Human_RBP_ID_24391945 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 71616 RMVar_ID_71616 Human_SNP_ID_381836078 m1A Human chr8 - 127812334 127812334 127812334 CAATTCCTCCCATCTCAGCCTCCCAAAGTGCCAGGACTACAACAGGCAAGAGCTACCACGCCCAG CAATTCCTCCCATCTCAGCCTCCCAAAGTGCCGGGACTACAACAGGCAAGAGCTACCACGCCCAG T C lnc-FAM84B-7 RNACentral:URS00008B8F1D lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127812218..127812768 26863196 MeRIP-seq:(Medium) rs896027539 Functional Loss SNV dbSNP153 33..33 33 - - - 71617 RMVar_ID_71617 Human_SNP_ID_381841044 m1A Human chr8 - 127831554 127831554 127831554 TATGTCCACTTTTCTATCTATACTCCACTCCCATGGATTTGGATCCCACCTCTGCCAAAATCTTC TATGTCCACTTTTCTATCTATACTCCACTCCCGTGGATTTGGATCCCACCTCTGCCAAAATCTTC T C lnc-FAM84B-7 RNACentral:URS00008B8F1D lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127831544..127831750 26863196 MeRIP-seq:(Medium) rs368303900 Functional Loss SNV dbSNP153 33..33 33 - - - 71618 RMVar_ID_71618 Human_SNP_ID_381849348 m1A Human chr8 + 127864180 127864180 127864180 TGTGGTTTGCAGTGGGGGTGGGGCAGGAAAGAAAGGTTACGTGGGGTGAAGGGGTCAGGTCAATT TGTGGTTTGCAGTGGGGGTGGGGCAGGAAAGACAGGTTACGTGGGGTGAAGGGGTCAGGTCAATT A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:127864173..127864298 26863196 MeRIP-seq:(Medium) rs902170995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9440751,Human_RBP_ID_16354710 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_104807,RMVar_hsa_circ_254321,RMVar_hsa_circ_254322 71619 RMVar_ID_71619 Human_SNP_ID_381857732 m1A Human chr8 + 127897618 127897618 127897618 AAGAGAGGGAGAGGAAGGAAGGAAGAAAGGAAAGAAAGAAAGAAAGACAGACAAAGAAAGAAAGA AAGAGAGGGAGAGGAAGGAAGGAAGAAAGGAAGGAAAGAAAGAAAGACAGACAAAGAAAGAAAGA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:127897524..127897694 26863196 MeRIP-seq:(Medium) rs1183476007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3140711,Human_RBP_ID_5105790 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_254326,RMVar_hsa_circ_254322,RMVar_hsa_circ_308246,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_83584,RMVar_hsa_circ_254327,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_254323 71620 RMVar_ID_71620 Human_SNP_ID_381857868 m1A Human chr8 + 127897896 127897896 127897896 AAGAAAGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAAAAGACAGACAGGAAGGAAGAAAGG AAGAAAGGAAAGAAAGAAAGAAAGAAAGAAAGGAAGAAAAAAAGACAGACAGGAAGGAAGAAAGG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127897846..127897938 26863196 MeRIP-seq:(Medium) rs1282934924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105790,Human_RBP_ID_26152519 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_254326,RMVar_hsa_circ_254322,RMVar_hsa_circ_308246,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_83584,RMVar_hsa_circ_254327,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_254323 71621 RMVar_ID_71621 Human_SNP_ID_381858636 m1A Human chr8 + 127901113 127901113 127901113 AAGACATTGCTGTTGAGAAGATACTTGTGAAGAAGCCAACAGCGTTGTCTGGGCCTGGCTGGATA AAGACATTGCTGTTGAGAAGATACTTGTGAAGCAGCCAACAGCGTTGTCTGGGCCTGGCTGGATA A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:127901107..127901203 26863196 MeRIP-seq:(Medium) rs988103297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3888798,Human_RBP_ID_16355178 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_254326,RMVar_hsa_circ_254322,RMVar_hsa_circ_308246,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_83584,RMVar_hsa_circ_254327,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_254323 71622 RMVar_ID_71622 Human_SNP_ID_381858637 m1A Human chr8 + 127901113 127901113 127901113 AAGACATTGCTGTTGAGAAGATACTTGTGAAGAAGCCAACAGCGTTGTCTGGGCCTGGCTGGATA AAGACATTGCTGTTGAGAAGATACTTGTGAAGGAGCCAACAGCGTTGTCTGGGCCTGGCTGGATA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:127901107..127901203 26863196 MeRIP-seq:(Medium) rs988103297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3888798,Human_RBP_ID_16355178 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_254326,RMVar_hsa_circ_254322,RMVar_hsa_circ_308246,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_83584,RMVar_hsa_circ_254327,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_254323 71623 RMVar_ID_71623 Human_SNP_ID_381867276 m1A Human chr8 - 127935897 127935897 127935897 TTTGGGCCACACCACCCACTGACACCTCTCAGATCAGGAAGCTACCAGTTACTCCAGCTTTTGGC TTTGGGCCACACCACCCACTGACACCTCTCAGGTCAGGAAGCTACCAGTTACTCCAGCTTTTGGC T C lnc-FAM84B-7 RNACentral:URS00008B8F1D lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127935859..127935952 26863196 MeRIP-seq:(Medium) rs889989109 Functional Loss SNV dbSNP153 33..33 33 - - - 71624 RMVar_ID_71624 Human_SNP_ID_381908065 m1A Human chr8 - 128101114 128101114 128101114 TTTGGGGGAAGGGGTGGGGGTGGACAGGTAACAGGTGCTTGCTGCTGAGTGGTTGGGGCAGAGAT TTTGGGGGAAGGGGTGGGGGTGGACAGGTAACCGGTGCTTGCTGCTGAGTGGTTGGGGCAGAGAT T G lnc-FAM84B-7 RNACentral:URS00008B8F1D lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:128101064..128101162 26863196 MeRIP-seq:(Medium) rs1177998744 Functional Loss SNV dbSNP153 33..33 33 - - - 71625 RMVar_ID_71625 Human_SNP_ID_382362965 m1A Human chr8 - 129885888 129885888 129885888 ACAGTGAGGTCATTTCCTGCAAGTGAGAATGGAGGATGGGTTGTTGGGTTTTTGTGGTTTTCTTC ACAGTGAGGTCATTTCCTGCAAGTGAGAATGGGGGATGGGTTGTTGGGTTTTTGTGGTTTTCTTC T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:129885886..129886128 26863196 MeRIP-seq:(Medium) rs1346277637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7813080 RMVar_hsa_circ_349114,RMVar_hsa_circ_21312,RMVar_hsa_circ_254350,RMVar_hsa_circ_78826,RMVar_hsa_circ_254352,RMVar_hsa_circ_288393,RMVar_hsa_circ_371735,RMVar_hsa_circ_254353,RMVar_hsa_circ_254354,RMVar_hsa_circ_324701,RMVar_hsa_circ_254359,RMVar_hsa_circ_254362,RMVar_hsa_circ_317694,RMVar_hsa_circ_293972,RMVar_hsa_circ_254361,RMVar_hsa_circ_47370,RMVar_hsa_circ_290662,RMVar_hsa_circ_254363,RMVar_hsa_circ_254364 71626 RMVar_ID_71626 Human_SNP_ID_382363130 m1A Human chr8 - 129886661 129886661 129886661 GACACTGGAATTAGCAACGTGGAAGTTACCTGATGGCCTTCCCAGTGCAGTTTTGGTGGTGTGGG GACACTGGAATTAGCAACGTGGAAGTTACCTGTTGGCCTTCCCAGTGCAGTTTTGGTGGTGTGGG T A CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:129886657..129886928 26863196 MeRIP-seq:(Medium) rs191110504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349114,RMVar_hsa_circ_21312,RMVar_hsa_circ_254350,RMVar_hsa_circ_78826,RMVar_hsa_circ_254352,RMVar_hsa_circ_288393,RMVar_hsa_circ_371735,RMVar_hsa_circ_254353,RMVar_hsa_circ_254354,RMVar_hsa_circ_324701,RMVar_hsa_circ_254359,RMVar_hsa_circ_254362,RMVar_hsa_circ_317694,RMVar_hsa_circ_293972,RMVar_hsa_circ_254361,RMVar_hsa_circ_47370,RMVar_hsa_circ_290662,RMVar_hsa_circ_254363,RMVar_hsa_circ_254364 71627 RMVar_ID_71627 Human_SNP_ID_382363545 m1A Human chr8 - 129888462 129888462 129888462 GTGTGCAGTGGAGAGTAAAGAAAGATGAGGCCAGAGTGTGTCGGAGCAGATTGTGTAAGATTTTG GTGTGCAGTGGAGAGTAAAGAAAGATGAGGCCGGAGTGTGTCGGAGCAGATTGTGTAAGATTTTG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:129888460..129888619 26863196 MeRIP-seq:(Medium) rs1322901193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16361121,Human_RBP_ID_24246181 RMVar_hsa_circ_349114,RMVar_hsa_circ_21312,RMVar_hsa_circ_254350,RMVar_hsa_circ_78826,RMVar_hsa_circ_254352,RMVar_hsa_circ_288393,RMVar_hsa_circ_371735,RMVar_hsa_circ_254353,RMVar_hsa_circ_254354,RMVar_hsa_circ_324701,RMVar_hsa_circ_254359,RMVar_hsa_circ_254362,RMVar_hsa_circ_317694,RMVar_hsa_circ_293972,RMVar_hsa_circ_254361,RMVar_hsa_circ_47370,RMVar_hsa_circ_290662,RMVar_hsa_circ_254363,RMVar_hsa_circ_254364 71628 RMVar_ID_71628 Human_SNP_ID_382376009 m1A Human chr8 + 129939625 129939625 129939625 AAACCAATCACTCACCCTCCGCTCGAGCCTCCAGGCGCTCTCAGTCCCGCTCCTGCGCCCTCCTG AAACCAATCACTCACCCTCCGCTCGAGCCTCCCGGCGCTCTCAGTCCCGCTCCTGCGCCCTCCTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:129939622..129939791 26863196 MeRIP-seq:(Medium) rs1169269598 Functional Loss SNV dbSNP153 33..33 33 - - - 71629 RMVar_ID_71629 Human_SNP_ID_382387293 m1A Human chr8 - 129987422 129987422 129987422 GGGGACTTAGCTCAGCCTCCCAGGTGCCATCAACAAGCCACAGTCAGACCCGAAATGGTAGCCAG GGGGACTTAGCTCAGCCTCCCAGGTGCCATCAGCAAGCCACAGTCAGACCCGAAATGGTAGCCAG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:129987417..129987528 26863196 MeRIP-seq:(Medium) rs896872879 Functional Loss SNV dbSNP153 33..33 33 - - - 71630 RMVar_ID_71630 Human_SNP_ID_382394740 m1A Human chr8 + 130016137 130016137 130016137 CTCGCGTCCGCCCGCCGCCCCCCGCGCACTCGAGGCGCCTCCCCCGGGACCCCCGCGCCCGCCGG CTCGCGTCCGCCCGCCGCCCCCCGCGCACTCGGGGCGCCTCCCCCGGGACCCCCGCGCCCGCCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:130016091..130016230 26863196 MeRIP-seq:(Medium) rs959509756 Functional Loss SNV dbSNP153 33..33 33 - - - 71631 RMVar_ID_71631 Human_SNP_ID_382406813 m1A Human chr8 - 130060888 130060888 130060888 CAAATTGGAGATTTGCCGCCTAAGCCAGGAGAACTGCCCCCCAAACCACAGCTGGGGGACCTGCC CAAATTGGAGATTTGCCGCCTAAGCCAGGAGAGCTGCCCCCCAAACCACAGCTGGGGGACCTGCC T C ASAP1 Ensembl:ENSG00000153317 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:130060837..130061025 26863196 MeRIP-seq:(Medium) rs1564914521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17320318,Human_RBP_ID_17434226 Human_miRNA_ID_1014161,Human_miRNA_ID_1022314,Human_miRNA_ID_1296167,Human_miRNA_ID_1300104 RMVar_hsa_circ_8573,RMVar_hsa_circ_29591,RMVar_hsa_circ_108968,RMVar_hsa_circ_77940,RMVar_hsa_circ_365334,RMVar_hsa_circ_254369,RMVar_hsa_circ_268041,RMVar_hsa_circ_40602,RMVar_hsa_circ_21391,RMVar_hsa_circ_118843,RMVar_hsa_circ_254370,RMVar_hsa_circ_4503,RMVar_hsa_circ_269502,RMVar_hsa_circ_49383,RMVar_hsa_circ_14676,RMVar_hsa_circ_254371 71632 RMVar_ID_71632 Human_SNP_ID_382415481 m1A Human chr8 - 130092084 130092084 130092084 CTCTAAGCACCCAGACCTCTAGTGGCAGCTCCACCCTATCCAAGAAGAGGCCTCCTCCCCCACCA CTCTAAGCACCCAGACCTCTAGTGGCAGCTCCCCCCTATCCAAGAAGAGGCCTCCTCCCCCACCA T G ASAP1 Ensembl:ENSG00000153317 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:130092033..130092174 26863196 MeRIP-seq:(Medium) rs774721997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17434227 Human_Splice_Rec_1011576,Human_Splice_Rec_1011634,Human_Splice_Rec_1011694,Human_Splice_Rec_1011752,Human_Splice_Rec_1011784 Human_miRNA_ID_1271948 RMVar_hsa_circ_12251,RMVar_hsa_circ_29591,RMVar_hsa_circ_108968,RMVar_hsa_circ_77940,RMVar_hsa_circ_254369,RMVar_hsa_circ_268041,RMVar_hsa_circ_40602,RMVar_hsa_circ_118843,RMVar_hsa_circ_254370,RMVar_hsa_circ_4503,RMVar_hsa_circ_269502,RMVar_hsa_circ_49383,RMVar_hsa_circ_14676,RMVar_hsa_circ_114118,RMVar_hsa_circ_323019,RMVar_hsa_circ_342441,RMVar_hsa_circ_254371,RMVar_hsa_circ_374776,RMVar_hsa_circ_323361,RMVar_hsa_circ_99240,RMVar_hsa_circ_254374,RMVar_hsa_circ_254375,RMVar_hsa_circ_254373,RMVar_hsa_circ_254377,RMVar_hsa_circ_111436,RMVar_hsa_circ_281873,RMVar_hsa_circ_368116,RMVar_hsa_circ_266396,RMVar_hsa_circ_254378,RMVar_hsa_circ_340844,RMVar_hsa_circ_254376,RMVar_hsa_circ_352851,RMVar_hsa_circ_325876,RMVar_hsa_circ_40305,RMVar_hsa_circ_57592,RMVar_hsa_circ_23508,RMVar_hsa_circ_254379 71633 RMVar_ID_71633 Human_SNP_ID_382420825 m1A Human chr8 + 130112142 130112142 130112142 AGGAGGCAGAGGGGGAGCCTCCGTGGTTGGTGATGTGGGCGAGTCTGTGCTTGTGGAAACGAAGA AGGAGGCAGAGGGGGAGCCTCCGTGGTTGGTGCTGTGGGCGAGTCTGTGCTTGTGGAAACGAAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:130112069..130112243 26863196 MeRIP-seq:(Medium) rs543968964 Functional Loss SNV dbSNP153 33..33 33 - - - 71634 RMVar_ID_71634 Human_SNP_ID_382420858 m1A Human chr8 - 130112218 130112218 130112218 GACAAGCTGGCACTGCCAGGATTCAGCACTCCAAGGGACAAACAGCGGCTCTCCTATGGAGCCTT GACAAGCTGGCACTGCCAGGATTCAGCACTCCCAGGGACAAACAGCGGCTCTCCTATGGAGCCTT T G ASAP1 Ensembl:ENSG00000153317 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:130112169..130112253 26863196 MeRIP-seq:(Medium) rs200323716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17320319 Human_miRNA_ID_97148,Human_miRNA_ID_429653,Human_miRNA_ID_1263646,Human_miRNA_ID_1271949,Human_miRNA_ID_1341355,Human_miRNA_ID_2615187 RMVar_hsa_circ_12251,RMVar_hsa_circ_108968,RMVar_hsa_circ_77940,RMVar_hsa_circ_254369,RMVar_hsa_circ_268041,RMVar_hsa_circ_40602,RMVar_hsa_circ_118843,RMVar_hsa_circ_254370,RMVar_hsa_circ_4503,RMVar_hsa_circ_269502,RMVar_hsa_circ_49383,RMVar_hsa_circ_114118,RMVar_hsa_circ_342441,RMVar_hsa_circ_254371,RMVar_hsa_circ_374776,RMVar_hsa_circ_323361,RMVar_hsa_circ_99240,RMVar_hsa_circ_254374,RMVar_hsa_circ_254375,RMVar_hsa_circ_254377,RMVar_hsa_circ_111436,RMVar_hsa_circ_368116,RMVar_hsa_circ_266396,RMVar_hsa_circ_254376,RMVar_hsa_circ_352851,RMVar_hsa_circ_325876,RMVar_hsa_circ_40305,RMVar_hsa_circ_57592,RMVar_hsa_circ_23508,RMVar_hsa_circ_7366,RMVar_hsa_circ_92693,RMVar_hsa_circ_309777,RMVar_hsa_circ_344314,RMVar_hsa_circ_360483,RMVar_hsa_circ_254379,RMVar_hsa_circ_346755,RMVar_hsa_circ_343869,RMVar_hsa_circ_275983,RMVar_hsa_circ_86048,RMVar_hsa_circ_88936,RMVar_hsa_circ_35681,RMVar_hsa_circ_254380,RMVar_hsa_circ_254382,RMVar_hsa_circ_254383,RMVar_hsa_circ_254384,RMVar_hsa_circ_254381 71635 RMVar_ID_71635 Human_SNP_ID_382443283 m1A Human chr8 - 130198931 130198931 130198931 GGAGTTGTAGTGCAGTGAGAATGGGTAGAGGGACTCAAAACAGGTTGGCAGGGCCAGAGCTAAAT GGAGTTGTAGTGCAGTGAGAATGGGTAGAGGGCCTCAAAACAGGTTGGCAGGGCCAGAGCTAAAT T G ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:130198930..130199013 26863196 MeRIP-seq:(Medium) rs1260651762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16363188 RMVar_hsa_circ_26835,RMVar_hsa_circ_826,RMVar_hsa_circ_77940,RMVar_hsa_circ_118843,RMVar_hsa_circ_254370,RMVar_hsa_circ_114118,RMVar_hsa_circ_254371,RMVar_hsa_circ_111436,RMVar_hsa_circ_254376,RMVar_hsa_circ_57592,RMVar_hsa_circ_92693,RMVar_hsa_circ_360483,RMVar_hsa_circ_254379,RMVar_hsa_circ_88936,RMVar_hsa_circ_35681,RMVar_hsa_circ_254383,RMVar_hsa_circ_254384,RMVar_hsa_circ_115025,RMVar_hsa_circ_76738,RMVar_hsa_circ_109915,RMVar_hsa_circ_254388,RMVar_hsa_circ_254387,RMVar_hsa_circ_254389,RMVar_hsa_circ_125837,RMVar_hsa_circ_87752,RMVar_hsa_circ_254391,RMVar_hsa_circ_117050,RMVar_hsa_circ_254393,RMVar_hsa_circ_254394,RMVar_hsa_circ_27059,RMVar_hsa_circ_54015,RMVar_hsa_circ_122496,RMVar_hsa_circ_95799,RMVar_hsa_circ_254399,RMVar_hsa_circ_254400,RMVar_hsa_circ_312083,RMVar_hsa_circ_354780,RMVar_hsa_circ_374795,RMVar_hsa_circ_87937,RMVar_hsa_circ_119862,RMVar_hsa_circ_35465,RMVar_hsa_circ_254410,RMVar_hsa_circ_254411,RMVar_hsa_circ_254409,RMVar_hsa_circ_352363,RMVar_hsa_circ_283052,RMVar_hsa_circ_306382,RMVar_hsa_circ_254422,RMVar_hsa_circ_14087,RMVar_hsa_circ_254423,RMVar_hsa_circ_322533,RMVar_hsa_circ_340930,RMVar_hsa_circ_295523,RMVar_hsa_circ_254430,RMVar_hsa_circ_254431,RMVar_hsa_circ_87768,RMVar_hsa_circ_321010,RMVar_hsa_circ_254434,RMVar_hsa_circ_336221,RMVar_hsa_circ_254432,RMVar_hsa_circ_254433,RMVar_hsa_circ_367861,RMVar_hsa_circ_367979,RMVar_hsa_circ_31200,RMVar_hsa_circ_254435,RMVar_hsa_circ_254437,RMVar_hsa_circ_334372,RMVar_hsa_circ_351942,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438 71636 RMVar_ID_71636 Human_SNP_ID_382468147 m1A Human chr8 + 130298707 130298707 130298707 TTAGCTATAACATACATCTTTTACTTCCTCAAAAGTGGCAGGTTCTCTCCCACCTCTATCCCTCT TTAGCTATAACATACATCTTTTACTTCCTCAACAGTGGCAGGTTCTCTCCCACCTCTATCCCTCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:130298705..130298817 26863196 MeRIP-seq:(Medium) rs1008668588 Functional Loss SNV dbSNP153 33..33 33 - - - 71637 RMVar_ID_71637 Human_SNP_ID_382482949 m1A Human chr8 - 130358423 130358423 130358423 TCCCCCGCCGCTGAGGAGCTGCCGCCGCCGGCATGAGCAGAGGGAGGCGGGTCCCGGAGAGCCCC TCCCCCGCCGCTGAGGAGCTGCCGCCGCCGGCGTGAGCAGAGGGAGGCGGGTCCCGGAGAGCCCC T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:130358422..130358535 32194978 MeRIP-seq:(Medium) rs1448490897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974098,Human_RBP_ID_9338376,Human_RBP_ID_26359376,Human_RBP_ID_27831574 RMVar_hsa_circ_114118,RMVar_hsa_circ_92693,RMVar_hsa_circ_254379,RMVar_hsa_circ_88936,RMVar_hsa_circ_254383,RMVar_hsa_circ_254384,RMVar_hsa_circ_76738,RMVar_hsa_circ_254388,RMVar_hsa_circ_125837,RMVar_hsa_circ_254391,RMVar_hsa_circ_117050,RMVar_hsa_circ_254394,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_119862,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_254422,RMVar_hsa_circ_111342,RMVar_hsa_circ_31200,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_277578,RMVar_hsa_circ_312193,RMVar_hsa_circ_254442,RMVar_hsa_circ_77337,RMVar_hsa_circ_328571,RMVar_hsa_circ_306600,RMVar_hsa_circ_254444,RMVar_hsa_circ_76417,RMVar_hsa_circ_254448,RMVar_hsa_circ_273928,RMVar_hsa_circ_254450,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254456,RMVar_hsa_circ_96745,RMVar_hsa_circ_254457,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451 71638 RMVar_ID_71638 Human_SNP_ID_382482950 m1A Human chr8 - 130358423 130358423 130358423 TCCCCCGCCGCTGAGGAGCTGCCGCCGCCGGCATGAGCAGAGGGAGGCGGGTCCCGGAGAGCCCC TCCCCCGCCGCTGAGGAGCTGCCGCCGCCGGCCTGAGCAGAGGGAGGCGGGTCCCGGAGAGCCCC T G ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:130358422..130358535 32194978 MeRIP-seq:(Medium) rs1448490897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974098,Human_RBP_ID_9338376,Human_RBP_ID_26359376,Human_RBP_ID_27831574 RMVar_hsa_circ_114118,RMVar_hsa_circ_92693,RMVar_hsa_circ_254379,RMVar_hsa_circ_88936,RMVar_hsa_circ_254383,RMVar_hsa_circ_254384,RMVar_hsa_circ_76738,RMVar_hsa_circ_254388,RMVar_hsa_circ_125837,RMVar_hsa_circ_254391,RMVar_hsa_circ_117050,RMVar_hsa_circ_254394,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_119862,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_254422,RMVar_hsa_circ_111342,RMVar_hsa_circ_31200,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_277578,RMVar_hsa_circ_312193,RMVar_hsa_circ_254442,RMVar_hsa_circ_77337,RMVar_hsa_circ_328571,RMVar_hsa_circ_306600,RMVar_hsa_circ_254444,RMVar_hsa_circ_76417,RMVar_hsa_circ_254448,RMVar_hsa_circ_273928,RMVar_hsa_circ_254450,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254456,RMVar_hsa_circ_96745,RMVar_hsa_circ_254457,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451 71639 RMVar_ID_71639 Human_SNP_ID_382482969 m1A Human chr8 + 130358455 130358455 130358455 TGCCGGCGGCGGCAGCTCCTCAGCGGCGGGGGAGGGGACGCGGCTGCGCGCGGGGTCTTCGCGGG TGCCGGCGGCGGCAGCTCCTCAGCGGCGGGGGGGGGGACGCGGCTGCGCGCGGGGTCTTCGCGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:130358156..130358595 26863196 MeRIP-seq:(Medium) rs995858267 Functional Loss SNV dbSNP153 33..33 33 - - - 71640 RMVar_ID_71640 Human_SNP_ID_382482986 m1A Human chr8 - 130358490 130358490 130358490 CGCGCACGCCCCAGCGGCCGGCCGGAGCCCAGACCCCCGCGAAGACCCCGCGCGCAGCCGCGTCC CGCGCACGCCCCAGCGGCCGGCCGGAGCCCAGCCCCCCGCGAAGACCCCGCGCGCAGCCGCGTCC T G ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:130358415..130358541 26863196 MeRIP-seq:(Medium) rs983545043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22534424,Human_RBP_ID_26795559 RMVar_hsa_circ_114118,RMVar_hsa_circ_92693,RMVar_hsa_circ_254379,RMVar_hsa_circ_88936,RMVar_hsa_circ_254383,RMVar_hsa_circ_254384,RMVar_hsa_circ_76738,RMVar_hsa_circ_254388,RMVar_hsa_circ_125837,RMVar_hsa_circ_254391,RMVar_hsa_circ_117050,RMVar_hsa_circ_254394,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_119862,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_254422,RMVar_hsa_circ_111342,RMVar_hsa_circ_31200,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_277578,RMVar_hsa_circ_312193,RMVar_hsa_circ_254442,RMVar_hsa_circ_77337,RMVar_hsa_circ_328571,RMVar_hsa_circ_306600,RMVar_hsa_circ_254444,RMVar_hsa_circ_76417,RMVar_hsa_circ_254448,RMVar_hsa_circ_273928,RMVar_hsa_circ_254450,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254456,RMVar_hsa_circ_96745,RMVar_hsa_circ_254457,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451 71641 RMVar_ID_71641 Human_SNP_ID_382498617 m1A Human chr8 - 130422407 130422407 130422407 TGATCCGAGCCTGGGAATTTACTTTTCTATCAAGGAATTAGAAAGTCAGGCCTCATCTGGAAAGG TGATCCGAGCCTGGGAATTTACTTTTCTATCAGGGAATTAGAAAGTCAGGCCTCATCTGGAAAGG T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:130422405..130422556 26863196 MeRIP-seq:(Medium) rs147270807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3142403,Human_RBP_ID_16364924 RMVar_hsa_circ_116691,RMVar_hsa_circ_101120,RMVar_hsa_circ_254452,RMVar_hsa_circ_254451,RMVar_hsa_circ_98165,RMVar_hsa_circ_254460,RMVar_hsa_circ_90905,RMVar_hsa_circ_254459 71642 RMVar_ID_71642 Human_SNP_ID_382503921 m1A Human chr8 + 130443543 130443543 130443543 CTCGCGGCTCTCGGGTGGGAAAGCGAACTGCGACCGGGAAGCGCCGGCTGGGCGGGAGGCGCGGG CTCGCGGCTCTCGGGTGGGAAAGCGAACTGCGGCCGGGAAGCGCCGGCTGGGCGGGAGGCGCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:130443494..130443712 26863196 MeRIP-seq:(Medium) rs1235000107 Functional Loss SNV dbSNP153 33..33 33 - - - 71643 RMVar_ID_71643 Human_SNP_ID_382897937 m1A Human chr8 - 131904392 131904392 131904392 GCGCGGCCCAGCCTCCCCAGCCGCCCGGGAGGAGTACCCGGCCCAAGCGCGTCGCGCAGGCAGTC GCGCGGCCCAGCCTCCCCAGCCGCCCGGGAGGCGTACCCGGCCCAAGCGCGTCGCGCAGGCAGTC T G lnc-OC90-2 RNACentral:URS0000D5C490 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:131904342..131904440 26863196 MeRIP-seq:(Medium) rs868414402 Functional Loss SNV dbSNP153 33..33 33 - - - 71644 RMVar_ID_71644 Human_SNP_ID_382906525 m1A Human chr8 - 131940183 131940183 131940183 TTTCTGATGTCATCTGCCCGCAACTCCGGCATACCCCCACCCACCTGTTGCAATCCACTCTACTC TTTCTGATGTCATCTGCCCGCAACTCCGGCATCCCCCCACCCACCTGTTGCAATCCACTCTACTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:131940078..131940198 26863196 MeRIP-seq:(Medium) rs990021034 Functional Loss SNV dbSNP153 33..33 33 - - - 71645 RMVar_ID_71645 Human_SNP_ID_383087398 m1A Human chr8 + 132675433 132675433 132675433 GAGCGGGCGGCGAGGATCCCACGAGACCCGGGACTACTTCCACAAGGGGAACGATCGAGGACGGA GAGCGGGCGGCGAGGATCCCACGAGACCCGGGGCTACTTCCACAAGGGGAACGATCGAGGACGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:132675426..132675526 26863196 MeRIP-seq:(Medium) rs188773730 Functional Loss SNV dbSNP153 33..33 33 - - - 71646 RMVar_ID_71646 Human_SNP_ID_383112776 m1A Human chr8 + 132775406 132775397 132775406 CCCGGCGTCGCGTCAGGGCTGGCCGGCGGCGGAGGCGGCGGCGGCGGCGGCGATGGCAGCGGACC CCCGGCGTCGCGTCAGGGCTGGCC_________GGCGGCGGCGGCGGCGGCGATGGCAGCGGACC CGGCGGCGGA C PHF20L1 Ensembl:ENSG00000129292 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:132775360..132775634;chr8:132775348..132775682 26863196 MeRIP-seq:(Medium) rs1281430778 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4995737,Human_RBP_ID_26359379,Human_RBP_ID_27832170 71647 RMVar_ID_71647 Human_SNP_ID_383112785 m1A Human chr8 + 132775406 132775406 132775406 CCCGGCGTCGCGTCAGGGCTGGCCGGCGGCGGAGGCGGCGGCGGCGGCGGCGATGGCAGCGGACC CCCGGCGTCGCGTCAGGGCTGGCCGGCGGCGGCGGCGGCGGCGGCGGCGGCGATGGCAGCGGACC A C PHF20L1 Ensembl:ENSG00000129292 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:132775360..132775634;chr8:132775348..132775682 26863196 MeRIP-seq:(Medium) rs929400186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995737,Human_RBP_ID_26359379,Human_RBP_ID_27832170 71648 RMVar_ID_71648 Human_SNP_ID_383112831 m1A Human chr8 - 132775472 132775472 132775472 CGCAGCGCCGGATCCGCCCAAGGTTTCGCGGGAGGGAGCTGGGTCCGAGCCCTCAAGCTCGCTCA CGCAGCGCCGGATCCGCCCAAGGTTTCGCGGGCGGGAGCTGGGTCCGAGCCCTCAAGCTCGCTCA T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:132775381..132775476 26863410 MeRIP-seq:(Medium) rs1253256300 Functional Loss SNV dbSNP153 33..33 33 - - - 71649 RMVar_ID_71649 Human_SNP_ID_383230411 m1A Human chr8 - 133237283 133237274 133237283 TGGCCTTGAGTAGAAAAGTCGGGGATCGGGGCAAGAGAGGCTGAGTACGGATGGGAAACTATTGT TGGCCTTGAGTAGAAAAGTCGGGGATCGGGGC_________TGAGTACGGATGGGAAACTATTGT AGCCTCTCTT A NDRG1 Ensembl:ENSG00000104419 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133237176..133237425 32194978 MeRIP-seq:(Medium) rs1311000847 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4971396,Human_RBP_ID_7814709,Human_RBP_ID_8681444,Human_RBP_ID_24247099 RMVar_hsa_circ_122530,RMVar_hsa_circ_89153,RMVar_hsa_circ_254544,RMVar_hsa_circ_254545 71650 RMVar_ID_71650 Human_SNP_ID_383230779 m1A Human chr8 - 133238634 133238634 133238634 CAAGCATCTCCGCATCGCATCCTCTTCCATTAACCAGTGGCCGGTTGCCACTCTCCTCCCCTCCC CAAGCATCTCCGCATCGCATCCTCTTCCATTAGCCAGTGGCCGGTTGCCACTCTCCTCCCCTCCC T C NDRG1 Ensembl:ENSG00000104419 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:133238583..133238665 26863196 MeRIP-seq:(Medium) rs940077482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4971457,Human_RBP_ID_17317143,Human_RBP_ID_17431915,Human_RBP_ID_22775931 RMVar_hsa_circ_89153,RMVar_hsa_circ_254544 71651 RMVar_ID_71651 Human_SNP_ID_383230843 m1A Human chr8 + 133238835 133238835 133238835 GGGGGCGAAAAGGGGCCGGGGAGGAGGGGGCCACTACAGAGATCAGAGTCCGGGGGCGGCAGCTG GGGGGCGAAAAGGGGCCGGGGAGGAGGGGGCCCCTACAGAGATCAGAGTCCGGGGGCGGCAGCTG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:133238751..133238932 26863196 MeRIP-seq:(Medium) rs767952251 Functional Loss SNV dbSNP153 33..33 33 - - - 71652 RMVar_ID_71652 Human_SNP_ID_383230844 m1A Human chr8 + 133238835 133238835 133238835 GGGGGCGAAAAGGGGCCGGGGAGGAGGGGGCCACTACAGAGATCAGAGTCCGGGGGCGGCAGCTG GGGGGCGAAAAGGGGCCGGGGAGGAGGGGGCCGCTACAGAGATCAGAGTCCGGGGGCGGCAGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:133238751..133238932 26863196 MeRIP-seq:(Medium) rs767952251 Functional Loss SNV dbSNP153 33..33 33 - - - 71653 RMVar_ID_71653 Human_SNP_ID_383230904 m1A Human chr8 - 133238951 133238949 133238951 CCGCAGCCGCTCGCACACCAGCGAGGGGGCCCACCTGGACATCACCCCCAACTCGGGTGCTGCTG CCGCAGCCGCTCGCACACCAGCGAGGGGGCCCTTTTGGACATCACCCCCAACTCGGGTGCTGCTG GGT AAA NDRG1 Ensembl:ENSG00000104419 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133238901..133238975 32194978 MeRIP-seq:(Medium) rs1554747447 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_22465291 Human_miRNA_ID_2295360,Human_miRNA_ID_2873174,Human_miRNA_ID_2981137 Clinvar_Rec_298 RMVar_hsa_circ_89153,RMVar_hsa_circ_254544 71654 RMVar_ID_71654 Human_SNP_ID_383230906 m1A Human chr8 - 133238951 133238951 133238951 CCGCAGCCGCTCGCACACCAGCGAGGGGGCCCACCTGGACATCACCCCCAACTCGGGTGCTGCTG CCGCAGCCGCTCGCACACCAGCGAGGGGGCCCTCCTGGACATCACCCCCAACTCGGGTGCTGCTG T A NDRG1 Ensembl:ENSG00000104419 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133238901..133238975 32194978 MeRIP-seq:(Medium) rs759955688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22465291 Human_miRNA_ID_2295360,Human_miRNA_ID_2873174,Human_miRNA_ID_2981137 RMVar_hsa_circ_89153,RMVar_hsa_circ_254544 71655 RMVar_ID_71655 Human_SNP_ID_383230932 m1A Human chr8 - 133239009 133238980 133239010 GCAGCCGCTCCCACACCAGCGAGGGCACCCGAAGCCGCTCCCACACCAGCGAGGGCACCCGCAGC GCAGCCGCTCCCACACCAGCGAGGGCACCCG______________________________CAGC GCGGGTGCCCTCGCTGGTGTGGGAGCGGCTT G NDRG1 Ensembl:ENSG00000104419 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:133238958..133239063 26863196 MeRIP-seq:(Medium) rs751274009 Functional Loss DEL dbSNP153 32..61 33 - - - Human_RBP_ID_4995203,Human_RBP_ID_18472511 Human_miRNA_ID_2051396 RMVar_hsa_circ_89153,RMVar_hsa_circ_254544 71656 RMVar_ID_71656 Human_SNP_ID_383233500 m1A Human chr8 + 133248779 133248778 133248779 TCGCTCAATCTCCAGGTCGCGCCGGCTGCAGGAAACAAATGCATCATTAGCATGAGGACCCCTCC TCGCTCAATCTCCAGGTCGCGCCGGCTGCAGG_AACAAATGCATCATTAGCATGAGGACCCCTCC GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133248776..133248825 32194978 MeRIP-seq:(Medium) rs776996410 Functional Loss DEL dbSNP153 33..33 33 - - - 71657 RMVar_ID_71657 Human_SNP_ID_383243869 m1A Human chr8 - 133287989 133287987 133287989 TGAGAATGAAAGTTTGCAAGTGTGTCAGTGTGAGGGAATGTGTGAGTGCATTTGAGAGTGTGTGT TGAGAATGAAAGTTTGCAAGTGTGTCAGTGTG__GGAATGTGTGAGTGCATTTGAGAGTGTGTGT CCT C NDRG1 Ensembl:ENSG00000104419 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:133287984..133288137 26863196 MeRIP-seq:(Medium) rs1228486613 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5307758,Human_RBP_ID_24247161 RMVar_hsa_circ_85942,RMVar_hsa_circ_254548,RMVar_hsa_circ_62094 71658 RMVar_ID_71658 Human_SNP_ID_383245677 m1A Human chr8 + 133295319 133295319 133295319 GGCCAGGGGCCAGGTTACAGGGCAGGGCAGGCAAATCCTCCTCCTTGCCCAGATGCAGTGGGAGA GGCCAGGGGCCAGGTTACAGGGCAGGGCAGGCTAATCCTCCTCCTTGCCCAGATGCAGTGGGAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:133295315..133295476 26863196 MeRIP-seq:(Medium) rs1321001433 Functional Loss SNV dbSNP153 33..33 33 - - - 71659 RMVar_ID_71659 Human_SNP_ID_383246102 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAG________________________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 11..34 33 - - - 71660 RMVar_ID_71660 Human_SNP_ID_383246103 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGAC______________________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 13..34 33 - - - 71661 RMVar_ID_71661 Human_SNP_ID_383246104 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACAC____________________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 15..34 33 - - - 71662 RMVar_ID_71662 Human_SNP_ID_383246105 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACAC__________________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 17..34 33 - - - 71663 RMVar_ID_71663 Human_SNP_ID_383246106 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACAC________________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 19..34 33 - - - 71664 RMVar_ID_71664 Human_SNP_ID_383246107 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACAC______________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 21..34 33 - - - 71665 RMVar_ID_71665 Human_SNP_ID_383246108 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACAC____________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 23..34 33 - - - 71666 RMVar_ID_71666 Human_SNP_ID_383246109 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACAC__________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 25..34 33 - - - 71667 RMVar_ID_71667 Human_SNP_ID_383246110 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACACAC________ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 27..34 33 - - - 71668 RMVar_ID_71668 Human_SNP_ID_383246111 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACACACAC______ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 29..34 33 - - - 71669 RMVar_ID_71669 Human_SNP_ID_383246112 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACACACACAC____ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 31..34 33 - - - 71670 RMVar_ID_71670 Human_SNP_ID_383246113 m1A Human chr8 + 133296717 133296694 133296718 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACACACACACAC__ACACACACACACACTCACCTAGTCCCTTCTG GACACACACACACACACACACACAC GACACACACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs36215434 Functional Loss DEL dbSNP153 33..34 33 - - - 71671 RMVar_ID_71671 Human_SNP_ID_383246140 m1A Human chr8 + 133296717 133296717 133296717 CCAGACACAGACACACACACACACACACACACACACACACACACACACTCACCTAGTCCCTTCTG CCAGACACAGACACACACACACACACACACACTCACACACACACACACTCACCTAGTCCCTTCTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133296715..133296834 32194978 MeRIP-seq:(Medium) rs1353206091 Functional Loss SNV dbSNP153 33..33 33 - - - 71672 RMVar_ID_71672 Human_SNP_ID_383246263 m1A Human chr8 + 133297078 133297078 133297078 AAAGGGCGGTCCTGGCGCTCCAGCGGCACCGCACGGGCGGCCCCTTTCTGCTCCGCGTCGCGCCT AAAGGGCGGTCCTGGCGCTCCAGCGGCACCGCTCGGGCGGCCCCTTTCTGCTCCGCGTCGCGCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:133297073..133297168 26863196 MeRIP-seq:(Medium) rs902198346 Functional Loss SNV dbSNP153 33..33 33 - - - 71673 RMVar_ID_71673 Human_SNP_ID_383246307 m1A Human chr8 - 133297206 133297206 133297206 TCCCAGCTGGTGCTGAAGCTCGTCAGTTCACCATCCGCCCTCGGCTTCCGCGGGGCGCTGGGCCG TCCCAGCTGGTGCTGAAGCTCGTCAGTTCACCGTCCGCCCTCGGCTTCCGCGGGGCGCTGGGCCG T C NDRG1 Ensembl:ENSG00000104419 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:133297201..133297250 32194978 MeRIP-seq:(Medium) rs902469261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4971522,Human_RBP_ID_5514425,Human_RBP_ID_9338378,Human_RBP_ID_22465303 Human_Splice_Rec_1013733,Human_Splice_Rec_1013759,Human_Splice_Rec_1013819,Human_Splice_Rec_1013873,Human_Splice_Rec_1013883,Human_Splice_Rec_1013909,Human_Splice_Rec_1013945,Human_Splice_Rec_1013989,Human_Splice_Rec_1013999,Human_Splice_Rec_1014055,Human_Splice_Rec_1014083 Human_miRNA_ID_1956872,Human_miRNA_ID_3003869 RMVar_hsa_circ_85942,RMVar_hsa_circ_254548,RMVar_hsa_circ_62094 71674 RMVar_ID_71674 Human_SNP_ID_383299648 m1A Human chr8 - 133507951 133507951 133507951 TCCTCTGTGGCCAGAGGCAGTTCTCTGGATCAAGGGACAGCTGTGAGCTGTCAGCAGCCAATAGT TCCTCTGTGGCCAGAGGCAGTTCTCTGGATCAGGGGACAGCTGTGAGCTGTCAGCAGCCAATAGT T C ST3GAL1 Ensembl:ENSG00000008513 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:133507915..133508083 26863196 MeRIP-seq:(Medium) rs978212552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94238,RMVar_hsa_circ_254566,RMVar_hsa_circ_48025 71675 RMVar_ID_71675 Human_SNP_ID_383316664 m1A Human chr8 + 133572495 133572495 133572495 GGTGGGGAGAAGGGGCCGATCCCCTGCTGGCGACCGGGCAGAGCCACCCACTTCCTCTAAGGGCG GGTGGGGAGAAGGGGCCGATCCCCTGCTGGCGGCCGGGCAGAGCCACCCACTTCCTCTAAGGGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:133572285..133572505 26863196 MeRIP-seq:(Medium) rs1397987968 Functional Loss SNV dbSNP153 33..33 33 - - - 71676 RMVar_ID_71676 Human_SNP_ID_383556495 m1A Human chr8 - 134478693 134478691 134478694 GCAGGTCACCGAGGAGGAGCCCAGCTCCAACCACACGGTCATGATCCAGGAGACGGTCCAGCAAG GCAGGTCACCGAGGAGGAGCCCAGCTCCAAC___ACGGTCATGATCCAGGAGACGGTCCAGCAAG TGTG T ZFAT Ensembl:ENSG00000066827 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:134478587..134509685 32194978 MeRIP-seq:(Medium) rs1563753238 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1014258,Human_Splice_Rec_1014288,Human_Splice_Rec_1014320,Human_Splice_Rec_1014380,Human_Splice_Rec_1014412,Human_Splice_Rec_1014422,Human_Splice_Rec_1014452,Human_Splice_Rec_1014456,Human_Splice_Rec_1014484 71677 RMVar_ID_71677 Human_SNP_ID_383567833 m1A Human chr8 + 134522615 134522615 134522615 AAAACTTACAACTTTTATTGGCAAAGCCCTCCACGTCCTCAGCTACTTCTCTTTCTCTCAAACCT AAAACTTACAACTTTTATTGGCAAAGCCCTCCGCGTCCTCAGCTACTTCTCTTTCTCTCAAACCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:134522606..134522692 26863196 MeRIP-seq:(Medium) rs1403825552 Functional Loss SNV dbSNP153 33..33 33 - - - 71678 RMVar_ID_71678 Human_SNP_ID_383579543 m1A Human chr8 - 134570101 134570101 134570101 GCAGGTGCAGAGGCCCGGAGGTAGGTGCGTGGACTGTGTCTATGGAGTGGAGAGAGGTGAAGGCA GCAGGTGCAGAGGCCCGGAGGTAGGTGCGTGGGCTGTGTCTATGGAGTGGAGAGAGGTGAAGGCA T C ZFAT Ensembl:ENSG00000066827 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:134570085..134570159 26863196 MeRIP-seq:(Medium) rs1387718088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16367217 RMVar_hsa_circ_6336,RMVar_hsa_circ_299835,RMVar_hsa_circ_298009,RMVar_hsa_circ_115655,RMVar_hsa_circ_101771,RMVar_hsa_circ_59913,RMVar_hsa_circ_254573,RMVar_hsa_circ_254575,RMVar_hsa_circ_254574,RMVar_hsa_circ_254571,RMVar_hsa_circ_254572,RMVar_hsa_circ_254580,RMVar_hsa_circ_289907,RMVar_hsa_circ_298177,RMVar_hsa_circ_67112,RMVar_hsa_circ_254581,RMVar_hsa_circ_328443,RMVar_hsa_circ_287941,RMVar_hsa_circ_254583,RMVar_hsa_circ_254584 71679 RMVar_ID_71679 Human_SNP_ID_383584441 m1A Human chr8 + 134590574 134590499 134590575 CAACAGTCATCACCACCATCACTACTACCACCATCATCACCATCATCATCACCACCACCAGCACT __________________________________CATCACCATCATCATCACCACCACCAGCACT ACATCACCATCATCAATACCATCATCACCACCACTAGCACTATCAACAGTCATCACCACCATCACTACTACCACCAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:134590469..134590706 26863196 MeRIP-seq:(Medium) rs1563640851 Functional Loss DEL dbSNP153 1..34 33 - - - 71680 RMVar_ID_71680 Human_SNP_ID_383584470 m1A Human chr8 + 134590574 134590572 134590575 CAACAGTCATCACCACCATCACTACTACCACCATCATCACCATCATCATCACCACCACCAGCACT CAACAGTCATCACCACCATCACTACTACCAC___CATCACCATCATCATCACCACCACCAGCACT CCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:134590469..134590706 26863196 MeRIP-seq:(Medium) rs1168563758 Functional Loss DEL dbSNP153 32..34 33 - - - 71681 RMVar_ID_71681 Human_SNP_ID_341223899 m1A Human chr7 - 135166559 135166559 135166559 ACTGTCTGCCGAGAGCAGCTGGAGGACAGCTGAGCTTCCACTGGTGCTGCTGGGCCGCCCGCCTG ACTGTCTGCCGAGAGCAGCTGGAGGACAGCTGTGCTTCCACTGGTGCTGCTGGGCCGCCCGCCTG T A CYREN Ensembl:ENSG00000122783 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:135166448..135166689 26863196 MeRIP-seq:(Medium) rs949281895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675928,Human_RBP_ID_5479072,Human_RBP_ID_7700145,Human_RBP_ID_22111247,Human_RBP_ID_26551719,Human_RBP_ID_27352104 71682 RMVar_ID_71682 Human_SNP_ID_341223910 m1A Human chr7 - 135166596 135166596 135166596 GAGATCTTTTTCAGCTAGGGCATAAACTGTGCACTGAACTGTCTGCCGAGAGCAGCTGGAGGACA GAGATCTTTTTCAGCTAGGGCATAAACTGTGCGCTGAACTGTCTGCCGAGAGCAGCTGGAGGACA T C CYREN Ensembl:ENSG00000122783 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:135166546..135166669 26863196 MeRIP-seq:(Medium) rs767814896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675929,Human_RBP_ID_1682003,Human_RBP_ID_2035784,Human_RBP_ID_16024047,Human_RBP_ID_26551719,Human_RBP_ID_27528629 Human_miRNA_ID_329396,Human_miRNA_ID_333420,Human_miRNA_ID_350468 71683 RMVar_ID_71683 Human_SNP_ID_341225150 m1A Human chr7 + 135170349 135170349 135170349 GGCCCCGCGGGAACGCGATGTGCTGCCAGTTCACAGCCCGCCCTCCCTCTGCGGGCCGGTACCCG GGCCCCGCGGGAACGCGATGTGCTGCCAGTTCGCAGCCCGCCCTCCCTCTGCGGGCCGGTACCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:135170347..135170596 32194978 MeRIP-seq:(Medium) rs1394816166 Functional Loss SNV dbSNP153 33..33 33 - - - 71684 RMVar_ID_71684 Human_SNP_ID_341225274 m1A Human chr7 + 135170626 135170626 135170626 AGCTTCCAGAGCGGAGCCGGGAGGCAAATTCCAAGCGGTTGTGGGACCCACGCCTCACCCGGAAC AGCTTCCAGAGCGGAGCCGGGAGGCAAATTCCCAGCGGTTGTGGGACCCACGCCTCACCCGGAAC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:135170396..135170725 26863410 MeRIP-seq:(Medium) rs1230788822 Functional Loss SNV dbSNP153 33..33 33 - - - 71685 RMVar_ID_71685 Human_SNP_ID_341225289 m1A Human chr7 - 135170648 135170648 135170648 AGGCGAGACGGCAGGGCTTAAAGTTCCGGGTGAGGCGTGGGTCCCACAACCGCTTGGAATTTGCC AGGCGAGACGGCAGGGCTTAAAGTTCCGGGTGGGGCGTGGGTCCCACAACCGCTTGGAATTTGCC T C CYREN Ensembl:ENSG00000122783 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:135170533..135170665 26863196 MeRIP-seq:(Medium) rs1008676078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675933,Human_RBP_ID_4926208,Human_RBP_ID_18426433,Human_RBP_ID_19137435,Human_RBP_ID_22317572 71686 RMVar_ID_71686 Human_SNP_ID_341227062 m1A Human chr7 - 135176706 135176706 135176706 CACTGATCCCTCTCAAGCCTAGGCTGGCCTTCAAACCCTGGCCTAGCTTGTCCTCTACTGTGACC CACTGATCCCTCTCAAGCCTAGGCTGGCCTTCCAACCCTGGCCTAGCTTGTCCTCTACTGTGACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:135176656..135176784 26863196 MeRIP-seq:(Medium) rs1005570167 Functional Loss SNV dbSNP153 33..33 33 - - - 71687 RMVar_ID_71687 Human_SNP_ID_341235360 m1A Human chr7 - 135211462 135211462 135211462 GGCCGTGGAGCGCACTGACGAGCTGGTCCGGGAGTACCTGCTCTTCCGCGGGTTCACGCACACAC GGCCGTGGAGCGCACTGACGAGCTGGTCCGGGGGTACCTGCTCTTCCGCGGGTTCACGCACACAC T C WDR91 Ensembl:ENSG00000105875 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:135211380..135211500 26863196 MeRIP-seq:(Medium) rs778485286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_925933,Human_Splice_Rec_925959 RMVar_hsa_circ_121159,RMVar_hsa_circ_248689 71688 RMVar_ID_71688 Human_SNP_ID_341235375 m1A Human chr7 - 135211481 135211481 135211481 CTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCACTGACGAGCTGGTCCGGGAGTACCTGCTCTTC CTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCGCTGACGAGCTGGTCCGGGAGTACCTGCTCTTC T C WDR91 Ensembl:ENSG00000105875 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:135211325..135211525;chr7:135211307..135211505 26863196 MeRIP-seq:(Medium) rs759642179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4926231 RMVar_hsa_circ_121159,RMVar_hsa_circ_248689 71689 RMVar_ID_71689 Human_SNP_ID_341235376 m1A Human chr7 - 135211481 135211481 135211481 CTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCACTGACGAGCTGGTCCGGGAGTACCTGCTCTTC CTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCCCTGACGAGCTGGTCCGGGAGTACCTGCTCTTC T G WDR91 Ensembl:ENSG00000105875 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:135211325..135211525;chr7:135211307..135211505 26863196 MeRIP-seq:(Medium) rs759642179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4926231 RMVar_hsa_circ_121159,RMVar_hsa_circ_248689 71690 RMVar_ID_71690 Human_SNP_ID_341235384 m1A Human chr7 - 135211486 135211486 135211486 AGACGCTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCACTGACGAGCTGGTCCGGGAGTACCTGC AGACGCTAGCGCTGCGATGGCGGAGGCCGTGGTGCGCACTGACGAGCTGGTCCGGGAGTACCTGC T A WDR91 Ensembl:ENSG00000105875 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:135211375..135211517 26863196 MeRIP-seq:(Medium) rs752900701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121159,RMVar_hsa_circ_248689 71691 RMVar_ID_71691 Human_SNP_ID_341235385 m1A Human chr7 - 135211486 135211486 135211486 AGACGCTAGCGCTGCGATGGCGGAGGCCGTGGAGCGCACTGACGAGCTGGTCCGGGAGTACCTGC AGACGCTAGCGCTGCGATGGCGGAGGCCGTGGGGCGCACTGACGAGCTGGTCCGGGAGTACCTGC T C WDR91 Ensembl:ENSG00000105875 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:135211375..135211517 26863196 MeRIP-seq:(Medium) rs752900701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121159,RMVar_hsa_circ_248689 71692 RMVar_ID_71692 Human_SNP_ID_341271100 m1A Human chr7 - 135362923 135362923 135362923 AGACAGCCTTCAGACCCCCCAGCAAAACCCCCACAGATTTACTACAGAGTTCAACACTGGACCGC AGACAGCCTTCAGACCCCCCAGCAAAACCCCCCCAGATTTACTACAGAGTTCAACACTGGACCGC T G CNOT4 Ensembl:ENSG00000080802 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:135362874..135362982 26863196 MeRIP-seq:(Medium) rs1219674854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18960433 71693 RMVar_ID_71693 Human_SNP_ID_341302416 m1A Human chr7 - 135496578 135496578 135496578 TGTTGCTTCTAGGTAGCCAAGGAGGTTTCAGGAAGAAGGGCACAGAGGTGGACATAGTCCAATAC TGTTGCTTCTAGGTAGCCAAGGAGGTTTCAGGGAGAAGGGCACAGAGGTGGACATAGTCCAATAC T C CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:135496541..135496669 26863196 MeRIP-seq:(Medium) rs1026985103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9350933,Human_RBP_ID_16027342,Human_RBP_ID_23196942 71694 RMVar_ID_71694 Human_SNP_ID_341343989 m1A Human chr7 - 135662549 135662549 135662549 ATGATGTCGGTGGGGAGGGCGAGGAGGGCGCGAAGGACTGCAGCAGCTCCGCGGGCCGGTCCGAG ATGATGTCGGTGGGGAGGGCGAGGAGGGCGCGTAGGACTGCAGCAGCTCCGCGGGCCGGTCCGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:135662501..135662773 26863196 MeRIP-seq:(Medium) rs1176126860 Functional Loss SNV dbSNP153 33..33 33 - - - 71695 RMVar_ID_71695 Human_SNP_ID_341409150 m1A Human chr7 + 135928345 135928338 135928346 CACCTATACACCCACACACCCACATGCCAACCAACCAACCAACCAGCAACTGATCAGTAAAACTT CACCTATACACCCACACACCCACATG________CCAACCAACCAGCAACTGATCAGTAAAACTT GCCAACCAA G AC015987.1 Ensembl:ENSG00000224746 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:135928296..135928379 26863196 MeRIP-seq:(Medium) rs917729504 Functional Loss DEL dbSNP153 27..34 33 - - - 71696 RMVar_ID_71696 Human_SNP_ID_341409151 m1A Human chr7 + 135928345 135928338 135928346 CACCTATACACCCACACACCCACATGCCAACCAACCAACCAACCAGCAACTGATCAGTAAAACTT CACCTATACACCCACACACCCACATGCCAA____CCAACCAACCAGCAACTGATCAGTAAAACTT GCCAACCAA GCCAA AC015987.1 Ensembl:ENSG00000224746 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:135928296..135928379 26863196 MeRIP-seq:(Medium) rs917729504 Functional Loss DEL dbSNP153 31..34 33 - - - 71697 RMVar_ID_71697 Human_SNP_ID_341409154 m1A Human chr7 + 135928345 135928345 135928345 CACCTATACACCCACACACCCACATGCCAACCAACCAACCAACCAGCAACTGATCAGTAAAACTT CACCTATACACCCACACACCCACATGCCAACCTACCAACCAACCAGCAACTGATCAGTAAAACTT A T AC015987.1 Ensembl:ENSG00000224746 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:135928296..135928379 26863196 MeRIP-seq:(Medium) rs1408800638 Functional Loss SNV dbSNP153 33..33 33 - - - 71698 RMVar_ID_71698 Human_SNP_ID_341420474 m1A Human chr7 + 135977140 135977138 135977141 GCGGGGCAGGCCGGTTGGCCGGGCAGAAGATGAGGAGGCGGTGGCAGCAGCAAGCGGATGCCGCC GCGGGGCAGGCCGGTTGGCCGGGCAGAAGAT___GAGGCGGTGGCAGCAGCAAGCGGATGCCGCC TGAG T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:135977026..135977350 26863196 MeRIP-seq:(Medium) rs773805314 Functional Loss DEL dbSNP153 32..34 33 - - - 71699 RMVar_ID_71699 Human_SNP_ID_341420483 m1A Human chr7 - 135977149 135977149 135977149 CTCTCGCCCGGCGGCATCCGCTTGCTGCTGCCACCGCCTCCTCATCTTCTGCCCGGCCAACCGGC CTCTCGCCCGGCGGCATCCGCTTGCTGCTGCCTCCGCCTCCTCATCTTCTGCCCGGCCAACCGGC T A MTPN Ensembl:ENSG00000105887 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:135977101..135977350 26863196 MeRIP-seq:(Medium) rs1390032644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1050673,Human_RBP_ID_4960359,Human_RBP_ID_5429118,Human_RBP_ID_5451887,Human_RBP_ID_17427166,Human_RBP_ID_18876744,Human_RBP_ID_22463782,Human_RBP_ID_24193939,Human_RBP_ID_27528744 RMVar_hsa_circ_119289,RMVar_hsa_circ_248782 71700 RMVar_ID_71700 Human_SNP_ID_341420495 m1A Human chr7 + 135977180 135977180 135977180 GTGGCAGCAGCAAGCGGATGCCGCCGGGCGAGAGGGAGGCAGGGCCGCGCGAAGCCGGAGAGGAG GTGGCAGCAGCAAGCGGATGCCGCCGGGCGAGCGGGAGGCAGGGCCGCGCGAAGCCGGAGAGGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:135977131..135977321 26863196 MeRIP-seq:(Medium) rs1001325984 Functional Loss SNV dbSNP153 33..33 33 - - - 71701 RMVar_ID_71701 Human_SNP_ID_341420523 m1A Human chr7 + 135977248 135977248 135977248 AAGAGAAGGAGGGTTAGGCTGCCAGGCGGGCGAGGCAGTTGGCCGCGGCGACCGTTCGGGCGGGA AAGAGAAGGAGGGTTAGGCTGCCAGGCGGGCGGGGCAGTTGGCCGCGGCGACCGTTCGGGCGGGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr7:135977177..135977302;chr7:135977076..135977375 26863410 MeRIP-seq:(Medium) rs1279141836 Functional Loss SNV dbSNP153 33..33 33 - - - 71702 RMVar_ID_71702 Human_SNP_ID_341755556 m1A Human chr7 - 137343541 137343541 137343541 CGTCCAGAAGGCGGGGAGAGCAGCAGCGGCCCAAGCAGGAGCTGCAGCGAGCCGGGTACCTGGAC CGTCCAGAAGGCGGGGAGAGCAGCAGCGGCCCGAGCAGGAGCTGCAGCGAGCCGGGTACCTGGAC T C PTN Ensembl:ENSG00000105894 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:137343490..137343592 26863196 MeRIP-seq:(Medium) rs375486448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176562 71703 RMVar_ID_71703 Human_SNP_ID_341755574 m1A Human chr7 - 137343568 137343568 137343568 GGGGAAGAAAGAGACCAGTGAGTCATCCGTCCAGAAGGCGGGGAGAGCAGCAGCGGCCCAAGCAG GGGGAAGAAAGAGACCAGTGAGTCATCCGTCCGGAAGGCGGGGAGAGCAGCAGCGGCCCAAGCAG T C PTN Ensembl:ENSG00000105894 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:137343522..137343669 26863196 MeRIP-seq:(Medium) rs1443475760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176562 71704 RMVar_ID_71704 Human_SNP_ID_341882341 m1A Human chr7 + 137878298 137878298 137878298 AAAACCCAGTCTGGTTCAGTTGCAGCAGGTACATGGGTTGGCTCATTCTCTCACTTCTGCCCCTA AAAACCCAGTCTGGTTCAGTTGCAGCAGGTACGTGGGTTGGCTCATTCTCTCACTTCTGCCCCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:137878247..137878425 26863196 MeRIP-seq:(Medium) rs761084361 Functional Loss SNV dbSNP153 33..33 33 - - - 71705 RMVar_ID_71705 Human_SNP_ID_341882812 m1A Human chr7 - 137879974 137879974 137879974 GTGTGAACACCCCCGACAGCAGCCCTCCGCCCACTCTGCCCCCTGGGAGCCCTCGCTGGATCGTC GTGTGAACACCCCCGACAGCAGCCCTCCGCCCGCTCTGCCCCCTGGGAGCCCTCGCTGGATCGTC T C CREB3L2 Ensembl:ENSG00000182158 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:137879926..137880055 26863196 MeRIP-seq:(Medium) rs1224476060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253779,Human_RBP_ID_17316225,Human_RBP_ID_17427173,Human_RBP_ID_17543279,Human_RBP_ID_24515161 RMVar_hsa_circ_248852,RMVar_hsa_circ_85848,RMVar_hsa_circ_122351,RMVar_hsa_circ_248853 71706 RMVar_ID_71706 Human_SNP_ID_341890042 m1A Human chr7 - 137908309 137908309 137908309 TTCAGCCTGCCTCAGACCCACAGCCCCTCCAGAGCTGCACCCCGGGCCCCCTCCGCCCTCTCCAG TTCAGCCTGCCTCAGACCCACAGCCCCTCCAGTGCTGCACCCCGGGCCCCCTCCGCCCTCTCCAG T A CREB3L2 Ensembl:ENSG00000182158 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:137908251..137908425 26863196 MeRIP-seq:(Medium) rs761706677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18960451 Human_Splice_Rec_927199,Human_Splice_Rec_927221,Human_Splice_Rec_927249 Human_miRNA_ID_2012385,Human_miRNA_ID_2758759,Human_miRNA_ID_2792460 RMVar_hsa_circ_26117,RMVar_hsa_circ_85848,RMVar_hsa_circ_248853,RMVar_hsa_circ_100568,RMVar_hsa_circ_328832,RMVar_hsa_circ_248857,RMVar_hsa_circ_84368,RMVar_hsa_circ_248856,RMVar_hsa_circ_248858,RMVar_hsa_circ_117994,RMVar_hsa_circ_355957,RMVar_hsa_circ_270526,RMVar_hsa_circ_14930,RMVar_hsa_circ_25220,RMVar_hsa_circ_248859,RMVar_hsa_circ_290722,RMVar_hsa_circ_297156 71707 RMVar_ID_71707 Human_SNP_ID_341890057 m1A Human chr7 - 137908376 137908376 137908376 CACCCCTCCGAGCAGTCACGGCAGTGACTCAGAGGGCAGCCTGAGTCCCAACCCACGCCTGCACC CACCCCTCCGAGCAGTCACGGCAGTGACTCAGGGGGCAGCCTGAGTCCCAACCCACGCCTGCACC T C CREB3L2 Ensembl:ENSG00000182158 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:137908326..137908400 26863196 MeRIP-seq:(Medium) rs961979124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17543471 Human_Splice_Rec_927198,Human_Splice_Rec_927220,Human_Splice_Rec_927248 Human_miRNA_ID_2770388 RMVar_hsa_circ_26117,RMVar_hsa_circ_85848,RMVar_hsa_circ_248853,RMVar_hsa_circ_100568,RMVar_hsa_circ_328832,RMVar_hsa_circ_248857,RMVar_hsa_circ_84368,RMVar_hsa_circ_248856,RMVar_hsa_circ_248858,RMVar_hsa_circ_117994,RMVar_hsa_circ_355957,RMVar_hsa_circ_270526,RMVar_hsa_circ_14930,RMVar_hsa_circ_25220,RMVar_hsa_circ_248859,RMVar_hsa_circ_290722,RMVar_hsa_circ_297156 71708 RMVar_ID_71708 Human_SNP_ID_341890525 m1A Human chr7 - 137910219 137910219 137910219 CGCAATGAGAGAGAGAAGAAAAAAAGCATGCCAGGGCCGGGGGGACCAGGGTTGGCTGACGGGGC CGCAATGAGAGAGAGAAGAAAAAAAGCATGCCTGGGCCGGGGGGACCAGGGTTGGCTGACGGGGC T A CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:137910217..137910321 26863196 MeRIP-seq:(Medium) rs184108530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26117,RMVar_hsa_circ_100568,RMVar_hsa_circ_248857,RMVar_hsa_circ_84368,RMVar_hsa_circ_248856,RMVar_hsa_circ_248858,RMVar_hsa_circ_117994,RMVar_hsa_circ_270526,RMVar_hsa_circ_14930,RMVar_hsa_circ_25220,RMVar_hsa_circ_248859,RMVar_hsa_circ_297156 71709 RMVar_ID_71709 Human_SNP_ID_341903040 m1A Human chr7 - 137961780 137961780 137961780 AGAAGCAGCAAAGGATGAATGGAAGAATTGCCAAGGGCAGAGCTTAGAGCGGAGTGACCAAGGTG AGAAGCAGCAAAGGATGAATGGAAGAATTGCCGAGGGCAGAGCTTAGAGCGGAGTGACCAAGGTG T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:137961764..137962032 26863196 MeRIP-seq:(Medium) rs573669225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16032687,Human_RBP_ID_24194218 71710 RMVar_ID_71710 Human_SNP_ID_341903046 m1A Human chr7 - 137961802 137961802 137961802 GGGGTAGGCTAGAGATCTTTCAAGAAGCAGCAAAGGATGAATGGAAGAATTGCCAAGGGCAGAGC GGGGTAGGCTAGAGATCTTTCAAGAAGCAGCAGAGGATGAATGGAAGAATTGCCAAGGGCAGAGC T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:137961783..137962004 26863196 MeRIP-seq:(Medium) rs1273729828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16032687,Human_RBP_ID_24194218 71711 RMVar_ID_71711 Human_SNP_ID_341903048 m1A Human chr7 - 137961820 137961820 137961820 ATCATGGAGGAAAGGCCTGGGGTAGGCTAGAGATCTTTCAAGAAGCAGCAAAGGATGAATGGAAG ATCATGGAGGAAAGGCCTGGGGTAGGCTAGAGGTCTTTCAAGAAGCAGCAAAGGATGAATGGAAG T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:137961801..137961887 26863196 MeRIP-seq:(Medium) rs1214470128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23297447 71712 RMVar_ID_71712 Human_SNP_ID_341912909 m1A Human chr7 - 138001500 138001500 138001500 GTCCTGGGACCCGGGAAGGCAGGGTTTGGGGCAGGGCATGGTCAGAATCAAGAGGTCCTGGGCGA GTCCTGGGACCCGGGAAGGCAGGGTTTGGGGCGGGGCATGGTCAGAATCAAGAGGTCCTGGGCGA T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:138001453..138001607 26863196 MeRIP-seq:(Medium) rs1357286279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3063033,Human_RBP_ID_24389166 71713 RMVar_ID_71713 Human_SNP_ID_341912910 m1A Human chr7 - 138001500 138001500 138001500 GTCCTGGGACCCGGGAAGGCAGGGTTTGGGGCAGGGCATGGTCAGAATCAAGAGGTCCTGGGCGA GTCCTGGGACCCGGGAAGGCAGGGTTTGGGGCCGGGCATGGTCAGAATCAAGAGGTCCTGGGCGA T G CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:138001453..138001607 26863196 MeRIP-seq:(Medium) rs1357286279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3063033,Human_RBP_ID_24389166 71714 RMVar_ID_71714 Human_SNP_ID_342132719 m1A Human chr7 + 138837992 138837992 138837992 CTCGCGGATTGCTTTGATGAGAGAGGCCGAGGAGTGGCCAGGCTGGAGGTCTTCCGTGGAGCTGG CTCGCGGATTGCTTTGATGAGAGAGGCCGAGGGGTGGCCAGGCTGGAGGTCTTCCGTGGAGCTGG A G TMEM213 Ensembl:ENSG00000214128 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:138837951..138838051 32194978 MeRIP-seq:(Medium) rs774024519 Functional Loss SNV dbSNP153 33..33 33 - - - 71715 RMVar_ID_71715 Human_SNP_ID_342135077 m1A Human chr7 + 138847050 138847050 138847050 GCTCCTCCTTCAAGAACTGTAAACCGGAGCCCACACCTCACCTAATCACAGTCTCTGGACCATCC GCTCCTCCTTCAAGAACTGTAAACCGGAGCCCGCACCTCACCTAATCACAGTCTCTGGACCATCC A G HSALNG0061686 RNACentral:URS0000E932C7 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:138847046..138847129 26863196 MeRIP-seq:(Medium) rs1019360388 Functional Loss SNV dbSNP153 33..33 33 - - - 71716 RMVar_ID_71716 Human_SNP_ID_342166377 m1A Human chr7 - 138971389 138971389 138971389 ATCTAGGGCAAGAGTGGAGGCATTCATTTGAGAGAGGAGGAAAACAGAAGGAGAAACAGGTGGCT ATCTAGGGCAAGAGTGGAGGCATTCATTTGAGGGAGGAGGAAAACAGAAGGAGAAACAGGTGGCT T C KIAA1549 Ensembl:ENSG00000122778 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:138971374..138971529 26863196 MeRIP-seq:(Medium) rs1040976723 Functional Loss SNV dbSNP153 33..33 33 - - - 71717 RMVar_ID_71717 Human_SNP_ID_342168729 m1A Human chr7 - 138981243 138981243 138981243 CCGGGAATGCCGGGGGCGCGGCGCCGACGCCGAGGCGCGGCCATGGAGGGGAAGCCCCGCGCCGG CCGGGAATGCCGGGGGCGCGGCGCCGACGCCGGGGCGCGGCCATGGAGGGGAAGCCCCGCGCCGG T C KIAA1549 Ensembl:ENSG00000122778 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:138981145..138981331 26863410 MeRIP-seq:(Medium) rs1173095083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794267,Human_RBP_ID_4956001 71718 RMVar_ID_71718 Human_SNP_ID_342168756 m1A Human chr7 - 138981317 138981317 138981317 CCAGCCGCAGCCGCAGCGGCCGCCCCTCCCGGACCCGAGAGCCGCTGAGCCGCGAGGCCGGGCCG CCAGCCGCAGCCGCAGCGGCCGCCCCTCCCGGGCCCGAGAGCCGCTGAGCCGCGAGGCCGGGCCG T C KIAA1549 Ensembl:ENSG00000122778 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:138981267..138981340 26863196 MeRIP-seq:(Medium) rs1184832799 Functional Loss SNV dbSNP153 33..33 33 - - - 71719 RMVar_ID_71719 Human_SNP_ID_342185134 m1A Human chr7 - 139045279 139045279 139045279 CACTCTGGCTTCCTTTCAGTTTTGTGGTTCCCATTTTTAGCTAGTTCAGTGGTTTTCAATGGGCA CACTCTGGCTTCCTTTCAGTTTTGTGGTTCCCGTTTTTAGCTAGTTCAGTGGTTTTCAATGGGCA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17314974,Human_RBP_ID_24439227 GWAS_ID_8738,GWAS_ID_8739,GWAS_ID_8740,GWAS_ID_8741,GWAS_ID_8742,GWAS_ID_8743,GWAS_ID_8744,GWAS_ID_8745,GWAS_ID_8746,GWAS_ID_8747,GWAS_ID_8748,GWAS_ID_8749,GWAS_ID_8750,GWAS_ID_8751,GWAS_ID_8752 RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 71720 RMVar_ID_71720 Human_SNP_ID_342185199 m1A Human chr7 - 139045615 139045615 139045615 CCTCTCTCAGGATCTGTATGTAAGTGAAAAGCATCACCATCTACCCATTGGCTCAAGCAGAAATC CCTCTCTCAGGATCTGTATGTAAGTGAAAAGCGTCACCATCTACCCATTGGCTCAAGCAGAAATC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7803490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1113848,Human_RBP_ID_17314976 GWAS_ID_8753,GWAS_ID_8754,GWAS_ID_8755,GWAS_ID_8756 RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 71721 RMVar_ID_71721 Human_SNP_ID_342191251 m1A Human chr7 - 139069593 139069593 139069593 TGATGATTGAATCGATGGGCAGTTGGGCAGCAATGGTGTAGGGTAGAGTGATAGCAGGGCTGACA TGATGATTGAATCGATGGGCAGTTGGGCAGCAGTGGTGTAGGGTAGAGTGATAGCAGGGCTGACA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139069566..139069649 26863196 MeRIP-seq:(Medium) rs368352310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26284,RMVar_hsa_circ_80839,RMVar_hsa_circ_78777,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_341540,RMVar_hsa_circ_359082,RMVar_hsa_circ_248940,RMVar_hsa_circ_248941,RMVar_hsa_circ_55993,RMVar_hsa_circ_311764,RMVar_hsa_circ_352336 71722 RMVar_ID_71722 Human_SNP_ID_342191259 m1A Human chr7 - 139069615 139069615 139069615 GAGGGTGTGGTATTAGGAGAAGTGATGATTGAATCGATGGGCAGTTGGGCAGCAATGGTGTAGGG GAGGGTGTGGTATTAGGAGAAGTGATGATTGACTCGATGGGCAGTTGGGCAGCAATGGTGTAGGG T G ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:139069564..139069649 26863196 MeRIP-seq:(Medium) rs957354521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24194768 RMVar_hsa_circ_26284,RMVar_hsa_circ_80839,RMVar_hsa_circ_78777,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_341540,RMVar_hsa_circ_359082,RMVar_hsa_circ_248940,RMVar_hsa_circ_248941,RMVar_hsa_circ_55993,RMVar_hsa_circ_311764,RMVar_hsa_circ_352336 71723 RMVar_ID_71723 Human_SNP_ID_342197216 m1A Human chr7 - 139092783 139092783 139092783 AATAAGAAGTTTGCCTGAGGATGGAGATGAAAAATGAGAAGGAAAACCAGGCCCCCAGGTGGGCA AATAAGAAGTTTGCCTGAGGATGGAGATGAAAGATGAGAAGGAAAACCAGGCCCCCAGGTGGGCA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:139092777..139092917 26863196 MeRIP-seq:(Medium) rs924030372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 71724 RMVar_ID_71724 Human_SNP_ID_342197221 m1A Human chr7 - 139092798 139092797 139092798 CACAGAATCTAGAGGAATAAGAAGTTTGCCTGAGGATGGAGATGAAAAATGAGAAGGAAAACCAG CACAGAATCTAGAGGAATAAGAAGTTTGCCTG_GGATGGAGATGAAAAATGAGAAGGAAAACCAG CT C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139092776..139092942 26863196 MeRIP-seq:(Medium) rs1253565580 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 71725 RMVar_ID_71725 Human_SNP_ID_342207965 m1A Human chr7 - 139133827 139133827 139133827 ATCTTGACGTCGGTCTTGTGAGTCCCCACCACACAGCGAAGGCCGCGCCTCAGCGTTTCGCCGCA ATCTTGACGTCGGTCTTGTGAGTCCCCACCACTCAGCGAAGGCCGCGCCTCAGCGTTTCGCCGCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139133777..139134788 26863196 MeRIP-seq:(Medium) rs774036859 Functional Loss SNV dbSNP153 33..33 33 - - - 71726 RMVar_ID_71726 Human_SNP_ID_342230960 m1A Human chr7 + 139231309 139231309 139231309 GCGACCCTGGCGATGGCGGTGAAGCCCATCAGAACGTAGTAGCGGGGAAGGGGACACGGTCCGCA GCGACCCTGGCGATGGCGGTGAAGCCCATCAGGACGTAGTAGCGGGGAAGGGGACACGGTCCGCA A G UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:139231265..139231397;chr7:139231259..139231940;chr7:139231259..139231582 26863196 MeRIP-seq:(Medium) rs1264491580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952833,Human_RBP_ID_3972625,Human_RBP_ID_26357167 71727 RMVar_ID_71727 Human_SNP_ID_342230962 m1A Human chr7 + 139231317 139231317 139231317 GGCGATGGCGGTGAAGCCCATCAGAACGTAGTAGCGGGGAAGGGGACACGGTCCGCACTCACCGT GGCGATGGCGGTGAAGCCCATCAGAACGTAGTGGCGGGGAAGGGGACACGGTCCGCACTCACCGT A G UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:139231267..139231619 26863196 MeRIP-seq:(Medium) rs1487714704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952833,Human_RBP_ID_3972625,Human_RBP_ID_4927241,Human_RBP_ID_26357167 71728 RMVar_ID_71728 Human_SNP_ID_342231240 m1A Human chr7 + 139231888 139231888 139231888 GGAGACGGTGCGCCTGGAGCTGGTGCTTAAGGACCCCACCGACGAGAGCTGCGTGGAGTTCAGTT GGAGACGGTGCGCCTGGAGCTGGTGCTTAAGGGCCCCACCGACGAGAGCTGCGTGGAGTTCAGTT A G UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:139231841..139231941 32194978 MeRIP-seq:(Medium) rs1160194312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23080174 Human_Splice_Rec_928287 71729 RMVar_ID_71729 Human_SNP_ID_342246125 m1A Human chr7 - 139288418 139288418 139288418 CAGGCTCTTTTCCATCTCAGTGTCTTCATACAACTGTTCCCTCTGGCCTGAACTATTTTCCCCCT CAGGCTCTTTTCCATCTCAGTGTCTTCATACAGCTGTTCCCTCTGGCCTGAACTATTTTCCCCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139288375..139288472 26863196 MeRIP-seq:(Medium) rs1418617010 Functional Loss SNV dbSNP153 33..33 33 - - - 71730 RMVar_ID_71730 Human_SNP_ID_342259818 m1A Human chr7 + 139341371 139341368 139341371 GGTCGTAGGACGCCGTTGGGCACCACGCTCGGAGAAGGACAGGACAATGGCGGCCTTAGGGTCCC GGTCGTAGGACGCCGTTGGGCACCACGCTC___GAAGGACAGGACAATGGCGGCCTTAGGGTCCC CGGA C FMC1-LUC7L2,FMC1,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000164898,Ensembl:ENSG00000146963 Protein coding,Protein coding,Protein coding 5'UTR,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1183986087 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_676862,Human_RBP_ID_4927353,Human_RBP_ID_16038137 71731 RMVar_ID_71731 Human_SNP_ID_342265041 m1A Human chr7 + 139360075 139360075 139360075 GTCGCTGTCGGGGGCTGTCGTCTTCCACGTACACGTCGTCGTGAGGAGCGCAGTCCGGACTCTTC GTCGCTGTCGGGGGCTGTCGTCTTCCACGTACGCGTCGTCGTGAGGAGCGCAGTCCGGACTCTTC A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:139359978..139360300 26863196 MeRIP-seq:(Medium) rs929537977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87349,Human_RBP_ID_676880,Human_RBP_ID_1050738,Human_RBP_ID_1682413,Human_RBP_ID_2036286,Human_RBP_ID_4927391,Human_RBP_ID_5134917,Human_RBP_ID_5429147,Human_RBP_ID_5451922,Human_RBP_ID_5479118,Human_RBP_ID_5512692,Human_RBP_ID_7703820,Human_RBP_ID_8659788,Human_RBP_ID_8908599,Human_RBP_ID_16038288,Human_RBP_ID_18876921,Human_RBP_ID_23080713,Human_RBP_ID_26077778,Human_RBP_ID_27528926 RMVar_hsa_circ_34626 71732 RMVar_ID_71732 Human_SNP_ID_342265099 m1A Human chr7 + 139360209 139360209 139360209 TCCCCCATCCCTTCCCCTTATCCCCCAGCCCAAAAGGGCCCGGTCTGCGCCCCACCCCCGCCCGT TCCCCCATCCCTTCCCCTTATCCCCCAGCCCAGAAGGGCCCGGTCTGCGCCCCACCCCCGCCCGT A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:139359849..139360325 26863196 MeRIP-seq:(Medium) rs965152862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254377,Human_RBP_ID_676882,Human_RBP_ID_4960488,Human_RBP_ID_5134607,Human_RBP_ID_5429155,Human_RBP_ID_5451930,Human_RBP_ID_5479127,Human_RBP_ID_5512699,Human_RBP_ID_9337404,Human_RBP_ID_17092731,Human_RBP_ID_18876924,Human_RBP_ID_18959675,Human_RBP_ID_22317999,Human_RBP_ID_22833501,Human_RBP_ID_27106073 Human_Splice_Rec_928372 RMVar_hsa_circ_34626 71733 RMVar_ID_71733 Human_SNP_ID_342265169 m1A Human chr7 - 139360313 139360313 139360313 CCAGGGCCCTGGCAGAGACTTACCGTCCCGGGAGGTGCCCATCAACTGGTCCAGCATCGCGCGCA CCAGGGCCCTGGCAGAGACTTACCGTCCCGGGTGGTGCCCATCAACTGGTCCAGCATCGCGCGCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:139360216..139360317 32194978 MeRIP-seq:(Medium) rs955699458 Functional Loss SNV dbSNP153 33..33 33 - - - 71734 RMVar_ID_71734 Human_SNP_ID_342282403 m1A Human chr7 + 139423010 139423010 139423010 AATCAAACGTCTTGATTTTTCTGTTCTGTTGAATTGCTATGTTCAGGATGTTCTAGGGGGTGGGG AATCAAACGTCTTGATTTTTCTGTTCTGTTGATTTGCTATGTTCAGGATGTTCTAGGGGGTGGGG A T LUC7L2 Ensembl:ENSG00000146963 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:139422959..139423059 32194978 MeRIP-seq:(Medium) rs1484483581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677031,Human_RBP_ID_1682550,Human_RBP_ID_2036494,Human_RBP_ID_3064132,Human_RBP_ID_3834925,Human_RBP_ID_5122916,Human_RBP_ID_5153765,Human_RBP_ID_7704706,Human_RBP_ID_8951896,Human_RBP_ID_9205803,Human_RBP_ID_16041185,Human_RBP_ID_17665472,Human_RBP_ID_18172258,Human_RBP_ID_18379324,Human_RBP_ID_24195482,Human_RBP_ID_24439239,Human_RBP_ID_24515301,Human_RBP_ID_26722466 Human_miRNA_ID_2586793,Human_miRNA_ID_2698736 RMVar_hsa_circ_102933,RMVar_hsa_circ_249012 71735 RMVar_ID_71735 Human_SNP_ID_342321181 m1A Human chr7 - 139568034 139568034 139568034 AGCTTGGGGTGGAAGATTTAGGCCGTGTGAGCATGTGTGAGTGAGTGGAACAAACTTTCTTGGAA AGCTTGGGGTGGAAGATTTAGGCCGTGTGAGCGTGTGTGAGTGAGTGGAACAAACTTTCTTGGAA T C HIPK2 Ensembl:ENSG00000064393 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1638195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5220299,Human_RBP_ID_8659989,Human_RBP_ID_24195617 Human_miRNA_ID_2539468 GWAS_ID_8757 RMVar_hsa_circ_98038,RMVar_hsa_circ_267067,RMVar_hsa_circ_376739,RMVar_hsa_circ_249015,RMVar_hsa_circ_249016 71736 RMVar_ID_71736 Human_SNP_ID_342322415 m1A Human chr7 - 139572620 139572620 139572620 ATCTATGGTTTTTATTTTAAAAAAGAAAAAGGAAAAAAAAAAAGTCAATAACAAAAAACCCAGCT ATCTATGGTTTTTATTTTAAAAAAGAAAAAGGGAAAAAAAAAAGTCAATAACAAAAAACCCAGCT T C HIPK2 Ensembl:ENSG00000064393 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:139572583..139572721 26863196 MeRIP-seq:(Medium) rs1569439978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677267,Human_RBP_ID_8238309,Human_RBP_ID_26544469 RMVar_hsa_circ_98038,RMVar_hsa_circ_267067,RMVar_hsa_circ_376739,RMVar_hsa_circ_249015,RMVar_hsa_circ_249016 71737 RMVar_ID_71737 Human_SNP_ID_342344161 m1A Human chr7 + 139663103 139663103 139663103 GTCCATGACCTTCGACACTAATTCCTGCTCACACTTCCCTCAGCCCAGGAACTCTCCCTGCATCC GTCCATGACCTTCGACACTAATTCCTGCTCACGCTTCCCTCAGCCCAGGAACTCTCCCTGCATCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139663057..139663206 26863196 MeRIP-seq:(Medium) rs770053414 Functional Loss SNV dbSNP153 33..33 33 - - - 71738 RMVar_ID_71738 Human_SNP_ID_342354172 m1A Human chr7 - 139704167 139704167 139704167 GGGTGTGTATGTTGGATATAGTGTGGGTGTGGAGGGGGTGTATGTGTTGGGTATGGTGTGTGTGT GGGTGTGTATGTTGGATATAGTGTGGGTGTGGGGGGGGTGTATGTGTTGGGTATGGTGTGTGTGT T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:139704120..139704247 26863196 MeRIP-seq:(Medium) rs1484420390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5657254,Human_RBP_ID_9351278,Human_RBP_ID_21992579,Human_RBP_ID_22483903 RMVar_hsa_circ_56255 71739 RMVar_ID_71739 Human_SNP_ID_342354184 m1A Human chr7 + 139704201 139704200 139704202 CACACCCACACTATATCCAACATACACACCCAACACACACACCACACCCAACACACACTACACCC CACACCCACACTATATCCAACATACACACCCA__ACACACACCACACCCAACACACACTACACCC AAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:139704071..139704527 26863196 MeRIP-seq:(Medium) rs1169915220 Functional Loss DEL dbSNP153 33..34 33 - - - 71740 RMVar_ID_71740 Human_SNP_ID_342357357 m1A Human chr7 - 139716812 139716812 139716812 CCACAACCGTCAGCACCTCCTTGCCGGTCCCAAACCCAAGCCTACCTTACGAGCAGACCATCGTC CCACAACCGTCAGCACCTCCTTGCCGGTCCCATACCCAAGCCTACCTTACGAGCAGACCATCGTC T A HIPK2 Ensembl:ENSG00000064393 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139716761..139716940 26863196 MeRIP-seq:(Medium) rs769698027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17315476,Human_RBP_ID_17427183,Human_RBP_ID_17543297,Human_RBP_ID_27106288 RMVar_hsa_circ_56255,RMVar_hsa_circ_92512,RMVar_hsa_circ_287234,RMVar_hsa_circ_249026,RMVar_hsa_circ_249027 71741 RMVar_ID_71741 Human_SNP_ID_342371742 m1A Human chr7 + 139777746 139777744 139777746 TTGAGCCTGTGTCTCCGCTCTCGGCGCAGCCGAGGCCGCCCGCGCCCGCATCACCGCCTCCCGTG TTGAGCCTGTGTCTCCGCTCTCGGCGCAGCC__GGCCGCCCGCGCCCGCATCACCGCCTCCCGTG CGA C TBXAS1 Ensembl:ENSG00000059377 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:139777616..139777776 26863196 MeRIP-seq:(Medium) rs1218973168 Functional Loss DEL dbSNP153 32..33 33 - - - 71742 RMVar_ID_71742 Human_SNP_ID_342371835 m1A Human chr7 + 139777943 139777943 139777943 CGAGCGGCCGCGGCCCCCGAGCGGATCCGCGGAGGGGCGGGAGCCGGGGGCAGCGCGCGGCCAGG CGAGCGGCCGCGGCCCCCGAGCGGATCCGCGGGGGGGCGGGAGCCGGGGGCAGCGCGCGGCCAGG A G TBXAS1 Ensembl:ENSG00000059377 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr7:139777736..139778025;chr7:139777851..139778025 26863410 MeRIP-seq:(Medium) rs1269479911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18466656 71743 RMVar_ID_71743 Human_SNP_ID_342371836 m1A Human chr7 + 139777943 139777943 139777943 CGAGCGGCCGCGGCCCCCGAGCGGATCCGCGGAGGGGCGGGAGCCGGGGGCAGCGCGCGGCCAGG CGAGCGGCCGCGGCCCCCGAGCGGATCCGCGGTGGGGCGGGAGCCGGGGGCAGCGCGCGGCCAGG A T TBXAS1 Ensembl:ENSG00000059377 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr7:139777736..139778025;chr7:139777851..139778025 26863410 MeRIP-seq:(Medium) rs1269479911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18466656 71744 RMVar_ID_71744 Human_SNP_ID_342372398 m1A Human chr7 + 139779925 139779925 139779925 GTGCCTTTGCCCAAGCGGTCACTTTCCCACCCACTTTCCCAGAGGGGTACCTTCTCCATCTTCTC GTGCCTTTGCCCAAGCGGTCACTTTCCCACCCTCTTTCCCAGAGGGGTACCTTCTCCATCTTCTC A T TBXAS1 Ensembl:ENSG00000059377 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:139779800..139780102 26863410 MeRIP-seq:(Medium) rs948708269 Functional Loss SNV dbSNP153 33..33 33 - - - 71745 RMVar_ID_71745 Human_SNP_ID_342471183 m1A Human chr7 + 140177275 140177275 140177275 GCGGGGGCGGAGGGAGCTGAGGCCCCGTGAGGACACGCGCGGTGGTGGCGGTGGCGGCGGGCGCG GCGGGGGCGGAGGGAGCTGAGGCCCCGTGAGGCCACGCGCGGTGGTGGCGGTGGCGGCGGGCGCG A C KDM7A-DT Ensembl:ENSG00000260231 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:140177226..140177608;chr7:140177231..140177608 26863196 MeRIP-seq:(Medium) rs1260427205 Functional Loss SNV dbSNP153 33..33 33 - - - 71746 RMVar_ID_71746 Human_SNP_ID_342523617 m1A Human chr7 + 140390367 140390367 140390367 CTAGAAACCTAGTTACATGGTTAGCAGGCACTATATCCTCACAAGACTCCGGGTGCTCCCTATAC CTAGAAACCTAGTTACATGGTTAGCAGGCACTTTATCCTCACAAGACTCCGGGTGCTCCCTATAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:140390363..140390510 26863196 MeRIP-seq:(Medium) rs886802200 Functional Loss SNV dbSNP153 33..33 33 - - - 71747 RMVar_ID_71747 Human_SNP_ID_342523672 m1A Human chr7 - 140390584 140390584 140390584 GGGAGTGCGAGGGAGATCAGTCCCTGACATCTATGGGGAACAGCAGGCTATAGAGCCCCAAGGTG GGGAGTGCGAGGGAGATCAGTCCCTGACATCTGTGGGGAACAGCAGGCTATAGAGCCCCAAGGTG T C SLC37A3 Ensembl:ENSG00000157800 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:140390575..140390720 26863196 MeRIP-seq:(Medium) rs1385182292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269083 71748 RMVar_ID_71748 Human_SNP_ID_342525565 m1A Human chr7 - 140398466 140398466 140398466 CGGCGGGGGAGGCGGGCAGCGGAGCCAAGCTGACCCGGCGAGCGGAGCCGGGGCTGGAGAGCGGC CGGCGGGGGAGGCGGGCAGCGGAGCCAAGCTGCCCCGGCGAGCGGAGCCGGGGCTGGAGAGCGGC T G SLC37A3 Ensembl:ENSG00000157800 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:140398335..140398493;chr7:140398373..140398490 26863196 MeRIP-seq:(Medium) rs1452643213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254398,Human_RBP_ID_794384,Human_RBP_ID_955014,Human_RBP_ID_3971489,Human_RBP_ID_4956011,Human_RBP_ID_18426109,Human_RBP_ID_19021537,Human_RBP_ID_23080182,Human_RBP_ID_24563126 Human_Splice_Rec_929117,Human_Splice_Rec_929147,Human_Splice_Rec_929169,Human_Splice_Rec_929195,Human_Splice_Rec_929255,Human_Splice_Rec_929311,Human_Splice_Rec_929321,Human_Splice_Rec_929355,Human_Splice_Rec_929365,Human_Splice_Rec_929373,Human_Splice_Rec_929383 RMVar_hsa_circ_269083 71749 RMVar_ID_71749 Human_SNP_ID_342541046 m1A Human chr7 + 140454650 140454650 140454650 TAAGCAACATCTCGCCCAGCTCAAAGGTGACAACCTCTTCTTCATCGTTGTCAAAGGGGTTGCTG TAAGCAACATCTCGCCCAGCTCAAAGGTGACAGCCTCTTCTTCATCGTTGTCAAAGGGGTTGCTG A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:140454601..140454752 26863196 MeRIP-seq:(Medium) rs1062786 Functional Loss SNV dbSNP153 33..33 33 - - - 71750 RMVar_ID_71750 Human_SNP_ID_342541197 m1A Human chr7 - 140455123 140455123 140455123 CCCTGATGGCCGTAGAGAGGAGCCACAGAGACAGAAAGTGGGAACATCAAGCAGATACCGGGTAA CCCTGATGGCCGTAGAGAGGAGCCACAGAGACGGAAAGTGGGAACATCAAGCAGATACCGGGTAA T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:140455095..140455245 32194978 MeRIP-seq:(Medium) rs1183504347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26357207 Human_Splice_Rec_929421,Human_Splice_Rec_929433,Human_Splice_Rec_929443,Human_Splice_Rec_929457,Human_Splice_Rec_929461,Human_Splice_Rec_929467 RMVar_hsa_circ_41297,RMVar_hsa_circ_51329,RMVar_hsa_circ_368804 71751 RMVar_ID_71751 Human_SNP_ID_342542273 m1A Human chr7 - 140459151 140459151 140459151 GAATCAGAGAAAGAGCAAACCGCCGTGGAGACAAAGAAGCAGCTGTGCCCCTATGCTGCAGTGGG GAATCAGAGAAAGAGCAAACCGCCGTGGAGACGAAGAAGCAGCTGTGCCCCTATGCTGCAGTGGG T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:140459101..140459714 32194978 MeRIP-seq:(Medium) rs1245381626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956233,Human_RBP_ID_9205915,Human_RBP_ID_16279996,Human_RBP_ID_18877243 Human_Splice_Rec_929414,Human_Splice_Rec_929428,Human_Splice_Rec_929450,Human_Splice_Rec_929482,Human_Splice_Rec_929490,Human_Splice_Rec_929498,Human_Splice_Rec_929506,Human_Splice_Rec_929512 RMVar_hsa_circ_123123,RMVar_hsa_circ_41297,RMVar_hsa_circ_51329,RMVar_hsa_circ_99268,RMVar_hsa_circ_249087,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662,RMVar_hsa_circ_249088,RMVar_hsa_circ_325699 71752 RMVar_ID_71752 Human_SNP_ID_342542274 m1A Human chr7 - 140459153 140459153 140459153 AAGAATCAGAGAAAGAGCAAACCGCCGTGGAGACAAAGAAGCAGCTGTGCCCCTATGCTGCAGTG AAGAATCAGAGAAAGAGCAAACCGCCGTGGAGGCAAAGAAGCAGCTGTGCCCCTATGCTGCAGTG T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:140459103..140459172 26863196 MeRIP-seq:(Medium) rs750041308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956233,Human_RBP_ID_9205915,Human_RBP_ID_16279996,Human_RBP_ID_18877243 Human_Splice_Rec_929414,Human_Splice_Rec_929428,Human_Splice_Rec_929450,Human_Splice_Rec_929482,Human_Splice_Rec_929490,Human_Splice_Rec_929498,Human_Splice_Rec_929506,Human_Splice_Rec_929512 RMVar_hsa_circ_123123,RMVar_hsa_circ_41297,RMVar_hsa_circ_51329,RMVar_hsa_circ_99268,RMVar_hsa_circ_249087,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662,RMVar_hsa_circ_249088,RMVar_hsa_circ_325699 71753 RMVar_ID_71753 Human_SNP_ID_342546273 m1A Human chr7 - 140471984 140471984 140471984 CACAGGTATTTTATGCATGGGGTTTGTAAGGAAGGAGACAACTGTCGCTACTCGCATGACCTCTC CACAGGTATTTTATGCATGGGGTTTGTAAGGAGGGAGACAACTGTCGCTACTCGCATGACCTCTC T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:140471936..140472055 26863196 MeRIP-seq:(Medium) rs142729794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677472,Human_RBP_ID_1682700,Human_RBP_ID_7706024,Human_RBP_ID_16045131,Human_RBP_ID_17312055,Human_RBP_ID_18108236,Human_RBP_ID_18877251,Human_RBP_ID_22686015,Human_RBP_ID_24196231 Human_Splice_Rec_929410,Human_Splice_Rec_929424,Human_Splice_Rec_929436,Human_Splice_Rec_929446,Human_Splice_Rec_929470,Human_Splice_Rec_929478,Human_Splice_Rec_929486,Human_Splice_Rec_929494,Human_Splice_Rec_929502,Human_Splice_Rec_929508,Human_Splice_Rec_929524,Human_Splice_Rec_929532,Human_Splice_Rec_929536 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662,RMVar_hsa_circ_295560 71754 RMVar_ID_71754 Human_SNP_ID_342546280 m1A Human chr7 - 140472000 140472000 140472000 TTGTGGTCTTTCGTCTCACAGGTATTTTATGCATGGGGTTTGTAAGGAAGGAGACAACTGTCGCT TTGTGGTCTTTCGTCTCACAGGTATTTTATGCGTGGGGTTTGTAAGGAAGGAGACAACTGTCGCT T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:140471926..140472226 26863196 MeRIP-seq:(Medium) rs572012392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677472,Human_RBP_ID_1682700,Human_RBP_ID_4960624,Human_RBP_ID_7706024,Human_RBP_ID_16045133,Human_RBP_ID_18108236,Human_RBP_ID_18877251,Human_RBP_ID_22686015,Human_RBP_ID_24196231 Human_Splice_Rec_929410,Human_Splice_Rec_929424,Human_Splice_Rec_929436,Human_Splice_Rec_929446,Human_Splice_Rec_929470,Human_Splice_Rec_929478,Human_Splice_Rec_929486,Human_Splice_Rec_929494,Human_Splice_Rec_929502,Human_Splice_Rec_929508,Human_Splice_Rec_929524,Human_Splice_Rec_929532,Human_Splice_Rec_929536 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662,RMVar_hsa_circ_295560 71755 RMVar_ID_71755 Human_SNP_ID_342548940 m1A Human chr7 - 140479124 140479124 140479124 GGACGTTGCGCGGCGGAGCGCCGGGCGCGGGGAGGGGGCCGCGGGCCAAGCCTGCGGCGCGGGAG GGACGTTGCGCGGCGGAGCGCCGGGCGCGGGGGGGGGGCCGCGGGCCAAGCCTGCGGCGCGGGAG T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:140479123..140479275 26863410 MeRIP-seq:(Medium) rs933591233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19135523 71756 RMVar_ID_71756 Human_SNP_ID_342549010 m1A Human chr7 - 140479260 140479260 140479260 CGGCAGCGGCGACGGCGGCAGCAGCCTCCCCCACCCCGATCCCCACAGTCACCGCCCCGTCCCTG CGGCAGCGGCGACGGCGGCAGCAGCCTCCCCCCCCCCGATCCCCACAGTCACCGCCCCGTCCCTG T G MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:140479127..140479270 26863410 MeRIP-seq:(Medium) rs889148960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4960626,Human_RBP_ID_5451951,Human_RBP_ID_5512722,Human_RBP_ID_17427190 71757 RMVar_ID_71757 Human_SNP_ID_342549057 m1A Human chr7 - 140479308 140479305 140479308 CGGAGGCTGCAACTCCCGGAACAACAGCCACAACATCAGGAGCAGGAGCGGCAGCGGCGACGGCG CGGAGGCTGCAACTCCCGGAACAACAGCCACA___TCAGGAGCAGGAGCGGCAGCGGCGACGGCG ATGT A MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:140479119..140479488 26863196 MeRIP-seq:(Medium) rs749334129 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4956717 71758 RMVar_ID_71758 Human_SNP_ID_342549059 m1A Human chr7 - 140479309 140479309 140479309 GCGGAGGCTGCAACTCCCGGAACAACAGCCACAACATCAGGAGCAGGAGCGGCAGCGGCGACGGC GCGGAGGCTGCAACTCCCGGAACAACAGCCACGACATCAGGAGCAGGAGCGGCAGCGGCGACGGC T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:140479109..140479464 26863196 MeRIP-seq:(Medium) rs1457135327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956717,Human_RBP_ID_26831818 71759 RMVar_ID_71759 Human_SNP_ID_342549061 m1A Human chr7 - 140479311 140479311 140479311 TGGCGGAGGCTGCAACTCCCGGAACAACAGCCACAACATCAGGAGCAGGAGCGGCAGCGGCGACG TGGCGGAGGCTGCAACTCCCGGAACAACAGCCGCAACATCAGGAGCAGGAGCGGCAGCGGCGACG T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:140479151..140479375;chr7:140479118..140479487 26863196 MeRIP-seq:(Medium) rs1430580572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956717,Human_RBP_ID_16045173,Human_RBP_ID_26831818 71760 RMVar_ID_71760 Human_SNP_ID_342590971 m1A Human chr7 - 140640685 140640685 140640685 GCGGGGACCCCACGGGAGCGCGCGCGGCGGGGACCCCCAGGGGCTTGCGGGCGGCCGGGGGAGGC GCGGGGACCCCACGGGAGCGCGCGCGGCGGGGGCCCCCAGGGGCTTGCGGGCGGCCGGGGGAGGC T C DENND2A Ensembl:ENSG00000146966 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:140640591..140640798 26863196 MeRIP-seq:(Medium) rs1027545835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84102,RMVar_hsa_circ_249102 71761 RMVar_ID_71761 Human_SNP_ID_342599077 m1A Human chr7 - 140672996 140672996 140672996 GGGGGCCGCGCGGGCGGAGGCAGGGGCCGGGCAGCCGCAGGGTCACCGTGCGCCCAGGGGCCAGT GGGGGCCGCGCGGGCGGAGGCAGGGGCCGGGCCGCCGCAGGGTCACCGTGCGCCCAGGGGCCAGT T G DENND2A Ensembl:ENSG00000146966 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:140672952..140673267 26863196 MeRIP-seq:(Medium) rs1214069910 Functional Loss SNV dbSNP153 33..33 33 - - - 71762 RMVar_ID_71762 Human_SNP_ID_342599113 m1A Human chr7 + 140673108 140673108 140673108 CTCCTCCCGTTCCGCAGTTGGTGCCGTCTGACAGCCCCTTCCGCGCGGCGCGGCGCGGCGCGGCG CTCCTCCCGTTCCGCAGTTGGTGCCGTCTGACGGCCCCTTCCGCGCGGCGCGGCGCGGCGCGGCG A G ADCK2 Ensembl:ENSG00000133597 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:140672986..140673112 26863196 MeRIP-seq:(Medium) rs553887467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677487,Human_RBP_ID_5479150 Clinvar_Rec_299 71763 RMVar_ID_71763 Human_SNP_ID_342599406 m1A Human chr7 + 140673725 140673725 140673725 CCTGGCTCCCAGCGTCTCCACCCTCTGGCTCCACCTGCTTCTGAAAGCCACCGAGACCTCAGGCC CCTGGCTCCCAGCGTCTCCACCCTCTGGCTCCGCCTGCTTCTGAAAGCCACCGAGACCTCAGGCC A G ADCK2 Ensembl:ENSG00000133597 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:140673676..140673850 32194978 MeRIP-seq:(Medium) rs1389412434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_677491,Human_RBP_ID_4960649,Human_RBP_ID_27352803 RMVar_hsa_circ_87081,RMVar_hsa_circ_249110 71764 RMVar_ID_71764 Human_SNP_ID_342602644 m1A Human chr7 - 140687219 140687219 140687219 TGCGTCTCACCTGCCCCATCACCACAGCCATGAAAACTGCCCGGAAATTCCTCAGGTCAGGGGCC TGCGTCTCACCTGCCCCATCACCACAGCCATGGAAACTGCCCGGAAATTCCTCAGGTCAGGGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:140687170..140687275 26863196 MeRIP-seq:(Medium) rs1273315811 Functional Loss SNV dbSNP153 33..33 33 - - - 71765 RMVar_ID_71765 Human_SNP_ID_342605058 m1A Human chr7 - 140696744 140696744 140696744 GCGAAAGACGCCAGCCGAGTCAGAGCGGACATACTCGCTCCCGTCCGCCCCGCGGTCCCCAGCCG GCGAAAGACGCCAGCCGAGTCAGAGCGGACATGCTCGCTCCCGTCCGCCCCGCGGTCCCCAGCCG T C NDUFB2-AS1 Ensembl:ENSG00000240889 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr7:140696701..140696862;chr7:140696723..140696811 26863196,26863410 MeRIP-seq:(Medium) rs1412368891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929886 71766 RMVar_ID_71766 Human_SNP_ID_342605060 m1A Human chr7 - 140696748 140696748 140696748 GCGAGCGAAAGACGCCAGCCGAGTCAGAGCGGACATACTCGCTCCCGTCCGCCCCGCGGTCCCCA GCGAGCGAAAGACGCCAGCCGAGTCAGAGCGGCCATACTCGCTCCCGTCCGCCCCGCGGTCCCCA T G NDUFB2-AS1 Ensembl:ENSG00000240889 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:140696699..140696850 26863196 MeRIP-seq:(Medium) rs751941055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929886 71767 RMVar_ID_71767 Human_SNP_ID_342605197 m1A Human chr7 + 140697072 140697072 140697072 TGGGCAGATGGGACACCGTGTGCAGGGCCGTCATGGTAGTAGGGGCCGCCTGCCCTCGGGAGACG TGGGCAGATGGGACACCGTGTGCAGGGCCGTCGTGGTAGTAGGGGCCGCCTGCCCTCGGGAGACG A G NDUFB2 Ensembl:ENSG00000090266 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:140697069..140697220 26863196 MeRIP-seq:(Medium) rs924572625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860785,Human_RBP_ID_8218557,Human_RBP_ID_18504221 Human_Splice_Rec_929845,Human_Splice_Rec_929851 RMVar_hsa_circ_116814,RMVar_hsa_circ_249116,RMVar_hsa_circ_103384,RMVar_hsa_circ_249115 71768 RMVar_ID_71768 Human_SNP_ID_342661373 m1A Human chr7 + 140924653 140924653 140924653 CCGGCCTCGGGCTCCATGTCCCCGTTGAACAGAGCCTGGCCCGGCTCCGCGCCGCCACCACCGCC CCGGCCTCGGGCTCCATGTCCCCGTTGAACAGGGCCTGGCCCGGCTCCGCGCCGCCACCACCGCC A G RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:140924570..140924902 26863196 MeRIP-seq:(Medium) rs1037987633 Functional Loss SNV dbSNP153 33..33 33 - - - 71769 RMVar_ID_71769 Human_SNP_ID_342661449 m1A Human chr7 + 140924783 140924783 140924783 GGGGAAGGGAGGCGGAGAGCTGGGGGAGGCGGAGGCGGAGGCGGAGGCGGAGGAGCGGGGGGCGC GGGGAAGGGAGGCGGAGAGCTGGGGGAGGCGGGGGCGGAGGCGGAGGCGGAGGAGCGGGGGGCGC A G RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:140924777..140924909 26863196 MeRIP-seq:(Medium) rs1362861708 Functional Loss SNV dbSNP153 33..33 33 - - - 71770 RMVar_ID_71770 Human_SNP_ID_342682865 m1A Human chr7 - 141014860 141014860 141014860 TTGGGGGTCTGCAGCAAGGGGCGATGGCTGCGAAGTCTACGGGGGTCTCCAACCTTGTAGAGTCG TTGGGGGTCTGCAGCAAGGGGCGATGGCTGCGCAGTCTACGGGGGTCTCCAACCTTGTAGAGTCG T G MRPS33 Ensembl:ENSG00000090263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:141014859..141014926 26863196 MeRIP-seq:(Medium) rs1563069672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254127 71771 RMVar_ID_71771 Human_SNP_ID_342805882 m1A Human chr7 + 141551453 141551453 141551453 CTGGACCAGCCGTGGTGAGTGCAGCGGCGCCCAGGCGGGGAGCGCAGTGCGGGTCGCTGGGACTG CTGGACCAGCCGTGGTGAGTGCAGCGGCGCCCGGGCGGGGAGCGCAGTGCGGGTCGCTGGGACTG A G AGK Ensembl:ENSG00000006530 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:141551441..141551702 26863196 MeRIP-seq:(Medium) rs1053852870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842979,Human_RBP_ID_19135525 Human_Splice_Rec_930729,Human_Splice_Rec_930757 71772 RMVar_ID_71772 Human_SNP_ID_342805910 m1A Human chr7 - 141551484 141551484 141551484 CCCATCCCGACTCCCACCCCGCTCGCGCGCTCAGTCCCAGCGACCCGCACTGCGCTCCCCGCCTG CCCATCCCGACTCCCACCCCGCTCGCGCGCTCCGTCCCAGCGACCCGCACTGCGCTCCCCGCCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:141551433..141551617 26863196 MeRIP-seq:(Medium) rs1487657309 Functional Loss SNV dbSNP153 33..33 33 - - - 71773 RMVar_ID_71773 Human_SNP_ID_342805953 m1A Human chr7 + 141551598 141551598 141551598 GCGGGGACCCAAGCATCAGGGGTCGTGGGTGCAGGCGGCGGCGCGGCTTGAGGGTAGGGGGTGCG GCGGGGACCCAAGCATCAGGGGTCGTGGGTGCGGGCGGCGGCGCGGCTTGAGGGTAGGGGGTGCG A G AGK Ensembl:ENSG00000006530 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:141551517..141551630 26863196 MeRIP-seq:(Medium) rs1032264151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337419 Human_Splice_Rec_930787 71774 RMVar_ID_71774 Human_SNP_ID_342813019 m1A Human chr7 - 141583283 141583283 141583283 CCTCCTTCACTATAGGCAACTTTCCACCCTCCATTCCTCCTTCTTCTCCCTTAGCCTGTGTTCTC CCTCCTTCACTATAGGCAACTTTCCACCCTCCGTTCCTCCTTCTTCTCCCTTAGCCTGTGTTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:141583281..141583380 26863196 MeRIP-seq:(Medium) rs1198475305 Functional Loss SNV dbSNP153 33..33 33 - - - 71775 RMVar_ID_71775 Human_SNP_ID_342827840 m1A Human chr7 - 141652993 141652993 141652993 GGGACCCTCTGACGACACTGTTGGGATGGCTGAGGCACCTGTTCCCTTTTGGTCCCACCGGTGGC GGGACCCTCTGACGACACTGTTGGGATGGCTGGGGCACCTGTTCCCTTTTGGTCCCACCGGTGGC T C AC004918.1 Ensembl:ENSG00000244701 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:141652944..141653045 32194978 MeRIP-seq:(Medium) rs1301055159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5626074 71776 RMVar_ID_71776 Human_SNP_ID_342848588 m1A Human chr7 + 141738451 141738451 141738451 GGAAGGGATAGCCAGCGCGAAGGAAGTGCTGGAGTCGTGTGTTTTGGCTGCGCGTGATCCTGCGT GGAAGGGATAGCCAGCGCGAAGGAAGTGCTGGCGTCGTGTGTTTTGGCTGCGCGTGATCCTGCGT A C SSBP1 Ensembl:ENSG00000106028 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:141738376..141738525 26863410 MeRIP-seq:(Medium) rs937890033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4957891,Human_RBP_ID_9337421,Human_RBP_ID_18426444,Human_RBP_ID_22833614,Human_RBP_ID_23215682,Human_RBP_ID_24197324 Human_Splice_Rec_931125,Human_Splice_Rec_931199 RMVar_hsa_circ_86085,RMVar_hsa_circ_249210 71777 RMVar_ID_71777 Human_SNP_ID_342849958 m1A Human chr7 - 141743553 141743553 141743553 CCAAGTAAGTGCACACGATTCAGGGCTGAAACACAACATCAAGACCAAATGAGACAACCTGCTAT CCAAGTAAGTGCACACGATTCAGGGCTGAAACTCAACATCAAGACCAAATGAGACAACCTGCTAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:141743551..141743600 26863196 MeRIP-seq:(Medium) rs1355525477 Functional Loss SNV dbSNP153 33..33 33 - - - 71778 RMVar_ID_71778 Human_SNP_ID_343095905 m1A Human chr7 + 142667227 142667227 142667227 CATAATCACTTGTTCCTTAAATAGGGACTTGTATGAATGACCCCACGAGGGTTCAGCTGTCTCTT CATAATCACTTGTTCCTTAAATAGGGACTTGTGTGAATGACCCCACGAGGGTTCAGCTGTCTCTT A G MTRNR2L6 Ensembl:ENSG00000270672 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:142667005..142667314 26863196 MeRIP-seq:(Medium) rs1398799945 Functional Loss SNV dbSNP153 33..33 33 - - - 71779 RMVar_ID_71779 Human_SNP_ID_343095913 m1A Human chr7 + 142667239 142667239 142667239 TTCCTTAAATAGGGACTTGTATGAATGACCCCACGAGGGTTCAGCTGTCTCTTACTTCCAACCAG TTCCTTAAATAGGGACTTGTATGAATGACCCCTCGAGGGTTCAGCTGTCTCTTACTTCCAACCAG A T MTRNR2L6 Ensembl:ENSG00000270672 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:142667026..142667355 26863196 MeRIP-seq:(Medium) rs1310209559 Functional Loss SNV dbSNP153 33..33 33 - - - 71780 RMVar_ID_71780 Human_SNP_ID_343177597 m1A Human chr7 + 142962399 142962399 142962399 CTCTGGGTGGAGCCTGCTTATCAGTGGGGGGCACCCAGGCTTCTCCTCCCCCTTTATCTCAGCTT CTCTGGGTGGAGCCTGCTTATCAGTGGGGGGCGCCCAGGCTTCTCCTCCCCCTTTATCTCAGCTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:142962395..142962482 26863410 MeRIP-seq:(Medium) rs573735587 Functional Loss SNV dbSNP153 33..33 33 - - - 71781 RMVar_ID_71781 Human_SNP_ID_343248662 m1A Human chr7 - 143263536 143263536 143263536 AGTAGGGGGACAGCACGTCATAGAAGAGCTCCACGGTGCGCGGCAGGGGCCCCATGCTGCAGGCT AGTAGGGGGACAGCACGTCATAGAAGAGCTCCCCGGTGCGCGGCAGGGGCCCCATGCTGCAGGCT T G AC073342.1 Ensembl:ENSG00000231840 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:143263487..143263663 26863196 MeRIP-seq:(Medium) rs760271864 Functional Loss SNV dbSNP153 33..33 33 - - - 71782 RMVar_ID_71782 Human_SNP_ID_343249025 m1A Human chr7 + 143264720 143264719 143264721 GGGATGTAGACAGGGTATCCAGTGAAAAACACAGAAGTCGGAGATTGAGGGATTGATAGGATGGA GGGATGTAGACAGGGTATCCAGTGAAAAACAC__AAGTCGGAGATTGAGGGATTGATAGGATGGA CAG C GSTK1 Ensembl:ENSG00000197448 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:143264712..143264959 26863196 MeRIP-seq:(Medium) rs778972785 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_87569,Human_RBP_ID_24197637 RMVar_hsa_circ_2577,RMVar_hsa_circ_279170,RMVar_hsa_circ_342061 71783 RMVar_ID_71783 Human_SNP_ID_343249026 m1A Human chr7 + 143264720 143264720 143264720 GGGATGTAGACAGGGTATCCAGTGAAAAACACAGAAGTCGGAGATTGAGGGATTGATAGGATGGA GGGATGTAGACAGGGTATCCAGTGAAAAACACGGAAGTCGGAGATTGAGGGATTGATAGGATGGA A G GSTK1 Ensembl:ENSG00000197448 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:143264712..143264959 26863196 MeRIP-seq:(Medium) rs755757877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87569,Human_RBP_ID_24197637 RMVar_hsa_circ_2577,RMVar_hsa_circ_279170,RMVar_hsa_circ_342061 71784 RMVar_ID_71784 Human_SNP_ID_343250051 m1A Human chr7 - 143268809 143268809 143268809 AATCTTAAAGTCTGGCATTCACGGCTGGAGGTATAGGGCCCATCCACTTCTCTCCTGGATGAAGA AATCTTAAAGTCTGGCATTCACGGCTGGAGGTGTAGGGCCCATCCACTTCTCTCCTGGATGAAGA T C AC073342.1 Ensembl:ENSG00000231840 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:143268801..143268850 32194978 MeRIP-seq:(Medium) rs141399902 Functional Loss SNV dbSNP153 33..33 33 - - - 71785 RMVar_ID_71785 Human_SNP_ID_343253625 m1A Human chr7 - 143285006 143285006 143285006 GGTCCCAATCCCATGACCCTCCCGACCCTCGCACCCACACCTGTCTCAGAAGTTCGTCGCTCACC GGTCCCAATCCCATGACCCTCCCGACCCTCGCCCCCACACCTGTCTCAGAAGTTCGTCGCTCACC T G AC073342.1 Ensembl:ENSG00000231840 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143284982..143285109 26863196 MeRIP-seq:(Medium) rs1243996346 Functional Loss SNV dbSNP153 33..33 33 - - - 71786 RMVar_ID_71786 Human_SNP_ID_343255425 m1A Human chr7 + 143291484 143291484 143291484 TTTGTTCTTCCTATTCATGCCTCTTCCACTCCACTCTTCTGTGTCAAATTGTGACTTGACAGCCT TTTGTTCTTCCTATTCATGCCTCTTCCACTCCGCTCTTCTGTGTCAAATTGTGACTTGACAGCCT A G CASP2 Ensembl:ENSG00000106144 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:143291483..143291650 26863196 MeRIP-seq:(Medium) rs4647287 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_3065636,Human_RBP_ID_7708801,Human_RBP_ID_17637291,Human_RBP_ID_21560160 71787 RMVar_ID_71787 Human_SNP_ID_343278301 m1A Human chr7 + 143380526 143380526 143380526 GCCCGCGTCCGCGTCCGTCCTCCCGGGTCTCCAGTCCGCAGGCGGCCGCCGCCTCGGCCCCGCCC GCCCGCGTCCGCGTCCGTCCTCCCGGGTCTCCGGTCCGCAGGCGGCCGCCGCCTCGGCCCCGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143380475..143380578 26863196 MeRIP-seq:(Medium) rs1238935983 Functional Loss SNV dbSNP153 33..33 33 - - - 71788 RMVar_ID_71788 Human_SNP_ID_343278302 m1A Human chr7 + 143380526 143380526 143380526 GCCCGCGTCCGCGTCCGTCCTCCCGGGTCTCCAGTCCGCAGGCGGCCGCCGCCTCGGCCCCGCCC GCCCGCGTCCGCGTCCGTCCTCCCGGGTCTCCTGTCCGCAGGCGGCCGCCGCCTCGGCCCCGCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143380475..143380578 26863196 MeRIP-seq:(Medium) rs1238935983 Functional Loss SNV dbSNP153 33..33 33 - - - 71789 RMVar_ID_71789 Human_SNP_ID_343278621 m1A Human chr7 + 143381377 143381377 143381377 GCAGAGTCTGCGGACCCGGCGCCGAGGCGGCCACCCGAGACGCGGCGCGCACGCTCCGGCCTGCG GCAGAGTCTGCGGACCCGGCGCCGAGGCGGCCTCCCGAGACGCGGCGCGCACGCTCCGGCCTGCG A T ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:143381326..143381710 26863196 MeRIP-seq:(Medium) rs1438239350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956019 Human_Splice_Rec_933083,Human_Splice_Rec_933089,Human_Splice_Rec_933107 71790 RMVar_ID_71790 Human_SNP_ID_343278774 m1A Human chr7 + 143381668 143381668 143381668 CGCAGAAGAAGTTCGGCCCTGTGGTGGCCCCAAAGCCCAAAGTGAATCCCTTCCGGCCCGGGGAC CGCAGAAGAAGTTCGGCCCTGTGGTGGCCCCAGAGCCCAAAGTGAATCCCTTCCGGCCCGGGGAC A G ZYX Ensembl:ENSG00000159840 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:143381301..143381837 26863196 MeRIP-seq:(Medium) rs910264793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956737,Human_RBP_ID_9337424 RMVar_hsa_circ_2163,RMVar_hsa_circ_9427 71791 RMVar_ID_71791 Human_SNP_ID_343279059 m1A Human chr7 + 143382348 143382348 143382348 TTCCCGCCGCCCCCTCCCCCGATCGAGGAATCATTTCCCCCTGCGCCTCTGGAGGAGGAGATCTT TTCCCGCCGCCCCCTCCCCCGATCGAGGAATCGTTTCCCCCTGCGCCTCTGGAGGAGGAGATCTT A G ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:143382226..143382450 26863196 MeRIP-seq:(Medium) rs1203740730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678096,Human_RBP_ID_4929219,Human_RBP_ID_22534354 Human_Splice_Rec_933085,Human_Splice_Rec_933093,Human_Splice_Rec_933115,Human_Splice_Rec_933119,Human_Splice_Rec_933133 RMVar_hsa_circ_2163,RMVar_hsa_circ_9427,RMVar_hsa_circ_44615 71792 RMVar_ID_71792 Human_SNP_ID_343279060 m1A Human chr7 + 143382348 143382348 143382348 TTCCCGCCGCCCCCTCCCCCGATCGAGGAATCATTTCCCCCTGCGCCTCTGGAGGAGGAGATCTT TTCCCGCCGCCCCCTCCCCCGATCGAGGAATCTTTTCCCCCTGCGCCTCTGGAGGAGGAGATCTT A T ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:143382226..143382450 26863196 MeRIP-seq:(Medium) rs1203740730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678096,Human_RBP_ID_4929219,Human_RBP_ID_22534354 Human_Splice_Rec_933085,Human_Splice_Rec_933093,Human_Splice_Rec_933115,Human_Splice_Rec_933119,Human_Splice_Rec_933133 RMVar_hsa_circ_2163,RMVar_hsa_circ_9427,RMVar_hsa_circ_44615 71793 RMVar_ID_71793 Human_SNP_ID_343279350 m1A Human chr7 + 143382967 143382967 143382967 TCCGGCTCCGGCTCAGAGCCAGACACAGTTCCATGTTCAGCCCCAGCCCCAGCCCAAGCCTCAGG TCCGGCTCCGGCTCAGAGCCAGACACAGTTCCGTGTTCAGCCCCAGCCCCAGCCCAAGCCTCAGG A G ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:143382801..143383259 26863196 MeRIP-seq:(Medium) rs11978404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87395,Human_RBP_ID_794693,Human_RBP_ID_4929231,Human_RBP_ID_5134608,Human_RBP_ID_17092740,Human_RBP_ID_17315004,Human_RBP_ID_17427199,Human_RBP_ID_18959692,Human_RBP_ID_21396052,Human_RBP_ID_27106738 Human_miRNA_ID_1360781 71794 RMVar_ID_71794 Human_SNP_ID_343279351 m1A Human chr7 + 143382967 143382967 143382967 TCCGGCTCCGGCTCAGAGCCAGACACAGTTCCATGTTCAGCCCCAGCCCCAGCCCAAGCCTCAGG TCCGGCTCCGGCTCAGAGCCAGACACAGTTCCTTGTTCAGCCCCAGCCCCAGCCCAAGCCTCAGG A T ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:143382801..143383259 26863196 MeRIP-seq:(Medium) rs11978404 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_87395,Human_RBP_ID_794693,Human_RBP_ID_4929231,Human_RBP_ID_5134608,Human_RBP_ID_17092740,Human_RBP_ID_17315004,Human_RBP_ID_17427199,Human_RBP_ID_18959692,Human_RBP_ID_21396052,Human_RBP_ID_27106738 Human_miRNA_ID_1360781 71795 RMVar_ID_71795 Human_SNP_ID_343279352 m1A Human chr7 - 143382968 143382968 143382968 ACCTGAGGCTTGGGCTGGGGCTGGGGCTGAACATGGAACTGTGTCTGGCTCTGAGCCGGAGCCGG ACCTGAGGCTTGGGCTGGGGCTGGGGCTGAACTTGGAACTGTGTCTGGCTCTGAGCCGGAGCCGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143382803..143383150 26863196 MeRIP-seq:(Medium) rs780102608 Functional Loss SNV dbSNP153 33..33 33 - - - 71796 RMVar_ID_71796 Human_SNP_ID_343279449 m1A Human chr7 + 143383182 143383182 143383182 CCCCAGGTGGATCTGGGTCACAACCAAATCAAAAATTGGGGCACCCCGAAGCTCTTTCTGCTGGC CCCCAGGTGGATCTGGGTCACAACCAAATCAACAATTGGGGCACCCCGAAGCTCTTTCTGCTGGC A C ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:143382576..143383225 32194978 MeRIP-seq:(Medium) rs1333641305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1051024,Human_RBP_ID_18094876 71797 RMVar_ID_71797 Human_SNP_ID_343279466 m1A Human chr7 - 143383211 143383211 143383211 GTGAAGCTGGGAGGTTGAGGGGAGCCTGTGCCAGCAGAAAGAGCTTCGGGGTGCCCCAATTTTTG GTGAAGCTGGGAGGTTGAGGGGAGCCTGTGCCTGCAGAAAGAGCTTCGGGGTGCCCCAATTTTTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:143383165..143383325 26863196 MeRIP-seq:(Medium) rs1394797476 Functional Loss SNV dbSNP153 33..33 33 - - - 71798 RMVar_ID_71798 Human_SNP_ID_343279503 m1A Human chr7 + 143383288 143383288 143383288 GAGGGAGAAGCCCCGAGTGCAGGAGAAGCAGCACCCCGTGCCCCCACCGGCTCAGAACCAAAACC GAGGGAGAAGCCCCGAGTGCAGGAGAAGCAGCGCCCCGTGCCCCCACCGGCTCAGAACCAAAACC A G ZYX Ensembl:ENSG00000159840 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143383165..143383353 26863196 MeRIP-seq:(Medium) rs373067674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87396,Human_RBP_ID_8660612,Human_RBP_ID_17315006,Human_RBP_ID_17427466 Human_Splice_Rec_933097,Human_Splice_Rec_933121,Human_Splice_Rec_933137,Human_Splice_Rec_933149,Human_Splice_Rec_933155 71799 RMVar_ID_71799 Human_SNP_ID_343280266 m1A Human chr7 - 143385966 143385966 143385966 CATATACCATACCACACACACACACACCACTCACATTCAGATAATACCACACCAGGCCAGGCGCG CATATACCATACCACACACACACACACCACTCCCATTCAGATAATACCACACCAGGCCAGGCGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:143385961..143386667 26863196 MeRIP-seq:(Medium) rs1423965296 Functional Loss SNV dbSNP153 33..33 33 - - - 71800 RMVar_ID_71800 Human_SNP_ID_343280491 m1A Human chr7 - 143386751 143386751 143386751 TTATCTGCCTCTCCTCTTCCCCATCCACACCTACTACATGAACCCAGAAAAGCCTTAGTTGCCCC TTATCTGCCTCTCCTCTTCCCCATCCACACCTGCTACATGAACCCAGAAAAGCCTTAGTTGCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:143386748..143387357 26863196 MeRIP-seq:(Medium) rs1416154903 Functional Loss SNV dbSNP153 33..33 33 - - - 71801 RMVar_ID_71801 Human_SNP_ID_343280566 m1A Human chr7 - 143387140 143387140 143387140 GATCTTAGCCATTTTCCCTTAAGATCTTAGCCATCTTCCCTTAAGATCCTACCATCTCTTAACTG GATCTTAGCCATTTTCCCTTAAGATCTTAGCCGTCTTCCCTTAAGATCCTACCATCTCTTAACTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:143387132..143387322 26863196 MeRIP-seq:(Medium) rs1176656905 Functional Loss SNV dbSNP153 33..33 33 - - - 71802 RMVar_ID_71802 Human_SNP_ID_343281705 m1A Human chr7 + 143390904 143390901 143390904 TCTGGTCCTCGCCCATCCTGCAGGGATTGCCCACCGTCTTCCAGACACCCCACCTGAGGGGGGCA TCTGGTCCTCGCCCATCCTGCAGGGATTGC___CCGTCTTCCAGACACCCCACCTGAGGGGGGCA CCCA C ZYX Ensembl:ENSG00000159840 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143390557..143391002 26863196 MeRIP-seq:(Medium) rs1222279495 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_678115,Human_RBP_ID_5122925,Human_RBP_ID_17092742,Human_RBP_ID_17427203,Human_RBP_ID_17543299,Human_RBP_ID_17665483,Human_RBP_ID_18959699,Human_RBP_ID_27529186 Human_miRNA_ID_1705927 71803 RMVar_ID_71803 Human_SNP_ID_343429700 m1A Human chr7 + 144187278 144187278 144187278 CTGGCTCTTTCGCCTCCTGCCCGCTGACTGGGACCCCTTTCTCCTTTATACCATGATCTTCTTGC CTGGCTCTTTCGCCTCCTGCCCGCTGACTGGGTCCCCTTTCTCCTTTATACCATGATCTTCTTGC A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:144187239..144187317;chr7:144187230..144187571;chr7:144187231..144187348 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 71804 RMVar_ID_71804 Human_SNP_ID_344583746 m1A Human chr7 + 148698982 148698982 148698982 GACGGGGCTTTCGCCGGGGCCCAGGCCCAGGGACCAGGCGGAGGCGTCGCGGGAGCCTTTGGGGC GACGGGGCTTTCGCCGGGGCCCAGGCCCAGGGGCCAGGCGGAGGCGTCGCGGGAGCCTTTGGGGC A G CUL1 Ensembl:ENSG00000055130 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:148698791..148699050;chr7:148698518..148699075;chr7:148698780..148699111;chr7:148698815..148699009 26863196 MeRIP-seq:(Medium) rs1403622457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4929436,Human_RBP_ID_5328037,Human_RBP_ID_8914712,Human_RBP_ID_8944205,Human_RBP_ID_9338027,Human_RBP_ID_22464822,Human_RBP_ID_22730323,Human_RBP_ID_23080453 Human_Splice_Rec_934571,Human_Splice_Rec_934611,Human_Splice_Rec_934651,Human_Splice_Rec_934691,Human_Splice_Rec_934737,Human_Splice_Rec_934777,Human_Splice_Rec_934817,Human_Splice_Rec_934859,Human_Splice_Rec_934899,Human_Splice_Rec_934941 RMVar_hsa_circ_119100,RMVar_hsa_circ_249284 71805 RMVar_ID_71805 Human_SNP_ID_344583758 m1A Human chr7 + 148699015 148699015 148699015 CCAGGCGGAGGCGTCGCGGGAGCCTTTGGGGCACCACAGAGATGCGGGTGAGTGTCGGCAGCCGC CCAGGCGGAGGCGTCGCGGGAGCCTTTGGGGCGCCACAGAGATGCGGGTGAGTGTCGGCAGCCGC A G CUL1 Ensembl:ENSG00000055130 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:148698927..148730100 32194978 MeRIP-seq:(Medium) rs1484570768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956020,Human_RBP_ID_5328037,Human_RBP_ID_8944206,Human_RBP_ID_9312038,Human_RBP_ID_9337428,Human_RBP_ID_19021561,Human_RBP_ID_19135552,Human_RBP_ID_22464822,Human_RBP_ID_22730323,Human_RBP_ID_23080453,Human_RBP_ID_26793694 Human_Splice_Rec_934571,Human_Splice_Rec_934611,Human_Splice_Rec_934651,Human_Splice_Rec_934691,Human_Splice_Rec_934737,Human_Splice_Rec_934777,Human_Splice_Rec_934817,Human_Splice_Rec_934859,Human_Splice_Rec_934899,Human_Splice_Rec_934941 RMVar_hsa_circ_119100,RMVar_hsa_circ_249284 71806 RMVar_ID_71806 Human_SNP_ID_344583837 m1A Human chr7 + 148699181 148699181 148699181 GCGAGGCCTGAGCCGCCGAAACGCGGCCGGGCAGAATGGCGGCCGGGCCGGGGGACTCGTGGGCG GCGAGGCCTGAGCCGCCGAAACGCGGCCGGGCCGAATGGCGGCCGGGCCGGGGGACTCGTGGGCG A C CUL1 Ensembl:ENSG00000055130 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:148699173..148699292 26863196 MeRIP-seq:(Medium) rs1212119216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119100,RMVar_hsa_circ_249284 71807 RMVar_ID_71807 Human_SNP_ID_344622530 m1A Human chr7 + 148847277 148847277 148847277 ACGCTTCCGCCAACAAACTGGTCCCTTCTCAGATTTCTTCCCAGTCTGGCCCATGATTATTCTAA ACGCTTCCGCCAACAAACTGGTCCCTTCTCAGGTTTCTTCCCAGTCTGGCCCATGATTATTCTAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:148847226..148847375 26863196 MeRIP-seq:(Medium) rs1454209655 Functional Loss SNV dbSNP153 33..33 33 - - - 71808 RMVar_ID_71808 Human_SNP_ID_344622535 m1A Human chr7 - 148847298 148847296 148847299 TTTAATATGAAACCATTGCTTTTAGAATAATCATGGGCCAGACTGGGAAGAAATCTGAGAAGGGA TTTAATATGAAACCATTGCTTTTAGAATAAT___GGGCCAGACTGGGAAGAAATCTGAGAAGGGA CATG C EZH2 Ensembl:ENSG00000106462 Protein coding start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:148847276..148847350 26863410 MeRIP-seq:(Medium) rs1314292412 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3836599,Human_RBP_ID_4960959,Human_RBP_ID_7710251,Human_RBP_ID_16059671,Human_RBP_ID_18426113,Human_RBP_ID_19021573,Human_RBP_ID_24198531,Human_RBP_ID_26082226 Human_Splice_Rec_935044,Human_Splice_Rec_935080,Human_Splice_Rec_935120,Human_Splice_Rec_935156,Human_Splice_Rec_935194,Human_Splice_Rec_935230,Human_Splice_Rec_935266,Human_Splice_Rec_935306,Human_Splice_Rec_935324 RMVar_hsa_circ_96943,RMVar_hsa_circ_327932,RMVar_hsa_circ_50935,RMVar_hsa_circ_354172,RMVar_hsa_circ_371414,RMVar_hsa_circ_249305,RMVar_hsa_circ_366592,RMVar_hsa_circ_342673,RMVar_hsa_circ_249312,RMVar_hsa_circ_347200,RMVar_hsa_circ_272332,RMVar_hsa_circ_249318,RMVar_hsa_circ_357813,RMVar_hsa_circ_249317,RMVar_hsa_circ_302655,RMVar_hsa_circ_249319,RMVar_hsa_circ_367884,RMVar_hsa_circ_285103,RMVar_hsa_circ_249322,RMVar_hsa_circ_249323,RMVar_hsa_circ_84815,RMVar_hsa_circ_274393,RMVar_hsa_circ_274419,RMVar_hsa_circ_249325,RMVar_hsa_circ_249326,RMVar_hsa_circ_280782,RMVar_hsa_circ_249328,RMVar_hsa_circ_79673,RMVar_hsa_circ_249327 71809 RMVar_ID_71809 Human_SNP_ID_344632944 m1A Human chr7 - 148884246 148884245 148884247 TCCGGTCGCGTCCGACACCCGGTGGGACTCAGAAGGCAGTGGAGCCCCGGCGGCGGCGGCGGCGG TCCGGTCGCGTCCGACACCCGGTGGGACTCA__AGGCAGTGGAGCCCCGGCGGCGGCGGCGGCGG TTC T EZH2 Ensembl:ENSG00000106462 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:148883468..148884275 26863196 MeRIP-seq:(Medium) rs1273478866 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4929613,Human_RBP_ID_18426451,Human_RBP_ID_18451283,Human_RBP_ID_23080194 Human_Splice_Rec_935043,Human_Splice_Rec_935079,Human_Splice_Rec_935155,Human_Splice_Rec_935193,Human_Splice_Rec_935265,Human_Splice_Rec_935305,Human_Splice_Rec_935323 71810 RMVar_ID_71810 Human_SNP_ID_344632945 m1A Human chr7 - 148884246 148884246 148884246 TCCGGTCGCGTCCGACACCCGGTGGGACTCAGAAGGCAGTGGAGCCCCGGCGGCGGCGGCGGCGG TCCGGTCGCGTCCGACACCCGGTGGGACTCAGCAGGCAGTGGAGCCCCGGCGGCGGCGGCGGCGG T G EZH2 Ensembl:ENSG00000106462 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:148883468..148884275 26863196 MeRIP-seq:(Medium) rs1215160919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4929613,Human_RBP_ID_18426451,Human_RBP_ID_18451283,Human_RBP_ID_23080194 Human_Splice_Rec_935043,Human_Splice_Rec_935079,Human_Splice_Rec_935155,Human_Splice_Rec_935193,Human_Splice_Rec_935265,Human_Splice_Rec_935305,Human_Splice_Rec_935323 71811 RMVar_ID_71811 Human_SNP_ID_344665267 m1A Human chr7 - 149005261 149005261 149005261 ACTATGCTGGGGAGGTGAAGGACCTGGGGCTCAGCGAGAGTGGGGAGGATGTCAATGCCGCCATC ACTATGCTGGGGAGGTGAAGGACCTGGGGCTCCGCGAGAGTGGGGAGGATGTCAATGCCGCCATC T G PDIA4 Ensembl:ENSG00000155660 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149005098..149005313 26863196 MeRIP-seq:(Medium) rs758170854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85222,Human_RBP_ID_678351,Human_RBP_ID_793654,Human_RBP_ID_956965,Human_RBP_ID_2037431,Human_RBP_ID_7710729,Human_RBP_ID_9263566,Human_RBP_ID_9404038,Human_RBP_ID_9444389,Human_RBP_ID_16061501,Human_RBP_ID_18108243,Human_RBP_ID_18196411,Human_RBP_ID_18877949,Human_RBP_ID_19029407,Human_RBP_ID_22463799,Human_RBP_ID_22774534,Human_RBP_ID_24198733,Human_RBP_ID_26357249,Human_RBP_ID_27107008,Human_RBP_ID_27353223 RMVar_hsa_circ_84538,RMVar_hsa_circ_104864,RMVar_hsa_circ_249331,RMVar_hsa_circ_249332,RMVar_hsa_circ_268039 71812 RMVar_ID_71812 Human_SNP_ID_344669863 m1A Human chr7 - 149021108 149021108 149021108 TAACAGAGAAAATGCCATTGAGGATGAAGAGGAGGAGGAGGAGGAAGATGATGATGAGGAAGAAG TAACAGAGAAAATGCCATTGAGGATGAAGAGGCGGAGGAGGAGGAAGATGATGATGAGGAAGAAG T G PDIA4 Ensembl:ENSG00000155660 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149021057..149021201 26863196 MeRIP-seq:(Medium) rs139617230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793660,Human_RBP_ID_843944,Human_RBP_ID_955048,Human_RBP_ID_1683305,Human_RBP_ID_2037448,Human_RBP_ID_3070246,Human_RBP_ID_3836736,Human_RBP_ID_4929746,Human_RBP_ID_7710755,Human_RBP_ID_8271834,Human_RBP_ID_8944208,Human_RBP_ID_9404058,Human_RBP_ID_18095162,Human_RBP_ID_18451289,Human_RBP_ID_18472402,Human_RBP_ID_18540120,Human_RBP_ID_18877958,Human_RBP_ID_22112667,Human_RBP_ID_22833831,Human_RBP_ID_23080195,Human_RBP_ID_23116865,Human_RBP_ID_23120522,Human_RBP_ID_24198779,Human_RBP_ID_24549169,Human_RBP_ID_26357260,Human_RBP_ID_27107052,Human_RBP_ID_27829967 Human_Splice_Rec_935346,Human_Splice_Rec_935364,Human_Splice_Rec_935388 RMVar_hsa_circ_371845,RMVar_hsa_circ_360788,RMVar_hsa_circ_249333,RMVar_hsa_circ_276510,RMVar_hsa_circ_356601,RMVar_hsa_circ_249338,RMVar_hsa_circ_249339,RMVar_hsa_circ_85051 71813 RMVar_ID_71813 Human_SNP_ID_344671995 m1A Human chr7 - 149028310 149028310 149028310 GGTGCCGAGGGCCCGGACGAGGGTGAGCGGCAAGCGCGCCGCGGGTCGGGCTGTGCTTGCGGGGG GGTGCCGAGGGCCCGGACGAGGGTGAGCGGCAGGCGCGCCGCGGGTCGGGCTGTGCTTGCGGGGG T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:149028301..149028569 26863196 MeRIP-seq:(Medium) rs1024036509 Functional Loss SNV dbSNP153 33..33 33 - - - 71814 RMVar_ID_71814 Human_SNP_ID_344700414 m1A Human chr7 - 149126251 149126251 149126251 CCTGGGAGTTGGGTTGGGGCGGAGCGGAGGGGAGGCCGTGCCAGGCAGGGCCGGTTCGTGCGGAA CCTGGGAGTTGGGTTGGGGCGGAGCGGAGGGGGGGCCGTGCCAGGCAGGGCCGGTTCGTGCGGAA T C ZNF425 Ensembl:ENSG00000204947 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149126036..149126261 26863196 MeRIP-seq:(Medium) rs765329184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3864393,Human_RBP_ID_9439409,Human_RBP_ID_18426117 Human_Splice_Rec_935401 71815 RMVar_ID_71815 Human_SNP_ID_344706064 m1A Human chr7 - 149147534 149147534 149147534 ACGCGGCGGAGGCGCGGTGCAGCAGGCGGCGGATCAAGCTGGGGTCGCGAGGCCGACTCCGCCGC ACGCGGCGGAGGCGCGGTGCAGCAGGCGGCGGGTCAAGCTGGGGTCGCGAGGCCGACTCCGCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:149147484..149147819;chr7:149147489..149147790 26863196 MeRIP-seq:(Medium) rs868385291 Functional Loss SNV dbSNP153 33..33 33 - - - 71816 RMVar_ID_71816 Human_SNP_ID_344706065 m1A Human chr7 - 149147534 149147534 149147534 ACGCGGCGGAGGCGCGGTGCAGCAGGCGGCGGATCAAGCTGGGGTCGCGAGGCCGACTCCGCCGC ACGCGGCGGAGGCGCGGTGCAGCAGGCGGCGGCTCAAGCTGGGGTCGCGAGGCCGACTCCGCCGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:149147484..149147819;chr7:149147489..149147790 26863196 MeRIP-seq:(Medium) rs868385291 Functional Loss SNV dbSNP153 33..33 33 - - - 71817 RMVar_ID_71817 Human_SNP_ID_344706083 m1A Human chr7 + 149147588 149147588 149147588 CTCCGCCGCGTTCCTGCGCGTCCCGAGCCCCGACGGCCGCGTGAGTCCCGTCCGTGCGGGGAAGG CTCCGCCGCGTTCCTGCGCGTCCCGAGCCCCGGCGGCCGCGTGAGTCCCGTCCGTGCGGGGAAGG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:149147501..149147594 26863410 MeRIP-seq:(Medium) rs1314999578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337437 71818 RMVar_ID_71818 Human_SNP_ID_344707727 m1A Human chr7 + 149153894 149153894 149153894 AAGCAGTCCTTATCTGATTTTAGTTTGGAGTTAGGGTTCCTTCTAACACTCAATGTCTTGTTCCA AAGCAGTCCTTATCTGATTTTAGTTTGGAGTTGGGGTTCCTTCTAACACTCAATGTCTTGTTCCA A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149153893..149153979 26863196 MeRIP-seq:(Medium) rs765135082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22686055 71819 RMVar_ID_71819 Human_SNP_ID_344707761 m1A Human chr7 - 149153995 149153995 149153995 AGGTGTGCCTCATTTGCTGCTGGGGGTGTAGGAAGAGGAAGGGGCTGCAGGGATGTAAGGCACTC AGGTGTGCCTCATTTGCTGCTGGGGGTGTAGGGAGAGGAAGGGGCTGCAGGGATGTAAGGCACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149153929..149153997 26863196 MeRIP-seq:(Medium) rs770573642 Functional Loss SNV dbSNP153 33..33 33 - - - 71820 RMVar_ID_71820 Human_SNP_ID_344709195 m1A Human chr7 + 149158096 149158090 149158096 AGAGCAAGACTCCGTCTCCAAAAAACGAATAAAAATAAAAATCAAAAAGAAGGAAAGGCTGATGA AGAGCAAGACTCCGTCTCCAAAAAACG______AATAAAAATCAAAAAGAAGGAAAGGCTGATGA GAATAAA G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149158094..149158248 26863196 MeRIP-seq:(Medium) rs1462160644 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_249343,RMVar_hsa_circ_274325,RMVar_hsa_circ_304748,RMVar_hsa_circ_91132,RMVar_hsa_circ_249342 71821 RMVar_ID_71821 Human_SNP_ID_344709212 m1A Human chr7 + 149158144 149158144 149158144 GAAGGAAAGGCTGATGAGGTAGAGGAAAAAACAAACAGGAAAGTATGTGGTGTCACAGGGCCAAG GAAGGAAAGGCTGATGAGGTAGAGGAAAAAACCAACAGGAAAGTATGTGGTGTCACAGGGCCAAG A C ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149158108..149158245 26863196 MeRIP-seq:(Medium) rs991918305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249343,RMVar_hsa_circ_274325,RMVar_hsa_circ_304748,RMVar_hsa_circ_91132,RMVar_hsa_circ_249342 71822 RMVar_ID_71822 Human_SNP_ID_344709213 m1A Human chr7 + 149158144 149158144 149158144 GAAGGAAAGGCTGATGAGGTAGAGGAAAAAACAAACAGGAAAGTATGTGGTGTCACAGGGCCAAG GAAGGAAAGGCTGATGAGGTAGAGGAAAAAACGAACAGGAAAGTATGTGGTGTCACAGGGCCAAG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149158108..149158245 26863196 MeRIP-seq:(Medium) rs991918305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249343,RMVar_hsa_circ_274325,RMVar_hsa_circ_304748,RMVar_hsa_circ_91132,RMVar_hsa_circ_249342 71823 RMVar_ID_71823 Human_SNP_ID_344714650 m1A Human chr7 + 149179088 149179088 149179088 AGACACCCCCCACCTGCCCACACTGTGCCAGGACTTTTACTCACCCATCAAGACTTACCTACCAT AGACACCCCCCACCTGCCCACACTGTGCCAGGGCTTTTACTCACCCATCAAGACTTACCTACCAT A G ZNF398 Ensembl:ENSG00000197024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149179038..149179103 26863196 MeRIP-seq:(Medium) rs1420323152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16062455,Human_RBP_ID_17312183,Human_RBP_ID_17424732,Human_RBP_ID_18451293,Human_RBP_ID_18540121,Human_RBP_ID_27353290,Human_RBP_ID_27529315 71824 RMVar_ID_71824 Human_SNP_ID_344724525 m1A Human chr7 + 149217697 149217697 149217697 CTCTGAGAACAATGGCAGGGAGAACAGGAAGGAGTGTGGACATGAGGCAGAGCAAAGACAGAGTG CTCTGAGAACAATGGCAGGGAGAACAGGAAGGGGTGTGGACATGAGGCAGAGCAAAGACAGAGTG A G ZNF282 Ensembl:ENSG00000170265 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149217694..149217933 26863196 MeRIP-seq:(Medium) rs78755455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7711080,Human_RBP_ID_16063390 71825 RMVar_ID_71825 Human_SNP_ID_344724707 m1A Human chr7 - 149218276 149218276 149218276 TCCTTTCTCTCCCTGTGCACTGCTGCTACCCCAGCTCTGACCACCAGCATCTCTCCACTTGGTCT TCCTTTCTCTCCCTGTGCACTGCTGCTACCCCCGCTCTGACCACCAGCATCTCTCCACTTGGTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149218272..149218434 26863196 MeRIP-seq:(Medium) rs769424300 Functional Loss SNV dbSNP153 33..33 33 - - - 71826 RMVar_ID_71826 Human_SNP_ID_344726705 m1A Human chr7 + 149225098 149225098 149225098 CCTTCATGATGACAACACTGCCTCGCGTTTCAATAGCGCTTTATACTTTTTTAAGTGTTTTCTAT CCTTCATGATGACAACACTGCCTCGCGTTTCAGTAGCGCTTTATACTTTTTTAAGTGTTTTCTAT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs777172268 Functional Loss SNV dbSNP153 33..33 33 - - - 71827 RMVar_ID_71827 Human_SNP_ID_344726967 m1A Human chr7 + 149226045 149226039 149226046 CCTCCCAGCCGGGATCACAGTGGGCAGCCGGCACCCGGCACCACTTTGGCGAGCGTCCTGCTTCC CCTCCCAGCCGGGATCACAGTGGGCAG_______CCGGCACCACTTTGGCGAGCGTCCTGCTTCC GCCGGCAC G ZNF282 Ensembl:ENSG00000170265 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149226000..149226087 26863196 MeRIP-seq:(Medium) rs1342078831 Functional Loss DEL dbSNP153 28..34 33 - - - Human_miRNA_ID_2845677,Human_miRNA_ID_2848698 71828 RMVar_ID_71828 Human_SNP_ID_344733472 m1A Human chr7 - 149250369 149250369 149250369 CTGGTTCCCGAACTCCACGGCCATCTTCTCGCAGTCAGCCAGCTTCTTCTCGGCTGTCCCCGTGC CTGGTTCCCGAACTCCACGGCCATCTTCTCGCTGTCAGCCAGCTTCTTCTCGGCTGTCCCCGTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149250319..149250426 26863196 MeRIP-seq:(Medium) rs1414005317 Functional Loss SNV dbSNP153 33..33 33 - - - 71829 RMVar_ID_71829 Human_SNP_ID_344738411 m1A Human chr7 + 149266621 149266621 149266621 GGGCAAGTGGGCCGTGCTGGGGACCTTGCTGCAGGAGTACGGGCTGCTGCAGAGGCGGCTGGAGA GGGCAAGTGGGCCGTGCTGGGGACCTTGCTGCGGGAGTACGGGCTGCTGCAGAGGCGGCTGGAGA A G ZNF783 Ensembl:ENSG00000204946 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:149262260..149278492 32194978 MeRIP-seq:(Medium) rs776911206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9404061,Human_RBP_ID_19020240 RMVar_hsa_circ_46074,RMVar_hsa_circ_111713,RMVar_hsa_circ_302274,RMVar_hsa_circ_347241,RMVar_hsa_circ_249353,RMVar_hsa_circ_317080,RMVar_hsa_circ_96115,RMVar_hsa_circ_249355,RMVar_hsa_circ_249356,RMVar_hsa_circ_249354 71830 RMVar_ID_71830 Human_SNP_ID_344738412 m1A Human chr7 + 149266624 149266624 149266624 CAAGTGGGCCGTGCTGGGGACCTTGCTGCAGGAGTACGGGCTGCTGCAGAGGCGGCTGGAGAATG CAAGTGGGCCGTGCTGGGGACCTTGCTGCAGGCGTACGGGCTGCTGCAGAGGCGGCTGGAGAATG A C ZNF783 Ensembl:ENSG00000204946 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149266458..149266726 26863196 MeRIP-seq:(Medium) rs201372254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9404061,Human_RBP_ID_19020240 RMVar_hsa_circ_46074,RMVar_hsa_circ_111713,RMVar_hsa_circ_302274,RMVar_hsa_circ_347241,RMVar_hsa_circ_249353,RMVar_hsa_circ_317080,RMVar_hsa_circ_96115,RMVar_hsa_circ_249355,RMVar_hsa_circ_249356,RMVar_hsa_circ_249354 71831 RMVar_ID_71831 Human_SNP_ID_344738531 m1A Human chr7 + 149266865 149266865 149266865 CGATGATGTGGCCGTGTATTTCTCTGAGCTGGAGTGGGGCAAGCTGGAGGACTGGCAGAAGGAGC CGATGATGTGGCCGTGTATTTCTCTGAGCTGGGGTGGGGCAAGCTGGAGGACTGGCAGAAGGAGC A G ZNF783 Ensembl:ENSG00000204946 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149266738..149266879 26863196 MeRIP-seq:(Medium) rs1386338957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021582,Human_RBP_ID_22318921 Human_Splice_Rec_935530,Human_Splice_Rec_935531,Human_Splice_Rec_935554,Human_Splice_Rec_935555,Human_Splice_Rec_935564,Human_Splice_Rec_935565 RMVar_hsa_circ_46074,RMVar_hsa_circ_111713,RMVar_hsa_circ_302274,RMVar_hsa_circ_347241,RMVar_hsa_circ_249353,RMVar_hsa_circ_317080,RMVar_hsa_circ_96115,RMVar_hsa_circ_249355,RMVar_hsa_circ_249356,RMVar_hsa_circ_249354 71832 RMVar_ID_71832 Human_SNP_ID_344744509 m1A Human chr7 - 149288422 149288422 149288422 CGTGTCTTCAGGAGTCACAGGCACCTGGAAGTACAAGTTGCCTGCACCCACCATGAATAACAACC CGTGTCTTCAGGAGTCACAGGCACCTGGAAGTGCAAGTTGCCTGCACCCACCATGAATAACAACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149288387..149288478 26863196 MeRIP-seq:(Medium) rs146919862 Functional Loss SNV dbSNP153 33..33 33 - - - 71833 RMVar_ID_71833 Human_SNP_ID_344754912 m1A Human chr7 + 149331184 149331184 149331184 CATTTGACTGCAGATCAAGAGGTCCCTGGTTCAAATCCAGGTGCCCCCTACTCCTTTTAATCACT CATTTGACTGCAGATCAAGAGGTCCCTGGTTCGAATCCAGGTGCCCCCTACTCCTTTTAATCACT A G tRNA-Cys-GCA-9-1 RNACentral:URS00003A8311 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs923416308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1683385,Human_RBP_ID_5269404,Human_RBP_ID_5512815,Human_RBP_ID_5628200,Human_RBP_ID_8661646,Human_RBP_ID_18095307,Human_RBP_ID_21953310,Human_RBP_ID_22835930,Human_RBP_ID_23139728 71834 RMVar_ID_71834 Human_SNP_ID_344780729 m1A Human chr7 - 149431675 149431675 149431675 CGAGCCCAGCGGGCGGGGGCGGGGCGCCCCCCAGCCCCTTTGCCGTGAGCTCCCCCTCTCCTCTC CGAGCCCAGCGGGCGGGGGCGGGGCGCCCCCCGGCCCCTTTGCCGTGAGCTCCCCCTCTCCTCTC T C ZNF777 Ensembl:ENSG00000196453 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149431632..149431723 26863196 MeRIP-seq:(Medium) rs1333344520 Functional Loss SNV dbSNP153 33..33 33 - - - 71835 RMVar_ID_71835 Human_SNP_ID_344780790 m1A Human chr7 + 149431733 149431733 149431733 GGGCTCGGGCCTGGCGGTGTCCGAGGGGGGGCACGGCCCGCGCACCTGGCCGGGCGGCGGCGGCG GGGCTCGGGCCTGGCGGTGTCCGAGGGGGGGCGCGGCCCGCGCACCTGGCCGGGCGGCGGCGGCG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:149431668..149431767 26863410 MeRIP-seq:(Medium) rs1484289013 Functional Loss SNV dbSNP153 33..33 33 - - - 71836 RMVar_ID_71836 Human_SNP_ID_344787058 m1A Human chr7 - 149455645 149455645 149455645 TCCCTTCTCTCCCACTCCCCCCACCACCAGGAAGCCCCCGTTCACTCCCCTGAAGCTCCTGAGAA TCCCTTCTCTCCCACTCCCCCCACCACCAGGAGGCCCCCGTTCACTCCCCTGAAGCTCCTGAGAA T C ZNF777 Ensembl:ENSG00000196453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149455594..149455768 26863196 MeRIP-seq:(Medium) rs566343111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18959710,Human_RBP_ID_27529403 RMVar_hsa_circ_280120 71837 RMVar_ID_71837 Human_SNP_ID_344787108 m1A Human chr7 + 149455750 149455750 149455750 CCTTCCTGGGAAGCCAGGGGGCCCTGGAGAGAAGTCTCTTGCTCAGAAGCGGCAGAACACAGGAG CCTTCCTGGGAAGCCAGGGGGCCCTGGAGAGACGTCTCTTGCTCAGAAGCGGCAGAACACAGGAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:149455699..149455799 32194978 MeRIP-seq:(Medium) rs1198281896 Functional Loss SNV dbSNP153 33..33 33 - - - 71838 RMVar_ID_71838 Human_SNP_ID_344787109 m1A Human chr7 + 149455750 149455750 149455750 CCTTCCTGGGAAGCCAGGGGGCCCTGGAGAGAAGTCTCTTGCTCAGAAGCGGCAGAACACAGGAG CCTTCCTGGGAAGCCAGGGGGCCCTGGAGAGAGGTCTCTTGCTCAGAAGCGGCAGAACACAGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:149455699..149455799 32194978 MeRIP-seq:(Medium) rs1198281896 Functional Loss SNV dbSNP153 33..33 33 - - - 71839 RMVar_ID_71839 Human_SNP_ID_344787159 m1A Human chr7 + 149455912 149455912 149455912 GGAGACAAAGAAGGAATTTCTTTGGGAGGAAGAACGCGGGATTGGAACAGAGTTTCTCGGGGGAG GGAGACAAAGAAGGAATTTCTTTGGGAGGAAGTACGCGGGATTGGAACAGAGTTTCTCGGGGGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149455861..149456042 26863196 MeRIP-seq:(Medium) rs960389840 Functional Loss SNV dbSNP153 33..33 33 - - - 71840 RMVar_ID_71840 Human_SNP_ID_344787192 m1A Human chr7 - 149455978 149455978 149455978 CGCTCATCACCTCTGTCGTTCCCCAGTGTTCCACAAGAAGAAACCTTACGTCAGGCCCCTGCTGG CGCTCATCACCTCTGTCGTTCCCCAGTGTTCCGCAAGAAGAAACCTTACGTCAGGCCCCTGCTGG T C ZNF777 Ensembl:ENSG00000196453 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:149455878..149456004 26863196 MeRIP-seq:(Medium) rs758029128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_935648 RMVar_hsa_circ_280120 71841 RMVar_ID_71841 Human_SNP_ID_344791385 m1A Human chr7 - 149472873 149472873 149472873 GTTTCTATGTACTGTATATTTTGTACCTGTTTACACTTCTAATATTGATATAACTGATATTTTGA GTTTCTATGTACTGTATATTTTGTACCTGTTTCCACTTCTAATATTGATATAACTGATATTTTGA T G ZNF746 Ensembl:ENSG00000181220 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:149472843..149472943 32194978 MeRIP-seq:(Medium) rs1563245584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4930198,Human_RBP_ID_5153331,Human_RBP_ID_21903659,Human_RBP_ID_24437999,Human_RBP_ID_27529411 Human_miRNA_ID_799648,Human_miRNA_ID_803749,Human_miRNA_ID_807857,Human_miRNA_ID_811955,Human_miRNA_ID_816058,Human_miRNA_ID_2334919,Human_miRNA_ID_2337152,Human_miRNA_ID_2339383,Human_miRNA_ID_2341621,Human_miRNA_ID_2343856 RMVar_hsa_circ_106929,RMVar_hsa_circ_249359 71842 RMVar_ID_71842 Human_SNP_ID_344792065 m1A Human chr7 + 149474843 149474843 149474843 CTGCCCCCACCGCTGCCGCCACCGCCGCCGCCACTGCCGCTGCCGCCACCGCCTGTGCCCGGGCC CTGCCCCCACCGCTGCCGCCACCGCCGCCGCCGCTGCCGCTGCCGCCACCGCCTGTGCCCGGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:149474371..149475001;chr7:149474534..149475035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 71843 RMVar_ID_71843 Human_SNP_ID_344792162 m1A Human chr7 - 149475023 149475023 149475023 AACGAACCCTGTAAATACCCTGGCCGGACCAAAGGCTTTGGCCACAAGCCAGGGCTGAAGAAGCA AACGAACCCTGTAAATACCCTGGCCGGACCAAGGGCTTTGGCCACAAGCCAGGGCTGAAGAAGCA T C ZNF746 Ensembl:ENSG00000181220 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149474982..149475083 26863196 MeRIP-seq:(Medium) rs900641661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1051128,Human_RBP_ID_8909325,Human_RBP_ID_21904245,Human_RBP_ID_27107393,Human_RBP_ID_27529432,Human_RBP_ID_27568949 Human_miRNA_ID_2034045,Human_miRNA_ID_2035349,Human_miRNA_ID_3106976 RMVar_hsa_circ_106929,RMVar_hsa_circ_249359 71844 RMVar_ID_71844 Human_SNP_ID_344793067 m1A Human chr7 + 149477601 149477601 149477601 GTGGCATCCGTGGAGATGTCTCCTGCTCCGGAATCCAGCTGGCTGAGGCCCCAGGGCTCCTCCCC GTGGCATCCGTGGAGATGTCTCCTGCTCCGGATTCCAGCTGGCTGAGGCCCCAGGGCTCCTCCCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:149477017..149477783 32194978 MeRIP-seq:(Medium) rs764339273 Functional Loss SNV dbSNP153 33..33 33 - - - 71845 RMVar_ID_71845 Human_SNP_ID_344798119 m1A Human chr7 - 149497510 149497510 149497510 AGGGCCATGGCCGAGGCGGTCGCGGCTCCGGTAAGGGCGACCCGCGCGCGCAGGGACTCGCGGCC AGGGCCATGGCCGAGGCGGTCGCGGCTCCGGTTAGGGCGACCCGCGCGCGCAGGGACTCGCGGCC T A ZNF746 Ensembl:ENSG00000181220 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:149497503..149497691 26863196 MeRIP-seq:(Medium) rs1213065914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955060 RMVar_hsa_circ_106929,RMVar_hsa_circ_249359,RMVar_hsa_circ_249362 71846 RMVar_ID_71846 Human_SNP_ID_344798155 m1A Human chr7 - 149497576 149497576 149497576 GGGCCTGCGTGGTGCCGCGCGCGGCGGCGGCGACGACGACTTCCTCCGGGCCGGGCGGGACAGCG GGGCCTGCGTGGTGCCGCGCGCGGCGGCGGCGGCGACGACTTCCTCCGGGCCGGGCGGGACAGCG T C ZNF746 Ensembl:ENSG00000181220 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:149497501..149497704 26863196 MeRIP-seq:(Medium) rs941784239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955060,Human_RBP_ID_4930263,Human_RBP_ID_23080196 Human_Splice_Rec_935657,Human_Splice_Rec_935669,Human_Splice_Rec_935681,Human_Splice_Rec_935697 RMVar_hsa_circ_106929,RMVar_hsa_circ_249359,RMVar_hsa_circ_249362 71847 RMVar_ID_71847 Human_SNP_ID_344809433 m1A Human chr7 - 149548345 149548343 149548345 CAGGGAAGAAATGTAACTACATGTGGGAAAACAGGGATTAACGAGGGGCAAGGAAGAGGAGTTGG CAGGGAAGAAATGTAACTACATGTGGGAAAAC__GGATTAACGAGGGGCAAGGAAGAGGAGTTGG CCT C ZNF767P Ensembl:ENSG00000133624 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149548294..149548396 26863196 MeRIP-seq:(Medium) rs1288128198 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_88550,RMVar_hsa_circ_249362,RMVar_hsa_circ_249365,RMVar_hsa_circ_249364 71848 RMVar_ID_71848 Human_SNP_ID_344809435 m1A Human chr7 - 149548345 149548345 149548345 CAGGGAAGAAATGTAACTACATGTGGGAAAACAGGGATTAACGAGGGGCAAGGAAGAGGAGTTGG CAGGGAAGAAATGTAACTACATGTGGGAAAACCGGGATTAACGAGGGGCAAGGAAGAGGAGTTGG T G ZNF767P Ensembl:ENSG00000133624 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149548294..149548396 26863196 MeRIP-seq:(Medium) rs887415414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88550,RMVar_hsa_circ_249362,RMVar_hsa_circ_249365,RMVar_hsa_circ_249364 71849 RMVar_ID_71849 Human_SNP_ID_344810799 m1A Human chr7 - 149553522 149553521 149553522 TGGAAAGGGAGGGAGACCGTGGAAAGAGAGGGAGAGGGAGACCGTGGGGAGAGGGAGACCGAGAG TGGAAAGGGAGGGAGACCGTGGAAAGAGAGGG_GAGGGAGACCGTGGGGAGAGGGAGACCGAGAG CT C ZNF767P Ensembl:ENSG00000133624 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149553474..149553642 26863196 MeRIP-seq:(Medium) rs1205830598 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_249362,RMVar_hsa_circ_249366,RMVar_hsa_circ_249367,RMVar_hsa_circ_274154,RMVar_hsa_circ_249373,RMVar_hsa_circ_249374,RMVar_hsa_circ_282044 71850 RMVar_ID_71850 Human_SNP_ID_344811005 m1A Human chr7 + 149554015 149554015 149554015 GAGCGTCTCTGCCCGGCCACCCATCGTCTGGGACGTGAGGAGCCCCTCTGCCTGTCTGCCCAGTC GAGCGTCTCTGCCCGGCCACCCATCGTCTGGGGCGTGAGGAGCCCCTCTGCCTGTCTGCCCAGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149554008..149554116 26863196 MeRIP-seq:(Medium) rs1326955479 Functional Loss SNV dbSNP153 33..33 33 - - - 71851 RMVar_ID_71851 Human_SNP_ID_344820532 m1A Human chr7 - 149589158 149589158 149589158 ATGGCCATACAGGTTTATAGTAGTTATTAGAGATAGGTAGTCAAATGGGGGTATAGCTCAGGGGT ATGGCCATACAGGTTTATAGTAGTTATTAGAGTTAGGTAGTCAAATGGGGGTATAGCTCAGGGGT T A ZNF767P Ensembl:ENSG00000133624 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149589156..149589280 26863196 MeRIP-seq:(Medium) rs553196388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8944399 RMVar_hsa_circ_249366,RMVar_hsa_circ_249375 71852 RMVar_ID_71852 Human_SNP_ID_344820533 m1A Human chr7 - 149589158 149589158 149589158 ATGGCCATACAGGTTTATAGTAGTTATTAGAGATAGGTAGTCAAATGGGGGTATAGCTCAGGGGT ATGGCCATACAGGTTTATAGTAGTTATTAGAGCTAGGTAGTCAAATGGGGGTATAGCTCAGGGGT T G ZNF767P Ensembl:ENSG00000133624 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149589156..149589280 26863196 MeRIP-seq:(Medium) rs553196388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8944399 RMVar_hsa_circ_249366,RMVar_hsa_circ_249375 71853 RMVar_ID_71853 Human_SNP_ID_344824931 m1A Human chr7 - 149606038 149606038 149606038 GAGAGAGGAGAAGCATGGAGAGATGGTGGAGGAGCTGGAGTTTGGGGGCAACGTGGAGAACGAGG GAGAGAGGAGAAGCATGGAGAGATGGTGGAGGGGCTGGAGTTTGGGGGCAACGTGGAGAACGAGG T C ZNF767P Ensembl:ENSG00000133624 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:149605797..149606134 26863196 MeRIP-seq:(Medium) rs953975428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5104948,Human_RBP_ID_7711581,Human_RBP_ID_9439920,Human_RBP_ID_22529171,Human_RBP_ID_22730328,Human_RBP_ID_23120524,Human_RBP_ID_26357273 71854 RMVar_ID_71854 Human_SNP_ID_344827115 m1A Human chr7 + 149614284 149614284 149614284 AGAGCTGGAAGCTTCCTCTCTCCTTCTCTCCTACTTTAGTTTTATCTTCTCTTACCTACATCCCA AGAGCTGGAAGCTTCCTCTCTCCTTCTCTCCTGCTTTAGTTTTATCTTCTCTTACCTACATCCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149614279..149614378 26863196 MeRIP-seq:(Medium) rs534970191 Functional Loss SNV dbSNP153 33..33 33 - - - 71855 RMVar_ID_71855 Human_SNP_ID_344827649 m1A Human chr7 + 149616158 149616155 149616158 TAGGGTTTCTGGTGGAGTGGATGCGGATGTGGAGGAGGAGGTCAGAGAGGACTCGTGGGGTTTTG TAGGGTTTCTGGTGGAGTGGATGCGGATGT___GGAGGAGGTCAGAGAGGACTCGTGGGGTTTTG TGGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149616156..149616308 26863196 MeRIP-seq:(Medium) rs937849824 Functional Loss DEL dbSNP153 31..33 33 - - - 71856 RMVar_ID_71856 Human_SNP_ID_344830331 m1A Human chr7 - 149624690 149624690 149624690 CGGGCGGCGCAGGGCAGGGGCAGTCAGGGAGCAGCGGCGGCAGAGACAGGGCTGGGCGGGCGCCG CGGGCGGCGCAGGGCAGGGGCAGTCAGGGAGCCGCGGCGGCAGAGACAGGGCTGGGCGGGCGCCG T G ZNF767P Ensembl:ENSG00000133624 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149621521..149624750 26863196 MeRIP-seq:(Medium) rs994017901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795186,Human_RBP_ID_8273020,Human_RBP_ID_17672260,Human_RBP_ID_18426456 71857 RMVar_ID_71857 Human_SNP_ID_344845894 m1A Human chr7 + 149691260 149691260 149691260 TGCTCTACCCCTGAGCTATATCCCCATGGGCCACAAAGTTTTCCAGCTGGCATTATTTCATGGTG TGCTCTACCCCTGAGCTATATCCCCATGGGCCCCAAAGTTTTCCAGCTGGCATTATTTCATGGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149691103..149691281 26863196 MeRIP-seq:(Medium) rs372449576 Functional Loss SNV dbSNP153 33..33 33 - - - 71858 RMVar_ID_71858 Human_SNP_ID_344845895 m1A Human chr7 + 149691260 149691260 149691260 TGCTCTACCCCTGAGCTATATCCCCATGGGCCACAAAGTTTTCCAGCTGGCATTATTTCATGGTG TGCTCTACCCCTGAGCTATATCCCCATGGGCCGCAAAGTTTTCCAGCTGGCATTATTTCATGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149691103..149691281 26863196 MeRIP-seq:(Medium) rs372449576 Functional Loss SNV dbSNP153 33..33 33 - - - 71859 RMVar_ID_71859 Human_SNP_ID_344852780 m1A Human chr7 - 149719625 149719625 149719625 TCTCGTAGTTCTCCCGCATCACGTCTCGGTAGAACTCCCTCTGCCCCTCCTCCAGGAGCCGCCAC TCTCGTAGTTCTCCCGCATCACGTCTCGGTAGCACTCCCTCTGCCCCTCCTCCAGGAGCCGCCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149719534..149719707 26863196 MeRIP-seq:(Medium) rs762655306 Functional Loss SNV dbSNP153 33..33 33 - - - 71860 RMVar_ID_71860 Human_SNP_ID_344853194 m1A Human chr7 + 149720933 149720933 149720933 TCTTGTTTGGAGAAGTCAAGGGCGCTATGGACAGCCCCGAGAGCGAGAGCCGGGGAGCCAGCCTG TCTTGTTTGGAGAAGTCAAGGGCGCTATGGACGGCCCCGAGAGCGAGAGCCGGGGAGCCAGCCTG A G KRBA1 Ensembl:ENSG00000133619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149720806..149720932 26863196 MeRIP-seq:(Medium) rs768677038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955066,Human_RBP_ID_19021596,Human_RBP_ID_22687518 Human_Splice_Rec_935778,Human_Splice_Rec_935779,Human_Splice_Rec_935810,Human_Splice_Rec_935811,Human_Splice_Rec_935840,Human_Splice_Rec_935844,Human_Splice_Rec_935845,Human_Splice_Rec_935870,Human_Splice_Rec_935871,Human_Splice_Rec_935895 71861 RMVar_ID_71861 Human_SNP_ID_344865252 m1A Human chr7 - 149764781 149764781 149764781 CATTCACGGCGAAGCCGCCCACGCGGCCCCGGACGCCGCCCTTGCGGCCCCAGCCTGGTCCGCTC CATTCACGGCGAAGCCGCCCACGCGGCCCCGGCCGCCGCCCTTGCGGCCCCAGCCTGGTCCGCTC T G ZNF467 Ensembl:ENSG00000181444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149764732..149764854 26863196 MeRIP-seq:(Medium) rs886246141 Functional Loss SNV dbSNP153 33..33 33 - - - 71862 RMVar_ID_71862 Human_SNP_ID_344867578 m1A Human chr7 - 149771971 149771971 149771971 TAGGGAAAGGCAGCCTGGAGTCTGAGAGGGGGAGGGGAGCGCTGCCGCCGAGGCGGCCCGGAGCG TAGGGAAAGGCAGCCTGGAGTCTGAGAGGGGGGGGGGAGCGCTGCCGCCGAGGCGGCCCGGAGCG T C ZNF467 Ensembl:ENSG00000181444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr7:149771930..149772038;chr7:149771885..149772014 26863196 MeRIP-seq:(Medium) rs1254990006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267909,Human_RBP_ID_3866907,Human_RBP_ID_8219156,Human_RBP_ID_9439926 71863 RMVar_ID_71863 Human_SNP_ID_344867684 m1A Human chr7 - 149772322 149772322 149772322 GGGGAGGGAAGCGAAGCTGGAGCCTGCTGGGGAGACAGAGGGGGAAGGGAGGCGGGGGCCTCGGA GGGGAGGGAAGCGAAGCTGGAGCCTGCTGGGGGGACAGAGGGGGAAGGGAGGCGGGGGCCTCGGA T C ZNF467 Ensembl:ENSG00000181444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149772320..149772450 26863196 MeRIP-seq:(Medium) rs1343186466 Functional Loss SNV dbSNP153 33..33 33 - - - 71864 RMVar_ID_71864 Human_SNP_ID_344867982 m1A Human chr7 + 149773318 149773318 149773318 TCGAAGCCGGGAAACGGCGCCTGCAAGGGAGGAGGGACCGAGGGAGCGGGCGGAGAGCCCCGGCG TCGAAGCCGGGAAACGGCGCCTGCAAGGGAGGGGGGACCGAGGGAGCGGGCGGAGAGCCCCGGCG A G lnc-SSPO-1 RNACentral:URS00008BD367 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149773267..149773617 26863196 MeRIP-seq:(Medium) rs1197986511 Functional Loss SNV dbSNP153 33..33 33 - - - 71865 RMVar_ID_71865 Human_SNP_ID_344891080 m1A Human chr7 + 149838685 149838685 149838685 GGGGGCCGCCCGCTCCCTCCCGAGGATCCCCGAGCCGGGCTCGGGCGAGGCGGGGCGGCTCGGGC GGGGGCCGCCCGCTCCCTCCCGAGGATCCCCGGGCCGGGCTCGGGCGAGGCGGGGCGGCTCGGGC A G ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149838638..149838747 26863196 MeRIP-seq:(Medium) rs577066832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22621927,Human_RBP_ID_26793705 71866 RMVar_ID_71866 Human_SNP_ID_344891091 m1A Human chr7 + 149838734 149838734 149838734 GCGGGGCGGCTCGGGCGGAGGCCCCGCAGATGAGCCAGGCTTGCAGGGAAGGACTCGCCGGCCCG GCGGGGCGGCTCGGGCGGAGGCCCCGCAGATGGGCCAGGCTTGCAGGGAAGGACTCGCCGGCCCG A G ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:149838506..149838749 26863196 MeRIP-seq:(Medium) rs1021671798 Functional Loss SNV dbSNP153 33..33 33 - - - 71867 RMVar_ID_71867 Human_SNP_ID_344891093 m1A Human chr7 - 149838742 149838742 149838742 AGAGAGGGCGGGCCGGCGAGTCCTTCCCTGCAAGCCTGGCTCATCTGCGGGGCCTCCGCCCGAGC AGAGAGGGCGGGCCGGCGAGTCCTTCCCTGCATGCCTGGCTCATCTGCGGGGCCTCCGCCCGAGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149838442..149838752 26863196 MeRIP-seq:(Medium) rs1259645171 Functional Loss SNV dbSNP153 33..33 33 - - - 71868 RMVar_ID_71868 Human_SNP_ID_344891193 m1A Human chr7 + 149839124 149839124 149839124 CCACTTCTGTTTCTAGGTTATGTACTTCATGGAATATCTGGGCATTGCTTAGAAACCTGTGTCAT CCACTTCTGTTTCTAGGTTATGTACTTCATGGGATATCTGGGCATTGCTTAGAAACCTGTGTCAT A G ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs528471831 Functional Loss SNV dbSNP153 33..33 33 - - - 71869 RMVar_ID_71869 Human_SNP_ID_344892005 m1A Human chr7 + 149842187 149842187 149842187 GGTAGATTCTAAGTTGGTGGGAGGAAGTGTGCAGTCAGGATCTAAAGACTGGGAATGTAGAGAGA GGTAGATTCTAAGTTGGTGGGAGGAAGTGTGCGGTCAGGATCTAAAGACTGGGAATGTAGAGAGA A G ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149842136..149842335 26863196 MeRIP-seq:(Medium) rs1376144987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24199412 71870 RMVar_ID_71870 Human_SNP_ID_344892007 m1A Human chr7 + 149842191 149842191 149842191 GATTCTAAGTTGGTGGGAGGAAGTGTGCAGTCAGGATCTAAAGACTGGGAATGTAGAGAGAGGAA GATTCTAAGTTGGTGGGAGGAAGTGTGCAGTCCGGATCTAAAGACTGGGAATGTAGAGAGAGGAA A C ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149842091..149842299 26863196 MeRIP-seq:(Medium) rs1328444174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24199412 71871 RMVar_ID_71871 Human_SNP_ID_344899171 m1A Human chr7 - 149868400 149868400 149868400 GCCCACTCGGAAAGGCCTGCTGACTGCACTCCAGATGTCAAGAGCACCCTTGGGAAAAAGAAAGG GCCCACTCGGAAAGGCCTGCTGACTGCACTCCGGATGTCAAGAGCACCCTTGGGAAAAAGAAAGG T C ATP6V0E2-AS1 Ensembl:ENSG00000204934 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3735334 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8758 71872 RMVar_ID_71872 Human_SNP_ID_344899172 m1A Human chr7 - 149868400 149868400 149868400 GCCCACTCGGAAAGGCCTGCTGACTGCACTCCAGATGTCAAGAGCACCCTTGGGAAAAAGAAAGG GCCCACTCGGAAAGGCCTGCTGACTGCACTCCCGATGTCAAGAGCACCCTTGGGAAAAAGAAAGG T G ATP6V0E2-AS1 Ensembl:ENSG00000204934 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3735334 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8758 71873 RMVar_ID_71873 Human_SNP_ID_344900424 m1A Human chr7 - 149873367 149873367 149873367 GAAGGCGGGGGCTTCGCGTTTCGATGGCGGGAAGCGGAATGAGGTTGGACCGGCCGGGCCGGCGT GAAGGCGGGGGCTTCGCGTTTCGATGGCGGGAGGCGGAATGAGGTTGGACCGGCCGGGCCGGCGT T C ATP6V0E2-AS1 Ensembl:ENSG00000204934 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:149873266..149873366 26863410 MeRIP-seq:(Medium) rs941281618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4930376 71874 RMVar_ID_71874 Human_SNP_ID_344902110 m1A Human chr7 - 149879323 149879323 149879323 GTCATTCCGAGAGCTGGGCACCTGAAAAGCACATCACATGGAAGGGTCCCGGCCTTGCAGTGGAG GTCATTCCGAGAGCTGGGCACCTGAAAAGCACGTCACATGGAAGGGTCCCGGCCTTGCAGTGGAG T C ATP6V0E2-AS1 Ensembl:ENSG00000204934 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:149879317..149879537 26863410 MeRIP-seq:(Medium) rs549474910 Functional Loss SNV dbSNP153 33..33 33 - - - 71875 RMVar_ID_71875 Human_SNP_ID_344902208 m1A Human chr7 + 149879519 149879509 149879519 CCCAGTCTTCCCAGCCAGCCCGGGCCCTGGGGAGCCCTGGGCACAGCAGCGGCCGAGGGGATGTC CCCAGTCTTCCCAGCCAGCCCGG__________GCCCTGGGCACAGCAGCGGCCGAGGGGATGTC GGCCCTGGGGA G ATP6V0E2 Ensembl:ENSG00000171130 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:149879353..149879653 32194978 MeRIP-seq:(Medium) rs1456009026 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5122934,Human_RBP_ID_17665491,Human_RBP_ID_26550963 71876 RMVar_ID_71876 Human_SNP_ID_557240582 m1A Human chr14 - 60092053 60092053 60092053 GCAGGGAAATAGCGCGCTTCGTTCGCGCCAGGACTAGGCCAACATCTGCCTGGCCGGGGACGACG GCAGGGAAATAGCGCGCTTCGTTCGCGCCAGGGCTAGGCCAACATCTGCCTGGCCGGGGACGACG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:60092001..60092250 26863196 MeRIP-seq:(Medium) rs1160748397 Functional Loss SNV dbSNP153 33..33 33 - - - 71877 RMVar_ID_71877 Human_SNP_ID_557240632 m1A Human chr14 + 60092169 60092169 60092169 CAGACCGGGGCAGCGAGGCCAGCCAGGCGCCGACGAGGTCCCCGAACGCGCACGCGCTCCGTTCA CAGACCGGGGCAGCGAGGCCAGCCAGGCGCCGGCGAGGTCCCCGAACGCGCACGCGCTCCGTTCA A G PCNX4 Ensembl:ENSG00000126773 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:60092001..60092289 26863196 MeRIP-seq:(Medium) rs954830847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4297112 RMVar_hsa_circ_167028,RMVar_hsa_circ_103682 71878 RMVar_ID_71878 Human_SNP_ID_557240662 m1A Human chr14 + 60092223 60092223 60092223 CGCTCCGTTCAGCTCCGGGTGGCGGCCGCCGGAGTAGACGTTAGCCATGGAAACCGAGAGCTGGC CGCTCCGTTCAGCTCCGGGTGGCGGCCGCCGGCGTAGACGTTAGCCATGGAAACCGAGAGCTGGC A C PCNX4 Ensembl:ENSG00000126773 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:60092076..60092350 26863410 MeRIP-seq:(Medium) rs759310235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231178,Human_RBP_ID_4308845 Human_miRNA_ID_3114622 RMVar_hsa_circ_167028,RMVar_hsa_circ_103682 71879 RMVar_ID_71879 Human_SNP_ID_557240663 m1A Human chr14 + 60092223 60092223 60092223 CGCTCCGTTCAGCTCCGGGTGGCGGCCGCCGGAGTAGACGTTAGCCATGGAAACCGAGAGCTGGC CGCTCCGTTCAGCTCCGGGTGGCGGCCGCCGGTGTAGACGTTAGCCATGGAAACCGAGAGCTGGC A T PCNX4 Ensembl:ENSG00000126773 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:60092076..60092350 26863410 MeRIP-seq:(Medium) rs759310235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231178,Human_RBP_ID_4308845 Human_miRNA_ID_3114622 RMVar_hsa_circ_167028,RMVar_hsa_circ_103682 71880 RMVar_ID_71880 Human_SNP_ID_557240721 m1A Human chr14 + 60092348 60092348 60092348 GGGCACTAACCAACCTCCCGGCGGGAGCGCCCAGCCCGAGTTTACCTGCAAAAATGCGGTCCCTG GGGCACTAACCAACCTCCCGGCGGGAGCGCCCCGCCCGAGTTTACCTGCAAAAATGCGGTCCCTG A C PCNX4 Ensembl:ENSG00000126773 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:60092301..60092425 32194978 MeRIP-seq:(Medium) rs1229478378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1521511,Human_Splice_Rec_1521529,Human_Splice_Rec_1521531,Human_Splice_Rec_1521551,Human_Splice_Rec_1521569,Human_Splice_Rec_1521571 Human_miRNA_ID_2005474,Human_miRNA_ID_2579825 RMVar_hsa_circ_167028,RMVar_hsa_circ_103682 71881 RMVar_ID_71881 Human_SNP_ID_557257223 m1A Human chr14 - 60156102 60156102 60156102 TGGTGGTGTGGGTGACTGGAGCCTCGAGTGGAATTGGTGAGGAGCTGGCTTACCAGTTGTCTAAA TGGTGGTGTGGGTGACTGGAGCCTCGAGTGGACTTGGTGAGGAGCTGGCTTACCAGTTGTCTAAA T G DHRS7 Ensembl:ENSG00000100612 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:60156051..60165400 26863196 MeRIP-seq:(Medium) rs200956188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_448997,Human_RBP_ID_4308847,Human_RBP_ID_8406424,Human_RBP_ID_23208717,Human_RBP_ID_23629014 Human_Splice_Rec_1521620,Human_Splice_Rec_1521634,Human_Splice_Rec_1521652,Human_Splice_Rec_1521664,Human_Splice_Rec_1521680,Human_Splice_Rec_1521686,Human_Splice_Rec_1521692,Human_Splice_Rec_1521696 RMVar_hsa_circ_286835,RMVar_hsa_circ_167042,RMVar_hsa_circ_61247,RMVar_hsa_circ_377051 71882 RMVar_ID_71882 Human_SNP_ID_557257245 m1A Human chr14 - 60156151 60156151 60156151 TTTCTTCCTTCCATTTACATTCCTTCCATAGAATGGGAGCTGACTGATATGGTGGTGTGGGTGAC TTTCTTCCTTCCATTTACATTCCTTCCATAGAGTGGGAGCTGACTGATATGGTGGTGTGGGTGAC T C DHRS7 Ensembl:ENSG00000100612 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:60156051..60165400 32194978 MeRIP-seq:(Medium) rs757051755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23629014 Human_Splice_Rec_1521620,Human_Splice_Rec_1521634,Human_Splice_Rec_1521652,Human_Splice_Rec_1521664,Human_Splice_Rec_1521680,Human_Splice_Rec_1521686,Human_Splice_Rec_1521692,Human_Splice_Rec_1521696 RMVar_hsa_circ_286835,RMVar_hsa_circ_167042,RMVar_hsa_circ_61247,RMVar_hsa_circ_377051 71883 RMVar_ID_71883 Human_SNP_ID_557259281 m1A Human chr14 + 60165266 60165266 60165266 GGAAGCGCAGCAGCTGCACCAAGAGCAGGAGCAGCGCGCACAGCACCAGCAGCCACAGCAGCAGC GGAAGCGCAGCAGCTGCACCAAGAGCAGGAGCCGCGCGCACAGCACCAGCAGCCACAGCAGCAGC A C PCNX4 Ensembl:ENSG00000126773 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:60165220..60165347 26863196 MeRIP-seq:(Medium) rs1377722721 Functional Loss SNV dbSNP153 33..33 33 - - - 71884 RMVar_ID_71884 Human_SNP_ID_557280530 m1A Human chr14 - 60249241 60249229 60249241 CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCACCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCC____________GCCGCCTCTAGCGCGGCCCCG CGGCGGCGGCGGT C LOC101927702,LOC101927702:2,LOC101927702:3 RNACentral:URS0000D5AD0A,RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA,lincRNA exon,exon,exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:60249236..60249318 26863410 MeRIP-seq:(Medium) rs1171797597 Functional Loss DEL dbSNP153 33..44 33 - - - 71885 RMVar_ID_71885 Human_SNP_ID_557280535 m1A Human chr14 - 60249241 60249232 60249241 CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCACCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCC_________GCCGCCGCCTCTAGCGCGGCCCCG CGGCGGCGGT C LOC101927702,LOC101927702:2,LOC101927702:3 RNACentral:URS0000D5AD0A,RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA,lincRNA exon,exon,exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:60249236..60249318 26863410 MeRIP-seq:(Medium) rs919070104 Functional Loss DEL dbSNP153 33..41 33 - - - 71886 RMVar_ID_71886 Human_SNP_ID_557280542 m1A Human chr14 - 60249241 60249241 60249241 CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCACCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCGCCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG T C LOC101927702,LOC101927702:2,LOC101927702:3 RNACentral:URS0000D5AD0A,RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA,lincRNA exon,exon,exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:60249236..60249318 26863410 MeRIP-seq:(Medium) rs1486473024 Functional Loss SNV dbSNP153 33..33 33 - - - 71887 RMVar_ID_71887 Human_SNP_ID_557280543 m1A Human chr14 - 60249241 60249241 60249241 CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCACCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG CTCCCGCGCGCGCTCCCGTCCCTAGCGCCGCCCCCGCCGCCGCCGCCGCCTCTAGCGCGGCCCCG T G LOC101927702,LOC101927702:2,LOC101927702:3 RNACentral:URS0000D5AD0A,RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA,lincRNA exon,exon,exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:60249236..60249318 26863410 MeRIP-seq:(Medium) rs1486473024 Functional Loss SNV dbSNP153 33..33 33 - - - 71888 RMVar_ID_71888 Human_SNP_ID_557280549 m1A Human chr14 + 60249255 60249255 60249255 AGGCGGCGGCGGCGGCGGTGGCGGCGCTAGGGACGGGAGCGCGCGCGGGAGCTAGAGAGCAGTGG AGGCGGCGGCGGCGGCGGTGGCGGCGCTAGGGGCGGGAGCGCGCGCGGGAGCTAGAGAGCAGTGG A G PPM1A Ensembl:ENSG00000100614 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:60249208..60249331 26863196 MeRIP-seq:(Medium) rs916926990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4307963 Human_miRNA_ID_1967334 RMVar_hsa_circ_77000,RMVar_hsa_circ_167045 71889 RMVar_ID_71889 Human_SNP_ID_557280688 m1A Human chr14 - 60249578 60249577 60249578 GTCACCGCGGCGGCGACGGCGGCAGCCGGGGGAGGGGTCACCGCTGCAGCGGCGGGCCAGGTCAG GTCACCGCGGCGGCGACGGCGGCAGCCGGGGG_GGGGTCACCGCTGCAGCGGCGGGCCAGGTCAG CT C LOC101927702,LOC101927702:2 RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60249391..60249700 26863196 MeRIP-seq:(Medium) rs1566563628 Functional Loss DEL dbSNP153 33..33 33 - - - 71890 RMVar_ID_71890 Human_SNP_ID_557280689 m1A Human chr14 - 60249578 60249578 60249578 GTCACCGCGGCGGCGACGGCGGCAGCCGGGGGAGGGGTCACCGCTGCAGCGGCGGGCCAGGTCAG GTCACCGCGGCGGCGACGGCGGCAGCCGGGGGGGGGGTCACCGCTGCAGCGGCGGGCCAGGTCAG T C LOC101927702,LOC101927702:2 RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60249391..60249700 26863196 MeRIP-seq:(Medium) rs893776387 Functional Loss SNV dbSNP153 33..33 33 - - - 71891 RMVar_ID_71891 Human_SNP_ID_557280691 m1A Human chr14 - 60249615 60249579 60249615 GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGGAGGGGGTCACCGCGGCGGCGACGGCGGCAGCCG GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGG_________________________________ CCCCCGGCTGCCGCCGTCGCCGCCGCGGTGACCCCCT C LOC101927702,LOC101927702:2 RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr14:60249371..60249717;chr14:60249521..60249667 26863196 MeRIP-seq:(Medium) rs766737372 Functional Loss DEL dbSNP153 33..65 33 - - - 71892 RMVar_ID_71892 Human_SNP_ID_557280695 m1A Human chr14 - 60249615 60249580 60249615 GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGGAGGGGGTCACCGCGGCGGCGACGGCGGCAGCCG GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGG_________________________________ CCCCGGCTGCCGCCGTCGCCGCCGCGGTGACCCCCT C LOC101927702,LOC101927702:2 RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr14:60249371..60249717;chr14:60249521..60249667 26863196 MeRIP-seq:(Medium) rs1386166155 Functional Loss DEL dbSNP153 33..65 33 - - - 71893 RMVar_ID_71893 Human_SNP_ID_557280707 m1A Human chr14 - 60249615 60249615 60249615 GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGGAGGGGGTCACCGCGGCGGCGACGGCGGCAGCCG GTCGGCCGAGGCGGCGGCGGCGGCAGCCGGGGGGGGGGTCACCGCGGCGGCGACGGCGGCAGCCG T C LOC101927702,LOC101927702:2 RNACentral:URS0000D593C1,RNACentral:URS0000D58C33 lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr14:60249371..60249717;chr14:60249521..60249667 26863196 MeRIP-seq:(Medium) rs1023653808 Functional Loss SNV dbSNP153 33..33 33 - - - 71894 RMVar_ID_71894 Human_SNP_ID_557288709 m1A Human chr14 + 60282643 60282643 60282643 ATTAAAAAGATTGTTTGGTACATATTTTGTTTATAAGACAGTTATTGACTTTCCTGTTTCTCTTC ATTAAAAAGATTGTTTGGTACATATTTTGTTTCTAAGACAGTTATTGACTTTCCTGTTTCTCTTC A C PPM1A Ensembl:ENSG00000100614 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60282640..60282805 26863196 MeRIP-seq:(Medium) rs764468215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2419029,Human_RBP_ID_12370986,Human_RBP_ID_22539987,Human_RBP_ID_22737356 RMVar_hsa_circ_77000,RMVar_hsa_circ_167045 71895 RMVar_ID_71895 Human_SNP_ID_557288710 m1A Human chr14 + 60282645 60282645 60282645 TAAAAAGATTGTTTGGTACATATTTTGTTTATAAGACAGTTATTGACTTTCCTGTTTCTCTTCCT TAAAAAGATTGTTTGGTACATATTTTGTTTATGAGACAGTTATTGACTTTCCTGTTTCTCTTCCT A G PPM1A Ensembl:ENSG00000100614 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:60282643..60282841 26863196 MeRIP-seq:(Medium) rs922216752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2419029,Human_RBP_ID_12370986,Human_RBP_ID_22539987,Human_RBP_ID_22737356 RMVar_hsa_circ_77000,RMVar_hsa_circ_167045 71896 RMVar_ID_71896 Human_SNP_ID_557288765 m1A Human chr14 - 60282852 60282852 60282852 CATCATACACAGCAAAGAATGACCACGATTCAAGTCCACTTGGCAAACCGATCACAGCCGTATGT CATCATACACAGCAAAGAATGACCACGATTCAGGTCCACTTGGCAAACCGATCACAGCCGTATGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:60282801..60282900 32194978 MeRIP-seq:(Medium) rs1463007357 Functional Loss SNV dbSNP153 33..33 33 - - - 71897 RMVar_ID_71897 Human_SNP_ID_557290498 m1A Human chr14 + 60289877 60289877 60289877 TCCATGTGATGCGCACATTAGCGAGTGAGAACATCCCCAGCCTCCCACCAGGGGGTGAATTGGCA TCCATGTGATGCGCACATTAGCGAGTGAGAACGTCCCCAGCCTCCCACCAGGGGGTGAATTGGCA A G PPM1A Ensembl:ENSG00000100614 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:60289826..60289925 32194978 MeRIP-seq:(Medium) rs1375464368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1496303,Human_RBP_ID_1821512,Human_RBP_ID_12371100,Human_RBP_ID_17856437,Human_RBP_ID_23629155 Human_Splice_Rec_1521712,Human_Splice_Rec_1521713,Human_Splice_Rec_1521724,Human_Splice_Rec_1521725,Human_Splice_Rec_1521732,Human_Splice_Rec_1521733,Human_Splice_Rec_1521742,Human_Splice_Rec_1521743 Human_miRNA_ID_2685129,Human_miRNA_ID_2715184,Human_miRNA_ID_3051166 RMVar_hsa_circ_77000,RMVar_hsa_circ_83521,RMVar_hsa_circ_167045,RMVar_hsa_circ_314634,RMVar_hsa_circ_167050,RMVar_hsa_circ_167051 71898 RMVar_ID_71898 Human_SNP_ID_557315508 m1A Human chr14 + 60398115 60398115 60398115 AACAGGATATCTGAAGGGGTATACTCTAGTTGAATATGAAACATACAAGGAAGCCCAGGCTGCTA AACAGGATATCTGAAGGGGTATACTCTAGTTGCATATGAAACATACAAGGAAGCCCAGGCTGCTA A C RBM8B Ensembl:ENSG00000258427 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1470914645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449231,Human_RBP_ID_1821544,Human_RBP_ID_6402953,Human_RBP_ID_17481244,Human_RBP_ID_18653101 71899 RMVar_ID_71899 Human_SNP_ID_557376256 m1A Human chr14 - 60649125 60649125 60649125 GGAGCAAGTGGCGTGCGTGTGCGAGGTTCTGCAGCAAGGCGGAAACCTGGAGCGCCTGGGCAGGT GGAGCAAGTGGCGTGCGTGTGCGAGGTTCTGCTGCAAGGCGGAAACCTGGAGCGCCTGGGCAGGT T A SIX1 Ensembl:ENSG00000126778 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:60649076..60649175 32194978 MeRIP-seq:(Medium) rs1177617020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6365720,Human_RBP_ID_27432001 71900 RMVar_ID_71900 Human_SNP_ID_557376353 m1A Human chr14 - 60649302 60649302 60649302 TTCCGACTCCGGTTTTCGCCTTTGCAAAGCCTAAGGAGGAGGTTAGGAACAGCCGCGCCCCCCTC TTCCGACTCCGGTTTTCGCCTTTGCAAAGCCTGAGGAGGAGGTTAGGAACAGCCGCGCCCCCCTC T C SIX1 Ensembl:ENSG00000126778 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:60649251..60649452 32194978 MeRIP-seq:(Medium) rs1266976548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4313420 71901 RMVar_ID_71901 Human_SNP_ID_557376381 m1A Human chr14 + 60649374 60649374 60649374 GTGGGCGGCCAAGGAAGAGAAGGCGGAGGAGTAGGGGAGGTTCTGGACACGGAACGGCCGGCGCA GTGGGCGGCCAAGGAAGAGAAGGCGGAGGAGTCGGGGAGGTTCTGGACACGGAACGGCCGGCGCA A C SALRNA1 RNACentral:URS00008B9496 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr14:60649323..60649440;chr14:60649281..60649408 26863196 MeRIP-seq:(Medium) rs745791461 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_300 71902 RMVar_ID_71902 Human_SNP_ID_557376382 m1A Human chr14 + 60649374 60649374 60649374 GTGGGCGGCCAAGGAAGAGAAGGCGGAGGAGTAGGGGAGGTTCTGGACACGGAACGGCCGGCGCA GTGGGCGGCCAAGGAAGAGAAGGCGGAGGAGTGGGGGAGGTTCTGGACACGGAACGGCCGGCGCA A G SALRNA1 RNACentral:URS00008B9496 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr14:60649323..60649440;chr14:60649281..60649408 26863196 MeRIP-seq:(Medium) rs745791461 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_300 71903 RMVar_ID_71903 Human_SNP_ID_557395737 m1A Human chr14 - 60724301 60724301 60724301 ACCGGAGGAGTCACGTTGGGGGAACGGCAGAAAGCAGCTATCCGTTTACACTACTTTGCTCTAAC ACCGGAGGAGTCACGTTGGGGGAACGGCAGAATGCAGCTATCCGTTTACACTACTTTGCTCTAAC T A SIX4 Ensembl:ENSG00000100625 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60724074..60724301 26863196 MeRIP-seq:(Medium) rs1391081417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1521883 71904 RMVar_ID_71904 Human_SNP_ID_557395738 m1A Human chr14 - 60724301 60724301 60724301 ACCGGAGGAGTCACGTTGGGGGAACGGCAGAAAGCAGCTATCCGTTTACACTACTTTGCTCTAAC ACCGGAGGAGTCACGTTGGGGGAACGGCAGAAGGCAGCTATCCGTTTACACTACTTTGCTCTAAC T C SIX4 Ensembl:ENSG00000100625 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60724074..60724301 26863196 MeRIP-seq:(Medium) rs1391081417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1521883 71905 RMVar_ID_71905 Human_SNP_ID_557398192 m1A Human chr14 + 60734856 60734843 60734857 AAACAGGCGCCTGCGAGAGTCTGTAGGAGGGAAACCGCCATGGACGATCAGGGTTGCCCTCGGTG AAACAGGCGCCTGCGAGAGT______________CCGCCATGGACGATCAGGGTTGCCCTCGGTG TCTGTAGGAGGGAAA T MNAT1 Ensembl:ENSG00000020426 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:60734811..60734900 26863196 MeRIP-seq:(Medium) rs1187837051 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_1496436,Human_RBP_ID_4308364,Human_RBP_ID_5463793,Human_RBP_ID_8795302,Human_RBP_ID_18653168,Human_RBP_ID_23118312,Human_RBP_ID_23629407,Human_RBP_ID_27808909 Human_Splice_Rec_1521887,Human_Splice_Rec_1521889,Human_Splice_Rec_1521903,Human_Splice_Rec_1521909,Human_Splice_Rec_1521921 71906 RMVar_ID_71906 Human_SNP_ID_557407786 m1A Human chr14 - 60776273 60776273 60776273 AACACCTTTCCCTCTCCTTTCAGATGACTTGCATTAAATACCACTACTCTATCCTTTGACCTCAC AACACCTTTCCCTCTCCTTTCAGATGACTTGCTTTAAATACCACTACTCTATCCTTTGACCTCAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:60776264..60776377 26863196 MeRIP-seq:(Medium) rs1044113519 Functional Loss SNV dbSNP153 33..33 33 - - - 71907 RMVar_ID_71907 Human_SNP_ID_557453861 m1A Human chr14 + 60968312 60968312 60968312 TACTTCTTCTCTTGCTTGTCACAGAGCACTACAGGATGCATTCAGTGGGCTTTTCTGGCAGCCCA TACTTCTTCTCTTGCTTGTCACAGAGCACTACGGGATGCATTCAGTGGGCTTTTCTGGCAGCCCA A G AL160236.2,MNAT1 Ensembl:ENSG00000258892,Ensembl:ENSG00000020426 lincRNA,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:60968268..60968368 32194978 MeRIP-seq:(Medium) rs1254375954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449345,Human_RBP_ID_25124188 Human_Splice_Rec_1521902,Human_Splice_Rec_1521920,Human_Splice_Rec_1521948,Human_Splice_Rec_1521949 71908 RMVar_ID_71908 Human_SNP_ID_557454733 m1A Human chr14 - 60972451 60972451 60972451 CCGCCGCCGCCGCCGCCATGCCCAAGAGAAAGACTGAAGGGGATGCTAAAGGAGATAAAGCCAAG CCGCCGCCGCCGCCGCCATGCCCAAGAGAAAGGCTGAAGGGGATGCTAAAGGAGATAAAGCCAAG T C TRMT5,AL160236.1 Ensembl:ENSG00000126814,Ensembl:ENSG00000258656 Protein coding,Pseudogene 3'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:60972299..60972559 26863196 MeRIP-seq:(Medium) rs1345095453 Functional Loss SNV dbSNP153 33..33 33 - - - 71909 RMVar_ID_71909 Human_SNP_ID_557454776 m1A Human chr14 + 60972496 60972496 60972496 CATGGCGGCGGCGGCGGCGGCGGGATGTGGGCACCGGGTGTGGGACGCAGCAGCGCGCGGGCTTT CATGGCGGCGGCGGCGGCGGCGGGATGTGGGCCCCGGGTGTGGGACGCAGCAGCGCGCGGGCTTT A C AL160236.2 Ensembl:ENSG00000258892 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:60972446..60972549;chr14:60972449..60972577 26863196 MeRIP-seq:(Medium) rs1215273175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26778427 71910 RMVar_ID_71910 Human_SNP_ID_557456930 m1A Human chr14 - 60981025 60981025 60981025 CGCGACCCACATCCGATCGGTACCGGAGCGGGAGGTGAGGGGTCGGCTCGCGGATCCAGCTGCAG CGCGACCCACATCCGATCGGTACCGGAGCGGGCGGTGAGGGGTCGGCTCGCGGATCCAGCTGCAG T G TRMT5 Ensembl:ENSG00000126814 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:60980858..60981058;chr14:60980900..60981028 26863196 MeRIP-seq:(Medium) rs1390053940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308366,Human_RBP_ID_5418210,Human_RBP_ID_5493731 Human_Splice_Rec_1521953,Human_Splice_Rec_1521961 71911 RMVar_ID_71911 Human_SNP_ID_557457053 m1A Human chr14 + 60981254 60981254 60981254 GCGCAGGGCAGGGGTAGAGGCTCGTAGATGGAACTGGTAGTCAGCTGGAGAGCAGCATGGAGGCG GCGCAGGGCAGGGGTAGAGGCTCGTAGATGGAGCTGGTAGTCAGCTGGAGAGCAGCATGGAGGCG A G AL160236.2,SLC38A6 Ensembl:ENSG00000258892,Ensembl:ENSG00000139974 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:60981204..60981317 26863196 MeRIP-seq:(Medium) rs750342980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449365,Human_RBP_ID_882400,Human_RBP_ID_1275689,Human_RBP_ID_1502549,Human_RBP_ID_4297489,Human_RBP_ID_5564745,Human_RBP_ID_24367751 RMVar_hsa_circ_104403,RMVar_hsa_circ_167072 71912 RMVar_ID_71912 Human_SNP_ID_557457055 m1A Human chr14 - 60981262 60981259 60981263 CCCCAGGACGCCTCCATGCTGCTCTCCAGCTGACTACCAGTTCCATCTACGAGCCTCTACCCCTG CCCCAGGACGCCTCCATGCTGCTCTCCAGCT____ACCAGTTCCATCTACGAGCCTCTACCCCTG TAGTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:60981157..60981364 26863196 MeRIP-seq:(Medium) rs747624776 Functional Loss DEL dbSNP153 32..35 33 - - - 71913 RMVar_ID_71913 Human_SNP_ID_557457101 m1A Human chr14 + 60981351 60981351 60981351 GTATGTCTCTGTCCAGCAGCCTGAAGAAGCGGAGGCCGAAGAGTTGAGTCCGTTGCTAAGCAACG GTATGTCTCTGTCCAGCAGCCTGAAGAAGCGGGGGCCGAAGAGTTGAGTCCGTTGCTAAGCAACG A G AL160236.2,SLC38A6 Ensembl:ENSG00000258892,Ensembl:ENSG00000139974 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:60981186..60981662 26863196 MeRIP-seq:(Medium) rs1328299739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5564745,Human_RBP_ID_18980672 Human_Splice_Rec_1521965,Human_Splice_Rec_1521997,Human_Splice_Rec_1522065,Human_Splice_Rec_1522071,Human_Splice_Rec_1522077,Human_Splice_Rec_1522117 RMVar_hsa_circ_104403,RMVar_hsa_circ_167072 71914 RMVar_ID_71914 Human_SNP_ID_557542400 m1A Human chr14 + 61321749 61321749 61321749 GGGAAGAGACGCTTGGGGCTGGGGCTCACCGGACGGGTAGGTCCGGCTCTCCAGGGAGAGGAGCT GGGAAGAGACGCTTGGGGCTGGGGCTCACCGGTCGGGTAGGTCCGGCTCTCCAGGGAGAGGAGCT A T PRKCH Ensembl:ENSG00000027075 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:61321578..61321988 26863196 MeRIP-seq:(Medium) rs944429450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78511,RMVar_hsa_circ_167086 71915 RMVar_ID_71915 Human_SNP_ID_557566299 m1A Human chr14 - 61421954 61421954 61421954 TCCCTGTCTAGCCTGGGGTCCACACCTGCCCTAATCTCTTTCTTCCTCTCCTCTCCTAACTCTCC TCCCTGTCTAGCCTGGGGTCCACACCTGCCCTGATCTCTTTCTTCCTCTCCTCTCCTAACTCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:61421907..61422003 26863196 MeRIP-seq:(Medium) rs546337570 Functional Loss SNV dbSNP153 33..33 33 - - - 71916 RMVar_ID_71916 Human_SNP_ID_557566300 m1A Human chr14 - 61421954 61421954 61421954 TCCCTGTCTAGCCTGGGGTCCACACCTGCCCTAATCTCTTTCTTCCTCTCCTCTCCTAACTCTCC TCCCTGTCTAGCCTGGGGTCCACACCTGCCCTCATCTCTTTCTTCCTCTCCTCTCCTAACTCTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:61421907..61422003 26863196 MeRIP-seq:(Medium) rs546337570 Functional Loss SNV dbSNP153 33..33 33 - - - 71917 RMVar_ID_71917 Human_SNP_ID_557597431 m1A Human chr14 - 61547817 61547817 61547817 TTCAGCTGGGCCCAGTCGATTTCCTTAAAAAAAGGATGTCTCAAGATGGCGTGCTCGCCTCCCTG TTCAGCTGGGCCCAGTCGATTTCCTTAAAAAAGGGATGTCTCAAGATGGCGTGCTCGCCTCCCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:61530515..61547857 32194978 MeRIP-seq:(Medium) rs1476895904 Functional Loss SNV dbSNP153 33..33 33 - - - 71918 RMVar_ID_71918 Human_SNP_ID_557642736 m1A Human chr14 + 61740860 61740860 61740860 ATCAGTTGTCACCATTAGAAAGCAGTTCCGCAAGCCCTGAAAGCGCAAGTCCTCAAAGCACAGTT ATCAGTTGTCACCATTAGAAAGCAGTTCCGCAGGCCCTGAAAGCGCAAGTCCTCAAAGCACAGTT A G HIF1A,AL137129.1 Ensembl:ENSG00000100644,Ensembl:ENSG00000258964 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:61740810..61740948 26863196 MeRIP-seq:(Medium) rs1042346794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3469733,Human_RBP_ID_8406818,Human_RBP_ID_8795366,Human_RBP_ID_17248924 Human_miRNA_ID_2353862,Human_miRNA_ID_2353863 RMVar_hsa_circ_167096,RMVar_hsa_circ_12679,RMVar_hsa_circ_113772,RMVar_hsa_circ_167095,RMVar_hsa_circ_337622,RMVar_hsa_circ_167106,RMVar_hsa_circ_167105,RMVar_hsa_circ_307437,RMVar_hsa_circ_321072,RMVar_hsa_circ_7594,RMVar_hsa_circ_13717,RMVar_hsa_circ_167108,RMVar_hsa_circ_167107,RMVar_hsa_circ_331567,RMVar_hsa_circ_278911,RMVar_hsa_circ_43837,RMVar_hsa_circ_167114,RMVar_hsa_circ_108880,RMVar_hsa_circ_56077,RMVar_hsa_circ_167120,RMVar_hsa_circ_167124,RMVar_hsa_circ_280104,RMVar_hsa_circ_307590,RMVar_hsa_circ_167123,RMVar_hsa_circ_167126,RMVar_hsa_circ_306207,RMVar_hsa_circ_317068,RMVar_hsa_circ_277948,RMVar_hsa_circ_167125 71919 RMVar_ID_71919 Human_SNP_ID_557645411 m1A Human chr14 - 61751076 61751076 61751076 TCGCATCCTCATCATGTAGCGCCAGCCACACCAGGAACAGAAGGGTGCCGGGTACCTTCCGCATG TCGCATCCTCATCATGTAGCGCCAGCCACACCCGGAACAGAAGGGTGCCGGGTACCTTCCGCATG T G HIF1A-AS3 Ensembl:ENSG00000258667 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:61751026..61751075 32194978 MeRIP-seq:(Medium) rs73317115 Functional Loss SNV dbSNP153 33..33 33 - - - 71920 RMVar_ID_71920 Human_SNP_ID_557648575 m1A Human chr14 - 61762472 61762472 61762472 AGCAGCGCCTCGCAGTCGGTCTGCAGGCCGGGAGGAGTCCCCATGGCACCCGAAGCCCGCACGCC AGCAGCGCCTCGCAGTCGGTCTGCAGGCCGGGGGGAGTCCCCATGGCACCCGAAGCCCGCACGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:61762423..61762540;chr14:61762421..61762526 26863196 MeRIP-seq:(Medium) rs970184322 Functional Loss SNV dbSNP153 33..33 33 - - - 71921 RMVar_ID_71921 Human_SNP_ID_557648583 m1A Human chr14 - 61762480 61762480 61762480 AGCGGCTGAGCAGCGCCTCGCAGTCGGTCTGCAGGCCGGGAGGAGTCCCCATGGCACCCGAAGCC AGCGGCTGAGCAGCGCCTCGCAGTCGGTCTGCCGGCCGGGAGGAGTCCCCATGGCACCCGAAGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:61762430..61762550 26863196 MeRIP-seq:(Medium) rs774629397 Functional Loss SNV dbSNP153 33..33 33 - - - 71922 RMVar_ID_71922 Human_SNP_ID_557648594 m1A Human chr14 - 61762501 61762501 61762501 GTACACTGTCCGTCTCCTGGAAGCGGCTGAGCAGCGCCTCGCAGTCGGTCTGCAGGCCGGGAGGA GTACACTGTCCGTCTCCTGGAAGCGGCTGAGCTGCGCCTCGCAGTCGGTCTGCAGGCCGGGAGGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:61762405..61762554 26863410 MeRIP-seq:(Medium) rs1174255290 Functional Loss SNV dbSNP153 33..33 33 - - - 71923 RMVar_ID_71923 Human_SNP_ID_557648665 m1A Human chr14 + 61762606 61762606 61762606 CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCACCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCCCCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA A C SNAPC1,AL137129.1 Ensembl:ENSG00000023608,Ensembl:ENSG00000258964 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:61762601..61762650 32194978 MeRIP-seq:(Medium) rs773086688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19064091,Human_RBP_ID_27808918 71924 RMVar_ID_71924 Human_SNP_ID_557648666 m1A Human chr14 + 61762606 61762606 61762606 CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCACCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCGCCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA A G SNAPC1,AL137129.1 Ensembl:ENSG00000023608,Ensembl:ENSG00000258964 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:61762601..61762650 32194978 MeRIP-seq:(Medium) rs773086688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19064091,Human_RBP_ID_27808918 71925 RMVar_ID_71925 Human_SNP_ID_557651361 m1A Human chr14 - 61771656 61771656 61771656 TATATACAACCATTCCCTCTAACTAGCTCCTTACCTCAACTCCAAACATAAACATTATGTCTCTC TATATACAACCATTCCCTCTAACTAGCTCCTTTCCTCAACTCCAAACATAAACATTATGTCTCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:61771542..61771721 26863196 MeRIP-seq:(Medium) rs1050552987 Functional Loss SNV dbSNP153 33..33 33 - - - 71926 RMVar_ID_71926 Human_SNP_ID_557652752 m1A Human chr14 + 61776201 61776201 61776201 AGCCCTCAGCTTGATAAAGGATGATTTTTTTGACAATATTAAGAACATAGTTTTGGAGCATCAGC AGCCCTCAGCTTGATAAAGGATGATTTTTTTGGCAATATTAAGAACATAGTTTTGGAGCATCAGC A G SNAPC1,AL137129.1 Ensembl:ENSG00000023608,Ensembl:ENSG00000258964 Protein coding,lincRNA CDS,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:61776151..61776225 32194978 MeRIP-seq:(Medium) rs1470787609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095564,Human_RBP_ID_5564780,Human_RBP_ID_12377343 Human_Splice_Rec_1522795 RMVar_hsa_circ_167129,RMVar_hsa_circ_167128,RMVar_hsa_circ_337720,RMVar_hsa_circ_314015,RMVar_hsa_circ_90192,RMVar_hsa_circ_313123,RMVar_hsa_circ_332761 71927 RMVar_ID_71927 Human_SNP_ID_558086319 m1A Human chr14 - 63508176 63508176 63508176 GGTGTGTGAGGTGTGCGAGGAGGGAAGAGCACACACTTGGTAATGAAGGCCTGAGAGCTGCAGGG GGTGTGTGAGGTGTGCGAGGAGGGAAGAGCACGCACTTGGTAATGAAGGCCTGAGAGCTGCAGGG T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:63508174..63508326 26863196 MeRIP-seq:(Medium) rs375788974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23630468 Human_Splice_Rec_1523027,Human_Splice_Rec_1523077 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 71928 RMVar_ID_71928 Human_SNP_ID_558095534 m1A Human chr14 + 63542876 63542876 63542876 TGGCCGCAGCGGGGGCGGGCGGCGGGACCGGGACGTGCAGGGGGAGGTCCGGGCAGCTGCGGGGA TGGCCGCAGCGGGGGCGGGCGGCGGGACCGGGTCGTGCAGGGGGAGGTCCGGGCAGCTGCGGGGA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:63539688..63542875 26863196 MeRIP-seq:(Medium) rs1222801960 Functional Loss SNV dbSNP153 33..33 33 - - - 71929 RMVar_ID_71929 Human_SNP_ID_558122386 m1A Human chr14 - 63642140 63642140 63642140 CAGTCAGCCACGAGGAAGGCGGAATCCGCCTTATTCTTGCCCTTTATTGGCCACGCATCCCACCA CAGTCAGCCACGAGGAAGGCGGAATCCGCCTTGTTCTTGCCCTTTATTGGCCACGCATCCCACCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:63642109..63642194 26863196 MeRIP-seq:(Medium) rs1215517041 Functional Loss SNV dbSNP153 33..33 33 - - - 71930 RMVar_ID_71930 Human_SNP_ID_558122398 m1A Human chr14 - 63642156 63642156 63642156 TACCAGCGGATGCATCCAGTCAGCCACGAGGAAGGCGGAATCCGCCTTATTCTTGCCCTTTATTG TACCAGCGGATGCATCCAGTCAGCCACGAGGACGGCGGAATCCGCCTTATTCTTGCCCTTTATTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:63642113..63642233 26863196 MeRIP-seq:(Medium) rs370866182 Functional Loss SNV dbSNP153 33..33 33 - - - 71931 RMVar_ID_71931 Human_SNP_ID_558143896 m1A Human chr14 - 63727856 63727856 63727856 AGTGGCCCGTTTCCAGCGGCTGTGCGGGGTGGAAGCGCCGCCGCGCCGCTCAGCAGACCGGAGGG AGTGGCCCGTTTCCAGCGGCTGTGCGGGGTGGTAGCGCCGCCGCGCCGCTCAGCAGACCGGAGGG T A SGPP1 Ensembl:ENSG00000126821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:63727741..63727990 32194978 MeRIP-seq:(Medium) rs765677196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4307966 71932 RMVar_ID_71932 Human_SNP_ID_558175478 m1A Human chr14 + 63853071 63853046 63853071 GCGAGAGGGAGAGCGAGCAAAAGGCGCGATCCAGAGAGCCAGGCAAGCGGGGCGCCGACCTCGGG GCGAGAGG_________________________GAGAGCCAGGCAAGCGGGGCGCCGACCTCGGG GGAGAGCGAGCAAAAGGCGCGATCCA G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:63853027..63853179 26863196 MeRIP-seq:(Medium) rs1207682752 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_4313548 Human_Splice_Rec_1523217,Human_Splice_Rec_1523447,Human_Splice_Rec_1523675,Human_Splice_Rec_1523903 71933 RMVar_ID_71933 Human_SNP_ID_558175490 m1A Human chr14 + 63853075 63853075 63853075 GAGGGAGAGCGAGCAAAAGGCGCGATCCAGAGAGCCAGGCAAGCGGGGCGCCGACCTCGGGCGGC GAGGGAGAGCGAGCAAAAGGCGCGATCCAGAGGGCCAGGCAAGCGGGGCGCCGACCTCGGGCGGC A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:63853025..63853876 26863196 MeRIP-seq:(Medium) rs1473279305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1523217,Human_Splice_Rec_1523447,Human_Splice_Rec_1523675,Human_Splice_Rec_1523903 71934 RMVar_ID_71934 Human_SNP_ID_558175707 m1A Human chr14 - 63853656 63853656 63853656 GCGGGTTCCCGGGTCCCCGGGGCGAGCACCGCACCGCTCACGATCCTGCAATCTCTGCGCCGCGG GCGGGTTCCCGGGTCCCCGGGGCGAGCACCGCCCCGCTCACGATCCTGCAATCTCTGCGCCGCGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:63853632..63853769 26863196 MeRIP-seq:(Medium) rs1168687902 Functional Loss SNV dbSNP153 33..33 33 - - - 71935 RMVar_ID_71935 Human_SNP_ID_558214204 m1A Human chr14 - 64005026 64005026 64005026 GACCCTTGTACCTACTGCTGCCTCTGCCTAGAAGGCTATTTCTCCAGGTTCAAGTGGCTTGCTCT GACCCTTGTACCTACTGCTGCCTCTGCCTAGATGGCTATTTCTCCAGGTTCAAGTGGCTTGCTCT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:64004983..64005115 26863196 MeRIP-seq:(Medium) rs117951391 Functional Loss SNV dbSNP153 33..33 33 - - - 71936 RMVar_ID_71936 Human_SNP_ID_558268902 m1A Human chr14 + 64210026 64210026 64210026 AGCAGTACCGGCGGCTGGCCCGGGAGAACCGCACAGACACGGCCAGCAGGCTGAAGCAGATGGTC AGCAGTACCGGCGGCTGGCCCGGGAGAACCGCGCAGACACGGCCAGCAGGCTGAAGCAGATGGTC A G SYNE2 Ensembl:ENSG00000054654 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64209976..64210050 32194978 MeRIP-seq:(Medium) rs766341717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1523420,Human_Splice_Rec_1523421,Human_Splice_Rec_1523652,Human_Splice_Rec_1523653,Human_Splice_Rec_1523878,Human_Splice_Rec_1523879,Human_Splice_Rec_1524238,Human_Splice_Rec_1524239,Human_Splice_Rec_1524396,Human_Splice_Rec_1524397,Human_Splice_Rec_1524542,Human_Splice_Rec_1524543,Human_Splice_Rec_1524660,Human_Splice_Rec_1524661,Human_Splice_Rec_1524716,Human_Splice_Rec_1524717,Human_Splice_Rec_1524760,Human_Splice_Rec_1524761,Human_Splice_Rec_1524786,Human_Splice_Rec_1524787,Human_Splice_Rec_1524811 Human_miRNA_ID_1093111,Human_miRNA_ID_2077135,Human_miRNA_ID_2141416,Human_miRNA_ID_2512453,Human_miRNA_ID_3055275 RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_269534,RMVar_hsa_circ_300508,RMVar_hsa_circ_100865,RMVar_hsa_circ_167235,RMVar_hsa_circ_266659,RMVar_hsa_circ_328233,RMVar_hsa_circ_320795,RMVar_hsa_circ_167237,RMVar_hsa_circ_36079,RMVar_hsa_circ_118165,RMVar_hsa_circ_167238,RMVar_hsa_circ_167239 71937 RMVar_ID_71937 Human_SNP_ID_558269452 m1A Human chr14 + 64211934 64211934 64211934 TCTGTCTGAACTCTTGTTCCGTGGTCAGTAGAAATGTGATTTCCTCCCCACTTTTGCAGCATTTC TCTGTCTGAACTCTTGTTCCGTGGTCAGTAGAGATGTGATTTCCTCCCCACTTTTGCAGCATTTC A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64211931..64212043 26863196 MeRIP-seq:(Medium) rs1420924507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_269534,RMVar_hsa_circ_300508,RMVar_hsa_circ_100865,RMVar_hsa_circ_167235,RMVar_hsa_circ_266659,RMVar_hsa_circ_36079,RMVar_hsa_circ_118165,RMVar_hsa_circ_167238,RMVar_hsa_circ_167239 71938 RMVar_ID_71938 Human_SNP_ID_558270041 m1A Human chr14 + 64214234 64214234 64214234 AGATGAAAAGGAGGCCTCTGAGAATGAAACAGACATGGAAGACCCCAGAGAAATCCAGACTGATT AGATGAAAAGGAGGCCTCTGAGAATGAAACAGCCATGGAAGACCCCAGAGAAATCCAGACTGATT A C SYNE2 Ensembl:ENSG00000054654 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64214226..64214250 32194978 MeRIP-seq:(Medium) rs776820284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1822124,Human_RBP_ID_18653692 Human_Splice_Rec_1523426,Human_Splice_Rec_1523658,Human_Splice_Rec_1523884,Human_Splice_Rec_1524244,Human_Splice_Rec_1524402,Human_Splice_Rec_1524548,Human_Splice_Rec_1524666,Human_Splice_Rec_1524722,Human_Splice_Rec_1524766,Human_Splice_Rec_1524792,Human_Splice_Rec_1524816 Human_miRNA_ID_954728,Human_miRNA_ID_1546396,Human_miRNA_ID_2157767,Human_miRNA_ID_2424806,Human_miRNA_ID_2434468 RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_300508,RMVar_hsa_circ_100865,RMVar_hsa_circ_167235,RMVar_hsa_circ_266659,RMVar_hsa_circ_36079,RMVar_hsa_circ_118165,RMVar_hsa_circ_167238,RMVar_hsa_circ_167239 71939 RMVar_ID_71939 Human_SNP_ID_558303478 m1A Human chr14 + 64338557 64338557 64338557 TGCCTGGAAGCCGGGCGCCCTCACACTTCTGCACCGCGTCCCCAGAGCTGAGGAGCATCCGGGAG TGCCTGGAAGCCGGGCGCCCTCACACTTCTGCCCCGCGTCCCCAGAGCTGAGGAGCATCCGGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64338402..64338599 26863196 MeRIP-seq:(Medium) rs897175942 Functional Loss SNV dbSNP153 33..33 33 - - - 71940 RMVar_ID_71940 Human_SNP_ID_558318894 m1A Human chr14 - 64400743 64400743 64400743 GGTGGGGTTAACACTGAATGTTTCAAGCACAAATAAGTGATGCAGATTATTAGATGTATTTCTCT GGTGGGGTTAACACTGAATGTTTCAAGCACAAGTAAGTGATGCAGATTATTAGATGTATTTCTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64400741..64400850 26863196 MeRIP-seq:(Medium) rs200115519 Functional Loss SNV dbSNP153 33..33 33 - - - 71941 RMVar_ID_71941 Human_SNP_ID_558321308 m1A Human chr14 + 64411136 64411136 64411136 TGATTCCAATCTTTATATAAATGTGAAGCTGAAGGCTGCTGAAGAGGTAACGCCAGAAGAGCTGT TGATTCCAATCTTTATATAAATGTGAAGCTGAGGGCTGCTGAAGAGGTAACGCCAGAAGAGCTGT A G MTHFD1 Ensembl:ENSG00000100714 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64400776..64415461 32194978 MeRIP-seq:(Medium) rs201428609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880548,Human_RBP_ID_3944959,Human_RBP_ID_17856443 Human_Splice_Rec_1525130,Human_Splice_Rec_1525131,Human_Splice_Rec_1525186,Human_Splice_Rec_1525187,Human_Splice_Rec_1525196,Human_Splice_Rec_1525197,Human_Splice_Rec_1525250,Human_Splice_Rec_1525251,Human_Splice_Rec_1525316,Human_Splice_Rec_1525317,Human_Splice_Rec_1525372,Human_Splice_Rec_1525373,Human_Splice_Rec_1525424,Human_Splice_Rec_1525425,Human_Splice_Rec_1525478,Human_Splice_Rec_1525479,Human_Splice_Rec_1525528,Human_Splice_Rec_1525529,Human_Splice_Rec_1525584,Human_Splice_Rec_1525585 RMVar_hsa_circ_15478,RMVar_hsa_circ_323492,RMVar_hsa_circ_337535,RMVar_hsa_circ_343567,RMVar_hsa_circ_73127,RMVar_hsa_circ_301153,RMVar_hsa_circ_72690,RMVar_hsa_circ_60114,RMVar_hsa_circ_167248,RMVar_hsa_circ_5260,RMVar_hsa_circ_167249,RMVar_hsa_circ_76273,RMVar_hsa_circ_167250 71942 RMVar_ID_71942 Human_SNP_ID_558329072 m1A Human chr14 + 64441758 64441758 64441758 CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGACTGGGCGACAGAGCG CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGACTGGGCGACAGAGCG A C MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64441753..64442095 32194978 MeRIP-seq:(Medium) rs181485144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22924529 RMVar_hsa_circ_73389,RMVar_hsa_circ_98039,RMVar_hsa_circ_88169,RMVar_hsa_circ_167254,RMVar_hsa_circ_116338,RMVar_hsa_circ_167259,RMVar_hsa_circ_60441,RMVar_hsa_circ_111871,RMVar_hsa_circ_167260,RMVar_hsa_circ_167265,RMVar_hsa_circ_167264,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_325471,RMVar_hsa_circ_104064,RMVar_hsa_circ_373779,RMVar_hsa_circ_167272,RMVar_hsa_circ_167274,RMVar_hsa_circ_347296,RMVar_hsa_circ_354424,RMVar_hsa_circ_355605,RMVar_hsa_circ_330097,RMVar_hsa_circ_167276,RMVar_hsa_circ_121494,RMVar_hsa_circ_167278,RMVar_hsa_circ_66291,RMVar_hsa_circ_353213,RMVar_hsa_circ_167275,RMVar_hsa_circ_325083,RMVar_hsa_circ_167279 71943 RMVar_ID_71943 Human_SNP_ID_558329073 m1A Human chr14 + 64441758 64441758 64441758 CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGACTGGGCGACAGAGCG CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGACTGGGCGACAGAGCG A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64441753..64442095 32194978 MeRIP-seq:(Medium) rs181485144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22924529 RMVar_hsa_circ_73389,RMVar_hsa_circ_98039,RMVar_hsa_circ_88169,RMVar_hsa_circ_167254,RMVar_hsa_circ_116338,RMVar_hsa_circ_167259,RMVar_hsa_circ_60441,RMVar_hsa_circ_111871,RMVar_hsa_circ_167260,RMVar_hsa_circ_167265,RMVar_hsa_circ_167264,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_325471,RMVar_hsa_circ_104064,RMVar_hsa_circ_373779,RMVar_hsa_circ_167272,RMVar_hsa_circ_167274,RMVar_hsa_circ_347296,RMVar_hsa_circ_354424,RMVar_hsa_circ_355605,RMVar_hsa_circ_330097,RMVar_hsa_circ_167276,RMVar_hsa_circ_121494,RMVar_hsa_circ_167278,RMVar_hsa_circ_66291,RMVar_hsa_circ_353213,RMVar_hsa_circ_167275,RMVar_hsa_circ_325083,RMVar_hsa_circ_167279 71944 RMVar_ID_71944 Human_SNP_ID_558329074 m1A Human chr14 + 64441758 64441758 64441758 CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGACTGGGCGACAGAGCG CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCTCGCCACTGCACTCCAGACTGGGCGACAGAGCG A T MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64441753..64442095 32194978 MeRIP-seq:(Medium) rs181485144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22924529 RMVar_hsa_circ_73389,RMVar_hsa_circ_98039,RMVar_hsa_circ_88169,RMVar_hsa_circ_167254,RMVar_hsa_circ_116338,RMVar_hsa_circ_167259,RMVar_hsa_circ_60441,RMVar_hsa_circ_111871,RMVar_hsa_circ_167260,RMVar_hsa_circ_167265,RMVar_hsa_circ_167264,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_325471,RMVar_hsa_circ_104064,RMVar_hsa_circ_373779,RMVar_hsa_circ_167272,RMVar_hsa_circ_167274,RMVar_hsa_circ_347296,RMVar_hsa_circ_354424,RMVar_hsa_circ_355605,RMVar_hsa_circ_330097,RMVar_hsa_circ_167276,RMVar_hsa_circ_121494,RMVar_hsa_circ_167278,RMVar_hsa_circ_66291,RMVar_hsa_circ_353213,RMVar_hsa_circ_167275,RMVar_hsa_circ_325083,RMVar_hsa_circ_167279 71945 RMVar_ID_71945 Human_SNP_ID_558329754 m1A Human chr14 + 64444359 64444359 64444359 TCCGCAGGCCCGACCGCTTCCTCTTTCCCCACACTCCCCTTGACTTCCAACCCCACTGCTATGGC TCCGCAGGCCCGACCGCTTCCTCTTTCCCCACTCTCCCCTTGACTTCCAACCCCACTGCTATGGC A T MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64444356..64444477 26863196 MeRIP-seq:(Medium) rs991609435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19957314 RMVar_hsa_circ_73389,RMVar_hsa_circ_98039,RMVar_hsa_circ_88169,RMVar_hsa_circ_167254,RMVar_hsa_circ_116338,RMVar_hsa_circ_167259,RMVar_hsa_circ_8496,RMVar_hsa_circ_167260,RMVar_hsa_circ_167265,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_325471,RMVar_hsa_circ_104064,RMVar_hsa_circ_373779,RMVar_hsa_circ_167272,RMVar_hsa_circ_167274,RMVar_hsa_circ_347296,RMVar_hsa_circ_354424,RMVar_hsa_circ_355605,RMVar_hsa_circ_330097,RMVar_hsa_circ_167278,RMVar_hsa_circ_66291,RMVar_hsa_circ_353213,RMVar_hsa_circ_167275,RMVar_hsa_circ_325083,RMVar_hsa_circ_167279,RMVar_hsa_circ_281624,RMVar_hsa_circ_293785,RMVar_hsa_circ_354355,RMVar_hsa_circ_291687,RMVar_hsa_circ_167281,RMVar_hsa_circ_167283,RMVar_hsa_circ_167284,RMVar_hsa_circ_167282,RMVar_hsa_circ_167285,RMVar_hsa_circ_352081 71946 RMVar_ID_71946 Human_SNP_ID_558333007 m1A Human chr14 - 64458148 64458148 64458148 TGCTGGGCACAGTGGCTCACGCCTATAATCCCAGGCTGAGGTGGAGAGGATCACTTGAGGCCAGG TGCTGGGCACAGTGGCTCACGCCTATAATCCCGGGCTGAGGTGGAGAGGATCACTTGAGGCCAGG T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64458146..64458568 32194978 MeRIP-seq:(Medium) rs1427351774 Functional Loss SNV dbSNP153 33..33 33 - - - 71947 RMVar_ID_71947 Human_SNP_ID_558333384 m1A Human chr14 - 64459808 64459808 64459808 TACTTATACTTCCTAACTCCCAGTGGGCCTGAATAGACACTGGCCAGACTTTCAAAGTAGCTTCT TACTTATACTTCCTAACTCCCAGTGGGCCTGAGTAGACACTGGCCAGACTTTCAAAGTAGCTTCT T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:64459765..64459966 32194978 MeRIP-seq:(Medium) rs1252213457 Functional Loss SNV dbSNP153 33..33 33 - - - 71948 RMVar_ID_71948 Human_SNP_ID_558338578 m1A Human chr14 - 64481771 64481771 64481771 TCTCTGCTGTACTTCTGTGTTTGTATGGTTGGACATTTTGAAAACTGGTGAGATTGCACAGTCCC TCTCTGCTGTACTTCTGTGTTTGTATGGTTGGTCATTTTGAAAACTGGTGAGATTGCACAGTCCC T A ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10133848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1086221 GWAS_ID_8759,GWAS_ID_8760,GWAS_ID_8761,GWAS_ID_8762,GWAS_ID_8763,GWAS_ID_8764,GWAS_ID_8765,GWAS_ID_8766,GWAS_ID_8767,GWAS_ID_8768,GWAS_ID_8769,GWAS_ID_8770,GWAS_ID_8771,GWAS_ID_8772,GWAS_ID_8773 71949 RMVar_ID_71949 Human_SNP_ID_558344520 m1A Human chr14 + 64504217 64504217 64504217 GGCGGACTGGGCGAGGTGGGGCATGGCGGGGGAAGTGACTCAGGGCCAGAGGCAGCAGGCCCACG GGCGGACTGGGCGAGGTGGGGCATGGCGGGGGGAGTGACTCAGGGCCAGAGGCAGCAGGCCCACG A G ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:64503974..64504911;chr14:64503960..64504664 26863196 MeRIP-seq:(Medium) rs1044105539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260610,Human_RBP_ID_3467676,Human_RBP_ID_5176848,Human_RBP_ID_5315655,Human_RBP_ID_8078575,Human_RBP_ID_8180913,Human_RBP_ID_8230627,Human_RBP_ID_9417786,Human_RBP_ID_18480394,Human_RBP_ID_22696489,Human_RBP_ID_22711182,Human_RBP_ID_26778201 71950 RMVar_ID_71950 Human_SNP_ID_558344521 m1A Human chr14 + 64504218 64504218 64504218 GCGGACTGGGCGAGGTGGGGCATGGCGGGGGAAGTGACTCAGGGCCAGAGGCAGCAGGCCCACGG GCGGACTGGGCGAGGTGGGGCATGGCGGGGGATGTGACTCAGGGCCAGAGGCAGCAGGCCCACGG A T ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:64504216..64504486 26863196 MeRIP-seq:(Medium) rs1449942484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260610,Human_RBP_ID_3467676,Human_RBP_ID_5176848,Human_RBP_ID_5315655,Human_RBP_ID_8078575,Human_RBP_ID_8180913,Human_RBP_ID_8230627,Human_RBP_ID_9417786,Human_RBP_ID_18480394,Human_RBP_ID_22696489,Human_RBP_ID_22711182,Human_RBP_ID_26778201 71951 RMVar_ID_71951 Human_SNP_ID_558344791 m1A Human chr14 + 64504829 64504829 64504829 GAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGAGCGCCGCGCGCCGCCGCCACTGCAGCTCGCGG GAGCCTCTCCGCGCAGCCCAGCCCGAGCGCCGCGCGCCGCGCGCCGCCGCCACTGCAGCTCGCGG A C ZBTB1 Ensembl:ENSG00000126804 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64504791..64504887 26863196 MeRIP-seq:(Medium) rs957272175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1525730,Human_Splice_Rec_1525736 71952 RMVar_ID_71952 Human_SNP_ID_558344804 m1A Human chr14 + 64504848 64504848 64504848 AGCCCGAGCGCCGAGCGCCGCGCGCCGCCGCCACTGCAGCTCGCGGCCCCTTCGCCTTCGCCCGC AGCCCGAGCGCCGAGCGCCGCGCGCCGCCGCCGCTGCAGCTCGCGGCCCCTTCGCCTTCGCCCGC A G ZBTB1 Ensembl:ENSG00000126804 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:64504809..64504894 26863410 MeRIP-seq:(Medium) rs889789598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449731,Human_RBP_ID_4313699 Human_Splice_Rec_1525730,Human_Splice_Rec_1525736,Human_Splice_Rec_1525737,Human_Splice_Rec_1525741,Human_Splice_Rec_1525745 71953 RMVar_ID_71953 Human_SNP_ID_558392187 m1A Human chr14 + 64704500 64704500 64704500 CGGCTCCGCTCGACTTCCTGCCGGGCGCTGGCAAGCCGCGCGCTGCCTGGGGTCTCCGGGGGCCG CGGCTCCGCTCGACTTCCTGCCGGGCGCTGGCCAGCCGCGCGCTGCCTGGGGTCTCCGGGGGCCG A C PLEKHG3 Ensembl:ENSG00000126822 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr14:64704451..64704591;chr14:64704450..64704654 26863196 MeRIP-seq:(Medium) rs1161631310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308861 RMVar_hsa_circ_102591,RMVar_hsa_circ_167302 71954 RMVar_ID_71954 Human_SNP_ID_558401062 m1A Human chr14 + 64738089 64738089 64738089 GAGAAGGGGGCTGGGCCGGAGCCCCCAGGCTCAGAGGAGGAGGAGGAGGAGCAGGAGGAGAGCCT GAGAAGGGGGCTGGGCCGGAGCCCCCAGGCTCGGAGGAGGAGGAGGAGGAGCAGGAGGAGAGCCT A G PLEKHG3 Ensembl:ENSG00000126822 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64738043..64738166 26863196 MeRIP-seq:(Medium) rs1566713612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813979,Human_RBP_ID_21968992,Human_RBP_ID_22473180 Human_Splice_Rec_1525977 RMVar_hsa_circ_113083,RMVar_hsa_circ_124026,RMVar_hsa_circ_167308,RMVar_hsa_circ_167312,RMVar_hsa_circ_96999,RMVar_hsa_circ_105712,RMVar_hsa_circ_167314,RMVar_hsa_circ_167317 71955 RMVar_ID_71955 Human_SNP_ID_558401111 m1A Human chr14 - 64738188 64738188 64738188 GCGCCCCGGGAGAAAAGTAAAGCGTTGGCCCGATAGTGCCAGCAGTGGAGGGCGGCCAGCAGGGA GCGCCCCGGGAGAAAAGTAAAGCGTTGGCCCGGTAGTGCCAGCAGTGGAGGGCGGCCAGCAGGGA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:64738061..64738212 26863196 MeRIP-seq:(Medium) rs1273272427 Functional Loss SNV dbSNP153 33..33 33 - - - 71956 RMVar_ID_71956 Human_SNP_ID_558401912 m1A Human chr14 + 64741234 64741234 64741234 ACTTCGTGGCAGCTGAGAGCACTGAGGACCTTAAGGCCCTGAGCAGCGAGGAGGAAGAAGAAATG ACTTCGTGGCAGCTGAGAGCACTGAGGACCTTTAGGCCCTGAGCAGCGAGGAGGAAGAAGAAATG A T PLEKHG3 Ensembl:ENSG00000126822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64741183..64741330 26863196 MeRIP-seq:(Medium) rs773369452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8795525,Human_RBP_ID_18979700,Human_RBP_ID_27432233 RMVar_hsa_circ_113083,RMVar_hsa_circ_124026,RMVar_hsa_circ_167308,RMVar_hsa_circ_167312,RMVar_hsa_circ_96999,RMVar_hsa_circ_105712,RMVar_hsa_circ_167314,RMVar_hsa_circ_111989,RMVar_hsa_circ_167317,RMVar_hsa_circ_167318 71957 RMVar_ID_71957 Human_SNP_ID_558402039 m1A Human chr14 + 64741518 64741518 64741518 GCCACAGACTCCCTCAGCTGTCAGCTCTCCCCAGAAGTGGACATCAGTGTGGGGGTGGCCACAGA GCCACAGACTCCCTCAGCTGTCAGCTCTCCCCGGAAGTGGACATCAGTGTGGGGGTGGCCACAGA A G PLEKHG3 Ensembl:ENSG00000126822 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64737365..64741748 32194978 MeRIP-seq:(Medium) rs773465088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113083,RMVar_hsa_circ_124026,RMVar_hsa_circ_167308,RMVar_hsa_circ_167312,RMVar_hsa_circ_96999,RMVar_hsa_circ_105712,RMVar_hsa_circ_167314,RMVar_hsa_circ_111989,RMVar_hsa_circ_167317,RMVar_hsa_circ_167318 71958 RMVar_ID_71958 Human_SNP_ID_558402063 m1A Human chr14 - 64741594 64741594 64741594 CTTGCAGGAAGACCGGTCAGGCTCCACTGGGCAGCCTGGGCTTGGGGGCTCCATCCCATTGACAG CTTGCAGGAAGACCGGTCAGGCTCCACTGGGCCGCCTGGGCTTGGGGGCTCCATCCCATTGACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64741547..64741638 26863196 MeRIP-seq:(Medium) rs760591512 Functional Loss SNV dbSNP153 33..33 33 - - - 71959 RMVar_ID_71959 Human_SNP_ID_558402707 m1A Human chr14 - 64743226 64743226 64743226 CGGGGCCGGCCGCCCCCTGCTCGGCGTGCCTCATCGCGGGAGGCATACTTGGAGCAGAGCTCACG CGGGGCCGGCCGCCCCCTGCTCGGCGTGCCTCCTCGCGGGAGGCATACTTGGAGCAGAGCTCACG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64743176..64743263 26863196 MeRIP-seq:(Medium) rs752690221 Functional Loss SNV dbSNP153 33..33 33 - - - 71960 RMVar_ID_71960 Human_SNP_ID_558412271 m1A Human chr14 - 64775234 64775234 64775234 CAGGCTGCGGGAGGCAGCGGCCGGGAGGCTGCAGCGACTGAGGGACGCCAACGAGGCACAGCAGT CAGGCTGCGGGAGGCAGCGGCCGGGAGGCTGCGGCGACTGAGGGACGCCAACGAGGCACAGCAGT T C SPTB Ensembl:ENSG00000070182 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64775184..64775405 26863196 MeRIP-seq:(Medium) rs927773729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8797870,Human_RBP_ID_9282206,Human_RBP_ID_17117157,Human_RBP_ID_27572176,Human_RBP_ID_27808365,Human_RBP_ID_27837341 71961 RMVar_ID_71961 Human_SNP_ID_558456118 m1A Human chr14 - 64951642 64951642 64951642 TTCTCCTGCAGGGACACTGCAGGGCAGGAGAGATACCAGACCATCACAAAGCAGTACTATCGGCG TTCTCCTGCAGGGACACTGCAGGGCAGGAGAGTTACCAGACCATCACAAAGCAGTACTATCGGCG T A RAB15 Ensembl:ENSG00000139998 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64951141..64957957 32194978 MeRIP-seq:(Medium) rs1255509421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1526346,Human_Splice_Rec_1526347,Human_Splice_Rec_1526360,Human_Splice_Rec_1526361,Human_Splice_Rec_1526372,Human_Splice_Rec_1526373,Human_Splice_Rec_1526384,Human_Splice_Rec_1526385,Human_Splice_Rec_1526398,Human_Splice_Rec_1526399,Human_Splice_Rec_1526414,Human_Splice_Rec_1526415,Human_Splice_Rec_1526428,Human_Splice_Rec_1526429,Human_Splice_Rec_1526438,Human_Splice_Rec_1526439,Human_Splice_Rec_1526450,Human_Splice_Rec_1526451 RMVar_hsa_circ_37271,RMVar_hsa_circ_167324,RMVar_hsa_circ_110583 71962 RMVar_ID_71962 Human_SNP_ID_558464995 m1A Human chr14 - 64986962 64986962 64986962 GATGGAGGGCAATAGTAGGTGAAAGAACTCGGAGAAGCCATGATCAGGAGAGCAGCAGACAGTGT GATGGAGGGCAATAGTAGGTGAAAGAACTCGGGGAAGCCATGATCAGGAGAGCAGCAGACAGTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:64986912..64987046 26863196 MeRIP-seq:(Medium) rs200225795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1275862 71963 RMVar_ID_71963 Human_SNP_ID_558470661 m1A Human chr14 + 65010075 65010075 65010075 TTTGCCTTCACCTCTGCTCTGAATGCTCTTGGAGGTCTCTAGCCCTTCTGTGGTTTGTTGTCTTT TTTGCCTTCACCTCTGCTCTGAATGCTCTTGGGGGTCTCTAGCCCTTCTGTGGTTTGTTGTCTTT A G CHURC1-FNTB,FNTB Ensembl:ENSG00000125954,Ensembl:ENSG00000257365 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:65010009..65010151 26863196 MeRIP-seq:(Medium) rs1048440003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2456,RMVar_hsa_circ_167325,RMVar_hsa_circ_19226,RMVar_hsa_circ_321847,RMVar_hsa_circ_304558,RMVar_hsa_circ_167326,RMVar_hsa_circ_167327 71964 RMVar_ID_71964 Human_SNP_ID_558490771 m1A Human chr14 + 65093813 65093813 65093813 CGTTCCAGTGCATTATGATGAGCCCGTTTGTCAGCCTAGAAGAATGGGAGAAAGAACACATTAGG CGTTCCAGTGCATTATGATGAGCCCGTTTGTCGGCCTAGAAGAATGGGAGAAAGAACACATTAGG A G AL139022.1 Ensembl:ENSG00000259118 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:65093776..65093825 26863196 MeRIP-seq:(Medium) rs1566622633 Functional Loss SNV dbSNP153 33..33 33 - - - 71965 RMVar_ID_71965 Human_SNP_ID_558492893 m1A Human chr14 - 65102392 65102391 65102392 TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTCACCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTC_CCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC GT G MAX Ensembl:ENSG00000125952 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:65102326..65102475 32194978 MeRIP-seq:(Medium) rs1180147243 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_196866,Human_RBP_ID_449893,Human_RBP_ID_4313744,Human_RBP_ID_5418228,Human_RBP_ID_5439483,Human_RBP_ID_5463488,Human_RBP_ID_5494151,Human_RBP_ID_5645796,Human_RBP_ID_8181731,Human_RBP_ID_18936814,Human_RBP_ID_23208730,Human_RBP_ID_23631322,Human_RBP_ID_27808376 Human_Splice_Rec_1526539,Human_Splice_Rec_1526545,Human_Splice_Rec_1526553,Human_Splice_Rec_1526559,Human_Splice_Rec_1526569,Human_Splice_Rec_1526577,Human_Splice_Rec_1526585,Human_Splice_Rec_1526587,Human_Splice_Rec_1526593,Human_Splice_Rec_1526599,Human_Splice_Rec_1526627,Human_Splice_Rec_1526635,Human_Splice_Rec_1526641,Human_Splice_Rec_1526649,Human_Splice_Rec_1526653,Human_Splice_Rec_1526659,Human_Splice_Rec_1526663 71966 RMVar_ID_71966 Human_SNP_ID_558492894 m1A Human chr14 - 65102392 65102392 65102392 TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTCACCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTCCCCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC T G MAX Ensembl:ENSG00000125952 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:65102326..65102475 32194978 MeRIP-seq:(Medium) rs1005278567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196866,Human_RBP_ID_449893,Human_RBP_ID_4313744,Human_RBP_ID_5418228,Human_RBP_ID_5439483,Human_RBP_ID_5463488,Human_RBP_ID_5494151,Human_RBP_ID_5645796,Human_RBP_ID_8181731,Human_RBP_ID_18936814,Human_RBP_ID_23208730,Human_RBP_ID_23631322,Human_RBP_ID_27808376 Human_Splice_Rec_1526539,Human_Splice_Rec_1526545,Human_Splice_Rec_1526553,Human_Splice_Rec_1526559,Human_Splice_Rec_1526569,Human_Splice_Rec_1526577,Human_Splice_Rec_1526585,Human_Splice_Rec_1526587,Human_Splice_Rec_1526593,Human_Splice_Rec_1526599,Human_Splice_Rec_1526627,Human_Splice_Rec_1526635,Human_Splice_Rec_1526641,Human_Splice_Rec_1526649,Human_Splice_Rec_1526653,Human_Splice_Rec_1526659,Human_Splice_Rec_1526663 71967 RMVar_ID_71967 Human_SNP_ID_558492925 m1A Human chr14 - 65102449 65102449 65102449 TGTGAGTGAGAGAGCGAGTGAGTGAGTGAGTGAGTGTGTGTGTGGGGGGGACTCGGCTTGTTGTT TGTGAGTGAGAGAGCGAGTGAGTGAGTGAGTGTGTGTGTGTGTGGGGGGGACTCGGCTTGTTGTT T A MAX Ensembl:ENSG00000125952 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr14:65102350..65102501 26863410 MeRIP-seq:(Medium) rs886050636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196866,Human_RBP_ID_449895,Human_RBP_ID_758316,Human_RBP_ID_880978,Human_RBP_ID_3944555,Human_RBP_ID_5236039,Human_RBP_ID_5286144,Human_RBP_ID_5351741,Human_RBP_ID_5439204,Human_RBP_ID_5523049,Human_RBP_ID_5645797,Human_RBP_ID_6370951,Human_RBP_ID_8407405,Human_RBP_ID_9345011,Human_RBP_ID_17248548,Human_RBP_ID_18457602,Human_RBP_ID_18979704,Human_RBP_ID_22439618,Human_RBP_ID_22472948,Human_RBP_ID_23113618,Human_RBP_ID_23208555,Human_RBP_ID_23631322,Human_RBP_ID_26325167,Human_RBP_ID_27808376 Human_miRNA_ID_1051161 Clinvar_Rec_301 71968 RMVar_ID_71968 Human_SNP_ID_558492933 m1A Human chr14 - 65102469 65102467 65102469 TTGCCCGTGTTGTGTGTGTGTGTGAGTGAGAGAGCGAGTGAGTGAGTGAGTGAGTGTGTGTGTGG TTGCCCGTGTTGTGTGTGTGTGTGAGTGAGAG__CGAGTGAGTGAGTGAGTGAGTGTGTGTGTGG GCT G MAX Ensembl:ENSG00000125952 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:65101505..65102573;chr14:65101578..65102554 26863196 MeRIP-seq:(Medium) rs1325307213 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_196866,Human_RBP_ID_449896,Human_RBP_ID_758316,Human_RBP_ID_880978,Human_RBP_ID_3944555,Human_RBP_ID_4298935,Human_RBP_ID_5236039,Human_RBP_ID_5286144,Human_RBP_ID_5351741,Human_RBP_ID_5523049,Human_RBP_ID_5645798,Human_RBP_ID_6370953,Human_RBP_ID_8407405,Human_RBP_ID_9345011,Human_RBP_ID_17248548,Human_RBP_ID_18457602,Human_RBP_ID_18979704,Human_RBP_ID_22439618,Human_RBP_ID_23113618,Human_RBP_ID_23208555,Human_RBP_ID_23631322,Human_RBP_ID_26325167,Human_RBP_ID_27808376 71969 RMVar_ID_71969 Human_SNP_ID_558619361 m1A Human chr14 - 65616092 65616092 65616092 GAGGAGGGGAAAACACTGTATAATCACCTACCATTTCTGGTCTGTTTCTTGTAATTTTCAATCTG GAGGAGGGGAAAACACTGTATAATCACCTACCGTTTCTGGTCTGTTTCTTGTAATTTTCAATCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:65616059..65616277 32194978 MeRIP-seq:(Medium) rs764201564 Functional Loss SNV dbSNP153 33..33 33 - - - 71970 RMVar_ID_71970 Human_SNP_ID_558650502 m1A Human chr14 + 65742338 65742338 65742338 GGTGTCAACAGGAAATTGGGAAGGACGGGCCTATATCCCTCCTACAAAGTTCGAGAGAAGATAGA GGTGTCAACAGGAAATTGGGAAGGACGGGCCTGTATCCCTCCTACAAAGTTCGAGAGAAGATAGA A G FUT8 Ensembl:ENSG00000033170 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:65742220..65742371 32194978 MeRIP-seq:(Medium) rs779844967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167355,RMVar_hsa_circ_266938,RMVar_hsa_circ_167356,RMVar_hsa_circ_167354 71971 RMVar_ID_71971 Human_SNP_ID_558650503 m1A Human chr14 + 65742338 65742338 65742338 GGTGTCAACAGGAAATTGGGAAGGACGGGCCTATATCCCTCCTACAAAGTTCGAGAGAAGATAGA GGTGTCAACAGGAAATTGGGAAGGACGGGCCTTTATCCCTCCTACAAAGTTCGAGAGAAGATAGA A T FUT8 Ensembl:ENSG00000033170 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:65742220..65742371 32194978 MeRIP-seq:(Medium) rs779844967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167355,RMVar_hsa_circ_266938,RMVar_hsa_circ_167356,RMVar_hsa_circ_167354 71972 RMVar_ID_71972 Human_SNP_ID_558716646 m1A Human chr14 - 66013441 66013441 66013441 AGTTTGATGTTGTTGAAGGAGAAAAGGGTGCGAAGGCAGCAAATGTTACAGGTCCTGGTGGTGTT AGTTTGATGTTGTTGAAGGAGAAAAGGGTGCGGAGGCAGCAAATGTTACAGGTCCTGGTGGTGTT T C YBX1P1 Ensembl:ENSG00000224861 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs878979795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6402910,Human_RBP_ID_17857119 71973 RMVar_ID_71973 Human_SNP_ID_558716793 m1A Human chr14 - 66013873 66013873 66013873 AGAGCGGACCCCAGAGAGCCCTGAGCAGCCCCACCGCCGCCGCCGGCCTAGTTACCGTCACACCC AGAGCGGACCCCAGAGAGCCCTGAGCAGCCCCGCCGCCGCCGCCGGCCTAGTTACCGTCACACCC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:66013773..66013903 26863410 MeRIP-seq:(Medium) rs1451092062 Functional Loss SNV dbSNP153 33..33 33 - - - 71974 RMVar_ID_71974 Human_SNP_ID_558716801 m1A Human chr14 - 66013893 66013893 66013893 TCGATCGGTAGCGGGAGCGGAGAGCGGACCCCAGAGAGCCCTGAGCAGCCCCACCGCCGCCGCCG TCGATCGGTAGCGGGAGCGGAGAGCGGACCCCGGAGAGCCCTGAGCAGCCCCACCGCCGCCGCCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:66013797..66013897 26863410 MeRIP-seq:(Medium) rs1159689602 Functional Loss SNV dbSNP153 33..33 33 - - - 71975 RMVar_ID_71975 Human_SNP_ID_558829982 m1A Human chr14 + 66508198 66508198 66508198 CATCTAGCTGCCTTGGGTCTCGCGCTCCGCAGAGCGTTCCGACACTCTCCGGCCTCGTTCTGCCG CATCTAGCTGCCTTGGGTCTCGCGCTCCGCAGTGCGTTCCGACACTCTCCGGCCTCGTTCTGCCG A T GPHN Ensembl:ENSG00000171723 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr14:66508151..66508425 26863196 MeRIP-seq:(Medium) rs940097893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1275904 71976 RMVar_ID_71976 Human_SNP_ID_558847387 m1A Human chr14 + 66575832 66575832 66575832 ACTGGGGTAGGCCTGGTGTCTGGGTGTCTGGGATCTACTGGAGTGGTCCTAGAGGCTGCATCCGT ACTGGGGTAGGCCTGGTGTCTGGGTGTCTGGGCTCTACTGGAGTGGTCCTAGAGGCTGCATCCGT A C GPHN Ensembl:ENSG00000171723 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:66575826..66575910 26863196 MeRIP-seq:(Medium) rs1158213241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6371932,Human_RBP_ID_9353000,Human_RBP_ID_17118399,Human_RBP_ID_22696612 71977 RMVar_ID_71977 Human_SNP_ID_558980945 m1A Human chr14 + 67116298 67116296 67116299 AAAGAAAAGAAAAAGAAAGAAAGAAAAGAAAAAGAAAGAAAGAAAGAAAAAGAAAGAAAGAAACA AAAGAAAAGAAAAAGAAAGAAAGAAAAGAAA___AAAGAAAGAAAGAAAAAGAAAGAAAGAAACA AAAG A GPHN Ensembl:ENSG00000171723 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:67116263..67116374 26863196 MeRIP-seq:(Medium) rs1479097454 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_12654,RMVar_hsa_circ_69030,RMVar_hsa_circ_332545,RMVar_hsa_circ_76050,RMVar_hsa_circ_5834,RMVar_hsa_circ_326265,RMVar_hsa_circ_338005,RMVar_hsa_circ_167374,RMVar_hsa_circ_69996,RMVar_hsa_circ_167378,RMVar_hsa_circ_46189,RMVar_hsa_circ_278029,RMVar_hsa_circ_314217,RMVar_hsa_circ_273905,RMVar_hsa_circ_167383,RMVar_hsa_circ_167381,RMVar_hsa_circ_21038,RMVar_hsa_circ_167384,RMVar_hsa_circ_329387,RMVar_hsa_circ_167382,RMVar_hsa_circ_313276,RMVar_hsa_circ_167385 71978 RMVar_ID_71978 Human_SNP_ID_559023678 m1A Human chr14 + 67296061 67296061 67296061 AGTGCTATGATGGCAATATGAGAAGAGTGCCAACAGCACCGAGATGTGCCTAATTCTGTTTTGGG AGTGCTATGATGGCAATATGAGAAGAGTGCCAGCAGCACCGAGATGTGCCTAATTCTGTTTTGGG A G MPP5 Ensembl:ENSG00000072415 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:67296032..67296260 26863196 MeRIP-seq:(Medium) rs1474549089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167393,RMVar_hsa_circ_303042,RMVar_hsa_circ_305131,RMVar_hsa_circ_286211,RMVar_hsa_circ_114872,RMVar_hsa_circ_167391,RMVar_hsa_circ_167392,RMVar_hsa_circ_167390,RMVar_hsa_circ_13287,RMVar_hsa_circ_71093,RMVar_hsa_circ_60521,RMVar_hsa_circ_308879,RMVar_hsa_circ_367104,RMVar_hsa_circ_64946,RMVar_hsa_circ_54882,RMVar_hsa_circ_167394,RMVar_hsa_circ_167395 71979 RMVar_ID_71979 Human_SNP_ID_559023698 m1A Human chr14 + 67296131 67296131 67296131 GGGAAGGATGAGGGGAATGGTGAGAAGAAGGAAAAAACATAGAAGGAAATTTAATTTGCTGAGTC GGGAAGGATGAGGGGAATGGTGAGAAGAAGGAGAAAACATAGAAGGAAATTTAATTTGCTGAGTC A G MPP5 Ensembl:ENSG00000072415 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:67296044..67296258 26863196 MeRIP-seq:(Medium) rs1400310999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167393,RMVar_hsa_circ_303042,RMVar_hsa_circ_305131,RMVar_hsa_circ_286211,RMVar_hsa_circ_114872,RMVar_hsa_circ_167391,RMVar_hsa_circ_167392,RMVar_hsa_circ_167390,RMVar_hsa_circ_13287,RMVar_hsa_circ_71093,RMVar_hsa_circ_60521,RMVar_hsa_circ_308879,RMVar_hsa_circ_367104,RMVar_hsa_circ_64946,RMVar_hsa_circ_54882,RMVar_hsa_circ_167394,RMVar_hsa_circ_167395 71980 RMVar_ID_71980 Human_SNP_ID_559025130 m1A Human chr14 - 67302076 67302076 67302076 TCACGAGCCTTTTCTATACGAACTATTTTTACAGTTTCTCCTCCATACTGGCCAATACTTTCATA TCACGAGCCTTTTCTATACGAACTATTTTTACGGTTTCTCCTCCATACTGGCCAATACTTTCATA T C ATP6V1D Ensembl:ENSG00000100554 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:67302026..67302100 26863196 MeRIP-seq:(Medium) rs779470836 Functional Loss SNV dbSNP153 33..33 33 - - - 71981 RMVar_ID_71981 Human_SNP_ID_559029645 m1A Human chr14 + 67321148 67321148 67321148 CGGCAAGCATTCGAGGCAGACATAGCAGCTGGAAAGTTCATTGAGCATGGTGAATTTGAGAAGAA CGGCAAGCATTCGAGGCAGACATAGCAGCTGGCAAGTTCATTGAGCATGGTGAATTTGAGAAGAA A C MPP5 Ensembl:ENSG00000072415 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67321062..67321163 32194978 MeRIP-seq:(Medium) rs374085980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1822762,Human_RBP_ID_26325172 Human_Splice_Rec_1527764,Human_Splice_Rec_1527794 RMVar_hsa_circ_167393,RMVar_hsa_circ_303042,RMVar_hsa_circ_305131,RMVar_hsa_circ_114872,RMVar_hsa_circ_167391,RMVar_hsa_circ_167392,RMVar_hsa_circ_13287,RMVar_hsa_circ_71093,RMVar_hsa_circ_60521,RMVar_hsa_circ_355436,RMVar_hsa_circ_167398,RMVar_hsa_circ_90490,RMVar_hsa_circ_300438,RMVar_hsa_circ_327500,RMVar_hsa_circ_167400,RMVar_hsa_circ_347202,RMVar_hsa_circ_358922 71982 RMVar_ID_71982 Human_SNP_ID_559029646 m1A Human chr14 + 67321148 67321148 67321148 CGGCAAGCATTCGAGGCAGACATAGCAGCTGGAAAGTTCATTGAGCATGGTGAATTTGAGAAGAA CGGCAAGCATTCGAGGCAGACATAGCAGCTGGGAAGTTCATTGAGCATGGTGAATTTGAGAAGAA A G MPP5 Ensembl:ENSG00000072415 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67321062..67321163 32194978 MeRIP-seq:(Medium) rs374085980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1822762,Human_RBP_ID_26325172 Human_Splice_Rec_1527764,Human_Splice_Rec_1527794 RMVar_hsa_circ_167393,RMVar_hsa_circ_303042,RMVar_hsa_circ_305131,RMVar_hsa_circ_114872,RMVar_hsa_circ_167391,RMVar_hsa_circ_167392,RMVar_hsa_circ_13287,RMVar_hsa_circ_71093,RMVar_hsa_circ_60521,RMVar_hsa_circ_355436,RMVar_hsa_circ_167398,RMVar_hsa_circ_90490,RMVar_hsa_circ_300438,RMVar_hsa_circ_327500,RMVar_hsa_circ_167400,RMVar_hsa_circ_347202,RMVar_hsa_circ_358922 71983 RMVar_ID_71983 Human_SNP_ID_559033346 m1A Human chr14 - 67334262 67334262 67334262 AATTTTAAAGCTACAGCTATAGAGACAGTACGAAAATCCTATTAGCTTAAATGTTTCTTTTATGA AATTTTAAAGCTACAGCTATAGAGACAGTACGTAAATCCTATTAGCTTAAATGTTTCTTTTATGA T A ATP6V1D Ensembl:ENSG00000100554 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67334219..67334420 32194978 MeRIP-seq:(Medium) rs966635651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292570 71984 RMVar_ID_71984 Human_SNP_ID_559033509 m1A Human chr14 - 67334856 67334856 67334856 ATCACAAAACTCCATTGTCAACCATAGACTACACTTCATTCCTGAGACGTAAACTGGAAAACTGA ATCACAAAACTCCATTGTCAACCATAGACTACCCTTCATTCCTGAGACGTAAACTGGAAAACTGA T G ATP6V1D Ensembl:ENSG00000100554 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67334819..67334970 32194978 MeRIP-seq:(Medium) rs1449379424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292570 71985 RMVar_ID_71985 Human_SNP_ID_559036696 m1A Human chr14 + 67347422 67347422 67347422 CAAAAAGTTTCACACTTACTGTCAGTTCCTTCATGGTAATGTTCAAATACTGGCAAAGTAACACC CAAAAAGTTTCACACTTACTGTCAGTTCCTTCGTGGTAATGTTCAAATACTGGCAAAGTAACACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:67345793..67347430 32194978 MeRIP-seq:(Medium) rs879024705 Functional Loss SNV dbSNP153 33..33 33 - - - 71986 RMVar_ID_71986 Human_SNP_ID_559038068 m1A Human chr14 - 67353002 67353002 67353002 GACCATCATGAAGGCTCGTTTAAAGGGAGCACAGACAGGTCGAAACCTCCTGAAGAAAAAATCTG GACCATCATGAAGGCTCGTTTAAAGGGAGCACTGACAGGTCGAAACCTCCTGAAGAAAAAATCTG T A ATP6V1D Ensembl:ENSG00000100554 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67352951..67353050 32194978 MeRIP-seq:(Medium) rs1364562185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4299156 Human_Splice_Rec_1527814,Human_Splice_Rec_1527815,Human_Splice_Rec_1527862,Human_Splice_Rec_1527863,Human_Splice_Rec_1527878,Human_Splice_Rec_1527879,Human_Splice_Rec_1527900,Human_Splice_Rec_1527901,Human_Splice_Rec_1527913,Human_Splice_Rec_1527924,Human_Splice_Rec_1527925,Human_Splice_Rec_1527934,Human_Splice_Rec_1527935,Human_Splice_Rec_1527942,Human_Splice_Rec_1527943,Human_Splice_Rec_1527948,Human_Splice_Rec_1527949,Human_Splice_Rec_1527952 RMVar_hsa_circ_88150,RMVar_hsa_circ_167403,RMVar_hsa_circ_362814,RMVar_hsa_circ_292047,RMVar_hsa_circ_355195 71987 RMVar_ID_71987 Human_SNP_ID_559038272 m1A Human chr14 - 67353816 67353816 67353816 CCACTGCAATCCAGCCTGGGTGACAGAGCAAGACCCCATCTCAAAAAATAAGGAGTCGGGCCGGG CCACTGCAATCCAGCCTGGGTGACAGAGCAAGGCCCCATCTCAAAAAATAAGGAGTCGGGCCGGG T C ATP6V1D Ensembl:ENSG00000100554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:67353814..67353954 26863196 MeRIP-seq:(Medium) rs1431463153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88150,RMVar_hsa_circ_167403 71988 RMVar_ID_71988 Human_SNP_ID_559052653 m1A Human chr14 + 67412072 67412072 67412072 TTGAGCACGCCGTCCTCCATGTCGCCGCCCGCACGCCAGGGCCACCCCAGGTGCGCCTTCCCCGC TTGAGCACGCCGTCCTCCATGTCGCCGCCCGCCCGCCAGGGCCACCCCAGGTGCGCCTTCCCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:67412025..67412145 26863196 MeRIP-seq:(Medium) rs1463032128 Functional Loss SNV dbSNP153 33..33 33 - - - 71989 RMVar_ID_71989 Human_SNP_ID_559052663 m1A Human chr14 + 67412088 67412088 67412088 CCATGTCGCCGCCCGCACGCCAGGGCCACCCCAGGTGCGCCTTCCCCGCGCCTCGCGCTCCTCGG CCATGTCGCCGCCCGCACGCCAGGGCCACCCCCGGTGCGCCTTCCCCGCGCCTCGCGCTCCTCGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:67412004..67412130 26863196 MeRIP-seq:(Medium) rs534362123 Functional Loss SNV dbSNP153 33..33 33 - - - 71990 RMVar_ID_71990 Human_SNP_ID_559095462 m1A Human chr14 - 67593316 67593316 67593316 TGGCTCGTTTTTTCTATGTTTTGCAGAGATGCAGTCTCACTATGTTGCCTAGGCTGGTCTTGAAT TGGCTCGTTTTTTCTATGTTTTGCAGAGATGCGGTCTCACTATGTTGCCTAGGCTGGTCTTGAAT T C PIGH Ensembl:ENSG00000100564 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34767169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113561,RMVar_hsa_circ_345399,RMVar_hsa_circ_282693,RMVar_hsa_circ_167419 71991 RMVar_ID_71991 Human_SNP_ID_559097145 m1A Human chr14 + 67600087 67600087 67600087 AGCCACACCGTGCAGGTGACAGCGGTGAGCGAACGCAGCGAGAGCCGAGGGCAGCTGAGGCAGAA AGCCACACCGTGCAGGTGACAGCGGTGAGCGACCGCAGCGAGAGCCGAGGGCAGCTGAGGCAGAA A C lnc-ARG2-1 RNACentral:URS00008C134B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:67600039..67600268 26863196 MeRIP-seq:(Medium) rs1433860784 Functional Loss SNV dbSNP153 33..33 33 - - - 71992 RMVar_ID_71992 Human_SNP_ID_559097205 m1A Human chr14 - 67600215 67600205 67600215 CGCAGTGCAGCGCCGCGCGGTGCGGGCGGCCGAGTGGGGGCGTCATGGAGGATGAGCGGAGCTTT CGCAGTGCAGCGCCGCGCGGTGCGGGCGGCCG__________TCATGGAGGATGAGCGGAGCTTT ACGCCCCCACT A PIGH Ensembl:ENSG00000100564 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:67600190..67600272 26863410 MeRIP-seq:(Medium) rs894408078 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_231565,Human_RBP_ID_4299327 71993 RMVar_ID_71993 Human_SNP_ID_559097222 m1A Human chr14 - 67600239 67600225 67600239 GGCGAGACGGCCAGGGCCGGCGAGCGCAGTGCAGCGCCGCGCGGTGCGGGCGGCCGAGTGGGGGC GGCGAGACGGCCAGGGCCGGCGAGCGCAGTGC______________CGGGCGGCCGAGTGGGGGC GCACCGCGCGGCGCT G PIGH Ensembl:ENSG00000100564 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:67600039..67600263 26863196 MeRIP-seq:(Medium) rs1566782892 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_231565,Human_RBP_ID_4307971 71994 RMVar_ID_71994 Human_SNP_ID_559097237 m1A Human chr14 - 67600239 67600239 67600239 GGCGAGACGGCCAGGGCCGGCGAGCGCAGTGCAGCGCCGCGCGGTGCGGGCGGCCGAGTGGGGGC GGCGAGACGGCCAGGGCCGGCGAGCGCAGTGCGGCGCCGCGCGGTGCGGGCGGCCGAGTGGGGGC T C PIGH Ensembl:ENSG00000100564 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:67600039..67600263 26863196 MeRIP-seq:(Medium) rs1232692820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231565,Human_RBP_ID_4307971 71995 RMVar_ID_71995 Human_SNP_ID_559101775 m1A Human chr14 + 67620024 67620024 67620024 CAGCCTCTCGCGTCTCCTCCAGACGCGAGTGCATTCCATCCTGAAGAAATCCGTCCACTCCGTGG CAGCCTCTCGCGTCTCCTCCAGACGCGAGTGCGTTCCATCCTGAAGAAATCCGTCCACTCCGTGG A G ARG2 Ensembl:ENSG00000081181 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17185189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9323798 Human_Splice_Rec_1528387,Human_Splice_Rec_1528401,Human_Splice_Rec_1528409 71996 RMVar_ID_71996 Human_SNP_ID_559109010 m1A Human chr14 + 67650722 67650722 67650722 GTTTTGTCACACTTTGTTCTTCCAGGGTTGCTATCAGCACTGGATCTTGTTGAAGTCAATCCTCA GTTTTGTCACACTTTGTTCTTCCAGGGTTGCTGTCAGCACTGGATCTTGTTGAAGTCAATCCTCA A G ARG2 Ensembl:ENSG00000081181 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67646983..67651017 32194978 MeRIP-seq:(Medium) rs189159556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880561,Human_RBP_ID_4299357,Human_RBP_ID_17248556,Human_RBP_ID_21887117,Human_RBP_ID_22438524,Human_RBP_ID_22758002 Human_Splice_Rec_1528400,Human_Splice_Rec_1528420 71997 RMVar_ID_71997 Human_SNP_ID_559109011 m1A Human chr14 + 67650722 67650722 67650722 GTTTTGTCACACTTTGTTCTTCCAGGGTTGCTATCAGCACTGGATCTTGTTGAAGTCAATCCTCA GTTTTGTCACACTTTGTTCTTCCAGGGTTGCTTTCAGCACTGGATCTTGTTGAAGTCAATCCTCA A T ARG2 Ensembl:ENSG00000081181 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67646983..67651017 32194978 MeRIP-seq:(Medium) rs189159556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880561,Human_RBP_ID_4299357,Human_RBP_ID_17248556,Human_RBP_ID_21887117,Human_RBP_ID_22438524,Human_RBP_ID_22758002 Human_Splice_Rec_1528400,Human_Splice_Rec_1528420 71998 RMVar_ID_71998 Human_SNP_ID_559111445 m1A Human chr14 + 67659921 67659921 67659921 GTGCATAACGTAGCTCCTCCTCCATCTCTGCCAGCTGGGAAGGCAGAAAGTAGTGAGCAGATAGC GTGCATAACGTAGCTCCTCCTCCATCTCTGCCGGCTGGGAAGGCAGAAAGTAGTGAGCAGATAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:67659904..67659975;chr14:67659876..67663056 26863196 MeRIP-seq:(Medium) rs1049964441 Functional Loss SNV dbSNP153 33..33 33 - - - 71999 RMVar_ID_71999 Human_SNP_ID_559112124 m1A Human chr14 - 67662518 67662518 67662518 ATCTATCTTTTCTAGAAGAAAAGAAGAAATTGATCAGGGATTTTGATGAAAAGCAACAGGAAGCA ATCTATCTTTTCTAGAAGAAAAGAAGAAATTGTTCAGGGATTTTGATGAAAAGCAACAGGAAGCA T A VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:67659913..67663150 26863196 MeRIP-seq:(Medium) rs955282750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450242,Human_RBP_ID_1497578,Human_RBP_ID_1822867,Human_RBP_ID_2422822,Human_RBP_ID_9044236,Human_RBP_ID_9369107,Human_RBP_ID_18654510,Human_RBP_ID_27808381 Human_Splice_Rec_1528424,Human_Splice_Rec_1528425,Human_Splice_Rec_1528446,Human_Splice_Rec_1528447,Human_Splice_Rec_1528466,Human_Splice_Rec_1528467,Human_Splice_Rec_1528472,Human_Splice_Rec_1528473,Human_Splice_Rec_1528478,Human_Splice_Rec_1528479,Human_Splice_Rec_1528482,Human_Splice_Rec_1528483 RMVar_hsa_circ_167420,RMVar_hsa_circ_167423,RMVar_hsa_circ_38011,RMVar_hsa_circ_285187,RMVar_hsa_circ_311881,RMVar_hsa_circ_329533,RMVar_hsa_circ_167421,RMVar_hsa_circ_306203,RMVar_hsa_circ_167422,RMVar_hsa_circ_297704,RMVar_hsa_circ_330903 72000 RMVar_ID_72000 Human_SNP_ID_559112127 m1A Human chr14 + 67662521 67662521 67662521 TTCCTGTTGCTTTTCATCAAAATCCCTGATCAATTTCTTCTTTTCTTCTAGAAAAGATAGATAAG TTCCTGTTGCTTTTCATCAAAATCCCTGATCAGTTTCTTCTTTTCTTCTAGAAAAGATAGATAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:67662476..67662550 26863196 MeRIP-seq:(Medium) rs1413854883 Functional Loss SNV dbSNP153 33..33 33 - - - 72001 RMVar_ID_72001 Human_SNP_ID_559112128 m1A Human chr14 + 67662521 67662521 67662521 TTCCTGTTGCTTTTCATCAAAATCCCTGATCAATTTCTTCTTTTCTTCTAGAAAAGATAGATAAG TTCCTGTTGCTTTTCATCAAAATCCCTGATCATTTTCTTCTTTTCTTCTAGAAAAGATAGATAAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:67662476..67662550 26863196 MeRIP-seq:(Medium) rs1413854883 Functional Loss SNV dbSNP153 33..33 33 - - - 72002 RMVar_ID_72002 Human_SNP_ID_559112131 m1A Human chr14 - 67662537 67662537 67662537 TAATAAGCATTTGAAACTTATCTATCTTTTCTAGAAGAAAAGAAGAAATTGATCAGGGATTTTGA TAATAAGCATTTGAAACTTATCTATCTTTTCTGGAAGAAAAGAAGAAATTGATCAGGGATTTTGA T C VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:67659913..67663056 26863410 MeRIP-seq:(Medium) rs1447892523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9044237,Human_RBP_ID_25108901,Human_RBP_ID_27808381 Human_Splice_Rec_1528425,Human_Splice_Rec_1528447,Human_Splice_Rec_1528467,Human_Splice_Rec_1528473,Human_Splice_Rec_1528479,Human_Splice_Rec_1528483 RMVar_hsa_circ_167420,RMVar_hsa_circ_167423,RMVar_hsa_circ_38011,RMVar_hsa_circ_311881,RMVar_hsa_circ_167421,RMVar_hsa_circ_306203,RMVar_hsa_circ_330903 72003 RMVar_ID_72003 Human_SNP_ID_559114998 m1A Human chr14 - 67674378 67674378 67674378 GGGTGCCCGAGCGGCTGCTGGGGACGGCGGGGACCGGTGAGGCGGGGGTGGGCCACGCCGTGGGG GGGTGCCCGAGCGGCTGCTGGGGACGGCGGGGTCCGGTGAGGCGGGGGTGGGCCACGCCGTGGGG T A VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:67674376..67674831 32194978 MeRIP-seq:(Medium) rs531152724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9369108,Human_RBP_ID_26808102,Human_RBP_ID_27808947 Human_Splice_Rec_1528423,Human_Splice_Rec_1528443,Human_Splice_Rec_1528457 72004 RMVar_ID_72004 Human_SNP_ID_559114999 m1A Human chr14 - 67674378 67674378 67674378 GGGTGCCCGAGCGGCTGCTGGGGACGGCGGGGACCGGTGAGGCGGGGGTGGGCCACGCCGTGGGG GGGTGCCCGAGCGGCTGCTGGGGACGGCGGGGGCCGGTGAGGCGGGGGTGGGCCACGCCGTGGGG T C VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:67674376..67674831 32194978 MeRIP-seq:(Medium) rs531152724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9369108,Human_RBP_ID_26808102,Human_RBP_ID_27808947 Human_Splice_Rec_1528423,Human_Splice_Rec_1528443,Human_Splice_Rec_1528457 72005 RMVar_ID_72005 Human_SNP_ID_559115066 m1A Human chr14 + 67674495 67674495 67674495 CTCCGAGGAGGCGGCGGAGGAGGCCATGGCGCAGGCCGCGCTGGAGCAGCGGCCACCGAGATTCG CTCCGAGGAGGCGGCGGAGGAGGCCATGGCGCGGGCCGCGCTGGAGCAGCGGCCACCGAGATTCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:67674452..67674563;chr14:67674445..67674591 26863196 MeRIP-seq:(Medium) rs945964003 Functional Loss SNV dbSNP153 33..33 33 - - - 72006 RMVar_ID_72006 Human_SNP_ID_559118698 m1A Human chr14 - 67690260 67690260 67690260 TCTACAATGCAGGCCTGGCCTACTGTCACAGCAAGCTAGCCAACATCCTCTTCACCCAGGAACTG TCTACAATGCAGGCCTGGCCTACTGTCACAGCCAGCTAGCCAACATCCTCTTCACCCAGGAACTG T G RDH11,AL049779.1 Ensembl:ENSG00000072042,Ensembl:ENSG00000258466 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67686250..67690404 32194978 MeRIP-seq:(Medium) rs774388246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38810,Human_RBP_ID_22757895,Human_RBP_ID_22798134 Human_Splice_Rec_1528461,Human_Splice_Rec_1528475,Human_Splice_Rec_1528481,Human_Splice_Rec_1528491,Human_Splice_Rec_1528503,Human_Splice_Rec_1528507,Human_Splice_Rec_1528523,Human_Splice_Rec_1528531,Human_Splice_Rec_1528543,Human_Splice_Rec_1528549 Human_miRNA_ID_2466942 RMVar_hsa_circ_167426,RMVar_hsa_circ_167424,RMVar_hsa_circ_110732,RMVar_hsa_circ_279340,RMVar_hsa_circ_289598,RMVar_hsa_circ_271947,RMVar_hsa_circ_167427,RMVar_hsa_circ_167430,RMVar_hsa_circ_167428,RMVar_hsa_circ_167425,RMVar_hsa_circ_311927,RMVar_hsa_circ_313363,RMVar_hsa_circ_376733,RMVar_hsa_circ_167431,RMVar_hsa_circ_167429 72007 RMVar_ID_72007 Human_SNP_ID_559118952 m1A Human chr14 + 67691199 67691197 67691200 CAAAGCCATCTGCTGTCTTCGAGTACGGACACATCATCACTCCTGCATTGTTGATCAAAACGTGG CAAAGCCATCTGCTGTCTTCGAGTACGGACA___CATCACTCCTGCATTGTTGATCAAAACGTGG ACAT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67691148..67691348 32194978 MeRIP-seq:(Medium) rs777748861 Functional Loss DEL dbSNP153 32..34 33 - - - 72008 RMVar_ID_72008 Human_SNP_ID_559120126 m1A Human chr14 - 67695707 67695707 67695707 GAGCATCCCGCTCTGGTGCCGCTGCAGCCGGCAGAGATGGTTGAGCTCATGTTCCCGCTGTTGCT GAGCATCCCGCTCTGGTGCCGCTGCAGCCGGCTGAGATGGTTGAGCTCATGTTCCCGCTGTTGCT T A RDH11 Ensembl:ENSG00000072042 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:67695580..67695712 26863196 MeRIP-seq:(Medium) rs201458765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450303,Human_RBP_ID_1276027,Human_RBP_ID_4299435,Human_RBP_ID_18417994 Human_Splice_Rec_1528485,Human_Splice_Rec_1528495,Human_Splice_Rec_1528513,Human_Splice_Rec_1528521,Human_Splice_Rec_1528535,Human_Splice_Rec_1528541,Human_Splice_Rec_1528545,Human_Splice_Rec_1528551,Human_Splice_Rec_1528557 72009 RMVar_ID_72009 Human_SNP_ID_559120127 m1A Human chr14 - 67695707 67695707 67695707 GAGCATCCCGCTCTGGTGCCGCTGCAGCCGGCAGAGATGGTTGAGCTCATGTTCCCGCTGTTGCT GAGCATCCCGCTCTGGTGCCGCTGCAGCCGGCGGAGATGGTTGAGCTCATGTTCCCGCTGTTGCT T C RDH11 Ensembl:ENSG00000072042 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:67695580..67695712 26863196 MeRIP-seq:(Medium) rs201458765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450303,Human_RBP_ID_1276027,Human_RBP_ID_4299435,Human_RBP_ID_18417994 Human_Splice_Rec_1528485,Human_Splice_Rec_1528495,Human_Splice_Rec_1528513,Human_Splice_Rec_1528521,Human_Splice_Rec_1528535,Human_Splice_Rec_1528541,Human_Splice_Rec_1528545,Human_Splice_Rec_1528551,Human_Splice_Rec_1528557 72010 RMVar_ID_72010 Human_SNP_ID_559139685 m1A Human chr14 - 67775955 67775953 67775956 GCAGACTCTCCAGCAGCTGCTGGTTGGACAGGAGATTGGCTTCACTATGGACGAGGTGGACTCAC GCAGACTCTCCAGCAGCTGCTGGTTGGACAG___ATTGGCTTCACTATGGACGAGGTGGACTCAC TCTC T ZFYVE26 Ensembl:ENSG00000072121 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67775016..67775961 32194978 MeRIP-seq:(Medium) rs1555396056 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9370197 Human_Splice_Rec_1528673,Human_Splice_Rec_1528751,Human_Splice_Rec_1528833,Human_Splice_Rec_1528931 Clinvar_Rec_302 RMVar_hsa_circ_9556,RMVar_hsa_circ_17051,RMVar_hsa_circ_112870,RMVar_hsa_circ_167438,RMVar_hsa_circ_98600,RMVar_hsa_circ_167442,RMVar_hsa_circ_167445,RMVar_hsa_circ_93852,RMVar_hsa_circ_12177,RMVar_hsa_circ_348854,RMVar_hsa_circ_123129,RMVar_hsa_circ_167450,RMVar_hsa_circ_19825,RMVar_hsa_circ_17226,RMVar_hsa_circ_76032,RMVar_hsa_circ_167452 72011 RMVar_ID_72011 Human_SNP_ID_559142384 m1A Human chr14 - 67786235 67786235 67786235 TTTTTGCATTCCCTCTTCCTTCATCTATTTCCAGGTCGACGGATAGACCACGTACTCCTAAATGC TTTTTGCATTCCCTCTTCCTTCATCTATTTCCGGGTCGACGGATAGACCACGTACTCCTAAATGC T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67786197..67789399 32194978 MeRIP-seq:(Medium) rs1470672632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25123393 Clinvar_Rec_303 RMVar_hsa_circ_123129,RMVar_hsa_circ_167450,RMVar_hsa_circ_19825,RMVar_hsa_circ_124322,RMVar_hsa_circ_76032,RMVar_hsa_circ_167452,RMVar_hsa_circ_107843,RMVar_hsa_circ_167453,RMVar_hsa_circ_167454 72012 RMVar_ID_72012 Human_SNP_ID_559143434 m1A Human chr14 + 67790621 67790621 67790621 CCAATGGCCTGTAGAGTTGAGCGGCCACTGCCAGTTCTCCGAATGGTGCTGCTACCCGCATCTGA CCAATGGCCTGTAGAGTTGAGCGGCCACTGCCTGTTCTCCGAATGGTGCTGCTACCCGCATCTGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67789597..67793654 32194978 MeRIP-seq:(Medium) rs1196117490 Functional Loss SNV dbSNP153 33..33 33 - - - 72013 RMVar_ID_72013 Human_SNP_ID_559145390 m1A Human chr14 - 67798395 67798395 67798395 GTTTGAGGTCCCCATCAGAGAGCCCTCAGCACATAGCACATCCTGAAAGGAAGTCAGAACGGGGT GTTTGAGGTCCCCATCAGAGAGCCCTCAGCACGTAGCACATCCTGAAAGGAAGTCAGAACGGGGT T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67798298..67798448 32194978 MeRIP-seq:(Medium) rs756568888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_624144,Human_miRNA_ID_1331587 RMVar_hsa_circ_123129,RMVar_hsa_circ_167450,RMVar_hsa_circ_19825,RMVar_hsa_circ_124322,RMVar_hsa_circ_91763,RMVar_hsa_circ_107843,RMVar_hsa_circ_167453,RMVar_hsa_circ_167454,RMVar_hsa_circ_358326,RMVar_hsa_circ_360145,RMVar_hsa_circ_322631,RMVar_hsa_circ_267136,RMVar_hsa_circ_87212,RMVar_hsa_circ_167455,RMVar_hsa_circ_167456 72014 RMVar_ID_72014 Human_SNP_ID_559305480 m1A Human chr14 - 68510133 68510133 68510133 TGGGGAGTGGCAGTAGGGGAGACAGATCCTGGAAGGCACAGAAACTGCTCCCCACTCAGCAGTGG TGGGGAGTGGCAGTAGGGGAGACAGATCCTGGGAGGCACAGAAACTGCTCCCCACTCAGCAGTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:68510036..68510163 26863196 MeRIP-seq:(Medium) rs756424884 Functional Loss SNV dbSNP153 33..33 33 - - - 72015 RMVar_ID_72015 Human_SNP_ID_559371842 m1A Human chr14 - 68788941 68788938 68788941 GGTGGCACCTCTCCACCTGTACCCGCCCCCCCACCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGTGGCACCTCTCCACCTGTACCCGCCCCCCC___CCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGGT G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68788899..68789148 32194978 MeRIP-seq:(Medium) rs74708775 Functional Loss DEL dbSNP153 33..35 33 - - - Human_miRNA_ID_1702040 72016 RMVar_ID_72016 Human_SNP_ID_559371846 m1A Human chr14 - 68788941 68788939 68788941 GGTGGCACCTCTCCACCTGTACCCGCCCCCCCACCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGTGGCACCTCTCCACCTGTACCCGCCCCCCC__CCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGT G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68788899..68789148 32194978 MeRIP-seq:(Medium) rs1294094521 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1702040 72017 RMVar_ID_72017 Human_SNP_ID_559371849 m1A Human chr14 - 68788941 68788940 68788941 GGTGGCACCTCTCCACCTGTACCCGCCCCCCCACCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGTGGCACCTCTCCACCTGTACCCGCCCCCCC_CCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GT G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68788899..68789148 32194978 MeRIP-seq:(Medium) rs1566559151 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_1702040 72018 RMVar_ID_72018 Human_SNP_ID_559371851 m1A Human chr14 - 68788941 68788941 68788941 GGTGGCACCTCTCCACCTGTACCCGCCCCCCCACCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGTGGCACCTCTCCACCTGTACCCGCCCCCCCGCCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT T C ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68788899..68789148 32194978 MeRIP-seq:(Medium) rs1038895434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1702040 72019 RMVar_ID_72019 Human_SNP_ID_559371852 m1A Human chr14 - 68788941 68788941 68788941 GGTGGCACCTCTCCACCTGTACCCGCCCCCCCACCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT GGTGGCACCTCTCCACCTGTACCCGCCCCCCCCCCCCCCCCACCCCTGCCCCTTGGAAGAGTTGT T G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68788899..68789148 32194978 MeRIP-seq:(Medium) rs1038895434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1702040 72020 RMVar_ID_72020 Human_SNP_ID_559371997 m1A Human chr14 - 68789429 68789429 68789429 CTACCCATCCCATTCCCCACAGGCCCTACATTAACAAGGTTAAGCTCAACCCCTTTCCCCCAGCA CTACCCATCCCATTCCCCACAGGCCCTACATTCACAAGGTTAAGCTCAACCCCTTTCCCCCAGCA T G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:68789378..68789679 26863196 MeRIP-seq:(Medium) rs762729438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2423726,Human_RBP_ID_5127699,Human_RBP_ID_17076478,Human_RBP_ID_17363357,Human_RBP_ID_17479992,Human_RBP_ID_18936843,Human_RBP_ID_27432389 72021 RMVar_ID_72021 Human_SNP_ID_559372056 m1A Human chr14 + 68789598 68789598 68789598 GGGCAGGCGTCTTGAGTTGTCCAAGGTCGGGGAGTCTGAGCCACTGTGGCTGCTGCTGGAGCTGC GGGCAGGCGTCTTGAGTTGTCCAAGGTCGGGGTGTCTGAGCCACTGTGGCTGCTGCTGGAGCTGC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:68789551..68789800 26863196 MeRIP-seq:(Medium) rs1199127881 Functional Loss SNV dbSNP153 33..33 33 - - - 72022 RMVar_ID_72022 Human_SNP_ID_559372082 m1A Human chr14 + 68789697 68789697 68789697 AGGGCTGGGGGGAGAGTCAAACATGTGAGGGGACTCGGACATGGGCCGGAAGAGGAAGGTGGTCG AGGGCTGGGGGGAGAGTCAAACATGTGAGGGGGCTCGGACATGGGCCGGAAGAGGAAGGTGGTCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:68789551..68789900 26863196 MeRIP-seq:(Medium) rs957069493 Functional Loss SNV dbSNP153 33..33 33 - - - 72023 RMVar_ID_72023 Human_SNP_ID_559372084 m1A Human chr14 - 68789699 68789699 68789699 CCCGACCACCTTCCTCTTCCGGCCCATGTCCGAGTCCCCTCACATGTTTGACTCTCCCCCCAGCC CCCGACCACCTTCCTCTTCCGGCCCATGTCCGGGTCCCCTCACATGTTTGACTCTCCCCCCAGCC T C ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr14:68789326..68790157;chr14:68789601..68789875 26863196 MeRIP-seq:(Medium) rs772219434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450400,Human_RBP_ID_12397559,Human_RBP_ID_17481156,Human_RBP_ID_22649578 72024 RMVar_ID_72024 Human_SNP_ID_559372098 m1A Human chr14 - 68789724 68789724 68789724 GCATGGGGCTGCCCGGGGGTGGCTCCCCGACCACCTTCCTCTTCCGGCCCATGTCCGAGTCCCCT GCATGGGGCTGCCCGGGGGTGGCTCCCCGACCGCCTTCCTCTTCCGGCCCATGTCCGAGTCCCCT T C ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:68789675..68789777 26863196 MeRIP-seq:(Medium) rs765865743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450400,Human_RBP_ID_999185,Human_RBP_ID_17363361,Human_RBP_ID_17481156,Human_RBP_ID_22044588,Human_RBP_ID_22438750 Human_miRNA_ID_447070,Human_miRNA_ID_450953,Human_miRNA_ID_1361880 72025 RMVar_ID_72025 Human_SNP_ID_559372117 m1A Human chr14 - 68789754 68789754 68789754 GCCAGGAGCTGGCAAGCCTCTTTGCCCCTAGCATGGGGCTGCCCGGGGGTGGCTCCCCGACCACC GCCAGGAGCTGGCAAGCCTCTTTGCCCCTAGCTTGGGGCTGCCCGGGGGTGGCTCCCCGACCACC T A ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:68789726..68789800 26863196 MeRIP-seq:(Medium) rs1350916615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12397560,Human_RBP_ID_17363361,Human_RBP_ID_17479998,Human_RBP_ID_22044589 72026 RMVar_ID_72026 Human_SNP_ID_559372142 m1A Human chr14 + 68789822 68789822 68789822 AGAAGGCAAAAGGGTTATTGGTGCCATCGGGCAGGGTAGGTGAGCCCAGGAGGTCATCGGCGCTC AGAAGGCAAAAGGGTTATTGGTGCCATCGGGCGGGGTAGGTGAGCCCAGGAGGTCATCGGCGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:68789773..68789973 26863196 MeRIP-seq:(Medium) rs928821903 Functional Loss SNV dbSNP153 33..33 33 - - - 72027 RMVar_ID_72027 Human_SNP_ID_559372221 m1A Human chr14 - 68790072 68790072 68790072 GCCACCCCAAGTACAAGACGGAGCTGTGCCGCACCTTCCACACCATCGGCTTTTGCCCCTACGGG GCCACCCCAAGTACAAGACGGAGCTGTGCCGCCCCTTCCACACCATCGGCTTTTGCCCCTACGGG T G ZFP36L1 Ensembl:ENSG00000185650 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68789329..68790156 26863196 MeRIP-seq:(Medium) rs776253509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5493808,Human_RBP_ID_6376005,Human_RBP_ID_8408267,Human_RBP_ID_8795676,Human_RBP_ID_17247718,Human_RBP_ID_17480001,Human_RBP_ID_26808106,Human_RBP_ID_27432403 Human_miRNA_ID_447071,Human_miRNA_ID_450954,Human_miRNA_ID_1361881 72028 RMVar_ID_72028 Human_SNP_ID_559372330 m1A Human chr14 + 68790412 68790412 68790412 AGGGTGACTGAGTGCCTCCGAGGGAAGCCCCCACCAGCAGGGGTGCCCACTGCCTTTCTGTCCAG AGGGTGACTGAGTGCCTCCGAGGGAAGCCCCCCCCAGCAGGGGTGCCCACTGCCTTTCTGTCCAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68789445..68790500 32194978 MeRIP-seq:(Medium) rs1438287070 Functional Loss SNV dbSNP153 33..33 33 - - - 72029 RMVar_ID_72029 Human_SNP_ID_559372356 m1A Human chr14 + 68790490 68790490 68790490 GCACTGGGAGCACTATAGTTGAGCATCTTGTTACCCTGGAGAGAGAAGAGAAAGGATGGTAAGGA GCACTGGGAGCACTATAGTTGAGCATCTTGTTTCCCTGGAGAGAGAAGAGAAAGGATGGTAAGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68790487..68791176 26863196 MeRIP-seq:(Medium) rs1566560146 Functional Loss SNV dbSNP153 33..33 33 - - - 72030 RMVar_ID_72030 Human_SNP_ID_559372565 m1A Human chr14 + 68791228 68791228 68791228 AGCCCTAGCCCACCCCGCCCCCTTCACTGAGAAGATGCCTTTGCAATTAGTCTTTTGGCTGCAAG AGCCCTAGCCCACCCCGCCCCCTTCACTGAGACGATGCCTTTGCAATTAGTCTTTTGGCTGCAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68791225..68793062 32194978 MeRIP-seq:(Medium) rs1566560386 Functional Loss SNV dbSNP153 33..33 33 - - - 72031 RMVar_ID_72031 Human_SNP_ID_559374233 m1A Human chr14 - 68795869 68795869 68795869 GCTCCCGCCCTCGGGCCCTCACCGCGGCGGGGACGCCGGGTCAGCGAAGGGTTAAGGGACTCGCT GCTCCCGCCCTCGGGCCCTCACCGCGGCGGGGGCGCCGGGTCAGCGAAGGGTTAAGGGACTCGCT T C ZFP36L1 Ensembl:ENSG00000185650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68795824..68796113 26863196 MeRIP-seq:(Medium) rs942664034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1276163,Human_RBP_ID_1362089,Human_RBP_ID_3468698,Human_RBP_ID_5463507,Human_RBP_ID_9281852,Human_RBP_ID_22711686,Human_RBP_ID_23126989,Human_RBP_ID_24530724,Human_RBP_ID_26756458 72032 RMVar_ID_72032 Human_SNP_ID_559378999 m1A Human chr14 - 68816762 68816762 68816762 CGGGAACGAAGCCGTAGCGAGAACCTCGCCCCACGCCGCAGCCTCCTGCAGCAGCGTCGGCTCGC CGGGAACGAAGCCGTAGCGAGAACCTCGCCCCGCGCCGCAGCCTCCTGCAGCAGCGTCGGCTCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:68816712..68816792 26863196 MeRIP-seq:(Medium) rs914324720 Functional Loss SNV dbSNP153 33..33 33 - - - 72033 RMVar_ID_72033 Human_SNP_ID_559392724 m1A Human chr14 + 68874375 68874375 68874375 CATAAAATATTTTCATGGACAAGTGAGCTAGCAAACACACATGCACCAATGTGCCTTTTGACAAG CATAAAATATTTTCATGGACAAGTGAGCTAGCCAACACACATGCACCAATGTGCCTTTTGACAAG A C HSALNG0102127 RNACentral:URS0000EA9842 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:68874276..68874450 32194978 MeRIP-seq:(Medium) rs1566580987 Functional Loss SNV dbSNP153 33..33 33 - - - 72034 RMVar_ID_72034 Human_SNP_ID_559392726 m1A Human chr14 - 68874384 68874384 68874384 GGGGGTACTCTTGTCAAAAGGCACATTGGTGCATGTGTGTTTGCTAGCTCACTTGTCCATGAAAA GGGGGTACTCTTGTCAAAAGGCACATTGGTGCTTGTGTGTTTGCTAGCTCACTTGTCCATGAAAA T A ACTN1 Ensembl:ENSG00000072110 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68874276..68874425 32194978 MeRIP-seq:(Medium) rs891764886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450407,Human_RBP_ID_1497839,Human_RBP_ID_1823225,Human_RBP_ID_3458715,Human_RBP_ID_4299558 Human_miRNA_ID_1475297,Human_miRNA_ID_1480257 72035 RMVar_ID_72035 Human_SNP_ID_559392727 m1A Human chr14 - 68874384 68874384 68874384 GGGGGTACTCTTGTCAAAAGGCACATTGGTGCATGTGTGTTTGCTAGCTCACTTGTCCATGAAAA GGGGGTACTCTTGTCAAAAGGCACATTGGTGCGTGTGTGTTTGCTAGCTCACTTGTCCATGAAAA T C ACTN1 Ensembl:ENSG00000072110 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68874276..68874425 32194978 MeRIP-seq:(Medium) rs891764886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450407,Human_RBP_ID_1497839,Human_RBP_ID_1823225,Human_RBP_ID_3458715,Human_RBP_ID_4299558 Human_miRNA_ID_1475297,Human_miRNA_ID_1480257 72036 RMVar_ID_72036 Human_SNP_ID_559392841 m1A Human chr14 + 68874818 68874818 68874818 GCAGGAGATGGGCGACGGCGGAGGTGCAAGGCAGGGCACGGCGCACAAGACGAGGGCGGCCGGGC GCAGGAGATGGGCGACGGCGGAGGTGCAAGGCTGGGCACGGCGCACAAGACGAGGGCGGCCGGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:68874701..68875045 26863196 MeRIP-seq:(Medium) rs1312467312 Functional Loss SNV dbSNP153 33..33 33 - - - 72037 RMVar_ID_72037 Human_SNP_ID_559392855 m1A Human chr14 + 68874832 68874832 68874832 ACGGCGGAGGTGCAAGGCAGGGCACGGCGCACAAGACGAGGGCGGCCGGGCGGGGTGGATTAGAG ACGGCGGAGGTGCAAGGCAGGGCACGGCGCACCAGACGAGGGCGGCCGGGCGGGGTGGATTAGAG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:68874701..68874950 26863196 MeRIP-seq:(Medium) rs1325620623 Functional Loss SNV dbSNP153 33..33 33 - - - 72038 RMVar_ID_72038 Human_SNP_ID_559392903 m1A Human chr14 - 68874905 68874905 68874905 CACCGGCCCCGACTCCGTGCCAGGTGCTCTGGACTACATGTCCTTCTCCACGGCGCTGTACGGCG CACCGGCCCCGACTCCGTGCCAGGTGCTCTGGGCTACATGTCCTTCTCCACGGCGCTGTACGGCG T C ACTN1 Ensembl:ENSG00000072110 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:68874526..68875041 32194978 MeRIP-seq:(Medium) rs1394713693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18654942,Human_RBP_ID_26808109 72039 RMVar_ID_72039 Human_SNP_ID_559393979 m1A Human chr14 + 68878823 68878823 68878823 AGTAGGTTGCCATGAAAGACAGCAGAGGGCAGAGGGTGGACCAGTGATGGGGCAGACAGAGACAG AGTAGGTTGCCATGAAAGACAGCAGAGGGCAGTGGGTGGACCAGTGATGGGGCAGACAGAGACAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:68878821..68878921 32194978 MeRIP-seq:(Medium) rs960773868 Functional Loss SNV dbSNP153 33..33 33 - - - 72040 RMVar_ID_72040 Human_SNP_ID_559395062 m1A Human chr14 + 68882545 68882545 68882545 TTGCGTAGCCTCTCATTGTGCTGCTGTCGGGCATGCTCCTCCGTCAGAGCTTGGTCCCTCCGAGG TTGCGTAGCCTCTCATTGTGCTGCTGTCGGGCGTGCTCCTCCGTCAGAGCTTGGTCCCTCCGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:68882425..68882584 26863196 MeRIP-seq:(Medium) rs144962043 Functional Loss SNV dbSNP153 33..33 33 - - - 72041 RMVar_ID_72041 Human_SNP_ID_559396976 m1A Human chr14 - 68890240 68890240 68890240 CTGGGGCTGCCTGGAGCAGGTGGAGAAGGGCTATGAGGAGTGGTTGCTGAATGAGATCCGGAGGC CTGGGGCTGCCTGGAGCAGGTGGAGAAGGGCTGTGAGGAGTGGTTGCTGAATGAGATCCGGAGGC T C ACTN1 Ensembl:ENSG00000072110 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:68890190..68890314 26863196 MeRIP-seq:(Medium) rs776405361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4299604,Human_RBP_ID_5353142,Human_RBP_ID_22438761,Human_RBP_ID_27808960 Human_Splice_Rec_1529278,Human_Splice_Rec_1529338,Human_Splice_Rec_1529380,Human_Splice_Rec_1529420,Human_Splice_Rec_1529468 Human_miRNA_ID_2001949,Human_miRNA_ID_2003333,Human_miRNA_ID_2708825 RMVar_hsa_circ_372196,RMVar_hsa_circ_167475,RMVar_hsa_circ_125579,RMVar_hsa_circ_14289,RMVar_hsa_circ_10154,RMVar_hsa_circ_167479,RMVar_hsa_circ_114397,RMVar_hsa_circ_328074,RMVar_hsa_circ_110288,RMVar_hsa_circ_11443,RMVar_hsa_circ_167484,RMVar_hsa_circ_167483,RMVar_hsa_circ_311670,RMVar_hsa_circ_318953,RMVar_hsa_circ_321718,RMVar_hsa_circ_60358,RMVar_hsa_circ_167485,RMVar_hsa_circ_167486 72042 RMVar_ID_72042 Human_SNP_ID_559399149 m1A Human chr14 - 68899065 68899054 68899065 GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTGAGGTGTGTGTGGTGTGAGGTGTGGCATGTGTGT GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTG___________GTGTGAGGTGTGGCATGTGTGT CCACACACACCT C ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68898825..68899672 26863196 MeRIP-seq:(Medium) rs1482269413 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_5286151,Human_RBP_ID_5645805,Human_RBP_ID_8180923,Human_RBP_ID_17248930,Human_RBP_ID_23632994 RMVar_hsa_circ_372196,RMVar_hsa_circ_167475,RMVar_hsa_circ_125579,RMVar_hsa_circ_10154,RMVar_hsa_circ_167479,RMVar_hsa_circ_114397,RMVar_hsa_circ_167484,RMVar_hsa_circ_318953,RMVar_hsa_circ_60358 72043 RMVar_ID_72043 Human_SNP_ID_559399152 m1A Human chr14 - 68899065 68899056 68899065 GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTGAGGTGTGTGTGGTGTGAGGTGTGGCATGTGTGT GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTG_________TGGTGTGAGGTGTGGCATGTGTGT ACACACACCT A ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68898825..68899672 26863196 MeRIP-seq:(Medium) rs1233711889 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_5286151,Human_RBP_ID_5645805,Human_RBP_ID_8180923,Human_RBP_ID_17248930,Human_RBP_ID_23632994 RMVar_hsa_circ_372196,RMVar_hsa_circ_167475,RMVar_hsa_circ_125579,RMVar_hsa_circ_10154,RMVar_hsa_circ_167479,RMVar_hsa_circ_114397,RMVar_hsa_circ_167484,RMVar_hsa_circ_318953,RMVar_hsa_circ_60358 72044 RMVar_ID_72044 Human_SNP_ID_559399159 m1A Human chr14 - 68899065 68899065 68899065 GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTGAGGTGTGTGTGGTGTGAGGTGTGGCATGTGTGT GCTGTGGGTGTGAGGTGTGTGTGTGGTGTGTGGGGTGTGTGTGGTGTGAGGTGTGGCATGTGTGT T C ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68898825..68899672 26863196 MeRIP-seq:(Medium) rs1377146394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5286151,Human_RBP_ID_5645805,Human_RBP_ID_8180923,Human_RBP_ID_17248930,Human_RBP_ID_23632994 RMVar_hsa_circ_372196,RMVar_hsa_circ_167475,RMVar_hsa_circ_125579,RMVar_hsa_circ_10154,RMVar_hsa_circ_167479,RMVar_hsa_circ_114397,RMVar_hsa_circ_167484,RMVar_hsa_circ_318953,RMVar_hsa_circ_60358 72045 RMVar_ID_72045 Human_SNP_ID_559405805 m1A Human chr14 - 68925670 68925670 68925670 TGACCACTTGCCCTTCTTGTCTCTGCCCAGACATTCACGGCATGGTGTAACTCCCACCTCCGGAA TGACCACTTGCCCTTCTTGTCTCTGCCCAGACTTTCACGGCATGGTGTAACTCCCACCTCCGGAA T A ACTN1 Ensembl:ENSG00000072110 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68925551..68925675 32194978 MeRIP-seq:(Medium) rs761466378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882933,Human_RBP_ID_3944987 Human_Splice_Rec_1529260,Human_Splice_Rec_1529320,Human_Splice_Rec_1529362,Human_Splice_Rec_1529402,Human_Splice_Rec_1529450,Human_Splice_Rec_1529516,Human_Splice_Rec_1529534,Human_Splice_Rec_1529576,Human_Splice_Rec_1529588,Human_Splice_Rec_1529596,Human_Splice_Rec_1529604 RMVar_hsa_circ_318953,RMVar_hsa_circ_315130,RMVar_hsa_circ_167491,RMVar_hsa_circ_52649,RMVar_hsa_circ_338069,RMVar_hsa_circ_276656,RMVar_hsa_circ_290933,RMVar_hsa_circ_167492,RMVar_hsa_circ_167493 72046 RMVar_ID_72046 Human_SNP_ID_559412508 m1A Human chr14 - 68953275 68953275 68953275 GCTGGAAGAAGGACCAGGAGAGCTTTCAGGACAGGGAAACAACCAGCCCGGCATTGGGGAAACCT GCTGGAAGAAGGACCAGGAGAGCTTTCAGGACCGGGAAACAACCAGCCCGGCATTGGGGAAACCT T G ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:68953273..68953427 26863196 MeRIP-seq:(Medium) rs1347977286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18936860 72047 RMVar_ID_72047 Human_SNP_ID_559414788 m1A Human chr14 + 68962976 68962976 68962976 AGAGCTTGTCCCTCACTGATTCACCAGTCCTCACTGTTGCCCACTCCCAAATATCTTTCACTCCA AGAGCTTGTCCCTCACTGATTCACCAGTCCTCCCTGTTGCCCACTCCCAAATATCTTTCACTCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:68962974..68963072 26863196 MeRIP-seq:(Medium) rs1179298177 Functional Loss SNV dbSNP153 33..33 33 - - - 72048 RMVar_ID_72048 Human_SNP_ID_559418239 m1A Human chr14 - 68977987 68977987 68977987 AGAGGTCAGAAACCACTCGTGGTGGTGGGGGGAGGGCGCCTCAACCCTACCGCTGCTTCCTGCCT AGAGGTCAGAAACCACTCGTGGTGGTGGGGGGGGGGCGCCTCAACCCTACCGCTGCTTCCTGCCT T C ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68977982..68978210 32194978 MeRIP-seq:(Medium) rs913378391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1529603 72049 RMVar_ID_72049 Human_SNP_ID_559418456 m1A Human chr14 + 68978625 68978625 68978625 CGAGCCGGGGTCTCAGCCCCAGCCTGAAGACCACCGCCCCCGAGCACAGCCCACGCGGGGATGGT CGAGCCGGGGTCTCAGCCCCAGCCTGAAGACCGCCGCCCCCGAGCACAGCCCACGCGGGGATGGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:68978624..68979250 32194978 MeRIP-seq:(Medium) rs1164204097 Functional Loss SNV dbSNP153 33..33 33 - - - 72050 RMVar_ID_72050 Human_SNP_ID_559418683 m1A Human chr14 - 68979101 68979101 68979101 CCCCACGCCAGGGCAGCAGCCGTTGCTCAGAGAGAAGGTGGAGGAAGAAATCCAGACCCTAGCAC CCCCACGCCAGGGCAGCAGCCGTTGCTCAGAGTGAAGGTGGAGGAAGAAATCCAGACCCTAGCAC T A ACTN1 Ensembl:ENSG00000072110 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia chr14:68979051..68979300;chr14:68979051..68979275 26863196,32194978 MeRIP-seq:(Medium) rs1566689373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308388,Human_RBP_ID_5463799 72051 RMVar_ID_72051 Human_SNP_ID_559436586 m1A Human chr14 - 69054243 69054243 69054243 CTCTCAACAGCGGGTCTGGCAACTGTCCCAGGACCCAGTCTGATGACAGTGAGGAGAGGAGCCTC CTCTCAACAGCGGGTCTGGCAACTGTCCCAGGGCCCAGTCTGATGACAGTGAGGAGAGGAGCCTC T C DCAF5 Ensembl:ENSG00000139990 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69054151..69054400 32194978 MeRIP-seq:(Medium) rs762968878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8408330 Human_miRNA_ID_2040529,Human_miRNA_ID_3019509 RMVar_hsa_circ_89321,RMVar_hsa_circ_167494 72052 RMVar_ID_72052 Human_SNP_ID_559436745 m1A Human chr14 + 69054728 69054728 69054728 AAGCTTTATAAATTTTTCGCTCAACTGATTCTATGTCAGAAGTTGGTGATGCCCGGCTTGGTTGA AAGCTTTATAAATTTTTCGCTCAACTGATTCTTTGTCAGAAGTTGGTGATGCCCGGCTTGGTTGA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69054677..69054778 32194978 MeRIP-seq:(Medium) rs1389143714 Functional Loss SNV dbSNP153 33..33 33 - - - 72053 RMVar_ID_72053 Human_SNP_ID_559436790 m1A Human chr14 + 69054843 69054843 69054843 GAGGTCATCCACTTTGATCTGGGGGTAATCATAGTTGTCTTCTCCAATGTAAGTGTTGGTGGGCT GAGGTCATCCACTTTGATCTGGGGGTAATCATGGTTGTCTTCTCCAATGTAAGTGTTGGTGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:69054793..69055007;chr14:69054793..69054964 26863196 MeRIP-seq:(Medium) rs768021246 Functional Loss SNV dbSNP153 33..33 33 - - - 72054 RMVar_ID_72054 Human_SNP_ID_559436930 m1A Human chr14 - 69055207 69055207 69055207 CTGGGGCCCCTGCGGGTCACCACCACAAACACAGTAGCCTCAACTCCACCAACACCCACGTGTGA CTGGGGCCCCTGCGGGTCACCACCACAAACACGGTAGCCTCAACTCCACCAACACCCACGTGTGA T C DCAF5 Ensembl:ENSG00000139990 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69055157..69055332 26863196 MeRIP-seq:(Medium) rs1181527873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1823250,Human_RBP_ID_27433839 RMVar_hsa_circ_89321,RMVar_hsa_circ_167494 72055 RMVar_ID_72055 Human_SNP_ID_559458870 m1A Human chr14 - 69153002 69153002 69153002 GCGCGTGAGGCCGAGGGAGGGGCGGCGGCGCGAGCGGCGGCGGCGGCGGTTCCAGCATGAAGAGG GCGCGTGAGGCCGAGGGAGGGGCGGCGGCGCGGGCGGCGGCGGCGGCGGTTCCAGCATGAAGAGG T C DCAF5 Ensembl:ENSG00000139990 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:69152836..69153174 26863196 MeRIP-seq:(Medium) rs911338117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231726,Human_RBP_ID_757654,Human_RBP_ID_880995,Human_RBP_ID_4307979,Human_RBP_ID_5522793,Human_RBP_ID_5645960,Human_RBP_ID_8180944,Human_RBP_ID_9323805,Human_RBP_ID_9417794,Human_RBP_ID_18417997,Human_RBP_ID_18469432,Human_RBP_ID_18936864,Human_RBP_ID_18980754,Human_RBP_ID_21969007,Human_RBP_ID_22045292,Human_RBP_ID_22355326,Human_RBP_ID_22540359 Human_Splice_Rec_1529677,Human_Splice_Rec_1529699 72056 RMVar_ID_72056 Human_SNP_ID_559467165 m1A Human chr14 + 69191583 69191583 69191583 GTGAGCCCGCTGCAGGTGTGCGGCCCAGTCCGAGACAGCAGGTAAGTGAGGCTCAGAAGCCGGCG GTGAGCCCGCTGCAGGTGTGCGGCCCAGTCCGCGACAGCAGGTAAGTGAGGCTCAGAAGCCGGCG A C EXD2 Ensembl:ENSG00000081177 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69191567..69191675 26863196 MeRIP-seq:(Medium) rs944448205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1529727,Human_Splice_Rec_1529743,Human_Splice_Rec_1529761,Human_Splice_Rec_1529781,Human_Splice_Rec_1529787 72057 RMVar_ID_72057 Human_SNP_ID_559478083 m1A Human chr14 + 69237930 69237929 69237930 AGATGCTTCAAGAGGCTGCCAGCCTGGAGACCAGGTACAAAGCACAGGAATTGTGGAATGTACCA AGATGCTTCAAGAGGCTGCCAGCCTGGAGACC_GGTACAAAGCACAGGAATTGTGGAATGTACCA CA C EXD2 Ensembl:ENSG00000081177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:69237886..69240939 32194978 MeRIP-seq:(Medium) rs1268952125 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1529741,Human_Splice_Rec_1529759,Human_Splice_Rec_1529779,Human_Splice_Rec_1529799,Human_Splice_Rec_1529817,Human_Splice_Rec_1529833,Human_Splice_Rec_1529849 RMVar_hsa_circ_90172,RMVar_hsa_circ_335843,RMVar_hsa_circ_167508,RMVar_hsa_circ_167507 72058 RMVar_ID_72058 Human_SNP_ID_559478084 m1A Human chr14 + 69237930 69237930 69237930 AGATGCTTCAAGAGGCTGCCAGCCTGGAGACCAGGTACAAAGCACAGGAATTGTGGAATGTACCA AGATGCTTCAAGAGGCTGCCAGCCTGGAGACCGGGTACAAAGCACAGGAATTGTGGAATGTACCA A G EXD2 Ensembl:ENSG00000081177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:69237886..69240939 32194978 MeRIP-seq:(Medium) rs1261111662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1529741,Human_Splice_Rec_1529759,Human_Splice_Rec_1529779,Human_Splice_Rec_1529799,Human_Splice_Rec_1529817,Human_Splice_Rec_1529833,Human_Splice_Rec_1529849 RMVar_hsa_circ_90172,RMVar_hsa_circ_335843,RMVar_hsa_circ_167508,RMVar_hsa_circ_167507 72059 RMVar_ID_72059 Human_SNP_ID_559505031 m1A Human chr14 + 69352687 69352687 69352687 TGCAGGGGTAGCTGAAGAACAGGAAGGAGGTGAGAAGCCCGGTGACCTGTCAGAGATGCCAAGCC TGCAGGGGTAGCTGAAGAACAGGAAGGAGGTGTGAAGCCCGGTGACCTGTCAGAGATGCCAAGCC A T GALNT16 Ensembl:ENSG00000100626 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69352637..69352744 26863196 MeRIP-seq:(Medium) rs948638883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266963 72060 RMVar_ID_72060 Human_SNP_ID_559512323 m1A Human chr14 - 69384903 69384903 69384903 GGCCAAGAGAGGGTAGGAGATGAGATCATTAGAGGAAAAGACTTCATGGAATTGGGAGGCCTAAG GGCCAAGAGAGGGTAGGAGATGAGATCATTAGGGGAAAAGACTTCATGGAATTGGGAGGCCTAAG T C ERH Ensembl:ENSG00000100632 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69384900..69384994 26863196 MeRIP-seq:(Medium) rs1391681014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12398820 RMVar_hsa_circ_98800,RMVar_hsa_circ_122006,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167515,RMVar_hsa_circ_167514 72061 RMVar_ID_72061 Human_SNP_ID_559514841 m1A Human chr14 - 69394831 69394831 69394831 CTTATGCTGACTACGAATCTGTGAATGAATGCATGGAAGGTGAGTTTAACACTAATCAAGGGGTA CTTATGCTGACTACGAATCTGTGAATGAATGCGTGGAAGGTGAGTTTAACACTAATCAAGGGGTA T C ERH Ensembl:ENSG00000100632 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69394826..69394850 26863196 MeRIP-seq:(Medium) rs1487322787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450547,Human_RBP_ID_1497944,Human_RBP_ID_6376662,Human_RBP_ID_23633334 Human_Splice_Rec_1530026,Human_Splice_Rec_1530027,Human_Splice_Rec_1530035,Human_Splice_Rec_1530038,Human_Splice_Rec_1530039 Human_miRNA_ID_2896891 RMVar_hsa_circ_98800,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167514,RMVar_hsa_circ_325472 72062 RMVar_ID_72062 Human_SNP_ID_559514856 m1A Human chr14 + 69394910 69394910 69394910 CTCTTGGTAGGCTGTACCAGCAAAATGGTGTGAGACTGCAGGGGAAAACATGATTTCAATATAAG CTCTTGGTAGGCTGTACCAGCAAAATGGTGTGGGACTGCAGGGGAAAACATGATTTCAATATAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:69386976..69398364 32194978 MeRIP-seq:(Medium) rs1426728690 Functional Loss SNV dbSNP153 33..33 33 - - - 72063 RMVar_ID_72063 Human_SNP_ID_559515730 m1A Human chr14 + 69398159 69398159 69398159 ACGCGGCGCTGCATGGGGCTCGTGGGGAGGGGAAAACGTATGGGGCTGGGGTCGCTCTGGAGGCC ACGCGGCGCTGCATGGGGCTCGTGGGGAGGGGGAAACGTATGGGGCTGGGGTCGCTCTGGAGGCC A G SLC39A9 Ensembl:ENSG00000029364 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:69398157..69398300 26863196 MeRIP-seq:(Medium) rs1304289320 Functional Loss SNV dbSNP153 33..33 33 - - - 72064 RMVar_ID_72064 Human_SNP_ID_559515986 m1A Human chr14 + 69398797 69398797 69398797 ACCATGGGCAGCACCGGGTATAGGGCAGAGACAGCTTTGTGTCAACTTTGCTGCTGAACCCCTAG ACCATGGGCAGCACCGGGTATAGGGCAGAGACGGCTTTGTGTCAACTTTGCTGCTGAACCCCTAG A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:69398747..69398842 26863196 MeRIP-seq:(Medium) rs554448602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1362116,Human_RBP_ID_4308393 Human_miRNA_ID_894609,Human_miRNA_ID_901273,Human_miRNA_ID_907921,Human_miRNA_ID_914561,Human_miRNA_ID_1238754 72065 RMVar_ID_72065 Human_SNP_ID_559530343 m1A Human chr14 + 69458446 69458446 69458446 TTCTCTGCCGGGACATTTCTTTATGTTGCCACAGTACATGTCCTCCCTGAGGTGGGCGGAATAGG TTCTCTGCCGGGACATTTCTTTATGTTGCCACGGTACATGTCCTCCCTGAGGTGGGCGGAATAGG A G SLC39A9 Ensembl:ENSG00000029364 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:69454816..69458446 32194978 MeRIP-seq:(Medium) rs770206308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450575,Human_RBP_ID_880999,Human_RBP_ID_21887131,Human_RBP_ID_22757908 Human_Splice_Rec_1530060,Human_Splice_Rec_1530074,Human_Splice_Rec_1530100,Human_Splice_Rec_1530110,Human_Splice_Rec_1530122,Human_Splice_Rec_1530138,Human_Splice_Rec_1530150,Human_Splice_Rec_1530154 Human_miRNA_ID_2029845,Human_miRNA_ID_2029846,Human_miRNA_ID_2690324,Human_miRNA_ID_2690325,Human_miRNA_ID_2693601,Human_miRNA_ID_2693602 RMVar_hsa_circ_78832,RMVar_hsa_circ_84384,RMVar_hsa_circ_167518,RMVar_hsa_circ_167522,RMVar_hsa_circ_37026,RMVar_hsa_circ_290201,RMVar_hsa_circ_167529,RMVar_hsa_circ_167531,RMVar_hsa_circ_94098 72066 RMVar_ID_72066 Human_SNP_ID_559603291 m1A Human chr14 - 69767173 69767173 69767173 CGACGGAGTCGTCGACCTCCACGCAGACCAGGACTTAACTCGTCTACGCCACTCCACAACTGACG CGACGGAGTCGTCGACCTCCACGCAGACCAGGGCTTAACTCGTCTACGCCACTCCACAACTGACG T C LOC100289511 RNACentral:URS000075CEC0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:69767101..69767463;chr14:69767101..69767447 26863196 MeRIP-seq:(Medium) rs1419142690 Functional Loss SNV dbSNP153 33..33 33 - - - 72067 RMVar_ID_72067 Human_SNP_ID_559603341 m1A Human chr14 - 69767286 69767286 69767286 GATCTGAGCGGCCATGAAGAAGCCTCGATCCGAGAAGGCTTGCCCTCAAAGTGAGCCACTCACCT GATCTGAGCGGCCATGAAGAAGCCTCGATCCGGGAAGGCTTGCCCTCAAAGTGAGCCACTCACCT T C LOC100289511 RNACentral:URS000075CEC0 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69767276..69767675 32194978 MeRIP-seq:(Medium) rs1346228443 Functional Loss SNV dbSNP153 33..33 33 - - - 72068 RMVar_ID_72068 Human_SNP_ID_559603628 m1A Human chr14 - 69767707 69767703 69767707 CGCGACGCCTCGACCGCGCCTGCGCCAACAGCAGCGGGCGGGCGCTCTGCGGCCACAAAATGGCG CGCGACGCCTCGACCGCGCCTGCGCCAACAGC____GGCGGGCGCTCTGCGGCCACAAAATGGCG CCGCT C LOC100289511 RNACentral:URS000075CEC0 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69767701..69768000 32194978 MeRIP-seq:(Medium) rs1566624387 Functional Loss DEL dbSNP153 33..36 33 - - - 72069 RMVar_ID_72069 Human_SNP_ID_559603637 m1A Human chr14 - 69767707 69767707 69767707 CGCGACGCCTCGACCGCGCCTGCGCCAACAGCAGCGGGCGGGCGCTCTGCGGCCACAAAATGGCG CGCGACGCCTCGACCGCGCCTGCGCCAACAGCTGCGGGCGGGCGCTCTGCGGCCACAAAATGGCG T A LOC100289511 RNACentral:URS000075CEC0 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69767701..69768000 32194978 MeRIP-seq:(Medium) rs931242758 Functional Loss SNV dbSNP153 33..33 33 - - - 72070 RMVar_ID_72070 Human_SNP_ID_559603638 m1A Human chr14 - 69767707 69767707 69767707 CGCGACGCCTCGACCGCGCCTGCGCCAACAGCAGCGGGCGGGCGCTCTGCGGCCACAAAATGGCG CGCGACGCCTCGACCGCGCCTGCGCCAACAGCCGCGGGCGGGCGCTCTGCGGCCACAAAATGGCG T G LOC100289511 RNACentral:URS000075CEC0 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:69767701..69768000 32194978 MeRIP-seq:(Medium) rs931242758 Functional Loss SNV dbSNP153 33..33 33 - - - 72071 RMVar_ID_72071 Human_SNP_ID_559603871 m1A Human chr14 + 69768251 69768251 69768251 AAGATTCTTCAAGGGATATGGACGGATAAGAGATATTGATCTGAAAAGAGGCTTTGGTTTTGTGG AAGATTCTTCAAGGGATATGGACGGATAAGAGGTATTGATCTGAAAAGAGGCTTTGGTTTTGTGG A G SRSF5 Ensembl:ENSG00000100650 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:69768114..69768302 26863196 MeRIP-seq:(Medium) rs1329768425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39268,Human_RBP_ID_231026,Human_RBP_ID_1498037,Human_RBP_ID_1823359,Human_RBP_ID_4313984,Human_RBP_ID_5563386,Human_RBP_ID_6377113,Human_RBP_ID_9044412,Human_RBP_ID_9369135,Human_RBP_ID_12399929,Human_RBP_ID_18436019,Human_RBP_ID_22926225,Human_RBP_ID_23118236,Human_RBP_ID_23633521,Human_RBP_ID_26325188,Human_RBP_ID_26627780,Human_RBP_ID_27808390 Human_Splice_Rec_1530205,Human_Splice_Rec_1530219,Human_Splice_Rec_1530233,Human_Splice_Rec_1530243,Human_Splice_Rec_1530251,Human_Splice_Rec_1530263,Human_Splice_Rec_1530277,Human_Splice_Rec_1530291,Human_Splice_Rec_1530303,Human_Splice_Rec_1530313,Human_Splice_Rec_1530325,Human_Splice_Rec_1530339,Human_Splice_Rec_1530341,Human_Splice_Rec_1530345,Human_Splice_Rec_1530353 RMVar_hsa_circ_60300,RMVar_hsa_circ_167537,RMVar_hsa_circ_76152,RMVar_hsa_circ_344460,RMVar_hsa_circ_365571,RMVar_hsa_circ_328171,RMVar_hsa_circ_53304 72072 RMVar_ID_72072 Human_SNP_ID_559603872 m1A Human chr14 - 69768252 69768252 69768252 ACCACAAAACCAAAGCCTCTTTTCAGATCAATATCTCTTATCCGTCCATATCCCTTGAAGAATCT ACCACAAAACCAAAGCCTCTTTTCAGATCAATCTCTCTTATCCGTCCATATCCCTTGAAGAATCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69768098..69768321 26863196 MeRIP-seq:(Medium) rs777232426 Functional Loss SNV dbSNP153 33..33 33 - - - 72073 RMVar_ID_72073 Human_SNP_ID_559604097 m1A Human chr14 + 69768846 69768846 69768846 GCTAGGGCTCGGTCACGAGGTGGAAGAGGTAGAGGACGATACTCTGACCGTTTTAGTAGTCGCAG GCTAGGGCTCGGTCACGAGGTGGAAGAGGTAGGGGACGATACTCTGACCGTTTTAGTAGTCGCAG A G SRSF5 Ensembl:ENSG00000100650 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:69768776..69769001 32194978 MeRIP-seq:(Medium) rs1022203283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39271,Human_RBP_ID_231028,Human_RBP_ID_450714,Human_RBP_ID_813237,Human_RBP_ID_882736,Human_RBP_ID_1823364,Human_RBP_ID_5563389,Human_RBP_ID_6377121,Human_RBP_ID_12399957,Human_RBP_ID_18655166,Human_RBP_ID_23633531,Human_RBP_ID_26326276,Human_RBP_ID_27647152 Human_Splice_Rec_1530208,Human_Splice_Rec_1530209,Human_Splice_Rec_1530222,Human_Splice_Rec_1530223,Human_Splice_Rec_1530236,Human_Splice_Rec_1530246,Human_Splice_Rec_1530247,Human_Splice_Rec_1530254,Human_Splice_Rec_1530255,Human_Splice_Rec_1530266,Human_Splice_Rec_1530267,Human_Splice_Rec_1530280,Human_Splice_Rec_1530281,Human_Splice_Rec_1530294,Human_Splice_Rec_1530295,Human_Splice_Rec_1530306,Human_Splice_Rec_1530316,Human_Splice_Rec_1530328,Human_Splice_Rec_1530329,Human_Splice_Rec_1530348,Human_Splice_Rec_1530349,Human_Splice_Rec_1530356,Human_Splice_Rec_1530357 Human_miRNA_ID_2571006,Human_miRNA_ID_3044743 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152,RMVar_hsa_circ_365571,RMVar_hsa_circ_328171,RMVar_hsa_circ_56344,RMVar_hsa_circ_53304,RMVar_hsa_circ_20077 72074 RMVar_ID_72074 Human_SNP_ID_559604098 m1A Human chr14 + 69768849 69768849 69768849 AGGGCTCGGTCACGAGGTGGAAGAGGTAGAGGACGATACTCTGACCGTTTTAGTAGTCGCAGACC AGGGCTCGGTCACGAGGTGGAAGAGGTAGAGGGCGATACTCTGACCGTTTTAGTAGTCGCAGACC A G SRSF5 Ensembl:ENSG00000100650 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:69768771..69768903;chr14:69768776..69768925;chr14:69768776..69768902 26863196 MeRIP-seq:(Medium) rs1211287735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39271,Human_RBP_ID_231028,Human_RBP_ID_450714,Human_RBP_ID_813237,Human_RBP_ID_882736,Human_RBP_ID_1823364,Human_RBP_ID_5563389,Human_RBP_ID_6377121,Human_RBP_ID_12399957,Human_RBP_ID_18655166,Human_RBP_ID_22188154,Human_RBP_ID_23633531,Human_RBP_ID_26326276 Human_Splice_Rec_1530208,Human_Splice_Rec_1530209,Human_Splice_Rec_1530222,Human_Splice_Rec_1530223,Human_Splice_Rec_1530236,Human_Splice_Rec_1530246,Human_Splice_Rec_1530247,Human_Splice_Rec_1530254,Human_Splice_Rec_1530255,Human_Splice_Rec_1530266,Human_Splice_Rec_1530267,Human_Splice_Rec_1530280,Human_Splice_Rec_1530281,Human_Splice_Rec_1530294,Human_Splice_Rec_1530295,Human_Splice_Rec_1530306,Human_Splice_Rec_1530316,Human_Splice_Rec_1530328,Human_Splice_Rec_1530329,Human_Splice_Rec_1530348,Human_Splice_Rec_1530349,Human_Splice_Rec_1530356,Human_Splice_Rec_1530357 Human_miRNA_ID_2571006,Human_miRNA_ID_3044743 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152,RMVar_hsa_circ_365571,RMVar_hsa_circ_328171,RMVar_hsa_circ_56344,RMVar_hsa_circ_53304,RMVar_hsa_circ_20077 72075 RMVar_ID_72075 Human_SNP_ID_559604134 m1A Human chr14 + 69768931 69768931 69768931 ATGTGAAGGGTGGATGGCTGCATTGAACAATTATTGTAGGGGTAGCATTTAAGATTCAGGAGTCA ATGTGAAGGGTGGATGGCTGCATTGAACAATTGTTGTAGGGGTAGCATTTAAGATTCAGGAGTCA A G SRSF5 Ensembl:ENSG00000100650 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:69768771..69768975 26863196 MeRIP-seq:(Medium) rs993299508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39272,Human_RBP_ID_813238,Human_RBP_ID_1498053,Human_RBP_ID_1823365,Human_RBP_ID_5351744,Human_RBP_ID_12399960,Human_RBP_ID_17604047,Human_RBP_ID_19064156,Human_RBP_ID_22649146,Human_RBP_ID_23633535,Human_RBP_ID_26778075 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152,RMVar_hsa_circ_328171,RMVar_hsa_circ_53304,RMVar_hsa_circ_20077 72076 RMVar_ID_72076 Human_SNP_ID_559604446 m1A Human chr14 + 69769882 69769882 69769882 AACTGCTCGAGTAGAACATGTCTGCATCCGCCAATAGTCCGCTAATAGGGAGGGCTGTGCGATTA AACTGCTCGAGTAGAACATGTCTGCATCCGCCGATAGTCCGCTAATAGGGAGGGCTGTGCGATTA A G SRSF5 Ensembl:ENSG00000100650 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:69769831..69769981 26863196 MeRIP-seq:(Medium) rs1165222366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450734,Human_RBP_ID_1498075,Human_RBP_ID_3459064,Human_RBP_ID_6377155,Human_RBP_ID_9044427,Human_RBP_ID_12400001,Human_RBP_ID_18655187,Human_RBP_ID_22798201 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152,RMVar_hsa_circ_111225,RMVar_hsa_circ_53304,RMVar_hsa_circ_167538 72077 RMVar_ID_72077 Human_SNP_ID_559605084 m1A Human chr14 + 69771495 69771495 69771495 CTGTAAATAACTTGCCCTGGGGGCCTTTTTTTAAAAAACAAAAACCACAAAAATTCCCAAACCAT CTGTAAATAACTTGCCCTGGGGGCCTTTTTTTCAAAAACAAAAACCACAAAAATTCCCAAACCAT A C SRSF5 Ensembl:ENSG00000100650 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs777779615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39290,Human_RBP_ID_450757,Human_RBP_ID_1498118,Human_RBP_ID_1823399,Human_RBP_ID_2424149,Human_RBP_ID_3459078,Human_RBP_ID_8250269,Human_RBP_ID_8408560,Human_RBP_ID_9044444,Human_RBP_ID_17247782,Human_RBP_ID_18161422,Human_RBP_ID_18655216,Human_RBP_ID_21886796,Human_RBP_ID_22043915,Human_RBP_ID_22188188,Human_RBP_ID_22798230,Human_RBP_ID_24472154,Human_RBP_ID_25110651,Human_RBP_ID_26627794,Human_RBP_ID_26927208,Human_RBP_ID_27228309,Human_RBP_ID_27432513 Human_Splice_Rec_1530371 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152 72078 RMVar_ID_72078 Human_SNP_ID_559605085 m1A Human chr14 + 69771495 69771495 69771495 CTGTAAATAACTTGCCCTGGGGGCCTTTTTTTAAAAAACAAAAACCACAAAAATTCCCAAACCAT CTGTAAATAACTTGCCCTGGGGGCCTTTTTTTGAAAAACAAAAACCACAAAAATTCCCAAACCAT A G SRSF5 Ensembl:ENSG00000100650 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs777779615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39290,Human_RBP_ID_450757,Human_RBP_ID_1498118,Human_RBP_ID_1823399,Human_RBP_ID_2424149,Human_RBP_ID_3459078,Human_RBP_ID_8250269,Human_RBP_ID_8408560,Human_RBP_ID_9044444,Human_RBP_ID_17247782,Human_RBP_ID_18161422,Human_RBP_ID_18655216,Human_RBP_ID_21886796,Human_RBP_ID_22043915,Human_RBP_ID_22188188,Human_RBP_ID_22798230,Human_RBP_ID_24472154,Human_RBP_ID_25110651,Human_RBP_ID_26627794,Human_RBP_ID_26927208,Human_RBP_ID_27228309,Human_RBP_ID_27432513 Human_Splice_Rec_1530371 RMVar_hsa_circ_167537,RMVar_hsa_circ_76152 72079 RMVar_ID_72079 Human_SNP_ID_559632562 m1A Human chr14 - 69879539 69879539 69879539 GAGCGGGCCGTGGTCCTGCGGCGGGGGCTCGCAGAGGCTGCGGTCAGGGGACACAGTCATGAACC GAGCGGGCCGTGGTCCTGCGGCGGGGGCTCGCGGAGGCTGCGGTCAGGGGACACAGTCATGAACC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:69879426..69879646 26863196 MeRIP-seq:(Medium) rs1443342992 Functional Loss SNV dbSNP153 33..33 33 - - - 72080 RMVar_ID_72080 Human_SNP_ID_559633935 m1A Human chr14 - 69885281 69885281 69885281 TAAAAATAATTAAAATAATACAAATTTTCCTTAAAAAAAAAAAAAAAGAAGTTGTTCGAAGGAGA TAAAAATAATTAAAATAATACAAATTTTCCTTCAAAAAAAAAAAAAAGAAGTTGTTCGAAGGAGA T G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879218476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450776,Human_RBP_ID_26430230 72081 RMVar_ID_72081 Human_SNP_ID_559649681 m1A Human chr14 + 69953372 69953372 69953372 TGGTTTTCTCAGCCATTTTGTCCCTCGGCCCCAGTGTCGAATCCAAGTGAAATATGAAATCTGCT TGGTTTTCTCAGCCATTTTGTCCCTCGGCCCCTGTGTCGAATCCAAGTGAAATATGAAATCTGCT A T SMOC1 Ensembl:ENSG00000198732 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:69953369..69953571 26863196 MeRIP-seq:(Medium) rs1243480946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21,RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_319759,RMVar_hsa_circ_35200,RMVar_hsa_circ_167541 72082 RMVar_ID_72082 Human_SNP_ID_559654365 m1A Human chr14 + 69974186 69974185 69974186 TAGCATGCAGTCCCTGAGGTCACGATCTTGAGAGGGGGGAGTGGACTGGATGAATCAACAGCTAG TAGCATGCAGTCCCTGAGGTCACGATCTTGAG_GGGGGGAGTGGACTGGATGAATCAACAGCTAG GA G SMOC1 Ensembl:ENSG00000198732 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69974184..69974618 26863196 MeRIP-seq:(Medium) rs1390447724 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_35200 72083 RMVar_ID_72083 Human_SNP_ID_559655900 m1A Human chr14 + 69980804 69980804 69980804 TGCAAAGAGGTGCTGGGTCTGCACCCTTGTGCAGGGTGATGGATATGGCCAGAAAAGAGGTGGGG TGCAAAGAGGTGCTGGGTCTGCACCCTTGTGCGGGGTGATGGATATGGCCAGAAAAGAGGTGGGG A G SMOC1 Ensembl:ENSG00000198732 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69980803..69981223 26863196 MeRIP-seq:(Medium) rs74060663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6377779 RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_278946,RMVar_hsa_circ_291619,RMVar_hsa_circ_293800,RMVar_hsa_circ_113137,RMVar_hsa_circ_167544,RMVar_hsa_circ_167546,RMVar_hsa_circ_167545,RMVar_hsa_circ_167543,RMVar_hsa_circ_167549,RMVar_hsa_circ_89645,RMVar_hsa_circ_167548 72084 RMVar_ID_72084 Human_SNP_ID_559655904 m1A Human chr14 + 69980822 69980822 69980822 CTGCACCCTTGTGCAGGGTGATGGATATGGCCAGAAAAGAGGTGGGGCCAGAGGTCTGGAGGTGT CTGCACCCTTGTGCAGGGTGATGGATATGGCCCGAAAAGAGGTGGGGCCAGAGGTCTGGAGGTGT A C SMOC1 Ensembl:ENSG00000198732 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:69980817..69981202 26863196 MeRIP-seq:(Medium) rs375978278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_278946,RMVar_hsa_circ_291619,RMVar_hsa_circ_293800,RMVar_hsa_circ_113137,RMVar_hsa_circ_167544,RMVar_hsa_circ_167546,RMVar_hsa_circ_167545,RMVar_hsa_circ_167543,RMVar_hsa_circ_167549,RMVar_hsa_circ_89645,RMVar_hsa_circ_167548 72085 RMVar_ID_72085 Human_SNP_ID_559658647 m1A Human chr14 - 69993003 69993003 69993003 TCAAGTCCTGGCTCTTCACAAAAGCTTTTCCCAGACCATGGTGATCTCTTTCTTCCATAAATGTC TCAAGTCCTGGCTCTTCACAAAAGCTTTTCCCCGACCATGGTGATCTCTTTCTTCCATAAATGTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:69993002..69993304 26863196 MeRIP-seq:(Medium) rs181122998 Functional Loss SNV dbSNP153 33..33 33 - - - 72086 RMVar_ID_72086 Human_SNP_ID_559662903 m1A Human chr14 + 70011559 70011559 70011559 TACAGAGGCGGATGACCCCTTCAAGGACAGGGAGCTACCAGGTGGGAGACGATGCTGCCCTGCCG TACAGAGGCGGATGACCCCTTCAAGGACAGGGTGCTACCAGGTGGGAGACGATGCTGCCCTGCCG A T SMOC1 Ensembl:ENSG00000198732 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:70011465..70011612 26863196 MeRIP-seq:(Medium) rs142050630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22758163 Human_Splice_Rec_1530404,Human_Splice_Rec_1530405,Human_Splice_Rec_1530426,Human_Splice_Rec_1530427,Human_Splice_Rec_1530442 Human_miRNA_ID_2444236 RMVar_hsa_circ_78270,RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_278946,RMVar_hsa_circ_291619,RMVar_hsa_circ_113137,RMVar_hsa_circ_167544,RMVar_hsa_circ_167543,RMVar_hsa_circ_167549,RMVar_hsa_circ_89645,RMVar_hsa_circ_167550,RMVar_hsa_circ_167548,RMVar_hsa_circ_323721,RMVar_hsa_circ_333915,RMVar_hsa_circ_95898,RMVar_hsa_circ_167552,RMVar_hsa_circ_167554,RMVar_hsa_circ_167553,RMVar_hsa_circ_167555,RMVar_hsa_circ_79835,RMVar_hsa_circ_167556,RMVar_hsa_circ_280496,RMVar_hsa_circ_354555,RMVar_hsa_circ_167557 72087 RMVar_ID_72087 Human_SNP_ID_559665889 m1A Human chr14 - 70024981 70024981 70024981 CTAACTTGATCTCCAATCACCCACTTCTCTCCATTCCCCTTACCCTGCTGTGTTTTCATAACTTG CTAACTTGATCTCCAATCACCCACTTCTCTCCTTTCCCCTTACCCTGCTGTGTTTTCATAACTTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:70024978..70025152 26863196 MeRIP-seq:(Medium) rs1332864972 Functional Loss SNV dbSNP153 33..33 33 - - - 72088 RMVar_ID_72088 Human_SNP_ID_559746073 m1A Human chr14 - 70345906 70345906 70345906 CTGGGAAGATGGCAGCTGAGAAGACAACGAGGAGGCTTGGGGGGTTAAAAAAGATGGTTGAGAGG CTGGGAAGATGGCAGCTGAGAAGACAACGAGGCGGCTTGGGGGGTTAAAAAAGATGGTTGAGAGG T G SYNJ2BP-COX16,COX16 Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70345904..70346027 26863196 MeRIP-seq:(Medium) rs1285946731 Functional Loss SNV dbSNP153 33..33 33 - - - 72089 RMVar_ID_72089 Human_SNP_ID_559746076 m1A Human chr14 + 70345929 70345914 70345929 CCCCAAGCCTCCTCGTTGTCTTCTCAGCTGCCATCTTCCCAGCTGCCATCTTCCCAGTCAGCTGT CCCCAAGCCTCCTCGTTG_______________TCTTCCCAGCTGCCATCTTCCCAGTCAGCTGT GTCTTCTCAGCTGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:70345927..70346055 26863196 MeRIP-seq:(Medium) rs1024287689 Functional Loss DEL dbSNP153 19..33 33 - - - 72090 RMVar_ID_72090 Human_SNP_ID_559746083 m1A Human chr14 + 70345929 70345929 70345929 CCCCAAGCCTCCTCGTTGTCTTCTCAGCTGCCATCTTCCCAGCTGCCATCTTCCCAGTCAGCTGT CCCCAAGCCTCCTCGTTGTCTTCTCAGCTGCCCTCTTCCCAGCTGCCATCTTCCCAGTCAGCTGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:70345927..70346055 26863196 MeRIP-seq:(Medium) rs143046241 Functional Loss SNV dbSNP153 33..33 33 - - - 72091 RMVar_ID_72091 Human_SNP_ID_559746332 m1A Human chr14 - 70346916 70346916 70346916 CCCGAGGGGTCTGGGTTGATGCGTTGGGTACTATGGGGAATGTGCAAGTGGAGAGTAGTGTGGAG CCCGAGGGGTCTGGGTTGATGCGTTGGGTACTTTGGGGAATGTGCAAGTGGAGAGTAGTGTGGAG T A SYNJ2BP-COX16,COX16 Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70346909..70347003 26863196 MeRIP-seq:(Medium) rs1472845774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23633805 72092 RMVar_ID_72092 Human_SNP_ID_559746333 m1A Human chr14 - 70346916 70346916 70346916 CCCGAGGGGTCTGGGTTGATGCGTTGGGTACTATGGGGAATGTGCAAGTGGAGAGTAGTGTGGAG CCCGAGGGGTCTGGGTTGATGCGTTGGGTACTGTGGGGAATGTGCAAGTGGAGAGTAGTGTGGAG T C SYNJ2BP-COX16,COX16 Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70346909..70347003 26863196 MeRIP-seq:(Medium) rs1472845774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23633805 72093 RMVar_ID_72093 Human_SNP_ID_559806938 m1A Human chr14 - 70597774 70597774 70597774 CCTTTATCATTTTGTTTTCTTTCCCATAGACAATCTGCTGGGAATTTCTTGGGTTGACAGCTCTT CCTTTATCATTTTGTTTTCTTTCCCATAGACAGTCTGCTGGGAATTTCTTGGGTTGACAGCTCTT T C MED6,AL357153.3 Ensembl:ENSG00000133997,Ensembl:ENSG00000259115 Protein coding,lincRNA CDS,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:70597695..70633773 26863196 MeRIP-seq:(Medium) rs1391126534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4309406 Human_Splice_Rec_1530664,Human_Splice_Rec_1530680,Human_Splice_Rec_1530696,Human_Splice_Rec_1530710,Human_Splice_Rec_1530724,Human_Splice_Rec_1530740,Human_Splice_Rec_1530750,Human_Splice_Rec_1530760,Human_Splice_Rec_1530768,Human_Splice_Rec_1530776,Human_Splice_Rec_1530782 Human_miRNA_ID_3163782,Human_miRNA_ID_3191264,Human_miRNA_ID_3209986 RMVar_hsa_circ_317306,RMVar_hsa_circ_167569,RMVar_hsa_circ_72426,RMVar_hsa_circ_167570,RMVar_hsa_circ_276353,RMVar_hsa_circ_3362,RMVar_hsa_circ_167572,RMVar_hsa_circ_167574 72094 RMVar_ID_72094 Human_SNP_ID_559817717 m1A Human chr14 + 70642136 70642136 70642136 GCACCAGGCGCCGGGGCGGCGGCCGAATGGAGAGAAAGGGCTCGGCGGCCGGGGCCAAGGGGAAC GCACCAGGCGCCGGGGCGGCGGCCGAATGGAGGGAAAGGGCTCGGCGGCCGGGGCCAAGGGGAAC A G TTC9 Ensembl:ENSG00000133985 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:70641793..70642532 26863196 MeRIP-seq:(Medium) rs1265113760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4300331 72095 RMVar_ID_72095 Human_SNP_ID_559817880 m1A Human chr14 - 70642430 70642430 70642430 CTTCAGGGCCCCAGCCGGGGAGGCCGGGCGCGAGTCCCGCTCCCGTTCCCCGGGGGGCGGCAGCA CTTCAGGGCCCCAGCCGGGGAGGCCGGGCGCGGGTCCCGCTCCCGTTCCCCGGGGGGCGGCAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:70642382..70667709 32194978 MeRIP-seq:(Medium) rs1405383069 Functional Loss SNV dbSNP153 33..33 33 - - - 72096 RMVar_ID_72096 Human_SNP_ID_559824512 m1A Human chr14 + 70671162 70671162 70671162 CCCAGAGAGAAAAAGAAGCCATGTAACCAGGAAGCAGCTCCAGAGCTGCGCCCACGCCTGACCGG CCCAGAGAGAAAAAGAAGCCATGTAACCAGGAGGCAGCTCCAGAGCTGCGCCCACGCCTGACCGG A G TTC9 Ensembl:ENSG00000133985 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:70671112..70671286 26863196 MeRIP-seq:(Medium) rs759348074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1530794 RMVar_hsa_circ_167575 72097 RMVar_ID_72097 Human_SNP_ID_559824741 m1A Human chr14 + 70671999 70671999 70671999 ATAGGCTAGGGGATTGAACTGTGGACTGATTCAGTGTAAATAAAAACAAATTAACAGGTAGTAGT ATAGGCTAGGGGATTGAACTGTGGACTGATTCCGTGTAAATAAAAACAAATTAACAGGTAGTAGT A C TTC9 Ensembl:ENSG00000133985 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA Glucose starvation 4h chr14:70671949..70672035 31548705,26863196 m1A-quant-seq:(High) rs1076265 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8774,GWAS_ID_8775,GWAS_ID_8776 RMVar_hsa_circ_167575 72098 RMVar_ID_72098 Human_SNP_ID_559824742 m1A Human chr14 + 70671999 70671999 70671999 ATAGGCTAGGGGATTGAACTGTGGACTGATTCAGTGTAAATAAAAACAAATTAACAGGTAGTAGT ATAGGCTAGGGGATTGAACTGTGGACTGATTCTGTGTAAATAAAAACAAATTAACAGGTAGTAGT A T TTC9 Ensembl:ENSG00000133985 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA Glucose starvation 4h chr14:70671949..70672035 31548705,26863196 m1A-quant-seq:(High) rs1076265 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8774,GWAS_ID_8775,GWAS_ID_8776 RMVar_hsa_circ_167575 72099 RMVar_ID_72099 Human_SNP_ID_559839088 m1A Human chr14 + 70732744 70732744 70732744 TCTACTCGGACATTGACCAGGGGGTTGTGGGTACATGGACTCAGGGGAGGGGCCTCGACTGGGCT TCTACTCGGACATTGACCAGGGGGTTGTGGGTGCATGGACTCAGGGGAGGGGCCTCGACTGGGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:70732693..70732810 26863196 MeRIP-seq:(Medium) rs1178312186 Functional Loss SNV dbSNP153 33..33 33 - - - 72100 RMVar_ID_72100 Human_SNP_ID_559839200 m1A Human chr14 - 70732985 70732985 70732985 GCCACCAGCCCGGGAGGAGAAGAAAAGACGGGAGGGTCTTTTTCAGAGGTCCAGCCGTCCTCGTC GCCACCAGCCCGGGAGGAGAAGAAAAGACGGGGGGGTCTTTTTCAGAGGTCCAGCCGTCCTCGTC T C MAP3K9 Ensembl:ENSG00000006432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:70732938..70733139 32194978 MeRIP-seq:(Medium) rs1156877131 Functional Loss SNV dbSNP153 33..33 33 - - - 72101 RMVar_ID_72101 Human_SNP_ID_559857475 m1A Human chr14 + 70808954 70808954 70808954 TGGACAGCACCTCCACCACGTCGCCCAGCCGCAGGGTCAGCTCGTCCTCGCCCGCCGCCTCGTAC TGGACAGCACCTCCACCACGTCGCCCAGCCGCGGGGTCAGCTCGTCCTCGCCCGCCGCCTCGTAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:70808846..70809038 26863196 MeRIP-seq:(Medium) rs750161590 Functional Loss SNV dbSNP153 33..33 33 - - - 72102 RMVar_ID_72102 Human_SNP_ID_559857476 m1A Human chr14 + 70808954 70808954 70808954 TGGACAGCACCTCCACCACGTCGCCCAGCCGCAGGGTCAGCTCGTCCTCGCCCGCCGCCTCGTAC TGGACAGCACCTCCACCACGTCGCCCAGCCGCTGGGTCAGCTCGTCCTCGCCCGCCGCCTCGTAC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:70808846..70809038 26863196 MeRIP-seq:(Medium) rs750161590 Functional Loss SNV dbSNP153 33..33 33 - - - 72103 RMVar_ID_72103 Human_SNP_ID_559857675 m1A Human chr14 + 70809353 70809353 70809353 GCTCGCCGGCGCTGTTACCGCGGTACGAGAAGAGCGCCGAGCGCGAGCTCTTCGCGCAGCCTAGG GCTCGCCGGCGCTGTTACCGCGGTACGAGAAGGGCGCCGAGCGCGAGCTCTTCGCGCAGCCTAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70809313..70809531 26863196 MeRIP-seq:(Medium) rs1344741362 Functional Loss SNV dbSNP153 33..33 33 - - - 72104 RMVar_ID_72104 Human_SNP_ID_559860630 m1A Human chr14 - 70822059 70822042 70822059 GACGCCACGGCCCCGAAGCCGCGAGTGACCGCAGCTCCGATCCCCCGGCGGGAGGCCTGCCCGAG GACGCCACGGCCCCGAAGCCGCGAGTGACCGC_________________GGGAGGCCTGCCCGAG CGCCGGGGGATCGGAGCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:70822008..70822121 26863196 MeRIP-seq:(Medium) rs1435486888 Functional Loss DEL dbSNP153 33..49 33 - - - 72105 RMVar_ID_72105 Human_SNP_ID_559860635 m1A Human chr14 - 70822059 70822059 70822059 GACGCCACGGCCCCGAAGCCGCGAGTGACCGCAGCTCCGATCCCCCGGCGGGAGGCCTGCCCGAG GACGCCACGGCCCCGAAGCCGCGAGTGACCGCGGCTCCGATCCCCCGGCGGGAGGCCTGCCCGAG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:70822008..70822121 26863196 MeRIP-seq:(Medium) rs1319427694 Functional Loss SNV dbSNP153 33..33 33 - - - 72106 RMVar_ID_72106 Human_SNP_ID_559882101 m1A Human chr14 - 70907523 70907523 70907523 CGCGGCCCGGCCCCCGCCACCCGCGGCCCGCCAGCGCCCCCACTGCCGCCGCCGCGACCCCCGCC CGCGGCCCGGCCCCCGCCACCCGCGGCCCGCCGGCGCCCCCACTGCCGCCGCCGCGACCCCCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70907483..70907900 26863196 MeRIP-seq:(Medium) rs1392967605 Functional Loss SNV dbSNP153 33..33 33 - - - 72107 RMVar_ID_72107 Human_SNP_ID_559882106 m1A Human chr14 - 70907537 70907537 70907537 CTAACACCCGGAGCCGCGGCCCGGCCCCCGCCACCCGCGGCCCGCCAGCGCCCCCACTGCCGCCG CTAACACCCGGAGCCGCGGCCCGGCCCCCGCCGCCCGCGGCCCGCCAGCGCCCCCACTGCCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:70907492..70907894 26863196 MeRIP-seq:(Medium) rs1013083933 Functional Loss SNV dbSNP153 33..33 33 - - - 72108 RMVar_ID_72108 Human_SNP_ID_559882107 m1A Human chr14 - 70907537 70907537 70907537 CTAACACCCGGAGCCGCGGCCCGGCCCCCGCCACCCGCGGCCCGCCAGCGCCCCCACTGCCGCCG CTAACACCCGGAGCCGCGGCCCGGCCCCCGCCCCCCGCGGCCCGCCAGCGCCCCCACTGCCGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:70907492..70907894 26863196 MeRIP-seq:(Medium) rs1013083933 Functional Loss SNV dbSNP153 33..33 33 - - - 72109 RMVar_ID_72109 Human_SNP_ID_559882135 m1A Human chr14 - 70907613 70907613 70907613 GAGGCGGCGAGCGGCGGGGCGGAGGACGGCGGAGAGGAGGAGACCGGCCTTCTGAGAGCCGCCGC GAGGCGGCGAGCGGCGGGGCGGAGGACGGCGGGGAGGAGGAGACCGGCCTTCTGAGAGCCGCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:70907515..70907651 26863410 MeRIP-seq:(Medium) rs148523058 Functional Loss SNV dbSNP153 33..33 33 - - - 72110 RMVar_ID_72110 Human_SNP_ID_559900000 m1A Human chr14 + 70972227 70972227 70972227 AGGGAGGATGGGGGCCCGCCAACTGAAAGGGGAAAGACTGAGGAGGAGCAGATTCAGGGTGGGGA AGGGAGGATGGGGGCCCGCCAACTGAAAGGGGCAAGACTGAGGAGGAGCAGATTCAGGGTGGGGA A C PCNX1 Ensembl:ENSG00000100731 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:70972079..70972373 26863196 MeRIP-seq:(Medium) rs1432525683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69303,RMVar_hsa_circ_85442,RMVar_hsa_circ_274798,RMVar_hsa_circ_312286,RMVar_hsa_circ_356179,RMVar_hsa_circ_167585,RMVar_hsa_circ_376214,RMVar_hsa_circ_120823,RMVar_hsa_circ_99201,RMVar_hsa_circ_127516,RMVar_hsa_circ_167587,RMVar_hsa_circ_167589,RMVar_hsa_circ_167588,RMVar_hsa_circ_167586,RMVar_hsa_circ_320723,RMVar_hsa_circ_369729,RMVar_hsa_circ_311868,RMVar_hsa_circ_294876,RMVar_hsa_circ_69410,RMVar_hsa_circ_105320,RMVar_hsa_circ_101126,RMVar_hsa_circ_167595,RMVar_hsa_circ_167597,RMVar_hsa_circ_167598,RMVar_hsa_circ_167599,RMVar_hsa_circ_167596,RMVar_hsa_circ_267774,RMVar_hsa_circ_345618,RMVar_hsa_circ_167594,RMVar_hsa_circ_301099,RMVar_hsa_circ_167600,RMVar_hsa_circ_167601 72111 RMVar_ID_72111 Human_SNP_ID_559984632 m1A Human chr14 + 71320500 71320499 71320501 GCGAGTTCAGTGCGTGCGTGAGCGAGTGAGCGAAAAGTCAGTGCAGCGCCGAGTCCCCGGCTGGA GCGAGTTCAGTGCGTGCGTGAGCGAGTGAGCG__AAGTCAGTGCAGCGCCGAGTCCCCGGCTGGA GAA G SIPA1L1 Ensembl:ENSG00000197555 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:71320451..71321300 26863196 MeRIP-seq:(Medium) rs1566878608 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18418002,Human_RBP_ID_23634610,Human_RBP_ID_24367897 Human_Splice_Rec_1531231,Human_Splice_Rec_1531241,Human_Splice_Rec_1531253,Human_Splice_Rec_1531269,Human_Splice_Rec_1531285,Human_Splice_Rec_1531299,Human_Splice_Rec_1531311 72112 RMVar_ID_72112 Human_SNP_ID_559984632 m1A Human chr14 + 71320501 71320499 71320501 CGAGTTCAGTGCGTGCGTGAGCGAGTGAGCGAAAAGTCAGTGCAGCGCCGAGTCCCCGGCTGGAG CGAGTTCAGTGCGTGCGTGAGCGAGTGAGCG__AAGTCAGTGCAGCGCCGAGTCCCCGGCTGGAG GAA G SIPA1L1 Ensembl:ENSG00000197555 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:71320497..71320627 26863196 MeRIP-seq:(Medium) rs1566878608 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18418002,Human_RBP_ID_24367897 Human_Splice_Rec_1531231,Human_Splice_Rec_1531241,Human_Splice_Rec_1531253,Human_Splice_Rec_1531269,Human_Splice_Rec_1531285,Human_Splice_Rec_1531299,Human_Splice_Rec_1531311 72113 RMVar_ID_72113 Human_SNP_ID_559984633 m1A Human chr14 + 71320500 71320500 71320500 GCGAGTTCAGTGCGTGCGTGAGCGAGTGAGCGAAAAGTCAGTGCAGCGCCGAGTCCCCGGCTGGA GCGAGTTCAGTGCGTGCGTGAGCGAGTGAGCGGAAAGTCAGTGCAGCGCCGAGTCCCCGGCTGGA A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:71320451..71321300 26863196 MeRIP-seq:(Medium) rs905430228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418002,Human_RBP_ID_23634610,Human_RBP_ID_24367897 Human_Splice_Rec_1531231,Human_Splice_Rec_1531241,Human_Splice_Rec_1531253,Human_Splice_Rec_1531269,Human_Splice_Rec_1531285,Human_Splice_Rec_1531299,Human_Splice_Rec_1531311 72114 RMVar_ID_72114 Human_SNP_ID_559984843 m1A Human chr14 + 71320938 71320938 71320938 TCCGGGAGCTCGGCCCCCGCCGGCCCCCCGCCAGCCTGTATTCCGGGTCCCCCTCGGAGCCAGCC TCCGGGAGCTCGGCCCCCGCCGGCCCCCCGCCGGCCTGTATTCCGGGTCCCCCTCGGAGCCAGCC A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:71320888..71321178 26863196 MeRIP-seq:(Medium) rs1320734757 Functional Loss SNV dbSNP153 33..33 33 - - - 72115 RMVar_ID_72115 Human_SNP_ID_559984943 m1A Human chr14 + 71321178 71321152 71321178 GGGACGCGCGGCGGCACCGGGAGGCCGGGCCGAGCGGTAAGTGGTCCCCGCGCCCGGGTCCTGGG GGGACGC__________________________GCGGTAAGTGGTCCCCGCGCCCGGGTCCTGGG CGCGGCGGCACCGGGAGGCCGGGCCGA C SIPA1L1 Ensembl:ENSG00000197555 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:71320917..71321200;chr14:71321077..71321200 26863196 MeRIP-seq:(Medium) rs1289348790 Functional Loss DEL dbSNP153 8..33 33 - - - Human_RBP_ID_22926487 Human_Splice_Rec_1531232,Human_Splice_Rec_1531233,Human_Splice_Rec_1531242,Human_Splice_Rec_1531243,Human_Splice_Rec_1531254,Human_Splice_Rec_1531255,Human_Splice_Rec_1531270,Human_Splice_Rec_1531271,Human_Splice_Rec_1531286,Human_Splice_Rec_1531287,Human_Splice_Rec_1531300,Human_Splice_Rec_1531301,Human_Splice_Rec_1531312,Human_Splice_Rec_1531313 72116 RMVar_ID_72116 Human_SNP_ID_559988819 m1A Human chr14 + 71337431 71337429 71337431 TAATTTATAAAGGAAAGAGGCTTAATGGACTCACAGTTCCACATGGCTGGGGAAGCCTCACAATC TAATTTATAAAGGAAAGAGGCTTAATGGACT__CAGTTCCACATGGCTGGGGAAGCCTCACAATC TCA T SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:71337430..71337513 26863196 MeRIP-seq:(Medium) rs1327187287 Functional Loss DEL dbSNP153 32..33 33 - - - 72117 RMVar_ID_72117 Human_SNP_ID_559992630 m1A Human chr14 - 71353640 71353640 71353640 AGGTCTAGTCACCATAATCACTCCCTCAGACCACCCCCACTGCCTCTTAACTGGCTCCCTACTTC AGGTCTAGTCACCATAATCACTCCCTCAGACCTCCCCCACTGCCTCTTAACTGGCTCCCTACTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:71353636..71353729 26863196 MeRIP-seq:(Medium) rs1473378854 Functional Loss SNV dbSNP153 33..33 33 - - - 72118 RMVar_ID_72118 Human_SNP_ID_559998322 m1A Human chr14 + 71377115 71377115 71377115 GGCTCCTCACTTTCCAGATGTGGCGGCCGGGCAGAGGGGCCCCCCCACCCCCCAGATGGGGCGGC GGCTCCTCACTTTCCAGATGTGGCGGCCGGGCGGAGGGGCCCCCCCACCCCCCAGATGGGGCGGC A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:71377105..71377418 26863196 MeRIP-seq:(Medium) rs1175089108 Functional Loss SNV dbSNP153 33..33 33 - - - 72119 RMVar_ID_72119 Human_SNP_ID_560026207 m1A Human chr14 + 71492131 71492120 71492132 TTTGGCTGTGTTGGGAAATATTGGCTACTACCAGGGCTGAGTGCAAAGAGGGTGGTATAGTAACT TTTGGCTGTGTTGGGAAATATT____________GGCTGAGTGCAAAGAGGGTGGTATAGTAACT TGGCTACTACCAG T SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:71492129..71492213 26863196 MeRIP-seq:(Medium) rs951660084 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_6380906 RMVar_hsa_circ_326686,RMVar_hsa_circ_303569,RMVar_hsa_circ_336115,RMVar_hsa_circ_342753,RMVar_hsa_circ_304615,RMVar_hsa_circ_282950,RMVar_hsa_circ_271774,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837,RMVar_hsa_circ_167693 72120 RMVar_ID_72120 Human_SNP_ID_560031249 m1A Human chr14 - 71512679 71512679 71512679 TCTTTATAGATGCACATTCCCACCCCCCTCCCAACCCCCCCAACCCCGGCTTCCCCCCACACACA TCTTTATAGATGCACATTCCCACCCCCCTCCCCACCCCCCCAACCCCGGCTTCCCCCCACACACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:71512677..71512772 26863196 MeRIP-seq:(Medium) rs997123771 Functional Loss SNV dbSNP153 33..33 33 - - - 72121 RMVar_ID_72121 Human_SNP_ID_560056837 m1A Human chr14 - 71616101 71616101 71616101 ATCTGAATAATCCACCTGCTTTCAGAACTTCAACTGCCACCTCAATGTTGACGACTCTCAGAGGT ATCTGAATAATCCACCTGCTTTCAGAACTTCAGCTGCCACCTCAATGTTGACGACTCTCAGAGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:71616095..71616189 26863196 MeRIP-seq:(Medium) rs761285705 Functional Loss SNV dbSNP153 33..33 33 - - - 72122 RMVar_ID_72122 Human_SNP_ID_560056948 m1A Human chr14 + 71616606 71616606 71616606 TGGGCAAATGGGTGGGGGTGGGGCTTTGGATCATACAGAAAAAGAAGCTAGAGTGTGGATGCTGG TGGGCAAATGGGTGGGGGTGGGGCTTTGGATCGTACAGAAAAAGAAGCTAGAGTGTGGATGCTGG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:71616567..71616673 26863196 MeRIP-seq:(Medium) rs994004663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34761,RMVar_hsa_circ_336115,RMVar_hsa_circ_342753,RMVar_hsa_circ_335518,RMVar_hsa_circ_167697,RMVar_hsa_circ_370002,RMVar_hsa_circ_360066,RMVar_hsa_circ_273909,RMVar_hsa_circ_167698,RMVar_hsa_circ_27310,RMVar_hsa_circ_167699 72123 RMVar_ID_72123 Human_SNP_ID_560056949 m1A Human chr14 + 71616606 71616606 71616606 TGGGCAAATGGGTGGGGGTGGGGCTTTGGATCATACAGAAAAAGAAGCTAGAGTGTGGATGCTGG TGGGCAAATGGGTGGGGGTGGGGCTTTGGATCTTACAGAAAAAGAAGCTAGAGTGTGGATGCTGG A T SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:71616567..71616673 26863196 MeRIP-seq:(Medium) rs994004663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34761,RMVar_hsa_circ_336115,RMVar_hsa_circ_342753,RMVar_hsa_circ_335518,RMVar_hsa_circ_167697,RMVar_hsa_circ_370002,RMVar_hsa_circ_360066,RMVar_hsa_circ_273909,RMVar_hsa_circ_167698,RMVar_hsa_circ_27310,RMVar_hsa_circ_167699 72124 RMVar_ID_72124 Human_SNP_ID_560321827 m1A Human chr14 - 72662275 72662275 72662275 TTAACTCTAAAGAAAAATGCCCCACATTTTAAATAAGAAAATAAAGATCAACTCTGCTCTCTCAG TTAACTCTAAAGAAAAATGCCCCACATTTTAAGTAAGAAAATAAAGATCAACTCTGCTCTCTCAG T C DPF3 Ensembl:ENSG00000205683 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3460433 GWAS_ID_8777,GWAS_ID_8778,GWAS_ID_8779 72125 RMVar_ID_72125 Human_SNP_ID_560321924 m1A Human chr14 + 72662722 72662722 72662722 AAACACACGCACAGGAGGGGGCTGGGCAAGGGAAGAGGAAGAAGAGGAGGAGGAGGAGGAGGTGC AAACACACGCACAGGAGGGGGCTGGGCAAGGGGAGAGGAAGAAGAGGAGGAGGAGGAGGAGGTGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:72662672..72662822 32194978 MeRIP-seq:(Medium) rs983725627 Functional Loss SNV dbSNP153 33..33 33 - - - 72126 RMVar_ID_72126 Human_SNP_ID_560388954 m1A Human chr14 - 72937994 72937994 72937994 GCTTCTTCTCCCATGTCGTCTTCTACTCTGCCAGCGACTTTTATTCATTTCTGTTCCTAAAAGAG GCTTCTTCTCCCATGTCGTCTTCTACTCTGCCGGCGACTTTTATTCATTTCTGTTCCTAAAAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:72937986..72938092 26863196 MeRIP-seq:(Medium) rs751470383 Functional Loss SNV dbSNP153 33..33 33 - - - 72127 RMVar_ID_72127 Human_SNP_ID_560395856 m1A Human chr14 + 72963098 72963098 72963098 AGTAAATACTGTCAGCCACAGCGTCACCAGAAAAGATAGAGGGATTTTCAGCTTGCTCTTGTGCT AGTAAATACTGTCAGCCACAGCGTCACCAGAATAGATAGAGGGATTTTCAGCTTGCTCTTGTGCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:72963048..72963225 26863196 MeRIP-seq:(Medium) rs1178384868 Functional Loss SNV dbSNP153 33..33 33 - - - 72128 RMVar_ID_72128 Human_SNP_ID_560409790 m1A Human chr14 + 73017651 73017651 73017651 AGTTCTCCTACTCCCTCACTCCTCCATCCAACATATCAGCACTCCTACTTTACCTACAAACTTTG AGTTCTCCTACTCCCTCACTCCTCCATCCAACGTATCAGCACTCCTACTTTACCTACAAACTTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73017638..73017742 26863196 MeRIP-seq:(Medium) rs528901956 Functional Loss SNV dbSNP153 33..33 33 - - - 72129 RMVar_ID_72129 Human_SNP_ID_560412650 m1A Human chr14 - 73027014 73027014 73027014 GAGGAGGGTGGCGGAGATGGAGATGAGGATGGATCTGCCGGTGTCCTGAGGAATAGCCTCTGCCC GAGGAGGGTGGCGGAGATGGAGATGAGGATGGCTCTGCCGGTGTCCTGAGGAATAGCCTCTGCCC T G ZFYVE1 Ensembl:ENSG00000165861 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73026932..73027047 26863196 MeRIP-seq:(Medium) rs1413839533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6381459 Human_Splice_Rec_1532417,Human_Splice_Rec_1532441,Human_Splice_Rec_1532463 72130 RMVar_ID_72130 Human_SNP_ID_560412652 m1A Human chr14 + 73027023 73027023 73027023 CTATTCCTCAGGACACCGGCAGATCCATCCTCATCTCCATCTCCGCCACCCTCCTCCTTCGTTGC CTATTCCTCAGGACACCGGCAGATCCATCCTCCTCTCCATCTCCGCCACCCTCCTCCTTCGTTGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73026954..73027090 26863196 MeRIP-seq:(Medium) rs941333795 Functional Loss SNV dbSNP153 33..33 33 - - - 72131 RMVar_ID_72131 Human_SNP_ID_560421371 m1A Human chr14 - 73058707 73058707 73058707 CGGTTTCCACACGCGTTCAGAGACACAAACTCACCCGCCGCTGAGGAAACGGTACTGCCTTCGCG CGGTTTCCACACGCGTTCAGAGACACAAACTCCCCCGCCGCTGAGGAAACGGTACTGCCTTCGCG T G AL442663.3 Ensembl:ENSG00000258813 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr14:73058676..73058725;chr14:73058523..73058774 32194978 MeRIP-seq:(Medium) rs976310711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1532536 Human_miRNA_ID_3208886 72132 RMVar_ID_72132 Human_SNP_ID_560426379 m1A Human chr14 - 73076335 73076335 73076335 GTTGGAGCAGGAGCCATAATGCTCATTGGTACAGGAATCATTGGGGTCCCTAAGAAAAGAAAAAC GTTGGAGCAGGAGCCATAATGCTCATTGGTACGGGAATCATTGGGGTCCCTAAGAAAAGAAAAAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73076326..73076375 32194978 MeRIP-seq:(Medium) rs1406558522 Functional Loss SNV dbSNP153 33..33 33 - - - 72133 RMVar_ID_72133 Human_SNP_ID_560433722 m1A Human chr14 + 73103331 73103331 73103331 GGAACGAGAAAGGGAAAGAGAACGTGAACGAGAAAAGGAGAAAGAACGGGAGCGGGAACGAGAAC GGAACGAGAAAGGGAAAGAGAACGTGAACGAGCAAAGGAGAAAGAACGGGAGCGGGAACGAGAAC A C RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:73103282..73103450 26863196 MeRIP-seq:(Medium) rs1228520965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4458,Human_RBP_ID_197250,Human_RBP_ID_231153,Human_RBP_ID_813043,Human_RBP_ID_9369167,Human_RBP_ID_12412202,Human_RBP_ID_17067520,Human_RBP_ID_18411097,Human_RBP_ID_22926360,Human_RBP_ID_23118239,Human_RBP_ID_23272482,Human_RBP_ID_23635261,Human_RBP_ID_24543698,Human_RBP_ID_25127688,Human_RBP_ID_26325207,Human_RBP_ID_27808404 RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_365770 72134 RMVar_ID_72134 Human_SNP_ID_560434729 m1A Human chr14 + 73105911 73105911 73105911 AAAGGGAACGAGAGCGGGAAAGAGAGAGAGAGAGAGAACGAGAGCGAGAACGAGAACGGGAGCGA AAAGGGAACGAGAGCGGGAAAGAGAGAGAGAGCGAGAACGAGAGCGAGAACGAGAACGGGAGCGA A C RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73105825..73106109 26863196 MeRIP-seq:(Medium) rs1015796307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39586,Human_RBP_ID_197095,Human_RBP_ID_231154,Human_RBP_ID_813044,Human_RBP_ID_1502466,Human_RBP_ID_5563459,Human_RBP_ID_9345016,Human_RBP_ID_17067522,Human_RBP_ID_22926492,Human_RBP_ID_23272483,Human_RBP_ID_23635269,Human_RBP_ID_24543700,Human_RBP_ID_25112662,Human_RBP_ID_26325210,Human_RBP_ID_27808405 Human_Splice_Rec_1532558,Human_Splice_Rec_1532608,Human_Splice_Rec_1532642,Human_Splice_Rec_1532718 RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_55992,RMVar_hsa_circ_365770 72135 RMVar_ID_72135 Human_SNP_ID_560434740 m1A Human chr14 + 73105927 73105922 73105928 GGAAAGAGAGAGAGAGAGAGAACGAGAGCGAGAACGAGAACGGGAGCGAGAGAGAGAGCGAGAGA GGAAAGAGAGAGAGAGAGAGAACGAGAG______CGAGAACGGGAGCGAGAGAGAGAGCGAGAGA GCGAGAA G RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:73105816..73106103;chr14:73103146..73107338 26863196 MeRIP-seq:(Medium) rs569416992 Functional Loss DEL dbSNP153,HGVD 29..34 33 - - - Human_RBP_ID_39586,Human_RBP_ID_197095,Human_RBP_ID_231154,Human_RBP_ID_813044,Human_RBP_ID_1502466,Human_RBP_ID_5563459,Human_RBP_ID_9345016,Human_RBP_ID_17067523,Human_RBP_ID_22926492,Human_RBP_ID_23272483,Human_RBP_ID_24543700,Human_RBP_ID_26325210,Human_RBP_ID_27808405 Human_Splice_Rec_1532558,Human_Splice_Rec_1532608,Human_Splice_Rec_1532642,Human_Splice_Rec_1532718 RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_55992,RMVar_hsa_circ_365770 72136 RMVar_ID_72136 Human_SNP_ID_560435654 m1A Human chr14 + 73109393 73109393 73109393 AGGTTGCGTGATAGAGAAAAGGAAATGGAAGCAGATGAACGAGATAGGAAGAGAGAGAAGGAGGA AGGTTGCGTGATAGAGAAAAGGAAATGGAAGCGGATGAACGAGATAGGAAGAGAGAGAAGGAGGA A G RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73109283..73111000 26863196 MeRIP-seq:(Medium) rs951037741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1502470,Human_RBP_ID_1823970,Human_RBP_ID_3944999,Human_RBP_ID_4300873,Human_RBP_ID_5563463,Human_RBP_ID_6381830,Human_RBP_ID_8250283,Human_RBP_ID_8409671,Human_RBP_ID_9369171,Human_RBP_ID_12412377,Human_RBP_ID_18980790,Human_RBP_ID_21969545,Human_RBP_ID_22927259,Human_RBP_ID_23635277,Human_RBP_ID_24543708,Human_RBP_ID_26325215,Human_RBP_ID_27808406 Human_Splice_Rec_1532564,Human_Splice_Rec_1532565,Human_Splice_Rec_1532614,Human_Splice_Rec_1532615,Human_Splice_Rec_1532648,Human_Splice_Rec_1532649,Human_Splice_Rec_1532724,Human_Splice_Rec_1532725,Human_Splice_Rec_1532744,Human_Splice_Rec_1532745,Human_Splice_Rec_1532756,Human_Splice_Rec_1532757,Human_Splice_Rec_1532765 Human_miRNA_ID_541713 RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_59694,RMVar_hsa_circ_44717,RMVar_hsa_circ_66288,RMVar_hsa_circ_55992,RMVar_hsa_circ_365770,RMVar_hsa_circ_60078,RMVar_hsa_circ_97514,RMVar_hsa_circ_167755 72137 RMVar_ID_72137 Human_SNP_ID_560436101 m1A Human chr14 + 73110881 73110881 73110881 AGGCGCAGGCAGCCACAAATAAAGCAAGAGCCAGAATCAGAAGAGGAGGAAGAAGAAAAGCAAGA AGGCGCAGGCAGCCACAAATAAAGCAAGAGCCCGAATCAGAAGAGGAGGAAGAAGAAAAGCAAGA A C RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:73110788..73110975 26863196 MeRIP-seq:(Medium) rs138412278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197098,Human_RBP_ID_882015,Human_RBP_ID_2425985,Human_RBP_ID_3945000,Human_RBP_ID_5522806,Human_RBP_ID_5563465,Human_RBP_ID_8230630,Human_RBP_ID_9369172,Human_RBP_ID_18980792,Human_RBP_ID_22045296,Human_RBP_ID_22926227,Human_RBP_ID_23644052,Human_RBP_ID_24543711,Human_RBP_ID_26324713,Human_RBP_ID_27808408 Human_Splice_Rec_1532566,Human_Splice_Rec_1532616,Human_Splice_Rec_1532650,Human_Splice_Rec_1532726,Human_Splice_Rec_1532746,Human_Splice_Rec_1532758,Human_Splice_Rec_1532766 RMVar_hsa_circ_68396,RMVar_hsa_circ_59694,RMVar_hsa_circ_44717,RMVar_hsa_circ_66288,RMVar_hsa_circ_55992,RMVar_hsa_circ_365770,RMVar_hsa_circ_343046 72138 RMVar_ID_72138 Human_SNP_ID_560442935 m1A Human chr14 - 73136527 73136527 73136527 CCGCCGCGGCTCGTAGCTCAGGTTCCTTCCAGACCAGCCGCTGTTTTGTTTCCGATGTGAAACCG CCGCCGCGGCTCGTAGCTCAGGTTCCTTCCAGCCCAGCCGCTGTTTTGTTTCCGATGTGAAACCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73136476..73136954 26863196 MeRIP-seq:(Medium) rs201430897 Functional Loss SNV dbSNP153 33..33 33 - - - 72139 RMVar_ID_72139 Human_SNP_ID_560442950 m1A Human chr14 + 73136561 73136561 73136561 TGGAAGGAACCTGAGCTACGAGCCGCGGCGGCAGCGGGGCGGCGGGGAAGCGTATGTGCGTGATG TGGAAGGAACCTGAGCTACGAGCCGCGGCGGCGGCGGGGCGGCGGGGAAGCGTATGTGCGTGATG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr14:73136451..73136696;chr14:73136484..73136637;chr14:73136451..73136738 26863196,26863410,26863196 MeRIP-seq:(Medium) rs200698508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813024,Human_RBP_ID_4308404,Human_RBP_ID_8230533,Human_RBP_ID_9323809,Human_RBP_ID_9417797,Human_RBP_ID_18418004,Human_RBP_ID_26325935 Human_Splice_Rec_1532775,Human_Splice_Rec_1532783,Human_Splice_Rec_1532789,Human_Splice_Rec_1532795,Human_Splice_Rec_1532801,Human_Splice_Rec_1532809,Human_Splice_Rec_1532815,Human_Splice_Rec_1532823,Human_Splice_Rec_1532831,Human_Splice_Rec_1532853,Human_Splice_Rec_1532861,Human_Splice_Rec_1532869,Human_Splice_Rec_1532879,Human_Splice_Rec_1532887,Human_Splice_Rec_1532909,Human_Splice_Rec_1532919 72140 RMVar_ID_72140 Human_SNP_ID_560443007 m1A Human chr14 - 73136764 73136764 73136764 CTCTCTCCACCCGGCCGCGCCCGAAGCCCGAGAAACGGGCCGCCCCTCCTGGTTTCCCACACGGG CTCTCTCCACCCGGCCGCGCCCGAAGCCCGAGCAACGGGCCGCCCCTCCTGGTTTCCCACACGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:73136756..73136928 26863196 MeRIP-seq:(Medium) rs958019425 Functional Loss SNV dbSNP153 33..33 33 - - - 72141 RMVar_ID_72141 Human_SNP_ID_560445911 m1A Human chr14 + 73147842 73147842 73147842 CTGCAAGTGACAACAGCCTTTGCGGTCCTTAGACAGCTTGGCCTGGAGGAGAACACATGAAAGAA CTGCAAGTGACAACAGCCTTTGCGGTCCTTAGGCAGCTTGGCCTGGAGGAGAACACATGAAAGAA A G PSEN1 Ensembl:ENSG00000080815 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73147739..73147875 26863196 MeRIP-seq:(Medium) rs200583938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882018,Human_RBP_ID_1824025,Human_RBP_ID_4308902,Human_RBP_ID_12413232,Human_RBP_ID_18656050 Human_Splice_Rec_1532768,Human_Splice_Rec_1532769,Human_Splice_Rec_1532778,Human_Splice_Rec_1532779,Human_Splice_Rec_1532784,Human_Splice_Rec_1532785,Human_Splice_Rec_1532790,Human_Splice_Rec_1532791,Human_Splice_Rec_1532796,Human_Splice_Rec_1532797,Human_Splice_Rec_1532802,Human_Splice_Rec_1532803,Human_Splice_Rec_1532810,Human_Splice_Rec_1532811,Human_Splice_Rec_1532818,Human_Splice_Rec_1532819,Human_Splice_Rec_1532824,Human_Splice_Rec_1532825,Human_Splice_Rec_1532832,Human_Splice_Rec_1532833,Human_Splice_Rec_1532856,Human_Splice_Rec_1532857,Human_Splice_Rec_1532862,Human_Splice_Rec_1532863,Human_Splice_Rec_1532872,Human_Splice_Rec_1532873,Human_Splice_Rec_1532882,Human_Splice_Rec_1532883,Human_Splice_Rec_1532888,Human_Splice_Rec_1532889,Human_Splice_Rec_1532910,Human_Splice_Rec_1532911,Human_Splice_Rec_1532926,Human_Splice_Rec_1532927,Human_Splice_Rec_1532932,Human_Splice_Rec_1532933,Human_Splice_Rec_1532953 RMVar_hsa_circ_167762,RMVar_hsa_circ_272739,RMVar_hsa_circ_281918,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_285631,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_126482,RMVar_hsa_circ_271393,RMVar_hsa_circ_96822,RMVar_hsa_circ_167764,RMVar_hsa_circ_167766,RMVar_hsa_circ_167768,RMVar_hsa_circ_60156,RMVar_hsa_circ_167767,RMVar_hsa_circ_167765,RMVar_hsa_circ_167763,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757 72142 RMVar_ID_72142 Human_SNP_ID_560462183 m1A Human chr14 + 73211942 73211942 73211942 GCAGTATCCTCGCTGGTGAAGACCCAGAGGAAAGTATGTGCATTTCTCTATGTTGCAAAGTCATG GCAGTATCCTCGCTGGTGAAGACCCAGAGGAATGTATGTGCATTTCTCTATGTTGCAAAGTCATG A T PSEN1 Ensembl:ENSG00000080815 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73211901..73219143 32194978 MeRIP-seq:(Medium) rs1555357544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9370272 Human_Splice_Rec_1532849,Human_Splice_Rec_1532905,Human_Splice_Rec_1532949,Human_Splice_Rec_1532973,Human_Splice_Rec_1532991,Human_Splice_Rec_1533025,Human_Splice_Rec_1533035 RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882,RMVar_hsa_circ_323779,RMVar_hsa_circ_167772,RMVar_hsa_circ_269707 72143 RMVar_ID_72143 Human_SNP_ID_560472917 m1A Human chr14 + 73251820 73251820 73251820 TGAGCGACTCCATGCCCGGGGCCCCACCTCGGAGCCCCTGGTCATCGAGGTAAATGGGGGTGTGG TGAGCGACTCCATGCCCGGGGCCCCACCTCGGCGCCCCTGGTCATCGAGGTAAATGGGGGTGTGG A C PAPLN Ensembl:ENSG00000100767 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73251676..73252765 32194978 MeRIP-seq:(Medium) rs758739222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1533053,Human_Splice_Rec_1533105,Human_Splice_Rec_1533155,Human_Splice_Rec_1533203,Human_Splice_Rec_1533253,Human_Splice_Rec_1533303 RMVar_hsa_circ_61023,RMVar_hsa_circ_167775,RMVar_hsa_circ_310202 72144 RMVar_ID_72144 Human_SNP_ID_560475916 m1A Human chr14 + 73260806 73260806 73260806 CGTATGGTGGTGACAGCACCGGGGGCATGCCCAGGTCAAGGGCAGTGGCTTCTACAGTAAGTGTC CGTATGGTGGTGACAGCACCGGGGGCATGCCCGGGTCAAGGGCAGTGGCTTCTACAGTAAGTGTC A G PAPLN Ensembl:ENSG00000100767 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73259492..73260806 32194978 MeRIP-seq:(Medium) rs1354375885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944576 Human_Splice_Rec_1533068,Human_Splice_Rec_1533069,Human_Splice_Rec_1533120,Human_Splice_Rec_1533121,Human_Splice_Rec_1533170,Human_Splice_Rec_1533171,Human_Splice_Rec_1533218,Human_Splice_Rec_1533219,Human_Splice_Rec_1533268,Human_Splice_Rec_1533269,Human_Splice_Rec_1533318,Human_Splice_Rec_1533319 RMVar_hsa_circ_61023 72145 RMVar_ID_72145 Human_SNP_ID_560525601 m1A Human chr14 - 73457466 73457466 73457466 GAGAGAGTAATGGTTTCGTGGAACTGGCTAGGACAGTAGATATATGAGAAATTAACAGTGGAGCC GAGAGAGTAATGGTTTCGTGGAACTGGCTAGGGCAGTAGATATATGAGAAATTAACAGTGGAGCC T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73457464..73457687 26863196 MeRIP-seq:(Medium) rs910912811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5565131,Human_RBP_ID_12415100 72146 RMVar_ID_72146 Human_SNP_ID_560525824 m1A Human chr14 - 73458156 73458156 73458156 CCGGCGGCCACTGTGTGAGGAGTAGGTATCTGAGGAAACGGAAGCGGCCAGGGTCCCAGAGAGGG CCGGCGGCCACTGTGTGAGGAGTAGGTATCTGTGGAAACGGAAGCGGCCAGGGTCCCAGAGAGGG T A NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73458154..73458258 26863196 MeRIP-seq:(Medium) rs1415079028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3468017,Human_RBP_ID_5565235,Human_RBP_ID_12415104 72147 RMVar_ID_72147 Human_SNP_ID_560534192 m1A Human chr14 - 73491023 73491023 73491023 CGCCTCAACGGCCCTGCACTGGCCTGGAGCCCATCCATGGCCAGACCACACCAGTCTTCCCCGCC CGCCTCAACGGCCCTGCACTGGCCTGGAGCCCTTCCATGGCCAGACCACACCAGTCTTCCCCGCC T A HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:73490981..73491087;chr14:73490976..73491318 26863196 MeRIP-seq:(Medium) rs747930339 Functional Loss SNV dbSNP153 33..33 33 - - - 72148 RMVar_ID_72148 Human_SNP_ID_560534193 m1A Human chr14 - 73491023 73491023 73491023 CGCCTCAACGGCCCTGCACTGGCCTGGAGCCCATCCATGGCCAGACCACACCAGTCTTCCCCGCC CGCCTCAACGGCCCTGCACTGGCCTGGAGCCCGTCCATGGCCAGACCACACCAGTCTTCCCCGCC T C HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:73490981..73491087;chr14:73490976..73491318 26863196 MeRIP-seq:(Medium) rs747930339 Functional Loss SNV dbSNP153 33..33 33 - - - 72149 RMVar_ID_72149 Human_SNP_ID_560534214 m1A Human chr14 - 73491048 73491048 73491048 CTTGCGCCGGCGCTTCGGCCGCCCGCGCCTCAACGGCCCTGCACTGGCCTGGAGCCCATCCATGG CTTGCGCCGGCGCTTCGGCCGCCCGCGCCTCAGCGGCCCTGCACTGGCCTGGAGCCCATCCATGG T C HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73490997..73491310 26863196 MeRIP-seq:(Medium) rs763287247 Functional Loss SNV dbSNP153 33..33 33 - - - 72150 RMVar_ID_72150 Human_SNP_ID_560534216 m1A Human chr14 + 73491051 73491051 73491051 TGGATGGGCTCCAGGCCAGTGCAGGGCCGTTGAGGCGCGGGCGGCCGAAGCGCCGGCGCAAGCCC TGGATGGGCTCCAGGCCAGTGCAGGGCCGTTGGGGCGCGGGCGGCCGAAGCGCCGGCGCAAGCCC A G RIOX1 Ensembl:ENSG00000170468 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73491007..73491330 26863196 MeRIP-seq:(Medium) rs1300284297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301104,Human_RBP_ID_5141150 72151 RMVar_ID_72151 Human_SNP_ID_560534424 m1A Human chr14 + 73491448 73491448 73491448 GGAGGTGCCCGCCGCGCCGGTCCGGGTGGTGGAGACCTCGGCCCTGCTGTGCACCGCGCAACACT GGAGGTGCCCGCCGCGCCGGTCCGGGTGGTGGTGACCTCGGCCCTGCTGTGCACCGCGCAACACT A T RIOX1 Ensembl:ENSG00000170468 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73491399..73491675 26863196 MeRIP-seq:(Medium) rs925000101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17853099 72152 RMVar_ID_72152 Human_SNP_ID_560534468 m1A Human chr14 + 73491529 73491529 73491529 GTCCGGGGCCCCTGCGACGGCGTCGGGGCCGCAGGTGGATAACACGGGTGGGGAGCCGGCCTGGG GTCCGGGGCCCCTGCGACGGCGTCGGGGCCGCTGGTGGATAACACGGGTGGGGAGCCGGCCTGGG A T RIOX1 Ensembl:ENSG00000170468 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:73491478..73491607 26863196 MeRIP-seq:(Medium) rs1486628693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8796103 72153 RMVar_ID_72153 Human_SNP_ID_560534622 m1A Human chr14 - 73491841 73491841 73491841 CGGCGGCGGGCAGCGCGCGGCCGGGTGGGTTCAGGGTCTCGCGTCGTCCGTTGATGTAGCGAGCG CGGCGGCGGGCAGCGCGCGGCCGGGTGGGTTCTGGGTCTCGCGTCGTCCGTTGATGTAGCGAGCG T A HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73491791..73491862 26863196 MeRIP-seq:(Medium) rs765306782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1533793 72154 RMVar_ID_72154 Human_SNP_ID_560534623 m1A Human chr14 - 73491841 73491841 73491841 CGGCGGCGGGCAGCGCGCGGCCGGGTGGGTTCAGGGTCTCGCGTCGTCCGTTGATGTAGCGAGCG CGGCGGCGGGCAGCGCGCGGCCGGGTGGGTTCCGGGTCTCGCGTCGTCCGTTGATGTAGCGAGCG T G HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73491791..73491862 26863196 MeRIP-seq:(Medium) rs765306782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1533793 72155 RMVar_ID_72155 Human_SNP_ID_560535120 m1A Human chr14 + 73493167 73493167 73493167 AAGGAAAAGGAGAAGTTGGAGGTGGAAAAAAAACCCTTGATCCGTGATCATTTCAGAGCACCAAC AAGGAAAAGGAGAAGTTGGAGGTGGAAAAAAACCCCTTGATCCGTGATCATTTCAGAGCACCAAC A C RIOX1 Ensembl:ENSG00000170468 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:73493076..73495279 26863196 MeRIP-seq:(Medium) rs756570824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17853106 Human_miRNA_ID_726385 72156 RMVar_ID_72156 Human_SNP_ID_560546236 m1A Human chr14 - 73537458 73537455 73537458 CACGGCGATTCGCACCGGTTCGTCCCAGCAGCAGCGGCCCGCGGGCTCCAGGATCAGCGTCGCCG CACGGCGATTCGCACCGGTTCGTCCCAGCAGC___GGCCCGCGGGCTCCAGGATCAGCGTCGCCG CGCT C HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73537418..73537490 26863196 MeRIP-seq:(Medium) rs1383391754 Functional Loss DEL dbSNP153 33..35 33 - - - 72157 RMVar_ID_72157 Human_SNP_ID_560546237 m1A Human chr14 - 73537458 73537458 73537458 CACGGCGATTCGCACCGGTTCGTCCCAGCAGCAGCGGCCCGCGGGCTCCAGGATCAGCGTCGCCG CACGGCGATTCGCACCGGTTCGTCCCAGCAGCCGCGGCCCGCGGGCTCCAGGATCAGCGTCGCCG T G HEATR4 Ensembl:ENSG00000187105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73537418..73537490 26863196 MeRIP-seq:(Medium) rs1384428765 Functional Loss SNV dbSNP153 33..33 33 - - - 72158 RMVar_ID_72158 Human_SNP_ID_560553004 m1A Human chr14 + 73569395 73569395 73569395 GGCGCAGTTCCTGGGGTCTCCACAGCTGAGGCAGGTTGGTCAGATCATTAGGGTTCCTGCTCGGA GGCGCAGTTCCTGGGGTCTCCACAGCTGAGGCCGGTTGGTCAGATCATTAGGGTTCCTGCTCGGA A C ACOT2 Ensembl:ENSG00000119673 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73569345..73569546 32194978 MeRIP-seq:(Medium) rs572796695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451389,Human_RBP_ID_884016,Human_RBP_ID_4308905 Human_Splice_Rec_1533893 RMVar_hsa_circ_167793,RMVar_hsa_circ_107415 72159 RMVar_ID_72159 Human_SNP_ID_560553070 m1A Human chr14 - 73569503 73569503 73569503 ACGCGCGCAGCGTGACCGGCTGCTCCGGGGCTAGGCCGCGCACGGCGATTCGCACCGGTTCGTCC ACGCGCGCAGCGTGACCGGCTGCTCCGGGGCTGGGCCGCGCACGGCGATTCGCACCGGTTCGTCC T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:73569345..73569745 26863410 MeRIP-seq:(Medium) rs774249499 Functional Loss SNV dbSNP153 33..33 33 - - - 72160 RMVar_ID_72160 Human_SNP_ID_560553263 m1A Human chr14 + 73569793 73569793 73569793 ACGACCCCGACCCCGGGCGGCTGCTGTGCCAGACGCGGCACGAGCGCTACTTCCTCCCGCCCGGG ACGACCCCGACCCCGGGCGGCTGCTGTGCCAGGCGCGGCACGAGCGCTACTTCCTCCCGCCCGGG A G ACOT2 Ensembl:ENSG00000119673 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73569685..73569845 26863196 MeRIP-seq:(Medium) rs1231350535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22439282 Human_Splice_Rec_1533897,Human_Splice_Rec_1533901,Human_Splice_Rec_1533905 RMVar_hsa_circ_167793,RMVar_hsa_circ_107415 72161 RMVar_ID_72161 Human_SNP_ID_560553275 m1A Human chr14 - 73569808 73569806 73569809 CGGCTCGCGCCGCACCCCGGGCGGGAGGAAGTAGCGCTCGTGCCGCGTCTGGCACAGCAGCCGCC CGGCTCGCGCCGCACCCCGGGCGGGAGGAAG___CGCTCGTGCCGCGTCTGGCACAGCAGCCGCC GCTA G AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73569758..73569920 26863196 MeRIP-seq:(Medium) rs779701848 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4301202 72162 RMVar_ID_72162 Human_SNP_ID_560553310 m1A Human chr14 - 73569848 73569848 73569848 GCGGCAGGAAGAGCGTGCCTCGCACCCGGCCCACGCGCACCGGCTCGCGCCGCACCCCGGGCGGG GCGGCAGGAAGAGCGTGCCTCGCACCCGGCCCGCGCGCACCGGCTCGCGCCGCACCCCGGGCGGG T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:73569644..73573398 26863196 MeRIP-seq:(Medium) rs200192188 Functional Loss SNV dbSNP153 33..33 33 - - - 72163 RMVar_ID_72163 Human_SNP_ID_560554592 m1A Human chr14 - 73573409 73573409 73573409 GCAGGCCACCTCCAGTTCCGAACATGTCCACAATCCCAGGAAAGGGCCCAGGTTCTTGGGAAGAA GCAGGCCACCTCCAGTTCCGAACATGTCCACAGTCCCAGGAAAGGGCCCAGGTTCTTGGGAAGAA T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr14:73569844..73574311;chr14:73569644..73573498 32194978 MeRIP-seq:(Medium) rs1301411147 Functional Loss SNV dbSNP153 33..33 33 - - - 72164 RMVar_ID_72164 Human_SNP_ID_560560707 m1A Human chr14 + 73592297 73592297 73592297 TGTCGTGGAGTTGGAGGTGCTGGACGGCCACGACCCCGAGCCTGGACGGCTGCTGTGCCAGGCGC TGTCGTGGAGTTGGAGGTGCTGGACGGCCACGCCCCCGAGCCTGGACGGCTGCTGTGCCAGGCGC A C ACOT4 Ensembl:ENSG00000177465 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73592193..73592339 26863196 MeRIP-seq:(Medium) rs768965606 Functional Loss SNV dbSNP153 33..33 33 - - - 72165 RMVar_ID_72165 Human_SNP_ID_560573903 m1A Human chr14 - 73645074 73645074 73645074 CAGTCACCCTTTTCCACTCCCAATCTTCTCTCAGCTTTGGCTACGCGGCCCGAAAGGTACTCACC CAGTCACCCTTTTCCACTCCCAATCTTCTCTCGGCTTTGGCTACGCGGCCCGAAAGGTACTCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73645069..73645319 26863196 MeRIP-seq:(Medium) rs745929634 Functional Loss SNV dbSNP153 33..33 33 - - - 72166 RMVar_ID_72166 Human_SNP_ID_560573904 m1A Human chr14 - 73645074 73645074 73645074 CAGTCACCCTTTTCCACTCCCAATCTTCTCTCAGCTTTGGCTACGCGGCCCGAAAGGTACTCACC CAGTCACCCTTTTCCACTCCCAATCTTCTCTCCGCTTTGGCTACGCGGCCCGAAAGGTACTCACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73645069..73645319 26863196 MeRIP-seq:(Medium) rs745929634 Functional Loss SNV dbSNP153 33..33 33 - - - 72167 RMVar_ID_72167 Human_SNP_ID_560586930 m1A Human chr14 + 73698015 73698015 73698015 CAGTAGGCAAGCTTGAAGCCATGTTGATATGGATATGTTTTCTAAAAGTAACCCTGGAAGTGAAT CAGTAGGCAAGCTTGAAGCCATGTTGATATGGGTATGTTTTCTAAAAGTAACCCTGGAAGTGAAT A G DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17182488 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_304 GWAS_ID_8780,GWAS_ID_8781,GWAS_ID_8782 72168 RMVar_ID_72168 Human_SNP_ID_560590950 m1A Human chr14 - 73712624 73712624 73712624 CCGTGAGGAGGAAGCCAAGGAGGAGGAGGAGGAGGCTGAGGCCACCCTTCTGCAGTTAGGCCTGG CCGTGAGGAGGAAGCCAAGGAGGAGGAGGAGGCGGCTGAGGCCACCCTTCTGCAGTTAGGCCTGG T G PNMA1 Ensembl:ENSG00000176903 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73712601..73712625 32194978 MeRIP-seq:(Medium) rs1327194282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6382962 72169 RMVar_ID_72169 Human_SNP_ID_560591120 m1A Human chr14 - 73713052 73713052 73713052 GAGGTCCTAGAGGAGTGGCAGGTGTCCGATGTAGAAAAGAGGCGGCGGTTGATGGAGAGTCTTAG GAGGTCCTAGAGGAGTGGCAGGTGTCCGATGTTGAAAAGAGGCGGCGGTTGATGGAGAGTCTTAG T A PNMA1 Ensembl:ENSG00000176903 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73713001..73713175 32194978 MeRIP-seq:(Medium) rs750338011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301266,Human_RBP_ID_23635727 72170 RMVar_ID_72170 Human_SNP_ID_560591350 m1A Human chr14 + 73713591 73713591 73713591 TGGGATGCCCCAGACTAACAGAGCTCTCTGGGAGTTCACATCCATCCCCCGGCACCAGTCTTCCA TGGGATGCCCCAGACTAACAGAGCTCTCTGGGCGTTCACATCCATCCCCCGGCACCAGTCTTCCA A C NONHSAG015431.2 RNACentral:URS00009BAFD6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:73713541..73713669;chr14:73713540..73713697 26863196 MeRIP-seq:(Medium) rs370288059 Functional Loss SNV dbSNP153 33..33 33 - - - 72171 RMVar_ID_72171 Human_SNP_ID_560591351 m1A Human chr14 + 73713591 73713591 73713591 TGGGATGCCCCAGACTAACAGAGCTCTCTGGGAGTTCACATCCATCCCCCGGCACCAGTCTTCCA TGGGATGCCCCAGACTAACAGAGCTCTCTGGGGGTTCACATCCATCCCCCGGCACCAGTCTTCCA A G NONHSAG015431.2 RNACentral:URS00009BAFD6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:73713541..73713669;chr14:73713540..73713697 26863196 MeRIP-seq:(Medium) rs370288059 Functional Loss SNV dbSNP153 33..33 33 - - - 72172 RMVar_ID_72172 Human_SNP_ID_560591586 m1A Human chr14 + 73714278 73714278 73714278 AGGAAAGTCGGAGAAGCGAGGCTGGAGACAGCAGAGGCGAGGGTGGGAAGGGGCGGCCGCGGCGG AGGAAAGTCGGAGAAGCGAGGCTGGAGACAGCGGAGGCGAGGGTGGGAAGGGGCGGCCGCGGCGG A G NONHSAG015431.2 RNACentral:URS00009BAFD6 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:73713674..73714400 26863410 MeRIP-seq:(Medium) rs1473910232 Functional Loss SNV dbSNP153 33..33 33 - - - 72173 RMVar_ID_72173 Human_SNP_ID_560592875 m1A Human chr14 - 73718549 73718549 73718549 CGGTCCCCTCGGGAGGGACTCCACCGCCTCTCACACTCCGATTTCTGCTGCTCTGCTGCCCCGCA CGGTCCCCTCGGGAGGGACTCCACCGCCTCTCTCACTCCGATTTCTGCTGCTCTGCTGCCCCGCA T A MIDEAS Ensembl:ENSG00000156030 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr14:73718501..73718550;chr14:73718498..73718582 26863196 MeRIP-seq:(Medium) rs974465016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23208568,Human_RBP_ID_27432749 Human_miRNA_ID_94985,Human_miRNA_ID_1770438 72174 RMVar_ID_72174 Human_SNP_ID_560593030 m1A Human chr14 - 73718947 73718944 73718947 CGCATATGAAGAGCCACGCAGAGCAGGAGAAGAAGGCTGCAGCGCTGAGGCTGAAGGAGAAAGAG CGCATATGAAGAGCCACGCAGAGCAGGAGAAG___GCTGCAGCGCTGAGGCTGAAGGAGAAAGAG CCTT C MIDEAS Ensembl:ENSG00000156030 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73718896..73719009 26863196 MeRIP-seq:(Medium) rs944178418 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_451456,Human_RBP_ID_881020,Human_RBP_ID_4301363,Human_RBP_ID_26325937 Human_Splice_Rec_1534102 72175 RMVar_ID_72175 Human_SNP_ID_560593231 m1A Human chr14 - 73719400 73719400 73719400 GAGAAGCCAAGGGAAGGGACAGGGAAGTCACGAAGGGCACTACCTTTTTCAGAGAAGAAGAAAAA GAGAAGCCAAGGGAAGGGACAGGGAAGTCACGTAGGGCACTACCTTTTTCAGAGAAGAAGAAAAA T A MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73719298..73719425 26863196 MeRIP-seq:(Medium) rs148823944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40889,Human_RBP_ID_6383050,Human_RBP_ID_17853180 Human_Splice_Rec_1534101 Human_miRNA_ID_490945,Human_miRNA_ID_494202 RMVar_hsa_circ_545 72176 RMVar_ID_72176 Human_SNP_ID_560593747 m1A Human chr14 - 73721367 73721367 73721367 GGTGCCAGAGATCCAAGAGAAGGAGGAGCAGGAAGAGGGGCGAGAGCGCAGCAGGCGGGCAGCGG GGTGCCAGAGATCCAAGAGAAGGAGGAGCAGGGAGAGGGGCGAGAGCGCAGCAGGCGGGCAGCGG T C MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:73721316..73721457;chr14:73721274..73721525 26863196 MeRIP-seq:(Medium) rs745418178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40890,Human_RBP_ID_3944580,Human_RBP_ID_5140887,Human_RBP_ID_5522808,Human_RBP_ID_18189488,Human_RBP_ID_24367127,Human_RBP_ID_26325229,Human_RBP_ID_26431693 Human_Splice_Rec_1534045,Human_Splice_Rec_1534057,Human_Splice_Rec_1534079,Human_Splice_Rec_1534099,Human_Splice_Rec_1534103,Human_Splice_Rec_1534125,Human_Splice_Rec_1534147 RMVar_hsa_circ_545 72177 RMVar_ID_72177 Human_SNP_ID_560593748 m1A Human chr14 - 73721370 73721370 73721370 GGAGGTGCCAGAGATCCAAGAGAAGGAGGAGCAGGAAGAGGGGCGAGAGCGCAGCAGGCGGGCAG GGAGGTGCCAGAGATCCAAGAGAAGGAGGAGCTGGAAGAGGGGCGAGAGCGCAGCAGGCGGGCAG T A MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73721259..73721500 26863196 MeRIP-seq:(Medium) rs139139732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40890,Human_RBP_ID_3944580,Human_RBP_ID_4301367,Human_RBP_ID_5140887,Human_RBP_ID_5522808,Human_RBP_ID_18189488,Human_RBP_ID_24367127,Human_RBP_ID_26325229,Human_RBP_ID_26431693 Human_Splice_Rec_1534045,Human_Splice_Rec_1534057,Human_Splice_Rec_1534079,Human_Splice_Rec_1534099,Human_Splice_Rec_1534103,Human_Splice_Rec_1534125,Human_Splice_Rec_1534147 RMVar_hsa_circ_545 72178 RMVar_ID_72178 Human_SNP_ID_560593749 m1A Human chr14 - 73721370 73721370 73721370 GGAGGTGCCAGAGATCCAAGAGAAGGAGGAGCAGGAAGAGGGGCGAGAGCGCAGCAGGCGGGCAG GGAGGTGCCAGAGATCCAAGAGAAGGAGGAGCGGGAAGAGGGGCGAGAGCGCAGCAGGCGGGCAG T C MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73721259..73721500 26863196 MeRIP-seq:(Medium) rs139139732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40890,Human_RBP_ID_3944580,Human_RBP_ID_4301367,Human_RBP_ID_5140887,Human_RBP_ID_5522808,Human_RBP_ID_18189488,Human_RBP_ID_24367127,Human_RBP_ID_26325229,Human_RBP_ID_26431693 Human_Splice_Rec_1534045,Human_Splice_Rec_1534057,Human_Splice_Rec_1534079,Human_Splice_Rec_1534099,Human_Splice_Rec_1534103,Human_Splice_Rec_1534125,Human_Splice_Rec_1534147 RMVar_hsa_circ_545 72179 RMVar_ID_72179 Human_SNP_ID_560598197 m1A Human chr14 + 73738675 73738675 73738675 GTCGCGTGCTCTGGATCACTCCGCCCCGTAGCACCTGCCCACAGTCCCCTGTGCTCACTGCCCTC GTCGCGTGCTCTGGATCACTCCGCCCCGTAGCTCCTGCCCACAGTCCCCTGTGCTCACTGCCCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73738626..73738729 26863196 MeRIP-seq:(Medium) rs1289781112 Functional Loss SNV dbSNP153 33..33 33 - - - 72180 RMVar_ID_72180 Human_SNP_ID_560598468 m1A Human chr14 - 73739274 73739274 73739274 CCGCCCCCAAACCCGGTGGCTGCCTTCCCTCCACAGAAGCAGCAGCAGCAGCAGCAACCACAGCA CCGCCCCCAAACCCGGTGGCTGCCTTCCCTCCGCAGAAGCAGCAGCAGCAGCAGCAACCACAGCA T C MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73739223..73739324 32194978 MeRIP-seq:(Medium) rs916002989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301391 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 72181 RMVar_ID_72181 Human_SNP_ID_560598530 m1A Human chr14 + 73739409 73739409 73739409 GACTGGTTTGGGGGTTTCTTGGCTGCGTGGAAAGAATTCAGGGGTGCCTGGGGCCGCCCTACCTC GACTGGTTTGGGGGTTTCTTGGCTGCGTGGAAGGAATTCAGGGGTGCCTGGGGCCGCCCTACCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:73739220..73739468 26863196 MeRIP-seq:(Medium) rs756882365 Functional Loss SNV dbSNP153 33..33 33 - - - 72182 RMVar_ID_72182 Human_SNP_ID_560598532 m1A Human chr14 - 73739413 73739413 73739413 GCTGGAGGTAGGGCGGCCCCAGGCACCCCTGAATTCTTTCCACGCAGCCAAGAAACCCCCAAACC GCTGGAGGTAGGGCGGCCCCAGGCACCCCTGATTTCTTTCCACGCAGCCAAGAAACCCCCAAACC T A MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73739288..73739508 26863196 MeRIP-seq:(Medium) rs371001327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2140261,Human_miRNA_ID_2765767 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 72183 RMVar_ID_72183 Human_SNP_ID_560598631 m1A Human chr14 - 73739683 73739683 73739683 CAACTCTGTGATGGCTCCAGGGCGGGGCCCGGAGCGTGGAGGAGGTGGGGGTGTCAGTGACAGCA CAACTCTGTGATGGCTCCAGGGCGGGGCCCGGCGCGTGGAGGAGGTGGGGGTGTCAGTGACAGCA T G MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73739422..73739773 32194978 MeRIP-seq:(Medium) rs1410047802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880590 Human_miRNA_ID_208053,Human_miRNA_ID_2016438 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 72184 RMVar_ID_72184 Human_SNP_ID_560598771 m1A Human chr14 + 73740048 73740048 73740048 CCAACTGAGCCCTGGCGGTGAGATCCCCTTCAACAGTCGCCCATCCCCTGGGGAAACGTCCTGCT CCAACTGAGCCCTGGCGGTGAGATCCCCTTCAGCAGTCGCCCATCCCCTGGGGAAACGTCCTGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73739872..73760015 32194978 MeRIP-seq:(Medium) rs772057230 Functional Loss SNV dbSNP153 33..33 33 - - - 72185 RMVar_ID_72185 Human_SNP_ID_560598814 m1A Human chr14 - 73740250 73740250 73740250 ACACTGTCACTGCTCTTCCCTCTGCAGGTGCCAGAACCCTGTGGAGCATCATGAACTGGGAAGAG ACACTGTCACTGCTCTTCCCTCTGCAGGTGCCGGAACCCTGTGGAGCATCATGAACTGGGAAGAG T C MIDEAS Ensembl:ENSG00000156030 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:73739924..73740274;chr14:73740052..73740294;chr14:73739945..73740275 26863196 MeRIP-seq:(Medium) rs1169610966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22648494,Human_RBP_ID_22737624 Human_Splice_Rec_1534026,Human_Splice_Rec_1534060,Human_Splice_Rec_1534128,Human_Splice_Rec_1534158,Human_Splice_Rec_1534162 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 72186 RMVar_ID_72186 Human_SNP_ID_560599879 m1A Human chr14 - 73745140 73745140 73745140 CCAGCATCTTGAGGAGCTCTCATGTGCACCAGAGAGCCCAGAAGTCAGGAGCAGGCAGGAGCCCA CCAGCATCTTGAGGAGCTCTCATGTGCACCAGCGAGCCCAGAAGTCAGGAGCAGGCAGGAGCCCA T G MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73745138..73745368 26863196 MeRIP-seq:(Medium) rs1383070928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167804,RMVar_hsa_circ_107985 72187 RMVar_ID_72187 Human_SNP_ID_560607626 m1A Human chr14 - 73777382 73777382 73777382 AACTGTAGCTAAATTGAGGAGAAAAGAAATGTATTGGAAGGCTATCTGGTGGCTCACTGAATGTC AACTGTAGCTAAATTGAGGAGAAAAGAAATGTGTTGGAAGGCTATCTGGTGGCTCACTGAATGTC T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:73777361..73777566;chr14:73777370..73777480 26863196 MeRIP-seq:(Medium) rs1331200392 Functional Loss SNV dbSNP153 33..33 33 - - - 72188 RMVar_ID_72188 Human_SNP_ID_560620922 m1A Human chr14 - 73829975 73829975 73829975 GTAAATGGGAGAGAAGAGGAAAAGAAGGAAAGAAATGAGAGCCACATATCTACTGGCAAAAGGAA GTAAATGGGAGAGAAGAGGAAAAGAAGGAAAGCAATGAGAGCCACATATCTACTGGCAAAAGGAA T G LINC02274 Ensembl:ENSG00000258586 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73829941..73830023 26863196 MeRIP-seq:(Medium) rs1210268271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1534171 72189 RMVar_ID_72189 Human_SNP_ID_560627130 m1A Human chr14 + 73852696 73852696 73852696 TAAAGTGGTTGGTAGGAGGAGCCACAGGGCTCAGGGAGGTCACTGAGAAAGGGAAGAGCAAGATA TAAAGTGGTTGGTAGGAGGAGCCACAGGGCTCTGGGAGGTCACTGAGAAAGGGAAGAGCAAGATA A T PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73852690..73852822 26863196 MeRIP-seq:(Medium) rs554167802 Functional Loss SNV dbSNP153 33..33 33 - - - 72190 RMVar_ID_72190 Human_SNP_ID_560632184 m1A Human chr14 + 73874094 73874094 73874094 ACACCTTGGCAGCTATCTCAAGTCGTTGATGGAGGAGGTATTGGAATTATAGAAGAAAGCAAACA ACACCTTGGCAGCTATCTCAAGTCGTTGATGGGGGAGGTATTGGAATTATAGAAGAAAGCAAACA A G PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11159042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3945015,Human_RBP_ID_23635788,Human_RBP_ID_26325232 Human_Splice_Rec_1534178,Human_Splice_Rec_1534196,Human_Splice_Rec_1534214,Human_Splice_Rec_1534228,Human_Splice_Rec_1534244,Human_Splice_Rec_1534254,Human_Splice_Rec_1534268 Human_miRNA_ID_2418543,Human_miRNA_ID_3092017 GWAS_ID_8783,GWAS_ID_8784,GWAS_ID_8785,GWAS_ID_8786,GWAS_ID_8787,GWAS_ID_8788,GWAS_ID_8789,GWAS_ID_8790,GWAS_ID_8791,GWAS_ID_8792,GWAS_ID_8793,GWAS_ID_8794,GWAS_ID_8795,GWAS_ID_8796,GWAS_ID_8797,GWAS_ID_8798,GWAS_ID_8799,GWAS_ID_8800,GWAS_ID_8801,GWAS_ID_8802,GWAS_ID_8803,GWAS_ID_8804,GWAS_ID_8805,GWAS_ID_8806,GWAS_ID_8807,GWAS_ID_8808,GWAS_ID_8809,GWAS_ID_8810,GWAS_ID_8811,GWAS_ID_8812,GWAS_ID_8813,GWAS_ID_8814,GWAS_ID_8815,GWAS_ID_8816,GWAS_ID_8817,GWAS_ID_8818,GWAS_ID_8819,GWAS_ID_8820,GWAS_ID_8821,GWAS_ID_8822,GWAS_ID_8823,GWAS_ID_8824,GWAS_ID_8825,GWAS_ID_8826,GWAS_ID_8827,GWAS_ID_8828,GWAS_ID_8829,GWAS_ID_8830,GWAS_ID_8831,GWAS_ID_8832,GWAS_ID_8833,GWAS_ID_8834,GWAS_ID_8835 RMVar_hsa_circ_40215,RMVar_hsa_circ_305319,RMVar_hsa_circ_349232,RMVar_hsa_circ_355280,RMVar_hsa_circ_67974,RMVar_hsa_circ_65339,RMVar_hsa_circ_82128,RMVar_hsa_circ_101082,RMVar_hsa_circ_167807,RMVar_hsa_circ_167808,RMVar_hsa_circ_167806,RMVar_hsa_circ_359577,RMVar_hsa_circ_84235,RMVar_hsa_circ_57260,RMVar_hsa_circ_167811,RMVar_hsa_circ_61290,RMVar_hsa_circ_167812,RMVar_hsa_circ_353654,RMVar_hsa_circ_167810,RMVar_hsa_circ_365109,RMVar_hsa_circ_350552 72191 RMVar_ID_72191 Human_SNP_ID_560632185 m1A Human chr14 + 73874094 73874094 73874094 ACACCTTGGCAGCTATCTCAAGTCGTTGATGGAGGAGGTATTGGAATTATAGAAGAAAGCAAACA ACACCTTGGCAGCTATCTCAAGTCGTTGATGGTGGAGGTATTGGAATTATAGAAGAAAGCAAACA A T PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11159042 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3945015,Human_RBP_ID_23635788,Human_RBP_ID_26325232 Human_Splice_Rec_1534178,Human_Splice_Rec_1534196,Human_Splice_Rec_1534214,Human_Splice_Rec_1534228,Human_Splice_Rec_1534244,Human_Splice_Rec_1534254,Human_Splice_Rec_1534268 Human_miRNA_ID_2418543,Human_miRNA_ID_3092017 GWAS_ID_8783,GWAS_ID_8784,GWAS_ID_8785,GWAS_ID_8786,GWAS_ID_8787,GWAS_ID_8788,GWAS_ID_8789,GWAS_ID_8790,GWAS_ID_8791,GWAS_ID_8792,GWAS_ID_8793,GWAS_ID_8794,GWAS_ID_8795,GWAS_ID_8796,GWAS_ID_8797,GWAS_ID_8798,GWAS_ID_8799,GWAS_ID_8800,GWAS_ID_8801,GWAS_ID_8802,GWAS_ID_8803,GWAS_ID_8804,GWAS_ID_8805,GWAS_ID_8806,GWAS_ID_8807,GWAS_ID_8808,GWAS_ID_8809,GWAS_ID_8810,GWAS_ID_8811,GWAS_ID_8812,GWAS_ID_8813,GWAS_ID_8814,GWAS_ID_8815,GWAS_ID_8816,GWAS_ID_8817,GWAS_ID_8818,GWAS_ID_8819,GWAS_ID_8820,GWAS_ID_8821,GWAS_ID_8822,GWAS_ID_8823,GWAS_ID_8824,GWAS_ID_8825,GWAS_ID_8826,GWAS_ID_8827,GWAS_ID_8828,GWAS_ID_8829,GWAS_ID_8830,GWAS_ID_8831,GWAS_ID_8832,GWAS_ID_8833,GWAS_ID_8834,GWAS_ID_8835 RMVar_hsa_circ_40215,RMVar_hsa_circ_305319,RMVar_hsa_circ_349232,RMVar_hsa_circ_355280,RMVar_hsa_circ_67974,RMVar_hsa_circ_65339,RMVar_hsa_circ_82128,RMVar_hsa_circ_101082,RMVar_hsa_circ_167807,RMVar_hsa_circ_167808,RMVar_hsa_circ_167806,RMVar_hsa_circ_359577,RMVar_hsa_circ_84235,RMVar_hsa_circ_57260,RMVar_hsa_circ_167811,RMVar_hsa_circ_61290,RMVar_hsa_circ_167812,RMVar_hsa_circ_353654,RMVar_hsa_circ_167810,RMVar_hsa_circ_365109,RMVar_hsa_circ_350552 72192 RMVar_ID_72192 Human_SNP_ID_560632981 m1A Human chr14 - 73877156 73877156 73877156 ATAATTCTCAGAAAGTTTACCTGCCCAGCCACAGATCCACAGGCACCTGCGGCCCCACTGACAAC ATAATTCTCAGAAAGTTTACCTGCCCAGCCACGGATCCACAGGCACCTGCGGCCCCACTGACAAC T C AC005520.7 Ensembl:ENSG00000273711 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73877105..73880092 32194978 MeRIP-seq:(Medium) rs1259503072 Functional Loss SNV dbSNP153 33..33 33 - - - 72193 RMVar_ID_72193 Human_SNP_ID_560636882 m1A Human chr14 - 73892029 73892029 73892029 GTAAGATGTTGTACTAGGTGGGTAATCAATGTAACCTAGAATAGGGGTAAAAAAGAGAGAGGGGG GTAAGATGTTGTACTAGGTGGGTAATCAATGTTACCTAGAATAGGGGTAAAAAAGAGAGAGGGGG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73892022..73893302 32194978 MeRIP-seq:(Medium) rs758651596 Functional Loss SNV dbSNP153 33..33 33 - - - 72194 RMVar_ID_72194 Human_SNP_ID_560645939 m1A Human chr14 - 73928253 73928253 73928253 GTCCTTCTGCCTGTTATATTCTTCCAACTCCTACTTCTCCATCAAGATGATGTCTATTCATCCCT GTCCTTCTGCCTGTTATATTCTTCCAACTCCTGCTTCTCCATCAAGATGATGTCTATTCATCCCT T C AC005480.1 Ensembl:ENSG00000258891 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73928216..73928360 26863196 MeRIP-seq:(Medium) rs1203606094 Functional Loss SNV dbSNP153 33..33 33 - - - 72195 RMVar_ID_72195 Human_SNP_ID_560650056 m1A Human chr14 - 73944606 73944606 73944606 GAAGAGGCCGAGTGCCACAGGCAGTTCCGGGCACAGCCTGTGCCTGCACATGTCTACCTGCCCCT GAAGAGGCCGAGTGCCACAGGCAGTTCCGGGCCCAGCCTGTGCCTGCACATGTCTACCTGCCCCT T G FAM161B Ensembl:ENSG00000156050 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73944556..73944805 32194978 MeRIP-seq:(Medium) rs751459531 Functional Loss SNV dbSNP153 33..33 33 - - - 72196 RMVar_ID_72196 Human_SNP_ID_560651479 m1A Human chr14 + 73950063 73950063 73950063 GCTGGACAGAGGCAGCAGCGACAGTGACAGCGATAGTGGCAGCAGCGGTGGCAGCGAGAGCTATG GCTGGACAGAGGCAGCAGCGACAGTGACAGCGGTAGTGGCAGCAGCGGTGGCAGCGAGAGCTATG A G COQ6 Ensembl:ENSG00000119723 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73949991..73950105 26863196 MeRIP-seq:(Medium) rs780415251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167830,RMVar_hsa_circ_100411 72197 RMVar_ID_72197 Human_SNP_ID_560651674 m1A Human chr14 - 73950346 73950344 73950346 GAGCTGCACGCACAGCCCCGCATCGGCTGACAAGCCGGGCCGCCATGGTGCAGACCTGCGCCGTC GAGCTGCACGCACAGCCCCGCATCGGCTGACA__CCGGGCCGCCATGGTGCAGACCTGCGCCGTC GCT G FAM161B Ensembl:ENSG00000156050 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:73950317..73950459 26863196 MeRIP-seq:(Medium) rs752687942 Functional Loss DEL dbSNP153 33..34 33 - - - 72198 RMVar_ID_72198 Human_SNP_ID_560651694 m1A Human chr14 - 73950367 73950367 73950367 ACACCAGCGGGCCGCTGTGGGGAGCTGCACGCACAGCCCCGCATCGGCTGACAAGCCGGGCCGCC ACACCAGCGGGCCGCTGTGGGGAGCTGCACGCGCAGCCCCGCATCGGCTGACAAGCCGGGCCGCC T C FAM161B Ensembl:ENSG00000156050 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:73950317..73950443 26863196 MeRIP-seq:(Medium) rs775635349 Functional Loss SNV dbSNP153 33..33 33 - - - 72199 RMVar_ID_72199 Human_SNP_ID_560651711 m1A Human chr14 - 73950402 73950402 73950402 GGTGTCTGTTGAGGCGCCGGACCACCTGCGCCAGGACACCAGCGGGCCGCTGTGGGGAGCTGCAC GGTGTCTGTTGAGGCGCCGGACCACCTGCGCCTGGACACCAGCGGGCCGCTGTGGGGAGCTGCAC T A FAM161B Ensembl:ENSG00000156050 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73950351..73950500 32194978 MeRIP-seq:(Medium) rs1367774676 Functional Loss SNV dbSNP153 33..33 33 - - - 72200 RMVar_ID_72200 Human_SNP_ID_560653294 m1A Human chr14 - 73955882 73955882 73955882 AACTGCTTAGTGAGAGCATGCATGATGACATCATTCTCCACGATATAGCCCATGTCATCTAAATT AACTGCTTAGTGAGAGCATGCATGATGACATCGTTCTCCACGATATAGCCCATGTCATCTAAATT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73955814..73955964 32194978 MeRIP-seq:(Medium) rs1306809044 Functional Loss SNV dbSNP153 33..33 33 - - - 72201 RMVar_ID_72201 Human_SNP_ID_560669838 m1A Human chr14 + 74018970 74018970 74018970 GGAGCGGCAGAAGCGGAGCGGGGGCGAGGGCAAGGTAGCCGCGGCCACGCTGGCTGCGGCATGGA GGAGCGGCAGAAGCGGAGCGGGGGCGAGGGCAGGGTAGCCGCGGCCACGCTGGCTGCGGCATGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:74018947..74019014 26863196 MeRIP-seq:(Medium) rs1254977313 Functional Loss SNV dbSNP153 33..33 33 - - - 72202 RMVar_ID_72202 Human_SNP_ID_560670063 m1A Human chr14 + 74019504 74019501 74019505 AGCCAAGATGCCGTCGAAGGGAAAGGACAAAAAGAAAGGCAAGAGCAAAGGCAAAGACACGAAGT AGCCAAGATGCCGTCGAAGGGAAAGGACAA____AAAGGCAAGAGCAAAGGCAAAGACACGAAGT AAAAG A BBOF1 Ensembl:ENSG00000119636 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74019402..74022933 26863196 MeRIP-seq:(Medium) rs777963786 Functional Loss DEL dbSNP153 31..34 33 - - - Human_Splice_Rec_1534961,Human_Splice_Rec_1534983,Human_Splice_Rec_1534993,Human_Splice_Rec_1535001 72203 RMVar_ID_72203 Human_SNP_ID_560670064 m1A Human chr14 + 74019504 74019504 74019504 AGCCAAGATGCCGTCGAAGGGAAAGGACAAAAAGAAAGGCAAGAGCAAAGGCAAAGACACGAAGT AGCCAAGATGCCGTCGAAGGGAAAGGACAAAACGAAAGGCAAGAGCAAAGGCAAAGACACGAAGT A C BBOF1 Ensembl:ENSG00000119636 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74019402..74022933 26863196 MeRIP-seq:(Medium) rs1349354109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1534961,Human_Splice_Rec_1534983,Human_Splice_Rec_1534993,Human_Splice_Rec_1535001 72204 RMVar_ID_72204 Human_SNP_ID_560672490 m1A Human chr14 + 74029118 74029118 74029118 ATATTGGTTTTAGTATTGTGTGAAACTAGTCTACTTAATAAAGGTAGACATAGAGCAGTTTCTTT ATATTGGTTTTAGTATTGTGTGAAACTAGTCTGCTTAATAAAGGTAGACATAGAGCAGTTTCTTT A G BBOF1 Ensembl:ENSG00000119636 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:74029116..74029302 26863196 MeRIP-seq:(Medium) rs1484264536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73664,RMVar_hsa_circ_310095,RMVar_hsa_circ_360696,RMVar_hsa_circ_337141,RMVar_hsa_circ_293401,RMVar_hsa_circ_167843,RMVar_hsa_circ_167844,RMVar_hsa_circ_167845 72205 RMVar_ID_72205 Human_SNP_ID_560685991 m1A Human chr14 - 74084383 74084383 74084383 GAGCTAGGGCGGCCGAGAGCCATGGCGGCGCTATTGGCGGCGGCGGCAGTGCGAGCCCGGATCCT GAGCTAGGGCGGCCGAGAGCCATGGCGGCGCTGTTGGCGGCGGCGGCAGTGCGAGCCCGGATCCT T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:74084307..74084413 26863196 MeRIP-seq:(Medium) rs754069309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301611 72206 RMVar_ID_72206 Human_SNP_ID_560696388 m1A Human chr14 - 74129131 74129127 74129131 TGTTTCCATTTCCTACCTTCCACTCATTCCTCACTCCATTTCAAACTGCCTCCACCATCCCACTA TGTTTCCATTTCCTACCTTCCACTCATTCCTC____CATTTCAAACTGCCTCCACCATCCCACTA GGAGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74129107..74129200 26863196 MeRIP-seq:(Medium) rs1417529484 Functional Loss DEL dbSNP153 33..36 33 - - - 72207 RMVar_ID_72207 Human_SNP_ID_560735308 m1A Human chr14 + 74286422 74286422 74286422 TCAGTCCTCCTGGTCTCTCCTGAGGGCCGCCGACCCGCCACAGTGTGGCTCTCCTTCCAAAAGCC TCAGTCCTCCTGGTCTCTCCTGAGGGCCGCCGCCCCGCCACAGTGTGGCTCTCCTTCCAAAAGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:74286375..74286562 26863196 MeRIP-seq:(Medium) rs975349818 Functional Loss SNV dbSNP153 33..33 33 - - - 72208 RMVar_ID_72208 Human_SNP_ID_560735329 m1A Human chr14 + 74286468 74286468 74286468 GGCTCTCCTTCCAAAAGCCAGAGCTTCATTCCACTTTGATTCTCATCAGCTCCCATCTTCCTCCT GGCTCTCCTTCCAAAAGCCAGAGCTTCATTCCGCTTTGATTCTCATCAGCTCCCATCTTCCTCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74286418..74286547 26863196 MeRIP-seq:(Medium) rs772523388 Functional Loss SNV dbSNP153 33..33 33 - - - 72209 RMVar_ID_72209 Human_SNP_ID_560735386 m1A Human chr14 - 74286605 74286600 74286606 GCCAGAGGCCCCTCAAAACGGGGAGTAGCAGTAGCAGAGAGAACCGAGTGGCCTCCTCTGCCAGC GCCAGAGGCCCCTCAAAACGGGGAGTAGCAG______AGAGAACCGAGTGGCCTCCTCTGCCAGC TCTGCTA T ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:74286602..74286698 26863196 MeRIP-seq:(Medium) rs1370368395 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_12418878 RMVar_hsa_circ_91051,RMVar_hsa_circ_167854 72210 RMVar_ID_72210 Human_SNP_ID_560785430 m1A Human chr14 + 74486403 74486403 74486403 TCAGCTGGCAGGGTTGGGTGGGGCATGGGCTCACATTCACTTCCTTTATAACTCCATCCACAGAA TCAGCTGGCAGGGTTGGGTGGGGCATGGGCTCGCATTCACTTCCTTTATAACTCCATCCACAGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74480720..74493348 32194978 MeRIP-seq:(Medium) rs1334912147 Functional Loss SNV dbSNP153 33..33 33 - - - 72211 RMVar_ID_72211 Human_SNP_ID_560786992 m1A Human chr14 + 74493273 74493273 74493273 CCAGGAGCAGGAATGTAGCTGCCAGGAAACGCATCGCGGATAACGAAGTTCCAAGCTCGGGAAAG CCAGGAGCAGGAATGTAGCTGCCAGGAAACGCGTCGCGGATAACGAAGTTCCAAGCTCGGGAAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74493226..74493300 26863196 MeRIP-seq:(Medium) rs1555346368 Functional Loss SNV dbSNP153 33..33 33 - - - 72212 RMVar_ID_72212 Human_SNP_ID_560787256 m1A Human chr14 + 74493844 74493844 74493844 CGCAGAGAGCGGTCACTCCCTGGCCGAGGGGCAGGTACCAAGACTAGAAAGGCACCTGGAAAGGG CGCAGAGAGCGGTCACTCCCTGGCCGAGGGGCTGGTACCAAGACTAGAAAGGCACCTGGAAAGGG A T ISCA2 Ensembl:ENSG00000165898 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:74493801..74493903 26863196 MeRIP-seq:(Medium) rs1207642936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308918 Human_Splice_Rec_1535615,Human_Splice_Rec_1535621,Human_Splice_Rec_1535625,Human_Splice_Rec_1535629 72213 RMVar_ID_72213 Human_SNP_ID_560787329 m1A Human chr14 - 74494099 74494099 74494099 GCGGATCTGCCCTTCGCCGGCCTCGGGGCTGGAGGACGACGCCTCCCGACGCGCCTGGGGTCCCA GCGGATCTGCCCTTCGCCGGCCTCGGGGCTGGGGGACGACGCCTCCCGACGCGCCTGGGGTCCCA T C NPC2 Ensembl:ENSG00000119655 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:74494031..74494098 26863196 MeRIP-seq:(Medium) rs1179386242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1535595 72214 RMVar_ID_72214 Human_SNP_ID_560789458 m1A Human chr14 + 74502762 74502762 74502762 GAGTGACCGGCTGTGTTGGGGAAGGCAGGCTCAGGGACGGTGTCCTCGGGGCCCAGGTAGTTGTA GAGTGACCGGCTGTGTTGGGGAAGGCAGGCTCGGGGACGGTGTCCTCGGGGCCCAGGTAGTTGTA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74502711..74503578 32194978 MeRIP-seq:(Medium) rs561011462 Functional Loss SNV dbSNP153 33..33 33 - - - 72215 RMVar_ID_72215 Human_SNP_ID_560814464 m1A Human chr14 - 74603704 74603704 74603704 TTGTGTTGACTCTGTTTTGGTGACCCCACAGGAGGAACGTCTGCGGGGGACAGTGCTGCCCAGGA TTGTGTTGACTCTGTTTTGGTGACCCCACAGGGGGAACGTCTGCGGGGGACAGTGCTGCCCAGGA T C LTBP2 Ensembl:ENSG00000119681 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74603683..74612382 32194978 MeRIP-seq:(Medium) rs1249566598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1535634,Human_Splice_Rec_1535635,Human_Splice_Rec_1535704,Human_Splice_Rec_1535705,Human_Splice_Rec_1535776,Human_Splice_Rec_1535777 RMVar_hsa_circ_99761,RMVar_hsa_circ_167915,RMVar_hsa_circ_124346,RMVar_hsa_circ_167916,RMVar_hsa_circ_342570 72216 RMVar_ID_72216 Human_SNP_ID_560828676 m1A Human chr14 - 74663532 74663532 74663532 GTCTTTACCTCACCTGCTCCCTGCCCATATCTACCACAGGCCACTTTGGCATGGTATGTAAGCTG GTCTTTACCTCACCTGCTCCCTGCCCATATCTCCCACAGGCCACTTTGGCATGGTATGTAAGCTG T G AREL1 Ensembl:ENSG00000119682 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1045430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19978857 Human_Splice_Rec_1535865 Human_miRNA_ID_1165884,Human_miRNA_ID_2846392,Human_miRNA_ID_2849413 GWAS_ID_8836,GWAS_ID_8837,GWAS_ID_8838,GWAS_ID_8839,GWAS_ID_8840,GWAS_ID_8841 RMVar_hsa_circ_75966,RMVar_hsa_circ_167926 72217 RMVar_ID_72217 Human_SNP_ID_560828714 m1A Human chr14 + 74663687 74663687 74663687 ATGTCTGTAACTTGCGCCCAGAAGCTCCAGAGAGCATGGGAGCCAACTGGATGACAGGAGAGTGG ATGTCTGTAACTTGCGCCCAGAAGCTCCAGAGGGCATGGGAGCCAACTGGATGACAGGAGAGTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74663597..74663846 32194978 MeRIP-seq:(Medium) rs746900273 Functional Loss SNV dbSNP153 33..33 33 - - - 72218 RMVar_ID_72218 Human_SNP_ID_560830589 m1A Human chr14 + 74670863 74670863 74670863 TAGCTCAAACCATTCCCGGCGAGGCCCTCCCCAGTCCAGAGCTGAAAAGCATAATGAAAATAAAA TAGCTCAAACCATTCCCGGCGAGGCCCTCCCCCGTCCAGAGCTGAAAAGCATAATGAAAATAAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74670776..74671463 32194978 MeRIP-seq:(Medium) rs771203415 Functional Loss SNV dbSNP153 33..33 33 - - - 72219 RMVar_ID_72219 Human_SNP_ID_560831849 m1A Human chr14 + 74675777 74675777 74675777 TCAGGGGTGTGGCACTCAGAGGGCGAGTCTTCATCTTCCTCGTCAACAGCAGTGGATGGCCGGCG TCAGGGGTGTGGCACTCAGAGGGCGAGTCTTCCTCTTCCTCGTCAACAGCAGTGGATGGCCGGCG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74675726..74675930 32194978 MeRIP-seq:(Medium) rs771440340 Functional Loss SNV dbSNP153 33..33 33 - - - 72220 RMVar_ID_72220 Human_SNP_ID_560831850 m1A Human chr14 + 74675777 74675777 74675777 TCAGGGGTGTGGCACTCAGAGGGCGAGTCTTCATCTTCCTCGTCAACAGCAGTGGATGGCCGGCG TCAGGGGTGTGGCACTCAGAGGGCGAGTCTTCGTCTTCCTCGTCAACAGCAGTGGATGGCCGGCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74675726..74675930 32194978 MeRIP-seq:(Medium) rs771440340 Functional Loss SNV dbSNP153 33..33 33 - - - 72221 RMVar_ID_72221 Human_SNP_ID_560833908 m1A Human chr14 + 74683445 74683445 74683445 TGGGCTCCTGAAGGACTTCCTGGGTCACTGGAATTTCCACTGCTAGCTCGACATGAGAGATGTGA TGGGCTCCTGAAGGACTTCCTGGGTCACTGGATTTTCCACTGCTAGCTCGACATGAGAGATGTGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74683394..74684513 32194978 MeRIP-seq:(Medium) rs1202136268 Functional Loss SNV dbSNP153 33..33 33 - - - 72222 RMVar_ID_72222 Human_SNP_ID_560841052 m1A Human chr14 + 74713041 74713041 74713041 GGGCTCCCCACTCTCCCACCAACAGACCCCAGAGTTGGTCTCCACCCGGCCTGGGAACCGGCTCG GGGCTCCCCACTCTCCCACCAACAGACCCCAGCGTTGGTCTCCACCCGGCCTGGGAACCGGCTCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:74712918..74713053;chr14:74712946..74713056;chr14:74712957..74713040 26863196 MeRIP-seq:(Medium) rs755695104 Functional Loss SNV dbSNP153 33..33 33 - - - 72223 RMVar_ID_72223 Human_SNP_ID_560841055 m1A Human chr14 - 74713043 74713043 74713043 CCCGAGCCGGTTCCCAGGCCGGGTGGAGACCAACTCTGGGGTCTGTTGGTGGGAGAGTGGGGAGC CCCGAGCCGGTTCCCAGGCCGGGTGGAGACCAGCTCTGGGGTCTGTTGGTGGGAGAGTGGGGAGC T C AREL1 Ensembl:ENSG00000119682 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:74712968..74713053 26863196 MeRIP-seq:(Medium) rs753842281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301851 72224 RMVar_ID_72224 Human_SNP_ID_560841056 m1A Human chr14 - 74713043 74713043 74713043 CCCGAGCCGGTTCCCAGGCCGGGTGGAGACCAACTCTGGGGTCTGTTGGTGGGAGAGTGGGGAGC CCCGAGCCGGTTCCCAGGCCGGGTGGAGACCACCTCTGGGGTCTGTTGGTGGGAGAGTGGGGAGC T G AREL1 Ensembl:ENSG00000119682 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:74712968..74713053 26863196 MeRIP-seq:(Medium) rs753842281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301851 72225 RMVar_ID_72225 Human_SNP_ID_560841060 m1A Human chr14 - 74713047 74713047 74713047 ATCCCCCGAGCCGGTTCCCAGGCCGGGTGGAGACCAACTCTGGGGTCTGTTGGTGGGAGAGTGGG ATCCCCCGAGCCGGTTCCCAGGCCGGGTGGAGGCCAACTCTGGGGTCTGTTGGTGGGAGAGTGGG T C AREL1 Ensembl:ENSG00000119682 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:74712915..74713063 26863196 MeRIP-seq:(Medium) rs778745727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451776,Human_RBP_ID_4301851 72226 RMVar_ID_72226 Human_SNP_ID_560841268 m1A Human chr14 + 74713499 74713499 74713499 TAAAATTTCTGTTTCAAGGGGAAGCAAAAGAAAACAAGGAAGTATGCGACCATGAAGCGAATGCT TAAAATTTCTGTTTCAAGGGGAAGCAAAAGAACACAAGGAAGTATGCGACCATGAAGCGAATGCT A C FCF1 Ensembl:ENSG00000119616 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:74713151..74714950 26863196 MeRIP-seq:(Medium) rs766772477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23636380 Human_Splice_Rec_1536120,Human_Splice_Rec_1536130,Human_Splice_Rec_1536131,Human_Splice_Rec_1536144,Human_Splice_Rec_1536145,Human_Splice_Rec_1536158,Human_Splice_Rec_1536159,Human_Splice_Rec_1536168,Human_Splice_Rec_1536169,Human_Splice_Rec_1536182,Human_Splice_Rec_1536183,Human_Splice_Rec_1536196,Human_Splice_Rec_1536197 72227 RMVar_ID_72227 Human_SNP_ID_560841803 m1A Human chr14 - 74715793 74715793 74715793 AAATCCTAAAAAGGAAGGCAAGGAAGAAAGTAATATCATTATCTTAATCTCAGCTCCCCTGGCAA AAATCCTAAAAAGGAAGGCAAGGAAGAAAGTAGTATCATTATCTTAATCTCAGCTCCCCTGGCAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:74715789..74715966 26863196 MeRIP-seq:(Medium) rs764439067 Functional Loss SNV dbSNP153 33..33 33 - - - 72228 RMVar_ID_72228 Human_SNP_ID_560846817 m1A Human chr14 + 74735841 74735841 74735841 AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCACTGTGCCTGGCCTGCTCAC AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTGCAGACATGAGCCACTGTGCCTGGCCTGCTCAC A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs907147969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301883,Human_RBP_ID_6384465,Human_RBP_ID_17562957,Human_RBP_ID_23161158,Human_RBP_ID_26430518 Human_miRNA_ID_1080194 72229 RMVar_ID_72229 Human_SNP_ID_560846818 m1A Human chr14 + 74735841 74735841 74735841 AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCACTGTGCCTGGCCTGCTCAC AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTTCAGACATGAGCCACTGTGCCTGGCCTGCTCAC A T FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs907147969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301883,Human_RBP_ID_6384465,Human_RBP_ID_17562957,Human_RBP_ID_23161158,Human_RBP_ID_26430518 Human_miRNA_ID_1080194 72230 RMVar_ID_72230 Human_SNP_ID_560846868 m1A Human chr14 + 74736031 74736031 74736031 TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTAGCTGGGACTATAGGTGCGTGCCACCACGTCCA TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTCGCTGGGACTATAGGTGCGTGCCACCACGTCCA A C FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs973688358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451794,Human_RBP_ID_4301884,Human_RBP_ID_26431709 72231 RMVar_ID_72231 Human_SNP_ID_560846869 m1A Human chr14 + 74736031 74736031 74736031 TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTAGCTGGGACTATAGGTGCGTGCCACCACGTCCA TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTGGCTGGGACTATAGGTGCGTGCCACCACGTCCA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs973688358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451794,Human_RBP_ID_4301884,Human_RBP_ID_26431709 72232 RMVar_ID_72232 Human_SNP_ID_560846932 m1A Human chr14 + 74736291 74736291 74736291 AAAATTAGCTGGGTATGGTGTCACGTGCCTGTAATCCCAGCCACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTATGGTGTCACGTGCCTGTGATCCCAGCCACTGGGGAGGCTGAGGCAGGAGA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1467519301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301893,Human_RBP_ID_26431713 72233 RMVar_ID_72233 Human_SNP_ID_560846936 m1A Human chr14 + 74736301 74736301 74736301 GGGTATGGTGTCACGTGCCTGTAATCCCAGCCACTGGGGAGGCTGAGGCAGGAGAACCTCTTGAA GGGTATGGTGTCACGTGCCTGTAATCCCAGCCGCTGGGGAGGCTGAGGCAGGAGAACCTCTTGAA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1370812834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431713 Human_miRNA_ID_504494,Human_miRNA_ID_511707 72234 RMVar_ID_72234 Human_SNP_ID_560846947 m1A Human chr14 + 74736362 74736362 74736362 TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCATTCCAGCCTGGGTGACA TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGGGATTGCGCCACTGCATTCCAGCCTGGGTGACA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1038202055 Functional Loss SNV dbSNP153 33..33 33 - - - 72235 RMVar_ID_72235 Human_SNP_ID_560853655 m1A Human chr14 + 74763921 74763921 74763921 GGGCCTCCTGGTTTGGTTCCAATGGAGCTGGAATCCCCCCCTGAATCTCCCCCTGTGCCGCCTGG GGGCCTCCTGGTTTGGTTCCAATGGAGCTGGACTCCCCCCCTGAATCTCCCCCTGTGCCGCCTGG A C YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:74763766..74764200 26863196 MeRIP-seq:(Medium) rs760709881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757610,Human_RBP_ID_8410119,Human_RBP_ID_17076688,Human_RBP_ID_17687614,Human_RBP_ID_18936889,Human_RBP_ID_22045301 72236 RMVar_ID_72236 Human_SNP_ID_560853705 m1A Human chr14 + 74763982 74763982 74763982 CTGGGTCCTATATGCCCCCATCTCAGTCTTACATGCCCCCACCTCAGCCGCCACCCTCTTACTAC CTGGGTCCTATATGCCCCCATCTCAGTCTTACCTGCCCCCACCTCAGCCGCCACCCTCTTACTAC A C YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74763937..74764176 26863196 MeRIP-seq:(Medium) rs765397089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9323815,Human_RBP_ID_17076481,Human_RBP_ID_18936890,Human_RBP_ID_22045301,Human_RBP_ID_22188625,Human_RBP_ID_22925166 72237 RMVar_ID_72237 Human_SNP_ID_560853706 m1A Human chr14 + 74763982 74763982 74763982 CTGGGTCCTATATGCCCCCATCTCAGTCTTACATGCCCCCACCTCAGCCGCCACCCTCTTACTAC CTGGGTCCTATATGCCCCCATCTCAGTCTTACGTGCCCCCACCTCAGCCGCCACCCTCTTACTAC A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74763937..74764176 26863196 MeRIP-seq:(Medium) rs765397089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9323815,Human_RBP_ID_17076481,Human_RBP_ID_18936890,Human_RBP_ID_22045301,Human_RBP_ID_22188625,Human_RBP_ID_22925166 72238 RMVar_ID_72238 Human_SNP_ID_560853714 m1A Human chr14 + 74763990 74763990 74763990 TATATGCCCCCATCTCAGTCTTACATGCCCCCACCTCAGCCGCCACCCTCTTACTACCCCCCGAC TATATGCCCCCATCTCAGTCTTACATGCCCCCTCCTCAGCCGCCACCCTCTTACTACCCCCCGAC A T YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:74763896..74764105 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9323815,Human_RBP_ID_17076481,Human_RBP_ID_18936890,Human_RBP_ID_22045301,Human_RBP_ID_22188625,Human_RBP_ID_22925166 72239 RMVar_ID_72239 Human_SNP_ID_560853719 m1A Human chr14 - 74763993 74763993 74763993 GAGGTCGGGGGGTAGTAAGAGGGTGGCGGCTGAGGTGGGGGCATGTAAGACTGAGATGGGGGCAT GAGGTCGGGGGGTAGTAAGAGGGTGGCGGCTGTGGTGGGGGCATGTAAGACTGAGATGGGGGCAT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:74763911..74764100 26863196 MeRIP-seq:(Medium) rs1287898174 Functional Loss SNV dbSNP153 33..33 33 - - - 72240 RMVar_ID_72240 Human_SNP_ID_560857626 m1A Human chr14 + 74778668 74778668 74778668 CCTCCAAATGAGGAAGTGCCACCTCCTCTCCCACCTGAGGAACCCCAGGTAACCATATAATTAAT CCTCCAAATGAGGAAGTGCCACCTCCTCTCCCGCCTGAGGAACCCCAGGTAACCATATAATTAAT A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74778547..74780469 32194978 MeRIP-seq:(Medium) rs779311854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757048,Human_RBP_ID_5522815,Human_RBP_ID_9369189,Human_RBP_ID_27808426 Human_Splice_Rec_1536209,Human_Splice_Rec_1536247 RMVar_hsa_circ_45050,RMVar_hsa_circ_304151,RMVar_hsa_circ_349439,RMVar_hsa_circ_65639,RMVar_hsa_circ_167941 72241 RMVar_ID_72241 Human_SNP_ID_560858517 m1A Human chr14 + 74781921 74781921 74781921 CCACCTGTCATGCCCCTCCCACCATTGTCTTCAGCTACACCTCCTCCAGGAATACCTCCCCCTGG CCACCTGTCATGCCCCTCCCACCATTGTCTTCGGCTACACCTCCTCCAGGAATACCTCCCCCTGG A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:74781712..74781950 26863196 MeRIP-seq:(Medium) rs192608859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757049,Human_RBP_ID_1499264,Human_RBP_ID_8410131,Human_RBP_ID_17247917,Human_RBP_ID_17363522,Human_RBP_ID_22044841 RMVar_hsa_circ_45050,RMVar_hsa_circ_349439,RMVar_hsa_circ_167943,RMVar_hsa_circ_110747,RMVar_hsa_circ_323259,RMVar_hsa_circ_293593,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_167942 72242 RMVar_ID_72242 Human_SNP_ID_560858518 m1A Human chr14 + 74781921 74781921 74781921 CCACCTGTCATGCCCCTCCCACCATTGTCTTCAGCTACACCTCCTCCAGGAATACCTCCCCCTGG CCACCTGTCATGCCCCTCCCACCATTGTCTTCTGCTACACCTCCTCCAGGAATACCTCCCCCTGG A T YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:74781712..74781950 26863196 MeRIP-seq:(Medium) rs192608859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757049,Human_RBP_ID_1499264,Human_RBP_ID_8410131,Human_RBP_ID_17247917,Human_RBP_ID_17363522,Human_RBP_ID_22044841 RMVar_hsa_circ_45050,RMVar_hsa_circ_349439,RMVar_hsa_circ_167943,RMVar_hsa_circ_110747,RMVar_hsa_circ_323259,RMVar_hsa_circ_293593,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_167942 72243 RMVar_ID_72243 Human_SNP_ID_560862565 m1A Human chr14 - 74798479 74798479 74798479 TCTTCTCTCGACTATCTTCTCTTCTACCCATCATCTTATCCCGAAAGTCTTCTTGCTTGACCAAT TCTTCTCTCGACTATCTTCTCTTCTACCCATCGTCTTATCCCGAAAGTCTTCTTGCTTGACCAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74798368..74798518 32194978 MeRIP-seq:(Medium) rs781302040 Functional Loss SNV dbSNP153 33..33 33 - - - 72244 RMVar_ID_72244 Human_SNP_ID_560862585 m1A Human chr14 + 74798536 74798536 74798536 AGAGAAGATGAACAGAGGAGAAGGTAGCCGGGACAGAGGGTTGGTGAGGCCTGGAAGCAGTCGGG AGAGAAGATGAACAGAGGAGAAGGTAGCCGGGGCAGAGGGTTGGTGAGGCCTGGAAGCAGTCGGG A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:74798335..74798819;chr14:74798351..74798826 26863196 MeRIP-seq:(Medium) rs770551279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4282,Human_RBP_ID_39526,Human_RBP_ID_5463745,Human_RBP_ID_5522825,Human_RBP_ID_6384636,Human_RBP_ID_8796229,Human_RBP_ID_9369194,Human_RBP_ID_18411038,Human_RBP_ID_22044617,Human_RBP_ID_22926285,Human_RBP_ID_24543716,Human_RBP_ID_26325242 RMVar_hsa_circ_45050,RMVar_hsa_circ_167943,RMVar_hsa_circ_110747,RMVar_hsa_circ_293593,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_332025,RMVar_hsa_circ_167942,RMVar_hsa_circ_353308,RMVar_hsa_circ_167945 72245 RMVar_ID_72245 Human_SNP_ID_560862634 m1A Human chr14 + 74798659 74798659 74798659 AAGGGGACCACCTCGGAGGGCTGGCAGTCAGGAGAGGGGACCTCTTCGAAGGGCTGGGAGTAGAG AAGGGGACCACCTCGGAGGGCTGGCAGTCAGGGGAGGGGACCTCTTCGAAGGGCTGGGAGTAGAG A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:74798436..74798700 26863196 MeRIP-seq:(Medium) rs1204006403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231122,Human_RBP_ID_756544,Human_RBP_ID_813083,Human_RBP_ID_6384639,Human_RBP_ID_22044618,Human_RBP_ID_22438786,Human_RBP_ID_26325243,Human_RBP_ID_26768637 RMVar_hsa_circ_45050,RMVar_hsa_circ_167943,RMVar_hsa_circ_110747,RMVar_hsa_circ_293593,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_332025,RMVar_hsa_circ_167942,RMVar_hsa_circ_353308,RMVar_hsa_circ_167945 72246 RMVar_ID_72246 Human_SNP_ID_560865446 m1A Human chr14 - 74809526 74809523 74809526 GAAGTTTGTGGCTTTATCACTGGAGGAGGAGGAGGTAGAGGTGGAGGAGGTGGAGGTGGTGGTAT GAAGTTTGTGGCTTTATCACTGGAGGAGGAGG___TAGAGGTGGAGGAGGTGGAGGTGGTGGTAT ACCT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74809426..74809938 32194978 MeRIP-seq:(Medium) rs773250816 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_167948 72247 RMVar_ID_72247 Human_SNP_ID_560867673 m1A Human chr14 + 74818296 74818296 74818296 ATGATGCGTCTAGATATTCGTTCTTTGCTGCAAGATGCTGCTATTGAAGAGGTGAGTATCCTTTG ATGATGCGTCTAGATATTCGTTCTTTGCTGCAGGATGCTGCTATTGAAGAGGTGAGTATCCTTTG A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74818250..74821093 32194978 MeRIP-seq:(Medium) rs1180540945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39539,Human_RBP_ID_1824410,Human_RBP_ID_3461514,Human_RBP_ID_9369206,Human_RBP_ID_18979783,Human_RBP_ID_27808442 Human_Splice_Rec_1536234,Human_Splice_Rec_1536235,Human_Splice_Rec_1536270,Human_Splice_Rec_1536271,Human_Splice_Rec_1536304,Human_Splice_Rec_1536305,Human_Splice_Rec_1536330,Human_Splice_Rec_1536331,Human_Splice_Rec_1536334,Human_Splice_Rec_1536335,Human_Splice_Rec_1536339 Human_miRNA_ID_363787,Human_miRNA_ID_371002,Human_miRNA_ID_378175,Human_miRNA_ID_1238776,Human_miRNA_ID_1454539,Human_miRNA_ID_1937890,Human_miRNA_ID_1948990,Human_miRNA_ID_2101241,Human_miRNA_ID_2107195,Human_miRNA_ID_2113139,Human_miRNA_ID_2596933,Human_miRNA_ID_2650229,Human_miRNA_ID_2652179,Human_miRNA_ID_2739842,Human_miRNA_ID_3040440 RMVar_hsa_circ_8535,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_357377,RMVar_hsa_circ_72065,RMVar_hsa_circ_350698,RMVar_hsa_circ_318406,RMVar_hsa_circ_17700,RMVar_hsa_circ_167946,RMVar_hsa_circ_44316,RMVar_hsa_circ_44818,RMVar_hsa_circ_45930,RMVar_hsa_circ_266086,RMVar_hsa_circ_33547,RMVar_hsa_circ_17049,RMVar_hsa_circ_27138 72248 RMVar_ID_72248 Human_SNP_ID_560882686 m1A Human chr14 - 74881996 74881996 74881996 GCCAGACCGTACCTTCTGGAAGGCGGAGAGCGAGCGGCTGAACGCCCGAGACACACAGCGGGATC GCCAGACCGTACCTTCTGGAAGGCGGAGAGCGGGCGGCTGAACGCCCGAGACACACAGCGGGATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:74881948..74882062 26863196 MeRIP-seq:(Medium) rs1328895665 Functional Loss SNV dbSNP153 33..33 33 - - - 72249 RMVar_ID_72249 Human_SNP_ID_560883655 m1A Human chr14 + 74885535 74885535 74885535 GGGTGAGCAGACCTTTTCCATTCCCAGCATGTATCCTTTGTGAGATAAGAGTTGTTGGTTAAGAG GGGTGAGCAGACCTTTTCCATTCCCAGCATGTGTCCTTTGTGAGATAAGAGTTGTTGGTTAAGAG A G DLST Ensembl:ENSG00000119689 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:74885532..74885607 26863196 MeRIP-seq:(Medium) rs1244633160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6385069 Human_Splice_Rec_1536377,Human_Splice_Rec_1536387,Human_Splice_Rec_1536401,Human_Splice_Rec_1536407,Human_Splice_Rec_1536429,Human_Splice_Rec_1536441,Human_Splice_Rec_1536467,Human_Splice_Rec_1536495,Human_Splice_Rec_1536509,Human_Splice_Rec_1536579 RMVar_hsa_circ_33081 72250 RMVar_ID_72250 Human_SNP_ID_560898432 m1A Human chr14 - 74942086 74942086 74942086 TTGCTTGTACTGGGACATTGTTCTTTCCGGCCAAGGTGCCACCACCCTGCCCCCCCTAAGAGACA TTGCTTGTACTGGGACATTGTTCTTTCCGGCCGAGGTGCCACCACCCTGCCCCCCCTAAGAGACA T C PGF Ensembl:ENSG00000119630 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451878,Human_RBP_ID_5112726,Human_RBP_ID_27559167 GWAS_ID_8842,GWAS_ID_8843,GWAS_ID_8844,GWAS_ID_8845,GWAS_ID_8846,GWAS_ID_8847,GWAS_ID_8848 72251 RMVar_ID_72251 Human_SNP_ID_560899673 m1A Human chr14 + 74946429 74946429 74946429 TCCCGCAGAGGCCTAGGGAAACAGACAGAGAGAGGGGCAGAGGAACGTTAGGAAAGCAATAAGTG TCCCGCAGAGGCCTAGGGAAACAGACAGAGAGTGGGGCAGAGGAACGTTAGGAAAGCAATAAGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:74946427..74946506 26863196 MeRIP-seq:(Medium) rs1180604936 Functional Loss SNV dbSNP153 33..33 33 - - - 72252 RMVar_ID_72252 Human_SNP_ID_560901942 m1A Human chr14 - 74955436 74955436 74955436 CGCCGGGCCGCTCCCCGTCGGGTTCCCCAGCCACAGCCTTACCTACGGGCTCCTGACTCCGCAAG CGCCGGGCCGCTCCCCGTCGGGTTCCCCAGCCGCAGCCTTACCTACGGGCTCCTGACTCCGCAAG T C PGF Ensembl:ENSG00000119630 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74955386..74955486 32194978 MeRIP-seq:(Medium) rs1216420484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5493895,Human_RBP_ID_27432893 72253 RMVar_ID_72253 Human_SNP_ID_294064868 m1A Human chr6 + 120262375 120262375 120262375 CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGAAGGGCCAGCGCCATTCCAATGGAATGGCTTTTT CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGACGGGCCAGCGCCATTCCAATGGAATGGCTTTTT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:120262326..120262400 26863196 MeRIP-seq:(Medium) rs200378569 Functional Loss SNV dbSNP153 33..33 33 - - - 72254 RMVar_ID_72254 Human_SNP_ID_294064869 m1A Human chr6 + 120262375 120262375 120262375 CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGAAGGGCCAGCGCCATTCCAATGGAATGGCTTTTT CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGATGGGCCAGCGCCATTCCAATGGAATGGCTTTTT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:120262326..120262400 26863196 MeRIP-seq:(Medium) rs200378569 Functional Loss SNV dbSNP153 33..33 33 - - - 72255 RMVar_ID_72255 Human_SNP_ID_294294597 m1A Human chr6 + 121190266 121190266 121190266 AGTTCCAACCTCCCTCCTTCCCCCTCCACCTCATCCTTTCCTCATTCCCCCTCCACCTTATCCTT AGTTCCAACCTCCCTCCTTCCCCCTCCACCTCCTCCTTTCCTCATTCCCCCTCCACCTTATCCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:121190062..121190303 26863196 MeRIP-seq:(Medium) rs1328368825 Functional Loss SNV dbSNP153 33..33 33 - - - 72256 RMVar_ID_72256 Human_SNP_ID_294593643 m1A Human chr6 - 122437175 122437167 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACA________TGTGTACAAAATCAAATACATTGTT ATATATTTT A Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1338639498 Functional Loss DEL dbSNP153 33..40 33 - - - 72257 RMVar_ID_72257 Human_SNP_ID_294593648 m1A Human chr6 - 122437175 122437171 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACA____TATATGTGTACAAAATCAAATACATTGTT ATTTT A Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58860296 Functional Loss DEL dbSNP153 33..36 33 - - - GWAS_ID_8849 72258 RMVar_ID_72258 Human_SNP_ID_294593649 m1A Human chr6 - 122437175 122437171 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACA__AATATATGTGTACAAAATCAAATACATTGTT ATTTT ATT Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58860296 Functional Loss DEL dbSNP153 33..34 33 - - - GWAS_ID_8849 72259 RMVar_ID_72259 Human_SNP_ID_294593650 m1A Human chr6 - 122437175 122437171 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACA_AAATATATGTGTACAAAATCAAATACATTGTT ATTTT ATTT Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58860296 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_8849 72260 RMVar_ID_72260 Human_SNP_ID_294593666 m1A Human chr6 - 122437175 122437175 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACACAAATATATGTGTACAAAATCAAATACATTGTT T G Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs546653 Functional Loss SNV dbSNP153 33..33 33 - - - 72261 RMVar_ID_72261 Human_SNP_ID_294602249 m1A Human chr6 + 122471769 122471769 122471769 TCTCCACAACGTCACAAGAGCAGCGGATACAGACAAGATGGAGACAGCTTCTTTCTCGCCTTTCC TCTCCACAACGTCACAAGAGCAGCGGATACAGTCAAGATGGAGACAGCTTCTTTCTCGCCTTTCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:122471722..122471800 26863196 MeRIP-seq:(Medium) rs1208259821 Functional Loss SNV dbSNP153 33..33 33 - - - 72262 RMVar_ID_72262 Human_SNP_ID_294602253 m1A Human chr6 - 122471775 122471775 122471775 AATCTCGGAAAGGCGAGAAAGAAGCTGTCTCCATCTTGTCTGTATCCGCTGCTCTTGTGACGTTG AATCTCGGAAAGGCGAGAAAGAAGCTGTCTCCGTCTTGTCTGTATCCGCTGCTCTTGTGACGTTG T C SERINC1 Ensembl:ENSG00000111897 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:122471659..122471800;chr6:122471640..122471800 26863196 MeRIP-seq:(Medium) rs1210752201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4863122,Human_RBP_ID_18852899,Human_RBP_ID_23067430,Human_RBP_ID_24132569 Human_Splice_Rec_806363 Human_miRNA_ID_2438210,Human_miRNA_ID_2756302 RMVar_hsa_circ_107999,RMVar_hsa_circ_241255,RMVar_hsa_circ_241257 72263 RMVar_ID_72263 Human_SNP_ID_294676231 m1A Human chr6 - 122789329 122789329 122789329 GCGCACCAGCGCCATGGAGGGCCGCGGGGCTGACCTGGAGGTTCGGGCTGTCCCGCAGCTCCACT GCGCACCAGCGCCATGGAGGGCCGCGGGGCTGTCCTGGAGGTTCGGGCTGTCCCGCAGCTCCACT T A lnc-SERINC1-8,lnc-SERINC1-6 RNACentral:URS0000D5D293,RNACentral:URS0000D58F89 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:122789283..122789489 26863196 MeRIP-seq:(Medium) rs1302222934 Functional Loss SNV dbSNP153 33..33 33 - - - 72264 RMVar_ID_72264 Human_SNP_ID_295212569 m1A Human chr6 - 124962163 124962163 124962163 TGGGAGGAGACGGCCGTCAGTCCCGCGCCATCACCGGTCCCGGCTGCCGGACGCGCGGCCCGAGG TGGGAGGAGACGGCCGTCAGTCCCGCGCCATCGCCGGTCCCGGCTGCCGGACGCGCGGCCCGAGG T C RNF217-AS1 Ensembl:ENSG00000236548 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:124962072..124962166 26863410 MeRIP-seq:(Medium) rs1450467802 Functional Loss SNV dbSNP153 33..33 33 - - - 72265 RMVar_ID_72265 Human_SNP_ID_295212591 m1A Human chr6 - 124962247 124962247 124962247 GCTCTGGGCTCGGGCGCGCCCGCCCCACATGCAGCTCGGGGCGGCGCCGCAGCCCCAGCGAGCCC GCTCTGGGCTCGGGCGCGCCCGCCCCACATGCTGCTCGGGGCGGCGCCGCAGCCCCAGCGAGCCC T A RNF217-AS1 Ensembl:ENSG00000236548 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:124962197..124962316 32194978 MeRIP-seq:(Medium) rs1330198669 Functional Loss SNV dbSNP153 33..33 33 - - - 72266 RMVar_ID_72266 Human_SNP_ID_295216647 m1A Human chr6 + 124979430 124979430 124979430 GTGACCATGACTGGAAAGGGGTTTAGAAAGGCAGTGTGGCAAATACAGGTAGAGAGATGAGAGCG GTGACCATGACTGGAAAGGGGTTTAGAAAGGCGGTGTGGCAAATACAGGTAGAGAGATGAGAGCG A G RNF217 Ensembl:ENSG00000146373 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:124979333..124979593 26863196 MeRIP-seq:(Medium) rs1484867557 Functional Loss SNV dbSNP153 33..33 33 - - - 72267 RMVar_ID_72267 Human_SNP_ID_295216656 m1A Human chr6 + 124979492 124979490 124979492 GCGGAATGGTGACAGCAAGAGTCAGCAGAACAAAGATACCAGCGTGGCGCAGAGCACCAAAGGCA GCGGAATGGTGACAGCAAGAGTCAGCAGAAC__AGATACCAGCGTGGCGCAGAGCACCAAAGGCA CAA C RNF217 Ensembl:ENSG00000146373 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:124979352..124979616 26863196 MeRIP-seq:(Medium) rs1207937959 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15628652,Human_RBP_ID_18853236 72268 RMVar_ID_72268 Human_SNP_ID_295216658 m1A Human chr6 + 124979492 124979492 124979492 GCGGAATGGTGACAGCAAGAGTCAGCAGAACAAAGATACCAGCGTGGCGCAGAGCACCAAAGGCA GCGGAATGGTGACAGCAAGAGTCAGCAGAACACAGATACCAGCGTGGCGCAGAGCACCAAAGGCA A C RNF217 Ensembl:ENSG00000146373 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:124979352..124979616 26863196 MeRIP-seq:(Medium) rs1275066380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15628652,Human_RBP_ID_18853236 72269 RMVar_ID_72269 Human_SNP_ID_295227399 m1A Human chr6 - 125025876 125025876 125025876 ACAGTCAAAAACTTCACCTTGTACTTGACAGAATAAAAATCCAACAGGATCAGCTGAGAACACCT ACAGTCAAAAACTTCACCTTGTACTTGACAGACTAAAAATCCAACAGGATCAGCTGAGAACACCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:125025870..125026044 26863196 MeRIP-seq:(Medium) rs1264103157 Functional Loss SNV dbSNP153 33..33 33 - - - 72270 RMVar_ID_72270 Human_SNP_ID_295240982 m1A Human chr6 + 125083045 125083045 125083045 ATCTTGAAAAACACTGAGAGGAACCTTCTACCATCTCATCTCCCAGTGATTCTCCGTGGGCCACA ATCTTGAAAAACACTGAGAGGAACCTTCTACCGTCTCATCTCCCAGTGATTCTCCGTGGGCCACA A G RNF217 Ensembl:ENSG00000146373 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:125083003..125083116 26863196 MeRIP-seq:(Medium) rs994018347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5510391,Human_RBP_ID_17418024,Human_RBP_ID_18062917,Human_RBP_ID_26828764 72271 RMVar_ID_72271 Human_SNP_ID_295257824 m1A Human chr6 + 125153940 125153940 125153940 AGCACCAGGGTGTCCCCGCCGCCCTCAGCTCGAAGTCAGCCACCATGGAGGCGCAGGCACAAGGT AGCACCAGGGTGTCCCCGCCGCCCTCAGCTCGGAGTCAGCCACCATGGAGGCGCAGGCACAAGGT A G TPD52L1 Ensembl:ENSG00000111907 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:125153778..125154018 26863196 MeRIP-seq:(Medium) rs1300693156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904242,Human_RBP_ID_9336294 Human_Splice_Rec_807139,Human_Splice_Rec_807153,Human_Splice_Rec_807163,Human_Splice_Rec_807171,Human_Splice_Rec_807183,Human_Splice_Rec_807193,Human_Splice_Rec_807199 RMVar_hsa_circ_241296,RMVar_hsa_circ_114276 72272 RMVar_ID_72272 Human_SNP_ID_295273616 m1A Human chr6 + 125220168 125220168 125220168 CTTCTCTAGCATGCTCTCTGAGGAGGAAAAGGAAGAGTTAAAAGCAGAGTTAGTTCAGGTATGTT CTTCTCTAGCATGCTCTCTGAGGAGGAAAAGGTAGAGTTAAAAGCAGAGTTAGTTCAGGTATGTT A T TPD52L1 Ensembl:ENSG00000111907 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:125220016..125220200 26863196 MeRIP-seq:(Medium) rs1292199712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904243,Human_RBP_ID_18413883,Human_RBP_ID_22105387 Human_Splice_Rec_807134,Human_Splice_Rec_807135,Human_Splice_Rec_807140,Human_Splice_Rec_807141,Human_Splice_Rec_807154,Human_Splice_Rec_807155,Human_Splice_Rec_807164,Human_Splice_Rec_807165,Human_Splice_Rec_807172,Human_Splice_Rec_807173,Human_Splice_Rec_807184,Human_Splice_Rec_807185,Human_Splice_Rec_807194,Human_Splice_Rec_807195,Human_Splice_Rec_807200,Human_Splice_Rec_807201,Human_Splice_Rec_807212,Human_Splice_Rec_807213,Human_Splice_Rec_807220,Human_Splice_Rec_807221,Human_Splice_Rec_807232,Human_Splice_Rec_807233,Human_Splice_Rec_807240,Human_Splice_Rec_807241,Human_Splice_Rec_807247 RMVar_hsa_circ_241296,RMVar_hsa_circ_114276,RMVar_hsa_circ_117642,RMVar_hsa_circ_359181,RMVar_hsa_circ_45463,RMVar_hsa_circ_241299 72273 RMVar_ID_72273 Human_SNP_ID_295273618 m1A Human chr6 + 125220181 125220181 125220181 CTCTCTGAGGAGGAAAAGGAAGAGTTAAAAGCAGAGTTAGTTCAGGTATGTTTAGTAATCTTATT CTCTCTGAGGAGGAAAAGGAAGAGTTAAAAGCGGAGTTAGTTCAGGTATGTTTAGTAATCTTATT A G TPD52L1 Ensembl:ENSG00000111907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:125220033..125229072 26863196 MeRIP-seq:(Medium) rs1006192509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18413883,Human_RBP_ID_22105387 Human_Splice_Rec_807135,Human_Splice_Rec_807141,Human_Splice_Rec_807155,Human_Splice_Rec_807165,Human_Splice_Rec_807173,Human_Splice_Rec_807185,Human_Splice_Rec_807195,Human_Splice_Rec_807201,Human_Splice_Rec_807213,Human_Splice_Rec_807221,Human_Splice_Rec_807233,Human_Splice_Rec_807241,Human_Splice_Rec_807247 Human_miRNA_ID_2659345,Human_miRNA_ID_2659346 RMVar_hsa_circ_241296,RMVar_hsa_circ_114276,RMVar_hsa_circ_117642,RMVar_hsa_circ_359181,RMVar_hsa_circ_45463,RMVar_hsa_circ_241299 72274 RMVar_ID_72274 Human_SNP_ID_295275598 m1A Human chr6 - 125229106 125229105 125229106 TGTTGTAATTTCGTCTTCTAGCTACAAGGCGGAGGGGAAATGGTGGGGGAAAATGTCAGACCAGC TGTTGTAATTTCGTCTTCTAGCTACAAGGCGG_GGGGAAATGGTGGGGGAAAATGTCAGACCAGC CT C HDDC2 Ensembl:ENSG00000111906 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:125229101..125229150 26863196 MeRIP-seq:(Medium) rs780669983 Functional Loss DEL dbSNP153 33..33 33 - - - 72275 RMVar_ID_72275 Human_SNP_ID_295292689 m1A Human chr6 + 125300627 125300627 125300627 ATGTGATCTGAAACGCTCTCCGGCCTCTGGACATTTCTGTATACCCAGCCAGTTCGTGGGACTCT ATGTGATCTGAAACGCTCTCCGGCCTCTGGACTTTTCTGTATACCCAGCCAGTTCGTGGGACTCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:125300576..125300713 26863196 MeRIP-seq:(Medium) rs1373607502 Functional Loss SNV dbSNP153 33..33 33 - - - 72276 RMVar_ID_72276 Human_SNP_ID_295292697 m1A Human chr6 - 125300648 125300648 125300648 TTTCTTCTTCATATTTATCAGAGAGTCCCACGAACTGGCTGGGTATACAGAAATGTCCAGAGGCC TTTCTTCTTCATATTTATCAGAGAGTCCCACGGACTGGCTGGGTATACAGAAATGTCCAGAGGCC T C HDDC2 Ensembl:ENSG00000111906 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:125300599..125300682 26863196 MeRIP-seq:(Medium) rs1480646458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_652639,Human_RBP_ID_4904245,Human_RBP_ID_5090342,Human_RBP_ID_7533354,Human_RBP_ID_9336295,Human_RBP_ID_9401057,Human_RBP_ID_17663812,Human_RBP_ID_22684401,Human_RBP_ID_26040555,Human_RBP_ID_26353248 Human_Splice_Rec_807276,Human_Splice_Rec_807286,Human_Splice_Rec_807296,Human_Splice_Rec_807304,Human_Splice_Rec_807312,Human_Splice_Rec_807320,Human_Splice_Rec_807326 RMVar_hsa_circ_241301,RMVar_hsa_circ_343778,RMVar_hsa_circ_293665 72277 RMVar_ID_72277 Human_SNP_ID_295293315 m1A Human chr6 - 125302002 125302002 125302002 GAGTAAGAGGAGGGGGAAGAAAGACAAGGGGAAGGGGAGGAGGAGGAGGACGGGGAGGAGCTTCG GAGTAAGAGGAGGGGGAAGAAAGACAAGGGGAGGGGGAGGAGGAGGAGGACGGGGAGGAGCTTCG T C HDDC2 Ensembl:ENSG00000111906 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1310679184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13536,Human_RBP_ID_947876,Human_RBP_ID_5152237,Human_RBP_ID_5327217,Human_RBP_ID_8944034,Human_RBP_ID_9437884,Human_RBP_ID_22462883,Human_RBP_ID_26355539 72278 RMVar_ID_72278 Human_SNP_ID_295293354 m1A Human chr6 - 125302087 125302073 125302088 GGAGGAGTTGGAAGGGGAGGAGGAAGAGGGGGAGCAGGAAGAGGGGCAGAAGGAAGAAGAAGAGG GGAGGAGTTGGAAGGGGAGGAGGAAGAGGGG_______________CAGAAGGAAGAAGAAGAGG GCCCCTCTTCCTGCTC G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:125301961..125302098 26863196 MeRIP-seq:(Medium) rs1210306600 Functional Loss DEL dbSNP153 32..46 33 - - - 72279 RMVar_ID_72279 Human_SNP_ID_295293357 m1A Human chr6 - 125302084 125302082 125302085 GGAGTTGGAAGGGGAGGAGGAAGAGGGGGAGCAGGAAGAGGGGCAGAAGGAAGAAGAAGAGGGGG GGAGTTGGAAGGGGAGGAGGAAGAGGGGGAG___GAAGAGGGGCAGAAGGAAGAAGAAGAGGGGG CCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:125301822..125302125 26863196 MeRIP-seq:(Medium) rs1449014310 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_26042466 72280 RMVar_ID_72280 Human_SNP_ID_295394817 m1A Human chr6 + 125749682 125749682 125749682 AGACCGCGCCGCCGCCGGAGCCGCGCCTGCCCAGGCCCGGGGAGGGAGGAGGCGGGCGTCAGGGT AGACCGCGCCGCCGCCGGAGCCGCGCCTGCCCGGGCCCGGGGAGGGAGGAGGCGGGCGTCAGGGT A G HEY2 Ensembl:ENSG00000135547 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:125749631..125752033 26863196 MeRIP-seq:(Medium) rs1204195464 Functional Loss SNV dbSNP153 33..33 33 - - - 72281 RMVar_ID_72281 Human_SNP_ID_295403090 m1A Human chr6 - 125780262 125780262 125780262 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAAGTCTTGTTTTTCTTGAC TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGGTTCCCGGTCAGGGAAGTCTTGTTTTTCTTGAC T C tRNA-Glu-CTC-1-1,tRNA-Glu-CTC-2-1,lnc-HDDC2-15,lnc-HDDC2-11 RNACentral:URS00004F0321,RNACentral:URS0000635088,RNACentral:URS0000D5DBE7,RNACentral:URS0000D588CB tRNA,tRNA,lincRNA,lincRNA exon,exon,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs769352704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_652650,Human_RBP_ID_1393355,Human_RBP_ID_1663517,Human_RBP_ID_2007328,Human_RBP_ID_3791639,Human_RBP_ID_4863422,Human_RBP_ID_5268003,Human_RBP_ID_5276881,Human_RBP_ID_8629598,Human_RBP_ID_15629603,Human_RBP_ID_17092151,Human_RBP_ID_18853349,Human_RBP_ID_21219655,Human_RBP_ID_23120444,Human_RBP_ID_23137547,Human_RBP_ID_24133006,Human_RBP_ID_26709910,Human_RBP_ID_27102611,Human_RBP_ID_27519275,Human_RBP_ID_27749107 72282 RMVar_ID_72282 Human_SNP_ID_295450348 m1A Human chr6 - 125986558 125986558 125986558 TGAGGAGCAGATACCTGTTAAGGGTACACGACAGCGCCATTGCAGCTGCCCACCGTGCGCCTGCG TGAGGAGCAGATACCTGTTAAGGGTACACGACGGCGCCATTGCAGCTGCCCACCGTGCGCCTGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:125986508..125986919 26863196 MeRIP-seq:(Medium) rs1175684817 Functional Loss SNV dbSNP153 33..33 33 - - - 72283 RMVar_ID_72283 Human_SNP_ID_295450442 m1A Human chr6 - 125986715 125986715 125986715 CCCGCGCAGACCAGCGAAGACCCCCGAATCCCAGCTTCCTCGGGCTATGCAGATCACCTCCACCC CCCGCGCAGACCAGCGAAGACCCCCGAATCCCCGCTTCCTCGGGCTATGCAGATCACCTCCACCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:125986529..125986968;chr6:125986509..125986919 26863196 MeRIP-seq:(Medium) rs748085578 Functional Loss SNV dbSNP153 33..33 33 - - - 72284 RMVar_ID_72284 Human_SNP_ID_295450742 m1A Human chr6 + 125987979 125987979 125987979 TTCTTCATATGAAAACTAGGAGCGGGGAAGAAATTACTCAAAGGATAAGGTCAAAAGAGTAGCGG TTCTTCATATGAAAACTAGGAGCGGGGAAGAAGTTACTCAAAGGATAAGGTCAAAAGAGTAGCGG A G TRMT11 Ensembl:ENSG00000066651 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:125987975..125988193 26863196 MeRIP-seq:(Medium) rs971178609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13212,Human_RBP_ID_9187092 RMVar_hsa_circ_112808,RMVar_hsa_circ_241323,RMVar_hsa_circ_118393,RMVar_hsa_circ_241325,RMVar_hsa_circ_91715,RMVar_hsa_circ_241326,RMVar_hsa_circ_241324 72285 RMVar_ID_72285 Human_SNP_ID_295450755 m1A Human chr6 - 125988024 125988024 125988024 CCGACTTTCCCTTAATATCAATGCTTCCAAGCATCTATACTTGGCCCGCTACTCTTTTGACCTTA CCGACTTTCCCTTAATATCAATGCTTCCAAGCGTCTATACTTGGCCCGCTACTCTTTTGACCTTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:125988022..125988109 26863196 MeRIP-seq:(Medium) rs1457786815 Functional Loss SNV dbSNP153 33..33 33 - - - 72286 RMVar_ID_72286 Human_SNP_ID_295465248 m1A Human chr6 + 126051308 126051308 126051308 GAGGAGGTAATGATGTGTGAGGCAGAGGACATAGCAAAGGAATAGAGAGCATGGTATGTAGGGAA GAGGAGGTAATGATGTGTGAGGCAGAGGACATTGCAAAGGAATAGAGAGCATGGTATGTAGGGAA A T TRMT11 Ensembl:ENSG00000066651 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:126051260..126051378 26863196 MeRIP-seq:(Medium) rs1368025839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7534631,Human_RBP_ID_15632048 RMVar_hsa_circ_58128,RMVar_hsa_circ_367595 72287 RMVar_ID_72287 Human_SNP_ID_295529589 m1A Human chr6 - 126340196 126340196 126340196 GTATCGCACACAAGCTCCGGGGACACTGGGCCAGCGAAAACAATCCGGTCCGTATGACGCTTCTT GTATCGCACACAAGCTCCGGGGACACTGGGCCGGCGAAAACAATCCGGTCCGTATGACGCTTCTT T C AL356534.1 Ensembl:ENSG00000286215 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:126340147..126340281 26863196 MeRIP-seq:(Medium) rs1275976678 Functional Loss SNV dbSNP153 33..33 33 - - - 72288 RMVar_ID_72288 Human_SNP_ID_295529594 m1A Human chr6 + 126340202 126340202 126340202 CGTCATACGGACCGGATTGTTTTCGCTGGCCCAGTGTCCCCGGAGCTTGTGTGCGATACAGAGAG CGTCATACGGACCGGATTGTTTTCGCTGGCCCGGTGTCCCCGGAGCTTGTGTGCGATACAGAGAG A G CENPW Ensembl:ENSG00000203760 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:126340151..126340225 32194978 MeRIP-seq:(Medium) rs916907796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_652776,Human_RBP_ID_1044376,Human_RBP_ID_1215056,Human_RBP_ID_1324501,Human_RBP_ID_4863635,Human_RBP_ID_5327539,Human_RBP_ID_5450448,Human_RBP_ID_5478752,Human_RBP_ID_5510416,Human_RBP_ID_7536564,Human_RBP_ID_8630282,Human_RBP_ID_9336297,Human_RBP_ID_9401071,Human_RBP_ID_15637756,Human_RBP_ID_22106145,Human_RBP_ID_22460805,Human_RBP_ID_22513211,Human_RBP_ID_24133507,Human_RBP_ID_27567900 Human_miRNA_ID_2661658,Human_miRNA_ID_2680105 RMVar_hsa_circ_241352,RMVar_hsa_circ_119445 72289 RMVar_ID_72289 Human_SNP_ID_295529628 m1A Human chr6 + 126340289 126340289 126340289 GGTACTTGACAGAGAGGATGGCGCTGTCGACCATAGTCTCCCAGAGGAAGCAGATAAAGCGGAAG GGTACTTGACAGAGAGGATGGCGCTGTCGACCGTAGTCTCCCAGAGGAAGCAGATAAAGCGGAAG A G CENPW Ensembl:ENSG00000203760 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:126340151..126340400 32194978 MeRIP-seq:(Medium) rs750494370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1324502,Human_RBP_ID_1663819,Human_RBP_ID_2008013,Human_RBP_ID_4905590,Human_RBP_ID_5478752,Human_RBP_ID_7536565,Human_RBP_ID_9336769,Human_RBP_ID_9401071,Human_RBP_ID_18063404,Human_RBP_ID_18853753,Human_RBP_ID_22462885,Human_RBP_ID_24133509,Human_RBP_ID_25961655 Human_miRNA_ID_937616,Human_miRNA_ID_957776,Human_miRNA_ID_2423809,Human_miRNA_ID_2433468,Human_miRNA_ID_2585549 RMVar_hsa_circ_241352,RMVar_hsa_circ_119445 72290 RMVar_ID_72290 Human_SNP_ID_295751274 m1A Human chr6 + 127287106 127287106 127287106 AATATAGGAGAAATGAACATGGACGTCGCAGGAAGATTAAGCGAGATATAATAGATATACCAAAG AATATAGGAGAAATGAACATGGACGTCGCAGGGAGATTAAGCGAGATATAATAGATATACCAAAG A G RNF146 Ensembl:ENSG00000118518 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:127286969..127287127 26863196 MeRIP-seq:(Medium) rs1405545969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241373 72291 RMVar_ID_72291 Human_SNP_ID_295758267 m1A Human chr6 - 127317038 127317038 127317038 AAAGCTTTTGAGGAGAGATTTTGGGATAAGGCAGAGGGCCAGATTACACTGGATTGAAGAAAGTA AAAGCTTTTGAGGAGAGATTTTGGGATAAGGCGGAGGGCCAGATTACACTGGATTGAAGAAAGTA T C ECHDC1 Ensembl:ENSG00000093144 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:127317031..127317273 26863196 MeRIP-seq:(Medium) rs1350770303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56935,RMVar_hsa_circ_350737,RMVar_hsa_circ_308499,RMVar_hsa_circ_92447,RMVar_hsa_circ_241375,RMVar_hsa_circ_241376 72292 RMVar_ID_72292 Human_SNP_ID_295764230 m1A Human chr6 - 127343438 127343437 127343438 AGAAGAGGAGAGGACCTACAAGAACGGAGGACAGGGGCGCACGATGGTCCCGGGGGGAGCGGAAA AGAAGAGGAGAGGACCTACAAGAACGGAGGAC_GGGGCGCACGATGGTCCCGGGGGGAGCGGAAA CT C ECHDC1 Ensembl:ENSG00000093144 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:127343380..127343467 26863410 MeRIP-seq:(Medium) rs1451261409 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3970440,Human_RBP_ID_4863759,Human_RBP_ID_9401077,Human_RBP_ID_26353253 72293 RMVar_ID_72293 Human_SNP_ID_295764234 m1A Human chr6 - 127343462 127343462 127343462 GGGATAGTAAAAGAGAAGACGCGGAGAAGAGGAGAGGACCTACAAGAACGGAGGACAGGGGCGCA GGGATAGTAAAAGAGAAGACGCGGAGAAGAGGCGAGGACCTACAAGAACGGAGGACAGGGGCGCA T G ECHDC1 Ensembl:ENSG00000093144 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:127343363..127343548 26863196 MeRIP-seq:(Medium) rs1416563660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9401077,Human_RBP_ID_26353253 72294 RMVar_ID_72294 Human_SNP_ID_295764249 m1A Human chr6 - 127343504 127343504 127343504 GGGGAACGGGATAAAGTTCCCGGAGAAAGGAAAGGAGAGCGTGGGATAGTAAAAGAGAAGACGCG GGGGAACGGGATAAAGTTCCCGGAGAAAGGAAGGGAGAGCGTGGGATAGTAAAAGAGAAGACGCG T C ECHDC1 Ensembl:ENSG00000093144 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:127343351..127343552 26863196 MeRIP-seq:(Medium) rs1312587333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26355543 72295 RMVar_ID_72295 Human_SNP_ID_295764250 m1A Human chr6 - 127343504 127343504 127343504 GGGGAACGGGATAAAGTTCCCGGAGAAAGGAAAGGAGAGCGTGGGATAGTAAAAGAGAAGACGCG GGGGAACGGGATAAAGTTCCCGGAGAAAGGAACGGAGAGCGTGGGATAGTAAAAGAGAAGACGCG T G ECHDC1 Ensembl:ENSG00000093144 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:127343351..127343552 26863196 MeRIP-seq:(Medium) rs1312587333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26355543 72296 RMVar_ID_72296 Human_SNP_ID_295975266 m1A Human chr6 + 128209043 128209043 128209043 CATTACACAATGCTTTAACAACATTGCTGCCTAATCTCTCATCCTTGACTCATTCTTTCTACCAT CATTACACAATGCTTTAACAACATTGCTGCCTGATCTCTCATCCTTGACTCATTCTTTCTACCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:128209041..128209130 26863196 MeRIP-seq:(Medium) rs1267440902 Functional Loss SNV dbSNP153 33..33 33 - - - 72297 RMVar_ID_72297 Human_SNP_ID_295996237 m1A Human chr6 - 128296128 128296125 128296128 AGTGAGCAAGAAGGGGAGAGGAGAAAGAGGAGAAGGAGGTTAAGACAGGGAGGGAATTGAGTCAG AGTGAGCAAGAAGGGGAGAGGAGAAAGAGGAG___GAGGTTAAGACAGGGAGGGAATTGAGTCAG CCTT C PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:128296126..128296225 26863196 MeRIP-seq:(Medium) rs1238372417 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_840305,Human_RBP_ID_17069825,Human_RBP_ID_17164801,Human_RBP_ID_25962539 RMVar_hsa_circ_6721,RMVar_hsa_circ_113780,RMVar_hsa_circ_241387,RMVar_hsa_circ_241392,RMVar_hsa_circ_98718,RMVar_hsa_circ_98736,RMVar_hsa_circ_74630,RMVar_hsa_circ_241396,RMVar_hsa_circ_127784,RMVar_hsa_circ_241410,RMVar_hsa_circ_241411,RMVar_hsa_circ_92294,RMVar_hsa_circ_241424,RMVar_hsa_circ_278007,RMVar_hsa_circ_273885,RMVar_hsa_circ_241414,RMVar_hsa_circ_241420,RMVar_hsa_circ_241422,RMVar_hsa_circ_303443,RMVar_hsa_circ_312732,RMVar_hsa_circ_241421,RMVar_hsa_circ_315874,RMVar_hsa_circ_344792,RMVar_hsa_circ_241425 72298 RMVar_ID_72298 Human_SNP_ID_296044142 m1A Human chr6 - 128495531 128495525 128495531 TGGAGCATGCTAGTAGATTTGTGGGGACTTAGAGAGAGGGAAGGATGAGAGATGCTGCCTGAGTA TGGAGCATGCTAGTAGATTTGTGGGGACTTAG______GGAAGGATGAGAGATGCTGCCTGAGTA CCTCTCT C PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:128495529..128495655 26863196 MeRIP-seq:(Medium) rs994781604 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_7539315,Human_RBP_ID_15642664 RMVar_hsa_circ_98736,RMVar_hsa_circ_241396 72299 RMVar_ID_72299 Human_SNP_ID_296044143 m1A Human chr6 - 128495531 128495525 128495531 TGGAGCATGCTAGTAGATTTGTGGGGACTTAGAGAGAGGGAAGGATGAGAGATGCTGCCTGAGTA TGGAGCATGCTAGTAGATTTGTGGGGACTTAG____AGGGAAGGATGAGAGATGCTGCCTGAGTA CCTCTCT CCT PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:128495529..128495655 26863196 MeRIP-seq:(Medium) rs994781604 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_7539315,Human_RBP_ID_15642664 RMVar_hsa_circ_98736,RMVar_hsa_circ_241396 72300 RMVar_ID_72300 Human_SNP_ID_296044144 m1A Human chr6 - 128495531 128495525 128495531 TGGAGCATGCTAGTAGATTTGTGGGGACTTAGAGAGAGGGAAGGATGAGAGATGCTGCCTGAGTA TGGAGCATGCTAGTAGATTTGTGGGGACTTAG__AGAGGGAAGGATGAGAGATGCTGCCTGAGTA CCTCTCT CCTCT PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:128495529..128495655 26863196 MeRIP-seq:(Medium) rs994781604 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7539315,Human_RBP_ID_15642664 RMVar_hsa_circ_98736,RMVar_hsa_circ_241396 72301 RMVar_ID_72301 Human_SNP_ID_296064857 m1A Human chr6 + 128580162 128580162 128580162 CTGCGATGTCGACACTCTGCACATGCTCCTCAAACTTGGTGATCTCCTCCTCCAGCAAGTCTGTC CTGCGATGTCGACACTCTGCACATGCTCCTCAGACTTGGTGATCTCCTCCTCCAGCAAGTCTGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:128580091..128580204 26863196 MeRIP-seq:(Medium) rs796418862 Functional Loss SNV dbSNP153 33..33 33 - - - 72302 RMVar_ID_72302 Human_SNP_ID_296332233 m1A Human chr6 + 129660411 129660411 129660411 CTGGGTGACCAATTAGATAAAGTAGATGAAGGAAACAGAAGAAACAAAGATGATTCCACAGTTTG CTGGGTGACCAATTAGATAAAGTAGATGAAGGCAACAGAAGAAACAAAGATGATTCCACAGTTTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:129660408..129660491;chr6:129660408..129660499 26863196 MeRIP-seq:(Medium) rs934968532 Functional Loss SNV dbSNP153 33..33 33 - - - 72303 RMVar_ID_72303 Human_SNP_ID_296335035 m1A Human chr6 + 129672143 129672143 129672143 TTCCTCTCCCCTTTCTTCTACTCCTGGCTCAGATTTTTCATCTATGTCCTCTGCAATCATCGCCA TTCCTCTCCCCTTTCTTCTACTCCTGGCTCAGGTTTTTCATCTATGTCCTCTGCAATCATCGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:129672141..129672306 26863196 MeRIP-seq:(Medium) rs952013760 Functional Loss SNV dbSNP153 33..33 33 - - - 72304 RMVar_ID_72304 Human_SNP_ID_296418811 m1A Human chr6 + 130020281 130020281 130020281 AGAGGCCGGCGGGGGTGGGGATCGGGAAGCGCAGGAGCCGAGGCATCCGCCGCGCGCCCCGCGAG AGAGGCCGGCGGGGGTGGGGATCGGGAAGCGCGGGAGCCGAGGCATCCGCCGCGCGCCCCGCGAG A G L3MBTL3 Ensembl:ENSG00000198945 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:130020267..130020381 26863196 MeRIP-seq:(Medium) rs1390337612 Functional Loss SNV dbSNP153 33..33 33 - - - 72305 RMVar_ID_72305 Human_SNP_ID_296418826 m1A Human chr6 - 130020323 130020323 130020323 TCAAGTTTTTCTCCCCGCCCGGCGGCCCCCACACTCCACCAGCTCGCGGGGCGCGCGGCGGATGC TCAAGTTTTTCTCCCCGCCCGGCGGCCCCCACCCTCCACCAGCTCGCGGGGCGCGCGGCGGATGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:130020285..130020369 26863196 MeRIP-seq:(Medium) rs1209132915 Functional Loss SNV dbSNP153 33..33 33 - - - 72306 RMVar_ID_72306 Human_SNP_ID_296618513 m1A Human chr6 - 130840079 130840079 130840079 TTCAAATTGCAGCAAATATACTGTATGAGAAAATATTAATACAGATTAAAAGCCTTTCTTACATC TTCAAATTGCAGCAAATATACTGTATGAGAAAGTATTAATACAGATTAAAAGCCTTTCTTACATC T C EPB41L2 Ensembl:ENSG00000079819 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:130840044..130840194 32194978 MeRIP-seq:(Medium) rs1192062932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_653077,Human_RBP_ID_2008385,Human_RBP_ID_18365711,Human_RBP_ID_25963142 72307 RMVar_ID_72307 Human_SNP_ID_296618610 m1A Human chr6 + 130840587 130840587 130840587 CTTCAGGGGTTCACAAAGTTGAGTGTTGTTTAAAAAATGACTTTCTAGAAGAGAAAAAAAAAAAA CTTCAGGGGTTCACAAAGTTGAGTGTTGTTTAGAAAATGACTTTCTAGAAGAGAAAAAAAAAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:130840493..130840593 32194978 MeRIP-seq:(Medium) rs1395962449 Functional Loss SNV dbSNP153 33..33 33 - - - 72308 RMVar_ID_72308 Human_SNP_ID_296625854 m1A Human chr6 - 130869974 130869974 130869974 GAGATTCGTAAGGTGGAGCCTGTGACACAAAAAGACTCCACCTCCCTGTCTTCTGAGAGCAGCAG GAGATTCGTAAGGTGGAGCCTGTGACACAAAAGGACTCCACCTCCCTGTCTTCTGAGAGCAGCAG T C EPB41L2 Ensembl:ENSG00000079819 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:130869923..130870024 32194978 MeRIP-seq:(Medium) rs767521418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7540124,Human_RBP_ID_8630917,Human_RBP_ID_22513235,Human_RBP_ID_26354372 RMVar_hsa_circ_12549,RMVar_hsa_circ_350401,RMVar_hsa_circ_358792,RMVar_hsa_circ_64254,RMVar_hsa_circ_13144,RMVar_hsa_circ_352290 72309 RMVar_ID_72309 Human_SNP_ID_296646726 m1A Human chr6 - 130956045 130956045 130956045 CAAGAGATTAAAGTTGAAGTCAAGGAAGAAAAACCCTCAGTGAGCAAGGAAGAAAAACCCTCAGT CAAGAGATTAAAGTTGAAGTCAAGGAAGAAAAGCCCTCAGTGAGCAAGGAAGAAAAACCCTCAGT T C EPB41L2 Ensembl:ENSG00000079819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:130955974..130956167 26863196 MeRIP-seq:(Medium) rs1459968206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_215504,Human_RBP_ID_950034,Human_RBP_ID_2008465,Human_RBP_ID_18854209,Human_RBP_ID_24548628,Human_RBP_ID_26354379 Human_Splice_Rec_810407,Human_Splice_Rec_810439,Human_Splice_Rec_810473,Human_Splice_Rec_810511,Human_Splice_Rec_810543,Human_Splice_Rec_810593,Human_Splice_Rec_810621,Human_Splice_Rec_810659,Human_Splice_Rec_810709,Human_Splice_Rec_810743,Human_Splice_Rec_810769,Human_Splice_Rec_810799,Human_Splice_Rec_810883,Human_Splice_Rec_810937 RMVar_hsa_circ_64254,RMVar_hsa_circ_62474,RMVar_hsa_circ_328987,RMVar_hsa_circ_58482,RMVar_hsa_circ_75440,RMVar_hsa_circ_241493,RMVar_hsa_circ_268381,RMVar_hsa_circ_69133,RMVar_hsa_circ_301543,RMVar_hsa_circ_241492,RMVar_hsa_circ_306710 72310 RMVar_ID_72310 Human_SNP_ID_296646852 m1A Human chr6 - 130956432 130956432 130956432 GTGTCTGAAGTGAAGAAGGACTCTAGCCAGTTAGGAACAGATGCAACCAAGGAAAAACCTAAAGA GTGTCTGAAGTGAAGAAGGACTCTAGCCAGTTGGGAACAGATGCAACCAAGGAAAAACCTAAAGA T C EPB41L2 Ensembl:ENSG00000079819 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:130955146..130970304 26863196 MeRIP-seq:(Medium) rs1005636896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2008467,Human_RBP_ID_5532733,Human_RBP_ID_5617314,Human_RBP_ID_7540333,Human_RBP_ID_8896392,Human_RBP_ID_9401121,Human_RBP_ID_10254984,Human_RBP_ID_15644344,Human_RBP_ID_24548821,Human_RBP_ID_26354382,Human_RBP_ID_27828015 Human_Splice_Rec_810406,Human_Splice_Rec_810438,Human_Splice_Rec_810472,Human_Splice_Rec_810510,Human_Splice_Rec_810542,Human_Splice_Rec_810592,Human_Splice_Rec_810620,Human_Splice_Rec_810658,Human_Splice_Rec_810708,Human_Splice_Rec_810798,Human_Splice_Rec_810936,Human_Splice_Rec_810940,Human_Splice_Rec_810944,Human_Splice_Rec_810946,Human_Splice_Rec_810948 RMVar_hsa_circ_64254,RMVar_hsa_circ_62474,RMVar_hsa_circ_328987,RMVar_hsa_circ_58482,RMVar_hsa_circ_75440,RMVar_hsa_circ_241493,RMVar_hsa_circ_268381,RMVar_hsa_circ_69133,RMVar_hsa_circ_301543,RMVar_hsa_circ_241492,RMVar_hsa_circ_306710 72311 RMVar_ID_72311 Human_SNP_ID_296646858 m1A Human chr6 - 130956448 130956446 130956449 TACTGAAGTAGGCTCTGTGTCTGAAGTGAAGAAGGACTCTAGCCAGTTAGGAACAGATGCAACCA TACTGAAGTAGGCTCTGTGTCTGAAGTGAAG___GACTCTAGCCAGTTAGGAACAGATGCAACCA CCTT C EPB41L2 Ensembl:ENSG00000079819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:130956218..130956525;chr6:130956239..130956528 26863196 MeRIP-seq:(Medium) rs778438093 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2008467,Human_RBP_ID_3793381,Human_RBP_ID_4864148,Human_RBP_ID_5532733,Human_RBP_ID_7540333,Human_RBP_ID_9401121,Human_RBP_ID_24548488,Human_RBP_ID_26354382,Human_RBP_ID_27828912 Human_Splice_Rec_810406,Human_Splice_Rec_810438,Human_Splice_Rec_810472,Human_Splice_Rec_810510,Human_Splice_Rec_810542,Human_Splice_Rec_810592,Human_Splice_Rec_810620,Human_Splice_Rec_810658,Human_Splice_Rec_810708,Human_Splice_Rec_810798,Human_Splice_Rec_810936,Human_Splice_Rec_810940,Human_Splice_Rec_810944,Human_Splice_Rec_810946,Human_Splice_Rec_810948 RMVar_hsa_circ_64254,RMVar_hsa_circ_62474,RMVar_hsa_circ_328987,RMVar_hsa_circ_58482,RMVar_hsa_circ_75440,RMVar_hsa_circ_241493,RMVar_hsa_circ_268381,RMVar_hsa_circ_69133,RMVar_hsa_circ_301543,RMVar_hsa_circ_241492,RMVar_hsa_circ_306710 72312 RMVar_ID_72312 Human_SNP_ID_296646859 m1A Human chr6 - 130956448 130956448 130956448 TACTGAAGTAGGCTCTGTGTCTGAAGTGAAGAAGGACTCTAGCCAGTTAGGAACAGATGCAACCA TACTGAAGTAGGCTCTGTGTCTGAAGTGAAGACGGACTCTAGCCAGTTAGGAACAGATGCAACCA T G EPB41L2 Ensembl:ENSG00000079819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:130956218..130956525;chr6:130956239..130956528 26863196 MeRIP-seq:(Medium) rs1330727531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2008467,Human_RBP_ID_3793381,Human_RBP_ID_4864148,Human_RBP_ID_5532733,Human_RBP_ID_7540333,Human_RBP_ID_9401121,Human_RBP_ID_24548488,Human_RBP_ID_26354382,Human_RBP_ID_27828912 Human_Splice_Rec_810406,Human_Splice_Rec_810438,Human_Splice_Rec_810472,Human_Splice_Rec_810510,Human_Splice_Rec_810542,Human_Splice_Rec_810592,Human_Splice_Rec_810620,Human_Splice_Rec_810658,Human_Splice_Rec_810708,Human_Splice_Rec_810798,Human_Splice_Rec_810936,Human_Splice_Rec_810940,Human_Splice_Rec_810944,Human_Splice_Rec_810946,Human_Splice_Rec_810948 RMVar_hsa_circ_64254,RMVar_hsa_circ_62474,RMVar_hsa_circ_328987,RMVar_hsa_circ_58482,RMVar_hsa_circ_75440,RMVar_hsa_circ_241493,RMVar_hsa_circ_268381,RMVar_hsa_circ_69133,RMVar_hsa_circ_301543,RMVar_hsa_circ_241492,RMVar_hsa_circ_306710 72313 RMVar_ID_72313 Human_SNP_ID_296859817 m1A Human chr6 + 131808079 131808079 131808079 CGGCTGCGCGGGGGGCGGGAGCCGCGGCGGCGAGGGCGGGCGCGCTCCCCGGGAGGGCCCGGCGG CGGCTGCGCGGGGGGCGGGAGCCGCGGCGGCGGGGGCGGGCGCGCTCCCCGGGAGGGCCCGGCGG A G ENPP1 Ensembl:ENSG00000197594 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:131808032..131808225;chr6:131808035..131808266;chr6:131808037..131808203 26863196 MeRIP-seq:(Medium) rs1192891806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252454,Human_RBP_ID_3821805,Human_RBP_ID_4864217,Human_RBP_ID_5533214,Human_RBP_ID_8730320,Human_RBP_ID_9354662 72314 RMVar_ID_72314 Human_SNP_ID_296859829 m1A Human chr6 + 131808114 131808114 131808114 GCGGGCGCGCTCCCCGGGAGGGCCCGGCGGGGAACGGCCGCGATCGGGGCCGCAGCCACGCTGCC GCGGGCGCGCTCCCCGGGAGGGCCCGGCGGGGGACGGCCGCGATCGGGGCCGCAGCCACGCTGCC A G ENPP1 Ensembl:ENSG00000197594 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:131808066..131808203 26863196 MeRIP-seq:(Medium) rs985103461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821805,Human_RBP_ID_4903511,Human_RBP_ID_5533214,Human_RBP_ID_8730320,Human_RBP_ID_9354662 72315 RMVar_ID_72315 Human_SNP_ID_296895197 m1A Human chr6 - 131949452 131949452 131949452 AGACATACCGAGCTAAATTCTGTGGAGTATGTACCGACGGCCGATGCTGCACCCCCCACAGAACC AGACATACCGAGCTAAATTCTGTGGAGTATGTGCCGACGGCCGATGCTGCACCCCCCACAGAACC T C CCN2 Ensembl:ENSG00000118523 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:131949401..131949500 32194978 MeRIP-seq:(Medium) rs759957908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790041,Human_RBP_ID_22773722 Human_miRNA_ID_1936851,Human_miRNA_ID_1947951 RMVar_hsa_circ_88541,RMVar_hsa_circ_110303,RMVar_hsa_circ_241546,RMVar_hsa_circ_241547 72316 RMVar_ID_72316 Human_SNP_ID_296895541 m1A Human chr6 - 131950418 131950418 131950418 ACGGGGCGGTGGGCTGCATGCCCCTGTGCAGCATGGACGTTCGTCTGCCCAGCCCTGACTGCCCC ACGGGGCGGTGGGCTGCATGCCCCTGTGCAGCGTGGACGTTCGTCTGCCCAGCCCTGACTGCCCC T C CCN2 Ensembl:ENSG00000118523 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:131950369..131950452 26863196 MeRIP-seq:(Medium) rs772459582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22461429,Human_RBP_ID_22513244,Human_RBP_ID_22773728 Human_miRNA_ID_2896380 RMVar_hsa_circ_110303,RMVar_hsa_circ_241547,RMVar_hsa_circ_18926 72317 RMVar_ID_72317 Human_SNP_ID_296895951 m1A Human chr6 + 131951267 131951267 131951267 AGCGCTGGCGGTGGTCGGAGGTGGGGACCGGGACGCGCCGGGCTGTCGTCTCGGGGCTGTCGGCC AGCGCTGGCGGTGGTCGGAGGTGGGGACCGGGTCGCGCCGGGCTGTCGTCTCGGGGCTGTCGGCC A T AL133346.1 Ensembl:ENSG00000227220 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:131951192..132077245 26863410 MeRIP-seq:(Medium) rs940069211 Functional Loss SNV dbSNP153 33..33 33 - - - 72318 RMVar_ID_72318 Human_SNP_ID_296986342 m1A Human chr6 + 132328443 132328441 132328443 CCACCTCTCCACCAATAGCCCAGGCAAAAATCACAGTTTCACAGGTGAGGAATGCATCGGGCATG CCACCTCTCCACCAATAGCCCAGGCAAAAAT__CAGTTTCACAGGTGAGGAATGCATCGGGCATG TCA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:132328097..132328547 32194978 MeRIP-seq:(Medium) rs749254614 Functional Loss DEL dbSNP153 32..33 33 - - - 72319 RMVar_ID_72319 Human_SNP_ID_297031339 m1A Human chr6 + 132513056 132513056 132513056 CCTCCTACACCTCCGACCGCCGTCACCCACCTACCCCGGAGCCCTCAGCTGCAATTCTCAGCTGA CCTCCTACACCTCCGACCGCCGTCACCCACCTGCCCCGGAGCCCTCAGCTGCAATTCTCAGCTGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr6:132512941..132513074;chr6:132512931..132513060 26863196 MeRIP-seq:(Medium) rs1017946490 Functional Loss SNV dbSNP153 33..33 33 - - - 72320 RMVar_ID_72320 Human_SNP_ID_297108335 m1A Human chr6 + 132798483 132798483 132798483 CTCCATCCCCGGTGCGTGGACTCCGGCGCCCCAGCTCCCGGCTTCAAGCCACGTCCTTGGACTCG CTCCATCCCCGGTGCGTGGACTCCGGCGCCCCGGCTCCCGGCTTCAAGCCACGTCCTTGGACTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:132798433..132798571 26863196 MeRIP-seq:(Medium) rs951867631 Functional Loss SNV dbSNP153 33..33 33 - - - 72321 RMVar_ID_72321 Human_SNP_ID_297108340 m1A Human chr6 + 132798497 132798497 132798497 CGTGGACTCCGGCGCCCCAGCTCCCGGCTTCAAGCCACGTCCTTGGACTCGACCTCCAAGGAGCC CGTGGACTCCGGCGCCCCAGCTCCCGGCTTCAGGCCACGTCCTTGGACTCGACCTCCAAGGAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:132798453..132798564 26863196 MeRIP-seq:(Medium) rs763689541 Functional Loss SNV dbSNP153 33..33 33 - - - 72322 RMVar_ID_72322 Human_SNP_ID_297112682 m1A Human chr6 - 132814610 132814610 132814610 ACACCCCCCTGCCGCCTCGCTCAACTTACCCCAAGCCTCCGCCTCCGCGCGACTCGGCGGCGGCA ACACCCCCCTGCCGCCTCGCTCAACTTACCCCGAGCCTCCGCCTCCGCGCGACTCGGCGGCGGCA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:132814596..132814696 26863410 MeRIP-seq:(Medium) rs897106328 Functional Loss SNV dbSNP153 33..33 33 - - - 72323 RMVar_ID_72323 Human_SNP_ID_297112683 m1A Human chr6 - 132814610 132814610 132814610 ACACCCCCCTGCCGCCTCGCTCAACTTACCCCAAGCCTCCGCCTCCGCGCGACTCGGCGGCGGCA ACACCCCCCTGCCGCCTCGCTCAACTTACCCCCAGCCTCCGCCTCCGCGCGACTCGGCGGCGGCA T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:132814596..132814696 26863410 MeRIP-seq:(Medium) rs897106328 Functional Loss SNV dbSNP153 33..33 33 - - - 72324 RMVar_ID_72324 Human_SNP_ID_297112779 m1A Human chr6 + 132814739 132814739 132814739 ACAAGTCAATGCTTTTGTTTTTTAGTGCGTTCAAGATTCAACTTCACCCGTAACCCACCGCCATG ACAAGTCAATGCTTTTGTTTTTTAGTGCGTTCGAGATTCAACTTCACCCGTAACCCACCGCCATG A G RPS12 Ensembl:ENSG00000112306 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:132814726..132815050 26863410 MeRIP-seq:(Medium) rs1459573710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_653349,Human_RBP_ID_1664090,Human_RBP_ID_2008682,Human_RBP_ID_2972389,Human_RBP_ID_4864503,Human_RBP_ID_5450463,Human_RBP_ID_5477354,Human_RBP_ID_8631127,Human_RBP_ID_9187955,Human_RBP_ID_17304679,Human_RBP_ID_17533631,Human_RBP_ID_18064197,Human_RBP_ID_22513256,Human_RBP_ID_22829519,Human_RBP_ID_24434851,Human_RBP_ID_24510136 Human_Splice_Rec_812584,Human_Splice_Rec_812585,Human_Splice_Rec_812594,Human_Splice_Rec_812595 RMVar_hsa_circ_80386,RMVar_hsa_circ_92431,RMVar_hsa_circ_109656,RMVar_hsa_circ_122890,RMVar_hsa_circ_102829,RMVar_hsa_circ_241576,RMVar_hsa_circ_241578,RMVar_hsa_circ_86524,RMVar_hsa_circ_241579,RMVar_hsa_circ_241577,RMVar_hsa_circ_314527,RMVar_hsa_circ_241575,RMVar_hsa_circ_297812,RMVar_hsa_circ_241580 72325 RMVar_ID_72325 Human_SNP_ID_297112793 m1A Human chr6 - 132814750 132814750 132814750 CCTTCCTCGGCCATGGCGGTGGGTTACGGGTGAAGTTGAATCTTGAACGCACTAAAAAACAAAAG CCTTCCTCGGCCATGGCGGTGGGTTACGGGTGTAGTTGAATCTTGAACGCACTAAAAAACAAAAG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:132814726..132814750 26863196 MeRIP-seq:(Medium) rs755357029 Functional Loss SNV dbSNP153 33..33 33 - - - 72326 RMVar_ID_72326 Human_SNP_ID_297112848 m1A Human chr6 - 132814820 132814820 132814820 TTCCGCCAGCTCTAGCCCCACGCCTCAGCCGCACCCCGACCCCAACTCCAACCCCGGCCCCTGGG TTCCGCCAGCTCTAGCCCCACGCCTCAGCCGCCCCCCGACCCCAACTCCAACCCCGGCCCCTGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:132814814..132814972 26863196 MeRIP-seq:(Medium) rs780383422 Functional Loss SNV dbSNP153 33..33 33 - - - 72327 RMVar_ID_72327 Human_SNP_ID_297112956 m1A Human chr6 + 132814995 132814995 132814995 GCGTTTAAGCATTGCTGCTGGAGGTGTAATGGACGTTAATACTGCTTTACAAGAGGTTCTGAAGA GCGTTTAAGCATTGCTGCTGGAGGTGTAATGGGCGTTAATACTGCTTTACAAGAGGTTCTGAAGA A G RPS12 Ensembl:ENSG00000112306 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:132814910..132814995 26863196 MeRIP-seq:(Medium) rs148631804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79672,Human_RBP_ID_653353,Human_RBP_ID_1664093,Human_RBP_ID_2008684,Human_RBP_ID_3793760,Human_RBP_ID_8631131,Human_RBP_ID_9187957,Human_RBP_ID_15647526,Human_RBP_ID_22829520,Human_RBP_ID_24135299,Human_RBP_ID_24434853,Human_RBP_ID_26532277,Human_RBP_ID_27088109,Human_RBP_ID_27340734 Human_Splice_Rec_812586,Human_Splice_Rec_812587,Human_Splice_Rec_812596 Human_miRNA_ID_3095715 RMVar_hsa_circ_80386,RMVar_hsa_circ_92431,RMVar_hsa_circ_109656,RMVar_hsa_circ_122890,RMVar_hsa_circ_102829,RMVar_hsa_circ_241576,RMVar_hsa_circ_241578,RMVar_hsa_circ_241577,RMVar_hsa_circ_314527,RMVar_hsa_circ_241575,RMVar_hsa_circ_297812,RMVar_hsa_circ_115467,RMVar_hsa_circ_241580,RMVar_hsa_circ_4639,RMVar_hsa_circ_241581 72328 RMVar_ID_72328 Human_SNP_ID_297112997 m1A Human chr6 + 132815059 132815059 132815059 ACTGCCCTCATCCACGATGGCCTAGCACGTGGAATTCGCGAAGCTGCCAAAGCCTTAGACAAGTA ACTGCCCTCATCCACGATGGCCTAGCACGTGGTATTCGCGAAGCTGCCAAAGCCTTAGACAAGTA A T RPS12 Ensembl:ENSG00000112306 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:132814726..132815150 32194978 MeRIP-seq:(Medium) rs1207181491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_653354,Human_RBP_ID_1664093,Human_RBP_ID_2008685,Human_RBP_ID_3793761,Human_RBP_ID_4864504,Human_RBP_ID_9187957,Human_RBP_ID_24135299,Human_RBP_ID_27088109,Human_RBP_ID_27340734 Human_Splice_Rec_812586,Human_Splice_Rec_812587,Human_Splice_Rec_812596 RMVar_hsa_circ_80386,RMVar_hsa_circ_92431,RMVar_hsa_circ_109656,RMVar_hsa_circ_122890,RMVar_hsa_circ_102829,RMVar_hsa_circ_241576,RMVar_hsa_circ_241578,RMVar_hsa_circ_241577,RMVar_hsa_circ_314527,RMVar_hsa_circ_241575,RMVar_hsa_circ_297812,RMVar_hsa_circ_115467,RMVar_hsa_circ_241580,RMVar_hsa_circ_4639,RMVar_hsa_circ_241581 72329 RMVar_ID_72329 Human_SNP_ID_297114044 m1A Human chr6 - 132816998 132816998 132816998 TTACGGGGTTTCCCCTCTCTGTCAATTTTACAAAGGCCTACCCATTCTCCTAGTTTCTTGTTGTC TTACGGGGTTTCCCCTCTCTGTCAATTTTACAGAGGCCTACCCATTCTCCTAGTTTCTTGTTGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:132816551..132817050 32194978 MeRIP-seq:(Medium) rs767661348 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 72330 RMVar_ID_72330 Human_SNP_ID_297218915 m1A Human chr6 + 133241421 133241421 133241421 CGCTGCCTTAGAGAGGGGGAAAGAGCTGCGGGAAAAGCCGGGGAGTGACGACTGCGGCGGCTGGG CGCTGCCTTAGAGAGGGGGAAAGAGCTGCGGGCAAAGCCGGGGAGTGACGACTGCGGCGGCTGGG A C EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:133241282..133241525 26863196 MeRIP-seq:(Medium) rs1022314958 Functional Loss SNV dbSNP153 33..33 33 - - - 72331 RMVar_ID_72331 Human_SNP_ID_297229482 m1A Human chr6 + 133285346 133285346 133285346 ACTCAAGAGAGGCGAGGAAGTGAGCCATGTGGATATCTGGGGAAAGTGGGTTTTAATTAGAGGGA ACTCAAGAGAGGCGAGGAAGTGAGCCATGTGGGTATCTGGGGAAAGTGGGTTTTAATTAGAGGGA A G EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:133285332..133285491 26863196 MeRIP-seq:(Medium) rs573863127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7542726 RMVar_hsa_circ_1637,RMVar_hsa_circ_241586,RMVar_hsa_circ_374745 72332 RMVar_ID_72332 Human_SNP_ID_297275729 m1A Human chr6 - 133480997 133480997 133480997 CCACCTCTCTCATCTTCCCTTCCACCTCTCCCATCTTCCCTTCCACCTCTCCCATCTTCCCTTCC CCACCTCTCTCATCTTCCCTTCCACCTCTCCCGTCTTCCCTTCCACCTCTCCCATCTTCCCTTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:133480987..133481110 26863196 MeRIP-seq:(Medium) rs970793138 Functional Loss SNV dbSNP153 33..33 33 - - - 72333 RMVar_ID_72333 Human_SNP_ID_297430362 m1A Human chr6 + 134133731 134133731 134133731 TCAATTTGGTGACCTCCTGGGAGCAAGGGACCACCAGCTTGCCTAAGGAGGGGTGAACCGGCCCA TCAATTTGGTGACCTCCTGGGAGCAAGGGACCGCCAGCTTGCCTAAGGAGGGGTGAACCGGCCCA A G RN7SL408P Ensembl:ENSG00000266875 Other exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:134133679..134133777 26863196 MeRIP-seq:(Medium) rs1253095194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5305712,Human_RBP_ID_8271714,Human_RBP_ID_21261045,Human_RBP_ID_22832544 Human_miRNA_ID_3128422 72334 RMVar_ID_72334 Human_SNP_ID_297439782 m1A Human chr6 - 134170426 134170426 134170426 GTGTTTTTCCCTTCCCGTCACAGAGTGGGCCCAACGACCTACGGCACTTTGACCCCGAGTTTACC GTGTTTTTCCCTTCCCGTCACAGAGTGGGCCCTACGACCTACGGCACTTTGACCCCGAGTTTACC T A SGK1 Ensembl:ENSG00000118515 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:134170401..134170425 26863196 MeRIP-seq:(Medium) rs1033588661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951074,Human_RBP_ID_5216951,Human_RBP_ID_22683186,Human_RBP_ID_22746309,Human_RBP_ID_24562414,Human_RBP_ID_25965556 Human_Splice_Rec_813268,Human_Splice_Rec_813292,Human_Splice_Rec_813302,Human_Splice_Rec_813324,Human_Splice_Rec_813344,Human_Splice_Rec_813364,Human_Splice_Rec_813386,Human_Splice_Rec_813406 Human_miRNA_ID_1941909,Human_miRNA_ID_1944952,Human_miRNA_ID_2116100,Human_miRNA_ID_2199673,Human_miRNA_ID_2202740,Human_miRNA_ID_2515730,Human_miRNA_ID_2815201,Human_miRNA_ID_2845317,Human_miRNA_ID_2848338,Human_miRNA_ID_2862464,Human_miRNA_ID_3112192 RMVar_hsa_circ_85452,RMVar_hsa_circ_241602 72335 RMVar_ID_72335 Human_SNP_ID_297441062 m1A Human chr6 - 134174514 134174514 134174514 TCAGAAGATTGCCAATAACTCCTATGCATGCAAACAGTAAGTTTGACCGGATTTGAGGAAATAAC TCAGAAGATTGCCAATAACTCCTATGCATGCAGACAGTAAGTTTGACCGGATTTGAGGAAATAAC T C SGK1 Ensembl:ENSG00000118515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:134174501..134174550 26863196 MeRIP-seq:(Medium) rs777715286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951087,Human_RBP_ID_3027433,Human_RBP_ID_5398375,Human_RBP_ID_5617335,Human_RBP_ID_19017457 Human_Splice_Rec_813248,Human_Splice_Rec_813249,Human_Splice_Rec_813270,Human_Splice_Rec_813272,Human_Splice_Rec_813273,Human_Splice_Rec_813304,Human_Splice_Rec_813305,Human_Splice_Rec_813326,Human_Splice_Rec_813327,Human_Splice_Rec_813345,Human_Splice_Rec_813366,Human_Splice_Rec_813367,Human_Splice_Rec_813388,Human_Splice_Rec_813389,Human_Splice_Rec_813442,Human_Splice_Rec_813443,Human_Splice_Rec_813458,Human_Splice_Rec_813459,Human_Splice_Rec_813470,Human_Splice_Rec_813471,Human_Splice_Rec_813480,Human_Splice_Rec_813481,Human_Splice_Rec_813488,Human_Splice_Rec_813489,Human_Splice_Rec_813500,Human_Splice_Rec_813501,Human_Splice_Rec_813506,Human_Splice_Rec_813507,Human_Splice_Rec_813510,Human_Splice_Rec_813511,Human_Splice_Rec_813513 RMVar_hsa_circ_33385,RMVar_hsa_circ_68106,RMVar_hsa_circ_44759,RMVar_hsa_circ_124758,RMVar_hsa_circ_241604 72336 RMVar_ID_72336 Human_SNP_ID_297441063 m1A Human chr6 - 134174514 134174514 134174514 TCAGAAGATTGCCAATAACTCCTATGCATGCAAACAGTAAGTTTGACCGGATTTGAGGAAATAAC TCAGAAGATTGCCAATAACTCCTATGCATGCACACAGTAAGTTTGACCGGATTTGAGGAAATAAC T G SGK1 Ensembl:ENSG00000118515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:134174501..134174550 26863196 MeRIP-seq:(Medium) rs777715286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951087,Human_RBP_ID_3027433,Human_RBP_ID_5398375,Human_RBP_ID_5617335,Human_RBP_ID_19017457 Human_Splice_Rec_813248,Human_Splice_Rec_813249,Human_Splice_Rec_813270,Human_Splice_Rec_813272,Human_Splice_Rec_813273,Human_Splice_Rec_813304,Human_Splice_Rec_813305,Human_Splice_Rec_813326,Human_Splice_Rec_813327,Human_Splice_Rec_813345,Human_Splice_Rec_813366,Human_Splice_Rec_813367,Human_Splice_Rec_813388,Human_Splice_Rec_813389,Human_Splice_Rec_813442,Human_Splice_Rec_813443,Human_Splice_Rec_813458,Human_Splice_Rec_813459,Human_Splice_Rec_813470,Human_Splice_Rec_813471,Human_Splice_Rec_813480,Human_Splice_Rec_813481,Human_Splice_Rec_813488,Human_Splice_Rec_813489,Human_Splice_Rec_813500,Human_Splice_Rec_813501,Human_Splice_Rec_813506,Human_Splice_Rec_813507,Human_Splice_Rec_813510,Human_Splice_Rec_813511,Human_Splice_Rec_813513 RMVar_hsa_circ_33385,RMVar_hsa_circ_68106,RMVar_hsa_circ_44759,RMVar_hsa_circ_124758,RMVar_hsa_circ_241604 72337 RMVar_ID_72337 Human_SNP_ID_297441690 m1A Human chr6 - 134175654 134175654 134175654 CCGCGCGCCCCGCCGCCCGCTGCCCATGGGGGAGATGCAGGGCGCGCTGGCCAGAGCCCGGCTCG CCGCGCGCCCCGCCGCCCGCTGCCCATGGGGGCGATGCAGGGCGCGCTGGCCAGAGCCCGGCTCG T G SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:134175605..134175700 26863196 MeRIP-seq:(Medium) rs777693371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33385 72338 RMVar_ID_72338 Human_SNP_ID_297442336 m1A Human chr6 + 134177774 134177773 134177774 GGCTGGAGGTAGAGCCCAGTTATGGCTGGAATAAGCCTCCCTGCTACATGCCTCTGATAAGCTGG GGCTGGAGGTAGAGCCCAGTTATGGCTGGAAT_AGCCTCCCTGCTACATGCCTCTGATAAGCTGG TA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:134177724..134177826 26863196 MeRIP-seq:(Medium) rs1376898504 Functional Loss DEL dbSNP153 33..33 33 - - - 72339 RMVar_ID_72339 Human_SNP_ID_590418093 m1A Human chr16 + 51595 51595 51595 GTAGAGTCAACATTCTCCCAGGCAGCTGCTCCACCAAGCACATCATCCACTTCTTTCAGTTTTGG GTAGAGTCAACATTCTCCCAGGCAGCTGCTCCCCCAAGCACATCATCCACTTCTTTCAGTTTTGG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:47549..51699 32194978 MeRIP-seq:(Medium) rs999184884 Functional Loss SNV dbSNP153 33..33 33 - - - 72340 RMVar_ID_72340 Human_SNP_ID_590418094 m1A Human chr16 + 51595 51595 51595 GTAGAGTCAACATTCTCCCAGGCAGCTGCTCCACCAAGCACATCATCCACTTCTTTCAGTTTTGG GTAGAGTCAACATTCTCCCAGGCAGCTGCTCCGCCAAGCACATCATCCACTTCTTTCAGTTTTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:47549..51699 32194978 MeRIP-seq:(Medium) rs999184884 Functional Loss SNV dbSNP153 33..33 33 - - - 72341 RMVar_ID_72341 Human_SNP_ID_590418118 m1A Human chr16 - 51643 51643 51643 ACTTGGAGTCTGAAGTGTTGTTTTTGTTAGGTAACAAATCGGAAGTACCCAAAACTGAAAGAAGT ACTTGGAGTCTGAAGTGTTGTTTTTGTTAGGTGACAAATCGGAAGTACCCAAAACTGAAAGAAGT T C POLR3K Ensembl:ENSG00000161980 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:51618..51694 26863196 MeRIP-seq:(Medium) rs779993458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512098,Human_RBP_ID_27811390 Human_Splice_Rec_1652236,Human_Splice_Rec_1652237,Human_Splice_Rec_1652239 72342 RMVar_ID_72342 Human_SNP_ID_590418780 m1A Human chr16 - 53307 53306 53308 GATCTGTGGGCTCTACTTTCCAATACACTCAGAAAGCCCCACCGTTTCCCACCGCCTTGGGTTCC GATCTGTGGGCTCTACTTTCCAATACACTCA__AAGCCCCACCGTTTCCCACCGCCTTGGGTTCC TTC T POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:53305..53405 26863196 MeRIP-seq:(Medium) rs1255627028 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17871325 72343 RMVar_ID_72343 Human_SNP_ID_590419121 m1A Human chr16 + 53913 53913 53913 CAGAGCCCGGCTGAGAGGGGCGGCCCTGGAGGAGACGGAGGCCGCGGGTGGGCCCGAGGCGCAAG CAGAGCCCGGCTGAGAGGGGCGGCCCTGGAGGTGACGGAGGCCGCGGGTGGGCCCGAGGCGCAAG A T SNRNP25 Ensembl:ENSG00000161981 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:53826..54093 26863196 MeRIP-seq:(Medium) rs1039606155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46272,Human_RBP_ID_234969,Human_RBP_ID_4393368,Human_RBP_ID_5113741,Human_RBP_ID_8941286,Human_RBP_ID_9371974,Human_RBP_ID_17067704,Human_RBP_ID_17652832,Human_RBP_ID_22442304,Human_RBP_ID_26328313,Human_RBP_ID_27811391 72344 RMVar_ID_72344 Human_SNP_ID_590419152 m1A Human chr16 + 53985 53985 53985 TGAGGACGAAGAAGAGGCGCTGCCGCACTCCGAGGCCATGGACGTGTTCCAGGAGGGTCTGGCTA TGAGGACGAAGAAGAGGCGCTGCCGCACTCCGCGGCCATGGACGTGTTCCAGGAGGGTCTGGCTA A C SNRNP25 Ensembl:ENSG00000161981 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:53886..54031 26863196 MeRIP-seq:(Medium) rs753476240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4349574,Human_RBP_ID_5113247,Human_RBP_ID_5465766,Human_RBP_ID_8941286,Human_RBP_ID_9324651,Human_RBP_ID_9371975,Human_RBP_ID_17653152,Human_RBP_ID_26328008,Human_RBP_ID_26769030,Human_RBP_ID_26937941,Human_RBP_ID_27811391 Human_Splice_Rec_1652241,Human_Splice_Rec_1652249,Human_Splice_Rec_1652257,Human_Splice_Rec_1652267,Human_Splice_Rec_1652271 72345 RMVar_ID_72345 Human_SNP_ID_590419159 m1A Human chr16 + 54003 54003 54003 GCTGCCGCACTCCGAGGCCATGGACGTGTTCCAGGAGGGTCTGGCTATGGTGGTGCAGGACCCGC GCTGCCGCACTCCGAGGCCATGGACGTGTTCCCGGAGGGTCTGGCTATGGTGGTGCAGGACCCGC A C SNRNP25 Ensembl:ENSG00000161981 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:53855..54088 26863196 MeRIP-seq:(Medium) rs1472244535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393369,Human_RBP_ID_5113247,Human_RBP_ID_5465766,Human_RBP_ID_8941286,Human_RBP_ID_9371976,Human_RBP_ID_17653152,Human_RBP_ID_26328008,Human_RBP_ID_26769030,Human_RBP_ID_27811392 Human_Splice_Rec_1652241,Human_Splice_Rec_1652249,Human_Splice_Rec_1652257,Human_Splice_Rec_1652267,Human_Splice_Rec_1652271 72346 RMVar_ID_72346 Human_SNP_ID_590419660 m1A Human chr16 - 55453 55453 55453 TTGGGAGTTGACTTCTTCCAGAGTAACCTACAAAAGACCAAGGGCAGAAGTGGGAACCCTGGCTC TTGGGAGTTGACTTCTTCCAGAGTAACCTACAGAAGACCAAGGGCAGAAGTGGGAACCCTGGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:55451..55550 26863196 MeRIP-seq:(Medium) rs781299134 Functional Loss SNV dbSNP153 33..33 33 - - - 72347 RMVar_ID_72347 Human_SNP_ID_590419777 m1A Human chr16 - 55780 55780 55780 GGTCCAGGACTGTGGCACTCTGCACTACAACCACGGCTGCAACCACGGACACAGATGGGAGAAGA GGTCCAGGACTGTGGCACTCTGCACTACAACCGCGGCTGCAACCACGGACACAGATGGGAGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:55776..55825 26863196 MeRIP-seq:(Medium) rs755463557 Functional Loss SNV dbSNP153 33..33 33 - - - 72348 RMVar_ID_72348 Human_SNP_ID_590420016 m1A Human chr16 + 56559 56559 56559 CCCCTCTTGCAGGTCCTACGTGTGGAGGACGTACCATCTGACCTCTGCAGGAGAGAAACTCACGG CCCCTCTTGCAGGTCCTACGTGTGGAGGACGTGCCATCTGACCTCTGCAGGAGAGAAACTCACGG A G SNRNP25 Ensembl:ENSG00000161981 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:56555..57126 32194978 MeRIP-seq:(Medium) rs779593421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1837861,Human_RBP_ID_4349699,Human_RBP_ID_9371980,Human_RBP_ID_17883617,Human_RBP_ID_22651237,Human_RBP_ID_23114005 Human_Splice_Rec_1652246,Human_Splice_Rec_1652247,Human_Splice_Rec_1652254,Human_Splice_Rec_1652255,Human_Splice_Rec_1652264,Human_Splice_Rec_1652265,Human_Splice_Rec_1652276,Human_Splice_Rec_1652280,Human_Splice_Rec_1652281,Human_Splice_Rec_1652285 72349 RMVar_ID_72349 Human_SNP_ID_590420253 m1A Human chr16 - 57275 57275 57275 TCCTGAGGGCCCCCAGGTTTATGCTGACAGTTACTGTTGGGCATGCCTGGGGTGAGGCCACCACA TCCTGAGGGCCCCCAGGTTTATGCTGACAGTTCCTGTTGGGCATGCCTGGGGTGAGGCCACCACA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57224..57373 32194978 MeRIP-seq:(Medium) rs1045001 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8850,GWAS_ID_8851,GWAS_ID_8852,GWAS_ID_8853,GWAS_ID_8854 72350 RMVar_ID_72350 Human_SNP_ID_590427232 m1A Human chr16 + 78322 78322 78322 GCCCCGGCCCGAGCCGCCGGATGCCCGCGCGCAGCGGGGCCCAGGTGAGCGCGCGCCTCGGCCGC GCCCCGGCCCGAGCCGCCGGATGCCCGCGCGCCGCGGGGCCCAGGTGAGCGCGCGCCTCGGCCGC A C MPG Ensembl:ENSG00000103152 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:78276..78388 26863196 MeRIP-seq:(Medium) rs1365673709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392669,Human_RBP_ID_19072530 Human_Splice_Rec_1652409,Human_Splice_Rec_1652415,Human_Splice_Rec_1652417 72351 RMVar_ID_72351 Human_SNP_ID_590427238 m1A Human chr16 - 78335 78335 78335 TCTGTTCCGCGGGGCGGCCGAGGCGCGCGCTCACCTGGGCCCCGCTGCGCGCGGGCATCCGGCGG TCTGTTCCGCGGGGCGGCCGAGGCGCGCGCTCGCCTGGGCCCCGCTGCGCGCGGGCATCCGGCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr16:78226..78378;chr16:78226..78380 26863196,26863410 MeRIP-seq:(Medium) rs1369950200 Functional Loss SNV dbSNP153 33..33 33 - - - 72352 RMVar_ID_72352 Human_SNP_ID_590429129 m1A Human chr16 + 83317 83317 83317 GAGGGCCGGCAGAGCCCTGTCCGCTAGCAGCCAGGGGACCACTAGGAGGACTGAGGTGGGGCCAG GAGGGCCGGCAGAGCCCTGTCCGCTAGCAGCCGGGGGACCACTAGGAGGACTGAGGTGGGGCCAG A G MPG Ensembl:ENSG00000103152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:83270..83496 26863196 MeRIP-seq:(Medium) rs1189258576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888161,Human_RBP_ID_18982721,Human_RBP_ID_19070245 72353 RMVar_ID_72353 Human_SNP_ID_590431192 m1A Human chr16 + 88773 88773 88773 CACTGAGGATGGCTGCGCGTTCATGCTCCGACAGGCTGGCCAGCAGGTTCTCCGTCATCCTCTGG CACTGAGGATGGCTGCGCGTTCATGCTCCGACGGGCTGGCCAGCAGGTTCTCCGTCATCCTCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88725..88912 26863196 MeRIP-seq:(Medium) rs1401753652 Functional Loss SNV dbSNP153 33..33 33 - - - 72354 RMVar_ID_72354 Human_SNP_ID_590431608 m1A Human chr16 - 89805 89803 89806 TGTCTGCCTGATGGCCTCACCCAGCGAGGAGGAGCCCCGTCCGCGAGAGGACGACGTCCCCTTCA TGTCTGCCTGATGGCCTCACCCAGCGAGGAG___CCCCGTCCGCGAGAGGACGACGTCCCCTTCA GCTC G NPRL3 Ensembl:ENSG00000103148 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89719..89919 32194978 MeRIP-seq:(Medium) rs765072700 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_233371,Human_RBP_ID_17371218,Human_RBP_ID_18189713 Human_Splice_Rec_1652450,Human_Splice_Rec_1652451,Human_Splice_Rec_1652472,Human_Splice_Rec_1652473,Human_Splice_Rec_1652498,Human_Splice_Rec_1652499,Human_Splice_Rec_1652520,Human_Splice_Rec_1652521,Human_Splice_Rec_1652540,Human_Splice_Rec_1652541 RMVar_hsa_circ_41368,RMVar_hsa_circ_298538,RMVar_hsa_circ_330473,RMVar_hsa_circ_45452,RMVar_hsa_circ_119834,RMVar_hsa_circ_26195,RMVar_hsa_circ_175278 72355 RMVar_ID_72355 Human_SNP_ID_590431609 m1A Human chr16 - 89805 89805 89805 TGTCTGCCTGATGGCCTCACCCAGCGAGGAGGAGCCCCGTCCGCGAGAGGACGACGTCCCCTTCA TGTCTGCCTGATGGCCTCACCCAGCGAGGAGGTGCCCCGTCCGCGAGAGGACGACGTCCCCTTCA T A NPRL3 Ensembl:ENSG00000103148 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89719..89919 32194978 MeRIP-seq:(Medium) rs1228580630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233371,Human_RBP_ID_17371218,Human_RBP_ID_18189713 Human_Splice_Rec_1652450,Human_Splice_Rec_1652451,Human_Splice_Rec_1652472,Human_Splice_Rec_1652473,Human_Splice_Rec_1652498,Human_Splice_Rec_1652499,Human_Splice_Rec_1652520,Human_Splice_Rec_1652521,Human_Splice_Rec_1652540,Human_Splice_Rec_1652541 RMVar_hsa_circ_41368,RMVar_hsa_circ_298538,RMVar_hsa_circ_330473,RMVar_hsa_circ_45452,RMVar_hsa_circ_119834,RMVar_hsa_circ_26195,RMVar_hsa_circ_175278 72356 RMVar_ID_72356 Human_SNP_ID_590434925 m1A Human chr16 - 100418 100418 100418 GCCTGCCCCACAAGATCCACTATGCGGCCTCCAGTCTGATCCCCCCAGAGGCCATCGAACGGAGC GCCTGCCCCACAAGATCCACTATGCGGCCTCCCGTCTGATCCCCCCAGAGGCCATCGAACGGAGC T G NPRL3 Ensembl:ENSG00000103148 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:100316..100476 26863196 MeRIP-seq:(Medium) rs1255211374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371221 Human_Splice_Rec_1652442,Human_Splice_Rec_1652443,Human_Splice_Rec_1652464,Human_Splice_Rec_1652465,Human_Splice_Rec_1652490,Human_Splice_Rec_1652491,Human_Splice_Rec_1652512,Human_Splice_Rec_1652513,Human_Splice_Rec_1652532,Human_Splice_Rec_1652533,Human_Splice_Rec_1652556,Human_Splice_Rec_1652557,Human_Splice_Rec_1652570,Human_Splice_Rec_1652571,Human_Splice_Rec_1652584,Human_Splice_Rec_1652585,Human_Splice_Rec_1652590,Human_Splice_Rec_1652591,Human_Splice_Rec_1652608,Human_Splice_Rec_1652609 Human_miRNA_ID_2424978,Human_miRNA_ID_2424979,Human_miRNA_ID_2434641,Human_miRNA_ID_2434642,Human_miRNA_ID_2568521,Human_miRNA_ID_2568522,Human_miRNA_ID_2653454,Human_miRNA_ID_2653455,Human_miRNA_ID_2754653,Human_miRNA_ID_2754654 RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_45452,RMVar_hsa_circ_119834,RMVar_hsa_circ_372855,RMVar_hsa_circ_175278,RMVar_hsa_circ_18523,RMVar_hsa_circ_175279,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_270125,RMVar_hsa_circ_15605,RMVar_hsa_circ_175282 72357 RMVar_ID_72357 Human_SNP_ID_590435386 m1A Human chr16 - 101583 101583 101583 CTGGATTTTGGACATCCCTGCAGGTGGAGCAGATGGGATTTGCTGATGGTTTAAAGTGGACTGTG CTGGATTTTGGACATCCCTGCAGGTGGAGCAGGTGGGATTTGCTGATGGTTTAAAGTGGACTGTG T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:101578..101931 26863196 MeRIP-seq:(Medium) rs1181658560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23679534 RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 72358 RMVar_ID_72358 Human_SNP_ID_590443721 m1A Human chr16 + 130569 130569 130569 TGCTCATCAGCATGGTCGCCCGTGTTGCTGGCAGCGTATCTGCTACGCGGCTTACCTGAGTCGGG TGCTCATCAGCATGGTCGCCCGTGTTGCTGGCCGCGTATCTGCTACGCGGCTTACCTGAGTCGGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:130556..138439 32194978 MeRIP-seq:(Medium) rs1382104978 Functional Loss SNV dbSNP153 33..33 33 - - - 72359 RMVar_ID_72359 Human_SNP_ID_590446264 m1A Human chr16 - 138216 138216 138216 CCATCAGCGTGATTCTGGTGAGCTCGGGGAGCAGGGGCAATAAGCTGCTGTTCAGGTACCCCTTC CCATCAGCGTGATTCTGGTGAGCTCGGGGAGCCGGGGCAATAAGCTGCTGTTCAGGTACCCCTTC T G NPRL3 Ensembl:ENSG00000103148 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:138176..138378 26863196 MeRIP-seq:(Medium) rs1218964632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4396549,Human_RBP_ID_5127945,Human_RBP_ID_5317115,Human_RBP_ID_6497036,Human_RBP_ID_12679963,Human_RBP_ID_17077790,Human_RBP_ID_17371223 Human_Splice_Rec_1652431,Human_Splice_Rec_1652455,Human_Splice_Rec_1652479,Human_Splice_Rec_1652503,Human_Splice_Rec_1652525,Human_Splice_Rec_1652561,Human_Splice_Rec_1652613,Human_Splice_Rec_1652623 Clinvar_Rec_305 72360 RMVar_ID_72360 Human_SNP_ID_590446275 m1A Human chr16 - 138255 138255 138255 GGCCCCGGCCCCACGGCGGGATGCGGGACAACACCAGCCCCATCAGCGTGATTCTGGTGAGCTCG GGCCCCGGCCCCACGGCGGGATGCGGGACAACGCCAGCCCCATCAGCGTGATTCTGGTGAGCTCG T C NPRL3 Ensembl:ENSG00000103148 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:138206..138418 26863196 MeRIP-seq:(Medium) rs1172482171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394136,Human_RBP_ID_5127946,Human_RBP_ID_5317115,Human_RBP_ID_17077282,Human_RBP_ID_18939817 Human_Splice_Rec_1652430,Human_Splice_Rec_1652478,Human_Splice_Rec_1652573,Human_Splice_Rec_1652587,Human_Splice_Rec_1652612 72361 RMVar_ID_72361 Human_SNP_ID_590446342 m1A Human chr16 + 138348 138343 138348 AGCCGGAGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAG AGCCGGAGGCGGAGGGGGCCTGAGGAGG_____GCCGGAGGCGGAGGGGGCCTGAGGAGGACGAG GACGGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:138251..138603 26863196 MeRIP-seq:(Medium) rs1366027287 Functional Loss DEL dbSNP153 29..33 33 - - - 72362 RMVar_ID_72362 Human_SNP_ID_590446352 m1A Human chr16 + 138348 138348 138348 AGCCGGAGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAG AGCCGGAGGCGGAGGGGGCCTGAGGAGGACGGGGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:138251..138603 26863196 MeRIP-seq:(Medium) rs1415689766 Functional Loss SNV dbSNP153 33..33 33 - - - 72363 RMVar_ID_72363 Human_SNP_ID_590446359 m1A Human chr16 + 138354 138354 138354 AGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAGGCGGGG AGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGGGGCGGAGGGGGCCTGAGGAGGACGAGGCGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:138151..138415 26863196 MeRIP-seq:(Medium) rs1229931842 Functional Loss SNV dbSNP153 33..33 33 - - - 72364 RMVar_ID_72364 Human_SNP_ID_590446365 m1A Human chr16 + 138360 138360 138360 AGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAGGCGGGGACGCAG AGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGGGGGGGCCTGAGGAGGACGAGGCGGGGACGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:138315..138402 26863196 MeRIP-seq:(Medium) rs1333162899 Functional Loss SNV dbSNP153 33..33 33 - - - 72365 RMVar_ID_72365 Human_SNP_ID_590446399 m1A Human chr16 - 138414 138414 138414 ACCCCTGCCCTCCTCAGGCCCCCTCCGCCTCCACCCCTGCCCTCCTCAGGCCCCCTGCGTCCCCG ACCCCTGCCCTCCTCAGGCCCCCTCCGCCTCCCCCCCTGCCCTCCTCAGGCCCCCTGCGTCCCCG T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,H2O2 treatment;HEK293T,Starvation treatment chr16:138312..138612;chr16:138312..138463 26863410 MeRIP-seq:(Medium) rs1420287022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128355,Human_RBP_ID_17077282,Human_RBP_ID_17371225,Human_RBP_ID_17563667,Human_RBP_ID_18939817,Human_RBP_ID_25194789 72366 RMVar_ID_72366 Human_SNP_ID_590446400 m1A Human chr16 + 138417 138417 138417 GGACGCAGGGGGCCTGAGGAGGGCAGGGGTGGAGGCGGAGGGGGCCTGAGGAGGGCAGGGGTGGA GGACGCAGGGGGCCTGAGGAGGGCAGGGGTGGGGGCGGAGGGGGCCTGAGGAGGGCAGGGGTGGA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:138318..138498 26863410 MeRIP-seq:(Medium) rs1428482109 Functional Loss SNV dbSNP153 33..33 33 - - - 72367 RMVar_ID_72367 Human_SNP_ID_590458909 m1A Human chr16 + 175499 175497 175500 ACCCTGCAGGAGCTGGCCAGCCTCATCACCCCAACATCTCCCCACCTCCATTCTCCAACCACAGG ACCCTGCAGGAGCTGGCCAGCCTCATCACCC___CATCTCCCCACCTCCATTCTCCAACCACAGG CCAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:175449..175563 26863196 MeRIP-seq:(Medium) rs1356652641 Functional Loss DEL dbSNP153 32..34 33 - - - 72368 RMVar_ID_72368 Human_SNP_ID_590460882 m1A Human chr16 - 180575 180575 180575 GGGCGGGGGCGCCCAGCCTGCCGCACCTTTCCAGGGCCTCTGTCGTGTAGACGCCGACGTTGCTG GGGCGGGGGCGCCCAGCCTGCCGCACCTTTCCGGGGCCTCTGTCGTGTAGACGCCGACGTTGCTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:180501..180732 26863410 MeRIP-seq:(Medium) rs1307413670 Functional Loss SNV dbSNP153 33..33 33 - - - 72369 RMVar_ID_72369 Human_SNP_ID_590463149 m1A Human chr16 + 186050 186033 186050 GGAATACGGACACGGGAGGAATACGGACACGGAGGGAACAGCGACACGGGGGGAACAGCGACACG GGAATACGGACACGGG_________________GGGAACAGCGACACGGGGGGAACAGCGACACG GAGGAATACGGACACGGA G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:185953..186166;chr16:185995..186095;chr16:185995..186100;chr16:185992..186111;chr16:185946..186160 26863196 MeRIP-seq:(Medium) rs1416401478 Functional Loss DEL dbSNP153 17..33 33 - - - 72370 RMVar_ID_72370 Human_SNP_ID_590463151 m1A Human chr16 + 186050 186034 186051 GGAATACGGACACGGGAGGAATACGGACACGGAGGGAACAGCGACACGGGGGGAACAGCGACACG GGAATACGGACACGGGA_________________GGAACAGCGACACGGGGGGAACAGCGACACG AGGAATACGGACACGGAG A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:185953..186166;chr16:185995..186095;chr16:185995..186100;chr16:185992..186111;chr16:185946..186160 26863196 MeRIP-seq:(Medium) rs142394983 Functional Loss DEL dbSNP153 18..34 33 - - - 72371 RMVar_ID_72371 Human_SNP_ID_590463180 m1A Human chr16 + 186050 186049 186050 GGAATACGGACACGGGAGGAATACGGACACGGAGGGAACAGCGACACGGGGGGAACAGCGACACG GGAATACGGACACGGGAGGAATACGGACACGG_GGGAACAGCGACACGGGGGGAACAGCGACACG GA G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:185953..186166;chr16:185995..186095;chr16:185995..186100;chr16:185992..186111;chr16:185946..186160 26863196 MeRIP-seq:(Medium) rs879566530 Functional Loss DEL dbSNP153 33..33 33 - - - 72372 RMVar_ID_72372 Human_SNP_ID_590463181 m1A Human chr16 + 186050 186050 186050 GGAATACGGACACGGGAGGAATACGGACACGGAGGGAACAGCGACACGGGGGGAACAGCGACACG GGAATACGGACACGGGAGGAATACGGACACGGGGGGAACAGCGACACGGGGGGAACAGCGACACG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:185953..186166;chr16:185995..186095;chr16:185995..186100;chr16:185992..186111;chr16:185946..186160 26863196 MeRIP-seq:(Medium) rs2974775 Functional Loss SNV dbSNP153 33..33 33 - - - 72373 RMVar_ID_72373 Human_SNP_ID_590463190 m1A Human chr16 + 186054 186054 186054 TACGGACACGGGAGGAATACGGACACGGAGGGAACAGCGACACGGGGGGAACAGCGACACGGGGG TACGGACACGGGAGGAATACGGACACGGAGGGGACAGCGACACGGGGGGAACAGCGACACGGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:185995..186100 26863196 MeRIP-seq:(Medium) rs1477300208 Functional Loss SNV dbSNP153 33..33 33 - - - 72374 RMVar_ID_72374 Human_SNP_ID_590464360 m1A Human chr16 - 189251 189251 189251 GAGGGCCCCCGGACTGGAGGCTTGAGAGCTCCAACGGGAAGATGGCTTCACGGAGGTCAGAAGAG GAGGGCCCCCGGACTGGAGGCTTGAGAGCTCCGACGGGAAGATGGCTTCACGGAGGTCAGAAGAG T C LUC7L Ensembl:ENSG00000007392 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:189200..189351;chr16:189201..189365;chr16:189201..189370 26863196 MeRIP-seq:(Medium) rs781129574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471060,Human_RBP_ID_1514877,Human_RBP_ID_1839949,Human_RBP_ID_18161830 Human_Splice_Rec_1652702,Human_Splice_Rec_1652720,Human_Splice_Rec_1652754,Human_Splice_Rec_1652774,Human_Splice_Rec_1652778,Human_Splice_Rec_1652786,Human_Splice_Rec_1652806,Human_Splice_Rec_1652820,Human_Splice_Rec_1652824 RMVar_hsa_circ_175292 72375 RMVar_ID_72375 Human_SNP_ID_590465254 m1A Human chr16 - 192030 192030 192030 GAGGAGGTGGGAAGTAGAAGATGCCTCTGGCCACACTCAGCTTGAGAGGCCATCTTGAGGTGGGG GAGGAGGTGGGAAGTAGAAGATGCCTCTGGCCGCACTCAGCTTGAGAGGCCATCTTGAGGTGGGG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:192029..192361 26863196 MeRIP-seq:(Medium) rs905957705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471069,Human_RBP_ID_9419025,Human_RBP_ID_12697354,Human_RBP_ID_18938503,Human_RBP_ID_22583422 RMVar_hsa_circ_27658,RMVar_hsa_circ_175292,RMVar_hsa_circ_63159,RMVar_hsa_circ_378398 72376 RMVar_ID_72376 Human_SNP_ID_590467604 m1A Human chr16 + 199205 199205 199205 GACCTCGCAGACACGCAGCTTTTGCTGCTGAAAACTGGATGCAGGCATGGAATTTCTGTATTCTT GACCTCGCAGACACGCAGCTTTTGCTGCTGAAGACTGGATGCAGGCATGGAATTTCTGTATTCTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:199153..199240 26863410 MeRIP-seq:(Medium) rs112643318 Functional Loss SNV dbSNP153 33..33 33 - - - 72377 RMVar_ID_72377 Human_SNP_ID_590476885 m1A Human chr16 - 228329 228329 228329 GTTGCAGAAAGCCTCATGTTCATCGAGCCGTGAGTCACAACCAATTTCTAAGCTGTTATAACAAA GTTGCAGAAAGCCTCATGTTCATCGAGCCGTGCGTCACAACCAATTTCTAAGCTGTTATAACAAA T G LUC7L Ensembl:ENSG00000007392 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:228326..228454 26863410 MeRIP-seq:(Medium) rs1321611459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1281558,Human_RBP_ID_1840589,Human_RBP_ID_2472068,Human_RBP_ID_12707898 Human_Splice_Rec_1652756,Human_Splice_Rec_1652788,Human_Splice_Rec_1652840,Human_Splice_Rec_1652868,Human_Splice_Rec_1652914,Human_Splice_Rec_1652920,Human_Splice_Rec_1652922 Human_miRNA_ID_250810,Human_miRNA_ID_820507,Human_miRNA_ID_861109,Human_miRNA_ID_3067362 RMVar_hsa_circ_79555,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_175304,RMVar_hsa_circ_345851,RMVar_hsa_circ_72023 72378 RMVar_ID_72378 Human_SNP_ID_590477034 m1A Human chr16 - 228819 228819 228819 AAACCTGGCCCGCTCTGGTTCTGTACCATTGCAAGGGGAACCGTAAACTGAGCTTTTCTAACGTG AAACCTGGCCCGCTCTGGTTCTGTACCATTGCGAGGGGAACCGTAAACTGAGCTTTTCTAACGTG T C LUC7L Ensembl:ENSG00000007392 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:228815..229264 32194978 MeRIP-seq:(Medium) rs1231035465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515374,Human_RBP_ID_9068791,Human_RBP_ID_12707955 Human_Splice_Rec_1652921 Human_miRNA_ID_894895,Human_miRNA_ID_901559,Human_miRNA_ID_908206,Human_miRNA_ID_914850,Human_miRNA_ID_1279952 72379 RMVar_ID_72379 Human_SNP_ID_590477373 m1A Human chr16 + 229375 229375 229375 AGCCGGCGGAGGCGACGGGGTCGGCCGCGACGACTTCTCTCAGGCAGGCGGTGGCAGCGGCGTCG AGCCGGCGGAGGCGACGGGGTCGGCCGCGACGGCTTCTCTCAGGCAGGCGGTGGCAGCGGCGTCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:229266..229450 26863196 MeRIP-seq:(Medium) rs1056737283 Functional Loss SNV dbSNP153 33..33 33 - - - 72380 RMVar_ID_72380 Human_SNP_ID_590479280 m1A Human chr16 + 234856 234856 234856 AGCGGCGCGGTCGGGTGAGAGGCCGCGGCGGCAGGTGAGTGAGCGCGGCCTCGTACTCGCGCGTG AGCGGCGCGGTCGGGTGAGAGGCCGCGGCGGCCGGTGAGTGAGCGCGGCCTCGTACTCGCGCGTG A C FAM234A Ensembl:ENSG00000167930 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:234826..234932;chr16:234846..234950;chr16:234846..234935 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1224796442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392672 Human_Splice_Rec_1652923,Human_Splice_Rec_1652949,Human_Splice_Rec_1652977,Human_Splice_Rec_1653003,Human_Splice_Rec_1653031,Human_Splice_Rec_1653059,Human_Splice_Rec_1653067,Human_Splice_Rec_1653091,Human_Splice_Rec_1653095,Human_Splice_Rec_1653103,Human_Splice_Rec_1653107,Human_Splice_Rec_1653119,Human_Splice_Rec_1653131,Human_Splice_Rec_1653143,Human_Splice_Rec_1653167 72381 RMVar_ID_72381 Human_SNP_ID_590479317 m1A Human chr16 + 234908 234908 234908 GTACTCGCGCGTGCACGCCGCAGGGGCGCCGCAGGCCGCCCCTTCGCTCTGGGACCCCGGCCCCC GTACTCGCGCGTGCACGCCGCAGGGGCGCCGCTGGCCGCCCCTTCGCTCTGGGACCCCGGCCCCC A T FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:234897..235039 26863196 MeRIP-seq:(Medium) rs1319142287 Functional Loss SNV dbSNP153 33..33 33 - - - 72382 RMVar_ID_72382 Human_SNP_ID_590484237 m1A Human chr16 + 249529 249529 249529 ACCTTCGCAGGCTGCCTGAGCTGCACTTGACAAGTGGCTTTATGATCCCTAGGTCCACCTGGGCT ACCTTCGCAGGCTGCCTGAGCTGCACTTGACACGTGGCTTTATGATCCCTAGGTCCACCTGGGCT A C FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:249526..249600;chr16:249526..249675 26863196 MeRIP-seq:(Medium) rs1478321045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22540969,Human_RBP_ID_22654790,Human_RBP_ID_25204870 72383 RMVar_ID_72383 Human_SNP_ID_590489370 m1A Human chr16 - 264089 264089 264089 AGCGGTGGTCTGCGGTCGGCAGGCTGGCGGACAGTGGACCCCCAGGGAGGCTCGGGAGGGCTAGG AGCGGTGGTCTGCGGTCGGCAGGCTGGCGGACTGTGGACCCCCAGGGAGGCTCGGGAGGGCTAGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:264038..264186 26863196 MeRIP-seq:(Medium) rs767537349 Functional Loss SNV dbSNP153 33..33 33 - - - 72384 RMVar_ID_72384 Human_SNP_ID_590489777 m1A Human chr16 - 264968 264968 264968 AGCCGGGAGAACCGGTCCCTGATGGCTTGGTCACTGTCTGGCCCACCCTCACCCAGGCGGACCAC AGCCGGGAGAACCGGTCCCTGATGGCTTGGTCGCTGTCTGGCCCACCCTCACCCAGGCGGACCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:264917..265028 26863196 MeRIP-seq:(Medium) rs1348776379 Functional Loss SNV dbSNP153 33..33 33 - - - 72385 RMVar_ID_72385 Human_SNP_ID_590489932 m1A Human chr16 + 265363 265363 265363 GGCAGAGCTGGGTCATGCAGCACCCCATCCTTACCCGGTGCCCTCTCCTTGCCAGCTTCTCCCCA GGCAGAGCTGGGTCATGCAGCACCCCATCCTTTCCCGGTGCCCTCTCCTTGCCAGCTTCTCCCCA A T FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:265317..265393 26863196 MeRIP-seq:(Medium) rs1176849742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113755,Human_RBP_ID_18938504,Human_RBP_ID_26444615 Human_miRNA_ID_2621548 RMVar_hsa_circ_101634,RMVar_hsa_circ_123278,RMVar_hsa_circ_175308,RMVar_hsa_circ_175309 72386 RMVar_ID_72386 Human_SNP_ID_590490090 m1A Human chr16 + 265874 265874 265874 CCCTGAAGAGGCCCCGTGCCCCAGGCATGGCAAGCGCCTGCCTCTCCCCTTCCGGTGCTCACACG CCCTGAAGAGGCCCCGTGCCCCAGGCATGGCACGCGCCTGCCTCTCCCCTTCCGGTGCTCACACG A C FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:265824..266024 26863196 MeRIP-seq:(Medium) rs1189933356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17653165,Human_RBP_ID_22370084,Human_RBP_ID_26444618 Human_miRNA_ID_1261655,Human_miRNA_ID_2385111 RMVar_hsa_circ_101634,RMVar_hsa_circ_123278,RMVar_hsa_circ_175308,RMVar_hsa_circ_175309 72387 RMVar_ID_72387 Human_SNP_ID_590495952 m1A Human chr16 - 280430 280430 280430 GTCGCCCCCGCCGGCGTGCCAGGACCCCGCACAGAAGCGCCCGGACGCGGACGCACGCAGCCGCG GTCGCCCCCGCCGGCGTGCCAGGACCCCGCACTGAAGCGCCCGGACGCGGACGCACGCAGCCGCG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:280360..280472 26863410 MeRIP-seq:(Medium) rs1345118697 Functional Loss SNV dbSNP153 33..33 33 - - - 72388 RMVar_ID_72388 Human_SNP_ID_590496973 m1A Human chr16 + 282473 282427 282473 GGAACCCCTAATGCCTCTGTTCCCAGGTCCACAGGGAGATTGTCAGCGGCCTCAAGTGTCTGCAC _________________________________GGGAGATTGTCAGCGGCCTCAAGTGTCTGCAC GCCTGGCCCCCAGAGGAACCCCTAATGCCTCTGTTCCCAGGTCCACA G ARHGDIG Ensembl:ENSG00000242173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:281455..282960 32194978 MeRIP-seq:(Medium) rs1424535380 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_3948278 Human_Splice_Rec_1653412,Human_Splice_Rec_1653413,Human_Splice_Rec_1653422,Human_Splice_Rec_1653423,Human_Splice_Rec_1653432,Human_Splice_Rec_1653433,Human_Splice_Rec_1653440,Human_Splice_Rec_1653441 72389 RMVar_ID_72389 Human_SNP_ID_590500660 m1A Human chr16 - 288156 288154 288157 AGAGGACGAGGCCGTCCTGCCCGTCTTTGAGGAGAAGATCATCGGCAAAGTGGAGAAGGTGGACT AGAGGACGAGGCCGTCCTGCCCGTCTTTGAG___AAGATCATCGGCAAAGTGGAGAAGGTGGACT TCTC T AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:288001..288251 26863196 MeRIP-seq:(Medium) rs759595958 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_44205,Human_RBP_ID_473674,Human_RBP_ID_1066172,Human_RBP_ID_3946856,Human_RBP_ID_5114054 Human_Splice_Rec_1653546,Human_Splice_Rec_1653566,Human_Splice_Rec_1653584 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314 72390 RMVar_ID_72390 Human_SNP_ID_590501233 m1A Human chr16 + 289399 289399 289399 AAACCCTCTTTTTCATACCGTTGGGCACCCACATACTCGTGCGGGGAGGGGGCACCCCAGCCCTC AAACCCTCTTTTTCATACCGTTGGGCACCCACGTACTCGTGCGGGGAGGGGGCACCCCAGCCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:289397..289473 26863196 MeRIP-seq:(Medium) rs373737605 Functional Loss SNV dbSNP153 33..33 33 - - - 72391 RMVar_ID_72391 Human_SNP_ID_590501311 m1A Human chr16 + 289551 289551 289551 GGATGGGTTCCCCGCAGAAGTAGTACGCCACAACGATGCTGTCACACGGCTGGGCACTCCCGCCG GGATGGGTTCCCCGCAGAAGTAGTACGCCACAGCGATGCTGTCACACGGCTGGGCACTCCCGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:289501..289657 26863196 MeRIP-seq:(Medium) rs1220971406 Functional Loss SNV dbSNP153 33..33 33 - - - 72392 RMVar_ID_72392 Human_SNP_ID_590501347 m1A Human chr16 - 289606 289606 289606 CCAGGTACCACCGCTGCATCTCTTTCCCCAGGACAAGATCGCAGAGGAAGGTGGGCGGCGGGAGT CCAGGTACCACCGCTGCATCTCTTTCCCCAGGGCAAGATCGCAGAGGAAGGTGGGCGGCGGGAGT T C AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:289404..289625 26863196 MeRIP-seq:(Medium) rs777310323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888171,Human_RBP_ID_22540970,Human_RBP_ID_22651261 Human_Splice_Rec_1653564,Human_Splice_Rec_1653582,Human_Splice_Rec_1653586 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_293011,RMVar_hsa_circ_175317 72393 RMVar_ID_72393 Human_SNP_ID_590502919 m1A Human chr16 - 293562 293562 293562 ACCATGCCACCCCACCCAGCTCCCAACCCCCTAACCCAGCTGGAGGAGGCGCGCCGACGTCTGGA ACCATGCCACCCCACCCAGCTCCCAACCCCCTGACCCAGCTGGAGGAGGCGCGCCGACGTCTGGA T C AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:293513..293614 32194978 MeRIP-seq:(Medium) rs771010096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3946857 Human_Splice_Rec_1653561,Human_Splice_Rec_1653581,Human_Splice_Rec_1653585 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_293011,RMVar_hsa_circ_175317,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783 72394 RMVar_ID_72394 Human_SNP_ID_590502920 m1A Human chr16 - 293562 293562 293562 ACCATGCCACCCCACCCAGCTCCCAACCCCCTAACCCAGCTGGAGGAGGCGCGCCGACGTCTGGA ACCATGCCACCCCACCCAGCTCCCAACCCCCTCACCCAGCTGGAGGAGGCGCGCCGACGTCTGGA T G AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:293513..293614 32194978 MeRIP-seq:(Medium) rs771010096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3946857 Human_Splice_Rec_1653561,Human_Splice_Rec_1653581,Human_Splice_Rec_1653585 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_293011,RMVar_hsa_circ_175317,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783 72395 RMVar_ID_72395 Human_SNP_ID_590504182 m1A Human chr16 - 297059 297059 297059 AAAGGAGATCAGCAGGCACCGCAGGACCGGCCACGGGTGAGCACCCCGCACGCAGCCAGCCTCGT AAAGGAGATCAGCAGGCACCGCAGGACCGGCCTCGGGTGAGCACCCCGCACGCAGCCAGCCTCGT T A AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:297051..297075 26863196 MeRIP-seq:(Medium) rs771479456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889181,Human_RBP_ID_3948285,Human_RBP_ID_5114055,Human_RBP_ID_18984675,Human_RBP_ID_22653468,Human_RBP_ID_26328334,Human_RBP_ID_27810721 Human_Splice_Rec_1653543,Human_Splice_Rec_1653559,Human_Splice_Rec_1653579 RMVar_hsa_circ_84104,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314,RMVar_hsa_circ_117231,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783,RMVar_hsa_circ_286556,RMVar_hsa_circ_175319,RMVar_hsa_circ_175320 72396 RMVar_ID_72396 Human_SNP_ID_590504267 m1A Human chr16 - 297228 297228 297228 AGGCCAGGGCGACTCGCAGCTCTTGCCCTTGCAGTGGGAAGGTGGGCGTGGCGTGCAAAAGAAAT AGGCCAGGGCGACTCGCAGCTCTTGCCCTTGCTGTGGGAAGGTGGGCGTGGCGTGCAAAAGAAAT T A AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:297201..297250 26863196 MeRIP-seq:(Medium) rs1364610136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22542048 RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_117231,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783,RMVar_hsa_circ_286556,RMVar_hsa_circ_175319,RMVar_hsa_circ_175320 72397 RMVar_ID_72397 Human_SNP_ID_590504605 m1A Human chr16 - 297962 297962 297962 GGCACTGGGGGGTGCCGCCTCGGGGCACGGGAAGCACGTACCCAAGTCAGGGGCGAAGCTGGACG GGCACTGGGGGGTGCCGCCTCGGGGCACGGGAGGCACGTACCCAAGTCAGGGGCGAAGCTGGACG T C AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:297911..297994 26863196 MeRIP-seq:(Medium) rs1488818919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4367950,Human_RBP_ID_8811637,Human_RBP_ID_9285517,Human_RBP_ID_22497899,Human_RBP_ID_26769034 RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_117231,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783,RMVar_hsa_circ_286556,RMVar_hsa_circ_175319,RMVar_hsa_circ_175320,RMVar_hsa_circ_175321,RMVar_hsa_circ_126582 72398 RMVar_ID_72398 Human_SNP_ID_590504757 m1A Human chr16 - 298253 298252 298254 CTGAGAGGTGATGGTGCTGCTTGTCCCCACACAGGAGGAGGAAGGTGAGGACGGCGATCCATCGT CTGAGAGGTGATGGTGCTGCTTGTCCCCACA__GGAGGAGGAAGGTGAGGACGGCGATCCATCGT CTG C AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:298251..298275 26863196 MeRIP-seq:(Medium) rs1394686392 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_888174,Human_RBP_ID_5523825,Human_RBP_ID_22651262 RMVar_hsa_circ_85828,RMVar_hsa_circ_175316,RMVar_hsa_circ_117231,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_265783,RMVar_hsa_circ_175319 72399 RMVar_ID_72399 Human_SNP_ID_590511570 m1A Human chr16 + 319874 319874 319874 TGGTCCGGTTACATTTAGTGTGATGTGGAGGGAGCTGGGCCACCGTCGGATCGGGTTGGTTTATC TGGTCCGGTTACATTTAGTGTGATGTGGAGGGGGCTGGGCCACCGTCGGATCGGGTTGGTTTATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:319872..319991 26863196 MeRIP-seq:(Medium) rs1317774466 Functional Loss SNV dbSNP153 33..33 33 - - - 72400 RMVar_ID_72400 Human_SNP_ID_590517030 m1A Human chr16 + 335341 335341 335341 CAGGCACACCTCGGCCACTAGTCTGTACCAGGACACACTAATAACACAGCACACAGTACCACAGC CAGGCACACCTCGGCCACTAGTCTGTACCAGGGCACACTAATAACACAGCACACAGTACCACAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:335335..335474 32194978 MeRIP-seq:(Medium) rs911519987 Functional Loss SNV dbSNP153 33..33 33 - - - 72401 RMVar_ID_72401 Human_SNP_ID_590521056 m1A Human chr16 + 347083 347083 347083 TGAGCGCTGCACCCTAATACATCAGTACTTACAGCTCCAAAGTGAATCAATCTGTCCTGTTGAAA TGAGCGCTGCACCCTAATACATCAGTACTTACGGCTCCAAAGTGAATCAATCTGTCCTGTTGAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:347034..347117 26863196 MeRIP-seq:(Medium) rs980564027 Functional Loss SNV dbSNP153 33..33 33 - - - 72402 RMVar_ID_72402 Human_SNP_ID_590522746 m1A Human chr16 - 352653 352653 352653 CTTCGGCGCTCTGGCTCGGGCTCTGGCTCGGGAGGCGATCGTGGCCGCTGCCGCCGCCAGAGCCG CTTCGGCGCTCTGGCTCGGGCTCTGGCTCGGGTGGCGATCGTGGCCGCTGCCGCCGCCAGAGCCG T A AXIN1 Ensembl:ENSG00000103126 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:352566..352700 26863410 MeRIP-seq:(Medium) rs986618914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473931,Human_RBP_ID_4393383,Human_RBP_ID_5237138,Human_RBP_ID_5465169 72403 RMVar_ID_72403 Human_SNP_ID_590522747 m1A Human chr16 - 352653 352653 352653 CTTCGGCGCTCTGGCTCGGGCTCTGGCTCGGGAGGCGATCGTGGCCGCTGCCGCCGCCAGAGCCG CTTCGGCGCTCTGGCTCGGGCTCTGGCTCGGGGGGCGATCGTGGCCGCTGCCGCCGCCAGAGCCG T C AXIN1 Ensembl:ENSG00000103126 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:352566..352700 26863410 MeRIP-seq:(Medium) rs986618914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473931,Human_RBP_ID_4393383,Human_RBP_ID_5237138,Human_RBP_ID_5465169 72404 RMVar_ID_72404 Human_SNP_ID_590522926 m1A Human chr16 + 353037 353037 353037 GGGAGTAAGGCGGGGCCCGCCTCGAGCAGAAGAGGTAAAGAGCGTGGGGCGGGGCCTCCGGCGCG GGGAGTAAGGCGGGGCCCGCCTCGAGCAGAAGCGGTAAAGAGCGTGGGGCGGGGCCTCCGGCGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:352988..353308 26863196 MeRIP-seq:(Medium) rs1215124165 Functional Loss SNV dbSNP153 33..33 33 - - - 72405 RMVar_ID_72405 Human_SNP_ID_590522927 m1A Human chr16 + 353037 353037 353037 GGGAGTAAGGCGGGGCCCGCCTCGAGCAGAAGAGGTAAAGAGCGTGGGGCGGGGCCTCCGGCGCG GGGAGTAAGGCGGGGCCCGCCTCGAGCAGAAGTGGTAAAGAGCGTGGGGCGGGGCCTCCGGCGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:352988..353308 26863196 MeRIP-seq:(Medium) rs1215124165 Functional Loss SNV dbSNP153 33..33 33 - - - 72406 RMVar_ID_72406 Human_SNP_ID_590525728 m1A Human chr16 - 362184 362182 362184 GGTCCAGGGAGCAAGGCCTCGGGAGGGGCCTCAGGGGGCTTGTGAGACGGGACTGTGTGAGCACG GGTCCAGGGAGCAAGGCCTCGGGAGGGGCCTC__GGGGCTTGTGAGACGGGACTGTGTGAGCACG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:362177..362304 26863196 MeRIP-seq:(Medium) rs1470931531 Functional Loss DEL dbSNP153 33..34 33 - - - 72407 RMVar_ID_72407 Human_SNP_ID_590525729 m1A Human chr16 - 362184 362184 362184 GGTCCAGGGAGCAAGGCCTCGGGAGGGGCCTCAGGGGGCTTGTGAGACGGGACTGTGTGAGCACG GGTCCAGGGAGCAAGGCCTCGGGAGGGGCCTCGGGGGGCTTGTGAGACGGGACTGTGTGAGCACG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:362177..362304 26863196 MeRIP-seq:(Medium) rs1326575368 Functional Loss SNV dbSNP153 33..33 33 - - - 72408 RMVar_ID_72408 Human_SNP_ID_590527748 m1A Human chr16 - 367727 367727 367727 CTATGTGGCGGAGCTGATCCAGCAGCTGCAGCAGCAGGCACTGTCAGAGCCGGCGGTGGTGCAGA CTATGTGGCGGAGCTGATCCAGCAGCTGCAGCCGCAGGCACTGTCAGAGCCGGCGGTGGTGCAGA T G MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:367677..368370 32194978 MeRIP-seq:(Medium) rs566028789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760604,Human_RBP_ID_1088650,Human_RBP_ID_5114385,Human_RBP_ID_17652842,Human_RBP_ID_18679338,Human_RBP_ID_18984684 Human_Splice_Rec_1653604,Human_Splice_Rec_1653612,Human_Splice_Rec_1653620,Human_Splice_Rec_1653626,Human_Splice_Rec_1653632,Human_Splice_Rec_1653638,Human_Splice_Rec_1653646,Human_Splice_Rec_1653654 Human_miRNA_ID_2512623,Human_miRNA_ID_3055445 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_94257,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333,RMVar_hsa_circ_175331 72409 RMVar_ID_72409 Human_SNP_ID_590528010 m1A Human chr16 - 368362 368359 368362 GGAGGCAGAGTGGGTGGGCCTCACGCTGGAGGAGGCCATTGAGAAGCAGAGACTTTTGGAGGAGA GGAGGCAGAGTGGGTGGGCCTCACGCTGGAGG___CCATTGAGAAGCAGAGACTTTTGGAGGAGA GCCT G MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:367581..368601 26863196 MeRIP-seq:(Medium) rs762148892 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3946858,Human_RBP_ID_5113761,Human_RBP_ID_9285520,Human_RBP_ID_9371986,Human_RBP_ID_17652843,Human_RBP_ID_18982741,Human_RBP_ID_22440790,Human_RBP_ID_22581530,Human_RBP_ID_22651265,Human_RBP_ID_26328338 Human_Splice_Rec_1653602,Human_Splice_Rec_1653603,Human_Splice_Rec_1653610,Human_Splice_Rec_1653611,Human_Splice_Rec_1653618,Human_Splice_Rec_1653619,Human_Splice_Rec_1653624,Human_Splice_Rec_1653625,Human_Splice_Rec_1653630,Human_Splice_Rec_1653631,Human_Splice_Rec_1653636,Human_Splice_Rec_1653637,Human_Splice_Rec_1653644,Human_Splice_Rec_1653645,Human_Splice_Rec_1653652,Human_Splice_Rec_1653653,Human_Splice_Rec_1653660,Human_Splice_Rec_1653666 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_94257,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333,RMVar_hsa_circ_175334,RMVar_hsa_circ_175331 72410 RMVar_ID_72410 Human_SNP_ID_590528014 m1A Human chr16 - 368362 368362 368362 GGAGGCAGAGTGGGTGGGCCTCACGCTGGAGGAGGCCATTGAGAAGCAGAGACTTTTGGAGGAGA GGAGGCAGAGTGGGTGGGCCTCACGCTGGAGGCGGCCATTGAGAAGCAGAGACTTTTGGAGGAGA T G MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:367581..368601 26863196 MeRIP-seq:(Medium) rs1332087974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3946858,Human_RBP_ID_5113761,Human_RBP_ID_9285520,Human_RBP_ID_9371986,Human_RBP_ID_17652843,Human_RBP_ID_18982741,Human_RBP_ID_22440790,Human_RBP_ID_22581530,Human_RBP_ID_22651265,Human_RBP_ID_26328338 Human_Splice_Rec_1653602,Human_Splice_Rec_1653603,Human_Splice_Rec_1653610,Human_Splice_Rec_1653611,Human_Splice_Rec_1653618,Human_Splice_Rec_1653619,Human_Splice_Rec_1653624,Human_Splice_Rec_1653625,Human_Splice_Rec_1653630,Human_Splice_Rec_1653631,Human_Splice_Rec_1653636,Human_Splice_Rec_1653637,Human_Splice_Rec_1653644,Human_Splice_Rec_1653645,Human_Splice_Rec_1653652,Human_Splice_Rec_1653653,Human_Splice_Rec_1653660,Human_Splice_Rec_1653666 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_94257,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333,RMVar_hsa_circ_175334,RMVar_hsa_circ_175331 72411 RMVar_ID_72411 Human_SNP_ID_590528029 m1A Human chr16 + 368384 368384 368384 CTCAATGGCCTCCTCCAGCGTGAGGCCCACCCACTCTGCCTCCTCCTCTGGGATGGCAAATTCCT CTCAATGGCCTCCTCCAGCGTGAGGCCCACCCGCTCTGCCTCCTCCTCTGGGATGGCAAATTCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:368326..368578 26863196 MeRIP-seq:(Medium) rs1172122692 Functional Loss SNV dbSNP153 33..33 33 - - - 72412 RMVar_ID_72412 Human_SNP_ID_590528032 m1A Human chr16 - 368392 368392 368392 GCCTGCCTAGGAATTTGCCATCCCAGAGGAGGAGGCAGAGTGGGTGGGCCTCACGCTGGAGGAGG GCCTGCCTAGGAATTTGCCATCCCAGAGGAGGGGGCAGAGTGGGTGGGCCTCACGCTGGAGGAGG T C MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:367628..368554 26863410 MeRIP-seq:(Medium) rs1239735564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473949,Human_RBP_ID_3948288,Human_RBP_ID_5113761,Human_RBP_ID_9285520,Human_RBP_ID_9371986,Human_RBP_ID_17653169,Human_RBP_ID_18982741,Human_RBP_ID_22440790,Human_RBP_ID_22581530,Human_RBP_ID_22651265,Human_RBP_ID_26328338 Human_Splice_Rec_1653602,Human_Splice_Rec_1653603,Human_Splice_Rec_1653610,Human_Splice_Rec_1653611,Human_Splice_Rec_1653618,Human_Splice_Rec_1653619,Human_Splice_Rec_1653624,Human_Splice_Rec_1653625,Human_Splice_Rec_1653630,Human_Splice_Rec_1653631,Human_Splice_Rec_1653636,Human_Splice_Rec_1653637,Human_Splice_Rec_1653644,Human_Splice_Rec_1653645,Human_Splice_Rec_1653652,Human_Splice_Rec_1653653,Human_Splice_Rec_1653660,Human_Splice_Rec_1653666 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_94257,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333,RMVar_hsa_circ_175334,RMVar_hsa_circ_175331 72413 RMVar_ID_72413 Human_SNP_ID_590528135 m1A Human chr16 - 368553 368553 368553 GATGCTGCTGCGGCTTGCCCGGCAGGACCCCCAGCTGCACCCCGAGGACCCCGAGCGGCGGGCAG GATGCTGCTGCGGCTTGCCCGGCAGGACCCCCGGCTGCACCCCGAGGACCCCGAGCGGCGGGCAG T C MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:368411..368600 26863196 MeRIP-seq:(Medium) rs968233268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233205,Human_RBP_ID_4368887,Human_RBP_ID_9285521,Human_RBP_ID_18984686,Human_RBP_ID_22440791 Human_Splice_Rec_1653601,Human_Splice_Rec_1653609,Human_Splice_Rec_1653617,Human_Splice_Rec_1653623,Human_Splice_Rec_1653629,Human_Splice_Rec_1653635,Human_Splice_Rec_1653643,Human_Splice_Rec_1653651,Human_Splice_Rec_1653659,Human_Splice_Rec_1653665 Human_miRNA_ID_2013416,Human_miRNA_ID_2685321,Human_miRNA_ID_2759808 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_94257,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333,RMVar_hsa_circ_175334,RMVar_hsa_circ_175331 72414 RMVar_ID_72414 Human_SNP_ID_590528151 m1A Human chr16 + 368580 368580 368580 GCAGCTGGGGGTCCTGCCGGGCAAGCCGCAGCAGCATCCCTCGCTTCAGGTCCATCCCAAACTTG GCAGCTGGGGGTCCTGCCGGGCAAGCCGCAGCGGCATCCCTCGCTTCAGGTCCATCCCAAACTTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:368326..368625 26863196 MeRIP-seq:(Medium) rs760433133 Functional Loss SNV dbSNP153 33..33 33 - - - 72415 RMVar_ID_72415 Human_SNP_ID_590528937 m1A Human chr16 + 370097 370095 370097 TCTTGAACTTGGCCCCATGAGGCCTATAGTGCACGGGAGTGGGCGTCCGCTCCTCCTCCAGGGAG TCTTGAACTTGGCCCCATGAGGCCTATAGTG__CGGGAGTGGGCGTCCGCTCCTCCTCCAGGGAG GCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:369926..370225 32194978 MeRIP-seq:(Medium) rs765324207 Functional Loss DEL dbSNP153 32..33 33 - - - 72416 RMVar_ID_72416 Human_SNP_ID_590528945 m1A Human chr16 + 370124 370104 370125 AGTGCACGGGAGTGGGCGTCCGCTCCTCCTCCAGGGAGCGCAGGTAGTGGCCGGGCAGGCGGGAA AGTGCACGGGAGT_____________________GGAGCGCAGGTAGTGGCCGGGCAGGCGGGAA TGGGCGTCCGCTCCTCCTCCAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:370076..370250 26863196 MeRIP-seq:(Medium) rs1199376528 Functional Loss DEL dbSNP153 14..34 33 - - - 72417 RMVar_ID_72417 Human_SNP_ID_590528953 m1A Human chr16 - 370110 370110 370110 GCCACTACCTGCGCTCCCTGGAGGAGGAGCGGACGCCCACTCCCGTGCACTATAGGCCTCATGGG GCCACTACCTGCGCTCCCTGGAGGAGGAGCGGTCGCCCACTCCCGTGCACTATAGGCCTCATGGG T A MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:369926..370250 32194978 MeRIP-seq:(Medium) rs777670523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473958,Human_RBP_ID_4368903,Human_RBP_ID_18679346,Human_RBP_ID_22441201,Human_RBP_ID_27242069 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333 72418 RMVar_ID_72418 Human_SNP_ID_590529040 m1A Human chr16 - 370208 370207 370208 CCCACCTCCCGCCAGGCTCGCGATGCCTCTACACAAGTATCCCGTGTGGCTCTGGAAGCGGCTGC CCCACCTCCCGCCAGGCTCGCGATGCCTCTAC_CAAGTATCCCGTGTGGCTCTGGAAGCGGCTGC GT G MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:369902..370418;chr16:370026..370250 26863196 MeRIP-seq:(Medium) rs1384590292 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_473959,Human_RBP_ID_1518284,Human_RBP_ID_4368905,Human_RBP_ID_5440582,Human_RBP_ID_9420325,Human_RBP_ID_18679347,Human_RBP_ID_19072566,Human_RBP_ID_22583442 Human_Splice_Rec_1653598,Human_Splice_Rec_1653606,Human_Splice_Rec_1653614,Human_Splice_Rec_1653622,Human_Splice_Rec_1653640,Human_Splice_Rec_1653648,Human_Splice_Rec_1653656,Human_Splice_Rec_1653662 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333 72419 RMVar_ID_72419 Human_SNP_ID_590529041 m1A Human chr16 - 370208 370208 370208 CCCACCTCCCGCCAGGCTCGCGATGCCTCTACACAAGTATCCCGTGTGGCTCTGGAAGCGGCTGC CCCACCTCCCGCCAGGCTCGCGATGCCTCTACGCAAGTATCCCGTGTGGCTCTGGAAGCGGCTGC T C MRPL28 Ensembl:ENSG00000086504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:369902..370418;chr16:370026..370250 26863196 MeRIP-seq:(Medium) rs141083967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473959,Human_RBP_ID_1518284,Human_RBP_ID_4368905,Human_RBP_ID_5440582,Human_RBP_ID_9420325,Human_RBP_ID_18679347,Human_RBP_ID_19072566,Human_RBP_ID_22583442 Human_Splice_Rec_1653598,Human_Splice_Rec_1653606,Human_Splice_Rec_1653614,Human_Splice_Rec_1653622,Human_Splice_Rec_1653640,Human_Splice_Rec_1653648,Human_Splice_Rec_1653656,Human_Splice_Rec_1653662 RMVar_hsa_circ_175332,RMVar_hsa_circ_89910,RMVar_hsa_circ_77578,RMVar_hsa_circ_175333 72420 RMVar_ID_72420 Human_SNP_ID_590529205 m1A Human chr16 - 370421 370421 370421 GGAGGGGCAGGTGGGTGCGGGACAGGGGCCGGAGTGAGAACCGGGGGCCGGGGTAGGGGGTAGCG GGAGGGGCAGGTGGGTGCGGGACAGGGGCCGGGGTGAGAACCGGGGGCCGGGGTAGGGGGTAGCG T C MRPL28 Ensembl:ENSG00000086504 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:370420..370504 26863196 MeRIP-seq:(Medium) rs1244624886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8183859,Human_RBP_ID_9419027 Human_Splice_Rec_1653647 RMVar_hsa_circ_77578,RMVar_hsa_circ_175333 72421 RMVar_ID_72421 Human_SNP_ID_590529881 m1A Human chr16 + 372219 372219 372219 TGCCCACAGAGGCCATAGAGACGCCGGGCAGGAGGTAGAAGGCCCAGCGCTGCCACGAGGTGGGG TGCCCACAGAGGCCATAGAGACGCCGGGCAGGTGGTAGAAGGCCCAGCGCTGCCACGAGGTGGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:372151..372250 32194978 MeRIP-seq:(Medium) rs775685733 Functional Loss SNV dbSNP153 33..33 33 - - - 72422 RMVar_ID_72422 Human_SNP_ID_590531742 m1A Human chr16 + 376387 376387 376387 GTGGTCGGGGCTCGGGGACAGCAGACCAGAGGAGGCATTGAAGCTCTGGTTTTGGCTGCTCTGCA GTGGTCGGGGCTCGGGGACAGCAGACCAGAGGGGGCATTGAAGCTCTGGTTTTGGCTGCTCTGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:376338..376751 26863196 MeRIP-seq:(Medium) rs1350473790 Functional Loss SNV dbSNP153 33..33 33 - - - 72423 RMVar_ID_72423 Human_SNP_ID_590531771 m1A Human chr16 + 376453 376453 376453 AAGGGGCTGGATGGTCACGCTCCGTGGCCTGCAAGCTGCCGAGAGGACAAGGGGTTTGGCTGGAG AAGGGGCTGGATGGTCACGCTCCGTGGCCTGCCAGCTGCCGAGAGGACAAGGGGTTTGGCTGGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:376451..376546 26863196 MeRIP-seq:(Medium) rs1230019374 Functional Loss SNV dbSNP153 33..33 33 - - - 72424 RMVar_ID_72424 Human_SNP_ID_590532324 m1A Human chr16 + 377487 377487 377487 TGACGGAGGCATTGCTTCTCGGTGTGGTGCTCAGCGGCACCCCGACCTGGAAGGAGGGCTGTACC TGACGGAGGCATTGCTTCTCGGTGTGGTGCTCGGCGGCACCCCGACCTGGAAGGAGGGCTGTACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:377439..377766 26863196 MeRIP-seq:(Medium) rs776672573 Functional Loss SNV dbSNP153 33..33 33 - - - 72425 RMVar_ID_72425 Human_SNP_ID_590532373 m1A Human chr16 - 377553 377553 377553 GCACTTCCGTTCCGGCGCCCCTCCGGTCATCAACCCGCTGGGCACCAGCTTCCCGGACGACACCG GCACTTCCGTTCCGGCGCCCCTCCGGTCATCAGCCCGCTGGGCACCAGCTTCCCGGACGACACCG T C PGAP6 Ensembl:ENSG00000129925 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:377503..381741 32194978 MeRIP-seq:(Medium) rs1343171923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4369001,Human_RBP_ID_18189731 Human_Splice_Rec_1653670,Human_Splice_Rec_1653698,Human_Splice_Rec_1653740,Human_Splice_Rec_1653750 Human_miRNA_ID_2052177,Human_miRNA_ID_2052178 RMVar_hsa_circ_269244,RMVar_hsa_circ_18156,RMVar_hsa_circ_378465,RMVar_hsa_circ_175337,RMVar_hsa_circ_115256,RMVar_hsa_circ_175345 72426 RMVar_ID_72426 Human_SNP_ID_590534198 m1A Human chr16 - 381821 381821 381821 GGGCCGGGTAGCGCCGGGCCGAGCGCGGAGCCATGGGCCGGGCTGGCACCGGGACCGGGGGCGAG GGGCCGGGTAGCGCCGGGCCGAGCGCGGAGCCTTGGGCCGGGCTGGCACCGGGACCGGGGGCGAG T A PGAP6 Ensembl:ENSG00000129925 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:381783..381914 26863196 MeRIP-seq:(Medium) rs909174948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234849,Human_RBP_ID_261213,Human_RBP_ID_890949,Human_RBP_ID_3503720,Human_RBP_ID_4392688,Human_RBP_ID_8183884,Human_RBP_ID_17652524,Human_RBP_ID_18418621,Human_RBP_ID_22712794 72427 RMVar_ID_72427 Human_SNP_ID_590534215 m1A Human chr16 - 381857 381857 381857 GCCCGGGCGGCGGCGGGGGCCGGCGGCGCGGGACGCGGGCCGGGTAGCGCCGGGCCGAGCGCGGA GCCCGGGCGGCGGCGGGGGCCGGCGGCGCGGGCCGCGGGCCGGGTAGCGCCGGGCCGAGCGCGGA T G PGAP6 Ensembl:ENSG00000129925 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:381775..381880 26863410 MeRIP-seq:(Medium) rs1175363992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234849,Human_RBP_ID_890949,Human_RBP_ID_3503720,Human_RBP_ID_4392689,Human_RBP_ID_8183885,Human_RBP_ID_9324671,Human_RBP_ID_18418621,Human_RBP_ID_18458913,Human_RBP_ID_22712794 72428 RMVar_ID_72428 Human_SNP_ID_590534224 m1A Human chr16 + 381890 381883 381891 CCCGCGCCGCCGGCCCCCGCCGCCGCCCGGGCAGCCTCTGCCGCCTCCGCCTCTGCCGCCTCCGC CCCGCGCCGCCGGCCCCCGCCGCCGC________CCTCTGCCGCCTCCGCCTCTGCCGCCTCCGC CCCGGGCAG C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:381789..381981 26863410 MeRIP-seq:(Medium) rs1312764509 Functional Loss DEL dbSNP153 27..34 33 - - - 72429 RMVar_ID_72429 Human_SNP_ID_590534229 m1A Human chr16 + 381890 381889 381891 CCCGCGCCGCCGGCCCCCGCCGCCGCCCGGGCAGCCTCTGCCGCCTCCGCCTCTGCCGCCTCCGC CCCGCGCCGCCGGCCCCCGCCGCCGCCCGGGC__CCTCTGCCGCCTCCGCCTCTGCCGCCTCCGC CAG C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:381789..381981 26863410 MeRIP-seq:(Medium) rs1491431945 Functional Loss DEL dbSNP153 33..34 33 - - - 72430 RMVar_ID_72430 Human_SNP_ID_590534233 m1A Human chr16 - 381894 381894 381894 AGAGGCGGAGGCGGCAGAGGCGGAGGCGGCAGAGGCTGCCCGGGCGGCGGCGGGGGCCGGCGGCG AGAGGCGGAGGCGGCAGAGGCGGAGGCGGCAGGGGCTGCCCGGGCGGCGGCGGGGGCCGGCGGCG T C PGAP6 Ensembl:ENSG00000129925 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:381807..381893 26863410 MeRIP-seq:(Medium) rs1398358368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261214,Human_RBP_ID_890949,Human_RBP_ID_3503720,Human_RBP_ID_4392689,Human_RBP_ID_8183885,Human_RBP_ID_9324671,Human_RBP_ID_18418621,Human_RBP_ID_18458913,Human_RBP_ID_22712079 72431 RMVar_ID_72431 Human_SNP_ID_590534433 m1A Human chr16 - 382174 382174 382174 CCTCTCCGTCCTGGGACCCCCGCGATCCCTCCATCCCGCGCCCTCCCTCCAGCGTCCCCCCGGAC CCTCTCCGTCCTGGGACCCCCGCGATCCCTCCCTCCCGCGCCCTCCCTCCAGCGTCCCCCCGGAC T G PGAP6 Ensembl:ENSG00000129925 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:382123..383349 26863196 MeRIP-seq:(Medium) rs1197826820 Functional Loss SNV dbSNP153 33..33 33 - - - 72432 RMVar_ID_72432 Human_SNP_ID_590534435 m1A Human chr16 + 382181 382181 382181 GGGACGCTGGAGGGAGGGCGCGGGATGGAGGGATCGCGGGGGTCCCAGGACGGAGAGGTCGCGCC GGGACGCTGGAGGGAGGGCGCGGGATGGAGGGCTCGCGGGGGTCCCAGGACGGAGAGGTCGCGCC A C Z97634.1 Ensembl:ENSG00000236829 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:382132..382254 26863196 MeRIP-seq:(Medium) rs1251624892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1527113,Human_RBP_ID_3511441,Human_RBP_ID_5247336,Human_RBP_ID_8188184,Human_RBP_ID_8812653,Human_RBP_ID_17189213,Human_RBP_ID_18418622,Human_RBP_ID_19077774,Human_RBP_ID_21973494 72433 RMVar_ID_72433 Human_SNP_ID_590539462 m1A Human chr16 - 397265 397265 397265 TAGCAGGCTCGGGCCCGGGGCCCGCGGGCCGCAGCGCAGCCCCCGCAGCGCGGAGCGCCAGAAGA TAGCAGGCTCGGGCCCGGGGCCCGCGGGCCGCGGCGCAGCCCCCGCAGCGCGGAGCGCCAGAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:397201..397959;chr16:397226..397415;chr16:397201..397992;chr16:397226..397960 26863196 MeRIP-seq:(Medium) rs1260598754 Functional Loss SNV dbSNP153 33..33 33 - - - 72434 RMVar_ID_72434 Human_SNP_ID_590539475 m1A Human chr16 + 397289 397289 397289 GGCTGCGCTGCGGCCCGCGGGCCCCGGGCCCGAGCCTGCTAGTGCGCCACGGCTCGGGTGAGTGG GGCTGCGCTGCGGCCCGCGGGCCCCGGGCCCGTGCCTGCTAGTGCGCCACGGCTCGGGTGAGTGG A T NME4 Ensembl:ENSG00000103202 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:397216..397353 26863410 MeRIP-seq:(Medium) rs1435661495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233402,Human_RBP_ID_474077,Human_RBP_ID_4392691,Human_RBP_ID_5141747,Human_RBP_ID_5236408,Human_RBP_ID_8941292,Human_RBP_ID_9324672,Human_RBP_ID_22441203,Human_RBP_ID_24531152 Human_Splice_Rec_1653775,Human_Splice_Rec_1653785,Human_Splice_Rec_1653791,Human_Splice_Rec_1653801,Human_Splice_Rec_1653809,Human_Splice_Rec_1653829,Human_Splice_Rec_1653837,Human_Splice_Rec_1653847 Human_miRNA_ID_2027442 RMVar_hsa_circ_125945,RMVar_hsa_circ_175347 72435 RMVar_ID_72435 Human_SNP_ID_590539936 m1A Human chr16 + 398100 398100 398100 CTTTGGCTCTGTCCAGATTCTGTGGGACATACAGGGTCTGGGCTCCTCTGGAAACCAGGGACCCG CTTTGGCTCTGTCCAGATTCTGTGGGACATACGGGGTCTGGGCTCCTCTGGAAACCAGGGACCCG A G NME4 Ensembl:ENSG00000103202 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:398098..398336 26863196 MeRIP-seq:(Medium) rs957003882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261220,Human_RBP_ID_889189,Human_RBP_ID_1518337,Human_RBP_ID_3502179,Human_RBP_ID_3946863,Human_RBP_ID_8084327,Human_RBP_ID_8185606,Human_RBP_ID_8231739,Human_RBP_ID_8726011,Human_RBP_ID_8941298,Human_RBP_ID_9325640,Human_RBP_ID_9419529,Human_RBP_ID_12736715,Human_RBP_ID_17876857,Human_RBP_ID_18481554,Human_RBP_ID_18939836,Human_RBP_ID_22651269,Human_RBP_ID_25209996 Human_Splice_Rec_1653855 RMVar_hsa_circ_125945,RMVar_hsa_circ_175347 72436 RMVar_ID_72436 Human_SNP_ID_590539962 m1A Human chr16 + 398158 398158 398158 GGACCCGATGCCGGAGGGTAGCTTGGCTCTGGAGCAGCCTGGGACTATAGGAAGGTGAGGACGTC GGACCCGATGCCGGAGGGTAGCTTGGCTCTGGGGCAGCCTGGGACTATAGGAAGGTGAGGACGTC A G NME4 Ensembl:ENSG00000103202 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:398156..398334 26863196 MeRIP-seq:(Medium) rs1362695452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474083,Human_RBP_ID_818000,Human_RBP_ID_3502179,Human_RBP_ID_8084327,Human_RBP_ID_8187594,Human_RBP_ID_8941299,Human_RBP_ID_9421255,Human_RBP_ID_12736726,Human_RBP_ID_18481554,Human_RBP_ID_21970826,Human_RBP_ID_22739066,Human_RBP_ID_22944524 Human_Splice_Rec_1653855 RMVar_hsa_circ_125945,RMVar_hsa_circ_175347 72437 RMVar_ID_72437 Human_SNP_ID_590540241 m1A Human chr16 - 398937 398937 398937 GAGGCACTGCCACCTCACCCTTTCACGTCCCCACGACCCGGGTTTCCCAGCCAGAGCCCAGGGGT GAGGCACTGCCACCTCACCCTTTCACGTCCCCGCGACCCGGGTTTCCCAGCCAGAGCCCAGGGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:398935..399150 26863410 MeRIP-seq:(Medium) rs570887273 Functional Loss SNV dbSNP153 33..33 33 - - - 72438 RMVar_ID_72438 Human_SNP_ID_590540242 m1A Human chr16 - 398937 398937 398937 GAGGCACTGCCACCTCACCCTTTCACGTCCCCACGACCCGGGTTTCCCAGCCAGAGCCCAGGGGT GAGGCACTGCCACCTCACCCTTTCACGTCCCCCCGACCCGGGTTTCCCAGCCAGAGCCCAGGGGT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:398935..399150 26863410 MeRIP-seq:(Medium) rs570887273 Functional Loss SNV dbSNP153 33..33 33 - - - 72439 RMVar_ID_72439 Human_SNP_ID_590540301 m1A Human chr16 - 399044 399044 399044 GCTGGATCACGTCCCCAACGAGCCGCCGTTGCACGCCATCGGGCTTCACCGCCACCAGGGTCCGC GCTGGATCACGTCCCCAACGAGCCGCCGTTGCGCGCCATCGGGCTTCACCGCCACCAGGGTCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:398964..399128;chr16:398976..399177 26863196 MeRIP-seq:(Medium) rs756481093 Functional Loss SNV dbSNP153 33..33 33 - - - 72440 RMVar_ID_72440 Human_SNP_ID_590540305 m1A Human chr16 + 399048 399048 399048 ACCCTGGTGGCGGTGAAGCCCGATGGCGTGCAACGGCGGCTCGTTGGGGACGTGATCCAGCGCTT ACCCTGGTGGCGGTGAAGCCCGATGGCGTGCAGCGGCGGCTCGTTGGGGACGTGATCCAGCGCTT A G NME4 Ensembl:ENSG00000103202 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:398961..399177;chr16:398953..399162 26863196 MeRIP-seq:(Medium) rs1555494085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126428,Human_RBP_ID_474096,Human_RBP_ID_4369291,Human_RBP_ID_5419355,Human_RBP_ID_9325641,Human_RBP_ID_18189733,Human_RBP_ID_22473692,Human_RBP_ID_26945099 Human_Splice_Rec_1653762,Human_Splice_Rec_1653763,Human_Splice_Rec_1653772,Human_Splice_Rec_1653773,Human_Splice_Rec_1653778,Human_Splice_Rec_1653779,Human_Splice_Rec_1653786,Human_Splice_Rec_1653787,Human_Splice_Rec_1653794,Human_Splice_Rec_1653795,Human_Splice_Rec_1653802,Human_Splice_Rec_1653803,Human_Splice_Rec_1653810,Human_Splice_Rec_1653811,Human_Splice_Rec_1653831,Human_Splice_Rec_1653840,Human_Splice_Rec_1653841,Human_Splice_Rec_1653848,Human_Splice_Rec_1653849,Human_Splice_Rec_1653856,Human_Splice_Rec_1653857 Human_miRNA_ID_3010781 RMVar_hsa_circ_101780,RMVar_hsa_circ_125945,RMVar_hsa_circ_175347,RMVar_hsa_circ_218,RMVar_hsa_circ_41064,RMVar_hsa_circ_175348 72441 RMVar_ID_72441 Human_SNP_ID_590540471 m1A Human chr16 + 399388 399388 399388 CTCCTTACCTCAATGCCACCCAGGCACCAGAGAGCGTCCTTGCCGAGCACTACCAGGACCTGCGG CTCCTTACCTCAATGCCACCCAGGCACCAGAGTGCGTCCTTGCCGAGCACTACCAGGACCTGCGG A T NME4 Ensembl:ENSG00000103202 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:399376..399450 26863196 MeRIP-seq:(Medium) rs1358156082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474112,Human_RBP_ID_1518371,Human_RBP_ID_4392695,Human_RBP_ID_8433835,Human_RBP_ID_9324676,Human_RBP_ID_18161836,Human_RBP_ID_18679452,Human_RBP_ID_18984696,Human_RBP_ID_27242153 Human_Splice_Rec_1653764,Human_Splice_Rec_1653765,Human_Splice_Rec_1653774,Human_Splice_Rec_1653780,Human_Splice_Rec_1653781,Human_Splice_Rec_1653796,Human_Splice_Rec_1653797,Human_Splice_Rec_1653804,Human_Splice_Rec_1653805,Human_Splice_Rec_1653812,Human_Splice_Rec_1653813,Human_Splice_Rec_1653832,Human_Splice_Rec_1653833,Human_Splice_Rec_1653842,Human_Splice_Rec_1653843,Human_Splice_Rec_1653850,Human_Splice_Rec_1653851,Human_Splice_Rec_1653858,Human_Splice_Rec_1653859 RMVar_hsa_circ_101780,RMVar_hsa_circ_125945,RMVar_hsa_circ_175347,RMVar_hsa_circ_218,RMVar_hsa_circ_41064,RMVar_hsa_circ_46323,RMVar_hsa_circ_175348,RMVar_hsa_circ_372190,RMVar_hsa_circ_175349 72442 RMVar_ID_72442 Human_SNP_ID_590540600 m1A Human chr16 + 399635 399635 399635 CCCAACCATTATCTCTCGCTGCAGGTCTGGGAAGGGTACAATGTCGTCCGCGCCTCGAGGGCCAT CCCAACCATTATCTCTCGCTGCAGGTCTGGGACGGGTACAATGTCGTCCGCGCCTCGAGGGCCAT A C NME4 Ensembl:ENSG00000103202 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:399626..399750 32194978 MeRIP-seq:(Medium) rs1339809730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474117,Human_RBP_ID_3948299,Human_RBP_ID_4369324,Human_RBP_ID_5114062,Human_RBP_ID_17883620,Human_RBP_ID_18984699,Human_RBP_ID_22583455,Human_RBP_ID_22651271,Human_RBP_ID_24370100 Human_Splice_Rec_1653766,Human_Splice_Rec_1653782,Human_Splice_Rec_1653788,Human_Splice_Rec_1653798,Human_Splice_Rec_1653806,Human_Splice_Rec_1653814,Human_Splice_Rec_1653834,Human_Splice_Rec_1653844,Human_Splice_Rec_1653852,Human_Splice_Rec_1653860 RMVar_hsa_circ_91713,RMVar_hsa_circ_125945,RMVar_hsa_circ_175347,RMVar_hsa_circ_218,RMVar_hsa_circ_41064,RMVar_hsa_circ_46323,RMVar_hsa_circ_372190,RMVar_hsa_circ_175349,RMVar_hsa_circ_175350 72443 RMVar_ID_72443 Human_SNP_ID_590540919 m1A Human chr16 + 400283 400283 400283 GGGCCCAGCGGGAGATCCAGCTGTGGTTCCAGAGCAGTGAGCTGGTGAGCTGGGCAGACGGGGGC GGGCCCAGCGGGAGATCCAGCTGTGGTTCCAGGGCAGTGAGCTGGTGAGCTGGGCAGACGGGGGC A G NME4 Ensembl:ENSG00000103202 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:400201..400686;chr16:400201..400450 32194978 MeRIP-seq:(Medium) rs1452196311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277544,Human_RBP_ID_474125,Human_RBP_ID_1842529,Human_RBP_ID_4400420,Human_RBP_ID_5141750,Human_RBP_ID_8433845,Human_RBP_ID_17653171,Human_RBP_ID_17690339,Human_RBP_ID_17876888,Human_RBP_ID_18161837,Human_RBP_ID_18437737 Human_Splice_Rec_1653768,Human_Splice_Rec_1653784,Human_Splice_Rec_1653790,Human_Splice_Rec_1653800,Human_Splice_Rec_1653808,Human_Splice_Rec_1653816,Human_Splice_Rec_1653817,Human_Splice_Rec_1653836,Human_Splice_Rec_1653846,Human_Splice_Rec_1653862,Human_Splice_Rec_1653864 Human_miRNA_ID_955134,Human_miRNA_ID_2908160,Human_miRNA_ID_3026999 RMVar_hsa_circ_91713,RMVar_hsa_circ_125945,RMVar_hsa_circ_175347,RMVar_hsa_circ_218,RMVar_hsa_circ_46323,RMVar_hsa_circ_107181,RMVar_hsa_circ_175350,RMVar_hsa_circ_175351 72444 RMVar_ID_72444 Human_SNP_ID_590540997 m1A Human chr16 + 400422 400422 400422 CTCCGTCAGCAAGAACCCAAGCCCACATCCAAACCTGCCTGTCCCAAACCACTTACTTCCCTGTT CTCCGTCAGCAAGAACCCAAGCCCACATCCAACCCTGCCTGTCCCAAACCACTTACTTCCCTGTT A C NME4 Ensembl:ENSG00000103202 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr16:400321..400525;chr16:400226..400467 26863410 MeRIP-seq:(Medium) rs1343617939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474130,Human_RBP_ID_3495199,Human_RBP_ID_5113260,Human_RBP_ID_8433847,Human_RBP_ID_17078070,Human_RBP_ID_17254290,Human_RBP_ID_17369772,Human_RBP_ID_17486441,Human_RBP_ID_17652845,Human_RBP_ID_18938529,Human_RBP_ID_22421675,Human_RBP_ID_26441223,Human_RBP_ID_26945127 Human_miRNA_ID_1302275,Human_miRNA_ID_2058149 RMVar_hsa_circ_91713,RMVar_hsa_circ_125945,RMVar_hsa_circ_175347,RMVar_hsa_circ_107181,RMVar_hsa_circ_175350,RMVar_hsa_circ_175351 72445 RMVar_ID_72445 Human_SNP_ID_590542677 m1A Human chr16 - 404964 404964 404964 CAATCCCAGAGCCGCCTCCTGTGATGAAGGCCACTTTGTCCCTGAGAATAAAAAAGGAGGCTCTT CAATCCCAGAGCCGCCTCCTGTGATGAAGGCCGCTTTGTCCCTGAGAATAAAAAAGGAGGCTCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:404956..405056 26863196 MeRIP-seq:(Medium) rs1384661734 Functional Loss SNV dbSNP153 33..33 33 - - - 72446 RMVar_ID_72446 Human_SNP_ID_590543532 m1A Human chr16 - 407465 407465 407465 CTGGGGGCGCTCGGACGTCCATAGAGAGAGGGAGGCAGCGCCGGCCGGTGGCCCCAGCCAGCTTC CTGGGGGCGCTCGGACGTCCATAGAGAGAGGGTGGCAGCGCCGGCCGGTGGCCCCAGCCAGCTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:407435..407504 26863196 MeRIP-seq:(Medium) rs772933095 Functional Loss SNV dbSNP153 33..33 33 - - - 72447 RMVar_ID_72447 Human_SNP_ID_590543533 m1A Human chr16 - 407465 407465 407465 CTGGGGGCGCTCGGACGTCCATAGAGAGAGGGAGGCAGCGCCGGCCGGTGGCCCCAGCCAGCTTC CTGGGGGCGCTCGGACGTCCATAGAGAGAGGGCGGCAGCGCCGGCCGGTGGCCCCAGCCAGCTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:407435..407504 26863196 MeRIP-seq:(Medium) rs772933095 Functional Loss SNV dbSNP153 33..33 33 - - - 72448 RMVar_ID_72448 Human_SNP_ID_590549750 m1A Human chr16 - 425712 425712 425712 TGGCGGGGGACGGGGGCCGAGGAGGCCGGGGGACGGGGGCCGAGGAGGCCGGAGGCCGCGGAGCC TGGCGGGGGACGGGGGCCGAGGAGGCCGGGGGCCGGGGGCCGAGGAGGCCGGAGGCCGCGGAGCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr16:425626..425950;chr16:425659..425741 26863410 MeRIP-seq:(Medium) rs1188089909 Functional Loss SNV dbSNP153 33..33 33 - - - 72449 RMVar_ID_72449 Human_SNP_ID_590550080 m1A Human chr16 + 426476 426476 426476 GGGGTCCAGCAGCAGCCACCGAGCGCGGGGCGAGGTCGACGTCTTCTCTCCCTTCCCCGCGCCCA GGGGTCCAGCAGCAGCCACCGAGCGCGGGGCGGGGTCGACGTCTTCTCTCCCTTCCCCGCGCCCA A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:426425..426673 26863196 MeRIP-seq:(Medium) rs1268216334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2137183,Human_miRNA_ID_2665971 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355 72450 RMVar_ID_72450 Human_SNP_ID_590550120 m1A Human chr16 + 426554 426554 426554 GGCGCTGGAGCAAGGTCCCGGGTCCCCGCCGCAGCCCTCGGACCTCAGCCAGACCCACCCCCTTC GGCGCTGGAGCAAGGTCCCGGGTCCCCGCCGCTGCCCTCGGACCTCAGCCAGACCCACCCCCTTC A T RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:426504..426617 26863196 MeRIP-seq:(Medium) rs1287008954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2332576,Human_miRNA_ID_2965662 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355 72451 RMVar_ID_72451 Human_SNP_ID_590550127 m1A Human chr16 - 426559 426559 426559 GCTCGGAAGGGGGTGGGTCTGGCTGAGGTCCGAGGGCTGCGGCGGGGACCCGGGACCTTGCTCCA GCTCGGAAGGGGGTGGGTCTGGCTGAGGTCCGCGGGCTGCGGCGGGGACCCGGGACCTTGCTCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:426196..426596 26863196 MeRIP-seq:(Medium) rs1307180823 Functional Loss SNV dbSNP153 33..33 33 - - - 72452 RMVar_ID_72452 Human_SNP_ID_590560992 m1A Human chr16 + 462704 462690 462704 CCCCGGCACCGTCCCTTCCCCAGTCCCCCGGCACCGTCCCTTCCCCAGTCCCTTCCCCAGCACCA CCCCGGCACCGTCCCTTCC______________CCGTCCCTTCCCCAGTCCCTTCCCCAGCACCA CCCAGTCCCCCGGCA C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:462698..462796 26863196 MeRIP-seq:(Medium) rs1254324187 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_17077284,Human_RBP_ID_18938533,Human_RBP_ID_21970828 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_329351,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225 72453 RMVar_ID_72453 Human_SNP_ID_590561003 m1A Human chr16 + 462704 462702 462704 CCCCGGCACCGTCCCTTCCCCAGTCCCCCGGCACCGTCCCTTCCCCAGTCCCTTCCCCAGCACCA CCCCGGCACCGTCCCTTCCCCAGTCCCCCGG__CCGTCCCTTCCCCAGTCCCTTCCCCAGCACCA GCA G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:462698..462796 26863196 MeRIP-seq:(Medium) rs1000947357 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17077284,Human_RBP_ID_18938533,Human_RBP_ID_21970828 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_329351,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225 72454 RMVar_ID_72454 Human_SNP_ID_590561039 m1A Human chr16 + 462792 462792 462792 CCCTTCCCCAGCACCGTCCCTTCCCCAGCACCATCCCTTCCCCAGCACCGTCCCTTCCCCAGCAC CCCTTCCCCAGCACCGTCCCTTCCCCAGCACCCTCCCTTCCCCAGCACCGTCCCTTCCCCAGCAC A C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:462786..462884 26863196 MeRIP-seq:(Medium) rs1486641221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17077284,Human_RBP_ID_21970829 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_329351,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225 72455 RMVar_ID_72455 Human_SNP_ID_590561040 m1A Human chr16 + 462792 462792 462792 CCCTTCCCCAGCACCGTCCCTTCCCCAGCACCATCCCTTCCCCAGCACCGTCCCTTCCCCAGCAC CCCTTCCCCAGCACCGTCCCTTCCCCAGCACCGTCCCTTCCCCAGCACCGTCCCTTCCCCAGCAC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:462786..462884 26863196 MeRIP-seq:(Medium) rs1486641221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17077284,Human_RBP_ID_21970829 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_329351,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225 72456 RMVar_ID_72456 Human_SNP_ID_590570528 m1A Human chr16 - 494827 494786 494827 TGATCCTCCCACCTCTGCAGCCTCGACCTCCCAGGCTCATGTGATCCTCCCACCTCTGCAGCCTC TGATCCTCCCACCTCTGCAGCCTCGACCTCCC_________________________________ GGGGAGGTCGAGGCTGCAGAGGTGGGAGGATCACATGAGCCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:494642..495289 26863196 MeRIP-seq:(Medium) rs1453319446 Functional Loss DEL dbSNP153 33..65 33 - - - 72457 RMVar_ID_72457 Human_SNP_ID_590570547 m1A Human chr16 - 494827 494827 494827 TGATCCTCCCACCTCTGCAGCCTCGACCTCCCAGGCTCATGTGATCCTCCCACCTCTGCAGCCTC TGATCCTCCCACCTCTGCAGCCTCGACCTCCCTGGCTCATGTGATCCTCCCACCTCTGCAGCCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:494642..495289 26863196 MeRIP-seq:(Medium) rs4984880 Functional Loss SNV dbSNP153 33..33 33 - - - 72458 RMVar_ID_72458 Human_SNP_ID_590570548 m1A Human chr16 - 494827 494827 494827 TGATCCTCCCACCTCTGCAGCCTCGACCTCCCAGGCTCATGTGATCCTCCCACCTCTGCAGCCTC TGATCCTCCCACCTCTGCAGCCTCGACCTCCCCGGCTCATGTGATCCTCCCACCTCTGCAGCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:494642..495289 26863196 MeRIP-seq:(Medium) rs4984880 Functional Loss SNV dbSNP153 33..33 33 - - - 72459 RMVar_ID_72459 Human_SNP_ID_590570551 m1A Human chr16 + 494844 494844 494844 AGGATCACATGAGCCTGGGAGGTCGAGGCTGCAGAGGTGGGAGGATCACATGAGCCGGGGAGGTC AGGATCACATGAGCCTGGGAGGTCGAGGCTGCTGAGGTGGGAGGATCACATGAGCCGGGGAGGTC A T RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:494664..495308 26863196 MeRIP-seq:(Medium) rs201399049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475474,Human_RBP_ID_816098,Human_RBP_ID_3503746,Human_RBP_ID_8183908,Human_RBP_ID_12756267,Human_RBP_ID_18418836,Human_RBP_ID_22715197,Human_RBP_ID_22940109 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_93194,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175357,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_272740,RMVar_hsa_circ_175362,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 72460 RMVar_ID_72460 Human_SNP_ID_590574042 m1A Human chr16 + 505615 505615 505615 GCAACACAGCCGCCTGAGGCAGGAGAACCTGCAGCTGGTGCACAGGTGAGCCTGGGCCAGGAGAC GCAACACAGCCGCCTGAGGCAGGAGAACCTGCGGCTGGTGCACAGGTGAGCCTGGGCCAGGAGAC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:505606..505671 26863196 MeRIP-seq:(Medium) rs777345091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5357124,Human_RBP_ID_18984720,Human_RBP_ID_19070287 Human_Splice_Rec_1654042,Human_Splice_Rec_1654043,Human_Splice_Rec_1654068,Human_Splice_Rec_1654069,Human_Splice_Rec_1654090,Human_Splice_Rec_1654091,Human_Splice_Rec_1654112,Human_Splice_Rec_1654138,Human_Splice_Rec_1654139 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175368,RMVar_hsa_circ_345243,RMVar_hsa_circ_175366,RMVar_hsa_circ_292124,RMVar_hsa_circ_175369,RMVar_hsa_circ_341722 72461 RMVar_ID_72461 Human_SNP_ID_590578162 m1A Human chr16 - 519804 519804 519804 TCCCCCATTCTCCTCTTGTTCTCCTGCTCTTCACTGAGCCGCAGCGTCAGCGACTCTATCTCATC TCCCCCATTCTCCTCTTGTTCTCCTGCTCTTCGCTGAGCCGCAGCGTCAGCGACTCTATCTCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:519704..519911;chr16:519686..520199 26863196 MeRIP-seq:(Medium) rs546106364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20128240 Clinvar_Rec_306 72462 RMVar_ID_72462 Human_SNP_ID_590578324 m1A Human chr16 + 520197 520194 520197 TCAAGCTGGAGGCCGAGCAGCGGCGGGGCCGCAGCAGCAGCATGGGCCTGCAGGAGTACCACAGC TCAAGCTGGAGGCCGAGCAGCGGCGGGGCC___GCAGCAGCATGGGCCTGCAGGAGTACCACAGC CGCA C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:520135..520218 26863196 MeRIP-seq:(Medium) rs1490288739 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_1654050,Human_Splice_Rec_1654051,Human_Splice_Rec_1654076,Human_Splice_Rec_1654077,Human_Splice_Rec_1654098,Human_Splice_Rec_1654099 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_79967,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_265064,RMVar_hsa_circ_175370 72463 RMVar_ID_72463 Human_SNP_ID_590578327 m1A Human chr16 + 520197 520197 520197 TCAAGCTGGAGGCCGAGCAGCGGCGGGGCCGCAGCAGCAGCATGGGCCTGCAGGAGTACCACAGC TCAAGCTGGAGGCCGAGCAGCGGCGGGGCCGCGGCAGCAGCATGGGCCTGCAGGAGTACCACAGC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:520135..520218 26863196 MeRIP-seq:(Medium) rs559245815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1654050,Human_Splice_Rec_1654051,Human_Splice_Rec_1654076,Human_Splice_Rec_1654077,Human_Splice_Rec_1654098,Human_Splice_Rec_1654099 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_79967,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_265064,RMVar_hsa_circ_175370 72464 RMVar_ID_72464 Human_SNP_ID_590585163 m1A Human chr16 - 539901 539901 539901 CGGCACCCACAGGGCTCCTCCCTCGGGGCCCTAGGACACCCCCCGGCCCCCAAAAGCCCGGCATC CGGCACCCACAGGGCTCCTCCCTCGGGGCCCTGGGACACCCCCCGGCCCCCAAAAGCCCGGCATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:539897..540044 32194978 MeRIP-seq:(Medium) rs760813922 Functional Loss SNV dbSNP153 33..33 33 - - - 72465 RMVar_ID_72465 Human_SNP_ID_590586667 m1A Human chr16 + 543971 543971 543971 CACAGGCTGGTGGAGCCTGGGAGAGCCAGGGCAGCCTGCGGCCATGCGGCCATGCGGCCGGCGTG CACAGGCTGGTGGAGCCTGGGAGAGCCAGGGCGGCCTGCGGCCATGCGGCCATGCGGCCGGCGTG A G CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:543967..544125 26863196 MeRIP-seq:(Medium) rs1434785628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261238,Human_RBP_ID_890962,Human_RBP_ID_3502218,Human_RBP_ID_5181786,Human_RBP_ID_5237155,Human_RBP_ID_5647466,Human_RBP_ID_8084387,Human_RBP_ID_8183956,Human_RBP_ID_8726053,Human_RBP_ID_8941311,Human_RBP_ID_18161870,Human_RBP_ID_18418853,Human_RBP_ID_18458291,Human_RBP_ID_18481620,Human_RBP_ID_20167888,Human_RBP_ID_22370152,Human_RBP_ID_22415253,Human_RBP_ID_22696960,Human_RBP_ID_22712094,Human_RBP_ID_22738761,Human_RBP_ID_24551852,Human_RBP_ID_27811409 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72466 RMVar_ID_72466 Human_SNP_ID_590586677 m1A Human chr16 + 543990 543990 543990 GGAGAGCCAGGGCAGCCTGCGGCCATGCGGCCATGCGGCCGGCGTGGGGCTGAGGTCCCTGTACA GGAGAGCCAGGGCAGCCTGCGGCCATGCGGCCTTGCGGCCGGCGTGGGGCTGAGGTCCCTGTACA A T CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:543981..544088 26863196 MeRIP-seq:(Medium) rs1300313079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890962,Human_RBP_ID_3503798,Human_RBP_ID_5647466,Human_RBP_ID_8084387,Human_RBP_ID_8183956,Human_RBP_ID_8726053,Human_RBP_ID_8941311,Human_RBP_ID_12769032,Human_RBP_ID_18161870,Human_RBP_ID_18481620,Human_RBP_ID_22415253,Human_RBP_ID_22696960,Human_RBP_ID_22712094,Human_RBP_ID_22738761,Human_RBP_ID_27811409 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72467 RMVar_ID_72467 Human_SNP_ID_590586711 m1A Human chr16 - 544083 544083 544083 GGGGGGTCTACCCTTGTTGCCTCTCTGTGCTGAGCCGCCGGTGCCCGGCCCGTAGATGACTTACT GGGGGGTCTACCCTTGTTGCCTCTCTGTGCTGGGCCGCCGGTGCCCGGCCCGTAGATGACTTACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:543950..544086 26863196 MeRIP-seq:(Medium) rs369439799 Functional Loss SNV dbSNP153 33..33 33 - - - 72468 RMVar_ID_72468 Human_SNP_ID_590586980 m1A Human chr16 + 544743 544718 544743 CCCCACGTCGCCTCCCCCACGTCGCCTCCCCCACGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC CCCCACGT_________________________CGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC TCGCCTCCCCCACGTCGCCTCCCCCA T CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:544694..544914 26863196 MeRIP-seq:(Medium) rs1567146020 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_3503805,Human_RBP_ID_9324701,Human_RBP_ID_12769064,Human_RBP_ID_17371597,Human_RBP_ID_18189737,Human_RBP_ID_18938561,Human_RBP_ID_24413615,Human_RBP_ID_26779907,Human_RBP_ID_27837636 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72469 RMVar_ID_72469 Human_SNP_ID_590587006 m1A Human chr16 + 544743 544732 544743 CCCCACGTCGCCTCCCCCACGTCGCCTCCCCCACGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC CCCCACGTCGCCTCCCCCACGT___________CGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC TCGCCTCCCCCA T CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:544694..544914 26863196 MeRIP-seq:(Medium) rs1567146074 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_3503805,Human_RBP_ID_9324701,Human_RBP_ID_12769064,Human_RBP_ID_17371597,Human_RBP_ID_18189737,Human_RBP_ID_18938561,Human_RBP_ID_24413615,Human_RBP_ID_26779907,Human_RBP_ID_27837636 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72470 RMVar_ID_72470 Human_SNP_ID_590587012 m1A Human chr16 + 544743 544735 544743 CCCCACGTCGCCTCCCCCACGTCGCCTCCCCCACGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC CCCCACGTCGCCTCCCCCACGTCGC________CGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC CCTCCCCCA C CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:544694..544914 26863196 MeRIP-seq:(Medium) rs770950806 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_3503805,Human_RBP_ID_9324701,Human_RBP_ID_12769064,Human_RBP_ID_17371597,Human_RBP_ID_18189737,Human_RBP_ID_18938561,Human_RBP_ID_24413615,Human_RBP_ID_26779907,Human_RBP_ID_27837636 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72471 RMVar_ID_72471 Human_SNP_ID_590587016 m1A Human chr16 - 544763 544735 544763 GACGACGTGGGGGAGACGACGTGGGGGAGGCGACGTGGGGGAGGCGACGACGTGGGGGAGGCGAC GACGACGTGGGGGAGACGACGTGGGGGAGGCG____________________________GCGAC CCTCCCCCACGTCGTCGCCTCCCCCACGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:544647..544891 26863196 MeRIP-seq:(Medium) rs1567146108 Functional Loss DEL dbSNP153 33..60 33 - - - 72472 RMVar_ID_72472 Human_SNP_ID_590587022 m1A Human chr16 - 544737 544737 544737 GAGGCGACGTGGGGGAGGCGACGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCG GAGGCGACGTGGGGGAGGCGACGACGTGGGGGGGGCGACGTGGGGGAGGCGACGTGGGGGAGGCG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:544685..544834 26863196 MeRIP-seq:(Medium) rs62034760 Functional Loss SNV dbSNP153 33..33 33 - - - 72473 RMVar_ID_72473 Human_SNP_ID_590587023 m1A Human chr16 - 544737 544737 544737 GAGGCGACGTGGGGGAGGCGACGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCG GAGGCGACGTGGGGGAGGCGACGACGTGGGGGCGGCGACGTGGGGGAGGCGACGTGGGGGAGGCG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:544685..544834 26863196 MeRIP-seq:(Medium) rs62034760 Functional Loss SNV dbSNP153 33..33 33 - - - 72474 RMVar_ID_72474 Human_SNP_ID_590587030 m1A Human chr16 + 544743 544743 544743 CCCCACGTCGCCTCCCCCACGTCGCCTCCCCCACGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC CCCCACGTCGCCTCCCCCACGTCGCCTCCCCCCCGTCGTCGCCTCCCCCACGTCGCCTCCCCCAC A C CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:544694..544914 26863196 MeRIP-seq:(Medium) rs62034762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503805,Human_RBP_ID_9324701,Human_RBP_ID_12769064,Human_RBP_ID_17371597,Human_RBP_ID_18189737,Human_RBP_ID_18938561,Human_RBP_ID_24413615,Human_RBP_ID_26779907,Human_RBP_ID_27837636 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 72475 RMVar_ID_72475 Human_SNP_ID_590587079 m1A Human chr16 - 544782 544782 544782 GAGGCGACGTGGGGGAGACGACGACGTGGGGGAGACGACGTGGGGGAGGCGACGTGGGGGAGGCG GAGGCGACGTGGGGGAGACGACGACGTGGGGGGGACGACGTGGGGGAGGCGACGTGGGGGAGGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:544609..544888 26863410 MeRIP-seq:(Medium) rs1380827847 Functional Loss SNV dbSNP153 33..33 33 - - - 72476 RMVar_ID_72476 Human_SNP_ID_590587080 m1A Human chr16 - 544782 544782 544782 GAGGCGACGTGGGGGAGACGACGACGTGGGGGAGACGACGTGGGGGAGGCGACGTGGGGGAGGCG GAGGCGACGTGGGGGAGACGACGACGTGGGGGCGACGACGTGGGGGAGGCGACGTGGGGGAGGCG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:544609..544888 26863410 MeRIP-seq:(Medium) rs1380827847 Functional Loss SNV dbSNP153 33..33 33 - - - 72477 RMVar_ID_72477 Human_SNP_ID_590587127 m1A Human chr16 - 544827 544814 544827 GGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGACG GGGGAGGCGACGTGGGGGAGGCGACGTGGGGG_____________GAGGCGACGTGGGGGAGACG CCCCCACGTCGCCT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:544749..544831 26863410 MeRIP-seq:(Medium) rs1225285531 Functional Loss DEL dbSNP153 33..45 33 - - - 72478 RMVar_ID_72478 Human_SNP_ID_590587136 m1A Human chr16 - 544827 544827 544827 GGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGGCGACGTGGGGGAGACG GGGGAGGCGACGTGGGGGAGGCGACGTGGGGGGGGCGACGTGGGGGAGGCGACGTGGGGGAGACG T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:544749..544831 26863410 MeRIP-seq:(Medium) rs1222992167 Functional Loss SNV dbSNP153 33..33 33 - - - 72479 RMVar_ID_72479 Human_SNP_ID_590587903 m1A Human chr16 + 546897 546897 546897 TGTGCGCTGCACCTTCCTGAACCCGGCCGGCCAGCGCCAGTGCTCCATCTGCGAGGCTCCCCGGC TGTGCGCTGCACCTTCCTGAACCCGGCCGGCCGGCGCCAGTGCTCCATCTGCGAGGCTCCCCGGC A G CAPN15 Ensembl:ENSG00000103326 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:546851..546957 26863196 MeRIP-seq:(Medium) rs750099106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233454,Human_RBP_ID_8252239,Human_RBP_ID_12769154,Human_RBP_ID_18163168,Human_RBP_ID_22738073,Human_RBP_ID_27837639 Human_Splice_Rec_1654154,Human_Splice_Rec_1654178,Human_Splice_Rec_1654192 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376,RMVar_hsa_circ_357762 72480 RMVar_ID_72480 Human_SNP_ID_590587990 m1A Human chr16 - 547057 547057 547057 TTGAGGACTGGCAGGAAGGCAGCCCCAGGCGCAGGCTCCGGGGTGAAGCCGCACACCTCGCAGGC TTGAGGACTGGCAGGAAGGCAGCCCCAGGCGCTGGCTCCGGGGTGAAGCCGCACACCTCGCAGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:540359..553705 32194978 MeRIP-seq:(Medium) rs1162865507 Functional Loss SNV dbSNP153 33..33 33 - - - 72481 RMVar_ID_72481 Human_SNP_ID_590588406 m1A Human chr16 + 547749 547749 547749 GCGGCTGAGTGTGCTGGAGGAAGAGGCCACGGAGGGTGGCACCAGCCGCGTAGAGGCCGGCAGCT GCGGCTGAGTGTGCTGGAGGAAGAGGCCACGGGGGGTGGCACCAGCCGCGTAGAGGCCGGCAGCT A G CAPN15 Ensembl:ENSG00000103326 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:547701..547808 26863196 MeRIP-seq:(Medium) rs1183605543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890965 Human_miRNA_ID_2027444,Human_miRNA_ID_2052179,Human_miRNA_ID_2465038 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376,RMVar_hsa_circ_357762 72482 RMVar_ID_72482 Human_SNP_ID_590588407 m1A Human chr16 + 547749 547749 547749 GCGGCTGAGTGTGCTGGAGGAAGAGGCCACGGAGGGTGGCACCAGCCGCGTAGAGGCCGGCAGCT GCGGCTGAGTGTGCTGGAGGAAGAGGCCACGGTGGGTGGCACCAGCCGCGTAGAGGCCGGCAGCT A T CAPN15 Ensembl:ENSG00000103326 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:547701..547808 26863196 MeRIP-seq:(Medium) rs1183605543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890965 Human_miRNA_ID_2027444,Human_miRNA_ID_2052179,Human_miRNA_ID_2465038 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376,RMVar_hsa_circ_357762 72483 RMVar_ID_72483 Human_SNP_ID_590588411 m1A Human chr16 + 547757 547757 547757 GTGTGCTGGAGGAAGAGGCCACGGAGGGTGGCACCAGCCGCGTAGAGGCCGGCAGCTCCACCTCG GTGTGCTGGAGGAAGAGGCCACGGAGGGTGGCGCCAGCCGCGTAGAGGCCGGCAGCTCCACCTCG A G CAPN15 Ensembl:ENSG00000103326 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:547751..547984 26863196 MeRIP-seq:(Medium) rs772314259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2052179 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376,RMVar_hsa_circ_357762 72484 RMVar_ID_72484 Human_SNP_ID_590588539 m1A Human chr16 + 547959 547959 547959 CGGCTGCTCCAAACTGCACGGCTTCCAGGAGCATGGCGAGCCCCCCACCCACTGCCCCGACTGTG CGGCTGCTCCAAACTGCACGGCTTCCAGGAGCGTGGCGAGCCCCCCACCCACTGCCCCGACTGTG A G CAPN15 Ensembl:ENSG00000103326 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:547676..548084 26863196 MeRIP-seq:(Medium) rs1472984348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22203511 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376,RMVar_hsa_circ_357762 72485 RMVar_ID_72485 Human_SNP_ID_590589943 m1A Human chr16 - 550800 550800 550800 CGGGGCACCCTCACCGACCGGGGCCCTCACCGACCGGGACCCTCACCGACCGGGACCCTCACCGG CGGGGCACCCTCACCGACCGGGGCCCTCACCGCCCGGGACCCTCACCGACCGGGACCCTCACCGG T G Z97986.1 Ensembl:ENSG00000261691 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:550782..550866 26863410 MeRIP-seq:(Medium) rs1228540692 Functional Loss SNV dbSNP153 33..33 33 - - - 72486 RMVar_ID_72486 Human_SNP_ID_590589975 m1A Human chr16 - 550833 550833 550833 ACCGGGACCCTCACCGACCGGGGCCATCACCGACGGGGCACCCTCACCGACCGGGGCCCTCACCG ACCGGGACCCTCACCGACCGGGGCCATCACCGGCGGGGCACCCTCACCGACCGGGGCCCTCACCG T C Z97986.1 Ensembl:ENSG00000261691 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:550704..550884 26863410 MeRIP-seq:(Medium) rs1455901952 Functional Loss SNV dbSNP153 33..33 33 - - - 72487 RMVar_ID_72487 Human_SNP_ID_590591231 m1A Human chr16 + 552679 552679 552679 CGCCGGGCCACGTGCTGGCTGTGTACAGCTCGAGGCTGGTCATGGTGGAGCCCGTGGAAGCCCAG CGCCGGGCCACGTGCTGGCTGTGTACAGCTCGGGGCTGGTCATGGTGGAGCCCGTGGAAGCCCAG A G Z97986.1 Ensembl:ENSG00000261691 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1332704438 Functional Loss SNV dbSNP153 33..33 33 - - - 72488 RMVar_ID_72488 Human_SNP_ID_590591712 m1A Human chr16 - 553494 553494 553494 GGCATGGTGGTCACAGCGGTCGGGGCCCATGCAGACCGGCGACCTCTGGCGTGAGTGGGGGGCTG GGCATGGTGGTCACAGCGGTCGGGGCCCATGCGGACCGGCGACCTCTGGCGTGAGTGGGGGGCTG T C Z97986.1 Ensembl:ENSG00000261691 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:553455..553650;chr16:553452..553630 26863196 MeRIP-seq:(Medium) rs759450804 Functional Loss SNV dbSNP153 33..33 33 - - - 72489 RMVar_ID_72489 Human_SNP_ID_590591713 m1A Human chr16 - 553494 553494 553494 GGCATGGTGGTCACAGCGGTCGGGGCCCATGCAGACCGGCGACCTCTGGCGTGAGTGGGGGGCTG GGCATGGTGGTCACAGCGGTCGGGGCCCATGCCGACCGGCGACCTCTGGCGTGAGTGGGGGGCTG T G Z97986.1 Ensembl:ENSG00000261691 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:553455..553650;chr16:553452..553630 26863196 MeRIP-seq:(Medium) rs759450804 Functional Loss SNV dbSNP153 33..33 33 - - - 72490 RMVar_ID_72490 Human_SNP_ID_590597963 m1A Human chr16 - 570037 570037 570037 GCGGCGGGGTCCGGATGGGGTTGGGGACCCCGATGGGCGGGCCCGGGCAGACGACGGCGCTCGCT GCGGCGGGGTCCGGATGGGGTTGGGGACCCCGGTGGGCGGGCCCGGGCAGACGACGGCGCTCGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:570017..570147 26863196 MeRIP-seq:(Medium) rs1188989191 Functional Loss SNV dbSNP153 33..33 33 - - - 72491 RMVar_ID_72491 Human_SNP_ID_590599717 m1A Human chr16 + 574151 574151 574151 CAGCGGGCTGCTGGTGGGACGGTGGGTGCCGGAGCAGAGCAGCGCCGTGGTCCTGGCGGTCCTGC CAGCGGGCTGCTGGTGGGACGGTGGGTGCCGGGGCAGAGCAGCGCCGTGGTCCTGGCGGTCCTGC A G PIGQ,Z98883.1 Ensembl:ENSG00000007541,Ensembl:ENSG00000282907 Protein coding,lincRNA CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:574089..575960 32194978 MeRIP-seq:(Medium) rs753650660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816342,Human_RBP_ID_893218,Human_RBP_ID_3946880,Human_RBP_ID_4376026,Human_RBP_ID_9324714 Human_Splice_Rec_1654210,Human_Splice_Rec_1654214,Human_Splice_Rec_1654236,Human_Splice_Rec_1654238,Human_Splice_Rec_1654258,Human_Splice_Rec_1654264,Human_Splice_Rec_1654286,Human_Splice_Rec_1654304,Human_Splice_Rec_1654308,Human_Splice_Rec_1654442,Human_Splice_Rec_1654446 Human_miRNA_ID_3173142,Human_miRNA_ID_3203607,Human_miRNA_ID_3210631 Clinvar_Rec_307 72492 RMVar_ID_72492 Human_SNP_ID_590601328 m1A Human chr16 - 578029 578029 578029 GAGCCCTCGGCCCCAAACACGTGGACGCACTGAGGCCTGGCAGACCCTGATTCGGCTCCAGCCCT GAGCCCTCGGCCCCAAACACGTGGACGCACTGTGGCCTGGCAGACCCTGATTCGGCTCCAGCCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:578022..578351 26863196 MeRIP-seq:(Medium) rs1285310055 Functional Loss SNV dbSNP153 33..33 33 - - - 72493 RMVar_ID_72493 Human_SNP_ID_590601956 m1A Human chr16 - 579350 579350 579350 CTGTGGCCCAGGGAAGCTCTGCGCTGCTTCAGAGCCCCACGTGCAGCCCACACCGCAGACTTATC CTGTGGCCCAGGGAAGCTCTGCGCTGCTTCAGCGCCCCACGTGCAGCCCACACCGCAGACTTATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:579344..579442 26863196 MeRIP-seq:(Medium) rs1426282600 Functional Loss SNV dbSNP153 33..33 33 - - - 72494 RMVar_ID_72494 Human_SNP_ID_590602579 m1A Human chr16 - 580974 580974 580974 ACCCAGGGCCAGCTGCCCAATACGCAGCACTTACCCGCCAGCCTGTAGGGCCGGCAGAGCCGAAG ACCCAGGGCCAGCTGCCCAATACGCAGCACTTCCCCGCCAGCCTGTAGGGCCGGCAGAGCCGAAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:580453..581326 32194978 MeRIP-seq:(Medium) rs1275200439 Functional Loss SNV dbSNP153 33..33 33 - - - 72495 RMVar_ID_72495 Human_SNP_ID_590603673 m1A Human chr16 - 583460 583460 583460 GGGTGCCTGGGACTGGGGGGTTCATCCTGGCAAGGTCCCTCCACCCCCACAGCCAGGGCAGAGCC GGGTGCCTGGGACTGGGGGGTTCATCCTGGCAGGGTCCCTCCACCCCCACAGCCAGGGCAGAGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:583448..583585 26863196 MeRIP-seq:(Medium) rs750773414 Functional Loss SNV dbSNP153 33..33 33 - - - 72496 RMVar_ID_72496 Human_SNP_ID_590603700 m1A Human chr16 + 583513 583513 583513 TCCCAGGCACCCTCTAGCTCCCTCAGCCGAACAGCACCCTGCATCTGGGGGATTGAAGCAGTCGC TCCCAGGCACCCTCTAGCTCCCTCAGCCGAACGGCACCCTGCATCTGGGGGATTGAAGCAGTCGC A G PIGQ Ensembl:ENSG00000007541 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:582614..584086 32194978 MeRIP-seq:(Medium) rs150633767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476733,Human_RBP_ID_890978,Human_RBP_ID_17078075 72497 RMVar_ID_72497 Human_SNP_ID_590603957 m1A Human chr16 + 583946 583946 583946 GCGGGTGTTCCCTGTGAGCCCGAGTCCGCTTCAGGAGGGGAGCCTGCAGGTGCCGGCTGGTGAGG GCGGGTGTTCCCTGTGAGCCCGAGTCCGCTTCGGGAGGGGAGCCTGCAGGTGCCGGCTGGTGAGG A G PIGQ Ensembl:ENSG00000007541 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:583898..584033 26863196 MeRIP-seq:(Medium) rs866232852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476743,Human_RBP_ID_4392708,Human_RBP_ID_26444630 72498 RMVar_ID_72498 Human_SNP_ID_590605667 m1A Human chr16 + 588831 588831 588831 TTACTTACGACTGTAACAGCGCTACTGAACGCAGAGCACGTATCACAAAGCTCACCCGTTCCGAG TTACTTACGACTGTAACAGCGCTACTGAACGCGGAGCACGTATCACAAAGCTCACCCGTTCCGAG A G lnc-RAB40C-1 RNACentral:URS00008C28AF lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:588825..589034 26863196 MeRIP-seq:(Medium) rs992155536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12769357 72499 RMVar_ID_72499 Human_SNP_ID_590605685 m1A Human chr16 + 588879 588877 588879 AGCTCACCCGTTCCGAGTGAGTAACTTCACCGAGAGAGGCAGGACCATCCCCACGACGGTAGGAC AGCTCACCCGTTCCGAGTGAGTAACTTCACC__GAGAGGCAGGACCATCCCCACGACGGTAGGAC CGA C lnc-RAB40C-1 RNACentral:URS00008C28AF lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:588838..588988 26863196 MeRIP-seq:(Medium) rs1481164366 Functional Loss DEL dbSNP153 32..33 33 - - - 72500 RMVar_ID_72500 Human_SNP_ID_590606045 m1A Human chr16 + 589755 589755 589755 TCGAACCAATGGTTCCGGGAAAGCAGGAGGCGAGTGGCCAATGGCGACGGCGATGAGGCAGGCGT TCGAACCAATGGTTCCGGGAAAGCAGGAGGCGGGTGGCCAATGGCGACGGCGATGAGGCAGGCGT A G RAB40C Ensembl:ENSG00000197562 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:589740..589976 26863196 MeRIP-seq:(Medium) rs923674865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3506109,Human_RBP_ID_8186658 RMVar_hsa_circ_175383,RMVar_hsa_circ_119090 72501 RMVar_ID_72501 Human_SNP_ID_590606314 m1A Human chr16 - 590332 590332 590332 CGTCGCTGTCGCCCACCAGCAGGAACTTGAGCAGGTAGTCGTAGCTCTTCACCGGACTGCCCTGC CGTCGCTGTCGCCCACCAGCAGGAACTTGAGCCGGTAGTCGTAGCTCTTCACCGGACTGCCCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:590043..590391 26863196 MeRIP-seq:(Medium) rs1025699962 Functional Loss SNV dbSNP153 33..33 33 - - - 72502 RMVar_ID_72502 Human_SNP_ID_590606570 m1A Human chr16 + 590909 590909 590909 GTGTCATGGGTGCAGGATCTGGGGTCTGGGAGAAGGTGTCATAGGTCCGAGGGAAGGTGTCATGG GTGTCATGGGTGCAGGATCTGGGGTCTGGGAGGAGGTGTCATAGGTCCGAGGGAAGGTGTCATGG A G RAB40C Ensembl:ENSG00000197562 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:590829..591143 26863196 MeRIP-seq:(Medium) rs1362673987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2478877,Human_RBP_ID_3502248,Human_RBP_ID_5087911,Human_RBP_ID_5316407,Human_RBP_ID_5357150,Human_RBP_ID_8084416,Human_RBP_ID_8183984,Human_RBP_ID_8941313,Human_RBP_ID_9325671,Human_RBP_ID_9353148,Human_RBP_ID_9419054,Human_RBP_ID_18411316,Human_RBP_ID_18938569,Human_RBP_ID_22712849,Human_RBP_ID_23274697,Human_RBP_ID_24551831,Human_RBP_ID_26769043,Human_RBP_ID_26779921 RMVar_hsa_circ_175383,RMVar_hsa_circ_119090 72503 RMVar_ID_72503 Human_SNP_ID_590618187 m1A Human chr16 - 627728 627728 627728 CAGGTGTGAGGAAAGCCCGGCGCTTCTGAGGCAGCTGTGTGGACAGTCTCCACGTAGGCGGCACT CAGGTGTGAGGAAAGCCCGGCGCTTCTGAGGCGGCTGTGTGGACAGTCTCCACGTAGGCGGCACT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:627679..627929 32194978 MeRIP-seq:(Medium) rs760011767 Functional Loss SNV dbSNP153 33..33 33 - - - 72504 RMVar_ID_72504 Human_SNP_ID_590621361 m1A Human chr16 - 634601 634601 634601 AGCCAACAACAAATGCCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCA AGCCAACAACAAATGCCTGATCTTCCGGAAAACCTAAGCCCCTCCTTCACCCCCGCACACCTGCA T G METTL26 Ensembl:ENSG00000130731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:634491..634700 26863196 MeRIP-seq:(Medium) rs775503262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478098,Human_RBP_ID_5113267,Human_RBP_ID_8437130,Human_RBP_ID_17370469,Human_RBP_ID_17652846,Human_RBP_ID_18682525,Human_RBP_ID_22941094,Human_RBP_ID_26809786 Human_Splice_Rec_1654570,Human_Splice_Rec_1654574,Human_Splice_Rec_1654582,Human_Splice_Rec_1654592,Human_Splice_Rec_1654596,Human_Splice_Rec_1654602,Human_Splice_Rec_1654610,Human_Splice_Rec_1654620,Human_Splice_Rec_1654626,Human_Splice_Rec_1654634 Human_miRNA_ID_2390726,Human_miRNA_ID_2591970 RMVar_hsa_circ_81871,RMVar_hsa_circ_118232,RMVar_hsa_circ_116152,RMVar_hsa_circ_175388,RMVar_hsa_circ_175389,RMVar_hsa_circ_175390 72505 RMVar_ID_72505 Human_SNP_ID_590621451 m1A Human chr16 - 634795 634795 634795 GCCATGACTCCATCTCCCCACCCTCTGCAGGAACCCAGAATGGGGGCTTCGGGACACAGCCCTCC GCCATGACTCCATCTCCCCACCCTCTGCAGGAGCCCAGAATGGGGGCTTCGGGACACAGCCCTCC T C METTL26 Ensembl:ENSG00000130731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:634692..635081 32194978 MeRIP-seq:(Medium) rs1218805034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478100,Human_RBP_ID_18162827,Human_RBP_ID_18984762 Human_Splice_Rec_1654568,Human_Splice_Rec_1654569,Human_Splice_Rec_1654572,Human_Splice_Rec_1654573,Human_Splice_Rec_1654580,Human_Splice_Rec_1654581,Human_Splice_Rec_1654590,Human_Splice_Rec_1654591,Human_Splice_Rec_1654594,Human_Splice_Rec_1654595,Human_Splice_Rec_1654600,Human_Splice_Rec_1654601,Human_Splice_Rec_1654608,Human_Splice_Rec_1654609,Human_Splice_Rec_1654618,Human_Splice_Rec_1654619,Human_Splice_Rec_1654624,Human_Splice_Rec_1654625,Human_Splice_Rec_1654632,Human_Splice_Rec_1654633,Human_Splice_Rec_1654640,Human_Splice_Rec_1654644 RMVar_hsa_circ_118232,RMVar_hsa_circ_116152,RMVar_hsa_circ_175389,RMVar_hsa_circ_175390 72506 RMVar_ID_72506 Human_SNP_ID_590621667 m1A Human chr16 + 635279 635279 635279 GAGCGGGAGGCCCGCCGTGGACAGGCCCACTCACCCCGTAGGTGATGAGCAGGGCCCTGGGTTTG GAGCGGGAGGCCCGCCGTGGACAGGCCCACTCTCCCCGTAGGTGATGAGCAGGGCCCTGGGTTTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:635276..635377;chr16:635276..635427 32194978 MeRIP-seq:(Medium) rs757347973 Functional Loss SNV dbSNP153 33..33 33 - - - 72507 RMVar_ID_72507 Human_SNP_ID_590621865 m1A Human chr16 + 635667 635667 635667 CATGGGCCATGTTGATGCAGAGCAACAGGTCCAGCGACTGTGGCAGGATCCCGCCCCAGTGCTCC CATGGGCCATGTTGATGCAGAGCAACAGGTCCCGCGACTGTGGCAGGATCCCGCCCCAGTGCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:635664..635788 26863196 MeRIP-seq:(Medium) rs1000286847 Functional Loss SNV dbSNP153 33..33 33 - - - 72508 RMVar_ID_72508 Human_SNP_ID_590621870 m1A Human chr16 + 635671 635671 635671 GGCCATGTTGATGCAGAGCAACAGGTCCAGCGACTGTGGCAGGATCCCGCCCCAGTGCTCCCAGC GGCCATGTTGATGCAGAGCAACAGGTCCAGCGTCTGTGGCAGGATCCCGCCCCAGTGCTCCCAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:635667..635812 26863196 MeRIP-seq:(Medium) rs1278217875 Functional Loss SNV dbSNP153 33..33 33 - - - 72509 RMVar_ID_72509 Human_SNP_ID_590622068 m1A Human chr16 + 636104 636104 636104 GTGGCCGCCCCGGGGGCCGCACCTGTCCAGGCAGCGCTGGTCCACGTCCGACGGCTGCCACTCGG GTGGCCGCCCCGGGGGCCGCACCTGTCCAGGCGGCGCTGGTCCACGTCCGACGGCTGCCACTCGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:636101..636300 26863196 MeRIP-seq:(Medium) rs1315436648 Functional Loss SNV dbSNP153 33..33 33 - - - 72510 RMVar_ID_72510 Human_SNP_ID_590622069 m1A Human chr16 + 636104 636104 636104 GTGGCCGCCCCGGGGGCCGCACCTGTCCAGGCAGCGCTGGTCCACGTCCGACGGCTGCCACTCGG GTGGCCGCCCCGGGGGCCGCACCTGTCCAGGCTGCGCTGGTCCACGTCCGACGGCTGCCACTCGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:636101..636300 26863196 MeRIP-seq:(Medium) rs1315436648 Functional Loss SNV dbSNP153 33..33 33 - - - 72511 RMVar_ID_72511 Human_SNP_ID_590622130 m1A Human chr16 + 636226 636226 636226 CGAGGACGCGGACGCCACGCTGGGCCGGATCCAGGTACTGCCGCAGCACGTGCAAGATGGGATCC CGAGGACGCGGACGCCACGCTGGGCCGGATCCGGGTACTGCCGCAGCACGTGCAAGATGGGATCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:636076..636325 26863196 MeRIP-seq:(Medium) rs1416744792 Functional Loss SNV dbSNP153 33..33 33 - - - 72512 RMVar_ID_72512 Human_SNP_ID_590622145 m1A Human chr16 - 636251 636251 636251 TGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACGTGCTGCGGCAGTACCTGGATCCG TGGCGGCGGCCGCGGAGCGGAACAAGGATCCCGTCTTGCACGTGCTGCGGCAGTACCTGGATCCG T C METTL26 Ensembl:ENSG00000130731 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:636150..636314 26863410 MeRIP-seq:(Medium) rs1293006592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478140,Human_RBP_ID_1520905,Human_RBP_ID_4393398,Human_RBP_ID_9324728,Human_RBP_ID_18682547,Human_RBP_ID_22441679,Human_RBP_ID_23696912 72513 RMVar_ID_72513 Human_SNP_ID_590622365 m1A Human chr16 - 636751 636751 636751 TGCAAGATTCCCATTCTTGCGACCCGGGTTCGATTCCCGGGCGGCGCACTTAGTTTTTTTTCCCA TGCAAGATTCCCATTCTTGCGACCCGGGTTCGGTTCCCGGGCGGCGCACTTAGTTTTTTTTCCCA T C TRG1,tRNA-Gly-CCC-2-2,TRG-CCC2-1 RNACentral:URS0000305D7E,RNACentral:URS0000502C74,RNACentral:URS0000868523 tRNA,tRNA,tRNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1001884005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269800,Human_RBP_ID_478143,Human_RBP_ID_1366231,Human_RBP_ID_1520906,Human_RBP_ID_5184345,Human_RBP_ID_5259747,Human_RBP_ID_5274846,Human_RBP_ID_5419538,Human_RBP_ID_5441061,Human_RBP_ID_5465364,Human_RBP_ID_5495985,Human_RBP_ID_6528551,Human_RBP_ID_8252256,Human_RBP_ID_8443864,Human_RBP_ID_9064302,Human_RBP_ID_12784852,Human_RBP_ID_17002666,Human_RBP_ID_17879666,Human_RBP_ID_18174158,Human_RBP_ID_18199938,Human_RBP_ID_18207480,Human_RBP_ID_18437983,Human_RBP_ID_18513058,Human_RBP_ID_18529842,Human_RBP_ID_18682548,Human_RBP_ID_19030965,Human_RBP_ID_22415823,Human_RBP_ID_23114142,Human_RBP_ID_23128516,Human_RBP_ID_23307924,Human_RBP_ID_23696913,Human_RBP_ID_24414757,Human_RBP_ID_24477466,Human_RBP_ID_26748851,Human_RBP_ID_27156126,Human_RBP_ID_27444496 72514 RMVar_ID_72514 Human_SNP_ID_590622366 m1A Human chr16 - 636751 636751 636751 TGCAAGATTCCCATTCTTGCGACCCGGGTTCGATTCCCGGGCGGCGCACTTAGTTTTTTTTCCCA TGCAAGATTCCCATTCTTGCGACCCGGGTTCGCTTCCCGGGCGGCGCACTTAGTTTTTTTTCCCA T G TRG1,tRNA-Gly-CCC-2-2,TRG-CCC2-1 RNACentral:URS0000305D7E,RNACentral:URS0000502C74,RNACentral:URS0000868523 tRNA,tRNA,tRNA exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1001884005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269800,Human_RBP_ID_478143,Human_RBP_ID_1366231,Human_RBP_ID_1520906,Human_RBP_ID_5184345,Human_RBP_ID_5259747,Human_RBP_ID_5274846,Human_RBP_ID_5419538,Human_RBP_ID_5441061,Human_RBP_ID_5465364,Human_RBP_ID_5495985,Human_RBP_ID_6528551,Human_RBP_ID_8252256,Human_RBP_ID_8443864,Human_RBP_ID_9064302,Human_RBP_ID_12784852,Human_RBP_ID_17002666,Human_RBP_ID_17879666,Human_RBP_ID_18174158,Human_RBP_ID_18199938,Human_RBP_ID_18207480,Human_RBP_ID_18437983,Human_RBP_ID_18513058,Human_RBP_ID_18529842,Human_RBP_ID_18682548,Human_RBP_ID_19030965,Human_RBP_ID_22415823,Human_RBP_ID_23114142,Human_RBP_ID_23128516,Human_RBP_ID_23307924,Human_RBP_ID_23696913,Human_RBP_ID_24414757,Human_RBP_ID_24477466,Human_RBP_ID_26748851,Human_RBP_ID_27156126,Human_RBP_ID_27444496 72515 RMVar_ID_72515 Human_SNP_ID_590624270 m1A Human chr16 - 641883 641883 641883 CGGGCGCCGCGGGGAGGGGGCGGGCCCGCTACACGCCCCCGGCCCTTAAAGGGCCCGCACGGGCT CGGGCGCCGCGGGGAGGGGGCGGGCCCGCTACCCGCCCCCGGCCCTTAAAGGGCCCGCACGGGCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:641879..642251 26863196 MeRIP-seq:(Medium) rs568000513 Functional Loss SNV dbSNP153 33..33 33 - - - 72516 RMVar_ID_72516 Human_SNP_ID_590624432 m1A Human chr16 + 642195 642195 642195 GAAATGCCGGCAGCCCGCGCCGCCGACCTCGCAGCCCCCGCGGGCGCAGCCCTTTGCGCAGCCGC GAAATGCCGGCAGCCCGCGCCGCCGACCTCGCGGCCCCCGCGGGCGCAGCCCTTTGCGCAGCCGC A G MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:641891..642817 32194978 MeRIP-seq:(Medium) rs1263733643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5237167,Human_RBP_ID_18982771 Human_Splice_Rec_1654664,Human_Splice_Rec_1654665,Human_Splice_Rec_1654672,Human_Splice_Rec_1654673,Human_Splice_Rec_1654682,Human_Splice_Rec_1654683,Human_Splice_Rec_1654686,Human_Splice_Rec_1654687 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72517 RMVar_ID_72517 Human_SNP_ID_590624704 m1A Human chr16 + 642949 642949 642949 CTCCCAGGCCTGTGGATTTTGCTGTGGCCCCAAGCCGGCCCGAAGGCTCCTGGAGGTGGTAGGGT CTCCCAGGCCTGTGGATTTTGCTGTGGCCCCACGCCGGCCCGAAGGCTCCTGGAGGTGGTAGGGT A C MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:642944..643072 26863196 MeRIP-seq:(Medium) rs1364832942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27244735 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72518 RMVar_ID_72518 Human_SNP_ID_590625550 m1A Human chr16 + 645620 645620 645620 GTGGGAGATGGATAGGGGAGGCAGTAAGATAAACTGAGGCGATATAAGTAATAAGATGAAACGGG GTGGGAGATGGATAGGGGAGGCAGTAAGATAAGCTGAGGCGATATAAGTAATAAGATGAAACGGG A G MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:645617..645812 26863196 MeRIP-seq:(Medium) rs1439052816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72519 RMVar_ID_72519 Human_SNP_ID_590625808 m1A Human chr16 + 646433 646408 646434 GGCCACCAGACCCTGCCAGCCCTGGGGCCGGCAGGACCCTGCGCCCCTCAAGACACTCCTCTTTA GGCCACCA__________________________GACCCTGCGCCCCTCAAGACACTCCTCTTTA AGACCCTGCCAGCCCTGGGGCCGGCAG A MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:646423..646600 26863196 MeRIP-seq:(Medium) rs1236642304 Functional Loss DEL dbSNP153 9..34 33 - - - Human_RBP_ID_22415260,Human_RBP_ID_22541014,Human_RBP_ID_26779934 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72520 RMVar_ID_72520 Human_SNP_ID_590625812 m1A Human chr16 + 646433 646417 646434 GGCCACCAGACCCTGCCAGCCCTGGGGCCGGCAGGACCCTGCGCCCCTCAAGACACTCCTCTTTA GGCCACCAGACCCTGCC_________________GACCCTGCGCCCCTCAAGACACTCCTCTTTA CAGCCCTGGGGCCGGCAG C MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:646423..646600 26863196 MeRIP-seq:(Medium) rs1158770919 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_22415260,Human_RBP_ID_22541014,Human_RBP_ID_26779934 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72521 RMVar_ID_72521 Human_SNP_ID_590626134 m1A Human chr16 + 647389 647389 647389 GCCAGGCAGCACCGCACCTGGGATGGGCACCAACCATGTCCGTCTCCTCCCTTCCTGCAGTCCAG GCCAGGCAGCACCGCACCTGGGATGGGCACCAGCCATGTCCGTCTCCTCCCTTCCTGCAGTCCAG A G MCRIP2 Ensembl:ENSG00000172366 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:647388..647567 26863196 MeRIP-seq:(Medium) rs748172854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8084439,Human_RBP_ID_18481678,Human_RBP_ID_21971765,Human_RBP_ID_22541015,Human_RBP_ID_22652714,Human_RBP_ID_22941331 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391 72522 RMVar_ID_72522 Human_SNP_ID_590626514 m1A Human chr16 + 648202 648202 648202 AGAATCACCAGCTGTTCCTAGTGGCTGCTGGGAGGGGGCGCTGCTACACGGCCGACCTGTCGCCA AGAATCACCAGCTGTTCCTAGTGGCTGCTGGGGGGGGGCGCTGCTACACGGCCGACCTGTCGCCA A G MCRIP2 Ensembl:ENSG00000172366 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:648151..648402;chr16:648157..648302 26863196 MeRIP-seq:(Medium) rs1408801351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478617,Human_RBP_ID_5113271,Human_RBP_ID_5236444,Human_RBP_ID_26809793 Human_Splice_Rec_1654660,Human_Splice_Rec_1654670,Human_Splice_Rec_1654680,Human_Splice_Rec_1654690,Human_Splice_Rec_1654698,Human_Splice_Rec_1654704,Human_Splice_Rec_1654708 Human_miRNA_ID_2650331,Human_miRNA_ID_2652283,Human_miRNA_ID_2756843 RMVar_hsa_circ_86271,RMVar_hsa_circ_175391,RMVar_hsa_circ_80146,RMVar_hsa_circ_175393 72523 RMVar_ID_72523 Human_SNP_ID_590627041 m1A Human chr16 - 649480 649480 649480 GGGGCCCTGAGCGCTCCGGCCGCCGACCCTGGACCCCGGAACCCCGGAACCCGGGATCCTCGGGA GGGGCCCTGAGCGCTCCGGCCGCCGACCCTGGCCCCCGGAACCCCGGAACCCGGGATCCTCGGGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:649430..649726;chr16:649430..649543 26863196 MeRIP-seq:(Medium) rs897429337 Functional Loss SNV dbSNP153 33..33 33 - - - 72524 RMVar_ID_72524 Human_SNP_ID_590628269 m1A Human chr16 + 652039 652039 652039 GAGGTGCCCGTGGCCCGCACCGGCTCCTGCGAAGTGAGTGCCCATCCCACAGCAGGCGGGGCCTG GAGGTGCCCGTGGCCCGCACCGGCTCCTGCGACGTGAGTGCCCATCCCACAGCAGGCGGGGCCTG A C WDR90 Ensembl:ENSG00000161996 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:651989..652271 32194978 MeRIP-seq:(Medium) rs566387037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19072637 Human_Splice_Rec_1654725,Human_Splice_Rec_1654775,Human_Splice_Rec_1654853,Human_Splice_Rec_1654885,Human_Splice_Rec_1654917 RMVar_hsa_circ_100909,RMVar_hsa_circ_175395 72525 RMVar_ID_72525 Human_SNP_ID_590629523 m1A Human chr16 - 655067 655064 655067 GTGTGCGCCTTTGCCAGAACGACCACCTCGCCACCGAGGCCCACCTGGCCGGTGCCCCAGGCCAC GTGTGCGCCTTTGCCAGAACGACCACCTCGCC___GAGGCCCACCTGGCCGGTGCCCCAGGCCAC CGGT C AL022341.2 Ensembl:ENSG00000262528 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:654752..655152 32194978 MeRIP-seq:(Medium) rs1567215955 Functional Loss DEL dbSNP153 33..35 33 - - - 72526 RMVar_ID_72526 Human_SNP_ID_590630278 m1A Human chr16 + 656341 656335 656342 GGGCCCCGTCAGCTCAGTCTGTGTCAGCCCCGATGGCCTCCGTGTGCTGTCTGCCACCTCCTCGG GGGCCCCGTCAGCTCAGTCTGTGTCAG_______GGCCTCCGTGTGCTGTCTGCCACCTCCTCGG GCCCCGAT G WDR90 Ensembl:ENSG00000161996 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:656295..656523 26863196 MeRIP-seq:(Medium) rs1362885029 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_26328017 Human_Splice_Rec_1654792,Human_Splice_Rec_1654934,Human_Splice_Rec_1654996 RMVar_hsa_circ_4552,RMVar_hsa_circ_100909,RMVar_hsa_circ_96149,RMVar_hsa_circ_175395,RMVar_hsa_circ_175396,RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 72527 RMVar_ID_72527 Human_SNP_ID_590630285 m1A Human chr16 + 656341 656341 656341 GGGCCCCGTCAGCTCAGTCTGTGTCAGCCCCGATGGCCTCCGTGTGCTGTCTGCCACCTCCTCGG GGGCCCCGTCAGCTCAGTCTGTGTCAGCCCCGCTGGCCTCCGTGTGCTGTCTGCCACCTCCTCGG A C WDR90 Ensembl:ENSG00000161996 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:656295..656523 26863196 MeRIP-seq:(Medium) rs1301906406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26328017 Human_Splice_Rec_1654792,Human_Splice_Rec_1654934,Human_Splice_Rec_1654996 RMVar_hsa_circ_4552,RMVar_hsa_circ_100909,RMVar_hsa_circ_96149,RMVar_hsa_circ_175395,RMVar_hsa_circ_175396,RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 72528 RMVar_ID_72528 Human_SNP_ID_590630488 m1A Human chr16 + 656739 656739 656739 CCTCAGCACGGCCCCTGTCCCACAGCTATACGACTTCACATCATCAGAGGACGCCCCGTGCGCTG CCTCAGCACGGCCCCTGTCCCACAGCTATACGTCTTCACATCATCAGAGGACGCCCCGTGCGCTG A T WDR90 Ensembl:ENSG00000161996 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:656726..656875 26863196 MeRIP-seq:(Medium) rs1202829757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45168 Human_Splice_Rec_1654740,Human_Splice_Rec_1654794,Human_Splice_Rec_1654936,Human_Splice_Rec_1654988,Human_Splice_Rec_1654998,Human_Splice_Rec_1655072,Human_Splice_Rec_1655112 RMVar_hsa_circ_4552,RMVar_hsa_circ_100909,RMVar_hsa_circ_96149,RMVar_hsa_circ_175395,RMVar_hsa_circ_175396,RMVar_hsa_circ_175399,RMVar_hsa_circ_92716,RMVar_hsa_circ_38656 72529 RMVar_ID_72529 Human_SNP_ID_590631277 m1A Human chr16 - 658322 658322 658322 TGAGGCTCACCTCCCGGATGATGCGGCCCGACACAGCATCCAGCACCACGACTCTGTTGGACGAG TGAGGCTCACCTCCCGGATGATGCGGCCCGACGCAGCATCCAGCACCACGACTCTGTTGGACGAG T C lnc-METTL26-6,lnc-METTL26-6:2 RNACentral:URS00008B5C2D,RNACentral:URS00009B1F30 lincRNA,lincRNA exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:656373..661193 32194978 MeRIP-seq:(Medium) rs773887230 Functional Loss SNV dbSNP153 33..33 33 - - - 72530 RMVar_ID_72530 Human_SNP_ID_590632569 m1A Human chr16 - 660995 660984 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG___________GAGGGGCCGAACAGGGGGCGGG CCCCAGGCCCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1567220524 Functional Loss DEL dbSNP153 33..43 33 - - - 72531 RMVar_ID_72531 Human_SNP_ID_590632571 m1A Human chr16 - 661025 660986 661025 AAGAAGCCTGTGCGCAGAGAGGGCGGGGCCTGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGG AAGAAGCCTGTGCGCAGAGAGGGCGGGGCCTG_________________________________ CCAGGCCCCTCCCCGCCCCCCCCCCCCCCCGGCCCGGCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1476791478 Functional Loss DEL dbSNP153 33..65 33 - - - 72532 RMVar_ID_72532 Human_SNP_ID_590632573 m1A Human chr16 - 660995 660986 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG_________GGGAGGGGCCGAACAGGGGGCGGG CCAGGCCCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1567220530 Functional Loss DEL dbSNP153 33..41 33 - - - 72533 RMVar_ID_72533 Human_SNP_ID_590632609 m1A Human chr16 - 660995 660991 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG____GCCTGGGGAGGGGCCGAACAGGGGGCGGG CCCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1567220591 Functional Loss DEL dbSNP153 33..36 33 - - - 72534 RMVar_ID_72534 Human_SNP_ID_590632613 m1A Human chr16 - 660995 660992 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG___GGCCTGGGGAGGGGCCGAACAGGGGGCGGG CCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1567220598 Functional Loss DEL dbSNP153 33..35 33 - - - 72535 RMVar_ID_72535 Human_SNP_ID_590632614 m1A Human chr16 - 660995 660993 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG__GGGCCTGGGGAGGGGCCGAACAGGGGGCGGG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1329067985 Functional Loss DEL dbSNP153 33..34 33 - - - 72536 RMVar_ID_72536 Human_SNP_ID_590632617 m1A Human chr16 - 660995 660994 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGG_GGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs1214790153 Functional Loss DEL dbSNP153 33..33 33 - - - 72537 RMVar_ID_72537 Human_SNP_ID_590632622 m1A Human chr16 - 660995 660995 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGGGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs200911762 Functional Loss SNV dbSNP153 33..33 33 - - - 72538 RMVar_ID_72538 Human_SNP_ID_590632623 m1A Human chr16 - 660995 660995 660995 TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG TGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGCGGGGCCTGGGGAGGGGCCGAACAGGGGGCGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs200911762 Functional Loss SNV dbSNP153 33..33 33 - - - 72539 RMVar_ID_72539 Human_SNP_ID_590632714 m1A Human chr16 - 661025 661025 661025 AAGAAGCCTGTGCGCAGAGAGGGCGGGGCCTGAGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGG AAGAAGCCTGTGCGCAGAGAGGGCGGGGCCTGGGGCCGGGCCGGGGGGGGGGGGGGGCGGGGAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:660976..661050 26863196 MeRIP-seq:(Medium) rs757118354 Functional Loss SNV dbSNP153 33..33 33 - - - 72540 RMVar_ID_72540 Human_SNP_ID_590633673 m1A Human chr16 + 662794 662794 662794 TGGGCACCACGGCGGGCACGCTGTGGTTTGTCAGCTGGGCCGAGGGCACCAGCACACGTCTCATC TGGGCACCACGGCGGGCACGCTGTGGTTTGTCGGCTGGGCCGAGGGCACCAGCACACGTCTCATC A G WDR90 Ensembl:ENSG00000161996 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:662745..662908 26863196 MeRIP-seq:(Medium) rs752546093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891027,Human_RBP_ID_18982809,Human_RBP_ID_22944931 Human_Splice_Rec_1654823,Human_Splice_Rec_1654965,Human_Splice_Rec_1655159,Human_Splice_Rec_1655183 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 72541 RMVar_ID_72541 Human_SNP_ID_590633868 m1A Human chr16 + 663174 663174 663174 AAGAAATCACATCAGTCCGGGCGTGGTGGTTCATGCCTGTGATCCCAGCACTCTGGGAGGCCAAG AAGAAATCACATCAGTCCGGGCGTGGTGGTTCGTGCCTGTGATCCCAGCACTCTGGGAGGCCAAG A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs536992544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1522045,Human_RBP_ID_12800819 Human_Splice_Rec_1655184 Human_miRNA_ID_2775293,Human_miRNA_ID_2778071 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 72542 RMVar_ID_72542 Human_SNP_ID_590634160 m1A Human chr16 - 664104 664104 664104 ACACGGAGCTTGTGCTGTGACGACTACACCTCAGCAAACCTGCTTCCAGAAAAGTAAACAACCCT ACACGGAGCTTGTGCTGTGACGACTACACCTCGGCAAACCTGCTTCCAGAAAAGTAAACAACCCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:664101..664328 26863196 MeRIP-seq:(Medium) rs1057363791 Functional Loss SNV dbSNP153 33..33 33 - - - 72543 RMVar_ID_72543 Human_SNP_ID_590634291 m1A Human chr16 + 664431 664431 664431 GGCCAAATACTGTTCCATTGTACGGATAGATCATGTGTGTGTCCATCCACCAGGGCTGGGAAATT GGCCAAATACTGTTCCATTGTACGGATAGATCGTGTGTGTGTCCATCCACCAGGGCTGGGAAATT A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:664401..664550 26863196 MeRIP-seq:(Medium) rs1398531241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1088857,Human_RBP_ID_1522074,Human_RBP_ID_1845958,Human_RBP_ID_4392714,Human_RBP_ID_12800979,Human_RBP_ID_18683636,Human_RBP_ID_22941738,Human_RBP_ID_26948583 72544 RMVar_ID_72544 Human_SNP_ID_590634297 m1A Human chr16 + 664443 664443 664443 TTCCATTGTACGGATAGATCATGTGTGTGTCCATCCACCAGGGCTGGGAAATTCGGGTCCTGAGA TTCCATTGTACGGATAGATCATGTGTGTGTCCGTCCACCAGGGCTGGGAAATTCGGGTCCTGAGA A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:664432..664529 26863196 MeRIP-seq:(Medium) rs911897192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1522074,Human_RBP_ID_4392714,Human_RBP_ID_12800979,Human_RBP_ID_18683638 72545 RMVar_ID_72545 Human_SNP_ID_590635976 m1A Human chr16 + 668210 668210 668210 GGAGCGGCTCCGGGCGGCAGCTATGAGGCGGGACGTGCGCATCCTGTTACTGGGCGAGGGTAGGC GGAGCGGCTCCGGGCGGCAGCTATGAGGCGGGGCGTGCGCATCCTGTTACTGGGCGAGGGTAGGC A G RHOT2 Ensembl:ENSG00000140983 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr16:668127..668321;chr16:668125..668217 26863410 MeRIP-seq:(Medium) rs761643701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234906,Human_RBP_ID_479047,Human_RBP_ID_888192,Human_RBP_ID_3946884,Human_RBP_ID_4393403,Human_RBP_ID_5317189,Human_RBP_ID_5465789,Human_RBP_ID_18418859,Human_RBP_ID_18982818,Human_RBP_ID_22944357,Human_RBP_ID_23209499,Human_RBP_ID_26328354,Human_RBP_ID_27837663 Human_Splice_Rec_1655251,Human_Splice_Rec_1655267,Human_Splice_Rec_1655283,Human_Splice_Rec_1655295,Human_Splice_Rec_1655307,Human_Splice_Rec_1655343,Human_Splice_Rec_1655377,Human_Splice_Rec_1655393,Human_Splice_Rec_1655415,Human_Splice_Rec_1655431,Human_Splice_Rec_1655451,Human_Splice_Rec_1655477,Human_Splice_Rec_1655499,Human_Splice_Rec_1655511,Human_Splice_Rec_1655535 72546 RMVar_ID_72546 Human_SNP_ID_590636715 m1A Human chr16 + 669555 669555 669555 GTCACCCACACCTCATCACTGTTCCCTCAGGCAAACGTGGTGTGTGTGGTGTATGACGTCTCTGA GTCACCCACACCTCATCACTGTTCCCTCAGGCCAACGTGGTGTGTGTGGTGTATGACGTCTCTGA A C RHOT2 Ensembl:ENSG00000140983 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:669551..669625 26863196 MeRIP-seq:(Medium) rs781451058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761465,Human_RBP_ID_2481875,Human_RBP_ID_3946891,Human_RBP_ID_18982826,Human_RBP_ID_22738772,Human_RBP_ID_26328360,Human_RBP_ID_26948735 Human_Splice_Rec_1655244,Human_Splice_Rec_1655245,Human_Splice_Rec_1655258,Human_Splice_Rec_1655259,Human_Splice_Rec_1655274,Human_Splice_Rec_1655275,Human_Splice_Rec_1655288,Human_Splice_Rec_1655289,Human_Splice_Rec_1655314,Human_Splice_Rec_1655315,Human_Splice_Rec_1655348,Human_Splice_Rec_1655349,Human_Splice_Rec_1655384,Human_Splice_Rec_1655385,Human_Splice_Rec_1655398,Human_Splice_Rec_1655399,Human_Splice_Rec_1655458,Human_Splice_Rec_1655459,Human_Splice_Rec_1655506,Human_Splice_Rec_1655507,Human_Splice_Rec_1655518,Human_Splice_Rec_1655519,Human_Splice_Rec_1655564,Human_Splice_Rec_1655565,Human_Splice_Rec_1655580 RMVar_hsa_circ_104960,RMVar_hsa_circ_97018,RMVar_hsa_circ_119501,RMVar_hsa_circ_175402,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72547 RMVar_ID_72547 Human_SNP_ID_590637027 m1A Human chr16 + 670096 670096 670096 CAGCTGGGAGCCATGTGCCCGCGGGCAGCCTCACTTCACAGCCAGGCTTTGCTTTTCAGATTCGA CAGCTGGGAGCCATGTGCCCGCGGGCAGCCTCGCTTCACAGCCAGGCTTTGCTTTTCAGATTCGA A G RHOT2 Ensembl:ENSG00000140983 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:670092..670375 26863196 MeRIP-seq:(Medium) rs569759155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260933,Human_RBP_ID_761467,Human_RBP_ID_1522252,Human_RBP_ID_22541036,Human_RBP_ID_22652720,Human_RBP_ID_27837671 Human_Splice_Rec_1655247,Human_Splice_Rec_1655261,Human_Splice_Rec_1655277,Human_Splice_Rec_1655291,Human_Splice_Rec_1655299,Human_Splice_Rec_1655317,Human_Splice_Rec_1655351,Human_Splice_Rec_1655387,Human_Splice_Rec_1655401,Human_Splice_Rec_1655421,Human_Splice_Rec_1655439,Human_Splice_Rec_1655461,Human_Splice_Rec_1655481,Human_Splice_Rec_1655521,Human_Splice_Rec_1655543,Human_Splice_Rec_1655557,Human_Splice_Rec_1655567,Human_Splice_Rec_1655581 RMVar_hsa_circ_104960,RMVar_hsa_circ_97018,RMVar_hsa_circ_119501,RMVar_hsa_circ_175402,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72548 RMVar_ID_72548 Human_SNP_ID_590637028 m1A Human chr16 + 670096 670096 670096 CAGCTGGGAGCCATGTGCCCGCGGGCAGCCTCACTTCACAGCCAGGCTTTGCTTTTCAGATTCGA CAGCTGGGAGCCATGTGCCCGCGGGCAGCCTCTCTTCACAGCCAGGCTTTGCTTTTCAGATTCGA A T RHOT2 Ensembl:ENSG00000140983 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:670092..670375 26863196 MeRIP-seq:(Medium) rs569759155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260933,Human_RBP_ID_761467,Human_RBP_ID_1522252,Human_RBP_ID_22541036,Human_RBP_ID_22652720,Human_RBP_ID_27837671 Human_Splice_Rec_1655247,Human_Splice_Rec_1655261,Human_Splice_Rec_1655277,Human_Splice_Rec_1655291,Human_Splice_Rec_1655299,Human_Splice_Rec_1655317,Human_Splice_Rec_1655351,Human_Splice_Rec_1655387,Human_Splice_Rec_1655401,Human_Splice_Rec_1655421,Human_Splice_Rec_1655439,Human_Splice_Rec_1655461,Human_Splice_Rec_1655481,Human_Splice_Rec_1655521,Human_Splice_Rec_1655543,Human_Splice_Rec_1655557,Human_Splice_Rec_1655567,Human_Splice_Rec_1655581 RMVar_hsa_circ_104960,RMVar_hsa_circ_97018,RMVar_hsa_circ_119501,RMVar_hsa_circ_175402,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72549 RMVar_ID_72549 Human_SNP_ID_590637031 m1A Human chr16 + 670103 670103 670103 GAGCCATGTGCCCGCGGGCAGCCTCACTTCACAGCCAGGCTTTGCTTTTCAGATTCGAACTAAGT GAGCCATGTGCCCGCGGGCAGCCTCACTTCACGGCCAGGCTTTGCTTTTCAGATTCGAACTAAGT A G RHOT2 Ensembl:ENSG00000140983 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:670101..670150 26863196 MeRIP-seq:(Medium) rs377316300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761467,Human_RBP_ID_1522252,Human_RBP_ID_18683819,Human_RBP_ID_22541036,Human_RBP_ID_22652720,Human_RBP_ID_25227419 Human_Splice_Rec_1655247,Human_Splice_Rec_1655261,Human_Splice_Rec_1655277,Human_Splice_Rec_1655291,Human_Splice_Rec_1655299,Human_Splice_Rec_1655317,Human_Splice_Rec_1655351,Human_Splice_Rec_1655387,Human_Splice_Rec_1655401,Human_Splice_Rec_1655421,Human_Splice_Rec_1655439,Human_Splice_Rec_1655461,Human_Splice_Rec_1655481,Human_Splice_Rec_1655521,Human_Splice_Rec_1655543,Human_Splice_Rec_1655557,Human_Splice_Rec_1655567,Human_Splice_Rec_1655581 RMVar_hsa_circ_104960,RMVar_hsa_circ_97018,RMVar_hsa_circ_119501,RMVar_hsa_circ_175402,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72550 RMVar_ID_72550 Human_SNP_ID_590637126 m1A Human chr16 + 670275 670275 670275 ACCCAGGGTGCCCATCATCCTAGTGGGCAACAAGTCAGACCTGCGGTCGGGGAGCTCCATGGAGG ACCCAGGGTGCCCATCATCCTAGTGGGCAACACGTCAGACCTGCGGTCGGGGAGCTCCATGGAGG A C RHOT2 Ensembl:ENSG00000140983 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:670101..670805 26863196 MeRIP-seq:(Medium) rs748110084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889231,Human_RBP_ID_3946898,Human_RBP_ID_9373539,Human_RBP_ID_18982829,Human_RBP_ID_22802242,Human_RBP_ID_27811415 Human_Splice_Rec_1655248,Human_Splice_Rec_1655249,Human_Splice_Rec_1655262,Human_Splice_Rec_1655263,Human_Splice_Rec_1655278,Human_Splice_Rec_1655279,Human_Splice_Rec_1655292,Human_Splice_Rec_1655293,Human_Splice_Rec_1655300,Human_Splice_Rec_1655301,Human_Splice_Rec_1655318,Human_Splice_Rec_1655319,Human_Splice_Rec_1655352,Human_Splice_Rec_1655353,Human_Splice_Rec_1655388,Human_Splice_Rec_1655389,Human_Splice_Rec_1655402,Human_Splice_Rec_1655403,Human_Splice_Rec_1655422,Human_Splice_Rec_1655423,Human_Splice_Rec_1655440,Human_Splice_Rec_1655441,Human_Splice_Rec_1655462,Human_Splice_Rec_1655463,Human_Splice_Rec_1655482,Human_Splice_Rec_1655483,Human_Splice_Rec_1655509,Human_Splice_Rec_1655522,Human_Splice_Rec_1655523,Human_Splice_Rec_1655544,Human_Splice_Rec_1655545,Human_Splice_Rec_1655558,Human_Splice_Rec_1655559,Human_Splice_Rec_1655568,Human_Splice_Rec_1655569,Human_Splice_Rec_1655582,Human_Splice_Rec_1655583 RMVar_hsa_circ_104960,RMVar_hsa_circ_119501,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72551 RMVar_ID_72551 Human_SNP_ID_590637127 m1A Human chr16 + 670275 670275 670275 ACCCAGGGTGCCCATCATCCTAGTGGGCAACAAGTCAGACCTGCGGTCGGGGAGCTCCATGGAGG ACCCAGGGTGCCCATCATCCTAGTGGGCAACAGGTCAGACCTGCGGTCGGGGAGCTCCATGGAGG A G RHOT2 Ensembl:ENSG00000140983 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:670101..670805 26863196 MeRIP-seq:(Medium) rs748110084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889231,Human_RBP_ID_3946898,Human_RBP_ID_9373539,Human_RBP_ID_18982829,Human_RBP_ID_22802242,Human_RBP_ID_27811415 Human_Splice_Rec_1655248,Human_Splice_Rec_1655249,Human_Splice_Rec_1655262,Human_Splice_Rec_1655263,Human_Splice_Rec_1655278,Human_Splice_Rec_1655279,Human_Splice_Rec_1655292,Human_Splice_Rec_1655293,Human_Splice_Rec_1655300,Human_Splice_Rec_1655301,Human_Splice_Rec_1655318,Human_Splice_Rec_1655319,Human_Splice_Rec_1655352,Human_Splice_Rec_1655353,Human_Splice_Rec_1655388,Human_Splice_Rec_1655389,Human_Splice_Rec_1655402,Human_Splice_Rec_1655403,Human_Splice_Rec_1655422,Human_Splice_Rec_1655423,Human_Splice_Rec_1655440,Human_Splice_Rec_1655441,Human_Splice_Rec_1655462,Human_Splice_Rec_1655463,Human_Splice_Rec_1655482,Human_Splice_Rec_1655483,Human_Splice_Rec_1655509,Human_Splice_Rec_1655522,Human_Splice_Rec_1655523,Human_Splice_Rec_1655544,Human_Splice_Rec_1655545,Human_Splice_Rec_1655558,Human_Splice_Rec_1655559,Human_Splice_Rec_1655568,Human_Splice_Rec_1655569,Human_Splice_Rec_1655582,Human_Splice_Rec_1655583 RMVar_hsa_circ_104960,RMVar_hsa_circ_119501,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72552 RMVar_ID_72552 Human_SNP_ID_590637139 m1A Human chr16 - 670298 670298 670298 CTGGCTCATGATGGGGAGCACGGCCTCCATGGAGCTCCCCGACCGCAGGTCTGACTTGTTGCCCA CTGGCTCATGATGGGGAGCACGGCCTCCATGGGGCTCCCCGACCGCAGGTCTGACTTGTTGCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr16:670249..670332;chr16:670174..670521 26863196,32194978 MeRIP-seq:(Medium) rs1281112550 Functional Loss SNV dbSNP153 33..33 33 - - - 72553 RMVar_ID_72553 Human_SNP_ID_590637268 m1A Human chr16 + 670485 670485 670485 CAGTGTTCGGCCAAGAACCTGAGGAACATCTCAGAGCTGTTCTACTACGCCCAGAAGGCCGTCCT CAGTGTTCGGCCAAGAACCTGAGGAACATCTCGGAGCTGTTCTACTACGCCCAGAAGGCCGTCCT A G RHOT2 Ensembl:ENSG00000140983 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:670451..670550 26863196 MeRIP-seq:(Medium) rs761357531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1846170,Human_RBP_ID_3946901,Human_RBP_ID_9372009,Human_RBP_ID_18683825,Human_RBP_ID_18982831,Human_RBP_ID_22802244,Human_RBP_ID_22946301,Human_RBP_ID_23114011,Human_RBP_ID_24558628,Human_RBP_ID_26328363,Human_RBP_ID_26948785,Human_RBP_ID_27811417 Human_Splice_Rec_1655250,Human_Splice_Rec_1655264,Human_Splice_Rec_1655265,Human_Splice_Rec_1655280,Human_Splice_Rec_1655281,Human_Splice_Rec_1655294,Human_Splice_Rec_1655302,Human_Splice_Rec_1655320,Human_Splice_Rec_1655321,Human_Splice_Rec_1655354,Human_Splice_Rec_1655355,Human_Splice_Rec_1655390,Human_Splice_Rec_1655391,Human_Splice_Rec_1655404,Human_Splice_Rec_1655405,Human_Splice_Rec_1655424,Human_Splice_Rec_1655425,Human_Splice_Rec_1655442,Human_Splice_Rec_1655443,Human_Splice_Rec_1655464,Human_Splice_Rec_1655465,Human_Splice_Rec_1655484,Human_Splice_Rec_1655485,Human_Splice_Rec_1655510,Human_Splice_Rec_1655524,Human_Splice_Rec_1655525,Human_Splice_Rec_1655546,Human_Splice_Rec_1655547,Human_Splice_Rec_1655560,Human_Splice_Rec_1655561,Human_Splice_Rec_1655570,Human_Splice_Rec_1655571,Human_Splice_Rec_1655584,Human_Splice_Rec_1655585,Human_Splice_Rec_1655599,Human_Splice_Rec_1655617 RMVar_hsa_circ_104960,RMVar_hsa_circ_119501,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 72554 RMVar_ID_72554 Human_SNP_ID_590637566 m1A Human chr16 - 670947 670944 670947 CCCGCACGCCGCCCGCCACGTTCCTGCACACCACCGTCTTCACGTCCTCCAGGGCCTGCGGGGCC CCCGCACGCCGCCCGCCACGTTCCTGCACACC___GTCTTCACGTCCTCCAGGGCCTGCGGGGCC CGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:670751..671223;chr16:670780..671225 26863196 MeRIP-seq:(Medium) rs1158058208 Functional Loss DEL dbSNP153 33..35 33 - - - 72555 RMVar_ID_72555 Human_SNP_ID_590637731 m1A Human chr16 - 671168 671168 671168 GGGGAGAGATAGTCCGCAGTCAGCTCCAGGGCATCGCTGTAGCCGAAGCGCCGCAGGATGGTCCA GGGGAGAGATAGTCCGCAGTCAGCTCCAGGGCGTCGCTGTAGCCGAAGCGCCGCAGGATGGTCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:670736..671235 32194978 MeRIP-seq:(Medium) rs141691318 Functional Loss SNV dbSNP153 33..33 33 - - - 72556 RMVar_ID_72556 Human_SNP_ID_590637747 m1A Human chr16 + 671188 671188 671188 CGGCTACAGCGATGCCCTGGAGCTGACTGCGGACTATCTCTCCCCTCTGTGAGTGATGCCGGGGC CGGCTACAGCGATGCCCTGGAGCTGACTGCGGCCTATCTCTCCCCTCTGTGAGTGATGCCGGGGC A C RHOT2 Ensembl:ENSG00000140983 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:670857..671225 26863196 MeRIP-seq:(Medium) rs1450666186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818050,Human_RBP_ID_1522270,Human_RBP_ID_1846174,Human_RBP_ID_9373547,Human_RBP_ID_12804521,Human_RBP_ID_18982833 Human_Splice_Rec_1655327,Human_Splice_Rec_1655361,Human_Splice_Rec_1655411,Human_Splice_Rec_1655447,Human_Splice_Rec_1655469,Human_Splice_Rec_1655489,Human_Splice_Rec_1655530,Human_Splice_Rec_1655531,Human_Splice_Rec_1655577,Human_Splice_Rec_1655589,Human_Splice_Rec_1655604,Human_Splice_Rec_1655605,Human_Splice_Rec_1655621 Human_miRNA_ID_2137186,Human_miRNA_ID_2609822,Human_miRNA_ID_2665974 RMVar_hsa_circ_104960,RMVar_hsa_circ_125130,RMVar_hsa_circ_127472,RMVar_hsa_circ_175405,RMVar_hsa_circ_175406,RMVar_hsa_circ_175408,RMVar_hsa_circ_123926,RMVar_hsa_circ_175407 72557 RMVar_ID_72557 Human_SNP_ID_590638055 m1A Human chr16 + 671774 671774 671774 CTACCAGTTTGTGCAGAGAGTGTTTGAGAAGCACGACCAGGTGAGAGCATGGCGAGTCCCCTGCC CTACCAGTTTGTGCAGAGAGTGTTTGAGAAGCGCGACCAGGTGAGAGCATGGCGAGTCCCCTGCC A G RHOT2 Ensembl:ENSG00000140983 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:671671..672159 26863196 MeRIP-seq:(Medium) rs766993284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3946907,Human_RBP_ID_9373548,Human_RBP_ID_18162834,Human_RBP_ID_18984859 Human_Splice_Rec_1655328,Human_Splice_Rec_1655329,Human_Splice_Rec_1655362,Human_Splice_Rec_1655363,Human_Splice_Rec_1655412,Human_Splice_Rec_1655413,Human_Splice_Rec_1655448,Human_Splice_Rec_1655449,Human_Splice_Rec_1655470,Human_Splice_Rec_1655471,Human_Splice_Rec_1655490,Human_Splice_Rec_1655491,Human_Splice_Rec_1655532,Human_Splice_Rec_1655533,Human_Splice_Rec_1655578,Human_Splice_Rec_1655590,Human_Splice_Rec_1655591,Human_Splice_Rec_1655606,Human_Splice_Rec_1655607,Human_Splice_Rec_1655622,Human_Splice_Rec_1655623 RMVar_hsa_circ_104960,RMVar_hsa_circ_125130,RMVar_hsa_circ_127472,RMVar_hsa_circ_175405,RMVar_hsa_circ_175406,RMVar_hsa_circ_175408,RMVar_hsa_circ_123926,RMVar_hsa_circ_175407 72558 RMVar_ID_72558 Human_SNP_ID_590638208 m1A Human chr16 + 671960 671960 671960 GGGCCCCGAGCTCCCACGCACAGTCCGCACAGAGGCCGGCCGGTTGCCCCTGCACGGATACCTCT GGGCCCCGAGCTCCCACGCACAGTCCGCACAGCGGCCGGCCGGTTGCCCCTGCACGGATACCTCT A C RHOT2 Ensembl:ENSG00000140983 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:671912..672090 26863196 MeRIP-seq:(Medium) rs1447901480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3946908,Human_RBP_ID_26328369 Human_Splice_Rec_1655331,Human_Splice_Rec_1655365,Human_Splice_Rec_1655473,Human_Splice_Rec_1655493,Human_Splice_Rec_1655609,Human_Splice_Rec_1655625,Human_Splice_Rec_1655633 RMVar_hsa_circ_104960,RMVar_hsa_circ_127472,RMVar_hsa_circ_175406,RMVar_hsa_circ_175409,RMVar_hsa_circ_175408,RMVar_hsa_circ_123926,RMVar_hsa_circ_175407,RMVar_hsa_circ_338970 72559 RMVar_ID_72559 Human_SNP_ID_590639114 m1A Human chr16 - 673554 673545 673554 CCCTGTAGAGTGAGAAGCTGAGGACTGCGGCCACGGCGGCCCCGACAACCCCCAGCAGCCCCCGG CCCTGTAGAGTGAGAAGCTGAGGACTGCGGCC_________CCGACAACCCCCAGCAGCCCCCGG GGGCCGCCGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:673544..673688 26863196 MeRIP-seq:(Medium) rs779627353 Functional Loss DEL dbSNP153 33..41 33 - - - 72560 RMVar_ID_72560 Human_SNP_ID_590639129 m1A Human chr16 + 673576 673576 673576 GGGGCCGCCGTGGCCGCAGTCCTCAGCTTCTCACTCTACAGGGTCCTGGTGAAGAGCCAGTGAGG GGGGCCGCCGTGGCCGCAGTCCTCAGCTTCTCTCTCTACAGGGTCCTGGTGAAGAGCCAGTGAGG A T RHOT2 Ensembl:ENSG00000140983 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:673526..674124 32194978 MeRIP-seq:(Medium) rs199849249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1846212,Human_RBP_ID_5113777,Human_RBP_ID_8438461,Human_RBP_ID_18683932,Human_RBP_ID_22941869,Human_RBP_ID_27245637 Human_Splice_Rec_1655342,Human_Splice_Rec_1655376,Human_Splice_Rec_1655598,Human_Splice_Rec_1655642,Human_Splice_Rec_1655646,Human_Splice_Rec_1655648 72561 RMVar_ID_72561 Human_SNP_ID_590639206 m1A Human chr16 + 673751 673751 673751 GCGCCGGGACTTTTTGTTTCTGAAGGCAGTCGATCTGCAGCGGGGCCTTATGCTGCCATGCACTG GCGCCGGGACTTTTTGTTTCTGAAGGCAGTCGGTCTGCAGCGGGGCCTTATGCTGCCATGCACTG A G RHOT2 Ensembl:ENSG00000140983 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:673651..673881 26863410 MeRIP-seq:(Medium) rs1440361071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889234,Human_RBP_ID_1179028,Human_RBP_ID_1522327,Human_RBP_ID_3946918,Human_RBP_ID_5114072,Human_RBP_ID_5317193,Human_RBP_ID_5357190,Human_RBP_ID_9324733,Human_RBP_ID_12804846,Human_RBP_ID_18161900,Human_RBP_ID_18411320,Human_RBP_ID_18683937,Human_RBP_ID_18982842,Human_RBP_ID_22738773,Human_RBP_ID_23209207,Human_RBP_ID_26328373 72562 RMVar_ID_72562 Human_SNP_ID_590642117 m1A Human chr16 + 680480 680480 680480 TGCGGGGCTCCGGCTGCGGGCGCTGGGCCGCGAGGCGCGGAGCTTGGGAGCGGAGCCCAGGCCGT TGCGGGGCTCCGGCTGCGGGCGCTGGGCCGCGGGGCGCGGAGCTTGGGAGCGGAGCCCAGGCCGT A G STUB1 Ensembl:ENSG00000103266 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:680426..680569 26863410 MeRIP-seq:(Medium) rs1260691388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1522501,Human_RBP_ID_4383093,Human_RBP_ID_8941314,Human_RBP_ID_9324737,Human_RBP_ID_9353152,Human_RBP_ID_17121321,Human_RBP_ID_18418861,Human_RBP_ID_18684186 72563 RMVar_ID_72563 Human_SNP_ID_590642731 m1A Human chr16 + 681843 681843 681843 GCGAAACCACGAGGGTGATGAGGACGACAGCCACGTCCGGGCCCAGCAGGCCTGCATTGAGGCCA GCGAAACCACGAGGGTGATGAGGACGACAGCCGCGTCCGGGCCCAGCAGGCCTGCATTGAGGCCA A G STUB1 Ensembl:ENSG00000103266 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:681776..682035 26863196 MeRIP-seq:(Medium) rs538288405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005479,Human_RBP_ID_4383163,Human_RBP_ID_26328379 Human_Splice_Rec_1655708,Human_Splice_Rec_1655709,Human_Splice_Rec_1655720,Human_Splice_Rec_1655721,Human_Splice_Rec_1655730,Human_Splice_Rec_1655740,Human_Splice_Rec_1655741,Human_Splice_Rec_1655750,Human_Splice_Rec_1655756,Human_Splice_Rec_1655757,Human_Splice_Rec_1655766,Human_Splice_Rec_1655767,Human_Splice_Rec_1655774,Human_Splice_Rec_1655775,Human_Splice_Rec_1655780,Human_Splice_Rec_1655781 Human_miRNA_ID_1157614 72564 RMVar_ID_72564 Human_SNP_ID_590643138 m1A Human chr16 - 682497 682497 682497 GGGCTCCCCTGGACCAGGACGCCAGGTAGGGCAGGGAACCTCAGTAGTCCTCCACCCAGCCATTC GGGCTCCCCTGGACCAGGACGCCAGGTAGGGCGGGGAACCTCAGTAGTCCTCCACCCAGCCATTC T C JMJD8 Ensembl:ENSG00000161999 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:682446..682576 26863196 MeRIP-seq:(Medium) rs1433183550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445586 Human_miRNA_ID_461171,Human_miRNA_ID_927089,Human_miRNA_ID_2959259 RMVar_hsa_circ_123811,RMVar_hsa_circ_125274,RMVar_hsa_circ_175416,RMVar_hsa_circ_87665,RMVar_hsa_circ_93975,RMVar_hsa_circ_76366,RMVar_hsa_circ_175417,RMVar_hsa_circ_175414,RMVar_hsa_circ_175415,RMVar_hsa_circ_175413 72565 RMVar_ID_72565 Human_SNP_ID_590643577 m1A Human chr16 - 683177 683177 683177 CTGGCATGGACCCGGGTACTCAGAAGTGATCTACGGTCGTAAGGTCAGCACGGGGTGGGGGTTGA CTGGCATGGACCCGGGTACTCAGAAGTGATCTGCGGTCGTAAGGTCAGCACGGGGTGGGGGTTGA T C JMJD8 Ensembl:ENSG00000161999 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:683167..683404 32194978 MeRIP-seq:(Medium) rs1196550227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1522539,Human_RBP_ID_5356263 Human_Splice_Rec_1655800,Human_Splice_Rec_1655801,Human_Splice_Rec_1655814,Human_Splice_Rec_1655815,Human_Splice_Rec_1655826,Human_Splice_Rec_1655827,Human_Splice_Rec_1655838,Human_Splice_Rec_1655839,Human_Splice_Rec_1655852,Human_Splice_Rec_1655853,Human_Splice_Rec_1655866,Human_Splice_Rec_1655867,Human_Splice_Rec_1655878,Human_Splice_Rec_1655879,Human_Splice_Rec_1655884,Human_Splice_Rec_1655885,Human_Splice_Rec_1655894,Human_Splice_Rec_1655895,Human_Splice_Rec_1655910,Human_Splice_Rec_1655911,Human_Splice_Rec_1655916,Human_Splice_Rec_1655917,Human_Splice_Rec_1655930 RMVar_hsa_circ_123811,RMVar_hsa_circ_175416,RMVar_hsa_circ_93975,RMVar_hsa_circ_76366,RMVar_hsa_circ_175417,RMVar_hsa_circ_175415,RMVar_hsa_circ_101812,RMVar_hsa_circ_118528,RMVar_hsa_circ_175422,RMVar_hsa_circ_68065,RMVar_hsa_circ_175423,RMVar_hsa_circ_82658,RMVar_hsa_circ_86376,RMVar_hsa_circ_175425,RMVar_hsa_circ_25461,RMVar_hsa_circ_175424 72566 RMVar_ID_72566 Human_SNP_ID_590644046 m1A Human chr16 - 683781 683781 683781 CCGGCCACTAAGTCCCCTCCCCGCCCCCGCAGAGGTTCCGGGCCCTGTGCTCCCGCGACAGGTTG CCGGCCACTAAGTCCCCTCCCCGCCCCCGCAGGGGTTCCGGGCCCTGTGCTCCCGCGACAGGTTG T C JMJD8 Ensembl:ENSG00000161999 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:683763..683848 26863196 MeRIP-seq:(Medium) rs1469082513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22651314 Human_Splice_Rec_1655794,Human_Splice_Rec_1655795,Human_Splice_Rec_1655808,Human_Splice_Rec_1655809,Human_Splice_Rec_1655821,Human_Splice_Rec_1655834,Human_Splice_Rec_1655835,Human_Splice_Rec_1655848,Human_Splice_Rec_1655849,Human_Splice_Rec_1655860,Human_Splice_Rec_1655861,Human_Splice_Rec_1655872,Human_Splice_Rec_1655873,Human_Splice_Rec_1655889,Human_Splice_Rec_1655904,Human_Splice_Rec_1655905,Human_Splice_Rec_1655924,Human_Splice_Rec_1655925,Human_Splice_Rec_1655932,Human_Splice_Rec_1655933,Human_Splice_Rec_1655939 RMVar_hsa_circ_2671,RMVar_hsa_circ_123811,RMVar_hsa_circ_175417,RMVar_hsa_circ_118528,RMVar_hsa_circ_175423,RMVar_hsa_circ_86376,RMVar_hsa_circ_175425,RMVar_hsa_circ_96916,RMVar_hsa_circ_373490,RMVar_hsa_circ_175427,RMVar_hsa_circ_175428 72567 RMVar_ID_72567 Human_SNP_ID_590644156 m1A Human chr16 - 683911 683911 683911 TCCGGCCTGGCCGCGACTCTGCCCTTCTTTCCAGGTACGCCTTCGTCAGGCCCGTCATCCTGCAG TCCGGCCTGGCCGCGACTCTGCCCTTCTTTCCGGGTACGCCTTCGTCAGGCCCGTCATCCTGCAG T C JMJD8 Ensembl:ENSG00000161999 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:683796..683950 26863196 MeRIP-seq:(Medium) rs759401483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277699,Human_RBP_ID_4383270,Human_RBP_ID_18438104 Human_Splice_Rec_1655793,Human_Splice_Rec_1655807,Human_Splice_Rec_1655833,Human_Splice_Rec_1655847,Human_Splice_Rec_1655859,Human_Splice_Rec_1655871,Human_Splice_Rec_1655903,Human_Splice_Rec_1655923,Human_Splice_Rec_1655931 RMVar_hsa_circ_123811,RMVar_hsa_circ_175417,RMVar_hsa_circ_86376,RMVar_hsa_circ_175425 72568 RMVar_ID_72568 Human_SNP_ID_590644325 m1A Human chr16 - 684112 684112 684112 GGCCGGGGGCCGTGGCGGAGGAGGAGCGCTGCACGGTGGAGCGTCGGGCCGACCTCACCTACGCG GGCCGGGGGCCGTGGCGGAGGAGGAGCGCTGCGCGGTGGAGCGTCGGGCCGACCTCACCTACGCG T C JMJD8 Ensembl:ENSG00000161999 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:684101..684325 26863196 MeRIP-seq:(Medium) rs745348274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761706,Human_RBP_ID_891053,Human_RBP_ID_5316420,Human_RBP_ID_5357196,Human_RBP_ID_9324740,Human_RBP_ID_18982848,Human_RBP_ID_19070369,Human_RBP_ID_23256621,Human_RBP_ID_26768838 Human_Splice_Rec_1655790,Human_Splice_Rec_1655791,Human_Splice_Rec_1655805,Human_Splice_Rec_1655830,Human_Splice_Rec_1655831,Human_Splice_Rec_1655846,Human_Splice_Rec_1655887,Human_Splice_Rec_1655900,Human_Splice_Rec_1655901,Human_Splice_Rec_1655922,Human_Splice_Rec_1655938 RMVar_hsa_circ_123811,RMVar_hsa_circ_175417,RMVar_hsa_circ_86376,RMVar_hsa_circ_175425 72569 RMVar_ID_72569 Human_SNP_ID_590644326 m1A Human chr16 - 684112 684112 684112 GGCCGGGGGCCGTGGCGGAGGAGGAGCGCTGCACGGTGGAGCGTCGGGCCGACCTCACCTACGCG GGCCGGGGGCCGTGGCGGAGGAGGAGCGCTGCCCGGTGGAGCGTCGGGCCGACCTCACCTACGCG T G JMJD8 Ensembl:ENSG00000161999 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:684101..684325 26863196 MeRIP-seq:(Medium) rs745348274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761706,Human_RBP_ID_891053,Human_RBP_ID_5316420,Human_RBP_ID_5357196,Human_RBP_ID_9324740,Human_RBP_ID_18982848,Human_RBP_ID_19070369,Human_RBP_ID_23256621,Human_RBP_ID_26768838 Human_Splice_Rec_1655790,Human_Splice_Rec_1655791,Human_Splice_Rec_1655805,Human_Splice_Rec_1655830,Human_Splice_Rec_1655831,Human_Splice_Rec_1655846,Human_Splice_Rec_1655887,Human_Splice_Rec_1655900,Human_Splice_Rec_1655901,Human_Splice_Rec_1655922,Human_Splice_Rec_1655938 RMVar_hsa_circ_123811,RMVar_hsa_circ_175417,RMVar_hsa_circ_86376,RMVar_hsa_circ_175425 72570 RMVar_ID_72570 Human_SNP_ID_590644364 m1A Human chr16 - 684157 684157 684157 GGCGGGGCGCGGGCTGACCCAGCTGTGCCCGCAGGCGCCCGGGCGGGCCGGGGGCCGTGGCGGAG GGCGGGGCGCGGGCTGACCCAGCTGTGCCCGCGGGCGCCCGGGCGGGCCGGGGGCCGTGGCGGAG T C JMJD8 Ensembl:ENSG00000161999 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr16:684147..684325;chr16:684051..684263;chr16:684101..684251 26863196,26863410,26863410 MeRIP-seq:(Medium) rs919245426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891053,Human_RBP_ID_3948363,Human_RBP_ID_4383283,Human_RBP_ID_5113779,Human_RBP_ID_5357196,Human_RBP_ID_8184000,Human_RBP_ID_9324740,Human_RBP_ID_18982848,Human_RBP_ID_19070369,Human_RBP_ID_22652727,Human_RBP_ID_23256621,Human_RBP_ID_26768838,Human_RBP_ID_26779949 Human_Splice_Rec_1655791,Human_Splice_Rec_1655805,Human_Splice_Rec_1655831,Human_Splice_Rec_1655887,Human_Splice_Rec_1655901 RMVar_hsa_circ_86376,RMVar_hsa_circ_175425 72571 RMVar_ID_72571 Human_SNP_ID_590646985 m1A Human chr16 - 690147 690147 690147 CCTTGACGTCCCTCTGGGCCCTTCCCGCGTCTATCGCCTGAGTCCCCGGGCCCCTCTAGCCCTCT CCTTGACGTCCCTCTGGGCCCTTCCCGCGTCTGTCGCCTGAGTCCCCGGGCCCCTCTAGCCCTCT T C WDR24 Ensembl:ENSG00000127580 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:690144..690280 26863196 MeRIP-seq:(Medium) rs1047058557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393411,Human_RBP_ID_5440838,Human_RBP_ID_18684285 72572 RMVar_ID_72572 Human_SNP_ID_590648101 m1A Human chr16 - 693664 693664 693664 AGCCATGGCCCGCCGCCGAGAGCCCAGGCCCCACCCGCACCTCCTCACCCATCCAGCCTGACCCA AGCCATGGCCCGCCGCCGAGAGCCCAGGCCCCGCCCGCACCTCCTCACCCATCCAGCCTGACCCA T C FBXL16 Ensembl:ENSG00000127585 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:693617..694076 26863196 MeRIP-seq:(Medium) rs889151518 Functional Loss SNV dbSNP153 33..33 33 - - - 72573 RMVar_ID_72573 Human_SNP_ID_590648173 m1A Human chr16 - 693868 693866 693868 CCAGACTGTGCCCTTACCGCCTTCCCCGCCACACCCGCTCTGTCTTCCCACTGTCCCCCCCATCC CCAGACTGTGCCCTTACCGCCTTCCCCGCCAC__CCGCTCTGTCTTCCCACTGTCCCCCCCATCC GGT G FBXL16 Ensembl:ENSG00000127585 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:693843..694051 26863196 MeRIP-seq:(Medium) rs1323298743 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18178670,Human_RBP_ID_27445506 72574 RMVar_ID_72574 Human_SNP_ID_590648174 m1A Human chr16 - 693868 693868 693868 CCAGACTGTGCCCTTACCGCCTTCCCCGCCACACCCGCTCTGTCTTCCCACTGTCCCCCCCATCC CCAGACTGTGCCCTTACCGCCTTCCCCGCCACTCCCGCTCTGTCTTCCCACTGTCCCCCCCATCC T A FBXL16 Ensembl:ENSG00000127585 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:693843..694051 26863196 MeRIP-seq:(Medium) rs1402032899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18178670,Human_RBP_ID_27445506 72575 RMVar_ID_72575 Human_SNP_ID_590649560 m1A Human chr16 - 697380 697380 697380 CAGGAAGATGTCGAGCCCGGGCATCGACGGCGACCCCAAGCCTCCATGCTTGCCTCGAAACGGTC CAGGAAGATGTCGAGCCCGGGCATCGACGGCGGCCCCAAGCCTCCATGCTTGCCTCGAAACGGTC T C FBXL16 Ensembl:ENSG00000127585 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:697287..705580 32194978 MeRIP-seq:(Medium) rs1374954732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384125 Human_Splice_Rec_1656012,Human_Splice_Rec_1656022 RMVar_hsa_circ_175430,RMVar_hsa_circ_290302 72576 RMVar_ID_72576 Human_SNP_ID_590651008 m1A Human chr16 - 702163 702163 702163 AGGGGCCGGAGCTGAGGTCTCCGGGCTCAGTGACTTGATTCGCAGAAGAGGCAGCTCCTGCGGGG AGGGGCCGGAGCTGAGGTCTCCGGGCTCAGTGTCTTGATTCGCAGAAGAGGCAGCTCCTGCGGGG T A FBXL16 Ensembl:ENSG00000127585 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:702161..702390 26863196 MeRIP-seq:(Medium) rs1279179322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17690836 72577 RMVar_ID_72577 Human_SNP_ID_590651310 m1A Human chr16 + 703230 703230 703230 AAGTACTGCCCTCATCCTGCAGGGTCCCTGCCACGGCGCTGCATTCCTTGCAGAGGCTGCACACC AAGTACTGCCCTCATCCTGCAGGGTCCCTGCCGCGGCGCTGCATTCCTTGCAGAGGCTGCACACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:703221..703359 26863196 MeRIP-seq:(Medium) rs56301503 Functional Loss SNV dbSNP153 33..33 33 - - - 72578 RMVar_ID_72578 Human_SNP_ID_590651772 m1A Human chr16 - 704948 704948 704948 CTTGGCCAAGGTTGGAGGGCCTCAGAAGGGAAACGGCACCTTCAGACCTGCTCGGGAGGGGTCCG CTTGGCCAAGGTTGGAGGGCCTCAGAAGGGAATCGGCACCTTCAGACCTGCTCGGGAGGGGTCCG T A FBXL16 Ensembl:ENSG00000127585 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:704943..705200 26863196 MeRIP-seq:(Medium) rs1045470702 Functional Loss SNV dbSNP153 33..33 33 - - - 72579 RMVar_ID_72579 Human_SNP_ID_590655061 m1A Human chr16 + 715226 715226 715226 CGGCGCCCCCGGCTGCTCCCGCCGCCGCCCGGACCCGCGCCCCGCCGGGGCAGCGGTGGTGAGAG CGGCGCCCCCGGCTGCTCCCGCCGCCGCCCGGGCCCGCGCCCCGCCGGGGCAGCGGTGGTGAGAG A G METRN Ensembl:ENSG00000103260 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:715131..715265 26863410 MeRIP-seq:(Medium) rs1260760300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818671,Human_RBP_ID_4392718,Human_RBP_ID_5236448 RMVar_hsa_circ_125208,RMVar_hsa_circ_175431 72580 RMVar_ID_72580 Human_SNP_ID_590655073 m1A Human chr16 + 715264 715264 715264 GCCCCGCCGGGGCAGCGGTGGTGAGAGCCCCGACTCCCCGGACGCCGCCCGCCGTGCCATGGGGT GCCCCGCCGGGGCAGCGGTGGTGAGAGCCCCGGCTCCCCGGACGCCGCCCGCCGTGCCATGGGGT A G METRN Ensembl:ENSG00000103260 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:715114..716036;chr16:715126..715440;chr16:715147..715435;chr16:715161..715447 26863196 MeRIP-seq:(Medium) rs1033982236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393415,Human_RBP_ID_5237170,Human_RBP_ID_9325689 RMVar_hsa_circ_125208,RMVar_hsa_circ_175431 72581 RMVar_ID_72581 Human_SNP_ID_590655074 m1A Human chr16 - 715266 715266 715266 GAACCCCATGGCACGGCGGGCGGCGTCCGGGGAGTCGGGGCTCTCACCACCGCTGCCCCGGCGGG GAACCCCATGGCACGGCGGGCGGCGTCCGGGGGGTCGGGGCTCTCACCACCGCTGCCCCGGCGGG T C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr16:715164..715604 26863410 MeRIP-seq:(Medium) rs1233313193 Functional Loss SNV dbSNP153 33..33 33 - - - 72582 RMVar_ID_72582 Human_SNP_ID_590655198 m1A Human chr16 + 715543 715543 715543 TCGGGAGGGAGCGGGGGCTGCGCCGGGCGGGGACCCGCCCCCGTCTCAGCGCCCCGTCCCGTCCT TCGGGAGGGAGCGGGGGCTGCGCCGGGCGGGGCCCCGCCCCCGTCTCAGCGCCCCGTCCCGTCCT A C METRN Ensembl:ENSG00000103260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:715538..715664 26863196 MeRIP-seq:(Medium) rs1250952240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26779951 RMVar_hsa_circ_125208,RMVar_hsa_circ_175431 72583 RMVar_ID_72583 Human_SNP_ID_590655225 m1A Human chr16 + 715591 715591 715591 GCGCCCCGTCCCGTCCTGTCCCCAGCGGCCTCACCCAGGAGCCCGGCAGCGTGGGGCAGCTGGCC GCGCCCCGTCCCGTCCTGTCCCCAGCGGCCTCGCCCAGGAGCCCGGCAGCGTGGGGCAGCTGGCC A G METRN Ensembl:ENSG00000103260 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:715584..715692 26863196 MeRIP-seq:(Medium) rs892921377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384928 Human_Splice_Rec_1656044,Human_Splice_Rec_1656056 RMVar_hsa_circ_76272,RMVar_hsa_circ_125208,RMVar_hsa_circ_175431,RMVar_hsa_circ_175432 72584 RMVar_ID_72584 Human_SNP_ID_590655397 m1A Human chr16 + 715961 715960 715961 GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGCAGGCCCACGGTCTCGGCGTAGACGGTGAGTGGC GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGC_GGCCCACGGTCTCGGCGTAGACGGTGAGTGGC CA C METRN Ensembl:ENSG00000103260 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:715239..716445 32194978 MeRIP-seq:(Medium) rs767470797 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_233434,Human_RBP_ID_479878,Human_RBP_ID_760952,Human_RBP_ID_4392722,Human_RBP_ID_18189746,Human_RBP_ID_26809796 Human_Splice_Rec_1656045,Human_Splice_Rec_1656050,Human_Splice_Rec_1656051,Human_Splice_Rec_1656057,Human_Splice_Rec_1656059 RMVar_hsa_circ_76272,RMVar_hsa_circ_125208,RMVar_hsa_circ_175431,RMVar_hsa_circ_175432 72585 RMVar_ID_72585 Human_SNP_ID_590655398 m1A Human chr16 + 715961 715961 715961 GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGCAGGCCCACGGTCTCGGCGTAGACGGTGAGTGGC GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGCGGGCCCACGGTCTCGGCGTAGACGGTGAGTGGC A G METRN Ensembl:ENSG00000103260 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:715239..716445 32194978 MeRIP-seq:(Medium) rs1392849676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233434,Human_RBP_ID_479878,Human_RBP_ID_760952,Human_RBP_ID_4392722,Human_RBP_ID_18189746,Human_RBP_ID_26809796 Human_Splice_Rec_1656045,Human_Splice_Rec_1656050,Human_Splice_Rec_1656051,Human_Splice_Rec_1656057,Human_Splice_Rec_1656059 RMVar_hsa_circ_76272,RMVar_hsa_circ_125208,RMVar_hsa_circ_175431,RMVar_hsa_circ_175432 72586 RMVar_ID_72586 Human_SNP_ID_590655399 m1A Human chr16 + 715961 715961 715961 GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGCAGGCCCACGGTCTCGGCGTAGACGGTGAGTGGC GCGCGAGGACGGGCGCCCCGAGCTGCCCCCGCTGGCCCACGGTCTCGGCGTAGACGGTGAGTGGC A T METRN Ensembl:ENSG00000103260 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:715239..716445 32194978 MeRIP-seq:(Medium) rs1392849676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233434,Human_RBP_ID_479878,Human_RBP_ID_760952,Human_RBP_ID_4392722,Human_RBP_ID_18189746,Human_RBP_ID_26809796 Human_Splice_Rec_1656045,Human_Splice_Rec_1656050,Human_Splice_Rec_1656051,Human_Splice_Rec_1656057,Human_Splice_Rec_1656059 RMVar_hsa_circ_76272,RMVar_hsa_circ_125208,RMVar_hsa_circ_175431,RMVar_hsa_circ_175432 72587 RMVar_ID_72587 Human_SNP_ID_590655894 m1A Human chr16 - 717213 717213 717213 CCCGGGTGGACGCCACAGCGCAGTGGGGTACGAATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC CCCGGGTGGACGCCACAGCGCAGTGGGGTACGTATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC T A lnc-CCDC78-4 RNACentral:URS0000D5A077 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:717092..717425;chr16:717096..717380 26863196 MeRIP-seq:(Medium) rs755345356 Functional Loss SNV dbSNP153 33..33 33 - - - 72588 RMVar_ID_72588 Human_SNP_ID_590655895 m1A Human chr16 - 717213 717213 717213 CCCGGGTGGACGCCACAGCGCAGTGGGGTACGAATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC CCCGGGTGGACGCCACAGCGCAGTGGGGTACGGATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC T C lnc-CCDC78-4 RNACentral:URS0000D5A077 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:717092..717425;chr16:717096..717380 26863196 MeRIP-seq:(Medium) rs755345356 Functional Loss SNV dbSNP153 33..33 33 - - - 72589 RMVar_ID_72589 Human_SNP_ID_590655896 m1A Human chr16 - 717213 717213 717213 CCCGGGTGGACGCCACAGCGCAGTGGGGTACGAATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC CCCGGGTGGACGCCACAGCGCAGTGGGGTACGCATGGAGGTCAGCCCCTGGTCCCCGGATCGCCC T G lnc-CCDC78-4 RNACentral:URS0000D5A077 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:717092..717425;chr16:717096..717380 26863196 MeRIP-seq:(Medium) rs755345356 Functional Loss SNV dbSNP153 33..33 33 - - - 72590 RMVar_ID_72590 Human_SNP_ID_590657337 m1A Human chr16 + 721208 721208 721208 GGAGGCAGAGGGCACACCGCCAGCCCCAGGCCAGGCTGCGAGGGCCGCGGACCCGAGCCGGGAAG GGAGGCAGAGGGCACACCGCCAGCCCCAGGCCGGGCTGCGAGGGCCGCGGACCCGAGCCGGGAAG A G ANTKMT Ensembl:ENSG00000103254 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:721151..721881;chr16:721151..721725;chr16:721151..721816;chr16:721151..721812 26863196 MeRIP-seq:(Medium) rs942897535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394207,Human_RBP_ID_5523860,Human_RBP_ID_8941316,Human_RBP_ID_18418630 72591 RMVar_ID_72591 Human_SNP_ID_590657976 m1A Human chr16 - 722310 722300 722310 GCTCTGTCCGCAGCTTGTCCTCCAGCAGCGGGAGCTGAGGGAGAGAACAGCAGAGTAGAGGGGGC GCTCTGTCCGCAGCTTGTCCTCCAGCAGCGGG__________GAGAACAGCAGAGTAGAGGGGGC CTCCCTCAGCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:722304..722502 32194978 MeRIP-seq:(Medium) rs1317062693 Functional Loss DEL dbSNP153 33..42 33 - - - 72592 RMVar_ID_72592 Human_SNP_ID_590660499 m1A Human chr16 + 727510 727510 727510 GGAGCAGGCACCGGTGGCCGAGCTCCGTGACCATGAAGGTCAAGGTCATCCCCGTGCTCGAGGAC GGAGCAGGCACCGGTGGCCGAGCTCCGTGACCTTGAAGGTCAAGGTCATCCCCGTGCTCGAGGAC A T HAGHL Ensembl:ENSG00000103253 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:727067..728104 26863196 MeRIP-seq:(Medium) rs955322438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234721,Human_RBP_ID_890179,Human_RBP_ID_3946928,Human_RBP_ID_17121324,Human_RBP_ID_18684863,Human_RBP_ID_22051775 Human_Splice_Rec_1656324,Human_Splice_Rec_1656334,Human_Splice_Rec_1656346,Human_Splice_Rec_1656348,Human_Splice_Rec_1656358 72593 RMVar_ID_72593 Human_SNP_ID_590661386 m1A Human chr16 + 729025 729025 729025 CCTGTGGTCACTCCAGAAGAGGGATGAGGATGACGTGCCCACTGTGCCGTCGACTCTGGGCGAGG CCTGTGGTCACTCCAGAAGAGGGATGAGGATGGCGTGCCCACTGTGCCGTCGACTCTGGGCGAGG A G HAGHL Ensembl:ENSG00000103253 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:728983..729215 26863196 MeRIP-seq:(Medium) rs776454569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502279,Human_RBP_ID_3946929,Human_RBP_ID_5113787,Human_RBP_ID_9324752,Human_RBP_ID_18163176,Human_RBP_ID_22944787 Human_Splice_Rec_1656393,Human_Splice_Rec_1656425 72594 RMVar_ID_72594 Human_SNP_ID_590665864 m1A Human chr16 + 740872 740872 740872 AAGTGGGGCGCAGAGCAATTTCCCTCCGCGCGACAGGGCACCGAGCGCAGCCTCGACCCCGCCCG AAGTGGGGCGCAGAGCAATTTCCCTCCGCGCGGCAGGGCACCGAGCGCAGCCTCGACCCCGCCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:740868..740968 26863196 MeRIP-seq:(Medium) rs1211026672 Functional Loss SNV dbSNP153 33..33 33 - - - 72595 RMVar_ID_72595 Human_SNP_ID_590667980 m1A Human chr16 - 746523 746483 746523 TGAACCCACCTCCTCTCCTGCAGCCCGCCCAGACAGACCCGCAGTGACCCCACCTCCTCTCCTGC TGAACCCACCTCCTCTCCTGCAGCCCGCCCAG_________________________________ GGCGGGCTGCAGGAGAGGAGGTGGGGTCACTGCGGGTCTGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:746519..746846 26863196 MeRIP-seq:(Medium) rs1471162421 Functional Loss DEL dbSNP153 33..65 33 - - - 72596 RMVar_ID_72596 Human_SNP_ID_590667986 m1A Human chr16 + 746498 746498 746498 CACTGCAGGTCTGTCTGGGCGGGCTGCAGGAGAGGAGGTGGGGTCACTGCGGGTCTGTCTGGGCG CACTGCAGGTCTGTCTGGGCGGGCTGCAGGAGGGGAGGTGGGGTCACTGCGGGTCTGTCTGGGCG A G lnc-MSLN-2 RNACentral:URS0000D5C2D1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:746406..746765 26863196 MeRIP-seq:(Medium) rs1477894432 Functional Loss SNV dbSNP153 33..33 33 - - - 72597 RMVar_ID_72597 Human_SNP_ID_590668002 m1A Human chr16 - 746523 746522 746523 TGAACCCACCTCCTCTCCTGCAGCCCGCCCAGACAGACCCGCAGTGACCCCACCTCCTCTCCTGC TGAACCCACCTCCTCTCCTGCAGCCCGCCCAG_CAGACCCGCAGTGACCCCACCTCCTCTCCTGC GT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:746519..746846 26863196 MeRIP-seq:(Medium) rs1216585277 Functional Loss DEL dbSNP153 33..33 33 - - - 72598 RMVar_ID_72598 Human_SNP_ID_590668003 m1A Human chr16 - 746523 746523 746523 TGAACCCACCTCCTCTCCTGCAGCCCGCCCAGACAGACCCGCAGTGACCCCACCTCCTCTCCTGC TGAACCCACCTCCTCTCCTGCAGCCCGCCCAGGCAGACCCGCAGTGACCCCACCTCCTCTCCTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:746519..746846 26863196 MeRIP-seq:(Medium) rs1257017433 Functional Loss SNV dbSNP153 33..33 33 - - - 72599 RMVar_ID_72599 Human_SNP_ID_590673541 m1A Human chr16 + 762654 762654 762654 GGCGTGGGGTGGGAGCAGGGGGTCCCATCCTGAGTCACTGCCCTCCACAGACACAGACCATGGCC GGCGTGGGGTGGGAGCAGGGGGTCCCATCCTGCGTCACTGCCCTCCACAGACACAGACCATGGCC A C MSLN Ensembl:ENSG00000102854 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:762651..762700;chr16:762651..762725 26863196 MeRIP-seq:(Medium) rs745592949 Functional Loss SNV dbSNP153 33..33 33 - - - 72600 RMVar_ID_72600 Human_SNP_ID_590674146 m1A Human chr16 - 764073 764073 764073 CCACAGCCAGCTCCCGGACACGCTCCGTGCTCAGGCCGGACACCTCCGCACACGGGAAGCCAAGG CCACAGCCAGCTCCCGGACACGCTCCGTGCTCGGGCCGGACACCTCCGCACACGGGAAGCCAAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:763991..764172;chr16:763943..764175 26863196 MeRIP-seq:(Medium) rs752384917 Functional Loss SNV dbSNP153 33..33 33 - - - 72601 RMVar_ID_72601 Human_SNP_ID_590674488 m1A Human chr16 - 764866 764866 764866 AGAGGGTGCTGGGGACAGGCCGCACTGATCACACCCGTCCCCACCCTGAGAGGCAGCCCGGCCGG AGAGGGTGCTGGGGACAGGCCGCACTGATCACGCCCGTCCCCACCCTGAGAGGCAGCCCGGCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:764862..764979 26863196 MeRIP-seq:(Medium) rs1462119755 Functional Loss SNV dbSNP153 33..33 33 - - - 72602 RMVar_ID_72602 Human_SNP_ID_590675543 m1A Human chr16 - 766807 766807 766807 CCTTGCCGGGCAGAGTTCTGGGGACTCACCAGATGCTGCTGGGGGGCACGGAGCTCAGCTCCTCG CCTTGCCGGGCAGAGTTCTGGGGACTCACCAGGTGCTGCTGGGGGGCACGGAGCTCAGCTCCTCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:766757..766880 26863196 MeRIP-seq:(Medium) rs749650942 Functional Loss SNV dbSNP153 33..33 33 - - - 72603 RMVar_ID_72603 Human_SNP_ID_590675916 m1A Human chr16 - 767469 767469 767469 CTCCACACGCCCCTCCTCCCGCTCGCCATACCAGCACCGCATCCGTCCGCAGCTTCATGAACGTG CTCCACACGCCCCTCCTCCCGCTCGCCATACCGGCACCGCATCCGTCCGCAGCTTCATGAACGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:767344..767527 26863196 MeRIP-seq:(Medium) rs1424733876 Functional Loss SNV dbSNP153 33..33 33 - - - 72604 RMVar_ID_72604 Human_SNP_ID_590676899 m1A Human chr16 - 768152 768152 768152 GCTGCCCTTCCTAAGGCCTCGCCCCACTGCAGACCCGCCTTACACGCCCTCCCACCCCCCGTTGG GCTGCCCTTCCTAAGGCCTCGCCCCACTGCAGGCCCGCCTTACACGCCCTCCCACCCCCCGTTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:768147..768643 26863196 MeRIP-seq:(Medium) rs1425940398 Functional Loss SNV dbSNP153 33..33 33 - - - 72605 RMVar_ID_72605 Human_SNP_ID_590677267 m1A Human chr16 - 768751 768751 768751 GCCAGGCGGGGATCCCCAGCAGGGCTGGGGCCAGCAAGGGAGTGGGGCCCTCAGGCCAGGGTGGA GCCAGGCGGGGATCCCCAGCAGGGCTGGGGCCGGCAAGGGAGTGGGGCCCTCAGGCCAGGGTGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:768701..769107 26863196 MeRIP-seq:(Medium) rs1463281001 Functional Loss SNV dbSNP153 33..33 33 - - - 72606 RMVar_ID_72606 Human_SNP_ID_590677278 m1A Human chr16 - 768766 768766 768766 CCGTGCCTGCTCCTGGCCAGGCGGGGATCCCCAGCAGGGCTGGGGCCAGCAAGGGAGTGGGGCCC CCGTGCCTGCTCCTGGCCAGGCGGGGATCCCCGGCAGGGCTGGGGCCAGCAAGGGAGTGGGGCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:768751..768775 26863196 MeRIP-seq:(Medium) rs759590887 Functional Loss SNV dbSNP153 33..33 33 - - - 72607 RMVar_ID_72607 Human_SNP_ID_590677279 m1A Human chr16 - 768766 768766 768766 CCGTGCCTGCTCCTGGCCAGGCGGGGATCCCCAGCAGGGCTGGGGCCAGCAAGGGAGTGGGGCCC CCGTGCCTGCTCCTGGCCAGGCGGGGATCCCCCGCAGGGCTGGGGCCAGCAAGGGAGTGGGGCCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:768751..768775 26863196 MeRIP-seq:(Medium) rs759590887 Functional Loss SNV dbSNP153 33..33 33 - - - 72608 RMVar_ID_72608 Human_SNP_ID_590678674 m1A Human chr16 - 770900 770900 770900 GCCCCCAGAGCCGGAAGGACGTGCTCTACACCAAGGCCCATGAGACCTTCGGCAGCAGCGGGACC GCCCCCAGAGCCGGAAGGACGTGCTCTACACCGAGGCCCATGAGACCTTCGGCAGCAGCGGGACC T C MSLNL Ensembl:ENSG00000162006 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:770897..771151 26863196 MeRIP-seq:(Medium) rs1190549040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1656830,Human_Splice_Rec_1656831,Human_Splice_Rec_1656854,Human_Splice_Rec_1656855 72609 RMVar_ID_72609 Human_SNP_ID_590680264 m1A Human chr16 + 774684 774684 774684 TGCCCCCACCACAGCCAGCGGGACAGCACCCCAACCCTCTGCCCCCTCGGCCGCAGGACCCAGTG TGCCCCCACCACAGCCAGCGGGACAGCACCCCCACCCTCTGCCCCCTCGGCCGCAGGACCCAGTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:774671..774801 26863196 MeRIP-seq:(Medium) rs1429501337 Functional Loss SNV dbSNP153 33..33 33 - - - 72610 RMVar_ID_72610 Human_SNP_ID_590680477 m1A Human chr16 - 775071 775071 775071 TGGTGGGCGCCTGGGCAGGATGGGCCCGGTGCATTGGAGGCAGCCTCCCGCTGGGCGCCGACCTG TGGTGGGCGCCTGGGCAGGATGGGCCCGGTGCGTTGGAGGCAGCCTCCCGCTGGGCGCCGACCTG T C MSLNL Ensembl:ENSG00000162006 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:775043..775283 26863196 MeRIP-seq:(Medium) rs1244303142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1656818 72611 RMVar_ID_72611 Human_SNP_ID_590684957 m1A Human chr16 + 785078 785078 785078 GCATGGGGGACAGAGGAGGTGGGACCTGGCAGACCCACAGCTCCCAAGCTGGGGTCCCGGAGGCA GCATGGGGGACAGAGGAGGTGGGACCTGGCAGGCCCACAGCTCCCAAGCTGGGGTCCCGGAGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:785045..785140 26863196 MeRIP-seq:(Medium) rs545335133 Functional Loss SNV dbSNP153 33..33 33 - - - 72612 RMVar_ID_72612 Human_SNP_ID_590684962 m1A Human chr16 - 785087 785087 785087 TTGTCACTCTGCCTCCGGGACCCCAGCTTGGGAGCTGTGGGTCTGCCAGGTCCCACCTCCTCTGT TTGTCACTCTGCCTCCGGGACCCCAGCTTGGGGGCTGTGGGTCTGCCAGGTCCCACCTCCTCTGT T C RPUSD1 Ensembl:ENSG00000007376 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:785052..785209;chr16:785039..785246 26863196 MeRIP-seq:(Medium) rs527884358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480364,Human_RBP_ID_27246497,Human_RBP_ID_27446015 Human_miRNA_ID_340876,Human_miRNA_ID_1693246,Human_miRNA_ID_1954746,Human_miRNA_ID_2086741,Human_miRNA_ID_3061715 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443 72613 RMVar_ID_72613 Human_SNP_ID_590685151 m1A Human chr16 + 785465 785465 785465 GGCAGAGGACGCAGGGACCAGATGGGTCTCCCAGGCCAGGTGAGCCCAGAACGGCCCTTCCCAGC GGCAGAGGACGCAGGGACCAGATGGGTCTCCCGGGCCAGGTGAGCCCAGAACGGCCCTTCCCAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:785418..785814 32194978 MeRIP-seq:(Medium) rs1257637614 Functional Loss SNV dbSNP153 33..33 33 - - - 72614 RMVar_ID_72614 Human_SNP_ID_590685391 m1A Human chr16 - 785962 785961 785962 TGCCTGCAGTGGCTGTCGGAGTGGACGCTGGAACCGGACAGCTGAGAGCCGTGGGGCTGGGGCAG TGCCTGCAGTGGCTGTCGGAGTGGACGCTGGA_CCGGACAGCTGAGAGCCGTGGGGCTGGGGCAG GT G RPUSD1 Ensembl:ENSG00000007376 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:785911..786250 26863196 MeRIP-seq:(Medium) rs1490836654 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_480378,Human_RBP_ID_23702666,Human_RBP_ID_27246509,Human_RBP_ID_27446026 Human_miRNA_ID_3002748 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443 72615 RMVar_ID_72615 Human_SNP_ID_590685403 m1A Human chr16 + 785981 785980 785981 CTCAGCTGTCCGGTTCCAGCGTCCACTCCGACAGCCACTGCAGGCAGGGGCCCCGCTGTGCCTCA CTCAGCTGTCCGGTTCCAGCGTCCACTCCGAC_GCCACTGCAGGCAGGGGCCCCGCTGTGCCTCA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:785930..786237 26863196 MeRIP-seq:(Medium) rs774826129 Functional Loss DEL dbSNP153 33..33 33 - - - 72616 RMVar_ID_72616 Human_SNP_ID_590685406 m1A Human chr16 + 785981 785981 785981 CTCAGCTGTCCGGTTCCAGCGTCCACTCCGACAGCCACTGCAGGCAGGGGCCCCGCTGTGCCTCA CTCAGCTGTCCGGTTCCAGCGTCCACTCCGACGGCCACTGCAGGCAGGGGCCCCGCTGTGCCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:785930..786237 26863196 MeRIP-seq:(Medium) rs1314240428 Functional Loss SNV dbSNP153 33..33 33 - - - 72617 RMVar_ID_72617 Human_SNP_ID_590685408 m1A Human chr16 + 785985 785985 785985 GCTGTCCGGTTCCAGCGTCCACTCCGACAGCCACTGCAGGCAGGGGCCCCGCTGTGCCTCAGTCT GCTGTCCGGTTCCAGCGTCCACTCCGACAGCCGCTGCAGGCAGGGGCCCCGCTGTGCCTCAGTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:785951..786189 26863196 MeRIP-seq:(Medium) rs1355629728 Functional Loss SNV dbSNP153 33..33 33 - - - 72618 RMVar_ID_72618 Human_SNP_ID_590685652 m1A Human chr16 - 786348 786348 786348 CAGGCCGGACACACCAGCTGCGCGTGCACTGCAGTGCCCTGGGCCACCCCGTGGTGGGCGACCTG CAGGCCGGACACACCAGCTGCGCGTGCACTGCGGTGCCCTGGGCCACCCCGTGGTGGGCGACCTG T C RPUSD1 Ensembl:ENSG00000007376 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:786110..786358 32194978 MeRIP-seq:(Medium) rs368730340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1656876,Human_Splice_Rec_1656886,Human_Splice_Rec_1656894,Human_Splice_Rec_1656902,Human_Splice_Rec_1656910,Human_Splice_Rec_1656920,Human_Splice_Rec_1656930 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443 72619 RMVar_ID_72619 Human_SNP_ID_590686446 m1A Human chr16 - 787407 787407 787407 TGTGCGTGGCCCTAAACAAGGCAGCCGCCGGCAGCGCGTACAGGTGCTTCAAGGAGCGGCGCGTG TGTGCGTGGCCCTAAACAAGGCAGCCGCCGGCGGCGCGTACAGGTGCTTCAAGGAGCGGCGCGTG T C RPUSD1 Ensembl:ENSG00000007376 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:787139..787452 26863410 MeRIP-seq:(Medium) rs878980150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1656870,Human_Splice_Rec_1656871,Human_Splice_Rec_1656880,Human_Splice_Rec_1656881,Human_Splice_Rec_1656890,Human_Splice_Rec_1656891,Human_Splice_Rec_1656896,Human_Splice_Rec_1656897,Human_Splice_Rec_1656906,Human_Splice_Rec_1656907,Human_Splice_Rec_1656914,Human_Splice_Rec_1656915,Human_Splice_Rec_1656924,Human_Splice_Rec_1656925,Human_Splice_Rec_1656931,Human_Splice_Rec_1656938,Human_Splice_Rec_1656939,Human_Splice_Rec_1656946,Human_Splice_Rec_1656947 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443,RMVar_hsa_circ_101555,RMVar_hsa_circ_175445 72620 RMVar_ID_72620 Human_SNP_ID_590686654 m1A Human chr16 - 787674 787674 787674 TCGTGTACCGGAGCCGCGACTTCCTGGTGGTCAACAAGCACTGGGACGTTCGCATTGACAGCAAG TCGTGTACCGGAGCCGCGACTTCCTGGTGGTCTACAAGCACTGGGACGTTCGCATTGACAGCAAG T A RPUSD1 Ensembl:ENSG00000007376 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:787640..787789 26863196 MeRIP-seq:(Medium) rs1421019755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393426 Human_Splice_Rec_1656878,Human_Splice_Rec_1656888,Human_Splice_Rec_1656922,Human_Splice_Rec_1656936,Human_Splice_Rec_1656944 Human_miRNA_ID_2843790 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443 72621 RMVar_ID_72621 Human_SNP_ID_590686655 m1A Human chr16 - 787674 787674 787674 TCGTGTACCGGAGCCGCGACTTCCTGGTGGTCAACAAGCACTGGGACGTTCGCATTGACAGCAAG TCGTGTACCGGAGCCGCGACTTCCTGGTGGTCGACAAGCACTGGGACGTTCGCATTGACAGCAAG T C RPUSD1 Ensembl:ENSG00000007376 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:787640..787789 26863196 MeRIP-seq:(Medium) rs1421019755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393426 Human_Splice_Rec_1656878,Human_Splice_Rec_1656888,Human_Splice_Rec_1656922,Human_Splice_Rec_1656936,Human_Splice_Rec_1656944 Human_miRNA_ID_2843790 RMVar_hsa_circ_106985,RMVar_hsa_circ_175443 72622 RMVar_ID_72622 Human_SNP_ID_590687021 m1A Human chr16 - 788328 788303 788328 CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGCCAGCGCGCGGGCGCGCGGCTGGAGCCGGCGCCGG CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGCC_________________________GGCGCCGG CGGCTCCAGCCGCGCGCCCGCGCGCT C RPUSD1 Ensembl:ENSG00000007376 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:788203..788346;chr16:788064..788375 26863196 MeRIP-seq:(Medium) rs1404179234 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_4393428,Human_RBP_ID_5496207,Human_RBP_ID_18418864,Human_RBP_ID_22944936 Human_Splice_Rec_1656877,Human_Splice_Rec_1656887,Human_Splice_Rec_1656895,Human_Splice_Rec_1656903,Human_Splice_Rec_1656911,Human_Splice_Rec_1656921,Human_Splice_Rec_1656935,Human_Splice_Rec_1656943 72623 RMVar_ID_72623 Human_SNP_ID_590687032 m1A Human chr16 - 788328 788315 788329 CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGCCAGCGCGCGGGCGCGCGGCTGGAGCCGGCGCCGG CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGC______________GCGGCTGGAGCCGGCGCCGG CGCGCCCGCGCGCTG C RPUSD1 Ensembl:ENSG00000007376 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:788203..788346;chr16:788064..788375 26863196 MeRIP-seq:(Medium) rs1457183467 Functional Loss DEL dbSNP153 32..45 33 - - - Human_RBP_ID_4393428,Human_RBP_ID_5496207,Human_RBP_ID_18418864,Human_RBP_ID_22944936 Human_Splice_Rec_1656877,Human_Splice_Rec_1656887,Human_Splice_Rec_1656895,Human_Splice_Rec_1656903,Human_Splice_Rec_1656911,Human_Splice_Rec_1656921,Human_Splice_Rec_1656935,Human_Splice_Rec_1656943 72624 RMVar_ID_72624 Human_SNP_ID_590687042 m1A Human chr16 - 788328 788328 788328 CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGCCAGCGCGCGGGCGCGCGGCTGGAGCCGGCGCCGG CGGAGCGGAGCTTCCAGGGTCTCTGGGTCGCCGGCGCGCGGGCGCGCGGCTGGAGCCGGCGCCGG T C RPUSD1 Ensembl:ENSG00000007376 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:788203..788346;chr16:788064..788375 26863196 MeRIP-seq:(Medium) rs1158869166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393428,Human_RBP_ID_5496207,Human_RBP_ID_18418864,Human_RBP_ID_22944936 Human_Splice_Rec_1656877,Human_Splice_Rec_1656887,Human_Splice_Rec_1656895,Human_Splice_Rec_1656903,Human_Splice_Rec_1656911,Human_Splice_Rec_1656921,Human_Splice_Rec_1656935,Human_Splice_Rec_1656943 72625 RMVar_ID_72625 Human_SNP_ID_590687048 m1A Human chr16 + 788333 788333 788333 GCCGGCTCCAGCCGCGCGCCCGCGCGCTGGCGACCCAGAGACCCTGGAAGCTCCGCTCCGGACGC GCCGGCTCCAGCCGCGCGCCCGCGCGCTGGCGGCCCAGAGACCCTGGAAGCTCCGCTCCGGACGC A G CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:788058..788375;chr16:788227..788334 26863196 MeRIP-seq:(Medium) rs1262500651 Functional Loss SNV dbSNP153 33..33 33 - - - 72626 RMVar_ID_72626 Human_SNP_ID_590687338 m1A Human chr16 + 788701 788701 788701 CGGGCTCGCGGACGGTATGGAGGACTACGAGCAGGAGCTGTGCGGCGTCGAGGATGATTTCCACA CGGGCTCGCGGACGGTATGGAGGACTACGAGCGGGAGCTGTGCGGCGTCGAGGATGATTTCCACA A G CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:788651..789337 26863196 MeRIP-seq:(Medium) rs1442671542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22944937 Human_Splice_Rec_1656951,Human_Splice_Rec_1656995,Human_Splice_Rec_1657037,Human_Splice_Rec_1657071,Human_Splice_Rec_1657075,Human_Splice_Rec_1657081,Human_Splice_Rec_1657093,Human_Splice_Rec_1657133,Human_Splice_Rec_1657159,Human_Splice_Rec_1657201 72627 RMVar_ID_72627 Human_SNP_ID_590687375 m1A Human chr16 - 788739 788739 788739 CAGCTCTGCCAGCACCTCCAGCTCGGCCGCGAACTGGTTGTGGAAATCATCCTCGACGCCGCACA CAGCTCTGCCAGCACCTCCAGCTCGGCCGCGACCTGGTTGTGGAAATCATCCTCGACGCCGCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:788626..788800 26863196 MeRIP-seq:(Medium) rs780222004 Functional Loss SNV dbSNP153 33..33 33 - - - 72628 RMVar_ID_72628 Human_SNP_ID_590687594 m1A Human chr16 + 789063 789063 789063 TCCCGCCCCAGCCGCATCTGTGGGCAGCAGCCAGGGCGGCGCCAGGAAGAGGCAGGTGGACGCCG TCCCGCCCCAGCCGCATCTGTGGGCAGCAGCCGGGGCGGCGCCAGGAAGAGGCAGGTGGACGCCG A G CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:788688..789386 32194978 MeRIP-seq:(Medium) rs1210986444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891073 Human_Splice_Rec_1656953,Human_Splice_Rec_1656997,Human_Splice_Rec_1657039,Human_Splice_Rec_1657073,Human_Splice_Rec_1657077,Human_Splice_Rec_1657083,Human_Splice_Rec_1657135,Human_Splice_Rec_1657161,Human_Splice_Rec_1657203 72629 RMVar_ID_72629 Human_SNP_ID_590687942 m1A Human chr16 - 789526 789526 789526 GCTTCTGAGACTCTGGAGAGAGACCGGGGCTCAGTGGCAGAAACTCAAGCGTGGGGTCACCCTTG GCTTCTGAGACTCTGGAGAGAGACCGGGGCTCGGTGGCAGAAACTCAAGCGTGGGGTCACCCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:789524..789732 26863196 MeRIP-seq:(Medium) rs748089452 Functional Loss SNV dbSNP153 33..33 33 - - - 72630 RMVar_ID_72630 Human_SNP_ID_590687943 m1A Human chr16 - 789526 789526 789526 GCTTCTGAGACTCTGGAGAGAGACCGGGGCTCAGTGGCAGAAACTCAAGCGTGGGGTCACCCTTG GCTTCTGAGACTCTGGAGAGAGACCGGGGCTCCGTGGCAGAAACTCAAGCGTGGGGTCACCCTTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:789524..789732 26863196 MeRIP-seq:(Medium) rs748089452 Functional Loss SNV dbSNP153 33..33 33 - - - 72631 RMVar_ID_72631 Human_SNP_ID_590688003 m1A Human chr16 - 789595 789595 789595 ATGGGGGGCCGCCTCAGGACGGGATTGCGGGCAGCTGGTGAGGCCCGTGTGAGACCCACGTCGGC ATGGGGGGCCGCCTCAGGACGGGATTGCGGGCGGCTGGTGAGGCCCGTGTGAGACCCACGTCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:789526..789675 26863196 MeRIP-seq:(Medium) rs764092898 Functional Loss SNV dbSNP153 33..33 33 - - - 72632 RMVar_ID_72632 Human_SNP_ID_590688787 m1A Human chr16 + 790549 790549 790549 CTCTCCAGTCTCAGGTCGGGGGAGGAGGAGGCAGCCCAGCCCTTGGGGGCCCCTGAGGAGGAGCC CTCTCCAGTCTCAGGTCGGGGGAGGAGGAGGCTGCCCAGCCCTTGGGGGCCCCTGAGGAGGAGCC A T CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:790517..790595;chr16:790526..790622 26863196 MeRIP-seq:(Medium) rs541869124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761244,Human_RBP_ID_818262,Human_RBP_ID_3948378,Human_RBP_ID_5359052,Human_RBP_ID_18982864,Human_RBP_ID_22944542,Human_RBP_ID_26328388 Human_Splice_Rec_1656962,Human_Splice_Rec_1657006,Human_Splice_Rec_1657046,Human_Splice_Rec_1657092,Human_Splice_Rec_1657102,Human_Splice_Rec_1657144,Human_Splice_Rec_1657170,Human_Splice_Rec_1657212,Human_Splice_Rec_1657244,Human_Splice_Rec_1657256,Human_Splice_Rec_1657264,Human_Splice_Rec_1657268 Human_miRNA_ID_2295868,Human_miRNA_ID_2554555 RMVar_hsa_circ_95827,RMVar_hsa_circ_269155,RMVar_hsa_circ_175446 72633 RMVar_ID_72633 Human_SNP_ID_590688958 m1A Human chr16 + 790769 790769 790769 GATTTTTGCACAGCCAATCCACTGGGCCTCGGAGACGGAGTGGGCTCTGGTTTGCCCTTTTGAGT GATTTTTGCACAGCCAATCCACTGGGCCTCGGGGACGGAGTGGGCTCTGGTTTGCCCTTTTGAGT A G CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3765266 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_22052700 GWAS_ID_8855,GWAS_ID_8856,GWAS_ID_8857,GWAS_ID_8858,GWAS_ID_8859,GWAS_ID_8860 RMVar_hsa_circ_95827,RMVar_hsa_circ_269155,RMVar_hsa_circ_175446 72634 RMVar_ID_72634 Human_SNP_ID_590689017 m1A Human chr16 - 790894 790893 790895 CAGCTGCTGTGAAGGTAGGAAAGGGAACAGAGACTTGGATCAGGTGACACCCTGGACCCCTAGCC CAGCTGCTGTGAAGGTAGGAAAGGGAACAGA__CTTGGATCAGGTGACACCCTGGACCCCTAGCC GTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:790881..791122 26863196 MeRIP-seq:(Medium) rs1259225233 Functional Loss DEL dbSNP153 32..33 33 - - - 72635 RMVar_ID_72635 Human_SNP_ID_590689245 m1A Human chr16 + 791312 791312 791312 CACAGCCCCAGGCAAGTGGAAGAGCCACGAACAGGTGCTGGAGGAGATGCTGGAGGCTGGGCTGG CACAGCCCCAGGCAAGTGGAAGAGCCACGAACCGGTGCTGGAGGAGATGCTGGAGGCTGGGCTGG A C CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:791263..791345 26863196 MeRIP-seq:(Medium) rs765535375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1523471,Human_RBP_ID_4403971,Human_RBP_ID_9372022,Human_RBP_ID_18685481,Human_RBP_ID_22942927 Human_Splice_Rec_1656965,Human_Splice_Rec_1657009,Human_Splice_Rec_1657105,Human_Splice_Rec_1657147,Human_Splice_Rec_1657173,Human_Splice_Rec_1657271,Human_Splice_Rec_1657277,Human_Splice_Rec_1657279 Human_miRNA_ID_1979345,Human_miRNA_ID_2441925 RMVar_hsa_circ_7167,RMVar_hsa_circ_95827,RMVar_hsa_circ_269155,RMVar_hsa_circ_50940,RMVar_hsa_circ_175446 72636 RMVar_ID_72636 Human_SNP_ID_590689591 m1A Human chr16 + 791884 791884 791884 TGGCACTGCTCTGTGGGCCCCCGGGGCTGGGGAAGACCACCCTGGCACACGTGATTGCGCGTCAC TGGCACTGCTCTGTGGGCCCCCGGGGCTGGGGCAGACCACCCTGGCACACGTGATTGCGCGTCAC A C CHTF18 Ensembl:ENSG00000127586 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:791851..791981 26863196 MeRIP-seq:(Medium) rs751842837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233596,Human_RBP_ID_260938,Human_RBP_ID_891078,Human_RBP_ID_17121332,Human_RBP_ID_17669650,Human_RBP_ID_18481709,Human_RBP_ID_18982870,Human_RBP_ID_19070386,Human_RBP_ID_21971787,Human_RBP_ID_22053750,Human_RBP_ID_22944940,Human_RBP_ID_23703137,Human_RBP_ID_24370132,Human_RBP_ID_26769051,Human_RBP_ID_27837679 Human_Splice_Rec_1656966,Human_Splice_Rec_1656967,Human_Splice_Rec_1657010,Human_Splice_Rec_1657011,Human_Splice_Rec_1657106,Human_Splice_Rec_1657107,Human_Splice_Rec_1657148,Human_Splice_Rec_1657149,Human_Splice_Rec_1657174,Human_Splice_Rec_1657175,Human_Splice_Rec_1657278 Human_miRNA_ID_2257981 RMVar_hsa_circ_95827,RMVar_hsa_circ_269155,RMVar_hsa_circ_50940,RMVar_hsa_circ_175446 72637 RMVar_ID_72637 Human_SNP_ID_590689682 m1A Human chr16 - 791997 791997 791997 ACACCCGGTTTCAGGTCCGCCACCAGAACTCAAACACGTCAGGACAGAAGGCGAGCCAGAGACGG ACACCCGGTTTCAGGTCCGCCACCAGAACTCACACACGTCAGGACAGAAGGCGAGCCAGAGACGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:791961..792413 26863196 MeRIP-seq:(Medium) rs1218418111 Functional Loss SNV dbSNP153 33..33 33 - - - 72638 RMVar_ID_72638 Human_SNP_ID_590689876 m1A Human chr16 - 792349 792349 792349 GCCCACCCACCTACCCAGGCATCAAGGAGCCCACCACGGGGGCCCCGTCGATCTCATCGATGACC GCCCACCCACCTACCCAGGCATCAAGGAGCCCCCCACGGGGGCCCCGTCGATCTCATCGATGACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:792332..792448 26863196 MeRIP-seq:(Medium) rs1369014193 Functional Loss SNV dbSNP153 33..33 33 - - - 72639 RMVar_ID_72639 Human_SNP_ID_590690993 m1A Human chr16 - 794087 794087 794087 CCCGCGTCCCCGTCACCCAGCAGGAGTGTGTCAGCAGGCAGGGCGGGGTCCTGGCCCACACGGCG CCCGCGTCCCCGTCACCCAGCAGGAGTGTGTCGGCAGGCAGGGCGGGGTCCTGGCCCACACGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:794064..794129 26863196 MeRIP-seq:(Medium) rs754914897 Functional Loss SNV dbSNP153 33..33 33 - - - 72640 RMVar_ID_72640 Human_SNP_ID_590691120 m1A Human chr16 - 794325 794325 794325 CCTCAGAGACTTCCTGGCACCCCATTTCCCGAACCTGCCTCTCTCAGCACCCCCAAAGCGCCTCC CCTCAGAGACTTCCTGGCACCCCATTTCCCGACCCTGCCTCTCTCAGCACCCCCAAAGCGCCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:794323..794548 26863196 MeRIP-seq:(Medium) rs1203662847 Functional Loss SNV dbSNP153 33..33 33 - - - 72641 RMVar_ID_72641 Human_SNP_ID_590691304 m1A Human chr16 + 794732 794732 794732 AGCGTGGAGCAGCGGCGGGGATAGACTCCCCCACGGAACAGGGGTGGGGACGCCACGGCCTGGAC AGCGTGGAGCAGCGGCGGGGATAGACTCCCCCCCGGAACAGGGGTGGGGACGCCACGGCCTGGAC A C CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:794729..794823 26863196 MeRIP-seq:(Medium) rs1398533900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269155 72642 RMVar_ID_72642 Human_SNP_ID_590691381 m1A Human chr16 + 794880 794880 794880 GGTCACCCCCTCGTGTCAGTCTCTGTCAAGTCAGTCTCTGTCAAGCTGTAGCGAGGATGCTCAGG GGTCACCCCCTCGTGTCAGTCTCTGTCAAGTCGGTCTCTGTCAAGCTGTAGCGAGGATGCTCAGG A G CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:794875..794964 26863196 MeRIP-seq:(Medium) rs1260020647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12829002 RMVar_hsa_circ_269155 72643 RMVar_ID_72643 Human_SNP_ID_590691609 m1A Human chr16 - 795280 795280 795280 AAGCAAACAGCACATGGAAGGCCACGGGCAGGAAGGGTGGGTAGCGCAGCAGCTGGAAGCTCTGG AAGCAAACAGCACATGGAAGGCCACGGGCAGGGAGGGTGGGTAGCGCAGCAGCTGGAAGCTCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:795230..795384 26863196 MeRIP-seq:(Medium) rs1476787726 Functional Loss SNV dbSNP153 33..33 33 - - - 72644 RMVar_ID_72644 Human_SNP_ID_590692809 m1A Human chr16 - 797055 797055 797055 CCTCCCGGGCCGCTCGCCTCATGATGTGCTCCAGCCGCTGCTCATGGTTGCGTGGGGCAGGTCGG CCTCCCGGGCCGCTCGCCTCATGATGTGCTCCGGCCGCTGCTCATGGTTGCGTGGGGCAGGTCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:797006..797123 26863196 MeRIP-seq:(Medium) rs765118548 Functional Loss SNV dbSNP153 33..33 33 - - - 72645 RMVar_ID_72645 Human_SNP_ID_590693103 m1A Human chr16 - 797658 797658 797658 ATGGGAGGAAGGACTAGTCAGTCGTATAGGACAGATGCCCCATCCAGCCCCTACCCAAGACAGGA ATGGGAGGAAGGACTAGTCAGTCGTATAGGACCGATGCCCCATCCAGCCCCTACCCAAGACAGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:797655..797962 26863196 MeRIP-seq:(Medium) rs1385321214 Functional Loss SNV dbSNP153 33..33 33 - - - 72646 RMVar_ID_72646 Human_SNP_ID_590693189 m1A Human chr16 - 797770 797768 797771 CCCCCCACAACCCCCAGGCCCCCCACAACCCCACAACACCCCCACACACACCTGCACTCGGGACT CCCCCCACAACCCCCAGGCCCCCCACAACCC___AACACCCCCACACACACCTGCACTCGGGACT TGTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:797767..797857 26863196 MeRIP-seq:(Medium) rs777752861 Functional Loss DEL dbSNP153 32..34 33 - - - 72647 RMVar_ID_72647 Human_SNP_ID_590693190 m1A Human chr16 - 797770 797770 797770 CCCCCCACAACCCCCAGGCCCCCCACAACCCCACAACACCCCCACACACACCTGCACTCGGGACT CCCCCCACAACCCCCAGGCCCCCCACAACCCCCCAACACCCCCACACACACCTGCACTCGGGACT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:797767..797857 26863196 MeRIP-seq:(Medium) rs761231933 Functional Loss SNV dbSNP153 33..33 33 - - - 72648 RMVar_ID_72648 Human_SNP_ID_590693356 m1A Human chr16 + 797993 797993 797993 AGGGACTTGCTCTAGTTCTCTGAGCCGCGGACATGCCCTCGCATTGCTTCCCGCAGAGTGCAGAG AGGGACTTGCTCTAGTTCTCTGAGCCGCGGACGTGCCCTCGCATTGCTTCCCGCAGAGTGCAGAG A G CHTF18 Ensembl:ENSG00000127586 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:797943..798752 26863196 MeRIP-seq:(Medium) rs749848369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480790,Human_RBP_ID_891089,Human_RBP_ID_1005753,Human_RBP_ID_1523640,Human_RBP_ID_4386879,Human_RBP_ID_8440476,Human_RBP_ID_18162847,Human_RBP_ID_18685669 Human_miRNA_ID_1373028 72649 RMVar_ID_72649 Human_SNP_ID_590693465 m1A Human chr16 + 798133 798132 798134 AGGATGGTGGGAGTGGGGCCGGGCGTGGGCTCATAGGATGGTGTGAGTGGGGCCAGGAGTGGGGC AGGATGGTGGGAGTGGGGCCGGGCGTGGGCTC__AGGATGGTGTGAGTGGGGCCAGGAGTGGGGC CAT C CHTF18 Ensembl:ENSG00000127586 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:798082..798737 26863196 MeRIP-seq:(Medium) rs1323656988 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_261272,Human_RBP_ID_8086603,Human_RBP_ID_8184009,Human_RBP_ID_9419559,Human_RBP_ID_22581598,Human_RBP_ID_22943034 72650 RMVar_ID_72650 Human_SNP_ID_590693578 m1A Human chr16 + 798330 798330 798330 GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGAGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGCGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG A C CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:798079..798726 26863196 MeRIP-seq:(Medium) rs1464962445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802423 72651 RMVar_ID_72651 Human_SNP_ID_590693579 m1A Human chr16 + 798330 798330 798330 GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGAGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGGGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG A G CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:798079..798726 26863196 MeRIP-seq:(Medium) rs1464962445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802423 72652 RMVar_ID_72652 Human_SNP_ID_590693580 m1A Human chr16 + 798330 798330 798330 GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGAGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG GGGGCTCACAGGTTGGTGTGAGTGGGGCTGGGTGTGGGGCTCACAGGATGGAGTGAGTGGGGCCG A T CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:798079..798726 26863196 MeRIP-seq:(Medium) rs1464962445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802423 72653 RMVar_ID_72653 Human_SNP_ID_590694025 m1A Human chr16 + 799151 799151 799151 GCACAGGAGGAAGCCACAGGGCCGAGGCCACCAGCCTGTAGTCCCCACCCCCGCTGCTCCCCGCA GCACAGGAGGAAGCCACAGGGCCGAGGCCACCCGCCTGTAGTCCCCACCCCCGCTGCTCCCCGCA A C CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:799116..799201 26863196 MeRIP-seq:(Medium) rs1206954989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503884,Human_RBP_ID_22206337,Human_RBP_ID_22943043 72654 RMVar_ID_72654 Human_SNP_ID_590695776 m1A Human chr16 + 803728 803724 803728 GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGACCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG GGCTGTCCTAGGGGGACCCTGTGGCCTGGAGGCCCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG CAGGA GAGGC - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs386787599 Functional Loss MNV dbSNP153 29..33 33 - - - 72655 RMVar_ID_72655 Human_SNP_ID_590695781 m1A Human chr16 + 803728 803728 803728 GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGACCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGCCCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11248950 Functional Loss SNV dbSNP153 33..33 33 - - - 72656 RMVar_ID_72656 Human_SNP_ID_590695782 m1A Human chr16 + 803728 803728 803728 GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGACCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGGCCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11248950 Functional Loss SNV dbSNP153 33..33 33 - - - 72657 RMVar_ID_72657 Human_SNP_ID_590697324 m1A Human chr16 - 807458 807458 807458 GAGGCGGCGGCGAGGGGCCCTGGCGAGGGCACAGGCGGGTCAGGGAGCAGCGCTGGCTGAGGCCC GAGGCGGCGGCGAGGGGCCCTGGCGAGGGCACGGGCGGGTCAGGGAGCAGCGCTGGCTGAGGCCC T C lnc-GNG13-6,lnc-GNG13-6:2,lnc-GNG13-6:3 RNACentral:URS0000D5BE89,RNACentral:URS0000D5DC2B,RNACentral:URS0000D5862B lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:807308..807564 26863196 MeRIP-seq:(Medium) rs1217510832 Functional Loss SNV dbSNP153 33..33 33 - - - 72658 RMVar_ID_72658 Human_SNP_ID_590717054 m1A Human chr16 + 857822 857799 857822 ATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT ATGGGTGTGC_______________________GTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT CGTGGTGTCTCGGGATGGGTGTGA C AL023882.1 Ensembl:ENSG00000287855 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:857815..857904 26863196 MeRIP-seq:(Medium) rs1567132922 Functional Loss DEL dbSNP153 11..33 33 - - - 72659 RMVar_ID_72659 Human_SNP_ID_590717066 m1A Human chr16 + 857822 857822 857822 ATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT ATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT A C AL023882.1 Ensembl:ENSG00000287855 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:857815..857904 26863196 MeRIP-seq:(Medium) rs373550963 Functional Loss SNV dbSNP153 33..33 33 - - - 72660 RMVar_ID_72660 Human_SNP_ID_590717067 m1A Human chr16 + 857822 857822 857822 ATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT ATGGGTGTGCGTGGTGTCTCGGGATGGGTGTGGGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCT A G AL023882.1 Ensembl:ENSG00000287855 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:857815..857904 26863196 MeRIP-seq:(Medium) rs373550963 Functional Loss SNV dbSNP153 33..33 33 - - - 72661 RMVar_ID_72661 Human_SNP_ID_590718301 m1A Human chr16 + 859847 859843 859848 AGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCACGGGATGGGTGTGCAGTGGTGTCTCGGGATGG AGTGGTGTCTCGGGATGGGTGTGAGTGGT_____GGGATGGGTGTGCAGTGGTGTCTCGGGATGG TGTCAC T AL023882.1 Ensembl:ENSG00000287855 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:859840..859967 26863196 MeRIP-seq:(Medium) rs1176622966 Functional Loss DEL dbSNP153 30..34 33 - - - 72662 RMVar_ID_72662 Human_SNP_ID_590718302 m1A Human chr16 + 859847 859847 859847 AGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCACGGGATGGGTGTGCAGTGGTGTCTCGGGATGG AGTGGTGTCTCGGGATGGGTGTGAGTGGTGTCTCGGGATGGGTGTGCAGTGGTGTCTCGGGATGG A T AL023882.1 Ensembl:ENSG00000287855 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:859840..859967 26863196 MeRIP-seq:(Medium) rs375538976 Functional Loss SNV dbSNP153 33..33 33 - - - 72663 RMVar_ID_72663 Human_SNP_ID_590731439 m1A Human chr16 - 894272 894272 894272 CAGGGGATGGGTGGGCGCACTGCCAGGTGGACAGGGGGACAGGTGGGCGGACGGTCCAGTGGACA CAGGGGATGGGTGGGCGCACTGCCAGGTGGACGGGGGGACAGGTGGGCGGACGGTCCAGTGGACA T C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:894267..894342 26863196 MeRIP-seq:(Medium) rs1199909182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8184023 RMVar_hsa_circ_76977,RMVar_hsa_circ_175447,RMVar_hsa_circ_373756,RMVar_hsa_circ_79235,RMVar_hsa_circ_175448,RMVar_hsa_circ_175449,RMVar_hsa_circ_297793,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_81824,RMVar_hsa_circ_314466,RMVar_hsa_circ_175456 72664 RMVar_ID_72664 Human_SNP_ID_590731461 m1A Human chr16 - 894317 894313 894317 ACGGTCCGGTGGACAGGGGGACGGGTGGGTGGACGATCCGGTGGACAGGGGATGGGTGGGCGCAC ACGGTCCGGTGGACAGGGGGACGGGTGGGTGG____TCCGGTGGACAGGGGATGGGTGGGCGCAC ATCGT A LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:894314..894397 26863196 MeRIP-seq:(Medium) rs1567197720 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8184023 RMVar_hsa_circ_76977,RMVar_hsa_circ_175447,RMVar_hsa_circ_373756,RMVar_hsa_circ_79235,RMVar_hsa_circ_175448,RMVar_hsa_circ_175449,RMVar_hsa_circ_297793,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_81824,RMVar_hsa_circ_314466,RMVar_hsa_circ_175456 72665 RMVar_ID_72665 Human_SNP_ID_590738302 m1A Human chr16 - 914509 914505 914509 GGAGGGAGGGAGTGTGTCACCAATGGTCATGGAAGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT GGAGGGAGGGAGTGTGTCACCAATGGTCATGG____GAGGGAGGGAGCGTGTCTGGTTTTGCACT CCCTT C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:914504..914681 26863196 MeRIP-seq:(Medium) rs1279944828 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3502286,Human_RBP_ID_8086606,Human_RBP_ID_8184027 RMVar_hsa_circ_78016,RMVar_hsa_circ_79235,RMVar_hsa_circ_175449,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175455,RMVar_hsa_circ_314466,RMVar_hsa_circ_292483,RMVar_hsa_circ_117346,RMVar_hsa_circ_175458,RMVar_hsa_circ_175459,RMVar_hsa_circ_175457 72666 RMVar_ID_72666 Human_SNP_ID_590738304 m1A Human chr16 - 914509 914506 914509 GGAGGGAGGGAGTGTGTCACCAATGGTCATGGAAGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT GGAGGGAGGGAGTGTGTCACCAATGGTCATGG___GGAGGGAGGGAGCGTGTCTGGTTTTGCACT CCTT C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:914504..914681 26863196 MeRIP-seq:(Medium) rs1451337257 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3502286,Human_RBP_ID_8086606,Human_RBP_ID_8184027 RMVar_hsa_circ_78016,RMVar_hsa_circ_79235,RMVar_hsa_circ_175449,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175455,RMVar_hsa_circ_314466,RMVar_hsa_circ_292483,RMVar_hsa_circ_117346,RMVar_hsa_circ_175458,RMVar_hsa_circ_175459,RMVar_hsa_circ_175457 72667 RMVar_ID_72667 Human_SNP_ID_590738307 m1A Human chr16 - 914509 914508 914510 GGAGGGAGGGAGTGTGTCACCAATGGTCATGGAAGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT GGAGGGAGGGAGTGTGTCACCAATGGTCATG__AGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT TTC T LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:914504..914681 26863196 MeRIP-seq:(Medium) rs1491361754 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3502286,Human_RBP_ID_8086606,Human_RBP_ID_8184027 RMVar_hsa_circ_78016,RMVar_hsa_circ_79235,RMVar_hsa_circ_175449,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175455,RMVar_hsa_circ_314466,RMVar_hsa_circ_292483,RMVar_hsa_circ_117346,RMVar_hsa_circ_175458,RMVar_hsa_circ_175459,RMVar_hsa_circ_175457 72668 RMVar_ID_72668 Human_SNP_ID_590738309 m1A Human chr16 - 914509 914509 914509 GGAGGGAGGGAGTGTGTCACCAATGGTCATGGAAGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT GGAGGGAGGGAGTGTGTCACCAATGGTCATGGGAGGGAGGGAGGGAGCGTGTCTGGTTTTGCACT T C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:914504..914681 26863196 MeRIP-seq:(Medium) rs1205441899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502286,Human_RBP_ID_8086606,Human_RBP_ID_8184027 RMVar_hsa_circ_78016,RMVar_hsa_circ_79235,RMVar_hsa_circ_175449,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175455,RMVar_hsa_circ_314466,RMVar_hsa_circ_292483,RMVar_hsa_circ_117346,RMVar_hsa_circ_175458,RMVar_hsa_circ_175459,RMVar_hsa_circ_175457 72669 RMVar_ID_72669 Human_SNP_ID_590752094 m1A Human chr16 + 953113 953072 953113 CCAGCCTCCTACACGTCCACACAGACACCCCAAACCAGCCTCCTACATATCCACACAGACACCCA _________________________________ACCAGCCTCCTACATATCCACACAGACACCCA CACTCCAAACCAGCCTCCTACACGTCCACACAGACACCCCAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:953085..953182 26863196 MeRIP-seq:(Medium) rs1178319905 Functional Loss DEL dbSNP153 1..33 33 - - - 72670 RMVar_ID_72670 Human_SNP_ID_590752122 m1A Human chr16 + 953113 953113 953113 CCAGCCTCCTACACGTCCACACAGACACCCCAAACCAGCCTCCTACATATCCACACAGACACCCA CCAGCCTCCTACACGTCCACACAGACACCCCACACCAGCCTCCTACATATCCACACAGACACCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:953085..953182 26863196 MeRIP-seq:(Medium) rs1376272956 Functional Loss SNV dbSNP153 33..33 33 - - - 72671 RMVar_ID_72671 Human_SNP_ID_590753975 m1A Human chr16 + 955906 955906 955906 GCCTATAGGTGAGCCACACTTGCCCTCTACGCAGACCACAGGTCTCCGAGTTCACGTCTCACGGC GCCTATAGGTGAGCCACACTTGCCCTCTACGCCGACCACAGGTCTCCGAGTTCACGTCTCACGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:955904..955992 26863196 MeRIP-seq:(Medium) rs1044464636 Functional Loss SNV dbSNP153 33..33 33 - - - 72672 RMVar_ID_72672 Human_SNP_ID_590754097 m1A Human chr16 - 956184 956184 956184 GACGTGAACTCGGAGACCTGTGGATGTGAGAGAGCCGTCGTGGGGTGGGCGCCGTGAGACATGAA GACGTGAACTCGGAGACCTGTGGATGTGAGAGCGCCGTCGTGGGGTGGGCGCCGTGAGACATGAA T G LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:956179..956244 26863196 MeRIP-seq:(Medium) rs371511940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78016,RMVar_hsa_circ_175450,RMVar_hsa_circ_99820,RMVar_hsa_circ_175459 72673 RMVar_ID_72673 Human_SNP_ID_590762722 m1A Human chr16 + 981337 981337 981337 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGT A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:981329..981411 26863410 MeRIP-seq:(Medium) rs1203547040 Functional Loss SNV dbSNP153 33..33 33 - - - 72674 RMVar_ID_72674 Human_SNP_ID_590764433 m1A Human chr16 - 984982 984982 984982 CGACGGGGCACTCTTGTGGGCCCACACGGGGGACGCCCCGGCGTGGAAGTAGGCGCCCCCATAGG CGACGGGGCACTCTTGTGGGCCCACACGGGGGTCGCCCCGGCGTGGAAGTAGGCGCCCCCATAGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:984937..985087 32194978 MeRIP-seq:(Medium) rs372363740 Functional Loss SNV dbSNP153 33..33 33 - - - 72675 RMVar_ID_72675 Human_SNP_ID_590825222 m1A Human chr16 + 1153369 1153369 1153369 GCGCTGGGGGCCGGGGCCGGGGCCGGGGGCGGAGGCGCTGGGGGCCGGGGCCGGGGCCGGGCGCC GCGCTGGGGGCCGGGGCCGGGGCCGGGGGCGGGGGCGCTGGGGGCCGGGGCCGGGGCCGGGCGCC A G CACNA1H Ensembl:ENSG00000196557 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1153146..1154018 26863196 MeRIP-seq:(Medium) rs1317609544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26779969 RMVar_hsa_circ_97004,RMVar_hsa_circ_175463 72676 RMVar_ID_72676 Human_SNP_ID_590827495 m1A Human chr16 - 1157879 1157877 1157879 GGCCGTGGGTCGGGCGCAACGGCCGAGTTCACACCCTGGTCCACCCAGGCAGAAGGGACGGGACG GGCCGTGGGTCGGGCGCAACGGCCGAGTTCAC__CCTGGTCCACCCAGGCAGAAGGGACGGGACG GGT G AC120498.3 Ensembl:ENSG00000260403 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1157875..1157974 32194978 MeRIP-seq:(Medium) rs1341905375 Functional Loss DEL dbSNP153 33..34 33 - - - 72677 RMVar_ID_72677 Human_SNP_ID_590833576 m1A Human chr16 - 1171930 1171930 1171930 AGCGTCCGTCCTGGCGCCCGCCTGGCCTGTGAACATGCCCCCACCCGTGGACACTGCTCCCTGGC AGCGTCCGTCCTGGCGCCCGCCTGGCCTGTGAGCATGCCCCCACCCGTGGACACTGCTCCCTGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1171928..1172044 32194978 MeRIP-seq:(Medium) rs554401715 Functional Loss SNV dbSNP153 33..33 33 - - - 72678 RMVar_ID_72678 Human_SNP_ID_590839526 m1A Human chr16 - 1185692 1185692 1185692 CTCCGGCCCCTACGCACGCCGACCGTCTACTCACCCGCCCCGTACACACCCCGCCTCCGGCCCCT CTCCGGCCCCTACGCACGCCGACCGTCTACTCGCCCGCCCCGTACACACCCCGCCTCCGGCCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr16:1185564..1185822;chr16:1185610..1185745 26863196 MeRIP-seq:(Medium) rs1280663812 Functional Loss SNV dbSNP153 33..33 33 - - - 72679 RMVar_ID_72679 Human_SNP_ID_590839527 m1A Human chr16 - 1185692 1185692 1185692 CTCCGGCCCCTACGCACGCCGACCGTCTACTCACCCGCCCCGTACACACCCCGCCTCCGGCCCCT CTCCGGCCCCTACGCACGCCGACCGTCTACTCCCCCGCCCCGTACACACCCCGCCTCCGGCCCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr16:1185564..1185822;chr16:1185610..1185745 26863196 MeRIP-seq:(Medium) rs1280663812 Functional Loss SNV dbSNP153 33..33 33 - - - 72680 RMVar_ID_72680 Human_SNP_ID_590839684 m1A Human chr16 - 1185961 1185957 1185961 CCCCGTACACACCCCGCCTCCGGCCCCTACGCACGCCGTCTACTCACCCGCCCCGTACACACCCC CCCCGTACACACCCCGCCTCCGGCCCCTACGC____CGTCTACTCACCCGCCCCGTACACACCCC GGCGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1185930..1186079 26863196 MeRIP-seq:(Medium) rs1287639545 Functional Loss DEL dbSNP153 33..36 33 - - - 72681 RMVar_ID_72681 Human_SNP_ID_590840590 m1A Human chr16 - 1187827 1187827 1187827 CTGTGTGCCCCTCCTCAAGAGATAGTTAAGGCATCAAAGCCACAGGCCAGCCTCAGCTCCTCAGA CTGTGTGCCCCTCCTCAAGAGATAGTTAAGGCGTCAAAGCCACAGGCCAGCCTCAGCTCCTCAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1187820..1187954 32194978 MeRIP-seq:(Medium) rs1258066965 Functional Loss SNV dbSNP153 33..33 33 - - - 72682 RMVar_ID_72682 Human_SNP_ID_590840591 m1A Human chr16 - 1187827 1187827 1187827 CTGTGTGCCCCTCCTCAAGAGATAGTTAAGGCATCAAAGCCACAGGCCAGCCTCAGCTCCTCAGA CTGTGTGCCCCTCCTCAAGAGATAGTTAAGGCCTCAAAGCCACAGGCCAGCCTCAGCTCCTCAGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1187820..1187954 32194978 MeRIP-seq:(Medium) rs1258066965 Functional Loss SNV dbSNP153 33..33 33 - - - 72683 RMVar_ID_72683 Human_SNP_ID_590848099 m1A Human chr16 + 1202251 1202251 1202251 GGGTGGCACATGCCGCAGCCACTGCCGCTGCCAGCCTCAGACTGGCCACAGGGCTGGGCACCATG GGGTGGCACATGCCGCAGCCACTGCCGCTGCCCGCCTCAGACTGGCCACAGGGCTGGGCACCATG A C CACNA1H Ensembl:ENSG00000196557 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1202154..1202344 32194978 MeRIP-seq:(Medium) rs752670365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27559837 RMVar_hsa_circ_97004,RMVar_hsa_circ_86217,RMVar_hsa_circ_79902,RMVar_hsa_circ_175463,RMVar_hsa_circ_175464,RMVar_hsa_circ_100184,RMVar_hsa_circ_105479,RMVar_hsa_circ_175465,RMVar_hsa_circ_95814,RMVar_hsa_circ_175466,RMVar_hsa_circ_175467,RMVar_hsa_circ_175468 72684 RMVar_ID_72684 Human_SNP_ID_590857412 m1A Human chr16 + 1218402 1218402 1218402 AGGCACGGGAGGATGCGGAGCTGGACGCCGAGATCGAGCTGGAGATGGCGCAGGGCCCCGGGAGT AGGCACGGGAGGATGCGGAGCTGGACGCCGAGGTCGAGCTGGAGATGGCGCAGGGCCCCGGGAGT A G CACNA1H Ensembl:ENSG00000196557 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1218351..1218465 26863196 MeRIP-seq:(Medium) rs369689966 Functional Loss SNV dbSNP153 33..33 33 - - - 72685 RMVar_ID_72685 Human_SNP_ID_590858443 m1A Human chr16 - 1220257 1220242 1220257 GCCATGGGGCTCGGCTGTGGGCTGCCAGGGGCAGGCGGAGCTGGTGATGTGGCTGACCTCCTCGT GCCATGGGGCTCGGCTGTGGGCTGCCAGGGGC_______________TGTGGCTGACCTCCTCGT ATCACCAGCTCCGCCT A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1220164..1220321 26863410 MeRIP-seq:(Medium) rs774660673 Functional Loss DEL dbSNP153 33..47 33 - - - Clinvar_Rec_308 72686 RMVar_ID_72686 Human_SNP_ID_590858576 m1A Human chr16 + 1220423 1220423 1220423 GTGGCGGCCCTCGGCGGAGCTGGGCAGCGGGGAGCCTGGGGAGGCGAAGGCCTGGGGCCCTGAGG GTGGCGGCCCTCGGCGGAGCTGGGCAGCGGGGCGCCTGGGGAGGCGAAGGCCTGGGGCCCTGAGG A C CACNA1H Ensembl:ENSG00000196557 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1220378..1220479 26863196 MeRIP-seq:(Medium) rs749459112 Functional Loss SNV dbSNP153 33..33 33 - - - 72687 RMVar_ID_72687 Human_SNP_ID_590858585 m1A Human chr16 + 1220432 1220432 1220432 CTCGGCGGAGCTGGGCAGCGGGGAGCCTGGGGAGGCGAAGGCCTGGGGCCCTGAGGCCGAGCCCG CTCGGCGGAGCTGGGCAGCGGGGAGCCTGGGGGGGCGAAGGCCTGGGGCCCTGAGGCCGAGCCCG A G CACNA1H Ensembl:ENSG00000196557 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1220382..1220496 32194978 MeRIP-seq:(Medium) rs574490640 Functional Loss SNV dbSNP153 33..33 33 - - - 72688 RMVar_ID_72688 Human_SNP_ID_590858586 m1A Human chr16 + 1220432 1220432 1220432 CTCGGCGGAGCTGGGCAGCGGGGAGCCTGGGGAGGCGAAGGCCTGGGGCCCTGAGGCCGAGCCCG CTCGGCGGAGCTGGGCAGCGGGGAGCCTGGGGTGGCGAAGGCCTGGGGCCCTGAGGCCGAGCCCG A T CACNA1H Ensembl:ENSG00000196557 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1220382..1220496 32194978 MeRIP-seq:(Medium) rs574490640 Functional Loss SNV dbSNP153 33..33 33 - - - 72689 RMVar_ID_72689 Human_SNP_ID_590892786 m1A Human chr16 - 1309725 1309725 1309725 CCCGGCGAGCGTAGCGGACAGGTGGAGGACCGAGCGGGGCGGCGGCGGCGGCGCTTCCCTTTGTC CCCGGCGAGCGTAGCGGACAGGTGGAGGACCGGGCGGGGCGGCGGCGGCGGCGCTTCCCTTTGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:1309626..1309819;chr16:1309626..1309813 26863196 MeRIP-seq:(Medium) rs1379558891 Functional Loss SNV dbSNP153 33..33 33 - - - 72690 RMVar_ID_72690 Human_SNP_ID_590894442 m1A Human chr16 + 1314072 1314072 1314072 ATCGCCCTCAGCAGACTCGCCCAGGAGAGGAAAGCATGGAGGAAAGACCACCCATTTGTAAGGAG ATCGCCCTCAGCAGACTCGCCCAGGAGAGGAAGGCATGGAGGAAAGACCACCCATTTGTAAGGAG A G UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1314001..1314100 26863196 MeRIP-seq:(Medium) rs768789039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817733,Human_RBP_ID_889249,Human_RBP_ID_1512455,Human_RBP_ID_1838133,Human_RBP_ID_3491360,Human_RBP_ID_4350708,Human_RBP_ID_19070394,Human_RBP_ID_23678805,Human_RBP_ID_26328025,Human_RBP_ID_26810836 Human_Splice_Rec_1658212,Human_Splice_Rec_1658213,Human_Splice_Rec_1658224,Human_Splice_Rec_1658225,Human_Splice_Rec_1658238,Human_Splice_Rec_1658239,Human_Splice_Rec_1658250,Human_Splice_Rec_1658251,Human_Splice_Rec_1658256,Human_Splice_Rec_1658257,Human_Splice_Rec_1658280,Human_Splice_Rec_1658281,Human_Splice_Rec_1658286,Human_Splice_Rec_1658287,Human_Splice_Rec_1658298,Human_Splice_Rec_1658299,Human_Splice_Rec_1658304,Human_Splice_Rec_1658305,Human_Splice_Rec_1658308,Human_Splice_Rec_1658309,Human_Splice_Rec_1658320,Human_Splice_Rec_1658321,Human_Splice_Rec_1658332,Human_Splice_Rec_1658333,Human_Splice_Rec_1658341,Human_Splice_Rec_1658349 Human_miRNA_ID_2897026,Human_miRNA_ID_2897027 RMVar_hsa_circ_97309,RMVar_hsa_circ_319499,RMVar_hsa_circ_337966,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_175475,RMVar_hsa_circ_25213,RMVar_hsa_circ_175474,RMVar_hsa_circ_175472 72691 RMVar_ID_72691 Human_SNP_ID_590894445 m1A Human chr16 + 1314075 1314075 1314075 GCCCTCAGCAGACTCGCCCAGGAGAGGAAAGCATGGAGGAAAGACCACCCATTTGTAAGGAGGGC GCCCTCAGCAGACTCGCCCAGGAGAGGAAAGCGTGGAGGAAAGACCACCCATTTGTAAGGAGGGC A G UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1314001..1314075 26863196 MeRIP-seq:(Medium) rs762154179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889249,Human_RBP_ID_1512455,Human_RBP_ID_1838133,Human_RBP_ID_3491360,Human_RBP_ID_4350708,Human_RBP_ID_19070394,Human_RBP_ID_23678805,Human_RBP_ID_26328025,Human_RBP_ID_26810836 Human_Splice_Rec_1658212,Human_Splice_Rec_1658213,Human_Splice_Rec_1658224,Human_Splice_Rec_1658225,Human_Splice_Rec_1658238,Human_Splice_Rec_1658239,Human_Splice_Rec_1658250,Human_Splice_Rec_1658251,Human_Splice_Rec_1658256,Human_Splice_Rec_1658257,Human_Splice_Rec_1658280,Human_Splice_Rec_1658281,Human_Splice_Rec_1658286,Human_Splice_Rec_1658287,Human_Splice_Rec_1658298,Human_Splice_Rec_1658299,Human_Splice_Rec_1658304,Human_Splice_Rec_1658305,Human_Splice_Rec_1658308,Human_Splice_Rec_1658309,Human_Splice_Rec_1658320,Human_Splice_Rec_1658321,Human_Splice_Rec_1658332,Human_Splice_Rec_1658333,Human_Splice_Rec_1658341,Human_Splice_Rec_1658349 Human_miRNA_ID_2897026,Human_miRNA_ID_2897027 RMVar_hsa_circ_97309,RMVar_hsa_circ_319499,RMVar_hsa_circ_337966,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_175475,RMVar_hsa_circ_25213,RMVar_hsa_circ_175474,RMVar_hsa_circ_175472 72692 RMVar_ID_72692 Human_SNP_ID_590894579 m1A Human chr16 + 1314364 1314364 1314364 ATGAACCTCATGAACTGGGAGTGCGCCATTCCAGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT ATGAACCTCATGAACTGGGAGTGCGCCATTCCGGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT A G UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1314253..1314414 26863196 MeRIP-seq:(Medium) rs4610 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_468382,Human_RBP_ID_1512459,Human_RBP_ID_8427778,Human_RBP_ID_12668039,Human_RBP_ID_19070395,Human_RBP_ID_26809801 Human_Splice_Rec_1658214,Human_Splice_Rec_1658215,Human_Splice_Rec_1658226,Human_Splice_Rec_1658227,Human_Splice_Rec_1658240,Human_Splice_Rec_1658241,Human_Splice_Rec_1658252,Human_Splice_Rec_1658253,Human_Splice_Rec_1658258,Human_Splice_Rec_1658259,Human_Splice_Rec_1658268,Human_Splice_Rec_1658269,Human_Splice_Rec_1658282,Human_Splice_Rec_1658288,Human_Splice_Rec_1658289,Human_Splice_Rec_1658306,Human_Splice_Rec_1658310,Human_Splice_Rec_1658311,Human_Splice_Rec_1658322,Human_Splice_Rec_1658323,Human_Splice_Rec_1658334,Human_Splice_Rec_1658335,Human_Splice_Rec_1658342,Human_Splice_Rec_1658343,Human_Splice_Rec_1658350,Human_Splice_Rec_1658351 GWAS_ID_8861 RMVar_hsa_circ_27192,RMVar_hsa_circ_319499,RMVar_hsa_circ_337966,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_25213,RMVar_hsa_circ_175474,RMVar_hsa_circ_175472,RMVar_hsa_circ_343464 72693 RMVar_ID_72693 Human_SNP_ID_590895111 m1A Human chr16 + 1315710 1315710 1315710 AAACTACGGATGCTTTTCAAAGATGATTATCCATCTTCGCCACCAAAATGTAAGTAGCTCCCTGT AAACTACGGATGCTTTTCAAAGATGATTATCCGTCTTCGCCACCAAAATGTAAGTAGCTCCCTGT A G UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1315651..1315725 26863196 MeRIP-seq:(Medium) rs369564528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468388,Human_RBP_ID_2468219,Human_RBP_ID_8804688,Human_RBP_ID_9372025,Human_RBP_ID_19072759,Human_RBP_ID_22196561,Human_RBP_ID_22441680,Human_RBP_ID_27656431 Human_Splice_Rec_1658216,Human_Splice_Rec_1658217,Human_Splice_Rec_1658228,Human_Splice_Rec_1658229,Human_Splice_Rec_1658242,Human_Splice_Rec_1658243,Human_Splice_Rec_1658254,Human_Splice_Rec_1658260,Human_Splice_Rec_1658261,Human_Splice_Rec_1658270,Human_Splice_Rec_1658271,Human_Splice_Rec_1658290,Human_Splice_Rec_1658291,Human_Splice_Rec_1658300,Human_Splice_Rec_1658301,Human_Splice_Rec_1658312,Human_Splice_Rec_1658313,Human_Splice_Rec_1658324,Human_Splice_Rec_1658325,Human_Splice_Rec_1658336,Human_Splice_Rec_1658337,Human_Splice_Rec_1658344,Human_Splice_Rec_1658345,Human_Splice_Rec_1658352,Human_Splice_Rec_1658353 RMVar_hsa_circ_27192,RMVar_hsa_circ_319499,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_25213,RMVar_hsa_circ_175472,RMVar_hsa_circ_343464,RMVar_hsa_circ_175476,RMVar_hsa_circ_280086 72694 RMVar_ID_72694 Human_SNP_ID_590896718 m1A Human chr16 + 1319859 1319859 1319859 AGTCTGGCCCAGCTGGAAAGGATGTGGGGGCCACAGGTTAAGTGGCCACCCTGGGGCCTGTGTTC AGTCTGGCCCAGCTGGAAAGGATGTGGGGGCCGCAGGTTAAGTGGCCACCCTGGGGCCTGTGTTC A G UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1319851..1319970 32194978 MeRIP-seq:(Medium) rs1023837815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512496 Human_Splice_Rec_1658355 RMVar_hsa_circ_27192,RMVar_hsa_circ_284495,RMVar_hsa_circ_25213,RMVar_hsa_circ_175472,RMVar_hsa_circ_343464,RMVar_hsa_circ_175476,RMVar_hsa_circ_280086 72695 RMVar_ID_72695 Human_SNP_ID_590896816 m1A Human chr16 - 1320152 1320152 1320152 TTCGAATTTACCTGGAGGAAGAGGAAGAAAGGAAGCACTTTTTGGAGGCAGGCACTGTCCCAGAG TTCGAATTTACCTGGAGGAAGAGGAAGAAAGGCAGCACTTTTTGGAGGCAGGCACTGTCCCAGAG T G AL031714.1 Ensembl:ENSG00000261505 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1320151..1320300 32194978 MeRIP-seq:(Medium) rs1342677480 Functional Loss SNV dbSNP153 33..33 33 - - - 72696 RMVar_ID_72696 Human_SNP_ID_590899320 m1A Human chr16 + 1325788 1325788 1325788 ATGGAGCTGCGCTGTGCATAGGGTGCCACCTCAGGTGTCTGTCCCTTGTGTCCTCAGGAGGCAGC ATGGAGCTGCGCTGTGCATAGGGTGCCACCTCGGGTGTCTGTCCCTTGTGTCCTCAGGAGGCAGC A G UBE2I Ensembl:ENSG00000103275 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28457180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468420 72697 RMVar_ID_72697 Human_SNP_ID_590909420 m1A Human chr16 + 1349529 1349529 1349529 CCCCCGTCCCTGCGTCTGCTCCTCTTCACAGCAGCTGCTGCTGGCTCCTCCGCGCTCGGCGCCAG CCCCCGTCCCTGCGTCTGCTCCTCTTCACAGCCGCTGCTGCTGGCTCCTCCGCGCTCGGCGCCAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1349310..1349625 26863196 MeRIP-seq:(Medium) rs773165987 Functional Loss SNV dbSNP153 33..33 33 - - - 72698 RMVar_ID_72698 Human_SNP_ID_590909597 m1A Human chr16 - 1349937 1349937 1349937 TTCCTCTCTCGGCTCAGATCCCTTCGATGTGGATTCAGGGAGAGAGTTTGGAAACCCCAACAGGC TTCCTCTCTCGGCTCAGATCCCTTCGATGTGGTTTCAGGGAGAGAGTTTGGAAACCCCAACAGGC T A TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1349876..1349975 26863196 MeRIP-seq:(Medium) rs1301651961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1002921,Human_RBP_ID_4350814 Human_Splice_Rec_1658912,Human_Splice_Rec_1658913 RMVar_hsa_circ_80342,RMVar_hsa_circ_175478 72699 RMVar_ID_72699 Human_SNP_ID_590909602 m1A Human chr16 - 1349943 1349943 1349943 GCCACTTTCCTCTCTCGGCTCAGATCCCTTCGATGTGGATTCAGGGAGAGAGTTTGGAAACCCCA GCCACTTTCCTCTCTCGGCTCAGATCCCTTCGGTGTGGATTCAGGGAGAGAGTTTGGAAACCCCA T C TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1349376..1351500 32194978 MeRIP-seq:(Medium) rs1330913975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1002921 Human_Splice_Rec_1658912,Human_Splice_Rec_1658913 RMVar_hsa_circ_80342,RMVar_hsa_circ_175478 72700 RMVar_ID_72700 Human_SNP_ID_590909755 m1A Human chr16 - 1350194 1350194 1350194 GACCTTGCTGTCATTTTGCTGCGGAAGTTTAAATGGGGCAAGGGCTTCTTGGACCTGAACCGCCA GACCTTGCTGTCATTTTGCTGCGGAAGTTTAAGTGGGGCAAGGGCTTCTTGGACCTGAACCGCCA T C TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1350043..1350200 26863196 MeRIP-seq:(Medium) rs375137026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468453,Human_RBP_ID_889253,Human_RBP_ID_1002923,Human_RBP_ID_1364944,Human_RBP_ID_1838167,Human_RBP_ID_6493935,Human_RBP_ID_8804700,Human_RBP_ID_9373565,Human_RBP_ID_17871814 Human_Splice_Rec_1658910,Human_Splice_Rec_1658918 Human_miRNA_ID_2002021,Human_miRNA_ID_2003405 RMVar_hsa_circ_84261,RMVar_hsa_circ_80342,RMVar_hsa_circ_101165,RMVar_hsa_circ_175478,RMVar_hsa_circ_175479,RMVar_hsa_circ_175480 72701 RMVar_ID_72701 Human_SNP_ID_590910274 m1A Human chr16 + 1351451 1351451 1351451 GCACCAGACCGCCGAATCTGTGGCCCAGGCGCAGGCAGCGCACCAGCCCCAGGCGGGCCAGCTTG GCACCAGACCGCCGAATCTGTGGCCCAGGCGCGGGCAGCGCACCAGCCCCAGGCGGGCCAGCTTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1351401..1351850 26863196 MeRIP-seq:(Medium) rs1293535538 Functional Loss SNV dbSNP153 33..33 33 - - - 72702 RMVar_ID_72702 Human_SNP_ID_590910411 m1A Human chr16 - 1351766 1351766 1351766 CGCAGGAGGGCAGCGCGCGGGCCGGGGGCGGAAGGCGGCCGCCCTCGGCACCTCCCGACGCGCTC CGCAGGAGGGCAGCGCGCGGGCCGGGGGCGGATGGCGGCCGCCCTCGGCACCTCCCGACGCGCTC T A TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:1351426..1351850 26863410 MeRIP-seq:(Medium) rs111834368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393437,Human_RBP_ID_9353085 Human_Splice_Rec_1658905 72703 RMVar_ID_72703 Human_SNP_ID_590910426 m1A Human chr16 - 1351787 1351787 1351787 CCCCAGGTCCGCGCCATGGGCCGCAGGAGGGCAGCGCGCGGGCCGGGGGCGGAAGGCGGCCGCCC CCCCAGGTCCGCGCCATGGGCCGCAGGAGGGCGGCGCGCGGGCCGGGGGCGGAAGGCGGCCGCCC T C TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:1351711..1351812 26863410 MeRIP-seq:(Medium) rs1004044382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392733,Human_RBP_ID_9353085 Human_Splice_Rec_1658905 72704 RMVar_ID_72704 Human_SNP_ID_590910430 m1A Human chr16 - 1351795 1351795 1351795 CCCCGGCACCCCAGGTCCGCGCCATGGGCCGCAGGAGGGCAGCGCGCGGGCCGGGGGCGGAAGGC CCCCGGCACCCCAGGTCCGCGCCATGGGCCGCTGGAGGGCAGCGCGCGGGCCGGGGGCGGAAGGC T A TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr16:1351376..1351850;chr16:1351607..1351800;chr16:1351369..1351875 26863196 MeRIP-seq:(Medium) rs1365465888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392733,Human_RBP_ID_9353085 72705 RMVar_ID_72705 Human_SNP_ID_590910432 m1A Human chr16 + 1351803 1351803 1351803 CCCCCGGCCCGCGCGCTGCCCTCCTGCGGCCCATGGCGCGGACCTGGGGTGCCGGGGACTCCCCA CCCCCGGCCCGCGCGCTGCCCTCCTGCGGCCCGTGGCGCGGACCTGGGGTGCCGGGGACTCCCCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1351375..1351850 26863196 MeRIP-seq:(Medium) rs1036898400 Functional Loss SNV dbSNP153 33..33 33 - - - 72706 RMVar_ID_72706 Human_SNP_ID_590910593 m1A Human chr16 - 1352023 1352023 1352023 GCGCGGGGCCTGGGGACGCGGACGGCCGGGCCACTCACCGCCGGCCGAGAGCCCGAGGAGCAACA GCGCGGGGCCTGGGGACGCGGACGGCCGGGCCGCTCACCGCCGGCCGAGAGCCCGAGGAGCAACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1352021..1352121 32194978 MeRIP-seq:(Medium) rs1394612898 Functional Loss SNV dbSNP153 33..33 33 - - - 72707 RMVar_ID_72707 Human_SNP_ID_590910767 m1A Human chr16 - 1352308 1352308 1352308 ACCCCCGCGCCGGCCAACAGCGCTCCTCACTCACCAGACACGGGTGAAGGATCCCTCTTGGCCTG ACCCCCGCGCCGGCCAACAGCGCTCCTCACTCGCCAGACACGGGTGAAGGATCCCTCTTGGCCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1352218..1352318 32194978 MeRIP-seq:(Medium) rs1555450744 Functional Loss SNV dbSNP153 33..33 33 - - - 72708 RMVar_ID_72708 Human_SNP_ID_590911759 m1A Human chr16 - 1355089 1355058 1355090 AGACCATCCACACCCGACCCCGCAGACGCGGGAGACCATCCACACCCGACCCCGCAGACGCGGCA AGACCATCCACACCCGACCCCGCAGACGCGG________________________________CA GCCGCGTCTGCGGGGTCGGGTGTGGATGGTCTC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1355082..1355310 26863196 MeRIP-seq:(Medium) rs1216336379 Functional Loss DEL dbSNP153 32..63 33 - - - 72709 RMVar_ID_72709 Human_SNP_ID_590911880 m1A Human chr16 + 1355291 1355289 1355292 TTCTGTCTTTGATGTAGCGCTCCTTCAACATCAACGTGTGAGGCGGATTGTGTGCAGTGGGTAGG TTCTGTCTTTGATGTAGCGCTCCTTCAACAT___CGTGTGAGGCGGATTGTGTGCAGTGGGTAGG TCAA T GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1354977..1355376 26863196 MeRIP-seq:(Medium) rs1357578143 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8086628,Human_RBP_ID_18481741,Human_RBP_ID_22697401 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 72710 RMVar_ID_72710 Human_SNP_ID_590912050 m1A Human chr16 - 1355831 1355831 1355831 CCCAGCCTGACCCCTGCAACTCACATGCTGGGAGCCGCACTTGCCATGGCTTCTCTAGCCAGGAT CCCAGCCTGACCCCTGCAACTCACATGCTGGGGGCCGCACTTGCCATGGCTTCTCTAGCCAGGAT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1355820..1355952 26863196 MeRIP-seq:(Medium) rs1391497746 Functional Loss SNV dbSNP153 33..33 33 - - - 72711 RMVar_ID_72711 Human_SNP_ID_590912468 m1A Human chr16 - 1356950 1356908 1356950 TCTGCCACTCAGACTCCTGCCCGCAGACCGCCACCCGCACACTCCCGCCCGCAGACCCCCGCCCG TCTGCCACTCAGACTCCTGCCCGCAGACCGCC_________________________________ CGAGAGTGTGCGGGCGGGGGTCTGCGGGCGGGAGTGTGCGGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1356938..1357209 26863196 MeRIP-seq:(Medium) rs1567181430 Functional Loss DEL dbSNP153 33..65 33 - - - 72712 RMVar_ID_72712 Human_SNP_ID_590912505 m1A Human chr16 - 1356950 1356950 1356950 TCTGCCACTCAGACTCCTGCCCGCAGACCGCCACCCGCACACTCCCGCCCGCAGACCCCCGCCCG TCTGCCACTCAGACTCCTGCCCGCAGACCGCCGCCCGCACACTCCCGCCCGCAGACCCCCGCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1356938..1357209 26863196 MeRIP-seq:(Medium) rs184886635 Functional Loss SNV dbSNP153 33..33 33 - - - 72713 RMVar_ID_72713 Human_SNP_ID_590912516 m1A Human chr16 + 1356965 1356965 1356965 GGGCGGGAGTGTGCGGGTGGCGGTCTGCGGGCAGGAGTCTGAGTGGCAGATGGGTGAGGGACACA GGGCGGGAGTGTGCGGGTGGCGGTCTGCGGGCGGGAGTCTGAGTGGCAGATGGGTGAGGGACACA A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1356934..1357179 26863196 MeRIP-seq:(Medium) rs1347523802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233222,Human_RBP_ID_261283,Human_RBP_ID_760633,Human_RBP_ID_815846,Human_RBP_ID_3502305,Human_RBP_ID_5087878,Human_RBP_ID_5316441,Human_RBP_ID_6494024,Human_RBP_ID_8084490,Human_RBP_ID_8184095,Human_RBP_ID_9419058,Human_RBP_ID_17206105,Human_RBP_ID_18481750,Human_RBP_ID_18938594,Human_RBP_ID_22370160,Human_RBP_ID_22415287,Human_RBP_ID_22712138,Human_RBP_ID_22739169,Human_RBP_ID_23274607,Human_RBP_ID_24414108,Human_RBP_ID_26779986 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 72714 RMVar_ID_72714 Human_SNP_ID_590915189 m1A Human chr16 + 1362897 1362895 1362898 GTTTGCTCACCCAGCACGGCATCCCCTACACGAGGCCCACAGGTGAGTCACCTGTGGGGAGAGGG GTTTGCTCACCCAGCACGGCATCCCCTACAC___GCCCACAGGTGAGTCACCTGTGGGGAGAGGG CGAG C GNPTG Ensembl:ENSG00000090581 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1362701..1362900 32194978 MeRIP-seq:(Medium) rs1555452112 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1658950,Human_Splice_Rec_1658951,Human_Splice_Rec_1658976,Human_Splice_Rec_1658996,Human_Splice_Rec_1658997,Human_Splice_Rec_1659014,Human_Splice_Rec_1659015 72715 RMVar_ID_72715 Human_SNP_ID_590915191 m1A Human chr16 + 1362897 1362897 1362897 GTTTGCTCACCCAGCACGGCATCCCCTACACGAGGCCCACAGGTGAGTCACCTGTGGGGAGAGGG GTTTGCTCACCCAGCACGGCATCCCCTACACGGGGCCCACAGGTGAGTCACCTGTGGGGAGAGGG A G GNPTG Ensembl:ENSG00000090581 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1362701..1362900 32194978 MeRIP-seq:(Medium) rs8062558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1658950,Human_Splice_Rec_1658951,Human_Splice_Rec_1658976,Human_Splice_Rec_1658996,Human_Splice_Rec_1658997,Human_Splice_Rec_1659014,Human_Splice_Rec_1659015 72716 RMVar_ID_72716 Human_SNP_ID_590915338 m1A Human chr16 - 1363089 1363089 1363089 CGCGTCCACCTCTGCTCTCCCACCACAAGGTCACAAACTCCCACGCAGTCCTGGGTCACCCCGCA CGCGTCCACCTCTGCTCTCCCACCACAAGGTCGCAAACTCCCACGCAGTCCTGGGTCACCCCGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1363041..1363250 26863196 MeRIP-seq:(Medium) rs1180995978 Functional Loss SNV dbSNP153 33..33 33 - - - 72717 RMVar_ID_72717 Human_SNP_ID_590915342 m1A Human chr16 - 1363094 1363094 1363094 TCGGCCGCGTCCACCTCTGCTCTCCCACCACAAGGTCACAAACTCCCACGCAGTCCTGGGTCACC TCGGCCGCGTCCACCTCTGCTCTCCCACCACAGGGTCACAAACTCCCACGCAGTCCTGGGTCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1363044..1363200 26863196 MeRIP-seq:(Medium) rs570294976 Functional Loss SNV dbSNP153 33..33 33 - - - 72718 RMVar_ID_72718 Human_SNP_ID_590915343 m1A Human chr16 - 1363094 1363094 1363094 TCGGCCGCGTCCACCTCTGCTCTCCCACCACAAGGTCACAAACTCCCACGCAGTCCTGGGTCACC TCGGCCGCGTCCACCTCTGCTCTCCCACCACACGGTCACAAACTCCCACGCAGTCCTGGGTCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1363044..1363200 26863196 MeRIP-seq:(Medium) rs570294976 Functional Loss SNV dbSNP153 33..33 33 - - - 72719 RMVar_ID_72719 Human_SNP_ID_590915355 m1A Human chr16 + 1363117 1363117 1363117 TTTGTGACCTTGTGGTGGGAGAGCAGAGGTGGACGCGGCCGAGAGCCCTACAGAGAAGCTGGCTG TTTGTGACCTTGTGGTGGGAGAGCAGAGGTGGTCGCGGCCGAGAGCCCTACAGAGAAGCTGGCTG A T GNPTG Ensembl:ENSG00000090581 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:1362976..1363250;chr16:1363001..1363225 26863196 MeRIP-seq:(Medium) rs1445812088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468478 72720 RMVar_ID_72720 Human_SNP_ID_590917580 m1A Human chr16 - 1367627 1367627 1367627 GCAGGTGAGTGTGTGGGGGGGCCAGACAGGTGAGGGGGAGGGAGGGCCGCAGGGGACTCAGGTGA GCAGGTGAGTGTGTGGGGGGGCCAGACAGGTGGGGGGGAGGGAGGGCCGCAGGGGACTCAGGTGA T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1367625..1367853 26863196 MeRIP-seq:(Medium) rs1466922105 Functional Loss SNV dbSNP153 33..33 33 - - - 72721 RMVar_ID_72721 Human_SNP_ID_590917644 m1A Human chr16 - 1367724 1367724 1367724 CAAGTCCAAACGGAGCTGAGCTGGCCCGGGTCAGGCGGCAGCTGGACGAGGCCAAGAGGAAGATC CAAGTCCAAACGGAGCTGAGCTGGCCCGGGTCCGGCGGCAGCTGGACGAGGCCAAGAGGAAGATC T G UNKL Ensembl:ENSG00000059145 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1367163..1367804 26863196 MeRIP-seq:(Medium) rs567668351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8427858,Human_RBP_ID_18984950,Human_RBP_ID_22944947,Human_RBP_ID_23678972 Human_Splice_Rec_1659023,Human_Splice_Rec_1659051,Human_Splice_Rec_1659061,Human_Splice_Rec_1659073,Human_Splice_Rec_1659083,Human_Splice_Rec_1659111,Human_Splice_Rec_1659115,Human_Splice_Rec_1659125 72722 RMVar_ID_72722 Human_SNP_ID_590918806 m1A Human chr16 + 1370247 1370247 1370247 TGAGGAGCCCACCGGCCCTGGGAGGGGCTGGGACAGCGAACCGAGCGGCGAGGTGGACGCAGAGG TGAGGAGCCCACCGGCCCTGGGAGGGGCTGGGGCAGCGAACCGAGCGGCGAGGTGGACGCAGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1370070..1370416 26863196 MeRIP-seq:(Medium) rs868282205 Functional Loss SNV dbSNP153 33..33 33 - - - 72723 RMVar_ID_72723 Human_SNP_ID_590918825 m1A Human chr16 + 1370275 1370275 1370275 TGGGACAGCGAACCGAGCGGCGAGGTGGACGCAGAGGATGGCGAGTGTAGCGATGGTGCTCTGGG TGGGACAGCGAACCGAGCGGCGAGGTGGACGCGGAGGATGGCGAGTGTAGCGATGGTGCTCTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1369988..1370350 26863196 MeRIP-seq:(Medium) rs1270133326 Functional Loss SNV dbSNP153 33..33 33 - - - 72724 RMVar_ID_72724 Human_SNP_ID_590920199 m1A Human chr16 + 1374206 1374206 1374206 CGCACAGAGACCTCAGCAGCGTGGGGCACACCACACAGGGACTGTTGCGCAGGCGCCCTCCCCGC CGCACAGAGACCTCAGCAGCGTGGGGCACACCGCACAGGGACTGTTGCGCAGGCGCCCTCCCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1374201..1374453 26863196 MeRIP-seq:(Medium) rs1175131567 Functional Loss SNV dbSNP153 33..33 33 - - - 72725 RMVar_ID_72725 Human_SNP_ID_590920257 m1A Human chr16 - 1374354 1374354 1374354 GTCTCAGAGCAGGCCTCAGCAGCACACTGTCCAGTACCAGGCATCAGTGAGGGTCCAAGAACTTG GTCTCAGAGCAGGCCTCAGCAGCACACTGTCCGGTACCAGGCATCAGTGAGGGTCCAAGAACTTG T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1374315..1374400 26863196 MeRIP-seq:(Medium) rs1289402919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8187611,Human_RBP_ID_8941476,Human_RBP_ID_12669404,Human_RBP_ID_18481783,Human_RBP_ID_22739180 RMVar_hsa_circ_175482,RMVar_hsa_circ_61223 72726 RMVar_ID_72726 Human_SNP_ID_590920878 m1A Human chr16 + 1375861 1375861 1375861 GCGTCCCTGAGCGGACATCCACCCTGGCCTGCAGGGTGGGCCAGCCCTCCCGGTCGCTGTCATCC GCGTCCCTGAGCGGACATCCACCCTGGCCTGCGGGGTGGGCCAGCCCTCCCGGTCGCTGTCATCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1375859..1376013 32194978 MeRIP-seq:(Medium) rs1297224355 Functional Loss SNV dbSNP153 33..33 33 - - - 72727 RMVar_ID_72727 Human_SNP_ID_590921075 m1A Human chr16 - 1376325 1376323 1376326 CCCAGCCCTAGAGTGAGGGAGGAGGGAAGAGGAGTGCCCCAGCCCTGGAGGGAGGAGGGAGAGTG CCCAGCCCTAGAGTGAGGGAGGAGGGAAGAG___TGCCCCAGCCCTGGAGGGAGGAGGGAGAGTG ACTC A UNKL Ensembl:ENSG00000059145 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1376020..1376645 26863196 MeRIP-seq:(Medium) rs892720861 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_261306,Human_RBP_ID_816564,Human_RBP_ID_3508760,Human_RBP_ID_5141771,Human_RBP_ID_5317236,Human_RBP_ID_8184118,Human_RBP_ID_8231217,Human_RBP_ID_9419576,Human_RBP_ID_21972181 RMVar_hsa_circ_61223 72728 RMVar_ID_72728 Human_SNP_ID_590921079 m1A Human chr16 - 1376328 1376328 1376328 CACCCCAGCCCTAGAGTGAGGGAGGAGGGAAGAGGAGTGCCCCAGCCCTGGAGGGAGGAGGGAGA CACCCCAGCCCTAGAGTGAGGGAGGAGGGAAGCGGAGTGCCCCAGCCCTGGAGGGAGGAGGGAGA T G UNKL Ensembl:ENSG00000059145 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:1376085..1376567;chr16:1376055..1376676 26863196 MeRIP-seq:(Medium) rs1189612408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261306,Human_RBP_ID_816564,Human_RBP_ID_3508760,Human_RBP_ID_5141771,Human_RBP_ID_8184118,Human_RBP_ID_8231217,Human_RBP_ID_9419576,Human_RBP_ID_21972181 RMVar_hsa_circ_61223 72729 RMVar_ID_72729 Human_SNP_ID_590921809 m1A Human chr16 - 1378544 1378544 1378544 CCACATGCTGCGCACTCTGCAGCTGGTGGGTGAAGCTTCTGCCGACTTAGCACGGAGCCTGGTGG CCACATGCTGCGCACTCTGCAGCTGGTGGGTGGAGCTTCTGCCGACTTAGCACGGAGCCTGGTGG T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1378497..1378716 32194978 MeRIP-seq:(Medium) rs1465071652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45989 RMVar_hsa_circ_61223 72730 RMVar_ID_72730 Human_SNP_ID_590924067 m1A Human chr16 + 1385224 1385224 1385224 ACGGTGCTGGACTTACCGAGGACGGCCTCCACAGTGCTGCTGGCGGGGCCGAGCGGGAGGGCACG ACGGTGCTGGACTTACCGAGGACGGCCTCCACGGTGCTGCTGGCGGGGCCGAGCGGGAGGGCACG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1385222..1385362 26863196 MeRIP-seq:(Medium) rs754079993 Functional Loss SNV dbSNP153 33..33 33 - - - 72731 RMVar_ID_72731 Human_SNP_ID_590934524 m1A Human chr16 + 1414020 1414019 1414021 GCCGGTGCTGCGCGCACTTGTGCTGTGAAAACAGGGGGCACTGCTCCGTCCTGAACTCCTTCAGG GCCGGTGCTGCGCGCACTTGTGCTGTGAAAAC__GGGGCACTGCTCCGTCCTGAACTCCTTCAGG CAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:1413919..1414047 26863196 MeRIP-seq:(Medium) rs1219580427 Functional Loss DEL dbSNP153 33..34 33 - - - 72732 RMVar_ID_72732 Human_SNP_ID_590936685 m1A Human chr16 - 1420262 1420262 1420262 TCGTTCTGAGGAGCCTGAGACTCCAGCTGCCTACAGAGCGAGAACTTGACGGGGTGCCCGCTGGG TCGTTCTGAGGAGCCTGAGACTCCAGCTGCCTGCAGAGCGAGAACTTGACGGGGTGCCCGCTGGG T C C16orf91 Ensembl:ENSG00000174109 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1420213..1420320 26863196 MeRIP-seq:(Medium) rs1212783880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4351117 RMVar_hsa_circ_99247,RMVar_hsa_circ_175487 72733 RMVar_ID_72733 Human_SNP_ID_590936699 m1A Human chr16 + 1420288 1420288 1420288 GCTCTGTAGGCAGCTGGAGTCTCAGGCTCCTCAGAACGATCACTGGGCTCTGGCACCTCTCCCCA GCTCTGTAGGCAGCTGGAGTCTCAGGCTCCTCCGAACGATCACTGGGCTCTGGCACCTCTCCCCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:1420167..1420360 26863196 MeRIP-seq:(Medium) rs770819946 Functional Loss SNV dbSNP153 33..33 33 - - - 72734 RMVar_ID_72734 Human_SNP_ID_590936705 m1A Human chr16 + 1420310 1420310 1420310 CAGGCTCCTCAGAACGATCACTGGGCTCTGGCACCTCTCCCCACACCTGTCTCAACCACTGGTCC CAGGCTCCTCAGAACGATCACTGGGCTCTGGCGCCTCTCCCCACACCTGTCTCAACCACTGGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:1420153..1420393;chr16:1420156..1420387 26863196 MeRIP-seq:(Medium) rs1281963199 Functional Loss SNV dbSNP153 33..33 33 - - - 72735 RMVar_ID_72735 Human_SNP_ID_590936707 m1A Human chr16 - 1420313 1420313 1420313 GGCGGACCAGTGGTTGAGACAGGTGTGGGGAGAGGTGCCAGAGCCCAGTGATCGTTCTGAGGAGC GGCGGACCAGTGGTTGAGACAGGTGTGGGGAGGGGTGCCAGAGCCCAGTGATCGTTCTGAGGAGC T C C16orf91 Ensembl:ENSG00000174109 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1420213..1420329 26863196 MeRIP-seq:(Medium) rs764773204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234147,Human_RBP_ID_4392739,Human_RBP_ID_22054808,Human_RBP_ID_22442325 RMVar_hsa_circ_99247,RMVar_hsa_circ_175488,RMVar_hsa_circ_175487 72736 RMVar_ID_72736 Human_SNP_ID_590936831 m1A Human chr16 + 1420531 1420531 1420531 GGGCGGTCAGGGTCGTCCTCTTCCTCGGCGGCAGGGTGGGCCCGATCCCGGGAACCGGGCAACGG GGGCGGTCAGGGTCGTCCTCTTCCTCGGCGGCGGGGTGGGCCCGATCCCGGGAACCGGGCAACGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1420483..1420727 26863196 MeRIP-seq:(Medium) rs1567251615 Functional Loss SNV dbSNP153 33..33 33 - - - 72737 RMVar_ID_72737 Human_SNP_ID_590936883 m1A Human chr16 - 1420614 1420614 1420614 GCGGGCGGAGCGCTTACTGCTCTCTCTCTTCCAGGGCCGTCCGGGCGCTGAGGCTCATAGGCTGG GCGGGCGGAGCGCTTACTGCTCTCTCTCTTCCGGGGCCGTCCGGGCGCTGAGGCTCATAGGCTGG T C C16orf91 Ensembl:ENSG00000174109 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1420517..1420654 26863410 MeRIP-seq:(Medium) rs1567251675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277231,Human_RBP_ID_891099,Human_RBP_ID_4392741,Human_RBP_ID_5180962,Human_RBP_ID_5440158,Human_RBP_ID_5495125,Human_RBP_ID_17871972 RMVar_hsa_circ_99247,RMVar_hsa_circ_175487 72738 RMVar_ID_72738 Human_SNP_ID_590943439 m1A Human chr16 + 1438813 1438813 1438813 CGGCCCCACCTGCCCGCCGCCCGCCCGGCCCCACCTCATGCTGCCCCTGCAGGGCCCGCAGGCGC CGGCCCCACCTGCCCGCCGCCCGCCCGGCCCCCCCTCATGCTGCCCCTGCAGGGCCCGCAGGCGC A C AL032819.2 Ensembl:ENSG00000279930 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1438807..1439125 26863196 MeRIP-seq:(Medium) rs1469937315 Functional Loss SNV dbSNP153 33..33 33 - - - 72739 RMVar_ID_72739 Human_SNP_ID_590946312 m1A Human chr16 - 1445923 1445923 1445923 AGCTGAGAAAAACCTCCAAGGCCCTGAGCCCCATGCCCAGCCCTGCCTTGGTCCCCCAACCCCCA AGCTGAGAAAAACCTCCAAGGCCCTGAGCCCCGTGCCCAGCCCTGCCTTGGTCCCCCAACCCCCA T C CLCN7 Ensembl:ENSG00000103249 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1445874..1445974 26863196 MeRIP-seq:(Medium) rs916047304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763176,Human_RBP_ID_5113791,Human_RBP_ID_5316462,Human_RBP_ID_17078472,Human_RBP_ID_18161967,Human_RBP_ID_26445598,Human_RBP_ID_27439207 72740 RMVar_ID_72740 Human_SNP_ID_590946471 m1A Human chr16 + 1446350 1446348 1446350 TCCCAAGAGGCCGATAGCCCGGTAGGGAGGTCACACACACACAGCTGATCCCTGGAGGTAAAGAA TCCCAAGAGGCCGATAGCCCGGTAGGGAGGT__CACACACACAGCTGATCCCTGGAGGTAAAGAA TCA T AL031600.3 Ensembl:ENSG00000261641 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1446300..1446435 26863196 MeRIP-seq:(Medium) rs367705655 Functional Loss DEL dbSNP153 32..33 33 - - - 72741 RMVar_ID_72741 Human_SNP_ID_590946561 m1A Human chr16 - 1446479 1446479 1446479 CCTGCAGCTGGGCGGGCAGGCGGCAGGCGCGGAACTGACCCTCTCGCGGGACTGACCCTGTTGTG CCTGCAGCTGGGCGGGCAGGCGGCAGGCGCGGGACTGACCCTCTCGCGGGACTGACCCTGTTGTG T C CLCN7 Ensembl:ENSG00000103249 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1446428..1446541 26863196 MeRIP-seq:(Medium) rs1350371020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_641991 72742 RMVar_ID_72742 Human_SNP_ID_590947488 m1A Human chr16 - 1448477 1448477 1448477 ATGTGTGGCCGGGCTCCTCCGGCAGGGAGGTGATGAGCACACCAGTGACCTGCCTGAGGCGGCGT ATGTGTGGCCGGGCTCCTCCGGCAGGGAGGTGTTGAGCACACCAGTGACCTGCCTGAGGCGGCGT T A CLCN7 Ensembl:ENSG00000103249 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1448426..1448527 32194978 MeRIP-seq:(Medium) rs1274966207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1659262,Human_Splice_Rec_1659308,Human_Splice_Rec_1659352,Human_Splice_Rec_1659362,Human_Splice_Rec_1659406,Human_Splice_Rec_1659424 RMVar_hsa_circ_8614,RMVar_hsa_circ_82222,RMVar_hsa_circ_106712,RMVar_hsa_circ_175489,RMVar_hsa_circ_175490 72743 RMVar_ID_72743 Human_SNP_ID_590949066 m1A Human chr16 - 1452256 1452256 1452256 AAACATCCAGAACAGGGAGAGCCTAGAGGCCCAGCAGACCAGTGGGTGCCACGGCGGGAGTGGGC AAACATCCAGAACAGGGAGAGCCTAGAGGCCCGGCAGACCAGTGGGTGCCACGGCGGGAGTGGGC T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1452210..1452311 26863196 MeRIP-seq:(Medium) rs890118294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8231771,Human_RBP_ID_22651364,Human_RBP_ID_27837704 RMVar_hsa_circ_8614,RMVar_hsa_circ_82222,RMVar_hsa_circ_175489,RMVar_hsa_circ_116060,RMVar_hsa_circ_175491 72744 RMVar_ID_72744 Human_SNP_ID_590951823 m1A Human chr16 + 1459346 1459309 1459346 CAGCACACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCAGCACACACGTCAGGGCCCCAGGGAAG _________________________________AGAGCAGCACACACGTCAGGGCCCCAGGGAAG GAGCTCAGCACACAAACGTCGGGGCCCCAGGGAAGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1459327..1459503 26863196 MeRIP-seq:(Medium) rs1567271308 Functional Loss DEL dbSNP153 1..33 33 - - - 72745 RMVar_ID_72745 Human_SNP_ID_590951851 m1A Human chr16 + 1459346 1459344 1459347 CAGCACACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCAGCACACACGTCAGGGCCCCAGGGAAG CAGCACACAAACGTCGGGGCCCCAGGGAAGG___GAGCAGCACACACGTCAGGGCCCCAGGGAAG GGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1459327..1459503 26863196 MeRIP-seq:(Medium) rs1218651508 Functional Loss DEL dbSNP153 32..34 33 - - - 72746 RMVar_ID_72746 Human_SNP_ID_590951852 m1A Human chr16 + 1459346 1459345 1459347 CAGCACACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCAGCACACACGTCAGGGCCCCAGGGAAG CAGCACACAAACGTCGGGGCCCCAGGGAAGGG__GAGCAGCACACACGTCAGGGCCCCAGGGAAG GAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1459327..1459503 26863196 MeRIP-seq:(Medium) rs1299301156 Functional Loss DEL dbSNP153 33..34 33 - - - 72747 RMVar_ID_72747 Human_SNP_ID_590951853 m1A Human chr16 + 1459346 1459346 1459346 CAGCACACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCAGCACACACGTCAGGGCCCCAGGGAAG CAGCACACAAACGTCGGGGCCCCAGGGAAGGGGAGAGCAGCACACACGTCAGGGCCCCAGGGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1459327..1459503 26863196 MeRIP-seq:(Medium) rs1301482751 Functional Loss SNV dbSNP153 33..33 33 - - - 72748 RMVar_ID_72748 Human_SNP_ID_590951860 m1A Human chr16 + 1459352 1459352 1459352 ACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCAGCACACACGTCAGGGCCCCAGGGAAGGGGAGA ACAAACGTCGGGGCCCCAGGGAAGGGAAGAGCGGCACACACGTCAGGGCCCCAGGGAAGGGGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1459342..1459491 26863196 MeRIP-seq:(Medium) rs1487869956 Functional Loss SNV dbSNP153 33..33 33 - - - 72749 RMVar_ID_72749 Human_SNP_ID_590951922 m1A Human chr16 + 1459429 1459429 1459429 TCGGGGCCCCAGGGAAGGGGAGCTCAGCACACACGTCGGGGCATCAGGGAAGGGGAGAGCAGCAC TCGGGGCCCCAGGGAAGGGGAGCTCAGCACACGCGTCGGGGCATCAGGGAAGGGGAGAGCAGCAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1459278..1459490 26863196 MeRIP-seq:(Medium) rs1335640040 Functional Loss SNV dbSNP153 33..33 33 - - - 72750 RMVar_ID_72750 Human_SNP_ID_590952073 m1A Human chr16 - 1459895 1459790 1459895 CCCCGACGTGTGTGCTGCTCTCCCCTTCCCTGAGGCCCCGACATGTGTGCTGAGCTCCCCTTCCC CCCCGACGTGTGTGCTGCTCTCCCCTTCCCTG_________________________________ CCAGGGAAGGGGAGAGCGGCACACACGTCGGGGCCTCAGGGAAGGGGAGCTCAGCACACACGTCGGGGCCCCAGGGAAGGGGAGCTCAGCACACATGTCGGGGCCT C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1459851..1460005 26863196 MeRIP-seq:(Medium) rs71376595 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_1089420,Human_RBP_ID_8086692,Human_RBP_ID_17563677,Human_RBP_ID_23679435 RMVar_hsa_circ_8614,RMVar_hsa_circ_82222,RMVar_hsa_circ_175489,RMVar_hsa_circ_116060,RMVar_hsa_circ_175491,RMVar_hsa_circ_79811,RMVar_hsa_circ_175494,RMVar_hsa_circ_20074,RMVar_hsa_circ_34264,RMVar_hsa_circ_44657,RMVar_hsa_circ_278086,RMVar_hsa_circ_338075 72751 RMVar_ID_72751 Human_SNP_ID_590952118 m1A Human chr16 - 1459895 1459895 1459895 CCCCGACGTGTGTGCTGCTCTCCCCTTCCCTGAGGCCCCGACATGTGTGCTGAGCTCCCCTTCCC CCCCGACGTGTGTGCTGCTCTCCCCTTCCCTGGGGCCCCGACATGTGTGCTGAGCTCCCCTTCCC T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1459851..1460005 26863196 MeRIP-seq:(Medium) rs1330048998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089420,Human_RBP_ID_8086692,Human_RBP_ID_17563677,Human_RBP_ID_23679435 RMVar_hsa_circ_8614,RMVar_hsa_circ_82222,RMVar_hsa_circ_175489,RMVar_hsa_circ_116060,RMVar_hsa_circ_175491,RMVar_hsa_circ_79811,RMVar_hsa_circ_175494,RMVar_hsa_circ_20074,RMVar_hsa_circ_34264,RMVar_hsa_circ_44657,RMVar_hsa_circ_278086,RMVar_hsa_circ_338075 72752 RMVar_ID_72752 Human_SNP_ID_590954041 m1A Human chr16 - 1464987 1464987 1464987 GAGGGGGCTGGACCTGGCTTTGGGACAGGGCAAGGACAGGGATCTTGGGGGGGCAGTGAGGAGCC GAGGGGGCTGGACCTGGCTTTGGGACAGGGCAGGGACAGGGATCTTGGGGGGGCAGTGAGGAGCC T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1464985..1465147 26863196 MeRIP-seq:(Medium) rs889969877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8614,RMVar_hsa_circ_82222,RMVar_hsa_circ_175489,RMVar_hsa_circ_116060,RMVar_hsa_circ_175491,RMVar_hsa_circ_20074,RMVar_hsa_circ_278086,RMVar_hsa_circ_284779,RMVar_hsa_circ_311691 72753 RMVar_ID_72753 Human_SNP_ID_590957225 m1A Human chr16 - 1474560 1474560 1474560 GCTCGCCAGACCCCGCGGAATGTGGGGCGCTGAGGGGCGCCGGGGCAGCCGTGGCGCACGTTCAT GCTCGCCAGACCCCGCGGAATGTGGGGCGCTGGGGGGCGCCGGGGCAGCCGTGGCGCACGTTCAT T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1474558..1474722 26863196 MeRIP-seq:(Medium) rs879502417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17123697 72754 RMVar_ID_72754 Human_SNP_ID_590957377 m1A Human chr16 + 1474868 1474868 1474868 GGCGCGCAGCCCCAGGCCCAGCCCCGTTCAGCAGCGGCGTCCCCCCGCCGGGCCGCGCCGTCCTC GGCGCGCAGCCCCAGGCCCAGCCCCGTTCAGCCGCGGCGTCCCCCCGCCGGGCCGCGCCGTCCTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:1474826..1475025 26863196 MeRIP-seq:(Medium) rs1228740943 Functional Loss SNV dbSNP153 33..33 33 - - - 72755 RMVar_ID_72755 Human_SNP_ID_590957398 m1A Human chr16 - 1474896 1474896 1474896 ACGACGAGGAGGCGGCGCCGCTGCTGCGGAGGACGGCGCGGCCCGGCGGGGGGACGCCGCTGCTG ACGACGAGGAGGCGGCGCCGCTGCTGCGGAGGGCGGCGCGGCCCGGCGGGGGGACGCCGCTGCTG T C CLCN7 Ensembl:ENSG00000103249 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr16:1474364..1475025;chr16:1474773..1475050;chr16:1474364..1475050;chr16:1474364..1474982 26863196,32194978 MeRIP-seq:(Medium) rs1158311054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4351611,Human_RBP_ID_22944792 Human_Splice_Rec_1659269,Human_Splice_Rec_1659315,Human_Splice_Rec_1659369,Human_Splice_Rec_1659451,Human_Splice_Rec_1659457,Human_Splice_Rec_1659473 72756 RMVar_ID_72756 Human_SNP_ID_590957633 m1A Human chr16 + 1475387 1475387 1475387 TCCCCCAGGCCCGGTCGCCCGCGCCGATCGTGACGGAGCCGCGGTGGGGAAGGGAGGAGGGAGGC TCCCCCAGGCCCGGTCGCCCGCGCCGATCGTGGCGGAGCCGCGGTGGGGAAGGGAGGAGGGAGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1475204..1475463 26863196 MeRIP-seq:(Medium) rs1349241900 Functional Loss SNV dbSNP153 33..33 33 - - - 72757 RMVar_ID_72757 Human_SNP_ID_590963761 m1A Human chr16 + 1494301 1494300 1494301 TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGAGGTTCGACTCGCCGTCCGGGAAGCCATTCATG TCTGTCCTGCAGGATGGAGCCAGCACCCTCACGGGTTCGACTCGCCGTCCGGGAAGCCATTCATG GA CG TELO2 Ensembl:ENSG00000100726 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35400877 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_4393452 Human_Splice_Rec_1659484,Human_Splice_Rec_1659504 RMVar_hsa_circ_335860 72758 RMVar_ID_72758 Human_SNP_ID_590963762 m1A Human chr16 + 1494301 1494300 1494301 TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGAGGTTCGACTCGCCGTCCGGGAAGCCATTCATG TCTGTCCTGCAGGATGGAGCCAGCACCCTCAG_GGTTCGACTCGCCGTCCGGGAAGCCATTCATG GA G TELO2 Ensembl:ENSG00000100726 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879420987 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4393452 Human_Splice_Rec_1659484,Human_Splice_Rec_1659504 RMVar_hsa_circ_335860 72759 RMVar_ID_72759 Human_SNP_ID_590963763 m1A Human chr16 + 1494301 1494301 1494301 TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGAGGTTCGACTCGCCGTCCGGGAAGCCATTCATG TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGGGGTTCGACTCGCCGTCCGGGAAGCCATTCATG A G TELO2 Ensembl:ENSG00000100726 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2667661 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4393452 Human_Splice_Rec_1659484,Human_Splice_Rec_1659504 GWAS_ID_8862,GWAS_ID_8863 RMVar_hsa_circ_335860 72760 RMVar_ID_72760 Human_SNP_ID_590966270 m1A Human chr16 - 1500595 1500595 1500595 TCGCACGGGGGGCAGGCTACTGTCCAGGCGGCACTTCACGCCCGCCATCATGCTGGCCAGCAGTT TCGCACGGGGGGCAGGCTACTGTCCAGGCGGCGCTTCACGCCCGCCATCATGCTGGCCAGCAGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1500473..1500740 26863196 MeRIP-seq:(Medium) rs1056022419 Functional Loss SNV dbSNP153 33..33 33 - - - 72761 RMVar_ID_72761 Human_SNP_ID_590966320 m1A Human chr16 + 1500698 1500698 1500698 GATCCACCCCGAGGGGCCTCCCCTGAAATTCCAGGTGAGCGGGCCGTCCCCTCCGCGTCCCCGTG GATCCACCCCGAGGGGCCTCCCCTGAAATTCCGGGTGAGCGGGCCGTCCCCTCCGCGTCCCCGTG A G TELO2 Ensembl:ENSG00000100726 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1500598..1500758 26863410 MeRIP-seq:(Medium) rs769020185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070426 Human_Splice_Rec_1659519 RMVar_hsa_circ_11811,RMVar_hsa_circ_116150,RMVar_hsa_circ_335860,RMVar_hsa_circ_269165,RMVar_hsa_circ_51722,RMVar_hsa_circ_175498,RMVar_hsa_circ_118219,RMVar_hsa_circ_175499 72762 RMVar_ID_72762 Human_SNP_ID_590968542 m1A Human chr16 - 1506193 1506193 1506193 ACTACAGCGATCACGGAGGTGCAGGCTTGGGCAGCGGGCACGGCACCCCTAGCCCGAGAGGATCC ACTACAGCGATCACGGAGGTGCAGGCTTGGGCTGCGGGCACGGCACCCCTAGCCCGAGAGGATCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1506189..1506254 26863196 MeRIP-seq:(Medium) rs1293286101 Functional Loss SNV dbSNP153 33..33 33 - - - 72763 RMVar_ID_72763 Human_SNP_ID_590968579 m1A Human chr16 + 1506265 1506265 1506265 GGCAGGGTGGCCCGAGGCAGGGCCCGGCAGGCAGCCCCAGCAGATTCAACTCCGTGGCCGGCCAC GGCAGGGTGGCCCGAGGCAGGGCCCGGCAGGCGGCCCCAGCAGATTCAACTCCGTGGCCGGCCAC A G TELO2 Ensembl:ENSG00000100726 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1506167..1506265 26863196 MeRIP-seq:(Medium) rs1383139767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818568 Human_Splice_Rec_1659499,Human_Splice_Rec_1659534,Human_Splice_Rec_1659535,Human_Splice_Rec_1659554,Human_Splice_Rec_1659555,Human_Splice_Rec_1659566,Human_Splice_Rec_1659570,Human_Splice_Rec_1659571,Human_Splice_Rec_1659574,Human_Splice_Rec_1659575,Human_Splice_Rec_1659578 RMVar_hsa_circ_116150,RMVar_hsa_circ_335860,RMVar_hsa_circ_25500,RMVar_hsa_circ_94017,RMVar_hsa_circ_175498,RMVar_hsa_circ_118219,RMVar_hsa_circ_175499,RMVar_hsa_circ_111412,RMVar_hsa_circ_175500,RMVar_hsa_circ_88212,RMVar_hsa_circ_175501,RMVar_hsa_circ_175502,RMVar_hsa_circ_30704,RMVar_hsa_circ_118482,RMVar_hsa_circ_175504,RMVar_hsa_circ_106055,RMVar_hsa_circ_175505,RMVar_hsa_circ_325091 72764 RMVar_ID_72764 Human_SNP_ID_590969030 m1A Human chr16 - 1507368 1507368 1507368 TGGCCTGGCCCAGCCCCACAGGCCACTCACGCATCGATGTGGAAGCGAAGGGCCCACACGAATTC TGGCCTGGCCCAGCCCCACAGGCCACTCACGCGTCGATGTGGAAGCGAAGGGCCCACACGAATTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1506762..1510008 32194978 MeRIP-seq:(Medium) rs1471917352 Functional Loss SNV dbSNP153 33..33 33 - - - 72765 RMVar_ID_72765 Human_SNP_ID_590969171 m1A Human chr16 - 1507655 1507655 1507655 TCGTCCATCAGGTCCTCCAGCAGGCGCGCAGCAGGCAGGCTGAGCAGGACGGAGGAGACGGCCGA TCGTCCATCAGGTCCTCCAGCAGGCGCGCAGCGGGCAGGCTGAGCAGGACGGAGGAGACGGCCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1507564..1507658 26863196 MeRIP-seq:(Medium) rs1288772159 Functional Loss SNV dbSNP153 33..33 33 - - - 72766 RMVar_ID_72766 Human_SNP_ID_590969229 m1A Human chr16 - 1507748 1507746 1507748 CACACATACACACACACCCCGGGCCGACACACATCTCACACACACACCGCAGGCCGACACTCACC CACACATACACACACACCCCGGGCCGACACAC__CTCACACACACACCGCAGGCCGACACTCACC GAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1507723..1507963 26863196 MeRIP-seq:(Medium) rs1296928106 Functional Loss DEL dbSNP153 33..34 33 - - - 72767 RMVar_ID_72767 Human_SNP_ID_590970278 m1A Human chr16 + 1510220 1510220 1510220 CTGGCGGGGTTGACTCTTCCAGTGAGGGCAGAACCAGGCTGGCAGGAGGGGAGGACGGTGTACCT CTGGCGGGGTTGACTCTTCCAGTGAGGGCAGACCCAGGCTGGCAGGAGGGGAGGACGGTGTACCT A C TELO2 Ensembl:ENSG00000100726 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1510170..1510408 26863196 MeRIP-seq:(Medium) rs1001533259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17653206,Human_RBP_ID_18161977,Human_RBP_ID_20098455,Human_RBP_ID_21971826 Human_miRNA_ID_2398088 RMVar_hsa_circ_116150,RMVar_hsa_circ_94017,RMVar_hsa_circ_175498,RMVar_hsa_circ_118219,RMVar_hsa_circ_175499,RMVar_hsa_circ_111412,RMVar_hsa_circ_175500,RMVar_hsa_circ_88212,RMVar_hsa_circ_175501,RMVar_hsa_circ_175502,RMVar_hsa_circ_118482,RMVar_hsa_circ_175504,RMVar_hsa_circ_106055,RMVar_hsa_circ_175505,RMVar_hsa_circ_101636,RMVar_hsa_circ_109024,RMVar_hsa_circ_175507,RMVar_hsa_circ_175508 72768 RMVar_ID_72768 Human_SNP_ID_590975332 m1A Human chr16 - 1524800 1524800 1524800 CCACTTCTCCCTGGTCCGCATCCACTGCTTCCAGGGCAATGTCCAGAAGGTAAGGTCCCCGCAGG CCACTTCTCCCTGGTCCGCATCCACTGCTTCCGGGGCAATGTCCAGAAGGTAAGGTCCCCGCAGG T C IFT140 Ensembl:ENSG00000187535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1524318..1525918 32194978 MeRIP-seq:(Medium) rs746546785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1659593,Human_Splice_Rec_1659653,Human_Splice_Rec_1659691,Human_Splice_Rec_1659735 RMVar_hsa_circ_18196,RMVar_hsa_circ_175511,RMVar_hsa_circ_84860 72769 RMVar_ID_72769 Human_SNP_ID_590976162 m1A Human chr16 - 1526710 1526710 1526710 CGTGGCCAAGGTGTGCCTGGGGAACATGGGCCATGCCCGCGGGGCCCGAGCGCTGCGTGAGGCGG CGTGGCCAAGGTGTGCCTGGGGAACATGGGCCGTGCCCGCGGGGCCCGAGCGCTGCGTGAGGCGG T C IFT140 Ensembl:ENSG00000187535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1526664..1526765 32194978 MeRIP-seq:(Medium) rs1275107709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18982921 Human_Splice_Rec_1659586,Human_Splice_Rec_1659587,Human_Splice_Rec_1659646,Human_Splice_Rec_1659647,Human_Splice_Rec_1659686,Human_Splice_Rec_1659728 RMVar_hsa_circ_18196,RMVar_hsa_circ_175511,RMVar_hsa_circ_84860 72770 RMVar_ID_72770 Human_SNP_ID_590980260 m1A Human chr16 - 1539160 1539160 1539160 GGCCCAAGGCGTGGGGCGGCGTGGCACTGTGCAGCTTGGTGAGGCCTGAGGCGTGGGGCCGTCTG GGCCCAAGGCGTGGGGCGGCGTGGCACTGTGCGGCTTGGTGAGGCCTGAGGCGTGGGGCCGTCTG T C IFT140 Ensembl:ENSG00000187535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1539148..1539230 26863196 MeRIP-seq:(Medium) rs906963277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22712147 RMVar_hsa_circ_175511,RMVar_hsa_circ_84860 72771 RMVar_ID_72771 Human_SNP_ID_590995848 m1A Human chr16 - 1592307 1592307 1592307 TCGTGTCGTGTTTGCTTTCAGGGACCTGGTTCAGTTGGCAAAGGCAGCTGTGAGCGGTGATGAGA TCGTGTCGTGTTTGCTTTCAGGGACCTGGTTCGGTTGGCAAAGGCAGCTGTGAGCGGTGATGAGA T C IFT140 Ensembl:ENSG00000187535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1592257..1602533 32194978 MeRIP-seq:(Medium) rs1178715117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4352253,Human_RBP_ID_5523864,Human_RBP_ID_18985010,Human_RBP_ID_19070443 Human_Splice_Rec_1659618,Human_Splice_Rec_1659766 RMVar_hsa_circ_175511,RMVar_hsa_circ_84860,RMVar_hsa_circ_350366,RMVar_hsa_circ_175513,RMVar_hsa_circ_62596,RMVar_hsa_circ_48449,RMVar_hsa_circ_265998,RMVar_hsa_circ_332077,RMVar_hsa_circ_175517,RMVar_hsa_circ_175516,RMVar_hsa_circ_303767 72772 RMVar_ID_72772 Human_SNP_ID_591002523 m1A Human chr16 - 1612415 1612415 1612415 GGACGCAGATACTGCCGCCACTCACCCTAGCGAAGCCGGCCCGCCGCCCTCAGCAGCAGTTCCGG GGACGCAGATACTGCCGCCACTCACCCTAGCGGAGCCGGCCCGCCGCCCTCAGCAGCAGTTCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1612403..1612686 26863196 MeRIP-seq:(Medium) rs538504578 Functional Loss SNV dbSNP153 33..33 33 - - - 72773 RMVar_ID_72773 Human_SNP_ID_591003466 m1A Human chr16 + 1614761 1614761 1614761 AGAAGGGGCCGGCGGCGCAGACGCGGCCGAGGAGAGCAGCGGCACAAAGAGGGACGAGAAGACCC AGAAGGGGCCGGCGGCGCAGACGCGGCCGAGGCGAGCAGCGGCACAAAGAGGGACGAGAAGACCC A C CRAMP1 Ensembl:ENSG00000007545 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1614588..1632221 26863196 MeRIP-seq:(Medium) rs1349986954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26684,RMVar_hsa_circ_333886,RMVar_hsa_circ_360965,RMVar_hsa_circ_175520,RMVar_hsa_circ_75552,RMVar_hsa_circ_376424,RMVar_hsa_circ_175519 72774 RMVar_ID_72774 Human_SNP_ID_591003517 m1A Human chr16 - 1614847 1614847 1614847 GTGCTGGTCCTGGGGGCTGCCCTGCGGCGGGGACGGCGCCTGCGGCGCGCCGGGGGGCGCGGGGG GTGCTGGTCCTGGGGGCTGCCCTGCGGCGGGGGCGGCGCCTGCGGCGCGCCGGGGGGCGCGGGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1614668..1614852 26863410 MeRIP-seq:(Medium) rs1396748134 Functional Loss SNV dbSNP153 33..33 33 - - - 72775 RMVar_ID_72775 Human_SNP_ID_591003555 m1A Human chr16 + 1614937 1614934 1614937 CGCAGAGCAAGAGGCCCAGGAAGGATCCTCCGAGCGCTGTGGGGAGCGGCAACGCCGGTGGCTCG CGCAGAGCAAGAGGCCCAGGAAGGATCCTC___GCGCTGTGGGGAGCGGCAACGCCGGTGGCTCG CCGA C CRAMP1 Ensembl:ENSG00000007545 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1614890..1615076 32194978 MeRIP-seq:(Medium) rs1322802784 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_18985015 Human_Splice_Rec_1659829,Human_Splice_Rec_1659867 RMVar_hsa_circ_26684,RMVar_hsa_circ_333886,RMVar_hsa_circ_360965,RMVar_hsa_circ_175520,RMVar_hsa_circ_75552,RMVar_hsa_circ_376424,RMVar_hsa_circ_175519 72776 RMVar_ID_72776 Human_SNP_ID_591011371 m1A Human chr16 + 1641387 1641387 1641387 GACTGCGCCCAGAGCCTGTGCCTGCCCCGGGGAGGGAAGGAAGTGCCGTCTTTGGCCTCCTCCTT GACTGCGCCCAGAGCCTGTGCCTGCCCCGGGGGGGGAAGGAAGTGCCGTCTTTGGCCTCCTCCTT A G AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1641378..1641479 32194978 MeRIP-seq:(Medium) rs1335635103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175524,RMVar_hsa_circ_374387,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_42849,RMVar_hsa_circ_112301,RMVar_hsa_circ_175526,RMVar_hsa_circ_175529,RMVar_hsa_circ_115251 72777 RMVar_ID_72777 Human_SNP_ID_591014579 m1A Human chr16 + 1651933 1651930 1651934 GGAGGTCACGGGGAGGTGAACTGAGGTCACAGAGAGGTCACGTAGAAGTGGATTGAGGTCACACA GGAGGTCACGGGGAGGTGAACTGAGGTCAC____AGGTCACGTAGAAGTGGATTGAGGTCACACA CAGAG C AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:1651000..1652156;chr16:1651016..1652168 26863196 MeRIP-seq:(Medium) rs368741931 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_12676510,Human_RBP_ID_22583543 RMVar_hsa_circ_175524,RMVar_hsa_circ_374387,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_42849,RMVar_hsa_circ_112301,RMVar_hsa_circ_175526,RMVar_hsa_circ_175529,RMVar_hsa_circ_115251 72778 RMVar_ID_72778 Human_SNP_ID_591014580 m1A Human chr16 + 1651933 1651930 1651934 GGAGGTCACGGGGAGGTGAACTGAGGTCACAGAGAGGTCACGTAGAAGTGGATTGAGGTCACACA GGAGGTCACGGGGAGGTGAACTGAGGTCACAG__AGGTCACGTAGAAGTGGATTGAGGTCACACA CAGAG CAG AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:1651000..1652156;chr16:1651016..1652168 26863196 MeRIP-seq:(Medium) rs368741931 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12676510,Human_RBP_ID_22583543 RMVar_hsa_circ_175524,RMVar_hsa_circ_374387,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_42849,RMVar_hsa_circ_112301,RMVar_hsa_circ_175526,RMVar_hsa_circ_175529,RMVar_hsa_circ_115251 72779 RMVar_ID_72779 Human_SNP_ID_591016570 m1A Human chr16 + 1656988 1656988 1656988 CCTGAAGCTCATTTCCACCGAGGTCAACCCCAAGCTGGTGAGTGGGTTGGAGCCCAGCCCCTCTG CCTGAAGCTCATTTCCACCGAGGTCAACCCCACGCTGGTGAGTGGGTTGGAGCCCAGCCCCTCTG A C AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1656950..1659994 26863196 MeRIP-seq:(Medium) rs753035998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22053774 Human_Splice_Rec_1659845,Human_Splice_Rec_1659883,Human_Splice_Rec_1659961 RMVar_hsa_circ_23574,RMVar_hsa_circ_175524,RMVar_hsa_circ_374387,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_32654,RMVar_hsa_circ_175530,RMVar_hsa_circ_93092 72780 RMVar_ID_72780 Human_SNP_ID_591023163 m1A Human chr16 + 1678335 1678335 1678335 GGCGGTCGACATGTTCCAGGTCCCGGATAGCGAGGGCGGCCGCGCCGGCTCCAGGTGCGGCGCGG GGCGGTCGACATGTTCCAGGTCCCGGATAGCGGGGGCGGCCGCGCCGGCTCCAGGTGCGGCGCGG A G AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:1678271..1678397;chr16:1678276..1678415;chr16:1678276..1678630;chr16:1678276..1678421 26863196 MeRIP-seq:(Medium) rs1398183493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763054,Human_RBP_ID_4352479,Human_RBP_ID_5316472,Human_RBP_ID_9285529,Human_RBP_ID_18418632,Human_RBP_ID_19070457,Human_RBP_ID_22441685 Human_Splice_Rec_1659985,Human_Splice_Rec_1659991,Human_Splice_Rec_1659995,Human_Splice_Rec_1660005,Human_Splice_Rec_1660011,Human_Splice_Rec_1660029,Human_Splice_Rec_1660039,Human_Splice_Rec_1660049 72781 RMVar_ID_72781 Human_SNP_ID_591023175 m1A Human chr16 - 1678352 1678350 1678353 CCCGCCTCCCGTGTGCCCCGCGCCGCACCTGGAGCCGGCGCGGCCGCCCTCGCTATCCGGGACCT CCCGCCTCCCGTGTGCCCCGCGCCGCACCTG___CCGGCGCGGCCGCCCTCGCTATCCGGGACCT GCTC G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1678301..1678375 32194978 MeRIP-seq:(Medium) rs1047391783 Functional Loss DEL dbSNP153 32..34 33 - - - 72782 RMVar_ID_72782 Human_SNP_ID_591023181 m1A Human chr16 + 1678355 1678355 1678355 TCCCGGATAGCGAGGGCGGCCGCGCCGGCTCCAGGTGCGGCGCGGGGCACACGGGAGGCGGGCGG TCCCGGATAGCGAGGGCGGCCGCGCCGGCTCCTGGTGCGGCGCGGGGCACACGGGAGGCGGGCGG A T AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding intron,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1678276..1678375 26863410 MeRIP-seq:(Medium) rs955001118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235248,Human_RBP_ID_4393453,Human_RBP_ID_5316472,Human_RBP_ID_9285529,Human_RBP_ID_18418632,Human_RBP_ID_19070457,Human_RBP_ID_22441685 Human_Splice_Rec_1659985,Human_Splice_Rec_1659991,Human_Splice_Rec_1659995,Human_Splice_Rec_1660005,Human_Splice_Rec_1660011,Human_Splice_Rec_1660029,Human_Splice_Rec_1660039,Human_Splice_Rec_1660049 72783 RMVar_ID_72783 Human_SNP_ID_591023245 m1A Human chr16 + 1678534 1678534 1678534 GCCTTTCTGCGCCGCCGCCAGACCGAGGCCCGAAGCCCGAGGGGCCGCTCGCTGAGGCCCGGGCT GCCTTTCTGCGCCGCCGCCAGACCGAGGCCCGGAGCCCGAGGGGCCGCTCGCTGAGGCCCGGGCT A G AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1678524..1678644 26863196 MeRIP-seq:(Medium) rs1263355845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763055,Human_RBP_ID_1066194,Human_RBP_ID_3502378,Human_RBP_ID_5236501,Human_RBP_ID_5357288,Human_RBP_ID_5465791,Human_RBP_ID_8086700,Human_RBP_ID_8231772,Human_RBP_ID_9324807,Human_RBP_ID_9419062,Human_RBP_ID_18481854,Human_RBP_ID_19076517,Human_RBP_ID_22714154,Human_RBP_ID_24413632 72784 RMVar_ID_72784 Human_SNP_ID_591025362 m1A Human chr16 - 1685514 1685513 1685514 GTTGGTCCAAAAATATTAGATGCCATCCTATTAGGCCTGCTGGAAGGAGTAGCTTCTTCTGGACT GTTGGTCCAAAAATATTAGATGCCATCCTATT_GGCCTGCTGGAAGGAGTAGCTTCTTCTGGACT CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1685398..1685525 26863196 MeRIP-seq:(Medium) rs1300018344 Functional Loss DEL dbSNP153 33..33 33 - - - 72785 RMVar_ID_72785 Human_SNP_ID_591025391 m1A Human chr16 + 1685563 1685563 1685563 ATATTTTTGGACCAACAGAAGAACCTCAGAACATACCCAAGAGGACAAATCCCCCAGGTATGGGC ATATTTTTGGACCAACAGAAGAACCTCAGAACGTACCCAAGAGGACAAATCCCCCAGGTATGGGC A G AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1685512..1691867 32194978 MeRIP-seq:(Medium) rs909750885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891136,Human_RBP_ID_1003046,Human_RBP_ID_1512966,Human_RBP_ID_1838585,Human_RBP_ID_3491885,Human_RBP_ID_5113794,Human_RBP_ID_6496138,Human_RBP_ID_9372041,Human_RBP_ID_12677011,Human_RBP_ID_17652540,Human_RBP_ID_17872292,Human_RBP_ID_18529642,Human_RBP_ID_19070458,Human_RBP_ID_22048556,Human_RBP_ID_26328026,Human_RBP_ID_26445605,Human_RBP_ID_27439373 Human_Splice_Rec_1659983,Human_Splice_Rec_1659993,Human_Splice_Rec_1659999,Human_Splice_Rec_1660007,Human_Splice_Rec_1660013,Human_Splice_Rec_1660023,Human_Splice_Rec_1660031,Human_Splice_Rec_1660043,Human_Splice_Rec_1660053,Human_Splice_Rec_1660059,Human_Splice_Rec_1660067,Human_Splice_Rec_1660073,Human_Splice_Rec_1660079,Human_Splice_Rec_1660083 Human_miRNA_ID_1191895,Human_miRNA_ID_1191896,Human_miRNA_ID_2255325,Human_miRNA_ID_2571117,Human_miRNA_ID_3044853 RMVar_hsa_circ_175534,RMVar_hsa_circ_295159,RMVar_hsa_circ_291871,RMVar_hsa_circ_36676,RMVar_hsa_circ_356801,RMVar_hsa_circ_357002,RMVar_hsa_circ_283954 72786 RMVar_ID_72786 Human_SNP_ID_591029072 m1A Human chr16 + 1699379 1699379 1699379 AACCAAAACAGCCTGTCCACTGCTGCTGTGGGATGGAGGAGGCGTAAGCAGAAACACTAACAGTA AACCAAAACAGCCTGTCCACTGCTGCTGTGGGTTGGAGGAGGCGTAAGCAGAAACACTAACAGTA A T JPT2 Ensembl:ENSG00000206053 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1699328..1699399 26863196 MeRIP-seq:(Medium) rs1392745388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5088,Human_RBP_ID_469001,Human_RBP_ID_1003061,Human_RBP_ID_1177150,Human_RBP_ID_1281093,Human_RBP_ID_1512991,Human_RBP_ID_1838615,Human_RBP_ID_3491904,Human_RBP_ID_4352533,Human_RBP_ID_6496204,Human_RBP_ID_8186754,Human_RBP_ID_9285530,Human_RBP_ID_12677315,Human_RBP_ID_17255815,Human_RBP_ID_17368735,Human_RBP_ID_17872315,Human_RBP_ID_22581687,Human_RBP_ID_23680328,Human_RBP_ID_26439397,Human_RBP_ID_27237522 Human_miRNA_ID_265068 RMVar_hsa_circ_175538 72787 RMVar_ID_72787 Human_SNP_ID_591039581 m1A Human chr16 - 1735452 1735448 1735452 ACGGTCACACTCTCACACGGACGCTCACACGGACGGTCACACGGATGCTCACACGGATGGTCACA ACGGTCACACTCTCACACGGACGCTCACACGG____TCACACGGATGCTCACACGGATGGTCACA ACCGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1735444..1735605 26863196 MeRIP-seq:(Medium) rs1237116537 Functional Loss DEL dbSNP153 33..36 33 - - - 72788 RMVar_ID_72788 Human_SNP_ID_591039596 m1A Human chr16 - 1735468 1735466 1735468 ACGGACGCTCACATGGACGGTCACACTCTCACACGGACGCTCACACGGACGGTCACACGGATGCT ACGGACGCTCACATGGACGGTCACACTCTCAC__GGACGCTCACACGGACGGTCACACGGATGCT CGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1735393..1735626 26863196 MeRIP-seq:(Medium) rs1243975245 Functional Loss DEL dbSNP153 33..34 33 - - - 72789 RMVar_ID_72789 Human_SNP_ID_591040447 m1A Human chr16 - 1736585 1736583 1736585 ACGGTCACACGGATGCTCACATGGATGGTCACACGCTCACACGGACGGTCACACACGGACAGTCA ACGGTCACACGGATGCTCACATGGATGGTCAC__GCTCACACGGACGGTCACACACGGACAGTCA CGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1736577..1736718 26863196 MeRIP-seq:(Medium) rs537709654 Functional Loss DEL dbSNP153 33..34 33 - - - 72790 RMVar_ID_72790 Human_SNP_ID_591040452 m1A Human chr16 - 1736585 1736585 1736585 ACGGTCACACGGATGCTCACATGGATGGTCACACGCTCACACGGACGGTCACACACGGACAGTCA ACGGTCACACGGATGCTCACATGGATGGTCACTCGCTCACACGGACGGTCACACACGGACAGTCA T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1736577..1736718 26863196 MeRIP-seq:(Medium) rs1346392626 Functional Loss SNV dbSNP153 33..33 33 - - - 72791 RMVar_ID_72791 Human_SNP_ID_591040515 m1A Human chr16 - 1736681 1736677 1736681 TCACACGGACGCTCACACGGTCGGTCACACGGATGCTCACACGGACGGTCACACGCTCACACGGA TCACACGGACGCTCACACGGTCGGTCACACGG____TCACACGGACGGTCACACGCTCACACGGA AGCAT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1736673..1736806 26863196 MeRIP-seq:(Medium) rs1276397731 Functional Loss DEL dbSNP153 33..36 33 - - - 72792 RMVar_ID_72792 Human_SNP_ID_591040517 m1A Human chr16 - 1736681 1736678 1736682 TCACACGGACGCTCACACGGTCGGTCACACGGATGCTCACACGGACGGTCACACGCTCACACGGA TCACACGGACGCTCACACGGTCGGTCACACG____CTCACACGGACGGTCACACGCTCACACGGA GCATC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1736673..1736806 26863196 MeRIP-seq:(Medium) rs1476006008 Functional Loss DEL dbSNP153 32..35 33 - - - 72793 RMVar_ID_72793 Human_SNP_ID_591040775 m1A Human chr16 - 1736955 1736953 1736955 ATGCTCACACGGACGGTCACACGGACGGTCACACGCTCACATGGACGGTCACGGATGCTCACATG ATGCTCACACGGACGGTCACACGGACGGTCAC__GCTCACATGGACGGTCACGGATGCTCACATG CGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1736950..1737024 26863196 MeRIP-seq:(Medium) rs1334413961 Functional Loss DEL dbSNP153 33..34 33 - - - 72794 RMVar_ID_72794 Human_SNP_ID_591041096 m1A Human chr16 - 1737353 1737351 1737353 GGTCACACTCTCACACGGACGGTCACACACTCACGGACGGTCACGCTCACACGGATGCTCACACG GGTCACACTCTCACACGGACGGTCACACACTC__GGACGGTCACGCTCACACGGATGCTCACACG CGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1737345..1737420 26863196 MeRIP-seq:(Medium) rs1340915047 Functional Loss DEL dbSNP153 33..34 33 - - - 72795 RMVar_ID_72795 Human_SNP_ID_591041324 m1A Human chr16 + 1737647 1737647 1737647 TGTGTGTGACCATCCATGTGAGCATCCGTGTGACTGTCCGTGTGAGCGTCCGTGTGAGCGTGTGA TGTGTGTGACCATCCATGTGAGCATCCGTGTGTCTGTCCGTGTGAGCGTCCGTGTGAGCGTGTGA A T MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1737640..1737725 26863410 MeRIP-seq:(Medium) rs1420698530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23680671 RMVar_hsa_circ_29106,RMVar_hsa_circ_119620,RMVar_hsa_circ_175539,RMVar_hsa_circ_28036 72796 RMVar_ID_72796 Human_SNP_ID_591042113 m1A Human chr16 + 1738660 1738642 1738660 GTGAGCGTGTGAGCGTCCGTGTGAGTGTGACCATCCATGTGAGCATGTGTGACCGTCCGTGTAGC GTGAGCGTGTGAGCG__________________TCCATGTGAGCATGTGTGACCGTCCGTGTAGC GTCCGTGTGAGTGTGACCA G MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1738409..1738722 26863196 MeRIP-seq:(Medium) rs1567170508 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_5646704,Human_RBP_ID_17256228,Human_RBP_ID_23680729 RMVar_hsa_circ_29106,RMVar_hsa_circ_119620,RMVar_hsa_circ_175539,RMVar_hsa_circ_28036 72797 RMVar_ID_72797 Human_SNP_ID_591042129 m1A Human chr16 + 1738660 1738660 1738660 GTGAGCGTGTGAGCGTCCGTGTGAGTGTGACCATCCATGTGAGCATGTGTGACCGTCCGTGTAGC GTGAGCGTGTGAGCGTCCGTGTGAGTGTGACCCTCCATGTGAGCATGTGTGACCGTCCGTGTAGC A C MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1738409..1738722 26863196 MeRIP-seq:(Medium) rs1174912060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5646704,Human_RBP_ID_17256228,Human_RBP_ID_23680729 RMVar_hsa_circ_29106,RMVar_hsa_circ_119620,RMVar_hsa_circ_175539,RMVar_hsa_circ_28036 72798 RMVar_ID_72798 Human_SNP_ID_591042149 m1A Human chr16 - 1738694 1738694 1738694 ACACTCACACGGATGCTCACACGCTCACATGGATGCTACACGGACGGTCACACATGCTCACATGG ACACTCACACGGATGCTCACACGCTCACATGGCTGCTACACGGACGGTCACACATGCTCACATGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1738680..1738778 26863196 MeRIP-seq:(Medium) rs1431847475 Functional Loss SNV dbSNP153 33..33 33 - - - 72799 RMVar_ID_72799 Human_SNP_ID_591042783 m1A Human chr16 - 1739451 1739447 1739451 TCACACGGACGGTCACACGGAAGCTCACACGGACGGTCACACGGAGGCTCACACGGACGGTCACA TCACACGGACGGTCACACGGAAGCTCACACGG____TCACACGGAGGCTCACACGGACGGTCACA ACCGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1739445..1739720 26863196 MeRIP-seq:(Medium) rs1385650060 Functional Loss DEL dbSNP153 33..36 33 - - - 72800 RMVar_ID_72800 Human_SNP_ID_591044297 m1A Human chr16 - 1743416 1743416 1743416 CCGAGGTCACTCAGGTGCCAGTGGTCCCCCGCAGGCACGAGCTTGCCCCCGATCTGTGCACGTAC CCGAGGTCACTCAGGTGCCAGTGGTCCCCCGCGGGCACGAGCTTGCCCCCGATCTGTGCACGTAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1743371..1743571 32194978 MeRIP-seq:(Medium) rs769519320 Functional Loss SNV dbSNP153 33..33 33 - - - 72801 RMVar_ID_72801 Human_SNP_ID_591051706 m1A Human chr16 + 1766223 1766223 1766223 CCAGCCCAAGCTCACCTCTCCTAACACAGGGGAGGTGGCCACCATCGCCAACGGGAAGGTCAACC CCAGCCCAAGCTCACCTCTCCTAACACAGGGGTGGTGGCCACCATCGCCAACGGGAAGGTCAACC A T MAPK8IP3 Ensembl:ENSG00000138834 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1766219..1766321 26863196 MeRIP-seq:(Medium) rs1413994254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5523876,Human_RBP_ID_8231773,Human_RBP_ID_9372054,Human_RBP_ID_18469623,Human_RBP_ID_18985059 Human_Splice_Rec_1660134,Human_Splice_Rec_1660194,Human_Splice_Rec_1660252,Human_Splice_Rec_1660312 RMVar_hsa_circ_39015,RMVar_hsa_circ_319555,RMVar_hsa_circ_175547 72802 RMVar_ID_72802 Human_SNP_ID_591052985 m1A Human chr16 - 1768763 1768763 1768763 CGATGATGTGACTGCGCTCTGCCTTGGACAGCACGGGCTTCACCTGGCTCATGTCCCCTGCGCCC CGATGATGTGACTGCGCTCTGCCTTGGACAGCCCGGGCTTCACCTGGCTCATGTCCCCTGCGCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1768642..1768912 26863196 MeRIP-seq:(Medium) rs759454003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513122 72803 RMVar_ID_72803 Human_SNP_ID_591053549 m1A Human chr16 + 1770024 1770024 1770024 TGCACTCCTGTCTGGGAGGCCCTTATGAGGGCAGCCCAGCCCCCGCACCCACCCCCAACCAGAGA TGCACTCCTGTCTGGGAGGCCCTTATGAGGGCGGCCCAGCCCCCGCACCCACCCCCAACCAGAGA A G MAPK8IP3 Ensembl:ENSG00000138834 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1769887..1770169 26863196 MeRIP-seq:(Medium) rs924396089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5524803 Human_miRNA_ID_1157629,Human_miRNA_ID_1357140 72804 RMVar_ID_72804 Human_SNP_ID_591054356 m1A Human chr16 - 1771265 1771246 1771265 GCGCTGAAGCTGGTGCAGGTGGGGGCGCGGTGAGCGAGCGGGGGCGCGGTGTGGGGGGAAGGGGA GCGCTGAAGCTGGTGCAGGTGGGGGCGCGGTG___________________TGGGGGGAAGGGGA ACACCGCGCCCCCGCTCGCT A NME3 Ensembl:ENSG00000103024 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1771172..1771449 26863196 MeRIP-seq:(Medium) rs777708137 Functional Loss DEL dbSNP153 33..51 33 - - - 72805 RMVar_ID_72805 Human_SNP_ID_591054372 m1A Human chr16 - 1771265 1771265 1771265 GCGCTGAAGCTGGTGCAGGTGGGGGCGCGGTGAGCGAGCGGGGGCGCGGTGTGGGGGGAAGGGGA GCGCTGAAGCTGGTGCAGGTGGGGGCGCGGTGGGCGAGCGGGGGCGCGGTGTGGGGGGAAGGGGA T C NME3 Ensembl:ENSG00000103024 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1771172..1771449 26863196 MeRIP-seq:(Medium) rs1448054423 Functional Loss SNV dbSNP153 33..33 33 - - - 72806 RMVar_ID_72806 Human_SNP_ID_591054398 m1A Human chr16 - 1771305 1771305 1771305 GATTGTGCGGCGCTTCGAGAGGAAGGGCTTCAAGTTGGTGGCGCTGAAGCTGGTGCAGGTGGGGG GATTGTGCGGCGCTTCGAGAGGAAGGGCTTCAGGTTGGTGGCGCTGAAGCTGGTGCAGGTGGGGG T C NME3 Ensembl:ENSG00000103024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:1770876..1771575;chr16:1770901..1771550 26863196 MeRIP-seq:(Medium) rs202165010 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_46074,Human_RBP_ID_1513138,Human_RBP_ID_4352730,Human_RBP_ID_23680933 Human_Splice_Rec_1660419,Human_Splice_Rec_1660427,Human_Splice_Rec_1660441,Human_Splice_Rec_1660447,Human_Splice_Rec_1660467 72807 RMVar_ID_72807 Human_SNP_ID_591054457 m1A Human chr16 - 1771405 1771405 1771405 GACGGCCCGTCCCCGCCTGCCCCGCAGCCTGCACCGGCGCACACGAACGCACCTTCCTGGCCGTG GACGGCCCGTCCCCGCCTGCCCCGCAGCCTGCCCCGGCGCACACGAACGCACCTTCCTGGCCGTG T G NME3 Ensembl:ENSG00000103024 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1771301..1771680 26863410 MeRIP-seq:(Medium) rs77638350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1660418,Human_Splice_Rec_1660426,Human_Splice_Rec_1660440,Human_Splice_Rec_1660454,Human_Splice_Rec_1660460,Human_Splice_Rec_1660466 72808 RMVar_ID_72808 Human_SNP_ID_591054515 m1A Human chr16 + 1771500 1771500 1771500 GGCCCGCGCCGCGCGGCTCACCCGCGGGGAAGAGGTTAGCGAAGATGGTCAGCACCAGGCAGATC GGCCCGCGCCGCGCGGCTCACCCGCGGGGAAGCGGTTAGCGAAGATGGTCAGCACCAGGCAGATC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:1771200..1771525 26863196 MeRIP-seq:(Medium) rs1247153655 Functional Loss SNV dbSNP153 33..33 33 - - - 72809 RMVar_ID_72809 Human_SNP_ID_591054827 m1A Human chr16 + 1772091 1772091 1772091 CCCCAGCCCTCCCCCCTAAGATGCAGACCCTCAGAACACGTCGCGGAAGGTGAGCTCCCTGCTCC CCCCAGCCCTCCCCCCTAAGATGCAGACCCTCGGAACACGTCGCGGAAGGTGAGCTCCCTGCTCC A G NONHSAG018276.2 RNACentral:URS00008C25BF lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1772076..1772100 26863196 MeRIP-seq:(Medium) rs1398075749 Functional Loss SNV dbSNP153 33..33 33 - - - 72810 RMVar_ID_72810 Human_SNP_ID_591054986 m1A Human chr16 - 1772336 1772336 1772336 CCGGGCCATGATTATCGCAGAACGACAGAAAAATGGAGACACAAGCACCGAGGAGCCCATGCTGA CCGGGCCATGATTATCGCAGAACGACAGAAAAGTGGAGACACAAGCACCGAGGAGCCCATGCTGA T C MRPS34 Ensembl:ENSG00000074071 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:1772226..1772475 26863196 MeRIP-seq:(Medium) rs1280008747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513148,Human_RBP_ID_1838686,Human_RBP_ID_9372056,Human_RBP_ID_12677917,Human_RBP_ID_18673985,Human_RBP_ID_26328453 72811 RMVar_ID_72811 Human_SNP_ID_591054987 m1A Human chr16 - 1772342 1772342 1772342 TCTCCTCCGGGCCATGATTATCGCAGAACGACAGAAAAATGGAGACACAAGCACCGAGGAGCCCA TCTCCTCCGGGCCATGATTATCGCAGAACGACGGAAAAATGGAGACACAAGCACCGAGGAGCCCA T C MRPS34 Ensembl:ENSG00000074071 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1772056..1772495 26863196 MeRIP-seq:(Medium) rs1446893960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513148,Human_RBP_ID_1838686,Human_RBP_ID_12677917,Human_RBP_ID_23680946,Human_RBP_ID_26328453 72812 RMVar_ID_72812 Human_SNP_ID_591054988 m1A Human chr16 - 1772342 1772342 1772342 TCTCCTCCGGGCCATGATTATCGCAGAACGACAGAAAAATGGAGACACAAGCACCGAGGAGCCCA TCTCCTCCGGGCCATGATTATCGCAGAACGACCGAAAAATGGAGACACAAGCACCGAGGAGCCCA T G MRPS34 Ensembl:ENSG00000074071 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1772056..1772495 26863196 MeRIP-seq:(Medium) rs1446893960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513148,Human_RBP_ID_1838686,Human_RBP_ID_12677917,Human_RBP_ID_23680946,Human_RBP_ID_26328453 72813 RMVar_ID_72813 Human_SNP_ID_591054996 m1A Human chr16 + 1772354 1772354 1772354 TGCTTGTGTCTCCATTTTTCTGTCGTTCTGCGATAATCATGGCCCGGAGGAGAGGCGGGTACGGC TGCTTGTGTCTCCATTTTTCTGTCGTTCTGCGGTAATCATGGCCCGGAGGAGAGGCGGGTACGGC A G NONHSAG018276.2 RNACentral:URS00008C25BF lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1771876..1772536 26863196 MeRIP-seq:(Medium) rs1192698087 Functional Loss SNV dbSNP153 33..33 33 - - - 72814 RMVar_ID_72814 Human_SNP_ID_591055010 m1A Human chr16 + 1772372 1772372 1772372 TCTGTCGTTCTGCGATAATCATGGCCCGGAGGAGAGGCGGGTACGGCACGGAGGCCAGGCTGTCT TCTGTCGTTCTGCGATAATCATGGCCCGGAGGCGAGGCGGGTACGGCACGGAGGCCAGGCTGTCT A C NONHSAG018276.2 RNACentral:URS00008C25BF lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:1772326..1772375 26863196 MeRIP-seq:(Medium) rs773166124 Functional Loss SNV dbSNP153 33..33 33 - - - 72815 RMVar_ID_72815 Human_SNP_ID_591055455 m1A Human chr16 + 1773099 1773099 1773099 ACGCGGCGGGCCAGCTCCGCGATCAGCCGCGGACGCACCTTCTTCCGCGCCATGGCGGGTCCGCG ACGCGGCGGGCCAGCTCCGCGATCAGCCGCGGCCGCACCTTCTTCCGCGCCATGGCGGGTCCGCG A C EME2 Ensembl:ENSG00000197774 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:1773076..1773100;chr16:1772883..1773150 26863196 MeRIP-seq:(Medium) rs960799129 Functional Loss SNV dbSNP153 33..33 33 - - - 72816 RMVar_ID_72816 Human_SNP_ID_591055681 m1A Human chr16 - 1773445 1773445 1773445 CACCTGTGTCCACGCACACCGCGAGGCGCTTCAGGACCTGCTCCGGCCGCAGCAGCCGCAACGCC CACCTGTGTCCACGCACACCGCGAGGCGCTTCGGGACCTGCTCCGGCCGCAGCAGCCGCAACGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1773394..1773488 26863196 MeRIP-seq:(Medium) rs1322995443 Functional Loss SNV dbSNP153 33..33 33 - - - 72817 RMVar_ID_72817 Human_SNP_ID_591057327 m1A Human chr16 + 1776243 1776243 1776243 TGATCTCCTGCTGGACCTGGGCTCCTGACCACACGTGGGACCACCAGGACAGCATGCAGCCTTGG TGATCTCCTGCTGGACCTGGGCTCCTGACCACGCGTGGGACCACCAGGACAGCATGCAGCCTTGG A G EME2 Ensembl:ENSG00000197774 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1776234..1776317 26863196 MeRIP-seq:(Medium) rs777350603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234289,Human_RBP_ID_817248,Human_RBP_ID_8428584,Human_RBP_ID_9372058,Human_RBP_ID_17872398,Human_RBP_ID_18985082 Human_Splice_Rec_1660527,Human_Splice_Rec_1660533 RMVar_hsa_circ_114938,RMVar_hsa_circ_121847,RMVar_hsa_circ_175550,RMVar_hsa_circ_175551 72818 RMVar_ID_72818 Human_SNP_ID_591058751 m1A Human chr16 + 1779051 1779051 1779051 CAGGGCAGTCCCCACCACACTGTGGCCCAACGACCTTCCTGTTACCTGAGCAGACCTGGCTCACC CAGGGCAGTCCCCACCACACTGTGGCCCAACGGCCTTCCTGTTACCTGAGCAGACCTGGCTCACC A G EME2 Ensembl:ENSG00000197774 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1779045..1779243 26863196 MeRIP-seq:(Medium) rs577986637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513195,Human_RBP_ID_5128435,Human_RBP_ID_12677949 72819 RMVar_ID_72819 Human_SNP_ID_591058755 m1A Human chr16 - 1779060 1779060 1779060 GGACCCTGTGGTGAGCCAGGTCTGCTCAGGTAACAGGAAGGTCGTTGGGCCACAGTGTGGTGGGG GGACCCTGTGGTGAGCCAGGTCTGCTCAGGTAGCAGGAAGGTCGTTGGGCCACAGTGTGGTGGGG T C SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1779058..1779459 26863196 MeRIP-seq:(Medium) rs550852805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100006,RMVar_hsa_circ_175555 72820 RMVar_ID_72820 Human_SNP_ID_591059695 m1A Human chr16 + 1781493 1781493 1781493 CTGTTCCGGGGGCGTCTGGCCATGGTGGAAAGAATCTAGAAGAAAACACAGGCTCTGGGCAAAGG CTGTTCCGGGGGCGTCTGGCCATGGTGGAAAGGATCTAGAAGAAAACACAGGCTCTGGGCAAAGG A G EME2 Ensembl:ENSG00000197774 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1781314..1781500 26863196 MeRIP-seq:(Medium) rs971971682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18674031 72821 RMVar_ID_72821 Human_SNP_ID_591059696 m1A Human chr16 - 1781495 1781495 1781495 TTCCTTTGCCCAGAGCCTGTGTTTTCTTCTAGATTCTTTCCACCATGGCCAGACGCCCCCGGAAC TTCCTTTGCCCAGAGCCTGTGTTTTCTTCTAGGTTCTTTCCACCATGGCCAGACGCCCCCGGAAC T C SPSB3 Ensembl:ENSG00000162032 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1781487..1782114 26863196 MeRIP-seq:(Medium) rs748676240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1660536,Human_Splice_Rec_1660548,Human_Splice_Rec_1660558,Human_Splice_Rec_1660564,Human_Splice_Rec_1660574,Human_Splice_Rec_1660600,Human_Splice_Rec_1660608,Human_Splice_Rec_1660616,Human_Splice_Rec_1660620,Human_Splice_Rec_1660624 RMVar_hsa_circ_100006,RMVar_hsa_circ_175555 72822 RMVar_ID_72822 Human_SNP_ID_591060326 m1A Human chr16 + 1783025 1783025 1783025 GCAGCCGCGAGCTCCTGGAGGCGGCGGGATGGAGGCGGCGGCCGGTGAGTGGCGGGCCAGGGTGC GCAGCCGCGAGCTCCTGGAGGCGGCGGGATGGGGGCGGCGGCCGGTGAGTGGCGGGCCAGGGTGC A G NUBP2 Ensembl:ENSG00000095906 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:1782976..1783100;chr16:1782976..1783108;chr16:1782976..1783103 26863196 MeRIP-seq:(Medium) rs1025220344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392752,Human_RBP_ID_5113804,Human_RBP_ID_9325745 Human_Splice_Rec_1660625,Human_Splice_Rec_1660629,Human_Splice_Rec_1660639,Human_Splice_Rec_1660647,Human_Splice_Rec_1660651,Human_Splice_Rec_1660663,Human_Splice_Rec_1660669,Human_Splice_Rec_1660683,Human_Splice_Rec_1660693,Human_Splice_Rec_1660703,Human_Splice_Rec_1660713 72823 RMVar_ID_72823 Human_SNP_ID_591060327 m1A Human chr16 + 1783025 1783025 1783025 GCAGCCGCGAGCTCCTGGAGGCGGCGGGATGGAGGCGGCGGCCGGTGAGTGGCGGGCCAGGGTGC GCAGCCGCGAGCTCCTGGAGGCGGCGGGATGGTGGCGGCGGCCGGTGAGTGGCGGGCCAGGGTGC A T NUBP2 Ensembl:ENSG00000095906 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:1782976..1783100;chr16:1782976..1783108;chr16:1782976..1783103 26863196 MeRIP-seq:(Medium) rs1025220344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392752,Human_RBP_ID_5113804,Human_RBP_ID_9325745 Human_Splice_Rec_1660625,Human_Splice_Rec_1660629,Human_Splice_Rec_1660639,Human_Splice_Rec_1660647,Human_Splice_Rec_1660651,Human_Splice_Rec_1660663,Human_Splice_Rec_1660669,Human_Splice_Rec_1660683,Human_Splice_Rec_1660693,Human_Splice_Rec_1660703,Human_Splice_Rec_1660713 72824 RMVar_ID_72824 Human_SNP_ID_591060335 m1A Human chr16 - 1783038 1783038 1783038 CTGGAGCGGCTCCGCACCCTGGCCCGCCACTCACCGGCCGCCGCCTCCATCCCGCCGCCTCCAGG CTGGAGCGGCTCCGCACCCTGGCCCGCCACTCCCCGGCCGCCGCCTCCATCCCGCCGCCTCCAGG T G SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr16:1783000..1783200;chr16:1782926..1783150 26863410,26863196 MeRIP-seq:(Medium) rs1334808667 Functional Loss SNV dbSNP153 33..33 33 - - - 72825 RMVar_ID_72825 Human_SNP_ID_591061767 m1A Human chr16 - 1786803 1786803 1786803 ACTGGTGCACAGCCCTGCCCTGCGCCCCGAGCATGCGGGGGATACTGGGGCCACACAGGTCCACA ACTGGTGCACAGCCCTGCCCTGCGCCCCGAGCCTGCGGGGGATACTGGGGCCACACAGGTCCACA T G SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1786796..1786979 26863196 MeRIP-seq:(Medium) rs149114461 Functional Loss SNV dbSNP153 33..33 33 - - - 72826 RMVar_ID_72826 Human_SNP_ID_591061798 m1A Human chr16 + 1786852 1786852 1786852 AGGGCTGTGCACCAGTGCGACCGCGGCTGGGCACCCGTCTTCCTGGACCGGGAGCAGAGCATCTC AGGGCTGTGCACCAGTGCGACCGCGGCTGGGCGCCCGTCTTCCTGGACCGGGAGCAGAGCATCTC A G NUBP2 Ensembl:ENSG00000095906 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1786801..1786900 26863196 MeRIP-seq:(Medium) rs994590470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760707,Human_RBP_ID_26768854 Human_Splice_Rec_1660650,Human_Splice_Rec_1660654,Human_Splice_Rec_1660674,Human_Splice_Rec_1660688,Human_Splice_Rec_1660716,Human_Splice_Rec_1660726,Human_Splice_Rec_1660732 RMVar_hsa_circ_115341,RMVar_hsa_circ_175557 72827 RMVar_ID_72827 Human_SNP_ID_591061970 m1A Human chr16 + 1787278 1787278 1787278 GGGGTTCTGGTGCCTCTGGAGCAGGTGGCATTAGACGCCCCCAAAGGCAGGGAGAGGCTGGTGGG GGGGTTCTGGTGCCTCTGGAGCAGGTGGCATTGGACGCCCCCAAAGGCAGGGAGAGGCTGGTGGG A G NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:1787275..1787525;chr16:1787275..1787476 26863196 MeRIP-seq:(Medium) rs558940533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22581695,Human_RBP_ID_22800001,Human_RBP_ID_23256628 RMVar_hsa_circ_115341,RMVar_hsa_circ_175557 72828 RMVar_ID_72828 Human_SNP_ID_591061971 m1A Human chr16 + 1787278 1787278 1787278 GGGGTTCTGGTGCCTCTGGAGCAGGTGGCATTAGACGCCCCCAAAGGCAGGGAGAGGCTGGTGGG GGGGTTCTGGTGCCTCTGGAGCAGGTGGCATTTGACGCCCCCAAAGGCAGGGAGAGGCTGGTGGG A T NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:1787275..1787525;chr16:1787275..1787476 26863196 MeRIP-seq:(Medium) rs558940533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22581695,Human_RBP_ID_22800001,Human_RBP_ID_23256628 RMVar_hsa_circ_115341,RMVar_hsa_circ_175557 72829 RMVar_ID_72829 Human_SNP_ID_591062174 m1A Human chr16 - 1787759 1787759 1787759 GGACGCAGGGCTTCTATGGTGGCCATGTGCTCATCGGAGGTCCCCGGGGGCGTGTCCACCACCAG GGACGCAGGGCTTCTATGGTGGCCATGTGCTCCTCGGAGGTCCCCGGGGGCGTGTCCACCACCAG T G SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1787751..1787775 26863196 MeRIP-seq:(Medium) rs1356594823 Functional Loss SNV dbSNP153 33..33 33 - - - 72830 RMVar_ID_72830 Human_SNP_ID_591062330 m1A Human chr16 + 1788010 1788010 1788010 TCTGTAGGAAGACGGGCTTGCGGGTGATGGGAATCGTGGAGAATATGAGCGGCTTCACCTGCCCA TCTGTAGGAAGACGGGCTTGCGGGTGATGGGAGTCGTGGAGAATATGAGCGGCTTCACCTGCCCA A G NUBP2 Ensembl:ENSG00000095906 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1787726..1788075 26863196 MeRIP-seq:(Medium) rs1252398131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469190,Human_RBP_ID_4353002,Human_RBP_ID_12678109,Human_RBP_ID_23680964,Human_RBP_ID_26444692 Human_Splice_Rec_1660634,Human_Splice_Rec_1660635,Human_Splice_Rec_1660642,Human_Splice_Rec_1660643,Human_Splice_Rec_1660658,Human_Splice_Rec_1660659,Human_Splice_Rec_1660678,Human_Splice_Rec_1660679,Human_Splice_Rec_1660692,Human_Splice_Rec_1660698,Human_Splice_Rec_1660699,Human_Splice_Rec_1660708,Human_Splice_Rec_1660709,Human_Splice_Rec_1660720,Human_Splice_Rec_1660736,Human_Splice_Rec_1660737,Human_Splice_Rec_1660744,Human_Splice_Rec_1660745 RMVar_hsa_circ_117286,RMVar_hsa_circ_115341,RMVar_hsa_circ_175557,RMVar_hsa_circ_175558 72831 RMVar_ID_72831 Human_SNP_ID_591062351 m1A Human chr16 + 1788049 1788049 1788049 AGAATATGAGCGGCTTCACCTGCCCACACTGCACGGTGAGTCCCGGGGGTTGCAGAGGGGGCGAG AGAATATGAGCGGCTTCACCTGCCCACACTGCGCGGTGAGTCCCGGGGGTTGCAGAGGGGGCGAG A G NUBP2 Ensembl:ENSG00000095906 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1788032..1788133 26863410 MeRIP-seq:(Medium) rs57822546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070498,Human_RBP_ID_26444692 Human_Splice_Rec_1660635,Human_Splice_Rec_1660643,Human_Splice_Rec_1660659,Human_Splice_Rec_1660679,Human_Splice_Rec_1660699,Human_Splice_Rec_1660709,Human_Splice_Rec_1660737,Human_Splice_Rec_1660745 RMVar_hsa_circ_117286,RMVar_hsa_circ_115341,RMVar_hsa_circ_175557,RMVar_hsa_circ_175558 72832 RMVar_ID_72832 Human_SNP_ID_591062352 m1A Human chr16 + 1788049 1788049 1788049 AGAATATGAGCGGCTTCACCTGCCCACACTGCACGGTGAGTCCCGGGGGTTGCAGAGGGGGCGAG AGAATATGAGCGGCTTCACCTGCCCACACTGCTCGGTGAGTCCCGGGGGTTGCAGAGGGGGCGAG A T NUBP2 Ensembl:ENSG00000095906 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1788032..1788133 26863410 MeRIP-seq:(Medium) rs57822546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070498,Human_RBP_ID_26444692 Human_Splice_Rec_1660635,Human_Splice_Rec_1660643,Human_Splice_Rec_1660659,Human_Splice_Rec_1660679,Human_Splice_Rec_1660699,Human_Splice_Rec_1660709,Human_Splice_Rec_1660737,Human_Splice_Rec_1660745 RMVar_hsa_circ_117286,RMVar_hsa_circ_115341,RMVar_hsa_circ_175557,RMVar_hsa_circ_175558 72833 RMVar_ID_72833 Human_SNP_ID_591062435 m1A Human chr16 - 1788187 1788187 1788187 TGGGACACTCACCTAAGAAGGGCACCCCGGCGAGCTGGGCCAGCTCCTCTCCGCCGCCCCTGGAG TGGGACACTCACCTAAGAAGGGCACCCCGGCGGGCTGGGCCAGCTCCTCTCCGCCGCCCCTGGAG T C SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:1788126..1788225 26863196 MeRIP-seq:(Medium) rs1355143394 Functional Loss SNV dbSNP153 33..33 33 - - - 72834 RMVar_ID_72834 Human_SNP_ID_591062729 m1A Human chr16 + 1788772 1788772 1788772 CAGGGCCACCAAGGGCTCTGCTCCAGCCTCTCAGAGAAACAGAGGCCTGGGCTCGGTTCCCGGGC CAGGGCCACCAAGGGCTCTGCTCCAGCCTCTCGGAGAAACAGAGGCCTGGGCTCGGTTCCCGGGC A G NUBP2 Ensembl:ENSG00000095906 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1788764..1788966 26863196 MeRIP-seq:(Medium) rs1481837810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113806,Human_RBP_ID_17652860 RMVar_hsa_circ_117286,RMVar_hsa_circ_115341,RMVar_hsa_circ_175557,RMVar_hsa_circ_81291,RMVar_hsa_circ_175558,RMVar_hsa_circ_175559 72835 RMVar_ID_72835 Human_SNP_ID_591071597 m1A Human chr16 + 1809257 1809249 1809257 GAAAGCCAGTTACCTAAAAGAGCCTAATCCCCAAATCCGCTGAAGGTGCAGGGCGGCCTCAGTCC GAAAGCCAGTTACCTAAAAGAGCCT________AATCCGCTGAAGGTGCAGGGCGGCCTCAGTCC TAATCCCCA T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1809168..1809268 26863410 MeRIP-seq:(Medium) rs757141804 Functional Loss DEL dbSNP153 26..33 33 - - - 72836 RMVar_ID_72836 Human_SNP_ID_591071604 m1A Human chr16 + 1809257 1809257 1809257 GAAAGCCAGTTACCTAAAAGAGCCTAATCCCCAAATCCGCTGAAGGTGCAGGGCGGCCTCAGTCC GAAAGCCAGTTACCTAAAAGAGCCTAATCCCCTAATCCGCTGAAGGTGCAGGGCGGCCTCAGTCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1809168..1809268 26863410 MeRIP-seq:(Medium) rs1426510604 Functional Loss SNV dbSNP153 33..33 33 - - - 72837 RMVar_ID_72837 Human_SNP_ID_591071666 m1A Human chr16 - 1809347 1809344 1809348 GAAGACGGTGCAGCAGCACGCAGGTGAGACGGACCCGGTGACCACCATGCGGGCCGTGCGCAGGG GAAGACGGTGCAGCAGCACGCAGGTGAGACG____CGGTGACCACCATGCGGGCCGTGCGCAGGG GGGTC G HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1809297..1809425 26863196 MeRIP-seq:(Medium) rs1567249668 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_17652863 Human_Splice_Rec_1660768,Human_Splice_Rec_1660774,Human_Splice_Rec_1660792,Human_Splice_Rec_1660806,Human_Splice_Rec_1660824,Human_Splice_Rec_1660828,Human_Splice_Rec_1660844 RMVar_hsa_circ_85120,RMVar_hsa_circ_267002,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_284292,RMVar_hsa_circ_175563 72838 RMVar_ID_72838 Human_SNP_ID_591071675 m1A Human chr16 - 1809351 1809351 1809351 GGGAGAAGACGGTGCAGCAGCACGCAGGTGAGACGGACCCGGTGACCACCATGCGGGCCGTGCGC GGGAGAAGACGGTGCAGCAGCACGCAGGTGAGTCGGACCCGGTGACCACCATGCGGGCCGTGCGC T A HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1809301..1809874 32194978 MeRIP-seq:(Medium) rs1418280261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17652863 Human_Splice_Rec_1660768,Human_Splice_Rec_1660774,Human_Splice_Rec_1660792,Human_Splice_Rec_1660806,Human_Splice_Rec_1660824,Human_Splice_Rec_1660828,Human_Splice_Rec_1660844 RMVar_hsa_circ_85120,RMVar_hsa_circ_267002,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_284292,RMVar_hsa_circ_175563 72839 RMVar_ID_72839 Human_SNP_ID_591071907 m1A Human chr16 - 1809759 1809759 1809759 GCAGAGGAGTTTACCTACAACCCCTTCATGAGAGTGAGGTGAGGCCCAGGGCAGGTGGTGGGCGC GCAGAGGAGTTTACCTACAACCCCTTCATGAGTGTGAGGTGAGGCCCAGGGCAGGTGGTGGGCGC T A HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1809751..1809850 26863196 MeRIP-seq:(Medium) rs754765416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5237535,Human_RBP_ID_17883986,Human_RBP_ID_18985092,Human_RBP_ID_19070501 Human_Splice_Rec_1660766,Human_Splice_Rec_1660767,Human_Splice_Rec_1660772,Human_Splice_Rec_1660773,Human_Splice_Rec_1660790,Human_Splice_Rec_1660791,Human_Splice_Rec_1660804,Human_Splice_Rec_1660805,Human_Splice_Rec_1660822,Human_Splice_Rec_1660823,Human_Splice_Rec_1660827,Human_Splice_Rec_1660842,Human_Splice_Rec_1660843 RMVar_hsa_circ_85120,RMVar_hsa_circ_267002,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_284292,RMVar_hsa_circ_269397,RMVar_hsa_circ_175563,RMVar_hsa_circ_329682 72840 RMVar_ID_72840 Human_SNP_ID_591074045 m1A Human chr16 + 1815474 1815474 1815474 GCATTTCCACACAATGGGCTACTCAGAAGCAAAGAGCGTGGCTGACCCTCACCAACATCAGCGGG GCATTTCCACACAATGGGCTACTCAGAAGCAAGGAGCGTGGCTGACCCTCACCAACATCAGCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1815472..1815705 26863196 MeRIP-seq:(Medium) rs1485326585 Functional Loss SNV dbSNP153 33..33 33 - - - 72841 RMVar_ID_72841 Human_SNP_ID_591074626 m1A Human chr16 - 1816996 1816996 1816996 GCCTTCCGAGCTCACCTGTCACCTCTCTCCTCAGAGAGTCTACTGTGGCCACGAGTACACCATCA GCCTTCCGAGCTCACCTGTCACCTCTCTCCTCGGAGAGTCTACTGTGGCCACGAGTACACCATCA T C HAGH Ensembl:ENSG00000063854 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1816976..1817000 32194978 MeRIP-seq:(Medium) rs1567256588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_327993,RMVar_hsa_circ_175565 72842 RMVar_ID_72842 Human_SNP_ID_591074769 m1A Human chr16 - 1817235 1817235 1817235 CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTATGAAGGGACTGCGGATGAGATGTGTAAAGCTC CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTTTGAAGGGACTGCGGATGAGATGTGTAAAGCTC T A HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1817226..1817250 26863196 MeRIP-seq:(Medium) rs144037672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815813,Human_RBP_ID_4353078,Human_RBP_ID_19070502,Human_RBP_ID_27811464 Human_Splice_Rec_1660762,Human_Splice_Rec_1660763,Human_Splice_Rec_1660786,Human_Splice_Rec_1660787,Human_Splice_Rec_1660800,Human_Splice_Rec_1660801,Human_Splice_Rec_1660818,Human_Splice_Rec_1660819,Human_Splice_Rec_1660838,Human_Splice_Rec_1660839,Human_Splice_Rec_1660854 Human_miRNA_ID_2195870,Human_miRNA_ID_2210678,Human_miRNA_ID_2534845,Human_miRNA_ID_2536577 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_327993,RMVar_hsa_circ_175565 72843 RMVar_ID_72843 Human_SNP_ID_591074770 m1A Human chr16 - 1817235 1817235 1817235 CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTATGAAGGGACTGCGGATGAGATGTGTAAAGCTC CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTGTGAAGGGACTGCGGATGAGATGTGTAAAGCTC T C HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1817226..1817250 26863196 MeRIP-seq:(Medium) rs144037672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815813,Human_RBP_ID_4353078,Human_RBP_ID_19070502,Human_RBP_ID_27811464 Human_Splice_Rec_1660762,Human_Splice_Rec_1660763,Human_Splice_Rec_1660786,Human_Splice_Rec_1660787,Human_Splice_Rec_1660800,Human_Splice_Rec_1660801,Human_Splice_Rec_1660818,Human_Splice_Rec_1660819,Human_Splice_Rec_1660838,Human_Splice_Rec_1660839,Human_Splice_Rec_1660854 Human_miRNA_ID_2195870,Human_miRNA_ID_2210678,Human_miRNA_ID_2534845,Human_miRNA_ID_2536577 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_327993,RMVar_hsa_circ_175565 72844 RMVar_ID_72844 Human_SNP_ID_591074771 m1A Human chr16 - 1817235 1817235 1817235 CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTATGAAGGGACTGCGGATGAGATGTGTAAAGCTC CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTCTGAAGGGACTGCGGATGAGATGTGTAAAGCTC T G HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1817226..1817250 26863196 MeRIP-seq:(Medium) rs144037672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815813,Human_RBP_ID_4353078,Human_RBP_ID_19070502,Human_RBP_ID_27811464 Human_Splice_Rec_1660762,Human_Splice_Rec_1660763,Human_Splice_Rec_1660786,Human_Splice_Rec_1660787,Human_Splice_Rec_1660800,Human_Splice_Rec_1660801,Human_Splice_Rec_1660818,Human_Splice_Rec_1660819,Human_Splice_Rec_1660838,Human_Splice_Rec_1660839,Human_Splice_Rec_1660854 Human_miRNA_ID_2195870,Human_miRNA_ID_2210678,Human_miRNA_ID_2534845,Human_miRNA_ID_2536577 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_327993,RMVar_hsa_circ_175565 72845 RMVar_ID_72845 Human_SNP_ID_591074900 m1A Human chr16 + 1817560 1817560 1817560 ATCCCACCAACTGTGGCTCTGAGACCCTCACAAATCCAGCCCTCTCCCCAAACACGCAGCAGCCC ATCCCACCAACTGTGGCTCTGAGACCCTCACATATCCAGCCCTCTCCCCAAACACGCAGCAGCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1817389..1817872 26863196 MeRIP-seq:(Medium) rs759877410 Functional Loss SNV dbSNP153 33..33 33 - - - 72846 RMVar_ID_72846 Human_SNP_ID_591075473 m1A Human chr16 - 1819103 1819103 1819103 AGCCCCCTGCCGTGTTCACAGGTGCGTGTTCGAGTGTGGGTGGGGGCGGGGGTTCTTCGTGAAGA AGCCCCCTGCCGTGTTCACAGGTGCGTGTTCGGGTGTGGGTGGGGGCGGGGGTTCTTCGTGAAGA T C HAGH Ensembl:ENSG00000063854 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1819101..1821582 32194978 MeRIP-seq:(Medium) rs7205570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070503 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_175565 72847 RMVar_ID_72847 Human_SNP_ID_591075474 m1A Human chr16 - 1819103 1819103 1819103 AGCCCCCTGCCGTGTTCACAGGTGCGTGTTCGAGTGTGGGTGGGGGCGGGGGTTCTTCGTGAAGA AGCCCCCTGCCGTGTTCACAGGTGCGTGTTCGCGTGTGGGTGGGGGCGGGGGTTCTTCGTGAAGA T G HAGH Ensembl:ENSG00000063854 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1819101..1821582 32194978 MeRIP-seq:(Medium) rs7205570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070503 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_175565 72848 RMVar_ID_72848 Human_SNP_ID_591075532 m1A Human chr16 + 1819202 1819202 1819202 GTGTCCTGAAGTGTGGCACGGGGTCGCCAGGCACTTGACGTTCAGAGACCCCACCTTCAACAAAG GTGTCCTGAAGTGTGGCACGGGGTCGCCAGGCCCTTGACGTTCAGAGACCCCACCTTCAACAAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1819151..1819225 26863196 MeRIP-seq:(Medium) rs1474273168 Functional Loss SNV dbSNP153 33..33 33 - - - 72849 RMVar_ID_72849 Human_SNP_ID_591076000 m1A Human chr16 - 1820302 1820302 1820302 CTGCACCAGGACAAGAAATCCACCCCCAGGCCACGCCCCAGACCCACTGCCCTAGGATGTGGGGG CTGCACCAGGACAAGAAATCCACCCCCAGGCCTCGCCCCAGACCCACTGCCCTAGGATGTGGGGG T A HAGH Ensembl:ENSG00000063854 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1820295..1820395 26863196 MeRIP-seq:(Medium) rs1208815796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85120,RMVar_hsa_circ_91024,RMVar_hsa_circ_175564,RMVar_hsa_circ_175560,RMVar_hsa_circ_107776,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_175565,RMVar_hsa_circ_175566,RMVar_hsa_circ_175567 72850 RMVar_ID_72850 Human_SNP_ID_591077060 m1A Human chr16 - 1822977 1822977 1822977 CACAGATTTGCGGAAGAACCTGACCGTGGACGAGGGCACCATGAAGGTAGAGGTGCTGCCTGCCC CACAGATTTGCGGAAGAACCTGACCGTGGACGGGGGCACCATGAAGGTAGAGGTGCTGCCTGCCC T C HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1822927..1826769 26863196 MeRIP-seq:(Medium) rs1002687580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760479,Human_RBP_ID_1838722,Human_RBP_ID_4393464,Human_RBP_ID_5571496,Human_RBP_ID_12678593,Human_RBP_ID_17883322 Human_Splice_Rec_1660778,Human_Splice_Rec_1660794,Human_Splice_Rec_1660810,Human_Splice_Rec_1660830,Human_Splice_Rec_1660846,Human_Splice_Rec_1660856,Human_Splice_Rec_1660864,Human_Splice_Rec_1660870,Human_Splice_Rec_1660876 Human_miRNA_ID_2195871 RMVar_hsa_circ_85120,RMVar_hsa_circ_91024,RMVar_hsa_circ_175564,RMVar_hsa_circ_175560,RMVar_hsa_circ_107776,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_175565,RMVar_hsa_circ_175566,RMVar_hsa_circ_175568,RMVar_hsa_circ_175567,RMVar_hsa_circ_277207,RMVar_hsa_circ_125905,RMVar_hsa_circ_175569 72851 RMVar_ID_72851 Human_SNP_ID_591077079 m1A Human chr16 + 1823001 1823001 1823001 TGGTGCCCTCGTCCACGGTCAGGTTCTTCCGCAAATCTGTGTGGCAGAAAACTCCCAGCAGGGCT TGGTGCCCTCGTCCACGGTCAGGTTCTTCCGCCAATCTGTGTGGCAGAAAACTCCCAGCAGGGCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1822278..1826597 32194978 MeRIP-seq:(Medium) rs749673184 Functional Loss SNV dbSNP153 33..33 33 - - - 72852 RMVar_ID_72852 Human_SNP_ID_591078686 m1A Human chr16 + 1827327 1827327 1827327 CGTGGGGAGGAACTACGCGGACCACGTCAGGGAGATGCGCAGCGCGGTGTTGAGCGAGCCCGTGC CGTGGGGAGGAACTACGCGGACCACGTCAGGGGGATGCGCAGCGCGGTGTTGAGCGAGCCCGTGC A G FAHD1 Ensembl:ENSG00000180185 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1827281..1827385 26863196 MeRIP-seq:(Medium) rs1229455100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762953,Human_RBP_ID_4353138,Human_RBP_ID_22441694 72853 RMVar_ID_72853 Human_SNP_ID_591095009 m1A Human chr16 - 1882187 1882187 1882187 AGCCTGGGCGACAGAGCGAGACTCGGTCTCAAAAAAAAAAAAAAAGAAAAGGAAAGAAAGAAATT AGCCTGGGCGACAGAGCGAGACTCGGTCTCAAGAAAAAAAAAAAAGAAAAGGAAAGAAAGAAATT T C LINC00254,MEIOB Ensembl:ENSG00000281219,Ensembl:ENSG00000162039 lincRNA,Protein coding intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:1882164..1882248 26863410 MeRIP-seq:(Medium) rs1321159626 Functional Loss SNV dbSNP153 33..33 33 - - - 72854 RMVar_ID_72854 Human_SNP_ID_591120506 m1A Human chr16 + 1959600 1959568 1959601 ACGGAGGTAGAGGCCAGGGCAGCGCGTCCGGGAGCGGAGTCCGCGCCCGCCGCCGCCATGCCGGA A_________________________________CGGAGTCCGCGCCCGCCGCCGCCATGCCGGA ACGGAGGTAGAGGCCAGGGCAGCGCGTCCGGGAG A NDUFB10 Ensembl:ENSG00000140990 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA Glucose starvation 4h chr16:1959526..1959812 31548705,26863196 m1A-IP-seq:(High) rs1355364324 Functional Loss DEL dbSNP153 2..34 33 - - - Human_RBP_ID_469836,Human_RBP_ID_4354444,Human_RBP_ID_5316485,Human_RBP_ID_5465792,Human_RBP_ID_9324823,Human_RBP_ID_22441212,Human_RBP_ID_22800055,Human_RBP_ID_26328027,Human_RBP_ID_26939597 RMVar_hsa_circ_91180,RMVar_hsa_circ_175581 72855 RMVar_ID_72855 Human_SNP_ID_591120531 m1A Human chr16 + 1959600 1959600 1959600 ACGGAGGTAGAGGCCAGGGCAGCGCGTCCGGGAGCGGAGTCCGCGCCCGCCGCCGCCATGCCGGA ACGGAGGTAGAGGCCAGGGCAGCGCGTCCGGGGGCGGAGTCCGCGCCCGCCGCCGCCATGCCGGA A G NDUFB10 Ensembl:ENSG00000140990 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA Glucose starvation 4h chr16:1959526..1959812 31548705,26863196 m1A-IP-seq:(High) rs1472505663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469836,Human_RBP_ID_4354444,Human_RBP_ID_5316485,Human_RBP_ID_5465792,Human_RBP_ID_9324823,Human_RBP_ID_22441212,Human_RBP_ID_22800055,Human_RBP_ID_26328027,Human_RBP_ID_26939597 RMVar_hsa_circ_91180,RMVar_hsa_circ_175581 72856 RMVar_ID_72856 Human_SNP_ID_591120566 m1A Human chr16 + 1959659 1959659 1959659 GCCGGACAGCTGGGACAAGGATGTGTACCCTGAGCCCCCGCGCCGCACGCCGGTGCAGCCCAATC GCCGGACAGCTGGGACAAGGATGTGTACCCTGGGCCCCCGCGCCGCACGCCGGTGCAGCCCAATC A G NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1959526..1959775 26863410 MeRIP-seq:(Medium) rs1254392358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233772,Human_RBP_ID_469838,Human_RBP_ID_1003270,Human_RBP_ID_1513584,Human_RBP_ID_3492278,Human_RBP_ID_4354444,Human_RBP_ID_5464749,Human_RBP_ID_8428972,Human_RBP_ID_9284400,Human_RBP_ID_12682990,Human_RBP_ID_17689772,Human_RBP_ID_18674407,Human_RBP_ID_22441695,Human_RBP_ID_22800056,Human_RBP_ID_23681805,Human_RBP_ID_26328027,Human_RBP_ID_26939598,Human_RBP_ID_27237988 Human_Splice_Rec_1661051,Human_Splice_Rec_1661057,Human_Splice_Rec_1661061,Human_Splice_Rec_1661063,Human_Splice_Rec_1661069 Human_miRNA_ID_2250235,Human_miRNA_ID_2269991 RMVar_hsa_circ_91180,RMVar_hsa_circ_175581 72857 RMVar_ID_72857 Human_SNP_ID_591120582 m1A Human chr16 + 1959689 1959689 1959689 TGAGCCCCCGCGCCGCACGCCGGTGCAGCCCAATCCCATCGTCTACATGATGAAAGCGTTCGACC TGAGCCCCCGCGCCGCACGCCGGTGCAGCCCAGTCCCATCGTCTACATGATGAAAGCGTTCGACC A G NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:1959587..1959702 26863410 MeRIP-seq:(Medium) rs368803523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233772,Human_RBP_ID_469840,Human_RBP_ID_817936,Human_RBP_ID_1513587,Human_RBP_ID_1839092,Human_RBP_ID_4354445,Human_RBP_ID_12682991,Human_RBP_ID_18437218,Human_RBP_ID_26939599,Human_RBP_ID_27439751 Human_Splice_Rec_1661051,Human_Splice_Rec_1661057,Human_Splice_Rec_1661061,Human_Splice_Rec_1661063,Human_Splice_Rec_1661069 RMVar_hsa_circ_91180,RMVar_hsa_circ_175581 72858 RMVar_ID_72858 Human_SNP_ID_591120599 m1A Human chr16 - 1959722 1959722 1959722 CTCTCACGAGGGTCACGGGTCGGTCCACGATGAGGTCGAACGCTTTCATCATGTAGACGATGGGA CTCTCACGAGGGTCACGGGTCGGTCCACGATGGGGTCGAACGCTTTCATCATGTAGACGATGGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1959604..1961300 32194978 MeRIP-seq:(Medium) rs751969932 Functional Loss SNV dbSNP153 33..33 33 - - - 72859 RMVar_ID_72859 Human_SNP_ID_591121165 m1A Human chr16 - 1961127 1961127 1961127 ATAAATTCTGCAAAGACAAAGCCACAGACTCAAATGCCTCATCGGTTTGGACAGGCTTTTAGCTT ATAAATTCTGCAAAGACAAAGCCACAGACTCACATGCCTCATCGGTTTGGACAGGCTTTTAGCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1961125..1961247 26863196 MeRIP-seq:(Medium) rs776188770 Functional Loss SNV dbSNP153 33..33 33 - - - 72860 RMVar_ID_72860 Human_SNP_ID_591121179 m1A Human chr16 - 1961157 1961156 1961158 TAATACCTGTTCTTTGCGTGCTGCCGCTCTATAAATTCTGCAAAGACAAAGCCACAGACTCAAAT TAATACCTGTTCTTTGCGTGCTGCCGCTCTA__AATTCTGCAAAGACAAAGCCACAGACTCAAAT TTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1961151..1961200 26863196 MeRIP-seq:(Medium) rs778962665 Functional Loss DEL dbSNP153 32..33 33 - - - 72861 RMVar_ID_72861 Human_SNP_ID_591121180 m1A Human chr16 - 1961156 1961156 1961156 AATACCTGTTCTTTGCGTGCTGCCGCTCTATAAATTCTGCAAAGACAAAGCCACAGACTCAAATG AATACCTGTTCTTTGCGTGCTGCCGCTCTATAGATTCTGCAAAGACAAAGCCACAGACTCAAATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1961151..1961175 26863196 MeRIP-seq:(Medium) rs1277711577 Functional Loss SNV dbSNP153 33..33 33 - - - 72862 RMVar_ID_72862 Human_SNP_ID_591121181 m1A Human chr16 - 1961156 1961156 1961156 AATACCTGTTCTTTGCGTGCTGCCGCTCTATAAATTCTGCAAAGACAAAGCCACAGACTCAAATG AATACCTGTTCTTTGCGTGCTGCCGCTCTATACATTCTGCAAAGACAAAGCCACAGACTCAAATG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1961151..1961175 26863196 MeRIP-seq:(Medium) rs1277711577 Functional Loss SNV dbSNP153 33..33 33 - - - 72863 RMVar_ID_72863 Human_SNP_ID_591121382 m1A Human chr16 + 1961553 1961553 1961553 CATTATGCAGGATCGGCTCAAAGCCTGTCAGCAGAGGGAAGGACAGAACTACCAGCAGAACTGTA CATTATGCAGGATCGGCTCAAAGCCTGTCAGCGGAGGGAAGGACAGAACTACCAGCAGAACTGTA A G NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1961467..1961875 26863196 MeRIP-seq:(Medium) rs374819190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513594,Human_RBP_ID_1839096,Human_RBP_ID_5180588,Human_RBP_ID_6498150,Human_RBP_ID_8428980,Human_RBP_ID_9372065,Human_RBP_ID_12683045,Human_RBP_ID_17652865,Human_RBP_ID_18674412,Human_RBP_ID_23681815,Human_RBP_ID_26328455,Human_RBP_ID_26809817,Human_RBP_ID_26939610 Human_Splice_Rec_1661054,Human_Splice_Rec_1661055,Human_Splice_Rec_1661060,Human_Splice_Rec_1661066,Human_Splice_Rec_1661067,Human_Splice_Rec_1661072,Human_Splice_Rec_1661073 Human_miRNA_ID_2949506,Human_miRNA_ID_2956189 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 72864 RMVar_ID_72864 Human_SNP_ID_591121420 m1A Human chr16 + 1961619 1961619 1961619 CAAGGAAGTGGAGCAGTTCACCCAGGTGGCCAAGGCCTACCAGGACCGCTGTGCGTGCCCCACCC CAAGGAAGTGGAGCAGTTCACCCAGGTGGCCACGGCCTACCAGGACCGCTGTGCGTGCCCCACCC A C NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1961476..1961635 32194978 MeRIP-seq:(Medium) rs748360281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469850,Human_RBP_ID_817937,Human_RBP_ID_890244,Human_RBP_ID_1513595,Human_RBP_ID_1839096,Human_RBP_ID_8428983,Human_RBP_ID_9372066,Human_RBP_ID_17652543,Human_RBP_ID_17872867,Human_RBP_ID_18674415,Human_RBP_ID_22441213,Human_RBP_ID_23681817 Human_Splice_Rec_1661055,Human_Splice_Rec_1661067 Human_miRNA_ID_1966329,Human_miRNA_ID_2218329,Human_miRNA_ID_2361786,Human_miRNA_ID_2675615,Human_miRNA_ID_2926366 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 72865 RMVar_ID_72865 Human_SNP_ID_591121421 m1A Human chr16 + 1961619 1961619 1961619 CAAGGAAGTGGAGCAGTTCACCCAGGTGGCCAAGGCCTACCAGGACCGCTGTGCGTGCCCCACCC CAAGGAAGTGGAGCAGTTCACCCAGGTGGCCAGGGCCTACCAGGACCGCTGTGCGTGCCCCACCC A G NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1961476..1961635 32194978 MeRIP-seq:(Medium) rs748360281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469850,Human_RBP_ID_817937,Human_RBP_ID_890244,Human_RBP_ID_1513595,Human_RBP_ID_1839096,Human_RBP_ID_8428983,Human_RBP_ID_9372066,Human_RBP_ID_17652543,Human_RBP_ID_17872867,Human_RBP_ID_18674415,Human_RBP_ID_22441213,Human_RBP_ID_23681817 Human_Splice_Rec_1661055,Human_Splice_Rec_1661067 Human_miRNA_ID_1966329,Human_miRNA_ID_2218329,Human_miRNA_ID_2361786,Human_miRNA_ID_2675615,Human_miRNA_ID_2926366 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 72866 RMVar_ID_72866 Human_SNP_ID_591121443 m1A Human chr16 + 1961648 1961647 1961648 CCAAGGCCTACCAGGACCGCTGTGCGTGCCCCACCCACCCCCAACCCCCCACCATCCTCCTGAGG CCAAGGCCTACCAGGACCGCTGTGCGTGCCCC_CCCACCCCCAACCCCCCACCATCCTCCTGAGG CA C NDUFB10 Ensembl:ENSG00000140990 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1444721256 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23681817 Human_miRNA_ID_1418542 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 72867 RMVar_ID_72867 Human_SNP_ID_591121445 m1A Human chr16 + 1961648 1961648 1961648 CCAAGGCCTACCAGGACCGCTGTGCGTGCCCCACCCACCCCCAACCCCCCACCATCCTCCTGAGG CCAAGGCCTACCAGGACCGCTGTGCGTGCCCCCCCCACCCCCAACCCCCCACCATCCTCCTGAGG A C NDUFB10 Ensembl:ENSG00000140990 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs762609751 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23681817 Human_miRNA_ID_1418542 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 72868 RMVar_ID_72868 Human_SNP_ID_591121614 m1A Human chr16 + 1961870 1961867 1961871 GCCAAACAGAGGCAGAGGATGCTGCAAGAGAGAAAAGCTGCAAAAGAGGCCGCCGCTGCCACCTC GCCAAACAGAGGCAGAGGATGCTGCAAGAG____AAGCTGCAAAAGAGGCCGCCGCTGCCACCTC GAGAA G NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1410162599 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_469856,Human_RBP_ID_1513601,Human_RBP_ID_4354472,Human_RBP_ID_17652868,Human_RBP_ID_17883328,Human_RBP_ID_23681820,Human_RBP_ID_26939612,Human_RBP_ID_27237998 Human_Splice_Rec_1661056,Human_Splice_Rec_1661068,Human_Splice_Rec_1661074 Human_miRNA_ID_2013431,Human_miRNA_ID_2759823 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_85293,RMVar_hsa_circ_175582,RMVar_hsa_circ_175583 72869 RMVar_ID_72869 Human_SNP_ID_591121785 m1A Human chr16 - 1962177 1962175 1962178 GGAGACTGTATTCACCAAGTCTCCCTATCAGGAGTTCACTGACCACCTCGTCAAGACCCACACCA GGAGACTGTATTCACCAAGTCTCCCTATCAG___TTCACTGACCACCTCGTCAAGACCCACACCA ACTC A RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1962126..1962225 32194978 MeRIP-seq:(Medium) rs1567316615 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_469861,Human_RBP_ID_894973,Human_RBP_ID_1003280,Human_RBP_ID_1088382,Human_RBP_ID_1365135,Human_RBP_ID_1513608,Human_RBP_ID_1839104,Human_RBP_ID_2469996,Human_RBP_ID_3492291,Human_RBP_ID_4396781,Human_RBP_ID_8428999,Human_RBP_ID_8805334,Human_RBP_ID_9060696,Human_RBP_ID_12683055,Human_RBP_ID_17256549,Human_RBP_ID_17488182,Human_RBP_ID_18189759,Human_RBP_ID_18674419,Human_RBP_ID_20101287,Human_RBP_ID_22497318,Human_RBP_ID_22800060,Human_RBP_ID_23681828,Human_RBP_ID_26439762,Human_RBP_ID_26809821,Human_RBP_ID_26939619,Human_RBP_ID_27238002,Human_RBP_ID_27439761 Human_Splice_Rec_1661086,Human_Splice_Rec_1661094,Human_Splice_Rec_1661104,Human_Splice_Rec_1661114,Human_Splice_Rec_1661122,Human_Splice_Rec_1661128,Human_Splice_Rec_1661134,Human_Splice_Rec_1661142,Human_Splice_Rec_1661152,Human_Splice_Rec_1661160,Human_Splice_Rec_1661168 RMVar_hsa_circ_84382,RMVar_hsa_circ_101397,RMVar_hsa_circ_116614,RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_95316,RMVar_hsa_circ_175587,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_175585,RMVar_hsa_circ_175586,RMVar_hsa_circ_175584 72870 RMVar_ID_72870 Human_SNP_ID_591121788 m1A Human chr16 - 1962183 1962183 1962183 CTGGAAGGAGACTGTATTCACCAAGTCTCCCTATCAGGAGTTCACTGACCACCTCGTCAAGACCC CTGGAAGGAGACTGTATTCACCAAGTCTCCCTTTCAGGAGTTCACTGACCACCTCGTCAAGACCC T A RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1962134..1962212 26863196 MeRIP-seq:(Medium) rs1437914020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469861,Human_RBP_ID_1365135,Human_RBP_ID_1513608,Human_RBP_ID_1839104,Human_RBP_ID_2469996,Human_RBP_ID_3492291,Human_RBP_ID_4396783,Human_RBP_ID_8429000,Human_RBP_ID_9060696,Human_RBP_ID_12683055,Human_RBP_ID_17256903,Human_RBP_ID_17488183,Human_RBP_ID_18189759,Human_RBP_ID_18674419,Human_RBP_ID_20101288,Human_RBP_ID_22936395,Human_RBP_ID_26809821,Human_RBP_ID_27439761 Human_Splice_Rec_1661086,Human_Splice_Rec_1661094,Human_Splice_Rec_1661104,Human_Splice_Rec_1661114,Human_Splice_Rec_1661122,Human_Splice_Rec_1661128,Human_Splice_Rec_1661134,Human_Splice_Rec_1661142,Human_Splice_Rec_1661152,Human_Splice_Rec_1661160,Human_Splice_Rec_1661168 RMVar_hsa_circ_84382,RMVar_hsa_circ_101397,RMVar_hsa_circ_116614,RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_95316,RMVar_hsa_circ_175587,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_175585,RMVar_hsa_circ_175586,RMVar_hsa_circ_175584 72871 RMVar_ID_72871 Human_SNP_ID_591121949 m1A Human chr16 - 1962458 1962458 1962458 GGTCCACACATGGGGCATAGCCATGGTCTCTCAGCTCCGCTTAACCACACGGGTCCAGTGTGTGC GGTCCACACATGGGGCATAGCCATGGTCTCTCGGCTCCGCTTAACCACACGGGTCCAGTGTGTGC T C SNORA10,RPS2 Ensembl:ENSG00000206811,Ensembl:ENSG00000140988 snoRNA,Protein coding exon,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:1962437..1962734 26863410 MeRIP-seq:(Medium) rs1555482948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760052,Human_RBP_ID_815726,Human_RBP_ID_894975,Human_RBP_ID_1513613,Human_RBP_ID_2470002,Human_RBP_ID_5097613,Human_RBP_ID_5288528,Human_RBP_ID_8251967,Human_RBP_ID_8429005,Human_RBP_ID_8805337,Human_RBP_ID_17126213,Human_RBP_ID_17669778,Human_RBP_ID_17884576,Human_RBP_ID_18530352,Human_RBP_ID_18674422,Human_RBP_ID_18941059,Human_RBP_ID_21959991,Human_RBP_ID_22705765,Human_RBP_ID_23114163,Human_RBP_ID_23118721,Human_RBP_ID_23127923,Human_RBP_ID_24559032,Human_RBP_ID_26575748,Human_RBP_ID_27796872 RMVar_hsa_circ_84382,RMVar_hsa_circ_116614,RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_95316,RMVar_hsa_circ_175587,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_175585,RMVar_hsa_circ_175586 72872 RMVar_ID_72872 Human_SNP_ID_591122030 m1A Human chr16 + 1962644 1962644 1962644 TGCAGGGATGAGGCGTACCAGCACAGAGCCGCAGCGGCCTGTCACCTGGTGAGGGAAGGAGTCAG TGCAGGGATGAGGCGTACCAGCACAGAGCCGCGGCGGCCTGTCACCTGGTGAGGGAAGGAGTCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1962576..1962775 32194978 MeRIP-seq:(Medium) rs11543075 Functional Loss SNV dbSNP153 33..33 33 - - - 72873 RMVar_ID_72873 Human_SNP_ID_591122320 m1A Human chr16 + 1963104 1963104 1963104 TGAAGCCAAGTGCAACTATGCAGAGCCGAGAGAGTCCCGGCAAGCCCAGCGCAGCCCCCTCCAGG TGAAGCCAAGTGCAACTATGCAGAGCCGAGAGTGTCCCGGCAAGCCCAGCGCAGCCCCCTCCAGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1963101..1963275 26863410 MeRIP-seq:(Medium) rs377714048 Functional Loss SNV dbSNP153 33..33 33 - - - 72874 RMVar_ID_72874 Human_SNP_ID_591122341 m1A Human chr16 + 1963134 1963134 1963134 AGAGTCCCGGCAAGCCCAGCGCAGCCCCCTCCAGGACAGCCGGGTACCTTGAACCTGGTGCGCTG AGAGTCCCGGCAAGCCCAGCGCAGCCCCCTCCGGGACAGCCGGGTACCTTGAACCTGGTGCGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1963126..1963175 32194978 MeRIP-seq:(Medium) rs1227774616 Functional Loss SNV dbSNP153 33..33 33 - - - 72875 RMVar_ID_72875 Human_SNP_ID_591122973 m1A Human chr16 - 1964362 1964362 1964362 CTGGTCACTGGCGCCTTTTCTCCCTTTAGTGGATGCCCGTCACCAAGTTGGGCCGCTTGGTCAAG CTGGTCACTGGCGCCTTTTCTCCCTTTAGTGGTTGCCCGTCACCAAGTTGGGCCGCTTGGTCAAG T A RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr16:1964326..1964400 26863410 MeRIP-seq:(Medium) rs1222079959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233768,Human_RBP_ID_894979,Human_RBP_ID_5355492,Human_RBP_ID_9353087,Human_RBP_ID_17652869,Human_RBP_ID_18189779,Human_RBP_ID_22581708 Human_Splice_Rec_1661078,Human_Splice_Rec_1661079,Human_Splice_Rec_1661088,Human_Splice_Rec_1661089,Human_Splice_Rec_1661099,Human_Splice_Rec_1661105,Human_Splice_Rec_1661116,Human_Splice_Rec_1661117,Human_Splice_Rec_1661124,Human_Splice_Rec_1661125,Human_Splice_Rec_1661130,Human_Splice_Rec_1661131,Human_Splice_Rec_1661136,Human_Splice_Rec_1661137,Human_Splice_Rec_1661144,Human_Splice_Rec_1661154,Human_Splice_Rec_1661155,Human_Splice_Rec_1661169,Human_Splice_Rec_1661176,Human_Splice_Rec_1661177,Human_Splice_Rec_1661183,Human_Splice_Rec_1661187,Human_Splice_Rec_1661190,Human_Splice_Rec_1661191 RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_113861,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_106515,RMVar_hsa_circ_121456,RMVar_hsa_circ_175593,RMVar_hsa_circ_90049,RMVar_hsa_circ_175594,RMVar_hsa_circ_175592,RMVar_hsa_circ_122095,RMVar_hsa_circ_175599,RMVar_hsa_circ_175600 72876 RMVar_ID_72876 Human_SNP_ID_591122974 m1A Human chr16 - 1964362 1964362 1964362 CTGGTCACTGGCGCCTTTTCTCCCTTTAGTGGATGCCCGTCACCAAGTTGGGCCGCTTGGTCAAG CTGGTCACTGGCGCCTTTTCTCCCTTTAGTGGGTGCCCGTCACCAAGTTGGGCCGCTTGGTCAAG T C RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr16:1964326..1964400 26863410 MeRIP-seq:(Medium) rs1222079959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233768,Human_RBP_ID_894979,Human_RBP_ID_5355492,Human_RBP_ID_9353087,Human_RBP_ID_17652869,Human_RBP_ID_18189779,Human_RBP_ID_22581708 Human_Splice_Rec_1661078,Human_Splice_Rec_1661079,Human_Splice_Rec_1661088,Human_Splice_Rec_1661089,Human_Splice_Rec_1661099,Human_Splice_Rec_1661105,Human_Splice_Rec_1661116,Human_Splice_Rec_1661117,Human_Splice_Rec_1661124,Human_Splice_Rec_1661125,Human_Splice_Rec_1661130,Human_Splice_Rec_1661131,Human_Splice_Rec_1661136,Human_Splice_Rec_1661137,Human_Splice_Rec_1661144,Human_Splice_Rec_1661154,Human_Splice_Rec_1661155,Human_Splice_Rec_1661169,Human_Splice_Rec_1661176,Human_Splice_Rec_1661177,Human_Splice_Rec_1661183,Human_Splice_Rec_1661187,Human_Splice_Rec_1661190,Human_Splice_Rec_1661191 RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_113861,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_106515,RMVar_hsa_circ_121456,RMVar_hsa_circ_175593,RMVar_hsa_circ_90049,RMVar_hsa_circ_175594,RMVar_hsa_circ_175592,RMVar_hsa_circ_122095,RMVar_hsa_circ_175599,RMVar_hsa_circ_175600 72877 RMVar_ID_72877 Human_SNP_ID_591123064 m1A Human chr16 + 1964506 1964482 1964506 CGAGCTCCGCGGCCTCGGCCCCGGCCCCGTCCACGGCCGCGACCCCGGCCCCGGATGCCACTGCC CGAGCTCCG________________________CGGCCGCGACCCCGGCCCCGGATGCCACTGCC GCGGCCTCGGCCCCGGCCCCGTCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1964323..1964825 26863196 MeRIP-seq:(Medium) rs762808124 Functional Loss DEL dbSNP153 10..33 33 - - - 72878 RMVar_ID_72878 Human_SNP_ID_591123066 m1A Human chr16 - 1964488 1964488 1964488 CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGGGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA T C RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:1964301..1964756 26863410 MeRIP-seq:(Medium) rs78924165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233769,Human_RBP_ID_9353091,Human_RBP_ID_17883642 Human_Splice_Rec_1661077,Human_Splice_Rec_1661087,Human_Splice_Rec_1661115,Human_Splice_Rec_1661123,Human_Splice_Rec_1661129,Human_Splice_Rec_1661135,Human_Splice_Rec_1661143,Human_Splice_Rec_1661153,Human_Splice_Rec_1661161,Human_Splice_Rec_1661175 RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_106515,RMVar_hsa_circ_121456,RMVar_hsa_circ_175593,RMVar_hsa_circ_90049,RMVar_hsa_circ_175592,RMVar_hsa_circ_175600 72879 RMVar_ID_72879 Human_SNP_ID_591123074 m1A Human chr16 - 1964503 1964497 1964503 AGTGGCATCCGGGGCCGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGG AGTGGCATCCGGGGCCGGGGTCGCGGCCGTGG______CCGGGGCCGAGGCCGCGGAGCTCGCGG GCCCCGT G RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:1964318..1964614 26863410 MeRIP-seq:(Medium) rs1190631392 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_233769,Human_RBP_ID_9353091,Human_RBP_ID_17883642,Human_RBP_ID_18189782 Human_Splice_Rec_1661077,Human_Splice_Rec_1661087,Human_Splice_Rec_1661115,Human_Splice_Rec_1661123,Human_Splice_Rec_1661129,Human_Splice_Rec_1661135,Human_Splice_Rec_1661143,Human_Splice_Rec_1661153,Human_Splice_Rec_1661161,Human_Splice_Rec_1661175 Human_miRNA_ID_1967373 RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_106515,RMVar_hsa_circ_121456,RMVar_hsa_circ_175593,RMVar_hsa_circ_90049,RMVar_hsa_circ_175592,RMVar_hsa_circ_175600 72880 RMVar_ID_72880 Human_SNP_ID_591123076 m1A Human chr16 - 1964503 1964503 1964503 AGTGGCATCCGGGGCCGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGG AGTGGCATCCGGGGCCGGGGTCGCGGCCGTGGCCGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGG T G RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:1964318..1964614 26863410 MeRIP-seq:(Medium) rs575026053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233769,Human_RBP_ID_9353091,Human_RBP_ID_17883642,Human_RBP_ID_18189782 Human_Splice_Rec_1661077,Human_Splice_Rec_1661087,Human_Splice_Rec_1661115,Human_Splice_Rec_1661123,Human_Splice_Rec_1661129,Human_Splice_Rec_1661135,Human_Splice_Rec_1661143,Human_Splice_Rec_1661153,Human_Splice_Rec_1661161,Human_Splice_Rec_1661175 Human_miRNA_ID_1967373 RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_106515,RMVar_hsa_circ_121456,RMVar_hsa_circ_175593,RMVar_hsa_circ_90049,RMVar_hsa_circ_175592,RMVar_hsa_circ_175600 72881 RMVar_ID_72881 Human_SNP_ID_591123251 m1A Human chr16 - 1964785 1964785 1964785 CGACAAAACACGTGAGTCCTGTTGGTCGCTGCAGCGGGCCTCTGCGTGGGCGGCGGGAATCCGCG CGACAAAACACGTGAGTCCTGTTGGTCGCTGCCGCGGGCCTCTGCGTGGGCGGCGGGAATCCGCG T G RPS2 Ensembl:ENSG00000140988 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:1964751..1964825 26863196 MeRIP-seq:(Medium) rs555716540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46219,Human_RBP_ID_277845,Human_RBP_ID_469895,Human_RBP_ID_4354509,Human_RBP_ID_5357340,Human_RBP_ID_6498170,Human_RBP_ID_12683145,Human_RBP_ID_18419438,Human_RBP_ID_19070516,Human_RBP_ID_20169706,Human_RBP_ID_22052749,Human_RBP_ID_22473730,Human_RBP_ID_22800093 Human_Splice_Rec_1661173 RMVar_hsa_circ_106418,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_121456,RMVar_hsa_circ_90049,RMVar_hsa_circ_175592,RMVar_hsa_circ_175600 72882 RMVar_ID_72882 Human_SNP_ID_591123590 m1A Human chr16 + 1965242 1965242 1965242 GGCCGTGGCCGCGGGTGAGATTCGGCGCCCAGAGCCCCCGGGGGCCTCAGCTCACCGCGCGCTGC GGCCGTGGCCGCGGGTGAGATTCGGCGCCCAGGGCCCCCGGGGGCCTCAGCTCACCGCGCGCTGC A G SNHG9,SNORA78 Ensembl:ENSG00000255198,Ensembl:ENSG00000273587 lincRNA,snoRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1965233..1965475 26863196 MeRIP-seq:(Medium) rs771919984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234403,Human_RBP_ID_762447,Human_RBP_ID_816271,Human_RBP_ID_893123,Human_RBP_ID_1526994,Human_RBP_ID_3509901,Human_RBP_ID_5096706,Human_RBP_ID_5288543,Human_RBP_ID_5648223,Human_RBP_ID_8188737,Human_RBP_ID_17669507,Human_RBP_ID_22532649,Human_RBP_ID_22738143,Human_RBP_ID_22800094,Human_RBP_ID_24531161,Human_RBP_ID_27837729 Human_miRNA_ID_3174887,Human_miRNA_ID_3175490,Human_miRNA_ID_3213335 RMVar_hsa_circ_88134,RMVar_hsa_circ_175602 72883 RMVar_ID_72883 Human_SNP_ID_591123709 m1A Human chr16 - 1965454 1965454 1965454 TTTGAAAGACGTGGGACAGCCAAGTTCCCCCAACCCCGCGGTCCTGGCGACGTCGGTGTCAGGCG TTTGAAAGACGTGGGACAGCCAAGTTCCCCCATCCCCGCGGTCCTGGCGACGTCGGTGTCAGGCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:1965279..1965500;chr16:1965325..1965463 26863196 MeRIP-seq:(Medium) rs764517461 Functional Loss SNV dbSNP153 33..33 33 - - - 72884 RMVar_ID_72884 Human_SNP_ID_591123710 m1A Human chr16 - 1965454 1965454 1965454 TTTGAAAGACGTGGGACAGCCAAGTTCCCCCAACCCCGCGGTCCTGGCGACGTCGGTGTCAGGCG TTTGAAAGACGTGGGACAGCCAAGTTCCCCCAGCCCCGCGGTCCTGGCGACGTCGGTGTCAGGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:1965279..1965500;chr16:1965325..1965463 26863196 MeRIP-seq:(Medium) rs764517461 Functional Loss SNV dbSNP153 33..33 33 - - - 72885 RMVar_ID_72885 Human_SNP_ID_591126767 m1A Human chr16 - 1974027 1974027 1974027 ATAGCTGGAAGGAGAGCGGGAGGCGAATGAGCACCACCCACCCCCTCAGTCCCCAGGGCCCCGCC ATAGCTGGAAGGAGAGCGGGAGGCGAATGAGCCCCACCCACCCCCTCAGTCCCCAGGGCCCCGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1974023..1974229 26863196 MeRIP-seq:(Medium) rs772958619 Functional Loss SNV dbSNP153 33..33 33 - - - 72886 RMVar_ID_72886 Human_SNP_ID_591126820 m1A Human chr16 + 1974123 1974123 1974123 AGGGCGGAAAAGCACAGGTACCAGCCTGGGGAAGGGCAGTGGGGCGGGCAGCCAGAGGCCGCGGG AGGGCGGAAAAGCACAGGTACCAGCCTGGGGAGGGGCAGTGGGGCGGGCAGCCAGAGGCCGCGGG A G TBL3 Ensembl:ENSG00000183751 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1974121..1974216 26863196 MeRIP-seq:(Medium) rs1254092805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5357342,Human_RBP_ID_19072901 Human_Splice_Rec_1661210,Human_Splice_Rec_1661252,Human_Splice_Rec_1661262,Human_Splice_Rec_1661302 72887 RMVar_ID_72887 Human_SNP_ID_591126821 m1A Human chr16 + 1974123 1974123 1974123 AGGGCGGAAAAGCACAGGTACCAGCCTGGGGAAGGGCAGTGGGGCGGGCAGCCAGAGGCCGCGGG AGGGCGGAAAAGCACAGGTACCAGCCTGGGGATGGGCAGTGGGGCGGGCAGCCAGAGGCCGCGGG A T TBL3 Ensembl:ENSG00000183751 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1974121..1974216 26863196 MeRIP-seq:(Medium) rs1254092805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5357342,Human_RBP_ID_19072901 Human_Splice_Rec_1661210,Human_Splice_Rec_1661252,Human_Splice_Rec_1661262,Human_Splice_Rec_1661302 72888 RMVar_ID_72888 Human_SNP_ID_591127389 m1A Human chr16 + 1975037 1975037 1975037 CACTGCAGGACCGGTCATGCCTGGCTGTGCTGACTGCCCACTACAGCGCCGTCACCTCACTGGCC CACTGCAGGACCGGTCATGCCTGGCTGTGCTGCCTGCCCACTACAGCGCCGTCACCTCACTGGCC A C TBL3 Ensembl:ENSG00000183751 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1974907..1975055 26863196 MeRIP-seq:(Medium) rs767112487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17872880,Human_RBP_ID_18189789 Human_Splice_Rec_1661221,Human_Splice_Rec_1661271,Human_Splice_Rec_1661313,Human_Splice_Rec_1661347 RMVar_hsa_circ_10728,RMVar_hsa_circ_84606,RMVar_hsa_circ_175603 72889 RMVar_ID_72889 Human_SNP_ID_591127586 m1A Human chr16 - 1975359 1975359 1975359 AGCTGGGACACTGGCTCCTCTGGCAACAGCACAGCAGCCTCCACGCTCTGGAGACGAATTGGGTC AGCTGGGACACTGGCTCCTCTGGCAACAGCACGGCAGCCTCCACGCTCTGGAGACGAATTGGGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1975351..1975425 32194978 MeRIP-seq:(Medium) rs1456128613 Functional Loss SNV dbSNP153 33..33 33 - - - 72890 RMVar_ID_72890 Human_SNP_ID_591131732 m1A Human chr16 + 1984342 1984342 1984342 CGACCGACGCGCGGGGCCGGGGCGCGGGGCGGAGAGACGCGGCCGCCTCGGCCTCGACGCCAGCC CGACCGACGCGCGGGGCCGGGGCGCGGGGCGGGGAGACGCGGCCGCCTCGGCCTCGACGCCAGCC A G GFER Ensembl:ENSG00000127554 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1984082..1984505 26863196 MeRIP-seq:(Medium) rs1308006803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234816,Human_RBP_ID_4394260 72891 RMVar_ID_72891 Human_SNP_ID_591131893 m1A Human chr16 - 1984706 1984706 1984706 GCAGGCCGACCGAGAGTGAGTTCATTCTCCGAACAAAGGCGCCCAAAGCTCCCCACTGTACGGCC GCAGGCCGACCGAGAGTGAGTTCATTCTCCGATCAAAGGCGCCCAAAGCTCCCCACTGTACGGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1984703..1984828 26863196 MeRIP-seq:(Medium) rs1313165659 Functional Loss SNV dbSNP153 33..33 33 - - - 72892 RMVar_ID_72892 Human_SNP_ID_591131924 m1A Human chr16 - 1984771 1984771 1984771 GTGGCGGCCCAGTTCCTCGCGATCCGGCGGGCAGTCCTCCCTAAACTTGGTGTCCCGCTGCGGAA GTGGCGGCCCAGTTCCTCGCGATCCGGCGGGCGGTCCTCCCTAAACTTGGTGTCCCGCTGCGGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1984753..1984854 32194978 MeRIP-seq:(Medium) rs895073717 Functional Loss SNV dbSNP153 33..33 33 - - - 72893 RMVar_ID_72893 Human_SNP_ID_591132662 m1A Human chr16 + 1987107 1987107 1987107 CAGTCACCGAGTGACCACCAAGAGGAAGACCCACCCCACGGCGGGGACAGATGCGGGGTACGTTA CAGTCACCGAGTGACCACCAAGAGGAAGACCCCCCCCACGGCGGGGACAGATGCGGGGTACGTTA A C GFER Ensembl:ENSG00000127554 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12924762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5317282,Human_RBP_ID_21888703,Human_RBP_ID_26329643,Human_RBP_ID_26444704 72894 RMVar_ID_72894 Human_SNP_ID_591132663 m1A Human chr16 + 1987107 1987107 1987107 CAGTCACCGAGTGACCACCAAGAGGAAGACCCACCCCACGGCGGGGACAGATGCGGGGTACGTTA CAGTCACCGAGTGACCACCAAGAGGAAGACCCGCCCCACGGCGGGGACAGATGCGGGGTACGTTA A G GFER Ensembl:ENSG00000127554 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12924762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5317282,Human_RBP_ID_21888703,Human_RBP_ID_26329643,Human_RBP_ID_26444704 72895 RMVar_ID_72895 Human_SNP_ID_591134302 m1A Human chr16 + 1992105 1992105 1992105 GCCTGCCGCTTCGGCGTCGCGCTGGGCCTCGGAGCCTTCCTCGCCTGCGCCGCCTTCCTGCTGCT GCCTGCCGCTTCGGCGTCGCGCTGGGCCTCGGGGCCTTCCTCGCCTGCGCCGCCTTCCTGCTGCT A G SYNGR3 Ensembl:ENSG00000127561 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1992056..1992156 32194978 MeRIP-seq:(Medium) rs1308537701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108154,RMVar_hsa_circ_77828,RMVar_hsa_circ_175606,RMVar_hsa_circ_175607 72896 RMVar_ID_72896 Human_SNP_ID_591136357 m1A Human chr16 + 1997976 1997968 1997976 CTCTGGCTTTGCCAGCAACAACAGGTCCCAGCATCCCAGCCCTTCCCTCCCCTGGCACCTCCCAA CTCTGGCTTTGCCAGCAACAACAGG________TCCCAGCCCTTCCCTCCCCTGGCACCTCCCAA GTCCCAGCA G AC005606.1 Ensembl:ENSG00000260107 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1997927..1998545 32194978 MeRIP-seq:(Medium) rs1341000814 Functional Loss DEL dbSNP153 26..33 33 - - - 72897 RMVar_ID_72897 Human_SNP_ID_591136810 m1A Human chr16 + 1998953 1998953 1998953 TTCCTCCACCCCCGGTGGACACCAGGCAGCTCACCCACACTTACGCTTTTGTGGTGGTGGTGGTG TTCCTCCACCCCCGGTGGACACCAGGCAGCTCGCCCACACTTACGCTTTTGTGGTGGTGGTGGTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1998951..1999025 26863196 MeRIP-seq:(Medium) rs764679677 Functional Loss SNV dbSNP153 33..33 33 - - - 72898 RMVar_ID_72898 Human_SNP_ID_591136819 m1A Human chr16 - 1998968 1998968 1998968 TGTCCCCAGCCCCGCCACCACCACCACCACAAAAGCGTAAGTGTGGGTGAGCTGCCTGGTGTCCA TGTCCCCAGCCCCGCCACCACCACCACCACAAGAGCGTAAGTGTGGGTGAGCTGCCTGGTGTCCA T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1998776..2000275 26863196 MeRIP-seq:(Medium) rs1196271430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22936429 Human_Splice_Rec_1661543,Human_Splice_Rec_1661565,Human_Splice_Rec_1661599,Human_Splice_Rec_1661621,Human_Splice_Rec_1661625 RMVar_hsa_circ_88354,RMVar_hsa_circ_118527,RMVar_hsa_circ_175610,RMVar_hsa_circ_175611,RMVar_hsa_circ_340653 72899 RMVar_ID_72899 Human_SNP_ID_591136905 m1A Human chr16 - 1999092 1999092 1999092 CAGGCTTCAGCGCTGTGGTGCTCCTGAAGGGCACGCCTCCCCCACCCCCGCCGGGCCTGGTGCCC CAGGCTTCAGCGCTGTGGTGCTCCTGAAGGGCCCGCCTCCCCCACCCCCGCCGGGCCTGGTGCCC T G ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1998976..1999150 26863410 MeRIP-seq:(Medium) rs763066670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22497328 Human_Splice_Rec_1661542,Human_Splice_Rec_1661564,Human_Splice_Rec_1661580,Human_Splice_Rec_1661598,Human_Splice_Rec_1661620 RMVar_hsa_circ_88354,RMVar_hsa_circ_118527,RMVar_hsa_circ_175610,RMVar_hsa_circ_175611,RMVar_hsa_circ_340653 72900 RMVar_ID_72900 Human_SNP_ID_591136910 m1A Human chr16 + 1999109 1999109 1999109 GGGGTGGGGGAGGCGTGCCCTTCAGGAGCACCACAGCGCTGAAGCCTGAGGGGTGGCAGGACAAG GGGGTGGGGGAGGCGTGCCCTTCAGGAGCACCGCAGCGCTGAAGCCTGAGGGGTGGCAGGACAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:1998951..1999125 26863196 MeRIP-seq:(Medium) rs751486456 Functional Loss SNV dbSNP153 33..33 33 - - - 72901 RMVar_ID_72901 Human_SNP_ID_591137142 m1A Human chr16 + 1999596 1999596 1999596 CAGGGGAAGGACCCCAGGGGCCTTGGGAGCCCAGGGGGTTCCTTGGGGGCACTCCGAGCAGGGGC CAGGGGAAGGACCCCAGGGGCCTTGGGAGCCCGGGGGGTTCCTTGGGGGCACTCCGAGCAGGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1999547..1999714 26863196 MeRIP-seq:(Medium) rs1287684376 Functional Loss SNV dbSNP153 33..33 33 - - - 72902 RMVar_ID_72902 Human_SNP_ID_591137176 m1A Human chr16 + 1999639 1999639 1999639 TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCATGTGTCCATTAACGACGACGGCAACTGGCCCC TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCCTGTGTCCATTAACGACGACGGCAACTGGCCCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1999501..1999730 26863196 MeRIP-seq:(Medium) rs2286469 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8864,GWAS_ID_8865,GWAS_ID_8866,GWAS_ID_8867,GWAS_ID_8868,GWAS_ID_8869,GWAS_ID_8870,GWAS_ID_8871,GWAS_ID_8872,GWAS_ID_8873 72903 RMVar_ID_72903 Human_SNP_ID_591137177 m1A Human chr16 + 1999639 1999639 1999639 TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCATGTGTCCATTAACGACGACGGCAACTGGCCCC TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCGTGTGTCCATTAACGACGACGGCAACTGGCCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1999501..1999730 26863196 MeRIP-seq:(Medium) rs2286469 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - GWAS_ID_8864,GWAS_ID_8865,GWAS_ID_8866,GWAS_ID_8867,GWAS_ID_8868,GWAS_ID_8869,GWAS_ID_8870,GWAS_ID_8871,GWAS_ID_8872,GWAS_ID_8873 72904 RMVar_ID_72904 Human_SNP_ID_591137178 m1A Human chr16 + 1999639 1999639 1999639 TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCATGTGTCCATTAACGACGACGGCAACTGGCCCC TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCTTGTGTCCATTAACGACGACGGCAACTGGCCCC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1999501..1999730 26863196 MeRIP-seq:(Medium) rs2286469 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8864,GWAS_ID_8865,GWAS_ID_8866,GWAS_ID_8867,GWAS_ID_8868,GWAS_ID_8869,GWAS_ID_8870,GWAS_ID_8871,GWAS_ID_8872,GWAS_ID_8873 72905 RMVar_ID_72905 Human_SNP_ID_591137328 m1A Human chr16 - 1999848 1999848 1999848 GGCGGCCCGGCCCTGCAGGAGCTTCTGAGCACACGCCCCACGGGCTCCGTCTCCTCCACACTGGG GGCGGCCCGGCCCTGCAGGAGCTTCTGAGCACGCGCCCCACGGGCTCCGTCTCCTCCACACTGGG T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12149722 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6498226,Human_RBP_ID_27238139 RMVar_hsa_circ_118527,RMVar_hsa_circ_82495,RMVar_hsa_circ_175611,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72906 RMVar_ID_72906 Human_SNP_ID_591137504 m1A Human chr16 + 2000127 2000127 2000127 TCCTCCTCCTGGAAGGCACTCCTGCCTCTGGCAGGGATGGCGTACGGCAGCGCCAACCCCACAGG TCCTCCTCCTGGAAGGCACTCCTGCCTCTGGCGGGGATGGCGTACGGCAGCGCCAACCCCACAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2000101..2000175 26863196 MeRIP-seq:(Medium) rs1308900383 Functional Loss SNV dbSNP153 33..33 33 - - - 72907 RMVar_ID_72907 Human_SNP_ID_591138026 m1A Human chr16 - 2001018 2001016 2001018 TCCCCGTGGCCCCCGGCGCTCACCCCGGACTCAGGGCGAAGGCCCAGGTGAGTAAGCCCTACCTG TCCCCGTGGCCCCCGGCGCTCACCCCGGACTC__GGCGAAGGCCCAGGTGAGTAAGCCCTACCTG CCT C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2001001..2001025 26863196 MeRIP-seq:(Medium) rs1429053951 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3948493,Human_RBP_ID_18437230,Human_RBP_ID_18985116,Human_RBP_ID_26329645 Human_Splice_Rec_1661537,Human_Splice_Rec_1661559,Human_Splice_Rec_1661577,Human_Splice_Rec_1661593,Human_Splice_Rec_1661615,Human_Splice_Rec_1661643,Human_Splice_Rec_1661649,Human_Splice_Rec_1661657 Human_miRNA_ID_1973515,Human_miRNA_ID_1975694,Human_miRNA_ID_2613494 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72908 RMVar_ID_72908 Human_SNP_ID_591138027 m1A Human chr16 - 2001018 2001018 2001018 TCCCCGTGGCCCCCGGCGCTCACCCCGGACTCAGGGCGAAGGCCCAGGTGAGTAAGCCCTACCTG TCCCCGTGGCCCCCGGCGCTCACCCCGGACTCGGGGCGAAGGCCCAGGTGAGTAAGCCCTACCTG T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2001001..2001025 26863196 MeRIP-seq:(Medium) rs1415849114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3948493,Human_RBP_ID_18437230,Human_RBP_ID_18985116,Human_RBP_ID_26329645 Human_Splice_Rec_1661537,Human_Splice_Rec_1661559,Human_Splice_Rec_1661577,Human_Splice_Rec_1661593,Human_Splice_Rec_1661615,Human_Splice_Rec_1661643,Human_Splice_Rec_1661649,Human_Splice_Rec_1661657 Human_miRNA_ID_1973515,Human_miRNA_ID_1975694,Human_miRNA_ID_2613494 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72909 RMVar_ID_72909 Human_SNP_ID_591138084 m1A Human chr16 - 2001084 2001084 2001084 GAGTGAGGATCAGGAGGAAGGCGGTAGGCCCAAGAAGGAGGAGGCAGCGGCGCGGGGACCTGAGG GAGTGAGGATCAGGAGGAAGGCGGTAGGCCCAGGAAGGAGGAGGCAGCGGCGCGGGGACCTGAGG T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2001001..2001228 26863196 MeRIP-seq:(Medium) rs1193712945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4354800,Human_RBP_ID_17872927,Human_RBP_ID_18985117,Human_RBP_ID_22944958,Human_RBP_ID_26328461 Human_Splice_Rec_1661537,Human_Splice_Rec_1661559,Human_Splice_Rec_1661577,Human_Splice_Rec_1661593,Human_Splice_Rec_1661615,Human_Splice_Rec_1661643,Human_Splice_Rec_1661649,Human_Splice_Rec_1661657 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72910 RMVar_ID_72910 Human_SNP_ID_591138329 m1A Human chr16 - 2001616 2001616 2001616 CCGAGTGGCCCGGGCTGGCACTCGCGGAGCCCAGCAGAGCCGCCGAGGAAGCTGGAGGTACAAAA CCGAGTGGCCCGGGCTGGCACTCGCGGAGCCCTGCAGAGCCGCCGAGGAAGCTGGAGGTACAAAA T A ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2000401..2002681 26863196 MeRIP-seq:(Medium) rs752952198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3948495,Human_RBP_ID_9286051,Human_RBP_ID_18985119 Human_Splice_Rec_1661534,Human_Splice_Rec_1661535,Human_Splice_Rec_1661556,Human_Splice_Rec_1661557,Human_Splice_Rec_1661574,Human_Splice_Rec_1661575,Human_Splice_Rec_1661590,Human_Splice_Rec_1661591,Human_Splice_Rec_1661612,Human_Splice_Rec_1661613,Human_Splice_Rec_1661640,Human_Splice_Rec_1661641,Human_Splice_Rec_1661647,Human_Splice_Rec_1661654,Human_Splice_Rec_1661655 Human_miRNA_ID_2017928,Human_miRNA_ID_2395818,Human_miRNA_ID_2554564,Human_miRNA_ID_3069612 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72911 RMVar_ID_72911 Human_SNP_ID_591138330 m1A Human chr16 - 2001616 2001616 2001616 CCGAGTGGCCCGGGCTGGCACTCGCGGAGCCCAGCAGAGCCGCCGAGGAAGCTGGAGGTACAAAA CCGAGTGGCCCGGGCTGGCACTCGCGGAGCCCGGCAGAGCCGCCGAGGAAGCTGGAGGTACAAAA T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2000401..2002681 26863196 MeRIP-seq:(Medium) rs752952198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3948495,Human_RBP_ID_9286051,Human_RBP_ID_18985119 Human_Splice_Rec_1661534,Human_Splice_Rec_1661535,Human_Splice_Rec_1661556,Human_Splice_Rec_1661557,Human_Splice_Rec_1661574,Human_Splice_Rec_1661575,Human_Splice_Rec_1661590,Human_Splice_Rec_1661591,Human_Splice_Rec_1661612,Human_Splice_Rec_1661613,Human_Splice_Rec_1661640,Human_Splice_Rec_1661641,Human_Splice_Rec_1661647,Human_Splice_Rec_1661654,Human_Splice_Rec_1661655 Human_miRNA_ID_2017928,Human_miRNA_ID_2395818,Human_miRNA_ID_2554564,Human_miRNA_ID_3069612 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 72912 RMVar_ID_72912 Human_SNP_ID_591138856 m1A Human chr16 - 2002714 2002714 2002714 CCTGTGCCTTGTAGATCTTCACATATGAGCGCAAGTGGTACTCGCGCAAGGACCTGGCCCGGCAT CCTGTGCCTTGTAGATCTTCACATATGAGCGCCAGTGGTACTCGCGCAAGGACCTGGCCCGGCAT T G ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2002543..2002841 32194978 MeRIP-seq:(Medium) rs750192848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889304,Human_RBP_ID_1003304,Human_RBP_ID_1513699,Human_RBP_ID_3492319,Human_RBP_ID_3948496,Human_RBP_ID_9284409,Human_RBP_ID_9372072,Human_RBP_ID_12683261,Human_RBP_ID_23681886 Human_Splice_Rec_1661532,Human_Splice_Rec_1661552,Human_Splice_Rec_1661586,Human_Splice_Rec_1661608,Human_Splice_Rec_1661638 Human_miRNA_ID_2150106,Human_miRNA_ID_2943720 RMVar_hsa_circ_82495,RMVar_hsa_circ_340653,RMVar_hsa_circ_99405,RMVar_hsa_circ_175612,RMVar_hsa_circ_175614,RMVar_hsa_circ_76970,RMVar_hsa_circ_107258,RMVar_hsa_circ_175613,RMVar_hsa_circ_175615 72913 RMVar_ID_72913 Human_SNP_ID_591139006 m1A Human chr16 + 2003064 2003063 2003065 GCTGCCTCCGCATGTGCTGCTCCAGGTCCCCGAAGAGGCTGAAAGGTGGCAGCTCGGGGCACCGC GCTGCCTCCGCATGTGCTGCTCCAGGTCCCCG__GAGGCTGAAAGGTGGCAGCTCGGGGCACCGC GAA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2002988..2003137 32194978 MeRIP-seq:(Medium) rs776406705 Functional Loss DEL dbSNP153 33..34 33 - - - 72914 RMVar_ID_72914 Human_SNP_ID_591139425 m1A Human chr16 + 2004099 2004099 2004099 CTGTCGCTCTGCGGAGCTTTCCAGGACAGAGAAGAAACGTGTTCCAAGCAGCTGCTAAGGGAATA CTGTCGCTCTGCGGAGCTTTCCAGGACAGAGACGAAACGTGTTCCAAGCAGCTGCTAAGGGAATA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2004097..2004516 26863196 MeRIP-seq:(Medium) rs1480867005 Functional Loss SNV dbSNP153 33..33 33 - - - 72915 RMVar_ID_72915 Human_SNP_ID_591140497 m1A Human chr16 + 2007165 2007165 2007165 AAGGAGCCCAGATGGGGACAGCAGCAGCAGGGAGCATCTTACAGAGGGCCAGGGCCATGGGGGAC AAGGAGCCCAGATGGGGACAGCAGCAGCAGGGGGCATCTTACAGAGGGCCAGGGCCATGGGGGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2007163..2007309 26863196 MeRIP-seq:(Medium) rs890242110 Functional Loss SNV dbSNP153 33..33 33 - - - 72916 RMVar_ID_72916 Human_SNP_ID_591141086 m1A Human chr16 + 2008817 2008817 2008817 CTGGCAGTGCAGTGAGGGTGGAGGAACGCTGCATGGTACCCTCTGACCCCTCCACGGCTTCCAAG CTGGCAGTGCAGTGAGGGTGGAGGAACGCTGCGTGGTACCCTCTGACCCCTCCACGGCTTCCAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2008814..2008971 26863196 MeRIP-seq:(Medium) rs1567345469 Functional Loss SNV dbSNP153 33..33 33 - - - 72917 RMVar_ID_72917 Human_SNP_ID_591141391 m1A Human chr16 + 2009625 2009624 2009625 GCGGTAGCACACCGGGTGGTCGCAGCGGCCCCAGCGCCGTGGCCTCCAGGTCTCCGCAGCACAGC GCGGTAGCACACCGGGTGGTCGCAGCGGCCCC_GCGCCGTGGCCTCCAGGTCTCCGCAGCACAGC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:2009479..2009775;chr16:2009310..2009775;chr16:2009535..2009712 26863196 MeRIP-seq:(Medium) rs1567345850 Functional Loss DEL dbSNP153 33..33 33 - - - 72918 RMVar_ID_72918 Human_SNP_ID_591141394 m1A Human chr16 + 2009625 2009625 2009625 GCGGTAGCACACCGGGTGGTCGCAGCGGCCCCAGCGCCGTGGCCTCCAGGTCTCCGCAGCACAGC GCGGTAGCACACCGGGTGGTCGCAGCGGCCCCGGCGCCGTGGCCTCCAGGTCTCCGCAGCACAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:2009479..2009775;chr16:2009310..2009775;chr16:2009535..2009712 26863196 MeRIP-seq:(Medium) rs1356079323 Functional Loss SNV dbSNP153 33..33 33 - - - 72919 RMVar_ID_72919 Human_SNP_ID_591141423 m1A Human chr16 - 2009672 2009672 2009672 GAGGCGGAGGCGGCGGCAGCTCCTGAGCGGGGAGGCGGGAGCTGCGTGCTGTGCTGCGGAGACCT GAGGCGGAGGCGGCGGCAGCTCCTGAGCGGGGGGGCGGGAGCTGCGTGCTGTGCTGCGGAGACCT T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2009583..2009755 26863196 MeRIP-seq:(Medium) rs1286258072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_127129,Human_RBP_ID_234028,Human_RBP_ID_8086735,Human_RBP_ID_9324834,Human_RBP_ID_22532651,Human_RBP_ID_22944803,Human_RBP_ID_26780037 RMVar_hsa_circ_99405,RMVar_hsa_circ_107258,RMVar_hsa_circ_175613,RMVar_hsa_circ_175615 72920 RMVar_ID_72920 Human_SNP_ID_591141433 m1A Human chr16 + 2009681 2009681 2009681 CAGCACAGCACGCAGCTCCCGCCTCCCCGCTCAGGAGCTGCCGCCGCCTCCGCCTCCATGTCCGC CAGCACAGCACGCAGCTCCCGCCTCCCCGCTCGGGAGCTGCCGCCGCCTCCGCCTCCATGTCCGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2009593..2009723 26863410 MeRIP-seq:(Medium) rs1255597953 Functional Loss SNV dbSNP153 33..33 33 - - - 72921 RMVar_ID_72921 Human_SNP_ID_591147460 m1A Human chr16 - 2026991 2026991 2026991 CGGCTCCGGCGCGGCCATGGCGCCCGCTGCCCACCGGCCGCCCGCGGGCAGGGGCGCGGGGGAGC CGGCTCCGGCGCGGCCATGGCGCCCGCTGCCCCCCGGCCGCCCGCGGGCAGGGGCGCGGGGGAGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2026901..2027148 26863410 MeRIP-seq:(Medium) rs1056231123 Functional Loss SNV dbSNP153 33..33 33 - - - 72922 RMVar_ID_72922 Human_SNP_ID_591147484 m1A Human chr16 + 2027067 2027067 2027067 CCTGTGCCGCTTGGTGCGCGGAGAGCAGGGCTACGGCTTCCACCTGCACGGCGAGAAGGGCCGCC CCTGTGCCGCTTGGTGCGCGGAGAGCAGGGCTGCGGCTTCCACCTGCACGGCGAGAAGGGCCGCC A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2026901..2027125 26863196 MeRIP-seq:(Medium) rs949666306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4354958,Human_RBP_ID_23681934 72923 RMVar_ID_72923 Human_SNP_ID_591148356 m1A Human chr16 + 2029637 2029637 2029637 GGAGGGGCAGACTCGGCTGCTGGTGGTGGACCAGGAGACAGATGAGGAGCTCCGCCGGCGGCAGC GGAGGGGCAGACTCGGCTGCTGGTGGTGGACCGGGAGACAGATGAGGAGCTCCGCCGGCGGCAGC A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2029576..2029750 26863196 MeRIP-seq:(Medium) rs1460667729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392766,Human_RBP_ID_5237204,Human_RBP_ID_17872990 Human_Splice_Rec_1661668,Human_Splice_Rec_1661672,Human_Splice_Rec_1661684 RMVar_hsa_circ_378712 72924 RMVar_ID_72924 Human_SNP_ID_591148357 m1A Human chr16 + 2029637 2029637 2029637 GGAGGGGCAGACTCGGCTGCTGGTGGTGGACCAGGAGACAGATGAGGAGCTCCGCCGGCGGCAGC GGAGGGGCAGACTCGGCTGCTGGTGGTGGACCTGGAGACAGATGAGGAGCTCCGCCGGCGGCAGC A T SLC9A3R2 Ensembl:ENSG00000065054 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2029576..2029750 26863196 MeRIP-seq:(Medium) rs1460667729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392766,Human_RBP_ID_5237204,Human_RBP_ID_17872990 Human_Splice_Rec_1661668,Human_Splice_Rec_1661672,Human_Splice_Rec_1661684 RMVar_hsa_circ_378712 72925 RMVar_ID_72925 Human_SNP_ID_591150105 m1A Human chr16 + 2035044 2035035 2035044 GCCCAGCTGAGCCCCTGTGGGGCCAGGGAGCCACAGGCTTGTCCCTGGAGTTTCTGGTGTGACGG GCCCAGCTGAGCCCCTGTGGGGCC_________CAGGCTTGTCCCTGGAGTTTCTGGTGTGACGG CAGGGAGCCA C SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2035042..2035253 26863196 MeRIP-seq:(Medium) rs1221233263 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_378712 72926 RMVar_ID_72926 Human_SNP_ID_591150739 m1A Human chr16 + 2036415 2036415 2036415 TCAGGGCTATGGGTTCAACCTGCATAGTGACAAGTCCCGGCCCGGCCAGTACATCCGCTCTGTGG TCAGGGCTATGGGTTCAACCTGCATAGTGACACGTCCCGGCCCGGCCAGTACATCCGCTCTGTGG A C SLC9A3R2 Ensembl:ENSG00000065054 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2036280..2036414 26863196 MeRIP-seq:(Medium) rs781345872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1661670,Human_Splice_Rec_1661674,Human_Splice_Rec_1661675,Human_Splice_Rec_1661686,Human_Splice_Rec_1661687,Human_Splice_Rec_1661696,Human_Splice_Rec_1661697,Human_Splice_Rec_1661706,Human_Splice_Rec_1661707,Human_Splice_Rec_1661718,Human_Splice_Rec_1661719,Human_Splice_Rec_1661722,Human_Splice_Rec_1661723,Human_Splice_Rec_1661732,Human_Splice_Rec_1661733,Human_Splice_Rec_1661741 RMVar_hsa_circ_378712 72927 RMVar_ID_72927 Human_SNP_ID_591150740 m1A Human chr16 - 2036417 2036417 2036417 GTCCACAGAGCGGATGTACTGGCCGGGCCGGGACTTGTCACTATGCAGGTTGAACCCATAGCCCT GTCCACAGAGCGGATGTACTGGCCGGGCCGGGGCTTGTCACTATGCAGGTTGAACCCATAGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2036276..2036516 26863196 MeRIP-seq:(Medium) rs776205113 Functional Loss SNV dbSNP153 33..33 33 - - - 72928 RMVar_ID_72928 Human_SNP_ID_591150972 m1A Human chr16 + 2036783 2036783 2036783 ACTGCGCCATGCTGAGGTGGTGGCCAGCATCAAGGCACGGGAGGACGAGGCCCGGCTGCTGGTCG ACTGCGCCATGCTGAGGTGGTGGCCAGCATCAGGGCACGGGAGGACGAGGCCCGGCTGCTGGTCG A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2036691..2036821 26863196 MeRIP-seq:(Medium) rs753593818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18985122 Human_Splice_Rec_1661676,Human_Splice_Rec_1661677,Human_Splice_Rec_1661688,Human_Splice_Rec_1661689,Human_Splice_Rec_1661698,Human_Splice_Rec_1661699,Human_Splice_Rec_1661708,Human_Splice_Rec_1661709,Human_Splice_Rec_1661720,Human_Splice_Rec_1661724,Human_Splice_Rec_1661725,Human_Splice_Rec_1661734,Human_Splice_Rec_1661735,Human_Splice_Rec_1661742,Human_Splice_Rec_1661743 RMVar_hsa_circ_378712 72929 RMVar_ID_72929 Human_SNP_ID_591151398 m1A Human chr16 + 2037595 2037595 2037595 CCCGAAGTGACCTGCCTGGTTCCGACAAGGACACTGAGGTATGGATGTTCTCCACTCCTGAGCTC CCCGAAGTGACCTGCCTGGTTCCGACAAGGACCCTGAGGTATGGATGTTCTCCACTCCTGAGCTC A C SLC9A3R2 Ensembl:ENSG00000065054 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2036723..2037776 26863196 MeRIP-seq:(Medium) rs751900657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26809845 Human_Splice_Rec_1661680,Human_Splice_Rec_1661681,Human_Splice_Rec_1661692,Human_Splice_Rec_1661693,Human_Splice_Rec_1661702,Human_Splice_Rec_1661703,Human_Splice_Rec_1661712,Human_Splice_Rec_1661713,Human_Splice_Rec_1661728,Human_Splice_Rec_1661729,Human_Splice_Rec_1661738,Human_Splice_Rec_1661739,Human_Splice_Rec_1661746,Human_Splice_Rec_1661747 RMVar_hsa_circ_378712 72930 RMVar_ID_72930 Human_SNP_ID_591151619 m1A Human chr16 + 2038122 2038122 2038122 CCATTGCCCAGAAATCAGCCCCAGCCCCGGTGAGCCCCCATCCTGCCCCTGCCCACCAGGTACTG CCATTGCCCAGAAATCAGCCCCAGCCCCGGTGGGCCCCCATCCTGCCCCTGCCCACCAGGTACTG A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2038076..2038300 26863196 MeRIP-seq:(Medium) rs559949275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470077,Human_RBP_ID_889308,Human_RBP_ID_23682016 Human_miRNA_ID_676958 Clinvar_Rec_309,Clinvar_Rec_310 72931 RMVar_ID_72931 Human_SNP_ID_591151650 m1A Human chr16 + 2038220 2038217 2038221 CCCAGAGATGTGAGAGAGAGTCAGAGACAGAGACAGAGAGAGAGAGAGAGAGACACAGAGAGAGA CCCAGAGATGTGAGAGAGAGTCAGAGACAG____AGAGAGAGAGAGAGAGAGACACAGAGAGAGA GAGAC G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2037808..2038526 26863196 MeRIP-seq:(Medium) rs1028937183 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_128123,Human_RBP_ID_763349,Human_RBP_ID_2470071,Human_RBP_ID_5114089,Human_RBP_ID_5141794,Human_RBP_ID_17883645,Human_RBP_ID_18163468,Human_RBP_ID_23682017 72932 RMVar_ID_72932 Human_SNP_ID_591151944 m1A Human chr16 + 2038752 2038752 2038752 GGCTCTCCGAGGGGCCTGAGGATGGAGGCCCCACGTCCCCGAGGAGGGCGGCCTCTGGACAGGCC GGCTCTCCGAGGGGCCTGAGGATGGAGGCCCCGCGTCCCCGAGGAGGGCGGCCTCTGGACAGGCC A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2038701..2038900 26863196 MeRIP-seq:(Medium) rs1016367130 Functional Loss SNV dbSNP153 33..33 33 - - - 72933 RMVar_ID_72933 Human_SNP_ID_591151961 m1A Human chr16 - 2038775 2038775 2038775 GGGAGCTGCCGCGCGGAATGAGGGGCCTGTCCAGAGGCCGCCCTCCTCGGGGACGTGGGGCCTCC GGGAGCTGCCGCGCGGAATGAGGGGCCTGTCCGGAGGCCGCCCTCCTCGGGGACGTGGGGCCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2038725..2038922 26863196 MeRIP-seq:(Medium) rs1183405462 Functional Loss SNV dbSNP153 33..33 33 - - - 72934 RMVar_ID_72934 Human_SNP_ID_591152506 m1A Human chr16 - 2040188 2040188 2040188 ACAGAATCGCCAACAGGCTGAGGTGGACCAAGAAGGCAACCAAGTCCCCAGAGGAGACCCGCGCC ACAGAATCGCCAACAGGCTGAGGTGGACCAAGGAGGCAACCAAGTCCCCAGAGGAGACCCGCGCC T C NTHL1 Ensembl:ENSG00000065057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2039882..2040200 26863196 MeRIP-seq:(Medium) rs879181418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1003373 Human_Splice_Rec_1661756,Human_Splice_Rec_1661757,Human_Splice_Rec_1661764,Human_Splice_Rec_1661765,Human_Splice_Rec_1661767,Human_Splice_Rec_1661772,Human_Splice_Rec_1661773,Human_Splice_Rec_1661780,Human_Splice_Rec_1661781,Human_Splice_Rec_1661790,Human_Splice_Rec_1661791,Human_Splice_Rec_1661796,Human_Splice_Rec_1661797,Human_Splice_Rec_1661804,Human_Splice_Rec_1661805,Human_Splice_Rec_1661814,Human_Splice_Rec_1661815,Human_Splice_Rec_1661818,Human_Splice_Rec_1661819,Human_Splice_Rec_1661830,Human_Splice_Rec_1661831 Human_miRNA_ID_2434660 RMVar_hsa_circ_175616,RMVar_hsa_circ_96467 72935 RMVar_ID_72935 Human_SNP_ID_591153556 m1A Human chr16 - 2043618 2043618 2043618 CCGAGCTGGTGGCGCTGCCGGGTGTTGGGCCCAAGATGGCACACCTGGCTATGGCTGTGGCCTGG CCGAGCTGGTGGCGCTGCCGGGTGTTGGGCCCCAGATGGCACACCTGGCTATGGCTGTGGCCTGG T G NTHL1 Ensembl:ENSG00000065057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2043526..2043664 26863196 MeRIP-seq:(Medium) rs1247089981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23682091 Human_Splice_Rec_1661755,Human_Splice_Rec_1661763,Human_Splice_Rec_1661771,Human_Splice_Rec_1661779,Human_Splice_Rec_1661789,Human_Splice_Rec_1661795,Human_Splice_Rec_1661803,Human_Splice_Rec_1661813,Human_Splice_Rec_1661817,Human_Splice_Rec_1661827 RMVar_hsa_circ_38350,RMVar_hsa_circ_175616,RMVar_hsa_circ_96467,RMVar_hsa_circ_366793 72936 RMVar_ID_72936 Human_SNP_ID_591153964 m1A Human chr16 + 2044727 2044727 2044727 CCACCGTCAGGCCCCGCGCCCGCAGTCGCTGCATGGCGCCCGCCGTCACCTGGTCTTTGGTTTGG CCACCGTCAGGCCCCGCGCCCGCAGTCGCTGCCTGGCGCCCGCCGTCACCTGGTCTTTGGTTTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2044676..2044775 26863196 MeRIP-seq:(Medium) rs759156239 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8874,GWAS_ID_8875,GWAS_ID_8876 72937 RMVar_ID_72937 Human_SNP_ID_591153965 m1A Human chr16 + 2044727 2044727 2044727 CCACCGTCAGGCCCCGCGCCCGCAGTCGCTGCATGGCGCCCGCCGTCACCTGGTCTTTGGTTTGG CCACCGTCAGGCCCCGCGCCCGCAGTCGCTGCGTGGCGCCCGCCGTCACCTGGTCTTTGGTTTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2044676..2044775 26863196 MeRIP-seq:(Medium) rs759156239 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8874,GWAS_ID_8875,GWAS_ID_8876 72938 RMVar_ID_72938 Human_SNP_ID_591154559 m1A Human chr16 - 2046368 2046368 2046368 CCCCACCAGAGGGACTGCGTGGTGCTTTTTGCAGAAGCGAGGAAAAGCCACAGCCCCGTGAAGCG CCCCACCAGAGGGACTGCGTGGTGCTTTTTGCGGAAGCGAGGAAAAGCCACAGCCCCGTGAAGCG T C NTHL1 Ensembl:ENSG00000065057 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2046304..2046974 26863410 MeRIP-seq:(Medium) rs1411270811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45992,Human_RBP_ID_470110,Human_RBP_ID_4355190 Human_Splice_Rec_1661809 72939 RMVar_ID_72939 Human_SNP_ID_591154951 m1A Human chr16 - 2047676 2047676 2047676 GTAGCGCCGCGCCGTGGCTGGAGCGTGGGAGGAGGCGGGATAGGGGCTGCAGGCTGGAGTCCCGG GTAGCGCCGCGCCGTGGCTGGAGCGTGGGAGGTGGCGGGATAGGGGCTGCAGGCTGGAGTCCCGG T A NTHL1 Ensembl:ENSG00000065057 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2047669..2047820 26863196 MeRIP-seq:(Medium) rs1162972566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5359250 72940 RMVar_ID_72940 Human_SNP_ID_591155028 m1A Human chr16 + 2047780 2047780 2047780 CCCTACACCCCCGCGGCCCAGCCCCGGGTCCCAGGCTCCGGCTCCGGGTCAGCATCCTCGCGCTC CCCTACACCCCCGCGGCCCAGCCCCGGGTCCCGGGCTCCGGCTCCGGGTCAGCATCCTCGCGCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2047613..2047850 26863196 MeRIP-seq:(Medium) rs781328762 Functional Loss SNV dbSNP153 33..33 33 - - - 72941 RMVar_ID_72941 Human_SNP_ID_591155254 m1A Human chr16 - 2048067 2048067 2048067 GACCGCCACTTGCCCCGTGGGGACCGCCACTTACCCCGCGCCGCGCCACCGCGCTCCGGGCCGCC GACCGCCACTTGCCCCGTGGGGACCGCCACTTGCCCCGCGCCGCGCCACCGCGCTCCGGGCCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2048020..2048091 26863196 MeRIP-seq:(Medium) rs796053514 Functional Loss SNV dbSNP153 33..33 33 - - - 72942 RMVar_ID_72942 Human_SNP_ID_591155498 m1A Human chr16 + 2048656 2048656 2048656 ACCAACAAGCAAAGATTCAGGCTTGAAGGAGAAGTTTAAGATTCTGTTGGGACTGGGAACACCGA ACCAACAAGCAAAGATTCAGGCTTGAAGGAGAGGTTTAAGATTCTGTTGGGACTGGGAACACCGA A G TSC2 Ensembl:ENSG00000103197 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2048605..2048693 26863196 MeRIP-seq:(Medium) rs1263108967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12684227 Human_Splice_Rec_1661838,Human_Splice_Rec_1661839,Human_Splice_Rec_1661866,Human_Splice_Rec_1661867,Human_Splice_Rec_1661944,Human_Splice_Rec_1661945,Human_Splice_Rec_1662024,Human_Splice_Rec_1662025,Human_Splice_Rec_1662126,Human_Splice_Rec_1662127,Human_Splice_Rec_1662162,Human_Splice_Rec_1662163,Human_Splice_Rec_1662168,Human_Splice_Rec_1662169,Human_Splice_Rec_1662192,Human_Splice_Rec_1662193,Human_Splice_Rec_1662222,Human_Splice_Rec_1662223,Human_Splice_Rec_1662304,Human_Splice_Rec_1662305,Human_Splice_Rec_1662384,Human_Splice_Rec_1662385,Human_Splice_Rec_1662462,Human_Splice_Rec_1662463,Human_Splice_Rec_1662540,Human_Splice_Rec_1662541,Human_Splice_Rec_1662568,Human_Splice_Rec_1662569,Human_Splice_Rec_1662650,Human_Splice_Rec_1662651,Human_Splice_Rec_1662696,Human_Splice_Rec_1662697,Human_Splice_Rec_1662772,Human_Splice_Rec_1662773,Human_Splice_Rec_1662852,Human_Splice_Rec_1662853,Human_Splice_Rec_1662858,Human_Splice_Rec_1662859,Human_Splice_Rec_1662934,Human_Splice_Rec_1662935,Human_Splice_Rec_1663008,Human_Splice_Rec_1663009,Human_Splice_Rec_1663036,Human_Splice_Rec_1663037,Human_Splice_Rec_1663116,Human_Splice_Rec_1663117,Human_Splice_Rec_1663194,Human_Splice_Rec_1663195,Human_Splice_Rec_1663274,Human_Splice_Rec_1663275,Human_Splice_Rec_1663351,Human_Splice_Rec_1663429,Human_Splice_Rec_1663435 RMVar_hsa_circ_175617,RMVar_hsa_circ_79940,RMVar_hsa_circ_354229 72943 RMVar_ID_72943 Human_SNP_ID_591170123 m1A Human chr16 - 2081376 2081374 2081376 GCCTCGAGGCCAGGCTCCGCCAGGCACCTCAGAGCAGCGGCCTCCAGCCCACAGCCTCACAGTCC GCCTCGAGGCCAGGCTCCGCCAGGCACCTCAG__CAGCGGCCTCCAGCCCACAGCCTCACAGTCC GCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2081368..2081517 26863196 MeRIP-seq:(Medium) rs1439821345 Functional Loss DEL dbSNP153 33..34 33 - - - 72944 RMVar_ID_72944 Human_SNP_ID_591170136 m1A Human chr16 + 2081409 2081408 2081410 CTGAGGTGCCTGGCGGAGCCTGGCCTCGAGGCAGGGGCTGAGCGGGGCAGCAGGGTGGGTGGCCG CTGAGGTGCCTGGCGGAGCCTGGCCTCGAGGC__GGGCTGAGCGGGGCAGCAGGGTGGGTGGCCG CAG C TSC2 Ensembl:ENSG00000103197 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2081360..2081452 26863196 MeRIP-seq:(Medium) rs1162384723 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_82864,RMVar_hsa_circ_81580,RMVar_hsa_circ_175626,RMVar_hsa_circ_175630,RMVar_hsa_circ_110039,RMVar_hsa_circ_175634,RMVar_hsa_circ_105492,RMVar_hsa_circ_121572,RMVar_hsa_circ_175640,RMVar_hsa_circ_103353,RMVar_hsa_circ_175641,RMVar_hsa_circ_175639,RMVar_hsa_circ_2424 72945 RMVar_ID_72945 Human_SNP_ID_591170361 m1A Human chr16 + 2081770 2081770 2081770 TCACTGTCGGTGCCGGCAGCCAGCACGGCCAAACCCCCTCCTCTGCCTCGCTCCAACACAGGTGA TCACTGTCGGTGCCGGCAGCCAGCACGGCCAAGCCCCCTCCTCTGCCTCGCTCCAACACAGGTGA A G TSC2 Ensembl:ENSG00000103197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2081721..2081817 26863196 MeRIP-seq:(Medium) rs752513898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1661923,Human_Splice_Rec_1662003,Human_Splice_Rec_1662105,Human_Splice_Rec_1662281,Human_Splice_Rec_1662361,Human_Splice_Rec_1662441,Human_Splice_Rec_1662519,Human_Splice_Rec_1662627,Human_Splice_Rec_1662751,Human_Splice_Rec_1662831,Human_Splice_Rec_1662915,Human_Splice_Rec_1662985,Human_Splice_Rec_1663093,Human_Splice_Rec_1663173,Human_Splice_Rec_1663251,Human_Splice_Rec_1663331,Human_Splice_Rec_1663409,Human_Splice_Rec_1663555,Human_Splice_Rec_1663645,Human_Splice_Rec_1663719,Human_Splice_Rec_1663779,Human_Splice_Rec_1663807,Human_Splice_Rec_1663837,Human_Splice_Rec_1663883,Human_Splice_Rec_1663905 RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_82864,RMVar_hsa_circ_81580,RMVar_hsa_circ_175626,RMVar_hsa_circ_175630,RMVar_hsa_circ_110039,RMVar_hsa_circ_175634,RMVar_hsa_circ_105492,RMVar_hsa_circ_121572,RMVar_hsa_circ_175640,RMVar_hsa_circ_103353,RMVar_hsa_circ_175641,RMVar_hsa_circ_175639,RMVar_hsa_circ_2424,RMVar_hsa_circ_35823 72946 RMVar_ID_72946 Human_SNP_ID_591174160 m1A Human chr16 + 2088309 2088292 2088310 CTCCAAGTGGATTGCCCGGCTCCGCCACATCAAGCGGCTCCGCCAGCGGGTAGGGAATATGGGGC CTCCAAGTGGATTGCC__________________CGGCTCCGCCAGCGGGTAGGGAATATGGGGC CCGGCTCCGCCACATCAAG C TSC2 Ensembl:ENSG00000103197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2088262..2088350 26863196 MeRIP-seq:(Medium) rs137854218 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_470166,Human_RBP_ID_26329652 Human_Splice_Rec_1661940,Human_Splice_Rec_1661941,Human_Splice_Rec_1662020,Human_Splice_Rec_1662021,Human_Splice_Rec_1662122,Human_Splice_Rec_1662123,Human_Splice_Rec_1662300,Human_Splice_Rec_1662301,Human_Splice_Rec_1662380,Human_Splice_Rec_1662381,Human_Splice_Rec_1662458,Human_Splice_Rec_1662459,Human_Splice_Rec_1662536,Human_Splice_Rec_1662537,Human_Splice_Rec_1662646,Human_Splice_Rec_1662647,Human_Splice_Rec_1662768,Human_Splice_Rec_1662769,Human_Splice_Rec_1662848,Human_Splice_Rec_1662849,Human_Splice_Rec_1662931,Human_Splice_Rec_1663004,Human_Splice_Rec_1663005,Human_Splice_Rec_1663112,Human_Splice_Rec_1663113,Human_Splice_Rec_1663190,Human_Splice_Rec_1663191,Human_Splice_Rec_1663270,Human_Splice_Rec_1663271,Human_Splice_Rec_1663348,Human_Splice_Rec_1663349,Human_Splice_Rec_1663426,Human_Splice_Rec_1663427,Human_Splice_Rec_1663572,Human_Splice_Rec_1663573,Human_Splice_Rec_1663664,Human_Splice_Rec_1663665,Human_Splice_Rec_1663736,Human_Splice_Rec_1663737,Human_Splice_Rec_1663796,Human_Splice_Rec_1663797,Human_Splice_Rec_1663824,Human_Splice_Rec_1663825,Human_Splice_Rec_1663860,Human_Splice_Rec_1663861,Human_Splice_Rec_1663880,Human_Splice_Rec_1663881,Human_Splice_Rec_1663902,Human_Splice_Rec_1663903,Human_Splice_Rec_1663924,Human_Splice_Rec_1663925,Human_Splice_Rec_1663942,Human_Splice_Rec_1663943,Human_Splice_Rec_1663982,Human_Splice_Rec_1663983 Clinvar_Rec_311 RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_85670,RMVar_hsa_circ_175649 72947 RMVar_ID_72947 Human_SNP_ID_591174178 m1A Human chr16 + 2088309 2088309 2088309 CTCCAAGTGGATTGCCCGGCTCCGCCACATCAAGCGGCTCCGCCAGCGGGTAGGGAATATGGGGC CTCCAAGTGGATTGCCCGGCTCCGCCACATCAGGCGGCTCCGCCAGCGGGTAGGGAATATGGGGC A G TSC2 Ensembl:ENSG00000103197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2088262..2088350 26863196 MeRIP-seq:(Medium) rs753424501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470166,Human_RBP_ID_26329652 Human_Splice_Rec_1661940,Human_Splice_Rec_1661941,Human_Splice_Rec_1662020,Human_Splice_Rec_1662021,Human_Splice_Rec_1662122,Human_Splice_Rec_1662123,Human_Splice_Rec_1662300,Human_Splice_Rec_1662301,Human_Splice_Rec_1662380,Human_Splice_Rec_1662381,Human_Splice_Rec_1662458,Human_Splice_Rec_1662459,Human_Splice_Rec_1662536,Human_Splice_Rec_1662537,Human_Splice_Rec_1662646,Human_Splice_Rec_1662647,Human_Splice_Rec_1662768,Human_Splice_Rec_1662769,Human_Splice_Rec_1662848,Human_Splice_Rec_1662849,Human_Splice_Rec_1662931,Human_Splice_Rec_1663004,Human_Splice_Rec_1663005,Human_Splice_Rec_1663112,Human_Splice_Rec_1663113,Human_Splice_Rec_1663190,Human_Splice_Rec_1663191,Human_Splice_Rec_1663270,Human_Splice_Rec_1663271,Human_Splice_Rec_1663348,Human_Splice_Rec_1663349,Human_Splice_Rec_1663426,Human_Splice_Rec_1663427,Human_Splice_Rec_1663572,Human_Splice_Rec_1663573,Human_Splice_Rec_1663664,Human_Splice_Rec_1663665,Human_Splice_Rec_1663736,Human_Splice_Rec_1663737,Human_Splice_Rec_1663796,Human_Splice_Rec_1663797,Human_Splice_Rec_1663824,Human_Splice_Rec_1663825,Human_Splice_Rec_1663860,Human_Splice_Rec_1663861,Human_Splice_Rec_1663880,Human_Splice_Rec_1663881,Human_Splice_Rec_1663902,Human_Splice_Rec_1663903,Human_Splice_Rec_1663924,Human_Splice_Rec_1663925,Human_Splice_Rec_1663942,Human_Splice_Rec_1663943,Human_Splice_Rec_1663982,Human_Splice_Rec_1663983 RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_85670,RMVar_hsa_circ_175649 72948 RMVar_ID_72948 Human_SNP_ID_591174352 m1A Human chr16 - 2088500 2088500 2088500 GGCTGGAGTCTGTGCAGGGGCTTTGCTATGGGACGGAGGGTGCACCAGAGGTAGGCTGGGGTTGG GGCTGGAGTCTGTGCAGGGGCTTTGCTATGGGCCGGAGGGTGCACCAGAGGTAGGCTGGGGTTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2088426..2088550 26863196 MeRIP-seq:(Medium) rs1060500973 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_312 72949 RMVar_ID_72949 Human_SNP_ID_591174844 m1A Human chr16 + 2088899 2088896 2088900 GCGCGTGCGCGCGCGCACACACACACACACACAGTCACCTTCCTCCACCCTGGGAGCCAGCCCCC GCGCGTGCGCGCGCGCACACACACACACAC____TCACCTTCCTCCACCCTGGGAGCCAGCCCCC CACAG C TSC2 Ensembl:ENSG00000103197 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2088759..2089160 32194978 MeRIP-seq:(Medium) rs201512489 Functional Loss DEL dbSNP153 31..34 33 - - - 72950 RMVar_ID_72950 Human_SNP_ID_591175601 m1A Human chr16 + 2090009 2090009 2090009 GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCAGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCCGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:2089961..2090149;chr16:2089961..2090135 26863196 MeRIP-seq:(Medium) rs7203729 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_313 GWAS_ID_8877,GWAS_ID_8878,GWAS_ID_8879,GWAS_ID_8880,GWAS_ID_8881 72951 RMVar_ID_72951 Human_SNP_ID_591175602 m1A Human chr16 + 2090009 2090009 2090009 GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCAGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCGGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:2089961..2090149;chr16:2089961..2090135 26863196 MeRIP-seq:(Medium) rs7203729 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_313 GWAS_ID_8877,GWAS_ID_8878,GWAS_ID_8879,GWAS_ID_8880,GWAS_ID_8881 72952 RMVar_ID_72952 Human_SNP_ID_591175603 m1A Human chr16 + 2090009 2090009 2090009 GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCAGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT GCCTCGAACACGGCTTGGAGGCGGGAGGGCTCTGGCTCACACCTTGTCCCCAGCCGGCCCAGGCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:2089961..2090149;chr16:2089961..2090135 26863196 MeRIP-seq:(Medium) rs7203729 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_313 GWAS_ID_8877,GWAS_ID_8878,GWAS_ID_8879,GWAS_ID_8880,GWAS_ID_8881 72953 RMVar_ID_72953 Human_SNP_ID_591175610 m1A Human chr16 - 2090023 2090023 2090023 ATGGGCTGAGCGTGAGCCTGGGCCGGCTGGGGACAAGGTGTGAGCCTGAGCCCTCCCGCCTCCAA ATGGGCTGAGCGTGAGCCTGGGCCGGCTGGGGTCAAGGTGTGAGCCTGAGCCCTCCCGCCTCCAA T A PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2089976..2090025 26863196 MeRIP-seq:(Medium) rs1342963250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8805477 Human_miRNA_ID_2257987,Human_miRNA_ID_2269993,Human_miRNA_ID_2450772 RMVar_hsa_circ_96170,RMVar_hsa_circ_175651 72954 RMVar_ID_72954 Human_SNP_ID_591179943 m1A Human chr16 - 2097323 2097323 2097323 AGCCCCTACTCGCCTGCCAAATCCTTCTCAGCATCAGGTGAGCTGGGGTGAGAGGAGGGGGCTCT AGCCCCTACTCGCCTGCCAAATCCTTCTCAGCTTCAGGTGAGCTGGGGTGAGAGGAGGGGGCTCT T A PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2097318..2097419 32194978 MeRIP-seq:(Medium) rs200899577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1664057,Human_Splice_Rec_1664147,Human_Splice_Rec_1664225 RMVar_hsa_circ_4287,RMVar_hsa_circ_96170,RMVar_hsa_circ_175651,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_94914,RMVar_hsa_circ_175652,RMVar_hsa_circ_175653,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_113945,RMVar_hsa_circ_97207,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175663,RMVar_hsa_circ_175664,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660 72955 RMVar_ID_72955 Human_SNP_ID_591179944 m1A Human chr16 - 2097323 2097323 2097323 AGCCCCTACTCGCCTGCCAAATCCTTCTCAGCATCAGGTGAGCTGGGGTGAGAGGAGGGGGCTCT AGCCCCTACTCGCCTGCCAAATCCTTCTCAGCGTCAGGTGAGCTGGGGTGAGAGGAGGGGGCTCT T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2097318..2097419 32194978 MeRIP-seq:(Medium) rs200899577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1664057,Human_Splice_Rec_1664147,Human_Splice_Rec_1664225 RMVar_hsa_circ_4287,RMVar_hsa_circ_96170,RMVar_hsa_circ_175651,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_94914,RMVar_hsa_circ_175652,RMVar_hsa_circ_175653,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_113945,RMVar_hsa_circ_97207,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175663,RMVar_hsa_circ_175664,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660 72956 RMVar_ID_72956 Human_SNP_ID_591180053 m1A Human chr16 + 2097471 2097471 2097471 TGGACGGGTCACTGAGCAGGTCCGGCCAACTGAGCGTTCCCTCGCCGGAGGGCCAGCACACCAGA TGGACGGGTCACTGAGCAGGTCCGGCCAACTGGGCGTTCCCTCGCCGGAGGGCCAGCACACCAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2097423..2097500 26863196 MeRIP-seq:(Medium) rs1361916151 Functional Loss SNV dbSNP153 33..33 33 - - - 72957 RMVar_ID_72957 Human_SNP_ID_591181947 m1A Human chr16 + 2100875 2100875 2100875 ACCCGCACTGCACACCTGTCCACGCCTCAGTCATGCCACAACCGGTGACCCGCACCACACACCCG ACCCGCACTGCACACCTGTCCACGCCTCAGTCGTGCCACAACCGGTGACCCGCACCACACACCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2100866..2100935 26863196 MeRIP-seq:(Medium) rs1226457211 Functional Loss SNV dbSNP153 33..33 33 - - - 72958 RMVar_ID_72958 Human_SNP_ID_591185029 m1A Human chr16 - 2105937 2105937 2105937 TGGCTGCACGGGCTCACCGCTAGTGTGCTCCCAGGGCTGCTGCGGCAGGCCGATCCCCAGCACGT TGGCTGCACGGGCTCACCGCTAGTGTGCTCCCGGGGCTGCTGCGGCAGGCCGATCCCCAGCACGT T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2105831..2106148 32194978 MeRIP-seq:(Medium) rs566533475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233057,Human_RBP_ID_470180,Human_RBP_ID_815779,Human_RBP_ID_3947112,Human_RBP_ID_20102260,Human_RBP_ID_27439907 Human_Splice_Rec_1664030,Human_Splice_Rec_1664031,Human_Splice_Rec_1664120,Human_Splice_Rec_1664121,Human_Splice_Rec_1664196,Human_Splice_Rec_1664197,Human_Splice_Rec_1664312,Human_Splice_Rec_1664342,Human_Splice_Rec_1664343,Human_Splice_Rec_1664378,Human_Splice_Rec_1664379,Human_Splice_Rec_1664414,Human_Splice_Rec_1664415,Human_Splice_Rec_1664494,Human_Splice_Rec_1664495,Human_Splice_Rec_1664516,Human_Splice_Rec_1664517,Human_Splice_Rec_1664524,Human_Splice_Rec_1664525,Human_Splice_Rec_1664528,Human_Splice_Rec_1664529 RMVar_hsa_circ_4287,RMVar_hsa_circ_96170,RMVar_hsa_circ_175651,RMVar_hsa_circ_78931,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_94914,RMVar_hsa_circ_175652,RMVar_hsa_circ_175653,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_105190,RMVar_hsa_circ_175668,RMVar_hsa_circ_175669,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_108008,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_322403,RMVar_hsa_circ_175675,RMVar_hsa_circ_126891,RMVar_hsa_circ_175677,RMVar_hsa_circ_175678,RMVar_hsa_circ_175676 72959 RMVar_ID_72959 Human_SNP_ID_591187504 m1A Human chr16 + 2109590 2109590 2109590 TTGGAGGCATTGAGCCGGATGGAGAAGGTGCCAGCATCCGGGAAGACCATGGTGACATGAGGGCC TTGGAGGCATTGAGCCGGATGGAGAAGGTGCCGGCATCCGGGAAGACCATGGTGACATGAGGGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2109589..2109690 32194978 MeRIP-seq:(Medium) rs140662778 Functional Loss SNV dbSNP153 33..33 33 - - - 72960 RMVar_ID_72960 Human_SNP_ID_591187849 m1A Human chr16 + 2110107 2110107 2110107 GCAGCTGCACATGGTAGGTGCCGGCCTCGAGCACGGTGAGCGAGAAGCCTTTGCCGCTGCCGGCC GCAGCTGCACATGGTAGGTGCCGGCCTCGAGCGCGGTGAGCGAGAAGCCTTTGCCGCTGCCGGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2109789..2110240 32194978 MeRIP-seq:(Medium) rs773158372 Functional Loss SNV dbSNP153 33..33 33 - - - 72961 RMVar_ID_72961 Human_SNP_ID_591188017 m1A Human chr16 - 2110339 2110336 2110339 ACACCTTCCGCTCCGTGGGCACCTTCAATATCATCGTCACGGCTGAGAACGAGGTGGGCTCCGCC ACACCTTCCGCTCCGTGGGCACCTTCAATATC___GTCACGGCTGAGAACGAGGTGGGCTCCGCC CGAT C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2110303..2110458 26863196 MeRIP-seq:(Medium) rs1567198691 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_233064,Human_RBP_ID_470185,Human_RBP_ID_3948554,Human_RBP_ID_5317308,Human_RBP_ID_5523940,Human_RBP_ID_8429290,Human_RBP_ID_18189805,Human_RBP_ID_18469879,Human_RBP_ID_26940059,Human_RBP_ID_27439918 RMVar_hsa_circ_78931,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_175652,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_93136,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_105190,RMVar_hsa_circ_175668,RMVar_hsa_circ_175669,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_126891,RMVar_hsa_circ_120064,RMVar_hsa_circ_175677,RMVar_hsa_circ_175678,RMVar_hsa_circ_110879,RMVar_hsa_circ_175679,RMVar_hsa_circ_175680,RMVar_hsa_circ_175682,RMVar_hsa_circ_89411,RMVar_hsa_circ_175681,RMVar_hsa_circ_121452,RMVar_hsa_circ_175683 72962 RMVar_ID_72962 Human_SNP_ID_591188022 m1A Human chr16 - 2110339 2110339 2110339 ACACCTTCCGCTCCGTGGGCACCTTCAATATCATCGTCACGGCTGAGAACGAGGTGGGCTCCGCC ACACCTTCCGCTCCGTGGGCACCTTCAATATCGTCGTCACGGCTGAGAACGAGGTGGGCTCCGCC T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2110303..2110458 26863196 MeRIP-seq:(Medium) rs1033000422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233064,Human_RBP_ID_470185,Human_RBP_ID_3948554,Human_RBP_ID_5317308,Human_RBP_ID_5523940,Human_RBP_ID_8429290,Human_RBP_ID_18189805,Human_RBP_ID_18469879,Human_RBP_ID_26940059,Human_RBP_ID_27439918 RMVar_hsa_circ_78931,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_175652,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_93136,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_105190,RMVar_hsa_circ_175668,RMVar_hsa_circ_175669,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_126891,RMVar_hsa_circ_120064,RMVar_hsa_circ_175677,RMVar_hsa_circ_175678,RMVar_hsa_circ_110879,RMVar_hsa_circ_175679,RMVar_hsa_circ_175680,RMVar_hsa_circ_175682,RMVar_hsa_circ_89411,RMVar_hsa_circ_175681,RMVar_hsa_circ_121452,RMVar_hsa_circ_175683 72963 RMVar_ID_72963 Human_SNP_ID_591188644 m1A Human chr16 + 2111270 2111270 2111270 TCAGGCTGCGTGGGGATGCAGGCGGCGGGTTCAACGCGCAGCACCTCCAGGACGAAGACCAGCAC TCAGGCTGCGTGGGGATGCAGGCGGCGGGTTCCACGCGCAGCACCTCCAGGACGAAGACCAGCAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2111038..2111488 32194978 MeRIP-seq:(Medium) rs567722956 Functional Loss SNV dbSNP153 33..33 33 - - - 72964 RMVar_ID_72964 Human_SNP_ID_591188645 m1A Human chr16 + 2111270 2111270 2111270 TCAGGCTGCGTGGGGATGCAGGCGGCGGGTTCAACGCGCAGCACCTCCAGGACGAAGACCAGCAC TCAGGCTGCGTGGGGATGCAGGCGGCGGGTTCGACGCGCAGCACCTCCAGGACGAAGACCAGCAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2111038..2111488 32194978 MeRIP-seq:(Medium) rs567722956 Functional Loss SNV dbSNP153 33..33 33 - - - 72965 RMVar_ID_72965 Human_SNP_ID_591188788 m1A Human chr16 - 2111473 2111473 2111473 TGGCCGTGGAGCAGGGCGCCCCCGTGGTGGTCAGCGCCGCGGTGCAGACGGGCGACAACATCACG TGGCCGTGGAGCAGGGCGCCCCCGTGGTGGTCGGCGCCGCGGTGCAGACGGGCGACAACATCACG T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2111437..2111535 26863196 MeRIP-seq:(Medium) rs1267051267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5621,Human_RBP_ID_233068,Human_RBP_ID_889332,Human_RBP_ID_5523948,Human_RBP_ID_18189809,Human_RBP_ID_23256412 RMVar_hsa_circ_78931,RMVar_hsa_circ_110337,RMVar_hsa_circ_78828,RMVar_hsa_circ_175652,RMVar_hsa_circ_86481,RMVar_hsa_circ_120480,RMVar_hsa_circ_175655,RMVar_hsa_circ_175656,RMVar_hsa_circ_123053,RMVar_hsa_circ_175657,RMVar_hsa_circ_103321,RMVar_hsa_circ_175658,RMVar_hsa_circ_175659,RMVar_hsa_circ_81953,RMVar_hsa_circ_96805,RMVar_hsa_circ_91522,RMVar_hsa_circ_175661,RMVar_hsa_circ_175662,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_93136,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_105190,RMVar_hsa_circ_175668,RMVar_hsa_circ_175669,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_126891,RMVar_hsa_circ_120064,RMVar_hsa_circ_175677,RMVar_hsa_circ_175678,RMVar_hsa_circ_110879,RMVar_hsa_circ_175679,RMVar_hsa_circ_175680,RMVar_hsa_circ_175682,RMVar_hsa_circ_89411,RMVar_hsa_circ_175681,RMVar_hsa_circ_121452,RMVar_hsa_circ_175683 72966 RMVar_ID_72966 Human_SNP_ID_591189689 m1A Human chr16 + 2112869 2112869 2112869 CTAGCGTGGCATTGGGGGACAGCACGGCCGGCACTGTGGAGACCTGCAGACCCTGCATCCTGTTC CTAGCGTGGCATTGGGGGACAGCACGGCCGGCCCTGTGGAGACCTGCAGACCCTGCATCCTGTTC A C AC009065.7 Ensembl:ENSG00000261240 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2112819..2112920 32194978 MeRIP-seq:(Medium) rs377725958 Functional Loss SNV dbSNP153 33..33 33 - - - 72967 RMVar_ID_72967 Human_SNP_ID_591189965 m1A Human chr16 - 2113292 2113292 2113292 CAGAGCCCAGGCTGACACCATTCCCCCCGCAGAGGTACAGCCCCGTGGTGGAGGCCGGCTCGGAC CAGAGCCCAGGCTGACACCATTCCCCCCGCAGGGGTACAGCCCCGTGGTGGAGGCCGGCTCGGAC T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2113250..2113839 32194978 MeRIP-seq:(Medium) rs765416384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815927,Human_RBP_ID_888306,Human_RBP_ID_5523950,Human_RBP_ID_18189810,Human_RBP_ID_18469641,Human_RBP_ID_18985188,Human_RBP_ID_22651491,Human_RBP_ID_22738160 Human_Splice_Rec_1664014,Human_Splice_Rec_1664104,Human_Splice_Rec_1664366,Human_Splice_Rec_1664502,Human_Splice_Rec_1664550 RMVar_hsa_circ_96805,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_93136,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_120064,RMVar_hsa_circ_175678,RMVar_hsa_circ_175679,RMVar_hsa_circ_175682,RMVar_hsa_circ_89411,RMVar_hsa_circ_175681,RMVar_hsa_circ_121452,RMVar_hsa_circ_175683,RMVar_hsa_circ_101621,RMVar_hsa_circ_175685 72968 RMVar_ID_72968 Human_SNP_ID_591189966 m1A Human chr16 - 2113292 2113292 2113292 CAGAGCCCAGGCTGACACCATTCCCCCCGCAGAGGTACAGCCCCGTGGTGGAGGCCGGCTCGGAC CAGAGCCCAGGCTGACACCATTCCCCCCGCAGCGGTACAGCCCCGTGGTGGAGGCCGGCTCGGAC T G PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2113250..2113839 32194978 MeRIP-seq:(Medium) rs765416384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815927,Human_RBP_ID_888306,Human_RBP_ID_5523950,Human_RBP_ID_18189810,Human_RBP_ID_18469641,Human_RBP_ID_18985188,Human_RBP_ID_22651491,Human_RBP_ID_22738160 Human_Splice_Rec_1664014,Human_Splice_Rec_1664104,Human_Splice_Rec_1664366,Human_Splice_Rec_1664502,Human_Splice_Rec_1664550 RMVar_hsa_circ_96805,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_93136,RMVar_hsa_circ_90105,RMVar_hsa_circ_96020,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175674,RMVar_hsa_circ_120064,RMVar_hsa_circ_175678,RMVar_hsa_circ_175679,RMVar_hsa_circ_175682,RMVar_hsa_circ_89411,RMVar_hsa_circ_175681,RMVar_hsa_circ_121452,RMVar_hsa_circ_175683,RMVar_hsa_circ_101621,RMVar_hsa_circ_175685 72969 RMVar_ID_72969 Human_SNP_ID_591191851 m1A Human chr16 - 2116841 2116841 2116841 CTCAGCGCCGCACAGCTACGTCTGCGAGCTGCAGCCCGGAGGTGTGCGGGGGGCCAGGCAGGGGC CTCAGCGCCGCACAGCTACGTCTGCGAGCTGCGGCCCGGAGGTGTGCGGGGGGCCAGGCAGGGGC T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2116100..2116899 32194978 MeRIP-seq:(Medium) rs2855342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891253,Human_RBP_ID_3947132,Human_RBP_ID_18983030 Human_Splice_Rec_1664005,Human_Splice_Rec_1664095,Human_Splice_Rec_1664541 RMVar_hsa_circ_96805,RMVar_hsa_circ_175660,RMVar_hsa_circ_175667,RMVar_hsa_circ_89252,RMVar_hsa_circ_96020,RMVar_hsa_circ_113821,RMVar_hsa_circ_175670,RMVar_hsa_circ_175672,RMVar_hsa_circ_106135,RMVar_hsa_circ_92028,RMVar_hsa_circ_175673,RMVar_hsa_circ_175678,RMVar_hsa_circ_101621,RMVar_hsa_circ_175685,RMVar_hsa_circ_122165,RMVar_hsa_circ_175687 72970 RMVar_ID_72970 Human_SNP_ID_591193867 m1A Human chr16 + 2121801 2121801 2121801 TGCACACCACCCCCCTGCTCCCCAGGACCCCGAGGCCTCACCTCCTGCCACGGGCCTCTACTTCC TGCACACCACCCCCCTGCTCCCCAGGACCCCGGGGCCTCACCTCCTGCCACGGGCCTCTACTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2121762..2121955 26863196 MeRIP-seq:(Medium) rs1175836640 Functional Loss SNV dbSNP153 33..33 33 - - - 72971 RMVar_ID_72971 Human_SNP_ID_591193873 m1A Human chr16 - 2121806 2121806 2121806 CCTGGGGAAGTAGAGGCCCGTGGCAGGAGGTGAGGCCTCGGGGTCCTGGGGAGCAGGGGGGTGGT CCTGGGGAAGTAGAGGCCCGTGGCAGGAGGTGTGGCCTCGGGGTCCTGGGGAGCAGGGGGGTGGT T A PKD1 Ensembl:ENSG00000008710 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:2121772..2121919;chr16:2121706..2122003;chr16:2121642..2122018 26863196 MeRIP-seq:(Medium) rs1480550898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8184199 RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 72972 RMVar_ID_72972 Human_SNP_ID_591198349 m1A Human chr16 - 2135242 2135242 2135242 CTGGAGACAGACGTCCCACCCGGGGGCTCTGCAGACGCCAGCGGGGGCGGGGCGCGGAGGCCGCG CTGGAGACAGACGTCCCACCCGGGGGCTCTGCGGACGCCAGCGGGGGCGGGGCGCGGAGGCCGCG T C PKD1 Ensembl:ENSG00000008710 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2135221..2135375 26863196 MeRIP-seq:(Medium) rs1226365861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 72973 RMVar_ID_72973 Human_SNP_ID_591198486 m1A Human chr16 - 2135567 2135567 2135567 GGGCCCTGCGAGCCCCCCTGCCTCTGCGGCCCAGCGCCCGGCGCCGCCTGCCGCGTCAACTGCTC GGGCCCTGCGAGCCCCCCTGCCTCTGCGGCCCGGCGCCCGGCGCCGCCTGCCGCGTCAACTGCTC T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2135467..2135593 26863196 MeRIP-seq:(Medium) rs1255231202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392770,Human_RBP_ID_17873162,Human_RBP_ID_26780064 Human_Splice_Rec_1663993,Human_Splice_Rec_1664083 RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 72974 RMVar_ID_72974 Human_SNP_ID_591198607 m1A Human chr16 + 2135881 2135881 2135881 AGGCCGCTCCGGGAGCTCGGCCGCCCGCTCGGACGCTGGCGCTGCAGTGCGGGCCCCGCCGCGGC AGGCCGCTCCGGGAGCTCGGCCGCCCGCTCGGCCGCTGGCGCTGCAGTGCGGGCCCCGCCGCGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2135820..2135906 26863196 MeRIP-seq:(Medium) rs1473931159 Functional Loss SNV dbSNP153 33..33 33 - - - 72975 RMVar_ID_72975 Human_SNP_ID_591202845 m1A Human chr16 - 2148711 2148711 2148711 GCCCTGGGCCGTCCCGCACCCCGCGCCCGCCGAGCCCGACCCGGACCCGAACCCTTCCCCTGGCG GCCCTGGGCCGTCCCGCACCCCGCGCCCGCCGGGCCCGACCCGGACCCGAACCCTTCCCCTGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2148626..2150011 26863196 MeRIP-seq:(Medium) rs1324033271 Functional Loss SNV dbSNP153 33..33 33 - - - 72976 RMVar_ID_72976 Human_SNP_ID_591202854 m1A Human chr16 + 2148732 2148732 2148732 CCGGGTCGGGCTCGGCGGGCGCGGGGTGCGGGACGGCCCAGGGCACGGCGGCTGCAGCGGGAGCA CCGGGTCGGGCTCGGCGGGCGCGGGGTGCGGGGCGGCCCAGGGCACGGCGGCTGCAGCGGGAGCA A G RAB26 Ensembl:ENSG00000167964 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2148685..2148829 26863196 MeRIP-seq:(Medium) rs907275969 Functional Loss SNV dbSNP153 33..33 33 - - - 72977 RMVar_ID_72977 Human_SNP_ID_591203995 m1A Human chr16 - 2151760 2151760 2151760 CCCCAACCAGCCCAGGTACCCAGGGGCTCACCATGAGCATCCCGGTAGTAGGCATGGGTAACACT CCCCAACCAGCCCAGGTACCCAGGGGCTCACCGTGAGCATCCCGGTAGTAGGCATGGGTAACACT T C SNHG19 RNACentral:URS0000D5A510 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2151750..2151840 26863196 MeRIP-seq:(Medium) rs377196029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12687006,Human_RBP_ID_18674821 72978 RMVar_ID_72978 Human_SNP_ID_591205703 m1A Human chr16 + 2155295 2155295 2155295 CTCAAAGCCACGCTCGTGGCTCAGTTCGTCCCAAGATCGTAGCACATGGCGAACGTATTAACAAA CTCAAAGCCACGCTCGTGGCTCAGTTCGTCCCGAGATCGTAGCACATGGCGAACGTATTAACAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2155176..2155350 26863196 MeRIP-seq:(Medium) rs1020434704 Functional Loss SNV dbSNP153 33..33 33 - - - 72979 RMVar_ID_72979 Human_SNP_ID_591205707 m1A Human chr16 - 2155302 2155302 2155302 GAAGAGGTTTGTTAATACGTTCGCCATGTGCTACGATCTTGGGACGAACTGAGCCACGAGCGTGG GAAGAGGTTTGTTAATACGTTCGCCATGTGCTGCGATCTTGGGACGAACTGAGCCACGAGCGTGG T C SNHG19 Ensembl:ENSG00000260260 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2155126..2155350 26863196 MeRIP-seq:(Medium) rs1311976751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470331,Human_RBP_ID_1281286,Human_RBP_ID_1365191,Human_RBP_ID_1514068,Human_RBP_ID_1839410,Human_RBP_ID_3510931,Human_RBP_ID_4355716,Human_RBP_ID_5113311,Human_RBP_ID_5576614,Human_RBP_ID_8429474,Human_RBP_ID_12687872,Human_RBP_ID_18162016,Human_RBP_ID_18418639,Human_RBP_ID_18674847,Human_RBP_ID_22054438,Human_RBP_ID_22198148,Human_RBP_ID_23682457,Human_RBP_ID_26940173 72980 RMVar_ID_72980 Human_SNP_ID_591205710 m1A Human chr16 + 2155306 2155306 2155306 GCTCGTGGCTCAGTTCGTCCCAAGATCGTAGCACATGGCGAACGTATTAACAAACCTCTTCCCCC GCTCGTGGCTCAGTTCGTCCCAAGATCGTAGCTCATGGCGAACGTATTAACAAACCTCTTCCCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2155126..2155350 26863196 MeRIP-seq:(Medium) rs559354217 Functional Loss SNV dbSNP153 33..33 33 - - - 72981 RMVar_ID_72981 Human_SNP_ID_591205713 m1A Human chr16 - 2155309 2155309 2155309 CGAGGGGGAAGAGGTTTGTTAATACGTTCGCCATGTGCTACGATCTTGGGACGAACTGAGCCACG CGAGGGGGAAGAGGTTTGTTAATACGTTCGCCTTGTGCTACGATCTTGGGACGAACTGAGCCACG T A SNHG19 Ensembl:ENSG00000260260 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2155276..2155350 26863196 MeRIP-seq:(Medium) rs528443881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470332,Human_RBP_ID_1281286,Human_RBP_ID_1514068,Human_RBP_ID_1839410,Human_RBP_ID_4355717,Human_RBP_ID_12687872,Human_RBP_ID_18162016,Human_RBP_ID_18418640,Human_RBP_ID_18674847,Human_RBP_ID_22054438,Human_RBP_ID_22198148,Human_RBP_ID_23682458 72982 RMVar_ID_72982 Human_SNP_ID_591205714 m1A Human chr16 - 2155309 2155309 2155309 CGAGGGGGAAGAGGTTTGTTAATACGTTCGCCATGTGCTACGATCTTGGGACGAACTGAGCCACG CGAGGGGGAAGAGGTTTGTTAATACGTTCGCCGTGTGCTACGATCTTGGGACGAACTGAGCCACG T C SNHG19 Ensembl:ENSG00000260260 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2155276..2155350 26863196 MeRIP-seq:(Medium) rs528443881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470332,Human_RBP_ID_1281286,Human_RBP_ID_1514068,Human_RBP_ID_1839410,Human_RBP_ID_4355717,Human_RBP_ID_12687872,Human_RBP_ID_18162016,Human_RBP_ID_18418640,Human_RBP_ID_18674847,Human_RBP_ID_22054438,Human_RBP_ID_22198148,Human_RBP_ID_23682458 72983 RMVar_ID_72983 Human_SNP_ID_591205990 m1A Human chr16 - 2155833 2155833 2155833 CACTCACCCGCCCGCGGCCGCCCGGGAGCGGCAGCGCCGCCAGCCCGCTTCATGATGCCCCCTCG CACTCACCCGCCCGCGGCCGCCCGGGAGCGGCCGCGCCGCCAGCCCGCTTCATGATGCCCCCTCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2155776..2155928 26863196 MeRIP-seq:(Medium) rs1010455717 Functional Loss SNV dbSNP153 33..33 33 - - - 72984 RMVar_ID_72984 Human_SNP_ID_591208724 m1A Human chr16 - 2163823 2163823 2163823 TGAGAGATGGAGCCCAGGCCCCTGTGAGTCAGACGGGCTGCTGCAAGTGTGCAGACCTGCTGTGG TGAGAGATGGAGCCCAGGCCCCTGTGAGTCAGTCGGGCTGCTGCAAGTGTGCAGACCTGCTGTGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2163818..2164025 26863410 MeRIP-seq:(Medium) rs1490627924 Functional Loss SNV dbSNP153 33..33 33 - - - 72985 RMVar_ID_72985 Human_SNP_ID_591208770 m1A Human chr16 + 2163949 2163949 2163949 GAGCATGAGCTCAGGCAAGAGTGCCCGCTACAACCGCTTCTCCGGGGGGCCCAGCAATCTTCCCA GAGCATGAGCTCAGGCAAGAGTGCCCGCTACAGCCGCTTCTCCGGGGGGCCCAGCAATCTTCCCA A G TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2163901..2163975 32194978 MeRIP-seq:(Medium) rs1567246901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233633,Human_RBP_ID_4393495,Human_RBP_ID_18189813 Human_Splice_Rec_1664712,Human_Splice_Rec_1664713,Human_Splice_Rec_1664718,Human_Splice_Rec_1664719,Human_Splice_Rec_1664728,Human_Splice_Rec_1664729,Human_Splice_Rec_1664768,Human_Splice_Rec_1664769,Human_Splice_Rec_1664774,Human_Splice_Rec_1664775,Human_Splice_Rec_1664790,Human_Splice_Rec_1664791 RMVar_hsa_circ_888,RMVar_hsa_circ_46109,RMVar_hsa_circ_87998,RMVar_hsa_circ_175695 72986 RMVar_ID_72986 Human_SNP_ID_591208788 m1A Human chr16 - 2163976 2163976 2163976 CCCTTACCCCTGTGGTGACGTCTGGGGTGGGAAGATTGCTGGGCCCCCCGGAGAAGCGGTTGTAG CCCTTACCCCTGTGGTGACGTCTGGGGTGGGATGATTGCTGGGCCCCCCGGAGAAGCGGTTGTAG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2163926..2164000;chr16:2163926..2164025 26863196 MeRIP-seq:(Medium) rs766923754 Functional Loss SNV dbSNP153 33..33 33 - - - 72987 RMVar_ID_72987 Human_SNP_ID_591208789 m1A Human chr16 - 2163976 2163976 2163976 CCCTTACCCCTGTGGTGACGTCTGGGGTGGGAAGATTGCTGGGCCCCCCGGAGAAGCGGTTGTAG CCCTTACCCCTGTGGTGACGTCTGGGGTGGGAGGATTGCTGGGCCCCCCGGAGAAGCGGTTGTAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2163926..2164000;chr16:2163926..2164025 26863196 MeRIP-seq:(Medium) rs766923754 Functional Loss SNV dbSNP153 33..33 33 - - - 72988 RMVar_ID_72988 Human_SNP_ID_591210031 m1A Human chr16 + 2165882 2165882 2165882 AGGCCAGGTCTCCTCCGTCCTCCCTCTAGACCAGAATGGAAACGACCTTCGGACCCGCCTTTTCA AGGCCAGGTCTCCTCCGTCCTCCCTCTAGACCGGAATGGAAACGACCTTCGGACCCGCCTTTTCA A G TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2165876..2165950 26863196 MeRIP-seq:(Medium) rs77497016 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_761294,Human_RBP_ID_5357410,Human_RBP_ID_5646745,Human_RBP_ID_9325776,Human_RBP_ID_22583588,Human_RBP_ID_26809852 Human_Splice_Rec_1664714,Human_Splice_Rec_1664715,Human_Splice_Rec_1664720,Human_Splice_Rec_1664721,Human_Splice_Rec_1664730,Human_Splice_Rec_1664731,Human_Splice_Rec_1664770,Human_Splice_Rec_1664771,Human_Splice_Rec_1664776,Human_Splice_Rec_1664777,Human_Splice_Rec_1664792,Human_Splice_Rec_1664793 Human_miRNA_ID_2728071 RMVar_hsa_circ_888,RMVar_hsa_circ_46109,RMVar_hsa_circ_87998,RMVar_hsa_circ_90242,RMVar_hsa_circ_115814,RMVar_hsa_circ_20899,RMVar_hsa_circ_175695,RMVar_hsa_circ_124813,RMVar_hsa_circ_105643,RMVar_hsa_circ_175696,RMVar_hsa_circ_175698,RMVar_hsa_circ_175699,RMVar_hsa_circ_175697 72989 RMVar_ID_72989 Human_SNP_ID_591211451 m1A Human chr16 - 2170553 2170553 2170553 GGGCTCCGCACGGGGTCAGAGCCTCGGGGAGGACAGGACCCAGCCCGGCGGAAGCGCGAGGGCAG GGGCTCCGCACGGGGTCAGAGCCTCGGGGAGGGCAGGACCCAGCCCGGCGGAAGCGCGAGGGCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2170551..2170640 26863196 MeRIP-seq:(Medium) rs1468994593 Functional Loss SNV dbSNP153 33..33 33 - - - 72990 RMVar_ID_72990 Human_SNP_ID_591211457 m1A Human chr16 - 2170566 2170566 2170566 GGCGCCTGTCGGGGGGCTCCGCACGGGGTCAGAGCCTCGGGGAGGACAGGACCCAGCCCGGCGGA GGCGCCTGTCGGGGGGCTCCGCACGGGGTCAGGGCCTCGGGGAGGACAGGACCCAGCCCGGCGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2170563..2170769 26863196 MeRIP-seq:(Medium) rs761745252 Functional Loss SNV dbSNP153 33..33 33 - - - 72991 RMVar_ID_72991 Human_SNP_ID_591212145 m1A Human chr16 + 2172310 2172310 2172310 GCCGGCACGGCTGCCGGGTAGCGGGCAGCGGGAAGCCCCCCATCTTTGAGGTGGACCCCCGAGGG GCCGGCACGGCTGCCGGGTAGCGGGCAGCGGGCAGCCCCCCATCTTTGAGGTGGACCCCCGAGGG A C TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2170703..2173281 32194978 MeRIP-seq:(Medium) rs1390431572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9325777,Human_RBP_ID_18189818,Human_RBP_ID_18469647 Human_Splice_Rec_1664741,Human_Splice_Rec_1664787 RMVar_hsa_circ_888,RMVar_hsa_circ_87998,RMVar_hsa_circ_26539,RMVar_hsa_circ_90242,RMVar_hsa_circ_115814,RMVar_hsa_circ_175695,RMVar_hsa_circ_105643,RMVar_hsa_circ_175698,RMVar_hsa_circ_175699,RMVar_hsa_circ_175697,RMVar_hsa_circ_107870,RMVar_hsa_circ_112294,RMVar_hsa_circ_175701,RMVar_hsa_circ_110851,RMVar_hsa_circ_105286,RMVar_hsa_circ_123786,RMVar_hsa_circ_175702,RMVar_hsa_circ_175703,RMVar_hsa_circ_175704,RMVar_hsa_circ_175707,RMVar_hsa_circ_76905,RMVar_hsa_circ_175706 72992 RMVar_ID_72992 Human_SNP_ID_591212600 m1A Human chr16 + 2173510 2173510 2173510 CAGACGTCCTGGACGAAAACCAGAGCAAGCTCAGCGAGGACCTCATGGAGTTCCGGCGGGACGCA CAGACGTCCTGGACGAAAACCAGAGCAAGCTCGGCGAGGACCTCATGGAGTTCCGGCGGGACGCA A G TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2173380..2173795 32194978 MeRIP-seq:(Medium) rs1290697399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889339,Human_RBP_ID_3947144,Human_RBP_ID_9060919,Human_RBP_ID_18983038,Human_RBP_ID_23682602,Human_RBP_ID_27811484 Human_Splice_Rec_1664746,Human_Splice_Rec_1664747,Human_Splice_Rec_1664799 RMVar_hsa_circ_888,RMVar_hsa_circ_90242,RMVar_hsa_circ_115814,RMVar_hsa_circ_175698,RMVar_hsa_circ_175699,RMVar_hsa_circ_107870,RMVar_hsa_circ_112294,RMVar_hsa_circ_175701,RMVar_hsa_circ_105286,RMVar_hsa_circ_123786,RMVar_hsa_circ_175703,RMVar_hsa_circ_175704,RMVar_hsa_circ_29453,RMVar_hsa_circ_175707,RMVar_hsa_circ_76905,RMVar_hsa_circ_175706 72993 RMVar_ID_72993 Human_SNP_ID_591213307 m1A Human chr16 + 2175352 2175343 2175353 TGCAGAAGGTGAACACCATCCGGGCCCATGACAACCCGGTGTGCACGCTGGTCTCCTCACACAAC TGCAGAAGGTGAACACCATCCGGG__________CCCGGTGTGCACGCTGGTCTCCTCACACAAC GCCCATGACAA G TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2175156..2177879 32194978 MeRIP-seq:(Medium) rs1415968555 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_1365204,Human_RBP_ID_17689829,Human_RBP_ID_17873278 Human_Splice_Rec_1664756,Human_Splice_Rec_1664757 RMVar_hsa_circ_888,RMVar_hsa_circ_90242,RMVar_hsa_circ_175699,RMVar_hsa_circ_52420,RMVar_hsa_circ_105286,RMVar_hsa_circ_29453,RMVar_hsa_circ_175707,RMVar_hsa_circ_82874,RMVar_hsa_circ_175709,RMVar_hsa_circ_93065,RMVar_hsa_circ_175711,RMVar_hsa_circ_76948,RMVar_hsa_circ_108107,RMVar_hsa_circ_175710,RMVar_hsa_circ_87336,RMVar_hsa_circ_175712,RMVar_hsa_circ_175713 72994 RMVar_ID_72994 Human_SNP_ID_591213938 m1A Human chr16 - 2176941 2176941 2176941 CCCCCTTGTCCCGAGGAGCTGTCCCCACTCACAGCCACAGTCTGTGGAGCATTTATTTCAACCAG CCCCCTTGTCCCGAGGAGCTGTCCCCACTCACTGCCACAGTCTGTGGAGCATTTATTTCAACCAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2176899..2176989 26863196 MeRIP-seq:(Medium) rs777883683 Functional Loss SNV dbSNP153 33..33 33 - - - 72995 RMVar_ID_72995 Human_SNP_ID_591214018 m1A Human chr16 - 2177192 2177192 2177192 GGGCAAGGCGCTGCCGTCGGCTGTCAATAAACAGCAGGAAACAGAGGTGCCTGGCTCACTTTTTG GGGCAAGGCGCTGCCGTCGGCTGTCAATAAACGGCAGGAAACAGAGGTGCCTGGCTCACTTTTTG T C CASKIN1 Ensembl:ENSG00000167971 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2177176..2177250 26863196 MeRIP-seq:(Medium) rs1254416957 Functional Loss SNV dbSNP153 33..33 33 - - - 72996 RMVar_ID_72996 Human_SNP_ID_591220426 m1A Human chr16 - 2192549 2192549 2192549 GTGCACACAGGGCATGTGGAAAGGCCTTGGACAGGGCAGCCGATATGTTGGAGGAACGTCTGGAG GTGCACACAGGGCATGTGGAAAGGCCTTGGACGGGGCAGCCGATATGTTGGAGGAACGTCTGGAG T C CASKIN1 Ensembl:ENSG00000167971 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2192547..2192698 26863196 MeRIP-seq:(Medium) rs951382034 Functional Loss SNV dbSNP153 33..33 33 - - - 72997 RMVar_ID_72997 Human_SNP_ID_591224624 m1A Human chr16 - 2205777 2205777 2205777 CCCCCCACCTCCGCAGCCGGCAGGGGGGAGTCACGCGCGGGCGCCACTCTGCCGCAGGGGCGGGC CCCCCCACCTCCGCAGCCGGCAGGGGGGAGTCGCGCGCGGGCGCCACTCTGCCGCAGGGGCGGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2205768..2205852 26863196 MeRIP-seq:(Medium) rs1321166987 Functional Loss SNV dbSNP153 33..33 33 - - - 72998 RMVar_ID_72998 Human_SNP_ID_591224673 m1A Human chr16 + 2205813 2205812 2205813 TCCCCCCTGCCGGCTGCGGAGGTGGGGGGGGGACGGCGCCCCCGCCGTGTGCGTGGGGCGGGGAT TCCCCCCTGCCGGCTGCGGAGGTGGGGGGGGG_CGGCGCCCCCGCCGTGTGCGTGGGGCGGGGAT GA G MLST8 Ensembl:ENSG00000167965 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr16:2205767..2205875;chr16:2205768..2205869 26863196,32194978 MeRIP-seq:(Medium) rs551624542 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4356210 Human_Splice_Rec_1664933,Human_Splice_Rec_1665133,Human_Splice_Rec_1665147,Human_Splice_Rec_1665163 72999 RMVar_ID_72999 Human_SNP_ID_591224716 m1A Human chr16 - 2205877 2205877 2205877 GTAGGTTCAGGGACACGCGTCACACGCGTGATACCTGGCTCCGGGGCTCCAGGGCGCGTGCTCCA GTAGGTTCAGGGACACGCGTCACACGCGTGATCCCTGGCTCCGGGGCTCCAGGGCGCGTGCTCCA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2205776..2205900 26863410 MeRIP-seq:(Medium) rs1407663880 Functional Loss SNV dbSNP153 33..33 33 - - - 73000 RMVar_ID_73000 Human_SNP_ID_591224780 m1A Human chr16 - 2205986 2205986 2205986 ATGTGAAGTACTTAGAAGACACTCTCTGTGCTAAGTAGATTATAGACCCACAAGGCGCTGCCGAA ATGTGAAGTACTTAGAAGACACTCTCTGTGCTTAGTAGATTATAGACCCACAAGGCGCTGCCGAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2205973..2206150 26863196 MeRIP-seq:(Medium) rs952405705 Functional Loss SNV dbSNP153 33..33 33 - - - 73001 RMVar_ID_73001 Human_SNP_ID_591224843 m1A Human chr16 - 2206056 2206055 2206057 CATGGTGTGGCCTGCACGGGCCCTAGAGCTGAACGGCAGGGGTCAAAGGTCAGAGCATCTGCAGA CATGGTGTGGCCTGCACGGGCCCTAGAGCTG__CGGCAGGGGTCAAAGGTCAGAGCATCTGCAGA GTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2206033..2206147 26863196 MeRIP-seq:(Medium) rs1429110249 Functional Loss DEL dbSNP153 32..33 33 - - - 73002 RMVar_ID_73002 Human_SNP_ID_591224869 m1A Human chr16 + 2206100 2206100 2206100 GCCCGTGCAGGCCACACCATGAACACCTCCCCAGGCACGGTGGGCAGTGACCCGGTCATCCTGGC GCCCGTGCAGGCCACACCATGAACACCTCCCCGGGCACGGTGGGCAGTGACCCGGTCATCCTGGC A G MLST8 Ensembl:ENSG00000167965 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2206051..2206150 26863196 MeRIP-seq:(Medium) rs200101621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470501,Human_RBP_ID_1514218,Human_RBP_ID_4393499,Human_RBP_ID_18189829,Human_RBP_ID_26809866 Human_Splice_Rec_1664856,Human_Splice_Rec_1664864,Human_Splice_Rec_1664876,Human_Splice_Rec_1664892,Human_Splice_Rec_1664908,Human_Splice_Rec_1664920,Human_Splice_Rec_1664934,Human_Splice_Rec_1664940,Human_Splice_Rec_1664950,Human_Splice_Rec_1664960,Human_Splice_Rec_1664974,Human_Splice_Rec_1664988,Human_Splice_Rec_1665004,Human_Splice_Rec_1665010,Human_Splice_Rec_1665020,Human_Splice_Rec_1665030,Human_Splice_Rec_1665034,Human_Splice_Rec_1665058,Human_Splice_Rec_1665062,Human_Splice_Rec_1665074,Human_Splice_Rec_1665088,Human_Splice_Rec_1665094,Human_Splice_Rec_1665106,Human_Splice_Rec_1665120,Human_Splice_Rec_1665134,Human_Splice_Rec_1665148,Human_Splice_Rec_1665164 Clinvar_Rec_314,Clinvar_Rec_315 73003 RMVar_ID_73003 Human_SNP_ID_591224870 m1A Human chr16 + 2206100 2206100 2206100 GCCCGTGCAGGCCACACCATGAACACCTCCCCAGGCACGGTGGGCAGTGACCCGGTCATCCTGGC GCCCGTGCAGGCCACACCATGAACACCTCCCCTGGCACGGTGGGCAGTGACCCGGTCATCCTGGC A T MLST8 Ensembl:ENSG00000167965 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2206051..2206150 26863196 MeRIP-seq:(Medium) rs200101621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470501,Human_RBP_ID_1514218,Human_RBP_ID_4393499,Human_RBP_ID_18189829,Human_RBP_ID_26809866 Human_Splice_Rec_1664856,Human_Splice_Rec_1664864,Human_Splice_Rec_1664876,Human_Splice_Rec_1664892,Human_Splice_Rec_1664908,Human_Splice_Rec_1664920,Human_Splice_Rec_1664934,Human_Splice_Rec_1664940,Human_Splice_Rec_1664950,Human_Splice_Rec_1664960,Human_Splice_Rec_1664974,Human_Splice_Rec_1664988,Human_Splice_Rec_1665004,Human_Splice_Rec_1665010,Human_Splice_Rec_1665020,Human_Splice_Rec_1665030,Human_Splice_Rec_1665034,Human_Splice_Rec_1665058,Human_Splice_Rec_1665062,Human_Splice_Rec_1665074,Human_Splice_Rec_1665088,Human_Splice_Rec_1665094,Human_Splice_Rec_1665106,Human_Splice_Rec_1665120,Human_Splice_Rec_1665134,Human_Splice_Rec_1665148,Human_Splice_Rec_1665164 Clinvar_Rec_314,Clinvar_Rec_315 73004 RMVar_ID_73004 Human_SNP_ID_591224913 m1A Human chr16 + 2206188 2206188 2206188 TGCGCTTCTGGCAGGCCCACAGCGGCATCTGCACCCGGACGGTGCAGCACCAGGACTCCGTATCC TGCGCTTCTGGCAGGCCCACAGCGGCATCTGCCCCCGGACGGTGCAGCACCAGGACTCCGTATCC A C MLST8 Ensembl:ENSG00000167965 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2206176..2206225 26863196 MeRIP-seq:(Medium) rs1427362756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470502,Human_RBP_ID_4393500,Human_RBP_ID_26809866 Human_Splice_Rec_1664857,Human_Splice_Rec_1664865,Human_Splice_Rec_1664877,Human_Splice_Rec_1664893,Human_Splice_Rec_1664909,Human_Splice_Rec_1664921,Human_Splice_Rec_1664935,Human_Splice_Rec_1664941,Human_Splice_Rec_1664951,Human_Splice_Rec_1664961,Human_Splice_Rec_1664975,Human_Splice_Rec_1664989,Human_Splice_Rec_1665005,Human_Splice_Rec_1665011,Human_Splice_Rec_1665021,Human_Splice_Rec_1665031,Human_Splice_Rec_1665035,Human_Splice_Rec_1665043,Human_Splice_Rec_1665059,Human_Splice_Rec_1665063,Human_Splice_Rec_1665075,Human_Splice_Rec_1665089,Human_Splice_Rec_1665095,Human_Splice_Rec_1665107,Human_Splice_Rec_1665121,Human_Splice_Rec_1665135,Human_Splice_Rec_1665149,Human_Splice_Rec_1665165,Human_Splice_Rec_1665179 73005 RMVar_ID_73005 Human_SNP_ID_591225691 m1A Human chr16 - 2208026 2208026 2208026 ACCTGGGAAGCCTGGCCCCAAGCAAGGGCCACACCTGGCAAGCCAAGAACAGGAGGCCACGCCTG ACCTGGGAAGCCTGGCCCCAAGCAAGGGCCACGCCTGGCAAGCCAAGAACAGGAGGCCACGCCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2208024..2208124 32194978 MeRIP-seq:(Medium) rs1200391856 Functional Loss SNV dbSNP153 33..33 33 - - - 73006 RMVar_ID_73006 Human_SNP_ID_591226102 m1A Human chr16 + 2208744 2208744 2208744 CTTGGCCTGCACCTGCGCTCTTAGCCCTGCACAATCTCCCCCTCCAGCTTCCTCGGACAACCTGG CTTGGCCTGCACCTGCGCTCTTAGCCCTGCACCATCTCCCCCTCCAGCTTCCTCGGACAACCTGG A C MLST8 Ensembl:ENSG00000167965 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2208741..2208899 26863196 MeRIP-seq:(Medium) rs1301088570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470510 73007 RMVar_ID_73007 Human_SNP_ID_591228792 m1A Human chr16 - 2214287 2214287 2214287 CGGCGACTGGCTGCACGCGCCGCTGGAGCCCGACGTGCGCGCGGTGGTGGTGGGCTTTGACCCGC CGGCGACTGGCTGCACGCGCCGCTGGAGCCCGTCGTGCGCGCGGTGGTGGTGGGCTTTGACCCGC T A PGP Ensembl:ENSG00000184207 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2214201..2214425 26863410 MeRIP-seq:(Medium) rs1348620168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4397168,Human_RBP_ID_8429708,Human_RBP_ID_22052782 73008 RMVar_ID_73008 Human_SNP_ID_591228981 m1A Human chr16 - 2214752 2214752 2214752 GGCGGCGATGGCGGCGGCGGAGGCCGGTGGCGACGACGCCCGCTGCGTGCGGCTGAGCGCCGAGC GGCGGCGATGGCGGCGGCGGAGGCCGGTGGCGGCGACGCCCGCTGCGTGCGGCTGAGCGCCGAGC T C PGP Ensembl:ENSG00000184207 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2214138..2214825 26863196 MeRIP-seq:(Medium) rs1252144033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235182,Human_RBP_ID_763217,Human_RBP_ID_4356350,Human_RBP_ID_17669659,Human_RBP_ID_18418892,Human_RBP_ID_26757136 73009 RMVar_ID_73009 Human_SNP_ID_591228989 m1A Human chr16 - 2214764 2214764 2214764 CGGCGGCCGGCGGGCGGCGATGGCGGCGGCGGAGGCCGGTGGCGACGACGCCCGCTGCGTGCGGC CGGCGGCCGGCGGGCGGCGATGGCGGCGGCGGGGGCCGGTGGCGACGACGCCCGCTGCGTGCGGC T C PGP Ensembl:ENSG00000184207 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2214655..2214825 26863196 MeRIP-seq:(Medium) rs1344237746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235182,Human_RBP_ID_763217,Human_RBP_ID_4392777,Human_RBP_ID_17669659,Human_RBP_ID_18418892,Human_RBP_ID_26757136 73010 RMVar_ID_73010 Human_SNP_ID_591228990 m1A Human chr16 - 2214764 2214764 2214764 CGGCGGCCGGCGGGCGGCGATGGCGGCGGCGGAGGCCGGTGGCGACGACGCCCGCTGCGTGCGGC CGGCGGCCGGCGGGCGGCGATGGCGGCGGCGGCGGCCGGTGGCGACGACGCCCGCTGCGTGCGGC T G PGP Ensembl:ENSG00000184207 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2214655..2214825 26863196 MeRIP-seq:(Medium) rs1344237746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235182,Human_RBP_ID_763217,Human_RBP_ID_4392777,Human_RBP_ID_17669659,Human_RBP_ID_18418892,Human_RBP_ID_26757136 73011 RMVar_ID_73011 Human_SNP_ID_591232203 m1A Human chr16 + 2223684 2223684 2223684 TACGGCAGAAGCCCAGGCCGAAGCCGGGCGGGAAGCGGGCGAGGGTGCAGTTGCGGCGGTGGCGG TACGGCAGAAGCCCAGGCCGAAGCCGGGCGGGGAGCGGGCGAGGGTGCAGTTGCGGCGGTGGCGG A G E4F1 Ensembl:ENSG00000167967 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2223641..2223761 26863196 MeRIP-seq:(Medium) rs758540723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393504,Human_RBP_ID_18418641 Human_Splice_Rec_1665235,Human_Splice_Rec_1665255,Human_Splice_Rec_1665281,Human_Splice_Rec_1665307 73012 RMVar_ID_73012 Human_SNP_ID_591232245 m1A Human chr16 - 2223758 2223758 2223758 CTCCGGGTCGGCCCGGTTACCTTCCTCGCTGAAGGGCGCCGGGAGGCCGAGGAAGCCGCTGGGGG CTCCGGGTCGGCCCGGTTACCTTCCTCGCTGACGGGCGCCGGGAGGCCGAGGAAGCCGCTGGGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2223664..2223814 32194978 MeRIP-seq:(Medium) rs915172633 Functional Loss SNV dbSNP153 33..33 33 - - - 73013 RMVar_ID_73013 Human_SNP_ID_591232246 m1A Human chr16 + 2223765 2223765 2223765 CGGCTTCCTCGGCCTCCCGGCGCCCTTCAGCGAGGAAGGTAACCGGGCCGACCCGGAGGGTGCGG CGGCTTCCTCGGCCTCCCGGCGCCCTTCAGCGGGGAAGGTAACCGGGCCGACCCGGAGGGTGCGG A G E4F1 Ensembl:ENSG00000167967 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2223679..2223765 26863410 MeRIP-seq:(Medium) rs760318402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393504,Human_RBP_ID_18418641,Human_RBP_ID_19072999 Human_Splice_Rec_1665235,Human_Splice_Rec_1665255,Human_Splice_Rec_1665281,Human_Splice_Rec_1665307 73014 RMVar_ID_73014 Human_SNP_ID_591234257 m1A Human chr16 - 2229945 2229945 2229945 GGGAAGATTCTGGGAGGGACACGGCAGAGACCACCCGGGAAAGCTGACGGGAGAGAGCACAGCCC GGGAAGATTCTGGGAGGGACACGGCAGAGACCTCCCGGGAAAGCTGACGGGAGAGAGCACAGCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2229939..2230026 26863196 MeRIP-seq:(Medium) rs186472853 Functional Loss SNV dbSNP153 33..33 33 - - - 73015 RMVar_ID_73015 Human_SNP_ID_591234964 m1A Human chr16 + 2232318 2232318 2232318 TGAGCAGGCCCAGGTGAAGCTACTGGTGAACAAGGATGGCCGCTATGTGTGTGCGCTGTGCCACA TGAGCAGGCCCAGGTGAAGCTACTGGTGAACAGGGATGGCCGCTATGTGTGTGCGCTGTGCCACA A G E4F1 Ensembl:ENSG00000167967 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2232166..2232362;chr16:2232153..2232358 26863196 MeRIP-seq:(Medium) rs779615574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888327,Human_RBP_ID_3947155,Human_RBP_ID_5355542,Human_RBP_ID_18983048,Human_RBP_ID_26328488 Human_Splice_Rec_1665241,Human_Splice_Rec_1665261,Human_Splice_Rec_1665287,Human_Splice_Rec_1665313,Human_Splice_Rec_1665323,Human_Splice_Rec_1665329 RMVar_hsa_circ_341681 73016 RMVar_ID_73016 Human_SNP_ID_591235328 m1A Human chr16 + 2233163 2233163 2233163 TCCACGTCCAGATGCAGGAGCTGTCCCTGGGCATGAAAGCCCTGGCCCCAGAGGTGGGGGCGACG TCCACGTCCAGATGCAGGAGCTGTCCCTGGGCGTGAAAGCCCTGGCCCCAGAGGTGGGGGCGACG A G E4F1 Ensembl:ENSG00000167967 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2233012..2233211 32194978 MeRIP-seq:(Medium) rs186588193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46294,Human_RBP_ID_235032,Human_RBP_ID_9372086,Human_RBP_ID_18985225,Human_RBP_ID_22473739 Human_Splice_Rec_1665247,Human_Splice_Rec_1665267,Human_Splice_Rec_1665293 RMVar_hsa_circ_14696,RMVar_hsa_circ_341681 73017 RMVar_ID_73017 Human_SNP_ID_591235798 m1A Human chr16 - 2234303 2234303 2234303 AGTGGACGCGCCGGTGGCCACGCACATGGGCAATGGTCTTGTAGAGCTTCCCGCAGTCGCCACAG AGTGGACGCGCCGGTGGCCACGCACATGGGCAGTGGTCTTGTAGAGCTTCCCGCAGTCGCCACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2234252..2234353 32194978 MeRIP-seq:(Medium) rs747632415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1514295,Human_RBP_ID_18675053 73018 RMVar_ID_73018 Human_SNP_ID_591236310 m1A Human chr16 + 2235326 2235326 2235326 GTCACCATGGACGAGGAGACGGCGCTGGGCCCAGAGGCGGCTGCCGCCGACACCATCACCATCGC GTCACCATGGACGAGGAGACGGCGCTGGGCCCTGAGGCGGCTGCCGCCGACACCATCACCATCGC A T E4F1 Ensembl:ENSG00000167967 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2235276..2235403 26863196 MeRIP-seq:(Medium) rs1408611024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947160,Human_RBP_ID_9372087,Human_RBP_ID_26809876,Human_RBP_ID_26940413,Human_RBP_ID_27811488 73019 RMVar_ID_73019 Human_SNP_ID_591239283 m1A Human chr16 + 2242758 2242758 2242758 AGCGAGGCGCCCACAAGCCCAGGGAGGCCTGGAGCCAGCAGAAGTGGGCGGGGCAGGAAGGAGCC AGCGAGGCGCCCACAAGCCCAGGGAGGCCTGGGGCCAGCAGAAGTGGGCGGGGCAGGAAGGAGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2242757..2242858 32194978 MeRIP-seq:(Medium) rs1198027993 Functional Loss SNV dbSNP153 33..33 33 - - - 73020 RMVar_ID_73020 Human_SNP_ID_591242412 m1A Human chr16 + 2251420 2251407 2251420 CCCGCTCCGTCCGCCCGAGGGCCGCGCCCGGGAGCCGGGCCCCTGCGAAGGCAGCGTGGGGGAGC CCCGCTCCGTCCGCCCGAGG_____________GCCGGGCCCCTGCGAAGGCAGCGTGGGGGAGC GGCCGCGCCCGGGA G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:2251334..2251538 26863410 MeRIP-seq:(Medium) rs1416484831 Functional Loss DEL dbSNP153 21..33 33 - - - 73021 RMVar_ID_73021 Human_SNP_ID_591242483 m1A Human chr16 + 2251526 2251526 2251526 TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCAGAACGCGCGCCGGGACTCGCACAGAAGCCACC TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCCGAACGCGCGCCGGGACTCGCACAGAAGCCACC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2251301..2251575 26863196 MeRIP-seq:(Medium) rs199944223 Functional Loss SNV dbSNP153 33..33 33 - - - 73022 RMVar_ID_73022 Human_SNP_ID_591242484 m1A Human chr16 + 2251526 2251526 2251526 TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCAGAACGCGCGCCGGGACTCGCACAGAAGCCACC TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCGGAACGCGCGCCGGGACTCGCACAGAAGCCACC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2251301..2251575 26863196 MeRIP-seq:(Medium) rs199944223 Functional Loss SNV dbSNP153 33..33 33 - - - 73023 RMVar_ID_73023 Human_SNP_ID_591242485 m1A Human chr16 + 2251526 2251526 2251526 TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCAGAACGCGCGCCGGGACTCGCACAGAAGCCACC TGCCCACCCCGGGTTTCGCACCCGCGCGGAGCTGAACGCGCGCCGGGACTCGCACAGAAGCCACC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2251301..2251575 26863196 MeRIP-seq:(Medium) rs199944223 Functional Loss SNV dbSNP153 33..33 33 - - - 73024 RMVar_ID_73024 Human_SNP_ID_591242487 m1A Human chr16 + 2251529 2251529 2251529 CCACCCCGGGTTTCGCACCCGCGCGGAGCAGAACGCGCGCCGGGACTCGCACAGAAGCCACCAGC CCACCCCGGGTTTCGCACCCGCGCGGAGCAGAGCGCGCGCCGGGACTCGCACAGAAGCCACCAGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2246851..2251600 26863196 MeRIP-seq:(Medium) rs1189628478 Functional Loss SNV dbSNP153 33..33 33 - - - 73025 RMVar_ID_73025 Human_SNP_ID_591243301 m1A Human chr16 + 2253731 2253731 2253731 TCTGCCACTGAACTGACTCTTAGAAACCGGAAACGGATGAGCTTTCTAGCCAGAAAACCGGAGGG TCTGCCACTGAACTGACTCTTAGAAACCGGAAGCGGATGAGCTTTCTAGCCAGAAAACCGGAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2253683..2253812 26863196 MeRIP-seq:(Medium) rs982787528 Functional Loss SNV dbSNP153 33..33 33 - - - 73026 RMVar_ID_73026 Human_SNP_ID_591243433 m1A Human chr16 - 2253963 2253962 2253963 GGAGCCGCTCCAGCTCCAACTCCTCCCGATAAACAGGCCACTGAAGCTCTCGCCCCTGTAACTTA GGAGCCGCTCCAGCTCCAACTCCTCCCGATAA_CAGGCCACTGAAGCTCTCGCCCCTGTAACTTA GT G RNPS1 Ensembl:ENSG00000205937 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2253901..2254075;chr16:2253876..2254025 31548705,26863196 m1A-IP-seq:(High) rs1490417004 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_470622,Human_RBP_ID_1003458,Human_RBP_ID_1281337,Human_RBP_ID_4397224,Human_RBP_ID_12690817,Human_RBP_ID_17253351,Human_RBP_ID_17369042,Human_RBP_ID_17485495,Human_RBP_ID_18284756,Human_RBP_ID_21888712,Human_RBP_ID_22440826,Human_RBP_ID_27440100 RMVar_hsa_circ_377688,RMVar_hsa_circ_175728 73027 RMVar_ID_73027 Human_SNP_ID_591246964 m1A Human chr16 + 2264583 2264583 2264583 AAAAATCTTACAGAAGGATTACCTAGTGCTGGACTTTTTATTATTTTCTTTGACTCCTAGCAAGC AAAAATCTTACAGAAGGATTACCTAGTGCTGGGCTTTTTATTATTTTCTTTGACTCCTAGCAAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2264576..2264650 26863196 MeRIP-seq:(Medium) rs1417508218 Functional Loss SNV dbSNP153 33..33 33 - - - 73028 RMVar_ID_73028 Human_SNP_ID_591247025 m1A Human chr16 + 2264758 2264758 2264758 TCCCTAATCGATTGCAATTTACGCCAAAGAGCAGCCTAATAACAAGATAAAAGGGTTTAAAGAGT TCCCTAATCGATTGCAATTTACGCCAAAGAGCGGCCTAATAACAAGATAAAAGGGTTTAAAGAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:2264701..2264775;chr16:2264246..2264787;chr16:2264147..2264787 26863196 MeRIP-seq:(Medium) rs1337739058 Functional Loss SNV dbSNP153 33..33 33 - - - 73029 RMVar_ID_73029 Human_SNP_ID_591247882 m1A Human chr16 + 2267557 2267557 2267557 TCGCGGAGTACACGTTTGAATTAATGACTCCGAAGGGGGGATCGGCCGACCTTCCACCGCATCCC TCGCGGAGTACACGTTTGAATTAATGACTCCGTAGGGGGGATCGGCCGACCTTCCACCGCATCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2267555..2268125 26863196 MeRIP-seq:(Medium) rs1209363767 Functional Loss SNV dbSNP153 33..33 33 - - - 73030 RMVar_ID_73030 Human_SNP_ID_591248047 m1A Human chr16 + 2267907 2267905 2267907 CTCGACACCTCCCACTCCGCCCGCCCCGGGCCACACTCTTTCTTCTCGGAGCCCGCACCGCGCTG CTCGACACCTCCCACTCCGCCCGCCCCGGGC__CACTCTTTCTTCTCGGAGCCCGCACCGCGCTG CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2267904..2268125 26863196 MeRIP-seq:(Medium) rs1567331340 Functional Loss DEL dbSNP153 32..33 33 - - - 73031 RMVar_ID_73031 Human_SNP_ID_591248086 m1A Human chr16 - 2268004 2268004 2268004 CGACTGCATCCGTGTTTCGGGGGCTGCCCGGCAGGCCCGGCAGGACGCCTCGTGAAGCCGGTCCA CGACTGCATCCGTGTTTCGGGGGCTGCCCGGCGGGCCCGGCAGGACGCCTCGTGAAGCCGGTCCA T C RNPS1 Ensembl:ENSG00000205937 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2267981..2268075 26863410 MeRIP-seq:(Medium) rs894788786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235246,Human_RBP_ID_4356740,Human_RBP_ID_5113321,Human_RBP_ID_5357447,Human_RBP_ID_19070649,Human_RBP_ID_22052792,Human_RBP_ID_22356677 Human_Splice_Rec_1665531,Human_Splice_Rec_1665607 73032 RMVar_ID_73032 Human_SNP_ID_591248087 m1A Human chr16 - 2268004 2268004 2268004 CGACTGCATCCGTGTTTCGGGGGCTGCCCGGCAGGCCCGGCAGGACGCCTCGTGAAGCCGGTCCA CGACTGCATCCGTGTTTCGGGGGCTGCCCGGCCGGCCCGGCAGGACGCCTCGTGAAGCCGGTCCA T G RNPS1 Ensembl:ENSG00000205937 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2267981..2268075 26863410 MeRIP-seq:(Medium) rs894788786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235246,Human_RBP_ID_4356740,Human_RBP_ID_5113321,Human_RBP_ID_5357447,Human_RBP_ID_19070649,Human_RBP_ID_22052792,Human_RBP_ID_22356677 Human_Splice_Rec_1665531,Human_Splice_Rec_1665607 73033 RMVar_ID_73033 Human_SNP_ID_591248410 m1A Human chr16 - 2268635 2268635 2268635 GCCGCGTCCACGGGAACACCCCAAACGCCACCAGTGGATTTTGACCGCACGAACGCACGCCCTGC GCCGCGTCCACGGGAACACCCCAAACGCCACCCGTGGATTTTGACCGCACGAACGCACGCCCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2268252..2271736 26863196 MeRIP-seq:(Medium) rs1567332120 Functional Loss SNV dbSNP153 33..33 33 - - - 73034 RMVar_ID_73034 Human_SNP_ID_591258015 m1A Human chr16 - 2299526 2299526 2299526 CAGGGCAGCCTCTGCCTTTCCTGCAGGTGTTCAGGGTGGGAAATAAGGACAGGGCGGCCGTCAGA CAGGGCAGCCTCTGCCTTTCCTGCAGGTGTTCGGGGTGGGAAATAAGGACAGGGCGGCCGTCAGA T C ABCA3 Ensembl:ENSG00000167972 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2299503..2300076 26863196 MeRIP-seq:(Medium) rs905822370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629,Human_RBP_ID_888339 Human_Splice_Rec_1665728,Human_Splice_Rec_1665790,Human_Splice_Rec_1665864 RMVar_hsa_circ_12861,RMVar_hsa_circ_15644 73035 RMVar_ID_73035 Human_SNP_ID_591261129 m1A Human chr16 - 2308613 2308613 2308613 CCGGGTCTTCCAACACCTGCAGCCAACATGGCAGCAGCCTTCGGAGGCTTCCTCTACTTCTTCAC CCGGGTCTTCCAACACCTGCAGCCAACATGGCCGCAGCCTTCGGAGGCTTCCTCTACTTCTTCAC T G ABCA3 Ensembl:ENSG00000167972 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2308556..2308669 26863196 MeRIP-seq:(Medium) rs907704011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1665722,Human_Splice_Rec_1665858 RMVar_hsa_circ_673,RMVar_hsa_circ_12861,RMVar_hsa_circ_122369,RMVar_hsa_circ_21275,RMVar_hsa_circ_175738 73036 RMVar_ID_73036 Human_SNP_ID_591271468 m1A Human chr16 + 2341578 2341578 2341578 AGGGTCGGGTTCACCTGAGGGGAGGGTCGGGGAGGGTCCGGAGAGGGTCGGGGTCACCTGAGGAG AGGGTCGGGTTCACCTGAGGGGAGGGTCGGGGGGGGTCCGGAGAGGGTCGGGGTCACCTGAGGAG A G ABCA17P Ensembl:ENSG00000238098 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2341570..2341909 26863196 MeRIP-seq:(Medium) rs1255746948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510659 73037 RMVar_ID_73037 Human_SNP_ID_591294339 m1A Human chr16 + 2429482 2429482 2429482 CGGGCTCCGGCGGCAGCGACGCGAGCGCGGCGATGGGGAGCGGCGGCGGTGAGTGCGGGGCGATG CGGGCTCCGGCGGCAGCGACGCGAGCGCGGCGGTGGGGAGCGGCGGCGGTGAGTGCGGGGCGATG A G CCNF Ensembl:ENSG00000162063 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2429436..2429549 26863196 MeRIP-seq:(Medium) rs912796548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233953,Human_RBP_ID_4393513 Human_Splice_Rec_1665969,Human_Splice_Rec_1665999,Human_Splice_Rec_1666031 RMVar_hsa_circ_110860,RMVar_hsa_circ_175752 73038 RMVar_ID_73038 Human_SNP_ID_591294343 m1A Human chr16 + 2429488 2429488 2429488 CCGGCGGCAGCGACGCGAGCGCGGCGATGGGGAGCGGCGGCGGTGAGTGCGGGGCGATGTCCGCT CCGGCGGCAGCGACGCGAGCGCGGCGATGGGGGGCGGCGGCGGTGAGTGCGGGGCGATGTCCGCT A G CCNF Ensembl:ENSG00000162063 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2429447..2429574 26863196 MeRIP-seq:(Medium) rs944306963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233953,Human_RBP_ID_4393513 Human_Splice_Rec_1665969,Human_Splice_Rec_1665999,Human_Splice_Rec_1666031 RMVar_hsa_circ_110860,RMVar_hsa_circ_175752 73039 RMVar_ID_73039 Human_SNP_ID_591303102 m1A Human chr16 - 2455478 2455478 2455478 AGTCCAGGCTCCAGTCGAGGAAGCTGCCCAGCAGCGTCTCCTCCTGGCTGGACAGCTCCGCAGTG AGTCCAGGCTCCAGTCGAGGAAGCTGCCCAGCGGCGTCTCCTCCTGGCTGGACAGCTCCGCAGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2455427..2455507 26863196 MeRIP-seq:(Medium) rs201114363 Functional Loss SNV dbSNP153 33..33 33 - - - 73040 RMVar_ID_73040 Human_SNP_ID_591303595 m1A Human chr16 + 2456956 2456956 2456956 CCCGGAGAGCAGTGTTCCCCAGCAACAGGTGAAGCGGATAAACCTATGCATACACAGTGAGGAGG CCCGGAGAGCAGTGTTCCCCAGCAACAGGTGAGGCGGATAAACCTATGCATACACAGTGAGGAGG A G CCNF Ensembl:ENSG00000162063 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2456909..2457099 26863196 MeRIP-seq:(Medium) rs768080881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2093493 RMVar_hsa_circ_107076,RMVar_hsa_circ_127733,RMVar_hsa_circ_175754,RMVar_hsa_circ_105577,RMVar_hsa_circ_175756,RMVar_hsa_circ_124682,RMVar_hsa_circ_175757,RMVar_hsa_circ_175758,RMVar_hsa_circ_114364,RMVar_hsa_circ_84544,RMVar_hsa_circ_175759,RMVar_hsa_circ_175765,RMVar_hsa_circ_95904,RMVar_hsa_circ_175769,RMVar_hsa_circ_123818,RMVar_hsa_circ_126663,RMVar_hsa_circ_175770,RMVar_hsa_circ_175771,RMVar_hsa_circ_104844,RMVar_hsa_circ_121252,RMVar_hsa_circ_175775,RMVar_hsa_circ_175776 73041 RMVar_ID_73041 Human_SNP_ID_591304568 m1A Human chr16 - 2460172 2460172 2460172 ATCCTCCCACCCCCTCCTGCCGCGCAGGCCTCACCGGCGCGAGCAGCCCGCCGGCAGCATGAAGG ATCCTCCCACCCCCTCCTGCCGCGCAGGCCTCGCCGGCGCGAGCAGCCCGCCGGCAGCATGAAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2460154..2460315 26863196 MeRIP-seq:(Medium) rs1490058723 Functional Loss SNV dbSNP153 33..33 33 - - - 73042 RMVar_ID_73042 Human_SNP_ID_591304659 m1A Human chr16 - 2460338 2460338 2460338 CAGCCGACGGCAAACGCGCAGGCTCTGCTCCAATTGCAATTGTCGCTGTGCGCAGGCGTCCAGGG CAGCCGACGGCAAACGCGCAGGCTCTGCTCCATTTGCAATTGTCGCTGTGCGCAGGCGTCCAGGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2460126..2460424 26863410 MeRIP-seq:(Medium) rs1469120168 Functional Loss SNV dbSNP153 33..33 33 - - - 73043 RMVar_ID_73043 Human_SNP_ID_591304660 m1A Human chr16 - 2460338 2460338 2460338 CAGCCGACGGCAAACGCGCAGGCTCTGCTCCAATTGCAATTGTCGCTGTGCGCAGGCGTCCAGGG CAGCCGACGGCAAACGCGCAGGCTCTGCTCCAGTTGCAATTGTCGCTGTGCGCAGGCGTCCAGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2460126..2460424 26863410 MeRIP-seq:(Medium) rs1469120168 Functional Loss SNV dbSNP153 33..33 33 - - - 73044 RMVar_ID_73044 Human_SNP_ID_591304971 m1A Human chr16 + 2461014 2461014 2461014 CCCACCGCATTCCCCAGGCCAAGCTGGTGGCCATGCTTCAGACACGAGACCCACCAAGGGCCTCC CCCACCGCATTCCCCAGGCCAAGCTGGTGGCCGTGCTTCAGACACGAGACCCACCAAGGGCCTCC A G TEDC2 Ensembl:ENSG00000162062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2460964..2461046 26863196 MeRIP-seq:(Medium) rs536417775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5495327,Human_RBP_ID_22198815 73045 RMVar_ID_73045 Human_SNP_ID_591305533 m1A Human chr16 - 2462500 2462500 2462500 ACTGACCTGCCGAGAGCTCCTCCCTCATGCGCAGTCTCAGCAGCGAGCAGGCCTTCCGCAGGCGC ACTGACCTGCCGAGAGCTCCTCCCTCATGCGCGGTCTCAGCAGCGAGCAGGCCTTCCGCAGGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2462452..2462524 26863196 MeRIP-seq:(Medium) rs1164204623 Functional Loss SNV dbSNP153 33..33 33 - - - 73046 RMVar_ID_73046 Human_SNP_ID_591307773 m1A Human chr16 - 2468541 2468540 2468542 GCTCCGAAGGCAGACAGCCCAGGAGCAGACACAGCGCCGGCTCCCAACGGCGGGTGGTGTGGCCG GCTCCGAAGGCAGACAGCCCAGGAGCAGACA__GCGCCGGCTCCCAACGGCGGGTGGTGTGGCCG CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2468491..2468664 26863196 MeRIP-seq:(Medium) rs1209380176 Functional Loss DEL dbSNP153 32..33 33 - - - 73047 RMVar_ID_73047 Human_SNP_ID_591309601 m1A Human chr16 + 2473648 2473648 2473648 ATCCTCATCCCTCAGGTCCTCCACGGGCAGCGACCCCGCCCCTTCAGCCCCCACTGCCCTCCTGG ATCCTCATCCCTCAGGTCCTCCACGGGCAGCGGCCCCGCCCCTTCAGCCCCCACTGCCCTCCTGG A G NTN3 Ensembl:ENSG00000162068 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2473433..2473734 26863196 MeRIP-seq:(Medium) rs1198310978 Functional Loss SNV dbSNP153 33..33 33 - - - 73048 RMVar_ID_73048 Human_SNP_ID_591309764 m1A Human chr16 + 2474046 2474046 2474046 GAAGCCTCGTGCTACCCTGGAGGGACGCGTGGACGCGGCGCCTGCGGAGGCTGCAGCGACGCGAA GAAGCCTCGTGCTACCCTGGAGGGACGCGTGGGCGCGGCGCCTGCGGAGGCTGCAGCGACGCGAA A G NTN3 Ensembl:ENSG00000162068 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2474003..2474073 26863196 MeRIP-seq:(Medium) rs1331462586 Functional Loss SNV dbSNP153 33..33 33 - - - 73049 RMVar_ID_73049 Human_SNP_ID_591309984 m1A Human chr16 - 2474757 2474757 2474757 AGGGCTGGAAGGAGGTTCTGGGACGGGCCCTGAGCTGAGGAGCTGTGGCGCCGAGGGTCAGAGAC AGGGCTGGAAGGAGGTTCTGGGACGGGCCCTGGGCTGAGGAGCTGTGGCGCCGAGGGTCAGAGAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2474735..2474929 26863196 MeRIP-seq:(Medium) rs1192494921 Functional Loss SNV dbSNP153 33..33 33 - - - 73050 RMVar_ID_73050 Human_SNP_ID_591317150 m1A Human chr16 + 2500340 2500340 2500340 AGCACCCCGAGCTGACCAAGCCCCCACCCTTGATGGCTGCCGAGCCCACCGCCCCACTCAGCCAC AGCACCCCGAGCTGACCAAGCCCCCACCCTTGTTGGCTGCCGAGCCCACCGCCCCACTCAGCCAC A T AC093525.2,TBC1D24 Ensembl:ENSG00000260272,Ensembl:ENSG00000162065 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2500289..2500394 26863196 MeRIP-seq:(Medium) rs1437087933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1666212,Human_Splice_Rec_1666226,Human_Splice_Rec_1666238,Human_Splice_Rec_1666254,Human_Splice_Rec_1666268,Human_Splice_Rec_1666278,Human_Splice_Rec_1666288,Human_Splice_Rec_1666294 Human_miRNA_ID_2873754,Human_miRNA_ID_2981717 RMVar_hsa_circ_110319,RMVar_hsa_circ_265739,RMVar_hsa_circ_175779 73051 RMVar_ID_73051 Human_SNP_ID_591317398 m1A Human chr16 - 2500905 2500905 2500905 GAAGCCCCAGGCCTCCACGGCAGCAATGAGGAAGTTCTCGGAGCAGAGGGGCTGGTTGTTGAAGG GAAGCCCCAGGCCTCCACGGCAGCAATGAGGAGGTTCTCGGAGCAGAGGGGCTGGTTGTTGAAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2500806..2500956 32194978 MeRIP-seq:(Medium) rs1060502502 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_316 73052 RMVar_ID_73052 Human_SNP_ID_591317527 m1A Human chr16 + 2501303 2501285 2501304 CTGGGTCTTGCTGCCCCTGAGCCTCTCTAGGCAGCCTGAGCCCCTGGGGTGGGAGTACAACGGCA CTGGGTCTTGCTGCC___________________CCTGAGCCCCTGGGGTGGGAGTACAACGGCA CCCTGAGCCTCTCTAGGCAG C AC093525.2,TBC1D24 Ensembl:ENSG00000260272,Ensembl:ENSG00000162065 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2501254..2501504 32194978 MeRIP-seq:(Medium) rs1332894146 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_3508829,Human_RBP_ID_8186792,Human_RBP_ID_18458329 RMVar_hsa_circ_95560,RMVar_hsa_circ_110319,RMVar_hsa_circ_265739,RMVar_hsa_circ_175779,RMVar_hsa_circ_175780 73053 RMVar_ID_73053 Human_SNP_ID_591317972 m1A Human chr16 - 2502990 2502990 2502990 CTCCTGGAGGGCTCCCTCTGGAAGAGGCTTGCAGCATTCCAGTCATAGAATGTGGGTGAGCACTA CTCCTGGAGGGCTCCCTCTGGAAGAGGCTTGCCGCATTCCAGTCATAGAATGTGGGTGAGCACTA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2502896..2502997 32194978 MeRIP-seq:(Medium) rs182867476 Functional Loss SNV dbSNP153 33..33 33 - - - 73054 RMVar_ID_73054 Human_SNP_ID_591318241 m1A Human chr16 + 2503868 2503865 2503868 AGGCGTGAGCCACCGCGCCTAGCCTATTTTTTAATTTTTTTGAATAGACCACTTTGTGCTGAATA AGGCGTGAGCCACCGCGCCTAGCCTATTTT___ATTTTTTTGAATAGACCACTTTGTGCTGAATA TTTA T AC093525.2,TBC1D24 Ensembl:ENSG00000260272,Ensembl:ENSG00000162065 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1239330118 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_12703820 RMVar_hsa_circ_95560,RMVar_hsa_circ_110319,RMVar_hsa_circ_265739,RMVar_hsa_circ_175779,RMVar_hsa_circ_175780 73055 RMVar_ID_73055 Human_SNP_ID_591318243 m1A Human chr16 + 2503868 2503868 2503868 AGGCGTGAGCCACCGCGCCTAGCCTATTTTTTAATTTTTTTGAATAGACCACTTTGTGCTGAATA AGGCGTGAGCCACCGCGCCTAGCCTATTTTTTTATTTTTTTGAATAGACCACTTTGTGCTGAATA A T AC093525.2,TBC1D24 Ensembl:ENSG00000260272,Ensembl:ENSG00000162065 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4786287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12703820 Clinvar_Rec_317 RMVar_hsa_circ_95560,RMVar_hsa_circ_110319,RMVar_hsa_circ_265739,RMVar_hsa_circ_175779,RMVar_hsa_circ_175780 73056 RMVar_ID_73056 Human_SNP_ID_591321030 m1A Human chr16 + 2513785 2513785 2513785 CGGCGCCCGGAAACACCCGCGGAGGCCGAGGCAGGGCGGGGCCGGGCGCCGGGGCCGGGTCGCTG CGGCGCCCGGAAACACCCGCGGAGGCCGAGGCGGGGCGGGGCCGGGCGCCGGGGCCGGGTCGCTG A G AC093525.2 Ensembl:ENSG00000260272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2513735..2513919 26863196 MeRIP-seq:(Medium) rs560187647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4358903 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779 73057 RMVar_ID_73057 Human_SNP_ID_591321158 m1A Human chr16 + 2514021 2514021 2514021 GGGCCGGATCGCCTTCGCCGCCGCCCGCCCGCAAACCTTCGTGCCCGGCCCGTCCTCGCCCCCGC GGGCCGGATCGCCTTCGCCGCCGCCCGCCCGCCAACCTTCGTGCCCGGCCCGTCCTCGCCCCCGC A C AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding intron,5'UTR,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2513951..2514150 26863196 MeRIP-seq:(Medium) rs973580366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45680,Human_RBP_ID_471300,Human_RBP_ID_4358909,Human_RBP_ID_5440284,Human_RBP_ID_5464835,Human_RBP_ID_5495334,Human_RBP_ID_9324872,Human_RBP_ID_17371239,Human_RBP_ID_22532653,Human_RBP_ID_26446660,Human_RBP_ID_26941156,Human_RBP_ID_27239357 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779 73058 RMVar_ID_73058 Human_SNP_ID_591321168 m1A Human chr16 - 2514030 2514030 2514030 GTGGCGGAGGCGGGGGCGAGGACGGGCCGGGCACGAAGGTTTGCGGGCGGGCGGCGGCGAAGGCG GTGGCGGAGGCGGGGGCGAGGACGGGCCGGGCTCGAAGGTTTGCGGGCGGGCGGCGGCGAAGGCG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2513951..2514251 26863196 MeRIP-seq:(Medium) rs911564328 Functional Loss SNV dbSNP153 33..33 33 - - - 73059 RMVar_ID_73059 Human_SNP_ID_591321192 m1A Human chr16 + 2514061 2514049 2514061 GTGCCCGGCCCGTCCTCGCCCCCGCCTCCGCCACCGCCTCGGCCCGCAGAGCTTGCCCCCTCCCC GTGCCCGGCCCGTCCTCGCCC____________CCGCCTCGGCCCGCAGAGCTTGCCCCCTCCCC CCCGCCTCCGCCA C AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding intron,5'UTR,5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:2513951..2514150 26863410 MeRIP-seq:(Medium) rs1283282970 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_45680,Human_RBP_ID_234237,Human_RBP_ID_482736,Human_RBP_ID_762089,Human_RBP_ID_894633,Human_RBP_ID_4358910,Human_RBP_ID_8430665,Human_RBP_ID_9324872,Human_RBP_ID_17371240,Human_RBP_ID_18676017,Human_RBP_ID_18939907,Human_RBP_ID_22532752 Human_Splice_Rec_1666307 Human_miRNA_ID_2395824 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779 73060 RMVar_ID_73060 Human_SNP_ID_591321217 m1A Human chr16 - 2514082 2514082 2514082 GACTCGGACATGTCTGCGGGTGGGGAGGGGGCAAGCTCTGCGGGCCGAGGCGGTGGCGGAGGCGG GACTCGGACATGTCTGCGGGTGGGGAGGGGGCCAGCTCTGCGGGCCGAGGCGGTGGCGGAGGCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr16:2513951..2514217;chr16:2513951..2514150 26863196 MeRIP-seq:(Medium) rs779508114 Functional Loss SNV dbSNP153 33..33 33 - - - 73061 RMVar_ID_73061 Human_SNP_ID_591321240 m1A Human chr16 + 2514111 2514111 2514111 GCTTGCCCCCTCCCCACCCGCAGACATGTCCGAGTCCAAGAGCGGCCCCGAGTATGCTTCGTTTT GCTTGCCCCCTCCCCACCCGCAGACATGTCCGGGTCCAAGAGCGGCCCCGAGTATGCTTCGTTTT A G AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2513951..2514239 26863196 MeRIP-seq:(Medium) rs1272783067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45680,Human_RBP_ID_471303,Human_RBP_ID_1515243,Human_RBP_ID_4393519,Human_RBP_ID_9324872,Human_RBP_ID_12703883,Human_RBP_ID_17371241,Human_RBP_ID_18939908,Human_RBP_ID_22473745,Human_RBP_ID_23684542,Human_RBP_ID_26440246,Human_RBP_ID_26941157 Human_Splice_Rec_1666303,Human_Splice_Rec_1666307,Human_Splice_Rec_1666317 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779 73062 RMVar_ID_73062 Human_SNP_ID_591323014 m1A Human chr16 + 2519268 2519268 2519268 GCACAGCCAAGAGCGGTACCGGCATTGCGGCCATGTCTGTCATGCGGCCGGAGCAGATCATGAAG GCACAGCCAAGAGCGGTACCGGCATTGCGGCCGTGTCTGTCATGCGGCCGGAGCAGATCATGAAG A G AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding CDS,CDS,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2519201..2519275 26863196 MeRIP-seq:(Medium) rs760742093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45684,Human_RBP_ID_471310,Human_RBP_ID_762090,Human_RBP_ID_1515244,Human_RBP_ID_4358925,Human_RBP_ID_17874267,Human_RBP_ID_22052799,Human_RBP_ID_22441227,Human_RBP_ID_22800416,Human_RBP_ID_23684564,Human_RBP_ID_26941169,Human_RBP_ID_27239367 Human_Splice_Rec_1666300,Human_Splice_Rec_1666304,Human_Splice_Rec_1666308,Human_Splice_Rec_1666312 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779,RMVar_hsa_circ_106510,RMVar_hsa_circ_175781 73063 RMVar_ID_73063 Human_SNP_ID_591323031 m1A Human chr16 + 2519331 2519331 2519331 AGTCCATCATCCCAGTGGTCATGGCTGGCATCATCGCCATCTACGGCCTGGTGGTGGCAGTCCTC AGTCCATCATCCCAGTGGTCATGGCTGGCATCGTCGCCATCTACGGCCTGGTGGTGGCAGTCCTC A G AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding CDS,CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2519280..2519400 26863196 MeRIP-seq:(Medium) rs941952776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45684,Human_RBP_ID_471314,Human_RBP_ID_1003639,Human_RBP_ID_4358927,Human_RBP_ID_5142637,Human_RBP_ID_5259158,Human_RBP_ID_9061428,Human_RBP_ID_18189841,Human_RBP_ID_22441227,Human_RBP_ID_23684565,Human_RBP_ID_26941170,Human_RBP_ID_27239369 Human_Splice_Rec_1666301,Human_Splice_Rec_1666305,Human_Splice_Rec_1666309,Human_Splice_Rec_1666313,Human_Splice_Rec_1666315 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779,RMVar_hsa_circ_106510,RMVar_hsa_circ_175781 73064 RMVar_ID_73064 Human_SNP_ID_591323236 m1A Human chr16 + 2519784 2519784 2519784 TCCGAGCCCACCAGCCACAGAATATTATGTAAAGACCACCCCTCCTCATTCCAGAACGAACAGCC TCCGAGCCCACCAGCCACAGAATATTATGTAAGGACCACCCCTCCTCATTCCAGAACGAACAGCC A G AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding 3'UTR,3'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2519607..2519915 26863196 MeRIP-seq:(Medium) rs747329626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471324,Human_RBP_ID_1515253,Human_RBP_ID_1840419,Human_RBP_ID_3493426,Human_RBP_ID_8430684,Human_RBP_ID_12703982,Human_RBP_ID_17371244,Human_RBP_ID_17652886,Human_RBP_ID_18676027,Human_RBP_ID_18939910,Human_RBP_ID_21888714,Human_RBP_ID_23684567,Human_RBP_ID_26440257,Human_RBP_ID_27440558 Human_miRNA_ID_2153608,Human_miRNA_ID_2153609,Human_miRNA_ID_2801485,Human_miRNA_ID_2801486,Human_miRNA_ID_3009618,Human_miRNA_ID_3009619 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779,RMVar_hsa_circ_78257,RMVar_hsa_circ_106510,RMVar_hsa_circ_175781,RMVar_hsa_circ_175782 73065 RMVar_ID_73065 Human_SNP_ID_591323280 m1A Human chr16 - 2519885 2519885 2519885 GGCGGGCGGGGGCAAGGCCGGGGAAACAGACGATGGGCACTAGGACACTGCGCATGTACAAGACC GGCGGGCGGGGGCAAGGCCGGGGAAACAGACGGTGGGCACTAGGACACTGCGCATGTACAAGACC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:2519703..2519907 26863410 MeRIP-seq:(Medium) rs879054334 Functional Loss SNV dbSNP153 33..33 33 - - - 73066 RMVar_ID_73066 Human_SNP_ID_591323371 m1A Human chr16 + 2520043 2520041 2520043 TGTCATTTCTCTTTACTGGATGTTTATTTATAAAGATCTGGCCTGTTCCTGCGTCTGCGGAGCGG TGTCATTTCTCTTTACTGGATGTTTATTTAT__AGATCTGGCCTGTTCCTGCGTCTGCGGAGCGG TAA T AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding 3'UTR,3'UTR,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2520001..2520050 26863196 MeRIP-seq:(Medium) rs1023429890 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_45688,Human_RBP_ID_471325,Human_RBP_ID_1003645,Human_RBP_ID_1088473,Human_RBP_ID_1177516,Human_RBP_ID_1515260,Human_RBP_ID_1840423,Human_RBP_ID_3493428,Human_RBP_ID_4358954,Human_RBP_ID_5113324,Human_RBP_ID_8430687,Human_RBP_ID_9061431,Human_RBP_ID_12703994,Human_RBP_ID_17369282,Human_RBP_ID_17485813,Human_RBP_ID_17652888,Human_RBP_ID_18189843,Human_RBP_ID_18676033,Human_RBP_ID_21889064,Human_RBP_ID_22937279,Human_RBP_ID_23209240,Human_RBP_ID_23684568,Human_RBP_ID_24413035,Human_RBP_ID_24475857,Human_RBP_ID_26446668,Human_RBP_ID_26809892,Human_RBP_ID_27239379 Human_miRNA_ID_3088734,Human_miRNA_ID_3088735 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779,RMVar_hsa_circ_78257,RMVar_hsa_circ_106510,RMVar_hsa_circ_175781,RMVar_hsa_circ_175782 73067 RMVar_ID_73067 Human_SNP_ID_591323721 m1A Human chr16 - 2520427 2520427 2520427 TCGTGAGCCGTGTCGGGAGCGAGCGGCTCCGGAGCCCCGCGGCGGCCAAATCCCGCGCCCAGTGA TCGTGAGCCGTGTCGGGAGCGAGCGGCTCCGGGGCCCCGCGGCGGCCAAATCCCGCGCCCAGTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2520376..2520852 26863196 MeRIP-seq:(Medium) rs1261597974 Functional Loss SNV dbSNP153 33..33 33 - - - 73068 RMVar_ID_73068 Human_SNP_ID_591326796 m1A Human chr16 - 2528148 2528147 2528149 CAGCCCCGCCCCTGGGGCCCCATAGCACTCACAGGCAGCATGGCGTTGAAGAGGTGGGTGATGAA CAGCCCCGCCCCTGGGGCCCCATAGCACTCA__GGCAGCATGGCGTTGAAGAGGTGGGTGATGAA CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2528056..2528147 26863196 MeRIP-seq:(Medium) rs1476690937 Functional Loss DEL dbSNP153 32..33 33 - - - 73069 RMVar_ID_73069 Human_SNP_ID_591327419 m1A Human chr16 - 2529527 2529527 2529527 TGCCTAGCTGCGTCCGCCTGCCACACCAGCTCACCCGAGATGTAGGTGGCCTGGACGTGAAGGGA TGCCTAGCTGCGTCCGCCTGCCACACCAGCTCGCCCGAGATGTAGGTGGCCTGGACGTGAAGGGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2529338..2529686 32194978 MeRIP-seq:(Medium) rs1372425261 Functional Loss SNV dbSNP153 33..33 33 - - - 73070 RMVar_ID_73070 Human_SNP_ID_591327448 m1A Human chr16 + 2529584 2529584 2529584 GCTAGGCAGTGACAAGGACCTCGGCTGAGAGGACACCTGGCCGCAGCGGGATGCCATCAGGGCCG GCTAGGCAGTGACAAGGACCTCGGCTGAGAGGCCACCTGGCCGCAGCGGGATGCCATCAGGGCCG A C AMDHD2 Ensembl:ENSG00000162066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2529543..2530192 26863196 MeRIP-seq:(Medium) rs779576882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704184 73071 RMVar_ID_73071 Human_SNP_ID_591327449 m1A Human chr16 + 2529584 2529584 2529584 GCTAGGCAGTGACAAGGACCTCGGCTGAGAGGACACCTGGCCGCAGCGGGATGCCATCAGGGCCG GCTAGGCAGTGACAAGGACCTCGGCTGAGAGGGCACCTGGCCGCAGCGGGATGCCATCAGGGCCG A G AMDHD2 Ensembl:ENSG00000162066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2529543..2530192 26863196 MeRIP-seq:(Medium) rs779576882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704184 73072 RMVar_ID_73072 Human_SNP_ID_591327549 m1A Human chr16 + 2529895 2529895 2529895 GGGACAGGGCCTGTCTGCATGAAGTGGACCGGAGACCTGCAGACCCCAGGAAAGTGTCACTATGG GGGACAGGGCCTGTCTGCATGAAGTGGACCGGCGACCTGCAGACCCCAGGAAAGTGTCACTATGG A C AMDHD2 Ensembl:ENSG00000162066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2529784..2530063 26863196 MeRIP-seq:(Medium) rs113805498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763757,Human_RBP_ID_8184274,Human_RBP_ID_12704194,Human_RBP_ID_17883656 73073 RMVar_ID_73073 Human_SNP_ID_591327550 m1A Human chr16 + 2529895 2529895 2529895 GGGACAGGGCCTGTCTGCATGAAGTGGACCGGAGACCTGCAGACCCCAGGAAAGTGTCACTATGG GGGACAGGGCCTGTCTGCATGAAGTGGACCGGGGACCTGCAGACCCCAGGAAAGTGTCACTATGG A G AMDHD2 Ensembl:ENSG00000162066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2529784..2530063 26863196 MeRIP-seq:(Medium) rs113805498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763757,Human_RBP_ID_8184274,Human_RBP_ID_12704194,Human_RBP_ID_17883656 73074 RMVar_ID_73074 Human_SNP_ID_591328155 m1A Human chr16 - 2531048 2531048 2531048 GCTGAGGATGGGCACATCAAGCACTGACAGCCAGCAAGCTGGGCACAGGCGATGCTCAACCTCTA GCTGAGGATGGGCACATCAAGCACTGACAGCCGGCAAGCTGGGCACAGGCGATGCTCAACCTCTA T C CEMP1 Ensembl:ENSG00000205923 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2530082..2531273 32194978 MeRIP-seq:(Medium) rs538285962 Functional Loss SNV dbSNP153 33..33 33 - - - 73075 RMVar_ID_73075 Human_SNP_ID_591328251 m1A Human chr16 + 2531248 2531248 2531248 GTCGGGGAGGGGCTGGCAGAGATGGTTGGTCCACAGGGCTAGCCCTGGGTGGTGGGAGAGGGGCC GTCGGGGAGGGGCTGGCAGAGATGGTTGGTCCGCAGGGCTAGCCCTGGGTGGTGGGAGAGGGGCC A G AMDHD2 Ensembl:ENSG00000162066 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2531220..2531333 26863196 MeRIP-seq:(Medium) rs577306533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261380,Human_RBP_ID_3947174,Human_RBP_ID_8184275 Clinvar_Rec_318 73076 RMVar_ID_73076 Human_SNP_ID_591328286 m1A Human chr16 - 2531339 2531337 2531340 GCAAACCAAAACCAACCAAGAGTGCTTCCCCCACACCTCAAAATCATCCTGCAGCAGCTCCCTGG GCAAACCAAAACCAACCAAGAGTGCTTCCCC___ACCTCAAAATCATCCTGCAGCAGCTCCCTGG TGTG T CEMP1 Ensembl:ENSG00000205923 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2531240..2531356 26863196 MeRIP-seq:(Medium) rs1321264593 Functional Loss DEL dbSNP153 32..34 33 - - - 73077 RMVar_ID_73077 Human_SNP_ID_591330713 m1A Human chr16 - 2538054 2538054 2538054 CCCCGCAGCGCTGCGCGGCTCGGCGCCTCCTCAGCGTCCTCCTCCCCGAAGCGGAGCCCCAGCAA CCCCGCAGCGCTGCGCGGCTCGGCGCCTCCTCCGCGTCCTCCTCCCCGAAGCGGAGCCCCAGCAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:2538001..2538150;chr16:2538003..2538378 26863196 MeRIP-seq:(Medium) rs1198701326 Functional Loss SNV dbSNP153 33..33 33 - - - 73078 RMVar_ID_73078 Human_SNP_ID_591330745 m1A Human chr16 + 2538113 2538113 2538113 GCGGGGGAGGCGCCCGCGCCGACGCGGGGCCCATGGCCAGGACCACCAGCCAGCTGGTGAGCGCG GCGGGGGAGGCGCCCGCGCCGACGCGGGGCCCGTGGCCAGGACCACCAGCCAGCTGGTGAGCGCG A G PDPK1 Ensembl:ENSG00000140992 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:2538026..2538150 26863410 MeRIP-seq:(Medium) rs1283755886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891298,Human_RBP_ID_4393524,Human_RBP_ID_5317350,Human_RBP_ID_9372097,Human_RBP_ID_18418642,Human_RBP_ID_18985278,Human_RBP_ID_22581810,Human_RBP_ID_22944384,Human_RBP_ID_27810788 Human_Splice_Rec_1666517,Human_Splice_Rec_1666525,Human_Splice_Rec_1666547,Human_Splice_Rec_1666567,Human_Splice_Rec_1666571,Human_Splice_Rec_1666577,Human_Splice_Rec_1666583,Human_Splice_Rec_1666587 73079 RMVar_ID_73079 Human_SNP_ID_591331364 m1A Human chr16 + 2539709 2539709 2539709 CATGAATTAGGCGGATTGGCCAGGCTCAGTGGAGGCTGGGGCCGAGAGTTATGTCGAAGTTTGTG CATGAATTAGGCGGATTGGCCAGGCTCAGTGGGGGCTGGGGCCGAGAGTTATGTCGAAGTTTGTG A G PDPK1 Ensembl:ENSG00000140992 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2539707..2539816 26863196 MeRIP-seq:(Medium) rs987153405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704399 73080 RMVar_ID_73080 Human_SNP_ID_591345013 m1A Human chr16 - 2603503 2603503 2603503 ACCCCAACCCCGCCCCGAGCCTGCCACGGGCCAGCGGCAGGAGCTCGCAGTGATTCCCCGCCATG ACCCCAACCCCGCCCCGAGCCTGCCACGGGCCGGCGGCAGGAGCTCGCAGTGATTCCCCGCCATG T C lnc-CEMP1-10 RNACentral:URS00008B7AF1 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2603496..2603700 26863196 MeRIP-seq:(Medium) rs1377800083 Functional Loss SNV dbSNP153 33..33 33 - - - 73081 RMVar_ID_73081 Human_SNP_ID_591345123 m1A Human chr16 - 2603693 2603693 2603693 TGTCCGAGTCCGGGTCGGGGTCGGCCTGGCTCAAGAGGTACAGGAAGGATTTCGGGTCCTGACAC TGTCCGAGTCCGGGTCGGGGTCGGCCTGGCTCTAGAGGTACAGGAAGGATTTCGGGTCCTGACAC T A lnc-CEMP1-10 RNACentral:URS00008B7AF1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2603644..2610477 26863196 MeRIP-seq:(Medium) rs567362513 Functional Loss SNV dbSNP153 33..33 33 - - - 73082 RMVar_ID_73082 Human_SNP_ID_591345124 m1A Human chr16 - 2603693 2603693 2603693 TGTCCGAGTCCGGGTCGGGGTCGGCCTGGCTCAAGAGGTACAGGAAGGATTTCGGGTCCTGACAC TGTCCGAGTCCGGGTCGGGGTCGGCCTGGCTCCAGAGGTACAGGAAGGATTTCGGGTCCTGACAC T G lnc-CEMP1-10 RNACentral:URS00008B7AF1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2603644..2610477 26863196 MeRIP-seq:(Medium) rs567362513 Functional Loss SNV dbSNP153 33..33 33 - - - 73083 RMVar_ID_73083 Human_SNP_ID_591361713 m1A Human chr16 - 2682630 2682630 2682630 GCGCTGGGCCAGGGCGCCGAGCCCAGCGCTGCAGCGGCGGCACAGGCCGCCCCCCAGCCCCGCCC GCGCTGGGCCAGGGCGCCGAGCCCAGCGCTGCCGCGGCGGCACAGGCCGCCCCCCAGCCCCGCCC T G lnc-PRSS27-2 RNACentral:URS00008B6036 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2682581..2682694 26863196 MeRIP-seq:(Medium) rs1246301829 Functional Loss SNV dbSNP153 33..33 33 - - - 73084 RMVar_ID_73084 Human_SNP_ID_591369048 m1A Human chr16 - 2706698 2706698 2706698 CCCTCCTCATCTGTACCACGTCAGCCCTGCAGAGCCCACGGCCCCTCGGCCCCCTGCCCTCCCCA CCCTCCTCATCTGTACCACGTCAGCCCTGCAGGGCCCACGGCCCCTCGGCCCCCTGCCCTCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2706696..2706846 26863196 MeRIP-seq:(Medium) rs1248693363 Functional Loss SNV dbSNP153 33..33 33 - - - 73085 RMVar_ID_73085 Human_SNP_ID_591369049 m1A Human chr16 - 2706698 2706698 2706698 CCCTCCTCATCTGTACCACGTCAGCCCTGCAGAGCCCACGGCCCCTCGGCCCCCTGCCCTCCCCA CCCTCCTCATCTGTACCACGTCAGCCCTGCAGCGCCCACGGCCCCTCGGCCCCCTGCCCTCCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2706696..2706846 26863196 MeRIP-seq:(Medium) rs1248693363 Functional Loss SNV dbSNP153 33..33 33 - - - 73086 RMVar_ID_73086 Human_SNP_ID_591372336 m1A Human chr16 - 2716256 2716256 2716256 GTGCAGGATGAGGGCGGCAGGGTCTGAGGATCACCCTGAACCGTGACTGGCCCCCTCTGGGTGGC GTGCAGGATGAGGGCGGCAGGGTCTGAGGATCGCCCTGAACCGTGACTGGCCCCCTCTGGGTGGC T C PRSS27 Ensembl:ENSG00000172382 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2716254..2716461 26863196 MeRIP-seq:(Medium) rs748320061 Functional Loss SNV dbSNP153 33..33 33 - - - 73087 RMVar_ID_73087 Human_SNP_ID_591379188 m1A Human chr16 - 2739970 2739969 2739970 TGTTTGCAAGGTAGGTCAGGTGACAGGGAGCCAGGGGGGCTGAGGAGGCTCAGGGCCTGACTCCA TGTTTGCAAGGTAGGTCAGGTGACAGGGAGCC_GGGGGGCTGAGGAGGCTCAGGGCCTGACTCCA CT C SRRM2-AS1 Ensembl:ENSG00000205913 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2739966..2740037 26863196 MeRIP-seq:(Medium) rs1328195493 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_235306,Human_RBP_ID_3509881 73088 RMVar_ID_73088 Human_SNP_ID_591379189 m1A Human chr16 - 2739970 2739970 2739970 TGTTTGCAAGGTAGGTCAGGTGACAGGGAGCCAGGGGGGCTGAGGAGGCTCAGGGCCTGACTCCA TGTTTGCAAGGTAGGTCAGGTGACAGGGAGCCGGGGGGGCTGAGGAGGCTCAGGGCCTGACTCCA T C SRRM2-AS1 Ensembl:ENSG00000205913 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2739966..2740037 26863196 MeRIP-seq:(Medium) rs1446245768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235306,Human_RBP_ID_3509881 73089 RMVar_ID_73089 Human_SNP_ID_591383690 m1A Human chr16 + 2752712 2752712 2752712 AGTTGGAGCCCGTTGCGGCCCCTGAGGAAGCGAGGAGGCGTCGGCGTCGGCTGAGGCGGGCGGAC AGTTGGAGCCCGTTGCGGCCCCTGAGGAAGCGGGGAGGCGTCGGCGTCGGCTGAGGCGGGCGGAC A G SRRM2 Ensembl:ENSG00000167978 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2752626..2752907;chr16:2752626..2752936 26863196 MeRIP-seq:(Medium) rs1331307086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46297,Human_RBP_ID_235049,Human_RBP_ID_4359721,Human_RBP_ID_5571595,Human_RBP_ID_9324884,Human_RBP_ID_9373668,Human_RBP_ID_17874501,Human_RBP_ID_18418905,Human_RBP_ID_18469652,Human_RBP_ID_18985281,Human_RBP_ID_22532654,Human_RBP_ID_24544350,Human_RBP_ID_24558711,Human_RBP_ID_27810790 73090 RMVar_ID_73090 Human_SNP_ID_591383695 m1A Human chr16 - 2752720 2752715 2752721 CCTCGCCGGTCCGCCCGCCTCAGCCGACGCCGACGCCTCCTCGCTTCCTCAGGGGCCGCAACGGG CCTCGCCGGTCCGCCCGCCTCAGCCGACGCC______TCCTCGCTTCCTCAGGGGCCGCAACGGG AGGCGTC A SRRM2-AS1,SRRM2-AS1:2,SRRM2-AS1:3,SRRM2-AS1:4,SRRM2-AS1:5,SRRM2-AS1:6 RNACentral:URS0000D5BFCE,RNACentral:URS0000D58BE7,RNACentral:URS0000D5D43A,RNACentral:URS00008B64EC,RNACentral:URS0000D58EB3,RNACentral:URS0000D59513 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2752676..2752916 26863196 MeRIP-seq:(Medium) rs1268842194 Functional Loss DEL dbSNP153 32..37 33 - - - 73091 RMVar_ID_73091 Human_SNP_ID_591383780 m1A Human chr16 - 2752848 2752835 2752848 CCCACCCGGCTCGCTGGCTCCCTCACCCTCTCACCCGCCGCCTCCGCCCGCCGCCTCCGAGGGGG CCCACCCGGCTCGCTGGCTCCCTCACCCTCTC_____________GCCCGCCGCCTCCGAGGGGG CGGAGGCGGCGGGT C SRRM2-AS1,SRRM2-AS1:2,SRRM2-AS1:3,SRRM2-AS1:4,SRRM2-AS1:5,SRRM2-AS1:6 RNACentral:URS0000D5BFCE,RNACentral:URS0000D58BE7,RNACentral:URS0000D5D43A,RNACentral:URS00008B64EC,RNACentral:URS0000D58EB3,RNACentral:URS0000D59513 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2752626..2752945;chr16:2752626..2753465 26863196 MeRIP-seq:(Medium) rs764629554 Functional Loss DEL dbSNP153 33..45 33 - - - 73092 RMVar_ID_73092 Human_SNP_ID_591383787 m1A Human chr16 - 2752848 2752848 2752848 CCCACCCGGCTCGCTGGCTCCCTCACCCTCTCACCCGCCGCCTCCGCCCGCCGCCTCCGAGGGGG CCCACCCGGCTCGCTGGCTCCCTCACCCTCTCGCCCGCCGCCTCCGCCCGCCGCCTCCGAGGGGG T C SRRM2-AS1,SRRM2-AS1:2,SRRM2-AS1:3,SRRM2-AS1:4,SRRM2-AS1:5,SRRM2-AS1:6 RNACentral:URS0000D5BFCE,RNACentral:URS0000D58BE7,RNACentral:URS0000D5D43A,RNACentral:URS00008B64EC,RNACentral:URS0000D58EB3,RNACentral:URS0000D59513 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2752626..2752945;chr16:2752626..2753465 26863196 MeRIP-seq:(Medium) rs1046890702 Functional Loss SNV dbSNP153 33..33 33 - - - 73093 RMVar_ID_73093 Human_SNP_ID_591383788 m1A Human chr16 - 2752848 2752848 2752848 CCCACCCGGCTCGCTGGCTCCCTCACCCTCTCACCCGCCGCCTCCGCCCGCCGCCTCCGAGGGGG CCCACCCGGCTCGCTGGCTCCCTCACCCTCTCCCCCGCCGCCTCCGCCCGCCGCCTCCGAGGGGG T G SRRM2-AS1,SRRM2-AS1:2,SRRM2-AS1:3,SRRM2-AS1:4,SRRM2-AS1:5,SRRM2-AS1:6 RNACentral:URS0000D5BFCE,RNACentral:URS0000D58BE7,RNACentral:URS0000D5D43A,RNACentral:URS00008B64EC,RNACentral:URS0000D58EB3,RNACentral:URS0000D59513 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2752626..2752945;chr16:2752626..2753465 26863196 MeRIP-seq:(Medium) rs1046890702 Functional Loss SNV dbSNP153 33..33 33 - - - 73094 RMVar_ID_73094 Human_SNP_ID_591384764 m1A Human chr16 - 2754649 2754649 2754649 GACCTGCACTTAATTCTTCAGCTTAACCATTCACCCACACTTCCATACCACCTCACACAAAAATC GACCTGCACTTAATTCTTCAGCTTAACCATTCTCCCACACTTCCATACCACCTCACACAAAAATC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2754645..2754728 26863196 MeRIP-seq:(Medium) rs1166361642 Functional Loss SNV dbSNP153 33..33 33 - - - 73095 RMVar_ID_73095 Human_SNP_ID_591384972 m1A Human chr16 + 2755153 2755153 2755153 ATCTTGGAGAGGATGAGGGTGAGAAAGAGAGTATATGTAATAGGAGAAAGGAATAGAGTATGTGT ATCTTGGAGAGGATGAGGGTGAGAAAGAGAGTGTATGTAATAGGAGAAAGGAATAGAGTATGTGT A G SRRM2 Ensembl:ENSG00000167978 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2755151..2755563;chr16:2755151..2755537 26863196 MeRIP-seq:(Medium) rs564000329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12708214,Human_RBP_ID_22937462,Human_RBP_ID_23685075 73096 RMVar_ID_73096 Human_SNP_ID_591385291 m1A Human chr16 + 2756008 2756008 2756008 CAAAGGAGAACAAAAAGGGACAGTGTGGAGAGATTTTAGAGGAACAAGATCCTTGTTTGCCTAGG CAAAGGAGAACAAAAAGGGACAGTGTGGAGAGGTTTTAGAGGAACAAGATCCTTGTTTGCCTAGG A G SRRM2 Ensembl:ENSG00000167978 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2756006..2757063 26863196 MeRIP-seq:(Medium) rs1268349770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9823885,Human_RBP_ID_12708274 73097 RMVar_ID_73097 Human_SNP_ID_591385367 m1A Human chr16 + 2756280 2756280 2756280 GAAGGAGAGCAGGGACTTGGGTGTGGGGCGGTAAGTGGTTAGTTTGGGGCCAGGGGCCTGACCCG GAAGGAGAGCAGGGACTTGGGTGTGGGGCGGTGAGTGGTTAGTTTGGGGCCAGGGGCCTGACCCG A G SRRM2 Ensembl:ENSG00000167978 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2756277..2756659 26863196 MeRIP-seq:(Medium) rs1372157499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1281563,Human_RBP_ID_5182470,Human_RBP_ID_22581823 73098 RMVar_ID_73098 Human_SNP_ID_591385369 m1A Human chr16 - 2756286 2756286 2756286 GAGACACGGGTCAGGCCCCTGGCCCCAAACTAACCACTTACCGCCCCACACCCAAGTCCCTGCTC GAGACACGGGTCAGGCCCCTGGCCCCAAACTAGCCACTTACCGCCCCACACCCAAGTCCCTGCTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2756283..2756670 26863196 MeRIP-seq:(Medium) rs973941028 Functional Loss SNV dbSNP153 33..33 33 - - - 73099 RMVar_ID_73099 Human_SNP_ID_591386015 m1A Human chr16 - 2757742 2757741 2757742 AAAAGAAGGGCAAAAGTCTGAAGGAAATATAAAGGACAGAGCCATATTCAGAACACAAGTATAAG AAAAGAAGGGCAAAAGTCTGAAGGAAATATAA_GGACAGAGCCATATTCAGAACACAAGTATAAG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2757738..2757984 26863196 MeRIP-seq:(Medium) rs1176884239 Functional Loss DEL dbSNP153 33..33 33 - - - 73100 RMVar_ID_73100 Human_SNP_ID_591386029 m1A Human chr16 - 2757763 2757763 2757763 TGAGTCTCCGTGACCCTAGAGAAAAGAAGGGCAAAAGTCTGAAGGAAATATAAAGGACAGAGCCA TGAGTCTCCGTGACCCTAGAGAAAAGAAGGGCTAAAGTCTGAAGGAAATATAAAGGACAGAGCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2757761..2757891 26863196 MeRIP-seq:(Medium) rs768967729 Functional Loss SNV dbSNP153 33..33 33 - - - 73101 RMVar_ID_73101 Human_SNP_ID_591386030 m1A Human chr16 - 2757763 2757763 2757763 TGAGTCTCCGTGACCCTAGAGAAAAGAAGGGCAAAAGTCTGAAGGAAATATAAAGGACAGAGCCA TGAGTCTCCGTGACCCTAGAGAAAAGAAGGGCGAAAGTCTGAAGGAAATATAAAGGACAGAGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2757761..2757891 26863196 MeRIP-seq:(Medium) rs768967729 Functional Loss SNV dbSNP153 33..33 33 - - - 73102 RMVar_ID_73102 Human_SNP_ID_591386598 m1A Human chr16 - 2759128 2759126 2759128 TTCTTGGACTCAGATTCTGACCTGTTGGAAAAAAGAGAAGAAAAAACATAAGAAACACCTCTGCC TTCTTGGACTCAGATTCTGACCTGTTGGAAAA__GAGAAGAAAAAACATAAGAAACACCTCTGCC CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2759126..2759175 26863196 MeRIP-seq:(Medium) rs765627602 Functional Loss DEL dbSNP153 33..34 33 - - - 73103 RMVar_ID_73103 Human_SNP_ID_591386600 m1A Human chr16 - 2759128 2759128 2759128 TTCTTGGACTCAGATTCTGACCTGTTGGAAAAAAGAGAAGAAAAAACATAAGAAACACCTCTGCC TTCTTGGACTCAGATTCTGACCTGTTGGAAAAGAGAGAAGAAAAAACATAAGAAACACCTCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2759126..2759175 26863196 MeRIP-seq:(Medium) rs778433960 Functional Loss SNV dbSNP153 33..33 33 - - - 73104 RMVar_ID_73104 Human_SNP_ID_591387187 m1A Human chr16 - 2760412 2760412 2760412 GTCTCCGGGCTACTAGGCCGTTGTGTGCTGGTAGTACCTGGTTCACTGAAAGGCGCATCTCCCTC GTCTCCGGGCTACTAGGCCGTTGTGTGCTGGTGGTACCTGGTTCACTGAAAGGCGCATCTCCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2760362..2760432 26863196 MeRIP-seq:(Medium) rs538525400 Functional Loss SNV dbSNP153 33..33 33 - - - 73105 RMVar_ID_73105 Human_SNP_ID_591387242 m1A Human chr16 + 2760491 2760491 2760491 CTAGCAGCCCTTATGAAGACAAAGATAAAGACAAGAAGGAGGTATGTTCCTGAGTTGGTGATGTT CTAGCAGCCCTTATGAAGACAAAGATAAAGACGAGAAGGAGGTATGTTCCTGAGTTGGTGATGTT A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2760476..2760500 26863196 MeRIP-seq:(Medium) rs1173122145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515431,Human_RBP_ID_1840635,Human_RBP_ID_5113333,Human_RBP_ID_9372111,Human_RBP_ID_12708420,Human_RBP_ID_26328526 Human_Splice_Rec_1667117,Human_Splice_Rec_1667135,Human_Splice_Rec_1667155,Human_Splice_Rec_1667199,Human_Splice_Rec_1667223,Human_Splice_Rec_1667271,Human_Splice_Rec_1667275,Human_Splice_Rec_1667277 RMVar_hsa_circ_101161,RMVar_hsa_circ_342974,RMVar_hsa_circ_175801,RMVar_hsa_circ_283429,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_175806,RMVar_hsa_circ_335976,RMVar_hsa_circ_77021,RMVar_hsa_circ_175810,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_53306,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_265651 73106 RMVar_ID_73106 Human_SNP_ID_591387756 m1A Human chr16 - 2761650 2761650 2761650 GGGGTGGTTGCAAGGGGTTGTGGGGAGCCGCCATGTCGCTCAGCAAGGAGCGGAGTGGGAGCAGG GGGGTGGTTGCAAGGGGTTGTGGGGAGCCGCCGTGTCGCTCAGCAAGGAGCGGAGTGGGAGCAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:2761601..2761982;chr16:2761601..2761875 26863196 MeRIP-seq:(Medium) rs1252574977 Functional Loss SNV dbSNP153 33..33 33 - - - 73107 RMVar_ID_73107 Human_SNP_ID_591387772 m1A Human chr16 + 2761678 2761678 2761678 GACATGGCGGCTCCCCACAACCCCTTGCAACCACCCCCTTAAGCCAGGAGCCAGTGAACCCCCCA GACATGGCGGCTCCCCACAACCCCTTGCAACCTCCCCCTTAAGCCAGGAGCCAGTGAACCCCCCA A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2761576..2761750 26863410 MeRIP-seq:(Medium) rs750629473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1003686,Human_RBP_ID_6505251,Human_RBP_ID_17077825,Human_RBP_ID_22052813,Human_RBP_ID_22199192,Human_RBP_ID_22800503,Human_RBP_ID_22937583 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73108 RMVar_ID_73108 Human_SNP_ID_591387797 m1A Human chr16 - 2761711 2761711 2761711 TGGTGAACGGTCCCGAGTTGGAGAGGCCTCAGATGGGGGGTTCACTGGCTCCTGGCTTAAGGGGG TGGTGAACGGTCCCGAGTTGGAGAGGCCTCAGTTGGGGGGTTCACTGGCTCCTGGCTTAAGGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2761547..2763661 26863196 MeRIP-seq:(Medium) rs140983799 Functional Loss SNV dbSNP153 33..33 33 - - - 73109 RMVar_ID_73109 Human_SNP_ID_591387798 m1A Human chr16 - 2761711 2761711 2761711 TGGTGAACGGTCCCGAGTTGGAGAGGCCTCAGATGGGGGGTTCACTGGCTCCTGGCTTAAGGGGG TGGTGAACGGTCCCGAGTTGGAGAGGCCTCAGGTGGGGGGTTCACTGGCTCCTGGCTTAAGGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2761547..2763661 26863196 MeRIP-seq:(Medium) rs140983799 Functional Loss SNV dbSNP153 33..33 33 - - - 73110 RMVar_ID_73110 Human_SNP_ID_591388282 m1A Human chr16 - 2762473 2762473 2762473 GCGTGAGCGGCCACGTCTAGCTGGGGTTCTAGAGCGTGACCTGCCACTTCTCCTGGCTGGTGATC GCGTGAGCGGCCACGTCTAGCTGGGGTTCTAGTGCGTGACCTGCCACTTCTCCTGGCTGGTGATC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2762424..2762630 26863196 MeRIP-seq:(Medium) rs1198531011 Functional Loss SNV dbSNP153 33..33 33 - - - 73111 RMVar_ID_73111 Human_SNP_ID_591388396 m1A Human chr16 + 2762625 2762623 2762626 AGAGGGAGGTCTCGGTCTAGGACACCAAGACGAGGAAGATCCCGCAGTAGAAGCTTAGTTAGACG AGAGGGAGGTCTCGGTCTAGGACACCAAGAC___GAAGATCCCGCAGTAGAAGCTTAGTTAGACG CGAG C SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2762576..2762650 26863196 MeRIP-seq:(Medium) rs781229628 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_818613,Human_RBP_ID_1515510,Human_RBP_ID_1840690,Human_RBP_ID_3493642,Human_RBP_ID_5571617,Human_RBP_ID_6505300,Human_RBP_ID_8431026,Human_RBP_ID_9823953,Human_RBP_ID_12708834,Human_RBP_ID_17689971,Human_RBP_ID_18529704,Human_RBP_ID_18676440,Human_RBP_ID_20093630,Human_RBP_ID_26329692 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73112 RMVar_ID_73112 Human_SNP_ID_591388398 m1A Human chr16 + 2762625 2762625 2762625 AGAGGGAGGTCTCGGTCTAGGACACCAAGACGAGGAAGATCCCGCAGTAGAAGCTTAGTTAGACG AGAGGGAGGTCTCGGTCTAGGACACCAAGACGGGGAAGATCCCGCAGTAGAAGCTTAGTTAGACG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2762576..2762650 26863196 MeRIP-seq:(Medium) rs1453712613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818613,Human_RBP_ID_1515510,Human_RBP_ID_1840690,Human_RBP_ID_3493642,Human_RBP_ID_5571617,Human_RBP_ID_6505300,Human_RBP_ID_8431026,Human_RBP_ID_9823953,Human_RBP_ID_12708834,Human_RBP_ID_17689971,Human_RBP_ID_18529704,Human_RBP_ID_18676440,Human_RBP_ID_20093630,Human_RBP_ID_26329692 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73113 RMVar_ID_73113 Human_SNP_ID_591388556 m1A Human chr16 - 2762851 2762851 2762851 GCATGGGGAAGACCCTGAAAGGCTGCGCCTCAAAGACAAGCGAGATTTTGCTTTGGACCGTGGTG GCATGGGGAAGACCCTGAAAGGCTGCGCCTCAGAGACAAGCGAGATTTTGCTTTGGACCGTGGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2762801..2763100 26863196 MeRIP-seq:(Medium) rs1415595060 Functional Loss SNV dbSNP153 33..33 33 - - - 73114 RMVar_ID_73114 Human_SNP_ID_591388576 m1A Human chr16 + 2762880 2762880 2762880 TCTTTGAGGCGCAGCCTTTCAGGGTCTTCCCCATGCCCTAAACAAAAGTCACAGACACCACCCAG TCTTTGAGGCGCAGCCTTTCAGGGTCTTCCCCGTGCCCTAAACAAAAGTCACAGACACCACCCAG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2762833..2763063 26863196 MeRIP-seq:(Medium) rs1481294230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515520,Human_RBP_ID_6505316,Human_RBP_ID_8806337,Human_RBP_ID_9284578,Human_RBP_ID_17485862,Human_RBP_ID_18676450,Human_RBP_ID_22053837,Human_RBP_ID_22199226,Human_RBP_ID_22937627,Human_RBP_ID_24475918,Human_RBP_ID_24544365,Human_RBP_ID_25202585,Human_RBP_ID_26941662 Human_miRNA_ID_2376747,Human_miRNA_ID_2493572,Human_miRNA_ID_2695984,Human_miRNA_ID_3032397 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73115 RMVar_ID_73115 Human_SNP_ID_591388593 m1A Human chr16 + 2762911 2762911 2762911 CATGCCCTAAACAAAAGTCACAGACACCACCCAGGCGCAGTCGCTCTGGATCCTCCCAACCTAAA CATGCCCTAAACAAAAGTCACAGACACCACCCTGGCGCAGTCGCTCTGGATCCTCCCAACCTAAA A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2762863..2763068 26863196 MeRIP-seq:(Medium) rs369466610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761867,Human_RBP_ID_1515521,Human_RBP_ID_1840702,Human_RBP_ID_4359991,Human_RBP_ID_6505317,Human_RBP_ID_8431037,Human_RBP_ID_8806344,Human_RBP_ID_9061553,Human_RBP_ID_9823964,Human_RBP_ID_17253660,Human_RBP_ID_17369322,Human_RBP_ID_18676457,Human_RBP_ID_22497540,Human_RBP_ID_22945580,Human_RBP_ID_25243426,Human_RBP_ID_27239667,Human_RBP_ID_27440765 Human_miRNA_ID_2825610,Human_miRNA_ID_2859581 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73116 RMVar_ID_73116 Human_SNP_ID_591388611 m1A Human chr16 + 2762941 2762935 2762941 CCAGGCGCAGTCGCTCTGGATCCTCCCAACCTAAAGCTAAATCTAGAACGCCACCCAGACGCAGT CCAGGCGCAGTCGCTCTGGATCCTCCC______AAGCTAAATCTAGAACGCCACCCAGACGCAGT CAACCTA C SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2762851..2763070 26863196 MeRIP-seq:(Medium) rs1158449340 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_1365377,Human_RBP_ID_1840704,Human_RBP_ID_2472251,Human_RBP_ID_5571620,Human_RBP_ID_6505319,Human_RBP_ID_8431039,Human_RBP_ID_8806346,Human_RBP_ID_9061554,Human_RBP_ID_9284580,Human_RBP_ID_12708896,Human_RBP_ID_18676457,Human_RBP_ID_20093633,Human_RBP_ID_22937629,Human_RBP_ID_26440387,Human_RBP_ID_27440767 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73117 RMVar_ID_73117 Human_SNP_ID_591388611 m1A Human chr16 - 2762940 2762935 2762941 CTGCGTCTGGGTGGCGTTCTAGATTTAGCTTTAGGTTGGGAGGATCCAGAGCGACTGCGCCTGGG CTGCGTCTGGGTGGCGTTCTAGATTTAGCTT______GGGAGGATCCAGAGCGACTGCGCCTGGG CAACCTA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2762889..2763044 26863196 MeRIP-seq:(Medium) rs1158449340 Functional Loss DEL dbSNP153 32..37 33 - - - 73118 RMVar_ID_73118 Human_SNP_ID_591388612 m1A Human chr16 - 2762940 2762937 2762940 CTGCGTCTGGGTGGCGTTCTAGATTTAGCTTTAGGTTGGGAGGATCCAGAGCGACTGCGCCTGGG CTGCGTCTGGGTGGCGTTCTAGATTTAGCTTT___TTGGGAGGATCCAGAGCGACTGCGCCTGGG ACCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2762889..2763044 26863196 MeRIP-seq:(Medium) rs1397324967 Functional Loss DEL dbSNP153 33..35 33 - - - 73119 RMVar_ID_73119 Human_SNP_ID_591388638 m1A Human chr16 + 2762980 2762980 2762980 AATCTAGAACGCCACCCAGACGCAGTCGCTCCAGTTCTTCTCCGCCACCTAAACAGAAATCTAAG AATCTAGAACGCCACCCAGACGCAGTCGCTCCGGTTCTTCTCCGCCACCTAAACAGAAATCTAAG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2762835..2763036 26863196 MeRIP-seq:(Medium) rs1332683009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761868,Human_RBP_ID_1515523,Human_RBP_ID_1840705,Human_RBP_ID_3493651,Human_RBP_ID_6505320,Human_RBP_ID_8806346,Human_RBP_ID_9284581,Human_RBP_ID_12708896,Human_RBP_ID_17253663,Human_RBP_ID_17369323,Human_RBP_ID_17485865,Human_RBP_ID_18676457,Human_RBP_ID_20093634,Human_RBP_ID_22199231,Human_RBP_ID_22800525,Human_RBP_ID_22937630,Human_RBP_ID_25202592,Human_RBP_ID_26941671,Human_RBP_ID_27440769 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73120 RMVar_ID_73120 Human_SNP_ID_591388639 m1A Human chr16 + 2762980 2762980 2762980 AATCTAGAACGCCACCCAGACGCAGTCGCTCCAGTTCTTCTCCGCCACCTAAACAGAAATCTAAG AATCTAGAACGCCACCCAGACGCAGTCGCTCCTGTTCTTCTCCGCCACCTAAACAGAAATCTAAG A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2762835..2763036 26863196 MeRIP-seq:(Medium) rs1332683009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761868,Human_RBP_ID_1515523,Human_RBP_ID_1840705,Human_RBP_ID_3493651,Human_RBP_ID_6505320,Human_RBP_ID_8806346,Human_RBP_ID_9284581,Human_RBP_ID_12708896,Human_RBP_ID_17253663,Human_RBP_ID_17369323,Human_RBP_ID_17485865,Human_RBP_ID_18676457,Human_RBP_ID_20093634,Human_RBP_ID_22199231,Human_RBP_ID_22800525,Human_RBP_ID_22937630,Human_RBP_ID_25202592,Human_RBP_ID_26941671,Human_RBP_ID_27440769 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73121 RMVar_ID_73121 Human_SNP_ID_591388948 m1A Human chr16 + 2763475 2763475 2763475 CCTCCTCACCAGATACCAAAGTGAAACCTGAAACACCGCCAAGACAAAGTCACTCAGGGTCTATT CCTCCTCACCAGATACCAAAGTGAAACCTGAAGCACCGCCAAGACAAAGTCACTCAGGGTCTATT A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2763451..2763475 26863196 MeRIP-seq:(Medium) rs1238322919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515535,Human_RBP_ID_1840705,Human_RBP_ID_3493664,Human_RBP_ID_8431061,Human_RBP_ID_12708979,Human_RBP_ID_17255830,Human_RBP_ID_18676468,Human_RBP_ID_27239677 Human_miRNA_ID_2376748 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73122 RMVar_ID_73122 Human_SNP_ID_591389142 m1A Human chr16 + 2763804 2763804 2763804 GAATCACCATCTCTGCAGAGCAAATCTCAAACATCACCTAAGGGAGGTCGGTCCAGGTCTTCATC GAATCACCATCTCTGCAGAGCAAATCTCAAACGTCACCTAAGGGAGGTCGGTCCAGGTCTTCATC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2763753..2763838 26863196 MeRIP-seq:(Medium) rs780427323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471534,Human_RBP_ID_761872,Human_RBP_ID_1003718,Human_RBP_ID_1515558,Human_RBP_ID_1840723,Human_RBP_ID_3493667,Human_RBP_ID_4360032,Human_RBP_ID_5524839,Human_RBP_ID_6505361,Human_RBP_ID_8088599,Human_RBP_ID_8252031,Human_RBP_ID_8431079,Human_RBP_ID_8806384,Human_RBP_ID_9061561,Human_RBP_ID_9256734,Human_RBP_ID_9284608,Human_RBP_ID_9372116,Human_RBP_ID_12709044,Human_RBP_ID_17253685,Human_RBP_ID_17369338,Human_RBP_ID_17485883,Human_RBP_ID_17689974,Human_RBP_ID_17874583,Human_RBP_ID_18285114,Human_RBP_ID_18529717,Human_RBP_ID_18676476,Human_RBP_ID_20093641,Human_RBP_ID_22199243,Human_RBP_ID_26328037,Human_RBP_ID_26810939,Human_RBP_ID_26941683,Human_RBP_ID_27440785 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73123 RMVar_ID_73123 Human_SNP_ID_591389333 m1A Human chr16 + 2764165 2764165 2764165 TCAAAGACACACTTAGAACCCCGCCAAGGGAAAGAAGTGGTGCTGGGTCATCTCCAGAAACAAAA TCAAAGACACACTTAGAACCCCGCCAAGGGAAGGAAGTGGTGCTGGGTCATCTCCAGAAACAAAA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2764115..2764239 26863196 MeRIP-seq:(Medium) rs1300361752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45331,Human_RBP_ID_1527349,Human_RBP_ID_1840734,Human_RBP_ID_4360053,Human_RBP_ID_5523995,Human_RBP_ID_8806406,Human_RBP_ID_9256917,Human_RBP_ID_9372117,Human_RBP_ID_17371618,Human_RBP_ID_18676506,Human_RBP_ID_20093646,Human_RBP_ID_22053845,Human_RBP_ID_22800543,Human_RBP_ID_23685202,Human_RBP_ID_24544366,Human_RBP_ID_26329699,Human_RBP_ID_26941691 Human_miRNA_ID_134519,Human_miRNA_ID_301194,Human_miRNA_ID_1381731,Human_miRNA_ID_2065699,Human_miRNA_ID_2301156,Human_miRNA_ID_2304418,Human_miRNA_ID_2307685 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73124 RMVar_ID_73124 Human_SNP_ID_591389786 m1A Human chr16 + 2764959 2764959 2764959 AAAGATATACCTAGAACGCCATCTAGAGGGAGAAGCGAATGTGATTCTTCCCCAGAACCGAAAGC AAAGATATACCTAGAACGCCATCTAGAGGGAGCAGCGAATGTGATTCTTCCCCAGAACCGAAAGC A C SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1415789866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45335,Human_RBP_ID_1515592,Human_RBP_ID_1840738,Human_RBP_ID_3493691,Human_RBP_ID_8806443,Human_RBP_ID_9256923,Human_RBP_ID_18676512,Human_RBP_ID_20093654,Human_RBP_ID_23685220,Human_RBP_ID_25243449,Human_RBP_ID_26941709 Human_miRNA_ID_2022572,Human_miRNA_ID_2261113,Human_miRNA_ID_2264159,Human_miRNA_ID_2267226 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73125 RMVar_ID_73125 Human_SNP_ID_591390191 m1A Human chr16 + 2765634 2765634 2765634 CGATCATCTCCGGAGCTAACAAGGAAGGCCAGACTGTCCCGTAGAAGCCGCTCTGCCTCATCCTC CGATCATCTCCGGAGCTAACAAGGAAGGCCAGGCTGTCCCGTAGAAGCCGCTCTGCCTCATCCTC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2765583..2765826 26863196 MeRIP-seq:(Medium) rs933246362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471563,Human_RBP_ID_1515630,Human_RBP_ID_1840755,Human_RBP_ID_6505506,Human_RBP_ID_8431150,Human_RBP_ID_8806472,Human_RBP_ID_12709573,Human_RBP_ID_17253709,Human_RBP_ID_17369361,Human_RBP_ID_17485910,Human_RBP_ID_18676576,Human_RBP_ID_22937700,Human_RBP_ID_27239713 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73126 RMVar_ID_73126 Human_SNP_ID_591390212 m1A Human chr16 + 2765674 2765674 2765674 GTAGAAGCCGCTCTGCCTCATCCTCACCAGAAACTCGCTCTAGAACTCCCCCAAGGCACCGGAGA GTAGAAGCCGCTCTGCCTCATCCTCACCAGAAGCTCGCTCTAGAACTCCCCCAAGGCACCGGAGA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2765624..2766416 26863196 MeRIP-seq:(Medium) rs1352997335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45338,Human_RBP_ID_1515631,Human_RBP_ID_1840755,Human_RBP_ID_3493704,Human_RBP_ID_5180623,Human_RBP_ID_6505506,Human_RBP_ID_8083081,Human_RBP_ID_8431151,Human_RBP_ID_8806472,Human_RBP_ID_9284640,Human_RBP_ID_12709573,Human_RBP_ID_17253709,Human_RBP_ID_17369361,Human_RBP_ID_17485910,Human_RBP_ID_18411374,Human_RBP_ID_18676578,Human_RBP_ID_26941724,Human_RBP_ID_27239714,Human_RBP_ID_27440821 Human_miRNA_ID_2797911,Human_miRNA_ID_2798877,Human_miRNA_ID_2800258,Human_miRNA_ID_2807573,Human_miRNA_ID_2810717,Human_miRNA_ID_2813859,Human_miRNA_ID_2833449,Human_miRNA_ID_2852972,Human_miRNA_ID_2854034,Human_miRNA_ID_2861116 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73127 RMVar_ID_73127 Human_SNP_ID_591390515 m1A Human chr16 + 2766177 2766145 2766178 CACCGGCGATCCAGGTCCAGAACCCCCCTGATAAGCCGACGTAGGTCCAGATCTCGAACTTCACC C_________________________________GCCGACGTAGGTCCAGATCTCGAACTTCACC CACCGGCGATCCAGGTCCAGAACCCCCCTGATAA C SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2766076..2766264 26863410 MeRIP-seq:(Medium) rs1168306166 Functional Loss DEL dbSNP153 2..34 33 - - - Human_RBP_ID_45339,Human_RBP_ID_1003757,Human_RBP_ID_1515654,Human_RBP_ID_1840782,Human_RBP_ID_3493720,Human_RBP_ID_6505546,Human_RBP_ID_8431171,Human_RBP_ID_8806494,Human_RBP_ID_12709741,Human_RBP_ID_17253719,Human_RBP_ID_17369371,Human_RBP_ID_17485916,Human_RBP_ID_18676607,Human_RBP_ID_27657837 Human_miRNA_ID_2525468 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73128 RMVar_ID_73128 Human_SNP_ID_591390520 m1A Human chr16 + 2766153 2766153 2766153 AGATCTCGAGCCTCTCCAGCCACTCACCGGCGATCCAGGTCCAGAACCCCCCTGATAAGCCGACG AGATCTCGAGCCTCTCCAGCCACTCACCGGCGGTCCAGGTCCAGAACCCCCCTGATAAGCCGACG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2765405..2766380 26863196 MeRIP-seq:(Medium) rs148417227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45339,Human_RBP_ID_1177602,Human_RBP_ID_1515654,Human_RBP_ID_1840782,Human_RBP_ID_8431171,Human_RBP_ID_8806494,Human_RBP_ID_12709741,Human_RBP_ID_17253719,Human_RBP_ID_17369370,Human_RBP_ID_17485915,Human_RBP_ID_18676607,Human_RBP_ID_27440838 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73129 RMVar_ID_73129 Human_SNP_ID_591390536 m1A Human chr16 + 2766177 2766177 2766177 CACCGGCGATCCAGGTCCAGAACCCCCCTGATAAGCCGACGTAGGTCCAGATCTCGAACTTCACC CACCGGCGATCCAGGTCCAGAACCCCCCTGATGAGCCGACGTAGGTCCAGATCTCGAACTTCACC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2766076..2766264 26863410 MeRIP-seq:(Medium) rs1483213774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45339,Human_RBP_ID_1003757,Human_RBP_ID_1515654,Human_RBP_ID_1840782,Human_RBP_ID_3493720,Human_RBP_ID_6505546,Human_RBP_ID_8431171,Human_RBP_ID_8806494,Human_RBP_ID_12709741,Human_RBP_ID_17253719,Human_RBP_ID_17369371,Human_RBP_ID_17485916,Human_RBP_ID_18676607,Human_RBP_ID_27657837 Human_miRNA_ID_2525468 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73130 RMVar_ID_73130 Human_SNP_ID_591390607 m1A Human chr16 + 2766306 2766306 2766306 TCCCCAGTGAGCAGAAGGCGATCCAGATCCAGAACGCCACCAGTAACCCGCCGTCGTTCAAGGTC TCCCCAGTGAGCAGAAGGCGATCCAGATCCAGGACGCCACCAGTAACCCGCCGTCGTTCAAGGTC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2766256..2766356 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_45339,Human_RBP_ID_277861,Human_RBP_ID_1515654,Human_RBP_ID_1840782,Human_RBP_ID_3493725,Human_RBP_ID_5524019,Human_RBP_ID_6505568,Human_RBP_ID_8431179,Human_RBP_ID_8806501,Human_RBP_ID_12709754,Human_RBP_ID_17369373,Human_RBP_ID_18676617,Human_RBP_ID_27440845 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651,RMVar_hsa_circ_175818 73131 RMVar_ID_73131 Human_SNP_ID_591390807 m1A Human chr16 - 2766606 2766606 2766606 AACAGTGGCGTTCGAGATCTAGAGCGGCGCCGAATAGCTGGAGGTGTCCGGGACCTAGAGCGGCG AACAGTGGCGTTCGAGATCTAGAGCGGCGCCGGATAGCTGGAGGTGTCCGGGACCTAGAGCGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2766558..2766647 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 73132 RMVar_ID_73132 Human_SNP_ID_591391031 m1A Human chr16 - 2766971 2766971 2766971 CATCCATCATGGAGCCGCCGGCTTGCTGCAGGACAGACATGGGTGTTCTAGAGCTGCCAAGGGGT CATCCATCATGGAGCCGCCGGCTTGCTGCAGGGCAGACATGGGTGTTCTAGAGCTGCCAAGGGGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2766951..2766975 26863196 MeRIP-seq:(Medium) rs754669784 Functional Loss SNV dbSNP153 33..33 33 - - - 73133 RMVar_ID_73133 Human_SNP_ID_591391287 m1A Human chr16 + 2767518 2767518 2767518 GCTGCAAACTATCCCTCCAGCTCCAGAACACCACAGGCTCCAGCCTCTGCAAACCTGGTGGGTCC GCTGCAAACTATCCCTCCAGCTCCAGAACACCGCAGGCTCCAGCCTCTGCAAACCTGGTGGGTCC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2767468..2767872 26863196 MeRIP-seq:(Medium) rs1299982581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45342,Human_RBP_ID_299796,Human_RBP_ID_471590,Human_RBP_ID_1515718,Human_RBP_ID_1840850,Human_RBP_ID_4360241,Human_RBP_ID_5524028,Human_RBP_ID_6505724,Human_RBP_ID_8431227,Human_RBP_ID_8806559,Human_RBP_ID_9373691,Human_RBP_ID_12710206,Human_RBP_ID_17253750,Human_RBP_ID_17369386,Human_RBP_ID_17485930,Human_RBP_ID_18676681,Human_RBP_ID_20170013,Human_RBP_ID_22199311,Human_RBP_ID_22800617,Human_RBP_ID_23685322,Human_RBP_ID_26941770,Human_RBP_ID_27239751,Human_RBP_ID_27440884 Human_miRNA_ID_604663,Human_miRNA_ID_681121,Human_miRNA_ID_1395159,Human_miRNA_ID_2273420,Human_miRNA_ID_2715401,Human_miRNA_ID_3051380 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73134 RMVar_ID_73134 Human_SNP_ID_591391359 m1A Human chr16 + 2767630 2767630 2767630 CCGCCGCAGCCTTGGCCCCCGCGAGCCTCACCAGTGCTAGGATGGCTCCAGCATTGTCTGGTGCA CCGCCGCAGCCTTGGCCCCCGCGAGCCTCACCGGTGCTAGGATGGCTCCAGCATTGTCTGGTGCA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:2767579..2767853 26863196 MeRIP-seq:(Medium) rs138065295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_471591,Human_RBP_ID_818618,Human_RBP_ID_1003776,Human_RBP_ID_1515725,Human_RBP_ID_1840853,Human_RBP_ID_4398053,Human_RBP_ID_5524029,Human_RBP_ID_8806564,Human_RBP_ID_12710253,Human_RBP_ID_18676684,Human_RBP_ID_20093686,Human_RBP_ID_22052841,Human_RBP_ID_22800620,Human_RBP_ID_27239751,Human_RBP_ID_27440884 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 73135 RMVar_ID_73135 Human_SNP_ID_591391434 m1A Human chr16 - 2767779 2767779 2767779 GAAGGGGAGGGAGCCCGTTCAGAGGTCATCCTAGATTGGCTTGGGGCAGACGGTGGTGTTCTGGA GAAGGGGAGGGAGCCCGTTCAGAGGTCATCCTGGATTGGCTTGGGGCAGACGGTGGTGTTCTGGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2767584..2767893 26863196 MeRIP-seq:(Medium) rs1305695052 Functional Loss SNV dbSNP153 33..33 33 - - - 73136 RMVar_ID_73136 Human_SNP_ID_591391630 m1A Human chr16 - 2768099 2768099 2768099 AGGAGGAACTCCGCCGCTCCTTTGCTGGCTGCAGGGCGGCTAATGCAGAAGGCTGCTGGGCCCCA AGGAGGAACTCCGCCGCTCCTTTGCTGGCTGCCGGGCGGCTAATGCAGAAGGCTGCTGGGCCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2768049..2768195 26863196 MeRIP-seq:(Medium) rs1364370945 Functional Loss SNV dbSNP153 33..33 33 - - - 73137 RMVar_ID_73137 Human_SNP_ID_591391675 m1A Human chr16 - 2768152 2768150 2768153 GGACGACGACGACGATGATGAAGAAGAGGAGGAGCTAGAGGACGACGACGACGAGGAGGAACTCC GGACGACGACGACGATGATGAAGAAGAGGAG___CTAGAGGACGACGACGACGAGGAGGAACTCC GCTC G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2768101..2768200 26863196 MeRIP-seq:(Medium) rs762670589 Functional Loss DEL dbSNP153 32..34 33 - - - 73138 RMVar_ID_73138 Human_SNP_ID_591391677 m1A Human chr16 - 2768152 2768152 2768152 GGACGACGACGACGATGATGAAGAAGAGGAGGAGCTAGAGGACGACGACGACGAGGAGGAACTCC GGACGACGACGACGATGATGAAGAAGAGGAGGTGCTAGAGGACGACGACGACGAGGAGGAACTCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2768101..2768200 26863196 MeRIP-seq:(Medium) rs780671261 Functional Loss SNV dbSNP153 33..33 33 - - - 73139 RMVar_ID_73139 Human_SNP_ID_591392147 m1A Human chr16 + 2769068 2769068 2769068 AGAGGGACGTCCTCCGGAGCCAACCCCAGCCAAACGGAAGAGGCGCTCTAGCAGTTCCAGTTCCA AGAGGGACGTCCTCCGGAGCCAACCCCAGCCAGACGGAAGAGGCGCTCTAGCAGTTCCAGTTCCA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2769020..2769188 26863196 MeRIP-seq:(Medium) rs1290050191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45348,Human_RBP_ID_234074,Human_RBP_ID_471614,Human_RBP_ID_1840891,Human_RBP_ID_3493785,Human_RBP_ID_5184241,Human_RBP_ID_6505820,Human_RBP_ID_12710638,Human_RBP_ID_18676744,Human_RBP_ID_20110644,Human_RBP_ID_23685372 Human_Splice_Rec_1667158,Human_Splice_Rec_1667282,Human_Splice_Rec_1667288,Human_Splice_Rec_1667292,Human_Splice_Rec_1667294,Human_Splice_Rec_1667296 Human_miRNA_ID_974442,Human_miRNA_ID_2443064 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_104970,RMVar_hsa_circ_175820 73140 RMVar_ID_73140 Human_SNP_ID_591392172 m1A Human chr16 + 2769114 2769114 2769114 TCTAGCAGTTCCAGTTCCAGCTCCTCCTCTTCATCTTCCTCCTCCTCCTCCTCCTCCTCTTCTTC TCTAGCAGTTCCAGTTCCAGCTCCTCCTCTTCGTCTTCCTCCTCCTCCTCCTCCTCCTCTTCTTC A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2769063..2769280 26863196 MeRIP-seq:(Medium) rs771504855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4360331,Human_RBP_ID_8431282,Human_RBP_ID_18938680,Human_RBP_ID_20093692,Human_RBP_ID_22199345,Human_RBP_ID_22800646,Human_RBP_ID_22937829,Human_RBP_ID_23685373,Human_RBP_ID_25203165,Human_RBP_ID_26941802,Human_RBP_ID_27239775 Human_miRNA_ID_1384979,Human_miRNA_ID_3078378 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_104970,RMVar_hsa_circ_175820 73141 RMVar_ID_73141 Human_SNP_ID_591392173 m1A Human chr16 + 2769114 2769114 2769114 TCTAGCAGTTCCAGTTCCAGCTCCTCCTCTTCATCTTCCTCCTCCTCCTCCTCCTCCTCTTCTTC TCTAGCAGTTCCAGTTCCAGCTCCTCCTCTTCTTCTTCCTCCTCCTCCTCCTCCTCCTCTTCTTC A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2769063..2769280 26863196 MeRIP-seq:(Medium) rs771504855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4360331,Human_RBP_ID_8431282,Human_RBP_ID_18938680,Human_RBP_ID_20093692,Human_RBP_ID_22199345,Human_RBP_ID_22800646,Human_RBP_ID_22937829,Human_RBP_ID_23685373,Human_RBP_ID_25203165,Human_RBP_ID_26941802,Human_RBP_ID_27239775 Human_miRNA_ID_1384979,Human_miRNA_ID_3078378 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_104970,RMVar_hsa_circ_175820 73142 RMVar_ID_73142 Human_SNP_ID_591392320 m1A Human chr16 - 2769249 2769249 2769249 CGCTCGCCAGGGGGTGGCTTCTTGGGGCTTGCAGGTTTGGGCAAGGCCTGAGGGCCAGGCTTAGC CGCTCGCCAGGGGGTGGCTTCTTGGGGCTTGCCGGTTTGGGCAAGGCCTGAGGGCCAGGCTTAGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2769201..2769250 26863196 MeRIP-seq:(Medium) rs752379428 Functional Loss SNV dbSNP153 33..33 33 - - - 73143 RMVar_ID_73143 Human_SNP_ID_591392481 m1A Human chr16 + 2769598 2769598 2769598 CCTGTTGCTACTGCCAGGGCTCTGGTCTGGCCACCATCATCTTCTCCCGACTCTGTCCACAGCCT CCTGTTGCTACTGCCAGGGCTCTGGTCTGGCCGCCATCATCTTCTCCCGACTCTGTCCACAGCCT A G SRRM2 Ensembl:ENSG00000167978 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2769578..2769664 26863196 MeRIP-seq:(Medium) rs1053098234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1177630,Human_RBP_ID_1515786,Human_RBP_ID_1840898,Human_RBP_ID_2472507,Human_RBP_ID_3493791,Human_RBP_ID_8431298,Human_RBP_ID_12710760,Human_RBP_ID_17077330,Human_RBP_ID_17874663,Human_RBP_ID_20110667,Human_RBP_ID_22054446,Human_RBP_ID_22651573,Human_RBP_ID_23685390,Human_RBP_ID_27440922 RMVar_hsa_circ_101161,RMVar_hsa_circ_175808,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816 73144 RMVar_ID_73144 Human_SNP_ID_591392605 m1A Human chr16 - 2769825 2769823 2769826 AGCACAGGGCATGTGTGGGGGCGGGCAGGAGGAGAACACAGGGCGGGCAAGGCCCGTTGGTGAAG AGCACAGGGCATGTGTGGGGGCGGGCAGGAG___AACACAGGGCGGGCAAGGCCCGTTGGTGAAG TCTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2769801..2769875 26863196 MeRIP-seq:(Medium) rs1490646260 Functional Loss DEL dbSNP153 32..34 33 - - - 73145 RMVar_ID_73145 Human_SNP_ID_591392654 m1A Human chr16 + 2769981 2769981 2769981 AACTCCTCGTTCTGCAAGACTCCGCTCAAAACAGCACCTTCGAGAAGACTGCCCTGCCCCTTCCC AACTCCTCGTTCTGCAAGACTCCGCTCAAAACCGCACCTTCGAGAAGACTGCCCTGCCCCTTCCC A C SRRM2 Ensembl:ENSG00000167978 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2769930..2770101 26863196 MeRIP-seq:(Medium) rs1248389053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515795,Human_RBP_ID_1840904,Human_RBP_ID_3493797,Human_RBP_ID_8431308,Human_RBP_ID_12710818,Human_RBP_ID_18529731,Human_RBP_ID_18676757,Human_RBP_ID_20110710,Human_RBP_ID_22945631,Human_RBP_ID_23114018,Human_RBP_ID_23685399,Human_RBP_ID_25243557,Human_RBP_ID_26941821 RMVar_hsa_circ_101161,RMVar_hsa_circ_175808,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816 73146 RMVar_ID_73146 Human_SNP_ID_591392732 m1A Human chr16 - 2770166 2770166 2770166 CACACCATCCACCGAGTGCCCAGTGGGCAGGCACAGGGTGCAGCGGGGGATGCAAAGATAAAGAC CACACCATCCACCGAGTGCCCAGTGGGCAGGCCCAGGGTGCAGCGGGGGATGCAAAGATAAAGAC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770151..2770175 26863196 MeRIP-seq:(Medium) rs758410088 Functional Loss SNV dbSNP153 33..33 33 - - - 73147 RMVar_ID_73147 Human_SNP_ID_591392750 m1A Human chr16 - 2770241 2770241 2770241 CCTGACCACCAAACCTCACACCACACAGGGCCAGCCTCAGACCCACCTTTGTCCGCTCACTCACC CCTGACCACCAAACCTCACACCACACAGGGCCGGCCTCAGACCCACCTTTGTCCGCTCACTCACC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr16:2770218..2770357;chr16:2769951..2770400 26863196 MeRIP-seq:(Medium) rs1256080676 Functional Loss SNV dbSNP153 33..33 33 - - - 73148 RMVar_ID_73148 Human_SNP_ID_591393146 m1A Human chr16 - 2770859 2770859 2770859 GTGGTGGAATCCCCCAAAGACAATTTATGGAGACCTGCAAGAGAAGATATGGGTCAACAGGGAGT GTGGTGGAATCCCCCAAAGACAATTTATGGAGTCCTGCAAGAGAAGATATGGGTCAACAGGGAGT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2770851..2770875 26863196 MeRIP-seq:(Medium) rs367780118 Functional Loss SNV dbSNP153 33..33 33 - - - 73149 RMVar_ID_73149 Human_SNP_ID_591393155 m1A Human chr16 + 2770890 2770875 2770891 GTCTCCATAAATTGTCTTTGGGGGATTCCACCACACCCAATGCTCTGGAGCCACAAGGAGTGTCC GTCTCCATAAATTGTCTT________________ACCCAATGCTCTGGAGCCACAAGGAGTGTCC TTGGGGGATTCCACCAC T SRRM2 Ensembl:ENSG00000167978 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770876..2770900 26863196 MeRIP-seq:(Medium) rs986898476 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_471630,Human_RBP_ID_1003789,Human_RBP_ID_1177641,Human_RBP_ID_1515814,Human_RBP_ID_1840914,Human_RBP_ID_2472545,Human_RBP_ID_6505918,Human_RBP_ID_8431329,Human_RBP_ID_8806604,Human_RBP_ID_9061595,Human_RBP_ID_12711077,Human_RBP_ID_17369400,Human_RBP_ID_17485953,Human_RBP_ID_17874669,Human_RBP_ID_18162881,Human_RBP_ID_18676781,Human_RBP_ID_20110793,Human_RBP_ID_22497567,Human_RBP_ID_22800675,Human_RBP_ID_24475981,Human_RBP_ID_26941831,Human_RBP_ID_27440929 Human_Splice_Rec_1667164,Human_Splice_Rec_1667302,Human_Splice_Rec_1667308,Human_Splice_Rec_1667312 Human_miRNA_ID_2825612,Human_miRNA_ID_2859583 RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_87133,RMVar_hsa_circ_175821 73150 RMVar_ID_73150 Human_SNP_ID_591393218 m1A Human chr16 - 2770959 2770959 2770959 CATCCAAGGGCTGCCAAGGTTCAAAGGAGAGCAGACAAGGACCCTCCCACGGCTCTGCTGGGGAA CATCCAAGGGCTGCCAAGGTTCAAAGGAGAGCGGACAAGGACCCTCCCACGGCTCTGCTGGGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2770909..2771006 26863196 MeRIP-seq:(Medium) rs374321308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8431331 73151 RMVar_ID_73151 Human_SNP_ID_591393254 m1A Human chr16 - 2771015 2771012 2771015 AGATTAACATTTCACAGGAACAAAGAAAAAAAAAAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG AGATTAACATTTCACAGGAACAAAGAAAAAAA___GGGGAGGGAAAGGGAGCCCTCCATCCAAGG CTTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770976..2771050 26863196 MeRIP-seq:(Medium) rs372487257 Functional Loss DEL dbSNP153 33..35 33 - - - 73152 RMVar_ID_73152 Human_SNP_ID_591393255 m1A Human chr16 - 2771015 2771012 2771015 AGATTAACATTTCACAGGAACAAAGAAAAAAAAAAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG AGATTAACATTTCACAGGAACAAAGAAAAAAA__AGGGGAGGGAAAGGGAGCCCTCCATCCAAGG CTTT CT - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770976..2771050 26863196 MeRIP-seq:(Medium) rs372487257 Functional Loss DEL dbSNP153 33..34 33 - - - 73153 RMVar_ID_73153 Human_SNP_ID_591393256 m1A Human chr16 - 2771015 2771012 2771015 AGATTAACATTTCACAGGAACAAAGAAAAAAAAAAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG AGATTAACATTTCACAGGAACAAAGAAAAAAA_AAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG CTTT CTT - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770976..2771050 26863196 MeRIP-seq:(Medium) rs372487257 Functional Loss DEL dbSNP153 33..33 33 - - - 73154 RMVar_ID_73154 Human_SNP_ID_591393262 m1A Human chr16 - 2771015 2771015 2771015 AGATTAACATTTCACAGGAACAAAGAAAAAAAAAAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG AGATTAACATTTCACAGGAACAAAGAAAAAAAGAAGGGGAGGGAAAGGGAGCCCTCCATCCAAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2770976..2771050 26863196 MeRIP-seq:(Medium) rs770183962 Functional Loss SNV dbSNP153 33..33 33 - - - 73155 RMVar_ID_73155 Human_SNP_ID_591395641 m1A Human chr16 - 2777102 2777102 2777102 CCCCCAGGACGTGTTCCTCATGATCCGGCGCCACAAGACCACCATCTTCACGGACGCCAAGGAGT CCCCCAGGACGTGTTCCTCATGATCCGGCGCCGCAAGACCACCATCTTCACGGACGCCAAGGAGT T C ELOB Ensembl:ENSG00000103363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2777051..2777150 32194978 MeRIP-seq:(Medium) rs1432660890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233489,Human_RBP_ID_471680,Human_RBP_ID_1177657,Human_RBP_ID_1515837,Human_RBP_ID_1840934,Human_RBP_ID_4360450,Human_RBP_ID_5113838 Human_Splice_Rec_1667318,Human_Splice_Rec_1667326,Human_Splice_Rec_1667340 RMVar_hsa_circ_116717,RMVar_hsa_circ_95252,RMVar_hsa_circ_175823,RMVar_hsa_circ_98160,RMVar_hsa_circ_175822,RMVar_hsa_circ_125249,RMVar_hsa_circ_175826,RMVar_hsa_circ_175827 73156 RMVar_ID_73156 Human_SNP_ID_591395651 m1A Human chr16 - 2777126 2777126 2777126 CTTCGTGCTCACGCCGGCCCGCCGCCCCCAGGACGTGTTCCTCATGATCCGGCGCCACAAGACCA CTTCGTGCTCACGCCGGCCCGCCGCCCCCAGGTCGTGTTCCTCATGATCCGGCGCCACAAGACCA T A ELOB Ensembl:ENSG00000103363 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr16:2777051..2777225;chr16:2777076..2777209 26863410 MeRIP-seq:(Medium) rs777426221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233490,Human_RBP_ID_4392783 Human_Splice_Rec_1667318,Human_Splice_Rec_1667326,Human_Splice_Rec_1667340 RMVar_hsa_circ_116717,RMVar_hsa_circ_95252,RMVar_hsa_circ_175823,RMVar_hsa_circ_98160,RMVar_hsa_circ_175822,RMVar_hsa_circ_125249,RMVar_hsa_circ_175826,RMVar_hsa_circ_175827 73157 RMVar_ID_73157 Human_SNP_ID_591408755 m1A Human chr16 + 2817805 2817805 2817805 GGCTCAGCAGTTCCTCTGACCATCCGAGGACCATGCGGCCGACGGGTCATCACGTCGCGCATCGT GGCTCAGCAGTTCCTCTGACCATCCGAGGACCGTGCGGCCGACGGGTCATCACGTCGCGCATCGT A G PRSS21 Ensembl:ENSG00000007038 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2817801..2817900 26863196 MeRIP-seq:(Medium) rs1039227114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888386,Human_RBP_ID_3502473,Human_RBP_ID_3948641,Human_RBP_ID_19075831,Human_RBP_ID_21971855,Human_RBP_ID_22426222,Human_RBP_ID_22473753,Human_RBP_ID_22581839,Human_RBP_ID_22651589,Human_RBP_ID_22944590 Human_Splice_Rec_1667406,Human_Splice_Rec_1667416,Human_Splice_Rec_1667426,Human_Splice_Rec_1667436,Human_Splice_Rec_1667444 RMVar_hsa_circ_90345,RMVar_hsa_circ_126916,RMVar_hsa_circ_175828,RMVar_hsa_circ_175830,RMVar_hsa_circ_110445,RMVar_hsa_circ_175829 73158 RMVar_ID_73158 Human_SNP_ID_591408772 m1A Human chr16 + 2817833 2817826 2817833 GACCATGCGGCCGACGGGTCATCACGTCGCGCATCGTGGGTGGAGAGGACGCCGAACTCGGGCGT GACCATGCGGCCGACGGGTCATCACG_______TCGTGGGTGGAGAGGACGCCGAACTCGGGCGT GTCGCGCA G PRSS21 Ensembl:ENSG00000007038 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:2817151..2817998;chr16:2817151..2817975;chr16:2817166..2817996 26863196 MeRIP-seq:(Medium) rs1451932470 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_43627,Human_RBP_ID_888386,Human_RBP_ID_8941322,Human_RBP_ID_19075831,Human_RBP_ID_22473753,Human_RBP_ID_22581839,Human_RBP_ID_22944590,Human_RBP_ID_26329713 Human_Splice_Rec_1667406,Human_Splice_Rec_1667416,Human_Splice_Rec_1667426,Human_Splice_Rec_1667436,Human_Splice_Rec_1667444 RMVar_hsa_circ_90345,RMVar_hsa_circ_126916,RMVar_hsa_circ_175828,RMVar_hsa_circ_175830,RMVar_hsa_circ_110445,RMVar_hsa_circ_175829 73159 RMVar_ID_73159 Human_SNP_ID_591408777 m1A Human chr16 + 2817833 2817833 2817833 GACCATGCGGCCGACGGGTCATCACGTCGCGCATCGTGGGTGGAGAGGACGCCGAACTCGGGCGT GACCATGCGGCCGACGGGTCATCACGTCGCGCGTCGTGGGTGGAGAGGACGCCGAACTCGGGCGT A G PRSS21 Ensembl:ENSG00000007038 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:2817151..2817998;chr16:2817151..2817975;chr16:2817166..2817996 26863196 MeRIP-seq:(Medium) rs1361783264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43627,Human_RBP_ID_888386,Human_RBP_ID_8941322,Human_RBP_ID_19075831,Human_RBP_ID_22473753,Human_RBP_ID_22581839,Human_RBP_ID_22944590,Human_RBP_ID_26329713 Human_Splice_Rec_1667406,Human_Splice_Rec_1667416,Human_Splice_Rec_1667426,Human_Splice_Rec_1667436,Human_Splice_Rec_1667444 RMVar_hsa_circ_90345,RMVar_hsa_circ_126916,RMVar_hsa_circ_175828,RMVar_hsa_circ_175830,RMVar_hsa_circ_110445,RMVar_hsa_circ_175829 73160 RMVar_ID_73160 Human_SNP_ID_591408840 m1A Human chr16 + 2817940 2817940 2817940 TGCGGAGTGAGCCTGCTCAGCCACCGCTGGGCACTCACGGCGGCGCACTGCTTTGAAACGTGAGT TGCGGAGTGAGCCTGCTCAGCCACCGCTGGGCGCTCACGGCGGCGCACTGCTTTGAAACGTGAGT A G PRSS21 Ensembl:ENSG00000007038 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2817901..2817975 26863196 MeRIP-seq:(Medium) rs1567273329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3948642,Human_RBP_ID_22052857,Human_RBP_ID_22759761,Human_RBP_ID_22944590 Human_Splice_Rec_1667407,Human_Splice_Rec_1667417,Human_Splice_Rec_1667427,Human_Splice_Rec_1667437,Human_Splice_Rec_1667445,Human_Splice_Rec_1667453,Human_Splice_Rec_1667457,Human_Splice_Rec_1667461 RMVar_hsa_circ_90345,RMVar_hsa_circ_126916,RMVar_hsa_circ_175828,RMVar_hsa_circ_175830,RMVar_hsa_circ_110445,RMVar_hsa_circ_175829 73161 RMVar_ID_73161 Human_SNP_ID_591409354 m1A Human chr16 - 2819521 2819521 2819521 CGCCCAGTCTGGGGCTGCCGGGGCTCCTCCGGATGCTGGGCCCACTTCTTTCAGGGCATGTGTGT CGCCCAGTCTGGGGCTGCCGGGGCTCCTCCGGCTGCTGGGCCCACTTCTTTCAGGGCATGTGTGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2819515..2819762 26863196 MeRIP-seq:(Medium) rs949609140 Functional Loss SNV dbSNP153 33..33 33 - - - 73162 RMVar_ID_73162 Human_SNP_ID_591412915 m1A Human chr16 + 2831436 2831436 2831436 TCTGCTTGGAGTGACTAAGGCTCGGGAGGTCCAGGCTCGGCCAGAGGCAGCTCATATGTGGGCCA TCTGCTTGGAGTGACTAAGGCTCGGGAGGTCCGGGCTCGGCCAGAGGCAGCTCATATGTGGGCCA A G ZG16B Ensembl:ENSG00000162078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2831427..2831522 26863196 MeRIP-seq:(Medium) rs558291145 Functional Loss SNV dbSNP153 33..33 33 - - - 73163 RMVar_ID_73163 Human_SNP_ID_591413368 m1A Human chr16 + 2832856 2832856 2832856 TGTGCTTCAGGGAAGTCTTCCTAGAGGAGGCAATGTCTGAGCTAAGTCTTAAAGGATGAAGGACA TGTGCTTCAGGGAAGTCTTCCTAGAGGAGGCAGTGTCTGAGCTAAGTCTTAAAGGATGAAGGACA A G ZG16B Ensembl:ENSG00000162078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2832854..2832937 26863196 MeRIP-seq:(Medium) rs1005101133 Functional Loss SNV dbSNP153 33..33 33 - - - 73164 RMVar_ID_73164 Human_SNP_ID_591413432 m1A Human chr16 + 2833138 2833138 2833138 GGTTTTCAGTCCTTTGGGACCATGATCCACAGAGAGAAATTGATCCTACTTGAGACACAGGAAGC GGTTTTCAGTCCTTTGGGACCATGATCCACAGGGAGAAATTGATCCTACTTGAGACACAGGAAGC A G ZG16B Ensembl:ENSG00000162078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2833131..2833219 26863196 MeRIP-seq:(Medium) rs1051459612 Functional Loss SNV dbSNP153 33..33 33 - - - 73165 RMVar_ID_73165 Human_SNP_ID_591429237 m1A Human chr16 - 2883334 2883334 2883334 CGACGACAGCGGTGCCCTCCCTCTCCGGCGACAGCGCCGCGGCGGGTCCCTCAGCCTCCGCGCCA CGACGACAGCGGTGCCCTCCCTCTCCGGCGACGGCGCCGCGGCGGGTCCCTCAGCCTCCGCGCCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2883251..2895283 26863410 MeRIP-seq:(Medium) rs1423164357 Functional Loss SNV dbSNP153 33..33 33 - - - 73166 RMVar_ID_73166 Human_SNP_ID_591429241 m1A Human chr16 + 2883349 2883349 2883349 GGGACCCGCCGCGGCGCTGTCGCCGGAGAGGGAGGGCACCGCTGTCGTCGGTGAGGACGGGCCCT GGGACCCGCCGCGGCGCTGTCGCCGGAGAGGGCGGGCACCGCTGTCGTCGGTGAGGACGGGCCCT A C FLYWCH2 Ensembl:ENSG00000162076 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2883226..2883442 26863196 MeRIP-seq:(Medium) rs1234851970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392785 Human_Splice_Rec_1667591,Human_Splice_Rec_1667597,Human_Splice_Rec_1667599 RMVar_hsa_circ_81103,RMVar_hsa_circ_175831 73167 RMVar_ID_73167 Human_SNP_ID_591429242 m1A Human chr16 + 2883349 2883349 2883349 GGGACCCGCCGCGGCGCTGTCGCCGGAGAGGGAGGGCACCGCTGTCGTCGGTGAGGACGGGCCCT GGGACCCGCCGCGGCGCTGTCGCCGGAGAGGGTGGGCACCGCTGTCGTCGGTGAGGACGGGCCCT A T FLYWCH2 Ensembl:ENSG00000162076 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2883226..2883442 26863196 MeRIP-seq:(Medium) rs1234851970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392785 Human_Splice_Rec_1667591,Human_Splice_Rec_1667597,Human_Splice_Rec_1667599 RMVar_hsa_circ_81103,RMVar_hsa_circ_175831 73168 RMVar_ID_73168 Human_SNP_ID_591433884 m1A Human chr16 + 2896475 2896475 2896475 TCCCGGGATGCCCCTGCCCGAGCCCAGCGAGCAGGAGGGTGAGAGTGTGAAGGCCAGCCAGGAGC TCCCGGGATGCCCCTGCCCGAGCCCAGCGAGCCGGAGGGTGAGAGTGTGAAGGCCAGCCAGGAGC A C FLYWCH2 Ensembl:ENSG00000162076 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2896426..2896500 26863196 MeRIP-seq:(Medium) rs762626220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761727 RMVar_hsa_circ_81103,RMVar_hsa_circ_175831,RMVar_hsa_circ_175833,RMVar_hsa_circ_34985 73169 RMVar_ID_73169 Human_SNP_ID_591434730 m1A Human chr16 - 2899014 2899014 2899014 GCGAGAGAAGAGGGTGGATCAGGCTGGTGTCAATGGAGATGGGAGGGCTCAGCTTGGCTGTTGGG GCGAGAGAAGAGGGTGGATCAGGCTGGTGTCAGTGGAGATGGGAGGGCTCAGCTTGGCTGTTGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2899011..2899153 26863196 MeRIP-seq:(Medium) rs370800734 Functional Loss SNV dbSNP153 33..33 33 - - - 73170 RMVar_ID_73170 Human_SNP_ID_591434731 m1A Human chr16 - 2899014 2899014 2899014 GCGAGAGAAGAGGGTGGATCAGGCTGGTGTCAATGGAGATGGGAGGGCTCAGCTTGGCTGTTGGG GCGAGAGAAGAGGGTGGATCAGGCTGGTGTCACTGGAGATGGGAGGGCTCAGCTTGGCTGTTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2899011..2899153 26863196 MeRIP-seq:(Medium) rs370800734 Functional Loss SNV dbSNP153 33..33 33 - - - 73171 RMVar_ID_73171 Human_SNP_ID_591434789 m1A Human chr16 - 2899125 2899125 2899125 TGTCAAGGTTACAGGGACTTGCCGGGCGCCACAGAGCAGGGGGCAAAGTTCTCCCCAGCAGCCTC TGTCAAGGTTACAGGGACTTGCCGGGCGCCACGGAGCAGGGGGCAAAGTTCTCCCCAGCAGCCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2898901..2899138 32194978 MeRIP-seq:(Medium) rs1293933415 Functional Loss SNV dbSNP153 33..33 33 - - - 73172 RMVar_ID_73172 Human_SNP_ID_591436658 m1A Human chr16 - 2904922 2904922 2904922 TCCACATCCCCGGCGGTTCCTCTGAAATCCGCACCCCCCAACCCCGGAACCTCGGCTCTTCCGCG TCCACATCCCCGGCGGTTCCTCTGAAATCCGCTCCCCCCAACCCCGGAACCTCGGCTCTTCCGCG T A lnc-PRSS22-5,lnc-PRSS22-5:2,lnc-PRSS22-5:3 RNACentral:URS0000D5BEEB,RNACentral:URS0000D58651,RNACentral:URS0000D59B1B lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2904900..2905024 26863196 MeRIP-seq:(Medium) rs994671816 Functional Loss SNV dbSNP153 33..33 33 - - - 73173 RMVar_ID_73173 Human_SNP_ID_591437108 m1A Human chr16 + 2905836 2905836 2905836 CAAAAGGGCGGGGATGGACCAATGGGCGAGGGATGGGCTGGGCCAATGGGCGTGGCTAGACCAAT CAAAAGGGCGGGGATGGACCAATGGGCGAGGGCTGGGCTGGGCCAATGGGCGTGGCTAGACCAAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2905800..2906174 26863196 MeRIP-seq:(Medium) rs1387373043 Functional Loss SNV dbSNP153 33..33 33 - - - 73174 RMVar_ID_73174 Human_SNP_ID_591445536 m1A Human chr16 + 2929720 2929718 2929720 GCCCCTGCCCGAGCCCAGCGAGCAGGAGGGCGAGAGTGTGAAGGCCGGCCAGGAGCCATCCCCCA GCCCCTGCCCGAGCCCAGCGAGCAGGAGGGC__GAGTGTGAAGGCCGGCCAGGAGCCATCCCCCA CGA C FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2928910..2934666 32194978 MeRIP-seq:(Medium) rs1322049223 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_22370 73175 RMVar_ID_73175 Human_SNP_ID_591445539 m1A Human chr16 + 2929720 2929720 2929720 GCCCCTGCCCGAGCCCAGCGAGCAGGAGGGCGAGAGTGTGAAGGCCGGCCAGGAGCCATCCCCCA GCCCCTGCCCGAGCCCAGCGAGCAGGAGGGCGGGAGTGTGAAGGCCGGCCAGGAGCCATCCCCCA A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2928910..2934666 32194978 MeRIP-seq:(Medium) rs766140140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22370 73176 RMVar_ID_73176 Human_SNP_ID_591445546 m1A Human chr16 + 2929729 2929729 2929729 CGAGCCCAGCGAGCAGGAGGGCGAGAGTGTGAAGGCCGGCCAGGAGCCATCCCCCAAGCCAGGCA CGAGCCCAGCGAGCAGGAGGGCGAGAGTGTGAGGGCCGGCCAGGAGCCATCCCCCAAGCCAGGCA A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:2928860..2930010;chr16:2929618..2929856 26863196 MeRIP-seq:(Medium) rs767588309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22370 73177 RMVar_ID_73177 Human_SNP_ID_591446078 m1A Human chr16 + 2930818 2930818 2930818 GGTGCTGAGCAAGCCGGCCCTGGAGGAGGAGGAGGCACCCCGAGCCCTGTCACTGCTGAGCCTGC GGTGCTGAGCAAGCCGGCCCTGGAGGAGGAGGCGGCACCCCGAGCCCTGTCACTGCTGAGCCTGC A C FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2930770..2930899 26863196 MeRIP-seq:(Medium) rs769636191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1667611,Human_Splice_Rec_1667635,Human_Splice_Rec_1667663 RMVar_hsa_circ_22370 73178 RMVar_ID_73178 Human_SNP_ID_591447266 m1A Human chr16 + 2933250 2933250 2933250 TGTCGGGGACAAGGTGTATTGGACCTGCCGGGACCACGCGCTGCACGGCTGCCGGAGCCGGGCCA TGTCGGGGACAAGGTGTATTGGACCTGCCGGGTCCACGCGCTGCACGGCTGCCGGAGCCGGGCCA A T FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2933201..2933505 26863196 MeRIP-seq:(Medium) rs538130265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234579 73179 RMVar_ID_73179 Human_SNP_ID_591447299 m1A Human chr16 - 2933283 2933283 2933283 CACGCATCACAGTCACCCGCTGTCCCTGGGTGATGGCCCGGCTCCGGCAGCCGTGCAGCGCGTGG CACGCATCACAGTCACCCGCTGTCCCTGGGTGGTGGCCCGGCTCCGGCAGCCGTGCAGCGCGTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2933234..2933550 26863196 MeRIP-seq:(Medium) rs1452586361 Functional Loss SNV dbSNP153 33..33 33 - - - 73180 RMVar_ID_73180 Human_SNP_ID_591447822 m1A Human chr16 + 2933902 2933902 2933902 CCGACGGGTGACTGTCATGCGTGGTCACTGCCACCCGCCCGACCTGGGAGGCCTGGAGGCCCTGA CCGACGGGTGACTGTCATGCGTGGTCACTGCCCCCCGCCCGACCTGGGAGGCCTGGAGGCCCTGA A C FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:2933830..2933931 32194978 MeRIP-seq:(Medium) rs754321432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234580 Human_Splice_Rec_1667615,Human_Splice_Rec_1667639,Human_Splice_Rec_1667667,Human_Splice_Rec_1667675,Human_Splice_Rec_1667687,Human_Splice_Rec_1667693 RMVar_hsa_circ_68478 73181 RMVar_ID_73181 Human_SNP_ID_591447823 m1A Human chr16 + 2933902 2933902 2933902 CCGACGGGTGACTGTCATGCGTGGTCACTGCCACCCGCCCGACCTGGGAGGCCTGGAGGCCCTGA CCGACGGGTGACTGTCATGCGTGGTCACTGCCTCCCGCCCGACCTGGGAGGCCTGGAGGCCCTGA A T FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:2933830..2933931 32194978 MeRIP-seq:(Medium) rs754321432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234580 Human_Splice_Rec_1667615,Human_Splice_Rec_1667639,Human_Splice_Rec_1667667,Human_Splice_Rec_1667675,Human_Splice_Rec_1667687,Human_Splice_Rec_1667693 RMVar_hsa_circ_68478 73182 RMVar_ID_73182 Human_SNP_ID_591447884 m1A Human chr16 + 2933965 2933965 2933965 GAGGCAGCGGGAGAAACGCCCCAACACGGCGCAGCGGGGGAGCCCAGGTACCTGGGGGTGGGCTG GAGGCAGCGGGAGAAACGCCCCAACACGGCGCCGCGGGGGAGCCCAGGTACCTGGGGGTGGGCTG A C FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2933914..2934026 26863196 MeRIP-seq:(Medium) rs1272592847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19073086 Human_Splice_Rec_1667615,Human_Splice_Rec_1667639,Human_Splice_Rec_1667667,Human_Splice_Rec_1667675,Human_Splice_Rec_1667687,Human_Splice_Rec_1667693 RMVar_hsa_circ_68478 73183 RMVar_ID_73183 Human_SNP_ID_591447998 m1A Human chr16 + 2934143 2934143 2934143 TGGCCCTGGCCTCCTACTCCTTGGCCCCCCTGATGCCGCTTTCAATGGGTCTCACCTTCCTGCTC TGGCCCTGGCCTCCTACTCCTTGGCCCCCCTGCTGCCGCTTTCAATGGGTCTCACCTTCCTGCTC A C FLYWCH1 Ensembl:ENSG00000059122 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2934137..2934224 26863196 MeRIP-seq:(Medium) rs1202037409 Functional Loss SNV dbSNP153 33..33 33 - - - 73184 RMVar_ID_73184 Human_SNP_ID_591449345 m1A Human chr16 - 2936770 2936770 2936770 GGGTGCGCCGTGCCTGGTTGGTCAGAGGAATGACCCGGGGCCCTCTGGGGACAAAGCTGCTCAGG GGGTGCGCCGTGCCTGGTTGGTCAGAGGAATGTCCCGGGGCCCTCTGGGGACAAAGCTGCTCAGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2936764..2936915 32194978 MeRIP-seq:(Medium) rs1404075121 Functional Loss SNV dbSNP153 33..33 33 - - - 73185 RMVar_ID_73185 Human_SNP_ID_591461703 m1A Human chr16 + 2967986 2967986 2967986 CGCGGGCTACCGGCCTCTGAGTGCCTCCAGCCAGAGCTCCCTGCGCTCGCTCATCTCCGCTCTCT CGCGGGCTACCGGCCTCTGAGTGCCTCCAGCCGGAGCTCCCTGCGCTCGCTCATCTCCGCTCTCT A G KREMEN2 Ensembl:ENSG00000131650 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2967937..2968055 26863196 MeRIP-seq:(Medium) rs1285366090 Functional Loss SNV dbSNP153 33..33 33 - - - 73186 RMVar_ID_73186 Human_SNP_ID_591462331 m1A Human chr16 + 2969478 2969478 2969478 GCGTCCCCAGCCTCCGCCCCGGCGCGGGGGCGACGGACTCGCGCGTGCGCAGCGCCGGAGGGGCG GCGTCCCCAGCCTCCGCCCCGGCGCGGGGGCGGCGGACTCGCGCGTGCGCAGCGCCGGAGGGGCG A G PAQR4 Ensembl:ENSG00000162073 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:2969379..2969522 26863410 MeRIP-seq:(Medium) rs1031739518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4362880,Human_RBP_ID_5359424,Human_RBP_ID_5419189,Human_RBP_ID_22441232,Human_RBP_ID_22581842 73187 RMVar_ID_73187 Human_SNP_ID_591462388 m1A Human chr16 + 2969629 2969629 2969629 GGCCTTCCCGCGCTGCGGCCCCACTGAGGAGGAGGCTCGGGGACAGCAGGAGCACGGGCTGCCCG GGCCTTCCCGCGCTGCGGCCCCACTGAGGAGGTGGCTCGGGGACAGCAGGAGCACGGGCTGCCCG A T PAQR4 Ensembl:ENSG00000162073 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2969360..2969675 26863196 MeRIP-seq:(Medium) rs1388130564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392789,Human_RBP_ID_5113339,Human_RBP_ID_22441234 73188 RMVar_ID_73188 Human_SNP_ID_591462602 m1A Human chr16 - 2970110 2970110 2970110 CCAGGGCGCTGGGATTACAGAGGCCGGACACCATGCTCCCTACCCCTGGGGCTCAGAGGGATTAA CCAGGGCGCTGGGATTACAGAGGCCGGACACCGTGCTCCCTACCCCTGGGGCTCAGAGGGATTAA T C PKMYT1 Ensembl:ENSG00000127564 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2970105..2970192 26863196 MeRIP-seq:(Medium) rs1304933635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18677473 73189 RMVar_ID_73189 Human_SNP_ID_591463522 m1A Human chr16 - 2972317 2972317 2972317 ACTGGCCACAGGCCTGGTGGGAGGAACAGGATAGGGTGAGGAGGCTCTGGGCTGGCGGCCTGGCA ACTGGCCACAGGCCTGGTGGGAGGAACAGGATCGGGTGAGGAGGCTCTGGGCTGGCGGCCTGGCA T G PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2972267..2972356 26863196 MeRIP-seq:(Medium) rs764876257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261384 RMVar_hsa_circ_175834 73190 RMVar_ID_73190 Human_SNP_ID_591463653 m1A Human chr16 - 2972686 2972686 2972686 ACCCAGCGCTCCTGGCCTTGGGCCAGCAGCTGAAGCCCCATGCTGTGTGGAGCAAAGAGGTTTCC ACCCAGCGCTCCTGGCCTTGGGCCAGCAGCTGCAGCCCCATGCTGTGTGGAGCAAAGAGGTTTCC T G PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2972551..2972725 32194978 MeRIP-seq:(Medium) rs1044636069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1667826,Human_Splice_Rec_1667827 73191 RMVar_ID_73191 Human_SNP_ID_591463740 m1A Human chr16 - 2972926 2972926 2972926 ACCTGAGCCCCAGACTCTGCCTCTGCACTTTTAACCTTTTATCCTGTGTCTCTCCCGTCGCCCTT ACCTGAGCCCCAGACTCTGCCTCTGCACTTTTTACCTTTTATCCTGTGTCTCTCCCGTCGCCCTT T A PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2972876..2973100 26863196 MeRIP-seq:(Medium) rs749253310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004022,Human_RBP_ID_1177753,Human_RBP_ID_1516515,Human_RBP_ID_1841283,Human_RBP_ID_2473027,Human_RBP_ID_3494113,Human_RBP_ID_5495480,Human_RBP_ID_6507567,Human_RBP_ID_8083131,Human_RBP_ID_8432065,Human_RBP_ID_17875254,Human_RBP_ID_18677482,Human_RBP_ID_23273964,Human_RBP_ID_24413112,Human_RBP_ID_24476107,Human_RBP_ID_27441319 Human_miRNA_ID_356835 73192 RMVar_ID_73192 Human_SNP_ID_591463741 m1A Human chr16 + 2972927 2972927 2972927 AGGGCGACGGGAGAGACACAGGATAAAAGGTTAAAAGTGCAGAGGCAGAGTCTGGGGCTCAGGTT AGGGCGACGGGAGAGACACAGGATAAAAGGTTGAAAGTGCAGAGGCAGAGTCTGGGGCTCAGGTT A G PAQR4 Ensembl:ENSG00000162073 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:2972876..2973076 26863196 MeRIP-seq:(Medium) rs1481664581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6507568,Human_RBP_ID_12717094,Human_RBP_ID_22200096,Human_RBP_ID_26444786 73193 RMVar_ID_73193 Human_SNP_ID_591464857 m1A Human chr16 - 2975746 2975746 2975746 TAAAGCGTTCCATGTCACCATTCCGGGGCCCCAAGGACCGGGCCCGCAAGTTGGCCGAGGTGGGC TAAAGCGTTCCATGTCACCATTCCGGGGCCCCGAGGACCGGGCCCGCAAGTTGGCCGAGGTGGGC T C PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2975569..2975825;chr16:2975510..2975826 26863196 MeRIP-seq:(Medium) rs1440227977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113841,Human_RBP_ID_17875272,Human_RBP_ID_18418645,Human_RBP_ID_21972270,Human_RBP_ID_22800988,Human_RBP_ID_22944969,Human_RBP_ID_24476111,Human_RBP_ID_26328046,Human_RBP_ID_26942724 Human_Splice_Rec_1667816,Human_Splice_Rec_1667836,Human_Splice_Rec_1667856,Human_Splice_Rec_1667882,Human_Splice_Rec_1667898,Human_Splice_Rec_1667914,Human_Splice_Rec_1667928,Human_Splice_Rec_1667944,Human_Splice_Rec_1667952,Human_Splice_Rec_1667958,Human_Splice_Rec_1667964 73194 RMVar_ID_73194 Human_SNP_ID_591465259 m1A Human chr16 - 2976894 2976894 2976894 TCTCCCTCAAGAGGCCCAGGGGGCTCAGCCGGAGCCTCCCACCTCCGCCCCCTGCCAAGGGCAGC TCTCCCTCAAGAGGCCCAGGGGGCTCAGCCGGGGCCTCCCACCTCCGCCCCCTGCCAAGGGCAGC T C PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2976846..2977085 26863196 MeRIP-seq:(Medium) rs1297534503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22532760 Human_miRNA_ID_872038 73195 RMVar_ID_73195 Human_SNP_ID_591465269 m1A Human chr16 - 2976909 2976909 2976909 ACGCAGAACCTGGATTCTCCCTCAAGAGGCCCAGGGGGCTCAGCCGGAGCCTCCCACCTCCGCCC ACGCAGAACCTGGATTCTCCCTCAAGAGGCCCGGGGGGCTCAGCCGGAGCCTCCCACCTCCGCCC T C PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2976862..2977088 26863196 MeRIP-seq:(Medium) rs1249754904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234830,Human_RBP_ID_4363082,Human_RBP_ID_17875275,Human_RBP_ID_22532760 73196 RMVar_ID_73196 Human_SNP_ID_591466159 m1A Human chr16 + 2979653 2979653 2979653 TCCCACCGTCCCTGCCCTACGACTTACGTTCTAGCATGACTGGCCTGGCCCAACAGCCTCAGTGG TCCCACCGTCCCTGCCCTACGACTTACGTTCTGGCATGACTGGCCTGGCCCAACAGCCTCAGTGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:2979651..2979700 26863196 MeRIP-seq:(Medium) rs1205106719 Functional Loss SNV dbSNP153 33..33 33 - - - 73197 RMVar_ID_73197 Human_SNP_ID_591466214 m1A Human chr16 + 2979768 2979768 2979768 CTGAGCTAAGGCCAGGCGGGGGTGACCTCCGCAGCTTCCGGGGCCCTGGGCGATCGGGCCGTCTC CTGAGCTAAGGCCAGGCGGGGGTGACCTCCGCGGCTTCCGGGGCCCTGGGCGATCGGGCCGTCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2979719..2979958 26863196 MeRIP-seq:(Medium) rs1272262043 Functional Loss SNV dbSNP153 33..33 33 - - - 73198 RMVar_ID_73198 Human_SNP_ID_591473307 m1A Human chr16 + 3004306 3004306 3004306 CCGCGGCTCGCCCGCGCCCGCGCCCACTCGCGATTGGGCCGGGCCCGCTCGACGCTGCCGCCCAC CCGCGGCTCGCCCGCGCCCGCGCCCACTCGCGGTTGGGCCGGGCCCGCTCGACGCTGCCGCCCAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3004256..3004511 32194978 MeRIP-seq:(Medium) rs1164716415 Functional Loss SNV dbSNP153 33..33 33 - - - 73199 RMVar_ID_73199 Human_SNP_ID_591473334 m1A Human chr16 + 3004365 3004365 3004365 GCCCACCCCGCTGCCCCCGCCGTCCCTGCCGCACCCGCCGTTGCCCGGCCTGCCGCCCGGCCTGA GCCCACCCCGCTGCCCCCGCCGTCCCTGCCGCCCCCGCCGTTGCCCGGCCTGCCGCCCGGCCTGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3004330..3004554 26863196 MeRIP-seq:(Medium) rs1056738025 Functional Loss SNV dbSNP153 33..33 33 - - - 73200 RMVar_ID_73200 Human_SNP_ID_591473474 m1A Human chr16 - 3004681 3004681 3004681 GCGGCGGCGGCTCGGAGACCAGGGGCGGGCGGACGAGCGCGCCCACGGGCCCAGGGGCTGAGGCG GCGGCGGCGGCTCGGAGACCAGGGGCGGGCGGGCGAGCGCGCCCACGGGCCCAGGGGCTGAGGCG T C AC004233.1 Ensembl:ENSG00000262362 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3004653..3004776 26863196 MeRIP-seq:(Medium) rs373438731 Functional Loss SNV dbSNP153 33..33 33 - - - 73201 RMVar_ID_73201 Human_SNP_ID_591473475 m1A Human chr16 - 3004681 3004681 3004681 GCGGCGGCGGCTCGGAGACCAGGGGCGGGCGGACGAGCGCGCCCACGGGCCCAGGGGCTGAGGCG GCGGCGGCGGCTCGGAGACCAGGGGCGGGCGGCCGAGCGCGCCCACGGGCCCAGGGGCTGAGGCG T G AC004233.1 Ensembl:ENSG00000262362 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3004653..3004776 26863196 MeRIP-seq:(Medium) rs373438731 Functional Loss SNV dbSNP153 33..33 33 - - - 73202 RMVar_ID_73202 Human_SNP_ID_591473499 m1A Human chr16 + 3004761 3004761 3004761 TGCCCGCGCGACCCTCTCCCTTCAGCCTGCTGACGGCCCCCGAGACCCGCGACCCATGGCTGCTG TGCCCGCGCGACCCTCTCCCTTCAGCCTGCTGGCGGCCCCCGAGACCCGCGACCCATGGCTGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3004663..3004791 26863196 MeRIP-seq:(Medium) rs1236078 Functional Loss SNV dbSNP153 33..33 33 - - - 73203 RMVar_ID_73203 Human_SNP_ID_591473509 m1A Human chr16 + 3004784 3004784 3004784 AGCCTGCTGACGGCCCCCGAGACCCGCGACCCATGGCTGCTGTCCGCCTTTCCCCTGCCACCGCC AGCCTGCTGACGGCCCCCGAGACCCGCGACCCCTGGCTGCTGTCCGCCTTTCCCCTGCCACCGCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3004741..3004882 32194978 MeRIP-seq:(Medium) rs1376661373 Functional Loss SNV dbSNP153 33..33 33 - - - 73204 RMVar_ID_73204 Human_SNP_ID_591473510 m1A Human chr16 + 3004784 3004784 3004784 AGCCTGCTGACGGCCCCCGAGACCCGCGACCCATGGCTGCTGTCCGCCTTTCCCCTGCCACCGCC AGCCTGCTGACGGCCCCCGAGACCCGCGACCCGTGGCTGCTGTCCGCCTTTCCCCTGCCACCGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3004741..3004882 32194978 MeRIP-seq:(Medium) rs1376661373 Functional Loss SNV dbSNP153 33..33 33 - - - 73205 RMVar_ID_73205 Human_SNP_ID_591479037 m1A Human chr16 - 3020410 3020410 3020410 CAGCACGAGGAGCCGCAGCAACCGGCGCAGCGAGCCCCGAGCCATAGTGCACGTCCTGCGCCCGC CAGCACGAGGAGCCGCAGCAACCGGCGCAGCGCGCCCCGAGCCATAGTGCACGTCCTGCGCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3020351..3020578 26863196 MeRIP-seq:(Medium) rs963788467 Functional Loss SNV dbSNP153 33..33 33 - - - 73206 RMVar_ID_73206 Human_SNP_ID_591479144 m1A Human chr16 - 3020716 3020715 3020716 ATTCGAAGTACTTCGGACTTGTGGAACTGAAGACCCCCCCCAACCCCAATTGGACGGTGGGAGAA ATTCGAAGTACTTCGGACTTGTGGAACTGAAG_CCCCCCCCAACCCCAATTGGACGGTGGGAGAA GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3020707..3020780 26863196 MeRIP-seq:(Medium) rs1567407475 Functional Loss DEL dbSNP153 33..33 33 - - - 73207 RMVar_ID_73207 Human_SNP_ID_591479370 m1A Human chr16 + 3021299 3021299 3021299 CATGGACTGCGCGTCTTGCAGGGCGCGACCGCACAGCGACTTCTGCCTGGGCTGTGAGTGGGGGG CATGGACTGCGCGTCTTGCAGGGCGCGACCGCGCAGCGACTTCTGCCTGGGCTGTGAGTGGGGGG A G TNFRSF12A Ensembl:ENSG00000006327 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3021147..3021450 26863196 MeRIP-seq:(Medium) rs886150208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393546,Human_RBP_ID_22441242,Human_RBP_ID_22760056,Human_RBP_ID_23118571,Human_RBP_ID_27441644 Human_Splice_Rec_1668098,Human_Splice_Rec_1668099,Human_Splice_Rec_1668109,Human_Splice_Rec_1668114,Human_Splice_Rec_1668115,Human_Splice_Rec_1668125 RMVar_hsa_circ_29885 73208 RMVar_ID_73208 Human_SNP_ID_591479785 m1A Human chr16 + 3022350 3022350 3022350 TATTTATTTTGGGGAGAGTTTGGAGGGGAGGGAGAATTTATTAATAAAAGAATCTTTAACTTTAA TATTTATTTTGGGGAGAGTTTGGAGGGGAGGGGGAATTTATTAATAAAAGAATCTTTAACTTTAA A G TNFRSF12A Ensembl:ENSG00000006327 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3022301..3022375 26863196 MeRIP-seq:(Medium) rs1394809873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472934,Human_RBP_ID_6508184,Human_RBP_ID_12719826,Human_RBP_ID_17883661,Human_RBP_ID_27441668 73209 RMVar_ID_73209 Human_SNP_ID_591480129 m1A Human chr16 - 3023290 3023290 3023290 GGCCACCCACTTCTCTCAACTCAGCCTGCACAATGACCACCCCTACTGCAGCCCCCCCATGACCT GGCCACCCACTTCTCTCAACTCAGCCTGCACAGTGACCACCCCTACTGCAGCCCCCCCATGACCT T C HCFC1R1 Ensembl:ENSG00000103145 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3023226..3023540 26863196 MeRIP-seq:(Medium) rs1332488324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113844,Human_RBP_ID_26810965,Human_RBP_ID_27441681 Human_Splice_Rec_1668132,Human_Splice_Rec_1668133,Human_Splice_Rec_1668136,Human_Splice_Rec_1668137,Human_Splice_Rec_1668141,Human_Splice_Rec_1668147,Human_Splice_Rec_1668152,Human_Splice_Rec_1668153,Human_Splice_Rec_1668155,Human_Splice_Rec_1668162,Human_Splice_Rec_1668163,Human_Splice_Rec_1668167,Human_Splice_Rec_1668174,Human_Splice_Rec_1668175 73210 RMVar_ID_73210 Human_SNP_ID_591480442 m1A Human chr16 + 3023983 3023981 3023983 GGGTCCTGCGGGTGGGATCTGGGCGACAGGGGAGGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG GGGTCCTGCGGGTGGGATCTGGGCGACAGGG__GGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG GGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3023951..3024300 26863196 MeRIP-seq:(Medium) rs1433712587 Functional Loss DEL dbSNP153 32..33 33 - - - 73211 RMVar_ID_73211 Human_SNP_ID_591480444 m1A Human chr16 + 3023983 3023983 3023983 GGGTCCTGCGGGTGGGATCTGGGCGACAGGGGAGGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG GGGTCCTGCGGGTGGGATCTGGGCGACAGGGGCGGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3023951..3024300 26863196 MeRIP-seq:(Medium) rs1032873739 Functional Loss SNV dbSNP153 33..33 33 - - - 73212 RMVar_ID_73212 Human_SNP_ID_591480445 m1A Human chr16 + 3023983 3023983 3023983 GGGTCCTGCGGGTGGGATCTGGGCGACAGGGGAGGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG GGGTCCTGCGGGTGGGATCTGGGCGACAGGGGTGGAGTCTCTGAGGGCGTGGCCAAGAGAGGATG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3023951..3024300 26863196 MeRIP-seq:(Medium) rs1032873739 Functional Loss SNV dbSNP153 33..33 33 - - - 73213 RMVar_ID_73213 Human_SNP_ID_591480513 m1A Human chr16 + 3024127 3024127 3024127 GCTCCTCGGGGTGGGGGAGGGTATCCGGCTTAAGGGGGCTGCGGTGGACACCACTTCTTAATGTC GCTCCTCGGGGTGGGGGAGGGTATCCGGCTTATGGGGGCTGCGGTGGACACCACTTCTTAATGTC A T THOC6 Ensembl:ENSG00000131652 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3024045..3024250 26863196 MeRIP-seq:(Medium) rs1156251453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472981,Human_RBP_ID_763668,Human_RBP_ID_3504232,Human_RBP_ID_4393548,Human_RBP_ID_5113845,Human_RBP_ID_5141815,Human_RBP_ID_5316539,Human_RBP_ID_6508319,Human_RBP_ID_8807124,Human_RBP_ID_9325825,Human_RBP_ID_17875621,Human_RBP_ID_22200732,Human_RBP_ID_22497760,Human_RBP_ID_22651605,Human_RBP_ID_26769085,Human_RBP_ID_26780107 73214 RMVar_ID_73214 Human_SNP_ID_591480548 m1A Human chr16 + 3024237 3024237 3024237 TACGCACCAGCCACCTTCGCGCCGAAGGCGGTAGGGCGCCACGGAGAGGAACCGCTCTAGGCACG TACGCACCAGCCACCTTCGCGCCGAAGGCGGTGGGGCGCCACGGAGAGGAACCGCTCTAGGCACG A G THOC6 Ensembl:ENSG00000131652 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3024186..3024286 32194978 MeRIP-seq:(Medium) rs1220013304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393548,Human_RBP_ID_22440840,Human_RBP_ID_27837773 RMVar_hsa_circ_105666,RMVar_hsa_circ_175836 73215 RMVar_ID_73215 Human_SNP_ID_591481518 m1A Human chr16 + 3026750 3026750 3026750 GCACTGCGGGAAAGGAGCCCAGAGGTGCTGTCAGGTGGCGAGGATGGAGCTGTTCGACTTTGGGG GCACTGCGGGAAAGGAGCCCAGAGGTGCTGTCGGGTGGCGAGGATGGAGCTGTTCGACTTTGGGG A G THOC6 Ensembl:ENSG00000131652 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3026676..3026800 32194978 MeRIP-seq:(Medium) rs1447511419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818339,Human_RBP_ID_3948650,Human_RBP_ID_6508474,Human_RBP_ID_17883342 Human_Splice_Rec_1668188,Human_Splice_Rec_1668204,Human_Splice_Rec_1668205,Human_Splice_Rec_1668228,Human_Splice_Rec_1668229,Human_Splice_Rec_1668258,Human_Splice_Rec_1668259,Human_Splice_Rec_1668288,Human_Splice_Rec_1668302,Human_Splice_Rec_1668303 RMVar_hsa_circ_42532,RMVar_hsa_circ_22189,RMVar_hsa_circ_377367,RMVar_hsa_circ_118857,RMVar_hsa_circ_175839 73216 RMVar_ID_73216 Human_SNP_ID_591481877 m1A Human chr16 + 3027499 3027499 3027499 CCTCAACCAGCAGCCTGCCGCGCCTGAGTGCAAGGTGGGTCCGGCAGGGGCCGCGGAGCGGCTGG CCTCAACCAGCAGCCTGCCGCGCCTGAGTGCAGGGTGGGTCCGGCAGGGGCCGCGGAGCGGCTGG A G THOC6 Ensembl:ENSG00000131652 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3027376..3027525 32194978 MeRIP-seq:(Medium) rs761447810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19073114 Human_Splice_Rec_1668213,Human_Splice_Rec_1668237,Human_Splice_Rec_1668267 RMVar_hsa_circ_84777,RMVar_hsa_circ_118857,RMVar_hsa_circ_175839,RMVar_hsa_circ_107529,RMVar_hsa_circ_175840,RMVar_hsa_circ_175841 73217 RMVar_ID_73217 Human_SNP_ID_591492240 m1A Human chr16 + 3057019 3057019 3057019 TCCCCAAGCAGGGGCGGCCGCAGCTCTCACCCACTTTCTCCTGCAGACGGCGAGGGGACCGACCT TCCCCAAGCAGGGGCGGCCGCAGCTCTCACCCTCTTTCTCCTGCAGACGGCGAGGGGACCGACCT A T MMP25 Ensembl:ENSG00000008516 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3057003..3057153 26863196 MeRIP-seq:(Medium) rs1046429448 Functional Loss SNV dbSNP153 33..33 33 - - - 73218 RMVar_ID_73218 Human_SNP_ID_591492575 m1A Human chr16 - 3057600 3057600 3057600 GCCAAGTGAAATGACTCACCTTTGAAGAAGAAAGTTTCCCCTCGGATGTTGGCGATGGCGTCAAA GCCAAGTGAAATGACTCACCTTTGAAGAAGAACGTTTCCCCTCGGATGTTGGCGATGGCGTCAAA T G MMP25-AS1 Ensembl:ENSG00000261971 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3057587..3058424 26863196 MeRIP-seq:(Medium) rs767710690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5097056,Human_RBP_ID_5289685 Human_Splice_Rec_1668461 73219 RMVar_ID_73219 Human_SNP_ID_591493029 m1A Human chr16 - 3058544 3058544 3058544 CCTCGTCGTAGCGCCAGTACTGCCGGCCGCGGACCAGGTAGGTCTTCCCGTTCTGTGGCCACGAG CCTCGTCGTAGCGCCAGTACTGCCGGCCGCGGTCCAGGTAGGTCTTCCCGTTCTGTGGCCACGAG T A MMP25-AS1 Ensembl:ENSG00000261971 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3058530..3058837 26863196 MeRIP-seq:(Medium) rs1567129417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502483,Human_RBP_ID_5465052,Human_RBP_ID_8188671 Human_Splice_Rec_1668457,Human_Splice_Rec_1668465 73220 RMVar_ID_73220 Human_SNP_ID_591493146 m1A Human chr16 + 3058742 3058731 3058742 TGGGGAGAGGGATGTGGGGAATGGGGACATGGAGGCCACCCTGCGGGGATGGGGGTCCTTGGGCA TGGGGAGAGGGATGTGGGGAAT___________GGCCACCCTGCGGGGATGGGGGTCCTTGGGCA TGGGGACATGGA T MMP25 Ensembl:ENSG00000008516 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3058736..3058893 26863196 MeRIP-seq:(Medium) rs1031976307 Functional Loss DEL dbSNP153 23..33 33 - - - 73221 RMVar_ID_73221 Human_SNP_ID_591493174 m1A Human chr16 + 3058800 3058800 3058800 TTGGGCATCAGGGAGCGGCGGGGCGGGGAGGGACCGGGACTCAAGCTCTGCTCCTCCAGGTGACA TTGGGCATCAGGGAGCGGCGGGGCGGGGAGGGGCCGGGACTCAAGCTCTGCTCCTCCAGGTGACA A G MMP25 Ensembl:ENSG00000008516 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3058766..3058944 26863196 MeRIP-seq:(Medium) rs928747045 Functional Loss SNV dbSNP153 33..33 33 - - - 73222 RMVar_ID_73222 Human_SNP_ID_591493448 m1A Human chr16 + 3059270 3059270 3059270 GGATCTCCCGCGCAGGGGCGGCGGCGGCGGGGACCGGTCGCCTGGCGCTGGGCTCAGTCTCCTCA GGATCTCCCGCGCAGGGGCGGCGGCGGCGGGGGCCGGTCGCCTGGCGCTGGGCTCAGTCTCCTCA A G MMP25 Ensembl:ENSG00000008516 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3059169..3059309 26863196 MeRIP-seq:(Medium) rs945269461 Functional Loss SNV dbSNP153 33..33 33 - - - 73223 RMVar_ID_73223 Human_SNP_ID_591498098 m1A Human chr16 - 3069276 3069276 3069276 CCTTGTCCCCCCGTGGGGCTCCGTAGGACTGGAAAGAGGACATGAAGAGCTCTGACAGAGAGCAG CCTTGTCCCCCCGTGGGGCTCCGTAGGACTGGGAAGAGGACATGAAGAGCTCTGACAGAGAGCAG T C MMP25-AS1,lnc-ZSCAN10-5,MMP25-AS1:2 RNACentral:URS0000D5DBB7,RNACentral:URS00008C07B2,RNACentral:URS00008B8F60 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3069194..3069343 32194978 MeRIP-seq:(Medium) rs768143359 Functional Loss SNV dbSNP153 33..33 33 - - - 73224 RMVar_ID_73224 Human_SNP_ID_591498099 m1A Human chr16 - 3069276 3069276 3069276 CCTTGTCCCCCCGTGGGGCTCCGTAGGACTGGAAAGAGGACATGAAGAGCTCTGACAGAGAGCAG CCTTGTCCCCCCGTGGGGCTCCGTAGGACTGGCAAGAGGACATGAAGAGCTCTGACAGAGAGCAG T G MMP25-AS1,lnc-ZSCAN10-5,MMP25-AS1:2 RNACentral:URS0000D5DBB7,RNACentral:URS00008C07B2,RNACentral:URS00008B8F60 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3069194..3069343 32194978 MeRIP-seq:(Medium) rs768143359 Functional Loss SNV dbSNP153 33..33 33 - - - 73225 RMVar_ID_73225 Human_SNP_ID_591498248 m1A Human chr16 - 3069489 3069489 3069489 AGCAGGTTTTATTAAGATGCCAGGGCGACAGCACCAGGTCAGAGCTGCGGCAGGAACGCCAGGCA AGCAGGTTTTATTAAGATGCCAGGGCGACAGCGCCAGGTCAGAGCTGCGGCAGGAACGCCAGGCA T C MMP25-AS1,lnc-ZSCAN10-5,MMP25-AS1:2 RNACentral:URS0000D5DBB7,RNACentral:URS00008C07B2,RNACentral:URS00008B8F60 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3069440..3069540 32194978 MeRIP-seq:(Medium) rs12449264 Functional Loss SNV dbSNP153 33..33 33 - - - 73226 RMVar_ID_73226 Human_SNP_ID_591512656 m1A Human chr16 + 3113262 3113262 3113262 ATAGGATCTGGGAGACTTTCTTTCCGATTGGGACCAGGGAGCGCTGGTACTCGTGGGGATTTTCA ATAGGATCTGGGAGACTTTCTTTCCGATTGGGGCCAGGGAGCGCTGGTACTCGTGGGGATTTTCA A G ZNF205 Ensembl:ENSG00000122386 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3113260..3113438 26863196 MeRIP-seq:(Medium) rs1021155899 Functional Loss SNV dbSNP153 33..33 33 - - - 73227 RMVar_ID_73227 Human_SNP_ID_591514740 m1A Human chr16 + 3119418 3119418 3119418 CCGGAGCTCAGGGCCGGCCAAAGACTCCGGGCAGCCGGCTGAGCCAGATCGCACCCCGGATGCAG CCGGAGCTCAGGGCCGGCCAAAGACTCCGGGCCGCCGGCTGAGCCAGATCGCACCCCGGATGCAG A C ZNF205 Ensembl:ENSG00000122386 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3119370..3119635 26863196 MeRIP-seq:(Medium) rs1292381093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83505,RMVar_hsa_circ_175843 73228 RMVar_ID_73228 Human_SNP_ID_591514793 m1A Human chr16 + 3119511 3119509 3119512 CCAGGAGTACCGCGTCCCGGAGAAGCCCAACGAGGAGGAGAAGGGCGCCCCGGAGAGTGGCGAGG CCAGGAGTACCGCGTCCCGGAGAAGCCCAAC___GAGGAGAAGGGCGCCCCGGAGAGTGGCGAGG CGAG C ZNF205 Ensembl:ENSG00000122386 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3118951..3119601 26863196 MeRIP-seq:(Medium) rs369182482 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_83505,RMVar_hsa_circ_175843 73229 RMVar_ID_73229 Human_SNP_ID_591514962 m1A Human chr16 + 3119824 3119824 3119824 ACGCTGATTCAGCACCAGCGCATCCACACCGGAGAGAAGCCCTACGTGTGCGACCGCTGCGCCAA ACGCTGATTCAGCACCAGCGCATCCACACCGGGGAGAAGCCCTACGTGTGCGACCGCTGCGCCAA A G ZNF205 Ensembl:ENSG00000122386 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3119773..3120170 32194978 MeRIP-seq:(Medium) rs1443921125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3118443 RMVar_hsa_circ_83505,RMVar_hsa_circ_175843 73230 RMVar_ID_73230 Human_SNP_ID_591515279 m1A Human chr16 - 3120439 3120439 3120439 CCTCGCCCTCCCCCATCGCCATGCCTCACCCCATGCCCTCACCGCCCCAGCTCCCTTCCCGAGCC CCTCGCCCTCCCCCATCGCCATGCCTCACCCCGTGCCCTCACCGCCCCAGCTCCCTTCCCGAGCC T C ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3120256..3120484 26863196 MeRIP-seq:(Medium) rs1174396355 Functional Loss SNV dbSNP153 33..33 33 - - - 73231 RMVar_ID_73231 Human_SNP_ID_591521756 m1A Human chr16 + 3140791 3140791 3140791 AGGCAGCGACGTGACTGTGTCCTGGAGCCCCGAGGAGGCTGAGGCCTGGGAGAGCGAGAACCGGC AGGCAGCGACGTGACTGTGTCCTGGAGCCCCGCGGAGGCTGAGGCCTGGGAGAGCGAGAACCGGC A C ZNF213 Ensembl:ENSG00000085644 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3140753..3140833 26863196 MeRIP-seq:(Medium) rs1306252746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27442281 Human_miRNA_ID_341013 73232 RMVar_ID_73232 Human_SNP_ID_591522310 m1A Human chr16 + 3142179 3142179 3142179 ACCTCACTCCATCAGCACTAGCACCTCACTCCATCGGCCCCGGCACCCTGCTCCATCGGCACTGG ACCTCACTCCATCAGCACTAGCACCTCACTCCGTCGGCCCCGGCACCCTGCTCCATCGGCACTGG A G ZNF213 Ensembl:ENSG00000085644 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3142128..3142267 26863196 MeRIP-seq:(Medium) rs1236382282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371625,Human_RBP_ID_27442289 73233 RMVar_ID_73233 Human_SNP_ID_591522473 m1A Human chr16 - 3142492 3142492 3142492 GGAGCAGGGTGGTAGTGCCGACGGAGCTGGACATAGTGATGATGGAGCGGGGTGGTAGTGCCGAT GGAGCAGGGTGGTAGTGCCGACGGAGCTGGACGTAGTGATGATGGAGCGGGGTGGTAGTGCCGAT T C ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3142442..3142603 26863196 MeRIP-seq:(Medium) rs372275666 Functional Loss SNV dbSNP153 33..33 33 - - - 73234 RMVar_ID_73234 Human_SNP_ID_591522544 m1A Human chr16 + 3142621 3142621 3142621 CACCGGCACCAGTGCCTCGCTCCATTGGCACCAACGCCCAGCTCCACCGGTACTGGCTCCCTGCT CACCGGCACCAGTGCCTCGCTCCATTGGCACCGACGCCCAGCTCCACCGGTACTGGCTCCCTGCT A G ZNF213 Ensembl:ENSG00000085644 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3142570..3142652 26863196 MeRIP-seq:(Medium) rs1176882441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371627 73235 RMVar_ID_73235 Human_SNP_ID_591525232 m1A Human chr16 + 3150731 3150731 3150731 GTCTGATTCCGGATCAGAAGATTGAGGGTTCGAGTCCCTTCGTGGTCGTTGCCATGTTAACGTTT GTCTGATTCCGGATCAGAAGATTGAGGGTTCGGGTCCCTTCGTGGTCGTTGCCATGTTAACGTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs946019037 Functional Loss SNV dbSNP153 33..33 33 - - - 73236 RMVar_ID_73236 Human_SNP_ID_591526257 m1A Human chr16 + 3152957 3152957 3152957 ATTGGCCTCCTAAGCCAGGGATTGTGGGTTCGAGTCCCACCCGGGGTAAAGAAAGGCCGAATTTT ATTGGCCTCCTAAGCCAGGGATTGTGGGTTCGGGTCCCACCCGGGGTAAAGAAAGGCCGAATTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1214974853 Functional Loss SNV dbSNP153 33..33 33 - - - 73237 RMVar_ID_73237 Human_SNP_ID_591526427 m1A Human chr16 + 3153077 3153070 3153077 GAGTTTCCGAAGGGTTACCAAAAAGGCTCTAAATCAGAAACCTCTACCTGTTTTCAAGGAAGACG GAGTTTCCGAAGGGTTACCAAAAAGG_______TCAGAAACCTCTACCTGTTTTCAAGGAAGACG GCTCTAAA G lnc-ZNF213-3 RNACentral:URS0000D588F3 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:3152981..3153108 26863410 MeRIP-seq:(Medium) rs1051983623 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_6510692,Human_RBP_ID_20117755,Human_RBP_ID_23128203 73238 RMVar_ID_73238 Human_SNP_ID_591526436 m1A Human chr16 + 3153077 3153077 3153077 GAGTTTCCGAAGGGTTACCAAAAAGGCTCTAAATCAGAAACCTCTACCTGTTTTCAAGGAAGACG GAGTTTCCGAAGGGTTACCAAAAAGGCTCTAAGTCAGAAACCTCTACCTGTTTTCAAGGAAGACG A G lnc-ZNF213-3 RNACentral:URS0000D588F3 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:3152981..3153108 26863410 MeRIP-seq:(Medium) rs1171474845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6510692,Human_RBP_ID_20117755,Human_RBP_ID_23128203 73239 RMVar_ID_73239 Human_SNP_ID_591526458 m1A Human chr16 - 3153095 3153095 3153095 GTAACGTGAAATTGTGCTCGTCTTCCTTGAAAACAGGTAGAGGTTTCTGATTTAGAGCCTTTTTG GTAACGTGAAATTGTGCTCGTCTTCCTTGAAAGCAGGTAGAGGTTTCTGATTTAGAGCCTTTTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3152979..3153104 26863196 MeRIP-seq:(Medium) rs1373820439 Functional Loss SNV dbSNP153 33..33 33 - - - 73240 RMVar_ID_73240 Human_SNP_ID_591528071 m1A Human chr16 - 3157420 3157420 3157420 ATGAGACCCTTAATCTCAGGGTCGTGGGTTCGAGCCCCACGTTGGGCGTGAGATTTTGTCGGATG ATGAGACCCTTAATCTCAGGGTCGTGGGTTCGGGCCCCACGTTGGGCGTGAGATTTTGTCGGATG T C AC108134.2 Ensembl:ENSG00000261889 lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1198971498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234460,Human_RBP_ID_277485,Human_RBP_ID_473587,Human_RBP_ID_762666,Human_RBP_ID_1004337,Human_RBP_ID_1131201,Human_RBP_ID_1238059,Human_RBP_ID_1517867,Human_RBP_ID_1842035,Human_RBP_ID_3494691,Human_RBP_ID_4395409,Human_RBP_ID_5088103,Human_RBP_ID_5184040,Human_RBP_ID_5259223,Human_RBP_ID_6510693,Human_RBP_ID_8188673,Human_RBP_ID_8252115,Human_RBP_ID_8433099,Human_RBP_ID_8807481,Human_RBP_ID_12727958,Human_RBP_ID_17079360,Human_RBP_ID_17690219,Human_RBP_ID_17876251,Human_RBP_ID_18207573,Human_RBP_ID_18545385,Human_RBP_ID_18678725,Human_RBP_ID_20093819,Human_RBP_ID_22004153,Human_RBP_ID_22497851,Human_RBP_ID_22801476,Human_RBP_ID_23128212,Human_RBP_ID_23688031,Human_RBP_ID_26757151,Human_RBP_ID_26944431,Human_RBP_ID_27241580,Human_RBP_ID_27658217 73241 RMVar_ID_73241 Human_SNP_ID_591528947 m1A Human chr16 + 3158977 3158965 3158978 TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGCTTTTTTTTTTTTTT TTCTCGCTTTGGGTGCGAGAG_____________ATCCCGGACGAGCCCGCTTTTTTTTTTTTTT GGTCCCGGGTTCAA G tRNA-Pro-TGG-3-2 RNACentral:URS00002D40C8 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1214355423 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_1517873,Human_RBP_ID_5274650,Human_RBP_ID_8252117,Human_RBP_ID_8433103,Human_RBP_ID_22801477,Human_RBP_ID_23128221 73242 RMVar_ID_73242 Human_SNP_ID_591536752 m1A Human chr16 - 3180569 3180569 3180569 ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGAGCCGCACGTTGGGCGTGCCTTTTGCTGTACCA ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGGGCCGCACGTTGGGCGTGCCTTTTGCTGTACCA T C tRNA-Lys-CTT-5-1,TRK-CTT5-1 RNACentral:URS00006C0A49,RNACentral:URS0000001346 tRNA,tRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1374769963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1517885,Human_RBP_ID_1842036,Human_RBP_ID_5184192,Human_RBP_ID_5259231,Human_RBP_ID_8433112,Human_RBP_ID_9062014,Human_RBP_ID_18678738,Human_RBP_ID_20117775,Human_RBP_ID_23128248,Human_RBP_ID_24413167,Human_RBP_ID_24476244,Human_RBP_ID_27241589 73243 RMVar_ID_73243 Human_SNP_ID_591536807 m1A Human chr16 - 3180608 3180608 3180608 GATCCTATAAGGAAGCCCGGCTAGCTCAGTCGATAGAGCATGAGACTCTTAATCTCAGGGTCGTG GATCCTATAAGGAAGCCCGGCTAGCTCAGTCGGTAGAGCATGAGACTCTTAATCTCAGGGTCGTG T C tRNA-Lys-CTT-5-1,TRK-CTT5-1 RNACentral:URS00006C0A49,RNACentral:URS0000001346 tRNA,tRNA intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs938248327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473593,Human_RBP_ID_1177982,Human_RBP_ID_1517889,Human_RBP_ID_4395652,Human_RBP_ID_5259232,Human_RBP_ID_6510708,Human_RBP_ID_8433113,Human_RBP_ID_9062014,Human_RBP_ID_12727982,Human_RBP_ID_17876260,Human_RBP_ID_18530323,Human_RBP_ID_18678738,Human_RBP_ID_23128248,Human_RBP_ID_23688040 73244 RMVar_ID_73244 Human_SNP_ID_591537487 m1A Human chr16 - 3182597 3182597 3182597 TTGGTCCAAAATATCGGTTTCTACCCTTTCCTACTTTAGATGAAGATCAGAGATCCAGACAGCTC TTGGTCCAAAATATCGGTTTCTACCCTTTCCTTCTTTAGATGAAGATCAGAGATCCAGACAGCTC T A AJ003147.1 Ensembl:ENSG00000262521 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3182551..3182635 26863196 MeRIP-seq:(Medium) rs1389302813 Functional Loss SNV dbSNP153 33..33 33 - - - 73245 RMVar_ID_73245 Human_SNP_ID_591537548 m1A Human chr16 - 3182650 3182648 3182651 TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGGTTTTTGGTCCAAAAT TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTC___TCCCGGACGAGCCCGGTTTTTGGTCCAAAAT ATTT A AJ003147.1 Ensembl:ENSG00000262521 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1247771371 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_125789,Human_RBP_ID_473595,Human_RBP_ID_1517891,Human_RBP_ID_4395585,Human_RBP_ID_5259235,Human_RBP_ID_5465083,Human_RBP_ID_8252123,Human_RBP_ID_8433115,Human_RBP_ID_17121416,Human_RBP_ID_17883343,Human_RBP_ID_18486239,Human_RBP_ID_18545389,Human_RBP_ID_21888722,Human_RBP_ID_23128255,Human_RBP_ID_23688042,Human_RBP_ID_27838179 73246 RMVar_ID_73246 Human_SNP_ID_591537551 m1A Human chr16 - 3182650 3182650 3182650 TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGGTTTTTGGTCCAAAAT TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCATATCCCGGACGAGCCCGGTTTTTGGTCCAAAAT T A AJ003147.1 Ensembl:ENSG00000262521 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1282359083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125789,Human_RBP_ID_473595,Human_RBP_ID_1517891,Human_RBP_ID_4395585,Human_RBP_ID_5259235,Human_RBP_ID_5465083,Human_RBP_ID_8252123,Human_RBP_ID_8433115,Human_RBP_ID_17121416,Human_RBP_ID_17883343,Human_RBP_ID_18486239,Human_RBP_ID_18545389,Human_RBP_ID_21888722,Human_RBP_ID_23128255,Human_RBP_ID_23688042,Human_RBP_ID_27838179 73247 RMVar_ID_73247 Human_SNP_ID_591537676 m1A Human chr16 - 3182746 3182746 3182746 GCTGGGTCCCCACCTCTGGCCACGAGGACTCCACGAAGGCCACAAAGACAAGCCGGAGGCTACGG GCTGGGTCCCCACCTCTGGCCACGAGGACTCCTCGAAGGCCACAAAGACAAGCCGGAGGCTACGG T A AJ003147.1 Ensembl:ENSG00000262521 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3182695..3182819 26863196 MeRIP-seq:(Medium) rs1233421931 Functional Loss SNV dbSNP153 33..33 33 - - - 73248 RMVar_ID_73248 Human_SNP_ID_591540298 m1A Human chr16 + 3189689 3189689 3189689 TTCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGGCTTTTGGTGCAGGG TTCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCCAATCCCGGACGAGCCCGGCTTTTGGTGCAGGG A C AJ003147.2 Ensembl:ENSG00000262668 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1378770875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125792,Human_RBP_ID_277488,Human_RBP_ID_1527434,Human_RBP_ID_5259711,Human_RBP_ID_8252125,Human_RBP_ID_8433117,Human_RBP_ID_12727989,Human_RBP_ID_17121419,Human_RBP_ID_17690222,Human_RBP_ID_17876263,Human_RBP_ID_18545395,Human_RBP_ID_18678744,Human_RBP_ID_21888723,Human_RBP_ID_22802967,Human_RBP_ID_23128265,Human_RBP_ID_23688048,Human_RBP_ID_26944440,Human_RBP_ID_27838180 73249 RMVar_ID_73249 Human_SNP_ID_591540299 m1A Human chr16 + 3189689 3189689 3189689 TTCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGGCTTTTGGTGCAGGG TTCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCGAATCCCGGACGAGCCCGGCTTTTGGTGCAGGG A G AJ003147.2 Ensembl:ENSG00000262668 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1378770875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125792,Human_RBP_ID_277488,Human_RBP_ID_1527434,Human_RBP_ID_5259711,Human_RBP_ID_8252125,Human_RBP_ID_8433117,Human_RBP_ID_12727989,Human_RBP_ID_17121419,Human_RBP_ID_17690222,Human_RBP_ID_17876263,Human_RBP_ID_18545395,Human_RBP_ID_18678744,Human_RBP_ID_21888723,Human_RBP_ID_22802967,Human_RBP_ID_23128265,Human_RBP_ID_23688048,Human_RBP_ID_26944440,Human_RBP_ID_27838180 73250 RMVar_ID_73250 Human_SNP_ID_591541325 m1A Human chr16 + 3192044 3192044 3192044 TTCTCGCTTAGGATGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCCTCTTCTTATTTTTGA TTCTCGCTTAGGATGCGAGAGGTCCCGGGTTCCAATCCCGGACGAGCCCCTCTTCTTATTTTTGA A C AJ003147.2 Ensembl:ENSG00000262668 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1327620285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125795,Human_RBP_ID_1281954,Human_RBP_ID_1517900,Human_RBP_ID_4395588,Human_RBP_ID_5088109,Human_RBP_ID_5180689,Human_RBP_ID_5274656,Human_RBP_ID_5289690,Human_RBP_ID_8252129,Human_RBP_ID_8433121,Human_RBP_ID_9825476,Human_RBP_ID_12727993,Human_RBP_ID_17883994,Human_RBP_ID_18545400,Human_RBP_ID_18678751,Human_RBP_ID_20117789,Human_RBP_ID_21889069,Human_RBP_ID_22370094,Human_RBP_ID_22801488,Human_RBP_ID_23128276,Human_RBP_ID_25208006,Human_RBP_ID_26768864,Human_RBP_ID_26781075,Human_RBP_ID_26944445 73251 RMVar_ID_73251 Human_SNP_ID_591556839 m1A Human chr16 - 3234875 3234875 3234875 GCCGGGTAGGGAGCCTGGTGAGCGCCTCAGGCAGGGGCGCACGCTGAGCTTTACGGTAAAGGTGT GCCGGGTAGGGAGCCTGGTGAGCGCCTCAGGCCGGGGCGCACGCTGAGCTTTACGGTAAAGGTGT T G ZNF200 Ensembl:ENSG00000010539 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3234825..3235129 26863196 MeRIP-seq:(Medium) rs1045414749 Functional Loss SNV dbSNP153 33..33 33 - - - 73252 RMVar_ID_73252 Human_SNP_ID_591573035 m1A Human chr16 + 3283551 3283549 3283551 GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTCTATATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTC__TATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG CTA C ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3283457..3283558 32194978 MeRIP-seq:(Medium) rs76789966 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4367593,Human_RBP_ID_5495617 73253 RMVar_ID_73253 Human_SNP_ID_591573038 m1A Human chr16 + 3283551 3283551 3283551 GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTCTATATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTCTCTATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG A C ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3283457..3283558 32194978 MeRIP-seq:(Medium) rs201726814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4367593,Human_RBP_ID_5495617 73254 RMVar_ID_73254 Human_SNP_ID_591573039 m1A Human chr16 + 3283551 3283551 3283551 GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTCTATATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG GAGCAGAGGTCTGAGTCTTGCGTGGGTCCTCTTTATAGGGTGAGAAGCGTGGCGCTCGGTTCCTG A T ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3283457..3283558 32194978 MeRIP-seq:(Medium) rs201726814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4367593,Human_RBP_ID_5495617 73255 RMVar_ID_73255 Human_SNP_ID_591573046 m1A Human chr16 - 3283559 3283559 3283559 CCCCGAGGCAGGAACCGAGCGCCACGCTTCTCACCCTATATAGAGGACCCACGCAAGACTCAGAC CCCCGAGGCAGGAACCGAGCGCCACGCTTCTCGCCCTATATAGAGGACCCACGCAAGACTCAGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3283511..3283610 26863196 MeRIP-seq:(Medium) rs1470258559 Functional Loss SNV dbSNP153 33..33 33 - - - 73256 RMVar_ID_73256 Human_SNP_ID_591573051 m1A Human chr16 - 3283568 3283568 3283568 CCAGGACTTCCCCGAGGCAGGAACCGAGCGCCACGCTTCTCACCCTATATAGAGGACCCACGCAA CCAGGACTTCCCCGAGGCAGGAACCGAGCGCCTCGCTTCTCACCCTATATAGAGGACCCACGCAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3283517..3283739 26863196 MeRIP-seq:(Medium) rs3826245 Functional Loss SNV dbSNP153 33..33 33 - - - 73257 RMVar_ID_73257 Human_SNP_ID_591573161 m1A Human chr16 + 3283841 3283841 3283841 AGACCTGACGATGGCGTCGGGCCCGGGCTCCCAGGAACGGGAAGGGCTCCTGATAGTGAAGCTGG AGACCTGACGATGGCGTCGGGCCCGGGCTCCCGGGAACGGGAAGGGCTCCTGATAGTGAAGCTGG A G ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3283792..3283999 26863196 MeRIP-seq:(Medium) rs752811374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9286074 73258 RMVar_ID_73258 Human_SNP_ID_591573162 m1A Human chr16 + 3283841 3283841 3283841 AGACCTGACGATGGCGTCGGGCCCGGGCTCCCAGGAACGGGAAGGGCTCCTGATAGTGAAGCTGG AGACCTGACGATGGCGTCGGGCCCGGGCTCCCTGGAACGGGAAGGGCTCCTGATAGTGAAGCTGG A T ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3283792..3283999 26863196 MeRIP-seq:(Medium) rs752811374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9286074 73259 RMVar_ID_73259 Human_SNP_ID_591573790 m1A Human chr16 + 3285753 3285753 3285753 GAACATGGAAGACAAGGAGATGACTGGGCCCCAGGTGATGTGGAAGTTTCCATTGTCTCCCCCCA GAACATGGAAGACAAGGAGATGACTGGGCCCCCGGTGATGTGGAAGTTTCCATTGTCTCCCCCCA A C ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3285751..3286120 32194978 MeRIP-seq:(Medium) rs749886081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12728152,Human_RBP_ID_18678792 Human_Splice_Rec_1669542,Human_Splice_Rec_1669543,Human_Splice_Rec_1669550,Human_Splice_Rec_1669551 RMVar_hsa_circ_119880,RMVar_hsa_circ_30976,RMVar_hsa_circ_41504,RMVar_hsa_circ_175845 73260 RMVar_ID_73260 Human_SNP_ID_591575053 m1A Human chr16 + 3289780 3289780 3289780 CTTTGGTGGGAACCCACGTTTCCTGTCACTACACAGAGCACACCTGGGAGAGGAGGCCCACAAGT CTTTGGTGGGAACCCACGTTTCCTGTCACTACCCAGAGCACACCTGGGAGAGGAGGCCCACAAGT A C ZNF263 Ensembl:ENSG00000006194 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3289409..3289959 32194978 MeRIP-seq:(Medium) rs769807273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4367653,Human_RBP_ID_17876324,Human_RBP_ID_22201760 73261 RMVar_ID_73261 Human_SNP_ID_591575067 m1A Human chr16 + 3289809 3289809 3289809 TACACAGAGCACACCTGGGAGAGGAGGCCCACAAGTGCCTTGAATGTGGGAAATGCTTCAGTCAG TACACAGAGCACACCTGGGAGAGGAGGCCCACGAGTGCCTTGAATGTGGGAAATGCTTCAGTCAG A G ZNF263 Ensembl:ENSG00000006194 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3289758..3290309 32194978 MeRIP-seq:(Medium) rs774649019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17876325 73262 RMVar_ID_73262 Human_SNP_ID_591581043 m1A Human chr16 + 3308858 3308858 3308858 CATGGAATGGGGTGAGAAGAAAGATTCCTGACATGTACAGTGAAATAGGATGCAGGTGGATATAG CATGGAATGGGGTGAGAAGAAAGATTCCTGACGTGTACAGTGAAATAGGATGCAGGTGGATATAG A G ZNF75A Ensembl:ENSG00000162086 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3308818..3308963 26863196 MeRIP-seq:(Medium) rs1005560400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1281966 RMVar_hsa_circ_175846,RMVar_hsa_circ_296235,RMVar_hsa_circ_340815,RMVar_hsa_circ_175847 73263 RMVar_ID_73263 Human_SNP_ID_591604208 m1A Human chr16 - 3383230 3383228 3383230 TCCAACCTCACTGCCCACCTACGAACTCACACAGGGGAGAGGCCCTATCAGTGTGGGCAATGTGG TCCAACCTCACTGCCCACCTACGAACTCACAC__GGGAGAGGCCCTATCAGTGTGGGCAATGTGG CCT C ZSCAN32 Ensembl:ENSG00000140987 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3382972..3383271 32194978 MeRIP-seq:(Medium) rs746042756 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17876440,Human_RBP_ID_27442459 73264 RMVar_ID_73264 Human_SNP_ID_591604210 m1A Human chr16 - 3383230 3383229 3383230 TCCAACCTCACTGCCCACCTACGAACTCACACAGGGGAGAGGCCCTATCAGTGTGGGCAATGTGG TCCAACCTCACTGCCCACCTACGAACTCACAC_GGGGAGAGGCCCTATCAGTGTGGGCAATGTGG CT C ZSCAN32 Ensembl:ENSG00000140987 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3382972..3383271 32194978 MeRIP-seq:(Medium) rs1567299226 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17876440,Human_RBP_ID_27442459 73265 RMVar_ID_73265 Human_SNP_ID_591604211 m1A Human chr16 - 3383230 3383230 3383230 TCCAACCTCACTGCCCACCTACGAACTCACACAGGGGAGAGGCCCTATCAGTGTGGGCAATGTGG TCCAACCTCACTGCCCACCTACGAACTCACACGGGGGAGAGGCCCTATCAGTGTGGGCAATGTGG T C ZSCAN32 Ensembl:ENSG00000140987 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3382972..3383271 32194978 MeRIP-seq:(Medium) rs764437668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17876440,Human_RBP_ID_27442459 73266 RMVar_ID_73266 Human_SNP_ID_591604656 m1A Human chr16 - 3384555 3384555 3384555 AGAATGGGGAACCCACGGAGGTAGAAGATGGCACTGTGGATGGTGCAGACAGGGATGAAAAGGAC AGAATGGGGAACCCACGGAGGTAGAAGATGGCGCTGTGGATGGTGCAGACAGGGATGAAAAGGAC T C ZSCAN32 Ensembl:ENSG00000140987 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3384457..3384558 32194978 MeRIP-seq:(Medium) rs1327528318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12728645 Human_Splice_Rec_1669659,Human_Splice_Rec_1669671,Human_Splice_Rec_1669681,Human_Splice_Rec_1669687,Human_Splice_Rec_1669691 RMVar_hsa_circ_29572 73267 RMVar_ID_73267 Human_SNP_ID_591604812 m1A Human chr16 - 3384914 3384914 3384914 CCCAGCAACAGGTGTGCCCTGGGGCTATGAAGAGACCAAGACGCTCCTGGCTATTCTTAGTAGTT CCCAGCAACAGGTGTGCCCTGGGGCTATGAAGGGACCAAGACGCTCCTGGCTATTCTTAGTAGTT T C ZSCAN32 Ensembl:ENSG00000140987 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3384804..3390029 32194978 MeRIP-seq:(Medium) rs759087681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1669658,Human_Splice_Rec_1669670,Human_Splice_Rec_1669680,Human_Splice_Rec_1669686,Human_Splice_Rec_1669690,Human_Splice_Rec_1669720,Human_Splice_Rec_1669726,Human_Splice_Rec_1669728,Human_Splice_Rec_1669730,Human_Splice_Rec_1669736,Human_Splice_Rec_1669740,Human_Splice_Rec_1669748 RMVar_hsa_circ_29572 73268 RMVar_ID_73268 Human_SNP_ID_591606098 m1A Human chr16 + 3389763 3389763 3389763 TCTGGACTACTTGTTCTGACTCTGTCTCACTAACATTTTGCTTCTCCACCGCCTCACCCTTCACC TCTGGACTACTTGTTCTGACTCTGTCTCACTATCATTTTGCTTCTCCACCGCCTCACCCTTCACC A T AC025283.2 Ensembl:ENSG00000285329 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3389762..3389892 26863196 MeRIP-seq:(Medium) rs182791675 Functional Loss SNV dbSNP153 33..33 33 - - - 73269 RMVar_ID_73269 Human_SNP_ID_591607824 m1A Human chr16 - 3394759 3394759 3394759 GGAAGAAGGGAGGGCTTGTGGCTGGAGCTCAGAGACTGGGGAAGAGTGCTGTGAGAGAAAGGGAG GGAAGAAGGGAGGGCTTGTGGCTGGAGCTCAGCGACTGGGGAAGAGTGCTGTGAGAGAAAGGGAG T G ZSCAN32 Ensembl:ENSG00000140987 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3394720..3395031 26863196 MeRIP-seq:(Medium) rs987844056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29572,RMVar_hsa_circ_359131 73270 RMVar_ID_73270 Human_SNP_ID_591622898 m1A Human chr16 + 3443778 3443775 3443778 GGGTGACCCCAGGGGGACGTAATGTTTCCGAGAAGAAGGACAGAAAGAAGACTGGGAGACACCGG GGGTGACCCCAGGGGGACGTAATGTTTCCG___AGAAGGACAGAAAGAAGACTGGGAGACACCGG GAGA G NAA60,AC025283.2 Ensembl:ENSG00000122390,Ensembl:ENSG00000285329 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3443728..3443862 26863196 MeRIP-seq:(Medium) rs753871113 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_891360,Human_RBP_ID_4367989,Human_RBP_ID_18418649 Human_Splice_Rec_1669777,Human_Splice_Rec_1669789,Human_Splice_Rec_1669797,Human_Splice_Rec_1669799,Human_Splice_Rec_1669803,Human_Splice_Rec_1669811,Human_Splice_Rec_1669823,Human_Splice_Rec_1669843,Human_Splice_Rec_1669863,Human_Splice_Rec_1669869,Human_Splice_Rec_1669879,Human_Splice_Rec_1669883,Human_Splice_Rec_1669895,Human_Splice_Rec_1669899,Human_Splice_Rec_1669905 73271 RMVar_ID_73271 Human_SNP_ID_591642112 m1A Human chr16 - 3501075 3501075 3501075 GGCGCGGGGCTGCCTTACTGCGGAGGTCGCGGAAAGACATAACGCTCAGGTCCCCAGGAGCCCAG GGCGCGGGGCTGCCTTACTGCGGAGGTCGCGGGAAGACATAACGCTCAGGTCCCCAGGAGCCCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3448536..3506412 32194978 MeRIP-seq:(Medium) rs1277917152 Functional Loss SNV dbSNP153 33..33 33 - - - 73272 RMVar_ID_73272 Human_SNP_ID_591667232 m1A Human chr16 - 3581338 3581338 3581338 CATGTTCACTAGCGGATTCCATTCTTTGGGTTAAAGCTGCCTCCAGCCTCAGGAGCAGTGTGGAG CATGTTCACTAGCGGATTCCATTCTTTGGGTTGAAGCTGCCTCCAGCCTCAGGAGCAGTGTGGAG T C SLX4 Ensembl:ENSG00000188827 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs75773027 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_319,Clinvar_Rec_320,Clinvar_Rec_321,Clinvar_Rec_322,Clinvar_Rec_323,Clinvar_Rec_324,Clinvar_Rec_2691,Clinvar_Rec_2692,Clinvar_Rec_2693,Clinvar_Rec_2694,Clinvar_Rec_2695,Clinvar_Rec_2696 GWAS_ID_8882,GWAS_ID_8883,GWAS_ID_8884 73273 RMVar_ID_73273 Human_SNP_ID_591667554 m1A Human chr16 - 3582334 3582334 3582334 CAAGAAGAAGGTGGAGCGGAACTGATGGGGCCATCCCGACCCCACCCCAACCTGCCATCAGCAGC CAAGAAGAAGGTGGAGCGGAACTGATGGGGCCGTCCCGACCCCACCCCAACCTGCCATCAGCAGC T C SLX4 Ensembl:ENSG00000188827 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3751839 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_325 GWAS_ID_8885,GWAS_ID_8886,GWAS_ID_8887,GWAS_ID_8888,GWAS_ID_8889,GWAS_ID_8890,GWAS_ID_8891,GWAS_ID_8892,GWAS_ID_8893,GWAS_ID_8894 73274 RMVar_ID_73274 Human_SNP_ID_591676241 m1A Human chr16 - 3608546 3608546 3608546 AGCAAGTGAACCGGCCCACTCTGTGAATGGGGAGGGGGGTGTGCTTGCCTCTGCTCCAGATCCAC AGCAAGTGAACCGGCCCACTCTGTGAATGGGGGGGGGGGTGTGCTTGCCTCTGCTCCAGATCCAC T C SLX4 Ensembl:ENSG00000188827 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3608497..3608581 32194978 MeRIP-seq:(Medium) rs1433068604 Functional Loss SNV dbSNP153 33..33 33 - - - 73275 RMVar_ID_73275 Human_SNP_ID_591677357 m1A Human chr16 - 3611814 3611810 3611814 TCACAGCTGCCACAGTGCCTTAAACTCGCCCTAACTCTTTCTCAAAAACTAACAGACTCCACCTG TCACAGCTGCCACAGTGCCTTAAACTCGCCCT____CTTTCTCAAAAACTAACAGACTCCACCTG GAGTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3611763..3612040 26863196 MeRIP-seq:(Medium) rs1335552988 Functional Loss DEL dbSNP153 33..36 33 - - - 73276 RMVar_ID_73276 Human_SNP_ID_591677359 m1A Human chr16 - 3611814 3611814 3611814 TCACAGCTGCCACAGTGCCTTAAACTCGCCCTAACTCTTTCTCAAAAACTAACAGACTCCACCTG TCACAGCTGCCACAGTGCCTTAAACTCGCCCTGACTCTTTCTCAAAAACTAACAGACTCCACCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3611763..3612040 26863196 MeRIP-seq:(Medium) rs12924990 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8895,GWAS_ID_8896,GWAS_ID_8897,GWAS_ID_8898,GWAS_ID_8899,GWAS_ID_8900,GWAS_ID_8901 73277 RMVar_ID_73277 Human_SNP_ID_591677360 m1A Human chr16 - 3611814 3611814 3611814 TCACAGCTGCCACAGTGCCTTAAACTCGCCCTAACTCTTTCTCAAAAACTAACAGACTCCACCTG TCACAGCTGCCACAGTGCCTTAAACTCGCCCTCACTCTTTCTCAAAAACTAACAGACTCCACCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3611763..3612040 26863196 MeRIP-seq:(Medium) rs12924990 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8895,GWAS_ID_8896,GWAS_ID_8897,GWAS_ID_8898,GWAS_ID_8899,GWAS_ID_8900,GWAS_ID_8901 73278 RMVar_ID_73278 Human_SNP_ID_591695016 m1A Human chr16 - 3662102 3662102 3662102 AGGTGACCCTCCGACTGGACACCCACCCTGCCATGGTCACCGTGCTGGAGATGGGGGCTGCCCGC AGGTGACCCTCCGACTGGACACCCACCCTGCCGTGGTCACCGTGCTGGAGATGGGGGCTGCCCGC T C TRAP1 Ensembl:ENSG00000126602 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3662051..3662185 32194978 MeRIP-seq:(Medium) rs1245215356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473825,Human_RBP_ID_3948652,Human_RBP_ID_4368254,Human_RBP_ID_8433395,Human_RBP_ID_8807604,Human_RBP_ID_9285575,Human_RBP_ID_9372136,Human_RBP_ID_18189855,Human_RBP_ID_18679073,Human_RBP_ID_22440842,Human_RBP_ID_26809934 Human_Splice_Rec_1670574,Human_Splice_Rec_1670602,Human_Splice_Rec_1670634 RMVar_hsa_circ_110778,RMVar_hsa_circ_124575,RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_113469,RMVar_hsa_circ_116781,RMVar_hsa_circ_112201,RMVar_hsa_circ_175888,RMVar_hsa_circ_104500,RMVar_hsa_circ_110180,RMVar_hsa_circ_104546,RMVar_hsa_circ_175892,RMVar_hsa_circ_94974,RMVar_hsa_circ_96441,RMVar_hsa_circ_77833,RMVar_hsa_circ_175893,RMVar_hsa_circ_175890,RMVar_hsa_circ_175891,RMVar_hsa_circ_175889,RMVar_hsa_circ_175884,RMVar_hsa_circ_175886,RMVar_hsa_circ_175887,RMVar_hsa_circ_175885,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_127249,RMVar_hsa_circ_175896,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350 73279 RMVar_ID_73279 Human_SNP_ID_591695025 m1A Human chr16 - 3662116 3662116 3662116 CGGGCTTTGCTCACAGGTGACCCTCCGACTGGACACCCACCCTGCCATGGTCACCGTGCTGGAGA CGGGCTTTGCTCACAGGTGACCCTCCGACTGGGCACCCACCCTGCCATGGTCACCGTGCTGGAGA T C TRAP1 Ensembl:ENSG00000126602 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs751629562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473825,Human_RBP_ID_8433395,Human_RBP_ID_8807604,Human_RBP_ID_9285575,Human_RBP_ID_9372137,Human_RBP_ID_17876594,Human_RBP_ID_18189855,Human_RBP_ID_18679073,Human_RBP_ID_22440842 Human_Splice_Rec_1670574,Human_Splice_Rec_1670602,Human_Splice_Rec_1670634 RMVar_hsa_circ_110778,RMVar_hsa_circ_124575,RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_113469,RMVar_hsa_circ_116781,RMVar_hsa_circ_112201,RMVar_hsa_circ_175888,RMVar_hsa_circ_104500,RMVar_hsa_circ_110180,RMVar_hsa_circ_104546,RMVar_hsa_circ_175892,RMVar_hsa_circ_94974,RMVar_hsa_circ_96441,RMVar_hsa_circ_77833,RMVar_hsa_circ_175893,RMVar_hsa_circ_175890,RMVar_hsa_circ_175891,RMVar_hsa_circ_175889,RMVar_hsa_circ_175884,RMVar_hsa_circ_175886,RMVar_hsa_circ_175887,RMVar_hsa_circ_175885,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_127249,RMVar_hsa_circ_175896,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350 73280 RMVar_ID_73280 Human_SNP_ID_591695029 m1A Human chr16 + 3662119 3662119 3662119 CCAGCACGGTGACCATGGCAGGGTGGGTGTCCAGTCGGAGGGTCACCTGTGAGCAAAGCCCGGGG CCAGCACGGTGACCATGGCAGGGTGGGTGTCCGGTCGGAGGGTCACCTGTGAGCAAAGCCCGGGG A G DNASE1 Ensembl:ENSG00000213918 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3661952..3662177 26863196 MeRIP-seq:(Medium) rs1234370208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175895 73281 RMVar_ID_73281 Human_SNP_ID_591695470 m1A Human chr16 - 3662951 3662951 3662951 GCCTGCTCTTCCGCAGCCGCCGAGTGCCTATCAGAGAAGGAGACGGAGGAGCTCATGGCCTGGAT GCCTGCTCTTCCGCAGCCGCCGAGTGCCTATCGGAGAAGGAGACGGAGGAGCTCATGGCCTGGAT T C TRAP1 Ensembl:ENSG00000126602 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3662847..3663018 26863196 MeRIP-seq:(Medium) rs1285598616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947214,Human_RBP_ID_4400168,Human_RBP_ID_8812217,Human_RBP_ID_9285577,Human_RBP_ID_12730169,Human_RBP_ID_17652901,Human_RBP_ID_18189856,Human_RBP_ID_18983099,Human_RBP_ID_20168863,Human_RBP_ID_22441247,Human_RBP_ID_25208499,Human_RBP_ID_26329718,Human_RBP_ID_27811533 Human_Splice_Rec_1670572,Human_Splice_Rec_1670573,Human_Splice_Rec_1670600,Human_Splice_Rec_1670601,Human_Splice_Rec_1670632,Human_Splice_Rec_1670633 Human_miRNA_ID_1023677,Human_miRNA_ID_3118445 RMVar_hsa_circ_110778,RMVar_hsa_circ_124575,RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_112201,RMVar_hsa_circ_175888,RMVar_hsa_circ_104500,RMVar_hsa_circ_110180,RMVar_hsa_circ_104546,RMVar_hsa_circ_175892,RMVar_hsa_circ_94974,RMVar_hsa_circ_96441,RMVar_hsa_circ_77833,RMVar_hsa_circ_175890,RMVar_hsa_circ_175891,RMVar_hsa_circ_175889,RMVar_hsa_circ_175884,RMVar_hsa_circ_175886,RMVar_hsa_circ_175887,RMVar_hsa_circ_175885,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_84054,RMVar_hsa_circ_127249,RMVar_hsa_circ_175896,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_80532,RMVar_hsa_circ_83997,RMVar_hsa_circ_175898,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_175897 73282 RMVar_ID_73282 Human_SNP_ID_591696156 m1A Human chr16 - 3664375 3664375 3664375 AGCTAACCAGCCTCTCAGAATACGCCAGCCGCATGCGGGCCGGCACCCGCAACATCTACTACCTG AGCTAACCAGCCTCTCAGAATACGCCAGCCGCGTGCGGGCCGGCACCCGCAACATCTACTACCTG T C TRAP1 Ensembl:ENSG00000126602 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr16:3664326..3664450;chr16:3664326..3664399 26863196 MeRIP-seq:(Medium) rs1486402841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473836,Human_RBP_ID_18189858,Human_RBP_ID_22581869,Human_RBP_ID_22760065,Human_RBP_ID_26809940 Human_Splice_Rec_1670568,Human_Splice_Rec_1670596,Human_Splice_Rec_1670628 RMVar_hsa_circ_124575,RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_112201,RMVar_hsa_circ_175888,RMVar_hsa_circ_104500,RMVar_hsa_circ_110180,RMVar_hsa_circ_94974,RMVar_hsa_circ_96441,RMVar_hsa_circ_77833,RMVar_hsa_circ_175890,RMVar_hsa_circ_175889,RMVar_hsa_circ_175884,RMVar_hsa_circ_175886,RMVar_hsa_circ_175887,RMVar_hsa_circ_175885,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_52129,RMVar_hsa_circ_84054,RMVar_hsa_circ_127249,RMVar_hsa_circ_175896,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_80532,RMVar_hsa_circ_83997,RMVar_hsa_circ_175898,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_175897 73283 RMVar_ID_73283 Human_SNP_ID_591700055 m1A Human chr16 + 3674458 3674458 3674458 CGCGACGTAGCGGTAGAACTCCTCATGTTGCCACTCACGGACATCCTTGGGGTCCATCATCCAGA CGCGACGTAGCGGTAGAACTCCTCATGTTGCCGCTCACGGACATCCTTGGGGTCCATCATCCAGA A G DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3672776..3674500 32194978 MeRIP-seq:(Medium) rs753342714 Functional Loss SNV dbSNP153 33..33 33 - - - 73284 RMVar_ID_73284 Human_SNP_ID_591701403 m1A Human chr16 + 3677460 3677460 3677460 CTTTCCAAACTCCATGCTAAGGGCTCCAGCTCAGCTTTGAGCTGCCTGTCAGGCGACATTCGTCA CTTTCCAAACTCCATGCTAAGGGCTCCAGCTCCGCTTTGAGCTGCCTGTCAGGCGACATTCGTCA A C DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3677459..3677573 26863196 MeRIP-seq:(Medium) rs577853868 Functional Loss SNV dbSNP153 33..33 33 - - - 73285 RMVar_ID_73285 Human_SNP_ID_591701404 m1A Human chr16 + 3677460 3677460 3677460 CTTTCCAAACTCCATGCTAAGGGCTCCAGCTCAGCTTTGAGCTGCCTGTCAGGCGACATTCGTCA CTTTCCAAACTCCATGCTAAGGGCTCCAGCTCGGCTTTGAGCTGCCTGTCAGGCGACATTCGTCA A G DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3677459..3677573 26863196 MeRIP-seq:(Medium) rs577853868 Functional Loss SNV dbSNP153 33..33 33 - - - 73286 RMVar_ID_73286 Human_SNP_ID_591715889 m1A Human chr16 - 3717498 3717498 3717498 CGCGGCGCTCTGGGAGTACGACATGGCGCGCGAGCTGCGGGCGCTGCTGCTGTGGGGCCGCCGCC CGCGGCGCTCTGGGAGTACGACATGGCGCGCGGGCTGCGGGCGCTGCTGCTGTGGGGCCGCCGCC T C TRAP1 Ensembl:ENSG00000126602 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:3717373..3717550;chr16:3717323..3717550 26863196 MeRIP-seq:(Medium) rs1439206349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473875,Human_RBP_ID_761239,Human_RBP_ID_4392814,Human_RBP_ID_5465160,Human_RBP_ID_8433494,Human_RBP_ID_8811712,Human_RBP_ID_9285594,Human_RBP_ID_9324906,Human_RBP_ID_17876628,Human_RBP_ID_18419445,Human_RBP_ID_18469662,Human_RBP_ID_21971082,Human_RBP_ID_22441251 Human_Splice_Rec_1670545,Human_Splice_Rec_1670607,Human_Splice_Rec_1670683,Human_Splice_Rec_1670695,Human_Splice_Rec_1670699,Human_Splice_Rec_1670711,Human_Splice_Rec_1670719 Human_miRNA_ID_2101519,Human_miRNA_ID_2107474,Human_miRNA_ID_2113415,Human_miRNA_ID_2165965,Human_miRNA_ID_2597211,Human_miRNA_ID_2740123,Human_miRNA_ID_2756851,Human_miRNA_ID_3040716 RMVar_hsa_circ_104500,RMVar_hsa_circ_175881,RMVar_hsa_circ_121533,RMVar_hsa_circ_175902,RMVar_hsa_circ_102397,RMVar_hsa_circ_175910 73287 RMVar_ID_73287 Human_SNP_ID_591715915 m1A Human chr16 + 3717522 3717522 3717522 CCCGCAGCTCGCGCGCCATGTCGTACTCCCAGAGCGCCGCGCGCAGCCACGCGGGACCGTACACG CCCGCAGCTCGCGCGCCATGTCGTACTCCCAGCGCGCCGCGCGCAGCCACGCGGGACCGTACACG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3717476..3717550 26863196 MeRIP-seq:(Medium) rs922184950 Functional Loss SNV dbSNP153 33..33 33 - - - 73288 RMVar_ID_73288 Human_SNP_ID_591715916 m1A Human chr16 + 3717522 3717522 3717522 CCCGCAGCTCGCGCGCCATGTCGTACTCCCAGAGCGCCGCGCGCAGCCACGCGGGACCGTACACG CCCGCAGCTCGCGCGCCATGTCGTACTCCCAGGGCGCCGCGCGCAGCCACGCGGGACCGTACACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3717476..3717550 26863196 MeRIP-seq:(Medium) rs922184950 Functional Loss SNV dbSNP153 33..33 33 - - - 73289 RMVar_ID_73289 Human_SNP_ID_591719493 m1A Human chr16 + 3727994 3727994 3727994 CTGGAATGTGGAGGCTGGGACTGGGGCCGTGGAGACTGGACAGGGGCTGGAGACCGCACCTGGTT CTGGAATGTGGAGGCTGGGACTGGGGCCGTGGGGACTGGACAGGGGCTGGAGACCGCACCTGGTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3727951..3728121 26863196 MeRIP-seq:(Medium) rs1462080104 Functional Loss SNV dbSNP153 33..33 33 - - - 73290 RMVar_ID_73290 Human_SNP_ID_591720188 m1A Human chr16 + 3729276 3729276 3729276 TGGACACCGTGGTGGGGGGCTGAGTCCGGGCCACGCTGGGGAAGCCAGCTGGTGACATGCTCACG TGGACACCGTGGTGGGGGGCTGAGTCCGGGCCGCGCTGGGGAAGCCAGCTGGTGACATGCTCACG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3729227..3729500 26863196 MeRIP-seq:(Medium) rs1440955568 Functional Loss SNV dbSNP153 33..33 33 - - - 73291 RMVar_ID_73291 Human_SNP_ID_591720238 m1A Human chr16 + 3729395 3729395 3729395 TGTGTGGGGGTCCCGGGCGGTGCTGAGGTAGGAGAAGGCAGACTCTGCTGAGGCACGTTGCGGGT TGTGTGGGGGTCCCGGGCGGTGCTGAGGTAGGGGAAGGCAGACTCTGCTGAGGCACGTTGCGGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3729226..3729605 26863196 MeRIP-seq:(Medium) rs1201270413 Functional Loss SNV dbSNP153 33..33 33 - - - 73292 RMVar_ID_73292 Human_SNP_ID_591721124 m1A Human chr16 - 3731871 3731871 3731871 AGAACAACAAGAAAACCAACAAGAACAAAAGCAGCATCAGCCGCGCCAACAAGAAGAAGCCCAGC AGAACAACAAGAAAACCAACAAGAACAAAAGCGGCATCAGCCGCGCCAACAAGAAGAAGCCCAGC T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3731820..3731953 26863196 MeRIP-seq:(Medium) rs766942126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45939,Human_RBP_ID_9372154,Human_RBP_ID_24544370,Human_RBP_ID_26328575 Human_Splice_Rec_1670782,Human_Splice_Rec_1670783,Human_Splice_Rec_1670840,Human_Splice_Rec_1670841,Human_Splice_Rec_1670850,Human_Splice_Rec_1670858 RMVar_hsa_circ_34329,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959 73293 RMVar_ID_73293 Human_SNP_ID_591721132 m1A Human chr16 - 3731901 3731899 3731902 GTCAGGGCGACAGCAAGAATGCCAAGAAGAAGAACAACAAGAAAACCAACAAGAACAAAAGCAGC GTCAGGGCGACAGCAAGAATGCCAAGAAGAA___CAACAAGAAAACCAACAAGAACAAAAGCAGC GTTC G CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3731851..3731925 26863196 MeRIP-seq:(Medium) rs751071525 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9372155,Human_RBP_ID_24544677,Human_RBP_ID_26328576 Human_Splice_Rec_1670782,Human_Splice_Rec_1670840,Human_Splice_Rec_1670850,Human_Splice_Rec_1670858 RMVar_hsa_circ_34329,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959 73294 RMVar_ID_73294 Human_SNP_ID_591722132 m1A Human chr16 - 3734967 3734967 3734967 AGCCCCAGAACTTGGGACAGGCGATTGTGACCAGTGAGGAAAAGCGGTGAATGGAGGTGGCTCTT AGCCCCAGAACTTGGGACAGGCGATTGTGACCGGTGAGGAAAAGCGGTGAATGGAGGTGGCTCTT T C CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3734965..3735150 26863196 MeRIP-seq:(Medium) rs918823206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8084728,Human_RBP_ID_8433523,Human_RBP_ID_17254261,Human_RBP_ID_23688591 RMVar_hsa_circ_268634,RMVar_hsa_circ_265959 73295 RMVar_ID_73295 Human_SNP_ID_591725996 m1A Human chr16 - 3746421 3746419 3746421 CTGCCACGTGGAAGGGAGAGGTAGCCAGACAGAGCCGGGCTGTCAGAGAGTGCCATAGGACCATG CTGCCACGTGGAAGGGAGAGGTAGCCAGACAG__CCGGGCTGTCAGAGAGTGCCATAGGACCATG GCT G CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3746415..3746513 26863196 MeRIP-seq:(Medium) rs1486406372 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6511916,Human_RBP_ID_12732051 RMVar_hsa_circ_50096,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_10415,RMVar_hsa_circ_15628,RMVar_hsa_circ_175919,RMVar_hsa_circ_21809,RMVar_hsa_circ_329873,RMVar_hsa_circ_288921,RMVar_hsa_circ_175923,RMVar_hsa_circ_345695,RMVar_hsa_circ_93369,RMVar_hsa_circ_320859,RMVar_hsa_circ_59567,RMVar_hsa_circ_175924,RMVar_hsa_circ_175925 73296 RMVar_ID_73296 Human_SNP_ID_591732511 m1A Human chr16 - 3767834 3767834 3767834 AAACAGACATAGCAGAGCAGAAATCAGAACCAATGGAAGTGGATGAAAAGAAACCTGAAGTGAAA AAACAGACATAGCAGAGCAGAAATCAGAACCAGTGGAAGTGGATGAAAAGAAACCTGAAGTGAAA T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3767785..3767892 26863196 MeRIP-seq:(Medium) rs896266657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43595,Human_RBP_ID_895807,Human_RBP_ID_1518226,Human_RBP_ID_9372171,Human_RBP_ID_12732470,Human_RBP_ID_24544472,Human_RBP_ID_26329734,Human_RBP_ID_27811552 Human_Splice_Rec_1670756,Human_Splice_Rec_1670814,Human_Splice_Rec_1670878,Human_Splice_Rec_1670930 RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_175927,RMVar_hsa_circ_93369,RMVar_hsa_circ_320859,RMVar_hsa_circ_59567,RMVar_hsa_circ_175924,RMVar_hsa_circ_307611,RMVar_hsa_circ_338177,RMVar_hsa_circ_175928,RMVar_hsa_circ_175930,RMVar_hsa_circ_366642,RMVar_hsa_circ_374544,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_289624,RMVar_hsa_circ_175933,RMVar_hsa_circ_297195,RMVar_hsa_circ_360705 73297 RMVar_ID_73297 Human_SNP_ID_591733484 m1A Human chr16 - 3770651 3770651 3770651 CAGGCCCAGGTGACCCCGCAGCCTCAAACCCCAGTTCAGCCCCCGTCTGTGGCTACCCCTCAGTC CAGGCCCAGGTGACCCCGCAGCCTCAAACCCCTGTTCAGCCCCCGTCTGTGGCTACCCCTCAGTC T A CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:3770626..3770650 26863196 MeRIP-seq:(Medium) rs1180909512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43597,Human_RBP_ID_4368521,Human_RBP_ID_17256577,Human_RBP_ID_17488357,Human_RBP_ID_18437717,Human_RBP_ID_23688679,Human_RBP_ID_26328585 Human_Splice_Rec_1670753,Human_Splice_Rec_1670811,Human_Splice_Rec_1670875,Human_Splice_Rec_1670927 Human_miRNA_ID_2710012 RMVar_hsa_circ_12577,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_320859,RMVar_hsa_circ_307611,RMVar_hsa_circ_175928,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_114949,RMVar_hsa_circ_360705,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_175936,RMVar_hsa_circ_109495,RMVar_hsa_circ_356220,RMVar_hsa_circ_175937,RMVar_hsa_circ_175938 73298 RMVar_ID_73298 Human_SNP_ID_591733491 m1A Human chr16 - 3770676 3770671 3770677 CACCCCTACAGTCCAGGCAGCAGCCCAGGCCCAGGTGACCCCGCAGCCTCAAACCCCAGTTCAGC CACCCCTACAGTCCAGGCAGCAGCCCAGGCC______ACCCCGCAGCCTCAAACCCCAGTTCAGC TCACCTG T CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3770627..3770890 26863196 MeRIP-seq:(Medium) rs766944517 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_9285597,Human_RBP_ID_17256577,Human_RBP_ID_17488357,Human_RBP_ID_18190401,Human_RBP_ID_26328585 Human_miRNA_ID_2715406,Human_miRNA_ID_3051385 RMVar_hsa_circ_12577,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_320859,RMVar_hsa_circ_307611,RMVar_hsa_circ_175928,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_114949,RMVar_hsa_circ_360705,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_175936,RMVar_hsa_circ_109495,RMVar_hsa_circ_356220,RMVar_hsa_circ_175937,RMVar_hsa_circ_175938 73299 RMVar_ID_73299 Human_SNP_ID_591733506 m1A Human chr16 - 3770722 3770722 3770722 CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTACCCAAACCCAGAGCACCCCTACAGTCCAGGCA CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTTCCCAAACCCAGAGCACCCCTACAGTCCAGGCA T A CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3770551..3770900 26863196 MeRIP-seq:(Medium) rs143247685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9285597,Human_RBP_ID_17256578,Human_RBP_ID_17488358,Human_RBP_ID_18679223,Human_RBP_ID_26328586 Human_miRNA_ID_2425014,Human_miRNA_ID_2434676,Human_miRNA_ID_2908180,Human_miRNA_ID_3027019 Clinvar_Rec_326,Clinvar_Rec_327 RMVar_hsa_circ_12577,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_320859,RMVar_hsa_circ_307611,RMVar_hsa_circ_175928,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_114949,RMVar_hsa_circ_360705,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_175936,RMVar_hsa_circ_109495,RMVar_hsa_circ_356220,RMVar_hsa_circ_175937,RMVar_hsa_circ_175938 73300 RMVar_ID_73300 Human_SNP_ID_591733507 m1A Human chr16 - 3770722 3770722 3770722 CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTACCCAAACCCAGAGCACCCCTACAGTCCAGGCA CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTGCCCAAACCCAGAGCACCCCTACAGTCCAGGCA T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3770551..3770900 26863196 MeRIP-seq:(Medium) rs143247685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9285597,Human_RBP_ID_17256578,Human_RBP_ID_17488358,Human_RBP_ID_18679223,Human_RBP_ID_26328586 Human_miRNA_ID_2425014,Human_miRNA_ID_2434676,Human_miRNA_ID_2908180,Human_miRNA_ID_3027019 Clinvar_Rec_326,Clinvar_Rec_327 RMVar_hsa_circ_12577,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_320859,RMVar_hsa_circ_307611,RMVar_hsa_circ_175928,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_114949,RMVar_hsa_circ_360705,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_175936,RMVar_hsa_circ_109495,RMVar_hsa_circ_356220,RMVar_hsa_circ_175937,RMVar_hsa_circ_175938 73301 RMVar_ID_73301 Human_SNP_ID_591767017 m1A Human chr16 - 3879982 3879960 3879982 GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCGACCCCCGTCCGGGCCCTCGCCGGCCCGGCCGCC GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCG______________________GCCCGGCCGCC CCGGCGAGGGCCCGGACGGGGGT C CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3879937..3880122 26863196 MeRIP-seq:(Medium) rs776020320 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_9324908 RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_84211,RMVar_hsa_circ_175944,RMVar_hsa_circ_119227,RMVar_hsa_circ_175961 73302 RMVar_ID_73302 Human_SNP_ID_591767028 m1A Human chr16 - 3879982 3879971 3879982 GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCGACCCCCGTCCGGGCCCTCGCCGGCCCGGCCGCC GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCG___________GGCCCTCGCCGGCCCGGCCGCC CCGGACGGGGGT C CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3879937..3880122 26863196 MeRIP-seq:(Medium) rs1194429139 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_9324908 RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_84211,RMVar_hsa_circ_175944,RMVar_hsa_circ_119227,RMVar_hsa_circ_175961 73303 RMVar_ID_73303 Human_SNP_ID_591767039 m1A Human chr16 - 3879982 3879982 3879982 GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCGACCCCCGTCCGGGCCCTCGCCGGCCCGGCCGCC GCTCCTCTCCCTCGCAGCCGGCAGGGCCCCCGCCCCCCGTCCGGGCCCTCGCCGGCCCGGCCGCC T G CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3879937..3880122 26863196 MeRIP-seq:(Medium) rs1472159448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9324908 RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_84211,RMVar_hsa_circ_175944,RMVar_hsa_circ_119227,RMVar_hsa_circ_175961 73304 RMVar_ID_73304 Human_SNP_ID_591767069 m1A Human chr16 + 3880009 3880009 3880009 GGGGGTCGGGGGCCCTGCCGGCTGCGAGGGAGAGGAGCGAGCGCGGGCCGCGAGCGGGCGGGCGG GGGGGTCGGGGGCCCTGCCGGCTGCGAGGGAGGGGAGCGAGCGCGGGCCGCGAGCGGGCGGGCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972533,GSM1972534 HEK293T,ALKBH3 KO;HEPG2 cell line,total RNA Untreated chr16:3879908..3880027;chr16:3879937..3880071 26863410,26863196 MeRIP-seq:(Medium) rs1404640070 Functional Loss SNV dbSNP153 33..33 33 - - - 73305 RMVar_ID_73305 Human_SNP_ID_591767220 m1A Human chr16 - 3880320 3880320 3880320 GAATTCATTAAGTGGGGCGCGGGGGGGGAGCGAGGCGGCGGCGGCGGCGGCACCATGTTCTCGGG GAATTCATTAAGTGGGGCGCGGGGGGGGAGCGGGGCGGCGGCGGCGGCGGCACCATGTTCTCGGG T C CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:3880188..3880469;chr16:3879894..3880475;chr16:3880176..3880464 26863196 MeRIP-seq:(Medium) rs1366742365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816472,Human_RBP_ID_4392816,Human_RBP_ID_9324911,Human_RBP_ID_26780131 73306 RMVar_ID_73306 Human_SNP_ID_591767222 m1A Human chr16 - 3880324 3880324 3880324 GAGCGAATTCATTAAGTGGGGCGCGGGGGGGGAGCGAGGCGGCGGCGGCGGCGGCACCATGTTCT GAGCGAATTCATTAAGTGGGGCGCGGGGGGGGGGCGAGGCGGCGGCGGCGGCGGCACCATGTTCT T C CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3880188..3880656 26863196 MeRIP-seq:(Medium) rs1307459191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816472,Human_RBP_ID_4392816,Human_RBP_ID_9324911,Human_RBP_ID_26780131 73307 RMVar_ID_73307 Human_SNP_ID_591767376 m1A Human chr16 - 3880612 3880612 3880612 CCGCCGGTCCCGGGCCCCACAACCGCCCGCGCACCCCGCTCCGCCCGGCCGGCCCGCTCCGCCCG CCGCCGGTCCCGGGCCCCACAACCGCCCGCGCCCCCCGCTCCGCCCGGCCGGCCCGCTCCGCCCG T G CREBBP Ensembl:ENSG00000005339 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3880565..3880689 26863196 MeRIP-seq:(Medium) rs992697235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394332,Human_RBP_ID_9285599 73308 RMVar_ID_73308 Human_SNP_ID_591799079 m1A Human chr16 - 3982160 3982160 3982160 CCAGGACCCTTTCAGCTTCCTCCGAGGCCGCCATGGGCCATGCTGTCTGTGGCGTGTGCTCAGTG CCAGGACCCTTTCAGCTTCCTCCGAGGCCGCCGTGGGCCATGCTGTCTGTGGCGTGTGCTCAGTG T C ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3982154..3982304 32194978 MeRIP-seq:(Medium) rs1456707980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121497,RMVar_hsa_circ_42193,RMVar_hsa_circ_327505,RMVar_hsa_circ_331658,RMVar_hsa_circ_281073,RMVar_hsa_circ_175965,RMVar_hsa_circ_346932,RMVar_hsa_circ_275771,RMVar_hsa_circ_175967,RMVar_hsa_circ_175969,RMVar_hsa_circ_105224,RMVar_hsa_circ_175968,RMVar_hsa_circ_175966 73309 RMVar_ID_73309 Human_SNP_ID_591831409 m1A Human chr16 - 4087845 4087841 4087845 GACAGAAACAAAGAGAAACAAAGAAAAGAGAAAGAAGGAAGGAAGGAAGAGAGAGAGAGAAAGAA GACAGAAACAAAGAGAAACAAAGAAAAGAGAA____GGAAGGAAGGAAGAGAGAGAGAGAAAGAA CTTCT C ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4087796..4087948 26863196 MeRIP-seq:(Medium) rs1359267910 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_2474562 73310 RMVar_ID_73310 Human_SNP_ID_591838355 m1A Human chr16 + 4109721 4109721 4109721 CTTCCTAATGCCACTCAGATCCCATCACCTCCATCACTGCTACTGTAACTTTGGATTGGGCCACC CTTCCTAATGCCACTCAGATCCCATCACCTCCGTCACTGCTACTGTAACTTTGGATTGGGCCACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4109679..4109800 26863196 MeRIP-seq:(Medium) rs900395193 Functional Loss SNV dbSNP153 33..33 33 - - - 73311 RMVar_ID_73311 Human_SNP_ID_591839835 m1A Human chr16 - 4114535 4114535 4114535 CGCCATCGGGGTCCACCTGTTCGTCATGTCCCAGGTGAGGTCCAGGAGCACCTTCCTCAAGGTGG CGCCATCGGGGTCCACCTGTTCGTCATGTCCCTGGTGAGGTCCAGGAGCACCTTCCTCAAGGTGG T A ADCY9 Ensembl:ENSG00000162104 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4114486..4114637 32194978 MeRIP-seq:(Medium) rs757597955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18679331 RMVar_hsa_circ_52892 73312 RMVar_ID_73312 Human_SNP_ID_591840289 m1A Human chr16 + 4115441 4115441 4115441 GATGCAGCAGCTGCTGGTGGGGTGGGGAAGCCATGTTGTCGAGTCCCGGGGCCTGCCCCGGCCGG GATGCAGCAGCTGCTGGTGGGGTGGGGAAGCCTTGTTGTCGAGTCCCGGGGCCTGCCCCGGCCGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4115284..4115483 26863196 MeRIP-seq:(Medium) rs777779866 Functional Loss SNV dbSNP153 33..33 33 - - - 73313 RMVar_ID_73313 Human_SNP_ID_591840454 m1A Human chr16 + 4115840 4115840 4115840 CGCGCGCTCGCCTCCTCCAGCTGCGGCTCCGGAGGGAAGTTCAGACCTTGAGCGCTCCCAGCCCC CGCGCGCTCGCCTCCTCCAGCTGCGGCTCCGGGGGGAAGTTCAGACCTTGAGCGCTCCCAGCCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:4115676..4116175 26863196 MeRIP-seq:(Medium) rs1277327478 Functional Loss SNV dbSNP153 33..33 33 - - - 73314 RMVar_ID_73314 Human_SNP_ID_591840507 m1A Human chr16 + 4115981 4115974 4115981 CAAAGGCGGCGCGCGGCCGGCCCCGGGCCCGGACCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG CAAAGGCGGCGCGCGGCCGGCCCCGG_______CCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG GGCCCGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4115701..4116225 26863196 MeRIP-seq:(Medium) rs1366670966 Functional Loss DEL dbSNP153 27..33 33 - - - 73315 RMVar_ID_73315 Human_SNP_ID_591840513 m1A Human chr16 + 4115981 4115980 4115981 CAAAGGCGGCGCGCGGCCGGCCCCGGGCCCGGACCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG CAAAGGCGGCGCGCGGCCGGCCCCGGGCCCGG_CCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4115701..4116225 26863196 MeRIP-seq:(Medium) rs1391025768 Functional Loss DEL dbSNP153 33..33 33 - - - 73316 RMVar_ID_73316 Human_SNP_ID_591840514 m1A Human chr16 + 4115981 4115981 4115981 CAAAGGCGGCGCGCGGCCGGCCCCGGGCCCGGACCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG CAAAGGCGGCGCGCGGCCGGCCCCGGGCCCGGTCCCCGACCCGGAGCAGCGAGCTTCGGCGGGCG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4115701..4116225 26863196 MeRIP-seq:(Medium) rs1374253835 Functional Loss SNV dbSNP153 33..33 33 - - - 73317 RMVar_ID_73317 Human_SNP_ID_591840674 m1A Human chr16 - 4116399 4116399 4116399 GCGGGGCAGGGGCCGGAGATGGTGGCGGCGGCAGCTCTTCCGACATGAGGCAGCGGCCGCGGGGG GCGGGGCAGGGGCCGGAGATGGTGGCGGCGGCGGCTCTTCCGACATGAGGCAGCGGCCGCGGGGG T C ADCY9 Ensembl:ENSG00000162104 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:4116276..4116452 26863196 MeRIP-seq:(Medium) rs1195784942 Functional Loss SNV dbSNP153 33..33 33 - - - 73318 RMVar_ID_73318 Human_SNP_ID_591885137 m1A Human chr16 - 4257480 4257480 4257480 CCCCCTTCCCCATCTCGGCACTAGAATTCGCCACTCTCCCACCCCCCAGCCCCCACCTCTGCCTC CCCCCTTCCCCATCTCGGCACTAGAATTCGCCCCTCTCCCACCCCCCAGCCCCCACCTCTGCCTC T G TFAP4 Ensembl:ENSG00000090447 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4257430..4257546 26863196 MeRIP-seq:(Medium) rs1188376905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12735988,Human_RBP_ID_17876798,Human_RBP_ID_25209808,Human_RBP_ID_26441199 Human_miRNA_ID_2685373 RMVar_hsa_circ_175971,RMVar_hsa_circ_94857 73319 RMVar_ID_73319 Human_SNP_ID_591885410 m1A Human chr16 - 4258203 4258203 4258203 CGAGGGCACCCAGGAAAAGCAGGAGCTGGAGGAGGAGCAGCGGCGAGCTGTCATCGTGAAGCCTG CGAGGGCACCCAGGAAAAGCAGGAGCTGGAGGGGGAGCAGCGGCGAGCTGTCATCGTGAAGCCTG T C TFAP4 Ensembl:ENSG00000090447 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4258153..4258264 26863196 MeRIP-seq:(Medium) rs768098928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6512946 Human_Splice_Rec_1671106,Human_Splice_Rec_1671114,Human_Splice_Rec_1671120 RMVar_hsa_circ_175971,RMVar_hsa_circ_94857 73320 RMVar_ID_73320 Human_SNP_ID_591885411 m1A Human chr16 - 4258203 4258203 4258203 CGAGGGCACCCAGGAAAAGCAGGAGCTGGAGGAGGAGCAGCGGCGAGCTGTCATCGTGAAGCCTG CGAGGGCACCCAGGAAAAGCAGGAGCTGGAGGCGGAGCAGCGGCGAGCTGTCATCGTGAAGCCTG T G TFAP4 Ensembl:ENSG00000090447 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4258153..4258264 26863196 MeRIP-seq:(Medium) rs768098928 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6512946 Human_Splice_Rec_1671106,Human_Splice_Rec_1671114,Human_Splice_Rec_1671120 RMVar_hsa_circ_175971,RMVar_hsa_circ_94857 73321 RMVar_ID_73321 Human_SNP_ID_591885918 m1A Human chr16 - 4260072 4260070 4260072 GACACCATCGTGCAGGTACCTGAGCTTGAGAAAGGGGCAGCTTGTGGGGGTCATACTCCGGGAAC GACACCATCGTGCAGGTACCTGAGCTTGAGAA__GGGCAGCTTGTGGGGGTCATACTCCGGGAAC CCT C TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4260064..4260177 26863196 MeRIP-seq:(Medium) rs756610300 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_19073174 73322 RMVar_ID_73322 Human_SNP_ID_591885935 m1A Human chr16 + 4260139 4260138 4260140 GATTTTGCCGGGATGTGGAAACAGAGTTGATGACCGAGGAGGGGCCCATGGTGACGACATTGATG GATTTTGCCGGGATGTGGAAACAGAGTTGATG__CGAGGAGGGGCCCATGGTGACGACATTGATG GAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4260067..4260177 26863196 MeRIP-seq:(Medium) rs1257008958 Functional Loss DEL dbSNP153 33..34 33 - - - 73323 RMVar_ID_73323 Human_SNP_ID_591886516 m1A Human chr16 + 4261852 4261852 4261852 GCTGCTGCCGCAGCTCAATCATCTCCCGCCGCAGGTCCTCCGCCTTCTCGTCCTCCCAGATGTCC GCTGCTGCCGCAGCTCAATCATCTCCCGCCGCTGGTCCTCCGCCTTCTCGTCCTCCCAGATGTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4261801..4261982 26863196 MeRIP-seq:(Medium) rs1252690291 Functional Loss SNV dbSNP153 33..33 33 - - - 73324 RMVar_ID_73324 Human_SNP_ID_591888151 m1A Human chr16 - 4267571 4267571 4267571 GGGCAGGAGGGATAGGTACCTGGCAGGGTTCTAGACTTGAAGGGCATGCCCCATGCCTCCAAGTG GGGCAGGAGGGATAGGTACCTGGCAGGGTTCTGGACTTGAAGGGCATGCCCCATGCCTCCAAGTG T C TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4267568..4267688 26863196 MeRIP-seq:(Medium) rs1038485842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18482112 RMVar_hsa_circ_2265 73325 RMVar_ID_73325 Human_SNP_ID_591888210 m1A Human chr16 + 4267778 4267778 4267778 GGGAAAGTCCACACGGGATTCTCCCAAACCCAAAAAAGCACTAAGGCACTCATCCTTCTCTAACC GGGAAAGTCCACACGGGATTCTCCCAAACCCAGAAAAGCACTAAGGCACTCATCCTTCTCTAACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4267770..4267981 26863196 MeRIP-seq:(Medium) rs555254237 Functional Loss SNV dbSNP153 33..33 33 - - - 73326 RMVar_ID_73326 Human_SNP_ID_591889506 m1A Human chr16 + 4272034 4272034 4272034 CCCGGGCGCGGGCGGGCGAGCGAGCGGCAGCCAACGTGCCCCGGGCCGCGGCGCCCCTACCGGCC CCCGGGCGCGGGCGGGCGAGCGAGCGGCAGCCGACGTGCCCCGGGCCGCGGCGCCCCTACCGGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4272029..4272218 26863196 MeRIP-seq:(Medium) rs1326741989 Functional Loss SNV dbSNP153 33..33 33 - - - 73327 RMVar_ID_73327 Human_SNP_ID_591889759 m1A Human chr16 - 4272767 4272767 4272767 TTCTCCGGCTGATCGCGGGACCTGGCTCGTGCAGAGGAGGGGGGCCGATCGCTATGGAGTATTTC TTCTCCGGCTGATCGCGGGACCTGGCTCGTGCGGAGGAGGGGGGCCGATCGCTATGGAGTATTTC T C TFAP4 Ensembl:ENSG00000090447 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4272717..4272954 26863196 MeRIP-seq:(Medium) rs201281864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4369076,Human_RBP_ID_6512966,Human_RBP_ID_12736121,Human_RBP_ID_26809951 73328 RMVar_ID_73328 Human_SNP_ID_591893096 m1A Human chr16 - 4283485 4283479 4283485 GACCCACTTGAGGGTATGGATCAGGCACTTAAAAATAAGAGCAGTGGCAGGCTGGGCGCGATGGC GACCCACTTGAGGGTATGGATCAGGCACTTAA______GAGCAGTGGCAGGCTGGGCGCGATGGC CTTATTT C lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS0000D5DCB2 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4283475..4283579 26863196 MeRIP-seq:(Medium) rs1266143079 Functional Loss DEL dbSNP153 33..38 33 - - - 73329 RMVar_ID_73329 Human_SNP_ID_591894007 m1A Human chr16 - 4286417 4286417 4286417 GAGAACAACCTATCCTCACCTCTGCAGCAGCCACCTTTGCCGACAGCTCTTCCTCCTGGCTGCAG GAGAACAACCTATCCTCACCTCTGCAGCAGCCGCCTTTGCCGACAGCTCTTCCTCCTGGCTGCAG T C lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS0000D5DCB2 lincRNA,lincRNA,lincRNA exon,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4286406..4286473 26863196 MeRIP-seq:(Medium) rs564371825 Functional Loss SNV dbSNP153 33..33 33 - - - 73330 RMVar_ID_73330 Human_SNP_ID_591895331 m1A Human chr16 - 4290566 4290565 4290566 GGCAGAGGGAGAAGGAGAGGGAGAGGGCTGGCAGGCGCCCATAGCTGGGGCCAGAGAGAGAGGGT GGCAGAGGGAGAAGGAGAGGGAGAGGGCTGGC_GGCGCCCATAGCTGGGGCCAGAGAGAGAGGGT CT C lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS0000D5DCB2 lincRNA,lincRNA,lincRNA exon,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4290517..4290616 26863196 MeRIP-seq:(Medium) rs1197123125 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23689138 73331 RMVar_ID_73331 Human_SNP_ID_591898028 m1A Human chr16 - 4299179 4299179 4299179 TCGGATCTGACATCTGGAGGCTGAATTCCAGGAGGAGAGAGACAGATTCCTGCAAGCAGATGCCA TCGGATCTGACATCTGGAGGCTGAATTCCAGGGGGAGAGAGACAGATTCCTGCAAGCAGATGCCA T C lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS0000D5DCB2,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4299130..4299281 26863196 MeRIP-seq:(Medium) rs1246110017 Functional Loss SNV dbSNP153 33..33 33 - - - 73332 RMVar_ID_73332 Human_SNP_ID_591900620 m1A Human chr16 - 4307425 4307425 4307425 GGTAGTCGAATTGGGAAACCGCCTCGGATGTCACATAAGCGCCCAGGGAGGACAGGGCAGGACAG GGTAGTCGAATTGGGAAACCGCCTCGGATGTCTCATAAGCGCCCAGGGAGGACAGGGCAGGACAG T A lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4,lnc-TFAP4-3:5,lnc-TFAP4-3:6,lnc-TFAP4-3:7 RNACentral:URS0000D574AE,RNACentral:URS0000D57CA6,RNACentral:URS0000D5E22E,RNACentral:URS00008BBD57,RNACentral:URS0000D5DCB2,RNACentral:URS00008B8BCD,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4307379..4307508 26863196 MeRIP-seq:(Medium) rs919947250 Functional Loss SNV dbSNP153 33..33 33 - - - 73333 RMVar_ID_73333 Human_SNP_ID_591903082 m1A Human chr16 - 4315782 4315782 4315782 GCGGGAGCCGGCGCTGGGCCGAGGGAGGGGGAAGGGAGGGCGGCGCGGCCGCGGGGAGCGGGCAC GCGGGAGCCGGCGCTGGGCCGAGGGAGGGGGAGGGGAGGGCGGCGCGGCCGCGGGGAGCGGGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4315762..4315827 26863196 MeRIP-seq:(Medium) rs1185605942 Functional Loss SNV dbSNP153 33..33 33 - - - 73334 RMVar_ID_73334 Human_SNP_ID_591903087 m1A Human chr16 - 4315789 4315789 4315789 GGGGGCGGCGGGAGCCGGCGCTGGGCCGAGGGAGGGGGAAGGGAGGGCGGCGCGGCCGCGGGGAG GGGGGCGGCGGGAGCCGGCGCTGGGCCGAGGGGGGGGGAAGGGAGGGCGGCGCGGCCGCGGGGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4315761..4315874 26863196 MeRIP-seq:(Medium) rs933443524 Functional Loss SNV dbSNP153 33..33 33 - - - 73335 RMVar_ID_73335 Human_SNP_ID_591903237 m1A Human chr16 - 4316181 4316181 4316181 GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGAGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGTGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4316086..4316227 26863410 MeRIP-seq:(Medium) rs1004465055 Functional Loss SNV dbSNP153 33..33 33 - - - 73336 RMVar_ID_73336 Human_SNP_ID_591903238 m1A Human chr16 - 4316181 4316181 4316181 GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGAGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGGGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4316086..4316227 26863410 MeRIP-seq:(Medium) rs1004465055 Functional Loss SNV dbSNP153 33..33 33 - - - 73337 RMVar_ID_73337 Human_SNP_ID_591903255 m1A Human chr16 + 4316209 4316209 4316209 CCCCTCCCCCGCTCGGCTCCCCGCGCCCCCCGACCGCCGGAGCCCGCAGCCCGGATCCCGACCGC CCCCTCCCCCGCTCGGCTCCCCGCGCCCCCCGGCCGCCGGAGCCCGCAGCCCGGATCCCGACCGC A G GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEK293T,Starvation treatment chr16:4315957..4316283;chr16:4316102..4316256;chr16:4316113..4316239 26863196,26863410 MeRIP-seq:(Medium) rs1379826359 Functional Loss SNV dbSNP153 33..33 33 - - - 73338 RMVar_ID_73338 Human_SNP_ID_591903260 m1A Human chr16 + 4316217 4316217 4316217 CCGCTCGGCTCCCCGCGCCCCCCGACCGCCGGAGCCCGCAGCCCGGATCCCGACCGCCCCCGCCG CCGCTCGGCTCCCCGCGCCCCCCGACCGCCGGGGCCCGCAGCCCGGATCCCGACCGCCCCCGCCG A G GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4316045..4316297 26863196 MeRIP-seq:(Medium) rs1173498483 Functional Loss SNV dbSNP153 33..33 33 - - - 73339 RMVar_ID_73339 Human_SNP_ID_591903265 m1A Human chr16 + 4316231 4316231 4316231 GCGCCCCCCGACCGCCGGAGCCCGCAGCCCGGATCCCGACCGCCCCCGCCGCTGAGGTAGGAAGC GCGCCCCCCGACCGCCGGAGCCCGCAGCCCGGGTCCCGACCGCCCCCGCCGCTGAGGTAGGAAGC A G GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4316051..4316274 26863196 MeRIP-seq:(Medium) rs989188228 Functional Loss SNV dbSNP153 33..33 33 - - - 73340 RMVar_ID_73340 Human_SNP_ID_591903366 m1A Human chr16 + 4316381 4316381 4316381 CTCCTCCCCCGCTCGCGTCCGCGCCCCGGGCCATTGTGAGCCCTCGCCGAGGCCCCCGCGTTCGC CTCCTCCCCCGCTCGCGTCCGCGCCCCGGGCCCTTGTGAGCCCTCGCCGAGGCCCCCGCGTTCGC A C GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4316369..4316496 26863196 MeRIP-seq:(Medium) rs1236566436 Functional Loss SNV dbSNP153 33..33 33 - - - 73341 RMVar_ID_73341 Human_SNP_ID_591903367 m1A Human chr16 + 4316381 4316381 4316381 CTCCTCCCCCGCTCGCGTCCGCGCCCCGGGCCATTGTGAGCCCTCGCCGAGGCCCCCGCGTTCGC CTCCTCCCCCGCTCGCGTCCGCGCCCCGGGCCGTTGTGAGCCCTCGCCGAGGCCCCCGCGTTCGC A G GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4316369..4316496 26863196 MeRIP-seq:(Medium) rs1236566436 Functional Loss SNV dbSNP153 33..33 33 - - - 73342 RMVar_ID_73342 Human_SNP_ID_591908382 m1A Human chr16 + 4332264 4332264 4332264 AGCTGGGAGCCCACTGCCTGCTGCCACCTCCAACTCCGGCCCCCTCACCATGCACTCCCTGGACG AGCTGGGAGCCCACTGCCTGCTGCCACCTCCAGCTCCGGCCCCCTCACCATGCACTCCCTGGACG A G GLIS2 Ensembl:ENSG00000126603 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4332188..4332481 26863196 MeRIP-seq:(Medium) rs779719940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27442752 Human_Splice_Rec_1671146 RMVar_hsa_circ_86042,RMVar_hsa_circ_125029,RMVar_hsa_circ_349101,RMVar_hsa_circ_270211,RMVar_hsa_circ_89367,RMVar_hsa_circ_175977,RMVar_hsa_circ_175979,RMVar_hsa_circ_175981,RMVar_hsa_circ_75639,RMVar_hsa_circ_175980,RMVar_hsa_circ_175978,RMVar_hsa_circ_175976,RMVar_hsa_circ_265583 73343 RMVar_ID_73343 Human_SNP_ID_591909975 m1A Human chr16 + 4336948 4336948 4336948 CACGAGCAGCAAGAGCTCCTGCAGCTGCGCCCACCCCCCAAGCCGCCACTGCCCGCCCCCGACGG CACGAGCAGCAAGAGCTCCTGCAGCTGCGCCCCCCCCCCAAGCCGCCACTGCCCGCCCCCGACGG A C GLIS2 Ensembl:ENSG00000126603 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4336897..4337015 26863196 MeRIP-seq:(Medium) rs994806881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2457903,Human_miRNA_ID_2462826,Human_miRNA_ID_2635468,Human_miRNA_ID_2638155,Human_miRNA_ID_2873762,Human_miRNA_ID_2981725 RMVar_hsa_circ_86042,RMVar_hsa_circ_175976 73344 RMVar_ID_73344 Human_SNP_ID_591909988 m1A Human chr16 + 4336955 4336955 4336955 AGCAAGAGCTCCTGCAGCTGCGCCCACCCCCCAAGCCGCCACTGCCCGCCCCCGACGGCGGCCCC AGCAAGAGCTCCTGCAGCTGCGCCCACCCCCCCAGCCGCCACTGCCCGCCCCCGACGGCGGCCCC A C GLIS2 Ensembl:ENSG00000126603 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4336905..4336970 26863196 MeRIP-seq:(Medium) rs896610296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2388559,Human_miRNA_ID_2457903,Human_miRNA_ID_2462826,Human_miRNA_ID_2635468,Human_miRNA_ID_2638155 RMVar_hsa_circ_86042,RMVar_hsa_circ_175976 73345 RMVar_ID_73345 Human_SNP_ID_591910454 m1A Human chr16 - 4337818 4337818 4337818 AGGGAGGTGCCAGGGTGGGAGAGGGAAACGGGAGGAGGTCGGGCAGGGGAAAGCCTCTCAGAAGC AGGGAGGTGCCAGGGTGGGAGAGGGAAACGGGGGGAGGTCGGGCAGGGGAAAGCCTCTCAGAAGC T C PAM16,AC012676.1 Ensembl:ENSG00000217930,Ensembl:ENSG00000262712 Protein coding,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4337722..4337886 26863196 MeRIP-seq:(Medium) rs1275493423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261390,Human_RBP_ID_5182498,Human_RBP_ID_9420479,Human_RBP_ID_17652560 73346 RMVar_ID_73346 Human_SNP_ID_591910462 m1A Human chr16 - 4337831 4337831 4337831 TGGTCACTAGGTGAGGGAGGTGCCAGGGTGGGAGAGGGAAACGGGAGGAGGTCGGGCAGGGGAAA TGGTCACTAGGTGAGGGAGGTGCCAGGGTGGGGGAGGGAAACGGGAGGAGGTCGGGCAGGGGAAA T C PAM16 Ensembl:ENSG00000217930 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4337783..4337934 26863196 MeRIP-seq:(Medium) rs1213484485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261390,Human_RBP_ID_5182498,Human_RBP_ID_9420479,Human_RBP_ID_17652560 73347 RMVar_ID_73347 Human_SNP_ID_591911302 m1A Human chr16 - 4340298 4340298 4340298 CCCCATACGTGACTGCTCGGCTCCCCCCGCCCACCCCGCCGCCTCTAATTTATAGCTTGGTAATA CCCCATACGTGACTGCTCGGCTCCCCCCGCCCCCCCCGCCGCCTCTAATTTATAGCTTGGTAATA T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs757243713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474031,Human_RBP_ID_17690327,Human_RBP_ID_17876829,Human_RBP_ID_26446808 Human_miRNA_ID_1702395,Human_miRNA_ID_1702396,Human_miRNA_ID_2146988,Human_miRNA_ID_2873765,Human_miRNA_ID_2981728,Human_miRNA_ID_2988414 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73348 RMVar_ID_73348 Human_SNP_ID_591911758 m1A Human chr16 - 4341502 4341498 4341502 GACTGAGCGATCACCCACATGTCCACACAGCCAGCCGGGCCGCAGCTGATGCCCGAGGACGCGCT GACTGAGCGATCACCCACATGTCCACACAGCC____GGGCCGCAGCTGATGCCCGAGGACGCGCT CGGCT C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4341426..4341563 26863410 MeRIP-seq:(Medium) rs777148805 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_1004477,Human_RBP_ID_4393564,Human_RBP_ID_22541221,Human_RBP_ID_22651625 Human_Splice_Rec_1671176,Human_Splice_Rec_1671182,Human_Splice_Rec_1671188,Human_Splice_Rec_1671196,Human_Splice_Rec_1671204,Human_Splice_Rec_1671214,Human_Splice_Rec_1671238,Human_Splice_Rec_1671246,Human_Splice_Rec_1671254,Human_Splice_Rec_1671260,Human_Splice_Rec_1671328,Human_Splice_Rec_1671392,Human_Splice_Rec_1671406 Human_miRNA_ID_793742,Human_miRNA_ID_793743 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_36411,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73349 RMVar_ID_73349 Human_SNP_ID_591911763 m1A Human chr16 - 4341502 4341502 4341502 GACTGAGCGATCACCCACATGTCCACACAGCCAGCCGGGCCGCAGCTGATGCCCGAGGACGCGCT GACTGAGCGATCACCCACATGTCCACACAGCCGGCCGGGCCGCAGCTGATGCCCGAGGACGCGCT T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4341426..4341563 26863410 MeRIP-seq:(Medium) rs1480895402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004477,Human_RBP_ID_4393564,Human_RBP_ID_22541221,Human_RBP_ID_22651625 Human_Splice_Rec_1671176,Human_Splice_Rec_1671182,Human_Splice_Rec_1671188,Human_Splice_Rec_1671196,Human_Splice_Rec_1671204,Human_Splice_Rec_1671214,Human_Splice_Rec_1671238,Human_Splice_Rec_1671246,Human_Splice_Rec_1671254,Human_Splice_Rec_1671260,Human_Splice_Rec_1671328,Human_Splice_Rec_1671392,Human_Splice_Rec_1671406 Human_miRNA_ID_793742,Human_miRNA_ID_793743 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_36411,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73350 RMVar_ID_73350 Human_SNP_ID_591912361 m1A Human chr16 - 4343203 4343203 4343203 TGCACGGGCCTTGCGGCAGGAGTTTGCAGGTAAGCATGGGTCCGTCTCCCCTGTGGGCTGGGAGT TGCACGGGCCTTGCGGCAGGAGTTTGCAGGTAGGCATGGGTCCGTCTCCCCTGTGGGCTGGGAGT T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4343201..4343250 26863196 MeRIP-seq:(Medium) rs375267596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4369129,Human_RBP_ID_5357545,Human_RBP_ID_19070755 Human_Splice_Rec_1671174,Human_Splice_Rec_1671194,Human_Splice_Rec_1671202,Human_Splice_Rec_1671212,Human_Splice_Rec_1671220,Human_Splice_Rec_1671228,Human_Splice_Rec_1671236,Human_Splice_Rec_1671244,Human_Splice_Rec_1671252,Human_Splice_Rec_1671266,Human_Splice_Rec_1671326,Human_Splice_Rec_1671390 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_36411,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73351 RMVar_ID_73351 Human_SNP_ID_591912362 m1A Human chr16 - 4343203 4343203 4343203 TGCACGGGCCTTGCGGCAGGAGTTTGCAGGTAAGCATGGGTCCGTCTCCCCTGTGGGCTGGGAGT TGCACGGGCCTTGCGGCAGGAGTTTGCAGGTACGCATGGGTCCGTCTCCCCTGTGGGCTGGGAGT T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4343201..4343250 26863196 MeRIP-seq:(Medium) rs375267596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4369129,Human_RBP_ID_5357545,Human_RBP_ID_19070755 Human_Splice_Rec_1671174,Human_Splice_Rec_1671194,Human_Splice_Rec_1671202,Human_Splice_Rec_1671212,Human_Splice_Rec_1671220,Human_Splice_Rec_1671228,Human_Splice_Rec_1671236,Human_Splice_Rec_1671244,Human_Splice_Rec_1671252,Human_Splice_Rec_1671266,Human_Splice_Rec_1671326,Human_Splice_Rec_1671390 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_36411,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73352 RMVar_ID_73352 Human_SNP_ID_591912814 m1A Human chr16 - 4344384 4344333 4344385 TCCTCTCACAGAACCCCCTCCTCTCACACAGAACCCCCTCCTCTCACACAGAACCCCCTCTTCTC TCCTCTCACAGAACCCCCTCCTCTCACACAG__________________________________ AGAGGAGGGGGTTCTGTGTGAGAAGAGGGGGTTCTGTGTGAGAGGAGGGGGTT A PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4344378..4344628 26863196 MeRIP-seq:(Medium) rs1567230988 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_2474713,Human_RBP_ID_9842731,Human_RBP_ID_22939347,Human_RBP_ID_25244481 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73353 RMVar_ID_73353 Human_SNP_ID_591912846 m1A Human chr16 - 4344384 4344382 4344384 TCCTCTCACAGAACCCCCTCCTCTCACACAGAACCCCCTCCTCTCACACAGAACCCCCTCTTCTC TCCTCTCACAGAACCCCCTCCTCTCACACAGA__CCCCTCCTCTCACACAGAACCCCCTCTTCTC GGT G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4344378..4344628 26863196 MeRIP-seq:(Medium) rs1458304401 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2474713,Human_RBP_ID_9842731,Human_RBP_ID_22939347,Human_RBP_ID_25244481 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73354 RMVar_ID_73354 Human_SNP_ID_591912848 m1A Human chr16 - 4344384 4344383 4344385 TCCTCTCACAGAACCCCCTCCTCTCACACAGAACCCCCTCCTCTCACACAGAACCCCCTCTTCTC TCCTCTCACAGAACCCCCTCCTCTCACACAG__CCCCCTCCTCTCACACAGAACCCCCTCTTCTC GTT G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4344378..4344628 26863196 MeRIP-seq:(Medium) rs1436141678 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2474713,Human_RBP_ID_9842731,Human_RBP_ID_22939347,Human_RBP_ID_25244481 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73355 RMVar_ID_73355 Human_SNP_ID_591912851 m1A Human chr16 - 4344384 4344384 4344384 TCCTCTCACAGAACCCCCTCCTCTCACACAGAACCCCCTCCTCTCACACAGAACCCCCTCTTCTC TCCTCTCACAGAACCCCCTCCTCTCACACAGACCCCCCTCCTCTCACACAGAACCCCCTCTTCTC T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4344378..4344628 26863196 MeRIP-seq:(Medium) rs1375692007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2474713,Human_RBP_ID_9842731,Human_RBP_ID_22939347,Human_RBP_ID_25244481 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73356 RMVar_ID_73356 Human_SNP_ID_591912882 m1A Human chr16 - 4344531 4344478 4344532 CCCTCCTCTCACGGAACCCCCTCCTCTCACACAGTCCCCTTCTCTCACAGAACCCCCTCCTCTCA CCCTCCTCTCACGGAACCCCCTCCTCTCACA__________________________________ CTGTGAGAGGAGGGGGTTCTGTGAGAGGAGGGGGTTCTGTGAGAGAAGGGGACTG C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:4344492..4344621 26863196 MeRIP-seq:(Medium) rs1567231115 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_5128034,Human_RBP_ID_17077343,Human_RBP_ID_18938726,Human_RBP_ID_24551880,Human_RBP_ID_26441211 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73357 RMVar_ID_73357 Human_SNP_ID_591913030 m1A Human chr16 + 4344755 4344740 4344755 GGTTCCGTGAGAGGAGGGGGTTCTGTGAGAGGAGGGGGTTCCGTGAGAGGAGGGGGTTCTGTGAG GGTTCCGTGAGAGGAGGG_______________GGGGGTTCCGTGAGAGGAGGGGGTTCTGTGAG GGGTTCTGTGAGAGGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4344753..4344858 26863196 MeRIP-seq:(Medium) rs1374831376 Functional Loss DEL dbSNP153 19..33 33 - - - 73358 RMVar_ID_73358 Human_SNP_ID_591913038 m1A Human chr16 + 4344755 4344755 4344755 GGTTCCGTGAGAGGAGGGGGTTCTGTGAGAGGAGGGGGTTCCGTGAGAGGAGGGGGTTCTGTGAG GGTTCCGTGAGAGGAGGGGGTTCTGTGAGAGGGGGGGGTTCCGTGAGAGGAGGGGGTTCTGTGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4344753..4344858 26863196 MeRIP-seq:(Medium) rs1321375165 Functional Loss SNV dbSNP153 33..33 33 - - - 73359 RMVar_ID_73359 Human_SNP_ID_591913040 m1A Human chr16 - 4344761 4344761 4344761 CCTCCTCTCACAGAACCCCCTCCTCTCACGGAACCCCCTCCTCTCACAGAACCCCCTCCTCTCAC CCTCCTCTCACAGAACCCCCTCCTCTCACGGAGCCCCCTCCTCTCACAGAACCCCCTCCTCTCAC T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4344754..4344911 26863196 MeRIP-seq:(Medium) rs1432975086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73360 RMVar_ID_73360 Human_SNP_ID_591914137 m1A Human chr16 + 4348259 4348259 4348259 TCTGAATGAATATGGCTGTTGCAGCTTTGCCCAATCTGCTGTCTCATGAACTCCATGTCCCCAGG TCTGAATGAATATGGCTGTTGCAGCTTTGCCCCATCTGCTGTCTCATGAACTCCATGTCCCCAGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4348256..4348599 26863196 MeRIP-seq:(Medium) rs1344988540 Functional Loss SNV dbSNP153 33..33 33 - - - 73361 RMVar_ID_73361 Human_SNP_ID_591915188 m1A Human chr16 - 4351058 4351049 4351058 CACCCGGGGGAATCGAGGCCGGCAGCGGCGGCACCGGCGGCCTCAGGGCCAGGGAAAACCGTCTG CACCCGGGGGAATCGAGGCCGGCAGCGGCGGC_________CTCAGGGCCAGGGAAAACCGTCTG GGCCGCCGGT G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4351052..4351330 26863196 MeRIP-seq:(Medium) rs967937459 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_261392,Human_RBP_ID_3502493,Human_RBP_ID_5316553,Human_RBP_ID_5356440,Human_RBP_ID_8084735,Human_RBP_ID_8231237,Human_RBP_ID_8726114,Human_RBP_ID_9324914,Human_RBP_ID_18418651,Human_RBP_ID_18482129,Human_RBP_ID_19075851,Human_RBP_ID_21972993,Human_RBP_ID_22474353,Human_RBP_ID_26780149 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73362 RMVar_ID_73362 Human_SNP_ID_591915205 m1A Human chr16 - 4351079 4351079 4351079 AAGCATGGTCTGGGGGCGTTGCACCCGGGGGAATCGAGGCCGGCAGCGGCGGCACCGGCGGCCTC AAGCATGGTCTGGGGGCGTTGCACCCGGGGGAGTCGAGGCCGGCAGCGGCGGCACCGGCGGCCTC T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:4351076..4351208 26863196 MeRIP-seq:(Medium) rs1010554956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261392,Human_RBP_ID_474061,Human_RBP_ID_3502493,Human_RBP_ID_5316553,Human_RBP_ID_5355607,Human_RBP_ID_8084735,Human_RBP_ID_8231237,Human_RBP_ID_8726114,Human_RBP_ID_9324914,Human_RBP_ID_18418651,Human_RBP_ID_18482129,Human_RBP_ID_19075851,Human_RBP_ID_21972993,Human_RBP_ID_22474353,Human_RBP_ID_24552060,Human_RBP_ID_26780149 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 73363 RMVar_ID_73363 Human_SNP_ID_591920410 m1A Human chr16 + 4364920 4364920 4364920 CACGCAGCACGCTCTCCAGGACACACTGGGTCACTGTTGAGGACACCATAGGGGAACAGGCAGGA CACGCAGCACGCTCTCCAGGACACACTGGGTCGCTGTTGAGGACACCATAGGGGAACAGGCAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4364873..4387804 32194978 MeRIP-seq:(Medium) rs1479544887 Functional Loss SNV dbSNP153 33..33 33 - - - 73364 RMVar_ID_73364 Human_SNP_ID_591922517 m1A Human chr16 + 4371894 4371882 4371894 AGCCCGGGGCGGGTGGACGCGGACTCGAACGCAGTTGCTTCGGGACCCAGGACCCCCTCGGGCCC AGCCCGGGGCGGGTGGACGCG____________GTTGCTTCGGGACCCAGGACCCCCTCGGGCCC GGACTCGAACGCA G VASN Ensembl:ENSG00000168140 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4371851..4372041 26863196 MeRIP-seq:(Medium) rs1388704858 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4392831,Human_RBP_ID_18418653,Human_RBP_ID_23128358 Human_Splice_Rec_1671961 73365 RMVar_ID_73365 Human_SNP_ID_591922544 m1A Human chr16 + 4371946 4371946 4371946 CCCCCTCGGGCCCGACCCGCCAGGAAAGACTGAGGCCGCGGCCTGCCCCGCCCGGCTCCCTGCGC CCCCCTCGGGCCCGACCCGCCAGGAAAGACTGGGGCCGCGGCCTGCCCCGCCCGGCTCCCTGCGC A G VASN Ensembl:ENSG00000168140 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:4371901..4371991;chr16:4371899..4372093;chr16:4371896..4371993 26863196 MeRIP-seq:(Medium) rs1424113678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392832 Human_Splice_Rec_1671961 73366 RMVar_ID_73366 Human_SNP_ID_591926377 m1A Human chr16 + 4383272 4383272 4383272 CCTGGGGGCCAGTGAAGGAAGCTCCCGGAAAGAGCAGAGGGAGAGCGGGTAGGCGGCTGTGTGAC CCTGGGGGCCAGTGAAGGAAGCTCCCGGAAAGTGCAGAGGGAGAGCGGGTAGGCGGCTGTGTGAC A T VASN Ensembl:ENSG00000168140 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4383223..4383302 26863196 MeRIP-seq:(Medium) rs1295072777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445760 73367 RMVar_ID_73367 Human_SNP_ID_591927933 m1A Human chr16 - 4388550 4388550 4388550 GCACCTGGGAGCACCTTGTGTCTACTGGATTCAACCAGGTAGGGGGTTCCTCCTGGAGGAGCAGG GCACCTGGGAGCACCTTGTGTCTACTGGATTCGACCAGGTAGGGGGTTCCTCCTGGAGGAGCAGG T C CORO7,CORO7-PAM16 Ensembl:ENSG00000262246,Ensembl:ENSG00000103426 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4388002..4388579 32194978 MeRIP-seq:(Medium) rs750253888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889401,Human_RBP_ID_3947226,Human_RBP_ID_18983115,Human_RBP_ID_22944593,Human_RBP_ID_23118574,Human_RBP_ID_26328596 Human_Splice_Rec_1671286,Human_Splice_Rec_1671287,Human_Splice_Rec_1671348,Human_Splice_Rec_1671349,Human_Splice_Rec_1671422,Human_Splice_Rec_1671423,Human_Splice_Rec_1671478,Human_Splice_Rec_1671479,Human_Splice_Rec_1671532,Human_Splice_Rec_1671533,Human_Splice_Rec_1671582,Human_Splice_Rec_1671583,Human_Splice_Rec_1671666,Human_Splice_Rec_1671667,Human_Splice_Rec_1671722,Human_Splice_Rec_1671723,Human_Splice_Rec_1671784,Human_Splice_Rec_1671785,Human_Splice_Rec_1671804,Human_Splice_Rec_1671805,Human_Splice_Rec_1671818,Human_Splice_Rec_1671819,Human_Splice_Rec_1671828,Human_Splice_Rec_1671829,Human_Splice_Rec_1671839,Human_Splice_Rec_1671850,Human_Splice_Rec_1671866,Human_Splice_Rec_1671874 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_96482,RMVar_hsa_circ_98927,RMVar_hsa_circ_175986,RMVar_hsa_circ_175987,RMVar_hsa_circ_119205,RMVar_hsa_circ_268144,RMVar_hsa_circ_267640,RMVar_hsa_circ_175994 73368 RMVar_ID_73368 Human_SNP_ID_591935857 m1A Human chr16 + 4413404 4413404 4413404 GGCGGTTCCTGCTCGAATGTCACTGATCCAGGACTGAAAATCAAGAGTAAAGAAGTATGTGGTGA GGCGGTTCCTGCTCGAATGTCACTGATCCAGGGCTGAAAATCAAGAGTAAAGAAGTATGTGGTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4413369..4416577 26863196 MeRIP-seq:(Medium) rs1317966795 Functional Loss SNV dbSNP153 33..33 33 - - - 73369 RMVar_ID_73369 Human_SNP_ID_591936889 m1A Human chr16 + 4416477 4416477 4416477 CGGGCCGGACTCACCTCGCGGCGGGGCGGCCGAGCCTCGGTGTGCCGGAACTTGGACACCCTGAA CGGGCCGGACTCACCTCGCGGCGGGGCGGCCGGGCCTCGGTGTGCCGGAACTTGGACACCCTGAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4416460..4416561 32194978 MeRIP-seq:(Medium) rs774784230 Functional Loss SNV dbSNP153 33..33 33 - - - 73370 RMVar_ID_73370 Human_SNP_ID_591936949 m1A Human chr16 - 4416563 4416563 4416563 GTCGCGGTTGCTCAGCGTGCACCTGAGACCCGACGCCCGGGGTCCTCGAAGACGCGTCCGCCGCC GTCGCGGTTGCTCAGCGTGCACCTGAGACCCGGCGCCCGGGGTCCTCGAAGACGCGTCCGCCGCC T C CORO7,CORO7-PAM16 Ensembl:ENSG00000262246,Ensembl:ENSG00000103426 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4416400..4416595 26863196 MeRIP-seq:(Medium) rs1023219251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393568,Human_RBP_ID_9285626 Human_Splice_Rec_1671852 73371 RMVar_ID_73371 Human_SNP_ID_591940148 m1A Human chr16 + 4425956 4425956 4425956 GGGACCCCGCGGCTGCCGGCTATATCGGGTAGAGGGGCCCGGCCGCCCAGGGAGGGCGTGGTGGG GGGACCCCGCGGCTGCCGGCTATATCGGGTAGTGGGGCCCGGCCGCCCAGGGAGGGCGTGGTGGG A T DNAJA3 Ensembl:ENSG00000103423 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4425910..4426027 26863196 MeRIP-seq:(Medium) rs1047717308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4369244,Human_RBP_ID_9324919,Human_RBP_ID_22441744 73372 RMVar_ID_73372 Human_SNP_ID_591940200 m1A Human chr16 + 4426055 4426055 4426055 TTTGCGTCTTCCCTGACCTCTTGCGGCCCCCGAGCGCTGCTGACATTGAGACCTGGTGTCAGCCT TTTGCGTCTTCCCTGACCTCTTGCGGCCCCCGGGCGCTGCTGACATTGAGACCTGGTGTCAGCCT A G DNAJA3 Ensembl:ENSG00000103423 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:4425901..4431660 32194978 MeRIP-seq:(Medium) rs1405363983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474079,Human_RBP_ID_4393571,Human_RBP_ID_9325844,Human_RBP_ID_12736574,Human_RBP_ID_18679415,Human_RBP_ID_22202283,Human_RBP_ID_22441744,Human_RBP_ID_23689222 Human_Splice_Rec_1671963,Human_Splice_Rec_1671979,Human_Splice_Rec_1671999,Human_Splice_Rec_1672005,Human_Splice_Rec_1672015,Human_Splice_Rec_1672031,Human_Splice_Rec_1672033,Human_Splice_Rec_1672055,Human_Splice_Rec_1672061 73373 RMVar_ID_73373 Human_SNP_ID_591947087 m1A Human chr16 + 4447000 4447000 4447000 GGGGTACAGCCAGAGCCCAGGGCCTGTACGAGACGATCAACGTGACGGTAAGAGGGTGTGAGAAC GGGGTACAGCCAGAGCCCAGGGCCTGTACGAGGCGATCAACGTGACGGTAAGAGGGTGTGAGAAC A G DNAJA3 Ensembl:ENSG00000103423 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:4446976..4447000 32194978 MeRIP-seq:(Medium) rs1414936201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818038,Human_RBP_ID_895346,Human_RBP_ID_1178161,Human_RBP_ID_1518380,Human_RBP_ID_12737178,Human_RBP_ID_19073191 Human_Splice_Rec_1671973,Human_Splice_Rec_1671993,Human_Splice_Rec_1672025,Human_Splice_Rec_1672047 RMVar_hsa_circ_175999,RMVar_hsa_circ_369834,RMVar_hsa_circ_376232,RMVar_hsa_circ_126401,RMVar_hsa_circ_50005,RMVar_hsa_circ_175998,RMVar_hsa_circ_176004,RMVar_hsa_circ_374708,RMVar_hsa_circ_176002,RMVar_hsa_circ_340550,RMVar_hsa_circ_176003 73374 RMVar_ID_73374 Human_SNP_ID_591948425 m1A Human chr16 + 4450474 4450474 4450474 CGAGGACGAGACAGATGTGGAGGGGACGGTGAACGGCGTCACCCTCACCAGCTCTGGTAAGGAGT CGAGGACGAGACAGATGTGGAGGGGACGGTGAGCGGCGTCACCCTCACCAGCTCTGGTAAGGAGT A G DNAJA3 Ensembl:ENSG00000103423 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:4450451..4450475 32194978 MeRIP-seq:(Medium) rs750709373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233503,Human_RBP_ID_474123,Human_RBP_ID_818041,Human_RBP_ID_894087,Human_RBP_ID_5113355,Human_RBP_ID_9372184,Human_RBP_ID_17876886,Human_RBP_ID_19073194 Human_Splice_Rec_1671976,Human_Splice_Rec_1671977,Human_Splice_Rec_1671996,Human_Splice_Rec_1671997,Human_Splice_Rec_1672028,Human_Splice_Rec_1672029,Human_Splice_Rec_1672050,Human_Splice_Rec_1672051,Human_Splice_Rec_1672081 Human_miRNA_ID_2052213 RMVar_hsa_circ_369834,RMVar_hsa_circ_126401,RMVar_hsa_circ_175998,RMVar_hsa_circ_176004,RMVar_hsa_circ_176002,RMVar_hsa_circ_340550,RMVar_hsa_circ_176005,RMVar_hsa_circ_290180,RMVar_hsa_circ_176006,RMVar_hsa_circ_378017 73375 RMVar_ID_73375 Human_SNP_ID_591949992 m1A Human chr16 + 4455655 4455655 4455655 CCAGAACAGCAGCACTGAGCTCCCACCCGCAGAGCCTCTGGACGGCCTTGGCAACAGCAAAATCA CCAGAACAGCAGCACTGAGCTCCCACCCGCAGCGCCTCTGGACGGCCTTGGCAACAGCAAAATCA A C DNAJA3 Ensembl:ENSG00000103423 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4455607..4455686 26863196 MeRIP-seq:(Medium) rs1027918803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233504,Human_RBP_ID_474140,Human_RBP_ID_6513212,Human_RBP_ID_9372185,Human_RBP_ID_12737446 Human_miRNA_ID_1395167,Human_miRNA_ID_2395833,Human_miRNA_ID_2825615,Human_miRNA_ID_2859586,Human_miRNA_ID_3069624 RMVar_hsa_circ_176006,RMVar_hsa_circ_378017 73376 RMVar_ID_73376 Human_SNP_ID_591949993 m1A Human chr16 + 4455655 4455655 4455655 CCAGAACAGCAGCACTGAGCTCCCACCCGCAGAGCCTCTGGACGGCCTTGGCAACAGCAAAATCA CCAGAACAGCAGCACTGAGCTCCCACCCGCAGGGCCTCTGGACGGCCTTGGCAACAGCAAAATCA A G DNAJA3 Ensembl:ENSG00000103423 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4455607..4455686 26863196 MeRIP-seq:(Medium) rs1027918803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233504,Human_RBP_ID_474140,Human_RBP_ID_6513212,Human_RBP_ID_9372185,Human_RBP_ID_12737446 Human_miRNA_ID_1395167,Human_miRNA_ID_2395833,Human_miRNA_ID_2825615,Human_miRNA_ID_2859586,Human_miRNA_ID_3069624 RMVar_hsa_circ_176006,RMVar_hsa_circ_378017 73377 RMVar_ID_73377 Human_SNP_ID_591951779 m1A Human chr16 + 4461818 4461818 4461818 CAGGTTGAAGTCCCCTTTGTGCTGTTCCAGCCACTGGTCCAGCGTCAGGGCCTTGGGGTTGAGTC CAGGTTGAAGTCCCCTTTGTGCTGTTCCAGCCCCTGGTCCAGCGTCAGGGCCTTGGGGTTGAGTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4461767..4461904 26863196 MeRIP-seq:(Medium) rs748351440 Functional Loss SNV dbSNP153 33..33 33 - - - 73378 RMVar_ID_73378 Human_SNP_ID_591951826 m1A Human chr16 + 4461901 4461901 4461901 CACGGTCGGGTCTCAGGGCATAGAAACGGAACATGTTGGCCAGGTCCCGGGCACCGGGAAAGCCA CACGGTCGGGTCTCAGGGCATAGAAACGGAACGTGTTGGCCAGGTCCCGGGCACCGGGAAAGCCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:4461729..4463439 32194978 MeRIP-seq:(Medium) rs1474293855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12737579 73379 RMVar_ID_73379 Human_SNP_ID_591952423 m1A Human chr16 - 4463692 4463692 4463692 ACACGGCCGAGGAGTACGCTGCCCTGCTCACCAAGCACACCCGCAAGGTCGTGCACGATGCCAAG ACACGGCCGAGGAGTACGCTGCCCTGCTCACCGAGCACACCCGCAAGGTCGTGCACGATGCCAAG T C NMRAL1 Ensembl:ENSG00000153406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4463681..4463790 26863196 MeRIP-seq:(Medium) rs767966409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373732,Human_RBP_ID_26445773 Human_Splice_Rec_1672095,Human_Splice_Rec_1672105,Human_Splice_Rec_1672109,Human_Splice_Rec_1672113,Human_Splice_Rec_1672123,Human_Splice_Rec_1672133,Human_Splice_Rec_1672137,Human_Splice_Rec_1672139 Human_miRNA_ID_2237452 RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_342548,RMVar_hsa_circ_369689,RMVar_hsa_circ_176012 73380 RMVar_ID_73380 Human_SNP_ID_591952450 m1A Human chr16 + 4463739 4463739 4463739 CGTACTCCTCGGCCGTGTGCCTGCAAGTGCTCAGCCCGATGTTCTGGCCGACGTATTTTTCTGGC CGTACTCCTCGGCCGTGTGCCTGCAAGTGCTCGGCCCGATGTTCTGGCCGACGTATTTTTCTGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4463593..4463943 32194978 MeRIP-seq:(Medium) rs759598693 Functional Loss SNV dbSNP153 33..33 33 - - - 73381 RMVar_ID_73381 Human_SNP_ID_591952460 m1A Human chr16 - 4463751 4463751 4463751 CCTTTTGAAGATGCCAGAAAAATACGTCGGCCAGAACATCGGGCTGAGCACTTGCAGGCACACGG CCTTTTGAAGATGCCAGAAAAATACGTCGGCCGGAACATCGGGCTGAGCACTTGCAGGCACACGG T C NMRAL1 Ensembl:ENSG00000153406 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4463702..4463795 26863196 MeRIP-seq:(Medium) rs747435820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373732,Human_RBP_ID_26445773 Human_Splice_Rec_1672094,Human_Splice_Rec_1672095,Human_Splice_Rec_1672104,Human_Splice_Rec_1672105,Human_Splice_Rec_1672108,Human_Splice_Rec_1672109,Human_Splice_Rec_1672112,Human_Splice_Rec_1672122,Human_Splice_Rec_1672123,Human_Splice_Rec_1672132,Human_Splice_Rec_1672133,Human_Splice_Rec_1672136,Human_Splice_Rec_1672137,Human_Splice_Rec_1672139,Human_Splice_Rec_1672144,Human_Splice_Rec_1672154,Human_Splice_Rec_1672160 Human_miRNA_ID_2316433,Human_miRNA_ID_2319589,Human_miRNA_ID_2322746,Human_miRNA_ID_2325919,Human_miRNA_ID_2520296,Human_miRNA_ID_2523458,Human_miRNA_ID_2822658,Human_miRNA_ID_2831940 RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_342548,RMVar_hsa_circ_369689,RMVar_hsa_circ_176012 73382 RMVar_ID_73382 Human_SNP_ID_591954301 m1A Human chr16 - 4469277 4469277 4469277 AGCTGGCCCTGAATGGGGCTTACGCCACCTTCATCGTGACCAATTACTGGGAGAGCTGCAGCCAG AGCTGGCCCTGAATGGGGCTTACGCCACCTTCGTCGTGACCAATTACTGGGAGAGCTGCAGCCAG T C NMRAL1 Ensembl:ENSG00000153406 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4469226..4469387 32194978 MeRIP-seq:(Medium) rs1555491989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5114408,Human_RBP_ID_5495711 Human_Splice_Rec_1672091,Human_Splice_Rec_1672101,Human_Splice_Rec_1672119,Human_Splice_Rec_1672129,Human_Splice_Rec_1672141,Human_Splice_Rec_1672167,Human_Splice_Rec_1672173,Human_Splice_Rec_1672179 Human_miRNA_ID_340894 RMVar_hsa_circ_58907,RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_342548,RMVar_hsa_circ_369689,RMVar_hsa_circ_176012,RMVar_hsa_circ_176014,RMVar_hsa_circ_271861 73383 RMVar_ID_73383 Human_SNP_ID_591954355 m1A Human chr16 - 4469377 4469376 4469377 CGAGTGGTGACCCGAAACCCTAGGAAGAAGGCAGCAAAGGAGCTGAGGCTGCAAGGTGCAGAAGT CGAGTGGTGACCCGAAACCCTAGGAAGAAGGC_GCAAAGGAGCTGAGGCTGCAAGGTGCAGAAGT CT C NMRAL1 Ensembl:ENSG00000153406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4469182..4469499 26863196 MeRIP-seq:(Medium) rs1567357651 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1672090,Human_Splice_Rec_1672100,Human_Splice_Rec_1672118,Human_Splice_Rec_1672128,Human_Splice_Rec_1672166,Human_Splice_Rec_1672178,Human_Splice_Rec_1672186,Human_Splice_Rec_1672192 RMVar_hsa_circ_58907,RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_342548,RMVar_hsa_circ_369689,RMVar_hsa_circ_176012,RMVar_hsa_circ_176014,RMVar_hsa_circ_271861 73384 RMVar_ID_73384 Human_SNP_ID_591956001 m1A Human chr16 - 4474209 4474204 4474210 AATGGGGGTGTCCTTTGTCGCTCCTGGCGGGAACCCCGGCCCCACCCCCAACTCCACGCCTCCCA AATGGGGGTGTCCTTTGTCGCTCCTGGCGGG______GGCCCCACCCCCAACTCCACGCCTCCCA CGGGGTT C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:4474205..4474379;chr16:4474204..4474317 26863196 MeRIP-seq:(Medium) rs1375219879 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_22653852 RMVar_hsa_circ_108642,RMVar_hsa_circ_176010,RMVar_hsa_circ_57885 73385 RMVar_ID_73385 Human_SNP_ID_591956117 m1A Human chr16 - 4474491 4474491 4474491 CGCCTAGCGCGCAGCTCCATCCCCGCCTCTGCAGTGGACTCGGCCGCAGAATCGGGGTCCCGGGC CGCCTAGCGCGCAGCTCCATCCCCGCCTCTGCGGTGGACTCGGCCGCAGAATCGGGGTCCCGGGC T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:4474205..4474625;chr16:4474451..4474584 26863196 MeRIP-seq:(Medium) rs954477071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393576,Human_RBP_ID_9324921,Human_RBP_ID_23689301 Human_Splice_Rec_1672115,Human_Splice_Rec_1672125,Human_Splice_Rec_1672169,Human_Splice_Rec_1672181,Human_Splice_Rec_1672187,Human_Splice_Rec_1672193 RMVar_hsa_circ_108642,RMVar_hsa_circ_176010,RMVar_hsa_circ_57885 73386 RMVar_ID_73386 Human_SNP_ID_591956769 m1A Human chr16 + 4476471 4476471 4476471 GGGCACGCTGACTGGAGGCTGGCGGACAGGCGACAGCGACCTGCGGCAGGTGAGCTGTCCGCGCC GGGCACGCTGACTGGAGGCTGGCGGACAGGCGGCAGCGACCTGCGGCAGGTGAGCTGTCCGCGCC A G HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4476401..4476532 26863196 MeRIP-seq:(Medium) rs1367775114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393577,Human_RBP_ID_20167491 Human_Splice_Rec_1672223,Human_Splice_Rec_1672235,Human_Splice_Rec_1672265,Human_Splice_Rec_1672275,Human_Splice_Rec_1672283,Human_Splice_Rec_1672297,Human_Splice_Rec_1672305,Human_Splice_Rec_1672311 73387 RMVar_ID_73387 Human_SNP_ID_591959141 m1A Human chr16 - 4483675 4483675 4483675 TCCGGGAAGCGGAGGTTGCAGTGAGCCGAGATAGCGCCATTGCACTCCAGCCTGGGTGTCGCAGC TCCGGGAAGCGGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGTGTCGCAGC T G NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4483672..4483754 26863196 MeRIP-seq:(Medium) rs1292104806 Functional Loss SNV dbSNP153 33..33 33 - - - 73388 RMVar_ID_73388 Human_SNP_ID_591965507 m1A Human chr16 - 4506863 4506863 4506863 TCTGTGGAGAGATGGGAGGTGTTTGTGTGTCAATTAGCCCTTCCCAGCTTTCCAGAAAGGACCAT TCTGTGGAGAGATGGGAGGTGTTTGTGTGTCAGTTAGCCCTTCCCAGCTTTCCAGAAAGGACCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4506861..4506975 26863196 MeRIP-seq:(Medium) rs775285965 Functional Loss SNV dbSNP153 33..33 33 - - - 73389 RMVar_ID_73389 Human_SNP_ID_591967054 m1A Human chr16 - 4511830 4511830 4511830 TTTGAGTCAGTGTGCAGACCCCCTTTCAGGCCATGCCTCTGTGAACCCTGTATTGCTGGGGCCGG TTTGAGTCAGTGTGCAGACCCCCTTTCAGGCCTTGCCTCTGTGAACCCTGTATTGCTGGGGCCGG T A CDIP1 Ensembl:ENSG00000089486 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4511369..4511965 32194978 MeRIP-seq:(Medium) rs1025616830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066214,Human_RBP_ID_5113360,Human_RBP_ID_5128490 Human_miRNA_ID_1061712 73390 RMVar_ID_73390 Human_SNP_ID_591967213 m1A Human chr16 + 4512504 4512504 4512504 TCCCAGCCCCAAGTGGGAGCGGGAAAGTGACCACTGAGCACAGGGAGCAAAGCACAGGGGGCCAG TCCCAGCCCCAAGTGGGAGCGGGAAAGTGACCTCTGAGCACAGGGAGCAAAGCACAGGGGGCCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4512453..4512569 26863196 MeRIP-seq:(Medium) rs887358512 Functional Loss SNV dbSNP153 33..33 33 - - - 73391 RMVar_ID_73391 Human_SNP_ID_591967806 m1A Human chr16 + 4514078 4514078 4514078 CTGGGGTGGGCGGGGCTCCACTTTTCTCTTCCAGAAGTGGGGCTGTGGGGCCCCCAGGATAAGGA CTGGGGTGGGCGGGGCTCCACTTTTCTCTTCCGGAAGTGGGGCTGTGGGGCCCCCAGGATAAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4513742..4514085 32194978 MeRIP-seq:(Medium) rs368271407 Functional Loss SNV dbSNP153 33..33 33 - - - 73392 RMVar_ID_73392 Human_SNP_ID_591973996 m1A Human chr16 - 4536006 4536006 4536006 TGGGGAGGATGGAGAGAGAGAGCCAGGCCGGCAGTGGTGACAGGAGGTTCCCTTTCCCCCACGAG TGGGGAGGATGGAGAGAGAGAGCCAGGCCGGCCGTGGTGACAGGAGGTTCCCTTTCCCCCACGAG T G CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4536005..4536133 26863196 MeRIP-seq:(Medium) rs1285221298 Functional Loss SNV dbSNP153 33..33 33 - - - 73393 RMVar_ID_73393 Human_SNP_ID_591996862 m1A Human chr16 + 4609081 4609079 4609081 AACGCTGGCTGACGAGGGGGTGGGGAGGAGGCAGGGCCCTGGGGAGGGGGCGGCGGGCAGGGGGC AACGCTGGCTGACGAGGGGGTGGGGAGGAGG__GGGCCCTGGGGAGGGGGCGGCGGGCAGGGGGC GCA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:4609034..4609194 26863196 MeRIP-seq:(Medium) rs1348484454 Functional Loss DEL dbSNP153 32..33 33 - - - 73394 RMVar_ID_73394 Human_SNP_ID_591996874 m1A Human chr16 + 4609093 4609093 4609093 CGAGGGGGTGGGGAGGAGGCAGGGCCCTGGGGAGGGGGCGGCGGGCAGGGGGCTGGGGGCTCACA CGAGGGGGTGGGGAGGAGGCAGGGCCCTGGGGGGGGGGCGGCGGGCAGGGGGCTGGGGGCTCACA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4609001..4609175 26863410 MeRIP-seq:(Medium) rs980063398 Functional Loss SNV dbSNP153 33..33 33 - - - 73395 RMVar_ID_73395 Human_SNP_ID_591998124 m1A Human chr16 - 4612500 4612500 4612500 AGCCTGGGCTTTGGGGCACAGCTGCTGCTGACAGAGGGTCTTGGGGTCTGGGAAGGTGCTTAAAG AGCCTGGGCTTTGGGGCACAGCTGCTGCTGACGGAGGGTCTTGGGGTCTGGGAAGGTGCTTAAAG T C UBALD1 Ensembl:ENSG00000153443 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4612498..4612897 26863196 MeRIP-seq:(Medium) rs1182108030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763735,Human_RBP_ID_3502510,Human_RBP_ID_5181845,Human_RBP_ID_5237216,Human_RBP_ID_6513463,Human_RBP_ID_8084764,Human_RBP_ID_8726124,Human_RBP_ID_12738479,Human_RBP_ID_18418655,Human_RBP_ID_18458367,Human_RBP_ID_18482143,Human_RBP_ID_22054453,Human_RBP_ID_22714252,Human_RBP_ID_26779173 73396 RMVar_ID_73396 Human_SNP_ID_591998342 m1A Human chr16 + 4613255 4613255 4613255 GGAGCTTCCTCCGGGTGGGGCTGCCTTGGGGCACAGGGGGCAGTAAGCTGGCCAACAGAAGCTGA GGAGCTTCCTCCGGGTGGGGCTGCCTTGGGGCTCAGGGGGCAGTAAGCTGGCCAACAGAAGCTGA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4613222..4613324 32194978 MeRIP-seq:(Medium) rs568527248 Functional Loss SNV dbSNP153 33..33 33 - - - 73397 RMVar_ID_73397 Human_SNP_ID_591998943 m1A Human chr16 - 4614829 4614826 4614829 GTGGACGCGTGAGGCGGAGGCGCGGGCGGAGGAGGGAGGCCGGAGCGGGCAGCGCGGCGGCGCCA GTGGACGCGTGAGGCGGAGGCGCGGGCGGAGG___GAGGCCGGAGCGGGCAGCGCGGCGGCGCCA CCCT C UBALD1 Ensembl:ENSG00000153443 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:4614559..4614879;chr16:4614651..4614875;chr16:4614036..4614920;chr16:4614065..4614900;chr16:4614079..4614900 26863196 MeRIP-seq:(Medium) rs750697694 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_234936,Human_RBP_ID_763743,Human_RBP_ID_3506906,Human_RBP_ID_4400506,Human_RBP_ID_5113857,Human_RBP_ID_5141827,Human_RBP_ID_5316562,Human_RBP_ID_8084775,Human_RBP_ID_8726138,Human_RBP_ID_9324925,Human_RBP_ID_9419643,Human_RBP_ID_17371635,Human_RBP_ID_18162067,Human_RBP_ID_18418656,Human_RBP_ID_18482156,Human_RBP_ID_22713015,Human_RBP_ID_22738185,Human_RBP_ID_23118575,Human_RBP_ID_26779177,Human_RBP_ID_27837781 Human_Splice_Rec_1672495 73398 RMVar_ID_73398 Human_SNP_ID_591998951 m1A Human chr16 - 4614832 4614832 4614832 ATGGTGGACGCGTGAGGCGGAGGCGCGGGCGGAGGAGGGAGGCCGGAGCGGGCAGCGCGGCGGCG ATGGTGGACGCGTGAGGCGGAGGCGCGGGCGGCGGAGGGAGGCCGGAGCGGGCAGCGCGGCGGCG T G UBALD1 Ensembl:ENSG00000153443 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:4614651..4614875 26863196 MeRIP-seq:(Medium) rs860889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234936,Human_RBP_ID_763743,Human_RBP_ID_3506906,Human_RBP_ID_4400506,Human_RBP_ID_5113857,Human_RBP_ID_5141827,Human_RBP_ID_5316562,Human_RBP_ID_8084775,Human_RBP_ID_8726138,Human_RBP_ID_9324925,Human_RBP_ID_9419643,Human_RBP_ID_17371635,Human_RBP_ID_18162067,Human_RBP_ID_18418656,Human_RBP_ID_18482156,Human_RBP_ID_22713015,Human_RBP_ID_22738185,Human_RBP_ID_23118575,Human_RBP_ID_26779177,Human_RBP_ID_27837781 Human_Splice_Rec_1672495 73399 RMVar_ID_73399 Human_SNP_ID_592010255 m1A Human chr16 - 4645781 4645781 4645781 GCTGGCGTCCCAGCCACACTGGGGCAGGTCCCAGTAGCCTCCGAGGCCCCAGACAAGGCCACTCT GCTGGCGTCCCAGCCACACTGGGGCAGGTCCCCGTAGCCTCCGAGGCCCCAGACAAGGCCACTCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4645779..4645913 26863196 MeRIP-seq:(Medium) rs918673281 Functional Loss SNV dbSNP153 33..33 33 - - - 73400 RMVar_ID_73400 Human_SNP_ID_592019761 m1A Human chr16 + 4668533 4668530 4668534 TCACACATATATAGACACATAAACACACAGACACACACATACACACATAAACACACTCCTACTCG TCACACATATATAGACACATAAACACACAG____ACACATACACACATAAACACACTCCTACTCG GACAC G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4668528..4668675 26863196 MeRIP-seq:(Medium) rs767001731 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_198288,Human_RBP_ID_261419,Human_RBP_ID_2475327,Human_RBP_ID_26757175 RMVar_hsa_circ_117702,RMVar_hsa_circ_346567,RMVar_hsa_circ_176031,RMVar_hsa_circ_95755,RMVar_hsa_circ_365651,RMVar_hsa_circ_176032,RMVar_hsa_circ_176033,RMVar_hsa_circ_332204,RMVar_hsa_circ_176037,RMVar_hsa_circ_310455,RMVar_hsa_circ_332506,RMVar_hsa_circ_65226,RMVar_hsa_circ_325978,RMVar_hsa_circ_176039,RMVar_hsa_circ_311906,RMVar_hsa_circ_355241 73401 RMVar_ID_73401 Human_SNP_ID_592019762 m1A Human chr16 + 4668533 4668530 4668534 TCACACATATATAGACACATAAACACACAGACACACACATACACACATAAACACACTCCTACTCG TCACACATATATAGACACATAAACACACAGAC__ACACATACACACATAAACACACTCCTACTCG GACAC GAC MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4668528..4668675 26863196 MeRIP-seq:(Medium) rs767001731 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_198288,Human_RBP_ID_261419,Human_RBP_ID_2475327,Human_RBP_ID_26757175 RMVar_hsa_circ_117702,RMVar_hsa_circ_346567,RMVar_hsa_circ_176031,RMVar_hsa_circ_95755,RMVar_hsa_circ_365651,RMVar_hsa_circ_176032,RMVar_hsa_circ_176033,RMVar_hsa_circ_332204,RMVar_hsa_circ_176037,RMVar_hsa_circ_310455,RMVar_hsa_circ_332506,RMVar_hsa_circ_65226,RMVar_hsa_circ_325978,RMVar_hsa_circ_176039,RMVar_hsa_circ_311906,RMVar_hsa_circ_355241 73402 RMVar_ID_73402 Human_SNP_ID_592019766 m1A Human chr16 + 4668533 4668533 4668533 TCACACATATATAGACACATAAACACACAGACACACACATACACACATAAACACACTCCTACTCG TCACACATATATAGACACATAAACACACAGACGCACACATACACACATAAACACACTCCTACTCG A G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4668528..4668675 26863196 MeRIP-seq:(Medium) rs1223238187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_198288,Human_RBP_ID_261419,Human_RBP_ID_2475327,Human_RBP_ID_26757175 RMVar_hsa_circ_117702,RMVar_hsa_circ_346567,RMVar_hsa_circ_176031,RMVar_hsa_circ_95755,RMVar_hsa_circ_365651,RMVar_hsa_circ_176032,RMVar_hsa_circ_176033,RMVar_hsa_circ_332204,RMVar_hsa_circ_176037,RMVar_hsa_circ_310455,RMVar_hsa_circ_332506,RMVar_hsa_circ_65226,RMVar_hsa_circ_325978,RMVar_hsa_circ_176039,RMVar_hsa_circ_311906,RMVar_hsa_circ_355241 73403 RMVar_ID_73403 Human_SNP_ID_592021978 m1A Human chr16 + 4673480 4673480 4673480 GTACTCTGGCCTTTGGGAGGCTGCTGACCCACAAGCCCTTGTCCCGGCAGCCCTCGGACGACGAG GTACTCTGGCCTTTGGGAGGCTGCTGACCCACCAGCCCTTGTCCCGGCAGCCCTCGGACGACGAG A C MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4673476..4673575 26863196 MeRIP-seq:(Medium) rs778854640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890370,Human_RBP_ID_5357561,Human_RBP_ID_12742301,Human_RBP_ID_22415344,Human_RBP_ID_22651647,Human_RBP_ID_26780165 RMVar_hsa_circ_346567,RMVar_hsa_circ_95755,RMVar_hsa_circ_365651,RMVar_hsa_circ_176032,RMVar_hsa_circ_176033,RMVar_hsa_circ_332204,RMVar_hsa_circ_176037,RMVar_hsa_circ_310455,RMVar_hsa_circ_332506,RMVar_hsa_circ_325978,RMVar_hsa_circ_176039,RMVar_hsa_circ_176040,RMVar_hsa_circ_280600,RMVar_hsa_circ_311906,RMVar_hsa_circ_355241,RMVar_hsa_circ_285072,RMVar_hsa_circ_176041 73404 RMVar_ID_73404 Human_SNP_ID_592024076 m1A Human chr16 - 4678410 4678410 4678410 ATCTCTCTCATCCTGTCTCTGTGTCTCTCCACATTTGTCTCTGCCTCTCCCTGTGTCTCTCCACC ATCTCTCTCATCCTGTCTCTGTGTCTCTCCACCTTTGTCTCTGCCTCTCCCTGTGTCTCTCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4678389..4678562 26863196 MeRIP-seq:(Medium) rs542295218 Functional Loss SNV dbSNP153 33..33 33 - - - 73405 RMVar_ID_73405 Human_SNP_ID_592024111 m1A Human chr16 + 4678539 4678518 4678540 ATAGGAAGAGACAGACAGATGTGGAGAGACGGAGAGACAGATGTGGAGAGACAGGGTGAGAGAGA ATAGGAAGAGAC______________________AGACAGATGTGGAGAGACAGGGTGAGAGAGA CAGACAGATGTGGAGAGACGGAG C MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:4678318..4678680;chr16:4678309..4678672 26863196 MeRIP-seq:(Medium) rs934341893 Functional Loss DEL dbSNP153 13..34 33 - - - Human_RBP_ID_12742454 RMVar_hsa_circ_95755,RMVar_hsa_circ_176032,RMVar_hsa_circ_332506,RMVar_hsa_circ_355241,RMVar_hsa_circ_176042,RMVar_hsa_circ_311202,RMVar_hsa_circ_317732 73406 RMVar_ID_73406 Human_SNP_ID_592024805 m1A Human chr16 - 4680129 4680129 4680129 CTTGTCGTGGGTTTAAAAATGAGGGCGGGGGCAAAAAAACGTAGCCGGAGGACCAGACACTTACT CTTGTCGTGGGTTTAAAAATGAGGGCGGGGGCTAAAAAACGTAGCCGGAGGACCAGACACTTACT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:4680121..4680364;chr16:4680123..4680325 26863196 MeRIP-seq:(Medium) rs539216901 Functional Loss SNV dbSNP153 33..33 33 - - - 73407 RMVar_ID_73407 Human_SNP_ID_592024806 m1A Human chr16 - 4680129 4680129 4680129 CTTGTCGTGGGTTTAAAAATGAGGGCGGGGGCAAAAAAACGTAGCCGGAGGACCAGACACTTACT CTTGTCGTGGGTTTAAAAATGAGGGCGGGGGCGAAAAAACGTAGCCGGAGGACCAGACACTTACT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:4680121..4680364;chr16:4680123..4680325 26863196 MeRIP-seq:(Medium) rs539216901 Functional Loss SNV dbSNP153 33..33 33 - - - 73408 RMVar_ID_73408 Human_SNP_ID_592026076 m1A Human chr16 + 4682852 4682852 4682852 CAGCACCCTACGGTCCCCGTCTTCCCCCATCCACGAAGAGGATGAGGAGAAGCTCTCCGAGGACG CAGCACCCTACGGTCCCCGTCTTCCCCCATCCGCGAAGAGGATGAGGAGAAGCTCTCCGAGGACG A G MGRN1 Ensembl:ENSG00000102858 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4681667..4682863 32194978 MeRIP-seq:(Medium) rs1307747233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5359532,Human_RBP_ID_19070784 Human_Splice_Rec_1672544,Human_Splice_Rec_1672545,Human_Splice_Rec_1672576,Human_Splice_Rec_1672577,Human_Splice_Rec_1672604,Human_Splice_Rec_1672605,Human_Splice_Rec_1672638,Human_Splice_Rec_1672639,Human_Splice_Rec_1672670,Human_Splice_Rec_1672671,Human_Splice_Rec_1672700,Human_Splice_Rec_1672701,Human_Splice_Rec_1672730,Human_Splice_Rec_1672731,Human_Splice_Rec_1672806,Human_Splice_Rec_1672807,Human_Splice_Rec_1672814,Human_Splice_Rec_1672816,Human_Splice_Rec_1672817 RMVar_hsa_circ_95755,RMVar_hsa_circ_176032,RMVar_hsa_circ_332506,RMVar_hsa_circ_176043,RMVar_hsa_circ_355241,RMVar_hsa_circ_311202,RMVar_hsa_circ_290974 73409 RMVar_ID_73409 Human_SNP_ID_592026604 m1A Human chr16 - 4683927 4683927 4683927 CTCACCCCCAGACCCCCAGCCCCTTACCTGGCAGGTAGATGTCAGCAGGTGGGCCTCGGCCACAG CTCACCCCCAGACCCCCAGCCCCTTACCTGGCGGGTAGATGTCAGCAGGTGGGCCTCGGCCACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4683876..4683969 26863196 MeRIP-seq:(Medium) rs777091179 Functional Loss SNV dbSNP153 33..33 33 - - - 73410 RMVar_ID_73410 Human_SNP_ID_592028841 m1A Human chr16 - 4688878 4688866 4688878 TCTCAGAGTGGGGTCAGCTCGGCGGCGCTGGGATCGGGGCTGGGGCCACCAAGTGGAGGCCAGGT TCTCAGAGTGGGGTCAGCTCGGCGGCGCTGGG____________GCCACCAAGTGGAGGCCAGGT CCCCAGCCCCGAT C lnc-ANKS3-2 RNACentral:URS00008B3153 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4688795..4688948 26863196 MeRIP-seq:(Medium) rs1567250968 Functional Loss DEL dbSNP153 33..44 33 - - - 73411 RMVar_ID_73411 Human_SNP_ID_592028844 m1A Human chr16 + 4688870 4688870 4688870 CCAGCCCCACCTGGCCTCCACTTGGTGGCCCCAGCCCCGATCCCAGCGCCGCCGAGCTGACCCCA CCAGCCCCACCTGGCCTCCACTTGGTGGCCCCTGCCCCGATCCCAGCGCCGCCGAGCTGACCCCA A T MGRN1 Ensembl:ENSG00000102858 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4688776..4688978 26863196 MeRIP-seq:(Medium) rs1216373428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1672582,Human_Splice_Rec_1672610,Human_Splice_Rec_1672644,Human_Splice_Rec_1672706,Human_Splice_Rec_1672738 Human_miRNA_ID_1357187,Human_miRNA_ID_2685379 RMVar_hsa_circ_95755,RMVar_hsa_circ_176032 73412 RMVar_ID_73412 Human_SNP_ID_592029257 m1A Human chr16 + 4689674 4689674 4689674 CTTTGGTGACATCACAAGGCCCCTCCAGGTGCAGGGGCTTCTGTTTGGCAGGCCCCTGCCAGGGA CTTTGGTGACATCACAAGGCCCCTCCAGGTGCGGGGGCTTCTGTTTGGCAGGCCCCTGCCAGGGA A G MGRN1 Ensembl:ENSG00000102858 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4688929..4689728 32194978 MeRIP-seq:(Medium) rs538261853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474710,Human_RBP_ID_12742897 Human_miRNA_ID_2750981 RMVar_hsa_circ_95755,RMVar_hsa_circ_176032 73413 RMVar_ID_73413 Human_SNP_ID_592029449 m1A Human chr16 - 4690076 4690076 4690076 AGAAGCCTGAGACAGAACAAACCAAATCAGAGAGAACTGCAAGGGGGCCGGGCGCGGAGGCTCAC AGAAGCCTGAGACAGAACAAACCAAATCAGAGGGAACTGCAAGGGGGCCGGGCGCGGAGGCTCAC T C lnc-ANKS3-2 RNACentral:URS00008B3153 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4690026..4690326 32194978 MeRIP-seq:(Medium) rs1285963009 Functional Loss SNV dbSNP153 33..33 33 - - - 73414 RMVar_ID_73414 Human_SNP_ID_592029641 m1A Human chr16 - 4690482 4690482 4690482 GGCTGGCCTGGGTGTGCAGGGAGCTGGGTGTGAGGACCATGCTGTCCACTGCTGGGTCTCGCCCA GGCTGGCCTGGGTGTGCAGGGAGCTGGGTGTGGGGACCATGCTGTCCACTGCTGGGTCTCGCCCA T C lnc-ANKS3-2 RNACentral:URS00008B3153 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4690432..4690723 26863196 MeRIP-seq:(Medium) rs796442268 Functional Loss SNV dbSNP153 33..33 33 - - - 73415 RMVar_ID_73415 Human_SNP_ID_592029788 m1A Human chr16 + 4690725 4690725 4690725 CGGACCGAGCATCTCCCACGCACCTCTACCCCACCCCAAGCACCTCTCTCCCCCCATGCACCTCT CGGACCGAGCATCTCCCACGCACCTCTACCCCGCCCCAAGCACCTCTCTCCCCCCATGCACCTCT A G MGRN1 Ensembl:ENSG00000102858 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4690674..4690824 32194978 MeRIP-seq:(Medium) rs941986134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233298,Human_RBP_ID_474726,Human_RBP_ID_12742937,Human_RBP_ID_17077348,Human_RBP_ID_17371638,Human_RBP_ID_18938737,Human_RBP_ID_24531184 Human_miRNA_ID_1418571,Human_miRNA_ID_1702571,Human_miRNA_ID_2137197,Human_miRNA_ID_2665985 RMVar_hsa_circ_95755,RMVar_hsa_circ_176032 73416 RMVar_ID_73416 Human_SNP_ID_592031131 m1A Human chr16 - 4693796 4693796 4693796 GGCGTACAGCATGGCGTGGCACGAGTGGCTCCAGCCCGGCCCTAGGCGCATCGCCTCCACCCGGC GGCGTACAGCATGGCGTGGCACGAGTGGCTCCCGCCCGGCCCTAGGCGCATCGCCTCCACCCGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4693746..4693832 26863196 MeRIP-seq:(Medium) rs759590855 Functional Loss SNV dbSNP153 33..33 33 - - - 73417 RMVar_ID_73417 Human_SNP_ID_592032748 m1A Human chr16 - 4696610 4696610 4696610 ACCAGGCAGGGCCCTGGGGGGAAAGTGTATCCATATACACGCACAGGTGCCAACTGAGGTGGGAC ACCAGGCAGGGCCCTGGGGGGAAAGTGTATCCGTATACACGCACAGGTGCCAACTGAGGTGGGAC T C ANKS3 Ensembl:ENSG00000168096 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4696559..4698145 32194978 MeRIP-seq:(Medium) rs572033453 Functional Loss SNV dbSNP153 33..33 33 - - - 73418 RMVar_ID_73418 Human_SNP_ID_592033970 m1A Human chr16 + 4698779 4698779 4698779 GAGCCAACTCACGGGTGTCACCCTGCCCCCCCATCCCCCACCCAGCCACTCACCTTGTGCAGCTG GAGCCAACTCACGGGTGTCACCCTGCCCCCCCTTCCCCCACCCAGCCACTCACCTTGTGCAGCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4698776..4698886 26863196 MeRIP-seq:(Medium) rs951495757 Functional Loss SNV dbSNP153 33..33 33 - - - 73419 RMVar_ID_73419 Human_SNP_ID_592033995 m1A Human chr16 + 4698807 4698807 4698807 CCCCATCCCCCACCCAGCCACTCACCTTGTGCAGCTGGATGGCGAGCTCCTGCATCTCAGCCTCC CCCCATCCCCCACCCAGCCACTCACCTTGTGCGGCTGGATGGCGAGCTCCTGCATCTCAGCCTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4698393..4698943 32194978 MeRIP-seq:(Medium) rs1279293085 Functional Loss SNV dbSNP153 33..33 33 - - - 73420 RMVar_ID_73420 Human_SNP_ID_592034189 m1A Human chr16 + 4699127 4699127 4699127 AGATGCGGAGGTCCACGTCCTGCTCCTCAAACACCTGCAGGTACTTCAGACACCCGATCTGCTCC AGATGCGGAGGTCCACGTCCTGCTCCTCAAACCCCTGCAGGTACTTCAGACACCCGATCTGCTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4699089..4699189 26863196 MeRIP-seq:(Medium) rs1287062412 Functional Loss SNV dbSNP153 33..33 33 - - - 73421 RMVar_ID_73421 Human_SNP_ID_592035578 m1A Human chr16 + 4702153 4702153 4702153 GCTGCTCTCCACATCCCGCTCATTGATGGGGGAGGTGACATCCCGGCAGCAGAGGCCCTCTTCTT GCTGCTCTCCACATCCCGCTCATTGATGGGGGCGGTGACATCCCGGCAGCAGAGGCCCTCTTCTT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4702079..4705181 32194978 MeRIP-seq:(Medium) rs1448084231 Functional Loss SNV dbSNP153 33..33 33 - - - 73422 RMVar_ID_73422 Human_SNP_ID_592035579 m1A Human chr16 + 4702153 4702153 4702153 GCTGCTCTCCACATCCCGCTCATTGATGGGGGAGGTGACATCCCGGCAGCAGAGGCCCTCTTCTT GCTGCTCTCCACATCCCGCTCATTGATGGGGGGGGTGACATCCCGGCAGCAGAGGCCCTCTTCTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4702079..4705181 32194978 MeRIP-seq:(Medium) rs1448084231 Functional Loss SNV dbSNP153 33..33 33 - - - 73423 RMVar_ID_73423 Human_SNP_ID_592044629 m1A Human chr16 - 4726772 4726772 4726772 CGCACGTTCTGTGTTCTCTTGAAGCAAGGTGCAGAGCTAGAAATGAAAGACATCCAGGGCTGGAC CGCACGTTCTGTGTTCTCTTGAAGCAAGGTGCGGAGCTAGAAATGAAAGACATCCAGGGCTGGAC T C ANKS3 Ensembl:ENSG00000168096 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4726751..4727207 26863196 MeRIP-seq:(Medium) rs562824703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9372193 Human_Splice_Rec_1672844,Human_Splice_Rec_1672906,Human_Splice_Rec_1672956,Human_Splice_Rec_1672982,Human_Splice_Rec_1673010,Human_Splice_Rec_1673072,Human_Splice_Rec_1673102,Human_Splice_Rec_1673214,Human_Splice_Rec_1673226,Human_Splice_Rec_1673264,Human_Splice_Rec_1673274,Human_Splice_Rec_1673282,Human_Splice_Rec_1673290 Human_miRNA_ID_2395838,Human_miRNA_ID_2750982 RMVar_hsa_circ_268251,RMVar_hsa_circ_37489,RMVar_hsa_circ_18417,RMVar_hsa_circ_1600,RMVar_hsa_circ_176049,RMVar_hsa_circ_329675,RMVar_hsa_circ_37118,RMVar_hsa_circ_318747,RMVar_hsa_circ_276561,RMVar_hsa_circ_176052,RMVar_hsa_circ_36914,RMVar_hsa_circ_176053 73424 RMVar_ID_73424 Human_SNP_ID_592045870 m1A Human chr16 - 4730149 4730149 4730149 AAGATCTAACCCTTGGGCCTTCCTCCTCAGTGATGTCCGAGCTCAGCGATGAAGCCAGCGAGCCG AAGATCTAACCCTTGGGCCTTCCTCCTCAGTGCTGTCCGAGCTCAGCGATGAAGCCAGCGAGCCG T G ANKS3,AC020663.1 Ensembl:ENSG00000168096,Ensembl:ENSG00000266994 Protein coding,lincRNA start codon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4730101..4730186 26863196 MeRIP-seq:(Medium) rs1378918646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4395604 Human_Splice_Rec_1672872,Human_Splice_Rec_1672902,Human_Splice_Rec_1673038,Human_Splice_Rec_1673070,Human_Splice_Rec_1673148,Human_Splice_Rec_1673172,Human_Splice_Rec_1673186,Human_Splice_Rec_1673210,Human_Splice_Rec_1673224,Human_Splice_Rec_1673240,Human_Splice_Rec_1673248,Human_Splice_Rec_1673254,Human_Splice_Rec_1673262,Human_Splice_Rec_1673270,Human_Splice_Rec_1673278,Human_Splice_Rec_1673286,Human_Splice_Rec_1673292,Human_Splice_Rec_1673300 RMVar_hsa_circ_268251,RMVar_hsa_circ_329675,RMVar_hsa_circ_318747,RMVar_hsa_circ_176053,RMVar_hsa_circ_329554 73425 RMVar_ID_73425 Human_SNP_ID_592047331 m1A Human chr16 + 4734212 4734211 4734212 CCGCCCTCGGGCTGCCGTCGCCAACCCCCCCCAAACAGCTCGCCGCCACGCTCCCTCGCCGGGGC CCGCCCTCGGGCTGCCGTCGCCAACCCCCCCC_AACAGCTCGCCGCCACGCTCCCTCGCCGGGGC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4729957..4735011 26863196 MeRIP-seq:(Medium) rs1432820856 Functional Loss DEL dbSNP153 33..33 33 - - - 73426 RMVar_ID_73426 Human_SNP_ID_592047334 m1A Human chr16 + 4734216 4734216 4734216 CCTCGGGCTGCCGTCGCCAACCCCCCCCAAACAGCTCGCCGCCACGCTCCCTCGCCGGGGCACCG CCTCGGGCTGCCGTCGCCAACCCCCCCCAAACCGCTCGCCGCCACGCTCCCTCGCCGGGGCACCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4734130..4734230 26863196 MeRIP-seq:(Medium) rs1343332505 Functional Loss SNV dbSNP153 33..33 33 - - - 73427 RMVar_ID_73427 Human_SNP_ID_592057733 m1A Human chr16 - 4762889 4762889 4762889 GCTGCAGGGAACACTGCCACACGGCTGGGCAGAGGGAGGGAGGCTGCAGACAGCCCGGGGGTGGG GCTGCAGGGAACACTGCCACACGGCTGGGCAGGGGGAGGGAGGCTGCAGACAGCCCGGGGGTGGG T C ZNF500 Ensembl:ENSG00000103199 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4762865..4763000 26863196 MeRIP-seq:(Medium) rs976192044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19000,RMVar_hsa_circ_176054,RMVar_hsa_circ_333652 73428 RMVar_ID_73428 Human_SNP_ID_592058822 m1A Human chr16 + 4765625 4765625 4765625 TGCAGCCCTTCCACAAGGACCACGGCCTCCTCACCGCTCTCCGGCTGCTGCTCGCGTACCCGAGC TGCAGCCCTTCCACAAGGACCACGGCCTCCTCTCCGCTCTCCGGCTGCTGCTCGCGTACCCGAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:4765578..4765687;chr16:4765584..4765696 26863196 MeRIP-seq:(Medium) rs1429336420 Functional Loss SNV dbSNP153 33..33 33 - - - 73429 RMVar_ID_73429 Human_SNP_ID_592072040 m1A Human chr16 - 4798145 4798145 4798145 TCGCCCCTGCCCTGCCGTCCGACCTGCTGGTCAACGTCTACATCAACCTCAACAAGCTCTGCCTC TCGCCCCTGCCCTGCCGTCCGACCTGCTGGTCGACGTCTACATCAACCTCAACAAGCTCTGCCTC T C AC020663.5,ROGDI Ensembl:ENSG00000285952,Ensembl:ENSG00000067836 lincRNA,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4798094..4798682 26863196 MeRIP-seq:(Medium) rs747029547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891410,Human_RBP_ID_9373741 Human_Splice_Rec_1673482,Human_Splice_Rec_1673483,Human_Splice_Rec_1673570,Human_Splice_Rec_1673571,Human_Splice_Rec_1673582,Human_Splice_Rec_1673583,Human_Splice_Rec_1673600,Human_Splice_Rec_1673601,Human_Splice_Rec_1673620,Human_Splice_Rec_1673621,Human_Splice_Rec_1673638,Human_Splice_Rec_1673639,Human_Splice_Rec_1673658,Human_Splice_Rec_1673659,Human_Splice_Rec_1673674,Human_Splice_Rec_1673675,Human_Splice_Rec_1673684,Human_Splice_Rec_1673685,Human_Splice_Rec_1673692,Human_Splice_Rec_1673693,Human_Splice_Rec_1673706,Human_Splice_Rec_1673707,Human_Splice_Rec_1673720,Human_Splice_Rec_1673721 RMVar_hsa_circ_83322,RMVar_hsa_circ_344900,RMVar_hsa_circ_176056,RMVar_hsa_circ_80288,RMVar_hsa_circ_176057,RMVar_hsa_circ_176055 73430 RMVar_ID_73430 Human_SNP_ID_592072043 m1A Human chr16 + 4798147 4798147 4798147 GGCAGAGCTTGTTGAGGTTGATGTAGACGTTGACCAGCAGGTCGGACGGCAGGGCAGGGGCGAAC GGCAGAGCTTGTTGAGGTTGATGTAGACGTTGGCCAGCAGGTCGGACGGCAGGGCAGGGGCGAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4798014..4798213 26863196 MeRIP-seq:(Medium) rs1567598260 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_328 73431 RMVar_ID_73431 Human_SNP_ID_592072282 m1A Human chr16 + 4798621 4798621 4798621 TCTCGGGGAGGGTGAGGGTGGCGGGGGTGGTGAGCCGGTTTCGGGCTCTGGTCAGCTGCAGCATC TCTCGGGGAGGGTGAGGGTGGCGGGGGTGGTGGGCCGGTTTCGGGCTCTGGTCAGCTGCAGCATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4798558..4798657 26863196 MeRIP-seq:(Medium) rs1436982723 Functional Loss SNV dbSNP153 33..33 33 - - - 73432 RMVar_ID_73432 Human_SNP_ID_592072307 m1A Human chr16 - 4798664 4798664 4798664 CGCAGAGCCAACCCCGCCTCTCCCTGCAGCTGATGGACGCAGTGATGCTGCAGCTGACCAGAGCC CGCAGAGCCAACCCCGCCTCTCCCTGCAGCTGTTGGACGCAGTGATGCTGCAGCTGACCAGAGCC T A AC020663.5,ROGDI Ensembl:ENSG00000285952,Ensembl:ENSG00000067836 lincRNA,Protein coding exon,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4798513..4798713 32194978 MeRIP-seq:(Medium) rs886052037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18983142 Human_Splice_Rec_1673480,Human_Splice_Rec_1673481,Human_Splice_Rec_1673568,Human_Splice_Rec_1673569,Human_Splice_Rec_1673580,Human_Splice_Rec_1673581,Human_Splice_Rec_1673598,Human_Splice_Rec_1673599,Human_Splice_Rec_1673618,Human_Splice_Rec_1673619,Human_Splice_Rec_1673637,Human_Splice_Rec_1673656,Human_Splice_Rec_1673657,Human_Splice_Rec_1673672,Human_Splice_Rec_1673673,Human_Splice_Rec_1673682,Human_Splice_Rec_1673683,Human_Splice_Rec_1673704,Human_Splice_Rec_1673705,Human_Splice_Rec_1673718,Human_Splice_Rec_1673719,Human_Splice_Rec_1673734 Human_miRNA_ID_1938038,Human_miRNA_ID_1949138 Clinvar_Rec_329 RMVar_hsa_circ_83322,RMVar_hsa_circ_176056,RMVar_hsa_circ_80288,RMVar_hsa_circ_176055 73433 RMVar_ID_73433 Human_SNP_ID_592072308 m1A Human chr16 - 4798664 4798664 4798664 CGCAGAGCCAACCCCGCCTCTCCCTGCAGCTGATGGACGCAGTGATGCTGCAGCTGACCAGAGCC CGCAGAGCCAACCCCGCCTCTCCCTGCAGCTGGTGGACGCAGTGATGCTGCAGCTGACCAGAGCC T C AC020663.5,ROGDI Ensembl:ENSG00000285952,Ensembl:ENSG00000067836 lincRNA,Protein coding exon,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4798513..4798713 32194978 MeRIP-seq:(Medium) rs886052037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18983142 Human_Splice_Rec_1673480,Human_Splice_Rec_1673481,Human_Splice_Rec_1673568,Human_Splice_Rec_1673569,Human_Splice_Rec_1673580,Human_Splice_Rec_1673581,Human_Splice_Rec_1673598,Human_Splice_Rec_1673599,Human_Splice_Rec_1673618,Human_Splice_Rec_1673619,Human_Splice_Rec_1673637,Human_Splice_Rec_1673656,Human_Splice_Rec_1673657,Human_Splice_Rec_1673672,Human_Splice_Rec_1673673,Human_Splice_Rec_1673682,Human_Splice_Rec_1673683,Human_Splice_Rec_1673704,Human_Splice_Rec_1673705,Human_Splice_Rec_1673718,Human_Splice_Rec_1673719,Human_Splice_Rec_1673734 Human_miRNA_ID_1938038,Human_miRNA_ID_1949138 Clinvar_Rec_329 RMVar_hsa_circ_83322,RMVar_hsa_circ_176056,RMVar_hsa_circ_80288,RMVar_hsa_circ_176055 73434 RMVar_ID_73434 Human_SNP_ID_592073147 m1A Human chr16 - 4800577 4800577 4800577 CTGCCCAGCTCACCCCACTCTTGCCTGTCAGGATGTGAACCTGAAGATGCCCCGGAACAACCAGC CTGCCCAGCTCACCCCACTCTTGCCTGTCAGGTTGTGAACCTGAAGATGCCCCGGAACAACCAGC T A AC020663.5,ROGDI Ensembl:ENSG00000285952,Ensembl:ENSG00000067836 lincRNA,Protein coding exon,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4800511..4800611 32194978 MeRIP-seq:(Medium) rs774073956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22542195,Human_RBP_ID_22652909 Human_Splice_Rec_1673477,Human_Splice_Rec_1673564,Human_Splice_Rec_1673565,Human_Splice_Rec_1673577,Human_Splice_Rec_1673594,Human_Splice_Rec_1673595,Human_Splice_Rec_1673614,Human_Splice_Rec_1673615,Human_Splice_Rec_1673633,Human_Splice_Rec_1673645,Human_Splice_Rec_1673652,Human_Splice_Rec_1673653,Human_Splice_Rec_1673668,Human_Splice_Rec_1673669,Human_Splice_Rec_1673689,Human_Splice_Rec_1673700,Human_Splice_Rec_1673701,Human_Splice_Rec_1673714,Human_Splice_Rec_1673715,Human_Splice_Rec_1673730,Human_Splice_Rec_1673731 RMVar_hsa_circ_83322,RMVar_hsa_circ_176055 73435 RMVar_ID_73435 Human_SNP_ID_592073448 m1A Human chr16 - 4801223 4801223 4801223 GGCCCTGTCCCCTCCCATCCTGCCAATGGGGAAGAGCATGGGAGCTCCCACTTTCTCTCTGTACA GGCCCTGTCCCCTCCCATCCTGCCAATGGGGAGGAGCATGGGAGCTCCCACTTTCTCTCTGTACA T C AC020663.5,ROGDI Ensembl:ENSG00000285952,Ensembl:ENSG00000067836 lincRNA,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4801221..4801356 26863196 MeRIP-seq:(Medium) rs1378646791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5357576 Human_Splice_Rec_1673562,Human_Splice_Rec_1673612,Human_Splice_Rec_1673632,Human_Splice_Rec_1673666,Human_Splice_Rec_1673712,Human_Splice_Rec_1673728 73436 RMVar_ID_73436 Human_SNP_ID_592079235 m1A Human chr16 - 4814587 4814587 4814587 GTCTGGGAAGAACCCCCGCTGAAGTCGTCTCAACCTGCGACATCACTTTCGCCTGCGTGTCGGAT GTCTGGGAAGAACCCCCGCTGAAGTCGTCTCAGCCTGCGACATCACTTTCGCCTGCGTGTCGGAT T C GLYR1 Ensembl:ENSG00000140632 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs761912115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1673758,Human_Splice_Rec_1673759,Human_Splice_Rec_1673790,Human_Splice_Rec_1673791,Human_Splice_Rec_1673820,Human_Splice_Rec_1673821,Human_Splice_Rec_1673850,Human_Splice_Rec_1673851,Human_Splice_Rec_1673861,Human_Splice_Rec_1673886,Human_Splice_Rec_1673887,Human_Splice_Rec_1673898 RMVar_hsa_circ_16382,RMVar_hsa_circ_121849,RMVar_hsa_circ_311193,RMVar_hsa_circ_347072,RMVar_hsa_circ_97785,RMVar_hsa_circ_38021,RMVar_hsa_circ_176062,RMVar_hsa_circ_176064,RMVar_hsa_circ_176065,RMVar_hsa_circ_176063,RMVar_hsa_circ_176061,RMVar_hsa_circ_34231,RMVar_hsa_circ_111148,RMVar_hsa_circ_267903,RMVar_hsa_circ_176066,RMVar_hsa_circ_352529,RMVar_hsa_circ_265035 73437 RMVar_ID_73437 Human_SNP_ID_592088483 m1A Human chr16 - 4840116 4840116 4840116 GCGTTTAAGAGGTGGTGTAAACAGGTATTGCAAGGGGATTTTTTAGGGATGAGAACTAACTTGTG GCGTTTAAGAGGTGGTGTAAACAGGTATTGCAGGGGGATTTTTTAGGGATGAGAACTAACTTGTG T C AC020663.3,GLYR1 Ensembl:ENSG00000275056,Ensembl:ENSG00000140632 lincRNA,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4840114..4840327 26863196 MeRIP-seq:(Medium) rs909174057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12747263 RMVar_hsa_circ_121849,RMVar_hsa_circ_176065,RMVar_hsa_circ_311507,RMVar_hsa_circ_127807,RMVar_hsa_circ_364311,RMVar_hsa_circ_313648,RMVar_hsa_circ_176072,RMVar_hsa_circ_176073,RMVar_hsa_circ_317087,RMVar_hsa_circ_265905 73438 RMVar_ID_73438 Human_SNP_ID_592090692 m1A Human chr16 - 4846159 4846159 4846159 CCTCCTTGGCCAGGAAAGGTGAGTGTCTTGCTACTAAAGGAAGAGATCTGAAGTTGGGTTTGAAG CCTCCTTGGCCAGGAAAGGTGAGTGTCTTGCTGCTAAAGGAAGAGATCTGAAGTTGGGTTTGAAG T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4846151..4846250 26863410 MeRIP-seq:(Medium) rs373935041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891418,Human_RBP_ID_5356461,Human_RBP_ID_19073249,Human_RBP_ID_22651661,Human_RBP_ID_26779181 Human_Splice_Rec_1673770,Human_Splice_Rec_1673804,Human_Splice_Rec_1673832,Human_Splice_Rec_1673868,Human_Splice_Rec_1673900,Human_Splice_Rec_1673932 RMVar_hsa_circ_127807,RMVar_hsa_circ_176073,RMVar_hsa_circ_265905 73439 RMVar_ID_73439 Human_SNP_ID_592091155 m1A Human chr16 + 4847177 4847177 4847177 CAGCTCCAGGGCCGGCAGCGAACCCCGCGCCCAGGCGGGTAGCTCCCCGGCGCGTCTCGGTTGGC CAGCTCCAGGGCCGGCAGCGAACCCCGCGCCCGGGCGGGTAGCTCCCCGGCGCGTCTCGGTTGGC A G UBN1 Ensembl:ENSG00000118900 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4847175..4847260 26863196 MeRIP-seq:(Medium) rs1308216331 Functional Loss SNV dbSNP153 33..33 33 - - - 73440 RMVar_ID_73440 Human_SNP_ID_592091165 m1A Human chr16 - 4847188 4847188 4847188 CGAGCGGCCGGGCCAACCGAGACGCGCCGGGGAGCTACCCGCCTGGGCGCGGGGTTCGCTGCCGG CGAGCGGCCGGGCCAACCGAGACGCGCCGGGGGGCTACCCGCCTGGGCGCGGGGTTCGCTGCCGG T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4847185..4847255 26863196 MeRIP-seq:(Medium) rs1341116798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889425,Human_RBP_ID_26780174 73441 RMVar_ID_73441 Human_SNP_ID_592091445 m1A Human chr16 - 4847562 4847562 4847562 GCGAGCCGCGAGGCCGGCTCCCTCTCGCGCTCAGCCGGTCGCACCGTCGCCGCCGCCGCCGCCTC GCGAGCCGCGAGGCCGGCTCCCTCTCGCGCTCTGCCGGTCGCACCGTCGCCGCCGCCGCCGCCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4847513..4847707 26863196 MeRIP-seq:(Medium) rs1029836133 Functional Loss SNV dbSNP153 33..33 33 - - - 73442 RMVar_ID_73442 Human_SNP_ID_592091534 m1A Human chr16 + 4847719 4847719 4847719 CCCGAGGCGCTGGTCGGCCCCGTCGCAGCGCCAGTGAGCTACCCTGACGGAGCTCGGCGCGGCCT CCCGAGGCGCTGGTCGGCCCCGTCGCAGCGCCGGTGAGCTACCCTGACGGAGCTCGGCGCGGCCT A G UBN1 Ensembl:ENSG00000118900 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:4847587..4847719 26863196 MeRIP-seq:(Medium) rs1007033529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4371223,Human_RBP_ID_5419392,Human_RBP_ID_5440631,Human_RBP_ID_5495764,Human_RBP_ID_18680161,Human_RBP_ID_27443120 73443 RMVar_ID_73443 Human_SNP_ID_592098408 m1A Human chr16 + 4867195 4867195 4867195 GAAGGGAGTGGCGGTCTTAAGGTTGGAGTGCAATTATTAGAAGTGGGGAACACAGGGGAAGAGCA GAAGGGAGTGGCGGTCTTAAGGTTGGAGTGCAGTTATTAGAAGTGGGGAACACAGGGGAAGAGCA A G UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:4867064..4867214 26863196 MeRIP-seq:(Medium) rs112619455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8184,RMVar_hsa_circ_39825 73444 RMVar_ID_73444 Human_SNP_ID_592099762 m1A Human chr16 + 4870884 4870884 4870884 AAGAGGAGAAAGACAAGGAGCAGAGGGACCGGATTTGTTCGGATGAGGAAGAAGATGAAGAAAAA AAGAGGAGAAAGACAAGGAGCAGAGGGACCGGGTTTGTTCGGATGAGGAAGAAGATGAAGAAAAA A G UBN1 Ensembl:ENSG00000118900 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4870860..4871193 26863196 MeRIP-seq:(Medium) rs200486174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46136,Human_RBP_ID_4371308,Human_RBP_ID_6517118,Human_RBP_ID_9345727,Human_RBP_ID_9372214,Human_RBP_ID_18985412,Human_RBP_ID_26329759,Human_RBP_ID_27810849 Human_Splice_Rec_1673966,Human_Splice_Rec_1673967,Human_Splice_Rec_1674000,Human_Splice_Rec_1674001,Human_Splice_Rec_1674030,Human_Splice_Rec_1674031,Human_Splice_Rec_1674057 RMVar_hsa_circ_9360,RMVar_hsa_circ_8184,RMVar_hsa_circ_39825,RMVar_hsa_circ_354341 73445 RMVar_ID_73445 Human_SNP_ID_592105042 m1A Human chr16 + 4884606 4884606 4884606 CCTCCTCATACCTGACCACCTCCTGCTGCACCACCCTTTCCTTCACCCGCGAGAGCTCCTCCTCT CCTCCTCATACCTGACCACCTCCTGCTGCACCGCCCTTTCCTTCACCCGCGAGAGCTCCTCCTCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:4884513..4884667 26863196 MeRIP-seq:(Medium) rs764668681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20170480 73446 RMVar_ID_73446 Human_SNP_ID_592105550 m1A Human chr16 - 4885492 4885492 4885492 AGAAGAGCCGGGCGCAGGAGAAGGTCACAGAGAAAGAGGTGGTGAAACTGCAGAATGACCCCCAG AGAAGAGCCGGGCGCAGGAGAAGGTCACAGAGGAAGAGGTGGTGAAACTGCAGAATGACCCCCAG T C PPL Ensembl:ENSG00000118898 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4884053..4886000 26863196 MeRIP-seq:(Medium) rs1352815259 Functional Loss SNV dbSNP153 33..33 33 - - - 73447 RMVar_ID_73447 Human_SNP_ID_592123876 m1A Human chr16 + 4936722 4936722 4936722 CCCAGCTCAGCTGCCCGTGCCCTAGGCCCTCAAGGCAATGCTCCCTGGGCTCCCGGAGTCCCCTG CCCAGCTCAGCTGCCCGTGCCCTAGGCCCTCATGGCAATGCTCCCTGGGCTCCCGGAGTCCCCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4936718..4936859 26863196 MeRIP-seq:(Medium) rs72633280 Functional Loss SNV dbSNP153 33..33 33 - - - 73448 RMVar_ID_73448 Human_SNP_ID_592156142 m1A Human chr16 - 5025633 5025633 5025633 CCCTGGCGCTGGCCTTCCTCCTGCTGATCAGCACTGCAGCAAACCTGTCCTTGCTCCTGTCCAGA CCCTGGCGCTGGCCTTCCTCCTGCTGATCAGCGCTGCAGCAAACCTGTCCTTGCTCCTGTCCAGA T C NAGPA Ensembl:ENSG00000103174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:5025491..5027190 32194978 MeRIP-seq:(Medium) rs1449488745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22441267,Human_RBP_ID_22760082 Human_Splice_Rec_1674234,Human_Splice_Rec_1674252,Human_Splice_Rec_1674258,Human_Splice_Rec_1674278,Human_Splice_Rec_1674318 73449 RMVar_ID_73449 Human_SNP_ID_592172592 m1A Human chr16 - 5071881 5071881 5071881 CTCCCAGCAGCAGCAGCGGCAGCAGCAGACACAGCGCCAGCAGGACCAAGCATGAGGCCGCCATC CTCCCAGCAGCAGCAGCGGCAGCAGCAGACACGGCGCCAGCAGGACCAAGCATGAGGCCGCCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:5071826..5071993 26863196 MeRIP-seq:(Medium) rs760924780 Functional Loss SNV dbSNP153 33..33 33 - - - 73450 RMVar_ID_73450 Human_SNP_ID_593669105 m1A Human chr16 - 8621777 8621777 8621777 CTACCCTATCCCGCCGCCTCTCCCAGGCACTTACCCGCCGCGGGGCCCAGCCTGGGATCCCACCC CTACCCTATCCCGCCGCCTCTCCCAGGCACTTGCCCGCCGCGGGGCCCAGCCTGGGATCCCACCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:8621746..8621834;chr16:8621744..8621853;chr16:8621753..8621837 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1252179359 Functional Loss SNV dbSNP153 33..33 33 - - - 73451 RMVar_ID_73451 Human_SNP_ID_593674944 m1A Human chr16 - 8639490 8639490 8639490 AGCAGCAAGTGAAGTGGACTGGCTTGCATCTGAGAAAGGGCACTCTGGATGTTTCATGAGGACAT AGCAGCAAGTGAAGTGGACTGGCTTGCATCTGGGAAAGGGCACTCTGGATGTTTCATGAGGACAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8639454..8639688 26863196 MeRIP-seq:(Medium) rs1208604384 Functional Loss SNV dbSNP153 33..33 33 - - - 73452 RMVar_ID_73452 Human_SNP_ID_593674945 m1A Human chr16 - 8639490 8639490 8639490 AGCAGCAAGTGAAGTGGACTGGCTTGCATCTGAGAAAGGGCACTCTGGATGTTTCATGAGGACAT AGCAGCAAGTGAAGTGGACTGGCTTGCATCTGCGAAAGGGCACTCTGGATGTTTCATGAGGACAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8639454..8639688 26863196 MeRIP-seq:(Medium) rs1208604384 Functional Loss SNV dbSNP153 33..33 33 - - - 73453 RMVar_ID_73453 Human_SNP_ID_593677038 m1A Human chr16 + 8644634 8644634 8644634 CGATCACTTCCGCTCCTGCCTGCACGCGCTGGAGCAGCTCGCAGATGGCAAGCTGCGCTTCGTGG CGATCACTTCCGCTCCTGCCTGCACGCGCTGGGGCAGCTCGCAGATGGCAAGCTGCGCTTCGTGG A G METTL22 Ensembl:ENSG00000067365 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:8644584..8644684 32194978 MeRIP-seq:(Medium) rs201309316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481131,Human_RBP_ID_26328051 Human_Splice_Rec_1675276,Human_Splice_Rec_1675277,Human_Splice_Rec_1675296,Human_Splice_Rec_1675297,Human_Splice_Rec_1675322,Human_Splice_Rec_1675323,Human_Splice_Rec_1675348,Human_Splice_Rec_1675349,Human_Splice_Rec_1675363,Human_Splice_Rec_1675380,Human_Splice_Rec_1675381,Human_Splice_Rec_1675388,Human_Splice_Rec_1675389,Human_Splice_Rec_1675396,Human_Splice_Rec_1675400,Human_Splice_Rec_1675401 RMVar_hsa_circ_116245,RMVar_hsa_circ_176140,RMVar_hsa_circ_176142,RMVar_hsa_circ_121968,RMVar_hsa_circ_347127,RMVar_hsa_circ_373008,RMVar_hsa_circ_176146 73454 RMVar_ID_73454 Human_SNP_ID_593678155 m1A Human chr16 + 8647048 8647048 8647048 AGCCCCTTTCCCCTGCCTTGCTGCTGCCGCACACTTTGCACCAGGGCCTTTCATGGCCCCTTTCC AGCCCCTTTCCCCTGCCTTGCTGCTGCCGCACGCTTTGCACCAGGGCCTTTCATGGCCCCTTTCC A G METTL22 Ensembl:ENSG00000067365 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:8646999..8647131 26863196 MeRIP-seq:(Medium) rs1190660755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18939969 73455 RMVar_ID_73455 Human_SNP_ID_593723597 m1A Human chr16 + 8783005 8783005 8783005 CATCGACCTATTTTTGTTGAAGAATGAAAGGCAATGACAAGTTTAACATATACAAATTCGTGAAT CATCGACCTATTTTTGTTGAAGAATGAAAGGCGATGACAAGTTTAACATATACAAATTCGTGAAT A G ABAT Ensembl:ENSG00000183044 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs45615432 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_330,Clinvar_Rec_331,Clinvar_Rec_332,Clinvar_Rec_333,Clinvar_Rec_334 GWAS_ID_8902,GWAS_ID_8903,GWAS_ID_8904,GWAS_ID_8905,GWAS_ID_8906,GWAS_ID_8907,GWAS_ID_8908 73456 RMVar_ID_73456 Human_SNP_ID_593727798 m1A Human chr16 - 8796479 8796479 8796479 GTGGGCAGGAGGATCCTAAGAGGTGGGTGGGCAGCAGTTCACCCATCTCGAAGGAGAAACTACCA GTGGGCAGGAGGATCCTAAGAGGTGGGTGGGCGGCAGTTCACCCATCTCGAAGGAGAAACTACCA T C TMEM186 Ensembl:ENSG00000184857 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:8796428..8796578 32194978 MeRIP-seq:(Medium) rs148298211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393592,Human_RBP_ID_27447206 RMVar_hsa_circ_176159,RMVar_hsa_circ_116756 73457 RMVar_ID_73457 Human_SNP_ID_593728411 m1A Human chr16 + 8797934 8797934 8797934 CGCTCTGCCTCTTCGACGTGGATGGGACCCTCACCGCCCCGCGGCAGGTAAGTGGCGGCCGGCGG CGCTCTGCCTCTTCGACGTGGATGGGACCCTCCCCGCCCCGCGGCAGGTAAGTGGCGGCCGGCGG A C PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:8797890..8797975 26863196 MeRIP-seq:(Medium) rs757040733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393594,Human_RBP_ID_9373772,Human_RBP_ID_23113879,Human_RBP_ID_26329763 Human_Splice_Rec_1675665,Human_Splice_Rec_1675671,Human_Splice_Rec_1675683,Human_Splice_Rec_1675693,Human_Splice_Rec_1675697,Human_Splice_Rec_1675711,Human_Splice_Rec_1675715,Human_Splice_Rec_1675725,Human_Splice_Rec_1675735,Human_Splice_Rec_1675747,Human_Splice_Rec_1675757,Human_Splice_Rec_1675765,Human_Splice_Rec_1675775,Human_Splice_Rec_1675783 73458 RMVar_ID_73458 Human_SNP_ID_593729779 m1A Human chr16 - 8801863 8801863 8801863 GCTCCTGCACTTTCTCAAAGTCCGATCCGCCTACCACTCCGATTTTGATCTTCTGCCTCAATTTT GCTCCTGCACTTTCTCAAAGTCCGATCCGCCTGCCACTCCGATTTTGATCTTCTGCCTCAATTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8801761..8801866 26863196 MeRIP-seq:(Medium) rs104894534 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_335 GWAS_ID_8909 73459 RMVar_ID_73459 Human_SNP_ID_593740297 m1A Human chr16 + 8833971 8833971 8833971 GTGTAAACCGGCAGTGTAAACAAGAGCAGGGCATGTATGAGTAGTTGAGAATGGCGAATAGGAAT GTGTAAACCGGCAGTGTAAACAAGAGCAGGGCGTGTATGAGTAGTTGAGAATGGCGAATAGGAAT A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8833961..8834078 26863196 MeRIP-seq:(Medium) rs1350548599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12847447,Human_RBP_ID_23706433 73460 RMVar_ID_73460 Human_SNP_ID_593740939 m1A Human chr16 - 8835507 8835507 8835507 TACTACCCATTATTCTGTTCTGGATCTCAAACATGCTTTCTTTACTATTCCTTTGCACCCTTCAT TACTACCCATTATTCTGTTCTGGATCTCAAACGTGCTTTCTTTACTATTCCTTTGCACCCTTCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8835496..8835636 26863196 MeRIP-seq:(Medium) rs780317194 Functional Loss SNV dbSNP153 33..33 33 - - - 73461 RMVar_ID_73461 Human_SNP_ID_593740965 m1A Human chr16 - 8835575 8835575 8835575 CAAATTGTTTTGCCTATCCACCCCGTGGTGCCAAACCCATATACTCTCCTGTCCTCAATACCTCC CAAATTGTTTTGCCTATCCACCCCGTGGTGCCCAACCCATATACTCTCCTGTCCTCAATACCTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8835394..8835636 26863196 MeRIP-seq:(Medium) rs903389503 Functional Loss SNV dbSNP153 33..33 33 - - - 73462 RMVar_ID_73462 Human_SNP_ID_593741793 m1A Human chr16 - 8837415 8837415 8837415 TCTCCCTTAGCCTGTGTTCTTAAGAACTTAAAACCTCTTCAACTCACACCTGACCTAAAACCTAA TCTCCCTTAGCCTGTGTTCTTAAGAACTTAAACCCTCTTCAACTCACACCTGACCTAAAACCTAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8837402..8837572 26863196 MeRIP-seq:(Medium) rs1298427522 Functional Loss SNV dbSNP153 33..33 33 - - - 73463 RMVar_ID_73463 Human_SNP_ID_593742522 m1A Human chr16 - 8839309 8839309 8839309 TTTTACTTTACATCTCCAGTTTTGCCTCGCACAAGGTCTCTTCTTCCTCTGTGGATCCTTTACCT TTTTACTTTACATCTCCAGTTTTGCCTCGCACGAGGTCTCTTCTTCCTCTGTGGATCCTTTACCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8839299..8839384 26863196 MeRIP-seq:(Medium) rs1442930432 Functional Loss SNV dbSNP153 33..33 33 - - - 73464 RMVar_ID_73464 Human_SNP_ID_593743678 m1A Human chr16 + 8842353 8842353 8842353 TGTTGAGAAGATTCAAAGGAGGGGCTACAAAGAAGAAGGTCATCAATATATTAAATAAGGTGAGA TGTTGAGAAGATTCAAAGGAGGGGCTACAAAGTAGAAGGTCATCAATATATTAAATAAGGTGAGA A T PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8842340..8842431 26863196 MeRIP-seq:(Medium) rs190581861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1675801 73465 RMVar_ID_73465 Human_SNP_ID_593743762 m1A Human chr16 - 8842573 8842573 8842573 CTCCACAACTCACTATTCCACACTTGATCTTAAAGATGCTTCTTTCAGCGTTCCCCTGCACCCCT CTCCACAACTCACTATTCCACACTTGATCTTAGAGATGCTTCTTTCAGCGTTCCCCTGCACCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8842522..8842618 26863196 MeRIP-seq:(Medium) rs951502371 Functional Loss SNV dbSNP153 33..33 33 - - - 73466 RMVar_ID_73466 Human_SNP_ID_593748305 m1A Human chr16 - 8853026 8853026 8853026 GGAGGGACGGAGGGTTTTGGTGACAGAGCGAGAGCTAAAATTGAGGATTCCTGAATCCAGATCTT GGAGGGACGGAGGGTTTTGGTGACAGAGCGAGCGCTAAAATTGAGGATTCCTGAATCCAGATCTT T G CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:8852976..8853050 32194978 MeRIP-seq:(Medium) rs1223585958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481822,Human_RBP_ID_6546604,Human_RBP_ID_12851086,Human_RBP_ID_18288290 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176162 73467 RMVar_ID_73467 Human_SNP_ID_593748504 m1A Human chr16 - 8853425 8853423 8853425 AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCATTGTTTCCTCGCCTGCGATGCTCCTTGTACAT AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCGTAGTTTCCTCGCCTGCGATGCTCCTTGTACAT AAT TAC CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs796559801 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_1283978 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176162 73468 RMVar_ID_73468 Human_SNP_ID_593748509 m1A Human chr16 - 8853425 8853425 8853425 AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCATTGTTTCCTCGCCTGCGATGCTCCTTGTACAT AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCTTTGTTTCCTCGCCTGCGATGCTCCTTGTACAT T A CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283978 GWAS_ID_8910,GWAS_ID_8911,GWAS_ID_8912,GWAS_ID_8913,GWAS_ID_8914,GWAS_ID_8915 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176162 73469 RMVar_ID_73469 Human_SNP_ID_593748510 m1A Human chr16 - 8853425 8853425 8853425 AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCATTGTTTCCTCGCCTGCGATGCTCCTTGTACAT AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCGTTGTTTCCTCGCCTGCGATGCTCCTTGTACAT T C CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283978 GWAS_ID_8910,GWAS_ID_8911,GWAS_ID_8912,GWAS_ID_8913,GWAS_ID_8914,GWAS_ID_8915 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176162 73470 RMVar_ID_73470 Human_SNP_ID_593748511 m1A Human chr16 - 8853425 8853425 8853425 AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCATTGTTTCCTCGCCTGCGATGCTCCTTGTACAT AAGGCAGTTCCCACCACAGTTAGGTCCTGGCCCTTGTTTCCTCGCCTGCGATGCTCCTTGTACAT T G CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283978 GWAS_ID_8910,GWAS_ID_8911,GWAS_ID_8912,GWAS_ID_8913,GWAS_ID_8914,GWAS_ID_8915 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176162 73471 RMVar_ID_73471 Human_SNP_ID_593749364 m1A Human chr16 - 8855110 8855110 8855110 GTCCTGTGCTTGTGGGAGACTTTGCAGGGAGGAGGCAGCAGACACTGGAGATGACATTCTTCCAC GTCCTGTGCTTGTGGGAGACTTTGCAGGGAGGCGGCAGCAGACACTGGAGATGACATTCTTCCAC T G CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:8854968..8855184 26863196 MeRIP-seq:(Medium) rs773740680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089202,Human_RBP_ID_5113861,Human_RBP_ID_17652916,Human_RBP_ID_18189874,Human_RBP_ID_22052935,Human_RBP_ID_26444392 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_109123,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176165,RMVar_hsa_circ_79815,RMVar_hsa_circ_176166,RMVar_hsa_circ_176164,RMVar_hsa_circ_176167,RMVar_hsa_circ_176162 73472 RMVar_ID_73472 Human_SNP_ID_593751185 m1A Human chr16 + 8858094 8858093 8858095 ACACACAAAACCTTACACACCCATTCACAAAGACACACCCAGGGACAATCACAAGTACCGTGTCG ACACACAAAACCTTACACACCCATTCACAAAG__ACACCCAGGGACAATCACAAGTACCGTGTCG GAC G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8858092..8858339 26863196 MeRIP-seq:(Medium) rs1183572936 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1525678 73473 RMVar_ID_73473 Human_SNP_ID_593751439 m1A Human chr16 + 8858460 8858460 8858460 TTGCAGACTCCTTTGTAGACGGGGCCCTGTGAAGCCCGCACCGTCCTGACAGAGAGGGGGAAATG TTGCAGACTCCTTTGTAGACGGGGCCCTGTGAGGCCCGCACCGTCCTGACAGAGAGGGGGAAATG A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8858410..8858514 26863196 MeRIP-seq:(Medium) rs781391215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12853454,Human_RBP_ID_22714272,Human_RBP_ID_26780179 73474 RMVar_ID_73474 Human_SNP_ID_593752070 m1A Human chr16 + 8859322 8859322 8859322 GGTGGGGGGCTGTGGTGGTGGGGGAGGCTCAGATGACATGGCTGACCTGGAAAGAGAAGAGGCTG GGTGGGGGGCTGTGGTGGTGGGGGAGGCTCAGGTGACATGGCTGACCTGGAAAGAGAAGAGGCTG A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:8859176..8859350 26863196 MeRIP-seq:(Medium) rs1567184839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3506925,Human_RBP_ID_5573648,Human_RBP_ID_8188818,Human_RBP_ID_12853816,Human_RBP_ID_22355947,Human_RBP_ID_22713017 73475 RMVar_ID_73475 Human_SNP_ID_593752073 m1A Human chr16 - 8859328 8859328 8859328 CCCTGACAGCCTCTTCTCTTTCCAGGTCAGCCATGTCATCTGAGCCTCCCCCACCACCACAGCCC CCCTGACAGCCTCTTCTCTTTCCAGGTCAGCCGTGTCATCTGAGCCTCCCCCACCACCACAGCCC T C CARHSP1 Ensembl:ENSG00000153048 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:8859226..8859350;chr16:8859201..8859350 26863196 MeRIP-seq:(Medium) rs1238468630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_894132,Human_RBP_ID_4393595,Human_RBP_ID_18189875,Human_RBP_ID_26809971 Human_Splice_Rec_1675814,Human_Splice_Rec_1675826,Human_Splice_Rec_1675832,Human_Splice_Rec_1675840,Human_Splice_Rec_1675848,Human_Splice_Rec_1675854,Human_Splice_Rec_1675860,Human_Splice_Rec_1675866,Human_Splice_Rec_1675874,Human_Splice_Rec_1675880,Human_Splice_Rec_1675888,Human_Splice_Rec_1675894,Human_Splice_Rec_1675904,Human_Splice_Rec_1675906,Human_Splice_Rec_1675912,Human_Splice_Rec_1675918,Human_Splice_Rec_1675920,Human_Splice_Rec_1675922 Human_miRNA_ID_2270006,Human_miRNA_ID_2270007,Human_miRNA_ID_2270008 RMVar_hsa_circ_176163,RMVar_hsa_circ_96504,RMVar_hsa_circ_116897,RMVar_hsa_circ_103775,RMVar_hsa_circ_176164,RMVar_hsa_circ_176167,RMVar_hsa_circ_176162,RMVar_hsa_circ_270618,RMVar_hsa_circ_111484,RMVar_hsa_circ_176170,RMVar_hsa_circ_176171 73476 RMVar_ID_73476 Human_SNP_ID_593756304 m1A Human chr16 - 8868456 8868456 8868456 CCTGGCGCCGCGCGATTAGCCGCATCTGGGGGAGGAGGAGCCGCCGGGCGCGCTGGGCCCGGGTG CCTGGCGCCGCGCGATTAGCCGCATCTGGGGGTGGAGGAGCCGCCGGGCGCGCTGGGCCCGGGTG T A CARHSP1 Ensembl:ENSG00000153048 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:8868449..8868627 26863196 MeRIP-seq:(Medium) rs1567192704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818332,Human_RBP_ID_3502542,Human_RBP_ID_5357609,Human_RBP_ID_8184353,Human_RBP_ID_18459030,Human_RBP_ID_18938766,Human_RBP_ID_22355949,Human_RBP_ID_22415354,Human_RBP_ID_22714280,Human_RBP_ID_26779440 RMVar_hsa_circ_116897,RMVar_hsa_circ_176162 73477 RMVar_ID_73477 Human_SNP_ID_593756478 m1A Human chr16 - 8868909 8868909 8868909 CAGGATAGGCGCCCCTGGCCCGCGGCCCCGGGAGCCGCAGGGGTGGGGCCTCGGCCTCCTCTGCC CAGGATAGGCGCCCCTGGCCCGCGGCCCCGGGTGCCGCAGGGGTGGGGCCTCGGCCTCCTCTGCC T A CARHSP1 Ensembl:ENSG00000153048 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:8868905..8869000;chr16:8868908..8869025 26863196 MeRIP-seq:(Medium) rs1399782042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895524,Human_RBP_ID_3504325,Human_RBP_ID_8231551,Human_RBP_ID_18418921,Human_RBP_ID_18938769 RMVar_hsa_circ_116897,RMVar_hsa_circ_176162 73478 RMVar_ID_73478 Human_SNP_ID_593778744 m1A Human chr16 - 8930399 8930399 8930399 TAAAACCCGTGGAATTTCTTTTTCTTCTTTAAAGCGGGAGATACAGATGACCCACCAAGAATTAC TAAAACCCGTGGAATTTCTTTTTCTTCTTTAATGCGGGAGATACAGATGACCCACCAAGAATTAC T A USP7 Ensembl:ENSG00000187555 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:8930379..8930464 26863196 MeRIP-seq:(Medium) rs1186993204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889453 73479 RMVar_ID_73479 Human_SNP_ID_593790657 m1A Human chr16 + 8963356 8963356 8963356 GGGGCTGCGAGCCCGGCGGGCGGGCGGCGGCGAGCCGGGGCGGCGGCGGCGGCGGCGGCGGCGGG GGGGCTGCGAGCCCGGCGGGCGGGCGGCGGCGGGCCGGGGCGGCGGCGGCGGCGGCGGCGGCGGG A G AC022167.3 Ensembl:ENSG00000260979 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr16:8963261..8963425;chr16:8963201..8963522 26863196 MeRIP-seq:(Medium) rs1328482691 Functional Loss SNV dbSNP153 33..33 33 - - - 73480 RMVar_ID_73480 Human_SNP_ID_593790847 m1A Human chr16 - 8963717 8963717 8963717 CCCCAGGGCCCGCAGGCCCGCCGCGGCCGGCCAGGCCTCCCGTCCGCCGCGCCCGGCCCGAGGCG CCCCAGGGCCCGCAGGCCCGCCGCGGCCGGCCGGGCCTCCCGTCCGCCGCGCCCGGCCCGAGGCG T C USP7 Ensembl:ENSG00000187555 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:8963676..8963900 26863196 MeRIP-seq:(Medium) rs1341808227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394380,Human_RBP_ID_5236547,Human_RBP_ID_9285649,Human_RBP_ID_22441288,Human_RBP_ID_22532671 73481 RMVar_ID_73481 Human_SNP_ID_593834593 m1A Human chr16 + 9091700 9091700 9091700 GGTGCAGGCCGAGCTGCGCGGAGGGCTCGGCGATCAGCGGCGGCGGCGGCAGTGGGGAGGCCGCA GGTGCAGGCCGAGCTGCGCGGAGGGCTCGGCGCTCAGCGGCGGCGGCGGCAGTGGGGAGGCCGCA A C C16orf72 Ensembl:ENSG00000182831 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr16:9091601..9093000;chr16:9091626..9092100;chr16:9091601..9092286 26863196 MeRIP-seq:(Medium) rs1192182146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947256,Human_RBP_ID_4392855,Human_RBP_ID_9325862,Human_RBP_ID_9353095,Human_RBP_ID_18418660,Human_RBP_ID_18469666,Human_RBP_ID_22052940,Human_RBP_ID_22944390,Human_RBP_ID_26329768,Human_RBP_ID_27811588 73482 RMVar_ID_73482 Human_SNP_ID_593834657 m1A Human chr16 - 9091827 9091827 9091827 AACCAGGGACGACCCCCGCCCCAGGCCTTCCCACCCCCGGGCCCGGCCGAAGGTCGCCGCGGACC AACCAGGGACGACCCCCGCCCCAGGCCTTCCCCCCCCCGGGCCCGGCCGAAGGTCGCCGCGGACC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:9091743..9091948 26863410 MeRIP-seq:(Medium) rs1043005290 Functional Loss SNV dbSNP153 33..33 33 - - - 73483 RMVar_ID_73483 Human_SNP_ID_593839182 m1A Human chr16 - 9103751 9103745 9103752 TTAAAGTGCAAGGGACCTGAGGGACGACAGGCAGAAGGTCAAGTCTTACATCCATCCTCTCCCAC TTAAAGTGCAAGGGACCTGAGGGACGACAGG_______TCAAGTCTTACATCCATCCTCTCCCAC ACCTTCTG A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:9103701..9103875 32194978 MeRIP-seq:(Medium) rs1237631552 Functional Loss DEL dbSNP153 32..38 33 - - - 73484 RMVar_ID_73484 Human_SNP_ID_593839184 m1A Human chr16 - 9103751 9103751 9103751 TTAAAGTGCAAGGGACCTGAGGGACGACAGGCAGAAGGTCAAGTCTTACATCCATCCTCTCCCAC TTAAAGTGCAAGGGACCTGAGGGACGACAGGCGGAAGGTCAAGTCTTACATCCATCCTCTCCCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:9103701..9103875 32194978 MeRIP-seq:(Medium) rs191068324 Functional Loss SNV dbSNP153 33..33 33 - - - 73485 RMVar_ID_73485 Human_SNP_ID_593841095 m1A Human chr16 + 9109378 9109378 9109378 AGGGTGGGGAGCCCGATGCCAAGTCAGACTTCACTCGGTATGTTTATTCAAAGCCCCACTTTCAC AGGGTGGGGAGCCCGATGCCAAGTCAGACTTCCCTCGGTATGTTTATTCAAAGCCCCACTTTCAC A C C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:9109176..9109463 26863196 MeRIP-seq:(Medium) rs550633735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5289506,Human_RBP_ID_5573851,Human_RBP_ID_8811541,Human_RBP_ID_12866531,Human_RBP_ID_17255754,Human_RBP_ID_17371148,Human_RBP_ID_17488130,Human_RBP_ID_17883204,Human_RBP_ID_18288466,Human_RBP_ID_27661353 73486 RMVar_ID_73486 Human_SNP_ID_594295040 m1A Human chr16 + 10547600 10547600 10547600 GCTGCAGAGGTGATGTGGAAGGCGATGATGAAAGCAAGAAGCACCAACATTTTCACAGGGCAGGG GCTGCAGAGGTGATGTGGAAGGCGATGATGAATGCAAGAAGCACCAACATTTTCACAGGGCAGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:10547551..10559005 26863196 MeRIP-seq:(Medium) rs1314445387 Functional Loss SNV dbSNP153 33..33 33 - - - 73487 RMVar_ID_73487 Human_SNP_ID_594295045 m1A Human chr16 + 10547622 10547621 10547622 CGATGATGAAAGCAAGAAGCACCAACATTTTCACAGGGCAGGGCGAGTCGAGGCGAGGGGTCACG CGATGATGAAAGCAAGAAGCACCAACATTTTC_CAGGGCAGGGCGAGTCGAGGCGAGGGGTCACG CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:10547551..10547728 26863196 MeRIP-seq:(Medium) rs762760334 Functional Loss DEL dbSNP153 33..33 33 - - - 73488 RMVar_ID_73488 Human_SNP_ID_594295062 m1A Human chr16 + 10547635 10547635 10547635 AAGAAGCACCAACATTTTCACAGGGCAGGGCGAGTCGAGGCGAGGGGTCACGTTTAAAGCCCAGA AAGAAGCACCAACATTTTCACAGGGCAGGGCGCGTCGAGGCGAGGGGTCACGTTTAAAGCCCAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10547551..10547716 26863196 MeRIP-seq:(Medium) rs775951091 Functional Loss SNV dbSNP153 33..33 33 - - - 73489 RMVar_ID_73489 Human_SNP_ID_594295076 m1A Human chr16 - 10547650 10547650 10547650 TTCAGCACATCCCGCTCTGGGCTTTAAACGTGACCCCTCGCCTCGACTCGCCCTGCCCTGTGAAA TTCAGCACATCCCGCTCTGGGCTTTAAACGTGGCCCCTCGCCTCGACTCGCCCTGCCCTGTGAAA T C EMP2 Ensembl:ENSG00000213853 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:10547601..10547700 26863196 MeRIP-seq:(Medium) rs751936119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_467911,Human_RBP_ID_894764,Human_RBP_ID_4392863,Human_RBP_ID_22441293 Human_Splice_Rec_1677000,Human_Splice_Rec_1677008,Human_Splice_Rec_1677016 Human_miRNA_ID_2153619,Human_miRNA_ID_2801496,Human_miRNA_ID_3009629 RMVar_hsa_circ_101300,RMVar_hsa_circ_354564,RMVar_hsa_circ_301051,RMVar_hsa_circ_176201,RMVar_hsa_circ_80066,RMVar_hsa_circ_176200 73490 RMVar_ID_73490 Human_SNP_ID_594295091 m1A Human chr16 - 10547674 10547674 10547674 TTTGAATTTCTCTTTCTTACCCTCTTCAGCACATCCCGCTCTGGGCTTTAAACGTGACCCCTCGC TTTGAATTTCTCTTTCTTACCCTCTTCAGCACGTCCCGCTCTGGGCTTTAAACGTGACCCCTCGC T C EMP2 Ensembl:ENSG00000213853 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:10547576..10547738 26863410 MeRIP-seq:(Medium) rs1567203882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817708,Human_RBP_ID_894764,Human_RBP_ID_4392864 Human_Splice_Rec_1677000,Human_Splice_Rec_1677008,Human_Splice_Rec_1677016 RMVar_hsa_circ_101300,RMVar_hsa_circ_354564,RMVar_hsa_circ_301051,RMVar_hsa_circ_176201,RMVar_hsa_circ_80066,RMVar_hsa_circ_176200 73491 RMVar_ID_73491 Human_SNP_ID_594304124 m1A Human chr16 - 10577669 10577669 10577669 GTCCGGGTGTCTCAGGAGGGCAGGTGATTGGCAGCAGCAGCTGGAATGAAGGAAGAGGGCAGTTG GTCCGGGTGTCTCAGGAGGGCAGGTGATTGGCGGCAGCAGCTGGAATGAAGGAAGAGGGCAGTTG T C EMP2,AC027277.2 Ensembl:ENSG00000213853,Ensembl:ENSG00000260310 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:10577667..10577872 26863196 MeRIP-seq:(Medium) rs28508127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5575797,Human_RBP_ID_8231794 RMVar_hsa_circ_101300,RMVar_hsa_circ_176201 73492 RMVar_ID_73492 Human_SNP_ID_594305111 m1A Human chr16 + 10580602 10580598 10580603 GCAGCTGGATCGACGGACTGGCTGGGGGTGCGAGGCGAGGCCGCCGGGCTGTTTTGAAGCTCTGG GCAGCTGGATCGACGGACTGGCTGGGGGT_____GCGAGGCCGCCGGGCTGTTTTGAAGCTCTGG TGCGAG T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:10580473..10580650;chr16:10580399..10580650 26863196 MeRIP-seq:(Medium) rs1476554087 Functional Loss DEL dbSNP153 30..34 33 - - - 73493 RMVar_ID_73493 Human_SNP_ID_594305114 m1A Human chr16 + 10580602 10580602 10580602 GCAGCTGGATCGACGGACTGGCTGGGGGTGCGAGGCGAGGCCGCCGGGCTGTTTTGAAGCTCTGG GCAGCTGGATCGACGGACTGGCTGGGGGTGCGGGGCGAGGCCGCCGGGCTGTTTTGAAGCTCTGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:10580473..10580650;chr16:10580399..10580650 26863196 MeRIP-seq:(Medium) rs929217635 Functional Loss SNV dbSNP153 33..33 33 - - - 73494 RMVar_ID_73494 Human_SNP_ID_594328725 m1A Human chr16 - 10654924 10654924 10654924 GGGGGGGGGGGGTGGGGGAGGGGAGGGGGGGGAGACAGGACAGTCCATGGCATGGTGGCAGACAC GGGGGGGGGGGGTGGGGGAGGGGAGGGGGGGGGGACAGGACAGTCCATGGCATGGTGGCAGACAC T C TEKT5 Ensembl:ENSG00000153060 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:10654921..10655048 26863196 MeRIP-seq:(Medium) rs1482321853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176202 73495 RMVar_ID_73495 Human_SNP_ID_594359129 m1A Human chr16 + 10743880 10743880 10743880 CGGCAAAGGCGACGGAATGGAGGAGGTGCCTCACGGTAAGCTCGCGGAGGGGGCGTGGGTCGCGG CGGCAAAGGCGACGGAATGGAGGAGGTGCCTCCCGGTAAGCTCGCGGAGGGGGCGTGGGTCGCGG A C NUBP1 Ensembl:ENSG00000103274 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10743826..10747234 26863196 MeRIP-seq:(Medium) rs372365710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394389,Human_RBP_ID_19070895 Human_Splice_Rec_1677047,Human_Splice_Rec_1677057,Human_Splice_Rec_1677075,Human_Splice_Rec_1677095,Human_Splice_Rec_1677107 73496 RMVar_ID_73496 Human_SNP_ID_594359252 m1A Human chr16 - 10744040 10744040 10744040 TTCTCACCCGTGTCCGGAGTGGCCCCCGCTCCAGAAGCGCACAGCCGCTGGTTGGGGCATCCCTG TTCTCACCCGTGTCCGGAGTGGCCCCCGCTCCCGAAGCGCACAGCCGCTGGTTGGGGCATCCCTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:10743920..10744087 26863196 MeRIP-seq:(Medium) rs1307014574 Functional Loss SNV dbSNP153 33..33 33 - - - 73497 RMVar_ID_73497 Human_SNP_ID_594360245 m1A Human chr16 + 10747226 10747226 10747226 TATTGTCTGGGAAAGGCGGTGTTGGGAAAAGCACATTCAGCGCCCACCTTGCCCATGGCCTAGCA TATTGTCTGGGAAAGGCGGTGTTGGGAAAAGCGCATTCAGCGCCCACCTTGCCCATGGCCTAGCA A G NUBP1 Ensembl:ENSG00000103274 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:10747126..10747300 32194978 MeRIP-seq:(Medium) rs1455169565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22759767 Human_Splice_Rec_1677050,Human_Splice_Rec_1677051,Human_Splice_Rec_1677060,Human_Splice_Rec_1677061,Human_Splice_Rec_1677078,Human_Splice_Rec_1677079,Human_Splice_Rec_1677098,Human_Splice_Rec_1677099,Human_Splice_Rec_1677110,Human_Splice_Rec_1677111 Human_miRNA_ID_2237454,Human_miRNA_ID_2873768,Human_miRNA_ID_2981731 RMVar_hsa_circ_57286,RMVar_hsa_circ_296006,RMVar_hsa_circ_176204,RMVar_hsa_circ_44907 73498 RMVar_ID_73498 Human_SNP_ID_594363280 m1A Human chr16 + 10757921 10757921 10757921 CCTCCGAGATGTGGACTGGGGAGAGGTCGACTACCTCATTGTGGACACCCCACCTGGGACGTCGG CCTCCGAGATGTGGACTGGGGAGAGGTCGACTGCCTCATTGTGGACACCCCACCTGGGACGTCGG A G NUBP1 Ensembl:ENSG00000103274 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:10757826..10757937 26863196 MeRIP-seq:(Medium) rs1201764762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22441779 Human_Splice_Rec_1677056,Human_Splice_Rec_1677068,Human_Splice_Rec_1677086,Human_Splice_Rec_1677102,Human_Splice_Rec_1677116 Human_miRNA_ID_1914795,Human_miRNA_ID_1917244,Human_miRNA_ID_1919696,Human_miRNA_ID_1922154,Human_miRNA_ID_1924609,Human_miRNA_ID_1927060,Human_miRNA_ID_1929509,Human_miRNA_ID_1931963,Human_miRNA_ID_2168689,Human_miRNA_ID_2170212,Human_miRNA_ID_2629791,Human_miRNA_ID_2642905,Human_miRNA_ID_3125645 RMVar_hsa_circ_57286,RMVar_hsa_circ_44907,RMVar_hsa_circ_363883,RMVar_hsa_circ_285224,RMVar_hsa_circ_176206 73499 RMVar_ID_73499 Human_SNP_ID_594364460 m1A Human chr16 + 10761867 10761867 10761867 AGAGTGCCCCTGGATCCGCTCATAGGTGGGTGACCCCAGTGTGGGGCGGCACCTCACTCCTCGGT AGAGTGCCCCTGGATCCGCTCATAGGTGGGTGGCCCCAGTGTGGGGCGGCACCTCACTCCTCGGT A G NUBP1 Ensembl:ENSG00000103274 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:10761865..10762278 26863196 MeRIP-seq:(Medium) rs767419864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363883 73500 RMVar_ID_73500 Human_SNP_ID_594364794 m1A Human chr16 + 10762704 10762702 10762704 AGTGCCGGCTGCACCCATGCCTCGGAACTTCCACTCCATTTGTCAGGGAACCAAGGCCAGTGTGA AGTGCCGGCTGCACCCATGCCTCGGAACTTC__CTCCATTTGTCAGGGAACCAAGGCCAGTGTGA CCA C NUBP1 Ensembl:ENSG00000103274 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:10762700..10763322 26863196 MeRIP-seq:(Medium) rs779266915 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_363883 73501 RMVar_ID_73501 Human_SNP_ID_594366891 m1A Human chr16 + 10769147 10769147 10769147 ATGTTCAGGACCAAGCAGTTACCGAGCGAGGCACTCACTGGGCAGCACATCCAGCCAGACCCGAC ATGTTCAGGACCAAGCAGTTACCGAGCGAGGCCCTCACTGGGCAGCACATCCAGCCAGACCCGAC A C NUBP1 Ensembl:ENSG00000103274 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:10769096..10769189 26863196 MeRIP-seq:(Medium) rs1204265718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17653296 Human_miRNA_ID_1097101 RMVar_hsa_circ_176211 73502 RMVar_ID_73502 Human_SNP_ID_594410510 m1A Human chr16 - 10911248 10911247 10911249 GGAAAGGAAAGAAAGAGGAAAGAAAGAGAGAAAGAAAGAAAGAAGAAAGAAAGAAAAAGAAAGAG GGAAAGGAAAGAAAGAGGAAAGAAAGAGAGA__GAAAGAAAGAAGAAAGAAAGAAAAAGAAAGAG CTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10911197..10911281 26863196 MeRIP-seq:(Medium) rs1230560796 Functional Loss DEL dbSNP153 32..33 33 - - - 73503 RMVar_ID_73503 Human_SNP_ID_594410627 m1A Human chr16 - 10911472 10911469 10911473 GAAAGAGAAAGAAAGAGAATGGAAAGAAAGAAAGAGAAAGGAGAGAAAGGAAAGAAAGAAAAGAA GAAAGAGAAAGAAAGAGAATGGAAAGAAAGA____GAAAGGAGAGAAAGGAAAGAAAGAAAAGAA CTCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10911339..10911546 26863196 MeRIP-seq:(Medium) rs1204864805 Functional Loss DEL dbSNP153 32..35 33 - - - 73504 RMVar_ID_73504 Human_SNP_ID_594410629 m1A Human chr16 - 10911472 10911471 10911473 GAAAGAGAAAGAAAGAGAATGGAAAGAAAGAAAGAGAAAGGAGAGAAAGGAAAGAAAGAAAAGAA GAAAGAGAAAGAAAGAGAATGGAAAGAAAGA__GAGAAAGGAGAGAAAGGAAAGAAAGAAAAGAA CTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10911339..10911546 26863196 MeRIP-seq:(Medium) rs917514532 Functional Loss DEL dbSNP153 32..33 33 - - - 73505 RMVar_ID_73505 Human_SNP_ID_594419251 m1A Human chr16 - 10942252 10942252 10942252 CACGAGGGAGCCGGGCAGCCGCGGGCCACTTCAGGGGGGCCCGCCTCGCCGCCCGGGCGGTCGAG CACGAGGGAGCCGGGCAGCCGCGGGCCACTTCTGGGGGGCCCGCCTCGCCGCCCGGGCGGTCGAG T A DEXI Ensembl:ENSG00000182108 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:10942201..10942394 26863196 MeRIP-seq:(Medium) rs1027770187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392868,Human_RBP_ID_8941326,Human_RBP_ID_17653297,Human_RBP_ID_26937983 Human_miRNA_ID_2295897,Human_miRNA_ID_2452624 RMVar_hsa_circ_124032,RMVar_hsa_circ_176222 73506 RMVar_ID_73506 Human_SNP_ID_594420056 m1A Human chr16 - 10944639 10944612 10944639 CAGCAGAGCGGCCCAGCGCCCGCGGCGGTAGCACAAGCGGAGGATGCGGCGGCGGAGGCGGTGGA CAGCAGAGCGGCCCAGCGCCCGCGGCGGTAGC___________________________GGTGGA CGCCTCCGCCGCCGCATCCTCCGCTTGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:10944588..10944755 26863196 MeRIP-seq:(Medium) rs1567478349 Functional Loss DEL dbSNP153 33..59 33 - - - 73507 RMVar_ID_73507 Human_SNP_ID_594420066 m1A Human chr16 - 10944631 10944631 10944631 CGGCCCAGCGCCCGCGGCGGTAGCACAAGCGGAGGATGCGGCGGCGGAGGCGGTGGAGGAACCGC CGGCCCAGCGCCCGCGGCGGTAGCACAAGCGGCGGATGCGGCGGCGGAGGCGGTGGAGGAACCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:10944576..10944837 26863196 MeRIP-seq:(Medium) rs915027425 Functional Loss SNV dbSNP153 33..33 33 - - - 73508 RMVar_ID_73508 Human_SNP_ID_594420095 m1A Human chr16 + 10944695 10944695 10944695 GCTCTGCTGGTCCGGCATGAGACCGTGAGACGAGAGACGGGTCGGGGCCGCCGACATGTTTGGCC GCTCTGCTGGTCCGGCATGAGACCGTGAGACGGGAGACGGGTCGGGGCCGCCGACATGTTTGGCC A G CLEC16A Ensembl:ENSG00000038532 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:10944601..10944800 26863410 MeRIP-seq:(Medium) rs777251829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_467959,Human_RBP_ID_4393605 73509 RMVar_ID_73509 Human_SNP_ID_594420113 m1A Human chr16 - 10944719 10944719 10944719 CCCCGCCCACCCAGCTCCGCGAGCGGCCAAACATGTCGGCGGCCCCGACCCGTCTCTCGTCTCAC CCCCGCCCACCCAGCTCCGCGAGCGGCCAAACGTGTCGGCGGCCCCGACCCGTCTCTCGTCTCAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:10944576..10944844 26863196 MeRIP-seq:(Medium) rs1239269055 Functional Loss SNV dbSNP153 33..33 33 - - - 73510 RMVar_ID_73510 Human_SNP_ID_594423970 m1A Human chr16 - 10957733 10957733 10957733 AAAAGGAAATTAAAGGTTACCAACTGAAATGCAAGCCAAGTTCCATGACCATTAGCAATATTTTG AAAAGGAAATTAAAGGTTACCAACTGAAATGCCAGCCAAGTTCCATGACCATTAGCAATATTTTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:10957728..10957811 26863196 MeRIP-seq:(Medium) rs750154437 Functional Loss SNV dbSNP153 33..33 33 - - - 73511 RMVar_ID_73511 Human_SNP_ID_594437419 m1A Human chr16 + 11003254 11003254 11003254 CCGAGGATGCCCAAGAAGACGCCGAGAAGGCTAAAGGTACAGAGGGTGGTTCAAAAGGCATCAAG CCGAGGATGCCCAAGAAGACGCCGAGAAGGCTGAAGGTACAGAGGGTGGTTCAAAAGGCATCAAG A G CLEC16A Ensembl:ENSG00000038532 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11003204..11003352 26863196 MeRIP-seq:(Medium) rs957696151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1088258,Human_RBP_ID_5524065,Human_RBP_ID_9372262,Human_RBP_ID_22935635,Human_RBP_ID_24544479,Human_RBP_ID_26328649 Human_Splice_Rec_1677617,Human_Splice_Rec_1677661,Human_Splice_Rec_1677693 RMVar_hsa_circ_14509,RMVar_hsa_circ_96819,RMVar_hsa_circ_348620,RMVar_hsa_circ_11922,RMVar_hsa_circ_99138,RMVar_hsa_circ_57611,RMVar_hsa_circ_176229,RMVar_hsa_circ_269480,RMVar_hsa_circ_45788,RMVar_hsa_circ_33678,RMVar_hsa_circ_120200,RMVar_hsa_circ_266597,RMVar_hsa_circ_119442,RMVar_hsa_circ_176231,RMVar_hsa_circ_118053,RMVar_hsa_circ_176233,RMVar_hsa_circ_76996,RMVar_hsa_circ_82949,RMVar_hsa_circ_176235,RMVar_hsa_circ_176237,RMVar_hsa_circ_176236,RMVar_hsa_circ_176234,RMVar_hsa_circ_293894,RMVar_hsa_circ_346930,RMVar_hsa_circ_94607,RMVar_hsa_circ_176241,RMVar_hsa_circ_176242,RMVar_hsa_circ_176240 73512 RMVar_ID_73512 Human_SNP_ID_594457413 m1A Human chr16 + 11067436 11067436 11067436 TTGAGGGCTGCAGGGGGGGTGTGGGTGCCGAGAAGTGGCGCAGAAGAAGCAAAGGCCCTGGGGCC TTGAGGGCTGCAGGGGGGGTGTGGGTGCCGAGCAGTGGCGCAGAAGAAGCAAAGGCCCTGGGGCC A C CLEC16A Ensembl:ENSG00000038532 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11067410..11067565 26863196 MeRIP-seq:(Medium) rs1360721402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94607,RMVar_hsa_circ_176242,RMVar_hsa_circ_374713,RMVar_hsa_circ_57412,RMVar_hsa_circ_272862,RMVar_hsa_circ_176243,RMVar_hsa_circ_176244,RMVar_hsa_circ_123583,RMVar_hsa_circ_46867,RMVar_hsa_circ_104176,RMVar_hsa_circ_122312,RMVar_hsa_circ_176253,RMVar_hsa_circ_99876,RMVar_hsa_circ_176254,RMVar_hsa_circ_176255,RMVar_hsa_circ_91565,RMVar_hsa_circ_176259,RMVar_hsa_circ_176260,RMVar_hsa_circ_108435,RMVar_hsa_circ_357540,RMVar_hsa_circ_176261 73513 RMVar_ID_73513 Human_SNP_ID_594465197 m1A Human chr16 - 11093616 11093616 11093616 ACCCTCGGCGCCTGGCTGATATTTACTTCTTCAAAAATACGCCCACTTTGCTTTAAGACAGATTC ACCCTCGGCGCCTGGCTGATATTTACTTCTTCGAAAATACGCCCACTTTGCTTTAAGACAGATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11093613..11093795 26863196 MeRIP-seq:(Medium) rs1349918597 Functional Loss SNV dbSNP153 33..33 33 - - - 73514 RMVar_ID_73514 Human_SNP_ID_594493170 m1A Human chr16 + 11180499 11180499 11180499 GAAGAGAAGGAAGGCAGGGTGGAGCGGGGGGAAGACCATCATGGAGAGAAGGACCACAGCATCAG GAAGAGAAGGAAGGCAGGGTGGAGCGGGGGGATGACCATCATGGAGAGAAGGACCACAGCATCAG A T CLEC16A Ensembl:ENSG00000038532 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11180449..11180576 26863196 MeRIP-seq:(Medium) rs1318162031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22355959 RMVar_hsa_circ_110672,RMVar_hsa_circ_176265 73515 RMVar_ID_73515 Human_SNP_ID_594493172 m1A Human chr16 + 11180504 11180504 11180504 GAAGGAAGGCAGGGTGGAGCGGGGGGAAGACCATCATGGAGAGAAGGACCACAGCATCAGGAGAC GAAGGAAGGCAGGGTGGAGCGGGGGGAAGACCGTCATGGAGAGAAGGACCACAGCATCAGGAGAC A G CLEC16A Ensembl:ENSG00000038532 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11180455..11180596 26863196 MeRIP-seq:(Medium) rs942562810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22355959 RMVar_hsa_circ_110672,RMVar_hsa_circ_176265 73516 RMVar_ID_73516 Human_SNP_ID_594517317 m1A Human chr16 - 11255426 11255426 11255426 GGCAGCCGACAATGCAGTCTCCACAGCAGCAGAGCCCCGACGGCGGCCAGAACCTTCCTCCTCTT GGCAGCCGACAATGCAGTCTCCACAGCAGCAGTGCCCCGACGGCGGCCAGAACCTTCCTCCTCTT T A SOCS1 Ensembl:ENSG00000185338 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11255334..11255445 26863196 MeRIP-seq:(Medium) rs755719591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371268 73517 RMVar_ID_73517 Human_SNP_ID_594517318 m1A Human chr16 - 11255426 11255426 11255426 GGCAGCCGACAATGCAGTCTCCACAGCAGCAGAGCCCCGACGGCGGCCAGAACCTTCCTCCTCTT GGCAGCCGACAATGCAGTCTCCACAGCAGCAGGGCCCCGACGGCGGCCAGAACCTTCCTCCTCTT T C SOCS1 Ensembl:ENSG00000185338 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11255334..11255445 26863196 MeRIP-seq:(Medium) rs755719591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371268 73518 RMVar_ID_73518 Human_SNP_ID_594538702 m1A Human chr16 - 11319005 11319005 11319005 AAGTTCACCCCAGGGCCTTTGCACGTGCCGTCACTGCACCCAGGACACTGTTCCCTCTGACATTC AAGTTCACCCCAGGGCCTTTGCACGTGCCGTCGCTGCACCCAGGACACTGTTCCCTCTGACATTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11318824..11319192 26863196 MeRIP-seq:(Medium) rs1415013529 Functional Loss SNV dbSNP153 33..33 33 - - - 73519 RMVar_ID_73519 Human_SNP_ID_594547663 m1A Human chr16 + 11345542 11345542 11345542 GGGGGTGCGGCTTCCGAGGTCGCCGCCACTCAAGGTGCTGGCGGAGCAGCTGCGGCGCGACGCGG GGGGGTGCGGCTTCCGAGGTCGCCGCCACTCATGGTGCTGGCGGAGCAGCTGCGGCGCGACGCGG A T RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:11345449..11345625 26863196 MeRIP-seq:(Medium) rs1299654003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4349895,Human_RBP_ID_17871431,Human_RBP_ID_18459039,Human_RBP_ID_22441294 Human_Splice_Rec_1677817 RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 73520 RMVar_ID_73520 Human_SNP_ID_594547674 m1A Human chr16 + 11345569 11345569 11345569 ACTCAAGGTGCTGGCGGAGCAGCTGCGGCGCGACGCGGAGGGCGGCCCGGGCGCGTGGCGGCTGT ACTCAAGGTGCTGGCGGAGCAGCTGCGGCGCGGCGCGGAGGGCGGCCCGGGCGCGTGGCGGCTGT A G RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr16:11345468..11345656;chr16:11345484..11345758 26863196,26863410 MeRIP-seq:(Medium) rs1251689809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4349896,Human_RBP_ID_22441294 RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 73521 RMVar_ID_73521 Human_SNP_ID_594549334 m1A Human chr16 + 11350653 11350653 11350653 GGGCTTTTCTTCTTTTTCTAGGAAAGTATGTGATGGTGATGGGAGTGGTTCAGGCCTGCAGCCCT GGGCTTTTCTTCTTTTTCTAGGAAAGTATGTGGTGGTGATGGGAGTGGTTCAGGCCTGCAGCCCT A G RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11350626..11350725 26863196 MeRIP-seq:(Medium) rs1395980182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4395761,Human_RBP_ID_17871435,Human_RBP_ID_23677908 Human_Splice_Rec_1677814,Human_Splice_Rec_1677818,Human_Splice_Rec_1677820 Human_miRNA_ID_1388251,Human_miRNA_ID_2214661 RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 73522 RMVar_ID_73522 Human_SNP_ID_594625456 m1A Human chr16 + 11556591 11556591 11556591 GATTCATGCCCTTCCCATCAGGCCCCGTCACAAGCCCCGTAGTTGGCCCAGGCATGGGAGCTGGA GATTCATGCCCTTCCCATCAGGCCCCGTCACAGGCCCCGTAGTTGGCCCAGGCATGGGAGCTGGA A G NONHSAG018610.2 RNACentral:URS00008BE331 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:11556463..11556712 32194978 MeRIP-seq:(Medium) rs938875821 Functional Loss SNV dbSNP153 33..33 33 - - - 73523 RMVar_ID_73523 Human_SNP_ID_594625515 m1A Human chr16 - 11556719 11556719 11556719 TCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCAGGACCTTACCAGGCGGCCACTGGGCCTTCCTC TCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCGGGACCTTACCAGGCGGCCACTGGGCCTTCCTC T C LITAF Ensembl:ENSG00000189067 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11556567..11556750 26863196 MeRIP-seq:(Medium) rs760120748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4350003,Human_RBP_ID_22441785,Human_RBP_ID_24544681 Human_Splice_Rec_1678062,Human_Splice_Rec_1678068,Human_Splice_Rec_1678074,Human_Splice_Rec_1678082,Human_Splice_Rec_1678090,Human_Splice_Rec_1678096,Human_Splice_Rec_1678104,Human_Splice_Rec_1678116,Human_Splice_Rec_1678124,Human_Splice_Rec_1678130,Human_Splice_Rec_1678138,Human_Splice_Rec_1678144,Human_Splice_Rec_1678150,Human_Splice_Rec_1678156,Human_Splice_Rec_1678160,Human_Splice_Rec_1678166,Human_Splice_Rec_1678170,Human_Splice_Rec_1678176 RMVar_hsa_circ_24454,RMVar_hsa_circ_176273,RMVar_hsa_circ_274549,RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 73524 RMVar_ID_73524 Human_SNP_ID_594625522 m1A Human chr16 - 11556737 11556737 11556737 ATTTCTTATCTGGTATGTTCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCAGGACCTTACCAGGC ATTTCTTATCTGGTATGTTCTGTTTCTGTTTTTGGTAAAATGTCGGTTCCAGGACCTTACCAGGC T A LITAF Ensembl:ENSG00000189067 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:11556674..11556775 26863410 MeRIP-seq:(Medium) rs761962106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 73525 RMVar_ID_73525 Human_SNP_ID_594630000 m1A Human chr16 - 11572146 11572146 11572146 CTGGAGGGGCTGAGGACCCAGGCTAAGGCAGGAGGGGGATTTTGTTTTGATCTGTTTATTTGTTT CTGGAGGGGCTGAGGACCCAGGCTAAGGCAGGCGGGGGATTTTGTTTTGATCTGTTTATTTGTTT T G LITAF Ensembl:ENSG00000189067 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11572142..11572279 26863196 MeRIP-seq:(Medium) rs1236275436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 73526 RMVar_ID_73526 Human_SNP_ID_594634433 m1A Human chr16 + 11586511 11586511 11586511 ATTTCTGGAAATCTCAACCTGAGTCACTAGAGAGAATCGCGCCTTTTTCTAAAAAGCCCAGGGGC ATTTCTGGAAATCTCAACCTGAGTCACTAGAGCGAATCGCGCCTTTTTCTAAAAAGCCCAGGGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11586508..11586950 26863196 MeRIP-seq:(Medium) rs916853889 Functional Loss SNV dbSNP153 33..33 33 - - - 73527 RMVar_ID_73527 Human_SNP_ID_594634440 m1A Human chr16 - 11586549 11586549 11586549 CTTCGCGGCCCGCCGCGTCCCCCTCCCCGGAGAGGACGGCCCCTGGGCTTTTTAGAAAAAGGCGC CTTCGCGGCCCGCCGCGTCCCCCTCCCCGGAGGGGACGGCCCCTGGGCTTTTTAGAAAAAGGCGC T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11586547..11586950 26863196 MeRIP-seq:(Medium) rs71388711 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_336 GWAS_ID_8916 RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 73528 RMVar_ID_73528 Human_SNP_ID_594634512 m1A Human chr16 - 11586763 11586762 11586763 CTGAGCCCTTGGCTGGGGCCTCCTGGGATGCCAGGGGGCGCGGGTCGGGTCGCGGGCATCGAGGC CTGAGCCCTTGGCTGGGGCCTCCTGGGATGCC_GGGGGCGCGGGTCGGGTCGCGGGCATCGAGGC CT C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:11586741..11586925 26863196 MeRIP-seq:(Medium) rs1417880913 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5357627,Human_RBP_ID_22054478,Human_RBP_ID_26780199 RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 73529 RMVar_ID_73529 Human_SNP_ID_594634660 m1A Human chr16 - 11587205 11587205 11587205 GGGGCGGACGGGTGGGGCTGGCACCGAGAGGCAGGGGCAGGATAGGAGAGTGGGGGAGACACCAG GGGGCGGACGGGTGGGGCTGGCACCGAGAGGCGGGGGCAGGATAGGAGAGTGGGGGAGACACCAG T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11587016..11587365 26863196 MeRIP-seq:(Medium) rs1263712754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1678089,Human_Splice_Rec_1678149 73530 RMVar_ID_73530 Human_SNP_ID_594682356 m1A Human chr16 + 11742643 11742643 11742643 GGCCAGGGTCGGGCTCGAGCTGAGGCAGTCTGAGCCCGCGGGGCCGCCGCCGCCCCCTCCCTCGT GGCCAGGGTCGGGCTCGAGCTGAGGCAGTCTGGGCCCGCGGGGCCGCCGCCGCCCCCTCCCTCGT A G AC007613.1 Ensembl:ENSG00000262420 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:11742598..11742813 26863196 MeRIP-seq:(Medium) rs1208149757 Functional Loss SNV dbSNP153 33..33 33 - - - 73531 RMVar_ID_73531 Human_SNP_ID_594682407 m1A Human chr16 - 11742700 11742700 11742700 TAATGTCGGAATGCGGAGGCCGCGGCGGCGGCAGCAGCAGCAGCGAGGACGCCGAGGACGAGGGA TAATGTCGGAATGCGGAGGCCGCGGCGGCGGCGGCAGCAGCAGCGAGGACGCCGAGGACGAGGGA T C TXNDC11 Ensembl:ENSG00000153066 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11742458..11742908 26863196 MeRIP-seq:(Medium) rs929252570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392874,Human_RBP_ID_12664532,Human_RBP_ID_18418668,Human_RBP_ID_22441298 73532 RMVar_ID_73532 Human_SNP_ID_594694349 m1A Human chr16 - 11782348 11782348 11782348 TTTAGAAAGTGGATGTGTGGGATAACATGTCCAATGTGTCCGAGGAGAGAAGAAAAAGGCAGCAG TTTAGAAAGTGGATGTGTGGGATAACATGTCCGATGTGTCCGAGGAGAGAAGAAAAAGGCAGCAG T C ZC3H7A Ensembl:ENSG00000122299 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11782298..11782426 26863196 MeRIP-seq:(Medium) rs1251647922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891492,Human_RBP_ID_4350194,Human_RBP_ID_26329784 Human_Splice_Rec_1678275,Human_Splice_Rec_1678344,Human_Splice_Rec_1678345,Human_Splice_Rec_1678392,Human_Splice_Rec_1678393,Human_Splice_Rec_1678464,Human_Splice_Rec_1678465,Human_Splice_Rec_1678478,Human_Splice_Rec_1678479,Human_Splice_Rec_1678486,Human_Splice_Rec_1678487,Human_Splice_Rec_1678494,Human_Splice_Rec_1678495,Human_Splice_Rec_1678502,Human_Splice_Rec_1678503 Human_miRNA_ID_2954276,Human_miRNA_ID_2958020,Human_miRNA_ID_3118449 RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_318473,RMVar_hsa_circ_55662,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_288349,RMVar_hsa_circ_176315,RMVar_hsa_circ_282405,RMVar_hsa_circ_60803,RMVar_hsa_circ_176317,RMVar_hsa_circ_311730,RMVar_hsa_circ_176320 73533 RMVar_ID_73533 Human_SNP_ID_594698742 m1A Human chr16 - 11796342 11796342 11796342 GGACCTTGCCATGCCCAGTACGGTGGCCACTGACCCCCCGCCGTTTGGGACGATGGAGCCCACGA GGACCTTGCCATGCCCAGTACGGTGGCCACTGCCCCCCCGCCGTTTGGGACGATGGAGCCCACGA T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11796329..11796624 26863196 MeRIP-seq:(Medium) rs1048166252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1678492,Human_Splice_Rec_1678500 73534 RMVar_ID_73534 Human_SNP_ID_594699104 m1A Human chr16 + 11797154 11797154 11797154 ACCTGTGGGGACGACGCGCCGGCCGGCGGCAGAAGGCAGGCGGAGGCGGGCGGCGGCAGGCGGGC ACCTGTGGGGACGACGCGCCGGCCGGCGGCAGCAGGCAGGCGGAGGCGGGCGGCGGCAGGCGGGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:11797101..11797225 26863410 MeRIP-seq:(Medium) rs971067639 Functional Loss SNV dbSNP153 33..33 33 - - - 73535 RMVar_ID_73535 Human_SNP_ID_594699124 m1A Human chr16 - 11797192 11797192 11797192 GCGAGCACCCAGGCCCCGCCGCCGCCGCCGCCACCGCTGCCCGCCTGCCGCCGCCCGCCTCCGCC GCGAGCACCCAGGCCCCGCCGCCGCCGCCGCCGCCGCTGCCCGCCTGCCGCCGCCCGCCTCCGCC T C ZC3H7A Ensembl:ENSG00000122299 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:11796888..11797267;chr16:11797083..11797250;chr16:11796321..11797250;chr16:11796341..11797250;chr16:11797076..11797230 26863196 MeRIP-seq:(Medium) rs974889504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234811,Human_RBP_ID_9324947,Human_RBP_ID_22532674 Human_Splice_Rec_1678343,Human_Splice_Rec_1678391,Human_Splice_Rec_1678463,Human_Splice_Rec_1678491 73536 RMVar_ID_73536 Human_SNP_ID_594699561 m1A Human chr16 - 11798242 11798242 11798242 CCCAATTCAGACTCAATGAATGACCCCCTTCCACACAAAACTCCAAATTAAACATGGCGGCCCCC CCCAATTCAGACTCAATGAATGACCCCCTTCCGCACAAAACTCCAAATTAAACATGGCGGCCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:11798125..11798281 26863196 MeRIP-seq:(Medium) rs1204644719 Functional Loss SNV dbSNP153 33..33 33 - - - 73537 RMVar_ID_73537 Human_SNP_ID_594713062 m1A Human chr16 + 11837910 11837910 11837910 TTGGCCTCTGGCTTTTTTGGAGTCTGTCTCGCATCTTTTTTCCCCAGCGAAGGACTTTTTTCCTT TTGGCCTCTGGCTTTTTTGGAGTCTGTCTCGCGTCTTTTTTCCCCAGCGAAGGACTTTTTTCCTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:11837821..11837921 26863410 MeRIP-seq:(Medium) rs772278028 Functional Loss SNV dbSNP153 33..33 33 - - - 73538 RMVar_ID_73538 Human_SNP_ID_594716219 m1A Human chr16 - 11846533 11846533 11846533 TCAAGAGAGATCAATGACTGTATAGGTGGAACAGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG TCAAGAGAGATCAATGACTGTATAGGTGGAACTGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG T A RSL1D1 Ensembl:ENSG00000171490 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8052900 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_45517,Human_RBP_ID_1364916,Human_RBP_ID_1838001,Human_RBP_ID_3491207,Human_RBP_ID_5184227,Human_RBP_ID_5571422,Human_RBP_ID_6493044,Human_RBP_ID_12665627,Human_RBP_ID_17188445,Human_RBP_ID_17252890,Human_RBP_ID_17689600,Human_RBP_ID_17871530,Human_RBP_ID_18672980,Human_RBP_ID_22442366,Human_RBP_ID_26446569,Human_RBP_ID_27236667,Human_RBP_ID_27656268 Human_Splice_Rec_1678536,Human_Splice_Rec_1678537,Human_Splice_Rec_1678550,Human_Splice_Rec_1678551,Human_Splice_Rec_1678574,Human_Splice_Rec_1678575,Human_Splice_Rec_1678603,Human_Splice_Rec_1678614,Human_Splice_Rec_1678615,Human_Splice_Rec_1678628,Human_Splice_Rec_1678636 Human_miRNA_ID_2744050,Human_miRNA_ID_2744051 RMVar_hsa_circ_83192,RMVar_hsa_circ_4236,RMVar_hsa_circ_126224,RMVar_hsa_circ_280181,RMVar_hsa_circ_51417,RMVar_hsa_circ_176322,RMVar_hsa_circ_264984,RMVar_hsa_circ_176323,RMVar_hsa_circ_273603,RMVar_hsa_circ_285418,RMVar_hsa_circ_326366,RMVar_hsa_circ_274815,RMVar_hsa_circ_119873,RMVar_hsa_circ_176325,RMVar_hsa_circ_176327,RMVar_hsa_circ_176328,RMVar_hsa_circ_176329,RMVar_hsa_circ_176326 73539 RMVar_ID_73539 Human_SNP_ID_594716220 m1A Human chr16 - 11846533 11846533 11846533 TCAAGAGAGATCAATGACTGTATAGGTGGAACAGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG TCAAGAGAGATCAATGACTGTATAGGTGGAACGGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG T C RSL1D1 Ensembl:ENSG00000171490 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8052900 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_45517,Human_RBP_ID_1364916,Human_RBP_ID_1838001,Human_RBP_ID_3491207,Human_RBP_ID_5184227,Human_RBP_ID_5571422,Human_RBP_ID_6493044,Human_RBP_ID_12665627,Human_RBP_ID_17188445,Human_RBP_ID_17252890,Human_RBP_ID_17689600,Human_RBP_ID_17871530,Human_RBP_ID_18672980,Human_RBP_ID_22442366,Human_RBP_ID_26446569,Human_RBP_ID_27236667,Human_RBP_ID_27656268 Human_Splice_Rec_1678536,Human_Splice_Rec_1678537,Human_Splice_Rec_1678550,Human_Splice_Rec_1678551,Human_Splice_Rec_1678574,Human_Splice_Rec_1678575,Human_Splice_Rec_1678603,Human_Splice_Rec_1678614,Human_Splice_Rec_1678615,Human_Splice_Rec_1678628,Human_Splice_Rec_1678636 Human_miRNA_ID_2744050,Human_miRNA_ID_2744051 RMVar_hsa_circ_83192,RMVar_hsa_circ_4236,RMVar_hsa_circ_126224,RMVar_hsa_circ_280181,RMVar_hsa_circ_51417,RMVar_hsa_circ_176322,RMVar_hsa_circ_264984,RMVar_hsa_circ_176323,RMVar_hsa_circ_273603,RMVar_hsa_circ_285418,RMVar_hsa_circ_326366,RMVar_hsa_circ_274815,RMVar_hsa_circ_119873,RMVar_hsa_circ_176325,RMVar_hsa_circ_176327,RMVar_hsa_circ_176328,RMVar_hsa_circ_176329,RMVar_hsa_circ_176326 73540 RMVar_ID_73540 Human_SNP_ID_594718126 m1A Human chr16 + 11851497 11851497 11851497 TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGAGGCCGAATCCTCCATCTTGTTTCCACCTCGTG TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGCGGCCGAATCCTCCATCTTGTTTCCACCTCGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:11851451..11851550;chr16:11851451..11851525 26863196 MeRIP-seq:(Medium) rs371371503 Functional Loss SNV dbSNP153 33..33 33 - - - 73541 RMVar_ID_73541 Human_SNP_ID_594718127 m1A Human chr16 + 11851497 11851497 11851497 TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGAGGCCGAATCCTCCATCTTGTTTCCACCTCGTG TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGGGGCCGAATCCTCCATCTTGTTTCCACCTCGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:11851451..11851550;chr16:11851451..11851525 26863196 MeRIP-seq:(Medium) rs371371503 Functional Loss SNV dbSNP153 33..33 33 - - - 73542 RMVar_ID_73542 Human_SNP_ID_594731844 m1A Human chr16 + 11896659 11896659 11896659 TAGGTTTTGGGATTTCCTCTTCCTCCTCCATCATTTCATGGGCACTTTCCTCTGGCGGCCTTCCA TAGGTTTTGGGATTTCCTCTTCCTCCTCCATCTTTTCATGGGCACTTTCCTCTGGCGGCCTTCCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:11896608..11896741 26863196 MeRIP-seq:(Medium) rs1366346216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176359,RMVar_hsa_circ_176360 73543 RMVar_ID_73543 Human_SNP_ID_594737572 m1A Human chr16 - 11915057 11915057 11915057 TACCCACTTGAGATGGGAACCGTATGGAACGGAGTGGGGGCCGCGGCGGATCCCTGCCACGAGGC TACCCACTTGAGATGGGAACCGTATGGAACGGGGTGGGGGCCGCGGCGGATCCCTGCCACGAGGC T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:11915055..11915156 26863196 MeRIP-seq:(Medium) rs748812560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26757748,Human_RBP_ID_27656380 Human_Splice_Rec_1678793,Human_Splice_Rec_1678807 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73544 RMVar_ID_73544 Human_SNP_ID_594737902 m1A Human chr16 - 11915623 11915623 11915623 CAGCAGCGACTCGGCGCCTGACTGCTGGGACCAGGCGGACATGGAAGCCCCCGGGCCGGGCCCTT CAGCAGCGACTCGGCGCCTGACTGCTGGGACCGGGCGGACATGGAAGCCCCCGGGCCGGGCCCTT T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:11915574..11915677 32194978 MeRIP-seq:(Medium) rs1274210487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512376,Human_RBP_ID_6493584,Human_RBP_ID_12667533,Human_RBP_ID_18673057,Human_RBP_ID_22441300,Human_RBP_ID_27155762,Human_RBP_ID_27439042 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73545 RMVar_ID_73545 Human_SNP_ID_594737909 m1A Human chr16 - 11915647 11915647 11915647 CGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCGCCTGACTGCTGGGACCAGGCGGACA CGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGGCTCGGCGCCTGACTGCTGGGACCAGGCGGACA T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11915476..11915975 26863196 MeRIP-seq:(Medium) rs1265790409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233475,Human_RBP_ID_6493584,Human_RBP_ID_9325869,Human_RBP_ID_12667533,Human_RBP_ID_18673057,Human_RBP_ID_22441787 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73546 RMVar_ID_73546 Human_SNP_ID_594737925 m1A Human chr16 - 11915672 11915666 11915673 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCAGCGACTCGGCG TGCTGCTC CGCCGCCG GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:11915570..11915690 26863410 MeRIP-seq:(Medium) rs1555506537 Functional Loss MNV dbSNP153 32..39 33 - - - Human_RBP_ID_233475,Human_RBP_ID_5648359,Human_RBP_ID_9324949,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17669772,Human_RBP_ID_18409386,Human_RBP_ID_22441787,Human_RBP_ID_22532676,Human_RBP_ID_22760640,Human_RBP_ID_24544754 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73547 RMVar_ID_73547 Human_SNP_ID_594737929 m1A Human chr16 - 11915672 11915670 11915673 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG___CAGCAGCGGCAGCAGCAGCAGCGACTCGGCG GCTC G GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:11915570..11915690 26863410 MeRIP-seq:(Medium) rs1180484922 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_233475,Human_RBP_ID_5648359,Human_RBP_ID_9324949,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17669772,Human_RBP_ID_18409386,Human_RBP_ID_22441787,Human_RBP_ID_22532676,Human_RBP_ID_22760640,Human_RBP_ID_24544754 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73548 RMVar_ID_73548 Human_SNP_ID_594737933 m1A Human chr16 - 11915672 11915672 11915672 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:11915570..11915690 26863410 MeRIP-seq:(Medium) rs1189427317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233475,Human_RBP_ID_5648359,Human_RBP_ID_9324949,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17669772,Human_RBP_ID_18409386,Human_RBP_ID_22441787,Human_RBP_ID_22532676,Human_RBP_ID_22760640,Human_RBP_ID_24544754 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73549 RMVar_ID_73549 Human_SNP_ID_594737973 m1A Human chr16 - 11915708 11915699 11915708 CACACACGGCCCCCCCGATCATGGATCCGGGCAGTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CACACACGGCCCCCCCGATCATGGATCCGGGC_________GGCGGCGGCGGCGGCGGCGGCGGC CGCCGCCACT C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:11915426..11915975 26863196 MeRIP-seq:(Medium) rs1439432825 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_892999,Human_RBP_ID_1527252,Human_RBP_ID_3511585,Human_RBP_ID_4350517,Human_RBP_ID_5088228,Human_RBP_ID_8727023,Human_RBP_ID_8812815,Human_RBP_ID_9324949,Human_RBP_ID_17257686,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17586813,Human_RBP_ID_18926690,Human_RBP_ID_19077804,Human_RBP_ID_21959997,Human_RBP_ID_22441787,Human_RBP_ID_22532770,Human_RBP_ID_22655603,Human_RBP_ID_22799860,Human_RBP_ID_22945288 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73550 RMVar_ID_73550 Human_SNP_ID_594737983 m1A Human chr16 - 11915708 11915708 11915708 CACACACGGCCCCCCCGATCATGGATCCGGGCAGTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CACACACGGCCCCCCCGATCATGGATCCGGGCGGTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:11915426..11915975 26863196 MeRIP-seq:(Medium) rs779813678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892999,Human_RBP_ID_1527252,Human_RBP_ID_3511585,Human_RBP_ID_4350517,Human_RBP_ID_5088228,Human_RBP_ID_8727023,Human_RBP_ID_8812815,Human_RBP_ID_9324949,Human_RBP_ID_17257686,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17586813,Human_RBP_ID_18926690,Human_RBP_ID_19077804,Human_RBP_ID_21959997,Human_RBP_ID_22441787,Human_RBP_ID_22532770,Human_RBP_ID_22655603,Human_RBP_ID_22799860,Human_RBP_ID_22945288 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73551 RMVar_ID_73551 Human_SNP_ID_594738020 m1A Human chr16 + 11915749 11915749 11915749 CCATGATCGGGGGGGCCGTGTGTGTGGTGGACAGAGAGCGGGAAATGGAGGCAGGGGCGCCCGGC CCATGATCGGGGGGGCCGTGTGTGTGGTGGACTGAGAGCGGGAAATGGAGGCAGGGGCGCCCGGC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:11915501..11915975 26863196 MeRIP-seq:(Medium) rs919975349 Functional Loss SNV dbSNP153 33..33 33 - - - 73552 RMVar_ID_73552 Human_SNP_ID_594738080 m1A Human chr16 - 11915840 11915840 11915840 CTGCCGCGGCGACGCCGGGGATCTTTGTCGCTAGCTCCCGGCCCTTCTGCCCCGCCGCCTTCCCT CTGCCGCGGCGACGCCGGGGATCTTTGTCGCTGGCTCCCGGCCCTTCTGCCCCGCCGCCTTCCCT T C GSPT1 Ensembl:ENSG00000103342 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:11915609..11915903 26863410 MeRIP-seq:(Medium) rs1188021761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_894325,Human_RBP_ID_4350521,Human_RBP_ID_5418968,Human_RBP_ID_5440127,Human_RBP_ID_9324950,Human_RBP_ID_12667536,Human_RBP_ID_18673062,Human_RBP_ID_22052984,Human_RBP_ID_22532677,Human_RBP_ID_25191282,Human_RBP_ID_27439044 Human_miRNA_ID_3066109 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 73553 RMVar_ID_73553 Human_SNP_ID_594738083 m1A Human chr16 + 11915847 11915847 11915847 GCGGCGGGGCAGAAGGGCCGGGAGCTAGCGACAAAGATCCCCGGCGTCGCCGCGGCAGCAGCTCC GCGGCGGGGCAGAAGGGCCGGGAGCTAGCGACCAAGATCCCCGGCGTCGCCGCGGCAGCAGCTCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:11915426..11915950 26863410 MeRIP-seq:(Medium) rs753537062 Functional Loss SNV dbSNP153 33..33 33 - - - 73554 RMVar_ID_73554 Human_SNP_ID_594780160 m1A Human chr16 - 12046350 12046350 12046350 TGCAGATTGAAAGAGAAAAGGAAATCGTTCTTAGCAGTGGTTCTCTGTGTCCATTAACCAGGAAA TGCAGATTGAAAGAGAAAAGGAAATCGTTCTTGGCAGTGGTTCTCTGTGTCCATTAACCAGGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12046344..12046411 26863196 MeRIP-seq:(Medium) rs754902946 Functional Loss SNV dbSNP153 33..33 33 - - - 73555 RMVar_ID_73555 Human_SNP_ID_594820559 m1A Human chr16 + 12170593 12170593 12170593 GTGGGGCTGTGGGGGTGGAGAAGAATGCTCTGACATGGGACGGAGGCTTCTGGGACTTCTCACGG GTGGGGCTGTGGGGGTGGAGAAGAATGCTCTGCCATGGGACGGAGGCTTCTGGGACTTCTCACGG A C SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12170587..12170806 26863196 MeRIP-seq:(Medium) rs1395870291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3508913,Human_RBP_ID_23678623 RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_74057,RMVar_hsa_circ_100866,RMVar_hsa_circ_306268,RMVar_hsa_circ_176372,RMVar_hsa_circ_316771,RMVar_hsa_circ_128171,RMVar_hsa_circ_176376,RMVar_hsa_circ_114174,RMVar_hsa_circ_5008,RMVar_hsa_circ_363050,RMVar_hsa_circ_176379,RMVar_hsa_circ_88873,RMVar_hsa_circ_30654,RMVar_hsa_circ_176383 73556 RMVar_ID_73556 Human_SNP_ID_594958688 m1A Human chr16 - 12544503 12544503 12544503 CTAGGCCACACAATTCCCCACAGAAAAATGCCATCTAGACCCCAGCCGACCCCAATCATAAAATC CTAGGCCACACAATTCCCCACAGAAAAATGCCGTCTAGACCCCAGCCGACCCCAATCATAAAATC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:12544392..12544519 26863196 MeRIP-seq:(Medium) rs1394979054 Functional Loss SNV dbSNP153 33..33 33 - - - 73557 RMVar_ID_73557 Human_SNP_ID_594981104 m1A Human chr16 + 12568729 12568727 12568729 TGGCCCCTCACCTCAGCGTGACAACCACGTCCACCTGGTGATCCTGAGAGCACACGATTCCCAAC TGGCCCCTCACCTCAGCGTGACAACCACGTC__CCTGGTGATCCTGAGAGCACACGATTCCCAAC CCA C SNX29 Ensembl:ENSG00000048471 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12568679..12568744 26863196 MeRIP-seq:(Medium) rs1215060843 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_88873,RMVar_hsa_circ_176383,RMVar_hsa_circ_176387,RMVar_hsa_circ_95036,RMVar_hsa_circ_176389,RMVar_hsa_circ_113689 73558 RMVar_ID_73558 Human_SNP_ID_594981106 m1A Human chr16 + 12568729 12568728 12568729 TGGCCCCTCACCTCAGCGTGACAACCACGTCCACCTGGTGATCCTGAGAGCACACGATTCCCAAC TGGCCCCTCACCTCAGCGTGACAACCACGTCC_CCTGGTGATCCTGAGAGCACACGATTCCCAAC CA C SNX29 Ensembl:ENSG00000048471 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12568679..12568744 26863196 MeRIP-seq:(Medium) rs879469756 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_88873,RMVar_hsa_circ_176383,RMVar_hsa_circ_176387,RMVar_hsa_circ_95036,RMVar_hsa_circ_176389,RMVar_hsa_circ_113689 73559 RMVar_ID_73559 Human_SNP_ID_594981108 m1A Human chr16 + 12568729 12568729 12568729 TGGCCCCTCACCTCAGCGTGACAACCACGTCCACCTGGTGATCCTGAGAGCACACGATTCCCAAC TGGCCCCTCACCTCAGCGTGACAACCACGTCCCCCTGGTGATCCTGAGAGCACACGATTCCCAAC A C SNX29 Ensembl:ENSG00000048471 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12568679..12568744 26863196 MeRIP-seq:(Medium) rs1075844 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8917,GWAS_ID_8918,GWAS_ID_8919,GWAS_ID_8920 RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_88873,RMVar_hsa_circ_176383,RMVar_hsa_circ_176387,RMVar_hsa_circ_95036,RMVar_hsa_circ_176389,RMVar_hsa_circ_113689 73560 RMVar_ID_73560 Human_SNP_ID_594981109 m1A Human chr16 + 12568729 12568729 12568730 TGGCCCCTCACCTCAGCGTGACAACCACGTCCACCTGGTGATCCTGAGAGCACACGATTCCCAAC TGGCCCCTCACCTCAGCGTGACAACCACGTCCCACTGGTGATCCTGAGAGCACACGATTCCCAAC AC CA SNX29 Ensembl:ENSG00000048471 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12568679..12568744 26863196 MeRIP-seq:(Medium) rs71378365 Functional Loss MNV dbSNP153 33..34 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_88873,RMVar_hsa_circ_176383,RMVar_hsa_circ_176387,RMVar_hsa_circ_95036,RMVar_hsa_circ_176389,RMVar_hsa_circ_113689 73561 RMVar_ID_73561 Human_SNP_ID_595415477 m1A Human chr16 - 13920233 13920233 13920233 CTACTAGCCCGTCAGTGTCGAGCAGTTCCAGCACCAGCTGTCGCTCGTACTCCAGCAGCGGCGCC CTACTAGCCCGTCAGTGTCGAGCAGTTCCAGCCCCAGCTGTCGCTCGTACTCCAGCAGCGGCGCC T G lnc-PARN-13 RNACentral:URS00008B515C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:13920185..13920316 26863196 MeRIP-seq:(Medium) rs1291749487 Functional Loss SNV dbSNP153 33..33 33 - - - 73562 RMVar_ID_73562 Human_SNP_ID_595415502 m1A Human chr16 + 13920261 13920261 13920261 CTGGTGCTGGAACTGCTCGACACTGACGGGCTAGTAGTGTGCGCCCGCGGGCTCGGCGCGGACCG CTGGTGCTGGAACTGCTCGACACTGACGGGCTGGTAGTGTGCGCCCGCGGGCTCGGCGCGGACCG A G ERCC4 Ensembl:ENSG00000175595 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:13920211..13920309 26863196 MeRIP-seq:(Medium) rs772933233 Functional Loss SNV dbSNP153 33..33 33 - - - 73563 RMVar_ID_73563 Human_SNP_ID_595455671 m1A Human chr16 - 14071367 14071367 14071367 CAGCCCCCAACGGCCGCCACCGCCCGCCGCTCACCTCCCCGGCCGCCGCCGCCGCCGCTCCCGCC CAGCCCCCAACGGCCGCCACCGCCCGCCGCTCCCCTCCCCGGCCGCCGCCGCCGCCGCTCCCGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:14071179..14071494;chr16:14071198..14071579 26863196 MeRIP-seq:(Medium) rs903694454 Functional Loss SNV dbSNP153 33..33 33 - - - 73564 RMVar_ID_73564 Human_SNP_ID_595465522 m1A Human chr16 - 14112178 14112178 14112178 CCTGCCACCTTTTTCCTTTCCTACCTCCCTTGATATGGGCTCTTACTCTTTCTGCTTCAGGGTCA CCTGCCACCTTTTTCCTTTCCTACCTCCCTTGTTATGGGCTCTTACTCTTTCTGCTTCAGGGTCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:14112168..14112316 26863196 MeRIP-seq:(Medium) rs572501906 Functional Loss SNV dbSNP153 33..33 33 - - - 73565 RMVar_ID_73565 Human_SNP_ID_595494637 m1A Human chr16 - 14233356 14233356 14233356 CCCGAATGCCCATGCCACCCATGTGTCCATAAATGTGCTTTACACCCTCTGTTCCTCTCTCCAAA CCCGAATGCCCATGCCACCCATGTGTCCATAACTGTGCTTTACACCCTCTGTTCCTCTCTCCAAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:14233353..14233482 26863196 MeRIP-seq:(Medium) rs1274061136 Functional Loss SNV dbSNP153 33..33 33 - - - 73566 RMVar_ID_73566 Human_SNP_ID_595509340 m1A Human chr16 - 14286009 14286009 14286009 AAGGATCTACTCGCAGAGTACGGCAAGAGTCGACCACTCCTAAAAAGTCTCCACCCTATAGCTGA AAGGATCTACTCGCAGAGTACGGCAAGAGTCGCCCACTCCTAAAAAGTCTCCACCCTATAGCTGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:14285935..14286086 26863196 MeRIP-seq:(Medium) rs1253389320 Functional Loss SNV dbSNP153 33..33 33 - - - 73567 RMVar_ID_73567 Human_SNP_ID_595509346 m1A Human chr16 - 14286014 14286014 14286014 GGGGGAAGGATCTACTCGCAGAGTACGGCAAGAGTCGACCACTCCTAAAAAGTCTCCACCCTATA GGGGGAAGGATCTACTCGCAGAGTACGGCAAGGGTCGACCACTCCTAAAAAGTCTCCACCCTATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:14285862..14286056 26863196 MeRIP-seq:(Medium) rs1441055551 Functional Loss SNV dbSNP153 33..33 33 - - - 73568 RMVar_ID_73568 Human_SNP_ID_595523872 m1A Human chr16 + 14338434 14338411 14338435 ATCCATCCACCCACCTACCCATCCATCCACCCATCCACCTACCCATCCATCCACCCATCTACCTA ATCCATCCAC________________________CCACCTACCCATCCATCCACCCATCTACCTA CCCACCTACCCATCCATCCACCCAT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:14338306..14338433 26863196 MeRIP-seq:(Medium) rs1169179944 Functional Loss DEL dbSNP153 11..34 33 - - - 73569 RMVar_ID_73569 Human_SNP_ID_595523879 m1A Human chr16 + 14338434 14338431 14338435 ATCCATCCACCCACCTACCCATCCATCCACCCATCCACCTACCCATCCATCCACCCATCTACCTA ATCCATCCACCCACCTACCCATCCATCCAC____CCACCTACCCATCCATCCACCCATCTACCTA CCCAT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:14338306..14338433 26863196 MeRIP-seq:(Medium) rs1395686319 Functional Loss DEL dbSNP153 31..34 33 - - - 73570 RMVar_ID_73570 Human_SNP_ID_595523880 m1A Human chr16 + 14338434 14338434 14338434 ATCCATCCACCCACCTACCCATCCATCCACCCATCCACCTACCCATCCATCCACCCATCTACCTA ATCCATCCACCCACCTACCCATCCATCCACCCGTCCACCTACCCATCCATCCACCCATCTACCTA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:14338306..14338433 26863196 MeRIP-seq:(Medium) rs1409027695 Functional Loss SNV dbSNP153 33..33 33 - - - 73571 RMVar_ID_73571 Human_SNP_ID_595568254 m1A Human chr16 - 14508868 14508868 14508868 AAATTAAGAGACTGGGTCTTGCTGTGTTGCCCAGGCTAGTCTTGAACTCCTGGCCTCAAGTGATC AAATTAAGAGACTGGGTCTTGCTGTGTTGCCCTGGCTAGTCTTGAACTCCTGGCCTCAAGTGATC T A PARN Ensembl:ENSG00000140694 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:14508740..14508883 26863196 MeRIP-seq:(Medium) rs1474712427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81827,RMVar_hsa_circ_176423,RMVar_hsa_circ_176421,RMVar_hsa_circ_336947,RMVar_hsa_circ_378040,RMVar_hsa_circ_68448,RMVar_hsa_circ_176422 73572 RMVar_ID_73572 Human_SNP_ID_595592910 m1A Human chr16 - 14602372 14602372 14602372 ATTGTCATTGGCAGAGAGACTGGGACTGGATCAGAGCAACTGCAGAGTACGTGAGGAATGAGAAG ATTGTCATTGGCAGAGAGACTGGGACTGGATCGGAGCAACTGCAGAGTACGTGAGGAATGAGAAG T C PARN Ensembl:ENSG00000140694 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:14602368..14602492 26863196 MeRIP-seq:(Medium) rs933457597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12670917 RMVar_hsa_circ_837,RMVar_hsa_circ_69205,RMVar_hsa_circ_81827,RMVar_hsa_circ_176421,RMVar_hsa_circ_68448,RMVar_hsa_circ_370001,RMVar_hsa_circ_317954,RMVar_hsa_circ_176424,RMVar_hsa_circ_377783,RMVar_hsa_circ_291863,RMVar_hsa_circ_292883,RMVar_hsa_circ_287840,RMVar_hsa_circ_176433,RMVar_hsa_circ_176435,RMVar_hsa_circ_176436,RMVar_hsa_circ_176434,RMVar_hsa_circ_338767,RMVar_hsa_circ_176441,RMVar_hsa_circ_119671,RMVar_hsa_circ_176437,RMVar_hsa_circ_315664,RMVar_hsa_circ_363503,RMVar_hsa_circ_291003,RMVar_hsa_circ_275170,RMVar_hsa_circ_176443,RMVar_hsa_circ_176445,RMVar_hsa_circ_86233,RMVar_hsa_circ_176444,RMVar_hsa_circ_176442,RMVar_hsa_circ_19051,RMVar_hsa_circ_108695,RMVar_hsa_circ_345983,RMVar_hsa_circ_364338,RMVar_hsa_circ_276029,RMVar_hsa_circ_176447,RMVar_hsa_circ_176449,RMVar_hsa_circ_66654,RMVar_hsa_circ_176448,RMVar_hsa_circ_319240,RMVar_hsa_circ_378579,RMVar_hsa_circ_176446,RMVar_hsa_circ_364974,RMVar_hsa_circ_274807,RMVar_hsa_circ_176450,RMVar_hsa_circ_176451,RMVar_hsa_circ_176452 73573 RMVar_ID_73573 Human_SNP_ID_595601210 m1A Human chr16 - 14630147 14630147 14630147 CCGCTGAGGCGGGCGCGGGCCCGGGTGGGGCCAAGGTTCCGGCCACTCTGCAGAATGGAGATAAT CCGCTGAGGCGGGCGCGGGCCCGGGTGGGGCCGAGGTTCCGGCCACTCTGCAGAATGGAGATAAT T C PARN Ensembl:ENSG00000140694 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:14630101..14630225 26863410 MeRIP-seq:(Medium) rs1187518206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393615,Human_RBP_ID_5465836,Human_RBP_ID_17883383,Human_RBP_ID_18418672 Human_Splice_Rec_1679469,Human_Splice_Rec_1679511,Human_Splice_Rec_1679555,Human_Splice_Rec_1679601,Human_Splice_Rec_1679687,Human_Splice_Rec_1679725,Human_Splice_Rec_1679809,Human_Splice_Rec_1679853,Human_Splice_Rec_1679897,Human_Splice_Rec_1679985,Human_Splice_Rec_1680019,Human_Splice_Rec_1680061,Human_Splice_Rec_1680105,Human_Splice_Rec_1680147,Human_Splice_Rec_1680197,Human_Splice_Rec_1680237,Human_Splice_Rec_1680277,Human_Splice_Rec_1680355,Human_Splice_Rec_1680431,Human_Splice_Rec_1680453,Human_Splice_Rec_1680475 73574 RMVar_ID_73574 Human_SNP_ID_595601215 m1A Human chr16 + 14630154 14630154 14630154 CCATTCTGCAGAGTGGCCGGAACCTTGGCCCCACCCGGGCCCGCGCCCGCCTCAGCGGTTCTACT CCATTCTGCAGAGTGGCCGGAACCTTGGCCCCCCCCGGGCCCGCGCCCGCCTCAGCGGTTCTACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:14630114..14630211;chr16:14629634..14630217;chr16:14630113..14630203 26863196 MeRIP-seq:(Medium) rs761271672 Functional Loss SNV dbSNP153 33..33 33 - - - 73575 RMVar_ID_73575 Human_SNP_ID_595601216 m1A Human chr16 + 14630154 14630154 14630154 CCATTCTGCAGAGTGGCCGGAACCTTGGCCCCACCCGGGCCCGCGCCCGCCTCAGCGGTTCTACT CCATTCTGCAGAGTGGCCGGAACCTTGGCCCCTCCCGGGCCCGCGCCCGCCTCAGCGGTTCTACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:14630114..14630211;chr16:14629634..14630217;chr16:14630113..14630203 26863196 MeRIP-seq:(Medium) rs761271672 Functional Loss SNV dbSNP153 33..33 33 - - - 73576 RMVar_ID_73576 Human_SNP_ID_595606685 m1A Human chr16 - 14648514 14648514 14648514 CCCATCTGCTGATTCGCTCGGCCTGTGTTAGGAGCTAAAGGAATCTGATCATTCCCATATTTCTG CCCATCTGCTGATTCGCTCGGCCTGTGTTAGGGGCTAAAGGAATCTGATCATTCCCATATTTCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14648465..14648565 32194978 MeRIP-seq:(Medium) rs775080880 Functional Loss SNV dbSNP153 33..33 33 - - - 73577 RMVar_ID_73577 Human_SNP_ID_595608584 m1A Human chr16 + 14655110 14655110 14655110 TTTGACAGAGGAAGAATTTTCCAAGACGCCCTATACCATAGAAAACAGCAGCCACAGGAGAGCCA TTTGACAGAGGAAGAATTTTCCAAGACGCCCTGTACCATAGAAAACAGCAGCCACAGGAGAGCCA A G BFAR Ensembl:ENSG00000103429 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14655092..14665022 32194978 MeRIP-seq:(Medium) rs370231919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44536,Human_RBP_ID_1281006,Human_RBP_ID_1838331,Human_RBP_ID_8428050,Human_RBP_ID_17871981,Human_RBP_ID_22799895,Human_RBP_ID_26636179 Human_Splice_Rec_1680494,Human_Splice_Rec_1680512,Human_Splice_Rec_1680520,Human_Splice_Rec_1680538 RMVar_hsa_circ_176462,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461,RMVar_hsa_circ_5361,RMVar_hsa_circ_267338,RMVar_hsa_circ_176468,RMVar_hsa_circ_111467,RMVar_hsa_circ_176467,RMVar_hsa_circ_176470,RMVar_hsa_circ_334196,RMVar_hsa_circ_372841,RMVar_hsa_circ_331449,RMVar_hsa_circ_176469 73578 RMVar_ID_73578 Human_SNP_ID_595612563 m1A Human chr16 + 14668841 14668835 14668842 CTGGGTGACAGAGGGAGACTCTGTCTTAAAAAAAAAAAAAAAATCATCTGTAAAATAAATTCCGG CTGGGTGACAGAGGGAGACTCTGTCTT_______AAAAAAAAATCATCTGTAAAATAAATTCCGG TAAAAAAA T BFAR Ensembl:ENSG00000103429 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14668790..14668939 32194978 MeRIP-seq:(Medium) rs528596737 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_21888502 73579 RMVar_ID_73579 Human_SNP_ID_595612564 m1A Human chr16 + 14668841 14668835 14668842 CTGGGTGACAGAGGGAGACTCTGTCTTAAAAAAAAAAAAAAAATCATCTGTAAAATAAATTCCGG CTGGGTGACAGAGGGAGACTCTGTCTTAAA____AAAAAAAAATCATCTGTAAAATAAATTCCGG TAAAAAAA TAAA BFAR Ensembl:ENSG00000103429 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14668790..14668939 32194978 MeRIP-seq:(Medium) rs528596737 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_21888502 73580 RMVar_ID_73580 Human_SNP_ID_595612565 m1A Human chr16 + 14668841 14668835 14668842 CTGGGTGACAGAGGGAGACTCTGTCTTAAAAAAAAAAAAAAAATCATCTGTAAAATAAATTCCGG CTGGGTGACAGAGGGAGACTCTGTCTTAAAA___AAAAAAAAATCATCTGTAAAATAAATTCCGG TAAAAAAA TAAAA BFAR Ensembl:ENSG00000103429 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14668790..14668939 32194978 MeRIP-seq:(Medium) rs528596737 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_21888502 73581 RMVar_ID_73581 Human_SNP_ID_595612566 m1A Human chr16 + 14668841 14668835 14668842 CTGGGTGACAGAGGGAGACTCTGTCTTAAAAAAAAAAAAAAAATCATCTGTAAAATAAATTCCGG CTGGGTGACAGAGGGAGACTCTGTCTTAAAAA__AAAAAAAAATCATCTGTAAAATAAATTCCGG TAAAAAAA TAAAAA BFAR Ensembl:ENSG00000103429 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14668790..14668939 32194978 MeRIP-seq:(Medium) rs528596737 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_21888502 73582 RMVar_ID_73582 Human_SNP_ID_595620550 m1A Human chr16 + 14764032 14764032 14764032 TGTACCTTCAAAAGCTGCCGAGTCCTATGATTACACGCGATGGGACTTGTACACTTGAAGTGAAA TGTACCTTCAAAAGCTGCCGAGTCCTATGATTGCACGCGATGGGACTTGTACACTTGAAGTGAAA A G NPIPA2 Ensembl:ENSG00000254852 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1555520472 Functional Loss SNV dbSNP153 33..33 33 - - - 73583 RMVar_ID_73583 Human_SNP_ID_595652741 m1A Human chr16 + 14912034 14912034 14912034 AGGACGCTCCCAGGGCGAGGCTCCGGCGCAGCACAGCGGCCCTGCTAAATAAGGAACGCCTGGAG AGGACGCTCCCAGGGCGAGGCTCCGGCGCAGCGCAGCGGCCCTGCTAAATAAGGAACGCCTGGAG A G AC138932.1 Ensembl:ENSG00000183458 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:14911989..14912064 26863196 MeRIP-seq:(Medium) rs1356587717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891519,Human_RBP_ID_3506960,Human_RBP_ID_5357647,Human_RBP_ID_8188154,Human_RBP_ID_9422039,Human_RBP_ID_17206480,Human_RBP_ID_18486108,Human_RBP_ID_19070941 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 73584 RMVar_ID_73584 Human_SNP_ID_595652878 m1A Human chr16 + 14912263 14912263 14912263 TGCGGGGTACCCGGAGAGGTGGGGATGGCTGTAGGGGGCTGCAGGGAAGAGTTCCAGGAGGTGTC TGCGGGGTACCCGGAGAGGTGGGGATGGCTGTGGGGGGCTGCAGGGAAGAGTTCCAGGAGGTGTC A G AC138932.1 Ensembl:ENSG00000183458 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:14912120..14912296 26863196 MeRIP-seq:(Medium) rs1483846446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5669,Human_RBP_ID_234370,Human_RBP_ID_762357,Human_RBP_ID_815772,Human_RBP_ID_3502547,Human_RBP_ID_5088010,Human_RBP_ID_5183196,Human_RBP_ID_5317424,Human_RBP_ID_5357648,Human_RBP_ID_5572718,Human_RBP_ID_8184368,Human_RBP_ID_8231241,Human_RBP_ID_8726145,Human_RBP_ID_8812571,Human_RBP_ID_9421371,Human_RBP_ID_10483276,Human_RBP_ID_12869505,Human_RBP_ID_17125970,Human_RBP_ID_17188989,Human_RBP_ID_17206560,Human_RBP_ID_17257398,Human_RBP_ID_17488729,Human_RBP_ID_18486178,Human_RBP_ID_18926672,Human_RBP_ID_18938806,Human_RBP_ID_21959874,Human_RBP_ID_22523702,Human_RBP_ID_22582055,Human_RBP_ID_26780216 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 73585 RMVar_ID_73585 Human_SNP_ID_595654667 m1A Human chr16 - 14918680 14918671 14918681 TGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCAGGGGGCCGGAGCAGAGGGACAGGCAGGCGAAG TGGGGCTCCTACAGGTGGGGGCAGGAGGCGG__________GAGCAGAGGGACAGGCAGGCGAAG CCGGCCCCCTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14918630..14918781 32194978 MeRIP-seq:(Medium) rs1361371648 Functional Loss DEL dbSNP153 32..41 33 - - - 73586 RMVar_ID_73586 Human_SNP_ID_595654674 m1A Human chr16 - 14918680 14918680 14918680 TGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCAGGGGGCCGGAGCAGAGGGACAGGCAGGCGAAG TGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCGGGGGGCCGGAGCAGAGGGACAGGCAGGCGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14918630..14918781 32194978 MeRIP-seq:(Medium) rs1487227664 Functional Loss SNV dbSNP153 33..33 33 - - - 73587 RMVar_ID_73587 Human_SNP_ID_595654675 m1A Human chr16 - 14918680 14918680 14918680 TGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCAGGGGGCCGGAGCAGAGGGACAGGCAGGCGAAG TGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCCGGGGGCCGGAGCAGAGGGACAGGCAGGCGAAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14918630..14918781 32194978 MeRIP-seq:(Medium) rs1487227664 Functional Loss SNV dbSNP153 33..33 33 - - - 73588 RMVar_ID_73588 Human_SNP_ID_595654681 m1A Human chr16 - 14918687 14918687 14918687 AGGAGGGTGGGGCTCCTACAGGTGGGGGCAGGAGGCGGCAGGGGGCCGGAGCAGAGGGACAGGCA AGGAGGGTGGGGCTCCTACAGGTGGGGGCAGGGGGCGGCAGGGGGCCGGAGCAGAGGGACAGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:14918638..14918855 26863196 MeRIP-seq:(Medium) rs1170426313 Functional Loss SNV dbSNP153 33..33 33 - - - 73589 RMVar_ID_73589 Human_SNP_ID_595655025 m1A Human chr16 - 14919992 14919992 14919992 CACCCGGTGGGCCCGAGCCGGACGCAGTGCTCAGCTGTGGCTGGGTGTGGCTCCCCGGGCAGCCA CACCCGGTGGGCCCGAGCCGGACGCAGTGCTCGGCTGTGGCTGGGTGTGGCTCCCCGGGCAGCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14919930..14920031 32194978 MeRIP-seq:(Medium) rs62038504 Functional Loss SNV dbSNP153 33..33 33 - - - 73590 RMVar_ID_73590 Human_SNP_ID_595655026 m1A Human chr16 - 14919992 14919992 14919992 CACCCGGTGGGCCCGAGCCGGACGCAGTGCTCAGCTGTGGCTGGGTGTGGCTCCCCGGGCAGCCA CACCCGGTGGGCCCGAGCCGGACGCAGTGCTCCGCTGTGGCTGGGTGTGGCTCCCCGGGCAGCCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14919930..14920031 32194978 MeRIP-seq:(Medium) rs62038504 Functional Loss SNV dbSNP153 33..33 33 - - - 73591 RMVar_ID_73591 Human_SNP_ID_595656259 m1A Human chr16 - 14923700 14923700 14923700 GAAGGTCAGGGACTGCTTGTCGTTGATGGTCCACCAGAAGACCATGTCCGAGCCGGCCTCCACCA GAAGGTCAGGGACTGCTTGTCGTTGATGGTCCCCCAGAAGACCATGTCCGAGCCGGCCTCCACCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14922752..14923750 32194978 MeRIP-seq:(Medium) rs1199584617 Functional Loss SNV dbSNP153 33..33 33 - - - 73592 RMVar_ID_73592 Human_SNP_ID_595659937 m1A Human chr16 - 14933181 14933174 14933183 AGGAGAACGCAGCAGGTGGCCCTCTGGATGTGAGTGAAATAGCTACGAGGCGGCCGGTCCCATAT AGGAGAACGCAGCAGGTGGCCCTCTGGATGCGAGTGAAACAGCTACGAGGCGGCCGGTCCCATAT ATTTCACTCA GTTTCACTCG - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14933111..14933211 32194978 MeRIP-seq:(Medium) rs71248053 Functional Loss MNV dbSNP153 31..40 33 - - - 73593 RMVar_ID_73593 Human_SNP_ID_595659941 m1A Human chr16 - 14933181 14933181 14933181 AGGAGAACGCAGCAGGTGGCCCTCTGGATGTGAGTGAAATAGCTACGAGGCGGCCGGTCCCATAT AGGAGAACGCAGCAGGTGGCCCTCTGGATGTGGGTGAAATAGCTACGAGGCGGCCGGTCCCATAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:14933111..14933211 32194978 MeRIP-seq:(Medium) rs1175699132 Functional Loss SNV dbSNP153 33..33 33 - - - 73594 RMVar_ID_73594 Human_SNP_ID_595680738 m1A Human chr16 + 14998388 14998388 14998388 AATGGAAAGAAGCTCATATCCGGAGATATTCCAGGCCCACTCCAGGGCAGGTAGGTGGCACTGAG AATGGAAAGAAGCTCATATCCGGAGATATTCCCGGCCCACTCCAGGGCAGGTAGGTGGCACTGAG A C PDXDC1 Ensembl:ENSG00000179889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:14998288..14998400 26863196 MeRIP-seq:(Medium) rs146743710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199712,Human_RBP_ID_234203,Human_RBP_ID_817528,Human_RBP_ID_891528,Human_RBP_ID_3947296,Human_RBP_ID_9372325,Human_RBP_ID_17872046,Human_RBP_ID_18163505,Human_RBP_ID_18411661,Human_RBP_ID_18985500,Human_RBP_ID_22497177,Human_RBP_ID_22944398,Human_RBP_ID_24544489,Human_RBP_ID_26328682,Human_RBP_ID_27810904 Human_Splice_Rec_1681110,Human_Splice_Rec_1681111,Human_Splice_Rec_1681156,Human_Splice_Rec_1681157,Human_Splice_Rec_1681166,Human_Splice_Rec_1681167,Human_Splice_Rec_1681176,Human_Splice_Rec_1681177,Human_Splice_Rec_1681208,Human_Splice_Rec_1681209,Human_Splice_Rec_1681252,Human_Splice_Rec_1681256,Human_Splice_Rec_1681257,Human_Splice_Rec_1681282,Human_Splice_Rec_1681283,Human_Splice_Rec_1681298,Human_Splice_Rec_1681299,Human_Splice_Rec_1681340,Human_Splice_Rec_1681341,Human_Splice_Rec_1681382,Human_Splice_Rec_1681383,Human_Splice_Rec_1681424,Human_Splice_Rec_1681425,Human_Splice_Rec_1681436,Human_Splice_Rec_1681437,Human_Splice_Rec_1681460,Human_Splice_Rec_1681461,Human_Splice_Rec_1681476,Human_Splice_Rec_1681477 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_176497,RMVar_hsa_circ_104826,RMVar_hsa_circ_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_29630,RMVar_hsa_circ_346735,RMVar_hsa_circ_273763,RMVar_hsa_circ_176499,RMVar_hsa_circ_176500 73595 RMVar_ID_73595 Human_SNP_ID_560927971 m1A Human chr14 - 75063959 75063957 75063960 CGGAGTGATCCTGGCAGCCGGTGGGGAAGACAAGGAGGGTGAGCCGCCAGGGGCCCCCAGGGTGT CGGAGTGATCCTGGCAGCCGGTGGGGAAGAC___GAGGGTGAGCCGCCAGGGGCCCCCAGGGTGT CCTT C ACYP1 Ensembl:ENSG00000119640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75063482..75063992 26863196 MeRIP-seq:(Medium) rs1226170021 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_231466,Human_RBP_ID_4308428,Human_RBP_ID_18418164,Human_RBP_ID_18980862,Human_RBP_ID_27837241 Human_Splice_Rec_1537011,Human_Splice_Rec_1537017,Human_Splice_Rec_1537025,Human_Splice_Rec_1537031 73596 RMVar_ID_73596 Human_SNP_ID_560927973 m1A Human chr14 - 75063959 75063959 75063959 CGGAGTGATCCTGGCAGCCGGTGGGGAAGACAAGGAGGGTGAGCCGCCAGGGGCCCCCAGGGTGT CGGAGTGATCCTGGCAGCCGGTGGGGAAGACAGGGAGGGTGAGCCGCCAGGGGCCCCCAGGGTGT T C ACYP1 Ensembl:ENSG00000119640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75063482..75063992 26863196 MeRIP-seq:(Medium) rs966104216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231466,Human_RBP_ID_4308428,Human_RBP_ID_18418164,Human_RBP_ID_18980862,Human_RBP_ID_27837241 Human_Splice_Rec_1537011,Human_Splice_Rec_1537017,Human_Splice_Rec_1537025,Human_Splice_Rec_1537031 73597 RMVar_ID_73597 Human_SNP_ID_560932739 m1A Human chr14 - 75084097 75084097 75084097 TGGAGTGGGCTGGAATCAGGTGTGGCCCGCCCAGTGTCCTCTGCAGAGTGGTGAAGTAGTCTGGC TGGAGTGGGCTGGAATCAGGTGTGGCCCGCCCGGTGTCCTCTGCAGAGTGGTGAAGTAGTCTGGC T C NEK9 Ensembl:ENSG00000119638 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75084050..75084150 26863196 MeRIP-seq:(Medium) rs1383576855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230824,Human_RBP_ID_451950,Human_RBP_ID_5522839,Human_RBP_ID_6385565,Human_RBP_ID_18161447 Human_miRNA_ID_1959297,Human_miRNA_ID_2273256 RMVar_hsa_circ_87237,RMVar_hsa_circ_167980 73598 RMVar_ID_73598 Human_SNP_ID_560932748 m1A Human chr14 - 75084126 75084126 75084126 TCTGGGTGGGAGAGGGAGAAGTGTAAAGTTGGAGTGGGCTGGAATCAGGTGTGGCCCGCCCAGTG TCTGGGTGGGAGAGGGAGAAGTGTAAAGTTGGGGTGGGCTGGAATCAGGTGTGGCCCGCCCAGTG T C NEK9 Ensembl:ENSG00000119638 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75084076..75084165 26863196 MeRIP-seq:(Medium) rs537371099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451950,Human_RBP_ID_5522840,Human_RBP_ID_18161447 Human_miRNA_ID_2974273,Human_miRNA_ID_3007462 RMVar_hsa_circ_87237,RMVar_hsa_circ_167980 73599 RMVar_ID_73599 Human_SNP_ID_560932854 m1A Human chr14 + 75084595 75084595 75084595 ACTAGAGGCTGGGTCTACAGGAGTCTGTTCCCAGGAGGCACCAGGAATCTGAATCTAAGTCAGGC ACTAGAGGCTGGGTCTACAGGAGTCTGTTCCCGGGAGGCACCAGGAATCTGAATCTAAGTCAGGC A G ZC2HC1C Ensembl:ENSG00000119703 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:75084545..75084918 32194978 MeRIP-seq:(Medium) rs916880902 Functional Loss SNV dbSNP153 33..33 33 - - - 73600 RMVar_ID_73600 Human_SNP_ID_560942280 m1A Human chr14 - 75124174 75124174 75124174 GTGGAAGGAAGTCGATTTGACCCGGCTGTCTGAGAAGGAACGTCGTGATGCCTTGAATGAGATTG GTGGAAGGAAGTCGATTTGACCCGGCTGTCTGCGAAGGAACGTCGTGATGCCTTGAATGAGATTG T G NEK9 Ensembl:ENSG00000119638 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:75124124..75127003 32194978 MeRIP-seq:(Medium) rs770147838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1499624,Human_RBP_ID_5563497,Human_RBP_ID_8410390,Human_RBP_ID_12424252,Human_RBP_ID_23636929,Human_RBP_ID_26326286 Human_Splice_Rec_1537088,Human_Splice_Rec_1537168,Human_Splice_Rec_1537214,Human_Splice_Rec_1537226,Human_Splice_Rec_1537234 RMVar_hsa_circ_337374,RMVar_hsa_circ_373485,RMVar_hsa_circ_106406,RMVar_hsa_circ_167988,RMVar_hsa_circ_125683,RMVar_hsa_circ_167987,RMVar_hsa_circ_299039,RMVar_hsa_circ_167989,RMVar_hsa_circ_309894,RMVar_hsa_circ_167996,RMVar_hsa_circ_292386,RMVar_hsa_circ_168002,RMVar_hsa_circ_353739,RMVar_hsa_circ_373442,RMVar_hsa_circ_168006,RMVar_hsa_circ_291746,RMVar_hsa_circ_344495,RMVar_hsa_circ_309996,RMVar_hsa_circ_168007,RMVar_hsa_circ_117853,RMVar_hsa_circ_334276,RMVar_hsa_circ_291648,RMVar_hsa_circ_168014,RMVar_hsa_circ_168016,RMVar_hsa_circ_288968,RMVar_hsa_circ_168022,RMVar_hsa_circ_168018,RMVar_hsa_circ_168021,RMVar_hsa_circ_289113,RMVar_hsa_circ_284580,RMVar_hsa_circ_168023,RMVar_hsa_circ_273389 73601 RMVar_ID_73601 Human_SNP_ID_560943012 m1A Human chr14 - 75126921 75126921 75126921 CAGGCTGGTCCCCAAGGCCCGCGGCCGCCGCCATGTCGGTGCTGGGCGAGTACGAGCGACACTGC CAGGCTGGTCCCCAAGGCCCGCGGCCGCCGCCGTGTCGGTGCTGGGCGAGTACGAGCGACACTGC T C NEK9 Ensembl:ENSG00000119638 Protein coding start codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:75126903..75127003 32194978 MeRIP-seq:(Medium) rs1002313285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231141,Human_RBP_ID_757063,Human_RBP_ID_4308013,Human_RBP_ID_9370315 Human_Splice_Rec_1537213 RMVar_hsa_circ_167988,RMVar_hsa_circ_125683,RMVar_hsa_circ_117853,RMVar_hsa_circ_168016 73602 RMVar_ID_73602 Human_SNP_ID_560943057 m1A Human chr14 + 75126997 75126997 75126997 AGGCCCTGGCCGCGCTGCGTCCCGCTCGCTTCAGATGCCGGCCCGCGGATCCGTCAGCCCAGCAA AGGCCCTGGCCGCGCTGCGTCCCGCTCGCTTCGGATGCCGGCCCGCGGATCCGTCAGCCCAGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:75126726..75127075 26863196 MeRIP-seq:(Medium) rs905266613 Functional Loss SNV dbSNP153 33..33 33 - - - 73603 RMVar_ID_73603 Human_SNP_ID_560943059 m1A Human chr14 + 75126999 75126999 75126999 GCCCTGGCCGCGCTGCGTCCCGCTCGCTTCAGATGCCGGCCCGCGGATCCGTCAGCCCAGCAACC GCCCTGGCCGCGCTGCGTCCCGCTCGCTTCAGCTGCCGGCCCGCGGATCCGTCAGCCCAGCAACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:75126673..75127050;chr14:75126751..75127075 26863196 MeRIP-seq:(Medium) rs1002261145 Functional Loss SNV dbSNP153 33..33 33 - - - 73604 RMVar_ID_73604 Human_SNP_ID_560954820 m1A Human chr14 - 75176476 75176476 75176476 CGGCCCCAGATTGGTCCTTGCCATCTCCTTCCATCTGCCCATTAACTCTCGCAAGTGCCTCCGTG CGGCCCCAGATTGGTCCTTGCCATCTCCTTCCGTCTGCCCATTAACTCTCGCAAGTGCCTCCGTG T C TMED10 Ensembl:ENSG00000170348 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:75176426..75176625 26863196 MeRIP-seq:(Medium) rs753647635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452123,Human_RBP_ID_757358,Human_RBP_ID_813066,Human_RBP_ID_883993,Human_RBP_ID_1499707,Human_RBP_ID_2426985,Human_RBP_ID_4308014,Human_RBP_ID_5418298,Human_RBP_ID_5439289,Human_RBP_ID_5463559,Human_RBP_ID_8410443,Human_RBP_ID_18656927,Human_RBP_ID_22045080,Human_RBP_ID_22438792,Human_RBP_ID_24410721,Human_RBP_ID_24472497,Human_RBP_ID_26808134,Human_RBP_ID_27432938 Human_miRNA_ID_2619236 RMVar_hsa_circ_119536,RMVar_hsa_circ_168025 73605 RMVar_ID_73605 Human_SNP_ID_560954851 m1A Human chr14 + 75176565 75176565 75176565 AACGGAAAAGGGCCGCGCCGGGCTGGTGGGCCAGACAAACCAGACATGGTGCTGGAGACTCGTTC AACGGAAAAGGGCCGCGCCGGGCTGGTGGGCCTGACAAACCAGACATGGTGCTGGAGACTCGTTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75176320..75176625 26863196 MeRIP-seq:(Medium) rs766167224 Functional Loss SNV dbSNP153 33..33 33 - - - 73606 RMVar_ID_73606 Human_SNP_ID_560954856 m1A Human chr14 + 75176574 75176574 75176574 GGGCCGCGCCGGGCTGGTGGGCCAGACAAACCAGACATGGTGCTGGAGACTCGTTCACCACCGAA GGGCCGCGCCGGGCTGGTGGGCCAGACAAACCCGACATGGTGCTGGAGACTCGTTCACCACCGAA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:75176451..75176625;chr14:75176476..75176625;chr14:75176423..75176625 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1201412551 Functional Loss SNV dbSNP153 33..33 33 - - - 73607 RMVar_ID_73607 Human_SNP_ID_560954857 m1A Human chr14 + 75176574 75176574 75176574 GGGCCGCGCCGGGCTGGTGGGCCAGACAAACCAGACATGGTGCTGGAGACTCGTTCACCACCGAA GGGCCGCGCCGGGCTGGTGGGCCAGACAAACCGGACATGGTGCTGGAGACTCGTTCACCACCGAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:75176451..75176625;chr14:75176476..75176625;chr14:75176423..75176625 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1201412551 Functional Loss SNV dbSNP153 33..33 33 - - - 73608 RMVar_ID_73608 Human_SNP_ID_560974687 m1A Human chr14 + 75258821 75258821 75258821 AGTGGTCTCGGTTTGGCCCTCAGTCTGGAGTCACAGTCTGGATTCACAGGCAGCGCAGAGAGATG AGTGGTCTCGGTTTGGCCCTCAGTCTGGAGTCTCAGTCTGGATTCACAGGCAGCGCAGAGAGATG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75258771..75258839 26863196 MeRIP-seq:(Medium) rs1309308524 Functional Loss SNV dbSNP153 33..33 33 - - - 73609 RMVar_ID_73609 Human_SNP_ID_560979392 m1A Human chr14 + 75278910 75278910 75278910 CGGCGCAGCGAACGAGCAGTGACCGTGCTCCTACCCAGCTCTGCTCCACAGCGCCCACCTGTCTC CGGCGCAGCGAACGAGCAGTGACCGTGCTCCTCCCCAGCTCTGCTCCACAGCGCCCACCTGTCTC A C FOS Ensembl:ENSG00000170345 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75278860..75279060 26863196 MeRIP-seq:(Medium) rs1423582911 Functional Loss SNV dbSNP153 33..33 33 - - - 73610 RMVar_ID_73610 Human_SNP_ID_560979451 m1A Human chr14 + 75279074 75279042 75279075 GTCCCCGGCCGGGGATAGCCTCTCTTACTACCACTCACCCGCAGACTCCTTCTCCAGCATGGGCT G_________________________________TCACCCGCAGACTCCTTCTCCAGCATGGGCT GTCCCCGGCCGGGGATAGCCTCTCTTACTACCAC G FOS Ensembl:ENSG00000170345 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:75279051..75279075 26863196 MeRIP-seq:(Medium) rs1566699946 Functional Loss DEL dbSNP153 2..34 33 - - - Human_RBP_ID_27432941 Human_Splice_Rec_1537293,Human_Splice_Rec_1537295,Human_Splice_Rec_1537299,Human_Splice_Rec_1537303,Human_Splice_Rec_1537309 73611 RMVar_ID_73611 Human_SNP_ID_560979468 m1A Human chr14 - 75279070 75279070 75279070 CATGCTGGAGAAGGAGTCTGCGGGTGAGTGGTAGTAAGAGAGGCTATCCCCGGCCGGGGACGCGC CATGCTGGAGAAGGAGTCTGCGGGTGAGTGGTGGTAAGAGAGGCTATCCCCGGCCGGGGACGCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:75279022..75279123 32194978 MeRIP-seq:(Medium) rs1360829507 Functional Loss SNV dbSNP153 33..33 33 - - - 73612 RMVar_ID_73612 Human_SNP_ID_560980110 m1A Human chr14 - 75281173 75281171 75281174 ACTGTGCAGAGGCTCCCAGTCTGCTGCATAGAAGGACCCAGATAGGTCCATGTCTGGCACGGAGC ACTGTGCAGAGGCTCCCAGTCTGCTGCATAG___GACCCAGATAGGTCCATGTCTGGCACGGAGC CCTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:75281026..75281225 26863196 MeRIP-seq:(Medium) rs1371451462 Functional Loss DEL dbSNP153 32..34 33 - - - 73613 RMVar_ID_73613 Human_SNP_ID_561014655 m1A Human chr14 + 75428094 75428076 75428094 CGACGGGGGGCGCTGGCGGCGGCGGACGCTGCAGCGGCGGCGGGGCTGGCGCCGCGGCGGCTCCC CGACGGGGGGCGCTG__________________GCGGCGGCGGGGCTGGCGCCGCGGCGGCTCCC GGCGGCGGCGGACGCTGCA G JDP2 Ensembl:ENSG00000140044 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75428050..75428287 26863196 MeRIP-seq:(Medium) rs996936040 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_3468722,Human_RBP_ID_4308936 73614 RMVar_ID_73614 Human_SNP_ID_561014663 m1A Human chr14 + 75428094 75428094 75428094 CGACGGGGGGCGCTGGCGGCGGCGGACGCTGCAGCGGCGGCGGGGCTGGCGCCGCGGCGGCTCCC CGACGGGGGGCGCTGGCGGCGGCGGACGCTGCGGCGGCGGCGGGGCTGGCGCCGCGGCGGCTCCC A G JDP2 Ensembl:ENSG00000140044 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75428050..75428287 26863196 MeRIP-seq:(Medium) rs1408474788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3468722,Human_RBP_ID_4308936 73615 RMVar_ID_73615 Human_SNP_ID_561014691 m1A Human chr14 + 75428203 75428203 75428203 CGGCAGCGGCGCGGAGCGGGCACGGCGCCTGCAGCCGGGCCCCGGCCCCGGGGGCGCCGCCTCCC CGGCAGCGGCGCGGAGCGGGCACGGCGCCTGCTGCCGGGCCCCGGCCCCGGGGGCGCCGCCTCCC A T JDP2 Ensembl:ENSG00000140044 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:75428110..75428365 26863410 MeRIP-seq:(Medium) rs1388222137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308936 Human_Splice_Rec_1537347,Human_Splice_Rec_1537353,Human_Splice_Rec_1537359,Human_Splice_Rec_1537363 73616 RMVar_ID_73616 Human_SNP_ID_561014836 m1A Human chr14 - 75428608 75428608 75428608 GCCCATCTCCGCGGGCACTTTTCTCCCCACTCACCCCGCCTTCCCCGCCGCCCGAGGAGAGCACC GCCCATCTCCGCGGGCACTTTTCTCCCCACTCCCCCCGCCTTCCCCGCCGCCCGAGGAGAGCACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:75428600..75428864;chr14:75428603..75428810 26863196 MeRIP-seq:(Medium) rs1566731479 Functional Loss SNV dbSNP153 33..33 33 - - - 73617 RMVar_ID_73617 Human_SNP_ID_561017000 m1A Human chr14 - 75437878 75437878 75437878 GTGGCAGGCCAGCCTGGAGTGGGCAGGAAAAGAGCAGGACAGTCAGCCAGGTTGGGGGCTCCAGG GTGGCAGGCCAGCCTGGAGTGGGCAGGAAAAGGGCAGGACAGTCAGCCAGGTTGGGGGCTCCAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75437876..75437975 26863196 MeRIP-seq:(Medium) rs989996822 Functional Loss SNV dbSNP153 33..33 33 - - - 73618 RMVar_ID_73618 Human_SNP_ID_561017094 m1A Human chr14 + 75438105 75438105 75438105 CTTCCTGGAGGTGAAACTGGGCAAGAGGCCCCAGCCCGTGAAAAGTGAGGTGAGCGAGCCTTTTA CTTCCTGGAGGTGAAACTGGGCAAGAGGCCCCGGCCCGTGAAAAGTGAGGTGAGCGAGCCTTTTA A G JDP2 Ensembl:ENSG00000140044 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75438056..75438162 26863196 MeRIP-seq:(Medium) rs760581429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1537339,Human_Splice_Rec_1537345,Human_Splice_Rec_1537349,Human_Splice_Rec_1537355,Human_Splice_Rec_1537361,Human_Splice_Rec_1537365,Human_Splice_Rec_1537371,Human_Splice_Rec_1537377 Human_miRNA_ID_1356640,Human_miRNA_ID_2685159 RMVar_hsa_circ_26638,RMVar_hsa_circ_82507,RMVar_hsa_circ_367402,RMVar_hsa_circ_168027 73619 RMVar_ID_73619 Human_SNP_ID_561018753 m1A Human chr14 + 75445324 75445324 75445324 AGTGAGGGCCTGGGCCTCCTCTGGGTTTAGCCACCCTTCCAGGTTGTGTACAACCTGCCATATGC AGTGAGGGCCTGGGCCTCCTCTGGGTTTAGCCCCCCTTCCAGGTTGTGTACAACCTGCCATATGC A C JDP2 Ensembl:ENSG00000140044 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:75445318..75469423 32194978 MeRIP-seq:(Medium) rs1379162922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82507,RMVar_hsa_circ_367402,RMVar_hsa_circ_168027 73620 RMVar_ID_73620 Human_SNP_ID_561020137 m1A Human chr14 - 75451580 75451580 75451580 CCAGGTCCCATCCTTGGCCTGCTACTCTCCTCACTCGATACGCACGGCCTGTGGATCTCCGTTTG CCAGGTCCCATCCTTGGCCTGCTACTCTCCTCTCTCGATACGCACGGCCTGTGGATCTCCGTTTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75451578..75451674 26863196 MeRIP-seq:(Medium) rs983100233 Functional Loss SNV dbSNP153 33..33 33 - - - 73621 RMVar_ID_73621 Human_SNP_ID_561020138 m1A Human chr14 - 75451580 75451580 75451580 CCAGGTCCCATCCTTGGCCTGCTACTCTCCTCACTCGATACGCACGGCCTGTGGATCTCCGTTTG CCAGGTCCCATCCTTGGCCTGCTACTCTCCTCGCTCGATACGCACGGCCTGTGGATCTCCGTTTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75451578..75451674 26863196 MeRIP-seq:(Medium) rs983100233 Functional Loss SNV dbSNP153 33..33 33 - - - 73622 RMVar_ID_73622 Human_SNP_ID_561024345 m1A Human chr14 - 75469920 75469920 75469920 TTCGCATCAGGGCGAGGGGCAGGGCTGGGGGCAGGTGGGTTGCAGTTTCATTCTGAGTTCCATCC TTCGCATCAGGGCGAGGGGCAGGGCTGGGGGCGGGTGGGTTGCAGTTTCATTCTGAGTTCCATCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:75469874..75470090 26863196 MeRIP-seq:(Medium) rs934015841 Functional Loss SNV dbSNP153 33..33 33 - - - 73623 RMVar_ID_73623 Human_SNP_ID_561051822 m1A Human chr14 - 75578752 75578752 75578752 TTGCTTGGGGCTCTCTGTTGCCACCCGCGGCGATCGCTGTCCCAAGGCCGGCCGCACACGCCGCA TTGCTTGGGGCTCTCTGTTGCCACCCGCGGCGTTCGCTGTCCCAAGGCCGGCCGCACACGCCGCA T A AC007182.1 Ensembl:ENSG00000224721 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75578606..75578755 26863196 MeRIP-seq:(Medium) rs1266175066 Functional Loss SNV dbSNP153 33..33 33 - - - 73624 RMVar_ID_73624 Human_SNP_ID_561068552 m1A Human chr14 - 75651126 75651126 75651126 ACCCAGAGCAGCTGTGACCAAGGGCTGCCTCAAGGGGTTGTCCACGCAGGTTGGGCTCCTCTCTG ACCCAGAGCAGCTGTGACCAAGGGCTGCCTCACGGGGTTGTCCACGCAGGTTGGGCTCCTCTCTG T G ERG28 Ensembl:ENSG00000133935 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:75650901..75651231 32194978 MeRIP-seq:(Medium) rs1209876784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231204,Human_RBP_ID_452160,Human_RBP_ID_1276713,Human_RBP_ID_5112425,Human_RBP_ID_5140893,Human_RBP_ID_12424799,Human_RBP_ID_17363372,Human_RBP_ID_23208579,Human_RBP_ID_26808136,Human_RBP_ID_27228954 RMVar_hsa_circ_85150,RMVar_hsa_circ_168038 73625 RMVar_ID_73625 Human_SNP_ID_561070674 m1A Human chr14 + 75660825 75660825 75660825 GCACAGCAGTGGCAGCAGCAGCCGCTGCCGCAAACAAGCTCCCCCAGGACAGCTCCAGCCCGGAG GCACAGCAGTGGCAGCAGCAGCCGCTGCCGCAGACAAGCTCCCCCAGGACAGCTCCAGCCCGGAG A G TTLL5,FLVCR2 Ensembl:ENSG00000119685,Ensembl:ENSG00000119686 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75660684..75660834 26863196 MeRIP-seq:(Medium) rs372565121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168037 73626 RMVar_ID_73626 Human_SNP_ID_561070853 m1A Human chr14 - 75661303 75661303 75661303 CCTACCTCCCTCCTCCTTCCCCAGGAAGGCTCAGGGCAGCCGCCGACGGCTGCTTCCCCGGTTAC CCTACCTCCCTCCTCCTTCCCCAGGAAGGCTCTGGGCAGCCGCCGACGGCTGCTTCCCCGGTTAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75661257..75661359 26863196 MeRIP-seq:(Medium) rs1226532399 Functional Loss SNV dbSNP153 33..33 33 - - - 73627 RMVar_ID_73627 Human_SNP_ID_561078359 m1A Human chr14 + 75692915 75692915 75692915 CAGTTGTAAGAGCAGGTTTGAGTTCTGGCCAGAGATGTAGATTCTGGAAGCTGCAGTATGGAGAT CAGTTGTAAGAGCAGGTTTGAGTTCTGGCCAGCGATGTAGATTCTGGAAGCTGCAGTATGGAGAT A C TTLL5 Ensembl:ENSG00000119685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75692908..75693158 26863196 MeRIP-seq:(Medium) rs1026732315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12424991 RMVar_hsa_circ_106987,RMVar_hsa_circ_118612,RMVar_hsa_circ_14753,RMVar_hsa_circ_265208,RMVar_hsa_circ_168039,RMVar_hsa_circ_124402,RMVar_hsa_circ_48609,RMVar_hsa_circ_168042,RMVar_hsa_circ_97030,RMVar_hsa_circ_168043,RMVar_hsa_circ_93867,RMVar_hsa_circ_41958,RMVar_hsa_circ_52637,RMVar_hsa_circ_104325,RMVar_hsa_circ_168044,RMVar_hsa_circ_168045,RMVar_hsa_circ_168046 73628 RMVar_ID_73628 Human_SNP_ID_561078360 m1A Human chr14 + 75692915 75692915 75692915 CAGTTGTAAGAGCAGGTTTGAGTTCTGGCCAGAGATGTAGATTCTGGAAGCTGCAGTATGGAGAT CAGTTGTAAGAGCAGGTTTGAGTTCTGGCCAGGGATGTAGATTCTGGAAGCTGCAGTATGGAGAT A G TTLL5 Ensembl:ENSG00000119685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75692908..75693158 26863196 MeRIP-seq:(Medium) rs1026732315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12424991 RMVar_hsa_circ_106987,RMVar_hsa_circ_118612,RMVar_hsa_circ_14753,RMVar_hsa_circ_265208,RMVar_hsa_circ_168039,RMVar_hsa_circ_124402,RMVar_hsa_circ_48609,RMVar_hsa_circ_168042,RMVar_hsa_circ_97030,RMVar_hsa_circ_168043,RMVar_hsa_circ_93867,RMVar_hsa_circ_41958,RMVar_hsa_circ_52637,RMVar_hsa_circ_104325,RMVar_hsa_circ_168044,RMVar_hsa_circ_168045,RMVar_hsa_circ_168046 73629 RMVar_ID_73629 Human_SNP_ID_561083808 m1A Human chr14 + 75716031 75716031 75716031 TAATTCATTGTTCTTTGAGGGGAGAGGATGACAGGAGGGATGTCACCTTGAGGTAATGTCTGGCT TAATTCATTGTTCTTTGAGGGGAGAGGATGACGGGAGGGATGTCACCTTGAGGTAATGTCTGGCT A G TTLL5 Ensembl:ENSG00000119685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75716029..75716112 26863196 MeRIP-seq:(Medium) rs957991720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106987,RMVar_hsa_circ_118612,RMVar_hsa_circ_14753,RMVar_hsa_circ_265208,RMVar_hsa_circ_168039,RMVar_hsa_circ_124402,RMVar_hsa_circ_48609,RMVar_hsa_circ_168042,RMVar_hsa_circ_97030,RMVar_hsa_circ_168043,RMVar_hsa_circ_45816,RMVar_hsa_circ_33875,RMVar_hsa_circ_93867,RMVar_hsa_circ_104325,RMVar_hsa_circ_168044,RMVar_hsa_circ_168045,RMVar_hsa_circ_168046,RMVar_hsa_circ_345221,RMVar_hsa_circ_113136,RMVar_hsa_circ_277206,RMVar_hsa_circ_332583,RMVar_hsa_circ_168047,RMVar_hsa_circ_309935,RMVar_hsa_circ_279271,RMVar_hsa_circ_88226,RMVar_hsa_circ_118188,RMVar_hsa_circ_50529,RMVar_hsa_circ_168049,RMVar_hsa_circ_168051,RMVar_hsa_circ_16731,RMVar_hsa_circ_168052,RMVar_hsa_circ_168050,RMVar_hsa_circ_168048 73630 RMVar_ID_73630 Human_SNP_ID_561095873 m1A Human chr14 + 75768589 75768589 75768589 GATAAGAGGATTAGAAATGCAGAAATGGACATATTGGTAGAGAAGAGTACTAAAGGAAGGTGGGA GATAAGAGGATTAGAAATGCAGAAATGGACATGTTGGTAGAGAAGAGTACTAAAGGAAGGTGGGA A G TTLL5 Ensembl:ENSG00000119685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75768578..75768689 26863196 MeRIP-seq:(Medium) rs970564297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124402,RMVar_hsa_circ_168042,RMVar_hsa_circ_97030,RMVar_hsa_circ_168043,RMVar_hsa_circ_93867,RMVar_hsa_circ_168046,RMVar_hsa_circ_113136,RMVar_hsa_circ_168047,RMVar_hsa_circ_88226,RMVar_hsa_circ_50529,RMVar_hsa_circ_168048,RMVar_hsa_circ_1492,RMVar_hsa_circ_104278,RMVar_hsa_circ_59400,RMVar_hsa_circ_168058,RMVar_hsa_circ_168065,RMVar_hsa_circ_85137,RMVar_hsa_circ_100670,RMVar_hsa_circ_168063,RMVar_hsa_circ_81757,RMVar_hsa_circ_319000,RMVar_hsa_circ_168064,RMVar_hsa_circ_365276,RMVar_hsa_circ_311873,RMVar_hsa_circ_6263,RMVar_hsa_circ_168067,RMVar_hsa_circ_168068,RMVar_hsa_circ_112637,RMVar_hsa_circ_85754,RMVar_hsa_circ_349318,RMVar_hsa_circ_168070,RMVar_hsa_circ_168071,RMVar_hsa_circ_325643,RMVar_hsa_circ_369020,RMVar_hsa_circ_288684,RMVar_hsa_circ_31393,RMVar_hsa_circ_11154,RMVar_hsa_circ_23027,RMVar_hsa_circ_336276,RMVar_hsa_circ_168072,RMVar_hsa_circ_368814,RMVar_hsa_circ_43191,RMVar_hsa_circ_168073 73631 RMVar_ID_73631 Human_SNP_ID_561127786 m1A Human chr14 + 75903271 75903271 75903271 CTGGGAACGGCTTCCTAGAGGAAAAACATCGAAGCTGACACTGGAGTGTGGACGAGTCAGCCAGG CTGGGAACGGCTTCCTAGAGGAAAAACATCGAGGCTGACACTGGAGTGTGGACGAGTCAGCCAGG A G IFT43,TTLL5 Ensembl:ENSG00000119650,Ensembl:ENSG00000119685 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:75903266..75903525 26863196 MeRIP-seq:(Medium) rs1005022184 Functional Loss SNV dbSNP153 33..33 33 - - - 73632 RMVar_ID_73632 Human_SNP_ID_561146836 m1A Human chr14 - 75981847 75981847 75981847 GAGAGAGGCAGAGACAGGGGAAGAGGCGTGCGAGAGAAGGAATAACAGCTTTCCGGAGCAGGCGT GAGAGAGGCAGAGACAGGGGAAGAGGCGTGCGGGAGAAGGAATAACAGCTTTCCGGAGCAGGCGT T C TGFB3 Ensembl:ENSG00000119699 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75981808..75981942 26863196 MeRIP-seq:(Medium) rs1161058142 Functional Loss SNV dbSNP153 33..33 33 - - - 73633 RMVar_ID_73633 Human_SNP_ID_561146848 m1A Human chr14 - 75981896 75981896 75981896 GAGAGAGAGAAAGGGAGGGAAGCAGAGAGTCAAGTCCAAGGGAATGAGCGAGAGAGGCAGAGACA GAGAGAGAGAAAGGGAGGGAAGCAGAGAGTCACGTCCAAGGGAATGAGCGAGAGAGGCAGAGACA T G TGFB3 Ensembl:ENSG00000119699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:75981750..75982049;chr14:75981768..75982091 26863196 MeRIP-seq:(Medium) rs1013195969 Functional Loss SNV dbSNP153 33..33 33 - - - 73634 RMVar_ID_73634 Human_SNP_ID_561146850 m1A Human chr14 - 75981901 75981899 75981901 AGAGGGAGAGAGAGAAAGGGAGGGAAGCAGAGAGTCAAGTCCAAGGGAATGAGCGAGAGAGGCAG AGAGGGAGAGAGAGAAAGGGAGGGAAGCAGAG__TCAAGTCCAAGGGAATGAGCGAGAGAGGCAG ACT A TGFB3 Ensembl:ENSG00000119699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75981763..75982035 26863196 MeRIP-seq:(Medium) rs955256905 Functional Loss DEL dbSNP153 33..34 33 - - - 73635 RMVar_ID_73635 Human_SNP_ID_561147846 m1A Human chr14 - 75985842 75985842 75985842 TCCTGGCCCCCAAGGCCCCCGAATTGGTCCTCACGGAGGTAGCCAAGCTGTAGCGAAGCTCCTCG TCCTGGCCCCCAAGGCCCCCGAATTGGTCCTCTCGGAGGTAGCCAAGCTGTAGCGAAGCTCCTCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr14:75985809..75985896;chr14:75985762..75985863 26863196,32194978 MeRIP-seq:(Medium) rs771473725 Functional Loss SNV dbSNP153 33..33 33 - - - 73636 RMVar_ID_73636 Human_SNP_ID_561148010 m1A Human chr14 - 75986262 75986262 75986262 GTCCCTGCCTGCCTCCCTTCCATGCATAAAACAGTGCGGCTTTTGCAGGAACTTCTGCGACGAGG GTCCCTGCCTGCCTCCCTTCCATGCATAAAACGGTGCGGCTTTTGCAGGAACTTCTGCGACGAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:75986259..76022431 32194978 MeRIP-seq:(Medium) rs896696244 Functional Loss SNV dbSNP153 33..33 33 - - - 73637 RMVar_ID_73637 Human_SNP_ID_561148633 m1A Human chr14 + 75988858 75988858 75988858 ATCTCAGTAGTGGCCCAAATGACATTTGGGTCAGCAGTGCCTTCTGTTTCTCCTTACAGAGGGCC ATCTCAGTAGTGGCCCAAATGACATTTGGGTCGGCAGTGCCTTCTGTTTCTCCTTACAGAGGGCC A G IFT43 Ensembl:ENSG00000119650 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:75988836..75988922 26863410 MeRIP-seq:(Medium) rs760295093 Functional Loss SNV dbSNP153 33..33 33 - - - 73638 RMVar_ID_73638 Human_SNP_ID_561148672 m1A Human chr14 - 75988935 75988935 75988935 AGAGTCAAAGAGGAATTCTTGCCATTGAGGTGATTCTCGGCCTGCGCTGACTCCTGTTGAGCTCG AGAGTCAAAGAGGAATTCTTGCCATTGAGGTGGTTCTCGGCCTGCGCTGACTCCTGTTGAGCTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75988859..75988938 26863196 MeRIP-seq:(Medium) rs370919728 Functional Loss SNV dbSNP153 33..33 33 - - - 73639 RMVar_ID_73639 Human_SNP_ID_561199654 m1A Human chr14 + 76203104 76203104 76203104 CCACTCATGCATCTGCTTATTTTCTGTCTTAAATAGGTGCTGAATGGGGCAGCACCTCCTTCCCC CCACTCATGCATCTGCTTATTTTCTGTCTTAAGTAGGTGCTGAATGGGGCAGCACCTCCTTCCCC A G GPATCH2L Ensembl:ENSG00000089916 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:76203066..76203212 26863196 MeRIP-seq:(Medium) rs971998711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452267,Human_RBP_ID_6387071,Human_RBP_ID_17687661,Human_RBP_ID_17853753 73640 RMVar_ID_73640 Human_SNP_ID_561338858 m1A Human chr14 + 76763116 76763116 76763116 GAGAGAAGGTGGCGCAACGGATCCGTGGGGCCACAGACCTGCCCAAGGTGAGACACACGGGTCAG GAGAGAAGGTGGCGCAACGGATCCGTGGGGCCGCAGACCTGCCCAAGGTGAGACACACGGGTCAG A G VASH1 Ensembl:ENSG00000071246 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:76762833..76769981 32194978 MeRIP-seq:(Medium) rs1172176904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1538273,Human_Splice_Rec_1538285 73641 RMVar_ID_73641 Human_SNP_ID_561343538 m1A Human chr14 + 76780300 76780298 76780300 TGGGGGATGCAAGTGAGAAAGGGATGTGGGGGAGAGTTCAGGATCAGGCTGCTTGAGGAGTAATG TGGGGGATGCAAGTGAGAAAGGGATGTGGGG__GAGTTCAGGATCAGGCTGCTTGAGGAGTAATG GGA G VASH1,AF111169.1 Ensembl:ENSG00000071246,Ensembl:ENSG00000258610 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:76780170..76780522 26863196 MeRIP-seq:(Medium) rs1168552425 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5564638,Human_RBP_ID_6387277,Human_RBP_ID_23637763 RMVar_hsa_circ_168131 73642 RMVar_ID_73642 Human_SNP_ID_561344055 m1A Human chr14 + 76782319 76782319 76782319 TTGGGATGTGATGATAAAGCAAGCCTAGGGCCAGGGTTTGGGGAGCAGAGAGAGCCAAGAAGTTG TTGGGATGTGATGATAAAGCAAGCCTAGGGCCGGGGTTTGGGGAGCAGAGAGAGCCAAGAAGTTG A G VASH1 Ensembl:ENSG00000071246 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:76782220..76782320 32194978 MeRIP-seq:(Medium) rs1283492381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452356,Human_RBP_ID_6387282,Human_RBP_ID_18276320 Human_miRNA_ID_75804,Human_miRNA_ID_78975,Human_miRNA_ID_939212 73643 RMVar_ID_73643 Human_SNP_ID_561344163 m1A Human chr14 + 76782815 76782815 76782815 AGAGAGAAGAAACATGGGTGTGCTTGGCCCACAGGGCCTGGTGGTGATGGACCTCCCCGCTCCCT AGAGAGAAGAAACATGGGTGTGCTTGGCCCACGGGGCCTGGTGGTGATGGACCTCCCCGCTCCCT A G VASH1 Ensembl:ENSG00000071246 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:76782766..76782916 32194978 MeRIP-seq:(Medium) rs1483491979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_864409,Human_miRNA_ID_975636 RMVar_hsa_circ_168133 73644 RMVar_ID_73644 Human_SNP_ID_561351553 m1A Human chr14 - 76812824 76812824 76812824 GGAGCGGAGGCGGGCGCGGGCGGCCGGCCATGATCGCGTCGTGCTTGTGTTACCTGCTGCTGCCG GGAGCGGAGGCGGGCGCGGGCGGCCGGCCATGGTCGCGTCGTGCTTGTGTTACCTGCTGCTGCCG T C ANGEL1 Ensembl:ENSG00000013523 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:76812720..76812893 26863196 MeRIP-seq:(Medium) rs1208101245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758021,Human_RBP_ID_1499880,Human_RBP_ID_4303169,Human_RBP_ID_5353226,Human_RBP_ID_18657238 Human_Splice_Rec_1538319,Human_Splice_Rec_1538355 73645 RMVar_ID_73645 Human_SNP_ID_561351583 m1A Human chr14 - 76812854 76812854 76812854 AGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGCCATGATC AGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGGGCGGAGGCGGGCGCGGGCGGCCGGCCATGATC T C ANGEL1 Ensembl:ENSG00000013523 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:76812694..76812890 26863196 MeRIP-seq:(Medium) rs933291333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758021,Human_RBP_ID_812891,Human_RBP_ID_4308018,Human_RBP_ID_5353226 Human_Splice_Rec_1538319,Human_Splice_Rec_1538355 73646 RMVar_ID_73646 Human_SNP_ID_561351584 m1A Human chr14 - 76812854 76812854 76812854 AGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGCCATGATC AGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGCGCGGAGGCGGGCGCGGGCGGCCGGCCATGATC T G ANGEL1 Ensembl:ENSG00000013523 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:76812694..76812890 26863196 MeRIP-seq:(Medium) rs933291333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758021,Human_RBP_ID_812891,Human_RBP_ID_4308018,Human_RBP_ID_5353226 Human_Splice_Rec_1538319,Human_Splice_Rec_1538355 73647 RMVar_ID_73647 Human_SNP_ID_561351588 m1A Human chr14 - 76812861 76812861 76812861 GGGGCCGAGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGC GGGGCCGAGCTGAGGGAGGACCTGCTGGCTGCGGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGC T C ANGEL1 Ensembl:ENSG00000013523 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:76812703..76812879 26863196 MeRIP-seq:(Medium) rs1266184575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758021,Human_RBP_ID_4308018 Human_Splice_Rec_1538319,Human_Splice_Rec_1538355 73648 RMVar_ID_73648 Human_SNP_ID_561351589 m1A Human chr14 - 76812861 76812861 76812861 GGGGCCGAGCTGAGGGAGGACCTGCTGGCTGCAGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGC GGGGCCGAGCTGAGGGAGGACCTGCTGGCTGCCGTGAGGAGCGGAGGCGGGCGCGGGCGGCCGGC T G ANGEL1 Ensembl:ENSG00000013523 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:76812703..76812879 26863196 MeRIP-seq:(Medium) rs1266184575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758021,Human_RBP_ID_4308018 Human_Splice_Rec_1538319,Human_Splice_Rec_1538355 73649 RMVar_ID_73649 Human_SNP_ID_561406644 m1A Human chr14 - 77025674 77025674 77025674 AAGTGCACCCCCAAAACATTCCGGATTCCCCCATGGCCAACAGCGGACCCCTCTGCTGCACCATT AAGTGCACCCCCAAAACATTCCGGATTCCCCCTTGGCCAACAGCGGACCCCTCTGCTGCACCATT T A IRF2BPL Ensembl:ENSG00000119669 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77025623..77026001 26863196 MeRIP-seq:(Medium) rs746822728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8077774,Human_RBP_ID_8410749,Human_RBP_ID_27229091,Human_RBP_ID_27433029 73650 RMVar_ID_73650 Human_SNP_ID_561407267 m1A Human chr14 + 77026789 77026789 77026789 CCTTCAACTCGCGCTCCTGGTCTGTGCTCGACACCGAGCCGGGCCTCTTACCACCAGCACCCACG CCTTCAACTCGCGCTCCTGGTCTGTGCTCGACTCCGAGCCGGGCCTCTTACCACCAGCACCCACG A T NONHSAG015534.2 RNACentral:URS00009B15C9 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77026745..77026828 26863196 MeRIP-seq:(Medium) rs1188240191 Functional Loss SNV dbSNP153 33..33 33 - - - 73651 RMVar_ID_73651 Human_SNP_ID_561407521 m1A Human chr14 + 77027136 77027133 77027136 CCACGCCGAGACGCCACCGACGCCGCCGCTGAAGAAGAATTGGGGCTCTGACGGTTCAGCTCTGG CCACGCCGAGACGCCACCGACGCCGCCGCT___GAAGAATTGGGGCTCTGACGGTTCAGCTCTGG TGAA T NONHSAG015534.2 RNACentral:URS00009B15C9 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77027085..77027289 26863196 MeRIP-seq:(Medium) rs746345568 Functional Loss DEL dbSNP153 31..33 33 - - - 73652 RMVar_ID_73652 Human_SNP_ID_561408143 m1A Human chr14 + 77027774 77027774 77027774 GCACAGGTAGCAAGATTGTCTCCGGGACGAGGACACCTGCGCCGCCGACATGATGCCTGCCCTGG GCACAGGTAGCAAGATTGTCTCCGGGACGAGGCCACCTGCGCCGCCGACATGATGCCTGCCCTGG A C NONHSAG015534.2 RNACentral:URS00009B15C9 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:77027723..77027790 26863196 MeRIP-seq:(Medium) rs1422747888 Functional Loss SNV dbSNP153 33..33 33 - - - 73653 RMVar_ID_73653 Human_SNP_ID_561408337 m1A Human chr14 - 77028105 77028105 77028105 CGGGCACCCTCGCCCCCTCCCCTCGGGCCGGGAGCTTCCAGCCCAAGTCTGCAGCACCAGGAAGA CGGGCACCCTCGCCCCCTCCCCTCGGGCCGGGTGCTTCCAGCCCAAGTCTGCAGCACCAGGAAGA T A IRF2BPL Ensembl:ENSG00000119669 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:77028055..77028265;chr14:77028062..77028262 26863196 MeRIP-seq:(Medium) rs780880693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_121358,Human_RBP_ID_5177204 73654 RMVar_ID_73654 Human_SNP_ID_561408370 m1A Human chr14 - 77028183 77028183 77028183 AGGAAGAGACAGCCCCTTTCGAGCTTCCACGCACCAGCCACTCCGGGGAGGGGGCCAAGAGGCAA AGGAAGAGACAGCCCCTTTCGAGCTTCCACGCCCCAGCCACTCCGGGGAGGGGGCCAAGAGGCAA T G IRF2BPL Ensembl:ENSG00000119669 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77028067..77028279 26863196 MeRIP-seq:(Medium) rs921659303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_121358,Human_RBP_ID_5236193,Human_RBP_ID_9323823,Human_RBP_ID_22711272 73655 RMVar_ID_73655 Human_SNP_ID_561469216 m1A Human chr14 - 77269794 77269726 77269794 GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGG_________________________________ CTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCCTCTCCCTCT C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77269785..77269915 26863196 MeRIP-seq:(Medium) rs1566637494 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_17067592 73656 RMVar_ID_73656 Human_SNP_ID_561469258 m1A Human chr14 - 77269794 77269787 77269794 GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGG_______GAGGGAGAGAGAGAGAGAGAGAGAGA CTCCCTCT C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77269785..77269915 26863196 MeRIP-seq:(Medium) rs1241663084 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_17067592 73657 RMVar_ID_73657 Human_SNP_ID_561469266 m1A Human chr14 - 77269794 77269791 77269794 GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGG___GGGAGAGGGAGAGAGAGAGAGAGAGAGAGA CTCT C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77269785..77269915 26863196 MeRIP-seq:(Medium) rs1188581530 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_17067592 73658 RMVar_ID_73658 Human_SNP_ID_561469267 m1A Human chr14 - 77269792 77269792 77269792 AGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGAGA AGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGAGAGGGAGAGAGAGAGAGAGAGAGAGAGA T C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:77269784..77269913 26863196 MeRIP-seq:(Medium) rs924471126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17067592 73659 RMVar_ID_73659 Human_SNP_ID_561469271 m1A Human chr14 - 77269794 77269793 77269794 GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGG_GAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA CT C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77269785..77269915 26863196 MeRIP-seq:(Medium) rs1419716838 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17067592 73660 RMVar_ID_73660 Human_SNP_ID_561469272 m1A Human chr14 - 77269794 77269794 77269794 GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA GCAGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGA T C NGB Ensembl:ENSG00000165553 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77269785..77269915 26863196 MeRIP-seq:(Medium) rs200215876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17067592 73661 RMVar_ID_73661 Human_SNP_ID_561470810 m1A Human chr14 - 77275051 77275051 77275051 GGTGGAGGAAGAAGATGTTCGTCAGCCAATTCAACCTCCAGCCAGCTTCTTGAGCCTATTTGGTT GGTGGAGGAAGAAGATGTTCGTCAGCCAATTCGACCTCCAGCCAGCTTCTTGAGCCTATTTGGTT T C POMT2 Ensembl:ENSG00000009830 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11547793 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_337 GWAS_ID_8921,GWAS_ID_8922 73662 RMVar_ID_73662 Human_SNP_ID_561473529 m1A Human chr14 + 77284647 77284647 77284647 GAGGCATAAAGGGAAAGTAGCAGCTTGCTCCAAGCCTGGAGGCTGGGGAGGTGCCCATGGTGCAG GAGGCATAAAGGGAAAGTAGCAGCTTGCTCCAGGCCTGGAGGCTGGGGAGGTGCCCATGGTGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:77284640..77284729 26863196 MeRIP-seq:(Medium) rs894420604 Functional Loss SNV dbSNP153 33..33 33 - - - 73663 RMVar_ID_73663 Human_SNP_ID_561482252 m1A Human chr14 - 77320724 77320724 77320724 TGTGACTCCTTGGCGGGGCGGCTGGTCAGACAAAGTGTGCCTCCGGGCCGGAGGGCGACCCAGAG TGTGACTCCTTGGCGGGGCGGCTGGTCAGACATAGTGTGCCTCCGGGCCGGAGGGCGACCCAGAG T A POMT2 Ensembl:ENSG00000009830 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77320617..77320843 26863196 MeRIP-seq:(Medium) rs1566667292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884028,Human_RBP_ID_4308024 RMVar_hsa_circ_112122,RMVar_hsa_circ_168157 73664 RMVar_ID_73664 Human_SNP_ID_561482417 m1A Human chr14 - 77321109 77321109 77321109 AGGCCGAGAAACTTCGCGCCTGGGACCTGCCGACGACTAAGGCTCAGTGAGACTCGACGAATCAG AGGCCGAGAAACTTCGCGCCTGGGACCTGCCGGCGACTAAGGCTCAGTGAGACTCGACGAATCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:77321074..77321239 26863196 MeRIP-seq:(Medium) rs1051660170 Functional Loss SNV dbSNP153 33..33 33 - - - 73665 RMVar_ID_73665 Human_SNP_ID_561487818 m1A Human chr14 - 77341901 77341901 77341901 CTATGGGGAGGTCATGCCTGTGTACCGGCGGGACAGCCACCGAGACGTGCAGGCTGGCAGCCATG CTATGGGGAGGTCATGCCTGTGTACCGGCGGGGCAGCCACCGAGACGTGCAGGCTGGCAGCCATG T C TMED8 Ensembl:ENSG00000100580 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:77341855..77341956 32194978 MeRIP-seq:(Medium) rs781360416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1539110 73666 RMVar_ID_73666 Human_SNP_ID_561496349 m1A Human chr14 - 77377445 77377445 77377445 GGCTCCAGCTCTCCATCTTCATCTGGGCCGGAATCATAATCCTCCGGGACTTCAGCCATTTGCAG GGCTCCAGCTCTCCATCTTCATCTGGGCCGGACTCATAATCCTCCGGGACTTCAGCCATTTGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:77377438..77377503 26863196 MeRIP-seq:(Medium) rs780074908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168165 73667 RMVar_ID_73667 Human_SNP_ID_561515589 m1A Human chr14 - 77458080 77458080 77458080 GGCAGCGCCTGGAAACTACTAGAAGCGGCCGCAAGCACCTCCTGGCTTGCTTTTCCCTCCACCCC GGCAGCGCCTGGAAACTACTAGAAGCGGCCGCTAGCACCTCCTGGCTTGCTTTTCCCTCCACCCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77458051..77458250 26863196 MeRIP-seq:(Medium) rs1187399243 Functional Loss SNV dbSNP153 33..33 33 - - - 73668 RMVar_ID_73668 Human_SNP_ID_561515983 m1A Human chr14 + 77459558 77459558 77459558 GTCAGGCCTCCTTTAACCTCGTATTCTCTTGCATAGAGCAGCGTATCCTCCGTTTGACTGCTGGT GTCAGGCCTCCTTTAACCTCGTATTCTCTTGCGTAGAGCAGCGTATCCTCCGTTTGACTGCTGGT A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:77459555..77459800 26863196 MeRIP-seq:(Medium) rs1031682778 Functional Loss SNV dbSNP153 33..33 33 - - - 73669 RMVar_ID_73669 Human_SNP_ID_561541130 m1A Human chr14 + 77555452 77555452 77555452 CAGGGCGCCAATGCTGTGAGCCTCATCCAGATACAAGTATGCCTTGTATTTCTTCTTGAGGGCAA CAGGGCGCCAATGCTGTGAGCCTCATCCAGATGCAAGTATGCCTTGTATTTCTTCTTGAGGGCAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:77555401..77555475 32194978 MeRIP-seq:(Medium) rs763140388 Functional Loss SNV dbSNP153 33..33 33 - - - 73670 RMVar_ID_73670 Human_SNP_ID_561557158 m1A Human chr14 + 77616552 77616552 77616552 CACGCAGCCATTCGCCCGCACCGTGCGGCGGCAGCAGCAGCCTCCGGGCTCCGGCCGCATCTTCC CACGCAGCCATTCGCCCGCACCGTGCGGCGGCGGCAGCAGCCTCCGGGCTCCGGCCGCATCTTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77616501..77616711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 73671 RMVar_ID_73671 Human_SNP_ID_561572116 m1A Human chr14 - 77674037 77674037 77674037 CTAGAGGCACCTCTCCCTGCTGTCCTCCCGAGAGATTCAATGGTAGAGCCTTGTTCTATGGAGGA CTAGAGGCACCTCTCCCTGCTGTCCTCCCGAGGGATTCAATGGTAGAGCCTTGTTCTATGGAGGA T C ALKBH1 Ensembl:ENSG00000100601 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:77673910..77674038 32194978 MeRIP-seq:(Medium) rs1566810262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168210 73672 RMVar_ID_73672 Human_SNP_ID_561581332 m1A Human chr14 - 77708150 77708150 77708150 CTCACAAAAGCAACCGGCTGATTGATACTTCTACGCAGCGCCGCAGCACCTCTCGCTGCTGAGGC CTCACAAAAGCAACCGGCTGATTGATACTTCTGCGCAGCGCCGCAGCACCTCTCGCTGCTGAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:77708076..77710615;chr14:77708076..77708269 26863196 MeRIP-seq:(Medium) rs1242108844 Functional Loss SNV dbSNP153 33..33 33 - - - 73673 RMVar_ID_73673 Human_SNP_ID_561581338 m1A Human chr14 + 77708157 77708157 77708157 CAGCGAGAGGTGCTGCGGCGCTGCGTAGAAGTATCAATCAGCCGGTTGCTTTTGTGAGAAGAATT CAGCGAGAGGTGCTGCGGCGCTGCGTAGAAGTCTCAATCAGCCGGTTGCTTTTGTGAGAAGAATT A C SLIRP Ensembl:ENSG00000119705 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:77708076..77710615 26863196 MeRIP-seq:(Medium) rs1325355865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39564,Human_RBP_ID_452761,Human_RBP_ID_1500060,Human_RBP_ID_1824952,Human_RBP_ID_2427668,Human_RBP_ID_3462683,Human_RBP_ID_4308442,Human_RBP_ID_5112430,Human_RBP_ID_5175977,Human_RBP_ID_5418318,Human_RBP_ID_5463578,Human_RBP_ID_8410930,Human_RBP_ID_9369245,Human_RBP_ID_12431070,Human_RBP_ID_18418014,Human_RBP_ID_22189028,Human_RBP_ID_22438545,Human_RBP_ID_23638302,Human_RBP_ID_26430855,Human_RBP_ID_27229243 Human_Splice_Rec_1539665,Human_Splice_Rec_1539671,Human_Splice_Rec_1539677,Human_Splice_Rec_1539683,Human_Splice_Rec_1539689,Human_Splice_Rec_1539695,Human_Splice_Rec_1539703,Human_Splice_Rec_1539707,Human_Splice_Rec_1539711,Human_Splice_Rec_1539715,Human_Splice_Rec_1539723 RMVar_hsa_circ_103903,RMVar_hsa_circ_168212 73674 RMVar_ID_73674 Human_SNP_ID_561582008 m1A Human chr14 - 77710888 77710888 77710888 CACCTACTTTTCCTTAATACTTACAAAAGGTAAAATGCACCTTCTGACATGGCCGAACTGTGCAA CACCTACTTTTCCTTAATACTTACAAAAGGTACAATGCACCTTCTGACATGGCCGAACTGTGCAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:77710768..77711757 26863196 MeRIP-seq:(Medium) rs1422859588 Functional Loss SNV dbSNP153 33..33 33 - - - 73675 RMVar_ID_73675 Human_SNP_ID_561583303 m1A Human chr14 + 77715724 77715724 77715724 AAAGTTGGTAGTTTGATTTGGAACTCATGGAAACTTTCTGAAGTTCATGATTAATCTTTTCCTAT AAAGTTGGTAGTTTGATTTGGAACTCATGGAAGCTTTCTGAAGTTCATGATTAATCTTTTCCTAT A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HeLa cell line,mRNA;HEK293T,Wild Type chr14:77715721..77715840;chr14:77715720..77715825 26863196,26863410 MeRIP-seq:(Medium) rs771917475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31026,RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 73676 RMVar_ID_73676 Human_SNP_ID_561583319 m1A Human chr14 + 77715755 77715755 77715755 AACTTTCTGAAGTTCATGATTAATCTTTTCCTATATTTTGAATTTTTAGGACAAGGAGACTGGCT AACTTTCTGAAGTTCATGATTAATCTTTTCCTGTATTTTGAATTTTTAGGACAAGGAGACTGGCT A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:77715751..77715825 26863410 MeRIP-seq:(Medium) rs373371680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31026,RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 73677 RMVar_ID_73677 Human_SNP_ID_561583990 m1A Human chr14 + 77717548 77717543 77717548 GCCAAAACTTCCGCAAACATCTGATGATGAAAAGAAAGATTTTTGAGACTGCAGCCTATTAATAA GCCAAAACTTCCGCAAACATCTGATGAT_____GAAAGATTTTTGAGACTGCAGCCTATTAATAA TGAAAA T SLIRP Ensembl:ENSG00000119705 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77717476..77717575 26863196 MeRIP-seq:(Medium) rs762750775 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_452767,Human_RBP_ID_1276850,Human_RBP_ID_1500068,Human_RBP_ID_1824958,Human_RBP_ID_3462695,Human_RBP_ID_4314692,Human_RBP_ID_5178501,Human_RBP_ID_8410951,Human_RBP_ID_9340846,Human_RBP_ID_9369249,Human_RBP_ID_12431247,Human_RBP_ID_17651411,Human_RBP_ID_17856469,Human_RBP_ID_22757927,Human_RBP_ID_22798418,Human_RBP_ID_23638314,Human_RBP_ID_25123668 Human_Splice_Rec_1539670,Human_Splice_Rec_1539676,Human_Splice_Rec_1539682,Human_Splice_Rec_1539702,Human_Splice_Rec_1539728,Human_Splice_Rec_1539732 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_124333,RMVar_hsa_circ_168213,RMVar_hsa_circ_168214 73678 RMVar_ID_73678 Human_SNP_ID_561583994 m1A Human chr14 + 77717548 77717545 77717549 GCCAAAACTTCCGCAAACATCTGATGATGAAAAGAAAGATTTTTGAGACTGCAGCCTATTAATAA GCCAAAACTTCCGCAAACATCTGATGATGA____AAAGATTTTTGAGACTGCAGCCTATTAATAA AAAAG A SLIRP Ensembl:ENSG00000119705 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77717476..77717575 26863196 MeRIP-seq:(Medium) rs1257230305 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_452767,Human_RBP_ID_1276850,Human_RBP_ID_1500068,Human_RBP_ID_1824958,Human_RBP_ID_3462695,Human_RBP_ID_4314692,Human_RBP_ID_5178501,Human_RBP_ID_8410951,Human_RBP_ID_9340846,Human_RBP_ID_9369249,Human_RBP_ID_12431247,Human_RBP_ID_17651411,Human_RBP_ID_17856469,Human_RBP_ID_22757927,Human_RBP_ID_22798418,Human_RBP_ID_23638314,Human_RBP_ID_25123668 Human_Splice_Rec_1539670,Human_Splice_Rec_1539676,Human_Splice_Rec_1539682,Human_Splice_Rec_1539702,Human_Splice_Rec_1539728,Human_Splice_Rec_1539732 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_124333,RMVar_hsa_circ_168213,RMVar_hsa_circ_168214 73679 RMVar_ID_73679 Human_SNP_ID_561583995 m1A Human chr14 + 77717548 77717548 77717548 GCCAAAACTTCCGCAAACATCTGATGATGAAAAGAAAGATTTTTGAGACTGCAGCCTATTAATAA GCCAAAACTTCCGCAAACATCTGATGATGAAAGGAAAGATTTTTGAGACTGCAGCCTATTAATAA A G SLIRP Ensembl:ENSG00000119705 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77717476..77717575 26863196 MeRIP-seq:(Medium) rs774647029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452767,Human_RBP_ID_1276850,Human_RBP_ID_1500068,Human_RBP_ID_1824958,Human_RBP_ID_3462695,Human_RBP_ID_4314692,Human_RBP_ID_5178501,Human_RBP_ID_8410951,Human_RBP_ID_9340846,Human_RBP_ID_9369249,Human_RBP_ID_12431247,Human_RBP_ID_17651411,Human_RBP_ID_17856469,Human_RBP_ID_22757927,Human_RBP_ID_22798418,Human_RBP_ID_23638314,Human_RBP_ID_25123668 Human_Splice_Rec_1539670,Human_Splice_Rec_1539676,Human_Splice_Rec_1539682,Human_Splice_Rec_1539702,Human_Splice_Rec_1539728,Human_Splice_Rec_1539732 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_124333,RMVar_hsa_circ_168213,RMVar_hsa_circ_168214 73680 RMVar_ID_73680 Human_SNP_ID_561583997 m1A Human chr14 + 77717550 77717550 77717550 CAAAACTTCCGCAAACATCTGATGATGAAAAGAAAGATTTTTGAGACTGCAGCCTATTAATAAAG CAAAACTTCCGCAAACATCTGATGATGAAAAGGAAGATTTTTGAGACTGCAGCCTATTAATAAAG A G SLIRP Ensembl:ENSG00000119705 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:77717476..77717600;chr14:77717446..77717600 26863196 MeRIP-seq:(Medium) rs772229374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452767,Human_RBP_ID_1276850,Human_RBP_ID_1500068,Human_RBP_ID_1824958,Human_RBP_ID_3462695,Human_RBP_ID_4314692,Human_RBP_ID_5178501,Human_RBP_ID_8410951,Human_RBP_ID_9340846,Human_RBP_ID_9369249,Human_RBP_ID_12431247,Human_RBP_ID_17651411,Human_RBP_ID_17856469,Human_RBP_ID_18657412,Human_RBP_ID_22757927,Human_RBP_ID_22798418,Human_RBP_ID_23638314,Human_RBP_ID_25123668 Human_Splice_Rec_1539670,Human_Splice_Rec_1539676,Human_Splice_Rec_1539682,Human_Splice_Rec_1539702,Human_Splice_Rec_1539728,Human_Splice_Rec_1539732 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_124333,RMVar_hsa_circ_168213,RMVar_hsa_circ_168214 73681 RMVar_ID_73681 Human_SNP_ID_561583998 m1A Human chr14 + 77717550 77717550 77717550 CAAAACTTCCGCAAACATCTGATGATGAAAAGAAAGATTTTTGAGACTGCAGCCTATTAATAAAG CAAAACTTCCGCAAACATCTGATGATGAAAAGTAAGATTTTTGAGACTGCAGCCTATTAATAAAG A T SLIRP Ensembl:ENSG00000119705 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:77717476..77717600;chr14:77717446..77717600 26863196 MeRIP-seq:(Medium) rs772229374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452767,Human_RBP_ID_1276850,Human_RBP_ID_1500068,Human_RBP_ID_1824958,Human_RBP_ID_3462695,Human_RBP_ID_4314692,Human_RBP_ID_5178501,Human_RBP_ID_8410951,Human_RBP_ID_9340846,Human_RBP_ID_9369249,Human_RBP_ID_12431247,Human_RBP_ID_17651411,Human_RBP_ID_17856469,Human_RBP_ID_18657412,Human_RBP_ID_22757927,Human_RBP_ID_22798418,Human_RBP_ID_23638314,Human_RBP_ID_25123668 Human_Splice_Rec_1539670,Human_Splice_Rec_1539676,Human_Splice_Rec_1539682,Human_Splice_Rec_1539702,Human_Splice_Rec_1539728,Human_Splice_Rec_1539732 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_124333,RMVar_hsa_circ_168213,RMVar_hsa_circ_168214 73682 RMVar_ID_73682 Human_SNP_ID_561585733 m1A Human chr14 + 77723273 77723273 77723273 TGCCGGATTTCATCCCTCTCACGTGCCTCCCCATCCTCTGTGTGAACAGTTGAAAAGTACTTCAC TGCCGGATTTCATCCCTCTCACGTGCCTCCCCTTCCTCTGTGTGAACAGTTGAAAAGTACTTCAC A T SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:77723176..77723328;chr14:77723135..77723320;chr14:77718434..77730900 26863196 MeRIP-seq:(Medium) rs1306002318 Functional Loss SNV dbSNP153 33..33 33 - - - 73683 RMVar_ID_73683 Human_SNP_ID_561592769 m1A Human chr14 - 77751446 77751446 77751446 TTTTGGAGATGGAGGTGCTTTTCCAGAGATCCATGTGGCCCAGTATCCACTGGATATGGGACGAA TTTTGGAGATGGAGGTGCTTTTCCAGAGATCCGTGTGGCCCAGTATCCACTGGATATGGGACGAA T C SNW1 Ensembl:ENSG00000100603 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77751426..77751450 26863196 MeRIP-seq:(Medium) rs1344578188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4303817,Human_RBP_ID_6388318,Human_RBP_ID_17856470,Human_RBP_ID_22439663,Human_RBP_ID_23638348 Human_Splice_Rec_1539736,Human_Splice_Rec_1539782,Human_Splice_Rec_1539808,Human_Splice_Rec_1539840,Human_Splice_Rec_1539850 Human_miRNA_ID_311276,Human_miRNA_ID_1157260,Human_miRNA_ID_1336129,Human_miRNA_ID_1563260,Human_miRNA_ID_2506609,Human_miRNA_ID_3043180 RMVar_hsa_circ_32238,RMVar_hsa_circ_94961,RMVar_hsa_circ_82103,RMVar_hsa_circ_168227,RMVar_hsa_circ_74560,RMVar_hsa_circ_168228 73684 RMVar_ID_73684 Human_SNP_ID_561595335 m1A Human chr14 + 77761043 77761043 77761043 TGTGCCCCGGGTCAGGTCACCGCCCGGAGGGTATGGGAAGAGAAATGAAGAAGACTGGTACTCCC TGTGCCCCGGGTCAGGTCACCGCCCGGAGGGTGTGGGAAGAGAAATGAAGAAGACTGGTACTCCC A G SLIRP,C14orf178 Ensembl:ENSG00000119705,Ensembl:ENSG00000197734 Protein coding,Protein coding 3'UTR,start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77761042..77761128 26863196 MeRIP-seq:(Medium) rs756756837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1539855,Human_Splice_Rec_1539859,Human_Splice_Rec_1539861,Human_Splice_Rec_1539865,Human_Splice_Rec_1539867 73685 RMVar_ID_73685 Human_SNP_ID_561595336 m1A Human chr14 + 77761043 77761043 77761043 TGTGCCCCGGGTCAGGTCACCGCCCGGAGGGTATGGGAAGAGAAATGAAGAAGACTGGTACTCCC TGTGCCCCGGGTCAGGTCACCGCCCGGAGGGTTTGGGAAGAGAAATGAAGAAGACTGGTACTCCC A T SLIRP,C14orf178 Ensembl:ENSG00000119705,Ensembl:ENSG00000197734 Protein coding,Protein coding 3'UTR,start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77761042..77761128 26863196 MeRIP-seq:(Medium) rs756756837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1539855,Human_Splice_Rec_1539859,Human_Splice_Rec_1539861,Human_Splice_Rec_1539865,Human_Splice_Rec_1539867 73686 RMVar_ID_73686 Human_SNP_ID_561595340 m1A Human chr14 + 77761058 77761056 77761059 GTCACCGCCCGGAGGGTATGGGAAGAGAAATGAAGAAGACTGGTACTCCCAGACCCTTCCGTATC GTCACCGCCCGGAGGGTATGGGAAGAGAAAT___GAAGACTGGTACTCCCAGACCCTTCCGTATC TGAA T SLIRP,C14orf178 Ensembl:ENSG00000119705,Ensembl:ENSG00000197734 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77761055..77761150 26863196 MeRIP-seq:(Medium) rs769784069 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1539855,Human_Splice_Rec_1539859,Human_Splice_Rec_1539861,Human_Splice_Rec_1539865,Human_Splice_Rec_1539867 73687 RMVar_ID_73687 Human_SNP_ID_561635035 m1A Human chr14 + 77923304 77923304 77923304 GAGAGGGTAAGCCAGGTGAAGGGGAGATGGCAAGAATGCTCCTGGCAGCAGGAATAGCATGTGCA GAGAGGGTAAGCCAGGTGAAGGGGAGATGGCAGGAATGCTCCTGGCAGCAGGAATAGCATGTGCA A G ADCK1 Ensembl:ENSG00000063761 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:77923301..77923424 26863196 MeRIP-seq:(Medium) rs867075070 Functional Loss SNV dbSNP153 33..33 33 - - - 73688 RMVar_ID_73688 Human_SNP_ID_561636234 m1A Human chr14 + 77928127 77928127 77928127 GGTGTGTTTTGGAAGTAAGATTGAGTTTCTGTAGGATTGGATGTGGAGAGAAGGGAAAGGGCAGG GGTGTGTTTTGGAAGTAAGATTGAGTTTCTGTGGGATTGGATGTGGAGAGAAGGGAAAGGGCAGG A G ADCK1 Ensembl:ENSG00000063761 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:77928125..77928241 26863196 MeRIP-seq:(Medium) rs976587753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86450,RMVar_hsa_circ_76848,RMVar_hsa_circ_168231,RMVar_hsa_circ_168232 73689 RMVar_ID_73689 Human_SNP_ID_561958860 m1A Human chr14 + 79279451 79279451 79279451 CAGGCGCCCGCCCGCCTCTCGGCCACCTCTGCAGCCTGCCAGGCACCTCCTCTTGCGCTCTCGCT CAGGCGCCCGCCCGCCTCTCGGCCACCTCTGCCGCCTGCCAGGCACCTCCTCTTGCGCTCTCGCT A C NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:79279407..79279510 26863196 MeRIP-seq:(Medium) rs1440751553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4303845,Human_RBP_ID_5418329,Human_RBP_ID_5493950,Human_RBP_ID_12431674 RMVar_hsa_circ_12943 73690 RMVar_ID_73690 Human_SNP_ID_562097401 m1A Human chr14 + 79845607 79845607 79845607 CGACCCAGAGAGACAGAGAGAGAGAGAGACAGAGAGAGAGACGGAGACGGGGAGAGAGACGGAGA CGACCCAGAGAGACAGAGAGAGAGAGAGACAGGGAGAGAGACGGAGACGGGGAGAGAGACGGAGA A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:79845527..79845758 26863196 MeRIP-seq:(Medium) rs568537368 Functional Loss SNV dbSNP153 33..33 33 - - - 73691 RMVar_ID_73691 Human_SNP_ID_562346826 m1A Human chr14 + 80862847 80862847 80862847 CTTTCTGTGCGCATCTCTCTCTCCAGTTCCTGAAGCCGCCGCTCCACCCGATCTGAAACCTTAAT CTTTCTGTGCGCATCTCTCTCTCCAGTTCCTGGAGCCGCCGCTCCACCCGATCTGAAACCTTAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:80862797..80862862 26863196 MeRIP-seq:(Medium) rs1366852827 Functional Loss SNV dbSNP153 33..33 33 - - - 73692 RMVar_ID_73692 Human_SNP_ID_562365116 m1A Human chr14 - 80941674 80941674 80941674 GAGCACAGTCGGTTGAGTCGCTGCGTTTGGTCAGTTGCACCTTCTGGGTCACTGGTAGCCGCGGG GAGCACAGTCGGTTGAGTCGCTGCGTTTGGTCGGTTGCACCTTCTGGGTCACTGGTAGCCGCGGG T C CEP128 Ensembl:ENSG00000100629 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:80941554..80941708 26863196 MeRIP-seq:(Medium) rs962786945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5463802,Human_RBP_ID_5522859,Human_RBP_ID_18980918 Human_Splice_Rec_1540451,Human_Splice_Rec_1540525,Human_Splice_Rec_1540575,Human_Splice_Rec_1540583 RMVar_hsa_circ_355656 73693 RMVar_ID_73693 Human_SNP_ID_562365118 m1A Human chr14 + 80941676 80941676 80941676 CGCGGCTACCAGTGACCCAGAAGGTGCAACTGACCAAACGCAGCGACTCAACCGACTGTGCTCTC CGCGGCTACCAGTGACCCAGAAGGTGCAACTGTCCAAACGCAGCGACTCAACCGACTGTGCTCTC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:80941551..80941711 26863196 MeRIP-seq:(Medium) rs1352524863 Functional Loss SNV dbSNP153 33..33 33 - - - 73694 RMVar_ID_73694 Human_SNP_ID_562422917 m1A Human chr14 + 81192471 81192471 81192471 GATATAATTTATCAGTGTTGTACCAACTAAAAAAGGAAATAATCAAGTAGATTATTTTAAGTATG GATATAATTTATCAGTGTTGTACCAACTAAAAGAGGAAATAATCAAGTAGATTATTTTAAGTATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:81192469..81192638 26863196 MeRIP-seq:(Medium) rs747511245 Functional Loss SNV dbSNP153 33..33 33 - - - 73695 RMVar_ID_73695 Human_SNP_ID_562422925 m1A Human chr14 - 81192486 81192486 81192486 GTAAGTTTCTAGTAACATACTTAAAATAATCTACTTGATTATTTCCTTTTTTAGTTGGTACAACA GTAAGTTTCTAGTAACATACTTAAAATAATCTGCTTGATTATTTCCTTTTTTAGTTGGTACAACA T C GTF2A1 Ensembl:ENSG00000165417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:81192484..81192643 26863196 MeRIP-seq:(Medium) rs1446551585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304727,RMVar_hsa_circ_350628,RMVar_hsa_circ_356259,RMVar_hsa_circ_311567,RMVar_hsa_circ_168299,RMVar_hsa_circ_168300 73696 RMVar_ID_73696 Human_SNP_ID_562430129 m1A Human chr14 - 81220414 81220414 81220414 TGCAGCAACGGCCGGACCGGGCGGGGGCGGGGACGGCGGCGACTCCCGGCCTCGACTCTTCAGCC TGCAGCAACGGCCGGACCGGGCGGGGGCGGGGTCGGCGGCGACTCCCGGCCTCGACTCTTCAGCC T A GTF2A1 Ensembl:ENSG00000165417 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:81220383..81220454 26863196 MeRIP-seq:(Medium) rs981418356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18457861,Human_RBP_ID_23639190 73697 RMVar_ID_73697 Human_SNP_ID_562430268 m1A Human chr14 + 81220740 81220737 81220741 CCCGCAGCTGAAAACCTCGAGAATCGCCTTAAAAAAAAAAAAAAAGCCACGACCCTTCAGGGGTC CCCGCAGCTGAAAACCTCGAGAATCGCCTT____AAAAAAAAAAAGCCACGACCCTTCAGGGGTC TAAAA T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:81220701..81220900 26863196 MeRIP-seq:(Medium) rs879011381 Functional Loss DEL dbSNP153 31..34 33 - - - 73698 RMVar_ID_73698 Human_SNP_ID_562430275 m1A Human chr14 + 81220740 81220740 81220740 CCCGCAGCTGAAAACCTCGAGAATCGCCTTAAAAAAAAAAAAAAAGCCACGACCCTTCAGGGGTC CCCGCAGCTGAAAACCTCGAGAATCGCCTTAAGAAAAAAAAAAAAGCCACGACCCTTCAGGGGTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:81220701..81220900 26863196 MeRIP-seq:(Medium) rs1451188655 Functional Loss SNV dbSNP153 33..33 33 - - - 73699 RMVar_ID_73699 Human_SNP_ID_562430315 m1A Human chr14 - 81220837 81220837 81220837 GGAGCTGCAGCCGGTGGCGGCAGCGGCGGCGCAGGGAGCGGTGACCGGTGGTGGTTTCCCTCCTT GGAGCTGCAGCCGGTGGCGGCAGCGGCGGCGCGGGGAGCGGTGACCGGTGGTGGTTTCCCTCCTT T C GTF2A1 Ensembl:ENSG00000165417 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:81220763..81220944;chr14:81220657..81220950 26863196 MeRIP-seq:(Medium) rs1416895182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_453014,Human_RBP_ID_4304045,Human_RBP_ID_9324079,Human_RBP_ID_23127062 73700 RMVar_ID_73700 Human_SNP_ID_562430321 m1A Human chr14 - 81220848 81220848 81220848 ACCGGACGGCTGGAGCTGCAGCCGGTGGCGGCAGCGGCGGCGCAGGGAGCGGTGACCGGTGGTGG ACCGGACGGCTGGAGCTGCAGCCGGTGGCGGCGGCGGCGGCGCAGGGAGCGGTGACCGGTGGTGG T C GTF2A1 Ensembl:ENSG00000165417 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:81220676..81220900 26863196 MeRIP-seq:(Medium) rs1389065419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231745,Human_RBP_ID_453014,Human_RBP_ID_4304045,Human_RBP_ID_9324079 73701 RMVar_ID_73701 Human_SNP_ID_562430328 m1A Human chr14 + 81220864 81220864 81220864 CTCCCTGCGCCGCCGCTGCCGCCACCGGCTGCAGCTCCAGCCGTCCGGTCCGCCCGCTTCTCTCC CTCCCTGCGCCGCCGCTGCCGCCACCGGCTGCGGCTCCAGCCGTCCGGTCCGCCCGCTTCTCTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:81220522..81220896 26863196 MeRIP-seq:(Medium) rs1423988938 Functional Loss SNV dbSNP153 33..33 33 - - - 73702 RMVar_ID_73702 Human_SNP_ID_562507064 m1A Human chr14 - 81533793 81533793 81533793 GAGGCGGCGGTGGTGGCTGAGTCCGTGGTGGCAGAGGCGAAGGCGACAGCTCTAGGGGTTGGCAC GAGGCGGCGGTGGTGGCTGAGTCCGTGGTGGCCGAGGCGAAGGCGACAGCTCTAGGGGTTGGCAC T G SEL1L Ensembl:ENSG00000071537 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:81533676..81533850 26863196 MeRIP-seq:(Medium) rs1566631809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230881,Human_RBP_ID_453113,Human_RBP_ID_812744,Human_RBP_ID_4308034,Human_RBP_ID_8798160,Human_RBP_ID_22438808 RMVar_hsa_circ_121508,RMVar_hsa_circ_97633,RMVar_hsa_circ_168322,RMVar_hsa_circ_168323 73703 RMVar_ID_73703 Human_SNP_ID_563516609 m1A Human chr14 + 85533244 85533244 85533244 ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGAGGCGATCCCGCGAATTCATTACTGTAAACATA ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGCGGCGATCCCGCGAATTCATTACTGTAAACATA A C FLRT2 Ensembl:ENSG00000185070 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:85533198..85533297 26863196 MeRIP-seq:(Medium) rs1030876222 Functional Loss SNV dbSNP153 33..33 33 - - - 73704 RMVar_ID_73704 Human_SNP_ID_563516610 m1A Human chr14 + 85533244 85533244 85533244 ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGAGGCGATCCCGCGAATTCATTACTGTAAACATA ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGGGGCGATCCCGCGAATTCATTACTGTAAACATA A G FLRT2 Ensembl:ENSG00000185070 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:85533198..85533297 26863196 MeRIP-seq:(Medium) rs1030876222 Functional Loss SNV dbSNP153 33..33 33 - - - 73705 RMVar_ID_73705 Human_SNP_ID_563516611 m1A Human chr14 + 85533244 85533244 85533244 ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGAGGCGATCCCGCGAATTCATTACTGTAAACATA ACGGAGGGAGAGGAGGAGCGCGGGAGCTGCGGTGGCGATCCCGCGAATTCATTACTGTAAACATA A T FLRT2 Ensembl:ENSG00000185070 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:85533198..85533297 26863196 MeRIP-seq:(Medium) rs1030876222 Functional Loss SNV dbSNP153 33..33 33 - - - 73706 RMVar_ID_73706 Human_SNP_ID_564262217 m1A Human chr14 + 88466557 88466555 88466558 CCCTAGATTTGACATTTTGGAAGTTCACTGTAAGAAGAGACCCCAAAAAGAAGGAAAAGGGAAAG CCCTAGATTTGACATTTTGGAAGTTCACTGT___AAGAGACCCCAAAAAGAAGGAAAAGGGAAAG TAAG T SPATA7 Ensembl:ENSG00000042317 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:88466510..88466593 32194978 MeRIP-seq:(Medium) rs1405056280 Functional Loss DEL dbSNP153 32..34 33 - - - 73707 RMVar_ID_73707 Human_SNP_ID_564265587 m1A Human chr14 + 88479048 88479045 88479048 GCCTGACGTGGTGAGGTCGGACTCCGACATGGAGGGCATCAGCAGCCCGTCTCTCCAGGGCCGCT GCCTGACGTGGTGAGGTCGGACTCCGACAT___GGGCATCAGCAGCCCGTCTCTCCAGGGCCGCT TGGA T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:88479012..88479159 26863196 MeRIP-seq:(Medium) rs1566811631 Functional Loss DEL dbSNP153 31..33 33 - - - 73708 RMVar_ID_73708 Human_SNP_ID_564287195 m1A Human chr14 + 88563078 88563078 88563078 GGTGTCCCGGCTGCGGGGTAGGAGTCCGCGGCAGCCTCCGGGTAAGCCAAGCGCCGCGCAGTGCT GGTGTCCCGGCTGCGGGGTAGGAGTCCGCGGCGGCCTCCGGGTAAGCCAAGCGCCGCGCAGTGCT A G ZC3H14 Ensembl:ENSG00000100722 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:88563001..88563342 26863196 MeRIP-seq:(Medium) rs1322470713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231606,Human_RBP_ID_4308455,Human_RBP_ID_9369271,Human_RBP_ID_18418015 Human_Splice_Rec_1542819,Human_Splice_Rec_1542845,Human_Splice_Rec_1542853,Human_Splice_Rec_1542889,Human_Splice_Rec_1542897,Human_Splice_Rec_1542925,Human_Splice_Rec_1542937,Human_Splice_Rec_1542961,Human_Splice_Rec_1542969,Human_Splice_Rec_1543001,Human_Splice_Rec_1543033 73709 RMVar_ID_73709 Human_SNP_ID_564287241 m1A Human chr14 + 88563152 88563152 88563152 CACGCCGCAGAGCCATGGAGATCGGCACCGAGATCAGCCGCAAGATCCGGGTGAGGCCCGTGCCG CACGCCGCAGAGCCATGGAGATCGGCACCGAGCTCAGCCGCAAGATCCGGGTGAGGCCCGTGCCG A C ZC3H14 Ensembl:ENSG00000100722 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:88563051..88563175 26863410 MeRIP-seq:(Medium) rs757192945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308455,Human_RBP_ID_18418015 Human_Splice_Rec_1542819,Human_Splice_Rec_1542845,Human_Splice_Rec_1542853,Human_Splice_Rec_1542889,Human_Splice_Rec_1542897,Human_Splice_Rec_1542925,Human_Splice_Rec_1542937,Human_Splice_Rec_1542961,Human_Splice_Rec_1542969,Human_Splice_Rec_1543001,Human_Splice_Rec_1543033 73710 RMVar_ID_73710 Human_SNP_ID_564351772 m1A Human chr14 + 88824763 88824763 88824763 GCTCCTGGCCTGGAGCTATTTTAGGCGCAGGAAGTTCCAGCTCTGCGCCGATCTATGCACGCAGA GCTCCTGGCCTGGAGCTATTTTAGGCGCAGGACGTTCCAGCTCTGCGCCGATCTATGCACGCAGA A C TTC8 Ensembl:ENSG00000165533 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:88824710..88824810 32194978 MeRIP-seq:(Medium) rs756206583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308456 Human_Splice_Rec_1543519,Human_Splice_Rec_1543535,Human_Splice_Rec_1543561,Human_Splice_Rec_1543591,Human_Splice_Rec_1543617,Human_Splice_Rec_1543645,Human_Splice_Rec_1543649,Human_Splice_Rec_1543675,Human_Splice_Rec_1543685,Human_Splice_Rec_1543709,Human_Splice_Rec_1543737,Human_Splice_Rec_1543747,Human_Splice_Rec_1543775,Human_Splice_Rec_1543799,Human_Splice_Rec_1543809 73711 RMVar_ID_73711 Human_SNP_ID_564351970 m1A Human chr14 + 88825443 88825443 88825443 GAAGCTCTAATTGTAGGAGGGAGAAATGGGAAAGAAAGGCTCCTTACAAGAAGGAATGATGGCAT GAAGCTCTAATTGTAGGAGGGAGAAATGGGAAGGAAAGGCTCCTTACAAGAAGGAATGATGGCAT A G TTC8 Ensembl:ENSG00000165533 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:88825438..88825549 26863196 MeRIP-seq:(Medium) rs548617419 Functional Loss SNV dbSNP153 33..33 33 - - - 73712 RMVar_ID_73712 Human_SNP_ID_564355354 m1A Human chr14 + 88841062 88841062 88841062 TTCACAGGCCAATCACACAAGCTGGAAGACCCATTACAGGTTTCCTCAGGCCCAGCACGCAGAGT TTCACAGGCCAATCACACAAGCTGGAAGACCCGTTACAGGTTTCCTCAGGCCCAGCACGCAGAGT A G TTC8 Ensembl:ENSG00000165533 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:88840941..88841061 32194978 MeRIP-seq:(Medium) rs1188208020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1543526,Human_Splice_Rec_1543540,Human_Splice_Rec_1543566,Human_Splice_Rec_1543596,Human_Splice_Rec_1543624,Human_Splice_Rec_1543654,Human_Splice_Rec_1543680,Human_Splice_Rec_1543690,Human_Splice_Rec_1543714,Human_Splice_Rec_1543754,Human_Splice_Rec_1543780,Human_Splice_Rec_1543804,Human_Splice_Rec_1543814,Human_Splice_Rec_1543832 RMVar_hsa_circ_356971,RMVar_hsa_circ_360914,RMVar_hsa_circ_364419,RMVar_hsa_circ_360879,RMVar_hsa_circ_16863,RMVar_hsa_circ_51763,RMVar_hsa_circ_292633,RMVar_hsa_circ_168442,RMVar_hsa_circ_45824,RMVar_hsa_circ_168443,RMVar_hsa_circ_372294 73713 RMVar_ID_73713 Human_SNP_ID_564388963 m1A Human chr14 + 88979155 88979155 88979155 GCTCGCTTAGCATGCGAGAGGTAGTGGGATCGATGCCCGCATTCTCCATACGTTACCATTTGAAT GCTCGCTTAGCATGCGAGAGGTAGTGGGATCGGTGCCCGCATTCTCCATACGTTACCATTTGAAT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs552708794 Functional Loss SNV dbSNP153 33..33 33 - - - 73714 RMVar_ID_73714 Human_SNP_ID_564388993 m1A Human chr14 - 88979182 88979182 88979182 GTCTGTGATCTTGTTTGGAGACCCAAGATTCAAATGGTAACGTATGGAGAATGCGGGCATCGATC GTCTGTGATCTTGTTTGGAGACCCAAGATTCATATGGTAACGTATGGAGAATGCGGGCATCGATC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:88979111..88979225 26863196 MeRIP-seq:(Medium) rs1219306079 Functional Loss SNV dbSNP153 33..33 33 - - - 73715 RMVar_ID_73715 Human_SNP_ID_564465661 m1A Human chr14 - 89291618 89291618 89291618 GTGGCCGGCCACAGATTTGCATTGCCAAAGACAGGACCCCAGGGCAGCAAAGCAGAATGGCAGAC GTGGCCGGCCACAGATTTGCATTGCCAAAGACGGGACCCCAGGGCAGCAAAGCAGAATGGCAGAC T C FOXN3 Ensembl:ENSG00000053254 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:89291603..89291668 26863196 MeRIP-seq:(Medium) rs1566948532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22355044 RMVar_hsa_circ_353413,RMVar_hsa_circ_45700,RMVar_hsa_circ_319601,RMVar_hsa_circ_335171,RMVar_hsa_circ_168457 73716 RMVar_ID_73716 Human_SNP_ID_564477465 m1A Human chr14 + 89336140 89336139 89336140 TCGATTTTGTCTAAAACAGAAGTGATCCTTACACACACACACACACACACACACACACACACACA TCGATTTTGTCTAAAACAGAAGTGATCCTTAC_CACACACACACACACACACACACACACACACA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:89336121..89336317 26863196 MeRIP-seq:(Medium) rs1566959941 Functional Loss DEL dbSNP153 33..33 33 - - - 73717 RMVar_ID_73717 Human_SNP_ID_564540773 m1A Human chr14 - 89578522 89578521 89578522 ACAAGAGTTCTGTGTCGGTCAGCCTAAGTTTGAGATGCCTGTTGCACGTGTCAGGGAGTGCTGCT ACAAGAGTTCTGTGTCGGTCAGCCTAAGTTTG_GATGCCTGTTGCACGTGTCAGGGAGTGCTGCT CT C AL137230.3,FOXN3 Ensembl:ENSG00000259053,Ensembl:ENSG00000053254 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:89578520..89578603 26863196 MeRIP-seq:(Medium) rs1422121819 Functional Loss DEL dbSNP153 33..33 33 - - - 73718 RMVar_ID_73718 Human_SNP_ID_564541025 m1A Human chr14 - 89579569 89579569 89579569 TGGGAGATGAAATGGCAGGATCCCATCACCTCAGGGCTTATGGGCAAGAGAAATGTGGATTTTAT TGGGAGATGAAATGGCAGGATCCCATCACCTCGGGGCTTATGGGCAAGAGAAATGTGGATTTTAT T C AL137230.3,FOXN3 Ensembl:ENSG00000259053,Ensembl:ENSG00000053254 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:89579564..89579774 26863196 MeRIP-seq:(Medium) rs986575327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18436139 73719 RMVar_ID_73719 Human_SNP_ID_564590989 m1A Human chr14 - 89795584 89795584 89795584 CGGCTCACTGCAACTTCCGCCTCCTGGGATCAAGTGATTCTCCTGCCTTAGCCTCCTGAGTATCT CGGCTCACTGCAACTTCCGCCTCCTGGGATCAGGTGATTCTCCTGCCTTAGCCTCCTGAGTATCT T C AL137230.3,EFCAB11 Ensembl:ENSG00000259053,Ensembl:ENSG00000140025 lincRNA,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1466728248 Functional Loss SNV dbSNP153 33..33 33 - - - 73720 RMVar_ID_73720 Human_SNP_ID_564627419 m1A Human chr14 + 89955969 89955969 89955969 GATCCGAGGCAAGCGTTGGTTCTGTGCGCCTCAGGTACGTGTTGGGCGGCAGTGGGCGCGGACTC GATCCGAGGCAAGCGTTGGTTCTGTGCGCCTCCGGTACGTGTTGGGCGGCAGTGGGCGCGGACTC A C TDP1 Ensembl:ENSG00000042088 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:89955954..89956149 26863196 MeRIP-seq:(Medium) rs886050882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418175,Human_RBP_ID_27837246 Human_Splice_Rec_1544145,Human_Splice_Rec_1544179,Human_Splice_Rec_1544191,Human_Splice_Rec_1544223,Human_Splice_Rec_1544253,Human_Splice_Rec_1544267 Clinvar_Rec_338 73721 RMVar_ID_73721 Human_SNP_ID_564627421 m1A Human chr14 - 89955972 89955972 89955972 ACCGAGTCCGCGCCCACTGCCGCCCAACACGTACCTGAGGCGCACAGAACCAACGCTTGCCTCGG ACCGAGTCCGCGCCCACTGCCGCCCAACACGTTCCTGAGGCGCACAGAACCAACGCTTGCCTCGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:89955953..89956164 26863196 MeRIP-seq:(Medium) rs902083021 Functional Loss SNV dbSNP153 33..33 33 - - - 73722 RMVar_ID_73722 Human_SNP_ID_564627448 m1A Human chr14 - 89956013 89956013 89956013 GAGCAGGATCCCGGGCCCGACCGCAGCCCGCGAGAGACCGCACCGAGTCCGCGCCCACTGCCGCC GAGCAGGATCCCGGGCCCGACCGCAGCCCGCGGGAGACCGCACCGAGTCCGCGCCCACTGCCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:89955965..89956163 26863196 MeRIP-seq:(Medium) rs1278409265 Functional Loss SNV dbSNP153 33..33 33 - - - 73723 RMVar_ID_73723 Human_SNP_ID_326416567 m1A Human chr7 - 75026801 75026801 75026801 ACCGTCAGGGGGAAATGACAGAAAGGAAAATCAAGGCCTTGCAAGGTCAGAAAGGGGACTCAGGG ACCGTCAGGGGGAAATGACAGAAAGGAAAATCGAGGCCTTGCAAGGTCAGAAAGGGGACTCAGGG T C RF00017-071,lnc-RCC1L-1,RF00017-4513 RNACentral:URS00009310A4,RNACentral:URS00009AF63A,RNACentral:URS000090EECB SRP RNA,lincRNA,SRP RNA intron,exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:75026751..75026850 26863196 MeRIP-seq:(Medium) rs1158177729 Functional Loss SNV dbSNP153 33..33 33 - - - 73724 RMVar_ID_73724 Human_SNP_ID_326425915 m1A Human chr7 + 75066689 75066689 75066689 AACTCACCTCCTTCCCTGTCAGTCAACACAAGAGAGTGAGCTCGGCCGCAGGAGACCTGCAGCAC AACTCACCTCCTTCCCTGTCAGTCAACACAAGTGAGTGAGCTCGGCCGCAGGAGACCTGCAGCAC A T RF00017-6354,RF00017-4525 RNACentral:URS0000951611,RNACentral:URS00009368C0 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:75066651..75066700 32194978 MeRIP-seq:(Medium) rs889434318 Functional Loss SNV dbSNP153 33..33 33 - - - 73725 RMVar_ID_73725 Human_SNP_ID_326427084 m1A Human chr7 - 75070769 75070769 75070769 TCAGTTCATGCTTTGTGGGAACTGCTTTTCAGATTTCATCTGCTGCTTGCGGCTATGGATTCACA TCAGTTCATGCTTTGTGGGAACTGCTTTTCAGGTTTCATCTGCTGCTTGCGGCTATGGATTCACA T C RCC1L Ensembl:ENSG00000274523 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:75070723..75073568 32194978 MeRIP-seq:(Medium) rs1554445971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952540,Human_RBP_ID_3100190 Human_Splice_Rec_877560,Human_Splice_Rec_877580,Human_Splice_Rec_877614,Human_Splice_Rec_877630,Human_Splice_Rec_877646 Human_miRNA_ID_2099526,Human_miRNA_ID_2105481,Human_miRNA_ID_2111425,Human_miRNA_ID_2163972,Human_miRNA_ID_2595198,Human_miRNA_ID_2738141,Human_miRNA_ID_3038739 RMVar_hsa_circ_278713,RMVar_hsa_circ_345286,RMVar_hsa_circ_345479,RMVar_hsa_circ_361740,RMVar_hsa_circ_332456,RMVar_hsa_circ_296753,RMVar_hsa_circ_357653 73726 RMVar_ID_73726 Human_SNP_ID_326428105 m1A Human chr7 - 75073745 75073745 75073745 GATGGCGGCGCCCAGAGGCTGCTGAGGCGCGGAACGGAGGATGGCGCTGGTGGCGTTGGTGGCTG GATGGCGGCGCCCAGAGGCTGCTGAGGCGCGGTACGGAGGATGGCGCTGGTGGCGTTGGTGGCTG T A RCC1L Ensembl:ENSG00000274523 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr7:75073605..75073775;chr7:75073371..75073825;chr7:75073601..75073800 26863196 MeRIP-seq:(Medium) rs1462175075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956420,Human_RBP_ID_5123407,Human_RBP_ID_9311321,Human_RBP_ID_9337187,Human_RBP_ID_9354762,Human_RBP_ID_17166884,Human_RBP_ID_22463552,Human_RBP_ID_27842906 73727 RMVar_ID_73727 Human_SNP_ID_326432073 m1A Human chr7 + 75092637 75092637 75092637 AGGGCGAGTGGCGAGCAGGGGCCTCGGCCGCCACCCACACGCCCCGAAGCGTGCTCGTCCCCCGC AGGGCGAGTGGCGAGCAGGGGCCTCGGCCGCCGCCCACACGCCCCGAAGCGTGCTCGTCCCCCGC A G GTF2IRD2B Ensembl:ENSG00000174428 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:75092588..75092763 26863196 MeRIP-seq:(Medium) rs1375977286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18426032,Human_RBP_ID_22730262 73728 RMVar_ID_73728 Human_SNP_ID_326464294 m1A Human chr7 + 75369226 75369226 75369226 CTGGAGTGCAATGAGGCGATCTCGCCTCATGCAACCTCCATCTCCCGGGTTCAAGCAATTCTCCT CTGGAGTGCAATGAGGCGATCTCGCCTCATGCGACCTCCATCTCCCGGGTTCAAGCAATTCTCCT A G STAG3L1 Ensembl:ENSG00000205583 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1332191695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577172 73729 RMVar_ID_73729 Human_SNP_ID_326474555 m1A Human chr7 - 75424201 75424201 75424201 TTTCTTAGATGCTGCCTCGAACTCTGTCACTGAGACCCCACCTACCACTCAGCCTTCATTTACCT TTTCTTAGATGCTGCCTCGAACTCTGTCACTGGGACCCCACCTACCACTCAGCCTTCATTTACCT T C POM121C Ensembl:ENSG00000272391 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:75424116..75424317 26863196 MeRIP-seq:(Medium) rs1554471360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956035,Human_RBP_ID_17426170,Human_RBP_ID_18104012,Human_RBP_ID_18960133,Human_RBP_ID_27533563 Human_Splice_Rec_878290,Human_Splice_Rec_878316,Human_Splice_Rec_878324,Human_Splice_Rec_878334 73730 RMVar_ID_73730 Human_SNP_ID_326479461 m1A Human chr7 + 75442303 75442303 75442303 CCAGGCCTATTCCGCAGGTCCTGGCCCTCCGGAGCGGGGGCGGGCTGCGGCGGCCCGGGCTTGCC CCAGGCCTATTCCGCAGGTCCTGGCCCTCCGGCGCGGGGGCGGGCTGCGGCGGCCCGGGCTTGCC A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:75442201..75442350 26863410 MeRIP-seq:(Medium) rs1378088362 Functional Loss SNV dbSNP153 33..33 33 - - - 73731 RMVar_ID_73731 Human_SNP_ID_326490427 m1A Human chr7 + 75486198 75486198 75486198 TCCCGCCCGCCTAGGTGCTGGTCCGGGCGGTCAGCATCCAGCCCCGCAGACTCGGTGATTCTCGT TCCCGCCCGCCTAGGTGCTGGTCCGGGCGGTCCGCATCCAGCCCCGCAGACTCGGTGATTCTCGT A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:75486149..75486245 26863196 MeRIP-seq:(Medium) rs587678149 Functional Loss SNV dbSNP153 33..33 33 - - - 73732 RMVar_ID_73732 Human_SNP_ID_326502861 m1A Human chr7 + 75527870 75527870 75527870 TTCGCCTCCGCCGCCACTTCGCCTCCGCCGCCACCTCAGCCGACTCCCTCCCGGCCCCTCTGGCC TTCGCCTCCGCCGCCACTTCGCCTCCGCCGCCCCCTCAGCCGACTCCCTCCCGGCCCCTCTGGCC A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:75525949..75528096;chr7:75527683..75528087 26863196 MeRIP-seq:(Medium) rs1431701689 Functional Loss SNV dbSNP153 33..33 33 - - - 73733 RMVar_ID_73733 Human_SNP_ID_326510116 m1A Human chr7 - 75556090 75556090 75556090 GGACAGCCTGGTGAGTGGCGCAGCTCATAGGGAGGAGGAATTATCTGCTCTTCGGAAAGAACTGC GGACAGCCTGGTGAGTGGCGCAGCTCATAGGGGGGAGGAATTATCTGCTCTTCGGAAAGAACTGC T C HIP1 Ensembl:ENSG00000127946 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:75556088..75556215 26863196 MeRIP-seq:(Medium) rs1554493239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_878526,Human_Splice_Rec_878582,Human_Splice_Rec_878634 Human_miRNA_ID_2251805,Human_miRNA_ID_2251806 RMVar_hsa_circ_51073,RMVar_hsa_circ_52399,RMVar_hsa_circ_3532,RMVar_hsa_circ_366729,RMVar_hsa_circ_70071,RMVar_hsa_circ_329915,RMVar_hsa_circ_338648,RMVar_hsa_circ_71424,RMVar_hsa_circ_267604 73734 RMVar_ID_73734 Human_SNP_ID_326531229 m1A Human chr7 - 75638679 75638679 75638679 CGTGCCCTCCGGAGCCCCCTGCCCGCACACCTACAGGAGATCGATGGAAGATGTGTGGGGCTGAG CGTGCCCTCCGGAGCCCCCTGCCCGCACACCTGCAGGAGATCGATGGAAGATGTGTGGGGCTGAG T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75638673..75638773 26863196 MeRIP-seq:(Medium) rs1181256317 Functional Loss SNV dbSNP153 33..33 33 - - - 73735 RMVar_ID_73735 Human_SNP_ID_326531359 m1A Human chr7 + 75639119 75639119 75639119 CCCCCCCACCCCTGGAGATCCCGCTTCCCCCAAAGCTGCTCCCGGCTAATCGCGCCCCGAGGGTG CCCCCCCACCCCTGGAGATCCCGCTTCCCCCAGAGCTGCTCCCGGCTAATCGCGCCCCGAGGGTG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75639080..75639221 26863196 MeRIP-seq:(Medium) rs1456892348 Functional Loss SNV dbSNP153 33..33 33 - - - 73736 RMVar_ID_73736 Human_SNP_ID_326542091 m1A Human chr7 - 75679567 75679567 75679567 GTGGCAAGTCCTGGAAAACAAGCTCTAGTTAGATGGGAACTAACCAGAAAAGTAAAAAAGTAAAT GTGGCAAGTCCTGGAAAACAAGCTCTAGTTAGGTGGGAACTAACCAGAAAAGTAAAAAAGTAAAT T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75679562..75679743 26863196 MeRIP-seq:(Medium) rs1211442364 Functional Loss SNV dbSNP153 33..33 33 - - - 73737 RMVar_ID_73737 Human_SNP_ID_326542092 m1A Human chr7 - 75679567 75679567 75679567 GTGGCAAGTCCTGGAAAACAAGCTCTAGTTAGATGGGAACTAACCAGAAAAGTAAAAAAGTAAAT GTGGCAAGTCCTGGAAAACAAGCTCTAGTTAGCTGGGAACTAACCAGAAAAGTAAAAAAGTAAAT T G HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75679562..75679743 26863196 MeRIP-seq:(Medium) rs1211442364 Functional Loss SNV dbSNP153 33..33 33 - - - 73738 RMVar_ID_73738 Human_SNP_ID_326550047 m1A Human chr7 + 75712860 75712856 75712860 AGTCACTCATCCATTCATTTATATACTCCTTCATTCACTCACTCATTCATTCACTCATTCACTGA AGTCACTCATCCATTCATTTATATACTCC____TTCACTCACTCATTCATTCACTCATTCACTGA CTTCA C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75712619..75712979 26863196 MeRIP-seq:(Medium) rs1171490024 Functional Loss DEL dbSNP153 30..33 33 - - - 73739 RMVar_ID_73739 Human_SNP_ID_326556342 m1A Human chr7 - 75738920 75738920 75738920 CGAGGGCCCCTGACTCGGCTCCTCGCGGCGACATGGATCGGATGGCCAGCTCCATGAAGCAGGTG CGAGGGCCCCTGACTCGGCTCCTCGCGGCGACTTGGATCGGATGGCCAGCTCCATGAAGCAGGTG T A HIP1 Ensembl:ENSG00000127946 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75738804..75738928 26863196 MeRIP-seq:(Medium) rs1362510913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956424,Human_RBP_ID_23080081 Human_miRNA_ID_2392895,Human_miRNA_ID_2392896 73740 RMVar_ID_73740 Human_SNP_ID_326556343 m1A Human chr7 - 75738920 75738920 75738920 CGAGGGCCCCTGACTCGGCTCCTCGCGGCGACATGGATCGGATGGCCAGCTCCATGAAGCAGGTG CGAGGGCCCCTGACTCGGCTCCTCGCGGCGACGTGGATCGGATGGCCAGCTCCATGAAGCAGGTG T C HIP1 Ensembl:ENSG00000127946 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75738804..75738928 26863196 MeRIP-seq:(Medium) rs1362510913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956424,Human_RBP_ID_23080081 Human_miRNA_ID_2392895,Human_miRNA_ID_2392896 73741 RMVar_ID_73741 Human_SNP_ID_326565495 m1A Human chr7 - 75769733 75769733 75769733 AGTCTGTACCCATCCAAGGAAAAAATGGGTGCAAAAATACATTTCTTTACTGAAAACTCCGAAAC AGTCTGTACCCATCCAAGGAAAAAATGGGTGCCAAAATACATTTCTTTACTGAAAACTCCGAAAC T G CCL26 Ensembl:ENSG00000006606 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:75769673..75769768 32194978 MeRIP-seq:(Medium) rs781867529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_878684,Human_Splice_Rec_878690 73742 RMVar_ID_73742 Human_SNP_ID_326595633 m1A Human chr7 - 75879113 75879113 75879113 GGTGGCGGATGGCACCTCGGGACACAAGCACCAGCTGCGACACCCGGGCCCCGAGGCCGCCATGG GGTGGCGGATGGCACCTCGGGACACAAGCACCCGCTGCGACACCCGGGCCCCGAGGCCGCCATGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75879064..75879209 26863196 MeRIP-seq:(Medium) rs1554541938 Functional Loss SNV dbSNP153 33..33 33 - - - 73743 RMVar_ID_73743 Human_SNP_ID_326598173 m1A Human chr7 + 75888075 75888075 75888075 GTCCCCAAGCCACCCTGTGTCCCAGACGCAGCACGCCAGTGGTCAGAAGCTGGCCTCCTGGCCCT GTCCCCAAGCCACCCTGTGTCCCAGACGCAGCGCGCCAGTGGTCAGAAGCTGGCCTCCTGGCCCT A G RHBDD2 Ensembl:ENSG00000005486 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:75888026..75888125 26863196 MeRIP-seq:(Medium) rs782733037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4965049,Human_RBP_ID_17426970,Human_RBP_ID_18960137 Human_Splice_Rec_878716,Human_Splice_Rec_878724,Human_Splice_Rec_878730,Human_Splice_Rec_878736,Human_Splice_Rec_878740,Human_Splice_Rec_878742 RMVar_hsa_circ_119172,RMVar_hsa_circ_122849,RMVar_hsa_circ_245760,RMVar_hsa_circ_245761 73744 RMVar_ID_73744 Human_SNP_ID_326598198 m1A Human chr7 - 75888126 75888126 75888126 CGGAGGCAGGCTGGTACGGAGGCAAGGTGGGCATGTGCCCGGGGGTGCAGGAGGGCCAGGAGGCC CGGAGGCAGGCTGGTACGGAGGCAAGGTGGGCGTGTGCCCGGGGGTGCAGGAGGGCCAGGAGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75888077..75888180 26863196 MeRIP-seq:(Medium) rs782042422 Functional Loss SNV dbSNP153 33..33 33 - - - 73745 RMVar_ID_73745 Human_SNP_ID_326598215 m1A Human chr7 + 75888168 75888168 75888168 GCCTCCGTACCAGCCTGCCTCCGGCCTGTGCTATGTGCAGAACCACTTTGGTCCAAACCCCACCT GCCTCCGTACCAGCCTGCCTCCGGCCTGTGCTGTGTGCAGAACCACTTTGGTCCAAACCCCACCT A G RHBDD2 Ensembl:ENSG00000005486 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:75888126..75888200 26863196 MeRIP-seq:(Medium) rs1392851442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252924,Human_RBP_ID_688127,Human_RBP_ID_5429741,Human_RBP_ID_16219800,Human_RBP_ID_17092893,Human_RBP_ID_17314587,Human_RBP_ID_17542228,Human_RBP_ID_18960138,Human_RBP_ID_22774369 Human_miRNA_ID_2057632,Human_miRNA_ID_2845584,Human_miRNA_ID_2848604 RMVar_hsa_circ_119172,RMVar_hsa_circ_122849,RMVar_hsa_circ_245760,RMVar_hsa_circ_245761 73746 RMVar_ID_73746 Human_SNP_ID_326605293 m1A Human chr7 - 75915194 75915194 75915194 GGCCCGACCTCACCCACCCCGCCGTCGCCGCGAAAGATAGCACTCACCGCTGGCAGCCCGGCTGC GGCCCGACCTCACCCACCCCGCCGTCGCCGCGCAAGATAGCACTCACCGCTGGCAGCCCGGCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75915192..75915373 26863196 MeRIP-seq:(Medium) rs923301483 Functional Loss SNV dbSNP153 33..33 33 - - - 73747 RMVar_ID_73747 Human_SNP_ID_326605305 m1A Human chr7 - 75915211 75915211 75915211 CAAACCCCGAGTCTTGGGGCCCGACCTCACCCACCCCGCCGTCGCCGCGAAAGATAGCACTCACC CAAACCCCGAGTCTTGGGGCCCGACCTCACCCCCCCCGCCGTCGCCGCGAAAGATAGCACTCACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:75915206..75915390 26863196 MeRIP-seq:(Medium) rs1554547903 Functional Loss SNV dbSNP153 33..33 33 - - - 73748 RMVar_ID_73748 Human_SNP_ID_326611549 m1A Human chr7 - 75939267 75939266 75939268 GGCAGGCAGGCTCCTAATCCCACAGAGCTTACAGTCTGGAAAGCCTCTAGACAATGTTCAGGTAC GGCAGGCAGGCTCCTAATCCCACAGAGCTTA__GTCTGGAAAGCCTCTAGACAATGTTCAGGTAC CTG C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:75939260..75939389 26863196 MeRIP-seq:(Medium) rs1458224968 Functional Loss DEL dbSNP153 32..33 33 - - - 73749 RMVar_ID_73749 Human_SNP_ID_326615452 m1A Human chr7 - 75954069 75954069 75954069 TGAGCGAAAACAGAATCATGTCCGTCATGCTGAAAAGAGATACTTCTTCGGCCACCGCCTCGGAC TGAGCGAAAACAGAATCATGTCCGTCATGCTGTAAAGAGATACTTCTTCGGCCACCGCCTCGGAC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:75953960..75954109 26863196 MeRIP-seq:(Medium) rs1554553353 Functional Loss SNV dbSNP153 33..33 33 - - - 73750 RMVar_ID_73750 Human_SNP_ID_326615453 m1A Human chr7 - 75954069 75954069 75954069 TGAGCGAAAACAGAATCATGTCCGTCATGCTGAAAAGAGATACTTCTTCGGCCACCGCCTCGGAC TGAGCGAAAACAGAATCATGTCCGTCATGCTGGAAAGAGATACTTCTTCGGCCACCGCCTCGGAC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:75953960..75954109 26863196 MeRIP-seq:(Medium) rs1554553353 Functional Loss SNV dbSNP153 33..33 33 - - - 73751 RMVar_ID_73751 Human_SNP_ID_326619980 m1A Human chr7 + 75971541 75971535 75971542 GGGGTGGTGCGGGGGTAGAAGGCCAGAAGTGGACAGTGGACAGAAGATTGTGTCACCCCAGCCTG GGGGTGGTGCGGGGGTAGAAGGCCAGA_______AGTGGACAGAAGATTGTGTCACCCCAGCCTG AAGTGGAC A POR Ensembl:ENSG00000127948 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:75971538..75972143 26863196 MeRIP-seq:(Medium) rs142518547 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_3864180,Human_RBP_ID_18959328 RMVar_hsa_circ_86877,RMVar_hsa_circ_103197,RMVar_hsa_circ_309727,RMVar_hsa_circ_107617,RMVar_hsa_circ_245763,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762,RMVar_hsa_circ_245764 73752 RMVar_ID_73752 Human_SNP_ID_326620107 m1A Human chr7 - 75972015 75972015 75972015 GTCCCCACGGCCTGACCTCAGCCTGACCTTCCACCTCTTCACCTCTTCCTTCTCCAGCCCCTGCC GTCCCCACGGCCTGACCTCAGCCTGACCTTCCCCCTCTTCACCTCTTCCTTCTCCAGCCCCTGCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:75971934..75972132 26863196 MeRIP-seq:(Medium) rs1554556223 Functional Loss SNV dbSNP153 33..33 33 - - - 73753 RMVar_ID_73753 Human_SNP_ID_326622503 m1A Human chr7 - 75980305 75980305 75980305 TGCAGAAACAGGGACAGGACCGCGCCCCGGCCATGACTGAGCCTGTTCAAGGTTCAACCCGCACC TGCAGAAACAGGGACAGGACCGCGCCCCGGCCGTGACTGAGCCTGTTCAAGGTTCAACCCGCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:75980302..75980523 26863196 MeRIP-seq:(Medium) rs781819982 Functional Loss SNV dbSNP153 33..33 33 - - - 73754 RMVar_ID_73754 Human_SNP_ID_326622584 m1A Human chr7 - 75980484 75980484 75980484 AGCCCATAGCAGTCTCTGGGTGACTCACCGCGAACTTGACCCCAGAGAGATCCACGTCTGTCTCC AGCCCATAGCAGTCTCTGGGTGACTCACCGCGGACTTGACCCCAGAGAGATCCACGTCTGTCTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:75980437..75980537 32194978 MeRIP-seq:(Medium) rs1554557575 Functional Loss SNV dbSNP153 33..33 33 - - - 73755 RMVar_ID_73755 Human_SNP_ID_326622889 m1A Human chr7 + 75981163 75981157 75981163 CCAGCGCATCTTTGAGCTGGGGTTGGGCGACGACGATGGGAAGTGAGTGCCCACCCTGCCACCAT CCAGCGCATCTTTGAGCTGGGGTTGGG______CGATGGGAAGTGAGTGCCCACCCTGCCACCAT GCGACGA G POR Ensembl:ENSG00000127948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:75981049..75981171 26863196 MeRIP-seq:(Medium) rs782715212 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_843409,Human_RBP_ID_952549,Human_RBP_ID_5123019,Human_RBP_ID_9311323,Human_RBP_ID_22110876,Human_RBP_ID_22463139,Human_RBP_ID_22774931,Human_RBP_ID_26357850 Human_Splice_Rec_878779,Human_Splice_Rec_878817,Human_Splice_Rec_878917,Human_Splice_Rec_878955 RMVar_hsa_circ_103197,RMVar_hsa_circ_107617,RMVar_hsa_circ_245763,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762 73756 RMVar_ID_73756 Human_SNP_ID_326623330 m1A Human chr7 + 75982279 75982279 75982279 TCCACACCGACATAGATGCGGCCAAGGTGTACATGGGGGAGATGGGCCGGCTGAAGAGCTACGAG TCCACACCGACATAGATGCGGCCAAGGTGTACGTGGGGGAGATGGGCCGGCTGAAGAGCTACGAG A G POR Ensembl:ENSG00000127948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr7:75982195..75982352;chr7:75982073..75983334 26863196,32194978 MeRIP-seq:(Medium) rs781900160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14430,Human_RBP_ID_253347,Human_RBP_ID_953697,Human_RBP_ID_3972068,Human_RBP_ID_22464045,Human_RBP_ID_22774377 Human_Splice_Rec_878782,Human_Splice_Rec_878783,Human_Splice_Rec_878820,Human_Splice_Rec_878821,Human_Splice_Rec_878876,Human_Splice_Rec_878877,Human_Splice_Rec_878894,Human_Splice_Rec_878895,Human_Splice_Rec_878920,Human_Splice_Rec_878921,Human_Splice_Rec_878958,Human_Splice_Rec_878959,Human_Splice_Rec_878964,Human_Splice_Rec_878965 RMVar_hsa_circ_15390,RMVar_hsa_circ_103197,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762 73757 RMVar_ID_73757 Human_SNP_ID_326623903 m1A Human chr7 - 75983830 75983827 75983830 ACTCACCATCCAGGTTGTTCAGGGACATGACGACGTCCAGGTCGGCACCCAGGATTTTGCCCAGC ACTCACCATCCAGGTTGTTCAGGGACATGACG___TCCAGGTCGGCACCCAGGATTTTGCCCAGC ACGT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:75983780..75984800 32194978 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 33..35 33 - - - Human_RBP_ID_16220621 73758 RMVar_ID_73758 Human_SNP_ID_326624288 m1A Human chr7 + 75984854 75984854 75984854 GCACGGCCCTCACCTACTACCTGGACATCACCAACCCGCCGCGTACCAACGTGCTGTACGAGCTG GCACGGCCCTCACCTACTACCTGGACATCACCGACCCGCCGCGTACCAACGTGCTGTACGAGCTG A G POR Ensembl:ENSG00000127948 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75984745..75984989 26863196 MeRIP-seq:(Medium) rs575786687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955806,Human_RBP_ID_5123020,Human_RBP_ID_22463572,Human_RBP_ID_22774637,Human_RBP_ID_27533613 Human_Splice_Rec_878788,Human_Splice_Rec_878826,Human_Splice_Rec_878900,Human_Splice_Rec_878926,Human_Splice_Rec_878970,Human_Splice_Rec_878984,Human_Splice_Rec_878990,Human_Splice_Rec_878994 RMVar_hsa_circ_103197,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762,RMVar_hsa_circ_40421,RMVar_hsa_circ_75971,RMVar_hsa_circ_86094,RMVar_hsa_circ_245767,RMVar_hsa_circ_245768 73759 RMVar_ID_73759 Human_SNP_ID_326627098 m1A Human chr7 - 75990180 75990180 75990180 GTGGAGAGGCGAGTGCTGGGAACCAGATGGCGAGCTGAGTGGGGACACATCCGCAGCCTGGTGGG GTGGAGAGGCGAGTGCTGGGAACCAGATGGCGTGCTGAGTGGGGACACATCCGCAGCCTGGTGGG T A TMEM120A Ensembl:ENSG00000189077 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:75990136..75990420 26863196 MeRIP-seq:(Medium) rs1563443037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9439756 RMVar_hsa_circ_77049,RMVar_hsa_circ_245775 73760 RMVar_ID_73760 Human_SNP_ID_326627393 m1A Human chr7 + 75991215 75991215 75991215 CGTCCTCCTGGGTGACAGCTGCTGGCCTTTCCAGGTGCACATTCCACCGCCCCCGCCCGCCTACT CGTCCTCCTGGGTGACAGCTGCTGGCCTTTCCGGGTGCACATTCCACCGCCCCCGCCCGCCTACT A G RF00017-4706,RF00017-4541 RNACentral:URS0000954994,RNACentral:URS0000992647 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:75991109..75991367 26863196 MeRIP-seq:(Medium) rs150564443 Functional Loss SNV dbSNP153 33..33 33 - - - 73761 RMVar_ID_73761 Human_SNP_ID_326639308 m1A Human chr7 + 76033623 76033623 76033623 CTGGGAAATGCCAGCACCTCAACTTAAACCTCAGATCCTTCTCACCTCCTCAAAGACTTCAGTTC CTGGGAAATGCCAGCACCTCAACTTAAACCTCGGATCCTTCTCACCTCCTCAAAGACTTCAGTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76033620..76033743 26863196 MeRIP-seq:(Medium) rs1301599370 Functional Loss SNV dbSNP153 33..33 33 - - - 73762 RMVar_ID_73762 Human_SNP_ID_326639312 m1A Human chr7 + 76033643 76033641 76033643 AACTTAAACCTCAGATCCTTCTCACCTCCTCAAAGACTTCAGTTCTCAGCACCCCCTCCACAGCA AACTTAAACCTCAGATCCTTCTCACCTCCTC__AGACTTCAGTTCTCAGCACCCCCTCCACAGCA CAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76033593..76033721 26863196 MeRIP-seq:(Medium) rs1427913451 Functional Loss DEL dbSNP153 32..33 33 - - - 73763 RMVar_ID_73763 Human_SNP_ID_326642111 m1A Human chr7 + 76045113 76045113 76045113 ATAACCTCCTTTATTTTTCTCCTCTCCTTTGTATAACCCGACTTCCCTCTTTATGTATTTTCCAC ATAACCTCCTTTATTTTTCTCCTCTCCTTTGTGTAACCCGACTTCCCTCTTTATGTATTTTCCAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76045025..76045230 26863196 MeRIP-seq:(Medium) rs782749896 Functional Loss SNV dbSNP153 33..33 33 - - - 73764 RMVar_ID_73764 Human_SNP_ID_326643215 m1A Human chr7 - 76048193 76048193 76048193 TGGGCCGAGGTGCTGAAGCTGCGGCGGAGAGCAGCGCTGGCAGGCCGGGCGAGGGCGGAGAGCAT TGGGCCGAGGTGCTGAAGCTGCGGCGGAGAGCGGCGCTGGCAGGCCGGGCGAGGGCGGAGAGCAT T C lnc-STYXL1-1 RNACentral:URS00008B5DFD lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,untreat control chr7:76048076..76048308;chr7:76048101..76048300;chr7:76048100..76048288;chr7:76048105..76048204 26863196,26863410 MeRIP-seq:(Medium) rs1554584467 Functional Loss SNV dbSNP153 33..33 33 - - - 73765 RMVar_ID_73765 Human_SNP_ID_326643218 m1A Human chr7 - 76048196 76048196 76048196 ACCTGGGCCGAGGTGCTGAAGCTGCGGCGGAGAGCAGCGCTGGCAGGCCGGGCGAGGGCGGAGAG ACCTGGGCCGAGGTGCTGAAGCTGCGGCGGAGGGCAGCGCTGGCAGGCCGGGCGAGGGCGGAGAG T C lnc-STYXL1-1 RNACentral:URS00008B5DFD lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chr7:76048051..76048287;chr7:76048100..76048201 26863410 MeRIP-seq:(Medium) rs1202158789 Functional Loss SNV dbSNP153 33..33 33 - - - 73766 RMVar_ID_73766 Human_SNP_ID_326643233 m1A Human chr7 - 76048218 76048218 76048218 CAGGCCGCCCCTCGTCTGGCCTACCTGGGCCGAGGTGCTGAAGCTGCGGCGGAGAGCAGCGCTGG CAGGCCGCCCCTCGTCTGGCCTACCTGGGCCGCGGTGCTGAAGCTGCGGCGGAGAGCAGCGCTGG T G lnc-STYXL1-1 RNACentral:URS00008B5DFD lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:76048150..76048250 32194978 MeRIP-seq:(Medium) rs782450987 Functional Loss SNV dbSNP153 33..33 33 - - - 73767 RMVar_ID_73767 Human_SNP_ID_326643679 m1A Human chr7 + 76049452 76049452 76049452 AAGTGAGAAGTGACACTTGATATGGGACAGGAATGAGTAAACTTAGGACAGGTGGAAGCGATGAA AAGTGAGAAGTGACACTTGATATGGGACAGGACTGAGTAAACTTAGGACAGGTGGAAGCGATGAA A C MDH2 Ensembl:ENSG00000146701 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76049449..76049540 26863196 MeRIP-seq:(Medium) rs994653639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16221141 RMVar_hsa_circ_123878,RMVar_hsa_circ_245800 73768 RMVar_ID_73768 Human_SNP_ID_326645069 m1A Human chr7 + 76054896 76054896 76054896 GAGGCATCGGGCAGCCACTTTCACTTCTCCTGAAGAACAGCCCCTTGGTGAGCCGCCTGACCCTC GAGGCATCGGGCAGCCACTTTCACTTCTCCTGCAGAACAGCCCCTTGGTGAGCCGCCTGACCCTC A C MDH2 Ensembl:ENSG00000146701 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:76054851..76054925;chr7:76054851..76054900;chr7:76054826..76054975 26863196 MeRIP-seq:(Medium) rs1554585969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688195,Human_RBP_ID_4965083,Human_RBP_ID_9213045,Human_RBP_ID_18195968,Human_RBP_ID_18885782,Human_RBP_ID_22325651,Human_RBP_ID_22464062,Human_RBP_ID_27116673,Human_RBP_ID_27533625 Human_Splice_Rec_879316,Human_Splice_Rec_879332,Human_Splice_Rec_879338,Human_Splice_Rec_879342 RMVar_hsa_circ_74852,RMVar_hsa_circ_123878,RMVar_hsa_circ_245800,RMVar_hsa_circ_106348,RMVar_hsa_circ_303114,RMVar_hsa_circ_245801,RMVar_hsa_circ_49156,RMVar_hsa_circ_245802 73769 RMVar_ID_73769 Human_SNP_ID_326645726 m1A Human chr7 - 76057456 76057456 76057456 TTTCTGGGGACTCCAGCCGGAATAACTACCACATCACAACCTTTCAGGCAGTCAGGCAGCTGTTC TTTCTGGGGACTCCAGCCGGAATAACTACCACTTCACAACCTTTCAGGCAGTCAGGCAGCTGTTC T A lnc-STYXL1-1 RNACentral:URS00008B5DFD lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:76057401..76057500 26863196 MeRIP-seq:(Medium) rs1360053717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2700610,Human_miRNA_ID_2700611,Human_miRNA_ID_2719813,Human_miRNA_ID_2719814 73770 RMVar_ID_73770 Human_SNP_ID_326647539 m1A Human chr7 + 76064342 76064342 76064342 ACTCACTGATCCCATGGCTTGGCTTGCAGTGCACCCCCAAGGTGGACTTTCCCCAGGACCAGCTG ACTCACTGATCCCATGGCTTGGCTTGCAGTGCGCCCCCAAGGTGGACTTTCCCCAGGACCAGCTG A G MDH2 Ensembl:ENSG00000146701 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782104893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688212,Human_RBP_ID_953703,Human_RBP_ID_1052918,Human_RBP_ID_1688778,Human_RBP_ID_9337201,Human_RBP_ID_17665034,Human_RBP_ID_22463149,Human_RBP_ID_22774384,Human_RBP_ID_27116685,Human_RBP_ID_27359973 Human_Splice_Rec_879310,Human_Splice_Rec_879311,Human_Splice_Rec_879326,Human_Splice_Rec_879327,Human_Splice_Rec_879350,Human_Splice_Rec_879351,Human_Splice_Rec_879360,Human_Splice_Rec_879361 RMVar_hsa_circ_74852,RMVar_hsa_circ_123878,RMVar_hsa_circ_245800,RMVar_hsa_circ_6588,RMVar_hsa_circ_95044,RMVar_hsa_circ_85598,RMVar_hsa_circ_245803,RMVar_hsa_circ_108931,RMVar_hsa_circ_245807,RMVar_hsa_circ_124910,RMVar_hsa_circ_245810,RMVar_hsa_circ_245811 73771 RMVar_ID_73771 Human_SNP_ID_326647567 m1A Human chr7 + 76064400 76064400 76064400 CCAGCTGACAGCACTCACTGGGCGGATCCAGGAGGCCGGCACGGAGGTGGTCAAGGCTAAAGCCG CCAGCTGACAGCACTCACTGGGCGGATCCAGGCGGCCGGCACGGAGGTGGTCAAGGCTAAAGCCG A C MDH2 Ensembl:ENSG00000146701 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:76064294..76064483 26863196 MeRIP-seq:(Medium) rs782672155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253526,Human_RBP_ID_793589,Human_RBP_ID_953703,Human_RBP_ID_7758227,Human_RBP_ID_8671448,Human_RBP_ID_9213046,Human_RBP_ID_9337829,Human_RBP_ID_18104092,Human_RBP_ID_22463150,Human_RBP_ID_22534254,Human_RBP_ID_22774950,Human_RBP_ID_22835517,Human_RBP_ID_27116685,Human_RBP_ID_27359973 Human_Splice_Rec_879310,Human_Splice_Rec_879311,Human_Splice_Rec_879326,Human_Splice_Rec_879327,Human_Splice_Rec_879350,Human_Splice_Rec_879351,Human_Splice_Rec_879360,Human_Splice_Rec_879361 Human_miRNA_ID_2015590,Human_miRNA_ID_2464785 RMVar_hsa_circ_74852,RMVar_hsa_circ_123878,RMVar_hsa_circ_245800,RMVar_hsa_circ_6588,RMVar_hsa_circ_95044,RMVar_hsa_circ_85598,RMVar_hsa_circ_245803,RMVar_hsa_circ_108931,RMVar_hsa_circ_245807,RMVar_hsa_circ_124910,RMVar_hsa_circ_245810,RMVar_hsa_circ_245811 73772 RMVar_ID_73772 Human_SNP_ID_326647784 m1A Human chr7 - 76064933 76064931 76064934 CTGGATACGTACCCCAAGCAGCAGCGGTGTGGAGAAGTAGGTACATTCCGTTTCCTGTGACTTAA CTGGATACGTACCCCAAGCAGCAGCGGTGTG___AAGTAGGTACATTCCGTTTCCTGTGACTTAA TCTC T lnc-STYXL1-1 RNACentral:URS00008B5DFD lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:76064784..76064984 26863196 MeRIP-seq:(Medium) rs782344021 Functional Loss DEL dbSNP153 32..34 33 - - - 73773 RMVar_ID_73773 Human_SNP_ID_326701781 m1A Human chr7 - 76281125 76281123 76281125 AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAGAGGAAGAGAGAAAAAGAGCAGGAGAGAGACAGA AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAG__GAAGAGAGAAAAAGAGCAGGAGAGAGACAGA CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76281057..76281390 26863196 MeRIP-seq:(Medium) rs1374401830 Functional Loss DEL dbSNP153 33..34 33 - - - 73774 RMVar_ID_73774 Human_SNP_ID_326701782 m1A Human chr7 - 76281125 76281125 76281125 AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAGAGGAAGAGAGAAAAAGAGCAGGAGAGAGACAGA AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAGGGGAAGAGAGAAAAAGAGCAGGAGAGAGACAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76281057..76281390 26863196 MeRIP-seq:(Medium) rs1171379082 Functional Loss SNV dbSNP153 33..33 33 - - - 73775 RMVar_ID_73775 Human_SNP_ID_326701783 m1A Human chr7 - 76281125 76281125 76281125 AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAGAGGAAGAGAGAAAAAGAGCAGGAGAGAGACAGA AGGGAGAGAGGGAGGAGGCAGAGAAGAGAAAGCGGAAGAGAGAAAAAGAGCAGGAGAGAGACAGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76281057..76281390 26863196 MeRIP-seq:(Medium) rs1171379082 Functional Loss SNV dbSNP153 33..33 33 - - - 73776 RMVar_ID_73776 Human_SNP_ID_326703313 m1A Human chr7 + 76286014 76286014 76286014 GGGACCGGGGAAGACTTTGAGGGTGGGCATCCAGTGGACAAGGAGAAGCCAGATGTGCTGCTTCT GGGACCGGGGAAGACTTTGAGGGTGGGCATCCTGTGGACAAGGAGAAGCCAGATGTGCTGCTTCT A T SRRM3 Ensembl:ENSG00000177679 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76286004..76286089 26863196 MeRIP-seq:(Medium) rs1388240869 Functional Loss SNV dbSNP153 33..33 33 - - - 73777 RMVar_ID_73777 Human_SNP_ID_326708144 m1A Human chr7 + 76302695 76302695 76302695 CCAGCGCCCCGCACTTTTCTGAGCAGACGTCCAGAGCAGAGTCAGCCAGCATGACCGAGCGCCGC CCAGCGCCCCGCACTTTTCTGAGCAGACGTCCGGAGCAGAGTCAGCCAGCATGACCGAGCGCCGC A G HSPB1 Ensembl:ENSG00000106211 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:76302576..76303125 26863196 MeRIP-seq:(Medium) rs1403880807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688254,Human_RBP_ID_843816,Human_RBP_ID_4956438,Human_RBP_ID_5327888 Human_miRNA_ID_2331252,Human_miRNA_ID_2453792,Human_miRNA_ID_2907177,Human_miRNA_ID_2964334,Human_miRNA_ID_3026013 RMVar_hsa_circ_122330,RMVar_hsa_circ_245816 73778 RMVar_ID_73778 Human_SNP_ID_326708188 m1A Human chr7 - 76302741 76302741 76302741 CGCGGAAGGGGTCCCAGCTGGGGCCCCGCAGGAGCGAGAAGGGGACGCGGCGCTCGGTCATGCTG CGCGGAAGGGGTCCCAGCTGGGGCCCCGCAGGTGCGAGAAGGGGACGCGGCGCTCGGTCATGCTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76302626..76303000 26863196 MeRIP-seq:(Medium) rs772216758 Functional Loss SNV dbSNP153 33..33 33 - - - 73779 RMVar_ID_73779 Human_SNP_ID_326708418 m1A Human chr7 + 76303073 76303073 76303073 CGGTCAAGACCAAGGATGGCGTGGTGGAGATCACCGGTGAGCCCCCCTGCTCCTGCAGGGGAGAG CGGTCAAGACCAAGGATGGCGTGGTGGAGATCTCCGGTGAGCCCCCCTGCTCCTGCAGGGGAGAG A T HSPB1 Ensembl:ENSG00000106211 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76302576..76303108 26863196 MeRIP-seq:(Medium) rs17850893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19136638,Human_RBP_ID_22463159 Human_Splice_Rec_879427 RMVar_hsa_circ_122330,RMVar_hsa_circ_245816 73780 RMVar_ID_73780 Human_SNP_ID_326708748 m1A Human chr7 - 76303626 76303626 76303626 GCCCGCCGGTCTGGGCTCTCAGAAACTTCCGGAAAGTTCTTCGATTCAGAGTTTTGGGAGGAACG GCCCGCCGGTCTGGGCTCTCAGAAACTTCCGGGAAGTTCTTCGATTCAGAGTTTTGGGAGGAACG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76303625..76304030 26863196 MeRIP-seq:(Medium) rs1314262384 Functional Loss SNV dbSNP153 33..33 33 - - - 73781 RMVar_ID_73781 Human_SNP_ID_326708836 m1A Human chr7 - 76303777 76303777 76303777 GTGCTTGCCTTTGGGGGGAAGAGGGAAATCAGACTGCGGGGGAGGGGACTGCCTTTCGGCCCCGC GTGCTTGCCTTTGGGGGGAAGAGGGAAATCAGGCTGCGGGGGAGGGGACTGCCTTTCGGCCCCGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76303776..76303800 26863196 MeRIP-seq:(Medium) rs773073334 Functional Loss SNV dbSNP153 33..33 33 - - - 73782 RMVar_ID_73782 Human_SNP_ID_326708889 m1A Human chr7 + 76303829 76303829 76303829 CAAAGGCAAGCACGAGGAGCGGCAGGACGAGCATGGCTACATCTCCCGGTGCTTCACGCGGAAAT CAAAGGCAAGCACGAGGAGCGGCAGGACGAGCGTGGCTACATCTCCCGGTGCTTCACGCGGAAAT A G HSPB1 Ensembl:ENSG00000106211 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:76303731..76303998 26863410 MeRIP-seq:(Medium) rs1554614638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688262,Human_RBP_ID_5123270 Human_Splice_Rec_879428,Human_Splice_Rec_879429,Human_Splice_Rec_879431,Human_Splice_Rec_879434,Human_Splice_Rec_879435 Human_miRNA_ID_3011447 RMVar_hsa_circ_122330,RMVar_hsa_circ_78742,RMVar_hsa_circ_126746,RMVar_hsa_circ_245816,RMVar_hsa_circ_245817,RMVar_hsa_circ_245818 73783 RMVar_ID_73783 Human_SNP_ID_326708890 m1A Human chr7 - 76303830 76303830 76303830 TATTTCCGCGTGAAGCACCGGGAGATGTAGCCATGCTCGTCCTGCCGCTCCTCGTGCTTGCCTTT TATTTCCGCGTGAAGCACCGGGAGATGTAGCCGTGCTCGTCCTGCCGCTCCTCGTGCTTGCCTTT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:76303731..76303998 26863410 MeRIP-seq:(Medium) rs763861274 Functional Loss SNV dbSNP153 33..33 33 - - - 73784 RMVar_ID_73784 Human_SNP_ID_326708915 m1A Human chr7 + 76303858 76303858 76303858 AGCATGGCTACATCTCCCGGTGCTTCACGCGGAAATACACGTGAGTCCTGGCGCCAGGTCGGGGT AGCATGGCTACATCTCCCGGTGCTTCACGCGGCAATACACGTGAGTCCTGGCGCCAGGTCGGGGT A C HSPB1 Ensembl:ENSG00000106211 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76303629..76303875 26863196 MeRIP-seq:(Medium) rs1554614650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688262 Human_Splice_Rec_879428,Human_Splice_Rec_879429,Human_Splice_Rec_879431,Human_Splice_Rec_879434,Human_Splice_Rec_879435 RMVar_hsa_circ_122330,RMVar_hsa_circ_78742,RMVar_hsa_circ_126746,RMVar_hsa_circ_245816,RMVar_hsa_circ_245817,RMVar_hsa_circ_245818 73785 RMVar_ID_73785 Human_SNP_ID_326709019 m1A Human chr7 - 76303986 76303986 76303986 AGGAAACTTGGGTGGGGTCCACACCGGGGGGCAGCCTGGACGTGCAGAGAGGAAAGGCAAGCGTT AGGAAACTTGGGTGGGGTCCACACCGGGGGGCGGCCTGGACGTGCAGAGAGGAAAGGCAAGCGTT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76303976..76304000 26863196 MeRIP-seq:(Medium) rs768587418 Functional Loss SNV dbSNP153 33..33 33 - - - 73786 RMVar_ID_73786 Human_SNP_ID_326709134 m1A Human chr7 + 76304157 76304157 76304157 GCTTGGGGGCCCAGAAGCTGCAAAATCCGATGAGACTGCCGCCAAGTAAAGCCTTAGCCCGGATG GCTTGGGGGCCCAGAAGCTGCAAAATCCGATGGGACTGCCGCCAAGTAAAGCCTTAGCCCGGATG A G HSPB1 Ensembl:ENSG00000106211 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76304126..76304225;chr7:76304112..76304300 26863196 MeRIP-seq:(Medium) rs374801083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688264,Human_RBP_ID_956551,Human_RBP_ID_17092896,Human_RBP_ID_17664556,Human_RBP_ID_21397241,Human_RBP_ID_22534326,Human_RBP_ID_24226657 RMVar_hsa_circ_122330,RMVar_hsa_circ_78742,RMVar_hsa_circ_126746,RMVar_hsa_circ_245816,RMVar_hsa_circ_245817,RMVar_hsa_circ_123977,RMVar_hsa_circ_245818,RMVar_hsa_circ_245819 73787 RMVar_ID_73787 Human_SNP_ID_326709135 m1A Human chr7 + 76304157 76304157 76304157 GCTTGGGGGCCCAGAAGCTGCAAAATCCGATGAGACTGCCGCCAAGTAAAGCCTTAGCCCGGATG GCTTGGGGGCCCAGAAGCTGCAAAATCCGATGTGACTGCCGCCAAGTAAAGCCTTAGCCCGGATG A T HSPB1 Ensembl:ENSG00000106211 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76304126..76304225;chr7:76304112..76304300 26863196 MeRIP-seq:(Medium) rs374801083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688264,Human_RBP_ID_956551,Human_RBP_ID_17092896,Human_RBP_ID_17664556,Human_RBP_ID_21397241,Human_RBP_ID_22534326,Human_RBP_ID_24226657 RMVar_hsa_circ_122330,RMVar_hsa_circ_78742,RMVar_hsa_circ_126746,RMVar_hsa_circ_245816,RMVar_hsa_circ_245817,RMVar_hsa_circ_123977,RMVar_hsa_circ_245818,RMVar_hsa_circ_245819 73788 RMVar_ID_73788 Human_SNP_ID_326709164 m1A Human chr7 + 76304193 76304193 76304193 TGCCGCCAAGTAAAGCCTTAGCCCGGATGCCCACCCCTGCTGCCGCCACTGGCTGTGCCTCCCCC TGCCGCCAAGTAAAGCCTTAGCCCGGATGCCCCCCCCTGCTGCCGCCACTGGCTGTGCCTCCCCC A C HSPB1 Ensembl:ENSG00000106211 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:76304146..76304246 32194978 MeRIP-seq:(Medium) rs775953415 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_253167,Human_RBP_ID_688268,Human_RBP_ID_793039,Human_RBP_ID_843817,Human_RBP_ID_5123272,Human_RBP_ID_17092896,Human_RBP_ID_17665043,Human_RBP_ID_22534326 Human_miRNA_ID_1705877,Human_miRNA_ID_2221031,Human_miRNA_ID_2484078,Human_miRNA_ID_2873099,Human_miRNA_ID_2981062,Human_miRNA_ID_3072455 RMVar_hsa_circ_122330,RMVar_hsa_circ_78742,RMVar_hsa_circ_126746,RMVar_hsa_circ_245816,RMVar_hsa_circ_245817,RMVar_hsa_circ_123977,RMVar_hsa_circ_245818,RMVar_hsa_circ_245819 73789 RMVar_ID_73789 Human_SNP_ID_326716913 m1A Human chr7 + 76328531 76328531 76328531 ATTTTCACACACTGCACCACAGACCTTCTCCAAACGCCTCTCCGACCCCACAGCTTCTGCACCCA ATTTTCACACACTGCACCACAGACCTTCTCCACACGCCTCTCCGACCCCACAGCTTCTGCACCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:76328481..76328566 26863196 MeRIP-seq:(Medium) rs182897753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245822 73790 RMVar_ID_73790 Human_SNP_ID_326717183 m1A Human chr7 + 76329537 76329537 76329537 CCCCCAACTCATGGGAAAAAAATAAAGACTGCAGTAGTAGCATCCGCGTGCGCTGCCAGTTCCCC CCCCCAACTCATGGGAAAAAAATAAAGACTGCGGTAGTAGCATCCGCGTGCGCTGCCAGTTCCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:76329326..76329697 26863196 MeRIP-seq:(Medium) rs1003223560 Functional Loss SNV dbSNP153 33..33 33 - - - 73791 RMVar_ID_73791 Human_SNP_ID_326717195 m1A Human chr7 - 76329570 76329570 76329570 ACGATGGCGGCGAAGGCAACAATTAAGGCCCCAGGGGAACTGGCAGCGCACGCGGATGCTACTAC ACGATGGCGGCGAAGGCAACAATTAAGGCCCCGGGGGAACTGGCAGCGCACGCGGATGCTACTAC T C YWHAG Ensembl:ENSG00000170027 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76329351..76329750 26863196 MeRIP-seq:(Medium) rs745551920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1052956,Human_RBP_ID_4949429,Human_RBP_ID_7758416,Human_RBP_ID_9404593,Human_RBP_ID_16221649,Human_RBP_ID_18104157,Human_RBP_ID_22110880,Human_RBP_ID_22463161 Human_miRNA_ID_2436412,Human_miRNA_ID_2436413,Human_miRNA_ID_2436414 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821,RMVar_hsa_circ_87415,RMVar_hsa_circ_245820,RMVar_hsa_circ_245826 73792 RMVar_ID_73792 Human_SNP_ID_326717304 m1A Human chr7 - 76329901 76329901 76329901 TACTACCGCTACCTGGCTGAAGTGGCCACCGGAGAGAAAAGGGCGACGGTGGTGGAGTCCTCCGA TACTACCGCTACCTGGCTGAAGTGGCCACCGGCGAGAAAAGGGCGACGGTGGTGGAGTCCTCCGA T G YWHAG Ensembl:ENSG00000170027 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:76329851..76329925 32194978 MeRIP-seq:(Medium) rs756410758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9213111,Human_RBP_ID_9337834,Human_RBP_ID_22110882,Human_RBP_ID_22835536,Human_RBP_ID_26356599,Human_RBP_ID_27360038 Human_miRNA_ID_1967737,Human_miRNA_ID_1967738,Human_miRNA_ID_1967739 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821,RMVar_hsa_circ_87415,RMVar_hsa_circ_245820 73793 RMVar_ID_73793 Human_SNP_ID_326717349 m1A Human chr7 + 76330084 76330084 76330084 TCTATCTTCTCCCGGTACGCACGGACCATCTCAATCTTCTTCTCATTGCCGTCTGCAGATGTCTT TCTATCTTCTCCCGGTACGCACGGACCATCTCCATCTTCTTCTCATTGCCGTCTGCAGATGTCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76329501..76330250 26863196 MeRIP-seq:(Medium) rs1161419188 Functional Loss SNV dbSNP153 33..33 33 - - - 73794 RMVar_ID_73794 Human_SNP_ID_326721745 m1A Human chr7 - 76346874 76346874 76346874 TTTTGAGGGAGTAGCAGGAAATGAGTTGAAAGAGGTTAACAGGAAACAGTTCACGAAGGGCCTTC TTTTGAGGGAGTAGCAGGAAATGAGTTGAAAGGGGTTAACAGGAAACAGTTCACGAAGGGCCTTC T C YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76346872..76347137 26863196 MeRIP-seq:(Medium) rs1052885903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17167980 Human_miRNA_ID_2647589,Human_miRNA_ID_2647590,Human_miRNA_ID_2670186,Human_miRNA_ID_2670187,Human_miRNA_ID_3100836,Human_miRNA_ID_3100837 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 73795 RMVar_ID_73795 Human_SNP_ID_326725101 m1A Human chr7 - 76358849 76358849 76358849 AGTCGCGCCCTCCAAGCCCTTCAGGCCGCCCCAGTGTCCTCCTCCTTCTCCGGCCAGACCCAGCC AGTCGCGCCCTCCAAGCCCTTCAGGCCGCCCCGGTGTCCTCCTCCTTCTCCGGCCAGACCCAGCC T C YWHAG Ensembl:ENSG00000170027 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76358801..76359000 26863196 MeRIP-seq:(Medium) rs758194783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85563,Human_RBP_ID_793914,Human_RBP_ID_4955835,Human_RBP_ID_5429747,Human_RBP_ID_5452640,Human_RBP_ID_5479834,Human_RBP_ID_5513684,Human_RBP_ID_8671553,Human_RBP_ID_9337207,Human_RBP_ID_9403518,Human_RBP_ID_16222280,Human_RBP_ID_22110067,Human_RBP_ID_24517294,Human_RBP_ID_26356011,Human_RBP_ID_27360045,Human_RBP_ID_27830414 Human_miRNA_ID_1958758,Human_miRNA_ID_1958759,Human_miRNA_ID_1958760,Human_miRNA_ID_2386669,Human_miRNA_ID_2386670,Human_miRNA_ID_2386671,Human_miRNA_ID_2388143,Human_miRNA_ID_2388144,Human_miRNA_ID_2388145,Human_miRNA_ID_2399296,Human_miRNA_ID_2399297,Human_miRNA_ID_2399298,Human_miRNA_ID_3030346,Human_miRNA_ID_3030347,Human_miRNA_ID_3030348 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 73796 RMVar_ID_73796 Human_SNP_ID_326725102 m1A Human chr7 - 76358849 76358849 76358849 AGTCGCGCCCTCCAAGCCCTTCAGGCCGCCCCAGTGTCCTCCTCCTTCTCCGGCCAGACCCAGCC AGTCGCGCCCTCCAAGCCCTTCAGGCCGCCCCCGTGTCCTCCTCCTTCTCCGGCCAGACCCAGCC T G YWHAG Ensembl:ENSG00000170027 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76358801..76359000 26863196 MeRIP-seq:(Medium) rs758194783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85563,Human_RBP_ID_793914,Human_RBP_ID_4955835,Human_RBP_ID_5429747,Human_RBP_ID_5452640,Human_RBP_ID_5479834,Human_RBP_ID_5513684,Human_RBP_ID_8671553,Human_RBP_ID_9337207,Human_RBP_ID_9403518,Human_RBP_ID_16222280,Human_RBP_ID_22110067,Human_RBP_ID_24517294,Human_RBP_ID_26356011,Human_RBP_ID_27360045,Human_RBP_ID_27830414 Human_miRNA_ID_1958758,Human_miRNA_ID_1958759,Human_miRNA_ID_1958760,Human_miRNA_ID_2386669,Human_miRNA_ID_2386670,Human_miRNA_ID_2386671,Human_miRNA_ID_2388143,Human_miRNA_ID_2388144,Human_miRNA_ID_2388145,Human_miRNA_ID_2399296,Human_miRNA_ID_2399297,Human_miRNA_ID_2399298,Human_miRNA_ID_3030346,Human_miRNA_ID_3030347,Human_miRNA_ID_3030348 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 73797 RMVar_ID_73797 Human_SNP_ID_326725138 m1A Human chr7 - 76358937 76358937 76358937 CGCGGTCGCAGCTCCAGCCGCCTCCTCCGCGCAGCCGCCGCCTCAGCTGCTCGCTCTGTGGGTCG CGCGGTCGCAGCTCCAGCCGCCTCCTCCGCGCGGCCGCCGCCTCAGCTGCTCGCTCTGTGGGTCG T C YWHAG Ensembl:ENSG00000170027 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:76358776..76359000;chr7:76358671..76359000;chr7:76358667..76359000 26863196 MeRIP-seq:(Medium) rs950532550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253748,Human_RBP_ID_4955835,Human_RBP_ID_5327889,Human_RBP_ID_8912624,Human_RBP_ID_9337207,Human_RBP_ID_22534328,Human_RBP_ID_22620528 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 73798 RMVar_ID_73798 Human_SNP_ID_326738709 m1A Human chr7 - 76408632 76408632 76408632 TCACCTGGGATTTGAAATCTGTGGGGATCAGGATCGGGGGTCCTTCTCCCTCACGCCTGGGCTGA TCACCTGGGATTTGAAATCTGTGGGGATCAGGGTCGGGGGTCCTTCTCCCTCACGCCTGGGCTGA T C SSC4D Ensembl:ENSG00000146700 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76408621..76408688 26863196 MeRIP-seq:(Medium) rs917595793 Functional Loss SNV dbSNP153 33..33 33 - - - 73799 RMVar_ID_73799 Human_SNP_ID_326760593 m1A Human chr7 - 76482916 76482916 76482916 CAGAAGCGGTCCTGTGTGGGGGGTGCTGGGGGACGGGGTATGCAGGGAGGTTGGTCATGGAGTGG CAGAAGCGGTCCTGTGTGGGGGGTGCTGGGGGGCGGGGTATGCAGGGAGGTTGGTCATGGAGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76482868..76483035 26863196 MeRIP-seq:(Medium) rs2270253 Functional Loss SNV dbSNP153 33..33 33 - - - 73800 RMVar_ID_73800 Human_SNP_ID_326760602 m1A Human chr7 + 76482925 76482925 76482925 GACCAACCTCCCTGCATACCCCGTCCCCCAGCACCCCCCACACAGGACCGCTTCTGTGTTTGGGA GACCAACCTCCCTGCATACCCCGTCCCCCAGCTCCCCCCACACAGGACCGCTTCTGTGTTTGGGA A T DTX2 Ensembl:ENSG00000091073 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76482875..76482970 26863196 MeRIP-seq:(Medium) rs1286289160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83191,Human_RBP_ID_792887,Human_RBP_ID_22112593 Human_miRNA_ID_2075764,Human_miRNA_ID_2684029 RMVar_hsa_circ_352406,RMVar_hsa_circ_245844 73801 RMVar_ID_73801 Human_SNP_ID_326775725 m1A Human chr7 - 76549387 76549387 76549387 AGACTCGGTGATTCTCGTCCACTAGAGGCCAAAGCCTGGGAACCAGAGCAAGCGATGACCTGAAC AGACTCGGTGATTCTCGTCCACTAGAGGCCAAGGCCTGGGAACCAGAGCAAGCGATGACCTGAAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76549342..76549663 26863196 MeRIP-seq:(Medium) rs527401430 Functional Loss SNV dbSNP153 33..33 33 - - - 73802 RMVar_ID_73802 Human_SNP_ID_326775788 m1A Human chr7 + 76549555 76549555 76549555 GCGTGAACCCCGGAGCCGGCGGCGCTGGGGCCAGAGGGGCCGGGCGGGAGGTGATGGCGGAGGCG GCGTGAACCCCGGAGCCGGCGGCGCTGGGGCCGGAGGGGCCGGGCGGGAGGTGATGGCGGAGGCG A G AC004980.1 Ensembl:ENSG00000205485 Pseudogene exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:76549473..76549604 26863196 MeRIP-seq:(Medium) rs1377423638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5328484,Human_RBP_ID_5623711,Human_RBP_ID_9439281,Human_RBP_ID_18426036 73803 RMVar_ID_73803 Human_SNP_ID_326775813 m1A Human chr7 + 76549630 76549630 76549630 GGGACCTGGGCCTGGCCCGTGTGTGTCCTCAGAGGCCTGGCGCCGGCCGTCGCTGTACGGTGAGC GGGACCTGGGCCTGGCCCGTGTGTGTCCTCAGCGGCCTGGCGCCGGCCGTCGCTGTACGGTGAGC A C AC004980.1 Ensembl:ENSG00000205485 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:76549606..76549804 26863196 MeRIP-seq:(Medium) rs904121432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87800,Human_RBP_ID_794650,Human_RBP_ID_3868277,Human_RBP_ID_5220829,Human_RBP_ID_5328484,Human_RBP_ID_9337208,Human_RBP_ID_9404598,Human_RBP_ID_9439281,Human_RBP_ID_18426357,Human_RBP_ID_22112594,Human_RBP_ID_26772065 Human_Splice_Rec_879781 73804 RMVar_ID_73804 Human_SNP_ID_326794959 m1A Human chr7 + 76626790 76626790 76626790 GTAAAAGTGGTGAACGCGATGGGTCGGCGGGGAGGGCGGTGTGGAGCGCGGCGCCGGGCGGGCGG GTAAAAGTGGTGAACGCGATGGGTCGGCGGGGCGGGCGGTGTGGAGCGCGGCGCCGGGCGGGCGG A C AC004980.1 Ensembl:ENSG00000205485 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76626698..76626860;chr7:76626698..76626867 26863196 MeRIP-seq:(Medium) rs1375811632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3862439,Human_RBP_ID_8220667,Human_RBP_ID_22366603,Human_RBP_ID_22528843,Human_RBP_ID_22728859,Human_RBP_ID_24554950,Human_RBP_ID_26794588 73805 RMVar_ID_73805 Human_SNP_ID_326794963 m1A Human chr7 - 76626797 76626796 76626797 CCGCCGCCCGCCCGCCCGGCGCCGCGCTCCACACCGCCCTCCCCGCCGACCCATCGCGTTCACCA CCGCCGCCCGCCCGCCCGGCGCCGCGCTCCAC_CCGCCCTCCCCGCCGACCCATCGCGTTCACCA GT G POMZP3 Ensembl:ENSG00000146707 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:76626649..76626847;chr7:76626718..76626860 26863196 MeRIP-seq:(Medium) rs1183827600 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_879787,Human_Splice_Rec_879795,Human_Splice_Rec_879813 RMVar_hsa_circ_124331,RMVar_hsa_circ_245851 73806 RMVar_ID_73806 Human_SNP_ID_326795001 m1A Human chr7 - 76626837 76626837 76626837 CCCCCGCTCCGGAGGGCCAGGACCTGCGGAATAGGCCTGGCCGCCGCCCGCCCGCCCGGCGCCGC CCCCCGCTCCGGAGGGCCAGGACCTGCGGAATCGGCCTGGCCGCCGCCCGCCCGCCCGGCGCCGC T G POMZP3 Ensembl:ENSG00000146707 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:76626797..76626896 26863410 MeRIP-seq:(Medium) rs1193723729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124331,RMVar_hsa_circ_245851 73807 RMVar_ID_73807 Human_SNP_ID_326873064 m1A Human chr7 + 76992343 76992343 76992343 TGCCACAGAGACCGTGGGCGGGACTGAAGAGAAAATGAAGGAGCGGCCAGAGAGGTGGGGGCAGG TGCCACAGAGACCGTGGGCGGGACTGAAGAGAGAATGAAGGAGCGGCCAGAGAGGTGGGGGCAGG A G DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:76992235..76992364 26863196 MeRIP-seq:(Medium) rs534763605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3866699 RMVar_hsa_circ_93577,RMVar_hsa_circ_245860,RMVar_hsa_circ_19157 73808 RMVar_ID_73808 Human_SNP_ID_326874468 m1A Human chr7 - 76997060 76997060 76997060 CACCCACCTCCATACACCCCACACCTCCACACACCTCCACACACACTCCACACCTCCATACACCC CACCCACCTCCATACACCCCACACCTCCACACCCCTCCACACACACTCCACACCTCCATACACCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76997050..76997190 26863196 MeRIP-seq:(Medium) rs1406311393 Functional Loss SNV dbSNP153 33..33 33 - - - 73809 RMVar_ID_73809 Human_SNP_ID_326874521 m1A Human chr7 - 76997162 76997160 76997162 CCCACCTCCACACACCTCACACCCCACCTCACACCCCACACACTTCTACACACCCTACACACCTC CCCACCTCCACACACCTCACACCCCACCTCAC__CCCACACACTTCTACACACCCTACACACCTC GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997003..76997204 26863196 MeRIP-seq:(Medium) rs60297378 Functional Loss DEL dbSNP153 33..34 33 - - - 73810 RMVar_ID_73810 Human_SNP_ID_326874826 m1A Human chr7 - 76997508 76997501 76997508 CACAGACCCCACACTCCACACCTCCACACACCACACACCTCCACACCTCACACATCTCCACACCC CACAGACCCCACACTCCACACCTCCACACACC_______TCCACACCTCACACATCTCCACACCC AGGTGTGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76997506..76997673 26863196 MeRIP-seq:(Medium) rs199925921 Functional Loss DEL dbSNP153 33..39 33 - - - 73811 RMVar_ID_73811 Human_SNP_ID_326874828 m1A Human chr7 - 76997508 76997508 76997508 CACAGACCCCACACTCCACACCTCCACACACCACACACCTCCACACCTCACACATCTCCACACCC CACAGACCCCACACTCCACACCTCCACACACCTCACACCTCCACACCTCACACATCTCCACACCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76997506..76997673 26863196 MeRIP-seq:(Medium) rs200463551 Functional Loss SNV dbSNP153 33..33 33 - - - 73812 RMVar_ID_73812 Human_SNP_ID_326874829 m1A Human chr7 - 76997508 76997508 76997508 CACAGACCCCACACTCCACACCTCCACACACCACACACCTCCACACCTCACACATCTCCACACCC CACAGACCCCACACTCCACACCTCCACACACCCCACACCTCCACACCTCACACATCTCCACACCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76997506..76997673 26863196 MeRIP-seq:(Medium) rs200463551 Functional Loss SNV dbSNP153 33..33 33 - - - 73813 RMVar_ID_73813 Human_SNP_ID_326875106 m1A Human chr7 - 76997841 76997841 76997841 CCCACACCTGTACACACCCCACACCTCCACACACCACACATCTCCACACACACACCACACGTCCA CCCACACCTGTACACACCCCACACCTCCACACCCCACACATCTCCACACACACACCACACGTCCA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:76997838..76997967 26863196 MeRIP-seq:(Medium) rs1489388953 Functional Loss SNV dbSNP153 33..33 33 - - - 73814 RMVar_ID_73814 Human_SNP_ID_326875141 m1A Human chr7 + 76997921 76997906 76997922 GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGAGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG GTGTGCAGGTGTGTGGAA________________GTGTGCAGGTGTGTGGGTATGTGCAGGTGTG AGTGTGCAGGTGTGGAG A DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997737..76998069;chr7:76997261..76998031 26863196 MeRIP-seq:(Medium) rs1212893486 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_3860588,Human_RBP_ID_5219950,Human_RBP_ID_8150528,Human_RBP_ID_8219691 RMVar_hsa_circ_93577,RMVar_hsa_circ_245860 73815 RMVar_ID_73815 Human_SNP_ID_326875151 m1A Human chr7 + 76997921 76997916 76997922 GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGAGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG GTGTGCAGGTGTGTGGAAGTGTGCAGGT______GTGTGCAGGTGTGTGGGTATGTGCAGGTGTG TGTGGAG T DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997737..76998069;chr7:76997261..76998031 26863196 MeRIP-seq:(Medium) rs779506919 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_3860588,Human_RBP_ID_5219950,Human_RBP_ID_8150528,Human_RBP_ID_8219691 RMVar_hsa_circ_93577,RMVar_hsa_circ_245860 73816 RMVar_ID_73816 Human_SNP_ID_326875157 m1A Human chr7 + 76997921 76997921 76997921 GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGAGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGCGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG A C DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997737..76998069;chr7:76997261..76998031 26863196 MeRIP-seq:(Medium) rs200805215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860588,Human_RBP_ID_5219950,Human_RBP_ID_8150528,Human_RBP_ID_8219691 RMVar_hsa_circ_93577,RMVar_hsa_circ_245860 73817 RMVar_ID_73817 Human_SNP_ID_326875158 m1A Human chr7 + 76997921 76997921 76997921 GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGAGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG GTGTGCAGGTGTGTGGAAGTGTGCAGGTGTGGGGGTGTGCAGGTGTGTGGGTATGTGCAGGTGTG A G DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997737..76998069;chr7:76997261..76998031 26863196 MeRIP-seq:(Medium) rs200805215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860588,Human_RBP_ID_5219950,Human_RBP_ID_8150528,Human_RBP_ID_8219691 RMVar_hsa_circ_93577,RMVar_hsa_circ_245860 73818 RMVar_ID_73818 Human_SNP_ID_327040264 m1A Human chr7 + 77662996 77662980 77662997 GGAAGGAACGAAGGAAGGAGACAGAGAGAGGGAAGAAGGAGAGAGAGGAAGGAAGGAGGGAAGGA GGAAGGAACGAAGGAAG_________________GAAGGAGAGAGAGGAAGGAAGGAGGGAAGGA GGAGACAGAGAGAGGGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:77662956..77663130 26863196 MeRIP-seq:(Medium) rs1407100053 Functional Loss DEL dbSNP153 18..34 33 - - - 73819 RMVar_ID_73819 Human_SNP_ID_327040278 m1A Human chr7 + 77662996 77662994 77662997 GGAAGGAACGAAGGAAGGAGACAGAGAGAGGGAAGAAGGAGAGAGAGGAAGGAAGGAGGGAAGGA GGAAGGAACGAAGGAAGGAGACAGAGAGAGG___GAAGGAGAGAGAGGAAGGAAGGAGGGAAGGA GGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:77662956..77663130 26863196 MeRIP-seq:(Medium) rs1479989828 Functional Loss DEL dbSNP153 32..34 33 - - - 73820 RMVar_ID_73820 Human_SNP_ID_327040302 m1A Human chr7 + 77663034 77663031 77663035 GAGAGAGAGGAAGGAAGGAGGGAAGGAAGGAGACAGAGAGAGGAAAGAAGGAGAGAGAGGAAGGA GAGAGAGAGGAAGGAAGGAGGGAAGGAAGG____AGAGAGAGGAAAGAAGGAGAGAGAGGAAGGA GAGAC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:77662985..77663091 26863196 MeRIP-seq:(Medium) rs1382559966 Functional Loss DEL dbSNP153 31..34 33 - - - 73821 RMVar_ID_73821 Human_SNP_ID_327040304 m1A Human chr7 + 77663034 77663033 77663035 GAGAGAGAGGAAGGAAGGAGGGAAGGAAGGAGACAGAGAGAGGAAAGAAGGAGAGAGAGGAAGGA GAGAGAGAGGAAGGAAGGAGGGAAGGAAGGAG__AGAGAGAGGAAAGAAGGAGAGAGAGGAAGGA GAC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:77662985..77663091 26863196 MeRIP-seq:(Medium) rs1469052610 Functional Loss DEL dbSNP153 33..34 33 - - - 73822 RMVar_ID_73822 Human_SNP_ID_327048722 m1A Human chr7 - 77696555 77696555 77696555 GAGAACCCGGAGGGTCCCGGGAGGAGAGTTGCAGCTTGCCAAACGGTTCTTTCTCCGAGACGGTG GAGAACCCGGAGGGTCCCGGGAGGAGAGTTGCGGCTTGCCAAACGGTTCTTTCTCCGAGACGGTG T C APTR,APTR:2,APTR:3,APTR:4,APTR:5,APTR:6,APTR:7,APTR:8,APTR:9 RNACentral:URS0000EBD0CC,RNACentral:URS000075BCAA,RNACentral:URS0000D58728,RNACentral:URS0000D5A265,RNACentral:URS0000D5D1C5,RNACentral:URS0000D597C1,RNACentral:URS00008C21E3,RNACentral:URS00008C0A82,RNACentral:URS0000D5D074 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,intron,exon,exon,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:77696466..77696642 26863410 MeRIP-seq:(Medium) rs547849948 Functional Loss SNV dbSNP153 33..33 33 - - - 73823 RMVar_ID_73823 Human_SNP_ID_327048815 m1A Human chr7 + 77696708 77696708 77696708 GCAGCCGCCGGCAGCACCTTCGCCTCAGAGCTATGGCAGCCCCGCGTCTTGGAGCTTTGCCCCTC GCAGCCGCCGGCAGCACCTTCGCCTCAGAGCTGTGGCAGCCCCGCGTCTTGGAGCTTTGCCCCTC A G RSBN1L Ensembl:ENSG00000187257 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:77696668..77696800 26863196 MeRIP-seq:(Medium) rs753735851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4949742,Human_RBP_ID_8912651,Human_RBP_ID_18885938 Human_miRNA_ID_3065695 RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 73824 RMVar_ID_73824 Human_SNP_ID_327048989 m1A Human chr7 + 77697040 77697040 77697040 GCGGGGCCTCCCGGGAGGAGAACGGGGAGGTGAAGCCGCTGCCCCGAGGTGGGTGCCGTGCGGGG GCGGGGCCTCCCGGGAGGAGAACGGGGAGGTGCAGCCGCTGCCCCGAGGTGGGTGCCGTGCGGGG A C RSBN1L Ensembl:ENSG00000187257 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:77696939..77697184 26863410 MeRIP-seq:(Medium) rs1334117964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_880585 RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 73825 RMVar_ID_73825 Human_SNP_ID_327076250 m1A Human chr7 + 77798854 77798854 77798854 CGGGAGAGGGGGTGGGGCAACCCTCTGGAGGCAGCGCGCCCGCGGGCAGCCTCGTTGTGGCTCCT CGGGAGAGGGGGTGGGGCAACCCTCTGGAGGCTGCGCGCCCGCGGGCAGCCTCGTTGTGGCTCCT A T PHTF2 Ensembl:ENSG00000006576 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:77798803..77799096 26863196 MeRIP-seq:(Medium) rs895751811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956451 Human_miRNA_ID_2713936,Human_miRNA_ID_3049914 RMVar_hsa_circ_100388,RMVar_hsa_circ_245966,RMVar_hsa_circ_83238,RMVar_hsa_circ_245965 73826 RMVar_ID_73826 Human_SNP_ID_327076264 m1A Human chr7 - 77798886 77798886 77798886 TCCGAAGCTAGCGCCGCCGCCAACAGAGCCCAAGGAGCCACAACGAGGCTGCCCGCGGGCGCGCT TCCGAAGCTAGCGCCGCCGCCAACAGAGCCCAGGGAGCCACAACGAGGCTGCCCGCGGGCGCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:77798798..77798928;chr7:77798817..77798943 26863196 MeRIP-seq:(Medium) rs796834205 Functional Loss SNV dbSNP153 33..33 33 - - - 73827 RMVar_ID_73827 Human_SNP_ID_327076282 m1A Human chr7 + 77798948 77798948 77798948 GGAGTCTCCCGCGCGCACCTCAGCCGCCTCCTAGCGGCGCGGCGCTCGCTCCTACGGTAAGAGCG GGAGTCTCCCGCGCGCACCTCAGCCGCCTCCTGGCGGCGCGGCGCTCGCTCCTACGGTAAGAGCG A G PHTF2 Ensembl:ENSG00000006576 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:77798853..77798985 26863410 MeRIP-seq:(Medium) rs1184385516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956451,Human_RBP_ID_5513691 Human_Splice_Rec_880637,Human_Splice_Rec_880675,Human_Splice_Rec_880711,Human_Splice_Rec_880745,Human_Splice_Rec_880767,Human_Splice_Rec_880783 Human_miRNA_ID_2442898 RMVar_hsa_circ_100388,RMVar_hsa_circ_245966,RMVar_hsa_circ_83238,RMVar_hsa_circ_245965 73828 RMVar_ID_73828 Human_SNP_ID_327076406 m1A Human chr7 - 77799379 77799379 77799379 TAGCTGACATCTCCCCGCCAGCCGGGCTAGCCACCCGAGACCCCTGAACGCCCTTCCAGGACCCG TAGCTGACATCTCCCCGCCAGCCGGGCTAGCCCCCCGAGACCCCTGAACGCCCTTCCAGGACCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr7:77799377..77799504;chr7:77799374..77799442 26863196 MeRIP-seq:(Medium) rs1251554506 Functional Loss SNV dbSNP153 33..33 33 - - - 73829 RMVar_ID_73829 Human_SNP_ID_327076412 m1A Human chr7 + 77799400 77799400 77799400 GGGGTCTCGGGTGGCTAGCCCGGCTGGCGGGGAGATGTCAGCTAGCGGCCGGAGGAGCGGGCTCG GGGGTCTCGGGTGGCTAGCCCGGCTGGCGGGGGGATGTCAGCTAGCGGCCGGAGGAGCGGGCTCG A G PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:77799392..77799496 26863196 MeRIP-seq:(Medium) rs988682254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100388,RMVar_hsa_circ_245966,RMVar_hsa_circ_83238,RMVar_hsa_circ_245965 73830 RMVar_ID_73830 Human_SNP_ID_327081604 m1A Human chr7 + 77822081 77822081 77822081 GGATGTATCAGCTGCTTAGAGACGTGGGGGGCACTCTTCCACTTGGAGGGCATATAGCAGTTTTC GGATGTATCAGCTGCTTAGAGACGTGGGGGGCGCTCTTCCACTTGGAGGGCATATAGCAGTTTTC A G PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:77822077..77822360 26863196 MeRIP-seq:(Medium) rs1367839655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100388,RMVar_hsa_circ_245966,RMVar_hsa_circ_83238,RMVar_hsa_circ_245965 73831 RMVar_ID_73831 Human_SNP_ID_327129432 m1A Human chr7 + 78019261 78019261 78019261 AGTGAAAATAAATTAAAACGCCGTGAGACGGAACCTAAGAAGAACTGCCTGCGCCGGGGCGGGCG AGTGAAAATAAATTAAAACGCCGTGAGACGGACCCTAAGAAGAACTGCCTGCGCCGGGGCGGGCG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:78019210..78019356 32194978 MeRIP-seq:(Medium) rs1429613690 Functional Loss SNV dbSNP153 33..33 33 - - - 73832 RMVar_ID_73832 Human_SNP_ID_327129714 m1A Human chr7 - 78019767 78019767 78019767 GGAAACCAAAGGAGCTTTCAGCCTGCGGCCAGAAGAAGCAGCGCCTCGGGGAGCAGAGGGAGCGC GGAAACCAAAGGAGCTTTCAGCCTGCGGCCAGGAGAAGCAGCGCCTCGGGGAGCAGAGGGAGCGC T C MAGI2 Ensembl:ENSG00000187391 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:78019504..78019805 26863196 MeRIP-seq:(Medium) rs1417765409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245991 73833 RMVar_ID_73833 Human_SNP_ID_327659345 m1A Human chr7 + 80134899 80134899 80134899 ACCGGCGGGAGTGCAGCGGCCACTGTACCCAGAGATTCAAAACCCCAAACCCGGGACTTGGGGGC ACCGGCGGGAGTGCAGCGGCCACTGTACCCAGGGATTCAAAACCCCAAACCCGGGACTTGGGGGC A G GNAI1 Ensembl:ENSG00000127955 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:80134849..80135250 26863196 MeRIP-seq:(Medium) rs1340177947 Functional Loss SNV dbSNP153 33..33 33 - - - 73834 RMVar_ID_73834 Human_SNP_ID_327667136 m1A Human chr7 - 80162769 80162766 80162770 CCCATCCATTGTGCTCAGCCACACCAAATCCCAGTGTGTGGCTGAATAAGGACCATTTTATTACT CCCATCCATTGTGCTCAGCCACACCAAATCC____GTGTGGCTGAATAAGGACCATTTTATTACT CACTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:80162767..80162870 26863196 MeRIP-seq:(Medium) rs1424189076 Functional Loss DEL dbSNP153 32..35 33 - - - 73835 RMVar_ID_73835 Human_SNP_ID_327831172 m1A Human chr7 - 80814836 80814836 80814836 GTACTCAGGTGATAGCAATGGTGACAGAGAGTATAAAATGGTATGAAGTATAAAATAGTATAGAT GTACTCAGGTGATAGCAATGGTGACAGAGAGTGTAAAATGGTATGAAGTATAAAATAGTATAGAT T C SEMA3C Ensembl:ENSG00000075223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:80814793..80814948 26863196 MeRIP-seq:(Medium) rs892137421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6927,RMVar_hsa_circ_89501,RMVar_hsa_circ_246034,RMVar_hsa_circ_246036,RMVar_hsa_circ_358136,RMVar_hsa_circ_246052,RMVar_hsa_circ_93235,RMVar_hsa_circ_246047,RMVar_hsa_circ_295941,RMVar_hsa_circ_295002,RMVar_hsa_circ_127114,RMVar_hsa_circ_25412,RMVar_hsa_circ_91346,RMVar_hsa_circ_246054,RMVar_hsa_circ_246053,RMVar_hsa_circ_246050,RMVar_hsa_circ_246051,RMVar_hsa_circ_289646,RMVar_hsa_circ_246064,RMVar_hsa_circ_246065,RMVar_hsa_circ_46366,RMVar_hsa_circ_78695,RMVar_hsa_circ_246068,RMVar_hsa_circ_246069,RMVar_hsa_circ_275429 73836 RMVar_ID_73836 Human_SNP_ID_327857103 m1A Human chr7 - 80918902 80918902 80918902 CGACGTGCTAGAAAATAAGGTCGTCTGGGAAAAGGACTGGAGACACAAGCGCATCCAACCCCGGT CGACGTGCTAGAAAATAAGGTCGTCTGGGAAAGGGACTGGAGACACAAGCGCATCCAACCCCGGT T C SEMA3C Ensembl:ENSG00000075223 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:80918851..80919058 26863196 MeRIP-seq:(Medium) rs941256457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173884,Human_RBP_ID_4965285,Human_RBP_ID_18104630 Human_Splice_Rec_882677,Human_Splice_Rec_882745,Human_Splice_Rec_882773,Human_Splice_Rec_882781,Human_Splice_Rec_882785 Human_miRNA_ID_2929894 RMVar_hsa_circ_114775,RMVar_hsa_circ_246074 73837 RMVar_ID_73837 Human_SNP_ID_327857185 m1A Human chr7 - 80919127 80919126 80919127 TGATGCGAGCCTGCAGGGCGGCGCGCCGGGGCAGCCGGAGCCGCGCGCCGCGGCGCTGTAATCGG TGATGCGAGCCTGCAGGGCGGCGCGCCGGGGC_GCCGGAGCCGCGCGCCGCGGCGCTGTAATCGG CT C SEMA3C Ensembl:ENSG00000075223 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:80919083..80919171 26863196 MeRIP-seq:(Medium) rs1210734498 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_2151114,Human_miRNA_ID_2419596 RMVar_hsa_circ_114775,RMVar_hsa_circ_246074 73838 RMVar_ID_73838 Human_SNP_ID_329356880 m1A Human chr7 - 86934857 86934857 86934857 GGTGGGTTGGTAGAGGTACTATTTGGTTAGAGAGAAGGTCTGGAGGCGAGGAAGGAAAGACCATG GGTGGGTTGGTAGAGGTACTATTTGGTTAGAGGGAAGGTCTGGAGGCGAGGAAGGAAAGACCATG T C KIAA1324L Ensembl:ENSG00000164659 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:86934807..86934972 26863196 MeRIP-seq:(Medium) rs1393300744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21233,RMVar_hsa_circ_3484,RMVar_hsa_circ_16417,RMVar_hsa_circ_349044,RMVar_hsa_circ_269737,RMVar_hsa_circ_73260,RMVar_hsa_circ_246226,RMVar_hsa_circ_291865,RMVar_hsa_circ_304396,RMVar_hsa_circ_246229,RMVar_hsa_circ_25455,RMVar_hsa_circ_246230 73839 RMVar_ID_73839 Human_SNP_ID_329385984 m1A Human chr7 - 87059555 87059554 87059555 CCGGGAGCCGGAGCTGCCGCCGCACCCCGGGAAGGCTGCCTTGCCGCCGGCCCGCCGACCGCGGC CCGGGAGCCGGAGCTGCCGCCGCACCCCGGGA_GGCTGCCTTGCCGCCGGCCCGCCGACCGCGGC CT C KIAA1324L Ensembl:ENSG00000164659 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87059518..87059669 26863196 MeRIP-seq:(Medium) rs1163079290 Functional Loss DEL dbSNP153 33..33 33 - - - 73840 RMVar_ID_73840 Human_SNP_ID_329407401 m1A Human chr7 - 87152828 87152828 87152828 CCGAAGCCGCCGCCATTTTCCGCCCCCGCCGGATCGCCGCTGTGCCTCGGCAGCCGCTCGCTTCC CCGAAGCCGCCGCCATTTTCCGCCCCCGCCGGCTCGCCGCTGTGCCTCGGCAGCCGCTCGCTTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:87152673..87153022 26863196 MeRIP-seq:(Medium) rs1390009735 Functional Loss SNV dbSNP153 33..33 33 - - - 73841 RMVar_ID_73841 Human_SNP_ID_329422326 m1A Human chr7 - 87209431 87209427 87209431 TCTGTCTGTCTCACTGTCTCAATCTCTGTCTCACTCTCTTTCACTCTCGCTCTCTCATTCACTAT TCTGTCTGTCTCACTGTCTCAATCTCTGTCTC____TCTTTCACTCTCGCTCTCTCATTCACTAT AGAGT A TMEM243 Ensembl:ENSG00000135185 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:87209429..87209666 26863196 MeRIP-seq:(Medium) rs1475395787 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_21555408 RMVar_hsa_circ_2464 73842 RMVar_ID_73842 Human_SNP_ID_329422328 m1A Human chr7 - 87209431 87209429 87209431 TCTGTCTGTCTCACTGTCTCAATCTCTGTCTCACTCTCTTTCACTCTCGCTCTCTCATTCACTAT TCTGTCTGTCTCACTGTCTCAATCTCTGTCTC__TCTCTTTCACTCTCGCTCTCTCATTCACTAT AGT A TMEM243 Ensembl:ENSG00000135185 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:87209429..87209666 26863196 MeRIP-seq:(Medium) rs1180031184 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_21555408 RMVar_hsa_circ_2464 73843 RMVar_ID_73843 Human_SNP_ID_329422330 m1A Human chr7 - 87209431 87209431 87209431 TCTGTCTGTCTCACTGTCTCAATCTCTGTCTCACTCTCTTTCACTCTCGCTCTCTCATTCACTAT TCTGTCTGTCTCACTGTCTCAATCTCTGTCTCTCTCTCTTTCACTCTCGCTCTCTCATTCACTAT T A TMEM243 Ensembl:ENSG00000135185 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:87209429..87209666 26863196 MeRIP-seq:(Medium) rs1242197559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21555408 RMVar_hsa_circ_2464 73844 RMVar_ID_73844 Human_SNP_ID_329425327 m1A Human chr7 - 87219607 87219607 87219607 GCCAGCGCTTCCCCGACCACTCGGGTTCGGCTATGCGGGAGCCGTGAGGAGGAGGCTTGCAGTCG GCCAGCGCTTCCCCGACCACTCGGGTTCGGCTGTGCGGGAGCCGTGAGGAGGAGGCTTGCAGTCG T C TMEM243 Ensembl:ENSG00000135185 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87219557..87220290 26863196 MeRIP-seq:(Medium) rs955579237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689101,Human_RBP_ID_3862464,Human_RBP_ID_4965355 RMVar_hsa_circ_2464 73845 RMVar_ID_73845 Human_SNP_ID_329425328 m1A Human chr7 - 87219607 87219607 87219607 GCCAGCGCTTCCCCGACCACTCGGGTTCGGCTATGCGGGAGCCGTGAGGAGGAGGCTTGCAGTCG GCCAGCGCTTCCCCGACCACTCGGGTTCGGCTCTGCGGGAGCCGTGAGGAGGAGGCTTGCAGTCG T G TMEM243 Ensembl:ENSG00000135185 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87219557..87220290 26863196 MeRIP-seq:(Medium) rs955579237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689101,Human_RBP_ID_3862464,Human_RBP_ID_4965355 RMVar_hsa_circ_2464 73846 RMVar_ID_73846 Human_SNP_ID_329425335 m1A Human chr7 + 87219619 87219619 87219619 TCCTCCTCACGGCTCCCGCATAGCCGAACCCGAGTGGTCGGGGAAGCGCTGGCGCCAGGGATGGG TCCTCCTCACGGCTCCCGCATAGCCGAACCCGCGTGGTCGGGGAAGCGCTGGCGCCAGGGATGGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:87219501..87219725 26863196 MeRIP-seq:(Medium) rs908649305 Functional Loss SNV dbSNP153 33..33 33 - - - 73847 RMVar_ID_73847 Human_SNP_ID_329425336 m1A Human chr7 - 87219621 87219621 87219621 CACCCATCCCTGGCGCCAGCGCTTCCCCGACCACTCGGGTTCGGCTATGCGGGAGCCGTGAGGAG CACCCATCCCTGGCGCCAGCGCTTCCCCGACCGCTCGGGTTCGGCTATGCGGGAGCCGTGAGGAG T C TMEM243 Ensembl:ENSG00000135185 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:87219570..87220537 26863196 MeRIP-seq:(Medium) rs1029911570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689101,Human_RBP_ID_3862464 Human_Splice_Rec_884612,Human_Splice_Rec_884636 RMVar_hsa_circ_2464 73848 RMVar_ID_73848 Human_SNP_ID_329425337 m1A Human chr7 - 87219621 87219621 87219621 CACCCATCCCTGGCGCCAGCGCTTCCCCGACCACTCGGGTTCGGCTATGCGGGAGCCGTGAGGAG CACCCATCCCTGGCGCCAGCGCTTCCCCGACCCCTCGGGTTCGGCTATGCGGGAGCCGTGAGGAG T G TMEM243 Ensembl:ENSG00000135185 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:87219570..87220537 26863196 MeRIP-seq:(Medium) rs1029911570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689101,Human_RBP_ID_3862464 Human_Splice_Rec_884612,Human_Splice_Rec_884636 RMVar_hsa_circ_2464 73849 RMVar_ID_73849 Human_SNP_ID_329457097 m1A Human chr7 + 87345766 87345766 87345766 GAGGCGGCGAGGCGCGGGCGGTGAGGACGGACAGGTCCGTTGAAGCAGCATTCCCTCCCTCCCCT GAGGCGGCGAGGCGCGGGCGGTGAGGACGGACGGGTCCGTTGAAGCAGCATTCCCTCCCTCCCCT A G CROT Ensembl:ENSG00000005469 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87345730..87346397 26863196 MeRIP-seq:(Medium) rs552115114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956453 Human_Splice_Rec_884677,Human_Splice_Rec_884711,Human_Splice_Rec_884747 73850 RMVar_ID_73850 Human_SNP_ID_329595587 m1A Human chr7 + 87934329 87934329 87934329 CAGCACTGAGCCGCGGTGGAGGTTGCAGCGCCACGGCCGCCGCAGCACCGGCCGGGGCTGGGTGG CAGCACTGAGCCGCGGTGGAGGTTGCAGCGCCGCGGCCGCCGCAGCACCGGCCGGGGCTGGGTGG A G ADAM22 Ensembl:ENSG00000008277 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:87934284..87934557 26863196 MeRIP-seq:(Medium) rs1562783567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4957250 RMVar_hsa_circ_97115,RMVar_hsa_circ_246285 73851 RMVar_ID_73851 Human_SNP_ID_329595622 m1A Human chr7 - 87934430 87934430 87934430 GCTGCCGTCAGCCCGCCTCGCCCGAGACGCTCAGCTCCTCATGCCGGCGCCGCCGAGTCCGTTTC GCTGCCGTCAGCCCGCCTCGCCCGAGACGCTCCGCTCCTCATGCCGGCGCCGCCGAGTCCGTTTC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:87934340..87934466 26863196 MeRIP-seq:(Medium) rs776110522 Functional Loss SNV dbSNP153 33..33 33 - - - 73852 RMVar_ID_73852 Human_SNP_ID_329595627 m1A Human chr7 - 87934436 87934436 87934436 CATGGTGCTGCCGTCAGCCCGCCTCGCCCGAGACGCTCAGCTCCTCATGCCGGCGCCGCCGAGTC CATGGTGCTGCCGTCAGCCCGCCTCGCCCGAGTCGCTCAGCTCCTCATGCCGGCGCCGCCGAGTC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:87934339..87934466 26863196 MeRIP-seq:(Medium) rs181862036 Functional Loss SNV dbSNP153 33..33 33 - - - 73853 RMVar_ID_73853 Human_SNP_ID_329595628 m1A Human chr7 - 87934436 87934436 87934436 CATGGTGCTGCCGTCAGCCCGCCTCGCCCGAGACGCTCAGCTCCTCATGCCGGCGCCGCCGAGTC CATGGTGCTGCCGTCAGCCCGCCTCGCCCGAGCCGCTCAGCTCCTCATGCCGGCGCCGCCGAGTC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:87934339..87934466 26863196 MeRIP-seq:(Medium) rs181862036 Functional Loss SNV dbSNP153 33..33 33 - - - 73854 RMVar_ID_73854 Human_SNP_ID_329595907 m1A Human chr7 + 87935077 87935077 87935077 GCTAGAGAAGAGGAAGGAAAACCGCTTCGTGGAGCGCCAGAGCATCGTGCCACTGCGCCTCATCT GCTAGAGAAGAGGAAGGAAAACCGCTTCGTGGGGCGCCAGAGCATCGTGCCACTGCGCCTCATCT A G ADAM22 Ensembl:ENSG00000008277 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87934987..87935118 26863196 MeRIP-seq:(Medium) rs80075458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18886668 Human_Splice_Rec_885674,Human_Splice_Rec_885732,Human_Splice_Rec_885752,Human_Splice_Rec_885764,Human_Splice_Rec_885820,Human_Splice_Rec_885880 RMVar_hsa_circ_97115,RMVar_hsa_circ_246285 73855 RMVar_ID_73855 Human_SNP_ID_329595908 m1A Human chr7 + 87935077 87935077 87935077 GCTAGAGAAGAGGAAGGAAAACCGCTTCGTGGAGCGCCAGAGCATCGTGCCACTGCGCCTCATCT GCTAGAGAAGAGGAAGGAAAACCGCTTCGTGGTGCGCCAGAGCATCGTGCCACTGCGCCTCATCT A T ADAM22 Ensembl:ENSG00000008277 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:87934987..87935118 26863196 MeRIP-seq:(Medium) rs80075458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18886668 Human_Splice_Rec_885674,Human_Splice_Rec_885732,Human_Splice_Rec_885752,Human_Splice_Rec_885764,Human_Splice_Rec_885820,Human_Splice_Rec_885880 RMVar_hsa_circ_97115,RMVar_hsa_circ_246285 73856 RMVar_ID_73856 Human_SNP_ID_329663019 m1A Human chr7 - 88217103 88217103 88217103 TGGAGGATACAAACGTAAGTTGACAGTCCCAAAGTTTGTCTAAATATACTCTTGTGTTTCCTATC TGGAGGATACAAACGTAAGTTGACAGTCCCAACGTTTGTCTAAATATACTCTTGTGTTTCCTATC T G SRI Ensembl:ENSG00000075142 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:88217101..88217150;chr7:88217101..88217200 26863196 MeRIP-seq:(Medium) rs1256184782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_886044,Human_Splice_Rec_886058,Human_Splice_Rec_886084,Human_Splice_Rec_886096,Human_Splice_Rec_886108,Human_Splice_Rec_886122,Human_Splice_Rec_886132,Human_Splice_Rec_886136 RMVar_hsa_circ_246302,RMVar_hsa_circ_107090,RMVar_hsa_circ_21179,RMVar_hsa_circ_334501 73857 RMVar_ID_73857 Human_SNP_ID_329663048 m1A Human chr7 - 88217190 88217190 88217190 TATTATGATTCCTCTAATTTTTTTTCAAAAGGATGGGCAGATAGATGCTGATGAATTGCAGAGAT TATTATGATTCCTCTAATTTTTTTTCAAAAGGGTGGGCAGATAGATGCTGATGAATTGCAGAGAT T C SRI Ensembl:ENSG00000075142 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:88217176..88217254 26863196 MeRIP-seq:(Medium) rs373729773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953713,Human_RBP_ID_4950670,Human_RBP_ID_8944174 Human_Splice_Rec_886044,Human_Splice_Rec_886045,Human_Splice_Rec_886058,Human_Splice_Rec_886059,Human_Splice_Rec_886073,Human_Splice_Rec_886084,Human_Splice_Rec_886085,Human_Splice_Rec_886096,Human_Splice_Rec_886097,Human_Splice_Rec_886108,Human_Splice_Rec_886109,Human_Splice_Rec_886122,Human_Splice_Rec_886123,Human_Splice_Rec_886132,Human_Splice_Rec_886133,Human_Splice_Rec_886136,Human_Splice_Rec_886137 RMVar_hsa_circ_246302,RMVar_hsa_circ_107090,RMVar_hsa_circ_21179,RMVar_hsa_circ_334501 73858 RMVar_ID_73858 Human_SNP_ID_329663423 m1A Human chr7 - 88218937 88218937 88218937 GACGTGTATGTGTTTCCTGTTTCACAGTATGGAGGGGCTCCCGGAGGGCCTGCGTTTCCCGGACA GACGTGTATGTGTTTCCTGTTTCACAGTATGGGGGGGCTCCCGGAGGGCCTGCGTTTCCCGGACA T C SRI Ensembl:ENSG00000075142 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr7:88218842..88218986;chr7:88218806..88219130;chr7:88218851..88218950 26863196,32194978 MeRIP-seq:(Medium) rs1313536906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794813,Human_RBP_ID_1689286,Human_RBP_ID_4956461,Human_RBP_ID_8944175,Human_RBP_ID_9337217,Human_RBP_ID_22464555 Human_Splice_Rec_886042,Human_Splice_Rec_886043,Human_Splice_Rec_886056,Human_Splice_Rec_886057,Human_Splice_Rec_886083,Human_Splice_Rec_886095,Human_Splice_Rec_886106,Human_Splice_Rec_886107,Human_Splice_Rec_886120,Human_Splice_Rec_886121,Human_Splice_Rec_886130,Human_Splice_Rec_886131,Human_Splice_Rec_886135 RMVar_hsa_circ_21179,RMVar_hsa_circ_334501 73859 RMVar_ID_73859 Human_SNP_ID_329663425 m1A Human chr7 - 88218941 88218941 88218941 GAATGACGTGTATGTGTTTCCTGTTTCACAGTATGGAGGGGCTCCCGGAGGGCCTGCGTTTCCCG GAATGACGTGTATGTGTTTCCTGTTTCACAGTCTGGAGGGGCTCCCGGAGGGCCTGCGTTTCCCG T G SRI Ensembl:ENSG00000075142 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:88218851..88220050 26863410 MeRIP-seq:(Medium) rs749408370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956461,Human_RBP_ID_8944175,Human_RBP_ID_9337217,Human_RBP_ID_22464555 Human_Splice_Rec_886042,Human_Splice_Rec_886043,Human_Splice_Rec_886056,Human_Splice_Rec_886057,Human_Splice_Rec_886083,Human_Splice_Rec_886095,Human_Splice_Rec_886106,Human_Splice_Rec_886107,Human_Splice_Rec_886120,Human_Splice_Rec_886121,Human_Splice_Rec_886130,Human_Splice_Rec_886131,Human_Splice_Rec_886135 RMVar_hsa_circ_21179,RMVar_hsa_circ_334501 73860 RMVar_ID_73860 Human_SNP_ID_329663717 m1A Human chr7 - 88219899 88219899 88219899 CGCTAAGAGGCCACCTTGGAGATGCTGCGGCCAGCGGGGTGAGGCGCTGCTGGGCGGCTACCCGG CGCTAAGAGGCCACCTTGGAGATGCTGCGGCCTGCGGGGTGAGGCGCTGCTGGGCGGCTACCCGG T A SRI Ensembl:ENSG00000075142 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:88219893..88220075 26863196 MeRIP-seq:(Medium) rs1255001941 Functional Loss SNV dbSNP153 33..33 33 - - - 73861 RMVar_ID_73861 Human_SNP_ID_329663792 m1A Human chr7 - 88220026 88220026 88220026 AGGGCGAGGGCGGCTGCGGCGCAGTCTGCAGCATGGCGTACCCGGGGCATCCTGGCGCCGGCGGC AGGGCGAGGGCGGCTGCGGCGCAGTCTGCAGCGTGGCGTACCCGGGGCATCCTGGCGCCGGCGGC T C SRI Ensembl:ENSG00000075142 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:88219914..88220075 26863196 MeRIP-seq:(Medium) rs1487900320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689369,Human_RBP_ID_4950672,Human_RBP_ID_5327896,Human_RBP_ID_9337218,Human_RBP_ID_22464556 Human_Splice_Rec_886041,Human_Splice_Rec_886055,Human_Splice_Rec_886105,Human_Splice_Rec_886119,Human_Splice_Rec_886129 73862 RMVar_ID_73862 Human_SNP_ID_329663793 m1A Human chr7 - 88220026 88220026 88220026 AGGGCGAGGGCGGCTGCGGCGCAGTCTGCAGCATGGCGTACCCGGGGCATCCTGGCGCCGGCGGC AGGGCGAGGGCGGCTGCGGCGCAGTCTGCAGCCTGGCGTACCCGGGGCATCCTGGCGCCGGCGGC T G SRI Ensembl:ENSG00000075142 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:88219914..88220075 26863196 MeRIP-seq:(Medium) rs1487900320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689369,Human_RBP_ID_4950672,Human_RBP_ID_5327896,Human_RBP_ID_9337218,Human_RBP_ID_22464556 Human_Splice_Rec_886041,Human_Splice_Rec_886055,Human_Splice_Rec_886105,Human_Splice_Rec_886119,Human_Splice_Rec_886129 73863 RMVar_ID_73863 Human_SNP_ID_190156438 m1A Human chr4 - 75645501 75645501 75645501 GTGATGGAAGAGGACCTCCTCCAAGGGGTGGCATGGCACAGAAACTTGGCTCTGGAAGAGGAACC GTGATGGAAGAGGACCTCCTCCAAGGGGTGGCGTGGCACAGAAACTTGGCTCTGGAAGAGGAACC T C G3BP2 Ensembl:ENSG00000138757 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:75645451..75645675 26863196 MeRIP-seq:(Medium) rs368804327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72645,Human_RBP_ID_786481,Human_RBP_ID_5150639,Human_RBP_ID_7327476,Human_RBP_ID_9162828,Human_RBP_ID_9304178,Human_RBP_ID_9396401,Human_RBP_ID_15199632,Human_RBP_ID_22457696,Human_RBP_ID_24064268,Human_RBP_ID_26349367 73864 RMVar_ID_73864 Human_SNP_ID_190156446 m1A Human chr4 - 75645520 75645520 75645520 GGTGGAATGATGCGTGATCGTGATGGAAGAGGACCTCCTCCAAGGGGTGGCATGGCACAGAAACT GGTGGAATGATGCGTGATCGTGATGGAAGAGGGCCTCCTCCAAGGGGTGGCATGGCACAGAAACT T C G3BP2 Ensembl:ENSG00000138757 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:75645469..75645675 26863196 MeRIP-seq:(Medium) rs1025359506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786481,Human_RBP_ID_1980927,Human_RBP_ID_5150639,Human_RBP_ID_7327476,Human_RBP_ID_8881041,Human_RBP_ID_9304178,Human_RBP_ID_9396401,Human_RBP_ID_15199635,Human_RBP_ID_22457696,Human_RBP_ID_24064268,Human_RBP_ID_26349367 73865 RMVar_ID_73865 Human_SNP_ID_190163679 m1A Human chr4 - 75673348 75673348 75673348 CTGGCGCCCGGGAAGAGGTGGTTGTGAGGCAGACGAACTCGCGGCTCTCCGGCTTCCGAGGCTTC CTGGCGCCCGGGAAGAGGTGGTTGTGAGGCAGGCGAACTCGCGGCTCTCCGGCTTCCGAGGCTTC T C G3BP2 Ensembl:ENSG00000138757 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:75673201..75673427;chr4:75673201..75673425 26863196 MeRIP-seq:(Medium) rs754221810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249424,Human_RBP_ID_4790269,Human_RBP_ID_8882159,Human_RBP_ID_9304184,Human_RBP_ID_17155651,Human_RBP_ID_22458321,Human_RBP_ID_27070133,Human_RBP_ID_27841841 73866 RMVar_ID_73866 Human_SNP_ID_190176218 m1A Human chr4 - 75724722 75724722 75724722 TCCGCAGGGCCTGGGCCCCAATCCCGCACTCTACACACTCCTACTGCTGCCACCACCGCCTCCAA TCCGCAGGGCCTGGGCCCCAATCCCGCACTCTCCACACTCCTACTGCTGCCACCACCGCCTCCAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:75724576..75724850 26863196 MeRIP-seq:(Medium) rs1272327532 Functional Loss SNV dbSNP153 33..33 33 - - - 73867 RMVar_ID_73867 Human_SNP_ID_190176219 m1A Human chr4 + 75724723 75724723 75724723 TGGAGGCGGTGGTGGCAGCAGTAGGAGTGTGTAGAGTGCGGGATTGGGGCCCAGGCCCTGCGGAG TGGAGGCGGTGGTGGCAGCAGTAGGAGTGTGTGGAGTGCGGGATTGGGGCCCAGGCCCTGCGGAG A G USO1 Ensembl:ENSG00000138768 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:75724634..75724916 26863196 MeRIP-seq:(Medium) rs572975169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72653,Human_RBP_ID_5326020,Human_RBP_ID_8212393,Human_RBP_ID_18424599,Human_RBP_ID_26349376 73868 RMVar_ID_73868 Human_SNP_ID_190176276 m1A Human chr4 + 75724841 75724841 75724841 TGAACGGCAAGATGAATTTCCTCCGCGGGGTAATGGGGGGTCAGAGTGCCGGACCCCAGCACACA TGAACGGCAAGATGAATTTCCTCCGCGGGGTAGTGGGGGGTCAGAGTGCCGGACCCCAGCACACA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs752718287 Functional Loss SNV dbSNP153 33..33 33 - - - 73869 RMVar_ID_73869 Human_SNP_ID_190242698 m1A Human chr4 + 75985383 75985383 75985383 CACTGCTACGTCGTTTCTTTCTCCCAGCATGGATGAGTCAGTAGGCATCCTCCTTTTTCATCAAT CACTGCTACGTCGTTTCTTTCTCCCAGCATGGGTGAGTCAGTAGGCATCCTCCTTTTTCATCAAT A G AC112719.2 Ensembl:ENSG00000245928 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:75985381..75985738 26863196 MeRIP-seq:(Medium) rs916537267 Functional Loss SNV dbSNP153 33..33 33 - - - 73870 RMVar_ID_73870 Human_SNP_ID_190242746 m1A Human chr4 - 75985595 75985595 75985595 ATCACCAAGTATTATAACAGGAATTGAGATAGAGGGTGAGAAGACAGTGAGCAAAGAGCTGAAAT ATCACCAAGTATTATAACAGGAATTGAGATAGTGGGTGAGAAGACAGTGAGCAAAGAGCTGAAAT T A SDAD1 Ensembl:ENSG00000198301 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:75985591..75985728 26863196 MeRIP-seq:(Medium) rs958781103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7327965,Human_RBP_ID_15201417 RMVar_hsa_circ_226654,RMVar_hsa_circ_118048,RMVar_hsa_circ_85567,RMVar_hsa_circ_226667 73871 RMVar_ID_73871 Human_SNP_ID_190242794 m1A Human chr4 + 75985831 75985831 75985831 TATTCCTCTCCAACCACATCTCTTATTTTCCAAACTCCAACGATCCTTCAATCTCATCAGAATCC TATTCCTCTCCAACCACATCTCTTATTTTCCACACTCCAACGATCCTTCAATCTCATCAGAATCC A C AC112719.2 Ensembl:ENSG00000245928 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:75985826..75986005 26863196 MeRIP-seq:(Medium) rs1010128294 Functional Loss SNV dbSNP153 33..33 33 - - - 73872 RMVar_ID_73872 Human_SNP_ID_190242918 m1A Human chr4 - 75986344 75986344 75986344 CAAAGTATGAAATGGTTGTCCAGAAAAGTGGGAAAGTGAAGGGACTAGAGAAATGTAATGAGATT CAAAGTATGAAATGGTTGTCCAGAAAAGTGGGCAAGTGAAGGGACTAGAGAAATGTAATGAGATT T G SDAD1 Ensembl:ENSG00000198301 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:75986339..75986587 26863196 MeRIP-seq:(Medium) rs1192137475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226654,RMVar_hsa_circ_118048,RMVar_hsa_circ_85567,RMVar_hsa_circ_226667 73873 RMVar_ID_73873 Human_SNP_ID_190242921 m1A Human chr4 - 75986352 75986352 75986352 ACAGATTGCAAAGTATGAAATGGTTGTCCAGAAAAGTGGGAAAGTGAAGGGACTAGAGAAATGTA ACAGATTGCAAAGTATGAAATGGTTGTCCAGAGAAGTGGGAAAGTGAAGGGACTAGAGAAATGTA T C SDAD1 Ensembl:ENSG00000198301 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:75986349..75986478 26863196 MeRIP-seq:(Medium) rs1210729759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226654,RMVar_hsa_circ_118048,RMVar_hsa_circ_85567,RMVar_hsa_circ_226667 73874 RMVar_ID_73874 Human_SNP_ID_190244115 m1A Human chr4 + 75990887 75990887 75990887 AGACTTCGCGGCGAGCAGTTTTAAAAAAACTCAGACGGCCGGCACCCCGCAATCCCTGCCAGCTG AGACTTCGCGGCGAGCAGTTTTAAAAAAACTCCGACGGCCGGCACCCCGCAATCCCTGCCAGCTG A C AC112719.2 Ensembl:ENSG00000245928 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:75990813..75990907 26863196 MeRIP-seq:(Medium) rs1202225730 Functional Loss SNV dbSNP153 33..33 33 - - - 73875 RMVar_ID_73875 Human_SNP_ID_190244116 m1A Human chr4 + 75990887 75990887 75990887 AGACTTCGCGGCGAGCAGTTTTAAAAAAACTCAGACGGCCGGCACCCCGCAATCCCTGCCAGCTG AGACTTCGCGGCGAGCAGTTTTAAAAAAACTCTGACGGCCGGCACCCCGCAATCCCTGCCAGCTG A T AC112719.2 Ensembl:ENSG00000245928 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:75990813..75990907 26863196 MeRIP-seq:(Medium) rs1202225730 Functional Loss SNV dbSNP153 33..33 33 - - - 73876 RMVar_ID_73876 Human_SNP_ID_190282612 m1A Human chr4 - 76144475 76144475 76144475 TTCTTCCTTTCTATTTTTGTTCTTTTTTAATTAGGTGGGTTTGGAGGATTTGGGACAACATCTAC TTCTTCCTTTCTATTTTTGTTCTTTTTTAATTGGGTGGGTTTGGAGGATTTGGGACAACATCTAC T C NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:76144442..76144515 26863196 MeRIP-seq:(Medium) rs1560693477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795003,Human_RBP_ID_7328202,Human_RBP_ID_15202084 Human_Splice_Rec_570769,Human_Splice_Rec_570787,Human_Splice_Rec_570813,Human_Splice_Rec_570839,Human_Splice_Rec_570859,Human_Splice_Rec_570889,Human_Splice_Rec_570897,Human_Splice_Rec_570905,Human_Splice_Rec_570913,Human_Splice_Rec_570919,Human_Splice_Rec_570923,Human_Splice_Rec_570929,Human_Splice_Rec_570937 RMVar_hsa_circ_110611,RMVar_hsa_circ_226686 73877 RMVar_ID_73877 Human_SNP_ID_190299060 m1A Human chr4 + 76213790 76213789 76213790 CCCGGACTCGGTTTCGGTTTCCTTCGCCGGGCAGCCGTGGCGCCCGCCTAGCGCAGCTCGGGAGA CCCGGACTCGGTTTCGGTTTCCTTCGCCGGGC_GCCGTGGCGCCCGCCTAGCGCAGCTCGGGAGA CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:76213739..76213854 26863196 MeRIP-seq:(Medium) rs554503994 Functional Loss DEL dbSNP153 33..33 33 - - - 73878 RMVar_ID_73878 Human_SNP_ID_190299062 m1A Human chr4 + 76213790 76213790 76213790 CCCGGACTCGGTTTCGGTTTCCTTCGCCGGGCAGCCGTGGCGCCCGCCTAGCGCAGCTCGGGAGA CCCGGACTCGGTTTCGGTTTCCTTCGCCGGGCGGCCGTGGCGCCCGCCTAGCGCAGCTCGGGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:76213739..76213854 26863196 MeRIP-seq:(Medium) rs925868996 Functional Loss SNV dbSNP153 33..33 33 - - - 73879 RMVar_ID_73879 Human_SNP_ID_190319360 m1A Human chr4 + 76306166 76306166 76306166 GGAGCTTCCACTAGGGCTCCCAGTTTCCCCGCACCGCGCCCGCCGTCCTCCGGGCCACCCATCCC GGAGCTTCCACTAGGGCTCCCAGTTTCCCCGCCCCGCGCCCGCCGTCCTCCGGGCCACCCATCCC A C STBD1,FAM47E-STBD1 Ensembl:ENSG00000118804,Ensembl:ENSG00000272414 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:76306126..76306282 26863196 MeRIP-seq:(Medium) rs112251880 Functional Loss SNV dbSNP153 33..33 33 - - - 73880 RMVar_ID_73880 Human_SNP_ID_190319610 m1A Human chr4 - 76306900 76306900 76306900 TCTGATGGCCTCCCGGAATCGCAGCTCCCCCAAGAGGGGCGTCTTTCTCCTGCTCCGCATCCCCG TCTGATGGCCTCCCGGAATCGCAGCTCCCCCAGGAGGGGCGTCTTTCTCCTGCTCCGCATCCCCG T C AC034139.1 Ensembl:ENSG00000287401 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:76306688..76306956 26863196 MeRIP-seq:(Medium) rs1315548646 Functional Loss SNV dbSNP153 33..33 33 - - - 73881 RMVar_ID_73881 Human_SNP_ID_190320470 m1A Human chr4 - 76309896 76309896 76309896 TTCCCAGCGGGTAACTCCCCCATTCTCTACCAACACAAACTTCCACTCCACCACTGTATCTGCAG TTCCCAGCGGGTAACTCCCCCATTCTCTACCAGCACAAACTTCCACTCCACCACTGTATCTGCAG T C AC034139.1 Ensembl:ENSG00000287401 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:76309846..76309972 26863196 MeRIP-seq:(Medium) rs1373162979 Functional Loss SNV dbSNP153 33..33 33 - - - 73882 RMVar_ID_73882 Human_SNP_ID_190469118 m1A Human chr4 - 76948543 76948541 76948543 GGGCGGGGAACCAGCTGGGTGGAAGCACAGGGAGTGTGGTGAGGAGGGAAGGGCTGTGATCTGCC GGGCGGGGAACCAGCTGGGTGGAAGCACAGGG__TGTGGTGAGGAGGGAAGGGCTGTGATCTGCC ACT A lnc-SOWAHB-5,lnc-SOWAHB-5:2,lnc-SOWAHB-5:3,lnc-SOWAHB-5:4,lnc-SOWAHB-5:5,lnc-SOWAHB-5:6,lnc-SOWAHB-5:7,lnc-SOWAHB-5:8,lnc-SOWAHB-5:9 RNACentral:URS0000D5D8AE,RNACentral:URS00009BE28C,RNACentral:URS0000D5BF93,RNACentral:URS0000D594A0,RNACentral:URS0000D5C032,RNACentral:URS0000D5A9B5,RNACentral:URS0000D58B58,RNACentral:URS0000D5977F,RNACentral:URS00008B52CA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,exon,exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:76948495..76948624 26863196 MeRIP-seq:(Medium) rs1297091364 Functional Loss DEL dbSNP153 33..34 33 - - - 73883 RMVar_ID_73883 Human_SNP_ID_190469119 m1A Human chr4 - 76948543 76948543 76948543 GGGCGGGGAACCAGCTGGGTGGAAGCACAGGGAGTGTGGTGAGGAGGGAAGGGCTGTGATCTGCC GGGCGGGGAACCAGCTGGGTGGAAGCACAGGGTGTGTGGTGAGGAGGGAAGGGCTGTGATCTGCC T A lnc-SOWAHB-5,lnc-SOWAHB-5:2,lnc-SOWAHB-5:3,lnc-SOWAHB-5:4,lnc-SOWAHB-5:5,lnc-SOWAHB-5:6,lnc-SOWAHB-5:7,lnc-SOWAHB-5:8,lnc-SOWAHB-5:9 RNACentral:URS0000D5D8AE,RNACentral:URS00009BE28C,RNACentral:URS0000D5BF93,RNACentral:URS0000D594A0,RNACentral:URS0000D5C032,RNACentral:URS0000D5A9B5,RNACentral:URS0000D58B58,RNACentral:URS0000D5977F,RNACentral:URS00008B52CA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,exon,exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:76948495..76948624 26863196 MeRIP-seq:(Medium) rs900649165 Functional Loss SNV dbSNP153 33..33 33 - - - 73884 RMVar_ID_73884 Human_SNP_ID_190469152 m1A Human chr4 + 76948648 76948648 76948648 CCTCTCCGGCCCACGTGGGGCCGCAGGGATCCACAGCTCATCTGACACACCTCGCTGCCCTGCAC CCTCTCCGGCCCACGTGGGGCCGCAGGGATCCCCAGCTCATCTGACACACCTCGCTGCCCTGCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:76948601..76948735 26863196 MeRIP-seq:(Medium) rs909944016 Functional Loss SNV dbSNP153 33..33 33 - - - 73885 RMVar_ID_73885 Human_SNP_ID_190482753 m1A Human chr4 - 77011512 77011512 77011512 CATTTGTAGCAGCCCGCCCCCCACCCATGTCAAGCCCTTATTTCCTCTGTGTCTTTGCTCACGCT CATTTGTAGCAGCCCGCCCCCCACCCATGTCATGCCCTTATTTCCTCTGTGTCTTTGCTCACGCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77011509..77011634 26863196 MeRIP-seq:(Medium) rs1351956699 Functional Loss SNV dbSNP153 33..33 33 - - - 73886 RMVar_ID_73886 Human_SNP_ID_190496569 m1A Human chr4 - 77066376 77066376 77066376 TAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGATCCAAAGGATATCATGAAGTTTCCAGGGCCTT TAGGTAGCTACAGCAAGCTGGGTAGCAGGCAGCTCCAAAGGATATCATGAAGTTTCCAGGGCCTT T G CCNI Ensembl:ENSG00000118816 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77066326..77074830 26863196 MeRIP-seq:(Medium) rs1305512297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_624771,Human_RBP_ID_785865,Human_RBP_ID_939999,Human_RBP_ID_1981192,Human_RBP_ID_7329163,Human_RBP_ID_9163093,Human_RBP_ID_15204310,Human_RBP_ID_17295417,Human_RBP_ID_18029752,Human_RBP_ID_22826501,Human_RBP_ID_24065279,Human_RBP_ID_25829260,Human_RBP_ID_26518129 Human_Splice_Rec_571758,Human_Splice_Rec_571776,Human_Splice_Rec_571782,Human_Splice_Rec_571796,Human_Splice_Rec_571802 Human_miRNA_ID_2617097 RMVar_hsa_circ_101854,RMVar_hsa_circ_377992,RMVar_hsa_circ_226747,RMVar_hsa_circ_226748,RMVar_hsa_circ_226751,RMVar_hsa_circ_272672,RMVar_hsa_circ_226754,RMVar_hsa_circ_295656,RMVar_hsa_circ_226753,RMVar_hsa_circ_109366,RMVar_hsa_circ_308793,RMVar_hsa_circ_226755,RMVar_hsa_circ_270560,RMVar_hsa_circ_226756,RMVar_hsa_circ_277672 73887 RMVar_ID_73887 Human_SNP_ID_190496580 m1A Human chr4 + 77066400 77066400 77066400 CCTTTGGATCTGCCTGCTACCCAGCTTGCTGTAGCTACCTACAGAATCAAGTAAGTTTTAAAATT CCTTTGGATCTGCCTGCTACCCAGCTTGCTGTGGCTACCTACAGAATCAAGTAAGTTTTAAAATT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:77066326..77074830;chr4:77066351..77066425 26863196 MeRIP-seq:(Medium) rs778178511 Functional Loss SNV dbSNP153 33..33 33 - - - 73888 RMVar_ID_73888 Human_SNP_ID_190499496 m1A Human chr4 + 77075557 77075557 77075557 AGTGGTGACGCGGGGTCATCCGGGGGCCCGTTACCACCTCATTCTCATAGGCGCGCGGAGGCGGT AGTGGTGACGCGGGGTCATCCGGGGGCCCGTTGCCACCTCATTCTCATAGGCGCGCGGAGGCGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77075446..77075975 26863196 MeRIP-seq:(Medium) rs1325283137 Functional Loss SNV dbSNP153 33..33 33 - - - 73889 RMVar_ID_73889 Human_SNP_ID_190499510 m1A Human chr4 + 77075583 77075583 77075583 CCCGTTACCACCTCATTCTCATAGGCGCGCGGAGGCGGTGCGCGCGGGACGACTCGGCCAACTGA CCCGTTACCACCTCATTCTCATAGGCGCGCGGCGGCGGTGCGCGCGGGACGACTCGGCCAACTGA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:77075451..77075756 26863196 MeRIP-seq:(Medium) rs1326060682 Functional Loss SNV dbSNP153 33..33 33 - - - 73890 RMVar_ID_73890 Human_SNP_ID_190499518 m1A Human chr4 + 77075599 77075599 77075599 TCTCATAGGCGCGCGGAGGCGGTGCGCGCGGGACGACTCGGCCAACTGAGGAGGGAGAAAGGGGA TCTCATAGGCGCGCGGAGGCGGTGCGCGCGGGGCGACTCGGCCAACTGAGGAGGGAGAAAGGGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77075431..77075800 26863196 MeRIP-seq:(Medium) rs1391834554 Functional Loss SNV dbSNP153 33..33 33 - - - 73891 RMVar_ID_73891 Human_SNP_ID_190499695 m1A Human chr4 + 77075903 77075903 77075903 GGGGGGGAGGGGAGAAAAGAAAAGAAAAAAAAAAAAAGAAAGGGGAAAGGGGGGAAAAATAAGAA GGGGGGGAGGGGAGAAAAGAAAAGAAAAAAAAGAAAAGAAAGGGGAAAGGGGGGAAAAATAAGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77075854..77075958 26863196 MeRIP-seq:(Medium) rs1405551649 Functional Loss SNV dbSNP153 33..33 33 - - - 73892 RMVar_ID_73892 Human_SNP_ID_190519111 m1A Human chr4 + 77157351 77157351 77157351 GGGAGCGGGATGGAGCCGGGGCTGTGAGGCCGAGGCGGCGGTGCCTGGGAGGAAGGGTCGGATGC GGGAGCGGGATGGAGCCGGGGCTGTGAGGCCGGGGCGGCGGTGCCTGGGAGGAAGGGTCGGATGC A G CCNG2 Ensembl:ENSG00000138764 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77157204..77158339 26863196 MeRIP-seq:(Medium) rs1464624498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12129,Human_RBP_ID_249425,Human_RBP_ID_266773,Human_RBP_ID_939692,Human_RBP_ID_3747442,Human_RBP_ID_3966289,Human_RBP_ID_4794634,Human_RBP_ID_5089911,Human_RBP_ID_5150747,Human_RBP_ID_5326023,Human_RBP_ID_8130516,Human_RBP_ID_8212020,Human_RBP_ID_8236315,Human_RBP_ID_8943690,Human_RBP_ID_9334724,Human_RBP_ID_9435812,Human_RBP_ID_17409263,Human_RBP_ID_18170323,Human_RBP_ID_18424600,Human_RBP_ID_18500993,Human_RBP_ID_22364231,Human_RBP_ID_26771346,Human_RBP_ID_26791153 73893 RMVar_ID_73893 Human_SNP_ID_190519172 m1A Human chr4 + 77157472 77157472 77157472 GCCCCCGCTGCGCCCAGTCCGTGCGGACCGCGAGGCCGCGGGCGGGTGGAGGCGCGTCTCCGGCA GCCCCCGCTGCGCCCAGTCCGTGCGGACCGCGCGGCCGCGGGCGGGTGGAGGCGCGTCTCCGGCA A C CCNG2 Ensembl:ENSG00000138764 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:77157251..77157525 26863196 MeRIP-seq:(Medium) rs4150048 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_4791120,Human_RBP_ID_22610127 Human_Splice_Rec_571803,Human_Splice_Rec_571819,Human_Splice_Rec_571833 73894 RMVar_ID_73894 Human_SNP_ID_190519575 m1A Human chr4 - 77158478 77158478 77158478 AGAATGTAATCTGGGGGTAAGAGGGGTGGGGAAGCGGGAGAAAGGGCTGAGGCCAGTACCTCCAG AGAATGTAATCTGGGGGTAAGAGGGGTGGGGAGGCGGGAGAAAGGGCTGAGGCCAGTACCTCCAG T C lnc-CCNI-3 RNACentral:URS00008BF57F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:77158477..77158625 26863196 MeRIP-seq:(Medium) rs1248640593 Functional Loss SNV dbSNP153 33..33 33 - - - 73895 RMVar_ID_73895 Human_SNP_ID_190519583 m1A Human chr4 - 77158489 77158488 77158489 ACACCACACAGAGAATGTAATCTGGGGGTAAGAGGGGTGGGGAAGCGGGAGAAAGGGCTGAGGCC ACACCACACAGAGAATGTAATCTGGGGGTAAG_GGGGTGGGGAAGCGGGAGAAAGGGCTGAGGCC CT C lnc-CCNI-3 RNACentral:URS00008BF57F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77158487..77158638 26863196 MeRIP-seq:(Medium) rs756729821 Functional Loss DEL dbSNP153 33..33 33 - - - 73896 RMVar_ID_73896 Human_SNP_ID_190695616 m1A Human chr4 + 77819196 77819196 77819196 CTCGGGCCGCCTCCCCGCCCGCCAAAGTCCCAACTCGCACACCCACACGCACATTTGTCCCTCTC CTCGGGCCGCCTCCCCGCCCGCCAAAGTCCCACCTCGCACACCCACACGCACATTTGTCCCTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77819177..77819318 26863196 MeRIP-seq:(Medium) rs536752989 Functional Loss SNV dbSNP153 33..33 33 - - - 73897 RMVar_ID_73897 Human_SNP_ID_190695617 m1A Human chr4 + 77819196 77819196 77819196 CTCGGGCCGCCTCCCCGCCCGCCAAAGTCCCAACTCGCACACCCACACGCACATTTGTCCCTCTC CTCGGGCCGCCTCCCCGCCCGCCAAAGTCCCAGCTCGCACACCCACACGCACATTTGTCCCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77819177..77819318 26863196 MeRIP-seq:(Medium) rs536752989 Functional Loss SNV dbSNP153 33..33 33 - - - 73898 RMVar_ID_73898 Human_SNP_ID_190695804 m1A Human chr4 - 77819610 77819610 77819610 GCCCCGTCGCCGCCGCCGCCGCCGCCGCCCGGACCCCGGCGCGCTGAATGCAGGTGAGGAGGGGG GCCCCGTCGCCGCCGCCGCCGCCGCCGCCCGGCCCCCGGCGCGCTGAATGCAGGTGAGGAGGGGG T G CNOT6L Ensembl:ENSG00000138767 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77776366..77819712 26863196 MeRIP-seq:(Medium) rs1007327335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9335034 Human_Splice_Rec_571973 73899 RMVar_ID_73899 Human_SNP_ID_190695896 m1A Human chr4 + 77819816 77819816 77819816 CCGCCTGACGAACGGCAGAGGCGGCGGCGCGGAAGGCGGCTGAAGGGAGCGAGGAGACAGACCGG CCGCCTGACGAACGGCAGAGGCGGCGGCGCGGCAGGCGGCTGAAGGGAGCGAGGAGACAGACCGG A C HSALNG0035377 RNACentral:URS0000E964B0 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:77819718..77819922 26863196 MeRIP-seq:(Medium) rs909419254 Functional Loss SNV dbSNP153 33..33 33 - - - 73900 RMVar_ID_73900 Human_SNP_ID_190695931 m1A Human chr4 + 77819916 77819916 77819916 CTTCGAGGACAGTGACCCCAGGCGCGCAAGAGAGGCCCCGCGGCCGCGGCCGCCGGCGCGAAGGC CTTCGAGGACAGTGACCCCAGGCGCGCAAGAGGGGCCCCGCGGCCGCGGCCGCCGGCGCGAAGGC A G HSALNG0035377 RNACentral:URS0000E964B0 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:77819871..77819959 26863196 MeRIP-seq:(Medium) rs1198327116 Functional Loss SNV dbSNP153 33..33 33 - - - 73901 RMVar_ID_73901 Human_SNP_ID_190714749 m1A Human chr4 + 77900845 77900842 77900846 TAGGGTAGCCATATGAGGATGGTGAAACTTTAAGAACAGAGACCAGCGAGGAGGCGATTACAGTA TAGGGTAGCCATATGAGGATGGTGAAACTT____AACAGAGACCAGCGAGGAGGCGATTACAGTA TTAAG T MRPL1 Ensembl:ENSG00000169288 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:77900773..77900939 26863196 MeRIP-seq:(Medium) rs1043791308 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_15205570 RMVar_hsa_circ_21568,RMVar_hsa_circ_292404,RMVar_hsa_circ_48329,RMVar_hsa_circ_306363,RMVar_hsa_circ_82893,RMVar_hsa_circ_226776 73902 RMVar_ID_73902 Human_SNP_ID_190873175 m1A Human chr4 + 78551799 78551799 78551799 GCCAGCGCGGAGCACCTGCGCCCGCGGCTGACACCTTCGCTCGCAGTTTGTTCGCAGTTTACTCG GCCAGCGCGGAGCACCTGCGCCCGCGGCTGACTCCTTCGCTCGCAGTTTGTTCGCAGTTTACTCG A T ANXA3 Ensembl:ENSG00000138772 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:78551598..78551823 26863196 MeRIP-seq:(Medium) rs1040312307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795011 Human_Splice_Rec_572407,Human_Splice_Rec_572429,Human_Splice_Rec_572435,Human_Splice_Rec_572461,Human_Splice_Rec_572469,Human_Splice_Rec_572493 73903 RMVar_ID_73903 Human_SNP_ID_190927232 m1A Human chr4 - 78776420 78776420 78776420 CCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCAAGCCTCACATTCCGCGCTCCCCAAGCGCACAGC CCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCATGCCTCACATTCCGCGCTCCCCAAGCGCACAGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:78776370..78776580 26863196 MeRIP-seq:(Medium) rs977560873 Functional Loss SNV dbSNP153 33..33 33 - - - 73904 RMVar_ID_73904 Human_SNP_ID_190927233 m1A Human chr4 - 78776420 78776420 78776420 CCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCAAGCCTCACATTCCGCGCTCCCCAAGCGCACAGC CCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCACGCCTCACATTCCGCGCTCCCCAAGCGCACAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:78776370..78776580 26863196 MeRIP-seq:(Medium) rs977560873 Functional Loss SNV dbSNP153 33..33 33 - - - 73905 RMVar_ID_73905 Human_SNP_ID_190927234 m1A Human chr4 - 78776421 78776421 78776421 CCCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCAAGCCTCACATTCCGCGCTCCCCAAGCGCACAG CCCTGGCCCGTCCGAGCGTGCTGCGGCCCGCCGAGCCTCACATTCCGCGCTCCCCAAGCGCACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:78776374..78776503;chr4:78776373..78776564 26863196 MeRIP-seq:(Medium) rs928852772 Functional Loss SNV dbSNP153 33..33 33 - - - 73906 RMVar_ID_73906 Human_SNP_ID_190966011 m1A Human chr4 - 78939276 78939276 78939276 GGGGCGCCAGCGGCGAAGCCCCCTCCCCGGGGAGGCGGGACCTGGGGGAGCTCCCGAGCCGGGGA GGGGCGCCAGCGGCGAAGCCCCCTCCCCGGGGGGGCGGGACCTGGGGGAGCTCCCGAGCCGGGGA T C PAQR3 Ensembl:ENSG00000163291 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:78939227..78939385 26863196 MeRIP-seq:(Medium) rs1259182558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837561,Human_RBP_ID_4794640,Human_RBP_ID_23034702 RMVar_hsa_circ_89880,RMVar_hsa_circ_226918 73907 RMVar_ID_73907 Human_SNP_ID_191783937 m1A Human chr4 - 82354127 82354127 82354127 TCCAGGTGGTGAAGCAGTATTTTCCAATTTGAAGATTCATTTGAAGGTGGCTCCTGCCACCTGCT TCCAGGTGGTGAAGCAGTATTTTCCAATTTGACGATTCATTTGAAGGTGGCTCCTGCCACCTGCT T G HNRNPD Ensembl:ENSG00000138668 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:82354076..82354193 32194978 MeRIP-seq:(Medium) rs1172767959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72623,Human_RBP_ID_625333,Human_RBP_ID_1640678,Human_RBP_ID_1981382,Human_RBP_ID_15208100,Human_RBP_ID_22679257,Human_RBP_ID_22826521,Human_RBP_ID_24066346,Human_RBP_ID_24430442,Human_RBP_ID_24502012,Human_RBP_ID_24561695,Human_RBP_ID_25829292,Human_RBP_ID_27070592,Human_RBP_ID_27730469 Human_Splice_Rec_573822,Human_Splice_Rec_573838,Human_Splice_Rec_573850,Human_Splice_Rec_573864 RMVar_hsa_circ_226956,RMVar_hsa_circ_226957 73908 RMVar_ID_73908 Human_SNP_ID_191784210 m1A Human chr4 - 82355403 82355403 82355403 TACCGTTCTGGTTCTAACACTTGTTTTATTTTAGACCAGCAGAGTGGTTATGGGAAGGTATCCAG TACCGTTCTGGTTCTAACACTTGTTTTATTTTTGACCAGCAGAGTGGTTATGGGAAGGTATCCAG T A HNRNPD Ensembl:ENSG00000138668 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82355401..82355425 26863196 MeRIP-seq:(Medium) rs771273994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18032403,Human_RBP_ID_19121702,Human_RBP_ID_22458340,Human_RBP_ID_24547881 Human_Splice_Rec_573821,Human_Splice_Rec_573837,Human_Splice_Rec_573847,Human_Splice_Rec_573863 RMVar_hsa_circ_3832,RMVar_hsa_circ_226956,RMVar_hsa_circ_320661,RMVar_hsa_circ_226957,RMVar_hsa_circ_344031,RMVar_hsa_circ_30856,RMVar_hsa_circ_226958 73909 RMVar_ID_73909 Human_SNP_ID_191789618 m1A Human chr4 - 82373602 82373602 82373602 AACGGCGGCGGTAGGCGGCTCGGCGGGCGAGCAGGAGGGAGCCATGGTGGCGGCGACACAGGGGG AACGGCGGCGGTAGGCGGCTCGGCGGGCGAGCGGGAGGGAGCCATGGTGGCGGCGACACAGGGGG T C HNRNPD Ensembl:ENSG00000138668 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:82371562..82373991 26863410 MeRIP-seq:(Medium) rs747503862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162336,Human_RBP_ID_249261,Human_RBP_ID_625367,Human_RBP_ID_786471,Human_RBP_ID_1069392,Human_RBP_ID_3966845,Human_RBP_ID_4791812,Human_RBP_ID_7332017,Human_RBP_ID_15209151,Human_RBP_ID_22533963,Human_RBP_ID_26349416 73910 RMVar_ID_73910 Human_SNP_ID_191789628 m1A Human chr4 + 82373615 82373615 82373615 CGCCACCATGGCTCCCTCCTGCTCGCCCGCCGAGCCGCCTACCGCCGCCGTTGCCGCTGCCGCCG CGCCACCATGGCTCCCTCCTGCTCGCCCGCCGGGCCGCCTACCGCCGCCGTTGCCGCTGCCGCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:82373439..82374000;chr4:82373146..82373975;chr4:82373451..82374000;chr4:82359451..82374468;chr4:82358676..82374453;chr4:82359475..82374353 26863196 MeRIP-seq:(Medium) rs1224237157 Functional Loss SNV dbSNP153 33..33 33 - - - 73911 RMVar_ID_73911 Human_SNP_ID_191789638 m1A Human chr4 - 82373633 82373633 82373633 AGTTCGGCGGGGACGGGGCGGCGGCAGCGGCAACGGCGGCGGTAGGCGGCTCGGCGGGCGAGCAG AGTTCGGCGGGGACGGGGCGGCGGCAGCGGCAGCGGCGGCGGTAGGCGGCTCGGCGGGCGAGCAG T C HNRNPD Ensembl:ENSG00000138668 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr4:82371562..82373741 26863410 MeRIP-seq:(Medium) rs1560442190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162336,Human_RBP_ID_249261,Human_RBP_ID_625367,Human_RBP_ID_1069392,Human_RBP_ID_3966845,Human_RBP_ID_4800832,Human_RBP_ID_7332018,Human_RBP_ID_15209151,Human_RBP_ID_22533963,Human_RBP_ID_26349416 Human_Splice_Rec_573913 73912 RMVar_ID_73912 Human_SNP_ID_191789647 m1A Human chr4 - 82373640 82373640 82373640 GAGGAGCAGTTCGGCGGGGACGGGGCGGCGGCAGCGGCAACGGCGGCGGTAGGCGGCTCGGCGGG GAGGAGCAGTTCGGCGGGGACGGGGCGGCGGCGGCGGCAACGGCGGCGGTAGGCGGCTCGGCGGG T C HNRNPD Ensembl:ENSG00000138668 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:82373426..82374000 26863196 MeRIP-seq:(Medium) rs769991211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162336,Human_RBP_ID_249261,Human_RBP_ID_1069392,Human_RBP_ID_3966845,Human_RBP_ID_4800832,Human_RBP_ID_7332018,Human_RBP_ID_15209151,Human_RBP_ID_17030783,Human_RBP_ID_22533963,Human_RBP_ID_26349416 Human_Splice_Rec_573892,Human_Splice_Rec_573913 73913 RMVar_ID_73913 Human_SNP_ID_191789802 m1A Human chr4 - 82373944 82373941 82373944 TGGTCCGCGGCGGCGCCATTAAAGCGAGGAGGAGGCGAGAGCGGCCGCCGCTGGTGCTTATTCTT TGGTCCGCGGCGGCGCCATTAAAGCGAGGAGG___CGAGAGCGGCCGCCGCTGGTGCTTATTCTT GCCT G HNRNPD Ensembl:ENSG00000138668 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:82373842..82373961 26863410 MeRIP-seq:(Medium) rs1231938982 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_625373,Human_RBP_ID_4795025,Human_RBP_ID_7332028,Human_RBP_ID_22531730,Human_RBP_ID_24066486,Human_RBP_ID_24535824,Human_RBP_ID_26349418,Human_RBP_ID_27070665 73914 RMVar_ID_73914 Human_SNP_ID_191789807 m1A Human chr4 - 82373944 82373944 82373944 TGGTCCGCGGCGGCGCCATTAAAGCGAGGAGGAGGCGAGAGCGGCCGCCGCTGGTGCTTATTCTT TGGTCCGCGGCGGCGCCATTAAAGCGAGGAGGCGGCGAGAGCGGCCGCCGCTGGTGCTTATTCTT T G HNRNPD Ensembl:ENSG00000138668 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:82373842..82373961 26863410 MeRIP-seq:(Medium) rs1381145772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_625373,Human_RBP_ID_4795025,Human_RBP_ID_7332028,Human_RBP_ID_22531730,Human_RBP_ID_24066486,Human_RBP_ID_24535824,Human_RBP_ID_26349418,Human_RBP_ID_27070665 73915 RMVar_ID_73915 Human_SNP_ID_191802971 m1A Human chr4 - 82423591 82423591 82423591 TACGTGTTCACAGGCAGAGTAGTTGATCTCACACAACGGGTGATCTCACAAAACTGGTAAGTTTC TACGTGTTCACAGGCAGAGTAGTTGATCTCACGCAACGGGTGATCTCACAAAACTGGTAAGTTTC T C HNRNPDL Ensembl:ENSG00000152795 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7332076,Human_RBP_ID_15245379,Human_RBP_ID_17296314,Human_RBP_ID_18032409 Human_miRNA_ID_323881 GWAS_ID_8923,GWAS_ID_8924 73916 RMVar_ID_73916 Human_SNP_ID_191803412 m1A Human chr4 - 82424882 82424882 82424882 AATCTAACTGGTATTTTGTTTTTGTTTTTAGGAGGAGATGTTAAAGTAACCCATCTTGCAGGACG AATCTAACTGGTATTTTGTTTTTGTTTTTAGGGGGAGATGTTAAAGTAACCCATCTTGCAGGACG T C HNRNPDL Ensembl:ENSG00000152795 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:82424851..82424900 32194978 MeRIP-seq:(Medium) rs982396700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72766,Human_RBP_ID_625444,Human_RBP_ID_939700,Human_RBP_ID_1640777,Human_RBP_ID_1981508,Human_RBP_ID_3744460,Human_RBP_ID_7332118,Human_RBP_ID_9349183,Human_RBP_ID_15209301,Human_RBP_ID_18826953,Human_RBP_ID_22552621,Human_RBP_ID_22679261,Human_RBP_ID_22745608,Human_RBP_ID_24561698,Human_RBP_ID_25823006,Human_RBP_ID_27841959 Human_Splice_Rec_573934,Human_Splice_Rec_573948,Human_Splice_Rec_573960,Human_Splice_Rec_573986,Human_Splice_Rec_574002,Human_Splice_Rec_574018,Human_Splice_Rec_574036,Human_Splice_Rec_574052 73917 RMVar_ID_73917 Human_SNP_ID_191804066 m1A Human chr4 + 82427242 82427242 82427242 CCACCTCGTCCACCAGCTGCAGCACCTCTTCCACCTTTTTGTTGTTGCTGTTGCTGCCTATATAC CCACCTCGTCCACCAGCTGCAGCACCTCTTCCCCCTTTTTGTTGTTGCTGTTGCTGCCTATATAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82427160..82427259 26863196 MeRIP-seq:(Medium) rs757576538 Functional Loss SNV dbSNP153 33..33 33 - - - 73918 RMVar_ID_73918 Human_SNP_ID_191804926 m1A Human chr4 - 82429347 82429347 82429347 GACCCGGACTGCGCGCCAGCACCCCCCTGCCGACAGCTCCGTCACTATGGAGGATATGAACGAGT GACCCGGACTGCGCGCCAGCACCCCCCTGCCGGCAGCTCCGTCACTATGGAGGATATGAACGAGT T C HNRNPDL Ensembl:ENSG00000152795 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:82429301..82429425 26863196 MeRIP-seq:(Medium) rs769253084 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_72774,Human_RBP_ID_625504,Human_RBP_ID_1037469,Human_RBP_ID_1640853,Human_RBP_ID_1981553,Human_RBP_ID_4791933,Human_RBP_ID_7332192,Human_RBP_ID_9396509,Human_RBP_ID_24066587,Human_RBP_ID_26349439,Human_RBP_ID_26519017,Human_RBP_ID_27824263 Human_Splice_Rec_573921,Human_Splice_Rec_573935,Human_Splice_Rec_573949,Human_Splice_Rec_573961,Human_Splice_Rec_573973,Human_Splice_Rec_573987,Human_Splice_Rec_574003,Human_Splice_Rec_574020,Human_Splice_Rec_574021,Human_Splice_Rec_574038,Human_Splice_Rec_574039,Human_Splice_Rec_574053 RMVar_hsa_circ_9108,RMVar_hsa_circ_55840,RMVar_hsa_circ_10161 73919 RMVar_ID_73919 Human_SNP_ID_191804927 m1A Human chr4 - 82429347 82429347 82429347 GACCCGGACTGCGCGCCAGCACCCCCCTGCCGACAGCTCCGTCACTATGGAGGATATGAACGAGT GACCCGGACTGCGCGCCAGCACCCCCCTGCCGCCAGCTCCGTCACTATGGAGGATATGAACGAGT T G HNRNPDL Ensembl:ENSG00000152795 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:82429301..82429425 26863196 MeRIP-seq:(Medium) rs769253084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72774,Human_RBP_ID_625504,Human_RBP_ID_1037469,Human_RBP_ID_1640853,Human_RBP_ID_1981553,Human_RBP_ID_4791933,Human_RBP_ID_7332192,Human_RBP_ID_9396509,Human_RBP_ID_24066587,Human_RBP_ID_26349439,Human_RBP_ID_26519017,Human_RBP_ID_27824263 Human_Splice_Rec_573921,Human_Splice_Rec_573935,Human_Splice_Rec_573949,Human_Splice_Rec_573961,Human_Splice_Rec_573973,Human_Splice_Rec_573987,Human_Splice_Rec_574003,Human_Splice_Rec_574020,Human_Splice_Rec_574021,Human_Splice_Rec_574038,Human_Splice_Rec_574039,Human_Splice_Rec_574053 RMVar_hsa_circ_9108,RMVar_hsa_circ_55840,RMVar_hsa_circ_10161 73920 RMVar_ID_73920 Human_SNP_ID_191804935 m1A Human chr4 + 82429352 82429352 82429352 TTCATATCCTCCATAGTGACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGC TTCATATCCTCCATAGTGACGGAGCTGTCGGCTGGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:82429301..82429562 32194978 MeRIP-seq:(Medium) rs1560458813 Functional Loss SNV dbSNP153 33..33 33 - - - 73921 RMVar_ID_73921 Human_SNP_ID_191804958 m1A Human chr4 + 82429370 82429370 82429370 ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCCGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:82429251..82429700 26863410 MeRIP-seq:(Medium) rs748859467 Functional Loss SNV dbSNP153 33..33 33 - - - 73922 RMVar_ID_73922 Human_SNP_ID_191804959 m1A Human chr4 + 82429370 82429370 82429370 ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCGGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:82429251..82429700 26863410 MeRIP-seq:(Medium) rs748859467 Functional Loss SNV dbSNP153 33..33 33 - - - 73923 RMVar_ID_73923 Human_SNP_ID_191804960 m1A Human chr4 + 82429370 82429370 82429370 ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG ACGGAGCTGTCGGCAGGGGGGTGCTGGCGCGCTGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:82429251..82429700 26863410 MeRIP-seq:(Medium) rs748859467 Functional Loss SNV dbSNP153 33..33 33 - - - 73924 RMVar_ID_73924 Human_SNP_ID_191804981 m1A Human chr4 + 82429385 82429385 82429385 GGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCGTTGTATGGAGCTGGA GGGGGGTGCTGGCGCGCAGTCCGGGTCGCGGCGGCAGCGGCGGCGGAGCGTTGTATGGAGCTGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:82429212..82429969;chr4:82429226..82429450;chr4:82429251..82429450;chr4:82429219..82429475;chr4:82429206..82429462;chr4:82429203..82429450 26863196 MeRIP-seq:(Medium) rs1340894924 Functional Loss SNV dbSNP153 33..33 33 - - - 73925 RMVar_ID_73925 Human_SNP_ID_191804983 m1A Human chr4 + 82429388 82429388 82429388 GGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCGTTGTATGGAGCTGGATTT GGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCGGCGGCGGCGGAGCGTTGTATGGAGCTGGATTT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:82429293..82429450 26863196 MeRIP-seq:(Medium) rs750185803 Functional Loss SNV dbSNP153 33..33 33 - - - 73926 RMVar_ID_73926 Human_SNP_ID_191805020 m1A Human chr4 - 82429418 82429418 82429418 CGGCGCCCGGATCTCTTCCGCCGCCATTTTAAATCCAGCTCCATACAACGCTCCGCCGCCGCTGC CGGCGCCCGGATCTCTTCCGCCGCCATTTTAAGTCCAGCTCCATACAACGCTCCGCCGCCGCTGC T C HNRNPDL Ensembl:ENSG00000152795 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:82429376..82429450 26863196 MeRIP-seq:(Medium) rs372961029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72774,Human_RBP_ID_1037470,Human_RBP_ID_7332194,Human_RBP_ID_17295479,Human_RBP_ID_17525219,Human_RBP_ID_18030246,Human_RBP_ID_25835987,Human_RBP_ID_26695348,Human_RBP_ID_27730568 73927 RMVar_ID_73927 Human_SNP_ID_191805413 m1A Human chr4 + 82430167 82430152 82430167 CTCTTCCACTGTGACCACGGGCGCGCGGGCCAAGGGGGCGCGGCGGGGCCTCCCGGGCTGATCGG CTCTTCCACTGTGACCAC_______________GGGGGCGCGGCGGGGCCTCCCGGGCTGATCGG CGGGCGCGCGGGCCAA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:82430119..82430408 26863196 MeRIP-seq:(Medium) rs1482643390 Functional Loss DEL dbSNP153 19..33 33 - - - 73928 RMVar_ID_73928 Human_SNP_ID_191805413 m1A Human chr4 + 82430166 82430152 82430167 CCTCTTCCACTGTGACCACGGGCGCGCGGGCCAAGGGGGCGCGGCGGGGCCTCCCGGGCTGATCG CCTCTTCCACTGTGACCAC_______________GGGGGCGCGGCGGGGCCTCCCGGGCTGATCG CGGGCGCGCGGGCCAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82430123..82430401 26863196 MeRIP-seq:(Medium) rs1482643390 Functional Loss DEL dbSNP153 20..34 33 - - - 73929 RMVar_ID_73929 Human_SNP_ID_191805418 m1A Human chr4 + 82430166 82430166 82430166 CCTCTTCCACTGTGACCACGGGCGCGCGGGCCAAGGGGGCGCGGCGGGGCCTCCCGGGCTGATCG CCTCTTCCACTGTGACCACGGGCGCGCGGGCCCAGGGGGCGCGGCGGGGCCTCCCGGGCTGATCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82430123..82430401 26863196 MeRIP-seq:(Medium) rs1225669879 Functional Loss SNV dbSNP153 33..33 33 - - - 73930 RMVar_ID_73930 Human_SNP_ID_191805419 m1A Human chr4 + 82430167 82430167 82430167 CTCTTCCACTGTGACCACGGGCGCGCGGGCCAAGGGGGCGCGGCGGGGCCTCCCGGGCTGATCGG CTCTTCCACTGTGACCACGGGCGCGCGGGCCAGGGGGGCGCGGCGGGGCCTCCCGGGCTGATCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:82430119..82430408 26863196 MeRIP-seq:(Medium) rs1482521451 Functional Loss SNV dbSNP153 33..33 33 - - - 73931 RMVar_ID_73931 Human_SNP_ID_191813329 m1A Human chr4 + 82462626 82462626 82462626 TTCTCCAGACTTGATATGAAGTGTGAGGCTCCACCCCTCCTCCCCCCCTCCCCCAACCCCCGCCC TTCTCCAGACTTGATATGAAGTGTGAGGCTCCCCCCCTCCTCCCCCCCTCCCCCAACCCCCGCCC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:82462601..82462675 26863196 MeRIP-seq:(Medium) rs1289438878 Functional Loss SNV dbSNP153 33..33 33 - - - 73932 RMVar_ID_73932 Human_SNP_ID_191813330 m1A Human chr4 + 82462626 82462626 82462626 TTCTCCAGACTTGATATGAAGTGTGAGGCTCCACCCCTCCTCCCCCCCTCCCCCAACCCCCGCCC TTCTCCAGACTTGATATGAAGTGTGAGGCTCCTCCCCTCCTCCCCCCCTCCCCCAACCCCCGCCC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:82462601..82462675 26863196 MeRIP-seq:(Medium) rs1289438878 Functional Loss SNV dbSNP153 33..33 33 - - - 73933 RMVar_ID_73933 Human_SNP_ID_191813359 m1A Human chr4 - 82462661 82462661 82462661 CTCTTAGCTCCATCTGCTGTATTTGGCGGGCGACGGGGCGGGGGTTGGGGGAGGGGGGGAGGAGG CTCTTAGCTCCATCTGCTGTATTTGGCGGGCGGCGGGGCGGGGGTTGGGGGAGGGGGGGAGGAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:82462601..82462675 26863196 MeRIP-seq:(Medium) rs1165467488 Functional Loss SNV dbSNP153 33..33 33 - - - 73934 RMVar_ID_73934 Human_SNP_ID_191903824 m1A Human chr4 - 82842287 82842287 82842287 ACCAGGCCTCTTCACCTACCTCCAGCCCTGCTACTTCTTTCCCTCCTCCCCCTTCCTCTGGAGCA ACCAGGCCTCTTCACCTACCTCCAGCCCTGCTGCTTCTTTCCCTCCTCCCCCTTCCTCTGGAGCA T C SEC31A Ensembl:ENSG00000138674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82842237..82842432 26863196 MeRIP-seq:(Medium) rs779124032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17295887,Human_RBP_ID_17409281,Human_RBP_ID_17525602,Human_RBP_ID_18955286,Human_RBP_ID_27509662 Human_miRNA_ID_20703,Human_miRNA_ID_495536,Human_miRNA_ID_1478969 RMVar_hsa_circ_35530,RMVar_hsa_circ_90287,RMVar_hsa_circ_125182,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_226987,RMVar_hsa_circ_66157,RMVar_hsa_circ_334451,RMVar_hsa_circ_366391,RMVar_hsa_circ_226991,RMVar_hsa_circ_316543,RMVar_hsa_circ_363782,RMVar_hsa_circ_71226,RMVar_hsa_circ_20979,RMVar_hsa_circ_39618,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_322174,RMVar_hsa_circ_331988,RMVar_hsa_circ_344467,RMVar_hsa_circ_295836,RMVar_hsa_circ_41586,RMVar_hsa_circ_44641,RMVar_hsa_circ_226998,RMVar_hsa_circ_25579,RMVar_hsa_circ_226997,RMVar_hsa_circ_226999 73935 RMVar_ID_73935 Human_SNP_ID_191903836 m1A Human chr4 - 82842322 82842322 82842322 CTATACTGGGCAGTCTCAGCTGTACGCAGCACAGCACCAGGCCTCTTCACCTACCTCCAGCCCTG CTATACTGGGCAGTCTCAGCTGTACGCAGCACGGCACCAGGCCTCTTCACCTACCTCCAGCCCTG T C SEC31A Ensembl:ENSG00000138674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:82842198..82842430 26863196 MeRIP-seq:(Medium) rs1353830173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785980,Human_RBP_ID_15210947,Human_RBP_ID_17295888,Human_RBP_ID_17409281,Human_RBP_ID_17525602,Human_RBP_ID_18955286,Human_RBP_ID_21069694 Human_miRNA_ID_1930802,Human_miRNA_ID_1930803 RMVar_hsa_circ_35530,RMVar_hsa_circ_90287,RMVar_hsa_circ_125182,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_226987,RMVar_hsa_circ_66157,RMVar_hsa_circ_334451,RMVar_hsa_circ_366391,RMVar_hsa_circ_226991,RMVar_hsa_circ_316543,RMVar_hsa_circ_363782,RMVar_hsa_circ_71226,RMVar_hsa_circ_20979,RMVar_hsa_circ_39618,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_322174,RMVar_hsa_circ_331988,RMVar_hsa_circ_344467,RMVar_hsa_circ_295836,RMVar_hsa_circ_41586,RMVar_hsa_circ_44641,RMVar_hsa_circ_226998,RMVar_hsa_circ_25579,RMVar_hsa_circ_226997,RMVar_hsa_circ_226999 73936 RMVar_ID_73936 Human_SNP_ID_191905564 m1A Human chr4 - 82848869 82848869 82848869 TTCCGTACGAGAAACAGCAGCTCCCCAAGGGCAGGCCTGGACCAGTTGCTGGCCACCACCAGATG TTCCGTACGAGAAACAGCAGCTCCCCAAGGGCGGGCCTGGACCAGTTGCTGGCCACCACCAGATG T C SEC31A Ensembl:ENSG00000138674 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:82848801..82851570 32194978 MeRIP-seq:(Medium) rs769024482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71424,Human_RBP_ID_160649,Human_RBP_ID_249006,Human_RBP_ID_785985,Human_RBP_ID_837585,Human_RBP_ID_941607,Human_RBP_ID_9397256,Human_RBP_ID_17295895,Human_RBP_ID_17409287,Human_RBP_ID_17525605,Human_RBP_ID_22458343,Human_RBP_ID_26350157 Human_Splice_Rec_574219,Human_Splice_Rec_574281,Human_Splice_Rec_574329,Human_Splice_Rec_574377,Human_Splice_Rec_574429,Human_Splice_Rec_574479,Human_Splice_Rec_574529,Human_Splice_Rec_574579,Human_Splice_Rec_574627,Human_Splice_Rec_574677,Human_Splice_Rec_574733,Human_Splice_Rec_574773,Human_Splice_Rec_574825,Human_Splice_Rec_574839,Human_Splice_Rec_574897 Human_miRNA_ID_462415,Human_miRNA_ID_884482,Human_miRNA_ID_929045,Human_miRNA_ID_1724804,Human_miRNA_ID_1799233,Human_miRNA_ID_2920255,Human_miRNA_ID_2920256 RMVar_hsa_circ_90287,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_334451,RMVar_hsa_circ_366391,RMVar_hsa_circ_226991,RMVar_hsa_circ_316543,RMVar_hsa_circ_363782,RMVar_hsa_circ_71226,RMVar_hsa_circ_20979,RMVar_hsa_circ_39618,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_322174,RMVar_hsa_circ_331988,RMVar_hsa_circ_295836,RMVar_hsa_circ_41586,RMVar_hsa_circ_44641,RMVar_hsa_circ_226998,RMVar_hsa_circ_226997,RMVar_hsa_circ_227000,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_331560,RMVar_hsa_circ_304268,RMVar_hsa_circ_22264,RMVar_hsa_circ_23583,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227001,RMVar_hsa_circ_38343,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_351886,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004 73937 RMVar_ID_73937 Human_SNP_ID_191912495 m1A Human chr4 + 82875820 82875820 82875820 TCAGATTCATTAGCACCAGAAGCTACCAGATTAGTCTGCAAGAAGAAACCATAACTAAATAGCAC TCAGATTCATTAGCACCAGAAGCTACCAGATTGGTCTGCAAGAAGAAACCATAACTAAATAGCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:82875778..82877526 32194978 MeRIP-seq:(Medium) rs1393157287 Functional Loss SNV dbSNP153 33..33 33 - - - 73938 RMVar_ID_73938 Human_SNP_ID_191913776 m1A Human chr4 - 82880907 82880907 82880907 AAATATATTTTCTATAGGAACATCTGCTCAGCAATTGGATGCAACATTTAGTACGAATGCTTCCC AAATATATTTTCTATAGGAACATCTGCTCAGCGATTGGATGCAACATTTAGTACGAATGCTTCCC T C SEC31A Ensembl:ENSG00000138674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82880858..82880971 26863196 MeRIP-seq:(Medium) rs1275750611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71457,Human_RBP_ID_310764,Human_RBP_ID_941632,Human_RBP_ID_3966867,Human_RBP_ID_17295904 Human_Splice_Rec_574184,Human_Splice_Rec_574250,Human_Splice_Rec_574298,Human_Splice_Rec_574342,Human_Splice_Rec_574394,Human_Splice_Rec_574444,Human_Splice_Rec_574494,Human_Splice_Rec_574544,Human_Splice_Rec_574596,Human_Splice_Rec_574642,Human_Splice_Rec_574698,Human_Splice_Rec_574794,Human_Splice_Rec_574862,Human_Splice_Rec_574954,Human_Splice_Rec_574986,Human_Splice_Rec_574996,Human_Splice_Rec_575004,Human_Splice_Rec_575012,Human_Splice_Rec_575020,Human_Splice_Rec_575028,Human_Splice_Rec_575036,Human_Splice_Rec_575044,Human_Splice_Rec_575056,Human_Splice_Rec_575062,Human_Splice_Rec_575068 Human_miRNA_ID_2580612,Human_miRNA_ID_2580613,Human_miRNA_ID_2580614 RMVar_hsa_circ_37,RMVar_hsa_circ_90287,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_334451,RMVar_hsa_circ_226991,RMVar_hsa_circ_316543,RMVar_hsa_circ_71226,RMVar_hsa_circ_66854,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_226998,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_367722,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_374948,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_69666,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_26026,RMVar_hsa_circ_25009,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_94343,RMVar_hsa_circ_227030,RMVar_hsa_circ_325320,RMVar_hsa_circ_227027,RMVar_hsa_circ_327116,RMVar_hsa_circ_294248,RMVar_hsa_circ_227028,RMVar_hsa_circ_227029,RMVar_hsa_circ_373786,RMVar_hsa_circ_374445,RMVar_hsa_circ_313179,RMVar_hsa_circ_95034,RMVar_hsa_circ_227034,RMVar_hsa_circ_227035,RMVar_hsa_circ_227036,RMVar_hsa_circ_227033,RMVar_hsa_circ_227038,RMVar_hsa_circ_104688,RMVar_hsa_circ_277826,RMVar_hsa_circ_304963,RMVar_hsa_circ_316751,RMVar_hsa_circ_227040,RMVar_hsa_circ_227039,RMVar_hsa_circ_277391,RMVar_hsa_circ_227037,RMVar_hsa_circ_281739,RMVar_hsa_circ_270333,RMVar_hsa_circ_227042,RMVar_hsa_circ_227043,RMVar_hsa_circ_227044,RMVar_hsa_circ_315616,RMVar_hsa_circ_281832,RMVar_hsa_circ_43137,RMVar_hsa_circ_370194,RMVar_hsa_circ_227045,RMVar_hsa_circ_227046 73939 RMVar_ID_73939 Human_SNP_ID_191914064 m1A Human chr4 - 82881917 82881917 82881917 TCCCTTTAGCAGGATGAAGTTAAAGGAAGTAGATCGTACAGCCATGCAGGCATGGAGCCCTGCCC TCCCTTTAGCAGGATGAAGTTAAAGGAAGTAGGTCGTACAGCCATGCAGGCATGGAGCCCTGCCC T C SEC31A Ensembl:ENSG00000138674 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:82881851..82881950 26863196 MeRIP-seq:(Medium) rs139031667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71458,Human_RBP_ID_941633,Human_RBP_ID_1981612,Human_RBP_ID_4795031,Human_RBP_ID_7332696,Human_RBP_ID_15211401,Human_RBP_ID_23034711,Human_RBP_ID_26350461 Human_Splice_Rec_574182,Human_Splice_Rec_574183,Human_Splice_Rec_574248,Human_Splice_Rec_574249,Human_Splice_Rec_574296,Human_Splice_Rec_574297,Human_Splice_Rec_574392,Human_Splice_Rec_574393,Human_Splice_Rec_574442,Human_Splice_Rec_574443,Human_Splice_Rec_574492,Human_Splice_Rec_574493,Human_Splice_Rec_574543,Human_Splice_Rec_574595,Human_Splice_Rec_574640,Human_Splice_Rec_574641,Human_Splice_Rec_574696,Human_Splice_Rec_574697,Human_Splice_Rec_574792,Human_Splice_Rec_574793,Human_Splice_Rec_574860,Human_Splice_Rec_574861,Human_Splice_Rec_574952,Human_Splice_Rec_574953,Human_Splice_Rec_574974,Human_Splice_Rec_574975,Human_Splice_Rec_574984,Human_Splice_Rec_574985,Human_Splice_Rec_574994,Human_Splice_Rec_574995,Human_Splice_Rec_575002,Human_Splice_Rec_575003,Human_Splice_Rec_575010,Human_Splice_Rec_575011,Human_Splice_Rec_575018,Human_Splice_Rec_575019,Human_Splice_Rec_575026,Human_Splice_Rec_575027,Human_Splice_Rec_575034,Human_Splice_Rec_575035,Human_Splice_Rec_575042,Human_Splice_Rec_575043,Human_Splice_Rec_575054,Human_Splice_Rec_575055,Human_Splice_Rec_575060,Human_Splice_Rec_575061,Human_Splice_Rec_575066,Human_Splice_Rec_575067,Human_Splice_Rec_575074,Human_Splice_Rec_575080 RMVar_hsa_circ_90287,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_334451,RMVar_hsa_circ_226991,RMVar_hsa_circ_316543,RMVar_hsa_circ_71226,RMVar_hsa_circ_66854,RMVar_hsa_circ_331988,RMVar_hsa_circ_309134,RMVar_hsa_circ_367722,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_374948,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_69666,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_26026,RMVar_hsa_circ_25009,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_331490,RMVar_hsa_circ_94343,RMVar_hsa_circ_227027,RMVar_hsa_circ_327116,RMVar_hsa_circ_294248,RMVar_hsa_circ_227028,RMVar_hsa_circ_227029,RMVar_hsa_circ_373786,RMVar_hsa_circ_313179,RMVar_hsa_circ_95034,RMVar_hsa_circ_227034,RMVar_hsa_circ_227035,RMVar_hsa_circ_227036,RMVar_hsa_circ_227038,RMVar_hsa_circ_104688,RMVar_hsa_circ_277826,RMVar_hsa_circ_316751,RMVar_hsa_circ_227039,RMVar_hsa_circ_277391,RMVar_hsa_circ_227037,RMVar_hsa_circ_281739,RMVar_hsa_circ_227043,RMVar_hsa_circ_227044,RMVar_hsa_circ_281832,RMVar_hsa_circ_370194,RMVar_hsa_circ_227045,RMVar_hsa_circ_227046 73940 RMVar_ID_73940 Human_SNP_ID_191916607 m1A Human chr4 - 82891121 82891121 82891121 GAATGCTGGGAGAGTCCGACGAGCGCTGCACTAACGCAGGATCCGGCTGCCGAAGGTCCTCGCCA GAATGCTGGGAGAGTCCGACGAGCGCTGCACTGACGCAGGATCCGGCTGCCGAAGGTCCTCGCCA T C SEC31A Ensembl:ENSG00000138674 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:82890969..82891125 26863196 MeRIP-seq:(Medium) rs766066256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838022,Human_RBP_ID_4795033,Human_RBP_ID_7332727,Human_RBP_ID_23034712 Human_Splice_Rec_574181,Human_Splice_Rec_574247,Human_Splice_Rec_574295,Human_Splice_Rec_574341,Human_Splice_Rec_574391,Human_Splice_Rec_574441,Human_Splice_Rec_574491,Human_Splice_Rec_574639,Human_Splice_Rec_574791,Human_Splice_Rec_574859,Human_Splice_Rec_574951,Human_Splice_Rec_574973,Human_Splice_Rec_574983,Human_Splice_Rec_575009,Human_Splice_Rec_575017,Human_Splice_Rec_575025,Human_Splice_Rec_575033,Human_Splice_Rec_575041 Human_miRNA_ID_1983309 RMVar_hsa_circ_90287,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 73941 RMVar_ID_73941 Human_SNP_ID_191919036 m1A Human chr4 + 82900854 82900854 82900854 CAGTGGGCTGCAGCACCCGTGACACCGTGCTCAGCCGGGAGCGCGGCCTCTCCTTCCACCAGTGC CAGTGGGCTGCAGCACCCGTGACACCGTGCTCTGCCGGGAGCGCGGCCTCTCCTTCCACCAGTGC A T THAP9 Ensembl:ENSG00000168152 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82900807..82900899 26863196 MeRIP-seq:(Medium) rs1309567803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18030353 Human_Splice_Rec_575141,Human_Splice_Rec_575147,Human_Splice_Rec_575153,Human_Splice_Rec_575161,Human_Splice_Rec_575169 73942 RMVar_ID_73942 Human_SNP_ID_191944173 m1A Human chr4 + 83006963 83006963 83006963 GGAGTTTGAGACCAGCCTGGCCAACATGGTCAAACCCCGTCTCTACTAAAAATACAAAAAGTAGC GGAGTTTGAGACCAGCCTGGCCAACATGGTCAGACCCCGTCTCTACTAAAAATACAAAAAGTAGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:83006837..83006966 26863196 MeRIP-seq:(Medium) rs1314094470 Functional Loss SNV dbSNP153 33..33 33 - - - 73943 RMVar_ID_73943 Human_SNP_ID_191945053 m1A Human chr4 + 83010784 83010784 83010784 CATCACCATCACAGCTCAGCAGCTTCCCCGACAGCCGGAGCCCGGGCCGCCGCCGCCGCCGCCAC CATCACCATCACAGCTCAGCAGCTTCCCCGACGGCCGGAGCCCGGGCCGCCGCCGCCGCCGCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:83010690..83010825 26863196 MeRIP-seq:(Medium) rs1004101943 Functional Loss SNV dbSNP153 33..33 33 - - - 73944 RMVar_ID_73944 Human_SNP_ID_191945595 m1A Human chr4 - 83012868 83012868 83012868 TGATTTTGAACAAACCCTGGTCTGTGTCTCGGAGGCGCCGCCGCCGCCGCTGCTGCTGGGAGCCC TGATTTTGAACAAACCCTGGTCTGTGTCTCGGTGGCGCCGCCGCCGCCGCTGCTGCTGGGAGCCC T A LIN54 Ensembl:ENSG00000189308 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:83012743..83012920 26863196 MeRIP-seq:(Medium) rs948679714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940872,Human_RBP_ID_4794651,Human_RBP_ID_5150751,Human_RBP_ID_5395362,Human_RBP_ID_5475858,Human_RBP_ID_9334742,Human_RBP_ID_18424608 Human_Splice_Rec_575287,Human_Splice_Rec_575351,Human_Splice_Rec_575375 73945 RMVar_ID_73945 Human_SNP_ID_191945596 m1A Human chr4 - 83012868 83012868 83012868 TGATTTTGAACAAACCCTGGTCTGTGTCTCGGAGGCGCCGCCGCCGCCGCTGCTGCTGGGAGCCC TGATTTTGAACAAACCCTGGTCTGTGTCTCGGGGGCGCCGCCGCCGCCGCTGCTGCTGGGAGCCC T C LIN54 Ensembl:ENSG00000189308 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:83012743..83012920 26863196 MeRIP-seq:(Medium) rs948679714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940872,Human_RBP_ID_4794651,Human_RBP_ID_5150751,Human_RBP_ID_5395362,Human_RBP_ID_5475858,Human_RBP_ID_9334742,Human_RBP_ID_18424608 Human_Splice_Rec_575287,Human_Splice_Rec_575351,Human_Splice_Rec_575375 73946 RMVar_ID_73946 Human_SNP_ID_191951237 m1A Human chr4 + 83035247 83035247 83035247 TGGGAGAAAGATGGCGGCAGCCGTGCGACAGGATTTGGCCCAGCTCATGAATTCGAGCGGCTCTC TGGGAGAAAGATGGCGGCAGCCGTGCGACAGGGTTTGGCCCAGCTCATGAATTCGAGCGGCTCTC A G COPS4 Ensembl:ENSG00000138663 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:83035161..83035343 26863196 MeRIP-seq:(Medium) rs773327561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_625748,Human_RBP_ID_4795517 Human_Splice_Rec_575379,Human_Splice_Rec_575395,Human_Splice_Rec_575399,Human_Splice_Rec_575411,Human_Splice_Rec_575415,Human_Splice_Rec_575433,Human_Splice_Rec_575441,Human_Splice_Rec_575447,Human_Splice_Rec_575467 73947 RMVar_ID_73947 Human_SNP_ID_191955069 m1A Human chr4 + 83050742 83050742 83050742 AGTGTGGATAGAGTAGAGTGAGCAAAGGGGCAAGAGATCAGGGATGAGAGTAGAGAGTACTGGGG AGTGTGGATAGAGTAGAGTGAGCAAAGGGGCAGGAGATCAGGGATGAGAGTAGAGAGTACTGGGG A G COPS4 Ensembl:ENSG00000138663 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:83050716..83050952 26863196 MeRIP-seq:(Medium) rs1387915845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838076,Human_RBP_ID_7333109,Human_RBP_ID_15213028 RMVar_hsa_circ_3563,RMVar_hsa_circ_18490,RMVar_hsa_circ_313592,RMVar_hsa_circ_276803,RMVar_hsa_circ_300163,RMVar_hsa_circ_347003,RMVar_hsa_circ_88702,RMVar_hsa_circ_227068,RMVar_hsa_circ_227069,RMVar_hsa_circ_227070 73948 RMVar_ID_73948 Human_SNP_ID_191955360 m1A Human chr4 + 83052012 83052012 83052012 TGGTGAGCTATGGCATTGATAGGTCAAGTAAGATAAGGAGTACAGGTTAACTGTTGGCATTAGTA TGGTGAGCTATGGCATTGATAGGTCAAGTAAGTTAAGGAGTACAGGTTAACTGTTGGCATTAGTA A T COPS4 Ensembl:ENSG00000138663 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:83051869..83052257 26863196 MeRIP-seq:(Medium) rs1248646574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3563,RMVar_hsa_circ_18490,RMVar_hsa_circ_313592,RMVar_hsa_circ_276803,RMVar_hsa_circ_300163,RMVar_hsa_circ_347003,RMVar_hsa_circ_88702,RMVar_hsa_circ_227068,RMVar_hsa_circ_227069,RMVar_hsa_circ_227070 73949 RMVar_ID_73949 Human_SNP_ID_192008102 m1A Human chr4 - 83269995 83269992 83269996 GACTTTCCCCCTTTTTGTGTTTTGCTAATTGTAGGCTTGACATTTAATTGGGGAGCGTTACTTGG GACTTTCCCCCTTTTTGTGTTTTGCTAATTG____CTTGACATTTAATTGGGGAGCGTTACTTGG GCCTA G COQ2 Ensembl:ENSG00000173085 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:83269945..83272138 32194978 MeRIP-seq:(Medium) rs937215195 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_76538,RMVar_hsa_circ_227078,RMVar_hsa_circ_366570,RMVar_hsa_circ_227080,RMVar_hsa_circ_227079,RMVar_hsa_circ_282552,RMVar_hsa_circ_285614,RMVar_hsa_circ_227081 73950 RMVar_ID_73950 Human_SNP_ID_192011608 m1A Human chr4 - 83284550 83284550 83284550 GGCGGTGGTGGACTCTGCGCCCCGCCCCCTGCAGCCGTACTTGCGCCTCATGCGGTTGGACAAGC GGCGGTGGTGGACTCTGCGCCCCGCCCCCTGCCGCCGTACTTGCGCCTCATGCGGTTGGACAAGC T G COQ2 Ensembl:ENSG00000173085 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:83284444..83284570 26863196 MeRIP-seq:(Medium) rs759389317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795519 Human_Splice_Rec_575547,Human_Splice_Rec_575571,Human_Splice_Rec_575583,Human_Splice_Rec_575595 73951 RMVar_ID_73951 Human_SNP_ID_192023456 m1A Human chr4 + 83334656 83334656 83334656 GCTCACCAGGTGCAGCGGCTCCTGGGTGAAGAAGTCCAGGTCCACGACGTCCTGTGCTTGCGCAG GCTCACCAGGTGCAGCGGCTCCTGGGTGAAGAGGTCCAGGTCCACGACGTCCTGTGCTTGCGCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:83334585..83334740 26863196 MeRIP-seq:(Medium) rs1036336506 Functional Loss SNV dbSNP153 33..33 33 - - - 73952 RMVar_ID_73952 Human_SNP_ID_192023457 m1A Human chr4 + 83334661 83334661 83334661 CCAGGTGCAGCGGCTCCTGGGTGAAGAAGTCCAGGTCCACGACGTCCTGTGCTTGCGCAGGTCGG CCAGGTGCAGCGGCTCCTGGGTGAAGAAGTCCCGGTCCACGACGTCCTGTGCTTGCGCAGGTCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:83334612..83334818;chr4:83334610..83334815 26863196 MeRIP-seq:(Medium) rs759295404 Functional Loss SNV dbSNP153 33..33 33 - - - 73953 RMVar_ID_73953 Human_SNP_ID_192023458 m1A Human chr4 + 83334661 83334661 83334661 CCAGGTGCAGCGGCTCCTGGGTGAAGAAGTCCAGGTCCACGACGTCCTGTGCTTGCGCAGGTCGG CCAGGTGCAGCGGCTCCTGGGTGAAGAAGTCCGGGTCCACGACGTCCTGTGCTTGCGCAGGTCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:83334612..83334818;chr4:83334610..83334815 26863196 MeRIP-seq:(Medium) rs759295404 Functional Loss SNV dbSNP153 33..33 33 - - - 73954 RMVar_ID_73954 Human_SNP_ID_192053835 m1A Human chr4 + 83456120 83456120 83456120 TGGTTGCTGTTTGCGGTGGTCTAGGGAGGAAGAAGTTGACACACTTGGTAACGGCTGCTGTCAGC TGGTTGCTGTTTGCGGTGGTCTAGGGAGGAAGTAGTTGACACACTTGGTAACGGCTGCTGTCAGC A T MRPS18C Ensembl:ENSG00000163319 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:83455986..83456141 26863196 MeRIP-seq:(Medium) rs779366652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838075,Human_RBP_ID_4795038,Human_RBP_ID_18413481,Human_RBP_ID_19014507,Human_RBP_ID_23213814,Human_RBP_ID_24554257,Human_RBP_ID_26349445 Human_Splice_Rec_575869,Human_Splice_Rec_575871,Human_Splice_Rec_575879,Human_Splice_Rec_575885,Human_Splice_Rec_575895,Human_Splice_Rec_575905 RMVar_hsa_circ_97304,RMVar_hsa_circ_227105 73955 RMVar_ID_73955 Human_SNP_ID_192299238 m1A Human chr4 + 84492889 84492889 84492889 TCGCTCCGAGGTCCCCCATGCGGTGAGCGTGAACCCTTCCACAGCACCTCTCGGCGCCCCCTACC TCGCTCCGAGGTCCCCCATGCGGTGAGCGTGACCCCTTCCACAGCACCTCTCGGCGCCCCCTACC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:84492841..84492955 32194978 MeRIP-seq:(Medium) rs1394721013 Functional Loss SNV dbSNP153 33..33 33 - - - 73956 RMVar_ID_73956 Human_SNP_ID_192411167 m1A Human chr4 - 84958781 84958776 84958782 CTGAAGCAGGGTGCTTGGCACATTCACAGAACAGTAAGGGGTTGGCTGGAAGGAGGTGAACCATG CTGAAGCAGGGTGCTTGGCACATTCACAGAA______GGGGTTGGCTGGAAGGAGGTGAACCATG CTTACTG C WDFY3 Ensembl:ENSG00000163625 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:84958774..84958853 26863196 MeRIP-seq:(Medium) rs1310628799 Functional Loss DEL dbSNP153 32..37 33 - - - 73957 RMVar_ID_73957 Human_SNP_ID_192413201 m1A Human chr4 - 84966513 84966513 84966513 GGAGCGCCGAGGCTGAGGCGGCGGCGGCGGGGACCCAGCGAGGACGAGGACGCGGCGGAGCAGGG GGAGCGCCGAGGCTGAGGCGGCGGCGGCGGGGGCCCAGCGAGGACGAGGACGCGGCGGAGCAGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:84966463..84966650 26863196 MeRIP-seq:(Medium) rs1457030362 Functional Loss SNV dbSNP153 33..33 33 - - - 73958 RMVar_ID_73958 Human_SNP_ID_192413239 m1A Human chr4 - 84966618 84966618 84966618 GGATTAAAGATGGCCACCAACAGCTGCGGGAAACGGCAACAACCCCTCACTTTCCGGGATGGTCC GGATTAAAGATGGCCACCAACAGCTGCGGGAAGCGGCAACAACCCCTCACTTTCCGGGATGGTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:84966445..84966721;chr4:84966426..84966730 26863196 MeRIP-seq:(Medium) rs1394868454 Functional Loss SNV dbSNP153 33..33 33 - - - 73959 RMVar_ID_73959 Human_SNP_ID_192655667 m1A Human chr4 + 85995065 85995065 85995065 GAAGGAGCTCTTCACTGAAGGTATCTGGTACCAAAATGGGCACGCACAGTGTACAGAATGGAACG GAAGGAGCTCTTCACTGAAGGTATCTGGTACCGAAATGGGCACGCACAGTGTACAGAATGGAACG A G ARHGAP24 Ensembl:ENSG00000138639 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:85994956..85995074 32194978 MeRIP-seq:(Medium) rs1257715362 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8925,GWAS_ID_8926,GWAS_ID_8927 RMVar_hsa_circ_43718,RMVar_hsa_circ_49161,RMVar_hsa_circ_367233 73960 RMVar_ID_73960 Human_SNP_ID_192793242 m1A Human chr4 - 86594385 86594385 86594385 GCGGACCGGGGAGCTACGGAGCACGGCTCGCCAGCACGACGGTCTCCAGGGGCCGTGAGCATGGT GCGGACCGGGGAGCTACGGAGCACGGCTCGCCTGCACGACGGTCTCCAGGGGCCGTGAGCATGGT T A MAPK10 Ensembl:ENSG00000109339 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:86594334..86594419 26863196 MeRIP-seq:(Medium) rs1467975139 Functional Loss SNV dbSNP153 33..33 33 - - - 73961 RMVar_ID_73961 Human_SNP_ID_192793327 m1A Human chr4 - 86594668 86594668 86594668 CGGGCGCCGAGAGCCACCACCACTTCTCCCACAAGCGGCTGCGGGCGTGGGCTGAAGGAGCTGTA CGGGCGCCGAGAGCCACCACCACTTCTCCCACGAGCGGCTGCGGGCGTGGGCTGAAGGAGCTGTA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:86594544..86594671 26863196 MeRIP-seq:(Medium) rs1278838759 Functional Loss SNV dbSNP153 33..33 33 - - - 73962 RMVar_ID_73962 Human_SNP_ID_192884549 m1A Human chr4 + 86976063 86976063 86976063 GAAGTGTAAATGTAAATGAATGGTTATAATACAGTGTGTTAAGTTCAATGATGGAGGGATGTAAC GAAGTGTAAATGTAAATGAATGGTTATAATACTGTGTGTTAAGTTCAATGATGGAGGGATGTAAC A T AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:86976036..86976187 26863196 MeRIP-seq:(Medium) rs891429322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5211447 RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 73963 RMVar_ID_73963 Human_SNP_ID_192891725 m1A Human chr4 + 86999875 86999875 86999875 AAGGAGACTGGGTGGTAGCGTTTACAGAGAAGAAACCAATGTATTGGGAGAAATGCCTTGTGCTG AAGGAGACTGGGTGGTAGCGTTTACAGAGAAGGAACCAATGTATTGGGAGAAATGCCTTGTGCTG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:86999827..86999934 26863196 MeRIP-seq:(Medium) rs1299888744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 73964 RMVar_ID_73964 Human_SNP_ID_192897728 m1A Human chr4 - 87021232 87021232 87021232 GTAATCCATTTAAAACTTTAGTACTTCTGAAAAACAGGATGAGGTTTTACAAATTTGTTAGGAAG GTAATCCATTTAAAACTTTAGTACTTCTGAAAGACAGGATGAGGTTTTACAAATTTGTTAGGAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:87021229..87021377 26863196 MeRIP-seq:(Medium) rs968471185 Functional Loss SNV dbSNP153 33..33 33 - - - 73965 RMVar_ID_73965 Human_SNP_ID_192905127 m1A Human chr4 + 87047416 87047416 87047416 TCCCTCCCTCCCCTCAAAAAGTGTTGCAATGCAGCAGAAGCCCACGGCTTATGTCCGGCCCATGG TCCCTCCCTCCCCTCAAAAAGTGTTGCAATGCCGCAGAAGCCCACGGCTTATGTCCGGCCCATGG A C AFF1 Ensembl:ENSG00000172493 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:87047367..87047470 26863196 MeRIP-seq:(Medium) rs200946563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72117,Human_RBP_ID_9397281,Human_RBP_ID_17409300,Human_RBP_ID_18955646 Human_miRNA_ID_2445089,Human_miRNA_ID_2445090,Human_miRNA_ID_2445091,Human_miRNA_ID_2446475,Human_miRNA_ID_2446476,Human_miRNA_ID_2446477 RMVar_hsa_circ_74967,RMVar_hsa_circ_119225,RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450,RMVar_hsa_circ_124989,RMVar_hsa_circ_336477,RMVar_hsa_circ_227320,RMVar_hsa_circ_115837,RMVar_hsa_circ_227321,RMVar_hsa_circ_227319,RMVar_hsa_circ_374834,RMVar_hsa_circ_281625,RMVar_hsa_circ_317354,RMVar_hsa_circ_279818,RMVar_hsa_circ_86046,RMVar_hsa_circ_227323,RMVar_hsa_circ_56109,RMVar_hsa_circ_227324,RMVar_hsa_circ_227322,RMVar_hsa_circ_369947,RMVar_hsa_circ_227325,RMVar_hsa_circ_227326 73966 RMVar_ID_73966 Human_SNP_ID_192905128 m1A Human chr4 + 87047416 87047416 87047416 TCCCTCCCTCCCCTCAAAAAGTGTTGCAATGCAGCAGAAGCCCACGGCTTATGTCCGGCCCATGG TCCCTCCCTCCCCTCAAAAAGTGTTGCAATGCTGCAGAAGCCCACGGCTTATGTCCGGCCCATGG A T AFF1 Ensembl:ENSG00000172493 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:87047367..87047470 26863196 MeRIP-seq:(Medium) rs200946563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72117,Human_RBP_ID_9397281,Human_RBP_ID_17409300,Human_RBP_ID_18955646 Human_miRNA_ID_2445089,Human_miRNA_ID_2445090,Human_miRNA_ID_2445091,Human_miRNA_ID_2446475,Human_miRNA_ID_2446476,Human_miRNA_ID_2446477 RMVar_hsa_circ_74967,RMVar_hsa_circ_119225,RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450,RMVar_hsa_circ_124989,RMVar_hsa_circ_336477,RMVar_hsa_circ_227320,RMVar_hsa_circ_115837,RMVar_hsa_circ_227321,RMVar_hsa_circ_227319,RMVar_hsa_circ_374834,RMVar_hsa_circ_281625,RMVar_hsa_circ_317354,RMVar_hsa_circ_279818,RMVar_hsa_circ_86046,RMVar_hsa_circ_227323,RMVar_hsa_circ_56109,RMVar_hsa_circ_227324,RMVar_hsa_circ_227322,RMVar_hsa_circ_369947,RMVar_hsa_circ_227325,RMVar_hsa_circ_227326 73967 RMVar_ID_73967 Human_SNP_ID_192906720 m1A Human chr4 - 87052743 87052743 87052743 GTACATGGCTACTATCCACATACATGGCTACTACCCCAAGCCACTATCATTTCCTATCTCCCAAC GTACATGGCTACTATCCACATACATGGCTACTCCCCCAAGCCACTATCATTTCCTATCTCCCAAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:87052726..87052811 26863196 MeRIP-seq:(Medium) rs928613280 Functional Loss SNV dbSNP153 33..33 33 - - - 73968 RMVar_ID_73968 Human_SNP_ID_192918936 m1A Human chr4 + 87097682 87097682 87097682 GGTAAGAGTAACACAGAAGAGAAGTGATACTGAGGCCGAGTAGATAATGAGGGTTGTGTGGACTT GGTAAGAGTAACACAGAAGAGAAGTGATACTGGGGCCGAGTAGATAATGAGGGTTGTGTGGACTT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:87097632..87097729 26863196 MeRIP-seq:(Medium) rs540024654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74967,RMVar_hsa_circ_119225,RMVar_hsa_circ_365059,RMVar_hsa_circ_227319,RMVar_hsa_circ_374834,RMVar_hsa_circ_227324,RMVar_hsa_circ_41929,RMVar_hsa_circ_117842,RMVar_hsa_circ_14666,RMVar_hsa_circ_227329,RMVar_hsa_circ_227330,RMVar_hsa_circ_350325,RMVar_hsa_circ_369159,RMVar_hsa_circ_109186,RMVar_hsa_circ_331147,RMVar_hsa_circ_366737 73969 RMVar_ID_73969 Human_SNP_ID_192923404 m1A Human chr4 + 87114865 87114865 87114865 AGCCAGCAGTGCCCCCCTCCAGTGAGAAGAAGAAGCACAAGAGCTCCCTCCCTGCCCCCTCTAAG AGCCAGCAGTGCCCCCCTCCAGTGAGAAGAAGCAGCACAAGAGCTCCCTCCCTGCCCCCTCTAAG A C AFF1 Ensembl:ENSG00000172493 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:87114814..87114930 26863196 MeRIP-seq:(Medium) rs200738066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941945,Human_RBP_ID_5210531,Human_RBP_ID_24561760,Human_RBP_ID_27824279 Human_miRNA_ID_1367046,Human_miRNA_ID_2236348,Human_miRNA_ID_2236349,Human_miRNA_ID_2689091,Human_miRNA_ID_2689092,Human_miRNA_ID_2692275,Human_miRNA_ID_2692276 RMVar_hsa_circ_4679,RMVar_hsa_circ_74967,RMVar_hsa_circ_365059,RMVar_hsa_circ_374834,RMVar_hsa_circ_227324,RMVar_hsa_circ_41929,RMVar_hsa_circ_117842,RMVar_hsa_circ_227329,RMVar_hsa_circ_227330,RMVar_hsa_circ_350325,RMVar_hsa_circ_109186,RMVar_hsa_circ_366737,RMVar_hsa_circ_296368,RMVar_hsa_circ_20399,RMVar_hsa_circ_340552,RMVar_hsa_circ_360241,RMVar_hsa_circ_363755,RMVar_hsa_circ_284703,RMVar_hsa_circ_267231,RMVar_hsa_circ_227332 73970 RMVar_ID_73970 Human_SNP_ID_192926230 m1A Human chr4 + 87125086 87125086 87125086 CTGTGATAACAAGAAAATCAGACTGGAGAAGGAAATCAAATCACAGTCATCTTCATCTTCATCCT CTGTGATAACAAGAAAATCAGACTGGAGAAGGGAATCAAATCACAGTCATCTTCATCTTCATCCT A G AFF1 Ensembl:ENSG00000172493 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:87124976..87125092 26863196 MeRIP-seq:(Medium) rs1251771720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2863107,Human_RBP_ID_18031088,Human_RBP_ID_18537072 Human_Splice_Rec_580986,Human_Splice_Rec_580987,Human_Splice_Rec_581038,Human_Splice_Rec_581039,Human_Splice_Rec_581096,Human_Splice_Rec_581097,Human_Splice_Rec_581148,Human_Splice_Rec_581149,Human_Splice_Rec_581180 RMVar_hsa_circ_4679,RMVar_hsa_circ_74967,RMVar_hsa_circ_117842,RMVar_hsa_circ_227329,RMVar_hsa_circ_227330,RMVar_hsa_circ_109186,RMVar_hsa_circ_65143,RMVar_hsa_circ_20399,RMVar_hsa_circ_360241,RMVar_hsa_circ_363755,RMVar_hsa_circ_267231 73971 RMVar_ID_73971 Human_SNP_ID_192949805 m1A Human chr4 + 87220498 87220498 87220498 GTTACCACGCTCCCAGAGCCCCGGCCGCCCTCAGCGGAACCTCACCAACCCCGCGCGAGCACCCG GTTACCACGCTCCCAGAGCCCCGGCCGCCCTCCGCGGAACCTCACCAACCCCGCGCGAGCACCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:87220449..87220546 26863196 MeRIP-seq:(Medium) rs1168926860 Functional Loss SNV dbSNP153 33..33 33 - - - 73972 RMVar_ID_73972 Human_SNP_ID_193113161 m1A Human chr4 - 87892490 87892490 87892490 ATCACTAATTTCCTTGTCTTGTTCCTTCTCCAAATAAAGGGTGATGGGATAGCCTATGAACTGAG ATCACTAATTTCCTTGTCTTGTTCCTTCTCCAGATAAAGGGTGATGGGATAGCCTATGAACTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:87892434..87892600;chr4:87892434..87892650;chr4:87892426..87892647 26863196 MeRIP-seq:(Medium) rs780432275 Functional Loss SNV dbSNP153 33..33 33 - - - 73973 RMVar_ID_73973 Human_SNP_ID_193113162 m1A Human chr4 - 87892490 87892490 87892490 ATCACTAATTTCCTTGTCTTGTTCCTTCTCCAAATAAAGGGTGATGGGATAGCCTATGAACTGAG ATCACTAATTTCCTTGTCTTGTTCCTTCTCCACATAAAGGGTGATGGGATAGCCTATGAACTGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:87892434..87892600;chr4:87892434..87892650;chr4:87892426..87892647 26863196 MeRIP-seq:(Medium) rs780432275 Functional Loss SNV dbSNP153 33..33 33 - - - 73974 RMVar_ID_73974 Human_SNP_ID_193141407 m1A Human chr4 + 88008184 88008184 88008184 GGCTTGGGGGCTACCACGGCGCGGGCCACCCGAGCGGGAGGCGGCGCCGGCGAGAGGACCAGGGC GGCTTGGGGGCTACCACGGCGCGGGCCACCCGGGCGGGAGGCGGCGCCGGCGAGAGGACCAGGGC A G PKD2 Ensembl:ENSG00000118762 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:88007658..88019497 26863196 MeRIP-seq:(Medium) rs1391653115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150995 RMVar_hsa_circ_227363,RMVar_hsa_circ_88796,RMVar_hsa_circ_101960,RMVar_hsa_circ_227364 73975 RMVar_ID_73975 Human_SNP_ID_193177654 m1A Human chr4 - 88158550 88158550 88158550 AACTGGGTAGGATTTAGGAACGCACCGTGCACATGCTTGGTGGTCTTGTTAAGTGGAAACTGCTG AACTGGGTAGGATTTAGGAACGCACCGTGCACGTGCTTGGTGGTCTTGTTAAGTGGAAACTGCTG T C ABCG2 Ensembl:ENSG00000118777 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:88158526..88158656 26863196 MeRIP-seq:(Medium) rs754682253 Functional Loss SNV dbSNP153 33..33 33 - - - 73976 RMVar_ID_73976 Human_SNP_ID_193177655 m1A Human chr4 - 88158550 88158550 88158550 AACTGGGTAGGATTTAGGAACGCACCGTGCACATGCTTGGTGGTCTTGTTAAGTGGAAACTGCTG AACTGGGTAGGATTTAGGAACGCACCGTGCACCTGCTTGGTGGTCTTGTTAAGTGGAAACTGCTG T G ABCG2 Ensembl:ENSG00000118777 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:88158526..88158656 26863196 MeRIP-seq:(Medium) rs754682253 Functional Loss SNV dbSNP153 33..33 33 - - - 73977 RMVar_ID_73977 Human_SNP_ID_193203377 m1A Human chr4 + 88266820 88266820 88266820 GATGCTGGATGACTGGGTGCAGGTGATGCTAGATGACTGGGTGCAGGCGATGTTGGCTGATTGGG GATGCTGGATGACTGGGTGCAGGTGATGCTAGCTGACTGGGTGCAGGCGATGTTGGCTGATTGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:88266774..88266868 26863196 MeRIP-seq:(Medium) rs1283402565 Functional Loss SNV dbSNP153 33..33 33 - - - 73978 RMVar_ID_73978 Human_SNP_ID_193265087 m1A Human chr4 - 88523725 88523725 88523725 GGAGCTCGGCCACGGGTGGCGAGGCTGCGGTGAGGCCTGGTCTCCGGCTGCCAGACCATGCTGAG GGAGCTCGGCCACGGGTGGCGAGGCTGCGGTGTGGCCTGGTCTCCGGCTGCCAGACCATGCTGAG T A PYURF Ensembl:ENSG00000145337 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:88523518..88523775 26863196 MeRIP-seq:(Medium) rs998015853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249447,Human_RBP_ID_626395,Human_RBP_ID_4794663,Human_RBP_ID_24069387 73979 RMVar_ID_73979 Human_SNP_ID_193280346 m1A Human chr4 - 88592253 88592253 88592253 GGTGACAGGACTCGAGGGCCCGGCGCGGGGACAGCGGCACGGGTGTGTCAGCCGAAATCGGACTG GGTGACAGGACTCGAGGGCCCGGCGCGGGGACCGCGGCACGGGTGTGTCAGCCGAAATCGGACTG T G lnc-PYURF-2,lnc-PYURF-2:2,lnc-PYURF-2:3,lnc-PYURF-2:4 RNACentral:URS0000D5ABE9,RNACentral:URS00008BE8B5,RNACentral:URS0000D5983B,RNACentral:URS0000D5DC93 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:88592135..88592298 26863196 MeRIP-seq:(Medium) rs1481112096 Functional Loss SNV dbSNP153 33..33 33 - - - 73980 RMVar_ID_73980 Human_SNP_ID_193280358 m1A Human chr4 - 88592271 88592271 88592271 CAGGCGCAGGCTGCCCGAGGTGACAGGACTCGAGGGCCCGGCGCGGGGACAGCGGCACGGGTGTG CAGGCGCAGGCTGCCCGAGGTGACAGGACTCGTGGGCCCGGCGCGGGGACAGCGGCACGGGTGTG T A lnc-PYURF-2,lnc-PYURF-2:2,lnc-PYURF-2:3,lnc-PYURF-2:4 RNACentral:URS0000D5ABE9,RNACentral:URS00008BE8B5,RNACentral:URS0000D5983B,RNACentral:URS0000D5DC93 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:88592014..88592279 26863196 MeRIP-seq:(Medium) rs969614424 Functional Loss SNV dbSNP153 33..33 33 - - - 73981 RMVar_ID_73981 Human_SNP_ID_193402416 m1A Human chr4 - 89111619 89111619 89111619 CAGACCACACTAAGCGCAAATGGAGTCTCCTGAGGCAGGCTGGCACTGGTGGCCCGGCAGCGGCG CAGACCACACTAAGCGCAAATGGAGTCTCCTGGGGCAGGCTGGCACTGGTGGCCCGGCAGCGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:89111570..89111715 26863196 MeRIP-seq:(Medium) rs1323114372 Functional Loss SNV dbSNP153 33..33 33 - - - 73982 RMVar_ID_73982 Human_SNP_ID_193580849 m1A Human chr4 + 89837085 89837085 89837085 TCTCGGAGGGGCCGGGCCGGGGTCTGCGCTGCAGCCCGCACGCACCTCACTTCCGCGTCGCGGCG TCTCGGAGGGGCCGGGCCGGGGTCTGCGCTGCCGCCCGCACGCACCTCACTTCCGCGTCGCGGCG A C SNCA-AS1 Ensembl:ENSG00000247775 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:89836994..89837193 26863410 MeRIP-seq:(Medium) rs1039568907 Functional Loss SNV dbSNP153 33..33 33 - - - 73983 RMVar_ID_73983 Human_SNP_ID_89291885 m1A Human chr2 + 120177264 120177264 120177264 TCTCTTGAGAAGAGAGAGGCATGTGTGCCGGCATCCTTGATGGGTTCAAAGAGAAAGGTTGGAGA TCTCTTGAGAAGAGAGAGGCATGTGTGCCGGCCTCCTTGATGGGTTCAAAGAGAAAGGTTGGAGA A C EPB41L5 Ensembl:ENSG00000115109 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:120177216..120177419 26863196 MeRIP-seq:(Medium) rs113822748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202927,RMVar_hsa_circ_109642,RMVar_hsa_circ_267256 73984 RMVar_ID_73984 Human_SNP_ID_89310278 m1A Human chr2 - 120252901 120252901 120252901 CTTAAACGCGCCCCGCCCCCTCCCGGGGCCGGACCCCAGCCGTCCTCCACCGATTTGTCATTGAG CTTAAACGCGCCCCGCCCCCTCCCGGGGCCGGGCCCCAGCCGTCCTCCACCGATTTGTCATTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:120252777..120253030;chr2:120252788..120253310;chr2:120252779..120253360;chr2:120252851..120252999 26863196 MeRIP-seq:(Medium) rs1558945028 Functional Loss SNV dbSNP153 33..33 33 - - - 73985 RMVar_ID_73985 Human_SNP_ID_89312455 m1A Human chr2 + 120261347 120261347 120261347 TGGTGGAGGGCTTGGCCTTTGCTAAGAGCAGGAATGTGTACTCCATGAGGCTGGAGACAAGGAGA TGGTGGAGGGCTTGGCCTTTGCTAAGAGCAGGCATGTGTACTCCATGAGGCTGGAGACAAGGAGA A C RALB Ensembl:ENSG00000144118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120261343..120261426 26863196 MeRIP-seq:(Medium) rs562303928 Functional Loss SNV dbSNP153 33..33 33 - - - 73986 RMVar_ID_73986 Human_SNP_ID_89316708 m1A Human chr2 - 120278060 120278036 120278060 GCCCACATTCACACACATGCTCACACTCACACACGCTCACATTCACACACACTCACGCTCTCACA GCCCACATTCACACACATGCTCACACTCACAC________________________GCTCTCACA CGTGAGTGTGTGTGAATGTGAGCGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:120278056..120278149 26863196 MeRIP-seq:(Medium) rs1238896637 Functional Loss DEL dbSNP153 33..56 33 - - - 73987 RMVar_ID_73987 Human_SNP_ID_89316882 m1A Human chr2 - 120278566 120278566 120278566 AGACTTAGAGGCGATTTGCTTTCAACCTAGCTAAAACCAAATGTCATTCACATCCTCCATTAAAG AGACTTAGAGGCGATTTGCTTTCAACCTAGCTGAAACCAAATGTCATTCACATCCTCCATTAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120278563..120278737 26863196 MeRIP-seq:(Medium) rs1282807231 Functional Loss SNV dbSNP153 33..33 33 - - - 73988 RMVar_ID_73988 Human_SNP_ID_89319673 m1A Human chr2 - 120289669 120289668 120289669 CTTCGGCTTTACTCCTGGCCTCCTCCACAGGCACCTGCCTCCGCTCCTCTAGGTCAGACTTGTTT CTTCGGCTTTACTCCTGGCCTCCTCCACAGGC_CCTGCCTCCGCTCCTCTAGGTCAGACTTGTTT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:120289620..120293182 26863196 MeRIP-seq:(Medium) rs1382527096 Functional Loss DEL dbSNP153 33..33 33 - - - 73989 RMVar_ID_73989 Human_SNP_ID_89320485 m1A Human chr2 + 120293231 120293231 120293231 AGAATGGCAAGAAAAGCAGCAAGAACAAGAAAAGTTTTAAAGAAAGATGTTGCTTACTATGAGTG AGAATGGCAAGAAAAGCAGCAAGAACAAGAAAGGTTTTAAAGAAAGATGTTGCTTACTATGAGTG A G RALB Ensembl:ENSG00000144118 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:120293181..120293528 32194978 MeRIP-seq:(Medium) rs756077966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23821512 Human_Splice_Rec_292640,Human_Splice_Rec_292650,Human_Splice_Rec_292658,Human_Splice_Rec_292670 RMVar_hsa_circ_82602,RMVar_hsa_circ_202952 73990 RMVar_ID_73990 Human_SNP_ID_89320796 m1A Human chr2 + 120294692 120294692 120294692 CTCCCAAAGAATCATGGGCTTTTTTTTTGAATAAAAAAGCAGACAAATAGACTTTCTCGGGATTT CTCCCAAAGAATCATGGGCTTTTTTTTTGAATTAAAAAGCAGACAAATAGACTTTCTCGGGATTT A T RALB Ensembl:ENSG00000144118 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_533343,Human_RBP_ID_26656792 Human_miRNA_ID_835021 GWAS_ID_8928 RMVar_hsa_circ_82602,RMVar_hsa_circ_202952 73991 RMVar_ID_73991 Human_SNP_ID_89333977 m1A Human chr2 + 120345328 120345328 120345328 CGGCGCCCCGCGCCCGGCCGGGCCGCGCAGGCAGGCGGAGGGAAGGAGGGAGGCTGCGAGGAGGC CGGCGCCCCGCGCCCGGCCGGGCCGCGCAGGCGGGCGGAGGGAAGGAGGGAGGCTGCGAGGAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:120345278..120345440 32194978 MeRIP-seq:(Medium) rs1458091377 Functional Loss SNV dbSNP153 33..33 33 - - - 73992 RMVar_ID_73992 Human_SNP_ID_89334097 m1A Human chr2 + 120345719 120345719 120345719 AAGCCGCGCCCGGCTCCGCTCCGGGGGGCTCCAGCGCCTTCGCTTCCGTCTCAGCCAAGTTGCGT AAGCCGCGCCCGGCTCCGCTCCGGGGGGCTCCGGCGCCTTCGCTTCCGTCTCAGCCAAGTTGCGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:120345594..120345740 32194978 MeRIP-seq:(Medium) rs1029026938 Functional Loss SNV dbSNP153 33..33 33 - - - 73993 RMVar_ID_73993 Human_SNP_ID_89334167 m1A Human chr2 - 120345904 120345904 120345904 CGGGCGGGGCGGAGGTCGCGGGTCACTGCCGCACGGGCGTCTCGGGGCGCCTCGGCATCTGCAGC CGGGCGGGGCGGAGGTCGCGGGTCACTGCCGCGCGGGCGTCTCGGGGCGCCTCGGCATCTGCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120345866..120345989 26863196 MeRIP-seq:(Medium) rs1477645336 Functional Loss SNV dbSNP153 33..33 33 - - - 73994 RMVar_ID_73994 Human_SNP_ID_89334168 m1A Human chr2 - 120345904 120345904 120345904 CGGGCGGGGCGGAGGTCGCGGGTCACTGCCGCACGGGCGTCTCGGGGCGCCTCGGCATCTGCAGC CGGGCGGGGCGGAGGTCGCGGGTCACTGCCGCCCGGGCGTCTCGGGGCGCCTCGGCATCTGCAGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120345866..120345989 26863196 MeRIP-seq:(Medium) rs1477645336 Functional Loss SNV dbSNP153 33..33 33 - - - 73995 RMVar_ID_73995 Human_SNP_ID_89434773 m1A Human chr2 + 120735999 120735999 120735999 GGCGGCGGCGGCGGCTGCGACTGCGAACGCGGAGGAAGGCCAGGAGCCGCAGGAGGAGCCGGAGG GGCGGCGGCGGCGGCTGCGACTGCGAACGCGGGGGAAGGCCAGGAGCCGCAGGAGGAGCCGGAGG A G GLI2 Ensembl:ENSG00000074047 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:120735921..120736028 26863196 MeRIP-seq:(Medium) rs1041923718 Functional Loss SNV dbSNP153 33..33 33 - - - 73996 RMVar_ID_73996 Human_SNP_ID_89441842 m1A Human chr2 - 120766133 120766133 120766133 CATGCTGAAGAACAGCAGGGATAACTCATCCCAGCCCCAGCCTTGCCGCGTGAACCTCCGAACCC CATGCTGAAGAACAGCAGGGATAACTCATCCCTGCCCCAGCCTTGCCGCGTGAACCTCCGAACCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:120766124..120766224 32194978 MeRIP-seq:(Medium) rs192733545 Functional Loss SNV dbSNP153 33..33 33 - - - 73997 RMVar_ID_73997 Human_SNP_ID_89453039 m1A Human chr2 + 120811519 120811519 120811519 CTTAAAGAATGAGAGAGCTACTGGGAAGGTGGAGGTGAGCAGAGGCTCAACGAGGGGTGGATGAC CTTAAAGAATGAGAGAGCTACTGGGAAGGTGGGGGTGAGCAGAGGCTCAACGAGGGGTGGATGAC A G GLI2 Ensembl:ENSG00000074047 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120811470..120811677 26863196 MeRIP-seq:(Medium) rs1338890715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49555 73998 RMVar_ID_73998 Human_SNP_ID_89461849 m1A Human chr2 + 120848185 120848185 120848185 TGAATGCCTCTGGCTTCTGAACTTGAGAAGGAAGCTCCCGGGATGGGCCTGACTCCGCCGCCTGG TGAATGCCTCTGGCTTCTGAACTTGAGAAGGAGGCTCCCGGGATGGGCCTGACTCCGCCGCCTGG A G GLI2 Ensembl:ENSG00000074047 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:120848183..120848317 32194978 MeRIP-seq:(Medium) rs888782546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49555 73999 RMVar_ID_73999 Human_SNP_ID_89462977 m1A Human chr2 + 120852857 120852857 120852857 CAGCCAGCACTCGCTGTGCCCAGTGTGTGGCCACTGTGATGGTTCTGGGTGTGTGAAGAGGGTCA CAGCCAGCACTCGCTGTGCCCAGTGTGTGGCCCCTGTGATGGTTCTGGGTGTGTGAAGAGGGTCA A C GLI2 Ensembl:ENSG00000074047 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:120852852..120852964 32194978 MeRIP-seq:(Medium) rs928960046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49555 74000 RMVar_ID_74000 Human_SNP_ID_89492733 m1A Human chr2 + 120970532 120970532 120970532 AGCCCTCACCCACCTTCCTGGCCCAGCAGCCCATGGCCCTCACCTCCATCAATGCCACGCCCACC AGCCCTCACCCACCTTCCTGGCCCAGCAGCCCCTGGCCCTCACCTCCATCAATGCCACGCCCACC A C GLI2 Ensembl:ENSG00000074047 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:120970356..120970542 26863196 MeRIP-seq:(Medium) rs377150486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_292737,Human_Splice_Rec_292757,Human_Splice_Rec_292777,Human_Splice_Rec_292795,Human_Splice_Rec_292821,Human_Splice_Rec_292837,Human_Splice_Rec_292861,Human_Splice_Rec_292885,Human_Splice_Rec_292911 74001 RMVar_ID_74001 Human_SNP_ID_89492734 m1A Human chr2 + 120970532 120970532 120970532 AGCCCTCACCCACCTTCCTGGCCCAGCAGCCCATGGCCCTCACCTCCATCAATGCCACGCCCACC AGCCCTCACCCACCTTCCTGGCCCAGCAGCCCGTGGCCCTCACCTCCATCAATGCCACGCCCACC A G GLI2 Ensembl:ENSG00000074047 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:120970356..120970542 26863196 MeRIP-seq:(Medium) rs377150486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_292737,Human_Splice_Rec_292757,Human_Splice_Rec_292777,Human_Splice_Rec_292795,Human_Splice_Rec_292821,Human_Splice_Rec_292837,Human_Splice_Rec_292861,Human_Splice_Rec_292885,Human_Splice_Rec_292911 74002 RMVar_ID_74002 Human_SNP_ID_89519653 m1A Human chr2 + 121075265 121075265 121075265 GCTCCTGCCATCTGCCATGAGTTATAGAAAACAGGCAGTGATTAATCAGCCAGTCAACGCCGCGT GCTCCTGCCATCTGCCATGAGTTATAGAAAACCGGCAGTGATTAATCAGCCAGTCAACGCCGCGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:121075164..121075314 26863196 MeRIP-seq:(Medium) rs1486327434 Functional Loss SNV dbSNP153 33..33 33 - - - 74003 RMVar_ID_74003 Human_SNP_ID_89519672 m1A Human chr2 + 121075277 121075277 121075277 TGCCATGAGTTATAGAAAACAGGCAGTGATTAATCAGCCAGTCAACGCCGCGTGCAGCTATCCTC TGCCATGAGTTATAGAAAACAGGCAGTGATTACTCAGCCAGTCAACGCCGCGTGCAGCTATCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:121075226..121075307 26863196 MeRIP-seq:(Medium) rs1055374465 Functional Loss SNV dbSNP153 33..33 33 - - - 74004 RMVar_ID_74004 Human_SNP_ID_89519731 m1A Human chr2 - 121075328 121075326 121075328 CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCAGGGGGCAGATAAATGAAAGAGGATAGCTGCAC CCTATTGCTGCGTGGACTGTGCTGGGGGGGTC__GGGGCAGATAAATGAAAGAGGATAGCTGCAC CCT C lnc-TFCP2L1-6,lnc-TFCP2L1-6:2 RNACentral:URS0000D5E3CC,RNACentral:URS0000D5BAFD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121075215..121075361 26863196 MeRIP-seq:(Medium) rs1199971450 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5500760,Human_RBP_ID_8500110,Human_RBP_ID_27282165 74005 RMVar_ID_74005 Human_SNP_ID_89519732 m1A Human chr2 - 121075328 121075327 121075328 CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCAGGGGGCAGATAAATGAAAGAGGATAGCTGCAC CCTATTGCTGCGTGGACTGTGCTGGGGGGGTC_GGGGGCAGATAAATGAAAGAGGATAGCTGCAC CT C lnc-TFCP2L1-6,lnc-TFCP2L1-6:2 RNACentral:URS0000D5E3CC,RNACentral:URS0000D5BAFD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121075215..121075361 26863196 MeRIP-seq:(Medium) rs1234632677 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5500760,Human_RBP_ID_8500110,Human_RBP_ID_27282165 74006 RMVar_ID_74006 Human_SNP_ID_89519734 m1A Human chr2 - 121075328 121075328 121075328 CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCAGGGGGCAGATAAATGAAAGAGGATAGCTGCAC CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCGGGGGGCAGATAAATGAAAGAGGATAGCTGCAC T C lnc-TFCP2L1-6,lnc-TFCP2L1-6:2 RNACentral:URS0000D5E3CC,RNACentral:URS0000D5BAFD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121075215..121075361 26863196 MeRIP-seq:(Medium) rs1273719968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5500760,Human_RBP_ID_8500110,Human_RBP_ID_27282165 74007 RMVar_ID_74007 Human_SNP_ID_89519735 m1A Human chr2 - 121075328 121075328 121075328 CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCAGGGGGCAGATAAATGAAAGAGGATAGCTGCAC CCTATTGCTGCGTGGACTGTGCTGGGGGGGTCCGGGGGCAGATAAATGAAAGAGGATAGCTGCAC T G lnc-TFCP2L1-6,lnc-TFCP2L1-6:2 RNACentral:URS0000D5E3CC,RNACentral:URS0000D5BAFD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121075215..121075361 26863196 MeRIP-seq:(Medium) rs1273719968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5500760,Human_RBP_ID_8500110,Human_RBP_ID_27282165 74008 RMVar_ID_74008 Human_SNP_ID_89587508 m1A Human chr2 + 121338564 121338563 121338564 GCAAGGCAAGGCAGCTGCAGCTGTCAGGGTCTAGGGGGCGACGGTGGGCTCGGCGCCCTCCCAGT GCAAGGCAAGGCAGCTGCAGCTGTCAGGGTCT_GGGGGCGACGGTGGGCTCGGCGCCCTCCCAGT TA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:121338517..121338659 26863196 MeRIP-seq:(Medium) rs772486510 Functional Loss DEL dbSNP153 33..33 33 - - - 74009 RMVar_ID_74009 Human_SNP_ID_89587517 m1A Human chr2 - 121338581 121338581 121338581 CATGCCGCCACCACCTCACTGGGAGGGCGCCGAGCCCACCGTCGCCCCCTAGACCCTGACAGCTG CATGCCGCCACCACCTCACTGGGAGGGCGCCGGGCCCACCGTCGCCCCCTAGACCCTGACAGCTG T C CLASP1 Ensembl:ENSG00000074054 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121338537..121338664 26863196 MeRIP-seq:(Medium) rs1033774891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_209909,Human_miRNA_ID_1230193 74010 RMVar_ID_74010 Human_SNP_ID_89620728 m1A Human chr2 + 121478731 121478729 121478731 CCACACCCCACACACACAACCACACACACACCACACACACACCCCACACACACCACACACACACC CCACACCCCACACACACAACCACACACACAC__CACACACACCCCACACACACCACACACACACC CCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:121478604..121478769 26863196 MeRIP-seq:(Medium) rs770847103 Functional Loss DEL dbSNP153 32..33 33 - - - 74011 RMVar_ID_74011 Human_SNP_ID_89620729 m1A Human chr2 + 121478731 121478731 121478731 CCACACCCCACACACACAACCACACACACACCACACACACACCCCACACACACCACACACACACC CCACACCCCACACACACAACCACACACACACCCCACACACACCCCACACACACCACACACACACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:121478604..121478769 26863196 MeRIP-seq:(Medium) rs1260955429 Functional Loss SNV dbSNP153 33..33 33 - - - 74012 RMVar_ID_74012 Human_SNP_ID_89620953 m1A Human chr2 + 121478934 121478924 121478935 ACACCACACACACCACACACACACCACACAACACCCCCCACACACACACCACACACACACACCAC ACACCACACACACCACACACACA___________CCCCCACACACACACCACACACACACACCAC ACCACACAACAC A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:121478809..121478940 26863196 MeRIP-seq:(Medium) rs1168094878 Functional Loss DEL dbSNP153 24..34 33 - - - 74013 RMVar_ID_74013 Human_SNP_ID_89633794 m1A Human chr2 + 121530463 121530461 121530463 GAGAGTCCAGACGCATGCCGACTGGAGGACCAAAGAGATTAGCACGAAGAAGGATGATCTTCCAC GAGAGTCCAGACGCATGCCGACTGGAGGACC__AGAGATTAGCACGAAGAAGGATGATCTTCCAC CAA C AC012447.1 Ensembl:ENSG00000265451 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:121530454..121530578 26863196 MeRIP-seq:(Medium) rs1350667588 Functional Loss DEL dbSNP153 32..33 33 - - - 74014 RMVar_ID_74014 Human_SNP_ID_89663183 m1A Human chr2 - 121648869 121648869 121648869 CGGGCGGCCCGGGCTCCCGTCCTGGGCTCCCAACCGGGCCAGACAAAAGCTGCGCGAGCGGCGCC CGGGCGGCCCGGGCTCCCGTCCTGGGCTCCCAGCCGGGCCAGACAAAAGCTGCGCGAGCGGCGCC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:121648863..121648957 26863196 MeRIP-seq:(Medium) rs1559873410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26786592 RMVar_hsa_circ_120025,RMVar_hsa_circ_203015 74015 RMVar_ID_74015 Human_SNP_ID_89689474 m1A Human chr2 + 121755752 121755752 121755752 GCGGCGTCCACTTCCTTGGCCGCCCTTGCTACACTGGCTGATTGTTGTGCAGCCGGCGCCATGTC GCGGCGTCCACTTCCTTGGCCGCCCTTGCTACGCTGGCTGATTGTTGTGCAGCCGGCGCCATGTC A G TSN Ensembl:ENSG00000211460 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:121755701..121755803 26863196 MeRIP-seq:(Medium) rs144025870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_533440,Human_RBP_ID_1577408,Human_RBP_ID_4579886,Human_RBP_ID_5445272,Human_RBP_ID_8852098,Human_RBP_ID_9296801,Human_RBP_ID_9330644,Human_RBP_ID_13597179,Human_RBP_ID_17697135,Human_RBP_ID_17965509,Human_RBP_ID_22452449,Human_RBP_ID_22813462,Human_RBP_ID_23822600 Human_miRNA_ID_2174418,Human_miRNA_ID_2177862 RMVar_hsa_circ_95341,RMVar_hsa_circ_203023 74016 RMVar_ID_74016 Human_SNP_ID_91042463 m1A Human chr2 + 127050493 127050493 127050493 TCACCAGCCTTGAGCTGCAGCTCGTCTGTGTCAGTGGCCGTGTAGTCGTGCTGGGCCTGTACCTG TCACCAGCCTTGAGCTGCAGCTCGTCTGTGTCGGTGGCCGTGTAGTCGTGCTGGGCCTGTACCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127050401..127050525 26863196 MeRIP-seq:(Medium) rs1235145798 Functional Loss SNV dbSNP153 33..33 33 - - - 74017 RMVar_ID_74017 Human_SNP_ID_91044265 m1A Human chr2 + 127056386 127056386 127056386 CCGCGCCTGCCAGGCCCCTGAACTAGGGCGTCACCCACCCAGACACCTGCAGCCTCAGTTCCTTA CCGCGCCTGCCAGGCCCCTGAACTAGGGCGTCGCCCACCCAGACACCTGCAGCCTCAGTTCCTTA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:127056344..127056502 26863196 MeRIP-seq:(Medium) rs1472620754 Functional Loss SNV dbSNP153 33..33 33 - - - 74018 RMVar_ID_74018 Human_SNP_ID_91045025 m1A Human chr2 - 127059046 127059046 127059046 TCAACCACGAGCCAGAGCCGGCCGGCGGGGCCACGCCCGGGGCCACCCTCCCCAAGTCCCCATCT TCAACCACGAGCCAGAGCCGGCCGGCGGGGCCTCGCCCGGGGCCACCCTCCCCAAGTCCCCATCT T A BIN1 Ensembl:ENSG00000136717 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:127059001..127059050 26863196 MeRIP-seq:(Medium) rs753614814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5195510 Human_Splice_Rec_294127,Human_Splice_Rec_294153,Human_Splice_Rec_294185,Human_Splice_Rec_294213,Human_Splice_Rec_294239,Human_Splice_Rec_294267,Human_Splice_Rec_294297,Human_Splice_Rec_294327,Human_Splice_Rec_294357,Human_Splice_Rec_294385,Human_Splice_Rec_294427,Human_Splice_Rec_294443,Human_Splice_Rec_294457 RMVar_hsa_circ_6651,RMVar_hsa_circ_32813,RMVar_hsa_circ_361378 74019 RMVar_ID_74019 Human_SNP_ID_91045954 m1A Human chr2 - 127062190 127062190 127062190 CACCTCCTCACTGTCTCTCCTGCAGCTCAACCAGAACCTCAATGATGTGCTGGTCGGCCTGGAGA CACCTCCTCACTGTCTCTCCTGCAGCTCAACCGGAACCTCAATGATGTGCTGGTCGGCCTGGAGA T C BIN1 Ensembl:ENSG00000136717 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:127062141..127064075 26863196 MeRIP-seq:(Medium) rs751638145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18745436 Human_Splice_Rec_294122,Human_Splice_Rec_294123,Human_Splice_Rec_294150,Human_Splice_Rec_294151,Human_Splice_Rec_294182,Human_Splice_Rec_294183,Human_Splice_Rec_294210,Human_Splice_Rec_294211,Human_Splice_Rec_294234,Human_Splice_Rec_294235,Human_Splice_Rec_294264,Human_Splice_Rec_294265,Human_Splice_Rec_294294,Human_Splice_Rec_294295,Human_Splice_Rec_294324,Human_Splice_Rec_294325,Human_Splice_Rec_294352,Human_Splice_Rec_294353,Human_Splice_Rec_294382,Human_Splice_Rec_294383,Human_Splice_Rec_294424,Human_Splice_Rec_294425,Human_Splice_Rec_294440,Human_Splice_Rec_294441,Human_Splice_Rec_294454,Human_Splice_Rec_294455 RMVar_hsa_circ_104254,RMVar_hsa_circ_6651,RMVar_hsa_circ_361378,RMVar_hsa_circ_114322,RMVar_hsa_circ_203049,RMVar_hsa_circ_93857,RMVar_hsa_circ_203050,RMVar_hsa_circ_203048 74020 RMVar_ID_74020 Human_SNP_ID_91045958 m1A Human chr2 - 127062193 127062193 127062193 CCCCACCTCCTCACTGTCTCTCCTGCAGCTCAACCAGAACCTCAATGATGTGCTGGTCGGCCTGG CCCCACCTCCTCACTGTCTCTCCTGCAGCTCAGCCAGAACCTCAATGATGTGCTGGTCGGCCTGG T C BIN1 Ensembl:ENSG00000136717 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127062101..127062200 26863196 MeRIP-seq:(Medium) rs1184217056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_294122,Human_Splice_Rec_294123,Human_Splice_Rec_294150,Human_Splice_Rec_294151,Human_Splice_Rec_294182,Human_Splice_Rec_294183,Human_Splice_Rec_294210,Human_Splice_Rec_294211,Human_Splice_Rec_294234,Human_Splice_Rec_294235,Human_Splice_Rec_294264,Human_Splice_Rec_294265,Human_Splice_Rec_294294,Human_Splice_Rec_294295,Human_Splice_Rec_294324,Human_Splice_Rec_294325,Human_Splice_Rec_294352,Human_Splice_Rec_294353,Human_Splice_Rec_294382,Human_Splice_Rec_294383,Human_Splice_Rec_294424,Human_Splice_Rec_294425,Human_Splice_Rec_294440,Human_Splice_Rec_294441,Human_Splice_Rec_294454,Human_Splice_Rec_294455 RMVar_hsa_circ_104254,RMVar_hsa_circ_6651,RMVar_hsa_circ_361378,RMVar_hsa_circ_114322,RMVar_hsa_circ_203049,RMVar_hsa_circ_93857,RMVar_hsa_circ_203050,RMVar_hsa_circ_203048 74021 RMVar_ID_74021 Human_SNP_ID_91047759 m1A Human chr2 + 127068974 127068974 127068974 ATCCTTCTTTTTGGCAGTTTGAAGGGACTCGTAGTGGTGCCGGGCACTGTCGTAGTCCACCAGCT ATCCTTCTTTTTGGCAGTTTGAAGGGACTCGTGGTGGTGCCGGGCACTGTCGTAGTCCACCAGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127068879..127068982 26863196 MeRIP-seq:(Medium) rs1553466026 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_339 74022 RMVar_ID_74022 Human_SNP_ID_91085883 m1A Human chr2 + 127218956 127218956 127218956 TGGGAAGGACAGCACTCAGGCTCCAAGTGGGAAGCGTGCGGAATTCGCCGGCCCCAACGCCCTAG TGGGAAGGACAGCACTCAGGCTCCAAGTGGGAGGCGTGCGGAATTCGCCGGCCCCAACGCCCTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127218944..127219081 26863196 MeRIP-seq:(Medium) rs952851926 Functional Loss SNV dbSNP153 33..33 33 - - - 74023 RMVar_ID_74023 Human_SNP_ID_91085991 m1A Human chr2 - 127219392 127219392 127219392 AACCTGGGGAGGGGGCGCCGCGAAGGGAAACCAGGAATGGGACTGCGGGGAGGGCACCAGGGCTG AACCTGGGGAGGGGGCGCCGCGAAGGGAAACCGGGAATGGGACTGCGGGGAGGGCACCAGGGCTG T C CYP27C1 Ensembl:ENSG00000186684 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:127219243..127219815 26863196 MeRIP-seq:(Medium) rs921496506 Functional Loss SNV dbSNP153 33..33 33 - - - 74024 RMVar_ID_74024 Human_SNP_ID_91085992 m1A Human chr2 - 127219392 127219392 127219392 AACCTGGGGAGGGGGCGCCGCGAAGGGAAACCAGGAATGGGACTGCGGGGAGGGCACCAGGGCTG AACCTGGGGAGGGGGCGCCGCGAAGGGAAACCCGGAATGGGACTGCGGGGAGGGCACCAGGGCTG T G CYP27C1 Ensembl:ENSG00000186684 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:127219243..127219815 26863196 MeRIP-seq:(Medium) rs921496506 Functional Loss SNV dbSNP153 33..33 33 - - - 74025 RMVar_ID_74025 Human_SNP_ID_91086210 m1A Human chr2 + 127220209 127220209 127220209 GTTGAGGCCGCCGCGGGGCCCCGCCGCCCAGGAGCCCACCCCGCTCGGGCGCCGGCCGCAGCCCG GTTGAGGCCGCCGCGGGGCCCCGCCGCCCAGGGGCCCACCCCGCTCGGGCGCCGGCCGCAGCCCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:127220160..127220293 26863196 MeRIP-seq:(Medium) rs1404149045 Functional Loss SNV dbSNP153 33..33 33 - - - 74026 RMVar_ID_74026 Human_SNP_ID_91103728 m1A Human chr2 - 127293704 127293704 127293704 TGTGTTGGTATCTTGCAGACAAGAAGAAATCCAGGAAGCGGCACTATGAGGATGAAGAGGATGAT TGTGTTGGTATCTTGCAGACAAGAAGAAATCCTGGAAGCGGCACTATGAGGATGAAGAGGATGAT T A ERCC3 Ensembl:ENSG00000163161 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127293601..127293750 26863196 MeRIP-seq:(Medium) rs1454594744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243847,Human_RBP_ID_777319,Human_RBP_ID_3958227,Human_RBP_ID_9384657,Human_RBP_ID_19002433,Human_RBP_ID_22997448,Human_RBP_ID_24546508,Human_RBP_ID_26339813 Human_Splice_Rec_294530,Human_Splice_Rec_294556,Human_Splice_Rec_294582,Human_Splice_Rec_294618,Human_Splice_Rec_294644,Human_Splice_Rec_294672,Human_Splice_Rec_294718,Human_Splice_Rec_294746,Human_Splice_Rec_294786,Human_Splice_Rec_294808,Human_Splice_Rec_294818,Human_Splice_Rec_294822 RMVar_hsa_circ_51035,RMVar_hsa_circ_203057,RMVar_hsa_circ_335117,RMVar_hsa_circ_203062,RMVar_hsa_circ_304714,RMVar_hsa_circ_305275,RMVar_hsa_circ_203065,RMVar_hsa_circ_301574,RMVar_hsa_circ_332193,RMVar_hsa_circ_339664 74027 RMVar_ID_74027 Human_SNP_ID_91103932 m1A Human chr2 - 127294088 127294088 127294088 TGGGAGCGGGGTCATCTTCTCTCTGCTGCTGTAGCTGCCATGGGCAAAAGAGACCGAGCGGACCG TGGGAGCGGGGTCATCTTCTCTCTGCTGCTGTGGCTGCCATGGGCAAAAGAGACCGAGCGGACCG T C ERCC3 Ensembl:ENSG00000163161 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:127293501..127294150;chr2:127292787..127294150 26863196 MeRIP-seq:(Medium) rs771683547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915782,Human_RBP_ID_1577471,Human_RBP_ID_4623607,Human_RBP_ID_9384658,Human_RBP_ID_19000120 Human_Splice_Rec_294529,Human_Splice_Rec_294581,Human_Splice_Rec_294643,Human_Splice_Rec_294671,Human_Splice_Rec_294717,Human_Splice_Rec_294745,Human_Splice_Rec_294785,Human_Splice_Rec_294807,Human_Splice_Rec_294817,Human_Splice_Rec_294821 74028 RMVar_ID_74028 Human_SNP_ID_91103940 m1A Human chr2 + 127294104 127294104 127294104 TTTTGCCCATGGCAGCTACAGCAGCAGAGAGAAGATGACCCCGCTCCCACAGGCCCGCCGCGGCA TTTTGCCCATGGCAGCTACAGCAGCAGAGAGAGGATGACCCCGCTCCCACAGGCCCGCCGCGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:127294004..127294150;chr2:127293992..127294150 26863196 MeRIP-seq:(Medium) rs1051784504 Functional Loss SNV dbSNP153 33..33 33 - - - 74029 RMVar_ID_74029 Human_SNP_ID_91105917 m1A Human chr2 + 127301624 127301624 127301624 AATACAGATTGTGTTACAAACAAGAAGTCATCAGGCAGAAGGAACAATGGTACTGATTTAATGCC AATACAGATTGTGTTACAAACAAGAAGTCATCCGGCAGAAGGAACAATGGTACTGATTTAATGCC A C AC068282.1 Ensembl:ENSG00000286145 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:127301604..127301719 32194978 MeRIP-seq:(Medium) rs570397299 Functional Loss SNV dbSNP153 33..33 33 - - - 74030 RMVar_ID_74030 Human_SNP_ID_91105918 m1A Human chr2 + 127301624 127301624 127301624 AATACAGATTGTGTTACAAACAAGAAGTCATCAGGCAGAAGGAACAATGGTACTGATTTAATGCC AATACAGATTGTGTTACAAACAAGAAGTCATCGGGCAGAAGGAACAATGGTACTGATTTAATGCC A G AC068282.1 Ensembl:ENSG00000286145 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:127301604..127301719 32194978 MeRIP-seq:(Medium) rs570397299 Functional Loss SNV dbSNP153 33..33 33 - - - 74031 RMVar_ID_74031 Human_SNP_ID_91161910 m1A Human chr2 + 127526343 127526343 127526343 TGCCGCCCGACCGGAGAACTTAACGGGTGCGGAGGGTAAGAAAGCGGTAGCGGCAAAGGCGAATT TGCCGCCCGACCGGAGAACTTAACGGGTGCGGTGGGTAAGAAAGCGGTAGCGGCAAAGGCGAATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:127526292..127526457 26863196 MeRIP-seq:(Medium) rs1396358759 Functional Loss SNV dbSNP153 33..33 33 - - - 74032 RMVar_ID_74032 Human_SNP_ID_91161976 m1A Human chr2 + 127526432 127526432 127526432 AAAGGCCGTACCCGGCAGGCTGGCGGGCGGGCAGGCATGCGAGCCGGCGTTCTACTTCCTAGAAG AAAGGCCGTACCCGGCAGGCTGGCGGGCGGGCGGGCATGCGAGCCGGCGTTCTACTTCCTAGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127526233..127526450 26863196 MeRIP-seq:(Medium) rs1449323110 Functional Loss SNV dbSNP153 33..33 33 - - - 74033 RMVar_ID_74033 Human_SNP_ID_91187967 m1A Human chr2 - 127627280 127627272 127627280 ACCTGTTGGTGGCCAGACCCATGACCTCTGGGAAAGAGAGTTCCAGCAGCATCTTCTCCTGCTGG ACCTGTTGGTGGCCAGACCCATGACCTCTGGG________TTCCAGCAGCATCTTCTCCTGCTGG ACTCTCTTT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:127627229..127628391 32194978 MeRIP-seq:(Medium) rs1314536781 Functional Loss DEL dbSNP153 33..40 33 - - - 74034 RMVar_ID_74034 Human_SNP_ID_91189638 m1A Human chr2 + 127631676 127631676 127631676 CCCACCCTGGAGCTCACCGACCAGATCTTCACACTGGCCCTGCAGCACCCGGCCCTCCAGGACGA CCCACCCTGGAGCTCACCGACCAGATCTTCACGCTGGCCCTGCAGCACCCGGCCCTCCAGGACGA A G MYO7B Ensembl:ENSG00000169994 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:127631247..127632326 32194978 MeRIP-seq:(Medium) rs753818080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_295347,Human_Splice_Rec_295433,Human_Splice_Rec_295483,Human_Splice_Rec_295519,Human_Splice_Rec_295559 RMVar_hsa_circ_266354 74035 RMVar_ID_74035 Human_SNP_ID_91192276 m1A Human chr2 - 127638562 127638562 127638562 CTTGTGTCGAGCCCTTGGGTGGGGCCAGGAGGAGGTGATGGCGTCAGAGGAGGTGTGGTCAGAGG CTTGTGTCGAGCCCTTGGGTGGGGCCAGGAGGTGGTGATGGCGTCAGAGGAGGTGTGGTCAGAGG T A LIMS2 Ensembl:ENSG00000072163 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:127638511..127638620 32194978 MeRIP-seq:(Medium) rs1262764098 Functional Loss SNV dbSNP153 33..33 33 - - - 74036 RMVar_ID_74036 Human_SNP_ID_91196216 m1A Human chr2 - 127651040 127651040 127651040 GGTAGAAGAGGAAGCCGGTGAGACGGCATGCGATTTCCCCAAATGGCCAGTGGTTCCCAGAGAAG GGTAGAAGAGGAAGCCGGTGAGACGGCATGCGGTTTCCCCAAATGGCCAGTGGTTCCCAGAGAAG T C LIMS2 Ensembl:ENSG00000072163 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127651035..127651119 26863196 MeRIP-seq:(Medium) rs1329413553 Functional Loss SNV dbSNP153 33..33 33 - - - 74037 RMVar_ID_74037 Human_SNP_ID_91196224 m1A Human chr2 + 127651054 127651054 127651054 ACTGGCCATTTGGGGAAATCGCATGCCGTCTCACCGGCTTCCTCTTCTACCTCAACATGTACGCC ACTGGCCATTTGGGGAAATCGCATGCCGTCTCGCCGGCTTCCTCTTCTACCTCAACATGTACGCC A G GPR17 Ensembl:ENSG00000144230 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:127651006..127651551 32194978 MeRIP-seq:(Medium) rs781690937 Functional Loss SNV dbSNP153 33..33 33 - - - 74038 RMVar_ID_74038 Human_SNP_ID_91203503 m1A Human chr2 - 127675766 127675766 127675766 TGGACTCGGCGGTCCCGGGTGCCTCGGGAGGGAGTCAGTGCCCAGATCCGCGGTGGGAACTCCGG TGGACTCGGCGGTCCCGGGTGCCTCGGGAGGGGGTCAGTGCCCAGATCCGCGGTGGGAACTCCGG T C LIMS2 Ensembl:ENSG00000072163 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127675679..127675773 26863196 MeRIP-seq:(Medium) rs1233698151 Functional Loss SNV dbSNP153 33..33 33 - - - 74039 RMVar_ID_74039 Human_SNP_ID_91209848 m1A Human chr2 + 127701599 127701591 127701599 GCAGGGGAAAGCTGGCGGCCCGGCGGCCGCGGAGCCGCTGCTCGCCGCGGAGAAGGCGGAGGAGC GCAGGGGAAAGCTGGCGGCCCGGCG________GCCGCTGCTCGCCGCGGAGAAGGCGGAGGAGC GGCCGCGGA G SFT2D3 Ensembl:ENSG00000173349 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:127701552..127701755;chr2:127701551..127701819 26863196 MeRIP-seq:(Medium) rs1170024065 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_533700,Human_RBP_ID_4624719 74040 RMVar_ID_74040 Human_SNP_ID_91209892 m1A Human chr2 + 127701653 127701653 127701653 GGCGGAGGAGCCCGGGGACCGGCCGGCGGAGGAGTGGCTGGGCCGCGCGGGCTTGCGCTGGACGT GGCGGAGGAGCCCGGGGACCGGCCGGCGGAGGGGTGGCTGGGCCGCGCGGGCTTGCGCTGGACGT A G SFT2D3 Ensembl:ENSG00000173349 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:127701557..127701657 26863410 MeRIP-seq:(Medium) rs1202955832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243954,Human_RBP_ID_4622669,Human_RBP_ID_17939256,Human_RBP_ID_22450555 74041 RMVar_ID_74041 Human_SNP_ID_91209971 m1A Human chr2 + 127701792 127701792 127701792 GCGGCGGGCGGCGGGTGCCTGCTGCTGGCTGCACTGTGTTTCGGCCTAGCCGCGCTCTACGCACC GCGGCGGGCGGCGGGTGCCTGCTGCTGGCTGCGCTGTGTTTCGGCCTAGCCGCGCTCTACGCACC A G SFT2D3 Ensembl:ENSG00000173349 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:127701549..127701807 26863410 MeRIP-seq:(Medium) rs753706232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_533701,Human_RBP_ID_27000280 74042 RMVar_ID_74042 Human_SNP_ID_91213398 m1A Human chr2 + 127713662 127713662 127713662 GAAACGTTCATCTCCGGGCCTGCGGCCTTCCCATGCCCCCGGAGGGCCTCGGGCTGCACCCCGGC GAAACGTTCATCTCCGGGCCTGCGGCCTTCCCGTGCCCCCGGAGGGCCTCGGGCTGCACCCCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127713616..127714021 26863196 MeRIP-seq:(Medium) rs754345457 Functional Loss SNV dbSNP153 33..33 33 - - - 74043 RMVar_ID_74043 Human_SNP_ID_91250047 m1A Human chr2 + 127857511 127857511 127857511 AAGATAGGACTCTGTCTCTCTGCCTCTGTGGGAGGGTAGGGGCCTAACTTCGACAGGTGCGCCAG AAGATAGGACTCTGTCTCTCTGCCTCTGTGGGCGGGTAGGGGCCTAACTTCGACAGGTGCGCCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:127857506..127857676 26863196 MeRIP-seq:(Medium) rs1353616979 Functional Loss SNV dbSNP153 33..33 33 - - - 74044 RMVar_ID_74044 Human_SNP_ID_91250060 m1A Human chr2 - 127857563 127857563 127857563 AAAAAGCGGGAAGAGGAGGATTGGTCCGTGTGAACGCAGCTTGGTTTGTTGACTGGCGCACCTGT AAAAAGCGGGAAGAGGAGGATTGGTCCGTGTGGACGCAGCTTGGTTTGTTGACTGGCGCACCTGT T C POLR2D Ensembl:ENSG00000144231 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127857558..127857644 26863196 MeRIP-seq:(Medium) rs1385939974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822529,Human_RBP_ID_13606043,Human_RBP_ID_23283132 74045 RMVar_ID_74045 Human_SNP_ID_91250191 m1A Human chr2 - 127858030 127858030 127858030 AGAGGAGGACGCCTCACAGCTCATCTTTCCTAAAGGTTGGGCTCGGGGCTGCCAGACTCCCCCGC AGAGGAGGACGCCTCACAGCTCATCTTTCCTACAGGTTGGGCTCGGGGCTGCCAGACTCCCCCGC T G POLR2D Ensembl:ENSG00000144231 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:127858024..127858111 26863410 MeRIP-seq:(Medium) rs768484439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4580598,Human_RBP_ID_6822537,Human_RBP_ID_8500625,Human_RBP_ID_9330652,Human_RBP_ID_17939464,Human_RBP_ID_19098201 Human_Splice_Rec_295925,Human_Splice_Rec_295931,Human_Splice_Rec_295935 74046 RMVar_ID_74046 Human_SNP_ID_91250212 m1A Human chr2 + 127858080 127858080 127858080 GAGGCGTCCTCCTCTACGTCGCCAGCCCGCGGATCGCTGCCACCCGCCGCCATCGCCGCGCCGCG GAGGCGTCCTCCTCTACGTCGCCAGCCCGCGGTTCGCTGCCACCCGCCGCCATCGCCGCGCCGCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr2:127857960..127858104;chr2:127857877..127858106 26863196 MeRIP-seq:(Medium) rs1164963630 Functional Loss SNV dbSNP153 33..33 33 - - - 74047 RMVar_ID_74047 Human_SNP_ID_91250216 m1A Human chr2 - 127858085 127858085 127858085 CGCGGCGCGGCGCGGCGATGGCGGCGGGTGGCAGCGATCCGCGGGCTGGCGACGTAGAGGAGGAC CGCGGCGCGGCGCGGCGATGGCGGCGGGTGGCGGCGATCCGCGGGCTGGCGACGTAGAGGAGGAC T C POLR2D Ensembl:ENSG00000144231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:127858001..127858096;chr2:127857896..127858125;chr2:127857902..127858125 26863196 MeRIP-seq:(Medium) rs745343435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4580599,Human_RBP_ID_5500817,Human_RBP_ID_6822538,Human_RBP_ID_9330652 Human_Splice_Rec_295925,Human_Splice_Rec_295931,Human_Splice_Rec_295935 74048 RMVar_ID_74048 Human_SNP_ID_91250217 m1A Human chr2 - 127858085 127858085 127858085 CGCGGCGCGGCGCGGCGATGGCGGCGGGTGGCAGCGATCCGCGGGCTGGCGACGTAGAGGAGGAC CGCGGCGCGGCGCGGCGATGGCGGCGGGTGGCCGCGATCCGCGGGCTGGCGACGTAGAGGAGGAC T G POLR2D Ensembl:ENSG00000144231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:127858001..127858096;chr2:127857896..127858125;chr2:127857902..127858125 26863196 MeRIP-seq:(Medium) rs745343435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4580599,Human_RBP_ID_5500817,Human_RBP_ID_6822538,Human_RBP_ID_9330652 Human_Splice_Rec_295925,Human_Splice_Rec_295931,Human_Splice_Rec_295935 74049 RMVar_ID_74049 Human_SNP_ID_91257515 m1A Human chr2 + 127885981 127885981 127885981 GACGGGGCGGGGCGAAGGAGGCCGGCGGGCGGAGGAGGAAGCGGCGGGGCGGCGGCGGCGGCGGC GACGGGGCGGGGCGAAGGAGGCCGGCGGGCGGTGGAGGAAGCGGCGGGGCGGCGGCGGCGGCGGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:127885910..127886015 26863196 MeRIP-seq:(Medium) rs1406829159 Functional Loss SNV dbSNP153 33..33 33 - - - 74050 RMVar_ID_74050 Human_SNP_ID_91257701 m1A Human chr2 + 127886505 127886505 127886505 TAGTCCGGGACGGGCCCGCAGCATTGTCCGCGACGCAGCTCGGGATCCGCGTCGGGTTGTCGGCC TAGTCCGGGACGGGCCCGCAGCATTGTCCGCGGCGCAGCTCGGGATCCGCGTCGGGTTGTCGGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:127886419..127886581 26863196 MeRIP-seq:(Medium) rs1412360415 Functional Loss SNV dbSNP153 33..33 33 - - - 74051 RMVar_ID_74051 Human_SNP_ID_91282128 m1A Human chr2 + 127981401 127981396 127981401 CCTCACCCCGACCCAGTCCTCCTGCACCCCCGACTCAGCTCCCGCACTCCGACCTAGTCCTCCTG CCTCACCCCGACCCAGTCCTCCTGCACC_____CTCAGCTCCCGCACTCCGACCTAGTCCTCCTG CCCCGA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:127981354..127981651 26863196 MeRIP-seq:(Medium) rs1427384106 Functional Loss DEL dbSNP153 29..33 33 - - - 74052 RMVar_ID_74052 Human_SNP_ID_91282130 m1A Human chr2 + 127981401 127981398 127981401 CCTCACCCCGACCCAGTCCTCCTGCACCCCCGACTCAGCTCCCGCACTCCGACCTAGTCCTCCTG CCTCACCCCGACCCAGTCCTCCTGCACCCC___CTCAGCTCCCGCACTCCGACCTAGTCCTCCTG CCGA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:127981354..127981651 26863196 MeRIP-seq:(Medium) rs1559065125 Functional Loss DEL dbSNP153 31..33 33 - - - 74053 RMVar_ID_74053 Human_SNP_ID_91282157 m1A Human chr2 - 127981451 127981451 127981451 AGTCGGGGGTGCAGGAGGACTAGGTTGGGGTGAGGGAGCTGAGTCGGGTGCAGGAGGACTAGGTC AGTCGGGGGTGCAGGAGGACTAGGTTGGGGTGGGGGAGCTGAGTCGGGTGCAGGAGGACTAGGTC T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127981347..127981627 26863196 MeRIP-seq:(Medium) rs58526435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264398,Human_RBP_ID_8200670,Human_RBP_ID_18442445,Human_RBP_ID_18948229,Human_RBP_ID_23824068 RMVar_hsa_circ_85299,RMVar_hsa_circ_79785,RMVar_hsa_circ_83471,RMVar_hsa_circ_203124,RMVar_hsa_circ_203125,RMVar_hsa_circ_101552,RMVar_hsa_circ_68342,RMVar_hsa_circ_104464,RMVar_hsa_circ_203126,RMVar_hsa_circ_203127,RMVar_hsa_circ_74347,RMVar_hsa_circ_97102,RMVar_hsa_circ_80552,RMVar_hsa_circ_203128,RMVar_hsa_circ_203129,RMVar_hsa_circ_118591,RMVar_hsa_circ_203130,RMVar_hsa_circ_75753,RMVar_hsa_circ_311702,RMVar_hsa_circ_203131,RMVar_hsa_circ_17262,RMVar_hsa_circ_203132,RMVar_hsa_circ_313935,RMVar_hsa_circ_347932,RMVar_hsa_circ_203133,RMVar_hsa_circ_33411 74054 RMVar_ID_74054 Human_SNP_ID_91282158 m1A Human chr2 - 127981451 127981451 127981451 AGTCGGGGGTGCAGGAGGACTAGGTTGGGGTGAGGGAGCTGAGTCGGGTGCAGGAGGACTAGGTC AGTCGGGGGTGCAGGAGGACTAGGTTGGGGTGCGGGAGCTGAGTCGGGTGCAGGAGGACTAGGTC T G SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127981347..127981627 26863196 MeRIP-seq:(Medium) rs58526435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264398,Human_RBP_ID_8200670,Human_RBP_ID_18442445,Human_RBP_ID_18948229,Human_RBP_ID_23824068 RMVar_hsa_circ_85299,RMVar_hsa_circ_79785,RMVar_hsa_circ_83471,RMVar_hsa_circ_203124,RMVar_hsa_circ_203125,RMVar_hsa_circ_101552,RMVar_hsa_circ_68342,RMVar_hsa_circ_104464,RMVar_hsa_circ_203126,RMVar_hsa_circ_203127,RMVar_hsa_circ_74347,RMVar_hsa_circ_97102,RMVar_hsa_circ_80552,RMVar_hsa_circ_203128,RMVar_hsa_circ_203129,RMVar_hsa_circ_118591,RMVar_hsa_circ_203130,RMVar_hsa_circ_75753,RMVar_hsa_circ_311702,RMVar_hsa_circ_203131,RMVar_hsa_circ_17262,RMVar_hsa_circ_203132,RMVar_hsa_circ_313935,RMVar_hsa_circ_347932,RMVar_hsa_circ_203133,RMVar_hsa_circ_33411 74055 RMVar_ID_74055 Human_SNP_ID_91282288 m1A Human chr2 + 127981738 127981738 127981738 CCCAGTCCTCCTGCACCCCCGACAGCTCCCTCACCCCGACGCAGTCCTCCTGCACCCCGACTCAG CCCAGTCCTCCTGCACCCCCGACAGCTCCCTCCCCCCGACGCAGTCCTCCTGCACCCCGACTCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:127981711..127981877 26863196 MeRIP-seq:(Medium) rs998658776 Functional Loss SNV dbSNP153 33..33 33 - - - 74056 RMVar_ID_74056 Human_SNP_ID_91282318 m1A Human chr2 + 127981825 127981825 127981825 TCCTGCACCCTCGACTCAGCTCTCCCACCCCGACCCAGTCCTCTTGCACCCGACTCAGCTCCCCG TCCTGCACCCTCGACTCAGCTCTCCCACCCCGGCCCAGTCCTCTTGCACCCGACTCAGCTCCCCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:127981730..127981903 26863196 MeRIP-seq:(Medium) rs1308532893 Functional Loss SNV dbSNP153 33..33 33 - - - 74057 RMVar_ID_74057 Human_SNP_ID_91289425 m1A Human chr2 - 128009503 128009503 128009503 AGGAGAGATGAAAATGGATGTAGAAAGACATGATTAGATTCTGGGTAGATTATTATTATTTTTTG AGGAGAGATGAAAATGGATGTAGAAAGACATGGTTAGATTCTGGGTAGATTATTATTATTTTTTG T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:128009497..128009613 26863196 MeRIP-seq:(Medium) rs1353978383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13606867 RMVar_hsa_circ_83706,RMVar_hsa_circ_83471,RMVar_hsa_circ_203125,RMVar_hsa_circ_74347,RMVar_hsa_circ_75753,RMVar_hsa_circ_14524,RMVar_hsa_circ_203132,RMVar_hsa_circ_300540,RMVar_hsa_circ_119827,RMVar_hsa_circ_62664,RMVar_hsa_circ_203138,RMVar_hsa_circ_74292,RMVar_hsa_circ_203139,RMVar_hsa_circ_348590,RMVar_hsa_circ_203137,RMVar_hsa_circ_79784,RMVar_hsa_circ_203146,RMVar_hsa_circ_4033,RMVar_hsa_circ_50593,RMVar_hsa_circ_374141,RMVar_hsa_circ_203148 74058 RMVar_ID_74058 Human_SNP_ID_91294211 m1A Human chr2 - 128027125 128027125 128027125 CCTCCGCGGCACCCCCAGGCCGGCGAGATAGAAGCGGGCGGTGCGGGCGGCGGGCGGCGGCTACA CCTCCGCGGCACCCCCAGGCCGGCGAGATAGAGGCGGGCGGTGCGGGCGGCGGGCGGCGGCTACA T C SAP130 Ensembl:ENSG00000136715 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:128027120..128027259 26863196 MeRIP-seq:(Medium) rs1175246498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_295973,Human_Splice_Rec_296011 74059 RMVar_ID_74059 Human_SNP_ID_91294248 m1A Human chr2 + 128027237 128027237 128027237 GCGGCGGCGGCGCCCGGGGCCCGCTGCTGTCCAGCCCCGCTGGCCCCACTCACCCCCGCCACCCG GCGGCGGCGGCGCCCGGGGCCCGCTGCTGTCCGGCCCCGCTGGCCCCACTCACCCCCGCCACCCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:128027051..128027271 26863196 MeRIP-seq:(Medium) rs1023534161 Functional Loss SNV dbSNP153 33..33 33 - - - 74060 RMVar_ID_74060 Human_SNP_ID_91294528 m1A Human chr2 - 128027720 128027720 128027720 TGTCCTGTGGCGAGGAAGGGAGAGGCACCGGGAGGGGTGGGCTGACCCGGGCGTGGGGGCGTGGC TGTCCTGTGGCGAGGAAGGGAGAGGCACCGGGTGGGGTGGGCTGACCCGGGCGTGGGGGCGTGGC T A SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:128027693..128027769 26863196 MeRIP-seq:(Medium) rs575046085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8897,Human_RBP_ID_5195546,Human_RBP_ID_8200678,Human_RBP_ID_8233992 74061 RMVar_ID_74061 Human_SNP_ID_91310796 m1A Human chr2 - 128091404 128091404 128091404 CCTCACGCCACCCCTGGGTACCTGTCACCGGCAGCGCACCCGCGGCACACGCACCGCTCGCGTCT CCTCACGCCACCCCTGGGTACCTGTCACCGGCTGCGCACCCGCGGCACACGCACCGCTCGCGTCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:128091356..128091458 26863196 MeRIP-seq:(Medium) rs1046990722 Functional Loss SNV dbSNP153 33..33 33 - - - 74062 RMVar_ID_74062 Human_SNP_ID_91324213 m1A Human chr2 - 128143147 128143147 128143147 ACTTCTACATACGGATATTTCTTCTCCAGGACACTGACCACATGTTCAACTTTCACTTTTTCTCC ACTTCTACATACGGATATTTCTTCTCCAGGACCCTGACCACATGTTCAACTTTCACTTTTTCTCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:128143027..128143245 26863196 MeRIP-seq:(Medium) rs200271089 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 74063 RMVar_ID_74063 Human_SNP_ID_91336531 m1A Human chr2 + 128192917 128192917 128192917 GAAACAGTTTCCGGTCAGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC GAAACAGTTTCCGGTCAGGCACAGTGGCTTACCCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC A C UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs909245748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1941330,Human_miRNA_ID_1944382,Human_miRNA_ID_2115521,Human_miRNA_ID_2199093,Human_miRNA_ID_2202162,Human_miRNA_ID_2314582,Human_miRNA_ID_2317743,Human_miRNA_ID_2320897,Human_miRNA_ID_2324051,Human_miRNA_ID_2518434,Human_miRNA_ID_2521603,Human_miRNA_ID_2773475,Human_miRNA_ID_2814627,Human_miRNA_ID_2820799,Human_miRNA_ID_2826935,Human_miRNA_ID_2830085,Human_miRNA_ID_2834202,Human_miRNA_ID_2839574,Human_miRNA_ID_2844756,Human_miRNA_ID_2847775,Human_miRNA_ID_2861886,Human_miRNA_ID_3111613 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 74064 RMVar_ID_74064 Human_SNP_ID_91336532 m1A Human chr2 + 128192917 128192917 128192917 GAAACAGTTTCCGGTCAGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC GAAACAGTTTCCGGTCAGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs909245748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1941330,Human_miRNA_ID_1944382,Human_miRNA_ID_2115521,Human_miRNA_ID_2199093,Human_miRNA_ID_2202162,Human_miRNA_ID_2314582,Human_miRNA_ID_2317743,Human_miRNA_ID_2320897,Human_miRNA_ID_2324051,Human_miRNA_ID_2518434,Human_miRNA_ID_2521603,Human_miRNA_ID_2773475,Human_miRNA_ID_2814627,Human_miRNA_ID_2820799,Human_miRNA_ID_2826935,Human_miRNA_ID_2830085,Human_miRNA_ID_2834202,Human_miRNA_ID_2839574,Human_miRNA_ID_2844756,Human_miRNA_ID_2847775,Human_miRNA_ID_2861886,Human_miRNA_ID_3111613 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 74065 RMVar_ID_74065 Human_SNP_ID_91336691 m1A Human chr2 + 128193426 128193426 128193426 GGCGCCTGCCACCATGCCTGGTTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGG GGCGCCTGCCACCATGCCTGGTTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTTACCATGTTGG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1404053660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 74066 RMVar_ID_74066 Human_SNP_ID_91336966 m1A Human chr2 + 128194528 128194528 128194528 ACCTCAAGTGATCCACCCGCATCGGCCCCCCAAAGTGCTGGGATTATAGGCGTGAACCACCGCGC ACCTCAAGTGATCCACCCGCATCGGCCCCCCAGAGTGCTGGGATTATAGGCGTGAACCACCGCGC A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1216547247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 74067 RMVar_ID_74067 Human_SNP_ID_91354734 m1A Human chr2 + 128266328 128266328 128266328 AGCAGATTCCCATTGACCCTGACCTCCCTTTGAAAGAACCACACCACTAAATCCCCTTGGCACTC AGCAGATTCCCATTGACCCTGACCTCCCTTTGCAAGAACCACACCACTAAATCCCCTTGGCACTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:128266217..128266389 26863196 MeRIP-seq:(Medium) rs1292262963 Functional Loss SNV dbSNP153 33..33 33 - - - 74068 RMVar_ID_74068 Human_SNP_ID_91354744 m1A Human chr2 - 128266359 128266359 128266359 TCCCTGGGTGGATGCATCACACTAAGGAAGTGAGTGCCAAGGGGATTTAGTGGTGTGGTTCTTTC TCCCTGGGTGGATGCATCACACTAAGGAAGTGCGTGCCAAGGGGATTTAGTGGTGTGGTTCTTTC T G HS6ST1 Ensembl:ENSG00000136720 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128266226..128266476 32194978 MeRIP-seq:(Medium) rs1459556124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27686553 74069 RMVar_ID_74069 Human_SNP_ID_91354809 m1A Human chr2 - 128266621 128266584 128266621 CTCTCCTGCCCCAGCTTCCACTCAGCCACCACAGTTGCCACACCATGGGGTGGAGACGTGGGTCA CTCTCCTGCCCCAGCTTCCACTCAGCCACCAC_________________________________ CGTGGTGACCCACGTCTCCACCCCATGGTGTGGCAACT C HS6ST1 Ensembl:ENSG00000136720 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128266575..128266725 32194978 MeRIP-seq:(Medium) rs1237805006 Functional Loss DEL dbSNP153 33..65 33 - - - 74070 RMVar_ID_74070 Human_SNP_ID_91354823 m1A Human chr2 - 128266621 128266621 128266621 CTCTCCTGCCCCAGCTTCCACTCAGCCACCACAGTTGCCACACCATGGGGTGGAGACGTGGGTCA CTCTCCTGCCCCAGCTTCCACTCAGCCACCACGGTTGCCACACCATGGGGTGGAGACGTGGGTCA T C HS6ST1 Ensembl:ENSG00000136720 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128266575..128266725 32194978 MeRIP-seq:(Medium) rs981089206 Functional Loss SNV dbSNP153 33..33 33 - - - 74071 RMVar_ID_74071 Human_SNP_ID_91354931 m1A Human chr2 + 128267009 128267009 128267009 GGGAGGGCTGAGTGTCTGTTGTCAGGGAGGCCACCTACAGCTGTTTTGCCAAGGCTAGTTGAGAA GGGAGGGCTGAGTGTCTGTTGTCAGGGAGGCCGCCTACAGCTGTTTTGCCAAGGCTAGTTGAGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:128266999..128267100 26863196 MeRIP-seq:(Medium) rs1477203489 Functional Loss SNV dbSNP153 33..33 33 - - - 74072 RMVar_ID_74072 Human_SNP_ID_91355189 m1A Human chr2 + 128267869 128267869 128267869 TGCGCAAACCTTCAGTTTTTGCGATAAATCCAAGGAGGCCAGGAGAGCAGCTCCAGGCACAACAC TGCGCAAACCTTCAGTTTTTGCGATAAATCCACGGAGGCCAGGAGAGCAGCTCCAGGCACAACAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128267820..128267921 32194978 MeRIP-seq:(Medium) rs1245738549 Functional Loss SNV dbSNP153 33..33 33 - - - 74073 RMVar_ID_74073 Human_SNP_ID_91355346 m1A Human chr2 + 128268238 128268238 128268238 CGCGGCCCGGCTCGTCGGCATCCTCCCGCGGCAGTGCCTCCTTGGCCCGGTGCAGCAGACGCTCC CGCGGCCCGGCTCGTCGGCATCCTCCCGCGGCGGTGCCTCCTTGGCCCGGTGCAGCAGACGCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:128268119..128268244 26863196 MeRIP-seq:(Medium) rs1168168166 Functional Loss SNV dbSNP153 33..33 33 - - - 74074 RMVar_ID_74074 Human_SNP_ID_91355420 m1A Human chr2 + 128268418 128268418 128268418 CGATGCGCCGGATGGTGTCTTCATCCACCTCCACGCCGCCCGCCCGCGTGCTATTGTACTGCATG CGATGCGCCGGATGGTGTCTTCATCCACCTCCGCGCCGCCCGCCCGCGTGCTATTGTACTGCATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128268119..128268419 32194978 MeRIP-seq:(Medium) rs1410891506 Functional Loss SNV dbSNP153 33..33 33 - - - 74075 RMVar_ID_74075 Human_SNP_ID_91359711 m1A Human chr2 - 128284360 128284360 128284360 GGAGGGATGGCAGAGACTTGGGGCCTTGTGTGACTGGGGACAGGTGGCAACAGGTGGGAGGGAGG GGAGGGATGGCAGAGACTTGGGGCCTTGTGTGGCTGGGGACAGGTGGCAACAGGTGGGAGGGAGG T C HS6ST1 Ensembl:ENSG00000136720 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:128284064..128284492 26863196 MeRIP-seq:(Medium) rs1306950584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638850,Human_RBP_ID_5197503,Human_RBP_ID_8200687,Human_RBP_ID_18462598,Human_RBP_ID_22417173,Human_RBP_ID_22699658 74076 RMVar_ID_74076 Human_SNP_ID_91359714 m1A Human chr2 + 128284375 128284375 128284375 TTGCCACCTGTCCCCAGTCACACAAGGCCCCAAGTCTCTGCCATCCCTCCCACATTACACCCATG TTGCCACCTGTCCCCAGTCACACAAGGCCCCAGGTCTCTGCCATCCCTCCCACATTACACCCATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:128284245..128284392 26863196 MeRIP-seq:(Medium) rs890555808 Functional Loss SNV dbSNP153 33..33 33 - - - 74077 RMVar_ID_74077 Human_SNP_ID_91368551 m1A Human chr2 - 128318406 128318406 128318406 GGGCGCGCCCGGCGGCCGCGCGCCGCCCGACGACCTGGACCTGTTCCCCACACCCGACCCCCACT GGGCGCGCCCGGCGGCCGCGCGCCGCCCGACGGCCTGGACCTGTTCCCCACACCCGACCCCCACT T C HS6ST1 Ensembl:ENSG00000136720 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:128318377..128318577 32194978 MeRIP-seq:(Medium) rs1193936218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622687 74078 RMVar_ID_74078 Human_SNP_ID_91834490 m1A Human chr2 - 130160189 130160189 130160189 CGCCAGGGAGGGAGGACAGTGGTCCAGAAAGCATCTGGCAAACCCCATGGTGGGAGGGTGACCAG CGCCAGGGAGGGAGGACAGTGGTCCAGAAAGCCTCTGGCAAACCCCATGGTGGGAGGGTGACCAG T G SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130160138..130160387 26863196 MeRIP-seq:(Medium) rs1558747528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243677,Human_RBP_ID_264399,Human_RBP_ID_3958246,Human_RBP_ID_5196550,Human_RBP_ID_5322183,Human_RBP_ID_5378719,Human_RBP_ID_8234463,Human_RBP_ID_18421892,Human_RBP_ID_22598762,Human_RBP_ID_22669423,Human_RBP_ID_22722032 74079 RMVar_ID_74079 Human_SNP_ID_91836442 m1A Human chr2 + 130167572 130167571 130167572 AGGAGGCTAGTGTGGTGGAGGCCATAGGAAGCAAAGGGTATGGCTGGTGTCCTGAGGGAGACACA AGGAGGCTAGTGTGGTGGAGGCCATAGGAAGC_AAGGGTATGGCTGGTGTCCTGAGGGAGACACA CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130167521..130167626 26863196 MeRIP-seq:(Medium) rs781598476 Functional Loss DEL dbSNP153 33..33 33 - - - 74080 RMVar_ID_74080 Human_SNP_ID_91836444 m1A Human chr2 + 130167572 130167572 130167572 AGGAGGCTAGTGTGGTGGAGGCCATAGGAAGCAAAGGGTATGGCTGGTGTCCTGAGGGAGACACA AGGAGGCTAGTGTGGTGGAGGCCATAGGAAGCCAAGGGTATGGCTGGTGTCCTGAGGGAGACACA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130167521..130167626 26863196 MeRIP-seq:(Medium) rs1314109860 Functional Loss SNV dbSNP153 33..33 33 - - - 74081 RMVar_ID_74081 Human_SNP_ID_91837754 m1A Human chr2 + 130172495 130172495 130172495 CAGTCTGAAGTACGGACGTGGAGGGACACAGGAAGTGGCTGGAAAACCAAGCTAGTTGTTAGCAT CAGTCTGAAGTACGGACGTGGAGGGACACAGGCAGTGGCTGGAAAACCAAGCTAGTTGTTAGCAT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:130172476..130172500 26863196 MeRIP-seq:(Medium) rs569657548 Functional Loss SNV dbSNP153 33..33 33 - - - 74082 RMVar_ID_74082 Human_SNP_ID_91837755 m1A Human chr2 + 130172495 130172495 130172495 CAGTCTGAAGTACGGACGTGGAGGGACACAGGAAGTGGCTGGAAAACCAAGCTAGTTGTTAGCAT CAGTCTGAAGTACGGACGTGGAGGGACACAGGGAGTGGCTGGAAAACCAAGCTAGTTGTTAGCAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:130172476..130172500 26863196 MeRIP-seq:(Medium) rs569657548 Functional Loss SNV dbSNP153 33..33 33 - - - 74083 RMVar_ID_74083 Human_SNP_ID_91840380 m1A Human chr2 - 130181759 130181759 130181759 GCGCCGGAGGCCGCCACAACGCAGGCGCATTCAGCTAAGGACCACTCCCTCCCCCGCACTCCTGC GCGCCGGAGGCCGCCACAACGCAGGCGCATTCGGCTAAGGACCACTCCCTCCCCCGCACTCCTGC T C SMPD4 Ensembl:ENSG00000136699 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130181709..130181823 26863196 MeRIP-seq:(Medium) rs552704948 Functional Loss SNV dbSNP153 33..33 33 - - - 74084 RMVar_ID_74084 Human_SNP_ID_91840680 m1A Human chr2 + 130182352 130182352 130182352 CGGCGCCCCCGGGGCTGGAGGCGGCCCGGCAGAAGCTGGCGCTGCGGCGGAAGAAGGTGCTGAGC CGGCGCCCCCGGGGCTGGAGGCGGCCCGGCAGCAGCTGGCGCTGCGGCGGAAGAAGGTGCTGAGC A C MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:130182251..130182573 26863410 MeRIP-seq:(Medium) rs1046072524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243033,Human_RBP_ID_534080,Human_RBP_ID_776232,Human_RBP_ID_830189,Human_RBP_ID_4581162,Human_RBP_ID_5322190,Human_RBP_ID_8500768,Human_RBP_ID_9331166,Human_RBP_ID_17658166,Human_RBP_ID_17964175 Human_Splice_Rec_297005 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74085 RMVar_ID_74085 Human_SNP_ID_91840691 m1A Human chr2 + 130182373 130182373 130182373 CGGCCCGGCAGAAGCTGGCGCTGCGGCGGAAGAAGGTGCTGAGCACCGAGGAGATGGAGCTGTAC CGGCCCGGCAGAAGCTGGCGCTGCGGCGGAAGTAGGTGCTGAGCACCGAGGAGATGGAGCTGTAC A T MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:130182251..130182475 26863410 MeRIP-seq:(Medium) rs1191293965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243033,Human_RBP_ID_534080,Human_RBP_ID_776233,Human_RBP_ID_1577824,Human_RBP_ID_4581162,Human_RBP_ID_5322190,Human_RBP_ID_9331166,Human_RBP_ID_17658166,Human_RBP_ID_17964175,Human_RBP_ID_23132245,Human_RBP_ID_27000621 Human_Splice_Rec_297005,Human_Splice_Rec_297009,Human_Splice_Rec_297015,Human_Splice_Rec_297019,Human_Splice_Rec_297021 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74086 RMVar_ID_74086 Human_SNP_ID_91840693 m1A Human chr2 - 130182377 130182377 130182377 GCTCGTACAGCTCCATCTCCTCGGTGCTCAGCACCTTCTTCCGCCGCAGCGCCAGCTTCTGCCGG GCTCGTACAGCTCCATCTCCTCGGTGCTCAGCGCCTTCTTCCGCCGCAGCGCCAGCTTCTGCCGG T C SMPD4 Ensembl:ENSG00000136699 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr2:130182251..130182548;chr2:130182226..130182654 26863196 MeRIP-seq:(Medium) rs774668981 Functional Loss SNV dbSNP153 33..33 33 - - - 74087 RMVar_ID_74087 Human_SNP_ID_91840701 m1A Human chr2 - 130182395 130182395 130182395 CGCCCGCCGCCTGCGCCAGCTCGTACAGCTCCATCTCCTCGGTGCTCAGCACCTTCTTCCGCCGC CGCCCGCCGCCTGCGCCAGCTCGTACAGCTCCGTCTCCTCGGTGCTCAGCACCTTCTTCCGCCGC T C SMPD4 Ensembl:ENSG00000136699 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:130182226..130182650 26863196 MeRIP-seq:(Medium) rs759973768 Functional Loss SNV dbSNP153 33..33 33 - - - 74088 RMVar_ID_74088 Human_SNP_ID_91840821 m1A Human chr2 - 130182629 130182629 130182629 GGGCCACGTTCAGCTTCAGCAGGTCCACCAGGATCCTGGCGGGGACAGACGCGGGGCCGGTGAGC GGGCCACGTTCAGCTTCAGCAGGTCCACCAGGGTCCTGGCGGGGACAGACGCGGGGCCGGTGAGC T C SMPD4 Ensembl:ENSG00000136699 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130182626..130182675 26863196 MeRIP-seq:(Medium) rs1280198336 Functional Loss SNV dbSNP153 33..33 33 - - - 74089 RMVar_ID_74089 Human_SNP_ID_91841617 m1A Human chr2 + 130184767 130184767 130184767 CTTGTCACTCCAGGGGATGTTGCTGCTCACTCAGCACTCACTCAGGGCTCTGGGAGCCAGGCCTA CTTGTCACTCCAGGGGATGTTGCTGCTCACTCGGCACTCACTCAGGGCTCTGGGAGCCAGGCCTA A G MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130184765..130184967 26863196 MeRIP-seq:(Medium) rs1278942285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18745919 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74090 RMVar_ID_74090 Human_SNP_ID_91841622 m1A Human chr2 + 130184789 130184789 130184789 CTGCTCACTCAGCACTCACTCAGGGCTCTGGGAGCCAGGCCTAGCTCTCAGGGCAGAGGGTGTGG CTGCTCACTCAGCACTCACTCAGGGCTCTGGGGGCCAGGCCTAGCTCTCAGGGCAGAGGGTGTGG A G MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130184784..130184882 26863196 MeRIP-seq:(Medium) rs1245681176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18745919 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74091 RMVar_ID_74091 Human_SNP_ID_91841842 m1A Human chr2 + 130185481 130185478 130185481 CAGCCTGGGCAACAGAGCAAGACCCTGTCTCAAAAAAAAAAAAAAAAGAAAAACCGCTAGCAATG CAGCCTGGGCAACAGAGCAAGACCCTGTCT___AAAAAAAAAAAAAAGAAAAACCGCTAGCAATG TCAA T MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:130185479..130185709 26863196 MeRIP-seq:(Medium) rs1365004177 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74092 RMVar_ID_74092 Human_SNP_ID_91843284 m1A Human chr2 + 130190408 130190408 130190408 AGACACAAATGTTGCCCAAGGACCACGAGTACAGCAGGTGCTGCAGTTACGGGGCACGCCCATTC AGACACAAATGTTGCCCAAGGACCACGAGTACGGCAGGTGCTGCAGTTACGGGGCACGCCCATTC A G MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:130190404..130190675 26863410 MeRIP-seq:(Medium) rs1314761385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22547584 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 74093 RMVar_ID_74093 Human_SNP_ID_91843301 m1A Human chr2 - 130190454 130190454 130190454 CGCTGCCTTTGTTTCTCCCTGAGGAGACACAAAGCACAATGATTAGGAATGGGCGTGCCCCGTAA CGCTGCCTTTGTTTCTCCCTGAGGAGACACAAGGCACAATGATTAGGAATGGGCGTGCCCCGTAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130190451..130190700 32194978 MeRIP-seq:(Medium) rs746303481 Functional Loss SNV dbSNP153 33..33 33 - - - 74094 RMVar_ID_74094 Human_SNP_ID_91848842 m1A Human chr2 - 130211231 130211231 130211231 TTTATACTTGAAAATGACAGCCTTAAATGCTCATATCAGTCACAAATCTAGGATGTACTGTCTTG TTTATACTTGAAAATGACAGCCTTAAATGCTCGTATCAGTCACAAATCTAGGATGTACTGTCTTG T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs982318699 Functional Loss SNV dbSNP153 33..33 33 - - - 74095 RMVar_ID_74095 Human_SNP_ID_91854124 m1A Human chr2 + 130230790 130230790 130230790 CTGCTCTCGGGGAGCTCGGGGGCCTTCATCCCAGTGCTGCCTTTCATCCTGGAGATGTTCCAGCA CTGCTCTCGGGGAGCTCGGGGGCCTTCATCCCGGTGCTGCCTTTCATCCTGGAGATGTTCCAGCA A G NOC2LP1 Ensembl:ENSG00000213225 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1302849085 Functional Loss SNV dbSNP153 33..33 33 - - - 74096 RMVar_ID_74096 Human_SNP_ID_91879608 m1A Human chr2 - 130337143 130337143 130337143 TTCCTGGTTTTCACCCAGGTGGCCCGGGTTCGACTCCCGGTATGGGAACAAAAGTGGCTTTTTTT TTCCTGGTTTTCACCCAGGTGGCCCGGGTTCGGCTCCCGGTATGGGAACAAAAGTGGCTTTTTTT T C tRNA-Glu-TTC-1-2 RNACentral:URS0000639DBE tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs959003940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534102,Human_RBP_ID_1192964,Human_RBP_ID_1577831,Human_RBP_ID_1897631,Human_RBP_ID_3594972,Human_RBP_ID_4627090,Human_RBP_ID_5275477,Human_RBP_ID_5469883,Human_RBP_ID_5594652,Human_RBP_ID_6823341,Human_RBP_ID_8500781,Human_RBP_ID_9093599,Human_RBP_ID_9939238,Human_RBP_ID_17085796,Human_RBP_ID_17966451,Human_RBP_ID_18442464,Human_RBP_ID_18745930,Human_RBP_ID_20458609,Human_RBP_ID_22816610,Human_RBP_ID_23110539,Human_RBP_ID_23132247,Human_RBP_ID_23824432,Human_RBP_ID_24420494,Human_RBP_ID_24490652,Human_RBP_ID_25579188,Human_RBP_ID_27017165,Human_RBP_ID_27158152,Human_RBP_ID_27686562 74097 RMVar_ID_74097 Human_SNP_ID_91880322 m1A Human chr2 + 130339641 130339641 130339641 CTCTAGATGGCTTTTGCTGATGTCTCTGCTGGAACAGCTGCTGCCCAGTCCTCCGGGCAGCTCTC CTCTAGATGGCTTTTGCTGATGTCTCTGCTGGGACAGCTGCTGCCCAGTCCTCCGGGCAGCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130339639..130339852 26863196 MeRIP-seq:(Medium) rs752548717 Functional Loss SNV dbSNP153 33..33 33 - - - 74098 RMVar_ID_74098 Human_SNP_ID_91880995 m1A Human chr2 - 130341946 130341946 130341946 TAAACTGAGTCTCACCGCTTTCCTCTCCCTGCAGGGCTGGCTCTCGCTCGCCAAGGCTCGCTACG TAAACTGAGTCTCACCGCTTTCCTCTCCCTGCGGGGCTGGCTCTCGCTCGCCAAGGCTCGCTACG T C CCDC115 Ensembl:ENSG00000136710 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr2:130341899..130342135;chr2:130341932..130342048 26863196,32194978 MeRIP-seq:(Medium) rs765309029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5378723 74099 RMVar_ID_74099 Human_SNP_ID_91881068 m1A Human chr2 + 130342114 130342114 130342114 AGGACCAGCGAATCCAGCTCCGCTCGCAGGTCAAGCGCCGCCATGGACACACCTCCAGATCTGGA AGGACCAGCGAATCCAGCTCCGCTCGCAGGTCGAGCGCCGCCATGGACACACCTCCAGATCTGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:130341939..130342138 26863196 MeRIP-seq:(Medium) rs1197719969 Functional Loss SNV dbSNP153 33..33 33 - - - 74100 RMVar_ID_74100 Human_SNP_ID_91881418 m1A Human chr2 + 130342926 130342926 130342926 CACAGATTCTCCCGGACCCACGTGGAAGCGGCACTCAAGATGGTAGGAGAATGAGCTCCTGTTTC CACAGATTCTCCCGGACCCACGTGGAAGCGGCCCTCAAGATGGTAGGAGAATGAGCTCCTGTTTC A C IMP4 Ensembl:ENSG00000136718 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:130342876..130343223;chr2:130342876..130343066;chr2:130342876..130343005 26863196 MeRIP-seq:(Medium) rs1465172532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623621,Human_RBP_ID_22997454 Human_Splice_Rec_297075,Human_Splice_Rec_297091,Human_Splice_Rec_297101,Human_Splice_Rec_297127,Human_Splice_Rec_297141,Human_Splice_Rec_297149,Human_Splice_Rec_297165,Human_Splice_Rec_297181,Human_Splice_Rec_297189,Human_Splice_Rec_297207 Human_miRNA_ID_2515665,Human_miRNA_ID_2864742 RMVar_hsa_circ_76259,RMVar_hsa_circ_203241 74101 RMVar_ID_74101 Human_SNP_ID_91881424 m1A Human chr2 - 130342937 130342937 130342937 CCCGGACCTCCGAAACAGGAGCTCATTCTCCTACCATCTTGAGTGCCGCTTCCACGTGGGTCCGG CCCGGACCTCCGAAACAGGAGCTCATTCTCCTGCCATCTTGAGTGCCGCTTCCACGTGGGTCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130342876..130342989 26863196 MeRIP-seq:(Medium) rs745410531 Functional Loss SNV dbSNP153 33..33 33 - - - 74102 RMVar_ID_74102 Human_SNP_ID_91881531 m1A Human chr2 + 130343128 130343128 130343128 AGGCCCGCCTGCGCCGCGAGTACCTGTACCGCAAGGCCCGGGAGGAGGCGCAGCGCTCAGCCCAG AGGCCCGCCTGCGCCGCGAGTACCTGTACCGCTAGGCCCGGGAGGAGGCGCAGCGCTCAGCCCAG A T IMP4 Ensembl:ENSG00000136718 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130343115..130343290 32194978 MeRIP-seq:(Medium) rs779644628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775773,Human_RBP_ID_830300,Human_RBP_ID_4623622,Human_RBP_ID_9384737 Human_Splice_Rec_297076,Human_Splice_Rec_297077,Human_Splice_Rec_297092,Human_Splice_Rec_297093,Human_Splice_Rec_297102,Human_Splice_Rec_297103,Human_Splice_Rec_297115,Human_Splice_Rec_297128,Human_Splice_Rec_297129,Human_Splice_Rec_297139,Human_Splice_Rec_297142,Human_Splice_Rec_297143,Human_Splice_Rec_297150,Human_Splice_Rec_297151,Human_Splice_Rec_297166,Human_Splice_Rec_297167,Human_Splice_Rec_297182,Human_Splice_Rec_297183,Human_Splice_Rec_297190,Human_Splice_Rec_297191,Human_Splice_Rec_297193,Human_Splice_Rec_297208,Human_Splice_Rec_297209 RMVar_hsa_circ_76259,RMVar_hsa_circ_100855,RMVar_hsa_circ_203241,RMVar_hsa_circ_203242 74103 RMVar_ID_74103 Human_SNP_ID_91881560 m1A Human chr2 + 130343193 130343193 130343193 GAGAGGAAGGAGCGGCTGCGGCGCGCGCTGGAAGGTAAGGCATCGGCCCCGCGGGCGTCTGCGTG GAGAGGAAGGAGCGGCTGCGGCGCGCGCTGGAGGGTAAGGCATCGGCCCCGCGGGCGTCTGCGTG A G IMP4 Ensembl:ENSG00000136718 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130343151..130343200 26863196 MeRIP-seq:(Medium) rs1043085989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5118583,Human_RBP_ID_9384737,Human_RBP_ID_19098232 Human_Splice_Rec_297077,Human_Splice_Rec_297093,Human_Splice_Rec_297103,Human_Splice_Rec_297115,Human_Splice_Rec_297129,Human_Splice_Rec_297139,Human_Splice_Rec_297143,Human_Splice_Rec_297151,Human_Splice_Rec_297167,Human_Splice_Rec_297183,Human_Splice_Rec_297191,Human_Splice_Rec_297193,Human_Splice_Rec_297209 RMVar_hsa_circ_76259,RMVar_hsa_circ_100855,RMVar_hsa_circ_203241,RMVar_hsa_circ_203242 74104 RMVar_ID_74104 Human_SNP_ID_91881561 m1A Human chr2 + 130343193 130343193 130343193 GAGAGGAAGGAGCGGCTGCGGCGCGCGCTGGAAGGTAAGGCATCGGCCCCGCGGGCGTCTGCGTG GAGAGGAAGGAGCGGCTGCGGCGCGCGCTGGATGGTAAGGCATCGGCCCCGCGGGCGTCTGCGTG A T IMP4 Ensembl:ENSG00000136718 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130343151..130343200 26863196 MeRIP-seq:(Medium) rs1043085989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5118583,Human_RBP_ID_9384737,Human_RBP_ID_19098232 Human_Splice_Rec_297077,Human_Splice_Rec_297093,Human_Splice_Rec_297103,Human_Splice_Rec_297115,Human_Splice_Rec_297129,Human_Splice_Rec_297139,Human_Splice_Rec_297143,Human_Splice_Rec_297151,Human_Splice_Rec_297167,Human_Splice_Rec_297183,Human_Splice_Rec_297191,Human_Splice_Rec_297193,Human_Splice_Rec_297209 RMVar_hsa_circ_76259,RMVar_hsa_circ_100855,RMVar_hsa_circ_203241,RMVar_hsa_circ_203242 74105 RMVar_ID_74105 Human_SNP_ID_91881986 m1A Human chr2 - 130344583 130344583 130344583 AGAGAGGGGCTGAGTGAGTCACAAGCATGGAGACCTCAGCTCATCCAATACACCACAGCTTATTA AGAGAGGGGCTGAGTGAGTCACAAGCATGGAGGCCTCAGCTCATCCAATACACCACAGCTTATTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130344581..130344702 26863196 MeRIP-seq:(Medium) rs1180147803 Functional Loss SNV dbSNP153 33..33 33 - - - 74106 RMVar_ID_74106 Human_SNP_ID_91882292 m1A Human chr2 + 130345483 130345483 130345483 GAGACCCCAGTTCCCGCCTCAAGATGTTTGCAAAGGTACTGGTGAGCAGGGAGTGAGGGAGAGAC GAGACCCCAGTTCCCGCCTCAAGATGTTTGCAGAGGTACTGGTGAGCAGGGAGTGAGGGAGAGAC A G IMP4 Ensembl:ENSG00000136718 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130345401..130345500 32194978 MeRIP-seq:(Medium) rs771333403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9384740,Human_RBP_ID_19101656 Human_Splice_Rec_297081,Human_Splice_Rec_297119,Human_Splice_Rec_297133,Human_Splice_Rec_297147,Human_Splice_Rec_297155,Human_Splice_Rec_297171,Human_Splice_Rec_297187,Human_Splice_Rec_297197,Human_Splice_Rec_297213,Human_Splice_Rec_297227 Human_miRNA_ID_1310875,Human_miRNA_ID_2644310 RMVar_hsa_circ_97073,RMVar_hsa_circ_76259,RMVar_hsa_circ_100855,RMVar_hsa_circ_203241,RMVar_hsa_circ_203242,RMVar_hsa_circ_120858,RMVar_hsa_circ_203243,RMVar_hsa_circ_203244 74107 RMVar_ID_74107 Human_SNP_ID_91882375 m1A Human chr2 - 130345667 130345665 130345668 CAGGTGTGCCCCGATGCTCGTGAACGACCAGCAGATCGGTGACGCCGTTGGCTTTGCAGGCTCGC CAGGTGTGCCCCGATGCTCGTGAACGACCAG___ATCGGTGACGCCGTTGGCTTTGCAGGCTCGC TCTG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130345618..130345718 32194978 MeRIP-seq:(Medium) rs765588715 Functional Loss DEL dbSNP153 32..34 33 - - - 74108 RMVar_ID_74108 Human_SNP_ID_91882376 m1A Human chr2 - 130345667 130345667 130345667 CAGGTGTGCCCCGATGCTCGTGAACGACCAGCAGATCGGTGACGCCGTTGGCTTTGCAGGCTCGC CAGGTGTGCCCCGATGCTCGTGAACGACCAGCGGATCGGTGACGCCGTTGGCTTTGCAGGCTCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130345618..130345718 32194978 MeRIP-seq:(Medium) rs1446052044 Functional Loss SNV dbSNP153 33..33 33 - - - 74109 RMVar_ID_74109 Human_SNP_ID_91882387 m1A Human chr2 + 130345693 130345693 130345693 CCGATCTGCTGGTCGTTCACGAGCATCGGGGCACACCTGGTAAGGCCGGAGGGAGGGAGTCGGGG CCGATCTGCTGGTCGTTCACGAGCATCGGGGCGCACCTGGTAAGGCCGGAGGGAGGGAGTCGGGG A G IMP4 Ensembl:ENSG00000136718 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr2:130345363..130345875;chr2:130345642..130345793;chr2:130345568..130345767 26863196,32194978 MeRIP-seq:(Medium) rs201808299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830302 Human_Splice_Rec_297083,Human_Splice_Rec_297097,Human_Splice_Rec_297107,Human_Splice_Rec_297121,Human_Splice_Rec_297157,Human_Splice_Rec_297173,Human_Splice_Rec_297199,Human_Splice_Rec_297215,Human_Splice_Rec_297229,Human_Splice_Rec_297237,Human_Splice_Rec_297243 RMVar_hsa_circ_97073,RMVar_hsa_circ_76259,RMVar_hsa_circ_100855,RMVar_hsa_circ_203241,RMVar_hsa_circ_203242,RMVar_hsa_circ_32526,RMVar_hsa_circ_120858,RMVar_hsa_circ_203243,RMVar_hsa_circ_125211,RMVar_hsa_circ_203244,RMVar_hsa_circ_203245 74110 RMVar_ID_74110 Human_SNP_ID_91882720 m1A Human chr2 - 130346415 130346415 130346415 TCTCTTGCGTGCGGTATTGGTGTAAGGGTGCCAGCGCCACTCCACGTCTGCTGTGGCCTCCTGCT TCTCTTGCGTGCGGTATTGGTGTAAGGGTGCCGGCGCCACTCCACGTCTGCTGTGGCCTCCTGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130346360..130346455 26863196 MeRIP-seq:(Medium) rs1371518563 Functional Loss SNV dbSNP153 33..33 33 - - - 74111 RMVar_ID_74111 Human_SNP_ID_91883041 m1A Human chr2 - 130347513 130347512 130347513 GAATTTTTGGGGGACACAAACATTCAGGCCACAGCAGTATCCAAACTATATAAGGGACTCAAGTC GAATTTTTGGGGGACACAAACATTCAGGCCAC_GCAGTATCCAAACTATATAAGGGACTCAAGTC CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:130347463..130347662 32194978 MeRIP-seq:(Medium) rs1317217465 Functional Loss DEL dbSNP153 33..33 33 - - - 74112 RMVar_ID_74112 Human_SNP_ID_91889202 m1A Human chr2 - 130370177 130370177 130370177 TGAAGCCCATTTCCAAAACCTGCAGTGGACACAGAGGGGTTCAGGGCCAGATCCCTGGAGGCGAC TGAAGCCCATTTCCAAAACCTGCAGTGGACACGGAGGGGTTCAGGGCCAGATCCCTGGAGGCGAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:130369806..130370177 32194978 MeRIP-seq:(Medium) rs772480824 Functional Loss SNV dbSNP153 33..33 33 - - - 74113 RMVar_ID_74113 Human_SNP_ID_91890119 m1A Human chr2 - 130372901 130372901 130372901 TGAGCTCCACCCGCCACGTCCTCGTAGGCGCCAGATCCGGCAGGACTTTGGTCAGCAGGAACTGA TGAGCTCCACCCGCCACGTCCTCGTAGGCGCCGGATCCGGCAGGACTTTGGTCAGCAGGAACTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130372860..130373169 26863196 MeRIP-seq:(Medium) rs1204388503 Functional Loss SNV dbSNP153 33..33 33 - - - 74114 RMVar_ID_74114 Human_SNP_ID_91890363 m1A Human chr2 + 130373818 130373818 130373818 AGCCAGAGAGAGAGAGACCAGCCAACAGCTTGATAGACCAGTGCAGCCAGAGAGACCACCAAACA AGCCAGAGAGAGAGAGACCAGCCAACAGCTTGTTAGACCAGTGCAGCCAGAGAGACCACCAAACA A T PTPN18 Ensembl:ENSG00000072135 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:130373600..130373962;chr2:130373616..130373966 26863196 MeRIP-seq:(Medium) rs1271130557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534168,Human_RBP_ID_4581334 RMVar_hsa_circ_127523,RMVar_hsa_circ_203249 74115 RMVar_ID_74115 Human_SNP_ID_91890364 m1A Human chr2 - 130373819 130373819 130373819 CTGTTTGGTGGTCTCTCTGGCTGCACTGGTCTATCAAGCTGTTGGCTGGTCTCTCTCTCTCTGGC CTGTTTGGTGGTCTCTCTGGCTGCACTGGTCTGTCAAGCTGTTGGCTGGTCTCTCTCTCTCTGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130373666..130373933 26863196 MeRIP-seq:(Medium) rs945602930 Functional Loss SNV dbSNP153 33..33 33 - - - 74116 RMVar_ID_74116 Human_SNP_ID_92003602 m1A Human chr2 + 130836954 130836954 130836954 GCGGCCGGGCTCCGGGCGTCCCGGCGGCCACCATGCTCAGCGTCGTGCACTTCCTCCGGAGCTTC GCGGCCGGGCTCCGGGCGTCCCGGCGGCCACCGTGCTCAGCGTCGTGCACTTCCTCCGGAGCTTC A G ARHGEF4 Ensembl:ENSG00000136002 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130836906..130837056 26863196 MeRIP-seq:(Medium) rs1044070880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_297725 74117 RMVar_ID_74117 Human_SNP_ID_92006617 m1A Human chr2 + 130847935 130847935 130847935 GAGGCTAGGTCTGAGCCTCAGGAGTGTGTGGGATTGGAGCTGGGCCGCTGGGCTGGGGTCTGTCT GAGGCTAGGTCTGAGCCTCAGGAGTGTGTGGGTTTGGAGCTGGGCCGCTGGGCTGGGGTCTGTCT A T ARHGEF4 Ensembl:ENSG00000136002 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130847920..130848141 26863196 MeRIP-seq:(Medium) rs1278199393 Functional Loss SNV dbSNP153 33..33 33 - - - 74118 RMVar_ID_74118 Human_SNP_ID_92022450 m1A Human chr2 - 130915776 130915776 130915776 CCTGCTTTGGGCTCCAGCTGCCGGCCCCCGGCACCCCCAGGCCCCTGTTCACCCTCCTCAGCCCC CCTGCTTTGGGCTCCAGCTGCCGGCCCCCGGCTCCCCCAGGCCCCTGTTCACCCTCCTCAGCCCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:130915732..130915830 26863196 MeRIP-seq:(Medium) rs1178134012 Functional Loss SNV dbSNP153 33..33 33 - - - 74119 RMVar_ID_74119 Human_SNP_ID_92022451 m1A Human chr2 - 130915776 130915776 130915776 CCTGCTTTGGGCTCCAGCTGCCGGCCCCCGGCACCCCCAGGCCCCTGTTCACCCTCCTCAGCCCC CCTGCTTTGGGCTCCAGCTGCCGGCCCCCGGCGCCCCCAGGCCCCTGTTCACCCTCCTCAGCCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:130915732..130915830 26863196 MeRIP-seq:(Medium) rs1178134012 Functional Loss SNV dbSNP153 33..33 33 - - - 74120 RMVar_ID_74120 Human_SNP_ID_92022690 m1A Human chr2 - 130916220 130916220 130916220 ACGCGGGGGCGCTGGCCCCGGGCTGCTGCAGCACCGCCTTCGGGGGCCTCCTCCGGGCCACGCTC ACGCGGGGGCGCTGGCCCCGGGCTGCTGCAGCCCCGCCTTCGGGGGCCTCCTCCGGGCCACGCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:130916170..130916257 26863196 MeRIP-seq:(Medium) rs1327722157 Functional Loss SNV dbSNP153 33..33 33 - - - 74121 RMVar_ID_74121 Human_SNP_ID_92037364 m1A Human chr2 - 130976908 130976883 130976909 CACACCACACATACTAACACACCATACACACCACACACTAATGCATACCACACACACACCATGCT CACACCACACATACTAACACACCATACACAC__________________________ACCATGCT TGTGTGTGTGGTATGCATTAGTGTGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:130976858..130977316 26863196 MeRIP-seq:(Medium) rs1294026997 Functional Loss DEL dbSNP153 32..57 33 - - - 74122 RMVar_ID_74122 Human_SNP_ID_92056832 m1A Human chr2 - 131051816 131051816 131051816 GGAAGCCACAGCTGCTTGGGTGCAGCTGGTTCATGGACATCCCTTTGAGTTTAGGCTTGGTGGAG GGAAGCCACAGCTGCTTGGGTGCAGCTGGTTCTTGGACATCCCTTTGAGTTTAGGCTTGGTGGAG T A FAM168B Ensembl:ENSG00000152102 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131051766..131051840 26863196 MeRIP-seq:(Medium) rs1307307381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534293,Human_RBP_ID_1020136,Human_RBP_ID_4581512,Human_RBP_ID_6823668,Human_RBP_ID_8201679,Human_RBP_ID_8500863,Human_RBP_ID_8842204,Human_RBP_ID_9093660,Human_RBP_ID_13609542,Human_RBP_ID_17388802,Human_RBP_ID_17699949,Human_RBP_ID_17939751,Human_RBP_ID_18309878,Human_RBP_ID_18745971,Human_RBP_ID_23824733,Human_RBP_ID_27000680,Human_RBP_ID_27686645 Human_miRNA_ID_1747781,Human_miRNA_ID_3096991 RMVar_hsa_circ_203262,RMVar_hsa_circ_81988,RMVar_hsa_circ_100798,RMVar_hsa_circ_103893,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,RMVar_hsa_circ_203261 74123 RMVar_ID_74123 Human_SNP_ID_92057909 m1A Human chr2 + 131055604 131055604 131055604 TGGGGGTAGGCACTTCGCACAGGGTACACGGCAGTCTGGTAGGGGTTCGGGGAGGAGGAGTACGG TGGGGGTAGGCACTTCGCACAGGGTACACGGCCGTCTGGTAGGGGTTCGGGGAGGAGGAGTACGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131055532..131055644 26863196 MeRIP-seq:(Medium) rs749412899 Functional Loss SNV dbSNP153 33..33 33 - - - 74124 RMVar_ID_74124 Human_SNP_ID_92057910 m1A Human chr2 + 131055604 131055604 131055604 TGGGGGTAGGCACTTCGCACAGGGTACACGGCAGTCTGGTAGGGGTTCGGGGAGGAGGAGTACGG TGGGGGTAGGCACTTCGCACAGGGTACACGGCGGTCTGGTAGGGGTTCGGGGAGGAGGAGTACGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131055532..131055644 26863196 MeRIP-seq:(Medium) rs749412899 Functional Loss SNV dbSNP153 33..33 33 - - - 74125 RMVar_ID_74125 Human_SNP_ID_92065508 m1A Human chr2 - 131082646 131082646 131082646 ATTCCCTTTTTTTTCTTTTAGTTTTTGAAATCATGAATCCTGTTTATAGTCCTGGATCTTCTGGG ATTCCCTTTTTTTTCTTTTAGTTTTTGAAATCGTGAATCCTGTTTATAGTCCTGGATCTTCTGGG T C FAM168B Ensembl:ENSG00000152102 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:131082576..131082705;chr2:131082576..131082675 26863196 MeRIP-seq:(Medium) rs749663774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59634,Human_RBP_ID_1577922,Human_RBP_ID_1897730,Human_RBP_ID_3595105,Human_RBP_ID_4581560,Human_RBP_ID_13610604,Human_RBP_ID_25461893 Human_Splice_Rec_297952,Human_Splice_Rec_297953,Human_Splice_Rec_297964,Human_Splice_Rec_297965 Human_miRNA_ID_2616929 RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203268,RMVar_hsa_circ_352585,RMVar_hsa_circ_315146,RMVar_hsa_circ_87954,RMVar_hsa_circ_203269,RMVar_hsa_circ_203271,RMVar_hsa_circ_203270,RMVar_hsa_circ_277089,RMVar_hsa_circ_346190,RMVar_hsa_circ_117352,RMVar_hsa_circ_203272,RMVar_hsa_circ_303327,RMVar_hsa_circ_203273 74126 RMVar_ID_74126 Human_SNP_ID_92068925 m1A Human chr2 - 131092868 131092868 131092868 GGGGGCAGAGCTTTGTGACAATAGTCATTTCCAATGTGTAACTGCTCACTTTGTCTACCCACGAA GGGGGCAGAGCTTTGTGACAATAGTCATTTCCGATGTGTAACTGCTCACTTTGTCTACCCACGAA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:131092864..131092976 32194978 MeRIP-seq:(Medium) rs979710815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1577930,Human_RBP_ID_1897745,Human_RBP_ID_8500901,Human_RBP_ID_13610995 RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 74127 RMVar_ID_74127 Human_SNP_ID_92069160 m1A Human chr2 - 131093393 131093393 131093393 GAGCGCGGGCTGCGGAGAGGCGGGCCGGGCCAAGCGGAGCCGAGCGAGCGGGAGCGCGGCGTCCG GAGCGCGGGCTGCGGAGAGGCGGGCCGGGCCATGCGGAGCCGAGCGAGCGGGAGCGCGGCGTCCG T A FAM168B Ensembl:ENSG00000152102 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:131093237..131093460;chr2:131093201..131093427 26863196 MeRIP-seq:(Medium) rs1468329630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243043,Human_RBP_ID_776246,Human_RBP_ID_828734,Human_RBP_ID_4581572,Human_RBP_ID_5239875,Human_RBP_ID_9330664,Human_RBP_ID_17139001 Human_Splice_Rec_297951 RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 74128 RMVar_ID_74128 Human_SNP_ID_92069175 m1A Human chr2 + 131093415 131093415 131093415 TCGGCTCCGCTTGGCCCGGCCCGCCTCTCCGCAGCCCGCGCTCCCCGCCGACGCTGCGCAGCCAC TCGGCTCCGCTTGGCCCGGCCCGCCTCTCCGCGGCCCGCGCTCCCCGCCGACGCTGCGCAGCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131082654..131093475 26863196 MeRIP-seq:(Medium) rs950808022 Functional Loss SNV dbSNP153 33..33 33 - - - 74129 RMVar_ID_74129 Human_SNP_ID_92072742 m1A Human chr2 - 131105393 131105393 131105393 TCGTCCGGACTAAACAGGGACACTCACCTGCGAACCAGCGTGGAGAACACCAAGACGCCACGGCG TCGTCCGGACTAAACAGGGACACTCACCTGCGTACCAGCGTGGAGAACACCAAGACGCCACGGCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:131105344..131107507 26863196 MeRIP-seq:(Medium) rs1288931794 Functional Loss SNV dbSNP153 33..33 33 - - - 74130 RMVar_ID_74130 Human_SNP_ID_92072746 m1A Human chr2 + 131105397 131105397 131105397 GTGGCGTCTTGGTGTTCTCCACGCTGGTTCGCAGGTGAGTGTCCCTGTTTAGTCCGGACGACCCT GTGGCGTCTTGGTGTTCTCCACGCTGGTTCGCGGGTGAGTGTCCCTGTTTAGTCCGGACGACCCT A G PLEKHB2 Ensembl:ENSG00000115762 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:131105351..131105448;chr2:131105363..131105447;chr2:131105351..131105464 26863196 MeRIP-seq:(Medium) rs1327077648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1020153,Human_RBP_ID_4623633,Human_RBP_ID_9387431,Human_RBP_ID_19101675,Human_RBP_ID_22669435,Human_RBP_ID_23824881 Human_Splice_Rec_297975,Human_Splice_Rec_297989,Human_Splice_Rec_298005,Human_Splice_Rec_298015,Human_Splice_Rec_298029,Human_Splice_Rec_298039,Human_Splice_Rec_298041,Human_Splice_Rec_298047,Human_Splice_Rec_298059 RMVar_hsa_circ_107100,RMVar_hsa_circ_203274 74131 RMVar_ID_74131 Human_SNP_ID_92077938 m1A Human chr2 + 131125715 131125715 131125715 TCCAACTTGGGCGAAATAGTAAGACTGTCTCTAAAAAAAAAAAAACAACCGTACTATTTTTTTTT TCCAACTTGGGCGAAATAGTAAGACTGTCTCTCAAAAAAAAAAAACAACCGTACTATTTTTTTTT A C PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:131125711..131125838 26863196 MeRIP-seq:(Medium) rs556178539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13672,RMVar_hsa_circ_107100,RMVar_hsa_circ_376122,RMVar_hsa_circ_203274,RMVar_hsa_circ_370747,RMVar_hsa_circ_203275,RMVar_hsa_circ_203276 74132 RMVar_ID_74132 Human_SNP_ID_92077939 m1A Human chr2 + 131125715 131125715 131125715 TCCAACTTGGGCGAAATAGTAAGACTGTCTCTAAAAAAAAAAAAACAACCGTACTATTTTTTTTT TCCAACTTGGGCGAAATAGTAAGACTGTCTCTGAAAAAAAAAAAACAACCGTACTATTTTTTTTT A G PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:131125711..131125838 26863196 MeRIP-seq:(Medium) rs556178539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13672,RMVar_hsa_circ_107100,RMVar_hsa_circ_376122,RMVar_hsa_circ_203274,RMVar_hsa_circ_370747,RMVar_hsa_circ_203275,RMVar_hsa_circ_203276 74133 RMVar_ID_74133 Human_SNP_ID_92078228 m1A Human chr2 - 131126732 131126728 131126732 CACAAAGACTAATTGTTTTCCCATCTCGACAAACAATCTGGAGCATGCAGTCTTTTGACTTTCCA CACAAAGACTAATTGTTTTCCCATCTCGACAA____TCTGGAGCATGCAGTCTTTTGACTTTCCA ATTGT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:131125757..131126736 32194978 MeRIP-seq:(Medium) rs1409367432 Functional Loss DEL dbSNP153 33..36 33 - - - 74134 RMVar_ID_74134 Human_SNP_ID_92083816 m1A Human chr2 - 131149150 131149150 131149150 ACCCAGTATGCATTTCATACCAGGATCAAGTCACTAATGACAGCCAAGTTCCAGGCTTATCTATG ACCCAGTATGCATTTCATACCAGGATCAAGTCGCTAATGACAGCCAAGTTCCAGGCTTATCTATG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:131149126..131149150 32194978 MeRIP-seq:(Medium) rs781539034 Functional Loss SNV dbSNP153 33..33 33 - - - 74135 RMVar_ID_74135 Human_SNP_ID_92083817 m1A Human chr2 - 131149150 131149150 131149150 ACCCAGTATGCATTTCATACCAGGATCAAGTCACTAATGACAGCCAAGTTCCAGGCTTATCTATG ACCCAGTATGCATTTCATACCAGGATCAAGTCCCTAATGACAGCCAAGTTCCAGGCTTATCTATG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:131149126..131149150 32194978 MeRIP-seq:(Medium) rs781539034 Functional Loss SNV dbSNP153 33..33 33 - - - 74136 RMVar_ID_74136 Human_SNP_ID_92083865 m1A Human chr2 + 131149345 131149345 131149345 GTTACAAGAAACTTCTTATTCAGGTTTGAGTAAGCATTTTACTTCCATGTGTACTTTTAAATAAT GTTACAAGAAACTTCTTATTCAGGTTTGAGTAGGCATTTTACTTCCATGTGTACTTTTAAATAAT A G PLEKHB2 Ensembl:ENSG00000115762 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:131149245..131149346 32194978 MeRIP-seq:(Medium) rs909180471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1897767,Human_RBP_ID_17939809,Human_RBP_ID_27686713 74137 RMVar_ID_74137 Human_SNP_ID_92127726 m1A Human chr2 + 131299492 131299492 131299492 GAAGGGCAGCGGGAAGGAGGCGTGCGGGCCGTAGGGGCTGAGGGGCAGGTGTTGGGGGCGGAATG GAAGGGCAGCGGGAAGGAGGCGTGCGGGCCGTGGGGGCTGAGGGGCAGGTGTTGGGGGCGGAATG A G FAR2P4,PLEKHB2 Ensembl:ENSG00000231431,Ensembl:ENSG00000115762 Pseudogene,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131299242..131299641 26863196 MeRIP-seq:(Medium) rs1298110098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8911,Human_RBP_ID_205861,Human_RBP_ID_264252,Human_RBP_ID_776983,Human_RBP_ID_828275,Human_RBP_ID_1592576,Human_RBP_ID_3638147,Human_RBP_ID_3959555,Human_RBP_ID_5089154,Human_RBP_ID_5146647,Human_RBP_ID_5196766,Human_RBP_ID_5322201,Human_RBP_ID_8200699,Human_RBP_ID_8728544,Human_RBP_ID_8852395,Human_RBP_ID_8942707,Human_RBP_ID_9297673,Human_RBP_ID_9341210,Human_RBP_ID_9429342,Human_RBP_ID_10001449,Human_RBP_ID_14001598,Human_RBP_ID_17141910,Human_RBP_ID_17192471,Human_RBP_ID_17208125,Human_RBP_ID_17280268,Human_RBP_ID_17393027,Human_RBP_ID_17510298,Human_RBP_ID_17670673,Human_RBP_ID_18493575,Human_RBP_ID_18950052,Human_RBP_ID_20619392,Human_RBP_ID_21980776,Human_RBP_ID_22449977,Human_RBP_ID_22596254,Human_RBP_ID_22721119,Human_RBP_ID_23282971,Human_RBP_ID_26339859,Human_RBP_ID_26787171 RMVar_hsa_circ_54692 74138 RMVar_ID_74138 Human_SNP_ID_92128214 m1A Human chr2 + 131300431 131300431 131300431 GGTACGGGCTGGTGAAAGTGGAGACGGACGGCAGGATGGATTCACTTGGCCACATGGCACGAAGC GGTACGGGCTGGTGAAAGTGGAGACGGACGGCGGGATGGATTCACTTGGCCACATGGCACGAAGC A G FAR2P4,PLEKHB2 Ensembl:ENSG00000231431,Ensembl:ENSG00000115762 Pseudogene,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:131300380..131300480 26863196 MeRIP-seq:(Medium) rs1160850196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720746,Human_RBP_ID_22996875 RMVar_hsa_circ_54692 74139 RMVar_ID_74139 Human_SNP_ID_92159930 m1A Human chr2 - 131424600 131424600 131424600 TGTATCGGAACATCTTCACGGCCATGCAGGCCATGATCAGAGCCATAGACTCACTCAAGATCCCA TGTATCGGAACATCTTCACGGCCATGCAGGCCGTGATCAGAGCCATAGACTCACTCAAGATCCCA T C GNAQP1 Ensembl:ENSG00000214077 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:131424582..131424667 26863410 MeRIP-seq:(Medium) rs1202545194 Functional Loss SNV dbSNP153 33..33 33 - - - 74140 RMVar_ID_74140 Human_SNP_ID_92176797 m1A Human chr2 - 131488652 131488652 131488652 GAGGCCACAGATGGAATGCTGAGAGCTCTCTGAGGCCCACATATTACAGCTTCTGACCACACAGA GAGGCCACAGATGGAATGCTGAGAGCTCTCTGCGGCCCACATATTACAGCTTCTGACCACACAGA T G MZT2A Ensembl:ENSG00000173272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:131488648..131489296 26863196 MeRIP-seq:(Medium) rs566668755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114413,RMVar_hsa_circ_203287 74141 RMVar_ID_74141 Human_SNP_ID_92176856 m1A Human chr2 - 131488881 131488881 131488881 AATGGGGGCTCCAAGAGAATTTACCCGAGGACAGGAGTGGCCTGGAGTGCTGGGCCCCTCAGGGT AATGGGGGCTCCAAGAGAATTTACCCGAGGACGGGAGTGGCCTGGAGTGCTGGGCCCCTCAGGGT T C MZT2A Ensembl:ENSG00000173272 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:131488871..131489046 26863196 MeRIP-seq:(Medium) rs1164120582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5147582,Human_RBP_ID_6824064,Human_RBP_ID_8202320,Human_RBP_ID_26770392 RMVar_hsa_circ_114413,RMVar_hsa_circ_203287 74142 RMVar_ID_74142 Human_SNP_ID_92177845 m1A Human chr2 - 131492023 131492023 131492023 GGCTCACCGGCCCCGCGTCTGTCCCCGCCAGGATCCTGGTGGACCTGCTGAAGCTGAACGTGGCC GGCTCACCGGCCCCGCGTCTGTCCCCGCCAGGGTCCTGGTGGACCTGCTGAAGCTGAACGTGGCC T C MZT2A Ensembl:ENSG00000173272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:131492019..131492168 26863196 MeRIP-seq:(Medium) rs755811558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_298342,Human_Splice_Rec_298350,Human_Splice_Rec_298360,Human_Splice_Rec_298366 Human_miRNA_ID_2219893,Human_miRNA_ID_2482933,Human_miRNA_ID_3071308 RMVar_hsa_circ_89439,RMVar_hsa_circ_114413,RMVar_hsa_circ_203287,RMVar_hsa_circ_203288 74143 RMVar_ID_74143 Human_SNP_ID_92177963 m1A Human chr2 + 131492245 131492245 131492245 ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGAGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGCGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:131492226..131492300 26863196 MeRIP-seq:(Medium) rs1042999 Functional Loss SNV dbSNP153 33..33 33 - - - 74144 RMVar_ID_74144 Human_SNP_ID_92177964 m1A Human chr2 + 131492245 131492245 131492245 ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGAGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGGGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:131492226..131492300 26863196 MeRIP-seq:(Medium) rs1042999 Functional Loss SNV dbSNP153 33..33 33 - - - 74145 RMVar_ID_74145 Human_SNP_ID_92177971 m1A Human chr2 - 131492265 131492259 131492265 TGCGGCGCAAGAAGGTGCTGAGCACCGAGGAGATGGAGCTGTACGAGCTGGCTCAGGCGGCGGGC TGCGGCGCAAGAAGGTGCTGAGCACCGAGGAG______CTGTACGAGCTGGCTCAGGCGGCGGGC GCTCCAT G MZT2A Ensembl:ENSG00000173272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:131492201..131492400 26863196 MeRIP-seq:(Medium) rs768597164 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_534412,Human_RBP_ID_4581691,Human_RBP_ID_9093682,Human_RBP_ID_17658184,Human_RBP_ID_22451610,Human_RBP_ID_26820176 Human_Splice_Rec_298341,Human_Splice_Rec_298349,Human_Splice_Rec_298359,Human_Splice_Rec_298365 74146 RMVar_ID_74146 Human_SNP_ID_92177974 m1A Human chr2 - 131492265 131492265 131492265 TGCGGCGCAAGAAGGTGCTGAGCACCGAGGAGATGGAGCTGTACGAGCTGGCTCAGGCGGCGGGC TGCGGCGCAAGAAGGTGCTGAGCACCGAGGAGTTGGAGCTGTACGAGCTGGCTCAGGCGGCGGGC T A MZT2A Ensembl:ENSG00000173272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:131492201..131492400 26863196 MeRIP-seq:(Medium) rs1454954510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534412,Human_RBP_ID_4581691,Human_RBP_ID_9093682,Human_RBP_ID_17658184,Human_RBP_ID_22451610,Human_RBP_ID_26820176 Human_Splice_Rec_298341,Human_Splice_Rec_298349,Human_Splice_Rec_298359,Human_Splice_Rec_298365 74147 RMVar_ID_74147 Human_SNP_ID_92178024 m1A Human chr2 + 131492343 131492342 131492343 CCGGGCCGCCTCCAGCCCCGGGGGCGCCGCCGACCCCGGCCCAGGCCCTACGCCCTGCGCCGCCA CCGGGCCGCCTCCAGCCCCGGGGGCGCCGCCG_CCCCGGCCCAGGCCCTACGCCCTGCGCCGCCA GA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr2:131492267..131492369;chr2:131492251..131492400 26863410 MeRIP-seq:(Medium) rs1205693602 Functional Loss DEL dbSNP153 33..33 33 - - - 74148 RMVar_ID_74148 Human_SNP_ID_92178027 m1A Human chr2 + 131492343 131492343 131492343 CCGGGCCGCCTCCAGCCCCGGGGGCGCCGCCGACCCCGGCCCAGGCCCTACGCCCTGCGCCGCCA CCGGGCCGCCTCCAGCCCCGGGGGCGCCGCCGCCCCCGGCCCAGGCCCTACGCCCTGCGCCGCCA A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr2:131492267..131492369;chr2:131492251..131492400 26863410 MeRIP-seq:(Medium) rs989390807 Functional Loss SNV dbSNP153 33..33 33 - - - 74149 RMVar_ID_74149 Human_SNP_ID_92178183 m1A Human chr2 + 131492613 131492613 131492613 CGTCGGGAGTGGCATGGCGGACTGCAGGGGCCAGCTGCTTGGCGGTCAGGGCGTCCCTGATAGAC CGTCGGGAGTGGCATGGCGGACTGCAGGGGCCCGCTGCTTGGCGGTCAGGGCGTCCCTGATAGAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:131492562..131492686 26863196 MeRIP-seq:(Medium) rs1261315107 Functional Loss SNV dbSNP153 33..33 33 - - - 74150 RMVar_ID_74150 Human_SNP_ID_92183855 m1A Human chr2 + 131512727 131512727 131512727 CGGCCACAGCACACGGGGGCACCTCATTCCGCAGGAGCCACTGCAGAGGAGAGGAGGAACCTGAG CGGCCACAGCACACGGGGGCACCTCATTCCGCGGGAGCCACTGCAGAGGAGAGGAGGAACCTGAG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:131512676..131512830 26863196 MeRIP-seq:(Medium) rs1410998406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3959569,Human_RBP_ID_9113752,Human_RBP_ID_17135865 RMVar_hsa_circ_35467 74151 RMVar_ID_74151 Human_SNP_ID_92248001 m1A Human chr2 - 131754403 131754403 131754403 GTCCACGGGGCCCAGTGTAGGGCCTGATGGGAAGGCACTTTCATCCGTGGGGGACCCATGCCCCG GTCCACGGGGCCCAGTGTAGGGCCTGATGGGATGGCACTTTCATCCGTGGGGGACCCATGCCCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:131754365..131754503 26863196 MeRIP-seq:(Medium) rs1397744229 Functional Loss SNV dbSNP153 33..33 33 - - - 74152 RMVar_ID_74152 Human_SNP_ID_92248002 m1A Human chr2 - 131754403 131754403 131754403 GTCCACGGGGCCCAGTGTAGGGCCTGATGGGAAGGCACTTTCATCCGTGGGGGACCCATGCCCCG GTCCACGGGGCCCAGTGTAGGGCCTGATGGGAGGGCACTTTCATCCGTGGGGGACCCATGCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:131754365..131754503 26863196 MeRIP-seq:(Medium) rs1397744229 Functional Loss SNV dbSNP153 33..33 33 - - - 74153 RMVar_ID_74153 Human_SNP_ID_92269861 m1A Human chr2 - 131829544 131829523 131829545 CGCCTGGGGCTCACGGTCCTGCGGGCCCGCCGAGGCCGCGCCCTGGGCCCGCCCCGCCCCGCAGT CGCCTGGGGCTCACGGTCCTGCGGGCCCGCC______________________CCGCCCCGCAGT GGGCGGGCCCAGGGCGCGGCCTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:131829497..131829580 26863196 MeRIP-seq:(Medium) rs932831344 Functional Loss DEL dbSNP153 32..53 33 - - - 74154 RMVar_ID_74154 Human_SNP_ID_92398096 m1A Human chr2 - 132254380 132254380 132254380 TGACTATCTAGAGGAAGTAAAAGTCGTAACAAAGTTTCGGTAGGTGAACCTGCGGAGGGATCATT TGACTATCTAGAGGAAGTAAAAGTCGTAACAAGGTTTCGGTAGGTGAACCTGCGGAGGGATCATT T C ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62164986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270137,Human_RBP_ID_280328,Human_RBP_ID_558828,Human_RBP_ID_1020181,Human_RBP_ID_1098008,Human_RBP_ID_1193005,Human_RBP_ID_1240433,Human_RBP_ID_1297279,Human_RBP_ID_1375304,Human_RBP_ID_1592643,Human_RBP_ID_1897797,Human_RBP_ID_2585922,Human_RBP_ID_3595217,Human_RBP_ID_4581797,Human_RBP_ID_5194358,Human_RBP_ID_5262229,Human_RBP_ID_5275480,Human_RBP_ID_5422298,Human_RBP_ID_5443903,Human_RBP_ID_5469902,Human_RBP_ID_5502815,Human_RBP_ID_5588520,Human_RBP_ID_6824236,Human_RBP_ID_8111306,Human_RBP_ID_8257258,Human_RBP_ID_8500974,Human_RBP_ID_8852500,Human_RBP_ID_9093698,Human_RBP_ID_9259182,Human_RBP_ID_9294881,Human_RBP_ID_9939379,Human_RBP_ID_13612566,Human_RBP_ID_17011765,Human_RBP_ID_17063456,Human_RBP_ID_17134557,Human_RBP_ID_17192604,Human_RBP_ID_17280368,Human_RBP_ID_17388824,Human_RBP_ID_17503545,Human_RBP_ID_17697257,Human_RBP_ID_17939860,Human_RBP_ID_18180751,Human_RBP_ID_18200758,Human_RBP_ID_18209113,Human_RBP_ID_18309934,Human_RBP_ID_18442480,Human_RBP_ID_18515368,Human_RBP_ID_18533276,Human_RBP_ID_18746081,Human_RBP_ID_19031420,Human_RBP_ID_20436292,Human_RBP_ID_21892950,Human_RBP_ID_21930769,Human_RBP_ID_22072594,Human_RBP_ID_22243425,Human_RBP_ID_22391870,Human_RBP_ID_22422817,Human_RBP_ID_22504449,Human_RBP_ID_22813585,Human_RBP_ID_22981686,Human_RBP_ID_23132269,Human_RBP_ID_23181751,Human_RBP_ID_23280015,Human_RBP_ID_23310367,Human_RBP_ID_23825099,Human_RBP_ID_24486064,Human_RBP_ID_24533266,Human_RBP_ID_24538954,Human_RBP_ID_24540220,Human_RBP_ID_25462185,Human_RBP_ID_26476947,Human_RBP_ID_26657147,Human_RBP_ID_26749713,Human_RBP_ID_27000759,Human_RBP_ID_27158156,Human_RBP_ID_27282827,Human_RBP_ID_27474939,Human_RBP_ID_27563148,Human_RBP_ID_27686734 74155 RMVar_ID_74155 Human_SNP_ID_92398600 m1A Human chr2 - 132255511 132255511 132255511 TAAAGTTGTTGCAGTTAAAAAGCTCGTAGTTGAATCTTGGGAGCGGGTGGGCTAGCGAGCCACAG TAAAGTTGTTGCAGTTAAAAAGCTCGTAGTTGGATCTTGGGAGCGGGTGGGCTAGCGAGCCACAG T C ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs77190340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270152,Human_RBP_ID_280349,Human_RBP_ID_1020202,Human_RBP_ID_1095626,Human_RBP_ID_1197378,Human_RBP_ID_1240442,Human_RBP_ID_1297297,Human_RBP_ID_1375328,Human_RBP_ID_1592654,Human_RBP_ID_2671703,Human_RBP_ID_4581821,Human_RBP_ID_5194377,Human_RBP_ID_5262254,Human_RBP_ID_5422339,Human_RBP_ID_5443937,Human_RBP_ID_5469949,Human_RBP_ID_5500910,Human_RBP_ID_5594699,Human_RBP_ID_6824319,Human_RBP_ID_8104463,Human_RBP_ID_8257282,Human_RBP_ID_8501008,Human_RBP_ID_8842330,Human_RBP_ID_9093739,Human_RBP_ID_9259191,Human_RBP_ID_9294889,Human_RBP_ID_10001995,Human_RBP_ID_13612653,Human_RBP_ID_17011792,Human_RBP_ID_17068632,Human_RBP_ID_17192619,Human_RBP_ID_17273597,Human_RBP_ID_17388845,Human_RBP_ID_17503593,Human_RBP_ID_17697291,Human_RBP_ID_17939902,Human_RBP_ID_18179993,Human_RBP_ID_18200787,Human_RBP_ID_18208759,Human_RBP_ID_18309957,Human_RBP_ID_18442497,Human_RBP_ID_18515383,Human_RBP_ID_18533294,Human_RBP_ID_18768318,Human_RBP_ID_19031603,Human_RBP_ID_20436301,Human_RBP_ID_21892961,Human_RBP_ID_21930788,Human_RBP_ID_22005653,Human_RBP_ID_22072616,Human_RBP_ID_22243445,Human_RBP_ID_22391878,Human_RBP_ID_22422585,Human_RBP_ID_22504471,Human_RBP_ID_22813610,Human_RBP_ID_22997892,Human_RBP_ID_23132293,Human_RBP_ID_23283302,Human_RBP_ID_23310380,Human_RBP_ID_24533282,Human_RBP_ID_24538962,Human_RBP_ID_24540232,Human_RBP_ID_25462217,Human_RBP_ID_26476987,Human_RBP_ID_26657167,Human_RBP_ID_26749746,Human_RBP_ID_27000780,Human_RBP_ID_27158192,Human_RBP_ID_27282861,Human_RBP_ID_27474986,Human_RBP_ID_27563176,Human_RBP_ID_27686750 74156 RMVar_ID_74156 Human_SNP_ID_92398637 m1A Human chr2 - 132255602 132255602 132255602 ATGAGTGCACTTTAAATCTTTTAATGAGGATCAATTGGAGGGCAAGTCTGGTGCCAGCAGCCGTG ATGAGTGCACTTTAAATCTTTTAATGAGGATCCATTGGAGGGCAAGTCTGGTGCCAGCAGCCGTG T G ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62165000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270155,Human_RBP_ID_280349,Human_RBP_ID_1020202,Human_RBP_ID_1897819,Human_RBP_ID_2671705,Human_RBP_ID_3595236,Human_RBP_ID_4581821,Human_RBP_ID_5194379,Human_RBP_ID_5262254,Human_RBP_ID_5422339,Human_RBP_ID_5443937,Human_RBP_ID_5469950,Human_RBP_ID_5500911,Human_RBP_ID_6824321,Human_RBP_ID_8104465,Human_RBP_ID_8257283,Human_RBP_ID_8501009,Human_RBP_ID_8842330,Human_RBP_ID_9093743,Human_RBP_ID_13612655,Human_RBP_ID_17011797,Human_RBP_ID_17063485,Human_RBP_ID_17273600,Human_RBP_ID_17388845,Human_RBP_ID_17503598,Human_RBP_ID_17697291,Human_RBP_ID_17939904,Human_RBP_ID_18200788,Human_RBP_ID_18208759,Human_RBP_ID_18309958,Human_RBP_ID_18442499,Human_RBP_ID_18515383,Human_RBP_ID_18533294,Human_RBP_ID_21892963,Human_RBP_ID_21930790,Human_RBP_ID_22422585,Human_RBP_ID_22451613,Human_RBP_ID_22504472,Human_RBP_ID_22813616,Human_RBP_ID_23132296,Human_RBP_ID_23280041,Human_RBP_ID_23311042,Human_RBP_ID_23825161,Human_RBP_ID_24423926,Human_RBP_ID_24490712,Human_RBP_ID_24533282,Human_RBP_ID_24538964,Human_RBP_ID_24540234,Human_RBP_ID_26476990,Human_RBP_ID_26749747,Human_RBP_ID_27282861,Human_RBP_ID_27474986,Human_RBP_ID_27563176,Human_RBP_ID_27840109 74157 RMVar_ID_74157 Human_SNP_ID_92404794 m1A Human chr2 + 132266774 132266774 132266774 AGAGAGAGATAGACAGACAGGCAGAGAAAGACAGTAAGACAGAAGACAGACAAAGAGAGAGAGAG AGAGAGAGATAGACAGACAGGCAGAGAAAGACGGTAAGACAGAAGACAGACAAAGAGAGAGAGAG A G lnc-GPR39-10,lnc-GPR39-10:2 RNACentral:URS0000D5BB06,RNACentral:URS0000D59EB8 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:132266764..132266829 26863196 MeRIP-seq:(Medium) rs1027947805 Functional Loss SNV dbSNP153 33..33 33 - - - 74158 RMVar_ID_74158 Human_SNP_ID_92406664 m1A Human chr2 + 132269695 132269695 132269695 GATAGGCAGAGAAAGAGAGTAAGACAGAAGACAGATACAGTGAGAGAGACAGGCAGAGAGAGACA GATAGGCAGAGAAAGAGAGTAAGACAGAAGACCGATACAGTGAGAGAGACAGGCAGAGAGAGACA A C lnc-GPR39-10,lnc-GPR39-10:2 RNACentral:URS0000D5BB06,RNACentral:URS0000D59EB8 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:132269675..132269774 26863196 MeRIP-seq:(Medium) rs796851282 Functional Loss SNV dbSNP153 33..33 33 - - - 74159 RMVar_ID_74159 Human_SNP_ID_92412837 m1A Human chr2 - 132280615 132280615 132280615 CAGACTCTGGCATGTTGGAACAATGTAGGTAAAGGAAGTCCTCAAGCCGGATCCATAACTTCGGG CAGACTCTGGCATGTTGGAACAATGTAGGTAAGGGAAGTCCTCAAGCCGGATCCATAACTTCGGG T C RF02543-029,RF02543-030 RNACentral:URS000096B970,RNACentral:URS00008D183F rRNA,rRNA exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs76637258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270169,Human_RBP_ID_280363,Human_RBP_ID_1020217,Human_RBP_ID_1095643,Human_RBP_ID_1133734,Human_RBP_ID_1197380,Human_RBP_ID_1240453,Human_RBP_ID_1297319,Human_RBP_ID_1379503,Human_RBP_ID_1592662,Human_RBP_ID_1897829,Human_RBP_ID_2671774,Human_RBP_ID_3595249,Human_RBP_ID_4627316,Human_RBP_ID_5194410,Human_RBP_ID_5262269,Human_RBP_ID_5275643,Human_RBP_ID_5423409,Human_RBP_ID_5445295,Human_RBP_ID_5471544,Human_RBP_ID_5500945,Human_RBP_ID_5588558,Human_RBP_ID_6824384,Human_RBP_ID_8104477,Human_RBP_ID_8257301,Human_RBP_ID_8501045,Human_RBP_ID_8842365,Human_RBP_ID_9093769,Human_RBP_ID_9259200,Human_RBP_ID_9294896,Human_RBP_ID_9939410,Human_RBP_ID_14005410,Human_RBP_ID_17017820,Human_RBP_ID_17068835,Human_RBP_ID_17191237,Human_RBP_ID_17280376,Human_RBP_ID_17388863,Human_RBP_ID_17503620,Human_RBP_ID_17697332,Human_RBP_ID_17939940,Human_RBP_ID_18179997,Human_RBP_ID_18200801,Human_RBP_ID_18208775,Human_RBP_ID_18309973,Human_RBP_ID_18442511,Human_RBP_ID_18515395,Human_RBP_ID_18533303,Human_RBP_ID_18746134,Human_RBP_ID_20436340,Human_RBP_ID_21892970,Human_RBP_ID_21930801,Human_RBP_ID_22243483,Human_RBP_ID_22422828,Human_RBP_ID_22504483,Human_RBP_ID_22813659,Human_RBP_ID_22997909,Human_RBP_ID_23133353,Human_RBP_ID_23181790,Human_RBP_ID_23280060,Human_RBP_ID_23310402,Human_RBP_ID_23892753,Human_RBP_ID_24533291,Human_RBP_ID_24538968,Human_RBP_ID_24540241,Human_RBP_ID_25462254,Human_RBP_ID_26477008,Human_RBP_ID_26657183,Human_RBP_ID_26749772,Human_RBP_ID_27000836,Human_RBP_ID_27158268,Human_RBP_ID_27294051,Human_RBP_ID_27475033,Human_RBP_ID_27563197,Human_RBP_ID_27686759 74160 RMVar_ID_74160 Human_SNP_ID_92412838 m1A Human chr2 - 132280615 132280615 132280615 CAGACTCTGGCATGTTGGAACAATGTAGGTAAAGGAAGTCCTCAAGCCGGATCCATAACTTCGGG CAGACTCTGGCATGTTGGAACAATGTAGGTAACGGAAGTCCTCAAGCCGGATCCATAACTTCGGG T G RF02543-029,RF02543-030 RNACentral:URS000096B970,RNACentral:URS00008D183F rRNA,rRNA exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs76637258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270169,Human_RBP_ID_280363,Human_RBP_ID_1020217,Human_RBP_ID_1095643,Human_RBP_ID_1133734,Human_RBP_ID_1197380,Human_RBP_ID_1240453,Human_RBP_ID_1297319,Human_RBP_ID_1379503,Human_RBP_ID_1592662,Human_RBP_ID_1897829,Human_RBP_ID_2671774,Human_RBP_ID_3595249,Human_RBP_ID_4627316,Human_RBP_ID_5194410,Human_RBP_ID_5262269,Human_RBP_ID_5275643,Human_RBP_ID_5423409,Human_RBP_ID_5445295,Human_RBP_ID_5471544,Human_RBP_ID_5500945,Human_RBP_ID_5588558,Human_RBP_ID_6824384,Human_RBP_ID_8104477,Human_RBP_ID_8257301,Human_RBP_ID_8501045,Human_RBP_ID_8842365,Human_RBP_ID_9093769,Human_RBP_ID_9259200,Human_RBP_ID_9294896,Human_RBP_ID_9939410,Human_RBP_ID_14005410,Human_RBP_ID_17017820,Human_RBP_ID_17068835,Human_RBP_ID_17191237,Human_RBP_ID_17280376,Human_RBP_ID_17388863,Human_RBP_ID_17503620,Human_RBP_ID_17697332,Human_RBP_ID_17939940,Human_RBP_ID_18179997,Human_RBP_ID_18200801,Human_RBP_ID_18208775,Human_RBP_ID_18309973,Human_RBP_ID_18442511,Human_RBP_ID_18515395,Human_RBP_ID_18533303,Human_RBP_ID_18746134,Human_RBP_ID_20436340,Human_RBP_ID_21892970,Human_RBP_ID_21930801,Human_RBP_ID_22243483,Human_RBP_ID_22422828,Human_RBP_ID_22504483,Human_RBP_ID_22813659,Human_RBP_ID_22997909,Human_RBP_ID_23133353,Human_RBP_ID_23181790,Human_RBP_ID_23280060,Human_RBP_ID_23310402,Human_RBP_ID_23892753,Human_RBP_ID_24533291,Human_RBP_ID_24538968,Human_RBP_ID_24540241,Human_RBP_ID_25462254,Human_RBP_ID_26477008,Human_RBP_ID_26657183,Human_RBP_ID_26749772,Human_RBP_ID_27000836,Human_RBP_ID_27158268,Human_RBP_ID_27294051,Human_RBP_ID_27475033,Human_RBP_ID_27563197,Human_RBP_ID_27686759 74161 RMVar_ID_74161 Human_SNP_ID_92413075 m1A Human chr2 + 132281092 132281092 132281092 GTTCAACTGCTGTTCACATGGAACCCTTCTCCACTTCGGCCTTCAAAGTTCTCATTTGAAAATTT GTTCAACTGCTGTTCACATGGAACCCTTCTCCTCTTCGGCCTTCAAAGTTCTCATTTGAAAATTT A T lnc-GPR39-10,lnc-GPR39-7 RNACentral:URS0000D5BB06,RNACentral:URS00008B47C3 lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:132281049..132281153 26863196 MeRIP-seq:(Medium) rs1216601215 Functional Loss SNV dbSNP153 33..33 33 - - - 74162 RMVar_ID_74162 Human_SNP_ID_92413082 m1A Human chr2 + 132281104 132281104 132281104 TTCACATGGAACCCTTCTCCACTTCGGCCTTCAAAGTTCTCATTTGAAAATTTGCTACTACCACC TTCACATGGAACCCTTCTCCACTTCGGCCTTCCAAGTTCTCATTTGAAAATTTGCTACTACCACC A C lnc-GPR39-10,lnc-GPR39-7 RNACentral:URS0000D5BB06,RNACentral:URS00008B47C3 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:132281076..132281150 26863196 MeRIP-seq:(Medium) rs541415909 Functional Loss SNV dbSNP153 33..33 33 - - - 74163 RMVar_ID_74163 Human_SNP_ID_92413083 m1A Human chr2 + 132281104 132281104 132281104 TTCACATGGAACCCTTCTCCACTTCGGCCTTCAAAGTTCTCATTTGAAAATTTGCTACTACCACC TTCACATGGAACCCTTCTCCACTTCGGCCTTCGAAGTTCTCATTTGAAAATTTGCTACTACCACC A G lnc-GPR39-10,lnc-GPR39-7 RNACentral:URS0000D5BB06,RNACentral:URS00008B47C3 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:132281076..132281150 26863196 MeRIP-seq:(Medium) rs541415909 Functional Loss SNV dbSNP153 33..33 33 - - - 74164 RMVar_ID_74164 Human_SNP_ID_92413351 m1A Human chr2 + 132281551 132281551 132281551 GTTCATCCCACAGTGCCAGTTCTGCTTACCAAAAGTAGCCTACGAAGCACTCGCATTCCACGCCT GTTCATCCCACAGTGCCAGTTCTGCTTACCAACAGTAGCCTACGAAGCACTCGCATTCCACGCCT A C lnc-GPR39-10 RNACentral:URS0000D5BB06 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:132281526..132281550 26863196 MeRIP-seq:(Medium) rs540826380 Functional Loss SNV dbSNP153 33..33 33 - - - 74165 RMVar_ID_74165 Human_SNP_ID_92429412 m1A Human chr2 - 132345900 132345900 132345900 AAACAGTTGGGAGAGTCATGCATTTGGGGCTAATTTTCTCCTGGGGATGATGGTCTAGTCTAGGA AAACAGTTGGGAGAGTCATGCATTTGGGGCTACTTTTCTCCTGGGGATGATGGTCTAGTCTAGGA T G AC097532.2 Ensembl:ENSG00000272769 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4954309 Functional Loss SNV dbSNP153 33..33 33 - - - 74166 RMVar_ID_74166 Human_SNP_ID_92503798 m1A Human chr2 + 132645117 132645117 132645117 GCTCGTGTCTGCCCAGGGCTGATTGTTGTGACATTGGCCGTATGCTGGATGCCCAACCAGATTCG GCTCGTGTCTGCCCAGGGCTGATTGTTGTGACGTTGGCCGTATGCTGGATGCCCAACCAGATTCG A G GPR39 Ensembl:ENSG00000183840 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:132645066..132645161 26863196 MeRIP-seq:(Medium) rs752927626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_298702,Human_Splice_Rec_298708 74167 RMVar_ID_74167 Human_SNP_ID_92510595 m1A Human chr2 - 132670103 132670103 132670103 CCCGCAGCCGGGAGCCCGAGCGCGGGCGATGCAGGCTCCGCGAGCGGCACCTGCGGCTCCTCTAA CCCGCAGCCGGGAGCCCGAGCGCGGGCGATGCCGGCTCCGCGAGCGGCACCTGCGGCTCCTCTAA T G LYPD1 Ensembl:ENSG00000150551 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:132670065..132670240 26863196 MeRIP-seq:(Medium) rs1553465934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4627354 74168 RMVar_ID_74168 Human_SNP_ID_92510952 m1A Human chr2 - 132671376 132671376 132671376 CCCCCAGAAGTGGCCGGGGGAGAAAAGGGTGAAGAGGAGCTAAAGCTTAGGAGGCGATTTCCACG CCCCCAGAAGTGGCCGGGGGAGAAAAGGGTGACGAGGAGCTAAAGCTTAGGAGGCGATTTCCACG T G LYPD1 Ensembl:ENSG00000150551 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:132671327..132671485 26863196 MeRIP-seq:(Medium) rs62178528 Functional Loss SNV dbSNP153 33..33 33 - - - 74169 RMVar_ID_74169 Human_SNP_ID_92651128 m1A Human chr2 + 133266654 133266654 133266654 CAGAGCCGGGAGTTGCCAAACTTGCCATGTCCAGAGCGCGGAGGCAGCCTGGGCCACGCGCTCAC CAGAGCCGGGAGTTGCCAAACTTGCCATGTCCTGAGCGCGGAGGCAGCCTGGGCCACGCGCTCAC A T NCKAP5-AS2 Ensembl:ENSG00000226953 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:133266610..133266713 32194978 MeRIP-seq:(Medium) rs1444003903 Functional Loss SNV dbSNP153 33..33 33 - - - 74170 RMVar_ID_74170 Human_SNP_ID_92879604 m1A Human chr2 - 134220672 134220672 134220672 AAGGCTGATCCCTGCTACAGAAAGCAAAAAACAGCAGCAGCGTGCATACACATACACATACGCAC AAGGCTGATCCCTGCTACAGAAAGCAAAAAACTGCAGCAGCGTGCATACACATACACATACGCAC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:134220669..134220796 26863196 MeRIP-seq:(Medium) rs999827910 Functional Loss SNV dbSNP153 33..33 33 - - - 74171 RMVar_ID_74171 Human_SNP_ID_93040496 m1A Human chr2 + 134918664 134918664 134918664 CCCGTGCGCAAGAGCGAGGCCGAGGGCAGAAAAAGAAAGCAAAAGACTAGGGCGAGTCGGTAGAG CCCGTGCGCAAGAGCGAGGCCGAGGGCAGAAATAGAAAGCAAAAGACTAGGGCGAGTCGGTAGAG A T CCNT2 Ensembl:ENSG00000082258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:134918613..134918765 26863196 MeRIP-seq:(Medium) rs1240326286 Functional Loss SNV dbSNP153 33..33 33 - - - 74172 RMVar_ID_74172 Human_SNP_ID_93040502 m1A Human chr2 + 134918673 134918673 134918673 AAGAGCGAGGCCGAGGGCAGAAAAAGAAAGCAAAAGACTAGGGCGAGTCGGTAGAGCGGGCCCCG AAGAGCGAGGCCGAGGGCAGAAAAAGAAAGCAGAAGACTAGGGCGAGTCGGTAGAGCGGGCCCCG A G CCNT2 Ensembl:ENSG00000082258 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:134918613..134918927 26863196 MeRIP-seq:(Medium) rs530083292 Functional Loss SNV dbSNP153 33..33 33 - - - 74173 RMVar_ID_74173 Human_SNP_ID_93047344 m1A Human chr2 + 134945280 134945280 134945280 TTAGAGGGGTGGAGTTGAGATAAACTGATCCTAGGTGAGCAGAGGGGAAAGATATGTCAGTGCTT TTAGAGGGGTGGAGTTGAGATAAACTGATCCTCGGTGAGCAGAGGGGAAAGATATGTCAGTGCTT A C CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:134945231..134945329 26863196 MeRIP-seq:(Medium) rs897109714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6825122,Human_RBP_ID_13614657 RMVar_hsa_circ_224,RMVar_hsa_circ_203356,RMVar_hsa_circ_290273,RMVar_hsa_circ_359432,RMVar_hsa_circ_203357,RMVar_hsa_circ_122916,RMVar_hsa_circ_277311,RMVar_hsa_circ_203358,RMVar_hsa_circ_203359,RMVar_hsa_circ_104550,RMVar_hsa_circ_352407,RMVar_hsa_circ_203360,RMVar_hsa_circ_203361 74174 RMVar_ID_74174 Human_SNP_ID_174554512 m1A Human chr4 - 15002541 15002540 15002541 AGTCAGTGAGAGAGGGACACCGTGACTGAGCCAGGGGGCACCGACTTCGGCCCCACCACCCCTCG AGTCAGTGAGAGAGGGACACCGTGACTGAGCC_GGGGGCACCGACTTCGGCCCCACCACCCCTCG CT C CPEB2-DT,CPEB2-DT:2,CPEB2-DT:3,CPEB2-DT:4,CPEB2-DT:5,CPEB2-DT:6 RNACentral:URS0000D5CFCA,RNACentral:URS0000D59752,RNACentral:URS0000D5C266,RNACentral:URS0000D5BB7F,RNACentral:URS0000D57253,RNACentral:URS0000D5D2E4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:15002495..15002621 26863196 MeRIP-seq:(Medium) rs1203747440 Functional Loss DEL dbSNP153 33..33 33 - - - 74175 RMVar_ID_74175 Human_SNP_ID_174554939 m1A Human chr4 - 15003233 15003221 15003234 GCGGCGGCGGCTTCGAGTCCGGAGGGTGGGGAAGGTGGGGAGGGCTGAACTCTTTCCTCTTCTGG GCGGCGGCGGCTTCGAGTCCGGAGGGTGGGG_____________CTGAACTCTTTCCTCTTCTGG GCCCTCCCCACCTT G CPEB2-DT,CPEB2-DT:2 RNACentral:URS0000D59752,RNACentral:URS0000D5C266 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:15003187..15003550 26863196 MeRIP-seq:(Medium) rs1318028196 Functional Loss DEL dbSNP153 32..44 33 - - - 74176 RMVar_ID_74176 Human_SNP_ID_174554951 m1A Human chr4 - 15003243 15003243 15003243 GGCGGAGGCGGCGGCGGCGGCTTCGAGTCCGGAGGGTGGGGAAGGTGGGGAGGGCTGAACTCTTT GGCGGAGGCGGCGGCGGCGGCTTCGAGTCCGGCGGGTGGGGAAGGTGGGGAGGGCTGAACTCTTT T G CPEB2-DT,CPEB2-DT:2 RNACentral:URS0000D59752,RNACentral:URS0000D5C266 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15003196..15003608 26863196 MeRIP-seq:(Medium) rs1157193598 Functional Loss SNV dbSNP153 33..33 33 - - - 74177 RMVar_ID_74177 Human_SNP_ID_174554954 m1A Human chr4 + 15003248 15003248 15003248 GTTCAGCCCTCCCCACCTTCCCCACCCTCCGGACTCGAAGCCGCCGCCGCCGCCTCCGCCGCTCC GTTCAGCCCTCCCCACCTTCCCCACCCTCCGGCCTCGAAGCCGCCGCCGCCGCCTCCGCCGCTCC A C CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:15003211..15003368 26863196 MeRIP-seq:(Medium) rs1312328628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27506741 74178 RMVar_ID_74178 Human_SNP_ID_174554955 m1A Human chr4 - 15003250 15003250 15003250 GTGGAGCGGCGGAGGCGGCGGCGGCGGCTTCGAGTCCGGAGGGTGGGGAAGGTGGGGAGGGCTGA GTGGAGCGGCGGAGGCGGCGGCGGCGGCTTCGGGTCCGGAGGGTGGGGAAGGTGGGGAGGGCTGA T C CPEB2-DT,CPEB2-DT:2 RNACentral:URS0000D59752,RNACentral:URS0000D5C266 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:15003200..15004069;chr4:15003200..15003491 26863196 MeRIP-seq:(Medium) rs1373746680 Functional Loss SNV dbSNP153 33..33 33 - - - 74179 RMVar_ID_74179 Human_SNP_ID_174555182 m1A Human chr4 + 15003629 15003629 15003629 CCCCGCGCCGGGCTCCATGGAGTCCCCCAACCACCCTCTGCTCAACAGTCCCAGTAACCTCCTGC CCCCGCGCCGGGCTCCATGGAGTCCCCCAACCTCCCTCTGCTCAACAGTCCCAGTAACCTCCTGC A T CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:15003578..15003700 26863196 MeRIP-seq:(Medium) rs1442517917 Functional Loss SNV dbSNP153 33..33 33 - - - 74180 RMVar_ID_74180 Human_SNP_ID_174555367 m1A Human chr4 + 15003905 15003893 15003905 CCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCAGCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT CCAGCCGCAGCAGCAGCCGCC____________GCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT CGCCACCCCAGCA C CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15003854..15004057 26863196 MeRIP-seq:(Medium) rs1472954672 Functional Loss DEL dbSNP153 22..33 33 - - - 74181 RMVar_ID_74181 Human_SNP_ID_174555374 m1A Human chr4 + 15003902 15003902 15003902 GACCCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCAGCCGCCCCAGCCGCAGCCGCAGCCGCCCG GACCCAGCCGCAGCAGCAGCCGCCGCCACCCCGGCAGCCGCCCCAGCCGCAGCCGCAGCCGCCCG A G CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:15003861..15004071 26863196 MeRIP-seq:(Medium) rs1349496858 Functional Loss SNV dbSNP153 33..33 33 - - - 74182 RMVar_ID_74182 Human_SNP_ID_174555377 m1A Human chr4 + 15003905 15003905 15003905 CCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCAGCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT CCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCCGCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT A C CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15003854..15004057 26863196 MeRIP-seq:(Medium) rs1243237611 Functional Loss SNV dbSNP153 33..33 33 - - - 74183 RMVar_ID_74183 Human_SNP_ID_174555378 m1A Human chr4 + 15003905 15003905 15003905 CCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCAGCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT CCAGCCGCAGCAGCAGCCGCCGCCACCCCAGCGGCCGCCCCAGCCGCAGCCGCAGCCGCCCGGCT A G CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15003854..15004057 26863196 MeRIP-seq:(Medium) rs1243237611 Functional Loss SNV dbSNP153 33..33 33 - - - 74184 RMVar_ID_74184 Human_SNP_ID_174555459 m1A Human chr4 + 15004013 15004013 15004013 CGCCATGCCGCCGCCCAGCCCCGACTCAGAGAACGGCTTCTACCCCGGGCTGCCGTCGTCCATGA CGCCATGCCGCCGCCCAGCCCCGACTCAGAGAGCGGCTTCTACCCCGGGCTGCCGTCGTCCATGA A G CPEB2 Ensembl:ENSG00000137449 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:15003771..15004042 26863196 MeRIP-seq:(Medium) rs757353466 Functional Loss SNV dbSNP153 33..33 33 - - - 74185 RMVar_ID_74185 Human_SNP_ID_174555469 m1A Human chr4 - 15004031 15004031 15004031 TAGGGAAGAAGGCCGGGTTCATGGACGACGGCAGCCCGGGGTAGAAGCCGTTCTCTGAGTCGGGG TAGGGAAGAAGGCCGGGTTCATGGACGACGGCGGCCCGGGGTAGAAGCCGTTCTCTGAGTCGGGG T C CPEB2-DT,CPEB2-DT:2 RNACentral:URS0000D59752,RNACentral:URS0000D5C266 lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:15003725..15004075 26863196 MeRIP-seq:(Medium) rs774517467 Functional Loss SNV dbSNP153 33..33 33 - - - 74186 RMVar_ID_74186 Human_SNP_ID_174721946 m1A Human chr4 - 15681840 15681840 15681840 GCCCAGCGCTGCAAGCCTCAGGTCTCTCCAGCAGAGCTGCGCCTCTGCTCTCCCCACACTTCCCT GCCCAGCGCTGCAAGCCTCAGGTCTCTCCAGCGGAGCTGCGCCTCTGCTCTCCCCACACTTCCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:15681760..15682000 26863196 MeRIP-seq:(Medium) rs1463380356 Functional Loss SNV dbSNP153 33..33 33 - - - 74187 RMVar_ID_74187 Human_SNP_ID_174727807 m1A Human chr4 + 15703885 15703885 15703885 GAGGGGTGTGTGCATGTGTGTTCTAGAGGTGAAGGGGGTGTGTGTGCGTGCGCTCTAGAGGTGAG GAGGGGTGTGTGCATGTGTGTTCTAGAGGTGAGGGGGGTGTGTGTGCGTGCGCTCTAGAGGTGAG A G FAM200B,BST1 Ensembl:ENSG00000237765,Ensembl:ENSG00000109743 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:15703802..15703965 26863196 MeRIP-seq:(Medium) rs1301492883 Functional Loss SNV dbSNP153 33..33 33 - - - 74188 RMVar_ID_74188 Human_SNP_ID_174727815 m1A Human chr4 - 15703901 15703900 15703901 TAGAATACACACACCCCTCACCTCTAGAGCGCACGCACACACACCCCCTTCACCTCTAGAACACA TAGAATACACACACCCCTCACCTCTAGAGCGC_CGCACACACACCCCCTTCACCTCTAGAACACA GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15703718..15703958 26863196 MeRIP-seq:(Medium) rs1560275070 Functional Loss DEL dbSNP153 33..33 33 - - - 74189 RMVar_ID_74189 Human_SNP_ID_174727816 m1A Human chr4 - 15703901 15703901 15703901 TAGAATACACACACCCCTCACCTCTAGAGCGCACGCACACACACCCCCTTCACCTCTAGAACACA TAGAATACACACACCCCTCACCTCTAGAGCGCGCGCACACACACCCCCTTCACCTCTAGAACACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15703718..15703958 26863196 MeRIP-seq:(Medium) rs1206933838 Functional Loss SNV dbSNP153 33..33 33 - - - 74190 RMVar_ID_74190 Human_SNP_ID_174786868 m1A Human chr4 - 15936568 15936568 15936568 CCTCCTACTGGCTGCTCAGGTGCTCCTGGTGGAGGGGAAAAAAAAAGTGAAGAATGGACTTCACA CCTCCTACTGGCTGCTCAGGTGCTCCTGGTGGGGGGGAAAAAAAAAGTGAAGAATGGACTTCACA T C FGFBP1 Ensembl:ENSG00000137440 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:15936518..15936663 26863196 MeRIP-seq:(Medium) rs763857437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_547946 RMVar_hsa_circ_108131,RMVar_hsa_circ_118360,RMVar_hsa_circ_224917,RMVar_hsa_circ_224918 74191 RMVar_ID_74191 Human_SNP_ID_174786906 m1A Human chr4 - 15936649 15936649 15936649 CACTGACTCACTTGCCTTTTGTCAAACAGGTGAACGCCCAGCTGCAGCCATGAAGATCTGTAGCC CACTGACTCACTTGCCTTTTGTCAAACAGGTGGACGCCCAGCTGCAGCCATGAAGATCTGTAGCC T C FGFBP1 Ensembl:ENSG00000137440 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:15936450..15936681 26863196 MeRIP-seq:(Medium) rs775689425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_547946 RMVar_hsa_circ_108131,RMVar_hsa_circ_118360,RMVar_hsa_circ_224917,RMVar_hsa_circ_224918 74192 RMVar_ID_74192 Human_SNP_ID_174843953 m1A Human chr4 + 16162183 16162183 16162183 ACCCATACGCCTCAAACACCCCATTTACTTTCACACAAAATCCTCTCCAGACCCAGGCCTGCCCC ACCCATACGCCTCAAACACCCCATTTACTTTCGCACAAAATCCTCTCCAGACCCAGGCCTGCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:16162115..16162337 26863196 MeRIP-seq:(Medium) rs1378339947 Functional Loss SNV dbSNP153 33..33 33 - - - 74193 RMVar_ID_74193 Human_SNP_ID_174845722 m1A Human chr4 - 16168495 16168495 16168495 AGGGCATGGGGACACAGGCCTGATGGAGGAACAGCAGGCACCAGGCAGCTGCAGTAGTCCATGAG AGGGCATGGGGACACAGGCCTGATGGAGGAACCGCAGGCACCAGGCAGCTGCAGTAGTCCATGAG T G TAPT1 Ensembl:ENSG00000169762 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:16168368..16168568 26863196 MeRIP-seq:(Medium) rs1314219876 Functional Loss SNV dbSNP153 33..33 33 - - - 74194 RMVar_ID_74194 Human_SNP_ID_174857438 m1A Human chr4 + 16216654 16216654 16216654 GGGCCAATCTTGACAATCCCCTCTCTCTTCTTACCAAGGTCTACCAATTCTTCCTTTAAAACATT GGGCCAATCTTGACAATCCCCTCTCTCTTCTTCCCAAGGTCTACCAATTCTTCCTTTAAAACATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:16216643..16216743 26863196 MeRIP-seq:(Medium) rs1006163887 Functional Loss SNV dbSNP153 33..33 33 - - - 74195 RMVar_ID_74195 Human_SNP_ID_174857443 m1A Human chr4 - 16216673 16216673 16216673 GAAAAAGGGGAAAAAAGTTAATGTTTTAAAGGAAGAATTGGTAGACCTTGGTAAGAAGAGAGAGG GAAAAAGGGGAAAAAAGTTAATGTTTTAAAGGCAGAATTGGTAGACCTTGGTAAGAAGAGAGAGG T G TAPT1 Ensembl:ENSG00000169762 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:16216670..16216805 26863196 MeRIP-seq:(Medium) rs1449318514 Functional Loss SNV dbSNP153 33..33 33 - - - 74196 RMVar_ID_74196 Human_SNP_ID_174860021 m1A Human chr4 - 16226717 16226717 16226717 CATGGAGCCCGGCGCGGTGCCCCGGCCGGCCGAGCCAGCCACGGCGCGAGAAACCGTCGCCCGCC CATGGAGCCCGGCGCGGTGCCCCGGCCGGCCGCGCCAGCCACGGCGCGAGAAACCGTCGCCCGCC T G TAPT1 Ensembl:ENSG00000169762 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:16226679..16226981 26863196 MeRIP-seq:(Medium) rs1301140081 Functional Loss SNV dbSNP153 33..33 33 - - - 74197 RMVar_ID_74197 Human_SNP_ID_174862124 m1A Human chr4 - 16234485 16234484 16234485 TCTTCCTACCTCTCTCATTCTGCCCGTGCCCCAGCACCCACCCGTCAGGCCCTTCAGTTGCCGTC TCTTCCTACCTCTCTCATTCTGCCCGTGCCCC_GCACCCACCCGTCAGGCCCTTCAGTTGCCGTC CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:16234440..16234615 26863196 MeRIP-seq:(Medium) rs1329155235 Functional Loss DEL dbSNP153 33..33 33 - - - 74198 RMVar_ID_74198 Human_SNP_ID_175173429 m1A Human chr4 - 17501841 17501841 17501841 TTTTTTTCACTCAGCTCTCTTTAAGAACTGTGACCTGATGTGGAAGCAGAGCATATGGACATCGA TTTTTTTCACTCAGCTCTCTTTAAGAACTGTGGCCTGATGTGGAAGCAGAGCATATGGACATCGA T C QDPR Ensembl:ENSG00000151552 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:17501701..17501907 26863196 MeRIP-seq:(Medium) rs1269736545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1974807 Human_Splice_Rec_548704,Human_Splice_Rec_548716,Human_Splice_Rec_548728,Human_Splice_Rec_548736,Human_Splice_Rec_548752,Human_Splice_Rec_548762,Human_Splice_Rec_548772 RMVar_hsa_circ_54463,RMVar_hsa_circ_121417,RMVar_hsa_circ_53025,RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_224968,RMVar_hsa_circ_284056,RMVar_hsa_circ_224967,RMVar_hsa_circ_349444,RMVar_hsa_circ_224969 74199 RMVar_ID_74199 Human_SNP_ID_175176043 m1A Human chr4 + 17511948 17511948 17511948 GCGGAGACCCAGCAGCCCCAGCCCGCAGCATTACCCAGTTGCGGGCCCGAAAAGCCTGCACGCAT GCGGAGACCCAGCAGCCCCAGCCCGCAGCATTTCCCAGTTGCGGGCCCGAAAAGCCTGCACGCAT A T lnc-CLRN2-1 RNACentral:URS00008B79B6 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:17511938..17512087 26863196 MeRIP-seq:(Medium) rs1254995369 Functional Loss SNV dbSNP153 33..33 33 - - - 74200 RMVar_ID_74200 Human_SNP_ID_175176095 m1A Human chr4 + 17512037 17512037 17512037 CCGTACACCAGCACCCGGCGCGCCTCGCCTGCAGCCGCCGCCGCCGCCATCCTGCTCCTGCCAGC CCGTACACCAGCACCCGGCGCGCCTCGCCTGCCGCCGCCGCCGCCGCCATCCTGCTCCTGCCAGC A C lnc-CLRN2-1 RNACentral:URS00008B79B6 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr4:17511919..17512040;chr4:17501783..17512203 26863410,26863196 MeRIP-seq:(Medium) rs940829956 Functional Loss SNV dbSNP153 33..33 33 - - - 74201 RMVar_ID_74201 Human_SNP_ID_175176096 m1A Human chr4 + 17512037 17512037 17512037 CCGTACACCAGCACCCGGCGCGCCTCGCCTGCAGCCGCCGCCGCCGCCATCCTGCTCCTGCCAGC CCGTACACCAGCACCCGGCGCGCCTCGCCTGCGGCCGCCGCCGCCGCCATCCTGCTCCTGCCAGC A G lnc-CLRN2-1 RNACentral:URS00008B79B6 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr4:17511919..17512040;chr4:17501783..17512203 26863410,26863196 MeRIP-seq:(Medium) rs940829956 Functional Loss SNV dbSNP153 33..33 33 - - - 74202 RMVar_ID_74202 Human_SNP_ID_175193270 m1A Human chr4 - 17577529 17577529 17577529 CATGTCTGCGGTGGAGAGACTCCGGCTCCCGAAACGTCTCACGGCCAGACGTCGGACGACTACTC CATGTCTGCGGTGGAGAGACTCCGGCTCCCGACACGTCTCACGGCCAGACGTCGGACGACTACTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:17577480..17577586 26863196 MeRIP-seq:(Medium) rs376220774 Functional Loss SNV dbSNP153 33..33 33 - - - 74203 RMVar_ID_74203 Human_SNP_ID_175193878 m1A Human chr4 + 17579938 17579938 17579938 TGTTAGCTGGAAAGCTGAGAGAGACTTTGAACATGTAAGTGTTGCTTGTGGGCTCTAGTTCTTAA TGTTAGCTGGAAAGCTGAGAGAGACTTTGAACGTGTAAGTGTTGCTTGTGGGCTCTAGTTCTTAA A G LAP3 Ensembl:ENSG00000002549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:17579894..17579980 26863196 MeRIP-seq:(Medium) rs773867621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1207993,Human_RBP_ID_26349916 Human_Splice_Rec_548783,Human_Splice_Rec_548807,Human_Splice_Rec_548831,Human_Splice_Rec_548835,Human_Splice_Rec_548841,Human_Splice_Rec_548865 RMVar_hsa_circ_104431,RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224972,RMVar_hsa_circ_123736,RMVar_hsa_circ_224973,RMVar_hsa_circ_224974 74204 RMVar_ID_74204 Human_SNP_ID_175194598 m1A Human chr4 + 17582351 17582351 17582351 GCAAAAAGGCAGCTGGAATCGACGAACAGGAAAACTGGCATGAAGGCAAAGAAAACATCAGAGCT GCAAAAAGGCAGCTGGAATCGACGAACAGGAAGACTGGCATGAAGGCAAAGAAAACATCAGAGCT A G LAP3 Ensembl:ENSG00000002549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:17582301..17582432 26863196 MeRIP-seq:(Medium) rs1306852820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9396221,Human_RBP_ID_18195068 Human_Splice_Rec_548786,Human_Splice_Rec_548787,Human_Splice_Rec_548810,Human_Splice_Rec_548811,Human_Splice_Rec_548838,Human_Splice_Rec_548844,Human_Splice_Rec_548845 RMVar_hsa_circ_52402,RMVar_hsa_circ_120628,RMVar_hsa_circ_78532,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_123736,RMVar_hsa_circ_224973,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224975,RMVar_hsa_circ_59547,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_224977 74205 RMVar_ID_74205 Human_SNP_ID_175194599 m1A Human chr4 + 17582352 17582352 17582352 CAAAAAGGCAGCTGGAATCGACGAACAGGAAAACTGGCATGAAGGCAAAGAAAACATCAGAGCTG CAAAAAGGCAGCTGGAATCGACGAACAGGAAACCTGGCATGAAGGCAAAGAAAACATCAGAGCTG A C LAP3 Ensembl:ENSG00000002549 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:17582301..17582400 26863196 MeRIP-seq:(Medium) rs200442975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9396221,Human_RBP_ID_18195068 Human_Splice_Rec_548786,Human_Splice_Rec_548787,Human_Splice_Rec_548810,Human_Splice_Rec_548811,Human_Splice_Rec_548838,Human_Splice_Rec_548844,Human_Splice_Rec_548845 RMVar_hsa_circ_52402,RMVar_hsa_circ_120628,RMVar_hsa_circ_78532,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_123736,RMVar_hsa_circ_224973,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224975,RMVar_hsa_circ_59547,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_224977 74206 RMVar_ID_74206 Human_SNP_ID_175194600 m1A Human chr4 + 17582352 17582352 17582352 CAAAAAGGCAGCTGGAATCGACGAACAGGAAAACTGGCATGAAGGCAAAGAAAACATCAGAGCTG CAAAAAGGCAGCTGGAATCGACGAACAGGAAAGCTGGCATGAAGGCAAAGAAAACATCAGAGCTG A G LAP3 Ensembl:ENSG00000002549 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:17582301..17582400 26863196 MeRIP-seq:(Medium) rs200442975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9396221,Human_RBP_ID_18195068 Human_Splice_Rec_548786,Human_Splice_Rec_548787,Human_Splice_Rec_548810,Human_Splice_Rec_548811,Human_Splice_Rec_548838,Human_Splice_Rec_548844,Human_Splice_Rec_548845 RMVar_hsa_circ_52402,RMVar_hsa_circ_120628,RMVar_hsa_circ_78532,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_123736,RMVar_hsa_circ_224973,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224975,RMVar_hsa_circ_59547,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_224977 74207 RMVar_ID_74207 Human_SNP_ID_175194894 m1A Human chr4 - 17583522 17583522 17583522 CAGCCTGAGCGTCTCCACAGGGATCCACCTCCACAGACGAGAGCTCCAGGTCTTGAATCTGCCTG CAGCCTGAGCGTCTCCACAGGGATCCACCTCCGCAGACGAGAGCTCCAGGTCTTGAATCTGCCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:17583476..17583625 26863196 MeRIP-seq:(Medium) rs1206158607 Functional Loss SNV dbSNP153 33..33 33 - - - 74208 RMVar_ID_74208 Human_SNP_ID_175194899 m1A Human chr4 + 17583541 17583541 17583541 GAGCTCTCGTCTGTGGAGGTGGATCCCTGTGGAGACGCTCAGGCTGCTGCGGAGGGAGCGGTGCT GAGCTCTCGTCTGTGGAGGTGGATCCCTGTGGCGACGCTCAGGCTGCTGCGGAGGGAGCGGTGCT A C LAP3 Ensembl:ENSG00000002549 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:17583439..17583561 26863196 MeRIP-seq:(Medium) rs896536130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785588,Human_RBP_ID_8881954,Human_RBP_ID_9304143,Human_RBP_ID_9396223,Human_RBP_ID_19013657,Human_RBP_ID_19121550,Human_RBP_ID_22457850,Human_RBP_ID_24384774,Human_RBP_ID_26349918,Human_RBP_ID_27824005 Human_Splice_Rec_548788,Human_Splice_Rec_548812,Human_Splice_Rec_548846,Human_Splice_Rec_548868,Human_Splice_Rec_548872 RMVar_hsa_circ_52402,RMVar_hsa_circ_120628,RMVar_hsa_circ_78532,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_123736,RMVar_hsa_circ_224973,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224975,RMVar_hsa_circ_59547,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_224978 74209 RMVar_ID_74209 Human_SNP_ID_175203198 m1A Human chr4 - 17614735 17614735 17614735 CTAGGAGCGCCTGGAGCTGCCTGAAGAAGCGAAGCTTGGCCCGGAAGGCCCGGCGGGGCCTGAGG CTAGGAGCGCCTGGAGCTGCCTGAAGAAGCGATGCTTGGCCCGGAAGGCCCGGCGGGGCCTGAGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:17614685..17614759 26863196 MeRIP-seq:(Medium) rs1221166465 Functional Loss SNV dbSNP153 33..33 33 - - - 74210 RMVar_ID_74210 Human_SNP_ID_175206068 m1A Human chr4 + 17623734 17623734 17623734 CGTGCAGCACAAAAAGCCCGCCGACATCCCTCAGGGCTCCTTGGCCTACCTGGAGCAGGCATCTG CGTGCAGCACAAAAAGCCCGCCGACATCCCTCGGGGCTCCTTGGCCTACCTGGAGCAGGCATCTG A G MED28 Ensembl:ENSG00000118579 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:17623683..17623773 26863196 MeRIP-seq:(Medium) rs879154007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_616974,Human_RBP_ID_787040,Human_RBP_ID_9153084,Human_RBP_ID_15098557,Human_RBP_ID_22458156,Human_RBP_ID_23034792 Human_Splice_Rec_548939 RMVar_hsa_circ_275655,RMVar_hsa_circ_298523 74211 RMVar_ID_74211 Human_SNP_ID_175251796 m1A Human chr4 - 17801225 17801225 17801225 ACTTGGGAGGCTAAGACAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT ACTTGGGAGGCTAAGACAGGAGAATTGCTTGACCCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT T G DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs761391935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22609726,Human_RBP_ID_26791567 RMVar_hsa_circ_94445,RMVar_hsa_circ_127029,RMVar_hsa_circ_224990,RMVar_hsa_circ_104206,RMVar_hsa_circ_224991,RMVar_hsa_circ_224992,RMVar_hsa_circ_224993 74212 RMVar_ID_74212 Human_SNP_ID_175252460 m1A Human chr4 - 17803668 17803668 17803668 GCCACCAAACAGCTAAGCCGAACATTGAGTAGAGCCACTCCCATACCTGAATACCTAAAACAGAT GCCACCAAACAGCTAAGCCGAACATTGAGTAGGGCCACTCCCATACCTGAATACCTAAAACAGAT T C DCAF16 Ensembl:ENSG00000163257 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:17803617..17803805 26863196 MeRIP-seq:(Medium) rs766075016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786151,Human_RBP_ID_15101357,Human_RBP_ID_27507241 RMVar_hsa_circ_94445,RMVar_hsa_circ_127029,RMVar_hsa_circ_224990,RMVar_hsa_circ_104206,RMVar_hsa_circ_224991,RMVar_hsa_circ_224992,RMVar_hsa_circ_224993 74213 RMVar_ID_74213 Human_SNP_ID_175252461 m1A Human chr4 - 17803668 17803668 17803668 GCCACCAAACAGCTAAGCCGAACATTGAGTAGAGCCACTCCCATACCTGAATACCTAAAACAGAT GCCACCAAACAGCTAAGCCGAACATTGAGTAGCGCCACTCCCATACCTGAATACCTAAAACAGAT T G DCAF16 Ensembl:ENSG00000163257 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:17803617..17803805 26863196 MeRIP-seq:(Medium) rs766075016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786151,Human_RBP_ID_15101357,Human_RBP_ID_27507241 RMVar_hsa_circ_94445,RMVar_hsa_circ_127029,RMVar_hsa_circ_224990,RMVar_hsa_circ_104206,RMVar_hsa_circ_224991,RMVar_hsa_circ_224992,RMVar_hsa_circ_224993 74214 RMVar_ID_74214 Human_SNP_ID_175254166 m1A Human chr4 + 17810661 17810661 17810661 CTCTTGGAGGATCGCTTTTTCTTTCTAGCCTCACGCTCAGCCGCACGACCCAGCCAGGCCTAACG CTCTTGGAGGATCGCTTTTTCTTTCTAGCCTCGCGCTCAGCCGCACGACCCAGCCAGGCCTAACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:17810450..17810726 26863196 MeRIP-seq:(Medium) rs370596167 Functional Loss SNV dbSNP153 33..33 33 - - - 74215 RMVar_ID_74215 Human_SNP_ID_175254329 m1A Human chr4 + 17811028 17811028 17811028 GGAGAGCGCTGCCTCTGGGTTGGCGGGCTGGCAGGCTGTAGCCGAGCGCGGGCAGGACTCGTCCC GGAGAGCGCTGCCTCTGGGTTGGCGGGCTGGCGGGCTGTAGCCGAGCGCGGGCAGGACTCGTCCC A G NCAPG Ensembl:ENSG00000109805 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:17810976..17811200 26863196 MeRIP-seq:(Medium) rs1261169133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617414,Human_RBP_ID_4794892,Human_RBP_ID_5150959,Human_RBP_ID_8943748,Human_RBP_ID_9304144,Human_RBP_ID_9334652,Human_RBP_ID_18424558,Human_RBP_ID_19014374,Human_RBP_ID_22095456,Human_RBP_ID_24046390 RMVar_hsa_circ_127133,RMVar_hsa_circ_224998,RMVar_hsa_circ_116742,RMVar_hsa_circ_224997 74216 RMVar_ID_74216 Human_SNP_ID_175254332 m1A Human chr4 - 17811032 17811032 17811032 TGCCGGGACGAGTCCTGCCCGCGCTCGGCTACAGCCTGCCAGCCCGCCAACCCAGAGGCAGCGCT TGCCGGGACGAGTCCTGCCCGCGCTCGGCTACGGCCTGCCAGCCCGCCAACCCAGAGGCAGCGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:17810976..17811200 26863196 MeRIP-seq:(Medium) rs936469562 Functional Loss SNV dbSNP153 33..33 33 - - - 74217 RMVar_ID_74217 Human_SNP_ID_175254333 m1A Human chr4 + 17811035 17811035 17811035 GCTGCCTCTGGGTTGGCGGGCTGGCAGGCTGTAGCCGAGCGCGGGCAGGACTCGTCCCGGCAGGG GCTGCCTCTGGGTTGGCGGGCTGGCAGGCTGTGGCCGAGCGCGGGCAGGACTCGTCCCGGCAGGG A G NCAPG Ensembl:ENSG00000109805 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:17810976..17811200 26863196 MeRIP-seq:(Medium) rs1275082610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617414,Human_RBP_ID_4794892,Human_RBP_ID_8943748,Human_RBP_ID_9304144,Human_RBP_ID_9334652,Human_RBP_ID_18424558,Human_RBP_ID_19014374,Human_RBP_ID_22095456,Human_RBP_ID_24046390 RMVar_hsa_circ_127133,RMVar_hsa_circ_224998,RMVar_hsa_circ_116742,RMVar_hsa_circ_224997 74218 RMVar_ID_74218 Human_SNP_ID_175268115 m1A Human chr4 + 17869521 17869521 17869521 CATTGCCTTCTCCCTTCTTACAACACATTTCCATTCACCACATTCTCCAGGCTTTCCTCTTACCT CATTGCCTTCTCCCTTCTTACAACACATTTCCGTTCACCACATTCTCCAGGCTTTCCTCTTACCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:17869497..17869587 26863196 MeRIP-seq:(Medium) rs571660531 Functional Loss SNV dbSNP153 33..33 33 - - - 74219 RMVar_ID_74219 Human_SNP_ID_175278212 m1A Human chr4 + 17912645 17912645 17912645 GGAGATGGACCTGGACTTGATGAGAAATCTGGAGGCCAGCTTGGAGAATGGCCTGAGGGAGGTGG GGAGATGGACCTGGACTTGATGAGAAATCTGGTGGCCAGCTTGGAGAATGGCCTGAGGGAGGTGG A T KRT18P63 Ensembl:ENSG00000235413 Pseudogene intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:17912638..17912750 32194978 MeRIP-seq:(Medium) rs1361957720 Functional Loss SNV dbSNP153 33..33 33 - - - 74220 RMVar_ID_74220 Human_SNP_ID_175302101 m1A Human chr4 - 18009230 18009230 18009230 AGCCAGGCTTCTCATTGTCTGAGAAGGGATTTACTAATATGAAAGTAGGGAAAATTAGAATGCTG AGCCAGGCTTCTCATTGTCTGAGAAGGGATTTGCTAATATGAAAGTAGGGAAAATTAGAATGCTG T C LCORL Ensembl:ENSG00000178177 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:18009228..18009586 26863196 MeRIP-seq:(Medium) rs931539214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225024 74221 RMVar_ID_74221 Human_SNP_ID_175302110 m1A Human chr4 + 18009266 18009266 18009266 TCCCTTCTCAGACAATGAGAAGCCTGGCTCCCATTATTCTTAATACTGATCAATCTTCATGTACG TCCCTTCTCAGACAATGAGAAGCCTGGCTCCCGTTATTCTTAATACTGATCAATCTTCATGTACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18009264..18009600 26863196 MeRIP-seq:(Medium) rs888323861 Functional Loss SNV dbSNP153 33..33 33 - - - 74222 RMVar_ID_74222 Human_SNP_ID_175305324 m1A Human chr4 + 18021710 18021689 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCG_____________________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs758596593 Functional Loss DEL dbSNP153 13..33 33 - - - 74223 RMVar_ID_74223 Human_SNP_ID_175305328 m1A Human chr4 + 18021722 18021692 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCG______________________________GCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GGCGGCGGCGGCGGCAGCAGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs777784124 Functional Loss DEL dbSNP153 4..33 33 - - - 74224 RMVar_ID_74224 Human_SNP_ID_175305331 m1A Human chr4 + 18021707 18021692 18021707 CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT CTCCGGCACTGAGCGGCG_______________GCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT GGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18021625..18021734 26863196 MeRIP-seq:(Medium) rs1256001696 Functional Loss DEL dbSNP153 19..33 33 - - - 74225 RMVar_ID_74225 Human_SNP_ID_175305333 m1A Human chr4 + 18021710 18021692 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCG__________________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs1553889932 Functional Loss DEL dbSNP153 16..33 33 - - - 74226 RMVar_ID_74226 Human_SNP_ID_175305337 m1A Human chr4 + 18021722 18021695 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCG___________________________GCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GGCGGCGGCGGCAGCAGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs778684593 Functional Loss DEL dbSNP153 7..33 33 - - - 74227 RMVar_ID_74227 Human_SNP_ID_175305340 m1A Human chr4 + 18021710 18021695 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCGGCG_______________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs748702669 Functional Loss DEL dbSNP153 19..33 33 - - - 74228 RMVar_ID_74228 Human_SNP_ID_175305342 m1A Human chr4 + 18021707 18021695 18021707 CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT CTCCGGCACTGAGCGGCGGCG____________GCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT GGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18021625..18021734 26863196 MeRIP-seq:(Medium) rs756828467 Functional Loss DEL dbSNP153 22..33 33 - - - 74229 RMVar_ID_74229 Human_SNP_ID_175305345 m1A Human chr4 + 18021722 18021698 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCGGCG________________________GCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GGCGGCGGCAGCAGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs745576661 Functional Loss DEL dbSNP153 10..33 33 - - - 74230 RMVar_ID_74230 Human_SNP_ID_175305347 m1A Human chr4 + 18021710 18021698 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCGGCGGCG____________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs769142181 Functional Loss DEL dbSNP153 22..33 33 - - - 74231 RMVar_ID_74231 Human_SNP_ID_175305349 m1A Human chr4 + 18021707 18021698 18021707 CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT CTCCGGCACTGAGCGGCGGCGGCG_________GCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT GGCGGCGGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18021625..18021734 26863196 MeRIP-seq:(Medium) rs1456468352 Functional Loss DEL dbSNP153 25..33 33 - - - 74232 RMVar_ID_74232 Human_SNP_ID_175305352 m1A Human chr4 + 18021722 18021701 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCGGCGGCG_____________________GCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GGCGGCAGCAGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs777073080 Functional Loss DEL dbSNP153 13..33 33 - - - 74233 RMVar_ID_74233 Human_SNP_ID_175305355 m1A Human chr4 + 18021710 18021701 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCGGCGGCGGCG_________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs1355428409 Functional Loss DEL dbSNP153 25..33 33 - - - 74234 RMVar_ID_74234 Human_SNP_ID_175305363 m1A Human chr4 + 18021707 18021707 18021707 CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18021625..18021734 26863196 MeRIP-seq:(Medium) rs748344642 Functional Loss SNV dbSNP153 33..33 33 - - - 74235 RMVar_ID_74235 Human_SNP_ID_175305370 m1A Human chr4 + 18021710 18021710 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs942593850 Functional Loss SNV dbSNP153 33..33 33 - - - 74236 RMVar_ID_74236 Human_SNP_ID_175305391 m1A Human chr4 + 18021722 18021722 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs777252972 Functional Loss SNV dbSNP153 33..33 33 - - - 74237 RMVar_ID_74237 Human_SNP_ID_175305392 m1A Human chr4 + 18021722 18021722 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCTGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs777252972 Functional Loss SNV dbSNP153 33..33 33 - - - 74238 RMVar_ID_74238 Human_SNP_ID_175862456 m1A Human chr4 + 20252020 20252020 20252020 AAAAAAGAAGGCGGCGGCGGCGGCGGCGGCGGAGGCGGAGGCAGCTGCGAGGCATGGGAGCGCCG AAAAAAGAAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCAGCTGCGAGGCATGGGAGCGCCG A C SLIT2 Ensembl:ENSG00000145147 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:20251901..20252168 26863196 MeRIP-seq:(Medium) rs532053983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4781240,Human_RBP_ID_5475411,Human_RBP_ID_22094096,Human_RBP_ID_27065094 74239 RMVar_ID_74239 Human_SNP_ID_175862457 m1A Human chr4 + 20252020 20252020 20252020 AAAAAAGAAGGCGGCGGCGGCGGCGGCGGCGGAGGCGGAGGCAGCTGCGAGGCATGGGAGCGCCG AAAAAAGAAGGCGGCGGCGGCGGCGGCGGCGGGGGCGGAGGCAGCTGCGAGGCATGGGAGCGCCG A G SLIT2 Ensembl:ENSG00000145147 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:20251901..20252168 26863196 MeRIP-seq:(Medium) rs532053983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4781240,Human_RBP_ID_5475411,Human_RBP_ID_22094096,Human_RBP_ID_27065094 74240 RMVar_ID_74240 Human_SNP_ID_175862497 m1A Human chr4 + 20252121 20252121 20252121 TGGGCACGGCGGGAGTGCTGAGCAGAAAGGGGAGCGCCGGGGGCCCGCAGCCGGCTCCGGAGGCG TGGGCACGGCGGGAGTGCTGAGCAGAAAGGGGGGCGCCGGGGGCCCGCAGCCGGCTCCGGAGGCG A G SLIT2 Ensembl:ENSG00000145147 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:20252083..20252188 32194978 MeRIP-seq:(Medium) rs1012791764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27065097 74241 RMVar_ID_74241 Human_SNP_ID_175978957 m1A Human chr4 - 20704619 20704619 20704619 AAACAGAACATCAATAGAAACCAGGTACAAGCAATAAAGTTCACCCTGCATCCATCTGTAGCACA AAACAGAACATCAATAGAAACCAGGTACAAGCTATAAAGTTCACCCTGCATCCATCTGTAGCACA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:20704618..20704718 26863196 MeRIP-seq:(Medium) rs1291013971 Functional Loss SNV dbSNP153 33..33 33 - - - 74242 RMVar_ID_74242 Human_SNP_ID_176446373 m1A Human chr4 - 22510654 22510654 22510654 CGGGAGGAAGGGTGGCAGGTGGTGGCTGGCCCACTTGAAGTGGAGAGACGGTATCGGACGAATAG CGGGAGGAAGGGTGGCAGGTGGTGGCTGGCCCGCTTGAAGTGGAGAGACGGTATCGGACGAATAG T C ADGRA3 Ensembl:ENSG00000152990 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:22510528..22510699 26863196 MeRIP-seq:(Medium) rs996105983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24051010 74243 RMVar_ID_74243 Human_SNP_ID_176447793 m1A Human chr4 - 22515625 22515625 22515625 GCAAGCACGATGGGCGGCCCCGAGGGGCTGGCAGGGCGGCGGGCGCCGCCGAGGGCAAGGTGGTG GCAAGCACGATGGGCGGCCCCGAGGGGCTGGCGGGGCGGCGGGCGCCGCCGAGGGCAAGGTGGTG T C ADGRA3 Ensembl:ENSG00000152990 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:22515574..22515682 26863196 MeRIP-seq:(Medium) rs1230522457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795354 Human_Splice_Rec_550113,Human_Splice_Rec_550203,Human_Splice_Rec_550265 74244 RMVar_ID_74244 Human_SNP_ID_176447898 m1A Human chr4 - 22515801 22515801 22515801 CCGCTAGGCCAGTGCGCCGCCGCTCGCCCCGCAGGCCCCGGCCCGCAGCATGGAGCCACCCGGAC CCGCTAGGCCAGTGCGCCGCCGCTCGCCCCGCTGGCCCCGGCCCGCAGCATGGAGCCACCCGGAC T A ADGRA3 Ensembl:ENSG00000152990 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:22515751..22516078 26863196 MeRIP-seq:(Medium) rs898236662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794581,Human_RBP_ID_5242155 74245 RMVar_ID_74245 Human_SNP_ID_176447948 m1A Human chr4 + 22515908 22515908 22515908 AGCGGCGACCGGAGCCTTATGGCGGCCGGAGGACGGGCCTTCCCCGGCGCGGACATGCTCCTTTG AGCGGCGACCGGAGCCTTATGGCGGCCGGAGGGCGGGCCTTCCCCGGCGCGGACATGCTCCTTTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:22515841..22516016 26863196 MeRIP-seq:(Medium) rs977504120 Functional Loss SNV dbSNP153 33..33 33 - - - 74246 RMVar_ID_74246 Human_SNP_ID_176892749 m1A Human chr4 - 24292465 24292465 24292465 AGGGGTTAGGAAGGAGTGCACATAGGGGAGGCAGAAAGGCAGGCATGAGGGAAACCTTCCTGATG AGGGGTTAGGAAGGAGTGCACATAGGGGAGGCCGAAAGGCAGGCATGAGGGAAACCTTCCTGATG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:24292295..24292495 26863196 MeRIP-seq:(Medium) rs1414594488 Functional Loss SNV dbSNP153 33..33 33 - - - 74247 RMVar_ID_74247 Human_SNP_ID_176893321 m1A Human chr4 - 24293466 24293466 24293466 AGTGGTGAGAGGTGAGGGGGTAGGAGGAGTGCAGGCAGGGGTGAGAGGTGAGGGGGTAGGAGGAG AGTGGTGAGAGGTGAGGGGGTAGGAGGAGTGCCGGCAGGGGTGAGAGGTGAGGGGGTAGGAGGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24293417..24293542 26863196 MeRIP-seq:(Medium) rs1306542395 Functional Loss SNV dbSNP153 33..33 33 - - - 74248 RMVar_ID_74248 Human_SNP_ID_176893346 m1A Human chr4 - 24293531 24293531 24293531 AGGGGTAAGGGGGTAGGAGGAGCACAGGCAGCAGTGGGGCTGAGGGGGTAGGGAGGAGTGCAGGC AGGGGTAAGGGGGTAGGAGGAGCACAGGCAGCGGTGGGGCTGAGGGGGTAGGGAGGAGTGCAGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:24293397..24293572 26863196 MeRIP-seq:(Medium) rs1346324145 Functional Loss SNV dbSNP153 33..33 33 - - - 74249 RMVar_ID_74249 Human_SNP_ID_176901276 m1A Human chr4 - 24324910 24324910 24324910 GAGGAGCGGAGGCTGAGGAATTATTGGGACCTAGCTTGGGCTGGCGAGGAGGGGAGAGGTCAGAT GAGGAGCGGAGGCTGAGGAATTATTGGGACCTGGCTTGGGCTGGCGAGGAGGGGAGAGGTCAGAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24324859..24325020 26863196 MeRIP-seq:(Medium) rs1387974332 Functional Loss SNV dbSNP153 33..33 33 - - - 74250 RMVar_ID_74250 Human_SNP_ID_176901537 m1A Human chr4 + 24325718 24325718 24325718 CCGATCGCCTCGGAAGCCCCGTAGACCACCACAGATGCCGAGCTTTGAGTAACTCTCACAGTGGA CCGATCGCCTCGGAAGCCCCGTAGACCACCACGGATGCCGAGCTTTGAGTAACTCTCACAGTGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:24325620..24325724 26863196 MeRIP-seq:(Medium) rs538183543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2843053 74251 RMVar_ID_74251 Human_SNP_ID_176901992 m1A Human chr4 + 24327277 24327277 24327277 TAGACTGTGCCCCCAAATAATTTGTCATCCCTACTATCTTCTGTCTAGTCATACTCCTATTCACT TAGACTGTGCCCCCAAATAATTTGTCATCCCTGCTATCTTCTGTCTAGTCATACTCCTATTCACT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:24327226..24327300 26863196 MeRIP-seq:(Medium) rs1464146746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20976960 74252 RMVar_ID_74252 Human_SNP_ID_176902085 m1A Human chr4 - 24327633 24327633 24327633 CAGATTAAGCTGAAGGGAGATCTTGTGGTAAGAGGTGATATTGTGGGGTTGTTAGAAGAAACATT CAGATTAAGCTGAAGGGAGATCTTGTGGTAAGGGGTGATATTGTGGGGTTGTTAGAAGAAACATT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:24327583..24327721;chr4:24327582..24327775 26863196 MeRIP-seq:(Medium) rs562171668 Functional Loss SNV dbSNP153 33..33 33 - - - 74253 RMVar_ID_74253 Human_SNP_ID_176902089 m1A Human chr4 + 24327643 24327643 24327643 CTAACAACCCCACAATATCACCTCTTACCACAAGATCTCCCTTCAGCTTAATCTGTCCCACTCTA CTAACAACCCCACAATATCACCTCTTACCACACGATCTCCCTTCAGCTTAATCTGTCCCACTCTA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:24327595..24327710 26863196 MeRIP-seq:(Medium) rs1214404700 Functional Loss SNV dbSNP153 33..33 33 - - - 74254 RMVar_ID_74254 Human_SNP_ID_176902090 m1A Human chr4 - 24327646 24327646 24327646 ACGTAGAGTGGGACAGATTAAGCTGAAGGGAGATCTTGTGGTAAGAGGTGATATTGTGGGGTTGT ACGTAGAGTGGGACAGATTAAGCTGAAGGGAGGTCTTGTGGTAAGAGGTGATATTGTGGGGTTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:24327596..24327726 26863196 MeRIP-seq:(Medium) rs6815036 Functional Loss SNV dbSNP153 33..33 33 - - - 74255 RMVar_ID_74255 Human_SNP_ID_176902607 m1A Human chr4 - 24329400 24329400 24329400 CAGTGGCAGGAGCCGGAGCTGGAGAGGCAGGTAGGACCCCATCACGCAGGGCCTCAAAGGCTTGT CAGTGGCAGGAGCCGGAGCTGGAGAGGCAGGTTGGACCCCATCACGCAGGGCCTCAAAGGCTTGT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:24329351..24329400 26863196 MeRIP-seq:(Medium) rs988839966 Functional Loss SNV dbSNP153 33..33 33 - - - 74256 RMVar_ID_74256 Human_SNP_ID_176902608 m1A Human chr4 - 24329400 24329400 24329400 CAGTGGCAGGAGCCGGAGCTGGAGAGGCAGGTAGGACCCCATCACGCAGGGCCTCAAAGGCTTGT CAGTGGCAGGAGCCGGAGCTGGAGAGGCAGGTGGGACCCCATCACGCAGGGCCTCAAAGGCTTGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:24329351..24329400 26863196 MeRIP-seq:(Medium) rs988839966 Functional Loss SNV dbSNP153 33..33 33 - - - 74257 RMVar_ID_74257 Human_SNP_ID_176910400 m1A Human chr4 + 24361110 24361108 24361111 AGGTGACCACTTGCTCCAGTGTGGCTGGGACAAGAAGGAACTGCGGCAACAGCAGAGGGGCAGGG AGGTGACCACTTGCTCCAGTGTGGCTGGGAC___AAGGAACTGCGGCAACAGCAGAGGGGCAGGG CAAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24361059..24361246 26863196 MeRIP-seq:(Medium) rs777308549 Functional Loss DEL dbSNP153 32..34 33 - - - 74258 RMVar_ID_74258 Human_SNP_ID_176910402 m1A Human chr4 + 24361116 24361116 24361116 CCACTTGCTCCAGTGTGGCTGGGACAAGAAGGAACTGCGGCAACAGCAGAGGGGCAGGGACAAGA CCACTTGCTCCAGTGTGGCTGGGACAAGAAGGGACTGCGGCAACAGCAGAGGGGCAGGGACAAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:24361066..24361175 26863196 MeRIP-seq:(Medium) rs753857864 Functional Loss SNV dbSNP153 33..33 33 - - - 74259 RMVar_ID_74259 Human_SNP_ID_176910413 m1A Human chr4 + 24361153 24361150 24361153 CGGCAACAGCAGAGGGGCAGGGACAAGAAGGAAGAAGGAGCCAGCAGAGGACAGGGAAGGAGTCA CGGCAACAGCAGAGGGGCAGGGACAAGAAG___GAAGGAGCCAGCAGAGGACAGGGAAGGAGTCA GGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:24361051..24361219 26863196 MeRIP-seq:(Medium) rs1183462352 Functional Loss DEL dbSNP153 31..33 33 - - - 74260 RMVar_ID_74260 Human_SNP_ID_176916560 m1A Human chr4 + 24387734 24387734 24387734 ACTCCAGCCTGGCAAAAGAGTGAGATTCCATCAAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAG ACTCCAGCCTGGCAAAAGAGTGAGATTCCATCGAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24387688..24387762 26863196 MeRIP-seq:(Medium) rs1303981292 Functional Loss SNV dbSNP153 33..33 33 - - - 74261 RMVar_ID_74261 Human_SNP_ID_176917114 m1A Human chr4 + 24388053 24388053 24388053 AAGAAAGAAACTATCATCAGAGTGAACAGGCAAATTACAGAATGGAAGAAAATTTTTGCAATCTA AAGAAAGAAACTATCATCAGAGTGAACAGGCAGATTACAGAATGGAAGAAAATTTTTGCAATCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24388002..24388067 26863196 MeRIP-seq:(Medium) rs1435123702 Functional Loss SNV dbSNP153 33..33 33 - - - 74262 RMVar_ID_74262 Human_SNP_ID_176937073 m1A Human chr4 + 24471330 24471327 24471331 AGACACGCGAGCGCGCGCGCACACCCACACACAGACACACACCCGCGTGCACACACACACACACG AGACACGCGAGCGCGCGCGCACACCCACAC____ACACACACCCGCGTGCACACACACACACACG CACAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24471300..24471401 26863196 MeRIP-seq:(Medium) rs1197200638 Functional Loss DEL dbSNP153 31..34 33 - - - 74263 RMVar_ID_74263 Human_SNP_ID_176937319 m1A Human chr4 + 24472063 24472063 24472063 AGGTTGCGCTCGAGTTCCCTGGTTCTGCCTGGAGTTGTTCGGGGTAACGCGCCGGCTCCTGCCTC AGGTTGCGCTCGAGTTCCCTGGTTCTGCCTGGGGTTGTTCGGGGTAACGCGCCGGCTCCTGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24472055..24472131 26863196 MeRIP-seq:(Medium) rs985684939 Functional Loss SNV dbSNP153 33..33 33 - - - 74264 RMVar_ID_74264 Human_SNP_ID_176937573 m1A Human chr4 - 24472789 24472789 24472789 TCGCTCTGCGCGCACACACCACACACACGCACACGCACACACACGCGCGCACACACGCAGCCGGC TCGCTCTGCGCGCACACACCACACACACGCACGCGCACACACACGCGCGCACACACGCAGCCGGC T C lnc-DHX15-1,lnc-DHX15-1:2 RNACentral:URS0000D5A8EE,RNACentral:URS00008B6996 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:24472763..24472878 26863196 MeRIP-seq:(Medium) rs555911388 Functional Loss SNV dbSNP153 33..33 33 - - - 74265 RMVar_ID_74265 Human_SNP_ID_176951171 m1A Human chr4 + 24522821 24522821 24522821 TTTTCTAAATGACTTCAGTGAACCCTCTTCCGACAATCTATCCTCTATATTGAACTCAGATGCAC TTTTCTAAATGACTTCAGTGAACCCTCTTCCGTCAATCTATCCTCTATATTGAACTCAGATGCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:24522770..24522938 26863196 MeRIP-seq:(Medium) rs1434785108 Functional Loss SNV dbSNP153 33..33 33 - - - 74266 RMVar_ID_74266 Human_SNP_ID_176963690 m1A Human chr4 - 24570668 24570668 24570668 TACTCCATTCGATTTGAAGACTGCAGTAGTGCAAAAACCATTCTTAAGTAAGTACTATATCTTTA TACTCCATTCGATTTGAAGACTGCAGTAGTGCGAAAACCATTCTTAAGTAAGTACTATATCTTTA T C DHX15 Ensembl:ENSG00000109606 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:24556351..24576283 32194978 MeRIP-seq:(Medium) rs1450958245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1036251,Human_RBP_ID_1977417,Human_RBP_ID_3737093,Human_RBP_ID_3966654,Human_RBP_ID_5475914,Human_RBP_ID_5610108,Human_RBP_ID_15129413,Human_RBP_ID_22510593,Human_RBP_ID_24051306,Human_RBP_ID_27727071 Human_Splice_Rec_550813 Human_miRNA_ID_2004464 RMVar_hsa_circ_7805,RMVar_hsa_circ_65157,RMVar_hsa_circ_73969,RMVar_hsa_circ_28349,RMVar_hsa_circ_21820,RMVar_hsa_circ_67721,RMVar_hsa_circ_318498,RMVar_hsa_circ_342014,RMVar_hsa_circ_319933,RMVar_hsa_circ_355792,RMVar_hsa_circ_98823,RMVar_hsa_circ_225125,RMVar_hsa_circ_281510,RMVar_hsa_circ_225126 74267 RMVar_ID_74267 Human_SNP_ID_176967283 m1A Human chr4 + 24583623 24583623 24583623 TAGTATCTACTTTGAAGTGTTTGAATGGACCAAGGCACGCTCTCTCCCGCCAAACTATAAACTCA TAGTATCTACTTTGAAGTGTTTGAATGGACCACGGCACGCTCTCTCCCGCCAAACTATAAACTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24583621..24583860 26863196 MeRIP-seq:(Medium) rs1280089170 Functional Loss SNV dbSNP153 33..33 33 - - - 74268 RMVar_ID_74268 Human_SNP_ID_176967614 m1A Human chr4 - 24584475 24584475 24584475 GGCTGTAGTAGCGGGAGGGGTGGGGGTCCTCCAGAGTTAAGTGGCTGTCCTCGACTGTGCCCATA GGCTGTAGTAGCGGGAGGGGTGGGGGTCCTCCGGAGTTAAGTGGCTGTCCTCGACTGTGCCCATA T C DHX15 Ensembl:ENSG00000109606 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:24584168..24584550;chr4:24584006..24584550 26863196 MeRIP-seq:(Medium) rs1269288128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72550,Human_RBP_ID_1036259,Human_RBP_ID_3966657,Human_RBP_ID_4799023,Human_RBP_ID_5531229,Human_RBP_ID_7301267,Human_RBP_ID_15129758,Human_RBP_ID_22609766,Human_RBP_ID_22826037,Human_RBP_ID_26348882 74269 RMVar_ID_74269 Human_SNP_ID_177047579 m1A Human chr4 + 24912824 24912824 24912824 CGCCTGGCCGGCGCCGCGGCCTCACCTCGCTCACCAGCCCCTGCCAGTCGCTCTCAGTCCGGTCG CGCCTGGCCGGCGCCGCGGCCTCACCTCGCTCCCCAGCCCCTGCCAGTCGCTCTCAGTCCGGTCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:24912812..24913010 26863196 MeRIP-seq:(Medium) rs978717419 Functional Loss SNV dbSNP153 33..33 33 - - - 74270 RMVar_ID_74270 Human_SNP_ID_177143397 m1A Human chr4 - 25312883 25312883 25312883 GGACGGCAGGATCCAAAGGAAGCACCACCTCCATTCCCGAGCTTCCCCGGCACCCTGCGCTGCCC GGACGGCAGGATCCAAAGGAAGCACCACCTCCGTTCCCGAGCTTCCCCGGCACCCTGCGCTGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:25312833..25314094;chr4:25312834..25314094 26863196 MeRIP-seq:(Medium) rs1178304392 Functional Loss SNV dbSNP153 33..33 33 - - - 74271 RMVar_ID_74271 Human_SNP_ID_177163926 m1A Human chr4 + 25398387 25398387 25398387 AGGCCTCACTGAGAAGGTGAAGTTGGAAGGAGACGGAAGGGAGCAAGCCCTGTTGATATTTGGGG AGGCCTCACTGAGAAGGTGAAGTTGGAAGGAGGCGGAAGGGAGCAAGCCCTGTTGATATTTGGGG A G ANAPC4 Ensembl:ENSG00000053900 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:25398344..25398432 26863196 MeRIP-seq:(Medium) rs1449896365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15131719 RMVar_hsa_circ_353442,RMVar_hsa_circ_311540,RMVar_hsa_circ_8888,RMVar_hsa_circ_4631,RMVar_hsa_circ_225157,RMVar_hsa_circ_225158,RMVar_hsa_circ_47458,RMVar_hsa_circ_122017,RMVar_hsa_circ_225163,RMVar_hsa_circ_51867,RMVar_hsa_circ_10580,RMVar_hsa_circ_73489,RMVar_hsa_circ_74679,RMVar_hsa_circ_75574,RMVar_hsa_circ_6040,RMVar_hsa_circ_43000,RMVar_hsa_circ_118759,RMVar_hsa_circ_376652,RMVar_hsa_circ_225166,RMVar_hsa_circ_47868,RMVar_hsa_circ_48942,RMVar_hsa_circ_225167,RMVar_hsa_circ_40804 74272 RMVar_ID_74272 Human_SNP_ID_177164370 m1A Human chr4 + 25400316 25400316 25400316 GTGAGAGAGGTGGGACCTAGTGCAGAAGGGAAAGGGTTGGAAAAGCAGAGGTAGGAGCTCATCAG GTGAGAGAGGTGGGACCTAGTGCAGAAGGGAAGGGGTTGGAAAAGCAGAGGTAGGAGCTCATCAG A G ANAPC4 Ensembl:ENSG00000053900 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:25400239..25400910 26863196 MeRIP-seq:(Medium) rs1341670405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7301909 RMVar_hsa_circ_353442,RMVar_hsa_circ_311540,RMVar_hsa_circ_8888,RMVar_hsa_circ_4631,RMVar_hsa_circ_225157,RMVar_hsa_circ_225158,RMVar_hsa_circ_47458,RMVar_hsa_circ_122017,RMVar_hsa_circ_225163,RMVar_hsa_circ_51867,RMVar_hsa_circ_10580,RMVar_hsa_circ_73489,RMVar_hsa_circ_74679,RMVar_hsa_circ_75574,RMVar_hsa_circ_6040,RMVar_hsa_circ_43000,RMVar_hsa_circ_118759,RMVar_hsa_circ_376652,RMVar_hsa_circ_225166,RMVar_hsa_circ_47868,RMVar_hsa_circ_48942,RMVar_hsa_circ_225167,RMVar_hsa_circ_40804 74273 RMVar_ID_74273 Human_SNP_ID_177254200 m1A Human chr4 + 25747675 25747675 25747675 ATGAAACTATAAGCTAGAGGCTTACTTGCTGCATATTCCGTTGCTGCCAGTCTATTCTAACGTGT ATGAAACTATAAGCTAGAGGCTTACTTGCTGCGTATTCCGTTGCTGCCAGTCTATTCTAACGTGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:25747626..25747727 32194978 MeRIP-seq:(Medium) rs746206856 Functional Loss SNV dbSNP153 33..33 33 - - - 74274 RMVar_ID_74274 Human_SNP_ID_177282725 m1A Human chr4 - 25862832 25862831 25862832 TTCCGGCCCGGATCCGGGCGGCCTCGCCATGCAGCGGCGCGGCGCGGGGCTCGGGTGGCCGCGGC TTCCGGCCCGGATCCGGGCGGCCTCGCCATGC_GCGGCGCGGCGCGGGGCTCGGGTGGCCGCGGC CT C SEL1L3 Ensembl:ENSG00000091490 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:25862676..25862969 26863196 MeRIP-seq:(Medium) rs1208628365 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4782949 Human_miRNA_ID_2937243 RMVar_hsa_circ_117943,RMVar_hsa_circ_225208,RMVar_hsa_circ_114341,RMVar_hsa_circ_225214,RMVar_hsa_circ_105333,RMVar_hsa_circ_225218 74275 RMVar_ID_74275 Human_SNP_ID_177282726 m1A Human chr4 + 25862835 25862835 25862835 GCGGCCACCCGAGCCCCGCGCCGCGCCGCTGCATGGCGAGGCCGCCCGGATCCGGGCCGGAACAG GCGGCCACCCGAGCCCCGCGCCGCGCCGCTGCGTGGCGAGGCCGCCCGGATCCGGGCCGGAACAG A G SMIM20 Ensembl:ENSG00000250317 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:25847825..25862984;chr4:25862697..25862981 26863196 MeRIP-seq:(Medium) rs1309384902 Functional Loss SNV dbSNP153 33..33 33 - - - 74276 RMVar_ID_74276 Human_SNP_ID_177295005 m1A Human chr4 + 25914324 25914324 25914324 GGGCAGCCCGGGGCCTGACGCCATGTCCCGGAACCTGCGCACCGCGCTCATTTTCGGCGGCTTCA GGGCAGCCCGGGGCCTGACGCCATGTCCCGGAGCCTGCGCACCGCGCTCATTTTCGGCGGCTTCA A G SMIM20 Ensembl:ENSG00000250317 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:25914274..25914368 26863196 MeRIP-seq:(Medium) rs1016826101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794586,Human_RBP_ID_8879348 Human_Splice_Rec_551717,Human_Splice_Rec_551721,Human_Splice_Rec_551725 74277 RMVar_ID_74277 Human_SNP_ID_177295028 m1A Human chr4 - 25914363 25914363 25914363 GGAAGTAGATGGGATAGAAGGCGGCGCCGATCAGGGAGATGAAGCCGCCGAAAATGAGCGCGGTG GGAAGTAGATGGGATAGAAGGCGGCGCCGATCTGGGAGATGAAGCCGCCGAAAATGAGCGCGGTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:25914276..25914373 26863410 MeRIP-seq:(Medium) rs1359083368 Functional Loss SNV dbSNP153 33..33 33 - - - 74278 RMVar_ID_74278 Human_SNP_ID_177295040 m1A Human chr4 - 25914380 25914380 25914380 CAATCTCATTAGGGGCCGGAAGTAGATGGGATAGAAGGCGGCGCCGATCAGGGAGATGAAGCCGC CAATCTCATTAGGGGCCGGAAGTAGATGGGATGGAAGGCGGCGCCGATCAGGGAGATGAAGCCGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:25914235..25914415 26863196 MeRIP-seq:(Medium) rs1028283967 Functional Loss SNV dbSNP153 33..33 33 - - - 74279 RMVar_ID_74279 Human_SNP_ID_177295044 m1A Human chr4 - 25914387 25914387 25914387 ACTCCTCCAATCTCATTAGGGGCCGGAAGTAGATGGGATAGAAGGCGGCGCCGATCAGGGAGATG ACTCCTCCAATCTCATTAGGGGCCGGAAGTAGTTGGGATAGAAGGCGGCGCCGATCAGGGAGATG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:25914249..25914401 26863196 MeRIP-seq:(Medium) rs1226234999 Functional Loss SNV dbSNP153 33..33 33 - - - 74280 RMVar_ID_74280 Human_SNP_ID_177394888 m1A Human chr4 - 26320876 26320876 26320876 TCCCTTTCCCCTCGCCGCCGCCGCGAAGAGCCAGACGCCTCGCGCCGCCCGCAGAGTAGGGGATC TCCCTTTCCCCTCGCCGCCGCCGCGAAGAGCCGGACGCCTCGCGCCGCCCGCAGAGTAGGGGATC T C lnc-CCKAR-10,lnc-CCKAR-10:2,lnc-CCKAR-10:3,lnc-CCKAR-10:4 RNACentral:URS0000D5BCCC,RNACentral:URS0000D5D104,RNACentral:URS0000D58CA5,RNACentral:URS0000D572A6 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:26320826..26321103 26863196 MeRIP-seq:(Medium) rs1463599265 Functional Loss SNV dbSNP153 33..33 33 - - - 74281 RMVar_ID_74281 Human_SNP_ID_177394889 m1A Human chr4 - 26320876 26320876 26320876 TCCCTTTCCCCTCGCCGCCGCCGCGAAGAGCCAGACGCCTCGCGCCGCCCGCAGAGTAGGGGATC TCCCTTTCCCCTCGCCGCCGCCGCGAAGAGCCCGACGCCTCGCGCCGCCCGCAGAGTAGGGGATC T G lnc-CCKAR-10,lnc-CCKAR-10:2,lnc-CCKAR-10:3,lnc-CCKAR-10:4 RNACentral:URS0000D5BCCC,RNACentral:URS0000D5D104,RNACentral:URS0000D58CA5,RNACentral:URS0000D572A6 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:26320826..26321103 26863196 MeRIP-seq:(Medium) rs1463599265 Functional Loss SNV dbSNP153 33..33 33 - - - 74282 RMVar_ID_74282 Human_SNP_ID_177394967 m1A Human chr4 - 26321042 26321042 26321042 CGGCGCTCCGATTCCCTCAGACTTACCCTGTCACAACAGGCGCCATCTTCCACAAACTCTCGCCA CGGCGCTCCGATTCCCTCAGACTTACCCTGTCGCAACAGGCGCCATCTTCCACAAACTCTCGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:26320690..26321382 26863196 MeRIP-seq:(Medium) rs1560262954 Functional Loss SNV dbSNP153 33..33 33 - - - 74283 RMVar_ID_74283 Human_SNP_ID_177399857 m1A Human chr4 - 26340146 26340146 26340146 CTTTCCCTGTTTTATTTTTCTCAGTTGCATGCATCACCTTCTAACATAATGTTAATTACTTTTAA CTTTCCCTGTTTTATTTTTCTCAGTTGCATGCGTCACCTTCTAACATAATGTTAATTACTTTTAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:26340139..26340332 26863196 MeRIP-seq:(Medium) rs890161710 Functional Loss SNV dbSNP153 33..33 33 - - - 74284 RMVar_ID_74284 Human_SNP_ID_177404047 m1A Human chr4 - 26356967 26356967 26356967 CACCAGGCTCTGCTACCTCCATGCTTGTATGCACACTTCTCTATGTGGAATCCTCTTCCTTCCAA CACCAGGCTCTGCTACCTCCATGCTTGTATGCTCACTTCTCTATGTGGAATCCTCTTCCTTCCAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:26356965..26357048 26863196 MeRIP-seq:(Medium) rs1299321446 Functional Loss SNV dbSNP153 33..33 33 - - - 74285 RMVar_ID_74285 Human_SNP_ID_177461394 m1A Human chr4 + 26584187 26584187 26584187 CGGCCTGTCCCCGCGGCTTGGCGGGCTAGGGCAGGGGAAATGTTGCAGGAGGAGTCGGACCTCTC CGGCCTGTCCCCGCGGCTTGGCGGGCTAGGGCGGGGGAAATGTTGCAGGAGGAGTCGGACCTCTC A G TBC1D19 Ensembl:ENSG00000109680 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:26584138..26584248 26863196 MeRIP-seq:(Medium) rs369271987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424566 74286 RMVar_ID_74286 Human_SNP_ID_177524555 m1A Human chr4 - 26858349 26858349 26858349 AAGCTACCCTGAGGCCCTTTTCCTTGGCACTTACCCGACTCCTACAGCCAGCCTATACCTCTCAA AAGCTACCCTGAGGCCCTTTTCCTTGGCACTTCCCCGACTCCTACAGCCAGCCTATACCTCTCAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:26858306..26858498 26863196 MeRIP-seq:(Medium) rs1339973601 Functional Loss SNV dbSNP153 33..33 33 - - - 74287 RMVar_ID_74287 Human_SNP_ID_177525226 m1A Human chr4 - 26860830 26860826 26860830 CGAGACCGGGATCCGCTGCTCTGGCGCCGCCAAACACCAACCCCAGCTCCCGCGCCGCCGCCGCC CGAGACCGGGATCCGCTGCTCTGGCGCCGCCA____CCAACCCCAGCTCCCGCGCCGCCGCCGCC GTGTT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:26860794..26860923 26863196 MeRIP-seq:(Medium) rs1240475808 Functional Loss DEL dbSNP153 33..36 33 - - - 74288 RMVar_ID_74288 Human_SNP_ID_330202041 m1A Human chr7 + 90346771 90346771 90346771 GCCATGGTGCATTGCAGTTGCGTGTTGTTCAGAAAGGTCCGTGCGGGTCCCCTCAGCCTGGTCCC GCCATGGTGCATTGCAGTTGCGTGTTGTTCAGGAAGGTCCGTGCGGGTCCCCTCAGCCTGGTCCC A G GTPBP10 Ensembl:ENSG00000105793 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:90346754..90346828;chr7:90346750..90346832;chr7:90346748..90346866 26863196 MeRIP-seq:(Medium) rs778015705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956463,Human_RBP_ID_18426042,Human_RBP_ID_19136716 Human_Splice_Rec_886815,Human_Splice_Rec_886829,Human_Splice_Rec_886843,Human_Splice_Rec_886845,Human_Splice_Rec_886861,Human_Splice_Rec_886879 74289 RMVar_ID_74289 Human_SNP_ID_330202042 m1A Human chr7 + 90346771 90346771 90346771 GCCATGGTGCATTGCAGTTGCGTGTTGTTCAGAAAGGTCCGTGCGGGTCCCCTCAGCCTGGTCCC GCCATGGTGCATTGCAGTTGCGTGTTGTTCAGTAAGGTCCGTGCGGGTCCCCTCAGCCTGGTCCC A T GTPBP10 Ensembl:ENSG00000105793 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:90346754..90346828;chr7:90346750..90346832;chr7:90346748..90346866 26863196 MeRIP-seq:(Medium) rs778015705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956463,Human_RBP_ID_18426042,Human_RBP_ID_19136716 Human_Splice_Rec_886815,Human_Splice_Rec_886829,Human_Splice_Rec_886843,Human_Splice_Rec_886845,Human_Splice_Rec_886861,Human_Splice_Rec_886879 74290 RMVar_ID_74290 Human_SNP_ID_330262889 m1A Human chr7 + 90596112 90596102 90596113 CGTCGAGGGAGGGGCGTGGCGGCGGCAGCAGGAGGGCAGCAGGAGCTGTCAGGCTGGCGGTTCCG CGTCGAGGGAGGGGCGTGGCGGC___________GGCAGCAGGAGCTGTCAGGCTGGCGGTTCCG CGGCAGCAGGAG C CDK14 Ensembl:ENSG00000058091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:90596071..90596179 26863196 MeRIP-seq:(Medium) rs1195739177 Functional Loss DEL dbSNP153 24..34 33 - - - RMVar_hsa_circ_60697,RMVar_hsa_circ_118410,RMVar_hsa_circ_246318 74291 RMVar_ID_74291 Human_SNP_ID_330263031 m1A Human chr7 + 90596445 90596445 90596445 GCCCCCGCCCGCCCAGCTGCGGCCCAGGCCGGAGCGGAGCCTGCCGTCCTCCGCCTGCCTGCTGC GCCCCCGCCCGCCCAGCTGCGGCCCAGGCCGGCGCGGAGCCTGCCGTCCTCCGCCTGCCTGCTGC A C CDK14 Ensembl:ENSG00000058091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:90596396..90596482 26863196 MeRIP-seq:(Medium) rs955844128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60697,RMVar_hsa_circ_118410,RMVar_hsa_circ_246318 74292 RMVar_ID_74292 Human_SNP_ID_330425818 m1A Human chr7 + 91264508 91264508 91264508 GATTGACACAAATGGTCAGGCGGCGGCGGCGGAGAAGGAGGCGGAGGCGCAGGGGGGAGCCGAGC GATTGACACAAATGGTCAGGCGGCGGCGGCGGCGAAGGAGGCGGAGGCGCAGGGGGGAGCCGAGC A C FZD1 Ensembl:ENSG00000157240 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:91264504..91264630 26863196 MeRIP-seq:(Medium) rs961171628 Functional Loss SNV dbSNP153 33..33 33 - - - 74293 RMVar_ID_74293 Human_SNP_ID_330425907 m1A Human chr7 + 91264701 91264701 91264701 TTCTCCCCGCCGCCCGCGCTTCATGAATCGCAAGTTTCCGCGGCGGCGGCGGCTGCGGTACGCAG TTCTCCCCGCCGCCCGCGCTTCATGAATCGCAGGTTTCCGCGGCGGCGGCGGCTGCGGTACGCAG A G FZD1 Ensembl:ENSG00000157240 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:91264612..91264812 32194978 MeRIP-seq:(Medium) rs1563007295 Functional Loss SNV dbSNP153 33..33 33 - - - 74294 RMVar_ID_74294 Human_SNP_ID_330426147 m1A Human chr7 + 91265187 91265187 91265187 CGCCTCAGCAGCAACAGAGCGGGCAGCAGTACAACGGCGAGCGGGGCATCTCCGTCCCGGACCAC CGCCTCAGCAGCAACAGAGCGGGCAGCAGTACCACGGCGAGCGGGGCATCTCCGTCCCGGACCAC A C FZD1 Ensembl:ENSG00000157240 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:91265137..91265219 26863196 MeRIP-seq:(Medium) rs770635483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27533956 74295 RMVar_ID_74295 Human_SNP_ID_330426460 m1A Human chr7 - 91265827 91265827 91265827 ACCAAATGCCAATCCAGGTGCGCGAGAAGCGCAGCTCCTCGGGCCCGAAGTACATGAGCCCATAC ACCAAATGCCAATCCAGGTGCGCGAGAAGCGCCGCTCCTCGGGCCCGAAGTACATGAGCCCATAC T G lnc-MTERF1-5 RNACentral:URS0000D5994E lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:91265755..91265856 32194978 MeRIP-seq:(Medium) rs1014480836 Functional Loss SNV dbSNP153 33..33 33 - - - 74296 RMVar_ID_74296 Human_SNP_ID_330572645 m1A Human chr7 + 91880557 91880557 91880557 CGAAGGCTCTTTCCATCCCTCTTCCTCCTCCAAAGACAAATCTGCAAAGGGCTGCACTGTACAGC CGAAGGCTCTTTCCATCCCTCTTCCTCCTCCACAGACAAATCTGCAAAGGGCTGCACTGTACAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:91880541..91880685 26863196 MeRIP-seq:(Medium) rs1245580350 Functional Loss SNV dbSNP153 33..33 33 - - - 74297 RMVar_ID_74297 Human_SNP_ID_330572665 m1A Human chr7 + 91880655 91880655 91880655 GGAAAGCACAGCCTCACCACCTTCCCAATCTCACCCTGAACTGCACCCATCCACTGTAGTTCGCT GGAAAGCACAGCCTCACCACCTTCCCAATCTCGCCCTGAACTGCACCCATCCACTGTAGTTCGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:91880541..91880676 26863196 MeRIP-seq:(Medium) rs1562847849 Functional Loss SNV dbSNP153 33..33 33 - - - 74298 RMVar_ID_74298 Human_SNP_ID_330587722 m1A Human chr7 - 91940939 91940939 91940939 CCCCGCCCGAAGTGGAAGCAGTCTCCGCGCTCACTGGCGGATCGTCCTCAGCCGCACGGGAAGCG CCCCGCCCGAAGTGGAAGCAGTCTCCGCGCTCGCTGGCGGATCGTCCTCAGCCGCACGGGAAGCG T C lnc-MTERF1-8 RNACentral:URS00008B4BBA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:91940893..91941007 26863196 MeRIP-seq:(Medium) rs1225906353 Functional Loss SNV dbSNP153 33..33 33 - - - 74299 RMVar_ID_74299 Human_SNP_ID_330587723 m1A Human chr7 - 91940939 91940939 91940939 CCCCGCCCGAAGTGGAAGCAGTCTCCGCGCTCACTGGCGGATCGTCCTCAGCCGCACGGGAAGCG CCCCGCCCGAAGTGGAAGCAGTCTCCGCGCTCCCTGGCGGATCGTCCTCAGCCGCACGGGAAGCG T G lnc-MTERF1-8 RNACentral:URS00008B4BBA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:91940893..91941007 26863196 MeRIP-seq:(Medium) rs1225906353 Functional Loss SNV dbSNP153 33..33 33 - - - 74300 RMVar_ID_74300 Human_SNP_ID_330587730 m1A Human chr7 + 91940959 91940959 91940959 ACGATCCGCCAGTGAGCGCGGAGACTGCTTCCACTTCGGGCGGGGGAGCGCCGGACCGAATCGGC ACGATCCGCCAGTGAGCGCGGAGACTGCTTCCGCTTCGGGCGGGGGAGCGCCGGACCGAATCGGC A G AKAP9 Ensembl:ENSG00000127914 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:91940909..91941035 26863196 MeRIP-seq:(Medium) rs1381798502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86997,Human_RBP_ID_4951130,Human_RBP_ID_8914987,Human_RBP_ID_9311331,Human_RBP_ID_18426044,Human_RBP_ID_23080560,Human_RBP_ID_27117559 74301 RMVar_ID_74301 Human_SNP_ID_330587731 m1A Human chr7 + 91940959 91940959 91940959 ACGATCCGCCAGTGAGCGCGGAGACTGCTTCCACTTCGGGCGGGGGAGCGCCGGACCGAATCGGC ACGATCCGCCAGTGAGCGCGGAGACTGCTTCCTCTTCGGGCGGGGGAGCGCCGGACCGAATCGGC A T AKAP9 Ensembl:ENSG00000127914 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:91940909..91941035 26863196 MeRIP-seq:(Medium) rs1381798502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86997,Human_RBP_ID_4951130,Human_RBP_ID_8914987,Human_RBP_ID_9311331,Human_RBP_ID_18426044,Human_RBP_ID_23080560,Human_RBP_ID_27117559 74302 RMVar_ID_74302 Human_SNP_ID_330635267 m1A Human chr7 - 92134324 92134324 92134324 GGCGGCTGGGATGCTGCTGCTGGGCTTGCTGCAGGCGGGTGGGTCGGTGCTGGGCCAGGCGATGG GGCGGCTGGGATGCTGCTGCTGGGCTTGCTGCTGGCGGGTGGGTCGGTGCTGGGCCAGGCGATGG T A AC000120.3,AC000120.4,CYP51A1 Ensembl:ENSG00000285772,Ensembl:ENSG00000285953,Ensembl:ENSG00000001630 Protein coding,Protein coding,Protein coding intron,intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:92134151..92134500;chr7:92134226..92134500 26863196 MeRIP-seq:(Medium) rs1257617460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82251,Human_RBP_ID_689774,Human_RBP_ID_792654,Human_RBP_ID_956278,Human_RBP_ID_4955860,Human_RBP_ID_5328492,Human_RBP_ID_7767639,Human_RBP_ID_9337222,Human_RBP_ID_18472339,Human_RBP_ID_22110918,Human_RBP_ID_22463170,Human_RBP_ID_22774660,Human_RBP_ID_23080092,Human_RBP_ID_24230994 RMVar_hsa_circ_125147,RMVar_hsa_circ_246406 74303 RMVar_ID_74303 Human_SNP_ID_330662688 m1A Human chr7 + 92245855 92245855 92245855 TCAGCACCATTCACCCCTCACCCTCTCCCGAAACTACGGGGTCCCAGGTCTTCAAAGGCCTTAGC TCAGCACCATTCACCCCTCACCCTCTCCCGAATCTACGGGGTCCCAGGTCTTCAAAGGCCTTAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:92245619..92245888 26863196 MeRIP-seq:(Medium) rs1170099903 Functional Loss SNV dbSNP153 33..33 33 - - - 74304 RMVar_ID_74304 Human_SNP_ID_330662806 m1A Human chr7 + 92246153 92246153 92246153 GGGAAGAGGGCGGCCGGGGCTGCGAGCGCGCAAGGCTGGAACATGAGCCGGGCTTGACCGCGAGG GGGAAGAGGGCGGCCGGGGCTGCGAGCGCGCAGGGCTGGAACATGAGCCGGGCTTGACCGCGAGG A G ANKIB1 Ensembl:ENSG00000001629 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:92245996..92294897 26863196 MeRIP-seq:(Medium) rs1224253033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18105717 74305 RMVar_ID_74305 Human_SNP_ID_330709751 m1A Human chr7 - 92447524 92447524 92447524 AGCGGGTTCCGCCGGCTCCGCAGGCGGAGGCCAGGATTCCCTGGCCCGAGGCACTGGGAAGCAGG AGCGGGTTCCGCCGGCTCCGCAGGCGGAGGCCGGGATTCCCTGGCCCGAGGCACTGGGAAGCAGG T C TMBIM7P Ensembl:ENSG00000230927 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:92447452..92447656 26863196 MeRIP-seq:(Medium) rs192745223 Functional Loss SNV dbSNP153 33..33 33 - - - 74306 RMVar_ID_74306 Human_SNP_ID_330709755 m1A Human chr7 + 92447540 92447531 92447540 TCGGGCCAGGGAATCCTGGCCTCCGCCTGCGGAGCCGGCGGAACCCGCTTCCCGCCTCCACGGGG TCGGGCCAGGGAATCCTGGCCTCC_________GCCGGCGGAACCCGCTTCCCGCCTCCACGGGG CGCCTGCGGA C GATAD1 Ensembl:ENSG00000157259 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:92447494..92447635 26863196 MeRIP-seq:(Medium) rs1475704803 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4956465,Human_RBP_ID_9337225,Human_RBP_ID_18426045 74307 RMVar_ID_74307 Human_SNP_ID_330709760 m1A Human chr7 + 92447540 92447540 92447540 TCGGGCCAGGGAATCCTGGCCTCCGCCTGCGGAGCCGGCGGAACCCGCTTCCCGCCTCCACGGGG TCGGGCCAGGGAATCCTGGCCTCCGCCTGCGGGGCCGGCGGAACCCGCTTCCCGCCTCCACGGGG A G GATAD1 Ensembl:ENSG00000157259 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:92447494..92447635 26863196 MeRIP-seq:(Medium) rs1041147485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956465,Human_RBP_ID_9337225,Human_RBP_ID_18426045 74308 RMVar_ID_74308 Human_SNP_ID_330709766 m1A Human chr7 + 92447549 92447546 92447549 GGAATCCTGGCCTCCGCCTGCGGAGCCGGCGGAACCCGCTTCCCGCCTCCACGGGGCAGCGCCAG GGAATCCTGGCCTCCGCCTGCGGAGCCGGC___ACCCGCTTCCCGCCTCCACGGGGCAGCGCCAG CGGA C GATAD1 Ensembl:ENSG00000157259 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:92447499..92447925;chr7:92447498..92447640 26863196 MeRIP-seq:(Medium) rs1159195878 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_794367,Human_RBP_ID_4956466,Human_RBP_ID_9337225,Human_RBP_ID_18426045 74309 RMVar_ID_74309 Human_SNP_ID_330718611 m1A Human chr7 - 92482720 92482720 92482720 ACATTTTAACCAAATTATCTGCTTCCCCGACTATTCCTGGGCTACAGCCACATCTCCTTGCCGCC ACATTTTAACCAAATTATCTGCTTCCCCGACTGTTCCTGGGCTACAGCCACATCTCCTTGCCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:92482675..92482755 26863196 MeRIP-seq:(Medium) rs1311394364 Functional Loss SNV dbSNP153 33..33 33 - - - 74310 RMVar_ID_74310 Human_SNP_ID_330765789 m1A Human chr7 - 92682159 92682159 92682159 TGGTGAGCACAGCTTCAGATGCAGTAAAGAAGACAGAGTGGCAGGGGGCATGTTGGCAGGAAAAG TGGTGAGCACAGCTTCAGATGCAGTAAAGAAGGCAGAGTGGCAGGGGGCATGTTGGCAGGAAAAG T C CDK6 Ensembl:ENSG00000105810 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:92681992..92682266 26863196 MeRIP-seq:(Medium) rs1347728537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16943,RMVar_hsa_circ_94806,RMVar_hsa_circ_246510,RMVar_hsa_circ_246515,RMVar_hsa_circ_275010,RMVar_hsa_circ_373046,RMVar_hsa_circ_288604,RMVar_hsa_circ_246516,RMVar_hsa_circ_246514 74311 RMVar_ID_74311 Human_SNP_ID_330775214 m1A Human chr7 + 92724081 92724081 92724081 AAGGAGACAAGTTCCTTCCATCTACTCCCCTGATGACTCTCTGGATCACAAAGCCTATTCAAGCT AAGGAGACAAGTTCCTTCCATCTACTCCCCTGGTGACTCTCTGGATCACAAAGCCTATTCAAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:92724031..92724168 26863196 MeRIP-seq:(Medium) rs1218929320 Functional Loss SNV dbSNP153 33..33 33 - - - 74312 RMVar_ID_74312 Human_SNP_ID_330792008 m1A Human chr7 - 92800038 92800038 92800038 AGCTAGTTAGATGTGTAGGTGAACAGAGCTGTAGGGTCAACAAGATGAATTATGGTTTTATGCTT AGCTAGTTAGATGTGTAGGTGAACAGAGCTGTGGGGTCAACAAGATGAATTATGGTTTTATGCTT T C CDK6 Ensembl:ENSG00000105810 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:92800022..92800117 26863196 MeRIP-seq:(Medium) rs940115217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3112921 RMVar_hsa_circ_16943,RMVar_hsa_circ_94806,RMVar_hsa_circ_246510,RMVar_hsa_circ_373046,RMVar_hsa_circ_246516,RMVar_hsa_circ_336431 74313 RMVar_ID_74313 Human_SNP_ID_330799426 m1A Human chr7 - 92833403 92833403 92833403 AAGCTAGACCGATCTCCGGGGAGCCCCGGAGTAGGCGAGCGGCGGCCGCCAGCTAGTTGAGCGCA AAGCTAGACCGATCTCCGGGGAGCCCCGGAGTGGGCGAGCGGCGGCCGCCAGCTAGTTGAGCGCA T C CDK6 Ensembl:ENSG00000105810 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:92833300..92833650 26863196 MeRIP-seq:(Medium) rs1171081628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843662,Human_RBP_ID_956246,Human_RBP_ID_4955864,Human_RBP_ID_5533896,Human_RBP_ID_9311333,Human_RBP_ID_22463615,Human_RBP_ID_24536799 RMVar_hsa_circ_16943,RMVar_hsa_circ_94806,RMVar_hsa_circ_246510,RMVar_hsa_circ_111892,RMVar_hsa_circ_373046,RMVar_hsa_circ_246516,RMVar_hsa_circ_336431,RMVar_hsa_circ_246519 74314 RMVar_ID_74314 Human_SNP_ID_330817979 m1A Human chr7 + 92917138 92917138 92917138 CCACTTTGAGATTAAAACCCCTGAAAGCTGCCACACCGTGAAAACAAGGCCTCCTTCACATTAAA CCACTTTGAGATTAAAACCCCTGAAAGCTGCCGCACCGTGAAAACAAGGCCTCCTTCACATTAAA A G CDK6-AS1 Ensembl:ENSG00000237819 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:92917043..92917139 26863196 MeRIP-seq:(Medium) rs561139877 Functional Loss SNV dbSNP153 33..33 33 - - - 74315 RMVar_ID_74315 Human_SNP_ID_330894539 m1A Human chr7 + 93235167 93235166 93235167 GATATTTGGGAAGGAGCATTTCCAGTGGAAGGAAAGGCAAATGCAGAGGTCCTGAGGCAGGAGCT GATATTTGGGAAGGAGCATTTCCAGTGGAAGG_AAGGCAAATGCAGAGGTCCTGAGGCAGGAGCT GA G VPS50 Ensembl:ENSG00000004766 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:93235117..93235256 26863196 MeRIP-seq:(Medium) rs1214186189 Functional Loss DEL dbSNP153 33..33 33 - - - 74316 RMVar_ID_74316 Human_SNP_ID_331052914 m1A Human chr7 + 93922091 93922091 93922091 TTTCGGGACGCGCCGAGCTTCGCCGCTCTTCCAGCGGCTCCGCTGCCAGAGCTAGCCCGAGCCCG TTTCGGGACGCGCCGAGCTTCGCCGCTCTTCCGGCGGCTCCGCTGCCAGAGCTAGCCCGAGCCCG A G GNG11 Ensembl:ENSG00000127920 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:93921944..93922093 32194978 MeRIP-seq:(Medium) rs570664184 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_340 74317 RMVar_ID_74317 Human_SNP_ID_331063104 m1A Human chr7 + 93964221 93964221 93964221 TGCTGAGGTTTGAGATATGAATTTCTCACCCAAGTAGTGAGCATAGTACCCAATAGCTAGTTTTT TGCTGAGGTTTGAGATATGAATTTCTCACCCAGGTAGTGAGCATAGTACCCAATAGCTAGTTTTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:93964181..93964268 26863410 MeRIP-seq:(Medium) rs1219672458 Functional Loss SNV dbSNP153 33..33 33 - - - 74318 RMVar_ID_74318 Human_SNP_ID_331069535 m1A Human chr7 + 93993848 93993848 93993848 TACCACAAACTGGCTGACTACTTCAAGAGCTCAGAGTCAGGCTCTCCAGGCATTCTGTTACTCTC TACCACAAACTGGCTGACTACTTCAAGAGCTCCGAGTCAGGCTCTCCAGGCATTCTGTTACTCTC A C BET1-AS1 Ensembl:ENSG00000236861 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:93993798..93993949 32194978 MeRIP-seq:(Medium) rs528151776 Functional Loss SNV dbSNP153 33..33 33 - - - 74319 RMVar_ID_74319 Human_SNP_ID_331069536 m1A Human chr7 + 93993848 93993848 93993848 TACCACAAACTGGCTGACTACTTCAAGAGCTCAGAGTCAGGCTCTCCAGGCATTCTGTTACTCTC TACCACAAACTGGCTGACTACTTCAAGAGCTCTGAGTCAGGCTCTCCAGGCATTCTGTTACTCTC A T BET1-AS1 Ensembl:ENSG00000236861 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:93993798..93993949 32194978 MeRIP-seq:(Medium) rs528151776 Functional Loss SNV dbSNP153 33..33 33 - - - 74320 RMVar_ID_74320 Human_SNP_ID_331192665 m1A Human chr7 + 94509873 94509873 94509873 CACGGCGGAGCAGCGGCGGCGGGGCTGGGGGGAGGCCGCCGAGTCGGCCGCGGCCGAGGAGGGGC CACGGCGGAGCAGCGGCGGCGGGGCTGGGGGGGGGCCGCCGAGTCGGCCGCGGCCGAGGAGGGGC A G CASD1 Ensembl:ENSG00000127995 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:94509812..94510065 26863196 MeRIP-seq:(Medium) rs939043585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955871,Human_RBP_ID_9354766,Human_RBP_ID_18426048,Human_RBP_ID_22463616 74321 RMVar_ID_74321 Human_SNP_ID_331192668 m1A Human chr7 + 94509882 94509882 94509882 GCAGCGGCGGCGGGGCTGGGGGGAGGCCGCCGAGTCGGCCGCGGCCGAGGAGGGGCAGGCGGAGG GCAGCGGCGGCGGGGCTGGGGGGAGGCCGCCGGGTCGGCCGCGGCCGAGGAGGGGCAGGCGGAGG A G CASD1 Ensembl:ENSG00000127995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:94509786..94510115 26863196 MeRIP-seq:(Medium) rs1312265253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955871,Human_RBP_ID_9354766,Human_RBP_ID_18426048,Human_RBP_ID_22463616 74322 RMVar_ID_74322 Human_SNP_ID_331228051 m1A Human chr7 - 94663518 94663518 94663518 GACACACGCACTCTTATGGCCGGTGTGCTTGGAGTTGTTGTTGTTGTTGTTGTTGGGGGGAGGGG GACACACGCACTCTTATGGCCGGTGTGCTTGGTGTTGTTGTTGTTGTTGTTGTTGGGGGGAGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:94663468..94663790 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - RMVar_hsa_circ_246676 74323 RMVar_ID_74323 Human_SNP_ID_331398808 m1A Human chr7 + 95405462 95405462 95405462 TTGGCATAAACTGTAGTCACTGTAGGCTTCTCAGATAGAATGTTCTGGATGCGGAGAACCTATTC TTGGCATAAACTGTAGTCACTGTAGGCTTCTCTGATAGAATGTTCTGGATGCGGAGAACCTATTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:95405411..95407005 32194978 MeRIP-seq:(Medium) rs759001410 Functional Loss SNV dbSNP153 33..33 33 - - - 74324 RMVar_ID_74324 Human_SNP_ID_331400325 m1A Human chr7 - 95412472 95412472 95412472 TTTAACATTTTTCACCGTTTTGGAAAGGGTCTAAAATTCCCAGGACTCCACAGCTTTGCACCAGA TTTAACATTTTTCACCGTTTTGGAAAGGGTCTCAAATTCCCAGGACTCCACAGCTTTGCACCAGA T G PON2 Ensembl:ENSG00000105854 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:95412421..95412788 32194978 MeRIP-seq:(Medium) rs1238402741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83507,Human_RBP_ID_3116982,Human_RBP_ID_16252791,Human_RBP_ID_22463624,Human_RBP_ID_22620677,Human_RBP_ID_26125905 Human_Splice_Rec_892106,Human_Splice_Rec_892122,Human_Splice_Rec_892138,Human_Splice_Rec_892154,Human_Splice_Rec_892170,Human_Splice_Rec_892194,Human_Splice_Rec_892210,Human_Splice_Rec_892220,Human_Splice_Rec_892236,Human_Splice_Rec_892246,Human_Splice_Rec_892258 Human_miRNA_ID_2039625,Human_miRNA_ID_3018607 RMVar_hsa_circ_126524,RMVar_hsa_circ_246691,RMVar_hsa_circ_95668,RMVar_hsa_circ_246692 74325 RMVar_ID_74325 Human_SNP_ID_331608069 m1A Human chr7 - 96296942 96296942 96296942 AACATTTTTATGTTTATTTATAGGTGGCTTTAACCAAGAGAGCAGATCCAGCTGAGCTTAGAACA AACATTTTTATGTTTATTTATAGGTGGCTTTAGCCAAGAGAGCAGATCCAGCTGAGCTTAGAACA T C SLC25A13 Ensembl:ENSG00000004864 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:96296901..96309593 26863410 MeRIP-seq:(Medium) rs1223102191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82294,Human_RBP_ID_4956471,Human_RBP_ID_16254297,Human_RBP_ID_19135103 Human_Splice_Rec_892634,Human_Splice_Rec_892635,Human_Splice_Rec_892668,Human_Splice_Rec_892669,Human_Splice_Rec_892728,Human_Splice_Rec_892729,Human_Splice_Rec_892736 RMVar_hsa_circ_112037,RMVar_hsa_circ_41980,RMVar_hsa_circ_74957,RMVar_hsa_circ_246721,RMVar_hsa_circ_64415,RMVar_hsa_circ_246726,RMVar_hsa_circ_274582,RMVar_hsa_circ_246727 74326 RMVar_ID_74326 Human_SNP_ID_331608071 m1A Human chr7 + 96296950 96296949 96296950 GCTCAGCTGGATCTGCTCTCTTGGTTAAAGCCACCTATAAATAAACATAAAAATGTTTATGTTAT GCTCAGCTGGATCTGCTCTCTTGGTTAAAGCC_CCTATAAATAAACATAAAAATGTTTATGTTAT CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:96296876..96309593 26863196 MeRIP-seq:(Medium) rs1309175371 Functional Loss DEL dbSNP153 33..33 33 - - - 74327 RMVar_ID_74327 Human_SNP_ID_331613750 m1A Human chr7 + 96321834 96321834 96321834 AGCCGCAAGGTGGAACGGCTGCCCGGCACCCCATTTTGCTCCGCCTGTGGCACCAACCCAGACAC AGCCGCAAGGTGGAACGGCTGCCCGGCACCCCGTTTTGCTCCGCCTGTGGCACCAACCCAGACAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:96321817..96321948 26863196 MeRIP-seq:(Medium) rs1031811066 Functional Loss SNV dbSNP153 33..33 33 - - - 74328 RMVar_ID_74328 Human_SNP_ID_331613856 m1A Human chr7 - 96322026 96322026 96322026 CCCCACCGCCGCCGCCGCCGGGACTAGAAGTGAGCCGCCCGGGTCCCAAACGCCAGCCAGCCAGT CCCCACCGCCGCCGCCGCCGGGACTAGAAGTGGGCCGCCCGGGTCCCAAACGCCAGCCAGCCAGT T C SLC25A13 Ensembl:ENSG00000004864 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:96322003..96322094 26863410 MeRIP-seq:(Medium) rs779638076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956472 Human_Splice_Rec_892633,Human_Splice_Rec_892667,Human_Splice_Rec_892727 74329 RMVar_ID_74329 Human_SNP_ID_331697350 m1A Human chr7 - 96688896 96688896 96688896 CATAGCATCCAGAAGAAGTGTTGAAGTAACCTAAACTTGACCTGCTTAATACATTCTAGGGCAGA CATAGCATCCAGAAGAAGTGTTGAAGTAACCTGAACTTGACCTGCTTAATACATTCTAGGGCAGA T C SEM1 Ensembl:ENSG00000127922 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:96688826..96688975 26863196 MeRIP-seq:(Medium) rs762101017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690550,Human_RBP_ID_952593,Human_RBP_ID_2049641,Human_RBP_ID_9341661,Human_RBP_ID_9403616,Human_RBP_ID_17314660,Human_RBP_ID_17665046,Human_RBP_ID_22326588,Human_RBP_ID_22464121,Human_RBP_ID_23215559,Human_RBP_ID_24233023,Human_RBP_ID_24390043,Human_RBP_ID_26772222,Human_RBP_ID_27830522 Human_Splice_Rec_892870,Human_Splice_Rec_892872 RMVar_hsa_circ_93506,RMVar_hsa_circ_97745,RMVar_hsa_circ_114018,RMVar_hsa_circ_246732,RMVar_hsa_circ_246733,RMVar_hsa_circ_246734 74330 RMVar_ID_74330 Human_SNP_ID_331702259 m1A Human chr7 - 96709806 96709806 96709806 TGGCGTTTCCTTGAGGAAGAGTGAGGGTTCCAACTTTTCTGCTTATCTGGGAGGTGTTGGGCGCG TGGCGTTTCCTTGAGGAAGAGTGAGGGTTCCAGCTTTTCTGCTTATCTGGGAGGTGTTGGGCGCG T C SEM1 Ensembl:ENSG00000127922 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:96709695..96709850 26863196 MeRIP-seq:(Medium) rs1286770262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84272,Human_RBP_ID_690558,Human_RBP_ID_3858824,Human_RBP_ID_4952628,Human_RBP_ID_8674739,Human_RBP_ID_9215444,Human_RBP_ID_24233084 RMVar_hsa_circ_97745,RMVar_hsa_circ_246734 74331 RMVar_ID_74331 Human_SNP_ID_331702260 m1A Human chr7 + 96709810 96709810 96709810 CCCAACACCTCCCAGATAAGCAGAAAAGTTGGAACCCTCACTCTTCCTCAAGGAAACGCCACCGT CCCAACACCTCCCAGATAAGCAGAAAAGTTGGCACCCTCACTCTTCCTCAAGGAAACGCCACCGT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:96709635..96709875;chr7:96709645..96709875 26863196 MeRIP-seq:(Medium) rs775752690 Functional Loss SNV dbSNP153 33..33 33 - - - 74332 RMVar_ID_74332 Human_SNP_ID_331798297 m1A Human chr7 - 97117749 97117749 97117749 GCAGCTGCAAGACGCGCTTGTACAATGCCCGGACTCGAGAAACGTGCCGCCCCGGCATAGCGCCC GCAGCTGCAAGACGCGCTTGTACAATGCCCGGGCTCGAGAAACGTGCCGCCCCGGCATAGCGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:97117701..97117875 26863196 MeRIP-seq:(Medium) rs370361430 Functional Loss SNV dbSNP153 33..33 33 - - - 74333 RMVar_ID_74333 Human_SNP_ID_331798312 m1A Human chr7 + 97117764 97117764 97117764 GCGGCACGTTTCTCGAGTCCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC GCGGCACGTTTCTCGAGTCCGGGCATTGTACACGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC A C SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:97117701..97117866 26863196 MeRIP-seq:(Medium) rs754390024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1689856,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_16256731,Human_RBP_ID_17314661,Human_RBP_ID_17426998,Human_RBP_ID_18426052 Human_miRNA_ID_1428735,Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 74334 RMVar_ID_74334 Human_SNP_ID_331798313 m1A Human chr7 + 97117764 97117764 97117764 GCGGCACGTTTCTCGAGTCCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC GCGGCACGTTTCTCGAGTCCGGGCATTGTACAGGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC A G SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:97117701..97117866 26863196 MeRIP-seq:(Medium) rs754390024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1689856,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_16256731,Human_RBP_ID_17314661,Human_RBP_ID_17426998,Human_RBP_ID_18426052 Human_miRNA_ID_1428735,Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 74335 RMVar_ID_74335 Human_SNP_ID_331798322 m1A Human chr7 + 97117782 97117782 97117782 CCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCCCGGACCTCAAATCCCTGG CCGGGCATTGTACAAGCGCGTCTTGCAGCTGCGCCGTGTTCTGCCCCCGGACCTCAAATCCCTGG A G SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:97117733..97117842 26863196 MeRIP-seq:(Medium) rs758025027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690573,Human_RBP_ID_1689856,Human_RBP_ID_4952687,Human_RBP_ID_5328496,Human_RBP_ID_8913296,Human_RBP_ID_9337231,Human_RBP_ID_17314661,Human_RBP_ID_18426052 Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 74336 RMVar_ID_74336 Human_SNP_ID_331798323 m1A Human chr7 + 97117782 97117782 97117782 CCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCCCGGACCTCAAATCCCTGG CCGGGCATTGTACAAGCGCGTCTTGCAGCTGCTCCGTGTTCTGCCCCCGGACCTCAAATCCCTGG A T SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:97117733..97117842 26863196 MeRIP-seq:(Medium) rs758025027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690573,Human_RBP_ID_1689856,Human_RBP_ID_4952687,Human_RBP_ID_5328496,Human_RBP_ID_8913296,Human_RBP_ID_9337231,Human_RBP_ID_17314661,Human_RBP_ID_18426052 Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 74337 RMVar_ID_74337 Human_SNP_ID_331798340 m1A Human chr7 + 97117806 97117806 97117806 GCAGCTGCACCGTGTTCTGCCCCCGGACCTCAAATCCCTGGGCGACCAGTACGTGAAAGACGAAT GCAGCTGCACCGTGTTCTGCCCCCGGACCTCAGATCCCTGGGCGACCAGTACGTGAAAGACGAAT A G SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:97117726..97117850 26863410 MeRIP-seq:(Medium) rs775543999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690573,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_17314661,Human_RBP_ID_18426052,Human_RBP_ID_24233133,Human_RBP_ID_27534217 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 74338 RMVar_ID_74338 Human_SNP_ID_331798343 m1A Human chr7 - 97117812 97117812 97117812 TCCTAAATTCGTCTTTCACGTACTGGTCGCCCAGGGATTTGAGGTCCGGGGGCAGAACACGGTGC TCCTAAATTCGTCTTTCACGTACTGGTCGCCCGGGGATTTGAGGTCCGGGGGCAGAACACGGTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:97117764..97117863 32194978 MeRIP-seq:(Medium) rs765043714 Functional Loss SNV dbSNP153 33..33 33 - - - 74339 RMVar_ID_74339 Human_SNP_ID_331814133 m1A Human chr7 - 97181077 97181077 97181077 TTAAGTTTTTCTTCTGGGAGGAAGGTGCCAAAACATGCTTTTCCAGTTGAATTTTGTCTGTTTTC TTAAGTTTTTCTTCTGGGAGGAAGGTGCCAAACCATGCTTTTCCAGTTGAATTTTGTCTGTTTTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:97181027..97181126 32194978 MeRIP-seq:(Medium) rs1400358621 Functional Loss SNV dbSNP153 33..33 33 - - - 74340 RMVar_ID_74340 Human_SNP_ID_331974392 m1A Human chr7 + 97852269 97852269 97852269 CACATTACAGCATAAAGACCACCTAAGCTTTGACAGCTGACTTGTAGTGGGTCAGCGTGCGGGCA CACATTACAGCATAAAGACCACCTAAGCTTTGCCAGCTGACTTGTAGTGGGTCAGCGTGCGGGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:97852222..97852378 26863196 MeRIP-seq:(Medium) rs879056597 Functional Loss SNV dbSNP153 33..33 33 - - - 74341 RMVar_ID_74341 Human_SNP_ID_331974407 m1A Human chr7 - 97852317 97852317 97852317 GCTGAGCCATTACTGGATGCCCAAGTGGATCAATGCCACTGACCCTTCTGCCCGCACGCTGACCC GCTGAGCCATTACTGGATGCCCAAGTGGATCAGTGCCACTGACCCTTCTGCCCGCACGCTGACCC T C AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding exon,CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs751735389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690616,Human_RBP_ID_1144567,Human_RBP_ID_1689917,Human_RBP_ID_5153224,Human_RBP_ID_5270027,Human_RBP_ID_7779515,Human_RBP_ID_8220628,Human_RBP_ID_9215489,Human_RBP_ID_9263466,Human_RBP_ID_17315649,Human_RBP_ID_17426999,Human_RBP_ID_17664284,Human_RBP_ID_23215563,Human_RBP_ID_26831421 RMVar_hsa_circ_108188,RMVar_hsa_circ_246747 74342 RMVar_ID_74342 Human_SNP_ID_331978791 m1A Human chr7 - 97871831 97871831 97871831 TTTCACCTTCAACTGCCCCCCTCCTCACCTGGACCGCTCACCCTCCTCCTCCCCTCTCACCCCGC TTTCACCTTCAACTGCCCCCCTCCTCACCTGGGCCGCTCACCCTCCTCCTCCCCTCTCACCCCGC T C AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:97871824..97871935 26863196 MeRIP-seq:(Medium) rs937180227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868231,Human_RBP_ID_5090573,Human_RBP_ID_5657916,Human_RBP_ID_7775135,Human_RBP_ID_17093320,Human_RBP_ID_17427010,Human_RBP_ID_18960207,Human_RBP_ID_22112388,Human_RBP_ID_24563103,Human_RBP_ID_26793567,Human_RBP_ID_27534230 RMVar_hsa_circ_86071,RMVar_hsa_circ_246750 74343 RMVar_ID_74343 Human_SNP_ID_331979000 m1A Human chr7 - 97872347 97872347 97872347 CCACATCACCCTGACCTGCTTACGCCCAGGTGAGCCGGGTCCTGCGCCCCGTGCCCTGCGCCCCG CCACATCACCCTGACCTGCTTACGCCCAGGTGCGCCGGGTCCTGCGCCCCGTGCCCTGCGCCCCG T G AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:97872215..97872400 26863196 MeRIP-seq:(Medium) rs1330077824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253993,Human_RBP_ID_955405,Human_RBP_ID_4956474,Human_RBP_ID_5090577,Human_RBP_ID_5402218,Human_RBP_ID_19135110,Human_RBP_ID_26793571 74344 RMVar_ID_74344 Human_SNP_ID_331992351 m1A Human chr7 + 97928390 97928390 97928390 GGCGGAGCTGGGGCGTCTGAGCGCGGGCTCGGAGGGTCCGCGCGGCGCGGAGGTGGGCACCGGGG GGCGGAGCTGGGGCGTCTGAGCGCGGGCTCGGTGGGTCCGCGCGGCGCGGAGGTGGGCACCGGGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:97928311..97928406 26863410 MeRIP-seq:(Medium) rs188295221 Functional Loss SNV dbSNP153 33..33 33 - - - 74345 RMVar_ID_74345 Human_SNP_ID_332004367 m1A Human chr7 - 97972163 97972163 97972163 CCTGCCGGCGCTGCTGAGTTTCTTCATCTACAACCCGCGCTTCTGGCCGCGGGAAGGAGAGGTAT CCTGCCGGCGCTGCTGAGTTTCTTCATCTACAGCCCGCGCTTCTGGCCGCGGGAAGGAGAGGTAT T C AC079781.5,AC004967.1 Ensembl:ENSG00000284707,Ensembl:ENSG00000243554 lincRNA,Pseudogene exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:97972132..97972313 26863196 MeRIP-seq:(Medium) rs1310834601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690672,Human_RBP_ID_4952801,Human_RBP_ID_5104673,Human_RBP_ID_5404229,Human_RBP_ID_5513837,Human_RBP_ID_8674890,Human_RBP_ID_9217216,Human_RBP_ID_17429626,Human_RBP_ID_19019844,Human_RBP_ID_23297314 Human_Splice_Rec_893203,Human_Splice_Rec_893237,Human_Splice_Rec_893299 Human_miRNA_ID_1844068,Human_miRNA_ID_2250035 RMVar_hsa_circ_122877,RMVar_hsa_circ_246754 74346 RMVar_ID_74346 Human_SNP_ID_332004380 m1A Human chr7 + 97972193 97972193 97972193 GGTTGTAGATGAAGAAACTCAGCAGCGCCGGCAGGAACTGCTTCTCCTGGGCCGCCGAGGGCCCG GGTTGTAGATGAAGAAACTCAGCAGCGCCGGCGGGAACTGCTTCTCCTGGGCCGCCGAGGGCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr7:97972144..97972333;chr7:97972143..97972316 26863196 MeRIP-seq:(Medium) rs1186212797 Functional Loss SNV dbSNP153 33..33 33 - - - 74347 RMVar_ID_74347 Human_SNP_ID_332055237 m1A Human chr7 - 98168234 98168234 98168234 TCTTGTGCCTTTCTAAGCTCAGTCCTCTCGAGAGTCCATCTCTTCTCTCTGCTCTGGCCCCAAAC TCTTGTGCCTTTCTAAGCTCAGTCCTCTCGAGGGTCCATCTCTTCTCTCTGCTCTGGCCCCAAAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:98168187..98168309 26863196 MeRIP-seq:(Medium) rs1391705870 Functional Loss SNV dbSNP153 33..33 33 - - - 74348 RMVar_ID_74348 Human_SNP_ID_332073146 m1A Human chr7 + 98232787 98232785 98232788 ACACAGCAGGCGCTCAATGAATGATTGCTGGAAAAAAAAAAAAAATGCATGCGCAGCCACCGGGG ACACAGCAGGCGCTCAATGAATGATTGCTGG___AAAAAAAAAAATGCATGCGCAGCCACCGGGG GAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:98232780..98232904 26863196 MeRIP-seq:(Medium) rs139511001 Functional Loss DEL dbSNP153 32..34 33 - - - 74349 RMVar_ID_74349 Human_SNP_ID_332073147 m1A Human chr7 + 98232787 98232785 98232788 ACACAGCAGGCGCTCAATGAATGATTGCTGGAAAAAAAAAAAAAATGCATGCGCAGCCACCGGGG ACACAGCAGGCGCTCAATGAATGATTGCTGGA__AAAAAAAAAAATGCATGCGCAGCCACCGGGG GAAA GA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:98232780..98232904 26863196 MeRIP-seq:(Medium) rs139511001 Functional Loss DEL dbSNP153 33..34 33 - - - 74350 RMVar_ID_74350 Human_SNP_ID_332073153 m1A Human chr7 + 98232787 98232787 98232787 ACACAGCAGGCGCTCAATGAATGATTGCTGGAAAAAAAAAAAAAATGCATGCGCAGCCACCGGGG ACACAGCAGGCGCTCAATGAATGATTGCTGGAGAAAAAAAAAAAATGCATGCGCAGCCACCGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:98232780..98232904 26863196 MeRIP-seq:(Medium) rs1486188338 Functional Loss SNV dbSNP153 33..33 33 - - - 74351 RMVar_ID_74351 Human_SNP_ID_332074935 m1A Human chr7 - 98238483 98238483 98238483 CGACCAGGTGTGCACGTGGGTCTGCAGCCCCTAAACAGCAGGGGTCTCAGAATGGGGGCTCCTGA CGACCAGGTGTGCACGTGGGTCTGCAGCCCCTGAACAGCAGGGGTCTCAGAATGGGGGCTCCTGA T C TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:98238475..98238580 26863196 MeRIP-seq:(Medium) rs1439847836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60094,RMVar_hsa_circ_515,RMVar_hsa_circ_370245,RMVar_hsa_circ_246773,RMVar_hsa_circ_246775,RMVar_hsa_circ_378216,RMVar_hsa_circ_246776 74352 RMVar_ID_74352 Human_SNP_ID_332078530 m1A Human chr7 - 98251517 98251517 98251517 GGACCCTGATGTCGCTTTTGAACAGCCCCTGCACCTGGCAGCCAGCGAGCTACTGTAGTAGGCAT GGACCCTGATGTCGCTTTTGAACAGCCCCTGCCCCTGGCAGCCAGCGAGCTACTGTAGTAGGCAT T G TECPR1 Ensembl:ENSG00000205356 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:98251468..98251577 26863196 MeRIP-seq:(Medium) rs1048352450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4953096 Human_Splice_Rec_893354,Human_Splice_Rec_893492,Human_Splice_Rec_893493,Human_Splice_Rec_893500,Human_Splice_Rec_893501,Human_Splice_Rec_893506,Human_Splice_Rec_893512,Human_Splice_Rec_893513,Human_Splice_Rec_893518 RMVar_hsa_circ_60094 74353 RMVar_ID_74353 Human_SNP_ID_332081966 m1A Human chr7 - 98265583 98265583 98265583 ACCATGTTGGCCAGGCTGGTCTCGCACTCCCGACCTTGTGATCCACCCGCCTCGGACTCCCAAAG ACCATGTTGGCCAGGCTGGTCTCGCACTCCCGTCCTTGTGATCCACCCGCCTCGGACTCCCAAAG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:98265535..98265622 26863410 MeRIP-seq:(Medium) rs6970395 Functional Loss SNV dbSNP153 33..33 33 - - - 74354 RMVar_ID_74354 Human_SNP_ID_332081967 m1A Human chr7 - 98265583 98265583 98265583 ACCATGTTGGCCAGGCTGGTCTCGCACTCCCGACCTTGTGATCCACCCGCCTCGGACTCCCAAAG ACCATGTTGGCCAGGCTGGTCTCGCACTCCCGCCCTTGTGATCCACCCGCCTCGGACTCCCAAAG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:98265535..98265622 26863410 MeRIP-seq:(Medium) rs6970395 Functional Loss SNV dbSNP153 33..33 33 - - - 74355 RMVar_ID_74355 Human_SNP_ID_332086404 m1A Human chr7 - 98281716 98281716 98281716 CCCCGGCGGGGGACGCGGCGGCGGCGGCGGGGACGCGGCGGACCGGGTGGCTCGGGCCCCTCTGA CCCCGGCGGGGGACGCGGCGGCGGCGGCGGGGGCGCGGCGGACCGGGTGGCTCGGGCCCCTCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:98252376..98282379;chr7:98252388..98282379;chr7:98252396..98281857 26863196 MeRIP-seq:(Medium) rs956332575 Functional Loss SNV dbSNP153 33..33 33 - - - 74356 RMVar_ID_74356 Human_SNP_ID_332086446 m1A Human chr7 - 98281797 98281797 98281797 GCGGCCGCTCCTGCAGCAGCGGCTTGTGGTCCATGGCGGCCCGGCCGCGCCCGCCGCTCCGGCCC GCGGCCGCTCCTGCAGCAGCGGCTTGTGGTCCGTGGCGGCCCGGCCGCGCCCGCCGCTCCGGCCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr7:98281626..98282379;chr7:98281701..98281866 26863410 MeRIP-seq:(Medium) rs1248409767 Functional Loss SNV dbSNP153 33..33 33 - - - 74357 RMVar_ID_74357 Human_SNP_ID_332086495 m1A Human chr7 + 98281926 98281926 98281926 CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTACCTCGTCACAGGTGGGCCCGTAACCAACTTTC CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTCCCTCGTCACAGGTGGGCCCGTAACCAACTTTC A C BRI3 Ensembl:ENSG00000164713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:98281876..98281950 26863196 MeRIP-seq:(Medium) rs1469279706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17427020 Human_Splice_Rec_893523,Human_Splice_Rec_893527,Human_Splice_Rec_893531,Human_Splice_Rec_893533 Human_miRNA_ID_1913995,Human_miRNA_ID_1916446,Human_miRNA_ID_1918895,Human_miRNA_ID_1921352,Human_miRNA_ID_1923810,Human_miRNA_ID_1926260,Human_miRNA_ID_1928712,Human_miRNA_ID_1931164,Human_miRNA_ID_2628993,Human_miRNA_ID_2642102,Human_miRNA_ID_3124845 RMVar_hsa_circ_95022,RMVar_hsa_circ_246779 74358 RMVar_ID_74358 Human_SNP_ID_332086496 m1A Human chr7 + 98281926 98281926 98281926 CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTACCTCGTCACAGGTGGGCCCGTAACCAACTTTC CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTGCCTCGTCACAGGTGGGCCCGTAACCAACTTTC A G BRI3 Ensembl:ENSG00000164713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:98281876..98281950 26863196 MeRIP-seq:(Medium) rs1469279706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17427020 Human_Splice_Rec_893523,Human_Splice_Rec_893527,Human_Splice_Rec_893531,Human_Splice_Rec_893533 Human_miRNA_ID_1913995,Human_miRNA_ID_1916446,Human_miRNA_ID_1918895,Human_miRNA_ID_1921352,Human_miRNA_ID_1923810,Human_miRNA_ID_1926260,Human_miRNA_ID_1928712,Human_miRNA_ID_1931164,Human_miRNA_ID_2628993,Human_miRNA_ID_2642102,Human_miRNA_ID_3124845 RMVar_hsa_circ_95022,RMVar_hsa_circ_246779 74359 RMVar_ID_74359 Human_SNP_ID_332088213 m1A Human chr7 - 98287586 98287586 98287586 ACTCCCACTGCCACGGGCCAGGGCGCCGGCCCACCTGAGTGCTAGGATTTCCAGCAGCGCCAGCC ACTCCCACTGCCACGGGCCAGGGCGCCGGCCCCCCTGAGTGCTAGGATTTCCAGCAGCGCCAGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:98287577..98287701 26863196 MeRIP-seq:(Medium) rs903502398 Functional Loss SNV dbSNP153 33..33 33 - - - 74360 RMVar_ID_74360 Human_SNP_ID_332089514 m1A Human chr7 + 98291213 98291213 98291213 TTCATTTGCTGTTTTGCCTTGAGGAAGCGACGATGCCCCAACTGTGGAGCCACCTTCGCTTAAAG TTCATTTGCTGTTTTGCCTTGAGGAAGCGACGGTGCCCCAACTGTGGAGCCACCTTCGCTTAAAG A G BRI3 Ensembl:ENSG00000164713 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:98283002..98291325 32194978 MeRIP-seq:(Medium) rs774581185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690750,Human_RBP_ID_1690112,Human_RBP_ID_2049829,Human_RBP_ID_3859204,Human_RBP_ID_9215576,Human_RBP_ID_16260383,Human_RBP_ID_17542974,Human_RBP_ID_26830517,Human_RBP_ID_27534322 RMVar_hsa_circ_123304,RMVar_hsa_circ_95022,RMVar_hsa_circ_246779,RMVar_hsa_circ_246781,RMVar_hsa_circ_120521,RMVar_hsa_circ_246782 74361 RMVar_ID_74361 Human_SNP_ID_332095315 m1A Human chr7 + 98310568 98310568 98310568 AGGAGCGGGGGGCATCTTTGGTGAGCATTTAGAAAGGGTGTCGTAATCTTTCCTAACCTGTGAAA AGGAGCGGGGGGCATCTTTGGTGAGCATTTAGCAAGGGTGTCGTAATCTTTCCTAACCTGTGAAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:98310517..98310624 26863196 MeRIP-seq:(Medium) rs768819567 Functional Loss SNV dbSNP153 33..33 33 - - - 74362 RMVar_ID_74362 Human_SNP_ID_332097371 m1A Human chr7 - 98317933 98317933 98317933 GTGTGAAATGAGTGAGGGCCCCGGCCAGTGTGAGGATGATGTGAACTGTGGGGTGAGGGTCCCAG GTGTGAAATGAGTGAGGGCCCCGGCCAGTGTGTGGATGATGTGAACTGTGGGGTGAGGGTCCCAG T A BAIAP2L1 Ensembl:ENSG00000006453 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:98317924..98318113 26863196 MeRIP-seq:(Medium) rs1381584434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90201,RMVar_hsa_circ_101627,RMVar_hsa_circ_87367,RMVar_hsa_circ_246784,RMVar_hsa_circ_246783,RMVar_hsa_circ_359198,RMVar_hsa_circ_107450,RMVar_hsa_circ_350486,RMVar_hsa_circ_102476,RMVar_hsa_circ_246790,RMVar_hsa_circ_246792,RMVar_hsa_circ_246793,RMVar_hsa_circ_246791,RMVar_hsa_circ_72488,RMVar_hsa_circ_34302,RMVar_hsa_circ_350704,RMVar_hsa_circ_60267,RMVar_hsa_circ_61961,RMVar_hsa_circ_20691 74363 RMVar_ID_74363 Human_SNP_ID_332116123 m1A Human chr7 - 98386525 98386525 98386525 ACGAAAGGCGGCAAAAAGGGAGCCAAGAAGAAAGTGGTTGATCCATTTTCTAAGAAAGATTGGTA ACGAAAGGCGGCAAAAAGGGAGCCAAGAAGAAGGTGGTTGATCCATTTTCTAAGAAAGATTGGTA T C RPS3AP26,BAIAP2L1 Ensembl:ENSG00000214389,Ensembl:ENSG00000006453 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1454355730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90201,RMVar_hsa_circ_246783,RMVar_hsa_circ_102476,RMVar_hsa_circ_246793 74364 RMVar_ID_74364 Human_SNP_ID_332120553 m1A Human chr7 + 98400987 98400985 98400987 GAGGGTCGGCCGCCGCCGCAGCCGTCGGCCCGAGAGTGCCCGCGCGCGTCTCCGCTGCGAAAATG GAGGGTCGGCCGCCGCCGCAGCCGTCGGCCC__GAGTGCCCGCGCGCGTCTCCGCTGCGAAAATG CGA C RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:98400936..98401055 26863196 MeRIP-seq:(Medium) rs1284658675 Functional Loss DEL dbSNP153 32..33 33 - - - 74365 RMVar_ID_74365 Human_SNP_ID_332245386 m1A Human chr7 + 98878569 98878556 98878569 GGGGCGGGACTGCGCGCGGCCGAGCGGTTGCGACGAGGGCTCGGCTGGGGGTCGCCGGGGTCGCG GGGGCGGGACTGCGCGCGGC_____________CGAGGGCTCGGCTGGGGGTCGCCGGGGTCGCG CCGAGCGGTTGCGA C TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:98878543..98878704 26863196 MeRIP-seq:(Medium) rs1348546858 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_954623,Human_RBP_ID_4953305,Human_RBP_ID_5533905,Human_RBP_ID_8914461,Human_RBP_ID_9337236,Human_RBP_ID_9354768,Human_RBP_ID_18426055,Human_RBP_ID_18452000,Human_RBP_ID_22111837,Human_RBP_ID_27829548 Human_Splice_Rec_893689,Human_Splice_Rec_893831,Human_Splice_Rec_893971 Human_miRNA_ID_2468714,Human_miRNA_ID_2937327 RMVar_hsa_circ_246795,RMVar_hsa_circ_92891 74366 RMVar_ID_74366 Human_SNP_ID_332252247 m1A Human chr7 - 98903509 98903509 98903509 CAAGACAAGACAGGCTGGACGTACGGTTTCTCAGCTCTGTGGTGAGGATGTGTTTGGCAGCAATC CAAGACAAGACAGGCTGGACGTACGGTTTCTCGGCTCTGTGGTGAGGATGTGTTTGGCAGCAATC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:98903487..98903613 26863196 MeRIP-seq:(Medium) rs782677796 Functional Loss SNV dbSNP153 33..33 33 - - - 74367 RMVar_ID_74367 Human_SNP_ID_332252995 m1A Human chr7 + 98906246 98906246 98906246 CATACTAATTGGCTCAGGATATACTGCCAGAGAGACTCTAAGGTATGAGATTAAACCAGTGATAT CATACTAATTGGCTCAGGATATACTGCCAGAGGGACTCTAAGGTATGAGATTAAACCAGTGATAT A G TRRAP Ensembl:ENSG00000196367 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:98906176..98906346 26863196 MeRIP-seq:(Medium) rs781979132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952601,Human_RBP_ID_16261806,Human_RBP_ID_19136817 Human_Splice_Rec_893712,Human_Splice_Rec_893713,Human_Splice_Rec_893854,Human_Splice_Rec_893855,Human_Splice_Rec_893994,Human_Splice_Rec_893995,Human_Splice_Rec_894132,Human_Splice_Rec_894133,Human_Splice_Rec_894252,Human_Splice_Rec_894253 RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_246795,RMVar_hsa_circ_92891,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_82609,RMVar_hsa_circ_25430,RMVar_hsa_circ_15404,RMVar_hsa_circ_246799,RMVar_hsa_circ_246800,RMVar_hsa_circ_101073,RMVar_hsa_circ_95390,RMVar_hsa_circ_246804,RMVar_hsa_circ_98787,RMVar_hsa_circ_246807,RMVar_hsa_circ_89807,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_95025,RMVar_hsa_circ_97292,RMVar_hsa_circ_106318,RMVar_hsa_circ_246811,RMVar_hsa_circ_318773,RMVar_hsa_circ_293355,RMVar_hsa_circ_246814,RMVar_hsa_circ_246815,RMVar_hsa_circ_246816,RMVar_hsa_circ_81669,RMVar_hsa_circ_126943,RMVar_hsa_circ_246817,RMVar_hsa_circ_111045,RMVar_hsa_circ_91293,RMVar_hsa_circ_246819,RMVar_hsa_circ_246821,RMVar_hsa_circ_91964,RMVar_hsa_circ_246820,RMVar_hsa_circ_322031,RMVar_hsa_circ_246818,RMVar_hsa_circ_296638,RMVar_hsa_circ_63536,RMVar_hsa_circ_246822,RMVar_hsa_circ_246823,RMVar_hsa_circ_299203,RMVar_hsa_circ_246824 74368 RMVar_ID_74368 Human_SNP_ID_332252999 m1A Human chr7 - 98906252 98906252 98906252 AACCAGATATCACTGGTTTAATCTCATACCTTAGAGTCTCTCTGGCAGTATATCCTGAGCCAATT AACCAGATATCACTGGTTTAATCTCATACCTTGGAGTCTCTCTGGCAGTATATCCTGAGCCAATT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:98906201..98906371 26863196 MeRIP-seq:(Medium) rs1554407505 Functional Loss SNV dbSNP153 33..33 33 - - - 74369 RMVar_ID_74369 Human_SNP_ID_332276992 m1A Human chr7 - 98995274 98995274 98995274 ACTGGCTCACTAACACCATCTCCCACCATCCCACCTGGTGCCATCTCCTACCGGCTCACCCGGCC ACTGGCTCACTAACACCATCTCCCACCATCCCGCCTGGTGCCATCTCCTACCGGCTCACCCGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:98995244..98995311 26863196 MeRIP-seq:(Medium) rs1000225125 Functional Loss SNV dbSNP153 33..33 33 - - - 74370 RMVar_ID_74370 Human_SNP_ID_332276995 m1A Human chr7 - 98995282 98995282 98995282 TGTCTCCTACTGGCTCACTAACACCATCTCCCACCATCCCACCTGGTGCCATCTCCTACCGGCTC TGTCTCCTACTGGCTCACTAACACCATCTCCCGCCATCCCACCTGGTGCCATCTCCTACCGGCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:98995232..98995412 26863196 MeRIP-seq:(Medium) rs1266400111 Functional Loss SNV dbSNP153 33..33 33 - - - 74371 RMVar_ID_74371 Human_SNP_ID_332313687 m1A Human chr7 - 99142847 99142847 99142847 CCTCCTGGCCTTGCCTCTGTTCCCCTGGTCCCATCCCTCACTTCTCACCACTTTCCCATCATCTC CCTCCTGGCCTTGCCTCTGTTCCCCTGGTCCCCTCCCTCACTTCTCACCACTTTCCCATCATCTC T G SMURF1 Ensembl:ENSG00000198742 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99142845..99142952 26863196 MeRIP-seq:(Medium) rs1448062399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134576,Human_RBP_ID_17093334,Human_RBP_ID_18959428,Human_RBP_ID_21554401 74372 RMVar_ID_74372 Human_SNP_ID_332313958 m1A Human chr7 + 99143593 99143589 99143593 GGGCGGGGCCAGGAGGGAGAAGCGAGGGGCGCACGCCGAAGGGGGTGACGAGGTCCTGGGACAAC GGGCGGGGCCAGGAGGGAGAAGCGAGGGG____CGCCGAAGGGGGTGACGAGGTCCTGGGACAAC GCGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:99143590..99143702 26863196 MeRIP-seq:(Medium) rs1381390617 Functional Loss DEL dbSNP153 30..33 33 - - - 74373 RMVar_ID_74373 Human_SNP_ID_332314173 m1A Human chr7 + 99144052 99144043 99144052 CCGCCGCCTCCGCCGCCGCCTCCGCCGCCTCCACCACCTCAGAGCCGGACGCCCGCCGCCCTCGC CCGCCGCCTCCGCCGCCGCCTCCG_________CCACCTCAGAGCCGGACGCCCGCCGCCCTCGC GCCGCCTCCA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:99143950..99144100 26863410 MeRIP-seq:(Medium) rs896522102 Functional Loss DEL dbSNP153 25..33 33 - - - 74374 RMVar_ID_74374 Human_SNP_ID_332314179 m1A Human chr7 + 99144055 99144055 99144055 CCGCCTCCGCCGCCGCCTCCGCCGCCTCCACCACCTCAGAGCCGGACGCCCGCCGCCCTCGCCGC CCGCCTCCGCCGCCGCCTCCGCCGCCTCCACCGCCTCAGAGCCGGACGCCCGCCGCCCTCGCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:99143773..99144141;chr7:99143690..99144141;chr7:99143695..99144150 26863196 MeRIP-seq:(Medium) rs898497750 Functional Loss SNV dbSNP153 33..33 33 - - - 74375 RMVar_ID_74375 Human_SNP_ID_332371238 m1A Human chr7 + 99363601 99363601 99363601 AGCAAGATTGTCGCAAATTTTGCACTACTGGCATCGATGGAGCCATGACAATTTGGGATTTCAAG AGCAAGATTGTCGCAAATTTTGCACTACTGGCGTCGATGGAGCCATGACAATTTGGGATTTCAAG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99363551..99363625 32194978 MeRIP-seq:(Medium) rs763882333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690932,Human_RBP_ID_2050053,Human_RBP_ID_8219005,Human_RBP_ID_9215667,Human_RBP_ID_16265100,Human_RBP_ID_17314246,Human_RBP_ID_17426707,Human_RBP_ID_17543012,Human_RBP_ID_18385480,Human_RBP_ID_24234181 Human_Splice_Rec_894772,Human_Splice_Rec_894773,Human_Splice_Rec_894794,Human_Splice_Rec_894795,Human_Splice_Rec_894812,Human_Splice_Rec_894813,Human_Splice_Rec_894824,Human_Splice_Rec_894825,Human_Splice_Rec_894827 RMVar_hsa_circ_15222,RMVar_hsa_circ_90807,RMVar_hsa_circ_28226,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_40794,RMVar_hsa_circ_246923,RMVar_hsa_circ_40411,RMVar_hsa_circ_246928,RMVar_hsa_circ_327479 74376 RMVar_ID_74376 Human_SNP_ID_332374165 m1A Human chr7 + 99374757 99374757 99374757 AGCCCAGAGCCGGTTCGGCGCGTCGACTGCCCAGAGTCCGCGGCCGGGGCGCGGGAGGTGAGGGC AGCCCAGAGCCGGTTCGGCGCGTCGACTGCCCGGAGTCCGCGGCCGGGGCGCGGGAGGTGAGGGC A G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:99374701..99376493;chr7:99374701..99374981;chr7:99374701..99374861 26863196 MeRIP-seq:(Medium) rs1462530665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793446,Human_RBP_ID_844021,Human_RBP_ID_4955893,Human_RBP_ID_8915007,Human_RBP_ID_9337239,Human_RBP_ID_18195984,Human_RBP_ID_22620749 Human_Splice_Rec_894853,Human_Splice_Rec_894873,Human_Splice_Rec_894883,Human_Splice_Rec_894903,Human_Splice_Rec_894913,Human_Splice_Rec_894921,Human_Splice_Rec_894929,Human_Splice_Rec_894949,Human_Splice_Rec_894969,Human_Splice_Rec_894989,Human_Splice_Rec_895011,Human_Splice_Rec_895031 Human_miRNA_ID_2423981,Human_miRNA_ID_2423982,Human_miRNA_ID_2433641,Human_miRNA_ID_2433642,Human_miRNA_ID_2783781,Human_miRNA_ID_2783782 RMVar_hsa_circ_90807,RMVar_hsa_circ_5187,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923,RMVar_hsa_circ_106059,RMVar_hsa_circ_246930 74377 RMVar_ID_74377 Human_SNP_ID_332374270 m1A Human chr7 - 99375040 99375040 99375040 CCTGCGGCCACCCCCGCGCCCCCTCCAATCCCAGGGCTCCCTCTCCTTTCCGTGAGCCCCTCGTC CCTGCGGCCACCCCCGCGCCCCCTCCAATCCCCGGGCTCCCTCTCCTTTCCGTGAGCCCCTCGTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99375037..99375446 26863196 MeRIP-seq:(Medium) rs1285305265 Functional Loss SNV dbSNP153 33..33 33 - - - 74378 RMVar_ID_74378 Human_SNP_ID_332377333 m1A Human chr7 + 99385770 99385770 99385770 GGAGCCCATCAGCTGCCACGCCTGGAACAAGGACCGCACCCGTGAGTGCTTGCTGGGGGCCGGTG GGAGCCCATCAGCTGCCACGCCTGGAACAAGGGCCGCACCCGTGAGTGCTTGCTGGGGGCCGGTG A G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99385722..99386413 32194978 MeRIP-seq:(Medium) rs549905620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793448,Human_RBP_ID_844023,Human_RBP_ID_4956489,Human_RBP_ID_9403634,Human_RBP_ID_18195985,Human_RBP_ID_23215565,Human_RBP_ID_26830534 Human_Splice_Rec_894736,Human_Splice_Rec_894737,Human_Splice_Rec_894774,Human_Splice_Rec_894775,Human_Splice_Rec_894830,Human_Splice_Rec_894831,Human_Splice_Rec_894848,Human_Splice_Rec_894849,Human_Splice_Rec_894856,Human_Splice_Rec_894857,Human_Splice_Rec_894874,Human_Splice_Rec_894875,Human_Splice_Rec_894886,Human_Splice_Rec_894887,Human_Splice_Rec_894908,Human_Splice_Rec_894909,Human_Splice_Rec_894918,Human_Splice_Rec_894919,Human_Splice_Rec_894922,Human_Splice_Rec_894923,Human_Splice_Rec_894934,Human_Splice_Rec_894935,Human_Splice_Rec_894952,Human_Splice_Rec_894953,Human_Splice_Rec_894972,Human_Splice_Rec_894973,Human_Splice_Rec_894994,Human_Splice_Rec_894995,Human_Splice_Rec_895014,Human_Splice_Rec_895015,Human_Splice_Rec_895032,Human_Splice_Rec_895033,Human_Splice_Rec_895049,Human_Splice_Rec_895055,Human_Splice_Rec_895065 RMVar_hsa_circ_90807,RMVar_hsa_circ_5187,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923,RMVar_hsa_circ_106059,RMVar_hsa_circ_246930,RMVar_hsa_circ_19961,RMVar_hsa_circ_291657,RMVar_hsa_circ_341829,RMVar_hsa_circ_375343,RMVar_hsa_circ_336841,RMVar_hsa_circ_111360,RMVar_hsa_circ_246932,RMVar_hsa_circ_246933,RMVar_hsa_circ_246934,RMVar_hsa_circ_246931 74379 RMVar_ID_74379 Human_SNP_ID_332378059 m1A Human chr7 + 99388092 99388078 99388093 GTAACCGTATTGTGACCTGCGGCACAGACCGCAACGCCTACGTGTGGACGCTGAAGGGCCGCACA GTAACCGTATTGTGACCTG_______________CGCCTACGTGTGGACGCTGAAGGGCCGCACA GCGGCACAGACCGCAA G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:99387989..99388279 26863196 MeRIP-seq:(Medium) rs1208291521 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_174692,Human_RBP_ID_3972163,Human_RBP_ID_9311365,Human_RBP_ID_9337241,Human_RBP_ID_19021114,Human_RBP_ID_24234224,Human_RBP_ID_26830542 Human_Splice_Rec_894740,Human_Splice_Rec_894778,Human_Splice_Rec_894834,Human_Splice_Rec_894852,Human_Splice_Rec_894860,Human_Splice_Rec_894878,Human_Splice_Rec_894890,Human_Splice_Rec_894912,Human_Splice_Rec_894926,Human_Splice_Rec_894938,Human_Splice_Rec_894956,Human_Splice_Rec_894976,Human_Splice_Rec_894998,Human_Splice_Rec_895018,Human_Splice_Rec_895036,Human_Splice_Rec_895052,Human_Splice_Rec_895060,Human_Splice_Rec_895068,Human_Splice_Rec_895078 RMVar_hsa_circ_246938,RMVar_hsa_circ_5187,RMVar_hsa_circ_98173,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923,RMVar_hsa_circ_106059,RMVar_hsa_circ_246930,RMVar_hsa_circ_43744,RMVar_hsa_circ_19961,RMVar_hsa_circ_341829,RMVar_hsa_circ_375343,RMVar_hsa_circ_336841,RMVar_hsa_circ_111360,RMVar_hsa_circ_246932,RMVar_hsa_circ_246933,RMVar_hsa_circ_246934,RMVar_hsa_circ_277562,RMVar_hsa_circ_272808,RMVar_hsa_circ_112726,RMVar_hsa_circ_246935,RMVar_hsa_circ_246936,RMVar_hsa_circ_274968,RMVar_hsa_circ_287166,RMVar_hsa_circ_373763,RMVar_hsa_circ_122850,RMVar_hsa_circ_246940,RMVar_hsa_circ_246942,RMVar_hsa_circ_105609,RMVar_hsa_circ_246941,RMVar_hsa_circ_246939,RMVar_hsa_circ_246937 74380 RMVar_ID_74380 Human_SNP_ID_332379373 m1A Human chr7 - 99392584 99392584 99392584 GGGAAGGCCAGGCGGGCGTCTGGCCGCCCGGGAGGCAGATGCCAGCTCAAGGATACAGACGGGCC GGGAAGGCCAGGCGGGCGTCTGGCCGCCCGGGGGGCAGATGCCAGCTCAAGGATACAGACGGGCC T C PDAP1 Ensembl:ENSG00000106244 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:99392554..99392698 26863196 MeRIP-seq:(Medium) rs781438023 Functional Loss SNV dbSNP153 33..33 33 - - - 74381 RMVar_ID_74381 Human_SNP_ID_332380777 m1A Human chr7 - 99396587 99396587 99396587 TCGCCCACCCTGTGCCCTGGCGCCGCTGCAACAGCCCCTCATGGCCAGGAGCCCCCCATGGCCTG TCGCCCACCCTGTGCCCTGGCGCCGCTGCAACGGCCCCTCATGGCCAGGAGCCCCCCATGGCCTG T C PDAP1 Ensembl:ENSG00000106244 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:99396536..99396700 26863196 MeRIP-seq:(Medium) rs1046863534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_690996,Human_RBP_ID_4954002,Human_RBP_ID_8675293 74382 RMVar_ID_74382 Human_SNP_ID_332382724 m1A Human chr7 + 99403557 99403557 99403557 CCTGCAGAATCAAAAATGCAAAACAAATCCCCAAGACTGTGACCCTATCACCCCCCAGACTGTGG CCTGCAGAATCAAAAATGCAAAACAAATCCCCCAGACTGTGACCCTATCACCCCCCAGACTGTGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:99403554..99403672 32194978 MeRIP-seq:(Medium) rs1451479504 Functional Loss SNV dbSNP153 33..33 33 - - - 74383 RMVar_ID_74383 Human_SNP_ID_332382725 m1A Human chr7 + 99403557 99403557 99403557 CCTGCAGAATCAAAAATGCAAAACAAATCCCCAAGACTGTGACCCTATCACCCCCCAGACTGTGG CCTGCAGAATCAAAAATGCAAAACAAATCCCCTAGACTGTGACCCTATCACCCCCCAGACTGTGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:99403554..99403672 32194978 MeRIP-seq:(Medium) rs1451479504 Functional Loss SNV dbSNP153 33..33 33 - - - 74384 RMVar_ID_74384 Human_SNP_ID_332384067 m1A Human chr7 - 99408836 99408836 99408836 TGCCTGTATAGAATTCCAGAGCCGCTGTTGCCATTTGCCCTCACTTCCGGTGGGTGGCAGGCAGG TGCCTGTATAGAATTCCAGAGCCGCTGTTGCCGTTTGCCCTCACTTCCGGTGGGTGGCAGGCAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99408788..99408888 32194978 MeRIP-seq:(Medium) rs1160924678 Functional Loss SNV dbSNP153 33..33 33 - - - 74385 RMVar_ID_74385 Human_SNP_ID_332387268 m1A Human chr7 - 99419453 99419453 99419453 CAGGAACCTGCGAAGTCCAGAGTCCAGGGTGGAGCGCGCCAGCCTCAGCCAGAGCAGCCACGACA CAGGAACCTGCGAAGTCCAGAGTCCAGGGTGGGGCGCGCCAGCCTCAGCCAGAGCAGCCACGACA T C PTCD1 Ensembl:ENSG00000106246 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:99419324..99419500 26863196 MeRIP-seq:(Medium) rs1284096607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8913858 74386 RMVar_ID_74386 Human_SNP_ID_332391720 m1A Human chr7 + 99432945 99432945 99432945 GTGCTACACACCTGTGCTCACAGCTACTGGCGAGGCTGAGGCAGGAGGAACTCTTGAGCCAAGGA GTGCTACACACCTGTGCTCACAGCTACTGGCGGGGCTGAGGCAGGAGGAACTCTTGAGCCAAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:99432943..99433373 32194978 MeRIP-seq:(Medium) rs755867036 Functional Loss SNV dbSNP153 33..33 33 - - - 74387 RMVar_ID_74387 Human_SNP_ID_332393626 m1A Human chr7 - 99439020 99439020 99439020 CCCCCTCGGTCTCCTGCAGCCTTCTCGCCTTTACCCGCCGCCGGCCCCGCCGCACACACTCCTCC CCCCCTCGGTCTCCTGCAGCCTTCTCGCCTTTCCCCGCCGCCGGCCCCGCCGCACACACTCCTCC T G PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:99438904..99439200;chr7:99438885..99439221;chr7:99438881..99439237 26863196 MeRIP-seq:(Medium) rs894310827 Functional Loss SNV dbSNP153 33..33 33 - - - 74388 RMVar_ID_74388 Human_SNP_ID_332395497 m1A Human chr7 - 99444780 99444779 99444780 ATTCACAGACAGCAGCGCCCGACTCTGTAGAAAGGAGAGAAAAGGAGAGGAATCAAAGAGGTGCA ATTCACAGACAGCAGCGCCCGACTCTGTAGAA_GGAGAGAAAAGGAGAGGAATCAAAGAGGTGCA CT C PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99444776..99444850 26863196 MeRIP-seq:(Medium) rs768278236 Functional Loss DEL dbSNP153 33..33 33 - - - 74389 RMVar_ID_74389 Human_SNP_ID_332395508 m1A Human chr7 - 99444806 99444805 99444807 TTTGCCGCAGGCAGCTTTCAAAAAGAATTCACAGACAGCAGCGCCCGACTCTGTAGAAAGGAGAG TTTGCCGCAGGCAGCTTTCAAAAAGAATTCA__GACAGCAGCGCCCGACTCTGTAGAAAGGAGAG CTG C PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:99444776..99444850 26863196 MeRIP-seq:(Medium) rs1472070192 Functional Loss DEL dbSNP153 32..33 33 - - - 74390 RMVar_ID_74390 Human_SNP_ID_332399167 m1A Human chr7 - 99458357 99458357 99458357 TAAGATACTTACCATCTTGCCTTCCTGACTTCAGAGCACGAGCGGCTCCGCAAATACCACTGAAG TAAGATACTTACCATCTTGCCTTCCTGACTTCGGAGCACGAGCGGCTCCGCAAATACCACTGAAG T C PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99458251..99458375 32194978 MeRIP-seq:(Medium) rs1206467254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3119770,Human_RBP_ID_19136894,Human_RBP_ID_21551700,Human_RBP_ID_22464125,Human_RBP_ID_26128364 RMVar_hsa_circ_56746,RMVar_hsa_circ_331959 74391 RMVar_ID_74391 Human_SNP_ID_332399466 m1A Human chr7 - 99459265 99459265 99459265 CCAGCAGGGCAGTGAGCGCCTCTTGCGTTTGCAGGTTACTACCGGTACTACAACAAGTACATCAA CCAGCAGGGCAGTGAGCGCCTCTTGCGTTTGCGGGTTACTACCGGTACTACAACAAGTACATCAA T C PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr7:99459096..99459317;chr7:99459126..99459275 26863196,32194978 MeRIP-seq:(Medium) rs1203670563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17314701,Human_RBP_ID_17665377,Human_RBP_ID_22463199,Human_RBP_ID_22774404 RMVar_hsa_circ_358274,RMVar_hsa_circ_331959,RMVar_hsa_circ_246956 74392 RMVar_ID_74392 Human_SNP_ID_332399712 m1A Human chr7 - 99460195 99460195 99460195 TCAGTGGGTATTTTTTCTCACTCTTCCGTTTCAGTACCAGTGAAGGACAAGAAACTTCTGGAGGT TCAGTGGGTATTTTTTCTCACTCTTCCGTTTCTGTACCAGTGAAGGACAAGAAACTTCTGGAGGT T A PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99448156..99466175 26863196 MeRIP-seq:(Medium) rs760970218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86876,Human_RBP_ID_3119783,Human_RBP_ID_9403651,Human_RBP_ID_16266477,Human_RBP_ID_22464600,Human_RBP_ID_22555237,Human_RBP_ID_26128372 Human_Splice_Rec_895362 74393 RMVar_ID_74393 Human_SNP_ID_332401227 m1A Human chr7 - 99466041 99466041 99466041 AGGGTCCAGGGTCCAGAGCCACACTGGGAGAGAAGGAAGCTGCGGAGCTGCCTGCCCTTTGCTCA AGGGTCCAGGGTCCAGAGCCACACTGGGAGAGGAGGAAGCTGCGGAGCTGCCTGCCCTTTGCTCA T C PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:99466038..99466175 26863196 MeRIP-seq:(Medium) rs889607265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5401606,Human_RBP_ID_16266713,Human_RBP_ID_19135175,Human_RBP_ID_23080668 74394 RMVar_ID_74394 Human_SNP_ID_332403304 m1A Human chr7 - 99472932 99472932 99472932 TCCGCGCCCCTCGGCGAATCACCCCTTACCGGAGGAACAGACACAACCACTCTGGCAGCCTCAGA TCCGCGCCCCTCGGCGAATCACCCCTTACCGGCGGAACAGACACAACCACTCTGGCAGCCTCAGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:99472882..99473340 26863196 MeRIP-seq:(Medium) rs1482014805 Functional Loss SNV dbSNP153 33..33 33 - - - 74395 RMVar_ID_74395 Human_SNP_ID_332412259 m1A Human chr7 - 99505031 99505031 99505031 CCGCTCGCACAGCATCACCAAAGCGGGGAGGCAAACGGAGCCACTCTCTCCCCTGCTCCATCCCA CCGCTCGCACAGCATCACCAAAGCGGGGAGGCCAACGGAGCCACTCTCTCCCCTGCTCCATCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99505015..99505140 26863196 MeRIP-seq:(Medium) rs1422742132 Functional Loss SNV dbSNP153 33..33 33 - - - 74396 RMVar_ID_74396 Human_SNP_ID_332426205 m1A Human chr7 + 99558053 99558053 99558053 TGCATAGATTTTAGTCTTCCCACCAGGGACGCAACTGTCAGTTTCCTCCGTCTCTCTCGGTTCTA TGCATAGATTTTAGTCTTCCCACCAGGGACGCCACTGTCAGTTTCCTCCGTCTCTCTCGGTTCTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:99558002..99558231 26863196 MeRIP-seq:(Medium) rs1292495484 Functional Loss SNV dbSNP153 33..33 33 - - - 74397 RMVar_ID_74397 Human_SNP_ID_332426451 m1A Human chr7 + 99558762 99558762 99558762 GGCCCCGAGCGCGAGTGTGTAGGTGACAGGACAGCGGCCAGGCCCGCCCCTCCCCTCGGTGAGTA GGCCCCGAGCGCGAGTGTGTAGGTGACAGGACCGCGGCCAGGCCCGCCCCTCCCCTCGGTGAGTA A C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr7:99558665..99560581;chr7:99558681..99558770;chr7:99558620..99560550 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1044473533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955895,Human_RBP_ID_8915012,Human_RBP_ID_18426060 Human_Splice_Rec_895553,Human_Splice_Rec_895561,Human_Splice_Rec_895565,Human_Splice_Rec_895571,Human_Splice_Rec_895577,Human_Splice_Rec_895579,Human_Splice_Rec_895583,Human_Splice_Rec_895593,Human_Splice_Rec_895599,Human_Splice_Rec_895607,Human_Splice_Rec_895611,Human_Splice_Rec_895621,Human_Splice_Rec_895629,Human_Splice_Rec_895633,Human_Splice_Rec_895641,Human_Splice_Rec_895647,Human_Splice_Rec_895695 74398 RMVar_ID_74398 Human_SNP_ID_332506788 m1A Human chr7 - 99903592 99903592 99903592 TGCTTATGTCTTCCTTCTTTTCACAGAATCCAAAAGAAGTGTTGACCAGGTATGCACTCCTGTTC TGCTTATGTCTTCCTTCTTTTCACAGAATCCAGAAGAAGTGTTGACCAGGTATGCACTCCTGTTC T C TRIM4 Ensembl:ENSG00000146833 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99903223..99908281 32194978 MeRIP-seq:(Medium) rs1482412964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953275,Human_RBP_ID_5402236,Human_RBP_ID_22620787,Human_RBP_ID_22685631,Human_RBP_ID_26356761 Human_Splice_Rec_896508,Human_Splice_Rec_896509,Human_Splice_Rec_896520,Human_Splice_Rec_896521,Human_Splice_Rec_896530,Human_Splice_Rec_896531,Human_Splice_Rec_896540,Human_Splice_Rec_896541 RMVar_hsa_circ_53643,RMVar_hsa_circ_109179,RMVar_hsa_circ_307564,RMVar_hsa_circ_246980,RMVar_hsa_circ_331143,RMVar_hsa_circ_68525,RMVar_hsa_circ_246981,RMVar_hsa_circ_246982,RMVar_hsa_circ_246983,RMVar_hsa_circ_86239 74399 RMVar_ID_74399 Human_SNP_ID_332535314 m1A Human chr7 - 100015687 100015687 100015687 CCCGGGAGCGGCCTGGGGGCGCTGGGCGAGAAAGGGGAGCTGACTCTGGGGCTCAGGCCGGCCGA CCCGGGAGCGGCCTGGGGGCGCTGGGCGAGAATGGGGAGCTGACTCTGGGGCTCAGGCCGGCCGA T A RF00017-6474 RNACentral:URS000097CF0E SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100015636..100015725 26863196 MeRIP-seq:(Medium) rs748020634 Functional Loss SNV dbSNP153 33..33 33 - - - 74400 RMVar_ID_74400 Human_SNP_ID_332535318 m1A Human chr7 - 100015713 100015713 100015713 GGCCGGCCCCAAGTCTCACCGTGAGCCCCGGGAGCGGCCTGGGGGCGCTGGGCGAGAAAGGGGAG GGCCGGCCCCAAGTCTCACCGTGAGCCCCGGGGGCGGCCTGGGGGCGCTGGGCGAGAAAGGGGAG T C RF00017-6474 RNACentral:URS000097CF0E SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:100015601..100015750 26863196 MeRIP-seq:(Medium) rs1250191603 Functional Loss SNV dbSNP153 33..33 33 - - - 74401 RMVar_ID_74401 Human_SNP_ID_332536483 m1A Human chr7 + 100020231 100020231 100020231 GATTTGAAAAGGCAGAGAGGACTGCGGGGGGAAGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG GATTTGAAAAGGCAGAGAGGACTGCGGGGGGACGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG A C ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100020227..100020327 26863196 MeRIP-seq:(Medium) rs975011395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7777732 RMVar_hsa_circ_97244,RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_93542,RMVar_hsa_circ_246986,RMVar_hsa_circ_246988 74402 RMVar_ID_74402 Human_SNP_ID_332536484 m1A Human chr7 + 100020231 100020231 100020231 GATTTGAAAAGGCAGAGAGGACTGCGGGGGGAAGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG GATTTGAAAAGGCAGAGAGGACTGCGGGGGGAGGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100020227..100020327 26863196 MeRIP-seq:(Medium) rs975011395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7777732 RMVar_hsa_circ_97244,RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_93542,RMVar_hsa_circ_246986,RMVar_hsa_circ_246988 74403 RMVar_ID_74403 Human_SNP_ID_332536485 m1A Human chr7 + 100020231 100020231 100020231 GATTTGAAAAGGCAGAGAGGACTGCGGGGGGAAGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG GATTTGAAAAGGCAGAGAGGACTGCGGGGGGATGTCCCAGGCATGGAGTGTGATGTGAGGAAAGG A T ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100020227..100020327 26863196 MeRIP-seq:(Medium) rs975011395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7777732 RMVar_hsa_circ_97244,RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_93542,RMVar_hsa_circ_246986,RMVar_hsa_circ_246988 74404 RMVar_ID_74404 Human_SNP_ID_332540040 m1A Human chr7 + 100033417 100033417 100033417 ACAGGAAGATCCCAGAAAGAGTTTGGAGAGAAACGTGACCAGGAGGGCAAAACAGGAGAAAGACA ACAGGAAGATCCCAGAAAGAGTTTGGAGAGAAGCGTGACCAGGAGGGCAAAACAGGAGAAAGACA A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100033366..100033539 26863196 MeRIP-seq:(Medium) rs1386831698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83825,Human_RBP_ID_843916,Human_RBP_ID_3972169,Human_RBP_ID_7777781,Human_RBP_ID_8913929,Human_RBP_ID_24549131,Human_RBP_ID_26356769 RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_86452,RMVar_hsa_circ_246994,RMVar_hsa_circ_246996 74405 RMVar_ID_74405 Human_SNP_ID_332540043 m1A Human chr7 + 100033422 100033422 100033422 AAGATCCCAGAAAGAGTTTGGAGAGAAACGTGACCAGGAGGGCAAAACAGGAGAAAGACAGCAGA AAGATCCCAGAAAGAGTTTGGAGAGAAACGTGTCCAGGAGGGCAAAACAGGAGAAAGACAGCAGA A T ZKSCAN1 Ensembl:ENSG00000106261 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100033372..100033523 26863196 MeRIP-seq:(Medium) rs547956539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83825,Human_RBP_ID_843916,Human_RBP_ID_3972169,Human_RBP_ID_5533607,Human_RBP_ID_7777781,Human_RBP_ID_22111862,Human_RBP_ID_24549131,Human_RBP_ID_26356769 RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_86452,RMVar_hsa_circ_246994,RMVar_hsa_circ_246996 74406 RMVar_ID_74406 Human_SNP_ID_332544277 m1A Human chr7 - 100049843 100049843 100049843 GTCCGCCTCGCTAACCCGCGACCAGCAGGCTCACCATGAATCAGAGCCGCTCCGGGTACCGGGAG GTCCGCCTCGCTAACCCGCGACCAGCAGGCTCGCCATGAATCAGAGCCGCTCCGGGTACCGGGAG T C RF00017-6474 RNACentral:URS000097CF0E SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100049792..100049902;chr7:100049802..100049943;chr7:100049810..100049927 26863196 MeRIP-seq:(Medium) rs1046445426 Functional Loss SNV dbSNP153 33..33 33 - - - 74407 RMVar_ID_74407 Human_SNP_ID_332544889 m1A Human chr7 + 100051582 100051582 100051582 CTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACGGCGCCGGGCCCCCTAGGGATTTTCAGGTAC CTCCCAAAGTGCTGGAATTACAGGTGTGAGCCGCGGCGCCGGGCCCCCTAGGGATTTTCAGGTAC A G ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100051507..100051648 26863196 MeRIP-seq:(Medium) rs1158740977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_896649 RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 74408 RMVar_ID_74408 Human_SNP_ID_332545113 m1A Human chr7 + 100052512 100052512 100052512 TGACCCCAGGTTTTTCGGTCCAAGTAAAAAGAACAATGAGAGTTGCCATTAGCTGAGATGAGCAG TGACCCCAGGTTTTTCGGTCCAAGTAAAAAGAGCAATGAGAGTTGCCATTAGCTGAGATGAGCAG A G ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100052509..100052710 26863196 MeRIP-seq:(Medium) rs944037352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16269951 RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 74409 RMVar_ID_74409 Human_SNP_ID_332545122 m1A Human chr7 - 100052549 100052549 100052549 CATGTCCAAAATGGAATTCCCATCTCTCCCTCAAAAGCTGCTCATCTCAGCTAATGGCAACTCTC CATGTCCAAAATGGAATTCCCATCTCTCCCTCGAAAGCTGCTCATCTCAGCTAATGGCAACTCTC T C RF00017-6474 RNACentral:URS000097CF0E SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100052544..100052690 26863196 MeRIP-seq:(Medium) rs1226267825 Functional Loss SNV dbSNP153 33..33 33 - - - 74410 RMVar_ID_74410 Human_SNP_ID_332553309 m1A Human chr7 - 100081686 100081686 100081686 GTCCCCGGTGTGTGGGTCTGTGACAGGGTCCAACAGGGCCTGGTCCGTGTCCGGTCCCCCAAATC GTCCCCGGTGTGTGGGTCTGTGACAGGGTCCAGCAGGGCCTGGTCCGTGTCCGGTCCCCCAAATC T C ZNF3 Ensembl:ENSG00000166526 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:100081572..100081685;chr7:100081615..100081699 26863196 MeRIP-seq:(Medium) rs565512191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794457,Human_RBP_ID_4957323,Human_RBP_ID_18426061 Human_Splice_Rec_896663,Human_Splice_Rec_896673,Human_Splice_Rec_896681,Human_Splice_Rec_896697,Human_Splice_Rec_896703,Human_Splice_Rec_896707,Human_Splice_Rec_896725,Human_Splice_Rec_896739,Human_Splice_Rec_896745,Human_Splice_Rec_896753,Human_Splice_Rec_896759,Human_Splice_Rec_896763 74411 RMVar_ID_74411 Human_SNP_ID_332555431 m1A Human chr7 + 100089838 100089838 100089838 GGGGAAGATGGAGAGGGTTGGAAAGAAACAGGAGAGGAGACCAAGAACAGGGGAGAAAAAGTGAA GGGGAAGATGGAGAGGGTTGGAAAGAAACAGGCGAGGAGACCAAGAACAGGGGAGAAAAAGTGAA A C COPS6 Ensembl:ENSG00000168090 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100089590..100089984 26863196 MeRIP-seq:(Medium) rs1277803456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87488,Human_RBP_ID_5221654,Human_RBP_ID_5402237,Human_RBP_ID_22419042 74412 RMVar_ID_74412 Human_SNP_ID_332555675 m1A Human chr7 + 100090601 100090601 100090601 TGTGCATTGTCCCTCTCTTCCAGGTGTGTGAGATCATCGAGAGCCCCCTCTTTCTGAAGTTGAAC TGTGCATTGTCCCTCTCTTCCAGGTGTGTGAGCTCATCGAGAGCCCCCTCTTTCTGAAGTTGAAC A C COPS6 Ensembl:ENSG00000168090 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100090576..100090625 26863196 MeRIP-seq:(Medium) rs1359812367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691337,Human_RBP_ID_5401610,Human_RBP_ID_8675704,Human_RBP_ID_9403668,Human_RBP_ID_18888612,Human_RBP_ID_22620798,Human_RBP_ID_22687080,Human_RBP_ID_22746692,Human_RBP_ID_26830589 Human_Splice_Rec_896776,Human_Splice_Rec_896777,Human_Splice_Rec_896798,Human_Splice_Rec_896799,Human_Splice_Rec_896818,Human_Splice_Rec_896819,Human_Splice_Rec_896828,Human_Splice_Rec_896829,Human_Splice_Rec_896840,Human_Splice_Rec_896841,Human_Splice_Rec_896852 RMVar_hsa_circ_328321 74413 RMVar_ID_74413 Human_SNP_ID_332555984 m1A Human chr7 - 100091522 100091522 100091522 AAGCCCCGCCTCCCCATCCGGGTTTTACACTCACATCATAAAAATCTGTCTTGAACTTGTCTGTG AAGCCCCGCCTCCCCATCCGGGTTTTACACTCGCATCATAAAAATCTGTCTTGAACTTGTCTGTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100091401..100091658 32194978 MeRIP-seq:(Medium) rs755909532 Functional Loss SNV dbSNP153 33..33 33 - - - 74414 RMVar_ID_74414 Human_SNP_ID_332556132 m1A Human chr7 + 100091827 100091827 100091827 GTACTTGAAGGGCTGATGGACAGGGGTCAGGCAACTATCCCAAAGGGGAGGGCACTACACTTCCT GTACTTGAAGGGCTGATGGACAGGGGTCAGGCCACTATCCCAAAGGGGAGGGCACTACACTTCCT A C COPS6 Ensembl:ENSG00000168090 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100091651..100091954 32194978 MeRIP-seq:(Medium) rs1174527965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691345,Human_RBP_ID_794469,Human_RBP_ID_1053695,Human_RBP_ID_3120283,Human_RBP_ID_5123046,Human_RBP_ID_5152984,Human_RBP_ID_8675710,Human_RBP_ID_17314358,Human_RBP_ID_17426808,Human_RBP_ID_17543117,Human_RBP_ID_17664286,Human_RBP_ID_18107787,Human_RBP_ID_22464608,Human_RBP_ID_23215573 74415 RMVar_ID_74415 Human_SNP_ID_332556660 m1A Human chr7 - 100093128 100093128 100093128 CCTTACACACCCACTCATTTCCTTCAGGACTCAGAGACCAGCAGATGTGATATTTGCCACCGTCC CCTTACACACCCACTCATTTCCTTCAGGACTCGGAGACCAGCAGATGTGATATTTGCCACCGTCC T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100092930..100093173 26863196 MeRIP-seq:(Medium) rs759864688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2050373,Human_RBP_ID_5123414,Human_RBP_ID_9215812,Human_RBP_ID_17664624,Human_RBP_ID_19019888,Human_RBP_ID_22464611,Human_RBP_ID_22620800 Human_Splice_Rec_896882,Human_Splice_Rec_896910,Human_Splice_Rec_896936,Human_Splice_Rec_896962,Human_Splice_Rec_897004 RMVar_hsa_circ_86292,RMVar_hsa_circ_101507,RMVar_hsa_circ_107157,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_125562,RMVar_hsa_circ_111868,RMVar_hsa_circ_106455,RMVar_hsa_circ_92119,RMVar_hsa_circ_96816,RMVar_hsa_circ_91138,RMVar_hsa_circ_247010,RMVar_hsa_circ_247014,RMVar_hsa_circ_247018,RMVar_hsa_circ_76034,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_247015,RMVar_hsa_circ_247012,RMVar_hsa_circ_247013,RMVar_hsa_circ_247011,RMVar_hsa_circ_247009 74416 RMVar_ID_74416 Human_SNP_ID_332557851 m1A Human chr7 - 100095801 100095801 100095801 CTCCCGGTTTGACCTCCTCTGGCTGATTCAGGACCGGCCCGACCGAGACAATGACCTACGGTGAA CTCCCGGTTTGACCTCCTCTGGCTGATTCAGGTCCGGCCCGACCGAGACAATGACCTACGGTGAA T A MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100095751..100095800 26863196 MeRIP-seq:(Medium) rs1175343913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844043,Human_RBP_ID_1690746,Human_RBP_ID_2050385,Human_RBP_ID_3860076,Human_RBP_ID_7778057,Human_RBP_ID_8272049,Human_RBP_ID_8675754,Human_RBP_ID_8914117,Human_RBP_ID_9311071,Human_RBP_ID_16270467,Human_RBP_ID_17314380,Human_RBP_ID_17426823,Human_RBP_ID_18888670,Human_RBP_ID_22463213,Human_RBP_ID_22516400,Human_RBP_ID_22835819,Human_RBP_ID_23079805,Human_RBP_ID_26129372,Human_RBP_ID_27118942,Human_RBP_ID_27361356 Human_Splice_Rec_896875,Human_Splice_Rec_896903,Human_Splice_Rec_896929,Human_Splice_Rec_896955,Human_Splice_Rec_896997,Human_Splice_Rec_897005 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,RMVar_hsa_circ_101507,RMVar_hsa_circ_107157,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_106455,RMVar_hsa_circ_96816,RMVar_hsa_circ_91138,RMVar_hsa_circ_247014,RMVar_hsa_circ_247018,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_247015,RMVar_hsa_circ_247013,RMVar_hsa_circ_49459,RMVar_hsa_circ_46075,RMVar_hsa_circ_104344,RMVar_hsa_circ_341554,RMVar_hsa_circ_373853,RMVar_hsa_circ_107879,RMVar_hsa_circ_247024,RMVar_hsa_circ_247026,RMVar_hsa_circ_247025,RMVar_hsa_circ_247023,RMVar_hsa_circ_50989,RMVar_hsa_circ_118130,RMVar_hsa_circ_247028,RMVar_hsa_circ_90521,RMVar_hsa_circ_247029,RMVar_hsa_circ_35518 74417 RMVar_ID_74417 Human_SNP_ID_332557979 m1A Human chr7 + 100096105 100096105 100096105 CCCACCCTCTAAGGTCAGTTCTCCACTCACGGAGTCTCTCAGCACAGCTGCCGTAAGCCCCACTC CCCACCCTCTAAGGTCAGTTCTCCACTCACGGGGTCTCTCAGCACAGCTGCCGTAAGCCCCACTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr7:100095839..100096113;chr7:100095751..100096175 26863196,32194978 MeRIP-seq:(Medium) rs767723414 Functional Loss SNV dbSNP153 33..33 33 - - - 74418 RMVar_ID_74418 Human_SNP_ID_332558522 m1A Human chr7 + 100097370 100097370 100097370 AGACTTGGCCACACCAGGATCCCCCATCAGACAGATGTTGATGTTGCCTGGAGGAAGGGAAGGCA AGACTTGGCCACACCAGGATCCCCCATCAGACGGATGTTGATGTTGCCTGGAGGAAGGGAAGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100097272..100097405 26863196 MeRIP-seq:(Medium) rs773395941 Functional Loss SNV dbSNP153 33..33 33 - - - 74419 RMVar_ID_74419 Human_SNP_ID_332558692 m1A Human chr7 - 100097745 100097745 100097745 CAGAAAATAAAACAACCTTAACTTCTCTACAGAGGAGGATTTCTACGAAAAGCTGGCAGCTTCAA CAGAAAATAAAACAACCTTAACTTCTCTACAGTGGAGGATTTCTACGAAAAGCTGGCAGCTTCAA T A MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100097723..100097824 26863196 MeRIP-seq:(Medium) rs1296508100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85512,Human_RBP_ID_954686,Human_RBP_ID_5401615,Human_RBP_ID_7778073,Human_RBP_ID_9403675,Human_RBP_ID_22516404,Human_RBP_ID_26356779,Human_RBP_ID_27829588 Human_Splice_Rec_896870,Human_Splice_Rec_896898,Human_Splice_Rec_896924,Human_Splice_Rec_896950,Human_Splice_Rec_896992 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,RMVar_hsa_circ_107157,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_106455,RMVar_hsa_circ_96816,RMVar_hsa_circ_247018,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_247015,RMVar_hsa_circ_49459,RMVar_hsa_circ_61503,RMVar_hsa_circ_341554,RMVar_hsa_circ_373853,RMVar_hsa_circ_107879,RMVar_hsa_circ_247024,RMVar_hsa_circ_247026,RMVar_hsa_circ_247025,RMVar_hsa_circ_118130,RMVar_hsa_circ_247028,RMVar_hsa_circ_90521,RMVar_hsa_circ_113385,RMVar_hsa_circ_247029,RMVar_hsa_circ_35518,RMVar_hsa_circ_119373,RMVar_hsa_circ_247031,RMVar_hsa_circ_107288,RMVar_hsa_circ_247032,RMVar_hsa_circ_247033 74420 RMVar_ID_74420 Human_SNP_ID_332558746 m1A Human chr7 - 100097851 100097851 100097851 TGAGTCTGGGGCTGGAGAGCTCACCAGGGAGGAGCTGAGGCAAATTGCAGGTGAGGGGCAGGGGA TGAGTCTGGGGCTGGAGAGCTCACCAGGGAGGTGCTGAGGCAAATTGCAGGTGAGGGGCAGGGGA T A MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100097826..100097850 26863196 MeRIP-seq:(Medium) rs1198657506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253717,Human_RBP_ID_267837,Human_RBP_ID_793868,Human_RBP_ID_844045,Human_RBP_ID_954687,Human_RBP_ID_1053725,Human_RBP_ID_1690772,Human_RBP_ID_3971076,Human_RBP_ID_5401616,Human_RBP_ID_7778074,Human_RBP_ID_8914141,Human_RBP_ID_9311389,Human_RBP_ID_9403677,Human_RBP_ID_18107816,Human_RBP_ID_18171936,Human_RBP_ID_19021142,Human_RBP_ID_19135208,Human_RBP_ID_22463219,Human_RBP_ID_22835833,Human_RBP_ID_23079816,Human_RBP_ID_24234934,Human_RBP_ID_24549293,Human_RBP_ID_26129410,Human_RBP_ID_26356030,Human_RBP_ID_27830569 Human_Splice_Rec_896868,Human_Splice_Rec_896869,Human_Splice_Rec_896896,Human_Splice_Rec_896897,Human_Splice_Rec_896922,Human_Splice_Rec_896923,Human_Splice_Rec_896948,Human_Splice_Rec_896949,Human_Splice_Rec_896976,Human_Splice_Rec_896977,Human_Splice_Rec_896990,Human_Splice_Rec_896991 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,RMVar_hsa_circ_107157,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_106455,RMVar_hsa_circ_96816,RMVar_hsa_circ_247018,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_247015,RMVar_hsa_circ_49459,RMVar_hsa_circ_61503,RMVar_hsa_circ_341554,RMVar_hsa_circ_373853,RMVar_hsa_circ_107879,RMVar_hsa_circ_247024,RMVar_hsa_circ_247026,RMVar_hsa_circ_247025,RMVar_hsa_circ_118130,RMVar_hsa_circ_247028,RMVar_hsa_circ_90521,RMVar_hsa_circ_113385,RMVar_hsa_circ_247029,RMVar_hsa_circ_35518,RMVar_hsa_circ_119373,RMVar_hsa_circ_247031,RMVar_hsa_circ_107288,RMVar_hsa_circ_127795,RMVar_hsa_circ_247032,RMVar_hsa_circ_247033,RMVar_hsa_circ_247035,RMVar_hsa_circ_76895,RMVar_hsa_circ_247034 74421 RMVar_ID_74421 Human_SNP_ID_332558760 m1A Human chr7 + 100097879 100097879 100097879 CAGCTCCTCCCTGGTGAGCTCTCCAGCCCCAGACTCATCATCCTCACTCTTGTTCATCTTCACAA CAGCTCCTCCCTGGTGAGCTCTCCAGCCCCAGGCTCATCATCCTCACTCTTGTTCATCTTCACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100097614..100097933 26863196 MeRIP-seq:(Medium) rs1375413651 Functional Loss SNV dbSNP153 33..33 33 - - - 74422 RMVar_ID_74422 Human_SNP_ID_332558776 m1A Human chr7 + 100097939 100097937 100097939 CACAATCCGATGGGCTTCCAGGTAGGTTTCTGAGAGTAAACCCTTGGGCAGGAAAATGCCAGGAT CACAATCCGATGGGCTTCCAGGTAGGTTTCT__GAGTAAACCCTTGGGCAGGAAAATGCCAGGAT TGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100097826..100097950 32194978 MeRIP-seq:(Medium) rs1191182207 Functional Loss DEL dbSNP153 32..33 33 - - - 74423 RMVar_ID_74423 Human_SNP_ID_332558859 m1A Human chr7 + 100098103 100098103 100098103 TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAAAGGGGATGATCCATTCCTCATGTCAAACTCTTC TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAACGGGGATGATCCATTCCTCATGTCAAACTCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100098102..100098302 26863196 MeRIP-seq:(Medium) rs369912024 Functional Loss SNV dbSNP153 33..33 33 - - - 74424 RMVar_ID_74424 Human_SNP_ID_332558860 m1A Human chr7 + 100098103 100098103 100098103 TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAAAGGGGATGATCCATTCCTCATGTCAAACTCTTC TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAAGGGGGATGATCCATTCCTCATGTCAAACTCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100098102..100098302 26863196 MeRIP-seq:(Medium) rs369912024 Functional Loss SNV dbSNP153 33..33 33 - - - 74425 RMVar_ID_74425 Human_SNP_ID_332558920 m1A Human chr7 - 100098225 100098225 100098225 AGTATCACGGTGCTGGTAGAAGGAGAGAACACAAGGATTGCCCAGCCTGGAGACCACGTCAGCGT AGTATCACGGTGCTGGTAGAAGGAGAGAACACGAGGATTGCCCAGCCTGGAGACCACGTCAGCGT T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100098121..100098237 26863196 MeRIP-seq:(Medium) rs750861183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85516,Human_RBP_ID_253718,Human_RBP_ID_1690779,Human_RBP_ID_2050403,Human_RBP_ID_3860088,Human_RBP_ID_4955164,Human_RBP_ID_5219450,Human_RBP_ID_5623204,Human_RBP_ID_7778080,Human_RBP_ID_8272053,Human_RBP_ID_8675776,Human_RBP_ID_8914150,Human_RBP_ID_16270508,Human_RBP_ID_17713756,Human_RBP_ID_18195999,Human_RBP_ID_18888689,Human_RBP_ID_19021144,Human_RBP_ID_22464623,Human_RBP_ID_22835836,Human_RBP_ID_23079822,Human_RBP_ID_24234936,Human_RBP_ID_27118967 Human_Splice_Rec_896866,Human_Splice_Rec_896867,Human_Splice_Rec_896894,Human_Splice_Rec_896895,Human_Splice_Rec_896920,Human_Splice_Rec_896921,Human_Splice_Rec_896946,Human_Splice_Rec_896947,Human_Splice_Rec_896974,Human_Splice_Rec_896975,Human_Splice_Rec_896988,Human_Splice_Rec_896989,Human_Splice_Rec_897022,Human_Splice_Rec_897034 Human_miRNA_ID_2490105,Human_miRNA_ID_2490106,Human_miRNA_ID_2752188,Human_miRNA_ID_2752189 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_106455,RMVar_hsa_circ_96816,RMVar_hsa_circ_247018,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_49459,RMVar_hsa_circ_61503,RMVar_hsa_circ_341554,RMVar_hsa_circ_373853,RMVar_hsa_circ_247026,RMVar_hsa_circ_247025,RMVar_hsa_circ_118130,RMVar_hsa_circ_247028,RMVar_hsa_circ_90521,RMVar_hsa_circ_113385,RMVar_hsa_circ_247029,RMVar_hsa_circ_35518,RMVar_hsa_circ_119373,RMVar_hsa_circ_247031,RMVar_hsa_circ_107288,RMVar_hsa_circ_127795,RMVar_hsa_circ_247032,RMVar_hsa_circ_247033,RMVar_hsa_circ_247035,RMVar_hsa_circ_76895,RMVar_hsa_circ_247034 74426 RMVar_ID_74426 Human_SNP_ID_332559124 m1A Human chr7 + 100098714 100098714 100098714 ACATGATCAGAGGCATGAAAGTGGGAGACTGGATCTAGGATGTGAGAACAGAAACACCAAAGGAA ACATGATCAGAGGCATGAAAGTGGGAGACTGGTTCTAGGATGTGAGAACAGAAACACCAAAGGAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100098572..100098743 26863196 MeRIP-seq:(Medium) rs775851630 Functional Loss SNV dbSNP153 33..33 33 - - - 74427 RMVar_ID_74427 Human_SNP_ID_332559379 m1A Human chr7 + 100099229 100099229 100099229 CAGCTCACTAAGGGGAGAAAACAGTCACAAACAAGATCCTGGAGAACCAATCCCTACATCTTTCC CAGCTCACTAAGGGGAGAAAACAGTCACAAACGAGATCCTGGAGAACCAATCCCTACATCTTTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100099226..100099275 32194978 MeRIP-seq:(Medium) rs370793797 Functional Loss SNV dbSNP153 33..33 33 - - - 74428 RMVar_ID_74428 Human_SNP_ID_332559451 m1A Human chr7 - 100099355 100099355 100099355 TCCTGGACGTTTACATTGAGCATCGGCTAATGATGGAGCAGCGGAGTCGGGACCCTGGGATGGTC TCCTGGACGTTTACATTGAGCATCGGCTAATGGTGGAGCAGCGGAGTCGGGACCCTGGGATGGTC T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs149343096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85521,Human_RBP_ID_253722,Human_RBP_ID_1053736,Human_RBP_ID_1333824,Human_RBP_ID_1400063,Human_RBP_ID_1690795,Human_RBP_ID_2050417,Human_RBP_ID_3860097,Human_RBP_ID_4966485,Human_RBP_ID_5221669,Human_RBP_ID_5623206,Human_RBP_ID_7778091,Human_RBP_ID_8272054,Human_RBP_ID_8675794,Human_RBP_ID_8914170,Human_RBP_ID_9311392,Human_RBP_ID_9403683,Human_RBP_ID_16270535,Human_RBP_ID_17314394,Human_RBP_ID_18888704,Human_RBP_ID_22464147,Human_RBP_ID_22835852,Human_RBP_ID_23080352,Human_RBP_ID_24234954,Human_RBP_ID_26130592,Human_RBP_ID_26356785,Human_RBP_ID_27361376 Human_Splice_Rec_896862,Human_Splice_Rec_896888,Human_Splice_Rec_896889,Human_Splice_Rec_896916,Human_Splice_Rec_896942,Human_Splice_Rec_896968,Human_Splice_Rec_896969,Human_Splice_Rec_896984,Human_Splice_Rec_897028,Human_Splice_Rec_897029 RMVar_hsa_circ_5850,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_106455,RMVar_hsa_circ_247018,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_61503,RMVar_hsa_circ_341554,RMVar_hsa_circ_373853,RMVar_hsa_circ_247026,RMVar_hsa_circ_247025,RMVar_hsa_circ_90521,RMVar_hsa_circ_113385,RMVar_hsa_circ_247029,RMVar_hsa_circ_247031,RMVar_hsa_circ_127795,RMVar_hsa_circ_247034,RMVar_hsa_circ_120691,RMVar_hsa_circ_378197,RMVar_hsa_circ_247038,RMVar_hsa_circ_247039 74429 RMVar_ID_74429 Human_SNP_ID_332559475 m1A Human chr7 + 100099395 100099391 100099395 CGATGCTCAATGTAAACGTCCAGGACATCTTTATTTACCACCTAAAGGAGAAGAACAAAAAAAAA CGATGCTCAATGTAAACGTCCAGGACATC____TTTACCACCTAAAGGAGAAGAACAAAAAAAAA CTTTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100099276..100099409 26863196 MeRIP-seq:(Medium) rs775276253 Functional Loss DEL dbSNP153 30..33 33 - - - 74430 RMVar_ID_74430 Human_SNP_ID_332559480 m1A Human chr7 + 100099395 100099395 100099395 CGATGCTCAATGTAAACGTCCAGGACATCTTTATTTACCACCTAAAGGAGAAGAACAAAAAAAAA CGATGCTCAATGTAAACGTCCAGGACATCTTTTTTTACCACCTAAAGGAGAAGAACAAAAAAAAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100099276..100099409 26863196 MeRIP-seq:(Medium) rs764691803 Functional Loss SNV dbSNP153 33..33 33 - - - 74431 RMVar_ID_74431 Human_SNP_ID_332559884 m1A Human chr7 - 100100072 100100072 100100072 TCATGTTACAGAAAAGGTTAAGAAGTTCTTACAAGAGTTCTACCAGGATGATGAACTCGGGAAGA TCATGTTACAGAAAAGGTTAAGAAGTTCTTACGAGAGTTCTACCAGGATGATGAACTCGGGAAGA T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100099976..100100133;chr7:100099993..100100118;chr7:100100001..100100100 26863196 MeRIP-seq:(Medium) rs771850757 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_85524,Human_RBP_ID_957159,Human_RBP_ID_1053739,Human_RBP_ID_1690813,Human_RBP_ID_2050425,Human_RBP_ID_3860103,Human_RBP_ID_4955198,Human_RBP_ID_8675805,Human_RBP_ID_9311090,Human_RBP_ID_9403687,Human_RBP_ID_16270558,Human_RBP_ID_17713760,Human_RBP_ID_18107827,Human_RBP_ID_18888714,Human_RBP_ID_19021147,Human_RBP_ID_19136942,Human_RBP_ID_22464631,Human_RBP_ID_23079842,Human_RBP_ID_24234962,Human_RBP_ID_26129445,Human_RBP_ID_26356036,Human_RBP_ID_27118984 Human_Splice_Rec_896858,Human_Splice_Rec_896859,Human_Splice_Rec_896884,Human_Splice_Rec_896885,Human_Splice_Rec_896912,Human_Splice_Rec_896913,Human_Splice_Rec_896938,Human_Splice_Rec_896939,Human_Splice_Rec_896964,Human_Splice_Rec_896965,Human_Splice_Rec_896980,Human_Splice_Rec_896981,Human_Splice_Rec_897016,Human_Splice_Rec_897017,Human_Splice_Rec_897024,Human_Splice_Rec_897025,Human_Splice_Rec_897036,Human_Splice_Rec_897037,Human_Splice_Rec_897040,Human_Splice_Rec_897041,Human_Splice_Rec_897043 RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_61503,RMVar_hsa_circ_341554,RMVar_hsa_circ_247026,RMVar_hsa_circ_113385,RMVar_hsa_circ_247031,RMVar_hsa_circ_91352,RMVar_hsa_circ_127795,RMVar_hsa_circ_247034,RMVar_hsa_circ_247040 74432 RMVar_ID_74432 Human_SNP_ID_332559899 m1A Human chr7 - 100100095 100100095 100100095 TTTGTGTCTTACGGTTTTACATTTCATGTTACAGAAAAGGTTAAGAAGTTCTTACAAGAGTTCTA TTTGTGTCTTACGGTTTTACATTTCATGTTACGGAAAAGGTTAAGAAGTTCTTACAAGAGTTCTA T C MCM7 Ensembl:ENSG00000166508 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100100051..100100100 32194978 MeRIP-seq:(Medium) rs762955038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26129447 Human_Splice_Rec_896859,Human_Splice_Rec_896885,Human_Splice_Rec_896913,Human_Splice_Rec_896939,Human_Splice_Rec_896965,Human_Splice_Rec_896981,Human_Splice_Rec_897017,Human_Splice_Rec_897025,Human_Splice_Rec_897037,Human_Splice_Rec_897041,Human_Splice_Rec_897043 RMVar_hsa_circ_112139,RMVar_hsa_circ_247021,RMVar_hsa_circ_113385,RMVar_hsa_circ_247031,RMVar_hsa_circ_91352,RMVar_hsa_circ_247040 74433 RMVar_ID_74433 Human_SNP_ID_332560533 m1A Human chr7 - 100101322 100101322 100101322 GCTTCCCCAGGAGCAAGACCTCTGAGCCCGCCAAGCGCGGCCGCACGGCCCTCGGCAGCGATGGC GCTTCCCCAGGAGCAAGACCTCTGAGCCCGCCGAGCGCGGCCGCACGGCCCTCGGCAGCGATGGC T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100101276..100101325 26863196 MeRIP-seq:(Medium) rs1322913619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85525,Human_RBP_ID_175237,Human_RBP_ID_253725,Human_RBP_ID_1690818,Human_RBP_ID_4956516,Human_RBP_ID_5327932,Human_RBP_ID_8915034,Human_RBP_ID_9311396,Human_RBP_ID_9337261,Human_RBP_ID_9403689,Human_RBP_ID_16270566,Human_RBP_ID_22464632,Human_RBP_ID_22835862,Human_RBP_ID_23080678,Human_RBP_ID_26356037,Human_RBP_ID_27118986,Human_RBP_ID_27361384,Human_RBP_ID_27534705 Human_Splice_Rec_896857,Human_Splice_Rec_896883,Human_Splice_Rec_896937,Human_Splice_Rec_896963,Human_Splice_Rec_897015 RMVar_hsa_circ_112139,RMVar_hsa_circ_247021,RMVar_hsa_circ_113385,RMVar_hsa_circ_247031,RMVar_hsa_circ_91352,RMVar_hsa_circ_247040 74434 RMVar_ID_74434 Human_SNP_ID_332560544 m1A Human chr7 - 100101337 100101337 100101337 GCGCGGAGATTCTCAGCTTCCCCAGGAGCAAGACCTCTGAGCCCGCCAAGCGCGGCCGCACGGCC GCGCGGAGATTCTCAGCTTCCCCAGGAGCAAGCCCTCTGAGCCCGCCAAGCGCGGCCGCACGGCC T G MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:100101168..100101400;chr7:100101011..100101400;chr7:100101062..100101400;chr7:100101188..100101400 26863196 MeRIP-seq:(Medium) rs780947160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85525,Human_RBP_ID_175237,Human_RBP_ID_253725,Human_RBP_ID_691407,Human_RBP_ID_1223009,Human_RBP_ID_1333825,Human_RBP_ID_1690818,Human_RBP_ID_4956516,Human_RBP_ID_5327932,Human_RBP_ID_8915034,Human_RBP_ID_9311396,Human_RBP_ID_9337261,Human_RBP_ID_9403689,Human_RBP_ID_18888718,Human_RBP_ID_22464632,Human_RBP_ID_22835862,Human_RBP_ID_23080678,Human_RBP_ID_26356037,Human_RBP_ID_27118986,Human_RBP_ID_27361384,Human_RBP_ID_27534705 Human_Splice_Rec_896857,Human_Splice_Rec_896883,Human_Splice_Rec_896937,Human_Splice_Rec_896963,Human_Splice_Rec_897015 Human_miRNA_ID_2269145,Human_miRNA_ID_2611126 RMVar_hsa_circ_112139,RMVar_hsa_circ_247021,RMVar_hsa_circ_113385,RMVar_hsa_circ_247031,RMVar_hsa_circ_91352,RMVar_hsa_circ_247040 74435 RMVar_ID_74435 Human_SNP_ID_332563176 m1A Human chr7 - 100107199 100107199 100107199 GCCCCCGGATTCCCACACATGCAGACATGTACACACGTGCACGTACACACATGCATGCTCGCTAA GCCCCCGGATTCCCACACATGCAGACATGTACGCACGTGCACGTACACACATGCATGCTCGCTAA T C TAF6 Ensembl:ENSG00000106290 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:100107101..100107575 26863196 MeRIP-seq:(Medium) rs1215441580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691413,Human_RBP_ID_17314704,Human_RBP_ID_17427036,Human_RBP_ID_17543145,Human_RBP_ID_18888722 Human_miRNA_ID_2729447 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 74436 RMVar_ID_74436 Human_SNP_ID_332563280 m1A Human chr7 - 100107399 100107399 100107399 GGCAAAGGAGGCCCCACCTCCCATCCTTCTCCAGTTCCTCCCCCGGCATCGTCCCCGTCCCCACT GGCAAAGGAGGCCCCACCTCCCATCCTTCTCCTGTTCCTCCCCCGGCATCGTCCCCGTCCCCACT T A TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100107216..100107450 26863196 MeRIP-seq:(Medium) rs752995974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691419,Human_RBP_ID_17316154,Human_RBP_ID_18960240 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 74437 RMVar_ID_74437 Human_SNP_ID_332563309 m1A Human chr7 - 100107461 100107461 100107461 CTCCCTCTGGTCCTGGGAGTGTCCAGAAGTACATCGTGGTCTCACTTCCCCCAACAGGGGAGGGC CTCCCTCTGGTCCTGGGAGTGTCCAGAAGTACGTCGTGGTCTCACTTCCCCCAACAGGGGAGGGC T C TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100107410..100107640 26863196 MeRIP-seq:(Medium) rs1339382108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691420,Human_RBP_ID_1690822,Human_RBP_ID_4955231,Human_RBP_ID_8675817 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 74438 RMVar_ID_74438 Human_SNP_ID_332563363 m1A Human chr7 - 100107591 100107591 100107591 GTCCTGTCCCTCAGCACCTCGGCCCCCGGCTCAGGTTCCACCACCACTTCGCCCGTCACCACCAC GTCCTGTCCCTCAGCACCTCGGCCCCCGGCTCGGGTTCCACCACCACTTCGCCCGTCACCACCAC T C TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100107151..100108125 26863196 MeRIP-seq:(Medium) rs768942294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253194,Human_RBP_ID_4955237,Human_RBP_ID_17427041 Human_Splice_Rec_897372,Human_Splice_Rec_897400,Human_Splice_Rec_897426,Human_Splice_Rec_897454,Human_Splice_Rec_897482,Human_Splice_Rec_897510 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 74439 RMVar_ID_74439 Human_SNP_ID_332563364 m1A Human chr7 - 100107591 100107591 100107591 GTCCTGTCCCTCAGCACCTCGGCCCCCGGCTCAGGTTCCACCACCACTTCGCCCGTCACCACCAC GTCCTGTCCCTCAGCACCTCGGCCCCCGGCTCCGGTTCCACCACCACTTCGCCCGTCACCACCAC T G TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100107151..100108125 26863196 MeRIP-seq:(Medium) rs768942294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253194,Human_RBP_ID_4955237,Human_RBP_ID_17427041 Human_Splice_Rec_897372,Human_Splice_Rec_897400,Human_Splice_Rec_897426,Human_Splice_Rec_897454,Human_Splice_Rec_897482,Human_Splice_Rec_897510 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 74440 RMVar_ID_74440 Human_SNP_ID_332563556 m1A Human chr7 + 100108070 100108070 100108070 AGTGCGATGGAGCCAGGAACCTTCAGCAAGCCAGGGGTGCGAGGGCCAGGCTGTGGGGCCTGCGA AGTGCGATGGAGCCAGGAACCTTCAGCAAGCCCGGGGTGCGAGGGCCAGGCTGTGGGGCCTGCGA A C AP4M1 Ensembl:ENSG00000221838 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100108019..100108462 32194978 MeRIP-seq:(Medium) rs754052943 Functional Loss SNV dbSNP153 33..33 33 - - - 74441 RMVar_ID_74441 Human_SNP_ID_332564243 m1A Human chr7 - 100110019 100110019 100110019 CCCGGCTGCAGCAGGAAGGGGAGCGGATCCGCAGTGTGCTGGACGGCCCTGTGCTGAGCAACATT CCCGGCTGCAGCAGGAAGGGGAGCGGATCCGCGGTGTGCTGGACGGCCCTGTGCTGAGCAACATT T C TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100109968..100110068 32194978 MeRIP-seq:(Medium) rs768178481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691424,Human_RBP_ID_957069,Human_RBP_ID_4955248,Human_RBP_ID_5404301,Human_RBP_ID_9215825,Human_RBP_ID_18196310,Human_RBP_ID_18472350,Human_RBP_ID_19019899,Human_RBP_ID_26131115 Human_Splice_Rec_897366,Human_Splice_Rec_897367,Human_Splice_Rec_897394,Human_Splice_Rec_897395,Human_Splice_Rec_897420,Human_Splice_Rec_897421,Human_Splice_Rec_897448,Human_Splice_Rec_897449,Human_Splice_Rec_897476,Human_Splice_Rec_897477,Human_Splice_Rec_897504,Human_Splice_Rec_897505 Human_miRNA_ID_2572949 RMVar_hsa_circ_102089,RMVar_hsa_circ_22802,RMVar_hsa_circ_42178,RMVar_hsa_circ_107503,RMVar_hsa_circ_247055,RMVar_hsa_circ_247056,RMVar_hsa_circ_86986,RMVar_hsa_circ_370499,RMVar_hsa_circ_247057,RMVar_hsa_circ_247058 74442 RMVar_ID_74442 Human_SNP_ID_332565339 m1A Human chr7 + 100113382 100113382 100113382 TGGGGGCGGGTTCTCGGGGATAGCTGGCTGGCAGCCCTCGATGCTCAGCCAATGAGCTGCAAGGA TGGGGGCGGGTTCTCGGGGATAGCTGGCTGGCTGCCCTCGATGCTCAGCCAATGAGCTGCAAGGA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100113359..100113460 32194978 MeRIP-seq:(Medium) rs1187138055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247059 74443 RMVar_ID_74443 Human_SNP_ID_332565716 m1A Human chr7 - 100114193 100114191 100114194 GAAGAGGGACTCCAGAATGGCTGAGGAGAAGAAGCTGAAGCTTAGCAACACTGTGCTGCCCTCGG GAAGAGGGACTCCAGAATGGCTGAGGAGAAG___CTGAAGCTTAGCAACACTGTGCTGCCCTCGG GCTT G TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100114065..100114270 26863196 MeRIP-seq:(Medium) rs775448824 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2050436,Human_RBP_ID_4956518,Human_RBP_ID_9403692,Human_RBP_ID_16270614,Human_RBP_ID_18196311,Human_RBP_ID_19021155,Human_RBP_ID_22516409,Human_RBP_ID_26140229,Human_RBP_ID_27569525 Human_Splice_Rec_897346,Human_Splice_Rec_897374,Human_Splice_Rec_897428,Human_Splice_Rec_897456,Human_Splice_Rec_897484,Human_Splice_Rec_897514,Human_Splice_Rec_897528,Human_Splice_Rec_897542,Human_Splice_Rec_897554,Human_Splice_Rec_897564,Human_Splice_Rec_897572,Human_Splice_Rec_897580,Human_Splice_Rec_897588,Human_Splice_Rec_897596,Human_Splice_Rec_897602,Human_Splice_Rec_897608,Human_Splice_Rec_897612 RMVar_hsa_circ_70570 74444 RMVar_ID_74444 Human_SNP_ID_332567168 m1A Human chr7 - 100119304 100119304 100119304 AGCGCCGGGTGAGCAGCGTCTCGGCTGCCGCTAGAGTTTTCCTGCTCCCCGCGCTCGGGTGGCGG AGCGCCGGGTGAGCAGCGTCTCGGCTGCCGCTGGAGTTTTCCTGCTCCCCGCGCTCGGGTGGCGG T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100119133..100119375 26863196 MeRIP-seq:(Medium) rs901087618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254006,Human_RBP_ID_4955314,Human_RBP_ID_9311397,Human_RBP_ID_9403693,Human_RBP_ID_18426063 Human_Splice_Rec_897593 74445 RMVar_ID_74445 Human_SNP_ID_332567178 m1A Human chr7 + 100119318 100119318 100119318 CGGGGAGCAGGAAAACTCTAGCGGCAGCCGAGACGCTGCTCACCCGGCGCTCGGCGCCATCTTGG CGGGGAGCAGGAAAACTCTAGCGGCAGCCGAGGCGCTGCTCACCCGGCGCTCGGCGCCATCTTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100119121..100119350 26863196 MeRIP-seq:(Medium) rs1324328108 Functional Loss SNV dbSNP153 33..33 33 - - - 74446 RMVar_ID_74446 Human_SNP_ID_332567332 m1A Human chr7 - 100119722 100119722 100119722 CAGGTCCCATGACAAAGCGCCGTCTACAAACAATCACCGCTTGCCTTCAACTTCGGGAAGGTAGT CAGGTCCCATGACAAAGCGCCGTCTACAAACAGTCACCGCTTGCCTTCAACTTCGGGAAGGTAGT T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100119672..100119891 26863196 MeRIP-seq:(Medium) rs757835840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_897483 74447 RMVar_ID_74447 Human_SNP_ID_332567338 m1A Human chr7 + 100119732 100119732 100119732 CGAAGTTGAAGGCAAGCGGTGATTGTTTGTAGACGGCGCTTTGTCATGGGACCTGTGCGGTTGGG CGAAGTTGAAGGCAAGCGGTGATTGTTTGTAGGCGGCGCTTTGTCATGGGACCTGTGCGGTTGGG A G CNPY4 Ensembl:ENSG00000166997 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100119686..100119831 26863196 MeRIP-seq:(Medium) rs1387341674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16270710 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795 74448 RMVar_ID_74448 Human_SNP_ID_332567377 m1A Human chr7 - 100119812 100119812 100119812 AGCGTTCTGTGTCATCGTCCTCCTCCTTCAACATCCCAGCCCAAGCCTCGTGCACGGCCAAAAAA AGCGTTCTGTGTCATCGTCCTCCTCCTTCAACGTCCCAGCCCAAGCCTCGTGCACGGCCAAAAAA T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100119689..100119886 26863196 MeRIP-seq:(Medium) rs1231711239 Functional Loss SNV dbSNP153 33..33 33 - - - 74449 RMVar_ID_74449 Human_SNP_ID_332567379 m1A Human chr7 + 100119818 100119815 100119818 GGCCGTGCACGAGGCTTGGGCTGGGATGTTGAAGGAGGAGGACGATGACACAGAACGCTTGCCCA GGCCGTGCACGAGGCTTGGGCTGGGATGTT___GGAGGAGGACGATGACACAGAACGCTTGCCCA TGAA T CNPY4 Ensembl:ENSG00000166997 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100119705..100119878 26863196 MeRIP-seq:(Medium) rs758379452 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_793884,Human_RBP_ID_24234987 Human_Splice_Rec_897615 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795 74450 RMVar_ID_74450 Human_SNP_ID_332567381 m1A Human chr7 + 100119818 100119818 100119818 GGCCGTGCACGAGGCTTGGGCTGGGATGTTGAAGGAGGAGGACGATGACACAGAACGCTTGCCCA GGCCGTGCACGAGGCTTGGGCTGGGATGTTGAGGGAGGAGGACGATGACACAGAACGCTTGCCCA A G CNPY4 Ensembl:ENSG00000166997 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100119705..100119878 26863196 MeRIP-seq:(Medium) rs757891301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793884,Human_RBP_ID_24234987 Human_Splice_Rec_897615 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795 74451 RMVar_ID_74451 Human_SNP_ID_332569141 m1A Human chr7 + 100124834 100124834 100124834 GAGGAGGAGGAAGAGGAGGAAGAGGAAGGGGGAGACAAGATGACCAAGACAGGAAGCCACCCCAA GAGGAGGAGGAAGAGGAGGAAGAGGAAGGGGGCGACAAGATGACCAAGACAGGAAGCCACCCCAA A C CNPY4 Ensembl:ENSG00000166997 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100124783..100124909 26863196 MeRIP-seq:(Medium) rs1397198665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22775009 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795,RMVar_hsa_circ_247064,RMVar_hsa_circ_127948 74452 RMVar_ID_74452 Human_SNP_ID_332569241 m1A Human chr7 - 100125134 100125134 100125134 AGAGGAAAGCTTTCAGTACTGTCAGCACATACACCTGCCAATTAAGGGGCTGGATAGAGTTCATC AGAGGAAAGCTTTCAGTACTGTCAGCACATACGCCTGCCAATTAAGGGGCTGGATAGAGTTCATC T C AC073842.2 Ensembl:ENSG00000242798 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100125091..100125376 26863196 MeRIP-seq:(Medium) rs992963330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251388 74453 RMVar_ID_74453 Human_SNP_ID_332570231 m1A Human chr7 - 100128002 100128002 100128002 CTGGGCTGCGGGGTCTTCACTCAGTGCCTGCCACGAATCCTCGTCCCCATCTCGCTCAAACACAT CTGGGCTGCGGGGTCTTCACTCAGTGCCTGCCGCGAATCCTCGTCCCCATCTCGCTCAAACACAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:100127591..100128056;chr7:100127695..100128003 26863196 MeRIP-seq:(Medium) rs1391455036 Functional Loss SNV dbSNP153 33..33 33 - - - 74454 RMVar_ID_74454 Human_SNP_ID_332582455 m1A Human chr7 - 100170203 100170203 100170203 CGATAACGGGGGAGGGGTGCCCTAGCATCAGAAGGGTTCATGGCCCTTTCCCCTCCTCCCCCCTC CGATAACGGGGGAGGGGTGCCCTAGCATCAGAGGGGTTCATGGCCCTTTCCCCTCCTCCCCCCTC T C GPC2 Ensembl:ENSG00000213420 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100170152..100170252 32194978 MeRIP-seq:(Medium) rs781590863 Functional Loss SNV dbSNP153 33..33 33 - - - 74455 RMVar_ID_74455 Human_SNP_ID_332584930 m1A Human chr7 - 100177315 100177315 100177315 GCTATCGTGCTCGGTATTCAGTTTTCCGGAGCAGCGCTCTTTCTCTGGCCCGCGGAGCGGTCCCG GCTATCGTGCTCGGTATTCAGTTTTCCGGAGCGGCGCTCTTTCTCTGGCCCGCGGAGCGGTCCCG T C GPC2 Ensembl:ENSG00000213420 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100177268..100177339 26863196 MeRIP-seq:(Medium) rs1168612749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94004,RMVar_hsa_circ_247074 74456 RMVar_ID_74456 Human_SNP_ID_332593060 m1A Human chr7 + 100209906 100209906 100209906 GGAAGGCAGAGAGTGAAGATAGCTGTGGGGGAAGGTTGGGGCATTGGTGTTGGCCACAGGATTAC GGAAGGCAGAGAGTGAAGATAGCTGTGGGGGAGGGTTGGGGCATTGGTGTTGGCCACAGGATTAC A G STAG3 Ensembl:ENSG00000066923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100209857..100209955 26863196 MeRIP-seq:(Medium) rs1305218167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98036,RMVar_hsa_circ_247075 74457 RMVar_ID_74457 Human_SNP_ID_332596462 m1A Human chr7 - 100220915 100220915 100220915 TGGGAGGCCTGGCTTGGTGCCTGCGCGGGGGAAGGAGGGTCAAGTGAGTCTGCACAGCTTGGGCC TGGGAGGCCTGGCTTGGTGCCTGCGCGGGGGATGGAGGGTCAAGTGAGTCTGCACAGCTTGGGCC T A CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100220877..100220977 26863196 MeRIP-seq:(Medium) rs749063283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267839,Human_RBP_ID_8730539 RMVar_hsa_circ_88038,RMVar_hsa_circ_247081 74458 RMVar_ID_74458 Human_SNP_ID_332596463 m1A Human chr7 - 100220915 100220915 100220915 TGGGAGGCCTGGCTTGGTGCCTGCGCGGGGGAAGGAGGGTCAAGTGAGTCTGCACAGCTTGGGCC TGGGAGGCCTGGCTTGGTGCCTGCGCGGGGGACGGAGGGTCAAGTGAGTCTGCACAGCTTGGGCC T G CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100220877..100220977 26863196 MeRIP-seq:(Medium) rs749063283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267839,Human_RBP_ID_8730539 RMVar_hsa_circ_88038,RMVar_hsa_circ_247081 74459 RMVar_ID_74459 Human_SNP_ID_332597119 m1A Human chr7 - 100222909 100222909 100222909 CCAGGCAGCCAGCACAGCATGTGCAAAGGCCCAGGGGCCTGAGAGTGAGATGGAGAATCAGGACG CCAGGCAGCCAGCACAGCATGTGCAAAGGCCCCGGGGCCTGAGAGTGAGATGGAGAATCAGGACG T G CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:100222859..100223002 26863196 MeRIP-seq:(Medium) rs961785112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299180 74460 RMVar_ID_74460 Human_SNP_ID_332599323 m1A Human chr7 + 100231369 100231369 100231369 TTTCCCTGCCTACCTCTGTCTTCCCCTTTTTTACGTGCTGGACCTGGCCCTTGCTTCTGCTCCTG TTTCCCTGCCTACCTCTGTCTTCCCCTTTTTTGCGTGCTGGACCTGGCCCTTGCTTCTGCTCCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100231333..100231438 26863196 MeRIP-seq:(Medium) rs1466647277 Functional Loss SNV dbSNP153 33..33 33 - - - 74461 RMVar_ID_74461 Human_SNP_ID_332602917 m1A Human chr7 - 100246571 100246571 100246571 AGCCATGTGGGTCCAGGCAACAGGTCATGGGCAGGGAGGCACAAGGGAAGACGTCATCGGGCTGG AGCCATGTGGGTCCAGGCAACAGGTCATGGGCGGGGAGGCACAAGGGAAGACGTCATCGGGCTGG T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100246377..100246636 26863196 MeRIP-seq:(Medium) rs1473455654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93743,RMVar_hsa_circ_247084 74462 RMVar_ID_74462 Human_SNP_ID_332602920 m1A Human chr7 - 100246577 100246577 100246577 TTGGCCAGCCATGTGGGTCCAGGCAACAGGTCATGGGCAGGGAGGCACAAGGGAAGACGTCATCG TTGGCCAGCCATGTGGGTCCAGGCAACAGGTCGTGGGCAGGGAGGCACAAGGGAAGACGTCATCG T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100246412..100246625 26863196 MeRIP-seq:(Medium) rs1346077737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93743,RMVar_hsa_circ_247084 74463 RMVar_ID_74463 Human_SNP_ID_332609170 m1A Human chr7 + 100272133 100272133 100272133 CGGACAAAAGGGAGGAGGCCCGCCAAGTTGCGAGGGGGAGCCACGGGTCGAGGGAGGCAGCGCCG CGGACAAAAGGGAGGAGGCCCGCCAAGTTGCGGGGGGGAGCCACGGGTCGAGGGAGGCAGCGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100272087..100272203 26863196 MeRIP-seq:(Medium) rs936306949 Functional Loss SNV dbSNP153 33..33 33 - - - 74464 RMVar_ID_74464 Human_SNP_ID_332625415 m1A Human chr7 - 100335899 100335899 100335899 GGAGGCGGGGCGCCTGTGGGAGCCGTGGAGGGAACTTTCCCAGTCCCCGAGGCGGATCCGGTGTT GGAGGCGGGGCGCCTGTGGGAGCCGTGGAGGGTACTTTCCCAGTCCCCGAGGCGGATCCGGTGTT T A PMS2P1 Ensembl:ENSG00000078319 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100335824..100335908 26863196 MeRIP-seq:(Medium) rs879393607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956531,Human_RBP_ID_8944277,Human_RBP_ID_9337265,Human_RBP_ID_9404740,Human_RBP_ID_17171216,Human_RBP_ID_17427870,Human_RBP_ID_22111008 Human_Splice_Rec_898597 Human_miRNA_ID_1899901 74465 RMVar_ID_74465 Human_SNP_ID_332625416 m1A Human chr7 - 100335899 100335899 100335899 GGAGGCGGGGCGCCTGTGGGAGCCGTGGAGGGAACTTTCCCAGTCCCCGAGGCGGATCCGGTGTT GGAGGCGGGGCGCCTGTGGGAGCCGTGGAGGGCACTTTCCCAGTCCCCGAGGCGGATCCGGTGTT T G PMS2P1 Ensembl:ENSG00000078319 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100335824..100335908 26863196 MeRIP-seq:(Medium) rs879393607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956531,Human_RBP_ID_8944277,Human_RBP_ID_9337265,Human_RBP_ID_9404740,Human_RBP_ID_17171216,Human_RBP_ID_17427870,Human_RBP_ID_22111008 Human_Splice_Rec_898597 Human_miRNA_ID_1899901 74466 RMVar_ID_74466 Human_SNP_ID_332625522 m1A Human chr7 - 100336177 100336153 100336177 GGGTGGCGCGTGCCAGACACCAACGGTCGGAAACCGCCAGACACCAACGCTCGGAATCCACGCCA GGGTGGCGCGTGCCAGACACCAACGGTCGGAA________________________TCCACGCCA ATTCCGAGCGTTGGTGTCTGGCGGT A PMS2P1 Ensembl:ENSG00000078319 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100336126..100336244 26863196 MeRIP-seq:(Medium) rs879252781 Functional Loss DEL dbSNP153 33..56 33 - - - 74467 RMVar_ID_74467 Human_SNP_ID_332630011 m1A Human chr7 - 100352474 100352474 100352474 CCTGCCCCTCTCTGGTGCCGGCACTCACCTGCAGTGACACGCAGGGTCAGCAGCACCCAGGGCAG CCTGCCCCTCTCTGGTGCCGGCACTCACCTGCGGTGACACGCAGGGTCAGCAGCACCCAGGGCAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:100352451..100352475;chr7:100352351..100352700 26863196 MeRIP-seq:(Medium) rs1308952887 Functional Loss SNV dbSNP153 33..33 33 - - - 74468 RMVar_ID_74468 Human_SNP_ID_332630338 m1A Human chr7 - 100353485 100353485 100353485 CCAGTGTGCGGTGTGGGTGGGGAGTGATGCCCACCAGGACGGCCCCCTGTCGGGGGTGAGCTGTG CCAGTGTGCGGTGTGGGTGGGGAGTGATGCCCCCCAGGACGGCCCCCTGTCGGGGGTGAGCTGTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100353482..100353594 32194978 MeRIP-seq:(Medium) rs2012561 Functional Loss SNV dbSNP153 33..33 33 - - - 74469 RMVar_ID_74469 Human_SNP_ID_332630410 m1A Human chr7 - 100353727 100353727 100353727 ACGTAAGGGGGTGGCACCCAGGAGGCCTGGGAAGGGGAAAGCCCAGTGGCCTCATGGTCTCTCTC ACGTAAGGGGGTGGCACCCAGGAGGCCTGGGAGGGGGAAAGCCCAGTGGCCTCATGGTCTCTCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100353680..100353830 32194978 MeRIP-seq:(Medium) rs1306433524 Functional Loss SNV dbSNP153 33..33 33 - - - 74470 RMVar_ID_74470 Human_SNP_ID_332630469 m1A Human chr7 + 100353924 100353909 100353924 CAGTCGTTTCCTGCTGTGACTAAGTCAGCAACACAGTTCCTCTGACATGGGCCTTGGCTGTGCTT CAGTCGTTTCCTGCTGTG_______________CAGTTCCTCTGACATGGGCCTTGGCTGTGCTT GACTAAGTCAGCAACA G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100353876..100353975 26863196 MeRIP-seq:(Medium) rs1173522155 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_2050481,Human_RBP_ID_3860182,Human_RBP_ID_5627971,Human_RBP_ID_16271700,Human_RBP_ID_18888834,Human_RBP_ID_22835901 Human_Splice_Rec_898677,Human_Splice_Rec_898734,Human_Splice_Rec_898735,Human_Splice_Rec_898763,Human_Splice_Rec_898773,Human_Splice_Rec_898820,Human_Splice_Rec_898821,Human_Splice_Rec_898838,Human_Splice_Rec_898839,Human_Splice_Rec_898855,Human_Splice_Rec_898866,Human_Splice_Rec_898867,Human_Splice_Rec_898873 RMVar_hsa_circ_2314,RMVar_hsa_circ_48532,RMVar_hsa_circ_93853,RMVar_hsa_circ_77737,RMVar_hsa_circ_247091,RMVar_hsa_circ_247092,RMVar_hsa_circ_64288,RMVar_hsa_circ_110177,RMVar_hsa_circ_99772,RMVar_hsa_circ_247093,RMVar_hsa_circ_123314,RMVar_hsa_circ_247094,RMVar_hsa_circ_247095 74471 RMVar_ID_74471 Human_SNP_ID_332630479 m1A Human chr7 - 100353950 100353950 100353950 CCTCCCCAATCTCTTCACCCCCAAAGAAGCACAGCCAAGGCCCATGTCAGAGGAACTGTGTTGCT CCTCCCCAATCTCTTCACCCCCAAAGAAGCACGGCCAAGGCCCATGTCAGAGGAACTGTGTTGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100353899..100354059 26863196 MeRIP-seq:(Medium) rs761160680 Functional Loss SNV dbSNP153 33..33 33 - - - 74472 RMVar_ID_74472 Human_SNP_ID_332630482 m1A Human chr7 - 100353956 100353956 100353956 AGACTTCCTCCCCAATCTCTTCACCCCCAAAGAAGCACAGCCAAGGCCCATGTCAGAGGAACTGT AGACTTCCTCCCCAATCTCTTCACCCCCAAAGCAGCACAGCCAAGGCCCATGTCAGAGGAACTGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100353822..100354045 26863196 MeRIP-seq:(Medium) rs974634613 Functional Loss SNV dbSNP153 33..33 33 - - - 74473 RMVar_ID_74473 Human_SNP_ID_332631367 m1A Human chr7 - 100357209 100357208 100357210 CAAGGGGTGAGGGGGCTGACGGTCCCCTACACAGAGACTGGTCCCTCTCGAGGCCACCCCTTGAC CAAGGGGTGAGGGGGCTGACGGTCCCCTACA__GAGACTGGTCCCTCTCGAGGCCACCCCTTGAC CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100357192..100357603 26863196 MeRIP-seq:(Medium) rs1254621732 Functional Loss DEL dbSNP153 32..33 33 - - - 74474 RMVar_ID_74474 Human_SNP_ID_332632140 m1A Human chr7 + 100359409 100359409 100359409 CACCATAGCCGGCCTCAGGGTCACAGAAAGCAAAGGGCACTCAGAATCATGGCACCTAAGTCTGG CACCATAGCCGGCCTCAGGGTCACAGAAAGCAGAGGGCACTCAGAATCATGGCACCTAAGTCTGG A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100359314..100359441 26863196 MeRIP-seq:(Medium) rs1256897163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628145,Human_RBP_ID_16271757,Human_RBP_ID_18888849 Human_Splice_Rec_898686,Human_Splice_Rec_898730,Human_Splice_Rec_898754,Human_Splice_Rec_898794,Human_Splice_Rec_898892 RMVar_hsa_circ_277057,RMVar_hsa_circ_247099,RMVar_hsa_circ_247100,RMVar_hsa_circ_87209,RMVar_hsa_circ_247102 74475 RMVar_ID_74475 Human_SNP_ID_332632874 m1A Human chr7 + 100362034 100362034 100362034 GATTCTAGCAGAAAATCAGATCAGGAGATCACAGAAGGTCAAGGAACTACTGAGAGAGCAGGAAT GATTCTAGCAGAAAATCAGATCAGGAGATCACGGAAGGTCAAGGAACTACTGAGAGAGCAGGAAT A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100362028..100362142 26863196 MeRIP-seq:(Medium) rs1354594995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14483,Human_RBP_ID_3867416,Human_RBP_ID_16271781 RMVar_hsa_circ_247100 74476 RMVar_ID_74476 Human_SNP_ID_332634371 m1A Human chr7 + 100367385 100367385 100367385 CAGGGCGCCAAGCAGTGACTTCTGACCAACAGAGTGTGGGGAGAAGGGATGTGTATTAGCCCCGG CAGGGCGCCAAGCAGTGACTTCTGACCAACAGTGTGTGGGGAGAAGGGATGTGTATTAGCCCCGG A T PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100359375..100367385 32194978 MeRIP-seq:(Medium) rs776729139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2050500,Human_RBP_ID_3867420,Human_RBP_ID_5105436,Human_RBP_ID_8675942,Human_RBP_ID_18171756,Human_RBP_ID_24235146 Human_Splice_Rec_898688,Human_Splice_Rec_898732,Human_Splice_Rec_898756,Human_Splice_Rec_898796,Human_Splice_Rec_898894 RMVar_hsa_circ_247100 74477 RMVar_ID_74477 Human_SNP_ID_332634433 m1A Human chr7 + 100367570 100367570 100367570 CCTGAATCACCGACTGGAGGAGAGTTACCTACAAGAGCCTTCATCCAGGAGCATCCACACTGCAA CCTGAATCACCGACTGGAGGAGAGTTACCTACGAGAGCCTTCATCCAGGAGCATCCACACTGCAA A G PILRA,PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000085514,Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,Protein coding,lincRNA 5'UTR,3'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100367461..100367675 26863196 MeRIP-seq:(Medium) rs1483062791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86555,Human_RBP_ID_691516,Human_RBP_ID_954712,Human_RBP_ID_2050503,Human_RBP_ID_3867421,Human_RBP_ID_3971105,Human_RBP_ID_5105396,Human_RBP_ID_5533636,Human_RBP_ID_5657897,Human_RBP_ID_16271835,Human_RBP_ID_18171756,Human_RBP_ID_18888867,Human_RBP_ID_19019928,Human_RBP_ID_21993877,Human_RBP_ID_26356804 Human_Splice_Rec_898903 RMVar_hsa_circ_247100 74478 RMVar_ID_74478 Human_SNP_ID_332636496 m1A Human chr7 + 100375090 100375090 100375090 ATCATATCCCTCTCTTCCTGCATCCATCCTTTACCCTCCTCACTTCTCCCTGGCCCCTGCAGCCC ATCATATCCCTCTCTTCCTGCATCCATCCTTTGCCCTCCTCACTTCTCCCTGGCCCCTGCAGCCC A G PILRA Ensembl:ENSG00000085514 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100375041..100375131 26863196 MeRIP-seq:(Medium) rs573612666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21553886 74479 RMVar_ID_74479 Human_SNP_ID_332650033 m1A Human chr7 - 100428849 100428849 100428849 CTCTCCGCCTCAACACCCACGACCCGAACCCCAACGCATCCGCCCACTCCCGACGCCCGCTCACT CTCTCCGCCTCAACACCCACGACCCGAACCCCGACGCATCCGCCCACTCCCGACGCCCGCTCACT T C ZCWPW1 Ensembl:ENSG00000078487 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:100428801..100428992;chr7:100428793..100429122 26863196 MeRIP-seq:(Medium) rs1335625157 Functional Loss SNV dbSNP153 33..33 33 - - - 74480 RMVar_ID_74480 Human_SNP_ID_332650384 m1A Human chr7 - 100429510 100429510 100429510 CTTTGTCTCTGCCGCGCGATCCCACCCACCGTAGGCGGGGGACGGGAGCTGGTGTGAAAAGGTCT CTTTGTCTCTGCCGCGCGATCCCACCCACCGTGGGCGGGGGACGGGAGCTGGTGTGAAAAGGTCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:100429426..100429625 26863196 MeRIP-seq:(Medium) rs1187791755 Functional Loss SNV dbSNP153 33..33 33 - - - 74481 RMVar_ID_74481 Human_SNP_ID_332650518 m1A Human chr7 - 100429784 100429784 100429784 AACTACTCGAGGACTCAACCGCGCGTGCGCCGACCCCTTTCTCCTCCGCCACTACCACCCGGCCG AACTACTCGAGGACTCAACCGCGCGTGCGCCGCCCCCTTTCTCCTCCGCCACTACCACCCGGCCG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:100429401..100429975 26863196 MeRIP-seq:(Medium) rs1050843799 Functional Loss SNV dbSNP153 33..33 33 - - - 74482 RMVar_ID_74482 Human_SNP_ID_332650574 m1A Human chr7 + 100429908 100429908 100429908 GGCGCTTGGGCGCGAGACTAGGCGTGAAGAGCAGAGCTGCGCGCGCACTCGGGAAAGGGGGGAAG GGCGCTTGGGCGCGAGACTAGGCGTGAAGAGCTGAGCTGCGCGCGCACTCGGGAAAGGGGGGAAG A T MEPCE Ensembl:ENSG00000146834 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:100429398..100430638;chr7:100429315..100431266;chr7:100428801..100431060 26863196 MeRIP-seq:(Medium) rs1387180561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671405,Human_RBP_ID_4958265,Human_RBP_ID_7666287,Human_RBP_ID_17166962 74483 RMVar_ID_74483 Human_SNP_ID_332650973 m1A Human chr7 - 100430861 100430861 100430861 GGGGTGAGAGGGGCTGTGGGCGGCACGGGGTGACTCTCACTCCCTCCGGCTGCCTGCTGCTGCTG GGGGTGAGAGGGGCTGTGGGCGGCACGGGGTGGCTCTCACTCCCTCCGGCTGCCTGCTGCTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100430811..100431051 26863196 MeRIP-seq:(Medium) rs6962151 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 74484 RMVar_ID_74484 Human_SNP_ID_332652918 m1A Human chr7 + 100435991 100435991 100435991 GGCCCAAGGCCAGGCTGCTCTTCAGCACGGGCATCTCCAGCTCCTGCGGCACCGCAGGCTGCGGC GGCCCAAGGCCAGGCTGCTCTTCAGCACGGGCGTCTCCAGCTCCTGCGGCACCGCAGGCTGCGGC A G AC092849.1 Ensembl:ENSG00000241357 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100435634..100436162 26863196 MeRIP-seq:(Medium) rs1190907223 Functional Loss SNV dbSNP153 33..33 33 - - - 74485 RMVar_ID_74485 Human_SNP_ID_332653061 m1A Human chr7 - 100436259 100436253 100436259 CCAAGTCCCGCAACTCCGAGCCCCAGTGCCCGAGCCCGGCCTGGACTTGAGCCTGAGCCCGCGGC CCAAGTCCCGCAACTCCGAGCCCCAGTGCCCG______GCCTGGACTTGAGCCTGAGCCCGCGGC CCGGGCT C PPP1R35 Ensembl:ENSG00000160813 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100436213..100436450 26863196 MeRIP-seq:(Medium) rs1372132958 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_27350169 RMVar_hsa_circ_106205,RMVar_hsa_circ_247104 74486 RMVar_ID_74486 Human_SNP_ID_332653092 m1A Human chr7 + 100436313 100436313 100436313 GCGGGACTTGGGGCTCCGGGGGTGGCCCCGGGACCGCCGCGGCTTCTTCCCCGTCCGCCGACTTC GCGGGACTTGGGGCTCCGGGGGTGGCCCCGGGGCCGCCGCGGCTTCTTCCCCGTCCGCCGACTTC A G AC092849.1,PPP1R35-AS1 Ensembl:ENSG00000241357,Ensembl:ENSG00000240211 lincRNA,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:100435926..100436425 26863196 MeRIP-seq:(Medium) rs1346154864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868036,Human_RBP_ID_4917286,Human_RBP_ID_8220881 Human_Splice_Rec_899137 74487 RMVar_ID_74487 Human_SNP_ID_332653148 m1A Human chr7 - 100436421 100436421 100436421 GCGGCAGCCAGGCTGTGTCCCCTGACCGTTGGAGCGTCTGCGACCCCCGCATCCCCGCACCCTCA GCGGCAGCCAGGCTGTGTCCCCTGACCGTTGGCGCGTCTGCGACCCCCGCATCCCCGCACCCTCA T G PPP1R35 Ensembl:ENSG00000160813 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100436176..100436475 26863196 MeRIP-seq:(Medium) rs1389493064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1679398,Human_RBP_ID_4956534,Human_RBP_ID_5123057,Human_RBP_ID_18171757,Human_RBP_ID_18426066,Human_RBP_ID_23080364 RMVar_hsa_circ_106205,RMVar_hsa_circ_247104 74488 RMVar_ID_74488 Human_SNP_ID_332664123 m1A Human chr7 - 100477850 100477850 100477850 GGGGGCAAGGGCACCCCCCGGAATGGCTCCCCACCACCTGGGGCCCCTTCCTCCCGTTTCCGGGT GGGGGCAAGGGCACCCCCCGGAATGGCTCCCCCCCACCTGGGGCCCCTTCCTCCCGTTTCCGGGT T G TSC22D4 Ensembl:ENSG00000166925 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100477752..100477902 26863410 MeRIP-seq:(Medium) rs556683904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337905,Human_RBP_ID_18087243,Human_RBP_ID_22534261,Human_RBP_ID_27527220 74489 RMVar_ID_74489 Human_SNP_ID_332664213 m1A Human chr7 - 100478038 100478038 100478038 CAACCTTGGCCCAGCCCTGAGCCCCAGGGACCATGAGCGGGGGCAAGAAGAAGAGTAGTTTCCAA CAACCTTGGCCCAGCCCTGAGCCCCAGGGACCGTGAGCGGGGGCAAGAAGAAGAGTAGTTTCCAA T C TSC22D4 Ensembl:ENSG00000166925 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100477987..100478299 26863196 MeRIP-seq:(Medium) rs1403478578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87484,Human_RBP_ID_216547,Human_RBP_ID_4917345,Human_RBP_ID_5134584,Human_RBP_ID_9439321,Human_RBP_ID_17092651,Human_RBP_ID_22112628,Human_RBP_ID_27842933 74490 RMVar_ID_74490 Human_SNP_ID_332664263 m1A Human chr7 - 100478149 100478149 100478149 GCCCTCCTGCCATGTCGGACCCAGACGTCCCCAGGGGCTCGGATGTCCCCGCCATGTGGCCCCCT GCCCTCCTGCCATGTCGGACCCAGACGTCCCCCGGGGCTCGGATGTCCCCGCCATGTGGCCCCCT T G TSC22D4 Ensembl:ENSG00000166925 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100478099..100478199 32194978 MeRIP-seq:(Medium) rs1348557805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_216548,Human_RBP_ID_5134585,Human_RBP_ID_5152995,Human_RBP_ID_17092386,Human_RBP_ID_17427388,Human_RBP_ID_18960249 74491 RMVar_ID_74491 Human_SNP_ID_332666031 m1A Human chr7 - 100484267 100484267 100484267 CTCCATACCTGCTCCGGTTTTCCTTCCCCCAAACCCACACTCTTCTTTTCGCCTTCAGCCTCACT CTCCATACCTGCTCCGGTTTTCCTTCCCCCAATCCCACACTCTTCTTTTCGCCTTCAGCCTCACT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100484235..100484319 26863196 MeRIP-seq:(Medium) rs937336381 Functional Loss SNV dbSNP153 33..33 33 - - - 74492 RMVar_ID_74492 Human_SNP_ID_332681072 m1A Human chr7 - 100539351 100539351 100539351 CGCCCGGGCCCGGGCCCTTCTTCGCCGCCATCACCATCGCTGCCCACTCCCTCCCCGCTAGTCAG CGCCCGGGCCCGGGCCCTTCTTCGCCGCCATCGCCATCGCTGCCCACTCCCTCCCCGCTAGTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100539203..100548913 26863196 MeRIP-seq:(Medium) rs1266147524 Functional Loss SNV dbSNP153 33..33 33 - - - 74493 RMVar_ID_74493 Human_SNP_ID_332681212 m1A Human chr7 + 100539746 100539746 100539746 TCGTCTGCTGCAGCGGTGTGGTGGGGAGGGGAAAGGGCAGGGGAGAGGAAGCAAGGCCGGAGTCG TCGTCTGCTGCAGCGGTGTGGTGGGGAGGGGAGAGGGCAGGGGAGAGGAAGCAAGGCCGGAGTCG A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100539742..100539852 26863196 MeRIP-seq:(Medium) rs999784432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267849,Human_RBP_ID_844059,Human_RBP_ID_3862534,Human_RBP_ID_5220498,Human_RBP_ID_8218451,Human_RBP_ID_9438956,Human_RBP_ID_17200133,Human_RBP_ID_18959455,Human_RBP_ID_22731210,Human_RBP_ID_23297432 RMVar_hsa_circ_247109,RMVar_hsa_circ_103660 74494 RMVar_ID_74494 Human_SNP_ID_332687388 m1A Human chr7 + 100564943 100564943 100564943 TGTATTGTTCTTTCTTTCCAGACTGGACCCTCATCAAGCCCATTCGCCTCCAAACCTCCAACCAC TGTATTGTTCTTTCTTTCCAGACTGGACCCTCGTCAAGCCCATTCGCCTCCAAACCTCCAACCAC A G AGFG2 Ensembl:ENSG00000106351 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100563949..100565032 26863196 MeRIP-seq:(Medium) rs199744807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8652556 Human_Splice_Rec_899244,Human_Splice_Rec_899278,Human_Splice_Rec_899292 74495 RMVar_ID_74495 Human_SNP_ID_332690043 m1A Human chr7 - 100573638 100573638 100573638 GGCAAGGACCAGGGCGAGCCCTGGAGCGCCGGAGCGGACGCCCCCAGGGAGCTGGGGACACCCCC GGCAAGGACCAGGGCGAGCCCTGGAGCGCCGGTGCGGACGCCCCCAGGGAGCTGGGGACACCCCC T A SAP25,AC069281.2 Ensembl:ENSG00000205307,Ensembl:ENSG00000274272 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100573588..100573992 26863196 MeRIP-seq:(Medium) rs1333078700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267851,Human_RBP_ID_3971108,Human_RBP_ID_5152996,Human_RBP_ID_5243054,Human_RBP_ID_5327948,Human_RBP_ID_8149577,Human_RBP_ID_19139092,Human_RBP_ID_21992952,Human_RBP_ID_22483323,Human_RBP_ID_23080110 Human_Splice_Rec_899293,Human_Splice_Rec_899303 74496 RMVar_ID_74496 Human_SNP_ID_332690215 m1A Human chr7 + 100574111 100574111 100574111 CCCGCGGTCCTTCCACCCAGACCCTCGACCCCAGAGGCAGCCAGGCCGGCAGGCCAAGGGTGCCC CCCGCGGTCCTTCCACCCAGACCCTCGACCCCGGAGGCAGCCAGGCCGGCAGGCCAAGGGTGCCC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100574060..100574328 32194978 MeRIP-seq:(Medium) rs1045141822 Functional Loss SNV dbSNP153 33..33 33 - - - 74497 RMVar_ID_74497 Human_SNP_ID_332690312 m1A Human chr7 + 100574347 100574345 100574347 CCCCTCCTCTTCCAGGATGTGGTGGGGCTGGCACAGTGACTCCTGGGGGAAGGGGCCGGGTTAGC CCCCTCCTCTTCCAGGATGTGGTGGGGCTGG__CAGTGACTCCTGGGGGAAGGGGCCGGGTTAGC GCA G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100574110..100574713 26863196 MeRIP-seq:(Medium) rs1295814153 Functional Loss DEL dbSNP153 32..33 33 - - - 74498 RMVar_ID_74498 Human_SNP_ID_332690412 m1A Human chr7 + 100574618 100574617 100574619 GCCATGGCCACAGCCACCAACACGCGGAGCAGACGCGCGCGCGCGCGCACACACACACACACAGG GCCATGGCCACAGCCACCAACACGCGGAGCAG__GCGCGCGCGCGCGCACACACACACACACAGG GAC G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100574575..100574773 32194978 MeRIP-seq:(Medium) rs1562803001 Functional Loss DEL dbSNP153 33..34 33 - - - 74499 RMVar_ID_74499 Human_SNP_ID_332690413 m1A Human chr7 + 100574618 100574618 100574618 GCCATGGCCACAGCCACCAACACGCGGAGCAGACGCGCGCGCGCGCGCACACACACACACACAGG GCCATGGCCACAGCCACCAACACGCGGAGCAGGCGCGCGCGCGCGCGCACACACACACACACAGG A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100574575..100574773 32194978 MeRIP-seq:(Medium) rs529166555 Functional Loss SNV dbSNP153 33..33 33 - - - 74500 RMVar_ID_74500 Human_SNP_ID_332691784 m1A Human chr7 - 100577369 100577369 100577369 TTGGTCCCTCAGGCGGGAGGAGCCGGCAGGGGAGGAGCGGCGGCGCCCGGACACCTTGCAGCTGT TTGGTCCCTCAGGCGGGAGGAGCCGGCAGGGGTGGAGCGGCGGCGCCCGGACACCTTGCAGCTGT T A AC069281.2,LRCH4 Ensembl:ENSG00000274272,Ensembl:ENSG00000077454 lincRNA,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100577009..100577699;chr7:100577001..100577509 26863196 MeRIP-seq:(Medium) rs1562805727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253998,Human_RBP_ID_794227,Human_RBP_ID_842899,Human_RBP_ID_954723,Human_RBP_ID_3971126,Human_RBP_ID_5153007,Human_RBP_ID_5220066,Human_RBP_ID_5328550,Human_RBP_ID_5657927,Human_RBP_ID_18472354,Human_RBP_ID_19019946,Human_RBP_ID_19135256,Human_RBP_ID_22687129,Human_RBP_ID_23215581,Human_RBP_ID_26132122,Human_RBP_ID_26356812,Human_RBP_ID_27829603 Human_Splice_Rec_899334,Human_Splice_Rec_899335,Human_Splice_Rec_899382,Human_Splice_Rec_899383,Human_Splice_Rec_899402,Human_Splice_Rec_899430,Human_Splice_Rec_899431,Human_Splice_Rec_899468,Human_Splice_Rec_899469 74501 RMVar_ID_74501 Human_SNP_ID_332692028 m1A Human chr7 - 100577879 100577879 100577879 CAACAGATGAATTTTCAGAGCTGTCATTCCGGATCTCAGAGCTGGCCCGGGAGCCCCGGGGACCC CAACAGATGAATTTTCAGAGCTGTCATTCCGGTTCTCAGAGCTGGCCCGGGAGCCCCGGGGACCC T A AC069281.2,LRCH4 Ensembl:ENSG00000274272,Ensembl:ENSG00000077454 lincRNA,Protein coding exon,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100577829..100578175 32194978 MeRIP-seq:(Medium) rs1562806219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105285,Human_RBP_ID_5627755,Human_RBP_ID_22514888,Human_RBP_ID_23080112 Human_Splice_Rec_899328,Human_Splice_Rec_899329,Human_Splice_Rec_899376,Human_Splice_Rec_899377,Human_Splice_Rec_899397,Human_Splice_Rec_899424,Human_Splice_Rec_899425,Human_Splice_Rec_899462,Human_Splice_Rec_899463,Human_Splice_Rec_899487 RMVar_hsa_circ_378396 74502 RMVar_ID_74502 Human_SNP_ID_332692350 m1A Human chr7 - 100578788 100578788 100578788 TGTTCCTGACTTTTCCCTTGCCCACCTGTTCCAGAGCTGGGGGACCTCCCTCTGGTCCGCCTGGA TGTTCCTGACTTTTCCCTTGCCCACCTGTTCCGGAGCTGGGGGACCTCCCTCTGGTCCGCCTGGA T C LRCH4 Ensembl:ENSG00000077454 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100578754..100578905 32194978 MeRIP-seq:(Medium) rs371264894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794817,Human_RBP_ID_953296 RMVar_hsa_circ_13760,RMVar_hsa_circ_310744 74503 RMVar_ID_74503 Human_SNP_ID_332692881 m1A Human chr7 + 100580464 100580464 100580464 ACACACACACACACAAAACCCACACACACGCAAACAACATACATACACACAGACACAAACAACAT ACACACACACACACAAAACCCACACACACGCACACAACATACATACACACAGACACAAACAACAT A C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100580462..100580810 26863196 MeRIP-seq:(Medium) rs931731931 Functional Loss SNV dbSNP153 33..33 33 - - - 74504 RMVar_ID_74504 Human_SNP_ID_332692902 m1A Human chr7 + 100580502 100580501 100580503 ATACATACACACAGACACAAACAACATGCACAACACACACATAAACATACACAACACATACACAC ATACATACACACAGACACAAACAACATGCACA__ACACACATAAACATACACAACACATACACAC AAC A RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100580492..100580725 26863196 MeRIP-seq:(Medium) rs1262451328 Functional Loss DEL dbSNP153 33..34 33 - - - 74505 RMVar_ID_74505 Human_SNP_ID_332694779 m1A Human chr7 + 100586062 100586062 100586062 CCGGGCACGGAGGTCGTGGCTGCCGCCTCCTCACCCCCGGCGGCGAGTGGAGCCGCTACGGCCGC CCGGGCACGGAGGTCGTGGCTGCCGCCTCCTCCCCCCCGGCGGCGAGTGGAGCCGCTACGGCCGC A C FBXO24 Ensembl:ENSG00000106336 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100585973..100586119 26863196 MeRIP-seq:(Medium) rs746418640 Functional Loss SNV dbSNP153 33..33 33 - - - 74506 RMVar_ID_74506 Human_SNP_ID_332694790 m1A Human chr7 - 100586077 100586077 100586077 CGGGAGCGGATGGCGGCGGCCGTAGCGGCTCCACTCGCCGCCGGGGGTGAGGAGGCGGCAGCCAC CGGGAGCGGATGGCGGCGGCCGTAGCGGCTCCGCTCGCCGCCGGGGGTGAGGAGGCGGCAGCCAC T C LRCH4 Ensembl:ENSG00000077454 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100585976..100586114 26863410 MeRIP-seq:(Medium) rs1054408139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794818,Human_RBP_ID_4917444,Human_RBP_ID_27830583 74507 RMVar_ID_74507 Human_SNP_ID_332694791 m1A Human chr7 - 100586077 100586077 100586077 CGGGAGCGGATGGCGGCGGCCGTAGCGGCTCCACTCGCCGCCGGGGGTGAGGAGGCGGCAGCCAC CGGGAGCGGATGGCGGCGGCCGTAGCGGCTCCCCTCGCCGCCGGGGGTGAGGAGGCGGCAGCCAC T G LRCH4 Ensembl:ENSG00000077454 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100585976..100586114 26863410 MeRIP-seq:(Medium) rs1054408139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794818,Human_RBP_ID_4917444,Human_RBP_ID_27830583 74508 RMVar_ID_74508 Human_SNP_ID_332694808 m1A Human chr7 + 100586099 100586099 100586099 CGGCGGCGAGTGGAGCCGCTACGGCCGCCGCCATCCGCTCCCGGCGGCTCCCGCTGCCTGACTGA CGGCGGCGAGTGGAGCCGCTACGGCCGCCGCCCTCCGCTCCCGGCGGCTCCCGCTGCCTGACTGA A C FBXO24 Ensembl:ENSG00000106336 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100585934..100586150 26863196 MeRIP-seq:(Medium) rs1468424426 Functional Loss SNV dbSNP153 33..33 33 - - - 74509 RMVar_ID_74509 Human_SNP_ID_332699854 m1A Human chr7 - 100604156 100604156 100604156 CAGAGCAGGAAGCCTCGTCCTCCTGTGCCCTCATCCGTCGTCATCCTCAGGGTCACCTGGTTGCC CAGAGCAGGAAGCCTCGTCCTCCTGTGCCCTCCTCCGTCGTCATCCTCAGGGTCACCTGGTTGCC T G PCOLCE-AS1 Ensembl:ENSG00000224729 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100603977..100604263 26863196 MeRIP-seq:(Medium) rs759556507 Functional Loss SNV dbSNP153 33..33 33 - - - 74510 RMVar_ID_74510 Human_SNP_ID_332700087 m1A Human chr7 - 100604790 100604790 100604790 CCGACCCGCGGCCGCACCGCGCCTCTTCCCCTAGGAGATCCCATCTCCCCGGCCCTGCAGCAGAG CCGACCCGCGGCCGCACCGCGCCTCTTCCCCTGGGAGATCCCATCTCCCCGGCCCTGCAGCAGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100604783..100605226 26863196 MeRIP-seq:(Medium) rs527701650 Functional Loss SNV dbSNP153 33..33 33 - - - 74511 RMVar_ID_74511 Human_SNP_ID_332700188 m1A Human chr7 + 100605098 100605098 100605098 CCCCGCTCCTCTCTCCCCTCCCCAGAGCACCAATTTTGCGGGGGGCGGCTGGAGAAGGCCCAGGG CCCCGCTCCTCTCTCCCCTCCCCAGAGCACCAGTTTTGCGGGGGGCGGCTGGAGAAGGCCCAGGG A G PCOLCE Ensembl:ENSG00000106333 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100604969..100605251 26863196 MeRIP-seq:(Medium) rs766639817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793111,Human_RBP_ID_22775013 Human_Splice_Rec_899624,Human_Splice_Rec_899644,Human_Splice_Rec_899646,Human_Splice_Rec_899648 Human_miRNA_ID_2973371,Human_miRNA_ID_3006557,Human_miRNA_ID_3010468 RMVar_hsa_circ_82548,RMVar_hsa_circ_95762,RMVar_hsa_circ_247121,RMVar_hsa_circ_99552,RMVar_hsa_circ_247122,RMVar_hsa_circ_247123 74512 RMVar_ID_74512 Human_SNP_ID_332700466 m1A Human chr7 + 100605846 100605846 100605846 TGAGGGGCGGGACCTGGGCGAGTCCGGGAGAGAGTCGGCGGACCGCACGCACGCGGCTGTTTGGA TGAGGGGCGGGACCTGGGCGAGTCCGGGAGAGGGTCGGCGGACCGCACGCACGCGGCTGTTTGGA A G PCOLCE Ensembl:ENSG00000106333 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100605748..100606047 26863196 MeRIP-seq:(Medium) rs755177400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82548,RMVar_hsa_circ_95762,RMVar_hsa_circ_247121,RMVar_hsa_circ_99552,RMVar_hsa_circ_247122,RMVar_hsa_circ_91338,RMVar_hsa_circ_247123,RMVar_hsa_circ_247124 74513 RMVar_ID_74513 Human_SNP_ID_332700515 m1A Human chr7 - 100605995 100605995 100605995 TCCCAACTTCGCAGAGCCCCAGTCGCCTCTCTATCCGCGGACCCCAGACCCGGGGCCAAATCTCC TCCCAACTTCGCAGAGCCCCAGTCGCCTCTCTGTCCGCGGACCCCAGACCCGGGGCCAAATCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100605519..100606087 26863196 MeRIP-seq:(Medium) rs945342022 Functional Loss SNV dbSNP153 33..33 33 - - - 74514 RMVar_ID_74514 Human_SNP_ID_332700716 m1A Human chr7 + 100606601 100606601 100606601 AGTCAAGCTGCCCCCCAAGTCCCAACCTCCGGAGAAAACAGAGGAATCTCCTTCAGCCCCTGGTG AGTCAAGCTGCCCCCCAAGTCCCAACCTCCGGGGAAAACAGAGGAATCTCCTTCAGCCCCTGGTG A G PCOLCE Ensembl:ENSG00000106333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100606454..100606614 26863196 MeRIP-seq:(Medium) rs922260284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956677 Human_Splice_Rec_899629,Human_Splice_Rec_899657,Human_Splice_Rec_899661 RMVar_hsa_circ_81891,RMVar_hsa_circ_82548,RMVar_hsa_circ_95762,RMVar_hsa_circ_247121,RMVar_hsa_circ_99552,RMVar_hsa_circ_247122,RMVar_hsa_circ_91338,RMVar_hsa_circ_247123,RMVar_hsa_circ_247124,RMVar_hsa_circ_247125 74515 RMVar_ID_74515 Human_SNP_ID_332708623 m1A Human chr7 - 100633666 100633666 100633666 GCGTCCGCGGGGAGCGCTCTTTTCCTAAACTCAGGAACCCCTCGCCGCCCCTGCCCCTGGCGACC GCGTCCGCGGGGAGCGCTCTTTTCCTAAACTCGGGAACCCCTCGCCGCCCCTGCCCCTGGCGACC T C TFR2 Ensembl:ENSG00000106327 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100633615..100633688 26863196 MeRIP-seq:(Medium) rs1261343016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265333 74516 RMVar_ID_74516 Human_SNP_ID_332719449 m1A Human chr7 - 100673620 100673620 100673620 CGAGGGAGCAAAGACGGGCCCAGTCGCTCCCAAGGTTCTCACCCTACGCTTTGTGGACGCAAACC CGAGGGAGCAAAGACGGGCCCAGTCGCTCCCAGGGTTCTCACCCTACGCTTTGTGGACGCAAACC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100673569..100673675 26863196 MeRIP-seq:(Medium) rs1316980969 Functional Loss SNV dbSNP153 33..33 33 - - - 74517 RMVar_ID_74517 Human_SNP_ID_332719654 m1A Human chr7 + 100673895 100673895 100673895 AGGAAGACAGCGCCGCCCGCGCACCGCCAGCGACCTCCGCCGCAGAGTCCCACCGCCACAGGTAC AGGAAGACAGCGCCGCCCGCGCACCGCCAGCGCCCTCCGCCGCAGAGTCCCACCGCCACAGGTAC A C GNB2 Ensembl:ENSG00000172354 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100673851..100674023 26863196 MeRIP-seq:(Medium) rs899622489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794500,Human_RBP_ID_4917500,Human_RBP_ID_22534333,Human_RBP_ID_26541524 Human_Splice_Rec_900035,Human_Splice_Rec_900053,Human_Splice_Rec_900069,Human_Splice_Rec_900085,Human_Splice_Rec_900097 74518 RMVar_ID_74518 Human_SNP_ID_332719664 m1A Human chr7 + 100673906 100673905 100673907 GCCGCCCGCGCACCGCCAGCGACCTCCGCCGCAGAGTCCCACCGCCACAGGTACCTTCGCTGGCA GCCGCCCGCGCACCGCCAGCGACCTCCGCCGC__AGTCCCACCGCCACAGGTACCTTCGCTGGCA CAG C GNB2 Ensembl:ENSG00000172354 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:100673751..100675287 26863410 MeRIP-seq:(Medium) rs1562856547 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_794500,Human_RBP_ID_4955912,Human_RBP_ID_22534333,Human_RBP_ID_26541524 Human_Splice_Rec_900035,Human_Splice_Rec_900053,Human_Splice_Rec_900069,Human_Splice_Rec_900085,Human_Splice_Rec_900097 74519 RMVar_ID_74519 Human_SNP_ID_332719667 m1A Human chr7 + 100673906 100673906 100673906 GCCGCCCGCGCACCGCCAGCGACCTCCGCCGCAGAGTCCCACCGCCACAGGTACCTTCGCTGGCA GCCGCCCGCGCACCGCCAGCGACCTCCGCCGCGGAGTCCCACCGCCACAGGTACCTTCGCTGGCA A G GNB2 Ensembl:ENSG00000172354 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:100673751..100675287 26863410 MeRIP-seq:(Medium) rs1053480842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794500,Human_RBP_ID_4955912,Human_RBP_ID_22534333,Human_RBP_ID_26541524 Human_Splice_Rec_900035,Human_Splice_Rec_900053,Human_Splice_Rec_900069,Human_Splice_Rec_900085,Human_Splice_Rec_900097 74520 RMVar_ID_74520 Human_SNP_ID_332720446 m1A Human chr7 + 100676187 100676187 100676187 ACGTCAGCCCTGCATCCCCCAGGCCTCGGGCCAGCGGCCAGGAGCTGCCTCCCCCAGCCCCCGTC ACGTCAGCCCTGCATCCCCCAGGCCTCGGGCCGGCGGCCAGGAGCTGCCTCCCCCAGCCCCCGTC A G GNB2 Ensembl:ENSG00000172354 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100676176..100676250 26863196 MeRIP-seq:(Medium) rs1048507942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795152,Human_RBP_ID_4955913,Human_RBP_ID_5429871,Human_RBP_ID_5451661,Human_RBP_ID_5478882,Human_RBP_ID_22463671 Human_Splice_Rec_900020,Human_Splice_Rec_900036,Human_Splice_Rec_900108,Human_Splice_Rec_900126 Human_miRNA_ID_694652,Human_miRNA_ID_1018214,Human_miRNA_ID_1037343,Human_miRNA_ID_1304680 74521 RMVar_ID_74521 Human_SNP_ID_332720616 m1A Human chr7 + 100676561 100676561 100676561 TTACAGGATGCCCGAAAAGCATGTGGGGACTCAACACTGACCCAGGTGAGGGCACTTGGTGGCCA TTACAGGATGCCCGAAAAGCATGTGGGGACTCGACACTGACCCAGGTGAGGGCACTTGGTGGCCA A G GNB2 Ensembl:ENSG00000172354 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100676176..100676862 32194978 MeRIP-seq:(Medium) rs1382685409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956548,Human_RBP_ID_19135272 Human_Splice_Rec_900022,Human_Splice_Rec_900023,Human_Splice_Rec_900038,Human_Splice_Rec_900039,Human_Splice_Rec_900054,Human_Splice_Rec_900055,Human_Splice_Rec_900070,Human_Splice_Rec_900071,Human_Splice_Rec_900110,Human_Splice_Rec_900111,Human_Splice_Rec_900128,Human_Splice_Rec_900129,Human_Splice_Rec_900140,Human_Splice_Rec_900141,Human_Splice_Rec_900150,Human_Splice_Rec_900151,Human_Splice_Rec_900166,Human_Splice_Rec_900167 74522 RMVar_ID_74522 Human_SNP_ID_332721059 m1A Human chr7 - 100677659 100677659 100677659 AAAAGGGCCCGAACTGGGCCAGGCCCCTCACCAGTGTGGCCAGGCAGCTCCCGGCTGACCCTGAC AAAAGGGCCCGAACTGGGCCAGGCCCCTCACCGGTGTGGCCAGGCAGCTCCCGGCTGACCCTGAC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100677647..100677745 26863196 MeRIP-seq:(Medium) rs1348604474 Functional Loss SNV dbSNP153 33..33 33 - - - 74523 RMVar_ID_74523 Human_SNP_ID_332721386 m1A Human chr7 - 100678379 100678379 100678379 CCGTTGGGGAAGAACTGCAGGACACGGGACCCAGATGGGGTGAGGGTGAGGGTGAGGAGCAGGGC CCGTTGGGGAAGAACTGCAGGACACGGGACCCGGATGGGGTGAGGGTGAGGGTGAGGAGCAGGGC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100678376..100678450 26863196 MeRIP-seq:(Medium) rs1206236257 Functional Loss SNV dbSNP153 33..33 33 - - - 74524 RMVar_ID_74524 Human_SNP_ID_332721457 m1A Human chr7 + 100678544 100678544 100678544 GGCATCACCTCTGTTGCCTTCTCGCGCAGCGGACGGCTGCTGCTCGCTGGCTACGACGACTTCAA GGCATCACCTCTGTTGCCTTCTCGCGCAGCGGGCGGCTGCTGCTCGCTGGCTACGACGACTTCAA A G GNB2 Ensembl:ENSG00000172354 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100678397..100678564 26863196 MeRIP-seq:(Medium) rs1358828304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671495,Human_RBP_ID_5478883,Human_RBP_ID_8652598,Human_RBP_ID_26830633 Human_Splice_Rec_900051,Human_Splice_Rec_900067,Human_Splice_Rec_900083,Human_Splice_Rec_900095,Human_Splice_Rec_900105,Human_Splice_Rec_900123,Human_Splice_Rec_900163,Human_Splice_Rec_900179,Human_Splice_Rec_900187 Human_miRNA_ID_2099609,Human_miRNA_ID_2105564,Human_miRNA_ID_2111507,Human_miRNA_ID_2164054,Human_miRNA_ID_2595279,Human_miRNA_ID_2738224,Human_miRNA_ID_3038822 RMVar_hsa_circ_98394,RMVar_hsa_circ_115909,RMVar_hsa_circ_105551,RMVar_hsa_circ_247136,RMVar_hsa_circ_114407,RMVar_hsa_circ_247137,RMVar_hsa_circ_247138,RMVar_hsa_circ_247139 74525 RMVar_ID_74525 Human_SNP_ID_332722024 m1A Human chr7 - 100679607 100679607 100679607 GGGTCACCGTGTTCCCTGTCTGCCTTGTACCCACAGTCTCCCCGCCCCCTCTCCACCCTGTGTGA GGGTCACCGTGTTCCCTGTCTGCCTTGTACCCTCAGTCTCCCCGCCCCCTCTCCACCCTGTGTGA T A GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100679558..100679695 26863196 MeRIP-seq:(Medium) rs545763341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123066,Human_RBP_ID_15945387,Human_RBP_ID_17092396,Human_RBP_ID_18960261,Human_RBP_ID_24180152 Human_miRNA_ID_2146467,Human_miRNA_ID_2386683,Human_miRNA_ID_2388157,Human_miRNA_ID_2399310,Human_miRNA_ID_2987891,Human_miRNA_ID_3021590,Human_miRNA_ID_3030360,Human_miRNA_ID_3085918 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74526 RMVar_ID_74526 Human_SNP_ID_332722025 m1A Human chr7 - 100679607 100679607 100679607 GGGTCACCGTGTTCCCTGTCTGCCTTGTACCCACAGTCTCCCCGCCCCCTCTCCACCCTGTGTGA GGGTCACCGTGTTCCCTGTCTGCCTTGTACCCCCAGTCTCCCCGCCCCCTCTCCACCCTGTGTGA T G GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100679558..100679695 26863196 MeRIP-seq:(Medium) rs545763341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123066,Human_RBP_ID_15945387,Human_RBP_ID_17092396,Human_RBP_ID_18960261,Human_RBP_ID_24180152 Human_miRNA_ID_2146467,Human_miRNA_ID_2386683,Human_miRNA_ID_2388157,Human_miRNA_ID_2399310,Human_miRNA_ID_2987891,Human_miRNA_ID_3021590,Human_miRNA_ID_3030360,Human_miRNA_ID_3085918 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74527 RMVar_ID_74527 Human_SNP_ID_332722105 m1A Human chr7 - 100679789 100679789 100679789 CCTGTGAGGAAGTATAGGGGGAGCCCTCTCCCACCCCCATCCCCTTCTGAGAGTGGTCAATGTTT CCTGTGAGGAAGTATAGGGGGAGCCCTCTCCCCCCCCCATCCCCTTCTGAGAGTGGTCAATGTTT T G GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100679605..100680004 32194978 MeRIP-seq:(Medium) rs1246246057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5122846,Human_RBP_ID_17092668,Human_RBP_ID_24180153,Human_RBP_ID_27527265 Human_miRNA_ID_1705769,Human_miRNA_ID_2384347 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74528 RMVar_ID_74528 Human_SNP_ID_332722359 m1A Human chr7 + 100680346 100680346 100680346 TGCCCTAATACTGCACTCTGAGCAATGAGGTCAATGGGAGGAGCTGGATGAGAAACCCAAAAGAC TGCCCTAATACTGCACTCTGAGCAATGAGGTCGATGGGAGGAGCTGGATGAGAAACCCAAAAGAC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100680295..100680362 26863196 MeRIP-seq:(Medium) rs922756056 Functional Loss SNV dbSNP153 33..33 33 - - - 74529 RMVar_ID_74529 Human_SNP_ID_332722979 m1A Human chr7 - 100681624 100681608 100681624 GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCACAGGAAGAGGCAGGGGCGGGGTCCCCAGCACTTG GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCAC________________GGGGTCCCCAGCACTTG CGCCCCTGCCTCTTCCT C GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100681573..100681691 26863196 MeRIP-seq:(Medium) rs1277028460 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_85000,Human_RBP_ID_15945504 Human_miRNA_ID_626419 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74530 RMVar_ID_74530 Human_SNP_ID_332722991 m1A Human chr7 - 100681624 100681624 100681624 GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCACAGGAAGAGGCAGGGGCGGGGTCCCCAGCACTTG GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCACGGGAAGAGGCAGGGGCGGGGTCCCCAGCACTTG T C GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100681573..100681691 26863196 MeRIP-seq:(Medium) rs1010739223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85000,Human_RBP_ID_15945504 Human_miRNA_ID_626419 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74531 RMVar_ID_74531 Human_SNP_ID_332722992 m1A Human chr7 - 100681624 100681624 100681624 GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCACAGGAAGAGGCAGGGGCGGGGTCCCCAGCACTTG GTCCCAGCCTGCAGGCTCCCCGCAGAGAGCACCGGAAGAGGCAGGGGCGGGGTCCCCAGCACTTG T G GIGYF1 Ensembl:ENSG00000146830 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100681573..100681691 26863196 MeRIP-seq:(Medium) rs1010739223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85000,Human_RBP_ID_15945504 Human_miRNA_ID_626419 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_93751,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247152,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74532 RMVar_ID_74532 Human_SNP_ID_332723437 m1A Human chr7 - 100682426 100682424 100682427 TCGGCCCATTCGCAAAAAGACGGAGGAAGAAGAGAAGCTGCTGAAGCTGCTGCAGGGCATTCCCA TCGGCCCATTCGCAAAAAGACGGAGGAAGAA___AAGCTGCTGAAGCTGCTGCAGGGCATTCCCA TCTC T GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100682376..100682500 26863196 MeRIP-seq:(Medium) rs1253577735 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_85004,Human_RBP_ID_15945518,Human_RBP_ID_18414211 Human_Splice_Rec_900228,Human_Splice_Rec_900282 Human_miRNA_ID_3117130 RMVar_hsa_circ_75749,RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_104198,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247151,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_315043,RMVar_hsa_circ_247154 74533 RMVar_ID_74533 Human_SNP_ID_332723603 m1A Human chr7 - 100682687 100682687 100682687 TGTGGGGCGGGCCAGACAAGAGTGGGGGCGGCAGCAGCGGCCTGGGGCTCTGGGAGGACACCCCC TGTGGGGCGGGCCAGACAAGAGTGGGGGCGGCGGCAGCGGCCTGGGGCTCTGGGAGGACACCCCC T C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100682638..100682757 26863196 MeRIP-seq:(Medium) rs750421292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85005,Human_RBP_ID_253542,Human_RBP_ID_793618,Human_RBP_ID_3971153,Human_RBP_ID_9311917,Human_RBP_ID_19019962,Human_RBP_ID_22623328,Human_RBP_ID_23116958 Human_Splice_Rec_900226,Human_Splice_Rec_900227,Human_Splice_Rec_900280,Human_Splice_Rec_900281 RMVar_hsa_circ_75749,RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_247154 74534 RMVar_ID_74534 Human_SNP_ID_332723604 m1A Human chr7 - 100682687 100682687 100682687 TGTGGGGCGGGCCAGACAAGAGTGGGGGCGGCAGCAGCGGCCTGGGGCTCTGGGAGGACACCCCC TGTGGGGCGGGCCAGACAAGAGTGGGGGCGGCCGCAGCGGCCTGGGGCTCTGGGAGGACACCCCC T G GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100682638..100682757 26863196 MeRIP-seq:(Medium) rs750421292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85005,Human_RBP_ID_253542,Human_RBP_ID_793618,Human_RBP_ID_3971153,Human_RBP_ID_9311917,Human_RBP_ID_19019962,Human_RBP_ID_22623328,Human_RBP_ID_23116958 Human_Splice_Rec_900226,Human_Splice_Rec_900227,Human_Splice_Rec_900280,Human_Splice_Rec_900281 RMVar_hsa_circ_75749,RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_114807,RMVar_hsa_circ_110960,RMVar_hsa_circ_95710,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247149,RMVar_hsa_circ_247150,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_247154 74535 RMVar_ID_74535 Human_SNP_ID_332723966 m1A Human chr7 - 100683350 100683348 100683351 AGAGGAGAAGCGCCGCCAGCAGCAGCAGGAGGAGCAGAAGCGGCGGCAGGAGGAGGAAGAGCTGT AGAGGAGAAGCGCCGCCAGCAGCAGCAGGAG___CAGAAGCGGCGGCAGGAGGAGGAAGAGCTGT GCTC G GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100683226..100683450 26863196 MeRIP-seq:(Medium) rs1243143060 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_85007,Human_RBP_ID_8237924,Human_RBP_ID_9403713,Human_RBP_ID_18472361,Human_RBP_ID_19019966,Human_RBP_ID_21993916,Human_RBP_ID_23080115,Human_RBP_ID_26356837,Human_RBP_ID_27829619 Human_Splice_Rec_900222,Human_Splice_Rec_900223,Human_Splice_Rec_900276,Human_Splice_Rec_900277 RMVar_hsa_circ_75749,RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_9957,RMVar_hsa_circ_247154,RMVar_hsa_circ_86149,RMVar_hsa_circ_247156,RMVar_hsa_circ_247157 74536 RMVar_ID_74536 Human_SNP_ID_332724408 m1A Human chr7 - 100684097 100684088 100684097 GAAAAGGCAGCTCTGGGGGACCTGACACCGCCACCACCGCCGCCGCCACAGCAGCAGCAGCAGCA GAAAAGGCAGCTCTGGGGGACCTGACACCGCC_________GCCGCCACAGCAGCAGCAGCAGCA CGGCGGTGGT C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100684051..100684187;chr7:100684051..100684259 26863196 MeRIP-seq:(Medium) rs748295028 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_8652614 Human_Splice_Rec_900216,Human_Splice_Rec_900217,Human_Splice_Rec_900270,Human_Splice_Rec_900271,Human_Splice_Rec_900291 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74537 RMVar_ID_74537 Human_SNP_ID_332724421 m1A Human chr7 - 100684097 100684097 100684097 GAAAAGGCAGCTCTGGGGGACCTGACACCGCCACCACCGCCGCCGCCACAGCAGCAGCAGCAGCA GAAAAGGCAGCTCTGGGGGACCTGACACCGCCGCCACCGCCGCCGCCACAGCAGCAGCAGCAGCA T C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100684051..100684187;chr7:100684051..100684259 26863196 MeRIP-seq:(Medium) rs371552448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8652614 Human_Splice_Rec_900216,Human_Splice_Rec_900217,Human_Splice_Rec_900270,Human_Splice_Rec_900271,Human_Splice_Rec_900291 RMVar_hsa_circ_79512,RMVar_hsa_circ_110834,RMVar_hsa_circ_113134,RMVar_hsa_circ_123158,RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247147,RMVar_hsa_circ_247148,RMVar_hsa_circ_247145,RMVar_hsa_circ_247146,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140 74538 RMVar_ID_74538 Human_SNP_ID_332725494 m1A Human chr7 - 100686318 100686318 100686318 GGGTGTGGTGAAGAGGAGGGGCGGGGAGGGGGAGGCAGCTCTCACCTGCGGCGGTGCCGAGCGCC GGGTGTGGTGAAGAGGAGGGGCGGGGAGGGGGGGGCAGCTCTCACCTGCGGCGGTGCCGAGCGCC T C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100686149..100688310;chr7:100685326..100687425 26863196 MeRIP-seq:(Medium) rs1402661203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85014,Human_RBP_ID_253549,Human_RBP_ID_793621,Human_RBP_ID_844431,Human_RBP_ID_954747,Human_RBP_ID_3971165,Human_RBP_ID_5403283,Human_RBP_ID_8238301,Human_RBP_ID_8944181,Human_RBP_ID_9438959,Human_RBP_ID_19019979,Human_RBP_ID_22111044,Human_RBP_ID_22483045,Human_RBP_ID_22554872,Human_RBP_ID_22687156,Human_RBP_ID_22747112,Human_RBP_ID_23080378,Human_RBP_ID_23116903,Human_RBP_ID_24549217,Human_RBP_ID_24554962,Human_RBP_ID_26051409,Human_RBP_ID_26356844,Human_RBP_ID_26772081,Human_RBP_ID_27829621 Human_miRNA_ID_2241034 RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_50574 74539 RMVar_ID_74539 Human_SNP_ID_332725530 m1A Human chr7 - 100686382 100686382 100686382 TGGCTGGCGGGAACATGGGGAACGGCGGCGCAAGTTTGAATTTGATTTGCGAGGGGATCGAGGAG TGGCTGGCGGGAACATGGGGAACGGCGGCGCAGGTTTGAATTTGATTTGCGAGGGGATCGAGGAG T C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100686226..100686464 26863196 MeRIP-seq:(Medium) rs910324775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5622383,Human_RBP_ID_8652615 Human_Splice_Rec_900202,Human_Splice_Rec_900256,Human_Splice_Rec_900302 RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_50574 74540 RMVar_ID_74540 Human_SNP_ID_332725531 m1A Human chr7 - 100686382 100686382 100686382 TGGCTGGCGGGAACATGGGGAACGGCGGCGCAAGTTTGAATTTGATTTGCGAGGGGATCGAGGAG TGGCTGGCGGGAACATGGGGAACGGCGGCGCACGTTTGAATTTGATTTGCGAGGGGATCGAGGAG T G GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100686226..100686464 26863196 MeRIP-seq:(Medium) rs910324775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5622383,Human_RBP_ID_8652615 Human_Splice_Rec_900202,Human_Splice_Rec_900256,Human_Splice_Rec_900302 RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_50574 74541 RMVar_ID_74541 Human_SNP_ID_332726672 m1A Human chr7 + 100688610 100688608 100688611 GGCCCGGGGCTCACCTGGCAGCCTGGCCCGGGAAGAAGGAGGGCAGGGGCTGGTGCTGGAGTGAA GGCCCGGGGCTCACCTGGCAGCCTGGCCCGG___GAAGGAGGGCAGGGGCTGGTGCTGGAGTGAA GGAA G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100687595..100688901 32194978 MeRIP-seq:(Medium) rs746097448 Functional Loss DEL dbSNP153 32..34 33 - - - 74542 RMVar_ID_74542 Human_SNP_ID_332727603 m1A Human chr7 + 100691660 100691660 100691660 GCCCGTCTCAGCTTACCCGGCTGAGCTTTCTCAGCTCAGGGTCTCCTTCTCACAGGCCCCTTCCA GCCCGTCTCAGCTTACCCGGCTGAGCTTTCTCCGCTCAGGGTCTCCTTCTCACAGGCCCCTTCCA A C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100691658..100691766 26863196 MeRIP-seq:(Medium) rs1172705657 Functional Loss SNV dbSNP153 33..33 33 - - - 74543 RMVar_ID_74543 Human_SNP_ID_332728382 m1A Human chr7 - 100694013 100694013 100694013 ACGCCGCGGCGGCCGCGCCGAGCCCGCGAGCTAGAGAAGCGCCGGAGCCAGCGCGCGGGCCGCCA ACGCCGCGGCGGCCGCGCCGAGCCCGCGAGCTGGAGAAGCGCCGGAGCCAGCGCGCGGGCCGCCA T C GIGYF1 Ensembl:ENSG00000146830 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100694001..100694225 26863410 MeRIP-seq:(Medium) rs191319537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_900235,Human_Splice_Rec_900305 GWAS_ID_8929 74544 RMVar_ID_74544 Human_SNP_ID_332728454 m1A Human chr7 + 100694178 100694171 100694178 CGGCGCGCGGCGGGCGGGGGCCGGGGACGGCGACGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC CGGCGCGCGGCGGGCGGGGGCCGGGG_______CGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC GACGGCGA G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:100694026..100694250 26863410 MeRIP-seq:(Medium) rs1562890713 Functional Loss DEL dbSNP153 27..33 33 - - - 74545 RMVar_ID_74545 Human_SNP_ID_332728458 m1A Human chr7 + 100694178 100694178 100694178 CGGCGCGCGGCGGGCGGGGGCCGGGGACGGCGACGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC CGGCGCGCGGCGGGCGGGGGCCGGGGACGGCGGCGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:100694026..100694250 26863410 MeRIP-seq:(Medium) rs1222167506 Functional Loss SNV dbSNP153 33..33 33 - - - 74546 RMVar_ID_74546 Human_SNP_ID_332728459 m1A Human chr7 + 100694178 100694178 100694178 CGGCGCGCGGCGGGCGGGGGCCGGGGACGGCGACGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC CGGCGCGCGGCGGGCGGGGGCCGGGGACGGCGTCGGCGGCTAGCAGCGGGGGAGGGGGCGCTGGC A T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:100694026..100694250 26863410 MeRIP-seq:(Medium) rs1222167506 Functional Loss SNV dbSNP153 33..33 33 - - - 74547 RMVar_ID_74547 Human_SNP_ID_332728535 m1A Human chr7 + 100694312 100694309 100694312 CGCGGACGCGGGGCCGCGGGGCCGCCCCTTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCGGACGCGGGGCCGCGGGGCCGCCCCTT___CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC TCCA T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:100693976..100694386 26863196 MeRIP-seq:(Medium) rs1417993398 Functional Loss DEL dbSNP153 31..33 33 - - - 74548 RMVar_ID_74548 Human_SNP_ID_332728561 m1A Human chr7 + 100694312 100694312 100694312 CGCGGACGCGGGGCCGCGGGGCCGCCCCTTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCGGACGCGGGGCCGCGGGGCCGCCCCTTCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:100693976..100694386 26863196 MeRIP-seq:(Medium) rs1442018372 Functional Loss SNV dbSNP153 33..33 33 - - - 74549 RMVar_ID_74549 Human_SNP_ID_332728562 m1A Human chr7 + 100694312 100694312 100694312 CGCGGACGCGGGGCCGCGGGGCCGCCCCTTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCGGACGCGGGGCCGCGGGGCCGCCCCTTCCTCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC A T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:100693976..100694386 26863196 MeRIP-seq:(Medium) rs1442018372 Functional Loss SNV dbSNP153 33..33 33 - - - 74550 RMVar_ID_74550 Human_SNP_ID_332728664 m1A Human chr7 - 100694388 100694379 100694388 ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGGAGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGG_________GCGGCGGCGGCGGCGGCGGCGGCG CCGCCTCCCT C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:100694305..100694387 26863410 MeRIP-seq:(Medium) rs1354324226 Functional Loss DEL dbSNP153 33..41 33 - - - 74551 RMVar_ID_74551 Human_SNP_ID_332728674 m1A Human chr7 - 100694388 100694385 100694388 ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGGAGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGG___GAGGCGGCGGCGGCGGCGGCGGCGGCGGCG CCCT C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:100694305..100694387 26863410 MeRIP-seq:(Medium) rs1458120025 Functional Loss DEL dbSNP153 33..35 33 - - - 74552 RMVar_ID_74552 Human_SNP_ID_332728677 m1A Human chr7 - 100694388 100694388 100694388 ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGGAGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG ACGAGGAGAGGTGGCGCGGGCCGGAGCCGCGGCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG T G RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:100694305..100694387 26863410 MeRIP-seq:(Medium) rs1464332763 Functional Loss SNV dbSNP153 33..33 33 - - - 74553 RMVar_ID_74553 Human_SNP_ID_332731933 m1A Human chr7 - 100706173 100706173 100706173 CCAGAGAAAGAAGGATGTGGGTGCAAGCAGCCAGCCAGCTCGTGGGCGCCCTGCCCGCGCCGGGG CCAGAGAAAGAAGGATGTGGGTGCAAGCAGCCGGCCAGCTCGTGGGCGCCCTGCCCGCGCCGGGG T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100706126..100706325 26863196 MeRIP-seq:(Medium) rs182037615 Functional Loss SNV dbSNP153 33..33 33 - - - 74554 RMVar_ID_74554 Human_SNP_ID_332731934 m1A Human chr7 - 100706173 100706173 100706173 CCAGAGAAAGAAGGATGTGGGTGCAAGCAGCCAGCCAGCTCGTGGGCGCCCTGCCCGCGCCGGGG CCAGAGAAAGAAGGATGTGGGTGCAAGCAGCCCGCCAGCTCGTGGGCGCCCTGCCCGCGCCGGGG T G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100706126..100706325 26863196 MeRIP-seq:(Medium) rs182037615 Functional Loss SNV dbSNP153 33..33 33 - - - 74555 RMVar_ID_74555 Human_SNP_ID_332732114 m1A Human chr7 - 100706785 100706785 100706785 GCGTGGGAAAGGGACGCGATCAGAGGGCTCAGAGGGACCTCGAAGCCTTTCCTACCCCTTTTCCT GCGTGGGAAAGGGACGCGATCAGAGGGCTCAGGGGGACCTCGAAGCCTTTCCTACCCCTTTTCCT T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100706782..100706931 26863196 MeRIP-seq:(Medium) rs547567238 Functional Loss SNV dbSNP153 33..33 33 - - - 74556 RMVar_ID_74556 Human_SNP_ID_332763385 m1A Human chr7 - 100813203 100813203 100813203 CTGACGGGGCCCTGCCTGATTTCTCAGGTACTAAGGTCTACATCGACCCCTTCACTTATGAAGAC CTGACGGGGCCCTGCCTGATTTCTCAGGTACTGAGGTCTACATCGACCCCTTCACTTATGAAGAC T C EPHB4 Ensembl:ENSG00000196411 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100813069..100813217 26863196 MeRIP-seq:(Medium) rs1484495683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_901072,Human_Splice_Rec_901096,Human_Splice_Rec_901128,Human_Splice_Rec_901158,Human_Splice_Rec_901176 RMVar_hsa_circ_19752,RMVar_hsa_circ_13997,RMVar_hsa_circ_80807,RMVar_hsa_circ_88378,RMVar_hsa_circ_101224,RMVar_hsa_circ_247162,RMVar_hsa_circ_247163,RMVar_hsa_circ_60863,RMVar_hsa_circ_247164,RMVar_hsa_circ_48921,RMVar_hsa_circ_275314,RMVar_hsa_circ_247165,RMVar_hsa_circ_82594,RMVar_hsa_circ_336030,RMVar_hsa_circ_369973,RMVar_hsa_circ_98542,RMVar_hsa_circ_88198,RMVar_hsa_circ_247167,RMVar_hsa_circ_247169,RMVar_hsa_circ_247170,RMVar_hsa_circ_247171,RMVar_hsa_circ_247168,RMVar_hsa_circ_125694,RMVar_hsa_circ_375035,RMVar_hsa_circ_102547,RMVar_hsa_circ_247172,RMVar_hsa_circ_247173,RMVar_hsa_circ_247174 74557 RMVar_ID_74557 Human_SNP_ID_332765619 m1A Human chr7 + 100819881 100819857 100819882 GTTCAGGCGGGAAACCACGCTCCGCGGAGCCGAAGGAGGGGCTGCAGGAGACCAGGGAGTCAGGC GTTCAGGCG_________________________GGAGGGGCTGCAGGAGACCAGGGAGTCAGGC GGGAAACCACGCTCCGCGGAGCCGAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100819661..100819912 26863196 MeRIP-seq:(Medium) rs1174960880 Functional Loss DEL dbSNP153 10..34 33 - - - 74558 RMVar_ID_74558 Human_SNP_ID_332766415 m1A Human chr7 - 100822227 100822227 100822227 AGCTTCCCCTGCGACTGCTGCTCATCCGGGGGAGAGTCCTGAACTCCACTCAGGACCCACTTCTT AGCTTCCCCTGCGACTGCTGCTCATCCGGGGGGGAGTCCTGAACTCCACTCAGGACCCACTTCTT T C EPHB4 Ensembl:ENSG00000196411 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100822225..100822326 26863196 MeRIP-seq:(Medium) rs1195345281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19135311,Human_RBP_ID_24180205 RMVar_hsa_circ_13997,RMVar_hsa_circ_98542,RMVar_hsa_circ_247171,RMVar_hsa_circ_125694,RMVar_hsa_circ_48608,RMVar_hsa_circ_247174,RMVar_hsa_circ_98489,RMVar_hsa_circ_247175 74559 RMVar_ID_74559 Human_SNP_ID_332767088 m1A Human chr7 - 100823927 100823927 100823927 CCCCTTGCTGACCTCCTTCTCTGCACAGTGGGAGGAACTGAGCGGCCTGGATGAGGAACAGCACA CCCCTTGCTGACCTCCTTCTCTGCACAGTGGGTGGAACTGAGCGGCCTGGATGAGGAACAGCACA T A EPHB4 Ensembl:ENSG00000196411 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100823801..100823984 26863196 MeRIP-seq:(Medium) rs773705502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14496,Human_RBP_ID_792617,Human_RBP_ID_843957,Human_RBP_ID_952670,Human_RBP_ID_3972300,Human_RBP_ID_4917876,Human_RBP_ID_5090513,Human_RBP_ID_9403726,Human_RBP_ID_18472443,Human_RBP_ID_19019996,Human_RBP_ID_22685708 Human_Splice_Rec_901056,Human_Splice_Rec_901086,Human_Splice_Rec_901112,Human_Splice_Rec_901142,Human_Splice_Rec_901190,Human_Splice_Rec_901206 RMVar_hsa_circ_98542,RMVar_hsa_circ_247171,RMVar_hsa_circ_125694,RMVar_hsa_circ_247174 74560 RMVar_ID_74560 Human_SNP_ID_332768309 m1A Human chr7 - 100827314 100827296 100827315 GCTCAGCCCCCGCCACCCGGGGCGGGACCCCGAGGCCCCGGAGGGACCCCAACTCCAGCCACGTC GCTCAGCCCCCGCCACCCGGGGCGGGACCCC___________________AACTCCAGCCACGTC TGGGGTCCCTCCGGGGCCTC T EPHB4 Ensembl:ENSG00000196411 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100827268..100827495 26863196 MeRIP-seq:(Medium) rs1314374023 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_794707,Human_RBP_ID_4955927,Human_RBP_ID_9337294,Human_RBP_ID_18196023,Human_RBP_ID_22463681,Human_RBP_ID_22534338 74561 RMVar_ID_74561 Human_SNP_ID_332768371 m1A Human chr7 + 100827461 100827461 100827461 GTGGGAGCCCGAGCGGGGACGGAGCGGGAGGGAGGGAGACTGCGGCGCGGAGCCGGGCGGGCCGG GTGGGAGCCCGAGCGGGGACGGAGCGGGAGGGTGGGAGACTGCGGCGCGGAGCCGGGCGGGCCGG A T SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr7:100827370..100827521 26863410 MeRIP-seq:(Medium) rs1380785540 Functional Loss SNV dbSNP153 33..33 33 - - - 74562 RMVar_ID_74562 Human_SNP_ID_332768378 m1A Human chr7 + 100827479 100827479 100827479 ACGGAGCGGGAGGGAGGGAGACTGCGGCGCGGAGCCGGGCGGGCCGGGCCGGGCAGGGGCTGAGC ACGGAGCGGGAGGGAGGGAGACTGCGGCGCGGGGCCGGGCGGGCCGGGCCGGGCAGGGGCTGAGC A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100827301..100827543 26863410 MeRIP-seq:(Medium) rs1429786106 Functional Loss SNV dbSNP153 33..33 33 - - - 74563 RMVar_ID_74563 Human_SNP_ID_332770813 m1A Human chr7 + 100836219 100836219 100836219 GGCTGGCTCTAGGAGGGAAAGTAAGAAGGACTATTTGTGGCTGGAGGCCAGGATACCGGGGTCTG GGCTGGCTCTAGGAGGGAAAGTAAGAAGGACTGTTTGTGGCTGGAGGCCAGGATACCGGGGTCTG A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100836217..100836372 26863196 MeRIP-seq:(Medium) rs975538806 Functional Loss SNV dbSNP153 33..33 33 - - - 74564 RMVar_ID_74564 Human_SNP_ID_332772073 m1A Human chr7 + 100840583 100840583 100840583 AGAGGCAAAGAAAGACCAGCAGAAAGAGAGAAAGGAAAGAGACAGAGAGGAAGAGACAGAGAGGA AGAGGCAAAGAAAGACCAGCAGAAAGAGAGAAGGGAAAGAGACAGAGAGGAAGAGACAGAGAGGA A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100840581..100840721 26863196 MeRIP-seq:(Medium) rs1368239177 Functional Loss SNV dbSNP153 33..33 33 - - - 74565 RMVar_ID_74565 Human_SNP_ID_332775736 m1A Human chr7 + 100854312 100854309 100854313 GTCCTGGAGGGGCGTCTGCCCGGAAGCTGTCCACCTTCCTGGGTGTGGTGGTGCCCACTGTCCTG GTCCTGGAGGGGCGTCTGCCCGGAAGCTGT____CTTCCTGGGTGTGGTGGTGCCCACTGTCCTG TCCAC T SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:100854228..100854354 26863196 MeRIP-seq:(Medium) rs1344994574 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4955929,Human_RBP_ID_21398426 Human_Splice_Rec_901219,Human_Splice_Rec_901245,Human_Splice_Rec_901291,Human_Splice_Rec_901313,Human_Splice_Rec_901319,Human_Splice_Rec_901331 RMVar_hsa_circ_247180 74566 RMVar_ID_74566 Human_SNP_ID_332776466 m1A Human chr7 - 100856970 100856970 100856970 GGAATGAGGCCCGGGCATAGAGGCCGGCTCCCAGGGTGCAGACCCCACCCACAAGGCCCAGCAGC GGAATGAGGCCCGGGCATAGAGGCCGGCTCCCGGGGTGCAGACCCCACCCACAAGGCCCAGCAGC T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100856920..100857071 32194978 MeRIP-seq:(Medium) rs1386835980 Functional Loss SNV dbSNP153 33..33 33 - - - 74567 RMVar_ID_74567 Human_SNP_ID_332776914 m1A Human chr7 - 100858631 100858631 100858631 CGTCCCCCCAGTGCTCCGATATTCCTCCCTCCAGACCCTAATCCACGCTCTTTTATTTATTTATT CGTCCCCCCAGTGCTCCGATATTCCTCCCTCCGGACCCTAATCCACGCTCTTTTATTTATTTATT T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100858623..100858744 26863196 MeRIP-seq:(Medium) rs1415883239 Functional Loss SNV dbSNP153 33..33 33 - - - 74568 RMVar_ID_74568 Human_SNP_ID_332779290 m1A Human chr7 + 100866316 100866316 100866316 GGCTGGGGAACCCGAGGCGGAGGAGGAAGGGGACTTTGTGAACAGTGGGCGGGGAGACGCAGAGG GGCTGGGGAACCCGAGGCGGAGGAGGAAGGGGTCTTTGTGAACAGTGGGCGGGGAGACGCAGAGG A T SLC12A9 Ensembl:ENSG00000146828 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100866138..100866552 26863196 MeRIP-seq:(Medium) rs1348800956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19020001,Human_RBP_ID_22775034 RMVar_hsa_circ_104930,RMVar_hsa_circ_86458,RMVar_hsa_circ_127437,RMVar_hsa_circ_247186,RMVar_hsa_circ_247187,RMVar_hsa_circ_96823,RMVar_hsa_circ_247188,RMVar_hsa_circ_247189 74569 RMVar_ID_74569 Human_SNP_ID_332779389 m1A Human chr7 - 100866526 100866526 100866526 TGGGGCCCAGGTCTCGGGTTAGAGTCTCCAGTAGCGCCAGGTAGCGGGGGTATCGGGCGGGATCG TGGGGCCCAGGTCTCGGGTTAGAGTCTCCAGTGGCGCCAGGTAGCGGGGGTATCGGGCGGGATCG T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:100866449..100866534 26863410 MeRIP-seq:(Medium) rs1457217371 Functional Loss SNV dbSNP153 33..33 33 - - - 74570 RMVar_ID_74570 Human_SNP_ID_332779748 m1A Human chr7 + 100867576 100867566 100867576 GAGCCCCTCAGGGGAGGGCGATCCCCCGCGGCACCCCGGGGCCACCACCGGCCCACGGAGCAGGT GAGCCCCTCAGGGGAGGGCGATC__________CCCCGGGGCCACCACCGGCCCACGGAGCAGGT CCCCCGCGGCA C TRIP6 Ensembl:ENSG00000087077 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:100867526..100867575 26863196 MeRIP-seq:(Medium) rs941897896 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_254123,Human_RBP_ID_4956556 Human_Splice_Rec_901397,Human_Splice_Rec_901399,Human_Splice_Rec_901409,Human_Splice_Rec_901425,Human_Splice_Rec_901439,Human_Splice_Rec_901447 74571 RMVar_ID_74571 Human_SNP_ID_332779889 m1A Human chr7 + 100867925 100867925 100867925 CCCCTTCCATCTGAGCAGTGTTACCAGGCCCCAGGGGGACCGGAGGATCGGGGGCCGGCGTGGGT CCCCTTCCATCTGAGCAGTGTTACCAGGCCCCGGGGGGACCGGAGGATCGGGGGCCGGCGTGGGT A G TRIP6 Ensembl:ENSG00000087077 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100867876..100867925 26863196 MeRIP-seq:(Medium) rs900766200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792868,Human_RBP_ID_23215871 Human_Splice_Rec_901398,Human_Splice_Rec_901400,Human_Splice_Rec_901401,Human_Splice_Rec_901410,Human_Splice_Rec_901411,Human_Splice_Rec_901426,Human_Splice_Rec_901427 Human_miRNA_ID_2436430 RMVar_hsa_circ_5875,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190 74572 RMVar_ID_74572 Human_SNP_ID_332779910 m1A Human chr7 - 100867967 100867967 100867967 CCGGGTCTCACCTGCGTGTGCTGGAGTACTCCATGGGACCCCACCCACGCCGGCCCCCGATCCTC CCGGGTCTCACCTGCGTGTGCTGGAGTACTCCGTGGGACCCCACCCACGCCGGCCCCCGATCCTC T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr7:100867834..100868021;chr7:100867901..100868150 26863196 MeRIP-seq:(Medium) rs760153746 Functional Loss SNV dbSNP153 33..33 33 - - - 74573 RMVar_ID_74573 Human_SNP_ID_332780032 m1A Human chr7 + 100868224 100868224 100868224 AATGGGGGTCGGGGTCATGCGTCACGGCGACCAGACCGACAGGTGACTCTGCCCCTCCTCCCCGT AATGGGGGTCGGGGTCATGCGTCACGGCGACCGGACCGACAGGTGACTCTGCCCCTCCTCCCCGT A G TRIP6 Ensembl:ENSG00000087077 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:100868176..100868250 26863196 MeRIP-seq:(Medium) rs769279607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_901403,Human_Splice_Rec_901413,Human_Splice_Rec_901429,Human_Splice_Rec_901441,Human_Splice_Rec_901449 RMVar_hsa_circ_5875,RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_247191 74574 RMVar_ID_74574 Human_SNP_ID_332780202 m1A Human chr7 + 100868643 100868640 100868644 CAGCACCCCGGCTGGCCCAGCCTTCCCCGTGCAAGTGAAGGTGGCACAGCCAGTGAGGGGCTGCG CAGCACCCCGGCTGGCCCAGCCTTCCCCGT____GTGAAGGTGGCACAGCCAGTGAGGGGCTGCG TGCAA T TRIP6 Ensembl:ENSG00000087077 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100868501..100868700 26863196 MeRIP-seq:(Medium) rs1347039381 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4958456 Human_miRNA_ID_338511 RMVar_hsa_circ_5875,RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_247191,RMVar_hsa_circ_332446 74575 RMVar_ID_74575 Human_SNP_ID_332780276 m1A Human chr7 + 100868801 100868801 100868801 ATAGGAGCCAGAGAGAGCCAGGGCCAGGGGCCAAAGAGGAAGCTGCTGGGGTCTCTGGCCCTGCA ATAGGAGCCAGAGAGAGCCAGGGCCAGGGGCCCAAGAGGAAGCTGCTGGGGTCTCTGGCCCTGCA A C TRIP6 Ensembl:ENSG00000087077 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100868776..100868800 26863196 MeRIP-seq:(Medium) rs1480779070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_901405,Human_Splice_Rec_901415,Human_Splice_Rec_901431,Human_Splice_Rec_901443,Human_Splice_Rec_901451,Human_Splice_Rec_901461,Human_Splice_Rec_901465 RMVar_hsa_circ_5875,RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_332446,RMVar_hsa_circ_247192 74576 RMVar_ID_74576 Human_SNP_ID_332780285 m1A Human chr7 - 100868824 100868824 100868824 TGCTCGCCTCCTCTTCCTCTTCCTGCAGGGCCAGAGACCCCAGCAGCTTCCTCTTTGGCCCCTGG TGCTCGCCTCCTCTTCCTCTTCCTGCAGGGCCGGAGACCCCAGCAGCTTCCTCTTTGGCCCCTGG T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100868514..100868907 26863196 MeRIP-seq:(Medium) rs770100190 Functional Loss SNV dbSNP153 33..33 33 - - - 74577 RMVar_ID_74577 Human_SNP_ID_332780298 m1A Human chr7 + 100868843 100868843 100868843 CTGCTGGGGTCTCTGGCCCTGCAGGAAGAGGAAGAGGAGGCGAGCACGGGCCCCAGGTGAGCCCT CTGCTGGGGTCTCTGGCCCTGCAGGAAGAGGAGGAGGAGGCGAGCACGGGCCCCAGGTGAGCCCT A G TRIP6 Ensembl:ENSG00000087077 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100868826..100868850 26863196 MeRIP-seq:(Medium) rs1282429749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5153015,Human_RBP_ID_22464647,Human_RBP_ID_26358067 Human_Splice_Rec_901405,Human_Splice_Rec_901415,Human_Splice_Rec_901431,Human_Splice_Rec_901443,Human_Splice_Rec_901451,Human_Splice_Rec_901461,Human_Splice_Rec_901465 Human_miRNA_ID_731498 RMVar_hsa_circ_5875,RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_332446,RMVar_hsa_circ_247192 74578 RMVar_ID_74578 Human_SNP_ID_332780744 m1A Human chr7 + 100870339 100870339 100870339 GAGGGCCCTGGTATTACAGCATCAGGAGCTAGAGTAGGACCGAGCCCGATTCCCACCTTCCAGGT GAGGGCCCTGGTATTACAGCATCAGGAGCTAGCGTAGGACCGAGCCCGATTCCCACCTTCCAGGT A C TRIP6 Ensembl:ENSG00000087077 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100870337..100870912 26863196 MeRIP-seq:(Medium) rs1452908954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15945966 RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_247192 74579 RMVar_ID_74579 Human_SNP_ID_332780816 m1A Human chr7 - 100870462 100870462 100870462 ACGTCCCACCCACCCCACAGCCTCAGCTCACCAAAGTACTCCCCGCTGGGCGGGTGGTTCATGTC ACGTCCCACCCACCCCACAGCCTCAGCTCACCGAAGTACTCCCCGCTGGGCGGGTGGTTCATGTC T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:100870351..100870931;chr7:100870351..100870475 26863196 MeRIP-seq:(Medium) rs146388109 Functional Loss SNV dbSNP153 33..33 33 - - - 74580 RMVar_ID_74580 Human_SNP_ID_332781240 m1A Human chr7 - 100871673 100871673 100871673 TGCAGTGGATCTGGCTCGTAGCATCCACTGTGAAGGGGATGCCGTCGAGGCCGCGGTGACACACC TGCAGTGGATCTGGCTCGTAGCATCCACTGTGGAGGGGATGCCGTCGAGGCCGCGGTGACACACC T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100871160..100872625 32194978 MeRIP-seq:(Medium) rs756107564 Functional Loss SNV dbSNP153 33..33 33 - - - 74581 RMVar_ID_74581 Human_SNP_ID_332781599 m1A Human chr7 - 100872730 100872730 100872730 GTGCTGGGGGCCCCTGACCTCGCACTTGTAACAGCCAATGTGAAAACTTCGATCCAGAGCAACAA GTGCTGGGGGCCCCTGACCTCGCACTTGTAACGGCCAATGTGAAAACTTCGATCCAGAGCAACAA T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100872680..100872795 26863196 MeRIP-seq:(Medium) rs771447927 Functional Loss SNV dbSNP153 33..33 33 - - - 74582 RMVar_ID_74582 Human_SNP_ID_332781776 m1A Human chr7 + 100873245 100873245 100873245 CTGCTACCCGCTGGATGGGCACATCTTGTGCAAGGCCTGCAGCGCCTGGCGCATCCAGGAGCTCT CTGCTACCCGCTGGATGGGCACATCTTGTGCAGGGCCTGCAGCGCCTGGCGCATCCAGGAGCTCT A G TRIP6 Ensembl:ENSG00000087077 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100872771..100873425 32194978 MeRIP-seq:(Medium) rs1354745951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15946041,Human_RBP_ID_17427395,Human_RBP_ID_22111052 Human_Splice_Rec_901424,Human_Splice_Rec_901438,Human_Splice_Rec_901460 Human_miRNA_ID_1965757,Human_miRNA_ID_2361213 RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_126846,RMVar_hsa_circ_247192,RMVar_hsa_circ_95429,RMVar_hsa_circ_247193,RMVar_hsa_circ_247194 74583 RMVar_ID_74583 Human_SNP_ID_332781811 m1A Human chr7 + 100873318 100873318 100873318 GTCACCACTGACTGCTGAGTCTTCCTAGAAGTACCTGCTGGGTTCTCAGTTCCAGTTCCCATCCT GTCACCACTGACTGCTGAGTCTTCCTAGAAGTCCCTGCTGGGTTCTCAGTTCCAGTTCCCATCCT A C TRIP6 Ensembl:ENSG00000087077 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100873269..100873450 26863196 MeRIP-seq:(Medium) rs781066528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671574,Human_RBP_ID_1049505,Human_RBP_ID_1679461,Human_RBP_ID_15946048,Human_RBP_ID_21398474 Human_miRNA_ID_2221109,Human_miRNA_ID_2484156,Human_miRNA_ID_2927733,Human_miRNA_ID_3072533 RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_126846,RMVar_hsa_circ_247192,RMVar_hsa_circ_95429,RMVar_hsa_circ_247193,RMVar_hsa_circ_247194 74584 RMVar_ID_74584 Human_SNP_ID_332782396 m1A Human chr7 - 100875200 100875200 100875200 AGACGGAGACGGAGCTCTTGAGTAGAGGGCCGAAGAGAGGCGAACAAAAGTGGGACAACCGGGGA AGACGGAGACGGAGCTCTTGAGTAGAGGGCCGCAGAGAGGCGAACAAAAGTGGGACAACCGGGGA T G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100875151..100875300 26863196 MeRIP-seq:(Medium) rs1300927636 Functional Loss SNV dbSNP153 33..33 33 - - - 74585 RMVar_ID_74585 Human_SNP_ID_332782409 m1A Human chr7 - 100875220 100875220 100875220 CGAGGACTTCGAGGAGGGCGAGACGGAGACGGAGCTCTTGAGTAGAGGGCCGAAGAGAGGCGAAC CGAGGACTTCGAGGAGGGCGAGACGGAGACGGCGCTCTTGAGTAGAGGGCCGAAGAGAGGCGAAC T G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100875126..100875368;chr7:100875126..100875300 26863196 MeRIP-seq:(Medium) rs1451497751 Functional Loss SNV dbSNP153 33..33 33 - - - 74586 RMVar_ID_74586 Human_SNP_ID_332784763 m1A Human chr7 + 100882145 100882145 100882145 GGAGTTTCTCCTCTCCCTGGATGACTCGGTGGATGAGACGGAGGCCGTCAAGCGCTATAATGACT GGAGTTTCTCCTCTCCCTGGATGACTCGGTGGGTGAGACGGAGGCCGTCAAGCGCTATAATGACT A G SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100881314..100882200 32194978 MeRIP-seq:(Medium) rs200061976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842791,Human_RBP_ID_2031731,Human_RBP_ID_4918072,Human_RBP_ID_5428939,Human_RBP_ID_8906488,Human_RBP_ID_9403730,Human_RBP_ID_15946221,Human_RBP_ID_19021319,Human_RBP_ID_24389127,Human_RBP_ID_24548980,Human_RBP_ID_26356049,Human_RBP_ID_27830600 Human_Splice_Rec_901484,Human_Splice_Rec_901485,Human_Splice_Rec_901522,Human_Splice_Rec_901523,Human_Splice_Rec_901560,Human_Splice_Rec_901561,Human_Splice_Rec_901604,Human_Splice_Rec_901605,Human_Splice_Rec_901642,Human_Splice_Rec_901643,Human_Splice_Rec_901647 RMVar_hsa_circ_103373,RMVar_hsa_circ_111923,RMVar_hsa_circ_247196,RMVar_hsa_circ_247197,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326 74587 RMVar_ID_74587 Human_SNP_ID_332785417 m1A Human chr7 + 100884234 100884234 100884234 AGACAAAGCTGATGCCATTGTCAAGATGCTGGATGCAGGTGTGCGGATTTGGAGGGGTGGCAGGC AGACAAAGCTGATGCCATTGTCAAGATGCTGGGTGCAGGTGTGCGGATTTGGAGGGGTGGCAGGC A G SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100884067..100884250 26863196 MeRIP-seq:(Medium) rs763587033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1679498,Human_RBP_ID_2031739,Human_RBP_ID_8906496,Human_RBP_ID_9403733,Human_RBP_ID_19020007,Human_RBP_ID_22514907 Human_Splice_Rec_901487,Human_Splice_Rec_901525,Human_Splice_Rec_901563,Human_Splice_Rec_901607,Human_Splice_Rec_901653 RMVar_hsa_circ_103373,RMVar_hsa_circ_111923,RMVar_hsa_circ_247196,RMVar_hsa_circ_247197,RMVar_hsa_circ_95915,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326,RMVar_hsa_circ_268813,RMVar_hsa_circ_247200,RMVar_hsa_circ_247201 74588 RMVar_ID_74588 Human_SNP_ID_332785531 m1A Human chr7 + 100884473 100884473 100884473 AGGAAAGCCTGGGGAGCCCAGCAAGAAAGAAGAAGGACGGGCTGGAGCAGGCCTAGGGGACGGGG AGGAAAGCCTGGGGAGCCCAGCAAGAAAGAAGGAGGACGGGCTGGAGCAGGCCTAGGGGACGGGG A G SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100884451..100884475 32194978 MeRIP-seq:(Medium) rs370063149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14499,Human_RBP_ID_4918095,Human_RBP_ID_5628221,Human_RBP_ID_7666669,Human_RBP_ID_23080683,Human_RBP_ID_24180262,Human_RBP_ID_24548982,Human_RBP_ID_26051790,Human_RBP_ID_26356857 Human_Splice_Rec_901489,Human_Splice_Rec_901527,Human_Splice_Rec_901565,Human_Splice_Rec_901609 RMVar_hsa_circ_111923,RMVar_hsa_circ_247197,RMVar_hsa_circ_112797,RMVar_hsa_circ_95915,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326,RMVar_hsa_circ_268813,RMVar_hsa_circ_247200,RMVar_hsa_circ_247201,RMVar_hsa_circ_247203,RMVar_hsa_circ_247202 74589 RMVar_ID_74589 Human_SNP_ID_332786318 m1A Human chr7 - 100886336 100886336 100886336 AGCTTGGCCGCCAGCTTGATGTCGTTGCGCACAATCTGCTTGTGCTGGGTGATGCCGTTGATGTT AGCTTGGCCGCCAGCTTGATGTCGTTGCGCACGATCTGCTTGTGCTGGGTGATGCCGTTGATGTT T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100886290..100886455 26863196 MeRIP-seq:(Medium) rs1404026276 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 74590 RMVar_ID_74590 Human_SNP_ID_332786319 m1A Human chr7 - 100886336 100886336 100886336 AGCTTGGCCGCCAGCTTGATGTCGTTGCGCACAATCTGCTTGTGCTGGGTGATGCCGTTGATGTT AGCTTGGCCGCCAGCTTGATGTCGTTGCGCACCATCTGCTTGTGCTGGGTGATGCCGTTGATGTT T G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100886290..100886455 26863196 MeRIP-seq:(Medium) rs1404026276 Functional Loss SNV dbSNP153 33..33 33 - - - 74591 RMVar_ID_74591 Human_SNP_ID_332787059 m1A Human chr7 + 100888067 100888067 100888067 CGTGTTGTACTCCCCCCAGGTTTGACCCCAGGACTCCCCTACCCACACCAGACTCCCCAGGGCCT CGTGTTGTACTCCCCCCAGGTTTGACCCCAGGTCTCCCCTACCCACACCAGACTCCCCAGGGCCT A T SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100888051..100888075 26863196 MeRIP-seq:(Medium) rs1010301297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83181,Human_RBP_ID_1049529,Human_RBP_ID_3972311,Human_RBP_ID_5123075,Human_RBP_ID_7666691,Human_RBP_ID_9309967,Human_RBP_ID_15946296,Human_RBP_ID_18087369,Human_RBP_ID_18872637,Human_RBP_ID_22111059,Human_RBP_ID_23070024,Human_RBP_ID_24180268,Human_RBP_ID_26131139,Human_RBP_ID_27830614 Human_Splice_Rec_901509,Human_Splice_Rec_901548,Human_Splice_Rec_901549,Human_Splice_Rec_901585,Human_Splice_Rec_901630,Human_Splice_Rec_901631,Human_Splice_Rec_901675,Human_Splice_Rec_901695 Human_miRNA_ID_2039653,Human_miRNA_ID_3018635 RMVar_hsa_circ_34585,RMVar_hsa_circ_111923,RMVar_hsa_circ_247197,RMVar_hsa_circ_112797,RMVar_hsa_circ_95915,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326,RMVar_hsa_circ_247200,RMVar_hsa_circ_247201,RMVar_hsa_circ_247202,RMVar_hsa_circ_103465,RMVar_hsa_circ_247204,RMVar_hsa_circ_84464,RMVar_hsa_circ_85025,RMVar_hsa_circ_101490,RMVar_hsa_circ_247206,RMVar_hsa_circ_92040,RMVar_hsa_circ_247207,RMVar_hsa_circ_247208,RMVar_hsa_circ_24126,RMVar_hsa_circ_247210 74592 RMVar_ID_74592 Human_SNP_ID_332787289 m1A Human chr7 + 100888507 100888507 100888507 ATGGTTCGTGGAGACCCAAGGGCCATTGTGGAATATCGGGACCTGGATGCCCCAGACGATGTTGA ATGGTTCGTGGAGACCCAAGGGCCATTGTGGAGTATCGGGACCTGGATGCCCCAGACGATGTTGA A G SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100888323..100888614 32194978 MeRIP-seq:(Medium) rs370307936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83183,Human_RBP_ID_671588,Human_RBP_ID_1049532,Human_RBP_ID_1679531,Human_RBP_ID_2031765,Human_RBP_ID_3823694,Human_RBP_ID_8652705,Human_RBP_ID_8906523,Human_RBP_ID_15946299,Human_RBP_ID_18872641,Human_RBP_ID_23070029,Human_RBP_ID_23215873 Human_Splice_Rec_901512,Human_Splice_Rec_901552,Human_Splice_Rec_901588,Human_Splice_Rec_901634,Human_Splice_Rec_901678,Human_Splice_Rec_901696,Human_Splice_Rec_901698 RMVar_hsa_circ_111923,RMVar_hsa_circ_247197,RMVar_hsa_circ_112797,RMVar_hsa_circ_95915,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326,RMVar_hsa_circ_247201,RMVar_hsa_circ_247202,RMVar_hsa_circ_103465,RMVar_hsa_circ_247204,RMVar_hsa_circ_84464,RMVar_hsa_circ_85025,RMVar_hsa_circ_101490,RMVar_hsa_circ_247206,RMVar_hsa_circ_92040,RMVar_hsa_circ_247207,RMVar_hsa_circ_247208,RMVar_hsa_circ_247210,RMVar_hsa_circ_247211,RMVar_hsa_circ_102542 74593 RMVar_ID_74593 Human_SNP_ID_332787322 m1A Human chr7 - 100888589 100888589 100888589 AAAATTCTCAGAGCTTCATAGGACAAGGTAGTACAAGTATGGATGATACAGGACTGAGGAACGGG AAAATTCTCAGAGCTTCATAGGACAAGGTAGTGCAAGTATGGATGATACAGGACTGAGGAACGGG T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100888538..100888609 26863196 MeRIP-seq:(Medium) rs1014503997 Functional Loss SNV dbSNP153 33..33 33 - - - 74594 RMVar_ID_74594 Human_SNP_ID_332787701 m1A Human chr7 - 100889176 100889173 100889176 CTCTGCCTCGCTCACTTCGGAGGGCCCCAGGGACGCCTCTGCCACGTACCCCGGGGAGTGGGGCT CTCTGCCTCGCTCACTTCGGAGGGCCCCAGGG___CCTCTGCCACGTACCCCGGGGAGTGGGGCT GCGT G UFSP1 Ensembl:ENSG00000176125 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100888921..100889270 26863196 MeRIP-seq:(Medium) rs779492277 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_254499,Human_RBP_ID_18087374 74595 RMVar_ID_74595 Human_SNP_ID_332787877 m1A Human chr7 + 100889574 100889574 100889574 CTCCTAGCGGCGCGGAGCGACCTCAGGCTCCAACACTTCCTTTCGGCTCCGGGTCTTGGGCCAGC CTCCTAGCGGCGCGGAGCGACCTCAGGCTCCAGCACTTCCTTTCGGCTCCGGGTCTTGGGCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100889537..100889656 26863196 MeRIP-seq:(Medium) rs908360582 Functional Loss SNV dbSNP153 33..33 33 - - - 74596 RMVar_ID_74596 Human_SNP_ID_332787881 m1A Human chr7 - 100889589 100889589 100889589 GCCGGTCCTGCGGCAGCTGGCCCAAGACCCGGAGCCGAAAGGAAGTGTTGGAGCCTGAGGTCGCT GCCGGTCCTGCGGCAGCTGGCCCAAGACCCGGCGCCGAAAGGAAGTGTTGGAGCCTGAGGTCGCT T G UFSP1 Ensembl:ENSG00000176125 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100889550..100889647 26863196 MeRIP-seq:(Medium) rs936419404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956559 74597 RMVar_ID_74597 Human_SNP_ID_332788401 m1A Human chr7 + 100890862 100890862 100890862 CAGTGTGAGTCTCTCGGTTTGAGGAGGAAGGGAGCACTAGGTCTGAGATCCCTGAGTGGGGCCCT CAGTGTGAGTCTCTCGGTTTGAGGAGGAAGGGGGCACTAGGTCTGAGATCCCTGAGTGGGGCCCT A G AChE-AS RNACentral:URS00007CCDDD antisense RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100890838..100890939 26863196 MeRIP-seq:(Medium) rs1455284162 Functional Loss SNV dbSNP153 33..33 33 - - - 74598 RMVar_ID_74598 Human_SNP_ID_332855879 m1A Human chr7 + 101087061 101087061 101087061 GTAGCACTGACATTTTTACGTTTGCTGGATGTACACACGGAAGTGGAGGAGGAGGAGGAGAAGGA GTAGCACTGACATTTTTACGTTTGCTGGATGTGCACACGGAAGTGGAGGAGGAGGAGGAGAAGGA A G TRIM56 Ensembl:ENSG00000169871 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101087011..101087107 26863196 MeRIP-seq:(Medium) rs879805176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267864 Human_Splice_Rec_901980,Human_Splice_Rec_901984 RMVar_hsa_circ_7803 74599 RMVar_ID_74599 Human_SNP_ID_332856308 m1A Human chr7 - 101088071 101088071 101088071 CGGAGGACGCCCTCAGCCGCCTCCTCCACCTGAGTCCCCACCCGGGCCGCCTGCTCCCGCAGCCG CGGAGGACGCCCTCAGCCGCCTCCTCCACCTGGGTCCCCACCCGGGCCGCCTGCTCCCGCAGCCG T C RF00017-6494 RNACentral:URS0000968BD0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101087908..101088200;chr7:101087826..101088241;chr7:101087941..101088250 26863196 MeRIP-seq:(Medium) rs764840826 Functional Loss SNV dbSNP153 33..33 33 - - - 74600 RMVar_ID_74600 Human_SNP_ID_332867543 m1A Human chr7 - 101128573 101128573 101128573 AGCTGGAGCATGGCCAACACCGAGGCCACCCCATAGGGTGAGAAAACCACGTTGCGGTCCTTGGA AGCTGGAGCATGGCCAACACCGAGGCCACCCCGTAGGGTGAGAAAACCACGTTGCGGTCCTTGGA T C lnc-VGF-4,RF00017-6494 RNACentral:URS0000D5DC07,RNACentral:URS0000968BD0 lincRNA,SRP RNA exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101128526..101128600 32194978 MeRIP-seq:(Medium) rs376485687 Functional Loss SNV dbSNP153 33..33 33 - - - 74601 RMVar_ID_74601 Human_SNP_ID_332868325 m1A Human chr7 - 101130453 101130453 101130453 ATCCTTGTTCCATGGCCCCATGAGCTCCTTGTACAGATGCCGGAGGGCGGGGGCCATGCCCTTGT ATCCTTGTTCCATGGCCCCATGAGCTCCTTGTGCAGATGCCGGAGGGCGGGGGCCATGCCCTTGT T C lnc-VGF-4,RF00017-6494 RNACentral:URS0000D5DC07,RNACentral:URS0000968BD0 lincRNA,SRP RNA exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101130451..101130525 32194978 MeRIP-seq:(Medium) rs748629078 Functional Loss SNV dbSNP153 33..33 33 - - - 74602 RMVar_ID_74602 Human_SNP_ID_332869273 m1A Human chr7 - 101133678 101133678 101133678 GGCGTGGTGAACTCAGCTGTGAAGACGACAAGATGGTTCGTTGGAAATGGCTCCAGCTCTCGCTG GGCGTGGTGAACTCAGCTGTGAAGACGACAAGGTGGTTCGTTGGAAATGGCTCCAGCTCTCGCTG T C RF00017-6494 RNACentral:URS0000968BD0 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101133676..101133725 32194978 MeRIP-seq:(Medium) rs1422361395 Functional Loss SNV dbSNP153 33..33 33 - - - 74603 RMVar_ID_74603 Human_SNP_ID_332869274 m1A Human chr7 - 101133678 101133678 101133678 GGCGTGGTGAACTCAGCTGTGAAGACGACAAGATGGTTCGTTGGAAATGGCTCCAGCTCTCGCTG GGCGTGGTGAACTCAGCTGTGAAGACGACAAGCTGGTTCGTTGGAAATGGCTCCAGCTCTCGCTG T G RF00017-6494 RNACentral:URS0000968BD0 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101133676..101133725 32194978 MeRIP-seq:(Medium) rs1422361395 Functional Loss SNV dbSNP153 33..33 33 - - - 74604 RMVar_ID_74604 Human_SNP_ID_332875633 m1A Human chr7 + 101154499 101154499 101154499 GGCGCCTACGGTGGCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAA GGCGCCTACGGTGGCCGAAGTGGGACGCGCCGGGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAA A G AP1S1 Ensembl:ENSG00000106367 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:101154481..101154608;chr7:101154476..101154550;chr7:101154401..101154686;chr7:101154424..101154684 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1234738293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956562 Human_Splice_Rec_902009,Human_Splice_Rec_902017,Human_Splice_Rec_902025 74605 RMVar_ID_74605 Human_SNP_ID_332875634 m1A Human chr7 + 101154499 101154499 101154499 GGCGCCTACGGTGGCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAA GGCGCCTACGGTGGCCGAAGTGGGACGCGCCGTGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAA A T AP1S1 Ensembl:ENSG00000106367 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:101154481..101154608;chr7:101154476..101154550;chr7:101154401..101154686;chr7:101154424..101154684 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1234738293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956562 Human_Splice_Rec_902009,Human_Splice_Rec_902017,Human_Splice_Rec_902025 74606 RMVar_ID_74606 Human_SNP_ID_332875639 m1A Human chr7 + 101154505 101154505 101154505 TACGGTGGCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAAGAGGGA TACGGTGGCCGAAGTGGGACGCGCCGAGCCGGCGGCTGCAGGATGGTAGGCTGTGCGAAGAGGGA A C AP1S1 Ensembl:ENSG00000106367 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101154426..101154652 26863196 MeRIP-seq:(Medium) rs559897692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956562 Human_Splice_Rec_902009,Human_Splice_Rec_902017,Human_Splice_Rec_902025 74607 RMVar_ID_74607 Human_SNP_ID_332875640 m1A Human chr7 + 101154505 101154505 101154505 TACGGTGGCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAAGAGGGA TACGGTGGCCGAAGTGGGACGCGCCGAGCCGGGGGCTGCAGGATGGTAGGCTGTGCGAAGAGGGA A G AP1S1 Ensembl:ENSG00000106367 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101154426..101154652 26863196 MeRIP-seq:(Medium) rs559897692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956562 Human_Splice_Rec_902009,Human_Splice_Rec_902017,Human_Splice_Rec_902025 74608 RMVar_ID_74608 Human_SNP_ID_332875642 m1A Human chr7 - 101154509 101154509 101154509 CCCCTCCCTCTTCGCACAGCCTACCATCCTGCAGCCTCCGGCTCGGCGCGTCCCACTTCGGCCAC CCCCTCCCTCTTCGCACAGCCTACCATCCTGCTGCCTCCGGCTCGGCGCGTCCCACTTCGGCCAC T A RF00017-6494 RNACentral:URS0000968BD0 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:101154460..101154622 26863196 MeRIP-seq:(Medium) rs373167203 Functional Loss SNV dbSNP153 33..33 33 - - - 74609 RMVar_ID_74609 Human_SNP_ID_332875646 m1A Human chr7 + 101154512 101154512 101154512 GCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCAGGATGGTAGGCTGTGCGAAGAGGGAGGGGAGG GCCGAAGTGGGACGCGCCGAGCCGGAGGCTGCGGGATGGTAGGCTGTGCGAAGAGGGAGGGGAGG A G AP1S1 Ensembl:ENSG00000106367 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:101154485..101154611 26863196 MeRIP-seq:(Medium) rs1199610966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956562 Human_Splice_Rec_902009,Human_Splice_Rec_902017,Human_Splice_Rec_902025 74610 RMVar_ID_74610 Human_SNP_ID_332875759 m1A Human chr7 + 101154747 101154747 101154747 GGCGCATTTGCAGGGCGAGCGGGGGCTGACGAAGGGGCGGCGGGGCCGTCCCGAGCCGGGAGGGG GGCGCATTTGCAGGGCGAGCGGGGGCTGACGAGGGGGCGGCGGGGCCGTCCCGAGCCGGGAGGGG A G AP1S1 Ensembl:ENSG00000106367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101154745..101154831 26863196 MeRIP-seq:(Medium) rs1055747929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13942,Human_RBP_ID_8218463,Human_RBP_ID_9439836,Human_RBP_ID_21992530 74611 RMVar_ID_74611 Human_SNP_ID_332876224 m1A Human chr7 - 101156556 101156556 101156556 GGGGATGGGAGGGCAGAACCGAGGGTAACCACACATTCCCCAAACTTATCTCCAGCTAATTCTTC GGGGATGGGAGGGCAGAACCGAGGGTAACCACGCATTCCCCAAACTTATCTCCAGCTAATTCTTC T C RF00017-6494 RNACentral:URS0000968BD0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101156554..101156775 26863196 MeRIP-seq:(Medium) rs536749580 Functional Loss SNV dbSNP153 33..33 33 - - - 74612 RMVar_ID_74612 Human_SNP_ID_332876945 m1A Human chr7 + 101159187 101159184 101159187 AGTGTGCTGAAAGCCATCGAGCAGGCTGACCTACTGCAAGAGGTACGGGCCAGGGACAGTGAGGA AGTGTGCTGAAAGCCATCGAGCAGGCTGAC___CTGCAAGAGGTACGGGCCAGGGACAGTGAGGA CCTA C AP1S1 Ensembl:ENSG00000106367 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101159060..101160695 26863196 MeRIP-seq:(Medium) rs1306139133 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_794957,Human_RBP_ID_9201466,Human_RBP_ID_19021341 Human_Splice_Rec_902015,Human_Splice_Rec_902023,Human_Splice_Rec_902031,Human_Splice_Rec_902041,Human_Splice_Rec_902049 RMVar_hsa_circ_9269 74613 RMVar_ID_74613 Human_SNP_ID_332878319 m1A Human chr7 - 101163182 101163182 101163182 CACCCTTTCCCCAACTACATCCGGCCGCGGACACTGCAGCCGCCCTCGGCCTTGCGCCGCCGCCA CACCCTTTCCCCAACTACATCCGGCCGCGGACTCTGCAGCCGCCCTCGGCCTTGCGCCGCCGCCA T A VGF Ensembl:ENSG00000128564 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101162852..101163660 26863196 MeRIP-seq:(Medium) rs1248296104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22775059,Human_RBP_ID_27527434 74614 RMVar_ID_74614 Human_SNP_ID_332878516 m1A Human chr7 - 101163516 101163516 101163516 CGAGGGGACAGAGGAGGGCGGGGAGGAGGAGGACGACGAGGAGATGGATCCGCAGACGATCGACA CGAGGGGACAGAGGAGGGCGGGGAGGAGGAGGGCGACGAGGAGATGGATCCGCAGACGATCGACA T C VGF Ensembl:ENSG00000128564 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:101163388..101163885 26863196 MeRIP-seq:(Medium) rs1188139410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247229 74615 RMVar_ID_74615 Human_SNP_ID_332891529 m1A Human chr7 + 101206402 101206400 101206402 GGAGTGCCCAGCCCTTCCTCGGGGAGGAGATCACACAGTCGTAGCGCAGGAAGCGGCAGCCACCT GGAGTGCCCAGCCCTTCCTCGGGGAGGAGAT__CACAGTCGTAGCGCAGGAAGCGGCAGCCACCT TCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101206351..101207688 32194978 MeRIP-seq:(Medium) rs1268576956 Functional Loss DEL dbSNP153 32..33 33 - - - 74616 RMVar_ID_74616 Human_SNP_ID_332891698 m1A Human chr7 + 101206809 101206809 101206809 ACCTCATAGTCCAGGCCCTTGTGGTTGAGGGCAACGTTGAGGGTGAAGGTGGATGAGTCGTGGTG ACCTCATAGTCCAGGCCCTTGTGGTTGAGGGCGACGTTGAGGGTGAAGGTGGATGAGTCGTGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:101206075..101206816 32194978 MeRIP-seq:(Medium) rs1208101950 Functional Loss SNV dbSNP153 33..33 33 - - - 74617 RMVar_ID_74617 Human_SNP_ID_332892353 m1A Human chr7 - 101208817 101208817 101208817 AGGGCCTGGGCGAGGAGGGCAGAGGCCTTCCCAGAGGAGGAGGTGCAGGATCTGGTAAACAAACA AGGGCCTGGGCGAGGAGGGCAGAGGCCTTCCCGGAGGAGGAGGTGCAGGATCTGGTAAACAAACA T C PLOD3 Ensembl:ENSG00000106397 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101208767..101208853 26863196 MeRIP-seq:(Medium) rs749925886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843290,Human_RBP_ID_952682,Human_RBP_ID_5401687,Human_RBP_ID_19135335,Human_RBP_ID_22366651,Human_RBP_ID_22687197 RMVar_hsa_circ_84976,RMVar_hsa_circ_247234,RMVar_hsa_circ_87798,RMVar_hsa_circ_265562,RMVar_hsa_circ_247235 74618 RMVar_ID_74618 Human_SNP_ID_332892395 m1A Human chr7 - 101208919 101208919 101208919 CCGGACGTGTACTGGTTCCCACTGCTGTCAGAACAAATGTGTGATGAGCTGGTGGCAGAGATGGA CCGGACGTGTACTGGTTCCCACTGCTGTCAGATCAAATGTGTGATGAGCTGGTGGCAGAGATGGA T A PLOD3 Ensembl:ENSG00000106397 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101208854..101209868 32194978 MeRIP-seq:(Medium) rs372579198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83907,Human_RBP_ID_19021345,Human_RBP_ID_26356879 Human_Splice_Rec_902124,Human_Splice_Rec_902125,Human_Splice_Rec_902158,Human_Splice_Rec_902159,Human_Splice_Rec_902166 Human_miRNA_ID_2539444 RMVar_hsa_circ_96470,RMVar_hsa_circ_84976,RMVar_hsa_circ_247234,RMVar_hsa_circ_87798,RMVar_hsa_circ_265562,RMVar_hsa_circ_372441,RMVar_hsa_circ_247235,RMVar_hsa_circ_104336,RMVar_hsa_circ_247236,RMVar_hsa_circ_247238,RMVar_hsa_circ_80285,RMVar_hsa_circ_247239,RMVar_hsa_circ_247237 74619 RMVar_ID_74619 Human_SNP_ID_332892396 m1A Human chr7 - 101208919 101208919 101208919 CCGGACGTGTACTGGTTCCCACTGCTGTCAGAACAAATGTGTGATGAGCTGGTGGCAGAGATGGA CCGGACGTGTACTGGTTCCCACTGCTGTCAGAGCAAATGTGTGATGAGCTGGTGGCAGAGATGGA T C PLOD3 Ensembl:ENSG00000106397 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:101208854..101209868 32194978 MeRIP-seq:(Medium) rs372579198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83907,Human_RBP_ID_19021345,Human_RBP_ID_26356879 Human_Splice_Rec_902124,Human_Splice_Rec_902125,Human_Splice_Rec_902158,Human_Splice_Rec_902159,Human_Splice_Rec_902166 Human_miRNA_ID_2539444 RMVar_hsa_circ_96470,RMVar_hsa_circ_84976,RMVar_hsa_circ_247234,RMVar_hsa_circ_87798,RMVar_hsa_circ_265562,RMVar_hsa_circ_372441,RMVar_hsa_circ_247235,RMVar_hsa_circ_104336,RMVar_hsa_circ_247236,RMVar_hsa_circ_247238,RMVar_hsa_circ_80285,RMVar_hsa_circ_247239,RMVar_hsa_circ_247237 74620 RMVar_ID_74620 Human_SNP_ID_332895110 m1A Human chr7 - 101216487 101216487 101216487 GGGGGTGATGTGGCTCGAACAGTTGGTGGAGGACAGAAGGTCCGGTGGTTAAAGAAGGAAATGGA GGGGGTGATGTGGCTCGAACAGTTGGTGGAGGTCAGAAGGTCCGGTGGTTAAAGAAGGAAATGGA T A PLOD3 Ensembl:ENSG00000106397 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101216305..101216568;chr7:101216305..101216557;chr7:101216301..101216550;chr7:101216319..101216572 26863196 MeRIP-seq:(Medium) rs1469143994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955942,Human_RBP_ID_9337924,Human_RBP_ID_22463715 Human_Splice_Rec_902132,Human_Splice_Rec_902133,Human_Splice_Rec_902200,Human_Splice_Rec_902201,Human_Splice_Rec_902225,Human_Splice_Rec_902236,Human_Splice_Rec_902237,Human_Splice_Rec_902244,Human_Splice_Rec_902245,Human_Splice_Rec_902254 RMVar_hsa_circ_20835 74621 RMVar_ID_74621 Human_SNP_ID_332895111 m1A Human chr7 - 101216487 101216487 101216487 GGGGGTGATGTGGCTCGAACAGTTGGTGGAGGACAGAAGGTCCGGTGGTTAAAGAAGGAAATGGA GGGGGTGATGTGGCTCGAACAGTTGGTGGAGGGCAGAAGGTCCGGTGGTTAAAGAAGGAAATGGA T C PLOD3 Ensembl:ENSG00000106397 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101216305..101216568;chr7:101216305..101216557;chr7:101216301..101216550;chr7:101216319..101216572 26863196 MeRIP-seq:(Medium) rs1469143994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955942,Human_RBP_ID_9337924,Human_RBP_ID_22463715 Human_Splice_Rec_902132,Human_Splice_Rec_902133,Human_Splice_Rec_902200,Human_Splice_Rec_902201,Human_Splice_Rec_902225,Human_Splice_Rec_902236,Human_Splice_Rec_902237,Human_Splice_Rec_902244,Human_Splice_Rec_902245,Human_Splice_Rec_902254 RMVar_hsa_circ_20835 74622 RMVar_ID_74622 Human_SNP_ID_332895407 m1A Human chr7 - 101217277 101217277 101217277 AGGATCCTGGGTGCTGTCTGGGCCCGCTCCCCACCATGACCTCCTCGGGGCCTGGACCCCGGTTC AGGATCCTGGGTGCTGTCTGGGCCCGCTCCCCGCCATGACCTCCTCGGGGCCTGGACCCCGGTTC T C PLOD3 Ensembl:ENSG00000106397 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101217229..101217575;chr7:101217226..101217346 26863196 MeRIP-seq:(Medium) rs1232654133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955943,Human_RBP_ID_22463718 74623 RMVar_ID_74623 Human_SNP_ID_332895743 m1A Human chr7 - 101218219 101218219 101218219 AGGGGAAGGGGGCGAACCGCGGGGGCTCACATACCCGAAGTTTTCTTCTCCACCATTGGCACAAC AGGGGAAGGGGGCGAACCGCGGGGGCTCACATGCCCGAAGTTTTCTTCTCCACCATTGGCACAAC T C PLOD3 Ensembl:ENSG00000106397 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101218176..101218272;chr7:101218151..101218276;chr7:101218201..101218306;chr7:101218176..101218285 26863196 MeRIP-seq:(Medium) rs767554742 Functional Loss SNV dbSNP153 33..33 33 - - - 74624 RMVar_ID_74624 Human_SNP_ID_332896665 m1A Human chr7 - 101221660 101221660 101221660 TCTATGGAGGTGGCTGGCCCTCTTCTCTGCTCAGTCTATGCACTCTTCCTGGGATTTTGACTCCA TCTATGGAGGTGGCTGGCCCTCTTCTCTGCTCCGTCTATGCACTCTTCCTGGGATTTTGACTCCA T G RF00017-1028 RNACentral:URS00008FFE84 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101221657..101222564 26863196 MeRIP-seq:(Medium) rs1036811626 Functional Loss SNV dbSNP153 33..33 33 - - - 74625 RMVar_ID_74625 Human_SNP_ID_332897160 m1A Human chr7 + 101223483 101223483 101223483 AGCAACGGATCACCCTTGACCCCTAGGAAAGAAAAAGAAGAAAACCCGAGGTGATCATTTTAAAC AGCAACGGATCACCCTTGACCCCTAGGAAAGAGAAAGAAGAAAACCCGAGGTGATCATTTTAAAC A G ZNHIT1 Ensembl:ENSG00000106400 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:101223476..101223575 32194978 MeRIP-seq:(Medium) rs142789038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22774448 Human_Splice_Rec_902260,Human_Splice_Rec_902261,Human_Splice_Rec_902270,Human_Splice_Rec_902271,Human_Splice_Rec_902278,Human_Splice_Rec_902279,Human_Splice_Rec_902284,Human_Splice_Rec_902285 RMVar_hsa_circ_94493,RMVar_hsa_circ_115169,RMVar_hsa_circ_247243,RMVar_hsa_circ_84837,RMVar_hsa_circ_247244,RMVar_hsa_circ_247245,RMVar_hsa_circ_247246 74626 RMVar_ID_74626 Human_SNP_ID_332901991 m1A Human chr7 - 101239842 101239842 101239842 GGCATGGCCCTGGGTGTGGCGGGACTGGCCGGACTCATCGGACTTGCTGTGTCCAAGTCCAAATC GGCATGGCCCTGGGTGTGGCGGGACTGGCCGGGCTCATCGGACTTGCTGTGTCCAAGTCCAAATC T C FIS1 Ensembl:ENSG00000214253 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101239795..101239943 26863196 MeRIP-seq:(Medium) rs749957366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671745,Human_RBP_ID_1049564,Human_RBP_ID_3972318,Human_RBP_ID_17665104,Human_RBP_ID_18872721,Human_RBP_ID_19020017,Human_RBP_ID_22464196,Human_RBP_ID_23080576,Human_RBP_ID_24180397,Human_RBP_ID_27103142 Human_Splice_Rec_902352,Human_Splice_Rec_902360,Human_Splice_Rec_902366,Human_Splice_Rec_902372,Human_Splice_Rec_902378,Human_Splice_Rec_902382,Human_Splice_Rec_902390,Human_Splice_Rec_902396,Human_Splice_Rec_902402 RMVar_hsa_circ_77457,RMVar_hsa_circ_89647,RMVar_hsa_circ_80094,RMVar_hsa_circ_247250,RMVar_hsa_circ_247251,RMVar_hsa_circ_247249 74627 RMVar_ID_74627 Human_SNP_ID_332902133 m1A Human chr7 - 101240195 101240195 101240195 GTACGTCCGCGGGTTGCTGCAGACAGAGCCCCAGAACAACCAGGCCAAGGAACTGGAGCGGCTCA GTACGTCCGCGGGTTGCTGCAGACAGAGCCCCGGAACAACCAGGCCAAGGAACTGGAGCGGCTCA T C FIS1 Ensembl:ENSG00000214253 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:101240099..101240264;chr7:101240126..101240200 26863196 MeRIP-seq:(Medium) rs1162946764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671747,Human_RBP_ID_5123085,Human_RBP_ID_19020018,Human_RBP_ID_27350375 Human_Splice_Rec_902350,Human_Splice_Rec_902351,Human_Splice_Rec_902358,Human_Splice_Rec_902359,Human_Splice_Rec_902364,Human_Splice_Rec_902365,Human_Splice_Rec_902370,Human_Splice_Rec_902371,Human_Splice_Rec_902376,Human_Splice_Rec_902377,Human_Splice_Rec_902380,Human_Splice_Rec_902381,Human_Splice_Rec_902388,Human_Splice_Rec_902389,Human_Splice_Rec_902400,Human_Splice_Rec_902401 Human_miRNA_ID_2217548 RMVar_hsa_circ_77457,RMVar_hsa_circ_89647,RMVar_hsa_circ_80094,RMVar_hsa_circ_247250,RMVar_hsa_circ_247251,RMVar_hsa_circ_247249 74628 RMVar_ID_74628 Human_SNP_ID_332902394 m1A Human chr7 - 101240906 101240906 101240906 CATTTCTCACCCTCTTCTCTGCCCCTCCCCAGAGCTGCTGCCCAAAGGGAGCAAGGAGGAACAGC CATTTCTCACCCTCTTCTCTGCCCCTCCCCAGCGCTGCTGCCCAAAGGGAGCAAGGAGGAACAGC T G FIS1 Ensembl:ENSG00000214253 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101240876..101240925 26863196 MeRIP-seq:(Medium) rs1562907737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671750,Human_RBP_ID_18108104 Human_Splice_Rec_902348,Human_Splice_Rec_902349,Human_Splice_Rec_902356,Human_Splice_Rec_902357,Human_Splice_Rec_902362,Human_Splice_Rec_902363,Human_Splice_Rec_902368,Human_Splice_Rec_902369,Human_Splice_Rec_902374,Human_Splice_Rec_902375,Human_Splice_Rec_902379,Human_Splice_Rec_902386,Human_Splice_Rec_902387,Human_Splice_Rec_902394,Human_Splice_Rec_902395,Human_Splice_Rec_902398,Human_Splice_Rec_902399 Human_miRNA_ID_2192897,Human_miRNA_ID_2207106 RMVar_hsa_circ_77457,RMVar_hsa_circ_89647,RMVar_hsa_circ_80094,RMVar_hsa_circ_247250,RMVar_hsa_circ_247251,RMVar_hsa_circ_247249 74629 RMVar_ID_74629 Human_SNP_ID_332903630 m1A Human chr7 + 101245029 101245029 101245029 GCCTCCATGGCCACTGCCCCCGCGAGCCTCACACTACAGTCTACTGTGCCACAGTCTCCATGGCC GCCTCCATGGCCACTGCCCCCGCGAGCCTCACCCTACAGTCTACTGTGCCACAGTCTCCATGGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101244889..101245100 26863196 MeRIP-seq:(Medium) rs1394259092 Functional Loss SNV dbSNP153 33..33 33 - - - 74630 RMVar_ID_74630 Human_SNP_ID_332905673 m1A Human chr7 - 101251978 101251971 101251978 GATCTGTTGACCGGGCATGGTGGGTAGAAGGAACGCTCCGAGCAGAAGAAAAGTGGCTGTCGTGA GATCTGTTGACCGGGCATGGTGGGTAGAAGGA_______GAGCAGAAGAAAAGTGGCTGTCGTGA CGGAGCGT C FIS1 Ensembl:ENSG00000214253 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101251859..101252025 26863196 MeRIP-seq:(Medium) rs1184076302 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_671759,Human_RBP_ID_24180413 Human_Splice_Rec_902367,Human_Splice_Rec_902383,Human_Splice_Rec_902391 RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 74631 RMVar_ID_74631 Human_SNP_ID_332905700 m1A Human chr7 - 101252077 101252077 101252077 CCTAGGAGCCGAAGGGACGGGAGGCCGCGTAGAGGAGGGGACCGTCCCCGAGCCTCGCCGAGCCT CCTAGGAGCCGAAGGGACGGGAGGCCGCGTAGCGGAGGGGACCGTCCCCGAGCCTCGCCGAGCCT T G FIS1 Ensembl:ENSG00000214253 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101252027..101252158 26863196 MeRIP-seq:(Medium) rs1166601891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 74632 RMVar_ID_74632 Human_SNP_ID_332921522 m1A Human chr7 + 101308350 101308350 101308350 GGACTACAGGCTCAAGATGGCCTGGTAGATGCAGCCGGCACGCACCTCTCCTCTGACGGGAACCG GGACTACAGGCTCAAGATGGCCTGGTAGATGCCGCCGGCACGCACCTCTCCTCTGACGGGAACCG A C EMSLR Ensembl:ENSG00000232445 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:101308301..101308525;chr7:101308301..101308533;chr7:101308301..101308597 26863196 MeRIP-seq:(Medium) rs1385472283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1329346 74633 RMVar_ID_74633 Human_SNP_ID_332921532 m1A Human chr7 + 101308373 101308373 101308373 GGTAGATGCAGCCGGCACGCACCTCTCCTCTGACGGGAACCGAAGGAGCCGGTAGGTTTTCACAC GGTAGATGCAGCCGGCACGCACCTCTCCTCTGGCGGGAACCGAAGGAGCCGGTAGGTTTTCACAC A G EMSLR Ensembl:ENSG00000232445 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101308323..101308484 26863196 MeRIP-seq:(Medium) rs919415212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4918587,Human_RBP_ID_15946874 74634 RMVar_ID_74634 Human_SNP_ID_332921826 m1A Human chr7 + 101309274 101309274 101309274 GGTCGGGGGGCTTCTCCCTGTGTGCGGCGACGAGAGAGTGTAGAAATAAAGACACAAGACAAAGG GGTCGGGGGGCTTCTCCCTGTGTGCGGCGACGGGAGAGTGTAGAAATAAAGACACAAGACAAAGG A G EMSLR Ensembl:ENSG00000232445 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101309271..101309374 26863196 MeRIP-seq:(Medium) rs1264289144 Functional Loss SNV dbSNP153 33..33 33 - - - 74635 RMVar_ID_74635 Human_SNP_ID_332925211 m1A Human chr7 - 101321608 101321608 101321608 CGGGGAGCAGGCCTCGGGGCCTGGGCGAGCGCAGGTCCCCACCCGTCTGATCTGCGGCTTGCTCC CGGGGAGCAGGCCTCGGGGCCTGGGCGAGCGCGGGTCCCCACCCGTCTGATCTGCGGCTTGCTCC T C IFT22 Ensembl:ENSG00000128581 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:101321600..101321732 26863196 MeRIP-seq:(Medium) rs749305259 Functional Loss SNV dbSNP153 33..33 33 - - - 74636 RMVar_ID_74636 Human_SNP_ID_332925273 m1A Human chr7 + 101321748 101321748 101321748 CCGCCGCGGCTTAGCCGGCCGGAGCCCACGGGAGGCGGCGCGTCAGGACGGAGCTCTACTTGGCC CCGCCGCGGCTTAGCCGGCCGGAGCCCACGGGGGGCGGCGCGTCAGGACGGAGCTCTACTTGGCC A G RF00017-4633 RNACentral:URS00009644F0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:101321628..101321752;chr7:101321621..101321747;chr7:101321630..101321754 26863196 MeRIP-seq:(Medium) rs1044871082 Functional Loss SNV dbSNP153 33..33 33 - - - 74637 RMVar_ID_74637 Human_SNP_ID_332925274 m1A Human chr7 + 101321748 101321748 101321748 CCGCCGCGGCTTAGCCGGCCGGAGCCCACGGGAGGCGGCGCGTCAGGACGGAGCTCTACTTGGCC CCGCCGCGGCTTAGCCGGCCGGAGCCCACGGGTGGCGGCGCGTCAGGACGGAGCTCTACTTGGCC A T RF00017-4633 RNACentral:URS00009644F0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:101321628..101321752;chr7:101321621..101321747;chr7:101321630..101321754 26863196 MeRIP-seq:(Medium) rs1044871082 Functional Loss SNV dbSNP153 33..33 33 - - - 74638 RMVar_ID_74638 Human_SNP_ID_332989825 m1A Human chr7 - 101556846 101556846 101556846 ATCTATGCATCTATCCATTCATTCACTCATTTACCCATCCATCTATCATCCATCCATCCATCCAT ATCTATGCATCTATCCATTCATTCACTCATTTCCCCATCCATCTATCATCCATCCATCCATCCAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101556429..101556893 26863196 MeRIP-seq:(Medium) rs996549040 Functional Loss SNV dbSNP153 33..33 33 - - - 74639 RMVar_ID_74639 Human_SNP_ID_333056193 m1A Human chr7 + 101816000 101816000 101816000 GGCGGCTCCTGAACTCCAGCCCCCTCTCTATCAGCCGCTCACTCCGTCTCAATATGTCTCAAGAT GGCGGCTCCTGAACTCCAGCCCCCTCTCTATCTGCCGCTCACTCCGTCTCAATATGTCTCAAGAT A T CUX1 Ensembl:ENSG00000257923 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:101815833..101816005 26863196 MeRIP-seq:(Medium) rs368174106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671800 Human_Splice_Rec_902567,Human_Splice_Rec_902611,Human_Splice_Rec_902653,Human_Splice_Rec_902695,Human_Splice_Rec_902707,Human_Splice_Rec_902751,Human_Splice_Rec_902753,Human_Splice_Rec_902795,Human_Splice_Rec_902839,Human_Splice_Rec_902881,Human_Splice_Rec_902927 74640 RMVar_ID_74640 Human_SNP_ID_333056234 m1A Human chr7 - 101816095 101816095 101816095 CCCGGGCGCGAGGCCGAGCGCGGAGGAGCCTGACCTGCAGCTGCTGTAAATCAAAGCGCTTCCAA CCCGGGCGCGAGGCCGAGCGCGGAGGAGCCTGGCCTGCAGCTGCTGTAAATCAAAGCGCTTCCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101816069..101816512 26863196 MeRIP-seq:(Medium) rs1378944324 Functional Loss SNV dbSNP153 33..33 33 - - - 74641 RMVar_ID_74641 Human_SNP_ID_333056700 m1A Human chr7 - 101817203 101817203 101817203 CGGCTCGGACCGGCGGCGGGGAGGCAGCGTACACTGCCCGGGCACCCGGGGGAACAGCTTGGGGC CGGCTCGGACCGGCGGCGGGGAGGCAGCGTACGCTGCCCGGGCACCCGGGGGAACAGCTTGGGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101817153..101817363 26863196 MeRIP-seq:(Medium) rs899781568 Functional Loss SNV dbSNP153 33..33 33 - - - 74642 RMVar_ID_74642 Human_SNP_ID_333056871 m1A Human chr7 - 101817671 101817671 101817671 CAACCTCGGGACTTCTGGCCCACACGCCGCTCACCTTCAACCTGGCTCCGGCTACGCACAACATC CAACCTCGGGACTTCTGGCCCACACGCCGCTCTCCTTCAACCTGGCTCCGGCTACGCACAACATC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:101817662..101817769 26863196 MeRIP-seq:(Medium) rs983749883 Functional Loss SNV dbSNP153 33..33 33 - - - 74643 RMVar_ID_74643 Human_SNP_ID_333056876 m1A Human chr7 - 101817682 101817682 101817682 CTCCGCGCCTGCAACCTCGGGACTTCTGGCCCACACGCCGCTCACCTTCAACCTGGCTCCGGCTA CTCCGCGCCTGCAACCTCGGGACTTCTGGCCCCCACGCCGCTCACCTTCAACCTGGCTCCGGCTA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101817673..101817778 26863196 MeRIP-seq:(Medium) rs1341417729 Functional Loss SNV dbSNP153 33..33 33 - - - 74644 RMVar_ID_74644 Human_SNP_ID_333060047 m1A Human chr7 - 101828788 101828788 101828788 CCTCCTCTCCCAGCCCTCACTTCCCCAAATCCAAGCAAATGCTTCTGCAGCCAGACAGTGATGTC CCTCCTCTCCCAGCCCTCACTTCCCCAAATCCCAGCAAATGCTTCTGCAGCCAGACAGTGATGTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:101828781..101828930;chr7:101828778..101829202;chr7:101828780..101828905 26863196 MeRIP-seq:(Medium) rs1359048813 Functional Loss SNV dbSNP153 33..33 33 - - - 74645 RMVar_ID_74645 Human_SNP_ID_333070315 m1A Human chr7 - 101868688 101868688 101868688 CACTTCATCATCCATTCTGAGCTTTGCGGCTGATGGTATTTAACTTAAACCAACTCCTGCTTCAG CACTTCATCATCCATTCTGAGCTTTGCGGCTGGTGGTATTTAACTTAAACCAACTCCTGCTTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101868681..101869243 26863196 MeRIP-seq:(Medium) rs969019356 Functional Loss SNV dbSNP153 33..33 33 - - - 74646 RMVar_ID_74646 Human_SNP_ID_333070381 m1A Human chr7 + 101868972 101868972 101868972 CTGGGCGAGAACAGGAGAGGAGAGGCCCCTGGATGCCAGCAGAGCTGTAGGCATGATCTGGGCCA CTGGGCGAGAACAGGAGAGGAGAGGCCCCTGGGTGCCAGCAGAGCTGTAGGCATGATCTGGGCCA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101868969..101869162 26863196 MeRIP-seq:(Medium) rs760051806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3862567,Human_RBP_ID_8149593,Human_RBP_ID_8652897,Human_RBP_ID_18504104 74647 RMVar_ID_74647 Human_SNP_ID_333070553 m1A Human chr7 - 101869593 101869593 101869593 CCTGCTGGCCGCCTGACCTTGGCTGACCTTCTAACGTGCTGGTTTCCCTCCCCCGCCCCACCAGC CCTGCTGGCCGCCTGACCTTGGCTGACCTTCTCACGTGCTGGTTTCCCTCCCCCGCCCCACCAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101869585..101869707 26863196 MeRIP-seq:(Medium) rs972136190 Functional Loss SNV dbSNP153 33..33 33 - - - 74648 RMVar_ID_74648 Human_SNP_ID_333079659 m1A Human chr7 + 101906282 101906282 101906282 ACCAACCCTGTGCCCAGACTAGGGGAGCTGCCACGCAGCCACTCACTGAGCTGGGCACACAGGTT ACCAACCCTGTGCCCAGACTAGGGGAGCTGCCGCGCAGCCACTCACTGAGCTGGGCACACAGGTT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:101906272..101906447 26863196 MeRIP-seq:(Medium) rs1243349358 Functional Loss SNV dbSNP153 33..33 33 - - - 74649 RMVar_ID_74649 Human_SNP_ID_333087154 m1A Human chr7 + 101936404 101936404 101936404 AAGAGAGGCACGAACGTCATTTCCAGAGCGAGATGAAGGTCACAGAGTTTGGGAGGAGATGGGAT AAGAGAGGCACGAACGTCATTTCCAGAGCGAGGTGAAGGTCACAGAGTTTGGGAGGAGATGGGAT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:101936398..101936504 26863196 MeRIP-seq:(Medium) rs963153717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_320822,RMVar_hsa_circ_352082,RMVar_hsa_circ_307725,RMVar_hsa_circ_296973,RMVar_hsa_circ_304656,RMVar_hsa_circ_247261 74650 RMVar_ID_74650 Human_SNP_ID_333089537 m1A Human chr7 - 101945966 101945966 101945966 CCTGACCACAGAACCACTCATTGGAAGTGCATAGAACTCATTCTTTAAATAAGCAAATGCCTTGT CCTGACCACAGAACCACTCATTGGAAGTGCATTGAACTCATTCTTTAAATAAGCAAATGCCTTGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:101945958..101946205 26863196 MeRIP-seq:(Medium) rs1251543035 Functional Loss SNV dbSNP153 33..33 33 - - - 74651 RMVar_ID_74651 Human_SNP_ID_333115254 m1A Human chr7 - 102047204 102047204 102047204 ATCACTTAACAGAGCGCCAAGCACTGTGCCACATGGGGATACAGATCTTGCTAAACTGTTAAGCT ATCACTTAACAGAGCGCCAAGCACTGTGCCACGTGGGGATACAGATCTTGCTAAACTGTTAAGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:102047198..102047491 26863196 MeRIP-seq:(Medium) rs780602433 Functional Loss SNV dbSNP153 33..33 33 - - - 74652 RMVar_ID_74652 Human_SNP_ID_333122192 m1A Human chr7 - 102074069 102074069 102074069 CTTCCTGTAAGCCTCAGCCACAGAATGATTGCATCTGAGCAATAATCAGACTTCAAAACACAGGG CTTCCTGTAAGCCTCAGCCACAGAATGATTGCGTCTGAGCAATAATCAGACTTCAAAACACAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:102074058..102074174 26863196 MeRIP-seq:(Medium) rs1480174304 Functional Loss SNV dbSNP153 33..33 33 - - - 74653 RMVar_ID_74653 Human_SNP_ID_333122930 m1A Human chr7 + 102077140 102077140 102077140 AAGCAAAGCCCACTGGGCAATGAGAGTATAGAATAAGGTGAATCAAGCAGGACAGAGGCAGCTGC AAGCAAAGCCCACTGGGCAATGAGAGTATAGAGTAAGGTGAATCAAGCAGGACAGAGGCAGCTGC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:102077128..102077234 26863196 MeRIP-seq:(Medium) rs1163910845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15951553 RMVar_hsa_circ_36611,RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_352082,RMVar_hsa_circ_296973,RMVar_hsa_circ_304656,RMVar_hsa_circ_112469,RMVar_hsa_circ_247261,RMVar_hsa_circ_351005,RMVar_hsa_circ_363183,RMVar_hsa_circ_324040,RMVar_hsa_circ_357667,RMVar_hsa_circ_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_247262,RMVar_hsa_circ_26032,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264 74654 RMVar_ID_74654 Human_SNP_ID_333137288 m1A Human chr7 + 102132096 102132096 102132096 AAAAACTTTTTTTTAAGCATGATGCCAAAAGTAGAAATCACAAAGGGAAGAAATTCAGAGCTTTG AAAAACTTTTTTTTAAGCATGATGCCAAAAGTGGAAATCACAAAGGGAAGAAATTCAGAGCTTTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102132093..102132271 26863196 MeRIP-seq:(Medium) rs1023950573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_296973,RMVar_hsa_circ_112469,RMVar_hsa_circ_247261,RMVar_hsa_circ_363183,RMVar_hsa_circ_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_247268,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269 74655 RMVar_ID_74655 Human_SNP_ID_333143813 m1A Human chr7 + 102156948 102156948 102156948 CAAACCTGGAAACTAGGACTAGGGACAGTGCCACTTCCTGAGACAGAGCTGCTGAGAGGGTCTGG CAAACCTGGAAACTAGGACTAGGGACAGTGCCGCTTCCTGAGACAGAGCTGCTGAGAGGGTCTGG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:102156944..102157106 26863196 MeRIP-seq:(Medium) rs1307296444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15952567 RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_296973,RMVar_hsa_circ_112469,RMVar_hsa_circ_247261,RMVar_hsa_circ_363183,RMVar_hsa_circ_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_247268,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269 74656 RMVar_ID_74656 Human_SNP_ID_333143821 m1A Human chr7 + 102156983 102156983 102156983 TCCTGAGACAGAGCTGCTGAGAGGGTCTGGGAAGGGTGGATGGGGTGGAAGTAGGAGATGAGGTT TCCTGAGACAGAGCTGCTGAGAGGGTCTGGGAGGGGTGGATGGGGTGGAAGTAGGAGATGAGGTT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102156978..102157153 26863196 MeRIP-seq:(Medium) rs1389905973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3033033 RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_296973,RMVar_hsa_circ_112469,RMVar_hsa_circ_247261,RMVar_hsa_circ_363183,RMVar_hsa_circ_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_247268,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269 74657 RMVar_ID_74657 Human_SNP_ID_333145484 m1A Human chr7 + 102163441 102163441 102163441 TCTCTTGGGCCCGAGAGTTCAAAACCAACACCAGAGATGCGGGTCAGAGAGTGGGCTGGTAGGAC TCTCTTGGGCCCGAGAGTTCAAAACCAACACCGGAGATGCGGGTCAGAGAGTGGGCTGGTAGGAC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:102163433..102163782 26863196 MeRIP-seq:(Medium) rs1008109781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15952643 RMVar_hsa_circ_304804,RMVar_hsa_circ_296973,RMVar_hsa_circ_112469,RMVar_hsa_circ_247261,RMVar_hsa_circ_363183,RMVar_hsa_circ_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_247268,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_247271,RMVar_hsa_circ_274211,RMVar_hsa_circ_298295,RMVar_hsa_circ_318945,RMVar_hsa_circ_104972,RMVar_hsa_circ_247270 74658 RMVar_ID_74658 Human_SNP_ID_333154514 m1A Human chr7 - 102196974 102196974 102196974 ATGCCATTGACATCTGGGCTTTGTTGTAATGGACTTTGGGAAGATATGGAGTTTGTGCTGTATGG ATGCCATTGACATCTGGGCTTTGTTGTAATGGTCTTTGGGAAGATATGGAGTTTGTGCTGTATGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:102196925..102197140 26863196 MeRIP-seq:(Medium) rs1554518536 Functional Loss SNV dbSNP153 33..33 33 - - - 74659 RMVar_ID_74659 Human_SNP_ID_333155794 m1A Human chr7 + 102201509 102201509 102201509 CCTTAAAGCAGGCACCACTGTCCCAGAGTGACATCACCATCCTCACCCCCAAGCTTCTGTCCACC CCTTAAAGCAGGCACCACTGTCCCAGAGTGACGTCACCATCCTCACCCCCAAGCTTCTGTCCACC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:102201458..102201959 26863196 MeRIP-seq:(Medium) rs1554519711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86495,Human_RBP_ID_18872886 Human_miRNA_ID_1956807,Human_miRNA_ID_2466313,Human_miRNA_ID_2996228 RMVar_hsa_circ_112469,RMVar_hsa_circ_247268,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_68218,RMVar_hsa_circ_247271,RMVar_hsa_circ_104972,RMVar_hsa_circ_339616,RMVar_hsa_circ_31070,RMVar_hsa_circ_65158,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_367018,RMVar_hsa_circ_378451,RMVar_hsa_circ_247280,RMVar_hsa_circ_329143,RMVar_hsa_circ_65716,RMVar_hsa_circ_247282,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_247283,RMVar_hsa_circ_43829,RMVar_hsa_circ_264945 74660 RMVar_ID_74660 Human_SNP_ID_333155814 m1A Human chr7 - 102201558 102201558 102201558 TCAGGGAGATGGCGAGAGGTGGGTAGCTGGACACGGTGGGCATGGGCGAGGTGGACAGAAGCTTG TCAGGGAGATGGCGAGAGGTGGGTAGCTGGACGCGGTGGGCATGGGCGAGGTGGACAGAAGCTTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102201529..102201633 26863196 MeRIP-seq:(Medium) rs1339830792 Functional Loss SNV dbSNP153 33..33 33 - - - 74661 RMVar_ID_74661 Human_SNP_ID_333155931 m1A Human chr7 + 102201822 102201822 102201822 GAGAAGAAATGCCGCCTCCTCCGAGGAGGCCAAGGCCGAAGAAACGGGCGGCGGGAAAGAGAAGG GAGAAGAAATGCCGCCTCCTCCGAGGAGGCCACGGCCGAAGAAACGGGCGGCGGGAAAGAGAAGG A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:102201607..102201954 26863196 MeRIP-seq:(Medium) rs1320547987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86497,Human_RBP_ID_217423,Human_RBP_ID_953321,Human_RBP_ID_5533662,Human_RBP_ID_19020030,Human_RBP_ID_26356891 Human_miRNA_ID_2217553 RMVar_hsa_circ_112469,RMVar_hsa_circ_247268,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_68218,RMVar_hsa_circ_247271,RMVar_hsa_circ_104972,RMVar_hsa_circ_339616,RMVar_hsa_circ_31070,RMVar_hsa_circ_65158,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_367018,RMVar_hsa_circ_378451,RMVar_hsa_circ_247280,RMVar_hsa_circ_329143,RMVar_hsa_circ_65716,RMVar_hsa_circ_247282,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_247283,RMVar_hsa_circ_43829,RMVar_hsa_circ_264945 74662 RMVar_ID_74662 Human_SNP_ID_333155969 m1A Human chr7 + 102201882 102201882 102201882 GAAGGGCAGCGGTGGCAGCGGAGGTGGCAGCCAGCCTCGGGCCGAGCGCAGTCAGCTCCAGGGAC GAAGGGCAGCGGTGGCAGCGGAGGTGGCAGCCTGCCTCGGGCCGAGCGCAGTCAGCTCCAGGGAC A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102201622..102202127 26863196 MeRIP-seq:(Medium) rs782294140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_217423,Human_RBP_ID_5533663,Human_RBP_ID_19020030,Human_RBP_ID_22483061 Human_miRNA_ID_2331308,Human_miRNA_ID_2713980,Human_miRNA_ID_2964390,Human_miRNA_ID_3049958 RMVar_hsa_circ_112469,RMVar_hsa_circ_247268,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_68218,RMVar_hsa_circ_247271,RMVar_hsa_circ_104972,RMVar_hsa_circ_339616,RMVar_hsa_circ_31070,RMVar_hsa_circ_65158,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_367018,RMVar_hsa_circ_378451,RMVar_hsa_circ_247280,RMVar_hsa_circ_329143,RMVar_hsa_circ_65716,RMVar_hsa_circ_247282,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_247283,RMVar_hsa_circ_43829,RMVar_hsa_circ_264945 74663 RMVar_ID_74663 Human_SNP_ID_333156049 m1A Human chr7 + 102202064 102202064 102202064 CATCCTCCCCGATCGTGCCCATGTCCAAGCCCACCAAGCCCTCGGTCCCCCCGCTGACCCCCGAG CATCCTCCCCGATCGTGCCCATGTCCAAGCCCCCCAAGCCCTCGGTCCCCCCGCTGACCCCCGAG A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr7:102202013..102202161;chr7:102201939..102202125 26863196 MeRIP-seq:(Medium) rs917985604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86498,Human_RBP_ID_17427054 Human_miRNA_ID_2873120,Human_miRNA_ID_2981083 RMVar_hsa_circ_112469,RMVar_hsa_circ_247268,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_68218,RMVar_hsa_circ_247271,RMVar_hsa_circ_104972,RMVar_hsa_circ_339616,RMVar_hsa_circ_31070,RMVar_hsa_circ_65158,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_367018,RMVar_hsa_circ_378451,RMVar_hsa_circ_247280,RMVar_hsa_circ_329143,RMVar_hsa_circ_65716,RMVar_hsa_circ_247282,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_247283,RMVar_hsa_circ_43829,RMVar_hsa_circ_264945 74664 RMVar_ID_74664 Human_SNP_ID_333156050 m1A Human chr7 + 102202064 102202064 102202064 CATCCTCCCCGATCGTGCCCATGTCCAAGCCCACCAAGCCCTCGGTCCCCCCGCTGACCCCCGAG CATCCTCCCCGATCGTGCCCATGTCCAAGCCCGCCAAGCCCTCGGTCCCCCCGCTGACCCCCGAG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr7:102202013..102202161;chr7:102201939..102202125 26863196 MeRIP-seq:(Medium) rs917985604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86498,Human_RBP_ID_17427054 Human_miRNA_ID_2873120,Human_miRNA_ID_2981083 RMVar_hsa_circ_112469,RMVar_hsa_circ_247268,RMVar_hsa_circ_247264,RMVar_hsa_circ_84013,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_68218,RMVar_hsa_circ_247271,RMVar_hsa_circ_104972,RMVar_hsa_circ_339616,RMVar_hsa_circ_31070,RMVar_hsa_circ_65158,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_367018,RMVar_hsa_circ_378451,RMVar_hsa_circ_247280,RMVar_hsa_circ_329143,RMVar_hsa_circ_65716,RMVar_hsa_circ_247282,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_247283,RMVar_hsa_circ_43829,RMVar_hsa_circ_264945 74665 RMVar_ID_74665 Human_SNP_ID_333168891 m1A Human chr7 + 102248500 102248500 102248500 AGGCGGGCGCCAGCGACTCACCCTCGGCCCGCAGCGGCCGGGCGGCGCCCAGCTCGGAGGGCGAC AGGCGGGCGCCAGCGACTCACCCTCGGCCCGCGGCGGCCGGGCGGCGCCCAGCTCGGAGGGCGAC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr7:102248451..102248653;chr7:102248457..102248748 26863196 MeRIP-seq:(Medium) rs1268563772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9311414 Human_Splice_Rec_902652,Human_Splice_Rec_902694,Human_Splice_Rec_902926,Human_Splice_Rec_903014,Human_Splice_Rec_903060,Human_Splice_Rec_903104,Human_Splice_Rec_903146,Human_Splice_Rec_903188 RMVar_hsa_circ_85687,RMVar_hsa_circ_247267,RMVar_hsa_circ_267024,RMVar_hsa_circ_264945,RMVar_hsa_circ_266127,RMVar_hsa_circ_87521,RMVar_hsa_circ_247291 74666 RMVar_ID_74666 Human_SNP_ID_333169033 m1A Human chr7 + 102248793 102248793 102248793 GCGCCCGCGGCCCCCGAGGACGCCGCTACCTCAGCCGCCGCCGCGCCGGGGGAGGGCCCCGCGGC GCGCCCGCGGCCCCCGAGGACGCCGCTACCTCGGCCGCCGCCGCGCCGGGGGAGGGCCCCGCGGC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:102248751..102248925 26863196 MeRIP-seq:(Medium) rs1255258411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85687,RMVar_hsa_circ_247267,RMVar_hsa_circ_267024,RMVar_hsa_circ_264945,RMVar_hsa_circ_266127,RMVar_hsa_circ_87521,RMVar_hsa_circ_247291 74667 RMVar_ID_74667 Human_SNP_ID_333169077 m1A Human chr7 - 102248833 102248833 102248833 GCTGCTGCTGCTGTTGCTGGGCGGCGGCGCGGAGCTCGGGGCCGCGGGGCCCTCCCCCGGCGCGG GCTGCTGCTGCTGTTGCTGGGCGGCGGCGCGGGGCTCGGGGCCGCGGGGCCCTCCCCCGGCGCGG T C RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102248793..102249070 26863196 MeRIP-seq:(Medium) rs1408297967 Functional Loss SNV dbSNP153 33..33 33 - - - 74668 RMVar_ID_74668 Human_SNP_ID_333179699 m1A Human chr7 + 102286985 102286985 102286985 CAGGAGCCTTCGAGGCGGTGAACGAGGGAGGGAGCCCAGTCCGCCGCGGGCCATGAGCCACCGGG CAGGAGCCTTCGAGGCGGTGAACGAGGGAGGGTGCCCAGTCCGCCGCGGGCCATGAGCCACCGGG A T SH2B2 Ensembl:ENSG00000160999 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102286872..102287123 26863196 MeRIP-seq:(Medium) rs1447570459 Functional Loss SNV dbSNP153 33..33 33 - - - 74669 RMVar_ID_74669 Human_SNP_ID_333191633 m1A Human chr7 + 102329588 102329588 102329588 CAGGAAGACGAGGACCGCAGGGTAGGTTTGGCAATCCAGCTGGGGAAGAAAGAGAAGAAAGGGCT CAGGAAGACGAGGACCGCAGGGTAGGTTTGGCGATCCAGCTGGGGAAGAAAGAGAAGAAAGGGCT A G RF00017-4498 RNACentral:URS0000923951 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102329460..102329638 26863196 MeRIP-seq:(Medium) rs2906698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7668048 74670 RMVar_ID_74670 Human_SNP_ID_333207911 m1A Human chr7 + 102396455 102396455 102396455 AGCCGCCTCCTCGGTGCGACCACCGAGGCCCAAGAAAGAGCCGCAGACGCTCGTCATCCCCAAGA AGCCGCCTCCTCGGTGCGACCACCGAGGCCCAGGAAAGAGCCGCAGACGCTCGTCATCCCCAAGA A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102396406..102396602 26863196 MeRIP-seq:(Medium) rs1554570340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_903419,Human_Splice_Rec_903451 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_303660,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306 74671 RMVar_ID_74671 Human_SNP_ID_333208898 m1A Human chr7 + 102399614 102399614 102399614 CGTGTACAGACATCTGCGCCGGAGAGAATATCAGCGACAGGACTACATGGATGCCATGGCTGAGA CGTGTACAGACATCTGCGCCGGAGAGAATATCCGCGACAGGACTACATGGATGCCATGGCTGAGA A C PRKRIP1 Ensembl:ENSG00000128563 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102397656..102404364 26863196 MeRIP-seq:(Medium) rs782266026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954825,Human_RBP_ID_1679676,Human_RBP_ID_2031931,Human_RBP_ID_3033292,Human_RBP_ID_3824214,Human_RBP_ID_15953772,Human_RBP_ID_18540046,Human_RBP_ID_18872929,Human_RBP_ID_27829654 Human_Splice_Rec_903376,Human_Splice_Rec_903377,Human_Splice_Rec_903388,Human_Splice_Rec_903389,Human_Splice_Rec_903404,Human_Splice_Rec_903405,Human_Splice_Rec_903422,Human_Splice_Rec_903423,Human_Splice_Rec_903436,Human_Splice_Rec_903437,Human_Splice_Rec_903444,Human_Splice_Rec_903445,Human_Splice_Rec_903454,Human_Splice_Rec_903455 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_303660,RMVar_hsa_circ_350579,RMVar_hsa_circ_247307,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_270966,RMVar_hsa_circ_247308,RMVar_hsa_circ_247310,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 74672 RMVar_ID_74672 Human_SNP_ID_333208899 m1A Human chr7 + 102399614 102399614 102399614 CGTGTACAGACATCTGCGCCGGAGAGAATATCAGCGACAGGACTACATGGATGCCATGGCTGAGA CGTGTACAGACATCTGCGCCGGAGAGAATATCTGCGACAGGACTACATGGATGCCATGGCTGAGA A T PRKRIP1 Ensembl:ENSG00000128563 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102397656..102404364 26863196 MeRIP-seq:(Medium) rs782266026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954825,Human_RBP_ID_1679676,Human_RBP_ID_2031931,Human_RBP_ID_3033292,Human_RBP_ID_3824214,Human_RBP_ID_15953772,Human_RBP_ID_18540046,Human_RBP_ID_18872929,Human_RBP_ID_27829654 Human_Splice_Rec_903376,Human_Splice_Rec_903377,Human_Splice_Rec_903388,Human_Splice_Rec_903389,Human_Splice_Rec_903404,Human_Splice_Rec_903405,Human_Splice_Rec_903422,Human_Splice_Rec_903423,Human_Splice_Rec_903436,Human_Splice_Rec_903437,Human_Splice_Rec_903444,Human_Splice_Rec_903445,Human_Splice_Rec_903454,Human_Splice_Rec_903455 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_303660,RMVar_hsa_circ_350579,RMVar_hsa_circ_247307,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_270966,RMVar_hsa_circ_247308,RMVar_hsa_circ_247310,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 74673 RMVar_ID_74673 Human_SNP_ID_333215830 m1A Human chr7 + 102425938 102425938 102425938 GGGTCTAAACAGAACAGGCTGAGAGAGGCGGGACTGGGTCAAGTGGGTGGAGCTCCTCCTTGCAT GGGTCTAAACAGAACAGGCTGAGAGAGGCGGGGCTGGGTCAAGTGGGTGGAGCTCCTCCTTGCAT A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:102425704..102426077;chr7:102425393..102426621 26863196 MeRIP-seq:(Medium) rs944920343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7668209,Human_RBP_ID_15954456,Human_RBP_ID_18087703 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_108617,RMVar_hsa_circ_247315 74674 RMVar_ID_74674 Human_SNP_ID_333215834 m1A Human chr7 - 102425953 102425953 102425953 CCGACAGTTGCAGTCATGCAAGGAGGAGCTCCACCCACTTGACCCAGTCCCGCCTCTCTCAGCCT CCGACAGTTGCAGTCATGCAAGGAGGAGCTCCCCCCACTTGACCCAGTCCCGCCTCTCTCAGCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102425671..102426292 26863196 MeRIP-seq:(Medium) rs1554574397 Functional Loss SNV dbSNP153 33..33 33 - - - 74675 RMVar_ID_74675 Human_SNP_ID_333218015 m1A Human chr7 + 102433615 102433615 102433615 GGCCGGGCCACTGGGCCACAGGCCACGCGGCCACGCAGTCCGAGCGGGAGCCGAGCCGGGCGGGG GGCCGGGCCACTGGGCCACAGGCCACGCGGCCGCGCAGTCCGAGCGGGAGCCGAGCCGGGCGGGG A G ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:102433564..102433730;chr7:102433540..102433731 26863196 MeRIP-seq:(Medium) rs1026009413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4919083 Human_Splice_Rec_903499,Human_Splice_Rec_903503,Human_Splice_Rec_903509,Human_Splice_Rec_903513,Human_Splice_Rec_903519,Human_Splice_Rec_903525,Human_Splice_Rec_903529 74676 RMVar_ID_74676 Human_SNP_ID_333218017 m1A Human chr7 + 102433619 102433619 102433619 GGGCCACTGGGCCACAGGCCACGCGGCCACGCAGTCCGAGCGGGAGCCGAGCCGGGCGGGGCGAG GGGCCACTGGGCCACAGGCCACGCGGCCACGCGGTCCGAGCGGGAGCCGAGCCGGGCGGGGCGAG A G ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102433572..102433796 26863196 MeRIP-seq:(Medium) rs950599585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4919083 Human_Splice_Rec_903499,Human_Splice_Rec_903503,Human_Splice_Rec_903509,Human_Splice_Rec_903513,Human_Splice_Rec_903519,Human_Splice_Rec_903525,Human_Splice_Rec_903529 74677 RMVar_ID_74677 Human_SNP_ID_333221857 m1A Human chr7 + 102447060 102447053 102447060 TGAGCGCAGCCTGCAGGTCTTGTGAGGGGCCGAGGGCCGGGGCTGGGAGCGGCCCTGTGCCCGGG TGAGCGCAGCCTGCAGGTCTTGTGAG_______GGGCCGGGGCTGGGAGCGGCCCTGTGCCCGGG GGGGCCGA G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:102447012..102447113 32194978 MeRIP-seq:(Medium) rs1324267629 Functional Loss DEL dbSNP153 27..33 33 - - - 74678 RMVar_ID_74678 Human_SNP_ID_333222013 m1A Human chr7 + 102447507 102447507 102447507 GTGGACTTCATGGGTGCTGAGTGGCCCGTGTGACAGTGATGACACGAAGGCTTCGGCGTTTGAGT GTGGACTTCATGGGTGCTGAGTGGCCCGTGTGGCAGTGATGACACGAAGGCTTCGGCGTTTGAGT A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102447456..102447561;chr7:102447456..102447550 26863196 MeRIP-seq:(Medium) rs1249492975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24181049 74679 RMVar_ID_74679 Human_SNP_ID_333222790 m1A Human chr7 - 102450349 102450349 102450349 AGGAGAAGGCCCAGCAGGGCCCCTCCCAAAAGACTCAGGCCAGAGTAAGGGCCTGCTGCCTCTCC AGGAGAAGGCCCAGCAGGGCCCCTCCCAAAAGCCTCAGGCCAGAGTAAGGGCCTGCTGCCTCTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:102450298..102450548 32194978 MeRIP-seq:(Medium) rs1487056276 Functional Loss SNV dbSNP153 33..33 33 - - - 74680 RMVar_ID_74680 Human_SNP_ID_333226996 m1A Human chr7 - 102465076 102465059 102465076 TTAGCAGCCGCGCCGAGAGGGGGCCCATGGCGAGGAGGCGCAGCCCGCGCTGACCCAGTCGGCCA TTAGCAGCCGCGCCGAGAGGGGGCCCATGGCG_________________CTGACCCAGTCGGCCA GCGCGGGCTGCGCCTCCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:102465028..102465128 32194978 MeRIP-seq:(Medium) rs1167357978 Functional Loss DEL dbSNP153 33..49 33 - - - 74681 RMVar_ID_74681 Human_SNP_ID_333227012 m1A Human chr7 - 102465082 102465082 102465082 GCTGCATTAGCAGCCGCGCCGAGAGGGGGCCCATGGCGAGGAGGCGCAGCCCGCGCTGACCCAGT GCTGCATTAGCAGCCGCGCCGAGAGGGGGCCCGTGGCGAGGAGGCGCAGCCCGCGCTGACCCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102465032..102465132 26863196 MeRIP-seq:(Medium) rs1433067838 Functional Loss SNV dbSNP153 33..33 33 - - - 74682 RMVar_ID_74682 Human_SNP_ID_333231241 m1A Human chr7 - 102473596 102473596 102473596 CGGCCTGTGAGCCCCGTTCCTACCTGTGCCTGACCCTCCGCTCCAGGTACCACACCGAGGAGAGC CGGCCTGTGAGCCCCGTTCCTACCTGTGCCTGCCCCTCCGCTCCAGGTACCACACCGAGGAGAGC T G POLR2J Ensembl:ENSG00000005075 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:102473545..102473630;chr7:102473545..102473628 26863196 MeRIP-seq:(Medium) rs1290851519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671936,Human_RBP_ID_957211,Human_RBP_ID_1329438,Human_RBP_ID_5478912,Human_RBP_ID_9337939,Human_RBP_ID_9403764,Human_RBP_ID_17665108,Human_RBP_ID_18196038,Human_RBP_ID_22464197,Human_RBP_ID_26830670,Human_RBP_ID_27527590 Human_Splice_Rec_903652 RMVar_hsa_circ_78167,RMVar_hsa_circ_247336 74683 RMVar_ID_74683 Human_SNP_ID_333231247 m1A Human chr7 + 102473602 102473602 102473602 CTCGGTGTGGTACCTGGAGCGGAGGGTCAGGCACAGGTAGGAACGGGGCTCACAGGCCGAGCAGA CTCGGTGTGGTACCTGGAGCGGAGGGTCAGGCGCAGGTAGGAACGGGGCTCACAGGCCGAGCAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:102473504..102473951 32194978 MeRIP-seq:(Medium) rs780858399 Functional Loss SNV dbSNP153 33..33 33 - - - 74684 RMVar_ID_74684 Human_SNP_ID_333232966 m1A Human chr7 - 102478879 102478879 102478879 GGTGGCGGCGGCGGCGGACCCTTGGGGTCTGGACGCAACGGCGGCGGGAGCATGAACGCCCCTCC GGTGGCGGCGGCGGCGGACCCTTGGGGTCTGGGCGCAACGGCGGCGGGAGCATGAACGCCCCTCC T C POLR2J Ensembl:ENSG00000005075 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:102478767..102478925 26863196 MeRIP-seq:(Medium) rs1329363201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955954,Human_RBP_ID_5327982,Human_RBP_ID_18426548,Human_RBP_ID_22463259,Human_RBP_ID_27103322 Human_Splice_Rec_903647 74685 RMVar_ID_74685 Human_SNP_ID_333232980 m1A Human chr7 + 102478890 102478890 102478890 CATGCTCCCGCCGCCGTTGCGTCCAGACCCCAAGGGTCCGCCGCCGCCGCCACCAGAGCCCTAAT CATGCTCCCGCCGCCGTTGCGTCCAGACCCCAGGGGTCCGCCGCCGCCGCCACCAGAGCCCTAAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:102478828..102478925;chr7:102478826..102478925;chr7:102478817..102478925 26863196 MeRIP-seq:(Medium) rs1483288405 Functional Loss SNV dbSNP153 33..33 33 - - - 74686 RMVar_ID_74686 Human_SNP_ID_333241608 m1A Human chr7 - 102531288 102531274 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGA______________GAGAGAGAGAGATGAAAGA CTCCCCCCCCCCCTT C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1420890995 Functional Loss DEL dbSNP153 33..46 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74687 RMVar_ID_74687 Human_SNP_ID_333241617 m1A Human chr7 - 102531288 102531276 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGA____________GAGAGAGAGAGAGATGAAAGA CCCCCCCCCCCTT C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1444619592 Functional Loss DEL dbSNP153 33..44 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74688 RMVar_ID_74688 Human_SNP_ID_333241645 m1A Human chr7 - 102531288 102531286 102531289 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAG___GGGGGGGGGGGAGAGAGAGAGAGATGAAAGA CTTT C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1276582975 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74689 RMVar_ID_74689 Human_SNP_ID_333241646 m1A Human chr7 - 102531288 102531286 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGA__GGGGGGGGGGGAGAGAGAGAGAGATGAAAGA CTT C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1322994565 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74690 RMVar_ID_74690 Human_SNP_ID_333241647 m1A Human chr7 - 102531288 102531286 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGA_AGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA CTT CT lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1322994565 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74691 RMVar_ID_74691 Human_SNP_ID_333241649 m1A Human chr7 - 102531288 102531288 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAGAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA T C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1286392688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 74692 RMVar_ID_74692 Human_SNP_ID_333243156 m1A Human chr7 - 102538297 102538294 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACT___TTTTTTTTTTTTTTTGAGACGGAGTCTCAC AAAT A POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1284942674 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 74693 RMVar_ID_74693 Human_SNP_ID_333243158 m1A Human chr7 - 102538297 102538296 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACT_TTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC AT A POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs201449870 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 74694 RMVar_ID_74694 Human_SNP_ID_333243161 m1A Human chr7 - 102538297 102538297 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC T A POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1063548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 74695 RMVar_ID_74695 Human_SNP_ID_333243162 m1A Human chr7 - 102538297 102538297 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACTGTTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC T C POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1063548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 74696 RMVar_ID_74696 Human_SNP_ID_333249335 m1A Human chr7 - 102567952 102567952 102567952 ACGGGGTGGGCTGGACACTGGCCCGTGTGCCCAGGCCTGGGACAGCCCTGGCCTGTTTCTTCGGA ACGGGGTGGGCTGGACACTGGCCCGTGTGCCCGGGCCTGGGACAGCCCTGGCCTGTTTCTTCGGA T C POLR2J3,AC093668.1,POLR2J3:2 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249,Ensembl:ENSG00000285437 Protein coding,Protein coding,Protein coding CDS,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200859434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28775,RMVar_hsa_circ_97247,RMVar_hsa_circ_247346,RMVar_hsa_circ_96796,RMVar_hsa_circ_120312,RMVar_hsa_circ_247349,RMVar_hsa_circ_116919,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354,RMVar_hsa_circ_119166,RMVar_hsa_circ_247356 74697 RMVar_ID_74697 Human_SNP_ID_333259644 m1A Human chr7 - 102630363 102630363 102630363 AAAGGGAGGGGGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGAAAGAGAAGGAAGG AAAGGGAGGGGGAGAGAGAGAGAGAGAGAGAGCGAGAGAGAGAGAGAGATGAAAGAGAAGGAAGG T G AC105052.1,AC105052.4 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102630281..102630398 26863196 MeRIP-seq:(Medium) rs1161098173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82174 RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74698 RMVar_ID_74698 Human_SNP_ID_333259645 m1A Human chr7 - 102630365 102630364 102630365 AGAAAGGGAGGGGGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGAAAGAGAAGGAA AGAAAGGGAGGGGGAGAGAGAGAGAGAGAGAG_GAGAGAGAGAGAGAGAGATGAAAGAGAAGGAA CT C AC105052.1,AC105052.4 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102630288..102630413 26863196 MeRIP-seq:(Medium) rs1562809223 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_82174 RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74699 RMVar_ID_74699 Human_SNP_ID_333259646 m1A Human chr7 - 102630365 102630365 102630365 AGAAAGGGAGGGGGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGATGAAAGAGAAGGAA AGAAAGGGAGGGGGAGAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGATGAAAGAGAAGGAA T C AC105052.1,AC105052.4 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102630288..102630413 26863196 MeRIP-seq:(Medium) rs867805393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82174 RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74700 RMVar_ID_74700 Human_SNP_ID_333261515 m1A Human chr7 - 102637217 102637217 102637217 CATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGGCCTCCATCTCTTGA CATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGATGGCCTCCATCTCTTGA T C AC105052.1,AC105052.4,AC105052.3,UPK3BL1 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168,Ensembl:ENSG00000267645,Ensembl:ENSG00000267368 Protein coding,lincRNA,Protein coding,Protein coding intron,intron,3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1140580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74701 RMVar_ID_74701 Human_SNP_ID_333261519 m1A Human chr7 - 102637231 102637231 102637231 CACCATGCCCAGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGG CACCATGCCCAGCTCATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGATGG T C AC105052.1,AC105052.4,AC105052.3,UPK3BL1 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168,Ensembl:ENSG00000267645,Ensembl:ENSG00000267368 Protein coding,lincRNA,Protein coding,Protein coding intron,intron,3'UTR,3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1140579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74702 RMVar_ID_74702 Human_SNP_ID_333261546 m1A Human chr7 + 102637342 102637342 102637342 TCGCTTGAACCCGTGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCAGCCTGGCGACAGAGTGA TCGCTTGAACCCGTGAGGCAGAGGTTGCAGTGGGCCAAGATCGCGCCAGCCTGGCGACAGAGTGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:102637251..102637406 26863410 MeRIP-seq:(Medium) rs1179924230 Functional Loss SNV dbSNP153 33..33 33 - - - 74703 RMVar_ID_74703 Human_SNP_ID_333261883 m1A Human chr7 - 102638638 102638638 102638638 CGGGGCCCTTGGGCATTAACCCCTCCCTCTCTAGTTCCTCCCCGCCCGCCCCTGCCCACCTTCCA CGGGGCCCTTGGGCATTAACCCCTCCCTCTCTCGTTCCTCCCCGCCCGCCCCTGCCCACCTTCCA T G AC105052.1,AC105052.4,AC105052.3,UPK3BL1 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168,Ensembl:ENSG00000267645,Ensembl:ENSG00000267368 Protein coding,lincRNA,Protein coding,Protein coding intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs865881421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 74704 RMVar_ID_74704 Human_SNP_ID_333357121 m1A Human chr7 - 103074967 103074967 103074967 GTGCGCCCCACGCGGAGACGCCGGGGCCCGCAACCCAGAGCCGAGCTTCCCGTCTCTTCCCCCGG GTGCGCCCCACGCGGAGACGCCGGGGCCCGCAGCCCAGAGCCGAGCTTCCCGTCTCTTCCCCCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:103074930..103075072 26863196 MeRIP-seq:(Medium) rs551367320 Functional Loss SNV dbSNP153 33..33 33 - - - 74705 RMVar_ID_74705 Human_SNP_ID_333357248 m1A Human chr7 - 103075201 103075201 103075201 GGAGGCTCGCGGGGGCCAGCGCGGAGGTCTCCAGCGCACGCGGGCCTAGCCGCCACAGCAAACGC GGAGGCTCGCGGGGGCCAGCGCGGAGGTCTCCGGCGCACGCGGGCCTAGCCGCCACAGCAAACGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:103074920..103075843;chr7:103074939..103075379 26863196 MeRIP-seq:(Medium) rs1412263370 Functional Loss SNV dbSNP153 33..33 33 - - - 74706 RMVar_ID_74706 Human_SNP_ID_333357274 m1A Human chr7 - 103075250 103075250 103075250 GGCCACCCATGCTGCCGCCGCGGCAGAGCCGCAGCGCCGGGCCAGGGCAGGAGGCTCGCGGGGGC GGCCACCCATGCTGCCGCCGCGGCAGAGCCGCCGCGCCGGGCCAGGGCAGGAGGCTCGCGGGGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:103075151..103075379 26863410 MeRIP-seq:(Medium) rs1469219356 Functional Loss SNV dbSNP153 33..33 33 - - - 74707 RMVar_ID_74707 Human_SNP_ID_333368284 m1A Human chr7 - 103120040 103120040 103120040 TCTTTAGCTCTCGTGCTTCACCATCGCAGTACATGGGTCCAAAGCGATTTCGTCGTTCCCCGTGC TCTTTAGCTCTCGTGCTTCACCATCGCAGTACGTGGGTCCAAAGCGATTTCGTCGTTCCCCGTGC T C NAPEPLD Ensembl:ENSG00000161048 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:103120003..103120139 26863196 MeRIP-seq:(Medium) rs775611160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276379,RMVar_hsa_circ_247418,RMVar_hsa_circ_247416,RMVar_hsa_circ_15275,RMVar_hsa_circ_247417,RMVar_hsa_circ_285336,RMVar_hsa_circ_369342 74708 RMVar_ID_74708 Human_SNP_ID_333368285 m1A Human chr7 - 103120040 103120040 103120040 TCTTTAGCTCTCGTGCTTCACCATCGCAGTACATGGGTCCAAAGCGATTTCGTCGTTCCCCGTGC TCTTTAGCTCTCGTGCTTCACCATCGCAGTACCTGGGTCCAAAGCGATTTCGTCGTTCCCCGTGC T G NAPEPLD Ensembl:ENSG00000161048 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:103120003..103120139 26863196 MeRIP-seq:(Medium) rs775611160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276379,RMVar_hsa_circ_247418,RMVar_hsa_circ_247416,RMVar_hsa_circ_15275,RMVar_hsa_circ_247417,RMVar_hsa_circ_285336,RMVar_hsa_circ_369342 74709 RMVar_ID_74709 Human_SNP_ID_333369004 m1A Human chr7 - 103123074 103123074 103123074 TGGGATGAGTACCGTGCAGGGTTCTTGAGCTCAGTCTAGGAGTAGGAAGCAGTCTCCATGTAGGT TGGGATGAGTACCGTGCAGGGTTCTTGAGCTCGGTCTAGGAGTAGGAAGCAGTCTCCATGTAGGT T C NAPEPLD Ensembl:ENSG00000161048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:103123025..103123090 26863196 MeRIP-seq:(Medium) rs1158414743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276379,RMVar_hsa_circ_247418,RMVar_hsa_circ_247416,RMVar_hsa_circ_247417,RMVar_hsa_circ_285336,RMVar_hsa_circ_369342 74710 RMVar_ID_74710 Human_SNP_ID_333408835 m1A Human chr7 - 103298524 103298513 103298525 TAGGAAGTGGAAGAGACAAAGCAAAACACATTACTAATCTGATATTAAATGTTGCTTTTAAAACC TAGGAAGTGGAAGAGACAAAGCAAAACACAT____________ATTAAATGTTGCTTTTAAAACC TATCAGATTAGTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:103298521..103298650 26863196 MeRIP-seq:(Medium) rs1327779399 Functional Loss DEL dbSNP153 32..43 33 - - - 74711 RMVar_ID_74711 Human_SNP_ID_333408837 m1A Human chr7 + 103298517 103298517 103298517 TAGATTTGGTTTTAAAAGCAACATTTAATATCAGATTAGTAATGTGTTTTGCTTTGTCTCTTCCA TAGATTTGGTTTTAAAAGCAACATTTAATATCTGATTAGTAATGTGTTTTGCTTTGTCTCTTCCA A T PMPCB Ensembl:ENSG00000105819 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:103298514..103298625 26863196 MeRIP-seq:(Medium) rs1428938700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22687218 RMVar_hsa_circ_1327 74712 RMVar_ID_74712 Human_SNP_ID_333415010 m1A Human chr7 - 103322025 103322025 103322025 GCTCGGTTAGCTAAGGAGAAAGAAGAGGAGGAAGTCAGACAGCAAGCATTGCTGGCAAAGAAGGA GCTCGGTTAGCTAAGGAGAAAGAAGAGGAGGATGTCAGACAGCAAGCATTGCTGGCAAAGAAGGA T A DNAJC2 Ensembl:ENSG00000105821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:103321976..103322109 26863196 MeRIP-seq:(Medium) rs1374647532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83487,Human_RBP_ID_844161,Human_RBP_ID_954837,Human_RBP_ID_1691030,Human_RBP_ID_3033805,Human_RBP_ID_4958765,Human_RBP_ID_9403774,Human_RBP_ID_18414218,Human_RBP_ID_24549002,Human_RBP_ID_26356926,Human_RBP_ID_27103390,Human_RBP_ID_27829667 Human_Splice_Rec_905408,Human_Splice_Rec_905409,Human_Splice_Rec_905440,Human_Splice_Rec_905441,Human_Splice_Rec_905466,Human_Splice_Rec_905467,Human_Splice_Rec_905498,Human_Splice_Rec_905499 RMVar_hsa_circ_9991,RMVar_hsa_circ_53638,RMVar_hsa_circ_247437,RMVar_hsa_circ_63283,RMVar_hsa_circ_286005,RMVar_hsa_circ_62743,RMVar_hsa_circ_59258,RMVar_hsa_circ_312367,RMVar_hsa_circ_44789,RMVar_hsa_circ_327812,RMVar_hsa_circ_335950,RMVar_hsa_circ_282373,RMVar_hsa_circ_247438 74713 RMVar_ID_74713 Human_SNP_ID_333415016 m1A Human chr7 - 103322041 103322041 103322041 AGCTGAATTAGAAGCTGCTCGGTTAGCTAAGGAGAAAGAAGAGGAGGAAGTCAGACAGCAAGCAT AGCTGAATTAGAAGCTGCTCGGTTAGCTAAGGGGAAAGAAGAGGAGGAAGTCAGACAGCAAGCAT T C DNAJC2 Ensembl:ENSG00000105821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:103321960..103322100 26863196 MeRIP-seq:(Medium) rs200342518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83487,Human_RBP_ID_844161,Human_RBP_ID_954837,Human_RBP_ID_1691030,Human_RBP_ID_3033806,Human_RBP_ID_9403774,Human_RBP_ID_18414218,Human_RBP_ID_24549002,Human_RBP_ID_26356926,Human_RBP_ID_27829667 Human_Splice_Rec_905408,Human_Splice_Rec_905440,Human_Splice_Rec_905466,Human_Splice_Rec_905498 RMVar_hsa_circ_9991,RMVar_hsa_circ_53638,RMVar_hsa_circ_247437,RMVar_hsa_circ_63283,RMVar_hsa_circ_286005,RMVar_hsa_circ_62743,RMVar_hsa_circ_59258,RMVar_hsa_circ_312367,RMVar_hsa_circ_44789,RMVar_hsa_circ_327812,RMVar_hsa_circ_335950,RMVar_hsa_circ_282373,RMVar_hsa_circ_247438 74714 RMVar_ID_74714 Human_SNP_ID_333415157 m1A Human chr7 - 103322560 103322560 103322560 GGAAGAAGAAAAAGCCAAGAAAGAAGCAGAAAAGAAAGCAAAAGCAGAAGCTAAACGGAAGGAGC GGAAGAAGAAAAAGCCAAGAAAGAAGCAGAAAGGAAAGCAAAAGCAGAAGCTAAACGGAAGGAGC T C DNAJC2 Ensembl:ENSG00000105821 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:103322470..103322721 26863196 MeRIP-seq:(Medium) rs369313610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954838,Human_RBP_ID_1690945,Human_RBP_ID_3033811,Human_RBP_ID_17664676,Human_RBP_ID_22832990,Human_RBP_ID_24549003,Human_RBP_ID_26356927,Human_RBP_ID_27830649 Human_Splice_Rec_905406,Human_Splice_Rec_905407,Human_Splice_Rec_905438,Human_Splice_Rec_905439,Human_Splice_Rec_905465,Human_Splice_Rec_905497,Human_Splice_Rec_905528 Human_miRNA_ID_2359517 RMVar_hsa_circ_9991,RMVar_hsa_circ_247437,RMVar_hsa_circ_63283,RMVar_hsa_circ_286005,RMVar_hsa_circ_59258,RMVar_hsa_circ_312367,RMVar_hsa_circ_44789,RMVar_hsa_circ_327812,RMVar_hsa_circ_335950,RMVar_hsa_circ_282373,RMVar_hsa_circ_247438 74715 RMVar_ID_74715 Human_SNP_ID_333415158 m1A Human chr7 - 103322562 103322562 103322562 AAGGAAGAAGAAAAAGCCAAGAAAGAAGCAGAAAAGAAAGCAAAAGCAGAAGCTAAACGGAAGGA AAGGAAGAAGAAAAAGCCAAGAAAGAAGCAGAGAAGAAAGCAAAAGCAGAAGCTAAACGGAAGGA T C DNAJC2 Ensembl:ENSG00000105821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:103322466..103322575 26863196 MeRIP-seq:(Medium) rs201299290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954838,Human_RBP_ID_1690945,Human_RBP_ID_3033811,Human_RBP_ID_5402349,Human_RBP_ID_17664676,Human_RBP_ID_22832990,Human_RBP_ID_24549003,Human_RBP_ID_26356927,Human_RBP_ID_27830649 Human_Splice_Rec_905406,Human_Splice_Rec_905407,Human_Splice_Rec_905438,Human_Splice_Rec_905439,Human_Splice_Rec_905465,Human_Splice_Rec_905497,Human_Splice_Rec_905528 Human_miRNA_ID_2359517 RMVar_hsa_circ_9991,RMVar_hsa_circ_247437,RMVar_hsa_circ_63283,RMVar_hsa_circ_286005,RMVar_hsa_circ_59258,RMVar_hsa_circ_312367,RMVar_hsa_circ_44789,RMVar_hsa_circ_327812,RMVar_hsa_circ_335950,RMVar_hsa_circ_282373,RMVar_hsa_circ_247438 74716 RMVar_ID_74716 Human_SNP_ID_333420509 m1A Human chr7 + 103344673 103344645 103344673 CCGGTGGGCGCAGCGGCTCACGTCCCGGGCGGAGGGCGCTTAGGGTCCCCTCCAGCTCTACCTCT CCGGT____________________________GGGCGCTTAGGGTCCCCTCCAGCTCTACCTCT TGGGCGCAGCGGCTCACGTCCCGGGCGGA T PSMC2 Ensembl:ENSG00000161057 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr7:103344576..103344807;chr7:103344576..103344750 26863196,26863410 MeRIP-seq:(Medium) rs939642166 Functional Loss DEL dbSNP153 6..33 33 - - - 74717 RMVar_ID_74717 Human_SNP_ID_333420526 m1A Human chr7 - 103344681 103344681 103344681 TCGGAGTGAGAGGTAGAGCTGGAGGGGACCCTAAGCGCCCTCCGCCCGGGACGTGAGCCGCTGCG TCGGAGTGAGAGGTAGAGCTGGAGGGGACCCTGAGCGCCCTCCGCCCGGGACGTGAGCCGCTGCG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:103344632..103344750 32194978 MeRIP-seq:(Medium) rs1477924545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86760,Human_RBP_ID_4919581,Human_RBP_ID_9311416,Human_RBP_ID_18472391,Human_RBP_ID_26356053,Human_RBP_ID_27830656 74718 RMVar_ID_74718 Human_SNP_ID_333420540 m1A Human chr7 - 103344703 103344703 103344703 TCTTAGAGCCAAGGCGCGAGGCTCGGAGTGAGAGGTAGAGCTGGAGGGGACCCTAAGCGCCCTCC TCTTAGAGCCAAGGCGCGAGGCTCGGAGTGAGTGGTAGAGCTGGAGGGGACCCTAAGCGCCCTCC T A DNAJC2 Ensembl:ENSG00000105821 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:103344551..103344825 26863196 MeRIP-seq:(Medium) rs1369990341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86760,Human_RBP_ID_4956587,Human_RBP_ID_8906661,Human_RBP_ID_9311417,Human_RBP_ID_9403780,Human_RBP_ID_19021383,Human_RBP_ID_26356053,Human_RBP_ID_27830656 74719 RMVar_ID_74719 Human_SNP_ID_333421339 m1A Human chr7 + 103347710 103347703 103347710 TCATTAAGGAGCGGAGGCTTTTGGAGCTGCTAAAATGCCGGATTACCTCGGTGCCGATCAGCGGA TCATTAAGGAGCGGAGGCTTTTGGAG_______AATGCCGGATTACCTCGGTGCCGATCAGCGGA GCTGCTAA G PSMC2 Ensembl:ENSG00000161057 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:103347651..103347826 26863196 MeRIP-seq:(Medium) rs756622974 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_85307,Human_RBP_ID_1049625,Human_RBP_ID_1219280,Human_RBP_ID_4919591,Human_RBP_ID_8653366,Human_RBP_ID_18087917,Human_RBP_ID_21557263,Human_RBP_ID_26356936,Human_RBP_ID_27830657 Human_Splice_Rec_905567,Human_Splice_Rec_905577,Human_Splice_Rec_905587,Human_Splice_Rec_905609 Human_miRNA_ID_2528265,Human_miRNA_ID_2649666,Human_miRNA_ID_2651614 RMVar_hsa_circ_119179,RMVar_hsa_circ_247440 74720 RMVar_ID_74720 Human_SNP_ID_333421367 m1A Human chr7 + 103347743 103347743 103347743 AATGCCGGATTACCTCGGTGCCGATCAGCGGAAGACCAAAGAGGATGAGAAGGACGACAAGCCCA AATGCCGGATTACCTCGGTGCCGATCAGCGGAGGACCAAAGAGGATGAGAAGGACGACAAGCCCA A G PSMC2 Ensembl:ENSG00000161057 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:103347676..103362191 32194978 MeRIP-seq:(Medium) rs747152993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253631,Human_RBP_ID_793709,Human_RBP_ID_843857,Human_RBP_ID_954843,Human_RBP_ID_1679816,Human_RBP_ID_3033883,Human_RBP_ID_4919591,Human_RBP_ID_5219222,Human_RBP_ID_7669109,Human_RBP_ID_15956824,Human_RBP_ID_21557263,Human_RBP_ID_22463264,Human_RBP_ID_26356936,Human_RBP_ID_27103404,Human_RBP_ID_27830657 Human_Splice_Rec_905567,Human_Splice_Rec_905577,Human_Splice_Rec_905587,Human_Splice_Rec_905609 Human_miRNA_ID_3106949 RMVar_hsa_circ_119179,RMVar_hsa_circ_247440 74721 RMVar_ID_74721 Human_SNP_ID_333425113 m1A Human chr7 - 103364274 103364274 103364274 TCACCGACGTATTTCTGTACAAGCTCAGATCCAATAACTCGAATGAAGCACGCATCAGTCCGATT TCACCGACGTATTTCTGTACAAGCTCAGATCCGATAACTCGAATGAAGCACGCATCAGTCCGATT T C SLC26A5 Ensembl:ENSG00000170615 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:103364226..103364376 26863196 MeRIP-seq:(Medium) rs1490293258 Functional Loss SNV dbSNP153 33..33 33 - - - 74722 RMVar_ID_74722 Human_SNP_ID_65476086 m1A Human chr2 - 30147046 30147046 30147046 CTCCCGCGGGACTCACCCTGAGCGGCGGTGAGATCCGCGGCTGCCAGCGGCTTGTCGCTCTTCAG CTCCCGCGGGACTCACCCTGAGCGGCGGTGAGCTCCGCGGCTGCCAGCGGCTTGTCGCTCTTCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:30146996..30147103 26863196 MeRIP-seq:(Medium) rs1004327602 Functional Loss SNV dbSNP153 33..33 33 - - - 74723 RMVar_ID_74723 Human_SNP_ID_65554816 m1A Human chr2 + 30447340 30447340 30447340 GGTTGTGACCCCTACGGAGCCCCAGCTTGCCCACGCACCCCACTCGGCGTCGCGCGGCGTGCCCT GGTTGTGACCCCTACGGAGCCCCAGCTTGCCCTCGCACCCCACTCGGCGTCGCGCGGCGTGCCCT A T LCLAT1 Ensembl:ENSG00000172954 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:30447289..30447398;chr2:30447291..30447670 26863196 MeRIP-seq:(Medium) rs890452699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777474,Human_RBP_ID_4623229,Human_RBP_ID_18421737 Human_Splice_Rec_231781,Human_Splice_Rec_231787,Human_Splice_Rec_231793,Human_Splice_Rec_231803,Human_Splice_Rec_231815,Human_Splice_Rec_231825,Human_Splice_Rec_231831,Human_Splice_Rec_231837,Human_Splice_Rec_231849,Human_Splice_Rec_231863 74724 RMVar_ID_74724 Human_SNP_ID_65929146 m1A Human chr2 + 31876973 31876973 31876973 GTCTACACGTTATCTCTTCCAGCCTCCTTCCAACCCATTTGCTACACTGCAGCCATATGATCTAT GTCTACACGTTATCTCTTCCAGCCTCCTTCCAGCCCATTTGCTACACTGCAGCCATATGATCTAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:31876924..31877018 26863196 MeRIP-seq:(Medium) rs1266482085 Functional Loss SNV dbSNP153 33..33 33 - - - 74725 RMVar_ID_74725 Human_SNP_ID_65936296 m1A Human chr2 - 31905921 31905921 31905921 CCTTGATGGTGTGATGGCAATATGAAGGATGGATTGGAGTTGGAAGAAATAAATAGAAATAGTGT CCTTGATGGTGTGATGGCAATATGAAGGATGGGTTGGAGTTGGAAGAAATAAATAGAAATAGTGT T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:31905885..31905990 26863196 MeRIP-seq:(Medium) rs755994318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23867752 RMVar_hsa_circ_15267,RMVar_hsa_circ_56855,RMVar_hsa_circ_273425,RMVar_hsa_circ_302142,RMVar_hsa_circ_286951,RMVar_hsa_circ_265572,RMVar_hsa_circ_275772,RMVar_hsa_circ_198235,RMVar_hsa_circ_198236,RMVar_hsa_circ_281910,RMVar_hsa_circ_301390,RMVar_hsa_circ_198237,RMVar_hsa_circ_198238,RMVar_hsa_circ_59114,RMVar_hsa_circ_347775 74726 RMVar_ID_74726 Human_SNP_ID_65961400 m1A Human chr2 - 31999209 31999209 31999209 CAAGGGCAGAACCAGGGAGACCAGTTAGGAGGAAAGGAGTAATCCAACTGTGAGATGATAGTGGC CAAGGGCAGAACCAGGGAGACCAGTTAGGAGGGAAGGAGTAATCCAACTGTGAGATGATAGTGGC T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:31999107..31999261 26863196 MeRIP-seq:(Medium) rs1263142058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 74727 RMVar_ID_74727 Human_SNP_ID_65964836 m1A Human chr2 + 32010486 32010486 32010486 GGCGGCAGCAACAATCACCACAAACTCCGGCGACCGCCGGAAGATGGGGCCCACGGCGGCCTCAC GGCGGCAGCAACAATCACCACAAACTCCGGCGTCCGCCGGAAGATGGGGCCCACGGCGGCCTCAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:32010441..32010559 26863196 MeRIP-seq:(Medium) rs1363952480 Functional Loss SNV dbSNP153 33..33 33 - - - 74728 RMVar_ID_74728 Human_SNP_ID_65964858 m1A Human chr2 - 32010582 32010582 32010582 GAGGGGAGGGGGCCGTGGGGGCGGCTCGGCGGAACCAGCCCCGGCTGGGCAGCAGCGGGGACGCC GAGGGGAGGGGGCCGTGGGGGCGGCTCGGCGGTACCAGCCCCGGCTGGGCAGCAGCGGGGACGCC T A MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32010555..32010626 26863196 MeRIP-seq:(Medium) rs1038549297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638662,Human_RBP_ID_3957742,Human_RBP_ID_9330411,Human_RBP_ID_9428616,Human_RBP_ID_18462100,Human_RBP_ID_18947717,Human_RBP_ID_19104604,Human_RBP_ID_21980527,Human_RBP_ID_26786869 74729 RMVar_ID_74729 Human_SNP_ID_65979643 m1A Human chr2 + 32063822 32063820 32063822 GCGGGAGGCGGGTTATGGCGGCGGCGGCAGTGAGAGCTGTGAATGAATTCTCCGGGTGGACGAGG GCGGGAGGCGGGTTATGGCGGCGGCGGCAGT__GAGCTGTGAATGAATTCTCCGGGTGGACGAGG TGA T SPAST Ensembl:ENSG00000021574 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32063772..32063899 26863196 MeRIP-seq:(Medium) rs1316901965 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4622338,Human_RBP_ID_18422162 RMVar_hsa_circ_94467,RMVar_hsa_circ_198253 74730 RMVar_ID_74730 Human_SNP_ID_65979646 m1A Human chr2 + 32063836 32063836 32063836 ATGGCGGCGGCGGCAGTGAGAGCTGTGAATGAATTCTCCGGGTGGACGAGGGAAGAAGAAAGGCT ATGGCGGCGGCGGCAGTGAGAGCTGTGAATGAGTTCTCCGGGTGGACGAGGGAAGAAGAAAGGCT A G SPAST Ensembl:ENSG00000021574 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:32063598..32063888 26863196 MeRIP-seq:(Medium) rs1230051542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_549626,Human_RBP_ID_4606910,Human_RBP_ID_8847743,Human_RBP_ID_9105631,Human_RBP_ID_17955619,Human_RBP_ID_23867948,Human_RBP_ID_27695072 RMVar_hsa_circ_94467,RMVar_hsa_circ_198253 74731 RMVar_ID_74731 Human_SNP_ID_65979647 m1A Human chr2 - 32063838 32063836 32063838 GGAGCCTTTCTTCTTCCCTCGTCCACCCGGAGAATTCATTCACAGCTCTCACTGCCGCCGCCGCC GGAGCCTTTCTTCTTCCCTCGTCCACCCGGAG__TTCATTCACAGCTCTCACTGCCGCCGCCGCC ATT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:32063589..32063958 26863196 MeRIP-seq:(Medium) rs1553394366 Functional Loss DEL dbSNP153 33..34 33 - - - Clinvar_Rec_341 74732 RMVar_ID_74732 Human_SNP_ID_66043179 m1A Human chr2 - 32278146 32278146 32278146 GGGGGCGGGCCCGGAGGCTGCATCTCGCGGCGACTCCCAACCGGCCGCGGTAGAAGAGGCTGCGG GGGGGCGGGCCCGGAGGCTGCATCTCGCGGCGGCTCCCAACCGGCCGCGGTAGAAGAGGCTGCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:32277934..32278165 26863410 MeRIP-seq:(Medium) rs750706985 Functional Loss SNV dbSNP153 33..33 33 - - - 74733 RMVar_ID_74733 Human_SNP_ID_66045363 m1A Human chr2 - 32284825 32284825 32284825 GGACTCTATACCCTAGCCACACTAAGCCTCTCATTTCTCTGAATGAACCTGGATTCTGTTTGTCT GGACTCTATACCCTAGCCACACTAAGCCTCTCGTTTCTCTGAATGAACCTGGATTCTGTTTGTCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:32284809..32284893 26863196 MeRIP-seq:(Medium) rs1362487726 Functional Loss SNV dbSNP153 33..33 33 - - - 74734 RMVar_ID_74734 Human_SNP_ID_66045366 m1A Human chr2 - 32284834 32284834 32284834 TCTCAATCTGGACTCTATACCCTAGCCACACTAAGCCTCTCATTTCTCTGAATGAACCTGGATTC TCTCAATCTGGACTCTATACCCTAGCCACACTGAGCCTCTCATTTCTCTGAATGAACCTGGATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:32284831..32284938 26863196 MeRIP-seq:(Medium) rs146533057 Functional Loss SNV dbSNP153 33..33 33 - - - 74735 RMVar_ID_74735 Human_SNP_ID_66066472 m1A Human chr2 - 32357254 32357248 32357254 GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCAGCCGCCATCTTCCGGCCTGCGCTCAGCACAAT GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGC______CATCTTCCGGCCTGCGCTCAGCACAAT GGCGGCT G lnc-NLRC4-4-002 RNACentral:URS00008C1097 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32357205..32357359 26863196 MeRIP-seq:(Medium) rs746777339 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_198328 74736 RMVar_ID_74736 Human_SNP_ID_66066476 m1A Human chr2 - 32357254 32357254 32357254 GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCAGCCGCCATCTTCCGGCCTGCGCTCAGCACAAT GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCCGCCGCCATCTTCCGGCCTGCGCTCAGCACAAT T G lnc-NLRC4-4-002 RNACentral:URS00008C1097 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32357205..32357359 26863196 MeRIP-seq:(Medium) rs1301148195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198328 74737 RMVar_ID_74737 Human_SNP_ID_66066534 m1A Human chr2 - 32357349 32357349 32357349 ACAGGCTGTGCAGCCCGTCGGCGTCGCAGTGCATGCAGCCGTCCCGCAGCACCAGCCACTCTGAG ACAGGCTGTGCAGCCCGTCGGCGTCGCAGTGCCTGCAGCCGTCCCGCAGCACCAGCCACTCTGAG T G lnc-NLRC4-4-002 RNACentral:URS00008C1097 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:32357298..32357377 26863196 MeRIP-seq:(Medium) rs1458393839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198328 74738 RMVar_ID_74738 Human_SNP_ID_66141086 m1A Human chr2 + 32618228 32618224 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTAT____TTTTTTTTTTACTATAGAGTGAGGGGTTGTTA TTTTA T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1559168925 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 74739 RMVar_ID_74739 Human_SNP_ID_66141089 m1A Human chr2 + 32618228 32618226 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTATTT__TTTTTTTTTTACTATAGAGTGAGGGGTTGTTA TTA T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1553539306 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 74740 RMVar_ID_74740 Human_SNP_ID_66141091 m1A Human chr2 + 32618228 32618227 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTATTTT_TTTTTTTTTTACTATAGAGTGAGGGGTTGTTA TA T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs66698122 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 74741 RMVar_ID_74741 Human_SNP_ID_66141094 m1A Human chr2 + 32618228 32618228 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTATTTTTTTTTTTTTTTACTATAGAGTGAGGGGTTGTTA A T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1043463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 74742 RMVar_ID_74742 Human_SNP_ID_66143586 m1A Human chr2 - 32628179 32628179 32628179 TCCAAAGGCGCTGAAATCTAGTGGCGACAGTTACCGTAAATACACCTGCGGCCCTAGAATTCCAT TCCAAAGGCGCTGAAATCTAGTGGCGACAGTTGCCGTAAATACACCTGCGGCCCTAGAATTCCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:32628128..32628217 26863196 MeRIP-seq:(Medium) rs1384810147 Functional Loss SNV dbSNP153 33..33 33 - - - 74743 RMVar_ID_74743 Human_SNP_ID_66219711 m1A Human chr2 - 32916241 32916241 32916241 CCCCCCCCCCCCCCCCCCCCCGCCCCCCCCCCACCCCCCCCCCCTACCCACGCCCCCCCGCAGCC CCCCCCCCCCCCCCCCCCCCCGCCCCCCCCCCCCCCCCCCCCCCTACCCACGCCCCCCCGCAGCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h chr2:32916234..32916321;chr2:32916216..32916620 26863410,26863196 MeRIP-seq:(Medium) rs199876417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1586214,Human_RBP_ID_9259468,Human_RBP_ID_9295815,Human_RBP_ID_9982688,Human_RBP_ID_17063739,Human_RBP_ID_17276029,Human_RBP_ID_17391153,Human_RBP_ID_17507339,Human_RBP_ID_18533599,Human_RBP_ID_18759653,Human_RBP_ID_21931381,Human_RBP_ID_23281687,Human_RBP_ID_24540276,Human_RBP_ID_25536842,Human_RBP_ID_26482278 74744 RMVar_ID_74744 Human_SNP_ID_66219721 m1A Human chr2 + 32916334 32916334 32916334 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG A C LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:32916170..32916671 26863196 MeRIP-seq:(Medium) rs878960983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258896,Human_RBP_ID_17068883 74745 RMVar_ID_74745 Human_SNP_ID_66219722 m1A Human chr2 + 32916334 32916334 32916334 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG A G LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:32916170..32916671 26863196 MeRIP-seq:(Medium) rs878960983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258896,Human_RBP_ID_17068883 74746 RMVar_ID_74746 Human_SNP_ID_66219723 m1A Human chr2 + 32916334 32916334 32916334 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGTGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG A T LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:32916170..32916671 26863196 MeRIP-seq:(Medium) rs878960983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258896,Human_RBP_ID_17068883 74747 RMVar_ID_74747 Human_SNP_ID_66219788 m1A Human chr2 + 32916557 32916556 32916557 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG_GGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG GA G LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEK293T,untreat control;HEPG2 cell line,total RNA Untreated chr2:32916473..32916562;chr2:32916361..32916560;chr2:32916150..32916605 26863410,26863196 MeRIP-seq:(Medium) rs1436953867 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8258898 74748 RMVar_ID_74748 Human_SNP_ID_66219789 m1A Human chr2 + 32916557 32916557 32916557 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG A C LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEK293T,untreat control;HEPG2 cell line,total RNA Untreated chr2:32916473..32916562;chr2:32916361..32916560;chr2:32916150..32916605 26863410,26863196 MeRIP-seq:(Medium) rs201491036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258898 74749 RMVar_ID_74749 Human_SNP_ID_66219790 m1A Human chr2 + 32916557 32916557 32916557 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG A G LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEK293T,untreat control;HEPG2 cell line,total RNA Untreated chr2:32916473..32916562;chr2:32916361..32916560;chr2:32916150..32916605 26863410,26863196 MeRIP-seq:(Medium) rs201491036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258898 74750 RMVar_ID_74750 Human_SNP_ID_66219791 m1A Human chr2 + 32916557 32916557 32916557 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGTGGGGGGGGGGGGGGGGGGGGGGGCGGGGGCGG A T LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEK293T,untreat control;HEPG2 cell line,total RNA Untreated chr2:32916473..32916562;chr2:32916361..32916560;chr2:32916150..32916605 26863410,26863196 MeRIP-seq:(Medium) rs201491036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258898 74751 RMVar_ID_74751 Human_SNP_ID_66219801 m1A Human chr2 + 32916598 32916597 32916598 GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGG_GGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN GA G LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:32916201..32916636;chr2:32916153..32916687;chr2:32916152..32916689;chr2:32916161..32916679;chr2:32916201..32916625;chr2:32916213..32916625 26863196 MeRIP-seq:(Medium) rs1366168222 Functional Loss DEL dbSNP153 33..33 33 - - - 74752 RMVar_ID_74752 Human_SNP_ID_66219802 m1A Human chr2 + 32916598 32916598 32916598 GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN A G LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:32916201..32916636;chr2:32916153..32916687;chr2:32916152..32916689;chr2:32916161..32916679;chr2:32916201..32916625;chr2:32916213..32916625 26863196 MeRIP-seq:(Medium) rs970905898 Functional Loss SNV dbSNP153 33..33 33 - - - 74753 RMVar_ID_74753 Human_SNP_ID_66219803 m1A Human chr2 + 32916598 32916598 32916598 GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGGAGGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN GGGGGGGGGGGGGGGCGGGGGCGGGGGGGGGGTGGGGGGGGGGGGGGGGGGGGGGGGGGGNNNNN A T LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:32916201..32916636;chr2:32916153..32916687;chr2:32916152..32916689;chr2:32916161..32916679;chr2:32916201..32916625;chr2:32916213..32916625 26863196 MeRIP-seq:(Medium) rs970905898 Functional Loss SNV dbSNP153 33..33 33 - - - 74754 RMVar_ID_74754 Human_SNP_ID_66227215 m1A Human chr2 - 32946991 32946991 32946991 GGTTGCAGCGCGCGCCGCAGCGGGGCCCGGCGAGGGTGGCCGAGAGCGAGCGAGAGCGCGCGGGA GGTTGCAGCGCGCGCCGCAGCGGGGCCCGGCGTGGGTGGCCGAGAGCGAGCGAGAGCGCGCGGGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32946946..32947334 26863196 MeRIP-seq:(Medium) rs570304318 Functional Loss SNV dbSNP153 33..33 33 - - - 74755 RMVar_ID_74755 Human_SNP_ID_66227216 m1A Human chr2 - 32946991 32946991 32946991 GGTTGCAGCGCGCGCCGCAGCGGGGCCCGGCGAGGGTGGCCGAGAGCGAGCGAGAGCGCGCGGGA GGTTGCAGCGCGCGCCGCAGCGGGGCCCGGCGCGGGTGGCCGAGAGCGAGCGAGAGCGCGCGGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32946946..32947334 26863196 MeRIP-seq:(Medium) rs570304318 Functional Loss SNV dbSNP153 33..33 33 - - - 74756 RMVar_ID_74756 Human_SNP_ID_66227302 m1A Human chr2 + 32947171 32947171 32947171 GCCGGGGTCTGGGGCCGCTCAGCTGCCCGCAGAGCCTCCTCCCTCGCCACCGACTTGGTCTCCTC GCCGGGGTCTGGGGCCGCTCAGCTGCCCGCAGCGCCTCCTCCCTCGCCACCGACTTGGTCTCCTC A C LTBP1 Ensembl:ENSG00000049323 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:32947122..32947253 26863196 MeRIP-seq:(Medium) rs1354309490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330418,Human_RBP_ID_22992231 74757 RMVar_ID_74757 Human_SNP_ID_66227414 m1A Human chr2 - 32947437 32947432 32947437 GGGGCCCGCTCAGGGGCAAGGCGCCGGCTGCCAGGCCGGGGCCCGGGTGCACCACGTAGGTGATC GGGGCCCGCTCAGGGGCAAGGCGCCGGCTGCC_____GGGGCCCGGGTGCACCACGTAGGTGATC CGGCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:32947388..32947482 26863196 MeRIP-seq:(Medium) rs1379326679 Functional Loss DEL dbSNP153 33..37 33 - - - 74758 RMVar_ID_74758 Human_SNP_ID_66227561 m1A Human chr2 + 32947730 32947730 32947730 ACCCGGCAGCCGCCCCGTTCACCAAACAAGGCAGGCAAGTTGTGCGCTCCAAGGTGCCGCAGGAG ACCCGGCAGCCGCCCCGTTCACCAAACAAGGCGGGCAAGTTGTGCGCTCCAAGGTGCCGCAGGAG A G LTBP1 Ensembl:ENSG00000049323 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32947626..32947750 26863196 MeRIP-seq:(Medium) rs1393711251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_234019 74759 RMVar_ID_74759 Human_SNP_ID_66405890 m1A Human chr2 - 33585203 33585203 33585203 TGACCATGGTGGCCGAGGGGGAGGAAGAGGAAATAAGCATCAAGGAGGCTGGACAGATGGAGGGA TGACCATGGTGGCCGAGGGGGAGGAAGAGGAATTAAGCATCAAGGAGGCTGGACAGATGGAGGGA T A FAM98A Ensembl:ENSG00000119812 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:33584800..33585646 26863196 MeRIP-seq:(Medium) rs772093703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4632479,Human_RBP_ID_17657558,Human_RBP_ID_19097254,Human_RBP_ID_22452143,Human_RBP_ID_25588532 Human_miRNA_ID_2972334,Human_miRNA_ID_3005517 RMVar_hsa_circ_198713,RMVar_hsa_circ_78266,RMVar_hsa_circ_97295,RMVar_hsa_circ_114269,RMVar_hsa_circ_198714,RMVar_hsa_circ_198715 74760 RMVar_ID_74760 Human_SNP_ID_66405891 m1A Human chr2 - 33585203 33585203 33585203 TGACCATGGTGGCCGAGGGGGAGGAAGAGGAAATAAGCATCAAGGAGGCTGGACAGATGGAGGGA TGACCATGGTGGCCGAGGGGGAGGAAGAGGAAGTAAGCATCAAGGAGGCTGGACAGATGGAGGGA T C FAM98A Ensembl:ENSG00000119812 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:33584800..33585646 26863196 MeRIP-seq:(Medium) rs772093703 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4632479,Human_RBP_ID_17657558,Human_RBP_ID_19097254,Human_RBP_ID_22452143,Human_RBP_ID_25588532 Human_miRNA_ID_2972334,Human_miRNA_ID_3005517 RMVar_hsa_circ_198713,RMVar_hsa_circ_78266,RMVar_hsa_circ_97295,RMVar_hsa_circ_114269,RMVar_hsa_circ_198714,RMVar_hsa_circ_198715 74761 RMVar_ID_74761 Human_SNP_ID_66409978 m1A Human chr2 - 33599241 33599241 33599241 TGCCGGCGAAGAGGGGAGCCTGACGACTCGGAAATTTGAATACCACAGTAGCATGGAGTGTGACC TGCCGGCGAAGAGGGGAGCCTGACGACTCGGATATTTGAATACCACAGTAGCATGGAGTGTGACC T A FAM98A Ensembl:ENSG00000119812 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:33595501..33599300;chr2:33595550..33599300 26863196 MeRIP-seq:(Medium) rs556319724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1586230,Human_RBP_ID_4607720 Human_Splice_Rec_234571,Human_Splice_Rec_234591,Human_Splice_Rec_234611,Human_Splice_Rec_234619,Human_Splice_Rec_234623 74762 RMVar_ID_74762 Human_SNP_ID_66409979 m1A Human chr2 - 33599241 33599241 33599241 TGCCGGCGAAGAGGGGAGCCTGACGACTCGGAAATTTGAATACCACAGTAGCATGGAGTGTGACC TGCCGGCGAAGAGGGGAGCCTGACGACTCGGAGATTTGAATACCACAGTAGCATGGAGTGTGACC T C FAM98A Ensembl:ENSG00000119812 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:33595501..33599300;chr2:33595550..33599300 26863196 MeRIP-seq:(Medium) rs556319724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1586230,Human_RBP_ID_4607720 Human_Splice_Rec_234571,Human_Splice_Rec_234591,Human_Splice_Rec_234611,Human_Splice_Rec_234619,Human_Splice_Rec_234623 74763 RMVar_ID_74763 Human_SNP_ID_67216744 m1A Human chr2 + 36355804 36355797 36355804 CGGCGCAGGAGTGAGGCGAGCGGGGCGCGCGGAGCGGACGCCGCGGATCTTGTGCTGCGCCACCG CGGCGCAGGAGTGAGGCGAGCGGGGC_______GCGGACGCCGCGGATCTTGTGCTGCGCCACCG CGCGCGGA C CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:36355751..36356625 26863196 MeRIP-seq:(Medium) rs1274521008 Functional Loss DEL dbSNP153 27..33 33 - - - 74764 RMVar_ID_74764 Human_SNP_ID_67216752 m1A Human chr2 + 36355804 36355804 36355804 CGGCGCAGGAGTGAGGCGAGCGGGGCGCGCGGAGCGGACGCCGCGGATCTTGTGCTGCGCCACCG CGGCGCAGGAGTGAGGCGAGCGGGGCGCGCGGGGCGGACGCCGCGGATCTTGTGCTGCGCCACCG A G CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:36355751..36356625 26863196 MeRIP-seq:(Medium) rs1392603002 Functional Loss SNV dbSNP153 33..33 33 - - - 74765 RMVar_ID_74765 Human_SNP_ID_67216761 m1A Human chr2 + 36355818 36355818 36355818 GGCGAGCGGGGCGCGCGGAGCGGACGCCGCGGATCTTGTGCTGCGCCACCGCGCCCACTCGGCAG GGCGAGCGGGGCGCGCGGAGCGGACGCCGCGGGTCTTGTGCTGCGCCACCGCGCCCACTCGGCAG A G CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36355751..36356625 26863196 MeRIP-seq:(Medium) rs1034465652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4607910 74766 RMVar_ID_74766 Human_SNP_ID_67216790 m1A Human chr2 + 36355907 36355904 36355907 AGGCTGCGCCGCTGCGGGGCCGGCCGACTCGGAGGAGGAGAGGGAGGAGGCGCCGCCGGCCCGGG AGGCTGCGCCGCTGCGGGGCCGGCCGACTC___GGAGGAGAGGGAGGAGGCGCCGCCGGCCCGGG CGGA C CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:36355726..36356577 26863196 MeRIP-seq:(Medium) rs1250413943 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4607913 74767 RMVar_ID_74767 Human_SNP_ID_67216860 m1A Human chr2 - 36356092 36356092 36356092 CCCCTTCTGCGGGCCGCGCCGACCCCGAGCCCACGAGCCTTGGCGCCGGCGGCAGCTTCCCCTCC CCCCTTCTGCGGGCCGCGCCGACCCCGAGCCCGCGAGCCTTGGCGCCGGCGGCAGCTTCCCCTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:36356051..36356219 26863196 MeRIP-seq:(Medium) rs1247948878 Functional Loss SNV dbSNP153 33..33 33 - - - 74768 RMVar_ID_74768 Human_SNP_ID_67216916 m1A Human chr2 + 36356229 36356229 36356229 GGTGCGGCGGCGGCGGCGCGTGTGCCCCGCGCAGGGGAGGGCGCCCGCCCCGCTCCCGGCCCGGC GGTGCGGCGGCGGCGGCGCGTGTGCCCCGCGCGGGGGAGGGCGCCCGCCCCGCTCCCGGCCCGGC A G CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:36356105..36356278 26863410 MeRIP-seq:(Medium) rs996779162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622347,Human_RBP_ID_5239994,Human_RBP_ID_22450280 Human_miRNA_ID_2387817,Human_miRNA_ID_3030022,Human_miRNA_ID_3065394 RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720 74769 RMVar_ID_74769 Human_SNP_ID_67222971 m1A Human chr2 + 36376391 36376391 36376391 CTGTGTAAGCTGCAGGTTGAGGAGAATGTTTAAACAGTAGGCGAGCGTTCATACAGTGTCCCTGG CTGTGTAAGCTGCAGGTTGAGGAGAATGTTTACACAGTAGGCGAGCGTTCATACAGTGTCCCTGG A C CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:36376388..36376485 26863196 MeRIP-seq:(Medium) rs1483806617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_95281,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_122982,RMVar_hsa_circ_198720,RMVar_hsa_circ_119155,RMVar_hsa_circ_198729,RMVar_hsa_circ_127349,RMVar_hsa_circ_198726,RMVar_hsa_circ_198727,RMVar_hsa_circ_198725,RMVar_hsa_circ_99062,RMVar_hsa_circ_198730,RMVar_hsa_circ_198728 74770 RMVar_ID_74770 Human_SNP_ID_67230070 m1A Human chr2 + 36400173 36400173 36400173 CATTTAATCTACACTGAGAAGGAGACAAAATCAGGGAGTCAGTGATATGGAGAGTAGAGGGGAGG CATTTAATCTACACTGAGAAGGAGACAAAATCCGGGAGTCAGTGATATGGAGAGTAGAGGGGAGG A C CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36400171..36400299 26863196 MeRIP-seq:(Medium) rs1445099706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_95281,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720,RMVar_hsa_circ_119155,RMVar_hsa_circ_198729,RMVar_hsa_circ_198726,RMVar_hsa_circ_198727,RMVar_hsa_circ_99062,RMVar_hsa_circ_198728,RMVar_hsa_circ_102355,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_94285,RMVar_hsa_circ_198732,RMVar_hsa_circ_198733,RMVar_hsa_circ_96298,RMVar_hsa_circ_372785,RMVar_hsa_circ_198735,RMVar_hsa_circ_198736,RMVar_hsa_circ_373062,RMVar_hsa_circ_374265,RMVar_hsa_circ_369883,RMVar_hsa_circ_372113,RMVar_hsa_circ_330397,RMVar_hsa_circ_275079,RMVar_hsa_circ_289317,RMVar_hsa_circ_306421,RMVar_hsa_circ_270241,RMVar_hsa_circ_271000,RMVar_hsa_circ_80290,RMVar_hsa_circ_198741,RMVar_hsa_circ_198745,RMVar_hsa_circ_198747,RMVar_hsa_circ_198749,RMVar_hsa_circ_198748,RMVar_hsa_circ_198746,RMVar_hsa_circ_198743,RMVar_hsa_circ_198744,RMVar_hsa_circ_198742,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738 74771 RMVar_ID_74771 Human_SNP_ID_67230985 m1A Human chr2 + 36403549 36403549 36403549 GGCTCAGCAGAAGGGAAGGAGAGTTTAAGAGCAGCCTTGGATAGAAAAGAGAGGACGGACAGAGA GGCTCAGCAGAAGGGAAGGAGAGTTTAAGAGCGGCCTTGGATAGAAAAGAGAGGACGGACAGAGA A G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:36403542..36403894 26863196 MeRIP-seq:(Medium) rs1299858013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_95281,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720,RMVar_hsa_circ_119155,RMVar_hsa_circ_198729,RMVar_hsa_circ_198726,RMVar_hsa_circ_198727,RMVar_hsa_circ_99062,RMVar_hsa_circ_198728,RMVar_hsa_circ_102355,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_94285,RMVar_hsa_circ_198732,RMVar_hsa_circ_198733,RMVar_hsa_circ_96298,RMVar_hsa_circ_372785,RMVar_hsa_circ_198735,RMVar_hsa_circ_198736,RMVar_hsa_circ_373062,RMVar_hsa_circ_374265,RMVar_hsa_circ_369883,RMVar_hsa_circ_372113,RMVar_hsa_circ_330397,RMVar_hsa_circ_275079,RMVar_hsa_circ_289317,RMVar_hsa_circ_306421,RMVar_hsa_circ_270241,RMVar_hsa_circ_271000,RMVar_hsa_circ_80290,RMVar_hsa_circ_198741,RMVar_hsa_circ_198745,RMVar_hsa_circ_198747,RMVar_hsa_circ_198749,RMVar_hsa_circ_198748,RMVar_hsa_circ_198746,RMVar_hsa_circ_198743,RMVar_hsa_circ_198744,RMVar_hsa_circ_198742,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738 74772 RMVar_ID_74772 Human_SNP_ID_67241401 m1A Human chr2 + 36441495 36441495 36441495 GCCGGGAGAGTGCTGTGACCTCTATGAGTGCAAACCAGGTATGCACGAGCTCTGTCTCAGCAGCC GCCGGGAGAGTGCTGTGACCTCTATGAGTGCACACCAGGTATGCACGAGCTCTGTCTCAGCAGCC A C CRIM1 Ensembl:ENSG00000150938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:36396601..36442657 32194978 MeRIP-seq:(Medium) rs774686267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550125,Human_RBP_ID_18999272,Human_RBP_ID_22451218 Human_Splice_Rec_235033,Human_Splice_Rec_235063 RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_95281,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720,RMVar_hsa_circ_119155,RMVar_hsa_circ_198729,RMVar_hsa_circ_198726,RMVar_hsa_circ_198727,RMVar_hsa_circ_99062,RMVar_hsa_circ_198728,RMVar_hsa_circ_102355,RMVar_hsa_circ_98566,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_94285,RMVar_hsa_circ_198732,RMVar_hsa_circ_198733,RMVar_hsa_circ_96298,RMVar_hsa_circ_372785,RMVar_hsa_circ_198735,RMVar_hsa_circ_198736,RMVar_hsa_circ_373062,RMVar_hsa_circ_374265,RMVar_hsa_circ_369883,RMVar_hsa_circ_372113,RMVar_hsa_circ_330397,RMVar_hsa_circ_275079,RMVar_hsa_circ_289317,RMVar_hsa_circ_306421,RMVar_hsa_circ_270241,RMVar_hsa_circ_271000,RMVar_hsa_circ_80290,RMVar_hsa_circ_198741,RMVar_hsa_circ_198745,RMVar_hsa_circ_198747,RMVar_hsa_circ_198749,RMVar_hsa_circ_198748,RMVar_hsa_circ_198746,RMVar_hsa_circ_198743,RMVar_hsa_circ_198744,RMVar_hsa_circ_198742,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738,RMVar_hsa_circ_271078,RMVar_hsa_circ_291872,RMVar_hsa_circ_304850,RMVar_hsa_circ_372388,RMVar_hsa_circ_373984,RMVar_hsa_circ_370904,RMVar_hsa_circ_293097,RMVar_hsa_circ_288474,RMVar_hsa_circ_111439,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_198755,RMVar_hsa_circ_198759,RMVar_hsa_circ_198761,RMVar_hsa_circ_198763,RMVar_hsa_circ_89130,RMVar_hsa_circ_198762,RMVar_hsa_circ_198760,RMVar_hsa_circ_198757,RMVar_hsa_circ_198758,RMVar_hsa_circ_198756,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198764,RMVar_hsa_circ_198752 74773 RMVar_ID_74773 Human_SNP_ID_67241402 m1A Human chr2 + 36441495 36441495 36441495 GCCGGGAGAGTGCTGTGACCTCTATGAGTGCAAACCAGGTATGCACGAGCTCTGTCTCAGCAGCC GCCGGGAGAGTGCTGTGACCTCTATGAGTGCAGACCAGGTATGCACGAGCTCTGTCTCAGCAGCC A G CRIM1 Ensembl:ENSG00000150938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:36396601..36442657 32194978 MeRIP-seq:(Medium) rs774686267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550125,Human_RBP_ID_18999272,Human_RBP_ID_22451218 Human_Splice_Rec_235033,Human_Splice_Rec_235063 RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_95281,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720,RMVar_hsa_circ_119155,RMVar_hsa_circ_198729,RMVar_hsa_circ_198726,RMVar_hsa_circ_198727,RMVar_hsa_circ_99062,RMVar_hsa_circ_198728,RMVar_hsa_circ_102355,RMVar_hsa_circ_98566,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_94285,RMVar_hsa_circ_198732,RMVar_hsa_circ_198733,RMVar_hsa_circ_96298,RMVar_hsa_circ_372785,RMVar_hsa_circ_198735,RMVar_hsa_circ_198736,RMVar_hsa_circ_373062,RMVar_hsa_circ_374265,RMVar_hsa_circ_369883,RMVar_hsa_circ_372113,RMVar_hsa_circ_330397,RMVar_hsa_circ_275079,RMVar_hsa_circ_289317,RMVar_hsa_circ_306421,RMVar_hsa_circ_270241,RMVar_hsa_circ_271000,RMVar_hsa_circ_80290,RMVar_hsa_circ_198741,RMVar_hsa_circ_198745,RMVar_hsa_circ_198747,RMVar_hsa_circ_198749,RMVar_hsa_circ_198748,RMVar_hsa_circ_198746,RMVar_hsa_circ_198743,RMVar_hsa_circ_198744,RMVar_hsa_circ_198742,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738,RMVar_hsa_circ_271078,RMVar_hsa_circ_291872,RMVar_hsa_circ_304850,RMVar_hsa_circ_372388,RMVar_hsa_circ_373984,RMVar_hsa_circ_370904,RMVar_hsa_circ_293097,RMVar_hsa_circ_288474,RMVar_hsa_circ_111439,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_198755,RMVar_hsa_circ_198759,RMVar_hsa_circ_198761,RMVar_hsa_circ_198763,RMVar_hsa_circ_89130,RMVar_hsa_circ_198762,RMVar_hsa_circ_198760,RMVar_hsa_circ_198757,RMVar_hsa_circ_198758,RMVar_hsa_circ_198756,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198764,RMVar_hsa_circ_198752 74774 RMVar_ID_74774 Human_SNP_ID_67245310 m1A Human chr2 - 36455713 36455713 36455713 CCTAAAGATTCTATTTCCTTATAGCCATCTCCAGTGAGACTGAGAATCCCCACATCCTACTCACT CCTAAAGATTCTATTTCCTTATAGCCATCTCCTGTGAGACTGAGAATCCCCACATCCTACTCACT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:36455705..36455839 26863196 MeRIP-seq:(Medium) rs1558604824 Functional Loss SNV dbSNP153 33..33 33 - - - 74775 RMVar_ID_74775 Human_SNP_ID_67263651 m1A Human chr2 + 36522082 36522082 36522082 CAACAGCATCTTCTTTGCTGACCTATATGTTCATTTTTCCAGATCAACCTTTTCGGCCTTCCTTG CAACAGCATCTTCTTTGCTGACCTATATGTTCGTTTTTCCAGATCAACCTTTTCGGCCTTCCTTG A G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:36522076..36522125 32194978 MeRIP-seq:(Medium) rs767770023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_89605,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198766,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_372785,RMVar_hsa_circ_275079,RMVar_hsa_circ_80290,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738,RMVar_hsa_circ_291872,RMVar_hsa_circ_373984,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_126754,RMVar_hsa_circ_198755,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198752,RMVar_hsa_circ_119470,RMVar_hsa_circ_124582,RMVar_hsa_circ_114286,RMVar_hsa_circ_198768,RMVar_hsa_circ_198767,RMVar_hsa_circ_12447,RMVar_hsa_circ_198776,RMVar_hsa_circ_283755,RMVar_hsa_circ_198765,RMVar_hsa_circ_332230,RMVar_hsa_circ_104139,RMVar_hsa_circ_96900,RMVar_hsa_circ_198774,RMVar_hsa_circ_198775,RMVar_hsa_circ_371470,RMVar_hsa_circ_277596,RMVar_hsa_circ_313176,RMVar_hsa_circ_198784,RMVar_hsa_circ_198786,RMVar_hsa_circ_198787,RMVar_hsa_circ_198785,RMVar_hsa_circ_370520,RMVar_hsa_circ_97131,RMVar_hsa_circ_198799,RMVar_hsa_circ_198796,RMVar_hsa_circ_198797,RMVar_hsa_circ_326951,RMVar_hsa_circ_282278,RMVar_hsa_circ_82537,RMVar_hsa_circ_198800,RMVar_hsa_circ_127007,RMVar_hsa_circ_371567,RMVar_hsa_circ_198798,RMVar_hsa_circ_270432,RMVar_hsa_circ_75690,RMVar_hsa_circ_198807,RMVar_hsa_circ_198808,RMVar_hsa_circ_198809,RMVar_hsa_circ_198806,RMVar_hsa_circ_118006,RMVar_hsa_circ_283672,RMVar_hsa_circ_78790,RMVar_hsa_circ_198811,RMVar_hsa_circ_198812,RMVar_hsa_circ_198810,RMVar_hsa_circ_375626,RMVar_hsa_circ_198817,RMVar_hsa_circ_325688,RMVar_hsa_circ_198815,RMVar_hsa_circ_370808,RMVar_hsa_circ_83089,RMVar_hsa_circ_98512,RMVar_hsa_circ_198819,RMVar_hsa_circ_198820,RMVar_hsa_circ_198818 74776 RMVar_ID_74776 Human_SNP_ID_67267066 m1A Human chr2 + 36534376 36534372 36534376 GGAGGAGGGAAGGAAAGAGGGAGGGAAGGGGAAGGAAGGGAGGGAGGGGGAAGGAAGGAAGGGAA GGAGGAGGGAAGGAAAGAGGGAGGGAAGG____GGAAGGGAGGGAGGGGGAAGGAAGGAAGGGAA GGGAA G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:36534365..36534450 26863196 MeRIP-seq:(Medium) rs1314211500 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198766,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_372785,RMVar_hsa_circ_80290,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198738,RMVar_hsa_circ_373984,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_126754,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198752,RMVar_hsa_circ_119470,RMVar_hsa_circ_114286,RMVar_hsa_circ_198767,RMVar_hsa_circ_12447,RMVar_hsa_circ_283755,RMVar_hsa_circ_198765,RMVar_hsa_circ_104139,RMVar_hsa_circ_96900,RMVar_hsa_circ_198774,RMVar_hsa_circ_198775,RMVar_hsa_circ_371470,RMVar_hsa_circ_277596,RMVar_hsa_circ_198784,RMVar_hsa_circ_198786,RMVar_hsa_circ_198785,RMVar_hsa_circ_97131,RMVar_hsa_circ_198799,RMVar_hsa_circ_198797,RMVar_hsa_circ_326951,RMVar_hsa_circ_82537,RMVar_hsa_circ_127007,RMVar_hsa_circ_371567,RMVar_hsa_circ_198798,RMVar_hsa_circ_75690,RMVar_hsa_circ_198807,RMVar_hsa_circ_198808,RMVar_hsa_circ_198809,RMVar_hsa_circ_118006,RMVar_hsa_circ_78790,RMVar_hsa_circ_198811,RMVar_hsa_circ_198810,RMVar_hsa_circ_325688,RMVar_hsa_circ_83089,RMVar_hsa_circ_98512,RMVar_hsa_circ_198819,RMVar_hsa_circ_198820,RMVar_hsa_circ_198818,RMVar_hsa_circ_293956,RMVar_hsa_circ_198821 74777 RMVar_ID_74777 Human_SNP_ID_67267190 m1A Human chr2 + 36534667 36534667 36534667 CAGGAAGGGAAAGGAAGGGAAGGAAGGAAGGAAATACAGGAAGGAAAAGGAAGACAGGAAGAAGG CAGGAAGGGAAAGGAAGGGAAGGAAGGAAGGAGATACAGGAAGGAAAAGGAAGACAGGAAGAAGG A G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36534582..36534849 26863196 MeRIP-seq:(Medium) rs1043247985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88426,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198766,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_372785,RMVar_hsa_circ_80290,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198738,RMVar_hsa_circ_373984,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_126754,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198752,RMVar_hsa_circ_119470,RMVar_hsa_circ_114286,RMVar_hsa_circ_198767,RMVar_hsa_circ_12447,RMVar_hsa_circ_283755,RMVar_hsa_circ_198765,RMVar_hsa_circ_104139,RMVar_hsa_circ_96900,RMVar_hsa_circ_198774,RMVar_hsa_circ_198775,RMVar_hsa_circ_371470,RMVar_hsa_circ_277596,RMVar_hsa_circ_198784,RMVar_hsa_circ_198786,RMVar_hsa_circ_198785,RMVar_hsa_circ_97131,RMVar_hsa_circ_198799,RMVar_hsa_circ_198797,RMVar_hsa_circ_326951,RMVar_hsa_circ_82537,RMVar_hsa_circ_127007,RMVar_hsa_circ_371567,RMVar_hsa_circ_198798,RMVar_hsa_circ_75690,RMVar_hsa_circ_198807,RMVar_hsa_circ_198808,RMVar_hsa_circ_198809,RMVar_hsa_circ_118006,RMVar_hsa_circ_78790,RMVar_hsa_circ_198811,RMVar_hsa_circ_198810,RMVar_hsa_circ_325688,RMVar_hsa_circ_83089,RMVar_hsa_circ_98512,RMVar_hsa_circ_198819,RMVar_hsa_circ_198820,RMVar_hsa_circ_198818,RMVar_hsa_circ_293956,RMVar_hsa_circ_198821 74778 RMVar_ID_74778 Human_SNP_ID_67268603 m1A Human chr2 - 36539376 36539376 36539376 TGCCCCACCTCTTACCTCCTCCATGCTCACTGAGTTACCTCCACACAGCTCCTCCTGAACATGCA TGCCCCACCTCTTACCTCCTCCATGCTCACTGGGTTACCTCCACACAGCTCCTCCTGAACATGCA T C FEZ2 Ensembl:ENSG00000171055 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36539372..36539558 26863196 MeRIP-seq:(Medium) rs1467512375 Functional Loss SNV dbSNP153 33..33 33 - - - 74779 RMVar_ID_74779 Human_SNP_ID_67271261 m1A Human chr2 - 36547657 36547657 36547657 TCCACCACCTCTTCATCTTTTGCGACCTTTCCACTTGGTGCTTGCCTTTGGTGCACTGACCTGTT TCCACCACCTCTTCATCTTTTGCGACCTTTCCGCTTGGTGCTTGCCTTTGGTGCACTGACCTGTT T C FEZ2 Ensembl:ENSG00000171055 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:36547608..36547699 26863196 MeRIP-seq:(Medium) rs761968558 Functional Loss SNV dbSNP153 33..33 33 - - - 74780 RMVar_ID_74780 Human_SNP_ID_67285527 m1A Human chr2 + 36591002 36591002 36591002 GGCATCACATTCCCATAATTATCTGTCAGGGCATTCCAAATCCTTAAAAAGAAGAAAGCTACAAT GGCATCACATTCCCATAATTATCTGTCAGGGCGTTCCAAATCCTTAAAAAGAAGAAAGCTACAAT A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:36590951..36591075 26863196 MeRIP-seq:(Medium) rs201031669 Functional Loss SNV dbSNP153 33..33 33 - - - 74781 RMVar_ID_74781 Human_SNP_ID_67287912 m1A Human chr2 + 36597892 36597892 36597892 CGGGGCCCCGCACTCACTCGTCCCCCTGCAGGAGGCTGCGCTCCGTGATGGGCCGCACGGCCGTC CGGGGCCCCGCACTCACTCGTCCCCCTGCAGGTGGCTGCGCTCCGTGATGGGCCGCACGGCCGTC A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36597880..36597995 26863196 MeRIP-seq:(Medium) rs1417078294 Functional Loss SNV dbSNP153 33..33 33 - - - 74782 RMVar_ID_74782 Human_SNP_ID_67287964 m1A Human chr2 + 36597964 36597964 36597964 GCTCGGCGCCCGGATCCGAGGGGCGGAAGCACAGGCTCAGCTTCTCCTCCAAGCTGCAGGCCGGG GCTCGGCGCCCGGATCCGAGGGGCGGAAGCACTGGCTCAGCTTCTCCTCCAAGCTGCAGGCCGGG A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:36597850..36597991 26863196 MeRIP-seq:(Medium) rs1221602348 Functional Loss SNV dbSNP153 33..33 33 - - - 74783 RMVar_ID_74783 Human_SNP_ID_67287978 m1A Human chr2 - 36597979 36597979 36597979 CGACGGTTTCCCGGCCCCGGCCTGCAGCTTGGAGGAGAAGCTGAGCCTGTGCTTCCGCCCCTCGG CGACGGTTTCCCGGCCCCGGCCTGCAGCTTGGGGGAGAAGCTGAGCCTGTGCTTCCGCCCCTCGG T C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:36597869..36597993 26863196 MeRIP-seq:(Medium) rs1364241578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920614,Human_RBP_ID_3957771 Human_miRNA_ID_2268392 RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74784 RMVar_ID_74784 Human_SNP_ID_67288017 m1A Human chr2 - 36598009 36598009 36598009 GGAGGCGGGGGCCGAGGCGGGTGGGGGCGCCGACGGTTTCCCGGCCCCGGCCTGCAGCTTGGAGG GGAGGCGGGGGCCGAGGCGGGTGGGGGCGCCGGCGGTTTCCCGGCCCCGGCCTGCAGCTTGGAGG T C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:36597914..36598103 26863410 MeRIP-seq:(Medium) rs1323450944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74785 RMVar_ID_74785 Human_SNP_ID_67288035 m1A Human chr2 - 36598039 36598021 36598039 GAACTGTAACGCGAGCCCCGAGCCTGGGGCGGAGGCGGGGGCCGAGGCGGGTGGGGGCGCCGACG GAACTGTAACGCGAGCCCCGAGCCTGGGGCGG__________________GTGGGGGCGCCGACG CCCGCCTCGGCCCCCGCCT C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:36597994..36598120 26863196 MeRIP-seq:(Medium) rs1426108520 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74786 RMVar_ID_74786 Human_SNP_ID_67288054 m1A Human chr2 - 36598039 36598033 36598039 GAACTGTAACGCGAGCCCCGAGCCTGGGGCGGAGGCGGGGGCCGAGGCGGGTGGGGGCGCCGACG GAACTGTAACGCGAGCCCCGAGCCTGGGGCGG______GGGCCGAGGCGGGTGGGGGCGCCGACG CCCGCCT C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:36597994..36598120 26863196 MeRIP-seq:(Medium) rs1277574377 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74787 RMVar_ID_74787 Human_SNP_ID_67288064 m1A Human chr2 - 36598039 36598039 36598039 GAACTGTAACGCGAGCCCCGAGCCTGGGGCGGAGGCGGGGGCCGAGGCGGGTGGGGGCGCCGACG GAACTGTAACGCGAGCCCCGAGCCTGGGGCGGGGGCGGGGGCCGAGGCGGGTGGGGGCGCCGACG T C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:36597994..36598120 26863196 MeRIP-seq:(Medium) rs1237495370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74788 RMVar_ID_74788 Human_SNP_ID_67288101 m1A Human chr2 - 36598099 36598099 36598099 CGGGGACTGGCAGGATTTCTATGAGTTCCAGGAGCCGGCCCGGAGCCTCCTGGACCAGGAGAACT CGGGGACTGGCAGGATTTCTATGAGTTCCAGGGGCCGGCCCGGAGCCTCCTGGACCAGGAGAACT T C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:36598049..36598151 26863196 MeRIP-seq:(Medium) rs1182144755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920615,Human_RBP_ID_4623237,Human_RBP_ID_5444827,Human_RBP_ID_18422165 RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74789 RMVar_ID_74789 Human_SNP_ID_67288115 m1A Human chr2 - 36598120 36598120 36598120 CCGGGCGGCGATGGCGGCGGACGGGGACTGGCAGGATTTCTATGAGTTCCAGGAGCCGGCCCGGA CCGGGCGGCGATGGCGGCGGACGGGGACTGGCGGGATTTCTATGAGTTCCAGGAGCCGGCCCGGA T C FEZ2 Ensembl:ENSG00000171055 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:36597886..36598150 26863196 MeRIP-seq:(Medium) rs1188949696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623237,Human_RBP_ID_18422165 RMVar_hsa_circ_121114,RMVar_hsa_circ_198830 74790 RMVar_ID_74790 Human_SNP_ID_67315272 m1A Human chr2 - 36696784 36696784 36696784 AGCTAATCGAACAGTCCCATCAACCTCTCAGTACTTTGAAAAACACATTTTACACCCCCCCCCAC AGCTAATCGAACAGTCCCATCAACCTCTCAGTGCTTTGAAAAACACATTTTACACCCCCCCCCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:36696742..36696968;chr2:36696741..36696888 26863196 MeRIP-seq:(Medium) rs1245546191 Functional Loss SNV dbSNP153 33..33 33 - - - 74791 RMVar_ID_74791 Human_SNP_ID_67358147 m1A Human chr2 - 36838875 36838865 36838875 TGGTGGGCAGTTTGCTTTAAATAAATGGGATCATGTACGTTCTCTGCATCTCACATTTCTCATTT TGGTGGGCAGTTTGCTTTAAATAAATGGGATC__________TCTGCATCTCACATTTCTCATTT AGAACGTACAT A STRN Ensembl:ENSG00000115808 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1378367339 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_198831,RMVar_hsa_circ_89526 74792 RMVar_ID_74792 Human_SNP_ID_67358154 m1A Human chr2 - 36838875 36838875 36838875 TGGTGGGCAGTTTGCTTTAAATAAATGGGATCATGTACGTTCTCTGCATCTCACATTTCTCATTT TGGTGGGCAGTTTGCTTTAAATAAATGGGATCCTGTACGTTCTCTGCATCTCACATTTCTCATTT T G STRN Ensembl:ENSG00000115808 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1504 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_8930,GWAS_ID_8931,GWAS_ID_8932,GWAS_ID_8933,GWAS_ID_8934,GWAS_ID_8935,GWAS_ID_8936,GWAS_ID_8937,GWAS_ID_8938,GWAS_ID_8939,GWAS_ID_8940,GWAS_ID_8941,GWAS_ID_8942,GWAS_ID_8943,GWAS_ID_8944,GWAS_ID_8945,GWAS_ID_8946,GWAS_ID_8947,GWAS_ID_8948 RMVar_hsa_circ_198831,RMVar_hsa_circ_89526 74793 RMVar_ID_74793 Human_SNP_ID_67377884 m1A Human chr2 - 36902644 36902644 36902644 TTCAAGTGATGTCACGGACAGGGAAGATGACAAAAATCAGGACTCAGTTGTAAATGGCACAGAGG TTCAAGTGATGTCACGGACAGGGAAGATGACAGAAATCAGGACTCAGTTGTAAATGGCACAGAGG T C STRN Ensembl:ENSG00000115808 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:36902621..36902750 26863196 MeRIP-seq:(Medium) rs1174514837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1916796,Human_RBP_ID_9105988,Human_RBP_ID_9383490,Human_RBP_ID_17699015 Human_Splice_Rec_235405,Human_Splice_Rec_235439,Human_Splice_Rec_235463 RMVar_hsa_circ_33154,RMVar_hsa_circ_378047,RMVar_hsa_circ_285695,RMVar_hsa_circ_336490,RMVar_hsa_circ_350876,RMVar_hsa_circ_74814,RMVar_hsa_circ_53168,RMVar_hsa_circ_198841,RMVar_hsa_circ_376275,RMVar_hsa_circ_198840,RMVar_hsa_circ_67361,RMVar_hsa_circ_46800,RMVar_hsa_circ_198848,RMVar_hsa_circ_351624,RMVar_hsa_circ_198849,RMVar_hsa_circ_66895,RMVar_hsa_circ_273270,RMVar_hsa_circ_369113,RMVar_hsa_circ_121010,RMVar_hsa_circ_198850,RMVar_hsa_circ_198851,RMVar_hsa_circ_198852 74794 RMVar_ID_74794 Human_SNP_ID_67397159 m1A Human chr2 - 36966327 36966327 36966327 CGGGGCGGCTGCGGCGGGGGCGGCCCGAGCCCAGTACAGTCTCCCGGGGATCCTGCACTTCCTGC CGGGGCGGCTGCGGCGGGGGCGGCCCGAGCCCCGTACAGTCTCCCGGGGATCCTGCACTTCCTGC T G STRN Ensembl:ENSG00000115808 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:36966311..36966547 26863196 MeRIP-seq:(Medium) rs928484736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624222,Human_RBP_ID_5239820 Human_Splice_Rec_235397,Human_Splice_Rec_235431 74795 RMVar_ID_74795 Human_SNP_ID_67397263 m1A Human chr2 + 36966525 36966500 36966525 CGGCGCCCAGCAGCGGAGGCAACAGCGGCGGCAAGCAGCGCCTCCTCCTCCCTCCGCCGCTCCCG CGGCGCCC_________________________AGCAGCGCCTCCTCCTCCCTCCGCCGCTCCCG CAGCAGCGGAGGCAACAGCGGCGGCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:36966185..36966556 26863196 MeRIP-seq:(Medium) rs1213214905 Functional Loss DEL dbSNP153 9..33 33 - - - 74796 RMVar_ID_74796 Human_SNP_ID_67436486 m1A Human chr2 + 37096284 37096284 37096284 GATCATGACTAAGATTATTCCCAATAAAGTGGAAACTTGAAAAATGTTATTACTTCCTAGGGATA GATCATGACTAAGATTATTCCCAATAAAGTGGGAACTTGAAAAATGTTATTACTTCCTAGGGATA A G GPATCH11 Ensembl:ENSG00000152133 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs56020915 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_235572,Human_Splice_Rec_235588,Human_Splice_Rec_235600 GWAS_ID_8949,GWAS_ID_8950,GWAS_ID_8951,GWAS_ID_8952,GWAS_ID_8953,GWAS_ID_8954,GWAS_ID_8955,GWAS_ID_8956 RMVar_hsa_circ_198952,RMVar_hsa_circ_77167 74797 RMVar_ID_74797 Human_SNP_ID_67437473 m1A Human chr2 - 37100519 37100519 37100519 GGTGACATTATTGGCTTAAATTCTAAATAACTAGAAACTGTATAATAGGCAAAACTGTGAGGCAA GGTGACATTATTGGCTTAAATTCTAAATAACTGGAAACTGTATAATAGGCAAAACTGTGAGGCAA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs14041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18316747 74798 RMVar_ID_74798 Human_SNP_ID_67437474 m1A Human chr2 - 37100523 37100523 37100523 ATATGGTGACATTATTGGCTTAAATTCTAAATAACTAGAAACTGTATAATAGGCAAAACTGTGAG ATATGGTGACATTATTGGCTTAAATTCTAAATGACTAGAAACTGTATAATAGGCAAAACTGTGAG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1558401528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18316747 74799 RMVar_ID_74799 Human_SNP_ID_67437844 m1A Human chr2 - 37102164 37102164 37102164 ACGATCACAGCTCCTTGTAACCTCGAACTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCGCTTG ACGATCACAGCTCCTTGTAACCTCGAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCGCTTG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs999281622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_235672 74800 RMVar_ID_74800 Human_SNP_ID_67444810 m1A Human chr2 + 37127621 37127621 37127621 TCCTTCCACCTAGCACCCACTGCTCTGTGCCCACTCATCCATCAGGCCTCCCCACAACTGTGACC TCCTTCCACCTAGCACCCACTGCTCTGTGCCCGCTCATCCATCAGGCCTCCCCACAACTGTGACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37127484..37127738 26863196 MeRIP-seq:(Medium) rs754942424 Functional Loss SNV dbSNP153 33..33 33 - - - 74801 RMVar_ID_74801 Human_SNP_ID_67444811 m1A Human chr2 + 37127621 37127621 37127621 TCCTTCCACCTAGCACCCACTGCTCTGTGCCCACTCATCCATCAGGCCTCCCCACAACTGTGACC TCCTTCCACCTAGCACCCACTGCTCTGTGCCCTCTCATCCATCAGGCCTCCCCACAACTGTGACC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37127484..37127738 26863196 MeRIP-seq:(Medium) rs754942424 Functional Loss SNV dbSNP153 33..33 33 - - - 74802 RMVar_ID_74802 Human_SNP_ID_67447068 m1A Human chr2 - 37136224 37136224 37136224 GTCAAGAACCATGGCACTAATGGTGTTAAGGAAGTTAAGGAGTTAAGGGCTTAGAGAGAAGACAG GTCAAGAACCATGGCACTAATGGTGTTAAGGAGGTTAAGGAGTTAAGGGCTTAGAGAGAAGACAG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:37136222..37136443 26863196 MeRIP-seq:(Medium) rs958892364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13873917 RMVar_hsa_circ_8460,RMVar_hsa_circ_48602,RMVar_hsa_circ_376240,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_198953,RMVar_hsa_circ_352994,RMVar_hsa_circ_68099,RMVar_hsa_circ_66361,RMVar_hsa_circ_32277,RMVar_hsa_circ_352459,RMVar_hsa_circ_357295,RMVar_hsa_circ_122724,RMVar_hsa_circ_198955 74803 RMVar_ID_74803 Human_SNP_ID_67447069 m1A Human chr2 - 37136224 37136224 37136224 GTCAAGAACCATGGCACTAATGGTGTTAAGGAAGTTAAGGAGTTAAGGGCTTAGAGAGAAGACAG GTCAAGAACCATGGCACTAATGGTGTTAAGGACGTTAAGGAGTTAAGGGCTTAGAGAGAAGACAG T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:37136222..37136443 26863196 MeRIP-seq:(Medium) rs958892364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13873917 RMVar_hsa_circ_8460,RMVar_hsa_circ_48602,RMVar_hsa_circ_376240,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_198953,RMVar_hsa_circ_352994,RMVar_hsa_circ_68099,RMVar_hsa_circ_66361,RMVar_hsa_circ_32277,RMVar_hsa_circ_352459,RMVar_hsa_circ_357295,RMVar_hsa_circ_122724,RMVar_hsa_circ_198955 74804 RMVar_ID_74804 Human_SNP_ID_67450877 m1A Human chr2 - 37148917 37148917 37148917 TCTGACTCAGGTTTGCTTCTCTGGCGGTCTTCAGAATCAACATCCACACTTCCGTGATTATCTGC TCTGACTCAGGTTTGCTTCTCTGGCGGTCTTCGGAATCAACATCCACACTTCCGTGATTATCTGC T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:37148868..37149014;chr2:37148868..37149062 26863196 MeRIP-seq:(Medium) rs915730335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1916916,Human_RBP_ID_4623238,Human_RBP_ID_9106021,Human_RBP_ID_17956379 Human_Splice_Rec_235609,Human_Splice_Rec_235639,Human_Splice_Rec_235675,Human_Splice_Rec_235747,Human_Splice_Rec_235756,Human_Splice_Rec_235757 RMVar_hsa_circ_48602,RMVar_hsa_circ_2442,RMVar_hsa_circ_32277,RMVar_hsa_circ_49371 74805 RMVar_ID_74805 Human_SNP_ID_67452565 m1A Human chr2 - 37154879 37154879 37154879 CAGGAAAGGAGACAGAAAAGGAGTAGCTTGTCAGAACAGAAGAAAACCAGGCCCAGGTGCCATGG CAGGAAAGGAGACAGAAAAGGAGTAGCTTGTCGGAACAGAAGAAAACCAGGCCCAGGTGCCATGG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37154877..37155210 26863196 MeRIP-seq:(Medium) rs1340356850 Functional Loss SNV dbSNP153 33..33 33 - - - 74806 RMVar_ID_74806 Human_SNP_ID_67453199 m1A Human chr2 - 37156831 37156831 37156831 CCGGGGGGCCACGTACGAGGGGCTGCAGGCCCAGCCGGGGCGGGACTCGCCAATCCTGCGTCCCC CCGGGGGGCCACGTACGAGGGGCTGCAGGCCCTGCCGGGGCGGGACTCGCCAATCCTGCGTCCCC T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr2:37156821..37157033;chr2:37156829..37156936 26863196,32194978 MeRIP-seq:(Medium) rs900992897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5379310,Human_RBP_ID_19099891,Human_RBP_ID_26786878 74807 RMVar_ID_74807 Human_SNP_ID_67468678 m1A Human chr2 + 37204443 37204443 37204443 GGGCCTACAAGTGCATGCCACCACGCCAAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGCCTACAAGTGCATGCCACCACGCCAAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs978493898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 74808 RMVar_ID_74808 Human_SNP_ID_67504253 m1A Human chr2 + 37324361 37324361 37324361 GGGCCGGGCGCGGTGGTCTCCAGCGGAGCGCGAACCCAAGTTGCCCTCCGCGCGGACGCCGGAAC GGGCCGGGCGCGGTGGTCTCCAGCGGAGCGCGGACCCAAGTTGCCCTCCGCGCGGACGCCGGAAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37324349..37324521 26863196 MeRIP-seq:(Medium) rs1026770982 Functional Loss SNV dbSNP153 33..33 33 - - - 74809 RMVar_ID_74809 Human_SNP_ID_67504428 m1A Human chr2 - 37324702 37324702 37324702 CGGTACTCAGACGCTGGCGGGCGCAGTTTCTCACGACGGGCCGAGCCTGCCACTGTAAGTAGTCG CGGTACTCAGACGCTGGCGGGCGCAGTTTCTCGCGACGGGCCGAGCCTGCCACTGTAAGTAGTCG T C PRKD3 Ensembl:ENSG00000115825 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:37324692..37324788 26863196 MeRIP-seq:(Medium) rs1231564662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243511,Human_RBP_ID_4623245,Human_RBP_ID_18421740 Human_Splice_Rec_236167 74810 RMVar_ID_74810 Human_SNP_ID_67597097 m1A Human chr2 + 37646077 37646077 37646077 GGACTGAGATGCAGAACCGCTGGAGCCCCACGAGGTGTCTCCCTGGTGGACTGTCCCATTCTCCA GGACTGAGATGCAGAACCGCTGGAGCCCCACGGGGTGTCTCCCTGGTGGACTGTCCCATTCTCCA A G AC006369.1 Ensembl:ENSG00000236213 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:37646026..37646100 32194978 MeRIP-seq:(Medium) rs753845376 Functional Loss SNV dbSNP153 33..33 33 - - - 74811 RMVar_ID_74811 Human_SNP_ID_67604073 m1A Human chr2 - 37671513 37671513 37671513 CGGATAATGCGGTGAGCAGGCACCACGCCGGCAGACTCGGCTGGATCTGCGCACAGCGGCAGGGA CGGATAATGCGGTGAGCAGGCACCACGCCGGCCGACTCGGCTGGATCTGCGCACAGCGGCAGGGA T G CDC42EP3 Ensembl:ENSG00000163171 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:37671465..37671625;chr2:37671465..37671616 26863196 MeRIP-seq:(Medium) rs1286845091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4608723 Human_Splice_Rec_236253 74812 RMVar_ID_74812 Human_SNP_ID_67679121 m1A Human chr2 - 37924962 37924962 37924962 GTTCCGGCTCTCAAACCCACTCCCTCTCCCCTAGTTAAACCTTTTTCTGTGCCCTTTCTAGGCAC GTTCCGGCTCTCAAACCCACTCCCTCTCCCCTCGTTAAACCTTTTTCTGTGCCCTTTCTAGGCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37924952..37925057 26863196 MeRIP-seq:(Medium) rs1367723375 Functional Loss SNV dbSNP153 33..33 33 - - - 74813 RMVar_ID_74813 Human_SNP_ID_67679135 m1A Human chr2 + 37924992 37924992 37924992 ACTAGGGGAGAGGGAGTGGGTTTGAGAGCCGGAACGAAGCGAGCTGGCGGTGGGCGTGCGGAGTG ACTAGGGGAGAGGGAGTGGGTTTGAGAGCCGGCACGAAGCGAGCTGGCGGTGGGCGTGCGGAGTG A C RMDN2 Ensembl:ENSG00000115841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:37924968..37925041 26863196 MeRIP-seq:(Medium) rs1225548927 Functional Loss SNV dbSNP153 33..33 33 - - - 74814 RMVar_ID_74814 Human_SNP_ID_67679319 m1A Human chr2 - 37925324 37925324 37925324 GACGGACAGTAGCCCTGGAGCCCGCGGGTCCTAAGGTCCCGCGCCGCGGCCGTCGCGTCCTGACC GACGGACAGTAGCCCTGGAGCCCGCGGGTCCTGAGGTCCCGCGCCGCGGCCGTCGCGTCCTGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:37925289..37925358 26863196 MeRIP-seq:(Medium) rs894580262 Functional Loss SNV dbSNP153 33..33 33 - - - 74815 RMVar_ID_74815 Human_SNP_ID_67723231 m1A Human chr2 + 38070854 38070854 38070854 ATGGTTAGACCATAACTGAAATTCATTTTCGCAGGCTCATTTGGGTTGGCCCTGAAATCGCACTG ATGGTTAGACCATAACTGAAATTCATTTTCGCGGGCTCATTTGGGTTGGCCCTGAAATCGCACTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:38070791..38070918 26863196 MeRIP-seq:(Medium) rs1275035459 Functional Loss SNV dbSNP153 33..33 33 - - - 74816 RMVar_ID_74816 Human_SNP_ID_67725131 m1A Human chr2 + 38075979 38075979 38075979 CCAGGAGCGCTTGGATTGGGATGGGGACGGAGAAGGGTGCCTCGCTCGCCGAGCCCCGCTGCCCT CCAGGAGCGCTTGGATTGGGATGGGGACGGAGGAGGGTGCCTCGCTCGCCGAGCCCCGCTGCCCT A G CYP1B1-AS1 Ensembl:ENSG00000232973 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:38075929..38076526 26863196 MeRIP-seq:(Medium) rs1251247736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_236567,Human_Splice_Rec_236571,Human_Splice_Rec_236577,Human_Splice_Rec_236581,Human_Splice_Rec_236587,Human_Splice_Rec_236589,Human_Splice_Rec_236601,Human_Splice_Rec_236605,Human_Splice_Rec_236611,Human_Splice_Rec_236615 74817 RMVar_ID_74817 Human_SNP_ID_67757893 m1A Human chr2 - 38179233 38179233 38179233 GGAAACTGGGAGAGGAGACAGCTTTAAGAATGAGGAAGTGATCAACTATGTCAAATATTTTCGAA GGAAACTGGGAGAGGAGACAGCTTTAAGAATGGGGAAGTGATCAACTATGTCAAATATTTTCGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:38179195..38179292 26863196 MeRIP-seq:(Medium) rs1485912239 Functional Loss SNV dbSNP153 33..33 33 - - - 74818 RMVar_ID_74818 Human_SNP_ID_67768879 m1A Human chr2 - 38218178 38218178 38218178 AAGTCAAATAAAAAAGAAAGAGACAGAAAGAAAGAAAAGAGAAAGCAAGAGAGCAAGAAAGGAAG AAGTCAAATAAAAAAGAAAGAGACAGAAAGAAGGAAAAGAGAAAGCAAGAGAGCAAGAAAGGAAG T C AC009229.1 Ensembl:ENSG00000227292 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38218084..38218180 26863196 MeRIP-seq:(Medium) rs1036312209 Functional Loss SNV dbSNP153 33..33 33 - - - 74819 RMVar_ID_74819 Human_SNP_ID_67794146 m1A Human chr2 - 38297345 38297345 38297345 AATGAAAGCTACGGTTATTAATGACGAACGCTATAATAGGCATTTGAGATGCCATTTTTGGGCTC AATGAAAGCTACGGTTATTAATGACGAACGCTGTAATAGGCATTTGAGATGCCATTTTTGGGCTC T C ATL2 Ensembl:ENSG00000119787 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3213959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27011524,Human_RBP_ID_27479995 GWAS_ID_8957,GWAS_ID_8958,GWAS_ID_8959,GWAS_ID_8960,GWAS_ID_8961,GWAS_ID_8962,GWAS_ID_8963,GWAS_ID_8964,GWAS_ID_8965,GWAS_ID_8966,GWAS_ID_8967,GWAS_ID_8968,GWAS_ID_8969,GWAS_ID_8970,GWAS_ID_8971,GWAS_ID_8972,GWAS_ID_8973,GWAS_ID_8974,GWAS_ID_8975,GWAS_ID_8976,GWAS_ID_8977,GWAS_ID_8978,GWAS_ID_8979,GWAS_ID_8980,GWAS_ID_8981,GWAS_ID_8982,GWAS_ID_8983,GWAS_ID_8984,GWAS_ID_8985,GWAS_ID_8986,GWAS_ID_8987,GWAS_ID_8988,GWAS_ID_8989,GWAS_ID_8990,GWAS_ID_8991,GWAS_ID_8992,GWAS_ID_8993,GWAS_ID_8994,GWAS_ID_8995,GWAS_ID_8996,GWAS_ID_8997,GWAS_ID_8998,GWAS_ID_8999,GWAS_ID_9000,GWAS_ID_9001,GWAS_ID_9002,GWAS_ID_9003,GWAS_ID_9004,GWAS_ID_9005,GWAS_ID_9006,GWAS_ID_9007,GWAS_ID_9008,GWAS_ID_9009,GWAS_ID_9010,GWAS_ID_9011,GWAS_ID_9012,GWAS_ID_9013,GWAS_ID_9014,GWAS_ID_9015,GWAS_ID_9016 74820 RMVar_ID_74820 Human_SNP_ID_67809467 m1A Human chr2 + 38343493 38343493 38343493 TTCTTCATAACCTCATCAGAATTTACTAGGTCATCATCTTCATAATTCTCACCTAGAATTTAAAA TTCTTCATAACCTCATCAGAATTTACTAGGTCTTCATCTTCATAATTCTCACCTAGAATTTAAAA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38343442..38343578 26863196 MeRIP-seq:(Medium) rs1451886947 Functional Loss SNV dbSNP153 33..33 33 - - - 74821 RMVar_ID_74821 Human_SNP_ID_67809475 m1A Human chr2 - 38343509 38343509 38343509 TAACCAGTTTCTTTCTTTTTAAATTCTAGGTGAGAATTATGAAGATGATGACCTAGTAAATTCTG TAACCAGTTTCTTTCTTTTTAAATTCTAGGTGCGAATTATGAAGATGATGACCTAGTAAATTCTG T G ATL2 Ensembl:ENSG00000119787 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:38343476..38343565 26863196 MeRIP-seq:(Medium) rs1298214289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1917277,Human_RBP_ID_9386356 Human_Splice_Rec_236756,Human_Splice_Rec_236848,Human_Splice_Rec_236894,Human_Splice_Rec_236954,Human_Splice_Rec_236980,Human_Splice_Rec_236986,Human_Splice_Rec_236992,Human_Splice_Rec_236996 RMVar_hsa_circ_47248,RMVar_hsa_circ_362471,RMVar_hsa_circ_351631,RMVar_hsa_circ_199009,RMVar_hsa_circ_13615,RMVar_hsa_circ_55003,RMVar_hsa_circ_64461,RMVar_hsa_circ_199013,RMVar_hsa_circ_288173 74822 RMVar_ID_74822 Human_SNP_ID_67821159 m1A Human chr2 + 38377209 38377209 38377209 GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCACAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCGCAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38377097..38377275 26863196 MeRIP-seq:(Medium) rs3731847 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 74823 RMVar_ID_74823 Human_SNP_ID_67821160 m1A Human chr2 + 38377209 38377209 38377209 GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCACAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCTCAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38377097..38377275 26863196 MeRIP-seq:(Medium) rs3731847 Functional Loss SNV dbSNP153 33..33 33 - - - 74824 RMVar_ID_74824 Human_SNP_ID_67821191 m1A Human chr2 - 38377240 38377240 38377240 AATCGGTACAAGATGGCGGAGGGGGACGAGGCAGCGCGAGGGCAGCAACCGCACCAGGGGCTGTG AATCGGTACAAGATGGCGGAGGGGGACGAGGCGGCGCGAGGGCAGCAACCGCACCAGGGGCTGTG T C ATL2 Ensembl:ENSG00000119787 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:38377103..38377275 26863196 MeRIP-seq:(Medium) rs1388565942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243559,Human_RBP_ID_13878275,Human_RBP_ID_18421742,Human_RBP_ID_22449779,Human_RBP_ID_22996802,Human_RBP_ID_26770341,Human_RBP_ID_27840013 Human_Splice_Rec_236755,Human_Splice_Rec_236779,Human_Splice_Rec_236825,Human_Splice_Rec_236847,Human_Splice_Rec_236871,Human_Splice_Rec_236945,Human_Splice_Rec_236953,Human_Splice_Rec_236965,Human_Splice_Rec_236979,Human_Splice_Rec_236983,Human_Splice_Rec_236993 74825 RMVar_ID_74825 Human_SNP_ID_67821241 m1A Human chr2 - 38377312 38377311 38377312 GGCCACCCCGCCGGCTCCCGGGAGGTTGATAAAGCGGCGGCGGCGTTTGACGTCAGTGGGGAGTT GGCCACCCCGCCGGCTCCCGGGAGGTTGATAA_GCGGCGGCGGCGTTTGACGTCAGTGGGGAGTT CT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:38377307..38377389 26863410 MeRIP-seq:(Medium) rs1453572287 Functional Loss DEL dbSNP153 33..33 33 - - - 74826 RMVar_ID_74826 Human_SNP_ID_67852617 m1A Human chr2 + 38482059 38482059 38482059 CATGATGCGCAAGGCCATCCGAGGGCACCTGGAAAACAACCCAGCTCTGGAGAAACTGCTGCCTC CATGATGCGCAAGGCCATCCGAGGGCACCTGGCAAACAACCCAGCTCTGGAGAAACTGCTGCCTC A C RPLP0P6 Ensembl:ENSG00000213553 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1289728185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550620,Human_RBP_ID_1064024,Human_RBP_ID_5295132,Human_RBP_ID_5652085,Human_RBP_ID_8203224,Human_RBP_ID_9113848,Human_RBP_ID_17393175,Human_RBP_ID_17618270,Human_RBP_ID_17699901,Human_RBP_ID_18193275,Human_RBP_ID_19105649,Human_RBP_ID_22425693,Human_RBP_ID_26818381 Human_miRNA_ID_1889810,Human_miRNA_ID_1891991 74827 RMVar_ID_74827 Human_SNP_ID_67887924 m1A Human chr2 + 38602823 38602823 38602823 AAGCGCGGACGGACTGAGGGGGGCGCCCCGGGAGGAAGCTCTGGAGCGGCCGCTCCTCTCAATTA AAGCGCGGACGGACTGAGGGGGGCGCCCCGGGGGGAAGCTCTGGAGCGGCCGCTCCTCTCAATTA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:38602757..38602908 26863410 MeRIP-seq:(Medium) rs1478780874 Functional Loss SNV dbSNP153 33..33 33 - - - 74828 RMVar_ID_74828 Human_SNP_ID_67887925 m1A Human chr2 + 38602823 38602823 38602823 AAGCGCGGACGGACTGAGGGGGGCGCCCCGGGAGGAAGCTCTGGAGCGGCCGCTCCTCTCAATTA AAGCGCGGACGGACTGAGGGGGGCGCCCCGGGTGGAAGCTCTGGAGCGGCCGCTCCTCTCAATTA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:38602757..38602908 26863410 MeRIP-seq:(Medium) rs1478780874 Functional Loss SNV dbSNP153 33..33 33 - - - 74829 RMVar_ID_74829 Human_SNP_ID_67887958 m1A Human chr2 + 38602864 38602864 38602864 TGGAGCGGCCGCTCCTCTCAATTACCGAGCCAACATTCAGCCTCTCCCTCCTCCTCCTCCGTCTC TGGAGCGGCCGCTCCTCTCAATTACCGAGCCAGCATTCAGCCTCTCCCTCCTCCTCCTCCGTCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38602409..38602957 26863196 MeRIP-seq:(Medium) rs1182167884 Functional Loss SNV dbSNP153 33..33 33 - - - 74830 RMVar_ID_74830 Human_SNP_ID_67906574 m1A Human chr2 + 38666151 38666151 38666151 AGTTTGAAGAGCGGGCAGTGGCTGCACACGCCAAACTTTCCCTATGGCTTCGGTGACCAGGGCCG AGTTTGAAGAGCGGGCAGTGGCTGCACACGCCGAACTTTCCCTATGGCTTCGGTGACCAGGGCCG A G GALM Ensembl:ENSG00000143891 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:38666058..38666269 26863196 MeRIP-seq:(Medium) rs1254896447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623249 74831 RMVar_ID_74831 Human_SNP_ID_67906575 m1A Human chr2 + 38666151 38666151 38666151 AGTTTGAAGAGCGGGCAGTGGCTGCACACGCCAAACTTTCCCTATGGCTTCGGTGACCAGGGCCG AGTTTGAAGAGCGGGCAGTGGCTGCACACGCCTAACTTTCCCTATGGCTTCGGTGACCAGGGCCG A T GALM Ensembl:ENSG00000143891 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:38666058..38666269 26863196 MeRIP-seq:(Medium) rs1254896447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623249 74832 RMVar_ID_74832 Human_SNP_ID_67906595 m1A Human chr2 + 38666177 38666177 38666177 CACGCCAAACTTTCCCTATGGCTTCGGTGACCAGGGCCGTGTTTGGAGAGCTGCCCTCGGGAGGA CACGCCAAACTTTCCCTATGGCTTCGGTGACCGGGGCCGTGTTTGGAGAGCTGCCCTCGGGAGGA A G GALM Ensembl:ENSG00000143891 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38666127..38666264 26863196 MeRIP-seq:(Medium) rs1283061113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623250 74833 RMVar_ID_74833 Human_SNP_ID_67909805 m1A Human chr2 + 38675962 38675962 38675962 CATACTTTGGAGCAGTTATTGGGAGGGTGGCCAACCGAATCGCCAAAGGAACCTTCAAGGTGGAT CATACTTTGGAGCAGTTATTGGGAGGGTGGCCGACCGAATCGCCAAAGGAACCTTCAAGGTGGAT A G GALM Ensembl:ENSG00000143891 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:38666158..38675968 32194978 MeRIP-seq:(Medium) rs140986269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915435,Human_RBP_ID_9383519,Human_RBP_ID_26339223,Human_RBP_ID_27818407 Human_Splice_Rec_237276,Human_Splice_Rec_237282,Human_Splice_Rec_237300 RMVar_hsa_circ_199034,RMVar_hsa_circ_353426,RMVar_hsa_circ_361426,RMVar_hsa_circ_347579 74834 RMVar_ID_74834 Human_SNP_ID_67909830 m1A Human chr2 - 38676004 38676004 38676004 ACTGTTGGGTTCCTTGTTAATGGCCAGGTGATACTCCTTCCCATCCACCTTGAAGGTTCCTTTGG ACTGTTGGGTTCCTTGTTAATGGCCAGGTGATCCTCCTTCCCATCCACCTTGAAGGTTCCTTTGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38675856..38676010 26863196 MeRIP-seq:(Medium) rs1281806205 Functional Loss SNV dbSNP153 33..33 33 - - - 74835 RMVar_ID_74835 Human_SNP_ID_67918966 m1A Human chr2 - 38709022 38709022 38709022 CTGCTCCTCCTCTCTGATAAAACCCCAACTTCAGGTCATCCCACCATTTGCCTTCTCTGCTCCTG CTGCTCCTCCTCTCTGATAAAACCCCAACTTCGGGTCATCCCACCATTTGCCTTCTCTGCTCCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38709002..38709229 26863196 MeRIP-seq:(Medium) rs1378886743 Functional Loss SNV dbSNP153 33..33 33 - - - 74836 RMVar_ID_74836 Human_SNP_ID_67919718 m1A Human chr2 + 38711733 38711731 38711734 CATCATCATCCATCACCATCACTATCAACACCATCATCATTAACATCACCATCACTATCACCACC CATCATCATCCATCACCATCACTATCAACAC___CATCATTAACATCACCATCACTATCACCACC CCAT C GALM Ensembl:ENSG00000143891 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38711717..38711818 26863196 MeRIP-seq:(Medium) rs1217257234 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_204780,Human_RBP_ID_264357,Human_RBP_ID_1067631,Human_RBP_ID_2642647,Human_RBP_ID_9428628,Human_RBP_ID_17658041,Human_RBP_ID_24533649,Human_RBP_ID_26760356 74837 RMVar_ID_74837 Human_SNP_ID_67919784 m1A Human chr2 + 38711805 38711803 38711806 CCATCACTGTCACCACCATCACCATCACCATCACCATCATCATCATCACTATCACCACCATCATC CCATCACTGTCACCACCATCACCATCACCAT___CATCATCATCATCACTATCACCACCATCATC TCAC T GALM Ensembl:ENSG00000143891 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38711706..38711890 26863196 MeRIP-seq:(Medium) rs1558591957 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8685,Human_RBP_ID_264357 74838 RMVar_ID_74838 Human_SNP_ID_67919786 m1A Human chr2 + 38711805 38711805 38711805 CCATCACTGTCACCACCATCACCATCACCATCACCATCATCATCATCACTATCACCACCATCATC CCATCACTGTCACCACCATCACCATCACCATCGCCATCATCATCATCACTATCACCACCATCATC A G GALM Ensembl:ENSG00000143891 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38711706..38711890 26863196 MeRIP-seq:(Medium) rs113710394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8685,Human_RBP_ID_264357 74839 RMVar_ID_74839 Human_SNP_ID_67929717 m1A Human chr2 - 38745060 38745060 38745060 ACATTATTATAAGGGATTTGTGATGTCTGTAAAGTGTAACCTAGGAAAGATAATTCAACCATCTA ACATTATTATAAGGGATTTGTGATGTCTGTAAGGTGTAACCTAGGAAAGATAATTCAACCATCTA T C SRSF7 Ensembl:ENSG00000115875 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1217514390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58089,Human_RBP_ID_550744,Human_RBP_ID_1196046,Human_RBP_ID_1586718,Human_RBP_ID_1917370,Human_RBP_ID_2674605,Human_RBP_ID_3625335,Human_RBP_ID_6918230,Human_RBP_ID_8518668,Human_RBP_ID_9106182,Human_RBP_ID_9984184,Human_RBP_ID_13880891,Human_RBP_ID_17699069,Human_RBP_ID_18760492,Human_RBP_ID_22251354,Human_RBP_ID_22505609,Human_RBP_ID_23211508,Human_RBP_ID_23871135,Human_RBP_ID_24421645,Human_RBP_ID_24489325,Human_RBP_ID_26482990,Human_RBP_ID_27011601,Human_RBP_ID_27695837 Human_miRNA_ID_2568886 RMVar_hsa_circ_87262,RMVar_hsa_circ_199037 74840 RMVar_ID_74840 Human_SNP_ID_67932274 m1A Human chr2 + 38751261 38751261 38751261 CTCCTCCGTACCGCCCGTAACGCGACATGATGACAGACCCGCGTGCTCGGCTCTTTAGCAAGCAG CTCCTCCGTACCGCCCGTAACGCGACATGATGCCAGACCCGCGTGCTCGGCTCTTTAGCAAGCAG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:38751226..38751375 26863196 MeRIP-seq:(Medium) rs369776538 Functional Loss SNV dbSNP153 33..33 33 - - - 74841 RMVar_ID_74841 Human_SNP_ID_67932275 m1A Human chr2 + 38751261 38751261 38751261 CTCCTCCGTACCGCCCGTAACGCGACATGATGACAGACCCGCGTGCTCGGCTCTTTAGCAAGCAG CTCCTCCGTACCGCCCGTAACGCGACATGATGGCAGACCCGCGTGCTCGGCTCTTTAGCAAGCAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:38751226..38751375 26863196 MeRIP-seq:(Medium) rs369776538 Functional Loss SNV dbSNP153 33..33 33 - - - 74842 RMVar_ID_74842 Human_SNP_ID_67932283 m1A Human chr2 - 38751272 38751271 38751272 AGCCCTGGGCGCTGCTTGCTAAAGAGCCGAGCACGCGGGTCTGTCATCATGTCGCGTTACGGGCG AGCCCTGGGCGCTGCTTGCTAAAGAGCCGAGC_CGCGGGTCTGTCATCATGTCGCGTTACGGGCG GT G SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:38751226..38751375 26863410 MeRIP-seq:(Medium) rs1278995487 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550755,Human_RBP_ID_1586762,Human_RBP_ID_4609060,Human_RBP_ID_5322049,Human_RBP_ID_5423053,Human_RBP_ID_9330424,Human_RBP_ID_13881225,Human_RBP_ID_18421744,Human_RBP_ID_18760517,Human_RBP_ID_23871181,Human_RBP_ID_26818407,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74843 RMVar_ID_74843 Human_SNP_ID_67932284 m1A Human chr2 - 38751272 38751272 38751272 AGCCCTGGGCGCTGCTTGCTAAAGAGCCGAGCACGCGGGTCTGTCATCATGTCGCGTTACGGGCG AGCCCTGGGCGCTGCTTGCTAAAGAGCCGAGCGCGCGGGTCTGTCATCATGTCGCGTTACGGGCG T C SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:38751226..38751375 26863410 MeRIP-seq:(Medium) rs768408257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550755,Human_RBP_ID_1586762,Human_RBP_ID_4609060,Human_RBP_ID_5322049,Human_RBP_ID_5423053,Human_RBP_ID_9330424,Human_RBP_ID_13881225,Human_RBP_ID_18421744,Human_RBP_ID_18760517,Human_RBP_ID_23871181,Human_RBP_ID_26818407,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74844 RMVar_ID_74844 Human_SNP_ID_67932286 m1A Human chr2 + 38751288 38751273 38751289 TGATGACAGACCCGCGTGCTCGGCTCTTTAGCAAGCAGCGCCCAGGGCTCGAGTGACGCAAAAGC TGATGACAGACCCGCGTG________________GCAGCGCCCAGGGCTCGAGTGACGCAAAAGC GCTCGGCTCTTTAGCAA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr2:38751226..38751350 26863410 MeRIP-seq:(Medium) rs1265960839 Functional Loss DEL dbSNP153 19..34 33 - - - 74845 RMVar_ID_74845 Human_SNP_ID_67932294 m1A Human chr2 - 38751280 38751280 38751280 GTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCCGAGCACGCGGGTCTGTCATCATGTCGCGT GTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGGGCCGAGCACGCGGGTCTGTCATCATGTCGCGT T C SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:38751226..38751350 32194978 MeRIP-seq:(Medium) rs1473555434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550755,Human_RBP_ID_1586762,Human_RBP_ID_4609060,Human_RBP_ID_5275712,Human_RBP_ID_5322049,Human_RBP_ID_8518693,Human_RBP_ID_9330424,Human_RBP_ID_13881225,Human_RBP_ID_18421744,Human_RBP_ID_18760517,Human_RBP_ID_22076218,Human_RBP_ID_22251377,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818407,Human_RBP_ID_27011643,Human_RBP_ID_27290136,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74846 RMVar_ID_74846 Human_SNP_ID_67932307 m1A Human chr2 - 38751309 38751292 38751309 GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTC_________________TGCTTGCTAAAGAGCC AGCGCCCAGGGCTCGAGT A SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:38751067..38751375;chr2:38751210..38751350;chr2:38751051..38751375 26863196 MeRIP-seq:(Medium) rs747402341 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550758,Human_RBP_ID_1196050,Human_RBP_ID_1301047,Human_RBP_ID_1586765,Human_RBP_ID_4609060,Human_RBP_ID_6918317,Human_RBP_ID_8518694,Human_RBP_ID_8848191,Human_RBP_ID_9106189,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421744,Human_RBP_ID_22076218,Human_RBP_ID_22452151,Human_RBP_ID_22992642,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2756038 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74847 RMVar_ID_74847 Human_SNP_ID_67932330 m1A Human chr2 + 38751307 38751307 38751307 TCGGCTCTTTAGCAAGCAGCGCCCAGGGCTCGAGTGACGCAAAAGCTGACACACACCTTCACCCG TCGGCTCTTTAGCAAGCAGCGCCCAGGGCTCGCGTGACGCAAAAGCTGACACACACCTTCACCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:38751077..38751375;chr2:38751160..38751375 26863196 MeRIP-seq:(Medium) rs764701297 Functional Loss SNV dbSNP153 33..33 33 - - - 74848 RMVar_ID_74848 Human_SNP_ID_67932331 m1A Human chr2 + 38751307 38751307 38751307 TCGGCTCTTTAGCAAGCAGCGCCCAGGGCTCGAGTGACGCAAAAGCTGACACACACCTTCACCCG TCGGCTCTTTAGCAAGCAGCGCCCAGGGCTCGTGTGACGCAAAAGCTGACACACACCTTCACCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:38751077..38751375;chr2:38751160..38751375 26863196 MeRIP-seq:(Medium) rs764701297 Functional Loss SNV dbSNP153 33..33 33 - - - 74849 RMVar_ID_74849 Human_SNP_ID_67932333 m1A Human chr2 - 38751309 38751309 38751309 GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCTCTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC T A SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:38751067..38751375;chr2:38751210..38751350;chr2:38751051..38751375 26863196 MeRIP-seq:(Medium) rs117377682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550758,Human_RBP_ID_1196050,Human_RBP_ID_1301047,Human_RBP_ID_1586765,Human_RBP_ID_4609060,Human_RBP_ID_6918317,Human_RBP_ID_8518694,Human_RBP_ID_8848191,Human_RBP_ID_9106189,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421744,Human_RBP_ID_22076218,Human_RBP_ID_22452151,Human_RBP_ID_22992642,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2756038 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74850 RMVar_ID_74850 Human_SNP_ID_67932334 m1A Human chr2 - 38751309 38751309 38751309 GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCCCTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC T G SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:38751067..38751375;chr2:38751210..38751350;chr2:38751051..38751375 26863196 MeRIP-seq:(Medium) rs117377682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_550758,Human_RBP_ID_1196050,Human_RBP_ID_1301047,Human_RBP_ID_1586765,Human_RBP_ID_4609060,Human_RBP_ID_6918317,Human_RBP_ID_8518694,Human_RBP_ID_8848191,Human_RBP_ID_9106189,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421744,Human_RBP_ID_22076218,Human_RBP_ID_22452151,Human_RBP_ID_22992642,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2756038 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74851 RMVar_ID_74851 Human_SNP_ID_67932346 m1A Human chr2 - 38751321 38751321 38751321 GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCGGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT T C SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38751060..38751375 26863196 MeRIP-seq:(Medium) rs570745972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_1196050,Human_RBP_ID_1586765,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74852 RMVar_ID_74852 Human_SNP_ID_67932347 m1A Human chr2 - 38751321 38751321 38751321 GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCCGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT T G SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38751060..38751375 26863196 MeRIP-seq:(Medium) rs570745972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_1196050,Human_RBP_ID_1586765,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74853 RMVar_ID_74853 Human_SNP_ID_67932370 m1A Human chr2 - 38751333 38751333 38751333 CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGTAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC T A SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs182579979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2428154,Human_miRNA_ID_2487953,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74854 RMVar_ID_74854 Human_SNP_ID_67932371 m1A Human chr2 - 38751333 38751333 38751333 CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGGAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC T C SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs182579979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2428154,Human_miRNA_ID_2487953,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74855 RMVar_ID_74855 Human_SNP_ID_67932372 m1A Human chr2 - 38751333 38751333 38751333 CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGCAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC T G SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs182579979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58102,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2428154,Human_miRNA_ID_2487953,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 74856 RMVar_ID_74856 Human_SNP_ID_67950628 m1A Human chr2 - 38804651 38804651 38804651 AGAGGGATGATCAAGGGTGAGAGTGGTGGGAGATGCACGGGGACGAGTAGGCAGGGGTGGGGTAG AGAGGGATGATCAAGGGTGAGAGTGGTGGGAGGTGCACGGGGACGAGTAGGCAGGGGTGGGGTAG T C DHX57 Ensembl:ENSG00000163214 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:38804643..38804728 26863196 MeRIP-seq:(Medium) rs1187163696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40340,RMVar_hsa_circ_310222,RMVar_hsa_circ_372107,RMVar_hsa_circ_199047,RMVar_hsa_circ_272520,RMVar_hsa_circ_300487,RMVar_hsa_circ_43509,RMVar_hsa_circ_199049,RMVar_hsa_circ_199051,RMVar_hsa_circ_10394,RMVar_hsa_circ_199050 74857 RMVar_ID_74857 Human_SNP_ID_67969581 m1A Human chr2 + 38868309 38868309 38868309 ACCACCACCGCCACCGCCACCACTCCCATGAGATTTACTGGCGTGACTCCTGCCTCCTCTTCCTC ACCACCACCGCCACCGCCACCACTCCCATGAGGTTTACTGGCGTGACTCCTGCCTCCTCTTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:38868259..38868334 26863196 MeRIP-seq:(Medium) rs779045038 Functional Loss SNV dbSNP153 33..33 33 - - - 74858 RMVar_ID_74858 Human_SNP_ID_67969600 m1A Human chr2 - 38868358 38868358 38868358 AGAAGAAAAGGCAAGCCAGGCAAAGGAGGTGGAAAAGGGTCTTCTAGAGGAGGAAGAGGAGGCAG AGAAGAAAAGGCAAGCCAGGCAAAGGAGGTGGCAAAGGGTCTTCTAGAGGAGGAAGAGGAGGCAG T G DHX57 Ensembl:ENSG00000163214 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:38868204..38868414 26863196 MeRIP-seq:(Medium) rs769574303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8518710,Human_RBP_ID_19001537 Human_Splice_Rec_237496,Human_Splice_Rec_237568,Human_Splice_Rec_237668 RMVar_hsa_circ_3658,RMVar_hsa_circ_25982 74859 RMVar_ID_74859 Human_SNP_ID_67969603 m1A Human chr2 + 38868361 38868361 38868361 CCTCCTCTTCCTCCTCTAGAAGACCCTTTTCCACCTCCTTTGCCTGGCTTGCCTTTTCTTCTTAC CCTCCTCTTCCTCCTCTAGAAGACCCTTTTCCGCCTCCTTTGCCTGGCTTGCCTTTTCTTCTTAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38868173..38868421 26863196 MeRIP-seq:(Medium) rs770339884 Functional Loss SNV dbSNP153 33..33 33 - - - 74860 RMVar_ID_74860 Human_SNP_ID_68024427 m1A Human chr2 - 39070424 39070424 39070424 GGGTGGAGGAATGGAGGAAGATATGGAACTCTACAAGGACATGGAAAAGGAATAAGGAAATTAGG GGGTGGAGGAATGGAGGAAGATATGGAACTCTGCAAGGACATGGAAAAGGAATAAGGAAATTAGG T C SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:39070422..39070547 26863196 MeRIP-seq:(Medium) rs945787380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117146,RMVar_hsa_circ_199095,RMVar_hsa_circ_199101,RMVar_hsa_circ_199102 74861 RMVar_ID_74861 Human_SNP_ID_68035169 m1A Human chr2 - 39107448 39107448 39107448 GAGAGGTAAGGAAGGAAGGAACTTTGAGTGAAAGTGTCTTAGACTGTAGTGCAATACTAAGGAAA GAGAGGTAAGGAAGGAAGGAACTTTGAGTGAAGGTGTCTTAGACTGTAGTGCAATACTAAGGAAA T C SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:39107446..39107580 26863196 MeRIP-seq:(Medium) rs1325773820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9984511,Human_RBP_ID_13882963,Human_RBP_ID_23893126 RMVar_hsa_circ_117146,RMVar_hsa_circ_199095,RMVar_hsa_circ_199101 74862 RMVar_ID_74862 Human_SNP_ID_68039300 m1A Human chr2 - 39120425 39120425 39120425 CCCCTCTCCCCGCCCAGAGGCGCCCCGGGGGCACCATGCAGGCGCAGCAGCTGCCCTACGAGTTT CCCCTCTCCCCGCCCAGAGGCGCCCCGGGGGCGCCATGCAGGCGCAGCAGCTGCCCTACGAGTTT T C SOS1 Ensembl:ENSG00000115904 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:39120387..39121039;chr2:39120376..39121039 26863196 MeRIP-seq:(Medium) rs1457481444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330425,Human_RBP_ID_18443538 Human_Splice_Rec_237853,Human_Splice_Rec_237897 RMVar_hsa_circ_117146,RMVar_hsa_circ_199095 74863 RMVar_ID_74863 Human_SNP_ID_68039412 m1A Human chr2 - 39120603 39120597 39120603 CCACGGCTGGTACCTGTGTCGGGTGGGTGGCCAGGCGCGGGCCTCGCCCCCCAGCCCCCTCGCCA CCACGGCTGGTACCTGTGTCGGGTGGGTGGCC______GGGCCTCGCCCCCCAGCCCCCTCGCCA CGCGCCT C SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:39120506..39120667 26863196 MeRIP-seq:(Medium) rs1400819715 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4609238,Human_RBP_ID_17670347,Human_RBP_ID_18422662,Human_RBP_ID_18493300 74864 RMVar_ID_74864 Human_SNP_ID_68039511 m1A Human chr2 - 39120862 39120862 39120862 CCCCGCCCGGGGCTCTTGCGTTTCGGAGTCCCAACTACGCGGAGCGGGCGCCGCGGCCGGAGCGT CCCCGCCCGGGGCTCTTGCGTTTCGGAGTCCCCACTACGCGGAGCGGGCGCCGCGGCCGGAGCGT T G SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:39120326..39120975 26863196 MeRIP-seq:(Medium) rs1291713070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778035,Human_RBP_ID_5502210,Human_RBP_ID_9330428,Human_RBP_ID_18443539 74865 RMVar_ID_74865 Human_SNP_ID_68039520 m1A Human chr2 - 39120901 39120890 39120901 GTCCTTCCCCTTCCCCGCGAGACCTCCGCCCCAGCTCCGCCCCGCCCGGGGCTCTTGCGTTTCGG GTCCTTCCCCTTCCCCGCGAGACCTCCGCCCC___________GCCCGGGGCTCTTGCGTTTCGG CGGGGCGGAGCT C SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:39120859..39120962 32194978 MeRIP-seq:(Medium) rs149710810 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_4632778,Human_RBP_ID_18470784,Human_RBP_ID_20570782,Human_RBP_ID_25541003,Human_RBP_ID_26786199 Clinvar_Rec_342,Clinvar_Rec_343 GWAS_ID_9017,GWAS_ID_9018,GWAS_ID_9019,GWAS_ID_9020,GWAS_ID_9021,GWAS_ID_9022,GWAS_ID_9023,GWAS_ID_9024,GWAS_ID_9025,GWAS_ID_9026,GWAS_ID_9027,GWAS_ID_9028,GWAS_ID_9029,GWAS_ID_9030,GWAS_ID_9031,GWAS_ID_9032,GWAS_ID_9033,GWAS_ID_9034,GWAS_ID_9035,GWAS_ID_9036,GWAS_ID_9037,GWAS_ID_9038,GWAS_ID_9039,GWAS_ID_9040,GWAS_ID_9041,GWAS_ID_9042,GWAS_ID_9043,GWAS_ID_9044,GWAS_ID_9045,GWAS_ID_9046,GWAS_ID_9047,GWAS_ID_9048,GWAS_ID_9049,GWAS_ID_9050,GWAS_ID_9051,GWAS_ID_9052,GWAS_ID_9053,GWAS_ID_9054,GWAS_ID_9055,GWAS_ID_9056,GWAS_ID_9057,GWAS_ID_9058,GWAS_ID_9059,GWAS_ID_9060,GWAS_ID_9061,GWAS_ID_9062,GWAS_ID_9063,GWAS_ID_9064,GWAS_ID_9065,GWAS_ID_9066,GWAS_ID_9067,GWAS_ID_9068 74866 RMVar_ID_74866 Human_SNP_ID_68128961 m1A Human chr2 - 39437110 39437110 39437110 GAGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGAGCCGGGTGATTGTGACCGCCGGGGGAGCCGGG GAGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGGGCCGGGTGATTGTGACCGCCGGGGGAGCCGGG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:39436982..39437275 26863196 MeRIP-seq:(Medium) rs943735616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9386394,Human_RBP_ID_18421746,Human_RBP_ID_22597969,Human_RBP_ID_22997134,Human_RBP_ID_26339233,Human_RBP_ID_27817027 74867 RMVar_ID_74867 Human_SNP_ID_68128980 m1A Human chr2 - 39437141 39437141 39437141 CCGCTTGTCGTCGTCCGCAGCGGCGTGAGGGGAGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGAG CCGCTTGTCGTCGTCCGCAGCGGCGTGAGGGGGGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGAG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr2:39437092..39437312;chr2:39436986..39437246 26863196 MeRIP-seq:(Medium) rs1402931465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777799,Human_RBP_ID_9330990,Human_RBP_ID_9386395,Human_RBP_ID_18421746,Human_RBP_ID_22077036,Human_RBP_ID_22597969,Human_RBP_ID_22997134,Human_RBP_ID_26770142,Human_RBP_ID_27817027 74868 RMVar_ID_74868 Human_SNP_ID_68133727 m1A Human chr2 + 39453845 39453845 39453845 ATTTTATTTATTTATTTTTTTTATAGAGGCAGAGTCTTGCTTTGTTGTCCAGGCTGGTCTTGAAC ATTTTATTTATTTATTTTTTTTATAGAGGCAGGGTCTTGCTTTGTTGTCCAGGCTGGTCTTGAAC A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78716897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625806 Human_Splice_Rec_238268,Human_Splice_Rec_238269,Human_Splice_Rec_238278,Human_Splice_Rec_238279,Human_Splice_Rec_238294,Human_Splice_Rec_238295,Human_Splice_Rec_238306,Human_Splice_Rec_238307,Human_Splice_Rec_238318,Human_Splice_Rec_238319,Human_Splice_Rec_238332,Human_Splice_Rec_238333,Human_Splice_Rec_238346,Human_Splice_Rec_238347,Human_Splice_Rec_238358,Human_Splice_Rec_238359,Human_Splice_Rec_238364,Human_Splice_Rec_238365,Human_Splice_Rec_238376,Human_Splice_Rec_238377,Human_Splice_Rec_238388,Human_Splice_Rec_238389,Human_Splice_Rec_238398,Human_Splice_Rec_238399,Human_Splice_Rec_238408,Human_Splice_Rec_238409,Human_Splice_Rec_238422,Human_Splice_Rec_238423,Human_Splice_Rec_238433,Human_Splice_Rec_238435 RMVar_hsa_circ_121523,RMVar_hsa_circ_199185 74869 RMVar_ID_74869 Human_SNP_ID_68331522 m1A Human chr2 - 40112846 40112846 40112846 GTTTGGAAAACCACCCTCTTTATCTTTGACCGACTTGCAGATAAATATATCTCTCCATTTTAAAC GTTTGGAAAACCACCCTCTTTATCTTTGACCGGCTTGCAGATAAATATATCTCTCCATTTTAAAC T C SLC8A1 Ensembl:ENSG00000183023 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs5551 Functional Loss SNV dbSNP153 33..33 33 - - - 74870 RMVar_ID_74870 Human_SNP_ID_68846567 m1A Human chr2 - 41769962 41769962 41769962 TGGTGGATGGAAGCAGAGTTGCTGATGTGGGGACAAGGGTGAGGATGAATGGAAAGGGCGTCTTA TGGTGGATGGAAGCAGAGTTGCTGATGTGGGGGCAAGGGTGAGGATGAATGGAAAGGGCGTCTTA T C LINC01914,LINC01914:2,LINC01914:3 RNACentral:URS0000D5B424,RNACentral:URS0000D570CB,RNACentral:URS0000D5B65A lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:41769915..41770028 26863196 MeRIP-seq:(Medium) rs1179535480 Functional Loss SNV dbSNP153 33..33 33 - - - 74871 RMVar_ID_74871 Human_SNP_ID_68932655 m1A Human chr2 - 42047596 42047596 42047596 GGATAACGGAGCCGGCCGGGCGGAGTGGGGGAAAGATAAAGGGGCGAGGCCGGCGGGTAGCGGGC GGATAACGGAGCCGGCCGGGCGGAGTGGGGGACAGATAAAGGGGCGAGGCCGGCGGGTAGCGGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:42047550..42047653;chr2:42047545..42047662 26863196 MeRIP-seq:(Medium) rs1349654077 Functional Loss SNV dbSNP153 33..33 33 - - - 74872 RMVar_ID_74872 Human_SNP_ID_68932974 m1A Human chr2 + 42048080 42048080 42048080 CGCGAGGGGCCGGGGTCGGGGCCGCCGGGGCCATGCGCGCGGGCTGGGCAGGGGGCCGGCGGGGC CGCGAGGGGCCGGGGTCGGGGCCGCCGGGGCCGTGCGCGCGGGCTGGGCAGGGGGCCGGCGGGGC A G PKDCC Ensembl:ENSG00000162878 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:42048001..42048849;chr2:42048026..42048650;chr2:42048026..42048425;chr2:42048001..42048865;chr2:42048001..42048860;chr2:42048026..42048867;chr2:42048026..42048225 26863196 MeRIP-seq:(Medium) rs1258325190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243830,Human_RBP_ID_18421750,Human_RBP_ID_18462498,Human_RBP_ID_26786889 74873 RMVar_ID_74873 Human_SNP_ID_68932979 m1A Human chr2 - 42048092 42048092 42048092 GCTCCGCTCTGCGCCCCGCCGGCCCCCTGCCCAGCCCGCGCGCATGGCCCCGGCGGCCCCGACCC GCTCCGCTCTGCGCCCCGCCGGCCCCCTGCCCGGCCCGCGCGCATGGCCCCGGCGGCCCCGACCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:42048046..42048195 26863196 MeRIP-seq:(Medium) rs1217325669 Functional Loss SNV dbSNP153 33..33 33 - - - 74874 RMVar_ID_74874 Human_SNP_ID_68932980 m1A Human chr2 - 42048092 42048092 42048092 GCTCCGCTCTGCGCCCCGCCGGCCCCCTGCCCAGCCCGCGCGCATGGCCCCGGCGGCCCCGACCC GCTCCGCTCTGCGCCCCGCCGGCCCCCTGCCCCGCCCGCGCGCATGGCCCCGGCGGCCCCGACCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:42048046..42048195 26863196 MeRIP-seq:(Medium) rs1217325669 Functional Loss SNV dbSNP153 33..33 33 - - - 74875 RMVar_ID_74875 Human_SNP_ID_68932995 m1A Human chr2 + 42048122 42048122 42048122 GCTGGGCAGGGGGCCGGCGGGGCGCAGAGCGGAGCCGCCTCGGAGCCTGAGCCGCCCGGGGCCGG GCTGGGCAGGGGGCCGGCGGGGCGCAGAGCGGCGCCGCCTCGGAGCCTGAGCCGCCCGGGGCCGG A C PKDCC Ensembl:ENSG00000162878 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:42048025..42048169 26863410 MeRIP-seq:(Medium) rs1261630837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421750,Human_RBP_ID_18462498,Human_RBP_ID_26786889 74876 RMVar_ID_74876 Human_SNP_ID_68933014 m1A Human chr2 + 42048163 42048157 42048163 GGAGCCTGAGCCGCCCGGGGCCGGGGCCGGGGAGCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG GGAGCCTGAGCCGCCCGGGGCCGGGGC______GCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG CCGGGGA C PKDCC Ensembl:ENSG00000162878 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:42048069..42048268 26863410 MeRIP-seq:(Medium) rs1190834833 Functional Loss DEL dbSNP153 28..33 33 - - - 74877 RMVar_ID_74877 Human_SNP_ID_68933018 m1A Human chr2 + 42048163 42048163 42048163 GGAGCCTGAGCCGCCCGGGGCCGGGGCCGGGGAGCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG GGAGCCTGAGCCGCCCGGGGCCGGGGCCGGGGCGCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG A C PKDCC Ensembl:ENSG00000162878 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:42048069..42048268 26863410 MeRIP-seq:(Medium) rs866273859 Functional Loss SNV dbSNP153 33..33 33 - - - 74878 RMVar_ID_74878 Human_SNP_ID_68933019 m1A Human chr2 + 42048163 42048163 42048163 GGAGCCTGAGCCGCCCGGGGCCGGGGCCGGGGAGCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG GGAGCCTGAGCCGCCCGGGGCCGGGGCCGGGGGGCCGCGCGGGGCCGGCCGGCCGGGGGGAGGGG A G PKDCC Ensembl:ENSG00000162878 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:42048069..42048268 26863410 MeRIP-seq:(Medium) rs866273859 Functional Loss SNV dbSNP153 33..33 33 - - - 74879 RMVar_ID_74879 Human_SNP_ID_68935084 m1A Human chr2 - 42054364 42054364 42054364 CAGCTGGCCTCCACGTTGGCTCTCTTCCTGCCATGCCCTCCTGGCCCATTCTCCTTCGATGGAGT CAGCTGGCCTCCACGTTGGCTCTCTTCCTGCCGTGCCCTCCTGGCCCATTCTCCTTCGATGGAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:42054351..42054516 26863196 MeRIP-seq:(Medium) rs971517339 Functional Loss SNV dbSNP153 33..33 33 - - - 74880 RMVar_ID_74880 Human_SNP_ID_68979117 m1A Human chr2 + 42199024 42199024 42199024 AGAGTGGTTGAAGTTATGTATCTTGGGGGTTTAGGCTGGAGAGGGAACACCTTGAAGCCAAGACA AGAGTGGTTGAAGTTATGTATCTTGGGGGTTTGGGCTGGAGAGGGAACACCTTGAAGCCAAGACA A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:42199023..42199135 26863196 MeRIP-seq:(Medium) rs1204921820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827039,Human_RBP_ID_17139852,Human_RBP_ID_24376419 RMVar_hsa_circ_117094,RMVar_hsa_circ_199225 74881 RMVar_ID_74881 Human_SNP_ID_69021703 m1A Human chr2 + 42329996 42329996 42329996 TCCTTCTCAGCCCTTAAATGAGACAGCTGAAGAGGAAAGTAGAATAAGCAGTTCTCCCACACTTC TCCTTCTCAGCCCTTAAATGAGACAGCTGAAGGGGAAAGTAGAATAAGCAGTTCTCCCACACTTC A G EML4 Ensembl:ENSG00000143924 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:42329945..42330185 26863196 MeRIP-seq:(Medium) rs753093955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5589394,Human_RBP_ID_13888415,Human_RBP_ID_22078032 Human_miRNA_ID_316023,Human_miRNA_ID_319296 74882 RMVar_ID_74882 Human_SNP_ID_69029862 m1A Human chr2 + 42357640 42357640 42357640 GACCTCTATTTATTTCTAACGGTAAGCTAGACATCACCACCTACCTCCATGTCCTTCTGACACCT GACCTCTATTTATTTCTAACGGTAAGCTAGACTTCACCACCTACCTCCATGTCCTTCTGACACCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:42357637..42357721 26863196 MeRIP-seq:(Medium) rs1225571794 Functional Loss SNV dbSNP153 33..33 33 - - - 74883 RMVar_ID_74883 Human_SNP_ID_69029891 m1A Human chr2 - 42357786 42357786 42357786 GAGTTGTGGTAGTTTGTCCTTTCAGATGAGACAGATGTTGGGGATGAGGAGGGAGGGCTTCAGCA GAGTTGTGGTAGTTTGTCCTTTCAGATGAGACGGATGTTGGGGATGAGGAGGGAGGGCTTCAGCA T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:42357784..42357945;chr2:42357784..42358013 26863196 MeRIP-seq:(Medium) rs960738146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23872161 74884 RMVar_ID_74884 Human_SNP_ID_69030446 m1A Human chr2 - 42359692 42359692 42359692 TGGGTGTCTTCAGCCCATAGGTGGTAATTTGTAGGGAAGAAAGGTTGGATTATAGTTAGAGTATA TGGGTGTCTTCAGCCCATAGGTGGTAATTTGTGGGGAAGAAAGGTTGGATTATAGTTAGAGTATA T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:42359690..42359805 26863196 MeRIP-seq:(Medium) rs557258581 Functional Loss SNV dbSNP153 33..33 33 - - - 74885 RMVar_ID_74885 Human_SNP_ID_69030447 m1A Human chr2 - 42359692 42359692 42359692 TGGGTGTCTTCAGCCCATAGGTGGTAATTTGTAGGGAAGAAAGGTTGGATTATAGTTAGAGTATA TGGGTGTCTTCAGCCCATAGGTGGTAATTTGTCGGGAAGAAAGGTTGGATTATAGTTAGAGTATA T G COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:42359690..42359805 26863196 MeRIP-seq:(Medium) rs557258581 Functional Loss SNV dbSNP153 33..33 33 - - - 74886 RMVar_ID_74886 Human_SNP_ID_69030972 m1A Human chr2 - 42361133 42361133 42361133 CGTCATGTACTACAAGTTTAGTGGCTTCACGCAGAAGTTGGCAGGAGCATGGGCTTCGGAGGCCT CGTCATGTACTACAAGTTTAGTGGCTTCACGCGGAAGTTGGCAGGAGCATGGGCTTCGGAGGCCT T C COX7A2L Ensembl:ENSG00000115944 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs973677002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280908,Human_RBP_ID_551071,Human_RBP_ID_4623259,Human_RBP_ID_5146532,Human_RBP_ID_8234313,Human_RBP_ID_9106624,Human_RBP_ID_13889055,Human_RBP_ID_22451229,Human_RBP_ID_23872172,Human_RBP_ID_26819690 Human_Splice_Rec_239345,Human_Splice_Rec_239349,Human_Splice_Rec_239355,Human_Splice_Rec_239371 74887 RMVar_ID_74887 Human_SNP_ID_69031009 m1A Human chr2 + 42361171 42361171 42361171 AAGCCACTAAACTTGTAGTACATGACGCCCAGAGTCCGGCTTCCCGCATCCGCTGCCAACGCGAC AAGCCACTAAACTTGTAGTACATGACGCCCAGGGTCCGGCTTCCCGCATCCGCTGCCAACGCGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:42361047..42361225 26863196 MeRIP-seq:(Medium) rs768755431 Functional Loss SNV dbSNP153 33..33 33 - - - 74888 RMVar_ID_74888 Human_SNP_ID_69031010 m1A Human chr2 + 42361171 42361171 42361171 AAGCCACTAAACTTGTAGTACATGACGCCCAGAGTCCGGCTTCCCGCATCCGCTGCCAACGCGAC AAGCCACTAAACTTGTAGTACATGACGCCCAGTGTCCGGCTTCCCGCATCCGCTGCCAACGCGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:42361047..42361225 26863196 MeRIP-seq:(Medium) rs768755431 Functional Loss SNV dbSNP153 33..33 33 - - - 74889 RMVar_ID_74889 Human_SNP_ID_69031013 m1A Human chr2 - 42361173 42361173 42361173 CGGTCGCGTTGGCAGCGGATGCGGGAAGCCGGACTCTGGGCGTCATGTACTACAAGTTTAGTGGC CGGTCGCGTTGGCAGCGGATGCGGGAAGCCGGTCTCTGGGCGTCATGTACTACAAGTTTAGTGGC T A COX7A2L Ensembl:ENSG00000115944 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:42361126..42361200 26863196 MeRIP-seq:(Medium) rs748436653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243525,Human_RBP_ID_551072,Human_RBP_ID_776858,Human_RBP_ID_1586945,Human_RBP_ID_4623260,Human_RBP_ID_5146532,Human_RBP_ID_6920937,Human_RBP_ID_9330991,Human_RBP_ID_13889060,Human_RBP_ID_17658048,Human_RBP_ID_22449784 Human_Splice_Rec_239345,Human_Splice_Rec_239349,Human_Splice_Rec_239355,Human_Splice_Rec_239371 74890 RMVar_ID_74890 Human_SNP_ID_69031023 m1A Human chr2 - 42361179 42361179 42361179 CTGGGGCGGTCGCGTTGGCAGCGGATGCGGGAAGCCGGACTCTGGGCGTCATGTACTACAAGTTT CTGGGGCGGTCGCGTTGGCAGCGGATGCGGGACGCCGGACTCTGGGCGTCATGTACTACAAGTTT T G COX7A2L Ensembl:ENSG00000115944 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:42361033..42361182 26863196 MeRIP-seq:(Medium) rs894199803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243525,Human_RBP_ID_551072,Human_RBP_ID_776858,Human_RBP_ID_1586945,Human_RBP_ID_4623260,Human_RBP_ID_5146532,Human_RBP_ID_6920937,Human_RBP_ID_9330991,Human_RBP_ID_13889060,Human_RBP_ID_17658048,Human_RBP_ID_22449784 Human_Splice_Rec_239345,Human_Splice_Rec_239349,Human_Splice_Rec_239355,Human_Splice_Rec_239371 74891 RMVar_ID_74891 Human_SNP_ID_69070561 m1A Human chr2 + 42493598 42493598 42493598 CGCGGGGCCTGCCTGCCCGTGGCTGACGGGGGAGCGCGCCGTCGGGGCCCGCGCTCCCTCGGGGC CGCGGGGCCTGCCTGCCCGTGGCTGACGGGGGGGCGCGCCGTCGGGGCCCGCGCTCCCTCGGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:42493548..42493662 26863196 MeRIP-seq:(Medium) rs1323940799 Functional Loss SNV dbSNP153 33..33 33 - - - 74892 RMVar_ID_74892 Human_SNP_ID_69135605 m1A Human chr2 + 42700082 42700082 42700082 TAACAGTGTTGGATGCTGGTGGGAAATAGCCAAGTAATTTAATAACATGGAGATCATTGGTGATC TAACAGTGTTGGATGCTGGTGGGAAATAGCCAGGTAATTTAATAACATGGAGATCATTGGTGATC A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:42700056..42700197 26863196 MeRIP-seq:(Medium) rs1319845649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5195062 RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_49197,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_199269,RMVar_hsa_circ_366146,RMVar_hsa_circ_108363,RMVar_hsa_circ_99859,RMVar_hsa_circ_199275,RMVar_hsa_circ_97193,RMVar_hsa_circ_56390,RMVar_hsa_circ_126540,RMVar_hsa_circ_199276,RMVar_hsa_circ_80564,RMVar_hsa_circ_104079,RMVar_hsa_circ_199277,RMVar_hsa_circ_199278,RMVar_hsa_circ_113659,RMVar_hsa_circ_277908,RMVar_hsa_circ_199280,RMVar_hsa_circ_199281,RMVar_hsa_circ_310166,RMVar_hsa_circ_317676,RMVar_hsa_circ_122339,RMVar_hsa_circ_199284,RMVar_hsa_circ_199286,RMVar_hsa_circ_199287,RMVar_hsa_circ_199285,RMVar_hsa_circ_199289,RMVar_hsa_circ_280290,RMVar_hsa_circ_299140,RMVar_hsa_circ_366226,RMVar_hsa_circ_308536,RMVar_hsa_circ_84387,RMVar_hsa_circ_103739,RMVar_hsa_circ_199291,RMVar_hsa_circ_199290,RMVar_hsa_circ_126295,RMVar_hsa_circ_199288,RMVar_hsa_circ_369941,RMVar_hsa_circ_199294,RMVar_hsa_circ_41271,RMVar_hsa_circ_199293 74893 RMVar_ID_74893 Human_SNP_ID_69168209 m1A Human chr2 + 42810587 42810587 42810587 TTAGCGCGCGGTACTTATACAGCAGTACATGCAGAGCAATGCCGAGGTTGTGAGTTCGAGCCTCA TTAGCGCGCGGTACTTATACAGCAGTACATGCGGAGCAATGCCGAGGTTGTGAGTTCGAGCCTCA A G lnc-MTA3-5,lnc-MTA3-6,TRI-TAT2-1,tRNA-Ile-TAT-2-1 RNACentral:URS00009B1B7A,RNACentral:URS00008BFDCC,RNACentral:URS00004E1F23,RNACentral:URS00007362AD lincRNA,lincRNA,tRNA,tRNA intron,exon,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:42810549..42810617 26863196 MeRIP-seq:(Medium) rs1287035334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1023296,Human_RBP_ID_1196120,Human_RBP_ID_1301167,Human_RBP_ID_1378273,Human_RBP_ID_1592877,Human_RBP_ID_1917892,Human_RBP_ID_3626200,Human_RBP_ID_4632857,Human_RBP_ID_5249519,Human_RBP_ID_6921522,Human_RBP_ID_8257631,Human_RBP_ID_8519075,Human_RBP_ID_8848288,Human_RBP_ID_9106659,Human_RBP_ID_13889756,Human_RBP_ID_17587199,Human_RBP_ID_18209055,Human_RBP_ID_18760937,Human_RBP_ID_20573063,Human_RBP_ID_22815596,Human_RBP_ID_23133021,Human_RBP_ID_23872436,Human_RBP_ID_24423885,Human_RBP_ID_24489398,Human_RBP_ID_26666252,Human_RBP_ID_27011854,Human_RBP_ID_27480140,Human_RBP_ID_27563871,Human_RBP_ID_27696105 74894 RMVar_ID_74894 Human_SNP_ID_69168212 m1A Human chr2 + 42810589 42810589 42810589 AGCGCGCGGTACTTATACAGCAGTACATGCAGAGCAATGCCGAGGTTGTGAGTTCGAGCCTCACC AGCGCGCGGTACTTATACAGCAGTACATGCAGGGCAATGCCGAGGTTGTGAGTTCGAGCCTCACC A G lnc-MTA3-5,lnc-MTA3-6,TRI-TAT2-1,tRNA-Ile-TAT-2-1 RNACentral:URS00009B1B7A,RNACentral:URS00008BFDCC,RNACentral:URS00004E1F23,RNACentral:URS00007362AD lincRNA,lincRNA,tRNA,tRNA intron,exon,exon,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:42810507..42810672;chr2:42810503..42810676 26863196 MeRIP-seq:(Medium) rs1355556159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1023296,Human_RBP_ID_1196120,Human_RBP_ID_1301167,Human_RBP_ID_1378273,Human_RBP_ID_1592877,Human_RBP_ID_1917892,Human_RBP_ID_3626200,Human_RBP_ID_4632857,Human_RBP_ID_6921522,Human_RBP_ID_8257631,Human_RBP_ID_8519075,Human_RBP_ID_8848288,Human_RBP_ID_9106659,Human_RBP_ID_13889756,Human_RBP_ID_17587199,Human_RBP_ID_18209055,Human_RBP_ID_18760937,Human_RBP_ID_20573063,Human_RBP_ID_22815596,Human_RBP_ID_23133021,Human_RBP_ID_23872436,Human_RBP_ID_24423885,Human_RBP_ID_24489398,Human_RBP_ID_26487760,Human_RBP_ID_26666252,Human_RBP_ID_27011854,Human_RBP_ID_27480140,Human_RBP_ID_27563871,Human_RBP_ID_27696105 74895 RMVar_ID_74895 Human_SNP_ID_69168228 m1A Human chr2 + 42810599 42810599 42810599 ACTTATACAGCAGTACATGCAGAGCAATGCCGAGGTTGTGAGTTCGAGCCTCACCTGGAGCAAGA ACTTATACAGCAGTACATGCAGAGCAATGCCGCGGTTGTGAGTTCGAGCCTCACCTGGAGCAAGA A C lnc-MTA3-5,lnc-MTA3-6,TRI-TAT2-1,tRNA-Ile-TAT-2-1 RNACentral:URS00009B1B7A,RNACentral:URS00008BFDCC,RNACentral:URS00004E1F23,RNACentral:URS00007362AD lincRNA,lincRNA,tRNA,tRNA intron,exon,exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:42810506..42810674;chr2:42810502..42810676 26863196 MeRIP-seq:(Medium) rs1255801250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_551132,Human_RBP_ID_1023296,Human_RBP_ID_1196120,Human_RBP_ID_1378273,Human_RBP_ID_1592877,Human_RBP_ID_1917892,Human_RBP_ID_3626200,Human_RBP_ID_4632857,Human_RBP_ID_6921522,Human_RBP_ID_8257631,Human_RBP_ID_8519075,Human_RBP_ID_8848289,Human_RBP_ID_9106659,Human_RBP_ID_13889756,Human_RBP_ID_17394471,Human_RBP_ID_18209055,Human_RBP_ID_18760937,Human_RBP_ID_20573063,Human_RBP_ID_22815596,Human_RBP_ID_23133021,Human_RBP_ID_23872436,Human_RBP_ID_24489398,Human_RBP_ID_26666252,Human_RBP_ID_27011854,Human_RBP_ID_27480140,Human_RBP_ID_27563871,Human_RBP_ID_27696105 74896 RMVar_ID_74896 Human_SNP_ID_69168238 m1A Human chr2 + 42810613 42810613 42810613 ACATGCAGAGCAATGCCGAGGTTGTGAGTTCGAGCCTCACCTGGAGCAAGACCCTTTTGGATGTT ACATGCAGAGCAATGCCGAGGTTGTGAGTTCGCGCCTCACCTGGAGCAAGACCCTTTTGGATGTT A C lnc-HAAO-1,lnc-HAAO-1:2 RNACentral:URS00008B3DA3,RNACentral:URS00008BB89F lincRNA,lincRNA intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs916140517 Functional Loss SNV dbSNP153 33..33 33 - - - 74897 RMVar_ID_74897 Human_SNP_ID_69293629 m1A Human chr2 - 43224312 43224312 43224312 GCCGCCTCTCCATCTCCGACGACTGAGGCAAGAGGGCGCCAGTGAGGAGGAAGGGAAGGCGGTTC GCCGCCTCTCCATCTCCGACGACTGAGGCAAGCGGGCGCCAGTGAGGAGGAAGGGAAGGCGGTTC T G ZFP36L2 Ensembl:ENSG00000152518 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:43224276..43224375 26863196 MeRIP-seq:(Medium) rs757323833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776262,Human_RBP_ID_829929,Human_RBP_ID_5146799,Human_RBP_ID_6921605,Human_RBP_ID_13889858,Human_RBP_ID_17509632,Human_RBP_ID_22078041 RMVar_hsa_circ_199307,RMVar_hsa_circ_89941 74898 RMVar_ID_74898 Human_SNP_ID_69293672 m1A Human chr2 - 43224396 43224396 43224396 ACCTAAGCGGCTCCCTGAGCTCCGGCAGCCTCAGCGGCTCTGAGTCTCCCAGCCTCGACCCTGGC ACCTAAGCGGCTCCCTGAGCTCCGGCAGCCTCGGCGGCTCTGAGTCTCCCAGCCTCGACCCTGGC T C ZFP36L2 Ensembl:ENSG00000152518 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:43224346..43224650 26863196 MeRIP-seq:(Medium) rs929758325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1023310,Human_RBP_ID_6921609,Human_RBP_ID_8848295,Human_RBP_ID_18470786 Human_miRNA_ID_2712514,Human_miRNA_ID_3048496 RMVar_hsa_circ_199307,RMVar_hsa_circ_89941 74899 RMVar_ID_74899 Human_SNP_ID_69293775 m1A Human chr2 + 43224554 43224554 43224554 GCGGCGAGGGAGGTGCGGCGGCCCCGGCGGGGAGGGTCGCGCTGGGCGGCGCCGGCGGCTGCGCG GCGGCGAGGGAGGTGCGGCGGCCCCGGCGGGGGGGGTCGCGCTGGGCGGCGCCGGCGGCTGCGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:43224351..43225000 26863410 MeRIP-seq:(Medium) rs987176799 Functional Loss SNV dbSNP153 33..33 33 - - - 74900 RMVar_ID_74900 Human_SNP_ID_69293778 m1A Human chr2 - 43224558 43224558 43224558 CCCCCGCGCAGCCGCCGGCGCCGCCCAGCGCGACCCTCCCCGCCGGGGCCGCCGCACCTCCCTCG CCCCCGCGCAGCCGCCGGCGCCGCCCAGCGCGCCCCTCCCCGCCGGGGCCGCCGCACCTCCCTCG T G ZFP36L2 Ensembl:ENSG00000152518 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:43224451..43224749 26863410 MeRIP-seq:(Medium) rs1017664195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2146007,Human_miRNA_ID_2987442,Human_miRNA_ID_3021133 RMVar_hsa_circ_199307,RMVar_hsa_circ_89941 74901 RMVar_ID_74901 Human_SNP_ID_69294070 m1A Human chr2 + 43224912 43224874 43224913 CGAGGAACAGGAGGAGGCGGAGGAGGAGCAGGACGAGGCCGAAGAGCAGGAGGGCGGCGGCGGCG __________________________________GAGGCCGAAGAGCAGGAGGGCGGCGGCGGCG GGAGGCCGAGGAACAGGAGGAGGCGGAGGAGGAGCAGGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:43224862..43224980 26863196 MeRIP-seq:(Medium) rs1273957053 Functional Loss DEL dbSNP153 1..34 33 - - - 74902 RMVar_ID_74902 Human_SNP_ID_69294151 m1A Human chr2 + 43224971 43224971 43224971 GCGGCGTGCGCGACGTGGGGCTGTCGAGCAGCAGCGGCGACTCGAGGCCGCCCGGGGGCTGATGG GCGGCGTGCGCGACGTGGGGCTGTCGAGCAGCCGCGGCGACTCGAGGCCGCCCGGGGGCTGATGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:43224876..43225000 26863196 MeRIP-seq:(Medium) rs1423163686 Functional Loss SNV dbSNP153 33..33 33 - - - 74903 RMVar_ID_74903 Human_SNP_ID_69294152 m1A Human chr2 + 43224971 43224971 43224971 GCGGCGTGCGCGACGTGGGGCTGTCGAGCAGCAGCGGCGACTCGAGGCCGCCCGGGGGCTGATGG GCGGCGTGCGCGACGTGGGGCTGTCGAGCAGCTGCGGCGACTCGAGGCCGCCCGGGGGCTGATGG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:43224876..43225000 26863196 MeRIP-seq:(Medium) rs1423163686 Functional Loss SNV dbSNP153 33..33 33 - - - 74904 RMVar_ID_74904 Human_SNP_ID_69295113 m1A Human chr2 + 43226455 43226455 43226455 GAGGGGCCGAAAGTTTGCCGGGGGGCGAGAGGAGAGGGCGAGTGCAGCGGCGCGGGCCGGCGGGA GAGGGGCCGAAAGTTTGCCGGGGGGCGAGAGGTGAGGGCGAGTGCAGCGGCGCGGGCCGGCGGGA A T - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr2:43226358..43226459 26863410 MeRIP-seq:(Medium) rs1461973799 Functional Loss SNV dbSNP153 33..33 33 - - - 74905 RMVar_ID_74905 Human_SNP_ID_69526907 m1A Human chr2 + 43995889 43995889 43995889 GGCCGCCAGGGAGGAGGCGCAGGGAGAGCGGGAGGCGCGGGGCCGCCCCGGCACGCAGCAACCAA GGCCGCCAGGGAGGAGGCGCAGGGAGAGCGGGCGGCGCGGGGCCGCCCCGGCACGCAGCAACCAA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:43995776..43995975 26863410 MeRIP-seq:(Medium) rs1469447759 Functional Loss SNV dbSNP153 33..33 33 - - - 74906 RMVar_ID_74906 Human_SNP_ID_69526941 m1A Human chr2 + 43995929 43995929 43995929 GGCCGCCCCGGCACGCAGCAACCAACGCGCGGATCTCAGCAGGGCTGCCATTGCTCGAACGTCCC GGCCGCCCCGGCACGCAGCAACCAACGCGCGGGTCTCAGCAGGGCTGCCATTGCTCGAACGTCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:43995776..43996000 26863196 MeRIP-seq:(Medium) rs1285024042 Functional Loss SNV dbSNP153 33..33 33 - - - 74907 RMVar_ID_74907 Human_SNP_ID_69526948 m1A Human chr2 + 43995937 43995937 43995937 CGGCACGCAGCAACCAACGCGCGGATCTCAGCAGGGCTGCCATTGCTCGAACGTCCCCGCAGCGG CGGCACGCAGCAACCAACGCGCGGATCTCAGCTGGGCTGCCATTGCTCGAACGTCCCCGCAGCGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:43995776..43996000;chr2:43995826..43995975 26863196 MeRIP-seq:(Medium) rs1284924066 Functional Loss SNV dbSNP153 33..33 33 - - - 74908 RMVar_ID_74908 Human_SNP_ID_69526969 m1A Human chr2 - 43995951 43995951 43995951 GCGGAGCGTGCTTCCCGCTGCGGGGACGTTCGAGCAATGGCAGCCCTGCTGAGATCCGCGCGTTG GCGGAGCGTGCTTCCCGCTGCGGGGACGTTCGGGCAATGGCAGCCCTGCTGAGATCCGCGCGTTG T C LRPPRC Ensembl:ENSG00000138095 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr2:43995901..43995975;chr2:43995901..43995950 26863196 MeRIP-seq:(Medium) rs1559083136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59107,Human_RBP_ID_551330,Human_RBP_ID_828415,Human_RBP_ID_4622366,Human_RBP_ID_8851172,Human_RBP_ID_9259708,Human_RBP_ID_9296450,Human_RBP_ID_9330436,Human_RBP_ID_18193285,Human_RBP_ID_18421756,Human_RBP_ID_23873049 Human_miRNA_ID_2219687,Human_miRNA_ID_2482726,Human_miRNA_ID_3071100 RMVar_hsa_circ_126864,RMVar_hsa_circ_199446,RMVar_hsa_circ_122331,RMVar_hsa_circ_199465 74909 RMVar_ID_74909 Human_SNP_ID_69584804 m1A Human chr2 + 44169060 44169060 44169060 CGAGGCTGCGGCGGAGGAGGTGGCGGCGGCCGAATCGGCAACGGCGCTAGGGTGGAGAGAAGGCG CGAGGCTGCGGCGGAGGAGGTGGCGGCGGCCGCATCGGCAACGGCGCTAGGGTGGAGAGAAGGCG A C PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:44168901..44169275 26863196 MeRIP-seq:(Medium) rs1338859612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622368,Human_RBP_ID_8851834,Human_RBP_ID_8942568,Human_RBP_ID_9330438 RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 74910 RMVar_ID_74910 Human_SNP_ID_69584814 m1A Human chr2 + 44169083 44169081 44169083 CGGCGGCCGAATCGGCAACGGCGCTAGGGTGGAGAGAAGGCGGCATCGGCGGCGGCGGCGGCGTG CGGCGGCCGAATCGGCAACGGCGCTAGGGTG__GAGAAGGCGGCATCGGCGGCGGCGGCGGCGTG GGA G PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:44168923..44169275;chr2:44168873..44169275 26863196 MeRIP-seq:(Medium) rs1165527852 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_920472,Human_RBP_ID_4610018,Human_RBP_ID_8851834,Human_RBP_ID_8942568,Human_RBP_ID_9330438 Human_miRNA_ID_3115896 RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 74911 RMVar_ID_74911 Human_SNP_ID_69584815 m1A Human chr2 + 44169083 44169083 44169083 CGGCGGCCGAATCGGCAACGGCGCTAGGGTGGAGAGAAGGCGGCATCGGCGGCGGCGGCGGCGTG CGGCGGCCGAATCGGCAACGGCGCTAGGGTGGTGAGAAGGCGGCATCGGCGGCGGCGGCGGCGTG A T PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:44168923..44169275;chr2:44168873..44169275 26863196 MeRIP-seq:(Medium) rs981401495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920472,Human_RBP_ID_4610018,Human_RBP_ID_8851834,Human_RBP_ID_8942568,Human_RBP_ID_9330438 Human_miRNA_ID_3115896 RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 74912 RMVar_ID_74912 Human_SNP_ID_69584818 m1A Human chr2 - 44169096 44169088 44169097 CCGCCCGGCCCCTCACGCCGCCGCCGCCGCCGATGCCGCCTTCTCTCCACCCTAGCGCCGTTGCC CCGCCCGGCCCCTCACGCCGCCGCCGCCGCC_________TTCTCTCCACCCTAGCGCCGTTGCC AGGCGGCATC A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:44168986..44169233 26863196 MeRIP-seq:(Medium) rs1475828427 Functional Loss DEL dbSNP153 32..40 33 - - - 74913 RMVar_ID_74913 Human_SNP_ID_69584821 m1A Human chr2 - 44169096 44169093 44169096 CCGCCCGGCCCCTCACGCCGCCGCCGCCGCCGATGCCGCCTTCTCTCCACCCTAGCGCCGTTGCC CCGCCCGGCCCCTCACGCCGCCGCCGCCGCCG___CCGCCTTCTCTCCACCCTAGCGCCGTTGCC GCAT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:44168986..44169233 26863196 MeRIP-seq:(Medium) rs1451564944 Functional Loss DEL dbSNP153 33..35 33 - - - 74914 RMVar_ID_74914 Human_SNP_ID_69584826 m1A Human chr2 - 44169096 44169096 44169096 CCGCCCGGCCCCTCACGCCGCCGCCGCCGCCGATGCCGCCTTCTCTCCACCCTAGCGCCGTTGCC CCGCCCGGCCCCTCACGCCGCCGCCGCCGCCGCTGCCGCCTTCTCTCCACCCTAGCGCCGTTGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:44168986..44169233 26863196 MeRIP-seq:(Medium) rs12712912 Functional Loss SNV dbSNP153 33..33 33 - - - 74915 RMVar_ID_74915 Human_SNP_ID_69600515 m1A Human chr2 + 44216964 44216964 44216964 AGAGGGGTTGGATTAGAGTGAAAAGTGTTCCCAAACCAACGAAAAGAGTATGTGAAGATCTAGAA AGAGGGGTTGGATTAGAGTGAAAAGTGTTCCCCAACCAACGAAAAGAGTATGTGAAGATCTAGAA A C PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:44216960..44217114 26863196 MeRIP-seq:(Medium) rs910326342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92064,RMVar_hsa_circ_199468,RMVar_hsa_circ_280866,RMVar_hsa_circ_199471,RMVar_hsa_circ_199475,RMVar_hsa_circ_270244,RMVar_hsa_circ_268463,RMVar_hsa_circ_199474,RMVar_hsa_circ_355968 74916 RMVar_ID_74916 Human_SNP_ID_69634443 m1A Human chr2 - 44319602 44319602 44319602 ACTTTTTTTTACCATAATAGTATGTGTTCATTAAAGATGATTTGGGTTTATTTTACAGCTATATA ACTTTTTTTTACCATAATAGTATGTGTTCATTGAAGATGATTTGGGTTTATTTTACAGCTATATA T C PREPL Ensembl:ENSG00000138078 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1056865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3626763,Human_RBP_ID_9106851,Human_RBP_ID_18180913,Human_RBP_ID_18317272,Human_RBP_ID_27696274 GWAS_ID_9069,GWAS_ID_9070,GWAS_ID_9071,GWAS_ID_9072,GWAS_ID_9073 RMVar_hsa_circ_48782,RMVar_hsa_circ_279804,RMVar_hsa_circ_199477 74917 RMVar_ID_74917 Human_SNP_ID_69635915 m1A Human chr2 + 44323405 44323405 44323405 AGTGTCCATCATGGTGTTGAGAACATCCAAGAAAGGTGCCTAAAAAAAAGGCAAAGAAACTTATA AGTGTCCATCATGGTGTTGAGAACATCCAAGACAGGTGCCTAAAAAAAAGGCAAAGAAACTTATA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:44323357..44323441 32194978 MeRIP-seq:(Medium) rs1280968088 Functional Loss SNV dbSNP153 33..33 33 - - - 74918 RMVar_ID_74918 Human_SNP_ID_69648027 m1A Human chr2 + 44361995 44361995 44361995 CGAGCTGCGGCGGTGGCACCTCCGGGTGTGGAAGGCTCCAGTGAGATGGAGTCGCGAGTCGCGGA CGAGCTGCGGCGGTGGCACCTCCGGGTGTGGACGGCTCCAGTGAGATGGAGTCGCGAGTCGCGGA A C CAMKMT Ensembl:ENSG00000143919 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:44361916..44362080 26863196 MeRIP-seq:(Medium) rs1377960190 Functional Loss SNV dbSNP153 33..33 33 - - - 74919 RMVar_ID_74919 Human_SNP_ID_69702278 m1A Human chr2 + 44554292 44554292 44554292 TAGTTAAACATTATGATAGAGGTATGCACTGGATGGTGTGTGAGCACAGAAATCTTCCTAGTAAC TAGTTAAACATTATGATAGAGGTATGCACTGGTTGGTGTGTGAGCACAGAAATCTTCCTAGTAAC A T CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:44554241..44554327 26863196 MeRIP-seq:(Medium) rs1444519929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13899698 RMVar_hsa_circ_199490,RMVar_hsa_circ_199491 74920 RMVar_ID_74920 Human_SNP_ID_69707596 m1A Human chr2 + 44574257 44574257 44574257 TGGGCAAGAGGCAGAACCAGGGAGCATGGCCCAGTGCCTTTATTGGGGTTTTCACAGGATCGAAT TGGGCAAGAGGCAGAACCAGGGAGCATGGCCCGGTGCCTTTATTGGGGTTTTCACAGGATCGAAT A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:44574252..44574363 26863196 MeRIP-seq:(Medium) rs1435989459 Functional Loss SNV dbSNP153 33..33 33 - - - 74921 RMVar_ID_74921 Human_SNP_ID_69752186 m1A Human chr2 + 44745151 44745151 44745151 AAGCATGAAAGTCAGATCAGAGAGCAGCGGCAAAAGGGAAGGGGCAGCATCTTCCTGAAGCTTTA AAGCATGAAAGTCAGATCAGAGAGCAGCGGCAGAAGGGAAGGGGCAGCATCTTCCTGAAGCTTTA A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:44745132..44745271 26863196 MeRIP-seq:(Medium) rs1481259817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4030,RMVar_hsa_circ_70638,RMVar_hsa_circ_378219,RMVar_hsa_circ_54460,RMVar_hsa_circ_29998 74922 RMVar_ID_74922 Human_SNP_ID_69755877 m1A Human chr2 + 44761130 44761130 44761130 GGAGTGGAGGTGGCCAACTGGGGAGGAGGCACAGTAGGGAGGCCAGAGAAGTCAGCAAAGGCGTC GGAGTGGAGGTGGCCAACTGGGGAGGAGGCACTGTAGGGAGGCCAGAGAAGTCAGCAAAGGCGTC A T CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:44761079..44761260 26863196 MeRIP-seq:(Medium) rs1244899412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4030,RMVar_hsa_circ_70638 74923 RMVar_ID_74923 Human_SNP_ID_69802116 m1A Human chr2 - 44935560 44935560 44935560 AGGGCTTAGAGAGCCTGCCCCGGCTTAAGCCGAGCTGCTGGTGCTGACCCTGAGCGCCGAGTCCG AGGGCTTAGAGAGCCTGCCCCGGCTTAAGCCGTGCTGCTGGTGCTGACCCTGAGCGCCGAGTCCG T A LINC01833 Ensembl:ENSG00000259439 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:44935509..44935724 26863196 MeRIP-seq:(Medium) rs1558416694 Functional Loss SNV dbSNP153 33..33 33 - - - 74924 RMVar_ID_74924 Human_SNP_ID_687309837 m1A Human chr21 - 5128342 5128335 5128342 ACCCCGCTGTCCTCACCGCAATGGCGGCTGTGAGGGCCCTGGTGGCCTCGAGGCTCGCTGCGGCA ACCCCGCTGTCCTCACCGCAATGGCGGCTGTG_______TGGTGGCCTCGAGGCTCGCTGCGGCA AGGGCCCT A FP565260.2,GATD3B Ensembl:ENSG00000276612,Ensembl:ENSG00000280071 Protein coding,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:5128266..5128363 26863196 MeRIP-seq:(Medium) rs1422455057 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_4679832,Human_RBP_ID_18423380 74925 RMVar_ID_74925 Human_SNP_ID_687374242 m1A Human chr21 + 6070083 6070080 6070084 TGTGTGTGAAATGTATGTGTGAGGTATGCAGTATGTGTGTGAGGTAGTGTGCGATGTGTGTGTAG TGTGTGTGAAATGTATGTGTGAGGTATGCA____GTGTGTGAGGTAGTGTGCGATGTGTGTGTAG AGTAT A LINC01669 Ensembl:ENSG00000280191 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:6070034..6070118 26863196 MeRIP-seq:(Medium) rs1343293276 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5297512 74926 RMVar_ID_74926 Human_SNP_ID_687374243 m1A Human chr21 + 6070083 6070081 6070083 TGTGTGTGAAATGTATGTGTGAGGTATGCAGTATGTGTGTGAGGTAGTGTGCGATGTGTGTGTAG TGTGTGTGAAATGTATGTGTGAGGTATGCAG__TGTGTGTGAGGTAGTGTGCGATGTGTGTGTAG GTA G LINC01669 Ensembl:ENSG00000280191 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:6070034..6070118 26863196 MeRIP-seq:(Medium) rs1274843695 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5297512 74927 RMVar_ID_74927 Human_SNP_ID_687374244 m1A Human chr21 - 6070086 6070083 6070087 ACACTACACACACATCGCACACTACCTCACACACATACTGCATACCTCACACATACATTTCACAC ACACTACACACACATCGCACACTACCTCACA____TACTGCATACCTCACACATACATTTCACAC ATGTG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:6070035..6070121 26863196 MeRIP-seq:(Medium) rs1224626731 Functional Loss DEL dbSNP153 32..35 33 - - - 74928 RMVar_ID_74928 Human_SNP_ID_687374245 m1A Human chr21 - 6070086 6070083 6070087 ACACTACACACACATCGCACACTACCTCACACACATACTGCATACCTCACACATACATTTCACAC ACACTACACACACATCGCACACTACCTCACA__CATACTGCATACCTCACACATACATTTCACAC ATGTG ATG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:6070035..6070121 26863196 MeRIP-seq:(Medium) rs1224626731 Functional Loss DEL dbSNP153 32..33 33 - - - 74929 RMVar_ID_74929 Human_SNP_ID_687377445 m1A Human chr21 - 6120590 6120590 6120590 GGGCTCAGGCCGCCCCTGCTGGCCCGGCTGGCAGGGACCTGGCACACCTGGCGAGCCAGCCCCTT GGGCTCAGGCCGCCCCTGCTGGCCCGGCTGGCGGGGACCTGGCACACCTGGCGAGCCAGCCCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:6120526..6120632 26863196 MeRIP-seq:(Medium) rs1416981453 Functional Loss SNV dbSNP153 33..33 33 - - - 74930 RMVar_ID_74930 Human_SNP_ID_687388815 m1A Human chr21 + 6499244 6499244 6499244 GACGCCGCCGACCCTGCCGACGCCCGCGGGAGACGTCACCCGGACGCGACGACGCTCTTCCCCGC GACGCCGCCGACCCTGCCGACGCCCGCGGGAGGCGTCACCCGGACGCGACGACGCTCTTCCCCGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:6499148..6499273 26863196 MeRIP-seq:(Medium) rs1159973570 Functional Loss SNV dbSNP153 33..33 33 - - - 74931 RMVar_ID_74931 Human_SNP_ID_687391703 m1A Human chr21 + 6565543 6565543 6565543 CACACACCACACACTCCACACACTCCACACACACCACACACTCCACACTCCACACACTCCACACA CACACACCACACACTCCACACACTCCACACACCCCACACACTCCACACTCCACACACTCCACACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:6565498..6565583 26863196 MeRIP-seq:(Medium) rs1256984789 Functional Loss SNV dbSNP153 33..33 33 - - - 74932 RMVar_ID_74932 Human_SNP_ID_687391704 m1A Human chr21 + 6565543 6565543 6565543 CACACACCACACACTCCACACACTCCACACACACCACACACTCCACACTCCACACACTCCACACA CACACACCACACACTCCACACACTCCACACACTCCACACACTCCACACTCCACACACTCCACACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:6565498..6565583 26863196 MeRIP-seq:(Medium) rs1256984789 Functional Loss SNV dbSNP153 33..33 33 - - - 74933 RMVar_ID_74933 Human_SNP_ID_687450650 m1A Human chr21 + 7775715 7775715 7775715 AAACAAACCCACAGAAAACAAACCCACAGACAACAAACCCACAGAAAACAAACCCGCAGAGAACA AAACAAACCCACAGAAAACAAACCCACAGACATCAAACCCACAGAAAACAAACCCGCAGAGAACA A T SMIM11B Ensembl:ENSG00000273590 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:7775664..7775779 26863196 MeRIP-seq:(Medium) rs1218445683 Functional Loss SNV dbSNP153 33..33 33 - - - 74934 RMVar_ID_74934 Human_SNP_ID_687514099 m1A Human chr21 - 8214731 8214726 8214731 CCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCCCGAGGGAGGACGCGGGGC CCGCCGCCGCCGCCACCGCCGCCGCCGCCCCG_____CGCGCCCTCCCGAGGGAGGACGCGGGGC GCGGGT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control chr21:8214376..8215180;chr21:8214351..8215325;chr21:8214626..8214825;chr21:8214624..8214850 26863410 MeRIP-seq:(Medium) rs1411672639 Functional Loss DEL dbSNP153 33..37 33 - - - 74935 RMVar_ID_74935 Human_SNP_ID_687514112 m1A Human chr21 - 8214749 8214734 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCC_______________CCGACCCGCGCGCCCTCC GGGCGGCGGCGGCGGT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1436058442 Functional Loss DEL dbSNP153 33..47 33 - - - 74936 RMVar_ID_74936 Human_SNP_ID_687514121 m1A Human chr21 - 8214749 8214737 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCC____________GCCCCGACCCGCGCGCCCTCC CGGCGGCGGCGGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1253438846 Functional Loss DEL dbSNP153 33..44 33 - - - 74937 RMVar_ID_74937 Human_SNP_ID_687514127 m1A Human chr21 - 8214749 8214740 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCC_________GCCGCCCCGACCCGCGCGCCCTCC CGGCGGCGGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1469592665 Functional Loss DEL dbSNP153 33..41 33 - - - 74938 RMVar_ID_74938 Human_SNP_ID_687514128 m1A Human chr21 - 8214749 8214743 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCC______GCCGCCGCCCCGACCCGCGCGCCCTCC CGGCGGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1319904619 Functional Loss DEL dbSNP153 33..38 33 - - - 74939 RMVar_ID_74939 Human_SNP_ID_687514132 m1A Human chr21 - 8214749 8214746 8214750 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGC____GCCGCCGCCGCCCCGACCCGCGCGCCCTCC CGGTG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1229181067 Functional Loss DEL dbSNP153 32..35 33 - - - 74940 RMVar_ID_74940 Human_SNP_ID_687514133 m1A Human chr21 - 8214749 8214746 8214750 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGC___CGCCGCCGCCGCCCCGACCCGCGCGCCCTCC CGGTG CG - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1229181067 Functional Loss DEL dbSNP153 32..34 33 - - - 74941 RMVar_ID_74941 Human_SNP_ID_687514143 m1A Human chr21 - 8214749 8214749 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1364575124 Functional Loss SNV dbSNP153 33..33 33 - - - 74942 RMVar_ID_74942 Human_SNP_ID_687514144 m1A Human chr21 - 8214749 8214749 8214749 GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC GTTTCGGTCCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGCCGCCGCCCCGACCCGCGCGCCCTCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214501..8214869 26863196 MeRIP-seq:(Medium) rs1364575124 Functional Loss SNV dbSNP153 33..33 33 - - - 74943 RMVar_ID_74943 Human_SNP_ID_687514210 m1A Human chr21 + 8214837 8214837 8214837 CCGGCAGCAGCACTCGCCGAATCCCGGGGCCGAGGGAGCGAGACCCGTCGCCGCGCTCTCCCCCC CCGGCAGCAGCACTCGCCGAATCCCGGGGCCGGGGGAGCGAGACCCGTCGCCGCGCTCTCCCCCC A G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:8214826..8214875 26863196 MeRIP-seq:(Medium) rs1473120830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5297516,Human_RBP_ID_22453933,Human_RBP_ID_22533665 RMVar_hsa_circ_18661 74944 RMVar_ID_74944 Human_SNP_ID_687514232 m1A Human chr21 + 8214881 8214881 8214881 CCGTCGCCGCGCTCTCCCCCCTCCCGGCGCCCACCCCCGCGGGGAATCCCCCGCGAGGGGGGTCT CCGTCGCCGCGCTCTCCCCCCTCCCGGCGCCCCCCCCCGCGGGGAATCCCCCGCGAGGGGGGTCT A C FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214876..8215525 26863196 MeRIP-seq:(Medium) rs1451348089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533709 RMVar_hsa_circ_18661 74945 RMVar_ID_74945 Human_SNP_ID_687514233 m1A Human chr21 + 8214881 8214881 8214881 CCGTCGCCGCGCTCTCCCCCCTCCCGGCGCCCACCCCCGCGGGGAATCCCCCGCGAGGGGGGTCT CCGTCGCCGCGCTCTCCCCCCTCCCGGCGCCCGCCCCCGCGGGGAATCCCCCGCGAGGGGGGTCT A G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8214876..8215525 26863196 MeRIP-seq:(Medium) rs1451348089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533709 RMVar_hsa_circ_18661 74946 RMVar_ID_74946 Human_SNP_ID_687514322 m1A Human chr21 - 8215027 8215026 8215027 CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCACCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGC_CCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8215026..8215375 26863196 MeRIP-seq:(Medium) rs1357366213 Functional Loss DEL dbSNP153 33..33 33 - - - 74947 RMVar_ID_74947 Human_SNP_ID_687514323 m1A Human chr21 - 8215027 8215027 8215027 CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCACCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCGCCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8215026..8215375 26863196 MeRIP-seq:(Medium) rs1276934720 Functional Loss SNV dbSNP153 33..33 33 - - - 74948 RMVar_ID_74948 Human_SNP_ID_687514324 m1A Human chr21 - 8215027 8215027 8215027 CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCACCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA CAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCCCCCCCCCCGTCGCCGGGGCGGGGGCGCGGGGA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8215026..8215375 26863196 MeRIP-seq:(Medium) rs1276934720 Functional Loss SNV dbSNP153 33..33 33 - - - 74949 RMVar_ID_74949 Human_SNP_ID_687514341 m1A Human chr21 + 8215056 8215056 8215056 GGGTGCCGCGCGCGGGTCGGGGGGCGGGGCGGACTGTCCCCAGTGCGCCCCGGGCGGGTCGCGCC GGGTGCCGCGCGCGGGTCGGGGGGCGGGGCGGGCTGTCCCCAGTGCGCCCCGGGCGGGTCGCGCC A G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:8215037..8215339 26863196 MeRIP-seq:(Medium) rs1205911054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18661 74950 RMVar_ID_74950 Human_SNP_ID_687514342 m1A Human chr21 + 8215056 8215056 8215056 GGGTGCCGCGCGCGGGTCGGGGGGCGGGGCGGACTGTCCCCAGTGCGCCCCGGGCGGGTCGCGCC GGGTGCCGCGCGCGGGTCGGGGGGCGGGGCGGTCTGTCCCCAGTGCGCCCCGGGCGGGTCGCGCC A T FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:8215037..8215339 26863196 MeRIP-seq:(Medium) rs1205911054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18661 74951 RMVar_ID_74951 Human_SNP_ID_687514344 m1A Human chr21 - 8215058 8215058 8215058 ACGGCGCGACCCGCCCGGGGCGCACTGGGGACAGTCCGCCCCGCCCCCCGACCCGCGCGCGGCAC ACGGCGCGACCCGCCCGGGGCGCACTGGGGACGGTCCGCCCCGCCCCCCGACCCGCGCGCGGCAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:8215026..8215100 26863196 MeRIP-seq:(Medium) rs1235784381 Functional Loss SNV dbSNP153 33..33 33 - - - 74952 RMVar_ID_74952 Human_SNP_ID_687514357 m1A Human chr21 - 8215082 8215082 8215082 CGAGAGAACCTCCCCCCGGGCCCGACGGCGCGACCCGCCCGGGGCGCACTGGGGACAGTCCGCCC CGAGAGAACCTCCCCCCGGGCCCGACGGCGCGTCCCGCCCGGGGCGCACTGGGGACAGTCCGCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:8215042..8215302;chr21:8215054..8215166 26863196 MeRIP-seq:(Medium) rs1253812030 Functional Loss SNV dbSNP153 33..33 33 - - - 74953 RMVar_ID_74953 Human_SNP_ID_687514388 m1A Human chr21 + 8215161 8215140 8215162 TCCCCCGAAGAGGGGGACGGCGGAGCGAGCGCACGGGGTCGGCGGCGACGTCGGCTACCCACCCG TCCCCCGAAGAG______________________GGGGTCGGCGGCGACGTCGGCTACCCACCCG GGGGGACGGCGGAGCGAGCGCAC G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:8215158..8215380 26863196 MeRIP-seq:(Medium) rs1340554160 Functional Loss DEL dbSNP153 13..34 33 - - - RMVar_hsa_circ_18661 74954 RMVar_ID_74954 Human_SNP_ID_687514447 m1A Human chr21 - 8216346 8216346 8216346 CGAGGGCAACGGAGGCCATCGCCCGTCCCTTCAGAACGGCGCTCGCCCATCTCTCAGGACCGACT CGAGGGCAACGGAGGCCATCGCCCGTCCCTTCGGAACGGCGCTCGCCCATCTCTCAGGACCGACT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:8216243..8216448 26863196 MeRIP-seq:(Medium) rs1280340320 Functional Loss SNV dbSNP153 33..33 33 - - - 74955 RMVar_ID_74955 Human_SNP_ID_687514499 m1A Human chr21 - 8216868 8216868 8216868 GCGCGCGCGGGGTGGGGCGGGGGAGGGCCGCGAGGGGGGTGCCCCGGGCGTGGGGGGGGCGGCGG GCGCGCGCGGGGTGGGGCGGGGGAGGGCCGCGTGGGGGGTGCCCCGGGCGTGGGGGGGGCGGCGG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:8216651..8217417 26863410 MeRIP-seq:(Medium) rs1163622890 Functional Loss SNV dbSNP153 33..33 33 - - - 74956 RMVar_ID_74956 Human_SNP_ID_687514515 m1A Human chr21 + 8216917 8216917 8216917 CCCACCCCGCGCGCGCCGCTCGCTCCCTCCCCACCCCGCGCCCTCTCTCTCTCTCTCTCCCCCGC CCCACCCCGCGCGCGCCGCTCGCTCCCTCCCCGCCCCGCGCCCTCTCTCTCTCTCTCTCCCCCGC A G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr21:8216851..8217100;chr21:8216807..8217144;chr21:8216805..8217145;chr21:8216813..8217042;chr21:8216806..8217483;chr21:8216801..8217151;chr21:8216855..8216978 26863196,32194978 MeRIP-seq:(Medium) rs1346640848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18661 74957 RMVar_ID_74957 Human_SNP_ID_687514731 m1A Human chr21 - 8217354 8217354 8217354 CCGCCGCCCGCCGCCGCCGCCGCGCGCCGAGGAGGAGGGGGGAACGGGGGGCGGACGGGGCCGGG CCGCCGCCCGCCGCCGCCGCCGCGCGCCGAGGGGGAGGGGGGAACGGGGGGCGGACGGGGCCGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:8217226..8217425 26863410 MeRIP-seq:(Medium) rs1160059241 Functional Loss SNV dbSNP153 33..33 33 - - - 74958 RMVar_ID_74958 Human_SNP_ID_687514746 m1A Human chr21 + 8217387 8217374 8217387 CCTCGGCGCGCGGCGGCGGCGGCGGGCGGCGGAGGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC CCTCGGCGCGCGGCGGCGGC_____________GGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC CGGCGGGCGGCGGA C FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8217376..8217400 26863196 MeRIP-seq:(Medium) rs1387083274 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_17670944,Human_RBP_ID_22601640,Human_RBP_ID_26788999 RMVar_hsa_circ_18661 74959 RMVar_ID_74959 Human_SNP_ID_687514763 m1A Human chr21 + 8217387 8217387 8217387 CCTCGGCGCGCGGCGGCGGCGGCGGGCGGCGGAGGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC CCTCGGCGCGCGGCGGCGGCGGCGGGCGGCGGCGGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC A C FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8217376..8217400 26863196 MeRIP-seq:(Medium) rs1283338434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17670944,Human_RBP_ID_22601640,Human_RBP_ID_26788999 RMVar_hsa_circ_18661 74960 RMVar_ID_74960 Human_SNP_ID_687514764 m1A Human chr21 + 8217387 8217387 8217387 CCTCGGCGCGCGGCGGCGGCGGCGGGCGGCGGAGGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC CCTCGGCGCGCGGCGGCGGCGGCGGGCGGCGGGGGGGCCGCGGGCCGGTCCCCCCCGCCGGGTCC A G FP671120.5 Ensembl:ENSG00000278996 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8217376..8217400 26863196 MeRIP-seq:(Medium) rs1283338434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17670944,Human_RBP_ID_22601640,Human_RBP_ID_26788999 RMVar_hsa_circ_18661 74961 RMVar_ID_74961 Human_SNP_ID_687517458 m1A Human chr21 - 8252204 8252204 8252204 GAAGGCCCTAGGCCCCCCCCGAGAACCCCCTCACGAGCCCCGGGGCCCCGCCACCGGGGGCCCCG GAAGGCCCTAGGCCCCCCCCGAGAACCCCCTCGCGAGCCCCGGGGCCCCGCCACCGGGGGCCCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:8252201..8252225 26863196 MeRIP-seq:(Medium) rs1367025951 Functional Loss SNV dbSNP153 33..33 33 - - - 74962 RMVar_ID_74962 Human_SNP_ID_687517459 m1A Human chr21 - 8252204 8252204 8252204 GAAGGCCCTAGGCCCCCCCCGAGAACCCCCTCACGAGCCCCGGGGCCCCGCCACCGGGGGCCCCG GAAGGCCCTAGGCCCCCCCCGAGAACCCCCTCCCGAGCCCCGGGGCCCCGCCACCGGGGGCCCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:8252201..8252225 26863196 MeRIP-seq:(Medium) rs1367025951 Functional Loss SNV dbSNP153 33..33 33 - - - 74963 RMVar_ID_74963 Human_SNP_ID_687517916 m1A Human chr21 - 8257218 8257218 8257218 ACCGCAGGCGGCGGCCACGGGAACTCGGCCCGAGCCGGCTCTCTCTTTCCCTCTCCGTCTTCGCG ACCGCAGGCGGCGGCCACGGGAACTCGGCCCGGGCCGGCTCTCTCTTTCCCTCTCCGTCTTCGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:8257212..8257406 26863196 MeRIP-seq:(Medium) rs1397970316 Functional Loss SNV dbSNP153 33..33 33 - - - 74964 RMVar_ID_74964 Human_SNP_ID_687517917 m1A Human chr21 + 8257226 8257226 8257226 CGGAGAGGGAAAGAGAGAGCCGGCTCGGGCCGAGTTCCCGTGGCCGCCGCCTGCGGTCCGGGTTC CGGAGAGGGAAAGAGAGAGCCGGCTCGGGCCGGGTTCCCGTGGCCGCCGCCTGCGGTCCGGGTTC A G KC876027,RNA28SN1-001,KC876027:2,KC876027:3,RNA5-8SN1,RNA28SN1-001:2,RNA28SN1-001:3,RNA28SN1-001:4,KC876027:4,RNA28SN1-001:5,RNA28SN1-001:6,AB372779-001,RNA28SN1-001:7,RNA28SN1-001:8,KC876027:5,RNA28SN1-001:9,KC876027:6,KC876027:7,KC876027:8,RNA18SN1-001,RNA28SN1-001:10,RNA28SN1-001:11,RNA28SN1-001:12,RNA28SN1-001:13 RNACentral:URS0000057950,RNACentral:URS00008FED4F,RNACentral:URS0000CA6044,RNACentral:URS00001A87D2,RNACentral:URS0000ABD8C6,RNACentral:URS0000CB738B,RNACentral:URS0000CBB795,RNACentral:URS00008C7E99,RNACentral:URS0000C9C917,RNACentral:URS0000E60B81,RNACentral:URS00008C7DAA,RNACentral:URS00002E16CD,RNACentral:URS000086853A,RNACentral:URS000043B91E,RNACentral:URS0000C90B2A,RNACentral:URS0000CAD839,RNACentral:URS0000C9C2FC,RNACentral:URS00002DFE82,RNACentral:URS00001C47AC,RNACentral:URS00008C90EE,RNACentral:URS00008CEEB7,RNACentral:URS0000CA7E3A,RNACentral:URS0000868511,RNACentral:URS0000CBCE18 misc_RNA,rRNA,misc_RNA,misc_RNA,rRNA,rRNA,rRNA,rRNA,misc_RNA,rRNA,rRNA,precursor RNA,rRNA,rRNA,misc_RNA,rRNA,misc_RNA,misc_RNA,misc_RNA,rRNA,rRNA,rRNA,rRNA,rRNA intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,exon,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:8257219..8257405 26863196 MeRIP-seq:(Medium) rs1351518656 Functional Loss SNV dbSNP153 33..33 33 - - - 74965 RMVar_ID_74965 Human_SNP_ID_687517938 m1A Human chr21 + 8257329 8257329 8257329 GGGGTCGGGGTTCGTCGGCCCCGGCCGGGTGGAAGGTCCCGTGCCCGTCGTCGTCGTCGTCGTCG GGGGTCGGGGTTCGTCGGCCCCGGCCGGGTGGGAGGTCCCGTGCCCGTCGTCGTCGTCGTCGTCG A G KC876027,RNA28SN1-001,KC876027:2,KC876027:3,RNA5-8SN1,RNA28SN1-001:2,RNA28SN1-001:3,RNA28SN1-001:4,KC876027:4,RNA28SN1-001:5,RNA28SN1-001:6,AB372779-001,RNA28SN1-001:7,RNA28SN1-001:8,KC876027:5,RNA28SN1-001:9,KC876027:6,KC876027:7,KC876027:8,RNA18SN1-001,RNA28SN1-001:10,RNA28SN1-001:11,RNA28SN1-001:12,RNA28SN1-001:13 RNACentral:URS0000057950,RNACentral:URS00008FED4F,RNACentral:URS0000CA6044,RNACentral:URS00001A87D2,RNACentral:URS0000ABD8C6,RNACentral:URS0000CB738B,RNACentral:URS0000CBB795,RNACentral:URS00008C7E99,RNACentral:URS0000C9C917,RNACentral:URS0000E60B81,RNACentral:URS00008C7DAA,RNACentral:URS00002E16CD,RNACentral:URS000086853A,RNACentral:URS000043B91E,RNACentral:URS0000C90B2A,RNACentral:URS0000CAD839,RNACentral:URS0000C9C2FC,RNACentral:URS00002DFE82,RNACentral:URS00001C47AC,RNACentral:URS00008C90EE,RNACentral:URS00008CEEB7,RNACentral:URS0000CA7E3A,RNACentral:URS0000868511,RNACentral:URS0000CBCE18 misc_RNA,rRNA,misc_RNA,misc_RNA,rRNA,rRNA,rRNA,rRNA,misc_RNA,rRNA,rRNA,precursor RNA,rRNA,rRNA,misc_RNA,rRNA,misc_RNA,misc_RNA,misc_RNA,rRNA,rRNA,rRNA,rRNA,rRNA intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,exon,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:8257326..8257350 26863196 MeRIP-seq:(Medium) rs1293896524 Functional Loss SNV dbSNP153 33..33 33 - - - 74966 RMVar_ID_74966 Human_SNP_ID_687518941 m1A Human chr21 + 8396252 8396252 8396252 TGGTGGTGGGGGAGGAGGAAGGCGGGTCCGGAAGGGGAAGGGTGCCGGCGGGGAGAGAGGGTCGG TGGTGGTGGGGGAGGAGGAAGGCGGGTCCGGAGGGGGAAGGGTGCCGGCGGGGAGAGAGGGTCGG A G FP236383.3 Ensembl:ENSG00000280441 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr21:8396250..8396338 26863410 MeRIP-seq:(Medium) rs1389279547 Functional Loss SNV dbSNP153 33..33 33 - - - 74967 RMVar_ID_74967 Human_SNP_ID_687519065 m1A Human chr21 - 8396629 8396629 8396629 GGAGCCGCCCCGCCCCGACGCGGAAGCTCGGGACGGGGCCCCGGCGCGGCGCGGCGCGGCCGCGA GGAGCCGCCCCGCCCCGACGCGGAAGCTCGGGGCGGGGCCCCGGCGCGGCGCGGCGCGGCCGCGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:8396600..8396746 26863410 MeRIP-seq:(Medium) rs1422697941 Functional Loss SNV dbSNP153 33..33 33 - - - 74968 RMVar_ID_74968 Human_SNP_ID_687519319 m1A Human chr21 + 8397585 8397585 8397585 CGGGGGTGGGGTCGGCGGGGGACCGTCCCCCGACCGGCGACCGGCCGCCGCCGGGCGCATTTCCA CGGGGGTGGGGTCGGCGGGGGACCGTCCCCCGGCCGGCGACCGGCCGCCGCCGGGCGCATTTCCA A G FP236383.3 Ensembl:ENSG00000280441 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:8397575..8398025 26863410 MeRIP-seq:(Medium) rs1161110099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10062,Human_RBP_ID_3961136,Human_RBP_ID_5089347,Human_RBP_ID_9332056 74969 RMVar_ID_74969 Human_SNP_ID_687519329 m1A Human chr21 - 8397716 8397711 8397716 AGGGAGGACGCGGGGCCGGGGCGGAGACGGGGAGGAGGAGGACGGACGGACGGACGGACGGGGCC AGGGAGGACGCGGGGCCGGGGCGGAGACGGGG_____GAGGACGGACGGACGGACGGACGGGGCC CCTCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8397451..8398475 26863196 MeRIP-seq:(Medium) rs1568901447 Functional Loss DEL dbSNP153 33..37 33 - - - 74970 RMVar_ID_74970 Human_SNP_ID_687519332 m1A Human chr21 - 8397716 8397714 8397716 AGGGAGGACGCGGGGCCGGGGCGGAGACGGGGAGGAGGAGGACGGACGGACGGACGGACGGGGCC AGGGAGGACGCGGGGCCGGGGCGGAGACGGGG__GAGGAGGACGGACGGACGGACGGACGGGGCC CCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:8397451..8398475 26863196 MeRIP-seq:(Medium) rs1192354009 Functional Loss DEL dbSNP153 33..34 33 - - - 74971 RMVar_ID_74971 Human_SNP_ID_687519380 m1A Human chr21 - 8402003 8401989 8402003 GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCACGCGCGCGCGCGCGCGCGCGCGGACAAACCCT GCCGGACGCGCACGCCCCGCCGGGCCCCCCGC______________GCGCGCGCGGACAAACCCT CGCGCGCGCGCGCGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8401990..8402208 26863196 MeRIP-seq:(Medium) rs1462904879 Functional Loss DEL dbSNP153 33..46 33 - - - 74972 RMVar_ID_74972 Human_SNP_ID_687519381 m1A Human chr21 - 8402003 8401991 8402003 GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCACGCGCGCGCGCGCGCGCGCGCGGACAAACCCT GCCGGACGCGCACGCCCCGCCGGGCCCCCCGC____________GCGCGCGCGCGGACAAACCCT CGCGCGCGCGCGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8401990..8402208 26863196 MeRIP-seq:(Medium) rs1203571591 Functional Loss DEL dbSNP153 33..44 33 - - - 74973 RMVar_ID_74973 Human_SNP_ID_687519391 m1A Human chr21 - 8402003 8401995 8402003 GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCACGCGCGCGCGCGCGCGCGCGCGGACAAACCCT GCCGGACGCGCACGCCCCGCCGGGCCCCCCGC________GCGCGCGCGCGCGCGGACAAACCCT CGCGCGCGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8401990..8402208 26863196 MeRIP-seq:(Medium) rs1357295080 Functional Loss DEL dbSNP153 33..40 33 - - - 74974 RMVar_ID_74974 Human_SNP_ID_687519398 m1A Human chr21 - 8402003 8402001 8402003 GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCACGCGCGCGCGCGCGCGCGCGCGGACAAACCCT GCCGGACGCGCACGCCCCGCCGGGCCCCCCGC__GCGCGCGCGCGCGCGCGCGCGGACAAACCCT CGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8401990..8402208 26863196 MeRIP-seq:(Medium) rs1446732476 Functional Loss DEL dbSNP153 33..34 33 - - - 74975 RMVar_ID_74975 Human_SNP_ID_687519400 m1A Human chr21 - 8402003 8402003 8402003 GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCACGCGCGCGCGCGCGCGCGCGCGGACAAACCCT GCCGGACGCGCACGCCCCGCCGGGCCCCCCGCGCGCGCGCGCGCGCGCGCGCGCGGACAAACCCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8401990..8402208 26863196 MeRIP-seq:(Medium) rs1244124613 Functional Loss SNV dbSNP153 33..33 33 - - - 74976 RMVar_ID_74976 Human_SNP_ID_687519414 m1A Human chr21 - 8402053 8402053 8402053 GTCGGCGGGAGAGGCCGGGAGGGAGGAAGACGAACGGAAGGACGGACGGCGCCGGACGCGCACGC GTCGGCGGGAGAGGCCGGGAGGGAGGAAGACGTACGGAAGGACGGACGGCGCCGGACGCGCACGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:8402051..8402175 26863196 MeRIP-seq:(Medium) rs1156999190 Functional Loss SNV dbSNP153 33..33 33 - - - 74977 RMVar_ID_74977 Human_SNP_ID_687521479 m1A Human chr21 + 8444130 8444130 8444130 CGAGGCGCCGCCGCCCCCCCCACGCCCGGGGCACCCCCCTCGCGGCCCTCCCCCGCCCCACCCCG CGAGGCGCCGCCGCCCCCCCCACGCCCGGGGCGCCCCCCTCGCGGCCCTCCCCCGCCCCACCCCG A G FP236383.3 Ensembl:ENSG00000280441 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:8444126..8444272 26863196 MeRIP-seq:(Medium) rs1297099968 Functional Loss SNV dbSNP153 33..33 33 - - - 74978 RMVar_ID_74978 Human_SNP_ID_687521494 m1A Human chr21 - 8444181 8444177 8444182 GGAGAGAGAGAGAGAGAGGGCGCGGGGCGGGGAGGGAGCGAGCGGCGCGCGCGGGGTGGGGCGGG GGAGAGAGAGAGAGAGAGGGCGCGGGGCGGG_____AGCGAGCGGCGCGCGCGGGGTGGGGCGGG TCCCTC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8444176..8444275 26863196 MeRIP-seq:(Medium) rs1252791034 Functional Loss DEL dbSNP153 32..36 33 - - - 74979 RMVar_ID_74979 Human_SNP_ID_687521495 m1A Human chr21 - 8444181 8444181 8444181 GGAGAGAGAGAGAGAGAGGGCGCGGGGCGGGGAGGGAGCGAGCGGCGCGCGCGGGGTGGGGCGGG GGAGAGAGAGAGAGAGAGGGCGCGGGGCGGGGCGGGAGCGAGCGGCGCGCGCGGGGTGGGGCGGG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:8444176..8444275 26863196 MeRIP-seq:(Medium) rs1212133589 Functional Loss SNV dbSNP153 33..33 33 - - - 74980 RMVar_ID_74980 Human_SNP_ID_687537609 m1A Human chr21 - 8553453 8553452 8553453 TGCCCAGGAGACACCCTATTTCCCTTTGTAAAACACCTCCTTCAACAAAAGGCAACTTCTCATGG TGCCCAGGAGACACCCTATTTCCCTTTGTAAA_CACCTCCTTCAACAAAAGGCAACTTCTCATGG GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:8553451..8553500 26863196 MeRIP-seq:(Medium) rs1163137251 Functional Loss DEL dbSNP153 33..33 33 - - - 74981 RMVar_ID_74981 Human_SNP_ID_687655357 m1A Human chr21 + 8988169 8988169 8988169 CGGCCGCGTCGGGGCCTCGCCGCGCTCTACCTACCTACCTGGTTGATCCTGCCAGTAGCATATGC CGGCCGCGTCGGGGCCTCGCCGCGCTCTACCTGCCTACCTGGTTGATCCTGCCAGTAGCATATGC A G KC876027,KC876027:2 RNACentral:URS0000057950,RNACentral:URS00002DFE82 misc_RNA,misc_RNA exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr21:8988061..8988279;chr21:8988061..8988281;chr21:8988075..8988255 26863196 MeRIP-seq:(Medium) rs1330179415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270429,Human_RBP_ID_281828,Human_RBP_ID_574543,Human_RBP_ID_1028236,Human_RBP_ID_1100847,Human_RBP_ID_1200535,Human_RBP_ID_1242114,Human_RBP_ID_1306582,Human_RBP_ID_1381834,Human_RBP_ID_1607182,Human_RBP_ID_1939363,Human_RBP_ID_2709712,Human_RBP_ID_3665221,Human_RBP_ID_4679621,Human_RBP_ID_5201859,Human_RBP_ID_5264247,Human_RBP_ID_5275854,Human_RBP_ID_5424168,Human_RBP_ID_5446212,Human_RBP_ID_5472600,Human_RBP_ID_5504189,Human_RBP_ID_5597301,Human_RBP_ID_7055156,Human_RBP_ID_8115504,Human_RBP_ID_8261453,Human_RBP_ID_8544993,Human_RBP_ID_8860564,Human_RBP_ID_9123701,Human_RBP_ID_9260460,Human_RBP_ID_9299173,Human_RBP_ID_10041144,Human_RBP_ID_10484340,Human_RBP_ID_14369796,Human_RBP_ID_17020010,Human_RBP_ID_17063962,Human_RBP_ID_17069065,Human_RBP_ID_17144801,Human_RBP_ID_17193398,Human_RBP_ID_17284459,Human_RBP_ID_17397732,Human_RBP_ID_17513987,Human_RBP_ID_17701475,Human_RBP_ID_17981246,Human_RBP_ID_18181478,Human_RBP_ID_18201411,Human_RBP_ID_18209539,Human_RBP_ID_18327292,Human_RBP_ID_18445092,Human_RBP_ID_18516297,Human_RBP_ID_18535001,Human_RBP_ID_18783721,Human_RBP_ID_19031837,Human_RBP_ID_20683802,Human_RBP_ID_21896032,Human_RBP_ID_21937226,Human_RBP_ID_22083017,Human_RBP_ID_22265351,Human_RBP_ID_22395953,Human_RBP_ID_22423107,Human_RBP_ID_22507521,Human_RBP_ID_22819233,Human_RBP_ID_23009586,Human_RBP_ID_23134191,Human_RBP_ID_23185876,Human_RBP_ID_23285114,Human_RBP_ID_23311866,Human_RBP_ID_23932930,Human_RBP_ID_24425779,Human_RBP_ID_24493496,Human_RBP_ID_24534067,Human_RBP_ID_24539033,Human_RBP_ID_24540320,Human_RBP_ID_25650158,Human_RBP_ID_26495918,Human_RBP_ID_26674524,Human_RBP_ID_26750336,Human_RBP_ID_27030719,Human_RBP_ID_27159246,Human_RBP_ID_27303624,Human_RBP_ID_27491136,Human_RBP_ID_27706527 74982 RMVar_ID_74982 Human_SNP_ID_687655375 m1A Human chr21 - 8988203 8988203 8988203 TACTTAGACATGCATGGCTTAATCTTTGAGACAAGCATATGCTACTGGCAGGATCAACCAGGTAG TACTTAGACATGCATGGCTTAATCTTTGAGACCAGCATATGCTACTGGCAGGATCAACCAGGTAG T G lnc-KCNE1B-10,lnc-KCNE1B-3,lnc-KCNE1B-3:2,lnc-KCNE1B-3:3,lnc-KCNE1B-3:4,lnc-KCNE1B-3:5,lnc-KCNE1B-3:6,lnc-KCNE1B-3:7,lnc-KCNE1B-3:8,lnc-KCNE1B-3:9 RNACentral:URS00004687BF,RNACentral:URS00008C2CD5,RNACentral:URS0000D591DD,RNACentral:URS0000D5E1BD,RNACentral:URS00008C1686,RNACentral:URS0000D58B87,RNACentral:URS0000D592AB,RNACentral:URS00008C2439,RNACentral:URS0000D59977,RNACentral:URS00008C389A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,intron,intron,exon,exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:8988101..8988225 26863410 MeRIP-seq:(Medium) rs1182863788 Functional Loss SNV dbSNP153 33..33 33 - - - 74983 RMVar_ID_74983 Human_SNP_ID_687655590 m1A Human chr21 + 8988683 8988683 8988683 GCGCAAATTACCCACTCCCGACCCGGGGAGGTAGTGACGAAAAATAACAATACAGGACTCTTTCG GCGCAAATTACCCACTCCCGACCCGGGGAGGTCGTGACGAAAAATAACAATACAGGACTCTTTCG A C RF01960-010,RF01960-010:2 RNACentral:URS0000955796,RNACentral:URS000023CAC4 rRNA,rRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1189731836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270453,Human_RBP_ID_281835,Human_RBP_ID_574543,Human_RBP_ID_1028244,Human_RBP_ID_1100862,Human_RBP_ID_1136363,Human_RBP_ID_1200545,Human_RBP_ID_1306592,Human_RBP_ID_1381844,Human_RBP_ID_1607190,Human_RBP_ID_1939368,Human_RBP_ID_2709717,Human_RBP_ID_3665231,Human_RBP_ID_4679624,Human_RBP_ID_5201899,Human_RBP_ID_5264263,Human_RBP_ID_5275862,Human_RBP_ID_5424190,Human_RBP_ID_5446194,Human_RBP_ID_5472615,Human_RBP_ID_5504206,Human_RBP_ID_5597308,Human_RBP_ID_7055164,Human_RBP_ID_8115512,Human_RBP_ID_8261455,Human_RBP_ID_8544999,Human_RBP_ID_8860571,Human_RBP_ID_9123727,Human_RBP_ID_9260469,Human_RBP_ID_9299183,Human_RBP_ID_10041152,Human_RBP_ID_10484348,Human_RBP_ID_14369913,Human_RBP_ID_17020102,Human_RBP_ID_17063969,Human_RBP_ID_17069043,Human_RBP_ID_17144806,Human_RBP_ID_17193406,Human_RBP_ID_17284469,Human_RBP_ID_17397740,Human_RBP_ID_17514010,Human_RBP_ID_17701487,Human_RBP_ID_17981267,Human_RBP_ID_18181498,Human_RBP_ID_18201375,Human_RBP_ID_18209579,Human_RBP_ID_18327301,Human_RBP_ID_18445101,Human_RBP_ID_18516301,Human_RBP_ID_18535008,Human_RBP_ID_18783730,Human_RBP_ID_20683822,Human_RBP_ID_21896038,Human_RBP_ID_21937232,Human_RBP_ID_22083020,Human_RBP_ID_22265353,Human_RBP_ID_22395954,Human_RBP_ID_22423108,Human_RBP_ID_22507527,Human_RBP_ID_22819237,Human_RBP_ID_23010415,Human_RBP_ID_23134201,Human_RBP_ID_23185878,Human_RBP_ID_23285129,Human_RBP_ID_23311920,Human_RBP_ID_23932933,Human_RBP_ID_24493502,Human_RBP_ID_24534074,Human_RBP_ID_24539043,Human_RBP_ID_24540326,Human_RBP_ID_25650165,Human_RBP_ID_26495940,Human_RBP_ID_26674529,Human_RBP_ID_26750305,Human_RBP_ID_27030719,Human_RBP_ID_27159251,Human_RBP_ID_27303632,Human_RBP_ID_27491150,Human_RBP_ID_27565051,Human_RBP_ID_27706533 74984 RMVar_ID_74984 Human_SNP_ID_687673694 m1A Human chr21 + 9043054 9043054 9043054 TTTGCCCCAGGTGTCTCACCTTCCCCTCATGGACCTTCTGACTTTCTGCACCTGCTCCGGCGCTG TTTGCCCCAGGTGTCTCACCTTCCCCTCATGGGCCTTCTGACTTTCTGCACCTGCTCCGGCGCTG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:9042999..9043136 26863410 MeRIP-seq:(Medium) rs1420075827 Functional Loss SNV dbSNP153 33..33 33 - - - 74985 RMVar_ID_74985 Human_SNP_ID_687684696 m1A Human chr21 - 9074890 9074890 9074890 GGCCCAGGAGGAGCCCCGGCTCCTGTGGCTGGAGTGAGGGTGCGGGCTGTGGTGGGAGAGGAGGT GGCCCAGGAGGAGCCCCGGCTCCTGTGGCTGGGGTGAGGGTGCGGGCTGTGGTGGGAGAGGAGGT T C TEKT4P2 Ensembl:ENSG00000188681 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:9074889..9075075 26863196 MeRIP-seq:(Medium) rs372596951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9123737 74986 RMVar_ID_74986 Human_SNP_ID_687684725 m1A Human chr21 + 9074923 9074923 9074923 CCAGCCACAGGAGCCGGGGCTCCTCCTGGGCCATTCCCACCACGCCGCCCAGGTCTCTCCAGCAC CCAGCCACAGGAGCCGGGGCTCCTCCTGGGCCGTTCCCACCACGCCGCCCAGGTCTCTCCAGCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:9074912..9075039 26863196 MeRIP-seq:(Medium) rs944228475 Functional Loss SNV dbSNP153 33..33 33 - - - 74987 RMVar_ID_74987 Human_SNP_ID_687684726 m1A Human chr21 + 9074923 9074923 9074923 CCAGCCACAGGAGCCGGGGCTCCTCCTGGGCCATTCCCACCACGCCGCCCAGGTCTCTCCAGCAC CCAGCCACAGGAGCCGGGGCTCCTCCTGGGCCTTTCCCACCACGCCGCCCAGGTCTCTCCAGCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:9074912..9075039 26863196 MeRIP-seq:(Medium) rs944228475 Functional Loss SNV dbSNP153 33..33 33 - - - 74988 RMVar_ID_74988 Human_SNP_ID_687690473 m1A Human chr21 - 9088029 9088029 9088029 CCGACCCCGGCCGACCCAGCCCCAAATCCCCTATCCAACCCCAAATCCCTGATCCAACCCCCAAT CCGACCCCGGCCGACCCAGCCCCAAATCCCCTGTCCAACCCCAAATCCCTGATCCAACCCCCAAT T C TEKT4P2 Ensembl:ENSG00000188681 Pseudogene intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:9087987..9088100 26863196 MeRIP-seq:(Medium) rs1187838464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17087157 74989 RMVar_ID_74989 Human_SNP_ID_687706942 m1A Human chr21 + 9129727 9129727 9129727 AGAACCAAGCCCCAGGCCTGCTCAGCTACACGACCGCCGCTGGGATCCGCACTTCCGGAGGAAAA AGAACCAAGCCCCAGGCCTGCTCAGCTACACGGCCGCCGCTGGGATCCGCACTTCCGGAGGAAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:9129488..9129731 26863196 MeRIP-seq:(Medium) rs1275576040 Functional Loss SNV dbSNP153 33..33 33 - - - 74990 RMVar_ID_74990 Human_SNP_ID_687732960 m1A Human chr21 - 9248125 9248125 9248125 CCAATCCACTCCACTCCACACCACTCCTCTCCATTCCATTCCGTTCCACTCCACCCCATTCCATT CCAATCCACTCCACTCCACACCACTCCTCTCCGTTCCATTCCGTTCCACTCCACCCCATTCCATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:9248113..9248340 26863196 MeRIP-seq:(Medium) rs1271253965 Functional Loss SNV dbSNP153 33..33 33 - - - 74991 RMVar_ID_74991 Human_SNP_ID_687765258 m1A Human chr21 - 9361800 9361800 9361800 GGCTGGAGAGATGGTCACAGTCTATGGGCTGCACAGGATGGAGGAGGCTGGGGAACAGGCAGGGT GGCTGGAGAGATGGTCACAGTCTATGGGCTGCTCAGGATGGAGGAGGCTGGGGAACAGGCAGGGT T A lnc-KCNE1B-2 RNACentral:URS00008BD811 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:9361749..9361814 26863196 MeRIP-seq:(Medium) rs1479339689 Functional Loss SNV dbSNP153 33..33 33 - - - 74992 RMVar_ID_74992 Human_SNP_ID_687767173 m1A Human chr21 + 9367601 9367601 9367601 CCTCTGACCAGGCCCTCACTGACCAGGCTCCAAGCCACTAAGGCCCCACACTGACCAGGCCCGTG CCTCTGACCAGGCCCTCACTGACCAGGCTCCATGCCACTAAGGCCCCACACTGACCAGGCCCGTG A T CR381653.1 Ensembl:ENSG00000278932 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:9367552..9367674 26863196 MeRIP-seq:(Medium) rs1466365786 Functional Loss SNV dbSNP153 33..33 33 - - - 74993 RMVar_ID_74993 Human_SNP_ID_688013587 m1A Human chr21 + 10119378 10119378 10119378 CGCGAATCCCGGCCTCCGGAGACCGTCCCGGTAACTACCCTGGCCGGGGCTGGTCTCAGCCCCGA CGCGAATCCCGGCCTCCGGAGACCGTCCCGGTGACTACCCTGGCCGGGGCTGGTCTCAGCCCCGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10119331..10119400 26863196 MeRIP-seq:(Medium) rs1368691624 Functional Loss SNV dbSNP153 33..33 33 - - - 74994 RMVar_ID_74994 Human_SNP_ID_688052792 m1A Human chr21 - 10378770 10378767 10378771 GGGAGAGAGGGAGGAGAGAGAGAGACAGAGACAGGGAGAGAGAGAGAGAGAGGAGAGAGACAGAA GGGAGAGAGGGAGGAGAGAGAGAGACAGAGA____GAGAGAGAGAGAGAGAGGAGAGAGACAGAA CCCTG C lnc-KCNE1B-6 RNACentral:URS00008B5D11 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10378691..10378900 26863196 MeRIP-seq:(Medium) rs1371510859 Functional Loss DEL dbSNP153 32..35 33 - - - 74995 RMVar_ID_74995 Human_SNP_ID_688052794 m1A Human chr21 - 10378770 10378768 10378770 GGGAGAGAGGGAGGAGAGAGAGAGACAGAGACAGGGAGAGAGAGAGAGAGAGGAGAGAGACAGAA GGGAGAGAGGGAGGAGAGAGAGAGACAGAGAC__GGAGAGAGAGAGAGAGAGGAGAGAGACAGAA CCT C lnc-KCNE1B-6 RNACentral:URS00008B5D11 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10378691..10378900 26863196 MeRIP-seq:(Medium) rs1311498865 Functional Loss DEL dbSNP153 33..34 33 - - - 74996 RMVar_ID_74996 Human_SNP_ID_688052798 m1A Human chr21 - 10378770 10378770 10378770 GGGAGAGAGGGAGGAGAGAGAGAGACAGAGACAGGGAGAGAGAGAGAGAGAGGAGAGAGACAGAA GGGAGAGAGGGAGGAGAGAGAGAGACAGAGACGGGGAGAGAGAGAGAGAGAGGAGAGAGACAGAA T C lnc-KCNE1B-6 RNACentral:URS00008B5D11 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10378691..10378900 26863196 MeRIP-seq:(Medium) rs867612589 Functional Loss SNV dbSNP153 33..33 33 - - - 74997 RMVar_ID_74997 Human_SNP_ID_688057239 m1A Human chr21 - 10396049 10396049 10396049 AGAGGGACAGATACAGAGATGGAGAGAAAGACAGAGACAGAGAGACACTAAGAGAGACACAGAGA AGAGGGACAGATACAGAGATGGAGAGAAAGACTGAGACAGAGAGACACTAAGAGAGACACAGAGA T A HSALNG0131846 RNACentral:URS0000EA75DD lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10395991..10396194 26863196 MeRIP-seq:(Medium) rs111212961 Functional Loss SNV dbSNP153 33..33 33 - - - 74998 RMVar_ID_74998 Human_SNP_ID_688057297 m1A Human chr21 + 10396344 10396344 10396344 TTCTGTCTCTTCATCTCTGTCTCGCTCTCTCTATGTATCTGTCTCTGTTTCTGCTTCTCTGTCTC TTCTGTCTCTTCATCTCTGTCTCGCTCTCTCTCTGTATCTGTCTCTGTTTCTGCTTCTCTGTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10396277..10396470 26863196 MeRIP-seq:(Medium) rs665796 Functional Loss SNV dbSNP153 33..33 33 - - - 74999 RMVar_ID_74999 Human_SNP_ID_688057298 m1A Human chr21 + 10396344 10396344 10396344 TTCTGTCTCTTCATCTCTGTCTCGCTCTCTCTATGTATCTGTCTCTGTTTCTGCTTCTCTGTCTC TTCTGTCTCTTCATCTCTGTCTCGCTCTCTCTGTGTATCTGTCTCTGTTTCTGCTTCTCTGTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10396277..10396470 26863196 MeRIP-seq:(Medium) rs665796 Functional Loss SNV dbSNP153 33..33 33 - - - 75000 RMVar_ID_75000 Human_SNP_ID_688057299 m1A Human chr21 - 10396349 10396348 10396350 AGACAGAGACAGAGAAGCAGAAACAGAGACAGATACATAGAGAGAGCGAGACAGAGATGAAGAGA AGACAGAGACAGAGAAGCAGAAACAGAGACA__TACATAGAGAGAGCGAGACAGAGATGAAGAGA ATC A HSALNG0131846 RNACentral:URS0000EA75DD lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:10396288..10396454 26863196 MeRIP-seq:(Medium) rs1309239086 Functional Loss DEL dbSNP153 32..33 33 - - - 75001 RMVar_ID_75001 Human_SNP_ID_688062181 m1A Human chr21 - 10412756 10412756 10412756 AGGGAAAGAAGACTGTGGGTAAAAAGATTTTGAGTGATGGAGGGGGGAAAAGGGTGACAAGTGGG AGGGAAAGAAGACTGTGGGTAAAAAGATTTTGCGTGATGGAGGGGGGAAAAGGGTGACAAGTGGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10412386..10412833 26863196 MeRIP-seq:(Medium) rs1317990279 Functional Loss SNV dbSNP153 33..33 33 - - - 75002 RMVar_ID_75002 Human_SNP_ID_688062588 m1A Human chr21 + 10413691 10413689 10413691 CAGCGCAGCTGGAGTGTTAGGAGGGCGGCCTGAGCGGTAGGAGTGGGGCTGGAGCAGTAAGATGG CAGCGCAGCTGGAGTGTTAGGAGGGCGGCCT__GCGGTAGGAGTGGGGCTGGAGCAGTAAGATGG TGA T BAGE2 Ensembl:ENSG00000187172 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:10413504..10413831;chr21:10413555..10414881 26863196 MeRIP-seq:(Medium) rs754541032 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22602305,Human_RBP_ID_26344188,Human_RBP_ID_27840750 Human_Splice_Rec_2107237,Human_Splice_Rec_2107241 75003 RMVar_ID_75003 Human_SNP_ID_688064985 m1A Human chr21 - 10426633 10426633 10426633 CCACCACCACCACTACCACCACCATCACCACCACCACCATCACCATCACCACCACCACCACCATC CCACCACCACCACTACCACCACCATCACCACCGCCACCATCACCATCACCACCACCACCACCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10426629..10426701 26863196 MeRIP-seq:(Medium) rs1190141951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211430,RMVar_hsa_circ_97300 75004 RMVar_ID_75004 Human_SNP_ID_688065213 m1A Human chr21 - 10426806 10426777 10426807 CCACCACCATCACCACTACCACCACCACCACTACCACCACCACCAGCACCACCACCATCACCACT CCACCACCATCACCACTACCACCACCACCAC______________________________CACT GGTGATGGTGGTGGTGCTGGTGGTGGTGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10426799..10426876 26863196 MeRIP-seq:(Medium) rs1268635279 Functional Loss DEL dbSNP153 32..61 33 - - - Human_RBP_ID_9432779 RMVar_hsa_circ_211430,RMVar_hsa_circ_97300 75005 RMVar_ID_75005 Human_SNP_ID_688065253 m1A Human chr21 - 10426806 10426792 10426807 CCACCACCATCACCACTACCACCACCACCACTACCACCACCACCAGCACCACCACCATCACCACT CCACCACCATCACCACTACCACCACCACCAC_______________CACCACCACCATCACCACT GCTGGTGGTGGTGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10426799..10426876 26863196 MeRIP-seq:(Medium) rs1568917642 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_9432779 RMVar_hsa_circ_211430,RMVar_hsa_circ_97300 75006 RMVar_ID_75006 Human_SNP_ID_688065279 m1A Human chr21 - 10426806 10426804 10426807 CCACCACCATCACCACTACCACCACCACCACTACCACCACCACCAGCACCACCACCATCACCACT CCACCACCATCACCACTACCACCACCACCAC___CACCACCACCAGCACCACCACCATCACCACT GGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10426799..10426876 26863196 MeRIP-seq:(Medium) rs750574634 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9432779 RMVar_hsa_circ_211430,RMVar_hsa_circ_97300 75007 RMVar_ID_75007 Human_SNP_ID_688087964 m1A Human chr21 + 10521479 10521479 10521479 GTCCCGGAGGCGGAGTCTGCGGCGGCGGGCGGAACGGGGGCGCGCCTATGCTAGTCACGTGGGCG GTCCCGGAGGCGGAGTCTGCGGCGGCGGGCGGGACGGGGGCGCGCCTATGCTAGTCACGTGGGCG A G AF254983.1 Ensembl:ENSG00000273840 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:10521432..10521521 26863196 MeRIP-seq:(Medium) rs1326205750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54319,RMVar_hsa_circ_353932,RMVar_hsa_circ_367182,RMVar_hsa_circ_358105 75008 RMVar_ID_75008 Human_SNP_ID_688133190 m1A Human chr21 + 10617382 10617381 10617383 AAGAGAGAATGGTAAAAGGGAGGAAGGCAAAGACACGAAGAAAATAAAGAGGAGAAGGAAGGAAA AAGAGAGAATGGTAAAAGGGAGGAAGGCAAAG__ACGAAGAAAATAAAGAGGAGAAGGAAGGAAA GAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:10617240..10617674 26863196 MeRIP-seq:(Medium) rs1314881260 Functional Loss DEL dbSNP153 33..34 33 - - - 75009 RMVar_ID_75009 Human_SNP_ID_688133247 m1A Human chr21 + 10617476 10617474 10617477 AGAAAAGGAGGGAGGAAGGGAGAAAAAAGGAAAGAAAGCAACAAAGTGAGAAAGAATAAGAGAAA AGAAAAGGAGGGAGGAAGGGAGAAAAAAGGA___AAAGCAACAAAGTGAGAAAGAATAAGAGAAA AAAG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10617309..10617709 26863196 MeRIP-seq:(Medium) rs1469155324 Functional Loss DEL dbSNP153 32..34 33 - - - 75010 RMVar_ID_75010 Human_SNP_ID_688153399 m1A Human chr21 + 10655568 10655564 10655569 AGATTCCACTCCATTCCATTCCATTCGAGTCCATTCCATTCCATTCCATTCCATTCCGTTCCGTT AGATTCCACTCCATTCCATTCCATTCGAG_____TCCATTCCATTCCATTCCATTCCGTTCCGTT GTCCAT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10655518..10655648 26863196 MeRIP-seq:(Medium) rs147396674 Functional Loss DEL dbSNP153 30..34 33 - - - 75011 RMVar_ID_75011 Human_SNP_ID_688153833 m1A Human chr21 - 10656353 10656334 10656353 GGAATGGAATGGAATGGAATTGAATGGAATGGAGTGGAATGGAATTGAATGGAGTGGAATGGAAT GGAATGGAATGGAATGGAATTGAATGGAATGG___________________GAGTGGAATGGAAT CCATTCAATTCCATTCCACT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10656303..10656431 26863196 MeRIP-seq:(Medium) rs1446375155 Functional Loss DEL dbSNP153 33..51 33 - - - 75012 RMVar_ID_75012 Human_SNP_ID_688153846 m1A Human chr21 - 10656353 10656353 10656353 GGAATGGAATGGAATGGAATTGAATGGAATGGAGTGGAATGGAATTGAATGGAGTGGAATGGAAT GGAATGGAATGGAATGGAATTGAATGGAATGGGGTGGAATGGAATTGAATGGAGTGGAATGGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10656303..10656431 26863196 MeRIP-seq:(Medium) rs796515636 Functional Loss SNV dbSNP153 33..33 33 - - - 75013 RMVar_ID_75013 Human_SNP_ID_688155139 m1A Human chr21 - 10658636 10658636 10658636 AATGGAATGGATTTGAATGGAATGGACTCGAAAGGAATGGAATGGAATTTAATGGAATGGAATCT AATGGAATGGATTTGAATGGAATGGACTCGAATGGAATGGAATGGAATTTAATGGAATGGAATCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10658630..10658714 26863196 MeRIP-seq:(Medium) rs147966278 Functional Loss SNV dbSNP153 33..33 33 - - - 75014 RMVar_ID_75014 Human_SNP_ID_688155935 m1A Human chr21 + 10659949 10659949 10659949 TTCCATTCGGGTCCATTCAATTCCATTCCATTAGGGTCCATTCCATTCCATTCCACTCCATTCGG TTCCATTCGGGTCCATTCAATTCCATTCCATTCGGGTCCATTCCATTCCATTCCACTCCATTCGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10659948..10660127 26863196 MeRIP-seq:(Medium) rs550615684 Functional Loss SNV dbSNP153 33..33 33 - - - 75015 RMVar_ID_75015 Human_SNP_ID_688163736 m1A Human chr21 - 10673283 10673281 10673283 GAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATCAACAGGAATGGAATGGAATG GAATGGAATGGAATGGAATGGAATGGAATGGA__GGAATGGAATCAACAGGAATGGAATGGAATG CAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10673224..10673351 26863196 MeRIP-seq:(Medium) rs60214102 Functional Loss DEL dbSNP153 33..34 33 - - - 75016 RMVar_ID_75016 Human_SNP_ID_688164216 m1A Human chr21 - 10674124 10674124 10674124 GGAATGGACTCGAATGGAATGGAATGGACTGAAATGGAATAGAATGGAATGGAATGGACTCGAAT GGAATGGACTCGAATGGAATGGAATGGACTGATATGGAATAGAATGGAATGGAATGGACTCGAAT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10674122..10674225 26863196 MeRIP-seq:(Medium) rs200159402 Functional Loss SNV dbSNP153 33..33 33 - - - 75017 RMVar_ID_75017 Human_SNP_ID_688164217 m1A Human chr21 - 10674124 10674124 10674124 GGAATGGACTCGAATGGAATGGAATGGACTGAAATGGAATAGAATGGAATGGAATGGACTCGAAT GGAATGGACTCGAATGGAATGGAATGGACTGACATGGAATAGAATGGAATGGAATGGACTCGAAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10674122..10674225 26863196 MeRIP-seq:(Medium) rs200159402 Functional Loss SNV dbSNP153 33..33 33 - - - 75018 RMVar_ID_75018 Human_SNP_ID_688165965 m1A Human chr21 - 10676833 10676833 10676833 ATTGGAATAGAATGGAATGGAATGGAAAGGAAAGGTATGGAATGGAATGGAATGGAATTTAAATG ATTGGAATAGAATGGAATGGAATGGAAAGGAATGGTATGGAATGGAATGGAATGGAATTTAAATG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10676825..10676916 26863196 MeRIP-seq:(Medium) rs1414687605 Functional Loss SNV dbSNP153 33..33 33 - - - 75019 RMVar_ID_75019 Human_SNP_ID_688174438 m1A Human chr21 + 10689954 10689954 10689954 ATTTTCCATAACATTCCATTCCATTTGGGTGCATTCCATGGCATTCAATTCAAGTCCAGTATATT ATTTTCCATAACATTCCATTCCATTTGGGTGCGTTCCATGGCATTCAATTCAAGTCCAGTATATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10689951..10690035 26863196 MeRIP-seq:(Medium) rs532801523 Functional Loss SNV dbSNP153 33..33 33 - - - 75020 RMVar_ID_75020 Human_SNP_ID_688201200 m1A Human chr21 - 10736340 10736340 10736340 GAAAGGAATGGAATGGAATTTAGTGGAGTGGAATGGAATGGAATGGAATGGAATGGAGTCGAATA GAAAGGAATGGAATGGAATTTAGTGGAGTGGATTGGAATGGAATGGAATGGAATGGAGTCGAATA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10736309..10736402 26863196 MeRIP-seq:(Medium) rs868441893 Functional Loss SNV dbSNP153 33..33 33 - - - 75021 RMVar_ID_75021 Human_SNP_ID_688201201 m1A Human chr21 - 10736340 10736340 10736340 GAAAGGAATGGAATGGAATTTAGTGGAGTGGAATGGAATGGAATGGAATGGAATGGAGTCGAATA GAAAGGAATGGAATGGAATTTAGTGGAGTGGAGTGGAATGGAATGGAATGGAATGGAGTCGAATA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10736309..10736402 26863196 MeRIP-seq:(Medium) rs868441893 Functional Loss SNV dbSNP153 33..33 33 - - - 75022 RMVar_ID_75022 Human_SNP_ID_688201202 m1A Human chr21 - 10736340 10736340 10736340 GAAAGGAATGGAATGGAATTTAGTGGAGTGGAATGGAATGGAATGGAATGGAATGGAGTCGAATA GAAAGGAATGGAATGGAATTTAGTGGAGTGGACTGGAATGGAATGGAATGGAATGGAGTCGAATA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:10736309..10736402 26863196 MeRIP-seq:(Medium) rs868441893 Functional Loss SNV dbSNP153 33..33 33 - - - 75023 RMVar_ID_75023 Human_SNP_ID_688569145 m1A Human chr21 + 14055776 14055776 14055776 GACACATCCAAGTCCAGGAAAGGGCTAGGGCCATGACAGAGCCAGGGTGAGTCCTTGGCAGGGCC GACACATCCAAGTCCAGGAAAGGGCTAGGGCCGTGACAGAGCCAGGGTGAGTCCTTGGCAGGGCC A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14055729..14055795 26863196 MeRIP-seq:(Medium) rs1334055709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24380634 75024 RMVar_ID_75024 Human_SNP_ID_688569279 m1A Human chr21 + 14056279 14056279 14056279 GACAGGACAAGGACCAGGGCAAGGGCATGCCCAGGGCAGAGGTAGGGCCAGAGCCAGGGTCTGGG GACAGGACAAGGACCAGGGCAAGGGCATGCCCGGGGCAGAGGTAGGGCCAGAGCCAGGGTCTGGG A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14056059..14056464 26863196 MeRIP-seq:(Medium) rs1269696643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22601665 75025 RMVar_ID_75025 Human_SNP_ID_688569768 m1A Human chr21 - 14057909 14057909 14057909 CATGGTCCTGCCATGTTTCTTGCCCTGTCCCTATCCTGGCCCTGGCCCTGACCCTTACCCTGGTC CATGGTCCTGCCATGTTTCTTGCCCTGTCCCTGTCCTGGCCCTGGCCCTGACCCTTACCCTGGTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:14057788..14057935 26863196 MeRIP-seq:(Medium) rs951420344 Functional Loss SNV dbSNP153 33..33 33 - - - 75026 RMVar_ID_75026 Human_SNP_ID_688569865 m1A Human chr21 - 14058208 14058208 14058208 GCCCCTACCATTGCCTTGCCCTGTTCTGCCTCATCCTGGCACTGACCCGGCCATGCCATTGCCCT GCCCCTACCATTGCCTTGCCCTGTTCTGCCTCGTCCTGGCACTGACCCGGCCATGCCATTGCCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:14058127..14058248 26863196 MeRIP-seq:(Medium) rs943099435 Functional Loss SNV dbSNP153 33..33 33 - - - 75027 RMVar_ID_75027 Human_SNP_ID_688570073 m1A Human chr21 - 14058822 14058822 14058822 CCTGCCCTGGTTGTGCCCTGGCCCTGCCTGGCACTGGCCGCTCCCTGGACCTGCCCTGACCCTGC CCTGCCCTGGTTGTGCCCTGGCCCTGCCTGGCGCTGGCCGCTCCCTGGACCTGCCCTGACCCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:14058699..14058908;chr21:14058607..14058896 26863196 MeRIP-seq:(Medium) rs373447530 Functional Loss SNV dbSNP153 33..33 33 - - - 75028 RMVar_ID_75028 Human_SNP_ID_688570198 m1A Human chr21 - 14059100 14059100 14059100 GCCCTGGACCTTCCCTGAATCTGCGCTGACCCAGCTTTGGCTCTGGCCCTGCCTCCTGTCCTGAT GCCCTGGACCTTCCCTGAATCTGCGCTGACCCTGCTTTGGCTCTGGCCCTGCCTCCTGTCCTGAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:14059050..14059292 26863196 MeRIP-seq:(Medium) rs1357772320 Functional Loss SNV dbSNP153 33..33 33 - - - 75029 RMVar_ID_75029 Human_SNP_ID_688570202 m1A Human chr21 - 14059104 14059104 14059104 CTCTGCCCTGGACCTTCCCTGAATCTGCGCTGACCCAGCTTTGGCTCTGGCCCTGCCTCCTGTCC CTCTGCCCTGGACCTTCCCTGAATCTGCGCTGCCCCAGCTTTGGCTCTGGCCCTGCCTCCTGTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:14059055..14059218 26863196 MeRIP-seq:(Medium) rs1210640888 Functional Loss SNV dbSNP153 33..33 33 - - - 75030 RMVar_ID_75030 Human_SNP_ID_688571385 m1A Human chr21 + 14062623 14062623 14062623 AAGGTGATGGGGTAGATGCGCTATCCCGGGCTACATTGCCCGCGGCCGGGGGCTGCTAGGGGTGT AAGGTGATGGGGTAGATGCGCTATCCCGGGCTGCATTGCCCGCGGCCGGGGGCTGCTAGGGGTGT A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14062574..14062665 26863196 MeRIP-seq:(Medium) rs964558333 Functional Loss SNV dbSNP153 33..33 33 - - - 75031 RMVar_ID_75031 Human_SNP_ID_688577122 m1A Human chr21 + 14077184 14077180 14077185 AAACAAAGGAAAGAAAAAAGAAAGAAGAAAAAAGAAAAAGAATAAAAGGCAGAAAGAAGAAAGGA AAACAAAGGAAAGAAAAAAGAAAGAAGAA_____AAAAAGAATAAAAGGCAGAAAGAAGAAAGGA AAAAAG A AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14076858..14077320 26863196 MeRIP-seq:(Medium) rs1174915430 Functional Loss DEL dbSNP153 30..34 33 - - - 75032 RMVar_ID_75032 Human_SNP_ID_688577125 m1A Human chr21 + 14077190 14077189 14077191 AGGAAAGAAAAAAGAAAGAAGAAAAAAGAAAAAGAATAAAAGGCAGAAAGAAGAAAGGAAAGAAA AGGAAAGAAAAAAGAAAGAAGAAAAAAGAAAA__AATAAAAGGCAGAAAGAAGAAAGGAAAGAAA AAG A AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:14076873..14077315 26863196 MeRIP-seq:(Medium) rs1424954028 Functional Loss DEL dbSNP153 33..34 33 - - - 75033 RMVar_ID_75033 Human_SNP_ID_688577696 m1A Human chr21 + 14078066 14078066 14078066 GAAAGAGAGAAAGAAGAAAGAAAGGAAAAAGGAAGGAAGAAAAAGAAAGGAAAAAGGAAATAGAA GAAAGAGAGAAAGAAGAAAGAAAGGAAAAAGGGAGGAAGAAAAAGAAAGGAAAAAGGAAATAGAA A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14078015..14078089 26863196 MeRIP-seq:(Medium) rs1263235829 Functional Loss SNV dbSNP153 33..33 33 - - - 75034 RMVar_ID_75034 Human_SNP_ID_688577758 m1A Human chr21 + 14078134 14078134 14078134 GAAAAAAGAAAGAGAAAGAAAGAGGGAACTGGAGAAATTAAGAAGACAGAAATGAAAGGAGAAAG GAAAAAAGAAAGAGAAAGAAAGAGGGAACTGGTGAAATTAAGAAGACAGAAATGAAAGGAGAAAG A T AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:14077999..14078252 26863196 MeRIP-seq:(Medium) rs1385738072 Functional Loss SNV dbSNP153 33..33 33 - - - 75035 RMVar_ID_75035 Human_SNP_ID_688614367 m1A Human chr21 - 14216188 14216188 14216188 CGGTCCTGTCGGCCTCCTCCTGAGCAGGGAACATCCTCCGGTCTCGGCCGTAGAATGAAGTAGGA CGGTCCTGTCGGCCTCCTCCTGAGCAGGGAACGTCCTCCGGTCTCGGCCGTAGAATGAAGTAGGA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr21:14216181..14216265 26863410 MeRIP-seq:(Medium) rs1199461694 Functional Loss SNV dbSNP153 33..33 33 - - - 75036 RMVar_ID_75036 Human_SNP_ID_688655746 m1A Human chr21 - 14373212 14373212 14373212 ATTAGCAGGAGCTGGTAATTACTTGTATTATCACATGTAACTAATAATTTGAACTATACTTGAAG ATTAGCAGGAGCTGGTAATTACTTGTATTATCGCATGTAACTAATAATTTGAACTATACTTGAAG T C HSPA13 Ensembl:ENSG00000155304 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:14373161..14373261 32194978 MeRIP-seq:(Medium) rs929724829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569516,Human_RBP_ID_1027329,Human_RBP_ID_1601496,Human_RBP_ID_8539285,Human_RBP_ID_9120219,Human_RBP_ID_17513121,Human_RBP_ID_22395632,Human_RBP_ID_23918934,Human_RBP_ID_27704337 Human_miRNA_ID_1978123,Human_miRNA_ID_3121805 RMVar_hsa_circ_108573,RMVar_hsa_circ_211447,RMVar_hsa_circ_211449,RMVar_hsa_circ_91622,RMVar_hsa_circ_211448 75037 RMVar_ID_75037 Human_SNP_ID_688655897 m1A Human chr21 + 14373811 14373811 14373811 AATGACTTGACGGATCCGAGGAATACGAGTGGAGCCCCCAACTAAAACCACCTCATCAATCTCAG AATGACTTGACGGATCCGAGGAATACGAGTGGTGCCCCCAACTAAAACCACCTCATCAATCTCAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:14373560..14373910 32194978 MeRIP-seq:(Medium) rs1294148280 Functional Loss SNV dbSNP153 33..33 33 - - - 75038 RMVar_ID_75038 Human_SNP_ID_688657842 m1A Human chr21 - 14381345 14381345 14381345 TATCAGCATACCCAGCATGGTGTCTTTTACTGACAATGATGTATATGTGGGATATGAAAGCGTAG TATCAGCATACCCAGCATGGTGTCTTTTACTGGCAATGATGTATATGTGGGATATGAAAGCGTAG T C HSPA13 Ensembl:ENSG00000155304 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:14381294..14381495 32194978 MeRIP-seq:(Medium) rs1029748331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1601551,Human_RBP_ID_1933420,Human_RBP_ID_9120227,Human_RBP_ID_14187960,Human_RBP_ID_22395652,Human_RBP_ID_22767776,Human_RBP_ID_23918957,Human_RBP_ID_27025436,Human_RBP_ID_27300394 Human_miRNA_ID_2885869 RMVar_hsa_circ_108573,RMVar_hsa_circ_211449 75039 RMVar_ID_75039 Human_SNP_ID_688784574 m1A Human chr21 + 14857697 14857697 14857697 CCAGCAAACTGGAAAGGGTGTGTTCTCGTGGCAGGGGCAGGAGTCTACAAAAGAAAGCAGAAATG CCAGCAAACTGGAAAGGGTGTGTTCTCGTGGCGGGGGCAGGAGTCTACAAAAGAAAGCAGAAATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:14857681..14857753 26863196 MeRIP-seq:(Medium) rs1409079391 Functional Loss SNV dbSNP153 33..33 33 - - - 75040 RMVar_ID_75040 Human_SNP_ID_688836966 m1A Human chr21 - 15064816 15064816 15064816 TCGGAGGGAAGAGCTCGCCGGGGCGCCGGGCCAGGACGGGGCGGCAGGCGCCTTCGCGGACCGAG TCGGAGGGAAGAGCTCGCCGGGGCGCCGGGCCTGGACGGGGCGGCAGGCGCCTTCGCGGACCGAG T A NRIP1 Ensembl:ENSG00000180530 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:15064776..15065000 26863196 MeRIP-seq:(Medium) rs1161601886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679693,Human_RBP_ID_5240576,Human_RBP_ID_5323477,Human_RBP_ID_8860585,Human_RBP_ID_9332074,Human_RBP_ID_9391326,Human_RBP_ID_17144828,Human_RBP_ID_18423339,Human_RBP_ID_23009617 Human_Splice_Rec_2108301,Human_Splice_Rec_2108305,Human_Splice_Rec_2108309 75041 RMVar_ID_75041 Human_SNP_ID_688836976 m1A Human chr21 + 15064834 15064834 15064834 CTGCCGCCCCGTCCTGGCCCGGCGCCCCGGCGAGCTCTTCCCTCCGACCAGCGGCGCTCACGGCG CTGCCGCCCCGTCCTGGCCCGGCGCCCCGGCGGGCTCTTCCCTCCGACCAGCGGCGCTCACGGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:15064681..15065046 26863196 MeRIP-seq:(Medium) rs1326596193 Functional Loss SNV dbSNP153 33..33 33 - - - 75042 RMVar_ID_75042 Human_SNP_ID_688836982 m1A Human chr21 + 15064851 15064851 15064851 CCCGGCGCCCCGGCGAGCTCTTCCCTCCGACCAGCGGCGCTCACGGCGCAGCGGCGGACGCGAGG CCCGGCGCCCCGGCGAGCTCTTCCCTCCGACCGGCGGCGCTCACGGCGCAGCGGCGGACGCGAGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:15064801..15065000 26863196 MeRIP-seq:(Medium) rs1165611210 Functional Loss SNV dbSNP153 33..33 33 - - - 75043 RMVar_ID_75043 Human_SNP_ID_689012257 m1A Human chr21 + 15730044 15730044 15730044 TCTCCCTTCCCCAAAGCAGCCCGCGGACCGGCAGCAAAGGAACGTGCGAACGCGTGACGCCGCCC TCTCCCTTCCCCAAAGCAGCCCGCGGACCGGCCGCAAAGGAACGTGCGAACGCGTGACGCCGCCC A C USP25 Ensembl:ENSG00000155313 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:15729993..15730174 26863196 MeRIP-seq:(Medium) rs1450480670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4666331 75044 RMVar_ID_75044 Human_SNP_ID_689012350 m1A Human chr21 - 15730304 15730304 15730304 CCGGCCCTGGCTGCCGCGCTCCGCCGAGCTCCAGGGAGCGGCGCGGACGGCCTGGGAGGACAGCG CCGGCCCTGGCTGCCGCGCTCCGCCGAGCTCCGGGGAGCGGCGCGGACGGCCTGGGAGGACAGCG T C lnc-NRIP1-9 RNACentral:URS00008B56B8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:15730254..15730387 26863196 MeRIP-seq:(Medium) rs931917903 Functional Loss SNV dbSNP153 33..33 33 - - - 75045 RMVar_ID_75045 Human_SNP_ID_689012379 m1A Human chr21 + 15730361 15730356 15730362 AGGGCCGGCGGAGGCGCGAGGAGCCGGGCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC AGGGCCGGCGGAGGCGCGAGGAGCCGGG______CGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC GCGCCAC G USP25 Ensembl:ENSG00000155313 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr21:15730326..15730483;chr21:15730323..15730424 26863196 MeRIP-seq:(Medium) rs1555817369 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_4679697,Human_RBP_ID_8860822,Human_RBP_ID_9299189 Human_Splice_Rec_2108603,Human_Splice_Rec_2108649,Human_Splice_Rec_2108669,Human_Splice_Rec_2108717 75046 RMVar_ID_75046 Human_SNP_ID_689012383 m1A Human chr21 + 15730361 15730358 15730361 AGGGCCGGCGGAGGCGCGAGGAGCCGGGCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC AGGGCCGGCGGAGGCGCGAGGAGCCGGGCG___CCGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC GCCA G USP25 Ensembl:ENSG00000155313 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr21:15730326..15730483;chr21:15730323..15730424 26863196 MeRIP-seq:(Medium) rs529419094 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4679697,Human_RBP_ID_8860822,Human_RBP_ID_9299189 Human_Splice_Rec_2108603,Human_Splice_Rec_2108649,Human_Splice_Rec_2108669,Human_Splice_Rec_2108717 75047 RMVar_ID_75047 Human_SNP_ID_689012387 m1A Human chr21 + 15730361 15730361 15730361 AGGGCCGGCGGAGGCGCGAGGAGCCGGGCGCCACCGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC AGGGCCGGCGGAGGCGCGAGGAGCCGGGCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGGGGGCC A G USP25 Ensembl:ENSG00000155313 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr21:15730326..15730483;chr21:15730323..15730424 26863196 MeRIP-seq:(Medium) rs771601190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679697,Human_RBP_ID_8860822,Human_RBP_ID_9299189 Human_Splice_Rec_2108603,Human_Splice_Rec_2108649,Human_Splice_Rec_2108669,Human_Splice_Rec_2108717 75048 RMVar_ID_75048 Human_SNP_ID_689019180 m1A Human chr21 - 15755845 15755845 15755845 CCTCCACTTCTCCCTTTATGAAGAGGGGATTCAGGCTTCAATCATCTGGCCCTTTTTAGAGCCTC CCTCCACTTCTCCCTTTATGAAGAGGGGATTCGGGCTTCAATCATCTGGCCCTTTTTAGAGCCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:15755842..15755984 26863196 MeRIP-seq:(Medium) rs952030930 Functional Loss SNV dbSNP153 33..33 33 - - - 75049 RMVar_ID_75049 Human_SNP_ID_689145851 m1A Human chr21 + 16253689 16253689 16253689 CTAACGTATTGGTCTGTTTTCGTGTTACCATAAAGATACTACCTGAGACTGGGTAATTTATAAAG CTAACGTATTGGTCTGTTTTCGTGTTACCATACAGATACTACCTGAGACTGGGTAATTTATAAAG A C MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:16253671..16253803 26863196 MeRIP-seq:(Medium) rs1010495981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2697103,Human_RBP_ID_7057246 RMVar_hsa_circ_21981,RMVar_hsa_circ_290327,RMVar_hsa_circ_349730 75050 RMVar_ID_75050 Human_SNP_ID_689182545 m1A Human chr21 - 16395146 16395146 16395146 TAACACACATAGGATCTTCTCCCTTTCCTCATATTTCTAATCTTCCCATTCCAAACCCGGACCAC TAACACACATAGGATCTTCTCCCTTTCCTCATGTTTCTAATCTTCCCATTCCAAACCCGGACCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:16395096..16395461 26863196 MeRIP-seq:(Medium) rs1443031508 Functional Loss SNV dbSNP153 33..33 33 - - - 75051 RMVar_ID_75051 Human_SNP_ID_689182834 m1A Human chr21 - 16396167 16396167 16396167 TTCCTTTACTATTCTTTTCCATCCTTCATCCCAGCCTCTCTTCGCTTTCACTTGGACTGATCCTG TTCCTTTACTATTCTTTTCCATCCTTCATCCCGGCCTCTCTTCGCTTTCACTTGGACTGATCCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:16396117..16396379 26863196 MeRIP-seq:(Medium) rs1460982180 Functional Loss SNV dbSNP153 33..33 33 - - - 75052 RMVar_ID_75052 Human_SNP_ID_689183206 m1A Human chr21 + 16397492 16397492 16397492 AGATGGGTGGGTAGAAAAGGAAGATTCAAAAGACTTAGTGACGCTTGGGGTTGGGACTGAAGGAA AGATGGGTGGGTAGAAAAGGAAGATTCAAAAGGCTTAGTGACGCTTGGGGTTGGGACTGAAGGAA A G MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:16397350..16397589 26863196 MeRIP-seq:(Medium) rs954709331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8539630 RMVar_hsa_circ_21981,RMVar_hsa_circ_349730,RMVar_hsa_circ_53998 75053 RMVar_ID_75053 Human_SNP_ID_689185799 m1A Human chr21 + 16407569 16407569 16407569 AAGGAGAGAAAAAAGGAAGGAAAGAAGGAAGAAAGGAAAAAAAGGAGGAAGGGAGGGAGGAGATA AAGGAGAGAAAAAAGGAAGGAAAGAAGGAAGATAGGAAAAAAAGGAGGAAGGGAGGGAGGAGATA A T MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:16407521..16407718 26863196 MeRIP-seq:(Medium) rs942596270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21981,RMVar_hsa_circ_349730,RMVar_hsa_circ_53998 75054 RMVar_ID_75054 Human_SNP_ID_689488663 m1A Human chr21 - 17454804 17454804 17454804 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCCATGCAGCACGAAAATGTGTTTT TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGTTTCCCGGCCCATGCAGCACGAAAATGTGTTTT T A TRG2,tRNA-Gly-GCC-1-1 RNACentral:URS00005AFD62,RNACentral:URS000063FB43 tRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1033750995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569666,Human_RBP_ID_1601873,Human_RBP_ID_8539790,Human_RBP_ID_18778173,Human_RBP_ID_20685465,Human_RBP_ID_22081844,Human_RBP_ID_22818178,Human_RBP_ID_23134004,Human_RBP_ID_24425762,Human_RBP_ID_27300474 75055 RMVar_ID_75055 Human_SNP_ID_689488664 m1A Human chr21 - 17454804 17454804 17454804 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCCATGCAGCACGAAAATGTGTTTT TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGGTTCCCGGCCCATGCAGCACGAAAATGTGTTTT T C TRG2,tRNA-Gly-GCC-1-1 RNACentral:URS00005AFD62,RNACentral:URS000063FB43 tRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1033750995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569666,Human_RBP_ID_1601873,Human_RBP_ID_8539790,Human_RBP_ID_18778173,Human_RBP_ID_20685465,Human_RBP_ID_22081844,Human_RBP_ID_22818178,Human_RBP_ID_23134004,Human_RBP_ID_24425762,Human_RBP_ID_27300474 75056 RMVar_ID_75056 Human_SNP_ID_689530804 m1A Human chr21 - 17612792 17612792 17612792 CCGGACGAGGCTCGCTGCGCTCCCTGTTGCCCAGCGCGGGCCCGTTGAGGCGGAGCCCTCAGTTC CCGGACGAGGCTCGCTGCGCTCCCTGTTGCCCCGCGCGGGCCCGTTGAGGCGGAGCCCTCAGTTC T G BTG3 Ensembl:ENSG00000154640 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:17612744..17612919 26863196 MeRIP-seq:(Medium) rs1035920623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569867,Human_RBP_ID_4679701,Human_RBP_ID_8860823,Human_RBP_ID_9299191,Human_RBP_ID_22083058 Human_Splice_Rec_2110149,Human_Splice_Rec_2110159,Human_Splice_Rec_2110171,Human_Splice_Rec_2110173 75057 RMVar_ID_75057 Human_SNP_ID_689530815 m1A Human chr21 - 17612820 17612820 17612820 CCGCCCGACGACGCGGGAGCCGCACGCGCCGGACGAGGCTCGCTGCGCTCCCTGTTGCCCAGCGC CCGCCCGACGACGCGGGAGCCGCACGCGCCGGTCGAGGCTCGCTGCGCTCCCTGTTGCCCAGCGC T A BTG3 Ensembl:ENSG00000154640 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:17612726..17612900 26863410 MeRIP-seq:(Medium) rs1331477728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245418,Human_RBP_ID_569867,Human_RBP_ID_780798,Human_RBP_ID_1601951,Human_RBP_ID_4679701,Human_RBP_ID_8860823,Human_RBP_ID_9299191,Human_RBP_ID_9391624,Human_RBP_ID_22083059 75058 RMVar_ID_75058 Human_SNP_ID_689530827 m1A Human chr21 - 17612842 17612842 17612842 AGTCCTCTCAACGCGCGCTTGGCCGCCCGACGACGCGGGAGCCGCACGCGCCGGACGAGGCTCGC AGTCCTCTCAACGCGCGCTTGGCCGCCCGACGCCGCGGGAGCCGCACGCGCCGGACGAGGCTCGC T G BTG3 Ensembl:ENSG00000154640 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr21:17612701..17612900;chr21:17612676..17612900;chr21:17612761..17612916 26863196 MeRIP-seq:(Medium) rs913547255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1305298,Human_RBP_ID_4679846,Human_RBP_ID_8860823,Human_RBP_ID_9299191,Human_RBP_ID_9391624,Human_RBP_ID_22083059 75059 RMVar_ID_75059 Human_SNP_ID_689530831 m1A Human chr21 - 17612845 17612845 17612845 GCCAGTCCTCTCAACGCGCGCTTGGCCGCCCGACGACGCGGGAGCCGCACGCGCCGGACGAGGCT GCCAGTCCTCTCAACGCGCGCTTGGCCGCCCGTCGACGCGGGAGCCGCACGCGCCGGACGAGGCT T A BTG3 Ensembl:ENSG00000154640 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr21:17612801..17612900;chr21:17612757..17612900 26863196 MeRIP-seq:(Medium) rs1361524582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1305298,Human_RBP_ID_4666486,Human_RBP_ID_8860823,Human_RBP_ID_9299191,Human_RBP_ID_9391624,Human_RBP_ID_22083059 75060 RMVar_ID_75060 Human_SNP_ID_689582311 m1A Human chr21 + 17819216 17819196 17819216 GGGGCGCCTGGCGCGCAGCAGCGCGAGGGGCCACGGGGCTCGGAACTCGAAGGAGGCGGAACGAT GGGGCGCCTGGCG____________________CGGGGCTCGGAACTCGAAGGAGGCGGAACGAT GCGCAGCAGCGCGAGGGGCCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:17819212..17819344 26863196 MeRIP-seq:(Medium) rs1285860652 Functional Loss DEL dbSNP153 14..33 33 - - - 75061 RMVar_ID_75061 Human_SNP_ID_689582340 m1A Human chr21 + 17819276 17819276 17819276 ACGATGGGACTGGGGGTCGGGGCTCAGGTGGGATGGGAGCAGGGCTGCGGGGTCTTTACCGTCCG ACGATGGGACTGGGGGTCGGGGCTCAGGTGGGCTGGGAGCAGGGCTGCGGGGTCTTTACCGTCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:17819272..17819338 26863196 MeRIP-seq:(Medium) rs1229604177 Functional Loss SNV dbSNP153 33..33 33 - - - 75062 RMVar_ID_75062 Human_SNP_ID_689840590 m1A Human chr21 + 18858004 18858004 18858004 GTGACTTCACACGCCATAATGGCACTGGTGGCAAGTCCATCTATGGGGAGAAATTTGAAGATGAG GTGACTTCACACGCCATAATGGCACTGGTGGCGAGTCCATCTATGGGGAGAAATTTGAAGATGAG A G PPIAP22 Ensembl:ENSG00000198618 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1011130151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5100712 75063 RMVar_ID_75063 Human_SNP_ID_201028232 m1A Human chr4 - 120060974 120060974 120060974 AATTAATTGATTTGATTTTTTTTTGACAGTGCACCCAGAGAAAAGTCTCAGAAAGCTATCCAGGA AATTAATTGATTTGATTTTTTTTTGACAGTGCGCCCAGAGAAAAGTCTCAGAAAGCTATCCAGGA T C MAD2L1 Ensembl:ENSG00000164109 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs778506790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_939765,Human_RBP_ID_22458711 Human_Splice_Rec_602272,Human_Splice_Rec_602278,Human_Splice_Rec_602284 RMVar_hsa_circ_95520,RMVar_hsa_circ_228319 75064 RMVar_ID_75064 Human_SNP_ID_201029617 m1A Human chr4 - 120066763 120066763 120066763 GGAGCCGCTGTGGTTGCTGTCCGCGGAGTGGAAGCGCGTGCTTTTGTTTGTGTCCCTGGCCATGG GGAGCCGCTGTGGTTGCTGTCCGCGGAGTGGAGGCGCGTGCTTTTGTTTGTGTCCCTGGCCATGG T C MAD2L1 Ensembl:ENSG00000164109 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:120066676..120066800 26863196 MeRIP-seq:(Medium) rs913007146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_612446,Human_RBP_ID_1634554,Human_RBP_ID_4771371,Human_RBP_ID_5326040,Human_RBP_ID_5475966,Human_RBP_ID_9304219,Human_RBP_ID_9334780,Human_RBP_ID_17155700,Human_RBP_ID_18424910,Human_RBP_ID_22457753,Human_RBP_ID_23213884,Human_RBP_ID_24033122,Human_RBP_ID_26771465,Human_RBP_ID_27061649 75065 RMVar_ID_75065 Human_SNP_ID_201029618 m1A Human chr4 - 120066764 120066764 120066764 TGGAGCCGCTGTGGTTGCTGTCCGCGGAGTGGAAGCGCGTGCTTTTGTTTGTGTCCCTGGCCATG TGGAGCCGCTGTGGTTGCTGTCCGCGGAGTGGGAGCGCGTGCTTTTGTTTGTGTCCCTGGCCATG T C MAD2L1 Ensembl:ENSG00000164109 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:120066703..120066825 26863196 MeRIP-seq:(Medium) rs750202365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_612446,Human_RBP_ID_1634554,Human_RBP_ID_4771371,Human_RBP_ID_5326040,Human_RBP_ID_5475966,Human_RBP_ID_9304219,Human_RBP_ID_9334780,Human_RBP_ID_17155700,Human_RBP_ID_18424910,Human_RBP_ID_22457753,Human_RBP_ID_23213884,Human_RBP_ID_24033122,Human_RBP_ID_26771465,Human_RBP_ID_27061649 75066 RMVar_ID_75066 Human_SNP_ID_201073904 m1A Human chr4 + 120256618 120256618 120256618 GAGGCAATGCCTCGCCCTGCTTCTGCTCGCGCACGGTGCACGCACCCACTGACCTGCGCCCACTG GAGGCAATGCCTCGCCCTGCTTCTGCTCGCGCGCGGTGCACGCACCCACTGACCTGCGCCCACTG A G AC073475.1 Ensembl:ENSG00000250938 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:120256569..120256656 26863410 MeRIP-seq:(Medium) rs941145949 Functional Loss SNV dbSNP153 33..33 33 - - - 75067 RMVar_ID_75067 Human_SNP_ID_201422347 m1A Human chr4 - 121677952 121677952 121677952 ATAGTTCAGTAATGTGACATATTACCTCTCATAGGCTAACAGAGACCCTGATGCTGGAATTGATG ATAGTTCAGTAATGTGACATATTACCTCTCATCGGCTAACAGAGACCCTGATGCTGGAATTGATG T G ANXA5 Ensembl:ENSG00000164111 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:121672526..121678001 32194978 MeRIP-seq:(Medium) rs1453480297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71972,Human_RBP_ID_22552657 Human_Splice_Rec_602671,Human_Splice_Rec_602691,Human_Splice_Rec_602715,Human_Splice_Rec_602733,Human_Splice_Rec_602743,Human_Splice_Rec_602771 RMVar_hsa_circ_22446,RMVar_hsa_circ_24234,RMVar_hsa_circ_228342,RMVar_hsa_circ_353731,RMVar_hsa_circ_32261,RMVar_hsa_circ_269297,RMVar_hsa_circ_335903 75068 RMVar_ID_75068 Human_SNP_ID_201422457 m1A Human chr4 - 121678403 121678403 121678403 ATGTTGGTGGTTCTCCTTCAGGTATTGCGTGGAGATTAATTACAGTTTGATTAAAAAGCCTGAAG ATGTTGGTGGTTCTCCTTCAGGTATTGCGTGGGGATTAATTACAGTTTGATTAAAAAGCCTGAAG T C ANXA5 Ensembl:ENSG00000164111 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:121678401..121681395 32194978 MeRIP-seq:(Medium) rs760027157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2815545 Human_Splice_Rec_602668,Human_Splice_Rec_602688,Human_Splice_Rec_602712,Human_Splice_Rec_602713,Human_Splice_Rec_602730,Human_Splice_Rec_602768,Human_Splice_Rec_602784 Human_miRNA_ID_613250 RMVar_hsa_circ_22446,RMVar_hsa_circ_24234,RMVar_hsa_circ_228342,RMVar_hsa_circ_353731,RMVar_hsa_circ_32261,RMVar_hsa_circ_269297,RMVar_hsa_circ_335903 75069 RMVar_ID_75069 Human_SNP_ID_201422678 m1A Human chr4 + 121679304 121679304 121679304 TTCTACACCAACACCTGTAAATATTAACCATTAAATCCTATCACGTTTCTCCTGTCCCTGATTTA TTCTACACCAACACCTGTAAATATTAACCATTGAATCCTATCACGTTTCTCCTGTCCCTGATTTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:121679301..121679692 26863196 MeRIP-seq:(Medium) rs954774753 Functional Loss SNV dbSNP153 33..33 33 - - - 75070 RMVar_ID_75070 Human_SNP_ID_201423924 m1A Human chr4 - 121684773 121684773 121684773 GAGCCAAAATGTAATTGTTAACCATAAATTGCAGGCACAGATGAGGAGAGCATCCTGACTCTGTT GAGCCAAAATGTAATTGTTAACCATAAATTGCTGGCACAGATGAGGAGAGCATCCTGACTCTGTT T A ANXA5 Ensembl:ENSG00000164111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:121684757..121684828 26863196 MeRIP-seq:(Medium) rs773203351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4796824,Human_RBP_ID_22457982,Human_RBP_ID_22679988 Human_Splice_Rec_602663,Human_Splice_Rec_602707,Human_Splice_Rec_602763,Human_Splice_Rec_602779,Human_Splice_Rec_602791 RMVar_hsa_circ_116367,RMVar_hsa_circ_335903,RMVar_hsa_circ_326984,RMVar_hsa_circ_228343,RMVar_hsa_circ_50803 75071 RMVar_ID_75071 Human_SNP_ID_201423925 m1A Human chr4 - 121684773 121684773 121684773 GAGCCAAAATGTAATTGTTAACCATAAATTGCAGGCACAGATGAGGAGAGCATCCTGACTCTGTT GAGCCAAAATGTAATTGTTAACCATAAATTGCGGGCACAGATGAGGAGAGCATCCTGACTCTGTT T C ANXA5 Ensembl:ENSG00000164111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:121684757..121684828 26863196 MeRIP-seq:(Medium) rs773203351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4796824,Human_RBP_ID_22457982,Human_RBP_ID_22679988 Human_Splice_Rec_602663,Human_Splice_Rec_602707,Human_Splice_Rec_602763,Human_Splice_Rec_602779,Human_Splice_Rec_602791 RMVar_hsa_circ_116367,RMVar_hsa_circ_335903,RMVar_hsa_circ_326984,RMVar_hsa_circ_228343,RMVar_hsa_circ_50803 75072 RMVar_ID_75072 Human_SNP_ID_201426911 m1A Human chr4 + 121696621 121696621 121696621 TGGCGACTACTCAGGTCAGGGGAAGGTGAAGCAGGACTGCAAAAGAGAAGAAACCTCGGGCTTAG TGGCGACTACTCAGGTCAGGGGAAGGTGAAGCCGGACTGCAAAAGAGAAGAAACCTCGGGCTTAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:121696576..121696625 32194978 MeRIP-seq:(Medium) rs924094198 Functional Loss SNV dbSNP153 33..33 33 - - - 75073 RMVar_ID_75073 Human_SNP_ID_201451274 m1A Human chr4 + 121801434 121801434 121801434 TGTGGGGCCGGTGACCCAACACCATGAAGGAAACGCCACTCTCAAACTGCGAACGCCGCTTCCTA TGTGGGGCCGGTGACCCAACACCATGAAGGAAGCGCCACTCTCAAACTGCGAACGCCGCTTCCTA A G EXOSC9 Ensembl:ENSG00000123737 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:121801384..121801463 26863196 MeRIP-seq:(Medium) rs1166219167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1634654,Human_RBP_ID_4795112,Human_RBP_ID_18424633,Human_RBP_ID_26825597 Human_Splice_Rec_602885,Human_Splice_Rec_602905,Human_Splice_Rec_602929,Human_Splice_Rec_602951,Human_Splice_Rec_602971,Human_Splice_Rec_602983 75074 RMVar_ID_75074 Human_SNP_ID_201454621 m1A Human chr4 - 121814016 121814015 121814017 CCTTGGCTTCCAATATCAGAGACTTCTACTCCAGTGTCCATTTTTATACCATCAAGAATGATAGC CCTTGGCTTCCAATATCAGAGACTTCTACTC__GTGTCCATTTTTATACCATCAAGAATGATAGC CTG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:121811587..121814069 32194978 MeRIP-seq:(Medium) rs1267604674 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3727426 75075 RMVar_ID_75075 Human_SNP_ID_201455878 m1A Human chr4 + 121818136 121818136 121818136 GTCTGGTGAAGGTCCATGAGACAAGGCTTAAGACTTTCCAGGGTATATCCAGTCTTTCGTATTAA GTCTGGTGAAGGTCCATGAGACAAGGCTTAAGCCTTTCCAGGGTATATCCAGTCTTTCGTATTAA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:121818101..121818150 26863196 MeRIP-seq:(Medium) rs1179916851 Functional Loss SNV dbSNP153 33..33 33 - - - 75076 RMVar_ID_75076 Human_SNP_ID_201457169 m1A Human chr4 - 121823435 121823435 121823435 GTCCGGGAACCCGCGGGGTCTAGCGCAGCAGCAGAGGCCGAAGACGAGACGGGTAAAGGGATGCG GTCCGGGAACCCGCGGGGTCTAGCGCAGCAGCGGAGGCCGAAGACGAGACGGGTAAAGGGATGCG T C CCNA2 Ensembl:ENSG00000145386 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:121822476..121823434 32194978 MeRIP-seq:(Medium) rs746929651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_612632,Human_RBP_ID_22095640 Human_Splice_Rec_603053,Human_Splice_Rec_603067 75077 RMVar_ID_75077 Human_SNP_ID_201534245 m1A Human chr4 - 122152495 122152495 122152495 GGGCCTTGGGCGGCGGCAGGGGCGGCGACGGCAGCAGCACCGAGCCGGATGCAGCCTGCGAAGCT GGGCCTTGGGCGGCGGCAGGGGCGGCGACGGCGGCAGCACCGAGCCGGATGCAGCCTGCGAAGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:122152447..122152536 26863196 MeRIP-seq:(Medium) rs1450378823 Functional Loss SNV dbSNP153 33..33 33 - - - 75078 RMVar_ID_75078 Human_SNP_ID_201692939 m1A Human chr4 + 122827093 122827057 122827093 CGGGGCCGGGGCCGTGCCCCGGAGCGGGTCGGAGGCCGGGGCCGGGGCCGGGGGACGGCGGCTCC _________________________________GGCCGGGGCCGGGGCCGGGGGACGGCGGCTCC GGGCCGGGGCCGGGGCCGTGCCCCGGAGCGGGTCGGA G FGF2 Ensembl:ENSG00000138685 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:122826695..122827376 26863196 MeRIP-seq:(Medium) rs1317199402 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_5326041 RMVar_hsa_circ_228428,RMVar_hsa_circ_126202 75079 RMVar_ID_75079 Human_SNP_ID_201692944 m1A Human chr4 + 122827093 122827063 122827093 CGGGGCCGGGGCCGTGCCCCGGAGCGGGTCGGAGGCCGGGGCCGGGGCCGGGGGACGGCGGCTCC CGG______________________________GGCCGGGGCCGGGGCCGGGGGACGGCGGCTCC GGGCCGGGGCCGTGCCCCGGAGCGGGTCGGA G FGF2 Ensembl:ENSG00000138685 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:122826695..122827376 26863196 MeRIP-seq:(Medium) rs1227851575 Functional Loss DEL dbSNP153 4..33 33 - - - Human_RBP_ID_5326041 RMVar_hsa_circ_228428,RMVar_hsa_circ_126202 75080 RMVar_ID_75080 Human_SNP_ID_201692957 m1A Human chr4 - 122827089 122827089 122827089 CCGCCGTCCCCCGGCCCCGGCCCCGGCCTCCGACCCGCTCCGGGGCACGGCCCCGGCCCCGGCCC CCGCCGTCCCCCGGCCCCGGCCCCGGCCTCCGTCCCGCTCCGGGGCACGGCCCCGGCCCCGGCCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:122826863..122827256 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 75081 RMVar_ID_75081 Human_SNP_ID_201692958 m1A Human chr4 - 122827089 122827089 122827089 CCGCCGTCCCCCGGCCCCGGCCCCGGCCTCCGACCCGCTCCGGGGCACGGCCCCGGCCCCGGCCC CCGCCGTCCCCCGGCCCCGGCCCCGGCCTCCGGCCCGCTCCGGGGCACGGCCCCGGCCCCGGCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:122826863..122827256 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 75082 RMVar_ID_75082 Human_SNP_ID_201704348 m1A Human chr4 - 122876277 122876277 122876277 AAAAAAATTATCTTTGTAGCACCACAGAGGAAAGAGCCTTCTTCACAATATTTACGCAATATAAA AAAAAAATTATCTTTGTAGCACCACAGAGGAACGAGCCTTCTTCACAATATTTACGCAATATAAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122876274..122876347 26863196 MeRIP-seq:(Medium) rs1472297948 Functional Loss SNV dbSNP153 33..33 33 - - - 75083 RMVar_ID_75083 Human_SNP_ID_201713562 m1A Human chr4 - 122917736 122917736 122917736 TGAGTTTTAATTTATTCCACTCGTCTCTTTGGAAATTATTTAGACTTTTTTCTTCTGCATTTAGC TGAGTTTTAATTTATTCCACTCGTCTCTTTGGTAATTATTTAGACTTTTTTCTTCTGCATTTAGC T A NUDT6 Ensembl:ENSG00000170917 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:122917693..122917793 26863196 MeRIP-seq:(Medium) rs1053434949 Functional Loss SNV dbSNP153 33..33 33 - - - 75084 RMVar_ID_75084 Human_SNP_ID_201714786 m1A Human chr4 - 122922561 122922554 122922562 GACGAATTAAGCGGCGTGGAGATGCGGCAGCCACTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC GACGAATTAAGCGGCGTGGAGATGCGGCAGC________TGGGGCCGCTGGCGCGCGATGCTTGC AGCTCAGTG A NUDT6 Ensembl:ENSG00000170917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122922362..122922577 26863196 MeRIP-seq:(Medium) rs769058797 Functional Loss DEL dbSNP153 32..39 33 - - - 75085 RMVar_ID_75085 Human_SNP_ID_201714796 m1A Human chr4 - 122922561 122922561 122922561 GACGAATTAAGCGGCGTGGAGATGCGGCAGCCACTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC GACGAATTAAGCGGCGTGGAGATGCGGCAGCCTCTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC T A NUDT6 Ensembl:ENSG00000170917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122922362..122922577 26863196 MeRIP-seq:(Medium) rs13134412 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_9074,GWAS_ID_9075,GWAS_ID_9076 75086 RMVar_ID_75086 Human_SNP_ID_201714797 m1A Human chr4 - 122922561 122922561 122922561 GACGAATTAAGCGGCGTGGAGATGCGGCAGCCACTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC GACGAATTAAGCGGCGTGGAGATGCGGCAGCCGCTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC T C NUDT6 Ensembl:ENSG00000170917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122922362..122922577 26863196 MeRIP-seq:(Medium) rs13134412 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_9074,GWAS_ID_9075,GWAS_ID_9076 75087 RMVar_ID_75087 Human_SNP_ID_201714798 m1A Human chr4 - 122922561 122922561 122922561 GACGAATTAAGCGGCGTGGAGATGCGGCAGCCACTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC GACGAATTAAGCGGCGTGGAGATGCGGCAGCCCCTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC T G NUDT6 Ensembl:ENSG00000170917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122922362..122922577 26863196 MeRIP-seq:(Medium) rs13134412 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9074,GWAS_ID_9075,GWAS_ID_9076 75088 RMVar_ID_75088 Human_SNP_ID_201715085 m1A Human chr4 - 122923206 122923206 122923206 AGCCCGTGCCTCCGCACAAGAGGAAGCAGCAGAGGGCAAGGACGAACCATTTTCCGCGCTTTGGT AGCCCGTGCCTCCGCACAAGAGGAAGCAGCAGCGGGCAAGGACGAACCATTTTCCGCGCTTTGGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122923156..122923247 26863196 MeRIP-seq:(Medium) rs1395411329 Functional Loss SNV dbSNP153 33..33 33 - - - 75089 RMVar_ID_75089 Human_SNP_ID_201736922 m1A Human chr4 - 123011805 123011805 123011805 TTCACTCTGTCTCTACCCTCTCTTTTCTCTGGACTTGCTCCTTCACTATAGGCAACCTTCCACCC TTCACTCTGTCTCTACCCTCTCTTTTCTCTGGTCTTGCTCCTTCACTATAGGCAACCTTCCACCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:123011798..123011913 26863196 MeRIP-seq:(Medium) rs1389727432 Functional Loss SNV dbSNP153 33..33 33 - - - 75090 RMVar_ID_75090 Human_SNP_ID_202140319 m1A Human chr4 + 124712652 124712652 124712652 CCTCCTCTTGGCCCCCGGCGGCTGCCAGTTCCAGCTTTCCCAGCAGAATCGGTCGTGCTCGCCCC CCTCCTCTTGGCCCCCGGCGGCTGCCAGTTCCGGCTTTCCCAGCAGAATCGGTCGTGCTCGCCCC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:124712623..124712708 26863410 MeRIP-seq:(Medium) rs1288397631 Functional Loss SNV dbSNP153 33..33 33 - - - 75091 RMVar_ID_75091 Human_SNP_ID_202291270 m1A Human chr4 - 125315012 125315012 125315012 GAAACACAAACAGAGGGGGAGGGAAGACCGCGAGCTGGAGCAGCACTCAGAAACTTTGCTCGACA GAAACACAAACAGAGGGGGAGGGAAGACCGCGGGCTGGAGCAGCACTCAGAAACTTTGCTCGACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:125314983..125315166 26863196 MeRIP-seq:(Medium) rs1432062754 Functional Loss SNV dbSNP153 33..33 33 - - - 75092 RMVar_ID_75092 Human_SNP_ID_202291391 m1A Human chr4 - 125315281 125315281 125315281 GATGCCTCTCTCTCCTTCACAGTTGGCAGCGGAGGCGGCGAAGTCGGCGCTGGGCTGTAGTGACG GATGCCTCTCTCTCCTTCACAGTTGGCAGCGGCGGCGGCGAAGTCGGCGCTGGGCTGTAGTGACG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:125315235..125315361 26863196 MeRIP-seq:(Medium) rs1246060153 Functional Loss SNV dbSNP153 33..33 33 - - - 75093 RMVar_ID_75093 Human_SNP_ID_202894991 m1A Human chr4 - 127782401 127782401 127782401 CCAAGTCGCTAAGCAGAAAATCTAGGGCAGGGAGTCGGAAACCCGCGGAAGGAGCAGAGGCCGTC CCAAGTCGCTAAGCAGAAAATCTAGGGCAGGGCGTCGGAAACCCGCGGAAGGAGCAGAGGCCGTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127782350..127782436 26863196 MeRIP-seq:(Medium) rs925732914 Functional Loss SNV dbSNP153 33..33 33 - - - 75094 RMVar_ID_75094 Human_SNP_ID_202917751 m1A Human chr4 + 127880960 127880960 127880960 ATTTTCAAAATGGGAGCCCAGAGGCACCGCCCAGGCCTCGGAAGGTGTCAGGGAGAACTTTCCGT ATTTTCAAAATGGGAGCCCAGAGGCACCGCCCGGGCCTCGGAAGGTGTCAGGGAGAACTTTCCGT A G PLK4 Ensembl:ENSG00000142731 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:127880901..127881233 26863196 MeRIP-seq:(Medium) rs986055505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4772659,Human_RBP_ID_18424635,Human_RBP_ID_22095650,Human_RBP_ID_26350277 RMVar_hsa_circ_105749,RMVar_hsa_circ_228513 75095 RMVar_ID_75095 Human_SNP_ID_202917759 m1A Human chr4 + 127880977 127880977 127880977 CCAGAGGCACCGCCCAGGCCTCGGAAGGTGTCAGGGAGAACTTTCCGTGGTTTCAGCGTCGTCGC CCAGAGGCACCGCCCAGGCCTCGGAAGGTGTCTGGGAGAACTTTCCGTGGTTTCAGCGTCGTCGC A T PLK4 Ensembl:ENSG00000142731 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:127880926..127881213;chr4:127880926..127881082 26863196 MeRIP-seq:(Medium) rs1327712415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795626,Human_RBP_ID_18424635 Human_miRNA_ID_3000798 RMVar_hsa_circ_105749,RMVar_hsa_circ_228513 75096 RMVar_ID_75096 Human_SNP_ID_202917764 m1A Human chr4 + 127880999 127880999 127880999 GGAAGGTGTCAGGGAGAACTTTCCGTGGTTTCAGCGTCGTCGCCTGGAGCGGCGGTTTAGAGAGC GGAAGGTGTCAGGGAGAACTTTCCGTGGTTTCGGCGTCGTCGCCTGGAGCGGCGGTTTAGAGAGC A G PLK4 Ensembl:ENSG00000142731 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:127880948..127881110 26863196 MeRIP-seq:(Medium) rs897209984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795626,Human_RBP_ID_9396669 RMVar_hsa_circ_105749,RMVar_hsa_circ_228513 75097 RMVar_ID_75097 Human_SNP_ID_202917768 m1A Human chr4 - 127881011 127881011 127881011 CCATCAGGCTCGGCTCTCTAAACCGCCGCTCCAGGCGACGACGCTGAAACCACGGAAAGTTCTCC CCATCAGGCTCGGCTCTCTAAACCGCCGCTCCCGGCGACGACGCTGAAACCACGGAAAGTTCTCC T G lnc-MFSD8-12,lnc-MFSD8-12:2 RNACentral:URS0000D5D4FC,RNACentral:URS0000D5899F lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:127880961..127881087 26863196 MeRIP-seq:(Medium) rs773608097 Functional Loss SNV dbSNP153 33..33 33 - - - 75098 RMVar_ID_75098 Human_SNP_ID_202937284 m1A Human chr4 - 127957589 127957589 127957589 TATACTACTTTTTTCTTCTTTACACCTAGAGAATGGGACATTTTAGAGACTGAAGAGCATTATAA TATACTACTTTTTTCTTCTTTACACCTAGAGATTGGGACATTTTAGAGACTGAAGAGCATTATAA T A MFSD8 Ensembl:ENSG00000164073 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:127957582..127957653 26863196 MeRIP-seq:(Medium) rs145529594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7266506,Human_RBP_ID_15042681,Human_RBP_ID_24034755,Human_RBP_ID_25829527 Human_Splice_Rec_605292,Human_Splice_Rec_605293,Human_Splice_Rec_605318,Human_Splice_Rec_605319,Human_Splice_Rec_605340,Human_Splice_Rec_605341,Human_Splice_Rec_605360,Human_Splice_Rec_605361,Human_Splice_Rec_605378,Human_Splice_Rec_605379,Human_Splice_Rec_605398,Human_Splice_Rec_605399,Human_Splice_Rec_605422,Human_Splice_Rec_605423,Human_Splice_Rec_605440,Human_Splice_Rec_605441,Human_Splice_Rec_605456,Human_Splice_Rec_605457,Human_Splice_Rec_605474,Human_Splice_Rec_605475,Human_Splice_Rec_605490,Human_Splice_Rec_605491,Human_Splice_Rec_605504,Human_Splice_Rec_605505,Human_Splice_Rec_605524,Human_Splice_Rec_605525,Human_Splice_Rec_605540,Human_Splice_Rec_605541,Human_Splice_Rec_605556,Human_Splice_Rec_605557,Human_Splice_Rec_605574,Human_Splice_Rec_605575,Human_Splice_Rec_605596,Human_Splice_Rec_605597,Human_Splice_Rec_605612,Human_Splice_Rec_605613,Human_Splice_Rec_605634,Human_Splice_Rec_605635,Human_Splice_Rec_605658,Human_Splice_Rec_605659,Human_Splice_Rec_605676,Human_Splice_Rec_605677,Human_Splice_Rec_605726,Human_Splice_Rec_605727,Human_Splice_Rec_605746,Human_Splice_Rec_605747,Human_Splice_Rec_605766,Human_Splice_Rec_605767,Human_Splice_Rec_605784,Human_Splice_Rec_605785,Human_Splice_Rec_605794,Human_Splice_Rec_605795,Human_Splice_Rec_605808,Human_Splice_Rec_605809,Human_Splice_Rec_605824,Human_Splice_Rec_605825,Human_Splice_Rec_605840,Human_Splice_Rec_605841,Human_Splice_Rec_605858,Human_Splice_Rec_605859,Human_Splice_Rec_605876,Human_Splice_Rec_605877,Human_Splice_Rec_605896,Human_Splice_Rec_605897,Human_Splice_Rec_605916,Human_Splice_Rec_605917,Human_Splice_Rec_605946,Human_Splice_Rec_605947,Human_Splice_Rec_605964,Human_Splice_Rec_605965,Human_Splice_Rec_605984,Human_Splice_Rec_605985,Human_Splice_Rec_606041,Human_Splice_Rec_606044,Human_Splice_Rec_606045,Human_Splice_Rec_606056,Human_Splice_Rec_606057,Human_Splice_Rec_606070,Human_Splice_Rec_606071,Human_Splice_Rec_606082,Human_Splice_Rec_606083,Human_Splice_Rec_606096,Human_Splice_Rec_606097,Human_Splice_Rec_606108,Human_Splice_Rec_606109,Human_Splice_Rec_606122,Human_Splice_Rec_606123,Human_Splice_Rec_606134,Human_Splice_Rec_606135,Human_Splice_Rec_606152,Human_Splice_Rec_606153,Human_Splice_Rec_606162,Human_Splice_Rec_606163,Human_Splice_Rec_606170,Human_Splice_Rec_606171,Human_Splice_Rec_606178,Human_Splice_Rec_606179,Human_Splice_Rec_606184,Human_Splice_Rec_606185 Clinvar_Rec_344 RMVar_hsa_circ_87611,RMVar_hsa_circ_228522,RMVar_hsa_circ_56324,RMVar_hsa_circ_23559,RMVar_hsa_circ_95675,RMVar_hsa_circ_264921,RMVar_hsa_circ_358815,RMVar_hsa_circ_228534,RMVar_hsa_circ_228535,RMVar_hsa_circ_79581,RMVar_hsa_circ_228536 75099 RMVar_ID_75099 Human_SNP_ID_202937285 m1A Human chr4 - 127957589 127957589 127957589 TATACTACTTTTTTCTTCTTTACACCTAGAGAATGGGACATTTTAGAGACTGAAGAGCATTATAA TATACTACTTTTTTCTTCTTTACACCTAGAGAGTGGGACATTTTAGAGACTGAAGAGCATTATAA T C MFSD8 Ensembl:ENSG00000164073 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:127957582..127957653 26863196 MeRIP-seq:(Medium) rs145529594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7266506,Human_RBP_ID_15042681,Human_RBP_ID_24034755,Human_RBP_ID_25829527 Human_Splice_Rec_605292,Human_Splice_Rec_605293,Human_Splice_Rec_605318,Human_Splice_Rec_605319,Human_Splice_Rec_605340,Human_Splice_Rec_605341,Human_Splice_Rec_605360,Human_Splice_Rec_605361,Human_Splice_Rec_605378,Human_Splice_Rec_605379,Human_Splice_Rec_605398,Human_Splice_Rec_605399,Human_Splice_Rec_605422,Human_Splice_Rec_605423,Human_Splice_Rec_605440,Human_Splice_Rec_605441,Human_Splice_Rec_605456,Human_Splice_Rec_605457,Human_Splice_Rec_605474,Human_Splice_Rec_605475,Human_Splice_Rec_605490,Human_Splice_Rec_605491,Human_Splice_Rec_605504,Human_Splice_Rec_605505,Human_Splice_Rec_605524,Human_Splice_Rec_605525,Human_Splice_Rec_605540,Human_Splice_Rec_605541,Human_Splice_Rec_605556,Human_Splice_Rec_605557,Human_Splice_Rec_605574,Human_Splice_Rec_605575,Human_Splice_Rec_605596,Human_Splice_Rec_605597,Human_Splice_Rec_605612,Human_Splice_Rec_605613,Human_Splice_Rec_605634,Human_Splice_Rec_605635,Human_Splice_Rec_605658,Human_Splice_Rec_605659,Human_Splice_Rec_605676,Human_Splice_Rec_605677,Human_Splice_Rec_605726,Human_Splice_Rec_605727,Human_Splice_Rec_605746,Human_Splice_Rec_605747,Human_Splice_Rec_605766,Human_Splice_Rec_605767,Human_Splice_Rec_605784,Human_Splice_Rec_605785,Human_Splice_Rec_605794,Human_Splice_Rec_605795,Human_Splice_Rec_605808,Human_Splice_Rec_605809,Human_Splice_Rec_605824,Human_Splice_Rec_605825,Human_Splice_Rec_605840,Human_Splice_Rec_605841,Human_Splice_Rec_605858,Human_Splice_Rec_605859,Human_Splice_Rec_605876,Human_Splice_Rec_605877,Human_Splice_Rec_605896,Human_Splice_Rec_605897,Human_Splice_Rec_605916,Human_Splice_Rec_605917,Human_Splice_Rec_605946,Human_Splice_Rec_605947,Human_Splice_Rec_605964,Human_Splice_Rec_605965,Human_Splice_Rec_605984,Human_Splice_Rec_605985,Human_Splice_Rec_606041,Human_Splice_Rec_606044,Human_Splice_Rec_606045,Human_Splice_Rec_606056,Human_Splice_Rec_606057,Human_Splice_Rec_606070,Human_Splice_Rec_606071,Human_Splice_Rec_606082,Human_Splice_Rec_606083,Human_Splice_Rec_606096,Human_Splice_Rec_606097,Human_Splice_Rec_606108,Human_Splice_Rec_606109,Human_Splice_Rec_606122,Human_Splice_Rec_606123,Human_Splice_Rec_606134,Human_Splice_Rec_606135,Human_Splice_Rec_606152,Human_Splice_Rec_606153,Human_Splice_Rec_606162,Human_Splice_Rec_606163,Human_Splice_Rec_606170,Human_Splice_Rec_606171,Human_Splice_Rec_606178,Human_Splice_Rec_606179,Human_Splice_Rec_606184,Human_Splice_Rec_606185 Clinvar_Rec_344 RMVar_hsa_circ_87611,RMVar_hsa_circ_228522,RMVar_hsa_circ_56324,RMVar_hsa_circ_23559,RMVar_hsa_circ_95675,RMVar_hsa_circ_264921,RMVar_hsa_circ_358815,RMVar_hsa_circ_228534,RMVar_hsa_circ_228535,RMVar_hsa_circ_79581,RMVar_hsa_circ_228536 75100 RMVar_ID_75100 Human_SNP_ID_202938612 m1A Human chr4 - 127963375 127963375 127963375 ACCAAGAACCCACCAATCCCGGACACAAAGCCACCACATTCTGTATCTTCTGCATTCCATATTTG ACCAAGAACCCACCAATCCCGGACACAAAGCCGCCACATTCTGTATCTTCTGCATTCCATATTTG T C MFSD8 Ensembl:ENSG00000164073 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127963373..127963518 26863196 MeRIP-seq:(Medium) rs1483083828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95675,RMVar_hsa_circ_264921,RMVar_hsa_circ_228535,RMVar_hsa_circ_79581,RMVar_hsa_circ_228536 75101 RMVar_ID_75101 Human_SNP_ID_202939142 m1A Human chr4 - 127965092 127965092 127965092 CTGCGGAACGAAAGTGAACAGGAGCCGCTCTTAGGCGACACACCTGGAAGCAGGTGAGCGGATCC CTGCGGAACGAAAGTGAACAGGAGCCGCTCTTGGGCGACACACCTGGAAGCAGGTGAGCGGATCC T C MFSD8 Ensembl:ENSG00000164073 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:127965063..127965154 26863196 MeRIP-seq:(Medium) rs1160479250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9397435,Human_RBP_ID_18424636,Human_RBP_ID_19014583 Human_Splice_Rec_605291,Human_Splice_Rec_605317,Human_Splice_Rec_605339,Human_Splice_Rec_605359,Human_Splice_Rec_605377,Human_Splice_Rec_605397,Human_Splice_Rec_605421,Human_Splice_Rec_605473,Human_Splice_Rec_605489,Human_Splice_Rec_605503,Human_Splice_Rec_605523,Human_Splice_Rec_605555,Human_Splice_Rec_605573,Human_Splice_Rec_605633,Human_Splice_Rec_605657,Human_Splice_Rec_605675,Human_Splice_Rec_605725,Human_Splice_Rec_605745,Human_Splice_Rec_605765,Human_Splice_Rec_605783,Human_Splice_Rec_605793,Human_Splice_Rec_605807,Human_Splice_Rec_605839,Human_Splice_Rec_605857,Human_Splice_Rec_605875,Human_Splice_Rec_605915,Human_Splice_Rec_605945,Human_Splice_Rec_605963,Human_Splice_Rec_605983,Human_Splice_Rec_606031,Human_Splice_Rec_606043,Human_Splice_Rec_606081,Human_Splice_Rec_606095,Human_Splice_Rec_606107,Human_Splice_Rec_606121,Human_Splice_Rec_606133,Human_Splice_Rec_606151,Human_Splice_Rec_606161,Human_Splice_Rec_606169,Human_Splice_Rec_606177 RMVar_hsa_circ_95675,RMVar_hsa_circ_264921,RMVar_hsa_circ_228535,RMVar_hsa_circ_79581,RMVar_hsa_circ_228536 75102 RMVar_ID_75102 Human_SNP_ID_202939333 m1A Human chr4 - 127965525 127965521 127965526 CGCCGCTCTCCAGGCTCCCTTTCCAGGACTCAACTTTGGTCCCAGCCCCAATCGCAGCTCCGGTA CGCCGCTCTCCAGGCTCCCTTTCCAGGACTC_____TGGTCCCAGCCCCAATCGCAGCTCCGGTA AAAGTT A MFSD8 Ensembl:ENSG00000164073 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127965450..127965573 26863196 MeRIP-seq:(Medium) rs1480287180 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_95675,RMVar_hsa_circ_228535 75103 RMVar_ID_75103 Human_SNP_ID_202939334 m1A Human chr4 - 127965525 127965525 127965525 CGCCGCTCTCCAGGCTCCCTTTCCAGGACTCAACTTTGGTCCCAGCCCCAATCGCAGCTCCGGTA CGCCGCTCTCCAGGCTCCCTTTCCAGGACTCAGCTTTGGTCCCAGCCCCAATCGCAGCTCCGGTA T C MFSD8 Ensembl:ENSG00000164073 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127965450..127965573 26863196 MeRIP-seq:(Medium) rs987492661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95675,RMVar_hsa_circ_228535 75104 RMVar_ID_75104 Human_SNP_ID_202939406 m1A Human chr4 + 127965718 127965718 127965718 GCAGGGACCGGGGACGCGGAGCTGGGCGGGAGACTCGCGGGTCAGGGACGCGGGGTGAGGCTGGG GCAGGGACCGGGGACGCGGAGCTGGGCGGGAGGCTCGCGGGTCAGGGACGCGGGGTGAGGCTGGG A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127965711..127965802 26863196 MeRIP-seq:(Medium) rs1182123211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211782,Human_RBP_ID_26791667 75105 RMVar_ID_75105 Human_SNP_ID_202939407 m1A Human chr4 + 127965718 127965718 127965718 GCAGGGACCGGGGACGCGGAGCTGGGCGGGAGACTCGCGGGTCAGGGACGCGGGGTGAGGCTGGG GCAGGGACCGGGGACGCGGAGCTGGGCGGGAGTCTCGCGGGTCAGGGACGCGGGGTGAGGCTGGG A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:127965711..127965802 26863196 MeRIP-seq:(Medium) rs1182123211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211782,Human_RBP_ID_26791667 75106 RMVar_ID_75106 Human_SNP_ID_202963710 m1A Human chr4 + 128062052 128062052 128062052 GCCGCCGTCGCCGTTGCCGCCGTTGCTGCGGGATCCGCCGGCCGAGGACGCCCGGGAAGAGGTGG GCCGCCGTCGCCGTTGCCGCCGTTGCTGCGGGTTCCGCCGGCCGAGGACGCCCGGGAAGAGGTGG A T LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:128061676..128062241 26863196 MeRIP-seq:(Medium) rs1560993926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5210912,Human_RBP_ID_5242136,Human_RBP_ID_5326045,Human_RBP_ID_5394883,Human_RBP_ID_8212436,Human_RBP_ID_8730019,Human_RBP_ID_8943763,Human_RBP_ID_9334792,Human_RBP_ID_18501034,Human_RBP_ID_22287768 RMVar_hsa_circ_228558,RMVar_hsa_circ_102311 75107 RMVar_ID_75107 Human_SNP_ID_202972430 m1A Human chr4 + 128091087 128091075 128091087 GAAGTGAGGGTGGTAATATCCGAGGTTCCTTTAGAGGTCGAGGAAGAGGCCGAGGACGGGGAAGA GAAGTGAGGGTGGTAATATCC____________GAGGTCGAGGAAGAGGCCGAGGACGGGGAAGA CGAGGTTCCTTTA C LARP1B Ensembl:ENSG00000138709 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:128077866..128091131 26863196 MeRIP-seq:(Medium) rs769677529 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5507355,Human_RBP_ID_9396678 Human_Splice_Rec_606314,Human_Splice_Rec_606315,Human_Splice_Rec_606334,Human_Splice_Rec_606335,Human_Splice_Rec_606360,Human_Splice_Rec_606361,Human_Splice_Rec_606398,Human_Splice_Rec_606399,Human_Splice_Rec_606416,Human_Splice_Rec_606417,Human_Splice_Rec_606432,Human_Splice_Rec_606433,Human_Splice_Rec_606470,Human_Splice_Rec_606471,Human_Splice_Rec_606488,Human_Splice_Rec_606489,Human_Splice_Rec_606498,Human_Splice_Rec_606499 RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_228558,RMVar_hsa_circ_102311,RMVar_hsa_circ_329939,RMVar_hsa_circ_360511,RMVar_hsa_circ_286422,RMVar_hsa_circ_291803,RMVar_hsa_circ_281172,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228565,RMVar_hsa_circ_228566,RMVar_hsa_circ_228563,RMVar_hsa_circ_228564,RMVar_hsa_circ_228562,RMVar_hsa_circ_348078,RMVar_hsa_circ_228559,RMVar_hsa_circ_228560,RMVar_hsa_circ_358732,RMVar_hsa_circ_349074,RMVar_hsa_circ_62080,RMVar_hsa_circ_360384,RMVar_hsa_circ_377308,RMVar_hsa_circ_330140,RMVar_hsa_circ_18140,RMVar_hsa_circ_72628,RMVar_hsa_circ_11125,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_335361,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_334772,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228576,RMVar_hsa_circ_228577,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574 75108 RMVar_ID_75108 Human_SNP_ID_202972440 m1A Human chr4 - 128091092 128091092 128091092 CGTCCTCTTCCCCGTCCTCGGCCTCTTCCTCGACCTCTAAAGGAACCTCGGATATTACCACCCTC CGTCCTCTTCCCCGTCCTCGGCCTCTTCCTCGGCCTCTAAAGGAACCTCGGATATTACCACCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:128091041..128091175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 75109 RMVar_ID_75109 Human_SNP_ID_203020170 m1A Human chr4 - 128287474 128287474 128287474 GCCTCGCATGAAGAAGCGGGACTTCAGCTTGGAGCAGCTGCGCCAGTACGACGGCTCCCGCAACC GCCTCGCATGAAGAAGCGGGACTTCAGCTTGGGGCAGCTGCGCCAGTACGACGGCTCCCGCAACC T C PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:128287351..128287500 32194978 MeRIP-seq:(Medium) rs149247614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_613268,Human_RBP_ID_1634972,Human_RBP_ID_5121264,Human_RBP_ID_5150866,Human_RBP_ID_7267208,Human_RBP_ID_9335073,Human_RBP_ID_9354509,Human_RBP_ID_15044553,Human_RBP_ID_22510227,Human_RBP_ID_27062393 75110 RMVar_ID_75110 Human_SNP_ID_203020243 m1A Human chr4 + 128287568 128287568 128287568 CCCGGCCCCGGCCCCCAGACCCCGCCGCCCCCAGCGCACCCACAGCCGGTAGGCCCCCAGCAGCA CCCGGCCCCGGCCCCCAGACCCCGCCGCCCCCCGCGCACCCACAGCCGGTAGGCCCCCAGCAGCA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:128287468..128287572 26863410 MeRIP-seq:(Medium) rs1369826614 Functional Loss SNV dbSNP153 33..33 33 - - - 75111 RMVar_ID_75111 Human_SNP_ID_203020322 m1A Human chr4 - 128287718 128287718 128287718 GGAGTGGCAGCGAGAGCAGCAACGACGGCGGCAGCGAGAGTCCAGGCGACGCGGGAGCGGCAGCG GGAGTGGCAGCGAGAGCAGCAACGACGGCGGCTGCGAGAGTCCAGGCGACGCGGGAGCGGCAGCG T A PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:128287504..128287800 26863196 MeRIP-seq:(Medium) rs1418668221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249547,Human_RBP_ID_3966396,Human_RBP_ID_4794707,Human_RBP_ID_5326046,Human_RBP_ID_9435842,Human_RBP_ID_15044554,Human_RBP_ID_22457990,Human_RBP_ID_24547726,Human_RBP_ID_26349555 75112 RMVar_ID_75112 Human_SNP_ID_203020330 m1A Human chr4 - 128287726 128287726 128287726 CACCCTGGGGAGTGGCAGCGAGAGCAGCAACGACGGCGGCAGCGAGAGTCCAGGCGACGCGGGAG CACCCTGGGGAGTGGCAGCGAGAGCAGCAACGGCGGCGGCAGCGAGAGTCCAGGCGACGCGGGAG T C PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:128287697..128287781 26863410 MeRIP-seq:(Medium) rs746067498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249547,Human_RBP_ID_3749556,Human_RBP_ID_3966396,Human_RBP_ID_4772849,Human_RBP_ID_5326046,Human_RBP_ID_8943765,Human_RBP_ID_9435842,Human_RBP_ID_15044554,Human_RBP_ID_17662136,Human_RBP_ID_18424911,Human_RBP_ID_22457990,Human_RBP_ID_24547726,Human_RBP_ID_26349555 75113 RMVar_ID_75113 Human_SNP_ID_203020336 m1A Human chr4 - 128287742 128287742 128287742 GGGACGTGAAGCTAGGCACCCTGGGGAGTGGCAGCGAGAGCAGCAACGACGGCGGCAGCGAGAGT GGGACGTGAAGCTAGGCACCCTGGGGAGTGGCGGCGAGAGCAGCAACGACGGCGGCAGCGAGAGT T C PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:128287489..128287815 26863196 MeRIP-seq:(Medium) rs1486275542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249547,Human_RBP_ID_3749556,Human_RBP_ID_3966396,Human_RBP_ID_4794707,Human_RBP_ID_5326046,Human_RBP_ID_8943765,Human_RBP_ID_9435842,Human_RBP_ID_15044554,Human_RBP_ID_17662136,Human_RBP_ID_18424911,Human_RBP_ID_22457990,Human_RBP_ID_22611818,Human_RBP_ID_24547726,Human_RBP_ID_26349555,Human_RBP_ID_27841866 75114 RMVar_ID_75114 Human_SNP_ID_203020345 m1A Human chr4 - 128287757 128287757 128287757 TGGCGGCTGGTGATGGGGACGTGAAGCTAGGCACCCTGGGGAGTGGCAGCGAGAGCAGCAACGAC TGGCGGCTGGTGATGGGGACGTGAAGCTAGGCGCCCTGGGGAGTGGCAGCGAGAGCAGCAACGAC T C PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:128287328..128288144;chr4:128287227..128288133;chr4:128287186..128288332 26863196 MeRIP-seq:(Medium) rs982889961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72889,Human_RBP_ID_249547,Human_RBP_ID_3749556,Human_RBP_ID_4794707,Human_RBP_ID_5326046,Human_RBP_ID_5507358,Human_RBP_ID_8583969,Human_RBP_ID_8943765,Human_RBP_ID_9435842,Human_RBP_ID_15044554,Human_RBP_ID_17662136,Human_RBP_ID_18424911,Human_RBP_ID_22287830,Human_RBP_ID_22457990,Human_RBP_ID_22611818,Human_RBP_ID_24547726,Human_RBP_ID_26349555,Human_RBP_ID_27841866 75115 RMVar_ID_75115 Human_SNP_ID_203020350 m1A Human chr4 - 128287766 128287766 128287766 GGGCAGTGATGGCGGCTGGTGATGGGGACGTGAAGCTAGGCACCCTGGGGAGTGGCAGCGAGAGC GGGCAGTGATGGCGGCTGGTGATGGGGACGTGCAGCTAGGCACCCTGGGGAGTGGCAGCGAGAGC T G PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:128287476..128287825 26863196 MeRIP-seq:(Medium) rs944978445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72889,Human_RBP_ID_249547,Human_RBP_ID_3749556,Human_RBP_ID_4794707,Human_RBP_ID_5326046,Human_RBP_ID_5507358,Human_RBP_ID_8583969,Human_RBP_ID_8943765,Human_RBP_ID_9435842,Human_RBP_ID_15044554,Human_RBP_ID_17662136,Human_RBP_ID_18424911,Human_RBP_ID_22457990,Human_RBP_ID_22611818,Human_RBP_ID_24547726,Human_RBP_ID_26349555,Human_RBP_ID_27841866 75116 RMVar_ID_75116 Human_SNP_ID_203020351 m1A Human chr4 + 128287768 128287768 128287768 TCTCGCTGCCACTCCCCAGGGTGCCTAGCTTCACGTCCCCATCACCAGCCGCCATCACTGCCCGC TCTCGCTGCCACTCCCCAGGGTGCCTAGCTTCCCGTCCCCATCACCAGCCGCCATCACTGCCCGC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:128287426..128287825 26863196 MeRIP-seq:(Medium) rs1353098455 Functional Loss SNV dbSNP153 33..33 33 - - - 75117 RMVar_ID_75117 Human_SNP_ID_203062389 m1A Human chr4 + 128474810 128474810 128474810 GCGGGGAGCGGGATCGTCTTAGACCATGAGGGAGGATGAGGTGCTGAGAGCTGGAAGAATGAAGA GCGGGGAGCGGGATCGTCTTAGACCATGAGGGGGGATGAGGTGCTGAGAGCTGGAAGAATGAAGA A G LINC02615 Ensembl:ENSG00000251432 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:128474752..128474954 26863196 MeRIP-seq:(Medium) rs1256653467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_606608 RMVar_hsa_circ_359762,RMVar_hsa_circ_47470 75118 RMVar_ID_75118 Human_SNP_ID_203062399 m1A Human chr4 + 128474878 128474878 128474878 AAGTGGCCTGATGAGGAGGTGGAGGTGTGAGAAGTGACAAAGAGTCTGTGAGGAGAATGAGGAAG AAGTGGCCTGATGAGGAGGTGGAGGTGTGAGAGGTGACAAAGAGTCTGTGAGGAGAATGAGGAAG A G LINC02615 Ensembl:ENSG00000251432 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:128474723..128474988 26863196 MeRIP-seq:(Medium) rs889962175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607862 RMVar_hsa_circ_359762,RMVar_hsa_circ_47470 75119 RMVar_ID_75119 Human_SNP_ID_203143185 m1A Human chr4 + 128810281 128810281 128810281 GAGGATGATTTTTGGATCCTGAGAATTGATCTATGTTGGATCAGTAAGTTTTATTATGATTTTTT GAGGATGATTTTTGGATCCTGAGAATTGATCTGTGTTGGATCAGTAAGTTTTATTATGATTTTTT A G JADE1 Ensembl:ENSG00000077684 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:128810109..128810316 26863196 MeRIP-seq:(Medium) rs565963190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_606721 75120 RMVar_ID_75120 Human_SNP_ID_203151002 m1A Human chr4 - 128841717 128841717 128841717 TGCTCACCCATGTCCACAGTCTTACCCAGCACACCCAGAGGAACCTGCCAGACCTACATTCCCAG TGCTCACCCATGTCCACAGTCTTACCCAGCACTCCCAGAGGAACCTGCCAGACCTACATTCCCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:128841713..128842006 26863196 MeRIP-seq:(Medium) rs1186896566 Functional Loss SNV dbSNP153 33..33 33 - - - 75121 RMVar_ID_75121 Human_SNP_ID_203151022 m1A Human chr4 + 128841779 128841779 128841779 GCACCCCCGGGGAGAATATTTGGAGCAAGAAAAGAGCAAAGAGTTCAGGAGAAACCCATGTTGAT GCACCCCCGGGGAGAATATTTGGAGCAAGAAAGGAGCAAAGAGTTCAGGAGAAACCCATGTTGAT A G JADE1 Ensembl:ENSG00000077684 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:128841777..128841879 26863196 MeRIP-seq:(Medium) rs1301679852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5940,RMVar_hsa_circ_228600,RMVar_hsa_circ_277472,RMVar_hsa_circ_288583,RMVar_hsa_circ_322391,RMVar_hsa_circ_326867,RMVar_hsa_circ_335688,RMVar_hsa_circ_302944,RMVar_hsa_circ_285972,RMVar_hsa_circ_66164,RMVar_hsa_circ_228601,RMVar_hsa_circ_228598,RMVar_hsa_circ_228599,RMVar_hsa_circ_228597 75122 RMVar_ID_75122 Human_SNP_ID_203154992 m1A Human chr4 - 128859104 128859104 128859104 GCTCCACTCTTTCCTCCTCCTTCCCCAATCCAACTCGGGCCAGAGGCGTTTGTCATGTATTCACA GCTCCACTCTTTCCTCCTCCTTCCCCAATCCAGCTCGGGCCAGAGGCGTTTGTCATGTATTCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:128859095..128859200 26863196 MeRIP-seq:(Medium) rs191261143 Functional Loss SNV dbSNP153 33..33 33 - - - 75123 RMVar_ID_75123 Human_SNP_ID_203156054 m1A Human chr4 + 128862884 128862884 128862884 AGAAGATACTCCTGGCAGTGAGGTGCTAAGTCATCACTGAGGCTGTGTGTGTGTGTGTGTGTGCG AGAAGATACTCCTGGCAGTGAGGTGCTAAGTCTTCACTGAGGCTGTGTGTGTGTGTGTGTGTGCG A T JADE1 Ensembl:ENSG00000077684 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:128862833..128862944 26863196 MeRIP-seq:(Medium) rs1423750572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15045351,Human_RBP_ID_24035207 RMVar_hsa_circ_322391,RMVar_hsa_circ_228597 75124 RMVar_ID_75124 Human_SNP_ID_203870420 m1A Human chr4 + 131725130 131725130 131725130 CCGGGGGATGGGTCCCTGAGACTTGGCGAAGTAGGAGCCCTGTGTGATTGTGCGTCAGAGTCGGG CCGGGGGATGGGTCCCTGAGACTTGGCGAAGTGGGAGCCCTGTGTGATTGTGCGTCAGAGTCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:131725086..131725154;chr4:131725083..131725174 26863196 MeRIP-seq:(Medium) rs111556283 Functional Loss SNV dbSNP153 33..33 33 - - - 75125 RMVar_ID_75125 Human_SNP_ID_204268275 m1A Human chr4 + 133262924 133262924 133262924 TGTCCTATTGGTTTGAACCATAAAGTTAGCTCATGCTGGTACCAAGCACCAACAGGATATTTGTC TGTCCTATTGGTTTGAACCATAAAGTTAGCTCCTGCTGGTACCAAGCACCAACAGGATATTTGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:133262873..133263002 26863196 MeRIP-seq:(Medium) rs1304196880 Functional Loss SNV dbSNP153 33..33 33 - - - 75126 RMVar_ID_75126 Human_SNP_ID_204269445 m1A Human chr4 + 133267078 133267078 133267078 GTTGAACAGTCCGATTTTCAGTGGGGTCCCATACAGATGGGACGCGGCTTAGGAGGAATCCCGGG GTTGAACAGTCCGATTTTCAGTGGGGTCCCATTCAGATGGGACGCGGCTTAGGAGGAATCCCGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:133267058..133267209 26863196 MeRIP-seq:(Medium) rs539274708 Functional Loss SNV dbSNP153 33..33 33 - - - 75127 RMVar_ID_75127 Human_SNP_ID_204502508 m1A Human chr4 - 134201754 134201754 134201754 TGGCAGCGAGTGCGCGGGAAGTTCAGCGCGCGAGTTCCGGGCTTCCCGCCCGCCCGCAGACGACC TGGCAGCGAGTGCGCGGGAAGTTCAGCGCGCGGGTTCCGGGCTTCCCGCCCGCCCGCAGACGACC T C PABPC4L,AC015631.1 Ensembl:ENSG00000254535,Ensembl:ENSG00000251199 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:134201641..134201753 26863196 MeRIP-seq:(Medium) rs1255741409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_608233 75128 RMVar_ID_75128 Human_SNP_ID_490455157 m1A Human chr12 - 10221883 10221883 10221883 CGCACACACACCCCTCCCCTACCCCCAAGTCCAGGTGCTCCCATCTGCTGGGCTTCCAACCACTC CGCACACACACCCCTCCCCTACCCCCAAGTCCTGGTGCTCCCATCTGCTGGGCTTCCAACCACTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10221834..10222036 26863196 MeRIP-seq:(Medium) rs764072840 Functional Loss SNV dbSNP153 33..33 33 - - - 75129 RMVar_ID_75129 Human_SNP_ID_490455163 m1A Human chr12 + 10221896 10221896 10221896 CCCAGCAGATGGGAGCACCTGGACTTGGGGGTAGGGGAGGGGTGTGTGTGCGCGACATGGGGAAA CCCAGCAGATGGGAGCACCTGGACTTGGGGGTCGGGGAGGGGTGTGTGTGCGCGACATGGGGAAA A C GABARAPL1 Ensembl:ENSG00000139112 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:10221848..10222007 26863196 MeRIP-seq:(Medium) rs767674400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754779,Human_RBP_ID_27417815 75130 RMVar_ID_75130 Human_SNP_ID_490455213 m1A Human chr12 - 10222156 10222156 10222156 TCTCTGGCCCCAACTTGTCCACCTCCTGACCCATCTATGAAACTGCACAACAATTAAACCCCAGG TCTCTGGCCCCAACTTGTCCACCTCCTGACCCTTCTATGAAACTGCACAACAATTAAACCCCAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:10222106..10222288 26863196 MeRIP-seq:(Medium) rs956713051 Functional Loss SNV dbSNP153 33..33 33 - - - 75131 RMVar_ID_75131 Human_SNP_ID_490555192 m1A Human chr12 - 10613533 10613533 10613533 GCTGCGTTTTCGGCGGGCTTCCCGGGTACAAAAATGGCTGTGGCTAGCGATTTCTACCTGCGCTA GCTGCGTTTTCGGCGGGCTTCCCGGGTACAAATATGGCTGTGGCTAGCGATTTCTACCTGCGCTA T A MAGOHB Ensembl:ENSG00000111196 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10613344..10613600 26863196 MeRIP-seq:(Medium) rs774959011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115569,Human_RBP_ID_989428,Human_RBP_ID_4249258,Human_RBP_ID_9322439,Human_RBP_ID_11793868,Human_RBP_ID_22169137,Human_RBP_ID_22492153,Human_RBP_ID_27154596 Human_Splice_Rec_1339363,Human_Splice_Rec_1339381,Human_Splice_Rec_1339391,Human_Splice_Rec_1339407,Human_Splice_Rec_1339417,Human_Splice_Rec_1339425,Human_Splice_Rec_1339433,Human_Splice_Rec_1339437 Human_miRNA_ID_1342286 75132 RMVar_ID_75132 Human_SNP_ID_490555203 m1A Human chr12 + 10613547 10613547 10613547 ATCGCTAGCCACAGCCATTTTTGTACCCGGGAAGCCCGCCGAAAACGCAGCCAACGTGTCCCCCG ATCGCTAGCCACAGCCATTTTTGTACCCGGGATGCCCGCCGAAAACGCAGCCAACGTGTCCCCCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:10613250..10613600 26863196 MeRIP-seq:(Medium) rs766500121 Functional Loss SNV dbSNP153 33..33 33 - - - 75133 RMVar_ID_75133 Human_SNP_ID_490575784 m1A Human chr12 + 10699599 10699599 10699599 TTATTGCTTGGATGTTTCTTTGGTGTTGGTTAAGGTTGTGGCCTGCTTTTTGCTTTATTTCTGAA TTATTGCTTGGATGTTTCTTTGGTGTTGGTTACGGTTGTGGCCTGCTTTTTGCTTTATTTCTGAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10699450..10699688 26863196 MeRIP-seq:(Medium) rs1334010840 Functional Loss SNV dbSNP153 33..33 33 - - - 75134 RMVar_ID_75134 Human_SNP_ID_490576212 m1A Human chr12 + 10701330 10701330 10701330 CTGCTCTGCTGGGTGGGTGGAGCAGGGTTCTCAGTTGGTGCTTCACCTGCCTTGGCCTAAAATGC CTGCTCTGCTGGGTGGGTGGAGCAGGGTTCTCGGTTGGTGCTTCACCTGCCTTGGCCTAAAATGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10701204..10701404 26863196 MeRIP-seq:(Medium) rs752371088 Functional Loss SNV dbSNP153 33..33 33 - - - 75135 RMVar_ID_75135 Human_SNP_ID_490576218 m1A Human chr12 - 10701350 10701350 10701350 CTGATTTATGGCTTTGTTTTGCATTTTAGGCCAAGGCAGGTGAAGCACCAACTGAGAACCCTGCT CTGATTTATGGCTTTGTTTTGCATTTTAGGCCGAGGCAGGTGAAGCACCAACTGAGAACCCTGCT T C YBX3 Ensembl:ENSG00000060138 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:10701301..10701375 26863196 MeRIP-seq:(Medium) rs1452549950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755392,Human_RBP_ID_810060,Human_RBP_ID_3942752,Human_RBP_ID_18188722,Human_RBP_ID_26806522 Human_Splice_Rec_1339502,Human_Splice_Rec_1339503,Human_Splice_Rec_1339520,Human_Splice_Rec_1339521,Human_Splice_Rec_1339534,Human_Splice_Rec_1339535,Human_Splice_Rec_1339540,Human_Splice_Rec_1339541,Human_Splice_Rec_1339548,Human_Splice_Rec_1339549,Human_Splice_Rec_1339554,Human_Splice_Rec_1339555,Human_Splice_Rec_1339560,Human_Splice_Rec_1339561,Human_Splice_Rec_1339570,Human_Splice_Rec_1339572,Human_Splice_Rec_1339582,Human_Splice_Rec_1339590 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420 75136 RMVar_ID_75136 Human_SNP_ID_490576449 m1A Human chr12 - 10702048 10702048 10702048 AGAAAATCAGCAAGCCACCAGTGGTCCAAACCAGCCGTCTGTTCGCCGTGGATACCGGCGTCCCT AGAAAATCAGCAAGCCACCAGTGGTCCAAACCGGCCGTCTGTTCGCCGTGGATACCGGCGTCCCT T C YBX3 Ensembl:ENSG00000060138 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:10701951..10702075 32194978 MeRIP-seq:(Medium) rs1025590123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115235,Human_RBP_ID_229655,Human_RBP_ID_1463444,Human_RBP_ID_4249322,Human_RBP_ID_8364172,Human_RBP_ID_11794892,Human_RBP_ID_18976857,Human_RBP_ID_22792840,Human_RBP_ID_26900329 Human_Splice_Rec_1339500,Human_Splice_Rec_1339501,Human_Splice_Rec_1339518,Human_Splice_Rec_1339519,Human_Splice_Rec_1339533,Human_Splice_Rec_1339538,Human_Splice_Rec_1339539,Human_Splice_Rec_1339546,Human_Splice_Rec_1339547,Human_Splice_Rec_1339552,Human_Splice_Rec_1339553,Human_Splice_Rec_1339558,Human_Splice_Rec_1339559,Human_Splice_Rec_1339568,Human_Splice_Rec_1339569,Human_Splice_Rec_1339571,Human_Splice_Rec_1339580,Human_Splice_Rec_1339581,Human_Splice_Rec_1339588,Human_Splice_Rec_1339589,Human_Splice_Rec_1339596 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420 75137 RMVar_ID_75137 Human_SNP_ID_490576490 m1A Human chr12 - 10702136 10702136 10702136 GCACCTGTTCTATTTTCTTCTGTGTTCCCTACAGCAGGGGACCTCCTCGCCCACGACCTGCCCCA GCACCTGTTCTATTTTCTTCTGTGTTCCCTACTGCAGGGGACCTCCTCGCCCACGACCTGCCCCA T A YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:10702101..10702150 26863196 MeRIP-seq:(Medium) rs112456748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115235,Human_RBP_ID_755393,Human_RBP_ID_9366148,Human_RBP_ID_25016736 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420 75138 RMVar_ID_75138 Human_SNP_ID_490576491 m1A Human chr12 - 10702136 10702136 10702136 GCACCTGTTCTATTTTCTTCTGTGTTCCCTACAGCAGGGGACCTCCTCGCCCACGACCTGCCCCA GCACCTGTTCTATTTTCTTCTGTGTTCCCTACCGCAGGGGACCTCCTCGCCCACGACCTGCCCCA T G YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:10702101..10702150 26863196 MeRIP-seq:(Medium) rs112456748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115235,Human_RBP_ID_755393,Human_RBP_ID_9366148,Human_RBP_ID_25016736 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420 75139 RMVar_ID_75139 Human_SNP_ID_490578502 m1A Human chr12 - 10709876 10709876 10709876 GGTAAAATTGCAACTGAGACTTCTCTTCAGCAATCCTCACCCTTCCGTCCTTCTCTGCCTCCTCT GGTAAAATTGCAACTGAGACTTCTCTTCAGCAGTCCTCACCCTTCCGTCCTTCTCTGCCTCCTCT T C YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10709874..10710038 26863196 MeRIP-seq:(Medium) rs750133676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2301283 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420,RMVar_hsa_circ_154863,RMVar_hsa_circ_319054 75140 RMVar_ID_75140 Human_SNP_ID_490578558 m1A Human chr12 + 10709979 10709979 10709979 GTCAAAGGTCTGTCCCACGTGGTAAGGCGGGAACCGCCGCTGCCGGTACTGAGGGCGATACTGGG GTCAAAGGTCTGTCCCACGTGGTAAGGCGGGACCCGCCGCTGCCGGTACTGAGGGCGATACTGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:10709965..10710050 26863196 MeRIP-seq:(Medium) rs771079117 Functional Loss SNV dbSNP153 33..33 33 - - - 75141 RMVar_ID_75141 Human_SNP_ID_490578636 m1A Human chr12 - 10710095 10710095 10710095 TTTGCTTCGCTAGTACGCTGGGGAGGAGGAGGAGGAAGGGAGCGGCAGCAGTGAAGGATTTGACC TTTGCTTCGCTAGTACGCTGGGGAGGAGGAGGCGGAAGGGAGCGGCAGCAGTGAAGGATTTGACC T G YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr12:10710045..10710146 26863410 MeRIP-seq:(Medium) rs756291706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228410,Human_RBP_ID_752817,Human_RBP_ID_809494,Human_RBP_ID_872172,Human_RBP_ID_6245075,Human_RBP_ID_18160456,Human_RBP_ID_18975386,Human_RBP_ID_22644632,Human_RBP_ID_22792842,Human_RBP_ID_23535006,Human_RBP_ID_24557717,Human_RBP_ID_25016740,Human_RBP_ID_26321217,Human_RBP_ID_26900339 Human_Splice_Rec_1339514,Human_Splice_Rec_1339592,Human_Splice_Rec_1339604 RMVar_hsa_circ_1060,RMVar_hsa_circ_63420,RMVar_hsa_circ_154863,RMVar_hsa_circ_319054 75142 RMVar_ID_75142 Human_SNP_ID_490579412 m1A Human chr12 - 10713282 10713282 10713282 TGACTGGCCCGGATGGAGTTCCTGTGGAAGGGAGTCGTTACGCTGCAGATCGGCGCCGTTACAGA TGACTGGCCCGGATGGAGTTCCTGTGGAAGGGGGTCGTTACGCTGCAGATCGGCGCCGTTACAGA T C YBX3 Ensembl:ENSG00000060138 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:10713173..10713377 26863196 MeRIP-seq:(Medium) rs1388862217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228412,Human_RBP_ID_409516,Human_RBP_ID_809443,Human_RBP_ID_872173,Human_RBP_ID_989451,Human_RBP_ID_1463463,Human_RBP_ID_1785891,Human_RBP_ID_3391704,Human_RBP_ID_4198804,Human_RBP_ID_6126807,Human_RBP_ID_8364202,Human_RBP_ID_8775558,Human_RBP_ID_9276915,Human_RBP_ID_9364657,Human_RBP_ID_11795212,Human_RBP_ID_17650052,Human_RBP_ID_17683255,Human_RBP_ID_17808279,Human_RBP_ID_18433450,Human_RBP_ID_18616654,Human_RBP_ID_18976865,Human_RBP_ID_22492166,Human_RBP_ID_23535027,Human_RBP_ID_26321219,Human_RBP_ID_27806459 Human_Splice_Rec_1339496,Human_Splice_Rec_1339497,Human_Splice_Rec_1339512,Human_Splice_Rec_1339513,Human_Splice_Rec_1339530,Human_Splice_Rec_1339564,Human_Splice_Rec_1339565,Human_Splice_Rec_1339576,Human_Splice_Rec_1339577,Human_Splice_Rec_1339602,Human_Splice_Rec_1339603,Human_Splice_Rec_1339610,Human_Splice_Rec_1339611,Human_Splice_Rec_1339622 RMVar_hsa_circ_63420,RMVar_hsa_circ_49273,RMVar_hsa_circ_154863,RMVar_hsa_circ_319054,RMVar_hsa_circ_299135,RMVar_hsa_circ_339477,RMVar_hsa_circ_154864 75143 RMVar_ID_75143 Human_SNP_ID_490582088 m1A Human chr12 + 10723209 10723209 10723209 GTGGTCGCGGCGGCCGGGGCTCGCTCTCGGGGAGGCCGGGGCGGATCTCGCGGCGCAGGCGGCGG GTGGTCGCGGCGGCCGGGGCTCGCTCTCGGGGCGGCCGGGGCGGATCTCGCGGCGCAGGCGGCGG A C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr12:10723112..10723312 26863410 MeRIP-seq:(Medium) rs975950289 Functional Loss SNV dbSNP153 33..33 33 - - - 75144 RMVar_ID_75144 Human_SNP_ID_490582089 m1A Human chr12 + 10723209 10723209 10723209 GTGGTCGCGGCGGCCGGGGCTCGCTCTCGGGGAGGCCGGGGCGGATCTCGCGGCGCAGGCGGCGG GTGGTCGCGGCGGCCGGGGCTCGCTCTCGGGGGGGCCGGGGCGGATCTCGCGGCGCAGGCGGCGG A G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr12:10723112..10723312 26863410 MeRIP-seq:(Medium) rs975950289 Functional Loss SNV dbSNP153 33..33 33 - - - 75145 RMVar_ID_75145 Human_SNP_ID_490582098 m1A Human chr12 + 10723233 10723233 10723233 TCTCGGGGAGGCCGGGGCGGATCTCGCGGCGCAGGCGGCGGCGGCCGAGGTGGGGTCGCGCGGCG TCTCGGGGAGGCCGGGGCGGATCTCGCGGCGCGGGCGGCGGCGGCCGAGGTGGGGTCGCGCGGCG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:10722905..10723350 26863410 MeRIP-seq:(Medium) rs1201762292 Functional Loss SNV dbSNP153 33..33 33 - - - 75146 RMVar_ID_75146 Human_SNP_ID_490582127 m1A Human chr12 - 10723274 10723274 10723274 AGCCCAAGAGAGAGCGCGCAGCACGAAGCTCGAGCCGCCTCCGCCGCGCGACCCCACCTCGGCCG AGCCCAAGAGAGAGCGCGCAGCACGAAGCTCGGGCCGCCTCCGCCGCGCGACCCCACCTCGGCCG T C YBX3 Ensembl:ENSG00000060138 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:10722844..10723400;chr12:10722921..10723350;chr12:10722851..10723350 26863196 MeRIP-seq:(Medium) rs1476048486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229660,Human_RBP_ID_4246526,Human_RBP_ID_6126874,Human_RBP_ID_22532415 75147 RMVar_ID_75147 Human_SNP_ID_490702706 m1A Human chr12 - 11171692 11171692 11171692 CCCTGAGGAGCTCCGCTAGCAGCTAAGAGGGCAGCCACGAAGAGCGCCTGAGCACTCTCGCGAGA CCCTGAGGAGCTCCGCTAGCAGCTAAGAGGGCCGCCACGAAGAGCGCCTGAGCACTCTCGCGAGA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:11171521..11171750 26863410 MeRIP-seq:(Medium) rs1176070769 Functional Loss SNV dbSNP153 33..33 33 - - - 75148 RMVar_ID_75148 Human_SNP_ID_490838303 m1A Human chr12 + 11649890 11649890 11649890 CCCGGGTCCCCGCGCCGCGCCGCGACCTGCAGACCCCGCCGCCGCGCTCGGGCCCGTCTCCCACG CCCGGGTCCCCGCGCCGCGCCGCGACCTGCAGCCCCCGCCGCCGCGCTCGGGCCCGTCTCCCACG A C ETV6 Ensembl:ENSG00000139083 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:11649841..11649922 26863196 MeRIP-seq:(Medium) rs555463308 Functional Loss SNV dbSNP153 33..33 33 - - - 75149 RMVar_ID_75149 Human_SNP_ID_490838304 m1A Human chr12 + 11649890 11649890 11649890 CCCGGGTCCCCGCGCCGCGCCGCGACCTGCAGACCCCGCCGCCGCGCTCGGGCCCGTCTCCCACG CCCGGGTCCCCGCGCCGCGCCGCGACCTGCAGGCCCCGCCGCCGCGCTCGGGCCCGTCTCCCACG A G ETV6 Ensembl:ENSG00000139083 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:11649841..11649922 26863196 MeRIP-seq:(Medium) rs555463308 Functional Loss SNV dbSNP153 33..33 33 - - - 75150 RMVar_ID_75150 Human_SNP_ID_490838323 m1A Human chr12 + 11649944 11649944 11649944 CGTCTCCCACGCCCCCGCCGCCCCGCGCGCCCAACTCCGCCGGCCGCCCCGCCCCGCCCCGCGCG CGTCTCCCACGCCCCCGCCGCCCCGCGCGCCCGACTCCGCCGGCCGCCCCGCCCCGCCCCGCGCG A G ETV6 Ensembl:ENSG00000139083 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:11649846..11650047 26863410 MeRIP-seq:(Medium) rs968066319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4250429,Human_RBP_ID_24365261 75151 RMVar_ID_75151 Human_SNP_ID_490838342 m1A Human chr12 + 11649983 11649980 11649983 CCGGCCGCCCCGCCCCGCCCCGCGCGCTCCAGACCCCCGGGGCGGCTGCCGGGAGAGATGCTGGA CCGGCCGCCCCGCCCCGCCCCGCGCGCTCC___CCCCCGGGGCGGCTGCCGGGAGAGATGCTGGA CAGA C ETV6 Ensembl:ENSG00000139083 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:11649888..11650014 26863196 MeRIP-seq:(Medium) rs1286939288 Functional Loss DEL dbSNP153 31..33 33 - - - 75152 RMVar_ID_75152 Human_SNP_ID_490859915 m1A Human chr12 - 11735348 11735348 11735348 CCACCCACTGATCTCACCACTAATCTCACCAAAGACCAACTCCCATAACCGTAACTCGCAGAGAC CCACCCACTGATCTCACCACTAATCTCACCAACGACCAACTCCCATAACCGTAACTCGCAGAGAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:11735246..11735375 26863196 MeRIP-seq:(Medium) rs924273483 Functional Loss SNV dbSNP153 33..33 33 - - - 75153 RMVar_ID_75153 Human_SNP_ID_490957702 m1A Human chr12 - 12111065 12111049 12111065 GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGGAGGCGCGCGGCGGAGGCGGCTGCGGCGAGCAAG GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGG________________CGGCTGCGGCGAGCAAG GCCTCCGCCGCGCGCCT G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:12111024..12111128 26863410 MeRIP-seq:(Medium) rs570715828 Functional Loss DEL dbSNP153 33..48 33 - - - 75154 RMVar_ID_75154 Human_SNP_ID_490957713 m1A Human chr12 - 12111065 12111065 12111065 GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGGAGGCGCGCGGCGGAGGCGGCTGCGGCGAGCAAG GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGGCGGCGCGCGGCGGAGGCGGCTGCGGCGAGCAAG T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:12111024..12111128 26863410 MeRIP-seq:(Medium) rs1482680824 Functional Loss SNV dbSNP153 33..33 33 - - - 75155 RMVar_ID_75155 Human_SNP_ID_490957736 m1A Human chr12 + 12111101 12111100 12111102 CCGCCGCCGCGGACTCCGGCAGCTTTATCGCCAGAGTCCCTGAACTCTCGCTTTCTTTTTTATCC CCGCCGCCGCGGACTCCGGCAGCTTTATCGCC__AGTCCCTGAACTCTCGCTTTCTTTTTTATCC CAG C BCL2L14 Ensembl:ENSG00000121380 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:12111001..12111125 26863410 MeRIP-seq:(Medium) rs1565505967 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_2784168 RMVar_hsa_circ_101358,RMVar_hsa_circ_154897 75156 RMVar_ID_75156 Human_SNP_ID_490957745 m1A Human chr12 - 12111126 12111123 12111126 GGGCACGCCGGTGACGCGATGCAGGGGATAAAAAAGAAAGCGAGAGTTCAGGGACTCTGGCGATA GGGCACGCCGGTGACGCGATGCAGGGGATAAA___GAAAGCGAGAGTTCAGGGACTCTGGCGATA CTTT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr12:12111026..12111128;chr12:12111025..12111131 26863410 MeRIP-seq:(Medium) rs568226358 Functional Loss DEL dbSNP153 33..35 33 - - - 75157 RMVar_ID_75157 Human_SNP_ID_490957746 m1A Human chr12 - 12111126 12111123 12111126 GGGCACGCCGGTGACGCGATGCAGGGGATAAAAAAGAAAGCGAGAGTTCAGGGACTCTGGCGATA GGGCACGCCGGTGACGCGATGCAGGGGATAAA_AAGAAAGCGAGAGTTCAGGGACTCTGGCGATA CTTT CTT - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr12:12111026..12111128;chr12:12111025..12111131 26863410 MeRIP-seq:(Medium) rs568226358 Functional Loss DEL dbSNP153 33..33 33 - - - 75158 RMVar_ID_75158 Human_SNP_ID_490999143 m1A Human chr12 - 12266951 12266951 12266951 CGCCGGGGGAGGAGGCGGCGGGATGGAAGCAGACGCTGGCGTCGCGCGAGCCCGGGGCCGAGCGG CGCCGGGGGAGGAGGCGGCGGGATGGAAGCAGGCGCTGGCGTCGCGCGAGCCCGGGGCCGAGCGG T C LRP6 Ensembl:ENSG00000070018 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:12266736..12266994;chr12:12266658..12267002;chr12:12266696..12267012 26863196 MeRIP-seq:(Medium) rs535719082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229679,Human_RBP_ID_755437,Human_RBP_ID_4246011,Human_RBP_ID_8229600,Human_RBP_ID_9322442,Human_RBP_ID_9366172,Human_RBP_ID_18417403,Human_RBP_ID_18976871,Human_RBP_ID_22436350 75159 RMVar_ID_75159 Human_SNP_ID_491022936 m1A Human chr12 + 12350386 12350386 12350386 TCCGGGCTCCCGGCCCCAGCGCTGAGCCCCGCAGGGAGGTGGCTCCCCCCACCGCCCCGCGCTCC TCCGGGCTCCCGGCCCCAGCGCTGAGCCCCGCTGGGAGGTGGCTCCCCCCACCGCCCCGCGCTCC A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:12350337..12350485 26863196 MeRIP-seq:(Medium) rs1289670315 Functional Loss SNV dbSNP153 33..33 33 - - - 75160 RMVar_ID_75160 Human_SNP_ID_491024712 m1A Human chr12 + 12357118 12357118 12357118 CCCGGAAGGAGCGAGCTTGCGGAGCGTGAACCAGTGAGTGAAAGCGGCGCCGCCCGCCGGCCGCA CCCGGAAGGAGCGAGCTTGCGGAGCGTGAACCCGTGAGTGAAAGCGGCGCCGCCCGCCGGCCGCA A C BORCS5 Ensembl:ENSG00000165714 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:12357096..12357258 26863196 MeRIP-seq:(Medium) rs767816521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1340313 75161 RMVar_ID_75161 Human_SNP_ID_491058462 m1A Human chr12 + 12477451 12477451 12477451 AGCTTCTTGGGGATGCTGGCTTCCTCCTTATCAGGACTGGTTTCGGGAGTCTGCTCCGATAGTTC AGCTTCTTGGGGATGCTGGCTTCCTCCTTATCGGGACTGGTTTCGGGAGTCTGCTCCGATAGTTC A G L13712-001,NONHSAG010521.2 RNACentral:URS0000334622,RNACentral:URS00009BB46F misc_RNA,lincRNA intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:12477401..12477500 32194978 MeRIP-seq:(Medium) rs1366238865 Functional Loss SNV dbSNP153 33..33 33 - - - 75162 RMVar_ID_75162 Human_SNP_ID_491078948 m1A Human chr12 - 12561777 12561777 12561777 CCGCTGCGCGGCGCTTGGACCGGGCCCCGCCGAGAGGAGCGGCCGCCGCGGGACGCGGCACCTTT CCGCTGCGCGGCGCTTGGACCGGGCCCCGCCGGGAGGAGCGGCCGCCGCGGGACGCGGCACCTTT T C DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12561773..12561868 26863196 MeRIP-seq:(Medium) rs1285429535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874314,Human_RBP_ID_5171649,Human_RBP_ID_5348178,Human_RBP_ID_9415829,Human_RBP_ID_17650618,Human_RBP_ID_19825793,Human_RBP_ID_22040534,Human_RBP_ID_22710317,Human_RBP_ID_22736895,Human_RBP_ID_24365276 RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 75163 RMVar_ID_75163 Human_SNP_ID_491079090 m1A Human chr12 + 12562209 12562209 12562209 CCCTCGGGCCCCCCTCGCCTCCCGGACTTGCGAGGCGCCGCCGCGGAGCCGAGAGGGCGGCTGCG CCCTCGGGCCCCCCTCGCCTCCCGGACTTGCGCGGCGCCGCCGCGGAGCCGAGAGGGCGGCTGCG A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:12562171..12562270 26863196 MeRIP-seq:(Medium) rs907382947 Functional Loss SNV dbSNP153 33..33 33 - - - 75164 RMVar_ID_75164 Human_SNP_ID_491079303 m1A Human chr12 + 12562729 12562729 12562729 AGCCCCGGGGAAAGGAGGAGACAGGCGAGGGCAGGGCGGTGGGCGCCGGGCGGGGCCGCGCGCTC AGCCCCGGGGAAAGGAGGAGACAGGCGAGGGCGGGGCGGTGGGCGCCGGGCGGGGCCGCGCGCTC A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:12562706..12562821;chr12:12562702..12562808 26863196 MeRIP-seq:(Medium) rs996964871 Functional Loss SNV dbSNP153 33..33 33 - - - 75165 RMVar_ID_75165 Human_SNP_ID_491098460 m1A Human chr12 + 12635824 12635824 12635824 GTAAAGAAGCCCGGTAAACGTGGTCGGAAGCCAGCCAAAATTGACTTGAAAGCAAAACTTGAGAG GTAAAGAAGCCCGGTAAACGTGGTCGGAAGCCGGCCAAAATTGACTTGAAAGCAAAACTTGAGAG A G CREBL2 Ensembl:ENSG00000111269 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:12635732..12635850;chr12:12635739..12635853 26863196 MeRIP-seq:(Medium) rs778791306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414715 Human_Splice_Rec_1340366,Human_Splice_Rec_1340370 Human_miRNA_ID_195648,Human_miRNA_ID_696322,Human_miRNA_ID_701259,Human_miRNA_ID_1461123 RMVar_hsa_circ_154950,RMVar_hsa_circ_290666,RMVar_hsa_circ_319982,RMVar_hsa_circ_154951 75166 RMVar_ID_75166 Human_SNP_ID_491117530 m1A Human chr12 - 12717429 12717429 12717429 GGGGACAGGGGAGGGGGAGAAAAACACCCCGAAAAGACGAGCCCCCTTTTTTTAGTGGCCCAATA GGGGACAGGGGAGGGGGAGAAAAACACCCCGAGAAGACGAGCCCCCTTTTTTTAGTGGCCCAATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12717314..12717591 26863196 MeRIP-seq:(Medium) rs544835565 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_345 75167 RMVar_ID_75167 Human_SNP_ID_491117672 m1A Human chr12 + 12717809 12717809 12717809 GTTTTGTTCGGTTTTGTTTTTTTGAGAGTGCGAGAGAGGCGGTCGTGCAGACCCGGGAGAAAGAT GTTTTGTTCGGTTTTGTTTTTTTGAGAGTGCGCGAGAGGCGGTCGTGCAGACCCGGGAGAAAGAT A C CDKN1B Ensembl:ENSG00000111276 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:12717511..12717808 32194978 MeRIP-seq:(Medium) rs972365866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33919,Human_RBP_ID_811172,Human_RBP_ID_877894,Human_RBP_ID_3397784,Human_RBP_ID_4211439,Human_RBP_ID_5491185,Human_RBP_ID_6151374,Human_RBP_ID_11873839,Human_RBP_ID_21884979,Human_RBP_ID_22039171,Human_RBP_ID_23546792 RMVar_hsa_circ_154952,RMVar_hsa_circ_104420 75168 RMVar_ID_75168 Human_SNP_ID_491117673 m1A Human chr12 + 12717809 12717809 12717809 GTTTTGTTCGGTTTTGTTTTTTTGAGAGTGCGAGAGAGGCGGTCGTGCAGACCCGGGAGAAAGAT GTTTTGTTCGGTTTTGTTTTTTTGAGAGTGCGGGAGAGGCGGTCGTGCAGACCCGGGAGAAAGAT A G CDKN1B Ensembl:ENSG00000111276 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:12717511..12717808 32194978 MeRIP-seq:(Medium) rs972365866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33919,Human_RBP_ID_811172,Human_RBP_ID_877894,Human_RBP_ID_3397784,Human_RBP_ID_4211439,Human_RBP_ID_5491185,Human_RBP_ID_6151374,Human_RBP_ID_11873839,Human_RBP_ID_21884979,Human_RBP_ID_22039171,Human_RBP_ID_23546792 RMVar_hsa_circ_154952,RMVar_hsa_circ_104420 75169 RMVar_ID_75169 Human_SNP_ID_491117694 m1A Human chr12 + 12717854 12717839 12717854 TGCAGACCCGGGAGAAAGATGTCAAACGTGCGAGTGTCTAACGGGAGCCCTAGCCTGGAGCGGAT TGCAGACCCGGGAGAAAG_______________GTGTCTAACGGGAGCCCTAGCCTGGAGCGGAT GATGTCAAACGTGCGA G CDKN1B Ensembl:ENSG00000111276 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:12717363..12718231;chr12:12717651..12718055;chr12:12717626..12717933 26863196 MeRIP-seq:(Medium) rs758613901 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_1467578,Human_RBP_ID_4246536,Human_RBP_ID_6151381,Human_RBP_ID_23546792 RMVar_hsa_circ_154952,RMVar_hsa_circ_104420 75170 RMVar_ID_75170 Human_SNP_ID_491120435 m1A Human chr12 + 12725961 12725961 12725961 GGCGGGGGTGCGCGGGGCGGTCAGCGATCTGCAGCTTCGCGGGGACAGAGATGTAACCCAACTCG GGCGGGGGTGCGCGGGGCGGTCAGCGATCTGCCGCTTCGCGGGGACAGAGATGTAACCCAACTCG A C APOLD1 Ensembl:ENSG00000178878 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12725845..12726212 26863196 MeRIP-seq:(Medium) rs757006225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18433845,Human_RBP_ID_18621641 75171 RMVar_ID_75171 Human_SNP_ID_491142712 m1A Human chr12 + 12813402 12813402 12813402 GGCGGCACCCGAGGAACACGATTCTCCGACCGAAGCGTCCCAGCCGATTGTGGAAGAGGAGGAAA GGCGGCACCCGAGGAACACGATTCTCCGACCGCAGCGTCCCAGCCGATTGTGGAAGAGGAGGAAA A C DDX47,APOLD1 Ensembl:ENSG00000213782,Ensembl:ENSG00000178878 Protein coding,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:12813351..12813500 26863196 MeRIP-seq:(Medium) rs983186320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37087,Human_RBP_ID_230169,Human_RBP_ID_414828,Human_RBP_ID_1467657,Human_RBP_ID_1790456,Human_RBP_ID_4252478,Human_RBP_ID_8369407,Human_RBP_ID_9364672,Human_RBP_ID_18621683,Human_RBP_ID_22793555,Human_RBP_ID_23547069,Human_RBP_ID_26321226 Human_Splice_Rec_1340425,Human_Splice_Rec_1340433,Human_Splice_Rec_1340461,Human_Splice_Rec_1340477,Human_Splice_Rec_1340505,Human_Splice_Rec_1340509,Human_Splice_Rec_1340531,Human_Splice_Rec_1340551,Human_Splice_Rec_1340553,Human_Splice_Rec_1340569 75172 RMVar_ID_75172 Human_SNP_ID_491142916 m1A Human chr12 - 12814157 12814157 12814157 TTGGTGGGTTTTGTCCATCCCAACTGGTCACAAGCTTCACACAACACATCTGTCACACCCTTGGA TTGGTGGGTTTTGTCCATCCCAACTGGTCACATGCTTCACACAACACATCTGTCACACCCTTGGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12813351..12814225 26863196 MeRIP-seq:(Medium) rs751716292 Functional Loss SNV dbSNP153 33..33 33 - - - 75173 RMVar_ID_75173 Human_SNP_ID_491142917 m1A Human chr12 - 12814157 12814157 12814157 TTGGTGGGTTTTGTCCATCCCAACTGGTCACAAGCTTCACACAACACATCTGTCACACCCTTGGA TTGGTGGGTTTTGTCCATCCCAACTGGTCACACGCTTCACACAACACATCTGTCACACCCTTGGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12813351..12814225 26863196 MeRIP-seq:(Medium) rs751716292 Functional Loss SNV dbSNP153 33..33 33 - - - 75174 RMVar_ID_75174 Human_SNP_ID_491144479 m1A Human chr12 - 12821274 12821274 12821274 ACAAACGCTGCGGGGTCTCCAGCAGTGCGTTTAGAATGGGCAAAGCAAAGGCGCCTGTCTTTCCA ACAAACGCTGCGGGGTCTCCAGCAGTGCGTTTCGAATGGGCAAAGCAAAGGCGCCTGTCTTTCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12821167..12821273 26863196 MeRIP-seq:(Medium) rs898503925 Functional Loss SNV dbSNP153 33..33 33 - - - 75175 RMVar_ID_75175 Human_SNP_ID_491144950 m1A Human chr12 + 12822724 12822724 12822724 ATCGGAAAACATTCCTCTTCTCTGCCACCATGACCAAGAAGGTGAAATTTGCTAGGACTTTTGTT ATCGGAAAACATTCCTCTTCTCTGCCACCATGGCCAAGAAGGTGAAATTTGCTAGGACTTTTGTT A G DDX47,APOLD1 Ensembl:ENSG00000213782,Ensembl:ENSG00000178878 Protein coding,Protein coding exon,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:12822674..12823309 32194978 MeRIP-seq:(Medium) rs1452867582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35709,Human_RBP_ID_874320,Human_RBP_ID_8778588,Human_RBP_ID_9366175,Human_RBP_ID_18257293 Human_Splice_Rec_1340442,Human_Splice_Rec_1340443,Human_Splice_Rec_1340470,Human_Splice_Rec_1340471,Human_Splice_Rec_1340486,Human_Splice_Rec_1340487,Human_Splice_Rec_1340518,Human_Splice_Rec_1340519,Human_Splice_Rec_1340540,Human_Splice_Rec_1340541,Human_Splice_Rec_1340560,Human_Splice_Rec_1340561,Human_Splice_Rec_1340576,Human_Splice_Rec_1340577,Human_Splice_Rec_1340588,Human_Splice_Rec_1340589 RMVar_hsa_circ_68078,RMVar_hsa_circ_79162,RMVar_hsa_circ_266949,RMVar_hsa_circ_154955 75176 RMVar_ID_75176 Human_SNP_ID_491146865 m1A Human chr12 + 12829478 12829478 12829478 GAAGAAACGCTCGCGAGAGGATGCTGGAGATAATGATGACACAGAGGGTGCTATTGGTGTCAGGA GAAGAAACGCTCGCGAGAGGATGCTGGAGATACTGATGACACAGAGGGTGCTATTGGTGTCAGGA A C DDX47,APOLD1 Ensembl:ENSG00000213782,Ensembl:ENSG00000178878 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:12829421..12829550 26863196 MeRIP-seq:(Medium) rs749342404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37100,Human_RBP_ID_414838,Human_RBP_ID_8369418,Human_RBP_ID_8778604,Human_RBP_ID_9366177,Human_RBP_ID_11874748,Human_RBP_ID_22039839,Human_RBP_ID_23547116,Human_RBP_ID_26321228,Human_RBP_ID_27805295 Human_Splice_Rec_1340454,Human_Splice_Rec_1340496,Human_Splice_Rec_1340530,Human_Splice_Rec_1340550,Human_Splice_Rec_1340568 75177 RMVar_ID_75177 Human_SNP_ID_491146866 m1A Human chr12 + 12829478 12829478 12829478 GAAGAAACGCTCGCGAGAGGATGCTGGAGATAATGATGACACAGAGGGTGCTATTGGTGTCAGGA GAAGAAACGCTCGCGAGAGGATGCTGGAGATAGTGATGACACAGAGGGTGCTATTGGTGTCAGGA A G DDX47,APOLD1 Ensembl:ENSG00000213782,Ensembl:ENSG00000178878 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:12829421..12829550 26863196 MeRIP-seq:(Medium) rs749342404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37100,Human_RBP_ID_414838,Human_RBP_ID_8369418,Human_RBP_ID_8778604,Human_RBP_ID_9366177,Human_RBP_ID_11874748,Human_RBP_ID_22039839,Human_RBP_ID_23547116,Human_RBP_ID_26321228,Human_RBP_ID_27805295 Human_Splice_Rec_1340454,Human_Splice_Rec_1340496,Human_Splice_Rec_1340530,Human_Splice_Rec_1340550,Human_Splice_Rec_1340568 75178 RMVar_ID_75178 Human_SNP_ID_491152702 m1A Human chr12 + 12851202 12851202 12851202 GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCACCTGCTACTGAGTAAGGGGCATTCCTGTTACA GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCCCCTGCTACTGAGTAAGGGGCATTCCTGTTACA A C AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs3825274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9013270 75179 RMVar_ID_75179 Human_SNP_ID_491152703 m1A Human chr12 + 12851202 12851202 12851202 GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCACCTGCTACTGAGTAAGGGGCATTCCTGTTACA GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCGCCTGCTACTGAGTAAGGGGCATTCCTGTTACA A G AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs3825274 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_9013270 75180 RMVar_ID_75180 Human_SNP_ID_491152704 m1A Human chr12 + 12851202 12851202 12851202 GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCACCTGCTACTGAGTAAGGGGCATTCCTGTTACA GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCTCCTGCTACTGAGTAAGGGGCATTCCTGTTACA A T AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs3825274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9013270 75181 RMVar_ID_75181 Human_SNP_ID_491158177 m1A Human chr12 + 12870830 12870828 12870831 GGAGGAGATGTTTACAGGGGAACTCTCGGACGAGGAGGAGGAGTTAGCCAAGTGAAGAATGGGGG GGAGGAGATGTTTACAGGGGAACTCTCGGAC___GAGGAGGAGTTAGCCAAGTGAAGAATGGGGG CGAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:12870794..12870935 26863196 MeRIP-seq:(Medium) rs1242515405 Functional Loss DEL dbSNP153 32..34 33 - - - 75182 RMVar_ID_75182 Human_SNP_ID_491164128 m1A Human chr12 + 12893136 12893136 12893136 ACCTTGAGTCAGGAAGACTGATTTCTCCTCCCAGCTCCGCAGGAACATGGAACTGTGATCAGGCA ACCTTGAGTCAGGAAGACTGATTTCTCCTCCCGGCTCCGCAGGAACATGGAACTGTGATCAGGCA A G GPRC5A Ensembl:ENSG00000013588 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:12893135..12893296 32194978 MeRIP-seq:(Medium) rs1043479371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118946,RMVar_hsa_circ_154958,RMVar_hsa_circ_76214,RMVar_hsa_circ_154957 75183 RMVar_ID_75183 Human_SNP_ID_491168384 m1A Human chr12 - 12908742 12908742 12908742 TTCATTGCGACGAGGAGCGGAAAGCTCAGAAAAGACATTGACGTTGGTCCTATTCATGGTCAGGA TTCATTGCGACGAGGAGCGGAAAGCTCAGAAACGACATTGACGTTGGTCCTATTCATGGTCAGGA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:12908701..12908775 26863196 MeRIP-seq:(Medium) rs780766101 Functional Loss SNV dbSNP153 33..33 33 - - - 75184 RMVar_ID_75184 Human_SNP_ID_491169523 m1A Human chr12 + 12912652 12912652 12912652 TCTTCTGAGAAAACTGTACAAGACACTACGGGAACAGTTTGCCTCCCTCCCAGCCTCAACCACAA TCTTCTGAGAAAACTGTACAAGACACTACGGGGACAGTTTGCCTCCCTCCCAGCCTCAACCACAA A G GPRC5A Ensembl:ENSG00000013588 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:12912601..12912675 32194978 MeRIP-seq:(Medium) rs903441305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3397958,Human_RBP_ID_19702018 Human_miRNA_ID_1314704,Human_miRNA_ID_2029637,Human_miRNA_ID_2475714,Human_miRNA_ID_2690123,Human_miRNA_ID_2693385,Human_miRNA_ID_2961499 RMVar_hsa_circ_86566,RMVar_hsa_circ_118946,RMVar_hsa_circ_154958,RMVar_hsa_circ_117550,RMVar_hsa_circ_154960,RMVar_hsa_circ_154961 75185 RMVar_ID_75185 Human_SNP_ID_491181002 m1A Human chr12 + 12950062 12950049 12950063 GAACCAGCTTCACTAGATTGGAGGCATGAGCTAAGAGGCATGAGAAACAGAGAGCAAAGAGAACC GAACCAGCTTCACTAGATTG______________GAGGCATGAGAAACAGAGAGCAAAGAGAACC GGAGGCATGAGCTAA G GPRC5D-AS1 Ensembl:ENSG00000247498 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:12950036..12950167 26863196 MeRIP-seq:(Medium) rs1474001517 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_5560058 75186 RMVar_ID_75186 Human_SNP_ID_491181019 m1A Human chr12 + 12950092 12950092 12950092 CTAAGAGGCATGAGAAACAGAGAGCAAAGAGAACCCCAAAGAGAAAGTAGCGTACGGGGGCAGTT CTAAGAGGCATGAGAAACAGAGAGCAAAGAGACCCCCAAAGAGAAAGTAGCGTACGGGGGCAGTT A C GPRC5D-AS1 Ensembl:ENSG00000247498 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:12950064..12950169 26863196 MeRIP-seq:(Medium) rs781435483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5560058 75187 RMVar_ID_75187 Human_SNP_ID_491190495 m1A Human chr12 - 12989402 12989402 12989402 GTACCTTCTCTCTCTCTAGGAAGAAGTTGCCTATGAAGAAAGGGCCTGTGAAGGCGGCAAATTTG GTACCTTCTCTCTCTCTAGGAAGAAGTTGCCTCTGAAGAAAGGGCCTGTGAAGGCGGCAAATTTG T G HEBP1 Ensembl:ENSG00000013583 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:12989351..12989468 26863196 MeRIP-seq:(Medium) rs756678921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4252631 Human_Splice_Rec_1340666,Human_Splice_Rec_1340672,Human_Splice_Rec_1340686 RMVar_hsa_circ_337992 75188 RMVar_ID_75188 Human_SNP_ID_491192812 m1A Human chr12 - 13000072 13000072 13000072 TGATCAAGAACTCGCTGTTCGGAAGCGTAGAGACGTGGCCTTGGCAGGTCCTAAGCAAAGGGGAC TGATCAAGAACTCGCTGTTCGGAAGCGTAGAGGCGTGGCCTTGGCAGGTCCTAAGCAAAGGGGAC T C HEBP1 Ensembl:ENSG00000013583 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:13000026..13000230 26863196 MeRIP-seq:(Medium) rs745462736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415056 Human_Splice_Rec_1340665,Human_Splice_Rec_1340671,Human_Splice_Rec_1340685 75189 RMVar_ID_75189 Human_SNP_ID_491192854 m1A Human chr12 + 13000223 13000192 13000224 CCGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CC________________________________GGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAG C GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:13000122..13000300 26863410 MeRIP-seq:(Medium) rs878915334 Functional Loss DEL dbSNP153 3..34 33 - - - 75190 RMVar_ID_75190 Human_SNP_ID_491192855 m1A Human chr12 + 13000223 13000192 13000224 CCGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CCGGCGGCAG________________________GGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAG CGGCGGCAG GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:13000122..13000300 26863410 MeRIP-seq:(Medium) rs878915334 Functional Loss DEL dbSNP153 11..34 33 - - - 75191 RMVar_ID_75191 Human_SNP_ID_491192856 m1A Human chr12 + 13000223 13000192 13000224 CCGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CCGGCGGCAGGGCGGCAG________________GGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAG CGGCGGCAGGGCGGCAG GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:13000122..13000300 26863410 MeRIP-seq:(Medium) rs878915334 Functional Loss DEL dbSNP153 19..34 33 - - - 75192 RMVar_ID_75192 Human_SNP_ID_491192857 m1A Human chr12 + 13000223 13000192 13000224 CCGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CCGGCGGCAGGGCGGCAGGGCGGCAG________GGCGGCAGGGTGGCAGGGCGGCAAGGCGGCG CGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAG CGGCGGCAGGGCGGCAGGGCGGCAG GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:13000122..13000300 26863410 MeRIP-seq:(Medium) rs878915334 Functional Loss DEL dbSNP153 27..34 33 - - - 75193 RMVar_ID_75193 Human_SNP_ID_491192869 m1A Human chr12 + 13000207 13000207 13000207 CCACGGGCAGCGACCACCGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCA CCACGGGCAGCGACCACCGGCGGCAGGGCGGCCGGGCGGCAGGGCGGCAGGGCGGCAGGGTGGCA A C GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:12999946..13000283 26863196 MeRIP-seq:(Medium) rs1565496007 Functional Loss SNV dbSNP153 33..33 33 - - - 75194 RMVar_ID_75194 Human_SNP_ID_491192890 m1A Human chr12 + 13000247 13000224 13000248 AGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGA AGGGCGGCAG________________________GGCGGCGGGACGGCGAGGCGGCGAGGCGAGA GGGCGGCAGGGTGGCAGGGCGGCAA G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:13000151..13000275 26863410 MeRIP-seq:(Medium) rs1187482260 Functional Loss DEL dbSNP153 11..34 33 - - - 75195 RMVar_ID_75195 Human_SNP_ID_491192890 m1A Human chr12 + 13000248 13000224 13000248 GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGCGGCAG________________________GGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGCGGCAGGGTGGCAGGGCGGCAA G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:13000149..13000275 26863410 MeRIP-seq:(Medium) rs1187482260 Functional Loss DEL dbSNP153 10..33 33 - - - 75196 RMVar_ID_75196 Human_SNP_ID_491192905 m1A Human chr12 + 13000247 13000232 13000248 AGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGA AGGGCGGCAGGGCGGCAG________________GGCGGCGGGACGGCGAGGCGGCGAGGCGAGA GGGTGGCAGGGCGGCAA G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:13000151..13000275 26863410 MeRIP-seq:(Medium) rs1565496061 Functional Loss DEL dbSNP153 19..34 33 - - - 75197 RMVar_ID_75197 Human_SNP_ID_491192905 m1A Human chr12 + 13000248 13000232 13000248 GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGCGGCAGGGCGGCAG________________GGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGTGGCAGGGCGGCAA G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:13000149..13000275 26863410 MeRIP-seq:(Medium) rs1565496061 Functional Loss DEL dbSNP153 18..33 33 - - - 75198 RMVar_ID_75198 Human_SNP_ID_491192931 m1A Human chr12 + 13000247 13000247 13000247 AGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGA AGGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCGAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGA A G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:13000151..13000275 26863410 MeRIP-seq:(Medium) rs1274203234 Functional Loss SNV dbSNP153 33..33 33 - - - 75199 RMVar_ID_75199 Human_SNP_ID_491192933 m1A Human chr12 + 13000248 13000248 13000248 GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAGGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG A G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:13000149..13000275 26863410 MeRIP-seq:(Medium) rs1036063783 Functional Loss SNV dbSNP153 33..33 33 - - - 75200 RMVar_ID_75200 Human_SNP_ID_491203051 m1A Human chr12 + 13044572 13044572 13044572 CCAGACTCAGCTGCAGGCGCCCGGTGCCGAGGAGGGTGCAGTCCCTTGGGGCTGGGGTCTCTGTG CCAGACTCAGCTGCAGGCGCCCGGTGCCGAGGTGGGTGCAGTCCCTTGGGGCTGGGGTCTCTGTG A T FAM234B Ensembl:ENSG00000084444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:13044452..13044675 26863196 MeRIP-seq:(Medium) rs1184223544 Functional Loss SNV dbSNP153 33..33 33 - - - 75201 RMVar_ID_75201 Human_SNP_ID_491238938 m1A Human chr12 + 13196844 13196843 13196845 CGGACCAGGGCTGCTGCCAGCACCTGCCACTCAGAGCGCCTCTGTCGCTGGGACCCTTCAGGTAG CGGACCAGGGCTGCTGCCAGCACCTGCCACTC__AGCGCCTCTGTCGCTGGGACCCTTCAGGTAG CAG C EMP1 Ensembl:ENSG00000134531 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:13196743..13196907 26863196 MeRIP-seq:(Medium) rs960216073 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1340873,Human_Splice_Rec_1340877,Human_Splice_Rec_1340879,Human_Splice_Rec_1340883,Human_Splice_Rec_1340887,Human_Splice_Rec_1340895,Human_Splice_Rec_1340901,Human_Splice_Rec_1340903,Human_Splice_Rec_1340905 75202 RMVar_ID_75202 Human_SNP_ID_491243241 m1A Human chr12 + 13215048 13215047 13215048 CTTCTGGGTCATGCACTGAGGTCCACAGACCTACTGCACTGAGTTAAAATAGCGGTACAAGTTCT CTTCTGGGTCATGCACTGAGGTCCACAGACCT_CTGCACTGAGTTAAAATAGCGGTACAAGTTCT TA T EMP1 Ensembl:ENSG00000134531 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:13214998..13215082 32194978 MeRIP-seq:(Medium) rs937779216 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1340886 Human_miRNA_ID_501095,Human_miRNA_ID_508315,Human_miRNA_ID_830628 75203 RMVar_ID_75203 Human_SNP_ID_491243405 m1A Human chr12 + 13215745 13215745 13215745 TGGTAGCTCTGGCTTAGACACCACCTGGAGTGATCACCTCTTGGGGACCCTGCCTATCCCACTTC TGGTAGCTCTGGCTTAGACACCACCTGGAGTGGTCACCTCTTGGGGACCCTGCCTATCCCACTTC A G EMP1 Ensembl:ENSG00000134531 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:13215694..13215792 32194978 MeRIP-seq:(Medium) rs1019965896 Functional Loss SNV dbSNP153 33..33 33 - - - 75204 RMVar_ID_75204 Human_SNP_ID_491530856 m1A Human chr12 + 14365723 14365723 14365723 GAGGCGGCGGCGGTGGCAGCGGCGGCGCGGCGACTGAAGCGCGCGAAAAGCTGAGGCGGCAACGT GAGGCGGCGGCGGTGGCAGCGGCGGCGCGGCGGCTGAAGCGCGCGAAAAGCTGAGGCGGCAACGT A G ATF7IP Ensembl:ENSG00000171681 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:14365696..14365829 26863196 MeRIP-seq:(Medium) rs906404810 Functional Loss SNV dbSNP153 33..33 33 - - - 75205 RMVar_ID_75205 Human_SNP_ID_491558340 m1A Human chr12 + 14478451 14478451 14478451 CTGGGGTGCCAACAAGTGGACCATCTCAGACCACCATACACTTACTACCTACAGGTAAATTTGTT CTGGGGTGCCAACAAGTGGACCATCTCAGACCGCCATACACTTACTACCTACAGGTAAATTTGTT A G ATF7IP Ensembl:ENSG00000171681 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:14478401..14478533 26863196 MeRIP-seq:(Medium) rs934545657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_991078,Human_RBP_ID_3399713,Human_RBP_ID_8066938,Human_RBP_ID_8779479,Human_RBP_ID_9255085,Human_RBP_ID_9277603,Human_RBP_ID_17237364,Human_RBP_ID_17353259,Human_RBP_ID_17469844,Human_RBP_ID_17814505,Human_RBP_ID_18526580,Human_RBP_ID_22420936,Human_RBP_ID_22756227,Human_RBP_ID_27625958 Human_Splice_Rec_1341033,Human_Splice_Rec_1341107,Human_Splice_Rec_1341131,Human_Splice_Rec_1341167,Human_Splice_Rec_1341231,Human_Splice_Rec_1341239 Human_miRNA_ID_2168450,Human_miRNA_ID_2169974 RMVar_hsa_circ_5750,RMVar_hsa_circ_60089,RMVar_hsa_circ_94869,RMVar_hsa_circ_50948,RMVar_hsa_circ_375829,RMVar_hsa_circ_155002,RMVar_hsa_circ_155001,RMVar_hsa_circ_7606,RMVar_hsa_circ_155009,RMVar_hsa_circ_330190,RMVar_hsa_circ_70589,RMVar_hsa_circ_112080,RMVar_hsa_circ_155010,RMVar_hsa_circ_155011 75206 RMVar_ID_75206 Human_SNP_ID_491627653 m1A Human chr12 - 14771002 14771002 14771002 GCGCCACCGGAAGGTGCTGCGGGACAATATCCAAGGCATTACAAAGCCGGCGATTCGCCGTCTCG GCGCCACCGGAAGGTGCTGCGGGACAATATCCCAGGCATTACAAAGCCGGCGATTCGCCGTCTCG T G H4-16 Ensembl:ENSG00000197837 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:14770951..14771125 26863196 MeRIP-seq:(Medium) rs1342539682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415862,Human_RBP_ID_991118,Human_RBP_ID_1468946,Human_RBP_ID_9014112,Human_RBP_ID_17814601,Human_RBP_ID_18160463 75207 RMVar_ID_75207 Human_SNP_ID_491628618 m1A Human chr12 - 14774434 14774434 14774434 ACCTCTCGCCTACAACTCCAGAGACGGAGACAAACCGCTCTCGGCGTCCGGTACCGGAATGCAAC ACCTCTCGCCTACAACTCCAGAGACGGAGACACACCGCTCTCGGCGTCCGGTACCGGAATGCAAC T G lnc-HIST4H4-2 RNACentral:URS0000D574C5 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:14774351..14774860 26863196 MeRIP-seq:(Medium) rs937270048 Functional Loss SNV dbSNP153 33..33 33 - - - 75208 RMVar_ID_75208 Human_SNP_ID_491628624 m1A Human chr12 - 14774447 14774447 14774447 ACCGGACATGATCACCTCTCGCCTACAACTCCAGAGACGGAGACAAACCGCTCTCGGCGTCCGGT ACCGGACATGATCACCTCTCGCCTACAACTCCCGAGACGGAGACAAACCGCTCTCGGCGTCCGGT T G lnc-HIST4H4-2 RNACentral:URS0000D574C5 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:14774401..14774450;chr12:14774401..14774632 26863196 MeRIP-seq:(Medium) rs944584731 Functional Loss SNV dbSNP153 33..33 33 - - - 75209 RMVar_ID_75209 Human_SNP_ID_491628664 m1A Human chr12 + 14774544 14774544 14774544 GGCCAAATCCCGCTCCTCCCGCGCGGGCCTGCAGTTCCCGGTGGGCCGAGTGCACAGACTGCTGC GGCCAAATCCCGCTCCTCCCGCGCGGGCCTGCGGTTCCCGGTGGGCCGAGTGCACAGACTGCTGC A G H2AJ Ensembl:ENSG00000246705 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:14774426..14774975 32194978 MeRIP-seq:(Medium) rs1428326420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247319 75210 RMVar_ID_75210 Human_SNP_ID_491632169 m1A Human chr12 + 14789129 14789129 14789129 CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGAGCTCCTGAAAAGAGAAAAATGATAAATTAATG CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGCGCTCCTGAAAAGAGAAAAATGATAAATTAATG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:14789032..14789166 26863410 MeRIP-seq:(Medium) rs752115693 Functional Loss SNV dbSNP153 33..33 33 - - - 75211 RMVar_ID_75211 Human_SNP_ID_491632170 m1A Human chr12 + 14789129 14789129 14789129 CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGAGCTCCTGAAAAGAGAAAAATGATAAATTAATG CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGGGCTCCTGAAAAGAGAAAAATGATAAATTAATG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:14789032..14789166 26863410 MeRIP-seq:(Medium) rs752115693 Functional Loss SNV dbSNP153 33..33 33 - - - 75212 RMVar_ID_75212 Human_SNP_ID_491635058 m1A Human chr12 - 14801266 14801265 14801266 ATGATGAAGTAGGAGAGTGTTAAAAATTGCAAATATTAGGGAATTTCTTTCTCTGTGGCTTAATT ATGATGAAGTAGGAGAGTGTTAAAAATTGCAA_TATTAGGGAATTTCTTTCTCTGTGGCTTAATT AT A WBP11 Ensembl:ENSG00000084463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:14801263..14801341 26863196 MeRIP-seq:(Medium) rs1411445130 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_34077,RMVar_hsa_circ_53797 75213 RMVar_ID_75213 Human_SNP_ID_491635101 m1A Human chr12 + 14801427 14801427 14801427 GTATGGTTTACTTGTTCATTAAAAAAAGAAAAACCTGTGAAGGTGAAGACAAAGAAATAGCTTAT GTATGGTTTACTTGTTCATTAAAAAAAGAAAAGCCTGTGAAGGTGAAGACAAAGAAATAGCTTAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:14801378..14801464 26863196 MeRIP-seq:(Medium) rs778664253 Functional Loss SNV dbSNP153 33..33 33 - - - 75214 RMVar_ID_75214 Human_SNP_ID_491871173 m1A Human chr12 + 15789383 15789383 15789383 GGGCGAGACCGCCTCGCTAGCTGCTGCCTGTGAAGTCTGGAGCCGCCCGCCCGCTCGCAGCCAGT GGGCGAGACCGCCTCGCTAGCTGCTGCCTGTGGAGTCTGGAGCCGCCCGCCCGCTCGCAGCCAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:15789300..15789388 26863196 MeRIP-seq:(Medium) rs891055996 Functional Loss SNV dbSNP153 33..33 33 - - - 75215 RMVar_ID_75215 Human_SNP_ID_491893078 m1A Human chr12 + 15882500 15882500 15882500 TTCCTCCCTCCCTCCCTTTCCCTCCCTCGTCGACTGTTGCTTGCTGGTCGCAGACTCCCTGACCC TTCCTCCCTCCCTCCCTTTCCCTCCCTCGTCGCCTGTTGCTTGCTGGTCGCAGACTCCCTGACCC A C STRAP Ensembl:ENSG00000023734 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:15882399..15882550;chr12:15882401..15882750 26863410 MeRIP-seq:(Medium) rs1413523462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32979,Human_RBP_ID_415953,Human_RBP_ID_4253276,Human_RBP_ID_5126824,Human_RBP_ID_5314514,Human_RBP_ID_11891713,Human_RBP_ID_17075045,Human_RBP_ID_17561364,Human_RBP_ID_18934328,Human_RBP_ID_23550666,Human_RBP_ID_26904897 Human_miRNA_ID_2026344,Human_miRNA_ID_2215987 RMVar_hsa_circ_82332,RMVar_hsa_circ_155087 75216 RMVar_ID_75216 Human_SNP_ID_491893079 m1A Human chr12 + 15882500 15882500 15882500 TTCCTCCCTCCCTCCCTTTCCCTCCCTCGTCGACTGTTGCTTGCTGGTCGCAGACTCCCTGACCC TTCCTCCCTCCCTCCCTTTCCCTCCCTCGTCGGCTGTTGCTTGCTGGTCGCAGACTCCCTGACCC A G STRAP Ensembl:ENSG00000023734 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:15882399..15882550;chr12:15882401..15882750 26863410 MeRIP-seq:(Medium) rs1413523462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32979,Human_RBP_ID_415953,Human_RBP_ID_4253276,Human_RBP_ID_5126824,Human_RBP_ID_5314514,Human_RBP_ID_11891713,Human_RBP_ID_17075045,Human_RBP_ID_17561364,Human_RBP_ID_18934328,Human_RBP_ID_23550666,Human_RBP_ID_26904897 Human_miRNA_ID_2026344,Human_miRNA_ID_2215987 RMVar_hsa_circ_82332,RMVar_hsa_circ_155087 75217 RMVar_ID_75217 Human_SNP_ID_491893088 m1A Human chr12 - 15882538 15882528 15882539 CAATCCGGTGGCACCGAGGTTAGGGAGGGGTGAGGGAGGGGTCAGGGAGTCTGCGACCAGCAAGC CAATCCGGTGGCACCGAGGTTAGGGAGGGGT___________CAGGGAGTCTGCGACCAGCAAGC GACCCCTCCCTC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:15882488..15882635 26863196 MeRIP-seq:(Medium) rs981250339 Functional Loss DEL dbSNP153 32..42 33 - - - 75218 RMVar_ID_75218 Human_SNP_ID_491893100 m1A Human chr12 - 15882575 15882572 15882575 GACACTAGGGCTGGGCTGGGCAACAGGAAAAGAAGGGCAATCCGGTGGCACCGAGGTTAGGGAGG GACACTAGGGCTGGGCTGGGCAACAGGAAAAG___GGCAATCCGGTGGCACCGAGGTTAGGGAGG CCTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:15882401..15882725 26863196 MeRIP-seq:(Medium) rs1288183851 Functional Loss DEL dbSNP153 33..35 33 - - - 75219 RMVar_ID_75219 Human_SNP_ID_491893156 m1A Human chr12 - 15882692 15882692 15882692 GTCTGTCTCATTGCCATGGCGGCGGCGAAGCCAGCGACCGGACTGGCGAGCTGAGGGTCGTCGTT GTCTGTCTCATTGCCATGGCGGCGGCGAAGCCGGCGACCGGACTGGCGAGCTGAGGGTCGTCGTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:15882676..15882700 26863196 MeRIP-seq:(Medium) rs369260760 Functional Loss SNV dbSNP153 33..33 33 - - - 75220 RMVar_ID_75220 Human_SNP_ID_491893157 m1A Human chr12 - 15882692 15882692 15882692 GTCTGTCTCATTGCCATGGCGGCGGCGAAGCCAGCGACCGGACTGGCGAGCTGAGGGTCGTCGTT GTCTGTCTCATTGCCATGGCGGCGGCGAAGCCCGCGACCGGACTGGCGAGCTGAGGGTCGTCGTT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:15882676..15882700 26863196 MeRIP-seq:(Medium) rs369260760 Functional Loss SNV dbSNP153 33..33 33 - - - 75221 RMVar_ID_75221 Human_SNP_ID_491911893 m1A Human chr12 + 15956996 15956996 15956996 GAATCACCCGGCAGTTCTGAGGCGTGCGGAACAAATCCAGGCTCGCAGAACCGTGAAAAAGGAGT GAATCACCCGGCAGTTCTGAGGCGTGCGGAACTAATCCAGGCTCGCAGAACCGTGAAAAAGGAGT A T DERA Ensembl:ENSG00000023697 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:15956896..15957050 26863196 MeRIP-seq:(Medium) rs368479950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874326,Human_RBP_ID_4247331 Human_Splice_Rec_1343066,Human_Splice_Rec_1343067,Human_Splice_Rec_1343080,Human_Splice_Rec_1343081,Human_Splice_Rec_1343090,Human_Splice_Rec_1343091,Human_Splice_Rec_1343108,Human_Splice_Rec_1343109,Human_Splice_Rec_1343120,Human_Splice_Rec_1343121,Human_Splice_Rec_1343132,Human_Splice_Rec_1343133,Human_Splice_Rec_1343146,Human_Splice_Rec_1343147,Human_Splice_Rec_1343158,Human_Splice_Rec_1343159 RMVar_hsa_circ_106717,RMVar_hsa_circ_35249,RMVar_hsa_circ_20004,RMVar_hsa_circ_282436,RMVar_hsa_circ_292981,RMVar_hsa_circ_118870,RMVar_hsa_circ_155090,RMVar_hsa_circ_155092,RMVar_hsa_circ_155093,RMVar_hsa_circ_155091 75222 RMVar_ID_75222 Human_SNP_ID_491912607 m1A Human chr12 - 15959914 15959914 15959914 CAAAAGCCACAACACATTTTACCTGATGCCACAGGGATATTACAGCCTGCAGCCTTGAGTGCTTT CAAAAGCCACAACACATTTTACCTGATGCCACGGGGATATTACAGCCTGCAGCCTTGAGTGCTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:15958325..15982405 32194978 MeRIP-seq:(Medium) rs1331112277 Functional Loss SNV dbSNP153 33..33 33 - - - 75223 RMVar_ID_75223 Human_SNP_ID_492006594 m1A Human chr12 - 16347706 16347706 16347706 GGTCCCCTTCTCCCCTCCCAGTACGCACGGTGAGGCCGAGGAGGAGGAAGCAGCAAGCCTGTCCC GGTCCCCTTCTCCCCTCCCAGTACGCACGGTGGGGCCGAGGAGGAGGAAGCAGCAAGCCTGTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:16347640..16347854;chr12:16347672..16347861 26863196 MeRIP-seq:(Medium) rs546045125 Functional Loss SNV dbSNP153 33..33 33 - - - 75224 RMVar_ID_75224 Human_SNP_ID_492009180 m1A Human chr12 + 16357698 16357698 16357698 TTCGAACAGATGACAGAGTAGAACGTGTACGCAGGTAAACCAGTGTCTCTTGAAATTACTTACTT TTCGAACAGATGACAGAGTAGAACGTGTACGCGGGTAAACCAGTGTCTCTTGAAATTACTTACTT A G MGST1 Ensembl:ENSG00000008394 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:16357669..16357747 26863196 MeRIP-seq:(Medium) rs1429286975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755335,Human_RBP_ID_809975,Human_RBP_ID_22757161 Human_Splice_Rec_1343204,Human_Splice_Rec_1343205,Human_Splice_Rec_1343210,Human_Splice_Rec_1343211,Human_Splice_Rec_1343218,Human_Splice_Rec_1343219,Human_Splice_Rec_1343224,Human_Splice_Rec_1343225,Human_Splice_Rec_1343230,Human_Splice_Rec_1343231,Human_Splice_Rec_1343238,Human_Splice_Rec_1343239,Human_Splice_Rec_1343246,Human_Splice_Rec_1343247,Human_Splice_Rec_1343254,Human_Splice_Rec_1343255,Human_Splice_Rec_1343264,Human_Splice_Rec_1343265,Human_Splice_Rec_1343270,Human_Splice_Rec_1343271,Human_Splice_Rec_1343278,Human_Splice_Rec_1343279,Human_Splice_Rec_1343282,Human_Splice_Rec_1343283,Human_Splice_Rec_1343289 RMVar_hsa_circ_310760 75225 RMVar_ID_75225 Human_SNP_ID_492712409 m1A Human chr12 + 19089314 19089314 19089314 GAGGAAGCTTATCTATGAAAAAGCAAAGCACTATCACAAGGAATACAGGCAGATGTACAGAACTG GAGGAAGCTTATCTATGAAAAAGCAAAGCACTGTCACAAGGAATACAGGCAGATGTACAGAACTG A G RPL7P6 Ensembl:ENSG00000227525 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:19089263..19089330 26863196 MeRIP-seq:(Medium) rs183411328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1469189,Human_RBP_ID_5093850,Human_RBP_ID_18527138 Human_miRNA_ID_1891029 75226 RMVar_ID_75226 Human_SNP_ID_492723010 m1A Human chr12 + 19129699 19129699 19129699 TAGGGCGCGCGCGGGGGCGCGCCGGGCCGGGGAGGCGCGCTCGCTCCGCGCTCCCTTCGCTCGCT TAGGGCGCGCGCGGGGGCGCGCCGGGCCGGGGCGGCGCGCTCGCTCCGCGCTCCCTTCGCTCGCT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr12:19129624..19129709;chr12:19129641..19129746 26863410,26863196 MeRIP-seq:(Medium) rs1255679336 Functional Loss SNV dbSNP153 33..33 33 - - - 75227 RMVar_ID_75227 Human_SNP_ID_492723011 m1A Human chr12 + 19129699 19129699 19129699 TAGGGCGCGCGCGGGGGCGCGCCGGGCCGGGGAGGCGCGCTCGCTCCGCGCTCCCTTCGCTCGCT TAGGGCGCGCGCGGGGGCGCGCCGGGCCGGGGGGGCGCGCTCGCTCCGCGCTCCCTTCGCTCGCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr12:19129624..19129709;chr12:19129641..19129746 26863410,26863196 MeRIP-seq:(Medium) rs1255679336 Functional Loss SNV dbSNP153 33..33 33 - - - 75228 RMVar_ID_75228 Human_SNP_ID_492723058 m1A Human chr12 + 19129769 19129769 19129769 CCTCCTCCCTCGGCAGCCGCGGCGGCAGCAGGAGAAGGCGGCGGCGGCGGCTAGGGATCAGACAT CCTCCTCCCTCGGCAGCCGCGGCGGCAGCAGGGGAAGGCGGCGGCGGCGGCTAGGGATCAGACAT A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:19129586..19129809 26863196 MeRIP-seq:(Medium) rs1266048901 Functional Loss SNV dbSNP153 33..33 33 - - - 75229 RMVar_ID_75229 Human_SNP_ID_492723079 m1A Human chr12 + 19129789 19129789 19129789 GGCGGCAGCAGGAGAAGGCGGCGGCGGCGGCTAGGGATCAGACATGGCGGCGGATCTGAACCTGG GGCGGCAGCAGGAGAAGGCGGCGGCGGCGGCTGGGGATCAGACATGGCGGCGGATCTGAACCTGG A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:19129595..19129808 26863196 MeRIP-seq:(Medium) rs755212531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1344139,Human_Splice_Rec_1344145,Human_Splice_Rec_1344207,Human_Splice_Rec_1344255,Human_Splice_Rec_1344305 75230 RMVar_ID_75230 Human_SNP_ID_492723084 m1A Human chr12 + 19129796 19129796 19129796 GCAGGAGAAGGCGGCGGCGGCGGCTAGGGATCAGACATGGCGGCGGATCTGAACCTGGAGTGGAT GCAGGAGAAGGCGGCGGCGGCGGCTAGGGATCGGACATGGCGGCGGATCTGAACCTGGAGTGGAT A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:19129605..19129868 26863196 MeRIP-seq:(Medium) rs1348702845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810040,Human_RBP_ID_9366187 Human_Splice_Rec_1344139,Human_Splice_Rec_1344145,Human_Splice_Rec_1344207,Human_Splice_Rec_1344255,Human_Splice_Rec_1344305 75231 RMVar_ID_75231 Human_SNP_ID_492804291 m1A Human chr12 + 19439950 19439950 19439950 AGTGGGGGGCGGCGAGGCAGAGACGATGTCGGAGCCGAGCCCCGAGAGCGCCAGCCAGGCCGGGG AGTGGGGGGCGGCGAGGCAGAGACGATGTCGGGGCCGAGCCCCGAGAGCGCCAGCCAGGCCGGGG A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:19439849..19439950 26863410 MeRIP-seq:(Medium) rs1245746074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3619,Human_RBP_ID_8725407,Human_RBP_ID_9366192,Human_RBP_ID_22910510 RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 75232 RMVar_ID_75232 Human_SNP_ID_492804311 m1A Human chr12 + 19439989 19439989 19439989 CCCCGAGAGCGCCAGCCAGGCCGGGGAGGACGAAGACGAGGAGGAGGACGACGAGGAGGAGGAAG CCCCGAGAGCGCCAGCCAGGCCGGGGAGGACGGAGACGAGGAGGAGGACGACGAGGAGGAGGAAG A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:19439587..19440263 26863196 MeRIP-seq:(Medium) rs1431627355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34929,Human_RBP_ID_4216321,Human_RBP_ID_5139823,Human_RBP_ID_5560946,Human_RBP_ID_8725407,Human_RBP_ID_9366192,Human_RBP_ID_22910510,Human_RBP_ID_23118041,Human_RBP_ID_24543432,Human_RBP_ID_26321255 RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 75233 RMVar_ID_75233 Human_SNP_ID_492804330 m1A Human chr12 + 19440010 19440008 19440011 CGGGGAGGACGAAGACGAGGAGGAGGACGACGAGGAGGAGGAAGATGAGAGCAGCAGCAGCGGCG CGGGGAGGACGAAGACGAGGAGGAGGACGAC___GAGGAGGAAGATGAGAGCAGCAGCAGCGGCG CGAG C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:19439826..19440400 26863196 MeRIP-seq:(Medium) rs1316377401 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_34929,Human_RBP_ID_874333,Human_RBP_ID_5139565,Human_RBP_ID_8725407,Human_RBP_ID_9366192,Human_RBP_ID_22039182,Human_RBP_ID_22910510,Human_RBP_ID_23118041,Human_RBP_ID_24543432,Human_RBP_ID_26321255,Human_RBP_ID_27806484 RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 75234 RMVar_ID_75234 Human_SNP_ID_492804332 m1A Human chr12 + 19440010 19440010 19440010 CGGGGAGGACGAAGACGAGGAGGAGGACGACGAGGAGGAGGAAGATGAGAGCAGCAGCAGCGGCG CGGGGAGGACGAAGACGAGGAGGAGGACGACGTGGAGGAGGAAGATGAGAGCAGCAGCAGCGGCG A T AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:19439826..19440400 26863196 MeRIP-seq:(Medium) rs986499826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34929,Human_RBP_ID_874333,Human_RBP_ID_5139565,Human_RBP_ID_8725407,Human_RBP_ID_9366192,Human_RBP_ID_22039182,Human_RBP_ID_22910510,Human_RBP_ID_23118041,Human_RBP_ID_24543432,Human_RBP_ID_26321255,Human_RBP_ID_27806484 RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 75235 RMVar_ID_75235 Human_SNP_ID_492809568 m1A Human chr12 - 19457144 19457144 19457144 CAAAATGGATTCCACTGAGCCACCCTACAGCCAGAAGAGATATGAGGAAATTGTTAAGGAAGTCA CAAAATGGATTCCACTGAGCCACCCTACAGCCGGAAGAGATATGAGGAAATTGTTAAGGAAGTCA T C EEF1A1P4 Ensembl:ENSG00000245205 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1245895178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26805494 Human_miRNA_ID_1851216,Human_miRNA_ID_1900424,Human_miRNA_ID_1903010 75236 RMVar_ID_75236 Human_SNP_ID_492823164 m1A Human chr12 - 19503402 19503402 19503402 TCAGTAGCATTTCTATACCCCAATAACACTCAAGCTGACAACCAAATCAAGAATGCAATTCCATT TCAGTAGCATTTCTATACCCCAATAACACTCACGCTGACAACCAAATCAAGAATGCAATTCCATT T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:19503299..19503417 26863196 MeRIP-seq:(Medium) rs1475162565 Functional Loss SNV dbSNP153 33..33 33 - - - 75237 RMVar_ID_75237 Human_SNP_ID_271606977 m1A Human chr6 + 30068639 30068639 30068639 CATCAAACTTCGGAAACGGAAGCCAGAGAAAAAGGTAGAATGGACAAGTGACACTGTGGACAATG CATCAAACTTCGGAAACGGAAGCCAGAGAAAAGGGTAGAATGGACAAGTGACACTGTGGACAATG A G PPP1R11 Ensembl:ENSG00000204619 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30068546..30068644 26863196 MeRIP-seq:(Medium) rs1213902029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15780032 Human_Splice_Rec_748120,Human_Splice_Rec_748121,Human_Splice_Rec_748124,Human_Splice_Rec_748125,Human_Splice_Rec_748130,Human_Splice_Rec_748131,Human_Splice_Rec_748134,Human_Splice_Rec_748135,Human_Splice_Rec_748140,Human_Splice_Rec_748141,Human_Splice_Rec_748143 75238 RMVar_ID_75238 Human_SNP_ID_271607738 m1A Human chr6 + 30071649 30071649 30071649 CCAGTTGTACGCTGCGGCGGTCGGCGGAGATGAGCAGGCGGCGGTGTGCGGTCCCAGGGTCCAGG CCAGTTGTACGCTGCGGCGGTCGGCGGAGATGTGCAGGCGGCGGTGTGCGGTCCCAGGGTCCAGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30071598..30071840 26863196 MeRIP-seq:(Medium) rs1487150697 Functional Loss SNV dbSNP153 33..33 33 - - - 75239 RMVar_ID_75239 Human_SNP_ID_271635048 m1A Human chr6 - 30184775 30184775 30184775 CACAGTTTAACACAAGCTCCCCTGCTCCAGCCAAATTGATCTCCCAGTCTTGTCCTTACCCATTC CACAGTTTAACACAAGCTCCCCTGCTCCAGCCCAATTGATCTCCCAGTCTTGTCCTTACCCATTC T G TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30184726..30184889 26863196 MeRIP-seq:(Medium) rs1241242204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17310166,Human_RBP_ID_17419420,Human_RBP_ID_18862070,Human_RBP_ID_18958064 75240 RMVar_ID_75240 Human_SNP_ID_271635051 m1A Human chr6 - 30184793 30184793 30184793 CCAGGTGCCCCTCATCATCACAGTTTAACACAAGCTCCCCTGCTCCAGCCAAATTGATCTCCCAG CCAGGTGCCCCTCATCATCACAGTTTAACACAGGCTCCCCTGCTCCAGCCAAATTGATCTCCCAG T C TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:30184708..30184925 26863196 MeRIP-seq:(Medium) rs1338404795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590065,Human_RBP_ID_17310166,Human_RBP_ID_17419420,Human_RBP_ID_17535427,Human_RBP_ID_18862070 75241 RMVar_ID_75241 Human_SNP_ID_271635057 m1A Human chr6 - 30184823 30184823 30184823 CTTCTCATTGCCCACGGACCCAACCTCTGTCCAGGTGCCCCTCATCATCACAGTTTAACACAAGC CTTCTCATTGCCCACGGACCCAACCTCTGTCCGGGTGCCCCTCATCATCACAGTTTAACACAAGC T C TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30184676..30184984 26863196 MeRIP-seq:(Medium) rs531736385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17306247,Human_RBP_ID_17419420 Human_miRNA_ID_1091525,Human_miRNA_ID_1152108,Human_miRNA_ID_1161265 75242 RMVar_ID_75242 Human_SNP_ID_271635210 m1A Human chr6 - 30185599 30185599 30185599 GGAGTCCATGAGGGCTCCTTTCCTTTTTGACCACGACCTTGGCCCCAGCTCTGCACTCTCTGGAA GGAGTCCATGAGGGCTCCTTTCCTTTTTGACCGCGACCTTGGCCCCAGCTCTGCACTCTCTGGAA T C TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30185476..30185725 26863196 MeRIP-seq:(Medium) rs1303068620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590071 75243 RMVar_ID_75243 Human_SNP_ID_271635282 m1A Human chr6 - 30185869 30185869 30185869 GAACACGCCTCCTGCTAAGACCCTGAGCCCTGACATCTGCCCCCAGCCCCAACCCTCAGATGCTT GAACACGCCTCCTGCTAAGACCCTGAGCCCTGTCATCTGCCCCCAGCCCCAACCCTCAGATGCTT T A TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30185818..30185940 26863196 MeRIP-seq:(Medium) rs1346367138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3805544,Human_RBP_ID_18072861,Human_RBP_ID_27344921,Human_RBP_ID_27522694 Human_miRNA_ID_829949 75244 RMVar_ID_75244 Human_SNP_ID_271635401 m1A Human chr6 - 30186263 30186263 30186263 GCCGGCTATGGGGATGGATATGACGACTGGGAAACGGACGAAGATGAGGAATCGTTGGGCGATGA GCCGGCTATGGGGATGGATATGACGACTGGGAGACGGACGAAGATGAGGAATCGTTGGGCGATGA T C TRIM26 Ensembl:ENSG00000234127 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:30186144..30186410;chr6:30185701..30186501 26863196 MeRIP-seq:(Medium) rs1305663725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590077,Human_RBP_ID_22106700,Human_RBP_ID_23067773,Human_RBP_ID_23120267,Human_RBP_ID_24554602 75245 RMVar_ID_75245 Human_SNP_ID_271636250 m1A Human chr6 + 30189494 30189494 30189494 GAGAATTCTCCGGTCTTTTTTTTAACCACTCGAGCAATGGGTTTCCCAACCCAGAACTTCTTCCG GAGAATTCTCCGGTCTTTTTTTTAACCACTCGGGCAATGGGTTTCCCAACCCAGAACTTCTTCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30186393..30189519 32194978 MeRIP-seq:(Medium) rs1371947747 Functional Loss SNV dbSNP153 33..33 33 - - - 75246 RMVar_ID_75246 Human_SNP_ID_271637933 m1A Human chr6 - 30196637 30196637 30196637 ACACCTGCTGGAACAGCTGGCGAAGCTGGAGCAGGAGCTCACGGAGGGCAGGGAGAAGTTCAAGA ACACCTGCTGGAACAGCTGGCGAAGCTGGAGCGGGAGCTCACGGAGGGCAGGGAGAAGTTCAAGA T C TRIM26 Ensembl:ENSG00000234127 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30196551..30196750 26863196 MeRIP-seq:(Medium) rs1238408301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590109,Human_RBP_ID_9401745,Human_RBP_ID_23120337 RMVar_hsa_circ_267595 75247 RMVar_ID_75247 Human_SNP_ID_271638445 m1A Human chr6 - 30198760 30198760 30198760 ACACCGAGAGAAGCTGCACTACTACTGTGAGGACGACGGGAAGCTGCTGTGCGTGATGTGCCGGG ACACCGAGAGAAGCTGCACTACTACTGTGAGGGCGACGGGAAGCTGCTGTGCGTGATGTGCCGGG T C TRIM26 Ensembl:ENSG00000234127 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30198710..30198900 26863196 MeRIP-seq:(Medium) rs535534861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1670095,Human_RBP_ID_2017768,Human_RBP_ID_5617727,Human_RBP_ID_7590117,Human_RBP_ID_8641354,Human_RBP_ID_8899585,Human_RBP_ID_18862090 Human_Splice_Rec_748307,Human_Splice_Rec_748325,Human_Splice_Rec_748341,Human_Splice_Rec_748359,Human_Splice_Rec_748365 RMVar_hsa_circ_267595 75248 RMVar_ID_75248 Human_SNP_ID_271638486 m1A Human chr6 + 30198856 30198856 30198856 GGGTCACCTCTCCCGGCTGCCTGCCCTTGTCCACCTTCAGCCGCTCAATGTTCTCCACCAGGCTG GGGTCACCTCTCCCGGCTGCCTGCCCTTGTCCGCCTTCAGCCGCTCAATGTTCTCCACCAGGCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30198666..30199017 26863196 MeRIP-seq:(Medium) rs752486472 Functional Loss SNV dbSNP153 33..33 33 - - - 75249 RMVar_ID_75249 Human_SNP_ID_271641625 m1A Human chr6 - 30213329 30213329 30213329 ACCGCCGTGAGAGAGGAGGGGTGCCGGCCGGGATTCGCGGCCCGGAGCTCGGGACCGGTGAGTAG ACCGCCGTGAGAGAGGAGGGGTGCCGGCCGGGGTTCGCGGCCCGGAGCTCGGGACCGGTGAGTAG T C TRIM26 Ensembl:ENSG00000234127 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30201081..30213425 26863196 MeRIP-seq:(Medium) rs1339964443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4910876,Human_RBP_ID_23138809 Human_Splice_Rec_748319,Human_Splice_Rec_748337,Human_Splice_Rec_748353,Human_Splice_Rec_748363,Human_Splice_Rec_748367,Human_Splice_Rec_748371 75250 RMVar_ID_75250 Human_SNP_ID_271665151 m1A Human chr6 - 30326756 30326756 30326756 AGGGCTGGCGATGAGAAGCAGCAGGGGGAATCAAGGGCAAGAAGGGACCCAGAGGGGCAGGTGGC AGGGCTGGCGATGAGAAGCAGCAGGGGGAATCTAGGGCAAGAAGGGACCCAGAGGGGCAGGTGGC T A HCG18 Ensembl:ENSG00000231074 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30326446..30327072 26863196 MeRIP-seq:(Medium) rs1003825089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792428,Human_RBP_ID_840673,Human_RBP_ID_1069571,Human_RBP_ID_3822942,Human_RBP_ID_5217214,Human_RBP_ID_5656504,Human_RBP_ID_8944001,Human_RBP_ID_9437383,Human_RBP_ID_18425381,Human_RBP_ID_26353555 75251 RMVar_ID_75251 Human_SNP_ID_271665395 m1A Human chr6 + 30327440 30327440 30327440 CGGGGGTGGGACAGAGTTGTGGACAACCTCTCAGGAGAGGGTCGCAAGGTGGGACCCTGAACAGT CGGGGGTGGGACAGAGTTGTGGACAACCTCTCGGGAGAGGGTCGCAAGGTGGGACCCTGAACAGT A G TRIM39 Ensembl:ENSG00000204599 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30327412..30327537 32194978 MeRIP-seq:(Medium) rs1000247515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949139 75252 RMVar_ID_75252 Human_SNP_ID_271669394 m1A Human chr6 + 30345431 30345421 30345432 GTGAGACAGCCACGGGGCGGGCGGCGGGCGGGACGCGGGAGGAACGCGAGAGGGAGCGCGGGCGC GTGAGACAGCCACGGGGCGGGCG___________GCGGGAGGAACGCGAGAGGGAGCGCGGGCGC GGCGGGCGGGAC G TRIM39-RPP21,RPP21 Ensembl:ENSG00000248167,Ensembl:ENSG00000241370 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:30345422..30345520 26863410 MeRIP-seq:(Medium) rs147085011 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_949143,Human_RBP_ID_5400243,Human_RBP_ID_19130312,Human_RBP_ID_22553553 75253 RMVar_ID_75253 Human_SNP_ID_271669401 m1A Human chr6 + 30345431 30345431 30345431 GTGAGACAGCCACGGGGCGGGCGGCGGGCGGGACGCGGGAGGAACGCGAGAGGGAGCGCGGGCGC GTGAGACAGCCACGGGGCGGGCGGCGGGCGGGCCGCGGGAGGAACGCGAGAGGGAGCGCGGGCGC A C TRIM39-RPP21,RPP21 Ensembl:ENSG00000248167,Ensembl:ENSG00000241370 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:30345422..30345520 26863410 MeRIP-seq:(Medium) rs768423593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949143,Human_RBP_ID_5400243,Human_RBP_ID_19130312,Human_RBP_ID_22553553 75254 RMVar_ID_75254 Human_SNP_ID_271669476 m1A Human chr6 - 30345555 30345555 30345555 GTTGGAGCACTCACGTCTCTGGCGCTGGGTGCAGGTGAGGCCCGGGACGAGGAGGGAAGAGCAGC GTTGGAGCACTCACGTCTCTGGCGCTGGGTGCTGGTGAGGCCCGGGACGAGGAGGGAAGAGCAGC T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30345179..30345575 32194978 MeRIP-seq:(Medium) rs890849504 Functional Loss SNV dbSNP153 33..33 33 - - - 75255 RMVar_ID_75255 Human_SNP_ID_271669744 m1A Human chr6 + 30346534 30346534 30346534 TCCCGGGCATTTACTCTGGGGAGACAGGCCTGAGGCCCAGCTCGGGAGCCAAGCAGGTGAGAGGT TCCCGGGCATTTACTCTGGGGAGACAGGCCTGCGGCCCAGCTCGGGAGCCAAGCAGGTGAGAGGT A C TRIM39-RPP21,RPP21 Ensembl:ENSG00000248167,Ensembl:ENSG00000241370 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30346443..30346738 32194978 MeRIP-seq:(Medium) rs375598004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252765,Human_RBP_ID_791608,Human_RBP_ID_17663244,Human_RBP_ID_18195359,Human_RBP_ID_19017859,Human_RBP_ID_19128731,Human_RBP_ID_22461016,Human_RBP_ID_26828113 Human_Splice_Rec_748729,Human_Splice_Rec_748737,Human_Splice_Rec_748747,Human_Splice_Rec_748753,Human_Splice_Rec_748759,Human_Splice_Rec_748765,Human_Splice_Rec_748773,Human_Splice_Rec_748779,Human_Splice_Rec_748787 75256 RMVar_ID_75256 Human_SNP_ID_271703386 m1A Human chr6 - 30489794 30489794 30489794 CACGAACTGGGTGTCGTCCACGTAGCCCACAGAGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGG CACGAACTGGGTGTCGTCCACGTAGCCCACAGTGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30489743..30489950 26863196 MeRIP-seq:(Medium) rs758258520 Functional Loss SNV dbSNP153 33..33 33 - - - 75257 RMVar_ID_75257 Human_SNP_ID_271703387 m1A Human chr6 - 30489794 30489794 30489794 CACGAACTGGGTGTCGTCCACGTAGCCCACAGAGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGG CACGAACTGGGTGTCGTCCACGTAGCCCACAGCGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30489743..30489950 26863196 MeRIP-seq:(Medium) rs758258520 Functional Loss SNV dbSNP153 33..33 33 - - - 75258 RMVar_ID_75258 Human_SNP_ID_271703421 m1A Human chr6 - 30489893 30489893 30489893 GGCGCTCCGTGTCTCCCGGTCCCAATACTCTGACCCCTCCTGCTCCATCCACGGCGCCCGCGGCA GGCGCTCCGTGTCTCCCGGTCCCAATACTCTGGCCCCTCCTGCTCCATCCACGGCGCCCGCGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30489726..30490028 26863196 MeRIP-seq:(Medium) rs774752159 Functional Loss SNV dbSNP153 33..33 33 - - - 75259 RMVar_ID_75259 Human_SNP_ID_271703422 m1A Human chr6 - 30489893 30489893 30489893 GGCGCTCCGTGTCTCCCGGTCCCAATACTCTGACCCCTCCTGCTCCATCCACGGCGCCCGCGGCA GGCGCTCCGTGTCTCCCGGTCCCAATACTCTGCCCCCTCCTGCTCCATCCACGGCGCCCGCGGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30489726..30490028 26863196 MeRIP-seq:(Medium) rs774752159 Functional Loss SNV dbSNP153 33..33 33 - - - 75260 RMVar_ID_75260 Human_SNP_ID_271703592 m1A Human chr6 - 30490412 30490411 30490412 TAGGCTCTCTGGTGCTCCGCCTCAGAGGCATCATTTGACTTTTGCTCGGAGATCTGAGCCGCCGT TAGGCTCTCTGGTGCTCCGCCTCAGAGGCATC_TTTGACTTTTGCTCGGAGATCTGAGCCGCCGT AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30490363..30490446 26863196 MeRIP-seq:(Medium) rs1378836078 Functional Loss DEL dbSNP153 33..33 33 - - - 75261 RMVar_ID_75261 Human_SNP_ID_271704170 m1A Human chr6 - 30492528 30492528 30492528 CCCCTGGGCACTGTCGCTCCCTGGGGTAGAACAAAAACAAGACCTGGTCAGAGCCCACAGGAGAT CCCCTGGGCACTGTCGCTCCCTGGGGTAGAACCAAAACAAGACCTGGTCAGAGCCCACAGGAGAT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30492526..30492575 32194978 MeRIP-seq:(Medium) rs372286418 Functional Loss SNV dbSNP153 33..33 33 - - - 75262 RMVar_ID_75262 Human_SNP_ID_271704484 m1A Human chr6 + 30493975 30493975 30493975 AACCCATTCGAGCAGCCACGTAGGCTGCACCCAGCAAAGCCACAGGCACGGGGCTACCTGAGGCC AACCCATTCGAGCAGCCACGTAGGCTGCACCCGGCAAAGCCACAGGCACGGGGCTACCTGAGGCC A G HLA-E Ensembl:ENSG00000204592 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30493926..30494100 32194978 MeRIP-seq:(Medium) rs777079808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8215947 75263 RMVar_ID_75263 Human_SNP_ID_271704485 m1A Human chr6 + 30493975 30493975 30493975 AACCCATTCGAGCAGCCACGTAGGCTGCACCCAGCAAAGCCACAGGCACGGGGCTACCTGAGGCC AACCCATTCGAGCAGCCACGTAGGCTGCACCCTGCAAAGCCACAGGCACGGGGCTACCTGAGGCC A T HLA-E Ensembl:ENSG00000204592 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30493926..30494100 32194978 MeRIP-seq:(Medium) rs777079808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8215947 75264 RMVar_ID_75264 Human_SNP_ID_271716388 m1A Human chr6 - 30546192 30546192 30546192 GAAGAGCTGAGCAGCTCCTGTGAGGAGGAGGGAGAGGAGGACCGGGATGCGGATGAGGAGGGAGA GAAGAGCTGAGCAGCTCCTGTGAGGAGGAGGGTGAGGAGGACCGGGATGCGGATGAGGAGGGAGA T A GNL1 Ensembl:ENSG00000204590 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30546001..30546545 32194978 MeRIP-seq:(Medium) rs369257124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252667,Human_RBP_ID_4878979,Human_RBP_ID_5532334,Human_RBP_ID_7590829,Human_RBP_ID_23067496,Human_RBP_ID_24156167 Human_miRNA_ID_1192566 75265 RMVar_ID_75265 Human_SNP_ID_271716389 m1A Human chr6 - 30546196 30546193 30546196 AGAGGAAGAGCTGAGCAGCTCCTGTGAGGAGGAGGGAGAGGAGGACCGGGATGCGGATGAGGAGG AGAGGAAGAGCTGAGCAGCTCCTGTGAGGAGG___GAGAGGAGGACCGGGATGCGGATGAGGAGG CCCT C GNL1 Ensembl:ENSG00000204590 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:30546161..30546243 26863410 MeRIP-seq:(Medium) rs765976450 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_252667,Human_RBP_ID_5532334,Human_RBP_ID_7590829,Human_RBP_ID_23067496,Human_RBP_ID_24156167 Human_miRNA_ID_1192566 75266 RMVar_ID_75266 Human_SNP_ID_271716646 m1A Human chr6 - 30547203 30547203 30547203 CCCTACACTGCTGTGGGCTACCTGGCCTCCCGAATTCCCGTGCAGGCCCTGCTCCACCTGCGCCA CCCTACACTGCTGTGGGCTACCTGGCCTCCCGCATTCCCGTGCAGGCCCTGCTCCACCTGCGCCA T G GNL1 Ensembl:ENSG00000204590 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30547089..30547349 26863196 MeRIP-seq:(Medium) rs376823821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660709,Human_RBP_ID_8905161,Human_RBP_ID_18073025,Human_RBP_ID_18862222,Human_RBP_ID_19017860,Human_RBP_ID_22461781 Human_Splice_Rec_748838,Human_Splice_Rec_748839,Human_Splice_Rec_748846,Human_Splice_Rec_748847,Human_Splice_Rec_748850 75267 RMVar_ID_75267 Human_SNP_ID_271716754 m1A Human chr6 + 30547528 30547528 30547528 ATTGATCAGCGAGGACTTTCCCACATTAGGGAAACCTGAGGAAGGCAAGGAAAATTAACGTTTAA ATTGATCAGCGAGGACTTTCCCACATTAGGGACACCTGAGGAAGGCAAGGAAAATTAACGTTTAA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:30547496..30547597 26863410 MeRIP-seq:(Medium) rs750641188 Functional Loss SNV dbSNP153 33..33 33 - - - 75268 RMVar_ID_75268 Human_SNP_ID_271716877 m1A Human chr6 - 30548252 30548252 30548252 GCCAGAAACACAAAAACTGGTGGTGGTGAGTGAGCAGAGTGGCAGTGAGCCCCAAGGCTTCCAGT GCCAGAAACACAAAAACTGGTGGTGGTGAGTGGGCAGAGTGGCAGTGAGCCCCAAGGCTTCCAGT T C GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:30548249..30548401;chr6:30548250..30548640 26863196 MeRIP-seq:(Medium) rs1562703790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782316,Human_RBP_ID_24156178 75269 RMVar_ID_75269 Human_SNP_ID_271717268 m1A Human chr6 + 30550173 30550173 30550173 AAATACCACTTATATCCATCAATGGTTCCCCAAATTTAAATCTTTCCCAAATTCAAATTTCCGTC AAATACCACTTATATCCATCAATGGTTCCCCATATTTAAATCTTTCCCAAATTCAAATTTCCGTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30550170..30550581 26863196 MeRIP-seq:(Medium) rs1283420720 Functional Loss SNV dbSNP153 33..33 33 - - - 75270 RMVar_ID_75270 Human_SNP_ID_271717383 m1A Human chr6 - 30550794 30550794 30550794 AGGACCAGCAAGAGTGCCCAGGGGATTGGAGTATGGGAGCCAGGATAAAGTACTGGGGATGAGGT AGGACCAGCAAGAGTGCCCAGGGGATTGGAGTCTGGGAGCCAGGATAAAGTACTGGGGATGAGGT T G GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:30550792..30550927;chr6:30550783..30550948 26863196 MeRIP-seq:(Medium) rs1165324595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590848,Human_RBP_ID_17198768 75271 RMVar_ID_75271 Human_SNP_ID_271717389 m1A Human chr6 - 30550816 30550816 30550816 AGGGAACGGGCTTGGAGATTCTAGGACCAGCAAGAGTGCCCAGGGGATTGGAGTATGGGAGCCAG AGGGAACGGGCTTGGAGATTCTAGGACCAGCATGAGTGCCCAGGGGATTGGAGTATGGGAGCCAG T A GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30550814..30550900 26863196 MeRIP-seq:(Medium) rs1466485138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7590848,Human_RBP_ID_17198768 75272 RMVar_ID_75272 Human_SNP_ID_271718406 m1A Human chr6 + 30555087 30555087 30555087 CTGAGCCAGGCTGATACACCTCCCGGATGTCCAGCTCCAACAACTCAGCACTGACCGGCTGTAGA CTGAGCCAGGCTGATACACCTCCCGGATGTCCTGCTCCAACAACTCAGCACTGACCGGCTGTAGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30553351..30555125 32194978 MeRIP-seq:(Medium) rs1242848775 Functional Loss SNV dbSNP153 33..33 33 - - - 75273 RMVar_ID_75273 Human_SNP_ID_271718591 m1A Human chr6 - 30555688 30555688 30555688 GGCTTCAAGATGGGCTGCGCTCCAGTTCCAACAGCCGCAGCGGGAGCCGGGAGCGGCGAGAGGAA GGCTTCAAGATGGGCTGCGCTCCAGTTCCAACTGCCGCAGCGGGAGCCGGGAGCGGCGAGAGGAA T A GNL1 Ensembl:ENSG00000204590 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30554815..30555883 26863196 MeRIP-seq:(Medium) rs781607988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949150,Human_RBP_ID_3969612,Human_RBP_ID_5327088,Human_RBP_ID_18862234,Human_RBP_ID_19016495,Human_RBP_ID_22616057,Human_RBP_ID_23067497,Human_RBP_ID_26353559 Human_Splice_Rec_748822 75274 RMVar_ID_75274 Human_SNP_ID_271718729 m1A Human chr6 + 30556083 30556083 30556083 CAGAGGTGCAGCGGGCACACCCCTCCTTCCAGATGTGCGGAAGCCCGAGCCCCGCCCCCTCCTCC CAGAGGTGCAGCGGGCACACCCCTCCTTCCAGCTGTGCGGAAGCCCGAGCCCCGCCCCCTCCTCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30556082..30556275 32194978 MeRIP-seq:(Medium) rs1188306278 Functional Loss SNV dbSNP153 33..33 33 - - - 75275 RMVar_ID_75275 Human_SNP_ID_271718730 m1A Human chr6 - 30556084 30556084 30556084 GGGAGGAGGGGGCGGGGCTCGGGCTTCCGCACATCTGGAAGGAGGGGTGTGCCCGCTGCACCTCT GGGAGGAGGGGGCGGGGCTCGGGCTTCCGCACTTCTGGAAGGAGGGGTGTGCCCGCTGCACCTCT T A GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30556082..30556724 32194978 MeRIP-seq:(Medium) rs559715683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5397940,Human_RBP_ID_19128740 75276 RMVar_ID_75276 Human_SNP_ID_271718731 m1A Human chr6 - 30556084 30556084 30556084 GGGAGGAGGGGGCGGGGCTCGGGCTTCCGCACATCTGGAAGGAGGGGTGTGCCCGCTGCACCTCT GGGAGGAGGGGGCGGGGCTCGGGCTTCCGCACGTCTGGAAGGAGGGGTGTGCCCGCTGCACCTCT T C GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30556082..30556724 32194978 MeRIP-seq:(Medium) rs559715683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5397940,Human_RBP_ID_19128740 75277 RMVar_ID_75277 Human_SNP_ID_271718889 m1A Human chr6 + 30556451 30556451 30556451 GGATGATGCGGGGTGGGCTACTGGCACGTGAGAGCCAGTGGCACCGAGAGGGCGCCCCGGCGGCG GGATGATGCGGGGTGGGCTACTGGCACGTGAGGGCCAGTGGCACCGAGAGGGCGCCCCGGCGGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:30556159..30556624 26863410 MeRIP-seq:(Medium) rs1280357015 Functional Loss SNV dbSNP153 33..33 33 - - - 75278 RMVar_ID_75278 Human_SNP_ID_271719205 m1A Human chr6 + 30557352 30557352 30557352 CGCTGCAGCCATTGCCGCAGACACGATGCCGAAACGAAAGAAGCAGAATCATCACCAGCCACCGA CGCTGCAGCCATTGCCGCAGACACGATGCCGAGACGAAAGAAGCAGAATCATCACCAGCCACCGA A G PRR3 Ensembl:ENSG00000204576 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30557301..30557483 26863196 MeRIP-seq:(Medium) rs951442652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1670247,Human_RBP_ID_8641516,Human_RBP_ID_18862239 Human_Splice_Rec_748861,Human_Splice_Rec_748865,Human_Splice_Rec_748871,Human_Splice_Rec_748877,Human_Splice_Rec_748885 75279 RMVar_ID_75279 Human_SNP_ID_271719241 m1A Human chr6 + 30557425 30557425 30557425 CAGCCCCCGCTGCCCGAGCGGGAAGAGACTGGAGATGAGGAGGATGGGAGTCCCATCGGTGAGGG CAGCCCCCGCTGCCCGAGCGGGAAGAGACTGGCGATGAGGAGGATGGGAGTCCCATCGGTGAGGG A C PRR3 Ensembl:ENSG00000204576 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:30557324..30557450 26863196 MeRIP-seq:(Medium) rs1393049265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251850,Human_RBP_ID_7590865,Human_RBP_ID_8641517,Human_RBP_ID_19130323 Human_Splice_Rec_748861,Human_Splice_Rec_748865,Human_Splice_Rec_748871,Human_Splice_Rec_748877,Human_Splice_Rec_748885 Human_miRNA_ID_1564691 75280 RMVar_ID_75280 Human_SNP_ID_271722273 m1A Human chr6 + 30570939 30570939 30570939 CGCGCCCCATGACCCTCTCCTAAAACACGCGCAGTCTCCTCTCTCTTCCCCTTCCTCTCGTGTCT CGCGCCCCATGACCCTCTCCTAAAACACGCGCCGTCTCCTCTCTCTTCCCCTTCCTCTCGTGTCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30570823..30570991 26863196 MeRIP-seq:(Medium) rs1253650331 Functional Loss SNV dbSNP153 33..33 33 - - - 75281 RMVar_ID_75281 Human_SNP_ID_271722509 m1A Human chr6 + 30571556 30571556 30571556 GAGTGGATCGGGGACGGAGAGAGCACGAGCCCATCAGGTGAGGCTGGTAGGCAAGGAAGAAACGA GAGTGGATCGGGGACGGAGAGAGCACGAGCCCGTCAGGTGAGGCTGGTAGGCAAGGAAGAAACGA A G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30571524..30577884 32194978 MeRIP-seq:(Medium) rs1318349203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903799,Human_RBP_ID_7590966,Human_RBP_ID_24387629,Human_RBP_ID_24548360 Human_Splice_Rec_748889,Human_Splice_Rec_748935,Human_Splice_Rec_748955,Human_Splice_Rec_748967 75282 RMVar_ID_75282 Human_SNP_ID_271722510 m1A Human chr6 + 30571556 30571556 30571556 GAGTGGATCGGGGACGGAGAGAGCACGAGCCCATCAGGTGAGGCTGGTAGGCAAGGAAGAAACGA GAGTGGATCGGGGACGGAGAGAGCACGAGCCCTTCAGGTGAGGCTGGTAGGCAAGGAAGAAACGA A T ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30571524..30577884 32194978 MeRIP-seq:(Medium) rs1318349203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903799,Human_RBP_ID_7590966,Human_RBP_ID_24387629,Human_RBP_ID_24548360 Human_Splice_Rec_748889,Human_Splice_Rec_748935,Human_Splice_Rec_748955,Human_Splice_Rec_748967 75283 RMVar_ID_75283 Human_SNP_ID_271722965 m1A Human chr6 + 30573536 30573536 30573536 CAGATTGAACCAAAAAGAAGGTTAAAGGTGGGAACCCTAAAGAACTTCAGCAATTGCAGGAAGCA CAGATTGAACCAAAAAGAAGGTTAAAGGTGGGTACCCTAAAGAACTTCAGCAATTGCAGGAAGCA A T ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30573533..30573717 26863196 MeRIP-seq:(Medium) rs939358526 Functional Loss SNV dbSNP153 33..33 33 - - - 75284 RMVar_ID_75284 Human_SNP_ID_271723862 m1A Human chr6 + 30577421 30577421 30577421 ATGTCCGCTTAACTTTCTAGACAAAGTGGTGAAGAAAGGGAAGAAGGACAAGAAGATCAAAAAAA ATGTCCGCTTAACTTTCTAGACAAAGTGGTGATGAAAGGGAAGAAGGACAAGAAGATCAAAAAAA A T ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:30577401..30577475 26863196 MeRIP-seq:(Medium) rs1188483266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4910980,Human_RBP_ID_5617731,Human_RBP_ID_7590999,Human_RBP_ID_23068829,Human_RBP_ID_24548361,Human_RBP_ID_26354845 Human_Splice_Rec_748890,Human_Splice_Rec_748891,Human_Splice_Rec_748936,Human_Splice_Rec_748937,Human_Splice_Rec_748968,Human_Splice_Rec_748969 75285 RMVar_ID_75285 Human_SNP_ID_271723974 m1A Human chr6 + 30577882 30577882 30577882 GGCTGGGGAAGAAGAGAAAGTGCTCAAGGAGAAGGAGCAGCAGCAGCAGCAACAGCAACAGCAGG GGCTGGGGAAGAAGAGAAAGTGCTCAAGGAGAGGGAGCAGCAGCAGCAGCAACAGCAACAGCAGG A G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:30577801..30578110 26863196 MeRIP-seq:(Medium) rs1404226235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5152061,Human_RBP_ID_8237584,Human_RBP_ID_9400173,Human_RBP_ID_18413831,Human_RBP_ID_23059755,Human_RBP_ID_24178818,Human_RBP_ID_24548363,Human_RBP_ID_26353140,Human_RBP_ID_27827422 Human_Splice_Rec_748892,Human_Splice_Rec_748893,Human_Splice_Rec_748938,Human_Splice_Rec_748939,Human_Splice_Rec_748956,Human_Splice_Rec_748957,Human_Splice_Rec_748970,Human_Splice_Rec_748971 75286 RMVar_ID_75286 Human_SNP_ID_271724099 m1A Human chr6 + 30578191 30578189 30578192 TCTTAAGAAGCTCTCAGTGCCAACCAGTGATGAGGAGGATGAAGGTAAATGACCTGAGGGGGAAT TCTTAAGAAGCTCTCAGTGCCAACCAGTGAT___GAGGATGAAGGTAAATGACCTGAGGGGGAAT TGAG T ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30578142..30578387 32194978 MeRIP-seq:(Medium) rs756580530 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2017993,Human_RBP_ID_7591003,Human_RBP_ID_9350419,Human_RBP_ID_19130327,Human_RBP_ID_24178819,Human_RBP_ID_24548672,Human_RBP_ID_24554604,Human_RBP_ID_26353142,Human_RBP_ID_27827424 Human_Splice_Rec_748895,Human_Splice_Rec_748941,Human_Splice_Rec_748959,Human_Splice_Rec_748973,Human_Splice_Rec_749015 75287 RMVar_ID_75287 Human_SNP_ID_271724215 m1A Human chr6 + 30578519 30578508 30578520 AGCCCTGATTCAGGATCAGAGTGAGGAAGAGGAGGAGGAAGAAAAACATCCTCCTAAGCCTGCCA AGCCCTGATTCAGGATCAGAGT____________GAGGAAGAAAAACATCCTCCTAAGCCTGCCA TGAGGAAGAGGAG T ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:30578404..30578609;chr6:30578326..30578627 26863196 MeRIP-seq:(Medium) rs777372626 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_791782,Human_RBP_ID_1670291,Human_RBP_ID_2017994,Human_RBP_ID_3002712,Human_RBP_ID_7591005,Human_RBP_ID_9309550,Human_RBP_ID_9341596,Human_RBP_ID_9400177,Human_RBP_ID_18862271,Human_RBP_ID_19128746,Human_RBP_ID_22010744,Human_RBP_ID_24548366,Human_RBP_ID_26353567,Human_RBP_ID_27827426 Human_Splice_Rec_748898,Human_Splice_Rec_748899,Human_Splice_Rec_748944,Human_Splice_Rec_748945,Human_Splice_Rec_748962,Human_Splice_Rec_748963,Human_Splice_Rec_748976,Human_Splice_Rec_748977 75288 RMVar_ID_75288 Human_SNP_ID_271724610 m1A Human chr6 - 30580007 30580006 30580007 CCCCAATACCTCCTCCTGCTAGTTACTCTCTCACCTTAGCCTTCCCTTTTGACTTCTCTTCCTTT CCCCAATACCTCCTCCTGCTAGTTACTCTCTC_CCTTAGCCTTCCCTTTTGACTTCTCTTCCTTT GT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30579926..30580025 26863196 MeRIP-seq:(Medium) rs780573759 Functional Loss DEL dbSNP153 33..33 33 - - - 75289 RMVar_ID_75289 Human_SNP_ID_271724790 m1A Human chr6 + 30580499 30580496 30580499 AGGAAAAGGAGCCTCCCAAACAAGGGAAGGAGAAGGCCAAGAAGGCAGAGCAGGTGTGTATTTGG AGGAAAAGGAGCCTCCCAAACAAGGGAAGG___AGGCCAAGAAGGCAGAGCAGGTGTGTATTTGG GAGA G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30580361..30580575 26863196 MeRIP-seq:(Medium) rs1198223445 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_841607,Human_RBP_ID_9400181,Human_RBP_ID_24548368,Human_RBP_ID_26353570,Human_RBP_ID_26771899,Human_RBP_ID_27827428 Human_Splice_Rec_748902,Human_Splice_Rec_748903,Human_Splice_Rec_748948,Human_Splice_Rec_748949,Human_Splice_Rec_748966,Human_Splice_Rec_748980,Human_Splice_Rec_748981 Human_miRNA_ID_2394815,Human_miRNA_ID_2906953,Human_miRNA_ID_3025785 RMVar_hsa_circ_373943,RMVar_hsa_circ_237808 75290 RMVar_ID_75290 Human_SNP_ID_271725229 m1A Human chr6 + 30582352 30582352 30582352 TGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCAGGAGTCCCTAGTTTTGACCATCCCCGGG TGCTGGGATTACAGGCGTGAGCCACCGCGCCCCGCCAGGAGTCCCTAGTTTTGACCATCCCCGGG A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30582345..30582525 26863196 MeRIP-seq:(Medium) rs777655820 Functional Loss SNV dbSNP153 33..33 33 - - - 75291 RMVar_ID_75291 Human_SNP_ID_271725278 m1A Human chr6 + 30582475 30582475 30582475 AGTCTAAGGCAGATGATCCCTATGCTCATCTTAGCAAAAAGGAGAAGAAAAAGCTGAAAAAACAG AGTCTAAGGCAGATGATCCCTATGCTCATCTTGGCAAAAAGGAGAAGAAAAAGCTGAAAAAACAG A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30582426..30582525 32194978 MeRIP-seq:(Medium) rs1435229987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660784,Human_RBP_ID_948567,Human_RBP_ID_1046569,Human_RBP_ID_4879198,Human_RBP_ID_8237334,Human_RBP_ID_9341572,Human_RBP_ID_9350421,Human_RBP_ID_9400182,Human_RBP_ID_17663246,Human_RBP_ID_18413834,Human_RBP_ID_18544931,Human_RBP_ID_19016497,Human_RBP_ID_24548370,Human_RBP_ID_26353143,Human_RBP_ID_27827429 Human_Splice_Rec_748950,Human_Splice_Rec_748951,Human_Splice_Rec_748982,Human_Splice_Rec_748983,Human_Splice_Rec_749017 75292 RMVar_ID_75292 Human_SNP_ID_271725279 m1A Human chr6 + 30582475 30582475 30582475 AGTCTAAGGCAGATGATCCCTATGCTCATCTTAGCAAAAAGGAGAAGAAAAAGCTGAAAAAACAG AGTCTAAGGCAGATGATCCCTATGCTCATCTTCGCAAAAAGGAGAAGAAAAAGCTGAAAAAACAG A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30582426..30582525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_660784,Human_RBP_ID_948567,Human_RBP_ID_1046569,Human_RBP_ID_4879198,Human_RBP_ID_8237334,Human_RBP_ID_9341572,Human_RBP_ID_9350421,Human_RBP_ID_9400182,Human_RBP_ID_17663246,Human_RBP_ID_18413834,Human_RBP_ID_18544931,Human_RBP_ID_19016497,Human_RBP_ID_24548370,Human_RBP_ID_26353143,Human_RBP_ID_27827429 Human_Splice_Rec_748950,Human_Splice_Rec_748951,Human_Splice_Rec_748982,Human_Splice_Rec_748983,Human_Splice_Rec_749017 75293 RMVar_ID_75293 Human_SNP_ID_271725622 m1A Human chr6 + 30583806 30583806 30583806 TGGCCAGGTCCTAATAGCTTTTATTCCCCAGCAAGGGCAAGACCACACTCCTCAAGCACATTGCC TGGCCAGGTCCTAATAGCTTTTATTCCCCAGCCAGGGCAAGACCACACTCCTCAAGCACATTGCC A C ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30579987..30585310 32194978 MeRIP-seq:(Medium) rs748174962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046571,Human_RBP_ID_2018007,Human_RBP_ID_5398519,Human_RBP_ID_22682474 Human_Splice_Rec_748908,Human_Splice_Rec_748909,Human_Splice_Rec_748988,Human_Splice_Rec_748989,Human_Splice_Rec_749022,Human_Splice_Rec_749023 Human_miRNA_ID_1960299,Human_miRNA_ID_1960300,Human_miRNA_ID_1960301,Human_miRNA_ID_2610965,Human_miRNA_ID_2610966,Human_miRNA_ID_2610967,Human_miRNA_ID_2909954,Human_miRNA_ID_2909955,Human_miRNA_ID_2909956 RMVar_hsa_circ_92850,RMVar_hsa_circ_109665,RMVar_hsa_circ_237809,RMVar_hsa_circ_237810 75294 RMVar_ID_75294 Human_SNP_ID_271725757 m1A Human chr6 + 30584303 30584303 30584303 GCGGCGGCTTCAGGGACAGCTGGAACAAGGGGATGACACAGCTGCTGAGAGGCTAGAGAAGGTAG GCGGCGGCTTCAGGGACAGCTGGAACAAGGGGTTGACACAGCTGCTGAGAGGCTAGAGAAGGTAG A T ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30584176..30584500 26863196 MeRIP-seq:(Medium) rs1239367154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789513,Human_RBP_ID_3969615,Human_RBP_ID_7591026,Human_RBP_ID_18085197,Human_RBP_ID_19017873,Human_RBP_ID_22618104 Human_Splice_Rec_748911,Human_Splice_Rec_748991,Human_Splice_Rec_749025 RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 75295 RMVar_ID_75295 Human_SNP_ID_271725758 m1A Human chr6 - 30584313 30584313 30584313 GCCATCTCCTCTACCTTCTCTAGCCTCTCAGCAGCTGTGTCATCCCCTTGTTCCAGCTGTCCCTG GCCATCTCCTCTACCTTCTCTAGCCTCTCAGCCGCTGTGTCATCCCCTTGTTCCAGCTGTCCCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30584201..30584450 26863196 MeRIP-seq:(Medium) rs1304710690 Functional Loss SNV dbSNP153 33..33 33 - - - 75296 RMVar_ID_75296 Human_SNP_ID_271727463 m1A Human chr6 + 30590646 30590646 30590646 TAGCCAAATCGATGGTGACTTTGAAGACTACAAGCGGGAGGTGTTGGAGGCCCTGGGTGAAGTCA TAGCCAAATCGATGGTGACTTTGAAGACTACAGGCGGGAGGTGTTGGAGGCCCTGGGTGAAGTCA A G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30590596..30590756 26863196 MeRIP-seq:(Medium) rs780347494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1670327,Human_RBP_ID_2018031,Human_RBP_ID_3805753,Human_RBP_ID_5121864,Human_RBP_ID_7591057,Human_RBP_ID_8237335,Human_RBP_ID_9309558,Human_RBP_ID_22104794,Human_RBP_ID_22310595,Human_RBP_ID_22461021,Human_RBP_ID_23215119,Human_RBP_ID_27345058 Human_miRNA_ID_209108 75297 RMVar_ID_75297 Human_SNP_ID_271727484 m1A Human chr6 + 30590701 30590700 30590701 GGTGAAGTCATGGTCAGCCGGCCCCGAGAGTGAGCTTTCCTTCCCAGAAGTCTCCCGAGAGACAT GGTGAAGTCATGGTCAGCCGGCCCCGAGAGTG_GCTTTCCTTCCCAGAAGTCTCCCGAGAGACAT GA G ABCF1 Ensembl:ENSG00000204574 Protein coding stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30590651..30590700 32194978 MeRIP-seq:(Medium) rs76018112 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1670330,Human_RBP_ID_2018032,Human_RBP_ID_22106704 75298 RMVar_ID_75298 Human_SNP_ID_271730777 m1A Human chr6 - 30602295 30602295 30602295 CGGTGGCATGGGAAGTGGGCATCGCCCCCATGAAGGCCCTGGTGGTAGCATGGGTGGGGGTGGAG CGGTGGCATGGGAAGTGGGCATCGCCCCCATGGAGGCCCTGGTGGTAGCATGGGTGGGGGTGGAG T C PPP1R10 Ensembl:ENSG00000204569 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30602212..30602323 32194978 MeRIP-seq:(Medium) rs1456053007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9309562,Human_RBP_ID_9354684,Human_RBP_ID_18450080 Human_miRNA_ID_1195949 75299 RMVar_ID_75299 Human_SNP_ID_271735012 m1A Human chr6 - 30616907 30616905 30616907 CAACATCTAAGCCCTTGAAAGGATCCTGAGAGAGGGGGGAAAGGGAAAACAGCAGCCACCAGCCC CAACATCTAAGCCCTTGAAAGGATCCTGAGAG__GGGGGAAAGGGAAAACAGCAGCCACCAGCCC CCT C PPP1R10 Ensembl:ENSG00000204569 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30616857..30616958 26863196 MeRIP-seq:(Medium) rs769501719 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_947418,Human_RBP_ID_1670404,Human_RBP_ID_3002800,Human_RBP_ID_15783572,Human_RBP_ID_18862355,Human_RBP_ID_22104807,Human_RBP_ID_23120272,Human_RBP_ID_26353591 Human_Splice_Rec_749058,Human_Splice_Rec_749108,Human_Splice_Rec_749114 75300 RMVar_ID_75300 Human_SNP_ID_271735014 m1A Human chr6 - 30616907 30616907 30616907 CAACATCTAAGCCCTTGAAAGGATCCTGAGAGAGGGGGGAAAGGGAAAACAGCAGCCACCAGCCC CAACATCTAAGCCCTTGAAAGGATCCTGAGAGGGGGGGGAAAGGGAAAACAGCAGCCACCAGCCC T C PPP1R10 Ensembl:ENSG00000204569 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30616857..30616958 26863196 MeRIP-seq:(Medium) rs1021455683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947418,Human_RBP_ID_1670404,Human_RBP_ID_3002800,Human_RBP_ID_15783572,Human_RBP_ID_18862355,Human_RBP_ID_22104807,Human_RBP_ID_23120272,Human_RBP_ID_26353591 Human_Splice_Rec_749058,Human_Splice_Rec_749108,Human_Splice_Rec_749114 75301 RMVar_ID_75301 Human_SNP_ID_271735460 m1A Human chr6 - 30617903 30617903 30617903 TGTGAGAACCTCGGAAGAGAGATAGCATAGGAAGCCGCCTCAGCACGGTGTTTAATACAGACGCC TGTGAGAACCTCGGAAGAGAGATAGCATAGGACGCCGCCTCAGCACGGTGTTTAATACAGACGCC T G PPP1R10 Ensembl:ENSG00000204569 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:30617826..30617968;chr6:30617851..30617972;chr6:30617851..30617982 26863196 MeRIP-seq:(Medium) rs540764576 Functional Loss SNV dbSNP153 33..33 33 - - - 75302 RMVar_ID_75302 Human_SNP_ID_271735465 m1A Human chr6 + 30617908 30617908 30617908 CTGTATTAAACACCGTGCTGAGGCGGCTTCCTATGCTATCTCTCTTCCGAGGTTCTCACAGAGTT CTGTATTAAACACCGTGCTGAGGCGGCTTCCTGTGCTATCTCTCTTCCGAGGTTCTCACAGAGTT A G MRPS18B Ensembl:ENSG00000204568 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:30617851..30617975 26863410 MeRIP-seq:(Medium) rs780014456 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_660831,Human_RBP_ID_1670407,Human_RBP_ID_4879501,Human_RBP_ID_8641637,Human_RBP_ID_18073178 Human_Splice_Rec_749115,Human_Splice_Rec_749127,Human_Splice_Rec_749133,Human_Splice_Rec_749141 RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 75303 RMVar_ID_75303 Human_SNP_ID_271735493 m1A Human chr6 + 30617935 30617935 30617935 TTCCTATGCTATCTCTCTTCCGAGGTTCTCACAGAGTTCAGGTAACTCTTCGAAAGACATTTTGC TTCCTATGCTATCTCTCTTCCGAGGTTCTCACCGAGTTCAGGTAACTCTTCGAAAGACATTTTGC A C MRPS18B Ensembl:ENSG00000204568 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:30617848..30617983 26863196 MeRIP-seq:(Medium) rs569622742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19130363 Human_Splice_Rec_749115,Human_Splice_Rec_749127,Human_Splice_Rec_749133,Human_Splice_Rec_749141 Human_miRNA_ID_2672241 RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 75304 RMVar_ID_75304 Human_SNP_ID_271735494 m1A Human chr6 + 30617935 30617935 30617935 TTCCTATGCTATCTCTCTTCCGAGGTTCTCACAGAGTTCAGGTAACTCTTCGAAAGACATTTTGC TTCCTATGCTATCTCTCTTCCGAGGTTCTCACGGAGTTCAGGTAACTCTTCGAAAGACATTTTGC A G MRPS18B Ensembl:ENSG00000204568 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:30617848..30617983 26863196 MeRIP-seq:(Medium) rs569622742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19130363 Human_Splice_Rec_749115,Human_Splice_Rec_749127,Human_Splice_Rec_749133,Human_Splice_Rec_749141 Human_miRNA_ID_2672241 RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 75305 RMVar_ID_75305 Human_SNP_ID_271736987 m1A Human chr6 + 30622893 30622893 30622893 CGCCCACACGGGTATCATCTTCTATGCTCCATACACAGGTTAGCCCATCATCCCTGCACCACCAG CGCCCACACGGGTATCATCTTCTATGCTCCATTCACAGGTTAGCCCATCATCCCTGCACCACCAG A T MRPS18B Ensembl:ENSG00000204568 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30622876..30622900 32194978 MeRIP-seq:(Medium) rs1363154359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790721,Human_RBP_ID_18073180,Human_RBP_ID_22461790,Human_RBP_ID_22772684 Human_Splice_Rec_749122,Human_Splice_Rec_749123,Human_Splice_Rec_749136,Human_Splice_Rec_749137,Human_Splice_Rec_749148,Human_Splice_Rec_749149 RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 75306 RMVar_ID_75306 Human_SNP_ID_271738181 m1A Human chr6 + 30626952 30626952 30626952 CGGAGCGGATCACGGTGCTGGACCAGCACCTGAGGCCCCCAGCCCGCCGACCCGGAACCACAACG CGGAGCGGATCACGGTGCTGGACCAGCACCTGGGGCCCCCAGCCCGCCGACCCGGAACCACAACG A G ATAT1 Ensembl:ENSG00000137343 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30626908..30627044 26863196 MeRIP-seq:(Medium) rs1289989867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23067780 Human_Splice_Rec_749153,Human_Splice_Rec_749169,Human_Splice_Rec_749217,Human_Splice_Rec_749235,Human_Splice_Rec_749253,Human_Splice_Rec_749273,Human_Splice_Rec_749295,Human_Splice_Rec_749309 75307 RMVar_ID_75307 Human_SNP_ID_271740472 m1A Human chr6 + 30636628 30636628 30636628 AATAAATAAATAAAAATAAACCACCTTTCAGGACACTACAAGCAGTGTGGTGTGGTTGGAGTGCT AATAAATAAATAAAAATAAACCACCTTTCAGGGCACTACAAGCAGTGTGGTGTGGTTGGAGTGCT A G ATAT1 Ensembl:ENSG00000137343 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30636623..30636751 26863196 MeRIP-seq:(Medium) rs11757995 Functional Loss SNV dbSNP153 33..33 33 - - - 75308 RMVar_ID_75308 Human_SNP_ID_271742831 m1A Human chr6 - 30645851 30645851 30645851 ATGGGAGATGATGGGGAGGAGGCTACTGGATGAAAGATGGGTGGGTATGGAGGAATCAGAGGAGA ATGGGAGATGATGGGGAGGAGGCTACTGGATGTAAGATGGGTGGGTATGGAGGAATCAGAGGAGA T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30645830..30645918 26863196 MeRIP-seq:(Medium) rs749551231 Functional Loss SNV dbSNP153 33..33 33 - - - 75309 RMVar_ID_75309 Human_SNP_ID_271743266 m1A Human chr6 - 30647179 30647179 30647179 GGAGCCTCCTGAGTCCGACCTCCGGCCTCCTCACAGGGGTGAGCGCGCCCCAGAGCCGGCTTCGT GGAGCCTCCTGAGTCCGACCTCCGGCCTCCTCGCAGGGGTGAGCGCGCCCCAGAGCCGGCTTCGT T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30647129..30647630 26863196 MeRIP-seq:(Medium) rs1226929581 Functional Loss SNV dbSNP153 33..33 33 - - - 75310 RMVar_ID_75310 Human_SNP_ID_271743270 m1A Human chr6 - 30647194 30647187 30647194 TCCGGGAGTGGAGAAGGAGCCTCCTGAGTCCGACCTCCGGCCTCCTCACAGGGGTGAGCGCGCCC TCCGGGAGTGGAGAAGGAGCCTCCTGAGTCCG_______GCCTCCTCACAGGGGTGAGCGCGCCC CCGGAGGT C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30647150..30647276 26863196 MeRIP-seq:(Medium) rs778501376 Functional Loss DEL dbSNP153 33..39 33 - - - 75311 RMVar_ID_75311 Human_SNP_ID_271743284 m1A Human chr6 - 30647215 30647215 30647215 GGCTGGGCTGGTACATGATCTTCCGGGAGTGGAGAAGGAGCCTCCTGAGTCCGACCTCCGGCCTC GGCTGGGCTGGTACATGATCTTCCGGGAGTGGGGAAGGAGCCTCCTGAGTCCGACCTCCGGCCTC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30647165..30647270 26863196 MeRIP-seq:(Medium) rs1322980887 Functional Loss SNV dbSNP153 33..33 33 - - - 75312 RMVar_ID_75312 Human_SNP_ID_271744022 m1A Human chr6 + 30649612 30649612 30649612 TACCATTCCCACCCCTTTGGCCCCACTCCACGACAACCACTTCCCCATCTTCTCCTCTATTCTGG TACCATTCCCACCCCTTTGGCCCCACTCCACGGCAACCACTTCCCCATCTTCTCCTCTATTCTGG A G C6orf136 Ensembl:ENSG00000204564 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:30649548..30649766;chr6:30647826..30649834 26863196 MeRIP-seq:(Medium) rs117013517 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17421506,Human_RBP_ID_18958078,Human_RBP_ID_27526942 Human_Splice_Rec_749352,Human_Splice_Rec_749362,Human_Splice_Rec_749372,Human_Splice_Rec_749386,Human_Splice_Rec_749406,Human_Splice_Rec_749408 75313 RMVar_ID_75313 Human_SNP_ID_271744033 m1A Human chr6 - 30649645 30649645 30649645 ACGCTGGGTGGGAAGGCGTGGGGGCAGGGGAGACCAGAATAGAGGAGAAGATGGGGAAGTGGTTG ACGCTGGGTGGGAAGGCGTGGGGGCAGGGGAGGCCAGAATAGAGGAGAAGATGGGGAAGTGGTTG T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30649524..30649856 26863196 MeRIP-seq:(Medium) rs752055142 Functional Loss SNV dbSNP153 33..33 33 - - - 75314 RMVar_ID_75314 Human_SNP_ID_271744034 m1A Human chr6 - 30649645 30649645 30649645 ACGCTGGGTGGGAAGGCGTGGGGGCAGGGGAGACCAGAATAGAGGAGAAGATGGGGAAGTGGTTG ACGCTGGGTGGGAAGGCGTGGGGGCAGGGGAGCCCAGAATAGAGGAGAAGATGGGGAAGTGGTTG T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30649524..30649856 26863196 MeRIP-seq:(Medium) rs752055142 Functional Loss SNV dbSNP153 33..33 33 - - - 75315 RMVar_ID_75315 Human_SNP_ID_271744983 m1A Human chr6 + 30652934 30652934 30652934 GTTCCAAGCCCTGATCCTTGACCTTGGAGTGGAGGCAGCACTGAAGACTGCTACGCCCAAGAGAA GTTCCAAGCCCTGATCCTTGACCTTGGAGTGGCGGCAGCACTGAAGACTGCTACGCCCAAGAGAA A C C6orf136 Ensembl:ENSG00000204564 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30652815..30653013 32194978 MeRIP-seq:(Medium) rs753361205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660878,Human_RBP_ID_5121871,Human_RBP_ID_5152067,Human_RBP_ID_18862378,Human_RBP_ID_21902852,Human_RBP_ID_22462562 Human_miRNA_ID_329243,Human_miRNA_ID_333265,Human_miRNA_ID_350313 75316 RMVar_ID_75316 Human_SNP_ID_271746734 m1A Human chr6 + 30659551 30659551 30659551 CAGAGGGCAGATTGGCATAAATGGGCAGCACCAGGAGCTCCCGGATTTTGGAGCCCAGGCGGCGG CAGAGGGCAGATTGGCATAAATGGGCAGCACCGGGAGCTCCCGGATTTTGGAGCCCAGGCGGCGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30659501..30659825 32194978 MeRIP-seq:(Medium) rs776063184 Functional Loss SNV dbSNP153 33..33 33 - - - 75317 RMVar_ID_75317 Human_SNP_ID_271749599 m1A Human chr6 - 30671080 30671080 30671080 AAGCGGAAACACCTCAGGAAGAAGCGTGAGGAAGAAGAGGAGGAAGAGGCTTCTGAGAAAGGGAA AAGCGGAAACACCTCAGGAAGAAGCGTGAGGAGGAAGAGGAGGAAGAGGCTTCTGAGAAAGGGAA T C DHX16 Ensembl:ENSG00000204560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30670801..30671223 26863196 MeRIP-seq:(Medium) rs757267478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3969619,Human_RBP_ID_9400225,Human_RBP_ID_23067782,Human_RBP_ID_23116449,Human_RBP_ID_24548557,Human_RBP_ID_24554606,Human_RBP_ID_26354873 Human_Splice_Rec_749459,Human_Splice_Rec_749501 RMVar_hsa_circ_378786 75318 RMVar_ID_75318 Human_SNP_ID_271749620 m1A Human chr6 - 30671121 30671121 30671121 CTGTGAGTAGGGCTGGAAGCAGCCTCCAGAAGAAACGTAAAAAGCGGAAACACCTCAGGAAGAAG CTGTGAGTAGGGCTGGAAGCAGCCTCCAGAAGGAACGTAAAAAGCGGAAACACCTCAGGAAGAAG T C DHX16 Ensembl:ENSG00000204560 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr6:30670996..30671213;chr6:30670876..30671275 26863196 MeRIP-seq:(Medium) rs776246488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18073223,Human_RBP_ID_23116449,Human_RBP_ID_24548557,Human_RBP_ID_26354874 Human_Splice_Rec_749459,Human_Splice_Rec_749501 RMVar_hsa_circ_378786 75319 RMVar_ID_75319 Human_SNP_ID_271750164 m1A Human chr6 + 30672950 30672950 30672950 AGCCCTCGGCTGGAGCCTCAGCTTCGCAAGTCAGCTACCTTGGGACCTCTAGGATCTTCCGACAT AGCCCTCGGCTGGAGCCTCAGCTTCGCAAGTCCGCTACCTTGGGACCTCTAGGATCTTCCGACAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30672787..30673000 26863196 MeRIP-seq:(Medium) rs981492087 Functional Loss SNV dbSNP153 33..33 33 - - - 75320 RMVar_ID_75320 Human_SNP_ID_271750177 m1A Human chr6 - 30672965 30672965 30672965 GAAGACAGCTTTGGGATGTCGGAAGATCCTAGAGGTCCCAAGGTAGCTGACTTGCGAAGCTGAGG GAAGACAGCTTTGGGATGTCGGAAGATCCTAGCGGTCCCAAGGTAGCTGACTTGCGAAGCTGAGG T G DHX16 Ensembl:ENSG00000204560 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr6:30672722..30673025;chr6:30672776..30673000 26863196 MeRIP-seq:(Medium) rs960053284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4879679,Human_RBP_ID_18425387 Human_Splice_Rec_749499 75321 RMVar_ID_75321 Human_SNP_ID_271751111 m1A Human chr6 + 30676807 30676807 30676807 TAAACCAGGCTGTGGTCAAGGGAGGAGGCAGGAGCTGTAAACAAAGGGGCAGTGACCTAGGAAAT TAAACCAGGCTGTGGTCAAGGGAGGAGGCAGGGGCTGTAAACAAAGGGGCAGTGACCTAGGAAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30676757..30676843 26863196 MeRIP-seq:(Medium) rs954856603 Functional Loss SNV dbSNP153 33..33 33 - - - 75322 RMVar_ID_75322 Human_SNP_ID_271752056 m1A Human chr6 - 30681167 30681160 30681168 GGAAGAGGCCAGAGAGGCAAGGGGAGGGTGGCATACTGGGAGCACCCTGTAGGCTTTGGTCAGGC GGAAGAGGCCAGAGAGGCAAGGGGAGGGTGG________GAGCACCCTGTAGGCTTTGGTCAGGC CCCAGTATG C PPP1R18 Ensembl:ENSG00000146112 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30681165..30681367 26863196 MeRIP-seq:(Medium) rs1476384667 Functional Loss DEL dbSNP153 32..39 33 - - - 75323 RMVar_ID_75323 Human_SNP_ID_271752063 m1A Human chr6 + 30681233 30681233 30681233 CCACTCCAGCCACACTGGCCTTGGTTCCCTCCACGCACTCCTACCTCAGGACCAGAACAGTACTA CCACTCCAGCCACACTGGCCTTGGTTCCCTCCGCGCACTCCTACCTCAGGACCAGAACAGTACTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30681221..30681355 26863196 MeRIP-seq:(Medium) rs904446773 Functional Loss SNV dbSNP153 33..33 33 - - - 75324 RMVar_ID_75324 Human_SNP_ID_271753591 m1A Human chr6 + 30687161 30687160 30687162 CGGGGGAGGGGGTGCGGAGGAGCCGGGCGTCCAGAGAGAGGAAGAGGAGGAGAGAGGGACCGAGG CGGGGGAGGGGGTGCGGAGGAGCCGGGCGTCC__AGAGAGGAAGAGGAGGAGAGAGGGACCGAGG CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30686794..30687189 26863196 MeRIP-seq:(Medium) rs1435686422 Functional Loss DEL dbSNP153 33..34 33 - - - 75325 RMVar_ID_75325 Human_SNP_ID_271753841 m1A Human chr6 - 30688265 30688265 30688265 CACCGCTGGCTTCCACTCCAAGAAGGTGGACCAGGGTCTGCAAGTTCAACGGTCATAGCTGTCCC CACCGCTGGCTTCCACTCCAAGAAGGTGGACCGGGGTCTGCAAGTTCAACGGTCATAGCTGTCCC T C NRM Ensembl:ENSG00000137404 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30688146..30688425 32194978 MeRIP-seq:(Medium) rs11539190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660909,Human_RBP_ID_17306339,Human_RBP_ID_18862410,Human_RBP_ID_18958087 75326 RMVar_ID_75326 Human_SNP_ID_271754587 m1A Human chr6 + 30690933 30690933 30690933 AACTCCACTCCGGTGCCAAAGGCCAGGATGAAAGAGGCGAGGGCAGCAGGGATCAGGAGCAGTGC AACTCCACTCCGGTGCCAAAGGCCAGGATGAATGAGGCGAGGGCAGCAGGGATCAGGAGCAGTGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30690826..30690975 26863196 MeRIP-seq:(Medium) rs761830153 Functional Loss SNV dbSNP153 33..33 33 - - - 75327 RMVar_ID_75327 Human_SNP_ID_271754596 m1A Human chr6 + 30690958 30690958 30690958 GGATGAAAGAGGCGAGGGCAGCAGGGATCAGGAGCAGTGCAGGGGCCATGGCGAGAAATGGAGGG GGATGAAAGAGGCGAGGGCAGCAGGGATCAGGCGCAGTGCAGGGGCCATGGCGAGAAATGGAGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30690332..30691000 26863196 MeRIP-seq:(Medium) rs778744718 Functional Loss SNV dbSNP153 33..33 33 - - - 75328 RMVar_ID_75328 Human_SNP_ID_271757650 m1A Human chr6 - 30703472 30703472 30703472 AGAGACCAGGCAGAGGAGGAGCCCAACAGAATACCAAGCCGCAGCCTCCGACGGACCAAACTTAA AGAGACCAGGCAGAGGAGGAGCCCAACAGAATCCCAAGCCGCAGCCTCCGACGGACCAAACTTAA T G MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30703421..30703725 26863196 MeRIP-seq:(Medium) rs2239885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252267,Human_RBP_ID_4879819,Human_RBP_ID_9400229,Human_RBP_ID_21322730,Human_RBP_ID_23059856,Human_RBP_ID_26353609 Human_Splice_Rec_749598,Human_Splice_Rec_749599,Human_Splice_Rec_749607 75329 RMVar_ID_75329 Human_SNP_ID_271757815 m1A Human chr6 - 30703964 30703964 30703964 CCCTGGCTCCCTCGCAGCTCCCATTGACCATAAGCCTTGCTCTGCACCCTTGGAACCTAAATCCC CCCTGGCTCCCTCGCAGCTCCCATTGACCATAGGCCTTGCTCTGCACCCTTGGAACCTAAATCCC T C MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30703913..30704014 32194978 MeRIP-seq:(Medium) rs1371679526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660963,Human_RBP_ID_1670465,Human_RBP_ID_3805884,Human_RBP_ID_4879831,Human_RBP_ID_7591494,Human_RBP_ID_8899781,Human_RBP_ID_15783969,Human_RBP_ID_17306361,Human_RBP_ID_17419527,Human_RBP_ID_18862431 75330 RMVar_ID_75330 Human_SNP_ID_271757928 m1A Human chr6 + 30704285 30704285 30704285 TATTTGTCTTTCTCCTAGTGGCCCTAGATGTGAGCTTGGGGGTGACAGGCTGGTCTGTGGAGGTG TATTTGTCTTTCTCCTAGTGGCCCTAGATGTGGGCTTGGGGGTGACAGGCTGGTCTGTGGAGGTG A G MDC1-AS1 Ensembl:ENSG00000224328 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30704236..30704649 26863196 MeRIP-seq:(Medium) rs867695298 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 75331 RMVar_ID_75331 Human_SNP_ID_271758074 m1A Human chr6 + 30704573 30704573 30704573 TGACAGGTTGGTCTGTGGAGGTGGAAGGCTGGAGCTCAGGGGCTGCGGGCACAACTGTTTCAGGG TGACAGGTTGGTCTGTGGAGGTGGAAGGCTGGGGCTCAGGGGCTGCGGGCACAACTGTTTCAGGG A G MDC1-AS1 Ensembl:ENSG00000224328 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:30704526..30704650 26863196 MeRIP-seq:(Medium) rs1348676176 Functional Loss SNV dbSNP153 33..33 33 - - - 75332 RMVar_ID_75332 Human_SNP_ID_271758289 m1A Human chr6 - 30705001 30705001 30705001 ACCCCTGAGCCCACATCTCGGGCTACTAGGGGAAGAAAAAATAGATCCTCTGGCAAGACCCCTGA ACCCCTGAGCCCACATCTCGGGCTACTAGGGGCAGAAAAAATAGATCCTCTGGCAAGACCCCTGA T G MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30704951..30705326 26863196 MeRIP-seq:(Medium) rs1444337515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2018170,Human_RBP_ID_3805888,Human_RBP_ID_8899789,Human_RBP_ID_17421527,Human_RBP_ID_23059862,Human_RBP_ID_26046029 75333 RMVar_ID_75333 Human_SNP_ID_271758329 m1A Human chr6 + 30705090 30705090 30705090 AGGTGGGAGCTCAGGGGCTATAGGGACAGTTGATTCAGGGTTCTTCACAGAGGACATATTTGTCC AGGTGGGAGCTCAGGGGCTATAGGGACAGTTGGTTCAGGGTTCTTCACAGAGGACATATTTGTCC A G MDC1-AS1 Ensembl:ENSG00000224328 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30704876..30705300 26863196 MeRIP-seq:(Medium) rs1277124877 Functional Loss SNV dbSNP153 33..33 33 - - - 75334 RMVar_ID_75334 Human_SNP_ID_271758536 m1A Human chr6 - 30705501 30705501 30705501 GACCTGTCACCTCTGAACCCACCTCTCAGGCTACTAGGGGAAGAAAAAATAGATCCTCTGTCAAG GACCTGTCACCTCTGAACCCACCTCTCAGGCTTCTAGGGGAAGAAAAAATAGATCCTCTGTCAAG T A MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30705453..30705633 26863196 MeRIP-seq:(Medium) rs759720887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4879844,Human_RBP_ID_15784030,Human_RBP_ID_17306377,Human_RBP_ID_23068848,Human_RBP_ID_27522929 75335 RMVar_ID_75335 Human_SNP_ID_271759273 m1A Human chr6 - 30707816 30707816 30707816 CCAAGCAAAGCATTTGAGAGAGAAGTAGAGAGACCAGTAGCAAACAGAGAGTGCGATCCAGCCGA CCAAGCAAAGCATTTGAGAGAGAAGTAGAGAGGCCAGTAGCAAACAGAGAGTGCGATCCAGCCGA T C MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30707701..30707875 26863196 MeRIP-seq:(Medium) rs776981504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046664,Human_RBP_ID_7591509,Human_RBP_ID_8899797,Human_RBP_ID_15784096 75336 RMVar_ID_75336 Human_SNP_ID_271760223 m1A Human chr6 + 30711970 30711970 30711970 GACCTGGGCTCCCTCTCTCTGTGGCTGGGTGGATTCCCCTAGAGTGTCTGTGTCCACCACCAGAT GACCTGGGCTCCCTCTCTCTGTGGCTGGGTGGGTTCCCCTAGAGTGTCTGTGTCCACCACCAGAT A G MDC1-AS1 Ensembl:ENSG00000224328 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30711926..30712000 26863196 MeRIP-seq:(Medium) rs528811156 Functional Loss SNV dbSNP153 33..33 33 - - - 75337 RMVar_ID_75337 Human_SNP_ID_271760572 m1A Human chr6 - 30713108 30713108 30713108 AGGGACAATGATACAAAAGTCAAGAGGGGTGCAGGGAATGGGGTGGTTCCAGCTGGGGTGATTCT AGGGACAATGATACAAAAGTCAAGAGGGGTGCGGGGAATGGGGTGGTTCCAGCTGGGGTGATTCT T C MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30713057..30713181 26863196 MeRIP-seq:(Medium) rs750258735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046680,Human_RBP_ID_3968645,Human_RBP_ID_5400304,Human_RBP_ID_5532344,Human_RBP_ID_7591542,Human_RBP_ID_8899849,Human_RBP_ID_9309144,Human_RBP_ID_18073284,Human_RBP_ID_18413837,Human_RBP_ID_22727841,Human_RBP_ID_23116450,Human_RBP_ID_26353614,Human_RBP_ID_26771903,Human_RBP_ID_27828397 RMVar_hsa_circ_66652,RMVar_hsa_circ_268062 75338 RMVar_ID_75338 Human_SNP_ID_271761462 m1A Human chr6 + 30716995 30716995 30716995 TTTATGACAGGCCAACTCAGCGGGTGCCCACCACGCTTGGCTCCAATTCAAAGAGCCACCATCTT TTTATGACAGGCCAACTCAGCGGGTGCCCACCGCGCTTGGCTCCAATTCAAAGAGCCACCATCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30716977..30717050 26863196 MeRIP-seq:(Medium) rs376900963 Functional Loss SNV dbSNP153 33..33 33 - - - 75339 RMVar_ID_75339 Human_SNP_ID_271762322 m1A Human chr6 + 30720414 30720414 30720414 ACCTCGCTGCTCCAGCCTCTGGGGCGCATTCCAACCTTCCAGCCTGCGACCTGCGGAGAAAAAAA ACCTCGCTGCTCCAGCCTCTGGGGCGCATTCCTACCTTCCAGCCTGCGACCTGCGGAGAAAAAAA A T TUBB Ensembl:ENSG00000196230 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30720326..30720500 26863196 MeRIP-seq:(Medium) rs1049062641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252427,Human_RBP_ID_284983,Human_RBP_ID_660994,Human_RBP_ID_791174,Human_RBP_ID_1046690,Human_RBP_ID_1670508,Human_RBP_ID_2018212,Human_RBP_ID_3805910,Human_RBP_ID_4880011,Human_RBP_ID_5428385,Human_RBP_ID_5451069,Human_RBP_ID_5478838,Human_RBP_ID_5511377,Human_RBP_ID_7591572,Human_RBP_ID_8641736,Human_RBP_ID_8899874,Human_RBP_ID_9193412,Human_RBP_ID_10279803,Human_RBP_ID_17306387,Human_RBP_ID_17419542,Human_RBP_ID_17537837,Human_RBP_ID_18073296,Human_RBP_ID_18184004,Human_RBP_ID_18195366,Human_RBP_ID_18210995,Human_RBP_ID_18862465,Human_RBP_ID_21322842,Human_RBP_ID_22310752,Human_RBP_ID_22460553,Human_RBP_ID_22831026,Human_RBP_ID_23059888,Human_RBP_ID_24512125,Human_RBP_ID_25995721,Human_RBP_ID_26541027,Human_RBP_ID_26828141,Human_RBP_ID_27095539,Human_RBP_ID_27522967 75340 RMVar_ID_75340 Human_SNP_ID_271762323 m1A Human chr6 + 30720415 30720415 30720415 CCTCGCTGCTCCAGCCTCTGGGGCGCATTCCAACCTTCCAGCCTGCGACCTGCGGAGAAAAAAAA CCTCGCTGCTCCAGCCTCTGGGGCGCATTCCAGCCTTCCAGCCTGCGACCTGCGGAGAAAAAAAA A G TUBB Ensembl:ENSG00000196230 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:30720301..30720588;chr6:30720305..30720559;chr6:30720310..30720588;chr6:30720326..30720515 26863196 MeRIP-seq:(Medium) rs528416403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252427,Human_RBP_ID_284983,Human_RBP_ID_660994,Human_RBP_ID_791174,Human_RBP_ID_1046690,Human_RBP_ID_1670508,Human_RBP_ID_2018212,Human_RBP_ID_3805910,Human_RBP_ID_4880011,Human_RBP_ID_5428385,Human_RBP_ID_5451069,Human_RBP_ID_5478838,Human_RBP_ID_5511377,Human_RBP_ID_7591572,Human_RBP_ID_8641736,Human_RBP_ID_8899874,Human_RBP_ID_9193412,Human_RBP_ID_10279803,Human_RBP_ID_17306387,Human_RBP_ID_17419542,Human_RBP_ID_17537837,Human_RBP_ID_18073296,Human_RBP_ID_18184004,Human_RBP_ID_18195366,Human_RBP_ID_18210995,Human_RBP_ID_18862465,Human_RBP_ID_21322842,Human_RBP_ID_22310752,Human_RBP_ID_22461798,Human_RBP_ID_22831026,Human_RBP_ID_23059888,Human_RBP_ID_24512125,Human_RBP_ID_25995721,Human_RBP_ID_26541027,Human_RBP_ID_26828141,Human_RBP_ID_27095539,Human_RBP_ID_27522967 75341 RMVar_ID_75341 Human_SNP_ID_271763330 m1A Human chr6 + 30723491 30723491 30723491 TTCCAGCTGACCCACTCACTGGGCGGGGGCACAGGCTCTGGAATGGGCACTCTCCTTATCAGCAA TTCCAGCTGACCCACTCACTGGGCGGGGGCACGGGCTCTGGAATGGGCACTCTCCTTATCAGCAA A G TUBB Ensembl:ENSG00000196230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30723441..30723506 26863196 MeRIP-seq:(Medium) rs761579092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661004,Human_RBP_ID_1046698,Human_RBP_ID_1670522,Human_RBP_ID_2018225,Human_RBP_ID_7591598,Human_RBP_ID_8270085,Human_RBP_ID_8641750,Human_RBP_ID_8899882,Human_RBP_ID_9193417,Human_RBP_ID_15784250,Human_RBP_ID_17306396,Human_RBP_ID_17419548,Human_RBP_ID_18073307,Human_RBP_ID_18195370,Human_RBP_ID_18450096,Human_RBP_ID_22460559,Human_RBP_ID_22513960,Human_RBP_ID_22534065,Human_RBP_ID_22616083,Human_RBP_ID_22773368,Human_RBP_ID_23138818,Human_RBP_ID_24156505,Human_RBP_ID_26829309,Human_RBP_ID_27161074 75342 RMVar_ID_75342 Human_SNP_ID_271763438 m1A Human chr6 + 30724176 30724176 30724176 TCAAGATGGCAGTCACCTTCATTGGCAATAGCACAGCCATCCAGGAGCTCTTCAAGCGCATCTCG TCAAGATGGCAGTCACCTTCATTGGCAATAGCTCAGCCATCCAGGAGCTCTTCAAGCGCATCTCG A T TUBB Ensembl:ENSG00000196230 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30723426..30724175 32194978 MeRIP-seq:(Medium) rs2394395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661028,Human_RBP_ID_1046709,Human_RBP_ID_1217113,Human_RBP_ID_1670539,Human_RBP_ID_2018237,Human_RBP_ID_3002887,Human_RBP_ID_3805928,Human_RBP_ID_4880049,Human_RBP_ID_7591622,Human_RBP_ID_8270088,Human_RBP_ID_8641767,Human_RBP_ID_17306411,Human_RBP_ID_17419559,Human_RBP_ID_17535528,Human_RBP_ID_18073318,Human_RBP_ID_18370092,Human_RBP_ID_18862488,Human_RBP_ID_21393239,Human_RBP_ID_22310793,Human_RBP_ID_22460567,Human_RBP_ID_22773372,Human_RBP_ID_22831043,Human_RBP_ID_26535198,Human_RBP_ID_27095582,Human_RBP_ID_27345235,Human_RBP_ID_27523006 75343 RMVar_ID_75343 Human_SNP_ID_271763489 m1A Human chr6 + 30724385 30724373 30724385 GAAGAGGAGGAGGATTTCGGTGAGGAGGCCGAAGAGGAGGCCTAAGGCAGAGCCCCCATCACCTC GAAGAGGAGGAGGATTTCGGT____________GAGGAGGCCTAAGGCAGAGCCCCCATCACCTC TGAGGAGGCCGAA T TUBB Ensembl:ENSG00000196230 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:30724282..30724424 26863196 MeRIP-seq:(Medium) rs747584215 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_252436,Human_RBP_ID_661032,Human_RBP_ID_791183,Human_RBP_ID_1046710,Human_RBP_ID_1326824,Human_RBP_ID_2018243,Human_RBP_ID_3805931,Human_RBP_ID_7591631,Human_RBP_ID_15784290,Human_RBP_ID_17306413,Human_RBP_ID_17663925,Human_RBP_ID_18073319,Human_RBP_ID_18195381,Human_RBP_ID_22106717,Human_RBP_ID_22460568,Human_RBP_ID_23138822,Human_RBP_ID_24156515 75344 RMVar_ID_75344 Human_SNP_ID_271763504 m1A Human chr6 + 30724410 30724410 30724410 AGGCCGAAGAGGAGGCCTAAGGCAGAGCCCCCATCACCTCAGGCTTCTCAGTTCCCTTAGCCGTC AGGCCGAAGAGGAGGCCTAAGGCAGAGCCCCCGTCACCTCAGGCTTCTCAGTTCCCTTAGCCGTC A G TUBB Ensembl:ENSG00000196230 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30724359..30724488 26863196 MeRIP-seq:(Medium) rs1382769679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21221609 75345 RMVar_ID_75345 Human_SNP_ID_271763696 m1A Human chr6 - 30725049 30725038 30725050 AACCCCCTTGATCCCTTTCTCTGATCAGGGGAAAGGAGCTGAGTGAGGGAGGTAGAGTTGGAAAG AACCCCCTTGATCCCTTTCTCTGATCAGGGG____________TGAGGGAGGTAGAGTTGGAAAG ACTCAGCTCCTTT A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30725001..30725150 26863196 MeRIP-seq:(Medium) rs1371001209 Functional Loss DEL dbSNP153 32..43 33 - - - 75346 RMVar_ID_75346 Human_SNP_ID_271763696 m1A Human chr6 - 30725050 30725038 30725050 CAACCCCCTTGATCCCTTTCTCTGATCAGGGGAAAGGAGCTGAGTGAGGGAGGTAGAGTTGGAAA CAACCCCCTTGATCCCTTTCTCTGATCAGGGG____________TGAGGGAGGTAGAGTTGGAAA ACTCAGCTCCTTT A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30725001..30725400 32194978 MeRIP-seq:(Medium) rs1371001209 Functional Loss DEL dbSNP153 33..44 33 - - - 75347 RMVar_ID_75347 Human_SNP_ID_271763776 m1A Human chr6 + 30725250 30725250 30725250 TCAGTCCCCAGAGGAGAGGGGAACCCTCCTCCATCTTTTTTGCAACATCTCATTTCTTCCTTTTG TCAGTCCCCAGAGGAGAGGGGAACCCTCCTCCGTCTTTTTTGCAACATCTCATTTCTTCCTTTTG A G TUBB Ensembl:ENSG00000196230 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30725176..30725300 26863196 MeRIP-seq:(Medium) rs1400674180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661067,Human_RBP_ID_3002928,Human_RBP_ID_3805943,Human_RBP_ID_7591672,Human_RBP_ID_15936230,Human_RBP_ID_17537851,Human_RBP_ID_18862499,Human_RBP_ID_21322924,Human_RBP_ID_22102907,Human_RBP_ID_22831059,Human_RBP_ID_24435601,Human_RBP_ID_24512160,Human_RBP_ID_26535228,Human_RBP_ID_27095601,Human_RBP_ID_27345252 Human_miRNA_ID_303087,Human_miRNA_ID_1382615 75348 RMVar_ID_75348 Human_SNP_ID_271764972 m1A Human chr6 - 30730117 30730117 30730117 ATAAGATCACACTGGTGTCCAGCGGCAGTGGGACCATGGGGGCAGCCAAAGTGACTGGGGAAGTA ATAAGATCACACTGGTGTCCAGCGGCAGTGGGCCCATGGGGGCAGCCAAAGTGACTGGGGAAGTA T G FLOT1 Ensembl:ENSG00000137312 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30730067..30730210 26863196 MeRIP-seq:(Medium) rs1158438188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661090,Human_RBP_ID_5122353,Human_RBP_ID_5151804,Human_RBP_ID_5532346,Human_RBP_ID_18073344,Human_RBP_ID_18195383,Human_RBP_ID_22461812,Human_RBP_ID_26829329 Human_Splice_Rec_749688,Human_Splice_Rec_749689,Human_Splice_Rec_749712,Human_Splice_Rec_749713 Human_miRNA_ID_2150927,Human_miRNA_ID_2419415 RMVar_hsa_circ_237818,RMVar_hsa_circ_377736 75349 RMVar_ID_75349 Human_SNP_ID_271765098 m1A Human chr6 - 30730536 30730536 30730536 CAGATGCGTGGGGAAGCTGAGGCCTTTGCCATAGGGGCCCGAGCCCGAGCCGAGGCTGAGCAGAT CAGATGCGTGGGGAAGCTGAGGCCTTTGCCATGGGGGCCCGAGCCCGAGCCGAGGCTGAGCAGAT T C FLOT1 Ensembl:ENSG00000137312 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30730426..30730575 32194978 MeRIP-seq:(Medium) rs961682492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949186,Human_RBP_ID_3968647,Human_RBP_ID_4880109,Human_RBP_ID_5399329,Human_RBP_ID_19016533,Human_RBP_ID_22460569 Human_Splice_Rec_749686,Human_Splice_Rec_749710 Human_miRNA_ID_2295130,Human_miRNA_ID_2579598 RMVar_hsa_circ_237818,RMVar_hsa_circ_377736 75350 RMVar_ID_75350 Human_SNP_ID_271765100 m1A Human chr6 - 30730538 30730538 30730538 CTCAGATGCGTGGGGAAGCTGAGGCCTTTGCCATAGGGGCCCGAGCCCGAGCCGAGGCTGAGCAG CTCAGATGCGTGGGGAAGCTGAGGCCTTTGCCGTAGGGGCCCGAGCCCGAGCCGAGGCTGAGCAG T C FLOT1 Ensembl:ENSG00000137312 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30730451..30730575 32194978 MeRIP-seq:(Medium) rs199886114 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_661093,Human_RBP_ID_949186,Human_RBP_ID_3968647,Human_RBP_ID_5399329,Human_RBP_ID_19016533,Human_RBP_ID_22460569 Human_Splice_Rec_749686,Human_Splice_Rec_749710 Human_miRNA_ID_2295130,Human_miRNA_ID_2579598 RMVar_hsa_circ_237818,RMVar_hsa_circ_377736 75351 RMVar_ID_75351 Human_SNP_ID_271765154 m1A Human chr6 + 30730713 30730713 30730713 CCCGCACAGACGCGGCTTCTGCCTCCGCCTGCATAATTAGTTGGGACCTGTGGACAGAAGGGAAG CCCGCACAGACGCGGCTTCTGCCTCCGCCTGCTTAATTAGTTGGGACCTGTGGACAGAAGGGAAG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30730676..30730750 32194978 MeRIP-seq:(Medium) rs750909604 Functional Loss SNV dbSNP153 33..33 33 - - - 75352 RMVar_ID_75352 Human_SNP_ID_271765159 m1A Human chr6 + 30730726 30730726 30730726 GGCTTCTGCCTCCGCCTGCATAATTAGTTGGGACCTGTGGACAGAAGGGAAGTGGAGGGTGGAGC GGCTTCTGCCTCCGCCTGCATAATTAGTTGGGTCCTGTGGACAGAAGGGAAGTGGAGGGTGGAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:30730651..30730770;chr6:30730701..30730750 26863196 MeRIP-seq:(Medium) rs958858574 Functional Loss SNV dbSNP153 33..33 33 - - - 75353 RMVar_ID_75353 Human_SNP_ID_271765161 m1A Human chr6 - 30730729 30730729 30730729 TGGGCTCCACCCTCCACTTCCCTTCTGTCCACAGGTCCCAACTAATTATGCAGGCGGAGGCAGAA TGGGCTCCACCCTCCACTTCCCTTCTGTCCACGGGTCCCAACTAATTATGCAGGCGGAGGCAGAA T C FLOT1 Ensembl:ENSG00000137312 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30730726..30730750 26863196 MeRIP-seq:(Medium) rs1411201844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949188,Human_RBP_ID_3968648,Human_RBP_ID_19130406,Human_RBP_ID_22553576,Human_RBP_ID_22684650,Human_RBP_ID_26040039 Human_Splice_Rec_749685,Human_Splice_Rec_749709 RMVar_hsa_circ_237818,RMVar_hsa_circ_377736 75354 RMVar_ID_75354 Human_SNP_ID_271765249 m1A Human chr6 + 30731048 30731048 30731048 GCTCCTGCACTGCCACCTGCTGGGCCCGCTCCACCACCTGCACCTGCACCCGCTGCTCCTCAATC GCTCCTGCACTGCCACCTGCTGGGCCCGCTCCCCCACCTGCACCTGCACCCGCTGCTCCTCAATC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:30731001..30731050 26863196 MeRIP-seq:(Medium) rs1453673619 Functional Loss SNV dbSNP153 33..33 33 - - - 75355 RMVar_ID_75355 Human_SNP_ID_271766593 m1A Human chr6 + 30736942 30736942 30736942 CCGTTCTCCACAAGGCAACCAGACTGATCCCTATACAAATATAAATAAGACCATGGCACCTTTCT CCGTTCTCCACAAGGCAACCAGACTGATCCCTGTACAAATATAAATAAGACCATGGCACCTTTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30736937..30737226 26863196 MeRIP-seq:(Medium) rs1459556337 Functional Loss SNV dbSNP153 33..33 33 - - - 75356 RMVar_ID_75356 Human_SNP_ID_271766605 m1A Human chr6 - 30737016 30737016 30737016 GGGTTTGTGTGGTCACGATGGAGACACAGAAGAGAACTGAAAGCACAGTGGAAAGCTATTGGAGA GGGTTTGTGTGGTCACGATGGAGACACAGAAGTGAACTGAAAGCACAGTGGAAAGCTATTGGAGA T A FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30737013..30737167 26863196 MeRIP-seq:(Medium) rs140232828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17198398,Human_RBP_ID_23059921 75357 RMVar_ID_75357 Human_SNP_ID_271767398 m1A Human chr6 + 30740114 30740114 30740114 GTGTAGTGGTGTCCTGAGATGGACAGCCTGAGAGGAATGGGGAAGGGGCAGAGAGTGGCCTGGCA GTGTAGTGGTGTCCTGAGATGGACAGCCTGAGGGGAATGGGGAAGGGGCAGAGAGTGGCCTGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30740112..30740337 26863196 MeRIP-seq:(Medium) rs747591062 Functional Loss SNV dbSNP153 33..33 33 - - - 75358 RMVar_ID_75358 Human_SNP_ID_271767589 m1A Human chr6 + 30740790 30740790 30740790 AAAACCTGTTCTGAGAATTTCTGCCTGTCCTTATAGATCTCCTGTGATAACAGGATGGTGGGGAG AAAACCTGTTCTGAGAATTTCTGCCTGTCCTTCTAGATCTCCTGTGATAACAGGATGGTGGGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30740656..30740818 26863196 MeRIP-seq:(Medium) rs1222269626 Functional Loss SNV dbSNP153 33..33 33 - - - 75359 RMVar_ID_75359 Human_SNP_ID_271767799 m1A Human chr6 - 30741570 30741570 30741570 AGAGCCTTTTCCCCACAGTCCACTTCCCCATCACCCTCTCTCCCAGACATTAAGACATCTTCTGG AGAGCCTTTTCCCCACAGTCCACTTCCCCATCCCCCTCTCTCCCAGACATTAAGACATCTTCTGG T G FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30741567..30741656 26863196 MeRIP-seq:(Medium) rs1453044366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17090814,Human_RBP_ID_18957178,Human_RBP_ID_19128798 75360 RMVar_ID_75360 Human_SNP_ID_271767903 m1A Human chr6 + 30741843 30741843 30741843 AGGGCAGGACAAAGACACGCCCTCCAGCCACCATGACTGGGGGGCTTCGGCAGAACCCTGCAAGG AGGGCAGGACAAAGACACGCCCTCCAGCCACCCTGACTGGGGGGCTTCGGCAGAACCCTGCAAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30741776..30741875 32194978 MeRIP-seq:(Medium) rs780293211 Functional Loss SNV dbSNP153 33..33 33 - - - 75361 RMVar_ID_75361 Human_SNP_ID_271767904 m1A Human chr6 + 30741843 30741843 30741843 AGGGCAGGACAAAGACACGCCCTCCAGCCACCATGACTGGGGGGCTTCGGCAGAACCCTGCAAGG AGGGCAGGACAAAGACACGCCCTCCAGCCACCGTGACTGGGGGGCTTCGGCAGAACCCTGCAAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30741776..30741875 32194978 MeRIP-seq:(Medium) rs780293211 Functional Loss SNV dbSNP153 33..33 33 - - - 75362 RMVar_ID_75362 Human_SNP_ID_271768132 m1A Human chr6 + 30742593 30742593 30742593 TCGGGAAGGGCGGGGTCGCGCAGGGACCTGGGAGCCGGGCAGGGGCCGCTCGCAGACCAGCTTTC TCGGGAAGGGCGGGGTCGCGCAGGGACCTGGGGGCCGGGCAGGGGCCGCTCGCAGACCAGCTTTC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:30742583..30742683 26863410 MeRIP-seq:(Medium) rs1220074555 Functional Loss SNV dbSNP153 33..33 33 - - - 75363 RMVar_ID_75363 Human_SNP_ID_271768386 m1A Human chr6 + 30743515 30743515 30743515 CCCCATTTCTTCTCCTACTTTGCCGCAGTTCCAGGTGTCCTGCTTCCACCAGTCCCACAAAGCTC CCCCATTTCTTCTCCTACTTTGCCGCAGTTCCGGGTGTCCTGCTTCCACCAGTCCCACAAAGCTC A G IER3-AS1 Ensembl:ENSG00000272273 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30743264..30743555 26863196 MeRIP-seq:(Medium) rs539855130 Functional Loss SNV dbSNP153 33..33 33 - - - 75364 RMVar_ID_75364 Human_SNP_ID_271768433 m1A Human chr6 - 30743769 30743754 30743770 CACCCGGTGCTTGAGGCGGGACCGAGGCGCACAGAGACCGAGGCGCATAGAGACCGAGGCACAGC CACCCGGTGCTTGAGGCGGGACCGAGGCGCA________________TAGAGACCGAGGCACAGC ATGCGCCTCGGTCTCTG A IER3 Ensembl:ENSG00000137331 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30743718..30743850 26863196 MeRIP-seq:(Medium) rs1424846488 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_17537855,Human_RBP_ID_22104821,Human_RBP_ID_27523057 75365 RMVar_ID_75365 Human_SNP_ID_271768436 m1A Human chr6 - 30743769 30743769 30743769 CACCCGGTGCTTGAGGCGGGACCGAGGCGCACAGAGACCGAGGCGCATAGAGACCGAGGCACAGC CACCCGGTGCTTGAGGCGGGACCGAGGCGCACGGAGACCGAGGCGCATAGAGACCGAGGCACAGC T C IER3 Ensembl:ENSG00000137331 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30743718..30743850 26863196 MeRIP-seq:(Medium) rs530162948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17537855,Human_RBP_ID_22104821,Human_RBP_ID_27523057 75366 RMVar_ID_75366 Human_SNP_ID_271768456 m1A Human chr6 - 30743887 30743887 30743887 TCCCCAAAAAGAATCCGAAAAACCACAAAGAAACACCAGGCGTACCTGGTGCGCGAGAGCGTATC TCCCCAAAAAGAATCCGAAAAACCACAAAGAAGCACCAGGCGTACCTGGTGCGCGAGAGCGTATC T C IER3 Ensembl:ENSG00000137331 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30743746..30744124 26863196 MeRIP-seq:(Medium) rs372116534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17308786,Human_RBP_ID_23059934 75367 RMVar_ID_75367 Human_SNP_ID_271768545 m1A Human chr6 + 30744104 30744104 30744104 TCTGGAGGCAGGGGCGCCGGCACACCCTCTTCAGCCATCAGGATCTGGCAGAAGACGATGGTGAG TCTGGAGGCAGGGGCGCCGGCACACCCTCTTCGGCCATCAGGATCTGGCAGAAGACGATGGTGAG A G HCG20 Ensembl:ENSG00000228022 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30744026..30744125 32194978 MeRIP-seq:(Medium) rs150315262 Functional Loss SNV dbSNP153 33..33 33 - - - 75368 RMVar_ID_75368 Human_SNP_ID_271800190 m1A Human chr6 - 30884617 30884610 30884617 CGGGGCGAGGGGCGGGGGAGGCGGAGGGAGCCAGGAGCCGGGAGCCGGGAGCGGGAGGCGCCGGC CGGGGCGAGGGGCGGGGGAGGCGGAGGGAGCC_______GGGAGCCGGGAGCGGGAGGCGCCGGC CGGCTCCT C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:30884601..30884725 26863196 MeRIP-seq:(Medium) rs1171981191 Functional Loss DEL dbSNP153 33..39 33 - - - 75369 RMVar_ID_75369 Human_SNP_ID_271802041 m1A Human chr6 + 30892064 30892064 30892064 AGATGGTGTGGTGGGGCTGGATGACTTTAGGAAGAGTCAGGAGCTGCGGGTCTGGCCAGGCTATG AGATGGTGTGGTGGGGCTGGATGACTTTAGGATGAGTCAGGAGCTGCGGGTCTGGCCAGGCTATG A T DDR1 Ensembl:ENSG00000204580 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:30891980..30892133;chr6:30891995..30892121;chr6:30892001..30892107 26863196 MeRIP-seq:(Medium) rs1394499954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947437,Human_RBP_ID_3968652,Human_RBP_ID_8641838,Human_RBP_ID_8905686,Human_RBP_ID_22462586,Human_RBP_ID_22746438 Human_Splice_Rec_749870,Human_Splice_Rec_749888,Human_Splice_Rec_749956,Human_Splice_Rec_750046,Human_Splice_Rec_750146,Human_Splice_Rec_750182,Human_Splice_Rec_750224,Human_Splice_Rec_750236,Human_Splice_Rec_750278,Human_Splice_Rec_750308,Human_Splice_Rec_750318,Human_Splice_Rec_750354,Human_Splice_Rec_750434,Human_Splice_Rec_750464,Human_Splice_Rec_750490,Human_Splice_Rec_750500,Human_Splice_Rec_750536,Human_Splice_Rec_750542,Human_Splice_Rec_750544,Human_Splice_Rec_750546 75370 RMVar_ID_75370 Human_SNP_ID_271802183 m1A Human chr6 - 30892420 30892420 30892420 GCACTGAGACAGCCCGGGCTCTGGGGTCCCCCAGGTTGCCCCCTAGGTTGTGGCGCATGGGCTCC GCACTGAGACAGCCCGGGCTCTGGGGTCCCCCGGGTTGCCCCCTAGGTTGTGGCGCATGGGCTCC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:30892376..30892500 26863196 MeRIP-seq:(Medium) rs1199682251 Functional Loss SNV dbSNP153 33..33 33 - - - 75371 RMVar_ID_75371 Human_SNP_ID_271802472 m1A Human chr6 + 30893322 30893322 30893322 AGCAGCCCGTGGCCAAGGCCGAGGGGAGCCCGACCGCCATCCTCATCGGCTGCCTGGTGGCCATC AGCAGCCCGTGGCCAAGGCCGAGGGGAGCCCGGCCGCCATCCTCATCGGCTGCCTGGTGGCCATC A G DDR1 Ensembl:ENSG00000204580 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30893251..30893364 26863196 MeRIP-seq:(Medium) rs1427353775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_749894,Human_Splice_Rec_749962,Human_Splice_Rec_750052,Human_Splice_Rec_750152,Human_Splice_Rec_750188,Human_Splice_Rec_750242,Human_Splice_Rec_750284,Human_Splice_Rec_750324,Human_Splice_Rec_750360,Human_Splice_Rec_750440,Human_Splice_Rec_750470,Human_Splice_Rec_750506,Human_Splice_Rec_750552,Human_Splice_Rec_750566 Human_miRNA_ID_87273,Human_miRNA_ID_694463,Human_miRNA_ID_1025055 75372 RMVar_ID_75372 Human_SNP_ID_271802807 m1A Human chr6 + 30894601 30894601 30894601 CTCATCAACAACCGCCCAGGTCCTAGAGAGCCACCCCCGTACCAGGAGCCCCGGCCTCGTGGGAA CTCATCAACAACCGCCCAGGTCCTAGAGAGCCGCCCCCGTACCAGGAGCCCCGGCCTCGTGGGAA A G DDR1 Ensembl:ENSG00000204580 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:30894551..30894675 26863196 MeRIP-seq:(Medium) rs547439435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26828180 Human_Splice_Rec_749896,Human_Splice_Rec_749897,Human_Splice_Rec_749964,Human_Splice_Rec_749965,Human_Splice_Rec_750054,Human_Splice_Rec_750055,Human_Splice_Rec_750154,Human_Splice_Rec_750155,Human_Splice_Rec_750190,Human_Splice_Rec_750191,Human_Splice_Rec_750244,Human_Splice_Rec_750245,Human_Splice_Rec_750286,Human_Splice_Rec_750287,Human_Splice_Rec_750326,Human_Splice_Rec_750327,Human_Splice_Rec_750362,Human_Splice_Rec_750363,Human_Splice_Rec_750442,Human_Splice_Rec_750443,Human_Splice_Rec_750472,Human_Splice_Rec_750473,Human_Splice_Rec_750508,Human_Splice_Rec_750509,Human_Splice_Rec_750554,Human_Splice_Rec_750555,Human_Splice_Rec_750568,Human_Splice_Rec_750569,Human_Splice_Rec_750572,Human_Splice_Rec_750573,Human_Splice_Rec_750575 75373 RMVar_ID_75373 Human_SNP_ID_271802820 m1A Human chr6 - 30894628 30894628 30894628 GGGACACAGGGAGCGGAGTGGGGCGGATTCCCACGAGGCCGGGGCTCCTGGTACGGGGGTGGCTC GGGACACAGGGAGCGGAGTGGGGCGGATTCCCTCGAGGCCGGGGCTCCTGGTACGGGGGTGGCTC T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30894577..30894701 26863196 MeRIP-seq:(Medium) rs767064139 Functional Loss SNV dbSNP153 33..33 33 - - - 75374 RMVar_ID_75374 Human_SNP_ID_271802995 m1A Human chr6 - 30895377 30895377 30895377 GCAACGCTGTCGGGAGAAGGAGGAGGGGAAACACGGGGAAGGGATGAGACTCAAGGCTAGACAGA GCAACGCTGTCGGGAGAAGGAGGAGGGGAAACGCGGGGAAGGGATGAGACTCAAGGCTAGACAGA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30895371..30895513 26863196 MeRIP-seq:(Medium) rs1390376361 Functional Loss SNV dbSNP153 33..33 33 - - - 75375 RMVar_ID_75375 Human_SNP_ID_271803869 m1A Human chr6 - 30898230 30898230 30898230 CCGGCCCTGCACACGGTAATAGTCCCCAGCATAGAGGTTCCGGCTCATGCCAAAGTCTGCGATTT CCGGCCCTGCACACGGTAATAGTCCCCAGCATGGAGGTTCCGGCTCATGCCAAAGTCTGCGATTT T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30898179..30899059 32194978 MeRIP-seq:(Medium) rs543159624 Functional Loss SNV dbSNP153 33..33 33 - - - 75376 RMVar_ID_75376 Human_SNP_ID_271806400 m1A Human chr6 - 30908280 30908280 30908280 AGATGGTGAAAAAATGCGAGGAAAAGATGGGGAAAGCAAAGAAAGATTTCACAGGCAAGAGCCCA AGATGGTGAAAAAATGCGAGGAAAAGATGGGGCAAGCAAAGAAAGATTTCACAGGCAAGAGCCCA T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30908231..30908335 26863196 MeRIP-seq:(Medium) rs1386007329 Functional Loss SNV dbSNP153 33..33 33 - - - 75377 RMVar_ID_75377 Human_SNP_ID_271806570 m1A Human chr6 - 30909157 30909155 30909157 TGAAGGGGCTTCTCACCTGAAGACAGCCAGACATGTGGCAGGGTGCCCATACAATCGGTCCAATA TGAAGGGGCTTCTCACCTGAAGACAGCCAGAC__GTGGCAGGGTGCCCATACAATCGGTCCAATA CAT C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30909107..30911233 32194978 MeRIP-seq:(Medium) rs750572930 Functional Loss DEL dbSNP153 33..34 33 - - - 75378 RMVar_ID_75378 Human_SNP_ID_271808041 m1A Human chr6 + 30914291 30914291 30914291 CCAGGGCCACGTTCCAGGGTCGGGTTTGGTGGATTCCTCAGTCCCTGCCGCCGCGGGGCGCCCTG CCAGGGCCACGTTCCAGGGTCGGGTTTGGTGGGTTCCTCAGTCCCTGCCGCCGCGGGGCGCCCTG A G AL669830.2,VARS2 Ensembl:ENSG00000288473,Ensembl:ENSG00000137411 lincRNA,Protein coding exon,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30914240..30914484 26863196 MeRIP-seq:(Medium) rs929178188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267187,Human_RBP_ID_661160,Human_RBP_ID_4911364,Human_RBP_ID_5451079,Human_RBP_ID_22106364 Human_Splice_Rec_750863,Human_Splice_Rec_750919,Human_Splice_Rec_750937 75379 RMVar_ID_75379 Human_SNP_ID_271809388 m1A Human chr6 - 30918876 30918876 30918876 CGCGAGTCGTCTGGATGAACGGCCACAGCCACATCTCCAGGCAGCGTCTCTGGCCTTGTGGTTCC CGCGAGTCGTCTGGATGAACGGCCACAGCCACGTCTCCAGGCAGCGTCTCTGGCCTTGTGGTTCC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30918764..30918915 32194978 MeRIP-seq:(Medium) rs761528624 Functional Loss SNV dbSNP153 33..33 33 - - - 75380 RMVar_ID_75380 Human_SNP_ID_271810813 m1A Human chr6 - 30923429 30923429 30923429 CATGAGTGACGAGCGAGAGCTCTCGGGTGAGGAAGCCCCGCTCACACTCCTGGGCAGCCAGGGCA CATGAGTGACGAGCGAGAGCTCTCGGGTGAGGGAGCCCCGCTCACACTCCTGGGCAGCCAGGGCA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30923378..30923529 32194978 MeRIP-seq:(Medium) rs1253252571 Functional Loss SNV dbSNP153 33..33 33 - - - 75381 RMVar_ID_75381 Human_SNP_ID_271859674 m1A Human chr6 + 31114830 31114830 31114830 GAGTTGTTGTGTCCCAGCCTTCCCAAGCTTCCAGGTGTCCCAGAAACCCAGGAAATCGAGACTCA GAGTTGTTGTGTCCCAGCCTTCCCAAGCTTCCGGGTGTCCCAGAAACCCAGGAAATCGAGACTCA A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31114780..31114891 26863196 MeRIP-seq:(Medium) rs1178311473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_751183,Human_Splice_Rec_751185,Human_Splice_Rec_751191,Human_Splice_Rec_751201,Human_Splice_Rec_751203,Human_Splice_Rec_751205,Human_Splice_Rec_751209 75382 RMVar_ID_75382 Human_SNP_ID_271860005 m1A Human chr6 + 31116145 31116145 31116145 TCCCGGATGGAGCGGCAGGGGATCTTTCCAGCACTGCTGGAGCCACAGGGCTTGGCACCAGCGGA TCCCGGATGGAGCGGCAGGGGATCTTTCCAGCGCTGCTGGAGCCACAGGGCTTGGCACCAGCGGA A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31116140..31116395 26863196 MeRIP-seq:(Medium) rs771677105 Functional Loss SNV dbSNP153 33..33 33 - - - 75383 RMVar_ID_75383 Human_SNP_ID_271860764 m1A Human chr6 + 31118119 31118119 31118119 GGCCAGACAGTGGGACCAAAGGGAAGAAGACAAAAGGCAAAACAATGGAGGGCTGAGAAGTGGAG GGCCAGACAGTGGGACCAAAGGGAAGAAGACAGAAGGCAAAACAATGGAGGGCTGAGAAGTGGAG A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31118011..31118239 26863196 MeRIP-seq:(Medium) rs182058320 Functional Loss SNV dbSNP153 33..33 33 - - - 75384 RMVar_ID_75384 Human_SNP_ID_271860768 m1A Human chr6 + 31118150 31118150 31118150 AAAAGGCAAAACAATGGAGGGCTGAGAAGTGGAGACACATATAGAAGGAGACACTGGAAAAAGAC AAAAGGCAAAACAATGGAGGGCTGAGAAGTGGGGACACATATAGAAGGAGACACTGGAAAAAGAC A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31118011..31118266 26863196 MeRIP-seq:(Medium) rs1426957171 Functional Loss SNV dbSNP153 33..33 33 - - - 75385 RMVar_ID_75385 Human_SNP_ID_271864415 m1A Human chr6 + 31133247 31133247 31133247 GCCTGGGAAGGGAAGACAGACATGAATAAATCATTGCCATAGGGTGACTGGGGTGAAGGGCGTTG GCCTGGGAAGGGAAGACAGACATGAATAAATCGTTGCCATAGGGTGACTGGGGTGAAGGGCGTTG A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31133241..31133317 26863196 MeRIP-seq:(Medium) rs896520839 Functional Loss SNV dbSNP153 33..33 33 - - - 75386 RMVar_ID_75386 Human_SNP_ID_271865602 m1A Human chr6 + 31137792 31137790 31137793 CTAAGTATGGATCTCAGGAGGGGACAGGAAATATTGAGAACACCACCTTACGGGTTCAGAATAAA CTAAGTATGGATCTCAGGAGGGGACAGGAAA___TGAGAACACCACCTTACGGGTTCAGAATAAA ATAT A PSORS1C1 Ensembl:ENSG00000204540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31137667..31137968 26863196 MeRIP-seq:(Medium) rs1297924228 Functional Loss DEL dbSNP153 32..34 33 - - - 75387 RMVar_ID_75387 Human_SNP_ID_271867194 m1A Human chr6 + 31143068 31143065 31143069 GGACACCACAGATTTCTTCTTATCCAGTAGGGAAGGAAGAACTGTCAACAGTCGCTGCTGCTTGT GGACACCACAGATTTCTTCTTATCCAGTAG____GGAAGAACTGTCAACAGTCGCTGCTGCTTGT GGGAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31143020..31143130 26863196 MeRIP-seq:(Medium) rs776386759 Functional Loss DEL dbSNP153 31..34 33 - - - 75388 RMVar_ID_75388 Human_SNP_ID_271867753 m1A Human chr6 - 31145046 31145046 31145046 TTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCAAGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAGC TTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCAGGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAGC T C CCHCR1 Ensembl:ENSG00000204536 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31144639..31145114 26863196 MeRIP-seq:(Medium) rs2073720 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17710456,Human_RBP_ID_18073388,Human_RBP_ID_19017986,Human_RBP_ID_27842411 Human_Splice_Rec_751248,Human_Splice_Rec_751282,Human_Splice_Rec_751312,Human_Splice_Rec_751348,Human_Splice_Rec_751384,Human_Splice_Rec_751418,Human_Splice_Rec_751430,Human_Splice_Rec_751464 75389 RMVar_ID_75389 Human_SNP_ID_271867754 m1A Human chr6 - 31145047 31145047 31145047 TTTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCAAGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAG TTTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCGAGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAG T C CCHCR1 Ensembl:ENSG00000204536 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31144715..31145075 26863196 MeRIP-seq:(Medium) rs745552180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17710456,Human_RBP_ID_18073388,Human_RBP_ID_19017986,Human_RBP_ID_27842411 Human_Splice_Rec_751248,Human_Splice_Rec_751282,Human_Splice_Rec_751312,Human_Splice_Rec_751348,Human_Splice_Rec_751384,Human_Splice_Rec_751418,Human_Splice_Rec_751430,Human_Splice_Rec_751464 75390 RMVar_ID_75390 Human_SNP_ID_271869037 m1A Human chr6 + 31150053 31150053 31150053 CAAGGTGCTGGGAGGGAATACCGGGAGAAAAGAGAGTGCAGTGACCTGTCCCTTCAGCTGCTTAA CAAGGTGCTGGGAGGGAATACCGGGAGAAAAGCGAGTGCAGTGACCTGTCCCTTCAGCTGCTTAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31150051..31154763 32194978 MeRIP-seq:(Medium) rs1398357417 Functional Loss SNV dbSNP153 33..33 33 - - - 75391 RMVar_ID_75391 Human_SNP_ID_271870219 m1A Human chr6 + 31154707 31154707 31154707 TCTGCTGCAGCGAGGTCTCCCGCAGGAGCCGGACCTCCTCCTCCAGCCGCCGCAGCTCTTGCAGC TCTGCTGCAGCGAGGTCTCCCGCAGGAGCCGGCCCTCCTCCTCCAGCCGCCGCAGCTCTTGCAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:31154557..31154800;chr6:31151020..31156245 26863196 MeRIP-seq:(Medium) rs759394234 Functional Loss SNV dbSNP153 33..33 33 - - - 75392 RMVar_ID_75392 Human_SNP_ID_271870220 m1A Human chr6 + 31154707 31154707 31154707 TCTGCTGCAGCGAGGTCTCCCGCAGGAGCCGGACCTCCTCCTCCAGCCGCCGCAGCTCTTGCAGC TCTGCTGCAGCGAGGTCTCCCGCAGGAGCCGGGCCTCCTCCTCCAGCCGCCGCAGCTCTTGCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:31154557..31154800;chr6:31151020..31156245 26863196 MeRIP-seq:(Medium) rs759394234 Functional Loss SNV dbSNP153 33..33 33 - - - 75393 RMVar_ID_75393 Human_SNP_ID_271870702 m1A Human chr6 + 31156695 31156695 31156695 GAGTTTATTCCAGTGAGGAAGGGTCACTAGCAAGCAAGCCTGAGAAAACGGCGTGGATGGATCCC GAGTTTATTCCAGTGAGGAAGGGTCACTAGCACGCAAGCCTGAGAAAACGGCGTGGATGGATCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31156693..31156801 26863196 MeRIP-seq:(Medium) rs775533542 Functional Loss SNV dbSNP153 33..33 33 - - - 75394 RMVar_ID_75394 Human_SNP_ID_271870762 m1A Human chr6 + 31156921 31156919 31156921 CAGAGTTGAAAGGGGCCGAGCTTGAAAGTGGGAGGGGGGAATCAGCCCAGTGGAACCTGAAGAAT CAGAGTTGAAAGGGGCCGAGCTTGAAAGTGG__GGGGGGAATCAGCCCAGTGGAACCTGAAGAAT GGA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31156901..31156925 32194978 MeRIP-seq:(Medium) rs748051628 Functional Loss DEL dbSNP153 32..33 33 - - - 75395 RMVar_ID_75395 Human_SNP_ID_271870808 m1A Human chr6 - 31157060 31157060 31157060 CAGGGGAACATAGATGGCTGGAGACAGAATCTAGAGCCTTCAAATAATGTGGAGATGTTTCCACC CAGGGGAACATAGATGGCTGGAGACAGAATCTGGAGCCTTCAAATAATGTGGAGATGTTTCCACC T C CCHCR1 Ensembl:ENSG00000204536 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31156687..31157114 26863196 MeRIP-seq:(Medium) rs1307999351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948592,Human_RBP_ID_2018319 Human_Splice_Rec_751224,Human_Splice_Rec_751225,Human_Splice_Rec_751258,Human_Splice_Rec_751259,Human_Splice_Rec_751292,Human_Splice_Rec_751293,Human_Splice_Rec_751322,Human_Splice_Rec_751323,Human_Splice_Rec_751358,Human_Splice_Rec_751359,Human_Splice_Rec_751394,Human_Splice_Rec_751395,Human_Splice_Rec_751440,Human_Splice_Rec_751441,Human_Splice_Rec_751466,Human_Splice_Rec_751467,Human_Splice_Rec_751470,Human_Splice_Rec_751471,Human_Splice_Rec_751480,Human_Splice_Rec_751481,Human_Splice_Rec_751488,Human_Splice_Rec_751489,Human_Splice_Rec_751498,Human_Splice_Rec_751499,Human_Splice_Rec_751504,Human_Splice_Rec_751505,Human_Splice_Rec_751512,Human_Splice_Rec_751513,Human_Splice_Rec_751520,Human_Splice_Rec_751521,Human_Splice_Rec_751532,Human_Splice_Rec_751533,Human_Splice_Rec_751538,Human_Splice_Rec_751539,Human_Splice_Rec_751546,Human_Splice_Rec_751547,Human_Splice_Rec_751552,Human_Splice_Rec_751553,Human_Splice_Rec_751558,Human_Splice_Rec_751559,Human_Splice_Rec_751564,Human_Splice_Rec_751565,Human_Splice_Rec_751572,Human_Splice_Rec_751573,Human_Splice_Rec_751578,Human_Splice_Rec_751584,Human_Splice_Rec_751585,Human_Splice_Rec_751590,Human_Splice_Rec_751591,Human_Splice_Rec_751594,Human_Splice_Rec_751595,Human_Splice_Rec_751600,Human_Splice_Rec_751601,Human_Splice_Rec_751603 75396 RMVar_ID_75396 Human_SNP_ID_271871078 m1A Human chr6 - 31158046 31158046 31158046 GGTACAGGGGCCAGGTGAAGGGACAGATGAAGAGATCAGAACAGCCTTAGAGCTCACGGGCTAAC GGTACAGGGGCCAGGTGAAGGGACAGATGAAGCGATCAGAACAGCCTTAGAGCTCACGGGCTAAC T G CCHCR1 Ensembl:ENSG00000204536 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31157422..31158200;chr6:31157378..31158188 26863196 MeRIP-seq:(Medium) rs9263785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949228,Human_RBP_ID_5397992,Human_RBP_ID_8215173,Human_RBP_ID_9350431,Human_RBP_ID_9437393,Human_RBP_ID_15785205,Human_RBP_ID_18957193,Human_RBP_ID_19128831 Human_Splice_Rec_751519,Human_Splice_Rec_751531,Human_Splice_Rec_751537,Human_Splice_Rec_751597 GWAS_ID_9077,GWAS_ID_9078,GWAS_ID_9079,GWAS_ID_9080,GWAS_ID_9081,GWAS_ID_9082,GWAS_ID_9083,GWAS_ID_9084,GWAS_ID_9085,GWAS_ID_9086,GWAS_ID_9087,GWAS_ID_9088,GWAS_ID_9089,GWAS_ID_9090,GWAS_ID_9091,GWAS_ID_9092,GWAS_ID_9093,GWAS_ID_9094,GWAS_ID_9095,GWAS_ID_9096,GWAS_ID_9097,GWAS_ID_9098,GWAS_ID_9099,GWAS_ID_9100,GWAS_ID_9101,GWAS_ID_9102,GWAS_ID_9103,GWAS_ID_9104,GWAS_ID_9105,GWAS_ID_9106,GWAS_ID_9107,GWAS_ID_9108,GWAS_ID_9109,GWAS_ID_9110,GWAS_ID_9111,GWAS_ID_9112,GWAS_ID_9113,GWAS_ID_9114,GWAS_ID_9115,GWAS_ID_9116,GWAS_ID_9117,GWAS_ID_9118,GWAS_ID_9119,GWAS_ID_9120,GWAS_ID_9121,GWAS_ID_9122,GWAS_ID_9123,GWAS_ID_9124 75397 RMVar_ID_75397 Human_SNP_ID_271872071 m1A Human chr6 - 31161712 31161712 31161712 ATGGAGTTTAGGATCAGTGTGGCCTTGGGGGCAGGGGAGAAGGTGCTGAGAGGCCGCTGTGGAGC ATGGAGTTTAGGATCAGTGTGGCCTTGGGGGCGGGGGAGAAGGTGCTGAGAGGCCGCTGTGGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31161663..31161737 26863196 MeRIP-seq:(Medium) rs772227079 Functional Loss SNV dbSNP153 33..33 33 - - - 75398 RMVar_ID_75398 Human_SNP_ID_271872161 m1A Human chr6 - 31161948 31161948 31161948 CTACACGGAGTTTCTTCCTGGGCTCCATAAGGACCGGTGGCGGGTTCTCAGGAGGCTCACTCTCA CTACACGGAGTTTCTTCCTGGGCTCCATAAGGTCCGGTGGCGGGTTCTCAGGAGGCTCACTCTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31161897..31161989 26863196 MeRIP-seq:(Medium) rs1236727885 Functional Loss SNV dbSNP153 33..33 33 - - - 75399 RMVar_ID_75399 Human_SNP_ID_271874541 m1A Human chr6 - 31171243 31171243 31171243 AAGAACATGGAGGTGTGGGAGTGATTCCAGACAGCTGGGATGTGCAGAGCCTGAGAGAGTGCCAG AAGAACATGGAGGTGTGGGAGTGATTCCAGACGGCTGGGATGTGCAGAGCCTGAGAGAGTGCCAG T C POU5F1 Ensembl:ENSG00000204531 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31171073..31171297 26863196 MeRIP-seq:(Medium) rs556776747 Functional Loss SNV dbSNP153 33..33 33 - - - 75400 RMVar_ID_75400 Human_SNP_ID_271876236 m1A Human chr6 + 31179336 31179336 31179336 CCCCTTCTCCAAACACCACTTAAACCACTTAAACCCTTTCATTAAACCCTTACCCTGGCCTCAAA CCCCTTCTCCAAACACCACTTAAACCACTTAATCCCTTTCATTAAACCCTTACCCTGGCCTCAAA A T RF00017-4674 RNACentral:URS000094E2D9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31179113..31179400 26863196 MeRIP-seq:(Medium) rs1303685204 Functional Loss SNV dbSNP153 33..33 33 - - - 75401 RMVar_ID_75401 Human_SNP_ID_271876237 m1A Human chr6 - 31179340 31179339 31179340 ATGGTTTGAGGCCAGGGTAAGGGTTTAATGAAAGGGTTTAAGTGGTTTAAGTGGTGTTTGGAGAA ATGGTTTGAGGCCAGGGTAAGGGTTTAATGAA_GGGTTTAAGTGGTTTAAGTGGTGTTTGGAGAA CT C POU5F1 Ensembl:ENSG00000204531 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31179141..31179421 26863196 MeRIP-seq:(Medium) rs1465606893 Functional Loss DEL dbSNP153 33..33 33 - - - 75402 RMVar_ID_75402 Human_SNP_ID_271899125 m1A Human chr6 - 31268926 31268926 31268926 CCTGTTCCAGAGAGGTGGGGCTGGATGTCTCCATCTCTGTCTCAAATTCATGGTGCACTGAGCTG CCTGTTCCAGAGAGGTGGGGCTGGATGTCTCCCTCTCTGTCTCAAATTCATGGTGCACTGAGCTG T G HLA-C Ensembl:ENSG00000204525 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31268876..31268925 32194978 MeRIP-seq:(Medium) rs1470029707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252633,Human_RBP_ID_661233,Human_RBP_ID_1046754,Human_RBP_ID_2018344,Human_RBP_ID_3806039,Human_RBP_ID_27095722 Human_miRNA_ID_136665,Human_miRNA_ID_302981 75403 RMVar_ID_75403 Human_SNP_ID_271899144 m1A Human chr6 - 31268989 31268989 31268989 ACCCCCGTGTCCACCGTGACCCCTGTCCCCACACTGACCTGTGTTCCCTCCCCGATCATCTTTCC ACCCCCGTGTCCACCGTGACCCCTGTCCCCACGCTGACCTGTGTTCCCTCCCCGATCATCTTTCC T C HLA-C Ensembl:ENSG00000204525 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31268920..31269085 26863196 MeRIP-seq:(Medium) rs562645899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252633,Human_RBP_ID_661239,Human_RBP_ID_791387,Human_RBP_ID_1111532,Human_RBP_ID_4880690,Human_RBP_ID_8641889,Human_RBP_ID_17576280,Human_RBP_ID_17663592,Human_RBP_ID_18073429,Human_RBP_ID_18862636,Human_RBP_ID_18957196,Human_RBP_ID_21221632,Human_RBP_ID_23214732,Human_RBP_ID_26535264 Human_miRNA_ID_643272 75404 RMVar_ID_75404 Human_SNP_ID_271899159 m1A Human chr6 - 31269021 31269021 31269021 TAGCATAATGTGAGGAGGTGGAGAGACAGCCCACCCCCGTGTCCACCGTGACCCCTGTCCCCACA TAGCATAATGTGAGGAGGTGGAGAGACAGCCCTCCCCCGTGTCCACCGTGACCCCTGTCCCCACA T A HLA-C Ensembl:ENSG00000204525 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:31268918..31269105;chr6:31268951..31269175 26863196,32194978 MeRIP-seq:(Medium) rs1442640325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252633,Human_RBP_ID_661239,Human_RBP_ID_791387,Human_RBP_ID_1395067,Human_RBP_ID_4880691,Human_RBP_ID_17576820,Human_RBP_ID_17663593,Human_RBP_ID_17710464,Human_RBP_ID_18073430,Human_RBP_ID_18957196,Human_RBP_ID_21221632,Human_RBP_ID_23214732,Human_RBP_ID_26541062,Human_RBP_ID_27095723 Human_miRNA_ID_1705503 75405 RMVar_ID_75405 Human_SNP_ID_271900334 m1A Human chr6 + 31271130 31271129 31271130 GTTCTCCAGGTATCTGCGGAGCCACTCCACGCACGTGCCCTCCAGGTAGGCTCTCAGCTGCTCCG GTTCTCCAGGTATCTGCGGAGCCACTCCACGC_CGTGCCCTCCAGGTAGGCTCTCAGCTGCTCCG CA C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31271101..31271175;chr6:31271051..31271175;chr6:31271067..31271175 26863196 MeRIP-seq:(Medium) rs773980967 Functional Loss DEL dbSNP153 33..33 33 - - - 75406 RMVar_ID_75406 Human_SNP_ID_271900338 m1A Human chr6 + 31271130 31271130 31271130 GTTCTCCAGGTATCTGCGGAGCCACTCCACGCACGTGCCCTCCAGGTAGGCTCTCAGCTGCTCCG GTTCTCCAGGTATCTGCGGAGCCACTCCACGCCCGTGCCCTCCAGGTAGGCTCTCAGCTGCTCCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31271101..31271175;chr6:31271051..31271175;chr6:31271067..31271175 26863196 MeRIP-seq:(Medium) rs41562916 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9125 75407 RMVar_ID_75407 Human_SNP_ID_271900349 m1A Human chr6 - 31271133 31271133 31271133 CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCACGTGCGTGGAGTGGCTCCGCAGATACCTGGAG CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCGCGTGCGTGGAGTGGCTCCGCAGATACCTGGAG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31271076..31271175 26863196 MeRIP-seq:(Medium) rs1050685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252636,Human_RBP_ID_661253,Human_RBP_ID_791391,Human_RBP_ID_4880719,Human_RBP_ID_17663600,Human_RBP_ID_22461056,Human_RBP_ID_22773381 Human_Splice_Rec_751687,Human_Splice_Rec_751701,Human_Splice_Rec_751715,Human_Splice_Rec_751729,Human_Splice_Rec_751743,Human_Splice_Rec_751755,Human_Splice_Rec_751759 75408 RMVar_ID_75408 Human_SNP_ID_271900350 m1A Human chr6 - 31271133 31271133 31271133 CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCACGTGCGTGGAGTGGCTCCGCAGATACCTGGAG CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCCCGTGCGTGGAGTGGCTCCGCAGATACCTGGAG T G HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31271076..31271175 26863196 MeRIP-seq:(Medium) rs1050685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252636,Human_RBP_ID_661253,Human_RBP_ID_791391,Human_RBP_ID_4880719,Human_RBP_ID_17663600,Human_RBP_ID_22461056,Human_RBP_ID_22773381 Human_Splice_Rec_751687,Human_Splice_Rec_751701,Human_Splice_Rec_751715,Human_Splice_Rec_751729,Human_Splice_Rec_751743,Human_Splice_Rec_751755,Human_Splice_Rec_751759 75409 RMVar_ID_75409 Human_SNP_ID_271900356 m1A Human chr6 - 31271138 31271138 31271138 CCGTGCGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCACGTGCGTGGAGTGGCTCCGCAGATACC CCGTGCGGCGGAGCAGCTGAGAGCCTACCTGGTGGGCACGTGCGTGGAGTGGCTCCGCAGATACC T A HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31271051..31271176;chr6:31271051..31271375 26863196 MeRIP-seq:(Medium) rs75032224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252636,Human_RBP_ID_661253,Human_RBP_ID_791391,Human_RBP_ID_17663600,Human_RBP_ID_22461056,Human_RBP_ID_22773381 Human_Splice_Rec_751687,Human_Splice_Rec_751701,Human_Splice_Rec_751715,Human_Splice_Rec_751729,Human_Splice_Rec_751743,Human_Splice_Rec_751755,Human_Splice_Rec_751759 75410 RMVar_ID_75410 Human_SNP_ID_271900419 m1A Human chr6 - 31271177 31271177 31271177 CACCGCGGCTCAGATCACCCAGCGCAAGTTGGAGGCGGCCCGTGCGGCGGAGCAGCTGAGAGCCT CACCGCGGCTCAGATCACCCAGCGCAAGTTGGGGGCGGCCCGTGCGGCGGAGCAGCTGAGAGCCT T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31271051..31271223 26863410 MeRIP-seq:(Medium) rs281860509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661255,Human_RBP_ID_22773381 75411 RMVar_ID_75411 Human_SNP_ID_271900574 m1A Human chr6 - 31271276 31271276 31271276 GCCCGACGGGCGCCTCCTCCGCGGGTATGACCAGTCCGCCTACGACGGCAAGGATTACATCGCCC GCCCGACGGGCGCCTCCTCCGCGGGTATGACCGGTCCGCCTACGACGGCAAGGATTACATCGCCC T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31271226..31271351 26863196 MeRIP-seq:(Medium) rs281860469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18472041,Human_RBP_ID_22461057,Human_RBP_ID_22773383,Human_RBP_ID_27095739 Human_Splice_Rec_751700,Human_Splice_Rec_751714,Human_Splice_Rec_751728,Human_Splice_Rec_751742,Human_Splice_Rec_751754,Human_Splice_Rec_751758 75412 RMVar_ID_75412 Human_SNP_ID_271900579 m1A Human chr6 - 31271279 31271279 31271279 GGGGCCCGACGGGCGCCTCCTCCGCGGGTATGACCAGTCCGCCTACGACGGCAAGGATTACATCG GGGGCCCGACGGGCGCCTCCTCCGCGGGTATGTCCAGTCCGCCTACGACGGCAAGGATTACATCG T A HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr6:31271229..31271347;chr6:31269476..31353935 26863196,32194978 MeRIP-seq:(Medium) rs41542424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18472041,Human_RBP_ID_22461057,Human_RBP_ID_22773383,Human_RBP_ID_27095739 Human_Splice_Rec_751700,Human_Splice_Rec_751714,Human_Splice_Rec_751728,Human_Splice_Rec_751742,Human_Splice_Rec_751754,Human_Splice_Rec_751758 75413 RMVar_ID_75413 Human_SNP_ID_271900580 m1A Human chr6 - 31271279 31271279 31271279 GGGGCCCGACGGGCGCCTCCTCCGCGGGTATGACCAGTCCGCCTACGACGGCAAGGATTACATCG GGGGCCCGACGGGCGCCTCCTCCGCGGGTATGGCCAGTCCGCCTACGACGGCAAGGATTACATCG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr6:31271229..31271347;chr6:31269476..31353935 26863196,32194978 MeRIP-seq:(Medium) rs41542424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18472041,Human_RBP_ID_22461057,Human_RBP_ID_22773383,Human_RBP_ID_27095739 Human_Splice_Rec_751700,Human_Splice_Rec_751714,Human_Splice_Rec_751728,Human_Splice_Rec_751742,Human_Splice_Rec_751754,Human_Splice_Rec_751758 75414 RMVar_ID_75414 Human_SNP_ID_271900971 m1A Human chr6 - 31271655 31271655 31271655 CCGGGAGACACAGAAGTACAAGCGCCAGGCACAGGCTGACCGAGTGAGCCTGCGGAACCTGCGCG CCGGGAGACACAGAAGTACAAGCGCCAGGCACCGGCTGACCGAGTGAGCCTGCGGAACCTGCGCG T G HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs45500292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8641900,Human_RBP_ID_22773385 Human_Splice_Rec_751699,Human_Splice_Rec_751713,Human_Splice_Rec_751727,Human_Splice_Rec_751741,Human_Splice_Rec_751753,Human_Splice_Rec_751757 75415 RMVar_ID_75415 Human_SNP_ID_271901005 m1A Human chr6 - 31271678 31271678 31271678 CAGGAGGGGCCGGAGTATTGGGACCGGGAGACACAGAAGTACAAGCGCCAGGCACAGGCTGACCG CAGGAGGGGCCGGAGTATTGGGACCGGGAGACGCAGAAGTACAAGCGCCAGGCACAGGCTGACCG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31271506..31272125 26863196 MeRIP-seq:(Medium) rs41555917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82019,Human_RBP_ID_791393,Human_RBP_ID_1046755,Human_RBP_ID_1142410,Human_RBP_ID_1670654,Human_RBP_ID_4911461,Human_RBP_ID_5617757,Human_RBP_ID_8641900,Human_RBP_ID_17710473,Human_RBP_ID_18472042,Human_RBP_ID_18862640,Human_RBP_ID_22461058,Human_RBP_ID_22773386 Human_Splice_Rec_751699,Human_Splice_Rec_751713,Human_Splice_Rec_751727,Human_Splice_Rec_751741,Human_Splice_Rec_751753,Human_Splice_Rec_751757 75416 RMVar_ID_75416 Human_SNP_ID_271901019 m1A Human chr6 - 31271688 31271688 31271688 GTGGGTGGAGCAGGAGGGGCCGGAGTATTGGGACCGGGAGACACAGAAGTACAAGCGCCAGGCAC GTGGGTGGAGCAGGAGGGGCCGGAGTATTGGGGCCGGGAGACACAGAAGTACAAGCGCCAGGCAC T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31271601..31272125;chr6:31271601..31271875 26863196 MeRIP-seq:(Medium) rs281860393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82019,Human_RBP_ID_791393,Human_RBP_ID_1046755,Human_RBP_ID_1670654,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_18862640,Human_RBP_ID_22461058,Human_RBP_ID_22773386 Human_Splice_Rec_751699,Human_Splice_Rec_751713,Human_Splice_Rec_751727,Human_Splice_Rec_751741,Human_Splice_Rec_751753,Human_Splice_Rec_751757 75417 RMVar_ID_75417 Human_SNP_ID_271901023 m1A Human chr6 + 31271693 31271693 31271693 TGGCGCTTGTACTTCTGTGTCTCCCGGTCCCAATACTCCGGCCCCTCCTGCTCCACCCACGGCGC TGGCGCTTGTACTTCTGTGTCTCCCGGTCCCACTACTCCGGCCCCTCCTGCTCCACCCACGGCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31271523..31272125 26863196 MeRIP-seq:(Medium) rs281860389 Functional Loss SNV dbSNP153 33..33 33 - - - 75418 RMVar_ID_75418 Human_SNP_ID_271901024 m1A Human chr6 + 31271693 31271693 31271693 TGGCGCTTGTACTTCTGTGTCTCCCGGTCCCAATACTCCGGCCCCTCCTGCTCCACCCACGGCGC TGGCGCTTGTACTTCTGTGTCTCCCGGTCCCAGTACTCCGGCCCCTCCTGCTCCACCCACGGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31271523..31272125 26863196 MeRIP-seq:(Medium) rs281860389 Functional Loss SNV dbSNP153 33..33 33 - - - 75419 RMVar_ID_75419 Human_SNP_ID_271901047 m1A Human chr6 - 31271709 31271707 31271710 GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGAGGGGCCGGAGTATTGGGACCGGGAGACAC GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAG___GAGGGGCCGGAGTATTGGGACCGGGAGACAC CCTG C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31271576..31271725 32194978 MeRIP-seq:(Medium) rs281860378 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_252638,Human_RBP_ID_661259,Human_RBP_ID_791393,Human_RBP_ID_4911464,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_22461058,Human_RBP_ID_22773387 75420 RMVar_ID_75420 Human_SNP_ID_271901051 m1A Human chr6 - 31271709 31271709 31271709 GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGAGGGGCCGGAGTATTGGGACCGGGAGACAC GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCTGGAGGGGCCGGAGTATTGGGACCGGGAGACAC T A HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31271576..31271725 32194978 MeRIP-seq:(Medium) rs281860379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252638,Human_RBP_ID_661259,Human_RBP_ID_791393,Human_RBP_ID_4911464,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_22461058,Human_RBP_ID_22773387 75421 RMVar_ID_75421 Human_SNP_ID_271901052 m1A Human chr6 - 31271709 31271709 31271709 GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGAGGGGCCGGAGTATTGGGACCGGGAGACAC GAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCGGGAGGGGCCGGAGTATTGGGACCGGGAGACAC T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31271576..31271725 32194978 MeRIP-seq:(Medium) rs281860379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252638,Human_RBP_ID_661259,Human_RBP_ID_791393,Human_RBP_ID_4911464,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_22461058,Human_RBP_ID_22773387 75422 RMVar_ID_75422 Human_SNP_ID_271901083 m1A Human chr6 - 31271738 31271736 31271738 GTGCGGTTCGACAGCGACGCCGCGAGTCCGAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGA GTGCGGTTCGACAGCGACGCCGCGAGTCCGAG__GGGAGCCGCGGGCGCCGTGGGTGGAGCAGGA CCT C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:31271638..31271737 26863410 MeRIP-seq:(Medium) rs753232182 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4880737,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_22405216,Human_RBP_ID_22461058,Human_RBP_ID_22773388 75423 RMVar_ID_75423 Human_SNP_ID_271901088 m1A Human chr6 - 31271738 31271738 31271738 GTGCGGTTCGACAGCGACGCCGCGAGTCCGAGAGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGA GTGCGGTTCGACAGCGACGCCGCGAGTCCGAGGGGGGAGCCGCGGGCGCCGTGGGTGGAGCAGGA T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:31271638..31271737 26863410 MeRIP-seq:(Medium) rs72558131 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4880737,Human_RBP_ID_18084741,Human_RBP_ID_18472042,Human_RBP_ID_22405216,Human_RBP_ID_22461058,Human_RBP_ID_22773388 75424 RMVar_ID_75424 Human_SNP_ID_271901178 m1A Human chr6 - 31271814 31271814 31271814 CGACACCGCCGTGTCCCGGCCCGGCCGCGGAGAGCCCCGCTTCATCTCAGTGGGCTACGTGGACG CGACACCGCCGTGTCCCGGCCCGGCCGCGGAGTGCCCCGCTTCATCTCAGTGGGCTACGTGGACG T A HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs281860339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252639,Human_RBP_ID_661260,Human_RBP_ID_791394,Human_RBP_ID_4903178,Human_RBP_ID_9193457,Human_RBP_ID_22461059,Human_RBP_ID_27095743 Human_Splice_Rec_751698,Human_Splice_Rec_751712,Human_Splice_Rec_751726,Human_Splice_Rec_751740,Human_Splice_Rec_751752,Human_Splice_Rec_751762 75425 RMVar_ID_75425 Human_SNP_ID_271901297 m1A Human chr6 - 31271870 31271870 31271870 GGTCGGGCGGGTCTCAGCCCCTCCTCGCCCCCAGGCTCCCACTCCATGAGGTATTTCGACACCGC GGTCGGGCGGGTCTCAGCCCCTCCTCGCCCCCGGGCTCCCACTCCATGAGGTATTTCGACACCGC T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31271576..31272100 26863410 MeRIP-seq:(Medium) rs1562029398 Functional Loss SNV dbSNP153 33..33 33 - - - 75426 RMVar_ID_75426 Human_SNP_ID_271901412 m1A Human chr6 + 31272032 31272032 31272032 GGCCCAGGTCTCGGTCAGGGCCAGGCCTCCCGAGAGCAGCAGGAGGAGGGCTCGGGGCGCCATGA GGCCCAGGTCTCGGTCAGGGCCAGGCCTCCCGGGAGCAGCAGGAGGAGGGCTCGGGGCGCCATGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:31271801..31272033 26863410 MeRIP-seq:(Medium) rs1157292832 Functional Loss SNV dbSNP153 33..33 33 - - - 75427 RMVar_ID_75427 Human_SNP_ID_271903650 m1A Human chr6 + 31280505 31280505 31280505 ATGACCCACATCGTGCGGGAAGTCGACAGGCCAGGATCCAAGGTGAACAAGAAGGAGGTGGTGGA ATGACCCACATCGTGCGGGAAGTCGACAGGCCGGGATCCAAGGTGAACAAGAAGGAGGTGGTGGA A G RPL3P2 Ensembl:ENSG00000227939 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879023901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4911480,Human_RBP_ID_8270520,Human_RBP_ID_26541064,Human_RBP_ID_27095750 75428 RMVar_ID_75428 Human_SNP_ID_271923600 m1A Human chr6 - 31355467 31355466 31355468 CACTGACCTGGCAGCGGGATGGCGAGGACCAAACTCAGGACACTGAGCTTGTGGAGACCAGACCA CACTGACCTGGCAGCGGGATGGCGAGGACCA__CTCAGGACACTGAGCTTGTGGAGACCAGACCA GTT G HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31355326..31355525;chr6:31355213..31355614 26863196 MeRIP-seq:(Medium) rs1317836901 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_172924,Human_RBP_ID_252756,Human_RBP_ID_661287,Human_RBP_ID_791551,Human_RBP_ID_5617758,Human_RBP_ID_18086145,Human_RBP_ID_22461066,Human_RBP_ID_22773394,Human_RBP_ID_27161090,Human_RBP_ID_27523183 75429 RMVar_ID_75429 Human_SNP_ID_271923669 m1A Human chr6 - 31355577 31355577 31355577 CTGACTCTTCCCATCAGACCCCCCAAAGACACACGTGACCCACCACCCCATCTCTGACCATGAGG CTGACTCTTCCCATCAGACCCCCCAAAGACACGCGTGACCCACCACCCCATCTCTGACCATGAGG T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31355526..31355600 26863196 MeRIP-seq:(Medium) rs45610732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18073440,Human_RBP_ID_22773903 Human_Splice_Rec_751778,Human_Splice_Rec_751792,Human_Splice_Rec_751806,Human_Splice_Rec_751810 75430 RMVar_ID_75430 Human_SNP_ID_271923995 m1A Human chr6 + 31356153 31356153 31356153 CGGCGACCTATAGGAGATGGGGAAGGCTCCCCACTGCCCCTGGTACCAGCGCGCTCCAGCTTGTC CGGCGACCTATAGGAGATGGGGAAGGCTCCCCCCTGCCCCTGGTACCAGCGCGCTCCAGCTTGTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356151..31356200 26863196 MeRIP-seq:(Medium) rs45529836 Functional Loss SNV dbSNP153 33..33 33 - - - 75431 RMVar_ID_75431 Human_SNP_ID_271924186 m1A Human chr6 - 31356259 31356259 31356259 GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGTGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG T A HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31356151..31356450 32194978 MeRIP-seq:(Medium) rs151341293 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17663950,Human_RBP_ID_18472044,Human_RBP_ID_22461067,Human_RBP_ID_22773395,Human_RBP_ID_24156743 Human_Splice_Rec_751777,Human_Splice_Rec_751791,Human_Splice_Rec_751805,Human_Splice_Rec_751809 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75432 RMVar_ID_75432 Human_SNP_ID_271924187 m1A Human chr6 - 31356259 31356259 31356259 GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGCGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG T G HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31356151..31356450 32194978 MeRIP-seq:(Medium) rs151341293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17663950,Human_RBP_ID_18472044,Human_RBP_ID_22461067,Human_RBP_ID_22773395,Human_RBP_ID_24156743 Human_Splice_Rec_751777,Human_Splice_Rec_751791,Human_Splice_Rec_751805,Human_Splice_Rec_751809 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75433 RMVar_ID_75433 Human_SNP_ID_271924215 m1A Human chr6 + 31356275 31356275 31356275 TCTCCGCTGCTCCGCCTCACGGGCCGCCTCCCACTTGCGCTGGGTGATCTGAGCCGCCGTGTCCG TCTCCGCTGCTCCGCCTCACGGGCCGCCTCCCGCTTGCGCTGGGTGATCTGAGCCGCCGTGTCCG A G NONHSAG043472.2 RNACentral:URS00008BD4E9 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31356176..31356499 26863410 MeRIP-seq:(Medium) rs151341287 Functional Loss SNV dbSNP153 33..33 33 - - - 75434 RMVar_ID_75434 Human_SNP_ID_271924233 m1A Human chr6 - 31356287 31356285 31356287 CCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG CCTGGACCGCCGCGGACACGGCGGCTCAGATC__CCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG GGT G HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356226..31356468;chr6:31356226..31356499 26863196 MeRIP-seq:(Medium) rs1387796482 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2867548 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75435 RMVar_ID_75435 Human_SNP_ID_271924237 m1A Human chr6 - 31356287 31356287 31356287 CCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG CCTGGACCGCCGCGGACACGGCGGCTCAGATCTCCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG T A HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356226..31356468;chr6:31356226..31356499 26863196 MeRIP-seq:(Medium) rs41541519 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2867548 GWAS_ID_9126 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75436 RMVar_ID_75436 Human_SNP_ID_271924238 m1A Human chr6 - 31356287 31356287 31356287 CCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG CCTGGACCGCCGCGGACACGGCGGCTCAGATCGCCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356226..31356468;chr6:31356226..31356499 26863196 MeRIP-seq:(Medium) rs41541519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2867548 GWAS_ID_9126 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75437 RMVar_ID_75437 Human_SNP_ID_271924247 m1A Human chr6 - 31356292 31356292 31356292 GCGCTCCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTG GCGCTCCTGGACCGCCGCGGACACGGCGGCTCGGATCACCCAGCGCAAGTGGGAGGCGGCCCGTG T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31356203..31356485 26863196 MeRIP-seq:(Medium) rs151341266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2403458 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75438 RMVar_ID_75438 Human_SNP_ID_271924248 m1A Human chr6 - 31356292 31356292 31356292 GCGCTCCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTG GCGCTCCTGGACCGCCGCGGACACGGCGGCTCCGATCACCCAGCGCAAGTGGGAGGCGGCCCGTG T G HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31356203..31356485 26863196 MeRIP-seq:(Medium) rs151341266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2403458 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75439 RMVar_ID_75439 Human_SNP_ID_271924343 m1A Human chr6 - 31356352 31356352 31356352 CCGCGGGCATGACCAGTACGCCTACGACGGCAAGGATTACATCGCCCTGAACGAGGACCTGCGCT CCGCGGGCATGACCAGTACGCCTACGACGGCAGGGATTACATCGCCCTGAACGAGGACCTGCGCT T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31356301..31356375 26863196 MeRIP-seq:(Medium) rs281864619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773397 Human_Splice_Rec_751776,Human_Splice_Rec_751790,Human_Splice_Rec_751808,Human_Splice_Rec_751812 Human_miRNA_ID_2353114,Human_miRNA_ID_2489978,Human_miRNA_ID_2561911,Human_miRNA_ID_2752065 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 75440 RMVar_ID_75440 Human_SNP_ID_271924959 m1A Human chr6 - 31356783 31356783 31356783 GGCGCCGTGGATAGAGCAGGAGGGGCCGGAGTATTGGGACCGGAACACACAGATCTACAAGGCCC GGCGCCGTGGATAGAGCAGGAGGGGCCGGAGTTTTGGGACCGGAACACACAGATCTACAAGGCCC T A HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356659..31356994;chr6:31356611..31357225 26863196 MeRIP-seq:(Medium) rs41560117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_751775,Human_Splice_Rec_751789,Human_Splice_Rec_751807,Human_Splice_Rec_751811 75441 RMVar_ID_75441 Human_SNP_ID_271924997 m1A Human chr6 - 31356805 31356805 31356805 CGAGTCCGAGAGAGGAGCCGCGGGCGCCGTGGATAGAGCAGGAGGGGCCGGAGTATTGGGACCGG CGAGTCCGAGAGAGGAGCCGCGGGCGCCGTGGGTAGAGCAGGAGGGGCCGGAGTATTGGGACCGG T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:31356647..31356865;chr6:31356695..31356994 26863196 MeRIP-seq:(Medium) rs145974360 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_661288,Human_RBP_ID_24156744 75442 RMVar_ID_75442 Human_SNP_ID_271925114 m1A Human chr6 + 31356861 31356861 31356861 TCGGACTCGCGGCGTCGCTGTCGAACCTCACGAACTGGGTGTCGTCCACGTAGCCCACTGAGATG TCGGACTCGCGGCGTCGCTGTCGAACCTCACGGACTGGGTGTCGTCCACGTAGCCCACTGAGATG A G AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:31356676..31356994;chr6:31356676..31356975 32194978 MeRIP-seq:(Medium) rs281864595 Functional Loss SNV dbSNP153 33..33 33 - - - 75443 RMVar_ID_75443 Human_SNP_ID_271925227 m1A Human chr6 + 31356938 31356938 31356938 CCGCGGCCGGGCCGGGACACGGAGGTGTAGAAATACCTCATGGAGTGGGAGCCTGGGGGTGAGGA CCGCGGCCGGGCCGGGACACGGAGGTGTAGAACTACCTCATGGAGTGGGAGCCTGGGGGTGAGGA A C AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31356744..31356994 26863410 MeRIP-seq:(Medium) rs41546617 Functional Loss SNV dbSNP153 33..33 33 - - - 75444 RMVar_ID_75444 Human_SNP_ID_271925228 m1A Human chr6 + 31356938 31356938 31356938 CCGCGGCCGGGCCGGGACACGGAGGTGTAGAAATACCTCATGGAGTGGGAGCCTGGGGGTGAGGA CCGCGGCCGGGCCGGGACACGGAGGTGTAGAAGTACCTCATGGAGTGGGAGCCTGGGGGTGAGGA A G AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31356744..31356994 26863410 MeRIP-seq:(Medium) rs41546617 Functional Loss SNV dbSNP153 33..33 33 - - - 75445 RMVar_ID_75445 Human_SNP_ID_271925254 m1A Human chr6 - 31356959 31356959 31356959 GGTCGGGCGGGTCTCAGCCCCTCCTCACCCCCAGGCTCCCACTCCATGAGGTATTTCTACACCTC GGTCGGGCGGGTCTCAGCCCCTCCTCACCCCCGGGCTCCCACTCCATGAGGTATTTCTACACCTC T C HLA-B Ensembl:ENSG00000234745 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31356876..31356975 26863196 MeRIP-seq:(Medium) rs151341086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904643 Human_miRNA_ID_96818 75446 RMVar_ID_75446 Human_SNP_ID_271925378 m1A Human chr6 + 31357074 31357074 31357074 CGCTCCTCCCGGCAGAGGCCATTTCCCTCCCGACCCGCACTCACCGGCCCAGGTCTCGGTCAGGG CGCTCCTCCCGGCAGAGGCCATTTCCCTCCCGCCCCGCACTCACCGGCCCAGGTCTCGGTCAGGG A C AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31357072..31357200 26863196 MeRIP-seq:(Medium) rs1489678122 Functional Loss SNV dbSNP153 33..33 33 - - - 75447 RMVar_ID_75447 Human_SNP_ID_271925390 m1A Human chr6 + 31357080 31357080 31357080 TCCCGGCAGAGGCCATTTCCCTCCCGACCCGCACTCACCGGCCCAGGTCTCGGTCAGGGCCAGGG TCCCGGCAGAGGCCATTTCCCTCCCGACCCGCCCTCACCGGCCCAGGTCTCGGTCAGGGCCAGGG A C AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:31357076..31357175 32194978 MeRIP-seq:(Medium) rs45539837 Functional Loss SNV dbSNP153 33..33 33 - - - 75448 RMVar_ID_75448 Human_SNP_ID_271939039 m1A Human chr6 + 31411333 31411333 31411333 AGACTGCCTGCAGGAACTACGGCGATATCTAGAATCCGGCGTAGTCCTGAGGAGAACAGGTACCG AGACTGCCTGCAGGAACTACGGCGATATCTAGGATCCGGCGTAGTCCTGAGGAGAACAGGTACCG A G AL645933.5,MICA Ensembl:ENSG00000288587,Ensembl:ENSG00000204520 lincRNA,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31411183..31411333 32194978 MeRIP-seq:(Medium) rs1445245203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5619492,Human_RBP_ID_9400247,Human_RBP_ID_19016600 Human_Splice_Rec_751826,Human_Splice_Rec_751827,Human_Splice_Rec_751835,Human_Splice_Rec_751857 75449 RMVar_ID_75449 Human_SNP_ID_271956599 m1A Human chr6 + 31471789 31471789 31471789 GACAAAATAGGGGTGTGCAGAGCCTTGTGGGGATGTGAATGCAGGGTGTTTGGGGGACCCAGTGT GACAAAATAGGGGTGTGCAGAGCCTTGTGGGGGTGTGAATGCAGGGTGTTTGGGGGACCCAGTGT A G HCP5 Ensembl:ENSG00000206337 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31471786..31471887 26863196 MeRIP-seq:(Medium) rs897060551 Functional Loss SNV dbSNP153 33..33 33 - - - 75450 RMVar_ID_75450 Human_SNP_ID_271964859 m1A Human chr6 - 31505873 31505873 31505873 GCCTCCCATTACTCTTGCCCCTGCCGACTCTCACCTCCTTTCTGGTCCTTGATATGAGTCAGGGT GCCTCCCATTACTCTTGCCCCTGCCGACTCTCGCCTCCTTTCTGGTCCTTGATATGAGTCAGGGT T C lnc-ATP6V1G2-DDX39B-2,lnc-BBS5-6 RNACentral:URS00008BC637,RNACentral:URS0000E2127A lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31505824..31506096 26863196 MeRIP-seq:(Medium) rs760165805 Functional Loss SNV dbSNP153 33..33 33 - - - 75451 RMVar_ID_75451 Human_SNP_ID_271965256 m1A Human chr6 + 31507202 31507202 31507202 GGATGTCCTGCCTGATGGGAATGGAACCTACCAGACCTGGGTGGCCACCAGGATTCGCCAAGGAG GGATGTCCTGCCTGATGGGAATGGAACCTACCGGACCTGGGTGGCCACCAGGATTCGCCAAGGAG A G MICB Ensembl:ENSG00000204516 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31507151..31507275 32194978 MeRIP-seq:(Medium) rs1315464581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24156846 Human_Splice_Rec_751907,Human_Splice_Rec_751917,Human_Splice_Rec_751927,Human_Splice_Rec_751933 RMVar_hsa_circ_121505,RMVar_hsa_circ_237824 75452 RMVar_ID_75452 Human_SNP_ID_271970540 m1A Human chr6 - 31530334 31530334 31530334 AGACACTACTGCCCCCACCCCTGACAGCCCCCACCCCATGGCTTCCATCTTTTGCATCACCACCA AGACACTACTGCCCCCACCCCTGACAGCCCCCCCCCCATGGCTTCCATCTTTTGCATCACCACCA T G DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31530226..31530484 26863196 MeRIP-seq:(Medium) rs1317297468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661322,Human_RBP_ID_1670673,Human_RBP_ID_18073471,Human_RBP_ID_18450132,Human_RBP_ID_18862682,Human_RBP_ID_22513993,Human_RBP_ID_23060018,Human_RBP_ID_27523207 75453 RMVar_ID_75453 Human_SNP_ID_271970543 m1A Human chr6 - 31530350 31530350 31530350 AGGGTGGGGGTGAAGGAGACACTACTGCCCCCACCCCTGACAGCCCCCACCCCATGGCTTCCATC AGGGTGGGGGTGAAGGAGACACTACTGCCCCCCCCCCTGACAGCCCCCACCCCATGGCTTCCATC T G DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding exon,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31530301..31530375 26863196 MeRIP-seq:(Medium) rs1440410294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661322,Human_RBP_ID_4911510,Human_RBP_ID_8641959,Human_RBP_ID_17710481,Human_RBP_ID_18073471,Human_RBP_ID_22310944,Human_RBP_ID_22831096,Human_RBP_ID_23060020 75454 RMVar_ID_75454 Human_SNP_ID_271970556 m1A Human chr6 + 31530401 31530400 31530402 TTCACCCCCACCCTGGTGTCCTCTCCTGAAGGACAGACGGTCACATTCCAAAATGGGCGAGTCTT TTCACCCCCACCCTGGTGTCCTCTCCTGAAGG__AGACGGTCACATTCCAAAATGGGCGAGTCTT GAC G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31530301..31530425 26863196 MeRIP-seq:(Medium) rs1163358168 Functional Loss DEL dbSNP153 33..34 33 - - - 75455 RMVar_ID_75455 Human_SNP_ID_271970795 m1A Human chr6 - 31531278 31531278 31531278 GCCCCAGGAGGAGAGGTGAGCTGAAGATGGGAAAGATATTTTGTGTCCTTGGGAGAAAAAGACAG GCCCCAGGAGGAGAGGTGAGCTGAAGATGGGACAGATATTTTGTGTCCTTGGGAGAAAAAGACAG T G DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31531276..31531300 26863196 MeRIP-seq:(Medium) rs1419220656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25996138 75456 RMVar_ID_75456 Human_SNP_ID_271970818 m1A Human chr6 + 31531394 31531394 31531394 GCCAAGGCAATGCACCGCTGCACAGACTTCACAAAGATCACCACCTGTTGTGGGGTGGGGTGGGG GCCAAGGCAATGCACCGCTGCACAGACTTCACGAAGATCACCACCTGTTGTGGGGTGGGGTGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31531269..31531475 26863196 MeRIP-seq:(Medium) rs529970580 Functional Loss SNV dbSNP153 33..33 33 - - - 75457 RMVar_ID_75457 Human_SNP_ID_271971081 m1A Human chr6 + 31532501 31532501 31532501 GACTCAAGTGATCCACCTCCCTCAGCCTCCCCAAGTGCTGGGATTACACACATAAGCCACCGTGC GACTCAAGTGATCCACCTCCCTCAGCCTCCCCGAGTGCTGGGATTACACACATAAGCCACCGTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31532497..31532584 26863196 MeRIP-seq:(Medium) rs1047600976 Functional Loss SNV dbSNP153 33..33 33 - - - 75458 RMVar_ID_75458 Human_SNP_ID_271971809 m1A Human chr6 - 31535276 31535276 31535276 TCGCCCTCTTCCTCAGACTCCCTTGTCATTCAAGTGCCAAGAAGGCGGCTTGTGCCCAACTGGGA TCGCCCTCTTCCTCAGACTCCCTTGTCATTCAGGTGCCAAGAAGGCGGCTTGTGCCCAACTGGGA T C DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31535251..31535275 26863196 MeRIP-seq:(Medium) rs1562413341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326867,Human_RBP_ID_1670781,Human_RBP_ID_4881059,Human_RBP_ID_15785856,Human_RBP_ID_17091155,Human_RBP_ID_18073524,Human_RBP_ID_18862760,Human_RBP_ID_18957207,Human_RBP_ID_21324098,Human_RBP_ID_22831148,Human_RBP_ID_25996338,Human_RBP_ID_27095872 75459 RMVar_ID_75459 Human_SNP_ID_271972624 m1A Human chr6 + 31538850 31538850 31538850 GCCAACTCCCGAGTGTGACACATCACCAGTACAGACACCTTAGGCAGGAAGTAGACGGAGACATA GCCAACTCCCGAGTGTGACACATCACCAGTACGGACACCTTAGGCAGGAAGTAGACGGAGACATA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31536551..31539268 26863410 MeRIP-seq:(Medium) rs1462271309 Functional Loss SNV dbSNP153 33..33 33 - - - 75460 RMVar_ID_75460 Human_SNP_ID_271973108 m1A Human chr6 + 31540612 31540611 31540612 CGCAAAATAGGTGAAAACAAGGGGTGAAGAGTAGGGGATTGAGGAACAGCAAAGGAAAACAAAGA CGCAAAATAGGTGAAAACAAGGGGTGAAGAGT_GGGGATTGAGGAACAGCAAAGGAAAACAAAGA TA T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:31540561..31540674 26863196 MeRIP-seq:(Medium) rs1309067987 Functional Loss DEL dbSNP153 33..33 33 - - - 75461 RMVar_ID_75461 Human_SNP_ID_271973550 m1A Human chr6 - 31541874 31541874 31541874 TCCGCACCCATCCCGTCACATGGGTTCCTGATACCCTTTTCACAGGCGATGGTCTGGTCGCTGGG TCCGCACCCATCCCGTCACATGGGTTCCTGATGCCCTTTTCACAGGCGATGGTCTGGTCGCTGGG T C DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31541872..31542025 26863196 MeRIP-seq:(Medium) rs1452760037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15786197,Human_RBP_ID_19133507,Human_RBP_ID_21324236,Human_RBP_ID_24436260 Human_Splice_Rec_752101 75462 RMVar_ID_75462 Human_SNP_ID_271973707 m1A Human chr6 - 31542250 31542249 31542250 AAGAGATGAGGGGCATGGAGAGGAGTAGGATAAGAGAATAAAGATAACAGTGGGGGGGAGACGTT AAGAGATGAGGGGCATGGAGAGGAGTAGGATA_GAGAATAAAGATAACAGTGGGGGGGAGACGTT CT C DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31542201..31542708 26863196 MeRIP-seq:(Medium) rs1445407249 Functional Loss DEL dbSNP153 33..33 33 - - - 75463 RMVar_ID_75463 Human_SNP_ID_271974494 m1A Human chr6 - 31545568 31545568 31545568 CCCTCTCCCTACCCCCCAGGCCATGGGCTCCCAGGGGAACCTGTCTGCTGAGGTGGAGCAGGCTA CCCTCTCCCTACCCCCCAGGCCATGGGCTCCCGGGGGAACCTGTCTGCTGAGGTGGAGCAGGCTA T C ATP6V1G2,ATP6V1G2-DDX39B Ensembl:ENSG00000213760,Ensembl:ENSG00000254870 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31545559..31545834 26863196 MeRIP-seq:(Medium) rs762530469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_752194,Human_Splice_Rec_752198,Human_Splice_Rec_752202,Human_Splice_Rec_752206 75464 RMVar_ID_75464 Human_SNP_ID_271974630 m1A Human chr6 - 31546188 31546188 31546188 TCTGCCTCCAGGGAAGGCCCGGCGACTGAAGCAGGCAAAGGAGGAGGCACAGATGGAGGTGGAGC TCTGCCTCCAGGGAAGGCCCGGCGACTGAAGCCGGCAAAGGAGGAGGCACAGATGGAGGTGGAGC T G ATP6V1G2,ATP6V1G2-DDX39B Ensembl:ENSG00000213760,Ensembl:ENSG00000254870 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31546082..31546551 26863196 MeRIP-seq:(Medium) rs373793437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_752150,Human_Splice_Rec_752151,Human_Splice_Rec_752174,Human_Splice_Rec_752175,Human_Splice_Rec_752180,Human_Splice_Rec_752181,Human_Splice_Rec_752190,Human_Splice_Rec_752192,Human_Splice_Rec_752193,Human_Splice_Rec_752196,Human_Splice_Rec_752197,Human_Splice_Rec_752200,Human_Splice_Rec_752201,Human_Splice_Rec_752204,Human_Splice_Rec_752208 75465 RMVar_ID_75465 Human_SNP_ID_271975200 m1A Human chr6 - 31548186 31548186 31548186 CGAAAGCGACGTTCTCGGCGTTGGCGGCGGGAAGTGGAGGCCATGGAACTCTTGGGCTGGGGAAG CGAAAGCGACGTTCTCGGCGTTGGCGGCGGGATGTGGAGGCCATGGAACTCTTGGGCTGGGGAAG T A ATP6V1G2 Ensembl:ENSG00000213760 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31547639..31548398 26863196 MeRIP-seq:(Medium) rs539358080 Functional Loss SNV dbSNP153 33..33 33 - - - 75466 RMVar_ID_75466 Human_SNP_ID_271977415 m1A Human chr6 + 31557802 31557801 31557803 CTCCAAGGAGCGGGAATGGAGACAGAAGCTCCAGGGTGAGCTGGAGGACGAGTGGCAGGAAGTCA CTCCAAGGAGCGGGAATGGAGACAGAAGCTCC__GGTGAGCTGGAGGACGAGTGGCAGGAAGTCA CAG C NFKBIL1 Ensembl:ENSG00000204498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31557601..31557878 26863196 MeRIP-seq:(Medium) rs776614833 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_752213,Human_Splice_Rec_752219,Human_Splice_Rec_752225 75467 RMVar_ID_75467 Human_SNP_ID_271977585 m1A Human chr6 + 31558223 31558223 31558223 GCAGCGGCTCTTCAGGGAGCGAGCCCGGGCCAAGGAGGAAGAGCTGCGTGAGAGCCGAGCCAGGA GCAGCGGCTCTTCAGGGAGCGAGCCCGGGCCAGGGAGGAAGAGCTGCGTGAGAGCCGAGCCAGGA A G NFKBIL1 Ensembl:ENSG00000204498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31558001..31558825 26863196 MeRIP-seq:(Medium) rs1169152699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661437,Human_RBP_ID_5152080,Human_RBP_ID_19018030,Human_RBP_ID_23067512 75468 RMVar_ID_75468 Human_SNP_ID_271977592 m1A Human chr6 + 31558243 31558243 31558243 GAGCCCGGGCCAAGGAGGAAGAGCTGCGTGAGAGCCGAGCCAGGAGGGCGCAGGAGGCTCTAGGG GAGCCCGGGCCAAGGAGGAAGAGCTGCGTGAGCGCCGAGCCAGGAGGGCGCAGGAGGCTCTAGGG A C NFKBIL1 Ensembl:ENSG00000204498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31558041..31558775 26863196 MeRIP-seq:(Medium) rs753854522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661437,Human_RBP_ID_5152080,Human_RBP_ID_19016621,Human_RBP_ID_23067512 75469 RMVar_ID_75469 Human_SNP_ID_271992923 m1A Human chr6 + 31620314 31620314 31620314 GTGTGTCGTTGCCTTCCACTTTTGGCGTCCCAACGTCTCTCCGCTCCCATCTTTCTACTAACGTC GTGTGTCGTTGCCTTCCACTTTTGGCGTCCCAGCGTCTCTCCGCTCCCATCTTTCTACTAACGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31620064..31620369;chr6:31620107..31620361 26863196 MeRIP-seq:(Medium) rs945427603 Functional Loss SNV dbSNP153 33..33 33 - - - 75470 RMVar_ID_75470 Human_SNP_ID_271993136 m1A Human chr6 + 31620772 31620767 31620773 CGAGGGAGACGGGAGGAGCCGAACCCGGCGCCATCCGCCGCCATCCTCCCCCGCCCCACCGCCAT CGAGGGAGACGGGAGGAGCCGAACCCGG______CCGCCGCCATCCTCCCCCGCCCCACCGCCAT GCGCCAT G PRRC2A Ensembl:ENSG00000204469 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:31620701..31621033;chr6:31620726..31620920 26863196 MeRIP-seq:(Medium) rs1261205020 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_792346,Human_RBP_ID_4903186,Human_RBP_ID_5151811,Human_RBP_ID_5451094,Human_RBP_ID_9336050,Human_RBP_ID_18073573,Human_RBP_ID_27095916 Human_Splice_Rec_752447,Human_Splice_Rec_752507,Human_Splice_Rec_752567 75471 RMVar_ID_75471 Human_SNP_ID_271993136 m1A Human chr6 - 31620773 31620767 31620773 GATGGCGGTGGGGCGGGGGAGGATGGCGGCGGATGGCGCCGGGTTCGGCTCCTCCCGTCTCCCTC GATGGCGGTGGGGCGGGGGAGGATGGCGGCGG______CCGGGTTCGGCTCCTCCCGTCTCCCTC GCGCCAT G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr6:31620726..31620930;chr6:31620726..31620942;chr6:31620751..31620775 26863196,32194978 MeRIP-seq:(Medium) rs1261205020 Functional Loss DEL dbSNP153 33..38 33 - - - 75472 RMVar_ID_75472 Human_SNP_ID_271993146 m1A Human chr6 - 31620786 31620786 31620786 CTCCCCGGGACGGGATGGCGGTGGGGCGGGGGAGGATGGCGGCGGATGGCGCCGGGTTCGGCTCC CTCCCCGGGACGGGATGGCGGTGGGGCGGGGGGGGATGGCGGCGGATGGCGCCGGGTTCGGCTCC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31620751..31620914 26863196 MeRIP-seq:(Medium) rs996678709 Functional Loss SNV dbSNP153 33..33 33 - - - 75473 RMVar_ID_75473 Human_SNP_ID_271993170 m1A Human chr6 + 31620849 31620849 31620849 AGCCCCTAGGCCCGGGTCCCGGATCCCCGCGCACCCGGCCAGGTGAGTCTGGGTGAACCGTGCGC AGCCCCTAGGCCCGGGTCCCGGATCCCCGCGCGCCCGGCCAGGTGAGTCTGGGTGAACCGTGCGC A G PRRC2A Ensembl:ENSG00000204469 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31620726..31620906;chr6:31620826..31620850 26863196 MeRIP-seq:(Medium) rs1386520912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252593,Human_RBP_ID_4903187,Human_RBP_ID_5327378,Human_RBP_ID_8905208,Human_RBP_ID_9309159,Human_RBP_ID_22461836 Human_Splice_Rec_752447,Human_Splice_Rec_752507,Human_Splice_Rec_752567 75474 RMVar_ID_75474 Human_SNP_ID_271993823 m1A Human chr6 - 31622717 31622717 31622717 CCTCCCCCAAAACGTGCCAGAGCCTGTGGGCCAGACAGCAAGTGTCTCAGTCTCTGTCCCCTGTA CCTCCCCCAAAACGTGCCAGAGCCTGTGGGCCGGACAGCAAGTGTCTCAGTCTCTGTCCCCTGTA T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31622701..31622775 26863196 MeRIP-seq:(Medium) rs543397473 Functional Loss SNV dbSNP153 33..33 33 - - - 75475 RMVar_ID_75475 Human_SNP_ID_271993833 m1A Human chr6 + 31622764 31622764 31622764 GGCACGTTTTGGGGGAGGTGCCTGCAGGACCCAACATACTCAATGAGCTTCCAGCGCAATGTCCG GGCACGTTTTGGGGGAGGTGCCTGCAGGACCCGACATACTCAATGAGCTTCCAGCGCAATGTCCG A G PRRC2A Ensembl:ENSG00000204469 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31622751..31622775 26863196 MeRIP-seq:(Medium) rs1460398002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046812,Human_RBP_ID_1217189,Human_RBP_ID_1670859,Human_RBP_ID_2018482,Human_RBP_ID_3806214,Human_RBP_ID_4881203,Human_RBP_ID_5428405,Human_RBP_ID_5511425,Human_RBP_ID_7592473,Human_RBP_ID_8642070,Human_RBP_ID_8899991,Human_RBP_ID_9308213,Human_RBP_ID_15786393,Human_RBP_ID_17306483,Human_RBP_ID_17419616,Human_RBP_ID_17535588,Human_RBP_ID_17710499,Human_RBP_ID_18073575,Human_RBP_ID_18450160,Human_RBP_ID_18862849,Human_RBP_ID_21221660,Human_RBP_ID_22831185,Human_RBP_ID_23293953,Human_RBP_ID_27095919 Human_Splice_Rec_752448,Human_Splice_Rec_752508 75476 RMVar_ID_75476 Human_SNP_ID_271993860 m1A Human chr6 + 31622851 31622851 31622851 GGGAAAGGATGGAAAGAAGTATTCCTCGCTCAACCTGTTTGATACGTATAAGGGCAAGTCCTTAG GGGAAAGGATGGAAAGAAGTATTCCTCGCTCAGCCTGTTTGATACGTATAAGGGCAAGTCCTTAG A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31622645..31622943 26863196 MeRIP-seq:(Medium) rs1169794411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1670862,Human_RBP_ID_2018482,Human_RBP_ID_3806215,Human_RBP_ID_15786399,Human_RBP_ID_18073576,Human_RBP_ID_18862850,Human_RBP_ID_21221661,Human_RBP_ID_22832789,Human_RBP_ID_27345489 Human_Splice_Rec_752449,Human_Splice_Rec_752509 75477 RMVar_ID_75477 Human_SNP_ID_271994205 m1A Human chr6 + 31623850 31623850 31623850 GCCGAGAACAAAGGCAATGACCCCAATGTCTCACTAGTGCCAAAAGACGGAACAGGATGGGCAAG GCCGAGAACAAAGGCAATGACCCCAATGTCTCGCTAGTGCCAAAAGACGGAACAGGATGGGCAAG A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31623826..31623850 26863196 MeRIP-seq:(Medium) rs749404040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1217195,Human_RBP_ID_1326879,Human_RBP_ID_1670872,Human_RBP_ID_2018488,Human_RBP_ID_3806217,Human_RBP_ID_4911639,Human_RBP_ID_8642082,Human_RBP_ID_8900004,Human_RBP_ID_18862859,Human_RBP_ID_22831192,Human_RBP_ID_24157059,Human_RBP_ID_26828194,Human_RBP_ID_27095929,Human_RBP_ID_27754918 Human_Splice_Rec_752451,Human_Splice_Rec_752511 Human_miRNA_ID_141022 75478 RMVar_ID_75478 Human_SNP_ID_271994331 m1A Human chr6 + 31624314 31624314 31624314 GCCGCCGGAATCGCAGCCACTGCCGGCTTCACAGACGCCTGCCTCCAACCAGCCGAAACGACCCC GCCGCCGGAATCGCAGCCACTGCCGGCTTCACCGACGCCTGCCTCCAACCAGCCGAAACGACCCC A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31624251..31624375 26863196 MeRIP-seq:(Medium) rs769504407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252596,Human_RBP_ID_661460,Human_RBP_ID_1046814,Human_RBP_ID_8642086,Human_RBP_ID_8900007,Human_RBP_ID_17306484,Human_RBP_ID_18073578,Human_RBP_ID_18862861,Human_RBP_ID_23060240 Human_Splice_Rec_752452,Human_Splice_Rec_752453,Human_Splice_Rec_752512,Human_Splice_Rec_752513,Human_Splice_Rec_752568,Human_Splice_Rec_752569 75479 RMVar_ID_75479 Human_SNP_ID_271994892 m1A Human chr6 + 31625907 31625907 31625907 AGCAATCCAGGTCTGGGTTTGTGGCTGGGGGCAGGGGAAGCTTATTGGGGGAGGAGATGGTTTTC AGCAATCCAGGTCTGGGTTTGTGGCTGGGGGCGGGGGAAGCTTATTGGGGGAGGAGATGGTTTTC A G PRRC2A Ensembl:ENSG00000204469 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31625904..31626050 26863196 MeRIP-seq:(Medium) rs1449719739 Functional Loss SNV dbSNP153 33..33 33 - - - 75480 RMVar_ID_75480 Human_SNP_ID_271994930 m1A Human chr6 - 31626003 31626003 31626003 CACACGGGGAAAACGGCTGTACACAAAAAAGAAAATGAAATATGGCATGTTGTATAACCACATGC CACACGGGGAAAACGGCTGTACACAAAAAAGAGAATGAAATATGGCATGTTGTATAACCACATGC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr6:31626001..31626050 26863196 MeRIP-seq:(Medium) rs200630465 Functional Loss SNV dbSNP153 33..33 33 - - - 75481 RMVar_ID_75481 Human_SNP_ID_271994976 m1A Human chr6 + 31626103 31626103 31626103 AGTAGAGCCTGTGGGTCGTCCCTCTATTCTCAAAGAGGATAATCTCAAAGAGTTTGATCAGTTGG AGTAGAGCCTGTGGGTCGTCCCTCTATTCTCAGAGAGGATAATCTCAAAGAGTTTGATCAGTTGG A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31626001..31626150 26863196 MeRIP-seq:(Medium) rs942144296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046820,Human_RBP_ID_1217197,Human_RBP_ID_1670883,Human_RBP_ID_2018500,Human_RBP_ID_3806224,Human_RBP_ID_4881251,Human_RBP_ID_8900023,Human_RBP_ID_15786495,Human_RBP_ID_17306492,Human_RBP_ID_17535593,Human_RBP_ID_17710501,Human_RBP_ID_18073586,Human_RBP_ID_18862873,Human_RBP_ID_21221665,Human_RBP_ID_22831202,Human_RBP_ID_27095952,Human_RBP_ID_27523286 Human_Splice_Rec_752462,Human_Splice_Rec_752463,Human_Splice_Rec_752522,Human_Splice_Rec_752523,Human_Splice_Rec_752578,Human_Splice_Rec_752579,Human_Splice_Rec_752583 75482 RMVar_ID_75482 Human_SNP_ID_271995536 m1A Human chr6 - 31627859 31627859 31627859 CTTCTCGCCGTCGCCGGGCCCGCTCCACTGCCAGGGAAATCTCAGATGACGACTGCTTTCGTCGC CTTCTCGCCGTCGCCGGGCCCGCTCCACTGCCGGGGAAATCTCAGATGACGACTGCTTTCGTCGC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31627751..31628200 26863196 MeRIP-seq:(Medium) rs780687130 Functional Loss SNV dbSNP153 33..33 33 - - - 75483 RMVar_ID_75483 Human_SNP_ID_271995619 m1A Human chr6 - 31628057 31628057 31628057 CTGATGCTGGAGGTGGAGCTGGAGGTGCAGGGAGTTCTTTAGGGACTGCAGGTGGTGGAGCTGGG CTGATGCTGGAGGTGGAGCTGGAGGTGCAGGGTGTTCTTTAGGGACTGCAGGTGGTGGAGCTGGG T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31627826..31628125 26863196 MeRIP-seq:(Medium) rs1006323055 Functional Loss SNV dbSNP153 33..33 33 - - - 75484 RMVar_ID_75484 Human_SNP_ID_271996211 m1A Human chr6 + 31629740 31629740 31629740 GTGCTCTGGGCCGGCCCCCACCCATGCCCCCAATGAACTTTGATCCCCGATGGATGATGATTCCT GTGCTCTGGGCCGGCCCCCACCCATGCCCCCACTGAACTTTGATCCCCGATGGATGATGATTCCT A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31629641..31629800 26863410 MeRIP-seq:(Medium) rs770097771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661482,Human_RBP_ID_1670920,Human_RBP_ID_2018528,Human_RBP_ID_3806237,Human_RBP_ID_5219182,Human_RBP_ID_7592530,Human_RBP_ID_8642134,Human_RBP_ID_8900061,Human_RBP_ID_15786610,Human_RBP_ID_18862907,Human_RBP_ID_18958138,Human_RBP_ID_22534075,Human_RBP_ID_24157075,Human_RBP_ID_27345524,Human_RBP_ID_27523312 75485 RMVar_ID_75485 Human_SNP_ID_271996212 m1A Human chr6 + 31629740 31629740 31629740 GTGCTCTGGGCCGGCCCCCACCCATGCCCCCAATGAACTTTGATCCCCGATGGATGATGATTCCT GTGCTCTGGGCCGGCCCCCACCCATGCCCCCAGTGAACTTTGATCCCCGATGGATGATGATTCCT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31629641..31629800 26863410 MeRIP-seq:(Medium) rs770097771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661482,Human_RBP_ID_1670920,Human_RBP_ID_2018528,Human_RBP_ID_3806237,Human_RBP_ID_5219182,Human_RBP_ID_7592530,Human_RBP_ID_8642134,Human_RBP_ID_8900061,Human_RBP_ID_15786610,Human_RBP_ID_18862907,Human_RBP_ID_18958138,Human_RBP_ID_22534075,Human_RBP_ID_24157075,Human_RBP_ID_27345524,Human_RBP_ID_27523312 75486 RMVar_ID_75486 Human_SNP_ID_271996590 m1A Human chr6 + 31630725 31630725 31630725 ATCCAAAGTTGGCCTGGGTAGGAGATGTCTTCACCGCCACACCCGCTGAACCCCGCCCACTTACC ATCCAAAGTTGGCCTGGGTAGGAGATGTCTTCCCCGCCACACCCGCTGAACCCCGCCCACTTACC A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31630592..31630740 26863196 MeRIP-seq:(Medium) rs77461161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661488,Human_RBP_ID_1670930,Human_RBP_ID_2018533,Human_RBP_ID_3806239,Human_RBP_ID_3968711,Human_RBP_ID_8642137,Human_RBP_ID_8900073,Human_RBP_ID_9262952,Human_RBP_ID_9309592,Human_RBP_ID_17421991,Human_RBP_ID_18073612,Human_RBP_ID_18195401,Human_RBP_ID_18862920,Human_RBP_ID_23060328,Human_RBP_ID_27523321 Human_Splice_Rec_752475,Human_Splice_Rec_752535 75487 RMVar_ID_75487 Human_SNP_ID_271996626 m1A Human chr6 + 31630800 31630800 31630800 GCCAGGCTGCGGATGAGGATGACAAGGGGATGAGGTGAGTCTTGGTCATGAGAAATGGGTGAGTT GCCAGGCTGCGGATGAGGATGACAAGGGGATGGGGTGAGTCTTGGTCATGAGAAATGGGTGAGTT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31630776..31630800;chr6:31630776..31630825 26863196 MeRIP-seq:(Medium) rs749871641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8900074,Human_RBP_ID_9309594 Human_Splice_Rec_752475,Human_Splice_Rec_752535 75488 RMVar_ID_75488 Human_SNP_ID_271996798 m1A Human chr6 - 31631283 31631283 31631283 GGTGGTGGAGTTTGTATCTTGGCCACTTCATCACTGCCTGGGGGCCAGGGGAGTGGACGGGGCCC GGTGGTGGAGTTTGTATCTTGGCCACTTCATCGCTGCCTGGGGGCCAGGGGAGTGGACGGGGCCC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31629218..31631610 32194978 MeRIP-seq:(Medium) rs762429188 Functional Loss SNV dbSNP153 33..33 33 - - - 75489 RMVar_ID_75489 Human_SNP_ID_271996806 m1A Human chr6 + 31631310 31631310 31631310 GGCAGTGATGAAGTGGCCAAGATACAAACTCCACCACCCAAGAAGGAGCCCCCTAAGGAGGAGAC GGCAGTGATGAAGTGGCCAAGATACAAACTCCGCCACCCAAGAAGGAGCCCCCTAAGGAGGAGAC A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:31631301..31631325 26863196 MeRIP-seq:(Medium) rs1561819421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046836,Human_RBP_ID_1326886,Human_RBP_ID_1670934,Human_RBP_ID_2018536,Human_RBP_ID_3806241,Human_RBP_ID_4881337,Human_RBP_ID_8144492,Human_RBP_ID_8900082,Human_RBP_ID_9262782,Human_RBP_ID_9308228,Human_RBP_ID_17306511,Human_RBP_ID_17419630,Human_RBP_ID_17535605,Human_RBP_ID_18073617,Human_RBP_ID_18370200,Human_RBP_ID_18539061,Human_RBP_ID_22514032,Human_RBP_ID_22534165,Human_RBP_ID_27096017,Human_RBP_ID_27345531,Human_RBP_ID_27523328,Human_RBP_ID_27568356 75490 RMVar_ID_75490 Human_SNP_ID_271996873 m1A Human chr6 + 31631425 31631425 31631425 GGAGTGGAGGCCAGGGCCCCCCACCACCACGCAGAGAGAGTCGCACAGAGACCCGCTGGGGCCCT GGAGTGGAGGCCAGGGCCCCCCACCACCACGCCGAGAGAGTCGCACAGAGACCCGCTGGGGCCCT A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31631376..31631425 26863196 MeRIP-seq:(Medium) rs778566221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27096017 75491 RMVar_ID_75491 Human_SNP_ID_271996913 m1A Human chr6 + 31631495 31631495 31631495 AGGGAGCAGTCGTCGTGGAATCCCTCCAGAGGAGCCAGGGGCCCCACCCCGCCGGGCTGGGCCTA AGGGAGCAGTCGTCGTGGAATCCCTCCAGAGGCGCCAGGGGCCCCACCCCGCCGGGCTGGGCCTA A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31631451..31631575 26863196 MeRIP-seq:(Medium) rs1286639959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252614,Human_RBP_ID_792361,Human_RBP_ID_4881342,Human_RBP_ID_5532360,Human_RBP_ID_9309170,Human_RBP_ID_17306512,Human_RBP_ID_18195406,Human_RBP_ID_22104852,Human_RBP_ID_22534166,Human_RBP_ID_22728342,Human_RBP_ID_23060337 Human_miRNA_ID_338245,Human_miRNA_ID_731295,Human_miRNA_ID_795540,Human_miRNA_ID_1705604 75492 RMVar_ID_75492 Human_SNP_ID_271996929 m1A Human chr6 - 31631526 31631526 31631526 TCTACTTTTGTAGGTGGTGGAGGTTTCTTTATAGGCCCAGCCCGGCGGGGTGGGGCCCCTGGCTC TCTACTTTTGTAGGTGGTGGAGGTTTCTTTATCGGCCCAGCCCGGCGGGGTGGGGCCCCTGGCTC T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31631138..31631678 26863196 MeRIP-seq:(Medium) rs766486273 Functional Loss SNV dbSNP153 33..33 33 - - - 75493 RMVar_ID_75493 Human_SNP_ID_271997089 m1A Human chr6 + 31631839 31631839 31631839 GAGGGCGGGGAGCCCGAAGCCGGGAATTCCGCAGTTACCGAGAGTTTCGAGGAGATGATGGGCGT GAGGGCGGGGAGCCCGAAGCCGGGAATTCCGCCGTTACCGAGAGTTTCGAGGAGATGATGGGCGT A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:31631148..31632550;chr6:31631746..31632148 26863196 MeRIP-seq:(Medium) rs757311627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285014,Human_RBP_ID_2018544,Human_RBP_ID_3806244,Human_RBP_ID_3968713,Human_RBP_ID_8237094,Human_RBP_ID_8642147,Human_RBP_ID_8900097,Human_RBP_ID_9309172,Human_RBP_ID_15786641,Human_RBP_ID_17535607,Human_RBP_ID_18195408,Human_RBP_ID_22105780,Human_RBP_ID_22311099,Human_RBP_ID_22728138,Human_RBP_ID_24554611,Human_RBP_ID_26353639,Human_RBP_ID_27096022,Human_RBP_ID_27345539 75494 RMVar_ID_75494 Human_SNP_ID_271997090 m1A Human chr6 + 31631839 31631839 31631839 GAGGGCGGGGAGCCCGAAGCCGGGAATTCCGCAGTTACCGAGAGTTTCGAGGAGATGATGGGCGT GAGGGCGGGGAGCCCGAAGCCGGGAATTCCGCGGTTACCGAGAGTTTCGAGGAGATGATGGGCGT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:31631148..31632550;chr6:31631746..31632148 26863196 MeRIP-seq:(Medium) rs757311627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285014,Human_RBP_ID_2018544,Human_RBP_ID_3806244,Human_RBP_ID_3968713,Human_RBP_ID_8237094,Human_RBP_ID_8642147,Human_RBP_ID_8900097,Human_RBP_ID_9309172,Human_RBP_ID_15786641,Human_RBP_ID_17535607,Human_RBP_ID_18195408,Human_RBP_ID_22105780,Human_RBP_ID_22311099,Human_RBP_ID_22728138,Human_RBP_ID_24554611,Human_RBP_ID_26353639,Human_RBP_ID_27096022,Human_RBP_ID_27345539 75495 RMVar_ID_75495 Human_SNP_ID_271997198 m1A Human chr6 - 31632045 31632045 31632045 ACCTGGGTGAGTGTTCCCTCCTTGGGTGTGGGAGCCTCCTTGTCTGAAGGAGCCAGATCACTCTC ACCTGGGTGAGTGTTCCCTCCTTGGGTGTGGGGGCCTCCTTGTCTGAAGGAGCCAGATCACTCTC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31632026..31632050 26863196 MeRIP-seq:(Medium) rs1156432329 Functional Loss SNV dbSNP153 33..33 33 - - - 75496 RMVar_ID_75496 Human_SNP_ID_271997324 m1A Human chr6 - 31632234 31632234 31632234 GGAGGTTTCTTGGGAGCCAGAGACTTGGCTGGAGGGCTCCAGCCTGGGCAAACTTGAGGAGGGGG GGAGGTTTCTTGGGAGCCAGAGACTTGGCTGGCGGGCTCCAGCCTGGGCAAACTTGAGGAGGGGG T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31632201..31632275 26863196 MeRIP-seq:(Medium) rs754666563 Functional Loss SNV dbSNP153 33..33 33 - - - 75497 RMVar_ID_75497 Human_SNP_ID_271997411 m1A Human chr6 - 31632381 31632381 31632381 CTCCCATGTCGCCTCCTTCGGGGTCGCTCCCCATCTTCCATGCCCACATTGCTACCTCCATTGCT CTCCCATGTCGCCTCCTTCGGGGTCGCTCCCCGTCTTCCATGCCCACATTGCTACCTCCATTGCT T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31631726..31633014 26863196 MeRIP-seq:(Medium) rs763588833 Functional Loss SNV dbSNP153 33..33 33 - - - 75498 RMVar_ID_75498 Human_SNP_ID_271997885 m1A Human chr6 - 31633379 31633377 31633380 GGAAGCCCCGGGGGACGCTCCTCTGGAGGACGACTGGAGAAAACAGAGCATTAGCTCCAGTATCC GGAAGCCCCGGGGGACGCTCCTCTGGAGGAC___TGGAGAAAACAGAGCATTAGCTCCAGTATCC AGTC A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31633376..31633587 26863196 MeRIP-seq:(Medium) rs1263523236 Functional Loss DEL dbSNP153 32..34 33 - - - 75499 RMVar_ID_75499 Human_SNP_ID_271998697 m1A Human chr6 - 31635385 31635385 31635385 TACCACTAGGCGTAAGTCTGAGTCCTGTGATCACAAGAAGGCAGGAGACATTGTCCCGTGACAGA TACCACTAGGCGTAAGTCTGAGTCCTGTGATCTCAAGAAGGCAGGAGACATTGTCCCGTGACAGA T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31635382..31635483 32194978 MeRIP-seq:(Medium) rs1389809497 Functional Loss SNV dbSNP153 33..33 33 - - - 75500 RMVar_ID_75500 Human_SNP_ID_271999166 m1A Human chr6 - 31636579 31636579 31636579 TACCTGCTGGGCAGGAGCCCCTGAAGGGAGAAAGCCACTTTGGCCACCAGGCTGCAGAGGAGTAG TACCTGCTGGGCAGGAGCCCCTGAAGGGAGAATGCCACTTTGGCCACCAGGCTGCAGAGGAGTAG T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31636508..31636615;chr6:31636501..31636600 26863196 MeRIP-seq:(Medium) rs763750945 Functional Loss SNV dbSNP153 33..33 33 - - - 75501 RMVar_ID_75501 Human_SNP_ID_271999177 m1A Human chr6 + 31636611 31636611 31636611 TTTCTCCCTTCAGGGGCTCCTGCCCAGCAGGTATATTGTATCTTCACACTTCCCCTTCATTTGAT TTTCTCCCTTCAGGGGCTCCTGCCCAGCAGGTGTATTGTATCTTCACACTTCCCCTTCATTTGAT A G PRRC2A Ensembl:ENSG00000204469 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31636601..31636625 26863196 MeRIP-seq:(Medium) rs1381874012 Functional Loss SNV dbSNP153 33..33 33 - - - 75502 RMVar_ID_75502 Human_SNP_ID_271999246 m1A Human chr6 + 31636792 31636792 31636792 CTGCCTGTGGTGAACTTTGGCTCCCTGCCGCCAGCACCACCTCCTGCCCCACCTCCCCTTTCTCT CTGCCTGTGGTGAACTTTGGCTCCCTGCCGCCGGCACCACCTCCTGCCCCACCTCCCCTTTCTCT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31636619..31636950 26863196 MeRIP-seq:(Medium) rs780464569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791380,Human_RBP_ID_8900199,Human_RBP_ID_15786690,Human_RBP_ID_17421996,Human_RBP_ID_17537859,Human_RBP_ID_18862987,Human_RBP_ID_18958142,Human_RBP_ID_21324581,Human_RBP_ID_27345582 Human_Splice_Rec_752500,Human_Splice_Rec_752560,Human_Splice_Rec_752606,Human_Splice_Rec_752612 75503 RMVar_ID_75503 Human_SNP_ID_271999250 m1A Human chr6 - 31636801 31636798 31636801 ACAGGTAACAGAGAAAGGGGAGGTGGGGCAGGAGGTGGTGCTGGCGGCAGGGAGCCAAAGTTCAC ACAGGTAACAGAGAAAGGGGAGGTGGGGCAGG___TGGTGCTGGCGGCAGGGAGCCAAAGTTCAC ACCT A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31636751..31636935 26863196 MeRIP-seq:(Medium) rs1410944055 Functional Loss DEL dbSNP153 33..35 33 - - - 75504 RMVar_ID_75504 Human_SNP_ID_271999263 m1A Human chr6 - 31636833 31636833 31636833 CAGCCAGGCTGGGGGGCTGCAGAGCAGGGCCCACAGGTAACAGAGAAAGGGGAGGTGGGGCAGGA CAGCCAGGCTGGGGGGCTGCAGAGCAGGGCCCGCAGGTAACAGAGAAAGGGGAGGTGGGGCAGGA T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31636788..31636881 26863196 MeRIP-seq:(Medium) rs369842092 Functional Loss SNV dbSNP153 33..33 33 - - - 75505 RMVar_ID_75505 Human_SNP_ID_271999386 m1A Human chr6 + 31637116 31637116 31637116 CTGAGCAGCAACCTTGGGGGACCTGGATCATCACGGACTCCCCCAACTGGAAGGTGAAACGGAAT CTGAGCAGCAACCTTGGGGGACCTGGATCATCGCGGACTCCCCCAACTGGAAGGTGAAACGGAAT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31637026..31637150 32194978 MeRIP-seq:(Medium) rs767776808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661534,Human_RBP_ID_948116,Human_RBP_ID_1046859,Human_RBP_ID_2018590,Human_RBP_ID_3806275,Human_RBP_ID_3968732,Human_RBP_ID_5121891,Human_RBP_ID_8642201,Human_RBP_ID_8900203,Human_RBP_ID_17306548,Human_RBP_ID_17419651,Human_RBP_ID_17535634,Human_RBP_ID_18195433,Human_RBP_ID_22773038,Human_RBP_ID_23214738 Human_Splice_Rec_752502,Human_Splice_Rec_752503,Human_Splice_Rec_752562,Human_Splice_Rec_752563,Human_Splice_Rec_752608,Human_Splice_Rec_752609,Human_Splice_Rec_752613,Human_Splice_Rec_752615 75506 RMVar_ID_75506 Human_SNP_ID_271999457 m1A Human chr6 - 31637285 31637285 31637285 TAAAGGTCGACGCGCTGGGTGCGGAAGACTCCACTGTAGGTGGAAGGCGTGGCCTTGAGACGGGA TAAAGGTCGACGCGCTGGGTGCGGAAGACTCCCCTGTAGGTGGAAGGCGTGGCCTTGAGACGGGA T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:31637226..31637325;chr6:31636726..31637325 32194978 MeRIP-seq:(Medium) rs1195661779 Functional Loss SNV dbSNP153 33..33 33 - - - 75507 RMVar_ID_75507 Human_SNP_ID_271999483 m1A Human chr6 - 31637326 31637326 31637326 TTTAGAGTTGGGGCCACAAGGGTTTCTCCTTCACCTGCTGGTAAAGGTCGACGCGCTGGGTGCGG TTTAGAGTTGGGGCCACAAGGGTTTCTCCTTCTCCTGCTGGTAAAGGTCGACGCGCTGGGTGCGG T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31637276..31637325 26863196 MeRIP-seq:(Medium) rs113248917 Functional Loss SNV dbSNP153 33..33 33 - - - 75508 RMVar_ID_75508 Human_SNP_ID_271999484 m1A Human chr6 - 31637326 31637326 31637326 TTTAGAGTTGGGGCCACAAGGGTTTCTCCTTCACCTGCTGGTAAAGGTCGACGCGCTGGGTGCGG TTTAGAGTTGGGGCCACAAGGGTTTCTCCTTCGCCTGCTGGTAAAGGTCGACGCGCTGGGTGCGG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31637276..31637325 26863196 MeRIP-seq:(Medium) rs113248917 Functional Loss SNV dbSNP153 33..33 33 - - - 75509 RMVar_ID_75509 Human_SNP_ID_271999500 m1A Human chr6 - 31637355 31637355 31637355 AAGGACAGGAAATCAGGTGGCAACTCGAATTTAGAGTTGGGGCCACAAGGGTTTCTCCTTCACCT AAGGACAGGAAATCAGGTGGCAACTCGAATTTGGAGTTGGGGCCACAAGGGTTTCTCCTTCACCT T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31637347..31637492 26863196 MeRIP-seq:(Medium) rs959630414 Functional Loss SNV dbSNP153 33..33 33 - - - 75510 RMVar_ID_75510 Human_SNP_ID_271999546 m1A Human chr6 + 31637429 31637429 31637429 CGCTGACCTCTCACTGTGACTCACTGTTTAACACATGCCTGTCCCCTAGGCCTCCCCACCAGATG CGCTGACCTCTCACTGTGACTCACTGTTTAACGCATGCCTGTCCCCTAGGCCTCCCCACCAGATG A G PRRC2A Ensembl:ENSG00000204469 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31637426..31637475 32194978 MeRIP-seq:(Medium) rs745879861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1395118,Human_RBP_ID_1671013,Human_RBP_ID_3003238,Human_RBP_ID_3806278,Human_RBP_ID_8642205,Human_RBP_ID_17419654 75511 RMVar_ID_75511 Human_SNP_ID_271999585 m1A Human chr6 + 31637496 31637496 31637496 CTGCGCTGGATACCTAAGCCTTGGGAGCGGACAGGGCCGCCACCTCGAGAAGGGCCCTCCCGACG CTGCGCTGGATACCTAAGCCTTGGGAGCGGACGGGGCCGCCACCTCGAGAAGGGCCCTCCCGACG A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:31637412..31637557;chr6:31637340..31637500 26863196 MeRIP-seq:(Medium) rs1320604504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3806279,Human_RBP_ID_5121892,Human_RBP_ID_8642207,Human_RBP_ID_8900206,Human_RBP_ID_21902305,Human_RBP_ID_26828209 Human_Splice_Rec_752506,Human_Splice_Rec_752566,Human_Splice_Rec_752618 75512 RMVar_ID_75512 Human_SNP_ID_272000223 m1A Human chr6 - 31639198 31639198 31639198 TTAGCTCCGGTCTGATATACAAAAACGACTGCAGGAAGACCCCAACTACAGTCCCCAGCGCTTCC TTAGCTCCGGTCTGATATACAAAAACGACTGCTGGAAGACCCCAACTACAGTCCCCAGCGCTTCC T A BAG6 Ensembl:ENSG00000204463 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31639110..31639246;chr6:31639150..31639235 26863196 MeRIP-seq:(Medium) rs1292703823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661553,Human_RBP_ID_1046865,Human_RBP_ID_2018596,Human_RBP_ID_5617783,Human_RBP_ID_17663954,Human_RBP_ID_18370208 Human_Splice_Rec_752620,Human_Splice_Rec_752626,Human_Splice_Rec_752632,Human_Splice_Rec_752642,Human_Splice_Rec_752690,Human_Splice_Rec_752738,Human_Splice_Rec_752784,Human_Splice_Rec_752830,Human_Splice_Rec_752874 75513 RMVar_ID_75513 Human_SNP_ID_272000660 m1A Human chr6 - 31640436 31640436 31640436 CCTCCTGCTCCTGAGGGGGGCTCCCGGGATGAACAGGATGGAGCTTCAGCTGAGACAGAACCTTG CCTCCTGCTCCTGAGGGGGGCTCCCGGGATGAGCAGGATGGAGCTTCAGCTGAGACAGAACCTTG T C BAG6 Ensembl:ENSG00000204463 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31640376..31640973 32194978 MeRIP-seq:(Medium) rs1195220483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661560,Human_RBP_ID_3806288,Human_RBP_ID_8642218,Human_RBP_ID_8900210,Human_RBP_ID_15786737,Human_RBP_ID_17663609,Human_RBP_ID_22461077 Human_Splice_Rec_752621,Human_Splice_Rec_752638,Human_Splice_Rec_752639,Human_Splice_Rec_752684,Human_Splice_Rec_752685,Human_Splice_Rec_752732,Human_Splice_Rec_752733,Human_Splice_Rec_752778,Human_Splice_Rec_752779,Human_Splice_Rec_752826,Human_Splice_Rec_752827 75514 RMVar_ID_75514 Human_SNP_ID_272000802 m1A Human chr6 - 31640879 31640879 31640879 TCCTTGGTGAGCTGGCTGACCACTATGATGGGACTGAGGCTTCAGGTGGTACTGGAGCACATGCC TCCTTGGTGAGCTGGCTGACCACTATGATGGGGCTGAGGCTTCAGGTGGTACTGGAGCACATGCC T C BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31640744..31640935 26863196 MeRIP-seq:(Medium) rs1416425670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661565,Human_RBP_ID_1671025,Human_RBP_ID_2018600,Human_RBP_ID_3806289,Human_RBP_ID_7592639,Human_RBP_ID_8642220,Human_RBP_ID_8900213,Human_RBP_ID_9262963,Human_RBP_ID_15786744,Human_RBP_ID_18863002,Human_RBP_ID_19016634,Human_RBP_ID_22460585,Human_RBP_ID_22773405,Human_RBP_ID_23214739 Human_Splice_Rec_752627,Human_Splice_Rec_752634,Human_Splice_Rec_752635,Human_Splice_Rec_752680,Human_Splice_Rec_752681,Human_Splice_Rec_752728,Human_Splice_Rec_752729,Human_Splice_Rec_752774,Human_Splice_Rec_752775,Human_Splice_Rec_752822,Human_Splice_Rec_752823,Human_Splice_Rec_752868,Human_Splice_Rec_752869 75515 RMVar_ID_75515 Human_SNP_ID_272002116 m1A Human chr6 - 31645043 31645043 31645043 GTCGAGTCCTCAGCTGAGGGGGCTCCCCCGCCAGGTCCAGCTCCCCCGCCAGCCACCAGCCACCC GTCGAGTCCTCAGCTGAGGGGGCTCCCCCGCCCGGTCCAGCTCCCCCGCCAGCCACCAGCCACCC T G BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31645026..31645050 26863196 MeRIP-seq:(Medium) rs755691531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252583,Human_RBP_ID_792340,Human_RBP_ID_18073683,Human_RBP_ID_18195444,Human_RBP_ID_22311156,Human_RBP_ID_22534178,Human_RBP_ID_22831294 Human_Splice_Rec_752661,Human_Splice_Rec_752709,Human_Splice_Rec_752755,Human_Splice_Rec_752803,Human_Splice_Rec_752849,Human_Splice_Rec_752905,Human_Splice_Rec_752921,Human_Splice_Rec_752931,Human_Splice_Rec_752937,Human_Splice_Rec_752961,Human_Splice_Rec_752965 75516 RMVar_ID_75516 Human_SNP_ID_272002123 m1A Human chr6 + 31645052 31645052 31645052 GTGGCTGGCGGGGGAGCTGGACCTGGCGGGGGAGCCCCCTCAGCTGAGGACTCGACATTGGTAGA GTGGCTGGCGGGGGAGCTGGACCTGGCGGGGGGGCCCCCTCAGCTGAGGACTCGACATTGGTAGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr6:31645001..31645150;chr6:31645002..31645140 26863196 MeRIP-seq:(Medium) rs922860190 Functional Loss SNV dbSNP153 33..33 33 - - - 75517 RMVar_ID_75517 Human_SNP_ID_272002245 m1A Human chr6 - 31645448 31645448 31645448 ACCTGCATGTGGTCCGGCCTATGTCTCACTACACCACCCCCATGGTGCTCCAGCAGGCAGCCATT ACCTGCATGTGGTCCGGCCTATGTCTCACTACTCCACCCCCATGGTGCTCCAGCAGGCAGCCATT T A BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31645401..31645500 26863196 MeRIP-seq:(Medium) rs1413386506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046880,Human_RBP_ID_1326901,Human_RBP_ID_4881654,Human_RBP_ID_8642236,Human_RBP_ID_9308261,Human_RBP_ID_17306569,Human_RBP_ID_17419665,Human_RBP_ID_18195446,Human_RBP_ID_18863016,Human_RBP_ID_24157140,Human_RBP_ID_27523421 Human_Splice_Rec_752659,Human_Splice_Rec_752707,Human_Splice_Rec_752753,Human_Splice_Rec_752801,Human_Splice_Rec_752847,Human_Splice_Rec_752903,Human_Splice_Rec_752929,Human_Splice_Rec_752935,Human_Splice_Rec_752959 75518 RMVar_ID_75518 Human_SNP_ID_272002465 m1A Human chr6 - 31646360 31646360 31646360 TGAGCCCTTTGATGGCCCTGCCCTTTCTCCTCAGCCCCAGTACTCCCAAAACAGAACAGGCTGAA TGAGCCCTTTGATGGCCCTGCCCTTTCTCCTCGGCCCCAGTACTCCCAAAACAGAACAGGCTGAA T C BAG6 Ensembl:ENSG00000204463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31646355..31646554 26863196 MeRIP-seq:(Medium) rs1464331187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19128878,Human_RBP_ID_24387659 75519 RMVar_ID_75519 Human_SNP_ID_272002900 m1A Human chr6 + 31647696 31647696 31647696 CTGGGGCACGCTCCTCCACTTCTTCTGCCTCCATGGGCTCCCGGGGAGGTGCTTCACTTTCAACT CTGGGGCACGCTCCTCCACTTCTTCTGCCTCCGTGGGCTCCCGGGGAGGTGCTTCACTTTCAACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31647645..31647850 26863196 MeRIP-seq:(Medium) rs1396958159 Functional Loss SNV dbSNP153 33..33 33 - - - 75520 RMVar_ID_75520 Human_SNP_ID_272004067 m1A Human chr6 - 31651759 31651759 31651759 TTCGTTCTTCTTTAGAGACCTGTCGGCCATGGAGCCTAATGATAGTACCAGTACCGCTGTGGAGG TTCGTTCTTCTTTAGAGACCTGTCGGCCATGGGGCCTAATGATAGTACCAGTACCGCTGTGGAGG T C BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31651661..31651810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_661591,Human_RBP_ID_2018624,Human_RBP_ID_3968750,Human_RBP_ID_4911841,Human_RBP_ID_8900250,Human_RBP_ID_15786862,Human_RBP_ID_18073695,Human_RBP_ID_18195738 Human_Splice_Rec_752644,Human_Splice_Rec_752692,Human_Splice_Rec_752740,Human_Splice_Rec_752786,Human_Splice_Rec_752832,Human_Splice_Rec_752888,Human_Splice_Rec_752944,Human_Splice_Rec_752968,Human_Splice_Rec_752978,Human_Splice_Rec_752990,Human_Splice_Rec_753000,Human_Splice_Rec_753012,Human_Splice_Rec_753022,Human_Splice_Rec_753034,Human_Splice_Rec_753046,Human_Splice_Rec_753056,Human_Splice_Rec_753076 75521 RMVar_ID_75521 Human_SNP_ID_272006052 m1A Human chr6 + 31659032 31659032 31659032 GTCATGCCTCACACTTTTCTCCTAAAGCCCACACTCTCTTCACCCTTTGCCCCCACCCCACGGTC GTCATGCCTCACACTTTTCTCCTAAAGCCCACGCTCTCTTCACCCTTTGCCCCCACCCCACGGTC A G C6orf47-AS1 Ensembl:ENSG00000227198 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31658880..31659187 26863196 MeRIP-seq:(Medium) rs375479061 Functional Loss SNV dbSNP153 33..33 33 - - - 75522 RMVar_ID_75522 Human_SNP_ID_272006225 m1A Human chr6 - 31659459 31659459 31659459 AAGCTGTTGGGCTGGCTGCGGGGGGAACCAGGAGCTCCCTCCCGGTACTTGGGGGGCCCAGAAGA AAGCTGTTGGGCTGGCTGCGGGGGGAACCAGGTGCTCCCTCCCGGTACTTGGGGGGCCCAGAAGA T A C6orf47 Ensembl:ENSG00000204439 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31659188..31659683 32194978 MeRIP-seq:(Medium) rs1180563133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5428410,Human_RBP_ID_7662440,Human_RBP_ID_9309622,Human_RBP_ID_17042049,Human_RBP_ID_27345646,Human_RBP_ID_27523438 75523 RMVar_ID_75523 Human_SNP_ID_272006317 m1A Human chr6 - 31659725 31659725 31659725 TGAGGGTTTCTGGGGCTGCTTCCGAACCAAGCAAGGAGGAGCCCCAAGTTGAGCAGCTAGGGAGC TGAGGGTTTCTGGGGCTGCTTCCGAACCAAGCGAGGAGGAGCCCCAAGTTGAGCAGCTAGGGAGC T C C6orf47 Ensembl:ENSG00000204439 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31659676..31659758 26863196 MeRIP-seq:(Medium) rs1183708431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22106748,Human_RBP_ID_27345649 75524 RMVar_ID_75524 Human_SNP_ID_272007575 m1A Human chr6 - 31663943 31663943 31663943 CTGGGTGGGGGTCTGTGAGCTGAGTGGCAGGGATGCGGCTCAGCTCGCTGAAGAAGCTGGCTTCC CTGGGTGGGGGTCTGTGAGCTGAGTGGCAGGGGTGCGGCTCAGCTCGCTGAAGAAGCTGGCTTCC T C GPANK1 Ensembl:ENSG00000204438 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31663895..31663975 26863196 MeRIP-seq:(Medium) rs201945052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251891,Human_RBP_ID_791340,Human_RBP_ID_949253,Human_RBP_ID_5327096,Human_RBP_ID_5399395,Human_RBP_ID_5478523,Human_RBP_ID_19016642,Human_RBP_ID_22104870,Human_RBP_ID_22728142,Human_RBP_ID_26353648,Human_RBP_ID_26792942 Human_Splice_Rec_753115,Human_Splice_Rec_753121,Human_Splice_Rec_753127,Human_Splice_Rec_753133,Human_Splice_Rec_753139 75525 RMVar_ID_75525 Human_SNP_ID_272008355 m1A Human chr6 + 31666139 31666139 31666139 CCTGCCGCGGTCGGGTCCGCGGCCTGCGCTGTAGCGGTCGCCGCCGTTCCCTGGAAGTAGCAACT CCTGCCGCGGTCGGGTCCGCGGCCTGCGCTGTGGCGGTCGCCGCCGTTCCCTGGAAGTAGCAACT A G CSNK2B,AL662899.4 Ensembl:ENSG00000204435,Ensembl:ENSG00000263020 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31666076..31666925;chr6:31666101..31666188;chr6:31666034..31667990;chr6:31666076..31667924 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs889024432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252561,Human_RBP_ID_661608,Human_RBP_ID_791332,Human_RBP_ID_4881852,Human_RBP_ID_5511441,Human_RBP_ID_17421552,Human_RBP_ID_18958144 Human_Splice_Rec_753165,Human_Splice_Rec_753177,Human_Splice_Rec_753185,Human_Splice_Rec_753189,Human_Splice_Rec_753197,Human_Splice_Rec_753223 75526 RMVar_ID_75526 Human_SNP_ID_272008369 m1A Human chr6 - 31666176 31666176 31666176 CGGCTGGACGGGGACCAGGACTGGGGTGGGGTAGGGAAGTTGCTACTTCCAGGGAACGGCGGCGA CGGCTGGACGGGGACCAGGACTGGGGTGGGGTGGGGAAGTTGCTACTTCCAGGGAACGGCGGCGA T C GPANK1 Ensembl:ENSG00000204438 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31666076..31667875 26863410 MeRIP-seq:(Medium) rs567067253 Functional Loss SNV dbSNP153 33..33 33 - - - 75527 RMVar_ID_75527 Human_SNP_ID_272009097 m1A Human chr6 + 31668635 31668635 31668635 TGGATTGATCCACGCCCGCTACATCCTTACCAACCGTGGCATCGCCCAGATGGTGAGGCCTCTCT TGGATTGATCCACGCCCGCTACATCCTTACCACCCGTGGCATCGCCCAGATGGTGAGGCCTCTCT A C CSNK2B,AL662899.4 Ensembl:ENSG00000204435,Ensembl:ENSG00000263020 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31668586..31668678 26863196 MeRIP-seq:(Medium) rs756658867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791338,Human_RBP_ID_9308262,Human_RBP_ID_9400270,Human_RBP_ID_17306585,Human_RBP_ID_18171073,Human_RBP_ID_18472048,Human_RBP_ID_18863060,Human_RBP_ID_19018065,Human_RBP_ID_19128890,Human_RBP_ID_26828231 Human_Splice_Rec_753158,Human_Splice_Rec_753159,Human_Splice_Rec_753170,Human_Splice_Rec_753171,Human_Splice_Rec_753182,Human_Splice_Rec_753194,Human_Splice_Rec_753195,Human_Splice_Rec_753204,Human_Splice_Rec_753205,Human_Splice_Rec_753216,Human_Splice_Rec_753217,Human_Splice_Rec_753228,Human_Splice_Rec_753229,Human_Splice_Rec_753240,Human_Splice_Rec_753241 RMVar_hsa_circ_17362 75528 RMVar_ID_75528 Human_SNP_ID_272010287 m1A Human chr6 + 31672682 31672682 31672682 TGGTCAGGCTGGTCTCGAACTCCTGACCTCGTAATCTGCCCTCCTCGACCTCCCAAAGTGCCGGG TGGTCAGGCTGGTCTCGAACTCCTGACCTCGTGATCTGCCCTCCTCGACCTCCCAAAGTGCCGGG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1405452133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23195151 75529 RMVar_ID_75529 Human_SNP_ID_272010386 m1A Human chr6 + 31673087 31673087 31673087 TGGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAACCCGCTCTCTATTAAAAATAGAAAAATCA TGGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCGCTCTCTATTAAAAATAGAAAAATCA A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1365873945 Functional Loss SNV dbSNP153 33..33 33 - - - 75530 RMVar_ID_75530 Human_SNP_ID_272013666 m1A Human chr6 - 31687096 31687096 31687096 TGTTGCTGTTTATAGTTTGTGGAAAGTGGGGGACCATCCCCCTTCTCACCACTGTTCCTCTTGCA TGTTGCTGTTTATAGTTTGTGGAAAGTGGGGGGCCATCCCCCTTCTCACCACTGTTCCTCTTGCA T C ABHD16A,AL662899.3 Ensembl:ENSG00000204427,Ensembl:ENSG00000204422 Protein coding,Protein coding exon,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31687047..31687275 32194978 MeRIP-seq:(Medium) rs970257900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791324,Human_RBP_ID_5121898,Human_RBP_ID_17663111,Human_RBP_ID_18863094,Human_RBP_ID_21902309,Human_RBP_ID_23214743 75531 RMVar_ID_75531 Human_SNP_ID_272023821 m1A Human chr6 - 31728627 31728627 31728627 CGTTCTCTTCACCGGTGAGGCTGGGGGGAGGCATAGGTCTTGGCACAGGGAAGTAGAGTTTGGGA CGTTCTCTTCACCGGTGAGGCTGGGGGGAGGCGTAGGTCTTGGCACAGGGAAGTAGAGTTTGGGA T C DDAH2 Ensembl:ENSG00000213722 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31728626..31729070 32194978 MeRIP-seq:(Medium) rs367611448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1326913,Human_RBP_ID_5268528,Human_RBP_ID_5398040,Human_RBP_ID_19128914 75532 RMVar_ID_75532 Human_SNP_ID_272025094 m1A Human chr6 - 31733931 31733930 31733931 AGGCGGACCGAGACAGTGCAGAAGCTGTGCCCAGGGGGGCAGCTCCCATTCCTGCTGTATGGCAC AGGCGGACCGAGACAGTGCAGAAGCTGTGCCC_GGGGGGCAGCTCCCATTCCTGCTGTATGGCAC CT C CLIC1 Ensembl:ENSG00000213719 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31733799..31734007 26863196 MeRIP-seq:(Medium) rs773911287 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_172886,Human_RBP_ID_252712,Human_RBP_ID_791466,Human_RBP_ID_5122393,Human_RBP_ID_8905248,Human_RBP_ID_9193545,Human_RBP_ID_18195465,Human_RBP_ID_22460597,Human_RBP_ID_22683884,Human_RBP_ID_26829409 Human_Splice_Rec_753836,Human_Splice_Rec_753837,Human_Splice_Rec_753848,Human_Splice_Rec_753849,Human_Splice_Rec_753860,Human_Splice_Rec_753861,Human_Splice_Rec_753874,Human_Splice_Rec_753875,Human_Splice_Rec_753886,Human_Splice_Rec_753887 RMVar_hsa_circ_68412 75533 RMVar_ID_75533 Human_SNP_ID_272025191 m1A Human chr6 + 31734261 31734261 31734261 GGGCAGTTCCCAATCTTGGCCCCATCACTGCCAGCCTGAAAAGTAACCCCAACCCAAGGTTATGC GGGCAGTTCCCAATCTTGGCCCCATCACTGCCGGCCTGAAAAGTAACCCCAACCCAAGGTTATGC A G RF00017-4498,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31734105..31734310 26863196 MeRIP-seq:(Medium) rs1449105481 Functional Loss SNV dbSNP153 33..33 33 - - - 75534 RMVar_ID_75534 Human_SNP_ID_272025467 m1A Human chr6 - 31735510 31735510 31735510 AGGGCATTTTGGGATTTGGGGGTTGGAGAAGTAGAAGACTTGCCCCAACTCTCTCCTCTCTCTGC AGGGCATTTTGGGATTTGGGGGTTGGAGAAGTCGAAGACTTGCCCCAACTCTCTCCTCTCTCTGC T G CLIC1 Ensembl:ENSG00000213719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31735507..31735800 26863196 MeRIP-seq:(Medium) rs558065714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956,Human_RBP_ID_3822111,Human_RBP_ID_5304242,Human_RBP_ID_5400432,Human_RBP_ID_5656270,Human_RBP_ID_9437398,Human_RBP_ID_24157297 RMVar_hsa_circ_68412 75535 RMVar_ID_75535 Human_SNP_ID_272025701 m1A Human chr6 - 31736333 31736333 31736333 CTTCCCCGGTCCCAGCCCCTCCCAGTTCCCCCAGGGACGGCCACTTCCTGGTCCCCGACGCAACC CTTCCCCGGTCCCAGCCCCTCCCAGTTCCCCCGGGGACGGCCACTTCCTGGTCCCCGACGCAACC T C CLIC1 Ensembl:ENSG00000213719 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31736287..31736475 26863196 MeRIP-seq:(Medium) rs767435569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252713,Human_RBP_ID_661690,Human_RBP_ID_791468,Human_RBP_ID_1046909,Human_RBP_ID_4903200,Human_RBP_ID_5327102,Human_RBP_ID_5428419,Human_RBP_ID_5451105,Human_RBP_ID_5478047,Human_RBP_ID_5511446,Human_RBP_ID_9336057,Human_RBP_ID_22461096,Human_RBP_ID_24157306,Human_RBP_ID_26535402,Human_RBP_ID_27096200,Human_RBP_ID_27523497 Human_Splice_Rec_753833,Human_Splice_Rec_753844,Human_Splice_Rec_753845,Human_Splice_Rec_753856,Human_Splice_Rec_753857,Human_Splice_Rec_753870,Human_Splice_Rec_753871,Human_Splice_Rec_753882,Human_Splice_Rec_753883 RMVar_hsa_circ_68412 75536 RMVar_ID_75536 Human_SNP_ID_272025702 m1A Human chr6 - 31736333 31736333 31736333 CTTCCCCGGTCCCAGCCCCTCCCAGTTCCCCCAGGGACGGCCACTTCCTGGTCCCCGACGCAACC CTTCCCCGGTCCCAGCCCCTCCCAGTTCCCCCCGGGACGGCCACTTCCTGGTCCCCGACGCAACC T G CLIC1 Ensembl:ENSG00000213719 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31736287..31736475 26863196 MeRIP-seq:(Medium) rs767435569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252713,Human_RBP_ID_661690,Human_RBP_ID_791468,Human_RBP_ID_1046909,Human_RBP_ID_4903200,Human_RBP_ID_5327102,Human_RBP_ID_5428419,Human_RBP_ID_5451105,Human_RBP_ID_5478047,Human_RBP_ID_5511446,Human_RBP_ID_9336057,Human_RBP_ID_22461096,Human_RBP_ID_24157306,Human_RBP_ID_26535402,Human_RBP_ID_27096200,Human_RBP_ID_27523497 Human_Splice_Rec_753833,Human_Splice_Rec_753844,Human_Splice_Rec_753845,Human_Splice_Rec_753856,Human_Splice_Rec_753857,Human_Splice_Rec_753870,Human_Splice_Rec_753871,Human_Splice_Rec_753882,Human_Splice_Rec_753883 RMVar_hsa_circ_68412 75537 RMVar_ID_75537 Human_SNP_ID_272025705 m1A Human chr6 + 31736340 31736340 31736340 TCGGGGACCAGGAAGTGGCCGTCCCTGGGGGAACTGGGAGGGGCTGGGACCGGGGAAGGCGGGTC TCGGGGACCAGGAAGTGGCCGTCCCTGGGGGAGCTGGGAGGGGCTGGGACCGGGGAAGGCGGGTC A G RF00017-4498,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31736297..31736525 26863196 MeRIP-seq:(Medium) rs1467249972 Functional Loss SNV dbSNP153 33..33 33 - - - 75538 RMVar_ID_75538 Human_SNP_ID_272026641 m1A Human chr6 - 31740087 31740087 31740087 TATCTTCCTCCTCCCCCAGCTGCCGCCATCGCAGCGTTTTCCCGCCTTTTCAGTAACCTGAGTCG TATCTTCCTCCTCCCCCAGCTGCCGCCATCGCTGCGTTTTCCCGCCTTTTCAGTAACCTGAGTCG T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31740038..31740178;chr6:31740047..31740197;chr6:31740051..31740154 26863196 MeRIP-seq:(Medium) rs1047802550 Functional Loss SNV dbSNP153 33..33 33 - - - 75539 RMVar_ID_75539 Human_SNP_ID_272032618 m1A Human chr6 - 31762925 31762925 31762925 CCTCTCAGGCCCCTTCCTGCTGTGTCTGTCTGAGGCTGGGGTGTTCCTACTTGAGAAGAGAGACC CCTCTCAGGCCCCTTCCTGCTGTGTCTGTCTGCGGCTGGGGTGTTCCTACTTGAGAAGAGAGACC T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31762877..31762958 26863196 MeRIP-seq:(Medium) rs1408630936 Functional Loss SNV dbSNP153 33..33 33 - - - 75540 RMVar_ID_75540 Human_SNP_ID_272037656 m1A Human chr6 - 31780101 31780099 31780101 GGTGGACCGCTGGATCCGCAGCCGCCTGACAGAGGCTGTGAGGCTCAGCAATCAAGGCTTCCAGG GGTGGACCGCTGGATCCGCAGCCGCCTGACAG__GCTGTGAGGCTCAGCAATCAAGGCTTCCAGG CCT C VARS1 Ensembl:ENSG00000204394 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31780051..31780125 32194978 MeRIP-seq:(Medium) rs778683620 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8900275 Human_Splice_Rec_754608 Human_miRNA_ID_2208633,Human_miRNA_ID_3033240 RMVar_hsa_circ_91329,RMVar_hsa_circ_237829 75541 RMVar_ID_75541 Human_SNP_ID_272038257 m1A Human chr6 + 31781926 31781926 31781926 GCCTTCTCCCGGGCCTCCGCCTCATTGCGTCCACTCACCCAGTACCGCCCATCAGGGTCCTGCCA GCCTTCTCCCGGGCCTCCGCCTCATTGCGTCCCCTCACCCAGTACCGCCCATCAGGGTCCTGCCA A C RF00017-4498,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr6:31781857..31781966;chr6:31781876..31781950 26863196,32194978 MeRIP-seq:(Medium) rs867991903 Functional Loss SNV dbSNP153 33..33 33 - - - 75542 RMVar_ID_75542 Human_SNP_ID_272040765 m1A Human chr6 + 31791970 31791970 31791970 GGGCTGTAGGAGTCGGGCATGGGGCCACTGACATCTGGGGGAGAGGAAGGGAGGGCTCAGTGCCG GGGCTGTAGGAGTCGGGCATGGGGCCACTGACCTCTGGGGGAGAGGAAGGGAGGGCTCAGTGCCG A C RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31791851..31791975 32194978 MeRIP-seq:(Medium) rs1453026753 Functional Loss SNV dbSNP153 33..33 33 - - - 75543 RMVar_ID_75543 Human_SNP_ID_272041670 m1A Human chr6 + 31795214 31795214 31795214 GGCATCTGGGTGAGGGGAGACGTAGAGGGTGGACATAGTTATGAGAAGGTCCGAACGAAGTGGAA GGCATCTGGGTGAGGGGAGACGTAGAGGGTGGGCATAGTTATGAGAAGGTCCGAACGAAGTGGAA A G RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31795051..31795299 26863196 MeRIP-seq:(Medium) rs770966756 Functional Loss SNV dbSNP153 33..33 33 - - - 75544 RMVar_ID_75544 Human_SNP_ID_272041671 m1A Human chr6 + 31795214 31795214 31795214 GGCATCTGGGTGAGGGGAGACGTAGAGGGTGGACATAGTTATGAGAAGGTCCGAACGAAGTGGAA GGCATCTGGGTGAGGGGAGACGTAGAGGGTGGTCATAGTTATGAGAAGGTCCGAACGAAGTGGAA A T RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31795051..31795299 26863196 MeRIP-seq:(Medium) rs770966756 Functional Loss SNV dbSNP153 33..33 33 - - - 75545 RMVar_ID_75545 Human_SNP_ID_272041674 m1A Human chr6 - 31795217 31795217 31795217 TTTTTCCACTTCGTTCGGACCTTCTCATAACTATGTCCACCCTCTACGTCTCCCCTCACCCAGAT TTTTTCCACTTCGTTCGGACCTTCTCATAACTGTGTCCACCCTCTACGTCTCCCCTCACCCAGAT T C VARS1 Ensembl:ENSG00000204394 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31795076..31795325 26863196 MeRIP-seq:(Medium) rs1278900862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671193,Human_RBP_ID_3806398,Human_RBP_ID_5428423,Human_RBP_ID_17306600,Human_RBP_ID_17535654,Human_RBP_ID_21325328,Human_RBP_ID_25997541,Human_RBP_ID_27096271 Human_Splice_Rec_754562 75546 RMVar_ID_75546 Human_SNP_ID_272041789 m1A Human chr6 - 31795680 31795680 31795680 GGGCGCCGGCTGCCGGGGCGGCGATCTTAGGGAACTAGGGTCACCTGGAGAGCCGCCCACCGTCT GGGCGCCGGCTGCCGGGGCGGCGATCTTAGGGCACTAGGGTCACCTGGAGAGCCGCCCACCGTCT T G VARS1 Ensembl:ENSG00000204394 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:31795469..31795815;chr6:31795480..31795750 26863196 MeRIP-seq:(Medium) rs964312692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661720,Human_RBP_ID_4903206,Human_RBP_ID_9309239 75547 RMVar_ID_75547 Human_SNP_ID_272044552 m1A Human chr6 - 31806847 31806837 31806848 CCCGCTGCGCCTGCGCGGTCCCGCCTCGCCCCACGCGCGGGCTCGCGCTTCGGTTTCCCCAGACC CCCGCTGCGCCTGCGCGGTCCCGCCTCGCCC___________TCGCGCTTCGGTTTCCCCAGACC AGCCCGCGCGTG A LSM2 Ensembl:ENSG00000204392 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31806801..31806975 26863196 MeRIP-seq:(Medium) rs908819959 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_661745,Human_RBP_ID_791295,Human_RBP_ID_4882276,Human_RBP_ID_5327106,Human_RBP_ID_17421554,Human_RBP_ID_22461889 Human_Splice_Rec_754713,Human_Splice_Rec_754719,Human_Splice_Rec_754725,Human_Splice_Rec_754729 75548 RMVar_ID_75548 Human_SNP_ID_272047220 m1A Human chr6 - 31815602 31815602 31815602 CGCACAGGTTCGCTCTGGGAAGCCTTGGGACAACGGGAGTCACTCTCGAAAAAGGTAGTGGACTG CGCACAGGTTCGCTCTGGGAAGCCTTGGGACAGCGGGAGTCACTCTCGAAAAAGGTAGTGGACTG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31815551..31815762;chr6:31815543..31815777 26863196 MeRIP-seq:(Medium) rs1178863029 Functional Loss SNV dbSNP153 33..33 33 - - - 75549 RMVar_ID_75549 Human_SNP_ID_272047268 m1A Human chr6 - 31815703 31815701 31815703 GGCTCCGCTCTGAGATTGGGGGCTGGAAACGGAACACTGGATCCGCGAGAAGAGCTCGGTCCTTC GGCTCCGCTCTGAGATTGGGGGCTGGAAACGG__CACTGGATCCGCGAGAAGAGCTCGGTCCTTC GTT G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31815551..31815724 26863196 MeRIP-seq:(Medium) rs1259315869 Functional Loss DEL dbSNP153 33..34 33 - - - 75550 RMVar_ID_75550 Human_SNP_ID_272047268 m1A Human chr6 - 31815702 31815701 31815703 GCTCCGCTCTGAGATTGGGGGCTGGAAACGGAACACTGGATCCGCGAGAAGAGCTCGGTCCTTCC GCTCCGCTCTGAGATTGGGGGCTGGAAACGG__CACTGGATCCGCGAGAAGAGCTCGGTCCTTCC GTT G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31815651..31815725 26863196 MeRIP-seq:(Medium) rs1259315869 Functional Loss DEL dbSNP153 32..33 33 - - - 75551 RMVar_ID_75551 Human_SNP_ID_272047269 m1A Human chr6 - 31815702 31815702 31815702 GCTCCGCTCTGAGATTGGGGGCTGGAAACGGAACACTGGATCCGCGAGAAGAGCTCGGTCCTTCC GCTCCGCTCTGAGATTGGGGGCTGGAAACGGAGCACTGGATCCGCGAGAAGAGCTCGGTCCTTCC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31815651..31815725 26863196 MeRIP-seq:(Medium) rs894889216 Functional Loss SNV dbSNP153 33..33 33 - - - 75552 RMVar_ID_75552 Human_SNP_ID_272047270 m1A Human chr6 - 31815703 31815703 31815703 GGCTCCGCTCTGAGATTGGGGGCTGGAAACGGAACACTGGATCCGCGAGAAGAGCTCGGTCCTTC GGCTCCGCTCTGAGATTGGGGGCTGGAAACGGCACACTGGATCCGCGAGAAGAGCTCGGTCCTTC T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31815551..31815724 26863196 MeRIP-seq:(Medium) rs1013380778 Functional Loss SNV dbSNP153 33..33 33 - - - 75553 RMVar_ID_75553 Human_SNP_ID_272047683 m1A Human chr6 + 31817462 31817462 31817462 CAAGGGCAAGATCAGCGAGGCGGACAAGAAGAAGGTGCTGGACAAGTGTCAAGAGGTCATCTCGT CAAGGGCAAGATCAGCGAGGCGGACAAGAAGATGGTGCTGGACAAGTGTCAAGAGGTCATCTCGT A T HSPA1A Ensembl:ENSG00000204389 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31817422..31817517 26863196 MeRIP-seq:(Medium) rs781009367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7592976,Human_RBP_ID_18413843,Human_RBP_ID_18539069,Human_RBP_ID_22105801,Human_RBP_ID_23067527,Human_RBP_ID_23116423,Human_RBP_ID_23314643,Human_RBP_ID_24548375,Human_RBP_ID_26353688 75554 RMVar_ID_75554 Human_SNP_ID_272048898 m1A Human chr6 + 31822210 31822210 31822210 GAAGTTTCTAGAGTTTTCTGACCTTCAAGGCGAGAACTGCTGTGTCATTCTTAGGGACACTCCCC GAAGTTTCTAGAGTTTTCTGACCTTCAAGGCGGGAACTGCTGTGTCATTCTTAGGGACACTCCCC A G lnc-HSPA1B-1,RF00017-4501 RNACentral:URS0000E24BC4,RNACentral:URS0000972B66 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31822208..31822285 26863196 MeRIP-seq:(Medium) rs113384835 Functional Loss SNV dbSNP153 33..33 33 - - - 75555 RMVar_ID_75555 Human_SNP_ID_272050247 m1A Human chr6 - 31827793 31827793 31827793 AGGTTCGCTCTGGAAAGCCTTGGGACCGCGGGAGTCACTCTCGAAAGACGAAGCGGACCCTCGCA AGGTTCGCTCTGGAAAGCCTTGGGACCGCGGGTGTCACTCTCGAAAGACGAAGCGGACCCTCGCA T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:31827726..31827986;chr6:31827726..31828000;chr6:31827726..31827984 26863196 MeRIP-seq:(Medium) rs751251143 Functional Loss SNV dbSNP153 33..33 33 - - - 75556 RMVar_ID_75556 Human_SNP_ID_272050265 m1A Human chr6 + 31827822 31827822 31827822 GACTCCCGCGGTCCCAAGGCTTTCCAGAGCGAACCTGTGCGGCTGCAGGCACCGGCGTGTTGAGT GACTCCCGCGGTCCCAAGGCTTTCCAGAGCGAGCCTGTGCGGCTGCAGGCACCGGCGTGTTGAGT A G HSPA1B Ensembl:ENSG00000204388 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31827799..31827932 26863196 MeRIP-seq:(Medium) rs1272020678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661750,Human_RBP_ID_1217267,Human_RBP_ID_2018748,Human_RBP_ID_3806411,Human_RBP_ID_4903208,Human_RBP_ID_5478690,Human_RBP_ID_5533041,Human_RBP_ID_7592997,Human_RBP_ID_8642383,Human_RBP_ID_8905757,Human_RBP_ID_9309243,Human_RBP_ID_9336068,Human_RBP_ID_18863175,Human_RBP_ID_22104899,Human_RBP_ID_22461109,Human_RBP_ID_26535416,Human_RBP_ID_27096289,Human_RBP_ID_27345755 75557 RMVar_ID_75557 Human_SNP_ID_272050281 m1A Human chr6 - 31827847 31827847 31827847 AGCTCAGTCCTTCGGAACGCCGGAAACTCAACACGCCGGTGCCTGCAGCCGCACAGGTTCGCTCT AGCTCAGTCCTTCGGAACGCCGGAAACTCAACGCGCCGGTGCCTGCAGCCGCACAGGTTCGCTCT T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr6:31827769..31827919;chr6:31827751..31828000 26863196,32194978 MeRIP-seq:(Medium) rs2607020 Functional Loss SNV dbSNP153 33..33 33 - - - 75558 RMVar_ID_75558 Human_SNP_ID_272050300 m1A Human chr6 - 31827874 31827874 31827874 GAAACGGCGGACGGGATCCGCGACAAGAGCTCAGTCCTTCGGAACGCCGGAAACTCAACACGCCG GAAACGGCGGACGGGATCCGCGACAAGAGCTCGGTCCTTCGGAACGCCGGAAACTCAACACGCCG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31827823..31828000 26863196 MeRIP-seq:(Medium) rs2607018 Functional Loss SNV dbSNP153 33..33 33 - - - 75559 RMVar_ID_75559 Human_SNP_ID_272050301 m1A Human chr6 - 31827874 31827874 31827874 GAAACGGCGGACGGGATCCGCGACAAGAGCTCAGTCCTTCGGAACGCCGGAAACTCAACACGCCG GAAACGGCGGACGGGATCCGCGACAAGAGCTCCGTCCTTCGGAACGCCGGAAACTCAACACGCCG T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31827823..31828000 26863196 MeRIP-seq:(Medium) rs2607018 Functional Loss SNV dbSNP153 33..33 33 - - - 75560 RMVar_ID_75560 Human_SNP_ID_272050304 m1A Human chr6 - 31827879 31827879 31827879 GGCTGGAAACGGCGGACGGGATCCGCGACAAGAGCTCAGTCCTTCGGAACGCCGGAAACTCAACA GGCTGGAAACGGCGGACGGGATCCGCGACAAGGGCTCAGTCCTTCGGAACGCCGGAAACTCAACA T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31827751..31827925 26863196 MeRIP-seq:(Medium) rs1562368284 Functional Loss SNV dbSNP153 33..33 33 - - - 75561 RMVar_ID_75561 Human_SNP_ID_272050586 m1A Human chr6 + 31829229 31829229 31829229 GCAACTCCACCATCCCCACCAAGCAGACGCAGATCTTCACCACCTACTCCGACAACCAACCCGGG GCAACTCCACCATCCCCACCAAGCAGACGCAGTTCTTCACCACCTACTCCGACAACCAACCCGGG A T HSPA1B,AL671762.1 Ensembl:ENSG00000204388,Ensembl:ENSG00000285565 Protein coding,lincRNA CDS,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31829226..31829325 26863196 MeRIP-seq:(Medium) rs1390970619 Functional Loss SNV dbSNP153 33..33 33 - - - 75562 RMVar_ID_75562 Human_SNP_ID_272050719 m1A Human chr6 + 31829656 31829656 31829656 CAAGGGCAAGATCAGCGAGGCGGACAAGAAGAAGGTTCTGGACAAGTGTCAAGAGGTCATCTCGT CAAGGGCAAGATCAGCGAGGCGGACAAGAAGATGGTTCTGGACAAGTGTCAAGAGGTCATCTCGT A T HSPA1B,AL671762.1 Ensembl:ENSG00000204388,Ensembl:ENSG00000285565 Protein coding,lincRNA CDS,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31829601..31829725 26863196 MeRIP-seq:(Medium) rs749173984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1217270,Human_RBP_ID_2018752,Human_RBP_ID_3806413,Human_RBP_ID_4882281,Human_RBP_ID_7593000,Human_RBP_ID_8270119,Human_RBP_ID_8900325,Human_RBP_ID_9400288,Human_RBP_ID_15787933,Human_RBP_ID_18073833,Human_RBP_ID_18171082,Human_RBP_ID_18539070,Human_RBP_ID_18863177,Human_RBP_ID_22311265,Human_RBP_ID_24157403,Human_RBP_ID_24548376,Human_RBP_ID_26353692,Human_RBP_ID_27096292,Human_RBP_ID_27345759,Human_RBP_ID_27523544,Human_RBP_ID_27828430 Human_Splice_Rec_754743 75563 RMVar_ID_75563 Human_SNP_ID_272050722 m1A Human chr6 - 31829660 31829660 31829660 AGCCACGAGATGACCTCTTGACACTTGTCCAGAACCTTCTTCTTGTCCGCCTCGCTGATCTTGCC AGCCACGAGATGACCTCTTGACACTTGTCCAGCACCTTCTTCTTGTCCGCCTCGCTGATCTTGCC T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31829601..31829725 32194978 MeRIP-seq:(Medium) rs35682610 Functional Loss SNV dbSNP153,EGP,HGVD 33..33 33 - - - 75564 RMVar_ID_75564 Human_SNP_ID_272050805 m1A Human chr6 + 31829866 31829866 31829866 GGGAGGGTCTGGGTCAGGCCCTACCATTGAGGAGGTGGATTAGGGGCCTTTGTTCTTTAGTATGT GGGAGGGTCTGGGTCAGGCCCTACCATTGAGGCGGTGGATTAGGGGCCTTTGTTCTTTAGTATGT A C HSPA1B,AL671762.1 Ensembl:ENSG00000204388,Ensembl:ENSG00000285565 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31829801..31829950;chr6:31829601..31829925;chr6:31829732..31829925 26863196 MeRIP-seq:(Medium) rs779265498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13399,Human_RBP_ID_791288,Human_RBP_ID_1217271,Human_RBP_ID_1678483,Human_RBP_ID_2018754,Human_RBP_ID_3806414,Human_RBP_ID_4882284,Human_RBP_ID_5151832,Human_RBP_ID_7593004,Human_RBP_ID_8900327,Human_RBP_ID_9336069,Human_RBP_ID_15787935,Human_RBP_ID_17634026,Human_RBP_ID_18425902,Human_RBP_ID_18465513,Human_RBP_ID_18863179,Human_RBP_ID_22104900,Human_RBP_ID_22461894,Human_RBP_ID_22773418,Human_RBP_ID_24157405,Human_RBP_ID_26771730,Human_RBP_ID_27096294,Human_RBP_ID_27842600 Human_miRNA_ID_209115 75565 RMVar_ID_75565 Human_SNP_ID_272050820 m1A Human chr6 - 31829902 31829897 31829903 AAGTCCTTGAGTCCCAACAGTCCACCTCAAAGACAAACATACTAAAGAACAAAGGCCCCTAATCC AAGTCCTTGAGTCCCAACAGTCCACCTCAAA______CATACTAAAGAACAAAGGCCCCTAATCC GTTTGTC G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31829801..31830061 26863196 MeRIP-seq:(Medium) rs1425766708 Functional Loss DEL dbSNP153 32..37 33 - - - 75566 RMVar_ID_75566 Human_SNP_ID_272050829 m1A Human chr6 - 31829919 31829919 31829919 ATAGGAAAACAGCAGCAAAGTCCTTGAGTCCCAACAGTCCACCTCAAAGACAAACATACTAAAGA ATAGGAAAACAGCAGCAAAGTCCTTGAGTCCCTACAGTCCACCTCAAAGACAAACATACTAAAGA T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31829819..31829950 26863410 MeRIP-seq:(Medium) rs749927695 Functional Loss SNV dbSNP153 33..33 33 - - - 75567 RMVar_ID_75567 Human_SNP_ID_272052465 m1A Human chr6 - 31834977 31834977 31834977 GCGCAAGCCGTTGGGATCCCCTGCTCCCCCTCACTCAACAGTCGGGCCATTACAACTCTCATACT GCGCAAGCCGTTGGGATCCCCTGCTCCCCCTCGCTCAACAGTCGGGCCATTACAACTCTCATACT T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr6:31834926..31835231;chr6:31834926..31835125;chr6:31834914..31835389;chr6:31834926..31835309;chr6:31834926..31835225;chr6:31834926..31835075 26863196 MeRIP-seq:(Medium) rs1236583528 Functional Loss SNV dbSNP153 33..33 33 - - - 75568 RMVar_ID_75568 Human_SNP_ID_272052491 m1A Human chr6 + 31835024 31835024 31835024 GATCCCAACGGCTTGCGCTGCCTTTGCGCAGCAGCCGGCGGGCGGCCACGTCGCGGCCTGGCTGG GATCCCAACGGCTTGCGCTGCCTTTGCGCAGCTGCCGGCGGGCGGCCACGTCGCGGCCTGGCTGG A T SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA exon,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr6:31834926..31835078;chr6:31834926..31835088 26863196 MeRIP-seq:(Medium) rs916072413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252521,Human_RBP_ID_267302,Human_RBP_ID_661771,Human_RBP_ID_1326928,Human_RBP_ID_1395155,Human_RBP_ID_4903871,Human_RBP_ID_5122396,Human_RBP_ID_5151833,Human_RBP_ID_17663117,Human_RBP_ID_18195495,Human_RBP_ID_18425399,Human_RBP_ID_22534190,Human_RBP_ID_23214757,Human_RBP_ID_26771910 Human_Splice_Rec_754773 75569 RMVar_ID_75569 Human_SNP_ID_272052501 m1A Human chr6 - 31835050 31835050 31835050 TGCACTGGGGACCGCCCTCTCCTACCCCAGCCAGGCCGCGACGTGGCCGCCCGCCGGCTGCTGCG TGCACTGGGGACCGCCCTCTCCTACCCCAGCCGGGCCGCGACGTGGCCGCCCGCCGGCTGCTGCG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:31834948..31835094 26863410 MeRIP-seq:(Medium) rs565440664 Functional Loss SNV dbSNP153 33..33 33 - - - 75570 RMVar_ID_75570 Human_SNP_ID_272053413 m1A Human chr6 + 31837365 31837364 31837366 AGAGAAGCTTTGTATGGCTGTCATGCTTAGACAGTGATTCCTGCAACTTGACCTTCAGGCTGGGA AGAGAAGCTTTGTATGGCTGTCATGCTTAGAC__TGATTCCTGCAACTTGACCTTCAGGCTGGGA CAG C SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31837314..31837383 26863196 MeRIP-seq:(Medium) rs1374866631 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_661794,Human_RBP_ID_1671247,Human_RBP_ID_2018775,Human_RBP_ID_5152097,Human_RBP_ID_8270128,Human_RBP_ID_8642417,Human_RBP_ID_9400290,Human_RBP_ID_15788172,Human_RBP_ID_17306611,Human_RBP_ID_18863220,Human_RBP_ID_23116455,Human_RBP_ID_23214763,Human_RBP_ID_24157456,Human_RBP_ID_24512271,Human_RBP_ID_26535458,Human_RBP_ID_27754951 Human_Splice_Rec_754747,Human_Splice_Rec_754753,Human_Splice_Rec_754759,Human_Splice_Rec_754763,Human_Splice_Rec_754771,Human_Splice_Rec_754777,Human_Splice_Rec_754785,Human_Splice_Rec_754791,Human_Splice_Rec_754799,Human_Splice_Rec_754803,Human_Splice_Rec_754805 RMVar_hsa_circ_37387,RMVar_hsa_circ_55548 75571 RMVar_ID_75571 Human_SNP_ID_272053415 m1A Human chr6 + 31837365 31837365 31837365 AGAGAAGCTTTGTATGGCTGTCATGCTTAGACAGTGATTCCTGCAACTTGACCTTCAGGCTGGGA AGAGAAGCTTTGTATGGCTGTCATGCTTAGACCGTGATTCCTGCAACTTGACCTTCAGGCTGGGA A C SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31837314..31837383 26863196 MeRIP-seq:(Medium) rs145010283 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_661794,Human_RBP_ID_1671247,Human_RBP_ID_2018775,Human_RBP_ID_5152097,Human_RBP_ID_8270128,Human_RBP_ID_8642417,Human_RBP_ID_9400290,Human_RBP_ID_15788172,Human_RBP_ID_17306611,Human_RBP_ID_18863220,Human_RBP_ID_23116455,Human_RBP_ID_23214763,Human_RBP_ID_24157456,Human_RBP_ID_24512271,Human_RBP_ID_26535458,Human_RBP_ID_27754951 Human_Splice_Rec_754747,Human_Splice_Rec_754753,Human_Splice_Rec_754759,Human_Splice_Rec_754763,Human_Splice_Rec_754771,Human_Splice_Rec_754777,Human_Splice_Rec_754785,Human_Splice_Rec_754791,Human_Splice_Rec_754799,Human_Splice_Rec_754803,Human_Splice_Rec_754805 RMVar_hsa_circ_37387,RMVar_hsa_circ_55548 75572 RMVar_ID_75572 Human_SNP_ID_272059510 m1A Human chr6 + 31859439 31859439 31859439 ACAGCTCACTAGACCTGCCCAAGACAGGACCAATCAATGTCCCGGGAGGGCAGAGAGGGTGGTGG ACAGCTCACTAGACCTGCCCAAGACAGGACCAGTCAATGTCCCGGGAGGGCAGAGAGGGTGGTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:31859298..31859448 32194978 MeRIP-seq:(Medium) rs371399438 Functional Loss SNV dbSNP153 33..33 33 - - - 75573 RMVar_ID_75573 Human_SNP_ID_272059733 m1A Human chr6 - 31860160 31860160 31860160 ATTGTCCTCCGCAGCTATGATGCCTGTGATACACTAAGGCCCCGTGATGTGACCTTCGACCCTGA ATTGTCCTCCGCAGCTATGATGCCTGTGATACTCTAAGGCCCCGTGATGTGACCTTCGACCCTGA T A NEU1 Ensembl:ENSG00000204386 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31860109..31860220 26863196 MeRIP-seq:(Medium) rs1333272547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_754834 Human_miRNA_ID_218860 75574 RMVar_ID_75574 Human_SNP_ID_272064747 m1A Human chr6 - 31879959 31879959 31879959 TGCCATCTTCTCTCCCCACCACCCTTTCACACATTCCTGACCAGAGATCCCAGCCAGGCCCTGGA TGCCATCTTCTCTCCCCACCACCCTTTCACACGTTCCTGACCAGAGATCCCAGCCAGGCCCTGGA T C EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31879951..31879975 26863196 MeRIP-seq:(Medium) rs894606808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1395167,Human_RBP_ID_5122399,Human_RBP_ID_17308810,Human_RBP_ID_17419702,Human_RBP_ID_17535681,Human_RBP_ID_17663983,Human_RBP_ID_18171083,Human_RBP_ID_18195505,Human_RBP_ID_18957228,Human_RBP_ID_22424100,Human_RBP_ID_27345801,Human_RBP_ID_27526995 Human_miRNA_ID_32187,Human_miRNA_ID_554050,Human_miRNA_ID_937469 75575 RMVar_ID_75575 Human_SNP_ID_272064761 m1A Human chr6 + 31880032 31880032 31880032 AGGCATGGGCTGCGAGCAGCTGGTGGCAGAGGAGGCGGCTGAGCTGTGGCCATCCATGCTGGGGA AGGCATGGGCTGCGAGCAGCTGGTGGCAGAGGCGGCGGCTGAGCTGTGGCCATCCATGCTGGGGA A C EHMT2-AS1 Ensembl:ENSG00000237080 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31879982..31880143 26863196 MeRIP-seq:(Medium) rs188418210 Functional Loss SNV dbSNP153 33..33 33 - - - 75576 RMVar_ID_75576 Human_SNP_ID_272066047 m1A Human chr6 - 31884744 31884744 31884744 GGCCTCCTTCACGGGCAGCGCCGCCATCGCCGAAGTCCTTCTGAATGCGCGCTGTGACCTCCATG GGCCTCCTTCACGGGCAGCGCCGCCATCGCCGCAGTCCTTCTGAATGCGCGCTGTGACCTCCATG T G EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31884694..31884817 26863196 MeRIP-seq:(Medium) rs1015605210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968835,Human_RBP_ID_8900359,Human_RBP_ID_9400291,Human_RBP_ID_18195772 Human_Splice_Rec_755049,Human_Splice_Rec_755066,Human_Splice_Rec_755082,Human_Splice_Rec_755083,Human_Splice_Rec_755132,Human_Splice_Rec_755133,Human_Splice_Rec_755184,Human_Splice_Rec_755185,Human_Splice_Rec_755234,Human_Splice_Rec_755235,Human_Splice_Rec_755286,Human_Splice_Rec_755287,Human_Splice_Rec_755340,Human_Splice_Rec_755341,Human_Splice_Rec_755364,Human_Splice_Rec_755365,Human_Splice_Rec_755374 75577 RMVar_ID_75577 Human_SNP_ID_272067569 m1A Human chr6 - 31889507 31889495 31889507 GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGAAGAAGAGGAAGATGAGGAGTCAGGGAATCAGTC GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGA____________TGAGGAGTCAGGGAATCAGTC ATCTTCCTCTTCT A EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31889208..31889634 26863196 MeRIP-seq:(Medium) rs756298483 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_214859,Human_RBP_ID_792324,Human_RBP_ID_949302,Human_RBP_ID_1678489,Human_RBP_ID_3968840,Human_RBP_ID_5152102,Human_RBP_ID_7593211,Human_RBP_ID_9400299,Human_RBP_ID_17663268,Human_RBP_ID_18413845,Human_RBP_ID_18472215,Human_RBP_ID_19016718,Human_RBP_ID_23067331,Human_RBP_ID_23116426,Human_RBP_ID_23120275,Human_RBP_ID_24548380,Human_RBP_ID_25997765,Human_RBP_ID_26353163,Human_RBP_ID_27827496 Human_Splice_Rec_755108,Human_Splice_Rec_755109,Human_Splice_Rec_755160,Human_Splice_Rec_755161,Human_Splice_Rec_755212,Human_Splice_Rec_755213,Human_Splice_Rec_755264,Human_Splice_Rec_755265,Human_Splice_Rec_755316,Human_Splice_Rec_755317 75578 RMVar_ID_75578 Human_SNP_ID_272067575 m1A Human chr6 - 31889507 31889501 31889507 GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGAAGAAGAGGAAGATGAGGAGTCAGGGAATCAGTC GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGA______GGAAGATGAGGAGTCAGGGAATCAGTC CTCTTCT C EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31889208..31889634 26863196 MeRIP-seq:(Medium) rs533306500 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_214859,Human_RBP_ID_792324,Human_RBP_ID_949302,Human_RBP_ID_1678489,Human_RBP_ID_3968840,Human_RBP_ID_5152102,Human_RBP_ID_7593211,Human_RBP_ID_9400299,Human_RBP_ID_17663268,Human_RBP_ID_18413845,Human_RBP_ID_18472215,Human_RBP_ID_19016718,Human_RBP_ID_23067331,Human_RBP_ID_23116426,Human_RBP_ID_23120275,Human_RBP_ID_24548380,Human_RBP_ID_25997765,Human_RBP_ID_26353163,Human_RBP_ID_27827496 Human_Splice_Rec_755108,Human_Splice_Rec_755109,Human_Splice_Rec_755160,Human_Splice_Rec_755161,Human_Splice_Rec_755212,Human_Splice_Rec_755213,Human_Splice_Rec_755264,Human_Splice_Rec_755265,Human_Splice_Rec_755316,Human_Splice_Rec_755317 75579 RMVar_ID_75579 Human_SNP_ID_272067576 m1A Human chr6 - 31889507 31889501 31889507 GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGAAGAAGAGGAAGATGAGGAGTCAGGGAATCAGTC GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGA___AGAGGAAGATGAGGAGTCAGGGAATCAGTC CTCTTCT CTCT EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31889208..31889634 26863196 MeRIP-seq:(Medium) rs533306500 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_214859,Human_RBP_ID_792324,Human_RBP_ID_949302,Human_RBP_ID_1678489,Human_RBP_ID_3968840,Human_RBP_ID_5152102,Human_RBP_ID_7593211,Human_RBP_ID_9400299,Human_RBP_ID_17663268,Human_RBP_ID_18413845,Human_RBP_ID_18472215,Human_RBP_ID_19016718,Human_RBP_ID_23067331,Human_RBP_ID_23116426,Human_RBP_ID_23120275,Human_RBP_ID_24548380,Human_RBP_ID_25997765,Human_RBP_ID_26353163,Human_RBP_ID_27827496 Human_Splice_Rec_755108,Human_Splice_Rec_755109,Human_Splice_Rec_755160,Human_Splice_Rec_755161,Human_Splice_Rec_755212,Human_Splice_Rec_755213,Human_Splice_Rec_755264,Human_Splice_Rec_755265,Human_Splice_Rec_755316,Human_Splice_Rec_755317 75580 RMVar_ID_75580 Human_SNP_ID_272067618 m1A Human chr6 - 31889598 31889598 31889598 GGATATGTCTGTTCTGCCTCTCTCCCAGTCTGAAGTTGAAGCTCTAACTGAACAACTAAGTGAAG GGATATGTCTGTTCTGCCTCTCTCCCAGTCTGCAGTTGAAGCTCTAACTGAACAACTAAGTGAAG T G EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31889439..31889630;chr6:31889426..31889633 26863196 MeRIP-seq:(Medium) rs563393492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19130621,Human_RBP_ID_23067796,Human_RBP_ID_24548382 Human_Splice_Rec_755108,Human_Splice_Rec_755160,Human_Splice_Rec_755212,Human_Splice_Rec_755264,Human_Splice_Rec_755316 75581 RMVar_ID_75581 Human_SNP_ID_272068427 m1A Human chr6 - 31892756 31892756 31892756 TCTGTTCTGAAGGTTTCGGTGATAGGCCCCACACCATTCTCTCTCTTCTTCCAGATCTGGCCAAA TCTGTTCTGAAGGTTTCGGTGATAGGCCCCACGCCATTCTCTCTCTTCTTCCAGATCTGGCCAAA T C EHMT2 Ensembl:ENSG00000204371 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31892751..31892844 26863196 MeRIP-seq:(Medium) rs1460205031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5398067,Human_RBP_ID_22683937 Human_Splice_Rec_755105,Human_Splice_Rec_755157,Human_Splice_Rec_755209,Human_Splice_Rec_755261,Human_Splice_Rec_755313,Human_Splice_Rec_755377 RMVar_hsa_circ_237833,RMVar_hsa_circ_336873 75582 RMVar_ID_75582 Human_SNP_ID_272068465 m1A Human chr6 + 31892872 31892872 31892872 CCCAGTGAGTGGACATCATCACTCATGCGGAAATGCTGTATTTCAGGGGGCCGCTTCTCAGGGAC CCCAGTGAGTGGACATCATCACTCATGCGGAACTGCTGTATTTCAGGGGGCCGCTTCTCAGGGAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31892827..31893028 32194978 MeRIP-seq:(Medium) rs1210782083 Functional Loss SNV dbSNP153 33..33 33 - - - 75583 RMVar_ID_75583 Human_SNP_ID_272069365 m1A Human chr6 - 31896377 31896377 31896377 AGTTTGGCTATGAGGCTACTGAGTATGCCAGGAGCCCAGGGAGCTGCAGCAGCAGGGTCTGAACC AGTTTGGCTATGAGGCTACTGAGTATGCCAGGGGCCCAGGGAGCTGCAGCAGCAGGGTCTGAACC T C EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31896326..31896450 26863196 MeRIP-seq:(Medium) rs1409204754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792326,Human_RBP_ID_3969845,Human_RBP_ID_7593220,Human_RBP_ID_18472057,Human_RBP_ID_19018159 75584 RMVar_ID_75584 Human_SNP_ID_272069370 m1A Human chr6 - 31896392 31896392 31896392 CCTCCATCTGTCCAGAGTTTGGCTATGAGGCTACTGAGTATGCCAGGAGCCCAGGGAGCTGCAGC CCTCCATCTGTCCAGAGTTTGGCTATGAGGCTGCTGAGTATGCCAGGAGCCCAGGGAGCTGCAGC T C EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31896345..31896435 26863196 MeRIP-seq:(Medium) rs942314197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8642466,Human_RBP_ID_18472216 75585 RMVar_ID_75585 Human_SNP_ID_272069371 m1A Human chr6 - 31896392 31896392 31896392 CCTCCATCTGTCCAGAGTTTGGCTATGAGGCTACTGAGTATGCCAGGAGCCCAGGGAGCTGCAGC CCTCCATCTGTCCAGAGTTTGGCTATGAGGCTCCTGAGTATGCCAGGAGCCCAGGGAGCTGCAGC T G EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31896345..31896435 26863196 MeRIP-seq:(Medium) rs942314197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8642466,Human_RBP_ID_18472216 75586 RMVar_ID_75586 Human_SNP_ID_272069535 m1A Human chr6 - 31896791 31896791 31896791 TCATGGCTCTTTGGGGGACACCCCTCGTAGTGAAGAAACCCTGCCCAAGGCCACCCCCGACTCCC TCATGGCTCTTTGGGGGACACCCCTCGTAGTGGAGAAACCCTGCCCAAGGCCACCCCCGACTCCC T C EHMT2 Ensembl:ENSG00000204371 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31896677..31896845;chr6:31896651..31896827;chr6:31896711..31896838 26863196 MeRIP-seq:(Medium) rs757320153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949304,Human_RBP_ID_4882544,Human_RBP_ID_5398679,Human_RBP_ID_9400307,Human_RBP_ID_18863259,Human_RBP_ID_19018162,Human_RBP_ID_24157490,Human_RBP_ID_24387669,Human_RBP_ID_26353164,Human_RBP_ID_27827498 Human_Splice_Rec_755150,Human_Splice_Rec_755202,Human_Splice_Rec_755254,Human_Splice_Rec_755306,Human_Splice_Rec_755382 75587 RMVar_ID_75587 Human_SNP_ID_272069540 m1A Human chr6 - 31896804 31896804 31896804 CTTCCTCTACAGTTCATGGCTCTTTGGGGGACACCCCTCGTAGTGAAGAAACCCTGCCCAAGGCC CTTCCTCTACAGTTCATGGCTCTTTGGGGGACCCCCCTCGTAGTGAAGAAACCCTGCCCAAGGCC T G EHMT2 Ensembl:ENSG00000204371 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31896502..31897008 26863196 MeRIP-seq:(Medium) rs754827811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949304,Human_RBP_ID_1046951,Human_RBP_ID_1326944,Human_RBP_ID_4903874,Human_RBP_ID_5398679,Human_RBP_ID_7593223,Human_RBP_ID_9400307,Human_RBP_ID_19018162,Human_RBP_ID_24157490,Human_RBP_ID_24387669,Human_RBP_ID_26353164,Human_RBP_ID_27827498 Human_Splice_Rec_755150,Human_Splice_Rec_755202,Human_Splice_Rec_755254,Human_Splice_Rec_755306,Human_Splice_Rec_755382 75588 RMVar_ID_75588 Human_SNP_ID_272069798 m1A Human chr6 - 31897295 31897295 31897295 TTGGTGCCCGGGGTCCCCGCGGCCTGGGGGACAAAGGGGGAGCGGCGCGTGCAGCCGGGAGGAGG TTGGTGCCCGGGGTCCCCGCGGCCTGGGGGACGAAGGGGGAGCGGCGCGTGCAGCCGGGAGGAGG T C EHMT2 Ensembl:ENSG00000204371 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31897291..31897658 26863196 MeRIP-seq:(Medium) rs1297035136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947508,Human_RBP_ID_3821150,Human_RBP_ID_5400495,Human_RBP_ID_8215176,Human_RBP_ID_9437400,Human_RBP_ID_18957232,Human_RBP_ID_19128976,Human_RBP_ID_21990743,Human_RBP_ID_26792964 75589 RMVar_ID_75589 Human_SNP_ID_272069815 m1A Human chr6 - 31897370 31897370 31897370 CCGGGGCCCCAGGAGCACGCGTGAGGGGCACGAGGGGCCGTCCACCGGGCTGGGGGGCAGCGGGT CCGGGGCCCCAGGAGCACGCGTGAGGGGCACGGGGGGCCGTCCACCGGGCTGGGGGGCAGCGGGT T C EHMT2 Ensembl:ENSG00000204371 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31897367..31897700 26863196 MeRIP-seq:(Medium) rs1199829204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9437401,Human_RBP_ID_19130626,Human_RBP_ID_21990744,Human_RBP_ID_26792595 75590 RMVar_ID_75590 Human_SNP_ID_272070331 m1A Human chr6 + 31899319 31899319 31899319 ATTGTACCCCCACTTCCCAATATCTACCCAGGATGCGCACCCCACGTTCTCTTACCTGGCGTCTT ATTGTACCCCCACTTCCCAATATCTACCCAGGGTGCGCACCCCACGTTCTCTTACCTGGCGTCTT A G C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31899270..31899475 26863196 MeRIP-seq:(Medium) rs1213271619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18957234 75591 RMVar_ID_75591 Human_SNP_ID_272070404 m1A Human chr6 + 31899627 31899625 31899627 AGGAATAAAACATTTTTGTCTTCCCTCATTCTATAGGACCCTTTTCCCTCCCTCCACATATACAT AGGAATAAAACATTTTTGTCTTCCCTCATTC__TAGGACCCTTTTCCCTCCCTCCACATATACAT CTA C C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31899577..31899766 26863196 MeRIP-seq:(Medium) rs1157452503 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3003426,Human_RBP_ID_3806493 75592 RMVar_ID_75592 Human_SNP_ID_272070458 m1A Human chr6 + 31899881 31899881 31899881 CCAATTCTCCTGGGCCAAAGAGCCCTTTTTCCACGCAGCCCAGGGGCCCCAGCCTCCTGGCCTCC CCAATTCTCCTGGGCCAAAGAGCCCTTTTTCCCCGCAGCCCAGGGGCCCCAGCCTCCTGGCCTCC A C C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31899831..31899991 26863196 MeRIP-seq:(Medium) rs1413153976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821587,Human_RBP_ID_5134116,Human_RBP_ID_17091710 75593 RMVar_ID_75593 Human_SNP_ID_272070621 m1A Human chr6 - 31900447 31900447 31900447 AGGGCCTGCTGTTGATTCCCGGAGGCCGGGCCAGCGTGGGGGCCACCTCGGGCCTGGTGGAAGCA AGGGCCTGCTGTTGATTCCCGGAGGCCGGGCCTGCGTGGGGGCCACCTCGGGCCTGGTGGAAGCA T A ZBTB12 Ensembl:ENSG00000204366 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31900405..31900487 26863196 MeRIP-seq:(Medium) rs1371384570 Functional Loss SNV dbSNP153 33..33 33 - - - 75594 RMVar_ID_75594 Human_SNP_ID_272071108 m1A Human chr6 + 31901901 31901901 31901901 CCTTATTTTCCCCACCCCCCCCCGGGGCCGGCAGCGACCCCCACACACGGGCAGGGCCTGGGCAG CCTTATTTTCCCCACCCCCCCCCGGGGCCGGCGGCGACCCCCACACACGGGCAGGGCCTGGGCAG A G C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31901810..31902027 26863196 MeRIP-seq:(Medium) rs1388524283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252357,Human_RBP_ID_24436693,Human_RBP_ID_26792969 75595 RMVar_ID_75595 Human_SNP_ID_272071109 m1A Human chr6 + 31901901 31901901 31901901 CCTTATTTTCCCCACCCCCCCCCGGGGCCGGCAGCGACCCCCACACACGGGCAGGGCCTGGGCAG CCTTATTTTCCCCACCCCCCCCCGGGGCCGGCTGCGACCCCCACACACGGGCAGGGCCTGGGCAG A T C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31901810..31902027 26863196 MeRIP-seq:(Medium) rs1388524283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252357,Human_RBP_ID_24436693,Human_RBP_ID_26792969 75596 RMVar_ID_75596 Human_SNP_ID_272071125 m1A Human chr6 + 31901958 31901932 31901959 CTGGGCAGCGCGCAGGCGCGGGGATGCACGGGACGCGCGCGCGCGCGGGGCCGGCTCCGCGTGGG CTGGGCA___________________________GCGCGCGCGCGCGGGGCCGGCTCCGCGTGGG AGCGCGCAGGCGCGGGGATGCACGGGAC A C2 Ensembl:ENSG00000166278 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31901925..31902177 26863196 MeRIP-seq:(Medium) rs1316632027 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_8215181 75597 RMVar_ID_75597 Human_SNP_ID_272083233 m1A Human chr6 - 31952327 31952327 31952327 GGACCCAGATTGTCTACAGTGATGACGTCTACAAGGAAAACCTTGTGGATGGCTTCTAGGGAACA GGACCCAGATTGTCTACAGTGATGACGTCTACCAGGAAAACCTTGTGGATGGCTTCTAGGGAACA T G NELFE Ensembl:ENSG00000204356 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:31952276..31952375;chr6:31952276..31953775 32194978 MeRIP-seq:(Medium) rs781245821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661872,Human_RBP_ID_1671286,Human_RBP_ID_2018828,Human_RBP_ID_3806508,Human_RBP_ID_8642503,Human_RBP_ID_9193584,Human_RBP_ID_18863284 Human_Splice_Rec_755952,Human_Splice_Rec_755968,Human_Splice_Rec_755984,Human_Splice_Rec_756002,Human_Splice_Rec_756022,Human_Splice_Rec_756042 75598 RMVar_ID_75598 Human_SNP_ID_272083849 m1A Human chr6 - 31954657 31954652 31954658 AGCGGGATCGAGACCGGGATCGAGACAGAGACAGAGAGCGGGACAGGGATCGGGATCGGGATCGA AGCGGGATCGAGACCGGGATCGAGACAGAGA______GCGGGACAGGGATCGGGATCGGGATCGA CTCTCTG C NELFE Ensembl:ENSG00000204356 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31954606..31954804 26863196 MeRIP-seq:(Medium) rs759478514 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_4882678,Human_RBP_ID_9193585,Human_RBP_ID_19016734,Human_RBP_ID_22462636,Human_RBP_ID_23067800,Human_RBP_ID_26353711 75599 RMVar_ID_75599 Human_SNP_ID_272083861 m1A Human chr6 - 31954697 31954673 31954697 CGCAGCCATGAGAGGAACCGGGACAGAGACCGAGATCGGGAGCGGGATCGAGACCGGGATCGAGA CGCAGCCATGAGAGGAACCGGGACAGAGACCG________________________GGATCGAGA CCGGTCTCGATCCCGCTCCCGATCT C NELFE Ensembl:ENSG00000204356 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31954543..31954826 26863196 MeRIP-seq:(Medium) rs758227767 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_661889,Human_RBP_ID_4882680,Human_RBP_ID_9309674,Human_RBP_ID_9400315,Human_RBP_ID_19016734,Human_RBP_ID_26353711,Human_RBP_ID_27828441 75600 RMVar_ID_75600 Human_SNP_ID_272083879 m1A Human chr6 + 31954694 31954694 31954694 CTGTCTCGATCCCGGTCTCGATCCCGCTCCCGATCTCGGTCTCTGTCCCGGTTCCTCTCATGGCT CTGTCTCGATCCCGGTCTCGATCCCGCTCCCGCTCTCGGTCTCTGTCCCGGTTCCTCTCATGGCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31954643..31954790 26863196 MeRIP-seq:(Medium) rs867135503 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 75601 RMVar_ID_75601 Human_SNP_ID_272083929 m1A Human chr6 + 31954801 31954801 31954801 GGCACCACTGCGTTCTTCATAGCCCCAGTCAAAGCTTCGAGGGGGACCATCACCAGCCCCTGGGC GGCACCACTGCGTTCTTCATAGCCCCAGTCAAGGCTTCGAGGGGGACCATCACCAGCCCCTGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31954751..31954927 32194978 MeRIP-seq:(Medium) rs1249879821 Functional Loss SNV dbSNP153 33..33 33 - - - 75602 RMVar_ID_75602 Human_SNP_ID_272084913 m1A Human chr6 - 31958456 31958456 31958456 GAGAAAGATGTCTTGGGCCCTGCCCCTGAACTAGGAGCCACCATGTTGGTGATACCCCCCGGACT GAGAAAGATGTCTTGGGCCCTGCCCCTGAACTCGGAGCCACCATGTTGGTGATACCCCCCGGACT T G NELFE Ensembl:ENSG00000204356 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31958436..31958575 26863196 MeRIP-seq:(Medium) rs1398902752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948626,Human_RBP_ID_4905433,Human_RBP_ID_5327114,Human_RBP_ID_9336075,Human_RBP_ID_27096389 Human_Splice_Rec_755935,Human_Splice_Rec_755955,Human_Splice_Rec_755969,Human_Splice_Rec_755987,Human_Splice_Rec_756005,Human_Splice_Rec_756025,Human_Splice_Rec_756045,Human_Splice_Rec_756061,Human_Splice_Rec_756073,Human_Splice_Rec_756099,Human_Splice_Rec_756111,Human_Splice_Rec_756119,Human_Splice_Rec_756127 75603 RMVar_ID_75603 Human_SNP_ID_272085065 m1A Human chr6 - 31958924 31958924 31958924 CCGCTATCAGCGGCCAGCGCGGGCGCGGCCGGAGACCGTGGGGCCCCCGGTTGCCGCCCCCTCGG CCGCTATCAGCGGCCAGCGCGGGCGCGGCCGGGGACCGTGGGGCCCCCGGTTGCCGCCCCCTCGG T C NELFE Ensembl:ENSG00000204356 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31958855..31958975 26863196 MeRIP-seq:(Medium) rs886061299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252514,Human_RBP_ID_4882699,Human_RBP_ID_18425402 Human_Splice_Rec_755933,Human_Splice_Rec_755953,Human_Splice_Rec_755985,Human_Splice_Rec_756023,Human_Splice_Rec_756043,Human_Splice_Rec_756085,Human_Splice_Rec_756109,Human_Splice_Rec_756117 Clinvar_Rec_346 75604 RMVar_ID_75604 Human_SNP_ID_272085267 m1A Human chr6 + 31959395 31959394 31959395 GGGAGCTGCTGAACTTGCCTGGAGCTCCAGAGAGTAGCGTGAGTGACTTTTGACCCTAACCTTTG GGGAGCTGCTGAACTTGCCTGGAGCTCCAGAG_GTAGCGTGAGTGACTTTTGACCCTAACCTTTG GA G SKIV2L Ensembl:ENSG00000204351 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31959276..31959425 26863196 MeRIP-seq:(Medium) rs1562650465 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8642515 Human_Splice_Rec_756130,Human_Splice_Rec_756131,Human_Splice_Rec_756144,Human_Splice_Rec_756145,Human_Splice_Rec_756188,Human_Splice_Rec_756189,Human_Splice_Rec_756208,Human_Splice_Rec_756209,Human_Splice_Rec_756254,Human_Splice_Rec_756255,Human_Splice_Rec_756308,Human_Splice_Rec_756310,Human_Splice_Rec_756311 75605 RMVar_ID_75605 Human_SNP_ID_272085476 m1A Human chr6 + 31960274 31960274 31960274 CCCTGGTCTCTTTTGGCTGTCCTGGGAGCCCCAGTCCCATCCGACCTACAGGCCCAAAGACACCC CCCTGGTCTCTTTTGGCTGTCCTGGGAGCCCCGGTCCCATCCGACCTACAGGCCCAAAGACACCC A G SKIV2L Ensembl:ENSG00000204351 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31960203..31960276 26863196 MeRIP-seq:(Medium) rs1418291658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947510,Human_RBP_ID_3968848,Human_RBP_ID_9400320,Human_RBP_ID_19016745,Human_RBP_ID_22461948,Human_RBP_ID_23067801,Human_RBP_ID_26353166,Human_RBP_ID_27827503 Human_Splice_Rec_756134,Human_Splice_Rec_756135,Human_Splice_Rec_756148,Human_Splice_Rec_756149,Human_Splice_Rec_756192,Human_Splice_Rec_756193,Human_Splice_Rec_756258,Human_Splice_Rec_756259 75606 RMVar_ID_75606 Human_SNP_ID_272087527 m1A Human chr6 + 31967098 31967098 31967098 GACTGGCCAACTGGTCGACCTGCCTGAATATTACAGCTGGGGGGAGGAACTGACAGAGACCCAGC GACTGGCCAACTGGTCGACCTGCCTGAATATTGCAGCTGGGGGGAGGAACTGACAGAGACCCAGC A G SKIV2L Ensembl:ENSG00000204351 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31967048..31967167 26863196 MeRIP-seq:(Medium) rs141771835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_314037,Human_RBP_ID_790714,Human_RBP_ID_4882743,Human_RBP_ID_8270131,Human_RBP_ID_23067803 Human_Splice_Rec_756174,Human_Splice_Rec_756175,Human_Splice_Rec_756236,Human_Splice_Rec_756237,Human_Splice_Rec_756290,Human_Splice_Rec_756291,Human_Splice_Rec_756324,Human_Splice_Rec_756325,Human_Splice_Rec_756331,Human_Splice_Rec_756337 RMVar_hsa_circ_237835,RMVar_hsa_circ_86664 75607 RMVar_ID_75607 Human_SNP_ID_272088765 m1A Human chr6 + 31970727 31970725 31970727 TTGGGGGTCTGTGCAGTCTACCTCCCCTGAGAAGAGCAGAGGGTGGCTTCCCAGGCGGCTGCGTA TTGGGGGTCTGTGCAGTCTACCTCCCCTGAG__GAGCAGAGGGTGGCTTCCCAGGCGGCTGCGTA GAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31970677..31970762 26863196 MeRIP-seq:(Medium) rs764580568 Functional Loss DEL dbSNP153 32..33 33 - - - 75608 RMVar_ID_75608 Human_SNP_ID_272089101 m1A Human chr6 + 31971493 31971493 31971493 GGGCTATAGTAGCGCAGGGCTCGGGCATCTCCATGGTACTGGCGTTGAGCATCCAGGGAGAAGCA GGGCTATAGTAGCGCAGGGCTCGGGCATCTCCCTGGTACTGGCGTTGAGCATCCAGGGAGAAGCA A C STK19 Ensembl:ENSG00000204344 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31971445..31971650 26863196 MeRIP-seq:(Medium) rs772615090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791754,Human_RBP_ID_8215966 75609 RMVar_ID_75609 Human_SNP_ID_272089102 m1A Human chr6 + 31971493 31971493 31971493 GGGCTATAGTAGCGCAGGGCTCGGGCATCTCCATGGTACTGGCGTTGAGCATCCAGGGAGAAGCA GGGCTATAGTAGCGCAGGGCTCGGGCATCTCCGTGGTACTGGCGTTGAGCATCCAGGGAGAAGCA A G STK19 Ensembl:ENSG00000204344 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31971445..31971650 26863196 MeRIP-seq:(Medium) rs772615090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791754,Human_RBP_ID_8215966 75610 RMVar_ID_75610 Human_SNP_ID_272089483 m1A Human chr6 - 31972449 31972449 31972449 CAGGCCCTCGCTTCCGCCGCCTCTTAACTCCAAAGGTCTCCGGGATCAGGTGATGCCTCTTCCAG CAGGCCCTCGCTTCCGCCGCCTCTTAACTCCATAGGTCTCCGGGATCAGGTGATGCCTCTTCCAG T A RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31972398..31972680 26863196 MeRIP-seq:(Medium) rs766530771 Functional Loss SNV dbSNP153 33..33 33 - - - 75611 RMVar_ID_75611 Human_SNP_ID_272089484 m1A Human chr6 - 31972449 31972449 31972449 CAGGCCCTCGCTTCCGCCGCCTCTTAACTCCAAAGGTCTCCGGGATCAGGTGATGCCTCTTCCAG CAGGCCCTCGCTTCCGCCGCCTCTTAACTCCAGAGGTCTCCGGGATCAGGTGATGCCTCTTCCAG T C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31972398..31972680 26863196 MeRIP-seq:(Medium) rs766530771 Functional Loss SNV dbSNP153 33..33 33 - - - 75612 RMVar_ID_75612 Human_SNP_ID_272089702 m1A Human chr6 + 31973033 31973032 31973034 ACAGCGCTGGGAGTGCAGTCAGACGTCAGATCATGACAGGCCTTGTACATCAGTGTTGTTTCCAT ACAGCGCTGGGAGTGCAGTCAGACGTCAGATC__GACAGGCCTTGTACATCAGTGTTGTTTCCAT CAT C STK19 Ensembl:ENSG00000204344 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31973027..31973299 26863196 MeRIP-seq:(Medium) rs1404307918 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15788980 75613 RMVar_ID_75613 Human_SNP_ID_272113810 m1A Human chr6 - 32096207 32096207 32096207 CGAGGATGGCGTGTGCGTGTGTGACGCAGGCTACTCAGGGGAAGACTGCAGCACGCGCAGCTGCC CGAGGATGGCGTGTGCGTGTGTGACGCAGGCTCCTCAGGGGAAGACTGCAGCACGCGCAGCTGCC T G TNXB Ensembl:ENSG00000168477 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32096158..32096324 32194978 MeRIP-seq:(Medium) rs1429534356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24157578 RMVar_hsa_circ_265629 75614 RMVar_ID_75614 Human_SNP_ID_272117164 m1A Human chr6 - 32108809 32108809 32108809 TGGGCCCTGGAGGTGCTGGGGCTAGCGGGAAGATAGGACTAGGCTGAACTGGTGGCCAGCTGAAC TGGGCCCTGGAGGTGCTGGGGCTAGCGGGAAGGTAGGACTAGGCTGAACTGGTGGCCAGCTGAAC T C TNXB,AL662884.2 Ensembl:ENSG00000168477,Ensembl:ENSG00000284829 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32108805..32108993 26863196 MeRIP-seq:(Medium) rs1269333637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3823318,Human_RBP_ID_5620815,Human_RBP_ID_8216932,Human_RBP_ID_8642549,Human_RBP_ID_26792986 75615 RMVar_ID_75615 Human_SNP_ID_272118677 m1A Human chr6 + 32115840 32115840 32115840 GGGGCCACCTGTGGCATTGCCTGGGGTTGGGGATGGCTGTTTTCGGAGCGAGGGGGGCACTGTGG GGGGCCACCTGTGGCATTGCCTGGGGTTGGGGGTGGCTGTTTTCGGAGCGAGGGGGGCACTGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32115791..32115956 26863196 MeRIP-seq:(Medium) rs1397269164 Functional Loss SNV dbSNP153 33..33 33 - - - 75616 RMVar_ID_75616 Human_SNP_ID_272118705 m1A Human chr6 + 32115910 32115910 32115910 TTGATGTGAATCACCCTGGTGTCCATGACCTCACACTCGATCTGCATCATCTCCTCATAGTCCCC TTGATGTGAATCACCCTGGTGTCCATGACCTCGCACTCGATCTGCATCATCTCCTCATAGTCCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32115677..32116486 32194978 MeRIP-seq:(Medium) rs377004959 Functional Loss SNV dbSNP153 33..33 33 - - - 75617 RMVar_ID_75617 Human_SNP_ID_272118738 m1A Human chr6 + 32115984 32115984 32115984 ACGGCCTGACAGGGTCTCTGTGAGAAGGGGAGAGTTAAGGAAGAGGAGATGGGGAGGCAAACAGG ACGGCCTGACAGGGTCTCTGTGAGAAGGGGAGGGTTAAGGAAGAGGAGATGGGGAGGCAAACAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:32115976..32116000 26863196 MeRIP-seq:(Medium) rs745984667 Functional Loss SNV dbSNP153 33..33 33 - - - 75618 RMVar_ID_75618 Human_SNP_ID_272118799 m1A Human chr6 - 32116304 32116304 32116304 GAGCACCATGCAGGAGACTTGGGAGGGAGACAAGGGTGAGGGTCCTTCCCTGGTGAAGGTGCTTG GAGCACCATGCAGGAGACTTGGGAGGGAGACAGGGGTGAGGGTCCTTCCCTGGTGAAGGTGCTTG T C AL662884.2,ATF6B Ensembl:ENSG00000284829,Ensembl:ENSG00000213676 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:32116257..32116441 26863196 MeRIP-seq:(Medium) rs375324796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13402,Human_RBP_ID_1678752,Human_RBP_ID_3823305,Human_RBP_ID_5242678,Human_RBP_ID_5398694,Human_RBP_ID_5619415,Human_RBP_ID_8217109,Human_RBP_ID_18171432,Human_RBP_ID_18957242,Human_RBP_ID_22618194 75619 RMVar_ID_75619 Human_SNP_ID_272118847 m1A Human chr6 - 32116530 32116530 32116530 CCACCTGCTGCTCCCAGCCATCAGCCACAACAAGACCTCCCGGCCCAAGATGTCCCTGGTGATGC CCACCTGCTGCTCCCAGCCATCAGCCACAACACGACCTCCCGGCCCAAGATGTCCCTGGTGATGC T G AL662884.2,ATF6B Ensembl:ENSG00000284829,Ensembl:ENSG00000213676 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32116330..32116582 26863196 MeRIP-seq:(Medium) rs1485436101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5122189,Human_RBP_ID_9401911,Human_RBP_ID_19129025,Human_RBP_ID_26829454 Human_Splice_Rec_757936,Human_Splice_Rec_757937,Human_Splice_Rec_757970,Human_Splice_Rec_757971,Human_Splice_Rec_758004,Human_Splice_Rec_758005 75620 RMVar_ID_75620 Human_SNP_ID_272120039 m1A Human chr6 - 32120849 32120849 32120849 AGCCGCCACTGCAGCCCAAACCTGTAGTGCTAACCACTGTCCCAATGCCATCCAGAGCTGTGCCT AGCCGCCACTGCAGCCCAAACCTGTAGTGCTAGCCACTGTCCCAATGCCATCCAGAGCTGTGCCT T C ATF6B Ensembl:ENSG00000213676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32120758..32121057 26863196 MeRIP-seq:(Medium) rs1159235686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15789316,Human_RBP_ID_17091179,Human_RBP_ID_17308816 Human_Splice_Rec_757918,Human_Splice_Rec_757919,Human_Splice_Rec_757952,Human_Splice_Rec_757953,Human_Splice_Rec_757986,Human_Splice_Rec_757987,Human_Splice_Rec_758026,Human_Splice_Rec_758038 Human_miRNA_ID_2057505,Human_miRNA_ID_2057506 RMVar_hsa_circ_79361,RMVar_hsa_circ_237837,RMVar_hsa_circ_320396,RMVar_hsa_circ_49046,RMVar_hsa_circ_336883,RMVar_hsa_circ_237838 75621 RMVar_ID_75621 Human_SNP_ID_272121346 m1A Human chr6 - 32126179 32126179 32126179 CTTGGCACCCCCACTGTGTCTCCTGGGAGATGACCCAACATCCTCATTTGAAACCGTCCAGATCA CTTGGCACCCCCACTGTGTCTCCTGGGAGATGGCCCAACATCCTCATTTGAAACCGTCCAGATCA T C ATF6B Ensembl:ENSG00000213676 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32126083..32126275 26863196 MeRIP-seq:(Medium) rs1404631740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661937,Human_RBP_ID_1046980,Human_RBP_ID_9193591,Human_RBP_ID_18413847,Human_RBP_ID_18539076 Human_Splice_Rec_757912,Human_Splice_Rec_757913,Human_Splice_Rec_757946,Human_Splice_Rec_757947,Human_Splice_Rec_757980,Human_Splice_Rec_757981,Human_Splice_Rec_758020,Human_Splice_Rec_758021,Human_Splice_Rec_758032,Human_Splice_Rec_758033,Human_Splice_Rec_758046 RMVar_hsa_circ_336883,RMVar_hsa_circ_42177 75622 RMVar_ID_75622 Human_SNP_ID_272121669 m1A Human chr6 + 32127428 32127427 32127429 GATGAGGGTTTCTGGAAATCTGAGGGAACGACAAAGACTACCTTACCTGGGAAGATCGGCAGGAG GATGAGGGTTTCTGGAAATCTGAGGGAACGAC__AGACTACCTTACCTGGGAAGATCGGCAGGAG CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32127426..32127525 26863196 MeRIP-seq:(Medium) rs1462422744 Functional Loss DEL dbSNP153 33..34 33 - - - 75623 RMVar_ID_75623 Human_SNP_ID_272121679 m1A Human chr6 - 32127461 32127461 32127461 ATGGATGTCAGCCCCTCTGAGCCCCCATGGGAACTCCTGCCGATCTTCCCAGGTAAGGTAGTCTT ATGGATGTCAGCCCCTCTGAGCCCCCATGGGAGCTCCTGCCGATCTTCCCAGGTAAGGTAGTCTT T C ATF6B Ensembl:ENSG00000213676 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32127456..32127706 32194978 MeRIP-seq:(Medium) rs770891500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661939,Human_RBP_ID_18863367,Human_RBP_ID_19018251 Human_Splice_Rec_757908,Human_Splice_Rec_757909,Human_Splice_Rec_757942,Human_Splice_Rec_757943,Human_Splice_Rec_757976,Human_Splice_Rec_757977,Human_Splice_Rec_758016,Human_Splice_Rec_758017,Human_Splice_Rec_758028,Human_Splice_Rec_758029,Human_Splice_Rec_758042,Human_Splice_Rec_758043 75624 RMVar_ID_75624 Human_SNP_ID_272121938 m1A Human chr6 - 32128200 32128200 32128200 CCTGGTTGGGGGGTGGGGGGGAAAGATGGCGGAGCTGATGCTGCTCAGCGAGATTGCTGACCCGA CCTGGTTGGGGGGTGGGGGGGAAAGATGGCGGCGCTGATGCTGCTCAGCGAGATTGCTGACCCGA T G ATF6B Ensembl:ENSG00000213676 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:32128018..32128225 26863196 MeRIP-seq:(Medium) rs755108438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252711,Human_RBP_ID_791461,Human_RBP_ID_4903886,Human_RBP_ID_8905772,Human_RBP_ID_9336078,Human_RBP_ID_9438394,Human_RBP_ID_18425405,Human_RBP_ID_25998087 Human_Splice_Rec_757905,Human_Splice_Rec_757939,Human_Splice_Rec_757973,Human_Splice_Rec_758013,Human_Splice_Rec_758039 75625 RMVar_ID_75625 Human_SNP_ID_272122532 m1A Human chr6 + 32130276 32130276 32130276 CGGGGGTAGGGGGCGGAACAACTGGGAAAGATACTGACAACTAACCCTGGAGCCCGCGAGACTCC CGGGGGTAGGGGGCGGAACAACTGGGAAAGATGCTGACAACTAACCCTGGAGCCCGCGAGACTCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:32130255..32130343 26863410 MeRIP-seq:(Medium) rs1425930018 Functional Loss SNV dbSNP153 33..33 33 - - - 75626 RMVar_ID_75626 Human_SNP_ID_272127379 m1A Human chr6 + 32151980 32151976 32151980 CGGCGGGGGGGGGGGGCGGGGGGGGCGGGCGGAGGGAGAGCGGGGAGGGGGGGAGCTTAAAGGGA CGGCGGGGGGGGGGGGCGGGGGGGGCGGG____GGGAGAGCGGGGAGGGGGGGAGCTTAAAGGGA GCGGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:32151763..32151989;chr6:32151863..32152000 26863196 MeRIP-seq:(Medium) rs1561803913 Functional Loss DEL dbSNP153 30..33 33 - - - 75627 RMVar_ID_75627 Human_SNP_ID_272127382 m1A Human chr6 + 32151980 32151980 32151980 CGGCGGGGGGGGGGGGCGGGGGGGGCGGGCGGAGGGAGAGCGGGGAGGGGGGGAGCTTAAAGGGA CGGCGGGGGGGGGGGGCGGGGGGGGCGGGCGGGGGGAGAGCGGGGAGGGGGGGAGCTTAAAGGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:32151763..32151989;chr6:32151863..32152000 26863196 MeRIP-seq:(Medium) rs1008484977 Functional Loss SNV dbSNP153 33..33 33 - - - 75628 RMVar_ID_75628 Human_SNP_ID_272127386 m1A Human chr6 + 32151984 32151984 32151984 GGGGGGGGGGGGCGGGGGGGGCGGGCGGAGGGAGAGCGGGGAGGGGGGGAGCTTAAAGGGACCGA GGGGGGGGGGGGCGGGGGGGGCGGGCGGAGGGGGAGCGGGGAGGGGGGGAGCTTAAAGGGACCGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:32151860..32152000 26863196 MeRIP-seq:(Medium) rs1201318789 Functional Loss SNV dbSNP153 33..33 33 - - - 75629 RMVar_ID_75629 Human_SNP_ID_272127786 m1A Human chr6 - 32153773 32153773 32153773 GCATTCCCCAAGGGGCGGCCAGGGGGCGGACCAGGGAAAGGTAGTCCTCTGCATTTTGCCGTGTG GCATTCCCCAAGGGGCGGCCAGGGGGCGGACCGGGGAAAGGTAGTCCTCTGCATTTTGCCGTGTG T C AL662884.4,AL662884.3 Ensembl:ENSG00000285085,Ensembl:ENSG00000284954 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32153768..32153867 26863196 MeRIP-seq:(Medium) rs1484918451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5621896 Human_Splice_Rec_758076,Human_Splice_Rec_758077,Human_Splice_Rec_758083,Human_Splice_Rec_758087,Human_Splice_Rec_758090,Human_Splice_Rec_758091,Human_Splice_Rec_758094,Human_Splice_Rec_758095,Human_Splice_Rec_758098,Human_Splice_Rec_758099,Human_Splice_Rec_758102,Human_Splice_Rec_758103 75630 RMVar_ID_75630 Human_SNP_ID_272129975 m1A Human chr6 - 32162844 32162844 32162844 CCATTGGACACCTCACTATGGCCCCCCGGGCCAATAGAGTCTTCAACCCAAAAGAATCCCGCAGA CCATTGGACACCTCACTATGGCCCCCCGGGCCCATAGAGTCTTCAACCCAAAAGAATCCCGCAGA T G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32162801..32162975 32194978 MeRIP-seq:(Medium) rs765235405 Functional Loss SNV dbSNP153 33..33 33 - - - 75631 RMVar_ID_75631 Human_SNP_ID_272130062 m1A Human chr6 - 32163179 32163179 32163179 TGAGAGAAAGGGACAGCACGGAGCAATCCCCCAAATGAGAGGACATGAGGTAGGGGAGGCCTGGA TGAGAGAAAGGGACAGCACGGAGCAATCCCCCGAATGAGAGGACATGAGGTAGGGGAGGCCTGGA T C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:32163176..32163200 26863196 MeRIP-seq:(Medium) rs1389828571 Functional Loss SNV dbSNP153 33..33 33 - - - 75632 RMVar_ID_75632 Human_SNP_ID_272131248 m1A Human chr6 + 32167425 32167425 32167425 TCACGAGCTGCGAGGGCGCCTGGAGCGGCTGGAGCAGGTGAGCCAAGCCTGCTGGGTGGGGCGAG TCACGAGCTGCGAGGGCGCCTGGAGCGGCTGGGGCAGGTGAGCCAAGCCTGCTGGGTGGGGCGAG A G EGFL8,PPT2-EGFL8 Ensembl:ENSG00000241404,Ensembl:ENSG00000258388 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32167376..32167603 26863196 MeRIP-seq:(Medium) rs199614917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949354,Human_RBP_ID_3968893,Human_RBP_ID_9401924,Human_RBP_ID_19018266,Human_RBP_ID_19130687,Human_RBP_ID_22618203,Human_RBP_ID_26792991 Human_Splice_Rec_758266,Human_Splice_Rec_758267,Human_Splice_Rec_758310,Human_Splice_Rec_758311,Human_Splice_Rec_758388,Human_Splice_Rec_758389,Human_Splice_Rec_758402,Human_Splice_Rec_758403,Human_Splice_Rec_758416,Human_Splice_Rec_758417,Human_Splice_Rec_758426 75633 RMVar_ID_75633 Human_SNP_ID_272131699 m1A Human chr6 + 32169234 32169230 32169234 CTTCAGGGCCCACTGGGTGGGTAGGTGTGGGGAGGAAGATGGGGACAGATGGGAGGAGAGCTCAG CTTCAGGGCCCACTGGGTGGGTAGGTGTG____GGAAGATGGGGACAGATGGGAGGAGAGCTCAG GGGGA G PPT2-EGFL8 Ensembl:ENSG00000258388 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:32169007..32169275;chr6:32168056..32171375 32194978 MeRIP-seq:(Medium) rs775831642 Functional Loss DEL dbSNP153 30..33 33 - - - 75634 RMVar_ID_75634 Human_SNP_ID_272131936 m1A Human chr6 + 32170219 32170219 32170219 AAGGCGCCACGTTTGAAGGGCAGCATGGAGCCATTGTGGTTTCTCGTTCCCTCAGGAAACACCCA AAGGCGCCACGTTTGAAGGGCAGCATGGAGCCTTTGTGGTTTCTCGTTCCCTCAGGAAACACCCA A T PPT2-EGFL8 Ensembl:ENSG00000258388 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32170168..32170274 26863196 MeRIP-seq:(Medium) rs765822175 Functional Loss SNV dbSNP153 33..33 33 - - - 75635 RMVar_ID_75635 Human_SNP_ID_272132246 m1A Human chr6 + 32171456 32171456 32171456 GGGTGGGCAGCAGGAAGAGCAGCAGCAGGAAGAGCAGCAGCAGCAGCATCCATGCCCCTGGCCAC GGGTGGGCAGCAGGAAGAGCAGCAGCAGGAAGGGCAGCAGCAGCAGCATCCATGCCCCTGGCCAC A G PPT2-EGFL8 Ensembl:ENSG00000258388 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32171342..32171528 26863196 MeRIP-seq:(Medium) rs977923338 Functional Loss SNV dbSNP153 33..33 33 - - - 75636 RMVar_ID_75636 Human_SNP_ID_272133057 m1A Human chr6 - 32176036 32176036 32176036 CCAGCCCTCAGAGAGACAGCAGAAAGGGAGGGAGGGAGGGTGCTGGGGGGACAGCCCCCCACCAT CCAGCCCTCAGAGAGACAGCAGAAAGGGAGGGGGGGAGGGTGCTGGGGGGACAGCCCCCCACCAT T C AGPAT1 Ensembl:ENSG00000204310 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:32175826..32176050 26863196 MeRIP-seq:(Medium) rs1392711921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903241 Human_miRNA_ID_545573,Human_miRNA_ID_580810 75637 RMVar_ID_75637 Human_SNP_ID_272133061 m1A Human chr6 - 32176044 32176044 32176044 CAGCAGCCCCAGCCCTCAGAGAGACAGCAGAAAGGGAGGGAGGGAGGGTGCTGGGGGGACAGCCC CAGCAGCCCCAGCCCTCAGAGAGACAGCAGAAGGGGAGGGAGGGAGGGTGCTGGGGGGACAGCCC T C AGPAT1 Ensembl:ENSG00000204310 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:32175944..32176091 26863410 MeRIP-seq:(Medium) rs1443216887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4912249 Human_miRNA_ID_545573,Human_miRNA_ID_580810 75638 RMVar_ID_75638 Human_SNP_ID_272133180 m1A Human chr6 - 32176611 32176611 32176611 GGGAGCTGGACTGCTGGGAGATAGTGAGGGACAAAGGGCAAAGGAAACCAGACCAGAGGACTGGA GGGAGCTGGACTGCTGGGAGATAGTGAGGGACGAAGGGCAAAGGAAACCAGACCAGAGGACTGGA T C AGPAT1 Ensembl:ENSG00000204310 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:32176562..32176710 26863196 MeRIP-seq:(Medium) rs1337283861 Functional Loss SNV dbSNP153 33..33 33 - - - 75639 RMVar_ID_75639 Human_SNP_ID_272133580 m1A Human chr6 + 32178547 32178547 32178547 GCAGCAGCGGAGGAGGAGGACGGGGGCCCCGAAGGGCCAAATCGCGAGCGGGGCGGGGCGGGCGC GCAGCAGCGGAGGAGGAGGACGGGGGCCCCGAGGGGCCAAATCGCGAGCGGGGCGGGGCGGGCGC A G RNF5 Ensembl:ENSG00000204308 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr6:32178401..32178648;chr6:32178401..32179950;chr6:32178421..32179383;chr6:32178402..32180125;chr6:32178436..32178600 26863196 MeRIP-seq:(Medium) rs775322952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792262,Human_RBP_ID_4905437,Human_RBP_ID_5122192,Human_RBP_ID_5151844,Human_RBP_ID_5327402,Human_RBP_ID_22460639 75640 RMVar_ID_75640 Human_SNP_ID_272133851 m1A Human chr6 + 32179579 32179579 32179579 ATGTCTTCATCAGGTGCGTACTCAGGAGATGAAGAGGGAAATGGGGAGGTCTGAGGAGCTGTAAG ATGTCTTCATCAGGTGCGTACTCAGGAGATGAGGAGGGAAATGGGGAGGTCTGAGGAGCTGTAAG A G RNF5 Ensembl:ENSG00000204308 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:32179576..32179665 26863196 MeRIP-seq:(Medium) rs1384729026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949362,Human_RBP_ID_5398093,Human_RBP_ID_19130695 Human_Splice_Rec_758524,Human_Splice_Rec_758534 75641 RMVar_ID_75641 Human_SNP_ID_272134093 m1A Human chr6 - 32180297 32180294 32180297 AGCTCAAATACTGAGCAGCCAAAAAAAGAAGAAGATGGCGAGAAACAGGAAGAGGGAATCCTGCC AGCTCAAATACTGAGCAGCCAAAAAAAGAAGA___TGGCGAGAAACAGGAAGAGGGAATCCTGCC ATCT A RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32180246..32180366 26863196 MeRIP-seq:(Medium) rs752683365 Functional Loss DEL dbSNP153 33..35 33 - - - 75642 RMVar_ID_75642 Human_SNP_ID_272135920 m1A Human chr6 + 32185963 32185963 32185963 GATTGGGCAGGGCTGGCGTCTCCACAGATTCCAGAGCATACAAGTGGGGTGGGGAAGGGAAAGTG GATTGGGCAGGGCTGGCGTCTCCACAGATTCCCGAGCATACAAGTGGGGTGGGGAAGGGAAAGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32185828..32185997 26863196 MeRIP-seq:(Medium) rs1209844026 Functional Loss SNV dbSNP153 33..33 33 - - - 75643 RMVar_ID_75643 Human_SNP_ID_272135976 m1A Human chr6 + 32186157 32186157 32186157 CTGTGTAAGAAAGAAAGCGAGAGAGGAAAAAGATGGAAAAAAGGGAGAGACAGACCCCACACTCC CTGTGTAAGAAAGAAAGCGAGAGAGGAAAAAGTTGGAAAAAAGGGAGAGACAGACCCCACACTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32186106..32186261 26863196 MeRIP-seq:(Medium) rs997 Functional Loss SNV dbSNP153 33..33 33 - - - 75644 RMVar_ID_75644 Human_SNP_ID_272136327 m1A Human chr6 - 32187308 32187308 32187308 TCCAAGAGGAGGCAAACATCTATGCTGTCAAGACCGCCGTGTCAGTCACCCAGGGGGGCCACAGC TCCAAGAGGAGGCAAACATCTATGCTGTCAAGCCCGCCGTGTCAGTCACCCAGGGGGGCCACAGC T G PBX2 Ensembl:ENSG00000204304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32187259..32187397 26863196 MeRIP-seq:(Medium) rs80169725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662094,Human_RBP_ID_792306,Human_RBP_ID_18195520,Human_RBP_ID_26353744 Human_Splice_Rec_758730,Human_Splice_Rec_758731,Human_Splice_Rec_758737,Human_Splice_Rec_758748,Human_Splice_Rec_758754 RMVar_hsa_circ_16339 75645 RMVar_ID_75645 Human_SNP_ID_272136625 m1A Human chr6 + 32188364 32188364 32188364 GATGGAGTTGTCAGGGGACACACCACCACCAGAGGCTGCAGCGGCTGCAGCTGCTGCTGCTGAGC GATGGAGTTGTCAGGGGACACACCACCACCAGCGGCTGCAGCGGCTGCAGCTGCTGCTGCTGAGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32188251..32188720 32194978 MeRIP-seq:(Medium) rs1561894019 Functional Loss SNV dbSNP153 33..33 33 - - - 75646 RMVar_ID_75646 Human_SNP_ID_272136916 m1A Human chr6 - 32189492 32189492 32189492 CACCCCCAGGCCCTGAAACCTTCACAGAGGGAACCCCCGGTGGCCCGGCTCCCCACTCCTAACCT CACCCCCAGGCCCTGAAACCTTCACAGAGGGAGCCCCCGGTGGCCCGGCTCCCCACTCCTAACCT T C PBX2 Ensembl:ENSG00000204304 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:32189445..32189538 26863196 MeRIP-seq:(Medium) rs1486915309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134120,Human_RBP_ID_17090852 75647 RMVar_ID_75647 Human_SNP_ID_272136979 m1A Human chr6 + 32189785 32189752 32189785 CCCCGATGTCTTGCTTCCCTCGGCCTCCCGGGACCCCCCCGCTACCCCCACCGGGGTCTCCGCCA _________________________________CCCCCCCGCTACCCCCACCGGGGTCTCCGCCA TCCCCGATGTCTTGCTTCCCTCGGCCTCCCGGGA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:32189726..32190100;chr6:32189726..32190061;chr6:32189709..32190036 26863196 MeRIP-seq:(Medium) rs1561895904 Functional Loss DEL dbSNP153 1..33 33 - - - 75648 RMVar_ID_75648 Human_SNP_ID_272137432 m1A Human chr6 - 32191352 32191351 32191353 CCCCACACACACCTGCTGAGACTTGAGCCCCAACCAGCCCTTCCTTGCCACTGGTCTCAAAGCTG CCCCACACACACCTGCTGAGACTTGAGCCCC__CCAGCCCTTCCTTGCCACTGGTCTCAAAGCTG GTT G GPSM3 Ensembl:ENSG00000213654 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32191301..32191497 32194978 MeRIP-seq:(Medium) rs1561899780 Functional Loss DEL dbSNP153 32..33 33 - - - 75649 RMVar_ID_75649 Human_SNP_ID_272137433 m1A Human chr6 - 32191352 32191352 32191352 CCCCACACACACCTGCTGAGACTTGAGCCCCAACCAGCCCTTCCTTGCCACTGGTCTCAAAGCTG CCCCACACACACCTGCTGAGACTTGAGCCCCAGCCAGCCCTTCCTTGCCACTGGTCTCAAAGCTG T C GPSM3 Ensembl:ENSG00000213654 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32191301..32191497 32194978 MeRIP-seq:(Medium) rs926426857 Functional Loss SNV dbSNP153 33..33 33 - - - 75650 RMVar_ID_75650 Human_SNP_ID_272326436 m1A Human chr6 - 32838687 32838681 32838687 GAGAGACGGAGCGGACCTCAGCGCTGAAGCAGAAGTCCCCGGAGCTGCGGTCTCCCCGCCGCGGC GAGAGACGGAGCGGACCTCAGCGCTGAAGCAG______CCGGAGCTGCGGTCTCCCCGCCGCGGC GGGACTT G TAP2,AL669918.1 Ensembl:ENSG00000204267,Ensembl:ENSG00000250264 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32838657..32838775 26863196 MeRIP-seq:(Medium) rs1303664106 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_792303,Human_RBP_ID_4903251,Human_RBP_ID_22461211 Human_Splice_Rec_759679,Human_Splice_Rec_759707,Human_Splice_Rec_759729,Human_Splice_Rec_759751 75651 RMVar_ID_75651 Human_SNP_ID_272327432 m1A Human chr6 - 32842756 32842756 32842756 TCCAGGTGCCTTACGGGTGAACAAGGTGATTGAGATTAACCCTTACCTGCTTGGCACCATGTCTG TCCAGGTGCCTTACGGGTGAACAAGGTGATTGTGATTAACCCTTACCTGCTTGGCACCATGTCTG T A PSMB8 Ensembl:ENSG00000204264 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32842676..32842832 32194978 MeRIP-seq:(Medium) rs779346709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759787,Human_Splice_Rec_759796,Human_Splice_Rec_759797,Human_Splice_Rec_759806,Human_Splice_Rec_759807,Human_Splice_Rec_759814,Human_Splice_Rec_759815,Human_Splice_Rec_759823 Human_miRNA_ID_613575,Human_miRNA_ID_616914 75652 RMVar_ID_75652 Human_SNP_ID_272327760 m1A Human chr6 + 32843893 32843893 32843893 GGGGTAAAGCGAGCTCTGGAGATCGCATAGAGAAACTGTAGTGTCCTGGGTCCGAGCGACGCCCG GGGGTAAAGCGAGCTCTGGAGATCGCATAGAGGAACTGTAGTGTCCTGGGTCCGAGCGACGCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32843827..32843985 26863196 MeRIP-seq:(Medium) rs374038167 Functional Loss SNV dbSNP153 33..33 33 - - - 75653 RMVar_ID_75653 Human_SNP_ID_272327924 m1A Human chr6 + 32844339 32844339 32844339 GGGGTGGGTAGGGTCGTGTCATCTAAAGGCGCAGCTTCAACCAGAAGACTAGAAGTCAGCCAGGA GGGGTGGGTAGGGTCGTGTCATCTAAAGGCGCCGCTTCAACCAGAAGACTAGAAGTCAGCCAGGA A C PSMB8-AS1,PSMB9 Ensembl:ENSG00000204261,Ensembl:ENSG00000240065 lincRNA,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32844135..32856227 26863196 MeRIP-seq:(Medium) rs980080102 Functional Loss SNV dbSNP153 33..33 33 - - - 75654 RMVar_ID_75654 Human_SNP_ID_272327933 m1A Human chr6 + 32844371 32844371 32844371 AGCTTCAACCAGAAGACTAGAAGTCAGCCAGGAGCTGGGAGTAGTGTCACGCGGGGTGGGGGTTC AGCTTCAACCAGAAGACTAGAAGTCAGCCAGGGGCTGGGAGTAGTGTCACGCGGGGTGGGGGTTC A G PSMB8-AS1,PSMB9 Ensembl:ENSG00000204261,Ensembl:ENSG00000240065 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32844322..32844414 26863196 MeRIP-seq:(Medium) rs972405189 Functional Loss SNV dbSNP153 33..33 33 - - - 75655 RMVar_ID_75655 Human_SNP_ID_272329666 m1A Human chr6 - 32851039 32851039 32851039 GGTACCTGGTGCGAGGCCTATGTCTCTTGGGGATCATGCTCTGGGGATCAGTGTCCCTCACCATG GGTACCTGGTGCGAGGCCTATGTCTCTTGGGGTTCATGCTCTGGGGATCAGTGTCCCTCACCATG T A TAP1 Ensembl:ENSG00000168394 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32850991..32851141 32194978 MeRIP-seq:(Medium) rs748668600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759901,Human_Splice_Rec_759929,Human_Splice_Rec_759949 RMVar_hsa_circ_115915,RMVar_hsa_circ_105671,RMVar_hsa_circ_237850,RMVar_hsa_circ_237851 75656 RMVar_ID_75656 Human_SNP_ID_272329667 m1A Human chr6 - 32851039 32851039 32851039 GGTACCTGGTGCGAGGCCTATGTCTCTTGGGGATCATGCTCTGGGGATCAGTGTCCCTCACCATG GGTACCTGGTGCGAGGCCTATGTCTCTTGGGGCTCATGCTCTGGGGATCAGTGTCCCTCACCATG T G TAP1 Ensembl:ENSG00000168394 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32850991..32851141 32194978 MeRIP-seq:(Medium) rs748668600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759901,Human_Splice_Rec_759929,Human_Splice_Rec_759949 RMVar_hsa_circ_115915,RMVar_hsa_circ_105671,RMVar_hsa_circ_237850,RMVar_hsa_circ_237851 75657 RMVar_ID_75657 Human_SNP_ID_272330329 m1A Human chr6 + 32853282 32853282 32853282 CCTGGTGCTATCCGCGGACCCGGGGGCTCCCCATGAGATCAGCTCTCGGAACAAGGCAAGTCCCG CCTGGTGCTATCCGCGGACCCGGGGGCTCCCCGTGAGATCAGCTCTCGGAACAAGGCAAGTCCCG A G PSMB9 Ensembl:ENSG00000240065 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32853231..32853331 32194978 MeRIP-seq:(Medium) rs763585575 Functional Loss SNV dbSNP153 33..33 33 - - - 75658 RMVar_ID_75658 Human_SNP_ID_272330755 m1A Human chr6 - 32854291 32854291 32854291 CCCCTCTGCCAACCCTCAAGCCCAGACCCATTACCCCGGTGTGGACTTCTCCCGCCCGGGGTAAG CCCCTCTGCCAACCCTCAAGCCCAGACCCATTTCCCCGGTGTGGACTTCTCCCGCCCGGGGTAAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32854221..32856227 32194978 MeRIP-seq:(Medium) rs78194576 Functional Loss SNV dbSNP153 33..33 33 - - - 75659 RMVar_ID_75659 Human_SNP_ID_272330756 m1A Human chr6 - 32854291 32854291 32854291 CCCCTCTGCCAACCCTCAAGCCCAGACCCATTACCCCGGTGTGGACTTCTCCCGCCCGGGGTAAG CCCCTCTGCCAACCCTCAAGCCCAGACCCATTGCCCCGGTGTGGACTTCTCCCGCCCGGGGTAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:32854221..32856227 32194978 MeRIP-seq:(Medium) rs78194576 Functional Loss SNV dbSNP153 33..33 33 - - - 75660 RMVar_ID_75660 Human_SNP_ID_272352242 m1A Human chr6 + 32953059 32953059 32953059 CATGACCCATACCTTCTTGCCACACAGTAGGTAGGAGCTACCAACCCAGCCAACCCAGCTTCCCC CATGACCCATACCTTCTTGCCACACAGTAGGTGGGAGCTACCAACCCAGCCAACCCAGCTTCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32952987..32953078 26863196 MeRIP-seq:(Medium) rs1317470940 Functional Loss SNV dbSNP153 33..33 33 - - - 75661 RMVar_ID_75661 Human_SNP_ID_272355576 m1A Human chr6 - 32968664 32968664 32968664 TGCTTGTCCATATCCCCAGCTTCCTATCCCGCAGTCCTGGACTCTGTCCCCCCCACTCGCCTCTC TGCTTGTCCATATCCCCAGCTTCCTATCCCGCGGTCCTGGACTCTGTCCCCCCCACTCGCCTCTC T C HLA-DMA Ensembl:ENSG00000204257 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32968615..32968790 26863196 MeRIP-seq:(Medium) rs9276935 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9127,GWAS_ID_9128,GWAS_ID_9129,GWAS_ID_9130,GWAS_ID_9131,GWAS_ID_9132,GWAS_ID_9133,GWAS_ID_9134,GWAS_ID_9135,GWAS_ID_9136,GWAS_ID_9137,GWAS_ID_9138,GWAS_ID_9139,GWAS_ID_9140,GWAS_ID_9141,GWAS_ID_9142,GWAS_ID_9143,GWAS_ID_9144,GWAS_ID_9145,GWAS_ID_9146,GWAS_ID_9147,GWAS_ID_9148,GWAS_ID_9149,GWAS_ID_9150,GWAS_ID_9151,GWAS_ID_9152,GWAS_ID_9153,GWAS_ID_9154,GWAS_ID_9155,GWAS_ID_9156,GWAS_ID_9157,GWAS_ID_9158,GWAS_ID_9159,GWAS_ID_9160,GWAS_ID_9161,GWAS_ID_9162,GWAS_ID_9163,GWAS_ID_9164,GWAS_ID_9165,GWAS_ID_9166,GWAS_ID_9167,GWAS_ID_9168,GWAS_ID_9169,GWAS_ID_9170,GWAS_ID_9171,GWAS_ID_9172,GWAS_ID_9173,GWAS_ID_9174,GWAS_ID_9175,GWAS_ID_9176,GWAS_ID_9177,GWAS_ID_9178,GWAS_ID_9179,GWAS_ID_9180,GWAS_ID_9181,GWAS_ID_9182 75662 RMVar_ID_75662 Human_SNP_ID_272355580 m1A Human chr6 + 32968670 32968669 32968670 CGAGTGGGGGGGACAGAGTCCAGGACTGCGGGATAGGAAGCTGGGGATATGGACAAGCAGCAGCG CGAGTGGGGGGGACAGAGTCCAGGACTGCGGG_TAGGAAGCTGGGGATATGGACAAGCAGCAGCG GA G BRD2 Ensembl:ENSG00000204256 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32968619..32968782 26863196 MeRIP-seq:(Medium) rs1445356961 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5511498,Human_RBP_ID_7593894,Human_RBP_ID_15790593,Human_RBP_ID_18450250,Human_RBP_ID_23060707 75663 RMVar_ID_75663 Human_SNP_ID_272355858 m1A Human chr6 - 32969300 32969300 32969300 CCCCAGGGGACGAATGGAATAGGGGGGGCCACACCGCCCCCTAACCCCTTTGCCCTCCAATGGGT CCCCAGGGGACGAATGGAATAGGGGGGGCCACGCCGCCCCCTAACCCCTTTGCCCTCCAATGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32969262..32969457 26863196 MeRIP-seq:(Medium) rs1165586833 Functional Loss SNV dbSNP153 33..33 33 - - - 75664 RMVar_ID_75664 Human_SNP_ID_272356783 m1A Human chr6 + 32971896 32971896 32971896 ACCACCCTCTTTCCCTGGAGTCGGCGGACCACAGCTCAGCCAATTGGCTTGGAGATGTGGCGGGT ACCACCCTCTTTCCCTGGAGTCGGCGGACCACGGCTCAGCCAATTGGCTTGGAGATGTGGCGGGT A G BRD2 Ensembl:ENSG00000204256 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32971757..32971908 32194978 MeRIP-seq:(Medium) rs1202638639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662287,Human_RBP_ID_1671444,Human_RBP_ID_8642751,Human_RBP_ID_9193633,Human_RBP_ID_15790653,Human_RBP_ID_22104933,Human_RBP_ID_23120278,Human_RBP_ID_27523773 RMVar_hsa_circ_34414,RMVar_hsa_circ_122764,RMVar_hsa_circ_237852 75665 RMVar_ID_75665 Human_SNP_ID_272357429 m1A Human chr6 - 32972884 32972884 32972884 AGTCACGTTTTGCAGCATCTTGACCGCAAGGAACCGGCGCTGCCCTCAGCCGCGGAAAGTCCGGG AGTCACGTTTTGCAGCATCTTGACCGCAAGGATCCGGCGCTGCCCTCAGCCGCGGAAAGTCCGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32972617..32973097 26863196 MeRIP-seq:(Medium) rs769381730 Functional Loss SNV dbSNP153 33..33 33 - - - 75666 RMVar_ID_75666 Human_SNP_ID_272358166 m1A Human chr6 + 32974534 32974534 32974534 CCAGAAGCAGCAGCACCAGGGAAGAGGATTCGAAAACCCTCTCTCTTGTATGAGGGCTTTGAGAG CCAGAAGCAGCAGCACCAGGGAAGAGGATTCGGAAACCCTCTCTCTTGTATGAGGGCTTTGAGAG A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs763014373 Functional Loss SNV dbSNP153 33..33 33 - - - 75667 RMVar_ID_75667 Human_SNP_ID_272358176 m1A Human chr6 + 32974551 32974551 32974551 AGGGAAGAGGATTCGAAAACCCTCTCTCTTGTATGAGGGCTTTGAGAGCCCCACAATGGCTTCGG AGGGAAGAGGATTCGAAAACCCTCTCTCTTGTGTGAGGGCTTTGAGAGCCCCACAATGGCTTCGG A G BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32974501..32974550 32194978 MeRIP-seq:(Medium) rs200307380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671475,Human_RBP_ID_4883810,Human_RBP_ID_8642772,Human_RBP_ID_18074202,Human_RBP_ID_18863546,Human_RBP_ID_22103264,Human_RBP_ID_22311644,Human_RBP_ID_22831439,Human_RBP_ID_27096693 Human_Splice_Rec_760054,Human_Splice_Rec_760078,Human_Splice_Rec_760094,Human_Splice_Rec_760120,Human_Splice_Rec_760138,Human_Splice_Rec_760162,Human_Splice_Rec_760178,Human_Splice_Rec_760200,Human_Splice_Rec_760222 Human_miRNA_ID_756865,Human_miRNA_ID_1179390,Human_miRNA_ID_2309112,Human_miRNA_ID_2563450,Human_miRNA_ID_2710894,Human_miRNA_ID_2871140 RMVar_hsa_circ_122764,RMVar_hsa_circ_46967,RMVar_hsa_circ_237852 75668 RMVar_ID_75668 Human_SNP_ID_272358960 m1A Human chr6 + 32976140 32976140 32976140 AGAACAAGAGCTGGTAGTGACCATCCCTAAGAACAGCCACAAGAAGGGGGCCAAGTTGGCAGGTA AGAACAAGAGCTGGTAGTGACCATCCCTAAGACCAGCCACAAGAAGGGGGCCAAGTTGGCAGGTA A C BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32976090..32976191 26863196 MeRIP-seq:(Medium) rs772469309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81969,Human_RBP_ID_949377,Human_RBP_ID_2019003,Human_RBP_ID_3806739,Human_RBP_ID_3969918,Human_RBP_ID_5398734,Human_RBP_ID_7594020,Human_RBP_ID_8900445,Human_RBP_ID_9400345,Human_RBP_ID_15790802,Human_RBP_ID_18863562,Human_RBP_ID_19018290,Human_RBP_ID_19130717,Human_RBP_ID_22683975,Human_RBP_ID_23069057,Human_RBP_ID_26353174 Human_Splice_Rec_760059,Human_Splice_Rec_760083,Human_Splice_Rec_760099,Human_Splice_Rec_760125,Human_Splice_Rec_760145,Human_Splice_Rec_760167,Human_Splice_Rec_760183,Human_Splice_Rec_760205,Human_Splice_Rec_760227,Human_Splice_Rec_760243 75669 RMVar_ID_75669 Human_SNP_ID_272359187 m1A Human chr6 + 32976609 32976609 32976609 CGGAAAGCAGATACTACCACCCCTACACCTACAGCCATCTTGGCTCCTGGTTCTCCAGCTAGCCC CGGAAAGCAGATACTACCACCCCTACACCTACGGCCATCTTGGCTCCTGGTTCTCCAGCTAGCCC A G BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:32976422..32976684 26863196 MeRIP-seq:(Medium) rs1307603309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671508,Human_RBP_ID_2019008,Human_RBP_ID_4912415,Human_RBP_ID_7594036,Human_RBP_ID_8642784,Human_RBP_ID_9308291,Human_RBP_ID_9400346,Human_RBP_ID_17306696,Human_RBP_ID_17419773,Human_RBP_ID_17535747,Human_RBP_ID_18074225,Human_RBP_ID_18539079,Human_RBP_ID_18863566,Human_RBP_ID_22831456,Human_RBP_ID_27096716,Human_RBP_ID_27346056,Human_RBP_ID_27523822 Human_Splice_Rec_760062,Human_Splice_Rec_760086,Human_Splice_Rec_760102,Human_Splice_Rec_760128,Human_Splice_Rec_760148,Human_Splice_Rec_760170,Human_Splice_Rec_760186,Human_Splice_Rec_760208,Human_Splice_Rec_760230,Human_Splice_Rec_760246,Human_Splice_Rec_760252 Human_miRNA_ID_724916,Human_miRNA_ID_833463 75670 RMVar_ID_75670 Human_SNP_ID_272359248 m1A Human chr6 - 32976707 32976707 32976707 GAGAGTCAGGCAAGTCTTTGCGTGGGGGCTTGATGGGGCGACCACTCTCTCTACGCATAGGGGGA GAGAGTCAGGCAAGTCTTTGCGTGGGGGCTTGGTGGGGCGACCACTCTCTCTACGCATAGGGGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32976560..32976934 26863196 MeRIP-seq:(Medium) rs777728830 Functional Loss SNV dbSNP153 33..33 33 - - - 75671 RMVar_ID_75671 Human_SNP_ID_272359763 m1A Human chr6 - 32977978 32977978 32977978 AATACCTGTTCCTGTAGTTCTGCTAAGCGATGAGCCCTTTCTTCCTCTGAGTCTGAGCTTTCACT AATACCTGTTCCTGTAGTTCTGCTAAGCGATGGGCCCTTTCTTCCTCTGAGTCTGAGCTTTCACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:32977875..32978025;chr6:32977853..32978025 26863196 MeRIP-seq:(Medium) rs141740031 Functional Loss SNV dbSNP153 33..33 33 - - - 75672 RMVar_ID_75672 Human_SNP_ID_272359900 m1A Human chr6 + 32978189 32978189 32978189 TGTCCCAGGGTCCAATATCCAAGCCCAAGAGGAAAAGAGAGAAAAAAGAGAAAAAGAAGAAACGG TGTCCCAGGGTCCAATATCCAAGCCCAAGAGGCAAAGAGAGAAAAAAGAGAAAAAGAAGAAACGG A C BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1227448507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13414,Human_RBP_ID_2019025,Human_RBP_ID_3806758,Human_RBP_ID_3969929,Human_RBP_ID_4912435,Human_RBP_ID_9400350,Human_RBP_ID_18195522,Human_RBP_ID_18413780,Human_RBP_ID_18450264,Human_RBP_ID_19018293,Human_RBP_ID_22831465,Human_RBP_ID_23060834,Human_RBP_ID_24548563,Human_RBP_ID_26039192,Human_RBP_ID_26353758,Human_RBP_ID_27827527 Human_Splice_Rec_760068,Human_Splice_Rec_760108,Human_Splice_Rec_760134,Human_Splice_Rec_760154,Human_Splice_Rec_760176,Human_Splice_Rec_760192,Human_Splice_Rec_760214,Human_Splice_Rec_760236,Human_Splice_Rec_760250,Human_Splice_Rec_760260 75673 RMVar_ID_75673 Human_SNP_ID_272359954 m1A Human chr6 + 32978290 32978290 32978290 GAAGATGACAAGGGGCCTAGGGCACCCCGCCCACCTCAACCTAAGAAGTCCAAGAAAGCAAGTGG GAAGATGACAAGGGGCCTAGGGCACCCCGCCCGCCTCAACCTAAGAAGTCCAAGAAAGCAAGTGG A G BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:32978126..32978333 26863196 MeRIP-seq:(Medium) rs1262238028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2019026,Human_RBP_ID_3969929,Human_RBP_ID_5122613,Human_RBP_ID_7594096,Human_RBP_ID_8270139,Human_RBP_ID_8642803,Human_RBP_ID_9400351,Human_RBP_ID_18074241,Human_RBP_ID_19018293,Human_RBP_ID_23116504,Human_RBP_ID_24548384,Human_RBP_ID_26353758,Human_RBP_ID_27096744,Human_RBP_ID_27827528 Human_Splice_Rec_760069,Human_Splice_Rec_760109,Human_Splice_Rec_760155,Human_Splice_Rec_760193,Human_Splice_Rec_760215,Human_Splice_Rec_760237 Human_miRNA_ID_1271679 75674 RMVar_ID_75674 Human_SNP_ID_272359955 m1A Human chr6 + 32978296 32978293 32978296 GACAAGGGGCCTAGGGCACCCCGCCCACCTCAACCTAAGAAGTCCAAGAAAGCAAGTGGCAGTGG GACAAGGGGCCTAGGGCACCCCGCCCACCT___CCTAAGAAGTCCAAGAAAGCAAGTGGCAGTGG TCAA T BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32978126..32978400 26863196 MeRIP-seq:(Medium) rs1448510588 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_2019027,Human_RBP_ID_3969929,Human_RBP_ID_8270139,Human_RBP_ID_8642803,Human_RBP_ID_9400351,Human_RBP_ID_18074241,Human_RBP_ID_19018293,Human_RBP_ID_23116504,Human_RBP_ID_24548384,Human_RBP_ID_26353758,Human_RBP_ID_27096744,Human_RBP_ID_27827528 Human_Splice_Rec_760069,Human_Splice_Rec_760109,Human_Splice_Rec_760155,Human_Splice_Rec_760193,Human_Splice_Rec_760215,Human_Splice_Rec_760237 Human_miRNA_ID_1271679 75675 RMVar_ID_75675 Human_SNP_ID_272359956 m1A Human chr6 + 32978296 32978296 32978296 GACAAGGGGCCTAGGGCACCCCGCCCACCTCAACCTAAGAAGTCCAAGAAAGCAAGTGGCAGTGG GACAAGGGGCCTAGGGCACCCCGCCCACCTCACCCTAAGAAGTCCAAGAAAGCAAGTGGCAGTGG A C BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32978126..32978400 26863196 MeRIP-seq:(Medium) rs1469294501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2019027,Human_RBP_ID_3969929,Human_RBP_ID_8270139,Human_RBP_ID_8642803,Human_RBP_ID_9400351,Human_RBP_ID_18074241,Human_RBP_ID_19018293,Human_RBP_ID_23116504,Human_RBP_ID_24548384,Human_RBP_ID_26353758,Human_RBP_ID_27096744,Human_RBP_ID_27827528 Human_Splice_Rec_760069,Human_Splice_Rec_760109,Human_Splice_Rec_760155,Human_Splice_Rec_760193,Human_Splice_Rec_760215,Human_Splice_Rec_760237 Human_miRNA_ID_1271679 75676 RMVar_ID_75676 Human_SNP_ID_272360853 m1A Human chr6 + 32980450 32980450 32980450 AGATGTCAGCGGACAGCTCAATTCTACTAAAAAGCCCCCCAAGAAAGGTGAGTATATACTTTCAT AGATGTCAGCGGACAGCTCAATTCTACTAAAACGCCCCCCAAGAAAGGTGAGTATATACTTTCAT A C BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:32980426..32980450 26863196 MeRIP-seq:(Medium) rs772676674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1047065,Human_RBP_ID_1327028,Human_RBP_ID_1671560,Human_RBP_ID_2019049,Human_RBP_ID_3969933,Human_RBP_ID_7594177,Human_RBP_ID_8642817,Human_RBP_ID_8900501,Human_RBP_ID_9308303,Human_RBP_ID_9400356,Human_RBP_ID_15791044,Human_RBP_ID_17419782,Human_RBP_ID_17710593,Human_RBP_ID_18074255,Human_RBP_ID_18170956,Human_RBP_ID_18370366,Human_RBP_ID_18450268,Human_RBP_ID_18539080,Human_RBP_ID_27755046 Human_Splice_Rec_760073,Human_Splice_Rec_760113,Human_Splice_Rec_760159,Human_Splice_Rec_760197,Human_Splice_Rec_760219,Human_Splice_Rec_760241,Human_Splice_Rec_760261,Human_Splice_Rec_760265 75677 RMVar_ID_75677 Human_SNP_ID_272360864 m1A Human chr6 - 32980466 32980466 32980466 GTCAATCTGTAGTGGCATGAAAGTATATACTCACCTTTCTTGGGGGGCTTTTTAGTAGAATTGAG GTCAATCTGTAGTGGCATGAAAGTATATACTCGCCTTTCTTGGGGGGCTTTTTAGTAGAATTGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:32980368..32980474;chr6:32980451..32980475 26863196 MeRIP-seq:(Medium) rs765069285 Functional Loss SNV dbSNP153 33..33 33 - - - 75678 RMVar_ID_75678 Human_SNP_ID_272360946 m1A Human chr6 + 32980597 32980597 32980597 TCGAATTTGTTCTGCAGCGAATGAGAAAACAGAGTCATCCTCTGCACAGCAAGTAGCAGTGTCAC TCGAATTTGTTCTGCAGCGAATGAGAAAACAGGGTCATCCTCTGCACAGCAAGTAGCAGTGTCAC A G BRD2 Ensembl:ENSG00000204256 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs149549323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1113149,Human_RBP_ID_1671565,Human_RBP_ID_2019051,Human_RBP_ID_3968913,Human_RBP_ID_7594179,Human_RBP_ID_22831474,Human_RBP_ID_26355004,Human_RBP_ID_27096773 Human_Splice_Rec_760074,Human_Splice_Rec_760114,Human_Splice_Rec_760160,Human_Splice_Rec_760198,Human_Splice_Rec_760220,Human_Splice_Rec_760242,Human_Splice_Rec_760262,Human_Splice_Rec_760266 75679 RMVar_ID_75679 Human_SNP_ID_272360963 m1A Human chr6 - 32980626 32980626 32980626 ATCTGAGCTGGAGCTGGAAGCGCTAAGGCGTGACACTGCTACTTGCTGTGCAGAGGATGACTCTG ATCTGAGCTGGAGCTGGAAGCGCTAAGGCGTGGCACTGCTACTTGCTGTGCAGAGGATGACTCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:32980601..32980625 26863196 MeRIP-seq:(Medium) rs988496378 Functional Loss SNV dbSNP153 33..33 33 - - - 75680 RMVar_ID_75680 Human_SNP_ID_272360990 m1A Human chr6 - 32980674 32980674 32980674 TGAATCACTGGTGTCTGAAGACGACGACGAGGAAGAGGAGGAGCTGGAATCTGAGCTGGAGCTGG TGAATCACTGGTGTCTGAAGACGACGACGAGGGAGAGGAGGAGCTGGAATCTGAGCTGGAGCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32980625..32980851 26863196 MeRIP-seq:(Medium) rs1029981451 Functional Loss SNV dbSNP153 33..33 33 - - - 75681 RMVar_ID_75681 Human_SNP_ID_272361034 m1A Human chr6 + 32980743 32980743 32980743 CAGGCTAAGGGGTCAGGCCAGATGGGGCAGGAAGGCTCCGCAGGACCGGACCCCTAGACCACCCT CAGGCTAAGGGGTCAGGCCAGATGGGGCAGGACGGCTCCGCAGGACCGGACCCCTAGACCACCCT A C BRD2 Ensembl:ENSG00000204256 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32980576..32981106 26863196 MeRIP-seq:(Medium) rs1342449290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252491,Human_RBP_ID_1047068,Human_RBP_ID_2019052,Human_RBP_ID_5121928,Human_RBP_ID_7594185,Human_RBP_ID_18170957,Human_RBP_ID_18863607,Human_RBP_ID_26535653,Human_RBP_ID_27523846 75682 RMVar_ID_75682 Human_SNP_ID_272361139 m1A Human chr6 - 32980913 32980913 32980913 AGAGATCACTCCCCAATGGGGCTGGGAATTCAATGTTGTTTTGTCCATGTCCCTCCTTCAGTAAA AGAGATCACTCCCCAATGGGGCTGGGAATTCAGTGTTGTTTTGTCCATGTCCCTCCTTCAGTAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:32980735..32981186 26863196 MeRIP-seq:(Medium) rs1429640817 Functional Loss SNV dbSNP153 33..33 33 - - - 75683 RMVar_ID_75683 Human_SNP_ID_272408469 m1A Human chr6 + 33172302 33172302 33172302 GTCTGGGAGTCACACTCACAGCAGTGCCTGGGAGGCCTCTCTCTCCTGGGAATCCCCTCAGACCA GTCTGGGAGTCACACTCACAGCAGTGCCTGGGCGGCCTCTCTCTCCTGGGAATCCCCTCAGACCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33172295..33172378 26863196 MeRIP-seq:(Medium) rs984755949 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9183 75684 RMVar_ID_75684 Human_SNP_ID_272409637 m1A Human chr6 + 33175977 33175977 33175977 GGTGCTTGGCGTCTCCAGAGTGGAGGCTCAGTAGAACACGGAATTGGGGCCAGTGTGGGGTCTCT GGTGCTTGGCGTCTCCAGAGTGGAGGCTCAGTGGAACACGGAATTGGGGCCAGTGTGGGGTCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33175971..33176064 26863196 MeRIP-seq:(Medium) rs1430006502 Functional Loss SNV dbSNP153 33..33 33 - - - 75685 RMVar_ID_75685 Human_SNP_ID_272415310 m1A Human chr6 + 33197735 33197735 33197735 GAGTGGGATAAGGGAGAAGGGCATGTGGTCTAAGACGCCTGGGCAGGGCGGGTCCTTACCCTCCC GAGTGGGATAAGGGAGAAGGGCATGTGGTCTACGACGCCTGGGCAGGGCGGGTCCTTACCCTCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33197733..33197850 26863196 MeRIP-seq:(Medium) rs1282267427 Functional Loss SNV dbSNP153 33..33 33 - - - 75686 RMVar_ID_75686 Human_SNP_ID_272415722 m1A Human chr6 - 33199180 33199180 33199180 CTCCAGCTCCCCCAGGATTCTCCGGGCCTGTCAGCAGCCCCCAGGTGAGAGGTTGTGACCAACTT CTCCAGCTCCCCCAGGATTCTCCGGGCCTGTCTGCAGCCCCCAGGTGAGAGGTTGTGACCAACTT T A RXRB Ensembl:ENSG00000204231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33199173..33199253 26863196 MeRIP-seq:(Medium) rs760342051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968922,Human_RBP_ID_5134122,Human_RBP_ID_17090854 Human_Splice_Rec_760791,Human_Splice_Rec_760809 75687 RMVar_ID_75687 Human_SNP_ID_272416125 m1A Human chr6 - 33200339 33200336 33200339 TGGCGGCGGCGACGGCCCTGGCTGGATCCCGCAGCGGCGGCGGCGGCGGCGGTGGCAGGCGGAGA TGGCGGCGGCGACGGCCCTGGCTGGATCCCGC___GGCGGCGGCGGCGGCGGTGGCAGGCGGAGA CGCT C RXRB Ensembl:ENSG00000204231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:33199122..33200425;chr6:33200226..33200425;chr6:33199319..33200626;chr6:33199316..33200539 26863196 MeRIP-seq:(Medium) rs1449364226 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3968923,Human_RBP_ID_19016834,Human_RBP_ID_22461215 Human_Splice_Rec_760789,Human_Splice_Rec_760807,Human_Splice_Rec_760825 75688 RMVar_ID_75688 Human_SNP_ID_272416127 m1A Human chr6 - 33200339 33200339 33200339 TGGCGGCGGCGACGGCCCTGGCTGGATCCCGCAGCGGCGGCGGCGGCGGCGGTGGCAGGCGGAGA TGGCGGCGGCGACGGCCCTGGCTGGATCCCGCGGCGGCGGCGGCGGCGGCGGTGGCAGGCGGAGA T C RXRB Ensembl:ENSG00000204231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:33199122..33200425;chr6:33200226..33200425;chr6:33199319..33200626;chr6:33199316..33200539 26863196 MeRIP-seq:(Medium) rs895096120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968923,Human_RBP_ID_19016834,Human_RBP_ID_22461215 Human_Splice_Rec_760789,Human_Splice_Rec_760807,Human_Splice_Rec_760825 75689 RMVar_ID_75689 Human_SNP_ID_272416132 m1A Human chr6 + 33200345 33200345 33200345 CCTGCCACCGCCGCCGCCGCCGCCGCTGCGGGATCCAGCCAGGGCCGTCGCCGCCGCCACCGGGA CCTGCCACCGCCGCCGCCGCCGCCGCTGCGGGGTCCAGCCAGGGCCGTCGCCGCCGCCACCGGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:33200326..33200350;chr6:33200226..33200400 26863196 MeRIP-seq:(Medium) rs781605443 Functional Loss SNV dbSNP153 33..33 33 - - - 75690 RMVar_ID_75690 Human_SNP_ID_272416133 m1A Human chr6 + 33200345 33200345 33200345 CCTGCCACCGCCGCCGCCGCCGCCGCTGCGGGATCCAGCCAGGGCCGTCGCCGCCGCCACCGGGA CCTGCCACCGCCGCCGCCGCCGCCGCTGCGGGTTCCAGCCAGGGCCGTCGCCGCCGCCACCGGGA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:33200326..33200350;chr6:33200226..33200400 26863196 MeRIP-seq:(Medium) rs781605443 Functional Loss SNV dbSNP153 33..33 33 - - - 75691 RMVar_ID_75691 Human_SNP_ID_272416653 m1A Human chr6 - 33201851 33201848 33201852 CATCTCCCAGGAGCCCACCGGAAGCAAAACTGAGCAAGATCTGAAGTAGAGAGCGATGCCGGGGA CATCTCCCAGGAGCCCACCGGAAGCAAAACT____AAGATCTGAAGTAGAGAGCGATGCCGGGGA TGCTC T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:33201801..33201875 26863196 MeRIP-seq:(Medium) rs1228261871 Functional Loss DEL dbSNP153 32..35 33 - - - 75692 RMVar_ID_75692 Human_SNP_ID_272416672 m1A Human chr6 - 33201915 33201915 33201915 GTTAGATTTGAGGTAGAAGTCAGAGGTTACTTACCAAGAGCATGAGGAATGAGGTGCAGGAAAGC GTTAGATTTGAGGTAGAAGTCAGAGGTTACTTTCCAAGAGCATGAGGAATGAGGTGCAGGAAAGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33201876..33201925 32194978 MeRIP-seq:(Medium) rs112161031 Functional Loss SNV dbSNP153 33..33 33 - - - 75693 RMVar_ID_75693 Human_SNP_ID_272416843 m1A Human chr6 + 33202383 33202383 33202383 AGGAGGACATGGTCACAGTCATGGACATGGACACGCTCACAGTCATACACGTGGAAGTCATGGAC AGGAGGACATGGTCACAGTCATGGACATGGACCCGCTCACAGTCATACACGTGGAAGTCATGGAC A C SLC39A7 Ensembl:ENSG00000112473 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33202333..33202440 26863196 MeRIP-seq:(Medium) rs754739126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662385,Human_RBP_ID_1671629,Human_RBP_ID_2019114,Human_RBP_ID_3806846,Human_RBP_ID_5617822,Human_RBP_ID_7594333,Human_RBP_ID_8900538,Human_RBP_ID_9193663,Human_RBP_ID_9400363,Human_RBP_ID_15791378,Human_RBP_ID_18084777,Human_RBP_ID_18863694,Human_RBP_ID_22772718,Human_RBP_ID_23067340 Human_Splice_Rec_760853,Human_Splice_Rec_760863,Human_Splice_Rec_760875,Human_Splice_Rec_760881 75694 RMVar_ID_75694 Human_SNP_ID_272416904 m1A Human chr6 + 33202610 33202608 33202610 AGCAGAGCTCAGAGGAAGAAGAAAAGGAAACAAGAGGGGTTCAGAAGAGGCGAGGAGGGAGCACA AGCAGAGCTCAGAGGAAGAAGAAAAGGAAAC__GAGGGGTTCAGAAGAGGCGAGGAGGGAGCACA CAA C SLC39A7 Ensembl:ENSG00000112473 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33202551..33202720 26863196 MeRIP-seq:(Medium) rs780681928 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_252074,Human_RBP_ID_1671634,Human_RBP_ID_3969939,Human_RBP_ID_8642892,Human_RBP_ID_9400366,Human_RBP_ID_18413848,Human_RBP_ID_19018300,Human_RBP_ID_22774034,Human_RBP_ID_23060938,Human_RBP_ID_24387685,Human_RBP_ID_24548387,Human_RBP_ID_26353773,Human_RBP_ID_27827533 Human_Splice_Rec_760854,Human_Splice_Rec_760864,Human_Splice_Rec_760865,Human_Splice_Rec_760876,Human_Splice_Rec_760877,Human_Splice_Rec_760882,Human_Splice_Rec_760883 75695 RMVar_ID_75695 Human_SNP_ID_272417269 m1A Human chr6 - 33203921 33203921 33203921 CCCTAATGCCAAAGTAACCATTCTCCCAGGCTACAGTTCCTTCCTTTGGCAGATGTCCCTGGCCA CCCTAATGCCAAAGTAACCATTCTCCCAGGCTGCAGTTCCTTCCTTTGGCAGATGTCCCTGGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33203870..33204145 26863196 MeRIP-seq:(Medium) rs1290637619 Functional Loss SNV dbSNP153 33..33 33 - - - 75696 RMVar_ID_75696 Human_SNP_ID_272417341 m1A Human chr6 - 33204250 33204250 33204250 GACACACGATTGATGTTTGATGTTTATCCCCGACTCCTCCTGTTACCCTCTCTGTCCAGGACTCT GACACACGATTGATGTTTGATGTTTATCCCCGGCTCCTCCTGTTACCCTCTCTGTCCAGGACTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33204201..33204250 26863196 MeRIP-seq:(Medium) rs1189314359 Functional Loss SNV dbSNP153 33..33 33 - - - 75697 RMVar_ID_75697 Human_SNP_ID_272417685 m1A Human chr6 - 33205063 33205052 33205064 GGCGGCCCTGGCCTCAGACACGTCAGCCTGGAAGGCAGCATGGTTCCCTCGGGGCGGCCCCTCCT GGCGGCCCTGGCCTCAGACACGTCAGCCTGG____________TTCCCTCGGGGCGGCCCCTCCT ACCATGCTGCCTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33204914..33205093 26863196 MeRIP-seq:(Medium) rs763890055 Functional Loss DEL dbSNP153 32..43 33 - - - 75698 RMVar_ID_75698 Human_SNP_ID_272418843 m1A Human chr6 + 33208845 33208845 33208845 CCCGGTCACCATGACGACGCCGGCGAATGCCCAGAATGCCAGCAAAACGTGGGAACTGAGTCTGT CCCGGTCACCATGACGACGCCGGCGAATGCCCGGAATGCCAGCAAAACGTGGGAACTGAGTCTGT A G RING1 Ensembl:ENSG00000204227 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33208744..33208924 26863196 MeRIP-seq:(Medium) rs1306895821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671655,Human_RBP_ID_2019130,Human_RBP_ID_3806855,Human_RBP_ID_9193668,Human_RBP_ID_18863704 Human_Splice_Rec_760916,Human_Splice_Rec_760917 75699 RMVar_ID_75699 Human_SNP_ID_272419061 m1A Human chr6 + 33209597 33209597 33209597 CTGTTTCTAAAACCCCTTTCCCTCTAACCCACACCACCTTTCTACTCACTGATGCCTTCAGGAAG CTGTTTCTAAAACCCCTTTCCCTCTAACCCACGCCACCTTTCTACTCACTGATGCCTTCAGGAAG A G RING1 Ensembl:ENSG00000204227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33209595..33209814 26863196 MeRIP-seq:(Medium) rs1297234966 Functional Loss SNV dbSNP153 33..33 33 - - - 75700 RMVar_ID_75700 Human_SNP_ID_272419477 m1A Human chr6 + 33211239 33211239 33211239 ATGAGTGGGGGGGAAGGAGAGCCCGGGGAGGGAGAAGGGGATGGAGAAGATGTGAGCTCAGACTC ATGAGTGGGGGGGAAGGAGAGCCCGGGGAGGGGGAAGGGGATGGAGAAGATGTGAGCTCAGACTC A G RING1 Ensembl:ENSG00000204227 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33211137..33211570 26863196 MeRIP-seq:(Medium) rs544269787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251774,Human_RBP_ID_841920,Human_RBP_ID_2019141,Human_RBP_ID_3968926,Human_RBP_ID_5151858,Human_RBP_ID_5400578,Human_RBP_ID_7594383,Human_RBP_ID_8215191,Human_RBP_ID_9437798,Human_RBP_ID_18957269,Human_RBP_ID_22683990,Human_RBP_ID_27842609 Human_Splice_Rec_760922,Human_Splice_Rec_760930 RMVar_hsa_circ_106652,RMVar_hsa_circ_237855 75701 RMVar_ID_75701 Human_SNP_ID_272419723 m1A Human chr6 - 33211897 33211897 33211897 GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCACCCCCACCCTCCCCGCCACACCCATCAGGTCC GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCTCCCCCACCCTCCCCGCCACACCCATCAGGTCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:33211851..33212000 26863196 MeRIP-seq:(Medium) rs754640364 Functional Loss SNV dbSNP153 33..33 33 - - - 75702 RMVar_ID_75702 Human_SNP_ID_272419724 m1A Human chr6 - 33211897 33211897 33211897 GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCACCCCCACCCTCCCCGCCACACCCATCAGGTCC GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCCCCCCCACCCTCCCCGCCACACCCATCAGGTCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:33211851..33212000 26863196 MeRIP-seq:(Medium) rs754640364 Functional Loss SNV dbSNP153 33..33 33 - - - 75703 RMVar_ID_75703 Human_SNP_ID_272419760 m1A Human chr6 + 33211965 33211965 33211965 GCCCAGCCTGGAGGGCGTCAGTGAAAAGCAGTACACCATCTACATCGCACCTGGAGGCGGGGCGT GCCCAGCCTGGAGGGCGTCAGTGAAAAGCAGTGCACCATCTACATCGCACCTGGAGGCGGGGCGT A G RING1 Ensembl:ENSG00000204227 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33211751..33211975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22104973,Human_RBP_ID_27523931 Human_Splice_Rec_760925,Human_Splice_Rec_760933 RMVar_hsa_circ_106652,RMVar_hsa_circ_237855 75704 RMVar_ID_75704 Human_SNP_ID_272419761 m1A Human chr6 + 33211965 33211965 33211965 GCCCAGCCTGGAGGGCGTCAGTGAAAAGCAGTACACCATCTACATCGCACCTGGAGGCGGGGCGT GCCCAGCCTGGAGGGCGTCAGTGAAAAGCAGTTCACCATCTACATCGCACCTGGAGGCGGGGCGT A T RING1 Ensembl:ENSG00000204227 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33211751..33211975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22104973,Human_RBP_ID_27523931 Human_Splice_Rec_760925,Human_Splice_Rec_760933 RMVar_hsa_circ_106652,RMVar_hsa_circ_237855 75705 RMVar_ID_75705 Human_SNP_ID_272419922 m1A Human chr6 + 33212393 33212393 33212393 CTGGAGCTGTGCTATGCTCCCACCAAGGATCCAAAGTGACCCCACCAGGGGACAGCCAGAGGAAG CTGGAGCTGTGCTATGCTCCCACCAAGGATCCGAAGTGACCCCACCAGGGGACAGCCAGAGGAAG A G RING1 Ensembl:ENSG00000204227 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33212344..33212500 26863196 MeRIP-seq:(Medium) rs953788385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790694,Human_RBP_ID_1671678 Human_Splice_Rec_760926,Human_Splice_Rec_760934 RMVar_hsa_circ_106652,RMVar_hsa_circ_237855 75706 RMVar_ID_75706 Human_SNP_ID_272433476 m1A Human chr6 + 33267236 33267234 33267236 TGCGCTGTGTGAGGCACCAGGATGGGGGCCTCAAGTTCAGTGGGGGAGATGACAGAGCCGCGGGT TGCGCTGTGTGAGGCACCAGGATGGGGGCCT__AGTTCAGTGGGGGAGATGACAGAGCCGCGGGT TCA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33267190..33267290 32194978 MeRIP-seq:(Medium) rs1177183091 Functional Loss DEL dbSNP153 32..33 33 - - - 75707 RMVar_ID_75707 Human_SNP_ID_272433863 m1A Human chr6 - 33268627 33268627 33268627 TGCTAACCAGGGCAATTCTGGAGGCTCCAGTGACAGAGCCCAGGTTCTTGGAGCAGCTACAGGAG TGCTAACCAGGGCAATTCTGGAGGCTCCAGTGGCAGAGCCCAGGTTCTTGGAGCAGCTACAGGAG T C VPS52 Ensembl:ENSG00000223501 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33268578..33268665 26863196 MeRIP-seq:(Medium) rs1222927390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285064,Human_RBP_ID_948657,Human_RBP_ID_9401964,Human_RBP_ID_19016850 Human_Splice_Rec_760980,Human_Splice_Rec_761016,Human_Splice_Rec_761050,Human_Splice_Rec_761122,Human_Splice_Rec_761138 75708 RMVar_ID_75708 Human_SNP_ID_272434747 m1A Human chr6 + 33271632 33271630 33271633 CCTCCTCCATATCTGAGGTCCCAGCCCGCAACACCAGTTCCCGGGCCGCAGCCGCCATGGTCGCA CCTCCTCCATATCTGAGGTCCCAGCCCGCAA___CAGTTCCCGGGCCGCAGCCGCCATGGTCGCA ACAC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33271595..33271845 26863196 MeRIP-seq:(Medium) rs1359812830 Functional Loss DEL dbSNP153 32..34 33 - - - 75709 RMVar_ID_75709 Human_SNP_ID_272434748 m1A Human chr6 + 33271632 33271632 33271632 CCTCCTCCATATCTGAGGTCCCAGCCCGCAACACCAGTTCCCGGGCCGCAGCCGCCATGGTCGCA CCTCCTCCATATCTGAGGTCCCAGCCCGCAACCCCAGTTCCCGGGCCGCAGCCGCCATGGTCGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33271595..33271845 26863196 MeRIP-seq:(Medium) rs749953122 Functional Loss SNV dbSNP153 33..33 33 - - - 75710 RMVar_ID_75710 Human_SNP_ID_272435000 m1A Human chr6 - 33272121 33272121 33272121 CGCTGGATCACGGCACGGATTCCAGTCTTACCATGGCTGCAGCACAAGCGGCGGCGTGTAGGCCT CGCTGGATCACGGCACGGATTCCAGTCTTACCTTGGCTGCAGCACAAGCGGCGGCGTGTAGGCCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33272076..33272125 26863196 MeRIP-seq:(Medium) rs746309014 Functional Loss SNV dbSNP153 33..33 33 - - - 75711 RMVar_ID_75711 Human_SNP_ID_272436132 m1A Human chr6 - 33275987 33275987 33275987 AGTCTGGGATCTTGTACTGGCGTGGATTCTGCATAATGGTGATCACACGTTCCACCTGGCAGGCA AGTCTGGGATCTTGTACTGGCGTGGATTCTGCGTAATGGTGATCACACGTTCCACCTGGCAGGCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:33275776..33276050 26863410 MeRIP-seq:(Medium) rs1416455071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15791969 75712 RMVar_ID_75712 Human_SNP_ID_272436142 m1A Human chr6 + 33276065 33276065 33276065 ACAGAAGGATGTAAAGGATGGAAAATACAGCCAGGTGTGTACTGAAATGAGGGCAGGATTAGAGG ACAGAAGGATGTAAAGGATGGAAAATACAGCCTGGTGTGTACTGAAATGAGGGCAGGATTAGAGG A T RPS18 Ensembl:ENSG00000231500 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33276055..33276173 26863196 MeRIP-seq:(Medium) rs61742768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790736,Human_RBP_ID_1671732,Human_RBP_ID_2019204,Human_RBP_ID_8642975,Human_RBP_ID_17663690,Human_RBP_ID_18084796,Human_RBP_ID_18195532,Human_RBP_ID_21902884,Human_RBP_ID_23061004,Human_RBP_ID_23214782,Human_RBP_ID_24158246,Human_RBP_ID_25999056,Human_RBP_ID_26828361 Human_Splice_Rec_761149,Human_Splice_Rec_761159,Human_Splice_Rec_761179,Human_Splice_Rec_761189,Human_Splice_Rec_761195,Human_Splice_Rec_761201 Human_miRNA_ID_2330943,Human_miRNA_ID_2428502,Human_miRNA_ID_2488301,Human_miRNA_ID_2964025 RMVar_hsa_circ_124415,RMVar_hsa_circ_237857 75713 RMVar_ID_75713 Human_SNP_ID_272436578 m1A Human chr6 - 33277260 33277260 33277260 AGCGCACCCTGGGGGGCGGGGAGAGGCGGTGCAGCTGCGGACCGCGGTCGAGGCATGCTGCGGGG AGCGCACCCTGGGGGGCGGGGAGAGGCGGTGCGGCTGCGGACCGCGGTCGAGGCATGCTGCGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33277210..33277310 26863196 MeRIP-seq:(Medium) rs577285236 Functional Loss SNV dbSNP153 33..33 33 - - - 75714 RMVar_ID_75714 Human_SNP_ID_272437387 m1A Human chr6 - 33279547 33279547 33279547 AGCCAAAGCCAAAGCAGAAGGGCCGCAGCTCCACGGCAAGCCTGGTGAAGAGGAAGAGGAAGGTC AGCCAAAGCCAAAGCAGAAGGGCCGCAGCTCCGCGGCAAGCCTGGTGAAGAGGAAGAGGAAGGTC T C WDR46 Ensembl:ENSG00000227057 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr6:33279458..33279564;chr6:33279476..33279550 26863196,32194978 MeRIP-seq:(Medium) rs1301050574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26355017 Human_Splice_Rec_761212,Human_Splice_Rec_761216,Human_Splice_Rec_761217,Human_Splice_Rec_761244,Human_Splice_Rec_761245,Human_Splice_Rec_761256 75715 RMVar_ID_75715 Human_SNP_ID_272440101 m1A Human chr6 - 33289012 33289012 33289012 CGTGAGTGCGGAGTTCCTGATGTGCCTGTAGAAACCGCGGCGATACTGGGAGGAAGAGACCGTTC CGTGAGTGCGGAGTTCCTGATGTGCCTGTAGAGACCGCGGCGATACTGGGAGGAAGAGACCGTTC T C WDR46 Ensembl:ENSG00000227057 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33288976..33289225 26863196 MeRIP-seq:(Medium) rs368603141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18450282 Human_Splice_Rec_761220,Human_Splice_Rec_761278,Human_Splice_Rec_761290 75716 RMVar_ID_75716 Human_SNP_ID_272440123 m1A Human chr6 + 33289057 33289057 33289057 TCAGGAACTCCGCACTCACGCCCCGCCCCCCGACCCCACAGCTAAAAACTTCGTTTCCCACCCAG TCAGGAACTCCGCACTCACGCCCCGCCCCCCGCCCCCACAGCTAAAAACTTCGTTTCCCACCCAG A C RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:33289026..33289075 26863196 MeRIP-seq:(Medium) rs774221772 Functional Loss SNV dbSNP153 33..33 33 - - - 75717 RMVar_ID_75717 Human_SNP_ID_272440176 m1A Human chr6 - 33289166 33289166 33289166 CACGTGGATCGCCGTTCGGGTGGGCGAGATGGAGACAGCCCCCAAGCCGGGCAAGGATGTCCCGC CACGTGGATCGCCGTTCGGGTGGGCGAGATGGGGACAGCCCCCAAGCCGGGCAAGGATGTCCCGC T C WDR46 Ensembl:ENSG00000227057 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33289008..33289225 26863196 MeRIP-seq:(Medium) rs773066068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791519,Human_RBP_ID_4903918,Human_RBP_ID_9400380,Human_RBP_ID_18413783,Human_RBP_ID_22104974,Human_RBP_ID_23214785 Human_Splice_Rec_761219,Human_Splice_Rec_761277,Human_Splice_Rec_761289 75718 RMVar_ID_75718 Human_SNP_ID_272440375 m1A Human chr6 + 33289817 33289817 33289817 GGAGCTCAGGTACCTTCCAGAGAGTGAGACCCAGCGCCCTTGTCTCGCACCCAGTAGGCTTTCAT GGAGCTCAGGTACCTTCCAGAGAGTGAGACCCGGCGCCCTTGTCTCGCACCCAGTAGGCTTTCAT A G PFDN6 Ensembl:ENSG00000204220 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:33289649..33289929 26863196 MeRIP-seq:(Medium) rs562808553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3969958,Human_RBP_ID_4884559,Human_RBP_ID_5121942,Human_RBP_ID_9336610,Human_RBP_ID_17663694,Human_RBP_ID_22460653,Human_RBP_ID_26355817 Human_Splice_Rec_761308,Human_Splice_Rec_761322,Human_Splice_Rec_761328,Human_Splice_Rec_761336 75719 RMVar_ID_75719 Human_SNP_ID_272440382 m1A Human chr6 - 33289829 33289829 33289829 GCCATGGCGGGGATGAAAGCCTACTGGGTGCGAGACAAGGGCGCTGGGTCTCACTCTCTGGAAGG GCCATGGCGGGGATGAAAGCCTACTGGGTGCGGGACAAGGGCGCTGGGTCTCACTCTCTGGAAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33289645..33290490 32194978 MeRIP-seq:(Medium) rs1254458211 Functional Loss SNV dbSNP153 33..33 33 - - - 75720 RMVar_ID_75720 Human_SNP_ID_272440477 m1A Human chr6 - 33290153 33290153 33290153 ATTTACTTAAGTCTGGGGATGAGAGGAAAGGCAATTTAGAAACATCAAATGTGCCACCTATCCCC ATTTACTTAAGTCTGGGGATGAGAGGAAAGGCGATTTAGAAACATCAAATGTGCCACCTATCCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:33290151..33290225 26863196 MeRIP-seq:(Medium) rs28362616 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 75721 RMVar_ID_75721 Human_SNP_ID_272440620 m1A Human chr6 - 33290688 33290684 33290688 GCTTACTAAGGAGAGACAAGGGAGACAAGCAGAAAGGGAGAAATTAGTAGGACTCACTATGGAGA GCTTACTAAGGAGAGACAAGGGAGACAAGCAG____GGAGAAATTAGTAGGACTCACTATGGAGA CCTTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33290686..33290785 32194978 MeRIP-seq:(Medium) rs1349521372 Functional Loss DEL dbSNP153 33..36 33 - - - 75722 RMVar_ID_75722 Human_SNP_ID_272440621 m1A Human chr6 - 33290690 33290690 33290690 TCGCTTACTAAGGAGAGACAAGGGAGACAAGCAGAAAGGGAGAAATTAGTAGGACTCACTATGGA TCGCTTACTAAGGAGAGACAAGGGAGACAAGCGGAAAGGGAGAAATTAGTAGGACTCACTATGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33290688..33290878 26863196 MeRIP-seq:(Medium) rs750218316 Functional Loss SNV dbSNP153 33..33 33 - - - 75723 RMVar_ID_75723 Human_SNP_ID_272440636 m1A Human chr6 - 33290737 33290737 33290737 CTCTGTTGCTCTGACTGCCGCTCAAGATCCCGAAGCTGGGATTCGTATCGCTTACTAAGGAGAGA CTCTGTTGCTCTGACTGCCGCTCAAGATCCCGGAGCTGGGATTCGTATCGCTTACTAAGGAGAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33290735..33290834 32194978 MeRIP-seq:(Medium) rs758616443 Functional Loss SNV dbSNP153 33..33 33 - - - 75724 RMVar_ID_75724 Human_SNP_ID_272441002 m1A Human chr6 - 33292162 33292162 33292162 TCTGCCTCAGGAACTCCTCCGAGTGAGGGAGGAGGGGGCTCCTTTCCCAGGATCAAGGCCACAGG TCTGCCTCAGGAACTCCTCCGAGTGAGGGAGGGGGGGGCTCCTTTCCCAGGATCAAGGCCACAGG T C RGL2 Ensembl:ENSG00000237441 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33292052..33292203 32194978 MeRIP-seq:(Medium) rs750533431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18171262 75725 RMVar_ID_75725 Human_SNP_ID_272442448 m1A Human chr6 + 33296727 33296727 33296727 GGGTATCCAGTAGGTGTCTGACCAGGGCCTCCAGAGTGCCAGCTCGGAGCCGTCGGGAGGAACGT GGGTATCCAGTAGGTGTCTGACCAGGGCCTCCGGAGTGCCAGCTCGGAGCCGTCGGGAGGAACGT A G PFDN6 Ensembl:ENSG00000204220 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33296676..33297171 32194978 MeRIP-seq:(Medium) rs1229862122 Functional Loss SNV dbSNP153 33..33 33 - - - 75726 RMVar_ID_75726 Human_SNP_ID_272443055 m1A Human chr6 + 33298879 33298879 33298879 GCGCAGGGTGCTCAGGCTCTGACCTGCTCGGGAGGGGTGGGGGCAGCGTGGGTCCTGAGCCGCTG GCGCAGGGTGCTCAGGCTCTGACCTGCTCGGGGGGGGTGGGGGCAGCGTGGGTCCTGAGCCGCTG A G RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33298867..33298967 26863196 MeRIP-seq:(Medium) rs1019321930 Functional Loss SNV dbSNP153 33..33 33 - - - 75727 RMVar_ID_75727 Human_SNP_ID_272443062 m1A Human chr6 - 33298912 33298912 33298912 GGGACTCGGTCCGGGGCCGGAGACCGACGGCAACAGCGGCTCAGGACCCACGCTGCCCCCACCCC GGGACTCGGTCCGGGGCCGGAGACCGACGGCAGCAGCGGCTCAGGACCCACGCTGCCCCCACCCC T C RGL2 Ensembl:ENSG00000237441 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33298871..33298968 26863196 MeRIP-seq:(Medium) rs1204823752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267206,Human_RBP_ID_3820769,Human_RBP_ID_5327415,Human_RBP_ID_21990759 Human_Splice_Rec_761409,Human_Splice_Rec_761441 75728 RMVar_ID_75728 Human_SNP_ID_272443337 m1A Human chr6 + 33299917 33299917 33299917 CAGACAGGCCAGTCCCTGTCCTCGAGGAGCCCATGATCCGCGGGGAGACAGGCATTTAACGACGA CAGACAGGCCAGTCCCTGTCCTCGAGGAGCCCTTGATCCGCGGGGAGACAGGCATTTAACGACGA A T RF00017-4596,lnc-PFDN6-3 RNACentral:URS0000934741,RNACentral:URS0000D5965F SRP RNA,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:33299901..33299925 26863196 MeRIP-seq:(Medium) rs1251911047 Functional Loss SNV dbSNP153 33..33 33 - - - 75729 RMVar_ID_75729 Human_SNP_ID_272443495 m1A Human chr6 - 33300512 33300509 33300513 GGACTACAGGGGCCCGCCACCACGCCCGGCTAACTTTTTGTGTTTTTAGTAGAGACGGGGTTTCA GGACTACAGGGGCCCGCCACCACGCCCGGCT____TTTTGTGTTTTTAGTAGAGACGGGGTTTCA AAGTT A TAPBP Ensembl:ENSG00000231925 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:33300501..33300550 26863196 MeRIP-seq:(Medium) rs936480627 Functional Loss DEL dbSNP153 32..35 33 - - - 75730 RMVar_ID_75730 Human_SNP_ID_272444550 m1A Human chr6 - 33304397 33304396 33304398 GTCAGCCTCTCTGGGCACTTGCAGCCGCCCCCAGTCACCACTGAGCAGCATGGGGCACGCTATGC GTCAGCCTCTCTGGGCACTTGCAGCCGCCCC__GTCACCACTGAGCAGCATGGGGCACGCTATGC CTG C TAPBP Ensembl:ENSG00000231925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33304350..33304463 26863196 MeRIP-seq:(Medium) rs774468959 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_791536,Human_RBP_ID_22461222,Human_RBP_ID_22772725,Human_RBP_ID_27523979 75731 RMVar_ID_75731 Human_SNP_ID_272444566 m1A Human chr6 - 33304426 33304426 33304426 CGGCCCTGCGCCACCATTCCGATGGCTCTGTCAGCCTCTCTGGGCACTTGCAGCCGCCCCCAGTC CGGCCCTGCGCCACCATTCCGATGGCTCTGTCCGCCTCTCTGGGCACTTGCAGCCGCCCCCAGTC T G TAPBP Ensembl:ENSG00000231925 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33304319..33304667 32194978 MeRIP-seq:(Medium) rs1281620948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22772725 Human_miRNA_ID_1397403 75732 RMVar_ID_75732 Human_SNP_ID_272444653 m1A Human chr6 - 33304637 33304636 33304637 TCCCTATGCTCATTTCGTCCTCTTTCCCCAGAACCCCCCAAAGTGTCCCTGATGCCAGCAACCCT TCCCTATGCTCATTTCGTCCTCTTTCCCCAGA_CCCCCCAAAGTGTCCCTGATGCCAGCAACCCT GT G TAPBP Ensembl:ENSG00000231925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33304530..33304664 26863196 MeRIP-seq:(Medium) rs766321318 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_947560,Human_RBP_ID_22553708,Human_RBP_ID_22616228 Human_Splice_Rec_761544,Human_Splice_Rec_761560,Human_Splice_Rec_761572,Human_Splice_Rec_761586,Human_Splice_Rec_761604 75733 RMVar_ID_75733 Human_SNP_ID_272444753 m1A Human chr6 + 33304969 33304969 33304969 CACAATCCAGTGCCCACCCTCTACCCCTGGAGACCTCTGTCCCCCAACTCACTGTACACAGCAAG CACAATCCAGTGCCCACCCTCTACCCCTGGAGGCCTCTGTCCCCCAACTCACTGTACACAGCAAG A G RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33304968..33305072 26863196 MeRIP-seq:(Medium) rs1285998909 Functional Loss SNV dbSNP153 33..33 33 - - - 75734 RMVar_ID_75734 Human_SNP_ID_272444772 m1A Human chr6 - 33305040 33305037 33305040 AACCCTTTCAGGAGGGCACCTATCTGGCCACCATACACCTGCCATACCTGCAAGGACAGGTCACC AACCCTTTCAGGAGGGCACCTATCTGGCCACC___CACCTGCCATACCTGCAAGGACAGGTCACC GTAT G TAPBP Ensembl:ENSG00000231925 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33304976..33305375 32194978 MeRIP-seq:(Medium) rs753264936 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5152637,Human_RBP_ID_9336091,Human_RBP_ID_18085281,Human_RBP_ID_22461992,Human_RBP_ID_22772729,Human_RBP_ID_27523983 Human_Splice_Rec_761543,Human_Splice_Rec_761559,Human_Splice_Rec_761571,Human_Splice_Rec_761585,Human_Splice_Rec_761603 75735 RMVar_ID_75735 Human_SNP_ID_272444775 m1A Human chr6 - 33305040 33305040 33305040 AACCCTTTCAGGAGGGCACCTATCTGGCCACCATACACCTGCCATACCTGCAAGGACAGGTCACC AACCCTTTCAGGAGGGCACCTATCTGGCCACCTTACACCTGCCATACCTGCAAGGACAGGTCACC T A TAPBP Ensembl:ENSG00000231925 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33304976..33305375 32194978 MeRIP-seq:(Medium) rs771562168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5152637,Human_RBP_ID_9336091,Human_RBP_ID_18085281,Human_RBP_ID_22461992,Human_RBP_ID_22772729,Human_RBP_ID_27523983 Human_Splice_Rec_761543,Human_Splice_Rec_761559,Human_Splice_Rec_761571,Human_Splice_Rec_761585,Human_Splice_Rec_761603 75736 RMVar_ID_75736 Human_SNP_ID_272446889 m1A Human chr6 - 33313866 33313866 33313866 CAAACCGCTCCTCACTCGCGTCCCTATACGCCAGGCCTGGCGACCGCCGTCTCAGCAGGACCCGC CAAACCGCTCCTCACTCGCGTCCCTATACGCCGGGCCTGGCGACCGCCGTCTCAGCAGGACCCGC T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33313851..33313875 26863196 MeRIP-seq:(Medium) rs745433426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948666,Human_RBP_ID_4905447 75737 RMVar_ID_75737 Human_SNP_ID_272446999 m1A Human chr6 - 33314074 33314074 33314074 CTTTGGAGGAAAGTGAAAGTGAAAGGAGGAAGAGGAGGCTTCATGGCTGAGGAGGTCGCAGCGCC CTTTGGAGGAAAGTGAAAGTGAAAGGAGGAAGTGGAGGCTTCATGGCTGAGGAGGTCGCAGCGCC T A TAPBP Ensembl:ENSG00000231925 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33314026..33314250 26863196 MeRIP-seq:(Medium) rs1170609483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671758,Human_RBP_ID_18074431,Human_RBP_ID_18195790 Human_Splice_Rec_761537,Human_Splice_Rec_761551,Human_Splice_Rec_761567,Human_Splice_Rec_761579,Human_Splice_Rec_761591,Human_Splice_Rec_761597,Human_Splice_Rec_761605,Human_Splice_Rec_761609 75738 RMVar_ID_75738 Human_SNP_ID_272447000 m1A Human chr6 - 33314074 33314074 33314074 CTTTGGAGGAAAGTGAAAGTGAAAGGAGGAAGAGGAGGCTTCATGGCTGAGGAGGTCGCAGCGCC CTTTGGAGGAAAGTGAAAGTGAAAGGAGGAAGGGGAGGCTTCATGGCTGAGGAGGTCGCAGCGCC T C TAPBP Ensembl:ENSG00000231925 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33314026..33314250 26863196 MeRIP-seq:(Medium) rs1170609483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671758,Human_RBP_ID_18074431,Human_RBP_ID_18195790 Human_Splice_Rec_761537,Human_Splice_Rec_761551,Human_Splice_Rec_761567,Human_Splice_Rec_761579,Human_Splice_Rec_761591,Human_Splice_Rec_761597,Human_Splice_Rec_761605,Human_Splice_Rec_761609 75739 RMVar_ID_75739 Human_SNP_ID_272447234 m1A Human chr6 - 33314977 33314977 33314977 GGGCAGGCTACTGGGGTGGGGTAGCTTTCGGGAAAGGGAATAAGGAGCACGATGCAAGGGCGCTG GGGCAGGCTACTGGGGTGGGGTAGCTTTCGGGGAAGGGAATAAGGAGCACGATGCAAGGGCGCTG T C ZBTB22 Ensembl:ENSG00000236104 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33314907..33315187 26863196 MeRIP-seq:(Medium) rs1460296291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821162 75740 RMVar_ID_75740 Human_SNP_ID_272447246 m1A Human chr6 - 33315011 33315011 33315011 TGGGCTTCGGTGGAGGTGGAGGAGCAAACTGAAGGGGCAGGCTACTGGGGTGGGGTAGCTTTCGG TGGGCTTCGGTGGAGGTGGAGGAGCAAACTGAGGGGGCAGGCTACTGGGGTGGGGTAGCTTTCGG T C ZBTB22 Ensembl:ENSG00000236104 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33314981..33315305 26863196 MeRIP-seq:(Medium) rs1329765635 Functional Loss SNV dbSNP153 33..33 33 - - - 75741 RMVar_ID_75741 Human_SNP_ID_272447261 m1A Human chr6 - 33315062 33315062 33315062 CCCCGTCCAGCAGACGTGTCTGGTCCCCACCCAGAGTCCACAAGGTGGAGATGGGCTTCGGTGGA CCCCGTCCAGCAGACGTGTCTGGTCCCCACCCGGAGTCCACAAGGTGGAGATGGGCTTCGGTGGA T C ZBTB22 Ensembl:ENSG00000236104 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33315014..33315105 26863196 MeRIP-seq:(Medium) rs754370089 Functional Loss SNV dbSNP153 33..33 33 - - - 75742 RMVar_ID_75742 Human_SNP_ID_272447419 m1A Human chr6 + 33315457 33315457 33315457 TCTTGTGGGAGAAGGCCTTCCCACAATGGCACAGAAAGATCTTATTCCCGTCCCCACTGCCAGTC TCTTGTGGGAGAAGGCCTTCCCACAATGGCACTGAAAGATCTTATTCCCGTCCCCACTGCCAGTC A T RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33315407..33315715 26863196 MeRIP-seq:(Medium) rs1301390667 Functional Loss SNV dbSNP153 33..33 33 - - - 75743 RMVar_ID_75743 Human_SNP_ID_272447592 m1A Human chr6 - 33315867 33315867 33315867 CTAGGGGGTAGCTCCAGGGTTCCAGTGGGGGGAGGGCCTGAGGCTACCCTCAGCATAAGTGATGT CTAGGGGGTAGCTCCAGGGTTCCAGTGGGGGGGGGGCCTGAGGCTACCCTCAGCATAAGTGATGT T C ZBTB22 Ensembl:ENSG00000236104 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33315821..33316171 26863196 MeRIP-seq:(Medium) rs1554280356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_215196,Human_RBP_ID_4903271,Human_RBP_ID_22106789,Human_RBP_ID_22728150 75744 RMVar_ID_75744 Human_SNP_ID_272448691 m1A Human chr6 - 33319126 33319126 33319126 AGCCCACCTTCCCCCTTGGCTTCCTTGGCCCCAGTTGCTGATTCCTCCACGAGGGTGGACTCTCC AGCCCACCTTCCCCCTTGGCTTCCTTGGCCCCCGTTGCTGATTCCTCCACGAGGGTGGACTCTCC T G DAXX Ensembl:ENSG00000204209 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33319076..33319225 32194978 MeRIP-seq:(Medium) rs755659352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251847,Human_RBP_ID_662562,Human_RBP_ID_4884826,Human_RBP_ID_9400384,Human_RBP_ID_17664036,Human_RBP_ID_18085282,Human_RBP_ID_22831506,Human_RBP_ID_24158302,Human_RBP_ID_26535730 Human_Splice_Rec_761632,Human_Splice_Rec_761646,Human_Splice_Rec_761658,Human_Splice_Rec_761672 75745 RMVar_ID_75745 Human_SNP_ID_272448856 m1A Human chr6 - 33319626 33319626 33319626 GCTGACCCTGGAGGAAGAAAGCCCTGTGTCTCAGCTCTTTGAGCTAGAGATTGAAGCTTTGCCCC GCTGACCCTGGAGGAAGAAAGCCCTGTGTCTCCGCTCTTTGAGCTAGAGATTGAAGCTTTGCCCC T G DAXX Ensembl:ENSG00000204209 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33319576..33319825 32194978 MeRIP-seq:(Medium) rs910218439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8900566,Human_RBP_ID_9309680,Human_RBP_ID_9400387,Human_RBP_ID_26353800 75746 RMVar_ID_75746 Human_SNP_ID_272448916 m1A Human chr6 - 33319852 33319852 33319852 GCTACCCTCTCCCCTTTTCTTCTTTTCCAGGTAAAGATGGAGACAAGAGCCCCATGTCCTCACTA GCTACCCTCTCCCCTTTTCTTCTTTTCCAGGTGAAGATGGAGACAAGAGCCCCATGTCCTCACTA T C DAXX Ensembl:ENSG00000204209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33319676..33319875 26863196 MeRIP-seq:(Medium) rs1267106054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4884843,Human_RBP_ID_18863820,Human_RBP_ID_26353801,Human_RBP_ID_27827542 Human_Splice_Rec_761630,Human_Splice_Rec_761644,Human_Splice_Rec_761656,Human_Splice_Rec_761670,Human_Splice_Rec_761682,Human_Splice_Rec_761688,Human_Splice_Rec_761690 75747 RMVar_ID_75747 Human_SNP_ID_272448991 m1A Human chr6 - 33320064 33320064 33320064 TTCTGAAGAGGAGGAGGATCTGGAACAGATGCAGGAGGGTCAGGAGGATGATGAAGAGGAGGACG TTCTGAAGAGGAGGAGGATCTGGAACAGATGCTGGAGGGTCAGGAGGATGATGAAGAGGAGGACG T A DAXX Ensembl:ENSG00000204209 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33320001..33320150 26863196 MeRIP-seq:(Medium) rs1317065282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4884847,Human_RBP_ID_5152132,Human_RBP_ID_7594589,Human_RBP_ID_17663281,Human_RBP_ID_23067811,Human_RBP_ID_24158306,Human_RBP_ID_24548388,Human_RBP_ID_26353802,Human_RBP_ID_27827543 Human_Splice_Rec_761629,Human_Splice_Rec_761643,Human_Splice_Rec_761655,Human_Splice_Rec_761669,Human_Splice_Rec_761681,Human_Splice_Rec_761687,Human_Splice_Rec_761689 75748 RMVar_ID_75748 Human_SNP_ID_272449121 m1A Human chr6 - 33320409 33320409 33320409 GGCTCCAAGGCACCTCTTCCCACTCTGCAGACACCCCCGAAGCCTCCTTGGATTCTGGTGAGGTG GGCTCCAAGGCACCTCTTCCCACTCTGCAGACTCCCCCGAAGCCTCCTTGGATTCTGGTGAGGTG T A DAXX Ensembl:ENSG00000204209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33320385..33320539 26863196 MeRIP-seq:(Medium) rs1362269917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7594591,Human_RBP_ID_18863821,Human_RBP_ID_19130772,Human_RBP_ID_27524012 Human_Splice_Rec_761627,Human_Splice_Rec_761641,Human_Splice_Rec_761653,Human_Splice_Rec_761667,Human_Splice_Rec_761679,Human_Splice_Rec_761685 75749 RMVar_ID_75749 Human_SNP_ID_272449641 m1A Human chr6 - 33321910 33321910 33321910 GGGGGATTTGATCCCCTATGGCCACCGCTAACAGCATCATCGTGCTGGATGATGATGACGAAGAT GGGGGATTTGATCCCCTATGGCCACCGCTAACTGCATCATCGTGCTGGATGATGATGACGAAGAT T A SMIM40,DAXX Ensembl:ENSG00000285064,Ensembl:ENSG00000204209 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33321860..33321925 26863196 MeRIP-seq:(Medium) rs922397176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948177,Human_RBP_ID_4884911 Human_Splice_Rec_761622,Human_Splice_Rec_761636,Human_Splice_Rec_761662,Human_Splice_Rec_761694,Human_Splice_Rec_761698,Human_Splice_Rec_761700,Human_Splice_Rec_761704 75750 RMVar_ID_75750 Human_SNP_ID_272449942 m1A Human chr6 - 33322909 33322906 33322909 GGAGTGGGAAGGAAGGCGGAGGGAACCATGCGAGGTTCTGAGAATTGCGGCGAGGGTCGCCTCGA GGAGTGGGAAGGAAGGCGGAGGGAACCATGCG___TTCTGAGAATTGCGGCGAGGGTCGCCTCGA ACCT A SMIM40,DAXX Ensembl:ENSG00000285064,Ensembl:ENSG00000204209 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33322629..33322912 26863196 MeRIP-seq:(Medium) rs771493519 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1671806,Human_RBP_ID_4903932,Human_RBP_ID_22462000,Human_RBP_ID_24158315 Human_Splice_Rec_761621,Human_Splice_Rec_761635,Human_Splice_Rec_761649,Human_Splice_Rec_761661,Human_Splice_Rec_761677,Human_Splice_Rec_761691,Human_Splice_Rec_761693,Human_Splice_Rec_761697 75751 RMVar_ID_75751 Human_SNP_ID_272449943 m1A Human chr6 - 33322909 33322909 33322909 GGAGTGGGAAGGAAGGCGGAGGGAACCATGCGAGGTTCTGAGAATTGCGGCGAGGGTCGCCTCGA GGAGTGGGAAGGAAGGCGGAGGGAACCATGCGGGGTTCTGAGAATTGCGGCGAGGGTCGCCTCGA T C SMIM40,DAXX Ensembl:ENSG00000285064,Ensembl:ENSG00000204209 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33322629..33322912 26863196 MeRIP-seq:(Medium) rs1562734558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671806,Human_RBP_ID_4903932,Human_RBP_ID_22462000,Human_RBP_ID_24158315 Human_Splice_Rec_761621,Human_Splice_Rec_761635,Human_Splice_Rec_761649,Human_Splice_Rec_761661,Human_Splice_Rec_761677,Human_Splice_Rec_761691,Human_Splice_Rec_761693,Human_Splice_Rec_761697 75752 RMVar_ID_75752 Human_SNP_ID_272449945 m1A Human chr6 + 33322913 33322913 33322913 GGCGACCCTCGCCGCAATTCTCAGAACCTCGCATGGTTCCCTCCGCCTTCCTTCCCACTCCCACC GGCGACCCTCGCCGCAATTCTCAGAACCTCGCGTGGTTCCCTCCGCCTTCCTTCCCACTCCCACC A G RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33322609..33322950 26863196 MeRIP-seq:(Medium) rs1299535357 Functional Loss SNV dbSNP153 33..33 33 - - - 75753 RMVar_ID_75753 Human_SNP_ID_272468114 m1A Human chr6 + 33398334 33398334 33398334 CCTGGGTGCAACGACCAAAATTACCACATCCCACCCAAGAGTTCCATCCCTCACTACAGTGCCAC CCTGGGTGCAACGACCAAAATTACCACATCCCGCCCAAGAGTTCCATCCCTCACTACAGTGCCAC A G KIFC1 Ensembl:ENSG00000237649 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33398165..33398387 32194978 MeRIP-seq:(Medium) rs1329903242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1047132,Human_RBP_ID_5152134,Human_RBP_ID_5478114,Human_RBP_ID_8643055,Human_RBP_ID_17306769,Human_RBP_ID_17419809,Human_RBP_ID_17710624,Human_RBP_ID_18074457 Human_Splice_Rec_761714,Human_Splice_Rec_761715,Human_Splice_Rec_761734,Human_Splice_Rec_761735 RMVar_hsa_circ_107733,RMVar_hsa_circ_305629,RMVar_hsa_circ_237859 75754 RMVar_ID_75754 Human_SNP_ID_272468125 m1A Human chr6 + 33398384 33398384 33398384 TCACTACAGTGCCACAGACACAAGGCCAGACCACAGGTGGGCTCTCAGGATGGATAGACTCCAAG TCACTACAGTGCCACAGACACAAGGCCAGACCGCAGGTGGGCTCTCAGGATGGATAGACTCCAAG A G KIFC1 Ensembl:ENSG00000237649 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33398257..33398421 26863196 MeRIP-seq:(Medium) rs781332661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949407,Human_RBP_ID_9400395,Human_RBP_ID_15792322,Human_RBP_ID_19130775,Human_RBP_ID_24158326 Human_Splice_Rec_761714,Human_Splice_Rec_761715,Human_Splice_Rec_761734,Human_Splice_Rec_761735 RMVar_hsa_circ_107733,RMVar_hsa_circ_305629,RMVar_hsa_circ_237859 75755 RMVar_ID_75755 Human_SNP_ID_272469443 m1A Human chr6 + 33404086 33404020 33404086 GCAAGAGCTTCAGAAAAAACAGGTGGAATTGCAGGAAGAACGGAGGGGACTGATGTCCCAACTAG _________________________________GGAAGAACGGAGGGGACTGATGTCCCAACTAG TGGAAGAGCGGCTGAGCACGCAGGAGGGCTTGGTGCAAGAGCTTCAGAAAAAACAGGTGGAATTGCA T KIFC1 Ensembl:ENSG00000237649 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33403789..33404151 26863196 MeRIP-seq:(Medium) rs1562835250 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_790744,Human_RBP_ID_947567,Human_RBP_ID_1671821,Human_RBP_ID_3806972,Human_RBP_ID_3968957,Human_RBP_ID_4884974,Human_RBP_ID_7594638,Human_RBP_ID_9400399,Human_RBP_ID_22104983,Human_RBP_ID_26353805,Human_RBP_ID_27828487 Human_Splice_Rec_761721 RMVar_hsa_circ_107733,RMVar_hsa_circ_237859 75756 RMVar_ID_75756 Human_SNP_ID_272472522 m1A Human chr6 - 33414028 33414028 33414028 AGCATTCAAATTCATAGAACCTGGACATGGGCAAGAGGGAGCAAACACACTTACACAGGAAAACT AGCATTCAAATTCATAGAACCTGGACATGGGCGAGAGGGAGCAAACACACTTACACAGGAAAACT T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33414026..33414075 32194978 MeRIP-seq:(Medium) rs771789201 Functional Loss SNV dbSNP153 33..33 33 - - - 75757 RMVar_ID_75757 Human_SNP_ID_272472762 m1A Human chr6 + 33414825 33414825 33414825 CTGTGGAGCCCCCTACTGGAGATGGAGCACTCACCAGGTCACTGGTCCAGGGGGGATGGGGGAAA CTGTGGAGCCCCCTACTGGAGATGGAGCACTCTCCAGGTCACTGGTCCAGGGGGGATGGGGGAAA A T PHF1 Ensembl:ENSG00000112511 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33414776..33414825 32194978 MeRIP-seq:(Medium) rs763272948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23067348 Human_Splice_Rec_761783,Human_Splice_Rec_761829,Human_Splice_Rec_761855,Human_Splice_Rec_761883 75758 RMVar_ID_75758 Human_SNP_ID_272473445 m1A Human chr6 + 33416657 33416657 33416657 TCATGATGAGCAGGAACAGGGCTCATCATGGCAGGACTGTGATAGAGTCAGAAACTGACTCTGTG TCATGATGAGCAGGAACAGGGCTCATCATGGCCGGACTGTGATAGAGTCAGAAACTGACTCTGTG A C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33416606..33416689 26863196 MeRIP-seq:(Medium) rs1041056174 Functional Loss SNV dbSNP153 33..33 33 - - - 75759 RMVar_ID_75759 Human_SNP_ID_272473518 m1A Human chr6 + 33416775 33416775 33416775 AATTACCTCGGCCACTTCGTAAGGGTGCACAGAACTACAAAATAGGTGGGTGGGGGAAGGGGATC AATTACCTCGGCCACTTCGTAAGGGTGCACAGGACTACAAAATAGGTGGGTGGGGGAAGGGGATC A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33416601..33416837 32194978 MeRIP-seq:(Medium) rs775099271 Functional Loss SNV dbSNP153 33..33 33 - - - 75760 RMVar_ID_75760 Human_SNP_ID_272473707 m1A Human chr6 - 33417252 33417252 33417252 CCTGCGTCAACCTCATCCCTCAGATTACATCCATGTGAGTCATAGGAGTTGGGGGGTTAACCTAA CCTGCGTCAACCTCATCCCTCAGATTACATCCGTGTGAGTCATAGGAGTTGGGGGGTTAACCTAA T C CUTA Ensembl:ENSG00000112514 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33417076..33417330 32194978 MeRIP-seq:(Medium) rs1487512960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948676,Human_RBP_ID_1671846,Human_RBP_ID_18085283,Human_RBP_ID_19018376,Human_RBP_ID_19129127 Human_Splice_Rec_761912,Human_Splice_Rec_761913,Human_Splice_Rec_761922,Human_Splice_Rec_761923,Human_Splice_Rec_761930,Human_Splice_Rec_761936,Human_Splice_Rec_761937,Human_Splice_Rec_761946,Human_Splice_Rec_761947,Human_Splice_Rec_761956,Human_Splice_Rec_761957,Human_Splice_Rec_761966,Human_Splice_Rec_761967,Human_Splice_Rec_761978,Human_Splice_Rec_761979,Human_Splice_Rec_761986,Human_Splice_Rec_761987,Human_Splice_Rec_761996,Human_Splice_Rec_761997,Human_Splice_Rec_762003,Human_Splice_Rec_762010,Human_Splice_Rec_762011,Human_Splice_Rec_762018,Human_Splice_Rec_762022,Human_Splice_Rec_762023 Human_miRNA_ID_2191451,Human_miRNA_ID_2191452 RMVar_hsa_circ_95957,RMVar_hsa_circ_112562,RMVar_hsa_circ_237863,RMVar_hsa_circ_237864 75761 RMVar_ID_75761 Human_SNP_ID_272473841 m1A Human chr6 + 33417602 33417602 33417602 GGCCGGCGAGGGCTGGGTCGGAGGGCTTCCAGAGGCCATGGTCAGCAAGACTCGGGGTAGCAACA GGCCGGCGAGGGCTGGGTCGGAGGGCTTCCAGGGGCCATGGTCAGCAAGACTCGGGGTAGCAACA A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33417551..33418175 26863196 MeRIP-seq:(Medium) rs1053037060 Functional Loss SNV dbSNP153 33..33 33 - - - 75762 RMVar_ID_75762 Human_SNP_ID_272473876 m1A Human chr6 + 33417685 33417685 33417685 GCAGCAGCGCCGGCATCCAAACAAAAGACAGGAGCAGAGAGGCCTGAGAGCAGGAGGCGAATTCG GCAGCAGCGCCGGCATCCAAACAAAAGACAGGGGCAGAGAGGCCTGAGAGCAGGAGGCGAATTCG A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33417468..33418200 26863196 MeRIP-seq:(Medium) rs763567192 Functional Loss SNV dbSNP153 33..33 33 - - - 75763 RMVar_ID_75763 Human_SNP_ID_272473880 m1A Human chr6 + 33417692 33417692 33417692 CGCCGGCATCCAAACAAAAGACAGGAGCAGAGAGGCCTGAGAGCAGGAGGCGAATTCGATCTCTC CGCCGGCATCCAAACAAAAGACAGGAGCAGAGGGGCCTGAGAGCAGGAGGCGAATTCGATCTCTC A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33417476..33417900 32194978 MeRIP-seq:(Medium) rs1007878051 Functional Loss SNV dbSNP153 33..33 33 - - - 75764 RMVar_ID_75764 Human_SNP_ID_272473978 m1A Human chr6 + 33417953 33417950 33417954 CGAGGACCGGAAGGGGCGGGGCGGGGCCGGTCACTCACCACTCCGCCGAGCAGGACCGCGGGAGC CGAGGACCGGAAGGGGCGGGGCGGGGCCGG____TCACCACTCCGCCGAGCAGGACCGCGGGAGC GTCAC G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33417951..33418050 32194978 MeRIP-seq:(Medium) rs759656326 Functional Loss DEL dbSNP153 31..34 33 - - - 75765 RMVar_ID_75765 Human_SNP_ID_272474608 m1A Human chr6 + 33420298 33420296 33420298 TGAGCAGGTCTCGAGCCTCCATCCATCGGGGGAGCATCCCCGCGATGTCCTATGCCCCCTTCAGA TGAGCAGGTCTCGAGCCTCCATCCATCGGGG__GCATCCCCGCGATGTCCTATGCCCCCTTCAGA GGA G SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33420106..33420748 32194978 MeRIP-seq:(Medium) rs1554304254 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_762034,Human_Splice_Rec_762035,Human_Splice_Rec_762059,Human_Splice_Rec_762095,Human_Splice_Rec_762113,Human_Splice_Rec_762149,Human_Splice_Rec_762183,Human_Splice_Rec_762215,Human_Splice_Rec_762251,Human_Splice_Rec_762285 Clinvar_Rec_347 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75766 RMVar_ID_75766 Human_SNP_ID_272475810 m1A Human chr6 + 33425846 33425846 33425846 TCCGGGACCGGAGGAGCGAGTCCAGTCGCAACAAACTGCTGAGACGCACAGTCTCCGTGCCGGTG TCCGGGACCGGAGGAGCGAGTCCAGTCGCAACTAACTGCTGAGACGCACAGTCTCCGTGCCGGTG A T SYNGAP1 Ensembl:ENSG00000197283 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33425827..33425953 26863196 MeRIP-seq:(Medium) rs1554119823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_762038,Human_Splice_Rec_762039,Human_Splice_Rec_762062,Human_Splice_Rec_762063,Human_Splice_Rec_762098,Human_Splice_Rec_762099,Human_Splice_Rec_762116,Human_Splice_Rec_762117,Human_Splice_Rec_762152,Human_Splice_Rec_762153,Human_Splice_Rec_762186,Human_Splice_Rec_762187,Human_Splice_Rec_762218,Human_Splice_Rec_762219,Human_Splice_Rec_762254,Human_Splice_Rec_762255,Human_Splice_Rec_762288,Human_Splice_Rec_762289,Human_Splice_Rec_762330,Human_Splice_Rec_762332,Human_Splice_Rec_762334,Human_Splice_Rec_762336,Human_Splice_Rec_762338 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75767 RMVar_ID_75767 Human_SNP_ID_272476390 m1A Human chr6 + 33428222 33428222 33428222 GGGCGGGGGCGCGCGTGTGCGTGGGCGCGGGGAGGGGGGTGGGGAAGCCGCGGTGGCGGCGGCGG GGGCGGGGGCGCGCGTGTGCGTGGGCGCGGGGGGGGGGGTGGGGAAGCCGCGGTGGCGGCGGCGG A G SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33428214..33428386 26863196 MeRIP-seq:(Medium) rs1051586225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13421,Human_RBP_ID_9336622,Human_RBP_ID_27842442 Human_Splice_Rec_762345 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75768 RMVar_ID_75768 Human_SNP_ID_272476391 m1A Human chr6 + 33428222 33428222 33428222 GGGCGGGGGCGCGCGTGTGCGTGGGCGCGGGGAGGGGGGTGGGGAAGCCGCGGTGGCGGCGGCGG GGGCGGGGGCGCGCGTGTGCGTGGGCGCGGGGTGGGGGGTGGGGAAGCCGCGGTGGCGGCGGCGG A T SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33428214..33428386 26863196 MeRIP-seq:(Medium) rs1051586225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13421,Human_RBP_ID_9336622,Human_RBP_ID_27842442 Human_Splice_Rec_762345 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75769 RMVar_ID_75769 Human_SNP_ID_272476533 m1A Human chr6 - 33428768 33428767 33428768 ACTCAGGCCAGTGCTGGAACACACATGCAAAGACACACACCTGCCACCAGGGACACAGAAAATCC ACTCAGGCCAGTGCTGGAACACACATGCAAAG_CACACACCTGCCACCAGGGACACAGAAAATCC GT G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33428766..33428853 26863196 MeRIP-seq:(Medium) rs1470935405 Functional Loss DEL dbSNP153 33..33 33 - - - 75770 RMVar_ID_75770 Human_SNP_ID_272476534 m1A Human chr6 - 33428768 33428768 33428768 ACTCAGGCCAGTGCTGGAACACACATGCAAAGACACACACCTGCCACCAGGGACACAGAAAATCC ACTCAGGCCAGTGCTGGAACACACATGCAAAGCCACACACCTGCCACCAGGGACACAGAAAATCC T G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33428766..33428853 26863196 MeRIP-seq:(Medium) rs1429345323 Functional Loss SNV dbSNP153 33..33 33 - - - 75771 RMVar_ID_75771 Human_SNP_ID_272476581 m1A Human chr6 + 33428971 33428971 33428971 GCTTGGTCAGTAAGTGGGGACAGAAAAGCTTAAAAAGGGAAGAAATGGGGTAAAGAGGAAAAGTG GCTTGGTCAGTAAGTGGGGACAGAAAAGCTTATAAAGGGAAGAAATGGGGTAAAGAGGAAAAGTG A T SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33428964..33429289 26863196 MeRIP-seq:(Medium) rs1278820345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75772 RMVar_ID_75772 Human_SNP_ID_272476587 m1A Human chr6 + 33428997 33428997 33428997 AGCTTAAAAAGGGAAGAAATGGGGTAAAGAGGAAAAGTGGGGAGGGGATAGGAGAGAAGGAATGA AGCTTAAAAAGGGAAGAAATGGGGTAAAGAGGGAAAGTGGGGAGGGGATAGGAGAGAAGGAATGA A G SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33428993..33429258 26863196 MeRIP-seq:(Medium) rs937110984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24158469 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648 75773 RMVar_ID_75773 Human_SNP_ID_272478667 m1A Human chr6 + 33437753 33437753 33437753 GGAGCTGCCCCCCAAGAAGCGGTACTACTGTGAGCTCTGCCTGGATGACATGCTGTATGCACGCA GGAGCTGCCCCCCAAGAAGCGGTACTACTGTGCGCTCTGCCTGGATGACATGCTGTATGCACGCA A C SYNGAP1 Ensembl:ENSG00000197283 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33437704..33437954 32194978 MeRIP-seq:(Medium) rs1471672432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24158523 Human_Splice_Rec_762048,Human_Splice_Rec_762072,Human_Splice_Rec_762108,Human_Splice_Rec_762126,Human_Splice_Rec_762162,Human_Splice_Rec_762196,Human_Splice_Rec_762228,Human_Splice_Rec_762264,Human_Splice_Rec_762298,Human_Splice_Rec_762356,Human_Splice_Rec_762388 Human_miRNA_ID_2285097,Human_miRNA_ID_2288096 RMVar_hsa_circ_237865,RMVar_hsa_circ_90648,RMVar_hsa_circ_35214,RMVar_hsa_circ_268503 75774 RMVar_ID_75774 Human_SNP_ID_272481245 m1A Human chr6 + 33446656 33446656 33446656 TGTCCAACCGGAAGCTGGAAGAGTATGAGCGGAGGCTGCTGTCCCAGGAAGAACAAACCAGCAAA TGTCCAACCGGAAGCTGGAAGAGTATGAGCGGCGGCTGCTGTCCCAGGAAGAACAAACCAGCAAA A C SYNGAP1 Ensembl:ENSG00000197283 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33446546..33446783 26863196 MeRIP-seq:(Medium) rs1329089523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968974,Human_RBP_ID_19018384,Human_RBP_ID_26353824,Human_RBP_ID_27827558 Human_Splice_Rec_762090,Human_Splice_Rec_762144,Human_Splice_Rec_762180,Human_Splice_Rec_762212,Human_Splice_Rec_762246,Human_Splice_Rec_762282,Human_Splice_Rec_762316,Human_Splice_Rec_762374,Human_Splice_Rec_762406 RMVar_hsa_circ_269040 75775 RMVar_ID_75775 Human_SNP_ID_272481277 m1A Human chr6 - 33446780 33446780 33446780 AACCCCCTCCCCAGGCCGCCCCTCACCTGCCAATGATGCTCTTGATCTGGGAATCCTTCTCTGCC AACCCCCTCCCCAGGCCGCCCCTCACCTGCCAGTGATGCTCTTGATCTGGGAATCCTTCTCTGCC T C SYNGAP1-AS1 Ensembl:ENSG00000274259 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33446729..33454015 32194978 MeRIP-seq:(Medium) rs1451330589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_762422 75776 RMVar_ID_75776 Human_SNP_ID_272481739 m1A Human chr6 + 33448996 33448996 33448996 TCCGACACCTGCACAGATCCATCTCCCAAGACACCACCCAAAGAGAGCATTTGCTGCTGCTTCCC TCCGACACCTGCACAGATCCATCTCCCAAGACGCCACCCAAAGAGAGCATTTGCTGCTGCTTCCC A G SYNGAP1 Ensembl:ENSG00000197283 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33448947..33449068 26863196 MeRIP-seq:(Medium) rs751146111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3003938 RMVar_hsa_circ_269040 75777 RMVar_ID_75777 Human_SNP_ID_272482641 m1A Human chr6 - 33453151 33453151 33453151 GAGTCTAGGAGAGTCTCAATACCAAACGCAAAAGGATGAAGGGGGCAAGGCTGGGTAGGGGACAG GAGTCTAGGAGAGTCTCAATACCAAACGCAAATGGATGAAGGGGGCAAGGCTGGGTAGGGGACAG T A SYNGAP1-AS1 Ensembl:ENSG00000274259 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33453148..33453295 26863196 MeRIP-seq:(Medium) rs915393014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3820777,Human_RBP_ID_5622093 75778 RMVar_ID_75778 Human_SNP_ID_272483040 m1A Human chr6 + 33454624 33454624 33454624 CGGAGCTGTAGCGGCACTGTAACTGCGAGGGCAGCGCCGCGTGTGTAACGGCGGGGGCGTGTCGG CGGAGCTGTAGCGGCACTGTAACTGCGAGGGCGGCGCCGCGTGTGTAACGGCGGGGGCGTGTCGG A G ZBTB9 Ensembl:ENSG00000213588 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:33454601..33454752 26863196 MeRIP-seq:(Medium) rs1238296053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903945 Human_Splice_Rec_762427 RMVar_hsa_circ_86328,RMVar_hsa_circ_237867 75779 RMVar_ID_75779 Human_SNP_ID_272499243 m1A Human chr6 - 33520987 33520987 33520987 GGGGGGGGGGGGGGGTGGTGGTGGTGTCGGATAAGGGAATAAAAGCAGGCTGCAATCTGCTCAGG GGGGGGGGGGGGGGGTGGTGGTGGTGTCGGATGAGGGAATAAAAGCAGGCTGCAATCTGCTCAGG T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:33520976..33521050 26863196 MeRIP-seq:(Medium) rs1561815846 Functional Loss SNV dbSNP153 33..33 33 - - - 75780 RMVar_ID_75780 Human_SNP_ID_272514677 m1A Human chr6 - 33578683 33578683 33578683 ATGAGGGGTCACAGCAGGTTGGGGCTGCGGTCAGGACCAGGCAAAGAGGAAAATTGGGGCCGGGG ATGAGGGGTCACAGCAGGTTGGGGCTGCGGTCGGGACCAGGCAAAGAGGAAAATTGGGGCCGGGG T C BAK1 Ensembl:ENSG00000030110 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33578662..33578775 26863196 MeRIP-seq:(Medium) rs1354593504 Functional Loss SNV dbSNP153 33..33 33 - - - 75781 RMVar_ID_75781 Human_SNP_ID_272525242 m1A Human chr6 + 33621479 33621479 33621479 CCCGTGGCCGCCAGCCCGCCCCGGCCGCACCGAGCGTCGGGATCCGAGGTGGGAGCGTACCCCTC CCCGTGGCCGCCAGCCCGCCCCGGCCGCACCGGGCGTCGGGATCCGAGGTGGGAGCGTACCCCTC A G ITPR3 Ensembl:ENSG00000096433 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:33621432..33621558 26863196 MeRIP-seq:(Medium) rs1174423449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903280,Human_RBP_ID_22534196 RMVar_hsa_circ_100275,RMVar_hsa_circ_237872 75782 RMVar_ID_75782 Human_SNP_ID_272525270 m1A Human chr6 + 33621575 33621575 33621575 TGAGCTTGGCCACGCGCCCCTAGGCGCCCCCCACGCCCTGGGCCCCGGAGGGCCGCAGCCATGAG TGAGCTTGGCCACGCGCCCCTAGGCGCCCCCCGCGCCCTGGGCCCCGGAGGGCCGCAGCCATGAG A G ITPR3 Ensembl:ENSG00000096433 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33621407..33621600 26863196 MeRIP-seq:(Medium) rs1349039642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4912785 RMVar_hsa_circ_100275,RMVar_hsa_circ_237872 75783 RMVar_ID_75783 Human_SNP_ID_272526801 m1A Human chr6 - 33628588 33628588 33628588 CCAGTTCCATCCCCAGCCCACACCCTGGACTCACTGTGTTGTGAACGCCCAGCCTCATTTCTGCA CCAGTTCCATCCCCAGCCCACACCCTGGACTCGCTGTGTTGTGAACGCCCAGCCTCATTTCTGCA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:33628585..33628714 26863196 MeRIP-seq:(Medium) rs1485663130 Functional Loss SNV dbSNP153 33..33 33 - - - 75784 RMVar_ID_75784 Human_SNP_ID_272526803 m1A Human chr6 + 33628595 33628595 33628595 ATGAGGCTGGGCGTTCACAACACAGTGAGTCCAGGGTGTGGGCTGGGGATGGAACTGGGTGGAGC ATGAGGCTGGGCGTTCACAACACAGTGAGTCCTGGGTGTGGGCTGGGGATGGAACTGGGTGGAGC A T ITPR3 Ensembl:ENSG00000096433 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33628589..33628672 26863196 MeRIP-seq:(Medium) rs947086994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100275,RMVar_hsa_circ_237872 75785 RMVar_ID_75785 Human_SNP_ID_272527864 m1A Human chr6 + 33633464 33633464 33633464 TTTGATAAACACAGGTGCCCGCCATGAGGAAGAGTCGGGGTGGGGCGCTAAGGCCAGGGACGTCG TTTGATAAACACAGGTGCCCGCCATGAGGAAGCGTCGGGGTGGGGCGCTAAGGCCAGGGACGTCG A C ITPR3 Ensembl:ENSG00000096433 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:33633460..33633693;chr6:33633447..33633715 26863196 MeRIP-seq:(Medium) rs1256238810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100275,RMVar_hsa_circ_237872 75786 RMVar_ID_75786 Human_SNP_ID_272529960 m1A Human chr6 + 33642334 33642334 33642334 CCTCTCCTGGAGTCAGAAATGGGAGGGCGTTGAGGCTGCAGATGGAGGCTAGATTGCCATCTAGT CCTCTCCTGGAGTCAGAAATGGGAGGGCGTTGCGGCTGCAGATGGAGGCTAGATTGCCATCTAGT A C ITPR3 Ensembl:ENSG00000096433 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:33642333..33642580 26863196 MeRIP-seq:(Medium) rs1167917836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_237873 75787 RMVar_ID_75787 Human_SNP_ID_272532874 m1A Human chr6 + 33655877 33655877 33655877 CAAGGAGAAGATCGCTGATGTGGTGTTGCTGCAGAAGCTGCAGGTATGTGTGTGTGTGCAGGCGT CAAGGAGAAGATCGCTGATGTGGTGTTGCTGCGGAAGCTGCAGGTATGTGTGTGTGTGCAGGCGT A G ITPR3 Ensembl:ENSG00000096433 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33655826..33655913 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_19018389,Human_RBP_ID_19130797,Human_RBP_ID_26353826 Human_Splice_Rec_762513,Human_Splice_Rec_762627 Human_miRNA_ID_2012106,Human_miRNA_ID_2758472 RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_269756,RMVar_hsa_circ_237873,RMVar_hsa_circ_324486 75788 RMVar_ID_75788 Human_SNP_ID_272533939 m1A Human chr6 - 33660188 33660188 33660188 TCAAGACCGTCTACACCCCGTCTGCTGGTTCCATCCCTTGCAGCCCCACCCAAGAGACATCTGAA TCAAGACCGTCTACACCCCGTCTGCTGGTTCCGTCCCTTGCAGCCCCACCCAAGAGACATCTGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:33660020..33660320;chr6:33660046..33660318 26863196 MeRIP-seq:(Medium) rs940509432 Functional Loss SNV dbSNP153 33..33 33 - - - 75789 RMVar_ID_75789 Human_SNP_ID_272536648 m1A Human chr6 + 33670450 33670450 33670450 CCTGTGCATGGCAGACGAGATGCTGCCCTTTGACCTGCGCGCCTCCTTCTGCCACCTGATGCTGC CCTGTGCATGGCAGACGAGATGCTGCCCTTTGGCCTGCGCGCCTCCTTCTGCCACCTGATGCTGC A G ITPR3 Ensembl:ENSG00000096433 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33670401..33670500 32194978 MeRIP-seq:(Medium) rs1001895508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79183,Human_RBP_ID_18195542 RMVar_hsa_circ_121196,RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_120357,RMVar_hsa_circ_90473,RMVar_hsa_circ_237873,RMVar_hsa_circ_103819,RMVar_hsa_circ_237874,RMVar_hsa_circ_237875,RMVar_hsa_circ_237876,RMVar_hsa_circ_127274,RMVar_hsa_circ_237878,RMVar_hsa_circ_126349,RMVar_hsa_circ_84728,RMVar_hsa_circ_116868,RMVar_hsa_circ_115659,RMVar_hsa_circ_104279,RMVar_hsa_circ_237882,RMVar_hsa_circ_237883,RMVar_hsa_circ_237880,RMVar_hsa_circ_237881,RMVar_hsa_circ_237879,RMVar_hsa_circ_119473,RMVar_hsa_circ_124935,RMVar_hsa_circ_237886,RMVar_hsa_circ_237887,RMVar_hsa_circ_237889,RMVar_hsa_circ_106042,RMVar_hsa_circ_237888,RMVar_hsa_circ_127782,RMVar_hsa_circ_107920,RMVar_hsa_circ_80690,RMVar_hsa_circ_86918,RMVar_hsa_circ_117273,RMVar_hsa_circ_237891,RMVar_hsa_circ_122335,RMVar_hsa_circ_237892,RMVar_hsa_circ_237893,RMVar_hsa_circ_87977,RMVar_hsa_circ_100169,RMVar_hsa_circ_237894,RMVar_hsa_circ_237895,RMVar_hsa_circ_80782,RMVar_hsa_circ_117480,RMVar_hsa_circ_237897,RMVar_hsa_circ_237899,RMVar_hsa_circ_76223,RMVar_hsa_circ_237898,RMVar_hsa_circ_237896,RMVar_hsa_circ_112834,RMVar_hsa_circ_127743,RMVar_hsa_circ_237900,RMVar_hsa_circ_122562,RMVar_hsa_circ_108529,RMVar_hsa_circ_237904,RMVar_hsa_circ_93437,RMVar_hsa_circ_102430,RMVar_hsa_circ_237906,RMVar_hsa_circ_237908,RMVar_hsa_circ_85132,RMVar_hsa_circ_237907,RMVar_hsa_circ_237905,RMVar_hsa_circ_237902,RMVar_hsa_circ_237903,RMVar_hsa_circ_237901 75790 RMVar_ID_75790 Human_SNP_ID_272537178 m1A Human chr6 - 33672100 33672100 33672100 CCCAGCAGACAGGCTGGGGGCACTGAAGACGGACTGCTTGCGGCTCAGCACCATGGTGGACATCA CCCAGCAGACAGGCTGGGGGCACTGAAGACGGGCTGCTTGCGGCTCAGCACCATGGTGGACATCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33672051..33672200 32194978 MeRIP-seq:(Medium) rs1435932617 Functional Loss SNV dbSNP153 33..33 33 - - - 75791 RMVar_ID_75791 Human_SNP_ID_272537179 m1A Human chr6 - 33672100 33672100 33672100 CCCAGCAGACAGGCTGGGGGCACTGAAGACGGACTGCTTGCGGCTCAGCACCATGGTGGACATCA CCCAGCAGACAGGCTGGGGGCACTGAAGACGGCCTGCTTGCGGCTCAGCACCATGGTGGACATCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33672051..33672200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 75792 RMVar_ID_75792 Human_SNP_ID_272540034 m1A Human chr6 + 33682576 33682576 33682576 GCAGCTGCTGCAGTCTACCACACGCCTCCTCGAGTGTCCGTGGCTACAGCAGCAGCACAAGGGCT GCAGCTGCTGCAGTCTACCACACGCCTCCTCGCGTGTCCGTGGCTACAGCAGCAGCACAAGGGCT A C ITPR3 Ensembl:ENSG00000096433 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33682526..33682625 32194978 MeRIP-seq:(Medium) rs572195243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79213 Human_Splice_Rec_762574,Human_Splice_Rec_762575,Human_Splice_Rec_762688,Human_Splice_Rec_762689 Human_miRNA_ID_2088703,Human_miRNA_ID_2089582 RMVar_hsa_circ_121196,RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_237873,RMVar_hsa_circ_103819,RMVar_hsa_circ_237875,RMVar_hsa_circ_126349,RMVar_hsa_circ_116868,RMVar_hsa_circ_104279,RMVar_hsa_circ_237880,RMVar_hsa_circ_237881,RMVar_hsa_circ_237879,RMVar_hsa_circ_119473,RMVar_hsa_circ_124935,RMVar_hsa_circ_237886,RMVar_hsa_circ_237889,RMVar_hsa_circ_237888,RMVar_hsa_circ_107920,RMVar_hsa_circ_80690,RMVar_hsa_circ_86918,RMVar_hsa_circ_117273,RMVar_hsa_circ_237892,RMVar_hsa_circ_100169,RMVar_hsa_circ_237895,RMVar_hsa_circ_117480,RMVar_hsa_circ_237897,RMVar_hsa_circ_237899,RMVar_hsa_circ_76223,RMVar_hsa_circ_237898,RMVar_hsa_circ_112834,RMVar_hsa_circ_237900,RMVar_hsa_circ_122562,RMVar_hsa_circ_237904,RMVar_hsa_circ_93437,RMVar_hsa_circ_237902,RMVar_hsa_circ_237903,RMVar_hsa_circ_237901,RMVar_hsa_circ_102196,RMVar_hsa_circ_113711,RMVar_hsa_circ_123707,RMVar_hsa_circ_237912,RMVar_hsa_circ_237913,RMVar_hsa_circ_237914,RMVar_hsa_circ_95901,RMVar_hsa_circ_237915,RMVar_hsa_circ_93001,RMVar_hsa_circ_113192,RMVar_hsa_circ_237916,RMVar_hsa_circ_77443,RMVar_hsa_circ_237917,RMVar_hsa_circ_237918 75793 RMVar_ID_75793 Human_SNP_ID_272542288 m1A Human chr6 - 33689289 33689286 33689289 TGTAGCGCTTGGTGAACAGGGCCGCGATGGAGAAGCAGATGAGGATCCAGAAGAGCAATGAGATG TGTAGCGCTTGGTGAACAGGGCCGCGATGGAG___CAGATGAGGATCCAGAAGAGCAATGAGATG GCTT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:33689226..33689325 26863196 MeRIP-seq:(Medium) rs776411484 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_15792899 75794 RMVar_ID_75794 Human_SNP_ID_272545580 m1A Human chr6 + 33701418 33701418 33701418 TCGTACATCTGATCACAGGCCTCAGGCTCTGCAACCTGAAAAGCAAAGAATCCCAAAGGAGGTGA TCGTACATCTGATCACAGGCCTCAGGCTCTGCCACCTGAAAAGCAAAGAATCCCAAAGGAGGTGA A C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:33701326..33701425;chr6:33701351..33701425 32194978 MeRIP-seq:(Medium) rs200778553 Functional Loss SNV dbSNP153 33..33 33 - - - 75795 RMVar_ID_75795 Human_SNP_ID_272548013 m1A Human chr6 + 33711528 33711528 33711528 GCCCCTGCCTCGTCCTTTCCTCCCCTCGTCCCAGCCGCCTCCCCGCCGGTCACCTGGGTATTCTC GCCCCTGCCTCGTCCTTTCCTCCCCTCGTCCCCGCCGCCTCCCCGCCGGTCACCTGGGTATTCTC A C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:33711526..33711575;chr6:33711526..33711700 26863196,32194978,32194978 MeRIP-seq:(Medium) rs773452279 Functional Loss SNV dbSNP153 33..33 33 - - - 75796 RMVar_ID_75796 Human_SNP_ID_272548064 m1A Human chr6 + 33711661 33711661 33711661 CGTCCACTGGCCATTCCTCACAGAGCTTAAGAAAACGCCGGTACCGGCTGGCCGCCATCTTGGGC CGTCCACTGGCCATTCCTCACAGAGCTTAAGACAACGCCGGTACCGGCTGGCCGCCATCTTGGGC A C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:33711494..33711725;chr6:33711497..33711725 26863196 MeRIP-seq:(Medium) rs969481609 Functional Loss SNV dbSNP153 33..33 33 - - - 75797 RMVar_ID_75797 Human_SNP_ID_272562312 m1A Human chr6 - 33772249 33772249 33772249 CGCCAGGGAGTCTGTCACCTGGGAGGTGGGGCAGGGATGGTGTTTCGGGTGGCGGGATGGGGAGC CGCCAGGGAGTCTGTCACCTGGGAGGTGGGGCGGGGATGGTGTTTCGGGTGGCGGGATGGGGAGC T C LEMD2 Ensembl:ENSG00000161904 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:33772199..33772394;chr6:33772201..33772356 26863196 MeRIP-seq:(Medium) rs1257535024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792253,Human_RBP_ID_5122231,Human_RBP_ID_5532408,Human_RBP_ID_8215995,Human_RBP_ID_9354644,Human_RBP_ID_9437418,Human_RBP_ID_18957317,Human_RBP_ID_26535782,Human_RBP_ID_26793017 Human_miRNA_ID_445527,Human_miRNA_ID_929309 75798 RMVar_ID_75798 Human_SNP_ID_272563556 m1A Human chr6 - 33777004 33777004 33777004 GTGGACTGGGAGCAGGACATGGAGCGCTATCCATATGTAGGCATCCTGCACGTGCGCGACAGCTT GTGGACTGGGAGCAGGACATGGAGCGCTATCCGTATGTAGGCATCCTGCACGTGCGCGACAGCTT T C LEMD2 Ensembl:ENSG00000161904 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33776932..33777033 32194978 MeRIP-seq:(Medium) rs757659513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947592,Human_RBP_ID_8900724,Human_RBP_ID_9401998,Human_RBP_ID_18370443,Human_RBP_ID_26355068,Human_RBP_ID_26535785 Human_Splice_Rec_762784,Human_Splice_Rec_762785,Human_Splice_Rec_762800,Human_Splice_Rec_762801,Human_Splice_Rec_762808,Human_Splice_Rec_762809,Human_Splice_Rec_762824,Human_Splice_Rec_762825,Human_Splice_Rec_762840,Human_Splice_Rec_762841,Human_Splice_Rec_762854,Human_Splice_Rec_762855,Human_Splice_Rec_762862,Human_Splice_Rec_762863,Human_Splice_Rec_762868,Human_Splice_Rec_762878,Human_Splice_Rec_762886 RMVar_hsa_circ_237932,RMVar_hsa_circ_123077,RMVar_hsa_circ_274548,RMVar_hsa_circ_330379,RMVar_hsa_circ_371471,RMVar_hsa_circ_128077,RMVar_hsa_circ_237934,RMVar_hsa_circ_119949,RMVar_hsa_circ_237933,RMVar_hsa_circ_237931 75799 RMVar_ID_75799 Human_SNP_ID_272564870 m1A Human chr6 - 33782119 33782117 33782119 AAAAGGAGGATGCTAGAAGCCACCTGTGTCTCAGGGGACCCCTGGGGTCAAGATCAACTTTGAAG AAAAGGAGGATGCTAGAAGCCACCTGTGTCTC__GGGACCCCTGGGGTCAAGATCAACTTTGAAG CCT C LEMD2 Ensembl:ENSG00000161904 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33782116..33782308 26863196 MeRIP-seq:(Medium) rs1411714646 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5216558 RMVar_hsa_circ_43913,RMVar_hsa_circ_274548,RMVar_hsa_circ_330379,RMVar_hsa_circ_128077,RMVar_hsa_circ_237931,RMVar_hsa_circ_374043,RMVar_hsa_circ_339535,RMVar_hsa_circ_237937 75800 RMVar_ID_75800 Human_SNP_ID_272564871 m1A Human chr6 - 33782119 33782119 33782119 AAAAGGAGGATGCTAGAAGCCACCTGTGTCTCAGGGGACCCCTGGGGTCAAGATCAACTTTGAAG AAAAGGAGGATGCTAGAAGCCACCTGTGTCTCCGGGGACCCCTGGGGTCAAGATCAACTTTGAAG T G LEMD2 Ensembl:ENSG00000161904 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:33782116..33782308 26863196 MeRIP-seq:(Medium) rs1397319553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5216558 RMVar_hsa_circ_43913,RMVar_hsa_circ_274548,RMVar_hsa_circ_330379,RMVar_hsa_circ_128077,RMVar_hsa_circ_237931,RMVar_hsa_circ_374043,RMVar_hsa_circ_339535,RMVar_hsa_circ_237937 75801 RMVar_ID_75801 Human_SNP_ID_272566395 m1A Human chr6 - 33788528 33788528 33788528 GGGCGACTCGAGCGGGCCCTGCTGGCGCGGCGAGGGCCCGGCCTGAGGTGGGGCGCCGGCTGGAG GGGCGACTCGAGCGGGCCCTGCTGGCGCGGCGGGGGCCCGGCCTGAGGTGGGGCGCCGGCTGGAG T C LEMD2 Ensembl:ENSG00000161904 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33788486..33789036 32194978 MeRIP-seq:(Medium) rs1343822151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17164358,Human_RBP_ID_22461241 RMVar_hsa_circ_128077,RMVar_hsa_circ_237931 75802 RMVar_ID_75802 Human_SNP_ID_272566590 m1A Human chr6 - 33788974 33788974 33788974 CCTGCGGGGCGAGGCCCGGCTGCGCGACGAGGAGCGGCTGCGGGAGGAGGCCCGGCCGCGGGGCG CCTGCGGGGCGAGGCCCGGCTGCGCGACGAGGCGCGGCTGCGGGAGGAGGCCCGGCCGCGGGGCG T G LEMD2 Ensembl:ENSG00000161904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33788923..33789118 26863196 MeRIP-seq:(Medium) rs776365970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842078,Human_RBP_ID_4903286,Human_RBP_ID_18074594,Human_RBP_ID_22461243,Human_RBP_ID_23067558 RMVar_hsa_circ_128077,RMVar_hsa_circ_237931 75803 RMVar_ID_75803 Human_SNP_ID_272678746 m1A Human chr6 + 34236700 34236700 34236700 CTGCGAGGAGTGGGCGGTCGACTCGAGTTCGCAGCCCAGGCCTCCCACACGCCCCTCCCTGCCGT CTGCGAGGAGTGGGCGGTCGACTCGAGTTCGCCGCCCAGGCCTCCCACACGCCCCTCCCTGCCGT A C RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:34236546..34236715;chr6:34236622..34236705 26863196 MeRIP-seq:(Medium) rs1001086760 Functional Loss SNV dbSNP153 33..33 33 - - - 75804 RMVar_ID_75804 Human_SNP_ID_272678940 m1A Human chr6 + 34236957 34236957 34236957 CCGGGGCTATTTCTGGCGCTGGCGCGGCTCCAAGAAGGCGTGAGTTCGCGGCCGCTCCGGTGGCT CCGGGGCTATTTCTGGCGCTGGCGCGGCTCCAGGAAGGCGTGAGTTCGCGGCCGCTCCGGTGGCT A G HMGA1 Ensembl:ENSG00000137309 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:34236876..34237011;chr6:34236876..34237023 26863196 MeRIP-seq:(Medium) rs919936139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662741,Human_RBP_ID_3968995,Human_RBP_ID_4903951,Human_RBP_ID_5478703,Human_RBP_ID_18074603 Human_Splice_Rec_763233,Human_Splice_Rec_763241,Human_Splice_Rec_763251 75805 RMVar_ID_75805 Human_SNP_ID_272678942 m1A Human chr6 + 34236959 34236959 34236959 GGGGCTATTTCTGGCGCTGGCGCGGCTCCAAGAAGGCGTGAGTTCGCGGCCGCTCCGGTGGCTTC GGGGCTATTTCTGGCGCTGGCGCGGCTCCAAGGAGGCGTGAGTTCGCGGCCGCTCCGGTGGCTTC A G HMGA1 Ensembl:ENSG00000137309 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:34236926..34236975 26863196 MeRIP-seq:(Medium) rs1015025233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903951,Human_RBP_ID_5478703 Human_Splice_Rec_763233,Human_Splice_Rec_763241,Human_Splice_Rec_763251 75806 RMVar_ID_75806 Human_SNP_ID_272678943 m1A Human chr6 + 34236960 34236960 34236960 GGGCTATTTCTGGCGCTGGCGCGGCTCCAAGAAGGCGTGAGTTCGCGGCCGCTCCGGTGGCTTCT GGGCTATTTCTGGCGCTGGCGCGGCTCCAAGACGGCGTGAGTTCGCGGCCGCTCCGGTGGCTTCT A C HMGA1 Ensembl:ENSG00000137309 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:34236876..34237013;chr6:34236876..34237029;chr6:34236876..34236975;chr6:34236901..34236975 26863196,26863410,26863196,32194978 MeRIP-seq:(Medium) rs963449933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903952,Human_RBP_ID_5478703 Human_Splice_Rec_763233,Human_Splice_Rec_763241,Human_Splice_Rec_763251 75807 RMVar_ID_75807 Human_SNP_ID_272679101 m1A Human chr6 + 34237278 34237278 34237278 GGTCCTCAGCGCCCAGCACCGCCGCTCCCGGCAACCCGGAGCGCGCACCGCAGGCCGGCGGCCGA GGTCCTCAGCGCCCAGCACCGCCGCTCCCGGCCACCCGGAGCGCGCACCGCAGGCCGGCGGCCGA A C HMGA1 Ensembl:ENSG00000137309 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:34237176..34238791 32194978 MeRIP-seq:(Medium) rs949307113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81780,Human_RBP_ID_662745,Human_RBP_ID_4885605,Human_RBP_ID_18195552,Human_RBP_ID_22462015,Human_RBP_ID_22534197,Human_RBP_ID_26828412 Human_Splice_Rec_763223,Human_Splice_Rec_763225,Human_Splice_Rec_763242,Human_Splice_Rec_763243,Human_Splice_Rec_763252,Human_Splice_Rec_763253,Human_Splice_Rec_763261 RMVar_hsa_circ_52655 75808 RMVar_ID_75808 Human_SNP_ID_272679548 m1A Human chr6 - 34238183 34238183 34238183 CACCCCGACCGCATGCACCGCCACGCGGGTGCACCCGGCCCCACTTCCTGCCAGAGGGGGCACCC CACCCCGACCGCATGCACCGCCACGCGGGTGCGCCCGGCCCCACTTCCTGCCAGAGGGGGCACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34238175..34238260 26863196 MeRIP-seq:(Medium) rs972217486 Functional Loss SNV dbSNP153 33..33 33 - - - 75809 RMVar_ID_75809 Human_SNP_ID_272680434 m1A Human chr6 + 34240750 34240750 34240750 GCACTTTTCTGTCTCCCAGCATCCCAGCCATCACTCTTCCACCTGCTCCTTAGAGAAGGGAAGAT GCACTTTTCTGTCTCCCAGCATCCCAGCCATCCCTCTTCCACCTGCTCCTTAGAGAAGGGAAGAT A C HMGA1 Ensembl:ENSG00000137309 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34240726..34240750 26863196 MeRIP-seq:(Medium) rs771566300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904795,Human_RBP_ID_5217598,Human_RBP_ID_5478704 Human_Splice_Rec_763224,Human_Splice_Rec_763226,Human_Splice_Rec_763234,Human_Splice_Rec_763244,Human_Splice_Rec_763254,Human_Splice_Rec_763262,Human_Splice_Rec_763270 RMVar_hsa_circ_126239,RMVar_hsa_circ_52655,RMVar_hsa_circ_237945,RMVar_hsa_circ_321526 75810 RMVar_ID_75810 Human_SNP_ID_272680474 m1A Human chr6 - 34240879 34240879 34240879 CTCCCTACCAGCGCTGTCCCGGGACTCACCGGAGGCTGCTTGCGCGGCCTGCCCCGGCCCCGCTT CTCCCTACCAGCGCTGTCCCGGGACTCACCGGGGGCTGCTTGCGCGGCCTGCCCCGGCCCCGCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:34240692..34240933;chr6:34240682..34240952 26863196 MeRIP-seq:(Medium) rs1365434573 Functional Loss SNV dbSNP153 33..33 33 - - - 75811 RMVar_ID_75811 Human_SNP_ID_272681017 m1A Human chr6 - 34242780 34242780 34242780 CCCATCTCAAGTCTCACCCGGGTCTTGGCAGCACCCTTGTTTTTGCTTCCCTTTGGTCGGCCCCG CCCATCTCAAGTCTCACCCGGGTCTTGGCAGCGCCCTTGTTTTTGCTTCCCTTTGGTCGGCCCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:34242751..34242800 26863196 MeRIP-seq:(Medium) rs1207411040 Functional Loss SNV dbSNP153 33..33 33 - - - 75812 RMVar_ID_75812 Human_SNP_ID_272681257 m1A Human chr6 - 34243517 34243517 34243517 GAGGCAAGCAGCAGTCTGCTTCTTCACCTACCAGTTTTTTGGGTCTGCCCCTTGGTTTCCTTCCT GAGGCAAGCAGCAGTCTGCTTCTTCACCTACCCGTTTTTTGGGTCTGCCCCTTGGTTTCCTTCCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:34243451..34243525 32194978 MeRIP-seq:(Medium) rs866916508 Functional Loss SNV dbSNP153 33..33 33 - - - 75813 RMVar_ID_75813 Human_SNP_ID_272681755 m1A Human chr6 - 34244923 34244920 34244924 GGAGCGGAGCAAAGCTGTCCAGTCCCAGAAGGAAGCTGCTCCTCCAGTGAGGAGCAGGCGGCACG GGAGCGGAGCAAAGCTGTCCAGTCCCAGAAG____CTGCTCCTCCAGTGAGGAGCAGGCGGCACG GCTTC G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:34244876..34245060 26863196 MeRIP-seq:(Medium) rs772826618 Functional Loss DEL dbSNP153 32..35 33 - - - 75814 RMVar_ID_75814 Human_SNP_ID_272681838 m1A Human chr6 + 34245033 34245033 34245033 GGCCGCCACCCCCATCTTCCACCTGTGCCCTCACCACCACACTACACAGCACACCAGCCGCTGCA GGCCGCCACCCCCATCTTCCACCTGTGCCCTCGCCACCACACTACACAGCACACCAGCCGCTGCA A G HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:34244911..34245050 26863196 MeRIP-seq:(Medium) rs1248470113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170018,Human_RBP_ID_17310215,Human_RBP_ID_17419820,Human_RBP_ID_17537877,Human_RBP_ID_17664057,Human_RBP_ID_18195558,Human_RBP_ID_18957320,Human_RBP_ID_21221756,Human_RBP_ID_22534097,Human_RBP_ID_27524126 Human_miRNA_ID_191320,Human_miRNA_ID_2061277 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 75815 RMVar_ID_75815 Human_SNP_ID_272681839 m1A Human chr6 + 34245036 34245036 34245036 CGCCACCCCCATCTTCCACCTGTGCCCTCACCACCACACTACACAGCACACCAGCCGCTGCAGGG CGCCACCCCCATCTTCCACCTGTGCCCTCACCTCCACACTACACAGCACACCAGCCGCTGCAGGG A T HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:34240688..34245299 26863196 MeRIP-seq:(Medium) rs757264395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170018,Human_RBP_ID_17310215,Human_RBP_ID_17419820,Human_RBP_ID_17537878,Human_RBP_ID_17664057,Human_RBP_ID_18195558,Human_RBP_ID_18957320,Human_RBP_ID_21221756,Human_RBP_ID_22534097,Human_RBP_ID_27524126 Human_miRNA_ID_2051040,Human_miRNA_ID_2061277 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 75816 RMVar_ID_75816 Human_SNP_ID_272681841 m1A Human chr6 + 34245039 34245037 34245039 CACCCCCATCTTCCACCTGTGCCCTCACCACCACACTACACAGCACACCAGCCGCTGCAGGGCTC CACCCCCATCTTCCACCTGTGCCCTCACCAC__CACTACACAGCACACCAGCCGCTGCAGGGCTC CCA C HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:34244774..34245290 26863196 MeRIP-seq:(Medium) rs1561878307 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_170018,Human_RBP_ID_17310215,Human_RBP_ID_17419820,Human_RBP_ID_17537878,Human_RBP_ID_17664057,Human_RBP_ID_18195558,Human_RBP_ID_18957320,Human_RBP_ID_21221756,Human_RBP_ID_22534097,Human_RBP_ID_27524126 Human_miRNA_ID_292696,Human_miRNA_ID_2051040,Human_miRNA_ID_2061277 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 75817 RMVar_ID_75817 Human_SNP_ID_272681859 m1A Human chr6 - 34245080 34245080 34245080 AACTGAGGCCAGGGGAAAACTGCTCCCCACTCAGCCCATGGGAGCCCTGCAGCGGCTGGTGTGCT AACTGAGGCCAGGGGAAAACTGCTCCCCACTCGGCCCATGGGAGCCCTGCAGCGGCTGGTGTGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:34245076..34245100 26863196 MeRIP-seq:(Medium) rs1468144180 Functional Loss SNV dbSNP153 33..33 33 - - - 75818 RMVar_ID_75818 Human_SNP_ID_272681929 m1A Human chr6 + 34245206 34245206 34245206 ACTTAGCCGCACCCTGCACCTGCTGCGTCCCCACTCCCTTGGTGGTGGGGACATTGCTCTCTGGG ACTTAGCCGCACCCTGCACCTGCTGCGTCCCCTCTCCCTTGGTGGTGGGGACATTGCTCTCTGGG A T HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34245156..34245286 26863196 MeRIP-seq:(Medium) rs962169002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662758,Human_RBP_ID_790407,Human_RBP_ID_1217470,Human_RBP_ID_17091451,Human_RBP_ID_17306787,Human_RBP_ID_17421609,Human_RBP_ID_17537879,Human_RBP_ID_18074614,Human_RBP_ID_21221757,Human_RBP_ID_27161171,Human_RBP_ID_27527021 Human_miRNA_ID_96891,Human_miRNA_ID_1421218,Human_miRNA_ID_2725207 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 75819 RMVar_ID_75819 Human_SNP_ID_272682129 m1A Human chr6 - 34245608 34245608 34245608 TGGACAATAAGTGACTGCATCTCCATCACCACAATATGTACTCAGATCCCAGGCGGAGGGCAAGG TGGACAATAAGTGACTGCATCTCCATCACCACGATATGTACTCAGATCCCAGGCGGAGGGCAAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34245558..34245684 26863196 MeRIP-seq:(Medium) rs1271161001 Functional Loss SNV dbSNP153 33..33 33 - - - 75820 RMVar_ID_75820 Human_SNP_ID_272682151 m1A Human chr6 + 34245669 34245669 34245669 TCCAGGTGAGGCCCAAGAGCCCTGTGGCCGCCACCTGAGGTGGGCTGGGGCTGCTCCCCTAACCC TCCAGGTGAGGCCCAAGAGCCCTGTGGCCGCCGCCTGAGGTGGGCTGGGGCTGCTCCCCTAACCC A G HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:34245659..34245930;chr6:34245401..34246025;chr6:34245401..34246175 26863196,32194978,32194978 MeRIP-seq:(Medium) rs144540283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251601,Human_RBP_ID_671347,Human_RBP_ID_790412,Human_RBP_ID_5134128,Human_RBP_ID_17421620,Human_RBP_ID_18084804,Human_RBP_ID_18195565,Human_RBP_ID_18958267 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 75821 RMVar_ID_75821 Human_SNP_ID_272682524 m1A Human chr6 + 34246726 34246706 34246726 GAGACCCAGCACCCAGCAGGGGGAGCCAGGTGACAGCAGGGGAAGCAGATGGCAGGGCCCCAGGC GAGACCCAGCACC____________________CAGCAGGGGAAGCAGATGGCAGGGCCCCAGGC CCAGCAGGGGGAGCCAGGTGA C RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:34246676..34246875 32194978 MeRIP-seq:(Medium) rs771841146 Functional Loss DEL dbSNP153 14..33 33 - - - 75822 RMVar_ID_75822 Human_SNP_ID_272687447 m1A Human chr6 - 34263420 34263420 34263420 CAGGAACTACAAGCCCCTGGACCTGCGGCCTAAGAAGACACGCGCCATGCGCCGCCGGCTCAACA CAGGAACTACAAGCCCCTGGACCTGCGGCCTAGGAAGACACGCGCCATGCGCCGCCGGCTCAACA T C RPL35P2 Ensembl:ENSG00000220583 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34263418..34263512 26863196 MeRIP-seq:(Medium) rs1395854156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5104234,Human_RBP_ID_17422745 Human_miRNA_ID_1823272,Human_miRNA_ID_1834533,Human_miRNA_ID_1901199 75823 RMVar_ID_75823 Human_SNP_ID_272691731 m1A Human chr6 - 34280059 34280059 34280059 ACAGTCAGGCTGTGGAGGAGGGCTGAGAAGAAAGGGGCACTGGTCCAGCCCCAGGTTTGGTCTGA ACAGTCAGGCTGTGGAGGAGGGCTGAGAAGAAGGGGGCACTGGTCCAGCCCCAGGTTTGGTCTGA T C NUDT3 Ensembl:ENSG00000272325 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:34279870..34280177 32194978 MeRIP-seq:(Medium) rs1002627091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7595268,Human_RBP_ID_15793961,Human_RBP_ID_21991118 75824 RMVar_ID_75824 Human_SNP_ID_272692003 m1A Human chr6 - 34281309 34281309 34281309 AGTAGCATCTTCATACTTACTTTTGCCAGCCCAGCCTCCATTTCAAAGACTTTGTCTTCCATCCT AGTAGCATCTTCATACTTACTTTTGCCAGCCCGGCCTCCATTTCAAAGACTTTGTCTTCCATCCT T C NUDT3 Ensembl:ENSG00000272325 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:34281260..34282102 32194978 MeRIP-seq:(Medium) rs1042159476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26828417,Human_RBP_ID_27755127 75825 RMVar_ID_75825 Human_SNP_ID_272719373 m1A Human chr6 - 34392271 34392271 34392271 GGCCGCATGCCTGTGTTTCCGCAGCGAGAGCGAGGAGGAGGTGAGGCGGCAGGCTGGGCGGGCCG GGCCGCATGCCTGTGTTTCCGCAGCGAGAGCGGGGAGGAGGTGAGGCGGCAGGCTGGGCGGGCCG T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:34392251..34392275 26863196 MeRIP-seq:(Medium) rs1377172787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8905785,Human_RBP_ID_23067714 Human_Splice_Rec_763349 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 75826 RMVar_ID_75826 Human_SNP_ID_272728784 m1A Human chr6 - 34425161 34425161 34425161 CCATTTATGAACTCCTTTTTAAGGAGGGAGTCATGGTGGCCAAGAAGGATGTCCACATGCCTAAG CCATTTATGAACTCCTTTTTAAGGAGGGAGTCGTGGTGGCCAAGAAGGATGTCCACATGCCTAAG T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:34425099..34425823 26863410 MeRIP-seq:(Medium) rs1452621781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5122235,Human_RBP_ID_9400418 Human_Splice_Rec_763358,Human_Splice_Rec_763359,Human_Splice_Rec_763374,Human_Splice_Rec_763375,Human_Splice_Rec_763389,Human_Splice_Rec_763402,Human_Splice_Rec_763403,Human_Splice_Rec_763408,Human_Splice_Rec_763409,Human_Splice_Rec_763418,Human_Splice_Rec_763419,Human_Splice_Rec_763428,Human_Splice_Rec_763429,Human_Splice_Rec_763438,Human_Splice_Rec_763439,Human_Splice_Rec_763450,Human_Splice_Rec_763451,Human_Splice_Rec_763458,Human_Splice_Rec_763459,Human_Splice_Rec_763468,Human_Splice_Rec_763469,Human_Splice_Rec_763478,Human_Splice_Rec_763479 Human_miRNA_ID_2674558,Human_miRNA_ID_2674559,Human_miRNA_ID_2925309,Human_miRNA_ID_2925310 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 75827 RMVar_ID_75827 Human_SNP_ID_272728785 m1A Human chr6 - 34425161 34425161 34425161 CCATTTATGAACTCCTTTTTAAGGAGGGAGTCATGGTGGCCAAGAAGGATGTCCACATGCCTAAG CCATTTATGAACTCCTTTTTAAGGAGGGAGTCCTGGTGGCCAAGAAGGATGTCCACATGCCTAAG T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:34425099..34425823 26863410 MeRIP-seq:(Medium) rs1452621781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5122235,Human_RBP_ID_9400418 Human_Splice_Rec_763358,Human_Splice_Rec_763359,Human_Splice_Rec_763374,Human_Splice_Rec_763375,Human_Splice_Rec_763389,Human_Splice_Rec_763402,Human_Splice_Rec_763403,Human_Splice_Rec_763408,Human_Splice_Rec_763409,Human_Splice_Rec_763418,Human_Splice_Rec_763419,Human_Splice_Rec_763428,Human_Splice_Rec_763429,Human_Splice_Rec_763438,Human_Splice_Rec_763439,Human_Splice_Rec_763450,Human_Splice_Rec_763451,Human_Splice_Rec_763458,Human_Splice_Rec_763459,Human_Splice_Rec_763468,Human_Splice_Rec_763469,Human_Splice_Rec_763478,Human_Splice_Rec_763479 Human_miRNA_ID_2674558,Human_miRNA_ID_2674559,Human_miRNA_ID_2925309,Human_miRNA_ID_2925310 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 75828 RMVar_ID_75828 Human_SNP_ID_272729053 m1A Human chr6 - 34425918 34425918 34425918 CGGGCAGGGGGCCTCTCTCCCACTCCCCACACACCGATTTCTGAGTAGCGATAGGGGCTGGAGGC CGGGCAGGGGGCCTCTCTCCCACTCCCCACACGCCGATTTCTGAGTAGCGATAGGGGCTGGAGGC T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34425914..34426075 26863196 MeRIP-seq:(Medium) rs1010411295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 75829 RMVar_ID_75829 Human_SNP_ID_272729054 m1A Human chr6 - 34425920 34425920 34425920 TGCGGGCAGGGGGCCTCTCTCCCACTCCCCACACACCGATTTCTGAGTAGCGATAGGGGCTGGAG TGCGGGCAGGGGGCCTCTCTCCCACTCCCCACGCACCGATTTCTGAGTAGCGATAGGGGCTGGAG T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:34425918..34426100 26863196 MeRIP-seq:(Medium) rs1269762007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 75830 RMVar_ID_75830 Human_SNP_ID_272729056 m1A Human chr6 - 34425929 34425929 34425929 TCCCCAGGATGCGGGCAGGGGGCCTCTCTCCCACTCCCCACACACCGATTTCTGAGTAGCGATAG TCCCCAGGATGCGGGCAGGGGGCCTCTCTCCCCCTCCCCACACACCGATTTCTGAGTAGCGATAG T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding 5'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:34425927..34426025 32194978 MeRIP-seq:(Medium) rs1326759400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 75831 RMVar_ID_75831 Human_SNP_ID_272770127 m1A Human chr6 - 34588377 34588377 34588377 ACCCCTGCTTTCCTGACTTCCTCTTCTGCCCAACACTGGGTGCCCCTTCCCAGTTTCCCAGCAGG ACCCCTGCTTTCCTGACTTCCTCTTCTGCCCAGCACTGGGTGCCCCTTCCCAGTTTCCCAGCAGG T C ILRUN Ensembl:ENSG00000196821 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:34588326..34588575 32194978 MeRIP-seq:(Medium) rs1052858075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790633,Human_RBP_ID_1047231,Human_RBP_ID_17090874,Human_RBP_ID_17421637,Human_RBP_ID_18958278,Human_RBP_ID_27524164 Human_miRNA_ID_506872,Human_miRNA_ID_514071,Human_miRNA_ID_2174785,Human_miRNA_ID_2178228,Human_miRNA_ID_2384129 RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960 75832 RMVar_ID_75832 Human_SNP_ID_272770215 m1A Human chr6 - 34588826 34588826 34588826 ACTGTTGTTTTTTTAGAGCTTGATTGTGGGAGAAAAGCTTGTGTGAAATTCCCTCTTCACCTCCC ACTGTTGTTTTTTTAGAGCTTGATTGTGGGAGGAAAGCTTGTGTGAAATTCCCTCTTCACCTCCC T C ILRUN Ensembl:ENSG00000196821 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:34588776..34588850 32194978 MeRIP-seq:(Medium) rs935572801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663028,Human_RBP_ID_1069594,Human_RBP_ID_2019605,Human_RBP_ID_3807354,Human_RBP_ID_5152155,Human_RBP_ID_5304248,Human_RBP_ID_7596846,Human_RBP_ID_8216481,Human_RBP_ID_15798845,Human_RBP_ID_24159234,Human_RBP_ID_26539262 Human_miRNA_ID_2539196,Human_miRNA_ID_2867552 RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960 75833 RMVar_ID_75833 Human_SNP_ID_272772580 m1A Human chr6 + 34599836 34599836 34599836 ATGGAACCCTGTTCTCTCCCCACTTCTACTGCATCCTTTCCCCTATCCATTGATGGTAGCTCCAT ATGGAACCCTGTTCTCTCCCCACTTCTACTGCGTCCTTTCCCCTATCCATTGATGGTAGCTCCAT A G RF00017-4751 RNACentral:URS000099F4EE SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34599833..34599962 26863196 MeRIP-seq:(Medium) rs1343694018 Functional Loss SNV dbSNP153 33..33 33 - - - 75834 RMVar_ID_75834 Human_SNP_ID_272796962 m1A Human chr6 + 34695632 34695632 34695632 GCTTTCTTTCAGATAAGCCCCTCTCCATTCCCAGCATTCTGGTGACCCCAGATGAACCCTCTGCC GCTTTCTTTCAGATAAGCCCCTCTCCATTCCCGGCATTCTGGTGACCCCAGATGAACCCTCTGCC A G RF00017-4751,RF00017-1033 RNACentral:URS000099F4EE,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34695630..34695794 26863196 MeRIP-seq:(Medium) rs1394155166 Functional Loss SNV dbSNP153 33..33 33 - - - 75835 RMVar_ID_75835 Human_SNP_ID_272797240 m1A Human chr6 + 34696741 34696741 34696741 CCCGCTCCTTTGAGGTAGGCCCCGGGCCTCTCACAGTCTCATAGGGGTAAACTCACTCTGCCACT CCCGCTCCTTTGAGGTAGGCCCCGGGCCTCTCCCAGTCTCATAGGGGTAAACTCACTCTGCCACT A C AL451165.2 Ensembl:ENSG00000272288 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr6:34696574..34696800;chr6:34696505..34697181 26863196 MeRIP-seq:(Medium) rs1325854611 Functional Loss SNV dbSNP153 33..33 33 - - - 75836 RMVar_ID_75836 Human_SNP_ID_272813597 m1A Human chr6 + 34762556 34762556 34762556 GGTAAAACTTTATTAAATTTTTAGTGTTGGACATTTGTTTCTACGTCTGATATGATCTTTTTATT GGTAAAACTTTATTAAATTTTTAGTGTTGGACGTTTGTTTCTACGTCTGATATGATCTTTTTATT A G SNRPC Ensembl:ENSG00000124562 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:34762554..34762736 26863196 MeRIP-seq:(Medium) rs752746512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22553736,Human_RBP_ID_22682764 RMVar_hsa_circ_47598 75837 RMVar_ID_75837 Human_SNP_ID_272821204 m1A Human chr6 - 34792142 34792142 34792142 CCTCACCTCGCCGCGGCGTGAGCACCGGACACAGCCGCCGCCGCCGCCATGGCGCTTTCTCGCCC CCTCACCTCGCCGCGGCGTGAGCACCGGACACCGCCGCCGCCGCCGCCATGGCGCTTTCTCGCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34792002..34792578 26863196 MeRIP-seq:(Medium) rs1554123801 Functional Loss SNV dbSNP153 33..33 33 - - - 75838 RMVar_ID_75838 Human_SNP_ID_272821210 m1A Human chr6 - 34792151 34792151 34792151 AGGCGGTCCCCTCACCTCGCCGCGGCGTGAGCACCGGACACAGCCGCCGCCGCCGCCATGGCGCT AGGCGGTCCCCTCACCTCGCCGCGGCGTGAGCGCCGGACACAGCCGCCGCCGCCGCCATGGCGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34792014..34792263 26863196 MeRIP-seq:(Medium) rs1466610510 Functional Loss SNV dbSNP153 33..33 33 - - - 75839 RMVar_ID_75839 Human_SNP_ID_272821228 m1A Human chr6 + 34792220 34792220 34792220 TCCACAACTGAGGAGGCCACAGCTGCCGGCCCACCCGCCTTCCACGCGGGCCGCGGCTCCGGCAT TCCACAACTGAGGAGGCCACAGCTGCCGGCCCCCCCGCCTTCCACGCGGGCCGCGGCTCCGGCAT A C UHRF1BP1 Ensembl:ENSG00000065060 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:34792122..34792242 26863410 MeRIP-seq:(Medium) rs1412144266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903973,Human_RBP_ID_8905334,Human_RBP_ID_26764379,Human_RBP_ID_26829586 Human_Splice_Rec_763651,Human_Splice_Rec_763691 75840 RMVar_ID_75840 Human_SNP_ID_272821277 m1A Human chr6 - 34792327 34792327 34792327 GGGAGGAGGTCGGAGAGGGTTAGGAAGGGCCCAGGACCGCCGGGGGCCGGCGCTGGCGCTCTCAC GGGAGGAGGTCGGAGAGGGTTAGGAAGGGCCCGGGACCGCCGGGGGCCGGCGCTGGCGCTCTCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34792318..34792850 26863196 MeRIP-seq:(Medium) rs1016774628 Functional Loss SNV dbSNP153 33..33 33 - - - 75841 RMVar_ID_75841 Human_SNP_ID_272821280 m1A Human chr6 - 34792334 34792334 34792334 GGCGTCAGGGAGGAGGTCGGAGAGGGTTAGGAAGGGCCCAGGACCGCCGGGGGCCGGCGCTGGCG GGCGTCAGGGAGGAGGTCGGAGAGGGTTAGGAGGGGCCCAGGACCGCCGGGGGCCGGCGCTGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34792327..34792541 26863196 MeRIP-seq:(Medium) rs1342179815 Functional Loss SNV dbSNP153 33..33 33 - - - 75842 RMVar_ID_75842 Human_SNP_ID_272821281 m1A Human chr6 - 34792334 34792334 34792334 GGCGTCAGGGAGGAGGTCGGAGAGGGTTAGGAAGGGCCCAGGACCGCCGGGGGCCGGCGCTGGCG GGCGTCAGGGAGGAGGTCGGAGAGGGTTAGGACGGGCCCAGGACCGCCGGGGGCCGGCGCTGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34792327..34792541 26863196 MeRIP-seq:(Medium) rs1342179815 Functional Loss SNV dbSNP153 33..33 33 - - - 75843 RMVar_ID_75843 Human_SNP_ID_272843672 m1A Human chr6 - 34887836 34887836 34887836 TACCGACACCGATGGAATCCCAGAGGAAACTGACGGAGACGCAGATGTGGACTTGAAAGAAGCTG TACCGACACCGATGGAATCCCAGAGGAAACTGTCGGAGACGCAGATGTGGACTTGAAAGAAGCTG T A TAF11 Ensembl:ENSG00000064995 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34887776..34888000 26863196 MeRIP-seq:(Medium) rs770574763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663173,Human_RBP_ID_951801,Human_RBP_ID_1395324,Human_RBP_ID_2019724,Human_RBP_ID_9402005,Human_RBP_ID_15801365,Human_RBP_ID_19018435 Human_Splice_Rec_763731,Human_Splice_Rec_763741,Human_Splice_Rec_763749 Human_miRNA_ID_2245261 RMVar_hsa_circ_89116,RMVar_hsa_circ_237992 75844 RMVar_ID_75844 Human_SNP_ID_272843682 m1A Human chr6 - 34887867 34887867 34887867 AGACGGCCGCTGTGCCCGGGGACCCGGGGGCTACCGACACCGATGGAATCCCAGAGGAAACTGAC AGACGGCCGCTGTGCCCGGGGACCCGGGGGCTGCCGACACCGATGGAATCCCAGAGGAAACTGAC T C TAF11 Ensembl:ENSG00000064995 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:34887825..34887961 26863196 MeRIP-seq:(Medium) rs1459613752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2019724,Human_RBP_ID_4903974,Human_RBP_ID_23067819 Human_Splice_Rec_763731,Human_Splice_Rec_763741,Human_Splice_Rec_763749 RMVar_hsa_circ_89116,RMVar_hsa_circ_237992 75845 RMVar_ID_75845 Human_SNP_ID_272868735 m1A Human chr6 + 34999895 34999892 34999896 AGAGACAAAGAAGGAGTCAAGAAAAGAGAAAGAGAGACAGAGAAAGAGAGAGGCAGAAAGAGGAA AGAGACAAAGAAGGAGTCAAGAAAAGAGAA____AGACAGAGAAAGAGAGAGGCAGAAAGAGGAA AAGAG A ANKS1A Ensembl:ENSG00000064999 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34999844..34999971 26863196 MeRIP-seq:(Medium) rs1233126013 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_103723,RMVar_hsa_circ_237993,RMVar_hsa_circ_119774,RMVar_hsa_circ_377188,RMVar_hsa_circ_237994,RMVar_hsa_circ_61071,RMVar_hsa_circ_237999,RMVar_hsa_circ_81918,RMVar_hsa_circ_238000,RMVar_hsa_circ_74299,RMVar_hsa_circ_26471,RMVar_hsa_circ_336218,RMVar_hsa_circ_366216 75846 RMVar_ID_75846 Human_SNP_ID_272917785 m1A Human chr6 - 35217269 35217269 35217269 TGCGAGGATTAGGTCTTTTTAACCACTGCTGCACACACCCCCCCCCCCGCCGCGCCTCCCCCCCG TGCGAGGATTAGGTCTTTTTAACCACTGCTGCCCACACCCCCCCCCCCGCCGCGCCTCCCCCCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:35217136..35217275 26863196 MeRIP-seq:(Medium) rs1355239932 Functional Loss SNV dbSNP153 33..33 33 - - - 75847 RMVar_ID_75847 Human_SNP_ID_272921232 m1A Human chr6 - 35233885 35233880 35233885 GCATCTGGAGGAGAGAGAAGGAAATGGGGGGTAAGGTGAGGTGAGTAGAAAGGGGAGTTGCAGGA GCATCTGGAGGAGAGAGAAGGAAATGGGGGGT_____GAGGTGAGTAGAAAGGGGAGTTGCAGGA CACCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:35233836..35234003 26863196 MeRIP-seq:(Medium) rs1304083869 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_7598275 75848 RMVar_ID_75848 Human_SNP_ID_272922355 m1A Human chr6 - 35239168 35239168 35239168 GCTGGGTAGCTGATGGGGGAGGGCTGGGGGCCAGGCAAGGGGCTGGACTGGGAGAGATCTGGAGA GCTGGGTAGCTGATGGGGGAGGGCTGGGGGCCGGGCAAGGGGCTGGACTGGGAGAGATCTGGAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:35239073..35239302 26863196 MeRIP-seq:(Medium) rs1430302486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7598296 75849 RMVar_ID_75849 Human_SNP_ID_272922362 m1A Human chr6 + 35239198 35239198 35239198 CCTGGCCCCCAGCCCTCCCCCATCAGCTACCCAGCCTCACTGGCTCTCCTGGAGGTCCTCCCTGC CCTGGCCCCCAGCCCTCCCCCATCAGCTACCCGGCCTCACTGGCTCTCCTGGAGGTCCTCCCTGC A G SCUBE3 Ensembl:ENSG00000146197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35239100..35239262 26863196 MeRIP-seq:(Medium) rs535301301 Functional Loss SNV dbSNP153 33..33 33 - - - 75850 RMVar_ID_75850 Human_SNP_ID_272927350 m1A Human chr6 - 35259771 35259771 35259771 ATGCACCGGGCCCCGCCACCAGCGCCGGCCCCACAACCCGCCTGCGCCATAGCCCGCCCGCCCGC ATGCACCGGGCCCCGCCACCAGCGCCGGCCCCGCAACCCGCCTGCGCCATAGCCCGCCCGCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr6:35259726..35259874;chr6:35259538..35259891;chr6:35259726..35260009 26863196 MeRIP-seq:(Medium) rs1167913283 Functional Loss SNV dbSNP153 33..33 33 - - - 75851 RMVar_ID_75851 Human_SNP_ID_272927351 m1A Human chr6 - 35259771 35259771 35259771 ATGCACCGGGCCCCGCCACCAGCGCCGGCCCCACAACCCGCCTGCGCCATAGCCCGCCCGCCCGC ATGCACCGGGCCCCGCCACCAGCGCCGGCCCCCCAACCCGCCTGCGCCATAGCCCGCCCGCCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr6:35259726..35259874;chr6:35259538..35259891;chr6:35259726..35260009 26863196 MeRIP-seq:(Medium) rs1167913283 Functional Loss SNV dbSNP153 33..33 33 - - - 75852 RMVar_ID_75852 Human_SNP_ID_272936564 m1A Human chr6 + 35295536 35295536 35295536 CTCAAAATCAGCTGGGCGCCCACTCTCCTCCTAAAGAACACCCTTCTGGCCCTCAGTCTGTTCCC CTCAAAATCAGCTGGGCGCCCACTCTCCTCCTGAAGAACACCCTTCTGGCCCTCAGTCTGTTCCC A G ZNF76 Ensembl:ENSG00000065029 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35295485..35295686 32194978 MeRIP-seq:(Medium) rs1446106328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18075181 Human_miRNA_ID_2661614,Human_miRNA_ID_2680061 RMVar_hsa_circ_238032,RMVar_hsa_circ_116624 75853 RMVar_ID_75853 Human_SNP_ID_272942484 m1A Human chr6 - 35321252 35321252 35321252 GGATCCCCAGCGGGTCAGGCGCTTTAGGGAGGAGTCACGGTGGGCAAGCAGAGGGGGCTGGAAGC GGATCCCCAGCGGGTCAGGCGCTTTAGGGAGGTGTCACGGTGGGCAAGCAGAGGGGGCTGGAAGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35317892..35321372 32194978 MeRIP-seq:(Medium) rs1456796453 Functional Loss SNV dbSNP153 33..33 33 - - - 75854 RMVar_ID_75854 Human_SNP_ID_272947550 m1A Human chr6 + 35342648 35342648 35342648 CAGGAGCGGGAGAATTCTGCGGAGCCTGCGGGACGGCGGCGGTGGCGCCGTAGGCAGCCGGGACA CAGGAGCGGGAGAATTCTGCGGAGCCTGCGGGGCGGCGGCGGTGGCGCCGTAGGCAGCCGGGACA A G PPARD Ensembl:ENSG00000112033 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:35342603..35342734;chr6:35342576..35342790;chr6:35342554..35342789 26863196 MeRIP-seq:(Medium) rs1265301125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951161,Human_RBP_ID_9336122,Human_RBP_ID_18425418,Human_RBP_ID_19018448,Human_RBP_ID_22105016,Human_RBP_ID_23067352,Human_RBP_ID_26792409 Human_Splice_Rec_764431,Human_Splice_Rec_764445,Human_Splice_Rec_764455,Human_Splice_Rec_764467,Human_Splice_Rec_764481 RMVar_hsa_circ_87246,RMVar_hsa_circ_238048 75855 RMVar_ID_75855 Human_SNP_ID_272948604 m1A Human chr6 + 35347091 35347091 35347091 TCCTGCAGTGTTGTACAGTGTTTTGGGCATGCACGTGATACTCACACAGTGGCTTCTGCTCACCA TCCTGCAGTGTTGTACAGTGTTTTGGGCATGCCCGTGATACTCACACAGTGGCTTCTGCTCACCA A C PPARD Ensembl:ENSG00000112033 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35342656..35347141 32194978 MeRIP-seq:(Medium) rs9658070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4886708,Human_RBP_ID_8643832,Human_RBP_ID_15804089,Human_RBP_ID_18864491,Human_RBP_ID_27827593 Human_Splice_Rec_764432,Human_Splice_Rec_764433,Human_Splice_Rec_764446,Human_Splice_Rec_764447,Human_Splice_Rec_764456,Human_Splice_Rec_764457,Human_Splice_Rec_764468,Human_Splice_Rec_764469,Human_Splice_Rec_764482,Human_Splice_Rec_764483 RMVar_hsa_circ_87246,RMVar_hsa_circ_238048 75856 RMVar_ID_75856 Human_SNP_ID_272948605 m1A Human chr6 + 35347091 35347091 35347091 TCCTGCAGTGTTGTACAGTGTTTTGGGCATGCACGTGATACTCACACAGTGGCTTCTGCTCACCA TCCTGCAGTGTTGTACAGTGTTTTGGGCATGCTCGTGATACTCACACAGTGGCTTCTGCTCACCA A T PPARD Ensembl:ENSG00000112033 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35342656..35347141 32194978 MeRIP-seq:(Medium) rs9658070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4886708,Human_RBP_ID_8643832,Human_RBP_ID_15804089,Human_RBP_ID_18864491,Human_RBP_ID_27827593 Human_Splice_Rec_764432,Human_Splice_Rec_764433,Human_Splice_Rec_764446,Human_Splice_Rec_764447,Human_Splice_Rec_764456,Human_Splice_Rec_764457,Human_Splice_Rec_764468,Human_Splice_Rec_764469,Human_Splice_Rec_764482,Human_Splice_Rec_764483 RMVar_hsa_circ_87246,RMVar_hsa_circ_238048 75857 RMVar_ID_75857 Human_SNP_ID_272953297 m1A Human chr6 - 35367104 35367104 35367104 AGGTTCAAAGAATCAACCTCTTACACTCCTCCATTTCCTTTTAGCATCCAGGGAACGGACAAAAC AGGTTCAAAGAATCAACCTCTTACACTCCTCCGTTTCCTTTTAGCATCCAGGGAACGGACAAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35367098..35367206 26863196 MeRIP-seq:(Medium) rs149987507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7598465 75858 RMVar_ID_75858 Human_SNP_ID_272956779 m1A Human chr6 - 35383051 35383051 35383051 TCCTGTCAGTGACATTTCTAAGCCCAGCCATGACCTGTCACACCCTTGCCCACAAAATCCAACTC TCCTGTCAGTGACATTTCTAAGCCCAGCCATGCCCTGTCACACCCTTGCCCACAAAATCCAACTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35383049..35383150 26863196 MeRIP-seq:(Medium) rs1220275895 Functional Loss SNV dbSNP153 33..33 33 - - - 75859 RMVar_ID_75859 Human_SNP_ID_272960908 m1A Human chr6 + 35398275 35398275 35398275 AGCCAGTTAGGAGGCTGTTAAGTAATCCAGGCAGGAGATGGTGTTGGCTGGGACCAGGGTCATAG AGCCAGTTAGGAGGCTGTTAAGTAATCCAGGCGGGAGATGGTGTTGGCTGGGACCAGGGTCATAG A G PPARD Ensembl:ENSG00000112033 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:35398272..35398355 26863196 MeRIP-seq:(Medium) rs1484454954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6422 75860 RMVar_ID_75860 Human_SNP_ID_272967643 m1A Human chr6 + 35426141 35426141 35426141 CAATGGGGCCAGCACTGGAGGGGCCCACCCACATGACTTTTCCATTGACCAGCCCTTGAGCACCC CAATGGGGCCAGCACTGGAGGGGCCCACCCACGTGACTTTTCCATTGACCAGCCCTTGAGCACCC A G PPARD Ensembl:ENSG00000112033 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:35426090..35426261 26863196 MeRIP-seq:(Medium) rs199596386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27346551 75861 RMVar_ID_75861 Human_SNP_ID_272967651 m1A Human chr6 + 35426170 35426170 35426170 CACATGACTTTTCCATTGACCAGCCCTTGAGCACCCGGCCTGGAGCAGCAGAGTCCCACGATCGC CACATGACTTTTCCATTGACCAGCCCTTGAGCGCCCGGCCTGGAGCAGCAGAGTCCCACGATCGC A G PPARD Ensembl:ENSG00000112033 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35426122..35426317 26863196 MeRIP-seq:(Medium) rs368703665 Functional Loss SNV dbSNP153 33..33 33 - - - 75862 RMVar_ID_75862 Human_SNP_ID_272974258 m1A Human chr6 + 35452754 35452754 35452754 CTGGGGTCGCTTGCTCGAGGCCCTGTGCCGGGAGGAGCCGGTCGTGCAGGGGCCTGACGGCCGTC CTGGGGTCGCTTGCTCGAGGCCCTGTGCCGGGGGGAGCCGGTCGTGCAGGGGCCTGACGGCCGTC A G FANCE Ensembl:ENSG00000112039 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35452703..35452823 26863196 MeRIP-seq:(Medium) rs1046737417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17710694 Human_Splice_Rec_764505,Human_Splice_Rec_764523 75863 RMVar_ID_75863 Human_SNP_ID_272978558 m1A Human chr6 + 35469006 35469006 35469006 CAGCTTGAAGAACTATGATCCCCAGAAGGACAAGCGCTTCTCGGGCACCGTCAGGTTGGCACCGT CAGCTTGAAGAACTATGATCCCCAGAAGGACAGGCGCTTCTCGGGCACCGTCAGGTTGGCACCGT A G RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs764941115 Functional Loss SNV dbSNP153 33..33 33 - - - 75864 RMVar_ID_75864 Human_SNP_ID_272978713 m1A Human chr6 - 35469402 35469402 35469402 TGCTGGTCCCCCAGGACACACACAGAGAACTTAGGGCGGGGAGTGGACTTAAGCCTGCGTTTTGG TGCTGGTCCCCCAGGACACACACAGAGAACTTTGGGCGGGGAGTGGACTTAAGCCTGCGTTTTGG T A RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35469375..35470375 32194978 MeRIP-seq:(Medium) rs1561799714 Functional Loss SNV dbSNP153 33..33 33 - - - 75865 RMVar_ID_75865 Human_SNP_ID_272979002 m1A Human chr6 + 35470264 35470264 35470264 CGAATCCTCGGCCCAGGTTTAAATAAGGCAGGAAAGTTCCCTTCCCTGCTCACACACAACGAAAA CGAATCCTCGGCCCAGGTTTAAATAAGGCAGGCAAGTTCCCTTCCCTGCTCACACACAACGAAAA A C RPL10A Ensembl:ENSG00000198755 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:35470214..35470355 26863196 MeRIP-seq:(Medium) rs759383989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663335,Human_RBP_ID_1395359,Human_RBP_ID_7598568,Human_RBP_ID_9193955,Human_RBP_ID_17306929,Human_RBP_ID_17421657,Human_RBP_ID_24160035 Human_Splice_Rec_764550,Human_Splice_Rec_764551,Human_Splice_Rec_764558,Human_Splice_Rec_764559,Human_Splice_Rec_764566,Human_Splice_Rec_764567,Human_Splice_Rec_764574,Human_Splice_Rec_764575,Human_Splice_Rec_764584,Human_Splice_Rec_764585 RMVar_hsa_circ_96266,RMVar_hsa_circ_88658,RMVar_hsa_circ_115289,RMVar_hsa_circ_112764,RMVar_hsa_circ_120726,RMVar_hsa_circ_238058,RMVar_hsa_circ_238059,RMVar_hsa_circ_238061,RMVar_hsa_circ_238063,RMVar_hsa_circ_84161,RMVar_hsa_circ_238064,RMVar_hsa_circ_48317,RMVar_hsa_circ_106611,RMVar_hsa_circ_238065,RMVar_hsa_circ_238066 75866 RMVar_ID_75866 Human_SNP_ID_272979003 m1A Human chr6 + 35470264 35470264 35470264 CGAATCCTCGGCCCAGGTTTAAATAAGGCAGGAAAGTTCCCTTCCCTGCTCACACACAACGAAAA CGAATCCTCGGCCCAGGTTTAAATAAGGCAGGGAAGTTCCCTTCCCTGCTCACACACAACGAAAA A G RPL10A Ensembl:ENSG00000198755 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:35470214..35470355 26863196 MeRIP-seq:(Medium) rs759383989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663335,Human_RBP_ID_1395359,Human_RBP_ID_7598568,Human_RBP_ID_9193955,Human_RBP_ID_17306929,Human_RBP_ID_17421657,Human_RBP_ID_24160035 Human_Splice_Rec_764550,Human_Splice_Rec_764551,Human_Splice_Rec_764558,Human_Splice_Rec_764559,Human_Splice_Rec_764566,Human_Splice_Rec_764567,Human_Splice_Rec_764574,Human_Splice_Rec_764575,Human_Splice_Rec_764584,Human_Splice_Rec_764585 RMVar_hsa_circ_96266,RMVar_hsa_circ_88658,RMVar_hsa_circ_115289,RMVar_hsa_circ_112764,RMVar_hsa_circ_120726,RMVar_hsa_circ_238058,RMVar_hsa_circ_238059,RMVar_hsa_circ_238061,RMVar_hsa_circ_238063,RMVar_hsa_circ_84161,RMVar_hsa_circ_238064,RMVar_hsa_circ_48317,RMVar_hsa_circ_106611,RMVar_hsa_circ_238065,RMVar_hsa_circ_238066 75867 RMVar_ID_75867 Human_SNP_ID_272979139 m1A Human chr6 + 35470623 35470623 35470623 GGCTGTAGCTGTTGGTCACGTGAAGATGACAGACGATGAGCTTGTGTATAACATTCACCTGGCTG GGCTGTAGCTGTTGGTCACGTGAAGATGACAGCCGATGAGCTTGTGTATAACATTCACCTGGCTG A C RPL10A Ensembl:ENSG00000198755 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35470576..35470675 32194978 MeRIP-seq:(Medium) rs770290088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663338,Human_RBP_ID_1672436,Human_RBP_ID_2019859,Human_RBP_ID_8643895,Human_RBP_ID_9193956,Human_RBP_ID_17308875,Human_RBP_ID_17421660,Human_RBP_ID_18085334,Human_RBP_ID_23214802,Human_RBP_ID_24160038,Human_RBP_ID_27097411,Human_RBP_ID_27346587 Human_Splice_Rec_764552,Human_Splice_Rec_764560,Human_Splice_Rec_764568,Human_Splice_Rec_764576,Human_Splice_Rec_764586 RMVar_hsa_circ_96266,RMVar_hsa_circ_115289,RMVar_hsa_circ_120726,RMVar_hsa_circ_238059,RMVar_hsa_circ_238061,RMVar_hsa_circ_84161,RMVar_hsa_circ_238064,RMVar_hsa_circ_106611,RMVar_hsa_circ_238065,RMVar_hsa_circ_115258,RMVar_hsa_circ_238066,RMVar_hsa_circ_238067 75868 RMVar_ID_75868 Human_SNP_ID_272979166 m1A Human chr6 + 35470716 35470716 35470716 AAACTGGCAGAATGTCCGGGCCTTATATATCAAGAGCACCATGGGCAAGCCCCAGCGCCTATATT AAACTGGCAGAATGTCCGGGCCTTATATATCAGGAGCACCATGGGCAAGCCCCAGCGCCTATATT A G RPL10A Ensembl:ENSG00000198755 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35470701..35470775 32194978 MeRIP-seq:(Medium) rs1185767869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17663724,Human_RBP_ID_24554547,Human_RBP_ID_26046834,Human_RBP_ID_26828461 RMVar_hsa_circ_96266,RMVar_hsa_circ_115289,RMVar_hsa_circ_120726,RMVar_hsa_circ_238059,RMVar_hsa_circ_238061,RMVar_hsa_circ_84161,RMVar_hsa_circ_238064,RMVar_hsa_circ_106611,RMVar_hsa_circ_238065,RMVar_hsa_circ_115258,RMVar_hsa_circ_238066,RMVar_hsa_circ_238067 75869 RMVar_ID_75869 Human_SNP_ID_272980234 m1A Human chr6 + 35474230 35474228 35474231 TCTTCCTGGGGCCCCTGGCTGGCTTGTGGGCTAATGAGGTGCTAATGGGGTCTAGTAGCTGCTGT TCTTCCTGGGGCCCCTGGCTGGCTTGTGGGC___TGAGGTGCTAATGGGGTCTAGTAGCTGCTGT CTAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35474180..35474328 26863196 MeRIP-seq:(Medium) rs145631362 Functional Loss DEL dbSNP153 32..34 33 - - - 75870 RMVar_ID_75870 Human_SNP_ID_272980236 m1A Human chr6 + 35474230 35474230 35474230 TCTTCCTGGGGCCCCTGGCTGGCTTGTGGGCTAATGAGGTGCTAATGGGGTCTAGTAGCTGCTGT TCTTCCTGGGGCCCCTGGCTGGCTTGTGGGCTCATGAGGTGCTAATGGGGTCTAGTAGCTGCTGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35474180..35474328 26863196 MeRIP-seq:(Medium) rs1269487524 Functional Loss SNV dbSNP153 33..33 33 - - - 75871 RMVar_ID_75871 Human_SNP_ID_272980346 m1A Human chr6 - 35474667 35474667 35474667 TTGGGGGAGCATGATGGGCAGGTGAGGGCAGGATGGAGACCAAGGGAGTCAGTGAGCAGAGGCCC TTGGGGGAGCATGATGGGCAGGTGAGGGCAGGCTGGAGACCAAGGGAGTCAGTGAGCAGAGGCCC T G TEAD3 Ensembl:ENSG00000007866 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35474558..35474804 26863196 MeRIP-seq:(Medium) rs1318546078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8237597,Human_RBP_ID_18171456,Human_RBP_ID_26539313 Human_miRNA_ID_266641 75872 RMVar_ID_75872 Human_SNP_ID_272980665 m1A Human chr6 - 35475671 35475671 35475671 GACCTCAACAGCACCATCCAGGAGGGCCCGGGAGCCTTCTATGGGGTCAGCTCTCAGTACAGCTC GACCTCAACAGCACCATCCAGGAGGGCCCGGGGGCCTTCTATGGGGTCAGCTCTCAGTACAGCTC T C TEAD3 Ensembl:ENSG00000007866 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35475626..35475675 32194978 MeRIP-seq:(Medium) rs992013336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_764602,Human_Splice_Rec_764626,Human_Splice_Rec_764650 RMVar_hsa_circ_15852,RMVar_hsa_circ_8780 75873 RMVar_ID_75873 Human_SNP_ID_272983358 m1A Human chr6 - 35486590 35486590 35486590 AGGCCCGGGAGGATGGGCCCGAGGGCCTGGACAAGGGGCTGGACAACGATGCGGAGGGCGTGTGG AGGCCCGGGAGGATGGGCCCGAGGGCCTGGACGAGGGGCTGGACAACGATGCGGAGGGCGTGTGG T C TEAD3 Ensembl:ENSG00000007866 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:35486540..35486690 26863196 MeRIP-seq:(Medium) rs749744053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2972957,Human_miRNA_ID_3006141 RMVar_hsa_circ_125422,RMVar_hsa_circ_85049,RMVar_hsa_circ_238068,RMVar_hsa_circ_238069 75874 RMVar_ID_75874 Human_SNP_ID_273005962 m1A Human chr6 - 35577028 35577028 35577028 GCACAACGAGCGGGACCGCAGGATATACGCCAACATGTTCAAGAAGTTTGCAGAGCAGGATGCCA GCACAACGAGCGGGACCGCAGGATATACGCCAGCATGTTCAAGAAGTTTGCAGAGCAGGATGCCA T C FKBP5 Ensembl:ENSG00000096060 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35575829..35577031 32194978 MeRIP-seq:(Medium) rs747710519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437,Human_RBP_ID_7598640,Human_RBP_ID_26353868 Human_Splice_Rec_764797,Human_Splice_Rec_764817,Human_Splice_Rec_764835 RMVar_hsa_circ_350550,RMVar_hsa_circ_361578 75875 RMVar_ID_75875 Human_SNP_ID_273068703 m1A Human chr6 - 35833962 35833962 35833962 ACTTGACCTAGAATATTACATATTCCTCCAGTAAGTAATACTGAAGAGCAAAAGAGAGGCAGGAT ACTTGACCTAGAATATTACATATTCCTCCAGTCAGTAATACTGAAGAGCAAAAGAGAGGCAGGAT T G SRPK1 Ensembl:ENSG00000096063 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35833664..35833965 32194978 MeRIP-seq:(Medium) rs1187912042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663426,Human_RBP_ID_8215642,Human_RBP_ID_15805478,Human_RBP_ID_17535987,Human_RBP_ID_26541175 RMVar_hsa_circ_103457,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238085,RMVar_hsa_circ_78882,RMVar_hsa_circ_103015,RMVar_hsa_circ_238087,RMVar_hsa_circ_238088,RMVar_hsa_circ_238086,RMVar_hsa_circ_238084 75876 RMVar_ID_75876 Human_SNP_ID_273069018 m1A Human chr6 - 35835375 35835375 35835375 AGGCAGCTGGCTTCACAGATTTCTTACTGCCCATGTTGGAGCTGATCCCTGAGAAGAGAGCCACT AGGCAGCTGGCTTCACAGATTTCTTACTGCCCGTGTTGGAGCTGATCCCTGAGAAGAGAGCCACT T C SRPK1 Ensembl:ENSG00000096063 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35835326..35835400 32194978 MeRIP-seq:(Medium) rs1375768451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79105,Human_RBP_ID_663453,Human_RBP_ID_1672466,Human_RBP_ID_4887074,Human_RBP_ID_7598918,Human_RBP_ID_8643945,Human_RBP_ID_15805588,Human_RBP_ID_18075299,Human_RBP_ID_18864577,Human_RBP_ID_26353180 RMVar_hsa_circ_103457,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238085,RMVar_hsa_circ_78882,RMVar_hsa_circ_103015,RMVar_hsa_circ_238087,RMVar_hsa_circ_238088,RMVar_hsa_circ_238086,RMVar_hsa_circ_238084 75877 RMVar_ID_75877 Human_SNP_ID_273077254 m1A Human chr6 + 35870397 35870397 35870397 GTCTTTTTTGCCCAGGGCCCGACTCTTTCTCCATTTCCTCAATTTCCTGCATTCGCTTCTCTAGT GTCTTTTTTGCCCAGGGCCCGACTCTTTCTCCGTTTCCTCAATTTCCTGCATTCGCTTCTCTAGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:35870346..35870448 26863196 MeRIP-seq:(Medium) rs1012306050 Functional Loss SNV dbSNP153 33..33 33 - - - 75878 RMVar_ID_75878 Human_SNP_ID_273077764 m1A Human chr6 + 35872576 35872576 35872576 TCCCTAAAAGAAAATACACCTGCAGATCCGGAAGGCGGAGGAGCTCCAGATCGCTGCCATTCTGT TCCCTAAAAGAAAATACACCTGCAGATCCGGACGGCGGAGGAGCTCCAGATCGCTGCCATTCTGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:35870342..35874258 32194978 MeRIP-seq:(Medium) rs1406817542 Functional Loss SNV dbSNP153 33..33 33 - - - 75879 RMVar_ID_75879 Human_SNP_ID_273114856 m1A Human chr6 + 36027852 36027852 36027852 GCGGGCGCAGCAGCTGGAACGGGAGTACTGCGACGCAGCCCGGAGTCGGCCTTGTAGGGGCGAAG GCGGGCGCAGCAGCTGGAACGGGAGTACTGCGTCGCAGCCCGGAGTCGGCCTTGTAGGGGCGAAG A T MAPK14 Ensembl:ENSG00000112062 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36027803..36028082 26863196 MeRIP-seq:(Medium) rs1416904741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663498,Human_RBP_ID_4903983,Human_RBP_ID_7599725,Human_RBP_ID_18425423,Human_RBP_ID_18864700,Human_RBP_ID_23067717 Human_Splice_Rec_765383 75880 RMVar_ID_75880 Human_SNP_ID_273114864 m1A Human chr6 - 36027872 36027872 36027872 CCGCCGCGATCTCCCTGCACCTTCGCCCCTACAAGGCCGACTCCGGGCTGCGTCGCAGTACTCCC CCGCCGCGATCTCCCTGCACCTTCGCCCCTACGAGGCCGACTCCGGGCTGCGTCGCAGTACTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:36027821..36027901 26863196 MeRIP-seq:(Medium) rs185564627 Functional Loss SNV dbSNP153 33..33 33 - - - 75881 RMVar_ID_75881 Human_SNP_ID_273120238 m1A Human chr6 + 36050866 36050866 36050866 CTAGAAATGGCCTAGTTTCAGAGATGGAGGGGAGGTTCAGAAAAGAGGTTGAAGATTTATAGGAG CTAGAAATGGCCTAGTTTCAGAGATGGAGGGGCGGTTCAGAAAAGAGGTTGAAGATTTATAGGAG A C MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:36050863..36050956 26863196 MeRIP-seq:(Medium) rs927613860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21604,RMVar_hsa_circ_61855 75882 RMVar_ID_75882 Human_SNP_ID_273124010 m1A Human chr6 + 36068031 36068028 36068032 ACAATAATGCTATAACTAAAAAGAAAAGGTAGAAAGGTAGAACAGGAAAGGGGAATTAGGAGTAC ACAATAATGCTATAACTAAAAAGAAAAGGT____AGGTAGAACAGGAAAGGGGAATTAGGAGTAC TAGAA T MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36068029..36068310 26863196 MeRIP-seq:(Medium) rs377367391 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_7599843 RMVar_hsa_circ_19317,RMVar_hsa_circ_21604,RMVar_hsa_circ_61855,RMVar_hsa_circ_119395,RMVar_hsa_circ_294495,RMVar_hsa_circ_67377,RMVar_hsa_circ_238115,RMVar_hsa_circ_266981 75883 RMVar_ID_75883 Human_SNP_ID_273128759 m1A Human chr6 + 36089347 36089347 36089347 GTGGGAGCTGAACAATGAGAACACATGGACACATGGAGGAGAACAACACACGCTGGGGCCTGTTG GTGGGAGCTGAACAATGAGAACACATGGACACCTGGAGGAGAACAACACACGCTGGGGCCTGTTG A C MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36089344..36089435 26863196 MeRIP-seq:(Medium) rs1299166765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6492,RMVar_hsa_circ_19317,RMVar_hsa_circ_67377,RMVar_hsa_circ_266981,RMVar_hsa_circ_275682,RMVar_hsa_circ_62121,RMVar_hsa_circ_30071,RMVar_hsa_circ_238118,RMVar_hsa_circ_238120 75884 RMVar_ID_75884 Human_SNP_ID_273155265 m1A Human chr6 - 36201112 36201112 36201112 ATTGGGGCAAAGGATGCAATCCACAGGCCGGGAGGGAGACTGCAGGCAGCAGCGGCATAGCCACT ATTGGGGCAAAGGATGCAATCCACAGGCCGGGTGGGAGACTGCAGGCAGCAGCGGCATAGCCACT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:36200888..36201138 32194978 MeRIP-seq:(Medium) rs760376981 Functional Loss SNV dbSNP153 33..33 33 - - - 75885 RMVar_ID_75885 Human_SNP_ID_273224016 m1A Human chr6 + 36481727 36481727 36481727 GGATGAGGATTCTGTGGACTGGGATGAAGACCACCCTCCACCAATGGGGGAGGAATATTCCCAAA GGATGAGGATTCTGTGGACTGGGATGAAGACCGCCCTCCACCAATGGGGGAGGAATATTCCCAAA A G KCTD20 Ensembl:ENSG00000112078 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36474964..36484793 32194978 MeRIP-seq:(Medium) rs370414424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949518,Human_RBP_ID_8644237,Human_RBP_ID_9400487,Human_RBP_ID_18075510 Human_Splice_Rec_765917,Human_Splice_Rec_765931,Human_Splice_Rec_765951,Human_Splice_Rec_765961,Human_Splice_Rec_765969,Human_Splice_Rec_765981 RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 75886 RMVar_ID_75886 Human_SNP_ID_273224017 m1A Human chr6 + 36481727 36481727 36481727 GGATGAGGATTCTGTGGACTGGGATGAAGACCACCCTCCACCAATGGGGGAGGAATATTCCCAAA GGATGAGGATTCTGTGGACTGGGATGAAGACCTCCCTCCACCAATGGGGGAGGAATATTCCCAAA A T KCTD20 Ensembl:ENSG00000112078 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36474964..36484793 32194978 MeRIP-seq:(Medium) rs370414424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949518,Human_RBP_ID_8644237,Human_RBP_ID_9400487,Human_RBP_ID_18075510 Human_Splice_Rec_765917,Human_Splice_Rec_765931,Human_Splice_Rec_765951,Human_Splice_Rec_765961,Human_Splice_Rec_765969,Human_Splice_Rec_765981 RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 75887 RMVar_ID_75887 Human_SNP_ID_273226135 m1A Human chr6 - 36490002 36490002 36490002 TTTAAAGTAGTACTGGGTACTGCATATTGTGCAGTAAATCTGGCTTGCTTTCTTAACCTTTTTGC TTTAAAGTAGTACTGGGTACTGCATATTGTGCCGTAAATCTGGCTTGCTTTCTTAACCTTTTTGC T G RF00017-4630,RF00017-4489 RNACentral:URS000096585E,RNACentral:URS00009982F9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:36489952..36490041 26863196 MeRIP-seq:(Medium) rs1018818845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238129 75888 RMVar_ID_75888 Human_SNP_ID_273227310 m1A Human chr6 + 36494910 36494910 36494910 GCCTAGGCCTGGGCTCTCCTCGTTAGGTTCCCAGGAATAAATTGAGTTCCCATTGGCAGCACTTG GCCTAGGCCTGGGCTCTCCTCGTTAGGTTCCCCGGAATAAATTGAGTTCCCATTGGCAGCACTTG A C RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36494751..36494975 32194978 MeRIP-seq:(Medium) rs1466481744 Functional Loss SNV dbSNP153 33..33 33 - - - 75889 RMVar_ID_75889 Human_SNP_ID_273240737 m1A Human chr6 + 36547337 36547336 36547337 GACGGGAGGGGACGCGTGAGGGACTCTGAGACAGGGGGCAACAGGCGGTTACGGGTGAGGACAAC GACGGGAGGGGACGCGTGAGGGACTCTGAGAC_GGGGGCAACAGGCGGTTACGGGTGAGGACAAC CA C RF00017-5484,RF00017-4674 RNACentral:URS00009A6CA9,RNACentral:URS000094E2D9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:36547289..36547428 26863196 MeRIP-seq:(Medium) rs1225005702 Functional Loss DEL dbSNP153 33..33 33 - - - 75890 RMVar_ID_75890 Human_SNP_ID_273249247 m1A Human chr6 + 36579868 36579868 36579868 TAAACTTACTTCCCTGTATTTGTGAGTTCCAGAGTGCAAGCTAGGGTCACCGAAACAAAGGTTTC TAAACTTACTTCCCTGTATTTGTGAGTTCCAGGGTGCAAGCTAGGGTCACCGAAACAAAGGTTTC A G RF00017-5484,RF00017-4674 RNACentral:URS00009A6CA9,RNACentral:URS000094E2D9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36579743..36579929 26863196 MeRIP-seq:(Medium) rs1227157890 Functional Loss SNV dbSNP153 33..33 33 - - - 75891 RMVar_ID_75891 Human_SNP_ID_273253333 m1A Human chr6 + 36594427 36594427 36594427 GTTGGTTGGTGTTGGGCCGGAGGAAAGCGGGAAGACTCATCGGAGCGTGTGGATTTGAGCCGCCG GTTGGTTGGTGTTGGGCCGGAGGAAAGCGGGACGACTCATCGGAGCGTGTGGATTTGAGCCGCCG A C SRSF3 Ensembl:ENSG00000112081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr6:36594351..36594536;chr6:36594376..36594450;chr6:36594376..36594548;chr6:36594376..36594500;chr6:36594376..36594529;chr6:36594351..36594532;chr6:36594351..36594612;chr6:36594351..36594544;chr6:36594376..36594551 26863196 MeRIP-seq:(Medium) rs1048397585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663630,Human_RBP_ID_789471,Human_RBP_ID_842166,Human_RBP_ID_1069742,Human_RBP_ID_1217691,Human_RBP_ID_1672667,Human_RBP_ID_2020365,Human_RBP_ID_3808256,Human_RBP_ID_4887671,Human_RBP_ID_5122477,Human_RBP_ID_5451210,Human_RBP_ID_7600759,Human_RBP_ID_9336649,Human_RBP_ID_9400491,Human_RBP_ID_15811689,Human_RBP_ID_18075561,Human_RBP_ID_18864898,Human_RBP_ID_19129221,Human_RBP_ID_22105044,Human_RBP_ID_23067827,Human_RBP_ID_23138966,Human_RBP_ID_24160830,Human_RBP_ID_24548570,Human_RBP_ID_26353183,Human_RBP_ID_27097656 Human_Splice_Rec_766019,Human_Splice_Rec_766025,Human_Splice_Rec_766035,Human_Splice_Rec_766037,Human_Splice_Rec_766043 Human_miRNA_ID_2947076 RMVar_hsa_circ_99475,RMVar_hsa_circ_238149 75892 RMVar_ID_75892 Human_SNP_ID_273253340 m1A Human chr6 + 36594461 36594461 36594461 ACTCATCGGAGCGTGTGGATTTGAGCCGCCGCATTTTTTAACCCTAGATCTCGGTAAGAGACCAG ACTCATCGGAGCGTGTGGATTTGAGCCGCCGCCTTTTTTAACCCTAGATCTCGGTAAGAGACCAG A C SRSF3 Ensembl:ENSG00000112081 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:36594351..36594525 26863410 MeRIP-seq:(Medium) rs1014175480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663634,Human_RBP_ID_947617,Human_RBP_ID_1047371,Human_RBP_ID_1069742,Human_RBP_ID_1672667,Human_RBP_ID_2020365,Human_RBP_ID_3006001,Human_RBP_ID_4887671,Human_RBP_ID_7600759,Human_RBP_ID_9336649,Human_RBP_ID_9400492,Human_RBP_ID_15811690,Human_RBP_ID_18075561,Human_RBP_ID_18170974,Human_RBP_ID_18450359,Human_RBP_ID_19016950,Human_RBP_ID_19129221,Human_RBP_ID_22105045,Human_RBP_ID_22514237,Human_RBP_ID_23067827,Human_RBP_ID_24160830,Human_RBP_ID_24548570,Human_RBP_ID_26353186,Human_RBP_ID_27097656,Human_RBP_ID_27827621 Human_Splice_Rec_766019,Human_Splice_Rec_766025,Human_Splice_Rec_766035,Human_Splice_Rec_766037,Human_Splice_Rec_766043 RMVar_hsa_circ_99475,RMVar_hsa_circ_238149 75893 RMVar_ID_75893 Human_SNP_ID_273253342 m1A Human chr6 + 36594469 36594469 36594469 GAGCGTGTGGATTTGAGCCGCCGCATTTTTTAACCCTAGATCTCGGTAAGAGACCAGCGAAAGAG GAGCGTGTGGATTTGAGCCGCCGCATTTTTTAGCCCTAGATCTCGGTAAGAGACCAGCGAAAGAG A G SRSF3 Ensembl:ENSG00000112081 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:36594386..36594486 26863410 MeRIP-seq:(Medium) rs1246815561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663635,Human_RBP_ID_947617,Human_RBP_ID_1047371,Human_RBP_ID_1069742,Human_RBP_ID_1672667,Human_RBP_ID_2020365,Human_RBP_ID_3006001,Human_RBP_ID_4905465,Human_RBP_ID_9336649,Human_RBP_ID_9400493,Human_RBP_ID_15811691,Human_RBP_ID_18075561,Human_RBP_ID_18170974,Human_RBP_ID_18450359,Human_RBP_ID_19016950,Human_RBP_ID_19129221,Human_RBP_ID_22105045,Human_RBP_ID_22312431,Human_RBP_ID_23061575,Human_RBP_ID_24160830,Human_RBP_ID_24548570,Human_RBP_ID_26003555,Human_RBP_ID_26353186,Human_RBP_ID_27827621 Human_Splice_Rec_766019,Human_Splice_Rec_766025,Human_Splice_Rec_766035,Human_Splice_Rec_766037,Human_Splice_Rec_766043 RMVar_hsa_circ_99475,RMVar_hsa_circ_238149 75894 RMVar_ID_75894 Human_SNP_ID_273254282 m1A Human chr6 - 36596693 36596692 36596694 AAACATCTACAGTTAAAACCACAGATCCTTAGAAAGAACTCCATTAGAGAGGACAAGAGAGTTTA AAACATCTACAGTTAAAACCACAGATCCTTA__AAGAACTCCATTAGAGAGGACAAGAGAGTTTA TTC T RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:36596690..36596850 26863410 MeRIP-seq:(Medium) rs536285602 Functional Loss DEL dbSNP153 32..33 33 - - - 75895 RMVar_ID_75895 Human_SNP_ID_273254283 m1A Human chr6 - 36596693 36596693 36596693 AAACATCTACAGTTAAAACCACAGATCCTTAGAAAGAACTCCATTAGAGAGGACAAGAGAGTTTA AAACATCTACAGTTAAAACCACAGATCCTTAGGAAGAACTCCATTAGAGAGGACAAGAGAGTTTA T C RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:36596690..36596850 26863410 MeRIP-seq:(Medium) rs60049609 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9184 75896 RMVar_ID_75896 Human_SNP_ID_273254324 m1A Human chr6 + 36596837 36596837 36596837 GGCAATCTTGGAAACAATGGCAACAAGACGGAATTGGAACGGGCTTTTGGCTACTATGGACCACT GGCAATCTTGGAAACAATGGCAACAAGACGGAGTTGGAACGGGCTTTTGGCTACTATGGACCACT A G SRSF3 Ensembl:ENSG00000112081 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:36594711..36597017;chr6:36596751..36597003;chr6:36596751..36597028 26863196 MeRIP-seq:(Medium) rs1179651719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663637,Human_RBP_ID_1672671,Human_RBP_ID_2020371,Human_RBP_ID_3808265,Human_RBP_ID_4913328,Human_RBP_ID_5219188,Human_RBP_ID_5617909,Human_RBP_ID_7600811,Human_RBP_ID_8644305,Human_RBP_ID_8901201,Human_RBP_ID_9400496,Human_RBP_ID_15811831,Human_RBP_ID_17536049,Human_RBP_ID_18075562,Human_RBP_ID_18864902,Human_RBP_ID_22772743,Human_RBP_ID_24160836,Human_RBP_ID_26353187 Human_Splice_Rec_766020,Human_Splice_Rec_766026,Human_Splice_Rec_766036,Human_Splice_Rec_766038,Human_Splice_Rec_766044,Human_Splice_Rec_766056 Human_miRNA_ID_2667848 RMVar_hsa_circ_99475,RMVar_hsa_circ_94942,RMVar_hsa_circ_238149,RMVar_hsa_circ_238150 75897 RMVar_ID_75897 Human_SNP_ID_273255100 m1A Human chr6 - 36599011 36599011 36599011 CCTGCTCCTACTAGCTACTCCATTACACCAATACCTCTTAACAAGCTTTCTCTCAAGTACCTGCG CCTGCTCCTACTAGCTACTCCATTACACCAATCCCTCTTAACAAGCTTTCTCTCAAGTACCTGCG T G RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:36599009..36599115 26863196 MeRIP-seq:(Medium) rs1303297841 Functional Loss SNV dbSNP153 33..33 33 - - - 75898 RMVar_ID_75898 Human_SNP_ID_273255348 m1A Human chr6 - 36599881 36599881 36599881 TGAATGGGGCGCGCTGGTCACATGACGCTGAAAGGGCTAGTTGACTGGCTAATGCAGATTCAGAG TGAATGGGGCGCGCTGGTCACATGACGCTGAACGGGCTAGTTGACTGGCTAATGCAGATTCAGAG T G RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36599876..36600125 32194978 MeRIP-seq:(Medium) rs1281962777 Functional Loss SNV dbSNP153 33..33 33 - - - 75899 RMVar_ID_75899 Human_SNP_ID_273265980 m1A Human chr6 + 36639599 36639599 36639599 CATTTGGGGAAATCACAGGGGTCAGCACATCCAGAGTGCAATGGATAAGCCTCGCCCTGGGAAAA CATTTGGGGAAATCACAGGGGTCAGCACATCCGGAGTGCAATGGATAAGCCTCGCCCTGGGAAAA A G RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36639576..36639650 26863196 MeRIP-seq:(Medium) rs903878394 Functional Loss SNV dbSNP153 33..33 33 - - - 75900 RMVar_ID_75900 Human_SNP_ID_273276881 m1A Human chr6 - 36684166 36684166 36684166 CGCGGCTCAGCTGCTCGCTGTCCACTGGGCCGAAGAGGCGGCGGCAGGCCTTGCTGCCGCATGGG CGCGGCTCAGCTGCTCGCTGTCCACTGGGCCGGAGAGGCGGCGGCAGGCCTTGCTGCCGCATGGG T C RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:36684067..36684381 26863196 MeRIP-seq:(Medium) rs1253386083 Functional Loss SNV dbSNP153 33..33 33 - - - 75901 RMVar_ID_75901 Human_SNP_ID_273277012 m1A Human chr6 - 36684450 36684450 36684450 AGCCTGCTCCCCTGAGCGAGGCACAAGGGTACAAGACAGTGACAGGTCCACATGGTCTTCCTCTG AGCCTGCTCCCCTGAGCGAGGCACAAGGGTACGAGACAGTGACAGGTCCACATGGTCTTCCTCTG T C RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:36684401..36684450 32194978 MeRIP-seq:(Medium) rs1430921510 Functional Loss SNV dbSNP153 33..33 33 - - - 75902 RMVar_ID_75902 Human_SNP_ID_273318881 m1A Human chr6 + 36855806 36855806 36855806 GGGGCCATCTCAGAAGAGCTGCTCAAGAGGGTAGCAAGTCTACCCAGAAGGGTATGCCTTAATGA GGGGCCATCTCAGAAGAGCTGCTCAAGAGGGTGGCAAGTCTACCCAGAAGGGTATGCCTTAATGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36855608..36855805 32194978 MeRIP-seq:(Medium) rs1036990995 Functional Loss SNV dbSNP153 33..33 33 - - - 75903 RMVar_ID_75903 Human_SNP_ID_273320896 m1A Human chr6 - 36863649 36863649 36863649 AGAATGGGGAGAAGTAGAGACACTTGGTGTTGACAGCTTTTTCAAGGAGTTTTTCTGTGAAGGGA AGAATGGGGAGAAGTAGAGACACTTGGTGTTGTCAGCTTTTTCAAGGAGTTTTTCTGTGAAGGGA T A PPIL1 Ensembl:ENSG00000137168 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36863647..36863776 26863196 MeRIP-seq:(Medium) rs1480020277 Functional Loss SNV dbSNP153 33..33 33 - - - 75904 RMVar_ID_75904 Human_SNP_ID_273323396 m1A Human chr6 - 36874763 36874763 36874763 AGCATTCCGCCGCCGGCTTCGCTATGGCGGCAATTCCCCCAGATTCCTGGCAGCCACCCAACGTT AGCATTCCGCCGCCGGCTTCGCTATGGCGGCAGTTCCCCCAGATTCCTGGCAGCCACCCAACGTT T C PPIL1 Ensembl:ENSG00000137168 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:36874697..36874771 26863196 MeRIP-seq:(Medium) rs755549469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285126,Human_RBP_ID_663769,Human_RBP_ID_1047423,Human_RBP_ID_4887890,Human_RBP_ID_5428527,Human_RBP_ID_18075680,Human_RBP_ID_18425911 Human_Splice_Rec_766289 75905 RMVar_ID_75905 Human_SNP_ID_273325984 m1A Human chr6 + 36886027 36886027 36886027 GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCATGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCCTGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG A C C6orf89 Ensembl:ENSG00000198663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36886006..36886085 26863196 MeRIP-seq:(Medium) rs759883998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903307,Human_RBP_ID_17421663,Human_RBP_ID_19129228 Human_Splice_Rec_766313,Human_Splice_Rec_766329,Human_Splice_Rec_766343 75906 RMVar_ID_75906 Human_SNP_ID_273325985 m1A Human chr6 + 36886027 36886027 36886027 GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCATGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCGTGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG A G C6orf89 Ensembl:ENSG00000198663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36886006..36886085 26863196 MeRIP-seq:(Medium) rs759883998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903307,Human_RBP_ID_17421663,Human_RBP_ID_19129228 Human_Splice_Rec_766313,Human_Splice_Rec_766329,Human_Splice_Rec_766343 75907 RMVar_ID_75907 Human_SNP_ID_273325986 m1A Human chr6 + 36886027 36886027 36886027 GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCATGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG GGCGGGAGGAGCCCGAGGGGCGCGAGCCCCGCTTGTGAGTGACTGGGGCCCGAGGCTGGGTGGGG A T C6orf89 Ensembl:ENSG00000198663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36886006..36886085 26863196 MeRIP-seq:(Medium) rs759883998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903307,Human_RBP_ID_17421663,Human_RBP_ID_19129228 Human_Splice_Rec_766313,Human_Splice_Rec_766329,Human_Splice_Rec_766343 75908 RMVar_ID_75908 Human_SNP_ID_273346894 m1A Human chr6 - 36968838 36968838 36968838 GGCCACCGTGGGTGAGGCCTGACCACCTTGGGACACCTGCAAGACGACTCCAACCCAACAACAAC GGCCACCGTGGGTGAGGCCTGACCACCTTGGGTCACCTGCAAGACGACTCCAACCCAACAACAAC T A MTCH1 Ensembl:ENSG00000137409 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36968790..36968975 26863196 MeRIP-seq:(Medium) rs1485616750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663890,Human_RBP_ID_1672901,Human_RBP_ID_2020513,Human_RBP_ID_17307063,Human_RBP_ID_17421674,Human_RBP_ID_18450367,Human_RBP_ID_18539104,Human_RBP_ID_18865047,Human_RBP_ID_22105072,Human_RBP_ID_23067828,Human_RBP_ID_26536413 Human_miRNA_ID_2610974 RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_117941,RMVar_hsa_circ_94387,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_238169,RMVar_hsa_circ_87795,RMVar_hsa_circ_238170,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164 75909 RMVar_ID_75909 Human_SNP_ID_273346895 m1A Human chr6 - 36968838 36968838 36968838 GGCCACCGTGGGTGAGGCCTGACCACCTTGGGACACCTGCAAGACGACTCCAACCCAACAACAAC GGCCACCGTGGGTGAGGCCTGACCACCTTGGGGCACCTGCAAGACGACTCCAACCCAACAACAAC T C MTCH1 Ensembl:ENSG00000137409 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36968790..36968975 26863196 MeRIP-seq:(Medium) rs1485616750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663890,Human_RBP_ID_1672901,Human_RBP_ID_2020513,Human_RBP_ID_17307063,Human_RBP_ID_17421674,Human_RBP_ID_18450367,Human_RBP_ID_18539104,Human_RBP_ID_18865047,Human_RBP_ID_22105072,Human_RBP_ID_23067828,Human_RBP_ID_26536413 Human_miRNA_ID_2610974 RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_117941,RMVar_hsa_circ_94387,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_238169,RMVar_hsa_circ_87795,RMVar_hsa_circ_238170,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164 75910 RMVar_ID_75910 Human_SNP_ID_273346898 m1A Human chr6 + 36968843 36968843 36968843 TGTTGGGTTGGAGTCGTCTTGCAGGTGTCCCAAGGTGGTCAGGCCTCACCCACGGTGGCCAGGTT TGTTGGGTTGGAGTCGTCTTGCAGGTGTCCCAGGGTGGTCAGGCCTCACCCACGGTGGCCAGGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:36968504..36968981 26863196 MeRIP-seq:(Medium) rs1487462180 Functional Loss SNV dbSNP153 33..33 33 - - - 75911 RMVar_ID_75911 Human_SNP_ID_273349191 m1A Human chr6 - 36977837 36977837 36977837 AGCACTCCTGGGTGGGGGACTGGGGAGTGGGCAACAGGTGGAGCCATCCTTGGCAGACCGACCCC AGCACTCCTGGGTGGGGGACTGGGGAGTGGGCCACAGGTGGAGCCATCCTTGGCAGACCGACCCC T G MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36977836..36978095 26863196 MeRIP-seq:(Medium) rs1561908684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5398810,Human_RBP_ID_21990798,Human_RBP_ID_22746479,Human_RBP_ID_24562786,Human_RBP_ID_27842454 RMVar_hsa_circ_23450,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238165,RMVar_hsa_circ_238164 75912 RMVar_ID_75912 Human_SNP_ID_273349381 m1A Human chr6 + 36978527 36978527 36978527 GTGGGCTCACCTTCTTCATGCTACCCCGAGTCACAGTAGAGAGGGCGTTGGACATCAGCCGGGGA GTGGGCTCACCTTCTTCATGCTACCCCGAGTCGCAGTAGAGAGGGCGTTGGACATCAGCCGGGGA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36978501..36978600 26863196 MeRIP-seq:(Medium) rs951989042 Functional Loss SNV dbSNP153 33..33 33 - - - 75913 RMVar_ID_75913 Human_SNP_ID_273350164 m1A Human chr6 + 36981617 36981617 36981617 CACCGTAGGTGAAGAAGCTCGGCAGATAGAGGACCTTCCTCCCCAGCACATTGGTCCCAAGGGTG CACCGTAGGTGAAGAAGCTCGGCAGATAGAGGGCCTTCCTCCCCAGCACATTGGTCCCAAGGGTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36981601..36981625 26863196 MeRIP-seq:(Medium) rs1410145917 Functional Loss SNV dbSNP153 33..33 33 - - - 75914 RMVar_ID_75914 Human_SNP_ID_273350173 m1A Human chr6 - 36981648 36981648 36981648 TTCTGAAGGTGGGTCATGAGCCGATGCCCCCCACCCTTGGGACCAATGTGCTGGGGAGGAAGGTC TTCTGAAGGTGGGTCATGAGCCGATGCCCCCCTCCCTTGGGACCAATGTGCTGGGGAGGAAGGTC T A MTCH1 Ensembl:ENSG00000137409 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:36981626..36981650 26863196 MeRIP-seq:(Medium) rs1561911231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663902,Human_RBP_ID_952085,Human_RBP_ID_4903998 Human_Splice_Rec_766398,Human_Splice_Rec_766399,Human_Splice_Rec_766420,Human_Splice_Rec_766421,Human_Splice_Rec_766464,Human_Splice_Rec_766465 Human_miRNA_ID_2033911,Human_miRNA_ID_2035215 RMVar_hsa_circ_87795,RMVar_hsa_circ_238164,RMVar_hsa_circ_120829,RMVar_hsa_circ_35193,RMVar_hsa_circ_238173 75915 RMVar_ID_75915 Human_SNP_ID_273351175 m1A Human chr6 - 36985945 36985945 36985945 ATGGCGGGTCAGGGGGCCTGGGGTCTGGGGACAACGCCCCGACCACTGAGGCTCTTTTCGTGGCA ATGGCGGGTCAGGGGGCCTGGGGTCTGGGGACGACGCCCCGACCACTGAGGCTCTTTTCGTGGCA T C MTCH1 Ensembl:ENSG00000137409 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36985926..36985950 26863196 MeRIP-seq:(Medium) rs1325352365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663905,Human_RBP_ID_4903308,Human_RBP_ID_22618364 Human_Splice_Rec_766397,Human_Splice_Rec_766419,Human_Splice_Rec_766463 RMVar_hsa_circ_112664,RMVar_hsa_circ_238174 75916 RMVar_ID_75916 Human_SNP_ID_273351214 m1A Human chr6 - 36986045 36986045 36986045 GCGGCGGGGGTCGAGGCTCGAGCTCGCGATCCACCGCCCGCGCACCGCGCACATCCTCGCCACCC GCGGCGGGGGTCGAGGCTCGAGCTCGCGATCCGCCGCCCGCGCACCGCGCACATCCTCGCCACCC T C MTCH1 Ensembl:ENSG00000137409 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:36981651..36986150 26863410 MeRIP-seq:(Medium) rs1287137475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663906,Human_RBP_ID_4888150,Human_RBP_ID_5242559 Human_miRNA_ID_2249975 RMVar_hsa_circ_112664,RMVar_hsa_circ_238174 75917 RMVar_ID_75917 Human_SNP_ID_273387580 m1A Human chr6 + 37125926 37125926 37125926 CCAAATTGTCCTTGCCTGCCGTCCGTCTCCACACCACCCGACCTCCCTTCCCCCGCCACTTGCCC CCAAATTGTCCTTGCCTGCCGTCCGTCTCCACCCCACCCGACCTCCCTTCCCCCGCCACTTGCCC A C RF00017-4498,RF00017-4484 RNACentral:URS0000923951,RNACentral:URS00009439B4 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:37125875..37126022;chr6:37125885..37126014 26863196 MeRIP-seq:(Medium) rs910334545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5216343,Human_RBP_ID_15814642,Human_RBP_ID_26715315 75918 RMVar_ID_75918 Human_SNP_ID_273387581 m1A Human chr6 + 37125926 37125926 37125926 CCAAATTGTCCTTGCCTGCCGTCCGTCTCCACACCACCCGACCTCCCTTCCCCCGCCACTTGCCC CCAAATTGTCCTTGCCTGCCGTCCGTCTCCACGCCACCCGACCTCCCTTCCCCCGCCACTTGCCC A G RF00017-4498,RF00017-4484 RNACentral:URS0000923951,RNACentral:URS00009439B4 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:37125875..37126022;chr6:37125885..37126014 26863196 MeRIP-seq:(Medium) rs910334545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5216343,Human_RBP_ID_15814642,Human_RBP_ID_26715315 75919 RMVar_ID_75919 Human_SNP_ID_273390389 m1A Human chr6 - 37137663 37137663 37137663 AGGGGGAGCCCTGTGAAGATGAAGTTGGTTTAAGGTTAGTCGGTGATGAATAATAGCCCAAAGGC AGGGGGAGCCCTGTGAAGATGAAGTTGGTTTAGGGTTAGTCGGTGATGAATAATAGCCCAAAGGC T C lnc-TMEM217-4 RNACentral:URS0000D56D8B lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37137629..37137716 26863196 MeRIP-seq:(Medium) rs1454013439 Functional Loss SNV dbSNP153 33..33 33 - - - 75920 RMVar_ID_75920 Human_SNP_ID_273398893 m1A Human chr6 + 37170391 37170391 37170391 CGCTGGCGCGCCCTCCCGCCGCCAGTCCCGGCAGCGCCCTCAGTTGTCCTCCGACTCGCCCTCGG CGCTGGCGCGCCCTCCCGCCGCCAGTCCCGGCTGCGCCCTCAGTTGTCCTCCGACTCGCCCTCGG A T PIM1 Ensembl:ENSG00000137193 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:37170340..37170600 26863196 MeRIP-seq:(Medium) rs1343861789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904005,Human_RBP_ID_5451224,Human_RBP_ID_22534102 RMVar_hsa_circ_87286,RMVar_hsa_circ_238175 75921 RMVar_ID_75921 Human_SNP_ID_273398899 m1A Human chr6 - 37170414 37170414 37170414 GTGGCTGCGGCTGGCGCGGAAGGCCGAGGGCGAGTCGGAGGACAACTGAGGGCGCTGCCGGGACT GTGGCTGCGGCTGGCGCGGAAGGCCGAGGGCGTGTCGGAGGACAACTGAGGGCGCTGCCGGGACT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:37170228..37170501 26863410 MeRIP-seq:(Medium) rs1042528446 Functional Loss SNV dbSNP153 33..33 33 - - - 75922 RMVar_ID_75922 Human_SNP_ID_273398917 m1A Human chr6 + 37170445 37170445 37170445 CTCGCCCTCGGCCTTCCGCGCCAGCCGCAGCCACAGCCGCAACGCCACCCGCAGCCACAGCCACA CTCGCCCTCGGCCTTCCGCGCCAGCCGCAGCCCCAGCCGCAACGCCACCCGCAGCCACAGCCACA A C PIM1 Ensembl:ENSG00000137193 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:37170198..37170606 26863196 MeRIP-seq:(Medium) rs1319752632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841405,Human_RBP_ID_4904006,Human_RBP_ID_9262983,Human_RBP_ID_17421677,Human_RBP_ID_22534103 RMVar_hsa_circ_87286,RMVar_hsa_circ_238175 75923 RMVar_ID_75923 Human_SNP_ID_273398918 m1A Human chr6 + 37170445 37170445 37170445 CTCGCCCTCGGCCTTCCGCGCCAGCCGCAGCCACAGCCGCAACGCCACCCGCAGCCACAGCCACA CTCGCCCTCGGCCTTCCGCGCCAGCCGCAGCCGCAGCCGCAACGCCACCCGCAGCCACAGCCACA A G PIM1 Ensembl:ENSG00000137193 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:37170198..37170606 26863196 MeRIP-seq:(Medium) rs1319752632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_841405,Human_RBP_ID_4904006,Human_RBP_ID_9262983,Human_RBP_ID_17421677,Human_RBP_ID_22534103 RMVar_hsa_circ_87286,RMVar_hsa_circ_238175 75924 RMVar_ID_75924 Human_SNP_ID_273399390 m1A Human chr6 + 37171304 37171304 37171304 TTCGACTTCATCACGGAAAGGGGAGCCCTGCAAGAGGAGCTGGCCCGCAGCTTCTTCTGGCAGGT TTCGACTTCATCACGGAAAGGGGAGCCCTGCAGGAGGAGCTGGCCCGCAGCTTCTTCTGGCAGGT A G PIM1 Ensembl:ENSG00000137193 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37171254..37171418 26863196 MeRIP-seq:(Medium) rs370931326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790366,Human_RBP_ID_841411,Human_RBP_ID_9402063,Human_RBP_ID_17421678,Human_RBP_ID_18865071,Human_RBP_ID_22106428,Human_RBP_ID_22534106,Human_RBP_ID_22616397,Human_RBP_ID_27346917 RMVar_hsa_circ_87286,RMVar_hsa_circ_98763,RMVar_hsa_circ_104996,RMVar_hsa_circ_238175,RMVar_hsa_circ_238176,RMVar_hsa_circ_238177 75925 RMVar_ID_75925 Human_SNP_ID_273400368 m1A Human chr6 - 37174586 37174584 37174586 CCCAGGCAGATTTTTGGAGAAGCAGCAGGTAAAAGAGGCAAGTTCAAGTATTTCTCCCAGCACAG CCCAGGCAGATTTTTGGAGAAGCAGCAGGTAA__GAGGCAAGTTCAAGTATTTCTCCCAGCACAG CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37174535..37174647 26863196 MeRIP-seq:(Medium) rs1561984826 Functional Loss DEL dbSNP153 33..34 33 - - - 75926 RMVar_ID_75926 Human_SNP_ID_273420873 m1A Human chr6 - 37257831 37257831 37257831 GCCCCCAGACCCCGCAATCTGAGGGCCAACCCAGGCCGCTTCCCCGCCGCCGGTCACCCGCTCCC GCCCCCAGACCCCGCAATCTGAGGGCCAACCCGGGCCGCTTCCCCGCCGCCGGTCACCCGCTCCC T C TMEM217 Ensembl:ENSG00000172738 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:37257776..37257956;chr6:37257776..37258216;chr6:37257776..37269639;chr6:37257756..37258155 26863196 MeRIP-seq:(Medium) rs534272902 Functional Loss SNV dbSNP153 33..33 33 - - - 75927 RMVar_ID_75927 Human_SNP_ID_273444647 m1A Human chr6 - 37360453 37360453 37360453 CCAGTTGGTATGTGACACCAAATCCTCGTCCTACAGTCACCTGGGAGACAACAACAATGCAAGAA CCAGTTGGTATGTGACACCAAATCCTCGTCCTGCAGTCACCTGGGAGACAACAACAATGCAAGAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:37360426..37360475 26863196 MeRIP-seq:(Medium) rs911661753 Functional Loss SNV dbSNP153 33..33 33 - - - 75928 RMVar_ID_75928 Human_SNP_ID_273446978 m1A Human chr6 + 37370983 37370983 37370983 TGCTGGACATATAGGTTAATGATCACCTGGAAAGCTTCCACATTGGAGGGGGCTGATGAGGAAAT TGCTGGACATATAGGTTAATGATCACCTGGAACGCTTCCACATTGGAGGGGGCTGATGAGGAAAT A C RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37370978..37371123 26863196 MeRIP-seq:(Medium) rs1388276003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30464,RMVar_hsa_circ_353648,RMVar_hsa_circ_57861,RMVar_hsa_circ_275958,RMVar_hsa_circ_310293,RMVar_hsa_circ_238194,RMVar_hsa_circ_238195 75929 RMVar_ID_75929 Human_SNP_ID_273450860 m1A Human chr6 + 37388092 37388092 37388092 GGATAGGTTAGTCTGGCTGTAGTGAAGAGACGACATGGTGCTGGGAACAAGAATAAAGGCAGTAA GGATAGGTTAGTCTGGCTGTAGTGAAGAGACGGCATGGTGCTGGGAACAAGAATAAAGGCAGTAA A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:37388074..37388227 26863196 MeRIP-seq:(Medium) rs1186789831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15815523 75930 RMVar_ID_75930 Human_SNP_ID_273451363 m1A Human chr6 + 37390427 37390427 37390427 AAAGAGGGAATGGTAAGGGGGAGCATGCTGGTATGTGGGAGGGGCAGCAAGGAGGCTAGTGCTGG AAAGAGGGAATGGTAAGGGGGAGCATGCTGGTGTGTGGGAGGGGCAGCAAGGAGGCTAGTGCTGG A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37390405..37390539 26863196 MeRIP-seq:(Medium) rs1357850781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17069929,Human_RBP_ID_21990800 75931 RMVar_ID_75931 Human_SNP_ID_273451382 m1A Human chr6 + 37390507 37390507 37390507 CTGGGGAGTGGGTAGGAGAGGAAGCTTGAGCAAGACGCAGATTTTGTAGGGCCTTGTAGGCCTTT CTGGGGAGTGGGTAGGAGAGGAAGCTTGAGCAGGACGCAGATTTTGTAGGGCCTTGTAGGCCTTT A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37390384..37390715 26863196 MeRIP-seq:(Medium) rs1199072254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21990800 75932 RMVar_ID_75932 Human_SNP_ID_273461743 m1A Human chr6 - 37433287 37433287 37433287 CCGCCGCTGCCAGAGCCGCCGCCTCCTCCCTCAGTTTCGTTTCCCCACAAGCCAGCCCGGGTCCG CCGCCGCTGCCAGAGCCGCCGCCTCCTCCCTCGGTTTCGTTTCCCCACAAGCCAGCCCGGGTCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37433226..37435750 26863196 MeRIP-seq:(Medium) rs1351237489 Functional Loss SNV dbSNP153 33..33 33 - - - 75933 RMVar_ID_75933 Human_SNP_ID_273462336 m1A Human chr6 - 37435578 37435564 37435579 TCCAGTCAGTCAGCTGCCCTTGGGTCACAGCCACTGGGATCACAGCAGGGATTCCAAAGTGTAAA TCCAGTCAGTCAGCTGCCCTTGGGTCACAGC_______________AGGGATTCCAAAGTGTAAA TGCTGTGATCCCAGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37435576..37435750 26863196 MeRIP-seq:(Medium) rs1562114472 Functional Loss DEL dbSNP153 32..46 33 - - - 75934 RMVar_ID_75934 Human_SNP_ID_273464737 m1A Human chr6 + 37446424 37446424 37446424 TCTGACACTCCGGGGCTTTGACCAGGAGCTGAACGTGGACTGGCGAGATGAGCCAGAGGTAAGTG TCTGACACTCCGGGGCTTTGACCAGGAGCTGATCGTGGACTGGCGAGATGAGCCAGAGGTAAGTG A T CMTR1 Ensembl:ENSG00000137200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37446383..37446502 26863196 MeRIP-seq:(Medium) rs1440816568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970091,Human_RBP_ID_4888381,Human_RBP_ID_8905346,Human_RBP_ID_9400518,Human_RBP_ID_19016964,Human_RBP_ID_23067566 Human_Splice_Rec_766815,Human_Splice_Rec_766833 RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_333850,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_238201,RMVar_hsa_circ_266856,RMVar_hsa_circ_369196,RMVar_hsa_circ_238202,RMVar_hsa_circ_26975 75935 RMVar_ID_75935 Human_SNP_ID_273472443 m1A Human chr6 + 37478429 37478429 37478429 CGGGGAAATCAGGTTGGAGATGAAGATCATCAAGGGCTCCAGTGGCACCCCAAAGCTCAGCTACA CGGGGAAATCAGGTTGGAGATGAAGATCATCAGGGGCTCCAGTGGCACCCCAAAGCTCAGCTACA A G CMTR1 Ensembl:ENSG00000137200 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:37478426..37478500 32194978 MeRIP-seq:(Medium) rs1323511761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949560,Human_RBP_ID_3970106,Human_RBP_ID_8901253,Human_RBP_ID_9400520,Human_RBP_ID_15816264,Human_RBP_ID_18413788,Human_RBP_ID_19018524,Human_RBP_ID_26353947 Human_Splice_Rec_766868,Human_Splice_Rec_766869,Human_Splice_Rec_766884,Human_Splice_Rec_766885,Human_Splice_Rec_766892,Human_Splice_Rec_766893 RMVar_hsa_circ_238208,RMVar_hsa_circ_98062,RMVar_hsa_circ_343583,RMVar_hsa_circ_92120,RMVar_hsa_circ_102332,RMVar_hsa_circ_238214,RMVar_hsa_circ_70147,RMVar_hsa_circ_117652,RMVar_hsa_circ_120478,RMVar_hsa_circ_238216,RMVar_hsa_circ_238219,RMVar_hsa_circ_117288,RMVar_hsa_circ_238217,RMVar_hsa_circ_238218,RMVar_hsa_circ_128187,RMVar_hsa_circ_238220 75936 RMVar_ID_75936 Human_SNP_ID_273473694 m1A Human chr6 - 37483108 37483107 37483108 TGATCAGGATCAAGCAGGCACTTCAAGCCTCAATAGGACCAAGGTGCTGGGGTGTTCCCCTCCCA TGATCAGGATCAAGCAGGCACTTCAAGCCTCA_TAGGACCAAGGTGCTGGGGTGTTCCCCTCCCA AT A CCDC167 Ensembl:ENSG00000198937 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:37483014..37483110 32194978 MeRIP-seq:(Medium) rs1561796548 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_664011,Human_RBP_ID_9194213,Human_RBP_ID_17710760 Human_miRNA_ID_246777,Human_miRNA_ID_249310,Human_miRNA_ID_967776 75937 RMVar_ID_75937 Human_SNP_ID_273473695 m1A Human chr6 - 37483108 37483108 37483108 TGATCAGGATCAAGCAGGCACTTCAAGCCTCAATAGGACCAAGGTGCTGGGGTGTTCCCCTCCCA TGATCAGGATCAAGCAGGCACTTCAAGCCTCAGTAGGACCAAGGTGCTGGGGTGTTCCCCTCCCA T C CCDC167 Ensembl:ENSG00000198937 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:37483014..37483110 32194978 MeRIP-seq:(Medium) rs146381766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664011,Human_RBP_ID_9194213,Human_RBP_ID_17710760 Human_miRNA_ID_246777,Human_miRNA_ID_249310,Human_miRNA_ID_967776 75938 RMVar_ID_75938 Human_SNP_ID_273473737 m1A Human chr6 + 37483200 37483200 37483200 TGTGGGGAAGTGCCAGGCTCACATGGTCCAGTAGGCATAGACGAGCGTCAGGAGGATAAAGATGG TGTGGGGAAGTGCCAGGCTCACATGGTCCAGTGGGCATAGACGAGCGTCAGGAGGATAAAGATGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr6:37483151..37483317;chr6:37483176..37483200 26863196,32194978 MeRIP-seq:(Medium) rs775380039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15816357 75939 RMVar_ID_75939 Human_SNP_ID_273474222 m1A Human chr6 - 37484861 37484858 37484861 TTTGGTCCATGAAGCTCCTTTCCCCTCACAGGAGGTCCCTGGAGAAGGAGAAAAACAGCCTAATG TTTGGTCCATGAAGCTCCTTTCCCCTCACAGG___TCCCTGGAGAAGGAGAAAAACAGCCTAATG ACCT A CCDC167 Ensembl:ENSG00000198937 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37484801..37484875 26863196 MeRIP-seq:(Medium) rs1388110150 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4888480 Human_Splice_Rec_766900,Human_Splice_Rec_766901 75940 RMVar_ID_75940 Human_SNP_ID_273474348 m1A Human chr6 - 37485176 37485176 37485176 GGCCTTTGTTTCAGATCGATGGGCTAGAGGAGAAGCTGTCCCAGTGTCGGAGAGACCTGGAGGCC GGCCTTTGTTTCAGATCGATGGGCTAGAGGAGCAGCTGTCCCAGTGTCGGAGAGACCTGGAGGCC T G CCDC167 Ensembl:ENSG00000198937 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:37485126..37485200 26863196 MeRIP-seq:(Medium) rs1479445406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15816365,Human_RBP_ID_24161480 Human_Splice_Rec_766898,Human_Splice_Rec_766899 75941 RMVar_ID_75941 Human_SNP_ID_273477849 m1A Human chr6 + 37499774 37499774 37499774 CTATAGCCCAGCCTATCCCTTATCCCGCGGCCAGGAGAAGGCAACTAACGAGGTGGCCCAACCCC CTATAGCCCAGCCTATCCCTTATCCCGCGGCCGGGAGAAGGCAACTAACGAGGTGGCCCAACCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:37499770..37499875 26863196 MeRIP-seq:(Medium) rs568093346 Functional Loss SNV dbSNP153 33..33 33 - - - 75942 RMVar_ID_75942 Human_SNP_ID_273477880 m1A Human chr6 + 37499838 37499838 37499838 CCACTTTTCCCCTCACCTCTAGAGCGACGCCCAGATTCTCCCGCTTCTTTTTAGTCATGTTACTT CCACTTTTCCCCTCACCTCTAGAGCGACGCCCGGATTCTCCCGCTTCTTTTTAGTCATGTTACTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:37484781..37499849;chr6:37484819..37499875 26863196 MeRIP-seq:(Medium) rs1222090700 Functional Loss SNV dbSNP153 33..33 33 - - - 75943 RMVar_ID_75943 Human_SNP_ID_273527908 m1A Human chr6 - 37697621 37697621 37697621 CGAGCGGAGGCGGCGAGCGGCGCCCGCGCCGCAGCCCCGGCCTGGGCGAGAGCGCGAATATTTTT CGAGCGGAGGCGGCGAGCGGCGCCCGCGCCGCCGCCCCGGCCTGGGCGAGAGCGCGAATATTTTT T G MDGA1 Ensembl:ENSG00000112139 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37697584..37698015 26863196 MeRIP-seq:(Medium) rs1044832536 Functional Loss SNV dbSNP153 33..33 33 - - - 75944 RMVar_ID_75944 Human_SNP_ID_273528254 m1A Human chr6 - 37698209 37698204 37698209 AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGA AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAG_____GAGAGAGAGAGAGAGAGAGAGAGAAAGA CTCTCT C MDGA1 Ensembl:ENSG00000112139 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:37698200..37698282 26863410 MeRIP-seq:(Medium) rs1561870590 Functional Loss DEL dbSNP153 33..37 33 - - - 75945 RMVar_ID_75945 Human_SNP_ID_273528265 m1A Human chr6 - 37698209 37698208 37698209 AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGA AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAG_GAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGA CT C MDGA1 Ensembl:ENSG00000112139 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:37698200..37698282 26863410 MeRIP-seq:(Medium) rs1444689142 Functional Loss DEL dbSNP153 33..33 33 - - - 75946 RMVar_ID_75946 Human_SNP_ID_273528267 m1A Human chr6 - 37698209 37698209 37698209 AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGA AGAGAGAGAAAGAGAGAGAGAGAGAGAGAGAGCGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGA T G MDGA1 Ensembl:ENSG00000112139 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:37698200..37698282 26863410 MeRIP-seq:(Medium) rs960984468 Functional Loss SNV dbSNP153 33..33 33 - - - 75947 RMVar_ID_75947 Human_SNP_ID_273558474 m1A Human chr6 - 37819826 37819826 37819826 TCGGGGGGCTCGGGGCGGGGGGAGGGGGAAGGAGCGGGCGCGCGGGCGGGCGCGAGTCCGGGGCT TCGGGGGGCTCGGGGCGGGGGGAGGGGGAAGGGGCGGGCGCGCGGGCGGGCGCGAGTCCGGGGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:37819588..37819950 26863196 MeRIP-seq:(Medium) rs191064172 Functional Loss SNV dbSNP153 33..33 33 - - - 75948 RMVar_ID_75948 Human_SNP_ID_273558513 m1A Human chr6 + 37819880 37819880 37819880 GAGCCCCCCGACGCCGCCGCCACCGCCTCCTCAGAGCGGGGCCCGGGCCCAGCCGCCGCCACCGC GAGCCCCCCGACGCCGCCGCCACCGCCTCCTCTGAGCGGGGCCCGGGCCCAGCCGCCGCCACCGC A T ZFAND3 Ensembl:ENSG00000156639 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37819483..37819991 26863196 MeRIP-seq:(Medium) rs1171039305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4888675,Human_RBP_ID_9336148,Human_RBP_ID_17421714,Human_RBP_ID_22534107 Human_miRNA_ID_101090,Human_miRNA_ID_1386647,Human_miRNA_ID_2295152 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 75949 RMVar_ID_75949 Human_SNP_ID_273558522 m1A Human chr6 + 37819898 37819898 37819898 GCCACCGCCTCCTCAGAGCGGGGCCCGGGCCCAGCCGCCGCCACCGCTGCCGCCGCCGAGCTCCG GCCACCGCCTCCTCAGAGCGGGGCCCGGGCCCCGCCGCCGCCACCGCTGCCGCCGCCGAGCTCCG A C ZFAND3 Ensembl:ENSG00000156639 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,H2O2 treatment;HEK293T,untreat control chr6:37819797..37819947;chr6:37819754..37819947 26863410 MeRIP-seq:(Medium) rs961889587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9336148,Human_RBP_ID_17421714,Human_RBP_ID_22534107 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 75950 RMVar_ID_75950 Human_SNP_ID_273558530 m1A Human chr6 - 37819913 37819913 37819913 GGTGCTCGGCGGCGGCGGAGCTCGGCGGCGGCAGCGGTGGCGGCGGCTGGGCCCGGGCCCCGCTC GGTGCTCGGCGGCGGCGGAGCTCGGCGGCGGCGGCGGTGGCGGCGGCTGGGCCCGGGCCCCGCTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:37819662..37819980;chr6:37819726..37820000 26863196 MeRIP-seq:(Medium) rs912218182 Functional Loss SNV dbSNP153 33..33 33 - - - 75951 RMVar_ID_75951 Human_SNP_ID_273561631 m1A Human chr6 + 37831983 37831983 37831983 ATATGTTTCAAAAAAGTTAATGTGGAGGATGCATTGGAGTGTATAGGCAGAGAGACCAGTTAGAG ATATGTTTCAAAAAAGTTAATGTGGAGGATGCGTTGGAGTGTATAGGCAGAGAGACCAGTTAGAG A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:37831979..37832422 26863196 MeRIP-seq:(Medium) rs1268030074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7602498,Human_RBP_ID_15816856,Human_RBP_ID_24161592 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 75952 RMVar_ID_75952 Human_SNP_ID_273569374 m1A Human chr6 + 37861353 37861351 37861353 CTATCATAGTGTTGTAGATAAAGTGGGTATCAAGAGTGACTAGAAAAGGACACTGAAGAAATGAT CTATCATAGTGTTGTAGATAAAGTGGGTATC__GAGTGACTAGAAAAGGACACTGAAGAAATGAT CAA C ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37861348..37861467 26863196 MeRIP-seq:(Medium) rs1036102051 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15817743 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 75953 RMVar_ID_75953 Human_SNP_ID_273585583 m1A Human chr6 - 37924771 37924771 37924771 TCATTCTGTTGCCCAGACCAGAGTGCCCAATCATAGCTCACTGCAGCCTTGACCTCCTAGGCTCA TCATTCTGTTGCCCAGACCAGAGTGCCCAATCGTAGCTCACTGCAGCCTTGACCTCCTAGGCTCA T C lnc-MDGA1-4 RNACentral:URS00008B39C5 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37924769..37925044 26863196 MeRIP-seq:(Medium) rs1045422194 Functional Loss SNV dbSNP153 33..33 33 - - - 75954 RMVar_ID_75954 Human_SNP_ID_273605123 m1A Human chr6 + 38003782 38003782 38003782 CCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGAGAGCTACAGTGCCTGGCTAGTCCAGAA CCTGCCTCAGCCTCCCAAAGTGCTGGGATTACGGGCGAGAGCTACAGTGCCTGGCTAGTCCAGAA A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:38003779..38061688 32194978 MeRIP-seq:(Medium) rs1176468642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_767092 RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_342458,RMVar_hsa_circ_238230 75955 RMVar_ID_75955 Human_SNP_ID_273638963 m1A Human chr6 - 38138142 38138142 38138142 ATTTTTCTTTTTTTTTTCTTTCTTTAATAGAGACAAGGTCTCACTATGTTGCCCAGGTTGGTCTC ATTTTTCTTTTTTTTTTCTTTCTTTAATAGAGGCAAGGTCTCACTATGTTGCCCAGGTTGGTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38138137..38138267 26863196 MeRIP-seq:(Medium) rs1025092265 Functional Loss SNV dbSNP153 33..33 33 - - - 75956 RMVar_ID_75956 Human_SNP_ID_273642719 m1A Human chr6 + 38152966 38152965 38152967 TCTCCCACAGAGCTGGAAATGGGGGGTGGGGGACAGATTCTTACGGAAATTTTTTTACCTGACTT TCTCCCACAGAGCTGGAAATGGGGGGTGGGGG__AGATTCTTACGGAAATTTTTTTACCTGACTT GAC G ZFAND3 Ensembl:ENSG00000156639 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:38152801..38153628 32194978 MeRIP-seq:(Medium) rs778394939 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_664055,Human_RBP_ID_1047484,Human_RBP_ID_7604251,Human_RBP_ID_8216035,Human_RBP_ID_15821218,Human_RBP_ID_17420077 RMVar_hsa_circ_95998,RMVar_hsa_circ_238239 75957 RMVar_ID_75957 Human_SNP_ID_273642932 m1A Human chr6 + 38153712 38153710 38153712 GGGTGGGCCTGGTTGCCCCATGTTAGGAAATCACTACCAGTCAGGTGGGGCTGGGGCTGGGTGGA GGGTGGGCCTGGTTGCCCCATGTTAGGAAAT__CTACCAGTCAGGTGGGGCTGGGGCTGGGTGGA TCA T ZFAND3 Ensembl:ENSG00000156639 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:38153679..38153765 26863196 MeRIP-seq:(Medium) rs748713928 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_267214,Human_RBP_ID_664068,Human_RBP_ID_5152664,Human_RBP_ID_7663166,Human_RBP_ID_8215678,Human_RBP_ID_17710767,Human_RBP_ID_18075982,Human_RBP_ID_26536511 RMVar_hsa_circ_95998,RMVar_hsa_circ_238239 75958 RMVar_ID_75958 Human_SNP_ID_273642933 m1A Human chr6 + 38153712 38153712 38153712 GGGTGGGCCTGGTTGCCCCATGTTAGGAAATCACTACCAGTCAGGTGGGGCTGGGGCTGGGTGGA GGGTGGGCCTGGTTGCCCCATGTTAGGAAATCTCTACCAGTCAGGTGGGGCTGGGGCTGGGTGGA A T ZFAND3 Ensembl:ENSG00000156639 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:38153679..38153765 26863196 MeRIP-seq:(Medium) rs957736683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267214,Human_RBP_ID_664068,Human_RBP_ID_5152664,Human_RBP_ID_7663166,Human_RBP_ID_8215678,Human_RBP_ID_17710767,Human_RBP_ID_18075982,Human_RBP_ID_26536511 RMVar_hsa_circ_95998,RMVar_hsa_circ_238239 75959 RMVar_ID_75959 Human_SNP_ID_273644443 m1A Human chr6 + 38159000 38159000 38159000 AGAGACGGATGGAGGCTGTGCCTGGGGATGCCATCCAGAGGGACGGAGGAACCTGCAGAGGAGAC AGAGACGGATGGAGGCTGTGCCTGGGGATGCCGTCCAGAGGGACGGAGGAACCTGCAGAGGAGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38158949..38159074 26863196 MeRIP-seq:(Medium) rs1269171521 Functional Loss SNV dbSNP153 33..33 33 - - - 75960 RMVar_ID_75960 Human_SNP_ID_273705251 m1A Human chr6 + 38414644 38414644 38414644 CTTCCACCCCCACTACTCCATGGGATCTGTTCAGATATTTTTCAGCCCTGCTGACTGCTATGCAC CTTCCACCCCCACTACTCCATGGGATCTGTTCCGATATTTTTCAGCCCTGCTGACTGCTATGCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38414532..38414716 26863196 MeRIP-seq:(Medium) rs1397015570 Functional Loss SNV dbSNP153 33..33 33 - - - 75961 RMVar_ID_75961 Human_SNP_ID_273712288 m1A Human chr6 + 38443659 38443655 38443659 TCTCTTTGTCTCTCTCTCTCTTTCTCTCGCTCACTCATTTCCACCTCTTACCCACATGCACACAT TCTCTTTGTCTCTCTCTCTCTTTCTCTCG____CTCATTTCCACCTCTTACCCACATGCACACAT GCTCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38443482..38443719 26863196 MeRIP-seq:(Medium) rs1156424654 Functional Loss DEL dbSNP153 30..33 33 - - - 75962 RMVar_ID_75962 Human_SNP_ID_273725865 m1A Human chr6 + 38503331 38503331 38503331 AGGGCTGCTGCCCTCCCCCTTCTCTCCAGGAGACGGCCCAGGCTAATCTCTCCACCAAGACTTTA AGGGCTGCTGCCCTCCCCCTTCTCTCCAGGAGGCGGCCCAGGCTAATCTCTCCACCAAGACTTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:38503281..38503466 26863196 MeRIP-seq:(Medium) rs964123295 Functional Loss SNV dbSNP153 33..33 33 - - - 75963 RMVar_ID_75963 Human_SNP_ID_273725948 m1A Human chr6 + 38503660 38503660 38503660 GCTCCACCCACACCAGTCACCATTACCTACCAACTTCACACTCATCCCACCAAACTAAAAACTTA GCTCCACCCACACCAGTCACCATTACCTACCATCTTCACACTCATCCCACCAAACTAAAAACTTA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:38503609..38503717 26863196 MeRIP-seq:(Medium) rs1394093027 Functional Loss SNV dbSNP153 33..33 33 - - - 75964 RMVar_ID_75964 Human_SNP_ID_273726022 m1A Human chr6 + 38504015 38504015 38504015 CTTTGAACCTTCTAATCCACTGATCCCGCCACAGTCTCACAACCCCTTTCTGCCCTCATTTCCCT CTTTGAACCTTCTAATCCACTGATCCCGCCACCGTCTCACAACCCCTTTCTGCCCTCATTTCCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:38503969..38504075 26863196 MeRIP-seq:(Medium) rs1208787080 Functional Loss SNV dbSNP153 33..33 33 - - - 75965 RMVar_ID_75965 Human_SNP_ID_273726838 m1A Human chr6 - 38506962 38506959 38506962 CTTGGGTTATTCTAGAAGCCAGCAGGAACAGGAGGTTTTTATGGCCATAGTGAGGTGAGTTAGGG CTTGGGTTATTCTAGAAGCCAGCAGGAACAGG___TTTTTATGGCCATAGTGAGGTGAGTTAGGG ACCT A BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38506911..38507043 26863196 MeRIP-seq:(Medium) rs1302865431 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_67243 75966 RMVar_ID_75966 Human_SNP_ID_273729206 m1A Human chr6 - 38517699 38517699 38517699 GCTTTTTTCTGAAAGGGTTGCAAGGAGGAACTAAGAGTAGTCCTTGGAAAAGAGAAAGAAGGGGG GCTTTTTTCTGAAAGGGTTGCAAGGAGGAACTGAGAGTAGTCCTTGGAAAAGAGAAAGAAGGGGG T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:38517696..38517823 26863196 MeRIP-seq:(Medium) rs116162598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 75967 RMVar_ID_75967 Human_SNP_ID_273730850 m1A Human chr6 + 38525074 38525074 38525074 ATATTTTGTCACATGGGGGATATCATGATGGCACGATCAGCACTGATATGGTTTGGCTGTGTCCC ATATTTTGTCACATGGGGGATATCATGATGGCGCGATCAGCACTGATATGGTTTGGCTGTGTCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:38525070..38525202 26863196 MeRIP-seq:(Medium) rs944834556 Functional Loss SNV dbSNP153 33..33 33 - - - 75968 RMVar_ID_75968 Human_SNP_ID_273736124 m1A Human chr6 + 38547568 38547568 38547568 ATCCTTGTTTACTTGCTCCATCCACATTGTCCAACCTTTTGCTTTTCTCAGTTCTTTGAACCCAT ATCCTTGTTTACTTGCTCCATCCACATTGTCCGACCTTTTGCTTTTCTCAGTTCTTTGAACCCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38547540..38547714 26863196 MeRIP-seq:(Medium) rs887072826 Functional Loss SNV dbSNP153 33..33 33 - - - 75969 RMVar_ID_75969 Human_SNP_ID_273739791 m1A Human chr6 + 38563597 38563597 38563597 GATAGACTACCACAAGCTCTTTAACGTGCCCCACACACACATGCAGACCTGTACGACCTGGTCAT GATAGACTACCACAAGCTCTTTAACGTGCCCCCCACACACATGCAGACCTGTACGACCTGGTCAT A C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:38563560..38563727 26863196 MeRIP-seq:(Medium) rs1014988371 Functional Loss SNV dbSNP153 33..33 33 - - - 75970 RMVar_ID_75970 Human_SNP_ID_273756884 m1A Human chr6 - 38639896 38639870 38639897 CAGCAGCCGGGGCGGCGGCGAGGACGGCGGCCACGGAAGCGGCCAAGGGGGCGGTGGCGCAGAGA CAGCAGCCGGGGCGGCGGCGAGGACGGCGGC___________________________GCAGAGA CGCCACCGCCCCCTTGGCCGCTTCCGTG C BTBD9 Ensembl:ENSG00000183826 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38639695..38639940 26863196 MeRIP-seq:(Medium) rs1294834295 Functional Loss DEL dbSNP153 32..58 33 - - - Human_Splice_Rec_767131,Human_Splice_Rec_767151,Human_Splice_Rec_767229,Human_Splice_Rec_767233 RMVar_hsa_circ_114265,RMVar_hsa_circ_238250 75971 RMVar_ID_75971 Human_SNP_ID_273756892 m1A Human chr6 - 38639896 38639896 38639896 CAGCAGCCGGGGCGGCGGCGAGGACGGCGGCCACGGAAGCGGCCAAGGGGGCGGTGGCGCAGAGA CAGCAGCCGGGGCGGCGGCGAGGACGGCGGCCGCGGAAGCGGCCAAGGGGGCGGTGGCGCAGAGA T C BTBD9 Ensembl:ENSG00000183826 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:38639695..38639940 26863196 MeRIP-seq:(Medium) rs1201123912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_767131,Human_Splice_Rec_767151,Human_Splice_Rec_767229,Human_Splice_Rec_767233 RMVar_hsa_circ_114265,RMVar_hsa_circ_238250 75972 RMVar_ID_75972 Human_SNP_ID_273765633 m1A Human chr6 + 38677329 38677329 38677329 ACATTAAGGTTGCCATTTTGTTAGGATTCAAAATTTCAATCCAGTAGCCATCAGGATCTTGAATA ACATTAAGGTTGCCATTTTGTTAGGATTCAAATTTTCAATCCAGTAGCCATCAGGATCTTGAATA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:38677176..38677400 32194978 MeRIP-seq:(Medium) rs1265661864 Functional Loss SNV dbSNP153 33..33 33 - - - 75973 RMVar_ID_75973 Human_SNP_ID_273771601 m1A Human chr6 + 38703005 38703005 38703005 TGGTACTGGGGTCCGCGTCGGAGCAGCAACTGAGGGCGGCCTCGTCCGTGAGGCCGCCGGACGGG TGGTACTGGGGTCCGCGTCGGAGCAGCAACTGGGGGCGGCCTCGTCCGTGAGGCCGCCGGACGGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:38702951..38703150 26863196 MeRIP-seq:(Medium) rs751878828 Functional Loss SNV dbSNP153 33..33 33 - - - 75974 RMVar_ID_75974 Human_SNP_ID_273771614 m1A Human chr6 - 38703021 38703021 38703021 TGGCAGAACCGCAGCCCCCGTCCGGCGGCCTCACGGACGAGGCCGCCCTCAGTTGCTGCTCCGAC TGGCAGAACCGCAGCCCCCGTCCGGCGGCCTCTCGGACGAGGCCGCCCTCAGTTGCTGCTCCGAC T A GLO1 Ensembl:ENSG00000124767 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:38702951..38703125 26863196 MeRIP-seq:(Medium) rs756641310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251465,Human_RBP_ID_790196,Human_RBP_ID_1047541,Human_RBP_ID_4904010,Human_RBP_ID_5327451,Human_RBP_ID_5533060,Human_RBP_ID_9336149,Human_RBP_ID_18425912,Human_RBP_ID_22460698 Human_Splice_Rec_767241 RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 75975 RMVar_ID_75975 Human_SNP_ID_273771630 m1A Human chr6 - 38703063 38703063 38703063 CGTTCCTTGGGTCCCGTCGTCTGTGATACTGCAGCGCAGCCATGGCAGAACCGCAGCCCCCGTCC CGTTCCTTGGGTCCCGTCGTCTGTGATACTGCTGCGCAGCCATGGCAGAACCGCAGCCCCCGTCC T A GLO1 Ensembl:ENSG00000124767 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:38702951..38703150 26863410 MeRIP-seq:(Medium) rs1199014225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664170,Human_RBP_ID_790197,Human_RBP_ID_951999,Human_RBP_ID_1673164,Human_RBP_ID_4888865,Human_RBP_ID_5327451,Human_RBP_ID_5533060,Human_RBP_ID_8644932,Human_RBP_ID_9194473,Human_RBP_ID_9336149,Human_RBP_ID_15822911,Human_RBP_ID_17710786,Human_RBP_ID_18076181,Human_RBP_ID_18425912,Human_RBP_ID_18865489,Human_RBP_ID_22103620,Human_RBP_ID_22460698,Human_RBP_ID_24162374,Human_RBP_ID_26536594,Human_RBP_ID_27097965,Human_RBP_ID_27347055 Human_Splice_Rec_767241 RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 75976 RMVar_ID_75976 Human_SNP_ID_273771636 m1A Human chr6 + 38703076 38703076 38703076 GGTTCTGCCATGGCTGCGCTGCAGTATCACAGACGACGGGACCCAAGGAACGGAGGAGTCACCCA GGTTCTGCCATGGCTGCGCTGCAGTATCACAGGCGACGGGACCCAAGGAACGGAGGAGTCACCCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:38702951..38703150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 75977 RMVar_ID_75977 Human_SNP_ID_273771644 m1A Human chr6 + 38703088 38703088 38703088 GCTGCGCTGCAGTATCACAGACGACGGGACCCAAGGAACGGAGGAGTCACCCACACTACGCCTCG GCTGCGCTGCAGTATCACAGACGACGGGACCCCAGGAACGGAGGAGTCACCCACACTACGCCTCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:38702951..38703150;chr6:38703051..38703150 26863196 MeRIP-seq:(Medium) rs1354853595 Functional Loss SNV dbSNP153 33..33 33 - - - 75978 RMVar_ID_75978 Human_SNP_ID_273771655 m1A Human chr6 + 38703100 38703100 38703100 TATCACAGACGACGGGACCCAAGGAACGGAGGAGTCACCCACACTACGCCTCGGCCCTGTGCCGC TATCACAGACGACGGGACCCAAGGAACGGAGGCGTCACCCACACTACGCCTCGGCCCTGTGCCGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:38703051..38703125 32194978 MeRIP-seq:(Medium) rs1189600615 Functional Loss SNV dbSNP153 33..33 33 - - - 75979 RMVar_ID_75979 Human_SNP_ID_273871989 m1A Human chr6 + 39115042 39115042 39115042 CCCTGACTGGCAGCAGGGGGTTGGGCCGCCAGACCCGCCCGTTTCCGCGCCGCCCGAAACTCAGC CCCTGACTGGCAGCAGGGGGTTGGGCCGCCAGCCCCGCCCGTTTCCGCGCCGCCCGAAACTCAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:39114991..39115144 26863196 MeRIP-seq:(Medium) rs765339479 Functional Loss SNV dbSNP153 33..33 33 - - - 75980 RMVar_ID_75980 Human_SNP_ID_273899228 m1A Human chr6 - 39229409 39229409 39229409 TGGAGAAGCGGCCCACGTGTCTGCCCAGAGTCAAGTCCTGTGTTCTTCCCGCTCCTTACGCATCC TGGAGAAGCGGCCCACGTGTCTGCCCAGAGTCCAGTCCTGTGTTCTTCCCGCTCCTTACGCATCC T G KCNK5 Ensembl:ENSG00000164626 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:39229358..39229431 26863196 MeRIP-seq:(Medium) rs533457231 Functional Loss SNV dbSNP153 33..33 33 - - - 75981 RMVar_ID_75981 Human_SNP_ID_274051729 m1A Human chr6 - 39879315 39879315 39879315 GGGGCACCTGGGGGAGTCGGGGGTCCCCCGGGAGGAAGGGGTGGTGGTGGGGGAGGGGGACAACA GGGGCACCTGGGGGAGTCGGGGGTCCCCCGGGGGGAAGGGGTGGTGGTGGGGGAGGGGGACAACA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:39879227..39879371 26863410 MeRIP-seq:(Medium) rs1350186071 Functional Loss SNV dbSNP153 33..33 33 - - - 75982 RMVar_ID_75982 Human_SNP_ID_274072396 m1A Human chr6 - 39958627 39958627 39958627 GACACGGTGATGGCCACAGTCAAGAAAGGCAAACCAGAGCTCAGAAAAAAGGTACATCCAGCAGT GACACGGTGATGGCCACAGTCAAGAAAGGCAATCCAGAGCTCAGAAAAAAGGTACATCCAGCAGT T A FO393411.1 Ensembl:ENSG00000180211 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1049954854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1327517,Human_RBP_ID_1673178,Human_RBP_ID_8644961,Human_RBP_ID_10309243,Human_RBP_ID_15823013,Human_RBP_ID_17198835,Human_RBP_ID_17310552,Human_RBP_ID_17422269,Human_RBP_ID_17538272,Human_RBP_ID_17585108,Human_RBP_ID_17635223,Human_RBP_ID_17673977,Human_RBP_ID_18539305 75983 RMVar_ID_75983 Human_SNP_ID_274072397 m1A Human chr6 - 39958627 39958627 39958627 GACACGGTGATGGCCACAGTCAAGAAAGGCAAACCAGAGCTCAGAAAAAAGGTACATCCAGCAGT GACACGGTGATGGCCACAGTCAAGAAAGGCAAGCCAGAGCTCAGAAAAAAGGTACATCCAGCAGT T C FO393411.1 Ensembl:ENSG00000180211 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1049954854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1327517,Human_RBP_ID_1673178,Human_RBP_ID_8644961,Human_RBP_ID_10309243,Human_RBP_ID_15823013,Human_RBP_ID_17198835,Human_RBP_ID_17310552,Human_RBP_ID_17422269,Human_RBP_ID_17538272,Human_RBP_ID_17585108,Human_RBP_ID_17635223,Human_RBP_ID_17673977,Human_RBP_ID_18539305 75984 RMVar_ID_75984 Human_SNP_ID_274355203 m1A Human chr6 - 41073041 41073041 41073041 CCCCCGGTTCGCTGCCCGCGCTGATTGGCTCCAGTACCGGACTCCGAAACCCAATCAGAGGCTCC CCCCCGGTTCGCTGCCCGCGCTGATTGGCTCCCGTACCGGACTCCGAAACCCAATCAGAGGCTCC T G OARD1 Ensembl:ENSG00000124596 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41072991..41079100 26863196 MeRIP-seq:(Medium) rs1392729779 Functional Loss SNV dbSNP153 33..33 33 - - - 75985 RMVar_ID_75985 Human_SNP_ID_274359959 m1A Human chr6 + 41092965 41092965 41092965 GTGCCTGCTATCCAAAGAATCCCTCTACCTGGAGCAGAGATGCTTGAAGAAGAGCCTCTCTACGT GTGCCTGCTATCCAAAGAATCCCTCTACCTGGCGCAGAGATGCTTGAAGAAGAGCCTCTCTACGT A C NFYA Ensembl:ENSG00000001167 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr6:41091670..41094495;chr6:41091670..41092987 32194978 MeRIP-seq:(Medium) rs139182443 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_948238 Human_Splice_Rec_768760,Human_Splice_Rec_768776 Human_miRNA_ID_2742231 RMVar_hsa_circ_21701,RMVar_hsa_circ_345449,RMVar_hsa_circ_22459,RMVar_hsa_circ_105483,RMVar_hsa_circ_238297,RMVar_hsa_circ_34867,RMVar_hsa_circ_323916,RMVar_hsa_circ_354252,RMVar_hsa_circ_304684,RMVar_hsa_circ_238298,RMVar_hsa_circ_282963 75986 RMVar_ID_75986 Human_SNP_ID_274461267 m1A Human chr6 + 41504775 41504775 41504775 CTGTTCTCGTGTCAGTCTGCCCTGCCTCTGTTACTCCAAATCTCTGTGGTCTCTCTCCCTCTCTA CTGTTCTCGTGTCAGTCTGCCCTGCCTCTGTTCCTCCAAATCTCTGTGGTCTCTCTCCCTCTCTA A C LINC01276 Ensembl:ENSG00000226917 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:41504685..41504986 26863196 MeRIP-seq:(Medium) rs967773068 Functional Loss SNV dbSNP153 33..33 33 - - - 75987 RMVar_ID_75987 Human_SNP_ID_274461293 m1A Human chr6 - 41504891 41504890 41504892 ACACGAAGAGGGGCAGACAGAAAGGGACAGAGACATTCTCAGAGAGATAGCTTCAGAGACAAAGA ACACGAAGAGGGGCAGACAGAAAGGGACAGA__CATTCTCAGAGAGATAGCTTCAGAGACAAAGA GTC G FOXP4-AS1 Ensembl:ENSG00000234753 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41504672..41504982 26863196 MeRIP-seq:(Medium) rs1491231687 Functional Loss DEL dbSNP153 32..33 33 - - - 75988 RMVar_ID_75988 Human_SNP_ID_274471590 m1A Human chr6 + 41546148 41546148 41546148 TCTTCTCCCCACGTTCCCATTTTTCCTCCCCTAAAGTTTGGTGCACGTGGTTTTCTCTCGCTCTC TCTTCTCCCCACGTTCCCATTTTTCCTCCCCTGAAGTTTGGTGCACGTGGTTTTCTCTCGCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:41524143..41546249;chr6:41546069..41546231 26863196 MeRIP-seq:(Medium) rs1009271258 Functional Loss SNV dbSNP153 33..33 33 - - - 75989 RMVar_ID_75989 Human_SNP_ID_274471732 m1A Human chr6 + 41546528 41546528 41546528 GGCGCGGCGCAGGCGGCGGCGGCGCGGCGGGGAGGAGCCCGGGCCGGAACCAGGGCTGGGCCGGG GGCGCGGCGCAGGCGGCGGCGGCGCGGCGGGGTGGAGCCCGGGCCGGAACCAGGGCTGGGCCGGG A T FOXP4 Ensembl:ENSG00000137166 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:41546428..41546575 26863410 MeRIP-seq:(Medium) rs1055206050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903314,Human_RBP_ID_9354710 RMVar_hsa_circ_238303,RMVar_hsa_circ_118525 75990 RMVar_ID_75990 Human_SNP_ID_274471790 m1A Human chr6 + 41546651 41546651 41546651 AAGGACCGGGAAGGAAGAGCGGAGCCGGAGCGAGCCAAGCAGCCCACAAAGTGCCATGCCCCGGC AAGGACCGGGAAGGAAGAGCGGAGCCGGAGCGCGCCAAGCAGCCCACAAAGTGCCATGCCCCGGC A C FOXP4 Ensembl:ENSG00000137166 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr6:41546576..41546885;chr6:41546601..41546875 26863196 MeRIP-seq:(Medium) rs927432013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904856,Human_RBP_ID_5400736,Human_RBP_ID_18425642 RMVar_hsa_circ_238303,RMVar_hsa_circ_118525 75991 RMVar_ID_75991 Human_SNP_ID_274475353 m1A Human chr6 + 41560707 41560707 41560707 AAAACCCTGGTATTGTGCCTGTTTGGGGGAAGAAAACGTCAATAAAAATTAATTGATGAGTTGGC AAAACCCTGGTATTGTGCCTGTTTGGGGGAAGGAAACGTCAATAAAAATTAATTGATGAGTTGGC A G FOXP4 Ensembl:ENSG00000137166 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41560704..41560825 26863196 MeRIP-seq:(Medium) rs1033461243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22703306 RMVar_hsa_circ_238303,RMVar_hsa_circ_118525 75992 RMVar_ID_75992 Human_SNP_ID_274476604 m1A Human chr6 + 41565688 41565688 41565688 GGCGATGGTTATGTTTTTGGGGGTCAGCAGTCACTGCCCTTTCAGCCTTCAGCCTCAGCCTCTCC GGCGATGGTTATGTTTTTGGGGGTCAGCAGTCGCTGCCCTTTCAGCCTTCAGCCTCAGCCTCTCC A G FOXP4 Ensembl:ENSG00000137166 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41565686..41565950 26863196 MeRIP-seq:(Medium) rs557066803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238303,RMVar_hsa_circ_118525 75993 RMVar_ID_75993 Human_SNP_ID_274476605 m1A Human chr6 - 41565690 41565690 41565690 GGGGAGAGGCTGAGGCTGAAGGCTGAAAGGGCAGTGACTGCTGACCCCCAAAAACATAACCATCG GGGGAGAGGCTGAGGCTGAAGGCTGAAAGGGCGGTGACTGCTGACCCCCAAAAACATAACCATCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:41565687..41565953 26863196 MeRIP-seq:(Medium) rs1308368445 Functional Loss SNV dbSNP153 33..33 33 - - - 75994 RMVar_ID_75994 Human_SNP_ID_274476664 m1A Human chr6 - 41565819 41565819 41565819 TGCTGCCATCGGCTTGCCCAGAGAGGCTGCCCACGCCATTCTGACCAGATGGAGCCGACCTGATT TGCTGCCATCGGCTTGCCCAGAGAGGCTGCCCCCGCCATTCTGACCAGATGGAGCCGACCTGATT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:41565689..41565823 26863196 MeRIP-seq:(Medium) rs994596769 Functional Loss SNV dbSNP153 33..33 33 - - - 75995 RMVar_ID_75995 Human_SNP_ID_274482114 m1A Human chr6 + 41587121 41587121 41587121 GCAGAGGCAGGGGCTGGTCAGCCTGCAGCCCAACCAAGCCTCGGGGCCCCTCCAGACCCTTCCGC GCAGAGGCAGGGGCTGGTCAGCCTGCAGCCCAGCCAAGCCTCGGGGCCCCTCCAGACCCTTCCGC A G FOXP4 Ensembl:ENSG00000137166 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:41577997..41598802 32194978 MeRIP-seq:(Medium) rs749699849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21902981 Human_Splice_Rec_769065,Human_Splice_Rec_769097,Human_Splice_Rec_769129,Human_Splice_Rec_769161,Human_Splice_Rec_769191,Human_Splice_Rec_769217 RMVar_hsa_circ_70988,RMVar_hsa_circ_238303,RMVar_hsa_circ_118525,RMVar_hsa_circ_125755,RMVar_hsa_circ_326901,RMVar_hsa_circ_76759,RMVar_hsa_circ_238306,RMVar_hsa_circ_238307 75996 RMVar_ID_75996 Human_SNP_ID_274483124 m1A Human chr6 - 41590100 41590100 41590100 CGACGGGCTGGGCCCCCACCATGCAGGGAGGCAGAGCCCAGGCCAGGGGGCCGTAGAGGGGTGAC CGACGGGCTGGGCCCCCACCATGCAGGGAGGCCGAGCCCAGGCCAGGGGGCCGTAGAGGGGTGAC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:41589975..41590125 26863196 MeRIP-seq:(Medium) rs536802090 Functional Loss SNV dbSNP153 33..33 33 - - - 75997 RMVar_ID_75997 Human_SNP_ID_274485782 m1A Human chr6 + 41599013 41599013 41599013 CAGAATCCAGGCCCCATCTCCCCCAACTCCACAGCCCCTCCCGAGCCTCAAGGCAAGTCCAGGAC CAGAATCCAGGCCCCATCTCCCCCAACTCCACCGCCCCTCCCGAGCCTCAAGGCAAGTCCAGGAC A C FOXP4 Ensembl:ENSG00000137166 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41598965..41599432 26863196 MeRIP-seq:(Medium) rs892754661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664433,Human_RBP_ID_5216627,Human_RBP_ID_17090908,Human_RBP_ID_18076474 Human_miRNA_ID_466779,Human_miRNA_ID_876271,Human_miRNA_ID_1235635,Human_miRNA_ID_1561935 75998 RMVar_ID_75998 Human_SNP_ID_274485929 m1A Human chr6 - 41599522 41599518 41599522 CCTGCTCACACGGACCCCCACAGGGCACACAGACAGTCCCACCCCAGCAGCAGAGGGGGCTGTTT CCTGCTCACACGGACCCCCACAGGGCACACAG____TCCCACCCCAGCAGCAGAGGGGGCTGTTT ACTGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:41599472..41599569 26863196 MeRIP-seq:(Medium) rs1481338736 Functional Loss DEL dbSNP153 33..36 33 - - - 75999 RMVar_ID_75999 Human_SNP_ID_274486243 m1A Human chr6 - 41600476 41600476 41600476 GTATGTGGGGGGTTCTTGGGAAATATCCAAGGAGTCTTCTCAGTAAAGGGGCCAGGCCAGGGGTG GTATGTGGGGGGTTCTTGGGAAATATCCAAGGGGTCTTCTCAGTAAAGGGGCCAGGCCAGGGGTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:41600401..41600475 26863196 MeRIP-seq:(Medium) rs1393780261 Functional Loss SNV dbSNP153 33..33 33 - - - 76000 RMVar_ID_76000 Human_SNP_ID_274486247 m1A Human chr6 + 41600492 41600492 41600492 CCTTTACTGAGAAGACTCCTTGGATATTTCCCAAGAACCCCCCACATACACCCCTCACAAGCCAC CCTTTACTGAGAAGACTCCTTGGATATTTCCCGAGAACCCCCCACATACACCCCTCACAAGCCAC A G FOXP4 Ensembl:ENSG00000137166 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:41600343..41600583;chr6:41600443..41600593 26863196 MeRIP-seq:(Medium) rs1161234008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9194618,Human_RBP_ID_17091796,Human_RBP_ID_17310262,Human_RBP_ID_18958400,Human_RBP_ID_22424250 76001 RMVar_ID_76001 Human_SNP_ID_274496126 m1A Human chr6 - 41638705 41638705 41638705 TGCGGAAAACAGGGCTCAGCGGGCGGCGCCGGAGGCGGGCAAGGGGCGATTCCCCCGCAGATGCG TGCGGAAAACAGGGCTCAGCGGGCGGCGCCGGCGGCGGGCAAGGGGCGATTCCCCCGCAGATGCG T G lnc-TFEB-2 RNACentral:URS00008BB82A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41638661..41638824 26863196 MeRIP-seq:(Medium) rs558318212 Functional Loss SNV dbSNP153 33..33 33 - - - 76002 RMVar_ID_76002 Human_SNP_ID_274508591 m1A Human chr6 + 41684723 41684723 41684723 AGGCCAGCGGTAGCAGTGAGTCGTCCAGGAGCATGAGGTCCAGATCCTTCTTGGACAGGCTGGGG AGGCCAGCGGTAGCAGTGAGTCGTCCAGGAGCGTGAGGTCCAGATCCTTCTTGGACAGGCTGGGG A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41684599..41685003 26863196 MeRIP-seq:(Medium) rs1317959655 Functional Loss SNV dbSNP153 33..33 33 - - - 76003 RMVar_ID_76003 Human_SNP_ID_274508681 m1A Human chr6 + 41684906 41684906 41684906 GGGTGGGCAGGGGCAGCGGGGCTTGCGGGGGCAGAGCTGGCAGTGGCTCAGGGTCAGGGACCTCA GGGTGGGCAGGGGCAGCGGGGCTTGCGGGGGCGGAGCTGGCAGTGGCTCAGGGTCAGGGACCTCA A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41684730..41685069 26863196 MeRIP-seq:(Medium) rs930265945 Functional Loss SNV dbSNP153 33..33 33 - - - 76004 RMVar_ID_76004 Human_SNP_ID_274510191 m1A Human chr6 + 41690842 41690842 41690842 GTGGGCAGCAAACTTGTTCCCATAGGTCTCGGACAGGTACTCCCGCACCTTCTGATGCTGCGACT GTGGGCAGCAAACTTGTTCCCATAGGTCTCGGCCAGGTACTCCCGCACCTTCTGATGCTGCGACT A C RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:41689791..41691126 26863196 MeRIP-seq:(Medium) rs781007634 Functional Loss SNV dbSNP153 33..33 33 - - - 76005 RMVar_ID_76005 Human_SNP_ID_274517744 m1A Human chr6 - 41723173 41723173 41723173 AAGCTCTGGAGTGCAGGTTGGACAGCGTGGGAAATCAGGAGTCAGCCAGAGTTGTGCTTCAGTTT AAGCTCTGGAGTGCAGGTTGGACAGCGTGGGAGATCAGGAGTCAGCCAGAGTTGTGCTTCAGTTT T C TFEB Ensembl:ENSG00000112561 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41723171..41723256 26863196 MeRIP-seq:(Medium) rs888383611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821693,Human_RBP_ID_5656543,Human_RBP_ID_8215258,Human_RBP_ID_18957438,Human_RBP_ID_26793110 76006 RMVar_ID_76006 Human_SNP_ID_274530053 m1A Human chr6 - 41770673 41770673 41770673 GCCATGTCCAACCTGCAGAGAGCTCTGCCCCGAGACGATGGCACCGCCAGGAAAACCCGGCACAA GCCATGTCCAACCTGCAGAGAGCTCTGCCCCGCGACGATGGCACCGCCAGGAAAACCCGGCACAA T G FRS3 Ensembl:ENSG00000137218 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:41770622..41770727 26863196 MeRIP-seq:(Medium) rs1162906157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27568495 76007 RMVar_ID_76007 Human_SNP_ID_274530061 m1A Human chr6 - 41770702 41770702 41770702 ACGCCGTGATTGACCTCAAAAAGACCGTGGCCATGTCCAACCTGCAGAGAGCTCTGCCCCGAGAC ACGCCGTGATTGACCTCAAAAAGACCGTGGCCGTGTCCAACCTGCAGAGAGCTCTGCCCCGAGAC T C FRS3 Ensembl:ENSG00000137218 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41770651..41770718 26863196 MeRIP-seq:(Medium) rs759845275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664459 76008 RMVar_ID_76008 Human_SNP_ID_274535457 m1A Human chr6 - 41787734 41787734 41787734 GTTGTCCGGTATTTCGGGAGTTTCATTAGCCGAGCCAGCAGCGCTCACCGGGACAGTGCTGGAAG GTTGTCCGGTATTTCGGGAGTTTCATTAGCCGGGCCAGCAGCGCTCACCGGGACAGTGCTGGAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:41787651..41787853;chr6:41787651..41787864;chr6:41787676..41787874 26863196 MeRIP-seq:(Medium) rs1259171837 Functional Loss SNV dbSNP153 33..33 33 - - - 76009 RMVar_ID_76009 Human_SNP_ID_274560461 m1A Human chr6 - 41894800 41894800 41894800 AAAAGCCAGCCAAGGAGATAGGAAGGAGGCAAAAGCCAGGGTGGGCGTTAAGGAAGCCGGGCAGG AAAAGCCAGCCAAGGAGATAGGAAGGAGGCAATAGCCAGGGTGGGCGTTAAGGAAGCCGGGCAGG T A USP49 Ensembl:ENSG00000164663 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:41894749..41894938 26863196 MeRIP-seq:(Medium) rs1180113715 Functional Loss SNV dbSNP153 33..33 33 - - - 76010 RMVar_ID_76010 Human_SNP_ID_274567222 m1A Human chr6 + 41921748 41921748 41921748 CCCCGGCTGAGCCGACGGATTTTGCAGCAAGCACGGCAGCAACAGGAGGAACTCGAGGCCGAGCA CCCCGGCTGAGCCGACGGATTTTGCAGCAAGCGCGGCAGCAACAGGAGGAACTCGAGGCCGAGCA A G BYSL Ensembl:ENSG00000112578 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:41921550..41921850 26863196 MeRIP-seq:(Medium) rs769293717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79736,Human_RBP_ID_841632,Human_RBP_ID_949586,Human_RBP_ID_5400773,Human_RBP_ID_22460708 Human_Splice_Rec_769711,Human_Splice_Rec_769723,Human_Splice_Rec_769725,Human_Splice_Rec_769735 RMVar_hsa_circ_98970,RMVar_hsa_circ_238332 76011 RMVar_ID_76011 Human_SNP_ID_274571182 m1A Human chr6 - 41935978 41935978 41935978 CCCGGGGCTCCAGCAGCCAAGGGCCCAGCCAGACCAGCACTCCTACAGATGTCACAGCCATACAC CCCGGGGCTCCAGCAGCCAAGGGCCCAGCCAGCCCAGCACTCCTACAGATGTCACAGCCATACAC T G CCND3 Ensembl:ENSG00000112576 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41935928..41936037 26863196 MeRIP-seq:(Medium) rs1396089018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1111758 Human_miRNA_ID_2330970,Human_miRNA_ID_2773978,Human_miRNA_ID_2964052 RMVar_hsa_circ_75750,RMVar_hsa_circ_238337 76012 RMVar_ID_76012 Human_SNP_ID_274571204 m1A Human chr6 - 41936024 41936024 41936024 CTCAGGGAAGCCTCTCAGACCAGCTCCAGCCCAGCGCCCAAAGCCCCCCGGGGCTCCAGCAGCCA CTCAGGGAAGCCTCTCAGACCAGCTCCAGCCCGGCGCCCAAAGCCCCCCGGGGCTCCAGCAGCCA T C CCND3 Ensembl:ENSG00000112576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:41935976..41936261 32194978 MeRIP-seq:(Medium) rs990076942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1111759 Human_Splice_Rec_769756,Human_Splice_Rec_769762,Human_Splice_Rec_769770,Human_Splice_Rec_769778,Human_Splice_Rec_769784,Human_Splice_Rec_769792,Human_Splice_Rec_769798,Human_Splice_Rec_769804,Human_Splice_Rec_769808 Human_miRNA_ID_2553239 RMVar_hsa_circ_75750,RMVar_hsa_circ_238337 76013 RMVar_ID_76013 Human_SNP_ID_274571558 m1A Human chr6 - 41937291 41937291 41937291 CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGACCGACAGGCCTTGGTCAAAAAGCATGCCCAGA CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGGCCGACAGGCCTTGGTCAAAAAGCATGCCCAGA T C CCND3 Ensembl:ENSG00000112576 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:41937190..41937291 32194978 MeRIP-seq:(Medium) rs147099303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789889,Human_RBP_ID_8901476,Human_RBP_ID_9309300,Human_RBP_ID_17710827,Human_RBP_ID_18195590 Human_Splice_Rec_769753,Human_Splice_Rec_769759,Human_Splice_Rec_769767,Human_Splice_Rec_769775,Human_Splice_Rec_769781,Human_Splice_Rec_769789,Human_Splice_Rec_769795,Human_Splice_Rec_769803,Human_Splice_Rec_769807,Human_Splice_Rec_769811,Human_Splice_Rec_769815,Human_Splice_Rec_769819,Human_Splice_Rec_769825,Human_Splice_Rec_769829 Human_miRNA_ID_2225068 RMVar_hsa_circ_92809,RMVar_hsa_circ_75750,RMVar_hsa_circ_238337,RMVar_hsa_circ_238339,RMVar_hsa_circ_238338,RMVar_hsa_circ_372050 76014 RMVar_ID_76014 Human_SNP_ID_274571559 m1A Human chr6 - 41937291 41937291 41937291 CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGACCGACAGGCCTTGGTCAAAAAGCATGCCCAGA CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGCCCGACAGGCCTTGGTCAAAAAGCATGCCCAGA T G CCND3 Ensembl:ENSG00000112576 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:41937190..41937291 32194978 MeRIP-seq:(Medium) rs147099303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789889,Human_RBP_ID_8901476,Human_RBP_ID_9309300,Human_RBP_ID_17710827,Human_RBP_ID_18195590 Human_Splice_Rec_769753,Human_Splice_Rec_769759,Human_Splice_Rec_769767,Human_Splice_Rec_769775,Human_Splice_Rec_769781,Human_Splice_Rec_769789,Human_Splice_Rec_769795,Human_Splice_Rec_769803,Human_Splice_Rec_769807,Human_Splice_Rec_769811,Human_Splice_Rec_769815,Human_Splice_Rec_769819,Human_Splice_Rec_769825,Human_Splice_Rec_769829 Human_miRNA_ID_2225068 RMVar_hsa_circ_92809,RMVar_hsa_circ_75750,RMVar_hsa_circ_238337,RMVar_hsa_circ_238339,RMVar_hsa_circ_238338,RMVar_hsa_circ_372050 76015 RMVar_ID_76015 Human_SNP_ID_274572575 m1A Human chr6 + 41941409 41941409 41941409 GGATGTCCCGACAGGGCGGCCCCGGTGTGTCCAGACCCGGGAGCGGTGGGGGAGGGGGACGCGTC GGATGTCCCGACAGGGCGGCCCCGGTGTGTCCGGACCCGGGAGCGGTGGGGGAGGGGGACGCGTC A G RF00017-4499,RF00017-4494 RNACentral:URS000098B860,RNACentral:URS00009086DB SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:41941407..41941755 32194978 MeRIP-seq:(Medium) rs758087276 Functional Loss SNV dbSNP153 33..33 33 - - - 76016 RMVar_ID_76016 Human_SNP_ID_274572632 m1A Human chr6 + 41941549 41941549 41941549 AGTAGGAGGCGCGGGGTACGTAGCGCTCCTCCAGGCGGAGCAGGCTCTGCAGGACACGCTGGTCC AGTAGGAGGCGCGGGGTACGTAGCGCTCCTCCTGGCGGAGCAGGCTCTGCAGGACACGCTGGTCC A T RF00017-4499,RF00017-4494 RNACentral:URS000098B860,RNACentral:URS00009086DB SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:41941503..41941812 26863196 MeRIP-seq:(Medium) rs1341839947 Functional Loss SNV dbSNP153 33..33 33 - - - 76017 RMVar_ID_76017 Human_SNP_ID_274572644 m1A Human chr6 - 41941576 41941576 41941576 GGCCGGGCCGGACCCGCGGCTGCTGGGGGACCAGCGTGTCCTGCAGAGCCTGCTCCGCCTGGAGG GGCCGGGCCGGACCCGCGGCTGCTGGGGGACCGGCGTGTCCTGCAGAGCCTGCTCCGCCTGGAGG T C CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:41941526..41941781 26863196 MeRIP-seq:(Medium) rs1374056626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252081,Human_RBP_ID_664567,Human_RBP_ID_4904863,Human_RBP_ID_8905814,Human_RBP_ID_9336665,Human_RBP_ID_22534108 76018 RMVar_ID_76018 Human_SNP_ID_274601839 m1A Human chr6 + 42057470 42057470 42057470 GAACCGACCCCACCCGCCGCACATCCCCAGCCATTTTCCTGAGTTCCCTGATCCCCACACCTACA GAACCGACCCCACCCGCCGCACATCCCCAGCCGTTTTCCTGAGTTCCCTGATCCCCACACCTACA A G TAF8 Ensembl:ENSG00000137413 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42057420..42057533 26863196 MeRIP-seq:(Medium) rs757874607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9400536,Human_RBP_ID_18958410,Human_RBP_ID_27524743 Human_Splice_Rec_769866,Human_Splice_Rec_769874,Human_Splice_Rec_769875,Human_Splice_Rec_769892,Human_Splice_Rec_769893,Human_Splice_Rec_769908,Human_Splice_Rec_769909,Human_Splice_Rec_769932,Human_Splice_Rec_769933,Human_Splice_Rec_769950,Human_Splice_Rec_769951,Human_Splice_Rec_769960,Human_Splice_Rec_769961 Human_miRNA_ID_1509306,Human_miRNA_ID_2770140 RMVar_hsa_circ_34252,RMVar_hsa_circ_64717,RMVar_hsa_circ_326800,RMVar_hsa_circ_113407,RMVar_hsa_circ_238342,RMVar_hsa_circ_238343,RMVar_hsa_circ_238344,RMVar_hsa_circ_378991 76019 RMVar_ID_76019 Human_SNP_ID_274601847 m1A Human chr6 + 42057488 42057488 42057488 GCACATCCCCAGCCATTTTCCTGAGTTCCCTGATCCCCACACCTACATCAAAACTCCGGTGAGTG GCACATCCCCAGCCATTTTCCTGAGTTCCCTGGTCCCCACACCTACATCAAAACTCCGGTGAGTG A G TAF8 Ensembl:ENSG00000137413 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42057353..42057527 26863196 MeRIP-seq:(Medium) rs369886097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9194658,Human_RBP_ID_9400536,Human_RBP_ID_15826866,Human_RBP_ID_17307228,Human_RBP_ID_17420192,Human_RBP_ID_18076593,Human_RBP_ID_18958410,Human_RBP_ID_27524743 Human_Splice_Rec_769866,Human_Splice_Rec_769874,Human_Splice_Rec_769875,Human_Splice_Rec_769892,Human_Splice_Rec_769893,Human_Splice_Rec_769908,Human_Splice_Rec_769909,Human_Splice_Rec_769932,Human_Splice_Rec_769933,Human_Splice_Rec_769950,Human_Splice_Rec_769951,Human_Splice_Rec_769960,Human_Splice_Rec_769961 Human_miRNA_ID_2725221 RMVar_hsa_circ_34252,RMVar_hsa_circ_64717,RMVar_hsa_circ_326800,RMVar_hsa_circ_113407,RMVar_hsa_circ_238342,RMVar_hsa_circ_238343,RMVar_hsa_circ_238344,RMVar_hsa_circ_378991 76020 RMVar_ID_76020 Human_SNP_ID_274605849 m1A Human chr6 - 42073511 42073511 42073511 CCTACTCCGAGCACCCCACTTAAAAACTGAAGACTCCTCCTCACCCTGGATCTTCCCCTACTGTT CCTACTCCGAGCACCCCACTTAAAAACTGAAGCCTCCTCCTCACCCTGGATCTTCCCCTACTGTT T G RF00017-4541,RF00017-1287 RNACentral:URS0000992647,RNACentral:URS000098E119 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42073499..42073630 26863196 MeRIP-seq:(Medium) rs1392704467 Functional Loss SNV dbSNP153 33..33 33 - - - 76021 RMVar_ID_76021 Human_SNP_ID_274607413 m1A Human chr6 + 42079637 42079637 42079637 CCAGCTGGAGTATAGTGGCACTACCTCGGCTCACTGCAACCTCCACTCCCCGGGTTCAAGCAATT CCAGCTGGAGTATAGTGGCACTACCTCGGCTCGCTGCAACCTCCACTCCCCGGGTTCAAGCAATT A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1314704346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7606869,Human_RBP_ID_27524748 Human_miRNA_ID_867714 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 76022 RMVar_ID_76022 Human_SNP_ID_274638290 m1A Human chr6 + 42196856 42196856 42196856 CTCCAAATGGCCTTTTACTTTTTTCTCCCCAAAAAAGGCCAGTCCCTTTGAAGCCACATCTGACT CTCCAAATGGCCTTTTACTTTTTTCTCCCCAAGAAAGGCCAGTCCCTTTGAAGCCACATCTGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42196806..42196893 26863196 MeRIP-seq:(Medium) rs955258191 Functional Loss SNV dbSNP153 33..33 33 - - - 76023 RMVar_ID_76023 Human_SNP_ID_274639251 m1A Human chr6 - 42200591 42200589 42200592 TCTGGGCGAGAATGTCAGGAATGGAGGTGAGGAGAAGTGGTTTGATTTAGAGTATAGTTTGCAGG TCTGGGCGAGAATGTCAGGAATGGAGGTGAG___AAGTGGTTTGATTTAGAGTATAGTTTGCAGG TCTC T RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42200540..42200851 26863196 MeRIP-seq:(Medium) rs1160799690 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_15827698,Human_RBP_ID_24163254 76024 RMVar_ID_76024 Human_SNP_ID_274639255 m1A Human chr6 + 42200609 42200609 42200609 AATCAAACCACTTCTCCTCACCTCCATTCCTGACATTCTCGCCCAGACCAGCATCATCTCACCTG AATCAAACCACTTCTCCTCACCTCCATTCCTGGCATTCTCGCCCAGACCAGCATCATCTCACCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42200523..42200826 26863196 MeRIP-seq:(Medium) rs115032690 Functional Loss SNV dbSNP153 33..33 33 - - - 76025 RMVar_ID_76025 Human_SNP_ID_274654045 m1A Human chr6 - 42259593 42259593 42259593 CTTCATCCCGCCGCCGCCCTCCTACAACCCGAACCCCGCTGCCTCCTACTCGGGCGCCACCCTGT CTTCATCCCGCCGCCGCCCTCCTACAACCCGATCCCCGCTGCCTCCTACTCGGGCGCCACCCTGT T A TRERF1 Ensembl:ENSG00000124496 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42259546..42259636 26863196 MeRIP-seq:(Medium) rs752427096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3491,RMVar_hsa_circ_238357,RMVar_hsa_circ_123860,RMVar_hsa_circ_67930,RMVar_hsa_circ_377231 76026 RMVar_ID_76026 Human_SNP_ID_274654046 m1A Human chr6 - 42259593 42259593 42259593 CTTCATCCCGCCGCCGCCCTCCTACAACCCGAACCCCGCTGCCTCCTACTCGGGCGCCACCCTGT CTTCATCCCGCCGCCGCCCTCCTACAACCCGAGCCCCGCTGCCTCCTACTCGGGCGCCACCCTGT T C TRERF1 Ensembl:ENSG00000124496 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42259546..42259636 26863196 MeRIP-seq:(Medium) rs752427096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3491,RMVar_hsa_circ_238357,RMVar_hsa_circ_123860,RMVar_hsa_circ_67930,RMVar_hsa_circ_377231 76027 RMVar_ID_76027 Human_SNP_ID_274672897 m1A Human chr6 - 42335800 42335800 42335800 AGATGGAGTAGAGGAAACTATGTCAGCACGCAATGGAAGCTAGACTTTGTTTTGGGGAGTCAGAG AGATGGAGTAGAGGAAACTATGTCAGCACGCAGTGGAAGCTAGACTTTGTTTTGGGGAGTCAGAG T C TRERF1 Ensembl:ENSG00000124496 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42335794..42335859 26863196 MeRIP-seq:(Medium) rs538536017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11291,RMVar_hsa_circ_238367 76028 RMVar_ID_76028 Human_SNP_ID_274698158 m1A Human chr6 + 42444736 42444736 42444736 GATCAGTCACTCCCTCTCCACTGATCTTTCCCATCAGCACACAAATTACCAACACTTCCAAAAAA GATCAGTCACTCCCTCTCCACTGATCTTTCCCGTCAGCACACAAATTACCAACACTTCCAAAAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42444712..42444946 26863196 MeRIP-seq:(Medium) rs903898398 Functional Loss SNV dbSNP153 33..33 33 - - - 76029 RMVar_ID_76029 Human_SNP_ID_274700079 m1A Human chr6 - 42452412 42452412 42452412 CCGCCGTAGCGCTGCGCCCCGGGGGAAAGGGGACGCGGGCGGGGGCCGAGGCGGACGACCAGCCG CCGCCGTAGCGCTGCGCCCCGGGGGAAAGGGGGCGCGGGCGGGGGCCGAGGCGGACGACCAGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42452364..42452509 26863196 MeRIP-seq:(Medium) rs1279602932 Functional Loss SNV dbSNP153 33..33 33 - - - 76030 RMVar_ID_76030 Human_SNP_ID_274727961 m1A Human chr6 + 42564090 42564090 42564090 GGTTTTCTGTGTCCTTCCCTGGGTCAGGGACGAGCCAGTGACTTGACTCTTGGGCGCTAAGCTTG GGTTTTCTGTGTCCTTCCCTGGGTCAGGGACGGGCCAGTGACTTGACTCTTGGGCGCTAAGCTTG A G UBR2 Ensembl:ENSG00000024048 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42564041..42564167 26863196 MeRIP-seq:(Medium) rs946182072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904030,Human_RBP_ID_9336669,Human_RBP_ID_22462742 76031 RMVar_ID_76031 Human_SNP_ID_274773265 m1A Human chr6 + 42745508 42745508 42745508 CGCTGGCTCTCTTCTCCAAGACTTGGGACTCCAGGTTGGAGAAACCGCAGACCCAGCTGGGGCCG CGCTGGCTCTCTTCTCCAAGACTTGGGACTCCGGGTTGGAGAAACCGCAGACCCAGCTGGGGCCG A G RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:42745459..42745704 32194978 MeRIP-seq:(Medium) rs961548023 Functional Loss SNV dbSNP153 33..33 33 - - - 76032 RMVar_ID_76032 Human_SNP_ID_274773526 m1A Human chr6 + 42746022 42746022 42746022 CCGCTCAGGCACCAGGCTCAGGTCCCGCTGGGACTCCATGTCTCCGGTCCTGACAGCAGCAGCGG CCGCTCAGGCACCAGGCTCAGGTCCCGCTGGGCCTCCATGTCTCCGGTCCTGACAGCAGCAGCGG A C RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:42745923..42746047 26863410 MeRIP-seq:(Medium) rs1314385549 Functional Loss SNV dbSNP153 33..33 33 - - - 76033 RMVar_ID_76033 Human_SNP_ID_274773545 m1A Human chr6 + 42746044 42746042 42746045 TCCCGCTGGGACTCCATGTCTCCGGTCCTGACAGCAGCAGCGGAGCAACTGACGGACTCCATATT TCCCGCTGGGACTCCATGTCTCCGGTCCTGA___CAGCAGCGGAGCAACTGACGGACTCCATATT ACAG A RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42745801..42746100 26863196 MeRIP-seq:(Medium) rs552676046 Functional Loss DEL dbSNP153 32..34 33 - - - 76034 RMVar_ID_76034 Human_SNP_ID_274773547 m1A Human chr6 + 42746044 42746044 42746044 TCCCGCTGGGACTCCATGTCTCCGGTCCTGACAGCAGCAGCGGAGCAACTGACGGACTCCATATT TCCCGCTGGGACTCCATGTCTCCGGTCCTGACGGCAGCAGCGGAGCAACTGACGGACTCCATATT A G RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42745801..42746100 26863196 MeRIP-seq:(Medium) rs750349817 Functional Loss SNV dbSNP153 33..33 33 - - - 76035 RMVar_ID_76035 Human_SNP_ID_274775893 m1A Human chr6 + 42755054 42755054 42755054 GGTAGATGACTCTGATAGTTTCTGCGTCCTCTATAAAGCAGACAGTGAGGTCTCATGCTGAGTAT GGTAGATGACTCTGATAGTTTCTGCGTCCTCTGTAAAGCAGACAGTGAGGTCTCATGCTGAGTAT A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42755045..42755248 26863196 MeRIP-seq:(Medium) rs371546746 Functional Loss SNV dbSNP153 33..33 33 - - - 76036 RMVar_ID_76036 Human_SNP_ID_274782216 m1A Human chr6 - 42781881 42781881 42781881 GCCCGCCCGGCCTTCATGCTCTGCGCCCGGGCAAACCGCTCGCCTGCTCGTCTACCTCCAAACTT GCCCGCCCGGCCTTCATGCTCTGCGCCCGGGCGAACCGCTCGCCTGCTCGTCTACCTCCAAACTT T C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:42781864..42782060;chr6:42781825..42782076 26863196 MeRIP-seq:(Medium) rs1328143862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5276810 76037 RMVar_ID_76037 Human_SNP_ID_274784979 m1A Human chr6 + 42790829 42790829 42790829 GCATGGCTCTTGCTTGATGAATAATGTTCTGTATAGTAGAAGAGGAAAATACAGTGAGTGAAGGA GCATGGCTCTTGCTTGATGAATAATGTTCTGTGTAGTAGAAGAGGAAAATACAGTGAGTGAAGGA A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42790778..42790956 26863196 MeRIP-seq:(Medium) rs1281783037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238475,RMVar_hsa_circ_43053,RMVar_hsa_circ_287232,RMVar_hsa_circ_315542,RMVar_hsa_circ_238476,RMVar_hsa_circ_238477,RMVar_hsa_circ_95413 76038 RMVar_ID_76038 Human_SNP_ID_274798075 m1A Human chr6 + 42844685 42844685 42844685 CTTGTTTCTGTGGAATGGTAGGTGCAGAAGCCAGATGGCAACAGACTGAGGAGAGAGCAGGAGGT CTTGTTTCTGTGGAATGGTAGGTGCAGAAGCCGGATGGCAACAGACTGAGGAGAGAGCAGGAGGT A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42844671..42844751 26863196 MeRIP-seq:(Medium) rs1158832199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43053,RMVar_hsa_circ_238476,RMVar_hsa_circ_324197,RMVar_hsa_circ_238480,RMVar_hsa_circ_293380,RMVar_hsa_circ_267047,RMVar_hsa_circ_332559,RMVar_hsa_circ_44225,RMVar_hsa_circ_265805,RMVar_hsa_circ_238482 76039 RMVar_ID_76039 Human_SNP_ID_274807192 m1A Human chr6 - 42879959 42879956 42879960 CAAGACCCCACTCCAGATATTCAAAGCCCCAAACACTCACTCTTGCTCCGCCATCTTTCTAGTGG CAAGACCCCACTCCAGATATTCAAAGCCCCA____CTCACTCTTGCTCCGCCATCTTTCTAGTGG GTGTT G RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42879946..42880253 26863196 MeRIP-seq:(Medium) rs1488444862 Functional Loss DEL dbSNP153,HGVD 32..35 33 - - - 76040 RMVar_ID_76040 Human_SNP_ID_274807194 m1A Human chr6 - 42879959 42879959 42879959 CAAGACCCCACTCCAGATATTCAAAGCCCCAAACACTCACTCTTGCTCCGCCATCTTTCTAGTGG CAAGACCCCACTCCAGATATTCAAAGCCCCAATCACTCACTCTTGCTCCGCCATCTTTCTAGTGG T A RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42879946..42880253 26863196 MeRIP-seq:(Medium) rs759292375 Functional Loss SNV dbSNP153 33..33 33 - - - 76041 RMVar_ID_76041 Human_SNP_ID_274807195 m1A Human chr6 - 42879959 42879959 42879959 CAAGACCCCACTCCAGATATTCAAAGCCCCAAACACTCACTCTTGCTCCGCCATCTTTCTAGTGG CAAGACCCCACTCCAGATATTCAAAGCCCCAAGCACTCACTCTTGCTCCGCCATCTTTCTAGTGG T C RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42879946..42880253 26863196 MeRIP-seq:(Medium) rs759292375 Functional Loss SNV dbSNP153 33..33 33 - - - 76042 RMVar_ID_76042 Human_SNP_ID_274808127 m1A Human chr6 + 42882951 42882951 42882951 AACAAGGAGTGAGGTCTTGTGTTACCCAGGCTAGAGTGCAGTGGCAGGATCATAGCTCATTGCAG AACAAGGAGTGAGGTCTTGTGTTACCCAGGCTGGAGTGCAGTGGCAGGATCATAGCTCATTGCAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs977879657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7607862 RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 76043 RMVar_ID_76043 Human_SNP_ID_274809401 m1A Human chr6 + 42887319 42887319 42887319 AAAAGACAGTAGCTGGCCGGTCGTGGTGGCTCATGCCTGTAATCCCAACACTTAGGGAGGCTGAG AAAAGACAGTAGCTGGCCGGTCGTGGTGGCTCGTGCCTGTAATCCCAACACTTAGGGAGGCTGAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42887268..42887382 26863196 MeRIP-seq:(Medium) rs1562513995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829817,Human_RBP_ID_24163577,Human_RBP_ID_26539496 Human_miRNA_ID_1062495 76044 RMVar_ID_76044 Human_SNP_ID_274809623 m1A Human chr6 + 42888216 42888216 42888216 TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTG TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCGTGATCTCAGCTCATTGCAGCCTCCACCTCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878875910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252300,Human_RBP_ID_664709 76045 RMVar_ID_76045 Human_SNP_ID_274809625 m1A Human chr6 + 42888224 42888224 42888224 TTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAG TTGCCCAGGCTGGAGCGCAGTGGCATGATCTCGGCTCATTGCAGCCTCCACCTCCTGGGTTCAAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11558567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252300,Human_RBP_ID_27347399 76046 RMVar_ID_76046 Human_SNP_ID_274809628 m1A Human chr6 + 42888234 42888234 42888234 TGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC TGGAGCGCAGTGGCATGATCTCAGCTCATTGCGGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1167593296 Functional Loss SNV dbSNP153 33..33 33 - - - 76047 RMVar_ID_76047 Human_SNP_ID_274809642 m1A Human chr6 + 42888291 42888291 42888291 ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTT ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTGCATGCATGTACCACCACACCCAGCTAATTCTT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1318315394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4890182 76048 RMVar_ID_76048 Human_SNP_ID_274809664 m1A Human chr6 + 42888367 42888367 42888367 AGAGATGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATC AGAGATGGAGACAGAGTTTCACCATGTAGGCCGGGCTAGTCTCAAACTCCTGACCTCAAGTGATC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1304984453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 76049 RMVar_ID_76049 Human_SNP_ID_274809665 m1A Human chr6 + 42888372 42888372 42888372 TGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCACAA TGGAGACAGAGTTTCACCATGTAGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1226897826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 76050 RMVar_ID_76050 Human_SNP_ID_274809668 m1A Human chr6 + 42888379 42888379 42888379 AGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCACAAGCCTGGG AGAGTTTCACCATGTAGGCCAGGCTAGTCTCAGACTCCTGACCTCAAGTGATCCACAAGCCTGGG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs569236566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 76051 RMVar_ID_76051 Human_SNP_ID_274809735 m1A Human chr6 + 42888592 42888592 42888592 CAAGATAGATTTTTCCCTTCATAGTGGCAGATAGTGTTAACCCCTGCACCATCTGTAACTCAGAA CAAGATAGATTTTTCCCTTCATAGTGGCAGATGGTGTTAACCCCTGCACCATCTGTAACTCAGAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1055969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664712,Human_RBP_ID_7607912,Human_RBP_ID_15829834,Human_RBP_ID_17307251,Human_RBP_ID_17420216,Human_RBP_ID_17536297,Human_RBP_ID_18076787,Human_RBP_ID_18371459,Human_RBP_ID_18958417,Human_RBP_ID_23195641,Human_RBP_ID_24163582,Human_RBP_ID_26536826,Human_RBP_ID_27756207 Human_miRNA_ID_289991,Human_miRNA_ID_528010 76052 RMVar_ID_76052 Human_SNP_ID_274809860 m1A Human chr6 + 42889199 42889199 42889199 ACGGTGGCTCACACCTGTAATCTCAACACTTCAGGAGGCTGAGGCAGGCAGATCACTTGAGGTCA ACGGTGGCTCACACCTGTAATCTCAACACTTCGGGAGGCTGAGGCAGGCAGATCACTTGAGGTCA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1259710292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26829667 76053 RMVar_ID_76053 Human_SNP_ID_274809866 m1A Human chr6 + 42889245 42889245 42889245 GGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAATTCTGTCCCTAC GGCAGATCACTTGAGGTCAGGAGTTCGAGACCGGCCTGACCAACATGGAGAAATTCTGTCCCTAC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1134325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829858 76054 RMVar_ID_76054 Human_SNP_ID_274809878 m1A Human chr6 + 42889285 42889285 42889285 CAACATGGAGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTG CAACATGGAGAAATTCTGTCCCTACTGAAAATGCAAAATTAGCCGGATGTGGTGGTGCATGCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1134326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540170 76055 RMVar_ID_76055 Human_SNP_ID_274809906 m1A Human chr6 + 42889398 42889398 42889398 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCATTGCACTCCACCTTGGGCAACAAAAGCAA GGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCATTGCACTCCACCTTGGGCAACAAAAGCAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs3196534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18076790,Human_RBP_ID_22406625,Human_RBP_ID_23195646,Human_RBP_ID_26540171,Human_RBP_ID_27524829 76056 RMVar_ID_76056 Human_SNP_ID_274810283 m1A Human chr6 - 42890541 42890541 42890541 TCCGACCCTCAGGATAGGAACGGCCCCGGCGGAGCCTGGCTTGGTTGAGGCAGCGACTGCGCCTT TCCGACCCTCAGGATAGGAACGGCCCCGGCGGGGCCTGGCTTGGTTGAGGCAGCGACTGCGCCTT T C C6orf226 Ensembl:ENSG00000221821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42890494..42890586 26863196 MeRIP-seq:(Medium) rs780563854 Functional Loss SNV dbSNP153 33..33 33 - - - 76057 RMVar_ID_76057 Human_SNP_ID_274810412 m1A Human chr6 - 42890765 42890765 42890765 CGACCCGACATGGAGCGTCCCCGCAGTCCCCAATGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT CGACCCGACATGGAGCGTCCCCGCAGTCCCCATTGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT T A C6orf226 Ensembl:ENSG00000221821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42890671..42890793 26863196 MeRIP-seq:(Medium) rs370729479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4890228,Human_RBP_ID_5511728 Human_miRNA_ID_694383 76058 RMVar_ID_76058 Human_SNP_ID_274810413 m1A Human chr6 - 42890765 42890765 42890765 CGACCCGACATGGAGCGTCCCCGCAGTCCCCAATGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT CGACCCGACATGGAGCGTCCCCGCAGTCCCCAGTGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT T C C6orf226 Ensembl:ENSG00000221821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42890671..42890793 26863196 MeRIP-seq:(Medium) rs370729479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4890228,Human_RBP_ID_5511728 Human_miRNA_ID_694383 76059 RMVar_ID_76059 Human_SNP_ID_274810440 m1A Human chr6 - 42890795 42890795 42890795 TTCTCTGCATTACACGCCGGTCAGGATTCGCGACCCGACATGGAGCGTCCCCGCAGTCCCCAATG TTCTCTGCATTACACGCCGGTCAGGATTCGCGGCCCGACATGGAGCGTCCCCGCAGTCCCCAATG T C C6orf226 Ensembl:ENSG00000221821 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42890584..42890803 26863196 MeRIP-seq:(Medium) rs1382736076 Functional Loss SNV dbSNP153 33..33 33 - - - 76060 RMVar_ID_76060 Human_SNP_ID_274820501 m1A Human chr6 + 42928631 42928631 42928631 GATGAGAGTTTTACTGAGTATCTCCTTGTGCCAGGCACCCTGTTGTTGCTGGGGAAGCGGAAGGG GATGAGAGTTTTACTGAGTATCTCCTTGTGCCGGGCACCCTGTTGTTGCTGGGGAAGCGGAAGGG A G NONHSAG043795.2 RNACentral:URS00009AEC4D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42928385..42928634 26863196 MeRIP-seq:(Medium) rs1428852557 Functional Loss SNV dbSNP153 33..33 33 - - - 76061 RMVar_ID_76061 Human_SNP_ID_274820801 m1A Human chr6 - 42929543 42929543 42929543 TCCATGGCCCGGCCGGGCCCGGACCCTAAAGGACCGGGCGGTTCCTCCTCCCGCGGCGCGCGCGG TCCATGGCCCGGCCGGGCCCGGACCCTAAAGGGCCGGGCGGTTCCTCCTCCCGCGGCGCGCGCGG T C RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42929403..42934632 26863196 MeRIP-seq:(Medium) rs749701522 Functional Loss SNV dbSNP153 33..33 33 - - - 76062 RMVar_ID_76062 Human_SNP_ID_274820802 m1A Human chr6 - 42929543 42929543 42929543 TCCATGGCCCGGCCGGGCCCGGACCCTAAAGGACCGGGCGGTTCCTCCTCCCGCGGCGCGCGCGG TCCATGGCCCGGCCGGGCCCGGACCCTAAAGGCCCGGGCGGTTCCTCCTCCCGCGGCGCGCGCGG T G RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42929403..42934632 26863196 MeRIP-seq:(Medium) rs749701522 Functional Loss SNV dbSNP153 33..33 33 - - - 76063 RMVar_ID_76063 Human_SNP_ID_274822090 m1A Human chr6 - 42934542 42934542 42934542 GCCTTCTGGTCCAGGATGCCATAGCCCGTGCCAATCACCTCCTTGGTCTTGCCGGTTTCCTCAAA GCCTTCTGGTCCAGGATGCCATAGCCCGTGCCTATCACCTCCTTGGTCTTGCCGGTTTCCTCAAA T A RF00017-4590,RF00017-1033 RNACentral:URS0000965567,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:42929551..42934581 32194978 MeRIP-seq:(Medium) rs761244184 Functional Loss SNV dbSNP153 33..33 33 - - - 76064 RMVar_ID_76064 Human_SNP_ID_274823112 m1A Human chr6 + 42938604 42938604 42938604 CCTGGCAGAGCAGTGGTCCGGCAAGAAGGGAGACACAGCTGCCCTGGGAGGGAAGAAGTCCAAGA CCTGGCAGAGCAGTGGTCCGGCAAGAAGGGAGGCACAGCTGCCCTGGGAGGGAAGAAGTCCAAGA A G CNPY3 Ensembl:ENSG00000137161 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:42938193..42939150 32194978 MeRIP-seq:(Medium) rs140628883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664742,Human_RBP_ID_7607957,Human_RBP_ID_22461272 Human_Splice_Rec_770628 RMVar_hsa_circ_103832,RMVar_hsa_circ_80137,RMVar_hsa_circ_238497,RMVar_hsa_circ_238498 76065 RMVar_ID_76065 Human_SNP_ID_274823138 m1A Human chr6 + 42938669 42938669 42938669 AGAAGAGCAGCAGGGCCAAGGCAGCAGGCGGCAGGAGTAGCAGCAGCAAACAAAGGAAGGAGCTG AGAAGAGCAGCAGGGCCAAGGCAGCAGGCGGCGGGAGTAGCAGCAGCAAACAAAGGAAGGAGCTG A G CNPY3 Ensembl:ENSG00000137161 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42937747..42938800 26863196 MeRIP-seq:(Medium) rs1179843165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903327,Human_RBP_ID_17664101,Human_RBP_ID_22773611,Human_RBP_ID_26353972 RMVar_hsa_circ_103832,RMVar_hsa_circ_80137,RMVar_hsa_circ_238497,RMVar_hsa_circ_238498 76066 RMVar_ID_76066 Human_SNP_ID_274823140 m1A Human chr6 + 42938675 42938675 42938675 GCAGCAGGGCCAAGGCAGCAGGCGGCAGGAGTAGCAGCAGCAAACAAAGGAAGGAGCTGGGTGGC GCAGCAGGGCCAAGGCAGCAGGCGGCAGGAGTGGCAGCAGCAAACAAAGGAAGGAGCTGGGTGGC A G CNPY3 Ensembl:ENSG00000137161 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:42938651..42938675 32194978 MeRIP-seq:(Medium) rs746693743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903327,Human_RBP_ID_17664101,Human_RBP_ID_22773611,Human_RBP_ID_26353972 RMVar_hsa_circ_103832,RMVar_hsa_circ_80137,RMVar_hsa_circ_238497,RMVar_hsa_circ_238498 76067 RMVar_ID_76067 Human_SNP_ID_274823257 m1A Human chr6 + 42939095 42939095 42939095 CTCAGGAGGGGCAGGTGTCAGAACTGGGCACCAGGACTGGAGCCCCCTCCGGAGACCAAACTCAC CTCAGGAGGGGCAGGTGTCAGAACTGGGCACCGGGACTGGAGCCCCCTCCGGAGACCAAACTCAC A G CNPY3 Ensembl:ENSG00000137161 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:42938951..42939161 26863196 MeRIP-seq:(Medium) rs1326107320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5122497,Human_RBP_ID_17309904,Human_RBP_ID_17664105,Human_RBP_ID_27347423 Human_miRNA_ID_255604 RMVar_hsa_circ_103832,RMVar_hsa_circ_80137,RMVar_hsa_circ_238497,RMVar_hsa_circ_238498 76068 RMVar_ID_76068 Human_SNP_ID_274827665 m1A Human chr6 - 42956422 42956422 42956422 CCAAGAGGAATCAGAAACCTGAAGTTAGAAAGACTCGACGAGAACAAGCTATCAGGGCTGCTAAG CCAAGAGGAATCAGAAACCTGAAGTTAGAAAGGCTCGACGAGAACAAGCTATCAGGGCTGCTAAG T C RPL24P4 Ensembl:ENSG00000181524 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878940077 Functional Loss SNV dbSNP153 33..33 33 - - - 76069 RMVar_ID_76069 Human_SNP_ID_274834299 m1A Human chr6 - 42978539 42978539 42978539 CTCCAGGGAGTTCTGGGAGGGACTGGAGATTCACTAGGGGTGAGCCGGAGCTGTCTCCGTGGCCT CTCCAGGGAGTTCTGGGAGGGACTGGAGATTCGCTAGGGGTGAGCCGGAGCTGTCTCCGTGGCCT T C PEX6 Ensembl:ENSG00000124587 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42978489..42978729 26863196 MeRIP-seq:(Medium) rs886043877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790140,Human_RBP_ID_841154,Human_RBP_ID_7608065,Human_RBP_ID_9336673,Human_RBP_ID_22106439,Human_RBP_ID_22482346 RMVar_hsa_circ_102668,RMVar_hsa_circ_98476,RMVar_hsa_circ_238514,RMVar_hsa_circ_238516 76070 RMVar_ID_76070 Human_SNP_ID_274834300 m1A Human chr6 - 42978539 42978539 42978539 CTCCAGGGAGTTCTGGGAGGGACTGGAGATTCACTAGGGGTGAGCCGGAGCTGTCTCCGTGGCCT CTCCAGGGAGTTCTGGGAGGGACTGGAGATTCCCTAGGGGTGAGCCGGAGCTGTCTCCGTGGCCT T G PEX6 Ensembl:ENSG00000124587 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:42978489..42978729 26863196 MeRIP-seq:(Medium) rs886043877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790140,Human_RBP_ID_841154,Human_RBP_ID_7608065,Human_RBP_ID_9336673,Human_RBP_ID_22106439,Human_RBP_ID_22482346 RMVar_hsa_circ_102668,RMVar_hsa_circ_98476,RMVar_hsa_circ_238514,RMVar_hsa_circ_238516 76071 RMVar_ID_76071 Human_SNP_ID_274834342 m1A Human chr6 + 42978650 42978649 42978651 GGTGGGGGCCGACTGCTGTCCCCAGACTCTGGACACAGTCTGGCCCGCCCGCGGAGCTCAGTCAC GGTGGGGGCCGACTGCTGTCCCCAGACTCTGG__ACAGTCTGGCCCGCCCGCGGAGCTCAGTCAC GAC G RF00017-4567 RNACentral:URS000093B3AD SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42978356..42978784 26863196 MeRIP-seq:(Medium) rs61753223 Functional Loss DEL dbSNP153 33..34 33 - - - 76072 RMVar_ID_76072 Human_SNP_ID_274834358 m1A Human chr6 + 42978677 42978677 42978677 TCTGGACACAGTCTGGCCCGCCCGCGGAGCTCAGTCACAGCCAGCCGAGTCCCTGGGCCCAGCAG TCTGGACACAGTCTGGCCCGCCCGCGGAGCTCCGTCACAGCCAGCCGAGTCCCTGGGCCCAGCAG A C RF00017-4567 RNACentral:URS000093B3AD SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:42978626..42978825 32194978 MeRIP-seq:(Medium) rs1257237341 Functional Loss SNV dbSNP153 33..33 33 - - - 76073 RMVar_ID_76073 Human_SNP_ID_274834363 m1A Human chr6 + 42978683 42978683 42978683 CACAGTCTGGCCCGCCCGCGGAGCTCAGTCACAGCCAGCCGAGTCCCTGGGCCCAGCAGCCCTTG CACAGTCTGGCCCGCCCGCGGAGCTCAGTCACGGCCAGCCGAGTCCCTGGGCCCAGCAGCCCTTG A G RF00017-4567 RNACentral:URS000093B3AD SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:42978576..42978750 26863196 MeRIP-seq:(Medium) rs1254015920 Functional Loss SNV dbSNP153 33..33 33 - - - 76074 RMVar_ID_76074 Human_SNP_ID_274836153 m1A Human chr6 + 42984637 42984633 42984638 GGCCGAGTGCGGCCGAGCAAAGCCGGAGCCGGAGCGGGGCCGCAGGAGACGGGCCGGGTCCGGAC GGCCGAGTGCGGCCGAGCAAAGCCGGAGC_____CGGGGCCGCAGGAGACGGGCCGGGTCCGGAC CCGGAG C PPP2R5D Ensembl:ENSG00000112640 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:42984551..43006603 26863196 MeRIP-seq:(Medium) rs768738918 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_790825,Human_RBP_ID_4903328,Human_RBP_ID_18425435 Human_Splice_Rec_770707,Human_Splice_Rec_770735,Human_Splice_Rec_770765,Human_Splice_Rec_770795,Human_Splice_Rec_770825 76075 RMVar_ID_76075 Human_SNP_ID_274836200 m1A Human chr6 + 42984702 42984699 42984702 GGGCCGAGATGCCCTATAAACTGAAAAAGGAGAAGGTGAGCGTGGCCCTTTTTCCCCCACCGCCG GGGCCGAGATGCCCTATAAACTGAAAAAGG___AGGTGAGCGTGGCCCTTTTTCCCCCACCGCCG GAGA G PPP2R5D Ensembl:ENSG00000112640 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:42984651..42984725;chr6:42984576..42984784 26863196 MeRIP-seq:(Medium) rs768198586 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4904037,Human_RBP_ID_19131124 Human_Splice_Rec_770707,Human_Splice_Rec_770735,Human_Splice_Rec_770765,Human_Splice_Rec_770795,Human_Splice_Rec_770825 76076 RMVar_ID_76076 Human_SNP_ID_274841876 m1A Human chr6 + 43007243 43007243 43007243 TTCCGGACGCTGCCACCTTCATCGAATCCCACAGGGGCTGAGTTTGACCCAGAGGAAGATGAGCC TTCCGGACGCTGCCACCTTCATCGAATCCCACGGGGGCTGAGTTTGACCCAGAGGAAGATGAGCC A G PPP2R5D Ensembl:ENSG00000112640 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43007176..43007275 32194978 MeRIP-seq:(Medium) rs947797301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4890396,Human_RBP_ID_8901547,Human_RBP_ID_18076860,Human_RBP_ID_24163659 Human_Splice_Rec_770712,Human_Splice_Rec_770713,Human_Splice_Rec_770742,Human_Splice_Rec_770743,Human_Splice_Rec_770772,Human_Splice_Rec_770773,Human_Splice_Rec_770802,Human_Splice_Rec_770803,Human_Splice_Rec_770828,Human_Splice_Rec_770829,Human_Splice_Rec_770854,Human_Splice_Rec_770855,Human_Splice_Rec_770876,Human_Splice_Rec_770877 Human_miRNA_ID_937595,Human_miRNA_ID_957748,Human_miRNA_ID_961221 RMVar_hsa_circ_114799,RMVar_hsa_circ_110308,RMVar_hsa_circ_238517,RMVar_hsa_circ_238518 76077 RMVar_ID_76077 Human_SNP_ID_274842795 m1A Human chr6 - 43010909 43010909 43010909 GGGTCTCTGTCTCCATCGAGTACACAGGGGGCAGTGGTGGAGGGGCTCGGAACATGGGATACTGA GGGTCTCTGTCTCCATCGAGTACACAGGGGGCGGTGGTGGAGGGGCTCGGAACATGGGATACTGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43010876..43010950 32194978 MeRIP-seq:(Medium) rs767659728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18076867 76078 RMVar_ID_76078 Human_SNP_ID_274842962 m1A Human chr6 - 43011427 43011427 43011427 AAGAGGGACCATTCTGTGGGTGTCCCTGCTTCAAGTGCCCACATCCCCCTCCCTTGAGTAGCTAG AAGAGGGACCATTCTGTGGGTGTCCCTGCTTCGAGTGCCCACATCCCCCTCCCTTGAGTAGCTAG T C MEA1 Ensembl:ENSG00000124733 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43011376..43011450 32194978 MeRIP-seq:(Medium) rs1203719673 Functional Loss SNV dbSNP153 33..33 33 - - - 76079 RMVar_ID_76079 Human_SNP_ID_274843179 m1A Human chr6 - 43012337 43012337 43012337 CCCTTTCCACATCAAGGCACATCAGACTTCTCAGAGACCCACTTTATTCAGTTCTGTACATATGG CCCTTTCCACATCAAGGCACATCAGACTTCTCGGAGACCCACTTTATTCAGTTCTGTACATATGG T C MEA1 Ensembl:ENSG00000124733 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43012287..43012539 26863196 MeRIP-seq:(Medium) rs1254192285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664831,Human_RBP_ID_1673569,Human_RBP_ID_2021559,Human_RBP_ID_7608165,Human_RBP_ID_17308979,Human_RBP_ID_17420244,Human_RBP_ID_17664109,Human_RBP_ID_18076893,Human_RBP_ID_18958420,Human_RBP_ID_21902395,Human_RBP_ID_23062237 Human_miRNA_ID_1795381 76080 RMVar_ID_76080 Human_SNP_ID_274843402 m1A Human chr6 - 43013006 43013006 43013006 GGCTCTGCAGGCCCTGGGGCTTCATTTGCCAGACCCACCATTAGAGAGTGAAGATGAAGATGAGG GGCTCTGCAGGCCCTGGGGCTTCATTTGCCAGGCCCACCATTAGAGAGTGAAGATGAAGATGAGG T C MEA1 Ensembl:ENSG00000124733 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43012926..43013050 32194978 MeRIP-seq:(Medium) rs1266540406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1047737,Human_RBP_ID_2021565,Human_RBP_ID_5327458,Human_RBP_ID_9194735,Human_RBP_ID_9400554,Human_RBP_ID_17663311,Human_RBP_ID_18076900,Human_RBP_ID_22105136 Human_Splice_Rec_770898,Human_Splice_Rec_770899,Human_Splice_Rec_770904,Human_Splice_Rec_770905,Human_Splice_Rec_770910,Human_Splice_Rec_770911,Human_Splice_Rec_770916,Human_Splice_Rec_770917,Human_Splice_Rec_770922,Human_Splice_Rec_770923,Human_Splice_Rec_770928,Human_Splice_Rec_770929 RMVar_hsa_circ_346184 76081 RMVar_ID_76081 Human_SNP_ID_274843514 m1A Human chr6 - 43013299 43013299 43013299 CTTCCCCAATCAGACTGAGGAACTGGGACATCAGGGCCCTTCAGAAGGCACTGGGGATTGGAGCA CTTCCCCAATCAGACTGAGGAACTGGGACATCGGGGCCCTTCAGAAGGCACTGGGGATTGGAGCA T C MEA1 Ensembl:ENSG00000124733 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:43013251..43013400 26863196 MeRIP-seq:(Medium) rs763536971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1673577,Human_RBP_ID_2021569,Human_RBP_ID_4890507,Human_RBP_ID_5122003,Human_RBP_ID_7608179,Human_RBP_ID_8645518,Human_RBP_ID_8901563,Human_RBP_ID_9400556,Human_RBP_ID_15830702,Human_RBP_ID_18076902 Human_Splice_Rec_770902,Human_Splice_Rec_770908,Human_Splice_Rec_770914,Human_Splice_Rec_770920,Human_Splice_Rec_770926 RMVar_hsa_circ_238521,RMVar_hsa_circ_346184,RMVar_hsa_circ_376870 76082 RMVar_ID_76082 Human_SNP_ID_274843542 m1A Human chr6 - 43013355 43013353 43013356 CCTGCCCGGATGGCAACAGTAGTTCTAGGAGGAGACACCATGGGCCCTGAGCGTATCTTCCCCAA CCTGCCCGGATGGCAACAGTAGTTCTAGGAG___ACACCATGGGCCCTGAGCGTATCTTCCCCAA TCTC T MEA1 Ensembl:ENSG00000124733 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43013126..43013400 26863196 MeRIP-seq:(Medium) rs749948541 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_664843,Human_RBP_ID_792113,Human_RBP_ID_1673578,Human_RBP_ID_2021571,Human_RBP_ID_4903329,Human_RBP_ID_5152186,Human_RBP_ID_7608182,Human_RBP_ID_9400556,Human_RBP_ID_15830705,Human_RBP_ID_17536320,Human_RBP_ID_26355181 Human_Splice_Rec_770902,Human_Splice_Rec_770908,Human_Splice_Rec_770914,Human_Splice_Rec_770920,Human_Splice_Rec_770926 Human_miRNA_ID_2353133,Human_miRNA_ID_2572652,Human_miRNA_ID_2909161 RMVar_hsa_circ_238521,RMVar_hsa_circ_346184,RMVar_hsa_circ_376870 76083 RMVar_ID_76083 Human_SNP_ID_274844635 m1A Human chr6 - 43017182 43017182 43017182 GGTGCACTGTCCACCGTAACATCCCCTGGGCCACTGGTTACAGCAACATGCCCCCCCGGCACGGC GGTGCACTGTCCACCGTAACATCCCCTGGGCCGCTGGTTACAGCAACATGCCCCCCCGGCACGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:43017072..43017253 26863196 MeRIP-seq:(Medium) rs1400401790 Functional Loss SNV dbSNP153 33..33 33 - - - 76084 RMVar_ID_76084 Human_SNP_ID_274845581 m1A Human chr6 - 43020757 43020757 43020757 GCAGGGGCAGTGAAGATGACAGCAGGCTCAGGAGGGGAGGTGGCAGAAACTTCCTCCTACCCATG GCAGGGGCAGTGAAGATGACAGCAGGCTCAGGGGGGGAGGTGGCAGAAACTTCCTCCTACCCATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43020708..43021165 26863196 MeRIP-seq:(Medium) rs754573243 Functional Loss SNV dbSNP153 33..33 33 - - - 76085 RMVar_ID_76085 Human_SNP_ID_274845596 m1A Human chr6 + 43020792 43020792 43020792 TGAGCCTGCTGTCATCTTCACTGCCCCTGCCCATCTGTCACCCACCTGCTCCTTTGACCCCTGGA TGAGCCTGCTGTCATCTTCACTGCCCCTGCCCGTCTGTCACCCACCTGCTCCTTTGACCCCTGGA A G KLHDC3 Ensembl:ENSG00000124702 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:43020751..43020800 26863196 MeRIP-seq:(Medium) rs902324856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664876,Human_RBP_ID_792111,Human_RBP_ID_17663753,Human_RBP_ID_18076919,Human_RBP_ID_26828535 76086 RMVar_ID_76086 Human_SNP_ID_274845737 m1A Human chr6 - 43021167 43021167 43021167 CCACCTCCCCAAGACGGGGAGAAGGAGGTCTCATGCCAACAGCTGCAACTCCTTTCAGCTCCCAG CCACCTCCCCAAGACGGGGAGAAGGAGGTCTCCTGCCAACAGCTGCAACTCCTTTCAGCTCCCAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43020776..43021225 32194978 MeRIP-seq:(Medium) rs1265260619 Functional Loss SNV dbSNP153 33..33 33 - - - 76087 RMVar_ID_76087 Human_SNP_ID_274845979 m1A Human chr6 - 43021764 43021686 43021764 CCATGCCCTCACCCCTCAATAGGTCGCGGGCCACGGCCGCGGGCTCCAGGCCCCCGCCGTCCTCC CCATGCCCTCACCCCTCAATAGGTCGCGGGCC_________________________________ GGGCCGGGGCCGGGGCCCGACGTCCCCGCGGGGCCCGGGACCGCGAGGAGGACGGCGGGGGCCTGGAGCCCGCGGCCGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr6:43021626..43021814;chr6:43021677..43021771 26863196,26863410 MeRIP-seq:(Medium) rs1561861291 Functional Loss DEL dbSNP153 33..65 33 - - - 76088 RMVar_ID_76088 Human_SNP_ID_274845987 m1A Human chr6 + 43021725 43021694 43021725 GGCCGGGGCCCGACGTCCCCGCGGGGCCCGGGACCGCGAGGAGGACGGCGGGGGCCTGGAGCCCG GG_______________________________CCGCGAGGAGGACGGCGGGGGCCTGGAGCCCG GCCGGGGCCCGACGTCCCCGCGGGGCCCGGGA G RRP36 Ensembl:ENSG00000124541 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:43021626..43021800 26863410 MeRIP-seq:(Medium) rs995132612 Functional Loss DEL dbSNP153 3..33 33 - - - Human_RBP_ID_4890593 Human_Splice_Rec_770989 RMVar_hsa_circ_84723,RMVar_hsa_circ_238523 76089 RMVar_ID_76089 Human_SNP_ID_274845998 m1A Human chr6 + 43021725 43021700 43021725 GGCCGGGGCCCGACGTCCCCGCGGGGCCCGGGACCGCGAGGAGGACGGCGGGGGCCTGGAGCCCG GGCCGGGG_________________________CCGCGAGGAGGACGGCGGGGGCCTGGAGCCCG GCCCGACGTCCCCGCGGGGCCCGGGA G RRP36 Ensembl:ENSG00000124541 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:43021626..43021800 26863410 MeRIP-seq:(Medium) rs1026568887 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_4890593 Human_Splice_Rec_770989 RMVar_hsa_circ_84723,RMVar_hsa_circ_238523 76090 RMVar_ID_76090 Human_SNP_ID_274846022 m1A Human chr6 - 43021764 43021764 43021764 CCATGCCCTCACCCCTCAATAGGTCGCGGGCCACGGCCGCGGGCTCCAGGCCCCCGCCGTCCTCC CCATGCCCTCACCCCTCAATAGGTCGCGGGCCGCGGCCGCGGGCTCCAGGCCCCCGCCGTCCTCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr6:43021626..43021814;chr6:43021677..43021771 26863196,26863410 MeRIP-seq:(Medium) rs540615157 Functional Loss SNV dbSNP153 33..33 33 - - - 76091 RMVar_ID_76091 Human_SNP_ID_274846023 m1A Human chr6 - 43021764 43021764 43021764 CCATGCCCTCACCCCTCAATAGGTCGCGGGCCACGGCCGCGGGCTCCAGGCCCCCGCCGTCCTCC CCATGCCCTCACCCCTCAATAGGTCGCGGGCCCCGGCCGCGGGCTCCAGGCCCCCGCCGTCCTCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr6:43021626..43021814;chr6:43021677..43021771 26863196,26863410 MeRIP-seq:(Medium) rs540615157 Functional Loss SNV dbSNP153 33..33 33 - - - 76092 RMVar_ID_76092 Human_SNP_ID_274847701 m1A Human chr6 + 43027264 43027261 43027264 CAGCAACTGCTTCAGCGAATGGTGAGTGGGTAATAATTGTGGTGGGTAATGAAAGCAATTAAAGG CAGCAACTGCTTCAGCGAATGGTGAGTGGG___TAATTGTGGTGGGTAATGAAAGCAATTAAAGG GTAA G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43027261..43027374 26863196 MeRIP-seq:(Medium) rs757698090 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5398228,Human_RBP_ID_22105958 Human_Splice_Rec_770996 RMVar_hsa_circ_84723,RMVar_hsa_circ_238523,RMVar_hsa_circ_301306,RMVar_hsa_circ_127718,RMVar_hsa_circ_118349,RMVar_hsa_circ_238525,RMVar_hsa_circ_238526,RMVar_hsa_circ_238527,RMVar_hsa_circ_78782,RMVar_hsa_circ_357666,RMVar_hsa_circ_118693,RMVar_hsa_circ_238528,RMVar_hsa_circ_238529 76093 RMVar_ID_76093 Human_SNP_ID_274848609 m1A Human chr6 + 43029809 43029809 43029809 CAGCTAATTTCTTTCGTATTTTTAGTAGAGATAGAGTTTTGCCATGTTGGCTAGTTTGATCTTAA CAGCTAATTTCTTTCGTATTTTTAGTAGAGATGGAGTTTTGCCATGTTGGCTAGTTTGATCTTAA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs887769570 Functional Loss SNV dbSNP153 33..33 33 - - - 76094 RMVar_ID_76094 Human_SNP_ID_274851188 m1A Human chr6 - 43038900 43038900 43038900 GCTGGGCTGGGCTGAGCTGCAGTTTGGGAACCAGACCCTGCATGTGTCCACCGTGCAGATGTGGC GCTGGGCTGGGCTGAGCTGCAGTTTGGGAACCGGACCCTGCATGTGTCCACCGTGCAGATGTGGC T C CUL7 Ensembl:ENSG00000044090 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43038851..43038975 32194978 MeRIP-seq:(Medium) rs1167055934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9309314,Human_RBP_ID_18472092 Human_Splice_Rec_771050,Human_Splice_Rec_771051,Human_Splice_Rec_771100,Human_Splice_Rec_771101,Human_Splice_Rec_771140,Human_Splice_Rec_771141,Human_Splice_Rec_771190,Human_Splice_Rec_771191,Human_Splice_Rec_771240,Human_Splice_Rec_771241,Human_Splice_Rec_771276,Human_Splice_Rec_771277,Human_Splice_Rec_771324,Human_Splice_Rec_771325 RMVar_hsa_circ_79942,RMVar_hsa_circ_126723,RMVar_hsa_circ_238533,RMVar_hsa_circ_76231,RMVar_hsa_circ_238532,RMVar_hsa_circ_107299,RMVar_hsa_circ_127468,RMVar_hsa_circ_238536,RMVar_hsa_circ_238538,RMVar_hsa_circ_84568,RMVar_hsa_circ_238539,RMVar_hsa_circ_238537 76095 RMVar_ID_76095 Human_SNP_ID_274851640 m1A Human chr6 - 43040401 43040401 43040401 CCTTCAGGTGGGCCTTGGGGCCAGTGGCAAGGAGCACAAGAGCGAGAAGGAAGAGGAAGCTGGGG CCTTCAGGTGGGCCTTGGGGCCAGTGGCAAGGGGCACAAGAGCGAGAAGGAAGAGGAAGCTGGGG T C CUL7 Ensembl:ENSG00000044090 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43040351..43040450 32194978 MeRIP-seq:(Medium) rs760350095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840486,Human_RBP_ID_5532436,Human_RBP_ID_19018578,Human_RBP_ID_26355183 Human_Splice_Rec_771048,Human_Splice_Rec_771098,Human_Splice_Rec_771138,Human_Splice_Rec_771188,Human_Splice_Rec_771238,Human_Splice_Rec_771274,Human_Splice_Rec_771322 RMVar_hsa_circ_20882,RMVar_hsa_circ_79942,RMVar_hsa_circ_126723,RMVar_hsa_circ_238533,RMVar_hsa_circ_76231,RMVar_hsa_circ_238532,RMVar_hsa_circ_107299,RMVar_hsa_circ_127468,RMVar_hsa_circ_238536,RMVar_hsa_circ_238538,RMVar_hsa_circ_84568,RMVar_hsa_circ_238539,RMVar_hsa_circ_238537 76096 RMVar_ID_76096 Human_SNP_ID_274851641 m1A Human chr6 - 43040405 43040402 43040405 TGCTCCTTCAGGTGGGCCTTGGGGCCAGTGGCAAGGAGCACAAGAGCGAGAAGGAAGAGGAAGCT TGCTCCTTCAGGTGGGCCTTGGGGCCAGTGGC___GAGCACAAGAGCGAGAAGGAAGAGGAAGCT CCTT C CUL7 Ensembl:ENSG00000044090 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43040267..43040437 26863196 MeRIP-seq:(Medium) rs1227943566 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_840486,Human_RBP_ID_5532436,Human_RBP_ID_19018578,Human_RBP_ID_26355183 Human_Splice_Rec_771048,Human_Splice_Rec_771098,Human_Splice_Rec_771138,Human_Splice_Rec_771188,Human_Splice_Rec_771238,Human_Splice_Rec_771274,Human_Splice_Rec_771322 RMVar_hsa_circ_20882,RMVar_hsa_circ_79942,RMVar_hsa_circ_126723,RMVar_hsa_circ_238533,RMVar_hsa_circ_76231,RMVar_hsa_circ_238532,RMVar_hsa_circ_107299,RMVar_hsa_circ_127468,RMVar_hsa_circ_238536,RMVar_hsa_circ_238538,RMVar_hsa_circ_84568,RMVar_hsa_circ_238539,RMVar_hsa_circ_238537 76097 RMVar_ID_76097 Human_SNP_ID_274851746 m1A Human chr6 + 43040670 43040670 43040670 CAACATCTGCTGGGGGAGGCGGTTGGGGAAGCAGGGACCGATCTGCTCCAGCACGGCCCCCTCCA CAACATCTGCTGGGGGAGGCGGTTGGGGAAGCGGGGACCGATCTGCTCCAGCACGGCCCCCTCCA A G RF00017-3341 RNACentral:URS000091B6F5 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43040526..43040725 32194978 MeRIP-seq:(Medium) rs1181294891 Functional Loss SNV dbSNP153 33..33 33 - - - 76098 RMVar_ID_76098 Human_SNP_ID_274852526 m1A Human chr6 + 43043157 43043155 43043157 GCTTGGAAGGCCCCGGGTAGCCAAGGAGCTCCAGTCGTGGCTTCTGTTTCTGCCTTCTGTAGAGA GCTTGGAAGGCCCCGGGTAGCCAAGGAGCTC__GTCGTGGCTTCTGTTTCTGCCTTCTGTAGAGA CCA C KLC4 Ensembl:ENSG00000137171 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43043107..43043257 32194978 MeRIP-seq:(Medium) rs730880262 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_771344 Clinvar_Rec_348 76099 RMVar_ID_76099 Human_SNP_ID_274854999 m1A Human chr6 + 43051022 43051022 43051022 TTGCTCTGCCGAAACTCGCCCTCATCCCCGGCACTGATCTCCTCATAATCATCCAGCATCCGCAC TTGCTCTGCCGAAACTCGCCCTCATCCCCGGCGCTGATCTCCTCATAATCATCCAGCATCCGCAC A G KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43050951..43051071 26863196 MeRIP-seq:(Medium) rs1193312893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18866121 76100 RMVar_ID_76100 Human_SNP_ID_274855919 m1A Human chr6 + 43053723 43053723 43053723 GGCGGCGACTTGGGCCCCACCTGGGCCCCGCGAGGGGGTCGAGACGGAGAGACGGGAGGGGGCGT GGCGGCGACTTGGGCCCCACCTGGGCCCCGCGCGGGGGTCGAGACGGAGAGACGGGAGGGGGCGT A C KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43053675..43053842 26863196 MeRIP-seq:(Medium) rs547052216 Functional Loss SNV dbSNP153 33..33 33 - - - 76101 RMVar_ID_76101 Human_SNP_ID_274856263 m1A Human chr6 - 43054336 43054336 43054336 GGCACCGCAAGGGGGGCTGGGCTGGCCGAAAGATTCGGCCACTACCCCCCATGAAGAGTTACGTG GGCACCGCAAGGGGGGCTGGGCTGGCCGAAAGTTTCGGCCACTACCCCCCATGAAGAGTTACGTG T A AL355385.2,MRPL2 Ensembl:ENSG00000288564,Ensembl:ENSG00000112651 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43054286..43054448 26863196 MeRIP-seq:(Medium) rs749144020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1047773,Human_RBP_ID_4890725,Human_RBP_ID_17663138,Human_RBP_ID_18076970,Human_RBP_ID_22462072,Human_RBP_ID_27347505 76102 RMVar_ID_76102 Human_SNP_ID_274856264 m1A Human chr6 - 43054336 43054336 43054336 GGCACCGCAAGGGGGGCTGGGCTGGCCGAAAGATTCGGCCACTACCCCCCATGAAGAGTTACGTG GGCACCGCAAGGGGGGCTGGGCTGGCCGAAAGCTTCGGCCACTACCCCCCATGAAGAGTTACGTG T G AL355385.2,MRPL2 Ensembl:ENSG00000288564,Ensembl:ENSG00000112651 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43054286..43054448 26863196 MeRIP-seq:(Medium) rs749144020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1047773,Human_RBP_ID_4890725,Human_RBP_ID_17663138,Human_RBP_ID_18076970,Human_RBP_ID_22462072,Human_RBP_ID_27347505 76103 RMVar_ID_76103 Human_SNP_ID_274856268 m1A Human chr6 - 43054340 43054340 43054340 CGGTGGCACCGCAAGGGGGGCTGGGCTGGCCGAAAGATTCGGCCACTACCCCCCATGAAGAGTTA CGGTGGCACCGCAAGGGGGGCTGGGCTGGCCGGAAGATTCGGCCACTACCCCCCATGAAGAGTTA T C AL355385.2,MRPL2 Ensembl:ENSG00000288564,Ensembl:ENSG00000112651 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43054294..43054414 26863196 MeRIP-seq:(Medium) rs1442119950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17663138,Human_RBP_ID_18076970 76104 RMVar_ID_76104 Human_SNP_ID_274856323 m1A Human chr6 - 43054446 43054446 43054446 AACGTGCGTAGCAACAGTAGGCCGAGTATCCAACGTTGATCATAACAAACGGGTCATTGGCAAGG AACGTGCGTAGCAACAGTAGGCCGAGTATCCAGCGTTGATCATAACAAACGGGTCATTGGCAAGG T C AL355385.2,MRPL2 Ensembl:ENSG00000288564,Ensembl:ENSG00000112651 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43054396..43054528 26863196 MeRIP-seq:(Medium) rs774510424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792036,Human_RBP_ID_1673639,Human_RBP_ID_15831171,Human_RBP_ID_18171477,Human_RBP_ID_22462754 Human_Splice_Rec_771604,Human_Splice_Rec_771618,Human_Splice_Rec_771620,Human_Splice_Rec_771628,Human_Splice_Rec_771632 76105 RMVar_ID_76105 Human_SNP_ID_274856964 m1A Human chr6 + 43056439 43056439 43056439 GCTTGTGGCCCCCGCCAATACCATGCACCCGGATTCGGCCTGTGGTTTAGGACAGTTGGGGGATA GCTTGTGGCCCCCGCCAATACCATGCACCCGGGTTCGGCCTGTGGTTTAGGACAGTTGGGGGATA A G KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:43056390..43057616 26863410 MeRIP-seq:(Medium) rs764512127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7608394,Human_RBP_ID_15831221 76106 RMVar_ID_76106 Human_SNP_ID_274857677 m1A Human chr6 + 43059313 43059287 43059314 ATTACCTGGGCGGCGGGGAACAGACTCGGGGCAGGGGCGGCGACGGTCGGGGGCGCCAGGTTCAG ATTACCT___________________________GGGCGGCGACGGTCGGGGGCGCCAGGTTCAG TGGGCGGCGGGGAACAGACTCGGGGCAG T KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,untreat control;HTR8/Svneo,Hypoxia IP chr6:43059291..43059378;chr6:43059307..43059408 26863410,32194978 MeRIP-seq:(Medium) rs1412513894 Functional Loss DEL dbSNP153 8..34 33 - - - RMVar_hsa_circ_5986 76107 RMVar_ID_76107 Human_SNP_ID_274857686 m1A Human chr6 + 43059313 43059312 43059313 ATTACCTGGGCGGCGGGGAACAGACTCGGGGCAGGGGCGGCGACGGTCGGGGGCGCCAGGTTCAG ATTACCTGGGCGGCGGGGAACAGACTCGGGGC_GGGGCGGCGACGGTCGGGGGCGCCAGGTTCAG CA C KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,untreat control;HTR8/Svneo,Hypoxia IP chr6:43059291..43059378;chr6:43059307..43059408 26863410,32194978 MeRIP-seq:(Medium) rs1561907993 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_5986 76108 RMVar_ID_76108 Human_SNP_ID_274857692 m1A Human chr6 + 43059323 43059323 43059323 CGGCGGGGAACAGACTCGGGGCAGGGGCGGCGACGGTCGGGGGCGCCAGGTTCAGAGAGCGCAGA CGGCGGGGAACAGACTCGGGGCAGGGGCGGCGGCGGTCGGGGGCGCCAGGTTCAGAGAGCGCAGA A G KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:43059293..43059380 26863410 MeRIP-seq:(Medium) rs768363057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5986 76109 RMVar_ID_76109 Human_SNP_ID_274857717 m1A Human chr6 - 43059363 43059363 43059363 AGGGTGTCGTGCTGATGGCCCTGTGCGCACTGACCCGCGCTCTGCGCTCTCTGAACCTGGCGCCC AGGGTGTCGTGCTGATGGCCCTGTGCGCACTGTCCCGCGCTCTGCGCTCTCTGAACCTGGCGCCC T A MRPL2 Ensembl:ENSG00000112651 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:43059249..43059425;chr6:43059210..43059425;chr6:43059229..43059425;chr6:43059252..43059450;chr6:43059228..43059425;chr6:43059235..43059425 26863196 MeRIP-seq:(Medium) rs374274657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664961,Human_RBP_ID_789480,Human_RBP_ID_1327655,Human_RBP_ID_1673644,Human_RBP_ID_4904049,Human_RBP_ID_5122271,Human_RBP_ID_5451278,Human_RBP_ID_5478222,Human_RBP_ID_9309338,Human_RBP_ID_9336172,Human_RBP_ID_15831266,Human_RBP_ID_22106442,Human_RBP_ID_24163781,Human_RBP_ID_26828542 Human_Splice_Rec_771609,Human_Splice_Rec_771621,Human_Splice_Rec_771629,Human_Splice_Rec_771633,Human_Splice_Rec_771639,Human_Splice_Rec_771643,Human_Splice_Rec_771651 Human_miRNA_ID_2249977 RMVar_hsa_circ_238553,RMVar_hsa_circ_89948,RMVar_hsa_circ_85944,RMVar_hsa_circ_238557 76110 RMVar_ID_76110 Human_SNP_ID_274857718 m1A Human chr6 - 43059363 43059363 43059363 AGGGTGTCGTGCTGATGGCCCTGTGCGCACTGACCCGCGCTCTGCGCTCTCTGAACCTGGCGCCC AGGGTGTCGTGCTGATGGCCCTGTGCGCACTGGCCCGCGCTCTGCGCTCTCTGAACCTGGCGCCC T C MRPL2 Ensembl:ENSG00000112651 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:43059249..43059425;chr6:43059210..43059425;chr6:43059229..43059425;chr6:43059252..43059450;chr6:43059228..43059425;chr6:43059235..43059425 26863196 MeRIP-seq:(Medium) rs374274657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664961,Human_RBP_ID_789480,Human_RBP_ID_1327655,Human_RBP_ID_1673644,Human_RBP_ID_4904049,Human_RBP_ID_5122271,Human_RBP_ID_5451278,Human_RBP_ID_5478222,Human_RBP_ID_9309338,Human_RBP_ID_9336172,Human_RBP_ID_15831266,Human_RBP_ID_22106442,Human_RBP_ID_24163781,Human_RBP_ID_26828542 Human_Splice_Rec_771609,Human_Splice_Rec_771621,Human_Splice_Rec_771629,Human_Splice_Rec_771633,Human_Splice_Rec_771639,Human_Splice_Rec_771643,Human_Splice_Rec_771651 Human_miRNA_ID_2249977 RMVar_hsa_circ_238553,RMVar_hsa_circ_89948,RMVar_hsa_circ_85944,RMVar_hsa_circ_238557 76111 RMVar_ID_76111 Human_SNP_ID_274858088 m1A Human chr6 + 43060449 43060449 43060449 GAGGGTGTTTGTCCTGGGTGGGGCTCTGGGCCAGGTCCTCTGGGTAGCTGTGAAGTGGTGAAAGA GAGGGTGTTTGTCCTGGGTGGGGCTCTGGGCCCGGTCCTCTGGGTAGCTGTGAAGTGGTGAAAGA A C KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43060445..43060654 26863196 MeRIP-seq:(Medium) rs1038373965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267321,Human_RBP_ID_8216076,Human_RBP_ID_9438152,Human_RBP_ID_18465576,Human_RBP_ID_22105141 RMVar_hsa_circ_5986 76112 RMVar_ID_76112 Human_SNP_ID_274858099 m1A Human chr6 - 43060496 43060496 43060496 GAGGATCTGCCCTGCCCAAAGTCCAGAAGTCCAGCGTTCCCACCCCTTCTTTCACCACTTCACAG GAGGATCTGCCCTGCCCAAAGTCCAGAAGTCCGGCGTTCCCACCCCTTCTTTCACCACTTCACAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43060485..43060568 26863196 MeRIP-seq:(Medium) rs1480019067 Functional Loss SNV dbSNP153 33..33 33 - - - 76113 RMVar_ID_76113 Human_SNP_ID_274858293 m1A Human chr6 + 43061394 43061394 43061394 GGATGAGCCTGCAGGCCACCGGCTCAGCCAAGAGGAGATCCTGGGGAGCACACGGCTGGTCAGCC GGATGAGCCTGCAGGCCACCGGCTCAGCCAAGGGGAGATCCTGGGGAGCACACGGCTGGTCAGCC A G KLC4 Ensembl:ENSG00000137171 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43061343..43061440 26863196 MeRIP-seq:(Medium) rs1219277414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252229,Human_RBP_ID_4904886,Human_RBP_ID_18425650,Human_RBP_ID_19018591,Human_RBP_ID_23067359,Human_RBP_ID_26353190 Human_Splice_Rec_771350,Human_Splice_Rec_771378,Human_Splice_Rec_771406,Human_Splice_Rec_771442,Human_Splice_Rec_771452,Human_Splice_Rec_771462,Human_Splice_Rec_771492,Human_Splice_Rec_771494,Human_Splice_Rec_771524,Human_Splice_Rec_771526,Human_Splice_Rec_771536 RMVar_hsa_circ_5986 76114 RMVar_ID_76114 Human_SNP_ID_274858761 m1A Human chr6 - 43063135 43063135 43063135 TCTCGCCTGTGCACACTCACCGAGGTATGTCCATCCTCATCATACTGCCGCAGCTGCCCCAGGAA TCTCGCCTGTGCACACTCACCGAGGTATGTCCGTCCTCATCATACTGCCGCAGCTGCCCCAGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43062895..43063166 26863196 MeRIP-seq:(Medium) rs771604425 Functional Loss SNV dbSNP153 33..33 33 - - - 76115 RMVar_ID_76115 Human_SNP_ID_274860913 m1A Human chr6 + 43070813 43070813 43070813 ACGCTACTACCAGCGAGCACTGGCCATCTACGAGGGGCAGCTGGGGCCGGACAACCCTAATGTAG ACGCTACTACCAGCGAGCACTGGCCATCTACGGGGGGCAGCTGGGGCCGGACAACCCTAATGTAG A G KLC4 Ensembl:ENSG00000137171 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43070765..43072171 32194978 MeRIP-seq:(Medium) rs1199420805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_771363,Human_Splice_Rec_771389,Human_Splice_Rec_771419,Human_Splice_Rec_771475,Human_Splice_Rec_771507,Human_Splice_Rec_771549,Human_Splice_Rec_771577,Human_Splice_Rec_771585 RMVar_hsa_circ_39894 76116 RMVar_ID_76116 Human_SNP_ID_274861880 m1A Human chr6 + 43073906 43073906 43073906 GCCTCAATTCTTCCGTTTTCCATTGTAGCAGCAACATGAAGCGAGCAGCCTCCTTGAACTATCTG GCCTCAATTCTTCCGTTTTCCATTGTAGCAGCGACATGAAGCGAGCAGCCTCCTTGAACTATCTG A G KLC4 Ensembl:ENSG00000137171 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43073895..43074651 32194978 MeRIP-seq:(Medium) rs1164629902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_771374,Human_Splice_Rec_771375,Human_Splice_Rec_771402,Human_Splice_Rec_771403,Human_Splice_Rec_771432,Human_Splice_Rec_771433,Human_Splice_Rec_771488,Human_Splice_Rec_771489,Human_Splice_Rec_771520,Human_Splice_Rec_771521,Human_Splice_Rec_771562,Human_Splice_Rec_771563,Human_Splice_Rec_771595 RMVar_hsa_circ_39894,RMVar_hsa_circ_87854,RMVar_hsa_circ_238559 76117 RMVar_ID_76117 Human_SNP_ID_274862117 m1A Human chr6 + 43074950 43074950 43074950 GGGTACAAAGCAGGTATGGCCCTCAGAGATGCAGCCTGCTGCTGGCTTTTCAGTCAGAGGGTTGG GGGTACAAAGCAGGTATGGCCCTCAGAGATGCCGCCTGCTGCTGGCTTTTCAGTCAGAGGGTTGG A C KLC4 Ensembl:ENSG00000137171 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43074899..43075049 32194978 MeRIP-seq:(Medium) rs928677557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664967,Human_RBP_ID_5122505,Human_RBP_ID_18171483 Human_miRNA_ID_2099112,Human_miRNA_ID_2105064,Human_miRNA_ID_2111014,Human_miRNA_ID_2163559,Human_miRNA_ID_2220667,Human_miRNA_ID_2483713,Human_miRNA_ID_2594781,Human_miRNA_ID_2737725,Human_miRNA_ID_3038325,Human_miRNA_ID_3072088 RMVar_hsa_circ_87854,RMVar_hsa_circ_238559 76118 RMVar_ID_76118 Human_SNP_ID_274862527 m1A Human chr6 - 43076467 43076467 43076467 GCAGCTCCCATCGCGGCGGGCTCAGGAAAAGGAGCTGAGGGCGCACGGCGGGCGCGCAGACTGCG GCAGCTCCCATCGCGGCGGGCTCAGGAAAAGGTGCTGAGGGCGCACGGCGGGCGCGCAGACTGCG T A lnc-MRPL2-2,lnc-MRPL2-2:2,lnc-MRPL2-2:3 RNACentral:URS0000D5C36B,RNACentral:URS0000D593A4,RNACentral:URS0000D58248 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:43076347..43076479 26863196 MeRIP-seq:(Medium) rs757560914 Functional Loss SNV dbSNP153 33..33 33 - - - 76119 RMVar_ID_76119 Human_SNP_ID_274862575 m1A Human chr6 - 43076535 43076535 43076535 CGCCCAGCAGCGGCAGCAGCAGGACGCTGAGCAGAGGCAACCGGCGGGGTCTGGCCGGGGATCCC CGCCCAGCAGCGGCAGCAGCAGGACGCTGAGCGGAGGCAACCGGCGGGGTCTGGCCGGGGATCCC T C lnc-MRPL2-2,lnc-MRPL2-2:2,lnc-MRPL2-2:3 RNACentral:URS0000D5C36B,RNACentral:URS0000D593A4,RNACentral:URS0000D58248 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43076367..43076575 32194978 MeRIP-seq:(Medium) rs910975535 Functional Loss SNV dbSNP153 33..33 33 - - - 76120 RMVar_ID_76120 Human_SNP_ID_274876891 m1A Human chr6 + 43132529 43132529 43132529 CAAGGGTCTGCCAGAGCCCAGCGTGTGGTGGGAGCACGCGGGAGTCCGGCTGCCCACCCATGGCA CAAGGGTCTGCCAGAGCCCAGCGTGTGGTGGGGGCACGCGGGAGTCCGGCTGCCCACCCATGGCA A G PTK7 Ensembl:ENSG00000112655 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43132001..43132600 32194978 MeRIP-seq:(Medium) rs1198801185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789920,Human_RBP_ID_841562,Human_RBP_ID_951452,Human_RBP_ID_22461286,Human_RBP_ID_22773621 RMVar_hsa_circ_3385,RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_84927,RMVar_hsa_circ_99302,RMVar_hsa_circ_316233,RMVar_hsa_circ_238560,RMVar_hsa_circ_323586,RMVar_hsa_circ_238562,RMVar_hsa_circ_238563,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_90656,RMVar_hsa_circ_110599,RMVar_hsa_circ_238566,RMVar_hsa_circ_238567 76121 RMVar_ID_76121 Human_SNP_ID_274880426 m1A Human chr6 + 43145398 43145398 43145398 GGTGCGGCTCCTGGGGCTGTGCCGGGAGGCTGAGCCCCACTACATGGTGCTGGAATATGTGGATC GGTGCGGCTCCTGGGGCTGTGCCGGGAGGCTGTGCCCCACTACATGGTGCTGGAATATGTGGATC A T PTK7 Ensembl:ENSG00000112655 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43145181..43145400 32194978 MeRIP-seq:(Medium) rs758600953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251321,Human_RBP_ID_18472099,Human_RBP_ID_22773636 Human_Splice_Rec_771685,Human_Splice_Rec_771721,Human_Splice_Rec_771765,Human_Splice_Rec_771799,Human_Splice_Rec_771835,Human_Splice_Rec_771907,Human_Splice_Rec_771945,Human_Splice_Rec_771969,Human_Splice_Rec_772007 Human_miRNA_ID_973302,Human_miRNA_ID_1421248,Human_miRNA_ID_2268930,Human_miRNA_ID_2299915,Human_miRNA_ID_2303183,Human_miRNA_ID_2306447 RMVar_hsa_circ_3385,RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_84927,RMVar_hsa_circ_99302,RMVar_hsa_circ_238560,RMVar_hsa_circ_238563,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_19058,RMVar_hsa_circ_110599,RMVar_hsa_circ_238567,RMVar_hsa_circ_325772,RMVar_hsa_circ_11246,RMVar_hsa_circ_11152,RMVar_hsa_circ_51298,RMVar_hsa_circ_378163 76122 RMVar_ID_76122 Human_SNP_ID_274885046 m1A Human chr6 + 43161499 43161499 43161499 ATGAAGGAGTTTTCAGGAGCTTTTGACACTATATAAACCGCCCTTTTTGTATGCACCACGGGCGG ATGAAGGAGTTTTCAGGAGCTTTTGACACTATGTAAACCGCCCTTTTTGTATGCACCACGGGCGG A G PTK7 Ensembl:ENSG00000112655 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43161476..43161500 32194978 MeRIP-seq:(Medium) rs1398156982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665018,Human_RBP_ID_5122012,Human_RBP_ID_7608493,Human_RBP_ID_15831674,Human_RBP_ID_17664126,Human_RBP_ID_18077004,Human_RBP_ID_18371525,Human_RBP_ID_26715719,Human_RBP_ID_27756243 RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_110599,RMVar_hsa_circ_238567,RMVar_hsa_circ_78053,RMVar_hsa_circ_79476,RMVar_hsa_circ_238571,RMVar_hsa_circ_238572 76123 RMVar_ID_76123 Human_SNP_ID_274885072 m1A Human chr6 + 43161596 43161594 43161597 GGCATGGGAGGTAGGGGTGGGCCCTGGAGATGAGGAGGGTGGGCCATCCTTACCCCACACTTTTA GGCATGGGAGGTAGGGGTGGGCCCTGGAGAT___GAGGGTGGGCCATCCTTACCCCACACTTTTA TGAG T PTK7 Ensembl:ENSG00000112655 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43161546..43161630 26863196 MeRIP-seq:(Medium) rs904039638 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_665021,Human_RBP_ID_841570,Human_RBP_ID_5122013,Human_RBP_ID_5152366,Human_RBP_ID_5532450,Human_RBP_ID_7608502,Human_RBP_ID_9194762,Human_RBP_ID_17663767 RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_110599,RMVar_hsa_circ_238567,RMVar_hsa_circ_78053,RMVar_hsa_circ_79476,RMVar_hsa_circ_238571,RMVar_hsa_circ_238572 76124 RMVar_ID_76124 Human_SNP_ID_274887771 m1A Human chr6 + 43171389 43171376 43171390 GGCCGCGGCCAGCAGCCCCTGCCCCCCGGGGGACGCTGACGGCCGCCCGGCGCGCCGCCCTAGCA GGCCGCGGCCAGCAGCCCCT______________GCTGACGGCCGCCCGGCGCGCCGCCCTAGCA TGCCCCCCGGGGGAC T SRF Ensembl:ENSG00000112658 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43171303..43171469 26863196 MeRIP-seq:(Medium) rs1350733878 Functional Loss DEL dbSNP153 21..34 33 - - - RMVar_hsa_circ_82530,RMVar_hsa_circ_238573 76125 RMVar_ID_76125 Human_SNP_ID_274887784 m1A Human chr6 + 43171389 43171389 43171389 GGCCGCGGCCAGCAGCCCCTGCCCCCCGGGGGACGCTGACGGCCGCCCGGCGCGCCGCCCTAGCA GGCCGCGGCCAGCAGCCCCTGCCCCCCGGGGGCCGCTGACGGCCGCCCGGCGCGCCGCCCTAGCA A C SRF Ensembl:ENSG00000112658 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43171303..43171469 26863196 MeRIP-seq:(Medium) rs1274737964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82530,RMVar_hsa_circ_238573 76126 RMVar_ID_76126 Human_SNP_ID_274887944 m1A Human chr6 + 43171937 43171937 43171937 GGAGTCGGGCGAGGAGGAGGAGCTGGGCGCCGAGCGGCGCGGCCTGAAGCGGAGCCTGAGCGAGA GGAGTCGGGCGAGGAGGAGGAGCTGGGCGCCGGGCGGCGCGGCCTGAAGCGGAGCCTGAGCGAGA A G SRF Ensembl:ENSG00000112658 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:43171276..43172282;chr6:43171276..43175897;chr6:43171276..43175880 26863196 MeRIP-seq:(Medium) rs1416071481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251325,Human_RBP_ID_841580 Human_miRNA_ID_2017700 RMVar_hsa_circ_82530,RMVar_hsa_circ_238573 76127 RMVar_ID_76127 Human_SNP_ID_274888129 m1A Human chr6 + 43172562 43172562 43172562 CTCCGGTGTTCGGACGAGGGCGCCGGAAAAGCAGGGAGCAAACGAGAAGGTATGGAGGTGAGGAG CTCCGGTGTTCGGACGAGGGCGCCGGAAAAGCTGGGAGCAAACGAGAAGGTATGGAGGTGAGGAG A T SRF Ensembl:ENSG00000112658 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43172560..43172654 26863196 MeRIP-seq:(Medium) rs1186266269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82530,RMVar_hsa_circ_238573 76128 RMVar_ID_76128 Human_SNP_ID_274902083 m1A Human chr6 + 43226100 43226100 43226100 CGCTTGTTAAAGGCCACGGCCCGGCCCAGCTCATAGCCTACACCCAAGGATGGCTGTGTCACTTC CGCTTGTTAAAGGCCACGGCCCGGCCCAGCTCGTAGCCTACACCCAAGGATGGCTGTGTCACTTC A G RF00017-4495,RF00017-4633 RNACentral:URS0000923EDC,RNACentral:URS00009644F0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43226076..43226100 26863196 MeRIP-seq:(Medium) rs1562071220 Functional Loss SNV dbSNP153 33..33 33 - - - 76129 RMVar_ID_76129 Human_SNP_ID_274902968 m1A Human chr6 - 43229275 43229275 43229275 GACAGTGCTCACCGAGCACGTGGCGGCCGCCGAGCTGGGCGCGCGCGGTGAGGCCCTGGGGCCGC GACAGTGCTCACCGAGCACGTGGCGGCCGCCGCGCTGGGCGCGCGCGGTGAGGCCCTGGGGCCGC T G DNPH1 Ensembl:ENSG00000112667 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43229251..43229425 32194978 MeRIP-seq:(Medium) rs1320133074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665087,Human_RBP_ID_4904898,Human_RBP_ID_5122276,Human_RBP_ID_8944019,Human_RBP_ID_22461304 Human_Splice_Rec_772361,Human_Splice_Rec_772373 Human_miRNA_ID_2017701 RMVar_hsa_circ_238595,RMVar_hsa_circ_98608 76130 RMVar_ID_76130 Human_SNP_ID_274902985 m1A Human chr6 + 43229311 43229311 43229311 CGGCCGCCACGTGCTCGGTGAGCACTGTCCCGAATCGCCGCAGCCGAGACACGATCCGCTCGTAC CGGCCGCCACGTGCTCGGTGAGCACTGTCCCGCATCGCCGCAGCCGAGACACGATCCGCTCGTAC A C RF00017-4495,RF00017-4633 RNACentral:URS0000923EDC,RNACentral:URS00009644F0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43229052..43229475 26863196 MeRIP-seq:(Medium) rs756528851 Functional Loss SNV dbSNP153 33..33 33 - - - 76131 RMVar_ID_76131 Human_SNP_ID_274903004 m1A Human chr6 - 43229356 43229356 43229356 GTACTTCTGCGGGAGCATTCGCGGCGGACGCGAGGACAGGACGCTGTACGAGCGGATCGTGTCTC GTACTTCTGCGGGAGCATTCGCGGCGGACGCGGGGACAGGACGCTGTACGAGCGGATCGTGTCTC T C DNPH1 Ensembl:ENSG00000112667 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:43229113..43229450 26863196 MeRIP-seq:(Medium) rs1474003608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665089,Human_RBP_ID_842097,Human_RBP_ID_4904050,Human_RBP_ID_5327164,Human_RBP_ID_5478227,Human_RBP_ID_8944019,Human_RBP_ID_22460731,Human_RBP_ID_22514377 Human_Splice_Rec_772361,Human_Splice_Rec_772373 RMVar_hsa_circ_238595,RMVar_hsa_circ_98608 76132 RMVar_ID_76132 Human_SNP_ID_274903050 m1A Human chr6 - 43229425 43229425 43229425 AATGGCTGCTGCCATGGTGCCGGGGCGCAGCGAGAGCTGGGAGCGCGGGGAGCCTGGCCGCCCGG AATGGCTGCTGCCATGGTGCCGGGGCGCAGCGGGAGCTGGGAGCGCGGGGAGCCTGGCCGCCCGG T C DNPH1 Ensembl:ENSG00000112667 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:43229022..43229516;chr6:43229108..43229500 26863196 MeRIP-seq:(Medium) rs1300331488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251338,Human_RBP_ID_789952,Human_RBP_ID_4891165,Human_RBP_ID_5122277,Human_RBP_ID_5151927,Human_RBP_ID_5327164,Human_RBP_ID_8944071,Human_RBP_ID_9336173,Human_RBP_ID_22461305,Human_RBP_ID_27098501 RMVar_hsa_circ_238595,RMVar_hsa_circ_98608 76133 RMVar_ID_76133 Human_SNP_ID_274931669 m1A Human chr6 - 43340351 43340351 43340351 TGAGAAACCAAAGGAGGAGAAGAAAGAAAAAAAGGCAAAGGCTGTGAAAGAAGTAAAGGAGGATG TGAGAAACCAAAGGAGGAGAAGAAAGAAAAAACGGCAAAGGCTGTGAAAGAAGTAAAGGAGGATG T G ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43340300..43340421 26863196 MeRIP-seq:(Medium) rs752857580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40769,RMVar_hsa_circ_66844,RMVar_hsa_circ_107122,RMVar_hsa_circ_51086,RMVar_hsa_circ_54792,RMVar_hsa_circ_112935,RMVar_hsa_circ_123851,RMVar_hsa_circ_238609,RMVar_hsa_circ_238610,RMVar_hsa_circ_238611 76134 RMVar_ID_76134 Human_SNP_ID_274939476 m1A Human chr6 + 43369155 43369155 43369155 GGACGGGGAGACGCGACGACCCCGTGGCGGGGACGGCGAGGCCCGGCGGCCGCGGTGCCCTGAGG GGACGGGGAGACGCGACGACCCCGTGGCGGGGGCGGCGAGGCCCGGCGGCCGCGGTGCCCTGAGG A G RF00017-4495,RF00017-4633 RNACentral:URS0000923EDC,RNACentral:URS00009644F0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:43369043..43369450 26863196 MeRIP-seq:(Medium) rs920540474 Functional Loss SNV dbSNP153 33..33 33 - - - 76135 RMVar_ID_76135 Human_SNP_ID_274953803 m1A Human chr6 + 43427581 43427581 43427581 GGCGTGGCGAATAGCGCCGGCTAGGTCTTCCAACCTCTAGGTGGGGTGCCAGCCGGGGCGGGCCC GGCGTGGCGAATAGCGCCGGCTAGGTCTTCCAGCCTCTAGGTGGGGTGCCAGCCGGGGCGGGCCC A G ABCC10 Ensembl:ENSG00000124574 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43427568..43427807 26863196 MeRIP-seq:(Medium) rs1444010275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903351,Human_RBP_ID_18425438 76136 RMVar_ID_76136 Human_SNP_ID_274953870 m1A Human chr6 - 43427807 43427807 43427807 CAGACCCCGCCCATTCTCGCGGTACCAAGGGTAAAAACGGGAGGAGGTTTCCCCAGTGGATTTCT CAGACCCCGCCCATTCTCGCGGTACCAAGGGTGAAAACGGGAGGAGGTTTCCCCAGTGGATTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43427802..43427945 26863196 MeRIP-seq:(Medium) rs1477576976 Functional Loss SNV dbSNP153 33..33 33 - - - 76137 RMVar_ID_76137 Human_SNP_ID_274955139 m1A Human chr6 + 43432421 43432421 43432421 GCCCTGGTAGCCTTGCTGCCAGCTCCAGCCCTAGTGCTGACCGTGTTGTGGCATTGCCAGCGAGG GCCCTGGTAGCCTTGCTGCCAGCTCCAGCCCTGGTGCTGACCGTGTTGTGGCATTGCCAGCGAGG A G ABCC10 Ensembl:ENSG00000124574 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43432211..43432611 32194978 MeRIP-seq:(Medium) rs1252639201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22461307 RMVar_hsa_circ_14775,RMVar_hsa_circ_266558,RMVar_hsa_circ_320713,RMVar_hsa_circ_238613 76138 RMVar_ID_76138 Human_SNP_ID_274955484 m1A Human chr6 + 43433208 43433208 43433208 ATGAAGCCTGGGGCCTGCCCCTGCAACTGGCCATCACCCTCTACCTGCTGTACCAGCAGGTAGGC ATGAAGCCTGGGGCCTGCCCCTGCAACTGGCCGTCACCCTCTACCTGCTGTACCAGCAGGTAGGC A G ABCC10 Ensembl:ENSG00000124574 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43433158..43433259 32194978 MeRIP-seq:(Medium) rs767825018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9402125,Human_RBP_ID_19018651,Human_RBP_ID_22105155,Human_RBP_ID_27524972 RMVar_hsa_circ_14775,RMVar_hsa_circ_266558,RMVar_hsa_circ_320713,RMVar_hsa_circ_238613 76139 RMVar_ID_76139 Human_SNP_ID_274958175 m1A Human chr6 - 43443052 43443052 43443052 AGAGCAGCCGTGTGGTGTAGCTCAGCATGCCCAGGATGCACCTGTGCAGCAGGTGGTTGGCCACA AGAGCAGCCGTGTGGTGTAGCTCAGCATGCCCTGGATGCACCTGTGCAGCAGGTGGTTGGCCACA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43443003..43443203 32194978 MeRIP-seq:(Medium) rs756016064 Functional Loss SNV dbSNP153 33..33 33 - - - 76140 RMVar_ID_76140 Human_SNP_ID_274961701 m1A Human chr6 + 43454861 43454861 43454861 CAGCGCCGGCCCCAGGAGGGACGGACGGATGGACGGCCGGACGCGTGGACACCTGTGGGACGGCA CAGCGCCGGCCCCAGGAGGGACGGACGGATGGGCGGCCGGACGCGTGGACACCTGTGGGACGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:43454817..43455251 26863196 MeRIP-seq:(Medium) rs1235593834 Functional Loss SNV dbSNP153 33..33 33 - - - 76141 RMVar_ID_76141 Human_SNP_ID_274967756 m1A Human chr6 - 43477630 43477630 43477630 TTCCCCGCCCGACTACTCCAACCCCACAACAAACTTTCCGCCGCTGCCAGCTGCGTTCAGGCCGC TTCCCCGCCCGACTACTCCAACCCCACAACAACCTTTCCGCCGCTGCCAGCTGCGTTCAGGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:43477600..43477872;chr6:43477607..43478259;chr6:43477602..43478085;chr6:43477599..43478045 26863196 MeRIP-seq:(Medium) rs1157804774 Functional Loss SNV dbSNP153 33..33 33 - - - 76142 RMVar_ID_76142 Human_SNP_ID_274972661 m1A Human chr6 - 43499091 43499091 43499091 GCTGTGATACCAGTCTTGCTGACCTCCTGCTCAAGCCGGGATCCAGGAATTTCCAAACGCAGCTC GCTGTGATACCAGTCTTGCTGACCTCCTGCTCGAGCCGGGATCCAGGAATTTCCAAACGCAGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43499041..43499135 26863196 MeRIP-seq:(Medium) rs750751702 Functional Loss SNV dbSNP153 33..33 33 - - - 76143 RMVar_ID_76143 Human_SNP_ID_274973222 m1A Human chr6 + 43501534 43501534 43501534 CTTGATCCCACAACACCCTGCCAGGCTCTTACAGGAGGAGAATGAAGAGCTTCGCCGGCGCCTGG CTTGATCCCACAACACCCTGCCAGGCTCTTACGGGAGGAGAATGAAGAGCTTCGCCGGCGCCTGG A G TJAP1 Ensembl:ENSG00000137221 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43501532..43501603 26863196 MeRIP-seq:(Medium) rs754721586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4891463,Human_RBP_ID_9402132,Human_RBP_ID_19133794,Human_RBP_ID_22482350 Human_Splice_Rec_772818,Human_Splice_Rec_772836,Human_Splice_Rec_772854,Human_Splice_Rec_772872,Human_Splice_Rec_772884,Human_Splice_Rec_772902,Human_Splice_Rec_772920,Human_Splice_Rec_772938,Human_Splice_Rec_772956,Human_Splice_Rec_772974,Human_Splice_Rec_773000,Human_Splice_Rec_773008 RMVar_hsa_circ_42501,RMVar_hsa_circ_238625,RMVar_hsa_circ_346468,RMVar_hsa_circ_351396,RMVar_hsa_circ_274620,RMVar_hsa_circ_238624,RMVar_hsa_circ_346758,RMVar_hsa_circ_50401,RMVar_hsa_circ_308180,RMVar_hsa_circ_49694,RMVar_hsa_circ_288717,RMVar_hsa_circ_58966,RMVar_hsa_circ_296718,RMVar_hsa_circ_238626,RMVar_hsa_circ_238628,RMVar_hsa_circ_374693 76144 RMVar_ID_76144 Human_SNP_ID_274974825 m1A Human chr6 + 43505226 43505226 43505226 AGGTTCGGATCCCCCGCAACAGCCCCCTGCCCAACTGCACTTACGCTACCCGCCAGGCCATTTCC AGGTTCGGATCCCCCGCAACAGCCCCCTGCCCGACTGCACTTACGCTACCCGCCAGGCCATTTCC A G TJAP1 Ensembl:ENSG00000137221 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43505176..43505336 26863196 MeRIP-seq:(Medium) rs1404750650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134354,Human_RBP_ID_17090933 76145 RMVar_ID_76145 Human_SNP_ID_274975705 m1A Human chr6 + 43507655 43507655 43507655 GCCAACACCAGGCTCCGCAAAGCTGTGGGGTAATTTTCTACCATGTCCAGCAGGGTCTGAAGTGG GCCAACACCAGGCTCCGCAAAGCTGTGGGGTAGTTTTCTACCATGTCCAGCAGGGTCTGAAGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43507608..43507855 32194978 MeRIP-seq:(Medium) rs1241862003 Functional Loss SNV dbSNP153 33..33 33 - - - 76146 RMVar_ID_76146 Human_SNP_ID_274977161 m1A Human chr6 + 43511974 43511974 43511974 ACCCATTTTCTGCATTGGCTGCAGAGCCTTGCAGTCCTGGCCAGGAGTTCTTGGCCTTGTGCCTT ACCCATTTTCTGCATTGGCTGCAGAGCCTTGCGGTCCTGGCCAGGAGTTCTTGGCCTTGTGCCTT A G POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43511924..43512024 32194978 MeRIP-seq:(Medium) rs1433880301 Functional Loss SNV dbSNP153 33..33 33 - - - 76147 RMVar_ID_76147 Human_SNP_ID_274977503 m1A Human chr6 + 43512871 43512871 43512871 GAACAGGACAATGCAATGCCCAAAGAGGCCATAGCCCTGGGAAGGAGGATGGTGGAGAGGAAAAT GAACAGGACAATGCAATGCCCAAAGAGGCCATCGCCCTGGGAAGGAGGATGGTGGAGAGGAAAAT A C POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43512738..43512936 32194978 MeRIP-seq:(Medium) rs1489465307 Functional Loss SNV dbSNP153 33..33 33 - - - 76148 RMVar_ID_76148 Human_SNP_ID_274978485 m1A Human chr6 - 43515956 43515956 43515956 CGCTGATGCAGCTGATGCAGCTGCTGCTGAAGAGGAGGATGGAGAGTTCCTGGGCATGAAGGGCT CGCTGATGCAGCTGATGCAGCTGCTGCTGAAGGGGAGGATGGAGAGTTCCTGGGCATGAAGGGCT T C YIPF3 Ensembl:ENSG00000137207 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:43515609..43516140 26863196 MeRIP-seq:(Medium) rs931373374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7608796,Human_RBP_ID_15832605,Human_RBP_ID_19017097,Human_RBP_ID_22461316,Human_RBP_ID_22618509,Human_RBP_ID_24164080 Human_Splice_Rec_773257,Human_Splice_Rec_773273,Human_Splice_Rec_773289,Human_Splice_Rec_773305,Human_Splice_Rec_773325,Human_Splice_Rec_773345,Human_Splice_Rec_773352,Human_Splice_Rec_773353,Human_Splice_Rec_773365,Human_Splice_Rec_773393,Human_Splice_Rec_773399,Human_Splice_Rec_773405 RMVar_hsa_circ_51302,RMVar_hsa_circ_238636 76149 RMVar_ID_76149 Human_SNP_ID_274978540 m1A Human chr6 + 43516070 43516070 43516070 AGCTAGAGCCTGAGGTATCATCCATGTTCTCCATGTCAATCACAGCTGAGCCTCCGCCCTGTGAA AGCTAGAGCCTGAGGTATCATCCATGTTCTCCGTGTCAATCACAGCTGAGCCTCCGCCCTGTGAA A G POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43515626..43516142 26863196 MeRIP-seq:(Medium) rs147018912 Functional Loss SNV dbSNP153 33..33 33 - - - 76150 RMVar_ID_76150 Human_SNP_ID_274978779 m1A Human chr6 - 43516796 43516796 43516796 CGACGGGAGCCCTCAAGGGACATGGCAACTACAGCGGCGCCGGCGGGCGGCGCCCGAAATGGAGC CGACGGGAGCCCTCAAGGGACATGGCAACTACTGCGGCGCCGGCGGGCGGCGCCCGAAATGGAGC T A YIPF3 Ensembl:ENSG00000137207 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43516726..43516800 26863196 MeRIP-seq:(Medium) rs770552961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252242,Human_RBP_ID_1047803,Human_RBP_ID_4904055,Human_RBP_ID_18077154,Human_RBP_ID_18195600,Human_RBP_ID_27098652 Human_Splice_Rec_773255,Human_Splice_Rec_773271,Human_Splice_Rec_773287,Human_Splice_Rec_773303,Human_Splice_Rec_773323,Human_Splice_Rec_773343,Human_Splice_Rec_773351,Human_Splice_Rec_773363,Human_Splice_Rec_773403 76151 RMVar_ID_76151 Human_SNP_ID_274978807 m1A Human chr6 - 43516870 43516870 43516870 CTCGACCCTGGACGTCTACCTTCCGGAGGCCCACATCTTGCCCACTCCGCGCGCGGGGCTAGCGC CTCGACCCTGGACGTCTACCTTCCGGAGGCCCTCATCTTGCCCACTCCGCGCGCGGGGCTAGCGC T A YIPF3 Ensembl:ENSG00000137207 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43516726..43516925 26863196 MeRIP-seq:(Medium) rs908705048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252242,Human_RBP_ID_4903355,Human_RBP_ID_5511750,Human_RBP_ID_18077155,Human_RBP_ID_22460733 76152 RMVar_ID_76152 Human_SNP_ID_274978808 m1A Human chr6 - 43516870 43516870 43516870 CTCGACCCTGGACGTCTACCTTCCGGAGGCCCACATCTTGCCCACTCCGCGCGCGGGGCTAGCGC CTCGACCCTGGACGTCTACCTTCCGGAGGCCCGCATCTTGCCCACTCCGCGCGCGGGGCTAGCGC T C YIPF3 Ensembl:ENSG00000137207 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43516726..43516925 26863196 MeRIP-seq:(Medium) rs908705048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252242,Human_RBP_ID_4903355,Human_RBP_ID_5511750,Human_RBP_ID_18077155,Human_RBP_ID_22460733 76153 RMVar_ID_76153 Human_SNP_ID_274978815 m1A Human chr6 + 43516881 43516881 43516881 GCGCGCGGAGTGGGCAAGATGTGGGCCTCCGGAAGGTAGACGTCCAGGGTCGAGGAGAGGTGGGA GCGCGCGGAGTGGGCAAGATGTGGGCCTCCGGCAGGTAGACGTCCAGGGTCGAGGAGAGGTGGGA A C POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43516851..43516925 26863196 MeRIP-seq:(Medium) rs921494460 Functional Loss SNV dbSNP153 33..33 33 - - - 76154 RMVar_ID_76154 Human_SNP_ID_274980747 m1A Human chr6 + 43522572 43522572 43522572 TGAGATCGCCTTCACGATCCACAGAAACCCAGAGCACCACACAGGAAGAGGGAGCAACACAAGAC TGAGATCGCCTTCACGATCCACAGAAACCCAGGGCACCACACAGGAAGAGGGAGCAACACAAGAC A G POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43522478..43522579 32194978 MeRIP-seq:(Medium) rs1489181171 Functional Loss SNV dbSNP153 33..33 33 - - - 76155 RMVar_ID_76155 Human_SNP_ID_274980823 m1A Human chr6 - 43522727 43522727 43522727 GCTCTGCACAAAAACAGACCTGTTGTCCATCCAGTCCACTGACAAGAGGGTTTCCCCGAGAGCCG GCTCTGCACAAAAACAGACCTGTTGTCCATCCGGTCCACTGACAAGAGGGTTTCCCCGAGAGCCG T C XPO5 Ensembl:ENSG00000124571 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43522678..43523127 32194978 MeRIP-seq:(Medium) rs757817181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15832791 Human_miRNA_ID_131057,Human_miRNA_ID_1980358,Human_miRNA_ID_1982085 RMVar_hsa_circ_238641,RMVar_hsa_circ_77281 76156 RMVar_ID_76156 Human_SNP_ID_274980824 m1A Human chr6 - 43522727 43522727 43522727 GCTCTGCACAAAAACAGACCTGTTGTCCATCCAGTCCACTGACAAGAGGGTTTCCCCGAGAGCCG GCTCTGCACAAAAACAGACCTGTTGTCCATCCCGTCCACTGACAAGAGGGTTTCCCCGAGAGCCG T G XPO5 Ensembl:ENSG00000124571 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43522678..43523127 32194978 MeRIP-seq:(Medium) rs757817181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15832791 Human_miRNA_ID_131057,Human_miRNA_ID_1980358,Human_miRNA_ID_1982085 RMVar_hsa_circ_238641,RMVar_hsa_circ_77281 76157 RMVar_ID_76157 Human_SNP_ID_274981559 m1A Human chr6 - 43525139 43525139 43525139 CCTGGAAAGATACTCTGTCCTGCCAGAGGACAACCTCACAGCTCTGCTGGCCTCTCCTCAAACAA CCTGGAAAGATACTCTGTCCTGCCAGAGGACAGCCTCACAGCTCTGCTGGCCTCTCCTCAAACAA T C XPO5 Ensembl:ENSG00000124571 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43525132..43525232 32194978 MeRIP-seq:(Medium) rs1164580675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9194795,Human_RBP_ID_9309724 Human_Splice_Rec_773460,Human_Splice_Rec_773461,Human_Splice_Rec_773474,Human_Splice_Rec_773475,Human_Splice_Rec_773486,Human_Splice_Rec_773487,Human_Splice_Rec_773500,Human_Splice_Rec_773501 Human_miRNA_ID_2006638,Human_miRNA_ID_2254458,Human_miRNA_ID_2672256 RMVar_hsa_circ_103100,RMVar_hsa_circ_238641,RMVar_hsa_circ_77281,RMVar_hsa_circ_283179,RMVar_hsa_circ_293341,RMVar_hsa_circ_267792,RMVar_hsa_circ_103908,RMVar_hsa_circ_238642,RMVar_hsa_circ_238643 76158 RMVar_ID_76158 Human_SNP_ID_274981755 m1A Human chr6 - 43525895 43525895 43525895 TAACAGATGAAGAAATGATGGCCACAGAGGTCACCCCCTCAGCTATGGCAGAGCTTACAGACCTG TAACAGATGAAGAAATGATGGCCACAGAGGTCTCCCCCTCAGCTATGGCAGAGCTTACAGACCTG T A XPO5 Ensembl:ENSG00000124571 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43525780..43525980 32194978 MeRIP-seq:(Medium) rs778055808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842004,Human_RBP_ID_5398879,Human_RBP_ID_9309725,Human_RBP_ID_9350530,Human_RBP_ID_9400583,Human_RBP_ID_19017101,Human_RBP_ID_22462769,Human_RBP_ID_22682919 Human_Splice_Rec_773458,Human_Splice_Rec_773459,Human_Splice_Rec_773472,Human_Splice_Rec_773473,Human_Splice_Rec_773484,Human_Splice_Rec_773485,Human_Splice_Rec_773498,Human_Splice_Rec_773499 Human_miRNA_ID_1561846 RMVar_hsa_circ_27844,RMVar_hsa_circ_103100,RMVar_hsa_circ_238641,RMVar_hsa_circ_77281,RMVar_hsa_circ_283179,RMVar_hsa_circ_267792,RMVar_hsa_circ_91137,RMVar_hsa_circ_103908,RMVar_hsa_circ_238642,RMVar_hsa_circ_238643,RMVar_hsa_circ_354404,RMVar_hsa_circ_33944,RMVar_hsa_circ_238644 76159 RMVar_ID_76159 Human_SNP_ID_275007749 m1A Human chr6 - 43621093 43621093 43621093 GGTGGTGGCGGCCCAGAGTCTGAAGAAATGGCACAGGGACAGTGAATGGTAGTGTTGCCACCCTG GGTGGTGGCGGCCCAGAGTCTGAAGAAATGGCCCAGGGACAGTGAATGGTAGTGTTGCCACCCTG T G GTPBP2 Ensembl:ENSG00000172432 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43621044..43621194 32194978 MeRIP-seq:(Medium) rs1212333983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665273,Human_RBP_ID_15834474,Human_RBP_ID_27525054 Human_miRNA_ID_977254 76160 RMVar_ID_76160 Human_SNP_ID_275009191 m1A Human chr6 + 43626265 43626265 43626265 CCATCCGGTGCAGGGTCTTGAGCGAAGCTCGCATTTCCTCCTCAGCCAGCCCCACCAGCAGCCCA CCATCCGGTGCAGGGTCTTGAGCGAAGCTCGCGTTTCCTCCTCAGCCAGCCCCACCAGCAGCCCA A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43625751..43626963 26863196 MeRIP-seq:(Medium) rs1244133220 Functional Loss SNV dbSNP153 33..33 33 - - - 76161 RMVar_ID_76161 Human_SNP_ID_275009724 m1A Human chr6 + 43628672 43628672 43628672 AGGATGCAGTCTCTCTTGCCCTATGGCGGCACACGCAGTTGGTCGGGGTGCTCTTCCTGGGATCC AGGATGCAGTCTCTCTTGCCCTATGGCGGCACGCGCAGTTGGTCGGGGTGCTCTTCCTGGGATCC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43628670..43628816 26863196 MeRIP-seq:(Medium) rs967394108 Functional Loss SNV dbSNP153 33..33 33 - - - 76162 RMVar_ID_76162 Human_SNP_ID_275009889 m1A Human chr6 - 43629035 43629035 43629035 CAGCAGCGGCTGCGGGGGGCCAAAGGGAAAGAAGAAGAACGGAAGGAACAGAGGGGGCAAAGCCA CAGCAGCGGCTGCGGGGGGCCAAAGGGAAAGAGGAAGAACGGAAGGAACAGAGGGGGCAAAGCCA T C GTPBP2 Ensembl:ENSG00000172432 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:43628909..43629255;chr6:43628857..43629241 26863196 MeRIP-seq:(Medium) rs1470049137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_215467,Human_RBP_ID_267325,Human_RBP_ID_949692,Human_RBP_ID_1678571,Human_RBP_ID_3969150,Human_RBP_ID_4891919,Human_RBP_ID_5327470,Human_RBP_ID_5398893,Human_RBP_ID_9437472,Human_RBP_ID_18425659,Human_RBP_ID_19018721,Human_RBP_ID_21991757,Human_RBP_ID_23067367,Human_RBP_ID_24164272,Human_RBP_ID_24554636,Human_RBP_ID_26355216,Human_RBP_ID_27098778,Human_RBP_ID_27827694 Human_Splice_Rec_773655,Human_Splice_Rec_773695 76163 RMVar_ID_76163 Human_SNP_ID_275009900 m1A Human chr6 + 43629057 43629057 43629057 TCCGTTCTTCTTCTTTCCCTTTGGCCCCCCGCAGCCGCTGCTGCTGCCGGCCCCCCTAGCCTTGA TCCGTTCTTCTTCTTTCCCTTTGGCCCCCCGCCGCCGCTGCTGCTGCCGGCCCCCCTAGCCTTGA A C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:43628932..43629275;chr6:43629001..43629225 26863196 MeRIP-seq:(Medium) rs966869997 Functional Loss SNV dbSNP153 33..33 33 - - - 76164 RMVar_ID_76164 Human_SNP_ID_275009938 m1A Human chr6 + 43629129 43629129 43629129 GCCCACGGCCGGGCCCCCTCCGGGCCGGCAGCAGCCGCCGAACAGCTCCGATACCCGCGAGTCCA GCCCACGGCCGGGCCCCCTCCGGGCCGGCAGCGGCCGCCGAACAGCTCCGATACCCGCGAGTCCA A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:43629040..43629225 26863196 MeRIP-seq:(Medium) rs759820443 Functional Loss SNV dbSNP153 33..33 33 - - - 76165 RMVar_ID_76165 Human_SNP_ID_275009952 m1A Human chr6 - 43629148 43629148 43629148 GGCTGGCGGCAGCGGCGGATGGACTCGCGGGTATCGGAGCTGTTCGGCGGCTGCTGCCGGCCCGG GGCTGGCGGCAGCGGCGGATGGACTCGCGGGTGTCGGAGCTGTTCGGCGGCTGCTGCCGGCCCGG T C GTPBP2 Ensembl:ENSG00000172432 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43628976..43629208 26863196 MeRIP-seq:(Medium) rs1456228989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463,Human_RBP_ID_81884,Human_RBP_ID_791126,Human_RBP_ID_4914299,Human_RBP_ID_5090309,Human_RBP_ID_5399761,Human_RBP_ID_9336179,Human_RBP_ID_9438464,Human_RBP_ID_19018722,Human_RBP_ID_22514404,Human_RBP_ID_23067368,Human_RBP_ID_27098780 76166 RMVar_ID_76166 Human_SNP_ID_275009953 m1A Human chr6 + 43629149 43629149 43629149 CGGGCCGGCAGCAGCCGCCGAACAGCTCCGATACCCGCGAGTCCATCCGCCGCTGCCGCCAGCCC CGGGCCGGCAGCAGCCGCCGAACAGCTCCGATCCCCGCGAGTCCATCCGCCGCTGCCGCCAGCCC A C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:43629047..43629208 26863410 MeRIP-seq:(Medium) rs919995673 Functional Loss SNV dbSNP153 33..33 33 - - - 76167 RMVar_ID_76167 Human_SNP_ID_275020955 m1A Human chr6 + 43671449 43671449 43671449 CCTGCACTTCCCAAGCAGTGAGCGCACACCCAATGGGTAAGCCCATGAACCCAGTTTATGACACT CCTGCACTTCCCAAGCAGTGAGCGCACACCCACTGGGTAAGCCCATGAACCCAGTTTATGACACT A C RSPH9 Ensembl:ENSG00000172426 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43671401..43671500 32194978 MeRIP-seq:(Medium) rs970756981 Functional Loss SNV dbSNP153 33..33 33 - - - 76168 RMVar_ID_76168 Human_SNP_ID_275020956 m1A Human chr6 + 43671449 43671449 43671449 CCTGCACTTCCCAAGCAGTGAGCGCACACCCAATGGGTAAGCCCATGAACCCAGTTTATGACACT CCTGCACTTCCCAAGCAGTGAGCGCACACCCATTGGGTAAGCCCATGAACCCAGTTTATGACACT A T RSPH9 Ensembl:ENSG00000172426 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43671401..43671500 32194978 MeRIP-seq:(Medium) rs970756981 Functional Loss SNV dbSNP153 33..33 33 - - - 76169 RMVar_ID_76169 Human_SNP_ID_275021021 m1A Human chr6 + 43671736 43671734 43671736 GTGGGCCTCCTACTCCCCAGCACAGGTGCAGGAGGAACTCTGGAAGCACTGCTCTCTGTCAGTGA GTGGGCCTCCTACTCCCCAGCACAGGTGCAG__GGAACTCTGGAAGCACTGCTCTCTGTCAGTGA GGA G RSPH9 Ensembl:ENSG00000172426 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43671308..43675289 32194978 MeRIP-seq:(Medium) rs1293653228 Functional Loss DEL dbSNP153 32..33 33 - - - 76170 RMVar_ID_76170 Human_SNP_ID_275021022 m1A Human chr6 + 43671736 43671736 43671736 GTGGGCCTCCTACTCCCCAGCACAGGTGCAGGAGGAACTCTGGAAGCACTGCTCTCTGTCAGTGA GTGGGCCTCCTACTCCCCAGCACAGGTGCAGGGGGAACTCTGGAAGCACTGCTCTCTGTCAGTGA A G RSPH9 Ensembl:ENSG00000172426 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43671308..43675289 32194978 MeRIP-seq:(Medium) rs1183313653 Functional Loss SNV dbSNP153 33..33 33 - - - 76171 RMVar_ID_76171 Human_SNP_ID_275022809 m1A Human chr6 - 43678625 43678625 43678625 TCTCACACTGGCTCACTTTCTCTGTCTCCTAGATTGAAGGCCGTATCACAGCGACTCCCAAGGAG TCTCACACTGGCTCACTTTCTCTGTCTCCTAGGTTGAAGGCCGTATCACAGCGACTCCCAAGGAG T C MRPS18A Ensembl:ENSG00000096080 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43678576..43678650 26863196 MeRIP-seq:(Medium) rs767507852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948789,Human_RBP_ID_19131288 Human_Splice_Rec_773736,Human_Splice_Rec_773746,Human_Splice_Rec_773754 RMVar_hsa_circ_42286,RMVar_hsa_circ_81708,RMVar_hsa_circ_238724,RMVar_hsa_circ_125028,RMVar_hsa_circ_238727 76172 RMVar_ID_76172 Human_SNP_ID_275024874 m1A Human chr6 + 43687696 43687696 43687696 TCACCTTCCCTGAACCCGCGAGCTGGAAGCCGAGACCAGCTGGTCGCTGCCGGGCCCGCTAGTAG TCACCTTCCCTGAACCCGCGAGCTGGAAGCCGGGACCAGCTGGTCGCTGCCGGGCCCGCTAGTAG A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43681095..43687742 32194978 MeRIP-seq:(Medium) rs1326207079 Functional Loss SNV dbSNP153 33..33 33 - - - 76173 RMVar_ID_76173 Human_SNP_ID_275024905 m1A Human chr6 + 43687747 43687747 43687747 GGGCCCGCTAGTAGCCCACGGAGAAGCCGCCCACAGCCGGACACCAGAGCCTTGAGGGCCGCCAT GGGCCCGCTAGTAGCCCACGGAGAAGCCGCCCGCAGCCGGACACCAGAGCCTTGAGGGCCGCCAT A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:43687615..43687800 26863196 MeRIP-seq:(Medium) rs761485104 Functional Loss SNV dbSNP153 33..33 33 - - - 76174 RMVar_ID_76174 Human_SNP_ID_275045272 m1A Human chr6 - 43771122 43771122 43771122 CTACTCTTCCTCCCCGGCCCGAGGCCCGGGCCAGGGCCTGGGGAGCGCGCGCGGCTGGAGCACTG CTACTCTTCCTCCCCGGCCCGAGGCCCGGGCCGGGGCCTGGGGAGCGCGCGCGGCTGGAGCACTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43771101..43771125 26863196 MeRIP-seq:(Medium) rs1348253363 Functional Loss SNV dbSNP153 33..33 33 - - - 76175 RMVar_ID_76175 Human_SNP_ID_275046949 m1A Human chr6 + 43777725 43777725 43777725 GGGGGGATAGGGAGGGGGGTAACACTTTGGGAACAGGTGGTCCCAGGTCGTTTCCTGGCTAGATT GGGGGGATAGGGAGGGGGGTAACACTTTGGGAGCAGGTGGTCCCAGGTCGTTTCCTGGCTAGATT A G VEGFA Ensembl:ENSG00000112715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43777720..43777814 26863196 MeRIP-seq:(Medium) rs1219979424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79816,Human_RBP_ID_789998,Human_RBP_ID_841263,Human_RBP_ID_947738,Human_RBP_ID_3822187,Human_RBP_ID_3969154,Human_RBP_ID_5090314,Human_RBP_ID_5122281,Human_RBP_ID_5217309,Human_RBP_ID_5398262,Human_RBP_ID_8143751,Human_RBP_ID_8237122,Human_RBP_ID_9350236,Human_RBP_ID_9437477,Human_RBP_ID_9444317,Human_RBP_ID_17663140,Human_RBP_ID_18957483,Human_RBP_ID_19129447,Human_RBP_ID_22105187,Human_RBP_ID_22365559,Human_RBP_ID_22418770,Human_RBP_ID_22682940,Human_RBP_ID_22746261,Human_RBP_ID_22773096,Human_RBP_ID_24436359,Human_RBP_ID_26354020,Human_RBP_ID_26771991,Human_RBP_ID_26792448 RMVar_hsa_circ_33572,RMVar_hsa_circ_238728,RMVar_hsa_circ_102569,RMVar_hsa_circ_322948,RMVar_hsa_circ_74333,RMVar_hsa_circ_350327,RMVar_hsa_circ_324506,RMVar_hsa_circ_238730 76176 RMVar_ID_76176 Human_SNP_ID_275047533 m1A Human chr6 + 43779985 43779976 43779985 GCTCGGAAGAGTGTCTGGTGAGATGGTGTAGCAGGCTTTGACAGGCTGGGGAGAGAACTCCCTGC GCTCGGAAGAGTGTCTGGTGAGAT_________GGCTTTGACAGGCTGGGGAGAGAACTCCCTGC TGGTGTAGCA T VEGFA Ensembl:ENSG00000112715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43779982..43780113 26863196 MeRIP-seq:(Medium) rs140885721 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_74333,RMVar_hsa_circ_350327 76177 RMVar_ID_76177 Human_SNP_ID_275047672 m1A Human chr6 + 43780524 43780524 43780524 GCCATCCCATGGTGGGCAGCGTGAGGAGAAGAAAGAGCCATCGAGTGCTTGCTGCCCAGACACGC GCCATCCCATGGTGGGCAGCGTGAGGAGAAGAGAGAGCCATCGAGTGCTTGCTGCCCAGACACGC A G VEGFA Ensembl:ENSG00000112715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43780522..43780613 26863196 MeRIP-seq:(Medium) rs1225245792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090323 RMVar_hsa_circ_74333,RMVar_hsa_circ_350327 76178 RMVar_ID_76178 Human_SNP_ID_275048841 m1A Human chr6 + 43784632 43784632 43784632 GAACCAGATCTCTCACCAGGAAAGACTGATACAGAACGATCGATACAGAAACCACGCTGCCGCCA GAACCAGATCTCTCACCAGGAAAGACTGATACGGAACGATCGATACAGAAACCACGCTGCCGCCA A G VEGFA Ensembl:ENSG00000112715 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:43784581..43784739 26863196 MeRIP-seq:(Medium) rs1249577551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1673971,Human_RBP_ID_17309909,Human_RBP_ID_18084909,Human_RBP_ID_23067387,Human_RBP_ID_26355229 Human_Splice_Rec_773780,Human_Splice_Rec_773792,Human_Splice_Rec_773800,Human_Splice_Rec_773824,Human_Splice_Rec_773838,Human_Splice_Rec_773850,Human_Splice_Rec_773864,Human_Splice_Rec_773874,Human_Splice_Rec_773884,Human_Splice_Rec_773896,Human_Splice_Rec_773910,Human_Splice_Rec_773932,Human_Splice_Rec_773944,Human_Splice_Rec_773956,Human_Splice_Rec_773970,Human_Splice_Rec_773992,Human_Splice_Rec_774004,Human_Splice_Rec_774014,Human_Splice_Rec_774018,Human_Splice_Rec_774024 76179 RMVar_ID_76179 Human_SNP_ID_275048860 m1A Human chr6 - 43784657 43784657 43784657 TGTTCTGTCGATGGTGATGGTGTGGTGGCGGCAGCGTGGTTTCTGTATCGATCGTTCTGTATCAG TGTTCTGTCGATGGTGATGGTGTGGTGGCGGCGGCGTGGTTTCTGTATCGATCGTTCTGTATCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43784522..43784823 26863196 MeRIP-seq:(Medium) rs111933757 Functional Loss SNV dbSNP153 33..33 33 - - - 76180 RMVar_ID_76180 Human_SNP_ID_275049112 m1A Human chr6 + 43785646 43785646 43785646 CACACCATTGAAACCACTAGTTCTGTCCCCCCAGGAGACCTGGTTGTGTGTGTGTGAGTGGTTGA CACACCATTGAAACCACTAGTTCTGTCCCCCCCGGAGACCTGGTTGTGTGTGTGTGAGTGGTTGA A C VEGFA Ensembl:ENSG00000112715 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:43785597..43785775 26863196 MeRIP-seq:(Medium) rs1054700031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24164329 Human_miRNA_ID_255615 76181 RMVar_ID_76181 Human_SNP_ID_275049121 m1A Human chr6 + 43785678 43785678 43785678 AGGAGACCTGGTTGTGTGTGTGTGAGTGGTTGACCTTCCTCCATCCCCTGGTCCTTCCCTTCCCT AGGAGACCTGGTTGTGTGTGTGTGAGTGGTTGGCCTTCCTCCATCCCCTGGTCCTTCCCTTCCCT A G VEGFA Ensembl:ENSG00000112715 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1328747281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252098,Human_RBP_ID_665320,Human_RBP_ID_792056,Human_RBP_ID_5532498,Human_RBP_ID_18077346,Human_RBP_ID_24164330,Human_RBP_ID_27525136 Human_miRNA_ID_1424683,Human_miRNA_ID_1492627 76182 RMVar_ID_76182 Human_SNP_ID_275102471 m1A Human chr6 + 44000674 44000674 44000674 GCGCCCTGGCCCAAGGAGGAGGCCCTTCAGCAACGGAGTGGGCCTGCATTCTGCGGAGGGTGAGA GCGCCCTGGCCCAAGGAGGAGGCCCTTCAGCAGCGGAGTGGGCCTGCATTCTGCGGAGGGTGAGA A G C6orf223 Ensembl:ENSG00000181577 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44000625..44000737 26863196 MeRIP-seq:(Medium) rs1289039225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_774069,Human_Splice_Rec_774075,Human_Splice_Rec_774081 76183 RMVar_ID_76183 Human_SNP_ID_275103327 m1A Human chr6 - 44003002 44003002 44003002 TGTAATTTCTTCTCGCGCTCGGGGTGTGTTGTAGGAGGCGAAGCGATGCCGGCTTGGCTGAGTCA TGTAATTTCTTCTCGCGCTCGGGGTGTGTTGTGGGAGGCGAAGCGATGCCGGCTTGGCTGAGTCA T C AL109615.3 Ensembl:ENSG00000237686 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44002955..44003133 26863196 MeRIP-seq:(Medium) rs897661938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106005,RMVar_hsa_circ_238732 76184 RMVar_ID_76184 Human_SNP_ID_275105192 m1A Human chr6 + 44009751 44009751 44009751 GAAGGGAAAGGGAAGGGGGGAAGAAAGGAAGAAAGAGAGTTGAGCATGCCTTGAATGCTCTGAAG GAAGGGAAAGGGAAGGGGGGAAGAAAGGAAGAGAGAGAGTTGAGCATGCCTTGAATGCTCTGAAG A G lnc-C6orf223-1 RNACentral:URS00009C3AE1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44009739..44009830 26863196 MeRIP-seq:(Medium) rs945596783 Functional Loss SNV dbSNP153 33..33 33 - - - 76185 RMVar_ID_76185 Human_SNP_ID_275106094 m1A Human chr6 + 44013932 44013932 44013932 CAGGCTTTGGAAAGGAGAGCAGTGGAAGATGGAGGATGAAAGGAAGGTGACCTGAGGCTAGATCA CAGGCTTTGGAAAGGAGAGCAGTGGAAGATGGCGGATGAAAGGAAGGTGACCTGAGGCTAGATCA A C lnc-C6orf223-1,lnc-C6orf223-4 RNACentral:URS00009C3AE1,RNACentral:URS00008B9FAF lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44013699..44013941 26863196 MeRIP-seq:(Medium) rs1312917549 Functional Loss SNV dbSNP153 33..33 33 - - - 76186 RMVar_ID_76186 Human_SNP_ID_275122910 m1A Human chr6 + 44085012 44085012 44085012 AAGAAACAGCTGCAGAGCAGCCAGAGGACAGCAACCCTACCCCAGAAATGGACATGAGAGATAAA AAGAAACAGCTGCAGAGCAGCCAGAGGACAGCCACCCTACCCCAGAAATGGACATGAGAGATAAA A C AL109615.2 Ensembl:ENSG00000231881 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44085005..44085076 26863196 MeRIP-seq:(Medium) rs1040352579 Functional Loss SNV dbSNP153 33..33 33 - - - 76187 RMVar_ID_76187 Human_SNP_ID_275126054 m1A Human chr6 - 44097734 44097734 44097734 TGGGCAGAGGAAGAGAAATGGGAAAATGCAGGAAACTGGGATAGTTCTGTGGGAGGAGAAGGGAG TGGGCAGAGGAAGAGAAATGGGAAAATGCAGGGAACTGGGATAGTTCTGTGGGAGGAGAAGGGAG T C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44097685..44097838 26863196 MeRIP-seq:(Medium) rs1011125425 Functional Loss SNV dbSNP153 33..33 33 - - - 76188 RMVar_ID_76188 Human_SNP_ID_275126055 m1A Human chr6 - 44097734 44097734 44097734 TGGGCAGAGGAAGAGAAATGGGAAAATGCAGGAAACTGGGATAGTTCTGTGGGAGGAGAAGGGAG TGGGCAGAGGAAGAGAAATGGGAAAATGCAGGCAACTGGGATAGTTCTGTGGGAGGAGAAGGGAG T G RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44097685..44097838 26863196 MeRIP-seq:(Medium) rs1011125425 Functional Loss SNV dbSNP153 33..33 33 - - - 76189 RMVar_ID_76189 Human_SNP_ID_275126833 m1A Human chr6 - 44100980 44100980 44100980 AGAGGGAAGGTGAGGATGGAGAAAGGGTTATCAGTGTACTGAGGGCGCTACGCCCCGTGATCTCC AGAGGGAAGGTGAGGATGGAGAAAGGGTTATCGGTGTACTGAGGGCGCTACGCCCCGTGATCTCC T C RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44100903..44101005 26863196 MeRIP-seq:(Medium) rs1562093154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3008700,Human_RBP_ID_15835297,Human_RBP_ID_24164384 76190 RMVar_ID_76190 Human_SNP_ID_275127119 m1A Human chr6 + 44102162 44102162 44102162 TCCCATCTCCTTGACTGTCTTCTTGACTCCCCACCCAGCTTCTTCCTGCCCACCTGCCTCCTAAA TCCCATCTCCTTGACTGTCTTCTTGACTCCCCGCCCAGCTTCTTCCTGCCCACCTGCCTCCTAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:44101882..44102443 26863196 MeRIP-seq:(Medium) rs991648253 Functional Loss SNV dbSNP153 33..33 33 - - - 76191 RMVar_ID_76191 Human_SNP_ID_275129961 m1A Human chr6 - 44113918 44113918 44113918 AACGGGAACCCTGTGGGGACACGAATTAAGACACCCATCCCCACCAGCCTGCGCAAGCGGGAAGG AACGGGAACCCTGTGGGGACACGAATTAAGACGCCCATCCCCACCAGCCTGCGCAAGCGGGAAGG T C MRPL14 Ensembl:ENSG00000180992 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44113801..44114059 26863196 MeRIP-seq:(Medium) rs763539119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4892175,Human_RBP_ID_18077425,Human_RBP_ID_19018749,Human_RBP_ID_22462110,Human_RBP_ID_22514410,Human_RBP_ID_24164419 Human_miRNA_ID_2051053,Human_miRNA_ID_2725234 RMVar_hsa_circ_77917,RMVar_hsa_circ_238733 76192 RMVar_ID_76192 Human_SNP_ID_275129963 m1A Human chr6 + 44113924 44113924 44113924 CGCTTGCGCAGGCTGGTGGGGATGGGTGTCTTAATTCGTGTCCCCACAGGGTTCCCGTTGTCCTC CGCTTGCGCAGGCTGGTGGGGATGGGTGTCTTCATTCGTGTCCCCACAGGGTTCCCGTTGTCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44113835..44114128 26863196 MeRIP-seq:(Medium) rs887707018 Functional Loss SNV dbSNP153 33..33 33 - - - 76193 RMVar_ID_76193 Human_SNP_ID_275130078 m1A Human chr6 - 44114183 44114183 44114183 CACCAGCACCACTGGGAGTCTGAGTGCGATTCAGAAGATGACGCGGGTACGAGTGGTGGACAACA CACCAGCACCACTGGGAGTCTGAGTGCGATTCGGAAGATGACGCGGGTACGAGTGGTGGACAACA T C MRPL14 Ensembl:ENSG00000180992 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:44114133..44127425;chr6:44113776..44114229;chr6:44113820..44114246 26863196 MeRIP-seq:(Medium) rs1481887902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665356,Human_RBP_ID_1674025,Human_RBP_ID_2021998,Human_RBP_ID_4892192,Human_RBP_ID_5122026,Human_RBP_ID_18866594,Human_RBP_ID_22831906,Human_RBP_ID_23259167,Human_RBP_ID_24164422,Human_RBP_ID_26039257 Human_Splice_Rec_774096 RMVar_hsa_circ_77917,RMVar_hsa_circ_238733 76194 RMVar_ID_76194 Human_SNP_ID_275130086 m1A Human chr6 - 44114211 44114211 44114211 ACAGACTGCAGACTTTTTTTTTTCCTCCCACCAGCACCACTGGGAGTCTGAGTGCGATTCAGAAG ACAGACTGCAGACTTTTTTTTTTCCTCCCACCGGCACCACTGGGAGTCTGAGTGCGATTCAGAAG T C MRPL14 Ensembl:ENSG00000180992 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr6:44114126..44114225;chr6:44114172..44116599 26863196,32194978 MeRIP-seq:(Medium) rs1562097077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1674026,Human_RBP_ID_23259167,Human_RBP_ID_26039257 RMVar_hsa_circ_77917,RMVar_hsa_circ_238733 76195 RMVar_ID_76195 Human_SNP_ID_275140930 m1A Human chr6 + 44155048 44155045 44155049 CTTGGGGGTTTCACTGCTCTCCCCCATGATGGAGGGAGGGAGCCCCCCAACCTCAGTGAGGAGAG CTTGGGGGTTTCACTGCTCTCCCCCATGAT____GGAGGGAGCCCCCCAACCTCAGTGAGGAGAG TGGAG T TMEM63B Ensembl:ENSG00000137216 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44154998..44155171 26863196 MeRIP-seq:(Medium) rs1239576867 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_665375,Human_RBP_ID_5122286,Human_RBP_ID_5151934,Human_RBP_ID_8216084,Human_RBP_ID_18171281,Human_RBP_ID_21991393,Human_RBP_ID_26539566 76196 RMVar_ID_76196 Human_SNP_ID_275140932 m1A Human chr6 + 44155048 44155048 44155048 CTTGGGGGTTTCACTGCTCTCCCCCATGATGGAGGGAGGGAGCCCCCCAACCTCAGTGAGGAGAG CTTGGGGGTTTCACTGCTCTCCCCCATGATGGGGGGAGGGAGCCCCCCAACCTCAGTGAGGAGAG A G TMEM63B Ensembl:ENSG00000137216 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44154998..44155171 26863196 MeRIP-seq:(Medium) rs921939222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665375,Human_RBP_ID_5122286,Human_RBP_ID_5151934,Human_RBP_ID_8216084,Human_RBP_ID_18171281,Human_RBP_ID_21991393,Human_RBP_ID_26539566 76197 RMVar_ID_76197 Human_SNP_ID_275140946 m1A Human chr6 + 44155070 44155070 44155070 CCCATGATGGAGGGAGGGAGCCCCCCAACCTCAGTGAGGAGAGCCCCGAGCCGGCCCCGGGGCAA CCCATGATGGAGGGAGGGAGCCCCCCAACCTCGGTGAGGAGAGCCCCGAGCCGGCCCCGGGGCAA A G TMEM63B Ensembl:ENSG00000137216 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44155019..44155221 32194978 MeRIP-seq:(Medium) rs1185336317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665375,Human_RBP_ID_5122286,Human_RBP_ID_5151934,Human_RBP_ID_8216084,Human_RBP_ID_18171281,Human_RBP_ID_21990840,Human_RBP_ID_26539566 76198 RMVar_ID_76198 Human_SNP_ID_275158198 m1A Human chr6 + 44219695 44219695 44219695 GCTCTCCAGCTGTGGCTATGGCCCCAGCCCCGAGATGAGGAGGGAGAGAACTAGGGGCCCGCAGG GCTCTCCAGCTGTGGCTATGGCCCCAGCCCCGTGATGAGGAGGGAGAGAACTAGGGGCCCGCAGG A T SLC29A1 Ensembl:ENSG00000112759 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:44219649..44219781 26863196 MeRIP-seq:(Medium) rs777372460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903376 Human_Splice_Rec_774447,Human_Splice_Rec_774473,Human_Splice_Rec_774497,Human_Splice_Rec_774521,Human_Splice_Rec_774531,Human_Splice_Rec_774537 76199 RMVar_ID_76199 Human_SNP_ID_275161877 m1A Human chr6 - 44232900 44232900 44232900 CCAGGCATCGTGCTCGAAGACCACAGTCAGGTAGCGGCGGGGCTTAATGTTGCACAGCAGCAGCA CCAGGCATCGTGCTCGAAGACCACAGTCAGGTGGCGGCGGGGCTTAATGTTGCACAGCAGCAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44232849..44232979 26863196 MeRIP-seq:(Medium) rs746487700 Functional Loss SNV dbSNP153 33..33 33 - - - 76200 RMVar_ID_76200 Human_SNP_ID_275161878 m1A Human chr6 - 44232900 44232900 44232900 CCAGGCATCGTGCTCGAAGACCACAGTCAGGTAGCGGCGGGGCTTAATGTTGCACAGCAGCAGCA CCAGGCATCGTGCTCGAAGACCACAGTCAGGTCGCGGCGGGGCTTAATGTTGCACAGCAGCAGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44232849..44232979 26863196 MeRIP-seq:(Medium) rs746487700 Functional Loss SNV dbSNP153 33..33 33 - - - 76201 RMVar_ID_76201 Human_SNP_ID_275165759 m1A Human chr6 + 44247157 44247157 44247157 TTGGGACTGTCTGGGTATCGGAAAGCAAGCCTACGTTGCTCACTATTACGTATAATCCTTTTCTT TTGGGACTGTCTGGGTATCGGAAAGCAAGCCTGCGTTGCTCACTATTACGTATAATCCTTTTCTT A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:44247101..44247219;chr6:44247101..44247509 26863196 MeRIP-seq:(Medium) rs1214864671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81300,Human_RBP_ID_671363,Human_RBP_ID_1218032,Human_RBP_ID_1674033,Human_RBP_ID_2022031,Human_RBP_ID_3008757,Human_RBP_ID_3810223,Human_RBP_ID_4892379,Human_RBP_ID_5478711,Human_RBP_ID_5511782,Human_RBP_ID_7609789,Human_RBP_ID_8645990,Human_RBP_ID_8901792,Human_RBP_ID_15836180,Human_RBP_ID_17307383,Human_RBP_ID_18866630,Human_RBP_ID_22831911,Human_RBP_ID_24164485,Human_RBP_ID_27098902,Human_RBP_ID_27525184,Human_RBP_ID_27756371 Human_Splice_Rec_774815,Human_Splice_Rec_774837 RMVar_hsa_circ_78775,RMVar_hsa_circ_238763 76202 RMVar_ID_76202 Human_SNP_ID_275165858 m1A Human chr6 - 44247344 44247328 44247344 GAAAACCGAGGAGGACTCAAAAAACCTCACCCACCACTACCCTCACCCTATAAAAATCCAGAGCG GAAAACCGAGGAGGACTCAAAAAACCTCACCC________________TATAAAAATCCAGAGCG AGGGTGAGGGTAGTGGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:44247342..44247515 26863196 MeRIP-seq:(Medium) rs1226180274 Functional Loss DEL dbSNP153 33..48 33 - - - 76203 RMVar_ID_76203 Human_SNP_ID_275166162 m1A Human chr6 - 44247980 44247977 44247981 ACAAAATTACAGAACAGGACCAAACCCAAGAAAGATGGTGGCCGTAGCCACCAGGCCGACACTCG ACAAAATTACAGAACAGGACCAAACCCAAGA____TGGTGGCCGTAGCCACCAGGCCGACACTCG ATCTT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:44247881..44248075 26863196 MeRIP-seq:(Medium) rs1015719166 Functional Loss DEL dbSNP153 32..35 33 - - - 76204 RMVar_ID_76204 Human_SNP_ID_275166163 m1A Human chr6 - 44247980 44247980 44247980 ACAAAATTACAGAACAGGACCAAACCCAAGAAAGATGGTGGCCGTAGCCACCAGGCCGACACTCG ACAAAATTACAGAACAGGACCAAACCCAAGAACGATGGTGGCCGTAGCCACCAGGCCGACACTCG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:44247881..44248075 26863196 MeRIP-seq:(Medium) rs1410338773 Functional Loss SNV dbSNP153 33..33 33 - - - 76205 RMVar_ID_76205 Human_SNP_ID_275166176 m1A Human chr6 + 44248020 44248020 44248020 GTTTGGTCCTGTTCTGTAATTTTGTGCTGTGAAAGGGTCGTGGTGGAGCTTTTGGCTTAAGAATT GTTTGGTCCTGTTCTGTAATTTTGTGCTGTGAGAGGGTCGTGGTGGAGCTTTTGGCTTAAGAATT A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:44247901..44248142 26863196 MeRIP-seq:(Medium) rs896652147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17162367,Human_RBP_ID_27842647 Human_Splice_Rec_774859 RMVar_hsa_circ_78775,RMVar_hsa_circ_238763 76206 RMVar_ID_76206 Human_SNP_ID_275166816 m1A Human chr6 - 44249725 44249725 44249725 ATCACAACCACTTTCTCTGCCACCAAGTAGGCAGAATAAAAGCCAACACCAAACTGCCCAATCAT ATCACAACCACTTTCTCTGCCACCAAGTAGGCTGAATAAAAGCCAACACCAAACTGCCCAATCAT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44249701..44249725 32194978 MeRIP-seq:(Medium) rs752909323 Functional Loss SNV dbSNP153 33..33 33 - - - 76207 RMVar_ID_76207 Human_SNP_ID_275166994 m1A Human chr6 - 44250152 44250152 44250152 AGTGTAAAAGATTTAAAAGTCCATACTCACATAAAGGGTGATGGGATAGCCTATGAACTGAGAAT AGTGTAAAAGATTTAAAAGTCCATACTCACATGAAGGGTGATGGGATAGCCTATGAACTGAGAAT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:44250126..44250175 26863196 MeRIP-seq:(Medium) rs1374546988 Functional Loss SNV dbSNP153 33..33 33 - - - 76208 RMVar_ID_76208 Human_SNP_ID_275167068 m1A Human chr6 + 44250355 44250331 44250355 TGATGAGGCAGAGGAAGAGAAAGGTGAGAAAGAAGAGGAAGATAAAGATGATGAAGAAAAACCCA TGATGAGGC________________________AGAGGAAGATAAAGATGATGAAGAAAAACCCA CAGAGGAAGAGAAAGGTGAGAAAGA C HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:44250276..44250475;chr6:44250271..44250556;chr6:44250269..44250557 26863196 MeRIP-seq:(Medium) rs753789449 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_79143,Human_RBP_ID_214900,Human_RBP_ID_665451,Human_RBP_ID_841789,Human_RBP_ID_1674063,Human_RBP_ID_2022052,Human_RBP_ID_7609845,Human_RBP_ID_10286304,Human_RBP_ID_18866656,Human_RBP_ID_23062558,Human_RBP_ID_23116428,Human_RBP_ID_24164502,Human_RBP_ID_24548400,Human_RBP_ID_26354039,Human_RBP_ID_27827713 Human_Splice_Rec_774802,Human_Splice_Rec_774824,Human_Splice_Rec_774846,Human_Splice_Rec_774868 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238769,RMVar_hsa_circ_91196,RMVar_hsa_circ_238768,RMVar_hsa_circ_22290,RMVar_hsa_circ_118483,RMVar_hsa_circ_238771,RMVar_hsa_circ_375698,RMVar_hsa_circ_55721,RMVar_hsa_circ_238772 76209 RMVar_ID_76209 Human_SNP_ID_275167112 m1A Human chr6 + 44250429 44250429 44250429 ATGTGGGTTCAGATGAGGAGGATGACAGCGGTAAGGATAAGAAGAAGAAAACTAAGAAGATCAAA ATGTGGGTTCAGATGAGGAGGATGACAGCGGTGAGGATAAGAAGAAGAAAACTAAGAAGATCAAA A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44250276..44250550 32194978 MeRIP-seq:(Medium) rs1252188086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79143,Human_RBP_ID_214902,Human_RBP_ID_251200,Human_RBP_ID_665452,Human_RBP_ID_841790,Human_RBP_ID_947761,Human_RBP_ID_1047899,Human_RBP_ID_1674066,Human_RBP_ID_2022055,Human_RBP_ID_3008782,Human_RBP_ID_3810241,Human_RBP_ID_7609850,Human_RBP_ID_8270185,Human_RBP_ID_8646013,Human_RBP_ID_8901807,Human_RBP_ID_9194860,Human_RBP_ID_9400616,Human_RBP_ID_15836318,Human_RBP_ID_17536380,Human_RBP_ID_17671993,Human_RBP_ID_18413856,Human_RBP_ID_18539131,Human_RBP_ID_18866657,Human_RBP_ID_19129471,Human_RBP_ID_22010805,Human_RBP_ID_22106854,Human_RBP_ID_22773666,Human_RBP_ID_23067586,Human_RBP_ID_23116467,Human_RBP_ID_24164505,Human_RBP_ID_24548403,Human_RBP_ID_26353199,Human_RBP_ID_27827715 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238769,RMVar_hsa_circ_91196,RMVar_hsa_circ_238768,RMVar_hsa_circ_22290,RMVar_hsa_circ_118483,RMVar_hsa_circ_238771,RMVar_hsa_circ_375698,RMVar_hsa_circ_55721,RMVar_hsa_circ_238772 76210 RMVar_ID_76210 Human_SNP_ID_275167159 m1A Human chr6 + 44250583 44250583 44250583 ATTCTACAAGAGCCTCACTAATGACTGGGAAGACCACTTGGCAGTCAAGGTGTGAGAAGCCTTTG ATTCTACAAGAGCCTCACTAATGACTGGGAAGGCCACTTGGCAGTCAAGGTGTGAGAAGCCTTTG A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1316131598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214620,Human_RBP_ID_251202,Human_RBP_ID_952190,Human_RBP_ID_1674069,Human_RBP_ID_2022057,Human_RBP_ID_3810243,Human_RBP_ID_7609856,Human_RBP_ID_8901809,Human_RBP_ID_9400625,Human_RBP_ID_15836325,Human_RBP_ID_17307389,Human_RBP_ID_18413857,Human_RBP_ID_18539137,Human_RBP_ID_19131318,Human_RBP_ID_24548408,Human_RBP_ID_26354052,Human_RBP_ID_27827723 Human_Splice_Rec_774803,Human_Splice_Rec_774825,Human_Splice_Rec_774847,Human_Splice_Rec_774869 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238769,RMVar_hsa_circ_91196,RMVar_hsa_circ_238768,RMVar_hsa_circ_22290,RMVar_hsa_circ_118483,RMVar_hsa_circ_238771,RMVar_hsa_circ_375698,RMVar_hsa_circ_55721,RMVar_hsa_circ_238772 76211 RMVar_ID_76211 Human_SNP_ID_275167755 m1A Human chr6 + 44252173 44252173 44252173 AGTTACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGAAGAAGAAGATGGAAGAGAGCA AGTTACCAAGGAGGGTCTGGAGCTGCCTGAGGGTGAGGAGGAGAAGAAGAAGATGGAAGAGAGCA A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:44252082..44252225 26863196 MeRIP-seq:(Medium) rs753862073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79151,Human_RBP_ID_214627,Human_RBP_ID_251204,Human_RBP_ID_665470,Human_RBP_ID_789708,Human_RBP_ID_841793,Human_RBP_ID_952162,Human_RBP_ID_1047911,Human_RBP_ID_1069761,Human_RBP_ID_1674092,Human_RBP_ID_2022071,Human_RBP_ID_3008806,Human_RBP_ID_3810253,Human_RBP_ID_4914477,Human_RBP_ID_5532500,Human_RBP_ID_7609882,Human_RBP_ID_8270189,Human_RBP_ID_8646035,Human_RBP_ID_8901821,Human_RBP_ID_9194870,Human_RBP_ID_9263014,Human_RBP_ID_9400648,Human_RBP_ID_9444299,Human_RBP_ID_15836364,Human_RBP_ID_17307394,Human_RBP_ID_17663316,Human_RBP_ID_18085438,Human_RBP_ID_18195613,Human_RBP_ID_18539139,Human_RBP_ID_18866681,Human_RBP_ID_22105199,Human_RBP_ID_22462119,Human_RBP_ID_22514422,Human_RBP_ID_22773671,Human_RBP_ID_23067849,Human_RBP_ID_23139069,Human_RBP_ID_24164522,Human_RBP_ID_24548409,Human_RBP_ID_26353208,Human_RBP_ID_27525222,Human_RBP_ID_27756388,Human_RBP_ID_27827725 Human_Splice_Rec_774811,Human_Splice_Rec_774833,Human_Splice_Rec_774855,Human_Splice_Rec_774877 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238768,RMVar_hsa_circ_118483,RMVar_hsa_circ_238772,RMVar_hsa_circ_98386,RMVar_hsa_circ_117331,RMVar_hsa_circ_126675,RMVar_hsa_circ_238774,RMVar_hsa_circ_238775,RMVar_hsa_circ_238776,RMVar_hsa_circ_81404,RMVar_hsa_circ_238777 76212 RMVar_ID_76212 Human_SNP_ID_275167756 m1A Human chr6 + 44252176 44252174 44252177 TACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGAAGAAGAAGATGGAAGAGAGCAAGG TACCAAGGAGGGTCTGGAGCTGCCTGAGGAT___GAGGAGAAGAAGAAGATGGAAGAGAGCAAGG TGAG T HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA heat shock 4h chr6:44251932..44252300 31548705,26863196 m1A-IP-seq:(High) rs763616071 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_79151,Human_RBP_ID_214627,Human_RBP_ID_251204,Human_RBP_ID_665470,Human_RBP_ID_789708,Human_RBP_ID_841793,Human_RBP_ID_952162,Human_RBP_ID_1069761,Human_RBP_ID_1674092,Human_RBP_ID_2022071,Human_RBP_ID_3008806,Human_RBP_ID_3810253,Human_RBP_ID_4914477,Human_RBP_ID_5532500,Human_RBP_ID_7609882,Human_RBP_ID_8270189,Human_RBP_ID_8646035,Human_RBP_ID_8901821,Human_RBP_ID_9194870,Human_RBP_ID_9263014,Human_RBP_ID_9400648,Human_RBP_ID_9444299,Human_RBP_ID_15836364,Human_RBP_ID_17663316,Human_RBP_ID_18085438,Human_RBP_ID_18195613,Human_RBP_ID_18539139,Human_RBP_ID_18866681,Human_RBP_ID_22105199,Human_RBP_ID_22462119,Human_RBP_ID_22514422,Human_RBP_ID_22773671,Human_RBP_ID_23067849,Human_RBP_ID_23139069,Human_RBP_ID_24164522,Human_RBP_ID_24548409,Human_RBP_ID_26353208,Human_RBP_ID_27525222,Human_RBP_ID_27756388,Human_RBP_ID_27827725 Human_Splice_Rec_774811,Human_Splice_Rec_774833,Human_Splice_Rec_774855,Human_Splice_Rec_774877 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238768,RMVar_hsa_circ_118483,RMVar_hsa_circ_238772,RMVar_hsa_circ_98386,RMVar_hsa_circ_117331,RMVar_hsa_circ_126675,RMVar_hsa_circ_238774,RMVar_hsa_circ_238775,RMVar_hsa_circ_238776,RMVar_hsa_circ_81404,RMVar_hsa_circ_238777 76213 RMVar_ID_76213 Human_SNP_ID_275167757 m1A Human chr6 - 44252174 44252174 44252174 TTGCTCTCTTCCATCTTCTTCTTCTCCTCCTCATCCTCAGGCAGCTCCAGACCCTCCTTGGTAAC TTGCTCTCTTCCATCTTCTTCTTCTCCTCCTCCTCCTCAGGCAGCTCCAGACCCTCCTTGGTAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44252046..44252230 26863196 MeRIP-seq:(Medium) rs1561901111 Functional Loss SNV dbSNP153 33..33 33 - - - 76214 RMVar_ID_76214 Human_SNP_ID_275167758 m1A Human chr6 + 44252176 44252176 44252176 TACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGAAGAAGAAGATGGAAGAGAGCAAGG TACCAAGGAGGGTCTGGAGCTGCCTGAGGATGGGGAGGAGAAGAAGAAGATGGAAGAGAGCAAGG A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA heat shock 4h chr6:44251932..44252300 31548705,26863196 m1A-IP-seq:(High) rs754953829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79151,Human_RBP_ID_214627,Human_RBP_ID_251204,Human_RBP_ID_665470,Human_RBP_ID_789708,Human_RBP_ID_841793,Human_RBP_ID_952162,Human_RBP_ID_1069761,Human_RBP_ID_1674092,Human_RBP_ID_2022071,Human_RBP_ID_3008806,Human_RBP_ID_3810253,Human_RBP_ID_4914477,Human_RBP_ID_5532500,Human_RBP_ID_7609882,Human_RBP_ID_8270189,Human_RBP_ID_8646035,Human_RBP_ID_8901821,Human_RBP_ID_9194870,Human_RBP_ID_9263014,Human_RBP_ID_9400648,Human_RBP_ID_9444299,Human_RBP_ID_15836364,Human_RBP_ID_17663316,Human_RBP_ID_18085438,Human_RBP_ID_18195613,Human_RBP_ID_18539139,Human_RBP_ID_18866681,Human_RBP_ID_22105199,Human_RBP_ID_22462119,Human_RBP_ID_22514422,Human_RBP_ID_22773671,Human_RBP_ID_23067849,Human_RBP_ID_23139069,Human_RBP_ID_24164522,Human_RBP_ID_24548409,Human_RBP_ID_26353208,Human_RBP_ID_27525222,Human_RBP_ID_27756388,Human_RBP_ID_27827725 Human_Splice_Rec_774811,Human_Splice_Rec_774833,Human_Splice_Rec_774855,Human_Splice_Rec_774877 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238768,RMVar_hsa_circ_118483,RMVar_hsa_circ_238772,RMVar_hsa_circ_98386,RMVar_hsa_circ_117331,RMVar_hsa_circ_126675,RMVar_hsa_circ_238774,RMVar_hsa_circ_238775,RMVar_hsa_circ_238776,RMVar_hsa_circ_81404,RMVar_hsa_circ_238777 76215 RMVar_ID_76215 Human_SNP_ID_275167759 m1A Human chr6 + 44252176 44252176 44252176 TACCAAGGAGGGTCTGGAGCTGCCTGAGGATGAGGAGGAGAAGAAGAAGATGGAAGAGAGCAAGG TACCAAGGAGGGTCTGGAGCTGCCTGAGGATGTGGAGGAGAAGAAGAAGATGGAAGAGAGCAAGG A T HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA heat shock 4h chr6:44251932..44252300 31548705,26863196 m1A-IP-seq:(High) rs754953829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79151,Human_RBP_ID_214627,Human_RBP_ID_251204,Human_RBP_ID_665470,Human_RBP_ID_789708,Human_RBP_ID_841793,Human_RBP_ID_952162,Human_RBP_ID_1069761,Human_RBP_ID_1674092,Human_RBP_ID_2022071,Human_RBP_ID_3008806,Human_RBP_ID_3810253,Human_RBP_ID_4914477,Human_RBP_ID_5532500,Human_RBP_ID_7609882,Human_RBP_ID_8270189,Human_RBP_ID_8646035,Human_RBP_ID_8901821,Human_RBP_ID_9194870,Human_RBP_ID_9263014,Human_RBP_ID_9400648,Human_RBP_ID_9444299,Human_RBP_ID_15836364,Human_RBP_ID_17663316,Human_RBP_ID_18085438,Human_RBP_ID_18195613,Human_RBP_ID_18539139,Human_RBP_ID_18866681,Human_RBP_ID_22105199,Human_RBP_ID_22462119,Human_RBP_ID_22514422,Human_RBP_ID_22773671,Human_RBP_ID_23067849,Human_RBP_ID_23139069,Human_RBP_ID_24164522,Human_RBP_ID_24548409,Human_RBP_ID_26353208,Human_RBP_ID_27525222,Human_RBP_ID_27756388,Human_RBP_ID_27827725 Human_Splice_Rec_774811,Human_Splice_Rec_774833,Human_Splice_Rec_774855,Human_Splice_Rec_774877 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238768,RMVar_hsa_circ_118483,RMVar_hsa_circ_238772,RMVar_hsa_circ_98386,RMVar_hsa_circ_117331,RMVar_hsa_circ_126675,RMVar_hsa_circ_238774,RMVar_hsa_circ_238775,RMVar_hsa_circ_238776,RMVar_hsa_circ_81404,RMVar_hsa_circ_238777 76216 RMVar_ID_76216 Human_SNP_ID_275168217 m1A Human chr6 - 44253118 44253118 44253118 CCCGAAGTGCCTGGGCTTTCATGATCCGCTCCATATTGGCTGTCCAGCCGTAGGTGCTGGTCACA CCCGAAGTGCCTGGGCTTTCATGATCCGCTCCGTATTGGCTGTCCAGCCGTAGGTGCTGGTCACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:44253093..44253250 26863196 MeRIP-seq:(Medium) rs1346744944 Functional Loss SNV dbSNP153 33..33 33 - - - 76217 RMVar_ID_76217 Human_SNP_ID_275168238 m1A Human chr6 - 44253203 44253203 44253203 TTCTGCCGCAGCGTCTCCACAATGGGGTGGTCAGGGTTGATCTCCAGGTGCTTTTTGGCCATCAT TTCTGCCGCAGCGTCTCCACAATGGGGTGGTCGGGGTTGATCTCCAGGTGCTTTTTGGCCATCAT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:44253081..44253325 26863196 MeRIP-seq:(Medium) rs61753593 Functional Loss SNV dbSNP153 33..33 33 - - - 76218 RMVar_ID_76218 Human_SNP_ID_275168429 m1A Human chr6 + 44253585 44253585 44253585 TCTCGAGGGCGATGAGGATGCGTCTCGCATGGAAGAAGTCGATTAGGTTAGGAGTTCATAGTTGG TCTCGAGGGCGATGAGGATGCGTCTCGCATGGGAGAAGTCGATTAGGTTAGGAGTTCATAGTTGG A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44253535..44253749 26863196 MeRIP-seq:(Medium) rs1247230018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_285196,Human_RBP_ID_665482,Human_RBP_ID_1113259,Human_RBP_ID_1674109,Human_RBP_ID_2022084,Human_RBP_ID_3008822,Human_RBP_ID_3810264,Human_RBP_ID_4892461,Human_RBP_ID_7609906,Human_RBP_ID_8646055,Human_RBP_ID_8901830,Human_RBP_ID_9194878,Human_RBP_ID_15836410,Human_RBP_ID_18866700,Human_RBP_ID_21221961,Human_RBP_ID_22831955,Human_RBP_ID_23062591,Human_RBP_ID_24164535,Human_RBP_ID_26541290,Human_RBP_ID_27098969,Human_RBP_ID_27347935 Human_Splice_Rec_774814,Human_Splice_Rec_774836,Human_Splice_Rec_774858,Human_Splice_Rec_774880 Human_miRNA_ID_2896365 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_238765,RMVar_hsa_circ_238768,RMVar_hsa_circ_76342,RMVar_hsa_circ_118483,RMVar_hsa_circ_238772,RMVar_hsa_circ_98386,RMVar_hsa_circ_238776,RMVar_hsa_circ_81404,RMVar_hsa_circ_238777,RMVar_hsa_circ_238778 76219 RMVar_ID_76219 Human_SNP_ID_275168463 m1A Human chr6 - 44253634 44253633 44253635 GAGGCTGCAGTGGGAGCCCATGGGGACACTATACAAGGGCACAAGTTTTCCAACTATGAACTCCT GAGGCTGCAGTGGGAGCCCATGGGGACACTA__CAAGGGCACAAGTTTTCCAACTATGAACTCCT GTA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44253476..44253775 32194978 MeRIP-seq:(Medium) rs1250586407 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18077514 76220 RMVar_ID_76220 Human_SNP_ID_275168464 m1A Human chr6 - 44253634 44253634 44253634 GAGGCTGCAGTGGGAGCCCATGGGGACACTATACAAGGGCACAAGTTTTCCAACTATGAACTCCT GAGGCTGCAGTGGGAGCCCATGGGGACACTATGCAAGGGCACAAGTTTTCCAACTATGAACTCCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44253476..44253775 32194978 MeRIP-seq:(Medium) rs1453780093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18077514 76221 RMVar_ID_76221 Human_SNP_ID_275168493 m1A Human chr6 - 44253676 44253674 44253676 ACTAGACACCAGCAGGGGGAGCCAGGTGGGACAGGGGCACTCGAGGCTGCAGTGGGAGCCCATGG ACTAGACACCAGCAGGGGGAGCCAGGTGGGAC__GGGCACTCGAGGCTGCAGTGGGAGCCCATGG CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44253459..44253775 26863196 MeRIP-seq:(Medium) rs1430917000 Functional Loss DEL dbSNP153 33..34 33 - - - 76222 RMVar_ID_76222 Human_SNP_ID_275168495 m1A Human chr6 - 44253676 44253675 44253676 ACTAGACACCAGCAGGGGGAGCCAGGTGGGACAGGGGCACTCGAGGCTGCAGTGGGAGCCCATGG ACTAGACACCAGCAGGGGGAGCCAGGTGGGAC_GGGGCACTCGAGGCTGCAGTGGGAGCCCATGG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44253459..44253775 26863196 MeRIP-seq:(Medium) rs775657325 Functional Loss DEL dbSNP153 33..33 33 - - - 76223 RMVar_ID_76223 Human_SNP_ID_275168496 m1A Human chr6 - 44253676 44253676 44253676 ACTAGACACCAGCAGGGGGAGCCAGGTGGGACAGGGGCACTCGAGGCTGCAGTGGGAGCCCATGG ACTAGACACCAGCAGGGGGAGCCAGGTGGGACGGGGGCACTCGAGGCTGCAGTGGGAGCCCATGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44253459..44253775 26863196 MeRIP-seq:(Medium) rs1175123533 Functional Loss SNV dbSNP153 33..33 33 - - - 76224 RMVar_ID_76224 Human_SNP_ID_275168521 m1A Human chr6 - 44253701 44253701 44253701 ACAAGGACAGGAGAGGGAAAAAAACACTAGACACCAGCAGGGGGAGCCAGGTGGGACAGGGGCAC ACAAGGACAGGAGAGGGAAAAAAACACTAGACGCCAGCAGGGGGAGCCAGGTGGGACAGGGGCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44253651..44253775 32194978 MeRIP-seq:(Medium) rs1260148973 Functional Loss SNV dbSNP153 33..33 33 - - - 76225 RMVar_ID_76225 Human_SNP_ID_275169006 m1A Human chr6 + 44254721 44254721 44254721 TCAGGCCCTTTCCACCCTCAAACCTTCTGCACAGGAGACTCAACAGGCACAGCCTTCTTTCCCCG TCAGGCCCTTTCCACCCTCAAACCTTCTGCACCGGAGACTCAACAGGCACAGCCTTCTTTCCCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44254672..44254822 26863196 MeRIP-seq:(Medium) rs528603457 Functional Loss SNV dbSNP153 33..33 33 - - - 76226 RMVar_ID_76226 Human_SNP_ID_275169007 m1A Human chr6 + 44254721 44254721 44254721 TCAGGCCCTTTCCACCCTCAAACCTTCTGCACAGGAGACTCAACAGGCACAGCCTTCTTTCCCCG TCAGGCCCTTTCCACCCTCAAACCTTCTGCACGGGAGACTCAACAGGCACAGCCTTCTTTCCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44254672..44254822 26863196 MeRIP-seq:(Medium) rs528603457 Functional Loss SNV dbSNP153 33..33 33 - - - 76227 RMVar_ID_76227 Human_SNP_ID_275169300 m1A Human chr6 - 44255206 44255206 44255206 CCAGCGGACCAGAGCCCCGCAGCTCCCCAGCCACCACACTCTCAGGCCTCATCTTACTGGCAGGT CCAGCGGACCAGAGCCCCGCAGCTCCCCAGCCCCCACACTCTCAGGCCTCATCTTACTGGCAGGT T G SLC35B2 Ensembl:ENSG00000157593 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44255158..44255325 26863196 MeRIP-seq:(Medium) rs1477163242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17422131,Human_RBP_ID_27347950,Human_RBP_ID_27525253 Human_miRNA_ID_2909967 RMVar_hsa_circ_85787,RMVar_hsa_circ_238779 76228 RMVar_ID_76228 Human_SNP_ID_275169326 m1A Human chr6 - 44255251 44255251 44255251 TGACAGCCACCCTCATCTCCATTGGGGTCAGCATGTTTCTGCTATCCAGCGGACCAGAGCCCCGC TGACAGCCACCCTCATCTCCATTGGGGTCAGCGTGTTTCTGCTATCCAGCGGACCAGAGCCCCGC T C SLC35B2 Ensembl:ENSG00000157593 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44255201..44255250 32194978 MeRIP-seq:(Medium) rs546237790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665521,Human_RBP_ID_4892509,Human_RBP_ID_24164551,Human_RBP_ID_27347951,Human_RBP_ID_27527075 Human_miRNA_ID_1999803,Human_miRNA_ID_2731194,Human_miRNA_ID_2948774 RMVar_hsa_circ_85787,RMVar_hsa_circ_238779 76229 RMVar_ID_76229 Human_SNP_ID_275169337 m1A Human chr6 - 44255263 44255263 44255263 ACTGGGAGTACCTGACAGCCACCCTCATCTCCATTGGGGTCAGCATGTTTCTGCTATCCAGCGGA ACTGGGAGTACCTGACAGCCACCCTCATCTCCGTTGGGGTCAGCATGTTTCTGCTATCCAGCGGA T C SLC35B2 Ensembl:ENSG00000157593 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44255213..44255324 26863196 MeRIP-seq:(Medium) rs1380780173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665521,Human_RBP_ID_8646077,Human_RBP_ID_15836440,Human_RBP_ID_27347951,Human_RBP_ID_27525256 Human_miRNA_ID_2731194,Human_miRNA_ID_2948774 RMVar_hsa_circ_85787,RMVar_hsa_circ_238779 76230 RMVar_ID_76230 Human_SNP_ID_275169805 m1A Human chr6 - 44256544 44256541 44256544 AGCAGGGCAGGCTGGCTGCTCTGGGGAAGATGAAGTGCTATGGAGAAGATTTGGGGCTTGACTTT AGCAGGGCAGGCTGGCTGCTCTGGGGAAGATG___TGCTATGGAGAAGATTTGGGGCTTGACTTT ACTT A SLC35B2 Ensembl:ENSG00000157593 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44256524..44256678 26863196 MeRIP-seq:(Medium) rs1309218358 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5398944,Human_RBP_ID_8646084,Human_RBP_ID_9438168,Human_RBP_ID_22684916 76231 RMVar_ID_76231 Human_SNP_ID_275170162 m1A Human chr6 + 44257495 44257495 44257495 CGCGCGCCCCCTGCGCTCCCGCCGCCGCCTCCAGGAGCGGCCAGCGAGCCAGCGGCCAGCGGAAG CGCGCGCCCCCTGCGCTCCCGCCGCCGCCTCCGGGAGCGGCCAGCGAGCCAGCGGCCAGCGGAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:44257180..44257525 26863196 MeRIP-seq:(Medium) rs960534984 Functional Loss SNV dbSNP153 33..33 33 - - - 76232 RMVar_ID_76232 Human_SNP_ID_275181450 m1A Human chr6 - 44299092 44299092 44299092 GAAATCAGGGAAAAGCATTCCAGCCTGAGGGAACAGCCAATGCAGAGGCCGTGAGGTGGCCAGTG GAAATCAGGGAAAAGCATTCCAGCCTGAGGGACCAGCCAATGCAGAGGCCGTGAGGTGGCCAGTG T G AARS2 Ensembl:ENSG00000124608 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:44299045..44299242 26863196 MeRIP-seq:(Medium) rs1284187153 Functional Loss SNV dbSNP153 33..33 33 - - - 76233 RMVar_ID_76233 Human_SNP_ID_275181905 m1A Human chr6 - 44300648 44300648 44300648 GGGCACTGGCAGTGTGCAGCCACATGGGGGGCAAGGCGTGGGGCTCACGAGTGGTGGCCCAAGGC GGGCACTGGCAGTGTGCAGCCACATGGGGGGCGAGGCGTGGGGCTCACGAGTGGTGGCCCAAGGC T C AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44300602..44300753 32194978 MeRIP-seq:(Medium) rs1451561432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532503,Human_RBP_ID_22618562,Human_RBP_ID_22728199 Human_Splice_Rec_775014 76234 RMVar_ID_76234 Human_SNP_ID_275182346 m1A Human chr6 - 44302119 44302119 44302119 TGCCCCAGTGGCAGCGGCGGGAGCTGCTGGCCACAGTGAAGATGCTGCAGCGGCGTGCCAACACT TGCCCCAGTGGCAGCGGCGGGAGCTGCTGGCCGCAGTGAAGATGCTGCAGCGGCGTGCCAACACT T C AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44301152..44303075 32194978 MeRIP-seq:(Medium) rs200928541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949738,Human_RBP_ID_23067850 Human_Splice_Rec_775008,Human_Splice_Rec_775009 Human_miRNA_ID_1936802,Human_miRNA_ID_1947902 RMVar_hsa_circ_78648,RMVar_hsa_circ_118573,RMVar_hsa_circ_238785,RMVar_hsa_circ_328848,RMVar_hsa_circ_238786 76235 RMVar_ID_76235 Human_SNP_ID_275182347 m1A Human chr6 - 44302119 44302119 44302119 TGCCCCAGTGGCAGCGGCGGGAGCTGCTGGCCACAGTGAAGATGCTGCAGCGGCGTGCCAACACT TGCCCCAGTGGCAGCGGCGGGAGCTGCTGGCCCCAGTGAAGATGCTGCAGCGGCGTGCCAACACT T G AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:44301152..44303075 32194978 MeRIP-seq:(Medium) rs200928541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949738,Human_RBP_ID_23067850 Human_Splice_Rec_775008,Human_Splice_Rec_775009 Human_miRNA_ID_1936802,Human_miRNA_ID_1947902 RMVar_hsa_circ_78648,RMVar_hsa_circ_118573,RMVar_hsa_circ_238785,RMVar_hsa_circ_328848,RMVar_hsa_circ_238786 76236 RMVar_ID_76236 Human_SNP_ID_275182803 m1A Human chr6 - 44303345 44303345 44303345 AGGAGGCCGTGGGGCAGGATGAGGCTGTGTACATGGAGGAGGTGCCCCTGGCGCTCACTGCCCAG AGGAGGCCGTGGGGCAGGATGAGGCTGTGTACTTGGAGGAGGTGCCCCTGGCGCTCACTGCCCAG T A AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:44303284..44303370 26863196 MeRIP-seq:(Medium) rs955369277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4914535,Human_RBP_ID_7609986,Human_RBP_ID_21347228,Human_RBP_ID_23120368 Human_Splice_Rec_775000,Human_Splice_Rec_775001 RMVar_hsa_circ_37685,RMVar_hsa_circ_78648,RMVar_hsa_circ_104129,RMVar_hsa_circ_118573,RMVar_hsa_circ_238785,RMVar_hsa_circ_238786,RMVar_hsa_circ_125153,RMVar_hsa_circ_238787,RMVar_hsa_circ_96862,RMVar_hsa_circ_238788,RMVar_hsa_circ_238789 76237 RMVar_ID_76237 Human_SNP_ID_275182804 m1A Human chr6 - 44303345 44303345 44303345 AGGAGGCCGTGGGGCAGGATGAGGCTGTGTACATGGAGGAGGTGCCCCTGGCGCTCACTGCCCAG AGGAGGCCGTGGGGCAGGATGAGGCTGTGTACGTGGAGGAGGTGCCCCTGGCGCTCACTGCCCAG T C AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:44303284..44303370 26863196 MeRIP-seq:(Medium) rs955369277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4914535,Human_RBP_ID_7609986,Human_RBP_ID_21347228,Human_RBP_ID_23120368 Human_Splice_Rec_775000,Human_Splice_Rec_775001 RMVar_hsa_circ_37685,RMVar_hsa_circ_78648,RMVar_hsa_circ_104129,RMVar_hsa_circ_118573,RMVar_hsa_circ_238785,RMVar_hsa_circ_238786,RMVar_hsa_circ_125153,RMVar_hsa_circ_238787,RMVar_hsa_circ_96862,RMVar_hsa_circ_238788,RMVar_hsa_circ_238789 76238 RMVar_ID_76238 Human_SNP_ID_275183451 m1A Human chr6 - 44305125 44305125 44305125 GTGGCTTGATGTCCATGCGCTTGGGGAGCTGCAGCGCCAAGGAGTGCCCCCAACTGACGACAGCC GTGGCTTGATGTCCATGCGCTTGGGGAGCTGCGGCGCCAAGGAGTGCCCCCAACTGACGACAGCC T C AARS2 Ensembl:ENSG00000124608 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44305035..44305152 26863196 MeRIP-seq:(Medium) rs754462031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949744,Human_RBP_ID_26354074 Human_Splice_Rec_774992,Human_Splice_Rec_774993 Human_miRNA_ID_2012131,Human_miRNA_ID_2217340,Human_miRNA_ID_2708153,Human_miRNA_ID_2758497 RMVar_hsa_circ_78648,RMVar_hsa_circ_104129,RMVar_hsa_circ_118573,RMVar_hsa_circ_238785,RMVar_hsa_circ_238786,RMVar_hsa_circ_125153,RMVar_hsa_circ_238787,RMVar_hsa_circ_81651,RMVar_hsa_circ_96862,RMVar_hsa_circ_238788,RMVar_hsa_circ_124693,RMVar_hsa_circ_238789,RMVar_hsa_circ_117474,RMVar_hsa_circ_238790,RMVar_hsa_circ_238791,RMVar_hsa_circ_126920,RMVar_hsa_circ_238792,RMVar_hsa_circ_238794,RMVar_hsa_circ_92010,RMVar_hsa_circ_238793,RMVar_hsa_circ_127580,RMVar_hsa_circ_238795 76239 RMVar_ID_76239 Human_SNP_ID_275203770 m1A Human chr6 + 44390144 44390143 44390144 TAATGAGGTTTTCATCCTTAGTCTTTTAACCTAGGTGGTGTGTATGTGCATGTTATATGTCTCTT TAATGAGGTTTTCATCCTTAGTCTTTTAACCT_GGTGGTGTGTATGTGCATGTTATATGTCTCTT TA T CDC5L Ensembl:ENSG00000096401 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:44390108..44390235 26863196 MeRIP-seq:(Medium) rs1215346550 Functional Loss DEL dbSNP153 33..33 33 - - - 76240 RMVar_ID_76240 Human_SNP_ID_275213324 m1A Human chr6 + 44429815 44429815 44429815 AAGCTTATAACCAGGTGTGGGAAGAATGCTACAGTCAAGTTTTATATCTTCCTGGGCAGAGCCGC AAGCTTATAACCAGGTGTGGGAAGAATGCTACCGTCAAGTTTTATATCTTCCTGGGCAGAGCCGC A C CDC5L Ensembl:ENSG00000096401 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44426673..44445655 32194978 MeRIP-seq:(Medium) rs769155730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1327778,Human_RBP_ID_2022185,Human_RBP_ID_3810334,Human_RBP_ID_7610242,Human_RBP_ID_8237371,Human_RBP_ID_18866829,Human_RBP_ID_24164674,Human_RBP_ID_27828659 Human_Splice_Rec_775111 Human_miRNA_ID_858516 RMVar_hsa_circ_358389,RMVar_hsa_circ_238810,RMVar_hsa_circ_320478,RMVar_hsa_circ_347218,RMVar_hsa_circ_377549 76241 RMVar_ID_76241 Human_SNP_ID_275217233 m1A Human chr6 + 44446741 44446733 44446741 TGAAGTACAGTTTATATTCTGTCACAGGATTAATTAATTGCCGGTTTTCATACTCTAGAAGGCTG TGAAGTACAGTTTATATTCTGTCAC________TTAATTGCCGGTTTTCATACTCTAGAAGGCTG CAGGATTAA C CDC5L Ensembl:ENSG00000096401 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44446691..44446842 32194978 MeRIP-seq:(Medium) rs1419664179 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_1047948,Human_RBP_ID_1674217,Human_RBP_ID_2022203,Human_RBP_ID_3810349,Human_RBP_ID_4892766,Human_RBP_ID_7610370,Human_RBP_ID_8141833,Human_RBP_ID_8646148,Human_RBP_ID_8901899,Human_RBP_ID_17307414,Human_RBP_ID_17536400,Human_RBP_ID_18077594,Human_RBP_ID_18371685,Human_RBP_ID_27099104,Human_RBP_ID_27756422 76242 RMVar_ID_76242 Human_SNP_ID_45023911 m1A Human chr1 - 197146343 197146340 197146343 CGCGGGGCTGCGGGGCCCCGCGGCCGAGGAGGAGGCGTCTTCCCCGCCGGTCCTGTCTCTCAGCC CGCGGGGCTGCGGGGCCCCGCGGCCGAGGAGG___CGTCTTCCCCGCCGGTCCTGTCTCTCAGCC GCCT G ASPM Ensembl:ENSG00000066279 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:197146294..197146594 26863196 MeRIP-seq:(Medium) rs774902202 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_221132,Human_RBP_ID_22871016 Human_miRNA_ID_2145966,Human_miRNA_ID_2987400,Human_miRNA_ID_3021091,Human_miRNA_ID_3056684 RMVar_hsa_circ_78214,RMVar_hsa_circ_138601 76243 RMVar_ID_76243 Human_SNP_ID_45023913 m1A Human chr1 - 197146343 197146343 197146343 CGCGGGGCTGCGGGGCCCCGCGGCCGAGGAGGAGGCGTCTTCCCCGCCGGTCCTGTCTCTCAGCC CGCGGGGCTGCGGGGCCCCGCGGCCGAGGAGGGGGCGTCTTCCCCGCCGGTCCTGTCTCTCAGCC T C ASPM Ensembl:ENSG00000066279 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:197146294..197146594 26863196 MeRIP-seq:(Medium) rs903793902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221132,Human_RBP_ID_22871016 Human_miRNA_ID_2145966,Human_miRNA_ID_2987400,Human_miRNA_ID_3021091,Human_miRNA_ID_3056684 RMVar_hsa_circ_78214,RMVar_hsa_circ_138601 76244 RMVar_ID_76244 Human_SNP_ID_45023971 m1A Human chr1 + 197146421 197146421 197146421 CGGTCGGGCTCACTTCCCAGCAGCCTCGCCCCACTCGCCGGTTCGCCATGGCAGATTCGAGACCC CGGTCGGGCTCACTTCCCAGCAGCCTCGCCCCGCTCGCCGGTTCGCCATGGCAGATTCGAGACCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:197146376..197146525 26863196 MeRIP-seq:(Medium) rs886045779 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_349 76245 RMVar_ID_76245 Human_SNP_ID_45023982 m1A Human chr1 + 197146436 197146436 197146436 CCCAGCAGCCTCGCCCCACTCGCCGGTTCGCCATGGCAGATTCGAGACCCCTCCTGGATCTCCTT CCCAGCAGCCTCGCCCCACTCGCCGGTTCGCCGTGGCAGATTCGAGACCCCTCCTGGATCTCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:197146389..197146616 26863196 MeRIP-seq:(Medium) rs761447719 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_350 76246 RMVar_ID_76246 Human_SNP_ID_45024016 m1A Human chr1 + 197146495 197146495 197146495 CTCCTTGCCCCGCTCCCACGAGGCGGCTCCGGAGCGGGGATCCGGGACTTACGCTGACCGCTTCC CTCCTTGCCCCGCTCCCACGAGGCGGCTCCGGTGCGGGGATCCGGGACTTACGCTGACCGCTTCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:197146448..197146636 26863196 MeRIP-seq:(Medium) rs1030985769 Functional Loss SNV dbSNP153 33..33 33 - - - 76247 RMVar_ID_76247 Human_SNP_ID_45073299 m1A Human chr1 + 197354825 197354812 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCC_____________CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCCCGCCCCCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1256228767 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76248 RMVar_ID_76248 Human_SNP_ID_45073300 m1A Human chr1 + 197354825 197354813 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCC____________CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCCGCCCCCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1483995307 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76249 RMVar_ID_76249 Human_SNP_ID_45073307 m1A Human chr1 + 197354825 197354816 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCC_________CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CGCCCCCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1558076211 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76250 RMVar_ID_76250 Human_SNP_ID_45073313 m1A Human chr1 + 197354825 197354817 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCG________CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC GCCCCCCCA G CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1558076228 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76251 RMVar_ID_76251 Human_SNP_ID_45073319 m1A Human chr1 + 197354825 197354818 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGC_______CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCCCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1198253772 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76252 RMVar_ID_76252 Human_SNP_ID_45073322 m1A Human chr1 + 197354825 197354820 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCC_____CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1241943499 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76253 RMVar_ID_76253 Human_SNP_ID_45073325 m1A Human chr1 + 197354825 197354821 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCCC____CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1558076262 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76254 RMVar_ID_76254 Human_SNP_ID_45073328 m1A Human chr1 + 197354825 197354822 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCCCC___CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1458198200 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76255 RMVar_ID_76255 Human_SNP_ID_45073330 m1A Human chr1 + 197354825 197354823 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCCCCC__CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CCA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1180417673 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76256 RMVar_ID_76256 Human_SNP_ID_45073333 m1A Human chr1 + 197354825 197354824 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCCCCCC_CCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CA C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs372140447 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76257 RMVar_ID_76257 Human_SNP_ID_45073336 m1A Human chr1 + 197354825 197354825 197354825 CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCACCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC CTTTTATTCCCTTATCTGCCCCCCGCCCCCCCCCCCCCCCCCCCCGCCCACCCCCCCCCCCCCGC A C CRB1 Ensembl:ENSG00000134376 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:197354813..197354888;chr1:197354801..197354944;chr1:197354801..197354947;chr1:197354811..197354895 26863196 MeRIP-seq:(Medium) rs1417531871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17214647 RMVar_hsa_circ_328980,RMVar_hsa_circ_42569,RMVar_hsa_circ_6329,RMVar_hsa_circ_138621,RMVar_hsa_circ_138622,RMVar_hsa_circ_303478,RMVar_hsa_circ_138623 76258 RMVar_ID_76258 Human_SNP_ID_45173808 m1A Human chr1 + 197775306 197775306 197775306 AGGCTGCTCACAGCAGCCGTGGCGGCGGGCCCATGTCGGCTGCGCCCCCGGCACTTCCCCGCCTC AGGCTGCTCACAGCAGCCGTGGCGGCGGGCCCCTGTCGGCTGCGCCCCCGGCACTTCCCCGCCTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:197775232..197775434 26863196 MeRIP-seq:(Medium) rs1000797646 Functional Loss SNV dbSNP153 33..33 33 - - - 76259 RMVar_ID_76259 Human_SNP_ID_45173831 m1A Human chr1 - 197775361 197775361 197775361 GGGCGGCGGCCACGCCACCGCTGCTGTCACAGAAAGGCTCTGGTGGGTGGGGTGGGAGGCGGGGA GGGCGGCGGCCACGCCACCGCTGCTGTCACAGGAAGGCTCTGGTGGGTGGGGTGGGAGGCGGGGA T C DENND1B Ensembl:ENSG00000213047 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:197775312..197775437 26863196 MeRIP-seq:(Medium) rs900561148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4076268 Human_Splice_Rec_170017 RMVar_hsa_circ_75870,RMVar_hsa_circ_138654 76260 RMVar_ID_76260 Human_SNP_ID_45205116 m1A Human chr1 - 197902727 197902727 197902727 AGCTGCTGTCGGAACCCAGCTCTTACCCAGAGAGGTGCTGGCGGCGGGGCGGCGGAAGGTTGCCT AGCTGCTGTCGGAACCCAGCTCTTACCCAGAGTGGTGCTGGCGGCGGGGCGGCGGAAGGTTGCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:197902677..197902841 26863196 MeRIP-seq:(Medium) rs1183267366 Functional Loss SNV dbSNP153 33..33 33 - - - 76261 RMVar_ID_76261 Human_SNP_ID_45266004 m1A Human chr1 + 198157076 198157076 198157076 GAGGATGGGCCGCCGCTAGGCTCGCACTCCGGACGCGCCTCGCAGTGCGCAGGGTGGGTGCCCCG GAGGATGGGCCGCCGCTAGGCTCGCACTCCGGCCGCGCCTCGCAGTGCGCAGGGTGGGTGCCCCG A C NEK7 Ensembl:ENSG00000151414 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:198157026..198157182 26863196 MeRIP-seq:(Medium) rs548492730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4015690,Human_RBP_ID_5311914,Human_RBP_ID_17734960,Human_RBP_ID_18415124,Human_RBP_ID_22871017 Human_Splice_Rec_170095 76262 RMVar_ID_76262 Human_SNP_ID_45266011 m1A Human chr1 - 198157098 198157094 198157098 GCCCCGGCGGACGCTGCAGGCGCGGGGCACCCACCCTGCGCACTGCGAGGCGCGTCCGGAGTGCG GCCCCGGCGGACGCTGCAGGCGCGGGGCACCC____TGCGCACTGCGAGGCGCGTCCGGAGTGCG AGGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:198157047..198157178 26863196 MeRIP-seq:(Medium) rs1276495503 Functional Loss DEL dbSNP153 33..36 33 - - - 76263 RMVar_ID_76263 Human_SNP_ID_45266015 m1A Human chr1 - 198157098 198157098 198157098 GCCCCGGCGGACGCTGCAGGCGCGGGGCACCCACCCTGCGCACTGCGAGGCGCGTCCGGAGTGCG GCCCCGGCGGACGCTGCAGGCGCGGGGCACCCCCCCTGCGCACTGCGAGGCGCGTCCGGAGTGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:198157047..198157178 26863196 MeRIP-seq:(Medium) rs1012716044 Functional Loss SNV dbSNP153 33..33 33 - - - 76264 RMVar_ID_76264 Human_SNP_ID_45266059 m1A Human chr1 + 198157200 198157200 198157200 CAGCCTCAGCCCCCGGCCCAGCGCGCTTTCCGACGGCGGCGCCGCGCCGAGCCACCCGCCCGCCC CAGCCTCAGCCCCCGGCCCAGCGCGCTTTCCGGCGGCGGCGCCGCGCCGAGCCACCCGCCCGCCC A G NEK7 Ensembl:ENSG00000151414 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:198157062..198206909 26863410 MeRIP-seq:(Medium) rs1041476442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337110,Human_RBP_ID_4015697 Human_Splice_Rec_170089,Human_Splice_Rec_170113,Human_Splice_Rec_170131 76265 RMVar_ID_76265 Human_SNP_ID_45268841 m1A Human chr1 + 198168773 198168773 198168773 ACCAAAGAAAGATAAATTTGGGAGTTGTTGGTAGGTAGCTGAAAGTGAATGAAATGATTACAATT ACCAAAGAAAGATAAATTTGGGAGTTGTTGGTGGGTAGCTGAAAGTGAATGAAATGATTACAATT A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:198168769..198168907 26863196 MeRIP-seq:(Medium) rs1040953215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9476650 76266 RMVar_ID_76266 Human_SNP_ID_45275175 m1A Human chr1 - 198197816 198197816 198197816 CAAAAAGATGCACAAGCACCACGAGCATGGCAAGCATTCCTCCTCCTCTTCCATCAGTGACTCTG CAAAAAGATGCACAAGCACCACGAGCATGGCAGGCATTCCTCCTCCTCTTCCATCAGTGACTCTG T C PRR13P1 Ensembl:ENSG00000232824 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:198197814..198198192 26863196 MeRIP-seq:(Medium) rs1003968296 Functional Loss SNV dbSNP153 33..33 33 - - - 76267 RMVar_ID_76267 Human_SNP_ID_45283827 m1A Human chr1 + 198232576 198232576 198232576 TTTTTGCAGAGTTCTAAAGTTCCTGTTGCTTCAGACAATGGATGAGCAATCACAAGGAATGCAAG TTTTTGCAGAGTTCTAAAGTTCCTGTTGCTTCGGACAATGGATGAGCAATCACAAGGAATGCAAG A G NEK7 Ensembl:ENSG00000151414 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:198232571..198245223 32194978 MeRIP-seq:(Medium) rs1271336030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21635,Human_RBP_ID_337115,Human_RBP_ID_1418249 Human_Splice_Rec_170092,Human_Splice_Rec_170093,Human_Splice_Rec_170096,Human_Splice_Rec_170097,Human_Splice_Rec_170114,Human_Splice_Rec_170115,Human_Splice_Rec_170132,Human_Splice_Rec_170133,Human_Splice_Rec_170138,Human_Splice_Rec_170139,Human_Splice_Rec_170144,Human_Splice_Rec_170145,Human_Splice_Rec_170148,Human_Splice_Rec_170149 RMVar_hsa_circ_138667,RMVar_hsa_circ_90339,RMVar_hsa_circ_314608,RMVar_hsa_circ_94783,RMVar_hsa_circ_138668,RMVar_hsa_circ_138669,RMVar_hsa_circ_138671,RMVar_hsa_circ_117693,RMVar_hsa_circ_276992,RMVar_hsa_circ_292860,RMVar_hsa_circ_303608,RMVar_hsa_circ_292471,RMVar_hsa_circ_272919,RMVar_hsa_circ_138673,RMVar_hsa_circ_138674,RMVar_hsa_circ_138672,RMVar_hsa_circ_138670 76268 RMVar_ID_76268 Human_SNP_ID_45295115 m1A Human chr1 + 198279060 198279060 198279060 TTCAGCTCAAAAACCACAGCTGCACATTCTTTAGGTAAGAGACACAATATAATTTCATTCAGTTA TTCAGCTCAAAAACCACAGCTGCACATTCTTTTGGTAAGAGACACAATATAATTTCATTCAGTTA A T NEK7 Ensembl:ENSG00000151414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:198279037..198293021 32194978 MeRIP-seq:(Medium) rs772989091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17734991,Human_RBP_ID_19042110,Human_RBP_ID_26799299,Human_RBP_ID_27584182 Human_Splice_Rec_170107,Human_Splice_Rec_170125,Human_Splice_Rec_170155 RMVar_hsa_circ_138669,RMVar_hsa_circ_138671,RMVar_hsa_circ_292860,RMVar_hsa_circ_303608,RMVar_hsa_circ_272919,RMVar_hsa_circ_351069,RMVar_hsa_circ_138670,RMVar_hsa_circ_345173,RMVar_hsa_circ_138678,RMVar_hsa_circ_281371,RMVar_hsa_circ_28586,RMVar_hsa_circ_307169,RMVar_hsa_circ_15578,RMVar_hsa_circ_138680,RMVar_hsa_circ_114107,RMVar_hsa_circ_138679,RMVar_hsa_circ_17821,RMVar_hsa_circ_138682,RMVar_hsa_circ_138681,RMVar_hsa_circ_278586,RMVar_hsa_circ_367458,RMVar_hsa_circ_333223 76269 RMVar_ID_76269 Human_SNP_ID_45296438 m1A Human chr1 - 198284960 198284960 198284960 TGTAACTTACTGTACCCACAACACTGAGGAACAGAGGAGAAAACGTGCTTTAAAATGCTCAGAAA TGTAACTTACTGTACCCACAACACTGAGGAACGGAGGAGAAAACGTGCTTTAAAATGCTCAGAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:198284945..198285028 26863196 MeRIP-seq:(Medium) rs1259912829 Functional Loss SNV dbSNP153 33..33 33 - - - 76270 RMVar_ID_76270 Human_SNP_ID_45799023 m1A Human chr1 + 200409476 200409476 200409476 CGGCCGGGGCTGCGGAGGTAGAGGAGGATAACACGCATTGCGGGGGAGGGGCGGCCGACCCCGCC CGGCCGGGGCTGCGGAGGTAGAGGAGGATAACGCGCATTGCGGGGGAGGGGCGGCCGACCCCGCC A G AC104461.1 Ensembl:ENSG00000230623 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:200409384..200409484 26863410 MeRIP-seq:(Medium) rs1214542996 Functional Loss SNV dbSNP153 33..33 33 - - - 76271 RMVar_ID_76271 Human_SNP_ID_45799127 m1A Human chr1 + 200409642 200409621 200409642 GCCGCCGCCGCCGCCACTACCACCGCCGCCGGAGCCGCTACCACCGCTACTGCCGGTACCTCCGC GCCGCCGCCGCC_____________________GCCGCTACCACCGCTACTGCCGGTACCTCCGC CGCCACTACCACCGCCGCCGGA C AC104461.1 Ensembl:ENSG00000230623 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:200409594..200409725;chr1:200409638..200409784 26863196 MeRIP-seq:(Medium) rs1177962977 Functional Loss DEL dbSNP153 13..33 33 - - - 76272 RMVar_ID_76272 Human_SNP_ID_45799163 m1A Human chr1 - 200409699 200409699 200409699 TTCTTCAGCCAGGCCTCCTCCGGGGTATGAAAATCGGCAGTGGGTTCCTGAGTGGCGGCGGAGGT TTCTTCAGCCAGGCCTCCTCCGGGGTATGAAAGTCGGCAGTGGGTTCCTGAGTGGCGGCGGAGGT T C ZNF281 Ensembl:ENSG00000162702 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:200409625..200409804 26863196 MeRIP-seq:(Medium) rs1373064525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19039918,Human_RBP_ID_24748934 Human_Splice_Rec_170720,Human_Splice_Rec_170722,Human_Splice_Rec_170724 76273 RMVar_ID_76273 Human_SNP_ID_45799268 m1A Human chr1 - 200409982 200409982 200409982 CCATTGTGGAGAGGACGGCGTTATTTTTATTAACTGGAGGCGACGGCGGCTGCGGCGGCGGCGGG CCATTGTGGAGAGGACGGCGTTATTTTTATTACCTGGAGGCGACGGCGGCTGCGGCGGCGGCGGG T G ZNF281 Ensembl:ENSG00000162702 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200409131..200410050 26863196 MeRIP-seq:(Medium) rs918337251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745435,Human_RBP_ID_973784,Human_RBP_ID_4016034,Human_RBP_ID_5433375,Human_RBP_ID_5485147,Human_RBP_ID_8045397,Human_RBP_ID_17735201,Human_RBP_ID_22024080,Human_RBP_ID_27584338 Human_Splice_Rec_170719,Human_Splice_Rec_170721,Human_Splice_Rec_170723 76274 RMVar_ID_76274 Human_SNP_ID_45799269 m1A Human chr1 + 200409985 200409985 200409985 GCCGCCGCCGCAGCCGCCGTCGCCTCCAGTTAATAAAAATAACGCCGTCCTCTCCACAATGGAAT GCCGCCGCCGCAGCCGCCGTCGCCTCCAGTTATTAAAAATAACGCCGTCCTCTCCACAATGGAAT A T AC104461.1 Ensembl:ENSG00000230623 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:200409917..200410014 26863196 MeRIP-seq:(Medium) rs1481320184 Functional Loss SNV dbSNP153 33..33 33 - - - 76275 RMVar_ID_76275 Human_SNP_ID_45814803 m1A Human chr1 + 200479795 200479795 200479795 TCCTCCCAGCCTAGCCTCTCCAGCCCGTGACCAGCCTCCCAGCCCAGCCTCTCCAGCCCAGGCCA TCCTCCCAGCCTAGCCTCTCCAGCCCGTGACCGGCCTCCCAGCCCAGCCTCTCCAGCCCAGGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200479566..200479868 26863196 MeRIP-seq:(Medium) rs1352145001 Functional Loss SNV dbSNP153 33..33 33 - - - 76276 RMVar_ID_76276 Human_SNP_ID_45816830 m1A Human chr1 + 200487906 200487899 200487906 GGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGA GGGGGGGGGGGGGGGGGGGGGGGGGG_______GAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGA GAGGGAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:200487847..200487918 26863196 MeRIP-seq:(Medium) rs1558021251 Functional Loss DEL dbSNP153 27..33 33 - - - 76277 RMVar_ID_76277 Human_SNP_ID_45816845 m1A Human chr1 + 200487906 200487906 200487906 GGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGAGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGA GGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGGGAGAGAGAGAGAGGGAGAGAGAGAGAGAGAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:200487847..200487918 26863196 MeRIP-seq:(Medium) rs201289418 Functional Loss SNV dbSNP153 33..33 33 - - - 76278 RMVar_ID_76278 Human_SNP_ID_45849733 m1A Human chr1 + 200620581 200620580 200620581 GCTGAGGAACTGAATGGGGGACTGGAGCTAAGACCACCCGCCCGCAGAGCAGTGGTCGCCTGTAG GCTGAGGAACTGAATGGGGGACTGGAGCTAAG_CCACCCGCCCGCAGAGCAGTGGTCGCCTGTAG GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:200620531..200620678 26863196 MeRIP-seq:(Medium) rs768053351 Functional Loss DEL dbSNP153 33..33 33 - - - 76279 RMVar_ID_76279 Human_SNP_ID_45857826 m1A Human chr1 + 200653695 200653695 200653695 TCTCTGACTTCATCTCCAAGCACTCTCCCCTCACTGCTCGTGACTCTGCCACACCAGCCTTCCTT TCTCTGACTTCATCTCCAAGCACTCTCCCCTCGCTGCTCGTGACTCTGCCACACCAGCCTTCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200653599..200653850 26863196 MeRIP-seq:(Medium) rs1247069167 Functional Loss SNV dbSNP153 33..33 33 - - - 76280 RMVar_ID_76280 Human_SNP_ID_45858279 m1A Human chr1 - 200655415 200655415 200655415 GTGGTTTAAGAGGTTACCCTGCTGCGTGATACAGGAGAAATGAAAGAATCTAAGAGCAGCCAGCA GTGGTTTAAGAGGTTACCCTGCTGCGTGATACGGGAGAAATGAAAGAATCTAAGAGCAGCCAGCA T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200655364..200655592 26863196 MeRIP-seq:(Medium) rs914678591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10721337 RMVar_hsa_circ_138724,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725,RMVar_hsa_circ_364449 76281 RMVar_ID_76281 Human_SNP_ID_45858473 m1A Human chr1 - 200656288 200656288 200656288 CTTTCTGTAAAGGACCAGATGGTAAATATCTTAGGCTTTGGGGGCCAATGTAGATGGTATGAAGA CTTTCTGTAAAGGACCAGATGGTAAATATCTTGGGCTTTGGGGGCCAATGTAGATGGTATGAAGA T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200656237..200656324 26863196 MeRIP-seq:(Medium) rs545935643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1151271 RMVar_hsa_circ_138724,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725,RMVar_hsa_circ_364449 76282 RMVar_ID_76282 Human_SNP_ID_45879002 m1A Human chr1 - 200739006 200739006 200739006 CTCAGTTCCTGTCTTATCAGTAATGTCCTTGTAATTTTTTCCTGCCCCCCTTTCTGCAGCTCGCT CTCAGTTCCTGTCTTATCAGTAATGTCCTTGTGATTTTTTCCTGCCCCCCTTTCTGCAGCTCGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:200738926..200739436;chr1:200738926..200739433 26863196 MeRIP-seq:(Medium) rs1044561187 Functional Loss SNV dbSNP153 33..33 33 - - - 76283 RMVar_ID_76283 Human_SNP_ID_45915009 m1A Human chr1 + 200891089 200891088 200891089 GTGGGCCGGGGCCAGGGCCGGGGAGAGGGGCCATCCCCGCGCGACCCGCAGCGCCGCACAGCGAG GTGGGCCGGGGCCAGGGCCGGGGAGAGGGGCC_TCCCCGCGCGACCCGCAGCGCCGCACAGCGAG CA C INAVA Ensembl:ENSG00000163362 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:200891040..200891199 26863196 MeRIP-seq:(Medium) rs1424955137 Functional Loss DEL dbSNP153 33..33 33 - - - 76284 RMVar_ID_76284 Human_SNP_ID_45915030 m1A Human chr1 - 200891150 200891149 200891151 ATGAAAGGAGCCTGCGGAAGGGCGCTCCCCCGACCCTGTCCTCCCCGCAGGCGCCCTCCCCCTCG ATGAAAGGAGCCTGCGGAAGGGCGCTCCCCC__CCCTGTCCTCCCCGCAGGCGCCCTCCCCCTCG GTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:200891043..200891206 26863196 MeRIP-seq:(Medium) rs1265843941 Functional Loss DEL dbSNP153 32..33 33 - - - 76285 RMVar_ID_76285 Human_SNP_ID_45915204 m1A Human chr1 + 200891608 200891608 200891608 GGGGAGGGCAGGCCGCAGGGAGGCTCGGGGGGAGGGAAGATGGCCTGGACAAACAGGTCCTGAAG GGGGAGGGCAGGCCGCAGGGAGGCTCGGGGGGGGGGAAGATGGCCTGGACAAACAGGTCCTGAAG A G INAVA Ensembl:ENSG00000163362 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200891580..200891750 26863196 MeRIP-seq:(Medium) rs1164298278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_171027 76286 RMVar_ID_76286 Human_SNP_ID_45940427 m1A Human chr1 - 200992371 200992371 200992371 TCTGCCCATCCCAGGTGGCCCTGATGAAGCAGATGCGTGAGGAGCAACAGCGGCGGCGGCTAGTG TCTGCCCATCCCAGGTGGCCCTGATGAAGCAGGTGCGTGAGGAGCAACAGCGGCGGCGGCTAGTG T C KIF21B Ensembl:ENSG00000116852 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:200992261..200992434 26863196 MeRIP-seq:(Medium) rs1343815266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27801345 Human_Splice_Rec_171182,Human_Splice_Rec_171183,Human_Splice_Rec_171248,Human_Splice_Rec_171249,Human_Splice_Rec_171314,Human_Splice_Rec_171315,Human_Splice_Rec_171382,Human_Splice_Rec_171383 RMVar_hsa_circ_26208,RMVar_hsa_circ_21819,RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_49544,RMVar_hsa_circ_41431,RMVar_hsa_circ_138770 76287 RMVar_ID_76287 Human_SNP_ID_45941302 m1A Human chr1 - 200996135 200996135 200996135 CCTGGAGTGCCTGTGACATCTTCTTAGAATCCACTCACCATCGTAAAAATAATCATTGCTGTCAA CCTGGAGTGCCTGTGACATCTTCTTAGAATCCGCTCACCATCGTAAAAATAATCATTGCTGTCAA T C KIF21B Ensembl:ENSG00000116852 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200996132..200996323 26863196 MeRIP-seq:(Medium) rs907667789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26208,RMVar_hsa_circ_21819,RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_49544,RMVar_hsa_circ_41431,RMVar_hsa_circ_138770 76288 RMVar_ID_76288 Human_SNP_ID_45941303 m1A Human chr1 - 200996135 200996135 200996135 CCTGGAGTGCCTGTGACATCTTCTTAGAATCCACTCACCATCGTAAAAATAATCATTGCTGTCAA CCTGGAGTGCCTGTGACATCTTCTTAGAATCCCCTCACCATCGTAAAAATAATCATTGCTGTCAA T G KIF21B Ensembl:ENSG00000116852 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200996132..200996323 26863196 MeRIP-seq:(Medium) rs907667789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26208,RMVar_hsa_circ_21819,RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_49544,RMVar_hsa_circ_41431,RMVar_hsa_circ_138770 76289 RMVar_ID_76289 Human_SNP_ID_45942224 m1A Human chr1 - 200999432 200999432 200999432 GGAGGAAGAGCGAGACGAGAGTGGCTGTGAGGAGGAGGAAGGGCGCGAGGATGAAGATGAGGACT GGAGGAAGAGCGAGACGAGAGTGGCTGTGAGGGGGAGGAAGGGCGCGAGGATGAAGATGAGGACT T C KIF21B Ensembl:ENSG00000116852 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:200999381..200999495 26863196 MeRIP-seq:(Medium) rs772782924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_171176,Human_Splice_Rec_171177,Human_Splice_Rec_171242,Human_Splice_Rec_171243,Human_Splice_Rec_171308,Human_Splice_Rec_171309,Human_Splice_Rec_171376,Human_Splice_Rec_171377 RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_67853 76290 RMVar_ID_76290 Human_SNP_ID_45942397 m1A Human chr1 - 200999934 200999934 200999934 AGCCCCGAGAAGGAAGCCTTCAAAAAGAGGGCAAAACTCCAACAGGAGAACAGCGAGGAGACGGA AGCCCCGAGAAGGAAGCCTTCAAAAAGAGGGCGAAACTCCAACAGGAGAACAGCGAGGAGACGGA T C KIF21B Ensembl:ENSG00000116852 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:200999830..200999956 26863196 MeRIP-seq:(Medium) rs777511015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26312470 Human_Splice_Rec_171174,Human_Splice_Rec_171175,Human_Splice_Rec_171240,Human_Splice_Rec_171241,Human_Splice_Rec_171306,Human_Splice_Rec_171307,Human_Splice_Rec_171374,Human_Splice_Rec_171375 RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_67853 76291 RMVar_ID_76291 Human_SNP_ID_45942517 m1A Human chr1 - 201000343 201000343 201000343 GTCCCCGCCCCTGAGAGCCCTCAGACCGCCCCAGTGGACCCTGCCCGTCCCCAAGGAGGACTGCT GTCCCCGCCCCTGAGAGCCCTCAGACCGCCCCGGTGGACCCTGCCCGTCCCCAAGGAGGACTGCT T C KIF21B Ensembl:ENSG00000116852 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201000342..201000465 26863196 MeRIP-seq:(Medium) rs746965843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_67853 76292 RMVar_ID_76292 Human_SNP_ID_45948464 m1A Human chr1 - 201023439 201023435 201023439 CGCCTCCCGCAGCCGCAGCCGCTGCCTCGGGCATTGGCCCCCAGACCCCCGCCTCTGATCCACGC CGCCTCCCGCAGCCGCAGCCGCTGCCTCGGGC____GCCCCCAGACCCCCGCCTCTGATCCACGC CCAAT C KIF21B Ensembl:ENSG00000116852 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201023389..201023667 26863196 MeRIP-seq:(Medium) rs1019798260 Functional Loss DEL dbSNP153 33..36 33 - - - Human_Splice_Rec_171153,Human_Splice_Rec_171219,Human_Splice_Rec_171285,Human_Splice_Rec_171353 76293 RMVar_ID_76293 Human_SNP_ID_45948476 m1A Human chr1 + 201023467 201023467 201023467 CCAATGCCCGAGGCAGCGGCTGCGGCTGCGGGAGGCGGGGGCGCGGGCGCGGCTGGCGGAGGCTG CCAATGCCCGAGGCAGCGGCTGCGGCTGCGGGGGGCGGGGGCGCGGGCGCGGCTGGCGGAGGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201023422..201023639 26863196 MeRIP-seq:(Medium) rs986768265 Functional Loss SNV dbSNP153 33..33 33 - - - 76294 RMVar_ID_76294 Human_SNP_ID_45978790 m1A Human chr1 - 201135259 201135259 201135259 TGGGTCTTCAGGAACTCAGTGTCTGGGAGGAAAGCATGGCCCAGCATTCAGCATGTGTTCCTTTC TGGGTCTTCAGGAACTCAGTGTCTGGGAGGAACGCATGGCCCAGCATTCAGCATGTGTTCCTTTC T G TMEM9 Ensembl:ENSG00000116857 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201135208..201135297 26863196 MeRIP-seq:(Medium) rs1313278218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337557,Human_RBP_ID_973809,Human_RBP_ID_1733133,Human_RBP_ID_3292350,Human_RBP_ID_8171009,Human_RBP_ID_10723007,Human_RBP_ID_17676116,Human_RBP_ID_17763056,Human_RBP_ID_23145989 RMVar_hsa_circ_77213,RMVar_hsa_circ_113941,RMVar_hsa_circ_119917,RMVar_hsa_circ_97177,RMVar_hsa_circ_138784,RMVar_hsa_circ_138786,RMVar_hsa_circ_76775,RMVar_hsa_circ_138787,RMVar_hsa_circ_138785,RMVar_hsa_circ_138783 76295 RMVar_ID_76295 Human_SNP_ID_45978812 m1A Human chr1 - 201135350 201135350 201135350 AGGAGTGGATGCGATCTGTCTCTCCTGGCTCCACTCTTGCCGCCTTCCAGCTCTGAGTCTTGGGA AGGAGTGGATGCGATCTGTCTCTCCTGGCTCCTCTCTTGCCGCCTTCCAGCTCTGAGTCTTGGGA T A TMEM9 Ensembl:ENSG00000116857 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:201135301..201135515 32194978 MeRIP-seq:(Medium) rs1352520323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337558,Human_RBP_ID_5108867,Human_RBP_ID_5136451,Human_RBP_ID_8171010,Human_RBP_ID_8294849,Human_RBP_ID_9320304,Human_RBP_ID_10723010,Human_RBP_ID_17647204,Human_RBP_ID_17735342,Human_RBP_ID_18187347,Human_RBP_ID_18222057,Human_RBP_ID_22369309,Human_RBP_ID_26373845,Human_RBP_ID_26799309,Human_RBP_ID_27392476,Human_RBP_ID_27554786 Human_miRNA_ID_2345185 RMVar_hsa_circ_77213,RMVar_hsa_circ_113941,RMVar_hsa_circ_119917,RMVar_hsa_circ_97177,RMVar_hsa_circ_138784,RMVar_hsa_circ_138786,RMVar_hsa_circ_76775,RMVar_hsa_circ_138787,RMVar_hsa_circ_138785,RMVar_hsa_circ_138783 76296 RMVar_ID_76296 Human_SNP_ID_45981021 m1A Human chr1 - 201143868 201143868 201143868 GCCTTCCTGATGCTGGTGGACCCTCTGATCCGAAAGCCGGATGCATATACTGAGCAACTGCACAA GCCTTCCTGATGCTGGTGGACCCTCTGATCCGCAAGCCGGATGCATATACTGAGCAACTGCACAA T G TMEM9 Ensembl:ENSG00000116857 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201143765..201143981 26863196 MeRIP-seq:(Medium) rs1386882298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337575,Human_RBP_ID_1418566,Human_RBP_ID_3292353,Human_RBP_ID_8961061,Human_RBP_ID_10723077,Human_RBP_ID_18559728,Human_RBP_ID_22427747,Human_RBP_ID_22749710,Human_RBP_ID_23355414,Human_RBP_ID_26373863,Human_RBP_ID_26799311 Human_Splice_Rec_171616,Human_Splice_Rec_171617,Human_Splice_Rec_171626,Human_Splice_Rec_171627,Human_Splice_Rec_171636,Human_Splice_Rec_171637,Human_Splice_Rec_171639,Human_Splice_Rec_171648,Human_Splice_Rec_171649,Human_Splice_Rec_171658,Human_Splice_Rec_171659,Human_Splice_Rec_171668,Human_Splice_Rec_171669,Human_Splice_Rec_171676,Human_Splice_Rec_171677,Human_Splice_Rec_171684,Human_Splice_Rec_171685,Human_Splice_Rec_171694,Human_Splice_Rec_171695,Human_Splice_Rec_171704,Human_Splice_Rec_171705 RMVar_hsa_circ_77213,RMVar_hsa_circ_113941,RMVar_hsa_circ_119917,RMVar_hsa_circ_97177,RMVar_hsa_circ_28143,RMVar_hsa_circ_138784,RMVar_hsa_circ_138786,RMVar_hsa_circ_76775,RMVar_hsa_circ_138787,RMVar_hsa_circ_138785,RMVar_hsa_circ_123112,RMVar_hsa_circ_374918,RMVar_hsa_circ_138783,RMVar_hsa_circ_284528,RMVar_hsa_circ_80141,RMVar_hsa_circ_138788,RMVar_hsa_circ_138790,RMVar_hsa_circ_138791,RMVar_hsa_circ_138789 76297 RMVar_ID_76297 Human_SNP_ID_45983621 m1A Human chr1 - 201154136 201154136 201154136 CCCCTCTGCCGGGCTCACCAGGTGGCTGGCGGAGAGCCGGAGAGTTGGGCGGGAGGGAAGCAGGG CCCCTCTGCCGGGCTCACCAGGTGGCTGGCGGGGAGCCGGAGAGTTGGGCGGGAGGGAAGCAGGG T C TMEM9 Ensembl:ENSG00000116857 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201154134..201154450 26863196 MeRIP-seq:(Medium) rs1421819997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8961063 RMVar_hsa_circ_113941,RMVar_hsa_circ_97177,RMVar_hsa_circ_138786,RMVar_hsa_circ_138787,RMVar_hsa_circ_123112,RMVar_hsa_circ_80141,RMVar_hsa_circ_138788,RMVar_hsa_circ_138789 76298 RMVar_ID_76298 Human_SNP_ID_45983652 m1A Human chr1 - 201154235 201154235 201154235 GAGGCGGAGATGGCGGAGGGCGGTGGGACGTGATGCGCGGGTCAGAGCCGGGCCTTGAGAAGGAA GAGGCGGAGATGGCGGAGGGCGGTGGGACGTGGTGCGCGGGTCAGAGCCGGGCCTTGAGAAGGAA T C TMEM9 Ensembl:ENSG00000116857 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:201154184..201154353 26863196 MeRIP-seq:(Medium) rs1456903688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804271,Human_RBP_ID_3330497,Human_RBP_ID_5311922,Human_RBP_ID_5334034,Human_RBP_ID_8227852,Human_RBP_ID_9410706,Human_RBP_ID_18928828,Human_RBP_ID_19042119,Human_RBP_ID_22634813,Human_RBP_ID_23255402,Human_RBP_ID_26774661 Human_Splice_Rec_171661 RMVar_hsa_circ_113941,RMVar_hsa_circ_97177,RMVar_hsa_circ_138786,RMVar_hsa_circ_138787,RMVar_hsa_circ_123112,RMVar_hsa_circ_80141,RMVar_hsa_circ_138788,RMVar_hsa_circ_138789 76299 RMVar_ID_76299 Human_SNP_ID_45983698 m1A Human chr1 - 201154374 201154374 201154374 CGGGGCTATTGGGGGTCCCAGTCCGGCTTAAGACCTCTGGGCGTGGTGGGCACCGGCCTTCGCCG CGGGGCTATTGGGGGTCCCAGTCCGGCTTAAGGCCTCTGGGCGTGGTGGGCACCGGCCTTCGCCG T C TMEM9 Ensembl:ENSG00000116857 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:201154341..201154472 26863410 MeRIP-seq:(Medium) rs1358598079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804272,Human_RBP_ID_3328740,Human_RBP_ID_4016415,Human_RBP_ID_5332195,Human_RBP_ID_8167281,Human_RBP_ID_8227853,Human_RBP_ID_9410707,Human_RBP_ID_18415127,Human_RBP_ID_19035811,Human_RBP_ID_22635798 Human_Splice_Rec_171687 RMVar_hsa_circ_113941,RMVar_hsa_circ_97177,RMVar_hsa_circ_138786,RMVar_hsa_circ_138787,RMVar_hsa_circ_123112,RMVar_hsa_circ_80141,RMVar_hsa_circ_138788,RMVar_hsa_circ_138789 76300 RMVar_ID_76300 Human_SNP_ID_45997026 m1A Human chr1 - 201206741 201206741 201206741 ATCTGCTTTCCTCTTGGCCAGGACCCTACAGGATCAGACTGGCATCCCTGCAGGTCGCTCTTTCC ATCTGCTTTCCTCTTGGCCAGGACCCTACAGGGTCAGACTGGCATCCCTGCAGGTCGCTCTTTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201206702..201206816 26863196 MeRIP-seq:(Medium) rs757407745 Functional Loss SNV dbSNP153 33..33 33 - - - 76301 RMVar_ID_76301 Human_SNP_ID_45997926 m1A Human chr1 - 201209103 201209103 201209103 AATCCCATTCCTATGACCTGACTCATCCAGTGACCCCATCTCCCCAGGACCCCTTAAACCAGCCC AATCCCATTCCTATGACCTGACTCATCCAGTGGCCCCATCTCCCCAGGACCCCTTAAACCAGCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201208652..201209258 26863196 MeRIP-seq:(Medium) rs1004093559 Functional Loss SNV dbSNP153 33..33 33 - - - 76302 RMVar_ID_76302 Human_SNP_ID_45998367 m1A Human chr1 + 201209945 201209945 201209945 TATAGGAAGAATTTGGGGGCTCCTGAGGGAATAGGTTCAGGGAGTAAGGCAGGTTTTAGGGATGG TATAGGAAGAATTTGGGGGCTCCTGAGGGAATGGGTTCAGGGAGTAAGGCAGGTTTTAGGGATGG A G IGFN1 Ensembl:ENSG00000163395 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201209842..201209973 26863196 MeRIP-seq:(Medium) rs374391246 Functional Loss SNV dbSNP153 33..33 33 - - - 76303 RMVar_ID_76303 Human_SNP_ID_46067669 m1A Human chr1 + 201465625 201465623 201465626 CGCAGTGGGGGGAAGATGCGTAGAGGTGGGGGAAGAAGTGTGCAAAGAAAGGGCCTGGATGGGTG CGCAGTGGGGGGAAGATGCGTAGAGGTGGGG___GAAGTGTGCAAAGAAAGGGCCTGGATGGGTG GGAA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:201465576..201466176 32194978 MeRIP-seq:(Medium) rs966802658 Functional Loss DEL dbSNP153 32..34 33 - - - 76304 RMVar_ID_76304 Human_SNP_ID_46067670 m1A Human chr1 + 201465625 201465625 201465625 CGCAGTGGGGGGAAGATGCGTAGAGGTGGGGGAAGAAGTGTGCAAAGAAAGGGCCTGGATGGGTG CGCAGTGGGGGGAAGATGCGTAGAGGTGGGGGCAGAAGTGTGCAAAGAAAGGGCCTGGATGGGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:201465576..201466176 32194978 MeRIP-seq:(Medium) rs1376181591 Functional Loss SNV dbSNP153 33..33 33 - - - 76305 RMVar_ID_76305 Human_SNP_ID_46067799 m1A Human chr1 + 201466096 201466096 201466096 TCCTCCCAGGGCTCGTCCATTCCTTCAGCTCCAGCGCCTCCTCCACACGTCCATGCCTTCCACCT TCCTCCCAGGGCTCGTCCATTCCTTCAGCTCCCGCGCCTCCTCCACACGTCCATGCCTTCCACCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201465880..201466357 26863196 MeRIP-seq:(Medium) rs1024879523 Functional Loss SNV dbSNP153 33..33 33 - - - 76306 RMVar_ID_76306 Human_SNP_ID_46068779 m1A Human chr1 - 201468839 201468839 201468839 GGGGCGCCAGAATCCTGCGCTGCGGGGCCGAGAGGGGCGCCGCGCCCGCCGCAGCCTGGAGCTTT GGGGCGCCAGAATCCTGCGCTGCGGGGCCGAGGGGGGCGCCGCGCCCGCCGCAGCCTGGAGCTTT T C PHLDA3 Ensembl:ENSG00000174307 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:201468738..201468938 26863410 MeRIP-seq:(Medium) rs1051503045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803778,Human_RBP_ID_4076282,Human_RBP_ID_9352539 RMVar_hsa_circ_83572,RMVar_hsa_circ_138803 76307 RMVar_ID_76307 Human_SNP_ID_46068849 m1A Human chr1 - 201469022 201469022 201469022 CGGGTCGGGCTGGGCCAGCTGGGGTAGAGCGGAGGAGCGGGTGCCGGCTGAAGCGGGGCGGTGGG CGGGTCGGGCTGGGCCAGCTGGGGTAGAGCGGTGGAGCGGGTGCCGGCTGAAGCGGGGCGGTGGG T A PHLDA3 Ensembl:ENSG00000174307 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:201468326..201469250;chr1:201468376..201469275;chr1:201468340..201469250 26863196 MeRIP-seq:(Medium) rs1051484545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222922,Human_RBP_ID_803779,Human_RBP_ID_4016499,Human_RBP_ID_9352541,Human_RBP_ID_9412662,Human_RBP_ID_17647836,Human_RBP_ID_22026522,Human_RBP_ID_22429944 RMVar_hsa_circ_83572,RMVar_hsa_circ_138803 76308 RMVar_ID_76308 Human_SNP_ID_46068850 m1A Human chr1 - 201469022 201469022 201469022 CGGGTCGGGCTGGGCCAGCTGGGGTAGAGCGGAGGAGCGGGTGCCGGCTGAAGCGGGGCGGTGGG CGGGTCGGGCTGGGCCAGCTGGGGTAGAGCGGCGGAGCGGGTGCCGGCTGAAGCGGGGCGGTGGG T G PHLDA3 Ensembl:ENSG00000174307 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:201468326..201469250;chr1:201468376..201469275;chr1:201468340..201469250 26863196 MeRIP-seq:(Medium) rs1051484545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222922,Human_RBP_ID_803779,Human_RBP_ID_4016499,Human_RBP_ID_9352541,Human_RBP_ID_9412662,Human_RBP_ID_17647836,Human_RBP_ID_22026522,Human_RBP_ID_22429944 RMVar_hsa_circ_83572,RMVar_hsa_circ_138803 76309 RMVar_ID_76309 Human_SNP_ID_46068872 m1A Human chr1 - 201469070 201469070 201469070 GGCGGTGGGGCTCACGGCCTAGGGAGGCGCGGAGGCATCTGGCAGAGGCGGGTCGGGCTGGGCCA GGCGGTGGGGCTCACGGCCTAGGGAGGCGCGGGGGCATCTGGCAGAGGCGGGTCGGGCTGGGCCA T C PHLDA3 Ensembl:ENSG00000174307 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:201468876..201469231 26863196 MeRIP-seq:(Medium) rs1055951139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973820,Human_RBP_ID_4073223,Human_RBP_ID_9352541,Human_RBP_ID_9412662,Human_RBP_ID_22429944 RMVar_hsa_circ_83572,RMVar_hsa_circ_138803 76310 RMVar_ID_76310 Human_SNP_ID_46073753 m1A Human chr1 - 201488986 201488986 201488986 TAAGTCACCTCACCCCATGCCCTTCTCCATGCAGAGCCCCTGGCCACAGGCCCACCACCAACCCC TAAGTCACCTCACCCCATGCCCTTCTCCATGCTGAGCCCCTGGCCACAGGCCCACCACCAACCCC T A CSRP1 Ensembl:ENSG00000159176 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:201488857..201489036;chr1:201488904..201489029;chr1:201488798..201489036 26863196 MeRIP-seq:(Medium) rs111791241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2569,RMVar_hsa_circ_86124,RMVar_hsa_circ_127254,RMVar_hsa_circ_138806,RMVar_hsa_circ_138807,RMVar_hsa_circ_138809,RMVar_hsa_circ_295982 76311 RMVar_ID_76311 Human_SNP_ID_46073754 m1A Human chr1 - 201488986 201488986 201488986 TAAGTCACCTCACCCCATGCCCTTCTCCATGCAGAGCCCCTGGCCACAGGCCCACCACCAACCCC TAAGTCACCTCACCCCATGCCCTTCTCCATGCGGAGCCCCTGGCCACAGGCCCACCACCAACCCC T C CSRP1 Ensembl:ENSG00000159176 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:201488857..201489036;chr1:201488904..201489029;chr1:201488798..201489036 26863196 MeRIP-seq:(Medium) rs111791241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2569,RMVar_hsa_circ_86124,RMVar_hsa_circ_127254,RMVar_hsa_circ_138806,RMVar_hsa_circ_138807,RMVar_hsa_circ_138809,RMVar_hsa_circ_295982 76312 RMVar_ID_76312 Human_SNP_ID_46074118 m1A Human chr1 + 201490326 201490326 201490326 CCTCACCATGCACGGCCACAGTGGTACTGTCCAGATTCTTCTTGCAGACCACTGTGGAGGGGAAG CCTCACCATGCACGGCCACAGTGGTACTGTCCGGATTCTTCTTGCAGACCACTGTGGAGGGGAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201490139..201490393 26863196 MeRIP-seq:(Medium) rs372379780 Functional Loss SNV dbSNP153 33..33 33 - - - 76313 RMVar_ID_76313 Human_SNP_ID_46074922 m1A Human chr1 + 201494072 201494072 201494072 GCGTGACCTGAGACTGCTTCCTGCGGCTGCTCATTGCATAACACCCCCGCACCCCGCCAAGAGCC GCGTGACCTGAGACTGCTTCCTGCGGCTGCTCTTTGCATAACACCCCCGCACCCCGCCAAGAGCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201494070..201494211 26863196 MeRIP-seq:(Medium) rs1330473835 Functional Loss SNV dbSNP153 33..33 33 - - - 76314 RMVar_ID_76314 Human_SNP_ID_46077591 m1A Human chr1 - 201505440 201505440 201505440 TGCAATTGGCCTGCTAATAAAATGGGAAAAACAGGGGTGCTGTGGCCTATTTGCCTGTGGTCTGT TGCAATTGGCCTGCTAATAAAATGGGAAAAACCGGGGTGCTGTGGCCTATTTGCCTGTGGTCTGT T G CSRP1 Ensembl:ENSG00000159176 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201505438..201505611 26863196 MeRIP-seq:(Medium) rs1238438352 Functional Loss SNV dbSNP153 33..33 33 - - - 76315 RMVar_ID_76315 Human_SNP_ID_46077951 m1A Human chr1 - 201507016 201507016 201507016 CGGCTCTGCCCGCCGCGGAGGGGCGCCTGGGCACGCACTCAGCGCCTCCCGGTCTTGCCAGCCCC CGGCTCTGCCCGCCGCGGAGGGGCGCCTGGGCCCGCACTCAGCGCCTCCCGGTCTTGCCAGCCCC T G CSRP1 Ensembl:ENSG00000159176 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201507014..201507125 26863196 MeRIP-seq:(Medium) rs1280517946 Functional Loss SNV dbSNP153 33..33 33 - - - 76316 RMVar_ID_76316 Human_SNP_ID_46078029 m1A Human chr1 - 201507317 201507317 201507317 CGCACAGTGGGACCGCAGCACGAGCTCGGAGCACCCCCAGAGTCGGCGACTCCTGCCCCCGCCCC CGCACAGTGGGACCGCAGCACGAGCTCGGAGCCCCCCCAGAGTCGGCGACTCCTGCCCCCGCCCC T G CSRP1 Ensembl:ENSG00000159176 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:201507276..201507361;chr1:201507267..201507411 26863196 MeRIP-seq:(Medium) rs994501427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_172872,Human_Splice_Rec_172898 76317 RMVar_ID_76317 Human_SNP_ID_46083765 m1A Human chr1 - 201531574 201531574 201531574 TGGGGGTGCCCTGGAGCTGAGCAGCAACAAGGACCGGAGGAGTCAAAGAGAACTGAGGCAGGGAG TGGGGGTGCCCTGGAGCTGAGCAGCAACAAGGGCCGGAGGAGTCAAAGAGAACTGAGGCAGGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201531539..201531634 26863196 MeRIP-seq:(Medium) rs1166659111 Functional Loss SNV dbSNP153 33..33 33 - - - 76318 RMVar_ID_76318 Human_SNP_ID_46110644 m1A Human chr1 - 201643151 201643130 201643151 GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAGAGAGGAAGGAAGGAAGGGAAAGAAGGAAGGAAG GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAG_____________________GAAGGAAGGAAG CTTTCCCTTCCTTCCTTCCTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:201643148..201643373 26863196 MeRIP-seq:(Medium) rs1216427346 Functional Loss DEL dbSNP153 33..53 33 - - - 76319 RMVar_ID_76319 Human_SNP_ID_46110649 m1A Human chr1 - 201643151 201643147 201643151 GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAGAGAGGAAGGAAGGAAGGGAAAGAAGGAAGGAAG GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAG____GAAGGAAGGAAGGGAAAGAAGGAAGGAAG CCTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:201643148..201643373 26863196 MeRIP-seq:(Medium) rs144040451 Functional Loss DEL dbSNP153 33..36 33 - - - 76320 RMVar_ID_76320 Human_SNP_ID_46110650 m1A Human chr1 - 201643151 201643147 201643151 GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAGAGAGGAAGGAAGGAAGGGAAAGAAGGAAGGAAG GAGAAGGAAGGGAAGAAAGGGAAGAAAGAGAG__AGGAAGGAAGGAAGGGAAAGAAGGAAGGAAG CCTCT CCT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:201643148..201643373 26863196 MeRIP-seq:(Medium) rs144040451 Functional Loss DEL dbSNP153 33..34 33 - - - 76321 RMVar_ID_76321 Human_SNP_ID_46110680 m1A Human chr1 - 201643229 201643226 201643230 GAAGGAGGGAGGAAGGAAGGAAAGAAAGAAAGAAAAGGGAAGAGAAGGAAGGGAAGGAAGGAGGA GAAGGAGGGAGGAAGGAAGGAAAGAAAGAAA____AGGGAAGAGAAGGAAGGGAAGGAAGGAGGA TTTTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201643061..201643406 26863196 MeRIP-seq:(Medium) rs369019049 Functional Loss DEL dbSNP153 32..35 33 - - - 76322 RMVar_ID_76322 Human_SNP_ID_46110681 m1A Human chr1 - 201643229 201643228 201643230 GAAGGAGGGAGGAAGGAAGGAAAGAAAGAAAGAAAAGGGAAGAGAAGGAAGGGAAGGAAGGAGGA GAAGGAGGGAGGAAGGAAGGAAAGAAAGAAA__AAAGGGAAGAGAAGGAAGGGAAGGAAGGAGGA TTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201643061..201643406 26863196 MeRIP-seq:(Medium) rs1260648858 Functional Loss DEL dbSNP153 32..33 33 - - - 76323 RMVar_ID_76323 Human_SNP_ID_46111916 m1A Human chr1 - 201648464 201648464 201648464 GGCAAGCCGAGGGCGCAGGGGAAAGAAACGCGAGGAAGGAAGCCGGGAAAAAGGAAAGAGCAGGG GGCAAGCCGAGGGCGCAGGGGAAAGAAACGCGGGGAAGGAAGCCGGGAAAAAGGAAAGAGCAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201648417..201648557 26863196 MeRIP-seq:(Medium) rs1423258375 Functional Loss SNV dbSNP153 33..33 33 - - - 76324 RMVar_ID_76324 Human_SNP_ID_46111922 m1A Human chr1 - 201648480 201648480 201648480 AGGGAGGAGGGAGAGAGGCAAGCCGAGGGCGCAGGGGAAAGAAACGCGAGGAAGGAAGCCGGGAA AGGGAGGAGGGAGAGAGGCAAGCCGAGGGCGCGGGGGAAAGAAACGCGAGGAAGGAAGCCGGGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:201648445..201648552;chr1:201648431..201648552 26863196 MeRIP-seq:(Medium) rs889257828 Functional Loss SNV dbSNP153 33..33 33 - - - 76325 RMVar_ID_76325 Human_SNP_ID_46117435 m1A Human chr1 + 201670726 201670724 201670727 ATGCTGGTGGTGTCTCGGTAATGCTGGTAGAGATGATGGTGATGTTTTGGTGATGGTGGTGGAGA ATGCTGGTGGTGTCTCGGTAATGCTGGTAGA___GATGGTGATGTTTTGGTGATGGTGGTGGAGA AGAT A NAV1 Ensembl:ENSG00000134369 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201670724..201670863 26863196 MeRIP-seq:(Medium) rs1409275383 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_326397 76326 RMVar_ID_76326 Human_SNP_ID_46117467 m1A Human chr1 - 201670864 201670864 201670864 ATCACCATCATCTCTACCACCATCACCAAGATACCACCAGCATCTCTACCACCATTACCAAAACA ATCACCATCATCTCTACCACCATCACCAAGATTCCACCAGCATCTCTACCACCATTACCAAAACA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201670736..201670928 26863196 MeRIP-seq:(Medium) rs1172619573 Functional Loss SNV dbSNP153 33..33 33 - - - 76327 RMVar_ID_76327 Human_SNP_ID_46151823 m1A Human chr1 + 201820104 201820104 201820104 GAGGGACAGGTTCTTGGTGCTGTACCTTTGAGAACTTCCTAGGAAGGAATGGTGGGGTGGCGTTT GAGGGACAGGTTCTTGGTGCTGTACCTTTGAGGACTTCCTAGGAAGGAATGGTGGGGTGGCGTTT A G NAV1 Ensembl:ENSG00000134369 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:201817300..201820552 32194978 MeRIP-seq:(Medium) rs1378481949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4016627 Human_miRNA_ID_1527183,Human_miRNA_ID_1536518,Human_miRNA_ID_2568849 RMVar_hsa_circ_80508,RMVar_hsa_circ_116046,RMVar_hsa_circ_138819,RMVar_hsa_circ_138821,RMVar_hsa_circ_103975,RMVar_hsa_circ_138830,RMVar_hsa_circ_120670,RMVar_hsa_circ_138836 76328 RMVar_ID_76328 Human_SNP_ID_46153859 m1A Human chr1 + 201829227 201829227 201829227 CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCAGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCCGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT A C IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:201829151..201829563;chr1:201829140..201829510 26863196 MeRIP-seq:(Medium) rs1042568436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223155,Human_RBP_ID_744423,Human_RBP_ID_803537,Human_RBP_ID_4016664,Human_RBP_ID_9320307,Human_RBP_ID_18415128 Human_miRNA_ID_2240141,Human_miRNA_ID_2576970 RMVar_hsa_circ_84187,RMVar_hsa_circ_138839 76329 RMVar_ID_76329 Human_SNP_ID_46153860 m1A Human chr1 + 201829227 201829227 201829227 CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCAGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCGGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT A G IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:201829151..201829563;chr1:201829140..201829510 26863196 MeRIP-seq:(Medium) rs1042568436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223155,Human_RBP_ID_744423,Human_RBP_ID_803537,Human_RBP_ID_4016664,Human_RBP_ID_9320307,Human_RBP_ID_18415128 Human_miRNA_ID_2240141,Human_miRNA_ID_2576970 RMVar_hsa_circ_84187,RMVar_hsa_circ_138839 76330 RMVar_ID_76330 Human_SNP_ID_46153863 m1A Human chr1 - 201829230 201829230 201829230 GCCACTGGACCCGGCAGCCCGGAGGCCGCACCAGCTGCCGCCGCCGCCGCCATCTTTTCTCCCCT GCCACTGGACCCGGCAGCCCGGAGGCCGCACCGGCTGCCGCCGCCGCCGCCATCTTTTCTCCCCT T C IPO9-AS1 Ensembl:ENSG00000231871 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:201829151..201829560 26863196 MeRIP-seq:(Medium) rs763421015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245433 76331 RMVar_ID_76331 Human_SNP_ID_46153864 m1A Human chr1 - 201829230 201829230 201829230 GCCACTGGACCCGGCAGCCCGGAGGCCGCACCAGCTGCCGCCGCCGCCGCCATCTTTTCTCCCCT GCCACTGGACCCGGCAGCCCGGAGGCCGCACCCGCTGCCGCCGCCGCCGCCATCTTTTCTCCCCT T G IPO9-AS1 Ensembl:ENSG00000231871 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:201829151..201829560 26863196 MeRIP-seq:(Medium) rs763421015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245433 76332 RMVar_ID_76332 Human_SNP_ID_46153900 m1A Human chr1 - 201829283 201829283 201829283 CTGGGGATAGGATCCCGGTGAGCGTATCCACTAACGCTTCCTTTAATCCTTGTGCCACTGGACCC CTGGGGATAGGATCCCGGTGAGCGTATCCACTGACGCTTCCTTTAATCCTTGTGCCACTGGACCC T C IPO9-AS1 Ensembl:ENSG00000231871 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:201829215..201829314 32194978 MeRIP-seq:(Medium) rs201579189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245433,Human_RBP_ID_18559787 76333 RMVar_ID_76333 Human_SNP_ID_46158473 m1A Human chr1 + 201848526 201848526 201848526 GGACTGGCCTGAAGCTTGGCCCCAACTCTTCAACCTGCTCATGGAGATGTTGGTGAGCGGAGACT GGACTGGCCTGAAGCTTGGCCCCAACTCTTCAGCCTGCTCATGGAGATGTTGGTGAGCGGAGACT A G IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:201848476..201850452 32194978 MeRIP-seq:(Medium) rs766228383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337609,Human_RBP_ID_8754304,Human_RBP_ID_8961106,Human_RBP_ID_10724436,Human_RBP_ID_18969420 Human_Splice_Rec_173281,Human_Splice_Rec_173291,Human_Splice_Rec_173333 RMVar_hsa_circ_116048,RMVar_hsa_circ_284083,RMVar_hsa_circ_311525,RMVar_hsa_circ_323536,RMVar_hsa_circ_328106,RMVar_hsa_circ_346557,RMVar_hsa_circ_282144,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_79439,RMVar_hsa_circ_91487,RMVar_hsa_circ_103662,RMVar_hsa_circ_86734,RMVar_hsa_circ_138846,RMVar_hsa_circ_138848,RMVar_hsa_circ_138847,RMVar_hsa_circ_138844,RMVar_hsa_circ_138845,RMVar_hsa_circ_138843,RMVar_hsa_circ_15129,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_138851 76334 RMVar_ID_76334 Human_SNP_ID_46159524 m1A Human chr1 + 201853056 201853056 201853056 GAACCCGTTCCCGAGCCGTGGAGATTTTTACCACTTGTGCCCATATGATCTGTAACATGGAGGAG GAACCCGTTCCCGAGCCGTGGAGATTTTTACCGCTTGTGCCCATATGATCTGTAACATGGAGGAG A G IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:201852187..201854860 32194978 MeRIP-seq:(Medium) rs1558219337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973822,Human_RBP_ID_1418599,Human_RBP_ID_1733170,Human_RBP_ID_3937141,Human_RBP_ID_4016705,Human_RBP_ID_5338787,Human_RBP_ID_5537125,Human_RBP_ID_8755282,Human_RBP_ID_9271696,Human_RBP_ID_10724621,Human_RBP_ID_18174590,Human_RBP_ID_18559816,Human_RBP_ID_18966308,Human_RBP_ID_22637928 Human_Splice_Rec_173284,Human_Splice_Rec_173294,Human_Splice_Rec_173295 RMVar_hsa_circ_21645,RMVar_hsa_circ_116048,RMVar_hsa_circ_284083,RMVar_hsa_circ_311525,RMVar_hsa_circ_328106,RMVar_hsa_circ_346557,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_79439,RMVar_hsa_circ_91487,RMVar_hsa_circ_103662,RMVar_hsa_circ_86734,RMVar_hsa_circ_138846,RMVar_hsa_circ_138847,RMVar_hsa_circ_138844,RMVar_hsa_circ_138845,RMVar_hsa_circ_138843,RMVar_hsa_circ_15129,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_127013,RMVar_hsa_circ_275089,RMVar_hsa_circ_314641,RMVar_hsa_circ_371045,RMVar_hsa_circ_138851,RMVar_hsa_circ_347770,RMVar_hsa_circ_280494,RMVar_hsa_circ_271966,RMVar_hsa_circ_84204,RMVar_hsa_circ_24144,RMVar_hsa_circ_138854,RMVar_hsa_circ_138856,RMVar_hsa_circ_138858,RMVar_hsa_circ_138857,RMVar_hsa_circ_138855,RMVar_hsa_circ_138852,RMVar_hsa_circ_138853,RMVar_hsa_circ_138861,RMVar_hsa_circ_303706,RMVar_hsa_circ_360500,RMVar_hsa_circ_101459,RMVar_hsa_circ_138860 76335 RMVar_ID_76335 Human_SNP_ID_46163044 m1A Human chr1 + 201866820 201866820 201866820 CCCAGCATCCTTGATGGCTTAATTCACCTAGCAGCCCAGTTCAGCTCAGAGGTCCTCAACCTGGT CCCAGCATCCTTGATGGCTTAATTCACCTAGCGGCCCAGTTCAGCTCAGAGGTCCTCAACCTGGT A G IPO9 Ensembl:ENSG00000198700 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201866773..201866999 26863196 MeRIP-seq:(Medium) rs1176874100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23746,Human_RBP_ID_8961121,Human_RBP_ID_10725136,Human_RBP_ID_21880842 Human_Splice_Rec_173310 Human_miRNA_ID_1156600,Human_miRNA_ID_2552450 RMVar_hsa_circ_21645,RMVar_hsa_circ_116048,RMVar_hsa_circ_311525,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_103662,RMVar_hsa_circ_86734,RMVar_hsa_circ_138843,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_371045,RMVar_hsa_circ_138851,RMVar_hsa_circ_347770,RMVar_hsa_circ_280494,RMVar_hsa_circ_84204,RMVar_hsa_circ_138854,RMVar_hsa_circ_138852,RMVar_hsa_circ_138853,RMVar_hsa_circ_109155,RMVar_hsa_circ_119239,RMVar_hsa_circ_32084,RMVar_hsa_circ_138862,RMVar_hsa_circ_138863,RMVar_hsa_circ_79036,RMVar_hsa_circ_138867,RMVar_hsa_circ_67495,RMVar_hsa_circ_79743,RMVar_hsa_circ_265825,RMVar_hsa_circ_313495,RMVar_hsa_circ_277355,RMVar_hsa_circ_127663,RMVar_hsa_circ_138873,RMVar_hsa_circ_49404,RMVar_hsa_circ_138871,RMVar_hsa_circ_138872,RMVar_hsa_circ_102628,RMVar_hsa_circ_127904,RMVar_hsa_circ_105549,RMVar_hsa_circ_110160,RMVar_hsa_circ_138877,RMVar_hsa_circ_138879,RMVar_hsa_circ_138880,RMVar_hsa_circ_319689,RMVar_hsa_circ_138883,RMVar_hsa_circ_88983,RMVar_hsa_circ_92049,RMVar_hsa_circ_138884,RMVar_hsa_circ_138882,RMVar_hsa_circ_360726 76336 RMVar_ID_76336 Human_SNP_ID_46163064 m1A Human chr1 + 201866880 201866880 201866880 CTGGTGATGGAGACCCTGTGCATCGTTTGTACAGTAGACCCCGAATTCACAGCAAGCATGGAAAG CTGGTGATGGAGACCCTGTGCATCGTTTGTACGGTAGACCCCGAATTCACAGCAAGCATGGAAAG A G IPO9 Ensembl:ENSG00000198700 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:201866726..201866975 26863196 MeRIP-seq:(Medium) rs370074232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23747,Human_RBP_ID_273407,Human_RBP_ID_337621,Human_RBP_ID_804343,Human_RBP_ID_1418624,Human_RBP_ID_1733199,Human_RBP_ID_3292445,Human_RBP_ID_4016737,Human_RBP_ID_5544858,Human_RBP_ID_8240426,Human_RBP_ID_10725137,Human_RBP_ID_18559849,Human_RBP_ID_21879401,Human_RBP_ID_22852447,Human_RBP_ID_26849957 Human_Splice_Rec_173311 RMVar_hsa_circ_21645,RMVar_hsa_circ_116048,RMVar_hsa_circ_311525,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_103662,RMVar_hsa_circ_86734,RMVar_hsa_circ_138843,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_371045,RMVar_hsa_circ_138851,RMVar_hsa_circ_347770,RMVar_hsa_circ_280494,RMVar_hsa_circ_84204,RMVar_hsa_circ_138854,RMVar_hsa_circ_138852,RMVar_hsa_circ_138853,RMVar_hsa_circ_109155,RMVar_hsa_circ_119239,RMVar_hsa_circ_32084,RMVar_hsa_circ_138862,RMVar_hsa_circ_138863,RMVar_hsa_circ_79036,RMVar_hsa_circ_138867,RMVar_hsa_circ_67495,RMVar_hsa_circ_79743,RMVar_hsa_circ_265825,RMVar_hsa_circ_313495,RMVar_hsa_circ_277355,RMVar_hsa_circ_127663,RMVar_hsa_circ_138873,RMVar_hsa_circ_49404,RMVar_hsa_circ_138871,RMVar_hsa_circ_138872,RMVar_hsa_circ_102628,RMVar_hsa_circ_127904,RMVar_hsa_circ_105549,RMVar_hsa_circ_110160,RMVar_hsa_circ_138877,RMVar_hsa_circ_138879,RMVar_hsa_circ_138880,RMVar_hsa_circ_319689,RMVar_hsa_circ_138883,RMVar_hsa_circ_88983,RMVar_hsa_circ_92049,RMVar_hsa_circ_138884,RMVar_hsa_circ_138882,RMVar_hsa_circ_360726 76337 RMVar_ID_76337 Human_SNP_ID_46163450 m1A Human chr1 + 201868592 201868592 201868592 GGTTAGGGCCAAACAACAGGCATCATTAAGCGAGAAGCAGATGCAGACCATCAGGCAGGGGGATT GGTTAGGGCCAAACAACAGGCATCATTAAGCGGGAAGCAGATGCAGACCATCAGGCAGGGGGATT A G IPO9 Ensembl:ENSG00000198700 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201868588..201868815 26863196 MeRIP-seq:(Medium) rs1227519075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10725236 RMVar_hsa_circ_21645,RMVar_hsa_circ_116048,RMVar_hsa_circ_311525,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_103662,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_371045,RMVar_hsa_circ_138851,RMVar_hsa_circ_347770,RMVar_hsa_circ_280494,RMVar_hsa_circ_84204,RMVar_hsa_circ_138854,RMVar_hsa_circ_138852,RMVar_hsa_circ_138853,RMVar_hsa_circ_109155,RMVar_hsa_circ_119239,RMVar_hsa_circ_32084,RMVar_hsa_circ_138862,RMVar_hsa_circ_138863,RMVar_hsa_circ_79036,RMVar_hsa_circ_138867,RMVar_hsa_circ_79743,RMVar_hsa_circ_265825,RMVar_hsa_circ_313495,RMVar_hsa_circ_277355,RMVar_hsa_circ_127663,RMVar_hsa_circ_138873,RMVar_hsa_circ_49404,RMVar_hsa_circ_138871,RMVar_hsa_circ_138872,RMVar_hsa_circ_127904,RMVar_hsa_circ_105549,RMVar_hsa_circ_138880,RMVar_hsa_circ_319689,RMVar_hsa_circ_138883,RMVar_hsa_circ_88983,RMVar_hsa_circ_92049,RMVar_hsa_circ_138884,RMVar_hsa_circ_138882,RMVar_hsa_circ_360726 76338 RMVar_ID_76338 Human_SNP_ID_46163732 m1A Human chr1 + 201869629 201869629 201869629 TTGATATCCTGACAACAGTAGTACGAAATACAAAGCCTCCCCTTTCCCAGCTTCTCATCTGCCAA TTGATATCCTGACAACAGTAGTACGAAATACAGAGCCTCCCCTTTCCCAGCTTCTCATCTGCCAA A G IPO9 Ensembl:ENSG00000198700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:201857169..201869629 32194978 MeRIP-seq:(Medium) rs151254389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23751,Human_RBP_ID_850726,Human_RBP_ID_1733205,Human_RBP_ID_17223015,Human_RBP_ID_19152492,Human_RBP_ID_24622823,Human_RBP_ID_26309876 Human_Splice_Rec_173314,Human_Splice_Rec_173315 RMVar_hsa_circ_116048,RMVar_hsa_circ_311525,RMVar_hsa_circ_127270,RMVar_hsa_circ_138842,RMVar_hsa_circ_103662,RMVar_hsa_circ_138840,RMVar_hsa_circ_138841,RMVar_hsa_circ_90397,RMVar_hsa_circ_371045,RMVar_hsa_circ_138851,RMVar_hsa_circ_347770,RMVar_hsa_circ_280494,RMVar_hsa_circ_84204,RMVar_hsa_circ_138854,RMVar_hsa_circ_138852,RMVar_hsa_circ_138853,RMVar_hsa_circ_109155,RMVar_hsa_circ_119239,RMVar_hsa_circ_32084,RMVar_hsa_circ_138862,RMVar_hsa_circ_138863,RMVar_hsa_circ_79036,RMVar_hsa_circ_138867,RMVar_hsa_circ_79743,RMVar_hsa_circ_265825,RMVar_hsa_circ_277355,RMVar_hsa_circ_127663,RMVar_hsa_circ_138873,RMVar_hsa_circ_49404,RMVar_hsa_circ_138871,RMVar_hsa_circ_138872,RMVar_hsa_circ_41874,RMVar_hsa_circ_105549,RMVar_hsa_circ_138880,RMVar_hsa_circ_319689,RMVar_hsa_circ_138883,RMVar_hsa_circ_88983,RMVar_hsa_circ_92049,RMVar_hsa_circ_138884,RMVar_hsa_circ_118446,RMVar_hsa_circ_347872,RMVar_hsa_circ_138885 76339 RMVar_ID_76339 Human_SNP_ID_46165866 m1A Human chr1 + 201877453 201877453 201877453 TGAACTTGGGAAGCAGAGGTTGCAGTGAACCGATATCACACCGTTGCATTCCAAGGCAAGACTCA TGAACTTGGGAAGCAGAGGTTGCAGTGAACCGCTATCACACCGTTGCATTCCAAGGCAAGACTCA A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1433822926 Functional Loss SNV dbSNP153 33..33 33 - - - 76340 RMVar_ID_76340 Human_SNP_ID_46168802 m1A Human chr1 - 201888743 201888743 201888743 TCTGGAGCTGGGTGCCCCTCACCCAGCAGAGCACTGCCCTGCTCCCCCTGTCCCCGGCTCCGCGG TCTGGAGCTGGGTGCCCCTCACCCAGCAGAGCCCTGCCCTGCTCCCCCTGTCCCCGGCTCCGCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201888694..201888858 26863196 MeRIP-seq:(Medium) rs1055013175 Functional Loss SNV dbSNP153 33..33 33 - - - 76341 RMVar_ID_76341 Human_SNP_ID_46169570 m1A Human chr1 + 201891455 201891455 201891455 CATCCCAGTGCAGCCAGTATACCCATACCCCCAGGACCCCAAAGCTGGCCCTGCACCCCCACAGC CATCCCAGTGCAGCCAGTATACCCATACCCCCGGGACCCCAAAGCTGGCCCTGCACCCCCACAGC A G SHISA4 Ensembl:ENSG00000198892 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201891388..201891909 26863196 MeRIP-seq:(Medium) rs773137841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_173346,Human_Splice_Rec_173354 RMVar_hsa_circ_109019,RMVar_hsa_circ_138889 76342 RMVar_ID_76342 Human_SNP_ID_46186668 m1A Human chr1 + 201955546 201955546 201955546 CATTGGAGTCAAGATGGAGGAGTACGCGCGAGAGCCTTGGTGAGCTTCACCGCTGTCTTTGCATT CATTGGAGTCAAGATGGAGGAGTACGCGCGAGGGCCTTGGTGAGCTTCACCGCTGTCTTTGCATT A G TIMM17A Ensembl:ENSG00000134375 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:201955501..201955661 26863196 MeRIP-seq:(Medium) rs1316423033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10726146,Human_RBP_ID_19039962,Human_RBP_ID_22431208,Human_RBP_ID_22871467 Human_Splice_Rec_173371,Human_Splice_Rec_173381,Human_Splice_Rec_173393 RMVar_hsa_circ_126321,RMVar_hsa_circ_138890 76343 RMVar_ID_76343 Human_SNP_ID_46187149 m1A Human chr1 - 201957257 201957257 201957257 CGCCATGGGCTAAGAACAGGGGGAAAAAAAAGACCATATTTCTCATTCACAAACCATAAAATCTT CGCCATGGGCTAAGAACAGGGGGAAAAAAAAGGCCATATTTCTCATTCACAAACCATAAAATCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201957253..201957575 26863196 MeRIP-seq:(Medium) rs201877659 Functional Loss SNV dbSNP153 33..33 33 - - - 76344 RMVar_ID_76344 Human_SNP_ID_46188909 m1A Human chr1 + 201963569 201963569 201963569 TATGTTTTTGACTATAATATTTTAAATGGAAGATGAAATTTAAATTAGTATTTGCTTGTTTCTTT TATGTTTTTGACTATAATATTTTAAATGGAAGGTGAAATTTAAATTAGTATTTGCTTGTTTCTTT A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201963566..201963785 26863196 MeRIP-seq:(Medium) rs1558250896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17590246,Human_RBP_ID_22634826 RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 76345 RMVar_ID_76345 Human_SNP_ID_46188914 m1A Human chr1 - 201963582 201963582 201963582 TATTTTATTGTAAAAAGAAACAAGCAAATACTAATTTAAATTTCATCTTCCATTTAAAATATTAT TATTTTATTGTAAAAAGAAACAAGCAAATACTGATTTAAATTTCATCTTCCATTTAAAATATTAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201963579..201963750 26863196 MeRIP-seq:(Medium) rs761079659 Functional Loss SNV dbSNP153 33..33 33 - - - 76346 RMVar_ID_76346 Human_SNP_ID_46188926 m1A Human chr1 + 201963609 201963609 201963609 TAAATTAGTATTTGCTTGTTTCTTTTTACAATAAAATAGGTAGCTTTGCAGTTTGGGGAGGGCTG TAAATTAGTATTTGCTTGTTTCTTTTTACAATCAAATAGGTAGCTTTGCAGTTTGGGGAGGGCTG A C TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201963601..201963650 26863196 MeRIP-seq:(Medium) rs201710712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5739387,Human_RBP_ID_22634826,Human_RBP_ID_23355756 RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 76347 RMVar_ID_76347 Human_SNP_ID_46193984 m1A Human chr1 - 201982684 201982684 201982684 AGCGGCCGCCGGGCCGCGCCGCTGCCGGGGGAATGCTCGCCGCTCGCCATGGCCGCAGAGCCGTT AGCGGCCGCCGGGCCGCGCCGCTGCCGGGGGAGTGCTCGCCGCTCGCCATGGCCGCAGAGCCGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201982626..201983100 26863196 MeRIP-seq:(Medium) rs1041815549 Functional Loss SNV dbSNP153 33..33 33 - - - 76348 RMVar_ID_76348 Human_SNP_ID_46193996 m1A Human chr1 + 201982694 201982694 201982694 CGGCCATGGCGAGCGGCGAGCATTCCCCCGGCAGCGGCGCGGCCCGGCGGCCGCTGCACTCCGCG CGGCCATGGCGAGCGGCGAGCATTCCCCCGGCCGCGGCGCGGCCCGGCGGCCGCTGCACTCCGCG A C RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:201982651..201982886;chr1:201982651..201982917 26863196 MeRIP-seq:(Medium) rs1558256553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337757,Human_RBP_ID_4073224,Human_RBP_ID_17735456 RMVar_hsa_circ_265446 76349 RMVar_ID_76349 Human_SNP_ID_46197944 m1A Human chr1 + 201997426 201997426 201997426 CTGCCTGCTAGCTGGGGACCGCTCCTTGGCAGATGTCATCATCCATGAGATCTCCCACAGTTGGT CTGCCTGCTAGCTGGGGACCGCTCCTTGGCAGTTGTCATCATCCATGAGATCTCCCACAGTTGGT A T RNPEP Ensembl:ENSG00000176393 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:201997301..201997425 32194978 MeRIP-seq:(Medium) rs1033681386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973849,Human_RBP_ID_3937157,Human_RBP_ID_18187350,Human_RBP_ID_22024092 Human_miRNA_ID_2721117 RMVar_hsa_circ_138892,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_302797,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893,RMVar_hsa_circ_125228,RMVar_hsa_circ_138900,RMVar_hsa_circ_359068,RMVar_hsa_circ_371191,RMVar_hsa_circ_372367,RMVar_hsa_circ_370097,RMVar_hsa_circ_305617,RMVar_hsa_circ_138898,RMVar_hsa_circ_138899,RMVar_hsa_circ_331181,RMVar_hsa_circ_138897,RMVar_hsa_circ_282989,RMVar_hsa_circ_138901,RMVar_hsa_circ_138902,RMVar_hsa_circ_138903 76350 RMVar_ID_76350 Human_SNP_ID_46198628 m1A Human chr1 + 201999953 201999953 201999953 GGAGGCTGCAACGGGGCGGGCTCTGCTGCGTCAGCACATGGACATCACTGGAGAGGAAAACCCAC GGAGGCTGCAACGGGGCGGGCTCTGCTGCGTCCGCACATGGACATCACTGGAGAGGAAAACCCAC A C RNPEP Ensembl:ENSG00000176393 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:201999903..202000039 26863196 MeRIP-seq:(Medium) rs1206248311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8295077,Human_RBP_ID_19253361 Human_Splice_Rec_173410,Human_Splice_Rec_173411,Human_Splice_Rec_173422,Human_Splice_Rec_173423,Human_Splice_Rec_173440,Human_Splice_Rec_173441,Human_Splice_Rec_173462,Human_Splice_Rec_173463,Human_Splice_Rec_173472,Human_Splice_Rec_173473,Human_Splice_Rec_173492,Human_Splice_Rec_173493,Human_Splice_Rec_173504,Human_Splice_Rec_173505,Human_Splice_Rec_173518,Human_Splice_Rec_173526,Human_Splice_Rec_173527 Human_miRNA_ID_2948302 RMVar_hsa_circ_26345,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893,RMVar_hsa_circ_125228,RMVar_hsa_circ_359068,RMVar_hsa_circ_371191,RMVar_hsa_circ_372367,RMVar_hsa_circ_370097,RMVar_hsa_circ_138898,RMVar_hsa_circ_138899,RMVar_hsa_circ_138897,RMVar_hsa_circ_282989,RMVar_hsa_circ_138902,RMVar_hsa_circ_138903,RMVar_hsa_circ_268698,RMVar_hsa_circ_294942,RMVar_hsa_circ_111561,RMVar_hsa_circ_138904,RMVar_hsa_circ_138905 76351 RMVar_ID_76351 Human_SNP_ID_46202883 m1A Human chr1 - 202015256 202015256 202015256 AGCCGCTTGAGTTTTTGCCAAACTTGTAGACGAGTCGCCGGCCATCCACCCGTTCCAGGATCTCC AGCCGCTTGAGTTTTTGCCAAACTTGTAGACGCGTCGCCGGCCATCCACCCGTTCCAGGATCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:202015217..202015298 26863196 MeRIP-seq:(Medium) rs1458867390 Functional Loss SNV dbSNP153 33..33 33 - - - 76352 RMVar_ID_76352 Human_SNP_ID_46236078 m1A Human chr1 - 202144659 202144659 202144659 CCGCCCGCACCGAGCCGCGGGACCCGGGCCGTACCGGGGAGGGGCCGCTCCGGGCCGCAGCGCGA CCGCCCGCACCGAGCCGCGGGACCCGGGCCGTGCCGGGGAGGGGCCGCTCCGGGCCGCAGCGCGA T C ARL8A Ensembl:ENSG00000143862 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:202144476..202144725 26863196 MeRIP-seq:(Medium) rs1180438549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4087132 76353 RMVar_ID_76353 Human_SNP_ID_46236092 m1A Human chr1 - 202144707 202144707 202144707 GCGAGCCGATTCCGGGGCAGCGAGTCGTCGGCAGCCGCGCTCGAGCCTCCGCCCGCACCGAGCCG GCGAGCCGATTCCGGGGCAGCGAGTCGTCGGCTGCCGCGCTCGAGCCTCCGCCCGCACCGAGCCG T A ARL8A Ensembl:ENSG00000143862 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4989100 Functional Loss SNV dbSNP153 33..33 33 - - - 76354 RMVar_ID_76354 Human_SNP_ID_46236093 m1A Human chr1 - 202144707 202144707 202144707 GCGAGCCGATTCCGGGGCAGCGAGTCGTCGGCAGCCGCGCTCGAGCCTCCGCCCGCACCGAGCCG GCGAGCCGATTCCGGGGCAGCGAGTCGTCGGCCGCCGCGCTCGAGCCTCCGCCCGCACCGAGCCG T G ARL8A Ensembl:ENSG00000143862 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4989100 Functional Loss SNV dbSNP153 33..33 33 - - - 76355 RMVar_ID_76355 Human_SNP_ID_46286977 m1A Human chr1 - 202341019 202341019 202341019 AACCTTTAATATCTAAAGGTGTGAAAGAATAAAACTTTTATGGGCAGCAGGAATAGTGCAGTGTG AACCTTTAATATCTAAAGGTGTGAAAGAATAACACTTTTATGGGCAGCAGGAATAGTGCAGTGTG T G UBE2T Ensembl:ENSG00000077152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:202341006..202341156 26863196 MeRIP-seq:(Medium) rs1319916614 Functional Loss SNV dbSNP153 33..33 33 - - - 76356 RMVar_ID_76356 Human_SNP_ID_46287206 m1A Human chr1 - 202341820 202341820 202341820 ACACTGGAGAAGGTCACTGAGTCTTGGGGGGAAGGAGTCCTGTTTCCGCCTAATATGGGAGTTTT ACACTGGAGAAGGTCACTGAGTCTTGGGGGGAGGGAGTCCTGTTTCCGCCTAATATGGGAGTTTT T C UBE2T Ensembl:ENSG00000077152 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:202341818..202341906 26863196 MeRIP-seq:(Medium) rs1350985505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223574,Human_RBP_ID_10727540 76357 RMVar_ID_76357 Human_SNP_ID_46288722 m1A Human chr1 - 202348770 202348770 202348770 TTGGGGCTCGAGTTGCCGCTGCCGCCTCTCTCAGAGCGCTTCAGCCCGGAGCAGAGGGCGGAGAC TTGGGGCTCGAGTTGCCGCTGCCGCCTCTCTCTGAGCGCTTCAGCCCGGAGCAGAGGGCGGAGAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:202348720..202349006 26863196 MeRIP-seq:(Medium) rs895179933 Functional Loss SNV dbSNP153 33..33 33 - - - 76358 RMVar_ID_76358 Human_SNP_ID_46373721 m1A Human chr1 - 202730926 202730926 202730926 CTGCTCAGCAGACTGACCGAAGCTCACCAGTGAGACCCAGCAGTGAGAAGGTGAGTGTCTGAGAG CTGCTCAGCAGACTGACCGAAGCTCACCAGTGGGACCCAGCAGTGAGAAGGTGAGTGTCTGAGAG T C KDM5B Ensembl:ENSG00000117139 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202730909..202731974 32194978 MeRIP-seq:(Medium) rs771323194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8755290,Human_RBP_ID_9253103 Human_Splice_Rec_174581,Human_Splice_Rec_174635,Human_Splice_Rec_174641,Human_Splice_Rec_174691,Human_Splice_Rec_174743,Human_Splice_Rec_174761,Human_Splice_Rec_174821,Human_Splice_Rec_174871,Human_Splice_Rec_174923,Human_Splice_Rec_174975,Human_Splice_Rec_174999,Human_Splice_Rec_175017,Human_Splice_Rec_175067,Human_Splice_Rec_175071,Human_Splice_Rec_175119,Human_Splice_Rec_175143,Human_Splice_Rec_175195,Human_Splice_Rec_175203,Human_Splice_Rec_175231,Human_Splice_Rec_175281 RMVar_hsa_circ_28265,RMVar_hsa_circ_101583,RMVar_hsa_circ_117021,RMVar_hsa_circ_119014,RMVar_hsa_circ_105020,RMVar_hsa_circ_138946,RMVar_hsa_circ_78077,RMVar_hsa_circ_87332,RMVar_hsa_circ_138948,RMVar_hsa_circ_138950,RMVar_hsa_circ_138951,RMVar_hsa_circ_138949,RMVar_hsa_circ_138947,RMVar_hsa_circ_113271,RMVar_hsa_circ_121952,RMVar_hsa_circ_265285,RMVar_hsa_circ_89858,RMVar_hsa_circ_138953,RMVar_hsa_circ_138954,RMVar_hsa_circ_265823,RMVar_hsa_circ_138952 76359 RMVar_ID_76359 Human_SNP_ID_46376997 m1A Human chr1 - 202742751 202742751 202742751 AATTGAAGAATCTGAAATGAAGAAATTCCCAGACAATGATCTTTTGCGACACCTTCGCCTAGTCA AATTGAAGAATCTGAAATGAAGAAATTCCCAGGCAATGATCTTTTGCGACACCTTCGCCTAGTCA T C KDM5B Ensembl:ENSG00000117139 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202742700..202742800 32194978 MeRIP-seq:(Medium) rs1472158579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18557,Human_RBP_ID_851938,Human_RBP_ID_3934436,Human_RBP_ID_9253109,Human_RBP_ID_9359742 Human_Splice_Rec_174564,Human_Splice_Rec_174565,Human_Splice_Rec_174618,Human_Splice_Rec_174619,Human_Splice_Rec_174674,Human_Splice_Rec_174675,Human_Splice_Rec_174726,Human_Splice_Rec_174727,Human_Splice_Rec_174746,Human_Splice_Rec_174747,Human_Splice_Rec_174804,Human_Splice_Rec_174805,Human_Splice_Rec_174854,Human_Splice_Rec_174855,Human_Splice_Rec_174906,Human_Splice_Rec_174907,Human_Splice_Rec_174958,Human_Splice_Rec_174959,Human_Splice_Rec_174982,Human_Splice_Rec_174983,Human_Splice_Rec_175003,Human_Splice_Rec_175050,Human_Splice_Rec_175051,Human_Splice_Rec_175102,Human_Splice_Rec_175103,Human_Splice_Rec_175126,Human_Splice_Rec_175127,Human_Splice_Rec_175178,Human_Splice_Rec_175179,Human_Splice_Rec_175214,Human_Splice_Rec_175215,Human_Splice_Rec_175264,Human_Splice_Rec_175265,Human_Splice_Rec_175314,Human_Splice_Rec_175315 RMVar_hsa_circ_101583,RMVar_hsa_circ_119014,RMVar_hsa_circ_105020,RMVar_hsa_circ_138946,RMVar_hsa_circ_78077,RMVar_hsa_circ_87332,RMVar_hsa_circ_138948,RMVar_hsa_circ_138950,RMVar_hsa_circ_138949,RMVar_hsa_circ_138947,RMVar_hsa_circ_113271,RMVar_hsa_circ_89858,RMVar_hsa_circ_17105,RMVar_hsa_circ_115846,RMVar_hsa_circ_77623,RMVar_hsa_circ_124590,RMVar_hsa_circ_138953,RMVar_hsa_circ_138954,RMVar_hsa_circ_120936,RMVar_hsa_circ_138955,RMVar_hsa_circ_138956,RMVar_hsa_circ_138957,RMVar_hsa_circ_269587,RMVar_hsa_circ_120317,RMVar_hsa_circ_9279,RMVar_hsa_circ_50352,RMVar_hsa_circ_138959,RMVar_hsa_circ_100466,RMVar_hsa_circ_138960,RMVar_hsa_circ_138958,RMVar_hsa_circ_310137,RMVar_hsa_circ_369487,RMVar_hsa_circ_100904,RMVar_hsa_circ_138964,RMVar_hsa_circ_85060,RMVar_hsa_circ_138962,RMVar_hsa_circ_138963,RMVar_hsa_circ_101295,RMVar_hsa_circ_138965,RMVar_hsa_circ_83716,RMVar_hsa_circ_308028,RMVar_hsa_circ_321543,RMVar_hsa_circ_344870,RMVar_hsa_circ_308654,RMVar_hsa_circ_92323,RMVar_hsa_circ_20253,RMVar_hsa_circ_113133,RMVar_hsa_circ_138967,RMVar_hsa_circ_138969,RMVar_hsa_circ_138970,RMVar_hsa_circ_138971,RMVar_hsa_circ_138968,RMVar_hsa_circ_138966,RMVar_hsa_circ_26592,RMVar_hsa_circ_58002,RMVar_hsa_circ_138972 76360 RMVar_ID_76360 Human_SNP_ID_46383016 m1A Human chr1 + 202766485 202766485 202766485 CCAAGATCGCGCCACTGCACTCCAGCCTGGGCAACACAGCGAGACTCTGTCTCTAAAAAAAAAAA CCAAGATCGCGCCACTGCACTCCAGCCTGGGCGACACAGCGAGACTCTGTCTCTAAAAAAAAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202766482..202773161 32194978 MeRIP-seq:(Medium) rs1354874224 Functional Loss SNV dbSNP153 33..33 33 - - - 76361 RMVar_ID_76361 Human_SNP_ID_46393993 m1A Human chr1 - 202807914 202807914 202807914 GGGGAGGAAGACGGGGGCTTCTCCAGGGTGGGAGATGAGGAGCGTGGGAGAACCGGGGGCTTCGG GGGGAGGAAGACGGGGGCTTCTCCAGGGTGGGGGATGAGGAGCGTGGGAGAACCGGGGGCTTCGG T C KDM5B Ensembl:ENSG00000117139 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:202807721..202808058 26863196 MeRIP-seq:(Medium) rs372180262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259061,Human_RBP_ID_803593,Human_RBP_ID_3328758,Human_RBP_ID_4073229,Human_RBP_ID_5311935,Human_RBP_ID_8052821,Human_RBP_ID_8167291,Human_RBP_ID_8227857,Human_RBP_ID_9320313,Human_RBP_ID_9410710,Human_RBP_ID_18455718,Human_RBP_ID_18928844 RMVar_hsa_circ_101922,RMVar_hsa_circ_139000 76362 RMVar_ID_76362 Human_SNP_ID_46407556 m1A Human chr1 - 202861365 202861365 202861365 GGGCGCACGGGGGGTCGGTGGGAAGGGCCCGCAGCGCAAAACGGAAGGGCGCCCCGGCAGTCCAG GGGCGCACGGGGGGTCGGTGGGAAGGGCCCGCCGCGCAAAACGGAAGGGCGCCCCGGCAGTCCAG T G AC098934.1 Ensembl:ENSG00000214796 Pseudogene intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:202861282..202861411 26863196 MeRIP-seq:(Medium) rs1271886778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746835,Human_RBP_ID_856374,Human_RBP_ID_3330508,Human_RBP_ID_8171256,Human_RBP_ID_9412669,Human_RBP_ID_18928846,Human_RBP_ID_21963583 76363 RMVar_ID_76363 Human_SNP_ID_46412000 m1A Human chr1 - 202880642 202880642 202880642 GCCCAGGGGCTCCCGCTTTTTCTTGCTCTAGAAGAGCAGTATTCAACCTTTTAGCTATGATGACA GCCCAGGGGCTCCCGCTTTTTCTTGCTCTAGAGGAGCAGTATTCAACCTTTTAGCTATGATGACA T C RABIF Ensembl:ENSG00000183155 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1131905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338013,Human_RBP_ID_18930337 GWAS_ID_9185,GWAS_ID_9186,GWAS_ID_9187,GWAS_ID_9188,GWAS_ID_9189,GWAS_ID_9190,GWAS_ID_9191,GWAS_ID_9192,GWAS_ID_9193,GWAS_ID_9194,GWAS_ID_9195,GWAS_ID_9196,GWAS_ID_9197,GWAS_ID_9198,GWAS_ID_9199,GWAS_ID_9200,GWAS_ID_9201,GWAS_ID_9202,GWAS_ID_9203,GWAS_ID_9204,GWAS_ID_9205,GWAS_ID_9206 76364 RMVar_ID_76364 Human_SNP_ID_46414427 m1A Human chr1 - 202889069 202889069 202889069 GCGATGGAACCAGCGGAGCAGCCGAGCGAGTTAGTGTCAGCCGAGGGCCGAAACCGGAAGGCGGT GCGATGGAACCAGCGGAGCAGCCGAGCGAGTTGGTGTCAGCCGAGGGCCGAAACCGGAAGGCGGT T C RABIF Ensembl:ENSG00000183155 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:202889018..202889130 26863196 MeRIP-seq:(Medium) rs1557980797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074695 Human_Splice_Rec_175463 76365 RMVar_ID_76365 Human_SNP_ID_46428103 m1A Human chr1 + 202943811 202943811 202943811 TAGGAGTGGCAAACCGGTCCCACTGCGCCACAATGATGGCAGAAATGCCCAGGACACAGACGATG TAGGAGTGGCAAACCGGTCCCACTGCGCCACAGTGATGGCAGAAATGCCCAGGACACAGACGATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202943751..202943982 32194978 MeRIP-seq:(Medium) rs369530077 Functional Loss SNV dbSNP153 33..33 33 - - - 76366 RMVar_ID_76366 Human_SNP_ID_46428104 m1A Human chr1 + 202943811 202943811 202943811 TAGGAGTGGCAAACCGGTCCCACTGCGCCACAATGATGGCAGAAATGCCCAGGACACAGACGATG TAGGAGTGGCAAACCGGTCCCACTGCGCCACATTGATGGCAGAAATGCCCAGGACACAGACGATG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202943751..202943982 32194978 MeRIP-seq:(Medium) rs369530077 Functional Loss SNV dbSNP153 33..33 33 - - - 76367 RMVar_ID_76367 Human_SNP_ID_46428768 m1A Human chr1 - 202946592 202946592 202946592 TGTATATGTTCTAGGTCTGGGAGGGACGTTGGAGGGTCATCCCATATGATGTGCTCCCTGACTGG TGTATATGTTCTAGGTCTGGGAGGGACGTTGGCGGGTCATCCCATATGATGTGCTCCCTGACTGG T G ADIPOR1 Ensembl:ENSG00000159346 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:202946485..202946652 26863196 MeRIP-seq:(Medium) rs1474964396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973929,Human_RBP_ID_1733423,Human_RBP_ID_4017637,Human_RBP_ID_5740438,Human_RBP_ID_8961262,Human_RBP_ID_10730123,Human_RBP_ID_17735663,Human_RBP_ID_22486750,Human_RBP_ID_24556110 Human_Splice_Rec_175516,Human_Splice_Rec_175530,Human_Splice_Rec_175544,Human_Splice_Rec_175556 RMVar_hsa_circ_44820,RMVar_hsa_circ_326523,RMVar_hsa_circ_268295,RMVar_hsa_circ_139017,RMVar_hsa_circ_56413 76368 RMVar_ID_76368 Human_SNP_ID_46429200 m1A Human chr1 - 202948347 202948347 202948347 GGAGGAGGTGCGGGTACTGACACTTCCCCTGCAAGCCCACCACGCCATGGAGAAGATGGAAGAGT GGAGGAGGTGCGGGTACTGACACTTCCCCTGCGAGCCCACCACGCCATGGAGAAGATGGAAGAGT T C ADIPOR1 Ensembl:ENSG00000159346 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1186438169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224318,Human_RBP_ID_338101,Human_RBP_ID_746683,Human_RBP_ID_4017645,Human_RBP_ID_17735665,Human_RBP_ID_18966332 Human_Splice_Rec_175514,Human_Splice_Rec_175515,Human_Splice_Rec_175528,Human_Splice_Rec_175529,Human_Splice_Rec_175542,Human_Splice_Rec_175543,Human_Splice_Rec_175554,Human_Splice_Rec_175555 RMVar_hsa_circ_44820,RMVar_hsa_circ_268295,RMVar_hsa_circ_56413,RMVar_hsa_circ_57249,RMVar_hsa_circ_347464 76369 RMVar_ID_76369 Human_SNP_ID_46429204 m1A Human chr1 - 202948358 202948358 202948358 CAGGAAGAAGAGGAGGAGGTGCGGGTACTGACACTTCCCCTGCAAGCCCACCACGCCATGGAGAA CAGGAAGAAGAGGAGGAGGTGCGGGTACTGACGCTTCCCCTGCAAGCCCACCACGCCATGGAGAA T C ADIPOR1 Ensembl:ENSG00000159346 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs943266435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224318,Human_RBP_ID_338102,Human_RBP_ID_746683,Human_RBP_ID_1733427,Human_RBP_ID_4017646,Human_RBP_ID_8295275,Human_RBP_ID_18966332 Human_Splice_Rec_175514,Human_Splice_Rec_175515,Human_Splice_Rec_175528,Human_Splice_Rec_175529,Human_Splice_Rec_175542,Human_Splice_Rec_175543,Human_Splice_Rec_175554,Human_Splice_Rec_175555 RMVar_hsa_circ_44820,RMVar_hsa_circ_268295,RMVar_hsa_circ_56413,RMVar_hsa_circ_57249,RMVar_hsa_circ_347464 76370 RMVar_ID_76370 Human_SNP_ID_46429209 m1A Human chr1 + 202948371 202948371 202948371 GGTGGGCTTGCAGGGGAAGTGTCAGTACCCGCACCTCCTCCTCTTCTTCCTGGGGCACTGGGCAT GGTGGGCTTGCAGGGGAAGTGTCAGTACCCGCCCCTCCTCCTCTTCTTCCTGGGGCACTGGGCAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:202948251..202948468;chr1:202948326..202948425 26863196 MeRIP-seq:(Medium) rs1032425169 Functional Loss SNV dbSNP153 33..33 33 - - - 76371 RMVar_ID_76371 Human_SNP_ID_46431587 m1A Human chr1 - 202958273 202958273 202958273 GCGCCCCTTCCGGCGCGGGGAGGGCGCTGAAGATCGGGGCCGCTCGGCCGCAGGCCGCCTCCAGC GCGCCCCTTCCGGCGCGGGGAGGGCGCTGAAGCTCGGGGCCGCTCGGCCGCAGGCCGCCTCCAGC T G ADIPOR1 Ensembl:ENSG00000159346 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:202958136..202958328 26863196 MeRIP-seq:(Medium) rs928384668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224320,Human_RBP_ID_746686,Human_RBP_ID_4017664,Human_RBP_ID_17735671 Human_Splice_Rec_175511,Human_Splice_Rec_175525,Human_Splice_Rec_175549 76372 RMVar_ID_76372 Human_SNP_ID_46432568 m1A Human chr1 + 202962611 202962611 202962611 TGGCAGGCCAGCTGCACCATTGGGGGTGGCCCACAAAGCAGTACCAGCACATCATCCCCTGGAGC TGGCAGGCCAGCTGCACCATTGGGGGTGGCCCGCAAAGCAGTACCAGCACATCATCCCCTGGAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:202962561..202962710 32194978 MeRIP-seq:(Medium) rs139281039 Functional Loss SNV dbSNP153 33..33 33 - - - 76373 RMVar_ID_76373 Human_SNP_ID_46433801 m1A Human chr1 + 202966885 202966885 202966885 GCAGAGTGACCAGCCCCACCCCCAGGGAGGCCAGCAGGACGGGGCTCTGTGGGTAGAGGAGGCAG GCAGAGTGACCAGCCCCACCCCCAGGGAGGCCGGCAGGACGGGGCTCTGTGGGTAGAGGAGGCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:202966592..202966889 26863196 MeRIP-seq:(Medium) rs1422833463 Functional Loss SNV dbSNP153 33..33 33 - - - 76374 RMVar_ID_76374 Human_SNP_ID_46433912 m1A Human chr1 + 202967204 202967204 202967204 TACTGAATGAGGGTCTTACCGTCTGGATCCCCATGACGGAGCGCCTTTTCCTCCACCACCTGACA TACTGAATGAGGGTCTTACCGTCTGGATCCCCGTGACGGAGCGCCTTTTCCTCCACCACCTGACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:202966592..202967250 26863196 MeRIP-seq:(Medium) rs567416582 Functional Loss SNV dbSNP153 33..33 33 - - - 76375 RMVar_ID_76375 Human_SNP_ID_46443804 m1A Human chr1 - 203007438 203007438 203007438 GCCATGTCTCCGGCCGGAGAGCCGGCCCCGGGAGCCGCAAGCCAGCTCCGCCCGGCTCCGCGGCC GCCATGTCTCCGGCCGGAGAGCCGGCCCCGGGCGCCGCAAGCCAGCTCCGCCCGGCTCCGCGGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:203007376..203007799 26863196 MeRIP-seq:(Medium) rs1379262925 Functional Loss SNV dbSNP153 33..33 33 - - - 76376 RMVar_ID_76376 Human_SNP_ID_46454357 m1A Human chr1 - 203047192 203047192 203047192 GTCCTGGGTCTGCTGGGACACAGCCAGGCTGCAGGTTCCGTCCTCGAAGCAGCTGAGCTGCACAC GTCCTGGGTCTGCTGGGACACAGCCAGGCTGCGGGTTCCGTCCTCGAAGCAGCTGAGCTGCACAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:203039147..203049752 32194978 MeRIP-seq:(Medium) rs114629482 Functional Loss SNV dbSNP153 33..33 33 - - - 76377 RMVar_ID_76377 Human_SNP_ID_46518161 m1A Human chr1 + 203307190 203307190 203307190 GCTGCATTCGCATCAACCACAAGATGGACCCCATCATCAGCAGGGTGGCCAGCCAGATCGGACTC GCTGCATTCGCATCAACCACAAGATGGACCCCCTCATCAGCAGGGTGGCCAGCCAGATCGGACTC A C BTG2 Ensembl:ENSG00000159388 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:203307143..203307213 26863196 MeRIP-seq:(Medium) rs1272895939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_176258,Human_Splice_Rec_176262 Human_miRNA_ID_334408,Human_miRNA_ID_1092289,Human_miRNA_ID_2510548,Human_miRNA_ID_2673968,Human_miRNA_ID_2924724,Human_miRNA_ID_3053370 RMVar_hsa_circ_103046,RMVar_hsa_circ_139032 76378 RMVar_ID_76378 Human_SNP_ID_46570814 m1A Human chr1 + 203515648 203515648 203515648 GTAAGAGCTGAAAATCATTCCACAGAGGTAGGACTCTTTGGCAGAGGGAACAGCTGAATCCAGGG GTAAGAGCTGAAAATCATTCCACAGAGGTAGGGCTCTTTGGCAGAGGGAACAGCTGAATCCAGGG A G lnc-OPTC-2,lnc-OPTC-2:2,lnc-OPTC-2:3 RNACentral:URS0000D5B6AE,RNACentral:URS0000D58DBF,RNACentral:URS0000D5D09F lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:203515610..203515814 26863196 MeRIP-seq:(Medium) rs1348516737 Functional Loss SNV dbSNP153 33..33 33 - - - 76379 RMVar_ID_76379 Human_SNP_ID_46640723 m1A Human chr1 - 203795777 203795777 203795777 AACGGGTCTAGTTACCAGAGAACAGAAACTTTACCGAACCGATGACACTATCCCCGACTCCCGCT AACGGGTCTAGTTACCAGAGAACAGAAACTTTGCCGAACCGATGACACTATCCCCGACTCCCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:203795740..203795837 26863196 MeRIP-seq:(Medium) rs1258989490 Functional Loss SNV dbSNP153 33..33 33 - - - 76380 RMVar_ID_76380 Human_SNP_ID_46640724 m1A Human chr1 - 203795777 203795777 203795777 AACGGGTCTAGTTACCAGAGAACAGAAACTTTACCGAACCGATGACACTATCCCCGACTCCCGCT AACGGGTCTAGTTACCAGAGAACAGAAACTTTCCCGAACCGATGACACTATCCCCGACTCCCGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:203795740..203795837 26863196 MeRIP-seq:(Medium) rs1258989490 Functional Loss SNV dbSNP153 33..33 33 - - - 76381 RMVar_ID_76381 Human_SNP_ID_46640730 m1A Human chr1 - 203795796 203795796 203795796 GCCACCCGGGAATCAAAAAAACGGGTCTAGTTACCAGAGAACAGAAACTTTACCGAACCGATGAC GCCACCCGGGAATCAAAAAAACGGGTCTAGTTCCCAGAGAACAGAAACTTTACCGAACCGATGAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:203795746..203795823;chr1:203795756..203795903 26863196 MeRIP-seq:(Medium) rs1024973567 Functional Loss SNV dbSNP153 33..33 33 - - - 76382 RMVar_ID_76382 Human_SNP_ID_46653746 m1A Human chr1 + 203842411 203842411 203842411 TCGCGGTCAGGAGCTGGAGACCAGCCCGGCCAACACGGCGAAACCCCGTCTCCACCAAAACATGC TCGCGGTCAGGAGCTGGAGACCAGCCCGGCCAGCACGGCGAAACCCCGTCTCCACCAAAACATGC A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:203842398..203842463 26863196 MeRIP-seq:(Medium) rs1423100657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65402,RMVar_hsa_circ_119203,RMVar_hsa_circ_139083,RMVar_hsa_circ_110721,RMVar_hsa_circ_139085,RMVar_hsa_circ_333312,RMVar_hsa_circ_367470,RMVar_hsa_circ_63203 76383 RMVar_ID_76383 Human_SNP_ID_46658594 m1A Human chr1 + 203861667 203861667 203861667 GGTGTGCTCTTTGTGAAATTCCACCATGGCGTACCGTGGCCAGGGTCAGAAAGTGCAGAAGGTTA GGTGTGCTCTTTGTGAAATTCCACCATGGCGTCCCGTGGCCAGGGTCAGAAAGTGCAGAAGGTTA A C SNRPE Ensembl:ENSG00000182004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:203861601..203862012;chr1:203861601..203862225;chr1:203861601..203862143;chr1:203861601..203862045 26863196 MeRIP-seq:(Medium) rs767777578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222965,Human_RBP_ID_338428,Human_RBP_ID_744226,Human_RBP_ID_1419059,Human_RBP_ID_4074711,Human_RBP_ID_5311938,Human_RBP_ID_5741322,Human_RBP_ID_8295443,Human_RBP_ID_8961389,Human_RBP_ID_9319321,Human_RBP_ID_9478987,Human_RBP_ID_18429298,Human_RBP_ID_22133654,Human_RBP_ID_22431227,Human_RBP_ID_23205520,Human_RBP_ID_23356823,Human_RBP_ID_26374188,Human_RBP_ID_26850491,Human_RBP_ID_27173970 Human_Splice_Rec_176835,Human_Splice_Rec_176849,Human_Splice_Rec_176857 Human_miRNA_ID_2673970,Human_miRNA_ID_2924726 RMVar_hsa_circ_96625,RMVar_hsa_circ_139093 76384 RMVar_ID_76384 Human_SNP_ID_46658595 m1A Human chr1 + 203861667 203861667 203861667 GGTGTGCTCTTTGTGAAATTCCACCATGGCGTACCGTGGCCAGGGTCAGAAAGTGCAGAAGGTTA GGTGTGCTCTTTGTGAAATTCCACCATGGCGTTCCGTGGCCAGGGTCAGAAAGTGCAGAAGGTTA A T SNRPE Ensembl:ENSG00000182004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:203861601..203862012;chr1:203861601..203862225;chr1:203861601..203862143;chr1:203861601..203862045 26863196 MeRIP-seq:(Medium) rs767777578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222965,Human_RBP_ID_338428,Human_RBP_ID_744226,Human_RBP_ID_1419059,Human_RBP_ID_4074711,Human_RBP_ID_5311938,Human_RBP_ID_5741322,Human_RBP_ID_8295443,Human_RBP_ID_8961389,Human_RBP_ID_9319321,Human_RBP_ID_9478987,Human_RBP_ID_18429298,Human_RBP_ID_22133654,Human_RBP_ID_22431227,Human_RBP_ID_23205520,Human_RBP_ID_23356823,Human_RBP_ID_26374188,Human_RBP_ID_26850491,Human_RBP_ID_27173970 Human_Splice_Rec_176835,Human_Splice_Rec_176849,Human_Splice_Rec_176857 Human_miRNA_ID_2673970,Human_miRNA_ID_2924726 RMVar_hsa_circ_96625,RMVar_hsa_circ_139093 76385 RMVar_ID_76385 Human_SNP_ID_46658734 m1A Human chr1 - 203862153 203862153 203862153 GTGGCTAAGGAAAAAATACAAAAGCAGCATAGACTCTGCTTCCTGAAACAACCGGACGACGCTAT GTGGCTAAGGAAAAAATACAAAAGCAGCATAGCCTCTGCTTCCTGAAACAACCGGACGACGCTAT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:203862151..203862225 26863410 MeRIP-seq:(Medium) rs1205723643 Functional Loss SNV dbSNP153 33..33 33 - - - 76386 RMVar_ID_76386 Human_SNP_ID_46659116 m1A Human chr1 + 203863595 203863589 203863595 CCTCCCTCGGCCTCCGAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCTATTTTTC CCTCCCTCGGCCTCCGAAAGTGCTGGG______GGCGTGAGCCACCGCGCCCGGCCCTATTTTTC GATTACA G SNRPE Ensembl:ENSG00000182004 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:203863592..203863789 26863410 MeRIP-seq:(Medium) rs1291130593 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_96625,RMVar_hsa_circ_139093 76387 RMVar_ID_76387 Human_SNP_ID_46719306 m1A Human chr1 - 204104957 204104957 204104957 CAAACCTAGCCCCTTTCTGCCCAAAACAAATCACCAGCCACTTCCTCTTCTAACCAGTCAACAAC CAAACCTAGCCCCTTTCTGCCCAAAACAAATCCCCAGCCACTTCCTCTTCTAACCAGTCAACAAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204104954..204105105 26863196 MeRIP-seq:(Medium) rs996052701 Functional Loss SNV dbSNP153 33..33 33 - - - 76388 RMVar_ID_76388 Human_SNP_ID_46731441 m1A Human chr1 - 204151971 204151971 204151971 CGGCGGGCCGCGAGCCGGCGATCGAAGCGGGCAGCTCGCGCCTGAGTCATGGACTTCCCCTGGCC CGGCGGGCCGCGAGCCGGCGATCGAAGCGGGCGGCTCGCGCCTGAGTCATGGACTTCCCCTGGCC T C ETNK2 Ensembl:ENSG00000143845 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:204151921..204152007;chr1:204151921..204152027 26863196 MeRIP-seq:(Medium) rs550740913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4018449 76389 RMVar_ID_76389 Human_SNP_ID_46749389 m1A Human chr1 - 204222013 204222013 204222013 AGAGAGAGAGAGAGAGAGAGAGAGATCCTCAGAGTGGAAGGAGGGGGAAGCAGCAGGACACATTG AGAGAGAGAGAGAGAGAGAGAGAGATCCTCAGGGTGGAAGGAGGGGGAAGCAGCAGGACACATTG T C PLEKHA6 Ensembl:ENSG00000143850 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204221963..204222164 26863196 MeRIP-seq:(Medium) rs999715991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5137738,Human_RBP_ID_5741815 RMVar_hsa_circ_111774,RMVar_hsa_circ_139112 76390 RMVar_ID_76390 Human_SNP_ID_46761583 m1A Human chr1 - 204270345 204270345 204270345 GACAGGTCTTGGCTATAGCTTAGGGAGATTTTATCATATTGCTTATAGCTCAAGCAATGGGTATG GACAGGTCTTGGCTATAGCTTAGGGAGATTTTGTCATATTGCTTATAGCTCAAGCAATGGGTATG T C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204270339..204270404 26863196 MeRIP-seq:(Medium) rs923040448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139122,RMVar_hsa_circ_78050,RMVar_hsa_circ_69473,RMVar_hsa_circ_7354,RMVar_hsa_circ_318691,RMVar_hsa_circ_355402 76391 RMVar_ID_76391 Human_SNP_ID_46762990 m1A Human chr1 - 204276781 204276781 204276781 AATTGGTAGTGCCGGGATAGAATGAGGACGTCATTTGTAGGGGTTGCTGGGTAGGAAAGTCTGGG AATTGGTAGTGCCGGGATAGAATGAGGACGTCTTTTGTAGGGGTTGCTGGGTAGGAAAGTCTGGG T A PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204276777..204276863 26863196 MeRIP-seq:(Medium) rs778188577 Functional Loss SNV dbSNP153 33..33 33 - - - 76392 RMVar_ID_76392 Human_SNP_ID_46781752 m1A Human chr1 - 204358802 204358802 204358802 GCAGGGAAGGGGGCTGTGGAGCCTGGGAGAGCAGAGATGGAGAACCGGGATAGAGGGAGAGCCAT GCAGGGAAGGGGGCTGTGGAGCCTGGGAGAGCGGAGATGGAGAACCGGGATAGAGGGAGAGCCAT T C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204358800..204358931 26863196 MeRIP-seq:(Medium) rs1191020421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18928870 76393 RMVar_ID_76393 Human_SNP_ID_46781774 m1A Human chr1 - 204358885 204358875 204358885 AAAGTGGCGGGGGTGGGGGAGAAGGGAGAAGAAGGGAGAAGAGGCTCCTGGGAAATGCTCTTTGA AAAGTGGCGGGGGTGGGGGAGAAGGGAGAAGA__________GGCTCCTGGGAAATGCTCTTTGA CTCTTCTCCCT C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204358841..204359047 26863196 MeRIP-seq:(Medium) rs1165857474 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_2116331,Human_RBP_ID_8167306,Human_RBP_ID_18928871,Human_RBP_ID_26774676 76394 RMVar_ID_76394 Human_SNP_ID_46781775 m1A Human chr1 - 204358885 204358883 204358886 AAAGTGGCGGGGGTGGGGGAGAAGGGAGAAGAAGGGAGAAGAGGCTCCTGGGAAATGCTCTTTGA AAAGTGGCGGGGGTGGGGGAGAAGGGAGAAG___GGAGAAGAGGCTCCTGGGAAATGCTCTTTGA CCTT C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204358841..204359047 26863196 MeRIP-seq:(Medium) rs1425947176 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2116331,Human_RBP_ID_8167306,Human_RBP_ID_18928871,Human_RBP_ID_26774676 76395 RMVar_ID_76395 Human_SNP_ID_46783771 m1A Human chr1 - 204367475 204367475 204367475 AAAGTAGAGGAACGAGGCTGTTCTAGACACACAGGCAGAGGTTCAGAGGCAGGAGACGCAGCCGC AAAGTAGAGGAACGAGGCTGTTCTAGACACACGGGCAGAGGTTCAGAGGCAGGAGACGCAGCCGC T C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204367440..204367544 26863196 MeRIP-seq:(Medium) rs1255406459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25231 76396 RMVar_ID_76396 Human_SNP_ID_46785442 m1A Human chr1 + 204374717 204374716 204374717 CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCTATAGTCTAAACACGCTGCCTCCCACTCAATGCC CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCT_TAGTCTAAACACGCTGCCTCCCACTCAATGCC TA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204374705..204374817 26863196 MeRIP-seq:(Medium) rs1190692015 Functional Loss DEL dbSNP153 33..33 33 - - - 76397 RMVar_ID_76397 Human_SNP_ID_46785443 m1A Human chr1 + 204374717 204374717 204374717 CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCTATAGTCTAAACACGCTGCCTCCCACTCAATGCC CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCTCTAGTCTAAACACGCTGCCTCCCACTCAATGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204374705..204374817 26863196 MeRIP-seq:(Medium) rs920736792 Functional Loss SNV dbSNP153 33..33 33 - - - 76398 RMVar_ID_76398 Human_SNP_ID_46785444 m1A Human chr1 + 204374717 204374717 204374717 CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCTATAGTCTAAACACGCTGCCTCCCACTCAATGCC CCCTTTATCCTCCTCCTCTGTCTGTGTCTTCTGTAGTCTAAACACGCTGCCTCCCACTCAATGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204374705..204374817 26863196 MeRIP-seq:(Medium) rs920736792 Functional Loss SNV dbSNP153 33..33 33 - - - 76399 RMVar_ID_76399 Human_SNP_ID_46792707 m1A Human chr1 - 204406216 204406216 204406216 GGAAGAATTTGCAAGGGATGGATGCAGGTTCCAGAAACGAATTCAAGAAACAGAAGATGCTATTG GGAAGAATTTGCAAGGGATGGATGCAGGTTCCGGAAACGAATTCAAGAAACAGAAGATGCTATTG T C PPP1R15B Ensembl:ENSG00000158615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:204406165..204406260 26863196 MeRIP-seq:(Medium) rs778049239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25369,Human_RBP_ID_338574,Human_RBP_ID_974066,Human_RBP_ID_1419196,Human_RBP_ID_1733665,Human_RBP_ID_5742158,Human_RBP_ID_8741113,Human_RBP_ID_10735533,Human_RBP_ID_17763068,Human_RBP_ID_22017893,Human_RBP_ID_23357294 Human_Splice_Rec_177344 76400 RMVar_ID_76400 Human_SNP_ID_46793892 m1A Human chr1 + 204410525 204410525 204410525 CCTGTTGAAGGAATTCCAGCCGTTTCATGCGAAGATGGTGAATTTCTGGTAGGCCTTCCGTAGAA CCTGTTGAAGGAATTCCAGCCGTTTCATGCGACGATGGTGAATTTCTGGTAGGCCTTCCGTAGAA A C AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:204410048..204410547 32194978 MeRIP-seq:(Medium) rs760847763 Functional Loss SNV dbSNP153 33..33 33 - - - 76401 RMVar_ID_76401 Human_SNP_ID_46793961 m1A Human chr1 + 204410700 204410700 204410700 GACTACCTCGCTATTTCCATCACTGTTCTGATAGCTGACTTCTAGCCTAGGAAAGCAGTCCAGGT GACTACCTCGCTATTTCCATCACTGTTCTGATGGCTGACTTCTAGCCTAGGAAAGCAGTCCAGGT A G AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:204410651..204410870 26863196 MeRIP-seq:(Medium) rs1332845006 Functional Loss SNV dbSNP153 33..33 33 - - - 76402 RMVar_ID_76402 Human_SNP_ID_46794180 m1A Human chr1 - 204411176 204411176 204411176 CCAGCTCCTTGCGCCGCTCCCCGGATTGCTTCAGAAGGTGCTAATTTGGAGCCAACTTTTCGGTG CCAGCTCCTTGCGCCGCTCCCCGGATTGCTTCTGAAGGTGCTAATTTGGAGCCAACTTTTCGGTG T A PPP1R15B Ensembl:ENSG00000158615 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:204411126..204411225 26863196 MeRIP-seq:(Medium) rs778000547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338587,Human_RBP_ID_4018643,Human_RBP_ID_8741173,Human_RBP_ID_17448809,Human_RBP_ID_19152555,Human_RBP_ID_22024132,Human_RBP_ID_27174065 Human_miRNA_ID_738054,Human_miRNA_ID_742067,Human_miRNA_ID_746071 76403 RMVar_ID_76403 Human_SNP_ID_46794197 m1A Human chr1 + 204411210 204411210 204411210 AAGCAATCCGGGGAGCGGCGCAAGGAGCTGGGAGAGCAGTTTCGTCCAGTAACTGACCCGAGTCT AAGCAATCCGGGGAGCGGCGCAAGGAGCTGGGGGAGCAGTTTCGTCCAGTAACTGACCCGAGTCT A G AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:204411099..204411800 26863196 MeRIP-seq:(Medium) rs1027202698 Functional Loss SNV dbSNP153 33..33 33 - - - 76404 RMVar_ID_76404 Human_SNP_ID_46794207 m1A Human chr1 - 204411227 204411227 204411227 TTCCTCTGCCCAGCCCGAGACTCGGGTCAGTTACTGGACGAAACTGCTCTCCCAGCTCCTTGCGC TTCCTCTGCCCAGCCCGAGACTCGGGTCAGTTGCTGGACGAAACTGCTCTCCCAGCTCCTTGCGC T C PPP1R15B Ensembl:ENSG00000158615 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:204411176..204411394;chr1:204411176..204411250 26863196 MeRIP-seq:(Medium) rs751708347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272229,Human_RBP_ID_338588,Human_RBP_ID_1419257,Human_RBP_ID_4087449,Human_RBP_ID_8295599,Human_RBP_ID_8741175,Human_RBP_ID_10735742,Human_RBP_ID_17338614,Human_RBP_ID_22024133,Human_RBP_ID_23357312,Human_RBP_ID_27174066,Human_RBP_ID_27392867,Human_RBP_ID_27584954 76405 RMVar_ID_76405 Human_SNP_ID_46794238 m1A Human chr1 - 204411284 204411284 204411284 CTCTTCTAAGTTCCCGACGCCTCTTGGCCCGGAAAACTCCGGGAACCCCACACTGCTTTCCTCTG CTCTTCTAAGTTCCCGACGCCTCTTGGCCCGGTAAACTCCGGGAACCCCACACTGCTTTCCTCTG T A PPP1R15B Ensembl:ENSG00000158615 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204411237..204411401 26863196 MeRIP-seq:(Medium) rs761893411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25377,Human_RBP_ID_17214931,Human_RBP_ID_17339228,Human_RBP_ID_22026118,Human_RBP_ID_27392867 76406 RMVar_ID_76406 Human_SNP_ID_46794371 m1A Human chr1 + 204411616 204411616 204411616 GCGGCAGAACACAGGGAAGAACAGCCCGCGCAATAGGCGGCGACTGATGCGACTTCCATCCTGGC GCGGCAGAACACAGGGAAGAACAGCCCGCGCAGTAGGCGGCGACTGATGCGACTTCCATCCTGGC A G AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204411565..204411748 26863196 MeRIP-seq:(Medium) rs191595952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5538232,Human_RBP_ID_8053061 76407 RMVar_ID_76407 Human_SNP_ID_46794453 m1A Human chr1 - 204411799 204411799 204411799 CGGGCCCTGCGGCCATTTTGGGCTTCGCTTCCACCGCACCAGCCGGCCTACCCAGTCCTTCCGGT CGGGCCCTGCGGCCATTTTGGGCTTCGCTTCCGCCGCACCAGCCGGCCTACCCAGTCCTTCCGGT T C PPP1R15B Ensembl:ENSG00000158615 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204411751..204411800 26863196 MeRIP-seq:(Medium) rs1190944710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4087470,Human_RBP_ID_5485234 76408 RMVar_ID_76408 Human_SNP_ID_46805118 m1A Human chr1 - 204454703 204454703 204454703 GCCCCCTGCAGACCCGAAGAGCTCACTTCTCCAAGTACCTCTTCCACCTCATCGTCTGGGACCAG GCCCCCTGCAGACCCGAAGAGCTCACTTCTCCTAGTACCTCTTCCACCTCATCGTCTGGGACCAG T A PIK3C2B Ensembl:ENSG00000133056 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:204454676..204454864 26863196 MeRIP-seq:(Medium) rs1039984786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_177368,Human_Splice_Rec_177369,Human_Splice_Rec_177434,Human_Splice_Rec_177435,Human_Splice_Rec_177484 Human_miRNA_ID_2614288 RMVar_hsa_circ_88342,RMVar_hsa_circ_101510,RMVar_hsa_circ_139131,RMVar_hsa_circ_61272,RMVar_hsa_circ_139134,RMVar_hsa_circ_265937,RMVar_hsa_circ_9781,RMVar_hsa_circ_44793,RMVar_hsa_circ_37088,RMVar_hsa_circ_328652,RMVar_hsa_circ_19419 76409 RMVar_ID_76409 Human_SNP_ID_46809255 m1A Human chr1 - 204469374 204469368 204469374 GGTTCAGATGGGGGAGTCTCTTCGTCCCCAGGACCAGGGGACATAGAGGGCTCTTGCAAGAAACT GGTTCAGATGGGGGAGTCTCTTCGTCCCCAGG______GGACATAGAGGGCTCTTGCAAGAAACT CCCTGGT C PIK3C2B Ensembl:ENSG00000133056 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204469323..204469409 26863196 MeRIP-seq:(Medium) rs768572772 Functional Loss DEL dbSNP153 33..38 33 - - - Human_miRNA_ID_2038509,Human_miRNA_ID_2038510,Human_miRNA_ID_2435913,Human_miRNA_ID_2435914,Human_miRNA_ID_3017491,Human_miRNA_ID_3017492 RMVar_hsa_circ_23990,RMVar_hsa_circ_88342,RMVar_hsa_circ_139134,RMVar_hsa_circ_90606,RMVar_hsa_circ_139144,RMVar_hsa_circ_139146,RMVar_hsa_circ_139145,RMVar_hsa_circ_374415,RMVar_hsa_circ_285041 76410 RMVar_ID_76410 Human_SNP_ID_46809257 m1A Human chr1 - 204469374 204469374 204469374 GGTTCAGATGGGGGAGTCTCTTCGTCCCCAGGACCAGGGGACATAGAGGGCTCTTGCAAGAAACT GGTTCAGATGGGGGAGTCTCTTCGTCCCCAGGGCCAGGGGACATAGAGGGCTCTTGCAAGAAACT T C PIK3C2B Ensembl:ENSG00000133056 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204469323..204469409 26863196 MeRIP-seq:(Medium) rs770338375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2038509,Human_miRNA_ID_2038510,Human_miRNA_ID_2435913,Human_miRNA_ID_2435914,Human_miRNA_ID_3017491,Human_miRNA_ID_3017492 RMVar_hsa_circ_23990,RMVar_hsa_circ_88342,RMVar_hsa_circ_139134,RMVar_hsa_circ_90606,RMVar_hsa_circ_139144,RMVar_hsa_circ_139146,RMVar_hsa_circ_139145,RMVar_hsa_circ_374415,RMVar_hsa_circ_285041 76411 RMVar_ID_76411 Human_SNP_ID_46811319 m1A Human chr1 + 204478282 204478282 204478282 CTCACCCATACCCCCAATCCCACCTCCTTTGCAGCCAGGGACCCTGCCTCGCATCTCACTCCACA CTCACCCATACCCCCAATCCCACCTCCTTTGCCGCCAGGGACCCTGCCTCGCATCTCACTCCACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204478279..204478406 26863196 MeRIP-seq:(Medium) rs969767439 Functional Loss SNV dbSNP153 33..33 33 - - - 76412 RMVar_ID_76412 Human_SNP_ID_46815264 m1A Human chr1 - 204494647 204494644 204494648 GCTGCCGCTATTGTCTCACCCGGGGTGGCCTGACTCTGCGAGCTCGCGCACGCTCTCGGCGGAGA GCTGCCGCTATTGTCTCACCCGGGGTGGCCT____CTGCGAGCTCGCGCACGCTCTCGGCGGAGA GAGTC G PIK3C2B Ensembl:ENSG00000133056 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:204494601..204494763 26863196 MeRIP-seq:(Medium) rs1357363067 Functional Loss DEL dbSNP153 32..35 33 - - - 76413 RMVar_ID_76413 Human_SNP_ID_46818390 m1A Human chr1 + 204506583 204506583 204506583 CATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA CATCAGACTTTTAATCTGAGGGTCCAGGGTTCCAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA A C TRK1,TRK-TTT3-1,lnc-MDM4-11,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS0000D5A196,RNACentral:URS000022DD4A tRNA,tRNA,lincRNA,tRNA intron,exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs774381440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338605,Human_RBP_ID_1151435,Human_RBP_ID_1419274,Human_RBP_ID_1733694,Human_RBP_ID_3293101,Human_RBP_ID_5273323,Human_RBP_ID_5456902,Human_RBP_ID_5742266,Human_RBP_ID_8240448,Human_RBP_ID_8295625,Human_RBP_ID_10736042,Human_RBP_ID_17341578,Human_RBP_ID_17676204,Human_RBP_ID_17736019,Human_RBP_ID_18508809,Human_RBP_ID_18522871,Human_RBP_ID_18560471,Human_RBP_ID_19256498,Human_RBP_ID_22781817,Human_RBP_ID_23122008,Human_RBP_ID_23357364,Human_RBP_ID_24396206,Human_RBP_ID_26850610,Human_RBP_ID_27153539 76414 RMVar_ID_76414 Human_SNP_ID_46818391 m1A Human chr1 + 204506583 204506583 204506583 CATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA CATCAGACTTTTAATCTGAGGGTCCAGGGTTCGAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA A G TRK1,TRK-TTT3-1,lnc-MDM4-11,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS0000D5A196,RNACentral:URS000022DD4A tRNA,tRNA,lincRNA,tRNA intron,exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs774381440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338605,Human_RBP_ID_1151435,Human_RBP_ID_1419274,Human_RBP_ID_1733694,Human_RBP_ID_3293101,Human_RBP_ID_5273323,Human_RBP_ID_5456902,Human_RBP_ID_5742266,Human_RBP_ID_8240448,Human_RBP_ID_8295625,Human_RBP_ID_10736042,Human_RBP_ID_17341578,Human_RBP_ID_17676204,Human_RBP_ID_17736019,Human_RBP_ID_18508809,Human_RBP_ID_18522871,Human_RBP_ID_18560471,Human_RBP_ID_19256498,Human_RBP_ID_22781817,Human_RBP_ID_23122008,Human_RBP_ID_23357364,Human_RBP_ID_24396206,Human_RBP_ID_26850610,Human_RBP_ID_27153539 76415 RMVar_ID_76415 Human_SNP_ID_46818392 m1A Human chr1 + 204506583 204506583 204506583 CATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA CATCAGACTTTTAATCTGAGGGTCCAGGGTTCTAGTCCCTGTTCGGGCGTTTGTAGTTTTCGTTA A T TRK1,TRK-TTT3-1,lnc-MDM4-11,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS0000D5A196,RNACentral:URS000022DD4A tRNA,tRNA,lincRNA,tRNA intron,exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs774381440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338605,Human_RBP_ID_1151435,Human_RBP_ID_1419274,Human_RBP_ID_1733694,Human_RBP_ID_3293101,Human_RBP_ID_5273323,Human_RBP_ID_5456902,Human_RBP_ID_5742266,Human_RBP_ID_8240448,Human_RBP_ID_8295625,Human_RBP_ID_10736042,Human_RBP_ID_17341578,Human_RBP_ID_17676204,Human_RBP_ID_17736019,Human_RBP_ID_18508809,Human_RBP_ID_18522871,Human_RBP_ID_18560471,Human_RBP_ID_19256498,Human_RBP_ID_22781817,Human_RBP_ID_23122008,Human_RBP_ID_23357364,Human_RBP_ID_24396206,Human_RBP_ID_26850610,Human_RBP_ID_27153539 76416 RMVar_ID_76416 Human_SNP_ID_46818459 m1A Human chr1 - 204506624 204506623 204506624 TCCGCTCTTGGGACTTGATGGGATAATTTAGCAGGTTAAAGTAACGAAAACTACAAACGCCCGAA TCCGCTCTTGGGACTTGATGGGATAATTTAGC_GGTTAAAGTAACGAAAACTACAAACGCCCGAA CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204506592..204506667 26863196 MeRIP-seq:(Medium) rs772908476 Functional Loss DEL dbSNP153 33..33 33 - - - 76417 RMVar_ID_76417 Human_SNP_ID_46818460 m1A Human chr1 - 204506624 204506624 204506624 TCCGCTCTTGGGACTTGATGGGATAATTTAGCAGGTTAAAGTAACGAAAACTACAAACGCCCGAA TCCGCTCTTGGGACTTGATGGGATAATTTAGCTGGTTAAAGTAACGAAAACTACAAACGCCCGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204506592..204506667 26863196 MeRIP-seq:(Medium) rs919419413 Functional Loss SNV dbSNP153 33..33 33 - - - 76418 RMVar_ID_76418 Human_SNP_ID_46818461 m1A Human chr1 - 204506624 204506624 204506624 TCCGCTCTTGGGACTTGATGGGATAATTTAGCAGGTTAAAGTAACGAAAACTACAAACGCCCGAA TCCGCTCTTGGGACTTGATGGGATAATTTAGCGGGTTAAAGTAACGAAAACTACAAACGCCCGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204506592..204506667 26863196 MeRIP-seq:(Medium) rs919419413 Functional Loss SNV dbSNP153 33..33 33 - - - 76419 RMVar_ID_76419 Human_SNP_ID_46818743 m1A Human chr1 - 204507045 204507045 204507045 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGTCTTGTTCTCTTTTCCT ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAGGTCCCTGTTCGGGCGTCTTGTTCTCTTTTCCT T C TRK1,TRK-TTT3-1,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS000022DD4A tRNA,tRNA,tRNA intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1054581648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1151440,Human_RBP_ID_1252275,Human_RBP_ID_1419276,Human_RBP_ID_1733699,Human_RBP_ID_3293104,Human_RBP_ID_5253160,Human_RBP_ID_5273326,Human_RBP_ID_5742271,Human_RBP_ID_8240450,Human_RBP_ID_8295628,Human_RBP_ID_8741202,Human_RBP_ID_10736047,Human_RBP_ID_18508811,Human_RBP_ID_18560474,Human_RBP_ID_22786867,Human_RBP_ID_23122015,Human_RBP_ID_23303112,Human_RBP_ID_23357368,Human_RBP_ID_24396211,Human_RBP_ID_24449507 76420 RMVar_ID_76420 Human_SNP_ID_46818744 m1A Human chr1 - 204507045 204507045 204507045 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGTCTTGTTCTCTTTTCCT ATCAGACTTTTAATCTGAGGGTCCAGGGTTCACGTCCCTGTTCGGGCGTCTTGTTCTCTTTTCCT T G TRK1,TRK-TTT3-1,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS000022DD4A tRNA,tRNA,tRNA intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1054581648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1151440,Human_RBP_ID_1252275,Human_RBP_ID_1419276,Human_RBP_ID_1733699,Human_RBP_ID_3293104,Human_RBP_ID_5253160,Human_RBP_ID_5273326,Human_RBP_ID_5742271,Human_RBP_ID_8240450,Human_RBP_ID_8295628,Human_RBP_ID_8741202,Human_RBP_ID_10736047,Human_RBP_ID_18508811,Human_RBP_ID_18560474,Human_RBP_ID_22786867,Human_RBP_ID_23122015,Human_RBP_ID_23303112,Human_RBP_ID_23357368,Human_RBP_ID_24396211,Human_RBP_ID_24449507 76421 RMVar_ID_76421 Human_SNP_ID_46821311 m1A Human chr1 + 204516494 204516494 204516494 CCCCCCACCCGGGCTCGGCGGGGGAGCGACTCATGGAGCTGCCGTAAGGTGTGGCTCTTGGCCTT CCCCCCACCCGGGCTCGGCGGGGGAGCGACTCGTGGAGCTGCCGTAAGGTGTGGCTCTTGGCCTT A G MDM4 Ensembl:ENSG00000198625 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204516445..204516903 26863196 MeRIP-seq:(Medium) rs1288238040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223130,Human_RBP_ID_338607,Human_RBP_ID_801955,Human_RBP_ID_18429308,Human_RBP_ID_22871026 Human_Splice_Rec_177495,Human_Splice_Rec_177509,Human_Splice_Rec_177521,Human_Splice_Rec_177539,Human_Splice_Rec_177547,Human_Splice_Rec_177551,Human_Splice_Rec_177569,Human_Splice_Rec_177577,Human_Splice_Rec_177597,Human_Splice_Rec_177617,Human_Splice_Rec_177637,Human_Splice_Rec_177653 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815 76422 RMVar_ID_76422 Human_SNP_ID_46847151 m1A Human chr1 + 204618983 204618983 204618983 TGAGAGCGTTGTTGTTGAGCATGAGGGTCTCCATCTGGGGCAGGTGGTGGAAGGCGCGGGGGTGG TGAGAGCGTTGTTGTTGAGCATGAGGGTCTCCGTCTGGGGCAGGTGGTGGAAGGCGCGGGGGTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:204618938..204619065 26863196 MeRIP-seq:(Medium) rs758863160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76688,RMVar_hsa_circ_87144,RMVar_hsa_circ_139162,RMVar_hsa_circ_139170 76423 RMVar_ID_76423 Human_SNP_ID_46848934 m1A Human chr1 - 204626147 204626147 204626147 GTGGGAGGAGATGTTGCATTTAGGACAAGCAGAATGGGAGGAGCCTCTGAGACTGCCGAGTAGAG GTGGGAGGAGATGTTGCATTTAGGACAAGCAGGATGGGAGGAGCCTCTGAGACTGCCGAGTAGAG T C LRRN2 Ensembl:ENSG00000170382 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204626118..204626245 26863196 MeRIP-seq:(Medium) rs1242955001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139171 76424 RMVar_ID_76424 Human_SNP_ID_46856799 m1A Human chr1 + 204660148 204660148 204660148 CTGGTCCAGGGGGTGACAGCAGGCCAAGCTCCATACCCTTGGCTTGTTCACAGGACTCCTGCTCC CTGGTCCAGGGGGTGACAGCAGGCCAAGCTCCGTACCCTTGGCTTGTTCACAGGACTCCTGCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:204660111..204660390 26863196 MeRIP-seq:(Medium) rs1011425453 Functional Loss SNV dbSNP153 33..33 33 - - - 76425 RMVar_ID_76425 Human_SNP_ID_46857645 m1A Human chr1 + 204664269 204664269 204664269 ACTATTATGCATTCATGATTCCAGCTTCAACCAGTCCTCTCTGCTGCAATCCCTTTATTCCTCCT ACTATTATGCATTCATGATTCCAGCTTCAACCGGTCCTCTCTGCTGCAATCCCTTTATTCCTCCT A G AL161793.1 Ensembl:ENSG00000228153 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:204664266..204664599 26863196 MeRIP-seq:(Medium) rs2772234 Functional Loss SNV dbSNP153 33..33 33 - - - 76426 RMVar_ID_76426 Human_SNP_ID_46959107 m1A Human chr1 - 205087348 205087348 205087348 CTATTAAAAGACAAAAATTAGCTGGGCGTGGTAGTACATGCCTGTAATCCCAGCTACACTGGAGG CTATTAAAAGACAAAAATTAGCTGGGCGTGGTTGTACATGCCTGTAATCCCAGCTACACTGGAGG T A RBBP5 Ensembl:ENSG00000117222 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12409915 Functional Loss SNV dbSNP153 33..33 33 - - - 76427 RMVar_ID_76427 Human_SNP_ID_46959108 m1A Human chr1 - 205087348 205087348 205087348 CTATTAAAAGACAAAAATTAGCTGGGCGTGGTAGTACATGCCTGTAATCCCAGCTACACTGGAGG CTATTAAAAGACAAAAATTAGCTGGGCGTGGTGGTACATGCCTGTAATCCCAGCTACACTGGAGG T C RBBP5 Ensembl:ENSG00000117222 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12409915 Functional Loss SNV dbSNP153 33..33 33 - - - 76428 RMVar_ID_76428 Human_SNP_ID_46967191 m1A Human chr1 - 205120077 205120077 205120077 GATTGCATATAGTGCTGATGAGTAAGAGAGTGACGTGAAAAATGGTGAGAGCAAATAATGATGCT GATTGCATATAGTGCTGATGAGTAAGAGAGTGGCGTGAAAAATGGTGAGAGCAAATAATGATGCT T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:205119921..205120277 26863196 MeRIP-seq:(Medium) rs990525163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10739110,Human_RBP_ID_23357891 76429 RMVar_ID_76429 Human_SNP_ID_46967624 m1A Human chr1 + 205121910 205121904 205121911 GCGGACTGTGGCCGCCCGGTCTCAGCTCCGGCAACAACACCTTCTCCCCGGCCGGCTTCAGCAAC GCGGACTGTGGCCGCCCGGTCTCAGCT_______CAACACCTTCTCCCCGGCCGGCTTCAGCAAC TCCGGCAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:205121857..205121934;chr1:205121800..205121925 26863196 MeRIP-seq:(Medium) rs777528973 Functional Loss DEL dbSNP153 28..34 33 - - - 76430 RMVar_ID_76430 Human_SNP_ID_46967626 m1A Human chr1 + 205121910 205121908 205121911 GCGGACTGTGGCCGCCCGGTCTCAGCTCCGGCAACAACACCTTCTCCCCGGCCGGCTTCAGCAAC GCGGACTGTGGCCGCCCGGTCTCAGCTCCGG___CAACACCTTCTCCCCGGCCGGCTTCAGCAAC GCAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:205121857..205121934;chr1:205121800..205121925 26863196 MeRIP-seq:(Medium) rs748972565 Functional Loss DEL dbSNP153 32..34 33 - - - 76431 RMVar_ID_76431 Human_SNP_ID_46972800 m1A Human chr1 + 205144020 205144020 205144020 CGCTTGCTCAGTCAATGAGCTACTCTTTGCAGAGGATCAGGGAACTAAGGTATGCCTGGGGAAAC CGCTTGCTCAGTCAATGAGCTACTCTTTGCAGGGGATCAGGGAACTAAGGTATGCCTGGGGAAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:205143915..205144035 32194978 MeRIP-seq:(Medium) rs1163954785 Functional Loss SNV dbSNP153 33..33 33 - - - 76432 RMVar_ID_76432 Human_SNP_ID_46983148 m1A Human chr1 + 205187603 205187603 205187603 GAGCGCCAGGCTGACCCGAGTCTGAGTCCCATAGGTGAAGCGGAGGCGCCGAAGCTTACAGCTCT GAGCGCCAGGCTGACCCGAGTCTGAGTCCCATGGGTGAAGCGGAGGCGCCGAAGCTTACAGCTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205187552..205187703 26863196 MeRIP-seq:(Medium) rs1282285757 Functional Loss SNV dbSNP153 33..33 33 - - - 76433 RMVar_ID_76433 Human_SNP_ID_46989112 m1A Human chr1 + 205211656 205211656 205211656 GAATCCGCCTCCTGACGCCCCCGCCTGCAGTCAGCCTGGCTCCCAACCTCCGTCACTGCCGTTGC GAATCCGCCTCCTGACGCCCCCGCCTGCAGTCGGCCTGGCTCCCAACCTCCGTCACTGCCGTTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:205211388..205211688 26863196 MeRIP-seq:(Medium) rs1370240198 Functional Loss SNV dbSNP153 33..33 33 - - - 76434 RMVar_ID_76434 Human_SNP_ID_47015845 m1A Human chr1 + 205321639 205321638 205321639 GCGCGAAAACCAGCGACTCCATGGCGAGCAGGAGGTGAGCAAGGGCGGCAGGGGAATCAGTAGGC GCGCGAAAACCAGCGACTCCATGGCGAGCAGG_GGTGAGCAAGGGCGGCAGGGGAATCAGTAGGC GA G HSALNG0009935 RNACentral:URS0000EBEF98 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:205321590..205321711 26863196 MeRIP-seq:(Medium) rs1558677946 Functional Loss DEL dbSNP153 33..33 33 - - - 76435 RMVar_ID_76435 Human_SNP_ID_47060587 m1A Human chr1 - 205505650 205505650 205505650 CAGGGAATCCCCGCCCCCCACAGGGCGAAAACAGAGGCCTCCAGTCCAGACCCGATTTTGGATTT CAGGGAATCCCCGCCCCCCACAGGGCGAAAACTGAGGCCTCCAGTCCAGACCCGATTTTGGATTT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:205505608..205505740 26863196 MeRIP-seq:(Medium) rs1277713120 Functional Loss SNV dbSNP153 33..33 33 - - - 76436 RMVar_ID_76436 Human_SNP_ID_47062122 m1A Human chr1 - 205512191 205512191 205512191 TGACCTCATCCCCTCCCGAAGTGGAAACCACCACCCGCGTGCTGATGACTCCAGATCTGTAGCCC TGACCTCATCCCCTCCCGAAGTGGAAACCACCGCCCGCGTGCTGATGACTCCAGATCTGTAGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:205512186..205512759 26863196 MeRIP-seq:(Medium) rs940005742 Functional Loss SNV dbSNP153 33..33 33 - - - 76437 RMVar_ID_76437 Human_SNP_ID_47093100 m1A Human chr1 + 205631674 205631674 205631674 CGCGGGGCTCCCCCTCGGTCTCCGCCTCGAACACGATGCGCCTCTCCGCCCTCAGCCTCCTCCTC CGCGGGGCTCCCCCTCGGTCTCCGCCTCGAACGCGATGCGCCTCTCCGCCCTCAGCCTCCTCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:205631574..205631964 26863196 MeRIP-seq:(Medium) rs1484917580 Functional Loss SNV dbSNP153 33..33 33 - - - 76438 RMVar_ID_76438 Human_SNP_ID_47105015 m1A Human chr1 - 205679812 205679812 205679812 TGCTCAGGCCCAGGCCGGCTTTCTTGAGGAAGAGTGAGTTATTAAGACAGGGAAAGGGGACTGAG TGCTCAGGCCCAGGCCGGCTTTCTTGAGGAAGGGTGAGTTATTAAGACAGGGAAAGGGGACTGAG T C SLC45A3 Ensembl:ENSG00000158715 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:205679802..205679894 26863196 MeRIP-seq:(Medium) rs1355631270 Functional Loss SNV dbSNP153 33..33 33 - - - 76439 RMVar_ID_76439 Human_SNP_ID_47113402 m1A Human chr1 + 205715652 205715651 205715652 CTAGAATGTAGTGTCAGTCAGCATAGCTGCTGAAATCTACGTTGTAGAGGTAAACCTAGCAGAGC CTAGAATGTAGTGTCAGTCAGCATAGCTGCTG_AATCTACGTTGTAGAGGTAAACCTAGCAGAGC GA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:205715601..205715750 32194978 MeRIP-seq:(Medium) rs1307154253 Functional Loss DEL dbSNP153 33..33 33 - - - 76440 RMVar_ID_76440 Human_SNP_ID_47113717 m1A Human chr1 + 205717022 205717022 205717022 CTAGTCAAGGACAGGATGGGAAGTAAGTGAAGAATAGGGCCAGGAAAATAGTGTCCTATAGCAGA CTAGTCAAGGACAGGATGGGAAGTAAGTGAAGGATAGGGCCAGGAAAATAGTGTCCTATAGCAGA A G lnc-MFSD4A-1,lnc-MFSD4A-1:2 RNACentral:URS00009BFD13,RNACentral:URS00008BD54D lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205716971..205717166 26863196 MeRIP-seq:(Medium) rs1011112971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139226,RMVar_hsa_circ_139225 76441 RMVar_ID_76441 Human_SNP_ID_47114118 m1A Human chr1 + 205718402 205718399 205718402 GCTTTCCGGTTCCTCATCTTCTTCTTTGGGAGAAGGAGTCTTTTCCTTTGATGCCTTTGAAGCTG GCTTTCCGGTTCCTCATCTTCTTCTTTGGG___AGGAGTCTTTTCCTTTGATGCCTTTGAAGCTG GAGA G lnc-MFSD4A-1,lnc-MFSD4A-1:2 RNACentral:URS00009BFD13,RNACentral:URS00008BD54D lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:205718351..205718500 32194978 MeRIP-seq:(Medium) rs747731454 Functional Loss DEL dbSNP153 31..33 33 - - - 76442 RMVar_ID_76442 Human_SNP_ID_47114404 m1A Human chr1 + 205719671 205719671 205719671 ATCTTCCATTAGGAAATCTTCATCGCTGCCGGAATCTTCTGAGAAGAAAGAAGAATTTCAACATC ATCTTCCATTAGGAAATCTTCATCGCTGCCGGCATCTTCTGAGAAGAAAGAAGAATTTCAACATC A C lnc-MFSD4A-1,lnc-MFSD4A-1:2 RNACentral:URS00009BFD13,RNACentral:URS00008BD54D lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205719487..205719708 26863196 MeRIP-seq:(Medium) rs1412747519 Functional Loss SNV dbSNP153 33..33 33 - - - 76443 RMVar_ID_76443 Human_SNP_ID_47116173 m1A Human chr1 + 205727777 205727777 205727777 TCTCGGGGAGATGATCGAATTTTCTTAGTGGGAGGGCCCGAATCTCTTCCATAATCTTCATCTAA TCTCGGGGAGATGATCGAATTTTCTTAGTGGGTGGGCCCGAATCTCTTCCATAATCTTCATCTAA A T lnc-MFSD4A-1,lnc-MFSD4A-1:2 RNACentral:URS00009BFD13,RNACentral:URS00008BD54D lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:205727726..205727800 32194978 MeRIP-seq:(Medium) rs1284569184 Functional Loss SNV dbSNP153 33..33 33 - - - 76444 RMVar_ID_76444 Human_SNP_ID_47122231 m1A Human chr1 + 205750094 205750094 205750094 TCAGCCGATGGGACCGCTGCTGCCGAACCCCGAGCTGCTGGCTTCTCAAACTCCGCTGCTCTTTG TCAGCCGATGGGACCGCTGCTGCCGAACCCCGGGCTGCTGGCTTCTCAAACTCCGCTGCTCTTTG A G lnc-MFSD4A-1,lnc-MFSD4A-1:2 RNACentral:URS00009BFD13,RNACentral:URS00008BD54D lincRNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:205750051..205750200 26863196 MeRIP-seq:(Medium) rs565954129 Functional Loss SNV dbSNP153 33..33 33 - - - 76445 RMVar_ID_76445 Human_SNP_ID_47122235 m1A Human chr1 - 205750118 205750118 205750118 TCGTCTGTTCCAGGAGCCCTGAACCAAAGAGCAGCGGAGTTTGAGAAGCCAGCAGCTCGGGGTTC TCGTCTGTTCCAGGAGCCCTGAACCAAAGAGCCGCGGAGTTTGAGAAGCCAGCAGCTCGGGGTTC T G NUCKS1 Ensembl:ENSG00000069275 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr1:205750101..205750125;chr1:205750072..205750185 26863196,32194978 MeRIP-seq:(Medium) rs1381856558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24207,Human_RBP_ID_339205,Human_RBP_ID_1151562,Human_RBP_ID_1419621,Human_RBP_ID_1734130,Human_RBP_ID_3293582,Human_RBP_ID_4074717,Human_RBP_ID_5744564,Human_RBP_ID_8296082,Human_RBP_ID_8741707,Human_RBP_ID_9357444,Human_RBP_ID_10742286,Human_RBP_ID_18415136,Human_RBP_ID_18560853,Human_RBP_ID_23122055,Human_RBP_ID_23358577,Human_RBP_ID_24541554,Human_RBP_ID_24626343,Human_RBP_ID_26312594,Human_RBP_ID_26851011,Human_RBP_ID_27799172 76446 RMVar_ID_76446 Human_SNP_ID_47122238 m1A Human chr1 - 205750124 205750122 205750124 GGGGGCTCGTCTGTTCCAGGAGCCCTGAACCAAAGAGCAGCGGAGTTTGAGAAGCCAGCAGCTCG GGGGGCTCGTCTGTTCCAGGAGCCCTGAACCA__GAGCAGCGGAGTTTGAGAAGCCAGCAGCTCG CTT C NUCKS1 Ensembl:ENSG00000069275 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr1:205749902..205750200;chr1:205749932..205750164 26863196,26863410 MeRIP-seq:(Medium) rs1328574223 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24207,Human_RBP_ID_223568,Human_RBP_ID_339205,Human_RBP_ID_1151562,Human_RBP_ID_1419621,Human_RBP_ID_1734130,Human_RBP_ID_3293582,Human_RBP_ID_4074717,Human_RBP_ID_5485271,Human_RBP_ID_5744564,Human_RBP_ID_8296082,Human_RBP_ID_9357444,Human_RBP_ID_10742286,Human_RBP_ID_18415136,Human_RBP_ID_18560853,Human_RBP_ID_23122055,Human_RBP_ID_24541554,Human_RBP_ID_24626343,Human_RBP_ID_26312594,Human_RBP_ID_26851011,Human_RBP_ID_27393118,Human_RBP_ID_27799172 76447 RMVar_ID_76447 Human_SNP_ID_47128083 m1A Human chr1 - 205774940 205774940 205774940 GCACACCCCGCTAGCCATGGGCAGCCGCGACCACCTGTTCAAAGTGCTGGTGGTGGGGGACGCCG GCACACCCCGCTAGCCATGGGCAGCCGCGACCGCCTGTTCAAAGTGCTGGTGGTGGGGGACGCCG T C RAB29 Ensembl:ENSG00000117280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205774889..205774987 26863196 MeRIP-seq:(Medium) rs1199020175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339250,Human_RBP_ID_4019616,Human_RBP_ID_8741711 76448 RMVar_ID_76448 Human_SNP_ID_47133462 m1A Human chr1 - 205796997 205796997 205796997 GTCATTTTGTCTTTATGTCTCTATAGTGTGGGAGGCCTCATCTTGGACAAGACTGTCTCAGACCC GTCATTTTGTCTTTATGTCTCTATAGTGTGGGGGGCCTCATCTTGGACAAGACTGTCTCAGACCC T C SLC41A1 Ensembl:ENSG00000133065 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:205796947..205798812 32194978 MeRIP-seq:(Medium) rs1411281708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_179980,Human_Splice_Rec_179981,Human_Splice_Rec_180000,Human_Splice_Rec_180001 RMVar_hsa_circ_11049,RMVar_hsa_circ_80783,RMVar_hsa_circ_91136,RMVar_hsa_circ_139234,RMVar_hsa_circ_139235 76449 RMVar_ID_76449 Human_SNP_ID_47136790 m1A Human chr1 - 205810912 205810912 205810912 GAAGCTGACAGAGCCCAGCCAAAGGAGCGGGAAGGAGCCGCAGCCCCAGGCTGGCACTGTGTTCT GAAGCTGACAGAGCCCAGCCAAAGGAGCGGGAGGGAGCCGCAGCCCCAGGCTGGCACTGTGTTCT T C SLC41A1 Ensembl:ENSG00000133065 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:205810863..205813081 32194978 MeRIP-seq:(Medium) rs911074766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108516,RMVar_hsa_circ_139241 76450 RMVar_ID_76450 Human_SNP_ID_47136809 m1A Human chr1 - 205811013 205811013 205811013 GAAGAGGTATTAGCTCTTCCCAGGAAGGGAGGAAGTTTCTGGAAGAGAAGGGAAAGACGGCAGAC GAAGAGGTATTAGCTCTTCCCAGGAAGGGAGGCAGTTTCTGGAAGAGAAGGGAAAGACGGCAGAC T G SLC41A1 Ensembl:ENSG00000133065 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:205810963..205812982 32194978 MeRIP-seq:(Medium) rs1017835552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_179988,Human_Splice_Rec_180012 Human_miRNA_ID_3115777 RMVar_hsa_circ_108516,RMVar_hsa_circ_139241 76451 RMVar_ID_76451 Human_SNP_ID_47230096 m1A Human chr1 - 206203560 206203560 206203560 TCCCCTCTCTTCCCCGCCACCCGTTTCTACGCAGATCGGTGCCCCAGTCCCTGGAGGAGCCTCCG TCCCCTCTCTTCCCCGCCACCCGTTTCTACGCTGATCGGTGCCCCAGTCCCTGGAGGAGCCTCCG T A FAM72A Ensembl:ENSG00000196550 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:206203536..206203614 26863196 MeRIP-seq:(Medium) rs1313170416 Functional Loss SNV dbSNP153 33..33 33 - - - 76452 RMVar_ID_76452 Human_SNP_ID_47254259 m1A Human chr1 - 206333454 206333454 206333454 CAGAGACCTTCGCCTCGCCCCGCCGGTTCCTCACCCTCGGGGAGCAACATGGATAATCTCAGTGA CAGAGACCTTCGCCTCGCCCCGCCGGTTCCTCGCCCTCGGGGAGCAACATGGATAATCTCAGTGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:206333432..206333525 26863410 MeRIP-seq:(Medium) rs2747583 Functional Loss SNV dbSNP153 33..33 33 - - - 76453 RMVar_ID_76453 Human_SNP_ID_47269783 m1A Human chr1 + 206406577 206406577 206406577 CAGCAAGAGACAGAGCAGTTTTATTTCACAGTAAGGGAGTGCTATGGCTTTTAAAGAGCGTCAGC CAGCAAGAGACAGAGCAGTTTTATTTCACAGTGAGGGAGTGCTATGGCTTTTAAAGAGCGTCAGC A G SRGAP2 Ensembl:ENSG00000266028 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2772061 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_17825,RMVar_hsa_circ_20663,RMVar_hsa_circ_278499,RMVar_hsa_circ_311480,RMVar_hsa_circ_330047,RMVar_hsa_circ_340937,RMVar_hsa_circ_1893,RMVar_hsa_circ_291672,RMVar_hsa_circ_276542,RMVar_hsa_circ_2271,RMVar_hsa_circ_349015,RMVar_hsa_circ_60834,RMVar_hsa_circ_69076 76454 RMVar_ID_76454 Human_SNP_ID_47294797 m1A Human chr1 - 206507604 206507604 206507604 GGCGCTGCCCGATGGCCGGGGACGCCATGGCCATGCCCGGCTAGTGGCGGCAGCTTTGGCAGCGG GGCGCTGCCCGATGGCCGGGGACGCCATGGCCGTGCCCGGCTAGTGGCGGCAGCTTTGGCAGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:206507557..206507879 26863196 MeRIP-seq:(Medium) rs1553393893 Functional Loss SNV dbSNP153 33..33 33 - - - 76455 RMVar_ID_76455 Human_SNP_ID_47319346 m1A Human chr1 + 206612381 206612381 206612381 TGGGGTGGCCTGGGGAAGAGAGCACAGAAGCCAGGGAATGTCAAGAAAGCGAGGGCGCAGCAGCT TGGGGTGGCCTGGGGAAGAGAGCACAGAAGCCTGGGAATGTCAAGAAAGCGAGGGCGCAGCAGCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:206612333..206612435 26863196 MeRIP-seq:(Medium) rs781955199 Functional Loss SNV dbSNP153 33..33 33 - - - 76456 RMVar_ID_76456 Human_SNP_ID_47319364 m1A Human chr1 + 206612425 206612425 206612425 GAAAGCGAGGGCGCAGCAGCTGCCAGGCCCTCAGCCGTGGGGGCAGCCATGCTGGGGCCCGGCCG GAAAGCGAGGGCGCAGCAGCTGCCAGGCCCTCGGCCGTGGGGGCAGCCATGCTGGGGCCCGGCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:206612307..206612469 26863196 MeRIP-seq:(Medium) rs924573790 Functional Loss SNV dbSNP153 33..33 33 - - - 76457 RMVar_ID_76457 Human_SNP_ID_47337049 m1A Human chr1 + 206685075 206685075 206685075 GCGGCGCGCGGTGGGACCCACGGAGCCCCGCGACCCGCCGAGCCTGGAGCCGGGCCGGGTCGGGG GCGGCGCGCGGTGGGACCCACGGAGCCCCGCGCCCCGCCGAGCCTGGAGCCGGGCCGGGTCGGGG A C MAPKAPK2 Ensembl:ENSG00000162889 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:206685014..206685300 26863196 MeRIP-seq:(Medium) rs1553425250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073248,Human_RBP_ID_18475476,Human_RBP_ID_27801462 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76458 RMVar_ID_76458 Human_SNP_ID_47337136 m1A Human chr1 + 206685294 206685288 206685295 GGTGCCGTTCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGG GGTGCCGTTCCCCGCCCCGGCCCCGCC_______CCCCCCACCCCTGCCCTGCCGCACCCCCCGG CGCCGCAG C MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:206685193..206685293 26863410 MeRIP-seq:(Medium) rs1553425336 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76459 RMVar_ID_76459 Human_SNP_ID_47337140 m1A Human chr1 + 206685294 206685294 206685294 GGTGCCGTTCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGG GGTGCCGTTCCCCGCCCCGGCCCCGCCGCCGCCGCCCCCCACCCCTGCCCTGCCGCACCCCCCGG A C MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:206685193..206685293 26863410 MeRIP-seq:(Medium) rs1425759842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76460 RMVar_ID_76460 Human_SNP_ID_47337141 m1A Human chr1 + 206685294 206685294 206685294 GGTGCCGTTCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGG GGTGCCGTTCCCCGCCCCGGCCCCGCCGCCGCTGCCCCCCACCCCTGCCCTGCCGCACCCCCCGG A T MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:206685193..206685293 26863410 MeRIP-seq:(Medium) rs1425759842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76461 RMVar_ID_76461 Human_SNP_ID_47337149 m1A Human chr1 + 206685302 206685302 206685302 TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCCCCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG A C MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:206684876..206685493 26863410 MeRIP-seq:(Medium) rs181345810 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22532177 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76462 RMVar_ID_76462 Human_SNP_ID_47337150 m1A Human chr1 + 206685302 206685302 206685302 TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCGCCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG A G MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:206684876..206685493 26863410 MeRIP-seq:(Medium) rs181345810 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22532177 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76463 RMVar_ID_76463 Human_SNP_ID_47337153 m1A Human chr1 - 206685307 206685307 206685307 GGCGGCGGCTGCGCCGGGGGGTGCGGCAGGGCAGGGGTGGGGGGCTGCGGCGGCGGGGCCGGGGC GGCGGCGGCTGCGCCGGGGGGTGCGGCAGGGCGGGGGTGGGGGGCTGCGGCGGCGGGGCCGGGGC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:206684993..206685343 26863410 MeRIP-seq:(Medium) rs1361343319 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 76464 RMVar_ID_76464 Human_SNP_ID_47337223 m1A Human chr1 + 206685453 206685453 206685453 GGTCACCAGCCAGGTCCTGGGGCTGGGCATCAACGGCAAAGTTTTGCAGATCTTCAACAAGAGGA GGTCACCAGCCAGGTCCTGGGGCTGGGCATCAGCGGCAAAGTTTTGCAGATCTTCAACAAGAGGA A G MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:206684926..206685500 26863196 MeRIP-seq:(Medium) rs1331532151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9359817,Human_RBP_ID_17736641,Human_RBP_ID_18969558,Human_RBP_ID_27801463 Human_Splice_Rec_181165,Human_Splice_Rec_181183 Human_miRNA_ID_2031245,Human_miRNA_ID_2886184 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 76465 RMVar_ID_76465 Human_SNP_ID_47339748 m1A Human chr1 - 206696095 206696095 206696095 CTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAAGGTGAAGGCAGGTGAGATGAATCCT CTGGCAAAGAAATCATCTGCCGTGTGACTGGTGGGATGAAGGTGAAGGCAGGTGAGATGAATCCT T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879954703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1839027 76466 RMVar_ID_76466 Human_SNP_ID_47339757 m1A Human chr1 - 206696120 206696120 206696120 ACTTTTGTCCATGTCACTGATCTTTCTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAA ACTTTTGTCCATGTCACTGATCTTTCTGGCAAGGAAATCATCTGCCGTGTGACTGGTAGGATGAA T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:206696101..206696175 32194978 MeRIP-seq:(Medium) rs782188132 Functional Loss SNV dbSNP153 33..33 33 - - - 76467 RMVar_ID_76467 Human_SNP_ID_47340453 m1A Human chr1 - 206699265 206699265 206699265 CCTTTATTGGCCACCCTGGTGCCCAGACACTTACCCCCACCCACTCCCTGAAACTCTTCCTTCAG CCTTTATTGGCCACCCTGGTGCCCAGACACTTTCCCCCACCCACTCCCTGAAACTCTTCCTTCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:206699260..206699486 26863196 MeRIP-seq:(Medium) rs1190995534 Functional Loss SNV dbSNP153 33..33 33 - - - 76468 RMVar_ID_76468 Human_SNP_ID_47347390 m1A Human chr1 - 206729009 206729009 206729009 GTCCAAACTGAAATGAAGCCACAGTGAGATCCAGAGAACACAACAGCCCGCCGCCACTCTCCACT GTCCAAACTGAAATGAAGCCACAGTGAGATCCGGAGAACACAACAGCCCGCCGCCACTCTCCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:206729005..206729139 26863196 MeRIP-seq:(Medium) rs111694578 Functional Loss SNV dbSNP153 33..33 33 - - - 76469 RMVar_ID_76469 Human_SNP_ID_47348217 m1A Human chr1 + 206731845 206731845 206731845 CTCGGACCCCTTTTCTCTCTTCTCAGCAATCAACAAAGGTCCCTCAAACCCCACTGCACACCAGC CTCGGACCCCTTTTCTCTCTTCTCAGCAATCAGCAAAGGTCCCTCAAACCCCACTGCACACCAGC A G MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:206731836..206731953 26863196 MeRIP-seq:(Medium) rs782340351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22684,Human_RBP_ID_855767,Human_RBP_ID_18966371,Human_RBP_ID_26799404 Human_Splice_Rec_181180,Human_Splice_Rec_181181,Human_Splice_Rec_181198,Human_Splice_Rec_181199,Human_Splice_Rec_181204 Human_miRNA_ID_2351145,Human_miRNA_ID_3046692 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257,RMVar_hsa_circ_38006,RMVar_hsa_circ_109162,RMVar_hsa_circ_139260,RMVar_hsa_circ_108125,RMVar_hsa_circ_93455,RMVar_hsa_circ_101159,RMVar_hsa_circ_139262,RMVar_hsa_circ_103066,RMVar_hsa_circ_269231,RMVar_hsa_circ_139263,RMVar_hsa_circ_139264,RMVar_hsa_circ_105146,RMVar_hsa_circ_139266,RMVar_hsa_circ_100706,RMVar_hsa_circ_139267,RMVar_hsa_circ_139268 76470 RMVar_ID_76470 Human_SNP_ID_47392001 m1A Human chr1 + 206909815 206909815 206909815 GCGCGGTCGCGGCGACCCGCGGGGCCTCTGGGAGCTCTCCAGGGCGCGCATCCTCACGGCCAGTC GCGCGGTCGCGGCGACCCGCGGGGCCTCTGGGTGCTCTCCAGGGCGCGCATCCTCACGGCCAGTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:206909721..206909917 26863196 MeRIP-seq:(Medium) rs1306588532 Functional Loss SNV dbSNP153 33..33 33 - - - 76471 RMVar_ID_76471 Human_SNP_ID_47425897 m1A Human chr1 - 207044014 207044014 207044014 TTTGCCTATTTGCCAGCATTTTTTGAAGTAATACACTGCTGCTACCTGGAAGATGTCTAACTTCA TTTGCCTATTTGCCAGCATTTTTTGAAGTAATTCACTGCTGCTACCTGGAAGATGTCTAACTTCA T A YOD1 Ensembl:ENSG00000180667 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339451,Human_RBP_ID_5745232,Human_RBP_ID_23358982 Human_miRNA_ID_1740664,Human_miRNA_ID_2097677,Human_miRNA_ID_2103620,Human_miRNA_ID_2109575,Human_miRNA_ID_2162123,Human_miRNA_ID_2593329,Human_miRNA_ID_2649035,Human_miRNA_ID_2650981,Human_miRNA_ID_2736291,Human_miRNA_ID_3036890 GWAS_ID_9207,GWAS_ID_9208,GWAS_ID_9209,GWAS_ID_9210,GWAS_ID_9211 RMVar_hsa_circ_76858,RMVar_hsa_circ_98794,RMVar_hsa_circ_119330,RMVar_hsa_circ_82638,RMVar_hsa_circ_139272,RMVar_hsa_circ_139273,RMVar_hsa_circ_139274,RMVar_hsa_circ_139271 76472 RMVar_ID_76472 Human_SNP_ID_47425898 m1A Human chr1 - 207044014 207044014 207044014 TTTGCCTATTTGCCAGCATTTTTTGAAGTAATACACTGCTGCTACCTGGAAGATGTCTAACTTCA TTTGCCTATTTGCCAGCATTTTTTGAAGTAATGCACTGCTGCTACCTGGAAGATGTCTAACTTCA T C YOD1 Ensembl:ENSG00000180667 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339451,Human_RBP_ID_5745232,Human_RBP_ID_23358982 Human_miRNA_ID_1740664,Human_miRNA_ID_2097677,Human_miRNA_ID_2103620,Human_miRNA_ID_2109575,Human_miRNA_ID_2162123,Human_miRNA_ID_2593329,Human_miRNA_ID_2649035,Human_miRNA_ID_2650981,Human_miRNA_ID_2736291,Human_miRNA_ID_3036890 GWAS_ID_9207,GWAS_ID_9208,GWAS_ID_9209,GWAS_ID_9210,GWAS_ID_9211 RMVar_hsa_circ_76858,RMVar_hsa_circ_98794,RMVar_hsa_circ_119330,RMVar_hsa_circ_82638,RMVar_hsa_circ_139272,RMVar_hsa_circ_139273,RMVar_hsa_circ_139274,RMVar_hsa_circ_139271 76473 RMVar_ID_76473 Human_SNP_ID_47428273 m1A Human chr1 + 207053321 207053321 207053321 GCTGTCGGCTCGGTTCGGTCGCGTTACAGGGCAGGCGCCGGGGCCAAGGCAGGGAGGGATCTTAG GCTGTCGGCTCGGTTCGGTCGCGTTACAGGGCGGGCGCCGGGGCCAAGGCAGGGAGGGATCTTAG A G PFKFB2 Ensembl:ENSG00000123836 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:207053271..207053509 26863196 MeRIP-seq:(Medium) rs906856479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074727 Human_Splice_Rec_181635,Human_Splice_Rec_181645,Human_Splice_Rec_181673,Human_Splice_Rec_181675 RMVar_hsa_circ_124011,RMVar_hsa_circ_87355,RMVar_hsa_circ_139275,RMVar_hsa_circ_139276 76474 RMVar_ID_76474 Human_SNP_ID_47437009 m1A Human chr1 + 207089530 207089530 207089530 AATTCCAGCCTGGGGAGAGGACTTTGATCACCAGATGTTTTTTTGGTGTGCGTGCTGTCTTATGG AATTCCAGCCTGGGGAGAGGACTTTGATCACCGGATGTTTTTTTGGTGTGCGTGCTGTCTTATGG A G C4BPB Ensembl:ENSG00000123843 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:207089429..207089550 26863196 MeRIP-seq:(Medium) rs1417798208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10744765,Human_RBP_ID_22429954 Human_Splice_Rec_181722,Human_Splice_Rec_181723,Human_Splice_Rec_181734,Human_Splice_Rec_181735,Human_Splice_Rec_181740,Human_Splice_Rec_181741,Human_Splice_Rec_181749,Human_Splice_Rec_181759,Human_Splice_Rec_181770,Human_Splice_Rec_181771 76475 RMVar_ID_76475 Human_SNP_ID_47437184 m1A Human chr1 - 207090163 207090163 207090163 TGCTCTTCCCAAGTACTCTGTATTCTACTCCCAAGTAGCCGGGACTACAGGCACCCGCCACCACG TGCTCTTCCCAAGTACTCTGTATTCTACTCCCCAGTAGCCGGGACTACAGGCACCCGCCACCACG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:207090162..207090296 26863196 MeRIP-seq:(Medium) rs1337407573 Functional Loss SNV dbSNP153 33..33 33 - - - 76476 RMVar_ID_76476 Human_SNP_ID_47437193 m1A Human chr1 + 207090197 207090197 207090197 GGAGTAGAATACAGAGTACTTGGGAAGAGCACAGGAATCAGGATCAATAATCCAGCAAAAAGACA GGAGTAGAATACAGAGTACTTGGGAAGAGCACGGGAATCAGGATCAATAATCCAGCAAAAAGACA A G C4BPB Ensembl:ENSG00000123843 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:207090184..207090278 26863196 MeRIP-seq:(Medium) rs780834751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24689,Human_RBP_ID_2117577 76477 RMVar_ID_76477 Human_SNP_ID_47489607 m1A Human chr1 - 207321827 207321824 207321827 CGGCCGGCAGGCACAACAGCACCAGCAGCAGCAGCCGGGGCAGCTCCCCGAGGAGGGGCAGCGCC CGGCCGGCAGGCACAACAGCACCAGCAGCAGC___CGGGGCAGCTCCCCGAGGAGGGGCAGCGCC GGCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:207321776..207321875 32194978 MeRIP-seq:(Medium) rs777769984 Functional Loss DEL dbSNP153 33..35 33 - - - 76478 RMVar_ID_76478 Human_SNP_ID_47489793 m1A Human chr1 - 207322387 207322386 207322388 CTGGGCATTAGGTACATCTGGGGGAAGGCCACAGTCACCTAGGGAGACAAAAGCAGAACTGAAGG CTGGGCATTAGGTACATCTGGGGGAAGGCCA__GTCACCTAGGGAGACAAAAGCAGAACTGAAGG CTG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:207322376..207322400 26863196 MeRIP-seq:(Medium) rs867810442 Functional Loss DEL dbSNP153 32..33 33 - - - 76479 RMVar_ID_76479 Human_SNP_ID_47489794 m1A Human chr1 - 207322387 207322387 207322387 CTGGGCATTAGGTACATCTGGGGGAAGGCCACAGTCACCTAGGGAGACAAAAGCAGAACTGAAGG CTGGGCATTAGGTACATCTGGGGGAAGGCCACGGTCACCTAGGGAGACAAAAGCAGAACTGAAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:207322376..207322400 26863196 MeRIP-seq:(Medium) rs1261776205 Functional Loss SNV dbSNP153 33..33 33 - - - 76480 RMVar_ID_76480 Human_SNP_ID_47489865 m1A Human chr1 - 207322566 207322566 207322566 CAGAACTTTTCTAAAAAGATGAAGAACTTACGATTGCAGAACTCTTCAATATCTGACCATTGACT CAGAACTTTTCTAAAAAGATGAAGAACTTACGTTTGCAGAACTCTTCAATATCTGACCATTGACT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:207322516..207324607 32194978 MeRIP-seq:(Medium) rs913635154 Functional Loss SNV dbSNP153 33..33 33 - - - 76481 RMVar_ID_76481 Human_SNP_ID_47490691 m1A Human chr1 - 207325702 207325702 207325702 TGCCCAAACTTACCCTGTGTTACATGAGAAGGAGATGGTTGCACCAAATAATATGCCACCTGGTA TGCCCAAACTTACCCTGTGTTACATGAGAAGGTGATGGTTGCACCAAATAATATGCCACCTGGTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:207325610..207325758 26863196 MeRIP-seq:(Medium) rs1276589725 Functional Loss SNV dbSNP153 33..33 33 - - - 76482 RMVar_ID_76482 Human_SNP_ID_47493116 m1A Human chr1 + 207336742 207336742 207336742 AAGGTCCCACCAACAGTTCAGAAACCTACCACAGTAAATGTTCCAACTACAGAAGTCTCACCAAC AAGGTCCCACCAACAGTTCAGAAACCTACCACCGTAAATGTTCCAACTACAGAAGTCTCACCAAC A C CD55 Ensembl:ENSG00000196352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:207336666..207337073 26863196 MeRIP-seq:(Medium) rs747723739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23489,Human_RBP_ID_10745180,Human_RBP_ID_17221959,Human_RBP_ID_17338632,Human_RBP_ID_22374594,Human_RBP_ID_22752196,Human_RBP_ID_24626940,Human_RBP_ID_26374906 Human_Splice_Rec_181866,Human_Splice_Rec_181867,Human_Splice_Rec_181882,Human_Splice_Rec_181883,Human_Splice_Rec_181900,Human_Splice_Rec_181901,Human_Splice_Rec_181920,Human_Splice_Rec_181921,Human_Splice_Rec_181938,Human_Splice_Rec_181939,Human_Splice_Rec_181958,Human_Splice_Rec_181974,Human_Splice_Rec_181975,Human_Splice_Rec_181996,Human_Splice_Rec_182004,Human_Splice_Rec_182005,Human_Splice_Rec_182014,Human_Splice_Rec_182028,Human_Splice_Rec_182038,Human_Splice_Rec_182039,Human_Splice_Rec_182048,Human_Splice_Rec_182049,Human_Splice_Rec_182057 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 76483 RMVar_ID_76483 Human_SNP_ID_47493155 m1A Human chr1 - 207336820 207336820 207336820 GTGTGTTTTTGAAGAACTGATGGAGTCTCTGTACCTTGAGCATTTGGTGTGGTGGTTTTTGTGGT GTGTGTTTTTGAAGAACTGATGGAGTCTCTGTTCCTTGAGCATTTGGTGTGGTGGTTTTTGTGGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:207336801..207337155 26863196 MeRIP-seq:(Medium) rs879015997 Functional Loss SNV dbSNP153 33..33 33 - - - 76484 RMVar_ID_76484 Human_SNP_ID_47495256 m1A Human chr1 - 207346041 207346041 207346041 CCATTTCTGGCACCCAAGTGAGCCACCTGGAGACCCAATAACTGGCCTGATTGGGCTTGCTAACA CCATTTCTGGCACCCAAGTGAGCCACCTGGAGGCCCAATAACTGGCCTGATTGGGCTTGCTAACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:207346036..207346197 26863196 MeRIP-seq:(Medium) rs953369187 Functional Loss SNV dbSNP153 33..33 33 - - - 76485 RMVar_ID_76485 Human_SNP_ID_47498542 m1A Human chr1 + 207360142 207360142 207360142 TTCGGGTTGGCAAAATATTTTAAAGGTAAAACATGCTGGTGAACCAGGGGTGTTGATGGTGATAA TTCGGGTTGGCAAAATATTTTAAAGGTAAAACGTGCTGGTGAACCAGGGGTGTTGATGGTGATAA A G CD55 Ensembl:ENSG00000196352 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:207359992..207360142 32194978 MeRIP-seq:(Medium) rs55993635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23544,Human_RBP_ID_339575,Human_RBP_ID_2118483,Human_RBP_ID_4020277,Human_RBP_ID_8296421,Human_RBP_ID_17580712,Human_RBP_ID_17676294,Human_RBP_ID_22374609,Human_RBP_ID_23359197,Human_RBP_ID_24627139,Human_RBP_ID_26374938 Human_miRNA_ID_968817,Human_miRNA_ID_2435922,Human_miRNA_ID_2440253 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 76486 RMVar_ID_76486 Human_SNP_ID_47498543 m1A Human chr1 + 207360142 207360142 207360142 TTCGGGTTGGCAAAATATTTTAAAGGTAAAACATGCTGGTGAACCAGGGGTGTTGATGGTGATAA TTCGGGTTGGCAAAATATTTTAAAGGTAAAACTTGCTGGTGAACCAGGGGTGTTGATGGTGATAA A T CD55 Ensembl:ENSG00000196352 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:207359992..207360142 32194978 MeRIP-seq:(Medium) rs55993635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23544,Human_RBP_ID_339575,Human_RBP_ID_2118483,Human_RBP_ID_4020277,Human_RBP_ID_8296421,Human_RBP_ID_17580712,Human_RBP_ID_17676294,Human_RBP_ID_22374609,Human_RBP_ID_23359197,Human_RBP_ID_24627139,Human_RBP_ID_26374938 Human_miRNA_ID_968817,Human_miRNA_ID_2435922,Human_miRNA_ID_2440253 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 76487 RMVar_ID_76487 Human_SNP_ID_47613855 m1A Human chr1 + 207867829 207867805 207867830 CTGGGCCATGGCAGCCTCTGCCCATCCGGCCTAAGGCAGCCTAGCTGCCTTTCCTGCAGGGGAGC CTGGGCCAT_________________________GGCAGCCTAGCTGCCTTTCCTGCAGGGGAGC TGGCAGCCTCTGCCCATCCGGCCTAA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:207867778..207867892 32194978 MeRIP-seq:(Medium) rs1308835284 Functional Loss DEL dbSNP153 10..34 33 - - - 76488 RMVar_ID_76488 Human_SNP_ID_47614281 m1A Human chr1 + 207869121 207869121 207869121 GCCAAGCGCCCCGCTGCAGGCCCGAGATGCGCAGCCGCTGCGGACGCCGGCTCCGCGGCGGCCGC GCCAAGCGCCCCGCTGCAGGCCCGAGATGCGCGGCCGCTGCGGACGCCGGCTCCGCGGCGGCCGC A G lnc-CD46-7,lnc-CD46-7:2,lnc-CD46-7:3,lnc-CD46-7:4 RNACentral:URS0000D5CF1F,RNACentral:URS0000D5A134,RNACentral:URS0000D5BAE3,RNACentral:URS0000D580E7 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:207868885..207869169 26863196 MeRIP-seq:(Medium) rs1306318231 Functional Loss SNV dbSNP153 33..33 33 - - - 76489 RMVar_ID_76489 Human_SNP_ID_47614294 m1A Human chr1 - 207869140 207869138 207869141 GAGCTCACACGCCCGGGAAGCGGCCGCCGCGGAGCCGGCGTCCGCAGCGGCTGCGCATCTCGGGC GAGCTCACACGCCCGGGAAGCGGCCGCCGCG___CCGGCGTCCGCAGCGGCTGCGCATCTCGGGC GCTC G MIR29B2CHG Ensembl:ENSG00000203709 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:207868953..207869157 26863196 MeRIP-seq:(Medium) rs1026032085 Functional Loss DEL dbSNP153 32..34 33 - - - 76490 RMVar_ID_76490 Human_SNP_ID_47687435 m1A Human chr1 - 208176857 208176857 208176857 AGAGGATCCCAGGACTCAAGGAGGAAGGGAGTAGGGCAAAAAGGGAAAGCAGCTGACAGGCAGGC AGAGGATCCCAGGACTCAAGGAGGAAGGGAGTGGGGCAAAAAGGGAAAGCAGCTGACAGGCAGGC T C PLXNA2 Ensembl:ENSG00000076356 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:208176854..208176994 26863196 MeRIP-seq:(Medium) rs1377089300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15394,RMVar_hsa_circ_319729,RMVar_hsa_circ_281809,RMVar_hsa_circ_45883,RMVar_hsa_circ_139331,RMVar_hsa_circ_302767,RMVar_hsa_circ_271611 76491 RMVar_ID_76491 Human_SNP_ID_47838805 m1A Human chr1 + 208799331 208799329 208799331 CACCCCTACTACTGTAACCACTCTGTCACTGTAACCCTTGCCCCTGTGAGCCTGTTCTTCTGCTG CACCCCTACTACTGTAACCACTCTGTCACTG__ACCCTTGCCCCTGTGAGCCTGTTCTTCTGCTG GTA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:208799287..208799416 26863196 MeRIP-seq:(Medium) rs1213499237 Functional Loss DEL dbSNP153 32..33 33 - - - 76492 RMVar_ID_76492 Human_SNP_ID_47947168 m1A Human chr1 + 209245690 209245690 209245690 TGGCTGAAGCTGGAAAATAGCATAATGGTTGAATAGACTGAAAAGGAGCACAATACGGAATCCAG TGGCTGAAGCTGGAAAATAGCATAATGGTTGACTAGACTGAAAAGGAGCACAATACGGAATCCAG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:209245684..209245816 26863196 MeRIP-seq:(Medium) rs1190675642 Functional Loss SNV dbSNP153 33..33 33 - - - 76493 RMVar_ID_76493 Human_SNP_ID_48042090 m1A Human chr1 - 209635900 209635900 209635900 GGAATGAGCTTGGTTTAGGGCTTGAAGAGAAGAGGTGGCCTGAGAGGAGGCAGGGCCCAGGGAGC GGAATGAGCTTGGTTTAGGGCTTGAAGAGAAGGGGTGGCCTGAGAGGAGGCAGGGCCCAGGGAGC T C LAMB3 Ensembl:ENSG00000196878 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:209635887..209636020 26863196 MeRIP-seq:(Medium) rs978483673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81466,RMVar_hsa_circ_139338,RMVar_hsa_circ_126720,RMVar_hsa_circ_79782,RMVar_hsa_circ_139340,RMVar_hsa_circ_113914,RMVar_hsa_circ_139341,RMVar_hsa_circ_106746,RMVar_hsa_circ_139342,RMVar_hsa_circ_139343 76494 RMVar_ID_76494 Human_SNP_ID_48055360 m1A Human chr1 - 209692685 209692683 209692685 CAGGCTCCTGAACCTTCTAGGCCCATCTGGGCACTTCCTTGTAAAATCCAGTTTTACAAAGAATC CAGGCTCCTGAACCTTCTAGGCCCATCTGGGC__TTCCTTGTAAAATCCAGTTTTACAAAGAATC AGT A HSD11B1-AS1 Ensembl:ENSG00000227591 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:209692604..209692686 26863410 MeRIP-seq:(Medium) rs1412395111 Functional Loss DEL dbSNP153 33..34 33 - - - 76495 RMVar_ID_76495 Human_SNP_ID_48086880 m1A Human chr1 + 209828072 209828072 209828072 GTGGGCAAACTTGACGTTTTCGCTATGGGCAAACGCGGGAGCCGGAGCCAGAGCCAGCTACTCAA GTGGGCAAACTTGACGTTTTCGCTATGGGCAATCGCGGGAGCCGGAGCCAGAGCCAGCTACTCAA A T UTP25 Ensembl:ENSG00000117597 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:209828024..209828118 26863196 MeRIP-seq:(Medium) rs1558050138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4020880,Human_RBP_ID_18415137 Human_Splice_Rec_184159 76496 RMVar_ID_76496 Human_SNP_ID_48087685 m1A Human chr1 - 209830958 209830958 209830958 CTACCACCATCTTCATCGTTCATTTCTGCATCATCTACAATACTGTCTTCTTCCTCTTCCTCCTC CTACCACCATCTTCATCGTTCATTTCTGCATCCTCTACAATACTGTCTTCTTCCTCTTCCTCCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:209830909..209830993 26863196 MeRIP-seq:(Medium) rs1380930859 Functional Loss SNV dbSNP153 33..33 33 - - - 76497 RMVar_ID_76497 Human_SNP_ID_48087687 m1A Human chr1 - 209830961 209830961 209830961 TCGCTACCACCATCTTCATCGTTCATTTCTGCATCATCTACAATACTGTCTTCTTCCTCTTCCTC TCGCTACCACCATCTTCATCGTTCATTTCTGCGTCATCTACAATACTGTCTTCTTCCTCTTCCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:209830912..209831085 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76498 RMVar_ID_76498 Human_SNP_ID_170024653 m1A Human chr4 + 10163 10163 10163 TAACCCTAACCCTAACCCTAACCCTAACCCTAACGCTAACCCTAACCCTAACCCTAACCCTAACC TAACCCTAACCCTAACCCTAACCCTAACCCTAGCGCTAACCCTAACCCTAACCCTAACCCTAACC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:10098..10182 26863410 MeRIP-seq:(Medium) rs1301704051 Functional Loss SNV dbSNP153 33..33 33 - - - 76499 RMVar_ID_76499 Human_SNP_ID_170122580 m1A Human chr4 - 342912 342912 342912 GAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCTGAAGCTTTTGGACTTCGGCAGTCTGTT GAGATAATTGAAGTAGATCCTGACACTAAGGAGATGCTGAAGCTTTTGGACTTCGGCAGTCTGTT T C AC079140.2 Ensembl:ENSG00000250321 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1161473317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18033048 76500 RMVar_ID_76500 Human_SNP_ID_170122587 m1A Human chr4 - 342939 342939 342939 AAAAATAAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT AAAAATAAGGTCTCAGCCTTGGATCAGGAGATTATTGAAGTAGATCCTGACACTAAGGAAATGCT T A AC079140.2 Ensembl:ENSG00000250321 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879960082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18408892 76501 RMVar_ID_76501 Human_SNP_ID_170159636 m1A Human chr4 - 474090 474090 474090 GTTAGGGCCTCACTTCCCTGCTTCCACACCTCAGGGAGGCCTCGGTGATTTTGCCAGAGCCTCAG GTTAGGGCCTCACTTCCCTGCTTCCACACCTCGGGGAGGCCTCGGTGATTTTGCCAGAGCCTCAG T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:474039..474106 26863196 MeRIP-seq:(Medium) rs1040617474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4786351,Human_RBP_ID_5102911,Human_RBP_ID_5508052,Human_RBP_ID_7343122,Human_RBP_ID_9160876,Human_RBP_ID_9396840,Human_RBP_ID_18026849,Human_RBP_ID_18424526,Human_RBP_ID_22095311,Human_RBP_ID_26825247,Human_RBP_ID_27068331 76502 RMVar_ID_76502 Human_SNP_ID_170159637 m1A Human chr4 - 474090 474090 474090 GTTAGGGCCTCACTTCCCTGCTTCCACACCTCAGGGAGGCCTCGGTGATTTTGCCAGAGCCTCAG GTTAGGGCCTCACTTCCCTGCTTCCACACCTCCGGGAGGCCTCGGTGATTTTGCCAGAGCCTCAG T G ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:474039..474106 26863196 MeRIP-seq:(Medium) rs1040617474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4786351,Human_RBP_ID_5102911,Human_RBP_ID_5508052,Human_RBP_ID_7343122,Human_RBP_ID_9160876,Human_RBP_ID_9396840,Human_RBP_ID_18026849,Human_RBP_ID_18424526,Human_RBP_ID_22095311,Human_RBP_ID_26825247,Human_RBP_ID_27068331 76503 RMVar_ID_76503 Human_SNP_ID_170171896 m1A Human chr4 + 517031 517030 517032 CATGGGGCGCACATTCAGGGGATGGTCAGAGCAGGGGCCAGAGTGGCAAGGGCAGGGCAGAGGAG CATGGGGCGCACATTCAGGGGATGGTCAGAGC__GGGCCAGAGTGGCAAGGGCAGGGCAGAGGAG CAG C PIGG Ensembl:ENSG00000174227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:517028..517123 26863196 MeRIP-seq:(Medium) rs1284299321 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22726224 RMVar_hsa_circ_4464,RMVar_hsa_circ_69717,RMVar_hsa_circ_113243,RMVar_hsa_circ_224173,RMVar_hsa_circ_12052,RMVar_hsa_circ_76495,RMVar_hsa_circ_79352,RMVar_hsa_circ_224175,RMVar_hsa_circ_11434,RMVar_hsa_circ_224176 76504 RMVar_ID_76504 Human_SNP_ID_170176556 m1A Human chr4 - 532944 532944 532944 GCTCCCAGGCCCCGCCTCTCCACTCCAAGACCACACCCTTCCACTCCTAGGCCCCACCTCTCCAT GCTCCCAGGCCCCGCCTCTCCACTCCAAGACCCCACCCTTCCACTCCTAGGCCCCACCTCTCCAT T G lnc-ZNF721-3 RNACentral:URS00008BC04F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:532638..533139 26863196 MeRIP-seq:(Medium) rs1166925779 Functional Loss SNV dbSNP153 33..33 33 - - - 76505 RMVar_ID_76505 Human_SNP_ID_170218745 m1A Human chr4 - 672519 672519 672519 CATGTGCTTTTCTTCTAACCTTCCGGCCCAAGATGACAGCATATTAAAGTGAGTGACCCTGCGAC CATGTGCTTTTCTTCTAACCTTCCGGCCCAAGGTGACAGCATATTAAAGTGAGTGACCCTGCGAC T C ATP5ME Ensembl:ENSG00000169020 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:672492..672571 26863196 MeRIP-seq:(Medium) rs1131704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942571,Human_RBP_ID_1641582,Human_RBP_ID_5210985,Human_RBP_ID_9395971,Human_RBP_ID_17662037,Human_RBP_ID_18032244,Human_RBP_ID_24060943,Human_RBP_ID_24547860,Human_RBP_ID_26348857,Human_RBP_ID_27508949,Human_RBP_ID_27823905 Human_Splice_Rec_535522,Human_Splice_Rec_535528,Human_Splice_Rec_535532,Human_Splice_Rec_535536,Human_Splice_Rec_535538 RMVar_hsa_circ_83130,RMVar_hsa_circ_103935,RMVar_hsa_circ_224182,RMVar_hsa_circ_224183 76506 RMVar_ID_76506 Human_SNP_ID_170219059 m1A Human chr4 + 673323 673323 673323 TGTCACTCGTACCTTCTGCCAATTCTCTGGCAATCCGTTTCAGTTCATCCTGCTTCTTCTTCTCT TGTCACTCGTACCTTCTGCCAATTCTCTGGCAGTCCGTTTCAGTTCATCCTGCTTCTTCTTCTCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:672484..673466 32194978 MeRIP-seq:(Medium) rs902011351 Functional Loss SNV dbSNP153 33..33 33 - - - 76507 RMVar_ID_76507 Human_SNP_ID_170219116 m1A Human chr4 + 673400 673400 673400 CTCCTCTCCTCTTCTGCCCGAGGTTTTAGGTAATCTGTTTGGCGGAATGCAGGAGAATAAAATTC CTCCTCTCCTCTTCTGCCCGAGGTTTTAGGTACTCTGTTTGGCGGAATGCAGGAGAATAAAATTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr4:673351..673425;chr4:673326..673450 26863196,26863410 MeRIP-seq:(Medium) rs375900377 Functional Loss SNV dbSNP153 33..33 33 - - - 76508 RMVar_ID_76508 Human_SNP_ID_170219203 m1A Human chr4 - 673593 673593 673593 GGACGAGTGAGCCAGTGCGTGAGCGGGTGGGCAGCAGGGGCCCTGTAGCCTCTGGGTTGGACTCG GGACGAGTGAGCCAGTGCGTGAGCGGGTGGGCCGCAGGGGCCCTGTAGCCTCTGGGTTGGACTCG T G ATP5ME Ensembl:ENSG00000169020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:673589..673665 26863196 MeRIP-seq:(Medium) rs920144009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_535529 RMVar_hsa_circ_83130,RMVar_hsa_circ_103935,RMVar_hsa_circ_224182,RMVar_hsa_circ_224183 76509 RMVar_ID_76509 Human_SNP_ID_170219436 m1A Human chr4 - 674145 674145 674145 TGGGCCCCCCCGTGTCCCGCCCCGCAGCTCCGACCCCGCGGGCTGCGACCCCCGGCCCCCGCCCC TGGGCCCCCCCGTGTCCCGCCCCGCAGCTCCGTCCCCGCGGGCTGCGACCCCCGGCCCCCGCCCC T A ATP5ME Ensembl:ENSG00000169020 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:674141..674275 26863196 MeRIP-seq:(Medium) rs1241661873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17089829 RMVar_hsa_circ_83130,RMVar_hsa_circ_224183 76510 RMVar_ID_76510 Human_SNP_ID_170219488 m1A Human chr4 + 674224 674224 674224 GGCTGCAAAGCCTGGATCACCTTGATGAGCGGAGAGACCTGCACCGGTGGCACCATCTTGTCCCT GGCTGCAAAGCCTGGATCACCTTGATGAGCGGGGAGACCTGCACCGGTGGCACCATCTTGTCCCT A G MYL5 Ensembl:ENSG00000215375 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:673871..674325 26863196 MeRIP-seq:(Medium) rs1560148685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19121288,Human_RBP_ID_22745637 76511 RMVar_ID_76511 Human_SNP_ID_170222330 m1A Human chr4 - 681514 681514 681514 AGCGTCGGGGAGGACCGTGTGGGGTCTGGGGGAGGTGCGGGGGTCCTGAGGGGTGGCCCGGCATT AGCGTCGGGGAGGACCGTGTGGGGTCTGGGGGTGGTGCGGGGGTCCTGAGGGGTGGCCCGGCATT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:681468..681576 26863196 MeRIP-seq:(Medium) rs1313125965 Functional Loss SNV dbSNP153 33..33 33 - - - 76512 RMVar_ID_76512 Human_SNP_ID_170231310 m1A Human chr4 - 705867 705867 705867 CCCTCTGGGTCCCCCCCAAGAGGAGGAGAAAAAAGCCCGTCCGGAGTTTAAAACAAAGAGGCGGA CCCTCTGGGTCCCCCCCAAGAGGAGGAGAAAAGAGCCCGTCCGGAGTTTAAAACAAAGAGGCGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:705834..705978;chr4:705824..706063 26863196 MeRIP-seq:(Medium) rs932509762 Functional Loss SNV dbSNP153 33..33 33 - - - 76513 RMVar_ID_76513 Human_SNP_ID_170231781 m1A Human chr4 + 706980 706980 706980 GCAGGACCGCGGGAGGGTAGGGACCCCAGCCCAGGCAGGACCCTGGGAAGGTCGCGACCCCAGCC GCAGGACCGCGGGAGGGTAGGGACCCCAGCCCGGGCAGGACCCTGGGAAGGTCGCGACCCCAGCC A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:706971..707278 26863196 MeRIP-seq:(Medium) rs998260135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15618 76514 RMVar_ID_76514 Human_SNP_ID_170236197 m1A Human chr4 + 719899 719899 719899 CCTTGGCAGTCGGAGCGTCGGGGCCGCATTATAGAGGGAGGGACTCTCCGGACGATGGGAACGAG CCTTGGCAGTCGGAGCGTCGGGGCCGCATTATGGAGGGAGGGACTCTCCGGACGATGGGAACGAG A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:719893..719989 26863196 MeRIP-seq:(Medium) rs1346749766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3748302 RMVar_hsa_circ_15618 76515 RMVar_ID_76515 Human_SNP_ID_170236390 m1A Human chr4 - 720493 720493 720493 GCCATGCACAAGGCTCCCTGGCAGGAGGCCCTACCCACTCACGGGTGGGCCAGCCCCTGTCCACC GCCATGCACAAGGCTCCCTGGCAGGAGGCCCTTCCCACTCACGGGTGGGCCAGCCCCTGTCCACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:720483..720601 26863196 MeRIP-seq:(Medium) rs1227843712 Functional Loss SNV dbSNP153 33..33 33 - - - 76516 RMVar_ID_76516 Human_SNP_ID_170236679 m1A Human chr4 + 721364 721364 721364 CAAGGCTGTCCTAAGATATGGGTGGCAGAAGAAAATGTGCCCCAGGCATGGGCTTGTGATGCCGG CAAGGCTGTCCTAAGATATGGGTGGCAGAAGAGAATGTGCCCCAGGCATGGGCTTGTGATGCCGG A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:721362..722064 26863196 MeRIP-seq:(Medium) rs1560198738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5210072 RMVar_hsa_circ_15618 76517 RMVar_ID_76517 Human_SNP_ID_170236836 m1A Human chr4 - 721834 721834 721834 TCCCACAGGCCTCTTTCCACACCCACATGCAGAGACACCCATCCACCCACCTCCCACAGGCCCCT TCCCACAGGCCTCTTTCCACACCCACATGCAGTGACACCCATCCACCCACCTCCCACAGGCCCCT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:721719..721953 26863196 MeRIP-seq:(Medium) rs1019743238 Functional Loss SNV dbSNP153 33..33 33 - - - 76518 RMVar_ID_76518 Human_SNP_ID_170236837 m1A Human chr4 - 721834 721834 721834 TCCCACAGGCCTCTTTCCACACCCACATGCAGAGACACCCATCCACCCACCTCCCACAGGCCCCT TCCCACAGGCCTCTTTCCACACCCACATGCAGCGACACCCATCCACCCACCTCCCACAGGCCCCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:721719..721953 26863196 MeRIP-seq:(Medium) rs1019743238 Functional Loss SNV dbSNP153 33..33 33 - - - 76519 RMVar_ID_76519 Human_SNP_ID_170237824 m1A Human chr4 + 724153 724153 724153 AGACTCAGGGCAGATGGTGGTTGTCAGCCGGGAGGGGGCACGGAGCCCTGGGGGTGGTCAGGCCC AGACTCAGGGCAGATGGTGGTTGTCAGCCGGGGGGGGGCACGGAGCCCTGGGGGTGGTCAGGCCC A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:724147..724261 26863196 MeRIP-seq:(Medium) rs900730838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836957,Human_RBP_ID_3747571,Human_RBP_ID_5325825,Human_RBP_ID_8129999,Human_RBP_ID_8212127,Human_RBP_ID_8236346,Human_RBP_ID_18955015,Human_RBP_ID_21988412,Human_RBP_ID_22481362,Human_RBP_ID_22726883,Human_RBP_ID_26791327 RMVar_hsa_circ_15618 76520 RMVar_ID_76520 Human_SNP_ID_170241304 m1A Human chr4 + 733771 733771 733771 GCAGCGGGTACCTCATCGACGCCACCACGGTGACCGAGTGTCTGCACACCTGTACGTGCCCTGCC GCAGCGGGTACCTCATCGACGCCACCACGGTGTCCGAGTGTCTGCACACCTGTACGTGCCCTGCC A T PCGF3 Ensembl:ENSG00000185619 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:733765..733903 26863196 MeRIP-seq:(Medium) rs1407893641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623845,Human_RBP_ID_940432,Human_RBP_ID_9396854 Human_Splice_Rec_535748,Human_Splice_Rec_535749,Human_Splice_Rec_535756,Human_Splice_Rec_535757,Human_Splice_Rec_535780,Human_Splice_Rec_535786,Human_Splice_Rec_535787,Human_Splice_Rec_535794,Human_Splice_Rec_535795,Human_Splice_Rec_535802,Human_Splice_Rec_535803,Human_Splice_Rec_535822,Human_Splice_Rec_535823,Human_Splice_Rec_535842,Human_Splice_Rec_535843,Human_Splice_Rec_535854,Human_Splice_Rec_535855,Human_Splice_Rec_535876,Human_Splice_Rec_535877 RMVar_hsa_circ_31864,RMVar_hsa_circ_275725,RMVar_hsa_circ_325760,RMVar_hsa_circ_109182,RMVar_hsa_circ_224185,RMVar_hsa_circ_224186,RMVar_hsa_circ_224188,RMVar_hsa_circ_224187,RMVar_hsa_circ_87621,RMVar_hsa_circ_329377,RMVar_hsa_circ_345456,RMVar_hsa_circ_307009 76521 RMVar_ID_76521 Human_SNP_ID_170245004 m1A Human chr4 + 744654 744651 744654 TTCAAACAAAGAGGCCGCGGAGGAGAAGCCGGAGGAGGACAACGACTACCACCGCAGCGACGAGC TTCAAACAAAGAGGCCGCGGAGGAGAAGCC___GGAGGACAACGACTACCACCGCAGCGACGAGC CGGA C PCGF3 Ensembl:ENSG00000185619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:744556..744728 26863196 MeRIP-seq:(Medium) rs1560210252 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_249212 Human_Splice_Rec_535764,Human_Splice_Rec_535765,Human_Splice_Rec_535810,Human_Splice_Rec_535811,Human_Splice_Rec_535830,Human_Splice_Rec_535831,Human_Splice_Rec_535862,Human_Splice_Rec_535863,Human_Splice_Rec_535884,Human_Splice_Rec_535885 Human_miRNA_ID_2254283 RMVar_hsa_circ_31864,RMVar_hsa_circ_275725,RMVar_hsa_circ_37697,RMVar_hsa_circ_329377,RMVar_hsa_circ_345456,RMVar_hsa_circ_319968,RMVar_hsa_circ_323026,RMVar_hsa_circ_332368,RMVar_hsa_circ_38609,RMVar_hsa_circ_336642,RMVar_hsa_circ_345788,RMVar_hsa_circ_224189 76522 RMVar_ID_76522 Human_SNP_ID_170245596 m1A Human chr4 - 747726 747726 747726 ATTACAGGAGCACTAATACAGGAGTGTCCCGGAGGCCCGGGGCCCCGCCCACCTGCTCACGCCTC ATTACAGGAGCACTAATACAGGAGTGTCCCGGCGGCCCGGGGCCCCGCCCACCTGCTCACGCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:747660..747841 26863196 MeRIP-seq:(Medium) rs1308008640 Functional Loss SNV dbSNP153 33..33 33 - - - 76523 RMVar_ID_76523 Human_SNP_ID_170248084 m1A Human chr4 - 754522 754522 754522 CTACCTCCTGCCTCACCTCTACAGTCCAGGAGAGGCTCTTTCTACCCTCCGCCCCTTCTACCTCC CTACCTCCTGCCTCACCTCTACAGTCCAGGAGTGGCTCTTTCTACCCTCCGCCCCTTCTACCTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:754514..754687 26863196 MeRIP-seq:(Medium) rs926780282 Functional Loss SNV dbSNP153 33..33 33 - - - 76524 RMVar_ID_76524 Human_SNP_ID_170248097 m1A Human chr4 - 754555 754555 754555 ACGTGGGGCAGCCTGGCACCAGGTCCCAGCTCACTACCTCCTGCCTCACCTCTACAGTCCAGGAG ACGTGGGGCAGCCTGGCACCAGGTCCCAGCTCTCTACCTCCTGCCTCACCTCTACAGTCCAGGAG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:754551..754657 26863196 MeRIP-seq:(Medium) rs1365156836 Functional Loss SNV dbSNP153 33..33 33 - - - 76525 RMVar_ID_76525 Human_SNP_ID_170249456 m1A Human chr4 - 758201 758201 758201 GCTTGTGCAGGGAGGGGCACAGACTTACAGTGACTTTGGACTTTTTTTTTTTTTTTTTTTTTTTT GCTTGTGCAGGGAGGGGCACAGACTTACAGTGTCTTTGGACTTTTTTTTTTTTTTTTTTTTTTTT T A lnc-CPLX1-7 RNACentral:URS0000D5894A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:758193..758695 26863196 MeRIP-seq:(Medium) rs1404583959 Functional Loss SNV dbSNP153 33..33 33 - - - 76526 RMVar_ID_76526 Human_SNP_ID_170249465 m1A Human chr4 + 758228 758228 758228 CAAAGTCACTGTAAGTCTGTGCCCCTCCCTGCACAAGCACCCCCACCGCGGCTCTCACCGGGCAC CAAAGTCACTGTAAGTCTGTGCCCCTCCCTGCGCAAGCACCCCCACCGCGGCTCTCACCGGGCAC A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:758225..758702 26863196 MeRIP-seq:(Medium) rs564975997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31864,RMVar_hsa_circ_37697,RMVar_hsa_circ_345456,RMVar_hsa_circ_319968,RMVar_hsa_circ_323026,RMVar_hsa_circ_345788 76527 RMVar_ID_76527 Human_SNP_ID_170249624 m1A Human chr4 - 758474 758474 758474 CCGGAGCGAGAAGAGCTCGGGAGAGGGGCCGCACGGGAAGAAAGACCCGGAGTCCGGAAGGAGAA CCGGAGCGAGAAGAGCTCGGGAGAGGGGCCGCGCGGGAAGAAAGACCCGGAGTCCGGAAGGAGAA T C lnc-CPLX1-7 RNACentral:URS0000D5894A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:758466..758715 26863196 MeRIP-seq:(Medium) rs867651950 Functional Loss SNV dbSNP153 33..33 33 - - - 76528 RMVar_ID_76528 Human_SNP_ID_170249676 m1A Human chr4 - 758538 758538 758538 GAAAGACCCGGAGTCTGGAGGGAGAACTCGGGAGAGGGGCCGCGTGGGGAGAAAGACCCAGAGTC GAAAGACCCGGAGTCTGGAGGGAGAACTCGGGGGAGGGGCCGCGTGGGGAGAAAGACCCAGAGTC T C lnc-CPLX1-7 RNACentral:URS0000D5894A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:758529..758679 26863196 MeRIP-seq:(Medium) rs1375455246 Functional Loss SNV dbSNP153 33..33 33 - - - 76529 RMVar_ID_76529 Human_SNP_ID_170249772 m1A Human chr4 - 758639 758639 758639 AGACCTGGAGTCCGGAAGGAGAAGAACTCGGGAGAGGGGCCGCGCGGGGAGAAAGAACTGGAGTC AGACCTGGAGTCCGGAAGGAGAAGAACTCGGGGGAGGGGCCGCGCGGGGAGAAAGAACTGGAGTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:758448..758679 26863196 MeRIP-seq:(Medium) rs1372205807 Functional Loss SNV dbSNP153 33..33 33 - - - 76530 RMVar_ID_76530 Human_SNP_ID_170250122 m1A Human chr4 + 759952 759952 759952 CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCACGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCGCGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:759947..760077 26863196 MeRIP-seq:(Medium) rs796077687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18955021,Human_RBP_ID_21064190 RMVar_hsa_circ_31864,RMVar_hsa_circ_37697,RMVar_hsa_circ_345456,RMVar_hsa_circ_319968,RMVar_hsa_circ_323026,RMVar_hsa_circ_345788 76531 RMVar_ID_76531 Human_SNP_ID_170250123 m1A Human chr4 + 759952 759952 759952 CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCACGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCTCGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC A T PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:759947..760077 26863196 MeRIP-seq:(Medium) rs796077687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18955021,Human_RBP_ID_21064190 RMVar_hsa_circ_31864,RMVar_hsa_circ_37697,RMVar_hsa_circ_345456,RMVar_hsa_circ_319968,RMVar_hsa_circ_323026,RMVar_hsa_circ_345788 76532 RMVar_ID_76532 Human_SNP_ID_170258952 m1A Human chr4 - 781588 781588 781588 CGGGCTGGCGCCAGCTCAGGAGGACGCCCCGAAGCCGAGGCCTCGGAAGCAGGTTTTTCCCAGAC CGGGCTGGCGCCAGCTCAGGAGGACGCCCCGAGGCCGAGGCCTCGGAAGCAGGTTTTTCCCAGAC T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:781542..781743 26863196 MeRIP-seq:(Medium) rs1314830558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18501116,Human_RBP_ID_22726570 76533 RMVar_ID_76533 Human_SNP_ID_170258974 m1A Human chr4 + 781635 781630 781635 TGAGCTGGCGCCAGCCCGCAGCGGGGCCGGGCAGGGACGCCGGCCTAACGGTGGGGACCGGCAGG TGAGCTGGCGCCAGCCCGCAGCGGGGCC_____GGGACGCCGGCCTAACGGTGGGGACCGGCAGG CGGGCA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:781622..781741 32194978 MeRIP-seq:(Medium) rs1560231461 Functional Loss DEL dbSNP153 29..33 33 - - - 76534 RMVar_ID_76534 Human_SNP_ID_170260499 m1A Human chr4 + 785992 785992 785992 CAGAGACGGATGGACAGGGGCGCGAGGGGGCCAGGCCGGGGGGCGGAGAGCGGCCGCGTGCGGAC CAGAGACGGATGGACAGGGGCGCGAGGGGGCCTGGCCGGGGGGCGGAGAGCGGCCGCGTGCGGAC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:785893..786042 26863410 MeRIP-seq:(Medium) rs1363053791 Functional Loss SNV dbSNP153 33..33 33 - - - 76535 RMVar_ID_76535 Human_SNP_ID_170260859 m1A Human chr4 - 786682 786680 786683 CCCGCCTCCCCCGCAGTACGGCATCAAGAAGAAGGAGGAGCGCGAGGCCGAGGCCCAGGCCGCCA CCCGCCTCCCCCGCAGTACGGCATCAAGAAG___GAGGAGCGCGAGGCCGAGGCCCAGGCCGCCA CCTT C CPLX1 Ensembl:ENSG00000168993 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:786633..792565 26863196 MeRIP-seq:(Medium) rs779856111 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_535910,Human_Splice_Rec_535916,Human_Splice_Rec_535918,Human_Splice_Rec_535922 76536 RMVar_ID_76536 Human_SNP_ID_170260860 m1A Human chr4 - 786682 786682 786682 CCCGCCTCCCCCGCAGTACGGCATCAAGAAGAAGGAGGAGCGCGAGGCCGAGGCCCAGGCCGCCA CCCGCCTCCCCCGCAGTACGGCATCAAGAAGAGGGAGGAGCGCGAGGCCGAGGCCCAGGCCGCCA T C CPLX1 Ensembl:ENSG00000168993 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:786633..792565 26863196 MeRIP-seq:(Medium) rs893261910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_535910,Human_Splice_Rec_535916,Human_Splice_Rec_535918,Human_Splice_Rec_535922 76537 RMVar_ID_76537 Human_SNP_ID_170260864 m1A Human chr4 - 786689 786689 786689 CCTGACCCCCGCCTCCCCCGCAGTACGGCATCAAGAAGAAGGAGGAGCGCGAGGCCGAGGCCCAG CCTGACCCCCGCCTCCCCCGCAGTACGGCATCCAGAAGAAGGAGGAGCGCGAGGCCGAGGCCCAG T G CPLX1 Ensembl:ENSG00000168993 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:786603..786763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_535910,Human_Splice_Rec_535916,Human_Splice_Rec_535918,Human_Splice_Rec_535922 76538 RMVar_ID_76538 Human_SNP_ID_170262989 m1A Human chr4 - 792560 792560 792560 GGGGAAGATGCTGGGGGGTGACGAGGAGAAGGACCCAGACGCCGCCAAGAAGGAGGAGGAGCGGC GGGGAAGATGCTGGGGGGTGACGAGGAGAAGGGCCCAGACGCCGCCAAGAAGGAGGAGGAGCGGC T C CPLX1 Ensembl:ENSG00000168993 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:792466..792653;chr4:786395..792670 26863196 MeRIP-seq:(Medium) rs754069852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_535908,Human_Splice_Rec_535914,Human_Splice_Rec_535920 76539 RMVar_ID_76539 Human_SNP_ID_170271499 m1A Human chr4 - 822304 822304 822304 AGAGATGGGAGCAGAGGGAGAGACAGAGGGATACAGAGAGACAGACAGACAAAGGAAGAGGGCAG AGAGATGGGAGCAGAGGGAGAGACAGAGGGATGCAGAGAGACAGACAGACAAAGGAAGAGGGCAG T C CPLX1 Ensembl:ENSG00000168993 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:822278..822383 26863196 MeRIP-seq:(Medium) rs955251569 Functional Loss SNV dbSNP153 33..33 33 - - - 76540 RMVar_ID_76540 Human_SNP_ID_170272152 m1A Human chr4 + 824555 824555 824555 GGCGATTGCTCTGCTTCCACAGTGGCTCCTCCAGGGGTCAGAACTCACACGCAAGTATGGCCGGG GGCGATTGCTCTGCTTCCACAGTGGCTCCTCCCGGGGTCAGAACTCACACGCAAGTATGGCCGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:824506..826149 26863196 MeRIP-seq:(Medium) rs765619001 Functional Loss SNV dbSNP153 33..33 33 - - - 76541 RMVar_ID_76541 Human_SNP_ID_170272153 m1A Human chr4 + 824555 824555 824555 GGCGATTGCTCTGCTTCCACAGTGGCTCCTCCAGGGGTCAGAACTCACACGCAAGTATGGCCGGG GGCGATTGCTCTGCTTCCACAGTGGCTCCTCCGGGGGTCAGAACTCACACGCAAGTATGGCCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:824506..826149 26863196 MeRIP-seq:(Medium) rs765619001 Functional Loss SNV dbSNP153 33..33 33 - - - 76542 RMVar_ID_76542 Human_SNP_ID_170272158 m1A Human chr4 - 824560 824560 824560 TCGCTCCCGGCCATACTTGCGTGTGAGTTCTGACCCCTGGAGGAGCCACTGTGGAAGCAGAGCAA TCGCTCCCGGCCATACTTGCGTGTGAGTTCTGGCCCCTGGAGGAGCCACTGTGGAAGCAGAGCAA T C CPLX1 Ensembl:ENSG00000168993 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:824428..824640 26863196 MeRIP-seq:(Medium) rs1477523846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_535906,Human_Splice_Rec_535907,Human_Splice_Rec_535912,Human_Splice_Rec_535913 76543 RMVar_ID_76543 Human_SNP_ID_170273030 m1A Human chr4 - 826331 826330 826331 CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCCACCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCC_CCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:826265..826451 26863196 MeRIP-seq:(Medium) rs1304550334 Functional Loss DEL dbSNP153 33..33 33 - - - 76544 RMVar_ID_76544 Human_SNP_ID_170273034 m1A Human chr4 - 826331 826331 826331 CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCCACCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCCGCCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:826265..826451 26863196 MeRIP-seq:(Medium) rs1162046268 Functional Loss SNV dbSNP153 33..33 33 - - - 76545 RMVar_ID_76545 Human_SNP_ID_170273035 m1A Human chr4 - 826331 826331 826331 CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCCACCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC CGCCCCCGCCCCCCGCCCCCGCCCCCGGGTCCCCCCCCCGCCCCCGCCCCGGGTCCACCCCCCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:826265..826451 26863196 MeRIP-seq:(Medium) rs1162046268 Functional Loss SNV dbSNP153 33..33 33 - - - 76546 RMVar_ID_76546 Human_SNP_ID_170281453 m1A Human chr4 + 851801 851801 851801 CCCCCGCTCCTCCCGCGCCCCGATCACACTGAAGTTCGAGGCATAGTTAGGCCTTGGCTGTGTGC CCCCCGCTCCTCCCGCGCCCCGATCACACTGACGTTCGAGGCATAGTTAGGCCTTGGCTGTGTGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:851735..851985 32194978 MeRIP-seq:(Medium) rs745811697 Functional Loss SNV dbSNP153 33..33 33 - - - 76547 RMVar_ID_76547 Human_SNP_ID_170281454 m1A Human chr4 + 851801 851801 851801 CCCCCGCTCCTCCCGCGCCCCGATCACACTGAAGTTCGAGGCATAGTTAGGCCTTGGCTGTGTGC CCCCCGCTCCTCCCGCGCCCCGATCACACTGAGGTTCGAGGCATAGTTAGGCCTTGGCTGTGTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:851735..851985 32194978 MeRIP-seq:(Medium) rs745811697 Functional Loss SNV dbSNP153 33..33 33 - - - 76548 RMVar_ID_76548 Human_SNP_ID_170283040 m1A Human chr4 - 856273 856271 856273 TGAGCAGGGGTGAGCAGCTGTGGTGAGGTGTGAGCAGTTGTGAGCAGCTGTGGTGAGCAGGTGTG TGAGCAGGGGTGAGCAGCTGTGGTGAGGTGTG__CAGTTGTGAGCAGCTGTGGTGAGCAGGTGTG GCT G GAK Ensembl:ENSG00000178950 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:856226..856298 26863196 MeRIP-seq:(Medium) rs1407309126 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5426591,Human_RBP_ID_5475776,Human_RBP_ID_7333865,Human_RBP_ID_24067399 RMVar_hsa_circ_83271,RMVar_hsa_circ_97063,RMVar_hsa_circ_224192,RMVar_hsa_circ_224193,RMVar_hsa_circ_330360,RMVar_hsa_circ_28611,RMVar_hsa_circ_354507 76549 RMVar_ID_76549 Human_SNP_ID_170283193 m1A Human chr4 + 856475 856460 856476 CTGCTCACTACAGCTGCTCACCACAGCTGCTCACCACCACAGCTGCTCACACCTACTCACCACCA CTGCTCACTACAGCTGCT________________CACCACAGCTGCTCACACCTACTCACCACCA TCACCACAGCTGCTCAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:856428..856605 26863196 MeRIP-seq:(Medium) rs1412491057 Functional Loss DEL dbSNP153 19..34 33 - - - 76550 RMVar_ID_76550 Human_SNP_ID_170283202 m1A Human chr4 + 856475 856473 856476 CTGCTCACTACAGCTGCTCACCACAGCTGCTCACCACCACAGCTGCTCACACCTACTCACCACCA CTGCTCACTACAGCTGCTCACCACAGCTGCT___CACCACAGCTGCTCACACCTACTCACCACCA TCAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:856428..856605 26863196 MeRIP-seq:(Medium) rs1277434123 Functional Loss DEL dbSNP153 32..34 33 - - - 76551 RMVar_ID_76551 Human_SNP_ID_170286210 m1A Human chr4 - 865246 865246 865246 CAAACTGTGCTCTCTTCTGGTTCCTTCTTCCCAGGGGATCTGCCAGGAGAGCCCAGCAAGATGAC CAAACTGTGCTCTCTTCTGGTTCCTTCTTCCCTGGGGATCTGCCAGGAGAGCCCAGCAAGATGAC T A GAK Ensembl:ENSG00000178950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:859411..866391 32194978 MeRIP-seq:(Medium) rs113215101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940442,Human_RBP_ID_19014066 RMVar_hsa_circ_16602,RMVar_hsa_circ_83271,RMVar_hsa_circ_97063,RMVar_hsa_circ_224192,RMVar_hsa_circ_224193,RMVar_hsa_circ_330360,RMVar_hsa_circ_71279,RMVar_hsa_circ_28611,RMVar_hsa_circ_267748,RMVar_hsa_circ_124938,RMVar_hsa_circ_265724,RMVar_hsa_circ_268309,RMVar_hsa_circ_115562,RMVar_hsa_circ_224194,RMVar_hsa_circ_224195 76552 RMVar_ID_76552 Human_SNP_ID_170286211 m1A Human chr4 - 865246 865246 865246 CAAACTGTGCTCTCTTCTGGTTCCTTCTTCCCAGGGGATCTGCCAGGAGAGCCCAGCAAGATGAC CAAACTGTGCTCTCTTCTGGTTCCTTCTTCCCGGGGGATCTGCCAGGAGAGCCCAGCAAGATGAC T C GAK Ensembl:ENSG00000178950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:859411..866391 32194978 MeRIP-seq:(Medium) rs113215101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940442,Human_RBP_ID_19014066 RMVar_hsa_circ_16602,RMVar_hsa_circ_83271,RMVar_hsa_circ_97063,RMVar_hsa_circ_224192,RMVar_hsa_circ_224193,RMVar_hsa_circ_330360,RMVar_hsa_circ_71279,RMVar_hsa_circ_28611,RMVar_hsa_circ_267748,RMVar_hsa_circ_124938,RMVar_hsa_circ_265724,RMVar_hsa_circ_268309,RMVar_hsa_circ_115562,RMVar_hsa_circ_224194,RMVar_hsa_circ_224195 76553 RMVar_ID_76553 Human_SNP_ID_170286573 m1A Human chr4 + 866347 866347 866347 CTGAGGGAGGCGGCCATGGAGAGCTGGCTGCCAGGCGAGAGGCACTTACCCAGGTGCAGGAAGTC CTGAGGGAGGCGGCCATGGAGAGCTGGCTGCCGGGCGAGAGGCACTTACCCAGGTGCAGGAAGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:866345..866535 26863196 MeRIP-seq:(Medium) rs1267245089 Functional Loss SNV dbSNP153 33..33 33 - - - 76554 RMVar_ID_76554 Human_SNP_ID_170293998 m1A Human chr4 - 886625 886624 886626 GTGAGAGTGATGTTGGGATCAGAGTGGAAACAAGACAGAGAGGATGCGGCAGCAAAGCCATAAGT GTGAGAGTGATGTTGGGATCAGAGTGGAAAC__GACAGAGAGGATGCGGCAGCAAAGCCATAAGT CTT C GAK Ensembl:ENSG00000178950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:886623..886724 32194978 MeRIP-seq:(Medium) rs1323901360 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1641242,Human_RBP_ID_8596014,Human_RBP_ID_15219905,Human_RBP_ID_24068718 RMVar_hsa_circ_330360,RMVar_hsa_circ_28611,RMVar_hsa_circ_63502,RMVar_hsa_circ_28170,RMVar_hsa_circ_224198,RMVar_hsa_circ_377830,RMVar_hsa_circ_364435,RMVar_hsa_circ_99397,RMVar_hsa_circ_9661,RMVar_hsa_circ_25019,RMVar_hsa_circ_224202,RMVar_hsa_circ_319770,RMVar_hsa_circ_224203 76555 RMVar_ID_76555 Human_SNP_ID_170295115 m1A Human chr4 + 888967 888967 888967 CGCCATACGGCTGGTCGTACTCCGCCAGCGCCAGGCCTGCAGGGAGACACAGTCTCAGCAGGCCC CGCCATACGGCTGGTCGTACTCCGCCAGCGCCGGGCCTGCAGGGAGACACAGTCTCAGCAGGCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:888916..893481 32194978 MeRIP-seq:(Medium) rs1363687745 Functional Loss SNV dbSNP153 33..33 33 - - - 76556 RMVar_ID_76556 Human_SNP_ID_170301186 m1A Human chr4 + 905452 905426 905453 ACGCTACAGACTCTGCCACGCCGCGCCACGCTAGGGGCTCCGCCACGCCCCATGCCATGCTACGG ACGCTAC___________________________GGGCTCCGCCACGCCCCATGCCATGCTACGG CAGACTCTGCCACGCCGCGCCACGCTAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:905450..905548 26863196 MeRIP-seq:(Medium) rs1278507758 Functional Loss DEL dbSNP153 8..34 33 - - - 76557 RMVar_ID_76557 Human_SNP_ID_170303817 m1A Human chr4 - 913646 913646 913646 TAATTTTCAGGAGGGTTTGCATTTGTGTATGAAGCTCAAGATGTGGGGAGTGGCAGAGAGTATGC TAATTTTCAGGAGGGTTTGCATTTGTGTATGACGCTCAAGATGTGGGGAGTGGCAGAGAGTATGC T G GAK Ensembl:ENSG00000178950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:913626..913675 26863196 MeRIP-seq:(Medium) rs1214758372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72184,Human_RBP_ID_1982061,Human_RBP_ID_2864921,Human_RBP_ID_3966490,Human_RBP_ID_19121312,Human_RBP_ID_24069882 Human_Splice_Rec_535934,Human_Splice_Rec_535935,Human_Splice_Rec_536120,Human_Splice_Rec_536121,Human_Splice_Rec_536142,Human_Splice_Rec_536143,Human_Splice_Rec_536150,Human_Splice_Rec_536151,Human_Splice_Rec_536156,Human_Splice_Rec_536157,Human_Splice_Rec_536164,Human_Splice_Rec_536165,Human_Splice_Rec_536172,Human_Splice_Rec_536173,Human_Splice_Rec_536177,Human_Splice_Rec_536182,Human_Splice_Rec_536183,Human_Splice_Rec_536188,Human_Splice_Rec_536189 RMVar_hsa_circ_224207,RMVar_hsa_circ_324851,RMVar_hsa_circ_224210,RMVar_hsa_circ_301819,RMVar_hsa_circ_270149,RMVar_hsa_circ_224211 76558 RMVar_ID_76558 Human_SNP_ID_170308279 m1A Human chr4 + 927041 927041 927041 CGCTCCGCACTGCCCCGCACCCCTCCCCGCTCACCTGCGCTCCGCACTGCCCCGCACCCCTTCCC CGCTCCGCACTGCCCCGCACCCCTCCCCGCTCGCCTGCGCTCCGCACTGCCCCGCACCCCTTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:927039..927134 26863196 MeRIP-seq:(Medium) rs1261388051 Functional Loss SNV dbSNP153 33..33 33 - - - 76559 RMVar_ID_76559 Human_SNP_ID_170308291 m1A Human chr4 + 927064 927064 927064 TCCCCGCTCACCTGCGCTCCGCACTGCCCCGCACCCCTTCCCGCTCACCTGCAGTCCGCACTGCC TCCCCGCTCACCTGCGCTCCGCACTGCCCCGCCCCCCTTCCCGCTCACCTGCAGTCCGCACTGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:927057..927129 26863196 MeRIP-seq:(Medium) rs1159093510 Functional Loss SNV dbSNP153 33..33 33 - - - 76560 RMVar_ID_76560 Human_SNP_ID_170309412 m1A Human chr4 - 930879 930879 930879 GCCTGCTCTGTGACCAGACAGGAGACTATCCCAGAATTCTGATTATCACAAAAGGCCTGCGGAGA GCCTGCTCTGTGACCAGACAGGAGACTATCCCGGAATTCTGATTATCACAAAAGGCCTGCGGAGA T C GAK Ensembl:ENSG00000178950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:930876..930999 32194978 MeRIP-seq:(Medium) rs754097400 Functional Loss SNV dbSNP153 33..33 33 - - - 76561 RMVar_ID_76561 Human_SNP_ID_170309817 m1A Human chr4 - 932112 932112 932112 GCTCCCTGGGCGGTGCTTCCGGCCGCGACCAGAGTGACTTCGTGGGGCAGACGGTGGAACTGGGC GCTCCCTGGGCGGTGCTTCCGGCCGCGACCAGTGTGACTTCGTGGGGCAGACGGTGGAACTGGGC T A GAK Ensembl:ENSG00000178950 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:931737..932318 26863196 MeRIP-seq:(Medium) rs373555101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334490,Human_RBP_ID_18827957 Human_Splice_Rec_535933,Human_Splice_Rec_536023,Human_Splice_Rec_536119,Human_Splice_Rec_536137,Human_Splice_Rec_536141,Human_Splice_Rec_536149,Human_Splice_Rec_536181,Human_Splice_Rec_536187 Human_miRNA_ID_650928 76562 RMVar_ID_76562 Human_SNP_ID_170309863 m1A Human chr4 - 932197 932197 932197 CCGACCACTCCGGCTGCCGCGGGGTGCGGCGCAGCCACCGCCATGTCGCTGCTGCAGTCGGCGCT CCGACCACTCCGGCTGCCGCGGGGTGCGGCGCGGCCACCGCCATGTCGCTGCTGCAGTCGGCGCT T C GAK Ensembl:ENSG00000178950 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:932146..932268 26863196 MeRIP-seq:(Medium) rs747682097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794482 76563 RMVar_ID_76563 Human_SNP_ID_170309864 m1A Human chr4 - 932197 932197 932197 CCGACCACTCCGGCTGCCGCGGGGTGCGGCGCAGCCACCGCCATGTCGCTGCTGCAGTCGGCGCT CCGACCACTCCGGCTGCCGCGGGGTGCGGCGCCGCCACCGCCATGTCGCTGCTGCAGTCGGCGCT T G GAK Ensembl:ENSG00000178950 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:932146..932268 26863196 MeRIP-seq:(Medium) rs747682097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794482 76564 RMVar_ID_76564 Human_SNP_ID_170319010 m1A Human chr4 - 960933 960933 960933 CTGGCATGGCCGGCTGCGGCCAGGGAGCACTGACTCCGGGAGGGTGCCTGCTTCAGAGGAGGGCT CTGGCATGGCCGGCTGCGGCCAGGGAGCACTGCCTCCGGGAGGGTGCCTGCTTCAGAGGAGGGCT T G DGKQ Ensembl:ENSG00000145214 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:960908..961003 26863196 MeRIP-seq:(Medium) rs1383752070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19121316 76565 RMVar_ID_76565 Human_SNP_ID_170328729 m1A Human chr4 - 987086 987086 987086 CCAGCAGCGCGGCGCGGGGGCGCAGGGGACGCATGGCCACGCGTGCTCGGGGACTGCGGGGCTTC CCAGCAGCGCGGCGCGGGGGCGCAGGGGACGCGTGGCCACGCGTGCTCGGGGACTGCGGGGCTTC T C SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:987058..987278 26863196 MeRIP-seq:(Medium) rs753767675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212152,Human_RBP_ID_9354486 76566 RMVar_ID_76566 Human_SNP_ID_170328783 m1A Human chr4 - 987137 987137 987137 GGGCCTCGGCCGGGGCCACCGGGGGCGCGGCCAGGAGCGAGGCCAGGAGCGCCAGCAGCGCGGCG GGGCCTCGGCCGGGGCCACCGGGGGCGCGGCCGGGAGCGAGGCCAGGAGCGCCAGCAGCGCGGCG T C SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:987098..987228;chr4:987059..987247 26863196 MeRIP-seq:(Medium) rs794726878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354486 Clinvar_Rec_351 76567 RMVar_ID_76567 Human_SNP_ID_170328801 m1A Human chr4 - 987152 987152 987152 CATGCACCAGGTGCGGGGCCTCGGCCGGGGCCACCGGGGGCGCGGCCAGGAGCGAGGCCAGGAGC CATGCACCAGGTGCGGGGCCTCGGCCGGGGCCCCCGGGGGCGCGGCCAGGAGCGAGGCCAGGAGC T G SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:987051..987175 26863410 MeRIP-seq:(Medium) rs1383976462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354486 76568 RMVar_ID_76568 Human_SNP_ID_170328845 m1A Human chr4 - 987205 987205 987205 GCCTGTGCTCCTCCAGAAGCGCCGCAGGGGCCACAGCGCGCGGGCCGCGTCCACATGCACCAGGT GCCTGTGCTCCTCCAGAAGCGCCGCAGGGGCCTCAGCGCGCGGGCCGCGTCCACATGCACCAGGT T A SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:987107..987212 26863410 MeRIP-seq:(Medium) rs1302843483 Functional Loss SNV dbSNP153 33..33 33 - - - 76569 RMVar_ID_76569 Human_SNP_ID_170328846 m1A Human chr4 - 987205 987205 987205 GCCTGTGCTCCTCCAGAAGCGCCGCAGGGGCCACAGCGCGCGGGCCGCGTCCACATGCACCAGGT GCCTGTGCTCCTCCAGAAGCGCCGCAGGGGCCGCAGCGCGCGGGCCGCGTCCACATGCACCAGGT T C SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:987107..987212 26863410 MeRIP-seq:(Medium) rs1302843483 Functional Loss SNV dbSNP153 33..33 33 - - - 76570 RMVar_ID_76570 Human_SNP_ID_170330215 m1A Human chr4 - 990197 990197 990197 CGCGGCACCAGGGGCCCGGCATGGTGGTCCTCACATGGCTGAGCCTGCTGCGCGGCGCCGGGCAG CGCGGCACCAGGGGCCCGGCATGGTGGTCCTCCCATGGCTGAGCCTGCTGCGCGGCGCCGGGCAG T G SLC26A1 Ensembl:ENSG00000145217 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:990188..990380 26863196 MeRIP-seq:(Medium) rs755828368 Functional Loss SNV dbSNP153 33..33 33 - - - 76571 RMVar_ID_76571 Human_SNP_ID_170334112 m1A Human chr4 - 1001037 1001037 1001037 AGCAGCCTGCGTGATAGGGGTGCAACCTGCCCAGGAGTACCCCCGCCCCGGCCAGGGCCCCAGGG AGCAGCCTGCGTGATAGGGGTGCAACCTGCCCGGGAGTACCCCCGCCCCGGCCAGGGCCCCAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1000993..1001107 26863196 MeRIP-seq:(Medium) rs753108192 Functional Loss SNV dbSNP153 33..33 33 - - - 76572 RMVar_ID_76572 Human_SNP_ID_170334394 m1A Human chr4 + 1001661 1001661 1001661 AAGCCGCTCATCCCCAGGGCAGGTGTAGACGCAGTGCTCCCCCGGCCCAGGCTTCCTGAACTACT AAGCCGCTCATCCCCAGGGCAGGTGTAGACGCGGTGCTCCCCCGGCCCAGGCTTCCTGAACTACT A G IDUA Ensembl:ENSG00000127415 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:1001653..1001785 26863196 MeRIP-seq:(Medium) rs1201137456 Functional Loss SNV dbSNP153 33..33 33 - - - 76573 RMVar_ID_76573 Human_SNP_ID_170334448 m1A Human chr4 - 1001742 1001742 1001742 GTGGGGTGTGGAAGGAGTCGCCGGGGCCTCCCAGCCGCAGGGCGGGGCTGGCGGCGCGCAGACCC GTGGGGTGTGGAAGGAGTCGCCGGGGCCTCCCGGCCGCAGGGCGGGGCTGGCGGCGCGCAGACCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1001698..1001857 26863196 MeRIP-seq:(Medium) rs869025584 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_352 76574 RMVar_ID_76574 Human_SNP_ID_170338429 m1A Human chr4 - 1011682 1011682 1011682 GGCCGGGGCCGGGATCCCGGGGCGGCGGGGCGAGGGGCCCGGGGCGCCGCGCCGCGAGGCGTCCT GGCCGGGGCCGGGATCCCGGGGCGGCGGGGCGGGGGGCCCGGGGCGCCGCGCCGCGAGGCGTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1011626..1011983 26863196 MeRIP-seq:(Medium) rs1186484318 Functional Loss SNV dbSNP153 33..33 33 - - - 76575 RMVar_ID_76575 Human_SNP_ID_170338463 m1A Human chr4 - 1011751 1011751 1011751 CGGGCTCGGGCGCTCGGGGCGCGGGGTCCCGGACCGGGCAGGCGGCGGGGGCGAGTCCGCGGGGC CGGGCTCGGGCGCTCGGGGCGCGGGGTCCCGGGCCGGGCAGGCGGCGGGGGCGAGTCCGCGGGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr4:1011651..1011975;chr4:1011651..1011775 26863410 MeRIP-seq:(Medium) rs1445180170 Functional Loss SNV dbSNP153 33..33 33 - - - 76576 RMVar_ID_76576 Human_SNP_ID_170338464 m1A Human chr4 - 1011751 1011751 1011751 CGGGCTCGGGCGCTCGGGGCGCGGGGTCCCGGACCGGGCAGGCGGCGGGGGCGAGTCCGCGGGGC CGGGCTCGGGCGCTCGGGGCGCGGGGTCCCGGCCCGGGCAGGCGGCGGGGGCGAGTCCGCGGGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr4:1011651..1011975;chr4:1011651..1011775 26863410 MeRIP-seq:(Medium) rs1445180170 Functional Loss SNV dbSNP153 33..33 33 - - - 76577 RMVar_ID_76577 Human_SNP_ID_170338516 m1A Human chr4 - 1011867 1011857 1011867 CGCTCCGCGGTCATCGCCGCCCCGGGCGCCGCATCCCGCCGCCCCGCGCCCCCGGGCCCGGTCTC CGCTCCGCGGTCATCGCCGCCCCGGGCGCCGC__________CCCGCGCCCCCGGGCCCGGTCTC GGCGGCGGGAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1011648..1012005 26863196 MeRIP-seq:(Medium) rs1354296090 Functional Loss DEL dbSNP153 33..42 33 - - - 76578 RMVar_ID_76578 Human_SNP_ID_170338822 m1A Human chr4 + 1012431 1012431 1012431 GCGGCCCGGGACCGGGGAGGGCGGTATCTCCCAGTTCCACGTGTTAGTGACGGCGCCCCCAATGT GCGGCCCGGGACCGGGGAGGGCGGTATCTCCCGGTTCCACGTGTTAGTGACGGCGCCCCCAATGT A G FGFRL1 Ensembl:ENSG00000127418 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1012428..1012615 26863196 MeRIP-seq:(Medium) rs1007662513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115423,RMVar_hsa_circ_224221 76579 RMVar_ID_76579 Human_SNP_ID_170338868 m1A Human chr4 + 1012489 1012489 1012489 CCAATGTCCCCAGGTCCGGACAGGCCGAGATGACGCCGAGCCCCCTGTTGCTGCTCCTGCTGCCG CCAATGTCCCCAGGTCCGGACAGGCCGAGATGGCGCCGAGCCCCCTGTTGCTGCTCCTGCTGCCG A G FGFRL1 Ensembl:ENSG00000127418 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:1012451..1012525 26863196 MeRIP-seq:(Medium) rs1560556409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4768154 Human_Splice_Rec_536762,Human_Splice_Rec_536763,Human_Splice_Rec_536774,Human_Splice_Rec_536775,Human_Splice_Rec_536786,Human_Splice_Rec_536787,Human_Splice_Rec_536797,Human_Splice_Rec_536800,Human_Splice_Rec_536801,Human_Splice_Rec_536807 Human_miRNA_ID_2017653 RMVar_hsa_circ_115423,RMVar_hsa_circ_75612,RMVar_hsa_circ_224221,RMVar_hsa_circ_224222 76580 RMVar_ID_76580 Human_SNP_ID_170343251 m1A Human chr4 + 1023930 1023930 1023930 GCGTGGCCAGCGGGCACCCTCGGCCCGACATCACGTGGATGAAGGACGACCAGGCCTTGACGCGC GCGTGGCCAGCGGGCACCCTCGGCCCGACATCTCGTGGATGAAGGACGACCAGGCCTTGACGCGC A T FGFRL1 Ensembl:ENSG00000127418 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1023880..1023974 26863196 MeRIP-seq:(Medium) rs773123389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4768361,Human_RBP_ID_5475899 RMVar_hsa_circ_97374,RMVar_hsa_circ_115423,RMVar_hsa_circ_75612,RMVar_hsa_circ_224221,RMVar_hsa_circ_224222,RMVar_hsa_circ_224223 76581 RMVar_ID_76581 Human_SNP_ID_170344095 m1A Human chr4 + 1025371 1025371 1025371 CAGTGCTAGACGGCACCGTATCTGCAGTGGGCACGGGGGGGCCGGCCAGACAGGCAGACTGGGAG CAGTGCTAGACGGCACCGTATCTGCAGTGGGCGCGGGGGGGCCGGCCAGACAGGCAGACTGGGAG A G FGFRL1 Ensembl:ENSG00000127418 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1025325..1025547 26863196 MeRIP-seq:(Medium) rs1245196613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213004,Human_RBP_ID_5121280,Human_RBP_ID_9435894,Human_RBP_ID_17525638,Human_RBP_ID_17662166 RMVar_hsa_circ_97374,RMVar_hsa_circ_115423,RMVar_hsa_circ_75612,RMVar_hsa_circ_224221,RMVar_hsa_circ_224222,RMVar_hsa_circ_95312,RMVar_hsa_circ_224223,RMVar_hsa_circ_224224 76582 RMVar_ID_76582 Human_SNP_ID_170352141 m1A Human chr4 - 1046358 1046348 1046359 GGGCTCGGGGAGGGCTGCGGAAAGGCTCGGGAAGGGCTCGGGGAGGGCTGGGGAAGGGCTGGGGA GGGCTCGGGGAGGGCTGCGGAAAGGCTCGGG___________GAGGGCTGGGGAAGGGCTGGGGA CCCCGAGCCCTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1046351..1046431 26863196 MeRIP-seq:(Medium) rs1468563496 Functional Loss DEL dbSNP153 32..42 33 - - - 76583 RMVar_ID_76583 Human_SNP_ID_170352277 m1A Human chr4 - 1046574 1046563 1046574 CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGACTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGG___________GCTCGGGAAGGGCTCGGGAAGG CCATTCCCGAGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1046566..1046650 26863196 MeRIP-seq:(Medium) rs201009383 Functional Loss DEL dbSNP153 33..43 33 - - - 76584 RMVar_ID_76584 Human_SNP_ID_170352288 m1A Human chr4 - 1046574 1046574 1046574 CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGACTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGTCTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1046566..1046650 26863196 MeRIP-seq:(Medium) rs111066682 Functional Loss SNV dbSNP153 33..33 33 - - - 76585 RMVar_ID_76585 Human_SNP_ID_170352289 m1A Human chr4 - 1046574 1046574 1046574 CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGACTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGGCTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1046566..1046650 26863196 MeRIP-seq:(Medium) rs111066682 Functional Loss SNV dbSNP153 33..33 33 - - - 76586 RMVar_ID_76586 Human_SNP_ID_170352290 m1A Human chr4 - 1046574 1046574 1046574 CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGACTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGCCTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1046566..1046650 26863196 MeRIP-seq:(Medium) rs111066682 Functional Loss SNV dbSNP153 33..33 33 - - - 76587 RMVar_ID_76587 Human_SNP_ID_170386799 m1A Human chr4 - 1167270 1167270 1167270 CGGGCATTGGGAAACAGCCTCCTCCTTTCCCAACCTTGCTTCTTAGGGGCCCCCGTGTCCCGTCT CGGGCATTGGGAAACAGCCTCCTCCTTTCCCAGCCTTGCTTCTTAGGGGCCCCCGTGTCCCGTCT T C SPON2 Ensembl:ENSG00000159674 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1167220..1167299 26863196 MeRIP-seq:(Medium) rs916322013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80155,RMVar_hsa_circ_224229 76588 RMVar_ID_76588 Human_SNP_ID_170387459 m1A Human chr4 + 1168980 1168980 1168980 CCCTTGTGGGCGGTGGTCTGTGCTCCGTCCCCACTGCCCACTCTGGTCCCTCGGCTGGCACAGCT CCCTTGTGGGCGGTGGTCTGTGCTCCGTCCCCTCTGCCCACTCTGGTCCCTCGGCTGGCACAGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1168975..1169157 26863196 MeRIP-seq:(Medium) rs1337925703 Functional Loss SNV dbSNP153 33..33 33 - - - 76589 RMVar_ID_76589 Human_SNP_ID_170388505 m1A Human chr4 - 1171379 1171379 1171379 AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGATCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGTTCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG T A SPON2 Ensembl:ENSG00000159674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:1171331..1171411;chr4:1171328..1171422 26863196 MeRIP-seq:(Medium) rs749838094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22770925 RMVar_hsa_circ_80155,RMVar_hsa_circ_224229 76590 RMVar_ID_76590 Human_SNP_ID_170388506 m1A Human chr4 - 1171379 1171379 1171379 AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGATCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGGTCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG T C SPON2 Ensembl:ENSG00000159674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:1171331..1171411;chr4:1171328..1171422 26863196 MeRIP-seq:(Medium) rs749838094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22770925 RMVar_hsa_circ_80155,RMVar_hsa_circ_224229 76591 RMVar_ID_76591 Human_SNP_ID_170388797 m1A Human chr4 - 1171942 1171942 1171942 CCATCTGTTCCGCCAGAGCCCTGGCCAAATACAGCATCACCTTCACGGGCAAGTGGAGCCAGACG CCATCTGTTCCGCCAGAGCCCTGGCCAAATACGGCATCACCTTCACGGGCAAGTGGAGCCAGACG T C SPON2 Ensembl:ENSG00000159674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1171831..1172012 26863196 MeRIP-seq:(Medium) rs1355511112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795222 Human_Splice_Rec_536989,Human_Splice_Rec_537001,Human_Splice_Rec_537015,Human_Splice_Rec_537031,Human_Splice_Rec_537033 76592 RMVar_ID_76592 Human_SNP_ID_170389072 m1A Human chr4 - 1172732 1172732 1172732 GTTGGGAAAGCGGCAGCCCCCGCCGCCCCCGCAGCCCCTTCTCCTCCTTTCTCCCACGTCCTATC GTTGGGAAAGCGGCAGCCCCCGCCGCCCCCGCCGCCCCTTCTCCTCCTTTCTCCCACGTCCTATC T G SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1172696..1172797 26863196 MeRIP-seq:(Medium) rs1330941567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786586,Human_RBP_ID_940465,Human_RBP_ID_4794503 76593 RMVar_ID_76593 Human_SNP_ID_170390933 m1A Human chr4 - 1178483 1178483 1178483 GCCAGGGAGGAAGTCAGCGGGTGCTGAAGAGGAGGGACAGAGGAGAGTGGGGCGGGAAGAGCCAC GCCAGGGAGGAAGTCAGCGGGTGCTGAAGAGGTGGGACAGAGGAGAGTGGGGCGGGAAGAGCCAC T A SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1178444..1178568 26863196 MeRIP-seq:(Medium) rs1380735267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3747691,Human_RBP_ID_22726924 76594 RMVar_ID_76594 Human_SNP_ID_170400736 m1A Human chr4 - 1211623 1211623 1211623 CAGCTCCAAAAGGAAAAGCTTGGGCGGTGCCCAGCGTGCCCGCTGCCCATCGACGTCTGTCCTGG CAGCTCCAAAAGGAAAAGCTTGGGCGGTGCCCCGCGTGCCCGCTGCCCATCGACGTCTGTCCTGG T G CTBP1 Ensembl:ENSG00000159692 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1211576..1211650 32194978 MeRIP-seq:(Medium) rs879622540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_612254,Human_RBP_ID_4771255,Human_RBP_ID_5120945,Human_RBP_ID_15033935,Human_RBP_ID_18817717,Human_RBP_ID_24032926 76595 RMVar_ID_76595 Human_SNP_ID_170404997 m1A Human chr4 - 1224252 1224244 1224253 GTCACAGCACACACACACGGGTATCACATGGCACACATGGGCACCACACATGGATATCACACCAT GTCACAGCACACACACACGGGTATCACATGG_________GCACCACACATGGATATCACACCAT CCCATGTGTG C CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1224250..1224320 26863196 MeRIP-seq:(Medium) rs1415652432 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_213024,Human_RBP_ID_266683,Human_RBP_ID_1069265,Human_RBP_ID_2815449,Human_RBP_ID_9435708,Human_RBP_ID_24535751,Human_RBP_ID_24554185,Human_RBP_ID_26763530,Human_RBP_ID_26825265 RMVar_hsa_circ_6559,RMVar_hsa_circ_15712,RMVar_hsa_circ_306179,RMVar_hsa_circ_33217,RMVar_hsa_circ_334775,RMVar_hsa_circ_21874 76596 RMVar_ID_76596 Human_SNP_ID_170406550 m1A Human chr4 + 1228162 1228162 1228162 CCATGGACGAAGCAAGACGGGACGGAGCTTGCATGAATGGGCACAGGAGAGAACTCGGAGCCGGC CCATGGACGAAGCAAGACGGGACGGAGCTTGCGTGAATGGGCACAGGAGAGAACTCGGAGCCGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1228159..1228389 26863196 MeRIP-seq:(Medium) rs1359266010 Functional Loss SNV dbSNP153 33..33 33 - - - 76597 RMVar_ID_76597 Human_SNP_ID_170408863 m1A Human chr4 - 1235033 1235033 1235033 GTCCCTGCCACACCCTGGGTGATCTCGGCAGCATGATGGCGAGTGAAGAAGCTGGTTTCAAGGGG GTCCCTGCCACACCCTGGGTGATCTCGGCAGCGTGATGGCGAGTGAAGAAGCTGGTTTCAAGGGG T C CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1235031..1235139 32194978 MeRIP-seq:(Medium) rs1036290679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306179,RMVar_hsa_circ_334775,RMVar_hsa_circ_21874,RMVar_hsa_circ_224234,RMVar_hsa_circ_224231,RMVar_hsa_circ_282062,RMVar_hsa_circ_286412,RMVar_hsa_circ_101054,RMVar_hsa_circ_308822,RMVar_hsa_circ_224230,RMVar_hsa_circ_272666,RMVar_hsa_circ_224236,RMVar_hsa_circ_224235 76598 RMVar_ID_76598 Human_SNP_ID_170409014 m1A Human chr4 - 1235450 1235450 1235450 GGGCGAGATGAGGAAGGGTCGCTCTTGCAGAAACTTCAGAACAGGAGAGGGAAGGGGTTGGAAGT GGGCGAGATGAGGAAGGGTCGCTCTTGCAGAAGCTTCAGAACAGGAGAGGGAAGGGGTTGGAAGT T C CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1235447..1235561 26863196 MeRIP-seq:(Medium) rs897597431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11666,Human_RBP_ID_22526863,Human_RBP_ID_22726341,Human_RBP_ID_26349730 RMVar_hsa_circ_306179,RMVar_hsa_circ_334775,RMVar_hsa_circ_21874,RMVar_hsa_circ_224234,RMVar_hsa_circ_224231,RMVar_hsa_circ_282062,RMVar_hsa_circ_286412,RMVar_hsa_circ_101054,RMVar_hsa_circ_308822,RMVar_hsa_circ_224230,RMVar_hsa_circ_272666,RMVar_hsa_circ_224236,RMVar_hsa_circ_224235 76599 RMVar_ID_76599 Human_SNP_ID_170410259 m1A Human chr4 - 1238285 1238285 1238285 AACGGGCCCCTGCACCCGCGGCCCCTGGTGGCATTGCTGGATGGCCGGGACTGCACAGTGGAGAT AACGGGCCCCTGCACCCGCGGCCCCTGGTGGCGTTGCTGGATGGCCGGGACTGCACAGTGGAGAT T C CTBP1 Ensembl:ENSG00000159692 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1238198..1238300 32194978 MeRIP-seq:(Medium) rs751631683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_612738,Human_RBP_ID_4795226,Human_RBP_ID_7264029,Human_RBP_ID_9396873,Human_RBP_ID_15037508,Human_RBP_ID_18017642,Human_RBP_ID_18194982,Human_RBP_ID_22287492,Human_RBP_ID_26349735,Human_RBP_ID_27061873,Human_RBP_ID_27323863 Human_Splice_Rec_537108,Human_Splice_Rec_537124,Human_Splice_Rec_537186,Human_Splice_Rec_537198,Human_Splice_Rec_537212,Human_Splice_Rec_537220,Human_Splice_Rec_537226,Human_Splice_Rec_537228 Human_miRNA_ID_1749507,Human_miRNA_ID_2897999,Human_miRNA_ID_2898000 RMVar_hsa_circ_306179,RMVar_hsa_circ_334775,RMVar_hsa_circ_21874,RMVar_hsa_circ_224234,RMVar_hsa_circ_224231,RMVar_hsa_circ_282062,RMVar_hsa_circ_286412,RMVar_hsa_circ_101054,RMVar_hsa_circ_308822,RMVar_hsa_circ_224230,RMVar_hsa_circ_272666,RMVar_hsa_circ_224236,RMVar_hsa_circ_224235,RMVar_hsa_circ_315197 76600 RMVar_ID_76600 Human_SNP_ID_170411489 m1A Human chr4 + 1241586 1241586 1241586 CATCGAAGGTCCGACCAGAACTCACAGACTCCAGGGAACGCCTCAGAAGTGGACCTCACTGCATC CATCGAAGGTCCGACCAGAACTCACAGACTCCGGGGAACGCCTCAGAAGTGGACCTCACTGCATC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1241584..1248670 32194978 MeRIP-seq:(Medium) rs1410012930 Functional Loss SNV dbSNP153 33..33 33 - - - 76601 RMVar_ID_76601 Human_SNP_ID_170412182 m1A Human chr4 + 1243552 1243552 1243552 ACAGCCCTGGGGTAGGTCTGCCCACCATCTGCACCACCCTGGGGCCACTGTGCACCCACAAAGCG ACAGCCCTGGGGTAGGTCTGCCCACCATCTGCCCCACCCTGGGGCCACTGTGCACCCACAAAGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1243550..1243634 26863196 MeRIP-seq:(Medium) rs920607268 Functional Loss SNV dbSNP153 33..33 33 - - - 76602 RMVar_ID_76602 Human_SNP_ID_170412488 m1A Human chr4 - 1244365 1244365 1244365 GCATCTTGGTGCCCCCTGGGACTTCCTGGAACACCCCCCCCCCAGTGCCCAGAGACCCACTGTGG GCATCTTGGTGCCCCCTGGGACTTCCTGGAACCCCCCCCCCCCAGTGCCCAGAGACCCACTGTGG T G CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1244358..1244654 26863196 MeRIP-seq:(Medium) rs887082034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266866,Human_RBP_ID_5241878,Human_RBP_ID_8236609 RMVar_hsa_circ_101054,RMVar_hsa_circ_224236 76603 RMVar_ID_76603 Human_SNP_ID_170412902 m1A Human chr4 + 1245631 1245630 1245632 ACGGGAGGGCAGGGTGACACGGGCGGCATAGCAGAGTGGCATGGACGGGCAGGGTGACACGGGCG ACGGGAGGGCAGGGTGACACGGGCGGCATAGC__AGTGGCATGGACGGGCAGGGTGACACGGGCG CAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:1245541..1245720 26863196 MeRIP-seq:(Medium) rs1301321730 Functional Loss DEL dbSNP153 33..34 33 - - - 76604 RMVar_ID_76604 Human_SNP_ID_170412903 m1A Human chr4 + 1245631 1245631 1245631 ACGGGAGGGCAGGGTGACACGGGCGGCATAGCAGAGTGGCATGGACGGGCAGGGTGACACGGGCG ACGGGAGGGCAGGGTGACACGGGCGGCATAGCCGAGTGGCATGGACGGGCAGGGTGACACGGGCG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:1245541..1245720 26863196 MeRIP-seq:(Medium) rs1411782002 Functional Loss SNV dbSNP153 33..33 33 - - - 76605 RMVar_ID_76605 Human_SNP_ID_170413609 m1A Human chr4 - 1247629 1247629 1247629 GCTCCTAGCGCGTGGCCTTTGCGCGTCTGTGTACCCGTCTGCAGCTTGGGGCAGGGTTGGGGGAG GCTCCTAGCGCGTGGCCTTTGCGCGTCTGTGTGCCCGTCTGCAGCTTGGGGCAGGGTTGGGGGAG T C CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1247624..1247901 26863196 MeRIP-seq:(Medium) rs190221504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213919,Human_RBP_ID_939504,Human_RBP_ID_1107395,Human_RBP_ID_3749291,Human_RBP_ID_5393950,Human_RBP_ID_8130174,Human_RBP_ID_18464818,Human_RBP_ID_18501234,Human_RBP_ID_22481672,Human_RBP_ID_22702272 RMVar_hsa_circ_101054,RMVar_hsa_circ_224236 76606 RMVar_ID_76606 Human_SNP_ID_170413610 m1A Human chr4 - 1247629 1247629 1247629 GCTCCTAGCGCGTGGCCTTTGCGCGTCTGTGTACCCGTCTGCAGCTTGGGGCAGGGTTGGGGGAG GCTCCTAGCGCGTGGCCTTTGCGCGTCTGTGTCCCCGTCTGCAGCTTGGGGCAGGGTTGGGGGAG T G CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1247624..1247901 26863196 MeRIP-seq:(Medium) rs190221504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213919,Human_RBP_ID_939504,Human_RBP_ID_1107395,Human_RBP_ID_3749291,Human_RBP_ID_5393950,Human_RBP_ID_8130174,Human_RBP_ID_18464818,Human_RBP_ID_18501234,Human_RBP_ID_22481672,Human_RBP_ID_22702272 RMVar_hsa_circ_101054,RMVar_hsa_circ_224236 76607 RMVar_ID_76607 Human_SNP_ID_170413817 m1A Human chr4 - 1247977 1247977 1247977 TCTGGCGGCCTCCAAGGGCGCCGGTGTCTGGAAGCCCGGCCTGGGCCAGATCCCTTTTGCTGTCG TCTGGCGGCCTCCAAGGGCGCCGGTGTCTGGACGCCCGGCCTGGGCCAGATCCCTTTTGCTGTCG T G CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1247968..1248342 26863196 MeRIP-seq:(Medium) rs1219818069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3747809,Human_RBP_ID_4772010 RMVar_hsa_circ_101054,RMVar_hsa_circ_224236 76608 RMVar_ID_76608 Human_SNP_ID_170413891 m1A Human chr4 + 1248134 1248134 1248134 CCGGCCCAGGACGCGGGCGCTGCAAGATGGCGATGGTGGCAAGCCCGGCGCCCGCCCGTGCTCCC CCGGCCCAGGACGCGGGCGCTGCAAGATGGCGCTGGTGGCAAGCCCGGCGCCCGCCCGTGCTCCC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:1248033..1248179 26863196 MeRIP-seq:(Medium) rs1239329701 Functional Loss SNV dbSNP153 33..33 33 - - - 76609 RMVar_ID_76609 Human_SNP_ID_170414372 m1A Human chr4 + 1248967 1248967 1248967 GAGCAAGTGCGAGCTGCCCATCGAGAGGCGCGAGCGGCCGCGGGCCCCGACCACTCCGGCGCGCT GAGCAAGTGCGAGCTGCCCATCGAGAGGCGCGGGCGGCCGCGGGCCCCGACCACTCCGGCGCGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1248669..1248994 32194978 MeRIP-seq:(Medium) rs1411378110 Functional Loss SNV dbSNP153 33..33 33 - - - 76610 RMVar_ID_76610 Human_SNP_ID_170414981 m1A Human chr4 - 1250426 1250415 1250426 TGCAGGGCTGCCCCTCCCCCTACAAGGGCTCCACACGTGTTCCCTCCTTCATGACTCCCACTGGG TGCAGGGCTGCCCCTCCCCCTACAAGGGCTCC___________CTCCTTCATGACTCCCACTGGG GGGAACACGTGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1250375..1250632 26863196 MeRIP-seq:(Medium) rs1293850288 Functional Loss DEL dbSNP153 33..43 33 - - - 76611 RMVar_ID_76611 Human_SNP_ID_170415345 m1A Human chr4 + 1251091 1251091 1251091 TTCCCCATCGTCACTCTCCATGGCCTCCGTCTACACACAGTGTTCGTCTGCACAGCTTGTCAGCG TTCCCCATCGTCACTCTCCATGGCCTCCGTCTGCACACAGTGTTCGTCTGCACAGCTTGTCAGCG A G CTBP1-DT Ensembl:ENSG00000196810 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1251043..1251155 26863196 MeRIP-seq:(Medium) rs1564508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795966,Human_RBP_ID_5102948,Human_RBP_ID_8266138 Human_miRNA_ID_3153296,Human_miRNA_ID_3160651 GWAS_ID_9212,GWAS_ID_9213,GWAS_ID_9214,GWAS_ID_9215,GWAS_ID_9216,GWAS_ID_9217,GWAS_ID_9218,GWAS_ID_9219,GWAS_ID_9220,GWAS_ID_9221,GWAS_ID_9222,GWAS_ID_9223,GWAS_ID_9224,GWAS_ID_9225,GWAS_ID_9226,GWAS_ID_9227,GWAS_ID_9228,GWAS_ID_9229,GWAS_ID_9230 76612 RMVar_ID_76612 Human_SNP_ID_170426011 m1A Human chr4 - 1289948 1289948 1289948 TGAGGGTCGGGTACTCCTGGACCTTCAGGGTCATGGACAACTGAGCCGCCGACTCCTGCACCGCC TGAGGGTCGGGTACTCCTGGACCTTCAGGGTCGTGGACAACTGAGCCGCCGACTCCTGCACCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1289901..1290031 26863196 MeRIP-seq:(Medium) rs1483204341 Functional Loss SNV dbSNP153 33..33 33 - - - 76613 RMVar_ID_76613 Human_SNP_ID_170426014 m1A Human chr4 + 1289950 1289950 1289950 CGGTGCAGGAGTCGGCGGCTCAGTTGTCCATGACCCTGAAGGTCCAGGAGTACCCGACCCTCAAG CGGTGCAGGAGTCGGCGGCTCAGTTGTCCATGTCCCTGAAGGTCCAGGAGTACCCGACCCTCAAG A T MAEA Ensembl:ENSG00000090316 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1289901..1290035 26863196 MeRIP-seq:(Medium) rs1185006660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794808,Human_RBP_ID_19014105,Human_RBP_ID_19122000,Human_RBP_ID_23034775,Human_RBP_ID_26349009 Human_Splice_Rec_537245,Human_Splice_Rec_537263,Human_Splice_Rec_537267,Human_Splice_Rec_537277,Human_Splice_Rec_537287,Human_Splice_Rec_537301,Human_Splice_Rec_537317,Human_Splice_Rec_537323,Human_Splice_Rec_537331,Human_Splice_Rec_537343,Human_Splice_Rec_537345,Human_Splice_Rec_537353 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238 76614 RMVar_ID_76614 Human_SNP_ID_170426027 m1A Human chr4 + 1289981 1289981 1289981 GACCCTGAAGGTCCAGGAGTACCCGACCCTCAAGGTGGGCGCCTGCGCCGCGCAGGCTGAGGGCA GACCCTGAAGGTCCAGGAGTACCCGACCCTCAGGGTGGGCGCCTGCGCCGCGCAGGCTGAGGGCA A G MAEA Ensembl:ENSG00000090316 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1289932..1290023 26863196 MeRIP-seq:(Medium) rs773549747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794808,Human_RBP_ID_19014105,Human_RBP_ID_19122000,Human_RBP_ID_23034775,Human_RBP_ID_26349009 Human_Splice_Rec_537245,Human_Splice_Rec_537263,Human_Splice_Rec_537267,Human_Splice_Rec_537277,Human_Splice_Rec_537287,Human_Splice_Rec_537301,Human_Splice_Rec_537317,Human_Splice_Rec_537323,Human_Splice_Rec_537331,Human_Splice_Rec_537343,Human_Splice_Rec_537345,Human_Splice_Rec_537353 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238 76615 RMVar_ID_76615 Human_SNP_ID_170427827 m1A Human chr4 - 1295834 1295813 1295834 CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGAGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC CGCAGGTGTGGTGGGCACCGGCATGGGTGAGG_____________________GGGCACAGGCGC CCCTCACCCACGCCTGTGCCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1295829..1295912 26863196 MeRIP-seq:(Medium) rs1229761582 Functional Loss DEL dbSNP153 33..53 33 - - - 76616 RMVar_ID_76616 Human_SNP_ID_170427838 m1A Human chr4 - 1295834 1295833 1295834 CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGAGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC CGCAGGTGTGGTGGGCACCGGCATGGGTGAGG_GGGCACAGGCGTGGGTGAGGGGGCACAGGCGC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1295829..1295912 26863196 MeRIP-seq:(Medium) rs1159241637 Functional Loss DEL dbSNP153 33..33 33 - - - 76617 RMVar_ID_76617 Human_SNP_ID_170427839 m1A Human chr4 - 1295834 1295834 1295834 CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGAGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGTGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1295829..1295912 26863196 MeRIP-seq:(Medium) rs1286275509 Functional Loss SNV dbSNP153 33..33 33 - - - 76618 RMVar_ID_76618 Human_SNP_ID_170427840 m1A Human chr4 - 1295834 1295834 1295834 CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGAGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC CGCAGGTGTGGTGGGCACCGGCATGGGTGAGGGGGGCACAGGCGTGGGTGAGGGGGCACAGGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1295829..1295912 26863196 MeRIP-seq:(Medium) rs1286275509 Functional Loss SNV dbSNP153 33..33 33 - - - 76619 RMVar_ID_76619 Human_SNP_ID_170434824 m1A Human chr4 - 1317337 1317337 1317337 GAGTCCGGAGTGTGGGGCCTGCAGATGAGTCCAGAGTGTGGGGCCTGCGGGTGAGTCTGGAGTGT GAGTCCGGAGTGTGGGGCCTGCAGATGAGTCCGGAGTGTGGGGCCTGCGGGTGAGTCTGGAGTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1317335..1317400 26863196 MeRIP-seq:(Medium) rs1157240854 Functional Loss SNV dbSNP153 33..33 33 - - - 76620 RMVar_ID_76620 Human_SNP_ID_170437337 m1A Human chr4 + 1324338 1324338 1324338 ATGAAGTTGAGATTGGTTTGGATGAAGTTGAGATTGGATGCCTGGTGGACGAGTGTGTCTGGTGT ATGAAGTTGAGATTGGTTTGGATGAAGTTGAGGTTGGATGCCTGGTGGACGAGTGTGTCTGGTGT A G MAEA Ensembl:ENSG00000090316 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:1324288..1324527 26863196 MeRIP-seq:(Medium) rs1211618301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5654951,Human_RBP_ID_24035563 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238,RMVar_hsa_circ_297834,RMVar_hsa_circ_366989,RMVar_hsa_circ_73620 76621 RMVar_ID_76621 Human_SNP_ID_170439093 m1A Human chr4 + 1329625 1329625 1329625 GGGGCCGTCTTGGGAGTGGTTCTCCAGGTGCCAGGGCCTGGTCAGGGAAGTCCGGCCTCAGCTCA GGGGCCGTCTTGGGAGTGGTTCTCCAGGTGCCCGGGCCTGGTCAGGGAAGTCCGGCCTCAGCTCA A C MAEA Ensembl:ENSG00000090316 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:1329621..1329777;chr4:1329619..1329729 26863196 MeRIP-seq:(Medium) rs1260583440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837158,Human_RBP_ID_3747192,Human_RBP_ID_8129706,Human_RBP_ID_18424692,Human_RBP_ID_18500675,Human_RBP_ID_22418463,Human_RBP_ID_22745743,Human_RBP_ID_24430577 RMVar_hsa_circ_38528,RMVar_hsa_circ_84625,RMVar_hsa_circ_224238,RMVar_hsa_circ_366989 76622 RMVar_ID_76622 Human_SNP_ID_170442099 m1A Human chr4 - 1337381 1337381 1337381 GGACAGAGTCACAGGCAGACAGAGTCGGTCACAGGTGGGACAGAGTCAGTCACAGGCGGGACAGA GGACAGAGTCACAGGCAGACAGAGTCGGTCACGGGTGGGACAGAGTCAGTCACAGGCGGGACAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1337378..1337449 26863196 MeRIP-seq:(Medium) rs551250625 Functional Loss SNV dbSNP153 33..33 33 - - - 76623 RMVar_ID_76623 Human_SNP_ID_170442199 m1A Human chr4 - 1337718 1337716 1337718 TCACAGGTGAGACAGTCACAGGGCAGGGGCAGAGTCAGTCACAGGCGAGGACAGAGTCACAGGCG TCACAGGTGAGACAGTCACAGGGCAGGGGCAG__TCAGTCACAGGCGAGGACAGAGTCACAGGCG ACT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1337716..1337836 26863196 MeRIP-seq:(Medium) rs1450534800 Functional Loss DEL dbSNP153 33..34 33 - - - 76624 RMVar_ID_76624 Human_SNP_ID_170445455 m1A Human chr4 - 1347432 1347419 1347432 GGACCGCGGGGTCGCTCTCGCACAGCGGCTGCACCGGGCGGGCGCGCCGGCTTCGACGGTGCTCG GGACCGCGGGGTCGCTCTCGCACAGCGGCTGC_____________GCCGGCTTCGACGGTGCTCG CGCGCCCGCCCGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:1347243..1347501;chr4:1347243..1347554;chr4:1347248..1347524 26863196 MeRIP-seq:(Medium) rs557259513 Functional Loss DEL dbSNP153 33..45 33 - - - 76625 RMVar_ID_76625 Human_SNP_ID_170445720 m1A Human chr4 - 1348093 1348093 1348093 GCTCTTCTACCAACTTCGAAAGTTTCTGATCCATATCTAGAAATAAGTAAGGCAGAGATGCTATA GCTCTTCTACCAACTTCGAAAGTTTCTGATCCGTATCTAGAAATAAGTAAGGCAGAGATGCTATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1348082..1348171 26863196 MeRIP-seq:(Medium) rs779101623 Functional Loss SNV dbSNP153 33..33 33 - - - 76626 RMVar_ID_76626 Human_SNP_ID_170445721 m1A Human chr4 - 1348093 1348093 1348093 GCTCTTCTACCAACTTCGAAAGTTTCTGATCCATATCTAGAAATAAGTAAGGCAGAGATGCTATA GCTCTTCTACCAACTTCGAAAGTTTCTGATCCCTATCTAGAAATAAGTAAGGCAGAGATGCTATA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1348082..1348171 26863196 MeRIP-seq:(Medium) rs779101623 Functional Loss SNV dbSNP153 33..33 33 - - - 76627 RMVar_ID_76627 Human_SNP_ID_170446483 m1A Human chr4 - 1349797 1349797 1349797 TAGCCCAAGGCAAGCTTCTTGTAGGCCTCCCCAAACTTCTCATTCCACCCTTCCACGGCCCGGGT TAGCCCAAGGCAAGCTTCTTGTAGGCCTCCCCTAACTTCTCATTCCACCCTTCCACGGCCCGGGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1349749..1349850 32194978 MeRIP-seq:(Medium) rs1380308959 Functional Loss SNV dbSNP153 33..33 33 - - - 76628 RMVar_ID_76628 Human_SNP_ID_170448096 m1A Human chr4 + 1353930 1353930 1353930 GGCACTGCAGCCTGGGTGGGTGAGGATTGCAGAGACATAGCCGCCCCCGCCCCCCAGCCCCAGCT GGCACTGCAGCCTGGGTGGGTGAGGATTGCAGTGACATAGCCGCCCCCGCCCCCCAGCCCCAGCT A T UVSSA Ensembl:ENSG00000163945 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1353730..1353977 26863196 MeRIP-seq:(Medium) rs1435756933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266710 RMVar_hsa_circ_24148,RMVar_hsa_circ_92661,RMVar_hsa_circ_324613,RMVar_hsa_circ_119583,RMVar_hsa_circ_353663,RMVar_hsa_circ_224243,RMVar_hsa_circ_335689,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244,RMVar_hsa_circ_31335 76629 RMVar_ID_76629 Human_SNP_ID_170448299 m1A Human chr4 + 1354402 1354402 1354402 GGCGCCATCCTGTGGCGTGGGCTGTGGAGGGGAAGGTTCTGTGCCCGGCGTGTGGGGGCGGTGAG GGCGCCATCCTGTGGCGTGGGCTGTGGAGGGGTAGGTTCTGTGCCCGGCGTGTGGGGGCGGTGAG A T UVSSA Ensembl:ENSG00000163945 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:1354263..1354501;chr4:1354200..1354563 26863196 MeRIP-seq:(Medium) rs573868280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266711,Human_RBP_ID_786219,Human_RBP_ID_939513,Human_RBP_ID_1069277,Human_RBP_ID_3747208,Human_RBP_ID_3966031,Human_RBP_ID_5210865,Human_RBP_ID_5241899,Human_RBP_ID_5326227,Human_RBP_ID_5393955,Human_RBP_ID_8130226,Human_RBP_ID_8211496,Human_RBP_ID_8236615,Human_RBP_ID_9334536,Human_RBP_ID_9435727,Human_RBP_ID_18413451,Human_RBP_ID_19121353,Human_RBP_ID_21988501,Human_RBP_ID_22418542,Human_RBP_ID_22457635,Human_RBP_ID_22481209,Human_RBP_ID_22745537,Human_RBP_ID_23213939,Human_RBP_ID_26349032,Human_RBP_ID_26791204 RMVar_hsa_circ_24148,RMVar_hsa_circ_92661,RMVar_hsa_circ_324613,RMVar_hsa_circ_119583,RMVar_hsa_circ_353663,RMVar_hsa_circ_224243,RMVar_hsa_circ_335689,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244,RMVar_hsa_circ_31335 76630 RMVar_ID_76630 Human_SNP_ID_170448487 m1A Human chr4 + 1354801 1354801 1354801 TGCTCTCATCCACGCCGCCCGCGACACACTCAAGCTCATCCGGAACAAGTTCCTGCCGGCTGTGT TGCTCTCATCCACGCCGCCCGCGACACACTCAGGCTCATCCGGAACAAGTTCCTGCCGGCTGTGT A G UVSSA Ensembl:ENSG00000163945 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1353103..1355104 32194978 MeRIP-seq:(Medium) rs1325045818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9396895 Human_Splice_Rec_537434,Human_Splice_Rec_537435,Human_Splice_Rec_537456,Human_Splice_Rec_537457,Human_Splice_Rec_537480,Human_Splice_Rec_537481,Human_Splice_Rec_537497 RMVar_hsa_circ_24148,RMVar_hsa_circ_92661,RMVar_hsa_circ_324613,RMVar_hsa_circ_119583,RMVar_hsa_circ_353663,RMVar_hsa_circ_224243,RMVar_hsa_circ_335689,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244,RMVar_hsa_circ_31335 76631 RMVar_ID_76631 Human_SNP_ID_170448758 m1A Human chr4 - 1355247 1355247 1355247 GGGACCCCTTCCCGCTCGCCGCCTGCCCACTCACCCTGCGCCTTTCCCCTCCCTCAGGCTCGATG GGGACCCCTTCCCGCTCGCCGCCTGCCCACTCCCCCTGCGCCTTTCCCCTCCCTCAGGCTCGATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1355221..1355292 26863196 MeRIP-seq:(Medium) rs1489424360 Functional Loss SNV dbSNP153 33..33 33 - - - 76632 RMVar_ID_76632 Human_SNP_ID_170452498 m1A Human chr4 - 1366416 1366416 1366416 CGGGACCCACTGCTCACCATACTCAGGCCGCAAGTGGTCGGGGATGTGTGGCTCATACCCCTCCT CGGGACCCACTGCTCACCATACTCAGGCCGCAGGTGGTCGGGGATGTGTGGCTCATACCCCTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1366283..1374959 32194978 MeRIP-seq:(Medium) rs772424340 Functional Loss SNV dbSNP153 33..33 33 - - - 76633 RMVar_ID_76633 Human_SNP_ID_170457512 m1A Human chr4 + 1380078 1380078 1380078 GGTCTGACTCCCAGCACCGCTTCTGGAAGCCCAGCGAGGTGGAGGAGGAAGTGGTCAATGCCGAC GGTCTGACTCCCAGCACCGCTTCTGGAAGCCCGGCGAGGTGGAGGAGGAAGTGGTCAATGCCGAC A G UVSSA Ensembl:ENSG00000163945 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1375391..1380654 32194978 MeRIP-seq:(Medium) rs748676865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26349036 Human_Splice_Rec_537444,Human_Splice_Rec_537466,Human_Splice_Rec_537490,Human_Splice_Rec_537504,Human_Splice_Rec_537514,Human_Splice_Rec_537522 RMVar_hsa_circ_24148,RMVar_hsa_circ_92661,RMVar_hsa_circ_353663,RMVar_hsa_circ_224244,RMVar_hsa_circ_43325,RMVar_hsa_circ_26832,RMVar_hsa_circ_70729 76634 RMVar_ID_76634 Human_SNP_ID_170457952 m1A Human chr4 - 1380990 1380990 1380990 TGCCTCCCACGGTGACCGCCTTGCCCAGACCTACCCGGGCGCTCCTGCTTCTGCAGCTGCCGCCG TGCCTCCCACGGTGACCGCCTTGCCCAGACCTCCCCGGGCGCTCCTGCTTCTGCAGCTGCCGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:1380952..1381023;chr4:1380953..1381031 26863196 MeRIP-seq:(Medium) rs767271099 Functional Loss SNV dbSNP153 33..33 33 - - - 76635 RMVar_ID_76635 Human_SNP_ID_170459283 m1A Human chr4 + 1384911 1384910 1384911 GTGGTACATCCACAGCCTTGCTTGGGTGGGGCAGGGGCGCTGGTGGGGGCTGTGGAGAGGCTGCC GTGGTACATCCACAGCCTTGCTTGGGTGGGGC_GGGGCGCTGGTGGGGGCTGTGGAGAGGCTGCC CA C UVSSA Ensembl:ENSG00000163945 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1384910..1385060 32194978 MeRIP-seq:(Medium) rs970464156 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26791081 76636 RMVar_ID_76636 Human_SNP_ID_170459640 m1A Human chr4 + 1385921 1385921 1385921 GGCAGCCATGAACCGGATGGACCAGAAGAAGCACGAGAAGTTTTCAAACCAGTTTAACTACGCAC GGCAGCCATGAACCGGATGGACCAGAAGAAGCGCGAGAAGTTTTCAAACCAGTTTAACTACGCAC A G UVSSA Ensembl:ENSG00000163945 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1385861..1385937 26863196 MeRIP-seq:(Medium) rs1187804842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15050817 Human_Splice_Rec_537450,Human_Splice_Rec_537472,Human_Splice_Rec_537496,Human_Splice_Rec_537510,Human_Splice_Rec_537520,Human_Splice_Rec_537530 Human_miRNA_ID_1799259 76637 RMVar_ID_76637 Human_SNP_ID_170497961 m1A Human chr4 - 1515448 1515448 1515448 TCATGACCATCATCACCATCACCATCATCACCACCATCACAACCATCACCATCACAATCATCACC TCATGACCATCATCACCATCACCATCATCACCCCCATCACAACCATCACCATCACAATCATCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:1515414..1515498;chr4:1515391..1515487 26863196 MeRIP-seq:(Medium) rs1375836326 Functional Loss SNV dbSNP153 33..33 33 - - - 76638 RMVar_ID_76638 Human_SNP_ID_170512586 m1A Human chr4 - 1561016 1561016 1561016 CCCCGTACCTAGTGAGGGGTGCCCAGCCTTCCAGGCCCCGCCATGGGCCCCGCAGCTTCTCCCGG CCCCGTACCTAGTGAGGGGTGCCCAGCCTTCCGGGCCCCGCCATGGGCCCCGCAGCTTCTCCCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1561005..1561137 26863196 MeRIP-seq:(Medium) rs530456272 Functional Loss SNV dbSNP153 33..33 33 - - - 76639 RMVar_ID_76639 Human_SNP_ID_170541004 m1A Human chr4 - 1652154 1652154 1652154 ATGGTGTGTGTGGCGTGTGGGGTGTGTGTGTGACGTGTGGTGTGTGTGGTGTATGAGGTGTGTGT ATGGTGTGTGTGGCGTGTGGGGTGTGTGTGTGGCGTGTGGTGTGTGTGGTGTATGAGGTGTGTGT T C FAM53A Ensembl:ENSG00000174137 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1651928..1652938 26863196 MeRIP-seq:(Medium) rs1485290609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5655253 76640 RMVar_ID_76640 Human_SNP_ID_170541066 m1A Human chr4 + 1652236 1652236 1652236 CACATGCCACACACACCACACACACTAGTCGCACACACACCACACACACCACACGCCAGACACCG CACATGCCACACACACCACACACACTAGTCGCTCACACACCACACACACCACACGCCAGACACCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1651971..1653094 26863196 MeRIP-seq:(Medium) rs1326904252 Functional Loss SNV dbSNP153 33..33 33 - - - 76641 RMVar_ID_76641 Human_SNP_ID_170541308 m1A Human chr4 + 1652744 1652744 1652744 CACCACACACACTACCAGAGACCACACACTGCACACACACACCACACACAGACTACACACCACAC CACCACACACACTACCAGAGACCACACACTGCGCACACACACCACACACAGACTACACACCACAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1651938..1653023 26863196 MeRIP-seq:(Medium) rs13131486 Functional Loss SNV dbSNP153 33..33 33 - - - 76642 RMVar_ID_76642 Human_SNP_ID_170541357 m1A Human chr4 + 1652858 1652843 1652859 CACCACACACCACACGCTACACACCACACAGCACACACACCACACACCAAACACCACACATACCA CACCACACACCACACGCT________________ACACACCACACACCAAACACCACACATACCA TACACACCACACAGCAC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:1652647..1652896 26863196 MeRIP-seq:(Medium) rs1430395574 Functional Loss DEL dbSNP153 19..34 33 - - - 76643 RMVar_ID_76643 Human_SNP_ID_170547041 m1A Human chr4 + 1671385 1671385 1671385 CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCACCAGCTCACAGCCACGGCCCGGACTCACCTCT CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCCCCAGCTCACAGCCACGGCCCGGACTCACCTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:1670835..1671435;chr4:1670890..1671458 26863196 MeRIP-seq:(Medium) rs28458319 Functional Loss SNV dbSNP153 33..33 33 - - - 76644 RMVar_ID_76644 Human_SNP_ID_170547042 m1A Human chr4 + 1671385 1671385 1671385 CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCACCAGCTCACAGCCACGGCCCGGACTCACCTCT CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCGCCAGCTCACAGCCACGGCCCGGACTCACCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:1670835..1671435;chr4:1670890..1671458 26863196 MeRIP-seq:(Medium) rs28458319 Functional Loss SNV dbSNP153 33..33 33 - - - 76645 RMVar_ID_76645 Human_SNP_ID_170555763 m1A Human chr4 - 1699615 1699615 1699615 AAGTGTCCTAATGAGGAGACAGAAGCAGATCAACTATGGGAAGAACACAATTGCCTACGATCGTT AAGTGTCCTAATGAGGAGACAGAAGCAGATCAGCTATGGGAAGAACACAATTGCCTACGATCGTT T C SLBP Ensembl:ENSG00000163950 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1699551..1699625 32194978 MeRIP-seq:(Medium) rs1295807412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71922,Human_RBP_ID_1035702,Human_RBP_ID_1636263,Human_RBP_ID_1974571,Human_RBP_ID_7348818,Human_RBP_ID_9396010,Human_RBP_ID_15091908,Human_RBP_ID_17671444,Human_RBP_ID_26349039,Human_RBP_ID_27063876,Human_RBP_ID_27725485 Human_Splice_Rec_537588,Human_Splice_Rec_537589,Human_Splice_Rec_537600,Human_Splice_Rec_537601,Human_Splice_Rec_537614,Human_Splice_Rec_537615,Human_Splice_Rec_537624,Human_Splice_Rec_537625,Human_Splice_Rec_537636,Human_Splice_Rec_537637,Human_Splice_Rec_537648,Human_Splice_Rec_537649 RMVar_hsa_circ_118126,RMVar_hsa_circ_298158,RMVar_hsa_circ_224248,RMVar_hsa_circ_93942,RMVar_hsa_circ_224247,RMVar_hsa_circ_322608,RMVar_hsa_circ_224251,RMVar_hsa_circ_224252,RMVar_hsa_circ_280609,RMVar_hsa_circ_301597,RMVar_hsa_circ_326624,RMVar_hsa_circ_224253 76646 RMVar_ID_76646 Human_SNP_ID_170557014 m1A Human chr4 - 1703676 1703676 1703676 TATTGCAGCTTTACCACTCCTGAAGGCCCTAAACCCCGTTCCAGATGCTCTGACTGGGCAAGTGC TATTGCAGCTTTACCACTCCTGAAGGCCCTAAGCCCCGTTCCAGATGCTCTGACTGGGCAAGTGC T C SLBP Ensembl:ENSG00000163950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:1703626..1703675 26863196 MeRIP-seq:(Medium) rs140082881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249131,Human_RBP_ID_616379,Human_RBP_ID_7286706,Human_RBP_ID_17294061,Human_RBP_ID_17523149,Human_RBP_ID_18021763,Human_RBP_ID_27507065 Human_Splice_Rec_537584,Human_Splice_Rec_537585,Human_Splice_Rec_537596,Human_Splice_Rec_537597,Human_Splice_Rec_537610,Human_Splice_Rec_537611,Human_Splice_Rec_537644,Human_Splice_Rec_537645 Human_miRNA_ID_2950213 RMVar_hsa_circ_298158,RMVar_hsa_circ_224248,RMVar_hsa_circ_93942,RMVar_hsa_circ_224251,RMVar_hsa_circ_224252,RMVar_hsa_circ_280609,RMVar_hsa_circ_375045,RMVar_hsa_circ_64168,RMVar_hsa_circ_224254 76647 RMVar_ID_76647 Human_SNP_ID_170559637 m1A Human chr4 + 1711853 1711853 1711853 CGCGGCCTCGTCAAGGGCCCCACCGCGCCCCGACCCCCGGGTCCCGCGCCCACCTCTCGGGTCTG CGCGGCCTCGTCAAGGGCCCCACCGCGCCCCGTCCCCCGGGTCCCGCGCCCACCTCTCGGGTCTG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:1711851..1712200;chr4:1711851..1711875;chr4:1711851..1712000 26863196 MeRIP-seq:(Medium) rs1293850978 Functional Loss SNV dbSNP153 33..33 33 - - - 76648 RMVar_ID_76648 Human_SNP_ID_170559832 m1A Human chr4 + 1712222 1712216 1712222 GCAGCACGGGCCGGGCGCGCAGCGCAGGGCCGAGGCTGAGGCGGCGGCGGCGCGGGCAGAGAGCG GCAGCACGGGCCGGGCGCGCAGCGCAG______GGCTGAGGCGGCGGCGGCGCGGGCAGAGAGCG GGGCCGA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:1712126..1712325 26863410 MeRIP-seq:(Medium) rs1205718406 Functional Loss DEL dbSNP153 28..33 33 - - - 76649 RMVar_ID_76649 Human_SNP_ID_170560216 m1A Human chr4 + 1712968 1712968 1712968 TTTTGGAGTAACCTTTTAGGTCGCAACAGTTGACAACTACACTGAGTCTTTCCGGTCCCACTGCC TTTTGGAGTAACCTTTTAGGTCGCAACAGTTGCCAACTACACTGAGTCTTTCCGGTCCCACTGCC A C TACC3,AC016773.2 Ensembl:ENSG00000013810,Ensembl:ENSG00000270195 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1712917..1712983 26863196 MeRIP-seq:(Medium) rs78596127 Functional Loss SNV dbSNP153 33..33 33 - - - 76650 RMVar_ID_76650 Human_SNP_ID_170561915 m1A Human chr4 + 1718477 1718477 1718477 GGCCAGGGTGCGCGCCAGTGGGTGGCAGGCCCACCGGTCACGGGACCAGTAGTAGATCAGGATGC GGCCAGGGTGCGCGCCAGTGGGTGGCAGGCCCTCCGGTCACGGGACCAGTAGTAGATCAGGATGC A T TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1718323..1718561 26863196 MeRIP-seq:(Medium) rs909573653 Functional Loss SNV dbSNP153 33..33 33 - - - 76651 RMVar_ID_76651 Human_SNP_ID_170561921 m1A Human chr4 + 1718489 1718489 1718489 CGCCAGTGGGTGGCAGGCCCACCGGTCACGGGACCAGTAGTAGATCAGGATGCAGGCGATGGAGG CGCCAGTGGGTGGCAGGCCCACCGGTCACGGGGCCAGTAGTAGATCAGGATGCAGGCGATGGAGG A G TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1718439..1718554 26863196 MeRIP-seq:(Medium) rs542420061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15094577 76652 RMVar_ID_76652 Human_SNP_ID_170562688 m1A Human chr4 - 1720683 1720683 1720683 GGGCAGCGAGGACGCCGCCTTCGTGCCCTTCCACTTGCGCCGCACGGCCGCCACGCTGTTGTGCC GGGCAGCGAGGACGCCGCCTTCGTGCCCTTCCCCTTGCGCCGCACGGCCGCCACGCTGTTGTGCC T G TMEM129 Ensembl:ENSG00000168936 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1720581..1720736 26863196 MeRIP-seq:(Medium) rs1455091307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4797974,Human_RBP_ID_26514259 Human_Splice_Rec_537935,Human_Splice_Rec_537941,Human_Splice_Rec_537945,Human_Splice_Rec_537957 76653 RMVar_ID_76653 Human_SNP_ID_170562827 m1A Human chr4 - 1720959 1720928 1720959 GCGGGCGGCCGGGCGGCGGGACTCCATGTCCTAGAGTGCCCCGCGGGCGGCCGGGCGGCGGCCGC GCGGGCGGCCGGGCGGCGGGACTCCATGTCCT_______________________________GC CGGCCGCCGCCCGGCCGCCCGCGGGGCACTCT C TMEM129 Ensembl:ENSG00000168936 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:1720858..1720959 26863410 MeRIP-seq:(Medium) rs1380032455 Functional Loss DEL dbSNP153 33..63 33 - - - Human_RBP_ID_4777736 76654 RMVar_ID_76654 Human_SNP_ID_170562917 m1A Human chr4 - 1721106 1721106 1721106 CTGCATCTCCCAGAGCGCCCCGCGAGCGGCCGAGCGGCGGGACTCCATGCCCTAGAGTGCCCCGC CTGCATCTCCCAGAGCGCCCCGCGAGCGGCCGGGCGGCGGGACTCCATGCCCTAGAGTGCCCCGC T C TMEM129 Ensembl:ENSG00000168936 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1721058..1721159 32194978 MeRIP-seq:(Medium) rs1430619243 Functional Loss SNV dbSNP153 33..33 33 - - - 76655 RMVar_ID_76655 Human_SNP_ID_170563131 m1A Human chr4 - 1721552 1721552 1721552 TCCGCGTCTGCTCCACGCCGGGGGCCAAGCCTAGCTGCTACCGCCGTCGCGCTTCTAGCCCTTGA TCCGCGTCTGCTCCACGCCGGGGGCCAAGCCTGGCTGCTACCGCCGTCGCGCTTCTAGCCCTTGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:1721501..1721676;chr4:1721501..1721720;chr4:1721501..1721682 26863196 MeRIP-seq:(Medium) rs3134865 Functional Loss SNV dbSNP153 33..33 33 - - - 76656 RMVar_ID_76656 Human_SNP_ID_170563135 m1A Human chr4 - 1721558 1721558 1721558 GAGGGGTCCGCGTCTGCTCCACGCCGGGGGCCAAGCCTAGCTGCTACCGCCGTCGCGCTTCTAGC GAGGGGTCCGCGTCTGCTCCACGCCGGGGGCCGAGCCTAGCTGCTACCGCCGTCGCGCTTCTAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1721501..1721670 26863196 MeRIP-seq:(Medium) rs1415691294 Functional Loss SNV dbSNP153 33..33 33 - - - 76657 RMVar_ID_76657 Human_SNP_ID_170563773 m1A Human chr4 + 1723404 1723403 1723405 TGTGGTAGTGTTGCCCTCACACTGACACAAACATGTTCTGCTTTTCCAGAATGAGTCTGCAGGTC TGTGGTAGTGTTGCCCTCACACTGACACAAAC__GTTCTGCTTTTCCAGAATGAGTCTGCAGGTC CAT C TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:1723401..1723500;chr4:1723401..1723475 26863196 MeRIP-seq:(Medium) rs1199825922 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22745541,Human_RBP_ID_25791417 76658 RMVar_ID_76658 Human_SNP_ID_170565277 m1A Human chr4 - 1727999 1727998 1728000 GACTCTGTCCTGCAAGGGTCTTCTAGGGTCTCAGAGGCGGGTGTCACTCTTCTGTCTAAGGAATA GACTCTGTCCTGCAAGGGTCTTCTAGGGTCT__GAGGCGGGTGTCACTCTTCTGTCTAAGGAATA CTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1727951..1728135 26863196 MeRIP-seq:(Medium) rs1195479184 Functional Loss DEL dbSNP153 32..33 33 - - - 76659 RMVar_ID_76659 Human_SNP_ID_170565555 m1A Human chr4 + 1728527 1728527 1728527 CCTCCCTTGAGGAAAGCAGCAGTGAGGCAGCAAAAGGCCCCGCAGGAGGTGGAGGAGGACGACGG CCTCCCTTGAGGAAAGCAGCAGTGAGGCAGCAGAAGGCCCCGCAGGAGGTGGAGGAGGACGACGG A G TACC3 Ensembl:ENSG00000013810 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1728476..1728653 26863196 MeRIP-seq:(Medium) rs798758 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_940496,Human_RBP_ID_4777808,Human_RBP_ID_9396023,Human_RBP_ID_26349767 GWAS_ID_9231 RMVar_hsa_circ_368001,RMVar_hsa_circ_115555,RMVar_hsa_circ_4103,RMVar_hsa_circ_105378,RMVar_hsa_circ_224257,RMVar_hsa_circ_224258,RMVar_hsa_circ_337625,RMVar_hsa_circ_224259,RMVar_hsa_circ_9173 76660 RMVar_ID_76660 Human_SNP_ID_170565569 m1A Human chr4 - 1728544 1728544 1728544 CTCCTGCTCCGCTCCTACCGTCGTCCTCCTCCACCTCCTGCGGGGCCTTTTGCTGCCTCACTGCT CTCCTGCTCCGCTCCTACCGTCGTCCTCCTCCTCCTCCTGCGGGGCCTTTTGCTGCCTCACTGCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1728495..1728618 26863196 MeRIP-seq:(Medium) rs1560300717 Functional Loss SNV dbSNP153 33..33 33 - - - 76661 RMVar_ID_76661 Human_SNP_ID_170567796 m1A Human chr4 + 1735255 1735255 1735255 TTAGGGCCCTGGTGAGGGGCGATGGCGGCGGCATGATTCACTCCTCTCAGTTCTAGGCACGGGCG TTAGGGCCCTGGTGAGGGGCGATGGCGGCGGCCTGATTCACTCCTCTCAGTTCTAGGCACGGGCG A C TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1735251..1735350 26863196 MeRIP-seq:(Medium) rs1560312329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15095088,Human_RBP_ID_22825704 Human_Splice_Rec_537671,Human_Splice_Rec_537701,Human_Splice_Rec_537729,Human_Splice_Rec_537743,Human_Splice_Rec_537761,Human_Splice_Rec_537793,Human_Splice_Rec_537829,Human_Splice_Rec_537859,Human_Splice_Rec_537883,Human_Splice_Rec_537893,Human_Splice_Rec_537901,Human_Splice_Rec_537923 RMVar_hsa_circ_115555,RMVar_hsa_circ_4103,RMVar_hsa_circ_105378,RMVar_hsa_circ_224258,RMVar_hsa_circ_224259,RMVar_hsa_circ_224261,RMVar_hsa_circ_335827,RMVar_hsa_circ_337119,RMVar_hsa_circ_292248,RMVar_hsa_circ_224262,RMVar_hsa_circ_87626,RMVar_hsa_circ_224263 76662 RMVar_ID_76662 Human_SNP_ID_170568905 m1A Human chr4 + 1738144 1738144 1738144 CCGTGCCTTGTCTCCCTCCATCCTCACTGTACATGCCAGGCTTCAGCCTGTTCTAACTCCGGGCC CCGTGCCTTGTCTCCCTCCATCCTCACTGTACCTGCCAGGCTTCAGCCTGTTCTAACTCCGGGCC A C TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1738140..1738340 32194978 MeRIP-seq:(Medium) rs1182110062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160060,Human_RBP_ID_1636412,Human_RBP_ID_15095132,Human_RBP_ID_17089713,Human_RBP_ID_22678974 RMVar_hsa_circ_35611,RMVar_hsa_circ_105378,RMVar_hsa_circ_224259,RMVar_hsa_circ_335827,RMVar_hsa_circ_97820,RMVar_hsa_circ_116244,RMVar_hsa_circ_224264,RMVar_hsa_circ_97732,RMVar_hsa_circ_224268,RMVar_hsa_circ_224270 76663 RMVar_ID_76663 Human_SNP_ID_170568961 m1A Human chr4 + 1738316 1738316 1738316 GTTCCGGAGGCCGGCTGGCAGGGCTGGGTTCAAGCCCCAACATCCACACCAGTGTTGTTCACAGT GTTCCGGAGGCCGGCTGGCAGGGCTGGGTTCAGGCCCCAACATCCACACCAGTGTTGTTCACAGT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs76855141 Functional Loss SNV dbSNP153 33..33 33 - - - 76664 RMVar_ID_76664 Human_SNP_ID_170569429 m1A Human chr4 - 1739769 1739769 1739769 GACAGGAGACGGGGCCTCCTTACCCCAGTTCCAGGTTCTTCCCGTGGAGCTCCTCACACCTGCTC GACAGGAGACGGGGCCTCCTTACCCCAGTTCCTGGTTCTTCCCGTGGAGCTCCTCACACCTGCTC T A lnc-TMEM129-1 RNACentral:URS00008C1A94 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1739657..1739806 26863196 MeRIP-seq:(Medium) rs1036954975 Functional Loss SNV dbSNP153 33..33 33 - - - 76665 RMVar_ID_76665 Human_SNP_ID_170570832 m1A Human chr4 + 1743800 1743800 1743800 CTCCCGGACAGACGCTGTTGGGAATTTTCCACAGCAGAGAAACACAGTGCTGTGGGTTTAAGGGA CTCCCGGACAGACGCTGTTGGGAATTTTCCACTGCAGAGAAACACAGTGCTGTGGGTTTAAGGGA A T TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1743797..1744044 26863196 MeRIP-seq:(Medium) rs1248006763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1636549 76666 RMVar_ID_76666 Human_SNP_ID_170570833 m1A Human chr4 + 1743809 1743808 1743810 AGACGCTGTTGGGAATTTTCCACAGCAGAGAAACACAGTGCTGTGGGTTTAAGGGAGGCGTGACC AGACGCTGTTGGGAATTTTCCACAGCAGAGAA__ACAGTGCTGTGGGTTTAAGGGAGGCGTGACC AAC A TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1743805..1744039 26863196 MeRIP-seq:(Medium) rs1239906897 Functional Loss DEL dbSNP153 33..34 33 - - - 76667 RMVar_ID_76667 Human_SNP_ID_170570843 m1A Human chr4 + 1743847 1743847 1743847 TGCTGTGGGTTTAAGGGAGGCGTGACCTCCGCAGGACATCAGGGGCTGCATGCTGGGTAGGGGCT TGCTGTGGGTTTAAGGGAGGCGTGACCTCCGCCGGACATCAGGGGCTGCATGCTGGGTAGGGGCT A C TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1743843..1743948 26863196 MeRIP-seq:(Medium) rs545709598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15097475 76668 RMVar_ID_76668 Human_SNP_ID_170571259 m1A Human chr4 + 1744917 1744917 1744917 GCCCTTGGGCCTGCTGCTCCCTCCAAGCAGGGAGAAGCCCCGCAACTCATCTTCCTCCTCCAGAC GCCCTTGGGCCTGCTGCTCCCTCCAAGCAGGGTGAAGCCCCGCAACTCATCTTCCTCCTCCAGAC A T TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1744914..1745050 26863196 MeRIP-seq:(Medium) rs767233198 Functional Loss SNV dbSNP153 33..33 33 - - - 76669 RMVar_ID_76669 Human_SNP_ID_170576702 m1A Human chr4 + 1761343 1761343 1761343 ACACTGCCCATGCAACCCGGTGCGCCTTGTCCACCCTGTCCGCCCTGCCTGCCCTGCCTGCCCCG ACACTGCCCATGCAACCCGGTGCGCCTTGTCCCCCCTGTCCGCCCTGCCTGCCCTGCCTGCCCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1761180..1761361 26863196 MeRIP-seq:(Medium) rs944195080 Functional Loss SNV dbSNP153 33..33 33 - - - 76670 RMVar_ID_76670 Human_SNP_ID_170579360 m1A Human chr4 + 1767824 1767824 1767824 CCAGCAGCGGCCCGGAGCTGCCCTTTGTGCAGAGCTGGGGCGGCCCGTACCGTCGTGCCCTTCGG CCAGCAGCGGCCCGGAGCTGCCCTTTGTGCAGGGCTGGGGCGGCCCGTACCGTCGTGCCCTTCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1767775..1767879 26863196 MeRIP-seq:(Medium) rs543504821 Functional Loss SNV dbSNP153 33..33 33 - - - 76671 RMVar_ID_76671 Human_SNP_ID_170579444 m1A Human chr4 - 1767979 1767979 1767979 GGCTGCCGGGAGGAGGCGGTGCTGGGGTTGCGAAGAAGGGCTGGAAGCCGGGGCCTGGGGTGGGG GGCTGCCGGGAGGAGGCGGTGCTGGGGTTGCGTAGAAGGGCTGGAAGCCGGGGCCTGGGGTGGGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1767976..1768108 26863196 MeRIP-seq:(Medium) rs1437972018 Functional Loss SNV dbSNP153 33..33 33 - - - 76672 RMVar_ID_76672 Human_SNP_ID_170581252 m1A Human chr4 + 1773888 1773888 1773888 AGCTCTGGCCTGGGACGGTGGCTCTGGGCTCTAGGGCTCCTAAACTCACTGCTGGGCTTGTGGCC AGCTCTGGCCTGGGACGGTGGCTCTGGGCTCTGGGGCTCCTAAACTCACTGCTGGGCTTGTGGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1773880..1773999 26863196 MeRIP-seq:(Medium) rs1189457496 Functional Loss SNV dbSNP153 33..33 33 - - - 76673 RMVar_ID_76673 Human_SNP_ID_170582345 m1A Human chr4 - 1777526 1777526 1777526 TGGGGGTCCCCATTCCAGCTCACACTCTGTGGAGCTCAGATGCACCAGGTGGGTTACTTCCCTGG TGGGGGTCCCCATTCCAGCTCACACTCTGTGGGGCTCAGATGCACCAGGTGGGTTACTTCCCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1777517..1777844 26863196 MeRIP-seq:(Medium) rs972105460 Functional Loss SNV dbSNP153 33..33 33 - - - 76674 RMVar_ID_76674 Human_SNP_ID_170589632 m1A Human chr4 + 1797892 1797892 1797892 GGTGGGTTGGGCAGAAGAGGGCCTGGCCGGGCAGCCAGGGACTGGTGTGGCCAGAGTGGGCAGCT GGTGGGTTGGGCAGAAGAGGGCCTGGCCGGGCGGCCAGGGACTGGTGTGGCCAGAGTGGGCAGCT A G FGFR3 Ensembl:ENSG00000068078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1797886..1797970 26863196 MeRIP-seq:(Medium) rs926915619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1069355,Human_RBP_ID_3747883,Human_RBP_ID_5133579,Human_RBP_ID_5210871,Human_RBP_ID_5242071,Human_RBP_ID_5325921,Human_RBP_ID_5393968,Human_RBP_ID_8129750,Human_RBP_ID_8211527,Human_RBP_ID_8236374,Human_RBP_ID_8730089,Human_RBP_ID_9436333,Human_RBP_ID_17209124,Human_RBP_ID_18170184,Human_RBP_ID_18424540,Human_RBP_ID_21082512,Human_RBP_ID_22702280,Human_RBP_ID_22727055,Human_RBP_ID_22745546 RMVar_hsa_circ_121121,RMVar_hsa_circ_224271 76675 RMVar_ID_76675 Human_SNP_ID_170590494 m1A Human chr4 + 1799795 1799795 1799795 AGATGACGAAGACGGGGAGGACGAGGCTGAGGACACAGGTGTGGACACAGGTAGGAGCAGGGTCC AGATGACGAAGACGGGGAGGACGAGGCTGAGGGCACAGGTGTGGACACAGGTAGGAGCAGGGTCC A G FGFR3 Ensembl:ENSG00000068078 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1799713..1799869 26863196 MeRIP-seq:(Medium) rs781302593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837067,Human_RBP_ID_940513,Human_RBP_ID_8236376,Human_RBP_ID_18032813,Human_RBP_ID_19013487,Human_RBP_ID_26349056 Human_Splice_Rec_537968,Human_Splice_Rec_537969,Human_Splice_Rec_538002,Human_Splice_Rec_538003,Human_Splice_Rec_538034,Human_Splice_Rec_538035,Human_Splice_Rec_538068,Human_Splice_Rec_538069,Human_Splice_Rec_538098,Human_Splice_Rec_538099,Human_Splice_Rec_538132,Human_Splice_Rec_538133,Human_Splice_Rec_538160,Human_Splice_Rec_538161 RMVar_hsa_circ_82815,RMVar_hsa_circ_124967,RMVar_hsa_circ_121121,RMVar_hsa_circ_224271,RMVar_hsa_circ_100580,RMVar_hsa_circ_224273,RMVar_hsa_circ_224274,RMVar_hsa_circ_224272 76676 RMVar_ID_76676 Human_SNP_ID_170592057 m1A Human chr4 - 1803366 1803366 1803366 CAGGGACACACAGGCTGCGGAAGCGAGCAGGCAGCGGGCAGGGGTGGAGAGAGGCGCAAAGGGGT CAGGGACACACAGGCTGCGGAAGCGAGCAGGCGGCGGGCAGGGGTGGAGAGAGGCGCAAAGGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1803361..1803466 26863196 MeRIP-seq:(Medium) rs1363769699 Functional Loss SNV dbSNP153 33..33 33 - - - 76677 RMVar_ID_76677 Human_SNP_ID_170592699 m1A Human chr4 - 1804510 1804510 1804510 CCTGGTATCTACTTTCTGTTACCTGTCGCTTGAGCGGGAAGCGGGAGATCTTGTGCACGGTGGGG CCTGGTATCTACTTTCTGTTACCTGTCGCTTGGGCGGGAAGCGGGAGATCTTGTGCACGGTGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1804396..1804560 26863196 MeRIP-seq:(Medium) rs773239816 Functional Loss SNV dbSNP153 33..33 33 - - - 76678 RMVar_ID_76678 Human_SNP_ID_170593126 m1A Human chr4 - 1805450 1805450 1805450 CCTCACCTTTCAGCATCTTCACGGCTACGGTGACAGGCTTGGCGGCCCGGTCCTTGTCAATGCCG CCTCACCTTTCAGCATCTTCACGGCTACGGTGGCAGGCTTGGCGGCCCGGTCCTTGTCAATGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1805400..1805625 26863196 MeRIP-seq:(Medium) rs752724806 Functional Loss SNV dbSNP153 33..33 33 - - - 76679 RMVar_ID_76679 Human_SNP_ID_170594179 m1A Human chr4 - 1807274 1807274 1807274 TGGGCTGCTAGGGACCCCTCACATTGTTGGGGACCAGTGGCCCTTCACGTCCGCGAGCCCCCACT TGGGCTGCTAGGGACCCCTCACATTGTTGGGGGCCAGTGGCCCTTCACGTCCGCGAGCCCCCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1807226..1807387 26863196 MeRIP-seq:(Medium) rs758650628 Functional Loss SNV dbSNP153 33..33 33 - - - 76680 RMVar_ID_76680 Human_SNP_ID_170596661 m1A Human chr4 + 1814520 1814520 1814520 TTCTCCTCTTTTTCCAGTGTTGCTACAATCTCAGCCACCTGGCTGGTGGAGATGTGAACATCTTC TTCTCCTCTTTTTCCAGTGTTGCTACAATCTCTGCCACCTGGCTGGTGGAGATGTGAACATCTTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1814472..1814573 32194978 MeRIP-seq:(Medium) rs1298312246 Functional Loss SNV dbSNP153 33..33 33 - - - 76681 RMVar_ID_76681 Human_SNP_ID_170597424 m1A Human chr4 + 1816836 1816836 1816836 CTGCCCGATCATTTGCTGCACCCTTTTTGTCAATCTCTTGCTGGCTTTAGATTCTTCCACGTACT CTGCCCGATCATTTGCTGCACCCTTTTTGTCAGTCTCTTGCTGGCTTTAGATTCTTCCACGTACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1816785..1819475 26863196 MeRIP-seq:(Medium) rs532051187 Functional Loss SNV dbSNP153 33..33 33 - - - 76682 RMVar_ID_76682 Human_SNP_ID_170598098 m1A Human chr4 - 1819293 1819293 1819293 TGCTCCCTGGACTCTGAGACTGCAAGAAGAGTAAAATCGCTGTACTGGCCCCAAAAGTATACATA TGCTCCCTGGACTCTGAGACTGCAAGAAGAGTGAAATCGCTGTACTGGCCCCAAAAGTATACATA T C LETM1 Ensembl:ENSG00000168924 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1819291..1819523 26863196 MeRIP-seq:(Medium) rs976624112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77387,RMVar_hsa_circ_118259,RMVar_hsa_circ_88301,RMVar_hsa_circ_111913,RMVar_hsa_circ_83599,RMVar_hsa_circ_224280,RMVar_hsa_circ_224282,RMVar_hsa_circ_224283,RMVar_hsa_circ_224284,RMVar_hsa_circ_224281,RMVar_hsa_circ_340932,RMVar_hsa_circ_103901,RMVar_hsa_circ_30538,RMVar_hsa_circ_224285,RMVar_hsa_circ_53542 76683 RMVar_ID_76683 Human_SNP_ID_170607072 m1A Human chr4 - 1849197 1849197 1849197 TTCCCCTGTTCCTGTTACAGGTAGTCCAGGGGATCCTGCTCATCTCAGCTGTGCCAGCACCCTGG TTCCCCTGTTCCTGTTACAGGTAGTCCAGGGGTTCCTGCTCATCTCAGCTGTGCCAGCACCCTGG T A LETM1 Ensembl:ENSG00000168924 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1849188..1856047 32194978 MeRIP-seq:(Medium) rs764576993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_939877,Human_RBP_ID_4795257,Human_RBP_ID_5395082,Human_RBP_ID_22457795 Human_Splice_Rec_538212,Human_Splice_Rec_538213,Human_Splice_Rec_538252,Human_Splice_Rec_538253,Human_Splice_Rec_538264,Human_Splice_Rec_538265 Human_miRNA_ID_2064610,Human_miRNA_ID_2702485,Human_miRNA_ID_2933790 RMVar_hsa_circ_111913,RMVar_hsa_circ_224284,RMVar_hsa_circ_51890,RMVar_hsa_circ_344040 76684 RMVar_ID_76684 Human_SNP_ID_170608975 m1A Human chr4 + 1856040 1856040 1856040 CGCGGCTCTTCGCCGTCCCGGCGGCGCTTCAGACCCGGCCCGCGCGGACGGCTGACAGAGGCGGC CGCGGCTCTTCGCCGTCCCGGCGGCGCTTCAGCCCCGGCCCGCGCGGACGGCTGACAGAGGCGGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:1855951..1856150 26863410 MeRIP-seq:(Medium) rs965253823 Functional Loss SNV dbSNP153 33..33 33 - - - 76685 RMVar_ID_76685 Human_SNP_ID_170608976 m1A Human chr4 + 1856040 1856040 1856040 CGCGGCTCTTCGCCGTCCCGGCGGCGCTTCAGACCCGGCCCGCGCGGACGGCTGACAGAGGCGGC CGCGGCTCTTCGCCGTCCCGGCGGCGCTTCAGGCCCGGCCCGCGCGGACGGCTGACAGAGGCGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:1855951..1856150 26863410 MeRIP-seq:(Medium) rs965253823 Functional Loss SNV dbSNP153 33..33 33 - - - 76686 RMVar_ID_76686 Human_SNP_ID_170609942 m1A Human chr4 - 1859317 1859293 1859317 CTGGTTCCCTAAGCTCCCTAACTAGATCCCTAACTTCCTCCCTAACTAGATCCCTAGCCCCCCTT CTGGTTCCCTAAGCTCCCTAACTAGATCCCTA________________________GCCCCCCTT CTAGGGATCTAGTTAGGGAGGAAGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1859286..1859369 26863196 MeRIP-seq:(Medium) rs1173181657 Functional Loss DEL dbSNP153 33..56 33 - - - 76687 RMVar_ID_76687 Human_SNP_ID_170609953 m1A Human chr4 - 1859317 1859317 1859317 CTGGTTCCCTAAGCTCCCTAACTAGATCCCTAACTTCCTCCCTAACTAGATCCCTAGCCCCCCTT CTGGTTCCCTAAGCTCCCTAACTAGATCCCTAGCTTCCTCCCTAACTAGATCCCTAGCCCCCCTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1859286..1859369 26863196 MeRIP-seq:(Medium) rs1455621500 Functional Loss SNV dbSNP153 33..33 33 - - - 76688 RMVar_ID_76688 Human_SNP_ID_170613865 m1A Human chr4 + 1871710 1871710 1871710 GGGGGCACTGAGGAGGCCTGAGGGGCCGGCTCAGGGGCTGGGGGACCGGGAGGCCGGGCGGCCTG GGGGGCACTGAGGAGGCCTGAGGGGCCGGCTCCGGGGCTGGGGGACCGGGAGGCCGGGCGGCCTG A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:1871617..1871838 26863196 MeRIP-seq:(Medium) rs1171654037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266718,Human_RBP_ID_3747229,Human_RBP_ID_4794533,Human_RBP_ID_5150709,Human_RBP_ID_5210930,Human_RBP_ID_5241915,Human_RBP_ID_5325929,Human_RBP_ID_8130286,Human_RBP_ID_8211545,Human_RBP_ID_8236281,Human_RBP_ID_8730092,Human_RBP_ID_9334567,Human_RBP_ID_9435736,Human_RBP_ID_17155915,Human_RBP_ID_17195918,Human_RBP_ID_17661740,Human_RBP_ID_18424846,Human_RBP_ID_18465031,Human_RBP_ID_18500746,Human_RBP_ID_21988992,Human_RBP_ID_24384356,Human_RBP_ID_26771322,Human_RBP_ID_26791091 76689 RMVar_ID_76689 Human_SNP_ID_170613982 m1A Human chr4 + 1871943 1871943 1871943 CCCTGCGGCTGCACCTGTGCCCGGCCCGGCCGAGGCGGCCGCCTTTGTTCCCGCGGCGCCGAGCG CCCTGCGGCTGCACCTGTGCCCGGCCCGGCCGCGGCGGCCGCCTTTGTTCCCGCGGCGCCGAGCG A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1871935..1872311 26863196 MeRIP-seq:(Medium) rs1486348142 Functional Loss SNV dbSNP153 33..33 33 - - - 76690 RMVar_ID_76690 Human_SNP_ID_170616354 m1A Human chr4 + 1878735 1878735 1878735 GGTGTGAGCATTTTGCCTTGATGTGGAGTTGGAAAGGTGGAGGGCCATGGGCTGGTGGCAGAGGT GGTGTGAGCATTTTGCCTTGATGTGGAGTTGGGAAGGTGGAGGGCCATGGGCTGGTGGCAGAGGT A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1878732..1878938 26863196 MeRIP-seq:(Medium) rs948475535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5655259,Human_RBP_ID_15114154,Human_RBP_ID_17155455,Human_RBP_ID_23242625,Human_RBP_ID_24554206 76691 RMVar_ID_76691 Human_SNP_ID_170617182 m1A Human chr4 + 1881787 1881786 1881788 CAAGTCATGAAGGAAAGATCTAGGTGCATATAATAGGGAGGTTATACCTGACAAGGCTTTGGGAA CAAGTCATGAAGGAAAGATCTAGGTGCATATGACAGGGAGGTTATACCTGACAAGGCTTTGGGAA AAT GAC NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1881784..1882055 26863196 MeRIP-seq:(Medium) rs386670551 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_15114318 76692 RMVar_ID_76692 Human_SNP_ID_170617185 m1A Human chr4 + 1881793 1881793 1881793 ATGAAGGAAAGATCTAGGTGCATATAATAGGGAGGTTATACCTGACAAGGCTTTGGGAAAGACTT ATGAAGGAAAGATCTAGGTGCATATAATAGGGTGGTTATACCTGACAAGGCTTTGGGAAAGACTT A T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1881790..1882023 26863196 MeRIP-seq:(Medium) rs1020873437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15114318 76693 RMVar_ID_76693 Human_SNP_ID_170622840 m1A Human chr4 + 1900943 1900943 1900943 TGTTTAATGGAGAACCCGGCGCACACGATGCCAAACTGCGTTTTGAGTCCCAGGAAATGAAAGGG TGTTTAATGGAGAACCCGGCGCACACGATGCCCAACTGCGTTTTGAGTCCCAGGAAATGAAAGGG A C NSD2 Ensembl:ENSG00000109685 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1900892..1901242 32194978 MeRIP-seq:(Medium) rs909009733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618294,Human_RBP_ID_8881877,Human_RBP_ID_22095366,Human_RBP_ID_26825279,Human_RBP_ID_27326160 Human_miRNA_ID_242409,Human_miRNA_ID_1787975,Human_miRNA_ID_3097177,Human_miRNA_ID_3097178,Human_miRNA_ID_3097179,Human_miRNA_ID_3097180,Human_miRNA_ID_3097181 RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_17687,RMVar_hsa_circ_275779,RMVar_hsa_circ_17550,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323,RMVar_hsa_circ_49462,RMVar_hsa_circ_305754,RMVar_hsa_circ_360679,RMVar_hsa_circ_367366,RMVar_hsa_circ_315840,RMVar_hsa_circ_278843,RMVar_hsa_circ_33322,RMVar_hsa_circ_301012,RMVar_hsa_circ_224292,RMVar_hsa_circ_224293,RMVar_hsa_circ_308159,RMVar_hsa_circ_341117,RMVar_hsa_circ_288075,RMVar_hsa_circ_289851,RMVar_hsa_circ_282758,RMVar_hsa_circ_271096,RMVar_hsa_circ_273749,RMVar_hsa_circ_274051,RMVar_hsa_circ_273330,RMVar_hsa_circ_84134,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224296,RMVar_hsa_circ_224300,RMVar_hsa_circ_224302,RMVar_hsa_circ_224304,RMVar_hsa_circ_224305,RMVar_hsa_circ_224306,RMVar_hsa_circ_224303,RMVar_hsa_circ_224301,RMVar_hsa_circ_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295 76694 RMVar_ID_76694 Human_SNP_ID_170622841 m1A Human chr4 + 1900943 1900943 1900943 TGTTTAATGGAGAACCCGGCGCACACGATGCCAAACTGCGTTTTGAGTCCCAGGAAATGAAAGGG TGTTTAATGGAGAACCCGGCGCACACGATGCCGAACTGCGTTTTGAGTCCCAGGAAATGAAAGGG A G NSD2 Ensembl:ENSG00000109685 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1900892..1901242 32194978 MeRIP-seq:(Medium) rs909009733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618294,Human_RBP_ID_8881877,Human_RBP_ID_22095366,Human_RBP_ID_26825279,Human_RBP_ID_27326160 Human_miRNA_ID_242409,Human_miRNA_ID_1787975,Human_miRNA_ID_3097177,Human_miRNA_ID_3097178,Human_miRNA_ID_3097179,Human_miRNA_ID_3097180,Human_miRNA_ID_3097181 RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_17687,RMVar_hsa_circ_275779,RMVar_hsa_circ_17550,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323,RMVar_hsa_circ_49462,RMVar_hsa_circ_305754,RMVar_hsa_circ_360679,RMVar_hsa_circ_367366,RMVar_hsa_circ_315840,RMVar_hsa_circ_278843,RMVar_hsa_circ_33322,RMVar_hsa_circ_301012,RMVar_hsa_circ_224292,RMVar_hsa_circ_224293,RMVar_hsa_circ_308159,RMVar_hsa_circ_341117,RMVar_hsa_circ_288075,RMVar_hsa_circ_289851,RMVar_hsa_circ_282758,RMVar_hsa_circ_271096,RMVar_hsa_circ_273749,RMVar_hsa_circ_274051,RMVar_hsa_circ_273330,RMVar_hsa_circ_84134,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224296,RMVar_hsa_circ_224300,RMVar_hsa_circ_224302,RMVar_hsa_circ_224304,RMVar_hsa_circ_224305,RMVar_hsa_circ_224306,RMVar_hsa_circ_224303,RMVar_hsa_circ_224301,RMVar_hsa_circ_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295 76695 RMVar_ID_76695 Human_SNP_ID_170629272 m1A Human chr4 + 1924262 1924262 1924262 TTTCAGGCATGTTGGGGGAGGGTGCAGTGGCAAGCTCTGAATGGACACTCCAGTGTTTGACAGCT TTTCAGGCATGTTGGGGGAGGGTGCAGTGGCAGGCTCTGAATGGACACTCCAGTGTTTGACAGCT A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1924248..1924411 26863196 MeRIP-seq:(Medium) rs1162324304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15115646,Human_RBP_ID_24049215 RMVar_hsa_circ_224288,RMVar_hsa_circ_17687,RMVar_hsa_circ_305754,RMVar_hsa_circ_360679,RMVar_hsa_circ_367366,RMVar_hsa_circ_278843,RMVar_hsa_circ_33322,RMVar_hsa_circ_301012,RMVar_hsa_circ_224292,RMVar_hsa_circ_224293,RMVar_hsa_circ_341117,RMVar_hsa_circ_288075,RMVar_hsa_circ_289851,RMVar_hsa_circ_271096,RMVar_hsa_circ_273749,RMVar_hsa_circ_274051,RMVar_hsa_circ_84134,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224296,RMVar_hsa_circ_224300,RMVar_hsa_circ_224302,RMVar_hsa_circ_224301,RMVar_hsa_circ_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_267503,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295,RMVar_hsa_circ_224309,RMVar_hsa_circ_294907,RMVar_hsa_circ_310677,RMVar_hsa_circ_300305,RMVar_hsa_circ_352445,RMVar_hsa_circ_368346,RMVar_hsa_circ_224313 76696 RMVar_ID_76696 Human_SNP_ID_170630653 m1A Human chr4 + 1928631 1928610 1928631 CTTGTGAGGCGTGGTGGCTGTCTTGTGAGGCGAGGTGGCTGCAGGGCGCTTGTGACTCTGCTTTG CTTGTGAGGCGT_____________________GGTGGCTGCAGGGCGCTTGTGACTCTGCTTTG TGGTGGCTGTCTTGTGAGGCGA T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1928624..1929277 26863196 MeRIP-seq:(Medium) rs1158049323 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_15115758,Human_RBP_ID_18821965,Human_RBP_ID_24049220 RMVar_hsa_circ_224288,RMVar_hsa_circ_17687,RMVar_hsa_circ_305754,RMVar_hsa_circ_360679,RMVar_hsa_circ_367366,RMVar_hsa_circ_278843,RMVar_hsa_circ_33322,RMVar_hsa_circ_301012,RMVar_hsa_circ_224292,RMVar_hsa_circ_224293,RMVar_hsa_circ_341117,RMVar_hsa_circ_288075,RMVar_hsa_circ_289851,RMVar_hsa_circ_271096,RMVar_hsa_circ_273749,RMVar_hsa_circ_274051,RMVar_hsa_circ_84134,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224296,RMVar_hsa_circ_224300,RMVar_hsa_circ_224302,RMVar_hsa_circ_224301,RMVar_hsa_circ_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_267503,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295,RMVar_hsa_circ_224309,RMVar_hsa_circ_294907,RMVar_hsa_circ_310677,RMVar_hsa_circ_300305,RMVar_hsa_circ_352445,RMVar_hsa_circ_368346,RMVar_hsa_circ_224313 76697 RMVar_ID_76697 Human_SNP_ID_170630659 m1A Human chr4 + 1928631 1928631 1928631 CTTGTGAGGCGTGGTGGCTGTCTTGTGAGGCGAGGTGGCTGCAGGGCGCTTGTGACTCTGCTTTG CTTGTGAGGCGTGGTGGCTGTCTTGTGAGGCGTGGTGGCTGCAGGGCGCTTGTGACTCTGCTTTG A T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1928624..1929277 26863196 MeRIP-seq:(Medium) rs913189773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15115758,Human_RBP_ID_18821965,Human_RBP_ID_24049220 RMVar_hsa_circ_224288,RMVar_hsa_circ_17687,RMVar_hsa_circ_305754,RMVar_hsa_circ_360679,RMVar_hsa_circ_367366,RMVar_hsa_circ_278843,RMVar_hsa_circ_33322,RMVar_hsa_circ_301012,RMVar_hsa_circ_224292,RMVar_hsa_circ_224293,RMVar_hsa_circ_341117,RMVar_hsa_circ_288075,RMVar_hsa_circ_289851,RMVar_hsa_circ_271096,RMVar_hsa_circ_273749,RMVar_hsa_circ_274051,RMVar_hsa_circ_84134,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224296,RMVar_hsa_circ_224300,RMVar_hsa_circ_224302,RMVar_hsa_circ_224301,RMVar_hsa_circ_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_267503,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295,RMVar_hsa_circ_224309,RMVar_hsa_circ_294907,RMVar_hsa_circ_310677,RMVar_hsa_circ_300305,RMVar_hsa_circ_352445,RMVar_hsa_circ_368346,RMVar_hsa_circ_224313 76698 RMVar_ID_76698 Human_SNP_ID_170638004 m1A Human chr4 + 1955283 1955283 1955283 GCATCATCTGCACTGCCCACTTCACTGCTCGGAAGGGGAAGCGACACCACGCCCACGTCAACGTG GCATCATCTGCACTGCCCACTTCACTGCTCGGCAGGGGAAGCGACACCACGCCCACGTCAACGTG A C NSD2 Ensembl:ENSG00000109685 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1955232..1955333 32194978 MeRIP-seq:(Medium) rs980280785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837571,Human_RBP_ID_941580,Human_RBP_ID_9396076,Human_RBP_ID_15116829,Human_RBP_ID_18194997,Human_RBP_ID_19014189,Human_RBP_ID_23213714,Human_RBP_ID_27507621 Human_Splice_Rec_538289,Human_Splice_Rec_538367,Human_Splice_Rec_538409,Human_Splice_Rec_538449,Human_Splice_Rec_538515,Human_Splice_Rec_538559,Human_Splice_Rec_538649,Human_Splice_Rec_538671,Human_Splice_Rec_538685,Human_Splice_Rec_538691,Human_Splice_Rec_538713 RMVar_hsa_circ_341117,RMVar_hsa_circ_119169,RMVar_hsa_circ_51764,RMVar_hsa_circ_224294,RMVar_hsa_circ_311800,RMVar_hsa_circ_35994,RMVar_hsa_circ_71355,RMVar_hsa_circ_40407,RMVar_hsa_circ_38051,RMVar_hsa_circ_304919,RMVar_hsa_circ_275979,RMVar_hsa_circ_224316,RMVar_hsa_circ_116878,RMVar_hsa_circ_224317 76699 RMVar_ID_76699 Human_SNP_ID_170641745 m1A Human chr4 + 1969904 1969904 1969904 AGGATTGGGAACTTGTAGAACTCAGGAGTGAAACAAGGAAAAGAAAATTATTTTCTAAGCAAAGC AGGATTGGGAACTTGTAGAACTCAGGAGTGAAGCAAGGAAAAGAAAATTATTTTCTAAGCAAAGC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:1969901..1970226 26863196 MeRIP-seq:(Medium) rs1280031468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2841414,Human_RBP_ID_15117249 RMVar_hsa_circ_119169,RMVar_hsa_circ_224294,RMVar_hsa_circ_40407,RMVar_hsa_circ_322004 76700 RMVar_ID_76700 Human_SNP_ID_170641746 m1A Human chr4 + 1969913 1969913 1969913 AACTTGTAGAACTCAGGAGTGAAACAAGGAAAAGAAAATTATTTTCTAAGCAAAGCCTAAACCTC AACTTGTAGAACTCAGGAGTGAAACAAGGAAAGGAAAATTATTTTCTAAGCAAAGCCTAAACCTC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1969905..1970231 26863196 MeRIP-seq:(Medium) rs1436069103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2841414 RMVar_hsa_circ_119169,RMVar_hsa_circ_224294,RMVar_hsa_circ_40407,RMVar_hsa_circ_322004 76701 RMVar_ID_76701 Human_SNP_ID_170644575 m1A Human chr4 + 1978891 1978891 1978891 GGGAAGAGGCGGCGGCGGAGGGGCTGGCGGAGAGTCACAGAGGGCAAATAGCGCCAGGCGGCCGC GGGAAGAGGCGGCGGCGGAGGGGCTGGCGGAGGGTCACAGAGGGCAAATAGCGCCAGGCGGCCGC A G NSD2 Ensembl:ENSG00000109685 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr4:1978744..1979138;chr4:1978776..1979000;chr4:1978751..1979092 26863196 MeRIP-seq:(Medium) rs754212766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618407,Human_RBP_ID_3966579,Human_RBP_ID_5531134,Human_RBP_ID_9354467,Human_RBP_ID_27507636 RMVar_hsa_circ_119169,RMVar_hsa_circ_224294,RMVar_hsa_circ_377664,RMVar_hsa_circ_224319 76702 RMVar_ID_76702 Human_SNP_ID_170644656 m1A Human chr4 + 1979044 1979044 1979044 CGCCAGGACACAGACGTACAGGCCTCCTCGGGAGGGAGCGCCTCCCCACCACTGAGCCATCCTCA CGCCAGGACACAGACGTACAGGCCTCCTCGGGCGGGAGCGCCTCCCCACCACTGAGCCATCCTCA A C NSD2 Ensembl:ENSG00000109685 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:1979026..1979050 26863196 MeRIP-seq:(Medium) rs1347745578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248917,Human_RBP_ID_5531137,Human_RBP_ID_22096223 Human_miRNA_ID_2366295,Human_miRNA_ID_2366296,Human_miRNA_ID_2725045,Human_miRNA_ID_2725046,Human_miRNA_ID_3014101,Human_miRNA_ID_3014102 RMVar_hsa_circ_119169,RMVar_hsa_circ_224294,RMVar_hsa_circ_377664,RMVar_hsa_circ_224319 76703 RMVar_ID_76703 Human_SNP_ID_170644814 m1A Human chr4 - 1979401 1979401 1979401 CAGCCATTTCCAAAGAGCAGAGTAATGATCACAATGGCAGTTTCGAGGAATCCAGGGTCAGTCCT CAGCCATTTCCAAAGAGCAGAGTAATGATCACGATGGCAGTTTCGAGGAATCCAGGGTCAGTCCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1979351..1979425 32194978 MeRIP-seq:(Medium) rs1336775827 Functional Loss SNV dbSNP153 33..33 33 - - - 76704 RMVar_ID_76704 Human_SNP_ID_170645928 m1A Human chr4 + 1982863 1982863 1982863 TCCCAGGCAGGCACAGGCAGGGGACAAGGCCCACCGTCTCCCACGCTCTGGTGTGGTCGGGTGTC TCCCAGGCAGGCACAGGCAGGGGACAAGGCCCGCCGTCTCCCACGCTCTGGTGTGGTCGGGTGTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1982813..1982913 32194978 MeRIP-seq:(Medium) rs1440733129 Functional Loss SNV dbSNP153 33..33 33 - - - 76705 RMVar_ID_76705 Human_SNP_ID_170646128 m1A Human chr4 - 1983394 1983394 1983394 GGCCAGGGTAGCACAACCATGCTGGTGGACACAGTGTTTGAGATGAACTATGCCACGGGCCAGTG GGCCAGGGTAGCACAACCATGCTGGTGGACACGGTGTTTGAGATGAACTATGCCACGGGCCAGTG T C NELFA Ensembl:ENSG00000185049 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1983344..1983491 26863196 MeRIP-seq:(Medium) rs148813058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1975943,Human_RBP_ID_15117640 Human_miRNA_ID_2059239,Human_miRNA_ID_2184635,Human_miRNA_ID_2516491 RMVar_hsa_circ_83218,RMVar_hsa_circ_224322 76706 RMVar_ID_76706 Human_SNP_ID_170646449 m1A Human chr4 - 1984024 1984024 1984024 CGTTGCCAGCGCAGTTCAAGCAGCGGGCGCCCATGTACAACAGCGGCCTGAGCCCTGCCACACCC CGTTGCCAGCGCAGTTCAAGCAGCGGGCGCCCTTGTACAACAGCGGCCTGAGCCCTGCCACACCC T A NELFA Ensembl:ENSG00000185049 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1983826..1986391 26863196 MeRIP-seq:(Medium) rs772608553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26825285 Human_Splice_Rec_538740,Human_Splice_Rec_538752,Human_Splice_Rec_538772,Human_Splice_Rec_538790,Human_Splice_Rec_538810,Human_Splice_Rec_538828 RMVar_hsa_circ_83218,RMVar_hsa_circ_4559,RMVar_hsa_circ_224322 76707 RMVar_ID_76707 Human_SNP_ID_170646450 m1A Human chr4 - 1984024 1984024 1984024 CGTTGCCAGCGCAGTTCAAGCAGCGGGCGCCCATGTACAACAGCGGCCTGAGCCCTGCCACACCC CGTTGCCAGCGCAGTTCAAGCAGCGGGCGCCCGTGTACAACAGCGGCCTGAGCCCTGCCACACCC T C NELFA Ensembl:ENSG00000185049 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1983826..1986391 26863196 MeRIP-seq:(Medium) rs772608553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26825285 Human_Splice_Rec_538740,Human_Splice_Rec_538752,Human_Splice_Rec_538772,Human_Splice_Rec_538790,Human_Splice_Rec_538810,Human_Splice_Rec_538828 RMVar_hsa_circ_83218,RMVar_hsa_circ_4559,RMVar_hsa_circ_224322 76708 RMVar_ID_76708 Human_SNP_ID_170646763 m1A Human chr4 + 1984899 1984899 1984899 GGAAGGTAGCTCGTGGAGGGCAGCGCAGGCTCATTGTTCAGGGACCCAAGTTTCTGGAACACAGA GGAAGGTAGCTCGTGGAGGGCAGCGCAGGCTCGTTGTTCAGGGACCCAAGTTTCTGGAACACAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1984848..1985805 32194978 MeRIP-seq:(Medium) rs748549076 Functional Loss SNV dbSNP153 33..33 33 - - - 76709 RMVar_ID_76709 Human_SNP_ID_170648533 m1A Human chr4 - 1989801 1989799 1989802 AGTGCCAGTACTTGAACAAAAACGCCCTGACGACCCTCGCGGGACCCCTCACTCCCCCGGTGAAG AGTGCCAGTACTTGAACAAAAACGCCCTGAC___CCTCGCGGGACCCCTCACTCCCCCGGTGAAG GGTC G NELFA Ensembl:ENSG00000185049 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1989750..1989825 26863196 MeRIP-seq:(Medium) rs1444479532 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_538728,Human_Splice_Rec_538729,Human_Splice_Rec_538760,Human_Splice_Rec_538761,Human_Splice_Rec_538778,Human_Splice_Rec_538779,Human_Splice_Rec_538798,Human_Splice_Rec_538799,Human_Splice_Rec_538816,Human_Splice_Rec_538817,Human_Splice_Rec_538834,Human_Splice_Rec_538835,Human_Splice_Rec_538848,Human_Splice_Rec_538849,Human_Splice_Rec_538862,Human_Splice_Rec_538863,Human_Splice_Rec_538869,Human_Splice_Rec_538876,Human_Splice_Rec_538877,Human_Splice_Rec_538881,Human_Splice_Rec_538888,Human_Splice_Rec_538889 RMVar_hsa_circ_50384,RMVar_hsa_circ_4559,RMVar_hsa_circ_348181 76710 RMVar_ID_76710 Human_SNP_ID_170663968 m1A Human chr4 - 2042060 2042060 2042060 GGACGCCCGCACCACCGCCCTTACCGCGGTTCAGGGACCCCGGGACCAGCAGCGCGGGGACACCG GGACGCCCGCACCACCGCCCTTACCGCGGTTCGGGGACCCCGGGACCAGCAGCGCGGGGACACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:2042001..2042188;chr4:2042001..2042207;chr4:2042001..2042194;chr4:2042001..2042825 26863196 MeRIP-seq:(Medium) rs748563637 Functional Loss SNV dbSNP153 33..33 33 - - - 76711 RMVar_ID_76711 Human_SNP_ID_170664102 m1A Human chr4 + 2042382 2042382 2042382 CCATGGCCCCCCCGCCCGCGTGCCGGTCCCCGATGTCACCGCCGCCGCCGCCGCTGCTGCTGCTG CCATGGCCCCCCCGCCCGCGTGCCGGTCCCCGGTGTCACCGCCGCCGCCGCCGCTGCTGCTGCTG A G C4orf48 Ensembl:ENSG00000243449 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2042304..2042825 26863196 MeRIP-seq:(Medium) rs1451402029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4781694,Human_RBP_ID_5121120 Human_Splice_Rec_538902,Human_Splice_Rec_538908 76712 RMVar_ID_76712 Human_SNP_ID_170664119 m1A Human chr4 - 2042404 2042398 2042404 CCAGCAGCGCCAGACTCAGCAGCAGCAGCAGCAGCGGCGGCGGCGGCGGTGACATCGGGGACCGG CCAGCAGCGCCAGACTCAGCAGCAGCAGCAGC______GGCGGCGGCGGTGACATCGGGGACCGG CGCCGCT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:2042373..2042738 26863410 MeRIP-seq:(Medium) rs1423716921 Functional Loss DEL dbSNP153 33..38 33 - - - 76713 RMVar_ID_76713 Human_SNP_ID_170664136 m1A Human chr4 - 2042404 2042404 2042404 CCAGCAGCGCCAGACTCAGCAGCAGCAGCAGCAGCGGCGGCGGCGGCGGTGACATCGGGGACCGG CCAGCAGCGCCAGACTCAGCAGCAGCAGCAGCGGCGGCGGCGGCGGCGGTGACATCGGGGACCGG T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:2042373..2042738 26863410 MeRIP-seq:(Medium) rs1221710505 Functional Loss SNV dbSNP153 33..33 33 - - - 76714 RMVar_ID_76714 Human_SNP_ID_170669162 m1A Human chr4 + 2059679 2059679 2059679 CCCGGGCCGGCCGCCGCGCCCCCCGCGCCCCCACCTGCCCCGGTGGCTCAGCCTCACGGCGGGGC CCCGGGCCGGCCGCCGCGCCCCCCGCGCCCCCCCCTGCCCCGGTGGCTCAGCCTCACGGCGGGGC A C NAT8L Ensembl:ENSG00000185818 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:2059462..2059772 26863196 MeRIP-seq:(Medium) rs900199956 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_264920 76715 RMVar_ID_76715 Human_SNP_ID_170670736 m1A Human chr4 + 2064093 2064093 2064093 GCTGGCTGAGCGCCTCTTCTTCCAGGTCCGCTACCACCGCTACCGCCTGCAGCTGCGCGAGGAGT GCTGGCTGAGCGCCTCTTCTTCCAGGTCCGCTTCCACCGCTACCGCCTGCAGCTGCGCGAGGAGT A T NAT8L Ensembl:ENSG00000185818 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2064044..2064255 26863196 MeRIP-seq:(Medium) rs753738205 Functional Loss SNV dbSNP153 33..33 33 - - - 76716 RMVar_ID_76716 Human_SNP_ID_170670942 m1A Human chr4 + 2064554 2064554 2064554 AGCGCCACTGCCTGTGGAGGCCCCAGCTGGCCACGGCGCTGCTTTGCTCCGCGCATGCCGAGGGT AGCGCCACTGCCTGTGGAGGCCCCAGCTGGCCGCGGCGCTGCTTTGCTCCGCGCATGCCGAGGGT A G NAT8L Ensembl:ENSG00000185818 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2064506..2064580 26863196 MeRIP-seq:(Medium) rs980475073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18182891,Human_RBP_ID_26514914 Human_miRNA_ID_230737,Human_miRNA_ID_1811979 76717 RMVar_ID_76717 Human_SNP_ID_170671572 m1A Human chr4 - 2066551 2066551 2066551 GAGGGATGAGGTGGGCCAGGTCAGGCCCACCCACCAGGCACCCGGCCTCCAGCCCCGGGGGAGGA GAGGGATGAGGTGGGCCAGGTCAGGCCCACCCTCCAGGCACCCGGCCTCCAGCCCCGGGGGAGGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2066509..2066678 26863196 MeRIP-seq:(Medium) rs1438921241 Functional Loss SNV dbSNP153 33..33 33 - - - 76718 RMVar_ID_76718 Human_SNP_ID_170672381 m1A Human chr4 - 2068908 2068908 2068908 AACAATCTGCCCCCGCCGTGGGCTCACAGTACAGTTTCGGGAACAAACAGCAGCAGGTGAACCCC AACAATCTGCCCCCGCCGTGGGCTCACAGTACGGTTTCGGGAACAAACAGCAGCAGGTGAACCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2068858..2068963 26863196 MeRIP-seq:(Medium) rs983733675 Functional Loss SNV dbSNP153 33..33 33 - - - 76719 RMVar_ID_76719 Human_SNP_ID_170716927 m1A Human chr4 + 2241898 2241898 2241898 CACAGCCCCCGCCCCAGCTCCTCGCCCAGCGGACCGGGCCCTGATCCCCGGGCAGCTGCTGGAGC CACAGCCCCCGCCCCAGCTCCTCGCCCAGCGGTCCGGGCCCTGATCCCCGGGCAGCTGCTGGAGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:2241861..2242050 26863196 MeRIP-seq:(Medium) rs1433076658 Functional Loss SNV dbSNP153 33..33 33 - - - 76720 RMVar_ID_76720 Human_SNP_ID_170716997 m1A Human chr4 - 2242070 2242065 2242071 ACGGAGGGCGGTGGCGGCGGGCTCCTGCGAGAAGCAAGCGGAACTTCCTGAGGTGACTGACGCGG ACGGAGGGCGGTGGCGGCGGGCTCCTGCGAG______GCGGAACTTCCTGAGGTGACTGACGCGG CTTGCTT C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2241814..2242103 26863196 MeRIP-seq:(Medium) rs969504404 Functional Loss DEL dbSNP153 32..37 33 - - - Human_Splice_Rec_538961,Human_Splice_Rec_539097,Human_Splice_Rec_539231,Human_Splice_Rec_539239,Human_Splice_Rec_539249,Human_Splice_Rec_539253 76721 RMVar_ID_76721 Human_SNP_ID_170716998 m1A Human chr4 - 2242066 2242066 2242066 AGGGCGGTGGCGGCGGGCTCCTGCGAGAAGCAAGCGGAACTTCCTGAGGTGACTGACGCGGGCCT AGGGCGGTGGCGGCGGGCTCCTGCGAGAAGCATGCGGAACTTCCTGAGGTGACTGACGCGGGCCT T A HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2241849..2242114 26863196 MeRIP-seq:(Medium) rs1354152152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4782294,Human_RBP_ID_27326519 Human_Splice_Rec_538961,Human_Splice_Rec_539097,Human_Splice_Rec_539231,Human_Splice_Rec_539239,Human_Splice_Rec_539249,Human_Splice_Rec_539253 76722 RMVar_ID_76722 Human_SNP_ID_170716999 m1A Human chr4 - 2242067 2242067 2242067 GAGGGCGGTGGCGGCGGGCTCCTGCGAGAAGCAAGCGGAACTTCCTGAGGTGACTGACGCGGGCC GAGGGCGGTGGCGGCGGGCTCCTGCGAGAAGCCAGCGGAACTTCCTGAGGTGACTGACGCGGGCC T G HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:2241715..2242114;chr4:2241795..2242101 26863196 MeRIP-seq:(Medium) rs1209236094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4782294 Human_Splice_Rec_538961,Human_Splice_Rec_539097,Human_Splice_Rec_539231,Human_Splice_Rec_539239,Human_Splice_Rec_539249,Human_Splice_Rec_539253 76723 RMVar_ID_76723 Human_SNP_ID_170719100 m1A Human chr4 - 2248060 2248060 2248060 GCTGCAGGGACCAAGAGGCCATCACCGTGTCTATAGAGAGCAGACAGAAGCAGAACAGAGCCCGG GCTGCAGGGACCAAGAGGCCATCACCGTGTCTGTAGAGAGCAGACAGAAGCAGAACAGAGCCCGG T C MXD4 Ensembl:ENSG00000123933 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2248009..2248171 26863196 MeRIP-seq:(Medium) rs1025972600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618888,Human_RBP_ID_15126985,Human_RBP_ID_17209127 76724 RMVar_ID_76724 Human_SNP_ID_170719350 m1A Human chr4 - 2248823 2248823 2248823 TGGCCCATAGCAGTGCCTGCCGTGCCTCTGGTACATCTGTAGCCAATTCCCATATCATGGGGAAA TGGCCCATAGCAGTGCCTGCCGTGCCTCTGGTTCATCTGTAGCCAATTCCCATATCATGGGGAAA T A MXD4 Ensembl:ENSG00000123933 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2248773..2249320 32194978 MeRIP-seq:(Medium) rs544626265 Functional Loss SNV dbSNP153 33..33 33 - - - 76725 RMVar_ID_76725 Human_SNP_ID_170719878 m1A Human chr4 + 2250481 2250481 2250481 GGGCCTGTGGAGAGGCTGGCGTCAACTGAAGGAGAACTGGAGGGCTGACACGCGTGGCTGGCGGG GGGCCTGTGGAGAGGCTGGCGTCAACTGAAGGGGAACTGGAGGGCTGACACGCGTGGCTGGCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2250315..2250701 26863196 MeRIP-seq:(Medium) rs1378116645 Functional Loss SNV dbSNP153 33..33 33 - - - 76726 RMVar_ID_76726 Human_SNP_ID_170719892 m1A Human chr4 - 2250507 2250507 2250507 GTGCCCTCTGCTCCTTGGCCTGCCTGCCCGCCAGCCACGCGTGTCAGCCCTCCAGTTCTCCTTCA GTGCCCTCTGCTCCTTGGCCTGCCTGCCCGCCTGCCACGCGTGTCAGCCCTCCAGTTCTCCTTCA T A MXD4 Ensembl:ENSG00000123933 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2250463..2250619 26863196 MeRIP-seq:(Medium) rs756224237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1107597,Human_RBP_ID_5121122,Human_RBP_ID_17409425,Human_RBP_ID_17662059,Human_RBP_ID_27326555,Human_RBP_ID_27507902 76727 RMVar_ID_76727 Human_SNP_ID_170719893 m1A Human chr4 - 2250507 2250507 2250507 GTGCCCTCTGCTCCTTGGCCTGCCTGCCCGCCAGCCACGCGTGTCAGCCCTCCAGTTCTCCTTCA GTGCCCTCTGCTCCTTGGCCTGCCTGCCCGCCGGCCACGCGTGTCAGCCCTCCAGTTCTCCTTCA T C MXD4 Ensembl:ENSG00000123933 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2250463..2250619 26863196 MeRIP-seq:(Medium) rs756224237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1107597,Human_RBP_ID_5121122,Human_RBP_ID_17409425,Human_RBP_ID_17662059,Human_RBP_ID_27326555,Human_RBP_ID_27507902 76728 RMVar_ID_76728 Human_SNP_ID_170719988 m1A Human chr4 - 2250645 2250645 2250645 TTGGCCCTGGTGAGCTGGACAGTGTTGGCAGCAGCAGTGACGCGGACGACCACTACAGCCTGCAG TTGGCCCTGGTGAGCTGGACAGTGTTGGCAGCTGCAGTGACGCGGACGACCACTACAGCCTGCAG T A MXD4 Ensembl:ENSG00000123933 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2250226..2250647 26863196 MeRIP-seq:(Medium) rs969165930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795268,Human_RBP_ID_8589615,Human_RBP_ID_18024450,Human_RBP_ID_22533957,Human_RBP_ID_27507907 Human_Splice_Rec_539268,Human_Splice_Rec_539272,Human_Splice_Rec_539282 76729 RMVar_ID_76729 Human_SNP_ID_170720328 m1A Human chr4 + 2251469 2251469 2251469 AGCCAGGCGGTCACAGTCAGATGCCACCTCCCAGCCCTGTGGTTTCTGTCTACGGCCCAGCTCTA AGCCAGGCGGTCACAGTCAGATGCCACCTCCCGGCCCTGTGGTTTCTGTCTACGGCCCAGCTCTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2251468..2251727 26863196 MeRIP-seq:(Medium) rs1004791119 Functional Loss SNV dbSNP153 33..33 33 - - - 76730 RMVar_ID_76730 Human_SNP_ID_170722360 m1A Human chr4 - 2257841 2257841 2257841 TGCCAGGCTGTGTCCTTGTCTTGGGAATGGTCAGACTTGGAGGAGAAGGCTGAGGTCTGTTTCAG TGCCAGGCTGTGTCCTTGTCTTGGGAATGGTCTGACTTGGAGGAGAAGGCTGAGGTCTGTTTCAG T A MXD4 Ensembl:ENSG00000123933 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2257839..2257955 26863196 MeRIP-seq:(Medium) rs1165922757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5394678 RMVar_hsa_circ_100117,RMVar_hsa_circ_224348 76731 RMVar_ID_76731 Human_SNP_ID_170723857 m1A Human chr4 + 2261780 2261780 2261780 CAGGCCGGCCGCCTTTGTTTTCTCCCTGGCGAAGTCGCCGTCGAAGGGCAGCACCGAGGCGTAGC CAGGCCGGCCGCCTTTGTTTTCTCCCTGGCGATGTCGCCGTCGAAGGGCAGCACCGAGGCGTAGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2258888..2261996 32194978 MeRIP-seq:(Medium) rs1399441144 Functional Loss SNV dbSNP153 33..33 33 - - - 76732 RMVar_ID_76732 Human_SNP_ID_170726455 m1A Human chr4 - 2270324 2270324 2270324 GCCTCTGCTGTTGCGGTGAATCTGGAAGCCGGAGCAAGGGCCACTCCACAGGCTCTTTGGCACAG GCCTCTGCTGTTGCGGTGAATCTGGAAGCCGGGGCAAGGGCCACTCCACAGGCTCTTTGGCACAG T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2270281..2270386 32194978 MeRIP-seq:(Medium) rs1265944606 Functional Loss SNV dbSNP153 33..33 33 - - - 76733 RMVar_ID_76733 Human_SNP_ID_170733791 m1A Human chr4 - 2295527 2295525 2295527 AAAGACTTTTCTGAGAGAAGGAACGGCATCAGAGGCGGTAACGTGAGCATGGCGGTGAAGTGGTC AAAGACTTTTCTGAGAGAAGGAACGGCATCAG__GCGGTAACGTGAGCATGGCGGTGAAGTGGTC CCT C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2295504..2295697 26863196 MeRIP-seq:(Medium) rs1181218490 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_83131,RMVar_hsa_circ_224350 76734 RMVar_ID_76734 Human_SNP_ID_170751279 m1A Human chr4 - 2353645 2353645 2353645 GAGTGAGCAGGCTTCTGAGCCAAGGGGCAGCCAGTGTGGGAGGGGTGGGCCTGCCCAGGTGCTGG GAGTGAGCAGGCTTCTGAGCCAAGGGGCAGCCGGTGTGGGAGGGGTGGGCCTGCCCAGGTGCTGG T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2353630..2353750 26863196 MeRIP-seq:(Medium) rs1169723851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8129795,Human_RBP_ID_26771425,Human_RBP_ID_26791100 RMVar_hsa_circ_36996,RMVar_hsa_circ_356175,RMVar_hsa_circ_340031,RMVar_hsa_circ_337187,RMVar_hsa_circ_224354 76735 RMVar_ID_76735 Human_SNP_ID_170751302 m1A Human chr4 - 2353720 2353720 2353720 AGCCGGGCTGGAAGTGAGAAACCGCACGGGACACTTGGGGGAGCAGAGGCTGGGAGAGCGGGGGC AGCCGGGCTGGAAGTGAGAAACCGCACGGGACGCTTGGGGGAGCAGAGGCTGGGAGAGCGGGGGC T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:2353688..2353840 26863196 MeRIP-seq:(Medium) rs969595598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36996,RMVar_hsa_circ_356175,RMVar_hsa_circ_340031,RMVar_hsa_circ_337187,RMVar_hsa_circ_224354 76736 RMVar_ID_76736 Human_SNP_ID_170784213 m1A Human chr4 + 2469175 2469175 2469175 CTCGAGGAGCTCTCCTGGGCGGCTGAAGAAGGAGCTTCTTCTCCGGAGTGCGCCGGCGGTGGCGC CTCGAGGAGCTCTCCTGGGCGGCTGAAGAAGGGGCTTCTTCTCCGGAGTGCGCCGGCGGTGGCGC A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr4:2469126..2469276;chr4:2469126..2469250 26863196 MeRIP-seq:(Medium) rs1192368514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_619057,Human_RBP_ID_4782622,Human_RBP_ID_18424543,Human_RBP_ID_19014203,Human_RBP_ID_23034893,Human_RBP_ID_23120120 Human_Splice_Rec_539497,Human_Splice_Rec_539509,Human_Splice_Rec_539523,Human_Splice_Rec_539533,Human_Splice_Rec_539545,Human_Splice_Rec_539553,Human_Splice_Rec_539563,Human_Splice_Rec_539577,Human_Splice_Rec_539579,Human_Splice_Rec_539587,Human_Splice_Rec_539591,Human_Splice_Rec_539597,Human_Splice_Rec_539603,Human_Splice_Rec_539615,Human_Splice_Rec_539623,Human_Splice_Rec_539625 RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 76737 RMVar_ID_76737 Human_SNP_ID_170784215 m1A Human chr4 - 2469179 2469176 2469179 GCAGGCGCCACCGCCGGCGCACTCCGGAGAAGAAGCTCCTTCTTCAGCCGCCCAGGAGAGCTCCT GCAGGCGCCACCGCCGGCGCACTCCGGAGAAG___CTCCTTCTTCAGCCGCCCAGGAGAGCTCCT GCTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2469101..2469253 26863196 MeRIP-seq:(Medium) rs916745075 Functional Loss DEL dbSNP153 33..35 33 - - - 76738 RMVar_ID_76738 Human_SNP_ID_170784218 m1A Human chr4 - 2469179 2469179 2469179 GCAGGCGCCACCGCCGGCGCACTCCGGAGAAGAAGCTCCTTCTTCAGCCGCCCAGGAGAGCTCCT GCAGGCGCCACCGCCGGCGCACTCCGGAGAAGCAGCTCCTTCTTCAGCCGCCCAGGAGAGCTCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2469101..2469253 26863196 MeRIP-seq:(Medium) rs781007509 Functional Loss SNV dbSNP153 33..33 33 - - - 76739 RMVar_ID_76739 Human_SNP_ID_170784235 m1A Human chr4 + 2469189 2469189 2469189 CTGGGCGGCTGAAGAAGGAGCTTCTTCTCCGGAGTGCGCCGGCGGTGGCGCCTGCGGACCTAACT CTGGGCGGCTGAAGAAGGAGCTTCTTCTCCGGGGTGCGCCGGCGGTGGCGCCTGCGGACCTAACT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2469148..2469252 26863196 MeRIP-seq:(Medium) rs1034882224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_619057,Human_RBP_ID_4782622,Human_RBP_ID_18424543,Human_RBP_ID_18447489,Human_RBP_ID_19014203,Human_RBP_ID_23034893,Human_RBP_ID_23120120 Human_Splice_Rec_539497,Human_Splice_Rec_539509,Human_Splice_Rec_539523,Human_Splice_Rec_539533,Human_Splice_Rec_539545,Human_Splice_Rec_539553,Human_Splice_Rec_539563,Human_Splice_Rec_539577,Human_Splice_Rec_539579,Human_Splice_Rec_539587,Human_Splice_Rec_539591,Human_Splice_Rec_539597,Human_Splice_Rec_539603,Human_Splice_Rec_539615,Human_Splice_Rec_539623,Human_Splice_Rec_539625 RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 76740 RMVar_ID_76740 Human_SNP_ID_170791336 m1A Human chr4 - 2493132 2493132 2493132 CCACTCTGCTGTCTCTGAGCCTCCTCCTCCCAAGTAGCTTCCCTGCACCACTCAAGACAGGCTCA CCACTCTGCTGTCTCTGAGCCTCCTCCTCCCATGTAGCTTCCCTGCACCACTCAAGACAGGCTCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2493103..2493332 26863196 MeRIP-seq:(Medium) rs1187649254 Functional Loss SNV dbSNP153 33..33 33 - - - 76741 RMVar_ID_76741 Human_SNP_ID_170797255 m1A Human chr4 + 2512527 2512527 2512527 GTGTGGTGAGCAGTGACGATGAGGAGTTGTCCAGGGACAGAGACGTATATGTGACTACCCATACT GTGTGGTGAGCAGTGACGATGAGGAGTTGTCCGGGGACAGAGACGTATATGTGACTACCCATACT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2512476..2512550 32194978 MeRIP-seq:(Medium) rs1323628059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1637800,Human_RBP_ID_7301452,Human_RBP_ID_8879333,Human_RBP_ID_15130737,Human_RBP_ID_18024643,Human_RBP_ID_24051417 Human_Splice_Rec_539518,Human_Splice_Rec_539519,Human_Splice_Rec_539530,Human_Splice_Rec_539531,Human_Splice_Rec_539562,Human_Splice_Rec_539572,Human_Splice_Rec_539573,Human_Splice_Rec_539586,Human_Splice_Rec_539622,Human_Splice_Rec_539640,Human_Splice_Rec_539641,Human_Splice_Rec_539654,Human_Splice_Rec_539655,Human_Splice_Rec_539665 76742 RMVar_ID_76742 Human_SNP_ID_170797432 m1A Human chr4 - 2513079 2513079 2513079 AGATGGGACAACTGACAGTACCTGAGGGCCTAAGAGCACAGTGCTTCACGTTAGTTTCTCAGTCA AGATGGGACAACTGACAGTACCTGAGGGCCTAGGAGCACAGTGCTTCACGTTAGTTTCTCAGTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:2513076..2513150 32194978 MeRIP-seq:(Medium) rs757564554 Functional Loss SNV dbSNP153 33..33 33 - - - 76743 RMVar_ID_76743 Human_SNP_ID_170797647 m1A Human chr4 + 2513814 2513814 2513814 AGATCAACCACAAACGGTACCACCCCATTTATATATGAAGTATTCAGAGCCCCCCAGGAGAGACG AGATCAACCACAAACGGTACCACCCCATTTATGTATGAAGTATTCAGAGCCCCCCAGGAGAGACG A G RNF4 Ensembl:ENSG00000063978 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2513763..2513850 26863196 MeRIP-seq:(Medium) rs371680420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2844055,Human_RBP_ID_7301465,Human_RBP_ID_15130767,Human_RBP_ID_18024645,Human_RBP_ID_22826039 Human_miRNA_ID_1213997 76744 RMVar_ID_76744 Human_SNP_ID_170798097 m1A Human chr4 + 2515495 2515495 2515495 ATTGCCATTAACTTTCTTCTGGGCATCACGGCAATGTCACGATGCCCAGACTTGGAGCAAGGCAA ATTGCCATTAACTTTCTTCTGGGCATCACGGCGATGTCACGATGCCCAGACTTGGAGCAAGGCAA A G RNF4 Ensembl:ENSG00000063978 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1203257741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17407944,Human_RBP_ID_26515015 76745 RMVar_ID_76745 Human_SNP_ID_170805273 m1A Human chr4 + 2536765 2536764 2536766 CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCCAGCCCTCCCCGACCCGGACGCGACCCCGCGCAG CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCC__CCCTCCCCGACCCGGACGCGACCCCGCGCAG CAG C FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:2536689..2536876 26863196 MeRIP-seq:(Medium) rs1343359539 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4794838,Human_RBP_ID_5242086,Human_RBP_ID_5394686,Human_RBP_ID_9334604 76746 RMVar_ID_76746 Human_SNP_ID_170805274 m1A Human chr4 + 2536765 2536765 2536765 CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCCAGCCCTCCCCGACCCGGACGCGACCCCGCGCAG CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCCCGCCCTCCCCGACCCGGACGCGACCCCGCGCAG A C FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:2536689..2536876 26863196 MeRIP-seq:(Medium) rs1253620752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794838,Human_RBP_ID_5242086,Human_RBP_ID_5394686,Human_RBP_ID_9334604 76747 RMVar_ID_76747 Human_SNP_ID_170805275 m1A Human chr4 + 2536765 2536765 2536765 CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCCAGCCCTCCCCGACCCGGACGCGACCCCGCGCAG CAGCGGCCTGCCCCGCAGCTCCCGCCCGCCCCGGCCCTCCCCGACCCGGACGCGACCCCGCGCAG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:2536689..2536876 26863196 MeRIP-seq:(Medium) rs1253620752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794838,Human_RBP_ID_5242086,Human_RBP_ID_5394686,Human_RBP_ID_9334604 76748 RMVar_ID_76748 Human_SNP_ID_170805280 m1A Human chr4 + 2536776 2536776 2536776 CCCGCAGCTCCCGCCCGCCCCAGCCCTCCCCGACCCGGACGCGACCCCGCGCAGCGCCCCCCGGC CCCGCAGCTCCCGCCCGCCCCAGCCCTCCCCGCCCCGGACGCGACCCCGCGCAGCGCCCCCCGGC A C FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:2536727..2536910 26863196 MeRIP-seq:(Medium) rs1206919076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334604 76749 RMVar_ID_76749 Human_SNP_ID_170805388 m1A Human chr4 - 2537088 2537088 2537088 GAGGCCCGTTGGCCGCCGCCGCGCCGCCCACCAGGCCTGCCGCGCTGCCCGGGGCCGCCAGGCCC GAGGCCCGTTGGCCGCCGCCGCGCCGCCCACCGGGCCTGCCGCGCTGCCCGGGGCCGCCAGGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2536924..2537402 26863196 MeRIP-seq:(Medium) rs1370847482 Functional Loss SNV dbSNP153 33..33 33 - - - 76750 RMVar_ID_76750 Human_SNP_ID_170805404 m1A Human chr4 + 2537135 2537123 2537135 CGGCGGCCAACGGGCCTCTCGGCGCGGGCGCGAGCGCGGGCGGCGCCGCCCCCGGAGGCTACTTC CGGCGGCCAACGGGCCTCTCG____________GCGCGGGCGGCGCCGCCCCCGGAGGCTACTTC GGCGCGGGCGCGA G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2537100..2537384 26863196 MeRIP-seq:(Medium) rs930879620 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_940545,Human_RBP_ID_5531146,Human_RBP_ID_9334606,Human_RBP_ID_18465046,Human_RBP_ID_19013537,Human_RBP_ID_26791272 Human_Splice_Rec_539675 76751 RMVar_ID_76751 Human_SNP_ID_170805409 m1A Human chr4 + 2537135 2537135 2537135 CGGCGGCCAACGGGCCTCTCGGCGCGGGCGCGAGCGCGGGCGGCGCCGCCCCCGGAGGCTACTTC CGGCGGCCAACGGGCCTCTCGGCGCGGGCGCGGGCGCGGGCGGCGCCGCCCCCGGAGGCTACTTC A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2537100..2537384 26863196 MeRIP-seq:(Medium) rs1336825155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940545,Human_RBP_ID_5531146,Human_RBP_ID_9334606,Human_RBP_ID_18465046,Human_RBP_ID_19013537,Human_RBP_ID_26791272 Human_Splice_Rec_539675 76752 RMVar_ID_76752 Human_SNP_ID_170821063 m1A Human chr4 - 2587768 2587768 2587768 TTCTCTCACTGCCTATCTTTTCCTTCCTTTTCAGTGAATTCCTTCAGAGTTGTCCACCCCAGCTC TTCTCTCACTGCCTATCTTTTCCTTCCTTTTCGGTGAATTCCTTCAGAGTTGTCCACCCCAGCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2587757..2587986 26863196 MeRIP-seq:(Medium) rs772461626 Functional Loss SNV dbSNP153 33..33 33 - - - 76753 RMVar_ID_76753 Human_SNP_ID_170843513 m1A Human chr4 - 2663215 2663215 2663215 TCTCCTCTGTCCTGGGGCTCCTGCTTCCCAGCACTCCATCTTCCTTCGGGGCCCCTGGGGGCTCC TCTCCTCTGTCCTGGGGCTCCTGCTTCCCAGCCCTCCATCTTCCTTCGGGGCCCCTGGGGGCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2663164..2663231 26863196 MeRIP-seq:(Medium) rs995363623 Functional Loss SNV dbSNP153 33..33 33 - - - 76754 RMVar_ID_76754 Human_SNP_ID_170852968 m1A Human chr4 + 2696563 2696563 2696563 TCCGAAACCAAACCAGTGAGCAGCACGCGTGCAGCGAAGCGAGCAAGGCATAAGCAAAGGAAGGC TCCGAAACCAAACCAGTGAGCAGCACGCGTGCGGCGAAGCGAGCAAGGCATAAGCAAAGGAAGGC A G FAM193A Ensembl:ENSG00000125386 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:2696515..2696634;chr4:2696512..2696656 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9396093,Human_RBP_ID_27824631 RMVar_hsa_circ_356592,RMVar_hsa_circ_68554,RMVar_hsa_circ_373640,RMVar_hsa_circ_224361,RMVar_hsa_circ_75128,RMVar_hsa_circ_266476,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_6280,RMVar_hsa_circ_307706,RMVar_hsa_circ_347536,RMVar_hsa_circ_343600,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_366019,RMVar_hsa_circ_20005,RMVar_hsa_circ_224384,RMVar_hsa_circ_5845,RMVar_hsa_circ_62263,RMVar_hsa_circ_341113,RMVar_hsa_circ_333938,RMVar_hsa_circ_338965,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385 76755 RMVar_ID_76755 Human_SNP_ID_170853972 m1A Human chr4 + 2699778 2699775 2699778 CAGAGGCGGCGGGAGGAGGAGGAGGATGAGGAAGAAGAGGAGGATCGTTTCAAGGAGGAATTTCA CAGAGGCGGCGGGAGGAGGAGGAGGATGAG___GAAGAGGAGGATCGTTTCAAGGAGGAATTTCA GGAA G FAM193A Ensembl:ENSG00000125386 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2699659..2699828 26863196 MeRIP-seq:(Medium) rs773613254 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_22364173 Human_miRNA_ID_2997825 RMVar_hsa_circ_356592,RMVar_hsa_circ_68554,RMVar_hsa_circ_373640,RMVar_hsa_circ_224361,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_6280,RMVar_hsa_circ_307706,RMVar_hsa_circ_347536,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_366019,RMVar_hsa_circ_20005,RMVar_hsa_circ_224384,RMVar_hsa_circ_5845,RMVar_hsa_circ_62263,RMVar_hsa_circ_341113,RMVar_hsa_circ_333938,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_224387,RMVar_hsa_circ_270424,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 76756 RMVar_ID_76756 Human_SNP_ID_170853973 m1A Human chr4 + 2699778 2699778 2699778 CAGAGGCGGCGGGAGGAGGAGGAGGATGAGGAAGAAGAGGAGGATCGTTTCAAGGAGGAATTTCA CAGAGGCGGCGGGAGGAGGAGGAGGATGAGGAGGAAGAGGAGGATCGTTTCAAGGAGGAATTTCA A G FAM193A Ensembl:ENSG00000125386 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2699659..2699828 26863196 MeRIP-seq:(Medium) rs752774809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22364173 Human_miRNA_ID_2997825 RMVar_hsa_circ_356592,RMVar_hsa_circ_68554,RMVar_hsa_circ_373640,RMVar_hsa_circ_224361,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_6280,RMVar_hsa_circ_307706,RMVar_hsa_circ_347536,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_366019,RMVar_hsa_circ_20005,RMVar_hsa_circ_224384,RMVar_hsa_circ_5845,RMVar_hsa_circ_62263,RMVar_hsa_circ_341113,RMVar_hsa_circ_333938,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_224387,RMVar_hsa_circ_270424,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 76757 RMVar_ID_76757 Human_SNP_ID_170853974 m1A Human chr4 + 2699778 2699778 2699778 CAGAGGCGGCGGGAGGAGGAGGAGGATGAGGAAGAAGAGGAGGATCGTTTCAAGGAGGAATTTCA CAGAGGCGGCGGGAGGAGGAGGAGGATGAGGATGAAGAGGAGGATCGTTTCAAGGAGGAATTTCA A T FAM193A Ensembl:ENSG00000125386 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2699659..2699828 26863196 MeRIP-seq:(Medium) rs752774809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22364173 Human_miRNA_ID_2997825 RMVar_hsa_circ_356592,RMVar_hsa_circ_68554,RMVar_hsa_circ_373640,RMVar_hsa_circ_224361,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_6280,RMVar_hsa_circ_307706,RMVar_hsa_circ_347536,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_366019,RMVar_hsa_circ_20005,RMVar_hsa_circ_224384,RMVar_hsa_circ_5845,RMVar_hsa_circ_62263,RMVar_hsa_circ_341113,RMVar_hsa_circ_333938,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_224387,RMVar_hsa_circ_270424,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 76758 RMVar_ID_76758 Human_SNP_ID_170863895 m1A Human chr4 - 2732091 2732091 2732091 GAGGACTTGGCGGGAACTACTGTTCCAATCCGACAGCACAGAGCTACAATCGAAGGAGTCTCACG GAGGACTTGGCGGGAACTACTGTTCCAATCCGGCAGCACAGAGCTACAATCGAAGGAGTCTCACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2732042..2732251 26863196 MeRIP-seq:(Medium) rs1233351844 Functional Loss SNV dbSNP153 33..33 33 - - - 76759 RMVar_ID_76759 Human_SNP_ID_170867848 m1A Human chr4 + 2744877 2744877 2744877 TCGTGGGGGATCTGCAGCCCCCTGAGCTGCGCATGGAGCCCCCTCACGTATTCGTCCCTGCTGGC TCGTGGGGGATCTGCAGCCCCCTGAGCTGCGCGTGGAGCCCCCTCACGTATTCGTCCCTGCTGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:2744826..2744900 32194978 MeRIP-seq:(Medium) rs926751772 Functional Loss SNV dbSNP153 33..33 33 - - - 76760 RMVar_ID_76760 Human_SNP_ID_170868710 m1A Human chr4 - 2747840 2747840 2747840 ACGAGCGAGAGAAGGAAGTCGTCCTGCTACGGAGGAGCATGGCAGAAGGGGAGCGCGCCCGGGCC ACGAGCGAGAGAAGGAAGTCGTCCTGCTACGGGGGAGCATGGCAGAAGGGGAGCGCGCCCGGGCC T C TNIP2 Ensembl:ENSG00000168884 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2747791..2747925 26863196 MeRIP-seq:(Medium) rs1289832028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347174,RMVar_hsa_circ_224391,RMVar_hsa_circ_85395 76761 RMVar_ID_76761 Human_SNP_ID_170883049 m1A Human chr4 - 2795526 2795526 2795526 AGCCTGCCCTTCTCCTCACCCACCCAGGCTGCACAGTGATGGCCAAGCCACCCGGTTATTAAAGA AGCCTGCCCTTCTCCTCACCCACCCAGGCTGCGCAGTGATGGCCAAGCCACCCGGTTATTAAAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2795509..2795798 26863196 MeRIP-seq:(Medium) rs1159339660 Functional Loss SNV dbSNP153 33..33 33 - - - 76762 RMVar_ID_76762 Human_SNP_ID_170884267 m1A Human chr4 + 2799999 2799999 2799999 TCTGGAGACCACTGCCGAACATACGCCCTCCAAGCAGTGGCCACAAGAAGACCATGAGGAGCTCG TCTGGAGACCACTGCCGAACATACGCCCTCCACGCAGTGGCCACAAGAAGACCATGAGGAGCTCG A C SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2799996..2800077 26863196 MeRIP-seq:(Medium) rs1458635351 Functional Loss SNV dbSNP153 33..33 33 - - - 76763 RMVar_ID_76763 Human_SNP_ID_170886182 m1A Human chr4 + 2805660 2805660 2805660 GGAGGGGCAGATAGCCAACAGACATGCTGAAAATGCCACAGCGTCGGGGGGTGCCGGGTGGGGGC GGAGGGGCAGATAGCCAACAGACATGCTGAAAGTGCCACAGCGTCGGGGGGTGCCGGGTGGGGGC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2805658..2805868 26863196 MeRIP-seq:(Medium) rs1334822000 Functional Loss SNV dbSNP153 33..33 33 - - - 76764 RMVar_ID_76764 Human_SNP_ID_170889141 m1A Human chr4 + 2817383 2817383 2817383 GGATCCTTGAGGCAGGCCAGACAAGGGCACTGAGAACAGAGGCACAGAGATGGGACAGAGCCTCG GGATCCTTGAGGCAGGCCAGACAAGGGCACTGCGAACAGAGGCACAGAGATGGGACAGAGCCTCG A C SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2817101..2817444 26863196 MeRIP-seq:(Medium) rs1268689133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3748892 76765 RMVar_ID_76765 Human_SNP_ID_170889292 m1A Human chr4 - 2818113 2818113 2818113 GCGCCCCTCCCGGCCCCGCCCCCTGCCGCGTCACCGTGCGCGGGAGGCACGTGAGCCCCCTGCGG GCGCCCCTCCCGGCCCCGCCCCCTGCCGCGTCTCCGTGCGCGGGAGGCACGTGAGCCCCCTGCGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2818075..2818375 26863196 MeRIP-seq:(Medium) rs1048145854 Functional Loss SNV dbSNP153 33..33 33 - - - 76766 RMVar_ID_76766 Human_SNP_ID_170889297 m1A Human chr4 + 2818122 2818121 2818122 GCTCACGTGCCTCCCGCGCACGGTGACGCGGCAGGGGGCGGGGCCGGGAGGGGCGCGCCGGGATC GCTCACGTGCCTCCCGCGCACGGTGACGCGGC_GGGGGCGGGGCCGGGAGGGGCGCGCCGGGATC CA C SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2818107..2818270 26863196 MeRIP-seq:(Medium) rs1204873974 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3748897,Human_RBP_ID_26763768 76767 RMVar_ID_76767 Human_SNP_ID_170889299 m1A Human chr4 + 2818122 2818122 2818122 GCTCACGTGCCTCCCGCGCACGGTGACGCGGCAGGGGGCGGGGCCGGGAGGGGCGCGCCGGGATC GCTCACGTGCCTCCCGCGCACGGTGACGCGGCTGGGGGCGGGGCCGGGAGGGGCGCGCCGGGATC A T SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2818107..2818270 26863196 MeRIP-seq:(Medium) rs1465982371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3748897,Human_RBP_ID_26763768 76768 RMVar_ID_76768 Human_SNP_ID_170889438 m1A Human chr4 + 2818415 2818415 2818415 TGGACGCCGTGAGTACCGAGCCCCGGCCCCCGAGCCCCGGGACCCGGGCCGCGAGCTTCCGGCTC TGGACGCCGTGAGTACCGAGCCCCGGCCCCCGGGCCCCGGGACCCGGGCCGCGAGCTTCCGGCTC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2818405..2818609 26863196 MeRIP-seq:(Medium) rs7691803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211634 76769 RMVar_ID_76769 Human_SNP_ID_170891345 m1A Human chr4 - 2824818 2824818 2824818 TTTGCCCGGGGCTGAGAGGCCAGCGCCCCAGGACCAGCGAGCCCCCAAGGCAGGTCCAGCCTGGT TTTGCCCGGGGCTGAGAGGCCAGCGCCCCAGGTCCAGCGAGCCCCCAAGGCAGGTCCAGCCTGGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2824768..2825042 26863196 MeRIP-seq:(Medium) rs1183715258 Functional Loss SNV dbSNP153 33..33 33 - - - 76770 RMVar_ID_76770 Human_SNP_ID_170891358 m1A Human chr4 - 2824860 2824860 2824860 GCAGCACCCACCCAGCTGCCTGTGTCCCAGCCACACCTTCTCTTTGCCCGGGGCTGAGAGGCCAG GCAGCACCCACCCAGCTGCCTGTGTCCCAGCCTCACCTTCTCTTTGCCCGGGGCTGAGAGGCCAG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2824810..2825024 26863196 MeRIP-seq:(Medium) rs1349925847 Functional Loss SNV dbSNP153 33..33 33 - - - 76771 RMVar_ID_76771 Human_SNP_ID_170893421 m1A Human chr4 + 2830031 2830031 2830031 GAGGACCCCCCAAGGGAGGCAGCCATGCCCGGACTCTTTGTGCCCCCCGTGGCTCCCCGGCCTCC GAGGACCCCCCAAGGGAGGCAGCCATGCCCGGGCTCTTTGTGCCCCCCGTGGCTCCCCGGCCTCC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:2829899..2830057 26863196 MeRIP-seq:(Medium) rs770845820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_619511,Human_RBP_ID_940562 RMVar_hsa_circ_9936,RMVar_hsa_circ_38412,RMVar_hsa_circ_89980,RMVar_hsa_circ_96867,RMVar_hsa_circ_112687,RMVar_hsa_circ_224396,RMVar_hsa_circ_224397,RMVar_hsa_circ_224398 76772 RMVar_ID_76772 Human_SNP_ID_170895138 m1A Human chr4 + 2834813 2834813 2834813 GAGTTCACAGCCCAGTCTGGGGACAGCTGGGTATGAGGTGCTTACGGCACAGTGTCCAGGGCAGC GAGTTCACAGCCCAGTCTGGGGACAGCTGGGTGTGAGGTGCTTACGGCACAGTGTCCAGGGCAGC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2834762..2834863 32194978 MeRIP-seq:(Medium) rs369204065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 76773 RMVar_ID_76773 Human_SNP_ID_170897644 m1A Human chr4 - 2843924 2843924 2843924 GGCTCCGGCTCCGCCCCCGTCCCCTGGCCCGCAGCAGCGGCCCGCCAGGCCTCTCCGCCCCTCAG GGCTCCGGCTCCGCCCCCGTCCCCTGGCCCGCGGCAGCGGCCCGCCAGGCCTCTCCGCCCCTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr4:2843851..2844085;chr4:2843876..2844124;chr4:2843851..2844097 26863196 MeRIP-seq:(Medium) rs1474698812 Functional Loss SNV dbSNP153 33..33 33 - - - 76774 RMVar_ID_76774 Human_SNP_ID_170897675 m1A Human chr4 + 2843993 2843993 2843993 CCGACGGGCGGTGGCCGCACTGGGACCCCGGAATCCCGCGCGCTGCCCACGATTCGCTTCTGAGG CCGACGGGCGGTGGCCGCACTGGGACCCCGGAGTCCCGCGCGCTGCCCACGATTCGCTTCTGAGG A G ADD1 Ensembl:ENSG00000087274 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:2843905..2844023 26863196 MeRIP-seq:(Medium) rs1315384440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248845,Human_RBP_ID_619534,Human_RBP_ID_837161,Human_RBP_ID_4794542,Human_RBP_ID_8881889,Human_RBP_ID_9304111,Human_RBP_ID_9354468,Human_RBP_ID_9396101,Human_RBP_ID_9435960,Human_RBP_ID_18424545,Human_RBP_ID_23034896,Human_RBP_ID_23120122,Human_RBP_ID_26349826 Human_Splice_Rec_540309,Human_Splice_Rec_540321,Human_Splice_Rec_540351,Human_Splice_Rec_540379,Human_Splice_Rec_540387,Human_Splice_Rec_540415,Human_Splice_Rec_540423,Human_Splice_Rec_540427,Human_Splice_Rec_540457,Human_Splice_Rec_540473,Human_Splice_Rec_540479,Human_Splice_Rec_540509 Human_miRNA_ID_2249943 RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 76775 RMVar_ID_76775 Human_SNP_ID_170906990 m1A Human chr4 - 2878843 2878843 2878843 CCTGTTCTGAACTCCCTCACTGGCTTAGATCCATTGTAATGATTACATTGTAATCCCTTTCTTGC CCTGTTCTGAACTCCCTCACTGGCTTAGATCCCTTGTAATGATTACATTGTAATCCCTTTCTTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2878842..2879115 26863196 MeRIP-seq:(Medium) rs142028743 Functional Loss SNV dbSNP153 33..33 33 - - - 76776 RMVar_ID_76776 Human_SNP_ID_170907857 m1A Human chr4 + 2881952 2881952 2881952 CAATGATACAGGAGCAATTTAAGAAGGGGAAGAACCCCACAGGCCTATTGGCATTACAGCAGATT CAATGATACAGGAGCAATTTAAGAAGGGGAAGGACCCCACAGGCCTATTGGCATTACAGCAGATT A G ADD1 Ensembl:ENSG00000087274 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:2881901..2884606 32194978 MeRIP-seq:(Medium) rs113259674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3966605,Human_RBP_ID_9396105,Human_RBP_ID_18032561 Human_Splice_Rec_540312,Human_Splice_Rec_540324,Human_Splice_Rec_540354,Human_Splice_Rec_540390,Human_Splice_Rec_540420,Human_Splice_Rec_540430,Human_Splice_Rec_540460,Human_Splice_Rec_540482,Human_Splice_Rec_540516,Human_Splice_Rec_540550,Human_Splice_Rec_540586,Human_Splice_Rec_540602,Human_Splice_Rec_540630 RMVar_hsa_circ_9017,RMVar_hsa_circ_73156,RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_341844,RMVar_hsa_circ_224401,RMVar_hsa_circ_62360,RMVar_hsa_circ_342711,RMVar_hsa_circ_351542,RMVar_hsa_circ_273446,RMVar_hsa_circ_30215,RMVar_hsa_circ_46839,RMVar_hsa_circ_224402,RMVar_hsa_circ_224403,RMVar_hsa_circ_46430,RMVar_hsa_circ_327261,RMVar_hsa_circ_357559,RMVar_hsa_circ_224404,RMVar_hsa_circ_368555,RMVar_hsa_circ_351600,RMVar_hsa_circ_277455,RMVar_hsa_circ_312166,RMVar_hsa_circ_52057,RMVar_hsa_circ_224406,RMVar_hsa_circ_224408,RMVar_hsa_circ_20512,RMVar_hsa_circ_224407,RMVar_hsa_circ_224405 76777 RMVar_ID_76777 Human_SNP_ID_170907861 m1A Human chr4 + 2881958 2881958 2881958 TACAGGAGCAATTTAAGAAGGGGAAGAACCCCACAGGCCTATTGGCATTACAGCAGATTGCAGAT TACAGGAGCAATTTAAGAAGGGGAAGAACCCCCCAGGCCTATTGGCATTACAGCAGATTGCAGAT A C ADD1 Ensembl:ENSG00000087274 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2881863..2881969 26863196 MeRIP-seq:(Medium) rs891836805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3966605,Human_RBP_ID_9396105,Human_RBP_ID_18032561 Human_Splice_Rec_540312,Human_Splice_Rec_540324,Human_Splice_Rec_540354,Human_Splice_Rec_540390,Human_Splice_Rec_540420,Human_Splice_Rec_540430,Human_Splice_Rec_540460,Human_Splice_Rec_540482,Human_Splice_Rec_540516,Human_Splice_Rec_540550,Human_Splice_Rec_540586,Human_Splice_Rec_540602,Human_Splice_Rec_540630 RMVar_hsa_circ_9017,RMVar_hsa_circ_73156,RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_341844,RMVar_hsa_circ_224401,RMVar_hsa_circ_62360,RMVar_hsa_circ_342711,RMVar_hsa_circ_351542,RMVar_hsa_circ_273446,RMVar_hsa_circ_30215,RMVar_hsa_circ_46839,RMVar_hsa_circ_224402,RMVar_hsa_circ_224403,RMVar_hsa_circ_46430,RMVar_hsa_circ_327261,RMVar_hsa_circ_357559,RMVar_hsa_circ_224404,RMVar_hsa_circ_368555,RMVar_hsa_circ_351600,RMVar_hsa_circ_277455,RMVar_hsa_circ_312166,RMVar_hsa_circ_52057,RMVar_hsa_circ_224406,RMVar_hsa_circ_224408,RMVar_hsa_circ_20512,RMVar_hsa_circ_224407,RMVar_hsa_circ_224405 76778 RMVar_ID_76778 Human_SNP_ID_170913214 m1A Human chr4 - 2900954 2900954 2900954 CTATGACTGCACAGATCACAGGGGCAGGGCTCATTTGGGAATCGTTTGTCCATCTCTCTTATTAG CTATGACTGCACAGATCACAGGGGCAGGGCTCTTTTGGGAATCGTTTGTCCATCTCTCTTATTAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2900952..2901209 26863196 MeRIP-seq:(Medium) rs867131608 Functional Loss SNV dbSNP153 33..33 33 - - - 76779 RMVar_ID_76779 Human_SNP_ID_170913241 m1A Human chr4 - 2901079 2901076 2901080 GCTTCACTACCCTGGCTGGCCACCCAACTCTAACTGCTTCTTCAGCCTTCTTCATGAGCTTTTGC GCTTCACTACCCTGGCTGGCCACCCAACTCT____GCTTCTTCAGCCTTCTTCATGAGCTTTTGC CAGTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2901074..2901159 26863196 MeRIP-seq:(Medium) rs961788467 Functional Loss DEL dbSNP153 32..35 33 - - - 76780 RMVar_ID_76780 Human_SNP_ID_170915335 m1A Human chr4 + 2908974 2908974 2908974 CTCTTGTTCTGGTACATATTGCTGTCTGCAACAAAGTGCTGCTTGGGTTGCAGAGGGGTGGGTGC CTCTTGTTCTGGTACATATTGCTGTCTGCAACGAAGTGCTGCTTGGGTTGCAGAGGGGTGGGTGC A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:2908931..2909013 26863410 MeRIP-seq:(Medium) rs1245659793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21040925,Human_RBP_ID_22481511 RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_351542,RMVar_hsa_circ_327261,RMVar_hsa_circ_224408,RMVar_hsa_circ_27793,RMVar_hsa_circ_111946,RMVar_hsa_circ_224410,RMVar_hsa_circ_360285,RMVar_hsa_circ_4974,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_352144,RMVar_hsa_circ_224413,RMVar_hsa_circ_362025,RMVar_hsa_circ_79840,RMVar_hsa_circ_224416 76781 RMVar_ID_76781 Human_SNP_ID_170916980 m1A Human chr4 + 2914924 2914924 2914924 GGTGACGGCCTCCAAGGCCATCATTGAAAAGGAGTACCAGCCCCACGTCATTGTGAGCACCACGG GGTGACGGCCTCCAAGGCCATCATTGAAAAGGTGTACCAGCCCCACGTCATTGTGAGCACCACGG A T ADD1 Ensembl:ENSG00000087274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2914886..2914987 26863196 MeRIP-seq:(Medium) rs1173159818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8882102,Human_RBP_ID_9159397,Human_RBP_ID_27823963 Human_Splice_Rec_540344,Human_Splice_Rec_540374,Human_Splice_Rec_540410,Human_Splice_Rec_540450,Human_Splice_Rec_540502,Human_Splice_Rec_540538,Human_Splice_Rec_540570,Human_Splice_Rec_540622,Human_Splice_Rec_540650,Human_Splice_Rec_540676,Human_Splice_Rec_540686,Human_Splice_Rec_540692 RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_351542,RMVar_hsa_circ_327261,RMVar_hsa_circ_224408,RMVar_hsa_circ_27793,RMVar_hsa_circ_111946,RMVar_hsa_circ_224410,RMVar_hsa_circ_360285,RMVar_hsa_circ_4974,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_352144,RMVar_hsa_circ_224413,RMVar_hsa_circ_362025,RMVar_hsa_circ_224418,RMVar_hsa_circ_79840,RMVar_hsa_circ_224416,RMVar_hsa_circ_224417,RMVar_hsa_circ_328849 76782 RMVar_ID_76782 Human_SNP_ID_170920059 m1A Human chr4 - 2926114 2926114 2926114 CCCACAGTGGCGGCCGCTGCCACCCAGAGCTCACCTTCCTCCAGCTTGATGGGAGTGCTGGGAGG CCCACAGTGGCGGCCGCTGCCACCCAGAGCTCTCCTTCCTCCAGCTTGATGGGAGTGCTGGGAGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr4:2926079..2926150;chr4:2926091..2926339 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76783 RMVar_ID_76783 Human_SNP_ID_170920060 m1A Human chr4 - 2926114 2926114 2926114 CCCACAGTGGCGGCCGCTGCCACCCAGAGCTCACCTTCCTCCAGCTTGATGGGAGTGCTGGGAGG CCCACAGTGGCGGCCGCTGCCACCCAGAGCTCCCCTTCCTCCAGCTTGATGGGAGTGCTGGGAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr4:2926079..2926150;chr4:2926091..2926339 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76784 RMVar_ID_76784 Human_SNP_ID_170920798 m1A Human chr4 + 2928303 2928303 2928303 CTTCCCAATGTTAGAGAAGGAGGAGGAAGCCCATAGACCCCCAAGCCCCACTGAGGCCCCTACTG CTTCCCAATGTTAGAGAAGGAGGAGGAAGCCCGTAGACCCCCAAGCCCCACTGAGGCCCCTACTG A G ADD1 Ensembl:ENSG00000087274 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2928152..2928480 26863196 MeRIP-seq:(Medium) rs755347391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70866,Human_RBP_ID_619557,Human_RBP_ID_785718,Human_RBP_ID_9396975 RMVar_hsa_circ_111946,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 76785 RMVar_ID_76785 Human_SNP_ID_170920975 m1A Human chr4 + 2928705 2928704 2928705 CCGGGCTGACCCAGTGTGTGCTCAGCAGCCCCACCCCACCCTGCCCCTTGTCCTCTCAGAGCCTC CCGGGCTGACCCAGTGTGTGCTCAGCAGCCCC_CCCCACCCTGCCCCTTGTCCTCTCAGAGCCTC CA C ADD1 Ensembl:ENSG00000087274 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1248585739 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8211914,Human_RBP_ID_9304121,Human_RBP_ID_17296640,Human_RBP_ID_18955479,Human_RBP_ID_22095406,Human_RBP_ID_24052719,Human_RBP_ID_26518003 RMVar_hsa_circ_111946,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 76786 RMVar_ID_76786 Human_SNP_ID_170920976 m1A Human chr4 + 2928705 2928705 2928705 CCGGGCTGACCCAGTGTGTGCTCAGCAGCCCCACCCCACCCTGCCCCTTGTCCTCTCAGAGCCTC CCGGGCTGACCCAGTGTGTGCTCAGCAGCCCCCCCCCACCCTGCCCCTTGTCCTCTCAGAGCCTC A C ADD1 Ensembl:ENSG00000087274 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1273016720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211914,Human_RBP_ID_9304121,Human_RBP_ID_17296640,Human_RBP_ID_18955479,Human_RBP_ID_22095406,Human_RBP_ID_24052719,Human_RBP_ID_26518003 RMVar_hsa_circ_111946,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 76787 RMVar_ID_76787 Human_SNP_ID_170921087 m1A Human chr4 - 2929025 2929025 2929025 CCTGCCTCTTCAAGGCCGCTGGTGGGCACACGAGTGTTTTCACGGGACCAAGGCTTTGTATATAG CCTGCCTCTTCAAGGCCGCTGGTGGGCACACGGGTGTTTTCACGGGACCAAGGCTTTGTATATAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:2928851..2929150;chr4:2928876..2929150 26863196 MeRIP-seq:(Medium) rs1366104461 Functional Loss SNV dbSNP153 33..33 33 - - - 76788 RMVar_ID_76788 Human_SNP_ID_170921088 m1A Human chr4 - 2929025 2929025 2929025 CCTGCCTCTTCAAGGCCGCTGGTGGGCACACGAGTGTTTTCACGGGACCAAGGCTTTGTATATAG CCTGCCTCTTCAAGGCCGCTGGTGGGCACACGCGTGTTTTCACGGGACCAAGGCTTTGTATATAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:2928851..2929150;chr4:2928876..2929150 26863196 MeRIP-seq:(Medium) rs1366104461 Functional Loss SNV dbSNP153 33..33 33 - - - 76789 RMVar_ID_76789 Human_SNP_ID_170921326 m1A Human chr4 + 2929754 2929754 2929754 ATTGGCCAGCCGAGCGAGAACCAGGCTGCTGCATGGCACTGACCGCCGCTTCCAGCTTCCTCTGA ATTGGCCAGCCGAGCGAGAACCAGGCTGCTGCGTGGCACTGACCGCCGCTTCCAGCTTCCTCTGA A G ADD1 Ensembl:ENSG00000087274 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2929707..2929791 26863196 MeRIP-seq:(Medium) rs765380827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_619586,Human_RBP_ID_18195008,Human_RBP_ID_26515151 Human_miRNA_ID_206394 RMVar_hsa_circ_111946,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 76790 RMVar_ID_76790 Human_SNP_ID_170922488 m1A Human chr4 + 2932124 2932124 2932124 AGCAGGGCCAGGGGGCTGAGCAGATCAGCCGCATCACGGAACCCCAGGGCGATAGAGGGCGCCTG AGCAGGGCCAGGGGGCTGAGCAGATCAGCCGCGTCACGGAACCCCAGGGCGATAGAGGGCGCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2932073..2932500 26863196 MeRIP-seq:(Medium) rs369644394 Functional Loss SNV dbSNP153 33..33 33 - - - 76791 RMVar_ID_76791 Human_SNP_ID_170923323 m1A Human chr4 + 2933796 2933793 2933796 CGTGGCTCTCCAACAGCCCGGGCAGCAGGGGCAGCAGCAGCGTGAAGGCCAGGAGGTCCAGCAGG CGTGGCTCTCCAACAGCCCGGGCAGCAGGG___GCAGCAGCGTGAAGGCCAGGAGGTCCAGCAGG GGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2933559..2934435 26863196 MeRIP-seq:(Medium) rs1560285816 Functional Loss DEL dbSNP153 31..33 33 - - - 76792 RMVar_ID_76792 Human_SNP_ID_170923326 m1A Human chr4 + 2933796 2933796 2933796 CGTGGCTCTCCAACAGCCCGGGCAGCAGGGGCAGCAGCAGCGTGAAGGCCAGGAGGTCCAGCAGG CGTGGCTCTCCAACAGCCCGGGCAGCAGGGGCGGCAGCAGCGTGAAGGCCAGGAGGTCCAGCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2933559..2934435 26863196 MeRIP-seq:(Medium) rs551008690 Functional Loss SNV dbSNP153 33..33 33 - - - 76793 RMVar_ID_76793 Human_SNP_ID_170923389 m1A Human chr4 - 2933877 2933877 2933877 GGGTGGAGGCTGCACCCCGCGCCCACCCATCCACCAGCAGCCGCCGGAGCGCCGCGTGGTCACCG GGGTGGAGGCTGCACCCCGCGCCCACCCATCCCCCAGCAGCCGCCGGAGCGCCGCGTGGTCACCG T G MFSD10 Ensembl:ENSG00000109736 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:2933776..2933900 26863410 MeRIP-seq:(Medium) rs1476817626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794544,Human_RBP_ID_8130405,Human_RBP_ID_8212530,Human_RBP_ID_9334614,Human_RBP_ID_9435965,Human_RBP_ID_22457799 Human_Splice_Rec_540748,Human_Splice_Rec_540794,Human_Splice_Rec_540818,Human_Splice_Rec_540858,Human_Splice_Rec_540890 RMVar_hsa_circ_7810 76794 RMVar_ID_76794 Human_SNP_ID_170923392 m1A Human chr4 - 2933881 2933881 2933881 GAGGGGGTGGAGGCTGCACCCCGCGCCCACCCATCCACCAGCAGCCGCCGGAGCGCCGCGTGGTC GAGGGGGTGGAGGCTGCACCCCGCGCCCACCCGTCCACCAGCAGCCGCCGGAGCGCCGCGTGGTC T C MFSD10 Ensembl:ENSG00000109736 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:2933779..2933929 26863196 MeRIP-seq:(Medium) rs766439896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794544,Human_RBP_ID_8130405,Human_RBP_ID_8212530,Human_RBP_ID_9334614,Human_RBP_ID_9435965,Human_RBP_ID_22457799,Human_RBP_ID_27067392 Human_Splice_Rec_540748,Human_Splice_Rec_540794,Human_Splice_Rec_540818,Human_Splice_Rec_540858,Human_Splice_Rec_540890 RMVar_hsa_circ_7810 76795 RMVar_ID_76795 Human_SNP_ID_170923393 m1A Human chr4 - 2933881 2933881 2933881 GAGGGGGTGGAGGCTGCACCCCGCGCCCACCCATCCACCAGCAGCCGCCGGAGCGCCGCGTGGTC GAGGGGGTGGAGGCTGCACCCCGCGCCCACCCCTCCACCAGCAGCCGCCGGAGCGCCGCGTGGTC T G MFSD10 Ensembl:ENSG00000109736 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:2933779..2933929 26863196 MeRIP-seq:(Medium) rs766439896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794544,Human_RBP_ID_8130405,Human_RBP_ID_8212530,Human_RBP_ID_9334614,Human_RBP_ID_9435965,Human_RBP_ID_22457799,Human_RBP_ID_27067392 Human_Splice_Rec_540748,Human_Splice_Rec_540794,Human_Splice_Rec_540818,Human_Splice_Rec_540858,Human_Splice_Rec_540890 RMVar_hsa_circ_7810 76796 RMVar_ID_76796 Human_SNP_ID_170923403 m1A Human chr4 - 2933896 2933896 2933896 CCACCATGGGATGGGGAGGGGGTGGAGGCTGCACCCCGCGCCCACCCATCCACCAGCAGCCGCCG CCACCATGGGATGGGGAGGGGGTGGAGGCTGCTCCCCGCGCCCACCCATCCACCAGCAGCCGCCG T A MFSD10 Ensembl:ENSG00000109736 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2933776..2934442 26863196 MeRIP-seq:(Medium) rs1223106803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794544,Human_RBP_ID_8130405,Human_RBP_ID_8212530,Human_RBP_ID_9334614,Human_RBP_ID_9435965,Human_RBP_ID_22457799 Human_Splice_Rec_540748,Human_Splice_Rec_540794,Human_Splice_Rec_540818,Human_Splice_Rec_540858,Human_Splice_Rec_540890 RMVar_hsa_circ_7810 76797 RMVar_ID_76797 Human_SNP_ID_170923772 m1A Human chr4 + 2934720 2934720 2934720 CCCCGCGCGTCCCCTGTCCCACCCCCAACCCGAGCGCCCCCTACGCCCCCCACCCCGGGCGCCCC CCCCGCGCGTCCCCTGTCCCACCCCCAACCCGCGCGCCCCCTACGCCCCCCACCCCGGGCGCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2934716..2934794 26863196 MeRIP-seq:(Medium) rs1372487055 Functional Loss SNV dbSNP153 33..33 33 - - - 76798 RMVar_ID_76798 Human_SNP_ID_170925123 m1A Human chr4 - 2938358 2938358 2938358 GTGCCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC GTGCCACCACGCCCAGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs895833548 Functional Loss SNV dbSNP153 33..33 33 - - - 76799 RMVar_ID_76799 Human_SNP_ID_170925277 m1A Human chr4 - 2938644 2938644 2938644 AAAATTAGCCAAGTGTGGTGGCACGCACCTGTAGTCCCAACTACTCGGGAGGCTGAAGCAGGAGG AAAATTAGCCAAGTGTGGTGGCACGCACCTGTGGTCCCAACTACTCGGGAGGCTGAAGCAGGAGG T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1357965368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26515180 Human_miRNA_ID_276826 76800 RMVar_ID_76800 Human_SNP_ID_170925333 m1A Human chr4 - 2938759 2938759 2938759 TCACATCTGCAATTCCAACCCTCTGGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCG TCACATCTGCAATTCCAACCCTCTGGGAGGCCGAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCG T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1232820290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18025057,Human_RBP_ID_22826081 76801 RMVar_ID_76801 Human_SNP_ID_170928048 m1A Human chr4 + 2946141 2946139 2946141 TCACTCCAGATCACCCTCGCTGCCGTGCACTCACTCCAGATCACCCTCACTGCCGTGCACTCTCC TCACTCCAGATCACCCTCGCTGCCGTGCACT__CTCCAGATCACCCTCACTGCCGTGCACTCTCC TCA T NOP14-AS1 Ensembl:ENSG00000249673 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2946102..2946186 26863196 MeRIP-seq:(Medium) rs1226615505 Functional Loss DEL dbSNP153 32..33 33 - - - 76802 RMVar_ID_76802 Human_SNP_ID_170929165 m1A Human chr4 - 2950104 2950104 2950104 AGAAGGTGACAGTTCAGGCGGGGAGGACACAGAGGAGAGCGACAGCCCAGATAGCCACTTGGACC AGAAGGTGACAGTTCAGGCGGGGAGGACACAGGGGAGAGCGACAGCCCAGATAGCCACTTGGACC T C NOP14 Ensembl:ENSG00000087269 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:2949926..2950200;chr4:2949926..2951250 26863196 MeRIP-seq:(Medium) rs1181761911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70853,Human_RBP_ID_248843,Human_RBP_ID_7304257,Human_RBP_ID_8881900,Human_RBP_ID_9304305,Human_RBP_ID_9396118,Human_RBP_ID_21989272,Human_RBP_ID_24547644,Human_RBP_ID_26348875,Human_RBP_ID_27823967 Human_miRNA_ID_2552996 RMVar_hsa_circ_55392,RMVar_hsa_circ_55693,RMVar_hsa_circ_57701,RMVar_hsa_circ_62093,RMVar_hsa_circ_321141,RMVar_hsa_circ_326899,RMVar_hsa_circ_224425,RMVar_hsa_circ_286541,RMVar_hsa_circ_8626,RMVar_hsa_circ_363609,RMVar_hsa_circ_366233,RMVar_hsa_circ_324337,RMVar_hsa_circ_224427,RMVar_hsa_circ_65279,RMVar_hsa_circ_224426 76803 RMVar_ID_76803 Human_SNP_ID_170929185 m1A Human chr4 + 2950151 2950151 2950151 CCTGAACTGTCACCTTCTTCCTCGTTGCTCTCAGGGTCACTGGCTTCCTTGCTTTGCTCTTCCTG CCTGAACTGTCACCTTCTTCCTCGTTGCTCTCGGGGTCACTGGCTTCCTTGCTTTGCTCTTCCTG A G NOP14-AS1 Ensembl:ENSG00000249673 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2949926..2953576 26863196 MeRIP-seq:(Medium) rs1340476353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10978 76804 RMVar_ID_76804 Human_SNP_ID_170929467 m1A Human chr4 + 2951078 2951075 2951079 GAATACCAAAAAAATGTTTTTAAATTAAAAAAAGAGAGAGAAAGAGAAAATGAAGGCAAACATCT GAATACCAAAAAAATGTTTTTAAATTAAAA____AGAGAGAAAGAGAAAATGAAGGCAAACATCT AAAAG A NOP14-AS1 Ensembl:ENSG00000249673 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2951076..2951147 26863196 MeRIP-seq:(Medium) rs763892896 Functional Loss DEL dbSNP153 31..34 33 - - - 76805 RMVar_ID_76805 Human_SNP_ID_170929468 m1A Human chr4 + 2951078 2951076 2951079 GAATACCAAAAAAATGTTTTTAAATTAAAAAAAGAGAGAGAAAGAGAAAATGAAGGCAAACATCT GAATACCAAAAAAATGTTTTTAAATTAAAAA___AGAGAGAAAGAGAAAATGAAGGCAAACATCT AAAG A NOP14-AS1 Ensembl:ENSG00000249673 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:2951076..2951147 26863196 MeRIP-seq:(Medium) rs753808859 Functional Loss DEL dbSNP153 32..34 33 - - - 76806 RMVar_ID_76806 Human_SNP_ID_170929469 m1A Human chr4 + 2951077 2951077 2951077 TGAATACCAAAAAAATGTTTTTAAATTAAAAAAAGAGAGAGAAAGAGAAAATGAAGGCAAACATC TGAATACCAAAAAAATGTTTTTAAATTAAAAAGAGAGAGAGAAAGAGAAAATGAAGGCAAACATC A G NOP14-AS1 Ensembl:ENSG00000249673 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2951075..2951250 26863196 MeRIP-seq:(Medium) rs1553862953 Functional Loss SNV dbSNP153 33..33 33 - - - 76807 RMVar_ID_76807 Human_SNP_ID_170931448 m1A Human chr4 + 2957674 2957674 2957674 CTCGGGGCTCATGTTGCTGTTGTATTCTCCGAAGCGTTTATCTCTGAATACATTGGATTTATCCC CTCGGGGCTCATGTTGCTGTTGTATTCTCCGATGCGTTTATCTCTGAATACATTGGATTTATCCC A T NOP14-AS1 Ensembl:ENSG00000249673 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:2957626..2957781 26863196 MeRIP-seq:(Medium) rs1051189979 Functional Loss SNV dbSNP153 33..33 33 - - - 76808 RMVar_ID_76808 Human_SNP_ID_170933795 m1A Human chr4 - 2963003 2963001 2963003 CCTCGTTGAGCGGCACAGGCCGTGACAGGCACACGGCACTGACTTGATAGTCCGAAAGCCTCTGC CCTCGTTGAGCGGCACAGGCCGTGACAGGCAC__GGCACTGACTTGATAGTCCGAAAGCCTCTGC CGT C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2962999..2963107 32194978 MeRIP-seq:(Medium) rs1343902108 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8590460,Human_RBP_ID_23258807 76809 RMVar_ID_76809 Human_SNP_ID_170933797 m1A Human chr4 - 2963003 2963003 2963003 CCTCGTTGAGCGGCACAGGCCGTGACAGGCACACGGCACTGACTTGATAGTCCGAAAGCCTCTGC CCTCGTTGAGCGGCACAGGCCGTGACAGGCACGCGGCACTGACTTGATAGTCCGAAAGCCTCTGC T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2962999..2963107 32194978 MeRIP-seq:(Medium) rs1458036045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8590460,Human_RBP_ID_23258807 76810 RMVar_ID_76810 Human_SNP_ID_170933884 m1A Human chr4 - 2963222 2963222 2963222 GGGCCCGGCGAAGGCCAACTCCAATCCGTTCGAGGTGAAAGTTAACAGGCAGAAGTTCCAGATCC GGGCCCGGCGAAGGCCAACTCCAATCCGTTCGGGGTGAAAGTTAACAGGCAGAAGTTCCAGATCC T C NOP14 Ensembl:ENSG00000087269 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2957601..2963400 26863196 MeRIP-seq:(Medium) rs1380912385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12067,Human_RBP_ID_72480,Human_RBP_ID_4795757,Human_RBP_ID_15138910 Human_Splice_Rec_540983,Human_Splice_Rec_541017,Human_Splice_Rec_541051,Human_Splice_Rec_541083 76811 RMVar_ID_76811 Human_SNP_ID_170934138 m1A Human chr4 + 2963745 2963745 2963745 GGGGCTGCCCGGGGGCAGGGCACTGAGGAGGGAGTTGCGCGCGCGAGGCGAGGGCGATGGGGCCA GGGGCTGCCCGGGGGCAGGGCACTGAGGAGGGCGTTGCGCGCGCGAGGCGAGGGCGATGGGGCCA A C GRK4 Ensembl:ENSG00000125388 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2963654..2963957 26863196 MeRIP-seq:(Medium) rs1432439069 Functional Loss SNV dbSNP153 33..33 33 - - - 76812 RMVar_ID_76812 Human_SNP_ID_170992471 m1A Human chr4 + 3184097 3184097 3184097 AACACCGTACAGAAGAATCCAGGAGGGAAGAGAGTTAGGTGGTGTCTGCGGTGGGAGTGGCATTG AACACCGTACAGAAGAATCCAGGAGGGAAGAGGGTTAGGTGGTGTCTGCGGTGGGAGTGGCATTG A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3184049..3184159 26863196 MeRIP-seq:(Medium) rs892935058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329840,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_224464,RMVar_hsa_circ_224465,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224490,RMVar_hsa_circ_101101,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_224501,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_114515,RMVar_hsa_circ_224510,RMVar_hsa_circ_108449,RMVar_hsa_circ_125817,RMVar_hsa_circ_100165,RMVar_hsa_circ_123958,RMVar_hsa_circ_224511,RMVar_hsa_circ_101455,RMVar_hsa_circ_224514,RMVar_hsa_circ_224515,RMVar_hsa_circ_224516,RMVar_hsa_circ_111907,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_224518,RMVar_hsa_circ_363235,RMVar_hsa_circ_106414,RMVar_hsa_circ_21464,RMVar_hsa_circ_52143,RMVar_hsa_circ_224519,RMVar_hsa_circ_224524,RMVar_hsa_circ_303354,RMVar_hsa_circ_319173,RMVar_hsa_circ_81408,RMVar_hsa_circ_45374,RMVar_hsa_circ_104227,RMVar_hsa_circ_224525,RMVar_hsa_circ_377776,RMVar_hsa_circ_345984,RMVar_hsa_circ_224528,RMVar_hsa_circ_224530,RMVar_hsa_circ_305412,RMVar_hsa_circ_224527,RMVar_hsa_circ_326150,RMVar_hsa_circ_276279,RMVar_hsa_circ_224529 76813 RMVar_ID_76813 Human_SNP_ID_170992707 m1A Human chr4 + 3185137 3185137 3185137 GAAAAGGTTTTACTTGAAGAGGGAACGGAGAAATAGGGCAGTAGCCAGAGGAGGAGAGGAGTCGG GAAAAGGTTTTACTTGAAGAGGGAACGGAGAAGTAGGGCAGTAGCCAGAGGAGGAGAGGAGTCGG A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:3185129..3185240;chr4:3185089..3185232 26863196 MeRIP-seq:(Medium) rs149481207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329840,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_224464,RMVar_hsa_circ_224465,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224490,RMVar_hsa_circ_101101,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_224501,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_114515,RMVar_hsa_circ_224510,RMVar_hsa_circ_108449,RMVar_hsa_circ_125817,RMVar_hsa_circ_100165,RMVar_hsa_circ_123958,RMVar_hsa_circ_224511,RMVar_hsa_circ_101455,RMVar_hsa_circ_224514,RMVar_hsa_circ_224515,RMVar_hsa_circ_224516,RMVar_hsa_circ_111907,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_224518,RMVar_hsa_circ_363235,RMVar_hsa_circ_106414,RMVar_hsa_circ_21464,RMVar_hsa_circ_52143,RMVar_hsa_circ_224519,RMVar_hsa_circ_224524,RMVar_hsa_circ_303354,RMVar_hsa_circ_319173,RMVar_hsa_circ_81408,RMVar_hsa_circ_45374,RMVar_hsa_circ_104227,RMVar_hsa_circ_224525,RMVar_hsa_circ_377776,RMVar_hsa_circ_345984,RMVar_hsa_circ_224528,RMVar_hsa_circ_224530,RMVar_hsa_circ_305412,RMVar_hsa_circ_224527,RMVar_hsa_circ_326150,RMVar_hsa_circ_276279,RMVar_hsa_circ_224529 76814 RMVar_ID_76814 Human_SNP_ID_171007495 m1A Human chr4 + 3238490 3238490 3238490 GCTTTCCTTGTGAAGCCAGAGTGGTGGCCAGGATCCTGCCCCAGTTTCTAGACGACTTCTTCCCA GCTTTCCTTGTGAAGCCAGAGTGGTGGCCAGGGTCCTGCCCCAGTTTCTAGACGACTTCTTCCCA A G HTT Ensembl:ENSG00000197386 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3236247..3238897 32194978 MeRIP-seq:(Medium) rs1453173421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8881928,Human_RBP_ID_9304130 Human_Splice_Rec_541388,Human_Splice_Rec_541498 RMVar_hsa_circ_122246,RMVar_hsa_circ_224464,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_96024,RMVar_hsa_circ_224501,RMVar_hsa_circ_4660,RMVar_hsa_circ_110722,RMVar_hsa_circ_224546,RMVar_hsa_circ_64158,RMVar_hsa_circ_351583,RMVar_hsa_circ_56691 76815 RMVar_ID_76815 Human_SNP_ID_171007990 m1A Human chr4 - 3240008 3240008 3240008 TGGACATTTCGTAAACAAGTCAGCAGCCGGTGATATGGGCTTCCTGGGGCTGCAACCACCTCAAG TGGACATTTCGTAAACAAGTCAGCAGCCGGTGGTATGGGCTTCCTGGGGCTGCAACCACCTCAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3239963..3240613 32194978 MeRIP-seq:(Medium) rs362308 Functional Loss SNV dbSNP153 33..33 33 - - - 76816 RMVar_ID_76816 Human_SNP_ID_171025560 m1A Human chr4 + 3303071 3303071 3303071 AATGAATAAACGAATGAATGAGTGAGCAGGAAAATCATGGGGCCACGAGGAAGTGGGTCTGACCG AATGAATAAACGAATGAATGAGTGAGCAGGAAGATCATGGGGCCACGAGGAAGTGGGTCTGACCG A G RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3303058..3303325 26863196 MeRIP-seq:(Medium) rs1414049939 Functional Loss SNV dbSNP153 33..33 33 - - - 76817 RMVar_ID_76817 Human_SNP_ID_171027267 m1A Human chr4 + 3309312 3309310 3309313 AGCTGGGACTCGGGAATGGCAGGTGTCTGCTGAGGAGAACCGGGTGGGAGAGGAGCTGGGATCCG AGCTGGGACTCGGGAATGGCAGGTGTCTGCT___GAGAACCGGGTGGGAGAGGAGCTGGGATCCG TGAG T RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3309251..3309351 26863196 MeRIP-seq:(Medium) rs756799507 Functional Loss DEL dbSNP153 32..34 33 - - - 76818 RMVar_ID_76818 Human_SNP_ID_171027268 m1A Human chr4 + 3309315 3309315 3309315 TGGGACTCGGGAATGGCAGGTGTCTGCTGAGGAGAACCGGGTGGGAGAGGAGCTGGGATCCGGGA TGGGACTCGGGAATGGCAGGTGTCTGCTGAGGGGAACCGGGTGGGAGAGGAGCTGGGATCCGGGA A G RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3309255..3309361 26863196 MeRIP-seq:(Medium) rs3135147 Functional Loss SNV dbSNP153 33..33 33 - - - 76819 RMVar_ID_76819 Human_SNP_ID_171027921 m1A Human chr4 + 3310578 3310578 3310578 GGAAGGTCTGGGAAGAGTGGCCAGGGACTTGGAGGGCCTCTCAGGTGAATGATGGGAGGTGGCTG GGAAGGTCTGGGAAGAGTGGCCAGGGACTTGGTGGGCCTCTCAGGTGAATGATGGGAGGTGGCTG A T RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3310568..3310755 26863196 MeRIP-seq:(Medium) rs1310761821 Functional Loss SNV dbSNP153 33..33 33 - - - 76820 RMVar_ID_76820 Human_SNP_ID_171030065 m1A Human chr4 - 3317863 3317863 3317863 AGGAGGGGGCAGTGTGCCGCAGTTGATGCTGGACCAGCCATCGGTGGAATCTGTGTAAGAGTCCT AGGAGGGGGCAGTGTGCCGCAGTTGATGCTGGGCCAGCCATCGGTGGAATCTGTGTAAGAGTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3317489..3318040 32194978 MeRIP-seq:(Medium) rs866374138 Functional Loss SNV dbSNP153 33..33 33 - - - 76821 RMVar_ID_76821 Human_SNP_ID_171041527 m1A Human chr4 - 3361601 3361601 3361601 AGGGCCTTCCCTCGCTCCTGCTACCTGGCGCCAGTTCATGCCCTCGGTTTCCATCCCACCCGGCT AGGGCCTTCCCTCGCTCCTGCTACCTGGCGCCGGTTCATGCCCTCGGTTTCCATCCCACCCGGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3361501..3361730 26863196 MeRIP-seq:(Medium) rs1442230420 Functional Loss SNV dbSNP153 33..33 33 - - - 76822 RMVar_ID_76822 Human_SNP_ID_171042028 m1A Human chr4 - 3362816 3362814 3362816 ACACTCAGTCTCACACTCAAACACACTGACACACCCTCACTCTCATATTCACACACACCCTCACA ACACTCAGTCTCACACTCAAACACACTGACAC__CCTCACTCTCATATTCACACACACCCTCACA GGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3362354..3362878 26863196 MeRIP-seq:(Medium) rs546803998 Functional Loss DEL dbSNP153 33..34 33 - - - 76823 RMVar_ID_76823 Human_SNP_ID_171051547 m1A Human chr4 + 3397444 3397444 3397444 TTGGGAAGACAGGAAGAACCAGGAAAAAGCTGAGATGGCAGCCAGGGGGTCGCGAGGAACCCAAG TTGGGAAGACAGGAAGAACCAGGAAAAAGCTGCGATGGCAGCCAGGGGGTCGCGAGGAACCCAAG A C RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3397440..3397508 26863196 MeRIP-seq:(Medium) rs1330975842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64475 76824 RMVar_ID_76824 Human_SNP_ID_171056182 m1A Human chr4 - 3415077 3415066 3415078 ACGCGACCTCTCACACGCCCCTCACACACGCGACCTCACACGCCCCTCACACACAGGTGGCCCTC ACGCGACCTCTCACACGCCCCTCACACACGC____________CCCTCACACACAGGTGGCCCTC GGCGTGTGAGGTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3414839..3415230 26863196 MeRIP-seq:(Medium) rs1187410381 Functional Loss DEL dbSNP153 32..43 33 - - - 76825 RMVar_ID_76825 Human_SNP_ID_171061425 m1A Human chr4 + 3431526 3431526 3431526 GGGAGTGGAGGTGACGTCAGCAGCGCTCTCTGACCGCGGGTGTCACGGGCATTTCTCAAAGGAAG GGGAGTGGAGGTGACGTCAGCAGCGCTCTCTGTCCGCGGGTGTCACGGGCATTTCTCAAAGGAAG A T RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3431477..3431561 26863196 MeRIP-seq:(Medium) rs996947863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354469 RMVar_hsa_circ_116477,RMVar_hsa_circ_224556 76826 RMVar_ID_76826 Human_SNP_ID_171061435 m1A Human chr4 + 3431552 3431552 3431552 TCTCTGACCGCGGGTGTCACGGGCATTTCTCAAAGGAAGCAGGGGATTCAGTGAGTGTGAAGGTG TCTCTGACCGCGGGTGTCACGGGCATTTCTCAGAGGAAGCAGGGGATTCAGTGAGTGTGAAGGTG A G RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3431110..3431610 32194978 MeRIP-seq:(Medium) rs1258406889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116477,RMVar_hsa_circ_224556 76827 RMVar_ID_76827 Human_SNP_ID_171071507 m1A Human chr4 + 3463404 3463404 3463404 GAAGATGACCGAGGCGGCGCTGGTGGAGGGCCAGGTCAAGCTGCGGGACGGCAAGAAGGTCGGGG GAAGATGACCGAGGCGGCGCTGGTGGAGGGCCCGGTCAAGCTGCGGGACGGCAAGAAGGTCGGGG A C DOK7 Ensembl:ENSG00000175920 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3463353..3463454 26863196 MeRIP-seq:(Medium) rs1249658401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_541985,Human_Splice_Rec_541997,Human_Splice_Rec_542001,Human_Splice_Rec_542009,Human_Splice_Rec_542021 76828 RMVar_ID_76828 Human_SNP_ID_171071532 m1A Human chr4 - 3463441 3463441 3463441 CCGCGCCCGCGCCCCCCCCCCCCGCGCCCCCGACGCGCCCCGACCTTCTTGCCGTCCCGCAGCTT CCGCGCCCGCGCCCCCCCCCCCCGCGCCCCCGGCGCGCCCCGACCTTCTTGCCGTCCCGCAGCTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:3463436..3463562 26863196 MeRIP-seq:(Medium) rs1204938236 Functional Loss SNV dbSNP153 33..33 33 - - - 76829 RMVar_ID_76829 Human_SNP_ID_171071533 m1A Human chr4 - 3463441 3463441 3463441 CCGCGCCCGCGCCCCCCCCCCCCGCGCCCCCGACGCGCCCCGACCTTCTTGCCGTCCCGCAGCTT CCGCGCCCGCGCCCCCCCCCCCCGCGCCCCCGCCGCGCCCCGACCTTCTTGCCGTCCCGCAGCTT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:3463436..3463562 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76830 RMVar_ID_76830 Human_SNP_ID_171076051 m1A Human chr4 - 3475746 3475746 3475746 GGAAGGCTCTCTCTCCACAGCTGTGTGGCTCCATCACAGAAGGGGAAACCGAGGCTCAGGGATCC GGAAGGCTCTCTCTCCACAGCTGTGTGGCTCCGTCACAGAAGGGGAAACCGAGGCTCAGGGATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:3475640..3475794;chr4:3475443..3475805 26863196 MeRIP-seq:(Medium) rs888294766 Functional Loss SNV dbSNP153 33..33 33 - - - 76831 RMVar_ID_76831 Human_SNP_ID_171081741 m1A Human chr4 - 3490229 3490227 3490229 GAATGAGCAGGGAGAAAAGGAAGGAATGAATGAGGGGGTGAAGACAGGAATGAATGAGGGGGGAA GAATGAGCAGGGAGAAAAGGAAGGAATGAATG__GGGGTGAAGACAGGAATGAATGAGGGGGGAA CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3490226..3490370 26863196 MeRIP-seq:(Medium) rs1284395038 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24053816 76832 RMVar_ID_76832 Human_SNP_ID_171082131 m1A Human chr4 + 3490521 3490498 3490522 CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCACCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC CCTTCCTTTT________________________CCCCCCGCTCATTCGTTCCTTCCTTCTCCCC TCCCCCTGCTCATTCTTTCCTTCAC T DOK7 Ensembl:ENSG00000175920 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3490514..3490612 26863196 MeRIP-seq:(Medium) rs1229170333 Functional Loss DEL dbSNP153 11..34 33 - - - 76833 RMVar_ID_76833 Human_SNP_ID_171082171 m1A Human chr4 + 3490521 3490520 3490521 CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCACCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTC_CCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC CA C DOK7 Ensembl:ENSG00000175920 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3490514..3490612 26863196 MeRIP-seq:(Medium) rs1560227254 Functional Loss DEL dbSNP153 33..33 33 - - - 76834 RMVar_ID_76834 Human_SNP_ID_171082173 m1A Human chr4 + 3490521 3490521 3490521 CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCACCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCCCCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC A C DOK7 Ensembl:ENSG00000175920 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3490514..3490612 26863196 MeRIP-seq:(Medium) rs1297639878 Functional Loss SNV dbSNP153 33..33 33 - - - 76835 RMVar_ID_76835 Human_SNP_ID_171082174 m1A Human chr4 + 3490521 3490521 3490521 CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCACCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC CCTTCCTTTTCCCCCTGCTCATTCTTTCCTTCTCCCCCCCGCTCATTCGTTCCTTCCTTCTCCCC A T DOK7 Ensembl:ENSG00000175920 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3490514..3490612 26863196 MeRIP-seq:(Medium) rs1297639878 Functional Loss SNV dbSNP153 33..33 33 - - - 76836 RMVar_ID_76836 Human_SNP_ID_171082218 m1A Human chr4 - 3490569 3490560 3490570 AAGAAATGAAGGAATGAGCAGAGAGAGAAGGAAAAAACGAATGAGCAGGGGGAGAAGGAAGGAAC AAGAAATGAAGGAATGAGCAGAGAGAGAAGG__________TGAGCAGGGGGAGAAGGAAGGAAC ATTCGTTTTTT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3490435..3490687 26863196 MeRIP-seq:(Medium) rs1409034363 Functional Loss DEL dbSNP153 32..41 33 - - - 76837 RMVar_ID_76837 Human_SNP_ID_171082597 m1A Human chr4 - 3490938 3490923 3490938 GAAATGAGCAGGGGGAGAAGGAATGAATGAGCAGGGGAAGAAGGAAGGAATGAATGAGCAGAGGA GAAATGAGCAGGGGGAGAAGGAATGAATGAGC_______________GAATGAATGAGCAGAGGA CCTTCCTTCTTCCCCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3490888..3491142 26863196 MeRIP-seq:(Medium) rs1267912378 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_17069535 76838 RMVar_ID_76838 Human_SNP_ID_171091971 m1A Human chr4 + 3512875 3512875 3512875 ATCCTTCCTGCCTCGACACCCGTGCCAGCCCCAGCCACCCTGACGGCGGGCTGTCCACGGAAATG ATCCTTCCTGCCTCGACACCCGTGCCAGCCCCTGCCACCCTGACGGCGGGCTGTCCACGGAAATG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3512825..3513068 26863196 MeRIP-seq:(Medium) rs113953397 Functional Loss SNV dbSNP153 33..33 33 - - - 76839 RMVar_ID_76839 Human_SNP_ID_171092670 m1A Human chr4 - 3514852 3514852 3514852 CTACCAGAAGCAGCTGGAGATTGCGCACGAGAAGCTGAGGCACGCAGAGAGCGTGGGCGACGGCG CTACCAGAAGCAGCTGGAGATTGCGCACGAGAGGCTGAGGCACGCAGAGAGCGTGGGCGACGGCG T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:3514705..3514964 26863196 MeRIP-seq:(Medium) rs759659110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163020,Human_RBP_ID_9396148,Human_RBP_ID_18032822,Human_RBP_ID_22457805,Human_RBP_ID_22770218,Human_RBP_ID_26349137 Human_Splice_Rec_542056,Human_Splice_Rec_542070,Human_Splice_Rec_542086 76840 RMVar_ID_76840 Human_SNP_ID_171092696 m1A Human chr4 - 3514919 3514919 3514919 CACCTATGGAAACCTTGTTCCAGGAGGAGCTCAAGCACTTCGAAGCCAAAATCGAGAAGCACAAC CACCTATGGAAACCTTGTTCCAGGAGGAGCTCCAGCACTTCGAAGCCAAAATCGAGAAGCACAAC T G LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:3514869..3515923 26863410 MeRIP-seq:(Medium) rs759441276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72867,Human_RBP_ID_163020,Human_RBP_ID_249518,Human_RBP_ID_787114,Human_RBP_ID_939588,Human_RBP_ID_5210006,Human_RBP_ID_9396149,Human_RBP_ID_22679043,Human_RBP_ID_22770219 Human_Splice_Rec_542056,Human_Splice_Rec_542070,Human_Splice_Rec_542086 76841 RMVar_ID_76841 Human_SNP_ID_171093080 m1A Human chr4 + 3516074 3516074 3516074 TTTCCTTACCCGGAAACTGCAAGAGAATCTTCACCACAGGAGAGAGCTAGAAGGAGAGGGCCGTG TTTCCTTACCCGGAAACTGCAAGAGAATCTTCGCCACAGGAGAGAGCTAGAAGGAGAGGGCCGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3516071..3516200 32194978 MeRIP-seq:(Medium) rs199740578 Functional Loss SNV dbSNP153 33..33 33 - - - 76842 RMVar_ID_76842 Human_SNP_ID_171093106 m1A Human chr4 - 3516105 3516105 3516105 CAAGGAGCTGGAGGCGTTCCGGGTAAGGAAACACGGCCCTCTCCTTCTAGCTCTCTCCTGTGGTG CAAGGAGCTGGAGGCGTTCCGGGTAAGGAAACGCGGCCCTCTCCTTCTAGCTCTCTCCTGTGGTG T C LRPAP1 Ensembl:ENSG00000163956 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:3516101..3516150 26863196 MeRIP-seq:(Medium) rs1162818955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_542054,Human_Splice_Rec_542068,Human_Splice_Rec_542084,Human_Splice_Rec_542096 76843 RMVar_ID_76843 Human_SNP_ID_171094226 m1A Human chr4 - 3518917 3518917 3518917 CTCTGGCGGGAGTTCCTGCATCACAAAGAGAAAGTTCACGAGTACAACGTCCTGCTGGAGACCCT CTCTGGCGGGAGTTCCTGCATCACAAAGAGAAGGTTCACGAGTACAACGTCCTGCTGGAGACCCT T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3518901..3518925 26863196 MeRIP-seq:(Medium) rs1322965441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5120973,Human_RBP_ID_22457808,Human_RBP_ID_22770223,Human_RBP_ID_26349138 Human_Splice_Rec_542050,Human_Splice_Rec_542051,Human_Splice_Rec_542064,Human_Splice_Rec_542065,Human_Splice_Rec_542078,Human_Splice_Rec_542079,Human_Splice_Rec_542092,Human_Splice_Rec_542093,Human_Splice_Rec_542102,Human_Splice_Rec_542103 RMVar_hsa_circ_12234,RMVar_hsa_circ_366215 76844 RMVar_ID_76844 Human_SNP_ID_171094229 m1A Human chr4 - 3518927 3518927 3518927 ACTGGACAAGCTCTGGCGGGAGTTCCTGCATCACAAAGAGAAAGTTCACGAGTACAACGTCCTGC ACTGGACAAGCTCTGGCGGGAGTTCCTGCATCGCAAAGAGAAAGTTCACGAGTACAACGTCCTGC T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3518876..3519034 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_72869,Human_RBP_ID_5120973,Human_RBP_ID_22457643,Human_RBP_ID_22770224,Human_RBP_ID_26349138 Human_Splice_Rec_542050,Human_Splice_Rec_542051,Human_Splice_Rec_542064,Human_Splice_Rec_542065,Human_Splice_Rec_542078,Human_Splice_Rec_542079,Human_Splice_Rec_542092,Human_Splice_Rec_542093,Human_Splice_Rec_542102,Human_Splice_Rec_542103 RMVar_hsa_circ_12234,RMVar_hsa_circ_366215 76845 RMVar_ID_76845 Human_SNP_ID_171094640 m1A Human chr4 - 3520143 3520143 3520143 GTCTGGACGGAAAGAAGGACGCTCGGCAGGTGACCAGCAACTCCCTCAGTGGCACCCAGGAAGAC GTCTGGACGGAAAGAAGGACGCTCGGCAGGTGTCCAGCAACTCCCTCAGTGGCACCCAGGAAGAC T A LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:3520051..3520230;chr4:3520051..3520200 26863196 MeRIP-seq:(Medium) rs374080649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163022,Human_RBP_ID_249525,Human_RBP_ID_4784334,Human_RBP_ID_9397016,Human_RBP_ID_15144129,Human_RBP_ID_18823734,Human_RBP_ID_22457811,Human_RBP_ID_22770226,Human_RBP_ID_27327031,Human_RBP_ID_27508251 Human_Splice_Rec_542048,Human_Splice_Rec_542049,Human_Splice_Rec_542062,Human_Splice_Rec_542063,Human_Splice_Rec_542076,Human_Splice_Rec_542077,Human_Splice_Rec_542090,Human_Splice_Rec_542091,Human_Splice_Rec_542100,Human_Splice_Rec_542101 RMVar_hsa_circ_12234,RMVar_hsa_circ_366215,RMVar_hsa_circ_41357 76846 RMVar_ID_76846 Human_SNP_ID_171096323 m1A Human chr4 - 3524968 3524968 3524968 CAGGAGAGGGACGAACTCGCCTGGAAGAAACTAAAGCTTGACGGCTTGGACGAAGATGGGGAGAA CAGGAGAGGGACGAACTCGCCTGGAAGAAACTGAAGCTTGACGGCTTGGACGAAGATGGGGAGAA T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3524901..3525000 26863196 MeRIP-seq:(Medium) rs760432087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72871,Human_RBP_ID_619882,Human_RBP_ID_940233,Human_RBP_ID_4799319,Human_RBP_ID_9396155,Human_RBP_ID_15144236,Human_RBP_ID_22457812,Human_RBP_ID_22770229,Human_RBP_ID_24053924,Human_RBP_ID_26349140 Human_Splice_Rec_542046,Human_Splice_Rec_542047,Human_Splice_Rec_542060,Human_Splice_Rec_542061,Human_Splice_Rec_542074,Human_Splice_Rec_542075,Human_Splice_Rec_542089,Human_Splice_Rec_542098,Human_Splice_Rec_542099,Human_Splice_Rec_542106,Human_Splice_Rec_542107 RMVar_hsa_circ_366215,RMVar_hsa_circ_41357 76847 RMVar_ID_76847 Human_SNP_ID_171096951 m1A Human chr4 - 3526757 3526757 3526757 CTTCCTCCCAGGCCCAACACAGACTGAGCTGCAGGGAGCAGGATGGGCTCAGTCTAGATACAGGC CTTCCTCCCAGGCCCAACACAGACTGAGCTGCGGGGAGCAGGATGGGCTCAGTCTAGATACAGGC T C LRPAP1 Ensembl:ENSG00000163956 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3526756..3526850 26863196 MeRIP-seq:(Medium) rs954826836 Functional Loss SNV dbSNP153 33..33 33 - - - 76848 RMVar_ID_76848 Human_SNP_ID_171098326 m1A Human chr4 + 3531189 3531186 3531190 AACATTACGCCTGGGGCTTGACTGCTGGTCCCAGGAGCAGTTCAGGAAGGGCCTGTGGAGCTGAT AACATTACGCCTGGGGCTTGACTGCTGGTC____GAGCAGTTCAGGAAGGGCCTGTGGAGCTGAT CCCAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3531186..3531309 26863196 MeRIP-seq:(Medium) rs1402015611 Functional Loss DEL dbSNP153 31..34 33 - - - 76849 RMVar_ID_76849 Human_SNP_ID_171098791 m1A Human chr4 + 3532329 3532321 3532330 TTCTCCCGCGAGTACTTGCCGCCGTGGCTCGCAGCGGGCCAGGGCCCGAGGAAGAGCAGCAGCAG TTCTCCCGCGAGTACTTGCCGCCGT_________CGGGCCAGGGCCCGAGGAAGAGCAGCAGCAG TGGCTCGCAG T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:3532201..3532425 26863410 MeRIP-seq:(Medium) rs751647491 Functional Loss DEL dbSNP153 26..34 33 - - - 76850 RMVar_ID_76850 Human_SNP_ID_171098825 m1A Human chr4 + 3532366 3532366 3532366 GCCAGGGCCCGAGGAAGAGCAGCAGCAGTAGCAGCGCCGGGAGCCCGCGCAGAAACGACCTGACC GCCAGGGCCCGAGGAAGAGCAGCAGCAGTAGCGGCGCCGGGAGCCCGCGCAGAAACGACCTGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr4:3532148..3532425;chr4:3532132..3532425 26863196 MeRIP-seq:(Medium) rs1482673479 Functional Loss SNV dbSNP153 33..33 33 - - - 76851 RMVar_ID_76851 Human_SNP_ID_171098836 m1A Human chr4 + 3532375 3532375 3532375 CGAGGAAGAGCAGCAGCAGTAGCAGCGCCGGGAGCCCGCGCAGAAACGACCTGACCCTCCGCGGC CGAGGAAGAGCAGCAGCAGTAGCAGCGCCGGGGGCCCGCGCAGAAACGACCTGACCCTCCGCGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:3532149..3532425 26863196 MeRIP-seq:(Medium) rs1169601266 Functional Loss SNV dbSNP153 33..33 33 - - - 76852 RMVar_ID_76852 Human_SNP_ID_171179009 m1A Human chr4 + 3765969 3765934 3765969 CGGCGGCGGCGGCGGCGCAGCTCCGGCGAGCGAGGCGGCGGCCGCACGGCCAAGCGTGGACCGCG _________________________________GGCGGCGGCCGCACGGCCAAGCGTGGACCGCG CGGCGGCGGCGGCGGCGGCGCAGCTCCGGCGAGCGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3765919..3766182 26863196 MeRIP-seq:(Medium) rs1479647956 Functional Loss DEL dbSNP153 1..33 33 - - - 76853 RMVar_ID_76853 Human_SNP_ID_171179012 m1A Human chr4 + 3765969 3765940 3765969 CGGCGGCGGCGGCGGCGCAGCTCCGGCGAGCGAGGCGGCGGCCGCACGGCCAAGCGTGGACCGCG CGGC_____________________________GGCGGCGGCCGCACGGCCAAGCGTGGACCGCG CGGCGGCGGCGGCGCAGCTCCGGCGAGCGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3765919..3766182 26863196 MeRIP-seq:(Medium) rs1418796055 Functional Loss DEL dbSNP153 5..33 33 - - - 76854 RMVar_ID_76854 Human_SNP_ID_171179315 m1A Human chr4 + 3766799 3766772 3766799 TGGCTGCCGTGGTGGGCTTCCTCATCGTCTTCACCGTGGTGGGCAACGTGCTGGTGGTGATCGCC TGGCTG___________________________CCGTGGTGGGCAACGTGCTGGTGGTGATCGCC GCCGTGGTGGGCTTCCTCATCGTCTTCA G ADRA2C Ensembl:ENSG00000184160 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3766582..3766893 26863196 MeRIP-seq:(Medium) rs1165670311 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_786824,Human_RBP_ID_4795296,Human_RBP_ID_9354495,Human_RBP_ID_18464895,Human_RBP_ID_22096079,Human_RBP_ID_22727233,Human_RBP_ID_24054088 76855 RMVar_ID_76855 Human_SNP_ID_171179411 m1A Human chr4 - 3767009 3767009 3767009 GATGGCACACAGATGCACGATCGACGAGGTGCAAAACAGCACATCGAGCGCCAGGTACACGCCGC GATGGCACACAGATGCACGATCGACGAGGTGCGAAACAGCACATCGAGCGCCAGGTACACGCCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3766842..3767388 32194978 MeRIP-seq:(Medium) rs764847505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224559 76856 RMVar_ID_76856 Human_SNP_ID_171179607 m1A Human chr4 + 3767457 3767457 3767457 CGGGCACTGCGCGCCCCCGCCCGCCGACGTGGAGCCGGACGAGAGCAGCGCAGCGGCCGAGAGGC CGGGCACTGCGCGCCCCCGCCCGCCGACGTGGGGCCGGACGAGAGCAGCGCAGCGGCCGAGAGGC A G ADRA2C Ensembl:ENSG00000184160 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:3767409..3767550;chr4:3767406..3767535 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_619947,Human_RBP_ID_24384415 76857 RMVar_ID_76857 Human_SNP_ID_171179696 m1A Human chr4 - 3767678 3767644 3767678 GCACACGCTGCTGCGCGCCCGGCGCCGGCGCGACAGGAAGAACTCGACGGAGCGCGAGCTGGCGC GCACACGCTGCTGCGCGCCCGGCGCCGGCGCG_________________________________ GCGCGCCAGCTCGCGCTCCGTCGAGTTCTTCCTGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3767628..3767780 26863196 MeRIP-seq:(Medium) rs1295100439 Functional Loss DEL dbSNP153 33..65 33 - - - 76858 RMVar_ID_76858 Human_SNP_ID_171179717 m1A Human chr4 - 3767678 3767678 3767678 GCACACGCTGCTGCGCGCCCGGCGCCGGCGCGACAGGAAGAACTCGACGGAGCGCGAGCTGGCGC GCACACGCTGCTGCGCGCCCGGCGCCGGCGCGGCAGGAAGAACTCGACGGAGCGCGAGCTGGCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:3767628..3767780 26863196 MeRIP-seq:(Medium) rs1237400249 Functional Loss SNV dbSNP153 33..33 33 - - - 76859 RMVar_ID_76859 Human_SNP_ID_171244532 m1A Human chr4 - 3953151 3953151 3953151 CTCCACACAGAGCTTAGAAGCAAAGTTAAGAGACTCATCAGATTCTGAGCTGCGGCGGGATATTT CTCCACACAGAGCTTAGAAGCAAAGTTAAGAGGCTCATCAGATTCTGAGCTGCGGCGGGATATTT T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58515458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607578 Human_Splice_Rec_542142,Human_Splice_Rec_542143,Human_Splice_Rec_542172,Human_Splice_Rec_542173,Human_Splice_Rec_542180,Human_Splice_Rec_542181,Human_Splice_Rec_542188,Human_Splice_Rec_542189,Human_Splice_Rec_542192,Human_Splice_Rec_542193,Human_Splice_Rec_542198,Human_Splice_Rec_542199,Human_Splice_Rec_542211,Human_Splice_Rec_542215,Human_Splice_Rec_542222,Human_Splice_Rec_542223,Human_Splice_Rec_542230,Human_Splice_Rec_542231 76860 RMVar_ID_76860 Human_SNP_ID_171352895 m1A Human chr4 - 4248117 4248117 4248117 GGACGCCGAGGCCCAGCTGGACCGCGAGGGTGACGCCGGGCCGGGTGAGGCGCGCACCAAGCCGC GGACGCCGAGGCCCAGCTGGACCGCGAGGGTGGCGCCGGGCCGGGTGAGGCGCGCACCAAGCCGC T C TMEM128 Ensembl:ENSG00000132406 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:4248101..4248225 26863410 MeRIP-seq:(Medium) rs1174536807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249402,Human_RBP_ID_621233,Human_RBP_ID_4794847,Human_RBP_ID_18424546 Human_Splice_Rec_542263 76861 RMVar_ID_76861 Human_SNP_ID_171352930 m1A Human chr4 + 4248159 4248159 4248159 GGTCCAGCTGGGCCTCGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGC GGTCCAGCTGGGCCTCGGCGTCCGGCAGGAGGGGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:4248046..4248171 26863196 MeRIP-seq:(Medium) rs974680179 Functional Loss SNV dbSNP153 33..33 33 - - - 76862 RMVar_ID_76862 Human_SNP_ID_171352931 m1A Human chr4 + 4248159 4248159 4248159 GGTCCAGCTGGGCCTCGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGC GGTCCAGCTGGGCCTCGGCGTCCGGCAGGAGGTGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:4248046..4248171 26863196 MeRIP-seq:(Medium) rs974680179 Functional Loss SNV dbSNP153 33..33 33 - - - 76863 RMVar_ID_76863 Human_SNP_ID_171352934 m1A Human chr4 + 4248162 4248162 4248162 CCAGCTGGGCCTCGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGCGAG CCAGCTGGGCCTCGGCGTCCGGCAGGAGGAGGCATCGCCGCCGGAGCTGCTGCCGGGCCCGCGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:4248033..4248162 26863196 MeRIP-seq:(Medium) rs1169005051 Functional Loss SNV dbSNP153 33..33 33 - - - 76864 RMVar_ID_76864 Human_SNP_ID_171352947 m1A Human chr4 + 4248174 4248174 4248174 CGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGCGAGGAGTCCATCTTG CGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGGGCTGCTGCCGGGCCCGCGAGGAGTCCATCTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:4248080..4248200 26863196 MeRIP-seq:(Medium) rs1362444990 Functional Loss SNV dbSNP153 33..33 33 - - - 76865 RMVar_ID_76865 Human_SNP_ID_171352948 m1A Human chr4 + 4248174 4248174 4248174 CGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGAGCTGCTGCCGGGCCCGCGAGGAGTCCATCTTG CGGCGTCCGGCAGGAGGAGGAATCGCCGCCGGTGCTGCTGCCGGGCCCGCGAGGAGTCCATCTTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:4248080..4248200 26863196 MeRIP-seq:(Medium) rs1362444990 Functional Loss SNV dbSNP153 33..33 33 - - - 76866 RMVar_ID_76866 Human_SNP_ID_171364877 m1A Human chr4 - 4290089 4290089 4290089 CAGGTAGCTGCGGCGCTGGGCTGGCGGCGGCGAGTCCACGTGCTCCCCGCGGCCGGTTGAAACCG CAGGTAGCTGCGGCGCTGGGCTGGCGGCGGCGGGTCCACGTGCTCCCCGCGGCCGGTTGAAACCG T C LYAR Ensembl:ENSG00000145220 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:4289980..4290108;chr4:4289986..4290112;chr4:4289994..4290118 26863196 MeRIP-seq:(Medium) rs1322744200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794851,Human_RBP_ID_9334621,Human_RBP_ID_18026623 Human_Splice_Rec_542273 76867 RMVar_ID_76867 Human_SNP_ID_171366628 m1A Human chr4 + 4296143 4296143 4296143 GGACAGATCAGGGACATAGGAAGAGAACCAGAAGAGTTCTGGGACAGGAGGGATTTCAGGATGGG GGACAGATCAGGGACATAGGAAGAGAACCAGAGGAGTTCTGGGACAGGAGGGATTTCAGGATGGG A G ZBTB49 Ensembl:ENSG00000168826 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:4296142..4296216 26863196 MeRIP-seq:(Medium) rs1281834808 Functional Loss SNV dbSNP153 33..33 33 - - - 76868 RMVar_ID_76868 Human_SNP_ID_171405066 m1A Human chr4 - 4431736 4431733 4431736 CCTTGAGCTTTCTGACGTGGGTCATCAGGAGGAGGGAGGGTGCACAGAAGGTGGGCAGGCTGGGG CCTTGAGCTTTCTGACGTGGGTCATCAGGAGG___GAGGGTGCACAGAAGGTGGGCAGGCTGGGG CCCT C STX18 Ensembl:ENSG00000168818 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:4431732..4431863 26863196 MeRIP-seq:(Medium) rs1318865475 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_61144,RMVar_hsa_circ_318314,RMVar_hsa_circ_350414,RMVar_hsa_circ_352451,RMVar_hsa_circ_364512 76869 RMVar_ID_76869 Human_SNP_ID_171407233 m1A Human chr4 - 4439776 4439774 4439776 GATGCCCTGGGAAGAGCCCGTGGGGAAGAAACAGGGGAATGCCAAGTGCAGAGGACTCAGTCCTG GATGCCCTGGGAAGAGCCCGTGGGGAAGAAAC__GGGAATGCCAAGTGCAGAGGACTCAGTCCTG CCT C STX18 Ensembl:ENSG00000168818 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:4439747..4439812 26863196 MeRIP-seq:(Medium) rs1259750851 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17209173,Human_RBP_ID_24056445 RMVar_hsa_circ_61144,RMVar_hsa_circ_350414,RMVar_hsa_circ_33031,RMVar_hsa_circ_335894,RMVar_hsa_circ_314569,RMVar_hsa_circ_267258 76870 RMVar_ID_76870 Human_SNP_ID_171415191 m1A Human chr4 + 4471704 4471704 4471704 AGAAGAAAATCTCTCAGTTTGCCAATGTGAGAAATCTAAAATTAAAAAAGAAAGCCAACAGTTTA AGAAGAAAATCTCTCAGTTTGCCAATGTGAGAGATCTAAAATTAAAAAAGAAAGCCAACAGTTTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:4471687..4471774 26863196 MeRIP-seq:(Medium) rs745482364 Functional Loss SNV dbSNP153 33..33 33 - - - 76871 RMVar_ID_76871 Human_SNP_ID_171433376 m1A Human chr4 + 4542296 4542281 4542296 GTTTGGGGCGTGTGGGCTCCGGGAGCGTGAGGACCGGGAAGCTAGGAGGCTCCTTCCCTTCTGGC GTTTGGGGCGTGTGGGCT_______________CCGGGAAGCTAGGAGGCTCCTTCCCTTCTGGC TCCGGGAGCGTGAGGA T STX18-AS1 Ensembl:ENSG00000247708 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:4542250..4542374 26863196 MeRIP-seq:(Medium) rs1259336109 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_1139938,Human_RBP_ID_5608181 RMVar_hsa_circ_224577,RMVar_hsa_circ_120232 76872 RMVar_ID_76872 Human_SNP_ID_171475054 m1A Human chr4 + 4703060 4703060 4703060 TAGGGTGGAGGTGTGCGAGGGATTTCAGAACCAGAGAAGAAGGAGTCTGAACCTGCTGGGGCTGT TAGGGTGGAGGTGTGCGAGGGATTTCAGAACCGGAGAAGAAGGAGTCTGAACCTGCTGGGGCTGT A G STX18-AS1 Ensembl:ENSG00000247708 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:4702945..4703128 26863196 MeRIP-seq:(Medium) rs1453266216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307790,RMVar_hsa_circ_77701,RMVar_hsa_circ_224584,RMVar_hsa_circ_224586 76873 RMVar_ID_76873 Human_SNP_ID_171487822 m1A Human chr4 - 4755778 4755778 4755778 AAATTCAGTGAGTTTCCCGCAGTGCCCCAAAGAGCCGGAGGAGCCTGGGGCCATCCCTTAAGGGT AAATTCAGTGAGTTTCCCGCAGTGCCCCAAAGGGCCGGAGGAGCCTGGGGCCATCCCTTAAGGGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:4755657..4755795 26863196 MeRIP-seq:(Medium) rs539684041 Functional Loss SNV dbSNP153 33..33 33 - - - 76874 RMVar_ID_76874 Human_SNP_ID_171515871 m1A Human chr4 - 4859928 4859928 4859928 AGGCGGAGTCCTCCACTTTGACACCGAGTGGCAAAGAAGTCATGTCAGCAGCCGGGGCCATGCAG AGGCGGAGTCCTCCACTTTGACACCGAGTGGCGAAGAAGTCATGTCAGCAGCCGGGGCCATGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:4859813..4859962 32194978 MeRIP-seq:(Medium) rs767362471 Functional Loss SNV dbSNP153 33..33 33 - - - 76875 RMVar_ID_76875 Human_SNP_ID_171568794 m1A Human chr4 + 5051639 5051639 5051639 CTGCGAGCGCAGCCCGAGGCGGGGCACGGCGGAAGGCGCGGCGAGAGCGGGGTCCCTGCGAGCGC CTGCGAGCGCAGCCCGAGGCGGGGCACGGCGGGAGGCGCGGCGAGAGCGGGGTCCCTGCGAGCGC A G STK32B Ensembl:ENSG00000152953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:5051495..5051814 26863196 MeRIP-seq:(Medium) rs1190874917 Functional Loss SNV dbSNP153 33..33 33 - - - 76876 RMVar_ID_76876 Human_SNP_ID_171706973 m1A Human chr4 + 5499051 5499049 5499051 AGCTCCAGGACGGGTGCAACAACAACCTCCTCACCCACACCTGCACCCGTGGCTGCAGCAGCTGA AGCTCCAGGACGGGTGCAACAACAACCTCCT__CCCACACCTGCACCCGTGGCTGCAGCAGCTGA TCA T STK32B Ensembl:ENSG00000152953 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:5499003..5499102 26863196 MeRIP-seq:(Medium) rs1462595826 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_224601 76877 RMVar_ID_76877 Human_SNP_ID_171706977 m1A Human chr4 + 5499051 5499051 5499051 AGCTCCAGGACGGGTGCAACAACAACCTCCTCACCCACACCTGCACCCGTGGCTGCAGCAGCTGA AGCTCCAGGACGGGTGCAACAACAACCTCCTCGCCCACACCTGCACCCGTGGCTGCAGCAGCTGA A G STK32B Ensembl:ENSG00000152953 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:5499003..5499102 26863196 MeRIP-seq:(Medium) rs980460562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224601 76878 RMVar_ID_76878 Human_SNP_ID_171769310 m1A Human chr4 + 5711244 5711242 5711244 AAGCAGGGAAGGGGAGAGAAGCAGGAGTCGGGAGACTGCACAGGCCAGAAAGTCTGCGGAGCGGG AAGCAGGGAAGGGGAGAGAAGCAGGAGTCGG__GACTGCACAGGCCAGAAAGTCTGCGGAGCGGG GGA G EVC Ensembl:ENSG00000072840 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:5711241..5711356 26863196 MeRIP-seq:(Medium) rs886059494 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_353 76879 RMVar_ID_76879 Human_SNP_ID_171769339 m1A Human chr4 + 5711304 5711304 5711304 GCGGGCCGCGCCCCTGGCCCGCCCGGGCTCCAAGTCCCGCGTCGCCGCCCTGGCGGGGACGGTGC GCGGGCCGCGCCCCTGGCCCGCCCGGGCTCCACGTCCCGCGTCGCCGCCCTGGCGGGGACGGTGC A C EVC Ensembl:ENSG00000072840 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:5711236..5711373 26863196 MeRIP-seq:(Medium) rs1252062983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4787411,Human_RBP_ID_5531193 76880 RMVar_ID_76880 Human_SNP_ID_171797056 m1A Human chr4 - 5798683 5798683 5798683 CGCACTCCATGTGCTGCTGCAGAAGCTGCCCCACCTCCTGGGCCTCGGCCAGGAGCCGCTGCTGG CGCACTCCATGTGCTGCTGCAGAAGCTGCCCCCCCTCCTGGGCCTCGGCCAGGAGCCGCTGCTGG T G CRMP1 Ensembl:ENSG00000072832 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:5798555..5798741 26863196 MeRIP-seq:(Medium) rs1482763088 Functional Loss SNV dbSNP153 33..33 33 - - - 76881 RMVar_ID_76881 Human_SNP_ID_171797599 m1A Human chr4 + 5800489 5800489 5800489 GTGCCAGTGGGTACGGGGAGACTGGCCAGAAAAAAACTGAGGAGGAGGAGAGAAGGGGTGGCCAA GTGCCAGTGGGTACGGGGAGACTGGCCAGAAAGAAACTGAGGAGGAGGAGAGAAGGGGTGGCCAA A G EVC Ensembl:ENSG00000072840 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:5800486..5800776 26863196 MeRIP-seq:(Medium) rs1322746320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15840,RMVar_hsa_circ_91277,RMVar_hsa_circ_81851,RMVar_hsa_circ_224619,RMVar_hsa_circ_224625,RMVar_hsa_circ_28583,RMVar_hsa_circ_24260,RMVar_hsa_circ_224629 76882 RMVar_ID_76882 Human_SNP_ID_171811564 m1A Human chr4 + 5842616 5842616 5842616 ACTCACACACTCTCTCACACACACACACACACACTCACTCACACACACACACACGCACTGTCTCT ACTCACACACTCTCTCACACACACACACACACTCTCACTCACACACACACACACGCACTGTCTCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:5842547..5842632 26863196 MeRIP-seq:(Medium) rs372509657 Functional Loss SNV dbSNP153 33..33 33 - - - 76883 RMVar_ID_76883 Human_SNP_ID_171929215 m1A Human chr4 - 6269915 6269915 6269915 TCGGGAGCAGCTGAACGCGGCGCAAACGGGAGATCTGCGGCCGCGGGGGAGCAATCTGCACTCGC TCGGGAGCAGCTGAACGCGGCGCAAACGGGAGGTCTGCGGCCGCGGGGGAGCAATCTGCACTCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6269866..6270062 26863196 MeRIP-seq:(Medium) rs886059523 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_354 76884 RMVar_ID_76884 Human_SNP_ID_171929216 m1A Human chr4 - 6269915 6269915 6269915 TCGGGAGCAGCTGAACGCGGCGCAAACGGGAGATCTGCGGCCGCGGGGGAGCAATCTGCACTCGC TCGGGAGCAGCTGAACGCGGCGCAAACGGGAGCTCTGCGGCCGCGGGGGAGCAATCTGCACTCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6269866..6270062 26863196 MeRIP-seq:(Medium) rs886059523 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_354 76885 RMVar_ID_76885 Human_SNP_ID_172038042 m1A Human chr4 + 6641020 6641020 6641020 GACGCGCGAGCACGGGCGGGCGTACCTGCGGAACCGGAGCAAGCTGTGGGAGATGGACAATATGC GACGCGCGAGCACGGGCGGGCGTACCTGCGGACCCGGAGCAAGCTGTGGGAGATGGACAATATGC A C MRFAP1 Ensembl:ENSG00000179010 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:6640778..6641320 32194978 MeRIP-seq:(Medium) rs761381560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622905,Human_RBP_ID_1639659,Human_RBP_ID_1980113,Human_RBP_ID_4788392,Human_RBP_ID_7321254,Human_RBP_ID_8593643,Human_RBP_ID_9396175,Human_RBP_ID_15182671,Human_RBP_ID_22457648,Human_RBP_ID_23136090,Human_RBP_ID_24060841,Human_RBP_ID_27328008,Human_RBP_ID_27508923 Human_miRNA_ID_2867372,Human_miRNA_ID_3002516 RMVar_hsa_circ_117309,RMVar_hsa_circ_224683,RMVar_hsa_circ_224682 76886 RMVar_ID_76886 Human_SNP_ID_172038087 m1A Human chr4 + 6641112 6641112 6641112 CCTCGGAGGAGAGCGCCCTCAACCACCTCCAGAACCCGGGCGACGCGGCCGAGGGCCGGGCGGCC CCTCGGAGGAGAGCGCCCTCAACCACCTCCAGGACCCGGGCGACGCGGCCGAGGGCCGGGCGGCC A G MRFAP1 Ensembl:ENSG00000179010 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:6640726..6641275 26863196 MeRIP-seq:(Medium) rs1220145697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249203,Human_RBP_ID_622909,Human_RBP_ID_4788402,Human_RBP_ID_22457839,Human_RBP_ID_26349159,Human_RBP_ID_27069118,Human_RBP_ID_27328010 Human_miRNA_ID_1548213,Human_miRNA_ID_2791931 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76887 RMVar_ID_76887 Human_SNP_ID_172038130 m1A Human chr4 + 6641167 6641167 6641167 CCGGGCGGCCAAGAGGTGCGAGAAGGCCGAGGAGAAGGCCAAGGAGATTGCGAAGATGGCAGAGA CCGGGCGGCCAAGAGGTGCGAGAAGGCCGAGGGGAAGGCCAAGGAGATTGCGAAGATGGCAGAGA A G MRFAP1 Ensembl:ENSG00000179010 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1016548821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622910,Human_RBP_ID_1639661,Human_RBP_ID_4800093,Human_RBP_ID_18032260,Human_RBP_ID_22458541,Human_RBP_ID_24060843,Human_RBP_ID_26349159,Human_RBP_ID_26771432,Human_RBP_ID_27069120 Human_Splice_Rec_543873,Human_Splice_Rec_543875,Human_Splice_Rec_543879,Human_Splice_Rec_543881 Human_miRNA_ID_2217148 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76888 RMVar_ID_76888 Human_SNP_ID_172038136 m1A Human chr4 + 6641176 6641176 6641176 CAAGAGGTGCGAGAAGGCCGAGGAGAAGGCCAAGGAGATTGCGAAGATGGCAGAGATGCTGGTGG CAAGAGGTGCGAGAAGGCCGAGGAGAAGGCCAGGGAGATTGCGAAGATGGCAGAGATGCTGGTGG A G MRFAP1 Ensembl:ENSG00000179010 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:6641126..6641175 26863196 MeRIP-seq:(Medium) rs776194851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622910,Human_RBP_ID_1639661,Human_RBP_ID_9396176,Human_RBP_ID_18032260,Human_RBP_ID_22458541,Human_RBP_ID_24060843,Human_RBP_ID_26349159,Human_RBP_ID_26771432 Human_Splice_Rec_543873,Human_Splice_Rec_543875,Human_Splice_Rec_543879,Human_Splice_Rec_543881 Human_miRNA_ID_2217148 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76889 RMVar_ID_76889 Human_SNP_ID_172038162 m1A Human chr4 + 6641229 6641229 6641229 AGATGCTGGTGGAGCTGGTCCGGCGGATAGAGAAGAGCGAGTCGTCGTGAGCGCGGTCGGCGGTA AGATGCTGGTGGAGCTGGTCCGGCGGATAGAGGAGAGCGAGTCGTCGTGAGCGCGGTCGGCGGTA A G MRFAP1 Ensembl:ENSG00000179010 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:6641132..6641248 26863196 MeRIP-seq:(Medium) rs866289712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249204,Human_RBP_ID_786363,Human_RBP_ID_1036939,Human_RBP_ID_1980114,Human_RBP_ID_4788409,Human_RBP_ID_5212533,Human_RBP_ID_7321259,Human_RBP_ID_8593645,Human_RBP_ID_9334623,Human_RBP_ID_9396176,Human_RBP_ID_15182676,Human_RBP_ID_17662065,Human_RBP_ID_18028346,Human_RBP_ID_19014325,Human_RBP_ID_22094747,Human_RBP_ID_22457650,Human_RBP_ID_24060843,Human_RBP_ID_26348878,Human_RBP_ID_26771330 Human_Splice_Rec_543873,Human_Splice_Rec_543875,Human_Splice_Rec_543879,Human_Splice_Rec_543881 Human_miRNA_ID_3116471 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76890 RMVar_ID_76890 Human_SNP_ID_172038351 m1A Human chr4 + 6641755 6641755 6641755 GCTTTAGGTTTCCAGCCAATGGATTCTGGTCAACTGGTGGAGATTGGCTGACACCCTGGAGAAGC GCTTTAGGTTTCCAGCCAATGGATTCTGGTCAGCTGGTGGAGATTGGCTGACACCCTGGAGAAGC A G MRFAP1 Ensembl:ENSG00000179010 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:6641715..6641843;chr4:6641726..6642030;chr4:6641726..6641975 26863196 MeRIP-seq:(Medium) rs1480122030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622913,Human_RBP_ID_1036941,Human_RBP_ID_1639665,Human_RBP_ID_1980116,Human_RBP_ID_3742086,Human_RBP_ID_4800096,Human_RBP_ID_5150599,Human_RBP_ID_9162175,Human_RBP_ID_15182683,Human_RBP_ID_17295075,Human_RBP_ID_17408581,Human_RBP_ID_17524638,Human_RBP_ID_17662200,Human_RBP_ID_18032261,Human_RBP_ID_18348617,Human_RBP_ID_22457841,Human_RBP_ID_22510842,Human_RBP_ID_23136092,Human_RBP_ID_24060851 Human_Splice_Rec_543874,Human_Splice_Rec_543876,Human_Splice_Rec_543880,Human_Splice_Rec_543882 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76891 RMVar_ID_76891 Human_SNP_ID_172038368 m1A Human chr4 + 6641797 6641797 6641797 ATTGGCTGACACCCTGGAGAAGCCGAAACCAGAGAGCCTTTTGTTTTCTCTTTTTTCCTGTCTAT ATTGGCTGACACCCTGGAGAAGCCGAAACCAGGGAGCCTTTTGTTTTCTCTTTTTTCCTGTCTAT A G MRFAP1 Ensembl:ENSG00000179010 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:6641776..6641800 26863196 MeRIP-seq:(Medium) rs1172663759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622914,Human_RBP_ID_1317456,Human_RBP_ID_1639666,Human_RBP_ID_1980117,Human_RBP_ID_2853854,Human_RBP_ID_3742086,Human_RBP_ID_4788414,Human_RBP_ID_7321263,Human_RBP_ID_8593649,Human_RBP_ID_17524640,Human_RBP_ID_17662200,Human_RBP_ID_21058111,Human_RBP_ID_24060853,Human_RBP_ID_24430305,Human_RBP_ID_24502390 Human_Splice_Rec_543874,Human_Splice_Rec_543876,Human_Splice_Rec_543880,Human_Splice_Rec_543882 Human_miRNA_ID_937148,Human_miRNA_ID_957250,Human_miRNA_ID_1763941 RMVar_hsa_circ_117309,RMVar_hsa_circ_224682,RMVar_hsa_circ_224684 76892 RMVar_ID_76892 Human_SNP_ID_172043002 m1A Human chr4 + 6658962 6658962 6658962 TGGGCAGGCGGATCGTGGAGCTGCACCAGCGGATCGCCGGCTGCGAGTGCTGCCGAGCCGGCGGG TGGGCAGGCGGATCGTGGAGCTGCACCAGCGGCTCGCCGGCTGCGAGTGCTGCCGAGCCGGCGGG A C AC093323.4 Ensembl:ENSG00000284847 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:6658879..6659008 26863410 MeRIP-seq:(Medium) rs1398214963 Functional Loss SNV dbSNP153 33..33 33 - - - 76893 RMVar_ID_76893 Human_SNP_ID_172048385 m1A Human chr4 + 6674496 6674496 6674496 GGTGGCTCGGCTGTGCGCCGAAGCAGAGAGGAAGGCTGCGGAGGCGGCGCGGATGGGCAGGCGGA GGTGGCTCGGCTGTGCGCCGAAGCAGAGAGGAGGGCTGCGGAGGCGGCGCGGATGGGCAGGCGGA A G AC093323.1 Ensembl:ENSG00000170846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6673990..6674700 26863196 MeRIP-seq:(Medium) rs552535423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4788490,Human_RBP_ID_22095416 76894 RMVar_ID_76894 Human_SNP_ID_172048388 m1A Human chr4 - 6674500 6674500 6674500 ACGATCCGCCTGCCCATCCGCGCCGCCTCCGCAGCCTTCCTCTCTGCTTCGGCGCACAGCCGAGC ACGATCCGCCTGCCCATCCGCGCCGCCTCCGCGGCCTTCCTCTCTGCTTCGGCGCACAGCCGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:6674056..6674700;chr4:6674389..6674602;chr4:6674076..6674749;chr4:6674010..6674700 26863196 MeRIP-seq:(Medium) rs1011886688 Functional Loss SNV dbSNP153 33..33 33 - - - 76895 RMVar_ID_76895 Human_SNP_ID_172048598 m1A Human chr4 + 6674952 6674952 6674952 TGACTCCCGGATATGAGAATATCAAGCTCAAAATTTATGTTGTGATGATGAATTTCTCCCACTTG TGACTCCCGGATATGAGAATATCAAGCTCAAAGTTTATGTTGTGATGATGAATTTCTCCCACTTG A G AC093323.1 Ensembl:ENSG00000170846 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:6674948..6675148 32194978 MeRIP-seq:(Medium) rs1023790299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1036967,Human_RBP_ID_1980139,Human_RBP_ID_24071891 76896 RMVar_ID_76896 Human_SNP_ID_172054058 m1A Human chr4 - 6693943 6693943 6693943 AGACGTCTATGATCATGCCCATGGCTGTCTCTAGTTCCGTCATGGTGCTAGATTCAGACCCACCT AGACGTCTATGATCATGCCCATGGCTGTCTCTGGTTCCGTCATGGTGCTAGATTCAGACCCACCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6693851..6694234 26863196 MeRIP-seq:(Medium) rs1167297452 Functional Loss SNV dbSNP153 33..33 33 - - - 76897 RMVar_ID_76897 Human_SNP_ID_172054060 m1A Human chr4 + 6693950 6693950 6693950 TCTGAATCTAGCACCATGACGGAACTAGAGACAGCCATGGGCATGATCATAGACGTCTTTTCCCG TCTGAATCTAGCACCATGACGGAACTAGAGACGGCCATGGGCATGATCATAGACGTCTTTTCCCG A G S100P Ensembl:ENSG00000163993 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:6693901..6693975 26863196 MeRIP-seq:(Medium) rs1458743676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794860,Human_RBP_ID_5607464,Human_RBP_ID_17662203,Human_RBP_ID_18424549 RMVar_hsa_circ_119418,RMVar_hsa_circ_224687 76898 RMVar_ID_76898 Human_SNP_ID_172054863 m1A Human chr4 - 6696847 6696847 6696847 AGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCAGGGCCTCAGCCTCCACCAAGCACTGCTGCTGG AGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCTGGGCCTCAGCCTCCACCAAGCACTGCTGCTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:6696842..6697106 26863196 MeRIP-seq:(Medium) rs760432220 Functional Loss SNV dbSNP153 33..33 33 - - - 76899 RMVar_ID_76899 Human_SNP_ID_172054864 m1A Human chr4 - 6696847 6696847 6696847 AGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCAGGGCCTCAGCCTCCACCAAGCACTGCTGCTGG AGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCCGGGCCTCAGCCTCCACCAAGCACTGCTGCTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:6696842..6697106 26863196 MeRIP-seq:(Medium) rs760432220 Functional Loss SNV dbSNP153 33..33 33 - - - 76900 RMVar_ID_76900 Human_SNP_ID_172054878 m1A Human chr4 - 6696879 6696877 6696879 CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CATCCTTGTCTTTTCCACTCTAGAGGAGAGAG__GCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6696876..6696925 26863196 MeRIP-seq:(Medium) rs753257885 Functional Loss DEL dbSNP153 33..34 33 - - - 76901 RMVar_ID_76901 Human_SNP_ID_172054883 m1A Human chr4 - 6696879 6696879 6696879 CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGGGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6696876..6696925 26863196 MeRIP-seq:(Medium) rs757583212 Functional Loss SNV dbSNP153 33..33 33 - - - 76902 RMVar_ID_76902 Human_SNP_ID_172054884 m1A Human chr4 - 6696879 6696879 6696879 CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGCGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6696876..6696925 26863196 MeRIP-seq:(Medium) rs757583212 Functional Loss SNV dbSNP153 33..33 33 - - - 76903 RMVar_ID_76903 Human_SNP_ID_172058400 m1A Human chr4 + 6709341 6709341 6709341 AATCTCCTTGGCTTTCTCCTCAGCCTTCTCGCACAACTCCGACACTCTCTCGTCGGCTTCGCCAC AATCTCCTTGGCTTTCTCCTCAGCCTTCTCGCGCAACTCCGACACTCTCTCGTCGGCTTCGCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:6709226..6709820;chr4:6709226..6709875 26863196 MeRIP-seq:(Medium) rs759990042 Functional Loss SNV dbSNP153 33..33 33 - - - 76904 RMVar_ID_76904 Human_SNP_ID_172060265 m1A Human chr4 - 6716211 6716211 6716211 GCAGCGCTCCGCCATCCGAAAAGCTACCCTCCATGGCCCGCGACCACCCGACTGCGCAGCGCTCG GCAGCGCTCCGCCATCCGAAAAGCTACCCTCCGTGGCCCGCGACCACCCGACTGCGCAGCGCTCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6716101..6716770 26863196 MeRIP-seq:(Medium) rs1315138550 Functional Loss SNV dbSNP153 33..33 33 - - - 76905 RMVar_ID_76905 Human_SNP_ID_172060267 m1A Human chr4 + 6716214 6716214 6716214 GCGCTGCGCAGTCGGGTGGTCGCGGGCCATGGAGGGTAGCTTTTCGGATGGCGGAGCGCTGCCGG GCGCTGCGCAGTCGGGTGGTCGCGGGCCATGGTGGGTAGCTTTTCGGATGGCGGAGCGCTGCCGG A T BLOC1S4 Ensembl:ENSG00000186222 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr4:6716163..6716407;chr4:6716098..6716475 26863196 MeRIP-seq:(Medium) rs1405095604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794862,Human_RBP_ID_5475650,Human_RBP_ID_22292612,Human_RBP_ID_23120124,Human_RBP_ID_27069262 76906 RMVar_ID_76906 Human_SNP_ID_172060272 m1A Human chr4 - 6716222 6716221 6716222 GAGCCCCTCCGGCAGCGCTCCGCCATCCGAAAAGCTACCCTCCATGGCCCGCGACCACCCGACTG GAGCCCCTCCGGCAGCGCTCCGCCATCCGAAA_GCTACCCTCCATGGCCCGCGACCACCCGACTG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr4:6716125..6716459;chr4:6716158..6716337 26863196 MeRIP-seq:(Medium) rs1313912201 Functional Loss DEL dbSNP153 33..33 33 - - - 76907 RMVar_ID_76907 Human_SNP_ID_172060274 m1A Human chr4 - 6716222 6716222 6716222 GAGCCCCTCCGGCAGCGCTCCGCCATCCGAAAAGCTACCCTCCATGGCCCGCGACCACCCGACTG GAGCCCCTCCGGCAGCGCTCCGCCATCCGAAATGCTACCCTCCATGGCCCGCGACCACCCGACTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr4:6716125..6716459;chr4:6716158..6716337 26863196 MeRIP-seq:(Medium) rs1182946038 Functional Loss SNV dbSNP153 33..33 33 - - - 76908 RMVar_ID_76908 Human_SNP_ID_172060525 m1A Human chr4 + 6716678 6716678 6716678 GGGGCCGCGTGGCCAGGATGGAGGAGCAGGTCACCAAGGCCGAGGCCGAGCTGGGCACCTTCCCC GGGGCCGCGTGGCCAGGATGGAGGAGCAGGTCCCCAAGGCCGAGGCCGAGCTGGGCACCTTCCCC A C BLOC1S4 Ensembl:ENSG00000186222 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:6716544..6716790 32194978 MeRIP-seq:(Medium) rs981214962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27069268 76909 RMVar_ID_76909 Human_SNP_ID_172076254 m1A Human chr4 - 6765488 6765488 6765488 ATGACCTTCAAGCCCTTCGCTCTCTGACTGCTACTGCCCCAGCCGACATCCCCCAGGCTTCTCTC ATGACCTTCAAGCCCTTCGCTCTCTGACTGCTTCTGCCCCAGCCGACATCCCCCAGGCTTCTCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6765462..6765596 26863196 MeRIP-seq:(Medium) rs1239958498 Functional Loss SNV dbSNP153 33..33 33 - - - 76910 RMVar_ID_76910 Human_SNP_ID_172081458 m1A Human chr4 + 6782792 6782792 6782792 CGCTCGGCAGCCGCCCGCAGCCCCTCGGAGCCAGAGGAGAGGCGCCCCCGCCGGCCGCCGCGCCG CGCTCGGCAGCCGCCCGCAGCCCCTCGGAGCCTGAGGAGAGGCGCCCCCGCCGGCCGCCGCGCCG A T KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr4:6782744..6783007;chr4:6782741..6783176 26863196 MeRIP-seq:(Medium) rs1161899586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4788683,Human_RBP_ID_18424726 Human_Splice_Rec_543929,Human_Splice_Rec_543931,Human_Splice_Rec_543949 76911 RMVar_ID_76911 Human_SNP_ID_172081808 m1A Human chr4 + 6783601 6783601 6783601 CCAGCATTGTCCTTTTGGGGCCCCGGGAAGGGAAAACCGCCGGGCGGGGGAGGAGGGCCGCAGGC CCAGCATTGTCCTTTTGGGGCCCCGGGAAGGGGAAACCGCCGGGCGGGGGAGGAGGGCCGCAGGC A G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:6783593..6783745 26863196 MeRIP-seq:(Medium) rs951296578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3747313,Human_RBP_ID_5089918,Human_RBP_ID_8129871 76912 RMVar_ID_76912 Human_SNP_ID_172085452 m1A Human chr4 + 6795968 6795968 6795968 AAGGCACTGGTGGAGGAAGCGAATGGAAATAGAGAAGTCCAAGGGCAGAGCCTGGAAAGCTGGGA AAGGCACTGGTGGAGGAAGCGAATGGAAATAGGGAAGTCCAAGGGCAGAGCCTGGAAAGCTGGGA A G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6795953..6796133 26863196 MeRIP-seq:(Medium) rs983543995 Functional Loss SNV dbSNP153 33..33 33 - - - 76913 RMVar_ID_76913 Human_SNP_ID_172085455 m1A Human chr4 + 6795976 6795976 6795976 GGTGGAGGAAGCGAATGGAAATAGAGAAGTCCAAGGGCAGAGCCTGGAAAGCTGGGAAGAGGAGG GGTGGAGGAAGCGAATGGAAATAGAGAAGTCCGAGGGCAGAGCCTGGAAAGCTGGGAAGAGGAGG A G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:6795952..6796024 26863196 MeRIP-seq:(Medium) rs992839624 Functional Loss SNV dbSNP153 33..33 33 - - - 76914 RMVar_ID_76914 Human_SNP_ID_172103667 m1A Human chr4 - 6861347 6861347 6861347 TGCTTTGCCCATTCCGCCCTTTTTTGTTTCGAATCTCTCGTGCCTTGTGTCTTACTTTAACATAC TGCTTTGCCCATTCCGCCCTTTTTTGTTTCGAGTCTCTCGTGCCTTGTGTCTTACTTTAACATAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6861298..6861486 26863196 MeRIP-seq:(Medium) rs1560199907 Functional Loss SNV dbSNP153 33..33 33 - - - 76915 RMVar_ID_76915 Human_SNP_ID_172106735 m1A Human chr4 - 6872401 6872390 6872402 CCACTCCTGTCTCCCTCTCTACCTAGACTCCCATAACTACTCCTCATAGAAAGTAATCCAACAAA CCACTCCTGTCTCCCTCTCTACCTAGACTCC____________TCATAGAAAGTAATCCAACAAA AGGAGTAGTTATG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6872370..6872482 26863196 MeRIP-seq:(Medium) rs1276635702 Functional Loss DEL dbSNP153 32..43 33 - - - 76916 RMVar_ID_76916 Human_SNP_ID_172123381 m1A Human chr4 - 6929364 6929364 6929364 ACAGTAGAGGGACTGACCCAGTGGCCTCCAGCACTAGTCTGCCCACCTTCGAATCTTCTTGCTTC ACAGTAGAGGGACTGACCCAGTGGCCTCCAGCTCTAGTCTGCCCACCTTCGAATCTTCTTGCTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:6929352..6929417 26863196 MeRIP-seq:(Medium) rs1369297625 Functional Loss SNV dbSNP153 33..33 33 - - - 76917 RMVar_ID_76917 Human_SNP_ID_172124064 m1A Human chr4 + 6931937 6931937 6931937 ACACAGTGAGTAGATGGAGGATATGTGTTGGCAGACTTAAGAGCTACGGAGAAAGCCAGCAAGCA ACACAGTGAGTAGATGGAGGATATGTGTTGGCGGACTTAAGAGCTACGGAGAAAGCCAGCAAGCA A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:6931919..6932083 26863196 MeRIP-seq:(Medium) rs978047767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15188208 RMVar_hsa_circ_125682,RMVar_hsa_circ_301538,RMVar_hsa_circ_321604,RMVar_hsa_circ_277280,RMVar_hsa_circ_128013,RMVar_hsa_circ_224702,RMVar_hsa_circ_224704,RMVar_hsa_circ_224706,RMVar_hsa_circ_94610,RMVar_hsa_circ_224705,RMVar_hsa_circ_224703,RMVar_hsa_circ_224701 76918 RMVar_ID_76918 Human_SNP_ID_172124065 m1A Human chr4 + 6931937 6931937 6931937 ACACAGTGAGTAGATGGAGGATATGTGTTGGCAGACTTAAGAGCTACGGAGAAAGCCAGCAAGCA ACACAGTGAGTAGATGGAGGATATGTGTTGGCTGACTTAAGAGCTACGGAGAAAGCCAGCAAGCA A T TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:6931919..6932083 26863196 MeRIP-seq:(Medium) rs978047767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15188208 RMVar_hsa_circ_125682,RMVar_hsa_circ_301538,RMVar_hsa_circ_321604,RMVar_hsa_circ_277280,RMVar_hsa_circ_128013,RMVar_hsa_circ_224702,RMVar_hsa_circ_224704,RMVar_hsa_circ_224706,RMVar_hsa_circ_94610,RMVar_hsa_circ_224705,RMVar_hsa_circ_224703,RMVar_hsa_circ_224701 76919 RMVar_ID_76919 Human_SNP_ID_172124696 m1A Human chr4 - 6933883 6933883 6933883 CTCCCTACAGCTGCCACCCAGGTGAAGCCATCATCACCTCTTGTCTGGACTCTTGCAACAGCCTC CTCCCTACAGCTGCCACCCAGGTGAAGCCATCGTCACCTCTTGTCTGGACTCTTGCAACAGCCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:6933881..6934344 26863196 MeRIP-seq:(Medium) rs1450470013 Functional Loss SNV dbSNP153 33..33 33 - - - 76920 RMVar_ID_76920 Human_SNP_ID_172124697 m1A Human chr4 - 6933883 6933883 6933883 CTCCCTACAGCTGCCACCCAGGTGAAGCCATCATCACCTCTTGTCTGGACTCTTGCAACAGCCTC CTCCCTACAGCTGCCACCCAGGTGAAGCCATCCTCACCTCTTGTCTGGACTCTTGCAACAGCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:6933881..6934344 26863196 MeRIP-seq:(Medium) rs1450470013 Functional Loss SNV dbSNP153 33..33 33 - - - 76921 RMVar_ID_76921 Human_SNP_ID_172138077 m1A Human chr4 + 6980323 6980323 6980323 CTAAATCATGGGCCCATGAGGAAGTCACAAGGAAAATTAGAAAATATTTTGAAGCGAACGAGAAC CTAAATCATGGGCCCATGAGGAAGTCACAAGGGAAATTAGAAAATATTTTGAAGCGAACGAGAAC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:6980310..6980394 26863196 MeRIP-seq:(Medium) rs549692562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125682,RMVar_hsa_circ_301538,RMVar_hsa_circ_321604,RMVar_hsa_circ_128013,RMVar_hsa_circ_224702,RMVar_hsa_circ_224704,RMVar_hsa_circ_94610,RMVar_hsa_circ_224705,RMVar_hsa_circ_224703,RMVar_hsa_circ_354634,RMVar_hsa_circ_362571,RMVar_hsa_circ_224701,RMVar_hsa_circ_356665,RMVar_hsa_circ_6800,RMVar_hsa_circ_323381,RMVar_hsa_circ_224709 76922 RMVar_ID_76922 Human_SNP_ID_172145918 m1A Human chr4 - 7007206 7007206 7007206 TCAGCTGCACTGCTCTCCTGGTCTACCTGCTCAGAAACCTGTCACCCCGGCTTGGCCACCCACCC TCAGCTGCACTGCTCTCCTGGTCTACCTGCTCCGAAACCTGTCACCCCGGCTTGGCCACCCACCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7007086..7007352 26863196 MeRIP-seq:(Medium) rs1304904850 Functional Loss SNV dbSNP153 33..33 33 - - - 76923 RMVar_ID_76923 Human_SNP_ID_172148221 m1A Human chr4 - 7015055 7015055 7015055 CTGCCCTTTACTTTCAACCTCTACCCCACCAGACCTGGCTACAGTGCCCGCTGACTCTGGAATGG CTGCCCTTTACTTTCAACCTCTACCCCACCAGGCCTGGCTACAGTGCCCGCTGACTCTGGAATGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7015049..7015366 26863196 MeRIP-seq:(Medium) rs566193849 Functional Loss SNV dbSNP153 33..33 33 - - - 76924 RMVar_ID_76924 Human_SNP_ID_172148232 m1A Human chr4 + 7015091 7015091 7015091 GTGGGGTAGAGGTTGAAAGTAAAGGGCAGAGGACGGCAGGCGATGAGGTGGGGAGGCCAGGTCAC GTGGGGTAGAGGTTGAAAGTAAAGGGCAGAGGGCGGCAGGCGATGAGGTGGGGAGGCCAGGTCAC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7015088..7015441 26863196 MeRIP-seq:(Medium) rs1361150710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54238,RMVar_hsa_circ_10947,RMVar_hsa_circ_337492,RMVar_hsa_circ_224730,RMVar_hsa_circ_224723,RMVar_hsa_circ_282236,RMVar_hsa_circ_365376 76925 RMVar_ID_76925 Human_SNP_ID_172156500 m1A Human chr4 - 7042100 7042017 7042101 TGACCGGGGCGCAGAGGCCGAGGCCCCCGAGAAAGAGCAAGCGTACCTGCGCCATCTGGGCATGC TGACCGGGGCGCAGAGGCCGAGGCCCCCGAG__________________________________ CCTGGTGGTACCACTGCAGGTCGTCTGCCTGCTGCTTCTTCAGCTCCTCCAGCATGCCCAGATGGCGCAGGTACGCTTGCTCTTT C AC097382.2,CCDC96 Ensembl:ENSG00000245748,Ensembl:ENSG00000173013 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7042023..7042123 26863196 MeRIP-seq:(Medium) rs1560388130 Functional Loss DEL dbSNP153 32..65 33 - - - 76926 RMVar_ID_76926 Human_SNP_ID_172156735 m1A Human chr4 - 7042451 7042451 7042451 AGAGGCTGCTGCAGCCCCGGAGGCCGAGACAGAGCGGGTGGAGGGGGAGGAAGAGGACAAGGAGG AGAGGCTGCTGCAGCCCCGGAGGCCGAGACAGGGCGGGTGGAGGGGGAGGAAGAGGACAAGGAGG T C AC097382.2,CCDC96 Ensembl:ENSG00000245748,Ensembl:ENSG00000173013 lincRNA,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7042291..7042861 26863196 MeRIP-seq:(Medium) rs1000346404 Functional Loss SNV dbSNP153 33..33 33 - - - 76927 RMVar_ID_76927 Human_SNP_ID_172156948 m1A Human chr4 - 7042790 7042790 7042790 ACCCGGGGAGCTGGAGTCGGAGCCGGAGGAGGAGGAGGAGGAGCAAGCGGCTTCGCAGGGAGGCA ACCCGGGGAGCTGGAGTCGGAGCCGGAGGAGGTGGAGGAGGAGCAAGCGGCTTCGCAGGGAGGCA T A AC097382.2,CCDC96 Ensembl:ENSG00000245748,Ensembl:ENSG00000173013 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7042288..7042915 26863196 MeRIP-seq:(Medium) rs1222988578 Functional Loss SNV dbSNP153 33..33 33 - - - 76928 RMVar_ID_76928 Human_SNP_ID_172157270 m1A Human chr4 - 7043446 7043446 7043446 AGCAACCGCCGCCCGCCGCCGCGGCTGCCGCCACCGCGGCCCCAGCCCAGCCGCCGCCAGAGCCA AGCAACCGCCGCCCGCCGCCGCGGCTGCCGCCGCCGCGGCCCCAGCCCAGCCGCCGCCAGAGCCA T C AC097382.2 Ensembl:ENSG00000245748 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:7043341..7043772 26863196 MeRIP-seq:(Medium) rs1423079594 Functional Loss SNV dbSNP153 33..33 33 - - - 76929 RMVar_ID_76929 Human_SNP_ID_172157306 m1A Human chr4 - 7043543 7043543 7043543 CCCCGCTCGCCGCCCGCCGCCCGGCCCGCCGCAGCCGCCGCGCCCCCGGCCGTCAGCGCCCCGCC CCCCGCTCGCCGCCCGCCGCCCGGCCCGCCGCCGCCGCCGCGCCCCCGGCCGTCAGCGCCCCGCC T G AC097382.2 Ensembl:ENSG00000245748 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:7043451..7043551 26863410 MeRIP-seq:(Medium) rs1268110063 Functional Loss SNV dbSNP153 33..33 33 - - - 76930 RMVar_ID_76930 Human_SNP_ID_172157320 m1A Human chr4 - 7043604 7043604 7043604 CAGCGGGCTCACCTCGGCCAGGCAGTACACGCAGTACTTCTTCCCCAGCTCCGCCATCTTCCCCC CAGCGGGCTCACCTCGGCCAGGCAGTACACGCTGTACTTCTTCCCCAGCTCCGCCATCTTCCCCC T A AC097382.2 Ensembl:ENSG00000245748 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7043338..7052874 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76931 RMVar_ID_76931 Human_SNP_ID_172157321 m1A Human chr4 - 7043604 7043604 7043604 CAGCGGGCTCACCTCGGCCAGGCAGTACACGCAGTACTTCTTCCCCAGCTCCGCCATCTTCCCCC CAGCGGGCTCACCTCGGCCAGGCAGTACACGCGGTACTTCTTCCCCAGCTCCGCCATCTTCCCCC T C AC097382.2 Ensembl:ENSG00000245748 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7043338..7052874 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 76932 RMVar_ID_76932 Human_SNP_ID_172157327 m1A Human chr4 + 7043623 7043623 7043623 GGGGAAGAAGTACTGCGTGTACTGCCTGGCCGAGGTGAGCCCGCTGCGCTTCCGCTGCACCGAGT GGGGAAGAAGTACTGCGTGTACTGCCTGGCCGTGGTGAGCCCGCTGCGCTTCCGCTGCACCGAGT A T TADA2B Ensembl:ENSG00000173011 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7043344..7052874 26863196 MeRIP-seq:(Medium) rs1468737162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249175,Human_RBP_ID_3747318,Human_RBP_ID_4794572,Human_RBP_ID_5242091 Human_Splice_Rec_544125 RMVar_hsa_circ_224731,RMVar_hsa_circ_125426 76933 RMVar_ID_76933 Human_SNP_ID_172160261 m1A Human chr4 + 7054078 7054078 7054078 CCCTTTGTCATCGTAGGAAGATATGGCTGCCCACGTTGGTGCTTCCCGGACTCCCCAAGAGGTGA CCCTTTGTCATCGTAGGAAGATATGGCTGCCCCCGTTGGTGCTTCCCGGACTCCCCAAGAGGTGA A C TADA2B Ensembl:ENSG00000173011 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7054060..7054318 26863196 MeRIP-seq:(Medium) rs760148474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940630,Human_RBP_ID_8880728 Human_Splice_Rec_544122,Human_Splice_Rec_544124,Human_Splice_Rec_544126,Human_Splice_Rec_544128 Human_miRNA_ID_2299655,Human_miRNA_ID_2302927,Human_miRNA_ID_2306190 RMVar_hsa_circ_224731,RMVar_hsa_circ_125426 76934 RMVar_ID_76934 Human_SNP_ID_172160294 m1A Human chr4 + 7054168 7054168 7054168 CCACGGGAACCTGGGGAAGGCCTGCATCCCCGACACCATCCCCAACCGCGTGACAGACCACACCT CCACGGGAACCTGGGGAAGGCCTGCATCCCCGCCACCATCCCCAACCGCGTGACAGACCACACCT A C TADA2B Ensembl:ENSG00000173011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:7054118..7054716 32194978 MeRIP-seq:(Medium) rs990820532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18825941,Human_RBP_ID_27509131 RMVar_hsa_circ_224731,RMVar_hsa_circ_125426 76935 RMVar_ID_76935 Human_SNP_ID_172160295 m1A Human chr4 + 7054168 7054168 7054168 CCACGGGAACCTGGGGAAGGCCTGCATCCCCGACACCATCCCCAACCGCGTGACAGACCACACCT CCACGGGAACCTGGGGAAGGCCTGCATCCCCGGCACCATCCCCAACCGCGTGACAGACCACACCT A G TADA2B Ensembl:ENSG00000173011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:7054118..7054716 32194978 MeRIP-seq:(Medium) rs990820532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18825941,Human_RBP_ID_27509131 RMVar_hsa_circ_224731,RMVar_hsa_circ_125426 76936 RMVar_ID_76936 Human_SNP_ID_172160922 m1A Human chr4 + 7056109 7056107 7056109 AGTGTCGCCAGGCCCGCGCCAGCTGAGGCCTCAGACTAGCCAGGCAAGAGCCGTCTGACCAGTTG AGTGTCGCCAGGCCCGCGCCAGCTGAGGCCT__GACTAGCCAGGCAAGAGCCGTCTGACCAGTTG TCA T TADA2B Ensembl:ENSG00000173011 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:7056059..7056259 32194978 MeRIP-seq:(Medium) rs1398868762 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_27328288 RMVar_hsa_circ_224731,RMVar_hsa_circ_125426 76937 RMVar_ID_76937 Human_SNP_ID_172162299 m1A Human chr4 - 7060751 7060751 7060751 TACGTGTGACCTTTTCCCAAACCTTATTGGAAACCTTAAGTAACCAGTGGCTAAACAGAAAAGCC TACGTGTGACCTTTTCCCAAACCTTATTGGAATCCTTAAGTAACCAGTGGCTAAACAGAAAAGCC T A GRPEL1 Ensembl:ENSG00000109519 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:7060701..7060750 32194978 MeRIP-seq:(Medium) rs373588098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623413,Human_RBP_ID_5120983,Human_RBP_ID_17295150,Human_RBP_ID_18028706,Human_RBP_ID_23213733,Human_RBP_ID_27069603 Human_miRNA_ID_1342635 RMVar_hsa_circ_93254,RMVar_hsa_circ_110200,RMVar_hsa_circ_224733,RMVar_hsa_circ_224734 76938 RMVar_ID_76938 Human_SNP_ID_172162845 m1A Human chr4 - 7062435 7062435 7062435 GGAAAAATATAAACGAGCTTTGGCAGACACTGAGAACTTACGGCAGAGGAGCCAGAAATTGGTGG GGAAAAATATAAACGAGCTTTGGCAGACACTGCGAACTTACGGCAGAGGAGCCAGAAATTGGTGG T G GRPEL1 Ensembl:ENSG00000109519 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:7062339..7062497;chr4:7062376..7062475;chr4:7062376..7062450 26863196 MeRIP-seq:(Medium) rs1339370044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1640032,Human_RBP_ID_1980381,Human_RBP_ID_2854807,Human_RBP_ID_7323228,Human_RBP_ID_15189128,Human_RBP_ID_18825959,Human_RBP_ID_27509195,Human_RBP_ID_27566976 Human_Splice_Rec_544132,Human_Splice_Rec_544133,Human_Splice_Rec_544138,Human_Splice_Rec_544140,Human_Splice_Rec_544141,Human_Splice_Rec_544146,Human_Splice_Rec_544147 Human_miRNA_ID_2082637 RMVar_hsa_circ_93254,RMVar_hsa_circ_110200,RMVar_hsa_circ_224733,RMVar_hsa_circ_224734 76939 RMVar_ID_76939 Human_SNP_ID_172163466 m1A Human chr4 - 7064173 7064173 7064173 GTGCACAGCCACGAAACAAAAGAACAGTGGCCAGAACCTGGAAGAGGACATGGGTCAGAGTGAAC GTGCACAGCCACGAAACAAAAGAACAGTGGCCGGAACCTGGAAGAGGACATGGGTCAGAGTGAAC T C GRPEL1 Ensembl:ENSG00000109519 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7064151..7064175 26863196 MeRIP-seq:(Medium) rs756000781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940633,Human_RBP_ID_1640034,Human_RBP_ID_1980383,Human_RBP_ID_3742532,Human_RBP_ID_4794867,Human_RBP_ID_5394737,Human_RBP_ID_8594092,Human_RBP_ID_15189150,Human_RBP_ID_24062359,Human_RBP_ID_26349172,Human_RBP_ID_26825331,Human_RBP_ID_27824670 Human_Splice_Rec_544130,Human_Splice_Rec_544136,Human_Splice_Rec_544144 Human_miRNA_ID_2570213,Human_miRNA_ID_2674386,Human_miRNA_ID_2925137 RMVar_hsa_circ_93254,RMVar_hsa_circ_110200,RMVar_hsa_circ_224733,RMVar_hsa_circ_224734 76940 RMVar_ID_76940 Human_SNP_ID_172164649 m1A Human chr4 + 7068016 7068016 7068016 CCAAAGCAGGAAGACTGCGCCGCGCCAACCTCACGCACTGAGCCGCCATGACTGCCACTGCCCGT CCAAAGCAGGAAGACTGCGCCGCGCCAACCTCCCGCACTGAGCCGCCATGACTGCCACTGCCCGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:7067929..7068075;chr4:7067906..7068050 26863196 MeRIP-seq:(Medium) rs1197725532 Functional Loss SNV dbSNP153 33..33 33 - - - 76941 RMVar_ID_76941 Human_SNP_ID_172200517 m1A Human chr4 - 7192603 7192603 7192603 GCGGCAGCGGAGCCGGCGGCGGGGCGGCGCGGACGAGGGGACCGCGGCCGGGAGAGCAGGAGGGC GCGGCAGCGGAGCCGGCGGCGGGGCGGCGCGGTCGAGGGGACCGCGGCCGGGAGAGCAGGAGGGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:7192559..7192767;chr4:7192566..7192660 26863196 MeRIP-seq:(Medium) rs535609144 Functional Loss SNV dbSNP153 33..33 33 - - - 76942 RMVar_ID_76942 Human_SNP_ID_172201881 m1A Human chr4 - 7197494 7197494 7197494 TCCATGCAGTCTTCCCTGATTTCCCCATCAGCATTATCGGGGGAGGGTGACACTTGCCCCCTCAT TCCATGCAGTCTTCCCTGATTTCCCCATCAGCGTTATCGGGGGAGGGTGACACTTGCCCCCTCAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7197445..7197531 26863196 MeRIP-seq:(Medium) rs12642071 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9232,GWAS_ID_9233 76943 RMVar_ID_76943 Human_SNP_ID_172263654 m1A Human chr4 - 7401145 7401145 7401145 CATCAATCCACTCATCCATCTGTCCATCTATCAGTCCATCCATCTATCCATCCATTCATCCACCC CATCAATCCACTCATCCATCTGTCCATCTATCGGTCCATCCATCTATCCATCCATTCATCCACCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7401142..7401354 26863196 MeRIP-seq:(Medium) rs1279610362 Functional Loss SNV dbSNP153 33..33 33 - - - 76944 RMVar_ID_76944 Human_SNP_ID_172263655 m1A Human chr4 - 7401145 7401145 7401145 CATCAATCCACTCATCCATCTGTCCATCTATCAGTCCATCCATCTATCCATCCATTCATCCACCC CATCAATCCACTCATCCATCTGTCCATCTATCCGTCCATCCATCTATCCATCCATTCATCCACCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7401142..7401354 26863196 MeRIP-seq:(Medium) rs1279610362 Functional Loss SNV dbSNP153 33..33 33 - - - 76945 RMVar_ID_76945 Human_SNP_ID_172308569 m1A Human chr4 - 7539668 7539668 7539668 CGGGGCCTCCATAACGGGGGTCGGGGCCTTGCAGCTGGGAAGGAGTTTGTAGGGCTGAAGGCAGG CGGGGCCTCCATAACGGGGGTCGGGGCCTTGCTGCTGGGAAGGAGTTTGTAGGGCTGAAGGCAGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7539537..7539681 26863196 MeRIP-seq:(Medium) rs903950506 Functional Loss SNV dbSNP153 33..33 33 - - - 76946 RMVar_ID_76946 Human_SNP_ID_172308570 m1A Human chr4 - 7539668 7539668 7539668 CGGGGCCTCCATAACGGGGGTCGGGGCCTTGCAGCTGGGAAGGAGTTTGTAGGGCTGAAGGCAGG CGGGGCCTCCATAACGGGGGTCGGGGCCTTGCGGCTGGGAAGGAGTTTGTAGGGCTGAAGGCAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7539537..7539681 26863196 MeRIP-seq:(Medium) rs903950506 Functional Loss SNV dbSNP153 33..33 33 - - - 76947 RMVar_ID_76947 Human_SNP_ID_172346412 m1A Human chr4 + 7657797 7657794 7657798 AGTGAGTGAGTCTGTGACTGGGTGAGTGAATGAGTGAGTGAGTGAATGAGTGAGTGGGTGAGTCT AGTGAGTGAGTCTGTGACTGGGTGAGTGAA____TGAGTGAGTGAATGAGTGAGTGGGTGAGTCT ATGAG A SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7657789..7657902 26863196 MeRIP-seq:(Medium) rs1025150892 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_14497,RMVar_hsa_circ_70708,RMVar_hsa_circ_368714,RMVar_hsa_circ_224737 76948 RMVar_ID_76948 Human_SNP_ID_172346444 m1A Human chr4 + 7657857 7657857 7657857 AGTCTGTGACTGAGTGAGTGAGTGAATGAGTAAGTGAATGAGTGAGTGAGTCACTGAGTGAATGA AGTCTGTGACTGAGTGAGTGAGTGAATGAGTACGTGAATGAGTGAGTGAGTCACTGAGTGAATGA A C SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7657653..7657930 26863196 MeRIP-seq:(Medium) rs910630863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14497,RMVar_hsa_circ_70708,RMVar_hsa_circ_368714,RMVar_hsa_circ_224737 76949 RMVar_ID_76949 Human_SNP_ID_172348073 m1A Human chr4 - 7663083 7663063 7663083 ATTCTCTCATTCACTTACTCATTCACTCACTCACTCACTCATTCACCCACTCTTTCACTCAATCA ATTCTCTCATTCACTTACTCATTCACTCACTC____________________TTTCACTCAATCA AGAGTGGGTGAATGAGTGAGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7663068..7663185 26863196 MeRIP-seq:(Medium) rs1181828929 Functional Loss DEL dbSNP153 33..52 33 - - - 76950 RMVar_ID_76950 Human_SNP_ID_172348084 m1A Human chr4 - 7663083 7663083 7663083 ATTCTCTCATTCACTTACTCATTCACTCACTCACTCACTCATTCACCCACTCTTTCACTCAATCA ATTCTCTCATTCACTTACTCATTCACTCACTCGCTCACTCATTCACCCACTCTTTCACTCAATCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7663068..7663185 26863196 MeRIP-seq:(Medium) rs1318786358 Functional Loss SNV dbSNP153 33..33 33 - - - 76951 RMVar_ID_76951 Human_SNP_ID_172348135 m1A Human chr4 - 7663205 7663197 7663205 TATTCACTCTTCACTCACTCATTCACTCACTCATTCACTCTTCACTCACTCACTCATTCACTCAT TATTCACTCTTCACTCACTCATTCACTCACTC________TTCACTCACTCACTCATTCACTCAT AGAGTGAAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7663089..7663295 26863196 MeRIP-seq:(Medium) rs1355862023 Functional Loss DEL dbSNP153 33..40 33 - - - 76952 RMVar_ID_76952 Human_SNP_ID_172352130 m1A Human chr4 + 7676267 7676267 7676267 TCCAGGGTGGATGTGGGCCAGGTCTGCCGCCGACCCCCTGCCCTCTGCCCTCTCACCCCACCTCT TCCAGGGTGGATGTGGGCCAGGTCTGCCGCCGCCCCCCTGCCCTCTGCCCTCTCACCCCACCTCT A C SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:7676090..7676279 26863196 MeRIP-seq:(Medium) rs1295073947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70708,RMVar_hsa_circ_48321,RMVar_hsa_circ_60757,RMVar_hsa_circ_327752,RMVar_hsa_circ_23378,RMVar_hsa_circ_224738,RMVar_hsa_circ_36958,RMVar_hsa_circ_224739 76953 RMVar_ID_76953 Human_SNP_ID_172381398 m1A Human chr4 + 7761851 7761851 7761851 TGGGAAGTGACCACTGGAGGGAGGGCTCCTCTATGGCAATGCAGCGGACGGCCCTGAGGTGTGTG TGGGAAGTGACCACTGGAGGGAGGGCTCCTCTGTGGCAATGCAGCGGACGGCCCTGAGGTGTGTG A G AFAP1-AS1 Ensembl:ENSG00000272620 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:7761826..7761850 32194978 MeRIP-seq:(Medium) rs1346585906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22726781 76954 RMVar_ID_76954 Human_SNP_ID_172386590 m1A Human chr4 - 7774839 7774839 7774839 GTAGAAGCAGATGCCAAGCGGCTACAGACCAAAGAGGAGGAGCTGCTGAAGAGGAAAGAGGCCCT GTAGAAGCAGATGCCAAGCGGCTACAGACCAAGGAGGAGGAGCTGCTGAAGAGGAAAGAGGCCCT T C AFAP1 Ensembl:ENSG00000196526 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7774688..7774935 26863196 MeRIP-seq:(Medium) rs754793929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941808 Human_Splice_Rec_544298,Human_Splice_Rec_544330,Human_Splice_Rec_544364,Human_Splice_Rec_544372,Human_Splice_Rec_544388,Human_Splice_Rec_544420 Human_miRNA_ID_246532,Human_miRNA_ID_249050,Human_miRNA_ID_3106523 RMVar_hsa_circ_5040,RMVar_hsa_circ_84246,RMVar_hsa_circ_88283,RMVar_hsa_circ_105115,RMVar_hsa_circ_224742,RMVar_hsa_circ_224743,RMVar_hsa_circ_297107,RMVar_hsa_circ_48254,RMVar_hsa_circ_82329,RMVar_hsa_circ_45455,RMVar_hsa_circ_31516,RMVar_hsa_circ_224746,RMVar_hsa_circ_224747,RMVar_hsa_circ_44079,RMVar_hsa_circ_224748,RMVar_hsa_circ_101279 76955 RMVar_ID_76955 Human_SNP_ID_172397948 m1A Human chr4 - 7809760 7809760 7809760 TGCTTTTTTGCTGTTGTTACTCTTGACAGTGAAGAGGAAGAAAAGTTCCAAATCAGAGGCCAAGG TGCTTTTTTGCTGTTGTTACTCTTGACAGTGAGGAGGAAGAAAAGTTCCAAATCAGAGGCCAAGG T C AFAP1 Ensembl:ENSG00000196526 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:7809710..7809807 26863196 MeRIP-seq:(Medium) rs751299100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941812 Human_Splice_Rec_544288,Human_Splice_Rec_544320,Human_Splice_Rec_544352,Human_Splice_Rec_544408,Human_Splice_Rec_544430 RMVar_hsa_circ_84246,RMVar_hsa_circ_105115,RMVar_hsa_circ_224743,RMVar_hsa_circ_82329,RMVar_hsa_circ_3467,RMVar_hsa_circ_224756,RMVar_hsa_circ_97678,RMVar_hsa_circ_31516,RMVar_hsa_circ_224746,RMVar_hsa_circ_224747,RMVar_hsa_circ_224748,RMVar_hsa_circ_101279,RMVar_hsa_circ_371503,RMVar_hsa_circ_116699,RMVar_hsa_circ_224749,RMVar_hsa_circ_224750,RMVar_hsa_circ_374508,RMVar_hsa_circ_224751,RMVar_hsa_circ_342172,RMVar_hsa_circ_335664,RMVar_hsa_circ_318146,RMVar_hsa_circ_224754,RMVar_hsa_circ_224755,RMVar_hsa_circ_224760,RMVar_hsa_circ_35492,RMVar_hsa_circ_308290,RMVar_hsa_circ_371145,RMVar_hsa_circ_113293,RMVar_hsa_circ_7330,RMVar_hsa_circ_224758,RMVar_hsa_circ_224759,RMVar_hsa_circ_224757,RMVar_hsa_circ_38345,RMVar_hsa_circ_300391,RMVar_hsa_circ_309257,RMVar_hsa_circ_48294,RMVar_hsa_circ_224762 76956 RMVar_ID_76956 Human_SNP_ID_172402258 m1A Human chr4 - 7823580 7823580 7823580 CTGTCTGCTAGAAAGTCGGAGCTGATGGGAACAGGAGAGGGATGGGGACACTCCAGGGACCAGGC CTGTCTGCTAGAAAGTCGGAGCTGATGGGAACCGGAGAGGGATGGGGACACTCCAGGGACCAGGC T G AFAP1 Ensembl:ENSG00000196526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7823572..7823666 26863196 MeRIP-seq:(Medium) rs1337750452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84246,RMVar_hsa_circ_105115,RMVar_hsa_circ_224743,RMVar_hsa_circ_224756,RMVar_hsa_circ_97678,RMVar_hsa_circ_31516,RMVar_hsa_circ_224747,RMVar_hsa_circ_224748,RMVar_hsa_circ_101279,RMVar_hsa_circ_371503,RMVar_hsa_circ_116699,RMVar_hsa_circ_224749,RMVar_hsa_circ_224750,RMVar_hsa_circ_374508,RMVar_hsa_circ_224751,RMVar_hsa_circ_335664,RMVar_hsa_circ_224755,RMVar_hsa_circ_35492,RMVar_hsa_circ_371145,RMVar_hsa_circ_113293,RMVar_hsa_circ_224758,RMVar_hsa_circ_224759,RMVar_hsa_circ_224757,RMVar_hsa_circ_224764,RMVar_hsa_circ_28154,RMVar_hsa_circ_38345,RMVar_hsa_circ_300391,RMVar_hsa_circ_309257,RMVar_hsa_circ_335259,RMVar_hsa_circ_224762,RMVar_hsa_circ_307939,RMVar_hsa_circ_43668,RMVar_hsa_circ_81862,RMVar_hsa_circ_111930,RMVar_hsa_circ_49653,RMVar_hsa_circ_224765 76957 RMVar_ID_76957 Human_SNP_ID_172415657 m1A Human chr4 + 7864119 7864119 7864119 CACAACCCATTCCCAACTTCCCATCACAACCCATTCCCAACTTCCCATCACAACACATTCCCAAC CACAACCCATTCCCAACTTCCCATCACAACCCCTTCCCAACTTCCCATCACAACACATTCCCAAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:7864096..7864168 26863196 MeRIP-seq:(Medium) rs80115971 Functional Loss SNV dbSNP153 33..33 33 - - - 76958 RMVar_ID_76958 Human_SNP_ID_172415666 m1A Human chr4 + 7864149 7864142 7864150 CCATTCCCAACTTCCCATCACAACACATTCCCAACTTCTCATCACAACCCACAGGTCCTTTGTAA CCATTCCCAACTTCCCATCACAACAC________CTTCTCATCACAACCCACAGGTCCTTTGTAA CATTCCCAA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:7863908..7864249 26863196 MeRIP-seq:(Medium) rs1405969112 Functional Loss DEL dbSNP153 27..34 33 - - - 76959 RMVar_ID_76959 Human_SNP_ID_172415671 m1A Human chr4 + 7864149 7864147 7864150 CCATTCCCAACTTCCCATCACAACACATTCCCAACTTCTCATCACAACCCACAGGTCCTTTGTAA CCATTCCCAACTTCCCATCACAACACATTCC___CTTCTCATCACAACCCACAGGTCCTTTGTAA CCAA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:7863908..7864249 26863196 MeRIP-seq:(Medium) rs1345772287 Functional Loss DEL dbSNP153 32..34 33 - - - 76960 RMVar_ID_76960 Human_SNP_ID_172421217 m1A Human chr4 + 7881289 7881289 7881289 TGCTGGCCCTCATGGGGTGACCCTCTGATAGCACCCGCCACTTGAGTCAAGGCTACCTCTCCTGC TGCTGGCCCTCATGGGGTGACCCTCTGATAGCCCCCGCCACTTGAGTCAAGGCTACCTCTCCTGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:7881243..7881407 26863196 MeRIP-seq:(Medium) rs1024015220 Functional Loss SNV dbSNP153 33..33 33 - - - 76961 RMVar_ID_76961 Human_SNP_ID_172422399 m1A Human chr4 + 7885274 7885272 7885274 ATGTGTCACACTTCAGGCCTTCTCAATCCCTCAGTTTCCCACAAATATCACGCCTGCTTCTGCCC ATGTGTCACACTTCAGGCCTTCTCAATCCCT__GTTTCCCACAAATATCACGCCTGCTTCTGCCC TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7885272..7885447 26863196 MeRIP-seq:(Medium) rs903864121 Functional Loss DEL dbSNP153 32..33 33 - - - 76962 RMVar_ID_76962 Human_SNP_ID_172425868 m1A Human chr4 - 7896411 7896411 7896411 GGGAGTAGGCAGAGGTGGGAGGAAGGAAGTCGAGAGTGATCAGACCCCTCGTTGGAGGTGCTTGC GGGAGTAGGCAGAGGTGGGAGGAAGGAAGTCGTGAGTGATCAGACCCCTCGTTGGAGGTGCTTGC T A AFAP1 Ensembl:ENSG00000196526 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7896409..7896563 26863196 MeRIP-seq:(Medium) rs1184684992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5211176 RMVar_hsa_circ_224775 76963 RMVar_ID_76963 Human_SNP_ID_172425955 m1A Human chr4 + 7896716 7896716 7896716 CACACACCCAGGGCTCAGTCCTCATTCCCCCCACACCCAGGGCTCAGTCCTCACTTCCCCACACC CACACACCCAGGGCTCAGTCCTCATTCCCCCCCCACCCAGGGCTCAGTCCTCACTTCCCCACACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7896659..7896925 26863196 MeRIP-seq:(Medium) rs1240480110 Functional Loss SNV dbSNP153 33..33 33 - - - 76964 RMVar_ID_76964 Human_SNP_ID_172438989 m1A Human chr4 + 7939251 7939251 7939251 GGTCCGCGCAGTCCCCTCGGTAAGTCGGACGAAGCAGTCTCGCTACGGGGGAGGGCGGCGGAGCC GGTCCGCGCAGTCCCCTCGGTAAGTCGGACGAGGCAGTCTCGCTACGGGGGAGGGCGGCGGAGCC A G AC097381.1 Ensembl:ENSG00000228919 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7939249..7939399 26863196 MeRIP-seq:(Medium) rs1398606132 Functional Loss SNV dbSNP153 33..33 33 - - - 76965 RMVar_ID_76965 Human_SNP_ID_172439255 m1A Human chr4 - 7939753 7939753 7939753 AGGCGGCGGCGGCGGCCCCGCCCCGGGGCTCCATTGTTAAGGCGGCTGCGGCTCTGTCGGCTGTT AGGCGGCGGCGGCGGCCCCGCCCCGGGGCTCCGTTGTTAAGGCGGCTGCGGCTCTGTCGGCTGTT T C AFAP1 Ensembl:ENSG00000196526 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7939703..7939825 26863196 MeRIP-seq:(Medium) rs1414426889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_544305,Human_Splice_Rec_544337 76966 RMVar_ID_76966 Human_SNP_ID_172439256 m1A Human chr4 + 7939756 7939756 7939756 AGCCGACAGAGCCGCAGCCGCCTTAACAATGGAGCCCCGGGGCGGGGCCGCCGCCGCCGCCTCAG AGCCGACAGAGCCGCAGCCGCCTTAACAATGGCGCCCCGGGGCGGGGCCGCCGCCGCCGCCTCAG A C AC097381.1 Ensembl:ENSG00000228919 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7939708..7939802 26863196 MeRIP-seq:(Medium) rs979390808 Functional Loss SNV dbSNP153 33..33 33 - - - 76967 RMVar_ID_76967 Human_SNP_ID_172448069 m1A Human chr4 + 7970489 7970489 7970489 TGCTGGAGGAGGGAGGAGTGGAGAGGGAGCGGATGGTGGGCAGGCGTGCCCCGCATGCTGGGGAA TGCTGGAGGAGGGAGGAGTGGAGAGGGAGCGGTTGGTGGGCAGGCGTGCCCCGCATGCTGGGGAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:7970477..7970595 26863196 MeRIP-seq:(Medium) rs775346683 Functional Loss SNV dbSNP153 33..33 33 - - - 76968 RMVar_ID_76968 Human_SNP_ID_172448656 m1A Human chr4 - 7972377 7972377 7972377 CTAGGAGGGCCTCCAGGAGGAGGGGACACTTGAGTCAGGACCAGTAGGATGACGAAGAGCTGCTG CTAGGAGGGCCTCCAGGAGGAGGGGACACTTGGGTCAGGACCAGTAGGATGACGAAGAGCTGCTG T C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:7972342..7972488 26863196 MeRIP-seq:(Medium) rs1254618655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224778 76969 RMVar_ID_76969 Human_SNP_ID_172448726 m1A Human chr4 - 7972666 7972666 7972666 AGGGGCCTCGTAGGCCAGGACAGTGGCGGGGGAGCCCCCGTGGCGCCACAGCAGAGAGCAGGACA AGGGGCCTCGTAGGCCAGGACAGTGGCGGGGGGGCCCCCGTGGCGCCACAGCAGAGAGCAGGACA T C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:7972617..7972745 26863196 MeRIP-seq:(Medium) rs921604677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224778 76970 RMVar_ID_76970 Human_SNP_ID_172448916 m1A Human chr4 - 7973159 7973159 7973159 GGCTCCTCCTGCCCCAGGGCCTTTGCACATGCACTTTATTCTTCCTGGAATTCCTTTCCTACTTG GGCTCCTCCTGCCCCAGGGCCTTTGCACATGCTCTTTATTCTTCCTGGAATTCCTTTCCTACTTG T A ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7973079..7973284 26863196 MeRIP-seq:(Medium) rs1323056981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224778 76971 RMVar_ID_76971 Human_SNP_ID_172465292 m1A Human chr4 - 8028430 8028426 8028430 GTGATTGAGTGAGCAAGTAAGTGAGTGAATGAATGAGTGAGTGAGTGAGTGAATGAGTGAATAAA GTGATTGAGTGAGCAAGTAAGTGAGTGAATGA____GTGAGTGAGTGAGTGAATGAGTGAATAAA CTCAT C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8028379..8028701 26863196 MeRIP-seq:(Medium) rs927789959 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_24066050 RMVar_hsa_circ_19001,RMVar_hsa_circ_56722 76972 RMVar_ID_76972 Human_SNP_ID_172486699 m1A Human chr4 - 8095064 8095056 8095064 AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGAAAGAGAAAGAAAGAAAGAAGGAAGGAAGGAAAG AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGA________GAAAGAAAGAAGGAAGGAAGGAAAG CTTTCTCTT C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8095045..8095112 26863196 MeRIP-seq:(Medium) rs553124573 Functional Loss DEL dbSNP153 33..40 33 - - - 76973 RMVar_ID_76973 Human_SNP_ID_172486706 m1A Human chr4 - 8095064 8095060 8095064 AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGAAAGAGAAAGAAAGAAAGAAGGAAGGAAGGAAAG AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGA____GAAAGAAAGAAAGAAGGAAGGAAGGAAAG CTCTT C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8095045..8095112 26863196 MeRIP-seq:(Medium) rs1243381928 Functional Loss DEL dbSNP153 33..36 33 - - - 76974 RMVar_ID_76974 Human_SNP_ID_172486710 m1A Human chr4 - 8095064 8095064 8095064 AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGAAAGAGAAAGAAAGAAAGAAGGAAGGAAGGAAAG AAGAAAGAAAGAGAGAGAGAGAGAAAGAAAGAGAGAGAAAGAAAGAAAGAAGGAAGGAAGGAAAG T C ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8095045..8095112 26863196 MeRIP-seq:(Medium) rs6816757 Functional Loss SNV dbSNP153 33..33 33 - - - 76975 RMVar_ID_76975 Human_SNP_ID_172505686 m1A Human chr4 - 8158790 8158790 8158790 CTGCCTGGCGTGTGCGCAAGGAGCGGGCGCGGAGCCGGCGGGCGGGCGGAGGATAGCGCGGGCGC CTGCCTGGCGTGTGCGCAAGGAGCGGGCGCGGGGCCGGCGGGCGGGCGGAGGATAGCGCGGGCGC T C ABLIM2 Ensembl:ENSG00000163995 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:8158618..8158834 26863196 MeRIP-seq:(Medium) rs1310887926 Functional Loss SNV dbSNP153 33..33 33 - - - 76976 RMVar_ID_76976 Human_SNP_ID_172505963 m1A Human chr4 - 8159493 8159493 8159493 GGCCCTGTGCTGGGCGCCTGATGTCACAGGGTAGCCGGTCACCGTGGAGGCTGGGGCCGGGGACT GGCCCTGTGCTGGGCGCCTGATGTCACAGGGTTGCCGGTCACCGTGGAGGCTGGGGCCGGGGACT T A lnc-ABLIM2-1 RNACentral:URS00008BA2C9 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8159386..8159748 26863196 MeRIP-seq:(Medium) rs1243466572 Functional Loss SNV dbSNP153 33..33 33 - - - 76977 RMVar_ID_76977 Human_SNP_ID_172505972 m1A Human chr4 + 8159518 8159518 8159518 GACCGGCTACCCTGTGACATCAGGCGCCCAGCACAGGGCCTGGACGCGGGTGCAGGAGAGGGAGT GACCGGCTACCCTGTGACATCAGGCGCCCAGCGCAGGGCCTGGACGCGGGTGCAGGAGAGGGAGT A G lnc-SH3TC1-3 RNACentral:URS0000D5AD3D lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8159471..8159674 32194978 MeRIP-seq:(Medium) rs1363759432 Functional Loss SNV dbSNP153 33..33 33 - - - 76978 RMVar_ID_76978 Human_SNP_ID_172505990 m1A Human chr4 + 8159598 8159598 8159598 AGCAGGGGTCCCCACTGTGTGCCTGGTGCGACAAAAGGCGAGCTGCAGAGAGGTCGGGAGGAGCC AGCAGGGGTCCCCACTGTGTGCCTGGTGCGACGAAAGGCGAGCTGCAGAGAGGTCGGGAGGAGCC A G lnc-SH3TC1-3 RNACentral:URS0000D5AD3D lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8159444..8159718 26863196 MeRIP-seq:(Medium) rs1456792137 Functional Loss SNV dbSNP153 33..33 33 - - - 76979 RMVar_ID_76979 Human_SNP_ID_172514591 m1A Human chr4 - 8189481 8189481 8189481 ACCCCCAATGCCTGCCCTGGCTTCTGCACACCACTCCTTCCTGGCACCCCTTCTCCTCCAGGCTG ACCCCCAATGCCTGCCCTGGCTTCTGCACACCGCTCCTTCCTGGCACCCCTTCTCCTCCAGGCTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:8189431..8189570 26863196 MeRIP-seq:(Medium) rs150852829 Functional Loss SNV dbSNP153 33..33 33 - - - 76980 RMVar_ID_76980 Human_SNP_ID_172514615 m1A Human chr4 - 8189591 8189591 8189591 TGACCCCTCTCTTTCCCCACCTGGTTACATCCAAGCCATCCTTGCCAGCCTCACCCTGCTCTCCC TGACCCCTCTCTTTCCCCACCTGGTTACATCCGAGCCATCCTTGCCAGCCTCACCCTGCTCTCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8189446..8190054 26863196 MeRIP-seq:(Medium) rs910322323 Functional Loss SNV dbSNP153 33..33 33 - - - 76981 RMVar_ID_76981 Human_SNP_ID_172519026 m1A Human chr4 + 8204866 8204866 8204866 AAAGAGGCAGTGACCGGCTCCTGAGGAGGGGCACAAGGCACCCAGGGGTTCTGCCTCGACAGGGA AAAGAGGCAGTGACCGGCTCCTGAGGAGGGGCGCAAGGCACCCAGGGGTTCTGCCTCGACAGGGA A G SH3TC1 Ensembl:ENSG00000125089 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8204860..8205007 26863196 MeRIP-seq:(Medium) rs1411487201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_544902 76982 RMVar_ID_76982 Human_SNP_ID_172526876 m1A Human chr4 + 8227970 8227970 8227970 GAACCTGGTGCTCCAGAACGCCCCCCAGCCCCACAGCCTCCCTGCCCAAACTTCCCACTACCTCA GAACCTGGTGCTCCAGAACGCCCCCCAGCCCCCCAGCCTCCCTGCCCAAACTTCCCACTACCTCA A C SH3TC1 Ensembl:ENSG00000125089 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8227919..8228018 26863196 MeRIP-seq:(Medium) rs780192982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27509572 Human_miRNA_ID_1036887,Human_miRNA_ID_1371338,Human_miRNA_ID_2028528,Human_miRNA_ID_2689068,Human_miRNA_ID_2692251,Human_miRNA_ID_2713077,Human_miRNA_ID_3049055 RMVar_hsa_circ_80135,RMVar_hsa_circ_104979,RMVar_hsa_circ_224785,RMVar_hsa_circ_88219,RMVar_hsa_circ_105322,RMVar_hsa_circ_224786,RMVar_hsa_circ_224787,RMVar_hsa_circ_224789,RMVar_hsa_circ_77571,RMVar_hsa_circ_224790 76983 RMVar_ID_76983 Human_SNP_ID_172526914 m1A Human chr4 + 8228023 8228023 8228023 CCCACTACCTCAGGCAAGCGCTGGCCTCCCTGACCCCGGGCACAGGCCAGGCGCTGCGCGGCCCC CCCACTACCTCAGGCAAGCGCTGGCCTCCCTGGCCCCGGGCACAGGCCAGGCGCTGCGCGGCCCC A G SH3TC1 Ensembl:ENSG00000125089 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8227894..8228073 26863196 MeRIP-seq:(Medium) rs753887862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22096242 RMVar_hsa_circ_80135,RMVar_hsa_circ_104979,RMVar_hsa_circ_224785,RMVar_hsa_circ_88219,RMVar_hsa_circ_105322,RMVar_hsa_circ_224786,RMVar_hsa_circ_224787,RMVar_hsa_circ_224789,RMVar_hsa_circ_77571,RMVar_hsa_circ_224790 76984 RMVar_ID_76984 Human_SNP_ID_172527097 m1A Human chr4 + 8228329 8228329 8228329 TGGTGGCCGTGGCTCTGAAGAGGACGGGCCGGACGAGGCAGGCAGCTGAGAGCTACTACCGCGCC TGGTGGCCGTGGCTCTGAAGAGGACGGGCCGGGCGAGGCAGGCAGCTGAGAGCTACTACCGCGCC A G SH3TC1 Ensembl:ENSG00000125089 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8228279..8228390 26863196 MeRIP-seq:(Medium) rs1169633206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19013627,Human_RBP_ID_27509576 RMVar_hsa_circ_80135,RMVar_hsa_circ_104979,RMVar_hsa_circ_224785,RMVar_hsa_circ_88219,RMVar_hsa_circ_105322,RMVar_hsa_circ_224786,RMVar_hsa_circ_224787,RMVar_hsa_circ_224789,RMVar_hsa_circ_77571,RMVar_hsa_circ_224790 76985 RMVar_ID_76985 Human_SNP_ID_172527655 m1A Human chr4 - 8229549 8229549 8229549 CAACTCTGCACCTCCCTGCATAGGCCCTGCTCACTCACCCCCACTTACACCCCACTCATCCCCGC CAACTCTGCACCTCCCTGCATAGGCCCTGCTCGCTCACCCCCACTTACACCCCACTCATCCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8229502..8229582 26863196 MeRIP-seq:(Medium) rs1240907974 Functional Loss SNV dbSNP153 33..33 33 - - - 76986 RMVar_ID_76986 Human_SNP_ID_172527658 m1A Human chr4 - 8229562 8229562 8229562 ACCAACCCACGCCCAACTCTGCACCTCCCTGCATAGGCCCTGCTCACTCACCCCCACTTACACCC ACCAACCCACGCCCAACTCTGCACCTCCCTGCGTAGGCCCTGCTCACTCACCCCCACTTACACCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8229512..8229873 26863196 MeRIP-seq:(Medium) rs1250422419 Functional Loss SNV dbSNP153 33..33 33 - - - 76987 RMVar_ID_76987 Human_SNP_ID_172541050 m1A Human chr4 + 8269816 8269816 8269816 CCCTGCGCCCTGGGGATGCCCCTGCCGCCCTGACGCCCGCCAGCCTGAGCCACCGGCGCATGTGA CCCTGCGCCCTGGGGATGCCCCTGCCGCCCTGCCGCCCGCCAGCCTGAGCCACCGGCGCATGTGA A C HTRA3 Ensembl:ENSG00000170801 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8269751..8270104 26863196 MeRIP-seq:(Medium) rs943225948 Functional Loss SNV dbSNP153 33..33 33 - - - 76988 RMVar_ID_76988 Human_SNP_ID_172552124 m1A Human chr4 - 8306461 8306459 8306461 AGGAGCAGGGGATACTGCAGATGGGTGTTCACAGGGGCAGAGGCGGGAAGCTAGGAGAGGAGGGG AGGAGCAGGGGATACTGCAGATGGGTGTTCAC__GGGCAGAGGCGGGAAGCTAGGAGAGGAGGGG CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8306411..8306586 26863196 MeRIP-seq:(Medium) rs1314848898 Functional Loss DEL dbSNP153 33..34 33 - - - 76989 RMVar_ID_76989 Human_SNP_ID_172552228 m1A Human chr4 - 8306817 8306817 8306817 CTGCAGGCTGCCCCATGGCCGCCTTGGGGAGGAGAAGCTTCCCCAGGCAGCAGCCAACTTTCCAC CTGCAGGCTGCCCCATGGCCGCCTTGGGGAGGCGAAGCTTCCCCAGGCAGCAGCCAACTTTCCAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8306767..8306951 26863196 MeRIP-seq:(Medium) rs1180419733 Functional Loss SNV dbSNP153 33..33 33 - - - 76990 RMVar_ID_76990 Human_SNP_ID_172571595 m1A Human chr4 - 8373382 8373382 8373382 CTACACGCACCCCCTTACCCAGACCGACACGCACCCCCTTAGCATCACCCAGAGCTGACACACAC CTACACGCACCCCCTTACCCAGACCGACACGCGCCCCCTTAGCATCACCCAGAGCTGACACACAC T C ACOX3 Ensembl:ENSG00000087008 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:8373334..8373493 26863196 MeRIP-seq:(Medium) rs539411373 Functional Loss SNV dbSNP153 33..33 33 - - - 76991 RMVar_ID_76991 Human_SNP_ID_172575396 m1A Human chr4 + 8385278 8385278 8385278 TGCCCACCTCACATGACCTCACCATGCACTCCACGTGACCTCACCGCTCCCCCACGTGACTCCAC TGCCCACCTCACATGACCTCACCATGCACTCCTCGTGACCTCACCGCTCCCCCACGTGACTCCAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8385229..8385391 26863196 MeRIP-seq:(Medium) rs904304322 Functional Loss SNV dbSNP153 33..33 33 - - - 76992 RMVar_ID_76992 Human_SNP_ID_172583680 m1A Human chr4 + 8412264 8412264 8412264 CCACTCTGAGAAGGAGCCTTGGCCCCACTCCCAAGGCCCCACAGCAGGGGCACCCTGTGCGAGGA CCACTCTGAGAAGGAGCCTTGGCCCCACTCCCCAGGCCCCACAGCAGGGGCACCCTGTGCGAGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8412253..8412369 32194978 MeRIP-seq:(Medium) rs935821925 Functional Loss SNV dbSNP153 33..33 33 - - - 76993 RMVar_ID_76993 Human_SNP_ID_172588347 m1A Human chr4 + 8428390 8428390 8428390 GCGCTCAGGGGATGCCTGTCGGCCCGCGACCGACTCGGAGTACTGGGACTAGCTGCCCGCACAGC GCGCTCAGGGGATGCCTGTCGGCCCGCGACCGCCTCGGAGTACTGGGACTAGCTGCCCGCACAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8428352..8428426 26863196 MeRIP-seq:(Medium) rs759998471 Functional Loss SNV dbSNP153 33..33 33 - - - 76994 RMVar_ID_76994 Human_SNP_ID_172588348 m1A Human chr4 + 8428390 8428390 8428390 GCGCTCAGGGGATGCCTGTCGGCCCGCGACCGACTCGGAGTACTGGGACTAGCTGCCCGCACAGC GCGCTCAGGGGATGCCTGTCGGCCCGCGACCGGCTCGGAGTACTGGGACTAGCTGCCCGCACAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8428352..8428426 26863196 MeRIP-seq:(Medium) rs759998471 Functional Loss SNV dbSNP153 33..33 33 - - - 76995 RMVar_ID_76995 Human_SNP_ID_172588364 m1A Human chr4 - 8428411 8428410 8428411 GGCCAGGCCAGAGACAGCTGCGCTGTGCGGGCAGCTAGTCCCAGTACTCCGAGTCGGTCGCGGGC GGCCAGGCCAGAGACAGCTGCGCTGTGCGGGC_GCTAGTCCCAGTACTCCGAGTCGGTCGCGGGC CT C ACOX3 Ensembl:ENSG00000087008 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8428254..8428426 26863196 MeRIP-seq:(Medium) rs1396534093 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4794871 Human_Splice_Rec_545199,Human_Splice_Rec_545267 76996 RMVar_ID_76996 Human_SNP_ID_172591713 m1A Human chr4 + 8440925 8440922 8440926 TCGAAGTGTGGCTGGAGAGGCCGCAGGTGGCAAACAAACGGCTTTGCGGCGCCCGCCTGGAGGCC TCGAAGTGTGGCTGGAGAGGCCGCAGGTGG____CAAACGGCTTTGCGGCGCCCGCCTGGAGGCC GCAAA G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8440881..8440965 26863196 MeRIP-seq:(Medium) rs1397114788 Functional Loss DEL dbSNP153 31..34 33 - - - 76997 RMVar_ID_76997 Human_SNP_ID_172591715 m1A Human chr4 + 8440925 8440925 8440925 TCGAAGTGTGGCTGGAGAGGCCGCAGGTGGCAAACAAACGGCTTTGCGGCGCCCGCCTGGAGGCC TCGAAGTGTGGCTGGAGAGGCCGCAGGTGGCAGACAAACGGCTTTGCGGCGCCCGCCTGGAGGCC A G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8440881..8440965 26863196 MeRIP-seq:(Medium) rs1011657696 Functional Loss SNV dbSNP153 33..33 33 - - - 76998 RMVar_ID_76998 Human_SNP_ID_172596868 m1A Human chr4 + 8459845 8459845 8459845 TTTATGGTCATGGGAAGGGGTGGGAGGCAGACACACAGCCAGTGTGTGCAGCAGGTTCGAGGGTG TTTATGGTCATGGGAAGGGGTGGGAGGCAGACGCACAGCCAGTGTGTGCAGCAGGTTCGAGGGTG A G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8459832..8459928 26863196 MeRIP-seq:(Medium) rs977315712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7235,RMVar_hsa_circ_64709 76999 RMVar_ID_76999 Human_SNP_ID_172600903 m1A Human chr4 + 8472285 8472285 8472285 AGGAGTCAGGAACAGAGAACAGCTTTAGGCAGAGCGAACAGCATTTGCAAAGAGCCAGGGTTGGG AGGAGTCAGGAACAGAGAACAGCTTTAGGCAGGGCGAACAGCATTTGCAAAGAGCCAGGGTTGGG A G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8472278..8472370 26863196 MeRIP-seq:(Medium) rs1422639227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15215002 77000 RMVar_ID_77000 Human_SNP_ID_172605111 m1A Human chr4 + 8485091 8485087 8485092 GAATAAGGTGAGAAGCAGAGGGGTGGAAATAAAGTAAATCATGAGAAAGAGCTTGGCTGAAGTAA GAATAAGGTGAGAAGCAGAGGGGTGGAAA_____TAAATCATGAGAAAGAGCTTGGCTGAAGTAA ATAAAG A TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8485042..8485215 26863196 MeRIP-seq:(Medium) rs1162736590 Functional Loss DEL dbSNP153 30..34 33 - - - 77001 RMVar_ID_77001 Human_SNP_ID_172605114 m1A Human chr4 + 8485104 8485104 8485104 AGCAGAGGGGTGGAAATAAAGTAAATCATGAGAAAGAGCTTGGCTGAAGTAATGAGGGCTGTCCC AGCAGAGGGGTGGAAATAAAGTAAATCATGAGCAAGAGCTTGGCTGAAGTAATGAGGGCTGTCCC A C TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:8485084..8485181 26863196 MeRIP-seq:(Medium) rs1441904896 Functional Loss SNV dbSNP153 33..33 33 - - - 77002 RMVar_ID_77002 Human_SNP_ID_172605115 m1A Human chr4 + 8485104 8485104 8485104 AGCAGAGGGGTGGAAATAAAGTAAATCATGAGAAAGAGCTTGGCTGAAGTAATGAGGGCTGTCCC AGCAGAGGGGTGGAAATAAAGTAAATCATGAGGAAGAGCTTGGCTGAAGTAATGAGGGCTGTCCC A G TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:8485084..8485181 26863196 MeRIP-seq:(Medium) rs1441904896 Functional Loss SNV dbSNP153 33..33 33 - - - 77003 RMVar_ID_77003 Human_SNP_ID_172605317 m1A Human chr4 + 8485775 8485775 8485775 CTCGGCCTAATAAGGGAACGGGGCAGGTGAGGATAACTAAAAAAGAGTGTATAAAAGAGTGTTGT CTCGGCCTAATAAGGGAACGGGGCAGGTGAGGGTAACTAAAAAAGAGTGTATAAAAGAGTGTTGT A G TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8485714..8485864 26863196 MeRIP-seq:(Medium) rs963822926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7333759 77004 RMVar_ID_77004 Human_SNP_ID_172605671 m1A Human chr4 + 8486898 8486884 8486899 GAAGAATTGGGACCTAGCTCAGCCCGGCGAGGAGCAGCCCAGGGAGGAGGGGAGAGGTCAGATGG GAAGAATTGGGACCTAGCT_______________CAGCCCAGGGAGGAGGGGAGAGGTCAGATGG TCAGCCCGGCGAGGAG T TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:8486847..8486930;chr4:8486783..8486945 26863196 MeRIP-seq:(Medium) rs1300470105 Functional Loss DEL dbSNP153 20..34 33 - - - 77005 RMVar_ID_77005 Human_SNP_ID_172605678 m1A Human chr4 + 8486901 8486893 8486901 GAATTGGGACCTAGCTCAGCCCGGCGAGGAGCAGCCCAGGGAGGAGGGGAGAGGTCAGATGGGTC GAATTGGGACCTAGCTCAGCCCGGC________GCCCAGGGAGGAGGGGAGAGGTCAGATGGGTC CGAGGAGCA C TRMT44,AC105345.1 Ensembl:ENSG00000155275,Ensembl:ENSG00000205959 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:8486853..8486926;chr4:8486783..8486940 26863196 MeRIP-seq:(Medium) rs1046227086 Functional Loss DEL dbSNP153 26..33 33 - - - 77006 RMVar_ID_77006 Human_SNP_ID_172612548 m1A Human chr4 - 8510285 8510285 8510285 CGGCTCTGAGATGGAGGAAGGTTCCCTAGCCCAGGAACGCGAGAGGCTTCCAGGAGCTGGAAAAG CGGCTCTGAGATGGAGGAAGGTTCCCTAGCCCTGGAACGCGAGAGGCTTCCAGGAGCTGGAAAAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8510204..8510311 32194978 MeRIP-seq:(Medium) rs752483249 Functional Loss SNV dbSNP153 33..33 33 - - - 77007 RMVar_ID_77007 Human_SNP_ID_172612549 m1A Human chr4 - 8510285 8510285 8510285 CGGCTCTGAGATGGAGGAAGGTTCCCTAGCCCAGGAACGCGAGAGGCTTCCAGGAGCTGGAAAAG CGGCTCTGAGATGGAGGAAGGTTCCCTAGCCCGGGAACGCGAGAGGCTTCCAGGAGCTGGAAAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8510204..8510311 32194978 MeRIP-seq:(Medium) rs752483249 Functional Loss SNV dbSNP153 33..33 33 - - - 77008 RMVar_ID_77008 Human_SNP_ID_172637459 m1A Human chr4 - 8592835 8592822 8592835 CTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTGGACGGCCAGCGC CTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGC_____________GGACCTTGGACGGCCAGCGC CGCCGCCCCACCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:8592785..8592956;chr4:8592791..8592918 26863196 MeRIP-seq:(Medium) rs1236250701 Functional Loss DEL dbSNP153 33..45 33 - - - 77009 RMVar_ID_77009 Human_SNP_ID_172637459 m1A Human chr4 + 8592834 8592822 8592835 TGCGCTGGCCGTCCAAGGTCCGCCGCCCCACCATGCCGCCCCCGCTGCCGCTGCTGCTCCTTACA TGCGCTGGCCGTCCAAGGTCC_____________GCCGCCCCCGCTGCCGCTGCTGCTCCTTACA CGCCGCCCCACCAT C GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8592783..8592910 26863196 MeRIP-seq:(Medium) rs1236250701 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_9334969 Human_Splice_Rec_545413,Human_Splice_Rec_545433,Human_Splice_Rec_545439,Human_Splice_Rec_545459,Human_Splice_Rec_545477,Human_Splice_Rec_545497,Human_Splice_Rec_545499,Human_Splice_Rec_545503 77010 RMVar_ID_77010 Human_SNP_ID_172637478 m1A Human chr4 + 8592834 8592834 8592834 TGCGCTGGCCGTCCAAGGTCCGCCGCCCCACCATGCCGCCCCCGCTGCCGCTGCTGCTCCTTACA TGCGCTGGCCGTCCAAGGTCCGCCGCCCCACCGTGCCGCCCCCGCTGCCGCTGCTGCTCCTTACA A G GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8592783..8592910 26863196 MeRIP-seq:(Medium) rs1379878882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334969 Human_Splice_Rec_545413,Human_Splice_Rec_545433,Human_Splice_Rec_545439,Human_Splice_Rec_545459,Human_Splice_Rec_545477,Human_Splice_Rec_545497,Human_Splice_Rec_545499,Human_Splice_Rec_545503 77011 RMVar_ID_77011 Human_SNP_ID_172637479 m1A Human chr4 - 8592835 8592835 8592835 CTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTGGACGGCCAGCGC CTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCTTGGTGGGGCGGCGGACCTTGGACGGCCAGCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:8592785..8592956;chr4:8592791..8592918 26863196 MeRIP-seq:(Medium) rs769050834 Functional Loss SNV dbSNP153 33..33 33 - - - 77012 RMVar_ID_77012 Human_SNP_ID_172637498 m1A Human chr4 - 8592847 8592844 8592847 CGACGACCAGGACTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG CGACGACCAGGACTGTAAGGAGCAGCAGCGGC___GGGGGCGGCATGGTGGGGCGGCGGACCTTG CGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8592800..8592910 26863196 MeRIP-seq:(Medium) rs768290580 Functional Loss DEL dbSNP153 33..35 33 - - - 77013 RMVar_ID_77013 Human_SNP_ID_172637509 m1A Human chr4 - 8592847 8592847 8592847 CGACGACCAGGACTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG CGACGACCAGGACTGTAAGGAGCAGCAGCGGCTGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8592800..8592910 26863196 MeRIP-seq:(Medium) rs2302583 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 77014 RMVar_ID_77014 Human_SNP_ID_172637510 m1A Human chr4 - 8592847 8592847 8592847 CGACGACCAGGACTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG CGACGACCAGGACTGTAAGGAGCAGCAGCGGCGGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8592800..8592910 26863196 MeRIP-seq:(Medium) rs2302583 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 77015 RMVar_ID_77015 Human_SNP_ID_172643019 m1A Human chr4 + 8606062 8606062 8606062 GAGGTGGCGGGCCGGGAGATGCTCATCTACCTAGCCCAGTACCTGTGCTCTGAGTACCTGCTTGG GAGGTGGCGGGCCGGGAGATGCTCATCTACCTCGCCCAGTACCTGTGCTCTGAGTACCTGCTTGG A C GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8587746..8606069 32194978 MeRIP-seq:(Medium) rs749078069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22770389 Human_Splice_Rec_545372,Human_Splice_Rec_545398,Human_Splice_Rec_545420,Human_Splice_Rec_545446,Human_Splice_Rec_545464,Human_Splice_Rec_545484 77016 RMVar_ID_77016 Human_SNP_ID_172643085 m1A Human chr4 - 8606151 8606151 8606151 CGGCAGCTGCCACCTCATAGCCGTCAGGGTTCATGGAGGGCAGCAGGTGGATGCGGGTGGTGTTG CGGCAGCTGCCACCTCATAGCCGTCAGGGTTCCTGGAGGGCAGCAGGTGGATGCGGGTGGTGTTG T G lnc-ACOX3-7 RNACentral:URS0000D5BD17 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8606101..8614384 32194978 MeRIP-seq:(Medium) rs780101270 Functional Loss SNV dbSNP153 33..33 33 - - - 77017 RMVar_ID_77017 Human_SNP_ID_172643210 m1A Human chr4 - 8606400 8606400 8606400 CACCATCGACTCCCTTTCCATCATTTTCCTCTATCACACGCATCACCTTTTTAATTCACCTAGAA CACCATCGACTCCCTTTCCATCATTTTCCTCTGTCACACGCATCACCTTTTTAATTCACCTAGAA T C lnc-ACOX3-7 RNACentral:URS0000D5BD17 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8606395..8606542 26863196 MeRIP-seq:(Medium) rs912949086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17525317,Human_RBP_ID_18030803 77018 RMVar_ID_77018 Human_SNP_ID_172645266 m1A Human chr4 - 8609192 8609192 8609192 AGTAAGTGAATGAGTAAGTGAGTGAGGGAGTGAGTGAATGCCTGAGTGAATGGGTGAGTGAATGA AGTAAGTGAATGAGTAAGTGAGTGAGGGAGTGGGTGAATGCCTGAGTGAATGGGTGAGTGAATGA T C lnc-ACOX3-7 RNACentral:URS0000D5BD17 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8609023..8609225 26863196 MeRIP-seq:(Medium) rs1160847009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24067922 77019 RMVar_ID_77019 Human_SNP_ID_172651236 m1A Human chr4 - 8619314 8619314 8619314 TTGATGACTTTGGCGTAGCCAGGGGCTTGGGCAATGACAATGTGGATACCTGGGGGCAGCAGTCT TTGATGACTTTGGCGTAGCCAGGGGCTTGGGCGATGACAATGTGGATACCTGGGGGCAGCAGTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:8619262..8619363 32194978 MeRIP-seq:(Medium) rs924282588 Functional Loss SNV dbSNP153 33..33 33 - - - 77020 RMVar_ID_77020 Human_SNP_ID_172651237 m1A Human chr4 - 8619314 8619314 8619314 TTGATGACTTTGGCGTAGCCAGGGGCTTGGGCAATGACAATGTGGATACCTGGGGGCAGCAGTCT TTGATGACTTTGGCGTAGCCAGGGGCTTGGGCCATGACAATGTGGATACCTGGGGGCAGCAGTCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:8619262..8619363 32194978 MeRIP-seq:(Medium) rs924282588 Functional Loss SNV dbSNP153 33..33 33 - - - 77021 RMVar_ID_77021 Human_SNP_ID_172651457 m1A Human chr4 + 8619529 8619529 8619529 CACGGAGCCCGACCCGCTCCGGGCGCGCAGGCAGCCCTCGGCCGACGGGAGTAAGCCCTGGTGGT CACGGAGCCCGACCCGCTCCGGGCGCGCAGGCGGCCCTCGGCCGACGGGAGTAAGCCCTGGTGGT A G GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:8619498..8619642 26863196 MeRIP-seq:(Medium) rs951794891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22770394 77022 RMVar_ID_77022 Human_SNP_ID_172651491 m1A Human chr4 - 8619564 8619564 8619564 TGGCCTGTGGGTGCTCAGCGATGTGAAGTAGGACCACCACCAGGGCTTACTCCCGTCGGCCGAGG TGGCCTGTGGGTGCTCAGCGATGTGAAGTAGGCCCACCACCAGGGCTTACTCCCGTCGGCCGAGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8619408..8619711 32194978 MeRIP-seq:(Medium) rs770727167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15217507 77023 RMVar_ID_77023 Human_SNP_ID_172651501 m1A Human chr4 + 8619575 8619575 8619575 GGGAGTAAGCCCTGGTGGTGGTCCTACTTCACATCGCTGAGCACCCACAGGCCACGCTGGCTGCT GGGAGTAAGCCCTGGTGGTGGTCCTACTTCACCTCGCTGAGCACCCACAGGCCACGCTGGCTGCT A C GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8619524..8619617 26863196 MeRIP-seq:(Medium) rs775559130 Functional Loss SNV dbSNP153 33..33 33 - - - 77024 RMVar_ID_77024 Human_SNP_ID_172651502 m1A Human chr4 + 8619575 8619575 8619575 GGGAGTAAGCCCTGGTGGTGGTCCTACTTCACATCGCTGAGCACCCACAGGCCACGCTGGCTGCT GGGAGTAAGCCCTGGTGGTGGTCCTACTTCACGTCGCTGAGCACCCACAGGCCACGCTGGCTGCT A G GPR78,CPZ Ensembl:ENSG00000155269,Ensembl:ENSG00000109625 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8619524..8619617 26863196 MeRIP-seq:(Medium) rs775559130 Functional Loss SNV dbSNP153 33..33 33 - - - 77025 RMVar_ID_77025 Human_SNP_ID_172721049 m1A Human chr4 + 8867835 8867832 8867835 GCGCGGGCGCGGCGGGCGCCAGCGGGAAGGGCAGGGTGGCCGGGGGCCCAGCGGCGGCTGCGGCC GCGCGGGCGCGGCGGGCGCCAGCGGGAAGG___GGGTGGCCGGGGGCCCAGCGGCGGCTGCGGCC GGCA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:8867745..8867895 26863410 MeRIP-seq:(Medium) rs1303930854 Functional Loss DEL dbSNP153 31..33 33 - - - 77026 RMVar_ID_77026 Human_SNP_ID_172722436 m1A Human chr4 + 8871749 8871728 8871749 ACCCGGACCGCTGGCGTCGGGCCCCGCAGGGCAGGCGGCGGCCTCCGCGCCGGGCTGGGCTGGGC ACCCGGACCGCT_____________________GGCGGCGGCCTCCGCGCCGGGCTGGGCTGGGC TGGCGTCGGGCCCCGCAGGGCA T - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr4:8871666..8871767 26863410 MeRIP-seq:(Medium) rs1231398536 Functional Loss DEL dbSNP153 13..33 33 - - - 77027 RMVar_ID_77027 Human_SNP_ID_173126695 m1A Human chr4 - 10075034 10075030 10075034 ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTATCTGTCAGGGGAGGTTGTACAGGTGAATGAGC ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACT____GTCAGGGGAGGTTGTACAGGTGAATGAGC CAGAT C WDR1 Ensembl:ENSG00000071127 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1289115138 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_24384755,Human_RBP_ID_26512251 Human_miRNA_ID_1268130 RMVar_hsa_circ_94689,RMVar_hsa_circ_117277,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224832,RMVar_hsa_circ_224829 77028 RMVar_ID_77028 Human_SNP_ID_173126699 m1A Human chr4 - 10075034 10075034 10075034 ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTATCTGTCAGGGGAGGTTGTACAGGTGAATGAGC ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTGTCTGTCAGGGGAGGTTGTACAGGTGAATGAGC T C WDR1 Ensembl:ENSG00000071127 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24384755,Human_RBP_ID_26512251 Human_miRNA_ID_1268130 GWAS_ID_9234,GWAS_ID_9235,GWAS_ID_9236,GWAS_ID_9237,GWAS_ID_9238,GWAS_ID_9239,GWAS_ID_9240,GWAS_ID_9241,GWAS_ID_9242,GWAS_ID_9243,GWAS_ID_9244 RMVar_hsa_circ_94689,RMVar_hsa_circ_117277,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224832,RMVar_hsa_circ_224829 77029 RMVar_ID_77029 Human_SNP_ID_173126701 m1A Human chr4 - 10075037 10075037 10075037 CACACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTATCTGTCAGGGGAGGTTGTACAGGTGAATG CACACAGAGCCCCTGGCCCCGCCGCGGCTCTCGCTATCTGTCAGGGGAGGTTGTACAGGTGAATG T C WDR1 Ensembl:ENSG00000071127 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:10074994..10075134 26863196 MeRIP-seq:(Medium) rs748741559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609934,Human_RBP_ID_4768177,Human_RBP_ID_24384755,Human_RBP_ID_26512251 Human_miRNA_ID_1268130 RMVar_hsa_circ_94689,RMVar_hsa_circ_117277,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224832,RMVar_hsa_circ_224829 77030 RMVar_ID_77030 Human_SNP_ID_173126753 m1A Human chr4 - 10075176 10075176 10075176 TTCTGAAAGCTTTAGACAGTAACAGTTTGCACATGAAAAATAAAGCGAGCACCTAAACAATGTGT TTCTGAAAGCTTTAGACAGTAACAGTTTGCACGTGAAAAATAAAGCGAGCACCTAAACAATGTGT T C WDR1 Ensembl:ENSG00000071127 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:10075126..10075250 32194978 MeRIP-seq:(Medium) rs932994873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609935,Human_RBP_ID_2808795,Human_RBP_ID_17521835,Human_RBP_ID_24027085,Human_RBP_ID_26825780 Human_miRNA_ID_1332804,Human_miRNA_ID_2180282,Human_miRNA_ID_2182390 RMVar_hsa_circ_94689,RMVar_hsa_circ_117277,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224832,RMVar_hsa_circ_224829 77031 RMVar_ID_77031 Human_SNP_ID_173130115 m1A Human chr4 + 10084465 10084465 10084465 CAAAGGATATTAATGTGTCCGTCGTGGCTCCCAGAGTAAATGTAGGACTTGCCGCCGTTTTTATG CAAAGGATATTAATGTGTCCGTCGTGGCTCCCCGAGTAAATGTAGGACTTGCCGCCGTTTTTATG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:10084451..10084475 26863196 MeRIP-seq:(Medium) rs768000682 Functional Loss SNV dbSNP153 33..33 33 - - - 77032 RMVar_ID_77032 Human_SNP_ID_173131371 m1A Human chr4 - 10087940 10087940 10087940 TGGCACATGACACACTGCTTTTTTCTGAATAGATTAGTTGGAGTCCCGACAGCACCCATTTGCTT TGGCACATGACACACTGCTTTTTTCTGAATAGGTTAGTTGGAGTCCCGACAGCACCCATTTGCTT T C WDR1 Ensembl:ENSG00000071127 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:10087926..10087950 32194978 MeRIP-seq:(Medium) rs763221944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22679749 Human_Splice_Rec_545816,Human_Splice_Rec_545836,Human_Splice_Rec_545862,Human_Splice_Rec_545902,Human_Splice_Rec_545920,Human_Splice_Rec_545938,Human_Splice_Rec_545946,Human_Splice_Rec_545954,Human_Splice_Rec_545960,Human_Splice_Rec_545966 RMVar_hsa_circ_8901,RMVar_hsa_circ_127946,RMVar_hsa_circ_122269,RMVar_hsa_circ_224829,RMVar_hsa_circ_16319,RMVar_hsa_circ_71998,RMVar_hsa_circ_224834,RMVar_hsa_circ_48704,RMVar_hsa_circ_113284,RMVar_hsa_circ_224838,RMVar_hsa_circ_336483,RMVar_hsa_circ_358797,RMVar_hsa_circ_377849,RMVar_hsa_circ_92567,RMVar_hsa_circ_224839,RMVar_hsa_circ_224840 77033 RMVar_ID_77033 Human_SNP_ID_173131748 m1A Human chr4 + 10088703 10088703 10088703 TCAGCACTGGCTGTGGCAAATCTGTTCCCATCAGGAGAGAATCGCACACAGTTGACAAAGCGGCT TCAGCACTGGCTGTGGCAAATCTGTTCCCATCGGGAGAGAATCGCACACAGTTGACAAAGCGGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:10088364..10091535 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 77034 RMVar_ID_77034 Human_SNP_ID_173134910 m1A Human chr4 + 10097888 10097888 10097888 GAAGAGCCACTATCCCAGAGGAAGACTGCTCCAAACCTTGACCCAATGACACAGGTGGAAGACAA GAAGAGCCACTATCCCAGAGGAAGACTGCTCCCAACCTTGACCCAATGACACAGGTGGAAGACAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:10097664..10097925 26863196 MeRIP-seq:(Medium) rs749023770 Functional Loss SNV dbSNP153 33..33 33 - - - 77035 RMVar_ID_77035 Human_SNP_ID_173137543 m1A Human chr4 - 10105038 10105038 10105038 GCACAGACTACACACAGACGTGGAGCTTAAACAGGATGGCAGAAGGTGGGCAGGAATCAGGGTCT GCACAGACTACACACAGACGTGGAGCTTAAACGGGATGGCAGAAGGTGGGCAGGAATCAGGGTCT T C WDR1 Ensembl:ENSG00000071127 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:10105034..10105107 26863196 MeRIP-seq:(Medium) rs1349709276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1207056 RMVar_hsa_circ_122269,RMVar_hsa_circ_224834,RMVar_hsa_circ_77371,RMVar_hsa_circ_92567,RMVar_hsa_circ_224840,RMVar_hsa_circ_80276,RMVar_hsa_circ_2023,RMVar_hsa_circ_224841,RMVar_hsa_circ_224842,RMVar_hsa_circ_112385,RMVar_hsa_circ_224847,RMVar_hsa_circ_83464,RMVar_hsa_circ_305919,RMVar_hsa_circ_224850 77036 RMVar_ID_77036 Human_SNP_ID_173139609 m1A Human chr4 + 10111230 10111230 10111230 AGGGCTGTGTGAGCCACCTGCCACCACTGCACACCAGCACTTCTCAGCCTGGGTCCTGTCCACTC AGGGCTGTGTGAGCCACCTGCCACCACTGCACCCCAGCACTTCTCAGCCTGGGTCCTGTCCACTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:10111228..10111334 26863196 MeRIP-seq:(Medium) rs1412863248 Functional Loss SNV dbSNP153 33..33 33 - - - 77037 RMVar_ID_77037 Human_SNP_ID_173141576 m1A Human chr4 - 10116236 10116236 10116236 CCTGACATGCCCCGCCGCATTTGTGTCTCCGCAGAGAAGGTGTTCGCCAGCCTCCCGCAGGTGGA CCTGACATGCCCCGCCGCATTTGTGTCTCCGCCGAGAAGGTGTTCGCCAGCCTCCCGCAGGTGGA T G WDR1 Ensembl:ENSG00000071127 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:10116101..10116278;chr4:10116201..10116250 26863196 MeRIP-seq:(Medium) rs112721334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_939934,Human_RBP_ID_22679052,Human_RBP_ID_22745788,Human_RBP_ID_26791126 RMVar_hsa_circ_122269,RMVar_hsa_circ_224834,RMVar_hsa_circ_77371,RMVar_hsa_circ_224841,RMVar_hsa_circ_112385,RMVar_hsa_circ_224847,RMVar_hsa_circ_83464,RMVar_hsa_circ_224850 77038 RMVar_ID_77038 Human_SNP_ID_173141805 m1A Human chr4 - 10116544 10116544 10116544 TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGAGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGGGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG T C WDR1 Ensembl:ENSG00000071127 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:10116542..10116800 26863196 MeRIP-seq:(Medium) rs908488610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_939606,Human_RBP_ID_5326356,Human_RBP_ID_5394002,Human_RBP_ID_9334641,Human_RBP_ID_19122297,Human_RBP_ID_22679053,Human_RBP_ID_26791217 RMVar_hsa_circ_122269,RMVar_hsa_circ_224834,RMVar_hsa_circ_77371,RMVar_hsa_circ_224841,RMVar_hsa_circ_112385,RMVar_hsa_circ_224847,RMVar_hsa_circ_83464,RMVar_hsa_circ_224850 77039 RMVar_ID_77039 Human_SNP_ID_173141806 m1A Human chr4 - 10116544 10116544 10116544 TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGAGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGCGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG T G WDR1 Ensembl:ENSG00000071127 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:10116542..10116800 26863196 MeRIP-seq:(Medium) rs908488610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_939606,Human_RBP_ID_5326356,Human_RBP_ID_5394002,Human_RBP_ID_9334641,Human_RBP_ID_19122297,Human_RBP_ID_22679053,Human_RBP_ID_26791217 RMVar_hsa_circ_122269,RMVar_hsa_circ_224834,RMVar_hsa_circ_77371,RMVar_hsa_circ_224841,RMVar_hsa_circ_112385,RMVar_hsa_circ_224847,RMVar_hsa_circ_83464,RMVar_hsa_circ_224850 77040 RMVar_ID_77040 Human_SNP_ID_173535178 m1A Human chr4 + 11372889 11372889 11372889 CACAGGAGCCGCTCCAGCTCCAACTCCTCCCAATAAACAGGCCACTGAAGCTCTCGCCCCTGTAA CACAGGAGCCGCTCCAGCTCCAACTCCTCCCAGTAAACAGGCCACTGAAGCTCTCGCCCCTGTAA A G RNPS1P1 Ensembl:ENSG00000250896 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:11372794..11372892 26863410 MeRIP-seq:(Medium) rs1319454463 Functional Loss SNV dbSNP153 33..33 33 - - - 77041 RMVar_ID_77041 Human_SNP_ID_174077565 m1A Human chr4 - 13247652 13247650 13247653 AAAGAAAAAGAAGAAACAGGAGGAGGAGAAGAAGGAAAAGAAGAAAGAAAGAAAAAGAAAGAAAG AAAGAAAAAGAAGAAACAGGAGGAGGAGAAG___GAAAAGAAGAAAGAAAGAAAAAGAAAGAAAG CCTT C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:13247578..13247707 26863196 MeRIP-seq:(Medium) rs900948518 Functional Loss DEL dbSNP153 32..34 33 - - - 77042 RMVar_ID_77042 Human_SNP_ID_174077575 m1A Human chr4 - 13247683 13247668 13247684 AAGAAAAAAGAAGAAAAAGAAGAAGAAGAAAAAAGAAAAAGAAGAAACAGGAGGAGGAGAAGAAG AAGAAAAAAGAAGAAAAAGAAGAAGAAGAAA________________CAGGAGGAGGAGAAGAAG GTTTCTTCTTTTTCTTT G lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:13247634..13247831 26863196 MeRIP-seq:(Medium) rs1285571113 Functional Loss DEL dbSNP153 32..47 33 - - - 77043 RMVar_ID_77043 Human_SNP_ID_174077602 m1A Human chr4 - 13247699 13247697 13247700 GAAGAAAAAGAAGAAGAAGAAAAAAGAAGAAAAAGAAGAAGAAGAAAAAAGAAAAAGAAGAAACA GAAGAAAAAGAAGAAGAAGAAAAAAGAAGAA___GAAGAAGAAGAAAAAAGAAAAAGAAGAAACA CTTT C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13247579..13247739 26863196 MeRIP-seq:(Medium) rs1386528083 Functional Loss DEL dbSNP153 32..34 33 - - - 77044 RMVar_ID_77044 Human_SNP_ID_174085914 m1A Human chr4 - 13280720 13280720 13280720 TGGAGAAAGAGAGGCAAAGATGGAAGCAAAAGAGGCAGCAAGGCAGGCGCTGACTGGTAACAACA TGGAGAAAGAGAGGCAAAGATGGAAGCAAAAGTGGCAGCAAGGCAGGCGCTGACTGGTAACAACA T A lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13280564..13280829 26863196 MeRIP-seq:(Medium) rs946123237 Functional Loss SNV dbSNP153 33..33 33 - - - 77045 RMVar_ID_77045 Human_SNP_ID_174086037 m1A Human chr4 - 13281164 13281162 13281164 GAACGATACAGAAACAAGATAAGGACACAGAGAGGAACAGAGGAAGGAGAGGGACAAGGAGAGAA GAACGATACAGAAACAAGATAAGGACACAGAG__GAACAGAGGAAGGAGAGGGACAAGGAGAGAA CCT C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13281115..13281245 26863196 MeRIP-seq:(Medium) rs1192984635 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15047721 77046 RMVar_ID_77046 Human_SNP_ID_174086039 m1A Human chr4 - 13281164 13281164 13281164 GAACGATACAGAAACAAGATAAGGACACAGAGAGGAACAGAGGAAGGAGAGGGACAAGGAGAGAA GAACGATACAGAAACAAGATAAGGACACAGAGGGGAACAGAGGAAGGAGAGGGACAAGGAGAGAA T C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13281115..13281245 26863196 MeRIP-seq:(Medium) rs1308736667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15047721 77047 RMVar_ID_77047 Human_SNP_ID_174137837 m1A Human chr4 + 13484192 13484179 13484192 GGAACCAGGCCCGCCCCTCGAGGTGGGGGGGGAAGGGAAGGATGAAGGCTCCGGGGGCGGGGGAG GGAACCAGGCCCGCCCCTCG_____________AGGGAAGGATGAAGGCTCCGGGGGCGGGGGAG GAGGTGGGGGGGGA G lnc-CPEB2-13 RNACentral:URS00008B8CAC lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:13484150..13484325 26863196 MeRIP-seq:(Medium) rs1350463578 Functional Loss DEL dbSNP153 21..33 33 - - - 77048 RMVar_ID_77048 Human_SNP_ID_174137859 m1A Human chr4 + 13484192 13484192 13484192 GGAACCAGGCCCGCCCCTCGAGGTGGGGGGGGAAGGGAAGGATGAAGGCTCCGGGGGCGGGGGAG GGAACCAGGCCCGCCCCTCGAGGTGGGGGGGGGAGGGAAGGATGAAGGCTCCGGGGGCGGGGGAG A G lnc-CPEB2-13 RNACentral:URS00008B8CAC lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:13484150..13484325 26863196 MeRIP-seq:(Medium) rs775406044 Functional Loss SNV dbSNP153 33..33 33 - - - 77049 RMVar_ID_77049 Human_SNP_ID_174137864 m1A Human chr4 - 13484202 13484202 13484202 CCTTCCTCCTCTCCCCCGCCCCCGGAGCCTTCATCCTTCCCTTCCCCCCCCACCTCGAGGGGCGG CCTTCCTCCTCTCCCCCGCCCCCGGAGCCTTCTTCCTTCCCTTCCCCCCCCACCTCGAGGGGCGG T A RAB28 Ensembl:ENSG00000157869 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:13484153..13484231 32194978 MeRIP-seq:(Medium) rs768478952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4773156,Human_RBP_ID_5448234 Human_miRNA_ID_2945118 RMVar_hsa_circ_224863,RMVar_hsa_circ_121593 77050 RMVar_ID_77050 Human_SNP_ID_174137865 m1A Human chr4 + 13484205 13484205 13484205 CCCCTCGAGGTGGGGGGGGAAGGGAAGGATGAAGGCTCCGGGGGCGGGGGAGAGGAGGAAGGGAG CCCCTCGAGGTGGGGGGGGAAGGGAAGGATGACGGCTCCGGGGGCGGGGGAGAGGAGGAAGGGAG A C lnc-CPEB2-13 RNACentral:URS00008B8CAC lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr4:13484101..13484325;chr4:13484154..13484298 26863196 MeRIP-seq:(Medium) rs1023146558 Functional Loss SNV dbSNP153 33..33 33 - - - 77051 RMVar_ID_77051 Human_SNP_ID_174154301 m1A Human chr4 - 13542402 13542400 13542403 CGGGCCGGCAGGCGTCGCGGAGGAGGAGGAGGAGCCGGCGGCGCCCAAGCCACGCAAGAAGCGCT CGGGCCGGCAGGCGTCGCGGAGGAGGAGGAG___CCGGCGGCGCCCAAGCCACGCAAGAAGCGCT GCTC G NKX3-2 Ensembl:ENSG00000109705 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:13542351..13544242;chr4:13542291..13542459 26863196 MeRIP-seq:(Medium) rs746991447 Functional Loss DEL dbSNP153 32..34 33 - - - 77052 RMVar_ID_77052 Human_SNP_ID_174154877 m1A Human chr4 + 13544138 13544138 13544138 GCTCTCGTTCTCCTCGCTGAGCGCGGAGTCCGAGTCCCAGCCTTCCGGGCTCTCCGCAGTCCGCC GCTCTCGTTCTCCTCGCTGAGCGCGGAGTCCGTGTCCCAGCCTTCCGGGCTCTCCGCAGTCCGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:13544035..13544264 26863196 MeRIP-seq:(Medium) rs751869344 Functional Loss SNV dbSNP153 33..33 33 - - - 77053 RMVar_ID_77053 Human_SNP_ID_174169522 m1A Human chr4 + 13601197 13601197 13601197 ACCACAGTACCAATCTGACTGTCCCCTTCTGCACTTTCACAAATCAAGACCCCTTCACTTTCTTC ACCACAGTACCAATCTGACTGTCCCCTTCTGCCCTTTCACAAATCAAGACCCCTTCACTTTCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:13601146..13601374 26863196 MeRIP-seq:(Medium) rs763935230 Functional Loss SNV dbSNP153 33..33 33 - - - 77054 RMVar_ID_77054 Human_SNP_ID_174169537 m1A Human chr4 + 13601278 13601278 13601278 GTTGAAGCATGCCCAATTTCATTTCCTCTTCCAGTACTAGTCACAACATCCTCCCCTTCCTCGTC GTTGAAGCATGCCCAATTTCATTTCCTCTTCCCGTACTAGTCACAACATCCTCCCCTTCCTCGTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:13601184..13601325 26863196 MeRIP-seq:(Medium) rs1384209886 Functional Loss SNV dbSNP153 33..33 33 - - - 77055 RMVar_ID_77055 Human_SNP_ID_174169610 m1A Human chr4 + 13601476 13601476 13601476 CTTATAGCAAAGCCTTCGCTGCTATCTTCTGAACCTGTGCAACTTGCTGGCCCCTCTCCATCTTC CTTATAGCAAAGCCTTCGCTGCTATCTTCTGATCCTGTGCAACTTGCTGGCCCCTCTCCATCTTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:13601426..13601794 26863196 MeRIP-seq:(Medium) rs751909184 Functional Loss SNV dbSNP153 33..33 33 - - - 77056 RMVar_ID_77056 Human_SNP_ID_174169638 m1A Human chr4 - 13601576 13601576 13601576 TAATGATGCACCACCAGGAACAAGTGCCAGCCAAGAAGGAGATGGTTCTGTGAATGATGGTACAG TAATGATGCACCACCAGGAACAAGTGCCAGCCTAGAAGGAGATGGTTCTGTGAATGATGGTACAG T A BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:13601527..13601634 32194978 MeRIP-seq:(Medium) rs61995954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91864,RMVar_hsa_circ_224876,RMVar_hsa_circ_101305,RMVar_hsa_circ_224880,RMVar_hsa_circ_265090 77057 RMVar_ID_77057 Human_SNP_ID_174169639 m1A Human chr4 - 13601576 13601576 13601576 TAATGATGCACCACCAGGAACAAGTGCCAGCCAAGAAGGAGATGGTTCTGTGAATGATGGTACAG TAATGATGCACCACCAGGAACAAGTGCCAGCCCAGAAGGAGATGGTTCTGTGAATGATGGTACAG T G BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:13601527..13601634 32194978 MeRIP-seq:(Medium) rs61995954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91864,RMVar_hsa_circ_224876,RMVar_hsa_circ_101305,RMVar_hsa_circ_224880,RMVar_hsa_circ_265090 77058 RMVar_ID_77058 Human_SNP_ID_174170399 m1A Human chr4 + 13603704 13603704 13603704 TCCTCTCCGATTTTCGCACAACCTTCTACTTAATTTCTTTTCCATGAGTGAACTATTACCTCTGG TCCTCTCCGATTTTCGCACAACCTTCTACTTAGTTTCTTTTCCATGAGTGAACTATTACCTCTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:13603653..13603742 26863196 MeRIP-seq:(Medium) rs1431274036 Functional Loss SNV dbSNP153 33..33 33 - - - 77059 RMVar_ID_77059 Human_SNP_ID_174170761 m1A Human chr4 - 13604791 13604791 13604791 CAGAAAAGCACACTTAAAAACGAAAAGCATCTAAAGAAAGATGATTCTGAAACACCACATTTGAA CAGAAAAGCACACTTAAAAACGAAAAGCATCTGAAGAAAGATGATTCTGAAACACCACATTTGAA T C BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:13604740..13604845 26863196 MeRIP-seq:(Medium) rs200983981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70608,Human_RBP_ID_2819819 RMVar_hsa_circ_91864,RMVar_hsa_circ_224876,RMVar_hsa_circ_101305,RMVar_hsa_circ_224880,RMVar_hsa_circ_265090 77060 RMVar_ID_77060 Human_SNP_ID_174176114 m1A Human chr4 - 13626690 13626690 13626690 GAGGTGACAGCAGATACTGAAGTGGAGAAAGGACAGGAAAGAGAGCAGATTCAGGAGAGTAATGT GAGGTGACAGCAGATACTGAAGTGGAGAAAGGCCAGGAAAGAGAGCAGATTCAGGAGAGTAATGT T G BOD1L1 Ensembl:ENSG00000038219 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13626538..13626850 26863196 MeRIP-seq:(Medium) rs962152192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15050787 77061 RMVar_ID_77061 Human_SNP_ID_174176350 m1A Human chr4 + 13627540 13627510 13627540 GGCGGTGGCTGCGGCTGCGGCTGCGGCGGGGGAGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG GGC______________________________GGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG CGGTGGCTGCGGCTGCGGCTGCGGCGGGGGA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:13627476..13627700 26863196 MeRIP-seq:(Medium) rs1414382515 Functional Loss DEL dbSNP153 4..33 33 - - - 77062 RMVar_ID_77062 Human_SNP_ID_174176369 m1A Human chr4 + 13627555 13627537 13627555 TGCGGCTGCGGCGGGGGAGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTGTGGGTTGGTGGCCAT TGCGGCTGCGGCGGG__________________GGAGGCGGCTGCGGCTGTGGGTTGGTGGCCAT GGGAGGCGGCGGCGCCGGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:13627449..13627683 26863196 MeRIP-seq:(Medium) rs1361088625 Functional Loss DEL dbSNP153 16..33 33 - - - 77063 RMVar_ID_77063 Human_SNP_ID_174176371 m1A Human chr4 + 13627540 13627540 13627540 GGCGGTGGCTGCGGCTGCGGCTGCGGCGGGGGAGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG GGCGGTGGCTGCGGCTGCGGCTGCGGCGGGGGGGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:13627476..13627700 26863196 MeRIP-seq:(Medium) rs945329219 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 77064 RMVar_ID_77064 Human_SNP_ID_174176380 m1A Human chr4 - 13627573 13627573 13627573 TCCCCGGCACAGGCCACCATGGCCACCAACCCACAGCCGCAGCCGCCTCCTCCGGCGCCGCCGCC TCCCCGGCACAGGCCACCATGGCCACCAACCCCCAGCCGCAGCCGCCTCCTCCGGCGCCGCCGCC T G BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13627525..13627663 26863196 MeRIP-seq:(Medium) rs185332136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249282,Human_RBP_ID_786859,Human_RBP_ID_9304141 77065 RMVar_ID_77065 Human_SNP_ID_174183137 m1A Human chr4 - 13654397 13654397 13654397 ATGTCAAGAAGCCTGCACAAAAATTATCACCAAGCCGGGGCTGCAAAGTCACAGAAGGACCAGTT ATGTCAAGAAGCCTGCACAAAAATTATCACCACGCCGGGGCTGCAAAGTCACAGAAGGACCAGTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:13654349..13654490 26863196 MeRIP-seq:(Medium) rs992127235 Functional Loss SNV dbSNP153 33..33 33 - - - 77066 RMVar_ID_77066 Human_SNP_ID_31906977 m1A Human chr1 - 143800067 143800067 143800067 CAGTGGTAGGGTTCTCGCCTCACACGCGGGAGACCCGGGTTCAATTCCCGGTCAAGGCAAGAGGT CAGTGGTAGGGTTCTCGCCTCACACGCGGGAGGCCCGGGTTCAATTCCCGGTCAAGGCAAGAGGT T C TRV-CAC8-1-001,tRNA-Val-CAC-8-1 RNACentral:URS0000676AD7,RNACentral:URS00006C00AA tRNA,tRNA intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:143800035..143800119 26863410 MeRIP-seq:(Medium) rs587649621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1232713,Human_RBP_ID_1250008,Human_RBP_ID_1344615,Human_RBP_ID_1410952,Human_RBP_ID_1724742,Human_RBP_ID_3280255,Human_RBP_ID_5092450,Human_RBP_ID_5254174,Human_RBP_ID_5685003,Human_RBP_ID_8053579,Human_RBP_ID_8240146,Human_RBP_ID_8284277,Human_RBP_ID_8734351,Human_RBP_ID_8955528,Human_RBP_ID_10564820,Human_RBP_ID_16969861,Human_RBP_ID_17072875,Human_RBP_ID_17667602,Human_RBP_ID_17674921,Human_RBP_ID_17724528,Human_RBP_ID_18428475,Human_RBP_ID_18508592,Human_RBP_ID_18524436,Human_RBP_ID_18550641,Human_RBP_ID_19151374,Human_RBP_ID_22779714,Human_RBP_ID_23121339,Human_RBP_ID_23263471,Human_RBP_ID_23330062,Human_RBP_ID_24447000,Human_RBP_ID_26367614,Human_RBP_ID_27167265,Human_RBP_ID_27578227 77067 RMVar_ID_77067 Human_SNP_ID_31993028 m1A Human chr1 + 144412601 144412601 144412601 AAAGCTCATACTTACTTGGCGGGGGAGATACCATGATCACGAAGGTGGTTTTCTCAGGGCGAGGC AAAGCTCATACTTACTTGGCGGGGGAGATACCGTGATCACGAAGGTGGTTTTCTCAGGGCGAGGC A G RNVU1-15 Ensembl:ENSG00000207205 snRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:144412576..144412600 26863196 MeRIP-seq:(Medium) rs1420684783 Functional Loss SNV dbSNP153 33..33 33 - - - 77068 RMVar_ID_77068 Human_SNP_ID_31993147 m1A Human chr1 + 144412685 144412685 144412685 TGTACTGACCCCTGCCATTTTCCCCCAATGTGAGGAACTCGACTGCATAACTTGTGATAGTAGGG TGTACTGACCCCTGCCATTTTCCCCCAATGTGGGGAACTCGACTGCATAACTTGTGATAGTAGGG A G RNVU1-15 Ensembl:ENSG00000207205 snRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:144412636..144412756;chr1:144412635..144412767 26863196 MeRIP-seq:(Medium) rs376488100 Functional Loss SNV dbSNP153 33..33 33 - - - 77069 RMVar_ID_77069 Human_SNP_ID_31996221 m1A Human chr1 + 144419325 144419325 144419325 ATTCGGCTGTTAACCGAAAGGTTGGTGGTTCGAGCCCACCCAGGGACGCTTGTTTGAGCTTTTAA ATTCGGCTGTTAACCGAAAGGTTGGTGGTTCGGGCCCACCCAGGGACGCTTGTTTGAGCTTTTAA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1553537775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26747053 77070 RMVar_ID_77070 Human_SNP_ID_31997658 m1A Human chr1 - 144422141 144422140 144422142 ATATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA ATATCACCACAAATCACACAACAAAAAGGAG__GAGATATTTTGGGTTCAAAAAAAGTAAAAAGA CTT C NBPF15 Ensembl:ENSG00000266338 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1170183866 Functional Loss DEL dbSNP153 32..33 33 - - - 77071 RMVar_ID_77071 Human_SNP_ID_31997662 m1A Human chr1 - 144422147 144422147 144422147 TAGTCCATATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTA TAGTCCATATCACCACAAATCACACAACAAAAGGGAGAAGAGATATTTTGGGTTCAAAAAAAGTA T C NBPF15 Ensembl:ENSG00000266338 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1186470956 Functional Loss SNV dbSNP153 33..33 33 - - - 77072 RMVar_ID_77072 Human_SNP_ID_32013838 m1A Human chr1 - 144461470 144461468 144461470 TGTGGCGCCAGGAGCGGGCCGAGGCGTGGCGCACGGATGCCGTCTGGATGGGAAGTTACGGTTTA TGTGGCGCCAGGAGCGGGCCGAGGCGTGGCGC__GGATGCCGTCTGGATGGGAAGTTACGGTTTA CGT C NBPF15 Ensembl:ENSG00000266338 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:144461426..144461592 26863196 MeRIP-seq:(Medium) rs1553548515 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_851696,Human_RBP_ID_3333081,Human_RBP_ID_5338286,Human_RBP_ID_10564271,Human_RBP_ID_22871629,Human_RBP_ID_27835276 Human_Splice_Rec_117121,Human_Splice_Rec_117159,Human_Splice_Rec_117199,Human_Splice_Rec_117209,Human_Splice_Rec_117215 77073 RMVar_ID_77073 Human_SNP_ID_32013842 m1A Human chr1 - 144461470 144461470 144461470 TGTGGCGCCAGGAGCGGGCCGAGGCGTGGCGCACGGATGCCGTCTGGATGGGAAGTTACGGTTTA TGTGGCGCCAGGAGCGGGCCGAGGCGTGGCGCGCGGATGCCGTCTGGATGGGAAGTTACGGTTTA T C NBPF15 Ensembl:ENSG00000266338 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:144461426..144461592 26863196 MeRIP-seq:(Medium) rs781899308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851696,Human_RBP_ID_3333081,Human_RBP_ID_5338286,Human_RBP_ID_10564271,Human_RBP_ID_22871629,Human_RBP_ID_27835276 Human_Splice_Rec_117121,Human_Splice_Rec_117159,Human_Splice_Rec_117199,Human_Splice_Rec_117209,Human_Splice_Rec_117215 77074 RMVar_ID_77074 Human_SNP_ID_32013848 m1A Human chr1 + 144461476 144461476 144461476 GTAACTTCCCATCCAGACGGCATCCGTGCGCCACGCCTCGGCCCGCTCCTGGCGCCACAGGTCGC GTAACTTCCCATCCAGACGGCATCCGTGCGCCGCGCCTCGGCCCGCTCCTGGCGCCACAGGTCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:144461376..144461651;chr1:144460907..144461650 26863196 MeRIP-seq:(Medium) rs587694535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224851,Human_RBP_ID_746820 77075 RMVar_ID_77075 Human_SNP_ID_32013925 m1A Human chr1 - 144461585 144461585 144461585 ATGGGCTGGGCGGCGGTTGAGACAGCGGCGGTATCGGGAGGGGTAGGTGAGGGTCGCGAGGCTGC ATGGGCTGGGCGGCGGTTGAGACAGCGGCGGTCTCGGGAGGGGTAGGTGAGGGTCGCGAGGCTGC T G NBPF15 Ensembl:ENSG00000266338 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:144460957..144461650 26863196 MeRIP-seq:(Medium) rs1437038194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3990726 77076 RMVar_ID_77076 Human_SNP_ID_32153274 m1A Human chr1 - 145096638 145096638 145096638 GTATTTATTGAGTAGGAACAGGGGAGCGTGGTAAACTTGGCTTTCCTTTTAACTTTTGGAGAAGG GTATTTATTGAGTAGGAACAGGGGAGCGTGGTGAACTTGGCTTTCCTTTTAACTTTTGGAGAAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:145096581..145096669;chr1:145096565..145096670 26863196 MeRIP-seq:(Medium) rs1370720932 Functional Loss SNV dbSNP153 33..33 33 - - - 77077 RMVar_ID_77077 Human_SNP_ID_32157203 m1A Human chr1 + 145129297 145129297 145129297 GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGAACCCACCCAGAGGCGTCGCTGATATTTTATAA GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGCACCCACCCAGAGGCGTCGCTGATATTTTATAA A C - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1352766809 Functional Loss SNV dbSNP153 33..33 33 - - - 77078 RMVar_ID_77078 Human_SNP_ID_32157204 m1A Human chr1 + 145129297 145129297 145129297 GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGAACCCACCCAGAGGCGTCGCTGATATTTTATAA GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGGACCCACCCAGAGGCGTCGCTGATATTTTATAA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1352766809 Functional Loss SNV dbSNP153 33..33 33 - - - 77079 RMVar_ID_77079 Human_SNP_ID_32157205 m1A Human chr1 + 145129297 145129297 145129297 GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGAACCCACCCAGAGGCGTCGCTGATATTTTATAA GTTTGGCTGTTAACTAAAAGGTTGGCGGTTCGTACCCACCCAGAGGCGTCGCTGATATTTTATAA A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1352766809 Functional Loss SNV dbSNP153 33..33 33 - - - 77080 RMVar_ID_77080 Human_SNP_ID_32174283 m1A Human chr1 - 145215295 145215295 145215295 AAGCACGCCTCCTGGGTTCCAGCAGCGGCGGCACAGCGGGGTTGGTTGGACCCGCCAGGTTTGCG AAGCACGCCTCCTGGGTTCCAGCAGCGGCGGCGCAGCGGGGTTGGTTGGACCCGCCAGGTTTGCG T C LINC01145 Ensembl:ENSG00000272419 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145215262..145215329 26863196 MeRIP-seq:(Medium) rs1413989494 Functional Loss SNV dbSNP153 33..33 33 - - - 77081 RMVar_ID_77081 Human_SNP_ID_32193514 m1A Human chr1 - 145281175 145281175 145281175 CAGGGGTCAGCACATCCGGAACGCAATGGATAAGCTTCGCCCTGAGAAAAACCACCTTCGTGATC CAGGGGTCAGCACATCCGGAACGCAATGGATACGCTTCGCCCTGAGAAAAACCACCTTCGTGATC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:145281151..145281175 26863196 MeRIP-seq:(Medium) rs116704620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23111130,Human_RBP_ID_26575606 77082 RMVar_ID_77082 Human_SNP_ID_32193523 m1A Human chr1 + 145281181 145281181 145281181 GAAGGTGGTTTTTCTCAGGGCGAAGCTTATCCATTGCGTTCCGGATGTGCTGACCCCTGCGATTT GAAGGTGGTTTTTCTCAGGGCGAAGCTTATCCCTTGCGTTCCGGATGTGCTGACCCCTGCGATTT A C AC245014.3,RNVU1-14 Ensembl:ENSG00000276216,Ensembl:ENSG00000207501 lincRNA,snRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145281126..145281285 26863196 MeRIP-seq:(Medium) rs1231452245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074325,Human_RBP_ID_5312657,Human_RBP_ID_19038956,Human_RBP_ID_24358468,Human_RBP_ID_26774486 77083 RMVar_ID_77083 Human_SNP_ID_32193524 m1A Human chr1 + 145281181 145281181 145281181 GAAGGTGGTTTTTCTCAGGGCGAAGCTTATCCATTGCGTTCCGGATGTGCTGACCCCTGCGATTT GAAGGTGGTTTTTCTCAGGGCGAAGCTTATCCGTTGCGTTCCGGATGTGCTGACCCCTGCGATTT A G AC245014.3,RNVU1-14 Ensembl:ENSG00000276216,Ensembl:ENSG00000207501 lincRNA,snRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145281126..145281285 26863196 MeRIP-seq:(Medium) rs1231452245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074325,Human_RBP_ID_5312657,Human_RBP_ID_19038956,Human_RBP_ID_24358468,Human_RBP_ID_26774486 77084 RMVar_ID_77084 Human_SNP_ID_32193568 m1A Human chr1 - 145281206 145281206 145281206 GCACTCGAGTTTCCCACACTTGGGGAAATCGCAGGGGTCAGCACATCCGGAACGCAATGGATAAG GCACTCGAGTTTCCCACACTTGGGGAAATCGCTGGGGTCAGCACATCCGGAACGCAATGGATAAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:145281155..145281235 26863196 MeRIP-seq:(Medium) rs587602828 Functional Loss SNV dbSNP153 33..33 33 - - - 77085 RMVar_ID_77085 Human_SNP_ID_32193569 m1A Human chr1 - 145281206 145281206 145281206 GCACTCGAGTTTCCCACACTTGGGGAAATCGCAGGGGTCAGCACATCCGGAACGCAATGGATAAG GCACTCGAGTTTCCCACACTTGGGGAAATCGCCGGGGTCAGCACATCCGGAACGCAATGGATAAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:145281155..145281235 26863196 MeRIP-seq:(Medium) rs587602828 Functional Loss SNV dbSNP153 33..33 33 - - - 77086 RMVar_ID_77086 Human_SNP_ID_32222824 m1A Human chr1 + 145459714 145459714 145459714 CTCTGGACTCTGAATCCAGCGATCCGAGTTCGAGTCTCGGTGGAACCTTTCTGTTTAATTAGGAC CTCTGGACTCTGAATCCAGCGATCCGAGTTCGGGTCTCGGTGGAACCTTTCTGTTTAATTAGGAC A G HSALNG0006639-001 RNACentral:URS0000EAD01C lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1300824139 Functional Loss SNV dbSNP153 33..33 33 - - - 77087 RMVar_ID_77087 Human_SNP_ID_32224320 m1A Human chr1 - 145465663 145465663 145465663 CCCCTGCGATTTCCCCAAATGTGGGAAACTTGACTGCATAATTTGTGGTAGTGGGGGACTGCGTT CCCCTGCGATTTCCCCAAATGTGGGAAACTTGGCTGCATAATTTGTGGTAGTGGGGGACTGCGTT T C RNVU1-31 Ensembl:ENSG00000270722 snRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:145465626..145465700 26863196 MeRIP-seq:(Medium) rs1338080971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17341697 77088 RMVar_ID_77088 Human_SNP_ID_32224439 m1A Human chr1 + 145465739 145465739 145465739 GGAGTGCAATGGATAAGCCTCGCCCAGGGAAAACCACCTTCGTGATCATGGTATCTCCCCTGCCA GGAGTGCAATGGATAAGCCTCGCCCAGGGAAACCCACCTTCGTGATCATGGTATCTCCCCTGCCA A C HSALNG0006752-001 RNACentral:URS0000EAFD7B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:145465626..145465775;chr1:145465726..145465750;chr1:145465639..145465775 26863196 MeRIP-seq:(Medium) rs1383638896 Functional Loss SNV dbSNP153 33..33 33 - - - 77089 RMVar_ID_77089 Human_SNP_ID_32283027 m1A Human chr1 - 145733708 145733708 145733708 GACAAAAGAACAGCCAGGTGGGTAGAACAGCCAGGGGAGTACAGTCACAGAAGCCACTGGAGATG GACAAAAGAACAGCCAGGTGGGTAGAACAGCCGGGGGAGTACAGTCACAGAAGCCACTGGAGATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145733588..145733914 26863196 MeRIP-seq:(Medium) rs1242223691 Functional Loss SNV dbSNP153 33..33 33 - - - 77090 RMVar_ID_77090 Human_SNP_ID_32283068 m1A Human chr1 - 145733870 145733870 145733870 AAGCTGGAGAAGTTGATTTGCTGGTCAGTTGCAGGGAGATGCTGGTTTAAATCGTGGGTAGATGA AAGCTGGAGAAGTTGATTTGCTGGTCAGTTGCGGGGAGATGCTGGTTTAAATCGTGGGTAGATGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145733603..145733910 26863196 MeRIP-seq:(Medium) rs1559094837 Functional Loss SNV dbSNP153 33..33 33 - - - 77091 RMVar_ID_77091 Human_SNP_ID_32285858 m1A Human chr1 - 145745370 145745370 145745370 ACGATCTCAGCTCACCACAGCCTCGACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTACCA ACGATCTCAGCTCACCACAGCCTCGACCTCCCGGGCTCAAGTGATCCTCCCACCTCAGCCTACCA T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1378794966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10560630,Human_RBP_ID_18550332 77092 RMVar_ID_77092 Human_SNP_ID_32285982 m1A Human chr1 - 145745816 145745816 145745816 TCCCATTCCTTTTTGGGAATGAGTTGGGCAGCATACAGGCACAGAAAGACAGATGTTTGAGACCT TCCCATTCCTTTTTGGGAATGAGTTGGGCAGCGTACAGGCACAGAAAGACAGATGTTTGAGACCT T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17354678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10560616,Human_RBP_ID_18550331 GWAS_ID_9245,GWAS_ID_9246,GWAS_ID_9247,GWAS_ID_9248,GWAS_ID_9249 77093 RMVar_ID_77093 Human_SNP_ID_32306632 m1A Human chr1 + 145823899 145823899 145823899 CCGCCATTTTTGCCCTCCGCCGCGGCCGTCCGAGAGGGCAGCCGGCCCGTCCCTCGCCAGGCCGC CCGCCATTTTTGCCCTCCGCCGCGGCCGTCCGGGAGGGCAGCCGGCCCGTCCCTCGCCAGGCCGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:145823850..145824028 26863196 MeRIP-seq:(Medium) rs896586281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_857282 77094 RMVar_ID_77094 Human_SNP_ID_32306644 m1A Human chr1 - 145823916 145823915 145823916 CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGGACGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGG_CGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG GT G RNF115 Ensembl:ENSG00000265491 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:145823851..145824033;chr1:145823751..145824327;chr1:145823751..145824187 26863196 MeRIP-seq:(Medium) rs1553725020 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4072995,Human_RBP_ID_18968765,Human_RBP_ID_22871830 77095 RMVar_ID_77095 Human_SNP_ID_32306645 m1A Human chr1 - 145823916 145823916 145823916 CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGGACGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGGGCGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG T C RNF115 Ensembl:ENSG00000265491 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:145823851..145824033;chr1:145823751..145824327;chr1:145823751..145824187 26863196 MeRIP-seq:(Medium) rs1267084011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072995,Human_RBP_ID_18968765,Human_RBP_ID_22871830 77096 RMVar_ID_77096 Human_SNP_ID_32306646 m1A Human chr1 - 145823916 145823916 145823916 CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGGACGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG CTGCAGCTCGGGAGGTAGCGGCCTGGCGAGGGCCGGGCCGGCTGCCCTCTCGGACGGCCGCGGCG T G RNF115 Ensembl:ENSG00000265491 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:145823851..145824033;chr1:145823751..145824327;chr1:145823751..145824187 26863196 MeRIP-seq:(Medium) rs1267084011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072995,Human_RBP_ID_18968765,Human_RBP_ID_22871830 77097 RMVar_ID_77097 Human_SNP_ID_32308879 m1A Human chr1 + 145831668 145831668 145831668 GAAAGGTATGGACAGAACCCTGACAAAACACCAGGATTACAGTTGGGATCTGAAAGAGGAATCTG GAAAGGTATGGACAGAACCCTGACAAAACACCGGGATTACAGTTGGGATCTGAAAGAGGAATCTG A G POLR3C Ensembl:ENSG00000186141 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:145831663..145831746 26863196 MeRIP-seq:(Medium) rs897039258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10559647 RMVar_hsa_circ_367263,RMVar_hsa_circ_22693,RMVar_hsa_circ_7733,RMVar_hsa_circ_63409 77098 RMVar_ID_77098 Human_SNP_ID_32309021 m1A Human chr1 + 145832332 145832331 145832333 TTGAGAAGCTTGGCTGTGACACTAAGGAAAAGAAGAGAAGGCATAGGGTTGAAAGAGAATTCTAG TTGAGAAGCTTGGCTGTGACACTAAGGAAAAG__GAGAAGGCATAGGGTTGAAAGAGAATTCTAG GAA G POLR3C Ensembl:ENSG00000186141 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:145832327..145832570 26863196 MeRIP-seq:(Medium) rs1247368494 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_367263,RMVar_hsa_circ_22693,RMVar_hsa_circ_7733,RMVar_hsa_circ_63409 77099 RMVar_ID_77099 Human_SNP_ID_32309025 m1A Human chr1 - 145832348 145832348 145832348 CAAGTCTCTTTCTACTCTAGAATTCTCTTTCAACCCTATGCCTTCTCTTCTTTTCCTTAGTGTCA CAAGTCTCTTTCTACTCTAGAATTCTCTTTCAGCCCTATGCCTTCTCTTCTTTTCCTTAGTGTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145832342..145832528 26863196 MeRIP-seq:(Medium) rs1044987032 Functional Loss SNV dbSNP153 33..33 33 - - - 77100 RMVar_ID_77100 Human_SNP_ID_32312434 m1A Human chr1 + 145844477 145844477 145844477 TCAAGAAAATAAAGAATAGATTGGTAGTTACCAGAGGCTAGGAAGGATGGGGAGGATGAAGAGAG TCAAGAAAATAAAGAATAGATTGGTAGTTACCGGAGGCTAGGAAGGATGGGGAGGATGAAGAGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145844448..145844532 26863196 MeRIP-seq:(Medium) rs1299857825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5683548 77101 RMVar_ID_77101 Human_SNP_ID_32314369 m1A Human chr1 + 145849624 145849624 145849624 GGGAGCTCCCCAGCGTGGGGGCCAGTGGGCCCAGAAAGTGAGAAGGGGTCCCTCGGTACTGGAAG GGGAGCTCCCCAGCGTGGGGGCCAGTGGGCCCGGAAAGTGAGAAGGGGTCCCTCGGTACTGGAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:145849512..145849661 32194978 MeRIP-seq:(Medium) rs1553733629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2660898,Human_miRNA_ID_2660899,Human_miRNA_ID_2679351,Human_miRNA_ID_2679352 RMVar_hsa_circ_135812,RMVar_hsa_circ_135820,RMVar_hsa_circ_135822,RMVar_hsa_circ_135813,RMVar_hsa_circ_100723,RMVar_hsa_circ_125752,RMVar_hsa_circ_135811,RMVar_hsa_circ_120514,RMVar_hsa_circ_76044,RMVar_hsa_circ_92509 77102 RMVar_ID_77102 Human_SNP_ID_32314672 m1A Human chr1 - 145850586 145850586 145850586 TGCTGGCTGCCTCAGCTCCTCTCTACCCACAGAGTCCTGACATCTGGCCACCAGCCATCCTCGGT TGCTGGCTGCCTCAGCTCCTCTCTACCCACAGTGTCCTGACATCTGGCCACCAGCCATCCTCGGT T A PIAS3 Ensembl:ENSG00000131788 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:145850536..145850920 32194978 MeRIP-seq:(Medium) rs782510823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_118560,Human_Splice_Rec_118570,Human_Splice_Rec_118598,Human_Splice_Rec_118624 RMVar_hsa_circ_26154,RMVar_hsa_circ_52856,RMVar_hsa_circ_357974 77103 RMVar_ID_77103 Human_SNP_ID_32314673 m1A Human chr1 - 145850586 145850586 145850586 TGCTGGCTGCCTCAGCTCCTCTCTACCCACAGAGTCCTGACATCTGGCCACCAGCCATCCTCGGT TGCTGGCTGCCTCAGCTCCTCTCTACCCACAGCGTCCTGACATCTGGCCACCAGCCATCCTCGGT T G PIAS3 Ensembl:ENSG00000131788 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:145850536..145850920 32194978 MeRIP-seq:(Medium) rs782510823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_118560,Human_Splice_Rec_118570,Human_Splice_Rec_118598,Human_Splice_Rec_118624 RMVar_hsa_circ_26154,RMVar_hsa_circ_52856,RMVar_hsa_circ_357974 77104 RMVar_ID_77104 Human_SNP_ID_32315710 m1A Human chr1 + 145854551 145854551 145854551 TCCTGCAGTCAACTGCCTCACCAGGTACACAGACAAGGAGTAATTCTACTTGGAGGCAGGGGGTA TCCTGCAGTCAACTGCCTCACCAGGTACACAGCCAAGGAGTAATTCTACTTGGAGGCAGGGGGTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:145854502..145854582 26863196 MeRIP-seq:(Medium) rs1553735111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135812,RMVar_hsa_circ_135813,RMVar_hsa_circ_125752,RMVar_hsa_circ_135811,RMVar_hsa_circ_120514,RMVar_hsa_circ_76044,RMVar_hsa_circ_135817,RMVar_hsa_circ_92127,RMVar_hsa_circ_114587,RMVar_hsa_circ_135814,RMVar_hsa_circ_135815 77105 RMVar_ID_77105 Human_SNP_ID_32316463 m1A Human chr1 + 145856897 145856897 145856897 TCATCTGGACACTAGGGGCACAGCTGGACTTCAGGAGGTGCAGAGCCTTGGCCAGGAGCTCGTGC TCATCTGGACACTAGGGGCACAGCTGGACTTCGGGAGGTGCAGAGCCTTGGCCAGGAGCTCGTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:145856848..145856948 32194978 MeRIP-seq:(Medium) rs782683908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96886 RMVar_hsa_circ_125752,RMVar_hsa_circ_135811 77106 RMVar_ID_77106 Human_SNP_ID_32317269 m1A Human chr1 - 145859749 145859747 145859750 CTGGACCGAACTTCTGCCGTGCGGACAGCAGGAGCAGCGCCGAGCCCCATTCCCCCACCTCTCCA CTGGACCGAACTTCTGCCGTGCGGACAGCAG___CAGCGCCGAGCCCCATTCCCCCACCTCTCCA GCTC G PIAS3 Ensembl:ENSG00000131788 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:145859698..145859807 26863196 MeRIP-seq:(Medium) rs1196417185 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3990087 Human_Splice_Rec_118629,Human_Splice_Rec_118657,Human_Splice_Rec_118667 77107 RMVar_ID_77107 Human_SNP_ID_32334307 m1A Human chr1 - 145922232 145922232 145922232 TATTAGAAGTATTATTTTTCTCTTTCCCCCCCACCCCACCCCCAACAGAGTCTGGCTCTGCCGCC TATTAGAAGTATTATTTTTCTCTTTCCCCCCCCCCCCACCCCCAACAGAGTCTGGCTCTGCCGCC T G RBM8A Ensembl:ENSG00000265241 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1380531341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5683483,Human_RBP_ID_8168250 77108 RMVar_ID_77108 Human_SNP_ID_32343219 m1A Human chr1 + 145957917 145957916 145957918 TGCCCACACCAGGCTGCAGCCGCTGCGCTCGCATAGTCTCCATCCCGGCCGCCAATGGAGTAGCG TGCCCACACCAGGCTGCAGCCGCTGCGCTCGC__AGTCTCCATCCCGGCCGCCAATGGAGTAGCG CAT C AC243547.3,LIX1L-AS1 Ensembl:ENSG00000280778,Ensembl:ENSG00000234222 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:145957801..145958002;chr1:145957604..145958025 26863196 MeRIP-seq:(Medium) rs1553760689 Functional Loss DEL dbSNP153 33..34 33 - - - 77109 RMVar_ID_77109 Human_SNP_ID_32344852 m1A Human chr1 - 145964435 145964435 145964435 CGGCGAGAGTTCACCGAGGGAACGTGACACTCATATCTCATCGAGGGACCGTGTTGAGGGAGCCC CGGCGAGAGTTCACCGAGGGAACGTGACACTCGTATCTCATCGAGGGACCGTGTTGAGGGAGCCC T C ANKRD34A Ensembl:ENSG00000272031 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145964388..145964575 26863196 MeRIP-seq:(Medium) rs1423243196 Functional Loss SNV dbSNP153 33..33 33 - - - 77110 RMVar_ID_77110 Human_SNP_ID_32344853 m1A Human chr1 - 145964435 145964435 145964435 CGGCGAGAGTTCACCGAGGGAACGTGACACTCATATCTCATCGAGGGACCGTGTTGAGGGAGCCC CGGCGAGAGTTCACCGAGGGAACGTGACACTCCTATCTCATCGAGGGACCGTGTTGAGGGAGCCC T G ANKRD34A Ensembl:ENSG00000272031 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:145964388..145964575 26863196 MeRIP-seq:(Medium) rs1423243196 Functional Loss SNV dbSNP153 33..33 33 - - - 77111 RMVar_ID_77111 Human_SNP_ID_32347360 m1A Human chr1 - 145974860 145974860 145974860 ACCCCGGCCCCCACCCCGGCTGGCCATGGTGGAGGGGGCCTGGGTATTCAGAGATCCAGTGAATA ACCCCGGCCCCCACCCCGGCTGGCCATGGTGGCGGGGGCCTGGGTATTCAGAGATCCAGTGAATA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:145974832..145974906 26863196 MeRIP-seq:(Medium) rs782705743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265537,RMVar_hsa_circ_135806 77112 RMVar_ID_77112 Human_SNP_ID_32348282 m1A Human chr1 + 145978047 145978045 145978048 AGAGGAGGATGAGGAGAAAGAAGAAGAAGAAGAGAAGGAAGAGGAGGAAGAAGAAGAGTATGATG AGAGGAGGATGAGGAGAAAGAAGAAGAAGAA___AAGGAAGAGGAGGAAGAAGAAGAGTATGATG AGAG A POLR3GL Ensembl:ENSG00000121851 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145977971..145978121 26863196 MeRIP-seq:(Medium) rs1553763795 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_190443,Human_RBP_ID_850312,Human_RBP_ID_1438195,Human_RBP_ID_5642415,Human_RBP_ID_9342213,Human_RBP_ID_18410199,Human_RBP_ID_22870931,Human_RBP_ID_23112450,Human_RBP_ID_24541202,Human_RBP_ID_26311705,Human_RBP_ID_27798449 Human_Splice_Rec_119060,Human_Splice_Rec_119061,Human_Splice_Rec_119076,Human_Splice_Rec_119077,Human_Splice_Rec_119085 77113 RMVar_ID_77113 Human_SNP_ID_32348284 m1A Human chr1 + 145978047 145978047 145978047 AGAGGAGGATGAGGAGAAAGAAGAAGAAGAAGAGAAGGAAGAGGAGGAAGAAGAAGAGTATGATG AGAGGAGGATGAGGAGAAAGAAGAAGAAGAAGCGAAGGAAGAGGAGGAAGAAGAAGAGTATGATG A C POLR3GL Ensembl:ENSG00000121851 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145977971..145978121 26863196 MeRIP-seq:(Medium) rs1271826315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190443,Human_RBP_ID_850312,Human_RBP_ID_1438195,Human_RBP_ID_5642415,Human_RBP_ID_9342213,Human_RBP_ID_18410199,Human_RBP_ID_22870931,Human_RBP_ID_23112450,Human_RBP_ID_24541202,Human_RBP_ID_26311705,Human_RBP_ID_27798449 Human_Splice_Rec_119060,Human_Splice_Rec_119061,Human_Splice_Rec_119076,Human_Splice_Rec_119077,Human_Splice_Rec_119085 77114 RMVar_ID_77114 Human_SNP_ID_32348285 m1A Human chr1 + 145978047 145978047 145978047 AGAGGAGGATGAGGAGAAAGAAGAAGAAGAAGAGAAGGAAGAGGAGGAAGAAGAAGAGTATGATG AGAGGAGGATGAGGAGAAAGAAGAAGAAGAAGGGAAGGAAGAGGAGGAAGAAGAAGAGTATGATG A G POLR3GL Ensembl:ENSG00000121851 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145977971..145978121 26863196 MeRIP-seq:(Medium) rs1271826315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190443,Human_RBP_ID_850312,Human_RBP_ID_1438195,Human_RBP_ID_5642415,Human_RBP_ID_9342213,Human_RBP_ID_18410199,Human_RBP_ID_22870931,Human_RBP_ID_23112450,Human_RBP_ID_24541202,Human_RBP_ID_26311705,Human_RBP_ID_27798449 Human_Splice_Rec_119060,Human_Splice_Rec_119061,Human_Splice_Rec_119076,Human_Splice_Rec_119077,Human_Splice_Rec_119085 77115 RMVar_ID_77115 Human_SNP_ID_32348291 m1A Human chr1 + 145978062 145978060 145978063 GAAAGAAGAAGAAGAAGAGAAGGAAGAGGAGGAAGAAGAAGAGTATGATGAAGAAGAACATGAAG GAAAGAAGAAGAAGAAGAGAAGGAAGAGGAG___GAAGAAGAGTATGATGAAGAAGAACATGAAG GGAA G POLR3GL Ensembl:ENSG00000121851 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:145977798..145978115 26863196 MeRIP-seq:(Medium) rs782130123 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_190443,Human_RBP_ID_850312,Human_RBP_ID_1438195,Human_RBP_ID_5642415,Human_RBP_ID_9342213,Human_RBP_ID_9443808,Human_RBP_ID_18410199,Human_RBP_ID_22870931,Human_RBP_ID_23112450,Human_RBP_ID_24541202,Human_RBP_ID_26311705,Human_RBP_ID_27798449 Human_Splice_Rec_119060,Human_Splice_Rec_119061,Human_Splice_Rec_119076,Human_Splice_Rec_119077,Human_Splice_Rec_119085 77116 RMVar_ID_77116 Human_SNP_ID_32348392 m1A Human chr1 + 145978413 145978413 145978413 ATATTTTGACAATGGAGAGGACTTTGGTGGTGACAGTGATGACAATATGGACGAGGCTATATACT ATATTTTGACAATGGAGAGGACTTTGGTGGTGGCAGTGATGACAATATGGACGAGGCTATATACT A G POLR3GL Ensembl:ENSG00000121851 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:145978328..145978445 26863196 MeRIP-seq:(Medium) rs1329495563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190446,Human_RBP_ID_259011,Human_RBP_ID_1438196,Human_RBP_ID_1724452,Human_RBP_ID_9356742,Human_RBP_ID_18410200,Human_RBP_ID_22023730,Human_RBP_ID_22870932,Human_RBP_ID_24541203,Human_RBP_ID_26311708,Human_RBP_ID_26840305,Human_RBP_ID_27798451 Human_Splice_Rec_119062,Human_Splice_Rec_119078,Human_Splice_Rec_119086 77117 RMVar_ID_77117 Human_SNP_ID_32352979 m1A Human chr1 + 145995286 145995286 145995286 CACACCCATATTTTCCTTTGAAGGATGTTCCCAGAGGCCTGTGTCAAGAAAATGAAAATTTTAAA CACACCCATATTTTCCTTTGAAGGATGTTCCCGGAGGCCTGTGTCAAGAAAATGAAAATTTTAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:145995126..145995300 32194978 MeRIP-seq:(Medium) rs917500336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744569,Human_RBP_ID_802305 RMVar_hsa_circ_135798,RMVar_hsa_circ_105767 77118 RMVar_ID_77118 Human_SNP_ID_32363962 m1A Human chr1 + 146035748 146035748 146035748 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAAAGAGTAACATCTTCTTT TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGCTTCCCGGTCAGGGAAAGAGTAACATCTTCTTT A C tRNA-Glu-CTC-1-1,tRNA-Glu-CTC-2-1 RNACentral:URS00004F0321,RNACentral:URS0000635088 tRNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1158140404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324441,Human_RBP_ID_1249903,Human_RBP_ID_1410569,Human_RBP_ID_5252746,Human_RBP_ID_8283860,Human_RBP_ID_8955290,Human_RBP_ID_18428440,Human_RBP_ID_18550204,Human_RBP_ID_22786773,Human_RBP_ID_23121238,Human_RBP_ID_23329046,Human_RBP_ID_27402250 77119 RMVar_ID_77119 Human_SNP_ID_32363963 m1A Human chr1 + 146035748 146035748 146035748 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAAAGAGTAACATCTTCTTT TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGTTTCCCGGTCAGGGAAAGAGTAACATCTTCTTT A T tRNA-Glu-CTC-1-1,tRNA-Glu-CTC-2-1 RNACentral:URS00004F0321,RNACentral:URS0000635088 tRNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1158140404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324441,Human_RBP_ID_1249903,Human_RBP_ID_1410569,Human_RBP_ID_5252746,Human_RBP_ID_8283860,Human_RBP_ID_8955290,Human_RBP_ID_18428440,Human_RBP_ID_18550204,Human_RBP_ID_22786773,Human_RBP_ID_23121238,Human_RBP_ID_23329046,Human_RBP_ID_27402250 77120 RMVar_ID_77120 Human_SNP_ID_32364521 m1A Human chr1 + 146037117 146037117 146037117 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCAGTGTCAGTTTTTCTCTT TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGCTTCCCGGCCAACGCAGTGTCAGTTTTTCTCTT A C tRNA-Gly-TCC-2-1 RNACentral:URS000034AAC2 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1056221294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271765,Human_RBP_ID_324440,Human_RBP_ID_1249901,Human_RBP_ID_1410567,Human_RBP_ID_3279787,Human_RBP_ID_4080387,Human_RBP_ID_5272865,Human_RBP_ID_5412883,Human_RBP_ID_5456198,Human_RBP_ID_5484196,Human_RBP_ID_5899964,Human_RBP_ID_8240118,Human_RBP_ID_8283859,Human_RBP_ID_8955289,Human_RBP_ID_9454823,Human_RBP_ID_10558851,Human_RBP_ID_17724050,Human_RBP_ID_18428439,Human_RBP_ID_18550199,Human_RBP_ID_19183073,Human_RBP_ID_22015471,Human_RBP_ID_22126568,Human_RBP_ID_22779595,Human_RBP_ID_22846169,Human_RBP_ID_23121230,Human_RBP_ID_23329042,Human_RBP_ID_24395274,Human_RBP_ID_26840291,Human_RBP_ID_27166979,Human_RBP_ID_27387298,Human_RBP_ID_27577977 77121 RMVar_ID_77121 Human_SNP_ID_32364522 m1A Human chr1 + 146037117 146037117 146037117 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCAGTGTCAGTTTTTCTCTT TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGGTTCCCGGCCAACGCAGTGTCAGTTTTTCTCTT A G tRNA-Gly-TCC-2-1 RNACentral:URS000034AAC2 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1056221294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271765,Human_RBP_ID_324440,Human_RBP_ID_1249901,Human_RBP_ID_1410567,Human_RBP_ID_3279787,Human_RBP_ID_4080387,Human_RBP_ID_5272865,Human_RBP_ID_5412883,Human_RBP_ID_5456198,Human_RBP_ID_5484196,Human_RBP_ID_5899964,Human_RBP_ID_8240118,Human_RBP_ID_8283859,Human_RBP_ID_8955289,Human_RBP_ID_9454823,Human_RBP_ID_10558851,Human_RBP_ID_17724050,Human_RBP_ID_18428439,Human_RBP_ID_18550199,Human_RBP_ID_19183073,Human_RBP_ID_22015471,Human_RBP_ID_22126568,Human_RBP_ID_22779595,Human_RBP_ID_22846169,Human_RBP_ID_23121230,Human_RBP_ID_23329042,Human_RBP_ID_24395274,Human_RBP_ID_26840291,Human_RBP_ID_27166979,Human_RBP_ID_27387298,Human_RBP_ID_27577977 77122 RMVar_ID_77122 Human_SNP_ID_32364940 m1A Human chr1 + 146038100 146038100 146038100 CTCTGCGTTGTGGCCGCAGCAACCTCGGTTCGAATCCGAGTCACGGCAGGTGGTTCTAACTTGCT CTCTGCGTTGTGGCCGCAGCAACCTCGGTTCGGATCCGAGTCACGGCAGGTGGTTCTAACTTGCT A G tRNA-His-GTG-1-1,tRNA-His-GTG-2-1 RNACentral:URS000044BAE3,RNACentral:URS000067A424 tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1220953554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324437,Human_RBP_ID_970616,Human_RBP_ID_1410564,Human_RBP_ID_8283854,Human_RBP_ID_8955286,Human_RBP_ID_10558839,Human_RBP_ID_17724048,Human_RBP_ID_18550195,Human_RBP_ID_19444690,Human_RBP_ID_22015470,Human_RBP_ID_22126567,Human_RBP_ID_22779594,Human_RBP_ID_22846166,Human_RBP_ID_23121224,Human_RBP_ID_23329036,Human_RBP_ID_24581702,Human_RBP_ID_26840290,Human_RBP_ID_27152737,Human_RBP_ID_27166978,Human_RBP_ID_27387297 77123 RMVar_ID_77123 Human_SNP_ID_32364971 m1A Human chr1 - 146038129 146038129 146038129 TAATTAAAAAAAAAAAAAACCGCCACCCCAGCAAGTTAGAACCACCTGCCGTGACTCGGATTCGA TAATTAAAAAAAAAAAAAACCGCCACCCCAGCCAGTTAGAACCACCTGCCGTGACTCGGATTCGA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:146038003..146038150 26863196 MeRIP-seq:(Medium) rs1553772367 Functional Loss SNV dbSNP153 33..33 33 - - - 77124 RMVar_ID_77124 Human_SNP_ID_32365536 m1A Human chr1 + 146039458 146039458 146039458 ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGAGCCCCACGTTGGGCGCTGTGTTTTTATTTAAC ATGAGACTCTTAATCTCAGGGTCGTGGGTTCGGGCCCCACGTTGGGCGCTGTGTTTTTATTTAAC A G tRNA-Lys-CTT-2-1 RNACentral:URS00001AD596 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1383968097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324434,Human_RBP_ID_1344563,Human_RBP_ID_1410562,Human_RBP_ID_3279784,Human_RBP_ID_4080384,Human_RBP_ID_5273180,Human_RBP_ID_5484194,Human_RBP_ID_5683243,Human_RBP_ID_8240113,Human_RBP_ID_8283849,Human_RBP_ID_8955284,Human_RBP_ID_10558832,Human_RBP_ID_17674856,Human_RBP_ID_17724045,Human_RBP_ID_18550190,Human_RBP_ID_22485727,Human_RBP_ID_23121218,Human_RBP_ID_23329030,Human_RBP_ID_24395273 77125 RMVar_ID_77125 Human_SNP_ID_32376372 m1A Human chr1 - 146065294 146065294 146065294 TGTTTATAGAAGACAGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGT TGTTTATAGAAGACAGGTCAGCTGTCTGGCTCCATGATCTACATTCTGAAGTTGTCTGAAAATGT T G NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1434990824 Functional Loss SNV dbSNP153 33..33 33 - - - 77126 RMVar_ID_77126 Human_SNP_ID_32376448 m1A Human chr1 - 146065476 146065476 146065476 GACAACTGACCTGTCTCCTTCACATAGTCCATATCACCACAAATCACACAACAAAAAGGAGAAGA GACAACTGACCTGTCTCCTTCACATAGTCCATGTCACCACAAATCACACAACAAAAAGGAGAAGA T C NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1332613723 Functional Loss SNV dbSNP153 33..33 33 - - - 77127 RMVar_ID_77127 Human_SNP_ID_32421657 m1A Human chr1 - 146228784 146228784 146228784 CCGCGGCGGCGGCGGCGGAGGAGGCGACCGAGAAGATACCCGCCCTGCGCCCCGCTCTGCTGTGG CCGCGGCGGCGGCGGCGGAGGAGGCGACCGAGGAGATACCCGCCCTGCGCCCCGCTCTGCTGTGG T C NBPF10,NOTCH2NLA Ensembl:ENSG00000271425,Ensembl:ENSG00000264343 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:146228720..146228811 26863196 MeRIP-seq:(Medium) rs1553820493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_119545,Human_Splice_Rec_119589,Human_Splice_Rec_119599 77128 RMVar_ID_77128 Human_SNP_ID_32421795 m1A Human chr1 + 146228926 146228926 146228926 GGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCAGCGCAAATGCCTCGACTCCCCGCGCCCCGAGT GGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCCGCGCAAATGCCTCGACTCCCCGCGCCCCGAGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:146228723..146228976;chr1:146228815..146228950;chr1:146228725..146228976;chr1:146228867..146228975 26863196 MeRIP-seq:(Medium) rs1553820597 Functional Loss SNV dbSNP153 33..33 33 - - - 77129 RMVar_ID_77129 Human_SNP_ID_32421796 m1A Human chr1 + 146228926 146228926 146228926 GGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCAGCGCAAATGCCTCGACTCCCCGCGCCCCGAGT GGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCTGCGCAAATGCCTCGACTCCCCGCGCCCCGAGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:146228723..146228976;chr1:146228815..146228950;chr1:146228725..146228976;chr1:146228867..146228975 26863196 MeRIP-seq:(Medium) rs1553820597 Functional Loss SNV dbSNP153 33..33 33 - - - 77130 RMVar_ID_77130 Human_SNP_ID_32456006 m1A Human chr1 - 146387491 146387491 146387491 CACACTTGAAATGAAATAGTTGAGTCGGGTTTAAAAGGCATTTCAGTAACCATAATATCTGCCCT CACACTTGAAATGAAATAGTTGAGTCGGGTTTTAAAGGCATTTCAGTAACCATAATATCTGCCCT T A SEC22B4P Ensembl:ENSG00000277406 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:146387470..146387626 26863196 MeRIP-seq:(Medium) rs1252349251 Functional Loss SNV dbSNP153 33..33 33 - - - 77131 RMVar_ID_77131 Human_SNP_ID_32456009 m1A Human chr1 + 146387493 146387493 146387493 GGCAGATATTATGGTTACTGAAATGCCTTTTAAACCCGACTCAACTATTTCATTTCAAGTGTGCT GGCAGATATTATGGTTACTGAAATGCCTTTTACACCCGACTCAACTATTTCATTTCAAGTGTGCT A C AC245407.2 Ensembl:ENSG00000287978 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:146387472..146387610 26863196 MeRIP-seq:(Medium) rs1240163875 Functional Loss SNV dbSNP153 33..33 33 - - - 77132 RMVar_ID_77132 Human_SNP_ID_32456066 m1A Human chr1 - 146387540 146387540 146387540 TACAAATTACACAGCTGAGCTTCCCACCTTGGAGAAAATGACAGAACAGCACACTTGAAATGAAA TACAAATTACACAGCTGAGCTTCCCACCTTGGGGAAAATGACAGAACAGCACACTTGAAATGAAA T C SEC22B4P Ensembl:ENSG00000277406 Pseudogene intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:146387536..146387623 26863410 MeRIP-seq:(Medium) rs1402123356 Functional Loss SNV dbSNP153 33..33 33 - - - 77133 RMVar_ID_77133 Human_SNP_ID_32456067 m1A Human chr1 - 146387540 146387540 146387540 TACAAATTACACAGCTGAGCTTCCCACCTTGGAGAAAATGACAGAACAGCACACTTGAAATGAAA TACAAATTACACAGCTGAGCTTCCCACCTTGGCGAAAATGACAGAACAGCACACTTGAAATGAAA T G SEC22B4P Ensembl:ENSG00000277406 Pseudogene intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:146387536..146387623 26863410 MeRIP-seq:(Medium) rs1402123356 Functional Loss SNV dbSNP153 33..33 33 - - - 77134 RMVar_ID_77134 Human_SNP_ID_32456226 m1A Human chr1 + 146387644 146387644 146387644 TGTGCTTGGCAGGGCCCCCCTCCCCCCCACCAAGGCCTGCAGTGGATAGAGCCTAGCAGATCCTG TGTGCTTGGCAGGGCCCCCCTCCCCCCCACCAGGGCCTGCAGTGGATAGAGCCTAGCAGATCCTG A G AC245407.2 Ensembl:ENSG00000287978 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:146387548..146387661 26863196 MeRIP-seq:(Medium) rs1340810174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_119620 77135 RMVar_ID_77135 Human_SNP_ID_32461387 m1A Human chr1 - 146409944 146409944 146409944 ACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGGCCGTATTTTCTCCTGTTA ACTGAGTACAATGGAGAAATCGCCCCCGAAAATCACCAACTTCATGGCCGTATTTTCTCCTGTTA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:146409942..146410080 26863196 MeRIP-seq:(Medium) rs1168226521 Functional Loss SNV dbSNP153 33..33 33 - - - 77136 RMVar_ID_77136 Human_SNP_ID_32461388 m1A Human chr1 - 146409944 146409944 146409944 ACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGGCCGTATTTTCTCCTGTTA ACTGAGTACAATGGAGAAATCGCCCCCGAAAAGCACCAACTTCATGGCCGTATTTTCTCCTGTTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:146409942..146410080 26863196 MeRIP-seq:(Medium) rs1168226521 Functional Loss SNV dbSNP153 33..33 33 - - - 77137 RMVar_ID_77137 Human_SNP_ID_32461389 m1A Human chr1 - 146409944 146409944 146409944 ACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGGCCGTATTTTCTCCTGTTA ACTGAGTACAATGGAGAAATCGCCCCCGAAAACCACCAACTTCATGGCCGTATTTTCTCCTGTTA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:146409942..146410080 26863196 MeRIP-seq:(Medium) rs1168226521 Functional Loss SNV dbSNP153 33..33 33 - - - 77138 RMVar_ID_77138 Human_SNP_ID_32461392 m1A Human chr1 - 146409947 146409947 146409947 CATACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGGCCGTATTTTCTCCTG CATACTGAGTACAATGGAGAAATCGCCCCCGAGAAACACCAACTTCATGGCCGTATTTTCTCCTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:146409918..146410046 26863196 MeRIP-seq:(Medium) rs1258887559 Functional Loss SNV dbSNP153 33..33 33 - - - 77139 RMVar_ID_77139 Human_SNP_ID_32461393 m1A Human chr1 - 146409947 146409947 146409947 CATACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGGCCGTATTTTCTCCTG CATACTGAGTACAATGGAGAAATCGCCCCCGACAAACACCAACTTCATGGCCGTATTTTCTCCTG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:146409918..146410046 26863196 MeRIP-seq:(Medium) rs1258887559 Functional Loss SNV dbSNP153 33..33 33 - - - 77140 RMVar_ID_77140 Human_SNP_ID_32461413 m1A Human chr1 - 146409962 146409962 146409962 AGGAGTCAGTCAGCACATACTGAGTACAATGGAGAAATCGCCCCCGAAAAACACCAACTTCATGG AGGAGTCAGTCAGCACATACTGAGTACAATGGGGAAATCGCCCCCGAAAAACACCAACTTCATGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:146409901..146409975 26863196 MeRIP-seq:(Medium) rs1178202694 Functional Loss SNV dbSNP153 33..33 33 - - - 77141 RMVar_ID_77141 Human_SNP_ID_32474428 m1A Human chr1 + 146472613 146472613 146472613 GCCGAGCGGGACCCTGAGGAGCCAGCTGGCGCAGGCTATGGGCTGGGCGGCGGTTGAGACAGCGG GCCGAGCGGGACCCTGAGGAGCCAGCTGGCGCGGGCTATGGGCTGGGCGGCGGTTGAGACAGCGG A G HYDIN2 Ensembl:ENSG00000276975 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:146472579..146472672 26863196 MeRIP-seq:(Medium) rs1466698315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_119623 77142 RMVar_ID_77142 Human_SNP_ID_32624046 m1A Human chr1 - 147172135 147172133 147172135 GTGGTCCCCGACGAGCTGCAGCCATGGGAAACACCACCAGCGACCGGGTGTCCGGGGAGCGCCAC GTGGTCCCCGACGAGCTGCAGCCATGGGAAAC__CACCAGCGACCGGGTGTCCGGGGAGCGCCAC GGT G PRKAB2 Ensembl:ENSG00000131791 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:147172040..147172451 26863410 MeRIP-seq:(Medium) rs1553914551 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3990328,Human_RBP_ID_18550389,Human_RBP_ID_19035261,Human_RBP_ID_24582247 Human_Splice_Rec_120248,Human_Splice_Rec_120268 RMVar_hsa_circ_81391,RMVar_hsa_circ_135841 77143 RMVar_ID_77143 Human_SNP_ID_32624049 m1A Human chr1 - 147172135 147172135 147172135 GTGGTCCCCGACGAGCTGCAGCCATGGGAAACACCACCAGCGACCGGGTGTCCGGGGAGCGCCAC GTGGTCCCCGACGAGCTGCAGCCATGGGAAACGCCACCAGCGACCGGGTGTCCGGGGAGCGCCAC T C PRKAB2 Ensembl:ENSG00000131791 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:147172040..147172451 26863410 MeRIP-seq:(Medium) rs782609266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3990328,Human_RBP_ID_18550389,Human_RBP_ID_19035261,Human_RBP_ID_24582247 Human_Splice_Rec_120248,Human_Splice_Rec_120268 RMVar_hsa_circ_81391,RMVar_hsa_circ_135841 77144 RMVar_ID_77144 Human_SNP_ID_32624149 m1A Human chr1 - 147172430 147172430 147172430 AGTGGCCCTTGGAGGAGGGAGCGCATCGCCCGAGGTGACTGGAGTGGGGGCGCCCCTGGCAGTGA AGTGGCCCTTGGAGGAGGGAGCGCATCGCCCGGGGTGACTGGAGTGGGGGCGCCCCTGGCAGTGA T C PRKAB2 Ensembl:ENSG00000131791 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:147172057..147172574 26863196 MeRIP-seq:(Medium) rs1308312299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803393 Human_Splice_Rec_120247,Human_Splice_Rec_120267 RMVar_hsa_circ_81391,RMVar_hsa_circ_135841 77145 RMVar_ID_77145 Human_SNP_ID_32624295 m1A Human chr1 + 147172900 147172900 147172900 CCGCCTCAGGTGCGCCAGCACGTTTTCTGGGCAGCATCTGTGTGTTAGGCGACCGGAGAGGTGGG CCGCCTCAGGTGCGCCAGCACGTTTTCTGGGCCGCATCTGTGTGTTAGGCGACCGGAGAGGTGGG A C PDIA3P1,AC242426.2 Ensembl:ENSG00000180867,Ensembl:ENSG00000237188 Pseudogene,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147172849..147172932 26863196 MeRIP-seq:(Medium) rs1246014852 Functional Loss SNV dbSNP153 33..33 33 - - - 77146 RMVar_ID_77146 Human_SNP_ID_32631763 m1A Human chr1 - 147203893 147203893 147203893 ACACCTCCTGTCCTTGAAGAAATGGGACACTGAGACAGTGTTTACCTCTCAGAAGTTGGAGATAC ACACCTCCTGTCCTTGAAGAAATGGGACACTGTGACAGTGTTTACCTCTCAGAAGTTGGAGATAC T A CCT8P1,FMO5 Ensembl:ENSG00000226015,Ensembl:ENSG00000131781 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879998874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1827667,Human_miRNA_ID_1838291,Human_miRNA_ID_1851327,Human_miRNA_ID_1851459,Human_miRNA_ID_1851591,Human_miRNA_ID_1851723,Human_miRNA_ID_1851855 RMVar_hsa_circ_70581,RMVar_hsa_circ_339476,RMVar_hsa_circ_353641,RMVar_hsa_circ_350838,RMVar_hsa_circ_71401,RMVar_hsa_circ_362994,RMVar_hsa_circ_357139 77147 RMVar_ID_77147 Human_SNP_ID_32641680 m1A Human chr1 + 147242767 147242767 147242767 GCCAAGCCCCTGGCTTCTTACTGCGGCTTCATACTGAGGGCCGAGCCGAGGCGGCGCGGGTGCAG GCCAAGCCCCTGGCTTCTTACTGCGGCTTCATGCTGAGGGCCGAGCCGAGGCGGCGCGGGTGCAG A G CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:147242717..147242883 26863196 MeRIP-seq:(Medium) rs1351011184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324841,Human_RBP_ID_970744,Human_RBP_ID_3936499,Human_RBP_ID_3990416,Human_RBP_ID_5109182,Human_RBP_ID_5542083,Human_RBP_ID_8754099,Human_RBP_ID_9270302,Human_RBP_ID_9319105,Human_RBP_ID_17646515,Human_RBP_ID_18157813,Human_RBP_ID_18415045,Human_RBP_ID_18428458,Human_RBP_ID_18968798,Human_RBP_ID_22126685,Human_RBP_ID_26840438 Human_Splice_Rec_120453,Human_Splice_Rec_120475,Human_Splice_Rec_120515,Human_Splice_Rec_120551,Human_Splice_Rec_120593,Human_Splice_Rec_120633,Human_Splice_Rec_120671,Human_Splice_Rec_120709,Human_Splice_Rec_120749,Human_Splice_Rec_120781,Human_Splice_Rec_120819,Human_Splice_Rec_120863,Human_Splice_Rec_120901,Human_Splice_Rec_120943,Human_Splice_Rec_120975,Human_Splice_Rec_121017,Human_Splice_Rec_121059,Human_Splice_Rec_121101,Human_Splice_Rec_121135,Human_Splice_Rec_121173,Human_Splice_Rec_121213,Human_Splice_Rec_121251,Human_Splice_Rec_121291,Human_Splice_Rec_121331,Human_Splice_Rec_121365,Human_Splice_Rec_121405,Human_Splice_Rec_121445,Human_Splice_Rec_121463,Human_Splice_Rec_121507 77148 RMVar_ID_77148 Human_SNP_ID_32641681 m1A Human chr1 - 147242769 147242769 147242769 TCCTGCACCCGCGCCGCCTCGGCTCGGCCCTCAGTATGAAGCCGCAGTAAGAAGCCAGGGGCTTG TCCTGCACCCGCGCCGCCTCGGCTCGGCCCTCTGTATGAAGCCGCAGTAAGAAGCCAGGGGCTTG T A FMO5 Ensembl:ENSG00000131781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147242719..147242894 26863196 MeRIP-seq:(Medium) rs782715735 Functional Loss SNV dbSNP153 33..33 33 - - - 77149 RMVar_ID_77149 Human_SNP_ID_32641682 m1A Human chr1 - 147242769 147242769 147242769 TCCTGCACCCGCGCCGCCTCGGCTCGGCCCTCAGTATGAAGCCGCAGTAAGAAGCCAGGGGCTTG TCCTGCACCCGCGCCGCCTCGGCTCGGCCCTCGGTATGAAGCCGCAGTAAGAAGCCAGGGGCTTG T C FMO5 Ensembl:ENSG00000131781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147242719..147242894 26863196 MeRIP-seq:(Medium) rs782715735 Functional Loss SNV dbSNP153 33..33 33 - - - 77150 RMVar_ID_77150 Human_SNP_ID_32644090 m1A Human chr1 - 147252575 147252575 147252575 ACAGCAAATCCGAAGAGCAGACATTTCAGTACATGCAGAGGCAATGTTCTAAGAGTTTGAATGAG ACAGCAAATCCGAAGAGCAGACATTTCAGTACGTGCAGAGGCAATGTTCTAAGAGTTTGAATGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147252573..147252659 26863196 MeRIP-seq:(Medium) rs782759050 Functional Loss SNV dbSNP153 33..33 33 - - - 77151 RMVar_ID_77151 Human_SNP_ID_32644091 m1A Human chr1 - 147252575 147252575 147252575 ACAGCAAATCCGAAGAGCAGACATTTCAGTACATGCAGAGGCAATGTTCTAAGAGTTTGAATGAG ACAGCAAATCCGAAGAGCAGACATTTCAGTACCTGCAGAGGCAATGTTCTAAGAGTTTGAATGAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147252573..147252659 26863196 MeRIP-seq:(Medium) rs782759050 Functional Loss SNV dbSNP153 33..33 33 - - - 77152 RMVar_ID_77152 Human_SNP_ID_32648377 m1A Human chr1 + 147268815 147268815 147268815 TGTGGAGCCGGAGCCTTTTGAAGTTGGAGACCACCTGACTGAGGCTAGTGGGAAGCTTCACCTGC TGTGGAGCCGGAGCCTTTTGAAGTTGGAGACCCCCTGACTGAGGCTAGTGGGAAGCTTCACCTGC A C CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:147267427..147270914 32194978 MeRIP-seq:(Medium) rs781839697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19723,Human_RBP_ID_855135,Human_RBP_ID_3990446,Human_RBP_ID_5335790,Human_RBP_ID_8754100,Human_RBP_ID_9270303,Human_RBP_ID_9342958,Human_RBP_ID_9356752,Human_RBP_ID_10562787,Human_RBP_ID_18968805,Human_RBP_ID_19035270,Human_RBP_ID_22535430,Human_RBP_ID_22634210,Human_RBP_ID_24746890,Human_RBP_ID_26309797 Human_Splice_Rec_120290,Human_Splice_Rec_120291,Human_Splice_Rec_120488,Human_Splice_Rec_120489,Human_Splice_Rec_120526,Human_Splice_Rec_120527,Human_Splice_Rec_120566,Human_Splice_Rec_120567,Human_Splice_Rec_120608,Human_Splice_Rec_120609,Human_Splice_Rec_120644,Human_Splice_Rec_120645,Human_Splice_Rec_120684,Human_Splice_Rec_120685,Human_Splice_Rec_120722,Human_Splice_Rec_120723,Human_Splice_Rec_120754,Human_Splice_Rec_120755,Human_Splice_Rec_120794,Human_Splice_Rec_120795,Human_Splice_Rec_120836,Human_Splice_Rec_120837,Human_Splice_Rec_120878,Human_Splice_Rec_120879,Human_Splice_Rec_120916,Human_Splice_Rec_120917,Human_Splice_Rec_120948,Human_Splice_Rec_120949,Human_Splice_Rec_120990,Human_Splice_Rec_120991,Human_Splice_Rec_121032,Human_Splice_Rec_121033,Human_Splice_Rec_121074,Human_Splice_Rec_121075,Human_Splice_Rec_121108,Human_Splice_Rec_121109,Human_Splice_Rec_121150,Human_Splice_Rec_121151,Human_Splice_Rec_121188,Human_Splice_Rec_121189,Human_Splice_Rec_121224,Human_Splice_Rec_121225,Human_Splice_Rec_121264,Human_Splice_Rec_121265,Human_Splice_Rec_121304,Human_Splice_Rec_121305,Human_Splice_Rec_121338,Human_Splice_Rec_121339,Human_Splice_Rec_121378,Human_Splice_Rec_121379,Human_Splice_Rec_121420,Human_Splice_Rec_121421,Human_Splice_Rec_121460,Human_Splice_Rec_121461,Human_Splice_Rec_121478,Human_Splice_Rec_121479,Human_Splice_Rec_121532,Human_Splice_Rec_121533,Human_Splice_Rec_121572,Human_Splice_Rec_121573,Human_Splice_Rec_121602,Human_Splice_Rec_121603 RMVar_hsa_circ_15914,RMVar_hsa_circ_308605,RMVar_hsa_circ_353752,RMVar_hsa_circ_366447,RMVar_hsa_circ_277269,RMVar_hsa_circ_28439,RMVar_hsa_circ_19792,RMVar_hsa_circ_324782,RMVar_hsa_circ_40764,RMVar_hsa_circ_71329,RMVar_hsa_circ_353505,RMVar_hsa_circ_71510,RMVar_hsa_circ_10932,RMVar_hsa_circ_15963,RMVar_hsa_circ_361423,RMVar_hsa_circ_287873,RMVar_hsa_circ_2767,RMVar_hsa_circ_3070,RMVar_hsa_circ_70012,RMVar_hsa_circ_48941,RMVar_hsa_circ_135842,RMVar_hsa_circ_334643,RMVar_hsa_circ_71690 77153 RMVar_ID_77153 Human_SNP_ID_32648378 m1A Human chr1 + 147268815 147268815 147268815 TGTGGAGCCGGAGCCTTTTGAAGTTGGAGACCACCTGACTGAGGCTAGTGGGAAGCTTCACCTGC TGTGGAGCCGGAGCCTTTTGAAGTTGGAGACCGCCTGACTGAGGCTAGTGGGAAGCTTCACCTGC A G CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:147267427..147270914 32194978 MeRIP-seq:(Medium) rs781839697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19723,Human_RBP_ID_855135,Human_RBP_ID_3990446,Human_RBP_ID_5335790,Human_RBP_ID_8754100,Human_RBP_ID_9270303,Human_RBP_ID_9342958,Human_RBP_ID_9356752,Human_RBP_ID_10562787,Human_RBP_ID_18968805,Human_RBP_ID_19035270,Human_RBP_ID_22535430,Human_RBP_ID_22634210,Human_RBP_ID_24746890,Human_RBP_ID_26309797 Human_Splice_Rec_120290,Human_Splice_Rec_120291,Human_Splice_Rec_120488,Human_Splice_Rec_120489,Human_Splice_Rec_120526,Human_Splice_Rec_120527,Human_Splice_Rec_120566,Human_Splice_Rec_120567,Human_Splice_Rec_120608,Human_Splice_Rec_120609,Human_Splice_Rec_120644,Human_Splice_Rec_120645,Human_Splice_Rec_120684,Human_Splice_Rec_120685,Human_Splice_Rec_120722,Human_Splice_Rec_120723,Human_Splice_Rec_120754,Human_Splice_Rec_120755,Human_Splice_Rec_120794,Human_Splice_Rec_120795,Human_Splice_Rec_120836,Human_Splice_Rec_120837,Human_Splice_Rec_120878,Human_Splice_Rec_120879,Human_Splice_Rec_120916,Human_Splice_Rec_120917,Human_Splice_Rec_120948,Human_Splice_Rec_120949,Human_Splice_Rec_120990,Human_Splice_Rec_120991,Human_Splice_Rec_121032,Human_Splice_Rec_121033,Human_Splice_Rec_121074,Human_Splice_Rec_121075,Human_Splice_Rec_121108,Human_Splice_Rec_121109,Human_Splice_Rec_121150,Human_Splice_Rec_121151,Human_Splice_Rec_121188,Human_Splice_Rec_121189,Human_Splice_Rec_121224,Human_Splice_Rec_121225,Human_Splice_Rec_121264,Human_Splice_Rec_121265,Human_Splice_Rec_121304,Human_Splice_Rec_121305,Human_Splice_Rec_121338,Human_Splice_Rec_121339,Human_Splice_Rec_121378,Human_Splice_Rec_121379,Human_Splice_Rec_121420,Human_Splice_Rec_121421,Human_Splice_Rec_121460,Human_Splice_Rec_121461,Human_Splice_Rec_121478,Human_Splice_Rec_121479,Human_Splice_Rec_121532,Human_Splice_Rec_121533,Human_Splice_Rec_121572,Human_Splice_Rec_121573,Human_Splice_Rec_121602,Human_Splice_Rec_121603 RMVar_hsa_circ_15914,RMVar_hsa_circ_308605,RMVar_hsa_circ_353752,RMVar_hsa_circ_366447,RMVar_hsa_circ_277269,RMVar_hsa_circ_28439,RMVar_hsa_circ_19792,RMVar_hsa_circ_324782,RMVar_hsa_circ_40764,RMVar_hsa_circ_71329,RMVar_hsa_circ_353505,RMVar_hsa_circ_71510,RMVar_hsa_circ_10932,RMVar_hsa_circ_15963,RMVar_hsa_circ_361423,RMVar_hsa_circ_287873,RMVar_hsa_circ_2767,RMVar_hsa_circ_3070,RMVar_hsa_circ_70012,RMVar_hsa_circ_48941,RMVar_hsa_circ_135842,RMVar_hsa_circ_334643,RMVar_hsa_circ_71690 77154 RMVar_ID_77154 Human_SNP_ID_32653303 m1A Human chr1 + 147285427 147285427 147285427 CAGACAGAAGAAAAGACAAGAAGCAGCTGCCAAGAGAAGGAGACTCATAGAGGAGAAGAAGAGGC CAGACAGAAGAAAAGACAAGAAGCAGCTGCCAGGAGAAGGAGACTCATAGAGGAGAAGAAGAGGC A G CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA CDS,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147285351..147285530 26863196 MeRIP-seq:(Medium) rs782707976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19732,Human_RBP_ID_855139,Human_RBP_ID_5536440,Human_RBP_ID_17724380,Human_RBP_ID_22023743,Human_RBP_ID_22846318,Human_RBP_ID_24541204,Human_RBP_ID_26314602 Human_Splice_Rec_120303,Human_Splice_Rec_120337,Human_Splice_Rec_120463,Human_Splice_Rec_120503,Human_Splice_Rec_120539,Human_Splice_Rec_120581,Human_Splice_Rec_120621,Human_Splice_Rec_120659,Human_Splice_Rec_120697,Human_Splice_Rec_120737,Human_Splice_Rec_120769,Human_Splice_Rec_120807,Human_Splice_Rec_120851,Human_Splice_Rec_120889,Human_Splice_Rec_120931,Human_Splice_Rec_120963,Human_Splice_Rec_121005,Human_Splice_Rec_121047,Human_Splice_Rec_121089,Human_Splice_Rec_121123,Human_Splice_Rec_121161,Human_Splice_Rec_121201,Human_Splice_Rec_121239,Human_Splice_Rec_121279,Human_Splice_Rec_121319,Human_Splice_Rec_121353,Human_Splice_Rec_121393,Human_Splice_Rec_121433,Human_Splice_Rec_121493,Human_Splice_Rec_121545,Human_Splice_Rec_121587,Human_Splice_Rec_121615 RMVar_hsa_circ_366447,RMVar_hsa_circ_28439,RMVar_hsa_circ_40764,RMVar_hsa_circ_71329,RMVar_hsa_circ_361423,RMVar_hsa_circ_70012,RMVar_hsa_circ_71690,RMVar_hsa_circ_327337,RMVar_hsa_circ_74942,RMVar_hsa_circ_60547,RMVar_hsa_circ_62537,RMVar_hsa_circ_71701,RMVar_hsa_circ_355145,RMVar_hsa_circ_270045,RMVar_hsa_circ_59670 77155 RMVar_ID_77155 Human_SNP_ID_32653321 m1A Human chr1 + 147285454 147285452 147285454 TGCCAAGAGAAGGAGACTCATAGAGGAGAAGAAGAGGCAAAAGGAAGAGGCTGAACATAAGAAAA TGCCAAGAGAAGGAGACTCATAGAGGAGAAG__GAGGCAAAAGGAAGAGGCTGAACATAAGAAAA GAA G CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:147285326..147285523 26863196 MeRIP-seq:(Medium) rs1559876900 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_855139,Human_RBP_ID_2092003,Human_RBP_ID_3933891,Human_RBP_ID_5519146,Human_RBP_ID_5536440,Human_RBP_ID_5684405,Human_RBP_ID_9342960,Human_RBP_ID_24541204,Human_RBP_ID_26314602,Human_RBP_ID_27798457 Human_Splice_Rec_120303,Human_Splice_Rec_120337,Human_Splice_Rec_120463,Human_Splice_Rec_120503,Human_Splice_Rec_120539,Human_Splice_Rec_120581,Human_Splice_Rec_120621,Human_Splice_Rec_120659,Human_Splice_Rec_120697,Human_Splice_Rec_120737,Human_Splice_Rec_120769,Human_Splice_Rec_120807,Human_Splice_Rec_120851,Human_Splice_Rec_120889,Human_Splice_Rec_120931,Human_Splice_Rec_120963,Human_Splice_Rec_121005,Human_Splice_Rec_121047,Human_Splice_Rec_121089,Human_Splice_Rec_121123,Human_Splice_Rec_121161,Human_Splice_Rec_121201,Human_Splice_Rec_121239,Human_Splice_Rec_121279,Human_Splice_Rec_121319,Human_Splice_Rec_121353,Human_Splice_Rec_121393,Human_Splice_Rec_121433,Human_Splice_Rec_121493,Human_Splice_Rec_121545,Human_Splice_Rec_121587,Human_Splice_Rec_121615 RMVar_hsa_circ_366447,RMVar_hsa_circ_28439,RMVar_hsa_circ_40764,RMVar_hsa_circ_71329,RMVar_hsa_circ_361423,RMVar_hsa_circ_70012,RMVar_hsa_circ_71690,RMVar_hsa_circ_327337,RMVar_hsa_circ_74942,RMVar_hsa_circ_60547,RMVar_hsa_circ_62537,RMVar_hsa_circ_71701,RMVar_hsa_circ_355145,RMVar_hsa_circ_270045,RMVar_hsa_circ_59670 77156 RMVar_ID_77156 Human_SNP_ID_32653322 m1A Human chr1 + 147285454 147285454 147285454 TGCCAAGAGAAGGAGACTCATAGAGGAGAAGAAGAGGCAAAAGGAAGAGGCTGAACATAAGAAAA TGCCAAGAGAAGGAGACTCATAGAGGAGAAGAGGAGGCAAAAGGAAGAGGCTGAACATAAGAAAA A G CHD1L,AC242426.2 Ensembl:ENSG00000131778,Ensembl:ENSG00000237188 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:147285326..147285523 26863196 MeRIP-seq:(Medium) rs369368487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855139,Human_RBP_ID_2092003,Human_RBP_ID_3933891,Human_RBP_ID_5519146,Human_RBP_ID_5536440,Human_RBP_ID_5684405,Human_RBP_ID_9342960,Human_RBP_ID_24541204,Human_RBP_ID_26314602,Human_RBP_ID_27798457 Human_Splice_Rec_120303,Human_Splice_Rec_120337,Human_Splice_Rec_120463,Human_Splice_Rec_120503,Human_Splice_Rec_120539,Human_Splice_Rec_120581,Human_Splice_Rec_120621,Human_Splice_Rec_120659,Human_Splice_Rec_120697,Human_Splice_Rec_120737,Human_Splice_Rec_120769,Human_Splice_Rec_120807,Human_Splice_Rec_120851,Human_Splice_Rec_120889,Human_Splice_Rec_120931,Human_Splice_Rec_120963,Human_Splice_Rec_121005,Human_Splice_Rec_121047,Human_Splice_Rec_121089,Human_Splice_Rec_121123,Human_Splice_Rec_121161,Human_Splice_Rec_121201,Human_Splice_Rec_121239,Human_Splice_Rec_121279,Human_Splice_Rec_121319,Human_Splice_Rec_121353,Human_Splice_Rec_121393,Human_Splice_Rec_121433,Human_Splice_Rec_121493,Human_Splice_Rec_121545,Human_Splice_Rec_121587,Human_Splice_Rec_121615 RMVar_hsa_circ_366447,RMVar_hsa_circ_28439,RMVar_hsa_circ_40764,RMVar_hsa_circ_71329,RMVar_hsa_circ_361423,RMVar_hsa_circ_70012,RMVar_hsa_circ_71690,RMVar_hsa_circ_327337,RMVar_hsa_circ_74942,RMVar_hsa_circ_60547,RMVar_hsa_circ_62537,RMVar_hsa_circ_71701,RMVar_hsa_circ_355145,RMVar_hsa_circ_270045,RMVar_hsa_circ_59670 77157 RMVar_ID_77157 Human_SNP_ID_32743592 m1A Human chr1 + 147599561 147599561 147599561 GCGGGAAGGTCCGGGAGAGTGAGCGCGTGGGGAGGAGGGGACGGGAAGAGGAGACCCTCCCGTGC GCGGGAAGGTCCGGGAGAGTGAGCGCGTGGGGCGGAGGGGACGGGAAGAGGAGACCCTCCCGTGC A C BCL9 Ensembl:ENSG00000116128 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:147599439..147599571 26863196 MeRIP-seq:(Medium) rs1399802587 Functional Loss SNV dbSNP153 33..33 33 - - - 77158 RMVar_ID_77158 Human_SNP_ID_32743874 m1A Human chr1 + 147600186 147600186 147600186 CAATGGAGCCTATGTGTGCTTGCCGGAGTGGGACGGCGCCGCCGCCGCCGCTGCCGCCGCCGGGG CAATGGAGCCTATGTGTGCTTGCCGGAGTGGGCCGGCGCCGCCGCCGCCGCTGCCGCCGCCGGGG A C BCL9 Ensembl:ENSG00000116128 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:147600146..147600382 26863196 MeRIP-seq:(Medium) rs1379906731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3990538,Human_RBP_ID_5456218 77159 RMVar_ID_77159 Human_SNP_ID_32846170 m1A Human chr1 + 148038802 148038802 148038802 GCAGTCCCCCACTACCACAAATTATGCAGTCGAGTTTCCCACATTTGGGGAAATCGCAGGGGTCA GCAGTCCCCCACTACCACAAATTATGCAGTCGGGTTTCCCACATTTGGGGAAATCGCAGGGGTCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:148038751..148038825 26863196 MeRIP-seq:(Medium) rs1426597070 Functional Loss SNV dbSNP153 33..33 33 - - - 77160 RMVar_ID_77160 Human_SNP_ID_32846244 m1A Human chr1 - 148038852 148038852 148038852 CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCATTGCACTCCGGATGTGCTGACCCCTGCGATTT CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCTTTGCACTCCGGATGTGCTGACCCCTGCGATTT T A RNVU1-7 Ensembl:ENSG00000206585 snRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1244932398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9553435,Human_RBP_ID_17341662,Human_RBP_ID_18174109,Human_RBP_ID_18198197,Human_RBP_ID_18205147,Human_RBP_ID_18236451,Human_RBP_ID_23112773,Human_RBP_ID_23117752,Human_RBP_ID_24550637,Human_RBP_ID_26747145,Human_RBP_ID_26872581 Human_miRNA_ID_3127866,Human_miRNA_ID_3127973,Human_miRNA_ID_3131544,Human_miRNA_ID_3131622,Human_miRNA_ID_3135070,Human_miRNA_ID_3136814,Human_miRNA_ID_3137325 77161 RMVar_ID_77161 Human_SNP_ID_32846245 m1A Human chr1 - 148038852 148038852 148038852 CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCATTGCACTCCGGATGTGCTGACCCCTGCGATTT CGAAGGTGGTTTTCCCAGGGCGAGGCTTATCCGTTGCACTCCGGATGTGCTGACCCCTGCGATTT T C RNVU1-7 Ensembl:ENSG00000206585 snRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1244932398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9553435,Human_RBP_ID_17341662,Human_RBP_ID_18174109,Human_RBP_ID_18198197,Human_RBP_ID_18205147,Human_RBP_ID_18236451,Human_RBP_ID_23112773,Human_RBP_ID_23117752,Human_RBP_ID_24550637,Human_RBP_ID_26747145,Human_RBP_ID_26872581 Human_miRNA_ID_3127866,Human_miRNA_ID_3127973,Human_miRNA_ID_3131544,Human_miRNA_ID_3131622,Human_miRNA_ID_3135070,Human_miRNA_ID_3136814,Human_miRNA_ID_3137325 77162 RMVar_ID_77162 Human_SNP_ID_32877966 m1A Human chr1 - 148152187 148152187 148152187 TGGCAGGGGCGGTTCAAGTGGCCGGGGAAATCAGCGAATTGCAGGGTCAAGGGCTGGTGCTTTGA TGGCAGGGGCGGTTCAAGTGGCCGGGGAAATCGGCGAATTGCAGGGTCAAGGGCTGGTGCTTTGA T C NBPF11 Ensembl:ENSG00000263956 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:148152145..148152260 26863196 MeRIP-seq:(Medium) rs2746923 Functional Loss SNV dbSNP153 33..33 33 - - - 77163 RMVar_ID_77163 Human_SNP_ID_32877967 m1A Human chr1 - 148152187 148152187 148152187 TGGCAGGGGCGGTTCAAGTGGCCGGGGAAATCAGCGAATTGCAGGGTCAAGGGCTGGTGCTTTGA TGGCAGGGGCGGTTCAAGTGGCCGGGGAAATCCGCGAATTGCAGGGTCAAGGGCTGGTGCTTTGA T G NBPF11 Ensembl:ENSG00000263956 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:148152145..148152260 26863196 MeRIP-seq:(Medium) rs2746923 Functional Loss SNV dbSNP153 33..33 33 - - - 77164 RMVar_ID_77164 Human_SNP_ID_32912757 m1A Human chr1 - 148308937 148308937 148308937 TTCGGTGCTTTCACCCGTGCGGCCCGGGTTCAATTCCCGATGAAGGAATACATTTTGTAACATCC TTCGGTGCTTTCACCCGTGCGGCCCGGGTTCATTTCCCGATGAAGGAATACATTTTGTAACATCC T A LINC01138 Ensembl:ENSG00000274020 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1444399089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23121276 77165 RMVar_ID_77165 Human_SNP_ID_32974987 m1A Human chr1 - 148522660 148522660 148522660 CAGAGGTCAGCACATCTGGAACGCAATGGATAAGCCGCGACCATGAGAAAAGCGCCTTCATGATC CAGAGGTCAGCACATCTGGAACGCAATGGATACGCCGCGACCATGAGAAAAGCGCCTTCATGATC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:148522601..148522675 26863196 MeRIP-seq:(Medium) rs1382998901 Functional Loss SNV dbSNP153 33..33 33 - - - 77166 RMVar_ID_77166 Human_SNP_ID_32974998 m1A Human chr1 + 148522666 148522666 148522666 GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCATTGCGTTCCAGATGTGCTGACCTCTGCGATTT GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCCTTGCGTTCCAGATGTGCTGACCTCTGCGATTT A C RNVU1-27 Ensembl:ENSG00000274210 snRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:148522601..148522750 26863196 MeRIP-seq:(Medium) rs1192439688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800737,Human_RBP_ID_1438979,Human_RBP_ID_1724708,Human_RBP_ID_2092181,Human_RBP_ID_5253989,Human_RBP_ID_8171179,Human_RBP_ID_8955497,Human_RBP_ID_9455487,Human_RBP_ID_10564040,Human_RBP_ID_17066651,Human_RBP_ID_17072900,Human_RBP_ID_17180773,Human_RBP_ID_17667605,Human_RBP_ID_17674908,Human_RBP_ID_17762845,Human_RBP_ID_18198321,Human_RBP_ID_18205224,Human_RBP_ID_18415047,Human_RBP_ID_18509888,Human_RBP_ID_18550575,Human_RBP_ID_19444789,Human_RBP_ID_21913510,Human_RBP_ID_22015540,Human_RBP_ID_22779667,Human_RBP_ID_22846371,Human_RBP_ID_23110089,Human_RBP_ID_23263638,Human_RBP_ID_23329922,Human_RBP_ID_24395306,Human_RBP_ID_26747257,Human_RBP_ID_26840581 77167 RMVar_ID_77167 Human_SNP_ID_32974999 m1A Human chr1 + 148522666 148522666 148522666 GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCATTGCGTTCCAGATGTGCTGACCTCTGCGATTT GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCGTTGCGTTCCAGATGTGCTGACCTCTGCGATTT A G RNVU1-27 Ensembl:ENSG00000274210 snRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:148522601..148522750 26863196 MeRIP-seq:(Medium) rs1192439688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800737,Human_RBP_ID_1438979,Human_RBP_ID_1724708,Human_RBP_ID_2092181,Human_RBP_ID_5253989,Human_RBP_ID_8171179,Human_RBP_ID_8955497,Human_RBP_ID_9455487,Human_RBP_ID_10564040,Human_RBP_ID_17066651,Human_RBP_ID_17072900,Human_RBP_ID_17180773,Human_RBP_ID_17667605,Human_RBP_ID_17674908,Human_RBP_ID_17762845,Human_RBP_ID_18198321,Human_RBP_ID_18205224,Human_RBP_ID_18415047,Human_RBP_ID_18509888,Human_RBP_ID_18550575,Human_RBP_ID_19444789,Human_RBP_ID_21913510,Human_RBP_ID_22015540,Human_RBP_ID_22779667,Human_RBP_ID_22846371,Human_RBP_ID_23110089,Human_RBP_ID_23263638,Human_RBP_ID_23329922,Human_RBP_ID_24395306,Human_RBP_ID_26747257,Human_RBP_ID_26840581 77168 RMVar_ID_77168 Human_SNP_ID_32975000 m1A Human chr1 + 148522666 148522666 148522666 GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCATTGCGTTCCAGATGTGCTGACCTCTGCGATTT GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCTTTGCGTTCCAGATGTGCTGACCTCTGCGATTT A T RNVU1-27 Ensembl:ENSG00000274210 snRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:148522601..148522750 26863196 MeRIP-seq:(Medium) rs1192439688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800737,Human_RBP_ID_1438979,Human_RBP_ID_1724708,Human_RBP_ID_2092181,Human_RBP_ID_5253989,Human_RBP_ID_8171179,Human_RBP_ID_8955497,Human_RBP_ID_9455487,Human_RBP_ID_10564040,Human_RBP_ID_17066651,Human_RBP_ID_17072900,Human_RBP_ID_17180773,Human_RBP_ID_17667605,Human_RBP_ID_17674908,Human_RBP_ID_17762845,Human_RBP_ID_18198321,Human_RBP_ID_18205224,Human_RBP_ID_18415047,Human_RBP_ID_18509888,Human_RBP_ID_18550575,Human_RBP_ID_19444789,Human_RBP_ID_21913510,Human_RBP_ID_22015540,Human_RBP_ID_22779667,Human_RBP_ID_22846371,Human_RBP_ID_23110089,Human_RBP_ID_23263638,Human_RBP_ID_23329922,Human_RBP_ID_24395306,Human_RBP_ID_26747257,Human_RBP_ID_26840581 77169 RMVar_ID_77169 Human_SNP_ID_32975070 m1A Human chr1 - 148522708 148522708 148522708 CCACTATCACAAATTATGCAGTCGAGTTTCCCACATTTGGGGAAATCGCAGAGGTCAGCACATCT CCACTATCACAAATTATGCAGTCGAGTTTCCCTCATTTGGGGAAATCGCAGAGGTCAGCACATCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:148522659..148522736 26863196 MeRIP-seq:(Medium) rs1446871818 Functional Loss SNV dbSNP153 33..33 33 - - - 77170 RMVar_ID_77170 Human_SNP_ID_32975071 m1A Human chr1 - 148522708 148522708 148522708 CCACTATCACAAATTATGCAGTCGAGTTTCCCACATTTGGGGAAATCGCAGAGGTCAGCACATCT CCACTATCACAAATTATGCAGTCGAGTTTCCCCCATTTGGGGAAATCGCAGAGGTCAGCACATCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:148522659..148522736 26863196 MeRIP-seq:(Medium) rs1446871818 Functional Loss SNV dbSNP153 33..33 33 - - - 77171 RMVar_ID_77171 Human_SNP_ID_32975092 m1A Human chr1 - 148522721 148522721 148522721 CGAACGCAGCCCCCCACTATCACAAATTATGCAGTCGAGTTTCCCACATTTGGGGAAATCGCAGA CGAACGCAGCCCCCCACTATCACAAATTATGCTGTCGAGTTTCCCACATTTGGGGAAATCGCAGA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:148522601..148522775 26863196 MeRIP-seq:(Medium) rs1244016848 Functional Loss SNV dbSNP153 33..33 33 - - - 77172 RMVar_ID_77172 Human_SNP_ID_32980045 m1A Human chr1 - 148532727 148532727 148532727 TTTTAATTTGAACCACGTATCTCTGGGTAGCTACAAAATTCCTCAGGGATTTCATTTTGCAGGCA TTTTAATTTGAACCACGTATCTCTGGGTAGCTGCAAAATTCCTCAGGGATTTCATTTTGCAGGCA T C NBPF14 Ensembl:ENSG00000270629 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1329712810 Functional Loss SNV dbSNP153 33..33 33 - - - 77173 RMVar_ID_77173 Human_SNP_ID_33004253 m1A Human chr1 - 148679551 148679551 148679551 CCCATGTGGATCTGCCCAGGCGGCGGCGGCGGAGGAGGCGACCGAGAAGATGCCCGCCCTGCGCC CCCATGTGGATCTGCCCAGGCGGCGGCGGCGGCGGAGGCGACCGAGAAGATGCCCGCCCTGCGCC T G NBPF14,NOTCH2NLB Ensembl:ENSG00000270629,Ensembl:ENSG00000286019 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:148679476..148679600 26863196 MeRIP-seq:(Medium) rs1427315297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_123223,Human_Splice_Rec_123237 77174 RMVar_ID_77174 Human_SNP_ID_33004281 m1A Human chr1 - 148679703 148679703 148679703 GGGCGGCTGAGGCGGCGGCCGAGGAGCGGCGGACTCCGGGCGCGGGGAGTCGAGGCATTTGCGCC GGGCGGCTGAGGCGGCGGCCGAGGAGCGGCGGTCTCCGGGCGCGGGGAGTCGAGGCATTTGCGCC T A NBPF14,NOTCH2NLB Ensembl:ENSG00000270629,Ensembl:ENSG00000286019 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:148679607..148679720 26863196 MeRIP-seq:(Medium) rs1447026524 Functional Loss SNV dbSNP153 33..33 33 - - - 77175 RMVar_ID_77175 Human_SNP_ID_33056515 m1A Human chr1 - 148952149 148952149 148952149 AGCCGCTTTCATCTGCTAAGACCTCACCTGAAAGTCGCACCAGTGCCCTCAAGGATCCTCCCGCC AGCCGCTTTCATCTGCTAAGACCTCACCTGAAGGTCGCACCAGTGCCCTCAAGGATCCTCCCGCC T C piR-30644,lnc-NBPF9-8,lnc-NBPF9-8:2 RNACentral:URS00002E6C3A,RNACentral:URS0000D5B26E,RNACentral:URS0000D5C0F7 piRNA,lincRNA,lincRNA intron,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:148952065..148952148;chr1:148952075..148952213 26863196 MeRIP-seq:(Medium) rs1366064644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5540052,Human_RBP_ID_5642583,Human_RBP_ID_18524101 77176 RMVar_ID_77176 Human_SNP_ID_33058399 m1A Human chr1 + 148956140 148956140 148956140 CTCTGAACAAATATGGAAAGAATAGAAATAATATAATTTTTTTTGGTAGTTCTCTTTTTTAGTTT CTCTGAACAAATATGGAAAGAATAGAAATAATGTAATTTTTTTTGGTAGTTCTCTTTTTTAGTTT A G PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2762864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24580998 RMVar_hsa_circ_304527,RMVar_hsa_circ_49122 77177 RMVar_ID_77177 Human_SNP_ID_33091794 m1A Human chr1 - 149054720 149054719 149054720 ATAATGTAGCTGCATTTCTTTAGTTATTTTGAACCCCAAATATTTCCTCATCTTTTTGTTGTTGT ATAATGTAGCTGCATTTCTTTAGTTATTTTGA_CCCCAAATATTTCCTCATCTTTTTGTTGTTGT GT G NBPF9 Ensembl:ENSG00000269713 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1322421855 Functional Loss DEL dbSNP153 33..33 33 - - - 77178 RMVar_ID_77178 Human_SNP_ID_33092155 m1A Human chr1 - 149055530 149055530 149055530 CAGACATAGGATGGGTCAGTGGGCATGGCTCTATTCCTATTCTCAAACCATGCCAGTGGCAACCT CAGACATAGGATGGGTCAGTGGGCATGGCTCTTTTCCTATTCTCAAACCATGCCAGTGGCAACCT T A NBPF9 Ensembl:ENSG00000269713 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12124435 Functional Loss SNV dbSNP153 33..33 33 - - - 77179 RMVar_ID_77179 Human_SNP_ID_33092156 m1A Human chr1 - 149055530 149055530 149055530 CAGACATAGGATGGGTCAGTGGGCATGGCTCTATTCCTATTCTCAAACCATGCCAGTGGCAACCT CAGACATAGGATGGGTCAGTGGGCATGGCTCTGTTCCTATTCTCAAACCATGCCAGTGGCAACCT T C NBPF9 Ensembl:ENSG00000269713 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12124435 Functional Loss SNV dbSNP153 33..33 33 - - - 77180 RMVar_ID_77180 Human_SNP_ID_33092286 m1A Human chr1 - 149055656 149055656 149055656 GTGTTCCAGATGGAAGTCATATTCCCACAATAAGCAGCCCTTACTAAGCCGAGAGATGTCATTCC GTGTTCCAGATGGAAGTCATATTCCCACAATATGCAGCCCTTACTAAGCCGAGAGATGTCATTCC T A NBPF9 Ensembl:ENSG00000269713 Protein coding stop codon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78667364 Functional Loss SNV dbSNP153 33..33 33 - - - 77181 RMVar_ID_77181 Human_SNP_ID_33092287 m1A Human chr1 - 149055656 149055656 149055656 GTGTTCCAGATGGAAGTCATATTCCCACAATAAGCAGCCCTTACTAAGCCGAGAGATGTCATTCC GTGTTCCAGATGGAAGTCATATTCCCACAATAGGCAGCCCTTACTAAGCCGAGAGATGTCATTCC T C NBPF9 Ensembl:ENSG00000269713 Protein coding stop codon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78667364 Functional Loss SNV dbSNP153 33..33 33 - - - 77182 RMVar_ID_77182 Human_SNP_ID_33098960 m1A Human chr1 - 149070991 149070991 149070991 AAATCACATTTGAGGAAGACAAAGTCGACTCAACTCTCATTGGCTCATCCTCTCATGTTGAACGG AAATCACATTTGAGGAAGACAAAGTCGACTCAGCTCTCATTGGCTCATCCTCTCATGTTGAACGG T C NBPF9 Ensembl:ENSG00000269713 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs797023053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2091205 Human_Splice_Rec_124161,Human_Splice_Rec_124209,Human_Splice_Rec_124257,Human_Splice_Rec_124297,Human_Splice_Rec_124331,Human_Splice_Rec_124413,Human_Splice_Rec_124451 RMVar_hsa_circ_12213,RMVar_hsa_circ_60860 77183 RMVar_ID_77183 Human_SNP_ID_33164424 m1A Human chr1 - 149390703 149390703 149390703 TCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAAGCACAGGCGCAAATGCCTCGACTCCCCGCGCC TCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAGGCACAGGCGCAAATGCCTCGACTCCCCGCGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:149390620..149390868;chr1:149390619..149390782 26863196 MeRIP-seq:(Medium) rs1384983615 Functional Loss SNV dbSNP153 33..33 33 - - - 77184 RMVar_ID_77184 Human_SNP_ID_33164425 m1A Human chr1 - 149390703 149390703 149390703 TCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAAGCACAGGCGCAAATGCCTCGACTCCCCGCGCC TCAAAGGCTCAGGCCCTGGCGCTACGGTCCGACGCACAGGCGCAAATGCCTCGACTCCCCGCGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:149390620..149390868;chr1:149390619..149390782 26863196 MeRIP-seq:(Medium) rs1384983615 Functional Loss SNV dbSNP153 33..33 33 - - - 77185 RMVar_ID_77185 Human_SNP_ID_33164426 m1A Human chr1 - 149390704 149390704 149390704 TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAAGCACAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGTAGCACAGGCGCAAATGCCTCGACTCCCCGCGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:149390654..149390919 26863196 MeRIP-seq:(Medium) rs1415523463 Functional Loss SNV dbSNP153 33..33 33 - - - 77186 RMVar_ID_77186 Human_SNP_ID_33164427 m1A Human chr1 - 149390704 149390704 149390704 TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAAGCACAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGGAGCACAGGCGCAAATGCCTCGACTCCCCGCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:149390654..149390919 26863196 MeRIP-seq:(Medium) rs1415523463 Functional Loss SNV dbSNP153 33..33 33 - - - 77187 RMVar_ID_77187 Human_SNP_ID_33164428 m1A Human chr1 - 149390704 149390704 149390704 TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGAAGCACAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGGTCCGCAGCACAGGCGCAAATGCCTCGACTCCCCGCGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:149390654..149390919 26863196 MeRIP-seq:(Medium) rs1415523463 Functional Loss SNV dbSNP153 33..33 33 - - - 77188 RMVar_ID_77188 Human_SNP_ID_33164435 m1A Human chr1 + 149390708 149390708 149390708 GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGACCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGCCCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG A C AC242842.3,NOTCH2NLC Ensembl:ENSG00000286185,Ensembl:ENSG00000286219 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149390655..149390908 26863196 MeRIP-seq:(Medium) rs1313747809 Functional Loss SNV dbSNP153 33..33 33 - - - 77189 RMVar_ID_77189 Human_SNP_ID_33164436 m1A Human chr1 + 149390708 149390708 149390708 GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGACCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGGCCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG A G AC242842.3,NOTCH2NLC Ensembl:ENSG00000286185,Ensembl:ENSG00000286219 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149390655..149390908 26863196 MeRIP-seq:(Medium) rs1313747809 Functional Loss SNV dbSNP153 33..33 33 - - - 77190 RMVar_ID_77190 Human_SNP_ID_33164437 m1A Human chr1 + 149390708 149390708 149390708 GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGACCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG GGGGAGTCGAGGCATTTGCGCCTGTGCTTCGGTCCGTAGCGCCAGGGCCTGAGCCTTTGAAGCAG A T AC242842.3,NOTCH2NLC Ensembl:ENSG00000286185,Ensembl:ENSG00000286219 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149390655..149390908 26863196 MeRIP-seq:(Medium) rs1313747809 Functional Loss SNV dbSNP153 33..33 33 - - - 77191 RMVar_ID_77191 Human_SNP_ID_33201252 m1A Human chr1 + 149607337 149607337 149607337 TCCTCCTCCTCCTCTCACCCAGGATCACTTCCAAAACCACTTGGCCTTCAGCCCCTGCCTCGGCC TCCTCCTCCTCCTCTCACCCAGGATCACTTCCGAAACCACTTGGCCTTCAGCCCCTGCCTCGGCC A G LINC00869 Ensembl:ENSG00000277147 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149607295..149607387 26863196 MeRIP-seq:(Medium) rs7512396 Functional Loss SNV dbSNP153 33..33 33 - - - 77192 RMVar_ID_77192 Human_SNP_ID_33212372 m1A Human chr1 - 149646728 149646728 149646728 CCAGGCGTCTCGGGCTGGGTCGCCGACCGGGGAGTTTCTGGGGTCTCTCCCTCTGGCTCCAGAAT CCAGGCGTCTCGGGCTGGGTCGCCGACCGGGGCGTTTCTGGGGTCTCTCCCTCTGGCTCCAGAAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149646575..149646754 26863196 MeRIP-seq:(Medium) rs1553725126 Functional Loss SNV dbSNP153 33..33 33 - - - 77193 RMVar_ID_77193 Human_SNP_ID_33257332 m1A Human chr1 - 149813518 149813518 149813518 CGGCACCGTGGCTCTGCGGGAGATCCGGCGCTACCAGAAGTCTACGGAGCTGCTGATCCGCAAGC CGGCACCGTGGCTCTGCGGGAGATCCGGCGCTGCCAGAAGTCTACGGAGCTGCTGATCCGCAAGC T C H3C13 Ensembl:ENSG00000183598 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:149813476..149813575;chr1:149813501..149813550;chr1:149813493..149813585;chr1:149813501..149813575 26863196 MeRIP-seq:(Medium) rs1553754941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4080618,Human_RBP_ID_22427466,Human_RBP_ID_22749410 77194 RMVar_ID_77194 Human_SNP_ID_33267039 m1A Human chr1 + 149886407 149886407 149886407 GTGGAGCGCTTGTTGTAGTGCGCCAGGCGGGAAGCCTCTCCCGCGATGCGCTCGAAGATGTCGTT GTGGAGCGCTTGTTGTAGTGCGCCAGGCGGGACGCCTCTCCCGCGATGCGCTCGAAGATGTCGTT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:149886309..149886675 26863196 MeRIP-seq:(Medium) rs587664229 Functional Loss SNV dbSNP153 33..33 33 - - - 77195 RMVar_ID_77195 Human_SNP_ID_33267040 m1A Human chr1 - 149886413 149886413 149886413 TTCGTCAACGACATCTTCGAGCGCATCGCGGGAGAGGCTTCCCGCCTGGCGCACTACAACAAGCG TTCGTCAACGACATCTTCGAGCGCATCGCGGGTGAGGCTTCCCGCCTGGCGCACTACAACAAGCG T A H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149886363..149886437 26863196 MeRIP-seq:(Medium) rs781785808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224664,Human_RBP_ID_325106,Human_RBP_ID_1149338,Human_RBP_ID_1411066,Human_RBP_ID_8955590,Human_RBP_ID_17679064,Human_RBP_ID_17724650,Human_RBP_ID_18187244,Human_RBP_ID_22429637,Human_RBP_ID_26798797 77196 RMVar_ID_77196 Human_SNP_ID_33267089 m1A Human chr1 - 149886536 149886536 149886536 AAAGACGGCAAGAAGCGCAAGCGCAGCCGCAAAGAGAGCTACTCCATCTACGTGTACAAGGTGCT AAAGACGGCAAGAAGCGCAAGCGCAGCCGCAAGGAGAGCTACTCCATCTACGTGTACAAGGTGCT T C H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr1:149886273..149886675;chr1:149886302..149886675 26863196 MeRIP-seq:(Medium) rs782404356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325107,Human_RBP_ID_745707,Human_RBP_ID_970826,Human_RBP_ID_1411068,Human_RBP_ID_1724777,Human_RBP_ID_3280336,Human_RBP_ID_5685322,Human_RBP_ID_9319114,Human_RBP_ID_17445787,Human_RBP_ID_18522557,Human_RBP_ID_18550706,Human_RBP_ID_22430884,Human_RBP_ID_26314617,Human_RBP_ID_26798801,Human_RBP_ID_26840691 77197 RMVar_ID_77197 Human_SNP_ID_33267090 m1A Human chr1 - 149886537 149886537 149886537 GAAAGACGGCAAGAAGCGCAAGCGCAGCCGCAAAGAGAGCTACTCCATCTACGTGTACAAGGTGC GAAAGACGGCAAGAAGCGCAAGCGCAGCCGCAGAGAGAGCTACTCCATCTACGTGTACAAGGTGC T C H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:149886501..149886675 26863196 MeRIP-seq:(Medium) rs1553759756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745707,Human_RBP_ID_970826,Human_RBP_ID_1411068,Human_RBP_ID_1724777,Human_RBP_ID_5685322,Human_RBP_ID_9319114,Human_RBP_ID_17445787,Human_RBP_ID_18522557,Human_RBP_ID_18550707,Human_RBP_ID_22430884,Human_RBP_ID_26314617,Human_RBP_ID_26798801,Human_RBP_ID_26840691 77198 RMVar_ID_77198 Human_SNP_ID_33267136 m1A Human chr1 - 149886623 149886623 149886623 GTACTGTGTCTTACCATGCCTGAACCGGCAAAATCCGCTCCGGCCCCTAAAAAGGGCTCCAAGAA GTACTGTGTCTTACCATGCCTGAACCGGCAAAGTCCGCTCCGGCCCCTAAAAAGGGCTCCAAGAA T C H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr1:149886399..149886675;chr1:149886525..149886675 26863196 MeRIP-seq:(Medium) rs1553759778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224665,Human_RBP_ID_745708,Human_RBP_ID_970828,Human_RBP_ID_1411071,Human_RBP_ID_1724778,Human_RBP_ID_3280338,Human_RBP_ID_4075900,Human_RBP_ID_5278528,Human_RBP_ID_5484243,Human_RBP_ID_5519918,Human_RBP_ID_8284342,Human_RBP_ID_8955591,Human_RBP_ID_9319115,Human_RBP_ID_17212056,Human_RBP_ID_17445788,Human_RBP_ID_17724651,Human_RBP_ID_18550709,Human_RBP_ID_19186273,Human_RBP_ID_22427468,Human_RBP_ID_22485781,Human_RBP_ID_22779751,Human_RBP_ID_23205311,Human_RBP_ID_26367636,Human_RBP_ID_26798805 77199 RMVar_ID_77199 Human_SNP_ID_33267411 m1A Human chr1 + 149887126 149887126 149887126 CGCGGAGCGGGTGGGGGCCGGCGCGCCCGTCTACATGGCGGCGGTCCTCGAGTACCTGACCGCCG CGCGGAGCGGGTGGGGGCCGGCGCGCCCGTCTGCATGGCGGCGGTCCTCGAGTACCTGACCGCCG A G H2AC20 Ensembl:ENSG00000184260 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:149887101..149887125 26863196 MeRIP-seq:(Medium) rs1553759892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224656,Human_RBP_ID_325116,Human_RBP_ID_970834,Human_RBP_ID_4080645,Human_RBP_ID_17724654,Human_RBP_ID_18428476,Human_RBP_ID_22428565,Human_RBP_ID_22779755,Human_RBP_ID_26389712,Human_RBP_ID_26840698,Human_RBP_ID_27167322 77200 RMVar_ID_77200 Human_SNP_ID_33276987 m1A Human chr1 - 149923517 149923517 149923517 CTCAGTAAATTCACATTTTCCTTCCTCCTGTTACATTTTCCCAATATCTTTTCTATTCCTTGGAC CTCAGTAAATTCACATTTTCCTTCCTCCTGTTTCATTTTCCCAATATCTTTTCTATTCCTTGGAC T A SF3B4 Ensembl:ENSG00000143368 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:149923466..149923716 32194978 MeRIP-seq:(Medium) rs900173937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325153,Human_RBP_ID_970851,Human_RBP_ID_1344629,Human_RBP_ID_1724802,Human_RBP_ID_2092399,Human_RBP_ID_5137619,Human_RBP_ID_5685371,Human_RBP_ID_8043380,Human_RBP_ID_8955615,Human_RBP_ID_10565470,Human_RBP_ID_16969874,Human_RBP_ID_17212073,Human_RBP_ID_17329989,Human_RBP_ID_17445798,Human_RBP_ID_17647046,Human_RBP_ID_17724684,Human_RBP_ID_18929925,Human_RBP_ID_22420256,Human_RBP_ID_23260281,Human_RBP_ID_24395321,Human_RBP_ID_26367662 Human_miRNA_ID_479000,Human_miRNA_ID_1162832,Human_miRNA_ID_1167628,Human_miRNA_ID_1216850 77201 RMVar_ID_77201 Human_SNP_ID_33276999 m1A Human chr1 + 149923564 149923558 149923565 AAATGTGAATTTACTGAGGGAGAGGGCCTCGAAGTGGGCCTCGAGGGGGAACTGGTGGCCGGGGA AAATGTGAATTTACTGAGGGAGAGGGC_______TGGGCCTCGAGGGGGAACTGGTGGCCGGGGA CCTCGAAG C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:149923466..149923566 26863410 MeRIP-seq:(Medium) rs797045121 Functional Loss DEL dbSNP153 28..34 33 - - - Clinvar_Rec_355 77202 RMVar_ID_77202 Human_SNP_ID_33277024 m1A Human chr1 + 149923615 149923615 149923615 CTGGTGGCCGGGGAGTGGGTCTGGGTGGAGGGAGAGGCCCCCGCTGGTAGCCATAGGGTGGGGGT CTGGTGGCCGGGGAGTGGGTCTGGGTGGAGGGTGAGGCCCCCGCTGGTAGCCATAGGGTGGGGGT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:149923500..149923750 26863196 MeRIP-seq:(Medium) rs962899023 Functional Loss SNV dbSNP153 33..33 33 - - - 77203 RMVar_ID_77203 Human_SNP_ID_33277718 m1A Human chr1 - 149926005 149926005 149926005 CCTCCTCCTGGCTCCTTCCCACCCCCAGTGCCACCTCCTGGAGCCCTCCCACCTGGGATACCCCC CCTCCTCCTGGCTCCTTCCCACCCCCAGTGCCGCCTCCTGGAGCCCTCCCACCTGGGATACCCCC T C SF3B4 Ensembl:ENSG00000143368 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149925955..149926034 26863196 MeRIP-seq:(Medium) rs200149254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224074,Human_RBP_ID_325166,Human_RBP_ID_746634,Human_RBP_ID_17338384,Human_RBP_ID_18929927,Human_RBP_ID_24746894,Human_RBP_ID_26840745,Human_RBP_ID_27167369,Human_RBP_ID_27387546 Human_Splice_Rec_125314 RMVar_hsa_circ_48526 77204 RMVar_ID_77204 Human_SNP_ID_33277828 m1A Human chr1 + 149926425 149926425 149926425 GACCCCAATGATGATACCACAGGATTGGGAGCAGAGGGTGGAGGAGGTGCATCTGCAAACAGCTG GACCCCAATGATGATACCACAGGATTGGGAGCGGAGGGTGGAGGAGGTGCATCTGCAAACAGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149926379..149926558 26863196 MeRIP-seq:(Medium) rs782141723 Functional Loss SNV dbSNP153 33..33 33 - - - 77205 RMVar_ID_77205 Human_SNP_ID_33277836 m1A Human chr1 + 149926470 149926470 149926470 GGTGCATCTGCAAACAGCTGATGAGGGCGATCAGCCTGGGAGAGCGGGTTCTGAGCTGCCAGAAG GGTGCATCTGCAAACAGCTGATGAGGGCGATCCGCCTGGGAGAGCGGGTTCTGAGCTGCCAGAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149926420..149926489 26863196 MeRIP-seq:(Medium) rs587684161 Functional Loss SNV dbSNP153 33..33 33 - - - 77206 RMVar_ID_77206 Human_SNP_ID_33277837 m1A Human chr1 + 149926470 149926470 149926470 GGTGCATCTGCAAACAGCTGATGAGGGCGATCAGCCTGGGAGAGCGGGTTCTGAGCTGCCAGAAG GGTGCATCTGCAAACAGCTGATGAGGGCGATCGGCCTGGGAGAGCGGGTTCTGAGCTGCCAGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149926420..149926489 26863196 MeRIP-seq:(Medium) rs587684161 Functional Loss SNV dbSNP153 33..33 33 - - - 77207 RMVar_ID_77207 Human_SNP_ID_33278185 m1A Human chr1 - 149927759 149927759 149927759 CGCTGCTGGGAGACGGCGGGATCTCTTTCGCCATGGCTGCCGGGCCGATCTCCGAGCGGAATCAG CGCTGCTGGGAGACGGCGGGATCTCTTTCGCCGTGGCTGCCGGGCCGATCTCCGAGCGGAATCAG T C SF3B4 Ensembl:ENSG00000143368 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:149927694..149927800;chr1:149927726..149927800 26863196 MeRIP-seq:(Medium) rs387907185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1411130,Human_RBP_ID_4074348,Human_RBP_ID_5484262,Human_RBP_ID_8734429,Human_RBP_ID_9319118,Human_RBP_ID_22871832,Human_RBP_ID_26311727 Human_Splice_Rec_125309 Clinvar_Rec_356 RMVar_hsa_circ_135861,RMVar_hsa_circ_107192 77208 RMVar_ID_77208 Human_SNP_ID_33278200 m1A Human chr1 - 149927771 149927771 149927771 AGAAGGCGGAACCGCTGCTGGGAGACGGCGGGATCTCTTTCGCCATGGCTGCCGGGCCGATCTCC AGAAGGCGGAACCGCTGCTGGGAGACGGCGGGGTCTCTTTCGCCATGGCTGCCGGGCCGATCTCC T C SF3B4 Ensembl:ENSG00000143368 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:149927661..149927800 26863196 MeRIP-seq:(Medium) rs369314933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074348,Human_RBP_ID_5484262,Human_RBP_ID_8734429,Human_RBP_ID_17724707,Human_RBP_ID_22485787,Human_RBP_ID_22871832 Human_Splice_Rec_125309 RMVar_hsa_circ_135861,RMVar_hsa_circ_107192 77209 RMVar_ID_77209 Human_SNP_ID_33281068 m1A Human chr1 + 149936783 149936783 149936783 GGGAGAGGGGTAGGGGGTTGGACACAAGGGAAAGGAGCATTTGACGTGCACGGAGCAGAGTTTGG GGGAGAGGGGTAGGGGGTTGGACACAAGGGAAGGGAGCATTTGACGTGCACGGAGCAGAGTTTGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:149936681..149936851 26863196 MeRIP-seq:(Medium) rs1224033642 Functional Loss SNV dbSNP153 33..33 33 - - - 77210 RMVar_ID_77210 Human_SNP_ID_33282685 m1A Human chr1 - 149943709 149943709 149943709 TGGCTGGAAACTTTTAAGTGTGTGCACACAGGAGTGCTGCCAGGCTGGCAAGAGCAGGTCGGGGC TGGCTGGAAACTTTTAAGTGTGTGCACACAGGCGTGCTGCCAGGCTGGCAAGAGCAGGTCGGGGC T G OTUD7B Ensembl:ENSG00000264522 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:149943599..149943793 26863196 MeRIP-seq:(Medium) rs1031818696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5685543 Human_miRNA_ID_1387290 77211 RMVar_ID_77211 Human_SNP_ID_33283075 m1A Human chr1 - 149944743 149944743 149944743 GTTGGGAGGAAGCAGCGGCACTGAGACACTGGAGAAGAAGAAGAAAAACTCACTGAAGAGCTGGA GTTGGGAGGAAGCAGCGGCACTGAGACACTGGGGAAGAAGAAGAAAAACTCACTGAAGAGCTGGA T C OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:149944355..149945048 26863196 MeRIP-seq:(Medium) rs1559821559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850343,Human_RBP_ID_3936513,Human_RBP_ID_10565817,Human_RBP_ID_24541830 Human_miRNA_ID_1538152,Human_miRNA_ID_1592574 77212 RMVar_ID_77212 Human_SNP_ID_33283145 m1A Human chr1 - 149944936 149944936 149944936 GCAGTTCCACCAGCAACGAGGGCGGCCGGCGGAAGGAGAAGTCAAAGCGAGATCGGGAGAAGGAC GCAGTTCCACCAGCAACGAGGGCGGCCGGCGGTAGGAGAAGTCAAAGCGAGATCGGGAGAAGGAC T A OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:149944897..149944998 32194978 MeRIP-seq:(Medium) rs1204845662 Functional Loss SNV dbSNP153 33..33 33 - - - 77213 RMVar_ID_77213 Human_SNP_ID_33288370 m1A Human chr1 - 149965880 149965880 149965880 AATCTCCTTTTCCTCCACTATCTTGTTTCTACAGGGCGTTTGAACTGGTGGGTGAGTGTGGATCC AATCTCCTTTTCCTCCACTATCTTGTTTCTACGGGGCGTTTGAACTGGTGGGTGAGTGTGGATCC T C OTUD7B Ensembl:ENSG00000264522 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:149965836..149967451 32194978 MeRIP-seq:(Medium) rs1327992272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135866,RMVar_hsa_circ_335443,RMVar_hsa_circ_359311,RMVar_hsa_circ_289132,RMVar_hsa_circ_337125,RMVar_hsa_circ_102415,RMVar_hsa_circ_308460,RMVar_hsa_circ_346535,RMVar_hsa_circ_276934 77214 RMVar_ID_77214 Human_SNP_ID_33288680 m1A Human chr1 - 149967425 149967425 149967425 TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCAATGAGCACCCCCTGGAAATGCCCATCTGTGCCT TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCATTGAGCACCCCCTGGAAATGCCCATCTGTGCCT T A OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149967376..149967458 26863196 MeRIP-seq:(Medium) rs1553776847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223296 Human_Splice_Rec_125498,Human_Splice_Rec_125520 RMVar_hsa_circ_135866,RMVar_hsa_circ_335443,RMVar_hsa_circ_359311,RMVar_hsa_circ_289132,RMVar_hsa_circ_337125,RMVar_hsa_circ_102415,RMVar_hsa_circ_44952,RMVar_hsa_circ_308460,RMVar_hsa_circ_346535,RMVar_hsa_circ_276934 77215 RMVar_ID_77215 Human_SNP_ID_33288681 m1A Human chr1 - 149967425 149967425 149967425 TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCAATGAGCACCCCCTGGAAATGCCCATCTGTGCCT TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCAGTGAGCACCCCCTGGAAATGCCCATCTGTGCCT T C OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149967376..149967458 26863196 MeRIP-seq:(Medium) rs1553776847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223296 Human_Splice_Rec_125498,Human_Splice_Rec_125520 RMVar_hsa_circ_135866,RMVar_hsa_circ_335443,RMVar_hsa_circ_359311,RMVar_hsa_circ_289132,RMVar_hsa_circ_337125,RMVar_hsa_circ_102415,RMVar_hsa_circ_44952,RMVar_hsa_circ_308460,RMVar_hsa_circ_346535,RMVar_hsa_circ_276934 77216 RMVar_ID_77216 Human_SNP_ID_33290931 m1A Human chr1 + 149977575 149977575 149977575 TAGGTAGAACATAGATCAAAATTCAGGCCTCCACCTGAGGAATAAATAAATACATAAGGCTCAAA TAGGTAGAACATAGATCAAAATTCAGGCCTCCCCCTGAGGAATAAATAAATACATAAGGCTCAAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:149971241..150010626 32194978 MeRIP-seq:(Medium) rs901002902 Functional Loss SNV dbSNP153 33..33 33 - - - 77217 RMVar_ID_77217 Human_SNP_ID_233854007 m1A Human chr5 - 60700017 60700001 60700018 GCTGGTGAGTGAGTGTGCTGGGGCCTGGGCGGAGCACCCGGTGCCGCGAGCCCCCACTCAGCGCG GCTGGTGAGTGAGTGTGCTGGGGCCTGGGCG_________________AGCCCCCACTCAGCGCG TCGCGGCACCGGGTGCTC T DEPDC1B Ensembl:ENSG00000035499 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:60700015..60700123 26863196 MeRIP-seq:(Medium) rs1181910737 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_944264,Human_RBP_ID_24110259 77218 RMVar_ID_77218 Human_SNP_ID_233854018 m1A Human chr5 - 60700017 60700017 60700017 GCTGGTGAGTGAGTGTGCTGGGGCCTGGGCGGAGCACCCGGTGCCGCGAGCCCCCACTCAGCGCG GCTGGTGAGTGAGTGTGCTGGGGCCTGGGCGGGGCACCCGGTGCCGCGAGCCCCCACTCAGCGCG T C DEPDC1B Ensembl:ENSG00000035499 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:60700015..60700123 26863196 MeRIP-seq:(Medium) rs1442477476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944264,Human_RBP_ID_24110259 77219 RMVar_ID_77219 Human_SNP_ID_233854076 m1A Human chr5 + 60700105 60700105 60700105 CCCCACGATGCGATGCTCCATGGCGCGTAGGCAGCAGCGGCCGCAGCCGCGCCAGCGCTGATCCC CCCCACGATGCGATGCTCCATGGCGCGTAGGCCGCAGCGGCCGCAGCCGCGCCAGCGCTGATCCC A C AC109133.1 Ensembl:ENSG00000287434 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:60700006..60700105 26863196 MeRIP-seq:(Medium) rs1197402649 Functional Loss SNV dbSNP153 33..33 33 - - - 77220 RMVar_ID_77220 Human_SNP_ID_233912948 m1A Human chr5 + 60945232 60945232 60945232 GCATTACCCCTACTGCGGGTCCCGCTGCTGGCAGCGCTGGAAACTGGGTGGACGGCATGGGTTGG GCATTACCCCTACTGCGGGTCCCGCTGCTGGCGGCGCTGGAAACTGGGTGGACGGCATGGGTTGG A G NDUFAF2 Ensembl:ENSG00000164182 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:60945176..60945399;chr5:60945176..60945425;chr5:60945176..61050415 26863196 MeRIP-seq:(Medium) rs753884526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942810,Human_RBP_ID_4834891,Human_RBP_ID_17415195,Human_RBP_ID_26352122,Human_RBP_ID_27826385 77221 RMVar_ID_77221 Human_SNP_ID_233913038 m1A Human chr5 + 60945386 60945386 60945386 CTACATCCCGCAGTACAAGAACTGGAGAGGTGAGGTGGCGGCGTGGGCAGCGATTGCGTGGTCAG CTACATCCCGCAGTACAAGAACTGGAGAGGTGGGGTGGCGGCGTGGGCAGCGATTGCGTGGTCAG A G NDUFAF2 Ensembl:ENSG00000164182 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:60945370..61050415 32194978 MeRIP-seq:(Medium) rs1458719743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5427404,Human_RBP_ID_7452674 Human_Splice_Rec_654441 77222 RMVar_ID_77222 Human_SNP_ID_233943154 m1A Human chr5 + 61073171 61073169 61073172 GAGAAAAGAATTGTAGAAGCAGCAAATAAAAAAGAAGTAGACTATGAAGCAGGGGATATTCCAAC GAGAAAAGAATTGTAGAAGCAGCAAATAAAA___AAGTAGACTATGAAGCAGGGGATATTCCAAC AAAG A NDUFAF2 Ensembl:ENSG00000164182 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:61073075..61073200 26863196 MeRIP-seq:(Medium) rs949731001 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_643959,Human_RBP_ID_1997062,Human_RBP_ID_5617212,Human_RBP_ID_7453074,Human_RBP_ID_9349586,Human_RBP_ID_15476487 Human_Splice_Rec_654436,Human_Splice_Rec_654437,Human_Splice_Rec_654446,Human_Splice_Rec_654447,Human_Splice_Rec_654450,Human_Splice_Rec_654451 RMVar_hsa_circ_348895 77223 RMVar_ID_77223 Human_SNP_ID_233962420 m1A Human chr5 - 61159606 61159606 61159606 GGAAAAGTGACTTTAGATTATGAACTCAATTCAAATGAACTCTATTTAAAATGGGGTCCTATTTT GGAAAAGTGACTTTAGATTATGAACTCAATTCCAATGAACTCTATTTAAAATGGGGTCCTATTTT T G SMIM15 Ensembl:ENSG00000188725 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:61159351..61159850 32194978 MeRIP-seq:(Medium) rs771584172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_644008 Human_miRNA_ID_1788333 77224 RMVar_ID_77224 Human_SNP_ID_234005947 m1A Human chr5 + 61332354 61332327 61332354 GGCCGGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCCGG___________________________GCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCGGCGGCGGCGGCGGCGGGGGCAGCA G ZSWIM6 Ensembl:ENSG00000130449 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:61332254..61332459 26863196 MeRIP-seq:(Medium) rs1238074721 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_164991,Human_RBP_ID_22612530 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_85599,RMVar_hsa_circ_231635 77225 RMVar_ID_77225 Human_SNP_ID_234005951 m1A Human chr5 + 61332354 61332330 61332354 GGCCGGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCCGGGCG________________________GCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCGGCGGCGGCGGCGGGGGCAGCA G ZSWIM6 Ensembl:ENSG00000130449 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:61332254..61332459 26863196 MeRIP-seq:(Medium) rs1216384783 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_164991,Human_RBP_ID_22612530 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_85599,RMVar_hsa_circ_231635 77226 RMVar_ID_77226 Human_SNP_ID_234005953 m1A Human chr5 + 61332354 61332333 61332354 GGCCGGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCCGGGCGGCG_____________________GCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCGGCGGCGGCGGGGGCAGCA G ZSWIM6 Ensembl:ENSG00000130449 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:61332254..61332459 26863196 MeRIP-seq:(Medium) rs1243690822 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_164991,Human_RBP_ID_22612530 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_85599,RMVar_hsa_circ_231635 77227 RMVar_ID_77227 Human_SNP_ID_234005973 m1A Human chr5 + 61332354 61332354 61332354 GGCCGGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC GGCCGGGCGGCGGCGGCGGCGGCGGGGGCAGCGGCGGCGGCGGCGGCGGCGCGGGTGGCGGCTAC A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:61332254..61332459 26863196 MeRIP-seq:(Medium) rs1456197449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_164991,Human_RBP_ID_22612530 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_85599,RMVar_hsa_circ_231635 77228 RMVar_ID_77228 Human_SNP_ID_234005983 m1A Human chr5 - 61332377 61332359 61332377 GGGCCTGGCCGACAGGCAGAGCTGTAGCCGCCACCCGCGCCGCCGCCGCCGCCGCTGCTGCCCCC GGGCCTGGCCGACAGGCAGAGCTGTAGCCGCC__________________GCCGCTGCTGCCCCC CGGCGGCGGCGGCGCGGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr5:61332257..61332655;chr5:61332267..61332401;chr5:61332327..61332735 26863196 MeRIP-seq:(Medium) rs1331178503 Functional Loss DEL dbSNP153 33..50 33 - - - 77229 RMVar_ID_77229 Human_SNP_ID_234005990 m1A Human chr5 - 61332377 61332377 61332377 GGGCCTGGCCGACAGGCAGAGCTGTAGCCGCCACCCGCGCCGCCGCCGCCGCCGCTGCTGCCCCC GGGCCTGGCCGACAGGCAGAGCTGTAGCCGCCCCCCGCGCCGCCGCCGCCGCCGCTGCTGCCCCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr5:61332257..61332655;chr5:61332267..61332401;chr5:61332327..61332735 26863196 MeRIP-seq:(Medium) rs1010170694 Functional Loss SNV dbSNP153 33..33 33 - - - 77230 RMVar_ID_77230 Human_SNP_ID_234006082 m1A Human chr5 + 61332580 61332580 61332580 GCGCGTGGAGGAGCGCTTTGAGCGCATCCCGGAGCCGGTGCAGCGCCGCATAGTCTATTGGTCCT GCGCGTGGAGGAGCGCTTTGAGCGCATCCCGGGGCCGGTGCAGCGCCGCATAGTCTATTGGTCCT A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:61332267..61332714;chr5:61332271..61332719 26863196 MeRIP-seq:(Medium) rs746825579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18501721 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_85599,RMVar_hsa_circ_231635 77231 RMVar_ID_77231 Human_SNP_ID_234024959 m1A Human chr5 + 61408818 61408818 61408818 GCTTCCCACCAGTGGGTTTGTCTGAACTGTTTAGGAATGCGGCCGCGGTCGCCAGCTGACGTCAG GCTTCCCACCAGTGGGTTTGTCTGAACTGTTTGGGAATGCGGCCGCGGTCGCCAGCTGACGTCAG A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:61408816..61408988 26863196 MeRIP-seq:(Medium) rs1418993876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15478624 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 77232 RMVar_ID_77232 Human_SNP_ID_234237032 m1A Human chr5 - 62306269 62306267 62306269 CGGAGGCCCCGGGCCTGCAGGCCGGCAGGAGGACGCGCACGCCGGGTAGTCGGGGTGAAGCTAGG CGGAGGCCCCGGGCCTGCAGGCCGGCAGGAGG__GCGCACGCCGGGTAGTCGGGGTGAAGCTAGG CGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:62306182..62306490;chr5:62306182..62306367 26863196 MeRIP-seq:(Medium) rs1241177664 Functional Loss DEL dbSNP153 33..34 33 - - - 77233 RMVar_ID_77233 Human_SNP_ID_234260348 m1A Human chr5 - 62403726 62403726 62403726 GTCGGGGGCCATCGGCCGCCGCCGCGGGCGGCAGGAGCAGCGCCGGGAGCTGAAGAGCGCTGGAG GTCGGGGGCCATCGGCCGCCGCCGCGGGCGGCCGGAGCAGCGCCGGGAGCTGAAGAGCGCTGGAG T G DIMT1 Ensembl:ENSG00000086189 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:62403342..62403889 26863196 MeRIP-seq:(Medium) rs367686764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249862,Human_RBP_ID_4835268,Human_RBP_ID_19124447,Human_RBP_ID_23050401 Human_Splice_Rec_654959,Human_Splice_Rec_654991,Human_Splice_Rec_655015,Human_Splice_Rec_655035,Human_Splice_Rec_655053 RMVar_hsa_circ_231699,RMVar_hsa_circ_81284 77234 RMVar_ID_77234 Human_SNP_ID_234854248 m1A Human chr5 + 64769026 64769026 64769026 TGTTTGGTGTCCCTGTCTTGCGTGATATTGACAAACTGAAGCTTTCCTGCACCACTGGACTTAAG TGTTTGGTGTCCCTGTCTTGCGTGATATTGACCAACTGAAGCTTTCCTGCACCACTGGACTTAAG A C CWC27 Ensembl:ENSG00000153015 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:64768975..64769129 26863196 MeRIP-seq:(Medium) rs903389815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1656223,Human_RBP_ID_1997533,Human_RBP_ID_4845739 77235 RMVar_ID_77235 Human_SNP_ID_234854249 m1A Human chr5 + 64769026 64769026 64769026 TGTTTGGTGTCCCTGTCTTGCGTGATATTGACAAACTGAAGCTTTCCTGCACCACTGGACTTAAG TGTTTGGTGTCCCTGTCTTGCGTGATATTGACTAACTGAAGCTTTCCTGCACCACTGGACTTAAG A T CWC27 Ensembl:ENSG00000153015 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:64768975..64769129 26863196 MeRIP-seq:(Medium) rs903389815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1656223,Human_RBP_ID_1997533,Human_RBP_ID_4845739 77236 RMVar_ID_77236 Human_SNP_ID_234854251 m1A Human chr5 - 64769030 64769030 64769030 CTTCCTTAAGTCCAGTGGTGCAGGAAAGCTTCAGTTTGTCAATATCACGCAAGACAGGGACACCA CTTCCTTAAGTCCAGTGGTGCAGGAAAGCTTCGGTTTGTCAATATCACGCAAGACAGGGACACCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr5:64768979..64769129;chr5:64768979..64781970 26863196,32194978 MeRIP-seq:(Medium) rs544511154 Functional Loss SNV dbSNP153 33..33 33 - - - 77237 RMVar_ID_77237 Human_SNP_ID_234854253 m1A Human chr5 + 64769047 64769047 64769047 GTGATATTGACAAACTGAAGCTTTCCTGCACCACTGGACTTAAGGAAGAGTGTACTCGTAGGCGG GTGATATTGACAAACTGAAGCTTTCCTGCACCGCTGGACTTAAGGAAGAGTGTACTCGTAGGCGG A G CWC27 Ensembl:ENSG00000153015 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:64768959..64769079 26863410 MeRIP-seq:(Medium) rs1173714379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_644432,Human_RBP_ID_1656223,Human_RBP_ID_1997534,Human_RBP_ID_4845739,Human_RBP_ID_5427429,Human_RBP_ID_5476829,Human_RBP_ID_5611154,Human_RBP_ID_9178898 77238 RMVar_ID_77238 Human_SNP_ID_234862451 m1A Human chr5 - 64804330 64804330 64804330 ACTTCTCCTTCTCCAGCTGATTTAACATTCGCACTTGTGTCCTTTTTTAATTTTTTGGCAATTCT ACTTCTCCTTCTCCAGCTGATTTAACATTCGCGCTTGTGTCCTTTTTTAATTTTTTGGCAATTCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:64804281..64804381 32194978 MeRIP-seq:(Medium) rs753811241 Functional Loss SNV dbSNP153 33..33 33 - - - 77239 RMVar_ID_77239 Human_SNP_ID_234941129 m1A Human chr5 - 65159495 65159495 65159495 CAGGGCATTCCTGACAGAGGACAAGTGTGTGCAGTCACAGGGGCATGGAGGCAGTTTGCTATCGC CAGGGCATTCCTGACAGAGGACAAGTGTGTGCGGTCACAGGGGCATGGAGGCAGTTTGCTATCGC T C ADAMTS6 Ensembl:ENSG00000049192 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:65159447..65159560 26863196 MeRIP-seq:(Medium) rs1190762603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231783,RMVar_hsa_circ_106549 77240 RMVar_ID_77240 Human_SNP_ID_234941130 m1A Human chr5 - 65159495 65159495 65159495 CAGGGCATTCCTGACAGAGGACAAGTGTGTGCAGTCACAGGGGCATGGAGGCAGTTTGCTATCGC CAGGGCATTCCTGACAGAGGACAAGTGTGTGCCGTCACAGGGGCATGGAGGCAGTTTGCTATCGC T G ADAMTS6 Ensembl:ENSG00000049192 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:65159447..65159560 26863196 MeRIP-seq:(Medium) rs1190762603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231783,RMVar_hsa_circ_106549 77241 RMVar_ID_77241 Human_SNP_ID_234997037 m1A Human chr5 - 65402102 65402102 65402102 AAGTGGTAAACTTGGAAGATGAGCGATGGTAGAGAGTGCAATGCTTGAAATTAGTAATGACAAGG AAGTGGTAAACTTGGAAGATGAGCGATGGTAGGGAGTGCAATGCTTGAAATTAGTAATGACAAGG T C ADAMTS6 Ensembl:ENSG00000049192 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:65402051..65402219 26863196 MeRIP-seq:(Medium) rs1471864511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111326,RMVar_hsa_circ_328090,RMVar_hsa_circ_125942,RMVar_hsa_circ_122319,RMVar_hsa_circ_231791,RMVar_hsa_circ_231792,RMVar_hsa_circ_231790,RMVar_hsa_circ_45388,RMVar_hsa_circ_231793,RMVar_hsa_circ_369761,RMVar_hsa_circ_117098,RMVar_hsa_circ_231797,RMVar_hsa_circ_76430,RMVar_hsa_circ_231802,RMVar_hsa_circ_371899,RMVar_hsa_circ_231806,RMVar_hsa_circ_231807,RMVar_hsa_circ_327086,RMVar_hsa_circ_32895,RMVar_hsa_circ_285285,RMVar_hsa_circ_101055,RMVar_hsa_circ_96491,RMVar_hsa_circ_125380,RMVar_hsa_circ_231815,RMVar_hsa_circ_231816,RMVar_hsa_circ_231817,RMVar_hsa_circ_231819,RMVar_hsa_circ_111383,RMVar_hsa_circ_115178,RMVar_hsa_circ_231820,RMVar_hsa_circ_330584,RMVar_hsa_circ_231818,RMVar_hsa_circ_23209,RMVar_hsa_circ_231824,RMVar_hsa_circ_338832,RMVar_hsa_circ_296137,RMVar_hsa_circ_231825 77242 RMVar_ID_77242 Human_SNP_ID_235036060 m1A Human chr5 + 65563350 65563350 65563350 CGGAAAGTGGTAGCGATTTTCAGCAGAGACGTAGAAGGCGCCGGGACCCGGAGGAACCGGAAAAA CGGAAAGTGGTAGCGATTTTCAGCAGAGACGTTGAAGGCGCCGGGACCCGGAGGAACCGGAAAAA A T PPWD1 Ensembl:ENSG00000113593 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:65563301..65563528 26863196 MeRIP-seq:(Medium) rs1482297502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249960,Human_RBP_ID_839107,Human_RBP_ID_4835637,Human_RBP_ID_9399115,Human_RBP_ID_15488612,Human_RBP_ID_22301996,Human_RBP_ID_24547928,Human_RBP_ID_27825416 RMVar_hsa_circ_101184,RMVar_hsa_circ_231843,RMVar_hsa_circ_95606,RMVar_hsa_circ_231844 77243 RMVar_ID_77243 Human_SNP_ID_235036061 m1A Human chr5 + 65563353 65563353 65563353 AAAGTGGTAGCGATTTTCAGCAGAGACGTAGAAGGCGCCGGGACCCGGAGGAACCGGAAAAAACA AAAGTGGTAGCGATTTTCAGCAGAGACGTAGAGGGCGCCGGGACCCGGAGGAACCGGAAAAAACA A G PPWD1 Ensembl:ENSG00000113593 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:65563285..65563508 26863196 MeRIP-seq:(Medium) rs775018345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249960,Human_RBP_ID_839107,Human_RBP_ID_4835637,Human_RBP_ID_9399115,Human_RBP_ID_15488612,Human_RBP_ID_22301996,Human_RBP_ID_24547928,Human_RBP_ID_27825416 RMVar_hsa_circ_101184,RMVar_hsa_circ_231843,RMVar_hsa_circ_95606,RMVar_hsa_circ_231844 77244 RMVar_ID_77244 Human_SNP_ID_235073893 m1A Human chr5 + 65722069 65722062 65722070 CAAACTTCCCCGGCCCCTAGGCCGTAGACCCCAGAACCCACCAGGCTGTGCTCTCTCTCAGGCGG CAAACTTCCCCGGCCCCTAGGCCGTA________AACCCACCAGGCTGTGCTCTCTCTCAGGCGG AGACCCCAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:65722023..65722090 26863196 MeRIP-seq:(Medium) rs571430955 Functional Loss DEL dbSNP153 27..34 33 - - - 77245 RMVar_ID_77245 Human_SNP_ID_235074013 m1A Human chr5 + 65722327 65722327 65722327 CGCCCAGGCGCTGCCGCCCGCCTCGCCGCCCCACGCCGAAGGACCACGCGCCCGCCGCCGCCAGC CGCCCAGGCGCTGCCGCCCGCCTCGCCGCCCCCCGCCGAAGGACCACGCGCCCGCCGCCGCCAGC A C NLN Ensembl:ENSG00000123213 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr5:65722226..65722366;chr5:65722226..65722425 26863410 MeRIP-seq:(Medium) rs536374883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845192,Human_RBP_ID_9399120 Human_Splice_Rec_656337,Human_Splice_Rec_656361,Human_Splice_Rec_656383,Human_Splice_Rec_656389 RMVar_hsa_circ_78481,RMVar_hsa_circ_231880 77246 RMVar_ID_77246 Human_SNP_ID_235122648 m1A Human chr5 + 65926107 65926103 65926107 AGAGGGTTCGAGGGCGAGTAGGGAAAGCGGGGAGGGACGGACGGAAGGACGGACGGCCCGACGGA AGAGGGTTCGAGGGCGAGTAGGGAAAGCG____GGGACGGACGGAAGGACGGACGGCCCGACGGA GGGGA G lnc-NLN-3 RNACentral:URS00009C13CC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:65925921..65926250 26863196 MeRIP-seq:(Medium) rs1394660752 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4835940,Human_RBP_ID_8891233 77247 RMVar_ID_77247 Human_SNP_ID_235122650 m1A Human chr5 + 65926119 65926108 65926120 GGCGAGTAGGGAAAGCGGGGAGGGACGGACGGAAGGACGGACGGCCCGACGGACGGCCCGGGGAG GGCGAGTAGGGAAAGCGGGGAG____________GGACGGACGGCCCGACGGACGGCCCGGGGAG GGGACGGACGGAA G lnc-NLN-3 RNACentral:URS00009C13CC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:65925884..65926325 26863196 MeRIP-seq:(Medium) rs892467588 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_4835942 77248 RMVar_ID_77248 Human_SNP_ID_235122657 m1A Human chr5 + 65926119 65926119 65926119 GGCGAGTAGGGAAAGCGGGGAGGGACGGACGGAAGGACGGACGGCCCGACGGACGGCCCGGGGAG GGCGAGTAGGGAAAGCGGGGAGGGACGGACGGCAGGACGGACGGCCCGACGGACGGCCCGGGGAG A C lnc-NLN-3 RNACentral:URS00009C13CC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:65925884..65926325 26863196 MeRIP-seq:(Medium) rs189444895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4835942 77249 RMVar_ID_77249 Human_SNP_ID_235144572 m1A Human chr5 + 66005191 66005191 66005191 GGTGATAGTGATGGACATAGTGAGATGAGGACAGCCCCTGGATATGCTTGAAGGTGGAATCAATA GGTGATAGTGATGGACATAGTGAGATGAGGACGGCCCCTGGATATGCTTGAAGGTGGAATCAATA A G ERBIN Ensembl:ENSG00000112851 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:66005141..66005296 26863196 MeRIP-seq:(Medium) rs1561361545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7459541,Human_RBP_ID_15492101 RMVar_hsa_circ_6354,RMVar_hsa_circ_285872,RMVar_hsa_circ_334291,RMVar_hsa_circ_231910,RMVar_hsa_circ_293807,RMVar_hsa_circ_272026,RMVar_hsa_circ_31027,RMVar_hsa_circ_114439,RMVar_hsa_circ_6902,RMVar_hsa_circ_54254,RMVar_hsa_circ_231911,RMVar_hsa_circ_231913,RMVar_hsa_circ_231915,RMVar_hsa_circ_231916,RMVar_hsa_circ_231914,RMVar_hsa_circ_231912,RMVar_hsa_circ_231919,RMVar_hsa_circ_359345,RMVar_hsa_circ_367799,RMVar_hsa_circ_369516,RMVar_hsa_circ_313838,RMVar_hsa_circ_231921,RMVar_hsa_circ_44317,RMVar_hsa_circ_231920,RMVar_hsa_circ_58603,RMVar_hsa_circ_44695 77250 RMVar_ID_77250 Human_SNP_ID_235164291 m1A Human chr5 + 66078476 66078476 66078476 AATATTGAACATGGACAAGCAGTGTCCTTGCTAAAAACTTTCCAGAATACAGTTGAACTCATCAT AATATTGAACATGGACAAGCAGTGTCCTTGCTGAAAACTTTCCAGAATACAGTTGAACTCATCAT A G ERBIN Ensembl:ENSG00000112851 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:66078426..66078525 32194978 MeRIP-seq:(Medium) rs1485469870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1998111,Human_RBP_ID_8891284,Human_RBP_ID_15493299,Human_RBP_ID_17302720,Human_RBP_ID_17414216,Human_RBP_ID_25932524 Human_Splice_Rec_656510,Human_Splice_Rec_656558,Human_Splice_Rec_656596,Human_Splice_Rec_656642,Human_Splice_Rec_656688,Human_Splice_Rec_656736,Human_Splice_Rec_656786,Human_Splice_Rec_656830,Human_Splice_Rec_656844,Human_Splice_Rec_656854,Human_Splice_Rec_656856 77251 RMVar_ID_77251 Human_SNP_ID_235180221 m1A Human chr5 + 66144380 66144380 66144380 AGCGGGAAGGCAACGGCAGCGGGATCGGGATGAACAGCGGCGGCGGCTTCGGTTTGGGCTTAGGC AGCGGGAAGGCAACGGCAGCGGGATCGGGATGCACAGCGGCGGCGGCTTCGGTTTGGGCTTAGGC A C SREK1 Ensembl:ENSG00000153914 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:66144251..66144492 26863196 MeRIP-seq:(Medium) rs1421176326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250824,Human_RBP_ID_788809,Human_RBP_ID_4845744,Human_RBP_ID_15493536,Human_RBP_ID_18424959,Human_RBP_ID_22099422,Human_RBP_ID_23050134,Human_RBP_ID_23116216 Human_Splice_Rec_656925 77252 RMVar_ID_77252 Human_SNP_ID_235186657 m1A Human chr5 + 66170151 66170151 66170151 AACGCTCTAAATCAAGGGAGAGACGGAAGTCAAGGAGTCGTTCGCATTCACGGTGAGTTTTAGAG AACGCTCTAAATCAAGGGAGAGACGGAAGTCATGGAGTCGTTCGCATTCACGGTGAGTTTTAGAG A T SREK1 Ensembl:ENSG00000153914 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:66170101..66170175 26863196 MeRIP-seq:(Medium) rs1304929501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250235,Human_RBP_ID_839407,Human_RBP_ID_7460446,Human_RBP_ID_24547929,Human_RBP_ID_27826407 Human_Splice_Rec_656891,Human_Splice_Rec_656917,Human_Splice_Rec_656941,Human_Splice_Rec_656965,Human_Splice_Rec_656983,Human_Splice_Rec_657005,Human_Splice_Rec_657023,Human_Splice_Rec_657025,Human_Splice_Rec_657037 RMVar_hsa_circ_8740,RMVar_hsa_circ_273939,RMVar_hsa_circ_231952,RMVar_hsa_circ_371392,RMVar_hsa_circ_45091,RMVar_hsa_circ_345387,RMVar_hsa_circ_231954,RMVar_hsa_circ_369183,RMVar_hsa_circ_119858,RMVar_hsa_circ_231958 77253 RMVar_ID_77253 Human_SNP_ID_235186850 m1A Human chr5 + 66170748 66170725 66170749 ACAAGGAACGGGAAAAGGACCGGGAAAAAGACAAGGAAAAGGACAGAGAGAGAGAACGGGAAAAA ACAAGGAACG________________________GGAAAAGGACAGAGAGAGAGAACGGGAAAAA GGGAAAAGGACCGGGAAAAAGACAA G SREK1 Ensembl:ENSG00000153914 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:66170647..66170819 26863196 MeRIP-seq:(Medium) rs1177652618 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_250236,Human_RBP_ID_788153,Human_RBP_ID_840215,Human_RBP_ID_23050405,Human_RBP_ID_24547933,Human_RBP_ID_24554369,Human_RBP_ID_26350868 RMVar_hsa_circ_8740,RMVar_hsa_circ_273939,RMVar_hsa_circ_231952,RMVar_hsa_circ_371392,RMVar_hsa_circ_231954,RMVar_hsa_circ_369183,RMVar_hsa_circ_119858,RMVar_hsa_circ_231958 77254 RMVar_ID_77254 Human_SNP_ID_235186868 m1A Human chr5 + 66170755 66170755 66170755 ACGGGAAAAGGACCGGGAAAAAGACAAGGAAAAGGACAGAGAGAGAGAACGGGAAAAAGAGCATG ACGGGAAAAGGACCGGGAAAAAGACAAGGAAAGGGACAGAGAGAGAGAACGGGAAAAAGAGCATG A G SREK1 Ensembl:ENSG00000153914 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:66170576..66170950 26863196 MeRIP-seq:(Medium) rs751724757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250236,Human_RBP_ID_788153,Human_RBP_ID_840215,Human_RBP_ID_5617221,Human_RBP_ID_23050405,Human_RBP_ID_24547933,Human_RBP_ID_24554369,Human_RBP_ID_26350869,Human_RBP_ID_27826409 RMVar_hsa_circ_8740,RMVar_hsa_circ_273939,RMVar_hsa_circ_231952,RMVar_hsa_circ_371392,RMVar_hsa_circ_231954,RMVar_hsa_circ_369183,RMVar_hsa_circ_119858,RMVar_hsa_circ_231958 77255 RMVar_ID_77255 Human_SNP_ID_235346004 m1A Human chr5 + 66839044 66839044 66839044 CTAGGAATTTAGAAATGAGGAGGTGGTAGATGATGCTGCTGGACCGAGGTGGTGACAGTGAAATG CTAGGAATTTAGAAATGAGGAGGTGGTAGATGCTGCTGCTGGACCGAGGTGGTGACAGTGAAATG A C MAST4 Ensembl:ENSG00000069020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:66839028..66839144 26863196 MeRIP-seq:(Medium) rs1432792580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69184,RMVar_hsa_circ_53968,RMVar_hsa_circ_58531 77256 RMVar_ID_77256 Human_SNP_ID_235382287 m1A Human chr5 + 66984689 66984689 66984689 GACTACAGGGGTAAATAGTGAAATTGGAGAGAAGTAGATGGATTCAGGCTGTGTTCTGAGGGGGA GACTACAGGGGTAAATAGTGAAATTGGAGAGAGGTAGATGGATTCAGGCTGTGTTCTGAGGGGGA A G MAST4 Ensembl:ENSG00000069020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:66984672..66984821 26863196 MeRIP-seq:(Medium) rs1333473600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39589 77257 RMVar_ID_77257 Human_SNP_ID_235694690 m1A Human chr5 + 68215810 68215810 68215810 TTGGAGGAAGCAGCGGCAGCGGCGAGGGCGGCAGGCTAGCTGTCGGAGACGGCAAGCACGGATCG TTGGAGGAAGCAGCGGCAGCGGCGAGGGCGGCCGGCTAGCTGTCGGAGACGGCAAGCACGGATCG A C PIK3R1 Ensembl:ENSG00000145675 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:68215771..68215924;chr5:68215760..68215942 26863196 MeRIP-seq:(Medium) rs1302997357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943361 77258 RMVar_ID_77258 Human_SNP_ID_235910683 m1A Human chr5 - 69129556 69129555 69129556 ATTTCATGGATTCCATTTGTTTTGTCATAGCCAGAACATCATGAAATCCAGTACTTAGGCCAGAC ATTTCATGGATTCCATTTGTTTTGTCATAGCC_GAACATCATGAAATCCAGTACTTAGGCCAGAC CT C AC010273.2 Ensembl:ENSG00000248664 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:69128043..69130378 32194978 MeRIP-seq:(Medium) rs1457740261 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_15636 77259 RMVar_ID_77259 Human_SNP_ID_235920030 m1A Human chr5 - 69167198 69167181 69167199 GGAGAAGCAGAACACCGGAGGCCCGACCAGCCAAGGACCTACACCCAGCAGAAACCAACAGCCGT GGAGAAGCAGAACACCGGAGGCCCGACCAGC__________________AGAAACCAACAGCCGT TGCTGGGTGTAGGTCCTTG T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr5:69167151..69167349;chr5:69167151..69167327 26863196 MeRIP-seq:(Medium) rs1362227548 Functional Loss DEL dbSNP153 32..49 33 - - - 77260 RMVar_ID_77260 Human_SNP_ID_235920040 m1A Human chr5 - 69167205 69167205 69167205 TCAGCGGGGAGAAGCAGAACACCGGAGGCCCGACCAGCCAAGGACCTACACCCAGCAGAAACCAA TCAGCGGGGAGAAGCAGAACACCGGAGGCCCGGCCAGCCAAGGACCTACACCCAGCAGAAACCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:69167120..69167314;chr5:69167126..69167467 26863196 MeRIP-seq:(Medium) rs1267444095 Functional Loss SNV dbSNP153 33..33 33 - - - 77261 RMVar_ID_77261 Human_SNP_ID_235920082 m1A Human chr5 - 69167285 69167285 69167285 AGGCCGCGTTAGTTCGCAGTCCGAAGCGGCTCACCCTGGTGACTCGGAGCGCCATGGCTTCCTCT AGGCCGCGTTAGTTCGCAGTCCGAAGCGGCTCTCCCTGGTGACTCGGAGCGCCATGGCTTCCTCT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:69167126..69167345 26863196 MeRIP-seq:(Medium) rs750802735 Functional Loss SNV dbSNP153 33..33 33 - - - 77262 RMVar_ID_77262 Human_SNP_ID_235920301 m1A Human chr5 - 69167904 69167897 69167904 GCCTTATTTTCAGCATTAATTTTCGAGTTCTGAAAGAAGCAAGACCACTTTAAGAGCTGATCCAC GCCTTATTTTCAGCATTAATTTTCGAGTTCTG_______CAAGACCACTTTAAGAGCTGATCCAC GCTTCTTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr5:69167901..69167925;chr5:69167901..69168025;chr5:69167901..69168000 26863196 MeRIP-seq:(Medium) rs775282499 Functional Loss DEL dbSNP153 33..39 33 - - - 77263 RMVar_ID_77263 Human_SNP_ID_235920306 m1A Human chr5 + 69167909 69167909 69167909 TCAGCTCTTAAAGTGGTCTTGCTTCTTTCAGAACTCGAAAATTAATGCTGAAAATAAGGCGAAGA TCAGCTCTTAAAGTGGTCTTGCTTCTTTCAGACCTCGAAAATTAATGCTGAAAATAAGGCGAAGA A C CCNB1 Ensembl:ENSG00000134057 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:69167901..69174283 32194978 MeRIP-seq:(Medium) rs1296233724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1657089,Human_RBP_ID_4845751,Human_RBP_ID_9397852 Human_Splice_Rec_657996,Human_Splice_Rec_658010,Human_Splice_Rec_658026,Human_Splice_Rec_658034,Human_Splice_Rec_658048 RMVar_hsa_circ_232012,RMVar_hsa_circ_308980 77264 RMVar_ID_77264 Human_SNP_ID_235920334 m1A Human chr5 - 69167966 69167966 69167966 CGGGCTTGGAGGTTGCAGCAGGGGCCGTAGGAACGCGCTTTGCGCCTGCCATGTTGATCTTCGCC CGGGCTTGGAGGTTGCAGCAGGGGCCGTAGGAGCGCGCTTTGCGCCTGCCATGTTGATCTTCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:69167901..69168025 26863196 MeRIP-seq:(Medium) rs369506933 Functional Loss SNV dbSNP153 33..33 33 - - - 77265 RMVar_ID_77265 Human_SNP_ID_235922037 m1A Human chr5 + 69174301 69174301 69174301 CCAAAATACCTACTGGGTCGGGAAGTCACTGGAAACATGAGAGCCATCCTAATTGACTGGCTAGT CCAAAATACCTACTGGGTCGGGAAGTCACTGGCAACATGAGAGCCATCCTAATTGACTGGCTAGT A C CCNB1 Ensembl:ENSG00000134057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:69174222..69174431 26863196 MeRIP-seq:(Medium) rs755245029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75348,Human_RBP_ID_1657114,Human_RBP_ID_1998566,Human_RBP_ID_3776053,Human_RBP_ID_7463004,Human_RBP_ID_15500556,Human_RBP_ID_18846081,Human_RBP_ID_24113993 Human_Splice_Rec_658002,Human_Splice_Rec_658016,Human_Splice_Rec_658040,Human_Splice_Rec_658054 Human_miRNA_ID_2971237 RMVar_hsa_circ_232012,RMVar_hsa_circ_232015,RMVar_hsa_circ_283347,RMVar_hsa_circ_276732,RMVar_hsa_circ_232014,RMVar_hsa_circ_232016,RMVar_hsa_circ_322080,RMVar_hsa_circ_326850,RMVar_hsa_circ_232017 77266 RMVar_ID_77266 Human_SNP_ID_235922248 m1A Human chr5 + 69174925 69174925 69174925 AGAAGATGCTGCAGCTGGTTGGTGTCACTGCCATGTTTATTGCAAGCAAATATGAAGAAATGTAC AGAAGATGCTGCAGCTGGTTGGTGTCACTGCCGTGTTTATTGCAAGCAAATATGAAGAAATGTAC A G CCNB1 Ensembl:ENSG00000134057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:69174840..69175074 26863196 MeRIP-seq:(Medium) rs772787353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1657119,Human_RBP_ID_1998570,Human_RBP_ID_7463007,Human_RBP_ID_9179620,Human_RBP_ID_9397862,Human_RBP_ID_18846085,Human_RBP_ID_19014886,Human_RBP_ID_22099435,Human_RBP_ID_22460071,Human_RBP_ID_22512603,Human_RBP_ID_22680460,Human_RBP_ID_22828708,Human_RBP_ID_24113999,Human_RBP_ID_27083713 Human_Splice_Rec_658004,Human_Splice_Rec_658018,Human_Splice_Rec_658032,Human_Splice_Rec_658042,Human_Splice_Rec_658056 Human_miRNA_ID_2456686,Human_miRNA_ID_2456687,Human_miRNA_ID_2461597,Human_miRNA_ID_2461598,Human_miRNA_ID_2634255,Human_miRNA_ID_2634256,Human_miRNA_ID_2636942,Human_miRNA_ID_2636943 RMVar_hsa_circ_232012,RMVar_hsa_circ_108832,RMVar_hsa_circ_232015,RMVar_hsa_circ_283347,RMVar_hsa_circ_322080,RMVar_hsa_circ_232017,RMVar_hsa_circ_125567,RMVar_hsa_circ_270763,RMVar_hsa_circ_232019,RMVar_hsa_circ_232021,RMVar_hsa_circ_98510,RMVar_hsa_circ_232020,RMVar_hsa_circ_232018 77267 RMVar_ID_77267 Human_SNP_ID_235926444 m1A Human chr5 + 69189729 69189729 69189729 GGCAGGCGGGCCACCGCAGGTCGCCGGCGCCCAGGCGGCGTGCAGCGAGGACCGCATGACCCTGC GGCAGGCGGGCCACCGCAGGTCGCCGGCGCCCGGGCGGCGTGCAGCGAGGACCGCATGACCCTGC A G CENPH Ensembl:ENSG00000153044 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:69189626..69189775 32194978 MeRIP-seq:(Medium) rs1388942127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250230,Human_RBP_ID_4845753,Human_RBP_ID_9335237,Human_RBP_ID_22460074 Human_Splice_Rec_658065,Human_Splice_Rec_658079,Human_Splice_Rec_658095,Human_Splice_Rec_658105,Human_Splice_Rec_658113 RMVar_hsa_circ_103108,RMVar_hsa_circ_232023 77268 RMVar_ID_77268 Human_SNP_ID_235934059 m1A Human chr5 - 69217856 69217856 69217856 GCGACAAATTGCTTTACCTGAACGACCCTACTAGCAGACGCCATCTTGCTGCCCATCATGACCCC GCGACAAATTGCTTTACCTGAACGACCCTACTGGCAGACGCCATCTTGCTGCCCATCATGACCCC T C lnc-CCDC125-10 RNACentral:URS00008B9950 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:69217787..69218108;chr5:69217808..69218087 26863196 MeRIP-seq:(Medium) rs752013383 Functional Loss SNV dbSNP153 33..33 33 - - - 77269 RMVar_ID_77269 Human_SNP_ID_235934066 m1A Human chr5 - 69217873 69217873 69217873 GCCCAAGATGCGGAAACGCGACAAATTGCTTTACCTGAACGACCCTACTAGCAGACGCCATCTTG GCCCAAGATGCGGAAACGCGACAAATTGCTTTGCCTGAACGACCCTACTAGCAGACGCCATCTTG T C lnc-CCDC125-10 RNACentral:URS00008B9950 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:69217808..69217908 26863410 MeRIP-seq:(Medium) rs1375084959 Functional Loss SNV dbSNP153 33..33 33 - - - 77270 RMVar_ID_77270 Human_SNP_ID_235938143 m1A Human chr5 + 69235002 69235002 69235002 CGCCGGATGGCTCTGGACGTGAAGTCTCGGGCAAAGCGTTATGAGAAGCTGGACTTCCTTGGGGA CGCCGGATGGCTCTGGACGTGAAGTCTCGGGCTAAGCGTTATGAGAAGCTGGACTTCCTTGGGGA A T CDK7 Ensembl:ENSG00000134058 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:69234951..69235215 32194978 MeRIP-seq:(Medium) rs943322252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645334,Human_RBP_ID_4845757,Human_RBP_ID_8621005,Human_RBP_ID_23120191 Human_Splice_Rec_658155,Human_Splice_Rec_658159,Human_Splice_Rec_658191,Human_Splice_Rec_658199,Human_Splice_Rec_658215,Human_Splice_Rec_658217,Human_Splice_Rec_658239,Human_Splice_Rec_658249,Human_Splice_Rec_658259,Human_Splice_Rec_658275,Human_Splice_Rec_658295,Human_Splice_Rec_658311 RMVar_hsa_circ_86545,RMVar_hsa_circ_232027 77271 RMVar_ID_77271 Human_SNP_ID_235962682 m1A Human chr5 + 69332706 69332706 69332706 TCTCAAGGTCCGTGGCGGGGACCGGAGCCCGGACTCCAGCTCAGCGAACAGCACCCTCCTACCGC TCTCAAGGTCCGTGGCGGGGACCGGAGCCCGGCCTCCAGCTCAGCGAACAGCACCCTCCTACCGC A C RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr5:69332690..69332769;chr5:69332631..69332769 26863196 MeRIP-seq:(Medium) rs1385732536 Functional Loss SNV dbSNP153 33..33 33 - - - 77272 RMVar_ID_77272 Human_SNP_ID_235968424 m1A Human chr5 + 69355948 69355948 69355948 ACAGTCATACTCTTCATCATAGCCATCATACAATTGCTCTAAAAGAGATTTAGAATTGCTTGTTG ACAGTCATACTCTTCATCATAGCCATCATACAGTTGCTCTAAAAGAGATTTAGAATTGCTTGTTG A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:69355876..69355975 26863196 MeRIP-seq:(Medium) rs764326425 Functional Loss SNV dbSNP153 33..33 33 - - - 77273 RMVar_ID_77273 Human_SNP_ID_235968427 m1A Human chr5 - 69355955 69355955 69355955 AATATTTCAACAAGCAATTCTAAATCTCTTTTAGAGCAATTGTATGATGGCTATGATGAAGAGTA AATATTTCAACAAGCAATTCTAAATCTCTTTTGGAGCAATTGTATGATGGCTATGATGAAGAGTA T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:69355876..69355975 26863196 MeRIP-seq:(Medium) rs766153493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_658463,Human_Splice_Rec_658475,Human_Splice_Rec_658481,Human_Splice_Rec_658489 RMVar_hsa_circ_323024 77274 RMVar_ID_77274 Human_SNP_ID_235971203 m1A Human chr5 + 69366555 69366555 69366555 ACATTAATGTATTTCAGTCCTGATTTTGACGCAAGTTCTTTGCCTAGTGTGGTTTTTCCAACCCC ACATTAATGTATTTCAGTCCTGATTTTGACGCTAGTTCTTTGCCTAGTGTGGTTTTTCCAACCCC A T RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:69366436..69366630 26863196 MeRIP-seq:(Medium) rs566395252 Functional Loss SNV dbSNP153 33..33 33 - - - 77275 RMVar_ID_77275 Human_SNP_ID_235971206 m1A Human chr5 - 69366567 69366567 69366567 ACAGGTACACCAGGGGTTGGAAAAACCACACTAGGCAAAGAACTTGCGTCAAAATCAGGACTGAA ACAGGTACACCAGGGGTTGGAAAAACCACACTGGGCAAAGAACTTGCGTCAAAATCAGGACTGAA T C AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:69366473..69366600;chr5:69366454..69366630;chr5:69366446..69366600 26863196 MeRIP-seq:(Medium) rs370169491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1657229,Human_RBP_ID_1998654,Human_RBP_ID_4845760,Human_RBP_ID_7463569,Human_RBP_ID_15502072,Human_RBP_ID_17302008,Human_RBP_ID_17415202,Human_RBP_ID_18846190,Human_RBP_ID_25913204 Human_Splice_Rec_658460,Human_Splice_Rec_658461,Human_Splice_Rec_658468,Human_Splice_Rec_658469,Human_Splice_Rec_658472,Human_Splice_Rec_658473,Human_Splice_Rec_658486,Human_Splice_Rec_658487,Human_Splice_Rec_658491,Human_Splice_Rec_658494,Human_Splice_Rec_658495,Human_Splice_Rec_658498,Human_Splice_Rec_658499,Human_Splice_Rec_658502,Human_Splice_Rec_658503,Human_Splice_Rec_658506,Human_Splice_Rec_658507,Human_Splice_Rec_658510,Human_Splice_Rec_658511,Human_Splice_Rec_658514,Human_Splice_Rec_658515,Human_Splice_Rec_658518,Human_Splice_Rec_658519 RMVar_hsa_circ_323024 77276 RMVar_ID_77276 Human_SNP_ID_235971214 m1A Human chr5 + 69366583 69366583 69366583 ACGCAAGTTCTTTGCCTAGTGTGGTTTTTCCAACCCCTGGTGTACCTGTAAGACAAGCCACAGAA ACGCAAGTTCTTTGCCTAGTGTGGTTTTTCCACCCCCTGGTGTACCTGTAAGACAAGCCACAGAA A C RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:69355942..69366590 32194978 MeRIP-seq:(Medium) rs771375480 Functional Loss SNV dbSNP153 33..33 33 - - - 77277 RMVar_ID_77277 Human_SNP_ID_235971215 m1A Human chr5 + 69366583 69366583 69366583 ACGCAAGTTCTTTGCCTAGTGTGGTTTTTCCAACCCCTGGTGTACCTGTAAGACAAGCCACAGAA ACGCAAGTTCTTTGCCTAGTGTGGTTTTTCCATCCCCTGGTGTACCTGTAAGACAAGCCACAGAA A T RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:69355942..69366590 32194978 MeRIP-seq:(Medium) rs771375480 Functional Loss SNV dbSNP153 33..33 33 - - - 77278 RMVar_ID_77278 Human_SNP_ID_235972062 m1A Human chr5 - 69369284 69369284 69369284 CCGACCCTCGCGGGCGTTGCGGGAGGCGAGGGAGGGGACGCGGAACGTTAATTCCGTTGGCCTGA CCGACCCTCGCGGGCGTTGCGGGAGGCGAGGGGGGGGACGCGGAACGTTAATTCCGTTGGCCTGA T C AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:69369282..69369613 26863196 MeRIP-seq:(Medium) rs998004872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9437065 Human_Splice_Rec_658501 77279 RMVar_ID_77279 Human_SNP_ID_235972063 m1A Human chr5 - 69369284 69369284 69369284 CCGACCCTCGCGGGCGTTGCGGGAGGCGAGGGAGGGGACGCGGAACGTTAATTCCGTTGGCCTGA CCGACCCTCGCGGGCGTTGCGGGAGGCGAGGGCGGGGACGCGGAACGTTAATTCCGTTGGCCTGA T G AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:69369282..69369613 26863196 MeRIP-seq:(Medium) rs998004872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9437065 Human_Splice_Rec_658501 77280 RMVar_ID_77280 Human_SNP_ID_235972066 m1A Human chr5 - 69369288 69369288 69369288 GGAGCCGACCCTCGCGGGCGTTGCGGGAGGCGAGGGAGGGGACGCGGAACGTTAATTCCGTTGGC GGAGCCGACCCTCGCGGGCGTTGCGGGAGGCGGGGGAGGGGACGCGGAACGTTAATTCCGTTGGC T C AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:69369285..69369550 26863196 MeRIP-seq:(Medium) rs535861720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9437065 Human_Splice_Rec_658501 77281 RMVar_ID_77281 Human_SNP_ID_235972133 m1A Human chr5 - 69369443 69369443 69369443 ATCCTGCTCACCGGTCAGGGCGCGCGGCCGGGAGGGACTGGGCTGGGGCAGGCTGGGGGCGCAGA ATCCTGCTCACCGGTCAGGGCGCGCGGCCGGGGGGGACTGGGCTGGGGCAGGCTGGGGGCGCAGA T C AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:69369324..69369462 26863196 MeRIP-seq:(Medium) rs1321406499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838823,Human_RBP_ID_7463590,Human_RBP_ID_18424962,Human_RBP_ID_19125699,Human_RBP_ID_22099438 Human_Splice_Rec_658513 77282 RMVar_ID_77282 Human_SNP_ID_236018435 m1A Human chr5 + 69560295 69560295 69560295 CTGTGAGGCGCAGAGGTGGGGCAGGCCGTCTGACTAGCTAGGCGGCTGGGAGCGTTTTCGTGGCG CTGTGAGGCGCAGAGGTGGGGCAGGCCGTCTGGCTAGCTAGGCGGCTGGGAGCGTTTTCGTGGCG A G GTF2H2C Ensembl:ENSG00000183474 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:69560237..69560350;chr5:69560226..69560364 26863196 MeRIP-seq:(Medium) rs2666589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845764 77283 RMVar_ID_77283 Human_SNP_ID_236051261 m1A Human chr5 - 70077263 70077263 70077263 TCTCAACTGCCTCACCACCGTGCTGGCCTCCCACCCCCACCTCAGTCTTTTACAGATGGTTTTTC TCTCAACTGCCTCACCACCGTGCTGGCCTCCCCCCCCCACCTCAGTCTTTTACAGATGGTTTTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:70077216..70077281 26863196 MeRIP-seq:(Medium) rs1408096174 Functional Loss SNV dbSNP153 33..33 33 - - - 77284 RMVar_ID_77284 Human_SNP_ID_236182052 m1A Human chr5 + 71510167 71510167 71510167 ACTGGAAGAGAGAGTTCTCCAAGGGAGAAGACACCAGAGGTGATTGATGCTACTGAGGAAATAGA ACTGGAAGAGAGAGTTCTCCAAGGGAGAAGACGCCAGAGGTGATTGATGCTACTGAGGAAATAGA A G BDP1 Ensembl:ENSG00000145734 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:71510118..71510195 26863196 MeRIP-seq:(Medium) rs1374113211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75679,Human_RBP_ID_22364719,Human_RBP_ID_24547947,Human_RBP_ID_26352182 RMVar_hsa_circ_746,RMVar_hsa_circ_99788,RMVar_hsa_circ_267624,RMVar_hsa_circ_92883,RMVar_hsa_circ_266589,RMVar_hsa_circ_232195,RMVar_hsa_circ_68577,RMVar_hsa_circ_116406,RMVar_hsa_circ_24808,RMVar_hsa_circ_232198,RMVar_hsa_circ_127599,RMVar_hsa_circ_232200,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232206,RMVar_hsa_circ_232201,RMVar_hsa_circ_232202,RMVar_hsa_circ_344419,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_267014,RMVar_hsa_circ_232207,RMVar_hsa_circ_232204,RMVar_hsa_circ_232205,RMVar_hsa_circ_306242,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_30537,RMVar_hsa_circ_232213,RMVar_hsa_circ_232209,RMVar_hsa_circ_232211,RMVar_hsa_circ_232212,RMVar_hsa_circ_232210,RMVar_hsa_circ_363518,RMVar_hsa_circ_337416,RMVar_hsa_circ_356163,RMVar_hsa_circ_283938,RMVar_hsa_circ_232215,RMVar_hsa_circ_232217,RMVar_hsa_circ_232216,RMVar_hsa_circ_232214,RMVar_hsa_circ_232225,RMVar_hsa_circ_232221,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_120896,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232220,RMVar_hsa_circ_270747,RMVar_hsa_circ_332213,RMVar_hsa_circ_69265,RMVar_hsa_circ_232228,RMVar_hsa_circ_232226,RMVar_hsa_circ_232224,RMVar_hsa_circ_232227 77285 RMVar_ID_77285 Human_SNP_ID_236182295 m1A Human chr5 + 71510765 71510765 71510765 CAGAGGAGGTCAAGCCTGTAGGTAAAATGGAGACAGATTTGAAAGAAATTAGAGAAGAAATTTCC CAGAGGAGGTCAAGCCTGTAGGTAAAATGGAGTCAGATTTGAAAGAAATTAGAGAAGAAATTTCC A T BDP1 Ensembl:ENSG00000145734 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:71510578..71510884 26863196 MeRIP-seq:(Medium) rs747963045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8891652,Human_RBP_ID_18846337,Human_RBP_ID_24114446 Human_miRNA_ID_2046954 RMVar_hsa_circ_746,RMVar_hsa_circ_99788,RMVar_hsa_circ_267624,RMVar_hsa_circ_92883,RMVar_hsa_circ_266589,RMVar_hsa_circ_232195,RMVar_hsa_circ_68577,RMVar_hsa_circ_116406,RMVar_hsa_circ_24808,RMVar_hsa_circ_232198,RMVar_hsa_circ_127599,RMVar_hsa_circ_232200,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232206,RMVar_hsa_circ_232201,RMVar_hsa_circ_232202,RMVar_hsa_circ_344419,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_267014,RMVar_hsa_circ_232207,RMVar_hsa_circ_232204,RMVar_hsa_circ_232205,RMVar_hsa_circ_306242,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_30537,RMVar_hsa_circ_232213,RMVar_hsa_circ_232209,RMVar_hsa_circ_232211,RMVar_hsa_circ_232212,RMVar_hsa_circ_232210,RMVar_hsa_circ_363518,RMVar_hsa_circ_337416,RMVar_hsa_circ_356163,RMVar_hsa_circ_283938,RMVar_hsa_circ_232215,RMVar_hsa_circ_232217,RMVar_hsa_circ_232216,RMVar_hsa_circ_232214,RMVar_hsa_circ_232225,RMVar_hsa_circ_232221,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_120896,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232220,RMVar_hsa_circ_270747,RMVar_hsa_circ_332213,RMVar_hsa_circ_69265,RMVar_hsa_circ_232224 77286 RMVar_ID_77286 Human_SNP_ID_236202467 m1A Human chr5 + 71587493 71587493 71587493 TGCCCGCGCCTCTCCCGCCGGGCCGCGCGCCTATCACGGGGACTCGGTGGCCTCGCTGGGCACCC TGCCCGCGCCTCTCCCGCCGGGCCGCGCGCCTCTCACGGGGACTCGGTGGCCTCGCTGGGCACCC A C MCCC2 Ensembl:ENSG00000131844 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:71587391..71587500 26863410 MeRIP-seq:(Medium) rs1238687077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645542,Human_RBP_ID_4837811,Human_RBP_ID_5477077,Human_RBP_ID_8893548,Human_RBP_ID_9306460 Human_Splice_Rec_660567,Human_Splice_Rec_660585,Human_Splice_Rec_660611,Human_Splice_Rec_660629 77287 RMVar_ID_77287 Human_SNP_ID_236202468 m1A Human chr5 + 71587493 71587493 71587493 TGCCCGCGCCTCTCCCGCCGGGCCGCGCGCCTATCACGGGGACTCGGTGGCCTCGCTGGGCACCC TGCCCGCGCCTCTCCCGCCGGGCCGCGCGCCTGTCACGGGGACTCGGTGGCCTCGCTGGGCACCC A G MCCC2 Ensembl:ENSG00000131844 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:71587391..71587500 26863410 MeRIP-seq:(Medium) rs1238687077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645542,Human_RBP_ID_4837811,Human_RBP_ID_5477077,Human_RBP_ID_8893548,Human_RBP_ID_9306460 Human_Splice_Rec_660567,Human_Splice_Rec_660585,Human_Splice_Rec_660611,Human_Splice_Rec_660629 77288 RMVar_ID_77288 Human_SNP_ID_236202827 m1A Human chr5 + 71589013 71589013 71589013 ATGGTAGAATCATCAGTGTGGTGGCAATGTGGAGGATGGATTGATATAGGGAAAAGACTAGACCT ATGGTAGAATCATCAGTGTGGTGGCAATGTGGGGGATGGATTGATATAGGGAAAAGACTAGACCT A G MCCC2 Ensembl:ENSG00000131844 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:71589003..71589163 26863196 MeRIP-seq:(Medium) rs1395874752 Functional Loss SNV dbSNP153 33..33 33 - - - 77289 RMVar_ID_77289 Human_SNP_ID_236202839 m1A Human chr5 - 71589039 71589039 71589039 CAAGACTCAACTCTCCACTGTCACCTAGGTCTAGTCTTTTCCCTATATCAATCCATCCTCCACAT CAAGACTCAACTCTCCACTGTCACCTAGGTCTGGTCTTTTCCCTATATCAATCCATCCTCCACAT T C RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:71589036..71589164 26863196 MeRIP-seq:(Medium) rs994859934 Functional Loss SNV dbSNP153 33..33 33 - - - 77290 RMVar_ID_77290 Human_SNP_ID_236351412 m1A Human chr5 + 72195048 72195048 72195048 GCAAATCCGTGCGCAAGGAGTCAAAAGAAGAAACCCCTGAGGTCACAAAAGTGAATCACGTGGAA GCAAATCCGTGCGCAAGGAGTCAAAAGAAGAAGCCCCTGAGGTCACAAAAGTGAATCACGTGGAA A G MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:72195001..72195098 26863196 MeRIP-seq:(Medium) rs779582651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4837996,Human_RBP_ID_8891775,Human_RBP_ID_9179837,Human_RBP_ID_24548180,Human_RBP_ID_26352207 Human_miRNA_ID_3066895 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270,RMVar_hsa_circ_232277 77291 RMVar_ID_77291 Human_SNP_ID_236351543 m1A Human chr5 + 72195389 72195389 72195389 CCTATCAAGAAGGAGGAAAAACCAAAAAAGGAAGAGGTGAAAAAAGAAGTCAAAAAAGAGATCAA CCTATCAAGAAGGAGGAAAAACCAAAAAAGGAGGAGGTGAAAAAAGAAGTCAAAAAAGAGATCAA A G MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:72195339..72195544 26863196 MeRIP-seq:(Medium) rs756605010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4838013 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270,RMVar_hsa_circ_232277,RMVar_hsa_circ_232287 77292 RMVar_ID_77292 Human_SNP_ID_236351565 m1A Human chr5 + 72195445 72195445 72195445 AGAGATCAAGAAAGAAGAGAAAAAAGAACCCAAGAAAGAGGTTAAGAAAGAAACACCGCCAAAGG AGAGATCAAGAAAGAAGAGAAAAAAGAACCCAGGAAAGAGGTTAAGAAAGAAACACCGCCAAAGG A G MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:72195219..72195581;chr5:72195009..72195575;chr5:72195170..72195585 26863196 MeRIP-seq:(Medium) rs1561314162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9179842,Human_RBP_ID_24547955 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270,RMVar_hsa_circ_232277,RMVar_hsa_circ_232287 77293 RMVar_ID_77293 Human_SNP_ID_236351862 m1A Human chr5 - 72196301 72196301 72196301 ACAGACTCCCTCTTCTCCCTGATGTATGCATCAGCCTCCGCCTTGGCACTTTCCTCATCCTCAGT ACAGACTCCCTCTTCTCCCTGATGTATGCATCGGCCTCCGCCTTGGCACTTTCCTCATCCTCAGT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:72196262..72196408 26863196 MeRIP-seq:(Medium) rs1311954102 Functional Loss SNV dbSNP153 33..33 33 - - - 77294 RMVar_ID_77294 Human_SNP_ID_236351871 m1A Human chr5 - 72196329 72196329 72196329 TTCTTCGGCTCGGTCATCCCCACTGGCCACAGACTCCCTCTTCTCCCTGATGTATGCATCAGCCT TTCTTCGGCTCGGTCATCCCCACTGGCCACAGGCTCCCTCTTCTCCCTGATGTATGCATCAGCCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:72196196..72196345 26863196 MeRIP-seq:(Medium) rs1181012930 Functional Loss SNV dbSNP153 33..33 33 - - - 77295 RMVar_ID_77295 Human_SNP_ID_236351872 m1A Human chr5 - 72196329 72196329 72196329 TTCTTCGGCTCGGTCATCCCCACTGGCCACAGACTCCCTCTTCTCCCTGATGTATGCATCAGCCT TTCTTCGGCTCGGTCATCCCCACTGGCCACAGCCTCCCTCTTCTCCCTGATGTATGCATCAGCCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:72196196..72196345 26863196 MeRIP-seq:(Medium) rs1181012930 Functional Loss SNV dbSNP153 33..33 33 - - - 77296 RMVar_ID_77296 Human_SNP_ID_236351883 m1A Human chr5 - 72196366 72196366 72196366 GTTCAGCCTCTCCTTTCTCAATGGCCTCATCCATGTCTTCTTCGGCTCGGTCATCCCCACTGGCC GTTCAGCCTCTCCTTTCTCAATGGCCTCATCCGTGTCTTCTTCGGCTCGGTCATCCCCACTGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:72196273..72196484 26863196 MeRIP-seq:(Medium) rs757769805 Functional Loss SNV dbSNP153 33..33 33 - - - 77297 RMVar_ID_77297 Human_SNP_ID_236351905 m1A Human chr5 + 72196430 72196430 72196430 CAATCTGAAGAGGAGGCTGATGAGGAGGACAAAGCTGAAGATGCCAGAGAGGAGGAATATGAGCC CAATCTGAAGAGGAGGCTGATGAGGAGGACAAGGCTGAAGATGCCAGAGAGGAGGAATATGAGCC A G MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:72196258..72196461 26863196 MeRIP-seq:(Medium) rs571739603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214147,Human_RBP_ID_1660368,Human_RBP_ID_7465306,Human_RBP_ID_8891809,Human_RBP_ID_9262245,Human_RBP_ID_9306485,Human_RBP_ID_9397888,Human_RBP_ID_18413674,Human_RBP_ID_22099451,Human_RBP_ID_23116248,Human_RBP_ID_24548190,Human_RBP_ID_26350939,Human_RBP_ID_27574133,Human_RBP_ID_27825490 Human_miRNA_ID_957430,Human_miRNA_ID_2254367 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270,RMVar_hsa_circ_232277 77298 RMVar_ID_77298 Human_SNP_ID_236352999 m1A Human chr5 + 72199745 72199745 72199745 GAAAAGCCCCTCACTCAATCAGGGGGAGCCCCACCGCCTCCAGGAGGAAAGCAACAGGGCCGACA GAAAAGCCCCTCACTCAATCAGGGGGAGCCCCTCCGCCTCCAGGAGGAAAGCAACAGGGCCGACA A T MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:72199698..72199937 26863196 MeRIP-seq:(Medium) rs1193143021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7465330,Human_RBP_ID_8891940,Human_RBP_ID_17415214,Human_RBP_ID_18846532,Human_RBP_ID_22460078 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270 77299 RMVar_ID_77299 Human_SNP_ID_236354255 m1A Human chr5 - 72205547 72205547 72205547 CTCTCTCCCGCGCTCTCTCTCTCTCTAAGACAAATGCCTCTACCTAGCAGAAGTCAGTTGGGTTG CTCTCTCCCGCGCTCTCTCTCTCTCTAAGACAGATGCCTCTACCTAGCAGAAGTCAGTTGGGTTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72205496..72205602 32194978 MeRIP-seq:(Medium) rs779537912 Functional Loss SNV dbSNP153 33..33 33 - - - 77300 RMVar_ID_77300 Human_SNP_ID_236354287 m1A Human chr5 + 72205626 72205626 72205626 AGCACAAAGATAACGCAGGAGAGAGAGAGAGAAAGAATGAGAAAGAAAAGGAATGCAAGAGAAGG AGCACAAAGATAACGCAGGAGAGAGAGAGAGAGAGAATGAGAAAGAAAAGGAATGCAAGAGAAGG A G MAP1B Ensembl:ENSG00000131711 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:72205528..72205716;chr5:72205550..72205726;chr5:72205539..72205725 26863196 MeRIP-seq:(Medium) rs1305001296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4838268,Human_RBP_ID_5151279,Human_RBP_ID_7465341,Human_RBP_ID_24114780 RMVar_hsa_circ_94751,RMVar_hsa_circ_232270 77301 RMVar_ID_77301 Human_SNP_ID_236380604 m1A Human chr5 - 72320194 72320194 72320194 CCAAGATGGCTGCCTCCATAGTGCGGCGCGGGATGCTCCTGGCGCGGCAAGTGGTTCTTCCTCAG CCAAGATGGCTGCCTCCATAGTGCGGCGCGGGGTGCTCCTGGCGCGGCAAGTGGTTCTTCCTCAG T C MRPS27 Ensembl:ENSG00000113048 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72320126..72320200 32194978 MeRIP-seq:(Medium) rs1381098292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645725,Human_RBP_ID_4845770,Human_RBP_ID_15507397,Human_RBP_ID_18424964 Human_Splice_Rec_660769,Human_Splice_Rec_660813,Human_Splice_Rec_660891,Human_Splice_Rec_660901,Human_Splice_Rec_660909 77302 RMVar_ID_77302 Human_SNP_ID_236497603 m1A Human chr5 + 72827021 72827021 72827021 AGAAAATAAAGCAGTGAGAGGAAATGGAGAGTAAAGGGTAGGGTAGAGAGAAAAGGAAGAGGACA AGAAAATAAAGCAGTGAGAGGAAATGGAGAGTGAAGGGTAGGGTAGAGAGAAAAGGAAGAGGACA A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:72827015..72827112 26863196 MeRIP-seq:(Medium) rs1226973096 Functional Loss SNV dbSNP153 33..33 33 - - - 77303 RMVar_ID_77303 Human_SNP_ID_236502002 m1A Human chr5 - 72848213 72848202 72848214 GAGGTGCCCCGAAGGAAGTCACGGACAGTGAAACCCGGCGGAACTGCTCCTGGCAGCCCGGCCGC GAGGTGCCCCGAAGGAAGTCACGGACAGTGA____________CTGCTCCTGGCAGCCCGGCCGC GTTCCGCCGGGTT G RF00017-4501,lnc-ZNF366-12 RNACentral:URS0000972B66,RNACentral:URS00008BEDA5 SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:72848202..72848286 26863196 MeRIP-seq:(Medium) rs1308986280 Functional Loss DEL dbSNP153 32..43 33 - - - 77304 RMVar_ID_77304 Human_SNP_ID_236502014 m1A Human chr5 - 72848230 72848230 72848230 ACGCCGCGGACCTGCCTGAGGTGCCCCGAAGGAAGTCACGGACAGTGAAACCCGGCGGAACTGCT ACGCCGCGGACCTGCCTGAGGTGCCCCGAAGGGAGTCACGGACAGTGAAACCCGGCGGAACTGCT T C RF00017-4501,lnc-ZNF366-12 RNACentral:URS0000972B66,RNACentral:URS00008BEDA5 SRP RNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:72848225..72848416 26863196 MeRIP-seq:(Medium) rs894215289 Functional Loss SNV dbSNP153 33..33 33 - - - 77305 RMVar_ID_77305 Human_SNP_ID_236502022 m1A Human chr5 + 72848250 72848250 72848250 CTGTCCGTGACTTCCTTCGGGGCACCTCAGGCAGGTCCGCGGCGTTTGGGGAGCGCTGGGGTTGT CTGTCCGTGACTTCCTTCGGGGCACCTCAGGCCGGTCCGCGGCGTTTGGGGAGCGCTGGGGTTGT A C TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:72848245..72848345 32194978 MeRIP-seq:(Medium) rs1256339202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845772,Human_RBP_ID_9306514,Human_RBP_ID_18424965,Human_RBP_ID_19125733,Human_RBP_ID_26350951 Human_Splice_Rec_661297,Human_Splice_Rec_661305 RMVar_hsa_circ_232313 77306 RMVar_ID_77306 Human_SNP_ID_236502090 m1A Human chr5 + 72848386 72848386 72848386 CGTCTCTTCCTGTGTCTGGCTTTATTTGCAGCAAACCAAGATGGAGTATGAGTGGAAACCTGACG CGTCTCTTCCTGTGTCTGGCTTTATTTGCAGCCAACCAAGATGGAGTATGAGTGGAAACCTGACG A C TNPO1 Ensembl:ENSG00000083312 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72848376..72848500 32194978 MeRIP-seq:(Medium) rs1004062795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845773,Human_RBP_ID_9306515,Human_RBP_ID_9349858,Human_RBP_ID_9397891 Human_Splice_Rec_661176,Human_Splice_Rec_661226,Human_Splice_Rec_661232,Human_Splice_Rec_661248,Human_Splice_Rec_661292,Human_Splice_Rec_661298,Human_Splice_Rec_661306 RMVar_hsa_circ_113732,RMVar_hsa_circ_285989,RMVar_hsa_circ_351007,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_283268,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_232314 77307 RMVar_ID_77307 Human_SNP_ID_236518719 m1A Human chr5 + 72908948 72908946 72908949 AGTTACAACTCCGCAGTGGATGTGAAGAAGCAAAAAAAAAAAAATCTATTCAGTCTACTCACAAA AGTTACAACTCCGCAGTGGATGTGAAGAAGC___AAAAAAAAAATCTATTCAGTCTACTCACAAA CAAA C TNPO1 Ensembl:ENSG00000083312 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72908901..72909025 32194978 MeRIP-seq:(Medium) rs542484816 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_645779,Human_RBP_ID_8621512,Human_RBP_ID_17301170,Human_RBP_ID_17531214 Human_miRNA_ID_186011,Human_miRNA_ID_2004575 RMVar_hsa_circ_123423,RMVar_hsa_circ_232367 77308 RMVar_ID_77308 Human_SNP_ID_236518720 m1A Human chr5 + 72908948 72908946 72908949 AGTTACAACTCCGCAGTGGATGTGAAGAAGCAAAAAAAAAAAAATCTATTCAGTCTACTCACAAA AGTTACAACTCCGCAGTGGATGTGAAGAAGCA__AAAAAAAAAATCTATTCAGTCTACTCACAAA CAAA CA TNPO1 Ensembl:ENSG00000083312 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72908901..72909025 32194978 MeRIP-seq:(Medium) rs542484816 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_645779,Human_RBP_ID_8621512,Human_RBP_ID_17301170,Human_RBP_ID_17531214 Human_miRNA_ID_186011,Human_miRNA_ID_2004575 RMVar_hsa_circ_123423,RMVar_hsa_circ_232367 77309 RMVar_ID_77309 Human_SNP_ID_236647763 m1A Human chr5 - 73447055 73447055 73447055 CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCAGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCTGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA T A FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2972191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250552,Human_RBP_ID_1141481,Human_RBP_ID_5103333,Human_RBP_ID_8267815,Human_RBP_ID_17303586,Human_RBP_ID_17416990,Human_RBP_ID_17532539 Human_miRNA_ID_1829937,Human_miRNA_ID_1829972,Human_miRNA_ID_1853777,Human_miRNA_ID_1880419,Human_miRNA_ID_1909613 GWAS_ID_9250 77310 RMVar_ID_77310 Human_SNP_ID_236647764 m1A Human chr5 - 73447055 73447055 73447055 CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCAGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCGGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA T C FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2972191 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_250552,Human_RBP_ID_1141481,Human_RBP_ID_5103333,Human_RBP_ID_8267815,Human_RBP_ID_17303586,Human_RBP_ID_17416990,Human_RBP_ID_17532539 Human_miRNA_ID_1829937,Human_miRNA_ID_1829972,Human_miRNA_ID_1853777,Human_miRNA_ID_1880419,Human_miRNA_ID_1909613 GWAS_ID_9250 77311 RMVar_ID_77311 Human_SNP_ID_236648012 m1A Human chr5 - 73447551 73447536 73447551 CGCGCCCCCGCCGCCCCCGCATGCCTACGGCTACGGCCCCTACGGCTGCGGCTACGGCCTGCAGC CGCGCCCCCGCCGCCCCCGCATGCCTACGGCT_______________GCGGCTACGGCCTGCAGC CAGCCGTAGGGGCCGT C FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:73447489..73447589 26863410 MeRIP-seq:(Medium) rs1488844616 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_645982,Human_RBP_ID_5103334,Human_RBP_ID_5267659,Human_RBP_ID_21990521 77312 RMVar_ID_77312 Human_SNP_ID_236648016 m1A Human chr5 - 73447551 73447551 73447551 CGCGCCCCCGCCGCCCCCGCATGCCTACGGCTACGGCCCCTACGGCTGCGGCTACGGCCTGCAGC CGCGCCCCCGCCGCCCCCGCATGCCTACGGCTTCGGCCCCTACGGCTGCGGCTACGGCCTGCAGC T A FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:73447489..73447589 26863410 MeRIP-seq:(Medium) rs1014204417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645982,Human_RBP_ID_5103334,Human_RBP_ID_5267659,Human_RBP_ID_21990521 77313 RMVar_ID_77313 Human_SNP_ID_236648040 m1A Human chr5 - 73447628 73447601 73447628 GAGTCTCTGCTGCTGCGCGGCGCGGGAGCCGCAGGGGGCGCGGGCGACCCGGCAGCCGCCGCCGC GAGTCTCTGCTGCTGCGCGGCGCGGGAGCCGC___________________________CGCCGC GGCGGCTGCCGGGTCGCCCGCGCCCCCT G FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:73447526..73447700 26863410 MeRIP-seq:(Medium) rs1299800082 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_645983 77314 RMVar_ID_77314 Human_SNP_ID_236648054 m1A Human chr5 - 73447628 73447628 73447628 GAGTCTCTGCTGCTGCGCGGCGCGGGAGCCGCAGGGGGCGCGGGCGACCCGGCAGCCGCCGCCGC GAGTCTCTGCTGCTGCGCGGCGCGGGAGCCGCTGGGGGCGCGGGCGACCCGGCAGCCGCCGCCGC T A FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:73447526..73447700 26863410 MeRIP-seq:(Medium) rs1222362473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645983 77315 RMVar_ID_77315 Human_SNP_ID_236648184 m1A Human chr5 + 73447958 73447958 73447958 AGCCGCTTCTTGGGGCTCTGCAGGATGGCCATAGTGATGAGCGCGATATACGAGTAGGGCGGCTT AGCCGCTTCTTGGGGCTCTGCAGGATGGCCATGGTGATGAGCGCGATATACGAGTAGGGCGGCTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:73447687..73447984 32194978 MeRIP-seq:(Medium) rs1268732268 Functional Loss SNV dbSNP153 33..33 33 - - - 77316 RMVar_ID_77316 Human_SNP_ID_236660405 m1A Human chr5 - 73499087 73499087 73499087 AATCCTCAGCAAGGATAGGTTTAGCTCACTCTAGCATTCCATGCTCGTTATTTCCCAAGATACCA AATCCTCAGCAAGGATAGGTTTAGCTCACTCTGGCATTCCATGCTCGTTATTTCCCAAGATACCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:73499083..73499237 26863196 MeRIP-seq:(Medium) rs773267383 Functional Loss SNV dbSNP153 33..33 33 - - - 77317 RMVar_ID_77317 Human_SNP_ID_236661321 m1A Human chr5 - 73502442 73502442 73502442 GAAGAGGAAAGAAAACAGCACATTTATACCACAACAGATATTTTTCAAATGGGAATAGTTTCCAA GAAGAGGAAAGAAAACAGCACATTTATACCACCACAGATATTTTTCAAATGGGAATAGTTTCCAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:73502439..73502575 26863196 MeRIP-seq:(Medium) rs370907547 Functional Loss SNV dbSNP153 33..33 33 - - - 77318 RMVar_ID_77318 Human_SNP_ID_236661495 m1A Human chr5 - 73503061 73503039 73503061 GTCTCCTTAAACTAGTCAGACTATCCGCACCAAGCTGGTTTAAGATGCTGGGTAGCATTTCTGTC GTCTCCTTAAACTAGTCAGACTATCCGCACCA______________________GCATTTCTGTC CTACCCAGCATCTTAAACCAGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:73502953..73503139 26863196 MeRIP-seq:(Medium) rs1190998330 Functional Loss DEL dbSNP153 33..54 33 - - - 77319 RMVar_ID_77319 Human_SNP_ID_236661499 m1A Human chr5 - 73503061 73503061 73503061 GTCTCCTTAAACTAGTCAGACTATCCGCACCAAGCTGGTTTAAGATGCTGGGTAGCATTTCTGTC GTCTCCTTAAACTAGTCAGACTATCCGCACCAGGCTGGTTTAAGATGCTGGGTAGCATTTCTGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:73502953..73503139 26863196 MeRIP-seq:(Medium) rs1282265190 Functional Loss SNV dbSNP153 33..33 33 - - - 77320 RMVar_ID_77320 Human_SNP_ID_236662104 m1A Human chr5 - 73505266 73505266 73505266 AATATAAAATAGCAGCTCCCAGTAACTTCTTCAGGTTTTATCTTCAGAAGTTGACTCAATTCAGT AATATAAAATAGCAGCTCCCAGTAACTTCTTCCGGTTTTATCTTCAGAAGTTGACTCAATTCAGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:73505176..73505325 32194978 MeRIP-seq:(Medium) rs1561255553 Functional Loss SNV dbSNP153 33..33 33 - - - 77321 RMVar_ID_77321 Human_SNP_ID_236676887 m1A Human chr5 - 73565531 73565531 73565531 CGGAGCGTAAAGGCGGCAAAAACAAAAATATTAAAAAAAAGGAGAGAGGGACAAAAAAAAGAAAA CGGAGCGTAAAGGCGGCAAAAACAAAAATATTTAAAAAAAGGAGAGAGGGACAAAAAAAAGAAAA T A ANKRA2 Ensembl:ENSG00000164331 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:73565480..73565625 26863196 MeRIP-seq:(Medium) rs531091267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4856881,Human_RBP_ID_5509886,Human_RBP_ID_27517204 77322 RMVar_ID_77322 Human_SNP_ID_236753230 m1A Human chr5 + 73895277 73895277 73895277 ATGGTGGCCGAGGTTGGGTGAAGGGCAAGGTCATTGGAGATGAGAAAGTCCAGAGGATGAGAGGC ATGGTGGCCGAGGTTGGGTGAAGGGCAAGGTCGTTGGAGATGAGAAAGTCCAGAGGATGAGAGGC A G ARHGEF28 Ensembl:ENSG00000214944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:73895123..73895356 26863196 MeRIP-seq:(Medium) rs764893201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839277 RMVar_hsa_circ_59719,RMVar_hsa_circ_3955,RMVar_hsa_circ_333457,RMVar_hsa_circ_62629,RMVar_hsa_circ_75839,RMVar_hsa_circ_232457,RMVar_hsa_circ_68684,RMVar_hsa_circ_268434,RMVar_hsa_circ_328521,RMVar_hsa_circ_350118,RMVar_hsa_circ_232460,RMVar_hsa_circ_355327 77323 RMVar_ID_77323 Human_SNP_ID_236756632 m1A Human chr5 + 73909725 73909725 73909725 GCAGGAGGAGCTGCTGCTGCGGAGCCGGGGCGAGCTGGACCTCCAGCTCCAGGAGTACCAGCACA GCAGGAGGAGCTGCTGCTGCGGAGCCGGGGCGGGCTGGACCTCCAGCTCCAGGAGTACCAGCACA A G ARHGEF28 Ensembl:ENSG00000214944 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:73909675..73909773 26863196 MeRIP-seq:(Medium) rs1010379855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944342,Human_RBP_ID_23050346,Human_RBP_ID_23120192 RMVar_hsa_circ_59719,RMVar_hsa_circ_333457,RMVar_hsa_circ_62629,RMVar_hsa_circ_68684,RMVar_hsa_circ_268434,RMVar_hsa_circ_328521,RMVar_hsa_circ_232460,RMVar_hsa_circ_22289,RMVar_hsa_circ_70122,RMVar_hsa_circ_317027,RMVar_hsa_circ_366322 77324 RMVar_ID_77324 Human_SNP_ID_236947903 m1A Human chr5 - 74685376 74685376 74685376 CCGAGACGCTCGGGGCCCGAGCCGCCTCCGCCACCTGCACCACCAGCGCCACCTGAGTCAGCAGC CCGAGACGCTCGGGGCCCGAGCCGCCTCCGCCGCCTGCACCACCAGCGCCACCTGAGTCAGCAGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:74685326..74685575 32194978 MeRIP-seq:(Medium) rs1412468393 Functional Loss SNV dbSNP153 33..33 33 - - - 77325 RMVar_ID_77325 Human_SNP_ID_236947936 m1A Human chr5 - 74685427 74685427 74685427 GGGTCATCTTCACCAAGAGCGGCAGGGGCCACAGCGCCGGCCCCGGCTTGGCCGAGACGCTCGGG GGGTCATCTTCACCAAGAGCGGCAGGGGCCACTGCGCCGGCCCCGGCTTGGCCGAGACGCTCGGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:74640519..74685475 26863410 MeRIP-seq:(Medium) rs368384256 Functional Loss SNV dbSNP153 33..33 33 - - - 77326 RMVar_ID_77326 Human_SNP_ID_236947987 m1A Human chr5 + 74685511 74685511 74685511 CCCGGAGAACTTCTACATCAGCCACAGCCCCAATTCCACGGCGGGCCCCTCCTGCACCCTGCTGG CCCGGAGAACTTCTACATCAGCCACAGCCCCAGTTCCACGGCGGGCCCCTCCTGCACCCTGCTGG A G HEXB Ensembl:ENSG00000049860 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:74685501..74685525 26863196 MeRIP-seq:(Medium) rs200209801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249757,Human_RBP_ID_787365,Human_RBP_ID_17415233,Human_RBP_ID_22771910,Human_RBP_ID_27517236 Human_Splice_Rec_662475,Human_Splice_Rec_662485,Human_Splice_Rec_662487 Human_miRNA_ID_2389753,Human_miRNA_ID_2590979 RMVar_hsa_circ_83779,RMVar_hsa_circ_105350,RMVar_hsa_circ_232469,RMVar_hsa_circ_232470 77327 RMVar_ID_77327 Human_SNP_ID_236947988 m1A Human chr5 + 74685511 74685511 74685511 CCCGGAGAACTTCTACATCAGCCACAGCCCCAATTCCACGGCGGGCCCCTCCTGCACCCTGCTGG CCCGGAGAACTTCTACATCAGCCACAGCCCCATTTCCACGGCGGGCCCCTCCTGCACCCTGCTGG A T HEXB Ensembl:ENSG00000049860 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:74685501..74685525 26863196 MeRIP-seq:(Medium) rs200209801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249757,Human_RBP_ID_787365,Human_RBP_ID_17415233,Human_RBP_ID_22771910,Human_RBP_ID_27517236 Human_Splice_Rec_662475,Human_Splice_Rec_662485,Human_Splice_Rec_662487 Human_miRNA_ID_2389753,Human_miRNA_ID_2590979 RMVar_hsa_circ_83779,RMVar_hsa_circ_105350,RMVar_hsa_circ_232469,RMVar_hsa_circ_232470 77328 RMVar_ID_77328 Human_SNP_ID_236966473 m1A Human chr5 - 74759384 74759384 74759384 AAATGATATCAAATCCCTTCATTCCATCATCAATCCTCCCATAGCTAAGTAAGTACTATCATTAT AAATGATATCAAATCCCTTCATTCCATCATCATTCCTCCCATAGCTAAGTAAGTACTATCATTAT T A GFM2 Ensembl:ENSG00000164347 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs957680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17531319,Human_RBP_ID_18052644 Human_Splice_Rec_662580,Human_Splice_Rec_662581,Human_Splice_Rec_662620,Human_Splice_Rec_662621,Human_Splice_Rec_662660,Human_Splice_Rec_662661,Human_Splice_Rec_662722,Human_Splice_Rec_662723,Human_Splice_Rec_662752,Human_Splice_Rec_662753,Human_Splice_Rec_662770,Human_Splice_Rec_662771 GWAS_ID_9251,GWAS_ID_9252,GWAS_ID_9253,GWAS_ID_9254,GWAS_ID_9255,GWAS_ID_9256,GWAS_ID_9257,GWAS_ID_9258,GWAS_ID_9259,GWAS_ID_9260,GWAS_ID_9261,GWAS_ID_9262,GWAS_ID_9263 RMVar_hsa_circ_74241,RMVar_hsa_circ_101228,RMVar_hsa_circ_232484,RMVar_hsa_circ_69638,RMVar_hsa_circ_330693,RMVar_hsa_circ_312595 77329 RMVar_ID_77329 Human_SNP_ID_236966474 m1A Human chr5 - 74759384 74759384 74759384 AAATGATATCAAATCCCTTCATTCCATCATCAATCCTCCCATAGCTAAGTAAGTACTATCATTAT AAATGATATCAAATCCCTTCATTCCATCATCAGTCCTCCCATAGCTAAGTAAGTACTATCATTAT T C GFM2 Ensembl:ENSG00000164347 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs957680 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17531319,Human_RBP_ID_18052644 Human_Splice_Rec_662580,Human_Splice_Rec_662581,Human_Splice_Rec_662620,Human_Splice_Rec_662621,Human_Splice_Rec_662660,Human_Splice_Rec_662661,Human_Splice_Rec_662722,Human_Splice_Rec_662723,Human_Splice_Rec_662752,Human_Splice_Rec_662753,Human_Splice_Rec_662770,Human_Splice_Rec_662771 GWAS_ID_9251,GWAS_ID_9252,GWAS_ID_9253,GWAS_ID_9254,GWAS_ID_9255,GWAS_ID_9256,GWAS_ID_9257,GWAS_ID_9258,GWAS_ID_9259,GWAS_ID_9260,GWAS_ID_9261,GWAS_ID_9262,GWAS_ID_9263 RMVar_hsa_circ_74241,RMVar_hsa_circ_101228,RMVar_hsa_circ_232484,RMVar_hsa_circ_69638,RMVar_hsa_circ_330693,RMVar_hsa_circ_312595 77330 RMVar_ID_77330 Human_SNP_ID_236968440 m1A Human chr5 - 74767339 74767339 74767339 CTCCTTACCATGGTGACGGCCGCAGAGCCGCCAGGAGCAGCCGCTGGAGTGCGAAAACGCTCTCA CTCCTTACCATGGTGACGGCCGCAGAGCCGCCCGGAGCAGCCGCTGGAGTGCGAAAACGCTCTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:74767288..74767401 26863196 MeRIP-seq:(Medium) rs759771167 Functional Loss SNV dbSNP153 33..33 33 - - - 77331 RMVar_ID_77331 Human_SNP_ID_236971993 m1A Human chr5 - 74780385 74780385 74780385 TCCAATCAACAGATCTTCCTGCCTGCCGGCTTATGCCCTTGATGTCCATTTTTGGGTAGGTTTGG TCCAATCAACAGATCTTCCTGCCTGCCGGCTTGTGCCCTTGATGTCCATTTTTGGGTAGGTTTGG T C FAM169A Ensembl:ENSG00000198780 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3733794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4839314,Human_RBP_ID_17303385,Human_RBP_ID_17532189,Human_RBP_ID_27743762 Human_miRNA_ID_646369,Human_miRNA_ID_1373647 GWAS_ID_9264,GWAS_ID_9265,GWAS_ID_9266,GWAS_ID_9267,GWAS_ID_9268,GWAS_ID_9269,GWAS_ID_9270,GWAS_ID_9271,GWAS_ID_9272,GWAS_ID_9273,GWAS_ID_9274,GWAS_ID_9275,GWAS_ID_9276,GWAS_ID_9277,GWAS_ID_9278,GWAS_ID_9279,GWAS_ID_9280,GWAS_ID_9281,GWAS_ID_9282,GWAS_ID_9283,GWAS_ID_9284,GWAS_ID_9285,GWAS_ID_9286,GWAS_ID_9287,GWAS_ID_9288,GWAS_ID_9289,GWAS_ID_9290,GWAS_ID_9291,GWAS_ID_9292,GWAS_ID_9293 RMVar_hsa_circ_232493 77332 RMVar_ID_77332 Human_SNP_ID_236993497 m1A Human chr5 + 74866405 74866405 74866405 ACGACGTGACGCACTAGCGCCGCAGCGCCTCCAGCCTTCGCTTCCGCTCCGCGCCCGCGCCCACC ACGACGTGACGCACTAGCGCCGCAGCGCCTCCCGCCTTCGCTTCCGCTCCGCGCCCGCGCCCACC A C AC010501.2 Ensembl:ENSG00000271714 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:74866242..74866610 26863196 MeRIP-seq:(Medium) rs1561334711 Functional Loss SNV dbSNP153 33..33 33 - - - 77333 RMVar_ID_77333 Human_SNP_ID_236993501 m1A Human chr5 - 74866415 74866415 74866415 GGGGATTCGCGGTGGGCGCGGGCGCGGAGCGGAAGCGAAGGCTGGAGGCGCTGCGGCGCTAGTGC GGGGATTCGCGGTGGGCGCGGGCGCGGAGCGGCAGCGAAGGCTGGAGGCGCTGCGGCGCTAGTGC T G FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:74866284..74866530 26863196 MeRIP-seq:(Medium) rs1361140438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840057,Human_RBP_ID_3783271,Human_RBP_ID_4839380,Human_RBP_ID_5213809,Human_RBP_ID_5242489,Human_RBP_ID_8730183,Human_RBP_ID_9436536,Human_RBP_ID_18425121,Human_RBP_ID_22418592,Human_RBP_ID_22702593,Human_RBP_ID_26791932 RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 77334 RMVar_ID_77334 Human_SNP_ID_236993523 m1A Human chr5 - 74866484 74866484 74866484 GCCGGGGCTGGAGGGAGGCAGGGCGGCGTCCCAGGCTCCGAGGAGGGGCCGCTCCGCGCTGGCGG GCCGGGGCTGGAGGGAGGCAGGGCGGCGTCCCTGGCTCCGAGGAGGGGCCGCTCCGCGCTGGCGG T A FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:74866228..74866802 26863196 MeRIP-seq:(Medium) rs1286146180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783272,Human_RBP_ID_5397289,Human_RBP_ID_9436536,Human_RBP_ID_26792082 RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 77335 RMVar_ID_77335 Human_SNP_ID_236993524 m1A Human chr5 - 74866484 74866484 74866484 GCCGGGGCTGGAGGGAGGCAGGGCGGCGTCCCAGGCTCCGAGGAGGGGCCGCTCCGCGCTGGCGG GCCGGGGCTGGAGGGAGGCAGGGCGGCGTCCCGGGCTCCGAGGAGGGGCCGCTCCGCGCTGGCGG T C FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:74866228..74866802 26863196 MeRIP-seq:(Medium) rs1286146180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783272,Human_RBP_ID_5397289,Human_RBP_ID_9436536,Human_RBP_ID_26792082 RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 77336 RMVar_ID_77336 Human_SNP_ID_193654474 m1A Human chr4 - 90127559 90127559 90127559 TTGAGACAGAGAGAGAGAGAGAGGAGAGGCGGATTGGCAGTAGGTCGGCGACTATTTGTGGTGAG TTGAGACAGAGAGAGAGAGAGAGGAGAGGCGGCTTGGCAGTAGGTCGGCGACTATTTGTGGTGAG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:90127463..90127576 26863196 MeRIP-seq:(Medium) rs530635243 Functional Loss SNV dbSNP153 33..33 33 - - - 77337 RMVar_ID_77337 Human_SNP_ID_193654505 m1A Human chr4 + 90127651 90127642 90127651 GGCAGAGCAGCTCCGCTGGCGCAGGCAGGAGGAGCAGGAGGATTATTAAATAACGCAGCTGGACT GGCAGAGCAGCTCCGCTGGCGCAG_________GCAGGAGGATTATTAAATAACGCAGCTGGACT GGCAGGAGGA G CCSER1 Ensembl:ENSG00000184305 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:90127602..90127764 26863196 MeRIP-seq:(Medium) rs1321139991 Functional Loss DEL dbSNP153 25..33 33 - - - 77338 RMVar_ID_77338 Human_SNP_ID_193714905 m1A Human chr4 + 90369272 90369267 90369273 AGGACAAAGATGAGGATGAGGAGGAAGAAAGAAGAAGAAGAAAGAAAGGAGGAGGAAAAGAAGAA AGGACAAAGATGAGGATGAGGAGGAAGA______AAGAAGAAAGAAAGGAGGAGGAAAAGAAGAA AAAGAAG A CCSER1 Ensembl:ENSG00000184305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:90369242..90369350 26863196 MeRIP-seq:(Medium) rs140388423 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_49553,RMVar_hsa_circ_281363,RMVar_hsa_circ_315450,RMVar_hsa_circ_331540,RMVar_hsa_circ_48653,RMVar_hsa_circ_227479 77339 RMVar_ID_77339 Human_SNP_ID_193714906 m1A Human chr4 + 90369272 90369267 90369273 AGGACAAAGATGAGGATGAGGAGGAAGAAAGAAGAAGAAGAAAGAAAGGAGGAGGAAAAGAAGAA AGGACAAAGATGAGGATGAGGAGGAAGAAAG___AAGAAGAAAGAAAGGAGGAGGAAAAGAAGAA AAAGAAG AAAG CCSER1 Ensembl:ENSG00000184305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:90369242..90369350 26863196 MeRIP-seq:(Medium) rs140388423 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_49553,RMVar_hsa_circ_281363,RMVar_hsa_circ_315450,RMVar_hsa_circ_331540,RMVar_hsa_circ_48653,RMVar_hsa_circ_227479 77340 RMVar_ID_77340 Human_SNP_ID_194614593 m1A Human chr4 + 93829272 93829272 93829272 TGGTAAGGAGGAGCAGCGGCGGTGCCAGCAGCAGCAAGAGCCCCGGGCCGGTGAAAGTGCGGGAA TGGTAAGGAGGAGCAGCGGCGGTGCCAGCAGCGGCAAGAGCCCCGGGCCGGTGAAAGTGCGGGAA A G ATOH1 Ensembl:ENSG00000172238 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:93829194..93829293 26863196 MeRIP-seq:(Medium) rs1455550700 Functional Loss SNV dbSNP153 33..33 33 - - - 77341 RMVar_ID_77341 Human_SNP_ID_194692113 m1A Human chr4 + 94147261 94147261 94147261 CTTCTTGCTTTATTTCATTAATTTGATCTTCAATCACTGAAACCCTTTCTTCTACTTGATCGAAT CTTCTTGCTTTATTTCATTAATTTGATCTTCAGTCACTGAAACCCTTTCTTCTACTTGATCGAAT A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:94147177..94147279 26863410 MeRIP-seq:(Medium) rs1038998864 Functional Loss SNV dbSNP153 33..33 33 - - - 77342 RMVar_ID_77342 Human_SNP_ID_194712301 m1A Human chr4 - 94227540 94227540 94227540 TTTATCTCCCAACCCACATGAAATCCAGCAACAAATCCTCTCTTGCTCCATCTTCAAAGTATATT TTTATCTCCCAACCCACATGAAATCCAGCAACGAATCCTCTCTTGCTCCATCTTCAAAGTATATT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:94227490..94227622 26863196 MeRIP-seq:(Medium) rs887772456 Functional Loss SNV dbSNP153 33..33 33 - - - 77343 RMVar_ID_77343 Human_SNP_ID_194770049 m1A Human chr4 + 94451994 94451994 94451994 GGCGGAGGCAGCCCCGCGCCGCGCCGGACCCGAGGTGAGTGGCGGCCGGCCGGCGATGCGCCTCT GGCGGAGGCAGCCCCGCGCCGCGCCGGACCCGGGGTGAGTGGCGGCCGGCCGGCGATGCGCCTCT A G PDLIM5 Ensembl:ENSG00000163110 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:94451973..94452250 26863196 MeRIP-seq:(Medium) rs1418629697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837923,Human_RBP_ID_4795057,Human_RBP_ID_17409304,Human_RBP_ID_18424787,Human_RBP_ID_22095954,Human_RBP_ID_24561763 Human_Splice_Rec_583819,Human_Splice_Rec_583837,Human_Splice_Rec_583853,Human_Splice_Rec_583875,Human_Splice_Rec_583907,Human_Splice_Rec_583911,Human_Splice_Rec_583921,Human_Splice_Rec_583923,Human_Splice_Rec_583929,Human_Splice_Rec_583957,Human_Splice_Rec_583961,Human_Splice_Rec_583985,Human_Splice_Rec_584007 RMVar_hsa_circ_84692,RMVar_hsa_circ_227547 77344 RMVar_ID_77344 Human_SNP_ID_194842116 m1A Human chr4 + 94758042 94758042 94758042 CGCCGGGCAGTGCGGAGACCGCGGCGCTGAGGACGCGGGAGCCGGGAGCGCAGCCGCGGGTAAGG CGCCGGGCAGTGCGGAGACCGCGGCGCTGAGGCCGCGGGAGCCGGGAGCGCAGCCGCGGGTAAGG A C BMPR1B Ensembl:ENSG00000138696 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:94757859..94758288 26863196 MeRIP-seq:(Medium) rs1336917072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_584151 77345 RMVar_ID_77345 Human_SNP_ID_194872632 m1A Human chr4 - 94875784 94875782 94875784 ACAAAAACTGAATTGCTATTTGTGGCTTGAGAAAGGTTTATTATTATTTACCAGTTCAAATGCAG ACAAAAACTGAATTGCTATTTGTGGCTTGAGA__GGTTTATTATTATTTACCAGTTCAAATGCAG CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:94875779..94875898 26863196 MeRIP-seq:(Medium) rs1180356923 Functional Loss DEL dbSNP153 33..34 33 - - - 77346 RMVar_ID_77346 Human_SNP_ID_194872635 m1A Human chr4 - 94875784 94875784 94875784 ACAAAAACTGAATTGCTATTTGTGGCTTGAGAAAGGTTTATTATTATTTACCAGTTCAAATGCAG ACAAAAACTGAATTGCTATTTGTGGCTTGAGATAGGTTTATTATTATTTACCAGTTCAAATGCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:94875779..94875898 26863196 MeRIP-seq:(Medium) rs1174470576 Functional Loss SNV dbSNP153 33..33 33 - - - 77347 RMVar_ID_77347 Human_SNP_ID_195729752 m1A Human chr4 + 98261499 98261499 98261499 CTGCGGGAGAGACGGAGGTAGAGGGAGGACACAGAGCCGCGCCGCCCGCACCACAGACCTTCGCC CTGCGGGAGAGACGGAGGTAGAGGGAGGACACGGAGCCGCGCCGCCCGCACCACAGACCTTCGCC A G RAP1GDS1 Ensembl:ENSG00000138698 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:98261393..98261536 26863196 MeRIP-seq:(Medium) rs1315138807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795059 Human_Splice_Rec_584521,Human_Splice_Rec_584527,Human_Splice_Rec_584555,Human_Splice_Rec_584563,Human_Splice_Rec_584589,Human_Splice_Rec_584597,Human_Splice_Rec_584621,Human_Splice_Rec_584631,Human_Splice_Rec_584639,Human_Splice_Rec_584649,Human_Splice_Rec_584657,Human_Splice_Rec_584665,Human_Splice_Rec_584693,Human_Splice_Rec_584699,Human_Splice_Rec_584707,Human_Splice_Rec_584715,Human_Splice_Rec_584725,Human_Splice_Rec_584751 77348 RMVar_ID_77348 Human_SNP_ID_195774481 m1A Human chr4 - 98442167 98442167 98442167 TAGAGAATGAAGCGGAAGAAGCCGCTGGATGGAGGACAGAGGGGAAATTAGAGATGGGATGATGC TAGAGAATGAAGCGGAAGAAGCCGCTGGATGGGGGACAGAGGGGAAATTAGAGATGGGATGATGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:98442116..98442198 32194978 MeRIP-seq:(Medium) rs1045508758 Functional Loss SNV dbSNP153 33..33 33 - - - 77349 RMVar_ID_77349 Human_SNP_ID_195880751 m1A Human chr4 + 98901929 98901929 98901929 ATATAGTGTTCTGGGTTAGCAACCTCCTGATTAGATTCCGTTTTCTCCTCTTCTGTAGTCGGGGG ATATAGTGTTCTGGGTTAGCAACCTCCTGATTGGATTCCGTTTTCTCCTCTTCTGTAGTCGGGGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:98901891..98902019 26863196 MeRIP-seq:(Medium) rs559148220 Functional Loss SNV dbSNP153 33..33 33 - - - 77350 RMVar_ID_77350 Human_SNP_ID_195880757 m1A Human chr4 - 98901950 98901950 98901950 GAAACCACCCCTACTCCTAATCCCCCGACTACAGAAGAGGAGAAAACGGAATCTAATCAGGAGGT GAAACCACCCCTACTCCTAATCCCCCGACTACTGAAGAGGAGAAAACGGAATCTAATCAGGAGGT T A EIF4E Ensembl:ENSG00000151247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:98901901..98902000;chr4:98901839..98901978;chr4:98901847..98902023;chr4:98901880..98902027 26863196 MeRIP-seq:(Medium) rs538537081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1641541,Human_RBP_ID_4794375,Human_RBP_ID_5210569,Human_RBP_ID_7342193,Human_RBP_ID_17409308,Human_RBP_ID_26349471 Human_Splice_Rec_584906,Human_Splice_Rec_584907,Human_Splice_Rec_584918,Human_Splice_Rec_584919,Human_Splice_Rec_584930,Human_Splice_Rec_584931,Human_Splice_Rec_584938,Human_Splice_Rec_584939,Human_Splice_Rec_584950,Human_Splice_Rec_584951,Human_Splice_Rec_584962,Human_Splice_Rec_584963,Human_Splice_Rec_584982,Human_Splice_Rec_584983,Human_Splice_Rec_584994,Human_Splice_Rec_584995 RMVar_hsa_circ_35056,RMVar_hsa_circ_39129,RMVar_hsa_circ_29622,RMVar_hsa_circ_41106 77351 RMVar_ID_77351 Human_SNP_ID_195880758 m1A Human chr4 - 98901950 98901950 98901950 GAAACCACCCCTACTCCTAATCCCCCGACTACAGAAGAGGAGAAAACGGAATCTAATCAGGAGGT GAAACCACCCCTACTCCTAATCCCCCGACTACGGAAGAGGAGAAAACGGAATCTAATCAGGAGGT T C EIF4E Ensembl:ENSG00000151247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:98901901..98902000;chr4:98901839..98901978;chr4:98901847..98902023;chr4:98901880..98902027 26863196 MeRIP-seq:(Medium) rs538537081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1641541,Human_RBP_ID_4794375,Human_RBP_ID_5210569,Human_RBP_ID_7342193,Human_RBP_ID_17409308,Human_RBP_ID_26349471 Human_Splice_Rec_584906,Human_Splice_Rec_584907,Human_Splice_Rec_584918,Human_Splice_Rec_584919,Human_Splice_Rec_584930,Human_Splice_Rec_584931,Human_Splice_Rec_584938,Human_Splice_Rec_584939,Human_Splice_Rec_584950,Human_Splice_Rec_584951,Human_Splice_Rec_584962,Human_Splice_Rec_584963,Human_Splice_Rec_584982,Human_Splice_Rec_584983,Human_Splice_Rec_584994,Human_Splice_Rec_584995 RMVar_hsa_circ_35056,RMVar_hsa_circ_39129,RMVar_hsa_circ_29622,RMVar_hsa_circ_41106 77352 RMVar_ID_77352 Human_SNP_ID_195882520 m1A Human chr4 - 98909744 98909744 98909744 AAAAAGAAGCAAAACAAGAAGGAAAGAAAAAAAATGAGAGCTGAAGATGGTGAAAATGATGCCAT AAAAAGAAGCAAAACAAGAAGGAAAGAAAAAACATGAGAGCTGAAGATGGTGAAAATGATGCCAT T G TBCAP3,EIF4E Ensembl:ENSG00000249055,Ensembl:ENSG00000151247 Pseudogene,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:98909742..98909947 26863196 MeRIP-seq:(Medium) rs750008773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3750264,Human_RBP_ID_5102856,Human_RBP_ID_17409533,Human_RBP_ID_18537494 Human_Splice_Rec_584949 RMVar_hsa_circ_29622 77353 RMVar_ID_77353 Human_SNP_ID_195887792 m1A Human chr4 - 98928859 98928859 98928859 GGGGCCCGAGAACTGGGGGAGCGGTGTGGGGGAGGGGCGGCGTGGCGCCTCCTGCGGAACCGCGA GGGGCCCGAGAACTGGGGGAGCGGTGTGGGGGGGGGGCGGCGTGGCGCCTCCTGCGGAACCGCGA T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:98928855..98929124 26863196 MeRIP-seq:(Medium) rs1481019188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249469,Human_RBP_ID_3748222,Human_RBP_ID_5242127,Human_RBP_ID_5394396,Human_RBP_ID_8211771,Human_RBP_ID_9435823,Human_RBP_ID_26791636 77354 RMVar_ID_77354 Human_SNP_ID_195887872 m1A Human chr4 - 98929019 98929019 98929019 CCGTCTTCCTTCTGACTGGGGGACTCCGCGGGACGGCGTTCCCGGCGCGCACTGTACCCCTTGCC CCGTCTTCCTTCTGACTGGGGGACTCCGCGGGGCGGCGTTCCCGGCGCGCACTGTACCCCTTGCC T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:98929016..98929107 26863410 MeRIP-seq:(Medium) rs934527224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786811,Human_RBP_ID_18501012,Human_RBP_ID_19121744,Human_RBP_ID_24431015 77355 RMVar_ID_77355 Human_SNP_ID_195917109 m1A Human chr4 - 99052422 99052422 99052422 TCCCTGAGGCCTCTCCAGAAGCTGATGCTGCCATGCTTGTATAGCCTGCAGAACCGTGAGCCAAT TCCCTGAGGCCTCTCCAGAAGCTGATGCTGCCGTGCTTGTATAGCCTGCAGAACCGTGAGCCAAT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:99052374..99052531 26863196 MeRIP-seq:(Medium) rs1183674073 Functional Loss SNV dbSNP153 33..33 33 - - - 77356 RMVar_ID_77356 Human_SNP_ID_195919435 m1A Human chr4 + 99062432 99062432 99062432 GGAACCTCATTAGAAATGACCTCAGCTGCCCCATATCTACGTTCCTTTCAGCAGTTGTCCAAGTA GGAACCTCATTAGAAATGACCTCAGCTGCCCCGTATCTACGTTCCTTTCAGCAGTTGTCCAAGTA A G METAP1 Ensembl:ENSG00000164024 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1423662639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_627102,Human_RBP_ID_24071764 Human_miRNA_ID_456449,Human_miRNA_ID_458413 77357 RMVar_ID_77357 Human_SNP_ID_195922107 m1A Human chr4 + 99072392 99072391 99072392 CTGTTAAGCTGCTCCTATCACATCACGACAGGATGGACATTATTTTTCTCTTTTGAATTAAATCT CTGTTAAGCTGCTCCTATCACATCACGACAGG_TGGACATTATTTTTCTCTTTTGAATTAAATCT GA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99072168..99072418 32194978 MeRIP-seq:(Medium) rs758796356 Functional Loss DEL dbSNP153 33..33 33 - - - 77358 RMVar_ID_77358 Human_SNP_ID_195923105 m1A Human chr4 + 99076472 99076464 99076472 TTATTGATGTCCACACCAATGATCCGGGAAGCACCAGCCACTTTACAGCCCATGATAACTGCCAA TTATTGATGTCCACACCAATGATCC________CCAGCCACTTTACAGCCCATGATAACTGCCAA CGGGAAGCA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99076351..99076831 32194978 MeRIP-seq:(Medium) rs866099018 Functional Loss DEL dbSNP153 26..33 33 - - - 77359 RMVar_ID_77359 Human_SNP_ID_195923116 m1A Human chr4 + 99076472 99076472 99076472 TTATTGATGTCCACACCAATGATCCGGGAAGCACCAGCCACTTTACAGCCCATGATAACTGCCAA TTATTGATGTCCACACCAATGATCCGGGAAGCCCCAGCCACTTTACAGCCCATGATAACTGCCAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99076351..99076831 32194978 MeRIP-seq:(Medium) rs199508117 Functional Loss SNV dbSNP153 33..33 33 - - - 77360 RMVar_ID_77360 Human_SNP_ID_195924297 m1A Human chr4 - 99081454 99081454 99081454 TACCTATTCAGGATGTCTTTGCATTTGTTTCCAGGTGACACTGTCATCCCACTTTACATCCCACA TACCTATTCAGGATGTCTTTGCATTTGTTTCCGGGTGACACTGTCATCCCACTTTACATCCCACA T C ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99081386..99081707 32194978 MeRIP-seq:(Medium) rs368791998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941407,Human_RBP_ID_22679323 Human_Splice_Rec_585139,Human_Splice_Rec_585153,Human_Splice_Rec_585167,Human_Splice_Rec_585179,Human_Splice_Rec_585191,Human_Splice_Rec_585199,Human_Splice_Rec_585209,Human_Splice_Rec_585219,Human_Splice_Rec_585231,Human_Splice_Rec_585241 RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 77361 RMVar_ID_77361 Human_SNP_ID_195924441 m1A Human chr4 - 99082017 99082017 99082017 TTCCAGTGATCTTGGGACATGAAGGTGCTGGAATTGTGGAAAGTGTTGGTGAGGGAGTTACTAAG TTCCAGTGATCTTGGGACATGAAGGTGCTGGAGTTGTGGAAAGTGTTGGTGAGGGAGTTACTAAG T C ADH5 Ensembl:ENSG00000197894 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99081954..99085201 32194978 MeRIP-seq:(Medium) rs774049639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609848,Human_RBP_ID_941408,Human_RBP_ID_1971004,Human_RBP_ID_5121051,Human_RBP_ID_5394402,Human_RBP_ID_9147909,Human_RBP_ID_18032681,Human_RBP_ID_19013871,Human_RBP_ID_22457720 Human_Splice_Rec_585136,Human_Splice_Rec_585137,Human_Splice_Rec_585164,Human_Splice_Rec_585165,Human_Splice_Rec_585188,Human_Splice_Rec_585189,Human_Splice_Rec_585196,Human_Splice_Rec_585197,Human_Splice_Rec_585206,Human_Splice_Rec_585207,Human_Splice_Rec_585216,Human_Splice_Rec_585217,Human_Splice_Rec_585228,Human_Splice_Rec_585229,Human_Splice_Rec_585238,Human_Splice_Rec_585239,Human_Splice_Rec_585246,Human_Splice_Rec_585252 RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 77362 RMVar_ID_77362 Human_SNP_ID_195925274 m1A Human chr4 - 99085218 99085215 99085219 ATAAACAGCTTATTCCCTTTTTTCCCCACTTCAGGTTATCAAGTGCAAGGCTGCAGTTGCTTGGG ATAAACAGCTTATTCCCTTTTTTCCCCACTT____TTATCAAGTGCAAGGCTGCAGTTGCTTGGG ACCTG A ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:99085176..99085225 26863196 MeRIP-seq:(Medium) rs1405504051 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_19121750 RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 77363 RMVar_ID_77363 Human_SNP_ID_195925276 m1A Human chr4 - 99085218 99085217 99085219 ATAAACAGCTTATTCCCTTTTTTCCCCACTTCAGGTTATCAAGTGCAAGGCTGCAGTTGCTTGGG ATAAACAGCTTATTCCCTTTTTTCCCCACTT__GGTTATCAAGTGCAAGGCTGCAGTTGCTTGGG CTG C ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:99085176..99085225 26863196 MeRIP-seq:(Medium) rs1347801112 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_19121750 RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 77364 RMVar_ID_77364 Human_SNP_ID_195926189 m1A Human chr4 - 99088538 99088538 99088538 TTCTGAAACTGGGCCCCCAGCGAGCGGCTCAGAGGGGCAGAAAGAGAAGGAAGCTTTGTCTCGGC TTCTGAAACTGGGCCCCCAGCGAGCGGCTCAGGGGGGCAGAAAGAGAAGGAAGCTTTGTCTCGGC T C ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:99088532..99088711 26863196 MeRIP-seq:(Medium) rs1560757922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 77365 RMVar_ID_77365 Human_SNP_ID_196133856 m1A Human chr4 - 99946546 99946546 99946546 GCAAGCTATGGAGGGGAACAGGGATGAGGCTGAGAAATGTGTCGAGATCGCCCGGGAGGCCCTGA GCAAGCTATGGAGGGGAACAGGGATGAGGCTGTGAAATGTGTCGAGATCGCCCGGGAGGCCCTGA T A DNAJB14 Ensembl:ENSG00000164031 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:99946480..99946592 26863196 MeRIP-seq:(Medium) rs1346052559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837558,Human_RBP_ID_941325,Human_RBP_ID_7250960,Human_RBP_ID_15009194,Human_RBP_ID_24027275,Human_RBP_ID_26348916 Human_miRNA_ID_2953474,Human_miRNA_ID_2957217 RMVar_hsa_circ_90526,RMVar_hsa_circ_227653 77366 RMVar_ID_77366 Human_SNP_ID_196133858 m1A Human chr4 + 99946548 99946548 99946548 AGGGCCTCCCGGGCGATCTCGACACATTTCTCAGCCTCATCCCTGTTCCCCTCCATAGCTTGCTC AGGGCCTCCCGGGCGATCTCGACACATTTCTCGGCCTCATCCCTGTTCCCCTCCATAGCTTGCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:99946476..99946606 26863196 MeRIP-seq:(Medium) rs1042187472 Functional Loss SNV dbSNP153 33..33 33 - - - 77367 RMVar_ID_77367 Human_SNP_ID_196134979 m1A Human chr4 - 99949742 99949742 99949742 TCCTCCTCCGCTCGCGGGCGTGTGCGCGCCGCAGGCTGGCGGTAAGGCTGGAAAGGACTCCGGAA TCCTCCTCCGCTCGCGGGCGTGTGCGCGCCGCTGGCTGGCGGTAAGGCTGGAAAGGACTCCGGAA T A H2AZ1 Ensembl:ENSG00000164032 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr4:99949701..99949750;chr4:99949626..99949849;chr4:99949718..99949798;chr4:99949651..99949750 26863196,26863410,26863196,32194978 MeRIP-seq:(Medium) rs113550334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940952,Human_RBP_ID_4796078,Human_RBP_ID_5150652,Human_RBP_ID_18195028,Human_RBP_ID_19121758,Human_RBP_ID_22458672,Human_RBP_ID_22679329,Human_RBP_ID_25829847,Human_RBP_ID_27159983,Human_RBP_ID_27721981 Human_Splice_Rec_586243,Human_Splice_Rec_586251,Human_Splice_Rec_586259,Human_Splice_Rec_586267,Human_Splice_Rec_586275 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 77368 RMVar_ID_77368 Human_SNP_ID_196135168 m1A Human chr4 + 99950144 99950139 99950144 TTTTTCTCTCGCCGGCAAAAACCCGCGGAGTCATCGAGCGTCTCTGCGAAGTTTACCATTTCGAA TTTTTCTCTCGCCGGCAAAAACCCGCGG_____TCGAGCGTCTCTGCGAAGTTTACCATTTCGAA GAGTCA G H2AZ1-DT Ensembl:ENSG00000245322 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99950142..99950241 32194978 MeRIP-seq:(Medium) rs1431365148 Functional Loss DEL dbSNP153 29..33 33 - - - Human_Splice_Rec_586279 77369 RMVar_ID_77369 Human_SNP_ID_196135173 m1A Human chr4 + 99950144 99950144 99950144 TTTTTCTCTCGCCGGCAAAAACCCGCGGAGTCATCGAGCGTCTCTGCGAAGTTTACCATTTCGAA TTTTTCTCTCGCCGGCAAAAACCCGCGGAGTCTTCGAGCGTCTCTGCGAAGTTTACCATTTCGAA A T H2AZ1-DT Ensembl:ENSG00000245322 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99950142..99950241 32194978 MeRIP-seq:(Medium) rs765588625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_586279 77370 RMVar_ID_77370 Human_SNP_ID_196135212 m1A Human chr4 - 99950218 99950218 99950218 GGAGTAGGTGGTGGGATCTCACCGTGGGTCCGATTAGCCTTTTCTCTGCCTTGCTTGCTTGAGCT GGAGTAGGTGGTGGGATCTCACCGTGGGTCCGTTTAGCCTTTTCTCTGCCTTGCTTGCTTGAGCT T A H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr4:99950071..99950275;chr4:99949901..99950350 26863196 MeRIP-seq:(Medium) rs1297595979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12154,Human_RBP_ID_249138,Human_RBP_ID_610129,Human_RBP_ID_942119,Human_RBP_ID_1034584,Human_RBP_ID_1207053,Human_RBP_ID_1315040,Human_RBP_ID_1387143,Human_RBP_ID_1633764,Human_RBP_ID_1971068,Human_RBP_ID_3724441,Human_RBP_ID_4795069,Human_RBP_ID_5276261,Human_RBP_ID_5425843,Human_RBP_ID_5448044,Human_RBP_ID_5474925,Human_RBP_ID_5507142,Human_RBP_ID_8581262,Human_RBP_ID_8876141,Human_RBP_ID_9334756,Human_RBP_ID_15009281,Human_RBP_ID_18015162,Human_RBP_ID_18816458,Human_RBP_ID_22095603,Human_RBP_ID_22457730,Human_RBP_ID_22825262,Human_RBP_ID_24027302,Human_RBP_ID_27060621,Human_RBP_ID_27323059 Human_Splice_Rec_586239,Human_Splice_Rec_586241,Human_Splice_Rec_586249,Human_Splice_Rec_586273 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 77371 RMVar_ID_77371 Human_SNP_ID_196135230 m1A Human chr4 - 99950245 99950245 99950245 GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTAGGTGGTGGGATCTCACCGTGGGTCCGATTAGC GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTTGGTGGTGGGATCTCACCGTGGGTCCGATTAGC T A H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:99950201..99950275 26863196 MeRIP-seq:(Medium) rs1263536050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12154,Human_RBP_ID_249138,Human_RBP_ID_283004,Human_RBP_ID_610129,Human_RBP_ID_786238,Human_RBP_ID_837765,Human_RBP_ID_1034584,Human_RBP_ID_1387144,Human_RBP_ID_1633766,Human_RBP_ID_1971068,Human_RBP_ID_3724441,Human_RBP_ID_4795069,Human_RBP_ID_5475863,Human_RBP_ID_5507142,Human_RBP_ID_7250988,Human_RBP_ID_8581262,Human_RBP_ID_9147974,Human_RBP_ID_9334756,Human_RBP_ID_15009286,Human_RBP_ID_18816461,Human_RBP_ID_22095603,Human_RBP_ID_22457730,Human_RBP_ID_22510051,Human_RBP_ID_23213841,Human_RBP_ID_24027302,Human_RBP_ID_24499635 Human_Splice_Rec_586239,Human_Splice_Rec_586241,Human_Splice_Rec_586249,Human_Splice_Rec_586273 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 77372 RMVar_ID_77372 Human_SNP_ID_196135231 m1A Human chr4 - 99950245 99950245 99950245 GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTAGGTGGTGGGATCTCACCGTGGGTCCGATTAGC GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTGGGTGGTGGGATCTCACCGTGGGTCCGATTAGC T C H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:99950201..99950275 26863196 MeRIP-seq:(Medium) rs1263536050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12154,Human_RBP_ID_249138,Human_RBP_ID_283004,Human_RBP_ID_610129,Human_RBP_ID_786238,Human_RBP_ID_837765,Human_RBP_ID_1034584,Human_RBP_ID_1387144,Human_RBP_ID_1633766,Human_RBP_ID_1971068,Human_RBP_ID_3724441,Human_RBP_ID_4795069,Human_RBP_ID_5475863,Human_RBP_ID_5507142,Human_RBP_ID_7250988,Human_RBP_ID_8581262,Human_RBP_ID_9147974,Human_RBP_ID_9334756,Human_RBP_ID_15009286,Human_RBP_ID_18816461,Human_RBP_ID_22095603,Human_RBP_ID_22457730,Human_RBP_ID_22510051,Human_RBP_ID_23213841,Human_RBP_ID_24027302,Human_RBP_ID_24499635 Human_Splice_Rec_586239,Human_Splice_Rec_586241,Human_Splice_Rec_586249,Human_Splice_Rec_586273 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 77373 RMVar_ID_77373 Human_SNP_ID_196135241 m1A Human chr4 - 99950273 99950273 99950273 ATAAAGGGAGCAGGGAAGGCGGGAGACAGCGCAGTTTGAATCGCGGTGCGACGAAGGAGTAGGTG ATAAAGGGAGCAGGGAAGGCGGGAGACAGCGCCGTTTGAATCGCGGTGCGACGAAGGAGTAGGTG T G H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:99950226..99950300 32194978 MeRIP-seq:(Medium) rs1451172108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283004,Human_RBP_ID_4796080,Human_RBP_ID_22457730 Human_Splice_Rec_586265 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 77374 RMVar_ID_77374 Human_SNP_ID_196452052 m1A Human chr4 + 101291380 101291380 101291380 TCTGTATTGGCATGCATTCTAATTTATTATGTAATCTGAGGATTGCCTTCCCAACACATGGTATG TCTGTATTGGCATGCATTCTAATTTATTATGTTATCTGAGGATTGCCTTCCCAACACATGGTATG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:101291378..101291491 26863196 MeRIP-seq:(Medium) rs1453375422 Functional Loss SNV dbSNP153 33..33 33 - - - 77375 RMVar_ID_77375 Human_SNP_ID_196465715 m1A Human chr4 - 101346689 101346689 101346689 GTGGCCTGGGTGCACCGTGTGCCGCAGGCGCCAGGGCAGCTTGCCTCGCCTCGCCTTTCCTCCCC GTGGCCTGGGTGCACCGTGTGCCGCAGGCGCCGGGGCAGCTTGCCTCGCCTCGCCTTTCCTCCCC T C PPP3CA Ensembl:ENSG00000138814 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:101346639..101346757 32194978 MeRIP-seq:(Medium) rs767701439 Functional Loss SNV dbSNP153 33..33 33 - - - 77376 RMVar_ID_77376 Human_SNP_ID_196465863 m1A Human chr4 - 101347005 101346982 101347005 GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGGAGGAGGAGTGAAGGCGGCGGCGGCGGAGGAGGG GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGG_______________________CGGAGGAGGG GCCGCCGCCGCCTTCACTCCTCCT G PPP3CA Ensembl:ENSG00000138814 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:101346761..101347600 26863196 MeRIP-seq:(Medium) rs1157620252 Functional Loss DEL dbSNP153 33..55 33 - - - 77377 RMVar_ID_77377 Human_SNP_ID_196465873 m1A Human chr4 - 101347005 101347005 101347005 GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGGAGGAGGAGTGAAGGCGGCGGCGGCGGAGGAGGG GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGGGGGAGGAGTGAAGGCGGCGGCGGCGGAGGAGGG T C PPP3CA Ensembl:ENSG00000138814 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:101346761..101347600 26863196 MeRIP-seq:(Medium) rs950011396 Functional Loss SNV dbSNP153 33..33 33 - - - 77378 RMVar_ID_77378 Human_SNP_ID_196465874 m1A Human chr4 - 101347005 101347005 101347005 GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGGAGGAGGAGTGAAGGCGGCGGCGGCGGAGGAGGG GAGCGAGTCGGCGGGGCTGGCGGCAGCGGCGGCGGAGGAGTGAAGGCGGCGGCGGCGGAGGAGGG T G PPP3CA Ensembl:ENSG00000138814 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:101346761..101347600 26863196 MeRIP-seq:(Medium) rs950011396 Functional Loss SNV dbSNP153 33..33 33 - - - 77379 RMVar_ID_77379 Human_SNP_ID_196465932 m1A Human chr4 + 101347162 101347162 101347162 AAGCGCACACACGAGCACCCACCCCGGCACGGAGACCCAGCACCGCGGAATGGAGCCCCACGCGC AAGCGCACACACGAGCACCCACCCCGGCACGGGGACCCAGCACCGCGGAATGGAGCCCCACGCGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:101346811..101347457 32194978 MeRIP-seq:(Medium) rs1373403902 Functional Loss SNV dbSNP153 33..33 33 - - - 77380 RMVar_ID_77380 Human_SNP_ID_196698071 m1A Human chr4 + 102290994 102290994 102290994 TCTAGAAATGTGCTCCATAAGATATCCCTACCATGACTTCCATTCTCTTTTGAACGTTCAACCTC TCTAGAAATGTGCTCCATAAGATATCCCTACCGTGACTTCCATTCTCTTTTGAACGTTCAACCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:102290969..102291145 26863196 MeRIP-seq:(Medium) rs887310872 Functional Loss SNV dbSNP153 33..33 33 - - - 77381 RMVar_ID_77381 Human_SNP_ID_196710264 m1A Human chr4 + 102345416 102345416 102345416 CTCTGCGTGTCAACGTAAGACTCGGTCTCTGGATCTCTCTCTCTTTCTGTCTCCCGCCCCCACAA CTCTGCGTGTCAACGTAAGACTCGGTCTCTGGCTCTCTCTCTCTTTCTGTCTCCCGCCCCCACAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:102345338..102345481 26863196 MeRIP-seq:(Medium) rs938647296 Functional Loss SNV dbSNP153 33..33 33 - - - 77382 RMVar_ID_77382 Human_SNP_ID_196780711 m1A Human chr4 - 102635952 102635952 102635952 CTTCATTACTTTGCTCAGAATTTCTTTGCTCCACTGTTGCCAGTAGGCTTTGAGAATGAAAACAC CTTCATTACTTTGCTCAGAATTTCTTTGCTCCGCTGTTGCCAGTAGGCTTTGAGAATGAAAACAC T C MANBA Ensembl:ENSG00000109323 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:102634941..102650545 32194978 MeRIP-seq:(Medium) rs983430522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_610339,Human_RBP_ID_22770307 Human_Splice_Rec_587248,Human_Splice_Rec_587249,Human_Splice_Rec_587280,Human_Splice_Rec_587281,Human_Splice_Rec_587314,Human_Splice_Rec_587315,Human_Splice_Rec_587348,Human_Splice_Rec_587349,Human_Splice_Rec_587382,Human_Splice_Rec_587383,Human_Splice_Rec_587418,Human_Splice_Rec_587419,Human_Splice_Rec_587452,Human_Splice_Rec_587453,Human_Splice_Rec_587486,Human_Splice_Rec_587487,Human_Splice_Rec_587514,Human_Splice_Rec_587515,Human_Splice_Rec_587550,Human_Splice_Rec_587551,Human_Splice_Rec_587580,Human_Splice_Rec_587581,Human_Splice_Rec_587588 RMVar_hsa_circ_12831,RMVar_hsa_circ_269412 77383 RMVar_ID_77383 Human_SNP_ID_196809835 m1A Human chr4 + 102760893 102760893 102760893 ACAGCGCGAGCAGCAGGAGCAGGTGGAGGCGCATCTTGAGATCCCGCGCCACCGAGATGTGGAGA ACAGCGCGAGCAGCAGGAGCAGGTGGAGGCGCTTCTTGAGATCCCGCGCCACCGAGATGTGGAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:102760842..102760912 26863196 MeRIP-seq:(Medium) rs1468077893 Functional Loss SNV dbSNP153 33..33 33 - - - 77384 RMVar_ID_77384 Human_SNP_ID_196820642 m1A Human chr4 - 102802627 102802627 102802627 AGCATACTTTTCTTTTTACAGAATGACAGCCCATATCAAGGCGGTGTATTCTTTTTGACAATTCA AGCATACTTTTCTTTTTACAGAATGACAGCCCTTATCAAGGCGGTGTATTCTTTTTGACAATTCA T A UBE2D3 Ensembl:ENSG00000109332 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:102802576..102802650 26863196 MeRIP-seq:(Medium) rs781691048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1034634,Human_RBP_ID_7252226,Human_RBP_ID_17296772,Human_RBP_ID_17406809,Human_RBP_ID_17521936,Human_RBP_ID_18015411,Human_RBP_ID_22679958,Human_RBP_ID_25830484,Human_RBP_ID_26825550,Human_RBP_ID_27722126 Human_Splice_Rec_587620,Human_Splice_Rec_587630,Human_Splice_Rec_587640,Human_Splice_Rec_587650,Human_Splice_Rec_587662,Human_Splice_Rec_587670,Human_Splice_Rec_587680,Human_Splice_Rec_587694,Human_Splice_Rec_587706,Human_Splice_Rec_587716,Human_Splice_Rec_587728,Human_Splice_Rec_587740,Human_Splice_Rec_587750,Human_Splice_Rec_587764,Human_Splice_Rec_587774,Human_Splice_Rec_587786,Human_Splice_Rec_587798,Human_Splice_Rec_587810,Human_Splice_Rec_587824,Human_Splice_Rec_587834,Human_Splice_Rec_587842,Human_Splice_Rec_587848,Human_Splice_Rec_587856,Human_Splice_Rec_587866,Human_Splice_Rec_587876,Human_Splice_Rec_587884,Human_Splice_Rec_587888,Human_Splice_Rec_587896,Human_Splice_Rec_587904,Human_Splice_Rec_587912 Human_miRNA_ID_2138956 RMVar_hsa_circ_227736,RMVar_hsa_circ_93201,RMVar_hsa_circ_227741,RMVar_hsa_circ_313958,RMVar_hsa_circ_227739,RMVar_hsa_circ_87994,RMVar_hsa_circ_332620,RMVar_hsa_circ_371550,RMVar_hsa_circ_12830,RMVar_hsa_circ_280452,RMVar_hsa_circ_227742,RMVar_hsa_circ_74844,RMVar_hsa_circ_227743,RMVar_hsa_circ_375887,RMVar_hsa_circ_227740,RMVar_hsa_circ_355525,RMVar_hsa_circ_337130,RMVar_hsa_circ_351900,RMVar_hsa_circ_316924,RMVar_hsa_circ_227744 77385 RMVar_ID_77385 Human_SNP_ID_196820643 m1A Human chr4 - 102802627 102802627 102802627 AGCATACTTTTCTTTTTACAGAATGACAGCCCATATCAAGGCGGTGTATTCTTTTTGACAATTCA AGCATACTTTTCTTTTTACAGAATGACAGCCCGTATCAAGGCGGTGTATTCTTTTTGACAATTCA T C UBE2D3 Ensembl:ENSG00000109332 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:102802576..102802650 26863196 MeRIP-seq:(Medium) rs781691048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1034634,Human_RBP_ID_7252226,Human_RBP_ID_17296772,Human_RBP_ID_17406809,Human_RBP_ID_17521936,Human_RBP_ID_18015411,Human_RBP_ID_22679958,Human_RBP_ID_25830484,Human_RBP_ID_26825550,Human_RBP_ID_27722126 Human_Splice_Rec_587620,Human_Splice_Rec_587630,Human_Splice_Rec_587640,Human_Splice_Rec_587650,Human_Splice_Rec_587662,Human_Splice_Rec_587670,Human_Splice_Rec_587680,Human_Splice_Rec_587694,Human_Splice_Rec_587706,Human_Splice_Rec_587716,Human_Splice_Rec_587728,Human_Splice_Rec_587740,Human_Splice_Rec_587750,Human_Splice_Rec_587764,Human_Splice_Rec_587774,Human_Splice_Rec_587786,Human_Splice_Rec_587798,Human_Splice_Rec_587810,Human_Splice_Rec_587824,Human_Splice_Rec_587834,Human_Splice_Rec_587842,Human_Splice_Rec_587848,Human_Splice_Rec_587856,Human_Splice_Rec_587866,Human_Splice_Rec_587876,Human_Splice_Rec_587884,Human_Splice_Rec_587888,Human_Splice_Rec_587896,Human_Splice_Rec_587904,Human_Splice_Rec_587912 Human_miRNA_ID_2138956 RMVar_hsa_circ_227736,RMVar_hsa_circ_93201,RMVar_hsa_circ_227741,RMVar_hsa_circ_313958,RMVar_hsa_circ_227739,RMVar_hsa_circ_87994,RMVar_hsa_circ_332620,RMVar_hsa_circ_371550,RMVar_hsa_circ_12830,RMVar_hsa_circ_280452,RMVar_hsa_circ_227742,RMVar_hsa_circ_74844,RMVar_hsa_circ_227743,RMVar_hsa_circ_375887,RMVar_hsa_circ_227740,RMVar_hsa_circ_355525,RMVar_hsa_circ_337130,RMVar_hsa_circ_351900,RMVar_hsa_circ_316924,RMVar_hsa_circ_227744 77386 RMVar_ID_77386 Human_SNP_ID_196827747 m1A Human chr4 + 102826566 102826565 102826566 CACTCTCTCGGTGTATGCTCAAAGGTCCGGCCAAAACTCTTGATTATCCCGGCGGCGGGGCAGGA CACTCTCTCGGTGTATGCTCAAAGGTCCGGCC_AAACTCTTGATTATCCCGGCGGCGGGGCAGGA CA C UBE2D3-AS1,UBE2D3-AS1:2 RNACentral:URS00009B2292,RNACentral:URS00008C092D lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:102826501..102826713;chr4:102826491..102826677;chr4:102826480..102826680;chr4:102826418..102828092 26863196 MeRIP-seq:(Medium) rs1416723120 Functional Loss DEL dbSNP153 33..33 33 - - - 77387 RMVar_ID_77387 Human_SNP_ID_196827764 m1A Human chr4 - 102826602 102826602 102826602 GCCTGTGTCTGGCAGAGCTGGTGTGAGACGAGACAATCCTGCCCCGCCGCCGGGATAATCAAGAG GCCTGTGTCTGGCAGAGCTGGTGTGAGACGAGTCAATCCTGCCCCGCCGCCGGGATAATCAAGAG T A UBE2D3 Ensembl:ENSG00000109332 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr4:102826551..102826775 26863196,32194978 MeRIP-seq:(Medium) rs1435665819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_610456,Human_RBP_ID_837741,Human_RBP_ID_1633914,Human_RBP_ID_4794672,Human_RBP_ID_5507177,Human_RBP_ID_7252549,Human_RBP_ID_8581606,Human_RBP_ID_15014200,Human_RBP_ID_22095608,Human_RBP_ID_24028293,Human_RBP_ID_27323169 Human_Splice_Rec_587614,Human_Splice_Rec_587656,Human_Splice_Rec_587688,Human_Splice_Rec_587722,Human_Splice_Rec_587734,Human_Splice_Rec_587816,Human_Splice_Rec_587828,Human_Splice_Rec_587850,Human_Splice_Rec_587858,Human_Splice_Rec_587868,Human_Splice_Rec_587890,Human_Splice_Rec_587920 Human_miRNA_ID_2146148,Human_miRNA_ID_2146149,Human_miRNA_ID_2239357,Human_miRNA_ID_2239358,Human_miRNA_ID_2704373,Human_miRNA_ID_2704374,Human_miRNA_ID_2987580,Human_miRNA_ID_2987581,Human_miRNA_ID_3016646,Human_miRNA_ID_3016647,Human_miRNA_ID_3021272,Human_miRNA_ID_3021273,Human_miRNA_ID_3065501,Human_miRNA_ID_3065502 RMVar_hsa_circ_6006,RMVar_hsa_circ_332620,RMVar_hsa_circ_351900,RMVar_hsa_circ_227747,RMVar_hsa_circ_337686,RMVar_hsa_circ_125974,RMVar_hsa_circ_227746,RMVar_hsa_circ_287197,RMVar_hsa_circ_2782,RMVar_hsa_circ_227748 77388 RMVar_ID_77388 Human_SNP_ID_196837992 m1A Human chr4 - 102869101 102869101 102869101 ATGCAGGGAGCTGCACCTTCACGATACGGGCCACGCTCTCCAGCACCATCCTGGCCAGCGGCGTC ATGCAGGGAGCTGCACCTTCACGATACGGGCCTCGCTCTCCAGCACCATCCTGGCCAGCGGCGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:102869055..102869200 26863196 MeRIP-seq:(Medium) rs961514778 Functional Loss SNV dbSNP153 33..33 33 - - - 77389 RMVar_ID_77389 Human_SNP_ID_196858227 m1A Human chr4 + 102955879 102955841 102955879 AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAGAGAAAG _________________________________AGAAAGAAAGAAAGAAAGAAAGAGAGAGAAAG GAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:102955873..102955938 26863196 MeRIP-seq:(Medium) rs1163433220 Functional Loss DEL dbSNP153 1..33 33 - - - 77390 RMVar_ID_77390 Human_SNP_ID_196915078 m1A Human chr4 - 103198312 103198312 103198312 CCTGGGACCAGTTCAGCCTGATAGGATGGCGGAGGAAGGAGCCGTGGCCGTCTGCGTGCGAGTGC CCTGGGACCAGTTCAGCCTGATAGGATGGCGGTGGAAGGAGCCGTGGCCGTCTGCGTGCGAGTGC T A CENPE Ensembl:ENSG00000138778 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:103198250..103198355 26863196 MeRIP-seq:(Medium) rs755136355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249431,Human_RBP_ID_9304206,Human_RBP_ID_9396570,Human_RBP_ID_18424617,Human_RBP_ID_18447072,Human_RBP_ID_23034720,Human_RBP_ID_26349492,Human_RBP_ID_27824325 Human_Splice_Rec_588341,Human_Splice_Rec_588433,Human_Splice_Rec_588529,Human_Splice_Rec_588633 77391 RMVar_ID_77391 Human_SNP_ID_196915099 m1A Human chr4 - 103198349 103198349 103198349 CCCTGAAGTGCCGGCCGCGGAGGGTCCTGGCCATTTTCCTGGGACCAGTTCAGCCTGATAGGATG CCCTGAAGTGCCGGCCGCGGAGGGTCCTGGCCGTTTTCCTGGGACCAGTTCAGCCTGATAGGATG T C CENPE Ensembl:ENSG00000138778 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:103198236..103198371 26863196 MeRIP-seq:(Medium) rs769721702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8882172,Human_RBP_ID_9304207,Human_RBP_ID_18424617 Human_Splice_Rec_588341,Human_Splice_Rec_588433,Human_Splice_Rec_588529,Human_Splice_Rec_588633 77392 RMVar_ID_77392 Human_SNP_ID_197250698 m1A Human chr4 + 104491452 104491440 104491452 CCCCCGCCTCCGCCGCCGCCGCCGCCGCCGCCACCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT CCCCCGCCTCCGCCGCCGCCG____________CCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT GCCGCCGCCGCCA G CXXC4-AS1 Ensembl:ENSG00000245384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr4:104491390..104491498;chr4:104491325..104491558;chr4:104491422..104491564;chr4:104491344..104491544;chr4:104491389..104491454 26863196 MeRIP-seq:(Medium) rs1358031793 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_8266835 77393 RMVar_ID_77393 Human_SNP_ID_197250705 m1A Human chr4 + 104491452 104491452 104491452 CCCCCGCCTCCGCCGCCGCCGCCGCCGCCGCCACCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT CCCCCGCCTCCGCCGCCGCCGCCGCCGCCGCCCCCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT A C CXXC4-AS1 Ensembl:ENSG00000245384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr4:104491390..104491498;chr4:104491325..104491558;chr4:104491422..104491564;chr4:104491344..104491544;chr4:104491389..104491454 26863196 MeRIP-seq:(Medium) rs1023816027 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8266835 77394 RMVar_ID_77394 Human_SNP_ID_197250706 m1A Human chr4 + 104491452 104491452 104491452 CCCCCGCCTCCGCCGCCGCCGCCGCCGCCGCCACCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT CCCCCGCCTCCGCCGCCGCCGCCGCCGCCGCCGCCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCT A G CXXC4-AS1 Ensembl:ENSG00000245384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr4:104491390..104491498;chr4:104491325..104491558;chr4:104491422..104491564;chr4:104491344..104491544;chr4:104491389..104491454 26863196 MeRIP-seq:(Medium) rs1023816027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8266835 77395 RMVar_ID_77395 Human_SNP_ID_197251574 m1A Human chr4 + 104494795 104494795 104494795 GGTGGAAGGAGGAGGAGGTGGGGGGAGAGGAAAGAGTCGAGTGTGAGTGTATGTGTGAGAGCGCG GGTGGAAGGAGGAGGAGGTGGGGGGAGAGGAAGGAGTCGAGTGTGAGTGTATGTGTGAGAGCGCG A G CXXC4-AS1 Ensembl:ENSG00000245384 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:104494746..104494980 26863196 MeRIP-seq:(Medium) rs1331954222 Functional Loss SNV dbSNP153 33..33 33 - - - 77396 RMVar_ID_77396 Human_SNP_ID_522359523 m1A Human chr13 - 18218900 18218900 18218900 GGGACTGGAACTTAGGGGTGTGCCTGGTTAACAAGCATGGAATGAGCTTCTCCTGGACCATCTTC GGGACTGGAACTTAGGGGTGTGCCTGGTTAACGAGCATGGAATGAGCTTCTCCTGGACCATCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:18218895..18219041 26863196 MeRIP-seq:(Medium) rs1281766345 Functional Loss SNV dbSNP153 33..33 33 - - - 77397 RMVar_ID_77397 Human_SNP_ID_522380529 m1A Human chr13 + 18297613 18297613 18297613 CTGGTGGCGGCGGCAGCAGCAGCAGCAGCGGCAGCGGCAGCGGTGGTGGCCGGGCAGCGGCGGCG CTGGTGGCGGCGGCAGCAGCAGCAGCAGCGGCGGCGGCAGCGGTGGTGGCCGGGCAGCGGCGGCG A G KMT5AP1 Ensembl:ENSG00000279730 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:18297548..18297634 26863196 MeRIP-seq:(Medium) rs1282190728 Functional Loss SNV dbSNP153 33..33 33 - - - 77398 RMVar_ID_77398 Human_SNP_ID_522758061 m1A Human chr13 + 19633772 19633772 19633772 GCTGCTAGGATGGAGCAGGTTGCGGAGGGAGCAAGGGTGACCGCAGTCCCTGTGTCAGCTGCCGA GCTGCTAGGATGGAGCAGGTTGCGGAGGGAGCGAGGGTGACCGCAGTCCCTGTGTCAGCTGCCGA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:19633673..19633960 26863196 MeRIP-seq:(Medium) rs886613219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4264769,Human_RBP_ID_9323588,Human_RBP_ID_9367320,Human_RBP_ID_18417758,Human_RBP_ID_18637339,Human_RBP_ID_22041956,Human_RBP_ID_26323973,Human_RBP_ID_27807558 RMVar_hsa_circ_161943,RMVar_hsa_circ_111206 77399 RMVar_ID_77399 Human_SNP_ID_522758111 m1A Human chr13 + 19633858 19633858 19633858 AGTCGAAGAAGGAGTTGGAGTAGTGGGCGAAGATAATGACGCAGCCGCGAGAGGAGCGGAGGCCT AGTCGAAGAAGGAGTTGGAGTAGTGGGCGAAGGTAATGACGCAGCCGCGAGAGGAGCGGAGGCCT A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:19633676..19646452 26863196 MeRIP-seq:(Medium) rs1256736910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196458,Human_RBP_ID_9367321,Human_RBP_ID_22042070,Human_RBP_ID_26323974 RMVar_hsa_circ_161943,RMVar_hsa_circ_111206 77400 RMVar_ID_77400 Human_SNP_ID_522758151 m1A Human chr13 + 19633951 19633943 19633951 TGTGTTCGAGGTGGAGAAGATCCTGGACATGAAGACCGAGGGGGTATGTGGAGGGGCCCCGGCGC TGTGTTCGAGGTGGAGAAGATCCTG________GACCGAGGGGGTATGTGGAGGGGCCCCGGCGC GGACATGAA G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:19633829..19642131 32194978 MeRIP-seq:(Medium) rs1566107290 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_195924,Human_RBP_ID_812506,Human_RBP_ID_3944052,Human_RBP_ID_5174232,Human_RBP_ID_9344887,Human_RBP_ID_9367321,Human_RBP_ID_18469350,Human_RBP_ID_18978750,Human_RBP_ID_22042071,Human_RBP_ID_22919885,Human_RBP_ID_26323975,Human_RBP_ID_26777845,Human_RBP_ID_27807559 Human_Splice_Rec_1448905 RMVar_hsa_circ_161943,RMVar_hsa_circ_111206 77401 RMVar_ID_77401 Human_SNP_ID_522761463 m1A Human chr13 + 19646799 19646798 19646800 AAGGGTGAAATAAGAGATTTAAAGACGAAAACAAGAGAAGATCCCAAAGAAAATAGAAAAACAAA AAGGGTGAAATAAGAGATTTAAAGACGAAAAC__GAGAAGATCCCAAAGAAAATAGAAAAACAAA CAA C MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:19646748..19646848 26863196 MeRIP-seq:(Medium) rs762181938 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_71787,RMVar_hsa_circ_161943,RMVar_hsa_circ_111206,RMVar_hsa_circ_330352,RMVar_hsa_circ_30187,RMVar_hsa_circ_64016,RMVar_hsa_circ_359284,RMVar_hsa_circ_360642 77402 RMVar_ID_77402 Human_SNP_ID_522761569 m1A Human chr13 + 19647089 19647089 19647089 CAGGAGGAAAAAGAAGACCCCGAGAAAGGCTGAGGACACTAGAGAGAACAGGAAGCTAGAGAACA CAGGAGGAAAAAGAAGACCCCGAGAAAGGCTGGGGACACTAGAGAGAACAGGAAGCTAGAGAACA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:19646969..19647109;chr13:19646996..19647150 26863196 MeRIP-seq:(Medium) rs1248442612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2376802,Human_RBP_ID_6260747,Human_RBP_ID_22354683,Human_RBP_ID_24543545,Human_RBP_ID_26323981,Human_RBP_ID_27807565 RMVar_hsa_circ_71787,RMVar_hsa_circ_161943,RMVar_hsa_circ_111206,RMVar_hsa_circ_330352,RMVar_hsa_circ_30187,RMVar_hsa_circ_64016,RMVar_hsa_circ_359284,RMVar_hsa_circ_360642 77403 RMVar_ID_77403 Human_SNP_ID_522761633 m1A Human chr13 + 19647287 19647287 19647287 AGAGAGAGGCCTCTGGTCCACGGACTCAGCCGAGGAGGTAAGGGCCACGGGAGGCAGCAGAAAAC AGAGAGAGGCCTCTGGTCCACGGACTCAGCCGTGGAGGTAAGGGCCACGGGAGGCAGCAGAAAAC A T MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:19646996..19648424 32194978 MeRIP-seq:(Medium) rs765695075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879270,Human_RBP_ID_24543546,Human_RBP_ID_26324268 Human_Splice_Rec_1448909,Human_Splice_Rec_1448931 RMVar_hsa_circ_71787,RMVar_hsa_circ_161943,RMVar_hsa_circ_111206,RMVar_hsa_circ_330352,RMVar_hsa_circ_30187,RMVar_hsa_circ_64016,RMVar_hsa_circ_359284,RMVar_hsa_circ_360642 77404 RMVar_ID_77404 Human_SNP_ID_522772615 m1A Human chr13 - 19687588 19687586 19687589 ATGATAGGTATTTTGGTGCTGCTAAAAAGAGGAGAAAGGGCAGATGGAAGGGTTGGGGCCCTGTG ATGATAGGTATTTTGGTGCTGCTAAAAAGAG___AAAGGGCAGATGGAAGGGTTGGGGCCCTGTG TCTC T PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:19687585..19687677 26863196 MeRIP-seq:(Medium) rs781120381 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9028779 RMVar_hsa_circ_16518 77405 RMVar_ID_77405 Human_SNP_ID_522772617 m1A Human chr13 - 19687588 19687588 19687588 ATGATAGGTATTTTGGTGCTGCTAAAAAGAGGAGAAAGGGCAGATGGAAGGGTTGGGGCCCTGTG ATGATAGGTATTTTGGTGCTGCTAAAAAGAGGTGAAAGGGCAGATGGAAGGGTTGGGGCCCTGTG T A PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:19687585..19687677 26863196 MeRIP-seq:(Medium) rs983084339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9028779 RMVar_hsa_circ_16518 77406 RMVar_ID_77406 Human_SNP_ID_522772618 m1A Human chr13 - 19687588 19687588 19687588 ATGATAGGTATTTTGGTGCTGCTAAAAAGAGGAGAAAGGGCAGATGGAAGGGTTGGGGCCCTGTG ATGATAGGTATTTTGGTGCTGCTAAAAAGAGGGGAAAGGGCAGATGGAAGGGTTGGGGCCCTGTG T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:19687585..19687677 26863196 MeRIP-seq:(Medium) rs983084339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9028779 RMVar_hsa_circ_16518 77407 RMVar_ID_77407 Human_SNP_ID_522822187 m1A Human chr13 - 19863424 19863424 19863424 GGCCGAGGTGAGTGGGGAGGCGGAGATGGGTGAGAGCAGCCTCCGGAGGCTCCCACCGACCCGGG GGCCGAGGTGAGTGGGGAGGCGGAGATGGGTGGGAGCAGCCTCCGGAGGCTCCCACCGACCCGGG T C ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:19863405..19863566 26863196 MeRIP-seq:(Medium) rs1044051561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879275 77408 RMVar_ID_77408 Human_SNP_ID_522848633 m1A Human chr13 + 19958804 19958804 19958804 GTGCGTGTCGCCGAAGGGGGGTGGGCCGGGGGAGGGGAGGTTCGTTCCGCGGAGCCCCAGCCAGA GTGCGTGTCGCCGAAGGGGGGTGGGCCGGGGGGGGGGAGGTTCGTTCCGCGGAGCCCCAGCCAGA A G ZMYM2 Ensembl:ENSG00000121741 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:19958755..19958957 26863196 MeRIP-seq:(Medium) rs1456443382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944055,Human_RBP_ID_4276938,Human_RBP_ID_5522263,Human_RBP_ID_8230208,Human_RBP_ID_18417695,Human_RBP_ID_18935960,Human_RBP_ID_18978440 Human_Splice_Rec_1449095,Human_Splice_Rec_1449137,Human_Splice_Rec_1449195 77409 RMVar_ID_77409 Human_SNP_ID_522911287 m1A Human chr13 - 20192925 20192924 20192925 GCCACGGCGGGAGACAGGTGTTGCGGCCCCGCAGCGCCCGCGCGCTCCTCTCCCCGACTCGGAGC GCCACGGCGGGAGACAGGTGTTGCGGCCCCGC_GCGCCCGCGCGCTCCTCTCCCCGACTCGGAGC CT C GJB2 Ensembl:ENSG00000165474 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr13:20192811..20192926;chr13:20192838..20192926;chr13:20192821..20192950 26863196,26863410,26863196 MeRIP-seq:(Medium) rs983501261 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4265106 77410 RMVar_ID_77410 Human_SNP_ID_522989640 m1A Human chr13 + 20497474 20497472 20497475 CTACACACACCACATATACACACTACACACACACCACCACACACACAACTACACACAGCACACAC CTACACACACCACATATACACACTACACACA___CACCACACACACAACTACACACAGCACACAC ACAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20497471..20497784 26863196 MeRIP-seq:(Medium) rs1289401774 Functional Loss DEL dbSNP153 32..34 33 - - - 77411 RMVar_ID_77411 Human_SNP_ID_522989641 m1A Human chr13 + 20497474 20497474 20497474 CTACACACACCACATATACACACTACACACACACCACCACACACACAACTACACACAGCACACAC CTACACACACCACATATACACACTACACACACCCCACCACACACACAACTACACACAGCACACAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20497471..20497784 26863196 MeRIP-seq:(Medium) rs865858225 Functional Loss SNV dbSNP153 33..33 33 - - - 77412 RMVar_ID_77412 Human_SNP_ID_522989642 m1A Human chr13 + 20497474 20497474 20497474 CTACACACACCACATATACACACTACACACACACCACCACACACACAACTACACACAGCACACAC CTACACACACCACATATACACACTACACACACGCCACCACACACACAACTACACACAGCACACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20497471..20497784 26863196 MeRIP-seq:(Medium) rs865858225 Functional Loss SNV dbSNP153 33..33 33 - - - 77413 RMVar_ID_77413 Human_SNP_ID_522997057 m1A Human chr13 + 20525808 20525808 20525808 CGGCCGCGGAGGACGCCATGGTTGGGCCGGGGACGCGGCGCCGCGGGCGCTGGGACCAGGCGCCG CGGCCGCGGAGGACGCCATGGTTGGGCCGGGGTCGCGGCGCCGCGGGCGCTGGGACCAGGCGCCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:20525700..20525827;chr13:20525755..20525843 26863196 MeRIP-seq:(Medium) rs1439581965 Functional Loss SNV dbSNP153 33..33 33 - - - 77414 RMVar_ID_77414 Human_SNP_ID_523007364 m1A Human chr13 - 20567020 20567020 20567020 GGGTGGGGGCGGAGAACGGCGGGTCAGAGAGAAGGCAGCCCGGTCCCCCTCAGTGGAAGGGAGTG GGGTGGGGGCGGAGAACGGCGGGTCAGAGAGAGGGCAGCCCGGTCCCCCTCAGTGGAAGGGAGTG T C AL590096.1 Ensembl:ENSG00000277020 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:20566866..20567044;chr13:20566866..20567028 26863196 MeRIP-seq:(Medium) rs1224559072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1449571 77415 RMVar_ID_77415 Human_SNP_ID_523007373 m1A Human chr13 - 20567038 20567038 20567038 CGGGAGGCCTGGGGAAGTGGGTGGGGGCGGAGAACGGCGGGTCAGAGAGAAGGCAGCCCGGTCCC CGGGAGGCCTGGGGAAGTGGGTGGGGGCGGAGGACGGCGGGTCAGAGAGAAGGCAGCCCGGTCCC T C AL590096.1 Ensembl:ENSG00000277020 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:20566797..20567069 26863196 MeRIP-seq:(Medium) rs550799281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1449571 77416 RMVar_ID_77416 Human_SNP_ID_523007480 m1A Human chr13 + 20567249 20567249 20567249 CTGGGCCCGAATAACTGTCGCCCGCTTCCCTCAGCGTGAGGTAGGAGAAGGGCGCTGGGGCCTAG CTGGGCCCGAATAACTGTCGCCCGCTTCCCTCTGCGTGAGGTAGGAGAAGGGCGCTGGGGCCTAG A T IFT88 Ensembl:ENSG00000032742 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:20567199..20567299 26863196 MeRIP-seq:(Medium) rs980999482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276548,Human_RBP_ID_18417697,Human_RBP_ID_18978760,Human_RBP_ID_22354847 Human_Splice_Rec_1449577,Human_Splice_Rec_1449625,Human_Splice_Rec_1449677 77417 RMVar_ID_77417 Human_SNP_ID_523044753 m1A Human chr13 - 20718469 20718441 20718469 GCAGGTGTGTGGGGGCAGGTGTGAGCGTGGGCAGGTGTGTGTGGGTGTGTGAGCATGGGCGGGTG GCAGGTGTGTGGGGGCAGGTGTGAGCGTGGGC____________________________GGGTG CGCCCATGCTCACACACCCACACACACCT C lnc-EEF1AKMT1-3 RNACentral:URS00008C1000 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20718421..20718500 26863196 MeRIP-seq:(Medium) rs1383783842 Functional Loss DEL dbSNP153 33..60 33 - - - 77418 RMVar_ID_77418 Human_SNP_ID_523044773 m1A Human chr13 + 20718482 20718482 20718482 TCACACACCCACACACACCTGCCCACGCTCACACCTGCCCCCACACACCTGCCCACACTCAGACA TCACACACCCACACACACCTGCCCACGCTCACCCCTGCCCCCACACACCTGCCCACACTCAGACA A C IL17D Ensembl:ENSG00000172458 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:20718310..20718482 26863196 MeRIP-seq:(Medium) rs1365858262 Functional Loss SNV dbSNP153 33..33 33 - - - 77419 RMVar_ID_77419 Human_SNP_ID_523045126 m1A Human chr13 + 20718998 20718998 20718998 ACGCTCAGACACACCTGCCCACTCACACACCCACACATGCCCATGCTCACACATGCCCACACAGA ACGCTCAGACACACCTGCCCACTCACACACCCCCACATGCCCATGCTCACACATGCCCACACAGA A C IL17D Ensembl:ENSG00000172458 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:20718596..20719477 26863196 MeRIP-seq:(Medium) rs1372327179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196693 77420 RMVar_ID_77420 Human_SNP_ID_523045153 m1A Human chr13 + 20719077 20719073 20719077 CACCTGGCCCACACACACCTGCCCATGCTGACACACAACTACCCATGCTCACACCTGCCCATGCT CACCTGGCCCACACACACCTGCCCATGCT____CACAACTACCCATGCTCACACCTGCCCATGCT TGACA T IL17D Ensembl:ENSG00000172458 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:20719051..20719135 26863196 MeRIP-seq:(Medium) rs1194357071 Functional Loss DEL dbSNP153 30..33 33 - - - 77421 RMVar_ID_77421 Human_SNP_ID_523045260 m1A Human chr13 + 20719273 20719270 20719273 GCACCTGCCCAAACATGCCCACACACACCCCCACACCTGCCCACGCTCAGACACCTGCCCACACT GCACCTGCCCAAACATGCCCACACACACCC___CACCTGCCCACGCTCAGACACCTGCCCACACT CCCA C IL17D Ensembl:ENSG00000172458 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:20719142..20719430 26863196 MeRIP-seq:(Medium) rs1035147521 Functional Loss DEL dbSNP153 31..33 33 - - - 77422 RMVar_ID_77422 Human_SNP_ID_523059481 m1A Human chr13 - 20773766 20773766 20773766 GAGTTTAATTAGCAGTGGCTGGCGGATTCCTGAGGGAAGGAGCTGGCGCCGGCCTGAGAGTGGAT GAGTTTAATTAGCAGTGGCTGGCGGATTCCTGGGGGAAGGAGCTGGCGCCGGCCTGAGAGTGGAT T C EEF1AKMT1 Ensembl:ENSG00000150456 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20773752..20773939 26863196 MeRIP-seq:(Medium) rs1044596489 Functional Loss SNV dbSNP153 33..33 33 - - - 77423 RMVar_ID_77423 Human_SNP_ID_523074186 m1A Human chr13 - 20836426 20836426 20836426 GCAGGAAGAAGCAAAAGAAAATAAGAAAGCCAATTAAGACAAGTGGATGGGAGAACAAGGCAAGG GCAGGAAGAAGCAAAAGAAAATAAGAAAGCCAGTTAAGACAAGTGGATGGGAGAACAAGGCAAGG T C XPO4 Ensembl:ENSG00000132953 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:20836379..20836559 26863196 MeRIP-seq:(Medium) rs1275612103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9721952,Human_RBP_ID_12113023 RMVar_hsa_circ_121993,RMVar_hsa_circ_162081,RMVar_hsa_circ_118617,RMVar_hsa_circ_90423,RMVar_hsa_circ_99243,RMVar_hsa_circ_162085,RMVar_hsa_circ_162086,RMVar_hsa_circ_108101,RMVar_hsa_circ_162087,RMVar_hsa_circ_106399,RMVar_hsa_circ_162091,RMVar_hsa_circ_375682,RMVar_hsa_circ_332001,RMVar_hsa_circ_162093,RMVar_hsa_circ_162092,RMVar_hsa_circ_62861,RMVar_hsa_circ_16322,RMVar_hsa_circ_108811,RMVar_hsa_circ_162106,RMVar_hsa_circ_118799,RMVar_hsa_circ_107632,RMVar_hsa_circ_126228,RMVar_hsa_circ_162108,RMVar_hsa_circ_162109,RMVar_hsa_circ_162112,RMVar_hsa_circ_344895,RMVar_hsa_circ_343649,RMVar_hsa_circ_78096,RMVar_hsa_circ_53181,RMVar_hsa_circ_162115,RMVar_hsa_circ_84288,RMVar_hsa_circ_162116,RMVar_hsa_circ_66253,RMVar_hsa_circ_297282,RMVar_hsa_circ_307391,RMVar_hsa_circ_288935,RMVar_hsa_circ_162119,RMVar_hsa_circ_162120,RMVar_hsa_circ_162121,RMVar_hsa_circ_296886,RMVar_hsa_circ_162118,RMVar_hsa_circ_314877,RMVar_hsa_circ_286142,RMVar_hsa_circ_162123,RMVar_hsa_circ_162124,RMVar_hsa_circ_162125,RMVar_hsa_circ_162122 77424 RMVar_ID_77424 Human_SNP_ID_523074208 m1A Human chr13 + 20836542 20836542 20836542 CTTGGACCACCTCTCCTATTTCCTTAACTTCAATGGCCCCACTCTCCCACAACTTTATCTCCACC CTTGGACCACCTCTCCTATTTCCTTAACTTCAGTGGCCCCACTCTCCCACAACTTTATCTCCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:20836350..20836568 26863196 MeRIP-seq:(Medium) rs949040177 Functional Loss SNV dbSNP153 33..33 33 - - - 77425 RMVar_ID_77425 Human_SNP_ID_523112540 m1A Human chr13 - 20980268 20980268 20980268 TAGGGGCCTCACACAAGGAGTGTTTGGCTTACAGTGAATTGTCCGGTGGGTTTTGCCCACCTCCT TAGGGGCCTCACACAAGGAGTGTTTGGCTTACGGTGAATTGTCCGGTGGGTTTTGCCCACCTCCT T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:20980226..20980275 32194978 MeRIP-seq:(Medium) rs1033957784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_330919,RMVar_hsa_circ_162133 77426 RMVar_ID_77426 Human_SNP_ID_523132388 m1A Human chr13 - 21053318 21053318 21053318 GATTGGGGAGGTCAGGAAGGTCCTTCTGTGGGAGGGGTTCTGGGCTGAGGTTTTAGGAGTAGGAG GATTGGGGAGGTCAGGAAGGTCCTTCTGTGGGGGGGGTTCTGGGCTGAGGTTTTAGGAGTAGGAG T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:21053316..21053430 26863196 MeRIP-seq:(Medium) rs1202852976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 77427 RMVar_ID_77427 Human_SNP_ID_523134419 m1A Human chr13 - 21061427 21061427 21061427 CCGTCCCTGCGGGGCCAGCAGCAGCTCCAGCCACCAGTGCCCGGTCTCCCGGCGCGAGAGGCCCG CCGTCCCTGCGGGGCCAGCAGCAGCTCCAGCCGCCAGTGCCCGGTCTCCCGGCGCGAGAGGCCCG T C LATS2 Ensembl:ENSG00000150457 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:21061378..21061512;chr13:21061379..21061501 26863196 MeRIP-seq:(Medium) rs904473309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4265377 Human_Splice_Rec_1449855 RMVar_hsa_circ_123728,RMVar_hsa_circ_162132 77428 RMVar_ID_77428 Human_SNP_ID_523134436 m1A Human chr13 + 21061495 21061495 21061495 AGCCCCGGGCGGCGGCGGTGGCGTGGACGGCGACTGCTCCATCTTCCCGGGGCGCTCACGCCGCG AGCCCCGGGCGGCGGCGGTGGCGTGGACGGCGTCTGCTCCATCTTCCCGGGGCGCTCACGCCGCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:21061366..21061503 26863196 MeRIP-seq:(Medium) rs962090432 Functional Loss SNV dbSNP153 33..33 33 - - - 77429 RMVar_ID_77429 Human_SNP_ID_523154927 m1A Human chr13 + 21140663 21140663 21140663 ACCCAGGAGGAAATTAAGAAGGAGCCAGAGAAACCGATCGACCGCGAGAAGGTGAAGGCCCCCTC ACCCAGGAGGAAATTAAGAAGGAGCCAGAGAACCCGATCGACCGCGAGAAGGTGAAGGCCCCCTC A C SAP18 Ensembl:ENSG00000150459 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:21140613..21140806 32194978 MeRIP-seq:(Medium) rs550761091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230686,Human_RBP_ID_1481911,Human_RBP_ID_1806235,Human_RBP_ID_3425081,Human_RBP_ID_4276550,Human_RBP_ID_6263322,Human_RBP_ID_17650948,Human_RBP_ID_22438115,Human_RBP_ID_26323995 Human_Splice_Rec_1449873,Human_Splice_Rec_1449879,Human_Splice_Rec_1449885,Human_Splice_Rec_1449891,Human_Splice_Rec_1449893 77430 RMVar_ID_77430 Human_SNP_ID_523154928 m1A Human chr13 + 21140663 21140663 21140663 ACCCAGGAGGAAATTAAGAAGGAGCCAGAGAAACCGATCGACCGCGAGAAGGTGAAGGCCCCCTC ACCCAGGAGGAAATTAAGAAGGAGCCAGAGAAGCCGATCGACCGCGAGAAGGTGAAGGCCCCCTC A G SAP18 Ensembl:ENSG00000150459 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:21140613..21140806 32194978 MeRIP-seq:(Medium) rs550761091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230686,Human_RBP_ID_1481911,Human_RBP_ID_1806235,Human_RBP_ID_3425081,Human_RBP_ID_4276550,Human_RBP_ID_6263322,Human_RBP_ID_17650948,Human_RBP_ID_22438115,Human_RBP_ID_26323995 Human_Splice_Rec_1449873,Human_Splice_Rec_1449879,Human_Splice_Rec_1449885,Human_Splice_Rec_1449891,Human_Splice_Rec_1449893 77431 RMVar_ID_77431 Human_SNP_ID_523155012 m1A Human chr13 + 21140826 21140826 21140826 TCGGAGGCCGCAACGCCTCGGGAAGAGAGATGAGCTCCGGGTTCGCAGCTGGTGTTTTTAACTTC TCGGAGGCCGCAACGCCTCGGGAAGAGAGATGCGCTCCGGGTTCGCAGCTGGTGTTTTTAACTTC A C SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:21140824..21141000;chr13:21140825..21140975 26863196 MeRIP-seq:(Medium) rs1203221384 Functional Loss SNV dbSNP153 33..33 33 - - - 77432 RMVar_ID_77432 Human_SNP_ID_523155045 m1A Human chr13 - 21140878 21140878 21140878 AGACCCGTAGCAACAGTGGGCATGTCTGAGGGAGAGAGAAAACGGAAGGGCAGAAGTTAAAAACA AGACCCGTAGCAACAGTGGGCATGTCTGAGGGGGAGAGAAAACGGAAGGGCAGAAGTTAAAAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:21140876..21141000 26863196 MeRIP-seq:(Medium) rs1195905475 Functional Loss SNV dbSNP153 33..33 33 - - - 77433 RMVar_ID_77433 Human_SNP_ID_523156631 m1A Human chr13 - 21146811 21146811 21146811 TTTACTAAGCTTGTCAGTTCTTTCAAGGTTGCATCCATCCTGGATTTTTTTTAAAAAAGACATTT TTTACTAAGCTTGTCAGTTCTTTCAAGGTTGCGTCCATCCTGGATTTTTTTTAAAAAAGACATTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:21146801..21147436 32194978 MeRIP-seq:(Medium) rs956068163 Functional Loss SNV dbSNP153 33..33 33 - - - 77434 RMVar_ID_77434 Human_SNP_ID_523164905 m1A Human chr13 - 21176904 21176904 21176904 AGGAGCGCAGTCAGGAACATGGTGCCTGCGGAAGAGAGGGACGGGCTTTGCGGAGGCGAACTGGC AGGAGCGCAGTCAGGAACATGGTGCCTGCGGACGAGAGGGACGGGCTTTGCGGAGGCGAACTGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:21176901..21176950 26863196 MeRIP-seq:(Medium) rs1328517448 Functional Loss SNV dbSNP153 33..33 33 - - - 77435 RMVar_ID_77435 Human_SNP_ID_523164962 m1A Human chr13 + 21176978 21176978 21176978 CCGCATTCCCGGCCGTCAGTGGATCGGGAAGCACCGGCGGCCGCGGTTCGTGTCGTTGCGCGCCA CCGCATTCCCGGCCGTCAGTGGATCGGGAAGCGCCGGCGGCCGCGGTTCGTGTCGTTGCGCGCCA A G MRPL57 Ensembl:ENSG00000173141 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:21176694..21177075 26863410 MeRIP-seq:(Medium) rs561593357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276411,Human_RBP_ID_17651061,Human_RBP_ID_19062059,Human_RBP_ID_22438170,Human_RBP_ID_22919917,Human_RBP_ID_23208411 Human_Splice_Rec_1449972 77436 RMVar_ID_77436 Human_SNP_ID_523165010 m1A Human chr13 + 21177076 21177076 21177076 CGGAGAACCATTACTGGCTGAGCATGCCCTACATGACCCGGGAGCAGGAGCGCGGCCACGCCGCG CGGAGAACCATTACTGGCTGAGCATGCCCTACGTGACCCGGGAGCAGGAGCGCGGCCACGCCGCG A G MRPL57 Ensembl:ENSG00000173141 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:21176953..21177198 26863196 MeRIP-seq:(Medium) rs765517221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_433131,Human_RBP_ID_756269,Human_RBP_ID_4276553,Human_RBP_ID_17651019,Human_RBP_ID_22438171,Human_RBP_ID_22919918,Human_RBP_ID_26807365 77437 RMVar_ID_77437 Human_SNP_ID_523195867 m1A Human chr13 - 21298287 21298287 21298287 CCTGCGCCGCAGAGCCGCTGCTCTGGCTCCGAAGCCGCCCGGCTTTTTGGCGCACAGCGTGGTAT CCTGCGCCGCAGAGCCGCTGCTCTGGCTCCGATGCCGCCCGGCTTTTTGGCGCACAGCGTGGTAT T A RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:21298239..21298388 26863196 MeRIP-seq:(Medium) rs1018188794 Functional Loss SNV dbSNP153 33..33 33 - - - 77438 RMVar_ID_77438 Human_SNP_ID_523214208 m1A Human chr13 - 21377245 21377245 21377245 GAGTCAGATCGCAGGCACTAGGGGTGGAGGTCATGTCGGGCAGTCAGATCGCAGGCACTAGGGGT GAGTCAGATCGCAGGCACTAGGGGTGGAGGTCGTGTCGGGCAGTCAGATCGCAGGCACTAGGGGT T C ZDHHC20-IT1,ZDHHC20 Ensembl:ENSG00000236953,Ensembl:ENSG00000180776 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:21377141..21377306;chr13:21377182..21377297 26863196 MeRIP-seq:(Medium) rs1185580263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811999,Human_RBP_ID_8180760 RMVar_hsa_circ_82999,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162152 77439 RMVar_ID_77439 Human_SNP_ID_523214272 m1A Human chr13 + 21377568 21377444 21377568 ACATGACCTCCACCCCTAGTGCCTGCGATCTGACTGCCCGACGTGACCTCCACCCCTAGTGCCTG _________________________________CTGCCCGACGTGACCTCCACCCCTAGTGCCTG TCTGCCCGACGTGACCTCCACCCCTAGTGCCTGCGATCTGACTCTGCCCGACGTGACCTCCACCCCTAGTGCCTGCGATCTGACTCTGCCCGACATGACCTCCACCCCTAGTGCCTGCGATCTGA T lnc-MRPL57-10,lnc-MRPL57-5 RNACentral:URS00008C2CA1,RNACentral:URS00008C24A9 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:21377505..21377613;chr13:21377526..21377616 26863196 MeRIP-seq:(Medium) rs1555253148 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_23588440 77440 RMVar_ID_77440 Human_SNP_ID_523262032 m1A Human chr13 - 21566933 21566933 21566933 TGCAATTTATTTTTCTTTTAGAAAAATGTTGAACATGGAATAATATATATTGGGAAACCGTCTCT TGCAATTTATTTTTCTTTTAGAAAAATGTTGAGCATGGAATAATATATATTGGGAAACCGTCTCT T C MICU2 Ensembl:ENSG00000165487 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:21566883..21582913 26863196 MeRIP-seq:(Medium) rs139051523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1806317 Human_Splice_Rec_1450284,Human_Splice_Rec_1450322,Human_Splice_Rec_1450338,Human_Splice_Rec_1450352 Human_miRNA_ID_150637 RMVar_hsa_circ_8005,RMVar_hsa_circ_38661,RMVar_hsa_circ_344035 77441 RMVar_ID_77441 Human_SNP_ID_523271297 m1A Human chr13 + 21604046 21604046 21604046 TGCCAGGGCCGCGCCGGCCACTGCCGCTGCCAAGGGGCCGGGACTCCGCACAGCCTGTCGGCTGA TGCCAGGGCCGCGCCGGCCACTGCCGCTGCCACGGGGCCGGGACTCCGCACAGCCTGTCGGCTGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:21603995..21604124 26863196 MeRIP-seq:(Medium) rs946163962 Functional Loss SNV dbSNP153 33..33 33 - - - 77442 RMVar_ID_77442 Human_SNP_ID_523271298 m1A Human chr13 + 21604046 21604046 21604046 TGCCAGGGCCGCGCCGGCCACTGCCGCTGCCAAGGGGCCGGGACTCCGCACAGCCTGTCGGCTGA TGCCAGGGCCGCGCCGGCCACTGCCGCTGCCAGGGGGCCGGGACTCCGCACAGCCTGTCGGCTGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:21603995..21604124 26863196 MeRIP-seq:(Medium) rs946163962 Functional Loss SNV dbSNP153 33..33 33 - - - 77443 RMVar_ID_77443 Human_SNP_ID_523271343 m1A Human chr13 + 21604109 21604109 21604109 GACAGCGAGCCCCCGTCGCAGTTTTCCGCCCCAGGCCGCCACCCGCGCGCAGCTACCCGCAGCCG GACAGCGAGCCCCCGTCGCAGTTTTCCGCCCCCGGCCGCCACCCGCGCGCAGCTACCCGCAGCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:21603976..21604175;chr13:21603995..21604164 26863196 MeRIP-seq:(Medium) rs1424086679 Functional Loss SNV dbSNP153 33..33 33 - - - 77444 RMVar_ID_77444 Human_SNP_ID_523277562 m1A Human chr13 - 21628905 21628905 21628905 CTTCTGGAGCTGGAGATGAACTCGGACCTCAAAGCTCAGCTCAGGGAGCTGAATATTACGGCAGC CTTCTGGAGCTGGAGATGAACTCGGACCTCAAGGCTCAGCTCAGGGAGCTGAATATTACGGCAGC T C RPS7P10 Ensembl:ENSG00000226525 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1411977643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4277028 Human_miRNA_ID_1820242,Human_miRNA_ID_1820371,Human_miRNA_ID_1873266,Human_miRNA_ID_1903311 77445 RMVar_ID_77445 Human_SNP_ID_523551891 m1A Human chr13 + 22696629 22696601 22696629 CGGTGGCGGCGGCGGTGGCTGCGCGGCGCTGGAGCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG CGGTG____________________________GCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG GGCGGCGGCGGTGGCTGCGCGGCGCTGGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:22696522..22696712;chr13:22696528..22696748;chr13:22696522..22696745;chr13:22696531..22696741 26863196 MeRIP-seq:(Medium) rs1198416729 Functional Loss DEL dbSNP153 6..33 33 - - - 77446 RMVar_ID_77446 Human_SNP_ID_523551905 m1A Human chr13 + 22696629 22696629 22696629 CGGTGGCGGCGGCGGTGGCTGCGCGGCGCTGGAGCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG CGGTGGCGGCGGCGGTGGCTGCGCGGCGCTGGCGCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:22696522..22696712;chr13:22696528..22696748;chr13:22696522..22696745;chr13:22696531..22696741 26863196 MeRIP-seq:(Medium) rs1020498486 Functional Loss SNV dbSNP153 33..33 33 - - - 77447 RMVar_ID_77447 Human_SNP_ID_523551906 m1A Human chr13 + 22696629 22696629 22696629 CGGTGGCGGCGGCGGTGGCTGCGCGGCGCTGGAGCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG CGGTGGCGGCGGCGGTGGCTGCGCGGCGCTGGGGCGGCGGCGGGGGCCCTGGGGCAGTCCGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:22696522..22696712;chr13:22696528..22696748;chr13:22696522..22696745;chr13:22696531..22696741 26863196 MeRIP-seq:(Medium) rs1020498486 Functional Loss SNV dbSNP153 33..33 33 - - - 77448 RMVar_ID_77448 Human_SNP_ID_523724464 m1A Human chr13 - 23331279 23331279 23331279 GAAGGTGGTGATATCTATGGATCATACCAGCCAACATACACATATGCAATTATTGTACAAGAAGT GAAGGTGGTGATATCTATGGATCATACCAGCCGACATACACATATGCAATTATTGTACAAGAAGT T C SACS Ensembl:ENSG00000151835 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:23331169..23331281 32194978 MeRIP-seq:(Medium) rs112630127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_433358,Human_RBP_ID_995832,Human_RBP_ID_1806347,Human_RBP_ID_8788758,Human_RBP_ID_17244218,Human_RBP_ID_17475834,Human_RBP_ID_27637121 Human_miRNA_ID_351842,Human_miRNA_ID_1289684,Human_miRNA_ID_1426169,Human_miRNA_ID_2633096,Human_miRNA_ID_2772465 Clinvar_Rec_357 RMVar_hsa_circ_95202,RMVar_hsa_circ_162197 77449 RMVar_ID_77449 Human_SNP_ID_523736551 m1A Human chr13 + 23375213 23375213 23375213 GTTCCTTCACATCGCGCACGGTCCAGGACGCCAGCGCCGCGACGGTCCTGCAGCCCACGCAGCCG GTTCCTTCACATCGCGCACGGTCCAGGACGCCGGCGCCGCGACGGTCCTGCAGCCCACGCAGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:23375170..23375482 26863196 MeRIP-seq:(Medium) rs1390931452 Functional Loss SNV dbSNP153 33..33 33 - - - 77450 RMVar_ID_77450 Human_SNP_ID_523861619 m1A Human chr13 - 23889305 23889305 23889305 ACTGCTCTGGTGCTAGAATGCTGTGCGTCGGAAGGCTGGGCGGCTTGGGAGCCAGAGCAGCAGCT ACTGCTCTGGTGCTAGAATGCTGTGCGTCGGACGGCTGGGCGGCTTGGGAGCCAGAGCAGCAGCT T G MIPEP Ensembl:ENSG00000027001 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:23889255..23889398 26863196 MeRIP-seq:(Medium) rs1040016913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879073,Human_RBP_ID_4266243,Human_RBP_ID_22919922,Human_RBP_ID_23588779 Human_miRNA_ID_2083694,Human_miRNA_ID_3010717 RMVar_hsa_circ_92715,RMVar_hsa_circ_162221 77451 RMVar_ID_77451 Human_SNP_ID_524124236 m1A Human chr13 - 24891197 24891197 24891197 GGTGTCCTGAGAGCAAGTGAAGAAAAGGCTGCAAGGAGGAGAGTGACCACCTGTGTCAGGTGTGG GGTGTCCTGAGAGCAAGTGAAGAAAAGGCTGCGAGGAGGAGAGTGACCACCTGTGTCAGGTGTGG T C CENPJ Ensembl:ENSG00000151849 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:24891148..24891261 26863196 MeRIP-seq:(Medium) rs1318014967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23588976 RMVar_hsa_circ_35860,RMVar_hsa_circ_162281,RMVar_hsa_circ_267931,RMVar_hsa_circ_302880 77452 RMVar_ID_77452 Human_SNP_ID_524124262 m1A Human chr13 - 24891297 24891297 24891297 ATGTGTGATACAGCACTGGGCAGGGAGAGGCCAGCAGGGCTGTGAGTAGGCAGGGAGGAGCAGAT ATGTGTGATACAGCACTGGGCAGGGAGAGGCCGGCAGGGCTGTGAGTAGGCAGGGAGGAGCAGAT T C CENPJ Ensembl:ENSG00000151849 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:24890720..24891500 26863196 MeRIP-seq:(Medium) rs1374202550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35860,RMVar_hsa_circ_162281,RMVar_hsa_circ_267931,RMVar_hsa_circ_302880 77453 RMVar_ID_77453 Human_SNP_ID_524125354 m1A Human chr13 + 24895054 24895054 24895054 CTCAGAGGCAAGGCCTCCACGTCCCGCGGGCAAGGCTCAGGCAGAGGCGGCTGCCAGGTCCCGGT CTCAGAGGCAAGGCCTCCACGTCCCGCGGGCATGGCTCAGGCAGAGGCGGCTGCCAGGTCCCGGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:24895004..24895110 32194978 MeRIP-seq:(Medium) rs1228657064 Functional Loss SNV dbSNP153 33..33 33 - - - 77454 RMVar_ID_77454 Human_SNP_ID_524217759 m1A Human chr13 - 25251751 25251751 25251751 TCATAAAGGTTTTGGAGGAACATGTACCATCAATTTGATCGAACACTGCATCCTAGGCAGTCTGT TCATAAAGGTTTTGGAGGAACATGTACCATCATTTTGATCGAACACTGCATCCTAGGCAGTCTGT T A MTMR6 Ensembl:ENSG00000139505 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4312169 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23589099 Human_Splice_Rec_1451594 GWAS_ID_9294,GWAS_ID_9295,GWAS_ID_9296,GWAS_ID_9297,GWAS_ID_9298,GWAS_ID_9299 RMVar_hsa_circ_17934,RMVar_hsa_circ_284668,RMVar_hsa_circ_55478,RMVar_hsa_circ_162288 77455 RMVar_ID_77455 Human_SNP_ID_524217760 m1A Human chr13 - 25251751 25251751 25251751 TCATAAAGGTTTTGGAGGAACATGTACCATCAATTTGATCGAACACTGCATCCTAGGCAGTCTGT TCATAAAGGTTTTGGAGGAACATGTACCATCAGTTTGATCGAACACTGCATCCTAGGCAGTCTGT T C MTMR6 Ensembl:ENSG00000139505 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4312169 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23589099 Human_Splice_Rec_1451594 GWAS_ID_9294,GWAS_ID_9295,GWAS_ID_9296,GWAS_ID_9297,GWAS_ID_9298,GWAS_ID_9299 RMVar_hsa_circ_17934,RMVar_hsa_circ_284668,RMVar_hsa_circ_55478,RMVar_hsa_circ_162288 77456 RMVar_ID_77456 Human_SNP_ID_524233044 m1A Human chr13 + 25312161 25312158 25312162 CATGAACAGAGGAAAGAGAGCTACAGAAAAAAAGGACTGAAAAGGAATAGGGAGACAGCTGGGGG CATGAACAGAGGAAAGAGAGCTACAGAAAA____GACTGAAAAGGAATAGGGAGACAGCTGGGGG AAAAG A NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:25312113..25312286 26863196 MeRIP-seq:(Medium) rs1314436920 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_12117565 RMVar_hsa_circ_45771,RMVar_hsa_circ_162302,RMVar_hsa_circ_315788,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_280106,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162301,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_74188,RMVar_hsa_circ_330721 77457 RMVar_ID_77457 Human_SNP_ID_524233045 m1A Human chr13 + 25312161 25312161 25312161 CATGAACAGAGGAAAGAGAGCTACAGAAAAAAAGGACTGAAAAGGAATAGGGAGACAGCTGGGGG CATGAACAGAGGAAAGAGAGCTACAGAAAAAAGGGACTGAAAAGGAATAGGGAGACAGCTGGGGG A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:25312113..25312286 26863196 MeRIP-seq:(Medium) rs1376720477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12117565 RMVar_hsa_circ_45771,RMVar_hsa_circ_162302,RMVar_hsa_circ_315788,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_280106,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162301,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_74188,RMVar_hsa_circ_330721 77458 RMVar_ID_77458 Human_SNP_ID_524238031 m1A Human chr13 + 25331527 25331527 25331527 ATGCCAAACGCAGCAGCCGTTGCCATGGCTGCAACACTTACACAGCAGCAACAGCCTGCTACAGG ATGCCAAACGCAGCAGCCGTTGCCATGGCTGCGACACTTACACAGCAGCAACAGCCTGCTACAGG A G NUP58 Ensembl:ENSG00000139496 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:25331478..25331617 32194978 MeRIP-seq:(Medium) rs1281691193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_433554,Human_RBP_ID_1482127,Human_RBP_ID_8789162,Human_RBP_ID_9280464,Human_RBP_ID_9367384,Human_RBP_ID_17244312,Human_RBP_ID_17359266,Human_RBP_ID_17475932,Human_RBP_ID_18267063 Human_Splice_Rec_1451651,Human_Splice_Rec_1451703,Human_Splice_Rec_1451729,Human_Splice_Rec_1451771,Human_Splice_Rec_1451793,Human_Splice_Rec_1451799 RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_80243,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_162309,RMVar_hsa_circ_162308,RMVar_hsa_circ_373228,RMVar_hsa_circ_29493,RMVar_hsa_circ_162314,RMVar_hsa_circ_321697,RMVar_hsa_circ_162311,RMVar_hsa_circ_334462,RMVar_hsa_circ_361388 77459 RMVar_ID_77459 Human_SNP_ID_524465135 m1A Human chr13 - 26254188 26254180 26254188 GCTCTCACACACACGCTCACACTCACTCACTCACTCACTCTCCCATACACTCAAACAGAAGGGCA GCTCTCACACACACGCTCACACTCACTCACTC________TCCCATACACTCAAACAGAAGGGCA AGAGTGAGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:26254138..26254419 26863196 MeRIP-seq:(Medium) rs533020430 Functional Loss DEL dbSNP153 33..40 33 - - - 77460 RMVar_ID_77460 Human_SNP_ID_524465136 m1A Human chr13 - 26254188 26254180 26254188 GCTCTCACACACACGCTCACACTCACTCACTCACTCACTCTCCCATACACTCAAACAGAAGGGCA GCTCTCACACACACGCTCACACTCACTCACTC____ACTCTCCCATACACTCAAACAGAAGGGCA AGAGTGAGT AGAGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:26254138..26254419 26863196 MeRIP-seq:(Medium) rs533020430 Functional Loss DEL dbSNP153 33..36 33 - - - 77461 RMVar_ID_77461 Human_SNP_ID_524569460 m1A Human chr13 + 26682726 26682726 26682726 TGCCTTCGTCAGCCCTCTCCAGATGCCCATGCAGCCCCCGTTCCCTGCATCAGCCAGCTCCACGC TGCCTTCGTCAGCCCTCTCCAGATGCCCATGCGGCCCCCGTTCCCTGCATCAGCCAGCTCCACGC A G WASF3 Ensembl:ENSG00000132970 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:26682682..26682863 26863196 MeRIP-seq:(Medium) rs1395410515 Functional Loss SNV dbSNP153 33..33 33 - - - 77462 RMVar_ID_77462 Human_SNP_ID_524691824 m1A Human chr13 - 27163360 27163359 27163360 TGGAGGGATGGGATACCAGATGTAAATAGATAATGTGTTACTCTTAGGCTCTGTAGGTGGTTTGG TGGAGGGATGGGATACCAGATGTAAATAGATA_TGTGTTACTCTTAGGCTCTGTAGGTGGTTTGG AT A USP12 Ensembl:ENSG00000152484 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:27163323..27163469 26863196 MeRIP-seq:(Medium) rs960955893 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12120420 77463 RMVar_ID_77463 Human_SNP_ID_524693950 m1A Human chr13 + 27171669 27171669 27171669 CATCCGGCCAGCGCCATCTTCCACCCAATCACAGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCC CATCCGGCCAGCGCCATCTTCCACCCAATCACGGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:27171621..27171783 26863196 MeRIP-seq:(Medium) rs974869903 Functional Loss SNV dbSNP153 33..33 33 - - - 77464 RMVar_ID_77464 Human_SNP_ID_524693968 m1A Human chr13 + 27171690 27171690 27171690 CACCCAATCACAGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCCGGGCCGCCCGCTCGCACCGCA CACCCAATCACAGCGGCGGCGGCGGGCGGGGGGGGAGGGGAGCCGGGCCGCCCGCTCGCACCGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:27171595..27171835;chr13:27171640..27171986 26863196 MeRIP-seq:(Medium) rs1020428001 Functional Loss SNV dbSNP153 33..33 33 - - - 77465 RMVar_ID_77465 Human_SNP_ID_524694005 m1A Human chr13 - 27171782 27171782 27171782 GGGAGTGCCTGAGCGCCGGCGGCGACGACGGCAGCGGCGGCCCAGCGGGCTCGGTGGTTGGGTCC GGGAGTGCCTGAGCGCCGGCGGCGACGACGGCCGCGGCGGCCCAGCGGGCTCGGTGGTTGGGTCC T G USP12 Ensembl:ENSG00000152484 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:27171576..27171896 26863196 MeRIP-seq:(Medium) rs950903567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276424,Human_RBP_ID_8230216,Human_RBP_ID_18417703 77466 RMVar_ID_77466 Human_SNP_ID_524714153 m1A Human chr13 + 27251795 27251795 27251795 GGTCTGGGCCGTGGGCTGAGAACCGGACTGCGATGTTGCGGCCCTGCGGGGGGACATTTGCGAGA GGTCTGGGCCGTGGGCTGAGAACCGGACTGCGGTGTTGCGGCCCTGCGGGGGGACATTTGCGAGA A G RPL21 Ensembl:ENSG00000122026 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:27251604..27253713;chr13:27251608..27253713 26863196 MeRIP-seq:(Medium) rs959684509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5235861,Human_RBP_ID_5350789,Human_RBP_ID_6266879,Human_RBP_ID_12120638,Human_RBP_ID_17114755 Human_Splice_Rec_1452389 RMVar_hsa_circ_126904,RMVar_hsa_circ_162382,RMVar_hsa_circ_78490,RMVar_hsa_circ_120842,RMVar_hsa_circ_162383,RMVar_hsa_circ_162384 77467 RMVar_ID_77467 Human_SNP_ID_524714154 m1A Human chr13 + 27251795 27251795 27251795 GGTCTGGGCCGTGGGCTGAGAACCGGACTGCGATGTTGCGGCCCTGCGGGGGGACATTTGCGAGA GGTCTGGGCCGTGGGCTGAGAACCGGACTGCGTTGTTGCGGCCCTGCGGGGGGACATTTGCGAGA A T RPL21 Ensembl:ENSG00000122026 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:27251604..27253713;chr13:27251608..27253713 26863196 MeRIP-seq:(Medium) rs959684509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5235861,Human_RBP_ID_5350789,Human_RBP_ID_6266879,Human_RBP_ID_12120638,Human_RBP_ID_17114755 Human_Splice_Rec_1452389 RMVar_hsa_circ_126904,RMVar_hsa_circ_162382,RMVar_hsa_circ_78490,RMVar_hsa_circ_120842,RMVar_hsa_circ_162383,RMVar_hsa_circ_162384 77468 RMVar_ID_77468 Human_SNP_ID_524759845 m1A Human chr13 + 27424683 27424683 27424683 GGAGCCGTGGGCCGGGCGCGCCGGTTCCCGGCACGTGTCTCGGCACGTGGCAGCGCGCCTGGCCC GGAGCCGTGGGCCGGGCGCGCCGGTTCCCGGCTCGTGTCTCGGCACGTGGCAGCGCGCCTGGCCC A T GTF3A Ensembl:ENSG00000122034 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:27424655..27424741 26863410 MeRIP-seq:(Medium) rs1432968778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434015,Human_RBP_ID_4276425,Human_RBP_ID_5235956,Human_RBP_ID_9323441 77469 RMVar_ID_77469 Human_SNP_ID_524759879 m1A Human chr13 + 27424742 27424742 27424742 TGGCCCTGGGCTTGGAGGCGCCGGCGCCCTGGATCCGCCGGCCGTGGTCGCCGAGTCGGTGTCGT TGGCCCTGGGCTTGGAGGCGCCGGCGCCCTGGCTCCGCCGGCCGTGGTCGCCGAGTCGGTGTCGT A C GTF3A Ensembl:ENSG00000122034 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:27424647..27424747 26863410 MeRIP-seq:(Medium) rs772802755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118528,Human_RBP_ID_230594,Human_RBP_ID_4266960,Human_RBP_ID_5235862,Human_RBP_ID_9323599,Human_RBP_ID_9367387 77470 RMVar_ID_77470 Human_SNP_ID_524759880 m1A Human chr13 + 27424742 27424742 27424742 TGGCCCTGGGCTTGGAGGCGCCGGCGCCCTGGATCCGCCGGCCGTGGTCGCCGAGTCGGTGTCGT TGGCCCTGGGCTTGGAGGCGCCGGCGCCCTGGGTCCGCCGGCCGTGGTCGCCGAGTCGGTGTCGT A G GTF3A Ensembl:ENSG00000122034 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:27424647..27424747 26863410 MeRIP-seq:(Medium) rs772802755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118528,Human_RBP_ID_230594,Human_RBP_ID_4266960,Human_RBP_ID_5235862,Human_RBP_ID_9323599,Human_RBP_ID_9367387 77471 RMVar_ID_77471 Human_SNP_ID_524759955 m1A Human chr13 + 27424849 27424849 27424849 CAGCTCCGACCCCGCCGCGCCCCGCGCTTCCCAGGAGGTTCATCTGCTCCTTCCCTGACTGCAGC CAGCTCCGACCCCGCCGCGCCCCGCGCTTCCCGGGAGGTTCATCTGCTCCTTCCCTGACTGCAGC A G GTF3A Ensembl:ENSG00000122034 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:27424689..27424932 26863196 MeRIP-seq:(Medium) rs1440275316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118528,Human_RBP_ID_230595,Human_RBP_ID_434018,Human_RBP_ID_4276569 Human_Splice_Rec_1452445,Human_Splice_Rec_1452461,Human_Splice_Rec_1452471,Human_Splice_Rec_1452493 77472 RMVar_ID_77472 Human_SNP_ID_524761184 m1A Human chr13 + 27429920 27429920 27429920 TGATCAAAAATTCAACACAAAATCAAACTTGAAGAAACATTTTGAACGCAAACATGAAAATCAAC TGATCAAAAATTCAACACAAAATCAAACTTGATGAAACATTTTGAACGCAAACATGAAAATCAAC A T GTF3A Ensembl:ENSG00000122034 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:27429378..27434212 32194978 MeRIP-seq:(Medium) rs1228853743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434025,Human_RBP_ID_1806795,Human_RBP_ID_2379078,Human_RBP_ID_17245700,Human_RBP_ID_17835404,Human_RBP_ID_18528125,Human_RBP_ID_23590083 Human_Splice_Rec_1452448,Human_Splice_Rec_1452449,Human_Splice_Rec_1452464,Human_Splice_Rec_1452465,Human_Splice_Rec_1452474,Human_Splice_Rec_1452475,Human_Splice_Rec_1452488,Human_Splice_Rec_1452489,Human_Splice_Rec_1452496,Human_Splice_Rec_1452497,Human_Splice_Rec_1452506,Human_Splice_Rec_1452507,Human_Splice_Rec_1452520,Human_Splice_Rec_1452521 Human_miRNA_ID_195860,Human_miRNA_ID_696534,Human_miRNA_ID_701473 RMVar_hsa_circ_62246,RMVar_hsa_circ_276264,RMVar_hsa_circ_90243,RMVar_hsa_circ_162389,RMVar_hsa_circ_162387,RMVar_hsa_circ_61306,RMVar_hsa_circ_162386,RMVar_hsa_circ_369847 77473 RMVar_ID_77473 Human_SNP_ID_524766458 m1A Human chr13 + 27449084 27449074 27449085 AAAAATTTTTTTTTAACTTATTCTCCTATGTTAATCCTATGTTAGTCTTCTTCCAGAACTCTAGT AAAAATTTTTTTTTAACTTATTC___________TCCTATGTTAGTCTTCTTCCAGAACTCTAGT CTCCTATGTTAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:27449082..27449333 26863196 MeRIP-seq:(Medium) rs1365163733 Functional Loss DEL dbSNP153 24..34 33 - - - 77474 RMVar_ID_77474 Human_SNP_ID_524766460 m1A Human chr13 + 27449084 27449084 27449084 AAAAATTTTTTTTTAACTTATTCTCCTATGTTAATCCTATGTTAGTCTTCTTCCAGAACTCTAGT AAAAATTTTTTTTTAACTTATTCTCCTATGTTCATCCTATGTTAGTCTTCTTCCAGAACTCTAGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:27449082..27449333 26863196 MeRIP-seq:(Medium) rs113518556 Functional Loss SNV dbSNP153 33..33 33 - - - 77475 RMVar_ID_77475 Human_SNP_ID_524766509 m1A Human chr13 - 27449261 27449259 27449261 GGTGGTCGATGTTTTAAACTGACGGTGGTGACAGTGGATACGGAGAGGACTGGATGGATTCGAGT GGTGGTCGATGTTTTAAACTGACGGTGGTGAC__TGGATACGGAGAGGACTGGATGGATTCGAGT ACT A MTIF3 Ensembl:ENSG00000122033 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:27449112..27449306 26863196 MeRIP-seq:(Medium) rs969781760 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12122131,Human_RBP_ID_23590147 77476 RMVar_ID_77476 Human_SNP_ID_524809695 m1A Human chr13 + 27620491 27620491 27620491 GGAGCGGAGAGCCTGCCCGGCTCCGCTCCGCCAGGAATCGCCGCCGCCGCCGCCGCCGCCGCGGA GGAGCGGAGAGCCTGCCCGGCTCCGCTCCGCCCGGAATCGCCGCCGCCGCCGCCGCCGCCGCGGA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:27620426..27620511 26863410 MeRIP-seq:(Medium) rs1566138267 Functional Loss SNV dbSNP153 33..33 33 - - - 77477 RMVar_ID_77477 Human_SNP_ID_524809861 m1A Human chr13 - 27620833 27620833 27620833 CCACTCTTGGCGGCGGCCGGGGGTGCGCGCAGACACCTAGCCAGCGGGGCTTCCGCAGGGGAATC CCACTCTTGGCGGCGGCCGGGGGTGCGCGCAGTCACCTAGCCAGCGGGGCTTCCGCAGGGGAATC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:27620765..27620849 26863410 MeRIP-seq:(Medium) rs1283805053 Functional Loss SNV dbSNP153 33..33 33 - - - 77478 RMVar_ID_77478 Human_SNP_ID_524809888 m1A Human chr13 + 27620886 27620886 27620886 CGCCAAGAGTGGCACAGCTGGGGAAGGAGTGAACATCCAGAGGAATCGCGGGGCGGGGTGGGGGG CGCCAAGAGTGGCACAGCTGGGGAAGGAGTGAGCATCCAGAGGAATCGCGGGGCGGGGTGGGGGG A G POLR1D Ensembl:ENSG00000186184 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:27620791..27620891 26863410 MeRIP-seq:(Medium) rs943143120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434146,Human_RBP_ID_1482351,Human_RBP_ID_5462717 77479 RMVar_ID_77479 Human_SNP_ID_524810342 m1A Human chr13 - 27621895 27621892 27621896 ATAGCGCGAGGCGCGGAGGCGAAGCAGGAAGCAAGGACCGACCGACGGAAGGCGCGGAGGACGGA ATAGCGCGAGGCGCGGAGGCGAAGCAGGAAG____GACCGACCGACGGAAGGCGCGGAGGACGGA CCTTG C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:27621588..27622186 26863410 MeRIP-seq:(Medium) rs975772183 Functional Loss DEL dbSNP153 32..35 33 - - - 77480 RMVar_ID_77480 Human_SNP_ID_524810344 m1A Human chr13 - 27621895 27621895 27621895 ATAGCGCGAGGCGCGGAGGCGAAGCAGGAAGCAAGGACCGACCGACGGAAGGCGCGGAGGACGGA ATAGCGCGAGGCGCGGAGGCGAAGCAGGAAGCTAGGACCGACCGACGGAAGGCGCGGAGGACGGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:27621588..27622186 26863410 MeRIP-seq:(Medium) rs1279447421 Functional Loss SNV dbSNP153 33..33 33 - - - 77481 RMVar_ID_77481 Human_SNP_ID_524810363 m1A Human chr13 + 27621926 27621926 27621926 TTGCTTCCTGCTTCGCCTCCGCGCCTCGCGCTATGGGACAGAGCCCCCGATCCGCCAGCACCACC TTGCTTCCTGCTTCGCCTCCGCGCCTCGCGCTGTGGGACAGAGCCCCCGATCCGCCAGCACCACC A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:27621881..27622044 26863196 MeRIP-seq:(Medium) rs1056090408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434149,Human_RBP_ID_756155,Human_RBP_ID_812143,Human_RBP_ID_4276574,Human_RBP_ID_12122443,Human_RBP_ID_18638339 Human_Splice_Rec_1452667,Human_Splice_Rec_1452671,Human_Splice_Rec_1452675,Human_Splice_Rec_1452679,Human_Splice_Rec_1452685,Human_Splice_Rec_1452687,Human_Splice_Rec_1452693,Human_Splice_Rec_1452699,Human_Splice_Rec_1452701 Human_miRNA_ID_3069422 RMVar_hsa_circ_114835,RMVar_hsa_circ_162401 77482 RMVar_ID_77482 Human_SNP_ID_524810385 m1A Human chr13 + 27621950 27621950 27621950 CTCGCGCTATGGGACAGAGCCCCCGATCCGCCAGCACCACCTGAGGATCCAGAAACCGCCCCAGC CTCGCGCTATGGGACAGAGCCCCCGATCCGCCCGCACCACCTGAGGATCCAGAAACCGCCCCAGC A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:27621851..27622168 26863196 MeRIP-seq:(Medium) rs545965891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434150,Human_RBP_ID_1482359,Human_RBP_ID_4276574,Human_RBP_ID_8389816,Human_RBP_ID_18638339 Human_Splice_Rec_1452667,Human_Splice_Rec_1452671,Human_Splice_Rec_1452675,Human_Splice_Rec_1452679,Human_Splice_Rec_1452685,Human_Splice_Rec_1452687,Human_Splice_Rec_1452693,Human_Splice_Rec_1452699,Human_Splice_Rec_1452701 RMVar_hsa_circ_114835,RMVar_hsa_circ_162401 77483 RMVar_ID_77483 Human_SNP_ID_524810386 m1A Human chr13 + 27621950 27621950 27621950 CTCGCGCTATGGGACAGAGCCCCCGATCCGCCAGCACCACCTGAGGATCCAGAAACCGCCCCAGC CTCGCGCTATGGGACAGAGCCCCCGATCCGCCGGCACCACCTGAGGATCCAGAAACCGCCCCAGC A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:27621851..27622168 26863196 MeRIP-seq:(Medium) rs545965891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434150,Human_RBP_ID_1482359,Human_RBP_ID_4276574,Human_RBP_ID_8389816,Human_RBP_ID_18638339 Human_Splice_Rec_1452667,Human_Splice_Rec_1452671,Human_Splice_Rec_1452675,Human_Splice_Rec_1452679,Human_Splice_Rec_1452685,Human_Splice_Rec_1452687,Human_Splice_Rec_1452693,Human_Splice_Rec_1452699,Human_Splice_Rec_1452701 RMVar_hsa_circ_114835,RMVar_hsa_circ_162401 77484 RMVar_ID_77484 Human_SNP_ID_524816610 m1A Human chr13 + 27648427 27648427 27648427 CTGCTTAAGGAGGCAAAACGTGGGAAAACTAGAGCTGAAACAATGGGACCCATGGGTTGGTAAGT CTGCTTAAGGAGGCAAAACGTGGGAAAACTAGGGCTGAAACAATGGGACCCATGGGTTGGTAAGT A G POLR1D Ensembl:ENSG00000186184 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:27648310..27648475 26863196 MeRIP-seq:(Medium) rs745353709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1452654,Human_Splice_Rec_1452658,Human_Splice_Rec_1452659,Human_Splice_Rec_1452662,Human_Splice_Rec_1452663,Human_Splice_Rec_1452666,Human_Splice_Rec_1452668,Human_Splice_Rec_1452669,Human_Splice_Rec_1452672,Human_Splice_Rec_1452673,Human_Splice_Rec_1452676,Human_Splice_Rec_1452677,Human_Splice_Rec_1452680,Human_Splice_Rec_1452681,Human_Splice_Rec_1452688,Human_Splice_Rec_1452689,Human_Splice_Rec_1452696,Human_Splice_Rec_1452697,Human_Splice_Rec_1452705,Human_Splice_Rec_1452707 77485 RMVar_ID_77485 Human_SNP_ID_524891703 m1A Human chr13 + 27945464 27945464 27945464 CTTGAAATGCTGCATTTCCAAGGTGAAGATGTATGGGCACATGTTATGGCAGATTGAAAAGGATC CTTGAAATGCTGCATTTCCAAGGTGAAGATGTCTGGGCACATGTTATGGCAGATTGAAAAGGATC A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs771065359 Functional Loss SNV dbSNP153 33..33 33 - - - 77486 RMVar_ID_77486 Human_SNP_ID_524891704 m1A Human chr13 + 27945464 27945464 27945464 CTTGAAATGCTGCATTTCCAAGGTGAAGATGTATGGGCACATGTTATGGCAGATTGAAAAGGATC CTTGAAATGCTGCATTTCCAAGGTGAAGATGTGTGGGCACATGTTATGGCAGATTGAAAAGGATC A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs771065359 Functional Loss SNV dbSNP153 33..33 33 - - - 77487 RMVar_ID_77487 Human_SNP_ID_524942294 m1A Human chr13 + 28138277 28138277 28138277 AGGAACCAGAGCGCGAGAGAGCGAGTGGAGGCAGAATTTAAAAATAAACCGGCCCCTCCGCCTTC AGGAACCAGAGCGCGAGAGAGCGAGTGGAGGCCGAATTTAAAAATAAACCGGCCCCTCCGCCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:28138229..28138425 26863196 MeRIP-seq:(Medium) rs1008039974 Functional Loss SNV dbSNP153 33..33 33 - - - 77488 RMVar_ID_77488 Human_SNP_ID_524942492 m1A Human chr13 - 28138646 28138646 28138646 GAGGCCGCCGCCACTGTTCATGGCAACGCCGCAGCCTCGTCTTCCGCCGCCGCCCGAGGAGCCGC GAGGCCGCCGCCACTGTTCATGGCAACGCCGCCGCCTCGTCTTCCGCCGCCGCCCGAGGAGCCGC T G PAN3-AS1,PAN3-AS1:2,PAN3-AS1:3,PAN3-AS1:4 RNACentral:URS00008C35BB,RNACentral:URS0000D59C08,RNACentral:URS0000D5A35D,RNACentral:URS000075C6DE lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:28138505..28138754 26863196 MeRIP-seq:(Medium) rs1269575774 Functional Loss SNV dbSNP153 33..33 33 - - - 77489 RMVar_ID_77489 Human_SNP_ID_525070791 m1A Human chr13 - 28659022 28659022 28659022 CGCGGGACGCCGGAGGGAGCTGCGCGGGGCCGAGGCTCCCACGCTTGCAATCCCAAGGGACCCAG CGCGGGACGCCGGAGGGAGCTGCGCGGGGCCGCGGCTCCCACGCTTGCAATCCCAAGGGACCCAG T G lnc-SLC46A3-7,lnc-SLC46A3-7:2 RNACentral:URS0000D589B0,RNACentral:URS0000D59E14 lincRNA,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:28658943..28659057 26863196 MeRIP-seq:(Medium) rs942652654 Functional Loss SNV dbSNP153 33..33 33 - - - 77490 RMVar_ID_77490 Human_SNP_ID_525070909 m1A Human chr13 - 28659189 28659189 28659189 GCGTGGAACTCCAGCCGCCCGGGTACCCACTCACCATCTTCCGCAGCTCTGCGAACAGCCTCTCT GCGTGGAACTCCAGCCGCCCGGGTACCCACTCTCCATCTTCCGCAGCTCTGCGAACAGCCTCTCT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:28659126..28659255 26863410 MeRIP-seq:(Medium) rs113700550 Functional Loss SNV dbSNP153 33..33 33 - - - 77491 RMVar_ID_77491 Human_SNP_ID_525286189 m1A Human chr13 - 29513997 29513997 29513997 GCCAGATGAGTACCACAAAACAGTGTGTCCCCAGCAGCTCCCCACCCCAGAGCCAAATGACAGTA GCCAGATGAGTACCACAAAACAGTGTGTCCCCGGCAGCTCCCCACCCCAGAGCCAAATGACAGTA T C SLC7A1 Ensembl:ENSG00000139514 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:29513948..29514093 26863196 MeRIP-seq:(Medium) rs1164929343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38013,Human_RBP_ID_434558,Human_RBP_ID_6269115,Human_RBP_ID_8180476,Human_RBP_ID_12126780,Human_RBP_ID_17245710,Human_RBP_ID_17477905,Human_RBP_ID_26426549,Human_RBP_ID_27427378 Human_miRNA_ID_842116,Human_miRNA_ID_1356477,Human_miRNA_ID_2367509,Human_miRNA_ID_2434404,Human_miRNA_ID_2685061,Human_miRNA_ID_2726009,Human_miRNA_ID_3015302 RMVar_hsa_circ_88762,RMVar_hsa_circ_109649,RMVar_hsa_circ_126005,RMVar_hsa_circ_115769,RMVar_hsa_circ_105603,RMVar_hsa_circ_107463,RMVar_hsa_circ_102343,RMVar_hsa_circ_162496,RMVar_hsa_circ_162500,RMVar_hsa_circ_79863,RMVar_hsa_circ_80846,RMVar_hsa_circ_162501,RMVar_hsa_circ_162502,RMVar_hsa_circ_162498,RMVar_hsa_circ_162499,RMVar_hsa_circ_162497,RMVar_hsa_circ_162494,RMVar_hsa_circ_162495 77492 RMVar_ID_77492 Human_SNP_ID_525286361 m1A Human chr13 - 29514544 29514544 29514544 CATCTACTTTGGCTATGGCCTGTGGCACAGCGAGGAGGCGTCCCTGGATGCCGACCAAGCAAGGA CATCTACTTTGGCTATGGCCTGTGGCACAGCGGGGAGGCGTCCCTGGATGCCGACCAAGCAAGGA T C SLC7A1 Ensembl:ENSG00000139514 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:29514353..29516158 32194978 MeRIP-seq:(Medium) rs761334432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756085,Human_RBP_ID_880108,Human_RBP_ID_1482554,Human_RBP_ID_6269133,Human_RBP_ID_8789488,Human_RBP_ID_12126795,Human_RBP_ID_22757501 Human_Splice_Rec_1453338 RMVar_hsa_circ_88762,RMVar_hsa_circ_109649,RMVar_hsa_circ_126005,RMVar_hsa_circ_115769,RMVar_hsa_circ_105603,RMVar_hsa_circ_107463,RMVar_hsa_circ_102343,RMVar_hsa_circ_162496,RMVar_hsa_circ_162500,RMVar_hsa_circ_79863,RMVar_hsa_circ_80846,RMVar_hsa_circ_162501,RMVar_hsa_circ_162502,RMVar_hsa_circ_162498,RMVar_hsa_circ_162499,RMVar_hsa_circ_162497,RMVar_hsa_circ_162494,RMVar_hsa_circ_162495 77493 RMVar_ID_77493 Human_SNP_ID_525305943 m1A Human chr13 - 29595281 29595281 29595281 GTGGCGAGGGCCCCCGCGCCGGGAACGCTGCCATCCTCTGGGAAGGGCCAGGACCAGGGCCGGGC GTGGCGAGGGCCCCCGCGCCGGGAACGCTGCCCTCCTCTGGGAAGGGCCAGGACCAGGGCCGGGC T G SLC7A1 Ensembl:ENSG00000139514 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:29595231..29595453 26863196 MeRIP-seq:(Medium) rs1282131393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439472,Human_RBP_ID_5235867,Human_RBP_ID_5350804,Human_RBP_ID_18457489 RMVar_hsa_circ_80846,RMVar_hsa_circ_162494,RMVar_hsa_circ_112876,RMVar_hsa_circ_162504,RMVar_hsa_circ_108714,RMVar_hsa_circ_162510 77494 RMVar_ID_77494 Human_SNP_ID_525306043 m1A Human chr13 - 29595565 29595565 29595565 GGCAGGCGCGCACGCGGCCGCGGGCTCCCGCTAACCGCAGCCTCCACTCCTCTCCCCGCGCGCCG GGCAGGCGCGCACGCGGCCGCGGGCTCCCGCTGACCGCAGCCTCCACTCCTCTCCCCGCGCGCCG T C SLC7A1 Ensembl:ENSG00000139514 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr13:29595514..29595671;chr13:29595401..29595725 26863196,26863410 MeRIP-seq:(Medium) rs1178560373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4267673,Human_RBP_ID_5438425 RMVar_hsa_circ_80846,RMVar_hsa_circ_162494,RMVar_hsa_circ_112876,RMVar_hsa_circ_162504,RMVar_hsa_circ_108714,RMVar_hsa_circ_162510 77495 RMVar_ID_77495 Human_SNP_ID_525306045 m1A Human chr13 + 29595572 29595572 29595572 CGGGGAGAGGAGTGGAGGCTGCGGTTAGCGGGAGCCCGCGGCCGCGTGCGCGCCTGCCAGGTAGT CGGGGAGAGGAGTGGAGGCTGCGGTTAGCGGGTGCCCGCGGCCGCGTGCGCGCCTGCCAGGTAGT A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr13:29595485..29595614;chr13:29595401..29595701 26863196,26863410 MeRIP-seq:(Medium) rs1243489499 Functional Loss SNV dbSNP153 33..33 33 - - - 77496 RMVar_ID_77496 Human_SNP_ID_525367942 m1A Human chr13 - 29850465 29850463 29850466 TCTGAGAGGAAACCATTCCCGGGCTGAGGAGAAGGAGGACCCGGCCTCTTCCGGGGACCAGCCGA TCTGAGAGGAAACCATTCCCGGGCTGAGGAG___GAGGACCCGGCCTCTTCCGGGGACCAGCCGA CCTT C UBL3 Ensembl:ENSG00000122042 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:29850185..29850634 26863196 MeRIP-seq:(Medium) rs918563656 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_434663,Human_RBP_ID_812425,Human_RBP_ID_880331,Human_RBP_ID_4276437 RMVar_hsa_circ_98192,RMVar_hsa_circ_162513,RMVar_hsa_circ_102651,RMVar_hsa_circ_162515 77497 RMVar_ID_77497 Human_SNP_ID_525367949 m1A Human chr13 - 29850493 29850493 29850493 AGTGAAGGAGGAGGAGGAGAAACAAAGCTCTGAGAGGAAACCATTCCCGGGCTGAGGAGAAGGAG AGTGAAGGAGGAGGAGGAGAAACAAAGCTCTGGGAGGAAACCATTCCCGGGCTGAGGAGAAGGAG T C UBL3 Ensembl:ENSG00000122042 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:29850087..29850634 26863196 MeRIP-seq:(Medium) rs1430966813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4278481 RMVar_hsa_circ_98192,RMVar_hsa_circ_162513,RMVar_hsa_circ_102651,RMVar_hsa_circ_162515 77498 RMVar_ID_77498 Human_SNP_ID_525367954 m1A Human chr13 - 29850508 29850506 29850509 CGTGTGGGACTGAAAAGTGAAGGAGGAGGAGGAGAAACAAAGCTCTGAGAGGAAACCATTCCCGG CGTGTGGGACTGAAAAGTGAAGGAGGAGGAG___AAACAAAGCTCTGAGAGGAAACCATTCCCGG TCTC T UBL3 Ensembl:ENSG00000122042 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:29850075..29850636 26863196 MeRIP-seq:(Medium) rs1054560899 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_98192,RMVar_hsa_circ_162513,RMVar_hsa_circ_102651,RMVar_hsa_circ_162515 77499 RMVar_ID_77499 Human_SNP_ID_147110070 m1A Human chr3 - 105367184 105367171 105367184 CCCCCAACTCCTCCTCCCTCCCGGTCAACACCAGCCCACGGGCCCTTCGGCTGCTCCTCCGGGGA CCCCCAACTCCTCCTCCCTCCCGGTCAACACC_____________TTCGGCTGCTCCTCCGGGGA AGGGCCCGTGGGCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:105367134..105367275 26863196 MeRIP-seq:(Medium) rs1251124393 Functional Loss DEL dbSNP153 33..45 33 - - - 77500 RMVar_ID_77500 Human_SNP_ID_147230489 m1A Human chr3 - 105867572 105867572 105867572 CTGCCTTTTAAAGAACTAAAATTCCAGATGGCAAACTCAATGAATGGCAGAAACCCTGGTGGTCG CTGCCTTTTAAAGAACTAAAATTCCAGATGGCGAACTCAATGAATGGCAGAAACCCTGGTGGTCG T C CBLB Ensembl:ENSG00000114423 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:105867524..105867612 26863196 MeRIP-seq:(Medium) rs1224150530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_461052,Human_Splice_Rec_461188,Human_Splice_Rec_461226,Human_Splice_Rec_461320,Human_Splice_Rec_461332,Human_Splice_Rec_461338,Human_Splice_Rec_461344,Human_Splice_Rec_461350 RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_62834,RMVar_hsa_circ_80376,RMVar_hsa_circ_220165 77501 RMVar_ID_77501 Human_SNP_ID_147633668 m1A Human chr3 + 107523277 107523277 107523277 GGCAGCCGGTAGGGTGGACTTGAGGAAGACGGAGGGAACCCCGCGCGTCCGGAGCCGCCGCCAGC GGCAGCCGGTAGGGTGGACTTGAGGAAGACGGGGGGAACCCCGCGCGTCCGGAGCCGCCGCCAGC A G BBX Ensembl:ENSG00000114439 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:107523271..107523358 26863196 MeRIP-seq:(Medium) rs1403315257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78880,RMVar_hsa_circ_85695,RMVar_hsa_circ_220173,RMVar_hsa_circ_220174 77502 RMVar_ID_77502 Human_SNP_ID_147633922 m1A Human chr3 - 107524084 107524084 107524084 TAAACTTATTGACACAACATAATCCCACATTCAAGCAAAATCCTGACACAGCCTCCCTCCTCCTC TAAACTTATTGACACAACATAATCCCACATTCTAGCAAAATCCTGACACAGCCTCCCTCCTCCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:107524083..107524167 26863196 MeRIP-seq:(Medium) rs1375186780 Functional Loss SNV dbSNP153 33..33 33 - - - 77503 RMVar_ID_77503 Human_SNP_ID_147644662 m1A Human chr3 - 107569503 107569503 107569503 CCCAGTAATTTTCCACTACCTACCCAAATCCTATAAAACGGCCCCACCCCTATCTCCCTTTACTG CCCAGTAATTTTCCACTACCTACCCAAATCCTGTAAAACGGCCCCACCCCTATCTCCCTTTACTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:107569492..107569578 26863196 MeRIP-seq:(Medium) rs1275474115 Functional Loss SNV dbSNP153 33..33 33 - - - 77504 RMVar_ID_77504 Human_SNP_ID_147644949 m1A Human chr3 + 107570770 107570770 107570770 AGGAGGGGAGAGGTCAGATGGGTCTGCAGAAAAGGAGGATTCAAAGGACTCAAGAGTTTGGGGTG AGGAGGGGAGAGGTCAGATGGGTCTGCAGAAAGGGAGGATTCAAAGGACTCAAGAGTTTGGGGTG A G BBX Ensembl:ENSG00000114439 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:107570599..107570923 26863196 MeRIP-seq:(Medium) rs1318418296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2731741 RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 77505 RMVar_ID_77505 Human_SNP_ID_147645025 m1A Human chr3 + 107571082 107571080 107571082 AGACGCTTAGGTTTTAGGTCAGGCAAGAGTTAAAGAGGTTTTAAGTTTTTGAGAACACAGGCTAA AGACGCTTAGGTTTTAGGTCAGGCAAGAGTT__AGAGGTTTTAAGTTTTTGAGAACACAGGCTAA TAA T BBX Ensembl:ENSG00000114439 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:107571049..107571320 26863196 MeRIP-seq:(Medium) rs1000878034 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 77506 RMVar_ID_77506 Human_SNP_ID_147649347 m1A Human chr3 + 107588239 107588239 107588239 CTAAGGCTTTATGGAGGGGAGGTGTATGAGCCAGGTCTTAGATGATGGTTAGGCCTTGAGGAGGT CTAAGGCTTTATGGAGGGGAGGTGTATGAGCCCGGTCTTAGATGATGGTTAGGCCTTGAGGAGGT A C BBX Ensembl:ENSG00000114439 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:107588235..107588452 26863196 MeRIP-seq:(Medium) rs748372534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2731851,Human_RBP_ID_7101242 RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 77507 RMVar_ID_77507 Human_SNP_ID_147649348 m1A Human chr3 + 107588239 107588239 107588239 CTAAGGCTTTATGGAGGGGAGGTGTATGAGCCAGGTCTTAGATGATGGTTAGGCCTTGAGGAGGT CTAAGGCTTTATGGAGGGGAGGTGTATGAGCCTGGTCTTAGATGATGGTTAGGCCTTGAGGAGGT A T BBX Ensembl:ENSG00000114439 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:107588235..107588452 26863196 MeRIP-seq:(Medium) rs748372534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2731851,Human_RBP_ID_7101242 RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 77508 RMVar_ID_77508 Human_SNP_ID_147698925 m1A Human chr3 - 107801252 107801252 107801252 AACCTGTGCACATTTTCCATGGCTGCCACTTCAGCCAGCGCAGCGAGGCTAAAGAACGCAGACAC AACCTGTGCACATTTTCCATGGCTGCCACTTCCGCCAGCGCAGCGAGGCTAAAGAACGCAGACAC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:107801201..107801300 32194978 MeRIP-seq:(Medium) rs756694175 Functional Loss SNV dbSNP153 33..33 33 - - - 77509 RMVar_ID_77509 Human_SNP_ID_147767649 m1A Human chr3 - 108090974 108090974 108090974 GTGACGCGCGGCGGCGGTCGGTCCTGCCTGTAACGGCGGCGGCGGCTGCTGCTCCGGACACCTGC GTGACGCGCGGCGGCGGTCGGTCCTGCCTGTAGCGGCGGCGGCGGCTGCTGCTCCGGACACCTGC T C CD47 Ensembl:ENSG00000196776 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:108090834..108091025;chr3:108090851..108091025 26863196 MeRIP-seq:(Medium) rs895357427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248664,Human_RBP_ID_585117,Human_RBP_ID_4716483,Human_RBP_ID_9333799 77510 RMVar_ID_77510 Human_SNP_ID_147767651 m1A Human chr3 + 108090978 108090978 108090978 GTGTCCGGAGCAGCAGCCGCCGCCGCCGTTACAGGCAGGACCGACCGCCGCCGCGCGTCACAGGC GTGTCCGGAGCAGCAGCCGCCGCCGCCGTTACGGGCAGGACCGACCGCCGCCGCGCGTCACAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:108090851..108091025;chr3:108090851..108091050;chr3:108080306..108091050 26863196 MeRIP-seq:(Medium) rs1281620633 Functional Loss SNV dbSNP153 33..33 33 - - - 77511 RMVar_ID_77511 Human_SNP_ID_147797738 m1A Human chr3 - 108219531 108219531 108219531 TGCACTGCCTACCAACCCTGGCGAACAGTTCTACATGTTTTGTACTCTTGCTGCTTGGTTGATTA TGCACTGCCTACCAACCCTGGCGAACAGTTCTGCATGTTTTGTACTCTTGCTGCTTGGTTGATTA T C IFT57 Ensembl:ENSG00000114446 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:108219480..108222372 32194978 MeRIP-seq:(Medium) rs926516428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_585159,Human_RBP_ID_23958051,Human_RBP_ID_27042488 Human_Splice_Rec_465194,Human_Splice_Rec_465228,Human_Splice_Rec_465236 Human_miRNA_ID_1241602,Human_miRNA_ID_1457389 RMVar_hsa_circ_19571,RMVar_hsa_circ_21949 77512 RMVar_ID_77512 Human_SNP_ID_147798460 m1A Human chr3 - 108222346 108222346 108222346 CTTAGGCCGCAGAGGTCTGTGGGCCTGAGCCCACGCTGGACTCTGTCCGTTCTGCGATGACTGCT CTTAGGCCGCAGAGGTCTGTGGGCCTGAGCCCGCGCTGGACTCTGTCCGTTCTGCGATGACTGCT T C IFT57 Ensembl:ENSG00000114446 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:108222299..108222397 26863196 MeRIP-seq:(Medium) rs775267915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248191,Human_RBP_ID_585164,Human_RBP_ID_1615375,Human_RBP_ID_4757375,Human_RBP_ID_9129223 77513 RMVar_ID_77513 Human_SNP_ID_147873441 m1A Human chr3 - 108545821 108545818 108545822 CATGCATCCTTTTTGAAAAGTTACTGAAATATATAATAGGTATTGGGAAGAGATTTTTGGTGTGT CATGCATCCTTTTTGAAAAGTTACTGAAATA____ATAGGTATTGGGAAGAGATTTTTGGTGTGT TTATA T - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1452426926 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_23958114 77514 RMVar_ID_77514 Human_SNP_ID_147874663 m1A Human chr3 + 108551309 108551309 108551309 AACGACCTTCTAATTGTGCCTTTTGAACCTCTAGGGAGGAAGCCTAAGGAATTGGGGTTGGGGGA AACGACCTTCTAATTGTGCCTTTTGAACCTCTGGGGAGGAAGCCTAAGGAATTGGGGTTGGGGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:108551261..108554394 32194978 MeRIP-seq:(Medium) rs746921385 Functional Loss SNV dbSNP153 33..33 33 - - - 77515 RMVar_ID_77515 Human_SNP_ID_147877670 m1A Human chr3 - 108563243 108563243 108563243 CTGCTTCTTTTTTGGTTTCTGATTTATTTAGGACCCACGTTTGATTACTCCTTTGGCTTTTGCTT CTGCTTCTTTTTTGGTTTCTGATTTATTTAGGGCCCACGTTTGATTACTCCTTTGGCTTTTGCTT T C CIP2A Ensembl:ENSG00000163507 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:108563195..108566498 32194978 MeRIP-seq:(Medium) rs1265370575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8554764,Human_RBP_ID_14561880 Human_Splice_Rec_465524,Human_Splice_Rec_465562,Human_Splice_Rec_465600,Human_Splice_Rec_465638,Human_Splice_Rec_465676 RMVar_hsa_circ_651,RMVar_hsa_circ_4024,RMVar_hsa_circ_220202,RMVar_hsa_circ_67617,RMVar_hsa_circ_20966,RMVar_hsa_circ_123676,RMVar_hsa_circ_220204,RMVar_hsa_circ_30177,RMVar_hsa_circ_83524,RMVar_hsa_circ_220206 77516 RMVar_ID_77516 Human_SNP_ID_147883142 m1A Human chr3 + 108581504 108581504 108581504 TCCTAGACAAGGCATTTTTAACTCATCTTCAGAAGATTGACTGTTGTTTTACATTGGTGTTTTGT TCCTAGACAAGGCATTTTTAACTCATCTTCAGGAGATTGACTGTTGTTTTACATTGGTGTTTTGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:108581489..108582186 32194978 MeRIP-seq:(Medium) rs777292363 Functional Loss SNV dbSNP153 33..33 33 - - - 77517 RMVar_ID_77517 Human_SNP_ID_147885198 m1A Human chr3 + 108589369 108589369 108589369 AGTCAGGAGCAAGGACTTCAAGCAGGCAGTGGAGTCCATTGCACCGGCCGCGGCCCGGCTTAGGG AGTCAGGAGCAAGGACTTCAAGCAGGCAGTGGGGTCCATTGCACCGGCCGCGGCCCGGCTTAGGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:108585735..108589425 32194978 MeRIP-seq:(Medium) rs756593907 Functional Loss SNV dbSNP153 33..33 33 - - - 77518 RMVar_ID_77518 Human_SNP_ID_147885226 m1A Human chr3 - 108589396 108589396 108589396 GGCCGGCGCACGCTGGGCGGTGGTGGTCCCTAAGCCGGGCCGCGGCCGGTGCAATGGACTCCACT GGCCGGCGCACGCTGGGCGGTGGTGGTCCCTACGCCGGGCCGCGGCCGGTGCAATGGACTCCACT T G CIP2A Ensembl:ENSG00000163507 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:108589317..108589417;chr3:108589319..108589406 26863196 MeRIP-seq:(Medium) rs1435661050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757376 RMVar_hsa_circ_76159,RMVar_hsa_circ_220211 77519 RMVar_ID_77519 Human_SNP_ID_148487000 m1A Human chr3 + 111071890 111071890 111071890 GCCAGCGTTCGGCCAAGTGTCAGCCGGCAGCGACGGCGCTAGAGCTGGGAGCTGGGGACGCGCGC GCCAGCGTTCGGCCAAGTGTCAGCCGGCAGCGGCGGCGCTAGAGCTGGGAGCTGGGGACGCGCGC A G NECTIN3 Ensembl:ENSG00000177707 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:111071770..111072122 26863196 MeRIP-seq:(Medium) rs1026796749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158893,Human_RBP_ID_4756633,Human_RBP_ID_5473556,Human_RBP_ID_18471808,Human_RBP_ID_22456079 77520 RMVar_ID_77520 Human_SNP_ID_148487116 m1A Human chr3 + 111072071 111072071 111072071 TCCCCGCTGTGTCCTGGAGGCGGCAAAGCACAACTTTCCTCCGCTTCTCTCCTCGGAGCCGGGCT TCCCCGCTGTGTCCTGGAGGCGGCAAAGCACAGCTTTCCTCCGCTTCTCTCCTCGGAGCCGGGCT A G NECTIN3 Ensembl:ENSG00000177707 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:111072020..111072190 26863196 MeRIP-seq:(Medium) rs1374059306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158893,Human_RBP_ID_4758247,Human_RBP_ID_5505244,Human_RBP_ID_9435423,Human_RBP_ID_27042653 77521 RMVar_ID_77521 Human_SNP_ID_148489749 m1A Human chr3 + 111082093 111082090 111082093 CAAAGGGATTTGAAGGGAGGCTTGGATCTGAGAAGTAGATGATATGGTGTTTGGATATCATTGTG CAAAGGGATTTGAAGGGAGGCTTGGATCTG___AGTAGATGATATGGTGTTTGGATATCATTGTG GAGA G NECTIN3 Ensembl:ENSG00000177707 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:111082088..111082202 26863196 MeRIP-seq:(Medium) rs1227593923 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_220243,RMVar_hsa_circ_106169,RMVar_hsa_circ_95920,RMVar_hsa_circ_220244,RMVar_hsa_circ_220242 77522 RMVar_ID_77522 Human_SNP_ID_148632589 m1A Human chr3 - 111674745 111674745 111674745 TGCCTGCTACTCACTCCCCCGCTTCTCTGCACAGACGCCCCCTGCCCTGTGGCTTCCTGAAAGAC TGCCTGCTACTCACTCCCCCGCTTCTCTGCACGGACGCCCCCTGCCCTGTGGCTTCCTGAAAGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:111674695..111674884 26863196 MeRIP-seq:(Medium) rs563880202 Functional Loss SNV dbSNP153 33..33 33 - - - 77523 RMVar_ID_77523 Human_SNP_ID_148674792 m1A Human chr3 - 111859859 111859859 111859859 GGAGCCCACTCACCGTCTCATCTTTCCTCCAAACCGCCGCTCTACGCTGGCGCCGCCGCCCTAGC GGAGCCCACTCACCGTCTCATCTTTCCTCCAACCCGCCGCTCTACGCTGGCGCCGCCGCCCTAGC T G AC117509.1 Ensembl:ENSG00000286492 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:111859696..111859893 26863196 MeRIP-seq:(Medium) rs1320490862 Functional Loss SNV dbSNP153 33..33 33 - - - 77524 RMVar_ID_77524 Human_SNP_ID_148674798 m1A Human chr3 + 111859871 111859871 111859871 GCGCCAGCGTAGAGCGGCGGTTTGGAGGAAAGATGAGACGGTGAGTGGGCTCCGGGGACACAGAG GCGCCAGCGTAGAGCGGCGGTTTGGAGGAAAGCTGAGACGGTGAGTGGGCTCCGGGGACACAGAG A C PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:111859655..111860005;chr3:111859743..111859883 26863196 MeRIP-seq:(Medium) rs1164260767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_466637,Human_Splice_Rec_466639,Human_Splice_Rec_466643 RMVar_hsa_circ_66165,RMVar_hsa_circ_365616 77525 RMVar_ID_77525 Human_SNP_ID_148674799 m1A Human chr3 - 111859872 111859872 111859872 ACTCTGTGTCCCCGGAGCCCACTCACCGTCTCATCTTTCCTCCAAACCGCCGCTCTACGCTGGCG ACTCTGTGTCCCCGGAGCCCACTCACCGTCTCGTCTTTCCTCCAAACCGCCGCTCTACGCTGGCG T C AC117509.1 Ensembl:ENSG00000286492 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:111859604..111860011 26863196 MeRIP-seq:(Medium) rs1336014899 Functional Loss SNV dbSNP153 33..33 33 - - - 77526 RMVar_ID_77526 Human_SNP_ID_148844250 m1A Human chr3 - 112561614 112561614 112561614 CTGCCAGCCGGGTGCTGATGCGAGTCGGTGGCAGCGAGGACATTTTCTGACTCCCTGGCCCCTGA CTGCCAGCCGGGTGCTGATGCGAGTCGGTGGCGGCGAGGACATTTTCTGACTCCCTGGCCCCTGA T C ATG3 Ensembl:ENSG00000144848 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:112561563..112562045 26863196 MeRIP-seq:(Medium) rs1387203523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_585686,Human_RBP_ID_1615491,Human_RBP_ID_4758251,Human_RBP_ID_5424775,Human_RBP_ID_5446847,Human_RBP_ID_14565461,Human_RBP_ID_27042748 RMVar_hsa_circ_115532,RMVar_hsa_circ_220293,RMVar_hsa_circ_90620,RMVar_hsa_circ_220300 77527 RMVar_ID_77527 Human_SNP_ID_148855728 m1A Human chr3 - 112605523 112605523 112605523 TCAGCAGTCACTGGGGATGCGCTGCCCAGAAGATGAGTATGCAGGCTATGGTTACCATAGTTACC TCAGCAGTCACTGGGGATGCGCTGCCCAGAAGTTGAGTATGCAGGCTATGGTTACCATAGTTACC T A CCDC80 Ensembl:ENSG00000091986 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:112605473..112605574 32194978 MeRIP-seq:(Medium) rs1329278792 Functional Loss SNV dbSNP153 33..33 33 - - - 77528 RMVar_ID_77528 Human_SNP_ID_148861613 m1A Human chr3 + 112630151 112630151 112630151 GAAAGTGGTCGATTTTCATGGTGCTGTTGTTGACAGGGCCGAAGATGGTGATCACAGAGATTTTC GAAAGTGGTCGATTTTCATGGTGCTGTTGTTGTCAGGGCCGAAGATGGTGATCACAGAGATTTTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:112619092..112630251 32194978 MeRIP-seq:(Medium) rs73214205 Functional Loss SNV dbSNP153 33..33 33 - - - 77529 RMVar_ID_77529 Human_SNP_ID_148863430 m1A Human chr3 - 112638156 112638156 112638156 AGAAAAAGAGCAAGCAAGAGAAAGAGAAGAGCAAGAAGAAAAAAGGAGGTAAAACAGAACAGGAT AGAAAAAGAGCAAGCAAGAGAAAGAGAAGAGCGAGAAGAAAAAAGGAGGTAAAACAGAACAGGAT T C CCDC80 Ensembl:ENSG00000091986 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:112638070..112638275 26863196 MeRIP-seq:(Medium) rs1426242203 Functional Loss SNV dbSNP153 33..33 33 - - - 77530 RMVar_ID_77530 Human_SNP_ID_148863574 m1A Human chr3 + 112638557 112638557 112638557 CTGGGCCAGCAGCCCTTGTGCTGGGTTCTGAGATGGTGGTGGGAGGGGCATTTGTGAAGCTCTCC CTGGGCCAGCAGCCCTTGTGCTGGGTTCTGAGGTGGTGGTGGGAGGGGCATTTGTGAAGCTCTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:112638506..112638607 32194978 MeRIP-seq:(Medium) rs1347036565 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 77531 RMVar_ID_77531 Human_SNP_ID_148863746 m1A Human chr3 - 112638970 112638969 112638970 GGAAGGCCAAGCCTGGGCAGCGAGAAGAAGAAAGAGGACCCAAGGAGAGCACAAGTCCCACCAAC GGAAGGCCAAGCCTGGGCAGCGAGAAGAAGAA_GAGGACCCAAGGAGAGCACAAGTCCCACCAAC CT C CCDC80 Ensembl:ENSG00000091986 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:112638740..112639172 26863196 MeRIP-seq:(Medium) rs943717173 Functional Loss DEL dbSNP153 33..33 33 - - - 77532 RMVar_ID_77532 Human_SNP_ID_148864380 m1A Human chr3 + 112640982 112640982 112640982 TTTTCTTCTTTCTCTTGCCTGGATTCAGTCCCAGAAATGTTAGGACTACCTCAGTTTTGCTCCAA TTTTCTTCTTTCTCTTGCCTGGATTCAGTCCCCGAAATGTTAGGACTACCTCAGTTTTGCTCCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:112640825..112641046;chr3:112640813..112641030 26863196 MeRIP-seq:(Medium) rs1237397621 Functional Loss SNV dbSNP153 33..33 33 - - - 77533 RMVar_ID_77533 Human_SNP_ID_148952103 m1A Human chr3 - 113019610 113019610 113019610 GGCTGCGGTGCCGCCGGGCCTGGAGCCGTGGAACCGTGTGAGAATCCCTAAGGCGGGGAACCGCA GGCTGCGGTGCCGCCGGGCCTGGAGCCGTGGAGCCGTGTGAGAATCCCTAAGGCGGGGAACCGCA T C NEPRO Ensembl:ENSG00000163608 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:113019492..113019640 26863196 MeRIP-seq:(Medium) rs751611625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248414,Human_RBP_ID_4716902,Human_RBP_ID_8555096,Human_RBP_ID_18424033 Human_Splice_Rec_467805,Human_Splice_Rec_467821,Human_Splice_Rec_467833,Human_Splice_Rec_467847,Human_Splice_Rec_467861,Human_Splice_Rec_467869,Human_Splice_Rec_467873,Human_Splice_Rec_467887,Human_Splice_Rec_467901,Human_Splice_Rec_467911,Human_Splice_Rec_467925,Human_Splice_Rec_467947,Human_Splice_Rec_467955,Human_Splice_Rec_467963,Human_Splice_Rec_467967,Human_Splice_Rec_467971,Human_Splice_Rec_467979,Human_Splice_Rec_467985,Human_Splice_Rec_467991 77534 RMVar_ID_77534 Human_SNP_ID_148998118 m1A Human chr3 + 113212237 113212237 113212237 CGAGGCTGGGCGCGCCGGGCGCCGGGCGAAGAAGTTGGGGCGAGGCGGGCAGCGGGGGTCCCGGG CGAGGCTGGGCGCGCCGGGCGCCGGGCGAAGAGGTTGGGGCGAGGCGGGCAGCGGGGGTCCCGGG A G BOC Ensembl:ENSG00000144857 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:113212102..113212371 26863196 MeRIP-seq:(Medium) rs1302076894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4716935 77535 RMVar_ID_77535 Human_SNP_ID_149037883 m1A Human chr3 - 113379508 113379508 113379508 AATTGAAAAGAGGGAGAGACAAAGGGAGTTGAAGGAGAAAATAAGGGAAGAAAGGAGGAACAAGC AATTGAAAAGAGGGAGAGACAAAGGGAGTTGAGGGAGAAAATAAGGGAAGAAAGGAGGAACAAGC T C AC112128.1,CFAP44 Ensembl:ENSG00000285943,Ensembl:ENSG00000206530 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:113379392..113379519 26863196 MeRIP-seq:(Medium) rs1287856780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2733224 Human_Splice_Rec_468306,Human_Splice_Rec_468400,Human_Splice_Rec_468436,Human_Splice_Rec_468538 RMVar_hsa_circ_26968,RMVar_hsa_circ_54588,RMVar_hsa_circ_64270,RMVar_hsa_circ_54740,RMVar_hsa_circ_58011,RMVar_hsa_circ_73770,RMVar_hsa_circ_367192,RMVar_hsa_circ_55815,RMVar_hsa_circ_357973,RMVar_hsa_circ_366459,RMVar_hsa_circ_283390,RMVar_hsa_circ_65354,RMVar_hsa_circ_123302,RMVar_hsa_circ_265573,RMVar_hsa_circ_353018,RMVar_hsa_circ_220316,RMVar_hsa_circ_69259 77536 RMVar_ID_77536 Human_SNP_ID_149054347 m1A Human chr3 - 113451872 113451872 113451872 GTTAGGGTGAGGTGAGTCATAGGGTAAGGGCCATCTCTGTCAGCACTGGGTCATGGGGAATAAGG GTTAGGGTGAGGTGAGTCATAGGGTAAGGGCCGTCTCTGTCAGCACTGGGTCATGGGGAATAAGG T C AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:113451753..113451953 26863196 MeRIP-seq:(Medium) rs1401814139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14566726 RMVar_hsa_circ_91470,RMVar_hsa_circ_220323,RMVar_hsa_circ_264790,RMVar_hsa_circ_39109,RMVar_hsa_circ_64525,RMVar_hsa_circ_220324 77537 RMVar_ID_77537 Human_SNP_ID_149054814 m1A Human chr3 - 113453701 113453701 113453701 ACAGCCCCTCTGCAATTCCCATTCCAACACTCAACAGTCAAGAAGCCCCACATTCTCAGAAGAGC ACAGCCCCTCTGCAATTCCCATTCCAACACTCGACAGTCAAGAAGCCCCACATTCTCAGAAGAGC T C AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs145510382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8120192,Human_RBP_ID_9393923,Human_RBP_ID_17287701,Human_RBP_ID_17401109,Human_RBP_ID_17991198,Human_RBP_ID_27042848 Human_miRNA_ID_1794544,Human_miRNA_ID_2296988 RMVar_hsa_circ_5064,RMVar_hsa_circ_91470,RMVar_hsa_circ_220323,RMVar_hsa_circ_264790,RMVar_hsa_circ_39109,RMVar_hsa_circ_64525,RMVar_hsa_circ_220324,RMVar_hsa_circ_356254,RMVar_hsa_circ_359996,RMVar_hsa_circ_33696 77538 RMVar_ID_77538 Human_SNP_ID_149054815 m1A Human chr3 - 113453701 113453701 113453701 ACAGCCCCTCTGCAATTCCCATTCCAACACTCAACAGTCAAGAAGCCCCACATTCTCAGAAGAGC ACAGCCCCTCTGCAATTCCCATTCCAACACTCCACAGTCAAGAAGCCCCACATTCTCAGAAGAGC T G AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs145510382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8120192,Human_RBP_ID_9393923,Human_RBP_ID_17287701,Human_RBP_ID_17401109,Human_RBP_ID_17991198,Human_RBP_ID_27042848 Human_miRNA_ID_1794544,Human_miRNA_ID_2296988 RMVar_hsa_circ_5064,RMVar_hsa_circ_91470,RMVar_hsa_circ_220323,RMVar_hsa_circ_264790,RMVar_hsa_circ_39109,RMVar_hsa_circ_64525,RMVar_hsa_circ_220324,RMVar_hsa_circ_356254,RMVar_hsa_circ_359996,RMVar_hsa_circ_33696 77539 RMVar_ID_77539 Human_SNP_ID_149064426 m1A Human chr3 - 113489391 113489391 113489391 GCAAAGTTGCAGGGCATAGGTGGTGAGTGAGGAGGGTGGAACAACTCTTTCAAGAAGTTTGGTGG GCAAAGTTGCAGGGCATAGGTGGTGAGTGAGGGGGGTGGAACAACTCTTTCAAGAAGTTTGGTGG T C AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:113489351..113489527 26863196 MeRIP-seq:(Medium) rs1319665455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23959639 RMVar_hsa_circ_5064,RMVar_hsa_circ_64525,RMVar_hsa_circ_33696,RMVar_hsa_circ_63075,RMVar_hsa_circ_40568,RMVar_hsa_circ_62995,RMVar_hsa_circ_364674,RMVar_hsa_circ_43525,RMVar_hsa_circ_220325,RMVar_hsa_circ_286475,RMVar_hsa_circ_287911,RMVar_hsa_circ_85718,RMVar_hsa_circ_220326,RMVar_hsa_circ_220327 77540 RMVar_ID_77540 Human_SNP_ID_149064751 m1A Human chr3 + 113490945 113490945 113490945 CATGGCTTTGGGTCAGGCCCTCACCACTTCTAAGATGCCCACCTAAGTCTTCTAACCAGACCCTC CATGGCTTTGGGTCAGGCCCTCACCACTTCTAGGATGCCCACCTAAGTCTTCTAACCAGACCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:113490769..113491114 26863196 MeRIP-seq:(Medium) rs182556757 Functional Loss SNV dbSNP153 33..33 33 - - - 77541 RMVar_ID_77541 Human_SNP_ID_149070287 m1A Human chr3 - 113515098 113515098 113515098 GCGCCTGAAGTTTTAGCTGCGGTGGCGGCGGCAGTCGGGACCGACTGCAAGGCAGGTTGAGATGA GCGCCTGAAGTTTTAGCTGCGGTGGCGGCGGCCGTCGGGACCGACTGCAAGGCAGGTTGAGATGA T G AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:113515007..113515113 26863196 MeRIP-seq:(Medium) rs1273911063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530609,Human_RBP_ID_18424276 77542 RMVar_ID_77542 Human_SNP_ID_149099277 m1A Human chr3 + 113632719 113632719 113632719 ACGTCAGTGAACAAAATGCCGGGCGCGGTGGCACGTGCCTGTAGTCCCAGCTACTTGGGAGGCTG ACGTCAGTGAACAAAATGCCGGGCGCGGTGGCTCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTG A T RN7SL767P Ensembl:ENSG00000241529 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1392075994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3134963 77543 RMVar_ID_77543 Human_SNP_ID_149120607 m1A Human chr3 - 113719653 113719653 113719653 GAATTGAGTGTGTAGGCTCCCTATCATTATATATAGAGTTTCTTTTTCCACGGTAGTCAGTGACT GAATTGAGTGTGTAGGCTCCCTATCATTATATGTAGAGTTTCTTTTTCCACGGTAGTCAGTGACT T C NAA50 Ensembl:ENSG00000121579 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:113719602..113719702 32194978 MeRIP-seq:(Medium) rs1042165401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_585989,Human_RBP_ID_3681702,Human_RBP_ID_4717061,Human_RBP_ID_7104203,Human_RBP_ID_8866795,Human_RBP_ID_9129514,Human_RBP_ID_10060745,Human_RBP_ID_14568263,Human_RBP_ID_17193992,Human_RBP_ID_17401142,Human_RBP_ID_17702519,Human_RBP_ID_17991293,Human_RBP_ID_21898283,Human_RBP_ID_23959862,Human_RBP_ID_24495039,Human_RBP_ID_26502220 77544 RMVar_ID_77544 Human_SNP_ID_149121081 m1A Human chr3 - 113721734 113721734 113721734 CAACTGAACAAATTACAAATGAACTTTCTTGCACTTGCTTGTCGCCAAATAAAAGAGAGGCCCAT CAACTGAACAAATTACAAATGAACTTTCTTGCGCTTGCTTGTCGCCAAATAAAAGAGAGGCCCAT T C NAA50 Ensembl:ENSG00000121579 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:113721651..113721777 26863196 MeRIP-seq:(Medium) rs1344612847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_586062,Human_RBP_ID_1383346,Human_RBP_ID_1615609,Human_RBP_ID_1946402,Human_RBP_ID_2733444,Human_RBP_ID_3681721,Human_RBP_ID_7104313,Human_RBP_ID_8555273,Human_RBP_ID_8866843,Human_RBP_ID_9129537,Human_RBP_ID_14568386,Human_RBP_ID_18793979,Human_RBP_ID_23959907,Human_RBP_ID_26824036,Human_RBP_ID_27311736 Human_Splice_Rec_468888,Human_Splice_Rec_468916 Human_miRNA_ID_213563,Human_miRNA_ID_223097,Human_miRNA_ID_517553,Human_miRNA_ID_521782,Human_miRNA_ID_761614,Human_miRNA_ID_766526,Human_miRNA_ID_771394,Human_miRNA_ID_776255,Human_miRNA_ID_781107,Human_miRNA_ID_785963,Human_miRNA_ID_790791,Human_miRNA_ID_1073088,Human_miRNA_ID_1107280,Human_miRNA_ID_1112107,Human_miRNA_ID_1259444,Human_miRNA_ID_1326110,Human_miRNA_ID_1568159,Human_miRNA_ID_1573843,Human_miRNA_ID_1581005,Human_miRNA_ID_1600476,Human_miRNA_ID_1609928,Human_miRNA_ID_1614848,Human_miRNA_ID_1622331,Human_miRNA_ID_1638445 77545 RMVar_ID_77545 Human_SNP_ID_149127272 m1A Human chr3 - 113746027 113746027 113746027 AGGCCGGCTTGCGGGGTTGAGTGGCCCGAGCTAAGGGTGCGGAGACCTAAGGGCGGCGACTACGA AGGCCGGCTTGCGGGGTTGAGTGGCCCGAGCTGAGGGTGCGGAGACCTAAGGGCGGCGACTACGA T C NAA50 Ensembl:ENSG00000121579 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:113745976..113746150 32194978 MeRIP-seq:(Medium) rs1204052625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69841,Human_RBP_ID_248250,Human_RBP_ID_586077,Human_RBP_ID_1030384,Human_RBP_ID_1615662,Human_RBP_ID_4717168,Human_RBP_ID_5424796,Human_RBP_ID_5474807,Human_RBP_ID_7104575,Human_RBP_ID_8555337,Human_RBP_ID_8866855,Human_RBP_ID_9393928,Human_RBP_ID_14569488,Human_RBP_ID_22456082,Human_RBP_ID_23960000,Human_RBP_ID_27042982 Human_Splice_Rec_468863,Human_Splice_Rec_468871,Human_Splice_Rec_468873,Human_Splice_Rec_468885,Human_Splice_Rec_468897,Human_Splice_Rec_468905,Human_Splice_Rec_468917,Human_Splice_Rec_468921 77546 RMVar_ID_77546 Human_SNP_ID_149127291 m1A Human chr3 + 113746076 113746076 113746076 CCCCGCAAGCCGGCCTCCTAGCCTGGGCAGGGAGCTGTGCGAGCAACGAAGGCCGCGAGAGTCGA CCCCGCAAGCCGGCCTCCTAGCCTGGGCAGGGTGCTGTGCGAGCAACGAAGGCCGCGAGAGTCGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:113746001..113746250 26863196 MeRIP-seq:(Medium) rs1261517016 Functional Loss SNV dbSNP153 33..33 33 - - - 77547 RMVar_ID_77547 Human_SNP_ID_149127305 m1A Human chr3 - 113746127 113746127 113746127 CAAGCGCGGCGGCGGGAGACACTCCCGCCCCCACCAGACTCAAGCCCTCACTCGACTCTCGCGGC CAAGCGCGGCGGCGGGAGACACTCCCGCCCCCGCCAGACTCAAGCCCTCACTCGACTCTCGCGGC T C NAA50 Ensembl:ENSG00000121579 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:113746026..113746250 26863196 MeRIP-seq:(Medium) rs1416722629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4717175,Human_RBP_ID_9393929,Human_RBP_ID_22456082,Human_RBP_ID_27042984 77548 RMVar_ID_77548 Human_SNP_ID_149127311 m1A Human chr3 - 113746139 113746139 113746139 GAAGCGGCGGCACAAGCGCGGCGGCGGGAGACACTCCCGCCCCCACCAGACTCAAGCCCTCACTC GAAGCGGCGGCACAAGCGCGGCGGCGGGAGACGCTCCCGCCCCCACCAGACTCAAGCCCTCACTC T C NAA50 Ensembl:ENSG00000121579 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:113746085..113746201 26863410 MeRIP-seq:(Medium) rs370119217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4717175,Human_RBP_ID_22456082 77549 RMVar_ID_77549 Human_SNP_ID_149127312 m1A Human chr3 - 113746139 113746139 113746139 GAAGCGGCGGCACAAGCGCGGCGGCGGGAGACACTCCCGCCCCCACCAGACTCAAGCCCTCACTC GAAGCGGCGGCACAAGCGCGGCGGCGGGAGACCCTCCCGCCCCCACCAGACTCAAGCCCTCACTC T G NAA50 Ensembl:ENSG00000121579 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:113746085..113746201 26863410 MeRIP-seq:(Medium) rs370119217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4717175,Human_RBP_ID_22456082 77550 RMVar_ID_77550 Human_SNP_ID_149127753 m1A Human chr3 - 113747115 113747115 113747115 CCCCACCACTCGCCAGTTACCGGTCGCCGCTCACCTGCTGGGGCGCGAGGTGCAGAGACTGTACC CCCCACCACTCGCCAGTTACCGGTCGCCGCTCCCCTGCTGGGGCGCGAGGTGCAGAGACTGTACC T G AC108693.2 Ensembl:ENSG00000242659 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:113747095..113747166 26863196 MeRIP-seq:(Medium) rs2712349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_468926 77551 RMVar_ID_77551 Human_SNP_ID_149150109 m1A Human chr3 - 113838929 113838929 113838929 TGCCCCAGCGAGGCCCGCGGCTTACCTGACGGACAGTCGGAGCGCCCTCCATCGCGGCTCCCTCC TGCCCCAGCGAGGCCCGCGGCTTACCTGACGGTCAGTCGGAGCGCCCTCCATCGCGGCTCCCTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:113838800..113838969 26863196 MeRIP-seq:(Medium) rs1283822422 Functional Loss SNV dbSNP153 33..33 33 - - - 77552 RMVar_ID_77552 Human_SNP_ID_149199327 m1A Human chr3 + 114056834 114056834 114056834 GTAGTGAACTGTGAGGAGTTTGAGGGGTCTGAAGACTGAAAGAGTCGAATGGTTTGTTGGCAGGT GTAGTGAACTGTGAGGAGTTTGAGGGGTCTGAGGACTGAAAGAGTCGAATGGTTTGTTGGCAGGT A G QTRT2 Ensembl:ENSG00000151576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:114056785..114056921 26863196 MeRIP-seq:(Medium) rs1397087639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_935707,Human_RBP_ID_1615720,Human_RBP_ID_1946591,Human_RBP_ID_3681912,Human_RBP_ID_7104988,Human_RBP_ID_18424036,Human_RBP_ID_19012831,Human_RBP_ID_23960287 Human_Splice_Rec_469391,Human_Splice_Rec_469405,Human_Splice_Rec_469421,Human_Splice_Rec_469427,Human_Splice_Rec_469429,Human_Splice_Rec_469441,Human_Splice_Rec_469449 77553 RMVar_ID_77553 Human_SNP_ID_149337655 m1A Human chr3 - 114655166 114655166 114655166 AAAAATCAAAAGCATATAATGAAATAAATGGTAGACCTAAACTTAATTGTAGCAATAATTCCATT AAAAATCAAAAGCATATAATGAAATAAATGGTTGACCTAAACTTAATTGTAGCAATAATTCCATT T A ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:114655150..114655237 26863410 MeRIP-seq:(Medium) rs1455807050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86426,RMVar_hsa_circ_15083,RMVar_hsa_circ_101902,RMVar_hsa_circ_29125,RMVar_hsa_circ_61212,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_19544,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_93489,RMVar_hsa_circ_20050,RMVar_hsa_circ_60221,RMVar_hsa_circ_220392,RMVar_hsa_circ_63551,RMVar_hsa_circ_365618,RMVar_hsa_circ_54355 77554 RMVar_ID_77554 Human_SNP_ID_149384648 m1A Human chr3 - 114859270 114859259 114859271 AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAGAATGGAAGGAAGGAGGAAAAGAAAGAAGAAAGGA AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAG____________GAGGAAAAGAAAGAAGAAAGGA CCTTCCTTCCATT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:114859220..114859299 26863196 MeRIP-seq:(Medium) rs1162827510 Functional Loss DEL dbSNP153 32..43 33 - - - RMVar_hsa_circ_86426,RMVar_hsa_circ_101902,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_20050,RMVar_hsa_circ_54355,RMVar_hsa_circ_21605,RMVar_hsa_circ_61207,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_353408,RMVar_hsa_circ_220398 77555 RMVar_ID_77555 Human_SNP_ID_149384649 m1A Human chr3 - 114859270 114859263 114859271 AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAGAATGGAAGGAAGGAGGAAAAGAAAGAAGAAAGGA AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAG________GAAGGAGGAAAAGAAAGAAGAAAGGA CCTTCCATT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:114859220..114859299 26863196 MeRIP-seq:(Medium) rs1438679245 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_86426,RMVar_hsa_circ_101902,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_20050,RMVar_hsa_circ_54355,RMVar_hsa_circ_21605,RMVar_hsa_circ_61207,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_353408,RMVar_hsa_circ_220398 77556 RMVar_ID_77556 Human_SNP_ID_149384652 m1A Human chr3 - 114859270 114859267 114859271 AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAGAATGGAAGGAAGGAGGAAAAGAAAGAAGAAAGGA AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAG____GAAGGAAGGAGGAAAAGAAAGAAGAAAGGA CCATT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:114859220..114859299 26863196 MeRIP-seq:(Medium) rs138462352 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_86426,RMVar_hsa_circ_101902,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_20050,RMVar_hsa_circ_54355,RMVar_hsa_circ_21605,RMVar_hsa_circ_61207,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_353408,RMVar_hsa_circ_220398 77557 RMVar_ID_77557 Human_SNP_ID_149401413 m1A Human chr3 - 114934306 114934304 114934307 GATTTGAGGAATCGTGGGCAGCAAAGTAAAGAAGGCTTTCCTGAAGAGGTCGCAGGTAAGTGGAG GATTTGAGGAATCGTGGGCAGCAAAGTAAAG___GCTTTCCTGAAGAGGTCGCAGGTAAGTGGAG CCTT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:114934260..114934408 26863196 MeRIP-seq:(Medium) rs952853222 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_13753,RMVar_hsa_circ_86426,RMVar_hsa_circ_99266,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_21605,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_317091 77558 RMVar_ID_77558 Human_SNP_ID_149401416 m1A Human chr3 - 114934306 114934306 114934306 GATTTGAGGAATCGTGGGCAGCAAAGTAAAGAAGGCTTTCCTGAAGAGGTCGCAGGTAAGTGGAG GATTTGAGGAATCGTGGGCAGCAAAGTAAAGACGGCTTTCCTGAAGAGGTCGCAGGTAAGTGGAG T G ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:114934260..114934408 26863196 MeRIP-seq:(Medium) rs965400546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13753,RMVar_hsa_circ_86426,RMVar_hsa_circ_99266,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_21605,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_317091 77559 RMVar_ID_77559 Human_SNP_ID_149449071 m1A Human chr3 - 115146764 115146764 115146764 AGGGGGACTAGCCGGGGCTCAGGAGCTGCTAGAGGCGCCCGCTTGTCTTCTGCCCCCTCCCTCCT AGGGGGACTAGCCGGGGCTCAGGAGCTGCTAGGGGCGCCCGCTTGTCTTCTGCCCCCTCCCTCCT T C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:115146735..115146837 26863196 MeRIP-seq:(Medium) rs1288484509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721433 77560 RMVar_ID_77560 Human_SNP_ID_149449356 m1A Human chr3 - 115147229 115147229 115147229 GAAGTTTAGGAGTTGAGGAAAGAAGATTAAAGAGCGCGAGGAGGTAATGCCACAAACTCTAATTT GAAGTTTAGGAGTTGAGGAAAGAAGATTAAAGGGCGCGAGGAGGTAATGCCACAAACTCTAATTT T C ZBTB20 Ensembl:ENSG00000181722 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:115147117..115147241 26863196 MeRIP-seq:(Medium) rs892215094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424037 Human_Splice_Rec_469587,Human_Splice_Rec_469779 77561 RMVar_ID_77561 Human_SNP_ID_150455184 m1A Human chr3 + 119240044 119240044 119240044 AAGCCACAACTCGCCTCCACGCTCAGATTACCATTTTCTTTTTCCTCCTTTTCATCACCAAACGG AAGCCACAACTCGCCTCCACGCTCAGATTACCCTTTTCTTTTTCCTCCTTTTCATCACCAAACGG A C B4GALT4-AS1 Ensembl:ENSG00000240254 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:119240030..119240190 26863196 MeRIP-seq:(Medium) rs79146935 Functional Loss SNV dbSNP153 33..33 33 - - - 77562 RMVar_ID_77562 Human_SNP_ID_150455185 m1A Human chr3 + 119240044 119240044 119240044 AAGCCACAACTCGCCTCCACGCTCAGATTACCATTTTCTTTTTCCTCCTTTTCATCACCAAACGG AAGCCACAACTCGCCTCCACGCTCAGATTACCGTTTTCTTTTTCCTCCTTTTCATCACCAAACGG A G B4GALT4-AS1 Ensembl:ENSG00000240254 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:119240030..119240190 26863196 MeRIP-seq:(Medium) rs79146935 Functional Loss SNV dbSNP153 33..33 33 - - - 77563 RMVar_ID_77563 Human_SNP_ID_150455417 m1A Human chr3 - 119240729 119240729 119240729 AGTCCCAGGGCTGTAGCGGGGCGGGCGTGGGGATGACGTGGCGGCGTCCGTGGGGCAGTCCCGCC AGTCCCAGGGCTGTAGCGGGGCGGGCGTGGGGGTGACGTGGCGGCGTCCGTGGGGCAGTCCCGCC T C B4GALT4 Ensembl:ENSG00000121578 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:119240685..119240830 26863196 MeRIP-seq:(Medium) rs1446430411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5392061,Human_RBP_ID_18424279 77564 RMVar_ID_77564 Human_SNP_ID_150501153 m1A Human chr3 - 119434855 119434855 119434855 CTTAGTTGGTCAGAAAATACAATATGGCCTCAAGGGGTGCTGGTGCGGCACAGCAGATGTTTATA CTTAGTTGGTCAGAAAATACAATATGGCCTCAGGGGGTGCTGGTGCGGCACAGCAGATGTTTATA T C TMEM39A Ensembl:ENSG00000176142 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:119432190..119435759 32194978 MeRIP-seq:(Medium) rs1437327013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933264,Human_RBP_ID_3682500,Human_RBP_ID_7107633,Human_RBP_ID_17991919,Human_RBP_ID_18445851,Human_RBP_ID_22676592,Human_RBP_ID_22745005,Human_RBP_ID_22768920,Human_RBP_ID_25764714 Human_Splice_Rec_470702,Human_Splice_Rec_470706,Human_Splice_Rec_470722 RMVar_hsa_circ_12984,RMVar_hsa_circ_18007 77565 RMVar_ID_77565 Human_SNP_ID_150501154 m1A Human chr3 - 119434855 119434855 119434855 CTTAGTTGGTCAGAAAATACAATATGGCCTCAAGGGGTGCTGGTGCGGCACAGCAGATGTTTATA CTTAGTTGGTCAGAAAATACAATATGGCCTCACGGGGTGCTGGTGCGGCACAGCAGATGTTTATA T G TMEM39A Ensembl:ENSG00000176142 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:119432190..119435759 32194978 MeRIP-seq:(Medium) rs1437327013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933264,Human_RBP_ID_3682500,Human_RBP_ID_7107633,Human_RBP_ID_17991919,Human_RBP_ID_18445851,Human_RBP_ID_22676592,Human_RBP_ID_22745005,Human_RBP_ID_22768920,Human_RBP_ID_25764714 Human_Splice_Rec_470702,Human_Splice_Rec_470706,Human_Splice_Rec_470722 RMVar_hsa_circ_12984,RMVar_hsa_circ_18007 77566 RMVar_ID_77566 Human_SNP_ID_150516557 m1A Human chr3 - 119498652 119498652 119498652 CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTACGAGGTGAGAATCCGTGCATTTGACCCAGGTT CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTGCGAGGTGAGAATCCGTGCATTTGACCCAGGTT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:119498570..119498663 26863410 MeRIP-seq:(Medium) rs994397031 Functional Loss SNV dbSNP153 33..33 33 - - - 77567 RMVar_ID_77567 Human_SNP_ID_150516558 m1A Human chr3 - 119498652 119498652 119498652 CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTACGAGGTGAGAATCCGTGCATTTGACCCAGGTT CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTCCGAGGTGAGAATCCGTGCATTTGACCCAGGTT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:119498570..119498663 26863410 MeRIP-seq:(Medium) rs994397031 Functional Loss SNV dbSNP153 33..33 33 - - - 77568 RMVar_ID_77568 Human_SNP_ID_150560613 m1A Human chr3 - 119677259 119677256 119677259 CAAACCCTGCCCCGCCTGAGTCTCAGGAGAAGAAGCCGCTGAAGCCCTGCTGCGCTTGCCCGGAG CAAACCCTGCCCCGCCTGAGTCTCAGGAGAAG___CCGCTGAAGCCCTGCTGCGCTTGCCCGGAG GCTT G COX17 Ensembl:ENSG00000138495 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:119677152..119677338 26863196 MeRIP-seq:(Medium) rs776316905 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_586629,Human_RBP_ID_4757391,Human_RBP_ID_5120583,Human_RBP_ID_23962740,Human_RBP_ID_26824041 Human_Splice_Rec_471157,Human_Splice_Rec_471163,Human_Splice_Rec_471167,Human_Splice_Rec_471173,Human_Splice_Rec_471181 77569 RMVar_ID_77569 Human_SNP_ID_150560615 m1A Human chr3 - 119677259 119677259 119677259 CAAACCCTGCCCCGCCTGAGTCTCAGGAGAAGAAGCCGCTGAAGCCCTGCTGCGCTTGCCCGGAG CAAACCCTGCCCCGCCTGAGTCTCAGGAGAAGCAGCCGCTGAAGCCCTGCTGCGCTTGCCCGGAG T G COX17 Ensembl:ENSG00000138495 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:119677152..119677338 26863196 MeRIP-seq:(Medium) rs1374049665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_586629,Human_RBP_ID_4757391,Human_RBP_ID_5120583,Human_RBP_ID_23962740,Human_RBP_ID_26824041 Human_Splice_Rec_471157,Human_Splice_Rec_471163,Human_Splice_Rec_471167,Human_Splice_Rec_471173,Human_Splice_Rec_471181 77570 RMVar_ID_77570 Human_SNP_ID_150560618 m1A Human chr3 + 119677269 119677269 119677269 GCGCAGCAGGGCTTCAGCGGCTTCTTCTCCTGAGACTCAGGCGGGGCAGGGTTTGAGTCAACCAG GCGCAGCAGGGCTTCAGCGGCTTCTTCTCCTGTGACTCAGGCGGGGCAGGGTTTGAGTCAACCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:119677164..119677405 26863196 MeRIP-seq:(Medium) rs1399804234 Functional Loss SNV dbSNP153 33..33 33 - - - 77571 RMVar_ID_77571 Human_SNP_ID_150560622 m1A Human chr3 + 119677275 119677275 119677275 CAGGGCTTCAGCGGCTTCTTCTCCTGAGACTCAGGCGGGGCAGGGTTTGAGTCAACCAGACCCGG CAGGGCTTCAGCGGCTTCTTCTCCTGAGACTCGGGCGGGGCAGGGTTTGAGTCAACCAGACCCGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:119677201..119677300 32194978 MeRIP-seq:(Medium) rs1314137115 Functional Loss SNV dbSNP153 33..33 33 - - - 77572 RMVar_ID_77572 Human_SNP_ID_150596361 m1A Human chr3 + 119824952 119824952 119824952 TAGGGCCTGCAGGAGGGCTGCCAACAGACTCCACTTCCGAACCCTCTGGAGGACGAGACCCATAA TAGGGCCTGCAGGAGGGCTGCCAACAGACTCCGCTTCCGAACCCTCTGGAGGACGAGACCCATAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:119824902..119825102 26863196 MeRIP-seq:(Medium) rs942923784 Functional Loss SNV dbSNP153 33..33 33 - - - 77573 RMVar_ID_77573 Human_SNP_ID_150631186 m1A Human chr3 - 119967759 119967759 119967759 AGAGAGAAAAGAAAGAGAAAGAAAAGAAAAGGAGGGGAGGGGAGGGGACGGGACGGGAGAAAGGA AGAGAGAAAAGAAAGAGAAAGAAAAGAAAAGGGGGGGAGGGGAGGGGACGGGACGGGAGAAAGGA T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:119967756..119967942 26863196 MeRIP-seq:(Medium) rs560031381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25689761 RMVar_hsa_circ_18437,RMVar_hsa_circ_62483,RMVar_hsa_circ_354613,RMVar_hsa_circ_347331,RMVar_hsa_circ_300390,RMVar_hsa_circ_377669,RMVar_hsa_circ_220516,RMVar_hsa_circ_220517,RMVar_hsa_circ_220519,RMVar_hsa_circ_310667 77574 RMVar_ID_77574 Human_SNP_ID_150631210 m1A Human chr3 - 119967805 119967805 119967805 AGAAAGAGAAAGAGAGAAAGGGAGGGAGGGAGAGAGGGAGAGAGAGAGAGAGAAAAGAAAGAGAA AGAAAGAGAAAGAGAGAAAGGGAGGGAGGGAGGGAGGGAGAGAGAGAGAGAGAAAAGAAAGAGAA T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:119967802..119967912 26863196 MeRIP-seq:(Medium) rs1291968935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18437,RMVar_hsa_circ_62483,RMVar_hsa_circ_354613,RMVar_hsa_circ_347331,RMVar_hsa_circ_300390,RMVar_hsa_circ_377669,RMVar_hsa_circ_220516,RMVar_hsa_circ_220517,RMVar_hsa_circ_220519,RMVar_hsa_circ_310667 77575 RMVar_ID_77575 Human_SNP_ID_150634123 m1A Human chr3 + 119979373 119979373 119979373 TCCTCCGAAACTCCTTTTGACCCTGCAGATGAACCCTCTCTGTATTCTTATCCCCCTGCATCTGC TCCTCCGAAACTCCTTTTGACCCTGCAGATGACCCCTCTCTGTATTCTTATCCCCCTGCATCTGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:119979372..119979483 26863196 MeRIP-seq:(Medium) rs1240713849 Functional Loss SNV dbSNP153 33..33 33 - - - 77576 RMVar_ID_77576 Human_SNP_ID_57822777 m1A Human chr2 + 238120 238120 238120 ATGATTGACTGCTGTCAGCCTTCAAGCCCCACATCTGGACAACCCGCTAAGAAAGCTGGGCTTCC ATGATTGACTGCTGTCAGCCTTCAAGCCCCACGTCTGGACAACCCGCTAAGAAAGCTGGGCTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238114..238233 26863196 MeRIP-seq:(Medium) rs1206216768 Functional Loss SNV dbSNP153 33..33 33 - - - 77577 RMVar_ID_77577 Human_SNP_ID_57822778 m1A Human chr2 + 238120 238120 238120 ATGATTGACTGCTGTCAGCCTTCAAGCCCCACATCTGGACAACCCGCTAAGAAAGCTGGGCTTCC ATGATTGACTGCTGTCAGCCTTCAAGCCCCACTTCTGGACAACCCGCTAAGAAAGCTGGGCTTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238114..238233 26863196 MeRIP-seq:(Medium) rs1206216768 Functional Loss SNV dbSNP153 33..33 33 - - - 77578 RMVar_ID_77578 Human_SNP_ID_57829764 m1A Human chr2 - 265001 265001 265001 ACATGAGTAAGTCGGCGCCCTCTTACCCAGACACACAAACAGCACGGACTTGGTAGCCTGTTCCG ACATGAGTAAGTCGGCGCCCTCTTACCCAGACGCACAAACAGCACGGACTTGGTAGCCTGTTCCG T C SH3YL1 Ensembl:ENSG00000035115 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:264951..265069;chr2:264951..265070 26863196 MeRIP-seq:(Medium) rs1160727073 Functional Loss SNV dbSNP153 33..33 33 - - - 77579 RMVar_ID_77579 Human_SNP_ID_57829769 m1A Human chr2 - 265005 265005 265005 CAGAACATGAGTAAGTCGGCGCCCTCTTACCCAGACACACAAACAGCACGGACTTGGTAGCCTGT CAGAACATGAGTAAGTCGGCGCCCTCTTACCCGGACACACAAACAGCACGGACTTGGTAGCCTGT T C SH3YL1 Ensembl:ENSG00000035115 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:264967..269335 32194978 MeRIP-seq:(Medium) rs765630438 Functional Loss SNV dbSNP153 33..33 33 - - - 77580 RMVar_ID_77580 Human_SNP_ID_57832381 m1A Human chr2 + 275171 275171 275171 GATTACCAAAGAAGATTTTGCCACATTTGATTATATACTATGTATGGATGAAAGCAATCTGAGGT GATTACCAAAGAAGATTTTGCCACATTTGATTGTATACTATGTATGGATGAAAGCAATCTGAGGT A G ACP1 Ensembl:ENSG00000143727 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:275144..275243 32194978 MeRIP-seq:(Medium) rs773162713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1914857,Human_RBP_ID_3621847,Human_RBP_ID_9105165,Human_RBP_ID_9347356,Human_RBP_ID_13841429,Human_RBP_ID_17965091,Human_RBP_ID_22815348,Human_RBP_ID_23865326,Human_RBP_ID_27694661 Human_Splice_Rec_209988,Human_Splice_Rec_209989,Human_Splice_Rec_210012,Human_Splice_Rec_210013,Human_Splice_Rec_210030,Human_Splice_Rec_210042,Human_Splice_Rec_210048,Human_Splice_Rec_210049,Human_Splice_Rec_210060,Human_Splice_Rec_210061,Human_Splice_Rec_210070,Human_Splice_Rec_210071,Human_Splice_Rec_210075 Human_miRNA_ID_1141493,Human_miRNA_ID_1212474 RMVar_hsa_circ_54400 77581 RMVar_ID_77581 Human_SNP_ID_57832914 m1A Human chr2 + 277339 277339 277339 CAGGTTCGTGCCCTGCTGCGGCCAGCCTGACTAGACCCCACCCTGAGGTCCTGCATTTCTCAGTC CAGGTTCGTGCCCTGCTGCGGCCAGCCTGACTGGACCCCACCCTGAGGTCCTGCATTTCTCAGTC A G ACP1 Ensembl:ENSG00000143727 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:277005..277400 32194978 MeRIP-seq:(Medium) rs1042064742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548866,Human_RBP_ID_1585670,Human_RBP_ID_6906602,Human_RBP_ID_13843782,Human_RBP_ID_17275838,Human_RBP_ID_17507074,Human_RBP_ID_17954949,Human_RBP_ID_20560094,Human_RBP_ID_22450983,Human_RBP_ID_23865623,Human_RBP_ID_27289407 Human_miRNA_ID_474543 77582 RMVar_ID_77582 Human_SNP_ID_57924354 m1A Human chr2 + 628874 628874 628874 TAGGACACAAGTCCCCAGGCAGGCTTGTTGGGACTCCAGCGAGGTAGCTTTTCCATCACTGAAGG TAGGACACAAGTCCCCAGGCAGGCTTGTTGGGTCTCCAGCGAGGTAGCTTTTCCATCACTGAAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:628862..628970 26863196 MeRIP-seq:(Medium) rs1325063154 Functional Loss SNV dbSNP153 33..33 33 - - - 77583 RMVar_ID_77583 Human_SNP_ID_57936663 m1A Human chr2 - 674923 674923 674923 GGAGGGCAGCAGCCCGACATGCAGAGACTGAGATAGATGGAAGGTGTGGATCAGAGGCAGAGAAA GGAGGGCAGCAGCCCGACATGCAGAGACTGAGGTAGATGGAAGGTGTGGATCAGAGGCAGAGAAA T C TMEM18 Ensembl:ENSG00000151353 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:674890..675026 26863196 MeRIP-seq:(Medium) rs760893072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6941878,Human_RBP_ID_13943034 RMVar_hsa_circ_102063,RMVar_hsa_circ_85936,RMVar_hsa_circ_196599,RMVar_hsa_circ_196600 77584 RMVar_ID_77584 Human_SNP_ID_57936860 m1A Human chr2 - 675632 675632 675632 AGGACAGTGAGTGTCTGCTGGTGTGTTCCTACAGCAGACGGACTGGACTGAGCCCTGGCTCATGG AGGACAGTGAGTGTCTGCTGGTGTGTTCCTACGGCAGACGGACTGGACTGAGCCCTGGCTCATGG T C TMEM18 Ensembl:ENSG00000151353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:675612..675682 26863196 MeRIP-seq:(Medium) rs899020789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553951,Human_RBP_ID_916120,Human_RBP_ID_4614122,Human_RBP_ID_5379024,Human_RBP_ID_13943055,Human_RBP_ID_22547003,Human_RBP_ID_23880991 77585 RMVar_ID_77585 Human_SNP_ID_57937076 m1A Human chr2 - 676234 676234 676234 AGGTCCCTGAGCCAGACACTGTCCCCAGGTACAGCAGGGTCCCGGGGAGTCCAGGAGGCGGCGGA AGGTCCCTGAGCCAGACACTGTCCCCAGGTACGGCAGGGTCCCGGGGAGTCCAGGAGGCGGCGGA T C TMEM18 Ensembl:ENSG00000151353 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:676188..676389 26863196 MeRIP-seq:(Medium) rs1192804193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639535,Human_RBP_ID_9330310 Human_Splice_Rec_210414,Human_Splice_Rec_210448,Human_Splice_Rec_210452 RMVar_hsa_circ_38380 77586 RMVar_ID_77586 Human_SNP_ID_57952803 m1A Human chr2 + 740015 740015 740015 AGGAAGGCAGCCAGGATCTTCCCTCAGAGCCTAGCGAGGGGGCGCGGCCCAGCCAGGAGAGCTGG AGGAAGGCAGCCAGGATCTTCCCTCAGAGCCTGGCGAGGGGGCGCGGCCCAGCCAGGAGAGCTGG A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:739929..740053 26863196 MeRIP-seq:(Medium) rs368695721 Functional Loss SNV dbSNP153 33..33 33 - - - 77587 RMVar_ID_77587 Human_SNP_ID_57952955 m1A Human chr2 + 740204 740204 740204 GGAGAGGCCCGGAGGATCTTCCCTCAGAGCCTAGCGAGGGAGCGCGGCCCAGCCAGGAGAGCTGG GGAGAGGCCCGGAGGATCTTCCCTCAGAGCCTGGCGAGGGAGCGCGGCCCAGCCAGGAGAGCTGG A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740169..740290 26863196 MeRIP-seq:(Medium) rs1194649331 Functional Loss SNV dbSNP153 33..33 33 - - - 77588 RMVar_ID_77588 Human_SNP_ID_57953244 m1A Human chr2 + 740672 740609 740672 AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG _________________________________GCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG GGCTGGAGAGGCAGCGAGGATCTTCCCTAAGAGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGA G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740596..741063 26863196 MeRIP-seq:(Medium) rs1558201625 Functional Loss DEL dbSNP153 1..33 33 - - - 77589 RMVar_ID_77589 Human_SNP_ID_57953290 m1A Human chr2 + 740672 740672 740672 AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGGGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740596..741063 26863196 MeRIP-seq:(Medium) rs113469378 Functional Loss SNV dbSNP153 33..33 33 - - - 77590 RMVar_ID_77590 Human_SNP_ID_57953291 m1A Human chr2 + 740672 740672 740672 AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGTGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG A T lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740596..741063 26863196 MeRIP-seq:(Medium) rs113469378 Functional Loss SNV dbSNP153 33..33 33 - - - 77591 RMVar_ID_77591 Human_SNP_ID_57953301 m1A Human chr2 + 740688 740688 740688 GTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAGCCTGGCGAGGGGGCGC GTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGGGGATCTTCCCTCAGAGCCTGGCGAGGGGGCGC A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr2:740577..740710;chr2:740455..741029 26863196 MeRIP-seq:(Medium) rs1258893765 Functional Loss SNV dbSNP153 33..33 33 - - - 77592 RMVar_ID_77592 Human_SNP_ID_57955106 m1A Human chr2 + 747936 747936 747936 TCACCATCACCACCACCAATGACAATGACATCACAGCCCCGACCTCACCATCACCACCACCAATG TCACCATCACCACCACCAATGACAATGACATCCCAGCCCCGACCTCACCATCACCACCACCAATG A C AC116609.2 Ensembl:ENSG00000231173 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:747721..748184 26863196 MeRIP-seq:(Medium) rs376461937 Functional Loss SNV dbSNP153 33..33 33 - - - 77593 RMVar_ID_77593 Human_SNP_ID_57955117 m1A Human chr2 + 747962 747962 747962 GACATCACAGCCCCGACCTCACCATCACCACCACCAATGACGATGCTACAGCCCCGACCTCACCA GACATCACAGCCCCGACCTCACCATCACCACCGCCAATGACGATGCTACAGCCCCGACCTCACCA A G AC116609.2 Ensembl:ENSG00000231173 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:747914..747999 26863196 MeRIP-seq:(Medium) rs1481454928 Functional Loss SNV dbSNP153 33..33 33 - - - 77594 RMVar_ID_77594 Human_SNP_ID_58152598 m1A Human chr2 - 1480801 1480773 1480802 AGCAGCAGGGACGTGGTGTGGACGGATGCAGCAGGAGGAAGGTGGTGTGGACGGATGCAGGAGGA AGCAGCAGGGACGTGGTGTGGACGGATGCAG_____________________________GAGGA CCTGCATCCGTCCACACCACCTTCCTCCTG C AC105450.1 Ensembl:ENSG00000231482 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1480723..1480827 26863196 MeRIP-seq:(Medium) rs1158995226 Functional Loss DEL dbSNP153 32..60 33 - - - 77595 RMVar_ID_77595 Human_SNP_ID_58167845 m1A Human chr2 - 1526932 1526932 1526932 CACAGAGTGTGGGGGATTTGTGGAGGTTGCACAGAGTGGAGGGGATTTGGGGAGGTTGCACACAC CACAGAGTGTGGGGGATTTGTGGAGGTTGCACGGAGTGGAGGGGATTTGGGGAGGTTGCACACAC T C AC105450.1 Ensembl:ENSG00000231482 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1526921..1526992 26863196 MeRIP-seq:(Medium) rs1278413765 Functional Loss SNV dbSNP153 33..33 33 - - - 77596 RMVar_ID_77596 Human_SNP_ID_58168447 m1A Human chr2 + 1527773 1527773 1527773 CCCACTCTGGGCAACCTCCCCAAATCCCCCCCACTCTGTGCAACCTCCCAAAATCCCACACACTG CCCACTCTGGGCAACCTCCCCAAATCCCCCCCCCTCTGTGCAACCTCCCAAAATCCCACACACTG A C TPO Ensembl:ENSG00000115705 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1527770..1528055 26863196 MeRIP-seq:(Medium) rs1314375773 Functional Loss SNV dbSNP153 33..33 33 - - - 77597 RMVar_ID_77597 Human_SNP_ID_58168874 m1A Human chr2 - 1528389 1528387 1528389 TGCACACCGGGTGATTTGAGGAGGTTGCACACAGTGGCGGGATTTGGGGTGGTTGCTCACAATGG TGCACACCGGGTGATTTGAGGAGGTTGCACAC__TGGCGGGATTTGGGGTGGTTGCTCACAATGG ACT A AC105450.1 Ensembl:ENSG00000231482 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1528385..1528482 26863196 MeRIP-seq:(Medium) rs1432717053 Functional Loss DEL dbSNP153 33..34 33 - - - 77598 RMVar_ID_77598 Human_SNP_ID_58168876 m1A Human chr2 - 1528389 1528389 1528389 TGCACACCGGGTGATTTGAGGAGGTTGCACACAGTGGCGGGATTTGGGGTGGTTGCTCACAATGG TGCACACCGGGTGATTTGAGGAGGTTGCACACGGTGGCGGGATTTGGGGTGGTTGCTCACAATGG T C AC105450.1 Ensembl:ENSG00000231482 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1528385..1528482 26863196 MeRIP-seq:(Medium) rs1387595148 Functional Loss SNV dbSNP153 33..33 33 - - - 77599 RMVar_ID_77599 Human_SNP_ID_58173231 m1A Human chr2 + 1534699 1534697 1534699 CCCCCACTCTGTGCAACTTCCAAAAATCCCCCACACAGTGTGCAACCTCCTCAATTCCCTCTAGT CCCCCACTCTGTGCAACTTCCAAAAATCCCC__CACAGTGTGCAACCTCCTCAATTCCCTCTAGT CCA C TPO Ensembl:ENSG00000115705 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1534688..1534764 26863196 MeRIP-seq:(Medium) rs1415030458 Functional Loss DEL dbSNP153 32..33 33 - - - 77600 RMVar_ID_77600 Human_SNP_ID_58173232 m1A Human chr2 + 1534699 1534699 1534699 CCCCCACTCTGTGCAACTTCCAAAAATCCCCCACACAGTGTGCAACCTCCTCAATTCCCTCTAGT CCCCCACTCTGTGCAACTTCCAAAAATCCCCCCCACAGTGTGCAACCTCCTCAATTCCCTCTAGT A C TPO Ensembl:ENSG00000115705 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1534688..1534764 26863196 MeRIP-seq:(Medium) rs1344634330 Functional Loss SNV dbSNP153 33..33 33 - - - 77601 RMVar_ID_77601 Human_SNP_ID_58190723 m1A Human chr2 - 1587609 1587601 1587609 GGCAGGAGGAGAGAGGGACAGTGTTCGGACAGAGGGACAGGGTAGGGACAGAGGGACAGGGCGGG GGCAGGAGGAGAGAGGGACAGTGTTCGGACAG________GGTAGGGACAGAGGGACAGGGCGGG CCTGTCCCT C AC141930.1 Ensembl:ENSG00000228613 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1587570..1587721 26863196 MeRIP-seq:(Medium) rs1342549494 Functional Loss DEL dbSNP153 33..40 33 - - - 77602 RMVar_ID_77602 Human_SNP_ID_58190751 m1A Human chr2 - 1587674 1587666 1587675 TGGGGACAGGGACAGGGTGCGGACAGAGGGACAGCAGGGAGAGAGGGACAGGGACAGAGGGACAG TGGGGACAGGGACAGGGTGCGGACAGAGGGA_________GAGAGGGACAGGGACAGAGGGACAG CTCCCTGCTG C AC141930.1 Ensembl:ENSG00000228613 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1587532..1587913 26863196 MeRIP-seq:(Medium) rs1397754285 Functional Loss DEL dbSNP153 32..40 33 - - - 77603 RMVar_ID_77603 Human_SNP_ID_58190845 m1A Human chr2 - 1587878 1587878 1587878 ACAGGGACAGGGTGAGGACAGAGGGACAGAGCAGGGACAGAGGGACAGAGCGGGGAGAGAGGGAC ACAGGGACAGGGTGAGGACAGAGGGACAGAGCGGGGACAGAGGGACAGAGCGGGGAGAGAGGGAC T C AC141930.1 Ensembl:ENSG00000228613 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1587785..1588139 26863196 MeRIP-seq:(Medium) rs1399913079 Functional Loss SNV dbSNP153 33..33 33 - - - 77604 RMVar_ID_77604 Human_SNP_ID_58191091 m1A Human chr2 - 1588508 1588508 1588508 CTTCAAGGCCCTGCCCAGCTCTCACGTCCAGGAGCCAAGTGGAGCCCAGGGTGGCTTCCGGCCGG CTTCAAGGCCCTGCCCAGCTCTCACGTCCAGGGGCCAAGTGGAGCCCAGGGTGGCTTCCGGCCGG T C AC141930.1 Ensembl:ENSG00000228613 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:1588457..1588580 26863196 MeRIP-seq:(Medium) rs1164996715 Functional Loss SNV dbSNP153 33..33 33 - - - 77605 RMVar_ID_77605 Human_SNP_ID_58207014 m1A Human chr2 - 1638958 1638958 1638958 CCCTCACCACAGTGTTGGGAGACAGGGGGAACATCTCAGCAACAGCACCTCAGCCTTCAGCACAC CCCTCACCACAGTGTTGGGAGACAGGGGGAACGTCTCAGCAACAGCACCTCAGCCTTCAGCACAC T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1638803..1639013 26863196 MeRIP-seq:(Medium) rs776420613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17697559 Human_Splice_Rec_210986,Human_Splice_Rec_211016 RMVar_hsa_circ_5184,RMVar_hsa_circ_83096,RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_123349,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196624,RMVar_hsa_circ_196623,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_13715,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_196626 77606 RMVar_ID_77606 Human_SNP_ID_58208224 m1A Human chr2 - 1643476 1643476 1643476 CCAGGATCCTATGCGACAACGCGGACAACATCACCCGGGTGCAGAGCGACGTGTTCAGGGTGGCG CCAGGATCCTATGCGACAACGCGGACAACATCGCCCGGGTGCAGAGCGACGTGTTCAGGGTGGCG T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1643323..1643606 26863196 MeRIP-seq:(Medium) rs749813167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27475613 Human_miRNA_ID_2394327 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_123349,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196623,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165 77607 RMVar_ID_77607 Human_SNP_ID_58208225 m1A Human chr2 - 1643476 1643476 1643476 CCAGGATCCTATGCGACAACGCGGACAACATCACCCGGGTGCAGAGCGACGTGTTCAGGGTGGCG CCAGGATCCTATGCGACAACGCGGACAACATCCCCCGGGTGCAGAGCGACGTGTTCAGGGTGGCG T G PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1643323..1643606 26863196 MeRIP-seq:(Medium) rs749813167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27475613 Human_miRNA_ID_2394327 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_123349,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196623,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165 77608 RMVar_ID_77608 Human_SNP_ID_58209629 m1A Human chr2 - 1648502 1648502 1648502 CCGGCTGGACGAGAACTTCCAGCCCATTGCACAAGATCACCTCCCCCTTCACAAAGCTTTCTTCT CCGGCTGGACGAGAACTTCCAGCCCATTGCACTAGATCACCTCCCCCTTCACAAAGCTTTCTTCT T A PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:1648451..1648650 26863196 MeRIP-seq:(Medium) rs893014796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_516843,Human_miRNA_ID_521072,Human_miRNA_ID_2383684,Human_miRNA_ID_2471956 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165,RMVar_hsa_circ_319756 77609 RMVar_ID_77609 Human_SNP_ID_58209630 m1A Human chr2 - 1648502 1648502 1648502 CCGGCTGGACGAGAACTTCCAGCCCATTGCACAAGATCACCTCCCCCTTCACAAAGCTTTCTTCT CCGGCTGGACGAGAACTTCCAGCCCATTGCACGAGATCACCTCCCCCTTCACAAAGCTTTCTTCT T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:1648451..1648650 26863196 MeRIP-seq:(Medium) rs893014796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_516843,Human_miRNA_ID_521072,Human_miRNA_ID_2383684,Human_miRNA_ID_2471956 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165,RMVar_hsa_circ_319756 77610 RMVar_ID_77610 Human_SNP_ID_58209920 m1A Human chr2 - 1649100 1649100 1649100 CTGTGTGCGGCAGCGGCATGACTTCGCTGCTCATGAACTCCGTGTACCCGCGGGAGCAGATCAAC CTGTGTGCGGCAGCGGCATGACTTCGCTGCTCGTGAACTCCGTGTACCCGCGGGAGCAGATCAAC T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:1649051..1649288 26863196 MeRIP-seq:(Medium) rs756028395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27475628 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165,RMVar_hsa_circ_319756 77611 RMVar_ID_77611 Human_SNP_ID_58210080 m1A Human chr2 - 1649425 1649425 1649425 TTCAACACCCCTCGGGGCATCAACCCCCACCGACTGTACAACGGGCACGCCCTTCCCATGCCGCG TTCAACACCCCTCGGGGCATCAACCCCCACCGCCTGTACAACGGGCACGCCCTTCCCATGCCGCG T G PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:1649376..1649425 26863196 MeRIP-seq:(Medium) rs906750200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27475638 Human_miRNA_ID_2477168 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165,RMVar_hsa_circ_319756 77612 RMVar_ID_77612 Human_SNP_ID_58210133 m1A Human chr2 - 1649549 1649549 1649549 GGACATGTGCTTCCACCAGAAGTACCGGACGCACGACGGCACCTGTAACAACCTGCAGCACCCCA GGACATGTGCTTCCACCAGAAGTACCGGACGCGCGACGGCACCTGTAACAACCTGCAGCACCCCA T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:1649501..1649600 26863196 MeRIP-seq:(Medium) rs1190799240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8504020,Human_RBP_ID_27475643 Human_miRNA_ID_2889325 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_100100,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196622,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626,RMVar_hsa_circ_330165,RMVar_hsa_circ_319756 77613 RMVar_ID_77613 Human_SNP_ID_58210274 m1A Human chr2 - 1649919 1649917 1649919 AACCATGAGACTGCTAAGTGGGGAGGGGAGACAGGGCCCAGAAACTGGGGCTGTGGAGAGAATAC AACCATGAGACTGCTAAGTGGGGAGGGGAGAC__GGCCCAGAAACTGGGGCTGTGGAGAGAATAC CCT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1649917..1650033 26863196 MeRIP-seq:(Medium) rs1390625231 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626 77614 RMVar_ID_77614 Human_SNP_ID_58210275 m1A Human chr2 - 1649919 1649919 1649919 AACCATGAGACTGCTAAGTGGGGAGGGGAGACAGGGCCCAGAAACTGGGGCTGTGGAGAGAATAC AACCATGAGACTGCTAAGTGGGGAGGGGAGACTGGGCCCAGAAACTGGGGCTGTGGAGAGAATAC T A PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1649917..1650033 26863196 MeRIP-seq:(Medium) rs1183210377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626 77615 RMVar_ID_77615 Human_SNP_ID_58210436 m1A Human chr2 - 1650564 1650564 1650564 CTTTGGCGAACACAGAGATCTGAGTGTGTCTGACCCCAGGACGTGGAGTAGCTGTTGCTTGGAGC CTTTGGCGAACACAGAGATCTGAGTGTGTCTGGCCCCAGGACGTGGAGTAGCTGTTGCTTGGAGC T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1650558..1650675 26863196 MeRIP-seq:(Medium) rs1253858369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23834260 RMVar_hsa_circ_99733,RMVar_hsa_circ_107139,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_91114,RMVar_hsa_circ_196616,RMVar_hsa_circ_196620,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_16269,RMVar_hsa_circ_196626 77616 RMVar_ID_77616 Human_SNP_ID_58211360 m1A Human chr2 + 1654450 1654449 1654450 CGGGTTGAGTTTATAGCTCTGTCAACAGTCGCAATCGCTTCCACGATGGAGGTAGCTACAAACGG CGGGTTGAGTTTATAGCTCTGTCAACAGTCGC_ATCGCTTCCACGATGGAGGTAGCTACAAACGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1654387..1654505 26863196 MeRIP-seq:(Medium) rs1326293208 Functional Loss DEL dbSNP153 33..33 33 - - - 77617 RMVar_ID_77617 Human_SNP_ID_58211597 m1A Human chr2 + 1655322 1655318 1655322 ACGCCACACATAACACATCACACACACGCCACACACAGATACATACCACACACACACCACACATA ACGCCACACATAACACATCACACACACGC____CACAGATACATACCACACACACACCACACATA CCACA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1655316..1655506 26863196 MeRIP-seq:(Medium) rs1028768206 Functional Loss DEL dbSNP153 30..33 33 - - - 77618 RMVar_ID_77618 Human_SNP_ID_58211598 m1A Human chr2 + 1655322 1655318 1655322 ACGCCACACATAACACATCACACACACGCCACACACAGATACATACCACACACACACCACACATA ACGCCACACATAACACATCACACACACGCCA__CACAGATACATACCACACACACACCACACATA CCACA CCA - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1655316..1655506 26863196 MeRIP-seq:(Medium) rs1028768206 Functional Loss DEL dbSNP153 32..33 33 - - - 77619 RMVar_ID_77619 Human_SNP_ID_58211865 m1A Human chr2 + 1656068 1656068 1656068 ACCAACACCATAGCATACCACACATACTCATCACACTATAAACACACAGACACACCACACAACAC ACCAACACCATAGCATACCACACATACTCATCCCACTATAAACACACAGACACACCACACAACAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:1656065..1656168 26863196 MeRIP-seq:(Medium) rs1446459640 Functional Loss SNV dbSNP153 33..33 33 - - - 77620 RMVar_ID_77620 Human_SNP_ID_58212103 m1A Human chr2 - 1656869 1656869 1656869 GGGTAGGTCCCTGTCCGGAGAGGGCAGGTTTCAGTCAGGAGGGGGCAAGTCCCTGTCAAGAGGGT GGGTAGGTCCCTGTCCGGAGAGGGCAGGTTTCGGTCAGGAGGGGGCAAGTCCCTGTCAAGAGGGT T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1656867..1657045 26863196 MeRIP-seq:(Medium) rs1330266166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77621 RMVar_ID_77621 Human_SNP_ID_58212134 m1A Human chr2 - 1656920 1656920 1656920 GGCAGGAGGGGACAGGTTTCTGTCAGGAGGGGACAGGTTCCAGTCAGGAGGGGGTAGGTCCCTGT GGCAGGAGGGGACAGGTTTCTGTCAGGAGGGGGCAGGTTCCAGTCAGGAGGGGGTAGGTCCCTGT T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1656918..1657004 26863196 MeRIP-seq:(Medium) rs1158525373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77622 RMVar_ID_77622 Human_SNP_ID_58212210 m1A Human chr2 - 1657163 1657138 1657164 AGGAGGAGGTGGCAGGTTCCCCCCCAGTCAGTAGGAGGCAGGTCCCCCCCCAGTCAGGAGGGGTA AGGAGGAGGTGGCAGGTTCCCCCCCAGTCAG__________________________GAGGGGTA CCTGACTGGGGGGGGACCTGCCTCCTA C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1657160..1657293 26863196 MeRIP-seq:(Medium) rs1310993192 Functional Loss DEL dbSNP153 32..57 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77623 RMVar_ID_77623 Human_SNP_ID_58212289 m1A Human chr2 + 1657343 1657343 1657343 CCTCCTGACAGAAACCAGCCCCAACCTGACTGAAACCAGCCCCAACCTGACTGAAACCTGCCAAC CCTCCTGACAGAAACCAGCCCCAACCTGACTGCAACCAGCCCCAACCTGACTGAAACCTGCCAAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1657341..1657704 26863196 MeRIP-seq:(Medium) rs1275924613 Functional Loss SNV dbSNP153 33..33 33 - - - 77624 RMVar_ID_77624 Human_SNP_ID_58212306 m1A Human chr2 + 1657387 1657387 1657387 ACCTGACTGAAACCTGCCAACTCCTGACTGAGACCTGTCTTCTCCTGAAGGGGACCTGCCCTGTC ACCTGACTGAAACCTGCCAACTCCTGACTGAGTCCTGTCTTCTCCTGAAGGGGACCTGCCCTGTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1657384..1657723 26863196 MeRIP-seq:(Medium) rs984419348 Functional Loss SNV dbSNP153 33..33 33 - - - 77625 RMVar_ID_77625 Human_SNP_ID_58212504 m1A Human chr2 - 1657955 1657924 1657956 AGAAAGGAAATCACAGTGAGGGGGCAAGTCCCAGTGAGGAGGGGGCAAGAGGGGGCAGGTTCCTG AGAAAGGAAATCACAGTGAGGGGGCAAGTCC________________________________TG AGGAACCTGCCCCCTCTTGCCCCCTCCTCACTG A PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1657944..1658439 26863196 MeRIP-seq:(Medium) rs1040764063 Functional Loss DEL dbSNP153 32..63 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77626 RMVar_ID_77626 Human_SNP_ID_58212515 m1A Human chr2 + 1657959 1657938 1657959 AACCTGCCCCCTCTTGCCCCCTCCTCACTGGGACTTGCCCCCTCACTGTGATTTCCTTTCTCCTT AACCTGCCCCCT_____________________CTTGCCCCCTCACTGTGATTTCCTTTCTCCTT TCTTGCCCCCTCCTCACTGGGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1657956..1658030 26863196 MeRIP-seq:(Medium) rs1235955342 Functional Loss DEL dbSNP153 13..33 33 - - - 77627 RMVar_ID_77627 Human_SNP_ID_58212525 m1A Human chr2 + 1657953 1657953 1657953 GACAGGAACCTGCCCCCTCTTGCCCCCTCCTCACTGGGACTTGCCCCCTCACTGTGATTTCCTTT GACAGGAACCTGCCCCCTCTTGCCCCCTCCTCTCTGGGACTTGCCCCCTCACTGTGATTTCCTTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1657943..1658015 26863196 MeRIP-seq:(Medium) rs1389956254 Functional Loss SNV dbSNP153 33..33 33 - - - 77628 RMVar_ID_77628 Human_SNP_ID_58212548 m1A Human chr2 - 1658004 1658004 1658004 GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCAGGAGGAAGAGACAAGGAGAAAGGAAATCACAG GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCTGGAGGAAGAGACAAGGAGAAAGGAAATCACAG T A PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:1657971..1658085 26863196 MeRIP-seq:(Medium) rs536446224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77629 RMVar_ID_77629 Human_SNP_ID_58212549 m1A Human chr2 - 1658004 1658004 1658004 GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCAGGAGGAAGAGACAAGGAGAAAGGAAATCACAG GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCCGGAGGAAGAGACAAGGAGAAAGGAAATCACAG T G PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:1657971..1658085 26863196 MeRIP-seq:(Medium) rs536446224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77630 RMVar_ID_77630 Human_SNP_ID_58212678 m1A Human chr2 - 1658096 1658060 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGT_________________________________ CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGTT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1188132450 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77631 RMVar_ID_77631 Human_SNP_ID_58212716 m1A Human chr2 - 1658096 1658070 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGT__________________________GAGAGAG CTCTCTCTCTCTCTCTCTCTCTCTGTT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1558494454 Functional Loss DEL dbSNP153 33..58 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77632 RMVar_ID_77632 Human_SNP_ID_58212721 m1A Human chr2 - 1658096 1658072 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGT________________________GAGAGAGAG CTCTCTCTCTCTCTCTCTCTCTGTT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1392521679 Functional Loss DEL dbSNP153 33..56 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77633 RMVar_ID_77633 Human_SNP_ID_58212737 m1A Human chr2 - 1658096 1658080 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGT________________GAGAGAGAGAGAGAGAG CTCTCTCTCTCTCTGTT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs750482583 Functional Loss DEL dbSNP153 33..48 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77634 RMVar_ID_77634 Human_SNP_ID_58212768 m1A Human chr2 - 1658096 1658092 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGT____GAGAGAGAGAGAGAGAGAGAGAGAGAGAG CTGTT C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1190448834 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77635 RMVar_ID_77635 Human_SNP_ID_58212770 m1A Human chr2 - 1658096 1658093 1658097 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTG____AGAGAGAGAGAGAGAGAGAGAGAGAGAGAG TGTTA T PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1399798472 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77636 RMVar_ID_77636 Human_SNP_ID_58212773 m1A Human chr2 - 1658096 1658096 1658096 AGACACTGAGAGTGGACGCACGCAGACACTGTAACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG AGACACTGAGAGTGGACGCACGCAGACACTGTGACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658085..1658171 26863196 MeRIP-seq:(Medium) rs1163044081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 77637 RMVar_ID_77637 Human_SNP_ID_58212848 m1A Human chr2 + 1658248 1658248 1658248 CTGTGTGGTTCCACTTCACGCTGTTGTCTTCAAATTTACACCATCGTCCTGACCTCTCCCTGCAG CTGTGTGGTTCCACTTCACGCTGTTGTCTTCATATTTACACCATCGTCCTGACCTCTCCCTGCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658245..1658497 26863196 MeRIP-seq:(Medium) rs1249949757 Functional Loss SNV dbSNP153 33..33 33 - - - 77638 RMVar_ID_77638 Human_SNP_ID_58213091 m1A Human chr2 + 1658827 1658827 1658827 ACTCTACTCTCCCAGACCAGGCTGCCCCTGCCACCCCCCATCTCCCCGCGGCTCCCTCTGCTCAG ACTCTACTCTCCCAGACCAGGCTGCCCCTGCCCCCCCCCATCTCCCCGCGGCTCCCTCTGCTCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1658817..1658937 26863196 MeRIP-seq:(Medium) rs547755016 Functional Loss SNV dbSNP153 33..33 33 - - - 77639 RMVar_ID_77639 Human_SNP_ID_58219079 m1A Human chr2 - 1680300 1680300 1680300 CTGTGAAATCCTGTGGTTGGCGGATTTGCTGAAAACCTACGCGGAGTCGGGGAACGCGCAGGCAG CTGTGAAATCCTGTGGTTGGCGGATTTGCTGACAACCTACGCGGAGTCGGGGAACGCGCAGGCAG T G PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:1680276..1680300 26863196 MeRIP-seq:(Medium) rs1193579432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_210958,Human_Splice_Rec_211048,Human_Splice_Rec_211092,Human_Splice_Rec_211104,Human_Splice_Rec_211118 RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_19997,RMVar_hsa_circ_14491,RMVar_hsa_circ_111431,RMVar_hsa_circ_196627,RMVar_hsa_circ_338685,RMVar_hsa_circ_370308,RMVar_hsa_circ_107135,RMVar_hsa_circ_196632,RMVar_hsa_circ_196633,RMVar_hsa_circ_196631,RMVar_hsa_circ_346432,RMVar_hsa_circ_349549,RMVar_hsa_circ_325190,RMVar_hsa_circ_36333,RMVar_hsa_circ_196634,RMVar_hsa_circ_74522,RMVar_hsa_circ_40790,RMVar_hsa_circ_376823,RMVar_hsa_circ_372096,RMVar_hsa_circ_196636 77640 RMVar_ID_77640 Human_SNP_ID_58222517 m1A Human chr2 - 1693120 1693120 1693120 TTTCTTGTTTCTTCACAGAGATCTTCGCTTTAACAGAATCAGAGAGATCCAACCTGGGGCATTCA TTTCTTGTTTCTTCACAGAGATCTTCGCTTTAGCAGAATCAGAGAGATCCAACCTGGGGCATTCA T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:1693101..1693150 26863196 MeRIP-seq:(Medium) rs553369438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_210948,Human_Splice_Rec_210949,Human_Splice_Rec_211038,Human_Splice_Rec_211039,Human_Splice_Rec_211096,Human_Splice_Rec_211097,Human_Splice_Rec_211108,Human_Splice_Rec_211109 RMVar_hsa_circ_325190,RMVar_hsa_circ_35871,RMVar_hsa_circ_196634,RMVar_hsa_circ_74522,RMVar_hsa_circ_372096,RMVar_hsa_circ_196636,RMVar_hsa_circ_289083 77641 RMVar_ID_77641 Human_SNP_ID_58227574 m1A Human chr2 - 1710494 1710478 1710495 TGGGTCCTGGTGGAGAGTGGGTGCTAGTGGAGAGTGGGTGCTGGTGGAAAGTGGATGCTGGTGGA TGGGTCCTGGTGGAGAGTGGGTGCTAGTGGA_________________AAGTGGATGCTGGTGGA TTCCACCAGCACCCACTC T PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1710492..1710762 26863196 MeRIP-seq:(Medium) rs1227390323 Functional Loss DEL dbSNP153 32..48 33 - - - 77642 RMVar_ID_77642 Human_SNP_ID_58227580 m1A Human chr2 - 1710494 1710492 1710494 TGGGTCCTGGTGGAGAGTGGGTGCTAGTGGAGAGTGGGTGCTGGTGGAAAGTGGATGCTGGTGGA TGGGTCCTGGTGGAGAGTGGGTGCTAGTGGAG__TGGGTGCTGGTGGAAAGTGGATGCTGGTGGA ACT A PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1710492..1710762 26863196 MeRIP-seq:(Medium) rs1178515850 Functional Loss DEL dbSNP153 33..34 33 - - - 77643 RMVar_ID_77643 Human_SNP_ID_58227699 m1A Human chr2 + 1710652 1710652 1710652 ACTCTCCACCAGCACCCACTCTATGAACACCCACTCTCCACCAGCACCCGCTCTACCAGCACCCA ACTCTCCACCAGCACCCACTCTATGAACACCCCCTCTCCACCAGCACCCGCTCTACCAGCACCCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:1710456..1711073 26863196 MeRIP-seq:(Medium) rs1296338787 Functional Loss SNV dbSNP153 33..33 33 - - - 77644 RMVar_ID_77644 Human_SNP_ID_58227850 m1A Human chr2 + 1710870 1710870 1710870 CCACTCCACCAGCACCCACTCCACCAGCACCCACTCTCCACCAGCACCTGCTCCACCAGCACCCA CCACTCCACCAGCACCCACTCCACCAGCACCCCCTCTCCACCAGCACCTGCTCCACCAGCACCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1710867..1711017 26863196 MeRIP-seq:(Medium) rs954964249 Functional Loss SNV dbSNP153 33..33 33 - - - 77645 RMVar_ID_77645 Human_SNP_ID_58227851 m1A Human chr2 + 1710870 1710870 1710870 CCACTCCACCAGCACCCACTCCACCAGCACCCACTCTCCACCAGCACCTGCTCCACCAGCACCCA CCACTCCACCAGCACCCACTCCACCAGCACCCGCTCTCCACCAGCACCTGCTCCACCAGCACCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1710867..1711017 26863196 MeRIP-seq:(Medium) rs954964249 Functional Loss SNV dbSNP153 33..33 33 - - - 77646 RMVar_ID_77646 Human_SNP_ID_58227993 m1A Human chr2 + 1711139 1711139 1711139 ACTCCACCAGCACCCACTCTCCACCAGCACCCACTCTCCACCAGCACCCGCTCCACCAGCACCCA ACTCCACCAGCACCCACTCTCCACCAGCACCCCCTCTCCACCAGCACCCGCTCCACCAGCACCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1711131..1711396 26863196 MeRIP-seq:(Medium) rs111161802 Functional Loss SNV dbSNP153 33..33 33 - - - 77647 RMVar_ID_77647 Human_SNP_ID_58227994 m1A Human chr2 + 1711139 1711139 1711139 ACTCCACCAGCACCCACTCTCCACCAGCACCCACTCTCCACCAGCACCCGCTCCACCAGCACCCA ACTCCACCAGCACCCACTCTCCACCAGCACCCGCTCTCCACCAGCACCCGCTCCACCAGCACCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1711131..1711396 26863196 MeRIP-seq:(Medium) rs111161802 Functional Loss SNV dbSNP153 33..33 33 - - - 77648 RMVar_ID_77648 Human_SNP_ID_58229857 m1A Human chr2 - 1717651 1717651 1717651 CTGCAGGTCAGTAGAGTAGTCCATGTGGTTCCAGGCTCAGGATCAGCTATTTTGTGATTCTGTCT CTGCAGGTCAGTAGAGTAGTCCATGTGGTTCCGGGCTCAGGATCAGCTATTTTGTGATTCTGTCT T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1717648..1718639 26863196 MeRIP-seq:(Medium) rs915200156 Functional Loss SNV dbSNP153 33..33 33 - - - 77649 RMVar_ID_77649 Human_SNP_ID_58229908 m1A Human chr2 - 1717838 1717838 1717838 AGAATAGCCTTGGGTGGTCGGTTAGTGGGTAGAGCAGGTTTGGGTAGTTGGTTAGCAGAATAGCT AGAATAGCCTTGGGTGGTCGGTTAGTGGGTAGGGCAGGTTTGGGTAGTTGGTTAGCAGAATAGCT T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:1717771..1717884 26863196 MeRIP-seq:(Medium) rs1030770743 Functional Loss SNV dbSNP153 33..33 33 - - - 77650 RMVar_ID_77650 Human_SNP_ID_58229916 m1A Human chr2 - 1717867 1717867 1717867 GGTAGGGCAGGTTTGGGTAGGTGGTTAGTAGAATAGCCTTGGGTGGTCGGTTAGTGGGTAGAGCA GGTAGGGCAGGTTTGGGTAGGTGGTTAGTAGAGTAGCCTTGGGTGGTCGGTTAGTGGGTAGAGCA T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:1717702..1717992 26863196 MeRIP-seq:(Medium) rs1400081554 Functional Loss SNV dbSNP153 33..33 33 - - - 77651 RMVar_ID_77651 Human_SNP_ID_58230060 m1A Human chr2 + 1718409 1718409 1718409 TACCACCCAAACCTACTCTATTAACGTATGTCACTAACCTACCACCTAAACTTACTCTACTAACC TACCACCCAAACCTACTCTATTAACGTATGTCGCTAACCTACCACCTAAACTTACTCTACTAACC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:1718167..1718607 26863196 MeRIP-seq:(Medium) rs1328928605 Functional Loss SNV dbSNP153 33..33 33 - - - 77652 RMVar_ID_77652 Human_SNP_ID_58239163 m1A Human chr2 - 1750673 1750673 1750673 GGGAGGGAGGGAGGGAGGGGGGGAGGGGGGGGAGGGAGGGAGGGGGGGGAGGGAGGGAGGGAGGG GGGAGGGAGGGAGGGAGGGGGGGAGGGGGGGGGGGGAGGGAGGGGGGGGAGGGAGGGAGGGAGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:1750638..1750768 26863196 MeRIP-seq:(Medium) rs1364129430 Functional Loss SNV dbSNP153 33..33 33 - - - 77653 RMVar_ID_77653 Human_SNP_ID_58620906 m1A Human chr2 - 3183425 3183425 3183425 TGAGGACCTCAGGGCTAGAGAAAGTGGGTGCCAGGCAGGGGACAGTCAGGCTGGGTTGGATAGGT TGAGGACCTCAGGGCTAGAGAAAGTGGGTGCCCGGCAGGGGACAGTCAGGCTGGGTTGGATAGGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3183406..3183528 26863196 MeRIP-seq:(Medium) rs945928457 Functional Loss SNV dbSNP153 33..33 33 - - - 77654 RMVar_ID_77654 Human_SNP_ID_58621641 m1A Human chr2 - 3186036 3186036 3186036 ACAGCAGGAGCAGCATGAACTGCAGGAGCGGCACGGGATAAGAGAGGTAGGAAGCTGGGAGCGGG ACAGCAGGAGCAGCATGAACTGCAGGAGCGGCGCGGGATAAGAGAGGTAGGAAGCTGGGAGCGGG T C lnc-EIPR1-6 RNACentral:URS00008C3BFE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3186020..3186103 26863196 MeRIP-seq:(Medium) rs1193404619 Functional Loss SNV dbSNP153 33..33 33 - - - 77655 RMVar_ID_77655 Human_SNP_ID_58621888 m1A Human chr2 + 3186983 3186983 3186983 CTGGGCCTCCTGCCTCATTCCCATGCCAGCCCAGCTGCCTCCCTACCTGATCCACTCACCCAGGT CTGGGCCTCCTGCCTCATTCCCATGCCAGCCCGGCTGCCTCCCTACCTGATCCACTCACCCAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3186934..3187079 26863196 MeRIP-seq:(Medium) rs4497900 Functional Loss SNV dbSNP153 33..33 33 - - - 77656 RMVar_ID_77656 Human_SNP_ID_58621889 m1A Human chr2 + 3186983 3186983 3186985 CTGGGCCTCCTGCCTCATTCCCATGCCAGCCCAGCTGCCTCCCTACCTGATCCACTCACCCAGGT CTGGGCCTCCTGCCTCATTCCCATGCCAGCCCGGGTGCCTCCCTACCTGATCCACTCACCCAGGT AGC GGG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3186934..3187079 26863196 MeRIP-seq:(Medium) rs386642479 Functional Loss MNV dbSNP153 33..35 33 - - - 77657 RMVar_ID_77657 Human_SNP_ID_58647285 m1A Human chr2 - 3277175 3277175 3277175 GTGGAGACAGGTGTGGGGCCGCGTGGGTGGAGAGGCTCCTGGATTTCTGTGGTTTCTCCCCCAAC GTGGAGACAGGTGTGGGGCCGCGTGGGTGGAGTGGCTCCTGGATTTCTGTGGTTTCTCCCCCAAC T A EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3277171..3277308 26863196 MeRIP-seq:(Medium) rs1262633685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200214,Human_RBP_ID_9428519,Human_RBP_ID_18947511 RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_337810,RMVar_hsa_circ_319957,RMVar_hsa_circ_196690 77658 RMVar_ID_77658 Human_SNP_ID_58647295 m1A Human chr2 + 3277194 3277194 3277194 AAATCCAGGAGCCTCTCCACCCACGCGGCCCCACACCTGTCTCCACCCACACGGCCCCGCACCTG AAATCCAGGAGCCTCTCCACCCACGCGGCCCCGCACCTGTCTCCACCCACACGGCCCCGCACCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3277190..3277305 26863196 MeRIP-seq:(Medium) rs1004892094 Functional Loss SNV dbSNP153 33..33 33 - - - 77659 RMVar_ID_77659 Human_SNP_ID_58652290 m1A Human chr2 - 3294549 3294483 3294549 CAGAGGATCGGCTGGATGGAGGGTGTGTGTAGAGAGGATCGGCTGGATGGAGGGTGTGTGCAGAG CAGAGGATCGGCTGGATGGAGGGTGTGTGTAG_________________________________ CCTACACACACACACCCTCCATCCAGCCGATCCTCTCTGCACACACCCTCCATCCAGCCGATCCTCT C EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:3294232..3296874;chr2:3294193..3296884;chr2:3294203..3296844 26863196 MeRIP-seq:(Medium) rs1558279281 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5470760,Human_RBP_ID_8200237,Human_RBP_ID_23119245,Human_RBP_ID_23868856 RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_337810,RMVar_hsa_circ_319957,RMVar_hsa_circ_196690 77660 RMVar_ID_77660 Human_SNP_ID_58652942 m1A Human chr2 + 3295769 3295766 3295770 CACACCCTCCATCCAGCCCGTCCTCTCTCTGCACACACACCCTCCATCCAGCCCATCCTCTCTAC CACACCCTCCATCCAGCCCGTCCTCTCTCT____ACACACCCTCCATCCAGCCCATCCTCTCTAC TGCAC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:3295622..3296084 26863196 MeRIP-seq:(Medium) rs1168935486 Functional Loss DEL dbSNP153 31..34 33 - - - 77661 RMVar_ID_77661 Human_SNP_ID_58652944 m1A Human chr2 + 3295769 3295767 3295769 CACACCCTCCATCCAGCCCGTCCTCTCTCTGCACACACACCCTCCATCCAGCCCATCCTCTCTAC CACACCCTCCATCCAGCCCGTCCTCTCTCTG__CACACACCCTCCATCCAGCCCATCCTCTCTAC GCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:3295622..3296084 26863196 MeRIP-seq:(Medium) rs1354757012 Functional Loss DEL dbSNP153 32..33 33 - - - 77662 RMVar_ID_77662 Human_SNP_ID_58652948 m1A Human chr2 + 3295769 3295769 3295769 CACACCCTCCATCCAGCCCGTCCTCTCTCTGCACACACACCCTCCATCCAGCCCATCCTCTCTAC CACACCCTCCATCCAGCCCGTCCTCTCTCTGCCCACACACCCTCCATCCAGCCCATCCTCTCTAC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:3295622..3296084 26863196 MeRIP-seq:(Medium) rs1403154777 Functional Loss SNV dbSNP153 33..33 33 - - - 77663 RMVar_ID_77663 Human_SNP_ID_58653399 m1A Human chr2 + 3296583 3296583 3296583 CTCTGTATACACACACACACTCCATCCAGCCCATCCTCTCTACACATACACCCTCCATCCAGCCC CTCTGTATACACACACACACTCCATCCAGCCCGTCCTCTCTACACATACACCCTCCATCCAGCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:3296477..3296674 26863196 MeRIP-seq:(Medium) rs529628219 Functional Loss SNV dbSNP153 33..33 33 - - - 77664 RMVar_ID_77664 Human_SNP_ID_58655489 m1A Human chr2 - 3304475 3304475 3304475 GCTGAACTGATGGGACTGGAGGGCTGAACTGGACGGGAGTGGAGGGCTGAATTGGACGGGACTGA GCTGAACTGATGGGACTGGAGGGCTGAACTGGGCGGGAGTGGAGGGCTGAATTGGACGGGACTGA T C EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3304286..3304489 26863196 MeRIP-seq:(Medium) rs1436579321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_337810,RMVar_hsa_circ_319957,RMVar_hsa_circ_196690 77665 RMVar_ID_77665 Human_SNP_ID_58658688 m1A Human chr2 + 3314966 3314966 3314966 CTGGCAAGGCCCTGCCCTGGCGGTGTCCACACAGCATCTTCTGCTGCTGCTCTCCGGCAAACTGC CTGGCAAGGCCCTGCCCTGGCGGTGTCCACACGGCATCTTCTGCTGCTGCTCTCCGGCAAACTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3314965..3315164 26863196 MeRIP-seq:(Medium) rs140045721 Functional Loss SNV dbSNP153 33..33 33 - - - 77666 RMVar_ID_77666 Human_SNP_ID_58662981 m1A Human chr2 + 3329147 3329147 3329147 ATGATCTCAGGGCACCAGCCTGGGCTCCCCTGAATCAGAGCCCACCCACCAGGCTCTAATGATCT ATGATCTCAGGGCACCAGCCTGGGCTCCCCTGGATCAGAGCCCACCCACCAGGCTCTAATGATCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3329094..3329848 26863196 MeRIP-seq:(Medium) rs1300907732 Functional Loss SNV dbSNP153 33..33 33 - - - 77667 RMVar_ID_77667 Human_SNP_ID_58663074 m1A Human chr2 + 3329344 3329344 3329344 CCCCTGAATCAGAGCCCACCCACCACGCTCTAATGATCTCGGGATGCCAGCCTGGGCTTCCTTGG CCCCTGAATCAGAGCCCACCCACCACGCTCTAGTGATCTCGGGATGCCAGCCTGGGCTTCCTTGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:3329188..3329368 26863196 MeRIP-seq:(Medium) rs556227462 Functional Loss SNV dbSNP153 33..33 33 - - - 77668 RMVar_ID_77668 Human_SNP_ID_58663162 m1A Human chr2 - 3329600 3329600 3329600 ATTAGAGCATGGTGGGTAGATCTGTGATCTAGAGGAGTCCAGGCTAGTACCCTGAGATCATTAGA ATTAGAGCATGGTGGGTAGATCTGTGATCTAGGGGAGTCCAGGCTAGTACCCTGAGATCATTAGA T C EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3329598..3329676 26863196 MeRIP-seq:(Medium) rs1346167421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_337810,RMVar_hsa_circ_319957,RMVar_hsa_circ_196690 77669 RMVar_ID_77669 Human_SNP_ID_58670225 m1A Human chr2 - 3354631 3354631 3354631 ATGTGCATGTGTTTTTCTTCCCTCCTGCAGGCACGTGCCTTAACACCTCAAACTGCAGAAACAGA ATGTGCATGTGTTTTTCTTCCCTCCTGCAGGCGCGTGCCTTAACACCTCAAACTGCAGAAACAGA T C EIPR1 Ensembl:ENSG00000032389 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3354614..3354690 26863196 MeRIP-seq:(Medium) rs1056644591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18998904,Human_RBP_ID_25574386 Human_Splice_Rec_212762,Human_Splice_Rec_212763,Human_Splice_Rec_212780,Human_Splice_Rec_212781,Human_Splice_Rec_212800,Human_Splice_Rec_212801,Human_Splice_Rec_212820,Human_Splice_Rec_212821,Human_Splice_Rec_212836,Human_Splice_Rec_212837,Human_Splice_Rec_212848,Human_Splice_Rec_212849,Human_Splice_Rec_212858,Human_Splice_Rec_212859,Human_Splice_Rec_212872,Human_Splice_Rec_212873 RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_299378,RMVar_hsa_circ_196692,RMVar_hsa_circ_196691 77670 RMVar_ID_77670 Human_SNP_ID_58676449 m1A Human chr2 + 3377777 3377777 3377777 CCGGCGCGTCCCCACCTCGCGGGCGTGTTCCCAGCGCCCATTCATTCCCTCCCCGCAGCAAACGA CCGGCGCGTCCCCACCTCGCGGGCGTGTTCCCGGCGCCCATTCATTCCCTCCCCGCAGCAAACGA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:3377658..3377825 26863196 MeRIP-seq:(Medium) rs1489747722 Functional Loss SNV dbSNP153 33..33 33 - - - 77671 RMVar_ID_77671 Human_SNP_ID_58676455 m1A Human chr2 + 3377784 3377784 3377784 GTCCCCACCTCGCGGGCGTGTTCCCAGCGCCCATTCATTCCCTCCCCGCAGCAAACGACTCCAAA GTCCCCACCTCGCGGGCGTGTTCCCAGCGCCCTTTCATTCCCTCCCCGCAGCAAACGACTCCAAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:3377626..3377850;chr2:3377606..3377850;chr2:3377655..3377803 26863196 MeRIP-seq:(Medium) rs1306791753 Functional Loss SNV dbSNP153 33..33 33 - - - 77672 RMVar_ID_77672 Human_SNP_ID_58679363 m1A Human chr2 + 3387664 3387664 3387664 CGCTGGCGGCGGCGAGGAGACCCCGGCCCCGGAGGCCCCGCACCCCCCTCAGCTCGCGCCTCCGG CGCTGGCGGCGGCGAGGAGACCCCGGCCCCGGTGGCCCCGCACCCCCCTCAGCTCGCGCCTCCGG A T TRAPPC12 Ensembl:ENSG00000171853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3387601..3388078 26863196 MeRIP-seq:(Medium) rs760340783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243168,Human_RBP_ID_917466,Human_RBP_ID_5322363,Human_RBP_ID_19001099,Human_RBP_ID_22450111 Human_Splice_Rec_212882,Human_Splice_Rec_212904,Human_Splice_Rec_212926 Human_miRNA_ID_3065385 RMVar_hsa_circ_96002,RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_83933,RMVar_hsa_circ_340106,RMVar_hsa_circ_196694,RMVar_hsa_circ_352761,RMVar_hsa_circ_296714,RMVar_hsa_circ_196697,RMVar_hsa_circ_196698,RMVar_hsa_circ_196696 77673 RMVar_ID_77673 Human_SNP_ID_58679413 m1A Human chr2 - 3387730 3387730 3387730 CTTCGGATCCAAACTCATCTCCGCCAAGATCGATGGTTTCCTCCTGGAAGAGCAACCCCTGCTCC CTTCGGATCCAAACTCATCTCCGCCAAGATCGTTGGTTTCCTCCTGGAAGAGCAACCCCTGCTCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:3379767..3387775 26863196 MeRIP-seq:(Medium) rs1333921927 Functional Loss SNV dbSNP153 33..33 33 - - - 77674 RMVar_ID_77674 Human_SNP_ID_58679663 m1A Human chr2 - 3388146 3388146 3388146 GAAGCTGGGCGACTTCACCATCTGCGGCTCGAAGCCGTCCCCGGAGGCTGGGGGCGCGCGCTGGC GAAGCTGGGCGACTTCACCATCTGCGGCTCGAGGCCGTCCCCGGAGGCTGGGGGCGCGCGCTGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:3388076..3388415 26863196 MeRIP-seq:(Medium) rs1337438213 Functional Loss SNV dbSNP153 33..33 33 - - - 77675 RMVar_ID_77675 Human_SNP_ID_58679683 m1A Human chr2 - 3388197 3388197 3388197 GGGCTGCACGACCTGGGGCGGTGTCCTGGCCGAGGCCTCGCTGGCGCCACCGAAGCTGGGCGACT GGGCTGCACGACCTGGGGCGGTGTCCTGGCCGCGGCCTCGCTGGCGCCACCGAAGCTGGGCGACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3388146..3388598 26863196 MeRIP-seq:(Medium) rs1399690946 Functional Loss SNV dbSNP153 33..33 33 - - - 77676 RMVar_ID_77676 Human_SNP_ID_58679697 m1A Human chr2 + 3388216 3388216 3388216 CGCCAGCGAGGCCTCGGCCAGGACACCGCCCCAGGTCGTGCAGCCCAGCCCCAGCCTCAGCACGT CGCCAGCGAGGCCTCGGCCAGGACACCGCCCCGGGTCGTGCAGCCCAGCCCCAGCCTCAGCACGT A G TRAPPC12 Ensembl:ENSG00000171853 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:3387876..3388667 26863410 MeRIP-seq:(Medium) rs1223387451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9297005,Human_RBP_ID_18759725 Human_miRNA_ID_2386333,Human_miRNA_ID_2387805,Human_miRNA_ID_2398963,Human_miRNA_ID_2552519,Human_miRNA_ID_2683026,Human_miRNA_ID_3030010 RMVar_hsa_circ_96002,RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_83933,RMVar_hsa_circ_340106,RMVar_hsa_circ_196694,RMVar_hsa_circ_352761,RMVar_hsa_circ_296714,RMVar_hsa_circ_196697,RMVar_hsa_circ_196698,RMVar_hsa_circ_196696 77677 RMVar_ID_77677 Human_SNP_ID_58679744 m1A Human chr2 - 3388278 3388278 3388278 GGTAGTAAAGGAGTCGAAGAAGTCCGAGGCCAAGGAGTGGCTGGCGGCCGTGTCTCCGAAGAACG GGTAGTAAAGGAGTCGAAGAAGTCCGAGGCCAGGGAGTGGCTGGCGGCCGTGTCTCCGAAGAACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3388101..3388612 26863196 MeRIP-seq:(Medium) rs781187492 Functional Loss SNV dbSNP153 33..33 33 - - - 77678 RMVar_ID_77678 Human_SNP_ID_58679753 m1A Human chr2 + 3388297 3388297 3388297 CGCCAGCCACTCCTTGGCCTCGGACTTCTTCGACTCCTTTACTACCTCCGCCTTCATTTCCGTCA CGCCAGCCACTCCTTGGCCTCGGACTTCTTCGTCTCCTTTACTACCTCCGCCTTCATTTCCGTCA A T TRAPPC12 Ensembl:ENSG00000171853 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:3388151..3388617 26863196 MeRIP-seq:(Medium) rs375509137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18759726,Human_RBP_ID_27479790 Human_miRNA_ID_1913294,Human_miRNA_ID_1915742,Human_miRNA_ID_1918191,Human_miRNA_ID_1920646,Human_miRNA_ID_1923104,Human_miRNA_ID_1925556,Human_miRNA_ID_1928007,Human_miRNA_ID_1930458,Human_miRNA_ID_2167695,Human_miRNA_ID_2169220,Human_miRNA_ID_2628285,Human_miRNA_ID_2641396,Human_miRNA_ID_3124139 RMVar_hsa_circ_96002,RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_83933,RMVar_hsa_circ_340106,RMVar_hsa_circ_196694,RMVar_hsa_circ_352761,RMVar_hsa_circ_296714,RMVar_hsa_circ_196697,RMVar_hsa_circ_196698,RMVar_hsa_circ_196696 77679 RMVar_ID_77679 Human_SNP_ID_58695989 m1A Human chr2 - 3448619 3448587 3448619 CCACGCCCTACCCTCGCGTAACCGGCTGCTCTAGACGCCCTACCCTCGAGTAACCGGCTGCTCTC CCACGCCCTACCCTCGCGTAACCGGCTGCTCT________________________________C GAGAGCAGCCGGTTACTCGAGGGTAGGGCGTCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:3448509..3448661;chr2:3448537..3448800 26863196 MeRIP-seq:(Medium) rs1289963608 Functional Loss DEL dbSNP153 33..64 33 - - - 77680 RMVar_ID_77680 Human_SNP_ID_58696014 m1A Human chr2 - 3448619 3448618 3448620 CCACGCCCTACCCTCGCGTAACCGGCTGCTCTAGACGCCCTACCCTCGAGTAACCGGCTGCTCTC CCACGCCCTACCCTCGCGTAACCGGCTGCTC__GACGCCCTACCCTCGAGTAACCGGCTGCTCTC CTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:3448509..3448661;chr2:3448537..3448800 26863196 MeRIP-seq:(Medium) rs1558391062 Functional Loss DEL dbSNP153 32..33 33 - - - 77681 RMVar_ID_77681 Human_SNP_ID_58696015 m1A Human chr2 - 3448619 3448619 3448619 CCACGCCCTACCCTCGCGTAACCGGCTGCTCTAGACGCCCTACCCTCGAGTAACCGGCTGCTCTC CCACGCCCTACCCTCGCGTAACCGGCTGCTCTCGACGCCCTACCCTCGAGTAACCGGCTGCTCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:3448509..3448661;chr2:3448537..3448800 26863196 MeRIP-seq:(Medium) rs4971507 Functional Loss SNV dbSNP153 33..33 33 - - - 77682 RMVar_ID_77682 Human_SNP_ID_58696122 m1A Human chr2 - 3448767 3448767 3448767 TGCTCCCGGCACACGCCCTCCGCCCTCGTGTAACCGCGTAACCGGCTGCTCTCCACGCCCTACCC TGCTCCCGGCACACGCCCTCCGCCCTCGTGTAGCCGCGTAACCGGCTGCTCTCCACGCCCTACCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:3448717..3448816;chr2:3448511..3448843 26863196 MeRIP-seq:(Medium) rs942351087 Functional Loss SNV dbSNP153 33..33 33 - - - 77683 RMVar_ID_77683 Human_SNP_ID_58699144 m1A Human chr2 + 3459626 3459626 3459626 AATGTGCAGGGGAGAGCAGGGAGGGACGGGCCAGGCTCAGGGTCGCGGTCAGCCACCGTGTGGCA AATGTGCAGGGGAGAGCAGGGAGGGACGGGCCGGGCTCAGGGTCGCGGTCAGCCACCGTGTGGCA A G TRAPPC12 Ensembl:ENSG00000171853 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3459611..3459687 26863196 MeRIP-seq:(Medium) rs9653595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828556,Human_RBP_ID_18422084,Human_RBP_ID_23282594,Human_RBP_ID_23869306 RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_105260,RMVar_hsa_circ_95742,RMVar_hsa_circ_196700,RMVar_hsa_circ_196701,RMVar_hsa_circ_111176,RMVar_hsa_circ_196709,RMVar_hsa_circ_103367,RMVar_hsa_circ_196702,RMVar_hsa_circ_122158,RMVar_hsa_circ_196705,RMVar_hsa_circ_85576,RMVar_hsa_circ_196707,RMVar_hsa_circ_107998,RMVar_hsa_circ_326994,RMVar_hsa_circ_196710,RMVar_hsa_circ_196711,RMVar_hsa_circ_196708 77684 RMVar_ID_77684 Human_SNP_ID_58699146 m1A Human chr2 - 3459630 3459628 3459631 CTGCTGCCACACGGTGGCTGACCGCGACCCTGAGCCTGGCCCGTCCCTCCCTGCTCTCCCCTGCA CTGCTGCCACACGGTGGCTGACCGCGACCCT___CCTGGCCCGTCCCTCCCTGCTCTCCCCTGCA GCTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3459599..3459880 26863196 MeRIP-seq:(Medium) rs1454297617 Functional Loss DEL dbSNP153 32..34 33 - - - 77685 RMVar_ID_77685 Human_SNP_ID_58710618 m1A Human chr2 - 3499027 3499027 3499027 GTTTGTGGGAGAACCGGTGTGGACAGCGTACAACCGGCCCGCTGACCATTTTGAAGCCCGCGGGC GTTTGTGGGAGAACCGGTGTGGACAGCGTACATCCGGCCCGCTGACCATTTTGAAGCCCGCGGGC T A ADI1 Ensembl:ENSG00000182551 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:3498976..3499100 32194978 MeRIP-seq:(Medium) rs1188667265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8518029,Human_RBP_ID_9383030,Human_RBP_ID_17956093,Human_RBP_ID_23869356 Human_Splice_Rec_213086,Human_Splice_Rec_213092,Human_Splice_Rec_213094 Human_miRNA_ID_2246189,Human_miRNA_ID_2477169,Human_miRNA_ID_2850495 RMVar_hsa_circ_120814,RMVar_hsa_circ_196716 77686 RMVar_ID_77686 Human_SNP_ID_58716443 m1A Human chr2 + 3519495 3519495 3519495 CGTCCATATACCAGGCCTGCACCATGACGCGCAGTGCGGGTGCCGTGTTCGAACCCAGGGGCCGC CGTCCATATACCAGGCCTGCACCATGACGCGCGGTGCGGGTGCCGTGTTCGAACCCAGGGGCCGC A G AC231981.1 Ensembl:ENSG00000235078 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:3519451..3519525 26863196 MeRIP-seq:(Medium) rs776805509 Functional Loss SNV dbSNP153 33..33 33 - - - 77687 RMVar_ID_77687 Human_SNP_ID_58720088 m1A Human chr2 - 3532214 3532214 3532214 GAGAAATGTTTGCAGACGGAGTGAATGCCTTGAAAGTGCTGCGACCAGGTGCTGACACCCGGAGG GAGAAATGTTTGCAGACGGAGTGAATGCCTTGTAAGTGCTGCGACCAGGTGCTGACACCCGGAGG T A AC108488.1,AC108488.2 Ensembl:ENSG00000242282,Ensembl:ENSG00000286905 lincRNA,Protein coding exon,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:3532170..3532264 32194978 MeRIP-seq:(Medium) rs1009921721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205081,Human_RBP_ID_21933656 Human_Splice_Rec_213100,Human_Splice_Rec_213104,Human_Splice_Rec_213108,Human_Splice_Rec_213110,Human_Splice_Rec_213134,Human_Splice_Rec_213156 77688 RMVar_ID_77688 Human_SNP_ID_58723875 m1A Human chr2 - 3545830 3545830 3545830 CCTGGTCATTCGGGATTTATAGGCAATGAAGAAGCTGACAGATTAGCCAGAGAAGGAGCTAAACA CCTGGTCATTCGGGATTTATAGGCAATGAAGACGCTGACAGATTAGCCAGAGAAGGAGCTAAACA T G AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3545696..3545897 26863196 MeRIP-seq:(Medium) rs781530652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550047,Human_RBP_ID_1023074,Human_RBP_ID_1916663,Human_RBP_ID_6914639,Human_RBP_ID_8201366,Human_RBP_ID_8518054,Human_RBP_ID_9383035,Human_RBP_ID_13869325,Human_RBP_ID_17964371,Human_RBP_ID_26486212 Human_Splice_Rec_213128,Human_Splice_Rec_213148,Human_Splice_Rec_213170,Human_Splice_Rec_213184 RMVar_hsa_circ_70,RMVar_hsa_circ_266840,RMVar_hsa_circ_340457,RMVar_hsa_circ_352644,RMVar_hsa_circ_294063 77689 RMVar_ID_77689 Human_SNP_ID_58723887 m1A Human chr2 + 3545866 3545866 3545866 TCATTGCCTATAAATCCCGAATGACCAGGAACATGCATCTGTTAAGATAAATGTTTTCCTTTTAT TCATTGCCTATAAATCCCGAATGACCAGGAACGTGCATCTGTTAAGATAAATGTTTTCCTTTTAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:3545681..3548037 32194978 MeRIP-seq:(Medium) rs1369390181 Functional Loss SNV dbSNP153 33..33 33 - - - 77690 RMVar_ID_77690 Human_SNP_ID_58724797 m1A Human chr2 + 3549109 3549109 3549109 TTTGTCTGCCGCCCAGGAAGTCTAATGCCTACATTTCTGTTTCAAAACAGTACAAAAGAAAATAA TTTGTCTGCCGCCCAGGAAGTCTAATGCCTACGTTTCTGTTTCAAAACAGTACAAAAGAAAATAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:3548669..3550163 32194978 MeRIP-seq:(Medium) rs186475742 Functional Loss SNV dbSNP153 33..33 33 - - - 77691 RMVar_ID_77691 Human_SNP_ID_58727779 m1A Human chr2 + 3558195 3558195 3558195 CTCCTCACGGCATAGAACATCCCGAACCCGCGAGAGCCGCGGCGGCAGGGCAAGGCGGCCAAGGC CTCCTCACGGCATAGAACATCCCGAACCCGCGGGAGCCGCGGCGGCAGGGCAAGGCGGCCAAGGC A G RNASEH1-AS1 RNACentral:URS00009BBB07 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:3558126..3558295 26863196 MeRIP-seq:(Medium) rs1558463910 Functional Loss SNV dbSNP153 33..33 33 - - - 77692 RMVar_ID_77692 Human_SNP_ID_58727823 m1A Human chr2 + 3558259 3558259 3558259 CGACTCTGTGGGCCAGGAACAGAAGCCAGCTCATCGCTCACTCCCGGCACCGGGAAGCATTTCGA CGACTCTGTGGGCCAGGAACAGAAGCCAGCTCGTCGCTCACTCCCGGCACCGGGAAGCATTTCGA A G RNASEH1-AS1 RNACentral:URS00009BBB07 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3558209..3558299 26863196 MeRIP-seq:(Medium) rs1220283496 Functional Loss SNV dbSNP153 33..33 33 - - - 77693 RMVar_ID_77693 Human_SNP_ID_58728067 m1A Human chr2 + 3558734 3558734 3558734 ACGTGCGGTAACCGCGGCTCCTCGAGAGCTCCAGGGATGCGGATCTACAGTAAGGGCTGTGGCCA ACGTGCGGTAACCGCGGCTCCTCGAGAGCTCCGGGGATGCGGATCTACAGTAAGGGCTGTGGCCA A G RNASEH1-AS1 Ensembl:ENSG00000234171 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:3558684..3558925 26863196 MeRIP-seq:(Medium) rs1050357787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625820,Human_RBP_ID_5099899,Human_RBP_ID_23869453 Human_miRNA_ID_3174672 77694 RMVar_ID_77694 Human_SNP_ID_58733125 m1A Human chr2 - 3575583 3575583 3575583 GAACATGGCTTTCTCCTGGGAGAACTGAAGGCACAGCGGTCAGCGTTACGCGGCCCGGGCTGCAG GAACATGGCTTTCTCCTGGGAGAACTGAAGGCGCAGCGGTCAGCGTTACGCGGCCCGGGCTGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:3575576..3575625 26863196 MeRIP-seq:(Medium) rs768167442 Functional Loss SNV dbSNP153 33..33 33 - - - 77695 RMVar_ID_77695 Human_SNP_ID_58734613 m1A Human chr2 + 3580145 3580145 3580145 TACTCTGACAGCTGTGCACGATGCCATCCTTGAGGACTTGGTCTTCCCAAGCGAAATTGTGGGCA TACTCTGACAGCTGTGCACGATGCCATCCTTGTGGACTTGGTCTTCCCAAGCGAAATTGTGGGCA A T RPS7 Ensembl:ENSG00000171863 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1330571701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_144567,Human_RBP_ID_550063,Human_RBP_ID_13869664,Human_RBP_ID_17658322,Human_RBP_ID_18759918,Human_RBP_ID_26818091 Human_Splice_Rec_213218,Human_Splice_Rec_213230,Human_Splice_Rec_213242,Human_Splice_Rec_213260,Human_Splice_Rec_213272,Human_Splice_Rec_213282,Human_Splice_Rec_213292,Human_Splice_Rec_213306 Human_miRNA_ID_2901954,Human_miRNA_ID_3056720 RMVar_hsa_circ_87624,RMVar_hsa_circ_196720 77696 RMVar_ID_77696 Human_SNP_ID_58770281 m1A Human chr2 - 3703548 3703548 3703548 GGGGCTGCCAGGCGGGCGGAGGCTGCGTGTTGACGCGACCCTGGGCGATTGTGACCGCCTGGCCG GGGGCTGCCAGGCGGGCGGAGGCTGCGTGTTGGCGCGACCCTGGGCGATTGTGACCGCCTGGCCG T C AC010907.1 Ensembl:ENSG00000224661 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:3703527..3703614 26863410 MeRIP-seq:(Medium) rs1008838975 Functional Loss SNV dbSNP153 33..33 33 - - - 77697 RMVar_ID_77697 Human_SNP_ID_59619175 m1A Human chr2 + 6917531 6917516 6917532 GTGCGGGCCGTGCGGGCTGCGCGGGCGCGGGGAGGCGCGGGCGGCAAACTGCGGGCACCCGGCAC GTGCGGGCCGTGCGGGCT________________GCGCGGGCGGCAAACTGCGGGCACCCGGCAC TGCGCGGGCGCGGGGAG T RNF144A Ensembl:ENSG00000151692 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:6917480..6917600 26863196 MeRIP-seq:(Medium) rs527528919 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_4622170,Human_RBP_ID_18422086 Human_Splice_Rec_214861,Human_Splice_Rec_214875 77698 RMVar_ID_77698 Human_SNP_ID_59619194 m1A Human chr2 + 6917562 6917562 6917562 GAGGCGCGGGCGGCAAACTGCGGGCACCCGGCACCCCGCAGCCAGTACCGGGCGGAGGCGTCAGA GAGGCGCGGGCGGCAAACTGCGGGCACCCGGCGCCCCGCAGCCAGTACCGGGCGGAGGCGTCAGA A G RNF144A Ensembl:ENSG00000151692 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:6917515..6917589 26863196 MeRIP-seq:(Medium) rs1178447501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622170,Human_RBP_ID_18422086 Human_Splice_Rec_214861,Human_Splice_Rec_214875 77699 RMVar_ID_77699 Human_SNP_ID_60068217 m1A Human chr2 + 8682115 8682115 8682115 CAGCTAGCTCAGCAGGCGGCAGCGGCGGCCTGAGCTTCAGGGCAGCCAGCTCCCTCCCGGTCTCG CAGCTAGCTCAGCAGGCGGCAGCGGCGGCCTGGGCTTCAGGGCAGCCAGCTCCCTCCCGGTCTCG A G ID2 Ensembl:ENSG00000115738 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:8682051..8682423 26863196 MeRIP-seq:(Medium) rs763895722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243504,Human_RBP_ID_4619412,Human_RBP_ID_8526785,Human_RBP_ID_9330320,Human_RBP_ID_18421682,Human_RBP_ID_22450113,Human_RBP_ID_23888320,Human_RBP_ID_27818170 77700 RMVar_ID_77700 Human_SNP_ID_60068219 m1A Human chr2 - 8682119 8682119 8682119 AAGGCGAGACCGGGAGGGAGCTGGCTGCCCTGAAGCTCAGGCCGCCGCTGCCGCCTGCTGAGCTA AAGGCGAGACCGGGAGGGAGCTGGCTGCCCTGGAGCTCAGGCCGCCGCTGCCGCCTGCTGAGCTA T C ID2-AS1,ID2-AS1:2 RNACentral:URS0000D5BD37,RNACentral:URS0000D5AD9F lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:8682051..8682405 26863196 MeRIP-seq:(Medium) rs753568797 Functional Loss SNV dbSNP153 33..33 33 - - - 77701 RMVar_ID_77701 Human_SNP_ID_60068230 m1A Human chr2 - 8682150 8682132 8682150 GGACTGAAGGCTTTCATGCTGACCGCGAGGGAAGGCGAGACCGGGAGGGAGCTGGCTGCCCTGAA GGACTGAAGGCTTTCATGCTGACCGCGAGGGA__________________GCTGGCTGCCCTGAA CTCCCTCCCGGTCTCGCCT C ID2-AS1,ID2-AS1:2 RNACentral:URS0000D5BD37,RNACentral:URS0000D5AD9F lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:8682108..8682238 26863196 MeRIP-seq:(Medium) rs1558272435 Functional Loss DEL dbSNP153 33..50 33 - - - 77702 RMVar_ID_77702 Human_SNP_ID_60068250 m1A Human chr2 - 8682150 8682149 8682150 GGACTGAAGGCTTTCATGCTGACCGCGAGGGAAGGCGAGACCGGGAGGGAGCTGGCTGCCCTGAA GGACTGAAGGCTTTCATGCTGACCGCGAGGGA_GGCGAGACCGGGAGGGAGCTGGCTGCCCTGAA CT C ID2-AS1,ID2-AS1:2 RNACentral:URS0000D5BD37,RNACentral:URS0000D5AD9F lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:8682108..8682238 26863196 MeRIP-seq:(Medium) rs1203942223 Functional Loss DEL dbSNP153 33..33 33 - - - 77703 RMVar_ID_77703 Human_SNP_ID_60080221 m1A Human chr2 + 8730235 8730235 8730235 TGCCATACAGAACGCTGGATCTCGGTTTACTCAGCCTCTCCCTGTAGCGTCACAGGCTGTGCACT TGCCATACAGAACGCTGGATCTCGGTTTACTCCGCCTCTCCCTGTAGCGTCACAGGCTGTGCACT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:8730186..8730336 32194978 MeRIP-seq:(Medium) rs1316681696 Functional Loss SNV dbSNP153 33..33 33 - - - 77704 RMVar_ID_77704 Human_SNP_ID_60080947 m1A Human chr2 + 8732782 8732782 8732782 CTGCTCCTCCTCACCGCTGCCCTGCCCTGCCCACTCAGTGTTACTCGCTGCCGCCCGCTGTGCCT CTGCTCCTCCTCACCGCTGCCCTGCCCTGCCCGCTCAGTGTTACTCGCTGCCGCCCGCTGTGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:8732776..8732859 26863196 MeRIP-seq:(Medium) rs879640920 Functional Loss SNV dbSNP153 33..33 33 - - - 77705 RMVar_ID_77705 Human_SNP_ID_60081135 m1A Human chr2 + 8733542 8733542 8733542 GCTGAAGTTGAGTGTGTAGGGCGTCTGGCTGGAGAGCTCGGTGTGAGGCAGCTCGTTGTGGGAAG GCTGAAGTTGAGTGTGTAGGGCGTCTGGCTGGGGAGCTCGGTGTGAGGCAGCTCGTTGTGGGAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:8731981..8733543 32194978 MeRIP-seq:(Medium) rs1310173085 Functional Loss SNV dbSNP153 33..33 33 - - - 77706 RMVar_ID_77706 Human_SNP_ID_60085211 m1A Human chr2 + 8750334 8750334 8750334 CCAATACTGATCTGCTCTCTGGCAGCACGAACATCTGAAAGATTCAATCAGACCCCAGAAGGCAA CCAATACTGATCTGCTCTCTGGCAGCACGAACTTCTGAAAGATTCAATCAGACCCCAGAAGGCAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:8750318..8751548 32194978 MeRIP-seq:(Medium) rs755494370 Functional Loss SNV dbSNP153 33..33 33 - - - 77707 RMVar_ID_77707 Human_SNP_ID_60119461 m1A Human chr2 - 8897168 8897167 8897169 GGAATCAGAGAAAAAGAGAGAAAGAGACACAGAAAGTCAAAGAGAGGAAGAGACAGAGACAAAGA GGAATCAGAGAAAAAGAGAGAAAGAGACACA__AAGTCAAAGAGAGGAAGAGACAGAGACAAAGA TTC T MBOAT2 Ensembl:ENSG00000143797 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:8897125..8897257 26863196 MeRIP-seq:(Medium) rs1244664815 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_281524,RMVar_hsa_circ_336489,RMVar_hsa_circ_306945,RMVar_hsa_circ_332549,RMVar_hsa_circ_16291,RMVar_hsa_circ_1590,RMVar_hsa_circ_282584,RMVar_hsa_circ_360631,RMVar_hsa_circ_330229,RMVar_hsa_circ_287442,RMVar_hsa_circ_196792,RMVar_hsa_circ_13331,RMVar_hsa_circ_304148,RMVar_hsa_circ_283738,RMVar_hsa_circ_319830,RMVar_hsa_circ_331687,RMVar_hsa_circ_275359 77708 RMVar_ID_77708 Human_SNP_ID_60119462 m1A Human chr2 - 8897168 8897168 8897168 GGAATCAGAGAAAAAGAGAGAAAGAGACACAGAAAGTCAAAGAGAGGAAGAGACAGAGACAAAGA GGAATCAGAGAAAAAGAGAGAAAGAGACACAGGAAGTCAAAGAGAGGAAGAGACAGAGACAAAGA T C MBOAT2 Ensembl:ENSG00000143797 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:8897125..8897257 26863196 MeRIP-seq:(Medium) rs1017627496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281524,RMVar_hsa_circ_336489,RMVar_hsa_circ_306945,RMVar_hsa_circ_332549,RMVar_hsa_circ_16291,RMVar_hsa_circ_1590,RMVar_hsa_circ_282584,RMVar_hsa_circ_360631,RMVar_hsa_circ_330229,RMVar_hsa_circ_287442,RMVar_hsa_circ_196792,RMVar_hsa_circ_13331,RMVar_hsa_circ_304148,RMVar_hsa_circ_283738,RMVar_hsa_circ_319830,RMVar_hsa_circ_331687,RMVar_hsa_circ_275359 77709 RMVar_ID_77709 Human_SNP_ID_60119493 m1A Human chr2 - 8897232 8897231 8897233 AGTCAGAGAAAGAGAGAGGATGAAAGAGAGACAAAGAAGGAGACAGAGAGGAAGAGACAAAGATG AGTCAGAGAAAGAGAGAGGATGAAAGAGAGA__AAGAAGGAGACAGAGAGGAAGAGACAAAGATG TTG T MBOAT2 Ensembl:ENSG00000143797 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:8897192..8897264 26863196 MeRIP-seq:(Medium) rs1360289285 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_281524,RMVar_hsa_circ_336489,RMVar_hsa_circ_306945,RMVar_hsa_circ_332549,RMVar_hsa_circ_16291,RMVar_hsa_circ_1590,RMVar_hsa_circ_282584,RMVar_hsa_circ_360631,RMVar_hsa_circ_330229,RMVar_hsa_circ_287442,RMVar_hsa_circ_196792,RMVar_hsa_circ_13331,RMVar_hsa_circ_304148,RMVar_hsa_circ_283738,RMVar_hsa_circ_319830,RMVar_hsa_circ_331687,RMVar_hsa_circ_275359 77710 RMVar_ID_77710 Human_SNP_ID_60139017 m1A Human chr2 - 8978096 8978096 8978096 GTAAGGAGCGGAGATTTTATTTTAATCATGGCAGTCTGTAGAATGTTTTAGGGTCTGGGTATTGG GTAAGGAGCGGAGATTTTATTTTAATCATGGCGGTCTGTAGAATGTTTTAGGGTCTGGGTATTGG T C MBOAT2 Ensembl:ENSG00000143797 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:8978093..8978278 26863196 MeRIP-seq:(Medium) rs555833765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13982185 RMVar_hsa_circ_196799,RMVar_hsa_circ_89606,RMVar_hsa_circ_196801,RMVar_hsa_circ_196802,RMVar_hsa_circ_196800 77711 RMVar_ID_77711 Human_SNP_ID_60139020 m1A Human chr2 - 8978117 8978117 8978117 GCCTTGGTCTTTCAGGGCAGAGTAAGGAGCGGAGATTTTATTTTAATCATGGCAGTCTGTAGAAT GCCTTGGTCTTTCAGGGCAGAGTAAGGAGCGGGGATTTTATTTTAATCATGGCAGTCTGTAGAAT T C MBOAT2 Ensembl:ENSG00000143797 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:8978108..8978204 26863196 MeRIP-seq:(Medium) rs1048229501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196799,RMVar_hsa_circ_89606,RMVar_hsa_circ_196801,RMVar_hsa_circ_196802,RMVar_hsa_circ_196800 77712 RMVar_ID_77712 Human_SNP_ID_60197196 m1A Human chr2 - 9207077 9207077 9207077 GGCATCGCCTCGGCGCGAGGGCGCTGGCGCACAGCCGCAGGGGCGCCGCCGCCTCAACTGCCGCA GGCATCGCCTCGGCGCGAGGGCGCTGGCGCACGGCCGCAGGGGCGCCGCCGCCTCAACTGCCGCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9207028..9207134 26863196 MeRIP-seq:(Medium) rs1161430157 Functional Loss SNV dbSNP153 33..33 33 - - - 77713 RMVar_ID_77713 Human_SNP_ID_60198920 m1A Human chr2 + 9213155 9213155 9213155 CATGGGGATAGAAAGTGGTTCTGGAGATCAGGAAACCGAAATCAGGAAAAGCCTCTCTGCAGAGG CATGGGGATAGAAAGTGGTTCTGGAGATCAGGGAACCGAAATCAGGAAAAGCCTCTCTGCAGAGG A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9213151..9213667 26863196 MeRIP-seq:(Medium) rs189384551 Functional Loss SNV dbSNP153 33..33 33 - - - 77714 RMVar_ID_77714 Human_SNP_ID_60207629 m1A Human chr2 - 9250943 9250943 9250943 CATCTTATCTCTGTAAGAAATTGACTTTCACCACGCCTCGTTTCATAGTTCACTGTTTTAAGTTC CATCTTATCTCTGTAAGAAATTGACTTTCACCGCGCCTCGTTTCATAGTTCACTGTTTTAAGTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9250938..9251203 26863196 MeRIP-seq:(Medium) rs938215408 Functional Loss SNV dbSNP153 33..33 33 - - - 77715 RMVar_ID_77715 Human_SNP_ID_60218074 m1A Human chr2 + 9292141 9292141 9292141 AGGTCATCTTTCAGGATCCATGGAATGAAAGGACTCAGCAGTGAGTATAGCAGCCCTGAGGAGGT AGGTCATCTTTCAGGATCCATGGAATGAAAGGTCTCAGCAGTGAGTATAGCAGCCCTGAGGAGGT A T ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9292136..9292244 26863196 MeRIP-seq:(Medium) rs1049914959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4650,RMVar_hsa_circ_111752,RMVar_hsa_circ_270930,RMVar_hsa_circ_372788,RMVar_hsa_circ_122057,RMVar_hsa_circ_196811,RMVar_hsa_circ_2175,RMVar_hsa_circ_4128,RMVar_hsa_circ_196812,RMVar_hsa_circ_196813,RMVar_hsa_circ_196809,RMVar_hsa_circ_196810 77716 RMVar_ID_77716 Human_SNP_ID_60221053 m1A Human chr2 + 9304579 9304579 9304579 TGCAGTTGTGGGGGTGTAGATACAGGGTGGAGAGGCTGTAGTCTTGGGAGTATAGATATTGGTGG TGCAGTTGTGGGGGTGTAGATACAGGGTGGAGGGGCTGTAGTCTTGGGAGTATAGATATTGGTGG A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9304531..9304664 26863196 MeRIP-seq:(Medium) rs987105030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200308,Human_RBP_ID_18947561 RMVar_hsa_circ_4650,RMVar_hsa_circ_111752,RMVar_hsa_circ_372788,RMVar_hsa_circ_122057,RMVar_hsa_circ_48571,RMVar_hsa_circ_196811,RMVar_hsa_circ_2175,RMVar_hsa_circ_4128,RMVar_hsa_circ_196812,RMVar_hsa_circ_196813,RMVar_hsa_circ_196810,RMVar_hsa_circ_292004,RMVar_hsa_circ_27677,RMVar_hsa_circ_43688,RMVar_hsa_circ_7007,RMVar_hsa_circ_196814,RMVar_hsa_circ_196815 77717 RMVar_ID_77717 Human_SNP_ID_60221058 m1A Human chr2 - 9304590 9304590 9304590 CTCCAGCCTCTCCACCAATATCTATACTCCCAAGACTACAGCCTCTCCACCCTGTATCTACACCC CTCCAGCCTCTCCACCAATATCTATACTCCCAGGACTACAGCCTCTCCACCCTGTATCTACACCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:9304501..9304630 26863196 MeRIP-seq:(Medium) rs183978242 Functional Loss SNV dbSNP153 33..33 33 - - - 77718 RMVar_ID_77718 Human_SNP_ID_60221150 m1A Human chr2 + 9304817 9304817 9304817 GGGCTGGAGTAGTGAGGTATAGATATTGGTGGAGGGGCTGGACGAGTGGGGTGTAGATATTGGTG GGGCTGGAGTAGTGAGGTATAGATATTGGTGGGGGGGCTGGACGAGTGGGGTGTAGATATTGGTG A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:9304798..9305074 26863196 MeRIP-seq:(Medium) rs1331790523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4650,RMVar_hsa_circ_111752,RMVar_hsa_circ_372788,RMVar_hsa_circ_122057,RMVar_hsa_circ_48571,RMVar_hsa_circ_196811,RMVar_hsa_circ_2175,RMVar_hsa_circ_4128,RMVar_hsa_circ_196812,RMVar_hsa_circ_196813,RMVar_hsa_circ_196810,RMVar_hsa_circ_292004,RMVar_hsa_circ_27677,RMVar_hsa_circ_43688,RMVar_hsa_circ_7007,RMVar_hsa_circ_196814,RMVar_hsa_circ_196815 77719 RMVar_ID_77719 Human_SNP_ID_60221319 m1A Human chr2 - 9305277 9305277 9305277 CCCACTACTACAGCCTCTACACCAACATCTATACCCCACTATTACAGCCCCTCCACCAATATGTA CCCACTACTACAGCCTCTACACCAACATCTATGCCCCACTATTACAGCCCCTCCACCAATATGTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9304780..9305534 26863196 MeRIP-seq:(Medium) rs1288299141 Functional Loss SNV dbSNP153 33..33 33 - - - 77720 RMVar_ID_77720 Human_SNP_ID_60221505 m1A Human chr2 + 9305694 9305694 9305694 GGGCTGTAATAGTGGGGTATAGATATTGGTGGAGAGGCTGTAGTAGTGGGGTATAGATATTGGTG GGGCTGTAATAGTGGGGTATAGATATTGGTGGTGAGGCTGTAGTAGTGGGGTATAGATATTGGTG A T ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:9305684..9305963 26863196 MeRIP-seq:(Medium) rs1191084465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4650,RMVar_hsa_circ_111752,RMVar_hsa_circ_372788,RMVar_hsa_circ_122057,RMVar_hsa_circ_48571,RMVar_hsa_circ_196811,RMVar_hsa_circ_2175,RMVar_hsa_circ_4128,RMVar_hsa_circ_196812,RMVar_hsa_circ_196813,RMVar_hsa_circ_196810,RMVar_hsa_circ_292004,RMVar_hsa_circ_27677,RMVar_hsa_circ_43688,RMVar_hsa_circ_7007,RMVar_hsa_circ_196814,RMVar_hsa_circ_196815 77721 RMVar_ID_77721 Human_SNP_ID_60221515 m1A Human chr2 + 9305730 9305730 9305730 GCTGTAGTAGTGGGGTATAGATATTGGTGGAGAGGCTGTAGTAGTGGGGTATAGATATTGGTGGA GCTGTAGTAGTGGGGTATAGATATTGGTGGAGGGGCTGTAGTAGTGGGGTATAGATATTGGTGGA A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9305632..9306037 26863196 MeRIP-seq:(Medium) rs1426929871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4650,RMVar_hsa_circ_111752,RMVar_hsa_circ_372788,RMVar_hsa_circ_122057,RMVar_hsa_circ_48571,RMVar_hsa_circ_196811,RMVar_hsa_circ_2175,RMVar_hsa_circ_4128,RMVar_hsa_circ_196812,RMVar_hsa_circ_196813,RMVar_hsa_circ_196810,RMVar_hsa_circ_292004,RMVar_hsa_circ_27677,RMVar_hsa_circ_43688,RMVar_hsa_circ_7007,RMVar_hsa_circ_196814,RMVar_hsa_circ_196815 77722 RMVar_ID_77722 Human_SNP_ID_60221835 m1A Human chr2 - 9306635 9306635 9306635 GACTCCTGGCTGGGCTCATCAACCCGAGGACAAAGGGGCACAGGATCTCCACAGCTCACAGCCCC GACTCCTGGCTGGGCTCATCAACCCGAGGACAGAGGGGCACAGGATCTCCACAGCTCACAGCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9306591..9306682 26863196 MeRIP-seq:(Medium) rs961091936 Functional Loss SNV dbSNP153 33..33 33 - - - 77723 RMVar_ID_77723 Human_SNP_ID_60250251 m1A Human chr2 - 9418714 9418714 9418714 ATTTGTTTTTTCAGGGGATCTTCTCTGGATCAAGCAATGGTGGTGAAAAATGTTTCGCAAGGGCA ATTTGTTTTTTCAGGGGATCTTCTCTGGATCAGGCAATGGTGGTGAAAAATGTTTCGCAAGGGCA T C ITGB1BP1 Ensembl:ENSG00000119185 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9418651..9420108 26863196 MeRIP-seq:(Medium) rs757006502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58347,Human_RBP_ID_557651,Human_RBP_ID_922456,Human_RBP_ID_1591479,Human_RBP_ID_1924787,Human_RBP_ID_4623091,Human_RBP_ID_9113155,Human_RBP_ID_9383056,Human_RBP_ID_22547017 Human_Splice_Rec_216172,Human_Splice_Rec_216173,Human_Splice_Rec_216184,Human_Splice_Rec_216185,Human_Splice_Rec_216194,Human_Splice_Rec_216195,Human_Splice_Rec_216206,Human_Splice_Rec_216207,Human_Splice_Rec_216230,Human_Splice_Rec_216231,Human_Splice_Rec_216248,Human_Splice_Rec_216249,Human_Splice_Rec_216260,Human_Splice_Rec_216261,Human_Splice_Rec_216272,Human_Splice_Rec_216273,Human_Splice_Rec_216292,Human_Splice_Rec_216293,Human_Splice_Rec_216310,Human_Splice_Rec_216311,Human_Splice_Rec_216318,Human_Splice_Rec_216319,Human_Splice_Rec_216326,Human_Splice_Rec_216327,Human_Splice_Rec_216332,Human_Splice_Rec_216333,Human_Splice_Rec_216338,Human_Splice_Rec_216339 Human_miRNA_ID_2170793 RMVar_hsa_circ_311960,RMVar_hsa_circ_196850,RMVar_hsa_circ_301507,RMVar_hsa_circ_196851,RMVar_hsa_circ_325953,RMVar_hsa_circ_271814,RMVar_hsa_circ_196852,RMVar_hsa_circ_196853,RMVar_hsa_circ_196856,RMVar_hsa_circ_295178,RMVar_hsa_circ_347021,RMVar_hsa_circ_94444,RMVar_hsa_circ_196855,RMVar_hsa_circ_347887 77724 RMVar_ID_77724 Human_SNP_ID_60251339 m1A Human chr2 - 9423468 9423468 9423468 GTGGGCAGGAGGGCTGGAAAAGCCGGCGCTGGAGCGGGAACGGGAGTAGCTGCCTGGGCGCCAAA GTGGGCAGGAGGGCTGGAAAAGCCGGCGCTGGGGCGGGAACGGGAGTAGCTGCCTGGGCGCCAAA T C ITGB1BP1 Ensembl:ENSG00000119185 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:9423333..9423544;chr2:9423339..9423500;chr2:9423320..9423575;chr2:9423238..9423575;chr2:9423347..9423575 26863196 MeRIP-seq:(Medium) rs1308703442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4619979,Human_RBP_ID_6957297,Human_RBP_ID_22450997 Human_Splice_Rec_216183,Human_Splice_Rec_216193,Human_Splice_Rec_216205,Human_Splice_Rec_216215,Human_Splice_Rec_216223,Human_Splice_Rec_216229,Human_Splice_Rec_216257,Human_Splice_Rec_216271,Human_Splice_Rec_216301 77725 RMVar_ID_77725 Human_SNP_ID_60251450 m1A Human chr2 + 9423726 9423726 9423726 TTTACCGGTGGCTGTGCTTCCAATTTAGGAAGACCCCGGCGACCTGTTCCTCACCCCCGCTTCGC TTTACCGGTGGCTGTGCTTCCAATTTAGGAAGTCCCCGGCGACCTGTTCCTCACCCCCGCTTCGC A T CPSF3 Ensembl:ENSG00000119203 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:9423682..9423776 26863196 MeRIP-seq:(Medium) rs777029355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778070,Human_RBP_ID_4623987,Human_RBP_ID_5471148,Human_RBP_ID_8851013,Human_RBP_ID_9330906,Human_RBP_ID_17509241,Human_RBP_ID_17963060,Human_RBP_ID_24422048 Human_Splice_Rec_216351 77726 RMVar_ID_77726 Human_SNP_ID_60268556 m1A Human chr2 - 9489238 9489238 9489238 AAAAAAAAAAATTCACTATCTACAAACCTAGAATATTTAAAATACAAAGATTGCCTGTTTTCAAA AAAAAAAAAAATTCACTATCTACAAACCTAGACTATTTAAAATACAAAGATTGCCTGTTTTCAAA T G ADAM17 Ensembl:ENSG00000151694 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13008101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557803,Human_RBP_ID_22394295 77727 RMVar_ID_77727 Human_SNP_ID_60284142 m1A Human chr2 + 9552580 9552580 9552580 GGAGAATCCCCATGCCAATAACCTCAAGGTAAATTTGAAAATACATGTTTCAGATACAAACTTTC GGAGAATCCCCATGCCAATAACCTCAAGGTAAGTTTGAAAATACATGTTTCAGATACAAACTTTC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:9552559..9552641 26863410 MeRIP-seq:(Medium) rs947799313 Functional Loss SNV dbSNP153 33..33 33 - - - 77728 RMVar_ID_77728 Human_SNP_ID_60284839 m1A Human chr2 + 9555190 9555190 9555190 AAGGCAAGAACCCTGACCACATCTCCCTCTCCAAACAAGATCCAGCCACCCTACTCCTTACCGCT AAGGCAAGAACCCTGACCACATCTCCCTCTCCCAACAAGATCCAGCCACCCTACTCCTTACCGCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9555157..9555492 26863196 MeRIP-seq:(Medium) rs1213447188 Functional Loss SNV dbSNP153 33..33 33 - - - 77729 RMVar_ID_77729 Human_SNP_ID_60284979 m1A Human chr2 + 9555604 9555604 9555604 CCACGCTGGTCAGGAATAGGAGAGACTGCCTCATGTTCCCGGCCCCGCTACCGACTCCACCTCTC CCACGCTGGTCAGGAATAGGAGAGACTGCCTCCTGTTCCCGGCCCCGCTACCGACTCCACCTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:9555553..9555775 26863196 MeRIP-seq:(Medium) rs1412029115 Functional Loss SNV dbSNP153 33..33 33 - - - 77730 RMVar_ID_77730 Human_SNP_ID_60285026 m1A Human chr2 + 9555716 9555716 9555716 GGAGGACGGGATCCGCCCGGCCTAGCCCCTCAATCCTCTTTTCCCTCCCGCGCCGCCTACTGGGA GGAGGACGGGATCCGCCCGGCCTAGCCCCTCAGTCCTCTTTTCCCTCCCGCGCCGCCTACTGGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9555587..9555756 26863196 MeRIP-seq:(Medium) rs1215221437 Functional Loss SNV dbSNP153 33..33 33 - - - 77731 RMVar_ID_77731 Human_SNP_ID_60292645 m1A Human chr2 + 9585328 9585328 9585328 GCCCCTTCTGCCGCATCACATTCTTCTCCTGCACTGTCTGATGTCCAAAGCTAGAAAAAGAAGAA GCCCCTTCTGCCGCATCACATTCTTCTCCTGCGCTGTCTGATGTCCAAAGCTAGAAAAAGAAGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:9585277..9585373 26863196 MeRIP-seq:(Medium) rs775943040 Functional Loss SNV dbSNP153 33..33 33 - - - 77732 RMVar_ID_77732 Human_SNP_ID_60304647 m1A Human chr2 - 9630275 9630275 9630275 AGAACGTGGTCGGGGGCCGCAGGTCCGCCTGGAGGGTCATCTCTAGCATCGAGCAGAAGACCGAC AGAACGTGGTCGGGGGCCGCAGGTCCGCCTGGGGGGTCATCTCTAGCATCGAGCAGAAGACCGAC T C YWHAQ Ensembl:ENSG00000134308 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:9630176..9630276 32194978 MeRIP-seq:(Medium) rs1410406554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242749,Human_RBP_ID_558377,Human_RBP_ID_775650,Human_RBP_ID_923514,Human_RBP_ID_1591958,Human_RBP_ID_4621571,Human_RBP_ID_6959848,Human_RBP_ID_9330328,Human_RBP_ID_9383066,Human_RBP_ID_22450116,Human_RBP_ID_23890524,Human_RBP_ID_26338447,Human_RBP_ID_26818119 Human_miRNA_ID_2064325,Human_miRNA_ID_2364990,Human_miRNA_ID_2702202,Human_miRNA_ID_2933506 RMVar_hsa_circ_79062,RMVar_hsa_circ_96841,RMVar_hsa_circ_196910,RMVar_hsa_circ_196911 77733 RMVar_ID_77733 Human_SNP_ID_60304790 m1A Human chr2 + 9630490 9630490 9630490 GCGCGGGGCCGGGGCCGGGGCGGAGGGCGAGGAGAGCGAGGGCGAGCGCCGACCCGCAGCGGGAG GCGCGGGGCCGGGGCCGGGGCGGAGGGCGAGGGGAGCGAGGGCGAGCGCCGACCCGCAGCGGGAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:9630225..9630600 26863410 MeRIP-seq:(Medium) rs1039329287 Functional Loss SNV dbSNP153 33..33 33 - - - 77734 RMVar_ID_77734 Human_SNP_ID_60304803 m1A Human chr2 + 9630502 9630502 9630502 GGCCGGGGCGGAGGGCGAGGAGAGCGAGGGCGAGCGCCGACCCGCAGCGGGAGGAGCCTCGAGAG GGCCGGGGCGGAGGGCGAGGAGAGCGAGGGCGGGCGCCGACCCGCAGCGGGAGGAGCCTCGAGAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr2:9630405..9630550;chr2:9630401..9630575 26863196,26863410 MeRIP-seq:(Medium) rs1403693179 Functional Loss SNV dbSNP153 33..33 33 - - - 77735 RMVar_ID_77735 Human_SNP_ID_60305012 m1A Human chr2 + 9630931 9630931 9630931 AGCGCGGCCGGAGGAAGCCCGCGGGCCGACCCAGGCGCTCACCTTCACGTCTCCGCGGCCGCGAC AGCGCGGCCGGAGGAAGCCCGCGGGCCGACCCGGGCGCTCACCTTCACGTCTCCGCGGCCGCGAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr2:9630926..9631000;chr2:9630926..9631025 26863196,26863410 MeRIP-seq:(Medium) rs1260861298 Functional Loss SNV dbSNP153 33..33 33 - - - 77736 RMVar_ID_77736 Human_SNP_ID_60305019 m1A Human chr2 + 9630945 9630945 9630945 AAGCCCGCGGGCCGACCCAGGCGCTCACCTTCACGTCTCCGCGGCCGCGACGCGAGTCCCACCAC AAGCCCGCGGGCCGACCCAGGCGCTCACCTTCCCGTCTCCGCGGCCGCGACGCGAGTCCCACCAC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:9630926..9631025 26863410 MeRIP-seq:(Medium) rs1366784041 Functional Loss SNV dbSNP153 33..33 33 - - - 77737 RMVar_ID_77737 Human_SNP_ID_60305020 m1A Human chr2 + 9630945 9630945 9630945 AAGCCCGCGGGCCGACCCAGGCGCTCACCTTCACGTCTCCGCGGCCGCGACGCGAGTCCCACCAC AAGCCCGCGGGCCGACCCAGGCGCTCACCTTCGCGTCTCCGCGGCCGCGACGCGAGTCCCACCAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:9630926..9631025 26863410 MeRIP-seq:(Medium) rs1366784041 Functional Loss SNV dbSNP153 33..33 33 - - - 77738 RMVar_ID_77738 Human_SNP_ID_60359560 m1A Human chr2 + 9843671 9843671 9843671 CCGCGGGTTGGGGCGGCGACGCCACCGGCTGGAGGAAGGCGGGGCGGAGGGCTGCAGGGCGGGCT CCGCGGGTTGGGGCGGCGACGCCACCGGCTGGGGGAAGGCGGGGCGGAGGGCTGCAGGGCGGGCT A G TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:9843522..9843823 26863196 MeRIP-seq:(Medium) rs1055394731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5380531 Human_Splice_Rec_217095 77739 RMVar_ID_77739 Human_SNP_ID_60363796 m1A Human chr2 + 9860758 9860758 9860758 GAGGGCAGTGATCAGCTGTGATAAATGCTGTCACTAGGTCAAGAAGGAAGAGGGCTGCAAAGTGG GAGGGCAGTGATCAGCTGTGATAAATGCTGTCGCTAGGTCAAGAAGGAAGAGGGCTGCAAAGTGG A G TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:9860752..9860817 26863196 MeRIP-seq:(Medium) rs775459912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8469,RMVar_hsa_circ_16824,RMVar_hsa_circ_370697,RMVar_hsa_circ_277698,RMVar_hsa_circ_50264,RMVar_hsa_circ_196913,RMVar_hsa_circ_334175,RMVar_hsa_circ_348640,RMVar_hsa_circ_196912,RMVar_hsa_circ_334375,RMVar_hsa_circ_307805,RMVar_hsa_circ_196916,RMVar_hsa_circ_10137,RMVar_hsa_circ_196917,RMVar_hsa_circ_8061 77740 RMVar_ID_77740 Human_SNP_ID_60363797 m1A Human chr2 + 9860758 9860758 9860758 GAGGGCAGTGATCAGCTGTGATAAATGCTGTCACTAGGTCAAGAAGGAAGAGGGCTGCAAAGTGG GAGGGCAGTGATCAGCTGTGATAAATGCTGTCTCTAGGTCAAGAAGGAAGAGGGCTGCAAAGTGG A T TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:9860752..9860817 26863196 MeRIP-seq:(Medium) rs775459912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8469,RMVar_hsa_circ_16824,RMVar_hsa_circ_370697,RMVar_hsa_circ_277698,RMVar_hsa_circ_50264,RMVar_hsa_circ_196913,RMVar_hsa_circ_334175,RMVar_hsa_circ_348640,RMVar_hsa_circ_196912,RMVar_hsa_circ_334375,RMVar_hsa_circ_307805,RMVar_hsa_circ_196916,RMVar_hsa_circ_10137,RMVar_hsa_circ_196917,RMVar_hsa_circ_8061 77741 RMVar_ID_77741 Human_SNP_ID_60386414 m1A Human chr2 - 9951732 9951732 9951732 GGAGGAGGCGGCGGCGGCGGCTGCGGGTCCGGAGCGGCGGCCCCGACGGGTTGGGTTTGCTTTTC GGAGGAGGCGGCGGCGGCGGCTGCGGGTCCGGGGCGGCGGCCCCGACGGGTTGGGTTTGCTTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9951722..9951879 26863196 MeRIP-seq:(Medium) rs1051770129 Functional Loss SNV dbSNP153 33..33 33 - - - 77742 RMVar_ID_77742 Human_SNP_ID_60386415 m1A Human chr2 - 9951732 9951732 9951732 GGAGGAGGCGGCGGCGGCGGCTGCGGGTCCGGAGCGGCGGCCCCGACGGGTTGGGTTTGCTTTTC GGAGGAGGCGGCGGCGGCGGCTGCGGGTCCGGCGCGGCGGCCCCGACGGGTTGGGTTTGCTTTTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9951722..9951879 26863196 MeRIP-seq:(Medium) rs1051770129 Functional Loss SNV dbSNP153 33..33 33 - - - 77743 RMVar_ID_77743 Human_SNP_ID_60401649 m1A Human chr2 + 10011065 10011065 10011065 GGCAGGCGTGCGTACAGGCGGGTCAGGTGGGCAGGCGTTTGTATGGGCGGGTCAGGTGGGCAGGC GGCAGGCGTGCGTACAGGCGGGTCAGGTGGGCGGGCGTTTGTATGGGCGGGTCAGGTGGGCAGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10010980..10011064 26863196 MeRIP-seq:(Medium) rs375002763 Functional Loss SNV dbSNP153 33..33 33 - - - 77744 RMVar_ID_77744 Human_SNP_ID_60402637 m1A Human chr2 + 10012665 10012665 10012665 CGTATGGGCGGGTCAGGTGGACAGGCATGTGTATGGGCGGGTCAGGTGGACAGACGTGCGTATGG CGTATGGGCGGGTCAGGTGGACAGGCATGTGTGTGGGCGGGTCAGGTGGACAGACGTGCGTATGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10012647..10012733 26863196 MeRIP-seq:(Medium) rs1212586767 Functional Loss SNV dbSNP153 33..33 33 - - - 77745 RMVar_ID_77745 Human_SNP_ID_60412569 m1A Human chr2 - 10043699 10043699 10043699 GTCCGGCGTGTGCATCGTGCAGGCCGGCCGGGAGCAACAAAGCGGCCGCGGGGCGTGAGCTCGGG GTCCGGCGTGTGCATCGTGCAGGCCGGCCGGGGGCAACAAAGCGGCCGCGGGGCGTGAGCTCGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10043604..10043876 26863196 MeRIP-seq:(Medium) rs1293497080 Functional Loss SNV dbSNP153 33..33 33 - - - 77746 RMVar_ID_77746 Human_SNP_ID_60412588 m1A Human chr2 + 10043717 10043717 10043717 GGCCGCTTTGTTGCTCCCGGCCGGCCTGCACGATGCACACGCCGGACTTCGCAGGCCCAGACGAC GGCCGCTTTGTTGCTCCCGGCCGGCCTGCACGGTGCACACGCCGGACTTCGCAGGCCCAGACGAC A G KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10043581..10046185 26863196 MeRIP-seq:(Medium) rs1479413677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623101,Human_RBP_ID_5469699 Human_Splice_Rec_217285 77747 RMVar_ID_77747 Human_SNP_ID_60412604 m1A Human chr2 + 10043737 10043737 10043737 CCGGCCTGCACGATGCACACGCCGGACTTCGCAGGCCCAGACGACGCGCGCGCAGTGAGTGGTGG CCGGCCTGCACGATGCACACGCCGGACTTCGCCGGCCCAGACGACGCGCGCGCAGTGAGTGGTGG A C KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr2:10043581..10043775;chr2:10043585..10046185 26863196 MeRIP-seq:(Medium) rs971191887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_217285 77748 RMVar_ID_77748 Human_SNP_ID_60412957 m1A Human chr2 + 10044256 10044256 10044256 CCTGGGGGCGGGCAAGGTCTAGGGGCCGGGGCAACGACGGGAGGCGGGAGCGCCGCACTGCCTTG CCTGGGGGCGGGCAAGGTCTAGGGGCCGGGGCGACGACGGGAGGCGGGAGCGCCGCACTGCCTTG A G KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10044249..10044436 26863196 MeRIP-seq:(Medium) rs1473084472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264152,Human_RBP_ID_3637839,Human_RBP_ID_5321987,Human_RBP_ID_9330335,Human_RBP_ID_18493167,Human_RBP_ID_19104463,Human_RBP_ID_26786754 77749 RMVar_ID_77749 Human_SNP_ID_60414689 m1A Human chr2 + 10048427 10048427 10048427 CCTGTGCAGCCAATGTCATGGCTGCCGGGAATACCAAGTTGTTGCCCCTTGCCCCTGCTCCAGTG CCTGTGCAGCCAATGTCATGGCTGCCGGGAATGCCAAGTTGTTGCCCCTTGCCCCTGCTCCAGTG A G KLF11 Ensembl:ENSG00000172059 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10048377..10048448 26863196 MeRIP-seq:(Medium) rs946559025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1019558,Human_RBP_ID_6808916,Human_RBP_ID_8840855,Human_RBP_ID_9294665,Human_RBP_ID_17273111 RMVar_hsa_circ_288273 77750 RMVar_ID_77750 Human_SNP_ID_60416767 m1A Human chr2 - 10054719 10054717 10054720 AAACATAATTATGAAACATTTTAAGTCTTATCATTCAAACTACTTAAAAGGCTCAAAGTCACAAA AAACATAATTATGAAACATTTTAAGTCTTAT___TCAAACTACTTAAAAGGCTCAAAGTCACAAA AATG A AC104794.5 Ensembl:ENSG00000271787 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:10054469..10054718 32194978 MeRIP-seq:(Medium) rs1238207407 Functional Loss DEL dbSNP153 32..34 33 - - - 77751 RMVar_ID_77751 Human_SNP_ID_60435425 m1A Human chr2 - 10122777 10122777 10122777 AGGGAGAGCATAGTGGAGGCGCAGCGAAGCAGAGCGAGCAGCCAGGACAGGACGGCTGGGACAGG AGGGAGAGCATAGTGGAGGCGCAGCGAAGCAGGGCGAGCAGCCAGGACAGGACGGCTGGGACAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10122726..10123000 26863196 MeRIP-seq:(Medium) rs772043963 Functional Loss SNV dbSNP153 33..33 33 - - - 77752 RMVar_ID_77752 Human_SNP_ID_60435465 m1A Human chr2 + 10122836 10122836 10122836 CTCCCTCCGTGTCCCGCTCGCGCCCATCACGGACCCGCAGCAGCTGCAGCTCTCGCCGCTGAAGG CTCCCTCCGTGTCCCGCTCGCGCCCATCACGGGCCCGCAGCAGCTGCAGCTCTCGCCGCTGAAGG A G RRM2 Ensembl:ENSG00000171848 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:10122726..10123502 26863410 MeRIP-seq:(Medium) rs778032057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8840926,Human_RBP_ID_27473894 Human_Splice_Rec_217324,Human_Splice_Rec_217325,Human_Splice_Rec_217343,Human_Splice_Rec_217361,Human_Splice_Rec_217379,Human_Splice_Rec_217385,Human_Splice_Rec_217403,Human_Splice_Rec_217411,Human_Splice_Rec_217429,Human_Splice_Rec_217451 RMVar_hsa_circ_14519 77753 RMVar_ID_77753 Human_SNP_ID_60437314 m1A Human chr2 + 10129430 10129430 10129430 ATGTGCCCTTACTTGGCTGATTTTTTTTTTCCATCTCATAAGAAAAATCAGCTGAAGTGTTACCA ATGTGCCCTTACTTGGCTGATTTTTTTTTTCCTTCTCATAAGAAAAATCAGCTGAAGTGTTACCA A T RRM2 Ensembl:ENSG00000171848 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:10129379..10129479 32194978 MeRIP-seq:(Medium) rs772288724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60256,Human_RBP_ID_531023,Human_RBP_ID_4626059,Human_RBP_ID_6809574,Human_RBP_ID_8497918,Human_RBP_ID_8840942,Human_RBP_ID_17273143,Human_RBP_ID_17502921,Human_RBP_ID_17966472,Human_RBP_ID_18193452,Human_RBP_ID_18308594,Human_RBP_ID_22241913,Human_RBP_ID_23211877,Human_RBP_ID_24485633,Human_RBP_ID_26818131,Human_RBP_ID_27473901,Human_RBP_ID_27685194 Human_miRNA_ID_301984,Human_miRNA_ID_1382093 RMVar_hsa_circ_65270,RMVar_hsa_circ_117641,RMVar_hsa_circ_116289,RMVar_hsa_circ_196934,RMVar_hsa_circ_196937,RMVar_hsa_circ_121289,RMVar_hsa_circ_125555,RMVar_hsa_circ_196938,RMVar_hsa_circ_196939 77754 RMVar_ID_77754 Human_SNP_ID_60452863 m1A Human chr2 + 10190581 10190581 10190581 TGAGGATGGTGGTGGTGATGATGGTGATGATCATGGTGATGGTGGTGATGTTGGCGATGATGGTG TGAGGATGGTGGTGGTGATGATGGTGATGATCGTGGTGATGGTGGTGATGTTGGCGATGATGGTG A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10189908..10190627 26863196 MeRIP-seq:(Medium) rs111163325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5651826,Human_RBP_ID_8110132,Human_RBP_ID_22743167 77755 RMVar_ID_77755 Human_SNP_ID_60452864 m1A Human chr2 + 10190581 10190581 10190581 TGAGGATGGTGGTGGTGATGATGGTGATGATCATGGTGATGGTGGTGATGTTGGCGATGATGGTG TGAGGATGGTGGTGGTGATGATGGTGATGATCTTGGTGATGGTGGTGATGTTGGCGATGATGGTG A T RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10189908..10190627 26863196 MeRIP-seq:(Medium) rs111163325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5651826,Human_RBP_ID_8110132,Human_RBP_ID_22743167 77756 RMVar_ID_77756 Human_SNP_ID_60452922 m1A Human chr2 + 10190737 10190737 10190737 TTACAATGCTGAGAGTGATGATCTTGGCGGTGATGGTGGTGATGTTGGCGATGATGGTGGTAATG TTACAATGCTGAGAGTGATGATCTTGGCGGTGGTGGTGGTGATGTTGGCGATGATGGTGGTAATG A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10190686..10190768 26863196 MeRIP-seq:(Medium) rs112455259 Functional Loss SNV dbSNP153 33..33 33 - - - 77757 RMVar_ID_77757 Human_SNP_ID_60454814 m1A Human chr2 - 10198178 10198178 10198178 CTCTGATGATTGTCCTGCTGAAGATGCACCCCATGGGTGGGGCTCCCCTGAAGCCTGTGCATAGC CTCTGATGATTGTCCTGCTGAAGATGCACCCCCTGGGTGGGGCTCCCCTGAAGCCTGTGCATAGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:10198133..10198235 32194978 MeRIP-seq:(Medium) rs377654698 Functional Loss SNV dbSNP153 33..33 33 - - - 77758 RMVar_ID_77758 Human_SNP_ID_60457538 m1A Human chr2 + 10208219 10208219 10208219 GAAGCCGAAGGGACAGCAAGTGGGTAGATGGCAGGTGACTGGCCCCAGGTTATCCAGAGCAGAGC GAAGCCGAAGGGACAGCAAGTGGGTAGATGGCGGGTGACTGGCCCCAGGTTATCCAGAGCAGAGC A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:10208126..10208314 26863196 MeRIP-seq:(Medium) rs1471202967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5593437,Human_RBP_ID_6810102 77759 RMVar_ID_77759 Human_SNP_ID_60458841 m1A Human chr2 + 10213097 10213097 10213097 GGGAAGGAAGGAAGGAAAAGAAAATAAAAGGAAAAAAGAAAGAAAGAAAAGAAAAGAAAGGAAGG GGGAAGGAAGGAAGGAAAAGAAAATAAAAGGAGAAAAGAAAGAAAGAAAAGAAAAGAAAGGAAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10213047..10213126 26863196 MeRIP-seq:(Medium) rs1317368613 Functional Loss SNV dbSNP153 33..33 33 - - - 77760 RMVar_ID_77760 Human_SNP_ID_60458849 m1A Human chr2 + 10213105 10213103 10213106 AGGAAGGAAAAGAAAATAAAAGGAAAAAAGAAAGAAAGAAAAGAAAAGAAAGGAAGGAAAGAGAG AGGAAGGAAAAGAAAATAAAAGGAAAAAAGA___AAAGAAAAGAAAAGAAAGGAAGGAAAGAGAG AAAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10212890..10213145 26863196 MeRIP-seq:(Medium) rs1233318188 Functional Loss DEL dbSNP153 32..34 33 - - - 77761 RMVar_ID_77761 Human_SNP_ID_60459694 m1A Human chr2 + 10216090 10216086 10216090 GAAGGAAGGAAGGAAAGAAGGAAGGAAGGAAAAGGAAGGAAGGAAGAGGAAAGGAAGGAAGGAGG GAAGGAAGGAAGGAAAGAAGGAAGGAAGG____GGAAGGAAGGAAGAGGAAAGGAAGGAAGGAGG GAAAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10215976..10216230 26863196 MeRIP-seq:(Medium) rs1192217297 Functional Loss DEL dbSNP153 30..33 33 - - - 77762 RMVar_ID_77762 Human_SNP_ID_60459695 m1A Human chr2 + 10216090 10216087 10216091 GAAGGAAGGAAGGAAAGAAGGAAGGAAGGAAAAGGAAGGAAGGAAGAGGAAAGGAAGGAAGGAGG GAAGGAAGGAAGGAAAGAAGGAAGGAAGGA____GAAGGAAGGAAGAGGAAAGGAAGGAAGGAGG AAAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10215976..10216230 26863196 MeRIP-seq:(Medium) rs758374055 Functional Loss DEL dbSNP153 31..34 33 - - - 77763 RMVar_ID_77763 Human_SNP_ID_60483416 m1A Human chr2 + 10303115 10303071 10303115 GCTTGTCCCGGGCAGCGGCCCGGGCCCGCTGCAGCCGCCGCCGGCGCCGAACTTGGGCTCGGGAA _________________________________GCCGCCGCCGGCGCCGAACTTGGGCTCGGGAA CGGCCTCGGCGCGCTTGTCCCGGGCAGCGGCCCGGGCCCGCTGCA C HPCAL1 Ensembl:ENSG00000115756 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10302901..10303710 26863196 MeRIP-seq:(Medium) rs1443629401 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4622195,Human_RBP_ID_5146494,Human_RBP_ID_9330345,Human_RBP_ID_17135586,Human_RBP_ID_18193240,Human_RBP_ID_22997296,Human_RBP_ID_26818140 Human_Splice_Rec_217507,Human_Splice_Rec_217513 RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 77764 RMVar_ID_77764 Human_SNP_ID_60485667 m1A Human chr2 + 10312458 10312453 10312459 TCATCATCACTATCATCATTATCACCATCATCACCATCACCATCATCATTACTGTCATCATCACC TCATCATCACTATCATCATTATCACCAT______CATCACCATCATCATTACTGTCATCATCACC TCATCAC T HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10312455..10312882 26863196 MeRIP-seq:(Medium) rs1386044955 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_204697,Human_RBP_ID_2575609,Human_RBP_ID_26760288 RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 77765 RMVar_ID_77765 Human_SNP_ID_60496316 m1A Human chr2 + 10356288 10356286 10356288 ACGGGCCTATAGTGAATCATGAGTGCAGCATGAGAGTGTTAAAGGTCACAGGACGCCTCTTAGTG ACGGGCCTATAGTGAATCATGAGTGCAGCAT__GAGTGTTAAAGGTCACAGGACGCCTCTTAGTG TGA T HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10356285..10356410 26863196 MeRIP-seq:(Medium) rs748289636 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_104424,RMVar_hsa_circ_100523,RMVar_hsa_circ_196942,RMVar_hsa_circ_196943 77766 RMVar_ID_77766 Human_SNP_ID_60496318 m1A Human chr2 - 10356292 10356292 10356292 TTGGCACTAAGAGGCGTCCTGTGACCTTTAACACTCTCATGCTGCACTCATGATTCACTATAGGC TTGGCACTAAGAGGCGTCCTGTGACCTTTAACCCTCTCATGCTGCACTCATGATTCACTATAGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10356290..10356436 26863196 MeRIP-seq:(Medium) rs889561618 Functional Loss SNV dbSNP153 33..33 33 - - - 77767 RMVar_ID_77767 Human_SNP_ID_60496322 m1A Human chr2 - 10356315 10356315 10356315 AGGGGTCTCCACTATGAACTCCCTTGGCACTAAGAGGCGTCCTGTGACCTTTAACACTCTCATGC AGGGGTCTCCACTATGAACTCCCTTGGCACTAGGAGGCGTCCTGTGACCTTTAACACTCTCATGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10356309..10356405 26863196 MeRIP-seq:(Medium) rs965613188 Functional Loss SNV dbSNP153 33..33 33 - - - 77768 RMVar_ID_77768 Human_SNP_ID_60506388 m1A Human chr2 - 10396848 10396848 10396848 TCCAGGGAGTGTTTCCGCGTCCTGACTGGGCCACTAGACCATGCCCCTGGAAGAGAAGAGCGACA TCCAGGGAGTGTTTCCGCGTCCTGACTGGGCCCCTAGACCATGCCCCTGGAAGAGAAGAGCGACA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:10396826..10396875 26863196 MeRIP-seq:(Medium) rs984175690 Functional Loss SNV dbSNP153 33..33 33 - - - 77769 RMVar_ID_77769 Human_SNP_ID_60506401 m1A Human chr2 - 10396886 10396886 10396886 GAGACCAGGCGGAGGCTGAGAGGGAGTGGGTCAGAACCTCCAGGGAGTGTTTCCGCGTCCTGACT GAGACCAGGCGGAGGCTGAGAGGGAGTGGGTCTGAACCTCCAGGGAGTGTTTCCGCGTCCTGACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:10369204..10406316 26863196 MeRIP-seq:(Medium) rs896259466 Functional Loss SNV dbSNP153 33..33 33 - - - 77770 RMVar_ID_77770 Human_SNP_ID_60506402 m1A Human chr2 - 10396886 10396886 10396886 GAGACCAGGCGGAGGCTGAGAGGGAGTGGGTCAGAACCTCCAGGGAGTGTTTCCGCGTCCTGACT GAGACCAGGCGGAGGCTGAGAGGGAGTGGGTCCGAACCTCCAGGGAGTGTTTCCGCGTCCTGACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:10369204..10406316 26863196 MeRIP-seq:(Medium) rs896259466 Functional Loss SNV dbSNP153 33..33 33 - - - 77771 RMVar_ID_77771 Human_SNP_ID_60506403 m1A Human chr2 + 10396888 10396888 10396888 TCAGGACGCGGAAACACTCCCTGGAGGTTCTGACCCACTCCCTCTCAGCCTCCGCCTGGTCTCTG TCAGGACGCGGAAACACTCCCTGGAGGTTCTGGCCCACTCCCTCTCAGCCTCCGCCTGGTCTCTG A G HPCAL1 Ensembl:ENSG00000115756 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10396775..10406316 26863196 MeRIP-seq:(Medium) rs1013261324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_531185,Human_RBP_ID_4622198,Human_RBP_ID_9330346 Human_Splice_Rec_217508,Human_Splice_Rec_217509,Human_Splice_Rec_217514,Human_Splice_Rec_217515,Human_Splice_Rec_217522,Human_Splice_Rec_217523,Human_Splice_Rec_217534,Human_Splice_Rec_217535,Human_Splice_Rec_217546,Human_Splice_Rec_217547,Human_Splice_Rec_217554,Human_Splice_Rec_217555,Human_Splice_Rec_217562,Human_Splice_Rec_217563 Human_miRNA_ID_2712477,Human_miRNA_ID_2712478,Human_miRNA_ID_3048459,Human_miRNA_ID_3048460 RMVar_hsa_circ_104424,RMVar_hsa_circ_100523,RMVar_hsa_circ_196942,RMVar_hsa_circ_196947,RMVar_hsa_circ_337793,RMVar_hsa_circ_373737,RMVar_hsa_circ_196943,RMVar_hsa_circ_361674,RMVar_hsa_circ_298676,RMVar_hsa_circ_196945,RMVar_hsa_circ_196946,RMVar_hsa_circ_196944 77772 RMVar_ID_77772 Human_SNP_ID_60509561 m1A Human chr2 + 10407535 10407535 10407535 TTTGGGCCCTGTGGGGGTACAGTGGTGAACAAAAGGAGGCAGACAGTCAAGAGATTTTGTAAATA TTTGGGCCCTGTGGGGGTACAGTGGTGAACAACAGGAGGCAGACAGTCAAGAGATTTTGTAAATA A C HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10407532..10407732 26863196 MeRIP-seq:(Medium) rs1408425355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104424,RMVar_hsa_circ_100523,RMVar_hsa_circ_196942,RMVar_hsa_circ_373737,RMVar_hsa_circ_196943,RMVar_hsa_circ_361674,RMVar_hsa_circ_298676,RMVar_hsa_circ_196945,RMVar_hsa_circ_196946,RMVar_hsa_circ_196944 77773 RMVar_ID_77773 Human_SNP_ID_60509571 m1A Human chr2 - 10407562 10407562 10407562 CTCAGCATTTCCTGCCACCTGGCACTATATTTACAAAATCTCTTGACTGTCTGCCTCCTTTTGTT CTCAGCATTTCCTGCCACCTGGCACTATATTTGCAAAATCTCTTGACTGTCTGCCTCCTTTTGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10407560..10407696 26863196 MeRIP-seq:(Medium) rs1420380061 Functional Loss SNV dbSNP153 33..33 33 - - - 77774 RMVar_ID_77774 Human_SNP_ID_60513335 m1A Human chr2 - 10422987 10422986 10422987 GCATCTTCATCACAGACGACACCATCTTGTAGATGGCCTGCGGATGGGGGCAATGACACTGTGCT GCATCTTCATCACAGACGACACCATCTTGTAG_TGGCCTGCGGATGGGGGCAATGACACTGTGCT AT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:10422976..10423050 32194978 MeRIP-seq:(Medium) rs1469211580 Functional Loss DEL dbSNP153 33..33 33 - - - 77775 RMVar_ID_77775 Human_SNP_ID_60513362 m1A Human chr2 - 10423090 10423090 10423090 GTACACATGCAGCCCCGCCCCCACCCCGCACTACCGTCATTGTTGGTGTCCATCTGCCTGAAGAT GTACACATGCAGCCCCGCCCCCACCCCGCACTGCCGTCATTGTTGGTGTCCATCTGCCTGAAGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10423054..10423126 26863196 MeRIP-seq:(Medium) rs112732178 Functional Loss SNV dbSNP153 33..33 33 - - - 77776 RMVar_ID_77776 Human_SNP_ID_60516351 m1A Human chr2 - 10433375 10433375 10433375 CACCACCACACACGCAAACATACCACACACATACACATCGCACACACGGTCACACCATGCCCACA CACCACCACACACGCAAACATACCACACACATCCACATCGCACACACGGTCACACCATGCCCACA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10433311..10433412 26863196 MeRIP-seq:(Medium) rs1201687088 Functional Loss SNV dbSNP153 33..33 33 - - - 77777 RMVar_ID_77777 Human_SNP_ID_60516400 m1A Human chr2 - 10433492 10433489 10433493 GCAAACATACCACACACATCCACAGCACACACACAGTCACACCATCCCTCACACACCACTACACA GCAAACATACCACACACATCCACAGCACACA____GTCACACCATCCCTCACACACCACTACACA CTGTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10433329..10433525 26863196 MeRIP-seq:(Medium) rs372434427 Functional Loss DEL dbSNP153 32..35 33 - - - 77778 RMVar_ID_77778 Human_SNP_ID_60516401 m1A Human chr2 - 10433492 10433489 10433493 GCAAACATACCACACACATCCACAGCACACACACAGTCACACCATCCCTCACACACCACTACACA GCAAACATACCACACACATCCACAGCACACA__CAGTCACACCATCCCTCACACACCACTACACA CTGTG CTG - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:10433329..10433525 26863196 MeRIP-seq:(Medium) rs372434427 Functional Loss DEL dbSNP153 32..33 33 - - - 77779 RMVar_ID_77779 Human_SNP_ID_60518448 m1A Human chr2 - 10440710 10440710 10440710 GGCTAGTATTAATGTGTAGATAGCACTCTGGTAGCTGTTAACTGCAAGTTTAGCTTGAATTAAGG GGCTAGTATTAATGTGTAGATAGCACTCTGGTGGCTGTTAACTGCAAGTTTAGCTTGAATTAAGG T C ODC1 Ensembl:ENSG00000115758 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:10440560..10440710 32194978 MeRIP-seq:(Medium) rs749410471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_531286,Human_RBP_ID_1576467,Human_RBP_ID_1894841,Human_RBP_ID_2576251,Human_RBP_ID_4576658,Human_RBP_ID_5146506,Human_RBP_ID_6810536,Human_RBP_ID_8841001,Human_RBP_ID_9092004,Human_RBP_ID_9294685,Human_RBP_ID_13565916,Human_RBP_ID_17388462,Human_RBP_ID_18308672,Human_RBP_ID_21894073,Human_RBP_ID_23816452,Human_RBP_ID_26487834 RMVar_hsa_circ_120427,RMVar_hsa_circ_127518,RMVar_hsa_circ_123923,RMVar_hsa_circ_196951,RMVar_hsa_circ_196952,RMVar_hsa_circ_196953 77780 RMVar_ID_77780 Human_SNP_ID_60558743 m1A Human chr2 - 10589146 10589143 10589146 AGGAGGAAAAAGTGAAGCGGCAGGAACGACTCAAGGAGGACCAGCAGACAGTCCTAAAGCCCCAG AGGAGGAAAAAGTGAAGCGGCAGGAACGACTC___GAGGACCAGCAGACAGTCCTAAAGCCCCAG CCTT C NOL10 Ensembl:ENSG00000115761 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:10572155..10589639 32194978 MeRIP-seq:(Medium) rs748751301 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_26338957 RMVar_hsa_circ_57165,RMVar_hsa_circ_341133,RMVar_hsa_circ_196965,RMVar_hsa_circ_196964,RMVar_hsa_circ_327911,RMVar_hsa_circ_365004,RMVar_hsa_circ_348261,RMVar_hsa_circ_284608,RMVar_hsa_circ_338290,RMVar_hsa_circ_61610,RMVar_hsa_circ_196966,RMVar_hsa_circ_196967 77781 RMVar_ID_77781 Human_SNP_ID_60558745 m1A Human chr2 - 10589146 10589146 10589146 AGGAGGAAAAAGTGAAGCGGCAGGAACGACTCAAGGAGGACCAGCAGACAGTCCTAAAGCCCCAG AGGAGGAAAAAGTGAAGCGGCAGGAACGACTCGAGGAGGACCAGCAGACAGTCCTAAAGCCCCAG T C NOL10 Ensembl:ENSG00000115761 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:10572155..10589639 32194978 MeRIP-seq:(Medium) rs1245803260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26338957 RMVar_hsa_circ_57165,RMVar_hsa_circ_341133,RMVar_hsa_circ_196965,RMVar_hsa_circ_196964,RMVar_hsa_circ_327911,RMVar_hsa_circ_365004,RMVar_hsa_circ_348261,RMVar_hsa_circ_284608,RMVar_hsa_circ_338290,RMVar_hsa_circ_61610,RMVar_hsa_circ_196966,RMVar_hsa_circ_196967 77782 RMVar_ID_77782 Human_SNP_ID_60567308 m1A Human chr2 - 10622951 10622951 10622951 GGTGATTCGTGGGGGAGTGATGGATGATGGGGAGAGAGGGGAACTGAATGAGCAGTGGTACCATT GGTGATTCGTGGGGGAGTGATGGATGATGGGGGGAGAGGGGAACTGAATGAGCAGTGGTACCATT T C NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10622948..10623064 26863196 MeRIP-seq:(Medium) rs933203966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47263,RMVar_hsa_circ_196964,RMVar_hsa_circ_348261,RMVar_hsa_circ_61610,RMVar_hsa_circ_196969,RMVar_hsa_circ_324439,RMVar_hsa_circ_67183,RMVar_hsa_circ_295736,RMVar_hsa_circ_51498,RMVar_hsa_circ_1773,RMVar_hsa_circ_196968,RMVar_hsa_circ_362737,RMVar_hsa_circ_94451,RMVar_hsa_circ_374574,RMVar_hsa_circ_196975,RMVar_hsa_circ_196972,RMVar_hsa_circ_196973,RMVar_hsa_circ_196977,RMVar_hsa_circ_196974,RMVar_hsa_circ_196976 77783 RMVar_ID_77783 Human_SNP_ID_60575163 m1A Human chr2 + 10652705 10652705 10652705 CTCCCAAATGAACCAGCTCCTGCTCACTTCTTATCTCACTCCCAGCTTTCCCTATCAGTAATCTC CTCCCAAATGAACCAGCTCCTGCTCACTTCTTCTCTCACTCCCAGCTTTCCCTATCAGTAATCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10652654..10652742 26863196 MeRIP-seq:(Medium) rs1378997318 Functional Loss SNV dbSNP153 33..33 33 - - - 77784 RMVar_ID_77784 Human_SNP_ID_60585089 m1A Human chr2 - 10689735 10689735 10689735 CGAGCTCTTGGGGGTCGTCCTCCTCGTGGGGCAGCCGCCCCTCTCCTCGGCCCTAGCCTCTGTTT CGAGCTCTTGGGGGTCGTCCTCCTCGTGGGGCGGCCGCCCCTCTCCTCGGCCCTAGCCTCTGTTT T C NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:10689731..10689838 32194978 MeRIP-seq:(Medium) rs374452760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22360823 77785 RMVar_ID_77785 Human_SNP_ID_60585185 m1A Human chr2 - 10689892 10689892 10689892 ATTACGGTGCTCGAGCACGCTGGTGGGAAAGGACCCGGGACTTGAACAGTGTTGTGCGGCGCCAT ATTACGGTGCTCGAGCACGCTGGTGGGAAAGGTCCCGGGACTTGAACAGTGTTGTGCGGCGCCAT T A NOL10 Ensembl:ENSG00000115761 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10689841..10689957 26863196 MeRIP-seq:(Medium) rs772127698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623109,Human_RBP_ID_13570804,Human_RBP_ID_18421689,Human_RBP_ID_18743894,Human_RBP_ID_22997123,Human_RBP_ID_23817110 Human_Splice_Rec_217657,Human_Splice_Rec_217697,Human_Splice_Rec_217735,Human_Splice_Rec_217789 77786 RMVar_ID_77786 Human_SNP_ID_60585192 m1A Human chr2 + 10689901 10689901 10689901 CACAACACTGTTCAAGTCCCGGGTCCTTTCCCACCAGCGTGCTCGAGCACCGTAATCCCGGGACC CACAACACTGTTCAAGTCCCGGGTCCTTTCCCCCCAGCGTGCTCGAGCACCGTAATCCCGGGACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10689851..10689946 26863196 MeRIP-seq:(Medium) rs1412181098 Functional Loss SNV dbSNP153 33..33 33 - - - 77787 RMVar_ID_77787 Human_SNP_ID_60585297 m1A Human chr2 - 10690093 10690093 10690093 TAGTCTTGCCCGTAGCAGCGTCGCCGACAGCCACGCCGGGTTGTCAGAGCCTCACTAGTTTTTCT TAGTCTTGCCCGTAGCAGCGTCGCCGACAGCCGCGCCGGGTTGTCAGAGCCTCACTAGTTTTTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10690049..10690120 26863196 MeRIP-seq:(Medium) rs186353990 Functional Loss SNV dbSNP153 33..33 33 - - - 77788 RMVar_ID_77788 Human_SNP_ID_60593767 m1A Human chr2 + 10721674 10721674 10721674 TCCCGGGAGCCGGCAGAGCGCTCCGGCCCCGCACCCGCCGCCCGTCGCCCGCAGCCCCCTACCGC TCCCGGGAGCCGGCAGAGCGCTCCGGCCCCGCCCCCGCCGCCCGTCGCCCGCAGCCCCCTACCGC A C ATP6V1C2 Ensembl:ENSG00000143882 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:10721639..10721724 26863410 MeRIP-seq:(Medium) rs969380472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_217831,Human_Splice_Rec_217857 77789 RMVar_ID_77789 Human_SNP_ID_60611496 m1A Human chr2 + 10787307 10787307 10787307 AATTACCTGAGAAACTCGTTGATGCCTTGCTCACTGAAGGAGCCTTTTAGCAGAGCAAATTTCAT AATTACCTGAGAAACTCGTTGATGCCTTGCTCGCTGAAGGAGCCTTTTAGCAGAGCAAATTTCAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:10787276..10787325 26863196 MeRIP-seq:(Medium) rs779840295 Functional Loss SNV dbSNP153 33..33 33 - - - 77790 RMVar_ID_77790 Human_SNP_ID_60611514 m1A Human chr2 + 10787349 10787349 10787349 CCTTTTAGCAGAGCAAATTTCATCTTGCGTGCATTGATGGCGGCCATGGCGGGGTACCCAAACCC CCTTTTAGCAGAGCAAATTTCATCTTGCGTGCGTTGATGGCGGCCATGGCGGGGTACCCAAACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:10787234..10787428 26863196 MeRIP-seq:(Medium) rs771527973 Functional Loss SNV dbSNP153 33..33 33 - - - 77791 RMVar_ID_77791 Human_SNP_ID_60611515 m1A Human chr2 - 10787350 10787350 10787350 AGGGTTTGGGTACCCCGCCATGGCCGCCATCAATGCACGCAAGATGAAATTTGCTCTGCTAAAAG AGGGTTTGGGTACCCCGCCATGGCCGCCATCAGTGCACGCAAGATGAAATTTGCTCTGCTAAAAG T C PDIA6 Ensembl:ENSG00000143870 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:10787299..10787472 26863196 MeRIP-seq:(Medium) rs774736094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242901,Human_RBP_ID_922727,Human_RBP_ID_1374924,Human_RBP_ID_4577158,Human_RBP_ID_9092141,Human_RBP_ID_9353774,Human_RBP_ID_17937667,Human_RBP_ID_22450131,Human_RBP_ID_22504258,Human_RBP_ID_22764874,Human_RBP_ID_22997759,Human_RBP_ID_23817418,Human_RBP_ID_26999178 Human_Splice_Rec_217934,Human_Splice_Rec_217935,Human_Splice_Rec_217960,Human_Splice_Rec_217961,Human_Splice_Rec_217986,Human_Splice_Rec_217987,Human_Splice_Rec_218014,Human_Splice_Rec_218015,Human_Splice_Rec_218040,Human_Splice_Rec_218041,Human_Splice_Rec_218066,Human_Splice_Rec_218067 Human_miRNA_ID_2444860,Human_miRNA_ID_2446243 RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303,RMVar_hsa_circ_196996,RMVar_hsa_circ_314125,RMVar_hsa_circ_336161,RMVar_hsa_circ_379037,RMVar_hsa_circ_340509,RMVar_hsa_circ_330605,RMVar_hsa_circ_290480 77792 RMVar_ID_77792 Human_SNP_ID_60611525 m1A Human chr2 + 10787393 10787393 10787393 CATGGCGGGGTACCCAAACCCTCCAATCCCCAACGCGGTCTCAAGTTCAGACTGGGCTCCAGCTT CATGGCGGGGTACCCAAACCCTCCAATCCCCAGCGCGGTCTCAAGTTCAGACTGGGCTCCAGCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:10787242..10787394;chr2:10787347..10787479 26863196 MeRIP-seq:(Medium) rs754006477 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 77793 RMVar_ID_77793 Human_SNP_ID_60611526 m1A Human chr2 + 10787393 10787393 10787393 CATGGCGGGGTACCCAAACCCTCCAATCCCCAACGCGGTCTCAAGTTCAGACTGGGCTCCAGCTT CATGGCGGGGTACCCAAACCCTCCAATCCCCATCGCGGTCTCAAGTTCAGACTGGGCTCCAGCTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:10787242..10787394;chr2:10787347..10787479 26863196 MeRIP-seq:(Medium) rs754006477 Functional Loss SNV dbSNP153 33..33 33 - - - 77794 RMVar_ID_77794 Human_SNP_ID_60612259 m1A Human chr2 - 10789777 10789777 10789777 CATCGTGTCCCGGGCCCTTGATTTGTTTTCTGATAACGCCCCACCTCCTGAGCTGCTTGAGGTAA CATCGTGTCCCGGGCCCTTGATTTGTTTTCTGGTAACGCCCCACCTCCTGAGCTGCTTGAGGTAA T C PDIA6 Ensembl:ENSG00000143870 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs150300054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_531643,Human_RBP_ID_922731,Human_RBP_ID_1576656,Human_RBP_ID_3591542,Human_RBP_ID_4577176,Human_RBP_ID_6812154,Human_RBP_ID_9259619,Human_RBP_ID_13572773,Human_RBP_ID_18743995,Human_RBP_ID_19099288,Human_RBP_ID_22450138,Human_RBP_ID_22764882,Human_RBP_ID_25452815,Human_RBP_ID_26338454 Human_Splice_Rec_217929,Human_Splice_Rec_217955,Human_Splice_Rec_217981,Human_Splice_Rec_218009,Human_Splice_Rec_218035,Human_Splice_Rec_218061 Human_miRNA_ID_2211299,Human_miRNA_ID_2470449,Human_miRNA_ID_2524415 RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303,RMVar_hsa_circ_196997,RMVar_hsa_circ_196996,RMVar_hsa_circ_314125,RMVar_hsa_circ_336161,RMVar_hsa_circ_379037,RMVar_hsa_circ_340509,RMVar_hsa_circ_290480,RMVar_hsa_circ_196999,RMVar_hsa_circ_302789,RMVar_hsa_circ_315097,RMVar_hsa_circ_297066,RMVar_hsa_circ_196998 77795 RMVar_ID_77795 Human_SNP_ID_60618470 m1A Human chr2 - 10812664 10812664 10812664 ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCAGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCGGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:10812662..10812775 26863410 MeRIP-seq:(Medium) rs6726687 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19103455,Human_RBP_ID_22359867,Human_RBP_ID_26786765 GWAS_ID_9300,GWAS_ID_9301,GWAS_ID_9302,GWAS_ID_9303,GWAS_ID_9304,GWAS_ID_9305,GWAS_ID_9306,GWAS_ID_9307 77796 RMVar_ID_77796 Human_SNP_ID_60618495 m1A Human chr2 - 10812696 10812696 10812696 CGGTGGGGACTGCACGTAGCCCGGCGCTCGGCATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCA CGGTGGGGACTGCACGTAGCCCGGCGCTCGGCGTGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCA T C PDIA6 Ensembl:ENSG00000143870 Protein coding start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr2:10812681..10812770;chr2:10812677..10812766 26863410 MeRIP-seq:(Medium) rs1368552415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243735,Human_RBP_ID_531897,Human_RBP_ID_4577481,Human_RBP_ID_5322413,Human_RBP_ID_6967515,Human_RBP_ID_8498760,Human_RBP_ID_8841265,Human_RBP_ID_9330353,Human_RBP_ID_13575829,Human_RBP_ID_18744129,Human_RBP_ID_22449715,Human_RBP_ID_23817759,Human_RBP_ID_26999484 Human_Splice_Rec_217915,Human_Splice_Rec_217939,Human_Splice_Rec_218071 77797 RMVar_ID_77797 Human_SNP_ID_60618499 m1A Human chr2 + 10812725 10812702 10812726 CCATGCCGAGCGCCGGGCTACGTGCAGTCCCCACCGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC CCATGCCGAG________________________CGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC GCGCCGGGCTACGTGCAGTCCCCAC G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:10812701..10812775 26863196 MeRIP-seq:(Medium) rs1202045787 Functional Loss DEL dbSNP153 11..34 33 - - - 77798 RMVar_ID_77798 Human_SNP_ID_60618514 m1A Human chr2 + 10812718 10812718 10812718 AGGAGAGCCATGCCGAGCGCCGGGCTACGTGCAGTCCCCACCGCCGCCGCCGCTTCAGCCCTGCA AGGAGAGCCATGCCGAGCGCCGGGCTACGTGCTGTCCCCACCGCCGCCGCCGCTTCAGCCCTGCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:10812701..10812775 32194978 MeRIP-seq:(Medium) rs984970812 Functional Loss SNV dbSNP153 33..33 33 - - - 77799 RMVar_ID_77799 Human_SNP_ID_60618522 m1A Human chr2 + 10812725 10812725 10812725 CCATGCCGAGCGCCGGGCTACGTGCAGTCCCCACCGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC CCATGCCGAGCGCCGGGCTACGTGCAGTCCCCGCCGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:10812701..10812775 26863196 MeRIP-seq:(Medium) rs13010424 Functional Loss SNV dbSNP153 33..33 33 - - - 77800 RMVar_ID_77800 Human_SNP_ID_60618523 m1A Human chr2 + 10812725 10812725 10812725 CCATGCCGAGCGCCGGGCTACGTGCAGTCCCCACCGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC CCATGCCGAGCGCCGGGCTACGTGCAGTCCCCTCCGCCGCCGCCGCTTCAGCCCTGCAGCGTGCC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:10812701..10812775 26863196 MeRIP-seq:(Medium) rs13010424 Functional Loss SNV dbSNP153 33..33 33 - - - 77801 RMVar_ID_77801 Human_SNP_ID_60707793 m1A Human chr2 - 11155514 11155514 11155514 AGCGCCACGGGCGCGGGCACCTGGGCGGCCGCAGCGAGAAGGGACCGCTCAGCCTCGGCGGCGCA AGCGCCACGGGCGCGGGCACCTGGGCGGCCGCGGCGAGAAGGGACCGCTCAGCCTCGGCGGCGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:11155464..11155649 26863196 MeRIP-seq:(Medium) rs767021061 Functional Loss SNV dbSNP153 33..33 33 - - - 77802 RMVar_ID_77802 Human_SNP_ID_60722405 m1A Human chr2 - 11211631 11211631 11211631 AGGGTTTTCCAGCAGCGTCTTCCTAAGAATTGATTCTGTGTTAGCTTTTTGGTTTTGAAACATTT AGGGTTTTCCAGCAGCGTCTTCCTAAGAATTGGTTCTGTGTTAGCTTTTTGGTTTTGAAACATTT T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:11211630..11211748 32194978 MeRIP-seq:(Medium) rs1377475107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52352,RMVar_hsa_circ_115102,RMVar_hsa_circ_128041,RMVar_hsa_circ_117959,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_77214,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197014,RMVar_hsa_circ_197015,RMVar_hsa_circ_197012,RMVar_hsa_circ_197013,RMVar_hsa_circ_197011,RMVar_hsa_circ_197006,RMVar_hsa_circ_197008,RMVar_hsa_circ_197009,RMVar_hsa_circ_197007,RMVar_hsa_circ_73035,RMVar_hsa_circ_44462,RMVar_hsa_circ_197026,RMVar_hsa_circ_94695,RMVar_hsa_circ_117132,RMVar_hsa_circ_66754,RMVar_hsa_circ_197031,RMVar_hsa_circ_358841,RMVar_hsa_circ_197032,RMVar_hsa_circ_305010,RMVar_hsa_circ_64319,RMVar_hsa_circ_61039,RMVar_hsa_circ_62445,RMVar_hsa_circ_44496,RMVar_hsa_circ_12182,RMVar_hsa_circ_13441,RMVar_hsa_circ_43502,RMVar_hsa_circ_197034,RMVar_hsa_circ_57851,RMVar_hsa_circ_307909,RMVar_hsa_circ_334957,RMVar_hsa_circ_35679,RMVar_hsa_circ_13818,RMVar_hsa_circ_197036,RMVar_hsa_circ_197037,RMVar_hsa_circ_73093 77803 RMVar_ID_77803 Human_SNP_ID_60740883 m1A Human chr2 - 11287726 11287726 11287726 TCCTCTTTTTATTTCTTAACAGGATGGCTTAAATTCCTTGGTCCTTGATTTAGATTTTCCTGCTT TCCTCTTTTTATTTCTTAACAGGATGGCTTAAGTTCCTTGGTCCTTGATTTAGATTTTCCTGCTT T C ROCK2 Ensembl:ENSG00000134318 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:11287676..11287750 26863196 MeRIP-seq:(Medium) rs1558361922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_218226,Human_Splice_Rec_218227,Human_Splice_Rec_218290,Human_Splice_Rec_218291,Human_Splice_Rec_218414,Human_Splice_Rec_218415,Human_Splice_Rec_218445,Human_Splice_Rec_218458,Human_Splice_Rec_218459 RMVar_hsa_circ_113994,RMVar_hsa_circ_197006,RMVar_hsa_circ_94695,RMVar_hsa_circ_197031,RMVar_hsa_circ_6528,RMVar_hsa_circ_111154,RMVar_hsa_circ_197045,RMVar_hsa_circ_197046,RMVar_hsa_circ_357373,RMVar_hsa_circ_311577,RMVar_hsa_circ_197047,RMVar_hsa_circ_197048 77804 RMVar_ID_77804 Human_SNP_ID_60755136 m1A Human chr2 - 11343975 11343975 11343975 GAGAGCTTGCTGGTAGGTGGCCGGGGCCTGGGAGCTTGCTCGTTGCAGCTCACACCTCAGATCCC GAGAGCTTGCTGGTAGGTGGCCGGGGCCTGGGGGCTTGCTCGTTGCAGCTCACACCTCAGATCCC T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:11343969..11344120 32194978 MeRIP-seq:(Medium) rs1224579732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19001154,Human_RBP_ID_19096894,Human_RBP_ID_26786768 RMVar_hsa_circ_113994,RMVar_hsa_circ_197006 77805 RMVar_ID_77805 Human_SNP_ID_60755386 m1A Human chr2 - 11344560 11344549 11344560 GGGACTGCAAGGCGGCCGGCGGCGACCATGGCAGCGGGCCGGCGGCGGCCGTAGTGGCCCAGGCC GGGACTGCAAGGCGGCCGGCGGCGACCATGGC___________GGCGGCCGTAGTGGCCCAGGCC CGCCGGCCCGCT C ROCK2 Ensembl:ENSG00000134318 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:11344511..11344628 26863196 MeRIP-seq:(Medium) rs1165821958 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_4622217,Human_RBP_ID_18421691,Human_RBP_ID_18470965,Human_RBP_ID_22450148 RMVar_hsa_circ_113994,RMVar_hsa_circ_197006 77806 RMVar_ID_77806 Human_SNP_ID_60755389 m1A Human chr2 - 11344560 11344560 11344560 GGGACTGCAAGGCGGCCGGCGGCGACCATGGCAGCGGGCCGGCGGCGGCCGTAGTGGCCCAGGCC GGGACTGCAAGGCGGCCGGCGGCGACCATGGCGGCGGGCCGGCGGCGGCCGTAGTGGCCCAGGCC T C ROCK2 Ensembl:ENSG00000134318 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:11344511..11344628 26863196 MeRIP-seq:(Medium) rs1211972817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622217,Human_RBP_ID_18421691,Human_RBP_ID_18470965,Human_RBP_ID_22450148 RMVar_hsa_circ_113994,RMVar_hsa_circ_197006 77807 RMVar_ID_77807 Human_SNP_ID_60763515 m1A Human chr2 + 11374593 11374593 11374593 GCCCTCGCCCCTGGGGCCCTGTGAGAGCCAGGACAGGCCCTCCCCTCATCCAGCGGCCGTGGAGC GCCCTCGCCCCTGGGGCCCTGTGAGAGCCAGGGCAGGCCCTCCCCTCATCCAGCGGCCGTGGAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:11374570..11374674 26863196 MeRIP-seq:(Medium) rs752587654 Functional Loss SNV dbSNP153 33..33 33 - - - 77808 RMVar_ID_77808 Human_SNP_ID_60770889 m1A Human chr2 - 11402350 11402350 11402350 CTTCTTCTCTCCTCCCTCTTGACTCTTTTCCCACCCGCCTCCTGCCATTGACTCCAGCCTATAGA CTTCTTCTCTCCTCCCTCTTGACTCTTTTCCCCCCCGCCTCCTGCCATTGACTCCAGCCTATAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:11402302..11402464 26863196 MeRIP-seq:(Medium) rs1015616216 Functional Loss SNV dbSNP153 33..33 33 - - - 77809 RMVar_ID_77809 Human_SNP_ID_60788475 m1A Human chr2 + 11472078 11472078 11472078 AAAGTGTGAGGACAGATGCAGGTTAATTTGTAAGGTACTTTGGCAGGAAGTTGAGGGAATTCTTA AAAGTGTGAGGACAGATGCAGGTTAATTTGTAGGGTACTTTGGCAGGAAGTTGAGGGAATTCTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:11472044..11472122 26863196 MeRIP-seq:(Medium) rs1010271735 Functional Loss SNV dbSNP153 33..33 33 - - - 77810 RMVar_ID_77810 Human_SNP_ID_60859816 m1A Human chr2 - 11753020 11753019 11753020 TGTAGAACTCCAGCACACAGCAGACGCTCCAAAGCATTCACGACCGCAATTTCATACAGTTCCAG TGTAGAACTCCAGCACACAGCAGACGCTCCAA_GCATTCACGACCGCAATTTCATACAGTTCCAG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:11753011..11753082 26863196 MeRIP-seq:(Medium) rs1394918084 Functional Loss DEL dbSNP153 33..33 33 - - - 77811 RMVar_ID_77811 Human_SNP_ID_60875716 m1A Human chr2 + 11812888 11812888 11812888 AGCAACGGAGGCCAGGAGGCCATGCGGTGTGGACGTGGTGGGAGCACTGGGTGGTGCCGAGGGTG AGCAACGGAGGCCAGGAGGCCATGCGGTGTGGTCGTGGTGGGAGCACTGGGTGGTGCCGAGGGTG A T LPIN1 Ensembl:ENSG00000134324 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:11812838..11813024 26863196 MeRIP-seq:(Medium) rs775079802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25367,RMVar_hsa_circ_15893,RMVar_hsa_circ_265565,RMVar_hsa_circ_197085,RMVar_hsa_circ_52148,RMVar_hsa_circ_364153,RMVar_hsa_circ_369469,RMVar_hsa_circ_197086 77812 RMVar_ID_77812 Human_SNP_ID_60876049 m1A Human chr2 + 11814136 11814136 11814136 TTTGAGGCTGGCAGAGCTGATGGGAGCAGGCGAGCTGCTGTGTCTGGGAAGCGGTGGCTGCTGAG TTTGAGGCTGGCAGAGCTGATGGGAGCAGGCGGGCTGCTGTGTCTGGGAAGCGGTGGCTGCTGAG A G LPIN1 Ensembl:ENSG00000134324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:11814074..11814174 26863196 MeRIP-seq:(Medium) rs1318164392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25367,RMVar_hsa_circ_15893,RMVar_hsa_circ_265565,RMVar_hsa_circ_197085,RMVar_hsa_circ_52148,RMVar_hsa_circ_364153,RMVar_hsa_circ_369469,RMVar_hsa_circ_197086 77813 RMVar_ID_77813 Human_SNP_ID_205532300 m1A Human chr4 - 138203953 138203953 138203953 TAGTATGTAGACTGTTTTGACTAAAGGAAAGGATTGTGAAGAGGAGTCAAAATCAAGATAGTAGT TAGTATGTAGACTGTTTTGACTAAAGGAAAGGTTTGTGAAGAGGAGTCAAAATCAAGATAGTAGT T A SLC7A11 Ensembl:ENSG00000151012 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:138203904..138204004 26863196 MeRIP-seq:(Medium) rs921733700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89824,RMVar_hsa_circ_228648,RMVar_hsa_circ_3146,RMVar_hsa_circ_228655,RMVar_hsa_circ_46501,RMVar_hsa_circ_115301,RMVar_hsa_circ_228656,RMVar_hsa_circ_370756 77814 RMVar_ID_77814 Human_SNP_ID_205532301 m1A Human chr4 - 138203953 138203953 138203953 TAGTATGTAGACTGTTTTGACTAAAGGAAAGGATTGTGAAGAGGAGTCAAAATCAAGATAGTAGT TAGTATGTAGACTGTTTTGACTAAAGGAAAGGGTTGTGAAGAGGAGTCAAAATCAAGATAGTAGT T C SLC7A11 Ensembl:ENSG00000151012 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:138203904..138204004 26863196 MeRIP-seq:(Medium) rs921733700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89824,RMVar_hsa_circ_228648,RMVar_hsa_circ_3146,RMVar_hsa_circ_228655,RMVar_hsa_circ_46501,RMVar_hsa_circ_115301,RMVar_hsa_circ_228656,RMVar_hsa_circ_370756 77815 RMVar_ID_77815 Human_SNP_ID_205541240 m1A Human chr4 - 138241937 138241937 138241937 GGCAGGAGAAAGTGCAGCTGAAGAGGAAAGTCACTTTACTGAGGGGAGTCTCCATTATCATTGGC GGCAGGAGAAAGTGCAGCTGAAGAGGAAAGTCCCTTTACTGAGGGGAGTCTCCATTATCATTGGC T G SLC7A11 Ensembl:ENSG00000151012 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:138241774..138242012 26863196 MeRIP-seq:(Medium) rs931682205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607257,Human_RBP_ID_22095679,Human_RBP_ID_23034732 Human_miRNA_ID_65676,Human_miRNA_ID_564953,Human_miRNA_ID_1727881,Human_miRNA_ID_2376062,Human_miRNA_ID_2884450,Human_miRNA_ID_3031707 RMVar_hsa_circ_379113,RMVar_hsa_circ_228660,RMVar_hsa_circ_228661 77816 RMVar_ID_77816 Human_SNP_ID_205713816 m1A Human chr4 - 138975722 138975721 138975722 GTGAGACACCTTGGGGCGGGCGGGGGTGAGGTAGGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC GTGAGACACCTTGGGGCGGGCGGGGGTGAGGT_GGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC CT C AC109927.1 Ensembl:ENSG00000250195 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:138975676..138975750 26863196 MeRIP-seq:(Medium) rs1327693103 Functional Loss DEL dbSNP153 33..33 33 - - - 77817 RMVar_ID_77817 Human_SNP_ID_205713819 m1A Human chr4 - 138975722 138975721 138975723 GTGAGACACCTTGGGGCGGGCGGGGGTGAGGTAGGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC GTGAGACACCTTGGGGCGGGCGGGGGTGAGG__GGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC CTA C AC109927.1 Ensembl:ENSG00000250195 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:138975676..138975750 26863196 MeRIP-seq:(Medium) rs1560716559 Functional Loss DEL dbSNP153 32..33 33 - - - 77818 RMVar_ID_77818 Human_SNP_ID_205713820 m1A Human chr4 - 138975722 138975722 138975722 GTGAGACACCTTGGGGCGGGCGGGGGTGAGGTAGGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC GTGAGACACCTTGGGGCGGGCGGGGGTGAGGTGGGGGCGGGGGGGGGGGCGCTGGGCGTGGCTTC T C AC109927.1 Ensembl:ENSG00000250195 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:138975676..138975750 26863196 MeRIP-seq:(Medium) rs1299333121 Functional Loss SNV dbSNP153 33..33 33 - - - 77819 RMVar_ID_77819 Human_SNP_ID_205723708 m1A Human chr4 - 139015801 139015801 139015801 CCGGGCAGCAGAGCCGGAGAGGGAGGTGCAACACCGCTGCGTCGGCACCGTCTGCTGTGAGACCT CCGGGCAGCAGAGCCGGAGAGGGAGGTGCAACGCCGCTGCGTCGGCACCGTCTGCTGTGAGACCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:139015795..139015950 26863196 MeRIP-seq:(Medium) rs987787634 Functional Loss SNV dbSNP153 33..33 33 - - - 77820 RMVar_ID_77820 Human_SNP_ID_205741575 m1A Human chr4 + 139083780 139083780 139083780 AGACAACAGCCTCACTCACTTCCTGGTTCCTCAGCAACTGGGGTGAAGCGCACAACTCGTCCGCC AGACAACAGCCTCACTCACTTCCTGGTTCCTCGGCAACTGGGGTGAAGCGCACAACTCGTCCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139083776..139084023 26863196 MeRIP-seq:(Medium) rs1043676224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24036580 77821 RMVar_ID_77821 Human_SNP_ID_205741752 m1A Human chr4 - 139084211 139084211 139084211 GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCAGCTCCAGCCCCGGGATAAACATGGCGACGTCT GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCTGCTCCAGCCCCGGGATAAACATGGCGACGTCT T A ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139084198..139084389 26863196 MeRIP-seq:(Medium) rs768430541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_609323,Human_Splice_Rec_609335,Human_Splice_Rec_609345,Human_Splice_Rec_609357,Human_Splice_Rec_609375 RMVar_hsa_circ_228676,RMVar_hsa_circ_12262,RMVar_hsa_circ_96628,RMVar_hsa_circ_228670,RMVar_hsa_circ_228667,RMVar_hsa_circ_228669,RMVar_hsa_circ_365851,RMVar_hsa_circ_228674,RMVar_hsa_circ_288745,RMVar_hsa_circ_366492,RMVar_hsa_circ_81011,RMVar_hsa_circ_47514,RMVar_hsa_circ_269030,RMVar_hsa_circ_318390,RMVar_hsa_circ_228680,RMVar_hsa_circ_228681 77822 RMVar_ID_77822 Human_SNP_ID_205741753 m1A Human chr4 - 139084211 139084211 139084211 GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCAGCTCCAGCCCCGGGATAAACATGGCGACGTCT GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCGGCTCCAGCCCCGGGATAAACATGGCGACGTCT T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139084198..139084389 26863196 MeRIP-seq:(Medium) rs768430541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_609323,Human_Splice_Rec_609335,Human_Splice_Rec_609345,Human_Splice_Rec_609357,Human_Splice_Rec_609375 RMVar_hsa_circ_228676,RMVar_hsa_circ_12262,RMVar_hsa_circ_96628,RMVar_hsa_circ_228670,RMVar_hsa_circ_228667,RMVar_hsa_circ_228669,RMVar_hsa_circ_365851,RMVar_hsa_circ_228674,RMVar_hsa_circ_288745,RMVar_hsa_circ_366492,RMVar_hsa_circ_81011,RMVar_hsa_circ_47514,RMVar_hsa_circ_269030,RMVar_hsa_circ_318390,RMVar_hsa_circ_228680,RMVar_hsa_circ_228681 77823 RMVar_ID_77823 Human_SNP_ID_205741754 m1A Human chr4 - 139084211 139084211 139084211 GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCAGCTCCAGCCCCGGGATAAACATGGCGACGTCT GCTGCTCACGGTGTAAGTCAATGTGAAGCAGCCGCTCCAGCCCCGGGATAAACATGGCGACGTCT T G ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139084198..139084389 26863196 MeRIP-seq:(Medium) rs768430541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_609323,Human_Splice_Rec_609335,Human_Splice_Rec_609345,Human_Splice_Rec_609357,Human_Splice_Rec_609375 RMVar_hsa_circ_228676,RMVar_hsa_circ_12262,RMVar_hsa_circ_96628,RMVar_hsa_circ_228670,RMVar_hsa_circ_228667,RMVar_hsa_circ_228669,RMVar_hsa_circ_365851,RMVar_hsa_circ_228674,RMVar_hsa_circ_288745,RMVar_hsa_circ_366492,RMVar_hsa_circ_81011,RMVar_hsa_circ_47514,RMVar_hsa_circ_269030,RMVar_hsa_circ_318390,RMVar_hsa_circ_228680,RMVar_hsa_circ_228681 77824 RMVar_ID_77824 Human_SNP_ID_205741772 m1A Human chr4 + 139084255 139084251 139084255 TTGACTTACACCGTGAGCAGCGGCGGCAGGGGAGGAGGCGGAACCCGCGGCCGGAGACACACGCC TTGACTTACACCGTGAGCAGCGGCGGCAG____GGAGGCGGAACCCGCGGCCGGAGACACACGCC GGGGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:139084225..139084314 26863196 MeRIP-seq:(Medium) rs1325523151 Functional Loss DEL dbSNP153 30..33 33 - - - 77825 RMVar_ID_77825 Human_SNP_ID_205750748 m1A Human chr4 - 139120194 139120194 139120194 GCTTTTTGACGCTTGTTCATGGTGATGGTAGCACATATGATTTGAGGAAGGCAAGACTGATGAAG GCTTTTTGACGCTTGTTCATGGTGATGGTAGCCCATATGATTTGAGGAAGGCAAGACTGATGAAG T G ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139120190..139120258 26863196 MeRIP-seq:(Medium) rs1249123537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15053811 RMVar_hsa_circ_228676,RMVar_hsa_circ_12262,RMVar_hsa_circ_96628,RMVar_hsa_circ_228670,RMVar_hsa_circ_228667,RMVar_hsa_circ_365851,RMVar_hsa_circ_228674,RMVar_hsa_circ_288745,RMVar_hsa_circ_366492,RMVar_hsa_circ_228682,RMVar_hsa_circ_81011,RMVar_hsa_circ_47514,RMVar_hsa_circ_269030,RMVar_hsa_circ_318390,RMVar_hsa_circ_228680,RMVar_hsa_circ_228684,RMVar_hsa_circ_278299,RMVar_hsa_circ_333983,RMVar_hsa_circ_228681,RMVar_hsa_circ_296032,RMVar_hsa_circ_228685,RMVar_hsa_circ_228683 77826 RMVar_ID_77826 Human_SNP_ID_205765210 m1A Human chr4 - 139176633 139176633 139176633 ACAGACCCCGGCGGGGGGGATGGGCCGAGCGCAGCTGGTCTCTCCGTGTTTACATCTCTGCGCGA ACAGACCCCGGCGGGGGGGATGGGCCGAGCGCTGCTGGTCTCTCCGTGTTTACATCTCTGCGCGA T A ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:139176605..139176744 26863196 MeRIP-seq:(Medium) rs1425011732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3747503,Human_RBP_ID_5326435,Human_RBP_ID_5394473,Human_RBP_ID_8130542,Human_RBP_ID_8211794,Human_RBP_ID_9436050,Human_RBP_ID_17409362,Human_RBP_ID_18501057,Human_RBP_ID_18955356,Human_RBP_ID_22418531,Human_RBP_ID_26791182 77827 RMVar_ID_77827 Human_SNP_ID_205765372 m1A Human chr4 + 139177161 139177138 139177162 CCCCGCGCAGCGACCCCCGCCCGCGCCGCCCCACCGACCCCCAACCGCCTAGGCGACGGCGGCGA CCCCGCGCAG________________________CGACCCCCAACCGCCTAGGCGACGGCGGCGA GCGACCCCCGCCCGCGCCGCCCCAC G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:139176969..139177200 26863196 MeRIP-seq:(Medium) rs1465542868 Functional Loss DEL dbSNP153 11..34 33 - - - 77828 RMVar_ID_77828 Human_SNP_ID_205765375 m1A Human chr4 + 139177141 139177141 139177141 GACAAAACAGAGGCTCGCCGCCCCGCGCAGCGACCCCCGCCCGCGCCGCCCCACCGACCCCCAAC GACAAAACAGAGGCTCGCCGCCCCGCGCAGCGCCCCCCGCCCGCGCCGCCCCACCGACCCCCAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139177091..139177196 26863196 MeRIP-seq:(Medium) rs920344176 Functional Loss SNV dbSNP153 33..33 33 - - - 77829 RMVar_ID_77829 Human_SNP_ID_205794529 m1A Human chr4 + 139295126 139295126 139295126 GTCAGGTTTGGCATTCGGCGGCTCTCGCACGTAGAACTTTGATCGCACTGAAGCTGAAAGGGGAA GTCAGGTTTGGCATTCGGCGGCTCTCGCACGTGGAACTTTGATCGCACTGAAGCTGAAAGGGGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139295076..139295173 26863196 MeRIP-seq:(Medium) rs1457472545 Functional Loss SNV dbSNP153 33..33 33 - - - 77830 RMVar_ID_77830 Human_SNP_ID_205794530 m1A Human chr4 + 139295126 139295126 139295126 GTCAGGTTTGGCATTCGGCGGCTCTCGCACGTAGAACTTTGATCGCACTGAAGCTGAAAGGGGAA GTCAGGTTTGGCATTCGGCGGCTCTCGCACGTTGAACTTTGATCGCACTGAAGCTGAAAGGGGAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139295076..139295173 26863196 MeRIP-seq:(Medium) rs1457472545 Functional Loss SNV dbSNP153 33..33 33 - - - 77831 RMVar_ID_77831 Human_SNP_ID_205794732 m1A Human chr4 + 139295758 139295758 139295758 ACTCACGGCCGCTCGGGAGCCTGGCGGGGGCCAGCAGCCGGGAAAGGGGACGCAGCAAGGCGGAC ACTCACGGCCGCTCGGGAGCCTGGCGGGGGCCCGCAGCCGGGAAAGGGGACGCAGCAAGGCGGAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:139295122..139295907 32194978 MeRIP-seq:(Medium) rs758866983 Functional Loss SNV dbSNP153 33..33 33 - - - 77832 RMVar_ID_77832 Human_SNP_ID_205794748 m1A Human chr4 + 139295783 139295783 139295783 GGGGGCCAGCAGCCGGGAAAGGGGACGCAGCAAGGCGGACGGCGCCATCTTGCGTGGCCCAGCTC GGGGGCCAGCAGCCGGGAAAGGGGACGCAGCACGGCGGACGGCGCCATCTTGCGTGGCCCAGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139295685..139295850 26863196 MeRIP-seq:(Medium) rs757027967 Functional Loss SNV dbSNP153 33..33 33 - - - 77833 RMVar_ID_77833 Human_SNP_ID_205794749 m1A Human chr4 + 139295783 139295783 139295783 GGGGGCCAGCAGCCGGGAAAGGGGACGCAGCAAGGCGGACGGCGCCATCTTGCGTGGCCCAGCTC GGGGGCCAGCAGCCGGGAAAGGGGACGCAGCAGGGCGGACGGCGCCATCTTGCGTGGCCCAGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139295685..139295850 26863196 MeRIP-seq:(Medium) rs757027967 Functional Loss SNV dbSNP153 33..33 33 - - - 77834 RMVar_ID_77834 Human_SNP_ID_205804890 m1A Human chr4 - 139334126 139334126 139334126 AGAAAAATTTAAGTTTAGCAAGGAATACAAACAACTTTAAATTCAACGCTAAATTTCTCTACTCT AGAAAAATTTAAGTTTAGCAAGGAATACAAACTACTTTAAATTCAACGCTAAATTTCTCTACTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139334121..139334193 26863196 MeRIP-seq:(Medium) rs576226080 Functional Loss SNV dbSNP153 33..33 33 - - - 77835 RMVar_ID_77835 Human_SNP_ID_205813548 m1A Human chr4 + 139370321 139370321 139370321 AGAAAAAAAATGCAGAAAAAGAAAAGCAGCAGAGAAATCAGAAAAAGAAGAAGGATGATGATGAT AGAAAAAAAATGCAGAAAAAGAAAAGCAGCAGCGAAATCAGAAAAAGAAGAAGGATGATGATGAT A C NAA15 Ensembl:ENSG00000164134 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139370271..139370356 26863196 MeRIP-seq:(Medium) rs1386790098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72010,Human_RBP_ID_213524,Human_RBP_ID_941024,Human_RBP_ID_17662017,Human_RBP_ID_18818814,Human_RBP_ID_19014591,Human_RBP_ID_24547728,Human_RBP_ID_26350328 Human_Splice_Rec_609517,Human_Splice_Rec_609555 RMVar_hsa_circ_121784,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_22637,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_51640,RMVar_hsa_circ_376577,RMVar_hsa_circ_27237,RMVar_hsa_circ_45370,RMVar_hsa_circ_102608,RMVar_hsa_circ_54256,RMVar_hsa_circ_228706,RMVar_hsa_circ_77949,RMVar_hsa_circ_228705,RMVar_hsa_circ_228707,RMVar_hsa_circ_311357,RMVar_hsa_circ_350026,RMVar_hsa_circ_355480,RMVar_hsa_circ_335029,RMVar_hsa_circ_228708 77836 RMVar_ID_77836 Human_SNP_ID_205813549 m1A Human chr4 + 139370321 139370321 139370321 AGAAAAAAAATGCAGAAAAAGAAAAGCAGCAGAGAAATCAGAAAAAGAAGAAGGATGATGATGAT AGAAAAAAAATGCAGAAAAAGAAAAGCAGCAGGGAAATCAGAAAAAGAAGAAGGATGATGATGAT A G NAA15 Ensembl:ENSG00000164134 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139370271..139370356 26863196 MeRIP-seq:(Medium) rs1386790098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72010,Human_RBP_ID_213524,Human_RBP_ID_941024,Human_RBP_ID_17662017,Human_RBP_ID_18818814,Human_RBP_ID_19014591,Human_RBP_ID_24547728,Human_RBP_ID_26350328 Human_Splice_Rec_609517,Human_Splice_Rec_609555 RMVar_hsa_circ_121784,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_22637,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_51640,RMVar_hsa_circ_376577,RMVar_hsa_circ_27237,RMVar_hsa_circ_45370,RMVar_hsa_circ_102608,RMVar_hsa_circ_54256,RMVar_hsa_circ_228706,RMVar_hsa_circ_77949,RMVar_hsa_circ_228705,RMVar_hsa_circ_228707,RMVar_hsa_circ_311357,RMVar_hsa_circ_350026,RMVar_hsa_circ_355480,RMVar_hsa_circ_335029,RMVar_hsa_circ_228708 77837 RMVar_ID_77837 Human_SNP_ID_205829927 m1A Human chr4 - 139440973 139440973 139440973 GAATTGCCCAGCGGAGCCCAGCCCAAATAGCCAATCTATAGCATTGTGACCCAAATAAATGCATG GAATTGCCCAGCGGAGCCCAGCCCAAATAGCCTATCTATAGCATTGTGACCCAAATAAATGCATG T A AC097376.3 Ensembl:ENSG00000273247 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139440928..139440998 26863196 MeRIP-seq:(Medium) rs894124528 Functional Loss SNV dbSNP153 33..33 33 - - - 77838 RMVar_ID_77838 Human_SNP_ID_205840107 m1A Human chr4 + 139482884 139482884 139482884 GGGACCAAAATTTGGATGCTACAAAGACAGGGACAATAGTAGCCAAGATAAATGCCCAGATGTTG GGGACCAAAATTTGGATGCTACAAAGACAGGGGCAATAGTAGCCAAGATAAATGCCCAGATGTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:139482840..139482972 26863196 MeRIP-seq:(Medium) rs1015093961 Functional Loss SNV dbSNP153 33..33 33 - - - 77839 RMVar_ID_77839 Human_SNP_ID_205845686 m1A Human chr4 + 139506353 139506353 139506353 ACCAAAGATGCTCGTTAACCGTGATGGGGTTAACTTTTGGTTGCAATAAATGCTGAAAGCATACC ACCAAAGATGCTCGTTAACCGTGATGGGGTTACCTTTTGGTTGCAATAAATGCTGAAAGCATACC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:139506302..139506403 32194978 MeRIP-seq:(Medium) rs1017893263 Functional Loss SNV dbSNP153 33..33 33 - - - 77840 RMVar_ID_77840 Human_SNP_ID_205846450 m1A Human chr4 + 139509891 139509891 139509891 GGTGAACCATTGGCTTAAGCTTTCAAGCAGGGATCCAACTGGATCTCCCTGAAACCACTGCCACC GGTGAACCATTGGCTTAAGCTTTCAAGCAGGGGTCCAACTGGATCTCCCTGAAACCACTGCCACC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:139509843..139509944 32194978 MeRIP-seq:(Medium) rs1392959045 Functional Loss SNV dbSNP153 33..33 33 - - - 77841 RMVar_ID_77841 Human_SNP_ID_205848945 m1A Human chr4 + 139520385 139520385 139520385 CCTTCTCCAGCACTGGAAATAAGAGATTCAGCAACATAAACCCTAAATTGAAAAAAGAGTTGAAT CCTTCTCCAGCACTGGAAATAAGAGATTCAGCCACATAAACCCTAAATTGAAAAAAGAGTTGAAT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:139520362..139529065 32194978 MeRIP-seq:(Medium) rs760328480 Functional Loss SNV dbSNP153 33..33 33 - - - 77842 RMVar_ID_77842 Human_SNP_ID_205855083 m1A Human chr4 - 139547030 139547025 139547030 TCCCTTTCTCCAGGGCACCTGGACGATGACGGATTACCGCACGGGTTCTGCACAGTCACCTACTC TCCCTTTCTCCAGGGCACCTGGACGATGACGG_____CGCACGGGTTCTGCACAGTCACCTACTC GGTAAT G SETD7 Ensembl:ENSG00000145391 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139546979..139547107 26863196 MeRIP-seq:(Medium) rs1340537692 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_1387599,Human_RBP_ID_7272079,Human_RBP_ID_8877489 Human_Splice_Rec_609626,Human_Splice_Rec_609644,Human_Splice_Rec_609658,Human_Splice_Rec_609664,Human_Splice_Rec_609672 RMVar_hsa_circ_324543,RMVar_hsa_circ_228713,RMVar_hsa_circ_13356,RMVar_hsa_circ_265635 77843 RMVar_ID_77843 Human_SNP_ID_205857259 m1A Human chr4 + 139556293 139556293 139556293 AGTCGGGGCTGGCTCGCACTGCCTCCCCCTACAGCCCTTTCAATTCCTTGGCCTTCAGCTGCTGC AGTCGGGGCTGGCTCGCACTGCCTCCCCCTACTGCCCTTTCAATTCCTTGGCCTTCAGCTGCTGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139556245..139556539 26863196 MeRIP-seq:(Medium) rs895474413 Functional Loss SNV dbSNP153 33..33 33 - - - 77844 RMVar_ID_77844 Human_SNP_ID_205857286 m1A Human chr4 - 139556380 139556380 139556380 CAGCAGCGGCAGCGGCCAAGGCGGCACACCGGAGCCTCCGAGGCGAGGGGCAAGTGGGCGAAGGG CAGCAGCGGCAGCGGCCAAGGCGGCACACCGGGGCCTCCGAGGCGAGGGGCAAGTGGGCGAAGGG T C SETD7 Ensembl:ENSG00000145391 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:139556270..139556506 26863196 MeRIP-seq:(Medium) rs942262562 Functional Loss SNV dbSNP153 33..33 33 - - - 77845 RMVar_ID_77845 Human_SNP_ID_205869482 m1A Human chr4 + 139606931 139606931 139606931 CAAGAAACAAGGTGGGGCTGCAGGGGTCAAGGAGATGGTGTCTGGGAAGTAACTGAGTCGCCTGG CAAGAAACAAGGTGGGGCTGCAGGGGTCAAGGCGATGGTGTCTGGGAAGTAACTGAGTCGCCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139606764..139606998 26863196 MeRIP-seq:(Medium) rs887666241 Functional Loss SNV dbSNP153 33..33 33 - - - 77846 RMVar_ID_77846 Human_SNP_ID_205869483 m1A Human chr4 + 139606931 139606931 139606931 CAAGAAACAAGGTGGGGCTGCAGGGGTCAAGGAGATGGTGTCTGGGAAGTAACTGAGTCGCCTGG CAAGAAACAAGGTGGGGCTGCAGGGGTCAAGGGGATGGTGTCTGGGAAGTAACTGAGTCGCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:139606764..139606998 26863196 MeRIP-seq:(Medium) rs887666241 Functional Loss SNV dbSNP153 33..33 33 - - - 77847 RMVar_ID_77847 Human_SNP_ID_205884080 m1A Human chr4 - 139665910 139665910 139665910 CGGGTAAACAAAGTTGGGGACCGGGTGGGGGGAAAAGGCTGATTCAAGCGGCTGAATGACCTTTG CGGGTAAACAAAGTTGGGGACCGGGTGGGGGGGAAAGGCTGATTCAAGCGGCTGAATGACCTTTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:139665859..139678581 26863196 MeRIP-seq:(Medium) rs987038389 Functional Loss SNV dbSNP153 33..33 33 - - - 77848 RMVar_ID_77848 Human_SNP_ID_205935776 m1A Human chr4 - 139889746 139889746 139889746 TAGTGCCTCCAATGGCAAACAACCTGCAGAAGACAACAATGAATAACTACCTCCCTCAGAATCAC TAGTGCCTCCAATGGCAAACAACCTGCAGAAGTCAACAATGAATAACTACCTCCCTCAGAATCAC T A MAML3 Ensembl:ENSG00000196782 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:139889695..139889810 26863196 MeRIP-seq:(Medium) rs1455380404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_24363,Human_miRNA_ID_28026,Human_miRNA_ID_492299,Human_miRNA_ID_495556,Human_miRNA_ID_1913649,Human_miRNA_ID_1916101,Human_miRNA_ID_1923463,Human_miRNA_ID_1925914,Human_miRNA_ID_1928364,Human_miRNA_ID_1930817,Human_miRNA_ID_2167940,Human_miRNA_ID_2169465,Human_miRNA_ID_2689108 RMVar_hsa_circ_103591,RMVar_hsa_circ_112807,RMVar_hsa_circ_228722,RMVar_hsa_circ_228726,RMVar_hsa_circ_110339,RMVar_hsa_circ_228724,RMVar_hsa_circ_228725,RMVar_hsa_circ_287333 77849 RMVar_ID_77849 Human_SNP_ID_205997617 m1A Human chr4 - 140154130 140154130 140154130 GGAGGAGGTGGAGGAGCGAGAGGAGGAGGAGGAGGCGGCGGCGGCGGCGGCGGCGAGCAGTTGAT GGAGGAGGTGGAGGAGCGAGAGGAGGAGGAGGCGGCGGCGGCGGCGGCGGCGGCGAGCAGTTGAT T G MAML3 Ensembl:ENSG00000196782 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:140154004..140154217 26863196 MeRIP-seq:(Medium) rs868585487 Functional Loss SNV dbSNP153 33..33 33 - - - 77850 RMVar_ID_77850 Human_SNP_ID_206050845 m1A Human chr4 - 140381380 140381379 140381380 CTTACTAATCCTATAATAAAAGACAGTGCTAAACCTACAAATTCAATAAAACATTCATCTTTAAG CTTACTAATCCTATAATAAAAGACAGTGCTAA_CCTACAAATTCAATAAAACATTCATCTTTAAG GT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:140381330..140381481 32194978 MeRIP-seq:(Medium) rs1194709166 Functional Loss DEL dbSNP153 33..33 33 - - - 77851 RMVar_ID_77851 Human_SNP_ID_206052841 m1A Human chr4 - 140390725 140390725 140390725 CTTTGCTTTTAACAAAATCTGTATTCTAGAAGAGGAAAGTGAACCTGAGGAAAAGAGTGAAGAAG CTTTGCTTTTAACAAAATCTGTATTCTAGAAGGGGAAAGTGAACCTGAGGAAAAGAGTGAAGAAG T C CLGN Ensembl:ENSG00000153132 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:140390596..140390782 26863196 MeRIP-seq:(Medium) rs1200982644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2821317,Human_RBP_ID_24547807 Human_Splice_Rec_609894,Human_Splice_Rec_609895,Human_Splice_Rec_609924,Human_Splice_Rec_609925 77852 RMVar_ID_77852 Human_SNP_ID_206087883 m1A Human chr4 + 140536908 140536908 140536908 TAGAAAGGTTTAGCGTATGGGGATCTTTTGATACATTGTGATGGAGAGAGGCAGGTCAGAACTTG TAGAAAGGTTTAGCGTATGGGGATCTTTTGATGCATTGTGATGGAGAGAGGCAGGTCAGAACTTG A G ELMOD2 Ensembl:ENSG00000179387 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:140536861..140536949 26863196 MeRIP-seq:(Medium) rs560252039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10713,RMVar_hsa_circ_339531,RMVar_hsa_circ_334682,RMVar_hsa_circ_298351,RMVar_hsa_circ_27643,RMVar_hsa_circ_228735,RMVar_hsa_circ_228736,RMVar_hsa_circ_29711,RMVar_hsa_circ_325042,RMVar_hsa_circ_228737,RMVar_hsa_circ_71523,RMVar_hsa_circ_296482,RMVar_hsa_circ_327995,RMVar_hsa_circ_228738 77853 RMVar_ID_77853 Human_SNP_ID_206114698 m1A Human chr4 - 140645501 140645500 140645501 ATAGAGGCTCTCGCAAGAGAGGATAGTGGCTTAGGGGTAGTTAAAAGTGGAGATGATAGCAGTGG ATAGAGGCTCTCGCAAGAGAGGATAGTGGCTT_GGGGTAGTTAAAAGTGGAGATGATAGCAGTGG CT C TBC1D9 Ensembl:ENSG00000109436 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:140645483..140645548 26863196 MeRIP-seq:(Medium) rs1367932598 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_14061,RMVar_hsa_circ_80093,RMVar_hsa_circ_92618,RMVar_hsa_circ_122876,RMVar_hsa_circ_85492,RMVar_hsa_circ_228742,RMVar_hsa_circ_76160,RMVar_hsa_circ_228744,RMVar_hsa_circ_228743,RMVar_hsa_circ_228740,RMVar_hsa_circ_228741,RMVar_hsa_circ_23328,RMVar_hsa_circ_328600,RMVar_hsa_circ_30178,RMVar_hsa_circ_346206,RMVar_hsa_circ_228746 77854 RMVar_ID_77854 Human_SNP_ID_206114699 m1A Human chr4 - 140645501 140645501 140645501 ATAGAGGCTCTCGCAAGAGAGGATAGTGGCTTAGGGGTAGTTAAAAGTGGAGATGATAGCAGTGG ATAGAGGCTCTCGCAAGAGAGGATAGTGGCTTTGGGGTAGTTAAAAGTGGAGATGATAGCAGTGG T A TBC1D9 Ensembl:ENSG00000109436 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:140645483..140645548 26863196 MeRIP-seq:(Medium) rs1021222944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14061,RMVar_hsa_circ_80093,RMVar_hsa_circ_92618,RMVar_hsa_circ_122876,RMVar_hsa_circ_85492,RMVar_hsa_circ_228742,RMVar_hsa_circ_76160,RMVar_hsa_circ_228744,RMVar_hsa_circ_228743,RMVar_hsa_circ_228740,RMVar_hsa_circ_228741,RMVar_hsa_circ_23328,RMVar_hsa_circ_328600,RMVar_hsa_circ_30178,RMVar_hsa_circ_346206,RMVar_hsa_circ_228746 77855 RMVar_ID_77855 Human_SNP_ID_206127638 m1A Human chr4 + 140701579 140701579 140701579 CAAGATTCGGTAAGGAGCGACCCGGGCGCTGGAGTCCAACACAACATCAAGGGTACCCACCAGCA CAAGATTCGGTAAGGAGCGACCCGGGCGCTGGGGTCCAACACAACATCAAGGGTACCCACCAGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:140701521..140756190 26863196 MeRIP-seq:(Medium) rs1335255196 Functional Loss SNV dbSNP153 33..33 33 - - - 77856 RMVar_ID_77856 Human_SNP_ID_206139767 m1A Human chr4 - 140755958 140755958 140755958 GGGCCAACCCATACTTCATCCTGCAGCGGAGGAAGGGCCACGCCGGCGATGGAGGCGGCGGCGGC GGGCCAACCCATACTTCATCCTGCAGCGGAGGCAGGGCCACGCCGGCGATGGAGGCGGCGGCGGC T G TBC1D9 Ensembl:ENSG00000109436 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:140755849..140756025 26863196 MeRIP-seq:(Medium) rs1389725779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248882,Human_RBP_ID_5531421,Human_RBP_ID_19013962 Human_Splice_Rec_610109 RMVar_hsa_circ_122876,RMVar_hsa_circ_228740,RMVar_hsa_circ_266357 77857 RMVar_ID_77857 Human_SNP_ID_206139821 m1A Human chr4 + 140756074 140756074 140756074 ACATGGTCCTGGCTGCCGCGGGCGGGCGCACAATGGGCCCGTGGGTCCAGTCCTGCACCCACCAC ACATGGTCCTGGCTGCCGCGGGCGGGCGCACAGTGGGCCCGTGGGTCCAGTCCTGCACCCACCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:140756027..140756338 26863196 MeRIP-seq:(Medium) rs1321096761 Functional Loss SNV dbSNP153 33..33 33 - - - 77858 RMVar_ID_77858 Human_SNP_ID_206139888 m1A Human chr4 + 140756303 140756303 140756303 CAGCATCCTCCCCGCGGCGTCGCCGCCCCGCGAGAGCCCGCGGCCGCAGACGCCCGGCCTGGCAC CAGCATCCTCCCCGCGGCGTCGCCGCCCCGCGGGAGCCCGCGGCCGCAGACGCCCGGCCTGGCAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:140756248..140756380 26863196 MeRIP-seq:(Medium) rs1338154467 Functional Loss SNV dbSNP153 33..33 33 - - - 77859 RMVar_ID_77859 Human_SNP_ID_206139932 m1A Human chr4 + 140756457 140756457 140756457 TATAGCTCAGTCCCGGGATCCGGCTCAGCGCCAGGCAGGGCTAAGGGCCACCCGAGCGGATTCGG TATAGCTCAGTCCCGGGATCCGGCTCAGCGCCGGGCAGGGCTAAGGGCCACCCGAGCGGATTCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:140756407..140756553 26863196 MeRIP-seq:(Medium) rs1219814169 Functional Loss SNV dbSNP153 33..33 33 - - - 77860 RMVar_ID_77860 Human_SNP_ID_206140032 m1A Human chr4 + 140756788 140756777 140756789 CGAGCTGAGCAGCTGTGGCTGGCTTCGGGGGAACCTTCGGGGGAAGCTCCTGGGGACCGTGTGCC CGAGCTGAGCAGCTGTGGCTGG____________CTTCGGGGGAAGCTCCTGGGGACCGTGTGCC GCTTCGGGGGAAC G AC096733.3 Ensembl:ENSG00000273472 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:140756665..140756795 26863196 MeRIP-seq:(Medium) rs1367232484 Functional Loss DEL dbSNP153 23..34 33 - - - 77861 RMVar_ID_77861 Human_SNP_ID_206194755 m1A Human chr4 + 140976330 140976330 140976330 TTTACAACCTTGTCCCATCTCTCCTTGCCACCATCTGCCAACCTCCTGTTATCTCCTCTTTCCCT TTTACAACCTTGTCCCATCTCTCCTTGCCACCGTCTGCCAACCTCCTGTTATCTCCTCTTTCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:140976323..140976459 26863196 MeRIP-seq:(Medium) rs1374366108 Functional Loss SNV dbSNP153 33..33 33 - - - 77862 RMVar_ID_77862 Human_SNP_ID_206225899 m1A Human chr4 - 141105936 141105936 141105936 TGCTAAAGAGGTTGGGTATTTTCTTCTGGGTAATAGGGAGGCATTAAAGGTTTTTGAGCAAGTAT TGCTAAAGAGGTTGGGTATTTTCTTCTGGGTAGTAGGGAGGCATTAAAGGTTTTTGAGCAAGTAT T C RNF150 Ensembl:ENSG00000170153 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:141105933..141106033 26863196 MeRIP-seq:(Medium) rs983538710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228759 77863 RMVar_ID_77863 Human_SNP_ID_206232070 m1A Human chr4 - 141132802 141132802 141132802 CGGGGAGGGGGCCCCGGCGGATAAAGATGGCAATGTCTCTCATCCAAGCGTGCTGCAGTCTGGCT CGGGGAGGGGGCCCCGGCGGATAAAGATGGCAGTGTCTCTCATCCAAGCGTGCTGCAGTCTGGCT T C RNF150 Ensembl:ENSG00000170153 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:141132751..141133100 26863196 MeRIP-seq:(Medium) rs770870862 Functional Loss SNV dbSNP153 33..33 33 - - - 77864 RMVar_ID_77864 Human_SNP_ID_206232138 m1A Human chr4 + 141132965 141132965 141132965 GGCCGCGGCCGGGACGCGCAGCCGCCGCGGGGACCGGATTCCGGGCGAGCGGATGGCGCTGGCCC GGCCGCGGCCGGGACGCGCAGCCGCCGCGGGGTCCGGATTCCGGGCGAGCGGATGGCGCTGGCCC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:141132863..141133125 26863196 MeRIP-seq:(Medium) rs954115243 Functional Loss SNV dbSNP153 33..33 33 - - - 77865 RMVar_ID_77865 Human_SNP_ID_206232212 m1A Human chr4 - 141133164 141133146 141133165 GGGGCTGGAGGGCGCAGGGCCGCCACCCTGCAAGTTCGTGGGCCCCCGGCCACCCTTATGAGAGA GGGGCTGGAGGGCGCAGGGCCGCCACCCTGC___________________CACCCTTATGAGAGA GGCCGGGGGCCCACGAACTT G RNF150 Ensembl:ENSG00000170153 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:141133019..141133225 26863196 MeRIP-seq:(Medium) rs1334783382 Functional Loss DEL dbSNP153 32..50 33 - - - 77866 RMVar_ID_77866 Human_SNP_ID_206232216 m1A Human chr4 - 141133164 141133164 141133164 GGGGCTGGAGGGCGCAGGGCCGCCACCCTGCAAGTTCGTGGGCCCCCGGCCACCCTTATGAGAGA GGGGCTGGAGGGCGCAGGGCCGCCACCCTGCATGTTCGTGGGCCCCCGGCCACCCTTATGAGAGA T A RNF150 Ensembl:ENSG00000170153 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:141133019..141133225 26863196 MeRIP-seq:(Medium) rs1371570160 Functional Loss SNV dbSNP153 33..33 33 - - - 77867 RMVar_ID_77867 Human_SNP_ID_206232310 m1A Human chr4 - 141133418 141133418 141133418 GACCGCTTACTCCGCTCTGCCTGCTCGCTCCCACTGTCCCCAAGCCCGCCCCGCCCGCGGCAAGT GACCGCTTACTCCGCTCTGCCTGCTCGCTCCCCCTGTCCCCAAGCCCGCCCCGCCCGCGGCAAGT T G RNF150 Ensembl:ENSG00000170153 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr4:141133250..141133475;chr4:141133319..141133447;chr4:141132499..141133475 26863196 MeRIP-seq:(Medium) rs1302385098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5448285,Human_RBP_ID_5475127 77868 RMVar_ID_77868 Human_SNP_ID_206253185 m1A Human chr4 + 141221077 141221077 141221077 GGCCCCCTGAGTGAGTCCGGTCTCCCGGCGAAAGTGAGCGAGGTTTGCCCGGAGCGCGCACGAGG GGCCCCCTGAGTGAGTCCGGTCTCCCGGCGAAGGTGAGCGAGGTTTGCCCGGAGCGCGCACGAGG A G ZNF330 Ensembl:ENSG00000109445 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:141221026..141221100 32194978 MeRIP-seq:(Medium) rs1382750593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4774527,Human_RBP_ID_5394889,Human_RBP_ID_19121839,Human_RBP_ID_22096004,Human_RBP_ID_22458454,Human_RBP_ID_24038069 Human_Splice_Rec_610223,Human_Splice_Rec_610225,Human_Splice_Rec_610243,Human_Splice_Rec_610275,Human_Splice_Rec_610279,Human_Splice_Rec_610301 77869 RMVar_ID_77869 Human_SNP_ID_206256201 m1A Human chr4 + 141233949 141233949 141233949 TTTGTTTACTAATTTGAATTTAGGAAGGACCTATGCTAGTGGCTATGCTCACTATGAGGAACAAG TTTGTTTACTAATTTGAATTTAGGAAGGACCTCTGCTAGTGGCTATGCTCACTATGAGGAACAAG A C ZNF330 Ensembl:ENSG00000109445 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:141233900..141234072 26863196 MeRIP-seq:(Medium) rs760892522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_614424,Human_RBP_ID_7273087,Human_RBP_ID_15060697,Human_RBP_ID_23034735,Human_RBP_ID_24038122,Human_RBP_ID_26350335,Human_RBP_ID_27566638 Human_miRNA_ID_867559 RMVar_hsa_circ_125689,RMVar_hsa_circ_228763 77870 RMVar_ID_77870 Human_SNP_ID_206256202 m1A Human chr4 + 141233949 141233949 141233949 TTTGTTTACTAATTTGAATTTAGGAAGGACCTATGCTAGTGGCTATGCTCACTATGAGGAACAAG TTTGTTTACTAATTTGAATTTAGGAAGGACCTGTGCTAGTGGCTATGCTCACTATGAGGAACAAG A G ZNF330 Ensembl:ENSG00000109445 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:141233900..141234072 26863196 MeRIP-seq:(Medium) rs760892522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_614424,Human_RBP_ID_7273087,Human_RBP_ID_15060697,Human_RBP_ID_23034735,Human_RBP_ID_24038122,Human_RBP_ID_26350335,Human_RBP_ID_27566638 Human_miRNA_ID_867559 RMVar_hsa_circ_125689,RMVar_hsa_circ_228763 77871 RMVar_ID_77871 Human_SNP_ID_206744404 m1A Human chr4 + 143206201 143206201 143206201 ACCTAGGAAATACATGTTATATGAACAGTGTTATACAAGCCTTGTTTATGGCCACAGAGTAAGTT ACCTAGGAAATACATGTTATATGAACAGTGTTGTACAAGCCTTGTTTATGGCCACAGAGTAAGTT A G USP38 Ensembl:ENSG00000170185 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:143206150..143206228 32194978 MeRIP-seq:(Medium) rs774511377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2822289 Human_Splice_Rec_610947,Human_Splice_Rec_610963,Human_Splice_Rec_610983 Human_miRNA_ID_289387,Human_miRNA_ID_527410,Human_miRNA_ID_879072 RMVar_hsa_circ_46035,RMVar_hsa_circ_228794,RMVar_hsa_circ_318267,RMVar_hsa_circ_266667,RMVar_hsa_circ_228795,RMVar_hsa_circ_334750 77872 RMVar_ID_77872 Human_SNP_ID_206744405 m1A Human chr4 + 143206201 143206201 143206201 ACCTAGGAAATACATGTTATATGAACAGTGTTATACAAGCCTTGTTTATGGCCACAGAGTAAGTT ACCTAGGAAATACATGTTATATGAACAGTGTTTTACAAGCCTTGTTTATGGCCACAGAGTAAGTT A T USP38 Ensembl:ENSG00000170185 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:143206150..143206228 32194978 MeRIP-seq:(Medium) rs774511377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2822289 Human_Splice_Rec_610947,Human_Splice_Rec_610963,Human_Splice_Rec_610983 Human_miRNA_ID_289387,Human_miRNA_ID_527410,Human_miRNA_ID_879072 RMVar_hsa_circ_46035,RMVar_hsa_circ_228794,RMVar_hsa_circ_318267,RMVar_hsa_circ_266667,RMVar_hsa_circ_228795,RMVar_hsa_circ_334750 77873 RMVar_ID_77873 Human_SNP_ID_206747761 m1A Human chr4 - 143220427 143220426 143220427 GGATCAAAATACGAGTCTGCCAACTGTATTAAATCCTCCTCCACCCCCTCCACCAGTTGGTCCAC GGATCAAAATACGAGTCTGCCAACTGTATTAA_TCCTCCTCCACCCCCTCCACCAGTTGGTCCAC AT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:143220376..143220474 32194978 MeRIP-seq:(Medium) rs1483010820 Functional Loss DEL dbSNP153 33..33 33 - - - 77874 RMVar_ID_77874 Human_SNP_ID_206775685 m1A Human chr4 + 143336276 143336274 143336277 CTGAACGTGGGAAGGGGAGGAGGAGAGGGAGGAAGAAGGAGCCCGGCGGCCGGGAGAGGGAGGGA CTGAACGTGGGAAGGGGAGGAGGAGAGGGAG___GAAGGAGCCCGGCGGCCGGGAGAGGGAGGGA GGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:143336230..143336363 26863196 MeRIP-seq:(Medium) rs1318978834 Functional Loss DEL dbSNP153 32..34 33 - - - 77875 RMVar_ID_77875 Human_SNP_ID_206793958 m1A Human chr4 + 143415428 143415428 143415428 AAATCAGTTTGATAAATGTGCATCTTCTTGAAAACATTATCTCAAGTTAATACTGAATGGATATT AAATCAGTTTGATAAATGTGCATCTTCTTGAAGACATTATCTCAAGTTAATACTGAATGGATATT A G GAB1 Ensembl:ENSG00000109458 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:143415425..143415524 26863196 MeRIP-seq:(Medium) rs779376626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117192,RMVar_hsa_circ_228797 77876 RMVar_ID_77876 Human_SNP_ID_206816506 m1A Human chr4 - 143513638 143513638 143513638 GGGTGGGCGGGGCCAGACGGGTCACTGAGGTCAAGGAAGGCCGGCTGATTTAGAGAAGGGCGGAG GGGTGGGCGGGGCCAGACGGGTCACTGAGGTCGAGGAAGGCCGGCTGATTTAGAGAAGGGCGGAG T C SMARCA5-AS1 Ensembl:ENSG00000245112 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:143513536..143513651 26863410 MeRIP-seq:(Medium) rs1342529019 Functional Loss SNV dbSNP153 33..33 33 - - - 77877 RMVar_ID_77877 Human_SNP_ID_206816568 m1A Human chr4 + 143513770 143513770 143513770 GTTTGGGAGTGTGCAGCTCCTGGGCCCGGCTCAGGCCCGTCGCGGAGGCGCGGCGCAGGGGAGCG GTTTGGGAGTGTGCAGCTCCTGGGCCCGGCTCGGGCCCGTCGCGGAGGCGCGGCGCAGGGGAGCG A G SMARCA5 Ensembl:ENSG00000153147 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:143513726..143513925 26863196 MeRIP-seq:(Medium) rs916872715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249485,Human_RBP_ID_1315779,Human_RBP_ID_4794718,Human_RBP_ID_5531422,Human_RBP_ID_9335082,Human_RBP_ID_9396696,Human_RBP_ID_22458455,Human_RBP_ID_26349593,Human_RBP_ID_27825100 RMVar_hsa_circ_269622 77878 RMVar_ID_77878 Human_SNP_ID_206816580 m1A Human chr4 - 143513809 143513795 143513809 TCGCAATAAACTGGTGGAGGAGCGAGACTCCCACCCGAGCGCTCCCCTGCGCCGCGCCTCCGCGA TCGCAATAAACTGGTGGAGGAGCGAGACTCCC______________CTGCGCCGCGCCTCCGCGA GGGGAGCGCTCGGGT G SMARCA5-AS1 Ensembl:ENSG00000245112 lincRNA exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:143513769..143513869 26863410 MeRIP-seq:(Medium) rs1457823973 Functional Loss DEL dbSNP153 33..46 33 - - - 77879 RMVar_ID_77879 Human_SNP_ID_206816617 m1A Human chr4 - 143513869 143513865 143513869 TGCTGCCAGAGGCCCGAGTCCGGCGGGGATGGACGGGGAGGCCTAGGCCTGGATGCTACGTCGCA TGCTGCCAGAGGCCCGAGTCCGGCGGGGATGG____GGAGGCCTAGGCCTGGATGCTACGTCGCA CCCGT C SMARCA5-AS1 Ensembl:ENSG00000245112 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:143513676..143513975 26863196 MeRIP-seq:(Medium) rs1259011893 Functional Loss DEL dbSNP153 33..36 33 - - - 77880 RMVar_ID_77880 Human_SNP_ID_207206352 m1A Human chr4 + 145054850 145054850 145054850 GTTCTTTCTCCTTGTTATGTATCTACCCTCGCATCTATTTTATTCATTCTACACCATTCTGTGTC GTTCTTTCTCCTTGTTATGTATCTACCCTCGCTTCTATTTTATTCATTCTACACCATTCTGTGTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:145054807..145054927 26863196 MeRIP-seq:(Medium) rs966571576 Functional Loss SNV dbSNP153 33..33 33 - - - 77881 RMVar_ID_77881 Human_SNP_ID_207206355 m1A Human chr4 + 145054854 145054854 145054854 TTTCTCCTTGTTATGTATCTACCCTCGCATCTATTTTATTCATTCTACACCATTCTGTGTCTTCC TTTCTCCTTGTTATGTATCTACCCTCGCATCTCTTTTATTCATTCTACACCATTCTGTGTCTTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145054829..145054984 26863196 MeRIP-seq:(Medium) rs540123382 Functional Loss SNV dbSNP153 33..33 33 - - - 77882 RMVar_ID_77882 Human_SNP_ID_207206356 m1A Human chr4 + 145054854 145054854 145054854 TTTCTCCTTGTTATGTATCTACCCTCGCATCTATTTTATTCATTCTACACCATTCTGTGTCTTCC TTTCTCCTTGTTATGTATCTACCCTCGCATCTGTTTTATTCATTCTACACCATTCTGTGTCTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145054829..145054984 26863196 MeRIP-seq:(Medium) rs540123382 Functional Loss SNV dbSNP153 33..33 33 - - - 77883 RMVar_ID_77883 Human_SNP_ID_207217502 m1A Human chr4 + 145102709 145102709 145102709 ATAAAAACACCAAGAGCTGAGGGACAGTGGAAATATGATAGAATCAAGAGATAATGAAAGGTTTG ATAAAAACACCAAGAGCTGAGGGACAGTGGAAGTATGATAGAATCAAGAGATAATGAAAGGTTTG A G ABCE1 Ensembl:ENSG00000164163 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145102704..145103031 26863196 MeRIP-seq:(Medium) rs1363907896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15063896 RMVar_hsa_circ_85914,RMVar_hsa_circ_228838 77884 RMVar_ID_77884 Human_SNP_ID_207237604 m1A Human chr4 + 145180356 145180356 145180356 TTTCCTCCTCCGTACCGGTGTGAAGCGAGAAAACCCCCGCCCCTGGCGCGCACGCTGGGCCGGCT TTTCCTCCTCCGTACCGGTGTGAAGCGAGAAACCCCCCGCCCCTGGCGCGCACGCTGGGCCGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:145180310..145180532 26863196 MeRIP-seq:(Medium) rs977959034 Functional Loss SNV dbSNP153 33..33 33 - - - 77885 RMVar_ID_77885 Human_SNP_ID_207313369 m1A Human chr4 - 145489902 145489902 145489902 TCTTCCAGTTTCTTCTTTGGTCTATGTCAAACAGCCTCTCAGGCAGTCTACTTCAAATTAGCCTC TCTTCCAGTTTCTTCTTTGGTCTATGTCAAACGGCCTCTCAGGCAGTCTACTTCAAATTAGCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145489892..145489985 26863196 MeRIP-seq:(Medium) rs1450503604 Functional Loss SNV dbSNP153 33..33 33 - - - 77886 RMVar_ID_77886 Human_SNP_ID_207324934 m1A Human chr4 - 145540015 145540015 145540015 GGGCTTCCTGGGTCTGAGCTGGTGGGAGAGTGAGGGTAGGTGCTGCTGCTGCTCCCAGGAGAGTT GGGCTTCCTGGGTCTGAGCTGGTGGGAGAGTGGGGGTAGGTGCTGCTGCTGCTCCCAGGAGAGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145539965..145540090 26863196 MeRIP-seq:(Medium) rs1034362615 Functional Loss SNV dbSNP153 33..33 33 - - - 77887 RMVar_ID_77887 Human_SNP_ID_207325516 m1A Human chr4 + 145542533 145542533 145542533 TTTCAGTACAGAAGAGGATACGTGTTTTGAGCATGTATGTTTACTAAGGGTTAAGAAATAACTTC TTTCAGTACAGAAGAGGATACGTGTTTTGAGCGTGTATGTTTACTAAGGGTTAAGAAATAACTTC A G SMAD1 Ensembl:ENSG00000170365 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145542531..145542599 26863196 MeRIP-seq:(Medium) rs111738894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228858,RMVar_hsa_circ_81302,RMVar_hsa_circ_358346,RMVar_hsa_circ_110653,RMVar_hsa_circ_228859,RMVar_hsa_circ_228860 77888 RMVar_ID_77888 Human_SNP_ID_207325556 m1A Human chr4 + 145542630 145542630 145542630 TGCTTACCTGCCTCCTGAAGACCCCATGACCCAGGATGGCTCTCAGCCGATGGACACAAACATGA TGCTTACCTGCCTCCTGAAGACCCCATGACCCGGGATGGCTCTCAGCCGATGGACACAAACATGA A G SMAD1 Ensembl:ENSG00000170365 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:145542546..145542632 26863196 MeRIP-seq:(Medium) rs746555376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_612402,Human_Splice_Rec_612403,Human_Splice_Rec_612426,Human_Splice_Rec_612427,Human_Splice_Rec_612438,Human_Splice_Rec_612439 Human_miRNA_ID_2039091,Human_miRNA_ID_3018071 RMVar_hsa_circ_228858,RMVar_hsa_circ_81302,RMVar_hsa_circ_358346,RMVar_hsa_circ_110653,RMVar_hsa_circ_228859,RMVar_hsa_circ_228860 77889 RMVar_ID_77889 Human_SNP_ID_207344539 m1A Human chr4 + 145619240 145619240 145619240 GGAGACCTTCACGCTCACTCGCTCTCCGCCACACGCCGGAACTGCGCGGCCACGTCCACGGGGAC GGAGACCTTCACGCTCACTCGCTCTCCGCCACGCGCCGGAACTGCGCGGCCACGTCCACGGGGAC A G MMAA Ensembl:ENSG00000151611 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:145619194..145619339 26863196 MeRIP-seq:(Medium) rs372213583 Functional Loss SNV dbSNP153 33..33 33 - - - 77890 RMVar_ID_77890 Human_SNP_ID_207419686 m1A Human chr4 + 145937399 145937399 145937399 AGCCCGAGTCTCGCCCGGCTCCGTCTGCTCCGACTGACCCCGCATTTTATTGCGGCCAGGAGCCC AGCCCGAGTCTCGCCCGGCTCCGTCTGCTCCGGCTGACCCCGCATTTTATTGCGGCCAGGAGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:145937393..145937528 26863196 MeRIP-seq:(Medium) rs1173945355 Functional Loss SNV dbSNP153 33..33 33 - - - 77891 RMVar_ID_77891 Human_SNP_ID_207419827 m1A Human chr4 + 145937742 145937742 145937742 CCGCCTCCTCCACCTCCGCCTCCTCCTGCTCCAGCCGCCGCCGCCGCTGCCGCCGGCGGCTCGGG CCGCCTCCTCCACCTCCGCCTCCTCCTGCTCCGGCCGCCGCCGCCGCTGCCGCCGGCGGCTCGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:145937740..145937827 26863196 MeRIP-seq:(Medium) rs1360835799 Functional Loss SNV dbSNP153 33..33 33 - - - 77892 RMVar_ID_77892 Human_SNP_ID_207483119 m1A Human chr4 + 146182972 146182972 146182972 ACCCCTAGTGACTTCTTAAAGCAAATCATCGGACGACCAGTTGTGGTAAAATTAAATTCTGGAGT ACCCCTAGTGACTTCTTAAAGCAAATCATCGGGCGACCAGTTGTGGTAAAATTAAATTCTGGAGT A G LSM6 Ensembl:ENSG00000164167 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:146182870..146183025 26863196 MeRIP-seq:(Medium) rs1263516015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283143,Human_RBP_ID_614740,Human_RBP_ID_1035423,Human_RBP_ID_1387671,Human_RBP_ID_1635673,Human_RBP_ID_1973518,Human_RBP_ID_3729976,Human_RBP_ID_4795158,Human_RBP_ID_5475158,Human_RBP_ID_15066187,Human_RBP_ID_18819281 Human_Splice_Rec_613012,Human_Splice_Rec_613013,Human_Splice_Rec_613020,Human_Splice_Rec_613021,Human_Splice_Rec_613026,Human_Splice_Rec_613027,Human_Splice_Rec_613032,Human_Splice_Rec_613033,Human_Splice_Rec_613038,Human_Splice_Rec_613039,Human_Splice_Rec_613047 RMVar_hsa_circ_43647,RMVar_hsa_circ_64106 77893 RMVar_ID_77893 Human_SNP_ID_207776404 m1A Human chr4 + 147426250 147426250 147426250 GCCTGAGGGGCACGCTTCTTGAAGCCCACTCCATGGATGCACTTGTGAATGTTGATGGTGTATTC GCCTGAGGGGCACGCTTCTTGAAGCCCACTCCGTGGATGCACTTGTGAATGTTGATGGTGTATTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:147426199..147426264 26863196 MeRIP-seq:(Medium) rs930050240 Functional Loss SNV dbSNP153 33..33 33 - - - 77894 RMVar_ID_77894 Human_SNP_ID_207776405 m1A Human chr4 + 147426250 147426250 147426250 GCCTGAGGGGCACGCTTCTTGAAGCCCACTCCATGGATGCACTTGTGAATGTTGATGGTGTATTC GCCTGAGGGGCACGCTTCTTGAAGCCCACTCCTTGGATGCACTTGTGAATGTTGATGGTGTATTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:147426199..147426264 26863196 MeRIP-seq:(Medium) rs930050240 Functional Loss SNV dbSNP153 33..33 33 - - - 77895 RMVar_ID_77895 Human_SNP_ID_207790432 m1A Human chr4 - 147481133 147481133 147481133 CGACGACCGGGTGGGATGGATGAAGCCTCTCCACCGCCTCTCCACAATCGTCAGACCAGCGGGAT CGACGACCGGGTGGGATGGATGAAGCCTCTCCGCCGCCTCTCCACAATCGTCAGACCAGCGGGAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:147480995..147481199 26863196 MeRIP-seq:(Medium) rs1433390186 Functional Loss SNV dbSNP153 33..33 33 - - - 77896 RMVar_ID_77896 Human_SNP_ID_207849207 m1A Human chr4 + 147731968 147731968 147731968 GGGAAGGGAGGAAGAAGGAAGGCGGAGGAAAGAGAAGGGGACGAGCGGGAGCGCGGGCCCGGCCG GGGAAGGGAGGAAGAAGGAAGGCGGAGGAAAGCGAAGGGGACGAGCGGGAGCGCGGGCCCGGCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:147731917..147732224 26863196 MeRIP-seq:(Medium) rs1229233536 Functional Loss SNV dbSNP153 33..33 33 - - - 77897 RMVar_ID_77897 Human_SNP_ID_207852652 m1A Human chr4 + 147744392 147744392 147744392 GGATAAGAATGGTGCTGTCGAGGGGGTGGGGGAGGGTCAAGAAGGCCCTTGGAAAGCAGGTTGAG GGATAAGAATGGTGCTGTCGAGGGGGTGGGGGGGGGTCAAGAAGGCCCTTGGAAAGCAGGTTGAG A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:147744270..147744600 26863196 MeRIP-seq:(Medium) rs1485321258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228915,RMVar_hsa_circ_79750 77898 RMVar_ID_77898 Human_SNP_ID_207855819 m1A Human chr4 - 147756933 147756933 147756933 CCTCAAGGTGAGCCTTTTCCATTATACCAGGCATTCATGAATGCCCTTCCCTCTTCTTATAATCT CCTCAAGGTGAGCCTTTTCCATTATACCAGGCGTTCATGAATGCCCTTCCCTCTTCTTATAATCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:147756928..147757076 26863196 MeRIP-seq:(Medium) rs1184269044 Functional Loss SNV dbSNP153 33..33 33 - - - 77899 RMVar_ID_77899 Human_SNP_ID_207879770 m1A Human chr4 - 147850065 147850065 147850065 TAGACACAGAGTGCTGGTTGGTGTGTTTTTACAGAGTGCTGATTGGTGCATTTACAAACCTTTGG TAGACACAGAGTGCTGGTTGGTGTGTTTTTACTGAGTGCTGATTGGTGCATTTACAAACCTTTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:147849952..147850120 26863196 MeRIP-seq:(Medium) rs756039337 Functional Loss SNV dbSNP153 33..33 33 - - - 77900 RMVar_ID_77900 Human_SNP_ID_207932933 m1A Human chr4 + 148062057 148062057 148062057 AAGGCAAAGCTTGAGGCGGAGGTGGGAACGCCAGGAAGCAGAGCTGTGGCAGACAGGGTAGGCTG AAGGCAAAGCTTGAGGCGGAGGTGGGAACGCCGGGAAGCAGAGCTGTGGCAGACAGGGTAGGCTG A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:148061941..148062182 26863196 MeRIP-seq:(Medium) rs920316017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100243,RMVar_hsa_circ_121902,RMVar_hsa_circ_228916,RMVar_hsa_circ_228923,RMVar_hsa_circ_46775,RMVar_hsa_circ_95410,RMVar_hsa_circ_228933,RMVar_hsa_circ_100140,RMVar_hsa_circ_107190,RMVar_hsa_circ_228942,RMVar_hsa_circ_111243,RMVar_hsa_circ_76535,RMVar_hsa_circ_24369,RMVar_hsa_circ_228944,RMVar_hsa_circ_228943,RMVar_hsa_circ_313736,RMVar_hsa_circ_228954 77901 RMVar_ID_77901 Human_SNP_ID_207932934 m1A Human chr4 + 148062057 148062057 148062057 AAGGCAAAGCTTGAGGCGGAGGTGGGAACGCCAGGAAGCAGAGCTGTGGCAGACAGGGTAGGCTG AAGGCAAAGCTTGAGGCGGAGGTGGGAACGCCTGGAAGCAGAGCTGTGGCAGACAGGGTAGGCTG A T ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:148061941..148062182 26863196 MeRIP-seq:(Medium) rs920316017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100243,RMVar_hsa_circ_121902,RMVar_hsa_circ_228916,RMVar_hsa_circ_228923,RMVar_hsa_circ_46775,RMVar_hsa_circ_95410,RMVar_hsa_circ_228933,RMVar_hsa_circ_100140,RMVar_hsa_circ_107190,RMVar_hsa_circ_228942,RMVar_hsa_circ_111243,RMVar_hsa_circ_76535,RMVar_hsa_circ_24369,RMVar_hsa_circ_228944,RMVar_hsa_circ_228943,RMVar_hsa_circ_313736,RMVar_hsa_circ_228954 77902 RMVar_ID_77902 Human_SNP_ID_245002972 m1A Human chr5 + 107380835 107380835 107380835 GAGAAGGCATAAATATTGCATAGGAGAGCAAAACCCTCCCAGCCCTAGCCAGCGCTGGCTGCATC GAGAAGGCATAAATATTGCATAGGAGAGCAAACCCCTCCCAGCCCTAGCCAGCGCTGGCTGCATC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:107380784..107380871 32194978 MeRIP-seq:(Medium) rs982998335 Functional Loss SNV dbSNP153 33..33 33 - - - 77903 RMVar_ID_77903 Human_SNP_ID_245255676 m1A Human chr5 - 108381002 108381002 108381002 TGCGGCGGCGGCGGCGGCGGCGGTGGCGGGGGAGGGCCTGCGGGGGGAGGCGCTTCGCCGCCCCG TGCGGCGGCGGCGGCGGCGGCGGTGGCGGGGGGGGGCCTGCGGGGGGAGGCGCTTCGCCGCCCCG T C FBXL17 Ensembl:ENSG00000145743 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:108380901..108381002 26863196 MeRIP-seq:(Medium) rs918117623 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_107579,RMVar_hsa_circ_233567 77904 RMVar_ID_77904 Human_SNP_ID_245255861 m1A Human chr5 + 108381358 108381358 108381358 GGATAGCAGGAAGCGGCGGGCAGCAGCGGCGCAGTCCTCGGCGGCCAGGGCCGCGTAGCGCCGCG GGATAGCAGGAAGCGGCGGGCAGCAGCGGCGCTGTCCTCGGCGGCCAGGGCCGCGTAGCGCCGCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:108381311..108381445 26863196 MeRIP-seq:(Medium) rs529903704 Functional Loss SNV dbSNP153 33..33 33 - - - 77905 RMVar_ID_77905 Human_SNP_ID_245255935 m1A Human chr5 + 108381491 108381491 108381491 TCCTCTGGGCCGGCGGGGGCGGGCGCGCCGGGACTGTGCACGATGAAGCAGAGCATGCAGGGCCC TCCTCTGGGCCGGCGGGGGCGGGCGCGCCGGGGCTGTGCACGATGAAGCAGAGCATGCAGGGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:108381440..108381694 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 77906 RMVar_ID_77906 Human_SNP_ID_245255955 m1A Human chr5 - 108381544 108381544 108381544 CCAAGGTGCCCCCTCAGCCGGCGGCGCCCCGGAGCCGGGACTGCTTCTTCCGCGGGCCCTGCATG CCAAGGTGCCCCCTCAGCCGGCGGCGCCCCGGGGCCGGGACTGCTTCTTCCGCGGGCCCTGCATG T C FBXL17 Ensembl:ENSG00000145743 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:108381499..108381600 26863196 MeRIP-seq:(Medium) rs1027754546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107579,RMVar_hsa_circ_233567 77907 RMVar_ID_77907 Human_SNP_ID_245256165 m1A Human chr5 + 108381948 108381948 108381948 GGAGAACGATGGGCGCGAGCTTTGGGGACGCGAGGGAGGGAGCGAGCGAGCCTGCCGGCTAGGCG GGAGAACGATGGGCGCGAGCTTTGGGGACGCGGGGGAGGGAGCGAGCGAGCCTGCCGGCTAGGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:108381898..108382027 26863196 MeRIP-seq:(Medium) rs1003911614 Functional Loss SNV dbSNP153 33..33 33 - - - 77908 RMVar_ID_77908 Human_SNP_ID_245474253 m1A Human chr5 + 109193028 109193028 109193028 TAAAATGACCCATAGCCAACAATAAATGCAATAACAATAAAGGAAACTAACCCTCACAAAGGGTT TAAAATGACCCATAGCCAACAATAAATGCAATGACAATAAAGGAAACTAACCCTCACAAAGGGTT A G FER Ensembl:ENSG00000151422 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11738705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17526043 GWAS_ID_9308,GWAS_ID_9309,GWAS_ID_9310 77909 RMVar_ID_77909 Human_SNP_ID_245534538 m1A Human chr5 + 109409852 109409852 109409852 AAAAAAAAAAAAAAACCCTCACCGAAATGTGCAGCGGCTCCGGAGCGAGAACAGCGCTCGAACCT AAAAAAAAAAAAAAACCCTCACCGAAATGTGCCGCGGCTCCGGAGCGAGAACAGCGCTCGAACCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:109409851..109409900 32194978 MeRIP-seq:(Medium) rs1194739771 Functional Loss SNV dbSNP153 33..33 33 - - - 77910 RMVar_ID_77910 Human_SNP_ID_245534551 m1A Human chr5 + 109409887 109409887 109409887 GGCTCCGGAGCGAGAACAGCGCTCGAACCTCCACCCGCCACCACCGCCTTCTTCTCCGCCTCCAA GGCTCCGGAGCGAGAACAGCGCTCGAACCTCCCCCCGCCACCACCGCCTTCTTCTCCGCCTCCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:109409797..109409905;chr5:109409799..109409901;chr5:109409802..109409903 26863196 MeRIP-seq:(Medium) rs900469488 Functional Loss SNV dbSNP153 33..33 33 - - - 77911 RMVar_ID_77911 Human_SNP_ID_245609606 m1A Human chr5 - 109689861 109689861 109689861 CTGGGCGGGACGGTCGGGCCCGCCCCCGCGGCACCGGCACCGCCCCCGCCTACCCCGACTGAGCC CTGGGCGGGACGGTCGGGCCCGCCCCCGCGGCTCCGGCACCGCCCCCGCCTACCCCGACTGAGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:109689824..109689899 26863196 MeRIP-seq:(Medium) rs1561460437 Functional Loss SNV dbSNP153 33..33 33 - - - 77912 RMVar_ID_77912 Human_SNP_ID_245910748 m1A Human chr5 - 110739080 110739068 110739080 GGGGCAGGATGACGCGAGCCCGCCCGGAGCCCACCACCACCGGGGCCACCACGACCTAAGCACAC GGGGCAGGATGACGCGAGCCCGCCCGGAGCCC____________GCCACCACGACCTAAGCACAC CCCCGGTGGTGGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:110739031..110739381 26863196 MeRIP-seq:(Medium) rs1260265001 Functional Loss DEL dbSNP153 33..44 33 - - - 77913 RMVar_ID_77913 Human_SNP_ID_245910760 m1A Human chr5 - 110739074 110739074 110739074 GGATGACGCGAGCCCGCCCGGAGCCCACCACCACCGGGGCCACCACGACCTAAGCACACACAGCT GGATGACGCGAGCCCGCCCGGAGCCCACCACCGCCGGGGCCACCACGACCTAAGCACACACAGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:110739026..110739179 26863196 MeRIP-seq:(Medium) rs748696438 Functional Loss SNV dbSNP153 33..33 33 - - - 77914 RMVar_ID_77914 Human_SNP_ID_245910763 m1A Human chr5 - 110739080 110739080 110739080 GGGGCAGGATGACGCGAGCCCGCCCGGAGCCCACCACCACCGGGGCCACCACGACCTAAGCACAC GGGGCAGGATGACGCGAGCCCGCCCGGAGCCCGCCACCACCGGGGCCACCACGACCTAAGCACAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:110739031..110739381 26863196 MeRIP-seq:(Medium) rs1382299402 Functional Loss SNV dbSNP153 33..33 33 - - - 77915 RMVar_ID_77915 Human_SNP_ID_245910889 m1A Human chr5 + 110739298 110739298 110739298 CCCCGGCAGCCGCAACCTGCACTGGGGCGAGAAGAGCCCGCCCTACGGCGTGCCCACCACCTCCA CCCCGGCAGCCGCAACCTGCACTGGGGCGAGAGGAGCCCGCCCTACGGCGTGCCCACCACCTCCA A G SLC25A46 Ensembl:ENSG00000164209 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:110739257..110739353 26863196 MeRIP-seq:(Medium) rs759961883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4803384,Human_RBP_ID_18829693,Human_RBP_ID_24075948 77916 RMVar_ID_77916 Human_SNP_ID_245916554 m1A Human chr5 - 110761773 110761773 110761773 TACTCAGTGAAGGAACCTAAATCTCAAATGTTATTTTGAAGAAGTGTAGAGTAAATAATTTTGGT TACTCAGTGAAGGAACCTAAATCTCAAATGTTGTTTTGAAGAAGTGTAGAGTAAATAATTTTGGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:110761722..110761805 32194978 MeRIP-seq:(Medium) rs776771749 Functional Loss SNV dbSNP153 33..33 33 - - - 77917 RMVar_ID_77917 Human_SNP_ID_246007540 m1A Human chr5 + 111073513 111073513 111073513 TTTCTCGTAAACTTTGCCGCCTATGAGCAGCCACATTGCCTTACTGAAATCCAGAGCCTAACCTT TTTCTCGTAAACTTTGCCGCCTATGAGCAGCCCCATTGCCTTACTGAAATCCAGAGCCTAACCTT A C TSLP Ensembl:ENSG00000145777 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:111073463..111073560 26863196 MeRIP-seq:(Medium) rs771611770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_628248 Human_Splice_Rec_679750,Human_Splice_Rec_679756 77918 RMVar_ID_77918 Human_SNP_ID_246122882 m1A Human chr5 + 111499165 111499165 111499165 TGAATTGCCTCAAGTTCCCATTTTAGAAGTAAACTAGATGGAGAGTTCAAAACCCAAAGTCATTT TGAATTGCCTCAAGTTCCCATTTTAGAAGTAATCTAGATGGAGAGTTCAAAACCCAAAGTCATTT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:111499118..111499197 32194978 MeRIP-seq:(Medium) rs1246224588 Functional Loss SNV dbSNP153 33..33 33 - - - 77919 RMVar_ID_77919 Human_SNP_ID_246122948 m1A Human chr5 - 111499560 111499560 111499560 TCTACCTCAGCCTCCTGAATAGCTGGGAATACAGGTGCACGCCACTATGCATGGCTAATTTTTGT TCTACCTCAGCCTCCTGAATAGCTGGGAATACGGGTGCACGCCACTATGCATGGCTAATTTTTGT T C STARD4 Ensembl:ENSG00000164211 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:111499514..111499615 32194978 MeRIP-seq:(Medium) rs1161185128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_628449,Human_RBP_ID_7364366 Human_miRNA_ID_1400358,Human_miRNA_ID_1473236 77920 RMVar_ID_77920 Human_SNP_ID_246126026 m1A Human chr5 - 111512208 111512208 111512208 CGGGCCCCGGCGTCCGGGCGGGAGAGGACCTCACAGATGAAAGAGAAACCTGAGCCCCTGGGAGG CGGGCCCCGGCGTCCGGGCGGGAGAGGACCTCGCAGATGAAAGAGAAACCTGAGCCCCTGGGAGG T C STARD4 Ensembl:ENSG00000164211 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:111512205..111512411 32194978 MeRIP-seq:(Medium) rs1246824041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5396117 RMVar_hsa_circ_94620,RMVar_hsa_circ_233706 77921 RMVar_ID_77921 Human_SNP_ID_246126097 m1A Human chr5 - 111512450 111512450 111512450 GGCGGGCCGGGAGGCTGAGCAGTACTGTTGAGAGCGGTGTGAGGTGCTTGGTAGCGCGCCGTAGC GGCGGGCCGGGAGGCTGAGCAGTACTGTTGAGTGCGGTGTGAGGTGCTTGGTAGCGCGCCGTAGC T A STARD4 Ensembl:ENSG00000164211 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:111512218..111512490 26863196 MeRIP-seq:(Medium) rs1177747847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_628465,Human_RBP_ID_788861,Human_RBP_ID_943414,Human_RBP_ID_4845292,Human_RBP_ID_9335279,Human_RBP_ID_9398049,Human_RBP_ID_17415271,Human_RBP_ID_18829824,Human_RBP_ID_22100124,Human_RBP_ID_23050153 Human_Splice_Rec_680079,Human_Splice_Rec_680089,Human_Splice_Rec_680097,Human_Splice_Rec_680105,Human_Splice_Rec_680111,Human_Splice_Rec_680121,Human_Splice_Rec_680129,Human_Splice_Rec_680135,Human_Splice_Rec_680141,Human_Splice_Rec_680145,Human_Splice_Rec_680153,Human_Splice_Rec_680163 RMVar_hsa_circ_94620,RMVar_hsa_circ_233706 77922 RMVar_ID_77922 Human_SNP_ID_246192716 m1A Human chr5 + 111757178 111757178 111757178 CCCGCTCCCTGTTCACTCTCTCTCCTCTCTACACCTGAAACACAAATGTGGTTGAAAAAGGGCAA CCCGCTCCCTGTTCACTCTCTCTCCTCTCTACCCCTGAAACACAAATGTGGTTGAAAAAGGGCAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:111757126..111757235;chr5:111757126..111757200 26863196 MeRIP-seq:(Medium) rs1230471363 Functional Loss SNV dbSNP153 33..33 33 - - - 77923 RMVar_ID_77923 Human_SNP_ID_246306460 m1A Human chr5 - 112161002 112161002 112161002 CGGCCCCGGACACTTCGGACACAGGCCGCCGCAGTCGACTCACCAGACTCAGGGTGGCCGCGTTC CGGCCCCGGACACTTCGGACACAGGCCGCCGCCGTCGACTCACCAGACTCAGGGTGGCCGCGTTC T G EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:112160901..112161027 26863410 MeRIP-seq:(Medium) rs1334967816 Functional Loss SNV dbSNP153 33..33 33 - - - 77924 RMVar_ID_77924 Human_SNP_ID_246307577 m1A Human chr5 - 112163996 112163996 112163996 CCTCTCCATAGATGACTTTGCAATCTACAGGGAAAATACTTATGCAGGACATCTTATATCTCCCC CCTCTCCATAGATGACTTTGCAATCTACAGGGCAAATACTTATGCAGGACATCTTATATCTCCCC T G EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:112163948..112164060 26863196 MeRIP-seq:(Medium) rs1406433021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233714,RMVar_hsa_circ_92988,RMVar_hsa_circ_83441,RMVar_hsa_circ_233713 77925 RMVar_ID_77925 Human_SNP_ID_246312975 m1A Human chr5 - 112183115 112183115 112183115 TTAAAAGAGATTAGGAAAGAACTCTGGAGTGTACCGGGGGGTTCACACCAGGACTCTTTTTACTG TTAAAAGAGATTAGGAAAGAACTCTGGAGTGTCCCGGGGGGTTCACACCAGGACTCTTTTTACTG T G EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112183110..112183310 26863196 MeRIP-seq:(Medium) rs1469055759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_628537 RMVar_hsa_circ_17593,RMVar_hsa_circ_233714,RMVar_hsa_circ_92988,RMVar_hsa_circ_83441,RMVar_hsa_circ_43976,RMVar_hsa_circ_267459,RMVar_hsa_circ_233713,RMVar_hsa_circ_325312,RMVar_hsa_circ_267117,RMVar_hsa_circ_40289,RMVar_hsa_circ_69643,RMVar_hsa_circ_233715,RMVar_hsa_circ_233716,RMVar_hsa_circ_74826 77926 RMVar_ID_77926 Human_SNP_ID_246313171 m1A Human chr5 - 112183980 112183980 112183980 TGTGGACTCTTTTTATACCTTGATTCAAAAACACTGAATTTGAAGTAGCATGTGGATATTCAGGT TGTGGACTCTTTTTATACCTTGATTCAAAAACGCTGAATTTGAAGTAGCATGTGGATATTCAGGT T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112183977..112184171 26863196 MeRIP-seq:(Medium) rs1467778738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24502798 RMVar_hsa_circ_17593,RMVar_hsa_circ_233714,RMVar_hsa_circ_92988,RMVar_hsa_circ_83441,RMVar_hsa_circ_43976,RMVar_hsa_circ_267459,RMVar_hsa_circ_233713,RMVar_hsa_circ_325312,RMVar_hsa_circ_267117,RMVar_hsa_circ_40289,RMVar_hsa_circ_69643,RMVar_hsa_circ_233715,RMVar_hsa_circ_233716,RMVar_hsa_circ_74826 77927 RMVar_ID_77927 Human_SNP_ID_246316445 m1A Human chr5 + 112196064 112196064 112196064 TGGATGCCCTTTCCCATACCCTGAGGCTCCAAATTCTCTTTATCTCTTCTCTCATAATCTCCTCC TGGATGCCCTTTCCCATACCCTGAGGCTCCAAGTTCTCTTTATCTCTTCTCTCATAATCTCCTCC A G AC010261.2 Ensembl:ENSG00000251187 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112196061..112196181 26863196 MeRIP-seq:(Medium) rs1235510734 Functional Loss SNV dbSNP153 33..33 33 - - - 77928 RMVar_ID_77928 Human_SNP_ID_246316663 m1A Human chr5 - 112197016 112197016 112197016 GAGGGACTAACCTTGGTAGTAAGGATAAATCCATAAATAACAGAGAGGAAGATGTTGGTAAGTTT GAGGGACTAACCTTGGTAGTAAGGATAAATCCGTAAATAACAGAGAGGAAGATGTTGGTAAGTTT T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112197014..112197098 26863196 MeRIP-seq:(Medium) rs1171178502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74579,RMVar_hsa_circ_17593,RMVar_hsa_circ_233714,RMVar_hsa_circ_83441,RMVar_hsa_circ_267117,RMVar_hsa_circ_40289,RMVar_hsa_circ_24050,RMVar_hsa_circ_233716,RMVar_hsa_circ_115628,RMVar_hsa_circ_368278,RMVar_hsa_circ_29003,RMVar_hsa_circ_233718,RMVar_hsa_circ_19607,RMVar_hsa_circ_233719,RMVar_hsa_circ_233717,RMVar_hsa_circ_52871 77929 RMVar_ID_77929 Human_SNP_ID_246358062 m1A Human chr5 - 112348147 112348147 112348147 GGCAGAGACTATAGAGTGAGGATAGGCAATTCAGGTGGAGGGAGTGACATAGAGAAAAGTGTAAT GGCAGAGACTATAGAGTGAGGATAGGCAATTCTGGTGGAGGGAGTGACATAGAGAAAAGTGTAAT T A EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112348127..112348192 26863196 MeRIP-seq:(Medium) rs1561593898 Functional Loss SNV dbSNP153 33..33 33 - - - 77930 RMVar_ID_77930 Human_SNP_ID_246363989 m1A Human chr5 - 112368885 112368885 112368885 CGAGAATTGGAGACAGAGGAGTGAGAAGGCAGAGTGAAAGACAAAGACTGTAACAAAAGATAGAA CGAGAATTGGAGACAGAGGAGTGAGAAGGCAGGGTGAAAGACAAAGACTGTAACAAAAGATAGAA T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:112368442..112369106 26863196 MeRIP-seq:(Medium) rs989998372 Functional Loss SNV dbSNP153 33..33 33 - - - 77931 RMVar_ID_77931 Human_SNP_ID_246378381 m1A Human chr5 - 112419614 112419610 112419615 CGGGGCGTCGTGGGTGCTCCTCACACAAAAGAAAAGCCGAGCGCTTCATACTCGGCGGATCTGAC CGGGGCGTCGTGGGTGCTCCTCACACAAAAG_____CCGAGCGCTTCATACTCGGCGGATCTGAC GCTTTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112419563..112420159 26863196 MeRIP-seq:(Medium) rs1274880810 Functional Loss DEL dbSNP153 32..36 33 - - - 77932 RMVar_ID_77932 Human_SNP_ID_246461870 m1A Human chr5 + 112707682 112707682 112707682 GTACTGTTGTTGGCTGTTGGTGAGGAAGGTGAAGCACTCAGTTGCCTTCTCGGGCCTCGGCGCCC GTACTGTTGTTGGCTGTTGGTGAGGAAGGTGATGCACTCAGTTGCCTTCTCGGGCCTCGGCGCCC A T APC Ensembl:ENSG00000134982 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:112707536..112707741 26863196 MeRIP-seq:(Medium) rs1331978936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2842844,Human_miRNA_ID_2931404 RMVar_hsa_circ_107256,RMVar_hsa_circ_233748 77933 RMVar_ID_77933 Human_SNP_ID_246507749 m1A Human chr5 - 112861350 112861350 112861350 AGCCATCTTCACAAGAGTCTCAACAACCCAGGAGCCGCAGGGAGAAACCCGGCAGAAACCCGGGA AGCCATCTTCACAAGAGTCTCAACAACCCAGGTGCCGCAGGGAGAAACCCGGCAGAAACCCGGGA T A RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:112861301..112861375 32194978 MeRIP-seq:(Medium) rs1193376070 Functional Loss SNV dbSNP153 33..33 33 - - - 77934 RMVar_ID_77934 Human_SNP_ID_246507765 m1A Human chr5 - 112861372 112861372 112861372 CCGGGGACCGCGCGGCAGCGCAAGCCATCTTCACAAGAGTCTCAACAACCCAGGAGCCGCAGGGA CCGGGGACCGCGCGGCAGCGCAAGCCATCTTCGCAAGAGTCTCAACAACCCAGGAGCCGCAGGGA T C RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:112861321..112862434 26863196 MeRIP-seq:(Medium) rs762085726 Functional Loss SNV dbSNP153 33..33 33 - - - 77935 RMVar_ID_77935 Human_SNP_ID_246515240 m1A Human chr5 - 112886976 112886974 112886977 CTCAGGAACAAGATGGCCCCACATGTGAGAGGAGATGTGACACACTGGGCTCAAATAACAGGCTT CTCAGGAACAAGATGGCCCCACATGTGAGAG___ATGTGACACACTGGGCTCAAATAACAGGCTT TCTC T REEP5 Ensembl:ENSG00000129625 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112886973..112887117 26863196 MeRIP-seq:(Medium) rs756668268 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_233794,RMVar_hsa_circ_104264 77936 RMVar_ID_77936 Human_SNP_ID_246516583 m1A Human chr5 + 112891920 112891917 112891920 GGAGCAGAAGGCACAAGAAGAATTCAGAATAAAGAAGGAAAAGGAAGAGGCGGCTAAAAAATGGC GGAGCAGAAGGCACAAGAAGAATTCAGAAT___GAAGGAAAAGGAAGAGGCGGCTAAAAAATGGC TAAA T ZRSR2P1,SRP19 Ensembl:ENSG00000212643,Ensembl:ENSG00000153037 Pseudogene,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112891913..112892012 26863196 MeRIP-seq:(Medium) rs1394112798 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_77401,Human_RBP_ID_5611809,Human_RBP_ID_18538590 RMVar_hsa_circ_233795,RMVar_hsa_circ_267187 77937 RMVar_ID_77937 Human_SNP_ID_246516584 m1A Human chr5 + 112891920 112891918 112891921 GGAGCAGAAGGCACAAGAAGAATTCAGAATAAAGAAGGAAAAGGAAGAGGCGGCTAAAAAATGGC GGAGCAGAAGGCACAAGAAGAATTCAGAATA___AAGGAAAAGGAAGAGGCGGCTAAAAAATGGC AAAG A ZRSR2P1,SRP19 Ensembl:ENSG00000212643,Ensembl:ENSG00000153037 Pseudogene,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112891913..112892012 26863196 MeRIP-seq:(Medium) rs1379914058 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_77401,Human_RBP_ID_5611809,Human_RBP_ID_18538590 RMVar_hsa_circ_233795,RMVar_hsa_circ_267187 77938 RMVar_ID_77938 Human_SNP_ID_246516626 m1A Human chr5 + 112892016 112892014 112892017 ATGGAAAGAACAGCAGAGGAAAGAGAGAGAAGAGGAGGAGCAGAAACAACAGGAGAAGAAAGAAA ATGGAAAGAACAGCAGAGGAAAGAGAGAGAA___GAGGAGCAGAAACAACAGGAGAAGAAAGAAA AGAG A ZRSR2P1,SRP19 Ensembl:ENSG00000212643,Ensembl:ENSG00000153037 Pseudogene,Protein coding exon,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:112891765..112892110 26863196 MeRIP-seq:(Medium) rs754358702 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_77402,Human_RBP_ID_2882095,Human_RBP_ID_5103341,Human_RBP_ID_18538592 RMVar_hsa_circ_233795,RMVar_hsa_circ_267187 77939 RMVar_ID_77939 Human_SNP_ID_246517010 m1A Human chr5 - 112892854 112892854 112892854 GTGCGTTTGTGAGATTTCTTCCCCCTATGACTACTCTTTTTTCTCTCGGATTCCCCATTTCTTTT GTGCGTTTGTGAGATTTCTTCCCCCTATGACTGCTCTTTTTTCTCTCGGATTCCCCATTTCTTTT T C REEP5 Ensembl:ENSG00000129625 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:112892830..112892986 26863196 MeRIP-seq:(Medium) rs780298365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233794,RMVar_hsa_circ_104264,RMVar_hsa_circ_344625 77940 RMVar_ID_77940 Human_SNP_ID_246524995 m1A Human chr5 - 112921213 112921213 112921213 CTGGTGGCCTTGTACCTGGTGTTCGGTTATGGAGCCTCTCTCCTCTGCAACCTGATAGGATTTGG CTGGTGGCCTTGTACCTGGTGTTCGGTTATGGTGCCTCTCTCCTCTGCAACCTGATAGGATTTGG T A REEP5 Ensembl:ENSG00000129625 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:112921151..112921275 32194978 MeRIP-seq:(Medium) rs566604759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75053,Human_RBP_ID_628742,Human_RBP_ID_787224,Human_RBP_ID_946758,Human_RBP_ID_1318591,Human_RBP_ID_1642942,Human_RBP_ID_1984387,Human_RBP_ID_3753637,Human_RBP_ID_4804063,Human_RBP_ID_7365557,Human_RBP_ID_8599517,Human_RBP_ID_9167528,Human_RBP_ID_9335676,Human_RBP_ID_9398052,Human_RBP_ID_18830000,Human_RBP_ID_19124596,Human_RBP_ID_22459200 Human_Splice_Rec_680876,Human_Splice_Rec_680877,Human_Splice_Rec_680883,Human_Splice_Rec_680892,Human_Splice_Rec_680893,Human_Splice_Rec_680898,Human_Splice_Rec_680899,Human_Splice_Rec_680908,Human_Splice_Rec_680909,Human_Splice_Rec_680915,Human_Splice_Rec_680920,Human_Splice_Rec_680921 Human_miRNA_ID_2136001,Human_miRNA_ID_2271857,Human_miRNA_ID_2369404,Human_miRNA_ID_2608669,Human_miRNA_ID_2664795,Human_miRNA_ID_2705686 RMVar_hsa_circ_233794,RMVar_hsa_circ_104264 77941 RMVar_ID_77941 Human_SNP_ID_246524996 m1A Human chr5 - 112921213 112921213 112921213 CTGGTGGCCTTGTACCTGGTGTTCGGTTATGGAGCCTCTCTCCTCTGCAACCTGATAGGATTTGG CTGGTGGCCTTGTACCTGGTGTTCGGTTATGGCGCCTCTCTCCTCTGCAACCTGATAGGATTTGG T G REEP5 Ensembl:ENSG00000129625 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:112921151..112921275 32194978 MeRIP-seq:(Medium) rs566604759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75053,Human_RBP_ID_628742,Human_RBP_ID_787224,Human_RBP_ID_946758,Human_RBP_ID_1318591,Human_RBP_ID_1642942,Human_RBP_ID_1984387,Human_RBP_ID_3753637,Human_RBP_ID_4804063,Human_RBP_ID_7365557,Human_RBP_ID_8599517,Human_RBP_ID_9167528,Human_RBP_ID_9335676,Human_RBP_ID_9398052,Human_RBP_ID_18830000,Human_RBP_ID_19124596,Human_RBP_ID_22459200 Human_Splice_Rec_680876,Human_Splice_Rec_680877,Human_Splice_Rec_680883,Human_Splice_Rec_680892,Human_Splice_Rec_680893,Human_Splice_Rec_680898,Human_Splice_Rec_680899,Human_Splice_Rec_680908,Human_Splice_Rec_680909,Human_Splice_Rec_680915,Human_Splice_Rec_680920,Human_Splice_Rec_680921 Human_miRNA_ID_2136001,Human_miRNA_ID_2271857,Human_miRNA_ID_2369404,Human_miRNA_ID_2608669,Human_miRNA_ID_2664795,Human_miRNA_ID_2705686 RMVar_hsa_circ_233794,RMVar_hsa_circ_104264 77942 RMVar_ID_77942 Human_SNP_ID_246525427 m1A Human chr5 + 112922177 112922177 112922177 TCTCGTGCAGGAACCGGTCGAACCTCTCCCTCATGGCCGCAGACATGGCGGGGACCGTCTCGCCG TCTCGTGCAGGAACCGGTCGAACCTCTCCCTCGTGGCCGCAGACATGGCGGGGACCGTCTCGCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:112922126..112922275;chr5:112922126..112922280;chr5:112922126..112922278 26863196 MeRIP-seq:(Medium) rs780984444 Functional Loss SNV dbSNP153 33..33 33 - - - 77943 RMVar_ID_77943 Human_SNP_ID_246525480 m1A Human chr5 - 112922239 112922239 112922239 GCCTGCCGCTGCTCCGCCGCAGTCGCCGCTCCAGTCTATCCGGCACTAGGAACAGCCCCGAGCGG GCCTGCCGCTGCTCCGCCGCAGTCGCCGCTCCGGTCTATCCGGCACTAGGAACAGCCCCGAGCGG T C REEP5 Ensembl:ENSG00000129625 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:112922151..112922286 26863410 MeRIP-seq:(Medium) rs1473358470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250722,Human_RBP_ID_628747,Human_RBP_ID_4845296,Human_RBP_ID_18424993 77944 RMVar_ID_77944 Human_SNP_ID_246541496 m1A Human chr5 + 112976855 112976851 112976855 CCGCGGCTTCCTCGGCTGCCAGCTCTCCGGCGAGCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC CCGCGGCTTCCTCGGCTGCCAGCTCTCCG____GCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC GGCGA G DCP2 Ensembl:ENSG00000172795 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112976806..112976951 26863196 MeRIP-seq:(Medium) rs1350858810 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4804084,Human_RBP_ID_9335283 RMVar_hsa_circ_100756,RMVar_hsa_circ_233797 77945 RMVar_ID_77945 Human_SNP_ID_246541503 m1A Human chr5 + 112976855 112976855 112976855 CCGCGGCTTCCTCGGCTGCCAGCTCTCCGGCGAGCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC CCGCGGCTTCCTCGGCTGCCAGCTCTCCGGCGGGCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC A G DCP2 Ensembl:ENSG00000172795 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112976806..112976951 26863196 MeRIP-seq:(Medium) rs181529366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4804084,Human_RBP_ID_9335283 RMVar_hsa_circ_100756,RMVar_hsa_circ_233797 77946 RMVar_ID_77946 Human_SNP_ID_246541504 m1A Human chr5 + 112976855 112976855 112976855 CCGCGGCTTCCTCGGCTGCCAGCTCTCCGGCGAGCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC CCGCGGCTTCCTCGGCTGCCAGCTCTCCGGCGTGCCGGAGTCCTAGTGCCGTACCGTCAGTCCCC A T DCP2 Ensembl:ENSG00000172795 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:112976806..112976951 26863196 MeRIP-seq:(Medium) rs181529366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4804084,Human_RBP_ID_9335283 RMVar_hsa_circ_100756,RMVar_hsa_circ_233797 77947 RMVar_ID_77947 Human_SNP_ID_246691450 m1A Human chr5 + 113514026 113514026 113514026 CAAGGGGCTGAAGGACATTCGCATTGATGAGGAGGTGAAGATCGCAGTCAATATCGCGCTGGAGC CAAGGGGCTGAAGGACATTCGCATTGATGAGGGGGTGAAGATCGCAGTCAATATCGCGCTGGAGC A G YTHDC2 Ensembl:ENSG00000047188 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:113513955..113514033 26863196 MeRIP-seq:(Medium) rs1372929745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1984531 Human_Splice_Rec_681163,Human_Splice_Rec_681193,Human_Splice_Rec_681251 77948 RMVar_ID_77948 Human_SNP_ID_247206251 m1A Human chr5 - 115262807 115262807 115262807 GAGGATGAGAGGCTAGCAGGGAGCGGTGAGGGAGAGCGGCTGGATTTCTTACGGGATCGGCACGT GAGGATGAGAGGCTAGCAGGGAGCGGTGAGGGCGAGCGGCTGGATTTCTTACGGGATCGGCACGT T G PGGT1B Ensembl:ENSG00000164219 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115262735..115262816 26863196 MeRIP-seq:(Medium) rs1320506231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845879 Human_Splice_Rec_681531,Human_Splice_Rec_681547,Human_Splice_Rec_681575 77949 RMVar_ID_77949 Human_SNP_ID_247214676 m1A Human chr5 + 115296511 115296511 115296511 CCTGCCACAGCCCCGGCTACCGCGGTGGCCGCAGCCGCTACCACAACCGTCGTCAGTGCGGCCAT CCTGCCACAGCCCCGGCTACCGCGGTGGCCGCGGCCGCTACCACAACCGTCGTCAGTGCGGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115296463..115296607 26863196 MeRIP-seq:(Medium) rs1239132080 Functional Loss SNV dbSNP153 33..33 33 - - - 77950 RMVar_ID_77950 Human_SNP_ID_247278739 m1A Human chr5 - 115538827 115538827 115538827 TGTGGATCTGTGGAAGGGTTTTGGCAGTTTTGAAGGTTTAGGAAATGGCATAAGGAAAGGCACTT TGTGGATCTGTGGAAGGGTTTTGGCAGTTTTGTAGGTTTAGGAAATGGCATAAGGAAAGGCACTT T A FEM1C Ensembl:ENSG00000145780 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115538810..115538952 26863196 MeRIP-seq:(Medium) rs1001498480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24077522 RMVar_hsa_circ_89354,RMVar_hsa_circ_233877,RMVar_hsa_circ_233882,RMVar_hsa_circ_233881 77951 RMVar_ID_77951 Human_SNP_ID_247278740 m1A Human chr5 - 115538827 115538827 115538827 TGTGGATCTGTGGAAGGGTTTTGGCAGTTTTGAAGGTTTAGGAAATGGCATAAGGAAAGGCACTT TGTGGATCTGTGGAAGGGTTTTGGCAGTTTTGGAGGTTTAGGAAATGGCATAAGGAAAGGCACTT T C FEM1C Ensembl:ENSG00000145780 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115538810..115538952 26863196 MeRIP-seq:(Medium) rs1001498480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24077522 RMVar_hsa_circ_89354,RMVar_hsa_circ_233877,RMVar_hsa_circ_233882,RMVar_hsa_circ_233881 77952 RMVar_ID_77952 Human_SNP_ID_247280236 m1A Human chr5 + 115544695 115544695 115544695 CCAAAGGAATGAATCCGGCCGCGCTGTTCGCCACGCCCCGCCACCCGAGCTGCCTCCCGCCCTTA CCAAAGGAATGAATCCGGCCGCGCTGTTCGCCCCGCCCCGCCACCCGAGCTGCCTCCCGCCCTTA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:115544357..115544753 26863196 MeRIP-seq:(Medium) rs900301697 Functional Loss SNV dbSNP153 33..33 33 - - - 77953 RMVar_ID_77953 Human_SNP_ID_247289863 m1A Human chr5 + 115581027 115581027 115581027 CTTCTGCATGCAATATCACAAATTTGAGGAACACCTCTTCTTCAGCTTCTTCTTCAAACATCTCT CTTCTGCATGCAATATCACAAATTTGAGGAACGCCTCTTCTTCAGCTTCTTCTTCAAACATCTCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:115580977..115581176 32194978 MeRIP-seq:(Medium) rs116674731 Functional Loss SNV dbSNP153 33..33 33 - - - 77954 RMVar_ID_77954 Human_SNP_ID_247295263 m1A Human chr5 + 115602265 115602265 115602265 CCAGTCCCCGCGACCACAGCAGCCTGCTCCCCACCGCGCTTGCAGAGCCCGGACGCGCGTGAGTC CCAGTCCCCGCGACCACAGCAGCCTGCTCCCCGCCGCGCTTGCAGAGCCCGGACGCGCGTGAGTC A G AC010226.1 Ensembl:ENSG00000249249 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115602219..115602436 26863196 MeRIP-seq:(Medium) rs1554093809 Functional Loss SNV dbSNP153 33..33 33 - - - 77955 RMVar_ID_77955 Human_SNP_ID_247300999 m1A Human chr5 - 115625724 115625724 115625724 GTCGCGGGCCGTTGGGGGTGCAGGCTGCTCGCACTGCTGCTACTGGTGCCTGGACCCGGCGGCGC GTCGCGGGCCGTTGGGGGTGCAGGCTGCTCGCCCTGCTGCTACTGGTGCCTGGACCCGGCGGCGC T G TMED7-TICAM2,TMED7 Ensembl:ENSG00000251201,Ensembl:ENSG00000134970 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:115625676..115626076 26863196 MeRIP-seq:(Medium) rs759763940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249699,Human_RBP_ID_629335,Human_RBP_ID_787288,Human_RBP_ID_4845300,Human_RBP_ID_5242402,Human_RBP_ID_9306564,Human_RBP_ID_17415287,Human_RBP_ID_18035991,Human_RBP_ID_18471927,Human_RBP_ID_22459202,Human_RBP_ID_27330377 Human_miRNA_ID_2098910,Human_miRNA_ID_2104859,Human_miRNA_ID_2110810,Human_miRNA_ID_2163356,Human_miRNA_ID_2594575,Human_miRNA_ID_2649437,Human_miRNA_ID_2651383,Human_miRNA_ID_2737522,Human_miRNA_ID_3038120 RMVar_hsa_circ_99654,RMVar_hsa_circ_233885 77956 RMVar_ID_77956 Human_SNP_ID_247361369 m1A Human chr5 - 115841511 115841511 115841511 GAGCCGCAGTCTGTGTTGCAGCTTCCTACTTCAATTGCTGCTGGAGGGGAAGGACTTACGGATGT GAGCCGCAGTCTGTGTTGCAGCTTCCTACTTCTATTGCTGCTGGAGGGGAAGGACTTACGGATGT T A ATG12 Ensembl:ENSG00000145782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115841433..115841514 26863196 MeRIP-seq:(Medium) rs750402145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1038270,Human_RBP_ID_1643232,Human_RBP_ID_4845883,Human_RBP_ID_9335678,Human_RBP_ID_9399295,Human_RBP_ID_18036047,Human_RBP_ID_22099540,Human_RBP_ID_22460130,Human_RBP_ID_26827315,Human_RBP_ID_27072837 77957 RMVar_ID_77957 Human_SNP_ID_247361370 m1A Human chr5 - 115841511 115841511 115841511 GAGCCGCAGTCTGTGTTGCAGCTTCCTACTTCAATTGCTGCTGGAGGGGAAGGACTTACGGATGT GAGCCGCAGTCTGTGTTGCAGCTTCCTACTTCCATTGCTGCTGGAGGGGAAGGACTTACGGATGT T G ATG12 Ensembl:ENSG00000145782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:115841433..115841514 26863196 MeRIP-seq:(Medium) rs750402145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1038270,Human_RBP_ID_1643232,Human_RBP_ID_4845883,Human_RBP_ID_9335678,Human_RBP_ID_9399295,Human_RBP_ID_18036047,Human_RBP_ID_22099540,Human_RBP_ID_22460130,Human_RBP_ID_26827315,Human_RBP_ID_27072837 77958 RMVar_ID_77958 Human_SNP_ID_247361758 m1A Human chr5 - 115842001 115842001 115842001 GTGCCGGGCCGACCGGGTGGGCACTGGGGGCCAGGGCGGGGGCGGGCGCGCGAGCCTCGCCTCGT GTGCCGGGCCGACCGGGTGGGCACTGGGGGCCGGGGCGGGGGCGGGCGCGCGAGCCTCGCCTCGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:115841954..115842068 26863196 MeRIP-seq:(Medium) rs1347363441 Functional Loss SNV dbSNP153 33..33 33 - - - 77959 RMVar_ID_77959 Human_SNP_ID_247361767 m1A Human chr5 - 115842011 115842011 115842011 GATCATGGCTGTGCCGGGCCGACCGGGTGGGCACTGGGGGCCAGGGCGGGGGCGGGCGCGCGAGC GATCATGGCTGTGCCGGGCCGACCGGGTGGGCGCTGGGGGCCAGGGCGGGGGCGGGCGCGCGAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:115841961..115842062 26863196 MeRIP-seq:(Medium) rs1459374832 Functional Loss SNV dbSNP153 33..33 33 - - - 77960 RMVar_ID_77960 Human_SNP_ID_247429634 m1A Human chr5 - 116083991 116083991 116083991 GGGCAGGTGGCAAATGCGGTGGGTCTGCAGAGATGTGGAGGGTGAGGCTGTGTGTTTCAGGTCAG GGGCAGGTGGCAAATGCGGTGGGTCTGCAGAGCTGTGGAGGGTGAGGCTGTGTGTTTCAGGTCAG T G AC034236.2 Ensembl:ENSG00000271918 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:116083940..116084102 26863196 MeRIP-seq:(Medium) rs1358200959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612290 77961 RMVar_ID_77961 Human_SNP_ID_247430146 m1A Human chr5 - 116085227 116085227 116085227 GCACTCCGCAGACGCAGCGTCGCAACCTCGGCAGCCCACCCCACCCCACCCCACTCAACCGGGCC GCACTCCGCAGACGCAGCGTCGCAACCTCGGCGGCCCACCCCACCCCACCCCACTCAACCGGGCC T C AC034236.2 Ensembl:ENSG00000271918 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:116085220..116085395 26863196 MeRIP-seq:(Medium) rs1364264483 Functional Loss SNV dbSNP153 33..33 33 - - - 77962 RMVar_ID_77962 Human_SNP_ID_248280953 m1A Human chr5 + 118988177 118988177 118988177 GGCATTTCCGAGATTTCCAACGTGCACCCGCCAACTCCGCCGCCCTAATCGCAGAGCTGCCCGAG GGCATTTCCGAGATTTCCAACGTGCACCCGCCGACTCCGCCGCCCTAATCGCAGAGCTGCCCGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:118988173..118988266 26863196 MeRIP-seq:(Medium) rs1188527682 Functional Loss SNV dbSNP153 33..33 33 - - - 77963 RMVar_ID_77963 Human_SNP_ID_248280954 m1A Human chr5 + 118988177 118988177 118988177 GGCATTTCCGAGATTTCCAACGTGCACCCGCCAACTCCGCCGCCCTAATCGCAGAGCTGCCCGAG GGCATTTCCGAGATTTCCAACGTGCACCCGCCTACTCCGCCGCCCTAATCGCAGAGCTGCCCGAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:118988173..118988266 26863196 MeRIP-seq:(Medium) rs1188527682 Functional Loss SNV dbSNP153 33..33 33 - - - 77964 RMVar_ID_77964 Human_SNP_ID_248281124 m1A Human chr5 - 118988404 118988404 118988404 CCGAACGACAAGGAGCGGCGGGAGGGCGGCGCAGTGCCGGCGGCGGCTGCCCTGGGCGCAGAGGC CCGAACGACAAGGAGCGGCGGGAGGGCGGCGCGGTGCCGGCGGCGGCTGCCCTGGGCGCAGAGGC T C DTWD2 Ensembl:ENSG00000169570 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:118988360..118988467;chr5:118988363..118988489 26863196 MeRIP-seq:(Medium) rs1031479863 Functional Loss SNV dbSNP153 33..33 33 - - - 77965 RMVar_ID_77965 Human_SNP_ID_248305140 m1A Human chr5 + 119071467 119071467 119071467 TCCAGGCGCCTGTCGCTGCTTCTGCCGTCGCCACCGAAGAGCGGCCGCCGCCCCTGAGGGAAGGA TCCAGGCGCCTGTCGCTGCTTCTGCCGTCGCCGCCGAAGAGCGGCCGCCGCCCCTGAGGGAAGGA A G DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:119071461..119071575 26863196 MeRIP-seq:(Medium) rs1171908544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845886,Human_RBP_ID_9335288 RMVar_hsa_circ_93745,RMVar_hsa_circ_233916 77966 RMVar_ID_77966 Human_SNP_ID_248319487 m1A Human chr5 + 119117610 119117610 119117610 AAGGGAGAGGTAGGGGACAGAAGGAGAGAGGTAGAAAGGGAAGGTGGCCTGGAAAGGCTGTGAAA AAGGGAGAGGTAGGGGACAGAAGGAGAGAGGTGGAAAGGGAAGGTGGCCTGGAAAGGCTGTGAAA A G DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:119117505..119117726 26863196 MeRIP-seq:(Medium) rs180711827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839712 RMVar_hsa_circ_87251,RMVar_hsa_circ_20836,RMVar_hsa_circ_93745,RMVar_hsa_circ_283706,RMVar_hsa_circ_233916,RMVar_hsa_circ_317746,RMVar_hsa_circ_29844,RMVar_hsa_circ_233921,RMVar_hsa_circ_233922,RMVar_hsa_circ_233923,RMVar_hsa_circ_315133,RMVar_hsa_circ_304728,RMVar_hsa_circ_111238,RMVar_hsa_circ_95111,RMVar_hsa_circ_30758,RMVar_hsa_circ_233925,RMVar_hsa_circ_233929,RMVar_hsa_circ_47155,RMVar_hsa_circ_233927,RMVar_hsa_circ_233928,RMVar_hsa_circ_233926,RMVar_hsa_circ_24610,RMVar_hsa_circ_330013,RMVar_hsa_circ_233924,RMVar_hsa_circ_280036,RMVar_hsa_circ_233936,RMVar_hsa_circ_233937,RMVar_hsa_circ_103706,RMVar_hsa_circ_313279,RMVar_hsa_circ_278253,RMVar_hsa_circ_87590,RMVar_hsa_circ_33027,RMVar_hsa_circ_233939,RMVar_hsa_circ_233941,RMVar_hsa_circ_233940,RMVar_hsa_circ_233938,RMVar_hsa_circ_96645,RMVar_hsa_circ_299599,RMVar_hsa_circ_233945,RMVar_hsa_circ_35326,RMVar_hsa_circ_59447,RMVar_hsa_circ_233946,RMVar_hsa_circ_233944,RMVar_hsa_circ_233947,RMVar_hsa_circ_342078 77967 RMVar_ID_77967 Human_SNP_ID_248364330 m1A Human chr5 + 119273426 119273426 119273426 TTTCCTTTAACAATGCCAGAGGAGCCCAGAGAATGGGGTGAATGTAGCACAACTTCAGTGATTGC TTTCCTTTAACAATGCCAGAGGAGCCCAGAGAGTGGGGTGAATGTAGCACAACTTCAGTGATTGC A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:119273421..119273610 26863196 MeRIP-seq:(Medium) rs1434778435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22613065 77968 RMVar_ID_77968 Human_SNP_ID_248375017 m1A Human chr5 + 119309507 119309507 119309507 TGTGGCTCGCTCCAGCACATTCTCCAAAAGGGATTCCCTTTCAACAGTTGTTTAAATAAGATGGC TGTGGCTCGCTCCAGCACATTCTCCAAAAGGGGTTCCCTTTCAACAGTTGTTTAAATAAGATGGC A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:119309503..119309687 26863196 MeRIP-seq:(Medium) rs1012909944 Functional Loss SNV dbSNP153 33..33 33 - - - 77969 RMVar_ID_77969 Human_SNP_ID_248379493 m1A Human chr5 - 119326722 119326722 119326722 TCATTTCCAGCCCCATCACCCCAACCTCCTTCAGGCTCATCCTCTGGCCTGAACTTCCTGTGCTT TCATTTCCAGCCCCATCACCCCAACCTCCTTCTGGCTCATCCTCTGGCCTGAACTTCCTGTGCTT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:119326715..119326864 26863196 MeRIP-seq:(Medium) rs1292558952 Functional Loss SNV dbSNP153 33..33 33 - - - 77970 RMVar_ID_77970 Human_SNP_ID_248389652 m1A Human chr5 + 119366173 119366173 119366173 CTAAAATGAAAAAAAAAAAAAGTAATATGTGCAAAACTTAAGAAGTGACCAGCAGTATAATAGGC CTAAAATGAAAAAAAAAAAAAGTAATATGTGCGAAACTTAAGAAGTGACCAGCAGTATAATAGGC A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:119365946..119366267 26863196 MeRIP-seq:(Medium) rs1320792848 Functional Loss SNV dbSNP153 33..33 33 - - - 77971 RMVar_ID_77971 Human_SNP_ID_248396872 m1A Human chr5 - 119392940 119392940 119392940 TGGGTGTACTCCCTGGTCACTCTGTAGAGCTCATCCAGCACCTCACTACTTGTGTCGTCTATTAA TGGGTGTACTCCCTGGTCACTCTGTAGAGCTCGTCCAGCACCTCACTACTTGTGTCGTCTATTAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:119392889..119392954 26863196 MeRIP-seq:(Medium) rs17849979 Functional Loss SNV dbSNP153 33..33 33 - - - 77972 RMVar_ID_77972 Human_SNP_ID_248413562 m1A Human chr5 - 119452635 119452629 119452635 CAAGGGGCGCGGCCTCCAACCTTCGCATGCTCACCTGCCCCCGCGCCGGTGACCAGTACCACCCG CAAGGGGCGCGGCCTCCAACCTTCGCATGCTC______CCCCGCGCCGGTGACCAGTACCACCCG GGCAGGT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr5:119452596..119452683;chr5:119452526..119452703 26863410 MeRIP-seq:(Medium) rs1554059509 Functional Loss DEL dbSNP153 33..38 33 - - - Clinvar_Rec_358 77973 RMVar_ID_77973 Human_SNP_ID_248416111 m1A Human chr5 + 119460857 119460857 119460857 GAACAGAAAATGCTTTAAGGAGAGACTGCAGGAAGTGAAGGAGTGCGCCTTGAGGAGATCTGCTG GAACAGAAAATGCTTTAAGGAGAGACTGCAGGTAGTGAAGGAGTGCGCCTTGAGGAGATCTGCTG A T HSD17B4 Ensembl:ENSG00000133835 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:119460854..119460919 26863196 MeRIP-seq:(Medium) rs998138312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7371361,Human_RBP_ID_15274261 RMVar_hsa_circ_354427,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,RMVar_hsa_circ_58193,RMVar_hsa_circ_58339 77974 RMVar_ID_77974 Human_SNP_ID_248419076 m1A Human chr5 + 119471687 119471687 119471687 AACCCTATGGAGAAGATCATTTCACAATGCAGATTCTTTGTTTCAAGTAATTCTCTTAAGTTCTG AACCCTATGGAGAAGATCATTTCACAATGCAGGTTCTTTGTTTCAAGTAATTCTCTTAAGTTCTG A G HSD17B4 Ensembl:ENSG00000133835 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:119471684..119474050 26863196 MeRIP-seq:(Medium) rs1366811402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25932842 Human_Splice_Rec_683134,Human_Splice_Rec_683135,Human_Splice_Rec_683276,Human_Splice_Rec_683277 RMVar_hsa_circ_354427,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,RMVar_hsa_circ_58193,RMVar_hsa_circ_58339,RMVar_hsa_circ_65791 77975 RMVar_ID_77975 Human_SNP_ID_248419773 m1A Human chr5 + 119473854 119473853 119473854 ATTAGAATTTCATTTTCCACACACACACACACACATTTTGAAAGTCTAGAATAATTAATTGTTGT ATTAGAATTTCATTTTCCACACACACACACAC_CATTTTGAAAGTCTAGAATAATTAATTGTTGT CA C HSD17B4 Ensembl:ENSG00000133835 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:119473851..119474063 26863196 MeRIP-seq:(Medium) rs869302843 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22553317 RMVar_hsa_circ_354427,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,RMVar_hsa_circ_58193,RMVar_hsa_circ_58339,RMVar_hsa_circ_65791 77976 RMVar_ID_77976 Human_SNP_ID_248419823 m1A Human chr5 + 119473985 119473985 119473985 TAGCTGCTGATAAGGTTGTTGAAGAAATAAGAAGGAGAGGTGGAAAAGCAGTGGCCAACTATGGT TAGCTGCTGATAAGGTTGTTGAAGAAATAAGAGGGAGAGGTGGAAAAGCAGTGGCCAACTATGGT A G HSD17B4 Ensembl:ENSG00000133835 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:119473841..119474053 26863196 MeRIP-seq:(Medium) rs1476913555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1985070,Human_RBP_ID_3967354,Human_RBP_ID_4848417,Human_RBP_ID_5610237,Human_RBP_ID_9398057,Human_RBP_ID_22460133,Human_RBP_ID_24078554,Human_RBP_ID_24548256,Human_RBP_ID_26350519 Human_Splice_Rec_682970,Human_Splice_Rec_682971,Human_Splice_Rec_682982,Human_Splice_Rec_682983,Human_Splice_Rec_682994,Human_Splice_Rec_682995,Human_Splice_Rec_683040,Human_Splice_Rec_683041,Human_Splice_Rec_683088,Human_Splice_Rec_683089,Human_Splice_Rec_683136,Human_Splice_Rec_683137,Human_Splice_Rec_683182,Human_Splice_Rec_683183,Human_Splice_Rec_683228,Human_Splice_Rec_683229,Human_Splice_Rec_683278,Human_Splice_Rec_683279,Human_Splice_Rec_683324,Human_Splice_Rec_683325,Human_Splice_Rec_683370,Human_Splice_Rec_683376,Human_Splice_Rec_683377,Human_Splice_Rec_683422,Human_Splice_Rec_683423,Human_Splice_Rec_683438,Human_Splice_Rec_683439,Human_Splice_Rec_683484,Human_Splice_Rec_683485,Human_Splice_Rec_683532,Human_Splice_Rec_683533,Human_Splice_Rec_683580,Human_Splice_Rec_683581,Human_Splice_Rec_683628,Human_Splice_Rec_683629,Human_Splice_Rec_683640,Human_Splice_Rec_683641 RMVar_hsa_circ_73028,RMVar_hsa_circ_354427,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,RMVar_hsa_circ_58193,RMVar_hsa_circ_58339,RMVar_hsa_circ_337737,RMVar_hsa_circ_363556,RMVar_hsa_circ_65791,RMVar_hsa_circ_358464,RMVar_hsa_circ_73519,RMVar_hsa_circ_36349,RMVar_hsa_circ_64069,RMVar_hsa_circ_233981 77977 RMVar_ID_77977 Human_SNP_ID_248419826 m1A Human chr5 + 119473988 119473988 119473988 CTGCTGATAAGGTTGTTGAAGAAATAAGAAGGAGAGGTGGAAAAGCAGTGGCCAACTATGGTATG CTGCTGATAAGGTTGTTGAAGAAATAAGAAGGTGAGGTGGAAAAGCAGTGGCCAACTATGGTATG A T HSD17B4 Ensembl:ENSG00000133835 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:119473850..119474072 26863196 MeRIP-seq:(Medium) rs760431947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1985070,Human_RBP_ID_3967354,Human_RBP_ID_9398057,Human_RBP_ID_22460133,Human_RBP_ID_24078554,Human_RBP_ID_24548256,Human_RBP_ID_26350519 Human_Splice_Rec_682970,Human_Splice_Rec_682971,Human_Splice_Rec_682982,Human_Splice_Rec_682983,Human_Splice_Rec_682994,Human_Splice_Rec_682995,Human_Splice_Rec_683040,Human_Splice_Rec_683041,Human_Splice_Rec_683088,Human_Splice_Rec_683089,Human_Splice_Rec_683136,Human_Splice_Rec_683137,Human_Splice_Rec_683182,Human_Splice_Rec_683183,Human_Splice_Rec_683228,Human_Splice_Rec_683229,Human_Splice_Rec_683278,Human_Splice_Rec_683279,Human_Splice_Rec_683324,Human_Splice_Rec_683325,Human_Splice_Rec_683370,Human_Splice_Rec_683376,Human_Splice_Rec_683377,Human_Splice_Rec_683422,Human_Splice_Rec_683423,Human_Splice_Rec_683438,Human_Splice_Rec_683439,Human_Splice_Rec_683484,Human_Splice_Rec_683485,Human_Splice_Rec_683532,Human_Splice_Rec_683533,Human_Splice_Rec_683580,Human_Splice_Rec_683581,Human_Splice_Rec_683628,Human_Splice_Rec_683629,Human_Splice_Rec_683640,Human_Splice_Rec_683641 RMVar_hsa_circ_73028,RMVar_hsa_circ_354427,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,RMVar_hsa_circ_58193,RMVar_hsa_circ_58339,RMVar_hsa_circ_337737,RMVar_hsa_circ_363556,RMVar_hsa_circ_65791,RMVar_hsa_circ_358464,RMVar_hsa_circ_73519,RMVar_hsa_circ_36349,RMVar_hsa_circ_64069,RMVar_hsa_circ_233981 77978 RMVar_ID_77978 Human_SNP_ID_248424677 m1A Human chr5 + 119492123 119492123 119492123 TTTTGGTAGGTTGGAGCAGGATGGATTGGAAAATGTAAGTCTCTCTCAGTTTTTGGTTTGTATAG TTTTGGTAGGTTGGAGCAGGATGGATTGGAAAGTGTAAGTCTCTCTCAGTTTTTGGTTTGTATAG A G HSD17B4 Ensembl:ENSG00000133835 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:119489248..119492164 32194978 MeRIP-seq:(Medium) rs1235458878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944452,Human_RBP_ID_5397368,Human_RBP_ID_9349663,Human_RBP_ID_19126084,Human_RBP_ID_22680619,Human_RBP_ID_25933299 Human_Splice_Rec_683008,Human_Splice_Rec_683009,Human_Splice_Rec_683054,Human_Splice_Rec_683055,Human_Splice_Rec_683102,Human_Splice_Rec_683103,Human_Splice_Rec_683150,Human_Splice_Rec_683151,Human_Splice_Rec_683196,Human_Splice_Rec_683197,Human_Splice_Rec_683242,Human_Splice_Rec_683292,Human_Splice_Rec_683293,Human_Splice_Rec_683340,Human_Splice_Rec_683390,Human_Splice_Rec_683391,Human_Splice_Rec_683452,Human_Splice_Rec_683453,Human_Splice_Rec_683500,Human_Splice_Rec_683501,Human_Splice_Rec_683548,Human_Splice_Rec_683549,Human_Splice_Rec_683594,Human_Splice_Rec_683595,Human_Splice_Rec_683662,Human_Splice_Rec_683663,Human_Splice_Rec_683698,Human_Splice_Rec_683699,Human_Splice_Rec_683742,Human_Splice_Rec_683743,Human_Splice_Rec_683778,Human_Splice_Rec_683779,Human_Splice_Rec_683812 RMVar_hsa_circ_87060,RMVar_hsa_circ_73028,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_363556,RMVar_hsa_circ_358464,RMVar_hsa_circ_73519,RMVar_hsa_circ_75092,RMVar_hsa_circ_36349,RMVar_hsa_circ_64069,RMVar_hsa_circ_233981,RMVar_hsa_circ_233982,RMVar_hsa_circ_96673,RMVar_hsa_circ_350563,RMVar_hsa_circ_361375,RMVar_hsa_circ_354271,RMVar_hsa_circ_272157,RMVar_hsa_circ_40470,RMVar_hsa_circ_58377,RMVar_hsa_circ_75060,RMVar_hsa_circ_53834,RMVar_hsa_circ_233983,RMVar_hsa_circ_17603 77979 RMVar_ID_77979 Human_SNP_ID_671102687 m1A Human chr20 - 297639 297639 297639 CGCCCCGGGCCGCGGGCCGCGCGGGGGGCAGAAGCTGCGGCCGCCCCCGTTTCCTCTCTTCCTCC CGCCCCGGGCCGCGGGCCGCGCGGGGGGCAGAGGCTGCGGCCGCCCCCGTTTCCTCTCTTCCTCC T C lnc-C20orf96-1 RNACentral:URS0000D573B0 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr20:297590..297975;chr20:297551..297843 26863196 MeRIP-seq:(Medium) rs111943584 Functional Loss SNV dbSNP153 33..33 33 - - - 77980 RMVar_ID_77980 Human_SNP_ID_671110567 m1A Human chr20 - 326451 326451 326451 ACAGCTCCCGCCCCGGGGTCTCGACCAGGCGCACTTCCAGCAGCTCCTCGTCGTCGTCTTCATCG ACAGCTCCCGCCCCGGGGTCTCGACCAGGCGCGCTTCCAGCAGCTCCTCGTCGTCGTCTTCATCG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:326426..326450 26863196 MeRIP-seq:(Medium) rs1165889458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8260609 77981 RMVar_ID_77981 Human_SNP_ID_671110588 m1A Human chr20 - 326493 326493 326493 CCGCTTGTCCCCGAGCGGCCCGTCCCGCCGGGACCATCCTCCACAGCTCCCGCCCCGGGGTCTCG CCGCTTGTCCCCGAGCGGCCCGTCCCGCCGGGGCCATCCTCCACAGCTCCCGCCCCGGGGTCTCG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:326389..326775 26863196 MeRIP-seq:(Medium) rs1314417108 Functional Loss SNV dbSNP153 33..33 33 - - - 77982 RMVar_ID_77982 Human_SNP_ID_671110598 m1A Human chr20 - 326512 326512 326512 GACGGCCCTTGGGCGCGCTCCGCTTGTCCCCGAGCGGCCCGTCCCGCCGGGACCATCCTCCACAG GACGGCCCTTGGGCGCGCTCCGCTTGTCCCCGGGCGGCCCGTCCCGCCGGGACCATCCTCCACAG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr20:326476..326759;chr20:326476..326575 26863196 MeRIP-seq:(Medium) rs113440192 Functional Loss SNV dbSNP153 33..33 33 - - - 77983 RMVar_ID_77983 Human_SNP_ID_671110656 m1A Human chr20 + 326607 326607 326607 CTCCCCGACACCGTCGGAGGACGAGGAGCCGGAGGAAGAGGAGGAGGAGGCGGCAGCGGCTGAGG CTCCCCGACACCGTCGGAGGACGAGGAGCCGGGGGAAGAGGAGGAGGAGGCGGCAGCGGCTGAGG A G SOX12 Ensembl:ENSG00000177732 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:326326..326750 26863196 MeRIP-seq:(Medium) rs1446707122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5528883,Human_RBP_ID_20681272,Human_RBP_ID_23005060,Human_RBP_ID_26492787 77984 RMVar_ID_77984 Human_SNP_ID_671110818 m1A Human chr20 - 326989 326989 326989 TCTGGATCTGAGGGGGGATGGGCACGTCCAGGAGGGGGCAGGCTGCGCGGGAGATGGGGTGCCAG TCTGGATCTGAGGGGGGATGGGCACGTCCAGGGGGGGGCAGGCTGCGCGGGAGATGGGGTGCCAG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:326938..327238 26863196 MeRIP-seq:(Medium) rs1374671218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3654067,Human_RBP_ID_5323113,Human_RBP_ID_8203661,Human_RBP_ID_21983430 77985 RMVar_ID_77985 Human_SNP_ID_671110833 m1A Human chr20 + 327021 327021 327021 TCCTGGACGTGCCCATCCCCCCTCAGATCCAGACATGCCCCTCCCCCGCAGACACACCCCAAGGC TCCTGGACGTGCCCATCCCCCCTCAGATCCAGTCATGCCCCTCCCCCGCAGACACACCCCAAGGC A T SOX12 Ensembl:ENSG00000177732 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:326920..327109 26863410 MeRIP-seq:(Medium) rs1409769105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3654551,Human_RBP_ID_5132035,Human_RBP_ID_17086547,Human_RBP_ID_18950112,Human_RBP_ID_27484230 Human_miRNA_ID_1547630 77986 RMVar_ID_77986 Human_SNP_ID_671111310 m1A Human chr20 + 328287 328284 328287 TCTGCCCCGCCCCGCCCCTCCGGCCTCCCCACACCCCCCTTGCCCTCACTACCTGTATCTCACCG TCTGCCCCGCCCCGCCCCTCCGGCCTCCCC___CCCCCCTTGCCCTCACTACCTGTATCTCACCG CACA C SOX12 Ensembl:ENSG00000177732 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:328236..328383 26863196 MeRIP-seq:(Medium) rs1489378118 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5132039,Human_RBP_ID_18950116,Human_RBP_ID_22078942,Human_RBP_ID_27295427 77987 RMVar_ID_77987 Human_SNP_ID_671111312 m1A Human chr20 + 328287 328287 328287 TCTGCCCCGCCCCGCCCCTCCGGCCTCCCCACACCCCCCTTGCCCTCACTACCTGTATCTCACCG TCTGCCCCGCCCCGCCCCTCCGGCCTCCCCACCCCCCCCTTGCCCTCACTACCTGTATCTCACCG A C SOX12 Ensembl:ENSG00000177732 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:328236..328383 26863196 MeRIP-seq:(Medium) rs1256885486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132039,Human_RBP_ID_18950116,Human_RBP_ID_22078942,Human_RBP_ID_27295427 77988 RMVar_ID_77988 Human_SNP_ID_671113523 m1A Human chr20 - 336294 336280 336295 AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAAAAGAAAGAAGAAGAAGAAGAAAGAAGAAGAGAAG AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAA_______________GAAGAAAGAAGAAGAGAAG CTTCTTCTTCTTTCTT C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:336124..336351 26863196 MeRIP-seq:(Medium) rs1369860430 Functional Loss DEL dbSNP153 32..46 33 - - - 77989 RMVar_ID_77989 Human_SNP_ID_671113527 m1A Human chr20 - 336294 336283 336295 AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAAAAGAAAGAAGAAGAAGAAGAAAGAAGAAGAGAAG AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAA____________GAAGAAGAAAGAAGAAGAGAAG CTTCTTCTTTCTT C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:336124..336351 26863196 MeRIP-seq:(Medium) rs1164818588 Functional Loss DEL dbSNP153 32..43 33 - - - 77990 RMVar_ID_77990 Human_SNP_ID_671113532 m1A Human chr20 - 336294 336289 336294 AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAAAAGAAAGAAGAAGAAGAAGAAAGAAGAAGAGAAG AGAAGAAGAAGAGGAAGAGGAAGAAGAAGAAA_____GAAGAAGAAGAAGAAAGAAGAAGAGAAG CTTTCT C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:336124..336351 26863196 MeRIP-seq:(Medium) rs1266338297 Functional Loss DEL dbSNP153 33..37 33 - - - 77991 RMVar_ID_77991 Human_SNP_ID_671117232 m1A Human chr20 + 349754 349754 349754 TCCTACCTGCACCTCTTCTATGAGGACTGTGCAGGCACTGCTCTCAGCGACGACCCTGAGGGACC TCCTACCTGCACCTCTTCTATGAGGACTGTGCGGGCACTGCTCTCAGCGACGACCCTGAGGGACC A G NRSN2 Ensembl:ENSG00000125841 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:349311..353555 32194978 MeRIP-seq:(Medium) rs1487680300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660039 Human_Splice_Rec_2052591,Human_Splice_Rec_2052603,Human_Splice_Rec_2052611,Human_Splice_Rec_2052621,Human_Splice_Rec_2052627,Human_Splice_Rec_2052635,Human_Splice_Rec_2052639,Human_Splice_Rec_2052641,Human_Splice_Rec_2052643 RMVar_hsa_circ_125751,RMVar_hsa_circ_208241 77992 RMVar_ID_77992 Human_SNP_ID_671118283 m1A Human chr20 + 353759 353759 353759 GCAGGGTCCCTTTAGAGCCCAACTCCAGGTCAAATCTGGAGCTCAAATCCCAGTGCTCCCTCCCC GCAGGGTCCCTTTAGAGCCCAACTCCAGGTCAGATCTGGAGCTCAAATCCCAGTGCTCCCTCCCC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs6115689 Functional Loss SNV dbSNP153 33..33 33 - - - 77993 RMVar_ID_77993 Human_SNP_ID_671118284 m1A Human chr20 + 353759 353759 353759 GCAGGGTCCCTTTAGAGCCCAACTCCAGGTCAAATCTGGAGCTCAAATCCCAGTGCTCCCTCCCC GCAGGGTCCCTTTAGAGCCCAACTCCAGGTCATATCTGGAGCTCAAATCCCAGTGCTCCCTCCCC A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs6115689 Functional Loss SNV dbSNP153 33..33 33 - - - 77994 RMVar_ID_77994 Human_SNP_ID_671125669 m1A Human chr20 - 381364 381364 381364 GTCACCTGAAGCCCGGGGGGAGCACTCAGCCCAGGCCCGGATCAAAAGGGATCTGACCTGGCCGC GTCACCTGAAGCCCGGGGGGAGCACTCAGCCCGGGCCCGGATCAAAAGGGATCTGACCTGGCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:381361..381533 26863196 MeRIP-seq:(Medium) rs1490494733 Functional Loss SNV dbSNP153 33..33 33 - - - 77995 RMVar_ID_77995 Human_SNP_ID_671127612 m1A Human chr20 + 387968 387968 387968 TATCCTCCCACCAGCAGGGGAAAGGAGGGGCCACCAAGCAGTCTCACTTTAGTGCTTTTCTCTCC TATCCTCCCACCAGCAGGGGAAAGGAGGGGCCGCCAAGCAGTCTCACTTTAGTGCTTTTCTCTCC A G TRIB3 Ensembl:ENSG00000101255 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:387966..388157 26863196 MeRIP-seq:(Medium) rs571590335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79100,RMVar_hsa_circ_208243 77996 RMVar_ID_77996 Human_SNP_ID_671127677 m1A Human chr20 - 388115 388115 388115 CAGGGGGGCAGTCTGGGCTGGGGCCCACTTCGAGCTCGTTTCTGGACGGGACGCTCGGTATCTAA CAGGGGGGCAGTCTGGGCTGGGGCCCACTTCGGGCTCGTTTCTGGACGGGACGCTCGGTATCTAA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:387961..388171 26863196 MeRIP-seq:(Medium) rs753310737 Functional Loss SNV dbSNP153 33..33 33 - - - 77997 RMVar_ID_77997 Human_SNP_ID_671127788 m1A Human chr20 - 388303 388303 388303 TGGTGCTGGGGGACAGCCGCCCATGGGCACGTACCTTGCAGGTATACTCAGTGCCTGTAGGGCAG TGGTGCTGGGGGACAGCCGCCCATGGGCACGTGCCTTGCAGGTATACTCAGTGCCTGTAGGGCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:388263..391548 32194978 MeRIP-seq:(Medium) rs776619450 Functional Loss SNV dbSNP153 33..33 33 - - - 77998 RMVar_ID_77998 Human_SNP_ID_671133399 m1A Human chr20 - 408184 408184 408184 CCGGCGGCGGCGGACGCCGAGTGCGGGGTCCCAGCGGTCCCGGCGCTCCTGTTTGGGGCGACCCC CCGGCGGCGGCGGACGCCGAGTGCGGGGTCCCCGCGGTCCCGGCGCTCCTGTTTGGGGCGACCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:408138..408237 26863196 MeRIP-seq:(Medium) rs1188329671 Functional Loss SNV dbSNP153 33..33 33 - - - 77999 RMVar_ID_77999 Human_SNP_ID_671133469 m1A Human chr20 - 408371 408371 408371 GGAGCGCCCCTGGCGTCCCGGGTTTCAAGGCAAAGCCCTCTCTCCTCCCGGGAGGCCCCAGTTCT GGAGCGCCCCTGGCGTCCCGGGTTTCAAGGCAGAGCCCTCTCTCCTCCCGGGAGGCCCCAGTTCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:408301..408675 26863196 MeRIP-seq:(Medium) rs1311977074 Functional Loss SNV dbSNP153 33..33 33 - - - 78000 RMVar_ID_78000 Human_SNP_ID_671133483 m1A Human chr20 + 408408 408408 408408 TTGAAACCCGGGACGCCAGGGGCGCTCCCGCAAGTGGGGGTCCTCCGGGACTTGGAACGCCCCGG TTGAAACCCGGGACGCCAGGGGCGCTCCCGCACGTGGGGGTCCTCCGGGACTTGGAACGCCCCGG A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1187367739 Functional Loss SNV dbSNP153 33..33 33 - - - 78001 RMVar_ID_78001 Human_SNP_ID_671133914 m1A Human chr20 + 410016 410016 410016 TGTGCAACTGAAGCCTGAGGTCTCCCCAACGCAGGACATCAGGTGAGGAGTGCATGGCTGGCCTG TGTGCAACTGAAGCCTGAGGTCTCCCCAACGCCGGACATCAGGTGAGGAGTGCATGGCTGGCCTG A C RBCK1 Ensembl:ENSG00000125826 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:409918..410454 26863410 MeRIP-seq:(Medium) rs1263526700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925098,Human_RBP_ID_9331393,Human_RBP_ID_14107249,Human_RBP_ID_19003637 Human_Splice_Rec_2052679,Human_Splice_Rec_2052687,Human_Splice_Rec_2052709,Human_Splice_Rec_2052729,Human_Splice_Rec_2052749,Human_Splice_Rec_2052753,Human_Splice_Rec_2052779,Human_Splice_Rec_2052801,Human_Splice_Rec_2052823 RMVar_hsa_circ_107989,RMVar_hsa_circ_112454,RMVar_hsa_circ_208248,RMVar_hsa_circ_208249 78002 RMVar_ID_78002 Human_SNP_ID_671153712 m1A Human chr20 + 483377 483377 483377 ACATCTTGATGTAACTAAGACACACTTCCACAAGAGCCACTAGGATAACCCCACTGAAGCGCTTA ACATCTTGATGTAACTAAGACACACTTCCACAGGAGCCACTAGGATAACCCCACTGAAGCGCTTA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:483276..483600 32194978 MeRIP-seq:(Medium) rs963834908 Functional Loss SNV dbSNP153 33..33 33 - - - 78003 RMVar_ID_78003 Human_SNP_ID_671196776 m1A Human chr20 - 647962 647960 647962 GCACCTCTAGCTGCAAACAAAGCTAAGACAGCAGGGAACAGAATTGTCATGGCTGAATAGACCAA GCACCTCTAGCTGCAAACAAAGCTAAGACAGC__GGAACAGAATTGTCATGGCTGAATAGACCAA CCT C SRXN1,AL121758.1 Ensembl:ENSG00000271303,Ensembl:ENSG00000270299 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:647913..648251 26863196 MeRIP-seq:(Medium) rs764744943 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1094335,Human_miRNA_ID_1094336 78004 RMVar_ID_78004 Human_SNP_ID_671196777 m1A Human chr20 - 647962 647962 647962 GCACCTCTAGCTGCAAACAAAGCTAAGACAGCAGGGAACAGAATTGTCATGGCTGAATAGACCAA GCACCTCTAGCTGCAAACAAAGCTAAGACAGCTGGGAACAGAATTGTCATGGCTGAATAGACCAA T A SRXN1,AL121758.1 Ensembl:ENSG00000271303,Ensembl:ENSG00000270299 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:647913..648251 26863196 MeRIP-seq:(Medium) rs1347026928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1094335,Human_miRNA_ID_1094336 78005 RMVar_ID_78005 Human_SNP_ID_671196888 m1A Human chr20 - 648246 648246 648246 GTGGCTAATGGTATTGGTTCAACAACTCCACGAAGGTAGGGGTCACGTCTTGGATCCTTTTGCCT GTGGCTAATGGTATTGGTTCAACAACTCCACGGAGGTAGGGGTCACGTCTTGGATCCTTTTGCCT T C SRXN1,AL121758.1 Ensembl:ENSG00000271303,Ensembl:ENSG00000270299 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6053666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4658866,Human_RBP_ID_17975985,Human_RBP_ID_22081227 GWAS_ID_9311,GWAS_ID_9312,GWAS_ID_9313,GWAS_ID_9314,GWAS_ID_9315 78006 RMVar_ID_78006 Human_SNP_ID_671198233 m1A Human chr20 + 653160 653160 653160 CGGGCGCCCCCCGACCCGCGCCGGCCCTGCCCAGCGTTCCTCCTGCACGCAGCCCCATCGTCGCC CGGGCGCCCCCCGACCCGCGCCGGCCCTGCCCGGCGTTCCTCCTGCACGCAGCCCCATCGTCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:652922..653415 26863196 MeRIP-seq:(Medium) rs1364081706 Functional Loss SNV dbSNP153 33..33 33 - - - 78007 RMVar_ID_78007 Human_SNP_ID_671198236 m1A Human chr20 - 653165 653165 653165 GCGGCGGCGACGATGGGGCTGCGTGCAGGAGGAACGCTGGGCAGGGCCGGCGCGGGTCGGGGGGC GCGGCGGCGACGATGGGGCTGCGTGCAGGAGGGACGCTGGGCAGGGCCGGCGCGGGTCGGGGGGC T C SRXN1,AL121758.1 Ensembl:ENSG00000271303,Ensembl:ENSG00000270299 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:652976..653397 26863196 MeRIP-seq:(Medium) rs1299240565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660056,Human_RBP_ID_22453237 78008 RMVar_ID_78008 Human_SNP_ID_671245392 m1A Human chr20 - 833947 833947 833947 TCGCACCCGGACCCACCCGCGCCCTCACCTGGAGCCCGCGCTAGGCGTGTCCCGGCTCCTCTCGC TCGCACCCGGACCCACCCGCGCCCTCACCTGGCGCCCGCGCTAGGCGTGTCCCGGCTCCTCTCGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:833763..836078 32194978 MeRIP-seq:(Medium) rs537811205 Functional Loss SNV dbSNP153 33..33 33 - - - 78009 RMVar_ID_78009 Human_SNP_ID_671315323 m1A Human chr20 + 1118663 1118663 1118663 GTCTCCATTTTGGTCTCAGGTGTGGACTCGGCAAGAACCAGCGCAAGAGGGAAGCAGAGTTATAG GTCTCCATTTTGGTCTCAGGTGTGGACTCGGCCAGAACCAGCGCAAGAGGGAAGCAGAGTTATAG A C PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:1118601..1118832 26863196 MeRIP-seq:(Medium) rs938738293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1593038,Human_RBP_ID_1925913,Human_RBP_ID_3642783,Human_RBP_ID_4635931,Human_RBP_ID_5423961,Human_RBP_ID_5445371,Human_RBP_ID_5471633,Human_RBP_ID_5503748,Human_RBP_ID_8528143,Human_RBP_ID_8852685,Human_RBP_ID_9115071,Human_RBP_ID_18443977,Human_RBP_ID_18768453,Human_RBP_ID_22452677,Human_RBP_ID_26343912 RMVar_hsa_circ_208281,RMVar_hsa_circ_116860 78010 RMVar_ID_78010 Human_SNP_ID_671327047 m1A Human chr20 + 1166137 1166137 1166137 CAGACAGAGCACAGGAGCATGGGCTGCCTCTGAGTGTGGTGTTGAACTTCGGGAGGAGCAGGGAG CAGACAGAGCACAGGAGCATGGGCTGCCTCTGGGTGTGGTGTTGAACTTCGGGAGGAGCAGGGAG A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:1166058..1166209 32194978 MeRIP-seq:(Medium) rs1358083663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4635994,Human_RBP_ID_6977984,Human_RBP_ID_23893624 RMVar_hsa_circ_55856 78011 RMVar_ID_78011 Human_SNP_ID_671330492 m1A Human chr20 - 1181199 1181199 1181199 CTGGTGAGTGGGATTCTTCTGGTGGTGACAGCATACGCCATCCCCCGTGAGGCTCGAGTCAATCC CTGGTGAGTGGGATTCTTCTGGTGGTGACAGCGTACGCCATCCCCCGTGAGGCTCGAGTCAATCC T C TMEM74B Ensembl:ENSG00000125895 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:1181149..1181445 32194978 MeRIP-seq:(Medium) rs758564194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18167470,Human_RBP_ID_22080473 78012 RMVar_ID_78012 Human_SNP_ID_671366844 m1A Human chr20 + 1331174 1331174 1331174 CAGCACTCCCCCAGCACCTCTGCCTCAGCTGGACTGGGAGCCCCACCATTCCTGCCCCACTGCAC CAGCACTCCCCCAGCACCTCTGCCTCAGCTGGCCTGGGAGCCCCACCATTCCTGCCCCACTGCAC A C SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:1331146..1331328 26863196 MeRIP-seq:(Medium) rs1238299120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17085840,Human_RBP_ID_18951105 78013 RMVar_ID_78013 Human_SNP_ID_671376063 m1A Human chr20 + 1369619 1369619 1369619 CTCTCAACTTGGAGAGTAATTCAGTCCTCAACAGCGCCTCAAATCTGCTATGGCTTTGCAGCGCA CTCTCAACTTGGAGAGTAATTCAGTCCTCAACGGCGCCTCAAATCTGCTATGGCTTTGCAGCGCA A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:1369571..1369672 32194978 MeRIP-seq:(Medium) rs1346223535 Functional Loss SNV dbSNP153 33..33 33 - - - 78014 RMVar_ID_78014 Human_SNP_ID_671376221 m1A Human chr20 + 1370031 1370030 1370032 GTGGAACATCAGGAAAAGCTCCATATGGATTCATGTGCACATGTCTGGAGGCACCAGATCCCTCC GTGGAACATCAGGAAAAGCTCCATATGGATTC__GTGCACATGTCTGGAGGCACCAGATCCCTCC CAT C SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:1369720..1370075 32194978 MeRIP-seq:(Medium) rs755407950 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_150630 78015 RMVar_ID_78015 Human_SNP_ID_671376222 m1A Human chr20 + 1370031 1370031 1370031 GTGGAACATCAGGAAAAGCTCCATATGGATTCATGTGCACATGTCTGGAGGCACCAGATCCCTCC GTGGAACATCAGGAAAAGCTCCATATGGATTCCTGTGCACATGTCTGGAGGCACCAGATCCCTCC A C SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:1369720..1370075 32194978 MeRIP-seq:(Medium) rs1375526444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150630 78016 RMVar_ID_78016 Human_SNP_ID_671376223 m1A Human chr20 + 1370031 1370031 1370031 GTGGAACATCAGGAAAAGCTCCATATGGATTCATGTGCACATGTCTGGAGGCACCAGATCCCTCC GTGGAACATCAGGAAAAGCTCCATATGGATTCGTGTGCACATGTCTGGAGGCACCAGATCCCTCC A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:1369720..1370075 32194978 MeRIP-seq:(Medium) rs1375526444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150630 78017 RMVar_ID_78017 Human_SNP_ID_671381441 m1A Human chr20 - 1392883 1392883 1392883 CATCGGCTCAGCATGCCCGTCTCTGTCTCCTCAGGGCGCACCTTCCCCAAGCGCGGCCAGACCTG CATCGGCTCAGCATGCCCGTCTCTGTCTCCTCGGGGCGCACCTTCCCCAAGCGCGGCCAGACCTG T C AL136531.2,FKBP1A Ensembl:ENSG00000274322,Ensembl:ENSG00000088832 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:1378165..1393023 32194978 MeRIP-seq:(Medium) rs1387863510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559397,Human_RBP_ID_4659606,Human_RBP_ID_5384394,Human_RBP_ID_9331401,Human_RBP_ID_22670633,Human_RBP_ID_26787658,Human_RBP_ID_27294208 Human_Splice_Rec_2054079,Human_Splice_Rec_2054087,Human_Splice_Rec_2054139,Human_Splice_Rec_2054147,Human_Splice_Rec_2054157,Human_Splice_Rec_2054177,Human_Splice_Rec_2054181,Human_Splice_Rec_2054187,Human_Splice_Rec_2054195 RMVar_hsa_circ_87746,RMVar_hsa_circ_208288 78018 RMVar_ID_78018 Human_SNP_ID_671381490 m1A Human chr20 + 1393010 1393010 1393010 GGTTTCCACCTGCACTCCCATGGCGGCGGCGGACGCTGAGCGGGCGGGCGGCGCGACGGGCGGCG GGTTTCCACCTGCACTCCCATGGCGGCGGCGGTCGCTGAGCGGGCGGGCGGCGCGACGGGCGGCG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:1392895..1393075 26863196 MeRIP-seq:(Medium) rs1205726136 Functional Loss SNV dbSNP153 33..33 33 - - - 78019 RMVar_ID_78019 Human_SNP_ID_671381510 m1A Human chr20 - 1393043 1393031 1393043 CCGTGGAACCGCCGCCAGGTCGCTGTTGGTCCACGCCGCCCGTCGCGCCGCCCGCCCGCTCAGCG CCGTGGAACCGCCGCCAGGTCGCTGTTGGTCC____________GCGCCGCCCGCCCGCTCAGCG CGACGGGCGGCGT C AL136531.2,FKBP1A Ensembl:ENSG00000274322,Ensembl:ENSG00000088832 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:1392921..1393052 26863410 MeRIP-seq:(Medium) rs1317090043 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_559400,Human_RBP_ID_778579,Human_RBP_ID_926574,Human_RBP_ID_4636316,Human_RBP_ID_9331402,Human_RBP_ID_14037599,Human_RBP_ID_22452682,Human_RBP_ID_22533636 Human_Splice_Rec_2054077,Human_Splice_Rec_2054085,Human_Splice_Rec_2054137,Human_Splice_Rec_2054145,Human_Splice_Rec_2054151,Human_Splice_Rec_2054175,Human_Splice_Rec_2054185,Human_Splice_Rec_2054193 RMVar_hsa_circ_87746,RMVar_hsa_circ_208288 78020 RMVar_ID_78020 Human_SNP_ID_671381532 m1A Human chr20 + 1393056 1393056 1393056 GGCGGCGCGACGGGCGGCGTGGACCAACAGCGACCTGGCGGCGGTTCCACGGCTCTGCCTAGTAC GGCGGCGCGACGGGCGGCGTGGACCAACAGCGCCCTGGCGGCGGTTCCACGGCTCTGCCTAGTAC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:1392892..1393063 26863410 MeRIP-seq:(Medium) rs1457236550 Functional Loss SNV dbSNP153 33..33 33 - - - 78021 RMVar_ID_78021 Human_SNP_ID_671393343 m1A Human chr20 + 1443675 1443675 1443675 ACTGGACTGCTGGGTGTGCACAAGGGGGCAGGAGGGGCGATCCCCATGGGGCATGGCCACTGGCC ACTGGACTGCTGGGTGTGCACAAGGGGGCAGGCGGGGCGATCCCCATGGGGCATGGCCACTGGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:1443627..1443850 26863196 MeRIP-seq:(Medium) rs142406814 Functional Loss SNV dbSNP153 33..33 33 - - - 78022 RMVar_ID_78022 Human_SNP_ID_671393886 m1A Human chr20 - 1445776 1445776 1445776 ACCAGCTCTCCAGCCCAACAGGCAGAAAATGAAGCCAAAGCCAGCTCTTCCATCTTAATCGACGA ACCAGCTCTCCAGCCCAACAGGCAGAAAATGAGGCCAAAGCCAGCTCTTCCATCTTAATCGACGA T C NSFL1C Ensembl:ENSG00000088833 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:1445726..1445800 26863196 MeRIP-seq:(Medium) rs1202847985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1926198,Human_RBP_ID_22670634 Human_Splice_Rec_2054206,Human_Splice_Rec_2054220,Human_Splice_Rec_2054234,Human_Splice_Rec_2054252,Human_Splice_Rec_2054268,Human_Splice_Rec_2054298 Human_miRNA_ID_336951,Human_miRNA_ID_794633 RMVar_hsa_circ_49411,RMVar_hsa_circ_348298 78023 RMVar_ID_78023 Human_SNP_ID_671396903 m1A Human chr20 - 1458265 1458265 1458265 TTTGCTCCTTTCTGTGTCTCCAGTGATAATAGAGTGACATCCTTCAGAGACCTCATTCATGACCA TTTGCTCCTTTCTGTGTCTCCAGTGATAATAGGGTGACATCCTTCAGAGACCTCATTCATGACCA T C NSFL1C Ensembl:ENSG00000088833 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:1458173..1458273 32194978 MeRIP-seq:(Medium) rs139550416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559463,Human_RBP_ID_8528679,Human_RBP_ID_9347943,Human_RBP_ID_22670637,Human_RBP_ID_23894903 Human_Splice_Rec_2054212,Human_Splice_Rec_2054213,Human_Splice_Rec_2054224,Human_Splice_Rec_2054225,Human_Splice_Rec_2054240,Human_Splice_Rec_2054241,Human_Splice_Rec_2054258,Human_Splice_Rec_2054259,Human_Splice_Rec_2054274,Human_Splice_Rec_2054275,Human_Splice_Rec_2054288,Human_Splice_Rec_2054289,Human_Splice_Rec_2054304,Human_Splice_Rec_2054305,Human_Splice_Rec_2054318,Human_Splice_Rec_2054319,Human_Splice_Rec_2054328,Human_Splice_Rec_2054329,Human_Splice_Rec_2054336,Human_Splice_Rec_2054340 RMVar_hsa_circ_49411,RMVar_hsa_circ_74458,RMVar_hsa_circ_357584,RMVar_hsa_circ_299699,RMVar_hsa_circ_208291,RMVar_hsa_circ_208290 78024 RMVar_ID_78024 Human_SNP_ID_671396908 m1A Human chr20 - 1458272 1458272 1458272 AGATCATTTTGCTCCTTTCTGTGTCTCCAGTGATAATAGAGTGACATCCTTCAGAGACCTCATTC AGATCATTTTGCTCCTTTCTGTGTCTCCAGTGGTAATAGAGTGACATCCTTCAGAGACCTCATTC T C NSFL1C Ensembl:ENSG00000088833 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:1458148..1463383 26863196 MeRIP-seq:(Medium) rs376293006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8528679,Human_RBP_ID_9347943,Human_RBP_ID_22670637,Human_RBP_ID_23894903 Human_Splice_Rec_2054212,Human_Splice_Rec_2054213,Human_Splice_Rec_2054224,Human_Splice_Rec_2054225,Human_Splice_Rec_2054240,Human_Splice_Rec_2054241,Human_Splice_Rec_2054258,Human_Splice_Rec_2054259,Human_Splice_Rec_2054274,Human_Splice_Rec_2054275,Human_Splice_Rec_2054288,Human_Splice_Rec_2054289,Human_Splice_Rec_2054304,Human_Splice_Rec_2054305,Human_Splice_Rec_2054318,Human_Splice_Rec_2054319,Human_Splice_Rec_2054328,Human_Splice_Rec_2054329,Human_Splice_Rec_2054336,Human_Splice_Rec_2054340 RMVar_hsa_circ_49411,RMVar_hsa_circ_74458,RMVar_hsa_circ_357584,RMVar_hsa_circ_299699,RMVar_hsa_circ_208291,RMVar_hsa_circ_208290 78025 RMVar_ID_78025 Human_SNP_ID_671399050 m1A Human chr20 + 1466791 1466791 1466791 CCGGTCCTCCTCGGCGCCCGTCACCGCCACGAACTCCCTCAGCGCCTCCTGTCGCTCCGCCGCCA CCGGTCCTCCTCGGCGCCCGTCACCGCCACGATCTCCCTCAGCGCCTCCTGTCGCTCCGCCGCCA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:1466688..1466850 26863196 MeRIP-seq:(Medium) rs1212797015 Functional Loss SNV dbSNP153 33..33 33 - - - 78026 RMVar_ID_78026 Human_SNP_ID_671399066 m1A Human chr20 - 1466808 1466808 1466808 GGCGCACGGGGCGAAGATGGCGGCGGAGCGACAGGAGGCGCTGAGGGAGTTCGTGGCGGTGACGG GGCGCACGGGGCGAAGATGGCGGCGGAGCGACGGGAGGCGCTGAGGGAGTTCGTGGCGGTGACGG T C NSFL1C Ensembl:ENSG00000088833 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:1466627..1466850 26863196 MeRIP-seq:(Medium) rs1434858162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244704,Human_RBP_ID_831299,Human_RBP_ID_4636435,Human_RBP_ID_26342617,Human_RBP_ID_27819514 Human_Splice_Rec_2054209,Human_Splice_Rec_2054223,Human_Splice_Rec_2054237,Human_Splice_Rec_2054255,Human_Splice_Rec_2054271,Human_Splice_Rec_2054287,Human_Splice_Rec_2054299,Human_Splice_Rec_2054325,Human_Splice_Rec_2054335,Human_Splice_Rec_2054337,Human_Splice_Rec_2054341 78027 RMVar_ID_78027 Human_SNP_ID_671499583 m1A Human chr20 + 1893919 1893919 1893919 GGGCCTCCCACCCGCCCAGTCCGCCCTCCACCACCGAGACACCTGGCCAGGGGGCCTCCACCTCC GGGCCTCCCACCCGCCCAGTCCGCCCTCCACCGCCGAGACACCTGGCCAGGGGGCCTCCACCTCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:1893839..1893952 26863196 MeRIP-seq:(Medium) rs1178172804 Functional Loss SNV dbSNP153 33..33 33 - - - 78028 RMVar_ID_78028 Human_SNP_ID_671553369 m1A Human chr20 + 2102932 2102932 2102932 AGAGGTACACAAAGCCCGGAGCGGAAAAGGCGAAGCCCAGTGCCGCGGGCGCCCAGCACGAAGCT AGAGGTACACAAAGCCCGGAGCGGAAAAGGCGGAGCCCAGTGCCGCGGGCGCCCAGCACGAAGCT A G STK35 Ensembl:ENSG00000125834 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:2101874..2103264;chr20:2101845..2103296 26863196 MeRIP-seq:(Medium) rs1203017171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4637714 RMVar_hsa_circ_115283,RMVar_hsa_circ_208298 78029 RMVar_ID_78029 Human_SNP_ID_671553436 m1A Human chr20 + 2103040 2103040 2103040 GAGGCCCCGGGCGAGGCCTTCCTGGCGCGGCGACGGCCTGAGGGCGGTGGCGGGTCCGCGCGGCC GAGGCCCCGGGCGAGGCCTTCCTGGCGCGGCGGCGGCCTGAGGGCGGTGGCGGGTCCGCGCGGCC A G STK35 Ensembl:ENSG00000125834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:2102719..2103296 26863196 MeRIP-seq:(Medium) rs762988367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659187,Human_RBP_ID_5528886,Human_RBP_ID_27820030 RMVar_hsa_circ_115283,RMVar_hsa_circ_208298 78030 RMVar_ID_78030 Human_SNP_ID_671560078 m1A Human chr20 + 2129719 2129719 2129719 AGTTTCAGTTGTGTGTAAATGAAGAAAATAGCAGAAAATGAGGACCTGCCCAAGGCGGTCAGAGA AGTTTCAGTTGTGTGTAAATGAAGAAAATAGCGGAAAATGAGGACCTGCCCAAGGCGGTCAGAGA A G STK35 Ensembl:ENSG00000125834 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2129717..2129971 26863196 MeRIP-seq:(Medium) rs1306284113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14046935 78031 RMVar_ID_78031 Human_SNP_ID_671560100 m1A Human chr20 + 2129783 2129783 2129783 AAAGGCTCTCTGAGGAGGTGGCATTGAAGCCGAGACCTGAAGGATGAGGCCTCTGCCAAGCAGAG AAAGGCTCTCTGAGGAGGTGGCATTGAAGCCGGGACCTGAAGGATGAGGCCTCTGCCAAGCAGAG A G STK35 Ensembl:ENSG00000125834 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:2129776..2129966 26863196 MeRIP-seq:(Medium) rs1018504495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14175509 78032 RMVar_ID_78032 Human_SNP_ID_671646121 m1A Human chr20 + 2467720 2467720 2467720 CGGCCGTCCTGCAGGATGCACCTCATCCTGTAATCAATATGCTGCAGCATCTTGCTGCTCTTGCC CGGCCGTCCTGCAGGATGCACCTCATCCTGTATTCAATATGCTGCAGCATCTTGCTGCTCTTGCC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:2467676..2467845 26863196 MeRIP-seq:(Medium) rs751276792 Functional Loss SNV dbSNP153 33..33 33 - - - 78033 RMVar_ID_78033 Human_SNP_ID_671646122 m1A Human chr20 + 2467724 2467724 2467724 CGTCCTGCAGGATGCACCTCATCCTGTAATCAATATGCTGCAGCATCTTGCTGCTCTTGCCCACC CGTCCTGCAGGATGCACCTCATCCTGTAATCATTATGCTGCAGCATCTTGCTGCTCTTGCCCACC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:2467487..2467854 26863196 MeRIP-seq:(Medium) rs1279957116 Functional Loss SNV dbSNP153 33..33 33 - - - 78034 RMVar_ID_78034 Human_SNP_ID_671646914 m1A Human chr20 - 2470714 2470714 2470714 GCTAGGCCTCTGAGGAGGCGAATCCGGCGGGTATCAGAGCCATCAGAACCGCCACCATGGTAAGG GCTAGGCCTCTGAGGAGGCGAATCCGGCGGGTGTCAGAGCCATCAGAACCGCCACCATGGTAAGG T C SNRPB,AL049650.2 Ensembl:ENSG00000125835,Ensembl:ENSG00000256566 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:2467626..2492733 26863410 MeRIP-seq:(Medium) rs1455457095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281244,Human_RBP_ID_560342,Human_RBP_ID_1593944,Human_RBP_ID_3644784,Human_RBP_ID_4638452,Human_RBP_ID_5118789,Human_RBP_ID_5322844,Human_RBP_ID_5471705,Human_RBP_ID_5503077,Human_RBP_ID_8853071,Human_RBP_ID_9331405,Human_RBP_ID_14052140,Human_RBP_ID_17658950,Human_RBP_ID_18193732,Human_RBP_ID_18423307,Human_RBP_ID_21895248,Human_RBP_ID_22452690,Human_RBP_ID_22816919,Human_RBP_ID_23133539,Human_RBP_ID_26488978,Human_RBP_ID_27018206,Human_RBP_ID_27294743 Human_Splice_Rec_2054895,Human_Splice_Rec_2054907,Human_Splice_Rec_2054919 78035 RMVar_ID_78035 Human_SNP_ID_671646929 m1A Human chr20 - 2470731 2470731 2470731 TCGGCTGTGGGAGAGAGGCTAGGCCTCTGAGGAGGCGAATCCGGCGGGTATCAGAGCCATCAGAA TCGGCTGTGGGAGAGAGGCTAGGCCTCTGAGGCGGCGAATCCGGCGGGTATCAGAGCCATCAGAA T G SNRPB,AL049650.2 Ensembl:ENSG00000125835,Ensembl:ENSG00000256566 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr20:2467557..2492733;chr20:2470726..2470775;chr20:2470596..2470775 26863196 MeRIP-seq:(Medium) rs755530057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63577,Human_RBP_ID_560343,Human_RBP_ID_779534,Human_RBP_ID_1593944,Human_RBP_ID_3644784,Human_RBP_ID_4638452,Human_RBP_ID_5118789,Human_RBP_ID_5322844,Human_RBP_ID_9331405,Human_RBP_ID_17658950,Human_RBP_ID_18193732,Human_RBP_ID_18423277,Human_RBP_ID_21895248,Human_RBP_ID_22452690,Human_RBP_ID_22599794,Human_RBP_ID_23133539,Human_RBP_ID_23897279,Human_RBP_ID_27018206,Human_RBP_ID_27294743 Human_Splice_Rec_2054895,Human_Splice_Rec_2054907,Human_Splice_Rec_2054919 78036 RMVar_ID_78036 Human_SNP_ID_671646932 m1A Human chr20 - 2470734 2470734 2470734 AAATCGGCTGTGGGAGAGAGGCTAGGCCTCTGAGGAGGCGAATCCGGCGGGTATCAGAGCCATCA AAATCGGCTGTGGGAGAGAGGCTAGGCCTCTGGGGAGGCGAATCCGGCGGGTATCAGAGCCATCA T C SNRPB,AL049650.2 Ensembl:ENSG00000125835,Ensembl:ENSG00000256566 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:2470595..2470800 26863196 MeRIP-seq:(Medium) rs753176593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63577,Human_RBP_ID_560343,Human_RBP_ID_779534,Human_RBP_ID_1025092,Human_RBP_ID_1593944,Human_RBP_ID_3644784,Human_RBP_ID_4638452,Human_RBP_ID_5118789,Human_RBP_ID_5322844,Human_RBP_ID_9331405,Human_RBP_ID_17658950,Human_RBP_ID_18193732,Human_RBP_ID_18423277,Human_RBP_ID_21895248,Human_RBP_ID_22452690,Human_RBP_ID_22599794,Human_RBP_ID_23133539,Human_RBP_ID_23897279,Human_RBP_ID_27018206,Human_RBP_ID_27294743 Human_Splice_Rec_2054895,Human_Splice_Rec_2054907,Human_Splice_Rec_2054919 78037 RMVar_ID_78037 Human_SNP_ID_671646940 m1A Human chr20 + 2470744 2470744 2470744 GATACCCGCCGGATTCGCCTCCTCAGAGGCCTAGCCTCTCTCCCACAGCCGATTTCCCGCCGCCG GATACCCGCCGGATTCGCCTCCTCAGAGGCCTGGCCTCTCTCCCACAGCCGATTTCCCGCCGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr20:2467501..2492733;chr20:2470614..2470800 26863196 MeRIP-seq:(Medium) rs1368881659 Functional Loss SNV dbSNP153 33..33 33 - - - 78038 RMVar_ID_78038 Human_SNP_ID_671655863 m1A Human chr20 - 2508773 2508773 2508773 GCGTAGGTTAGGACGCGGGGTAGAGTGTGGCCAATGGGGAGTGCGGGTTGGAGATATTTGGTTTT GCGTAGGTTAGGACGCGGGGTAGAGTGTGGCCGATGGGGAGTGCGGGTTGGAGATATTTGGTTTT T C ZNF343,AL049650.2 Ensembl:ENSG00000088876,Ensembl:ENSG00000256566 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:2508760..2508863;chr20:2508757..2508841 26863196 MeRIP-seq:(Medium) rs6049635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23897340 GWAS_ID_9316,GWAS_ID_9317,GWAS_ID_9318,GWAS_ID_9319,GWAS_ID_9320,GWAS_ID_9321,GWAS_ID_9322,GWAS_ID_9323 RMVar_hsa_circ_101924,RMVar_hsa_circ_208308 78039 RMVar_ID_78039 Human_SNP_ID_671691318 m1A Human chr20 + 2652661 2652661 2652661 CGCATTGCGAGCCGAACCCGGGAGCTGGCGCCATGGTGAGGAGTGGTTGCGGGGCGCGGGCGACG CGCATTGCGAGCCGAACCCGGGAGCTGGCGCCCTGGTGAGGAGTGGTTGCGGGGCGCGGGCGACG A C NOP56 Ensembl:ENSG00000101361 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:2652626..2652700 26863410 MeRIP-seq:(Medium) rs1318070711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244801,Human_RBP_ID_2679907,Human_RBP_ID_4659614,Human_RBP_ID_18422799,Human_RBP_ID_19003670 Human_Splice_Rec_2055097,Human_Splice_Rec_2055123,Human_Splice_Rec_2055135,Human_Splice_Rec_2055157,Human_Splice_Rec_2055169 78040 RMVar_ID_78040 Human_SNP_ID_671691319 m1A Human chr20 + 2652661 2652661 2652661 CGCATTGCGAGCCGAACCCGGGAGCTGGCGCCATGGTGAGGAGTGGTTGCGGGGCGCGGGCGACG CGCATTGCGAGCCGAACCCGGGAGCTGGCGCCGTGGTGAGGAGTGGTTGCGGGGCGCGGGCGACG A G NOP56 Ensembl:ENSG00000101361 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:2652626..2652700 26863410 MeRIP-seq:(Medium) rs1318070711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244801,Human_RBP_ID_2679907,Human_RBP_ID_4659614,Human_RBP_ID_18422799,Human_RBP_ID_19003670 Human_Splice_Rec_2055097,Human_Splice_Rec_2055123,Human_Splice_Rec_2055135,Human_Splice_Rec_2055157,Human_Splice_Rec_2055169 78041 RMVar_ID_78041 Human_SNP_ID_671691324 m1A Human chr20 - 2652665 2652665 2652665 GTCGCGTCGCCCGCGCCCCGCAACCACTCCTCACCATGGCGCCAGCTCCCGGGTTCGGCTCGCAA GTCGCGTCGCCCGCGCCCCGCAACCACTCCTCGCCATGGCGCCAGCTCCCGGGTTCGGCTCGCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr20:2652626..2652780;chr20:2652626..2652675 26863196 MeRIP-seq:(Medium) rs1222840555 Functional Loss SNV dbSNP153 33..33 33 - - - 78042 RMVar_ID_78042 Human_SNP_ID_671691354 m1A Human chr20 + 2652691 2652685 2652691 CCATGGTGAGGAGTGGTTGCGGGGCGCGGGCGACGCGACGGTGGGGGTTTCGGCCTGCGTTCGGG CCATGGTGAGGAGTGGTTGCGGGGCGC______CGCGACGGTGGGGGTTTCGGCCTGCGTTCGGG CGGGCGA C NOP56 Ensembl:ENSG00000101361 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:2652685..2652795 26863196 MeRIP-seq:(Medium) rs781765507 Functional Loss DEL dbSNP153 28..33 33 - - - 78043 RMVar_ID_78043 Human_SNP_ID_671691561 m1A Human chr20 + 2652852 2652841 2652853 CGCGCCCCGGCTCCCGTTCCAGGTGCTGTTGCACGTGCTGTTTGAGCACGCGGTCGGCTACGCGC CGCGCCCCGGCTCCCGTTCCAG____________GTGCTGTTTGAGCACGCGGTCGGCTACGCGC GGTGCTGTTGCAC G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1363518229 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_63516,Human_RBP_ID_4659615,Human_RBP_ID_18422801,Human_RBP_ID_18769953,Human_RBP_ID_23898214 Human_Splice_Rec_2055098,Human_Splice_Rec_2055099,Human_Splice_Rec_2055124,Human_Splice_Rec_2055125,Human_Splice_Rec_2055136,Human_Splice_Rec_2055137,Human_Splice_Rec_2055158,Human_Splice_Rec_2055159,Human_Splice_Rec_2055161,Human_Splice_Rec_2055170,Human_Splice_Rec_2055171 Human_miRNA_ID_2517747 RMVar_hsa_circ_104731,RMVar_hsa_circ_118370,RMVar_hsa_circ_208313,RMVar_hsa_circ_208314 78044 RMVar_ID_78044 Human_SNP_ID_671691600 m1A Human chr20 - 2652921 2652921 2652921 GGAGCCCACGGATCTCACCCACCTGCGGCTGCAGCAGACTGATCTCCTCCACTTCCTTCAGCGCC GGAGCCCACGGATCTCACCCACCTGCGGCTGCGGCAGACTGATCTCCTCCACTTCCTTCAGCGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:2652826..2652950 26863196 MeRIP-seq:(Medium) rs777206998 Functional Loss SNV dbSNP153 33..33 33 - - - 78045 RMVar_ID_78045 Human_SNP_ID_671691601 m1A Human chr20 - 2652921 2652921 2652921 GGAGCCCACGGATCTCACCCACCTGCGGCTGCAGCAGACTGATCTCCTCCACTTCCTTCAGCGCC GGAGCCCACGGATCTCACCCACCTGCGGCTGCCGCAGACTGATCTCCTCCACTTCCTTCAGCGCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:2652826..2652950 26863196 MeRIP-seq:(Medium) rs777206998 Functional Loss SNV dbSNP153 33..33 33 - - - 78046 RMVar_ID_78046 Human_SNP_ID_671691714 m1A Human chr20 - 2653195 2653170 2653196 GGCGCAGTCAAGCAGCGGTTCTCAGCCTTGGAAGCTCTTAAAATATGCTGATACCTGGGCCCCAC GGCGCAGTCAAGCAGCGGTTCTCAGCCTTGG__________________________GGCCCCAC CCAGGTATCAGCATATTTTAAGAGCTT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr20:2653192..2653325;chr20:2653184..2653400 26863196 MeRIP-seq:(Medium) rs1319118952 Functional Loss DEL dbSNP153 32..57 33 - - - 78047 RMVar_ID_78047 Human_SNP_ID_671691738 m1A Human chr20 + 2653243 2653243 2653243 CGCTGCTTGACTGCGCCGCAGAGGCAGGAGGGAGGGAAGGAAACCACTTAGCCTCTTTCTCCCCC CGCTGCTTGACTGCGCCGCAGAGGCAGGAGGGGGGGAAGGAAACCACTTAGCCTCTTTCTCCCCC A G NOP56 Ensembl:ENSG00000101361 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:2653239..2653350 26863410 MeRIP-seq:(Medium) rs1172586549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22671228 RMVar_hsa_circ_104731,RMVar_hsa_circ_118370,RMVar_hsa_circ_208313,RMVar_hsa_circ_208314 78048 RMVar_ID_78048 Human_SNP_ID_671692235 m1A Human chr20 + 2654503 2654503 2654503 AGAAAGTACTCTTGGGAGTTGGGGATCCCAAGATTGGTGCCGCAATACAGGAGGAGTTAGGGTAC AGAAAGTACTCTTGGGAGTTGGGGATCCCAAGGTTGGTGCCGCAATACAGGAGGAGTTAGGGTAC A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2654374..2654518 26863196 MeRIP-seq:(Medium) rs1391268440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925144,Human_RBP_ID_1594167,Human_RBP_ID_9389881,Human_RBP_ID_18769979,Human_RBP_ID_19004926,Human_RBP_ID_26342300,Human_RBP_ID_27820032 Human_Splice_Rec_2055102,Human_Splice_Rec_2055103,Human_Splice_Rec_2055130,Human_Splice_Rec_2055131,Human_Splice_Rec_2055140,Human_Splice_Rec_2055141,Human_Splice_Rec_2055164,Human_Splice_Rec_2055165,Human_Splice_Rec_2055174,Human_Splice_Rec_2055175,Human_Splice_Rec_2055182,Human_Splice_Rec_2055183,Human_Splice_Rec_2055187 RMVar_hsa_circ_86547,RMVar_hsa_circ_118370,RMVar_hsa_circ_208314,RMVar_hsa_circ_95458,RMVar_hsa_circ_12818,RMVar_hsa_circ_208315,RMVar_hsa_circ_208316,RMVar_hsa_circ_39307 78049 RMVar_ID_78049 Human_SNP_ID_671692236 m1A Human chr20 + 2654503 2654503 2654503 AGAAAGTACTCTTGGGAGTTGGGGATCCCAAGATTGGTGCCGCAATACAGGAGGAGTTAGGGTAC AGAAAGTACTCTTGGGAGTTGGGGATCCCAAGTTTGGTGCCGCAATACAGGAGGAGTTAGGGTAC A T NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2654374..2654518 26863196 MeRIP-seq:(Medium) rs1391268440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925144,Human_RBP_ID_1594167,Human_RBP_ID_9389881,Human_RBP_ID_18769979,Human_RBP_ID_19004926,Human_RBP_ID_26342300,Human_RBP_ID_27820032 Human_Splice_Rec_2055102,Human_Splice_Rec_2055103,Human_Splice_Rec_2055130,Human_Splice_Rec_2055131,Human_Splice_Rec_2055140,Human_Splice_Rec_2055141,Human_Splice_Rec_2055164,Human_Splice_Rec_2055165,Human_Splice_Rec_2055174,Human_Splice_Rec_2055175,Human_Splice_Rec_2055182,Human_Splice_Rec_2055183,Human_Splice_Rec_2055187 RMVar_hsa_circ_86547,RMVar_hsa_circ_118370,RMVar_hsa_circ_208314,RMVar_hsa_circ_95458,RMVar_hsa_circ_12818,RMVar_hsa_circ_208315,RMVar_hsa_circ_208316,RMVar_hsa_circ_39307 78050 RMVar_ID_78050 Human_SNP_ID_671692812 m1A Human chr20 + 2655964 2655964 2655964 AGGTAGGTGCACGTCTCATCGCACATGCTGGCAGCCTCACCAACCTGGCCAAGTATCCAGCATCC AGGTAGGTGCACGTCTCATCGCACATGCTGGCGGCCTCACCAACCTGGCCAAGTATCCAGCATCC A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:2655926..2656000 32194978 MeRIP-seq:(Medium) rs1428414519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62484,Human_RBP_ID_560676,Human_RBP_ID_1594195,Human_RBP_ID_9388486,Human_RBP_ID_17280814,Human_RBP_ID_17968943,Human_RBP_ID_18770003,Human_RBP_ID_19003678,Human_RBP_ID_22767145,Human_RBP_ID_23898246,Human_RBP_ID_24560743,Human_RBP_ID_26342310,Human_RBP_ID_26820621 Human_Splice_Rec_2055110,Human_Splice_Rec_2055111,Human_Splice_Rec_2055148,Human_Splice_Rec_2055149,Human_Splice_Rec_2055196,Human_Splice_Rec_2055202,Human_Splice_Rec_2055208,Human_Splice_Rec_2055209,Human_Splice_Rec_2055222,Human_Splice_Rec_2055223 Human_miRNA_ID_1396421,Human_miRNA_ID_2716496,Human_miRNA_ID_2716497,Human_miRNA_ID_3052482,Human_miRNA_ID_3052483 RMVar_hsa_circ_10048,RMVar_hsa_circ_86547,RMVar_hsa_circ_118370,RMVar_hsa_circ_208314,RMVar_hsa_circ_95458,RMVar_hsa_circ_76502,RMVar_hsa_circ_12818,RMVar_hsa_circ_208315,RMVar_hsa_circ_208316,RMVar_hsa_circ_127153,RMVar_hsa_circ_208317,RMVar_hsa_circ_208318,RMVar_hsa_circ_339987,RMVar_hsa_circ_371312,RMVar_hsa_circ_85077,RMVar_hsa_circ_208319,RMVar_hsa_circ_375403,RMVar_hsa_circ_208320,RMVar_hsa_circ_208321 78051 RMVar_ID_78051 Human_SNP_ID_671692827 m1A Human chr20 - 2656017 2656017 2656017 TGCCCTCACTGGTACCTGAACAGGGCCTTTTCAGCCCCAAGGATCTGCACTGTGGATGCTGGATA TGCCCTCACTGGTACCTGAACAGGGCCTTTTCGGCCCCAAGGATCTGCACTGTGGATGCTGGATA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2655926..2656025 32194978 MeRIP-seq:(Medium) rs938389721 Functional Loss SNV dbSNP153 33..33 33 - - - 78052 RMVar_ID_78052 Human_SNP_ID_671693196 m1A Human chr20 - 2656844 2656844 2656844 ATGACATCCAGATTCTTTCGTGGTATCTCTCCAGTCTCATAGAAGGACAGTCGCTCTTCAACTTG ATGACATCCAGATTCTTTCGTGGTATCTCTCCCGTCTCATAGAAGGACAGTCGCTCTTCAACTTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2656793..2656894 32194978 MeRIP-seq:(Medium) rs779570609 Functional Loss SNV dbSNP153 33..33 33 - - - 78053 RMVar_ID_78053 Human_SNP_ID_671693305 m1A Human chr20 + 2657112 2657112 2657112 GGCAGAGGAAGCGGCTGCTGAGATTACTAGGAAGCTGGAGAAACAGGAGAAGAAACGCTTAAAGA GGCAGAGGAAGCGGCTGCTGAGATTACTAGGACGCTGGAGAAACAGGAGAAGAAACGCTTAAAGA A C NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:2657076..2657230 26863196 MeRIP-seq:(Medium) rs1158124779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560689,Human_RBP_ID_832205,Human_RBP_ID_1594219,Human_RBP_ID_1927254,Human_RBP_ID_2679944,Human_RBP_ID_3645269,Human_RBP_ID_5597045,Human_RBP_ID_6986982,Human_RBP_ID_8260321,Human_RBP_ID_8853177,Human_RBP_ID_9388500,Human_RBP_ID_10027018,Human_RBP_ID_14056137,Human_RBP_ID_17280820,Human_RBP_ID_17510897,Human_RBP_ID_17968955,Human_RBP_ID_18321192,Human_RBP_ID_18770037,Human_RBP_ID_23000371,Human_RBP_ID_24546822,Human_RBP_ID_25628800,Human_RBP_ID_26342315,Human_RBP_ID_26493939,Human_RBP_ID_27483906,Human_RBP_ID_27819519 Human_Splice_Rec_2055116,Human_Splice_Rec_2055154,Human_Splice_Rec_2055214,Human_Splice_Rec_2055220,Human_Splice_Rec_2055228,Human_Splice_Rec_2055236,Human_Splice_Rec_2055244,Human_Splice_Rec_2055252,Human_Splice_Rec_2055256,Human_Splice_Rec_2055260 Human_miRNA_ID_1189889,Human_miRNA_ID_2569696 RMVar_hsa_circ_85077,RMVar_hsa_circ_208321,RMVar_hsa_circ_56433,RMVar_hsa_circ_105665,RMVar_hsa_circ_208324 78054 RMVar_ID_78054 Human_SNP_ID_671693316 m1A Human chr20 + 2657140 2657140 2657140 AGGAAGCTGGAGAAACAGGAGAAGAAACGCTTAAAGAAGGAAAAGAAACGGCTGGCTGCACTTGC AGGAAGCTGGAGAAACAGGAGAAGAAACGCTTGAAGAAGGAAAAGAAACGGCTGGCTGCACTTGC A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2657076..2657225 26863196 MeRIP-seq:(Medium) rs748311516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62488,Human_RBP_ID_1594219,Human_RBP_ID_1927254,Human_RBP_ID_4661767,Human_RBP_ID_5594917,Human_RBP_ID_9388500,Human_RBP_ID_14056137,Human_RBP_ID_21983976,Human_RBP_ID_22817007,Human_RBP_ID_23005538,Human_RBP_ID_24546823,Human_RBP_ID_25598965,Human_RBP_ID_26342315,Human_RBP_ID_27018500,Human_RBP_ID_27294990,Human_RBP_ID_27819519 Human_Splice_Rec_2055116,Human_Splice_Rec_2055117,Human_Splice_Rec_2055154,Human_Splice_Rec_2055155,Human_Splice_Rec_2055214,Human_Splice_Rec_2055215,Human_Splice_Rec_2055220,Human_Splice_Rec_2055228,Human_Splice_Rec_2055229,Human_Splice_Rec_2055236,Human_Splice_Rec_2055237,Human_Splice_Rec_2055244,Human_Splice_Rec_2055245,Human_Splice_Rec_2055252,Human_Splice_Rec_2055256,Human_Splice_Rec_2055260,Human_Splice_Rec_2055261,Human_Splice_Rec_2055263 RMVar_hsa_circ_85077,RMVar_hsa_circ_208321,RMVar_hsa_circ_56433,RMVar_hsa_circ_105665,RMVar_hsa_circ_208324 78055 RMVar_ID_78055 Human_SNP_ID_671693330 m1A Human chr20 - 2657160 2657160 2657160 TGTTTTCTGAAGACGCGAGGGCAAGTGCAGCCAGCCGTTTCTTTTCCTTCTTTAAGCGTTTCTTC TGTTTTCTGAAGACGCGAGGGCAAGTGCAGCCGGCCGTTTCTTTTCCTTCTTTAAGCGTTTCTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:2657056..2657236 26863196 MeRIP-seq:(Medium) rs776964549 Functional Loss SNV dbSNP153 33..33 33 - - - 78056 RMVar_ID_78056 Human_SNP_ID_671693620 m1A Human chr20 - 2657896 2657896 2657896 CTAAAGGGAAGGACAGGGGAACAGGCTGTGAGAACAGTGCTCATTACATCTTCAGCAATTAAGTA CTAAAGGGAAGGACAGGGGAACAGGCTGTGAGCACAGTGCTCATTACATCTTCAGCAATTAAGTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:2657881..2658025 26863196 MeRIP-seq:(Medium) rs1479948927 Functional Loss SNV dbSNP153 33..33 33 - - - 78057 RMVar_ID_78057 Human_SNP_ID_671693898 m1A Human chr20 - 2658517 2658517 2658517 ATGGATGATGATGATTCTCCCCCACAGGTTCGAACCTCTGACATGGGTGGCTATGCTACTTGCCA ATGGATGATGATGATTCTCCCCCACAGGTTCGGACCTCTGACATGGGTGGCTATGCTACTTGCCA T C IDH3B Ensembl:ENSG00000101365 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs563728009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560708,Human_RBP_ID_1594252,Human_RBP_ID_5148014,Human_RBP_ID_5323141,Human_RBP_ID_5382833,Human_RBP_ID_8529830,Human_RBP_ID_18167619,Human_RBP_ID_19105847,Human_RBP_ID_23212228 Human_Splice_Rec_2055274,Human_Splice_Rec_2055282,Human_Splice_Rec_2055368 RMVar_hsa_circ_88903,RMVar_hsa_circ_93887,RMVar_hsa_circ_105929,RMVar_hsa_circ_124535,RMVar_hsa_circ_114567,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_89412,RMVar_hsa_circ_208326,RMVar_hsa_circ_208330,RMVar_hsa_circ_208332,RMVar_hsa_circ_208334,RMVar_hsa_circ_83240,RMVar_hsa_circ_208333,RMVar_hsa_circ_208331,RMVar_hsa_circ_208328,RMVar_hsa_circ_208329,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325 78058 RMVar_ID_78058 Human_SNP_ID_671693939 m1A Human chr20 - 2658574 2658574 2658574 CTTAGGGGACAGACTGTTGGGTGGTGATGGGGATTGTTAGGATGGAGCCCAGGCCACATGGATGA CTTAGGGGACAGACTGTTGGGTGGTGATGGGGGTTGTTAGGATGGAGCCCAGGCCACATGGATGA T C IDH3B Ensembl:ENSG00000101365 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:2658526..2658725 32194978 MeRIP-seq:(Medium) rs367573436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9736,Human_RBP_ID_832089,Human_RBP_ID_1927278,Human_RBP_ID_3645281,Human_RBP_ID_5147839,Human_RBP_ID_5323141,Human_RBP_ID_5382519,Human_RBP_ID_6987007,Human_RBP_ID_9353992,Human_RBP_ID_17968968,Human_RBP_ID_18167619,Human_RBP_ID_19105848,Human_RBP_ID_22670652,Human_RBP_ID_23212228,Human_RBP_ID_23898284 RMVar_hsa_circ_88903,RMVar_hsa_circ_93887,RMVar_hsa_circ_105929,RMVar_hsa_circ_124535,RMVar_hsa_circ_114567,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_89412,RMVar_hsa_circ_208326,RMVar_hsa_circ_208330,RMVar_hsa_circ_208332,RMVar_hsa_circ_208334,RMVar_hsa_circ_83240,RMVar_hsa_circ_208333,RMVar_hsa_circ_208331,RMVar_hsa_circ_208328,RMVar_hsa_circ_208329,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325 78059 RMVar_ID_78059 Human_SNP_ID_671694336 m1A Human chr20 - 2659577 2659577 2659577 GTTTCTTCCTGTCCATATCCACAGTCTTGAGTATCACTCCAGCATGATCGCAGATGCGGTGAAGA GTTTCTTCCTGTCCATATCCACAGTCTTGAGTGTCACTCCAGCATGATCGCAGATGCGGTGAAGA T C IDH3B Ensembl:ENSG00000101365 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2659526..2659600 32194978 MeRIP-seq:(Medium) rs1568547187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1927280,Human_RBP_ID_3960021,Human_RBP_ID_5382835,Human_RBP_ID_19003682 Human_Splice_Rec_2055270,Human_Splice_Rec_2055271,Human_Splice_Rec_2055278,Human_Splice_Rec_2055279,Human_Splice_Rec_2055300,Human_Splice_Rec_2055301,Human_Splice_Rec_2055322,Human_Splice_Rec_2055323,Human_Splice_Rec_2055344,Human_Splice_Rec_2055345,Human_Splice_Rec_2055366,Human_Splice_Rec_2055367,Human_Splice_Rec_2055374,Human_Splice_Rec_2055375,Human_Splice_Rec_2055396,Human_Splice_Rec_2055397,Human_Splice_Rec_2055400 RMVar_hsa_circ_88903,RMVar_hsa_circ_93887,RMVar_hsa_circ_105929,RMVar_hsa_circ_124535,RMVar_hsa_circ_114567,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_208326,RMVar_hsa_circ_208330,RMVar_hsa_circ_208332,RMVar_hsa_circ_83240,RMVar_hsa_circ_208333,RMVar_hsa_circ_208331,RMVar_hsa_circ_208328,RMVar_hsa_circ_208329,RMVar_hsa_circ_208327,RMVar_hsa_circ_21850,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_63077,RMVar_hsa_circ_208335 78060 RMVar_ID_78060 Human_SNP_ID_671694834 m1A Human chr20 + 2660959 2660959 2660959 GAGGCTAGCTCCCCCTTATACTCCATCGGGGTATGAATCTTTCCTGTGAAAACAAAGTGGGAAAA GAGGCTAGCTCCCCCTTATACTCCATCGGGGTGTGAATCTTTCCTGTGAAAACAAAGTGGGAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2660901..2660975 32194978 MeRIP-seq:(Medium) rs150756817 Functional Loss SNV dbSNP153 33..33 33 - - - 78061 RMVar_ID_78061 Human_SNP_ID_671695536 m1A Human chr20 - 2663538 2663538 2663538 GAAGGCTGCCGCTGTCCCAGTGGAGTTCCAGGAGCACCACCTGAGTGAGGTGCAGAATATGGCAT GAAGGCTGCCGCTGTCCCAGTGGAGTTCCAGGGGCACCACCTGAGTGAGGTGCAGAATATGGCAT T C IDH3B Ensembl:ENSG00000101365 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:2663451..2663575 32194978 MeRIP-seq:(Medium) rs1013250648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560721,Human_RBP_ID_925161,Human_RBP_ID_9388525,Human_RBP_ID_19003688,Human_RBP_ID_22452858,Human_RBP_ID_23005075 Human_Splice_Rec_2055288,Human_Splice_Rec_2055289,Human_Splice_Rec_2055308,Human_Splice_Rec_2055309,Human_Splice_Rec_2055330,Human_Splice_Rec_2055331,Human_Splice_Rec_2055352,Human_Splice_Rec_2055353,Human_Splice_Rec_2055382,Human_Splice_Rec_2055383,Human_Splice_Rec_2055408,Human_Splice_Rec_2055409,Human_Splice_Rec_2055418,Human_Splice_Rec_2055419 Human_miRNA_ID_2771384 RMVar_hsa_circ_88903,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_208326,RMVar_hsa_circ_208328,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_208335,RMVar_hsa_circ_96097,RMVar_hsa_circ_208340 78062 RMVar_ID_78062 Human_SNP_ID_671695623 m1A Human chr20 - 2663751 2663751 2663751 CTTCTCCCCTCTTCCCCCAATTGAGGCCGAGGACGTGAGGGTGGAGGGCTCCTTTCCCGTGACCA CTTCTCCCCTCTTCCCCCAATTGAGGCCGAGGCCGTGAGGGTGGAGGGCTCCTTTCCCGTGACCA T G IDH3B Ensembl:ENSG00000101365 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2663701..2663775 26863196 MeRIP-seq:(Medium) rs769053652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8942862,Human_RBP_ID_19003690 Human_Splice_Rec_2055286,Human_Splice_Rec_2055287,Human_Splice_Rec_2055306,Human_Splice_Rec_2055307,Human_Splice_Rec_2055328,Human_Splice_Rec_2055329,Human_Splice_Rec_2055350,Human_Splice_Rec_2055351,Human_Splice_Rec_2055380,Human_Splice_Rec_2055381,Human_Splice_Rec_2055406,Human_Splice_Rec_2055407,Human_Splice_Rec_2055416,Human_Splice_Rec_2055417 RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_208326,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_208335,RMVar_hsa_circ_96097,RMVar_hsa_circ_208340 78063 RMVar_ID_78063 Human_SNP_ID_671695746 m1A Human chr20 + 2664001 2664001 2664001 CTCTCCATGCCCCAGGGTTCCCGGCGGAGACCAGCGCCTGCAACAGGGACACACAAGCCTGTAAG CTCTCCATGCCCCAGGGTTCCCGGCGGAGACCGGCGCCTGCAACAGGGACACACAAGCCTGTAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:2663926..2664025 26863196 MeRIP-seq:(Medium) rs149148826 Functional Loss SNV dbSNP153 33..33 33 - - - 78064 RMVar_ID_78064 Human_SNP_ID_671695750 m1A Human chr20 - 2664007 2664007 2664007 GCTGACCTTACAGGCTTGTGTGTCCCTGTTGCAGGCGCTGGTCTCCGCCGGGAACCCTGGGGCAT GCTGACCTTACAGGCTTGTGTGTCCCTGTTGCCGGCGCTGGTCTCCGCCGGGAACCCTGGGGCAT T G IDH3B Ensembl:ENSG00000101365 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:2663901..2664025 26863196 MeRIP-seq:(Medium) rs1568552186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660079,Human_RBP_ID_5384430,Human_RBP_ID_22670656 Human_Splice_Rec_2055285,Human_Splice_Rec_2055305,Human_Splice_Rec_2055327,Human_Splice_Rec_2055349,Human_Splice_Rec_2055379,Human_Splice_Rec_2055405,Human_Splice_Rec_2055415 RMVar_hsa_circ_92565,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_208336 78065 RMVar_ID_78065 Human_SNP_ID_671719111 m1A Human chr20 - 2755627 2755627 2755627 AGGCAGCCGCCAGCGGGGGGCTAGAGGGCATGACTCCGGGGCGGGGCGGGGAGGGGCAGGCGCAG AGGCAGCCGCCAGCGGGGGGCTAGAGGGCATGCCTCCGGGGCGGGGCGGGGAGGGGCAGGCGCAG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:2755623..2755766 26863196 MeRIP-seq:(Medium) rs1384068690 Functional Loss SNV dbSNP153 33..33 33 - - - 78066 RMVar_ID_78066 Human_SNP_ID_671740982 m1A Human chr20 - 2836220 2836220 2836220 CCAGACTTCGGGGAGCACCTGGCCTTGCTCCCACCCCCACCTTCTTCTTTGCCTCCTCCCATGCC CCAGACTTCGGGGAGCACCTGGCCTTGCTCCCCCCCCCACCTTCTTCTTTGCCTCCTCCCATGCC T G PCED1A Ensembl:ENSG00000132635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:2836169..2836252 26863196 MeRIP-seq:(Medium) rs1475338218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18950179 Human_Splice_Rec_2055602,Human_Splice_Rec_2055614 RMVar_hsa_circ_123458,RMVar_hsa_circ_208347 78067 RMVar_ID_78067 Human_SNP_ID_671740987 m1A Human chr20 + 2836233 2836233 2836233 GCAAAGAAGAAGGTGGGGGTGGGAGCAAGGCCAGGTGCTCCCCGAAGTCTGGGGTCTGCCTATGG GCAAAGAAGAAGGTGGGGGTGGGAGCAAGGCCGGGTGCTCCCCGAAGTCTGGGGTCTGCCTATGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:2836052..2836260 26863196 MeRIP-seq:(Medium) rs1425795656 Functional Loss SNV dbSNP153 33..33 33 - - - 78068 RMVar_ID_78068 Human_SNP_ID_671741386 m1A Human chr20 - 2837884 2837884 2837884 CATGGGTGTGAGGAGTGGAAAGACAGGGAGGAAGGGCCATCCAGGCAGTGTGGCAGAAGCAAAGA CATGGGTGTGAGGAGTGGAAAGACAGGGAGGAGGGGCCATCCAGGCAGTGTGGCAGAAGCAAAGA T C PCED1A Ensembl:ENSG00000132635 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2837849..2837956 26863196 MeRIP-seq:(Medium) rs976653243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5200951,Human_RBP_ID_5472164,Human_RBP_ID_6987160,Human_RBP_ID_22722442,Human_RBP_ID_23898370 RMVar_hsa_circ_123458,RMVar_hsa_circ_208347 78069 RMVar_ID_78069 Human_SNP_ID_671751831 m1A Human chr20 + 2873648 2873648 2873648 GGCGAGGCCGCCGCCGCCGCCGCGGGGCTCGGAGCCGCGGGCCGGGCGGCGGCCCTGAGGGCTAG GGCGAGGCCGCCGCCGCCGCCGCGGGGCTCGGGGCCGCGGGCCGGGCGGCGGCCCTGAGGGCTAG A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:2873551..2873775 26863410 MeRIP-seq:(Medium) rs894158016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659191 RMVar_hsa_circ_125467,RMVar_hsa_circ_208366 78070 RMVar_ID_78070 Human_SNP_ID_671772949 m1A Human chr20 + 2958257 2958257 2958257 TAGAAAGTGTGGTTGGAGAGTGGGAAGGCAAGATTTATTCAGTATGGGGGCTTTTCTGGGTGATG TAGAAAGTGTGGTTGGAGAGTGGGAAGGCAAGTTTTATTCAGTATGGGGGCTTTTCTGGGTGATG A T PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:2958250..2958386 26863196 MeRIP-seq:(Medium) rs1164537361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72082,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_340487,RMVar_hsa_circ_208367,RMVar_hsa_circ_331833,RMVar_hsa_circ_280049,RMVar_hsa_circ_14343,RMVar_hsa_circ_208372,RMVar_hsa_circ_65322,RMVar_hsa_circ_325596,RMVar_hsa_circ_208371,RMVar_hsa_circ_332747,RMVar_hsa_circ_277239,RMVar_hsa_circ_208373,RMVar_hsa_circ_361705 78071 RMVar_ID_78071 Human_SNP_ID_671779953 m1A Human chr20 - 2988101 2988101 2988101 TTCCCCATGACATTAAGGAATGCCTTACCCACATCCTCAGTGCGGCCGTTGGATAAGCGGAAAGA TTCCCCATGACATTAAGGAATGCCTTACCCACGTCCTCAGTGCGGCCGTTGGATAAGCGGAAAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2988051..2988125 32194978 MeRIP-seq:(Medium) rs1330796523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208385 78072 RMVar_ID_78072 Human_SNP_ID_671789115 m1A Human chr20 + 3024551 3024551 3024551 TGGAGATACAGAACTGGAAGTGACCTCTCTAGAAACCCACCTGCAGAAAATTTACAACAAAATCC TGGAGATACAGAACTGGAAGTGACCTCTCTAGGAACCCACCTGCAGAAAATTTACAACAAAATCC A G PTPRA Ensembl:ENSG00000132670 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:3024501..3024575 32194978 MeRIP-seq:(Medium) rs1243121439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1927386 Human_Splice_Rec_2055828,Human_Splice_Rec_2055829,Human_Splice_Rec_2055884,Human_Splice_Rec_2055885,Human_Splice_Rec_2055930,Human_Splice_Rec_2055931,Human_Splice_Rec_2055994,Human_Splice_Rec_2055995,Human_Splice_Rec_2056038,Human_Splice_Rec_2056039 Human_miRNA_ID_2798060,Human_miRNA_ID_2799024,Human_miRNA_ID_2800407,Human_miRNA_ID_2807720,Human_miRNA_ID_2810864,Human_miRNA_ID_2814006,Human_miRNA_ID_2833598,Human_miRNA_ID_2853119,Human_miRNA_ID_2854181,Human_miRNA_ID_2861265 RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_66766,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_43987,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_208389 78073 RMVar_ID_78073 Human_SNP_ID_671795040 m1A Human chr20 + 3046160 3046151 3046161 GGTGCTGCCAGCGCGCGGCCGCAAGACCCGCCACGACCCGCTGGCCAAATCCAAGATCGAGCGAG GGTGCTGCCAGCGCGCGGCCGCAA__________GACCCGCTGGCCAAATCCAAGATCGAGCGAG AGACCCGCCAC A MRPS26 Ensembl:ENSG00000125901 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:3046051..3046200 26863410 MeRIP-seq:(Medium) rs745906991 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_244433,Human_RBP_ID_4640028 RMVar_hsa_circ_78926,RMVar_hsa_circ_208391 78074 RMVar_ID_78074 Human_SNP_ID_671795043 m1A Human chr20 + 3046153 3046153 3046153 CCCCTCTGGTGCTGCCAGCGCGCGGCCGCAAGACCCGCCACGACCCGCTGGCCAAATCCAAGATC CCCCTCTGGTGCTGCCAGCGCGCGGCCGCAAGCCCCGCCACGACCCGCTGGCCAAATCCAAGATC A C MRPS26 Ensembl:ENSG00000125901 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:3046051..3046225 26863410 MeRIP-seq:(Medium) rs1004502117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244433,Human_RBP_ID_4640027 Human_miRNA_ID_2158155,Human_miRNA_ID_2611825 RMVar_hsa_circ_78926,RMVar_hsa_circ_208391 78075 RMVar_ID_78075 Human_SNP_ID_671795044 m1A Human chr20 + 3046153 3046153 3046153 CCCCTCTGGTGCTGCCAGCGCGCGGCCGCAAGACCCGCCACGACCCGCTGGCCAAATCCAAGATC CCCCTCTGGTGCTGCCAGCGCGCGGCCGCAAGGCCCGCCACGACCCGCTGGCCAAATCCAAGATC A G MRPS26 Ensembl:ENSG00000125901 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:3046051..3046225 26863410 MeRIP-seq:(Medium) rs1004502117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244433,Human_RBP_ID_4640027 Human_miRNA_ID_2158155,Human_miRNA_ID_2611825 RMVar_hsa_circ_78926,RMVar_hsa_circ_208391 78076 RMVar_ID_78076 Human_SNP_ID_671795050 m1A Human chr20 + 3046160 3046160 3046160 GGTGCTGCCAGCGCGCGGCCGCAAGACCCGCCACGACCCGCTGGCCAAATCCAAGATCGAGCGAG GGTGCTGCCAGCGCGCGGCCGCAAGACCCGCCGCGACCCGCTGGCCAAATCCAAGATCGAGCGAG A G MRPS26 Ensembl:ENSG00000125901 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:3046051..3046200 26863410 MeRIP-seq:(Medium) rs771761734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244433,Human_RBP_ID_4640028 RMVar_hsa_circ_78926,RMVar_hsa_circ_208391 78077 RMVar_ID_78077 Human_SNP_ID_671795057 m1A Human chr20 - 3046169 3046169 3046169 GCATGTTCACTCGCTCGATCTTGGATTTGGCCAGCGGGTCGTGGCGGGTCTTGCGGCCGCGCGCT GCATGTTCACTCGCTCGATCTTGGATTTGGCCGGCGGGTCGTGGCGGGTCTTGCGGCCGCGCGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:3046051..3046342 26863196 MeRIP-seq:(Medium) rs766218017 Functional Loss SNV dbSNP153 33..33 33 - - - 78078 RMVar_ID_78078 Human_SNP_ID_671795290 m1A Human chr20 + 3046604 3046604 3046604 AAGCCCGGGCCCCGCTCAGCCTCGGCCCTTTGACCCTCACAGGATAGCGAGGCTGCGGCAGGAGG AAGCCCGGGCCCCGCTCAGCCTCGGCCCTTTGCCCCTCACAGGATAGCGAGGCTGCGGCAGGAGG A C MRPS26 Ensembl:ENSG00000125901 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3046601..3046650 26863196 MeRIP-seq:(Medium) rs1193760877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923831,Human_RBP_ID_5200153,Human_RBP_ID_5382524,Human_RBP_ID_19109745,Human_RBP_ID_22549667 RMVar_hsa_circ_89020,RMVar_hsa_circ_78926,RMVar_hsa_circ_208391,RMVar_hsa_circ_208392 78079 RMVar_ID_78079 Human_SNP_ID_671795291 m1A Human chr20 + 3046604 3046604 3046604 AAGCCCGGGCCCCGCTCAGCCTCGGCCCTTTGACCCTCACAGGATAGCGAGGCTGCGGCAGGAGG AAGCCCGGGCCCCGCTCAGCCTCGGCCCTTTGGCCCTCACAGGATAGCGAGGCTGCGGCAGGAGG A G MRPS26 Ensembl:ENSG00000125901 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3046601..3046650 26863196 MeRIP-seq:(Medium) rs1193760877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923831,Human_RBP_ID_5200153,Human_RBP_ID_5382524,Human_RBP_ID_19109745,Human_RBP_ID_22549667 RMVar_hsa_circ_89020,RMVar_hsa_circ_78926,RMVar_hsa_circ_208391,RMVar_hsa_circ_208392 78080 RMVar_ID_78080 Human_SNP_ID_671795343 m1A Human chr20 + 3046686 3046686 3046686 CGGCAGGCGTTGGAGCAGGCCCGCAAGGCCGAAGAGGTGCAGGCCTGGGCGCAGCGCAAGGAGCG CGGCAGGCGTTGGAGCAGGCCCGCAAGGCCGAGGAGGTGCAGGCCTGGGCGCAGCGCAAGGAGCG A G MRPS26 Ensembl:ENSG00000125901 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3046026..3048137 26863196 MeRIP-seq:(Medium) rs780197156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9331757,Human_RBP_ID_9353993,Human_RBP_ID_9388542,Human_RBP_ID_19003713,Human_RBP_ID_19105876 Human_Splice_Rec_2056076,Human_Splice_Rec_2056077 RMVar_hsa_circ_89020,RMVar_hsa_circ_78926,RMVar_hsa_circ_208391,RMVar_hsa_circ_208392 78081 RMVar_ID_78081 Human_SNP_ID_671813443 m1A Human chr20 - 3111535 3111535 3111535 TGGACTCTAAAAGTTGAGACTGGTGTGAAGAGAGGTGAGGAGGCTGGGTGGGCCGTGCAGGGAGT TGGACTCTAAAAGTTGAGACTGGTGTGAAGAGGGGTGAGGAGGCTGGGTGGGCCGTGCAGGGAGT T C UBOX5 Ensembl:ENSG00000185019 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3111496..3111625 26863196 MeRIP-seq:(Medium) rs1460786125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75957,RMVar_hsa_circ_208394 78082 RMVar_ID_78082 Human_SNP_ID_671814680 m1A Human chr20 + 3116209 3116209 3116209 TCCACCCTTCTGGGGACCCCACCACCCCCCAGAGGGGTTCATCTGCATTTTCTAGGTGTTCATGT TCCACCCTTCTGGGGACCCCACCACCCCCCAGGGGGGTTCATCTGCATTTTCTAGGTGTTCATGT A G UBOX5-AS1 Ensembl:ENSG00000235958 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3116161..3116254 26863196 MeRIP-seq:(Medium) rs145493833 Functional Loss SNV dbSNP153 33..33 33 - - - 78083 RMVar_ID_78083 Human_SNP_ID_671826442 m1A Human chr20 + 3159825 3159825 3159825 ACACCAAACCGGGGACGCCGCGGGCGGCGGCGACACAGATACTGGCTCCTCCGGCGACTCCGAGC ACACCAAACCGGGGACGCCGCGGGCGGCGGCGTCACAGATACTGGCTCCTCCGGCGACTCCGAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3159759..3159830 26863196 MeRIP-seq:(Medium) rs1420329979 Functional Loss SNV dbSNP153 33..33 33 - - - 78084 RMVar_ID_78084 Human_SNP_ID_671826445 m1A Human chr20 + 3159833 3159833 3159833 CCGGGGACGCCGCGGGCGGCGGCGACACAGATACTGGCTCCTCCGGCGACTCCGAGCCTCACAGC CCGGGGACGCCGCGGGCGGCGGCGACACAGATGCTGGCTCCTCCGGCGACTCCGAGCCTCACAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:3159764..3159853 26863196 MeRIP-seq:(Medium) rs965773296 Functional Loss SNV dbSNP153 33..33 33 - - - 78085 RMVar_ID_78085 Human_SNP_ID_671827673 m1A Human chr20 - 3164651 3164648 3164651 TCGCCGAGGAGCGCCGCGTGTGGCTGGAGGAGAAGGAGAAGGTGATCGAGTACCAGAAGCAGCTG TCGCCGAGGAGCGCCGCGTGTGGCTGGAGGAG___GAGAAGGTGATCGAGTACCAGAAGCAGCTG CCTT C LZTS3 Ensembl:ENSG00000088899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3164509..3164864 26863196 MeRIP-seq:(Medium) rs1261295257 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_21983442 78086 RMVar_ID_78086 Human_SNP_ID_671827716 m1A Human chr20 - 3164749 3164738 3164750 CGGGGAGAGCGGGACGCGGGCCCTGCGGCGGGAGGTGGGGCGGCTGCAGGCCGAGCTGGCGGCTG CGGGGAGAGCGGGACGCGGGCCCTGCGGCGG____________CTGCAGGCCGAGCTGGCGGCTG GCCGCCCCACCTC G LZTS3 Ensembl:ENSG00000088899 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:3164551..3164798 26863196 MeRIP-seq:(Medium) rs1258072370 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_244714,Human_RBP_ID_561690,Human_RBP_ID_831388,Human_RBP_ID_5528891,Human_RBP_ID_9353994,Human_RBP_ID_21982742,Human_RBP_ID_22722841 78087 RMVar_ID_78087 Human_SNP_ID_671827722 m1A Human chr20 - 3164749 3164749 3164749 CGGGGAGAGCGGGACGCGGGCCCTGCGGCGGGAGGTGGGGCGGCTGCAGGCCGAGCTGGCGGCTG CGGGGAGAGCGGGACGCGGGCCCTGCGGCGGGGGGTGGGGCGGCTGCAGGCCGAGCTGGCGGCTG T C LZTS3 Ensembl:ENSG00000088899 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:3164551..3164798 26863196 MeRIP-seq:(Medium) rs914301822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244714,Human_RBP_ID_561690,Human_RBP_ID_831388,Human_RBP_ID_5528891,Human_RBP_ID_9353994,Human_RBP_ID_21982742,Human_RBP_ID_22722841 78088 RMVar_ID_78088 Human_SNP_ID_671828141 m1A Human chr20 - 3165738 3165738 3165738 CCAGGTACTGGAGGAGCGGCAGAAGGCGTGGGAGCGGGAGCTGGCCGAGCTGCGGCAGGGCTGCA CCAGGTACTGGAGGAGCGGCAGAAGGCGTGGGGGCGGGAGCTGGCCGAGCTGCGGCAGGGCTGCA T C LZTS3 Ensembl:ENSG00000088899 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3165063..3165848 26863196 MeRIP-seq:(Medium) rs779257379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831326,Human_RBP_ID_4641700,Human_RBP_ID_5528893,Human_RBP_ID_9389942,Human_RBP_ID_19004998,Human_RBP_ID_23004927 78089 RMVar_ID_78089 Human_SNP_ID_671830446 m1A Human chr20 - 3173547 3173547 3173547 AGGAGGGGCGCGGAGCGGAGCCGGGCCCGCGCAGCGCGCCCCGCCGGGCGTGCTTCGGGCTGCGC AGGAGGGGCGCGGAGCGGAGCCGGGCCCGCGCGGCGCGCCCCGCCGGGCGTGCTTCGGGCTGCGC T C LZTS3 Ensembl:ENSG00000088899 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3173409..3173571 26863196 MeRIP-seq:(Medium) rs1027521972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3655587,Human_RBP_ID_4659198 Human_Splice_Rec_2056129,Human_Splice_Rec_2056139,Human_Splice_Rec_2056149 78090 RMVar_ID_78090 Human_SNP_ID_671834735 m1A Human chr20 - 3190810 3190810 3190810 CCACAACCTGCATGTCCCCACAGGTGTGATTGACGACCGGGGCAAGTTCATCTACATAACCCCAG CCACAACCTGCATGTCCCCACAGGTGTGATTGGCGACCGGGGCAAGTTCATCTACATAACCCCAG T C DDRGK1 Ensembl:ENSG00000198171 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:3190655..3190860;chr20:3190692..3190864 26863196 MeRIP-seq:(Medium) rs1277162266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1595019,Human_RBP_ID_18770809,Human_RBP_ID_22453669,Human_RBP_ID_23900073,Human_RBP_ID_27295699 Human_Splice_Rec_2056158,Human_Splice_Rec_2056172,Human_Splice_Rec_2056178 78091 RMVar_ID_78091 Human_SNP_ID_671835047 m1A Human chr20 - 3191814 3191814 3191814 TTTCTTTTCCTCCTTCTTTTTGTAGCAGTCCAAGGTTGTGCTCTTGGAAGACCTGGCTTCCCAGG TTTCTTTTCCTCCTTCTTTTTGTAGCAGTCCAGGGTTGTGCTCTTGGAAGACCTGGCTTCCCAGG T C DDRGK1 Ensembl:ENSG00000198171 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:3191751..3191825 26863196 MeRIP-seq:(Medium) rs968162741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923839,Human_RBP_ID_1595029,Human_RBP_ID_1927959,Human_RBP_ID_3960032,Human_RBP_ID_5382841,Human_RBP_ID_8260344,Human_RBP_ID_9389946,Human_RBP_ID_14069009,Human_RBP_ID_24560701,Human_RBP_ID_25626728,Human_RBP_ID_27295700,Human_RBP_ID_27819538 Human_Splice_Rec_2056168,Human_Splice_Rec_2056169,Human_Splice_Rec_2056176,Human_Splice_Rec_2056177,Human_Splice_Rec_2056188 RMVar_hsa_circ_303108,RMVar_hsa_circ_364112 78092 RMVar_ID_78092 Human_SNP_ID_671839124 m1A Human chr20 - 3204642 3204642 3204642 TCCCGGCCTCAGGGTGGACGCAGTGGTTCTGCACTGAGGCCCTCGTCATGGTGGCGCCTGTGTGG TCCCGGCCTCAGGGTGGACGCAGTGGTTCTGCGCTGAGGCCCTCGTCATGGTGGCGCCTGTGTGG T C DDRGK1 Ensembl:ENSG00000198171 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:3204525..3204652 26863196 MeRIP-seq:(Medium) rs1329465662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1595039,Human_RBP_ID_4641847,Human_RBP_ID_5503189,Human_RBP_ID_8853747 78093 RMVar_ID_78093 Human_SNP_ID_671840487 m1A Human chr20 + 3209552 3209552 3209552 TCGGTGGCTCAGCTGGGTAACCGGGGATCACCATGGCGGCCTCATTGGTGGGGAAGAAGATCGTG TCGGTGGCTCAGCTGGGTAACCGGGGATCACCGTGGCGGCCTCATTGGTGGGGAAGAAGATCGTG A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3209501..3209891 26863196 MeRIP-seq:(Medium) rs776199615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4641860,Human_RBP_ID_9331412,Human_RBP_ID_18422804,Human_RBP_ID_22080491,Human_RBP_ID_23900131 Human_Splice_Rec_2056223,Human_Splice_Rec_2056237,Human_Splice_Rec_2056245,Human_Splice_Rec_2056259,Human_Splice_Rec_2056271 RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 78094 RMVar_ID_78094 Human_SNP_ID_671840494 m1A Human chr20 - 3209564 3209564 3209564 CCCCGTTACAAACACGATCTTCTTCCCCACCAATGAGGCCGCCATGGTGATCCCCGGTTACCCAG CCCCGTTACAAACACGATCTTCTTCCCCACCAGTGAGGCCGCCATGGTGATCCCCGGTTACCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:3209476..3213189 26863196 MeRIP-seq:(Medium) rs762598981 Functional Loss SNV dbSNP153 33..33 33 - - - 78095 RMVar_ID_78095 Human_SNP_ID_671841378 m1A Human chr20 - 3212928 3212928 3212928 CAGGTCTCTGCTTGTGCTAAGCCCCCATCCAGAACACACTCTTCTCTTCTCAATGCTCCCAGAAA CAGGTCTCTGCTTGTGCTAAGCCCCCATCCAGGACACACTCTTCTCTTCTCAATGCTCCCAGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3212924..3213073 26863196 MeRIP-seq:(Medium) rs527750672 Functional Loss SNV dbSNP153 33..33 33 - - - 78096 RMVar_ID_78096 Human_SNP_ID_671843053 m1A Human chr20 + 3218592 3218592 3218592 TGCGCTCTGCACGTTTGCACTCAGCACCGGGGACCCAAGCCAGCCCGTGCGCCTGTTCAGGGGCC TGCGCTCTGCACGTTTGCACTCAGCACCGGGGTCCCAAGCCAGCCCGTGCGCCTGTTCAGGGGCC A T ITPA Ensembl:ENSG00000125877 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3218528..3218677 32194978 MeRIP-seq:(Medium) rs1276150567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9389953,Human_RBP_ID_14071139,Human_RBP_ID_18770885,Human_RBP_ID_23900237,Human_RBP_ID_27484576 Human_Splice_Rec_2056196,Human_Splice_Rec_2056197,Human_Splice_Rec_2056210,Human_Splice_Rec_2056218,Human_Splice_Rec_2056219,Human_Splice_Rec_2056232,Human_Splice_Rec_2056233,Human_Splice_Rec_2056244,Human_Splice_Rec_2056254,Human_Splice_Rec_2056255,Human_Splice_Rec_2056266,Human_Splice_Rec_2056267,Human_Splice_Rec_2056276,Human_Splice_Rec_2056277,Human_Splice_Rec_2056282,Human_Splice_Rec_2056283 RMVar_hsa_circ_76640,RMVar_hsa_circ_208399,RMVar_hsa_circ_106937,RMVar_hsa_circ_78223,RMVar_hsa_circ_348105,RMVar_hsa_circ_208400,RMVar_hsa_circ_208401,RMVar_hsa_circ_95783,RMVar_hsa_circ_22999,RMVar_hsa_circ_95926,RMVar_hsa_circ_208403,RMVar_hsa_circ_292837,RMVar_hsa_circ_87549,RMVar_hsa_circ_208405,RMVar_hsa_circ_208406,RMVar_hsa_circ_208404 78097 RMVar_ID_78097 Human_SNP_ID_671863517 m1A Human chr20 - 3291811 3291811 3291811 GGGGTACGGTGTAGAGGCCCTGGTCAGAGGGAACAAGAGACAGCTTCTGGGTCCTACAAAAGAAG GGGGTACGGTGTAGAGGCCCTGGTCAGAGGGAGCAAGAGACAGCTTCTGGGTCCTACAAAAGAAG T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3291804..3291919 26863196 MeRIP-seq:(Medium) rs375877433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10209,RMVar_hsa_circ_98391,RMVar_hsa_circ_208414,RMVar_hsa_circ_336893,RMVar_hsa_circ_8916,RMVar_hsa_circ_362993,RMVar_hsa_circ_38395,RMVar_hsa_circ_208416,RMVar_hsa_circ_208417,RMVar_hsa_circ_280352,RMVar_hsa_circ_286653,RMVar_hsa_circ_208424,RMVar_hsa_circ_312616,RMVar_hsa_circ_50634,RMVar_hsa_circ_12905,RMVar_hsa_circ_20089,RMVar_hsa_circ_338159,RMVar_hsa_circ_347147,RMVar_hsa_circ_16214,RMVar_hsa_circ_284069,RMVar_hsa_circ_208425,RMVar_hsa_circ_12726 78098 RMVar_ID_78098 Human_SNP_ID_671893027 m1A Human chr20 - 3407604 3407604 3407604 GCTAGCGTGGAGCCGCCCTGCGGGCAACTGAGACCCTCGCAGCTGCACCGTCCTCCTCCGCCGCC GCTAGCGTGGAGCCGCCCTGCGGGCAACTGAGGCCCTCGCAGCTGCACCGTCCTCCTCCGCCGCC T C C20orf194 Ensembl:ENSG00000088854 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3407563..3407647 26863196 MeRIP-seq:(Medium) rs1468079915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92694,RMVar_hsa_circ_208432 78099 RMVar_ID_78099 Human_SNP_ID_671893057 m1A Human chr20 + 3407656 3407656 3407656 GCTCCACGCTAGCTGCGGCCGGGCGGGGCGGCAGGGCGTGCCGGGTGGGAGGGGGCGCGGCGCGC GCTCCACGCTAGCTGCGGCCGGGCGGGGCGGCCGGGCGTGCCGGGTGGGAGGGGGCGCGGCGCGC A C AL117334.2 Ensembl:ENSG00000288577 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:3407567..3407677 26863410 MeRIP-seq:(Medium) rs1439204511 Functional Loss SNV dbSNP153 33..33 33 - - - 78100 RMVar_ID_78100 Human_SNP_ID_671893058 m1A Human chr20 + 3407656 3407656 3407656 GCTCCACGCTAGCTGCGGCCGGGCGGGGCGGCAGGGCGTGCCGGGTGGGAGGGGGCGCGGCGCGC GCTCCACGCTAGCTGCGGCCGGGCGGGGCGGCGGGGCGTGCCGGGTGGGAGGGGGCGCGGCGCGC A G AL117334.2 Ensembl:ENSG00000288577 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:3407567..3407677 26863410 MeRIP-seq:(Medium) rs1439204511 Functional Loss SNV dbSNP153 33..33 33 - - - 78101 RMVar_ID_78101 Human_SNP_ID_671893117 m1A Human chr20 - 3407811 3407811 3407811 CGCGCTCCCAACATCCGGTCCGGCGGCCTCGCAGCTTAAGAAGTGGGGTCCCTGTGGCCGTGCGC CGCGCTCCCAACATCCGGTCCGGCGGCCTCGCTGCTTAAGAAGTGGGGTCCCTGTGGCCGTGCGC T A lnc-C20orf194-1 RNACentral:URS00008B519F lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3407723..3407855 32194978 MeRIP-seq:(Medium) rs1420587682 Functional Loss SNV dbSNP153 33..33 33 - - - 78102 RMVar_ID_78102 Human_SNP_ID_671909670 m1A Human chr20 - 3471079 3471079 3471079 CCATCTTCCCGGGGCTGAGACGGCGCCCCGCGAACACATACACACACACCGCACGGCCGGCTCCG CCATCTTCCCGGGGCTGAGACGGCGCCCCGCGGACACATACACACACACCGCACGGCCGGCTCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3471014..3471287 26863196 MeRIP-seq:(Medium) rs933545679 Functional Loss SNV dbSNP153 33..33 33 - - - 78103 RMVar_ID_78103 Human_SNP_ID_671909685 m1A Human chr20 + 3471096 3471096 3471096 TGTGTGTGTATGTGTTCGCGGGGCGCCGTCTCAGCCCCGGGAAGATGGTGGCTGCAGCGGCGGCA TGTGTGTGTATGTGTTCGCGGGGCGCCGTCTCGGCCCCGGGAAGATGGTGGCTGCAGCGGCGGCA A G ATRN Ensembl:ENSG00000088812 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3471051..3471250 26863196 MeRIP-seq:(Medium) rs1394641025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659201 RMVar_hsa_circ_98188,RMVar_hsa_circ_208453 78104 RMVar_ID_78104 Human_SNP_ID_671909732 m1A Human chr20 + 3471208 3471208 3471208 GGGCAGGAGCGGCGGGCCGCACTGGGACTGGGACGTGACCAGGGCTGGGAGGCCGGGGCTGGGGG GGGCAGGAGCGGCGGGCCGCACTGGGACTGGGTCGTGACCAGGGCTGGGAGGCCGGGGCTGGGGG A T ATRN Ensembl:ENSG00000088812 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3471077..3471250 26863196 MeRIP-seq:(Medium) rs1483832591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960564,Human_RBP_ID_4659203,Human_RBP_ID_22452872 RMVar_hsa_circ_98188,RMVar_hsa_circ_208453 78105 RMVar_ID_78105 Human_SNP_ID_671958589 m1A Human chr20 - 3670064 3670064 3670064 AGGGGAGAATGTTTTGAAGGAACATCACAGGAAATGACAAGGCCTTGGGGGATGGGATGGGGACA AGGGGAGAATGTTTTGAAGGAACATCACAGGAGATGACAAGGCCTTGGGGGATGGGATGGGGACA T C ADAM33 Ensembl:ENSG00000149451 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3670015..3670239 26863196 MeRIP-seq:(Medium) rs1342139164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110636,RMVar_hsa_circ_208488 78106 RMVar_ID_78106 Human_SNP_ID_671960015 m1A Human chr20 - 3673541 3673541 3673541 GTGAGCCCCGCGGGCGGGGGCGAGGGAGAGACAGGAGGCTCTACGGCCGCAGTGACCGCCCTCCC GTGAGCCCCGCGGGCGGGGGCGAGGGAGAGACTGGAGGCTCTACGGCCGCAGTGACCGCCCTCCC T A ADAM33 Ensembl:ENSG00000149451 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3673493..3673621 26863196 MeRIP-seq:(Medium) rs779520648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110636,RMVar_hsa_circ_208488,RMVar_hsa_circ_10445 78107 RMVar_ID_78107 Human_SNP_ID_671960501 m1A Human chr20 + 3674552 3674552 3674552 CCAGGAAGGCTGGTCATGCCCGCTTTGTTCCCAGGATCCCTGTGGCCACAGGTTCCTTTCCAGGT CCAGGAAGGCTGGTCATGCCCGCTTTGTTCCCGGGATCCCTGTGGCCACAGGTTCCTTTCCAGGT A G NONHSAG031158.2 RNACentral:URS00008C2953 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3674503..3674903 32194978 MeRIP-seq:(Medium) rs769864991 Functional Loss SNV dbSNP153 33..33 33 - - - 78108 RMVar_ID_78108 Human_SNP_ID_671960665 m1A Human chr20 + 3674934 3674934 3674934 GCAAGAGGGAGGGTGTGGTAGGGGCTGGCTCCAACCGCCCCTTAGGAATGCAAGGAGGAGTAGGG GCAAGAGGGAGGGTGTGGTAGGGGCTGGCTCCCACCGCCCCTTAGGAATGCAAGGAGGAGTAGGG A C NONHSAG031158.2 RNACentral:URS00008C2953 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3674902..3675049 26863196 MeRIP-seq:(Medium) rs749976121 Functional Loss SNV dbSNP153 33..33 33 - - - 78109 RMVar_ID_78109 Human_SNP_ID_671960708 m1A Human chr20 - 3675029 3675029 3675029 ATGGGCAGCCAGTGGTGCTGGCCCCCAACCACACGGTGAGATGCTTCCATGGGCTCTGGGATGCA ATGGGCAGCCAGTGGTGCTGGCCCCCAACCACGCGGTGAGATGCTTCCATGGGCTCTGGGATGCA T C ADAM33 Ensembl:ENSG00000149451 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3674917..3675048 26863196 MeRIP-seq:(Medium) rs780144529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2056810,Human_Splice_Rec_2056811,Human_Splice_Rec_2056852,Human_Splice_Rec_2056853,Human_Splice_Rec_2056888,Human_Splice_Rec_2056889,Human_Splice_Rec_2056928,Human_Splice_Rec_2056929,Human_Splice_Rec_2056970 78110 RMVar_ID_78110 Human_SNP_ID_671962083 m1A Human chr20 - 3679541 3679541 3679541 AGGACATATCCCTGGGCAGCCAGTCACCCCGCACTGGGTCCTGGATGGACAACCCTGGCGCACCG AGGACATATCCCTGGGCAGCCAGTCACCCCGCTCTGGGTCCTGGATGGACAACCCTGGCGCACCG T A ADAM33 Ensembl:ENSG00000149451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3679450..3679617 26863196 MeRIP-seq:(Medium) rs986191067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2056806,Human_Splice_Rec_2056807,Human_Splice_Rec_2056848,Human_Splice_Rec_2056849,Human_Splice_Rec_2056884,Human_Splice_Rec_2056885,Human_Splice_Rec_2056924,Human_Splice_Rec_2056925,Human_Splice_Rec_2056966,Human_Splice_Rec_2056967 78111 RMVar_ID_78111 Human_SNP_ID_671962084 m1A Human chr20 - 3679541 3679541 3679541 AGGACATATCCCTGGGCAGCCAGTCACCCCGCACTGGGTCCTGGATGGACAACCCTGGCGCACCG AGGACATATCCCTGGGCAGCCAGTCACCCCGCGCTGGGTCCTGGATGGACAACCCTGGCGCACCG T C ADAM33 Ensembl:ENSG00000149451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3679450..3679617 26863196 MeRIP-seq:(Medium) rs986191067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2056806,Human_Splice_Rec_2056807,Human_Splice_Rec_2056848,Human_Splice_Rec_2056849,Human_Splice_Rec_2056884,Human_Splice_Rec_2056885,Human_Splice_Rec_2056924,Human_Splice_Rec_2056925,Human_Splice_Rec_2056966,Human_Splice_Rec_2056967 78112 RMVar_ID_78112 Human_SNP_ID_671962904 m1A Human chr20 - 3681909 3681909 3681909 CTCTGGCCAGTGCCAGGCGCCGGGGTGCTTCAAGGTGAGGACGCGGGCGGGGTGCGCCCTGAGGG CTCTGGCCAGTGCCAGGCGCCGGGGTGCTTCAGGGTGAGGACGCGGGCGGGGTGCGCCCTGAGGG T C ADAM33 Ensembl:ENSG00000149451 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3679510..3681997 32194978 MeRIP-seq:(Medium) rs1173686783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2056805,Human_Splice_Rec_2056847,Human_Splice_Rec_2056883,Human_Splice_Rec_2056923,Human_Splice_Rec_2056965 78113 RMVar_ID_78113 Human_SNP_ID_671983256 m1A Human chr20 + 3753724 3753724 3753724 ACGACGCCACAGAGCCAGCTCCGTCCTCTCCCAGACCCTGGTGGGAGTCCCTGTGGCTTGGGGTG ACGACGCCACAGAGCCAGCTCCGTCCTCTCCCGGACCCTGGTGGGAGTCCCTGTGGCTTGGGGTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:3753576..3753975 26863196 MeRIP-seq:(Medium) rs1487085197 Functional Loss SNV dbSNP153 33..33 33 - - - 78114 RMVar_ID_78114 Human_SNP_ID_671983262 m1A Human chr20 - 3753739 3753739 3753739 GGGTCCCCCACTCCCCACCCCAAGCCACAGGGACTCCCACCAGGGTCTGGGAGAGGACGGAGCTG GGGTCCCCCACTCCCCACCCCAAGCCACAGGGTCTCCCACCAGGGTCTGGGAGAGGACGGAGCTG T A C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr20:3753576..3753999;chr20:3753645..3753800 26863196,26863410 MeRIP-seq:(Medium) rs9171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281405,Human_RBP_ID_5240032,Human_RBP_ID_9353995,Human_RBP_ID_18463244,Human_RBP_ID_26492858,Human_RBP_ID_27564524 Human_miRNA_ID_2210941 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 78115 RMVar_ID_78115 Human_SNP_ID_671983263 m1A Human chr20 - 3753739 3753739 3753739 GGGTCCCCCACTCCCCACCCCAAGCCACAGGGACTCCCACCAGGGTCTGGGAGAGGACGGAGCTG GGGTCCCCCACTCCCCACCCCAAGCCACAGGGGCTCCCACCAGGGTCTGGGAGAGGACGGAGCTG T C C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr20:3753576..3753999;chr20:3753645..3753800 26863196,26863410 MeRIP-seq:(Medium) rs9171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281405,Human_RBP_ID_5240032,Human_RBP_ID_9353995,Human_RBP_ID_18463244,Human_RBP_ID_26492858,Human_RBP_ID_27564524 Human_miRNA_ID_2210941 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 78116 RMVar_ID_78116 Human_SNP_ID_671983282 m1A Human chr20 - 3753812 3753812 3753812 AGTCTCCTGCCGGAAGAAATGGGTTGAGCCCGAAAGGAGGCTGTCTGAGGAAGGGAGAGGGAGGG AGTCTCCTGCCGGAAGAAATGGGTTGAGCCCGGAAGGAGGCTGTCTGAGGAAGGGAGAGGGAGGG T C C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3753762..3754000 26863196 MeRIP-seq:(Medium) rs1380937595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563820,Human_RBP_ID_3648447,Human_RBP_ID_5118813,Human_RBP_ID_9353997,Human_RBP_ID_17658958,Human_RBP_ID_17700455,Human_RBP_ID_17971488,Human_RBP_ID_23904655,Human_RBP_ID_26493353 Human_miRNA_ID_1200903,Human_miRNA_ID_2580049,Human_miRNA_ID_2999909 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 78117 RMVar_ID_78117 Human_SNP_ID_671983301 m1A Human chr20 - 3753867 3753867 3753867 GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCACTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCTCTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC T A C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2295340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563821,Human_RBP_ID_5119136,Human_RBP_ID_5147847,Human_RBP_ID_5503335,Human_RBP_ID_17658959,Human_RBP_ID_18950198,Human_RBP_ID_22081242,Human_RBP_ID_23184179,Human_RBP_ID_26490332,Human_RBP_ID_27296836,Human_RBP_ID_27485642 Human_miRNA_ID_1340288,Human_miRNA_ID_3078934 GWAS_ID_9324 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 78118 RMVar_ID_78118 Human_SNP_ID_671983302 m1A Human chr20 - 3753867 3753867 3753867 GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCACTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCGCTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC T C C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2295340 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_563821,Human_RBP_ID_5119136,Human_RBP_ID_5147847,Human_RBP_ID_5503335,Human_RBP_ID_17658959,Human_RBP_ID_18950198,Human_RBP_ID_22081242,Human_RBP_ID_23184179,Human_RBP_ID_26490332,Human_RBP_ID_27296836,Human_RBP_ID_27485642 Human_miRNA_ID_1340288,Human_miRNA_ID_3078934 GWAS_ID_9324 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 78119 RMVar_ID_78119 Human_SNP_ID_671983308 m1A Human chr20 + 3753886 3753886 3753886 AGAGAGGAGGAAGTGGGAGAGGAGGACGAGGGAGGGGCAGGGTGGCAGCACAAATGAAGGCAGAG AGAGAGGAGGAAGTGGGAGAGGAGGACGAGGGGGGGGCAGGGTGGCAGCACAAATGAAGGCAGAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3753601..3754091 26863196 MeRIP-seq:(Medium) rs184545783 Functional Loss SNV dbSNP153 33..33 33 - - - 78120 RMVar_ID_78120 Human_SNP_ID_671983309 m1A Human chr20 + 3753886 3753886 3753886 AGAGAGGAGGAAGTGGGAGAGGAGGACGAGGGAGGGGCAGGGTGGCAGCACAAATGAAGGCAGAG AGAGAGGAGGAAGTGGGAGAGGAGGACGAGGGTGGGGCAGGGTGGCAGCACAAATGAAGGCAGAG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:3753601..3754091 26863196 MeRIP-seq:(Medium) rs184545783 Functional Loss SNV dbSNP153 33..33 33 - - - 78121 RMVar_ID_78121 Human_SNP_ID_671984775 m1A Human chr20 - 3758627 3758627 3758627 GAGTATCCGCTTTGCGGCAGGCCACGATGCAGAAGGATCCCACAGCCACGTCCACTTTGATGAGA GAGTATCCGCTTTGCGGCAGGCCACGATGCAGGAGGATCCCACAGCCACGTCCACTTTGATGAGA T C C20orf27 Ensembl:ENSG00000101220 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3758576..3758734 26863196 MeRIP-seq:(Medium) rs920160078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1596975,Human_RBP_ID_1929642,Human_RBP_ID_3648454,Human_RBP_ID_4663497,Human_RBP_ID_9117051 Human_Splice_Rec_2057075,Human_Splice_Rec_2057082,Human_Splice_Rec_2057083,Human_Splice_Rec_2057092,Human_Splice_Rec_2057093,Human_Splice_Rec_2057102,Human_Splice_Rec_2057103 RMVar_hsa_circ_114478,RMVar_hsa_circ_208494,RMVar_hsa_circ_104708,RMVar_hsa_circ_208495,RMVar_hsa_circ_297004 78122 RMVar_ID_78122 Human_SNP_ID_671987017 m1A Human chr20 + 3767710 3767710 3767710 CCGGGGCCGGGGAGGGCAGGGACGACCACTGCAGCGGCGGCGGCTGCAGGAGCTCAACGCCGAGC CCGGGGCCGGGGAGGGCAGGGACGACCACTGCCGCGGCGGCGGCTGCAGGAGCTCAACGCCGAGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3767595..3767775 26863196 MeRIP-seq:(Medium) rs1444341004 Functional Loss SNV dbSNP153 33..33 33 - - - 78123 RMVar_ID_78123 Human_SNP_ID_671991522 m1A Human chr20 - 3784202 3784202 3784202 TGCAAGGCTGGCAGCCCCCACCCCCACCCCCCAGGCCGCCTTGAGAAGCACAGTTTAACTCACTG TGCAAGGCTGGCAGCCCCCACCCCCACCCCCCCGGCCGCCTTGAGAAGCACAGTTTAACTCACTG T G CENPB Ensembl:ENSG00000125817 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs928826845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563889,Human_RBP_ID_23904922 78124 RMVar_ID_78124 Human_SNP_ID_671991530 m1A Human chr20 + 3784226 3784226 3784226 AGGCGGCCTGGGGGGTGGGGGTGGGGGCTGCCAGCCTTGCAGGGGGCCTAGGCTGGACCTTCTTC AGGCGGCCTGGGGGGTGGGGGTGGGGGCTGCCCGCCTTGCAGGGGGCCTAGGCTGGACCTTCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:3784176..3784667 26863196 MeRIP-seq:(Medium) rs1463659866 Functional Loss SNV dbSNP153 33..33 33 - - - 78125 RMVar_ID_78125 Human_SNP_ID_671991757 m1A Human chr20 - 3784994 3784994 3784994 CTTCGGGGCTTATGGTGCCCAGGAGGAAGCCCAGTGCCCTACTCTGCATTTCCTGGAAGGTGGGG CTTCGGGGCTTATGGTGCCCAGGAGGAAGCCCGGTGCCCTACTCTGCATTTCCTGGAAGGTGGGG T C CENPB Ensembl:ENSG00000125817 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3784946..3785096 32194978 MeRIP-seq:(Medium) rs748676791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563905,Human_RBP_ID_2685040,Human_RBP_ID_5148019,Human_RBP_ID_8857301,Human_RBP_ID_17511563,Human_RBP_ID_23904930,Human_RBP_ID_27296905 RMVar_hsa_circ_208497 78126 RMVar_ID_78126 Human_SNP_ID_671991786 m1A Human chr20 + 3785065 3785065 3785065 CCGGCCTCCACTACTCCCTGGGCCCAGTCCTCAGCCTCCAAGCCCTCCGAGGAGCTCTCCTCATC CCGGCCTCCACTACTCCCTGGGCCCAGTCCTCCGCCTCCAAGCCCTCCGAGGAGCTCTCCTCATC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:3784962..3785200 26863196 MeRIP-seq:(Medium) rs779148447 Functional Loss SNV dbSNP153 33..33 33 - - - 78127 RMVar_ID_78127 Human_SNP_ID_671991789 m1A Human chr20 - 3785069 3785069 3785069 GGAAGATGAGGAGAGCTCCTCGGAGGGCTTGGAGGCTGAGGACTGGGCCCAGGGAGTAGTGGAGG GGAAGATGAGGAGAGCTCCTCGGAGGGCTTGGTGGCTGAGGACTGGGCCCAGGGAGTAGTGGAGG T A CENPB Ensembl:ENSG00000125817 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:3784851..3785375;chr20:3783972..3785592;chr20:3784795..3785445;chr20:3784826..3785465 26863196 MeRIP-seq:(Medium) rs1041906979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206539,Human_RBP_ID_924778,Human_RBP_ID_1068238,Human_RBP_ID_3960040,Human_RBP_ID_5147849,Human_RBP_ID_5322848,Human_RBP_ID_8204806,Human_RBP_ID_8854672,Human_RBP_ID_8942864,Human_RBP_ID_9298581,Human_RBP_ID_9331761,Human_RBP_ID_9388567,Human_RBP_ID_9430645,Human_RBP_ID_14105260,Human_RBP_ID_17208214,Human_RBP_ID_17976437,Human_RBP_ID_22081534,Human_RBP_ID_23004832,Human_RBP_ID_23119578,Human_RBP_ID_24546712,Human_RBP_ID_26342670,Human_RBP_ID_26492860,Human_RBP_ID_26770605,Human_RBP_ID_27819549 RMVar_hsa_circ_208497 78128 RMVar_ID_78128 Human_SNP_ID_671991871 m1A Human chr20 - 3785186 3785186 3785186 AGAGGAAGAGGAGGAGGAAGGGGAGGAGGAGGAGGAGGAAGGGGGGGAAGGAGAGGAATTGGGGG AGAGGAAGAGGAGGAGGAAGGGGAGGAGGAGGCGGAGGAAGGGGGGGAAGGAGAGGAATTGGGGG T G CENPB Ensembl:ENSG00000125817 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:3785101..3785185 26863410 MeRIP-seq:(Medium) rs1328003800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17068989 78129 RMVar_ID_78129 Human_SNP_ID_671992193 m1A Human chr20 + 3785876 3785876 3785876 CTCCGCACAGCCCCGCGGCCTGGTCGGGCAGGAAGTCGTACCATAGACTGGTCTCGGTGGCGCTG CTCCGCACAGCCCCGCGGCCTGGTCGGGCAGGTAGTCGTACCATAGACTGGTCTCGGTGGCGCTG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr20:3785851..3785875;chr20:3785670..3785927 26863196 MeRIP-seq:(Medium) rs369656252 Functional Loss SNV dbSNP153 33..33 33 - - - 78130 RMVar_ID_78130 Human_SNP_ID_671992392 m1A Human chr20 - 3786466 3786466 3786466 GGGGGGCGCGCCGGGATGGGCCCCAAGAGGCGACAGCTGACGTTCCGGGAGAAGTCACGGATCAT GGGGGGCGCGCCGGGATGGGCCCCAAGAGGCGGCAGCTGACGTTCCGGGAGAAGTCACGGATCAT T C CENPB Ensembl:ENSG00000125817 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:3786351..3786775 26863196 MeRIP-seq:(Medium) rs1267994627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244834,Human_RBP_ID_4659638,Human_RBP_ID_22453291 78131 RMVar_ID_78131 Human_SNP_ID_671995049 m1A Human chr20 - 3796360 3796360 3796360 GGCCAGGCGCGAGGGAGGAGAGGGATGCGGGGAGGGCGGGGGGCGAGGGACGCCGGGCTCAGGCA GGCCAGGCGCGAGGGAGGAGAGGGATGCGGGGGGGGCGGGGGGCGAGGGACGCCGGGCTCAGGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3796310..3796388 26863196 MeRIP-seq:(Medium) rs1490318800 Functional Loss SNV dbSNP153 33..33 33 - - - 78132 RMVar_ID_78132 Human_SNP_ID_671995069 m1A Human chr20 - 3796406 3796406 3796406 CGAGGGGTGGGGGGGGGGGGAAGGAGGGAGGGAGGAAGAGCCACAGGGCCAGGCGCGAGGGAGGA CGAGGGGTGGGGGGGGGGGGAAGGAGGGAGGGGGGAAGAGCCACAGGGCCAGGCGCGAGGGAGGA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:3796318..3796406 26863410 MeRIP-seq:(Medium) rs1378387758 Functional Loss SNV dbSNP153 33..33 33 - - - 78133 RMVar_ID_78133 Human_SNP_ID_671995070 m1A Human chr20 - 3796418 3796409 3796418 GGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAGGAGGGAGGGAGGAAGAGCCACAGGGCCAGG GGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGG_________GGGAGGAAGAGCCACAGGGCCAGG CTCCCTCCTT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:3796336..3796419 26863410 MeRIP-seq:(Medium) rs1409058040 Functional Loss DEL dbSNP153 33..41 33 - - - 78134 RMVar_ID_78134 Human_SNP_ID_671995077 m1A Human chr20 - 3796418 3796418 3796418 GGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAGGAGGGAGGGAGGAAGAGCCACAGGGCCAGG GGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGGGAGGAGGGAGGGAGGAAGAGCCACAGGGCCAGG T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:3796336..3796419 26863410 MeRIP-seq:(Medium) rs1237307821 Functional Loss SNV dbSNP153 33..33 33 - - - 78135 RMVar_ID_78135 Human_SNP_ID_671995138 m1A Human chr20 - 3796448 3796448 3796448 ACAAACGCCGGCACAGCTGGCTGGGCCGAGGGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAG ACAAACGCCGGCACAGCTGGCTGGGCCGAGGGGGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:3796346..3796550 26863410 MeRIP-seq:(Medium) rs1371015271 Functional Loss SNV dbSNP153 33..33 33 - - - 78136 RMVar_ID_78136 Human_SNP_ID_671995139 m1A Human chr20 - 3796448 3796448 3796448 ACAAACGCCGGCACAGCTGGCTGGGCCGAGGGAGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAG ACAAACGCCGGCACAGCTGGCTGGGCCGAGGGCGGCAGCGGGCGAGGGGTGGGGGGGGGGGGAAG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:3796346..3796550 26863410 MeRIP-seq:(Medium) rs1371015271 Functional Loss SNV dbSNP153 33..33 33 - - - 78137 RMVar_ID_78137 Human_SNP_ID_671995146 m1A Human chr20 + 3796459 3796459 3796459 CCCCACCCCTCGCCCGCTGCCTCCCTCGGCCCAGCCAGCTGTGCCGGCGTTTGTTGGCTGCCCTG CCCCACCCCTCGCCCGCTGCCTCCCTCGGCCCCGCCAGCTGTGCCGGCGTTTGTTGGCTGCCCTG A C CDC25B Ensembl:ENSG00000101224 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:3796368..3796547 26863196 MeRIP-seq:(Medium) rs1448271735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132077,Human_RBP_ID_5472206,Human_RBP_ID_17086412,Human_RBP_ID_17658961,Human_RBP_ID_18951155,Human_RBP_ID_22600811 RMVar_hsa_circ_94429,RMVar_hsa_circ_208498 78138 RMVar_ID_78138 Human_SNP_ID_671995239 m1A Human chr20 + 3796697 3796697 3796697 GGGCGGCCGCTTCCTCGCCGGTCACCACCCTCACCCAGACCATGCACGACCTCGCCGGGCTCGGC GGGCGGCCGCTTCCTCGCCGGTCACCACCCTCGCCCAGACCATGCACGACCTCGCCGGGCTCGGC A G CDC25B Ensembl:ENSG00000101224 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:3796326..3797650 26863196 MeRIP-seq:(Medium) rs780219390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244255,Human_RBP_ID_27485769 Human_Splice_Rec_2057227,Human_Splice_Rec_2057257,Human_Splice_Rec_2057287 RMVar_hsa_circ_94429,RMVar_hsa_circ_208498 78139 RMVar_ID_78139 Human_SNP_ID_671996211 m1A Human chr20 - 3799601 3799601 3799601 CAGGCAAGGAATTCCAACACATGTTCCCTCTGAGGCCCCGCCCCCTCAGCCGTGTTACAGGAGAC CAGGCAAGGAATTCCAACACATGTTCCCTCTGGGGCCCCGCCCCCTCAGCCGTGTTACAGGAGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:3799589..3799731;chr20:3799599..3799830 26863196 MeRIP-seq:(Medium) rs974736045 Functional Loss SNV dbSNP153 33..33 33 - - - 78140 RMVar_ID_78140 Human_SNP_ID_671996423 m1A Human chr20 + 3800305 3800305 3800305 CCTTCTCTGTCCTAGGTTTGAACAGGCCATCCAGGCAGCCAGCCGGATCATTCGAAAGTAAGTGT CCTTCTCTGTCCTAGGTTTGAACAGGCCATCCGGGCAGCCAGCCGGATCATTCGAAAGTAAGTGT A G CDC25B Ensembl:ENSG00000101224 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:3800276..3800350 26863196 MeRIP-seq:(Medium) rs1347673573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960042,Human_RBP_ID_5132079,Human_RBP_ID_17971612,Human_RBP_ID_21983311,Human_RBP_ID_22670679 Human_Splice_Rec_2057144,Human_Splice_Rec_2057145,Human_Splice_Rec_2057172,Human_Splice_Rec_2057173,Human_Splice_Rec_2057202,Human_Splice_Rec_2057203,Human_Splice_Rec_2057232,Human_Splice_Rec_2057233,Human_Splice_Rec_2057262,Human_Splice_Rec_2057263,Human_Splice_Rec_2057292,Human_Splice_Rec_2057293 Human_miRNA_ID_2333442,Human_miRNA_ID_2966526 RMVar_hsa_circ_44790,RMVar_hsa_circ_94429,RMVar_hsa_circ_208498 78141 RMVar_ID_78141 Human_SNP_ID_671996706 m1A Human chr20 - 3801024 3801024 3801024 GCTTCCCTGCGGCTGGCCCACTCTGCCAGAGCATGGGTGGAGCTGGGATGTGTGGGCTTCCATGG GCTTCCCTGCGGCTGGCCCACTCTGCCAGAGCGTGGGTGGAGCTGGGATGTGTGGGCTTCCATGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:3801001..3801025 26863196 MeRIP-seq:(Medium) rs1281547803 Functional Loss SNV dbSNP153 33..33 33 - - - 78142 RMVar_ID_78142 Human_SNP_ID_671998086 m1A Human chr20 + 3805452 3805452 3805452 CTAATCTCTGTAGGAACCGTGGTATGTCTGCCATGTTGCCCCTTTCTCTTTTCCCCTTTCCTGTC CTAATCTCTGTAGGAACCGTGGTATGTCTGCCCTGTTGCCCCTTTCTCTTTTCCCCTTTCCTGTC A C CDC25B Ensembl:ENSG00000101224 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:3805401..3805475 32194978 MeRIP-seq:(Medium) rs928535791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563956,Human_RBP_ID_3648579,Human_RBP_ID_18950204,Human_RBP_ID_23904998,Human_RBP_ID_25611551 Human_miRNA_ID_421369 RMVar_hsa_circ_77977,RMVar_hsa_circ_208501,RMVar_hsa_circ_208503,RMVar_hsa_circ_90004 78143 RMVar_ID_78143 Human_SNP_ID_671998087 m1A Human chr20 + 3805452 3805452 3805452 CTAATCTCTGTAGGAACCGTGGTATGTCTGCCATGTTGCCCCTTTCTCTTTTCCCCTTTCCTGTC CTAATCTCTGTAGGAACCGTGGTATGTCTGCCTTGTTGCCCCTTTCTCTTTTCCCCTTTCCTGTC A T CDC25B Ensembl:ENSG00000101224 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:3805401..3805475 32194978 MeRIP-seq:(Medium) rs928535791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563956,Human_RBP_ID_3648579,Human_RBP_ID_18950204,Human_RBP_ID_23904998,Human_RBP_ID_25611551 Human_miRNA_ID_421369 RMVar_hsa_circ_77977,RMVar_hsa_circ_208501,RMVar_hsa_circ_208503,RMVar_hsa_circ_90004 78144 RMVar_ID_78144 Human_SNP_ID_672002396 m1A Human chr20 + 3820636 3820636 3820636 CGGACGGAAGGCTGAGGCGACGCCTCGACGACAGCGGACCGGAGCTGCAGGGGCAACACATTCAG CGGACGGAAGGCTGAGGCGACGCCTCGACGACGGCGGACCGGAGCTGCAGGGGCAACACATTCAG A G AL109804.1,AP5S1 Ensembl:ENSG00000274949,Ensembl:ENSG00000125843 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:3820586..3820694 26863196 MeRIP-seq:(Medium) rs1441570502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659641,Human_RBP_ID_7023302,Human_RBP_ID_18422807,Human_RBP_ID_23005088 Human_Splice_Rec_2057363 Human_miRNA_ID_2014098,Human_miRNA_ID_2760497 RMVar_hsa_circ_127138,RMVar_hsa_circ_208505 78145 RMVar_ID_78145 Human_SNP_ID_672003745 m1A Human chr20 + 3824811 3824811 3824811 AAAAATTAGCTGGGTGTATGGCGCCCACCTGTAATCCTAGCTGCTCAGGGGGCTGAGTCATGGGA AAAAATTAGCTGGGTGTATGGCGCCCACCTGTGATCCTAGCTGCTCAGGGGGCTGAGTCATGGGA A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11554187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1973926,Human_miRNA_ID_1976105,Human_miRNA_ID_2891297 RMVar_hsa_circ_127138,RMVar_hsa_circ_208505,RMVar_hsa_circ_80302,RMVar_hsa_circ_208507 78146 RMVar_ID_78146 Human_SNP_ID_672015235 m1A Human chr20 - 3862225 3862225 3862225 AATTCTGCAATGAGGGAAAATATGAATAAGGCAGTTGCCTCTCCCAAGAGCTCACAAAGGGCAGC AATTCTGCAATGAGGGAAAATATGAATAAGGCTGTTGCCTCTCCCAAGAGCTCACAAAGGGCAGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3862223..3862342 26863196 MeRIP-seq:(Medium) rs776168161 Functional Loss SNV dbSNP153 33..33 33 - - - 78147 RMVar_ID_78147 Human_SNP_ID_672016332 m1A Human chr20 - 3866176 3866176 3866176 GAGGGGCCAGGTGTACTGCAGGAACGGAACAGATGGGTGGTGGGAAGAGCCCAGGGCTTCACTAG GAGGGGCCAGGTGTACTGCAGGAACGGAACAGGTGGGTGGTGGGAAGAGCCCAGGGCTTCACTAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3866126..3866175 32194978 MeRIP-seq:(Medium) rs1215649494 Functional Loss SNV dbSNP153 33..33 33 - - - 78148 RMVar_ID_78148 Human_SNP_ID_672017648 m1A Human chr20 + 3870998 3870998 3870998 CGCCTCCCAGGTTCAAGTGATTCTCCTGCTTCAGCCTCTCAAGTAGCTGGGATTACAGATGCCCG CGCCTCCCAGGTTCAAGTGATTCTCCTGCTTCGGCCTCTCAAGTAGCTGGGATTACAGATGCCCG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1271352646 Functional Loss SNV dbSNP153 33..33 33 - - - 78149 RMVar_ID_78149 Human_SNP_ID_672017927 m1A Human chr20 + 3872176 3872176 3872176 TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCATACCTATAATCCCAGCACTTTGGGAGACCAAG TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCCTACCTATAATCCCAGCACTTTGGGAGACCAAG A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs902921717 Functional Loss SNV dbSNP153 33..33 33 - - - 78150 RMVar_ID_78150 Human_SNP_ID_672017928 m1A Human chr20 + 3872176 3872176 3872176 TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCATACCTATAATCCCAGCACTTTGGGAGACCAAG TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCTTACCTATAATCCCAGCACTTTGGGAGACCAAG A T MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs902921717 Functional Loss SNV dbSNP153 33..33 33 - - - 78151 RMVar_ID_78151 Human_SNP_ID_672018191 m1A Human chr20 + 3873459 3873459 3873459 GGGAGGCTGAGACAGGAGAATAGCTTGAACCCAGTAGGTGGAGATTTCAGTGAGCCGAGATCGTG GGGAGGCTGAGACAGGAGAATAGCTTGAACCCGGTAGGTGGAGATTTCAGTGAGCCGAGATCGTG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs891149569 Functional Loss SNV dbSNP153 33..33 33 - - - 78152 RMVar_ID_78152 Human_SNP_ID_672028824 m1A Human chr20 + 3907933 3907933 3907933 TGACTTATTTTTCTTCCCCATTTAGTTTTTCCATGGTTTGGACTGGATATCGGTGGAACTCTGGT TGACTTATTTTTCTTCCCCATTTAGTTTTTCCCTGGTTTGGACTGGATATCGGTGGAACTCTGGT A C PANK2 Ensembl:ENSG00000125779 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3907926..3908000 32194978 MeRIP-seq:(Medium) rs752528898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923848,Human_RBP_ID_1597154,Human_RBP_ID_14106647,Human_RBP_ID_18773126,Human_RBP_ID_22670685,Human_RBP_ID_23002190,Human_RBP_ID_24560702,Human_RBP_ID_25626744 Human_Splice_Rec_2057400,Human_Splice_Rec_2057412,Human_Splice_Rec_2057420,Human_Splice_Rec_2057436,Human_Splice_Rec_2057446,Human_Splice_Rec_2057456,Human_Splice_Rec_2057470,Human_Splice_Rec_2057482,Human_Splice_Rec_2057494 Human_miRNA_ID_2657800 RMVar_hsa_circ_208517,RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_272036,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339,RMVar_hsa_circ_287845,RMVar_hsa_circ_317527,RMVar_hsa_circ_276161,RMVar_hsa_circ_208519,RMVar_hsa_circ_208520,RMVar_hsa_circ_208518 78153 RMVar_ID_78153 Human_SNP_ID_672091502 m1A Human chr20 - 4152040 4152040 4152040 ACATCCCATTGGCGCCCTTAGATTCTTGCAGCAATCTGCACAGTTGCTTTTGTGGAAAGAAAATA ACATCCCATTGGCGCCCTTAGATTCTTGCAGCTATCTGCACAGTTGCTTTTGTGGAAAGAAAATA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:4152038..4152151 26863196 MeRIP-seq:(Medium) rs1568727640 Functional Loss SNV dbSNP153 33..33 33 - - - 78154 RMVar_ID_78154 Human_SNP_ID_672092707 m1A Human chr20 - 4157285 4157285 4157285 CCCTCCCCAGGGTCCCTCCTCCAGCCATGTCAAATCCAGTAGTAAGAGCAGCCAACCGGTATTAG CCCTCCCCAGGGTCCCTCCTCCAGCCATGTCAGATCCAGTAGTAAGAGCAGCCAACCGGTATTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:4157283..4157656 26863196 MeRIP-seq:(Medium) rs970500306 Functional Loss SNV dbSNP153 33..33 33 - - - 78155 RMVar_ID_78155 Human_SNP_ID_672092712 m1A Human chr20 + 4157314 4157314 4157314 GATTTGACATGGCTGGAGGAGGGACCCTGGGGAGGGCCCTGTCATCGTGGACATGAGGGAAGAAA GATTTGACATGGCTGGAGGAGGGACCCTGGGGGGGGCCCTGTCATCGTGGACATGAGGGAAGAAA A G SMOX Ensembl:ENSG00000088826 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:4157310..4157633 26863196 MeRIP-seq:(Medium) rs1197221733 Functional Loss SNV dbSNP153 33..33 33 - - - 78156 RMVar_ID_78156 Human_SNP_ID_672099037 m1A Human chr20 + 4182405 4182405 4182405 GGAGCCCCGGGGGGGCAGGTGGGATGAGGATGAGCAGTGGTCGGTGGTGGTGGAGTGCGAGGACT GGAGCCCCGGGGGGGCAGGTGGGATGAGGATGGGCAGTGGTCGGTGGTGGTGGAGTGCGAGGACT A G SMOX Ensembl:ENSG00000088826 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:4182141..4182537 26863196 MeRIP-seq:(Medium) rs1173416133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831253,Human_RBP_ID_924319,Human_RBP_ID_5383304,Human_RBP_ID_9431472,Human_RBP_ID_24553412,Human_RBP_ID_26788122 RMVar_hsa_circ_9060,RMVar_hsa_circ_17617 78157 RMVar_ID_78157 Human_SNP_ID_672099448 m1A Human chr20 + 4183620 4183620 4183620 CTCCAGCGGGGCGGATGTGGAGAAGCTGGCCAAGCCCCTGCCGTACACAGAGAGCTCAAAGACAG CTCCAGCGGGGCGGATGTGGAGAAGCTGGCCAGGCCCCTGCCGTACACAGAGAGCTCAAAGACAG A G SMOX Ensembl:ENSG00000088826 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:4183572..4186761 32194978 MeRIP-seq:(Medium) rs749842121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2057559,Human_Splice_Rec_2057575,Human_Splice_Rec_2057589,Human_Splice_Rec_2057603,Human_Splice_Rec_2057629,Human_Splice_Rec_2057637,Human_Splice_Rec_2057643,Human_Splice_Rec_2057649 RMVar_hsa_circ_9060,RMVar_hsa_circ_17617 78158 RMVar_ID_78158 Human_SNP_ID_672107607 m1A Human chr20 + 4217537 4217537 4217537 ACTGTGTGAAGAGTTGAGAAAAAGAGGAATAAAACCCTAGGGAGCATTTAAGAGTGGAGAGAGAA ACTGTGTGAAGAGTTGAGAAAAAGAGGAATAACACCCTAGGGAGCATTTAAGAGTGGAGAGAGAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:4217447..4217848 26863196 MeRIP-seq:(Medium) rs1022092749 Functional Loss SNV dbSNP153 33..33 33 - - - 78159 RMVar_ID_78159 Human_SNP_ID_672107619 m1A Human chr20 + 4217587 4217584 4217588 AGAGTGGAGAGAGAAGGCTGTGGAGGAGGCAGAGAGAGAGTAGGGTCAGCAGGTCAGAAGAGATC AGAGTGGAGAGAGAAGGCTGTGGAGGAGGC____AGAGAGTAGGGTCAGCAGGTCAGAAGAGATC CAGAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:4217521..4217641 26863196 MeRIP-seq:(Medium) rs960340574 Functional Loss DEL dbSNP153 31..34 33 - - - 78160 RMVar_ID_78160 Human_SNP_ID_672207758 m1A Human chr20 - 4629591 4629591 4629591 AGAGGCACCCTGGATCTCTTGACGTGGTTCACATGAAAGATGCCAATGGCAACAGCTTTGCCACT AGAGGCACCCTGGATCTCTTGACGTGGTTCACGTGAAAGATGCCAATGGCAACAGCTTTGCCACT T C RPS4XP2 Ensembl:ENSG00000226948 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1195082649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9117663 78161 RMVar_ID_78161 Human_SNP_ID_672207759 m1A Human chr20 - 4629591 4629591 4629591 AGAGGCACCCTGGATCTCTTGACGTGGTTCACATGAAAGATGCCAATGGCAACAGCTTTGCCACT AGAGGCACCCTGGATCTCTTGACGTGGTTCACCTGAAAGATGCCAATGGCAACAGCTTTGCCACT T G RPS4XP2 Ensembl:ENSG00000226948 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1195082649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9117663 78162 RMVar_ID_78162 Human_SNP_ID_672224152 m1A Human chr20 + 4699331 4699331 4699331 AAGCCTGGAGGATGGAACACTGGGGGCAGCCGATACCCGGGGCAGGGCAGCCCTGGAGGCAACCG AAGCCTGGAGGATGGAACACTGGGGGCAGCCGCTACCCGGGGCAGGGCAGCCCTGGAGGCAACCG A C PRNP Ensembl:ENSG00000171867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:4699281..4699728 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_831519,Human_RBP_ID_4650771,Human_RBP_ID_9354000,Human_RBP_ID_22452883,Human_RBP_ID_27486602 Human_miRNA_ID_2152385,Human_miRNA_ID_2381604,Human_miRNA_ID_2420847,Human_miRNA_ID_3024614,Human_miRNA_ID_3091341 RMVar_hsa_circ_94105,RMVar_hsa_circ_208542,RMVar_hsa_circ_85307,RMVar_hsa_circ_208541 78163 RMVar_ID_78163 Human_SNP_ID_672224194 m1A Human chr20 - 4699409 4699409 4699409 CCCCAGCCACCACCATGAGGCTGCCCCCAGCCACCACCATGAGGCTGCCCCCAGCCACCACCGCC CCCCAGCCACCACCATGAGGCTGCCCCCAGCCTCCACCATGAGGCTGCCCCCAGCCACCACCGCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:4699201..4699846 26863196 MeRIP-seq:(Medium) rs767207185 Functional Loss SNV dbSNP153 33..33 33 - - - 78164 RMVar_ID_78164 Human_SNP_ID_672224269 m1A Human chr20 - 4699574 4699561 4699574 ATGTAGCCGCCAAGGCCCCCCACCACTGCCCCAGCTGCTGCAGCACCAGCCATGTGCTTCATGTT ATGTAGCCGCCAAGGCCCCCCACCACTGCCCC_____________CCAGCCATGTGCTTCATGTT GTGCTGCAGCAGCT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:4699526..4699775 32194978 MeRIP-seq:(Medium) rs1476694110 Functional Loss DEL dbSNP153 33..45 33 - - - 78165 RMVar_ID_78165 Human_SNP_ID_672224292 m1A Human chr20 + 4699613 4699613 4699613 GTGGTGGGGGGCCTTGGCGGCTACATGCTGGGAAGTGCCATGAGCAGGCCCATCATACATTTCGG GTGGTGGGGGGCCTTGGCGGCTACATGCTGGGGAGTGCCATGAGCAGGCCCATCATACATTTCGG A G PRNP Ensembl:ENSG00000171867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:4699230..4699624 32194978 MeRIP-seq:(Medium) rs772735889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244601,Human_RBP_ID_779238,Human_RBP_ID_9354002,Human_RBP_ID_18471236,Human_RBP_ID_22452885,Human_RBP_ID_22766920 Human_miRNA_ID_421372,Human_miRNA_ID_2134663 RMVar_hsa_circ_94105,RMVar_hsa_circ_99728,RMVar_hsa_circ_208542,RMVar_hsa_circ_85307,RMVar_hsa_circ_208541,RMVar_hsa_circ_208543 78166 RMVar_ID_78166 Human_SNP_ID_672224410 m1A Human chr20 + 4699870 4699870 4699870 GGAGCGCGTGGTTGAGCAGATGTGTATCACCCAGTACGAGAGGGAATCTCAGGCCTATTACCAGA GGAGCGCGTGGTTGAGCAGATGTGTATCACCCGGTACGAGAGGGAATCTCAGGCCTATTACCAGA A G PRNP Ensembl:ENSG00000171867 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:4699820..4700116 32194978 MeRIP-seq:(Medium) rs74315406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779239,Human_RBP_ID_9117713,Human_RBP_ID_17976668,Human_RBP_ID_22395270,Human_RBP_ID_22766922,Human_RBP_ID_26821204 Human_miRNA_ID_2956581 Clinvar_Rec_359 GWAS_ID_9325,GWAS_ID_9326,GWAS_ID_9327,GWAS_ID_9328 RMVar_hsa_circ_94105,RMVar_hsa_circ_99728,RMVar_hsa_circ_208542,RMVar_hsa_circ_85307,RMVar_hsa_circ_208541,RMVar_hsa_circ_208543 78167 RMVar_ID_78167 Human_SNP_ID_672282046 m1A Human chr20 + 4925616 4925616 4925616 GTAAGCACCCTAACTTGCCTTCCTATCTCCAGACCCTTCCTGCCCCGGCACCCACCGCAGGAATT GTAAGCACCCTAACTTGCCTTCCTATCTCCAGTCCCTTCCTGCCCCGGCACCCACCGCAGGAATT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:4925612..4925723 26863196 MeRIP-seq:(Medium) rs1425841889 Functional Loss SNV dbSNP153 33..33 33 - - - 78168 RMVar_ID_78168 Human_SNP_ID_672301147 m1A Human chr20 - 5001472 5001472 5001472 TTGCAGGCGGCTGTCGCGGGGACCGGAGGCGGAGGCTGCAGCGGGCACTGCGGCGCCGAGGCGCG TTGCAGGCGGCTGTCGCGGGGACCGGAGGCGGCGGCTGCAGCGGGCACTGCGGCGCCGAGGCGCG T G SLC23A2 Ensembl:ENSG00000089057 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs113708270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244185,Human_RBP_ID_4659231,Human_RBP_ID_18422811 Human_Splice_Rec_2057781 RMVar_hsa_circ_123079,RMVar_hsa_circ_208555,RMVar_hsa_circ_124520,RMVar_hsa_circ_208561 78169 RMVar_ID_78169 Human_SNP_ID_672329585 m1A Human chr20 - 5106269 5106269 5106269 ACCCCTCCTAAGATCCCTTATAAGGCCATCGCACTTGCCACTGTGCTGTTTTTGATTGGCGCCTT ACCCCTCCTAAGATCCCTTATAAGGCCATCGCGCTTGCCACTGTGCTGTTTTTGATTGGCGCCTT T C TMEM230 Ensembl:ENSG00000089063 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6107576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778597,Human_RBP_ID_4653126 Human_Splice_Rec_2057866,Human_Splice_Rec_2057867,Human_Splice_Rec_2057874,Human_Splice_Rec_2057875,Human_Splice_Rec_2057882,Human_Splice_Rec_2057883,Human_Splice_Rec_2057888,Human_Splice_Rec_2057889,Human_Splice_Rec_2057894,Human_Splice_Rec_2057895,Human_Splice_Rec_2057902,Human_Splice_Rec_2057903,Human_Splice_Rec_2057908,Human_Splice_Rec_2057909,Human_Splice_Rec_2057912,Human_Splice_Rec_2057913,Human_Splice_Rec_2057918,Human_Splice_Rec_2057919,Human_Splice_Rec_2057926,Human_Splice_Rec_2057927,Human_Splice_Rec_2057934 Human_miRNA_ID_1996976,Human_miRNA_ID_2229469,Human_miRNA_ID_2505440 RMVar_hsa_circ_270115,RMVar_hsa_circ_345358,RMVar_hsa_circ_208574 78170 RMVar_ID_78170 Human_SNP_ID_672331440 m1A Human chr20 + 5112839 5112838 5112839 AAACGGGCTTCTGGAAAGAGGCCAACTGTGCCAGGGGGGACGAATGCCCCACACGGATGACTCGG AAACGGGCTTCTGGAAAGAGGCCAACTGTGCC_GGGGGGACGAATGCCCCACACGGATGACTCGG CA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:5112807..5112906 32194978 MeRIP-seq:(Medium) rs568944065 Functional Loss DEL dbSNP153 33..33 33 - - - 78171 RMVar_ID_78171 Human_SNP_ID_672331533 m1A Human chr20 + 5113032 5113032 5113032 CCCACGGTTGGCAGCGCCCAAGGTTGCATGGCATGGCCCGCTTAAGTGCCACTCAGCCGGCCCCA CCCACGGTTGGCAGCGCCCAAGGTTGCATGGCGTGGCCCGCTTAAGTGCCACTCAGCCGGCCCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:5112837..5113045;chr20:5112891..5113075 26863196 MeRIP-seq:(Medium) rs1282666628 Functional Loss SNV dbSNP153 33..33 33 - - - 78172 RMVar_ID_78172 Human_SNP_ID_672331534 m1A Human chr20 - 5113033 5113033 5113033 CTGGGGCCGGCTGAGTGGCACTTAAGCGGGCCATGCCATGCAACCTTGGGCGCTGCCAACCGTGG CTGGGGCCGGCTGAGTGGCACTTAAGCGGGCCGTGCCATGCAACCTTGGGCGCTGCCAACCGTGG T C TMEM230 Ensembl:ENSG00000089063 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr20:5112821..5113047;chr20:5112795..5113050;chr20:5112801..5113075 26863196 MeRIP-seq:(Medium) rs932652748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659656,Human_RBP_ID_7012907,Human_RBP_ID_9118187,Human_RBP_ID_18422813,Human_RBP_ID_22453302,Human_RBP_ID_27022902 Human_Splice_Rec_2057871,Human_Splice_Rec_2057915,Human_Splice_Rec_2057921 RMVar_hsa_circ_76255,RMVar_hsa_circ_208575 78173 RMVar_ID_78173 Human_SNP_ID_672333142 m1A Human chr20 - 5118826 5118826 5118826 AAATACTAAAATGCGCCGGCAATGAAGATATCATTACACTAAGGGCCGAAGATAACGCGGATACC AAATACTAAAATGCGCCGGCAATGAAGATATCGTTACACTAAGGGCCGAAGATAACGCGGATACC T C PCNA Ensembl:ENSG00000132646 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:5118776..5118875 32194978 MeRIP-seq:(Medium) rs1279931603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63101,Human_RBP_ID_925226,Human_RBP_ID_1026730,Human_RBP_ID_1599250,Human_RBP_ID_1931666,Human_RBP_ID_3651488,Human_RBP_ID_4653181,Human_RBP_ID_5503547,Human_RBP_ID_7012983,Human_RBP_ID_8260440,Human_RBP_ID_8856005,Human_RBP_ID_9118202,Human_RBP_ID_9298232,Human_RBP_ID_14142147,Human_RBP_ID_17700770,Human_RBP_ID_17974131,Human_RBP_ID_18516101,Human_RBP_ID_18534845,Human_RBP_ID_18775394,Human_RBP_ID_22506874,Human_RBP_ID_22817820,Human_RBP_ID_24379325,Human_RBP_ID_27298629,Human_RBP_ID_27703113 Human_Splice_Rec_2057936,Human_Splice_Rec_2057937,Human_Splice_Rec_2057948,Human_Splice_Rec_2057949 RMVar_hsa_circ_99802,RMVar_hsa_circ_90925,RMVar_hsa_circ_208578,RMVar_hsa_circ_107242,RMVar_hsa_circ_208579,RMVar_hsa_circ_208580 78174 RMVar_ID_78174 Human_SNP_ID_672333525 m1A Human chr20 - 5119851 5119851 5119851 TCGCTCTGAGGCTCCTGAAGCCGAAACCAGCTAGACTTTCCTCCTTCCCGCCTGCCTGTAGCGGC TCGCTCTGAGGCTCCTGAAGCCGAAACCAGCTGGACTTTCCTCCTTCCCGCCTGCCTGTAGCGGC T C PCNA Ensembl:ENSG00000132646 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:5119826..5119850 26863196 MeRIP-seq:(Medium) rs758579775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1599268,Human_RBP_ID_1931673,Human_RBP_ID_4653204,Human_RBP_ID_5472019,Human_RBP_ID_9331423,Human_RBP_ID_18775403,Human_RBP_ID_22452697,Human_RBP_ID_22817826,Human_RBP_ID_26342337,Human_RBP_ID_27298635,Human_RBP_ID_27564718 Human_Splice_Rec_2057946 Human_miRNA_ID_3078937 RMVar_hsa_circ_99802,RMVar_hsa_circ_208578,RMVar_hsa_circ_107242,RMVar_hsa_circ_208582,RMVar_hsa_circ_124593,RMVar_hsa_circ_208580,RMVar_hsa_circ_114459,RMVar_hsa_circ_208581 78175 RMVar_ID_78175 Human_SNP_ID_672335458 m1A Human chr20 + 5127098 5127098 5127098 CGGCGACGTCGGGCCGATTTTCCCAGGATGACAGAGCTGAGGCAGAGGGTGGCCCATGAGCCGGT CGGCGACGTCGGGCCGATTTTCCCAGGATGACCGAGCTGAGGCAGAGGGTGGCCCATGAGCCGGT A C CDS2 Ensembl:ENSG00000101290 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:5126834..5127218;chr20:5126915..5127185 26863196 MeRIP-seq:(Medium) rs963965935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244785,Human_RBP_ID_3960571,Human_RBP_ID_4653223,Human_RBP_ID_7013005,Human_RBP_ID_14142197,Human_RBP_ID_17658966,Human_RBP_ID_23910704 Human_Splice_Rec_2057957,Human_Splice_Rec_2057967,Human_Splice_Rec_2057983,Human_Splice_Rec_2058007,Human_Splice_Rec_2058027 78176 RMVar_ID_78176 Human_SNP_ID_672335459 m1A Human chr20 + 5127098 5127098 5127098 CGGCGACGTCGGGCCGATTTTCCCAGGATGACAGAGCTGAGGCAGAGGGTGGCCCATGAGCCGGT CGGCGACGTCGGGCCGATTTTCCCAGGATGACGGAGCTGAGGCAGAGGGTGGCCCATGAGCCGGT A G CDS2 Ensembl:ENSG00000101290 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:5126834..5127218;chr20:5126915..5127185 26863196 MeRIP-seq:(Medium) rs963965935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244785,Human_RBP_ID_3960571,Human_RBP_ID_4653223,Human_RBP_ID_7013005,Human_RBP_ID_14142197,Human_RBP_ID_17658966,Human_RBP_ID_23910704 Human_Splice_Rec_2057957,Human_Splice_Rec_2057967,Human_Splice_Rec_2057983,Human_Splice_Rec_2058007,Human_Splice_Rec_2058027 78177 RMVar_ID_78177 Human_SNP_ID_672342861 m1A Human chr20 + 5156312 5156312 5156312 ACAGTGTTTTCCATGGGGCACATTTCAGGGAGATTAGGGTCTTGAAGGAAAGCAGAAGGATGAAC ACAGTGTTTTCCATGGGGCACATTTCAGGGAGGTTAGGGTCTTGAAGGAAAGCAGAAGGATGAAC A G CDS2 Ensembl:ENSG00000101290 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:5156306..5156437 26863196 MeRIP-seq:(Medium) rs1203965484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7013109,Human_RBP_ID_14142741 78178 RMVar_ID_78178 Human_SNP_ID_672342871 m1A Human chr20 - 5156372 5156372 5156372 AACAAGATACCTCCAACTCAGTGGGTTCAAAAACAACCACCATCTTTCCCACCCACACTAGTTCA AACAAGATACCTCCAACTCAGTGGGTTCAAAAGCAACCACCATCTTTCCCACCCACACTAGTTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:5156370..5156456 26863196 MeRIP-seq:(Medium) rs1024406922 Functional Loss SNV dbSNP153 33..33 33 - - - 78179 RMVar_ID_78179 Human_SNP_ID_672346899 m1A Human chr20 - 5173471 5173471 5173471 AAGAGAAAAAGGTCAAAAGTGCCGAGTAGACCATTGAGAAGTCTATGCCTGTCATGAGAGATCTG AAGAGAAAAAGGTCAAAAGTGCCGAGTAGACCCTTGAGAAGTCTATGCCTGTCATGAGAGATCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:5173469..5173554 26863196 MeRIP-seq:(Medium) rs1483766405 Functional Loss SNV dbSNP153 33..33 33 - - - 78180 RMVar_ID_78180 Human_SNP_ID_672352749 m1A Human chr20 - 5196918 5196918 5196918 GCTGCTGCCCCTAGGAGTCCTCCAGCTGGATAACAATAAACCAAACCGCTGTCTCCTAATCCCTG GCTGCTGCCCCTAGGAGTCCTCCAGCTGGATAGCAATAAACCAAACCGCTGTCTCCTAATCCCTG T C lnc-PCNA-1 RNACentral:URS00008BFF2C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:5196867..5196940 26863196 MeRIP-seq:(Medium) rs541516916 Functional Loss SNV dbSNP153 33..33 33 - - - 78181 RMVar_ID_78181 Human_SNP_ID_672354208 m1A Human chr20 + 5202408 5202408 5202408 CCATTTTAAATAGGGTGAACAGGGAAGGCCTCACTGCAGAGGTGGTGTTTGGGCAAATGGACACA CCATTTTAAATAGGGTGAACAGGGAAGGCCTCGCTGCAGAGGTGGTGTTTGGGCAAATGGACACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:5202358..5202446 26863196 MeRIP-seq:(Medium) rs1477273921 Functional Loss SNV dbSNP153 33..33 33 - - - 78182 RMVar_ID_78182 Human_SNP_ID_672355401 m1A Human chr20 + 5206480 5206478 5206480 CCTTTTTTTTTTTTGAGACGGAGTTTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCACTACCTT CCTTTTTTTTTTTTGAGACGGAGTTTCACTC__TCGCCCAGGCTGGAGTGCAGTGGCACTACCTT CTA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:5206471..5206599 26863196 MeRIP-seq:(Medium) rs1368370253 Functional Loss DEL dbSNP153 32..33 33 - - - 78183 RMVar_ID_78183 Human_SNP_ID_672355402 m1A Human chr20 + 5206480 5206480 5206480 CCTTTTTTTTTTTTGAGACGGAGTTTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCACTACCTT CCTTTTTTTTTTTTGAGACGGAGTTTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACTACCTT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:5206471..5206599 26863196 MeRIP-seq:(Medium) rs1296775483 Functional Loss SNV dbSNP153 33..33 33 - - - 78184 RMVar_ID_78184 Human_SNP_ID_672358911 m1A Human chr20 + 5220292 5220292 5220292 TCCTGCCCATTAACACTTCCTATCATCCCTCTATTGCTCACTCCACTACCCCTTCCCAGTGTTTC TCCTGCCCATTAACACTTCCTATCATCCCTCTGTTGCTCACTCCACTACCCCTTCCCAGTGTTTC A G lnc-CDS2-3,lnc-CDS2-3:2 RNACentral:URS00008B9C7C,RNACentral:URS00009C3FAA lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:5220279..5220406 26863196 MeRIP-seq:(Medium) rs1359092244 Functional Loss SNV dbSNP153 33..33 33 - - - 78185 RMVar_ID_78185 Human_SNP_ID_672543287 m1A Human chr20 - 5942524 5942524 5942524 CAAGAGAATGAAGACAGCATGGCAGAGGCCCCAGAGAGCAACCACCCAGAAGACCAGGAAACAAT CAAGAGAATGAAGACAGCATGGCAGAGGCCCCGGAGAGCAACCACCCAGAAGACCAGGAAACAAT T C TRMT6 Ensembl:ENSG00000089195 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:5942479..5942582 26863196 MeRIP-seq:(Medium) rs1057278024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14157628 Human_Splice_Rec_2058777,Human_Splice_Rec_2058797,Human_Splice_Rec_2058817,Human_Splice_Rec_2058831 Human_miRNA_ID_2425734,Human_miRNA_ID_2435403 RMVar_hsa_circ_117131,RMVar_hsa_circ_324545,RMVar_hsa_circ_208621 78186 RMVar_ID_78186 Human_SNP_ID_672545319 m1A Human chr20 - 5950376 5950376 5950376 GTCATGGAGGGCTCAGGGGAGCAGCCGGGCCCACAACCACAGCATCCCGGAGACCACCGCATCCG GTCATGGAGGGCTCAGGGGAGCAGCCGGGCCCGCAACCACAGCATCCCGGAGACCACCGCATCCG T C TRMT6 Ensembl:ENSG00000089195 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:5950327..5950512 26863196 MeRIP-seq:(Medium) rs770900606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924330,Human_RBP_ID_4655125,Human_RBP_ID_9388597,Human_RBP_ID_18422816,Human_RBP_ID_27820062 Human_Splice_Rec_2058765,Human_Splice_Rec_2058785,Human_Splice_Rec_2058805,Human_Splice_Rec_2058821,Human_Splice_Rec_2058839 78187 RMVar_ID_78187 Human_SNP_ID_672545352 m1A Human chr20 - 5950437 5950437 5950437 GGCGGTGGCGACAACCGAGGAGGAGGGGCGGGACGCCGTGGAGCACGGCGACCGGCTGAGCGTCA GGCGGTGGCGACAACCGAGGAGGAGGGGCGGGGCGCCGTGGAGCACGGCGACCGGCTGAGCGTCA T C TRMT6 Ensembl:ENSG00000089195 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:5950260..5950525 26863196 MeRIP-seq:(Medium) rs1468440559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4665428,Human_RBP_ID_9388597,Human_RBP_ID_18422816,Human_RBP_ID_27820062 78188 RMVar_ID_78188 Human_SNP_ID_672545506 m1A Human chr20 - 5950763 5950763 5950763 CAACGGCTCGGGAAACTCAGTTTCCCCACCGCAGCTTCCAGAAGGTGTCTGTAGCGCACAGCGCC CAACGGCTCGGGAAACTCAGTTTCCCCACCGCGGCTTCCAGAAGGTGTCTGTAGCGCACAGCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:5950714..5950824 26863196 MeRIP-seq:(Medium) rs1006211020 Functional Loss SNV dbSNP153 33..33 33 - - - 78189 RMVar_ID_78189 Human_SNP_ID_672545578 m1A Human chr20 - 5951039 5951039 5951039 TTCTTCAAATACTACTTTATTTACATCTCCTAAGGCTAAAGTTCTTACTTGCTTGGGACAGAGGT TTCTTCAAATACTACTTTATTTACATCTCCTAGGGCTAAAGTTCTTACTTGCTTGGGACAGAGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:5950992..5951092;chr20:5950989..5951109 26863196 MeRIP-seq:(Medium) rs1233082424 Functional Loss SNV dbSNP153 33..33 33 - - - 78190 RMVar_ID_78190 Human_SNP_ID_672551466 m1A Human chr20 + 5973169 5973169 5973169 GGAGACCCCCACATCCTTGTTGTTGGAGATCCAGGCCTAGGAAAAAGTCAAATGCTACAGGTAGA GGAGACCCCCACATCCTTGTTGTTGGAGATCCGGGCCTAGGAAAAAGTCAAATGCTACAGGTAGA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding CDS,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34464794 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_925241,Human_RBP_ID_3960603,Human_RBP_ID_19005073,Human_RBP_ID_23005102 Human_Splice_Rec_2058905,Human_Splice_Rec_2058941,Human_Splice_Rec_2058977,Human_Splice_Rec_2059013,Human_Splice_Rec_2059049 Human_miRNA_ID_2569698,Human_miRNA_ID_2569699 RMVar_hsa_circ_71789,RMVar_hsa_circ_363330,RMVar_hsa_circ_350363,RMVar_hsa_circ_353818,RMVar_hsa_circ_73413,RMVar_hsa_circ_56897,RMVar_hsa_circ_31157,RMVar_hsa_circ_62199,RMVar_hsa_circ_32953,RMVar_hsa_circ_288694,RMVar_hsa_circ_325387,RMVar_hsa_circ_365048,RMVar_hsa_circ_278847,RMVar_hsa_circ_279503,RMVar_hsa_circ_35848,RMVar_hsa_circ_44416,RMVar_hsa_circ_17065,RMVar_hsa_circ_359139,RMVar_hsa_circ_74076,RMVar_hsa_circ_56229,RMVar_hsa_circ_126471,RMVar_hsa_circ_208627,RMVar_hsa_circ_349487,RMVar_hsa_circ_208628 78191 RMVar_ID_78191 Human_SNP_ID_672559938 m1A Human chr20 - 6006434 6006434 6006434 TCCCCGCGCCCGAACAGTGGTTCCGCTGGCCGATCCCGGGCAGCCGCAAGCCAAGAGCGGCCGGA TCCCCGCGCCCGAACAGTGGTTCCGCTGGCCGCTCCCGGGCAGCCGCAAGCCAAGAGCGGCCGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:6006388..6006516 26863196 MeRIP-seq:(Medium) rs1266599278 Functional Loss SNV dbSNP153 33..33 33 - - - 78192 RMVar_ID_78192 Human_SNP_ID_672561721 m1A Human chr20 + 6013459 6013458 6013460 AGGGGAGATGGGGAAGAAGGGAGGCAGGTCACAGAAGGTGAGAGGGCATGGGAACGGATGAAGGA AGGGGAGATGGGGAAGAAGGGAGGCAGGTCAC__AAGGTGAGAGGGCATGGGAACGGATGAAGGA CAG C AL035461.4,CRLS1 Ensembl:ENSG00000286235,Ensembl:ENSG00000088766 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:6013436..6013698 26863196 MeRIP-seq:(Medium) rs930986354 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_831176,Human_RBP_ID_18950233 RMVar_hsa_circ_313765,RMVar_hsa_circ_208629,RMVar_hsa_circ_19119 78193 RMVar_ID_78193 Human_SNP_ID_672744248 m1A Human chr20 - 6767741 6767725 6767741 GGTGTGGGAAGCGGAGCGACTAGCGCAGCGCGAGCCGGGCGCAGCGCGGCGGGGCGAGGACTCCG GGTGTGGGAAGCGGAGCGACTAGCGCAGCGCG________________GCGGGGCGAGGACTCCG CCGCGCTGCGCCCGGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:6767676..6768818 26863196 MeRIP-seq:(Medium) rs1351324491 Functional Loss DEL dbSNP153 33..48 33 - - - 78194 RMVar_ID_78194 Human_SNP_ID_672744474 m1A Human chr20 - 6768323 6768323 6768323 GCAGCCATCCTGGGCGACGCCGGGTCCAGGGAAGGGCACGGCGGCGATCTCGGTGCCAGGCGAGT GCAGCCATCCTGGGCGACGCCGGGTCCAGGGAGGGGCACGGCGGCGATCTCGGTGCCAGGCGAGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:6768276..6768525 26863196 MeRIP-seq:(Medium) rs1450877009 Functional Loss SNV dbSNP153 33..33 33 - - - 78195 RMVar_ID_78195 Human_SNP_ID_672744573 m1A Human chr20 + 6768626 6768626 6768626 CGCACCCCACTTTGCGCCGGTGCCTTTGCCCCAGCGGAGCCTGCTTCGCCATCTCCGAGCCCCAC CGCACCCCACTTTGCGCCGGTGCCTTTGCCCCGGCGGAGCCTGCTTCGCCATCTCCGAGCCCCAC A G BMP2 Ensembl:ENSG00000125845 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:6768601..6768625 26863196 MeRIP-seq:(Medium) rs1372102813 Functional Loss SNV dbSNP153 33..33 33 - - - 78196 RMVar_ID_78196 Human_SNP_ID_673115217 m1A Human chr20 + 8242688 8242688 8242688 AAAAGAGAGGAATGGCAATTGCTGAGGATGCAAGAAGTTACCTTGAAAGAAGGAAAAGCAGGATT AAAAGAGAGGAATGGCAATTGCTGAGGATGCAGGAAGTTACCTTGAAAGAAGGAAAAGCAGGATT A G PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:8242649..8242732 26863196 MeRIP-seq:(Medium) rs1218885104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360013 78197 RMVar_ID_78197 Human_SNP_ID_673133455 m1A Human chr20 + 8320877 8320877 8320877 GGGAGGGAAAGAGAGAGAAAGAAAAGAAAGAAAAAGGAAAGAAAGAAAGAGAGAAGAAGAAAAGA GGGAGGGAAAGAGAGAGAAAGAAAAGAAAGAAGAAGGAAAGAAAGAAAGAGAGAAGAAGAAAAGA A G PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:8320865..8321012 26863196 MeRIP-seq:(Medium) rs1472077341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925253,Human_RBP_ID_24546716 RMVar_hsa_circ_360013 78198 RMVar_ID_78198 Human_SNP_ID_673309837 m1A Human chr20 + 9068611 9068611 9068611 GCGCCCACTCCTCGCCCTGCGGGCTCGCGGCAACTGGGCGGCCGGCCCGGCCCCTGCCCACCCCC GCGCCCACTCCTCGCCCTGCGGGCTCGCGGCAGCTGGGCGGCCGGCCCGGCCCCTGCCCACCCCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:9068529..9068642 26863196 MeRIP-seq:(Medium) rs867180351 Functional Loss SNV dbSNP153 33..33 33 - - - 78199 RMVar_ID_78199 Human_SNP_ID_673309838 m1A Human chr20 + 9068611 9068611 9068611 GCGCCCACTCCTCGCCCTGCGGGCTCGCGGCAACTGGGCGGCCGGCCCGGCCCCTGCCCACCCCC GCGCCCACTCCTCGCCCTGCGGGCTCGCGGCATCTGGGCGGCCGGCCCGGCCCCTGCCCACCCCC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:9068529..9068642 26863196 MeRIP-seq:(Medium) rs867180351 Functional Loss SNV dbSNP153 33..33 33 - - - 78200 RMVar_ID_78200 Human_SNP_ID_673318729 m1A Human chr20 + 9108035 9108034 9108035 GTGAAGGGGATTCCAAGGTTTTGTGCCTGGGCAATTGAAAAGATGGAAGTGCTATTTGCTAGAAT GTGAAGGGGATTCCAAGGTTTTGTGCCTGGGC_ATTGAAAAGATGGAAGTGCTATTTGCTAGAAT CA C PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9108026..9108109 26863196 MeRIP-seq:(Medium) rs1337617010 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 78201 RMVar_ID_78201 Human_SNP_ID_673326290 m1A Human chr20 + 9142162 9142162 9142162 GTTTTGATGAGGAAGAGGCTGGAGCCAGAGACACCTCCTGGGAGATGTTGTGGTCAGCACCACAA GTTTTGATGAGGAAGAGGCTGGAGCCAGAGACGCCTCCTGGGAGATGTTGTGGTCAGCACCACAA A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:9142161..9142319 26863196 MeRIP-seq:(Medium) rs1042945085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 78202 RMVar_ID_78202 Human_SNP_ID_673334674 m1A Human chr20 + 9179132 9179132 9179132 CACAGATTTTTTGAGGACCACAATTATGGGTAATGGGATATCACTGAAGGATTTTGAATAGGGGA CACAGATTTTTTGAGGACCACAATTATGGGTACTGGGATATCACTGAAGGATTTTGAATAGGGGA A C PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:9179129..9179309 26863196 MeRIP-seq:(Medium) rs1295016555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 78203 RMVar_ID_78203 Human_SNP_ID_673343437 m1A Human chr20 + 9217320 9217320 9217320 AATTTACATTAGATTCTGATTTTGAAGTGCAAAGGACTGTTTTTCTCCATGAAAACTCTAAAAGT AATTTACATTAGATTCTGATTTTGAAGTGCAAGGGACTGTTTTTCTCCATGAAAACTCTAAAAGT A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:9217317..9217408 26863196 MeRIP-seq:(Medium) rs1237760001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 78204 RMVar_ID_78204 Human_SNP_ID_673343440 m1A Human chr20 - 9217333 9217333 9217333 ATCGATGTAAAGGACTTTTAGAGTTTTCATGGAGAAAAACAGTCCTTTGCACTTCAAAATCAGAA ATCGATGTAAAGGACTTTTAGAGTTTTCATGGGGAAAAACAGTCCTTTGCACTTCAAAATCAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:9217330..9217413 26863196 MeRIP-seq:(Medium) rs988689555 Functional Loss SNV dbSNP153 33..33 33 - - - 78205 RMVar_ID_78205 Human_SNP_ID_673347360 m1A Human chr20 + 9235031 9235031 9235031 TTTGGGGAATTAACAAAGCAAGTATTCTGGAAAGAGAATGAGGCAAGGGAGTGAAGAGTGGTTGT TTTGGGGAATTAACAAAGCAAGTATTCTGGAAGGAGAATGAGGCAAGGGAGTGAAGAGTGGTTGT A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9235026..9235177 26863196 MeRIP-seq:(Medium) rs1332474833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208667,RMVar_hsa_circ_327827,RMVar_hsa_circ_340982,RMVar_hsa_circ_346756,RMVar_hsa_circ_39274,RMVar_hsa_circ_108200,RMVar_hsa_circ_208668 78206 RMVar_ID_78206 Human_SNP_ID_673353189 m1A Human chr20 + 9262254 9262253 9262254 AGATCAGAGACATTCACAAGGACTATAATAAGAAAGAGTATGATAGCTCAACATGAGAGAATAGA AGATCAGAGACATTCACAAGGACTATAATAAG_AAGAGTATGATAGCTCAACATGAGAGAATAGA GA G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9262252..9262352 26863196 MeRIP-seq:(Medium) rs1222184214 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_208667,RMVar_hsa_circ_327827,RMVar_hsa_circ_340982,RMVar_hsa_circ_346756,RMVar_hsa_circ_39274,RMVar_hsa_circ_108200,RMVar_hsa_circ_208668 78207 RMVar_ID_78207 Human_SNP_ID_673359737 m1A Human chr20 + 9293077 9293077 9293077 CTCCACCCTGGGTGACAGAGTGAGATTCAAGAAAGAAAGAAAGAAAGAAAAAGAGAGAGAGACAC CTCCACCCTGGGTGACAGAGTGAGATTCAAGAGAGAAAGAAAGAAAGAAAAAGAGAGAGAGACAC A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:9293074..9293591 26863196 MeRIP-seq:(Medium) rs1021972006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208667,RMVar_hsa_circ_327827,RMVar_hsa_circ_340982,RMVar_hsa_circ_346756,RMVar_hsa_circ_39274,RMVar_hsa_circ_108200,RMVar_hsa_circ_208668 78208 RMVar_ID_78208 Human_SNP_ID_673384625 m1A Human chr20 + 9402412 9402412 9402412 TAGAGTGGCTTGAGTGAGGGTGGAGTGAGACGAGATGAGGCAGGTAGGTGGGAACTGGGTGATGT TAGAGTGGCTTGAGTGAGGGTGGAGTGAGACGCGATGAGGCAGGTAGGTGGGAACTGGGTGATGT A C PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9402328..9402513 26863196 MeRIP-seq:(Medium) rs142430817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76629,RMVar_hsa_circ_11565,RMVar_hsa_circ_67635,RMVar_hsa_circ_29188,RMVar_hsa_circ_208672,RMVar_hsa_circ_341046,RMVar_hsa_circ_363214,RMVar_hsa_circ_208675,RMVar_hsa_circ_208676,RMVar_hsa_circ_43177,RMVar_hsa_circ_27258,RMVar_hsa_circ_50629 78209 RMVar_ID_78209 Human_SNP_ID_673384656 m1A Human chr20 + 9402621 9402621 9402621 ACAGGAGTGGAAGCAGGAAAAGCAGTGAGGACAGGCTGCTGCTCTAGGCCAGACGAGAGTCCCCG ACAGGAGTGGAAGCAGGAAAAGCAGTGAGGACTGGCTGCTGCTCTAGGCCAGACGAGAGTCCCCG A T PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9402573..9402697 26863196 MeRIP-seq:(Medium) rs1463115251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76629,RMVar_hsa_circ_11565,RMVar_hsa_circ_67635,RMVar_hsa_circ_29188,RMVar_hsa_circ_208672,RMVar_hsa_circ_341046,RMVar_hsa_circ_363214,RMVar_hsa_circ_208675,RMVar_hsa_circ_208676,RMVar_hsa_circ_43177,RMVar_hsa_circ_27258,RMVar_hsa_circ_50629 78210 RMVar_ID_78210 Human_SNP_ID_673539279 m1A Human chr20 + 10036900 10036900 10036900 AGACACCAGGGGAGTGTGTGAGGACAGAAAAGAGTCTTGAGGACCTAGCCCTGGGCACCCAACAT AGACACCAGGGGAGTGTGTGAGGACAGAAAAGCGTCTTGAGGACCTAGCCCTGGGCACCCAACAT A C ANKEF1 Ensembl:ENSG00000132623 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:10036897..10037060 26863196 MeRIP-seq:(Medium) rs1017424644 Functional Loss SNV dbSNP153 33..33 33 - - - 78211 RMVar_ID_78211 Human_SNP_ID_673539280 m1A Human chr20 + 10036900 10036900 10036900 AGACACCAGGGGAGTGTGTGAGGACAGAAAAGAGTCTTGAGGACCTAGCCCTGGGCACCCAACAT AGACACCAGGGGAGTGTGTGAGGACAGAAAAGGGTCTTGAGGACCTAGCCCTGGGCACCCAACAT A G ANKEF1 Ensembl:ENSG00000132623 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:10036897..10037060 26863196 MeRIP-seq:(Medium) rs1017424644 Functional Loss SNV dbSNP153 33..33 33 - - - 78212 RMVar_ID_78212 Human_SNP_ID_673539310 m1A Human chr20 + 10037028 10037028 10037028 GAAGCAGGCGATGGAGATGTTGTGGTGCCTAGAGAGACACATTTAAAGGAGAGAGAGCTCACTGC GAAGCAGGCGATGGAGATGTTGTGGTGCCTAGGGAGACACATTTAAAGGAGAGAGAGCTCACTGC A G ANKEF1 Ensembl:ENSG00000132623 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:10037025..10037099 26863196 MeRIP-seq:(Medium) rs993941520 Functional Loss SNV dbSNP153 33..33 33 - - - 78213 RMVar_ID_78213 Human_SNP_ID_673585508 m1A Human chr20 + 10218976 10218976 10218976 GGCCCGGAGAACACAACCCTCCCGAGAAGCCCAGGTAAGAACCCCCCTCCCCAGGTCGTGGCTCT GGCCCGGAGAACACAACCCTCCCGAGAAGCCCGGGTAAGAACCCCCCTCCCCAGGTCGTGGCTCT A G SNAP25 Ensembl:ENSG00000132639 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:10218884..10219034 26863196 MeRIP-seq:(Medium) rs895098906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2061181,Human_Splice_Rec_2061195 78214 RMVar_ID_78214 Human_SNP_ID_673598075 m1A Human chr20 - 10275478 10275478 10275478 TGTCTGCGTCTTCGGCCATGGTAGCGGTGGGGAGTGGCTGGGCGCCTGGGCTGGGGGGTCAGTGA TGTCTGCGTCTTCGGCCATGGTAGCGGTGGGGGGTGGCTGGGCGCCTGGGCTGGGGGGTCAGTGA T C SNAP25-AS1 Ensembl:ENSG00000227906 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:10275397..10275480 26863196 MeRIP-seq:(Medium) rs1304464507 Functional Loss SNV dbSNP153 33..33 33 - - - 78215 RMVar_ID_78215 Human_SNP_ID_673598081 m1A Human chr20 + 10275483 10275482 10275483 GACCCCCCAGCCCAGGCGCCCAGCCACTCCCCACCGCTACCATGGCCGAAGACGCAGACATGCGC GACCCCCCAGCCCAGGCGCCCAGCCACTCCCC_CCGCTACCATGGCCGAAGACGCAGACATGCGC CA C SNAP25 Ensembl:ENSG00000132639 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:10275388..10277698;chr20:10275386..10275514 26863196 MeRIP-seq:(Medium) rs1383475175 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9114969 Human_Splice_Rec_2061182,Human_Splice_Rec_2061183,Human_Splice_Rec_2061196,Human_Splice_Rec_2061197,Human_Splice_Rec_2061210,Human_Splice_Rec_2061211,Human_Splice_Rec_2061217 Human_miRNA_ID_2368381,Human_miRNA_ID_2726708,Human_miRNA_ID_3016164 RMVar_hsa_circ_24675,RMVar_hsa_circ_208700,RMVar_hsa_circ_377666,RMVar_hsa_circ_208701,RMVar_hsa_circ_269062,RMVar_hsa_circ_208702,RMVar_hsa_circ_208703 78216 RMVar_ID_78216 Human_SNP_ID_673598082 m1A Human chr20 + 10275483 10275483 10275483 GACCCCCCAGCCCAGGCGCCCAGCCACTCCCCACCGCTACCATGGCCGAAGACGCAGACATGCGC GACCCCCCAGCCCAGGCGCCCAGCCACTCCCCGCCGCTACCATGGCCGAAGACGCAGACATGCGC A G SNAP25 Ensembl:ENSG00000132639 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:10275388..10277698;chr20:10275386..10275514 26863196 MeRIP-seq:(Medium) rs41306792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9114969 Human_Splice_Rec_2061182,Human_Splice_Rec_2061183,Human_Splice_Rec_2061196,Human_Splice_Rec_2061197,Human_Splice_Rec_2061210,Human_Splice_Rec_2061211,Human_Splice_Rec_2061217 Human_miRNA_ID_2368381,Human_miRNA_ID_2726708,Human_miRNA_ID_3016164 RMVar_hsa_circ_24675,RMVar_hsa_circ_208700,RMVar_hsa_circ_377666,RMVar_hsa_circ_208701,RMVar_hsa_circ_269062,RMVar_hsa_circ_208702,RMVar_hsa_circ_208703 78217 RMVar_ID_78217 Human_SNP_ID_673635213 m1A Human chr20 - 10434015 10434015 10434015 AGGGGCTTGTAGGCGCCTCCCTCTCCACCCCCAAAGGTCACCGGTGTCCTCACTGAAGGATATTT AGGGGCTTGTAGGCGCCTCCCTCTCCACCCCCTAAGGTCACCGGTGTCCTCACTGAAGGATATTT T A MKKS Ensembl:ENSG00000125863 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:10433996..10434124 26863196 MeRIP-seq:(Medium) rs1204542947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5383328,Human_RBP_ID_19105940 78218 RMVar_ID_78218 Human_SNP_ID_673692090 m1A Human chr20 + 10673771 10673771 10673771 CCTCCTTTTATTATTCTGATCGCTTCTTTGAGACGCTCCCCCTCCTCTTCCACCTCCCGGCTTTC CCTCCTTTTATTATTCTGATCGCTTCTTTGAGGCGCTCCCCCTCCTCTTCCACCTCCCGGCTTTC A G AL050403.2 Ensembl:ENSG00000270792 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:10673721..10673943 26863196 MeRIP-seq:(Medium) rs377227562 Functional Loss SNV dbSNP153 33..33 33 - - - 78219 RMVar_ID_78219 Human_SNP_ID_673997386 m1A Human chr20 + 11891304 11891304 11891304 GGAGGGGCGCACGAGCCCGCCTGGCCGTGCGGACGCCCGCGGGGTGCGCGACCCCGGAGGTGGCG GGAGGGGCGCACGAGCCCGCCTGGCCGTGCGGTCGCCCGCGGGGTGCGCGACCCCGGAGGTGGCG A T BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:11891276..11891499 26863196 MeRIP-seq:(Medium) rs1317531284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244520,Human_RBP_ID_1068242,Human_RBP_ID_5383352 RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 78220 RMVar_ID_78220 Human_SNP_ID_673997463 m1A Human chr20 + 11891513 11891513 11891513 CGGGGACCGACGCTCCGGGTTTGCGCGGCCTCAGGCGCCGCGGGAACCCAGCGAGTGGCGGCGGG CGGGGACCGACGCTCCGGGTTTGCGCGGCCTCGGGCGCCGCGGGAACCCAGCGAGTGGCGGCGGG A G BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:11891502..11891636 32194978 MeRIP-seq:(Medium) rs933428795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18462871 RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 78221 RMVar_ID_78221 Human_SNP_ID_674006089 m1A Human chr20 + 11925892 11925892 11925892 GCTGCTGGTGAAAGTCGTGTGAAATCCTGTACACTGTGTATAGAATAATGTAATTTTATGTTAAT GCTGCTGGTGAAAGTCGTGTGAAATCCTGTACGCTGTGTATAGAATAATGTAATTTTATGTTAAT A G BTBD3 Ensembl:ENSG00000132640 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:11925841..11925919 32194978 MeRIP-seq:(Medium) rs1196701812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1593119,Human_RBP_ID_1926009,Human_RBP_ID_9115136,Human_RBP_ID_18768528 RMVar_hsa_circ_109284,RMVar_hsa_circ_208733,RMVar_hsa_circ_208735,RMVar_hsa_circ_208736 78222 RMVar_ID_78222 Human_SNP_ID_674351860 m1A Human chr20 + 13270569 13270569 13270569 GAAACCAGCTTTTCTCTCTCCAAAGAAGCACCAAGGGAGCATCTGGACCACCAGGCTGCACACCA GAAACCAGCTTTTCTCTCTCCAAAGAAGCACCGAGGGAGCATCTGGACCACCAGGCTGCACACCA A G ISM1 Ensembl:ENSG00000101230 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:13270534..13270660 26863196 MeRIP-seq:(Medium) rs750786293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2062076 RMVar_hsa_circ_208746,RMVar_hsa_circ_314504,RMVar_hsa_circ_330978,RMVar_hsa_circ_353010,RMVar_hsa_circ_303753,RMVar_hsa_circ_208745 78223 RMVar_ID_78223 Human_SNP_ID_674466504 m1A Human chr20 - 13759810 13759810 13759810 GTCAATGTAGAAGAAGATGGGAAAACAAAGAAAAGTCAGAAGGATGATGAAGAACAAATTGCTAA GTCAATGTAGAAGAAGATGGGAAAACAAAGAAGAGTCAGAAGGATGATGAAGAACAAATTGCTAA T C ESF1 Ensembl:ENSG00000089048 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:13759697..13766868 26863196 MeRIP-seq:(Medium) rs375092735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62153,Human_RBP_ID_925299,Human_RBP_ID_1926137,Human_RBP_ID_2677297,Human_RBP_ID_24546719 Human_Splice_Rec_2062222,Human_Splice_Rec_2062246 RMVar_hsa_circ_47137,RMVar_hsa_circ_361273,RMVar_hsa_circ_330764,RMVar_hsa_circ_304298,RMVar_hsa_circ_70483,RMVar_hsa_circ_310619,RMVar_hsa_circ_72487,RMVar_hsa_circ_361797,RMVar_hsa_circ_278899,RMVar_hsa_circ_358209,RMVar_hsa_circ_65573 78224 RMVar_ID_78224 Human_SNP_ID_674468284 m1A Human chr20 + 13766865 13766865 13766865 TGAAAATCCATGTCCAAAAGCTCTTCCTTTTTAAACTTCCTGTTGAGCATTGTAATTCTTTCATG TGAAAATCCATGTCCAAAAGCTCTTCCTTTTTCAACTTCCTGTTGAGCATTGTAATTCTTTCATG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:13766740..13766872 26863196 MeRIP-seq:(Medium) rs777045761 Functional Loss SNV dbSNP153 33..33 33 - - - 78225 RMVar_ID_78225 Human_SNP_ID_674470617 m1A Human chr20 - 13776062 13776044 13776062 AGTGAAGATGATGAAGAGGAGGATGAAGATGAAGAGGAGGATGAAGATGAGGATAGTGAGGATGA AGTGAAGATGATGAAGAGGAGGATGAAGATGA__________________GGATAGTGAGGATGA CTCATCTTCATCCTCCTCT C ESF1 Ensembl:ENSG00000089048 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13775975..13776225 26863196 MeRIP-seq:(Medium) rs751194986 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_62160,Human_RBP_ID_206546,Human_RBP_ID_1601113,Human_RBP_ID_2677318,Human_RBP_ID_5148298,Human_RBP_ID_6979952,Human_RBP_ID_8260218,Human_RBP_ID_18534380,Human_RBP_ID_21983996,Human_RBP_ID_22081554,Human_RBP_ID_23004742,Human_RBP_ID_23115397,Human_RBP_ID_23119586,Human_RBP_ID_23894563,Human_RBP_ID_24546638,Human_RBP_ID_26342696 RMVar_hsa_circ_361273,RMVar_hsa_circ_358209,RMVar_hsa_circ_75021,RMVar_hsa_circ_319772,RMVar_hsa_circ_61776 78226 RMVar_ID_78226 Human_SNP_ID_674470624 m1A Human chr20 - 13776062 13776058 13776063 AGTGAAGATGATGAAGAGGAGGATGAAGATGAAGAGGAGGATGAAGATGAGGATAGTGAGGATGA AGTGAAGATGATGAAGAGGAGGATGAAGATG_____GAGGATGAAGATGAGGATAGTGAGGATGA CCTCTT C ESF1 Ensembl:ENSG00000089048 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13775975..13776225 26863196 MeRIP-seq:(Medium) rs767761561 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_62160,Human_RBP_ID_206546,Human_RBP_ID_1601113,Human_RBP_ID_2677318,Human_RBP_ID_5148298,Human_RBP_ID_6979952,Human_RBP_ID_8260218,Human_RBP_ID_18534380,Human_RBP_ID_21983996,Human_RBP_ID_22081554,Human_RBP_ID_23004742,Human_RBP_ID_23115397,Human_RBP_ID_23119586,Human_RBP_ID_23894563,Human_RBP_ID_24546638,Human_RBP_ID_26342696 RMVar_hsa_circ_361273,RMVar_hsa_circ_358209,RMVar_hsa_circ_75021,RMVar_hsa_circ_319772,RMVar_hsa_circ_61776 78227 RMVar_ID_78227 Human_SNP_ID_674470627 m1A Human chr20 - 13776062 13776059 13776062 AGTGAAGATGATGAAGAGGAGGATGAAGATGAAGAGGAGGATGAAGATGAGGATAGTGAGGATGA AGTGAAGATGATGAAGAGGAGGATGAAGATGA___GGAGGATGAAGATGAGGATAGTGAGGATGA CTCT C ESF1 Ensembl:ENSG00000089048 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13775975..13776225 26863196 MeRIP-seq:(Medium) rs764551794 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_62160,Human_RBP_ID_206546,Human_RBP_ID_1601113,Human_RBP_ID_2677318,Human_RBP_ID_5148298,Human_RBP_ID_6979952,Human_RBP_ID_8260218,Human_RBP_ID_18534380,Human_RBP_ID_21983996,Human_RBP_ID_22081554,Human_RBP_ID_23004742,Human_RBP_ID_23115397,Human_RBP_ID_23119586,Human_RBP_ID_23894563,Human_RBP_ID_24546638,Human_RBP_ID_26342696 RMVar_hsa_circ_361273,RMVar_hsa_circ_358209,RMVar_hsa_circ_75021,RMVar_hsa_circ_319772,RMVar_hsa_circ_61776 78228 RMVar_ID_78228 Human_SNP_ID_674479607 m1A Human chr20 - 13810962 13810962 13810962 GTCAGTTCACCTTCTCATTCCCTATAATGACTATTTCAAACGGTTCCATTCACTTCTCAAAACTC GTCAGTTCACCTTCTCATTCCCTATAATGACTTTTTCAAACGGTTCCATTCACTTCTCAAAACTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:13810927..13811045 26863196 MeRIP-seq:(Medium) rs1292857117 Functional Loss SNV dbSNP153 33..33 33 - - - 78229 RMVar_ID_78229 Human_SNP_ID_675100529 m1A Human chr20 - 16380130 16380130 16380130 AAACTCATAGAAGAAATGGAGGAAAAGCAGAAATCAGACAAGGCTGAACTGGAGCGGATGCAGCA AAACTCATAGAAGAAATGGAGGAAAAGCAGAACTCAGACAAGGCTGAACTGGAGCGGATGCAGCA T G KIF16B Ensembl:ENSG00000089177 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:16380006..16380135 26863196 MeRIP-seq:(Medium) rs746257532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2062920,Human_Splice_Rec_2062968,Human_Splice_Rec_2063026,Human_Splice_Rec_2063040 RMVar_hsa_circ_67484,RMVar_hsa_circ_11314,RMVar_hsa_circ_71423,RMVar_hsa_circ_61412,RMVar_hsa_circ_208815,RMVar_hsa_circ_350099,RMVar_hsa_circ_66656,RMVar_hsa_circ_7219,RMVar_hsa_circ_67329,RMVar_hsa_circ_208819,RMVar_hsa_circ_208820,RMVar_hsa_circ_208821,RMVar_hsa_circ_286639,RMVar_hsa_circ_287134,RMVar_hsa_circ_265853,RMVar_hsa_circ_208824,RMVar_hsa_circ_208825,RMVar_hsa_circ_208823,RMVar_hsa_circ_312901,RMVar_hsa_circ_208826,RMVar_hsa_circ_127247,RMVar_hsa_circ_8195,RMVar_hsa_circ_208828,RMVar_hsa_circ_208827,RMVar_hsa_circ_90470,RMVar_hsa_circ_319787,RMVar_hsa_circ_208831,RMVar_hsa_circ_63206,RMVar_hsa_circ_208832,RMVar_hsa_circ_208830 78230 RMVar_ID_78230 Human_SNP_ID_675135482 m1A Human chr20 - 16526203 16526203 16526203 ATCATTATTATTCTAATCATTTCTTTCTAGATACCAGAAGGAGGCACTGGGGACTCAGGAAGAGA ATCATTATTATTCTAATCATTTCTTTCTAGATGCCAGAAGGAGGCACTGGGGACTCAGGAAGAGA T C KIF16B Ensembl:ENSG00000089177 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:16526192..16526277 26863196 MeRIP-seq:(Medium) rs1217573788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924352 RMVar_hsa_circ_28623,RMVar_hsa_circ_309432,RMVar_hsa_circ_30021,RMVar_hsa_circ_208840,RMVar_hsa_circ_208843,RMVar_hsa_circ_275719 78231 RMVar_ID_78231 Human_SNP_ID_675146813 m1A Human chr20 - 16573279 16573279 16573279 TAGTGGGACCCCGCGCGGGCTGGTTCGGGATGAGCGATGGCATCGGTCAAGGTGGCCGTGAGGGT TAGTGGGACCCCGCGCGGGCTGGTTCGGGATGGGCGATGGCATCGGTCAAGGTGGCCGTGAGGGT T C KIF16B Ensembl:ENSG00000089177 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:16573195..16573409 26863196 MeRIP-seq:(Medium) rs770182434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8857469,Human_RBP_ID_18422828,Human_RBP_ID_23004935,Human_RBP_ID_23119647,Human_RBP_ID_26342702 Human_Splice_Rec_2062887,Human_Splice_Rec_2062935,Human_Splice_Rec_2062993 78232 RMVar_ID_78232 Human_SNP_ID_675146833 m1A Human chr20 - 16573321 16573321 16573321 ATCTGAGTAGCCAGCGTCGCCGGCGACCGCGGAGTTCTGGGCTAGTGGGACCCCGCGCGGGCTGG ATCTGAGTAGCCAGCGTCGCCGGCGACCGCGGCGTTCTGGGCTAGTGGGACCCCGCGCGGGCTGG T G KIF16B Ensembl:ENSG00000089177 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:16573275..16573409 26863196 MeRIP-seq:(Medium) rs760714203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8857469,Human_RBP_ID_18422828,Human_RBP_ID_23119647 Human_Splice_Rec_2062887,Human_Splice_Rec_2062935,Human_Splice_Rec_2062993 78233 RMVar_ID_78233 Human_SNP_ID_675186973 m1A Human chr20 + 16730084 16730084 16730084 GCGTAGGCCTTAGGTGGGTTCGTGCGCCTTCTACCTCGCTGTTTCGGTTTTCCTGGCTCCTCGGC GCGTAGGCCTTAGGTGGGTTCGTGCGCCTTCTGCCTCGCTGTTTCGGTTTTCCTGGCTCCTCGGC A G SNRPB2 Ensembl:ENSG00000125870 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:16730052..16730217 26863196 MeRIP-seq:(Medium) rs969391213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4636470,Human_RBP_ID_5423535,Human_RBP_ID_9331436,Human_RBP_ID_19107594 Human_Splice_Rec_2063065,Human_Splice_Rec_2063077 78234 RMVar_ID_78234 Human_SNP_ID_675383037 m1A Human chr20 - 17494323 17494323 17494323 TGTGCCATGGTCACACCCGGTGCAGAGGAACCATCTATACCTGAGCCTCCAAAGCCTGCGGCTGA TGTGCCATGGTCACACCCGGTGCAGAGGAACCTTCTATACCTGAGCCTCCAAAGCCTGCGGCTGA T A BFSP1 Ensembl:ENSG00000125864 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6080718 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9329,GWAS_ID_9330,GWAS_ID_9331,GWAS_ID_9332 78235 RMVar_ID_78235 Human_SNP_ID_675383038 m1A Human chr20 - 17494323 17494323 17494323 TGTGCCATGGTCACACCCGGTGCAGAGGAACCATCTATACCTGAGCCTCCAAAGCCTGCGGCTGA TGTGCCATGGTCACACCCGGTGCAGAGGAACCGTCTATACCTGAGCCTCCAAAGCCTGCGGCTGA T C BFSP1 Ensembl:ENSG00000125864 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6080718 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_9329,GWAS_ID_9330,GWAS_ID_9331,GWAS_ID_9332 78236 RMVar_ID_78236 Human_SNP_ID_675401531 m1A Human chr20 - 17569653 17569652 17569653 TGGAGGGGAAAAGGAGGGGAGAGCCGGGGGAGAGGGGTACAGAGTGTGGGAAGGAGGGGGATTTG TGGAGGGGAAAAGGAGGGGAGAGCCGGGGGAG_GGGGTACAGAGTGTGGGAAGGAGGGGGATTTG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17569609..17569709 26863196 MeRIP-seq:(Medium) rs1378339217 Functional Loss DEL dbSNP153 33..33 33 - - - 78237 RMVar_ID_78237 Human_SNP_ID_675401533 m1A Human chr20 - 17569653 17569653 17569653 TGGAGGGGAAAAGGAGGGGAGAGCCGGGGGAGAGGGGTACAGAGTGTGGGAAGGAGGGGGATTTG TGGAGGGGAAAAGGAGGGGAGAGCCGGGGGAGGGGGGTACAGAGTGTGGGAAGGAGGGGGATTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17569609..17569709 26863196 MeRIP-seq:(Medium) rs1201062956 Functional Loss SNV dbSNP153 33..33 33 - - - 78238 RMVar_ID_78238 Human_SNP_ID_675401549 m1A Human chr20 + 17569703 17569703 17569703 TCCTTTTCCCCTCCACGGCCTCGCCCCGCCCCAGCGGCAGGCACACCTGGCCAGGTGGCTGCCTC TCCTTTTCCCCTCCACGGCCTCGCCCCGCCCCCGCGGCAGGCACACCTGGCCAGGTGGCTGCCTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17569656..17569760 26863196 MeRIP-seq:(Medium) rs1413887845 Functional Loss SNV dbSNP153 33..33 33 - - - 78239 RMVar_ID_78239 Human_SNP_ID_675401762 m1A Human chr20 - 17570151 17570151 17570151 CGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCAGACCGTCCTCCTCACGGCTGCGGGACCGAGAG CGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCTGACCGTCCTCCTCACGGCTGCGGGACCGAGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17569861..17570305;chr20:17570026..17570311;chr20:17570076..17570272 26863196 MeRIP-seq:(Medium) rs1394139156 Functional Loss SNV dbSNP153 33..33 33 - - - 78240 RMVar_ID_78240 Human_SNP_ID_675401763 m1A Human chr20 - 17570151 17570151 17570151 CGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCAGACCGTCCTCCTCACGGCTGCGGGACCGAGAG CGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCCGACCGTCCTCCTCACGGCTGCGGGACCGAGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17569861..17570305;chr20:17570026..17570311;chr20:17570076..17570272 26863196 MeRIP-seq:(Medium) rs1394139156 Functional Loss SNV dbSNP153 33..33 33 - - - 78241 RMVar_ID_78241 Human_SNP_ID_675401774 m1A Human chr20 - 17570173 17570171 17570173 CGCCGCGGCGGTCGCAGGGACGCGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCAGACCGTCCTC CGCCGCGGCGGTCGCAGGGACGCGGGGGAGGG__CCGGCGGGCAGCGAGTATGCAGACCGTCCTC GCT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:17570076..17570273 26863196 MeRIP-seq:(Medium) rs961633302 Functional Loss DEL dbSNP153 33..34 33 - - - 78242 RMVar_ID_78242 Human_SNP_ID_675409110 m1A Human chr20 - 17600729 17600725 17600730 ATCAGCTACTTGCACTCCTGAGGCCTATGATGAGAAAATACATGAGAAAAAGACTTACAATTTTT ATCAGCTACTTGCACTCCTGAGGCCTATGAT_____AATACATGAGAAAAAGACTTACAATTTTT TTTCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17600726..17600775 26863196 MeRIP-seq:(Medium) rs774619965 Functional Loss DEL dbSNP153 32..36 33 - - - 78243 RMVar_ID_78243 Human_SNP_ID_675409112 m1A Human chr20 - 17600729 17600728 17600729 ATCAGCTACTTGCACTCCTGAGGCCTATGATGAGAAAATACATGAGAAAAAGACTTACAATTTTT ATCAGCTACTTGCACTCCTGAGGCCTATGATG_GAAAATACATGAGAAAAAGACTTACAATTTTT CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17600726..17600775 26863196 MeRIP-seq:(Medium) rs1456930435 Functional Loss DEL dbSNP153 33..33 33 - - - 78244 RMVar_ID_78244 Human_SNP_ID_675409114 m1A Human chr20 + 17600734 17600734 17600734 TTGTAAGTCTTTTTCTCATGTATTTTCTCATCATAGGCCTCAGGAGTGCAAGTAGCTGATGAAGT TTGTAAGTCTTTTTCTCATGTATTTTCTCATCGTAGGCCTCAGGAGTGCAAGTAGCTGATGAAGT A G DSTN Ensembl:ENSG00000125868 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:17600726..17600775 26863196 MeRIP-seq:(Medium) rs368746357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2709290 RMVar_hsa_circ_22186,RMVar_hsa_circ_208856,RMVar_hsa_circ_110376 78245 RMVar_ID_78245 Human_SNP_ID_675413180 m1A Human chr20 + 17614759 17614756 17614759 AGGCACGCACTGCCTTTTCCAGCTGTTCCTGCAGCTTCTTCACCGTGTCCTTCTCCCTTGCCAGC AGGCACGCACTGCCTTTTCCAGCTGTTCCT___GCTTCTTCACCGTGTCCTTCTCCCTTGCCAGC TGCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17613741..17614917 26863196 MeRIP-seq:(Medium) rs1158885530 Functional Loss DEL dbSNP153 31..33 33 - - - 78246 RMVar_ID_78246 Human_SNP_ID_675413189 m1A Human chr20 - 17614784 17614784 17614784 AGCTTCTGAAGACGACCCAGGAGCAGCTGGCAAGGGAGAAGGACACGGTGAAGAAGCTGCAGGAA AGCTTCTGAAGACGACCCAGGAGCAGCTGGCAGGGGAGAAGGACACGGTGAAGAAGCTGCAGGAA T C RRBP1 Ensembl:ENSG00000125844 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:17614751..17614800 26863196 MeRIP-seq:(Medium) rs758533469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62781,Human_RBP_ID_9388683,Human_RBP_ID_19005123,Human_RBP_ID_24546832,Human_RBP_ID_26342348 Human_Splice_Rec_2063273,Human_Splice_Rec_2063335,Human_Splice_Rec_2063377,Human_Splice_Rec_2063425,Human_Splice_Rec_2063471,Human_Splice_Rec_2063517,Human_Splice_Rec_2063561 RMVar_hsa_circ_59520,RMVar_hsa_circ_109172,RMVar_hsa_circ_208857 78247 RMVar_ID_78247 Human_SNP_ID_675413190 m1A Human chr20 - 17614784 17614784 17614784 AGCTTCTGAAGACGACCCAGGAGCAGCTGGCAAGGGAGAAGGACACGGTGAAGAAGCTGCAGGAA AGCTTCTGAAGACGACCCAGGAGCAGCTGGCACGGGAGAAGGACACGGTGAAGAAGCTGCAGGAA T G RRBP1 Ensembl:ENSG00000125844 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:17614751..17614800 26863196 MeRIP-seq:(Medium) rs758533469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62781,Human_RBP_ID_9388683,Human_RBP_ID_19005123,Human_RBP_ID_24546832,Human_RBP_ID_26342348 Human_Splice_Rec_2063273,Human_Splice_Rec_2063335,Human_Splice_Rec_2063377,Human_Splice_Rec_2063425,Human_Splice_Rec_2063471,Human_Splice_Rec_2063517,Human_Splice_Rec_2063561 RMVar_hsa_circ_59520,RMVar_hsa_circ_109172,RMVar_hsa_circ_208857 78248 RMVar_ID_78248 Human_SNP_ID_675413641 m1A Human chr20 + 17615975 17615975 17615975 TGAGCTTCTGCCGCTGTGTCTGCTCATCCTCCAGGATGGCTTCTGTCCACTCCAGCTGCGTCTTC TGAGCTTCTGCCGCTGTGTCTGCTCATCCTCCGGGATGGCTTCTGTCCACTCCAGCTGCGTCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17615893..17616001 26863196 MeRIP-seq:(Medium) rs965352093 Functional Loss SNV dbSNP153 33..33 33 - - - 78249 RMVar_ID_78249 Human_SNP_ID_675415109 m1A Human chr20 + 17620348 17620348 17620348 GTTCTCCTTTTAGCTTCTCTACAATCTCTTCGAGATGCTTCACTGTGACCCGGGACTACAAAGCA GTTCTCCTTTTAGCTTCTCTACAATCTCTTCGGGATGCTTCACTGTGACCCGGGACTACAAAGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:17620276..17620375 32194978 MeRIP-seq:(Medium) rs374556178 Functional Loss SNV dbSNP153 33..33 33 - - - 78250 RMVar_ID_78250 Human_SNP_ID_675415325 m1A Human chr20 - 17620764 17620762 17620765 CAGAGACCTGCAGAAGAGCGTGGAGGAGGAGGAGCAGGTGTGGAGGGCCAAGGTGGGCGCCGCAG CAGAGACCTGCAGAAGAGCGTGGAGGAGGAG___CAGGTGTGGAGGGCCAAGGTGGGCGCCGCAG GCTC G RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17620656..17620851 26863196 MeRIP-seq:(Medium) rs765361650 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_925314,Human_RBP_ID_8857471,Human_RBP_ID_9388702,Human_RBP_ID_17976683,Human_RBP_ID_18471050,Human_RBP_ID_19005127,Human_RBP_ID_22452908,Human_RBP_ID_26343398 Human_Splice_Rec_2063282,Human_Splice_Rec_2063283,Human_Splice_Rec_2063322,Human_Splice_Rec_2063323,Human_Splice_Rec_2063364,Human_Splice_Rec_2063365,Human_Splice_Rec_2063412,Human_Splice_Rec_2063413,Human_Splice_Rec_2063458,Human_Splice_Rec_2063459,Human_Splice_Rec_2063504,Human_Splice_Rec_2063505,Human_Splice_Rec_2063548,Human_Splice_Rec_2063549 RMVar_hsa_circ_59520,RMVar_hsa_circ_62648 78251 RMVar_ID_78251 Human_SNP_ID_675416582 m1A Human chr20 + 17624650 17624650 17624650 CTCGGCCGTGGCCAGTGCCTCCATGGCCTTCCAGTTCTTCTCCCGGAGGTCCTGGAGGGGACACA CTCGGCCGTGGCCAGTGCCTCCATGGCCTTCCGGTTCTTCTCCCGGAGGTCCTGGAGGGGACACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:17624534..17624675 26863196 MeRIP-seq:(Medium) rs1442025440 Functional Loss SNV dbSNP153 33..33 33 - - - 78252 RMVar_ID_78252 Human_SNP_ID_675416584 m1A Human chr20 - 17624652 17624652 17624652 CCTGTGTCCCCTCCAGGACCTCCGGGAGAAGAACTGGAAGGCCATGGAGGCACTGGCCACGGCCG CCTGTGTCCCCTCCAGGACCTCCGGGAGAAGAGCTGGAAGGCCATGGAGGCACTGGCCACGGCCG T C RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17624601..17627625;chr20:17624601..17627575 26863196 MeRIP-seq:(Medium) rs970036715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924795,Human_RBP_ID_9388715,Human_RBP_ID_18443997,Human_RBP_ID_19005133,Human_RBP_ID_22452914,Human_RBP_ID_22548957,Human_RBP_ID_27819576 Human_Splice_Rec_2063314,Human_Splice_Rec_2063315,Human_Splice_Rec_2063356,Human_Splice_Rec_2063357,Human_Splice_Rec_2063404,Human_Splice_Rec_2063405,Human_Splice_Rec_2063450,Human_Splice_Rec_2063451,Human_Splice_Rec_2063496,Human_Splice_Rec_2063497,Human_Splice_Rec_2063540,Human_Splice_Rec_2063541 Human_miRNA_ID_2804438 RMVar_hsa_circ_33235,RMVar_hsa_circ_59520,RMVar_hsa_circ_91274,RMVar_hsa_circ_208860,RMVar_hsa_circ_208859 78253 RMVar_ID_78253 Human_SNP_ID_675417450 m1A Human chr20 + 17627328 17627328 17627328 GGTCCCCCGGGCTGAGGCTCAAGTGAGCAGGCAGGCTGCTTCCCCAGCTTACCGAGTCTGCTGCT GGTCCCCCGGGCTGAGGCTCAAGTGAGCAGGCGGGCTGCTTCCCCAGCTTACCGAGTCTGCTGCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:17627326..17627400 26863196 MeRIP-seq:(Medium) rs1268323630 Functional Loss SNV dbSNP153 33..33 33 - - - 78254 RMVar_ID_78254 Human_SNP_ID_675417624 m1A Human chr20 + 17627635 17627635 17627635 GAGCTGCCCGTGGAGGCCACTCAGCTCCTCGCATTTGCTGCGCACCTCCGCCTCGGAGGACTGTA GAGCTGCCCGTGGAGGCCACTCAGCTCCTCGCGTTTGCTGCGCACCTCCGCCTCGGAGGACTGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:17627466..17627718 26863196 MeRIP-seq:(Medium) rs1187064495 Functional Loss SNV dbSNP153 33..33 33 - - - 78255 RMVar_ID_78255 Human_SNP_ID_675418471 m1A Human chr20 - 17629903 17629903 17629903 CCTGCAGAAGCGCCTGGACGAGGTCAGCCGGGAGCTGTGCCACACGCAGAGCAGCCACGCCAGCC CCTGCAGAAGCGCCTGGACGAGGTCAGCCGGGGGCTGTGCCACACGCAGAGCAGCCACGCCAGCC T C RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:17629801..17629950;chr20:17629761..17629910 26863196 MeRIP-seq:(Medium) rs1429139019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62784,Human_RBP_ID_926654,Human_RBP_ID_22452921 Human_Splice_Rec_2063306,Human_Splice_Rec_2063307,Human_Splice_Rec_2063348,Human_Splice_Rec_2063349,Human_Splice_Rec_2063396,Human_Splice_Rec_2063397,Human_Splice_Rec_2063442,Human_Splice_Rec_2063443,Human_Splice_Rec_2063488,Human_Splice_Rec_2063489,Human_Splice_Rec_2063532,Human_Splice_Rec_2063533,Human_Splice_Rec_2063566,Human_Splice_Rec_2063567 Human_miRNA_ID_2396310,Human_miRNA_ID_2908737,Human_miRNA_ID_3027577 RMVar_hsa_circ_91274,RMVar_hsa_circ_14243,RMVar_hsa_circ_208859,RMVar_hsa_circ_341860,RMVar_hsa_circ_366076 78256 RMVar_ID_78256 Human_SNP_ID_675418478 m1A Human chr20 - 17629915 17629915 17629915 GAGTGAGGAGGCCCTGCAGAAGCGCCTGGACGAGGTCAGCCGGGAGCTGTGCCACACGCAGAGCA GAGTGAGGAGGCCCTGCAGAAGCGCCTGGACGGGGTCAGCCGGGAGCTGTGCCACACGCAGAGCA T C RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17629864..17630011 26863196 MeRIP-seq:(Medium) rs1215598974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62784,Human_RBP_ID_926654,Human_RBP_ID_22452921,Human_RBP_ID_26342355 Human_Splice_Rec_2063306,Human_Splice_Rec_2063307,Human_Splice_Rec_2063348,Human_Splice_Rec_2063349,Human_Splice_Rec_2063396,Human_Splice_Rec_2063397,Human_Splice_Rec_2063442,Human_Splice_Rec_2063443,Human_Splice_Rec_2063488,Human_Splice_Rec_2063489,Human_Splice_Rec_2063532,Human_Splice_Rec_2063533,Human_Splice_Rec_2063566,Human_Splice_Rec_2063567 RMVar_hsa_circ_91274,RMVar_hsa_circ_14243,RMVar_hsa_circ_208859,RMVar_hsa_circ_341860,RMVar_hsa_circ_366076 78257 RMVar_ID_78257 Human_SNP_ID_675418489 m1A Human chr20 - 17629952 17629952 17629952 CCCACTCCCCTGCCCGTCCCCAGGCGTCCCACAGGGAGAGTGAGGAGGCCCTGCAGAAGCGCCTG CCCACTCCCCTGCCCGTCCCCAGGCGTCCCACCGGGAGAGTGAGGAGGCCCTGCAGAAGCGCCTG T G RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:17624576..17641455 32194978 MeRIP-seq:(Medium) rs780537172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22452922 Human_Splice_Rec_2063306,Human_Splice_Rec_2063348,Human_Splice_Rec_2063396,Human_Splice_Rec_2063442,Human_Splice_Rec_2063488,Human_Splice_Rec_2063532,Human_Splice_Rec_2063566 RMVar_hsa_circ_91274,RMVar_hsa_circ_14243,RMVar_hsa_circ_208859,RMVar_hsa_circ_341860,RMVar_hsa_circ_366076 78258 RMVar_ID_78258 Human_SNP_ID_675419472 m1A Human chr20 + 17633508 17633508 17633508 TGCTTCTCGAAGGCAGCTGCCTTGGCTTCCAGAGCTTTCCGCTGCTGCTCATCTTGCCGCACAGC TGCTTCTCGAAGGCAGCTGCCTTGGCTTCCAGCGCTTTCCGCTGCTGCTCATCTTGCCGCACAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17633423..17633600 26863196 MeRIP-seq:(Medium) rs1261543140 Functional Loss SNV dbSNP153 33..33 33 - - - 78259 RMVar_ID_78259 Human_SNP_ID_675419480 m1A Human chr20 - 17633518 17633518 17633518 GAAGTCAGAGGCTGTGCGGCAAGATGAGCAGCAGCGGAAAGCTCTGGAAGCCAAGGCAGCTGCCT GAAGTCAGAGGCTGTGCGGCAAGATGAGCAGCGGCGGAAAGCTCTGGAAGCCAAGGCAGCTGCCT T C RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:17633422..17633578 26863196 MeRIP-seq:(Medium) rs755503466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5594861,Human_RBP_ID_9388725,Human_RBP_ID_19003817 Human_Splice_Rec_2063304,Human_Splice_Rec_2063305,Human_Splice_Rec_2063346,Human_Splice_Rec_2063347,Human_Splice_Rec_2063394,Human_Splice_Rec_2063395,Human_Splice_Rec_2063440,Human_Splice_Rec_2063441,Human_Splice_Rec_2063486,Human_Splice_Rec_2063487,Human_Splice_Rec_2063530,Human_Splice_Rec_2063531,Human_Splice_Rec_2063564,Human_Splice_Rec_2063565 Human_miRNA_ID_2826172,Human_miRNA_ID_2860145 RMVar_hsa_circ_91274,RMVar_hsa_circ_14243,RMVar_hsa_circ_208859,RMVar_hsa_circ_341860,RMVar_hsa_circ_366076,RMVar_hsa_circ_2068,RMVar_hsa_circ_65700 78260 RMVar_ID_78260 Human_SNP_ID_675426497 m1A Human chr20 + 17658846 17658846 17658846 TTTGTAATACCCTCTACCTTTGTGCCCTGATTAGCAACCGAATCTGCCTTTTTGCCCTGGATGGG TTTGTAATACCCTCTACCTTTGTGCCCTGATTTGCAACCGAATCTGCCTTTTTGCCCTGGATGGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:17658801..17658875 26863196 MeRIP-seq:(Medium) rs764805673 Functional Loss SNV dbSNP153 33..33 33 - - - 78261 RMVar_ID_78261 Human_SNP_ID_675426520 m1A Human chr20 - 17658905 17658905 17658905 GGGCTCAGGGCAAAAAGGCAGAAAGGAGTCCCAACCAAGGCAAAAAAGGAGAGGGAGCTCCCATC GGGCTCAGGGCAAAAAGGCAGAAAGGAGTCCCCACCAAGGCAAAAAAGGAGAGGGAGCTCCCATC T G RRBP1 Ensembl:ENSG00000125844 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:17658576..17659175 26863196 MeRIP-seq:(Medium) rs1568781175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62788 RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_347823,RMVar_hsa_circ_356409 78262 RMVar_ID_78262 Human_SNP_ID_675426717 m1A Human chr20 - 17659231 17659231 17659231 CCAGAATCAGGGCAAAAAGGCCGAGGGGGCCCAGAACCAGGGCAAGAAGGCCGAGGGGGCCCAGA CCAGAATCAGGGCAAAAAGGCCGAGGGGGCCCCGAACCAGGGCAAGAAGGCCGAGGGGGCCCAGA T G RRBP1 Ensembl:ENSG00000125844 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs202069077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_865210 GWAS_ID_9333 RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_347823,RMVar_hsa_circ_356409 78263 RMVar_ID_78263 Human_SNP_ID_675427028 m1A Human chr20 - 17659765 17659765 17659765 CCAAGGGAAAAAGGCAGAGGGAACCCCAAACCAAGGCAAAAAGGCAGAAGGAACCCCAAACCAAG CCAAGGGAAAAAGGCAGAGGGAACCCCAAACCGAGGCAAAAAGGCAGAAGGAACCCCAAACCAAG T C RRBP1 Ensembl:ENSG00000125844 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:17659512..17659952 26863196 MeRIP-seq:(Medium) rs1568782626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354018 RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_347823,RMVar_hsa_circ_356409 78264 RMVar_ID_78264 Human_SNP_ID_675427058 m1A Human chr20 - 17659825 17659825 17659825 CCAGGGCAGAAAGGCAGAGGGAACCCCAAACCAGGGCAAAAAGACAGAGGGAACCCCAAACCAAG CCAGGGCAGAAAGGCAGAGGGAACCCCAAACCGGGGCAAAAAGACAGAGGGAACCCCAAACCAAG T C RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:17659776..17659875 26863196 MeRIP-seq:(Medium) rs1000429378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831571 RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_347823,RMVar_hsa_circ_356409 78265 RMVar_ID_78265 Human_SNP_ID_675432937 m1A Human chr20 + 17682160 17682160 17682160 GAAACCGCCCCCGAGCAGCTGTAGACGCTGCGACCCTGACGCCGCCCGCCCCGTCTGCCGTCCGC GAAACCGCCCCCGAGCAGCTGTAGACGCTGCGCCCCTGACGCCGCCCGCCCCGTCTGCCGTCCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:17682061..17682187 26863410 MeRIP-seq:(Medium) rs991791499 Functional Loss SNV dbSNP153 33..33 33 - - - 78266 RMVar_ID_78266 Human_SNP_ID_675432954 m1A Human chr20 - 17682188 17682188 17682188 GCGCGCACGCAGCCAGCGAGCGGCCGGAGCGGACGGCAGACGGGGCGGGCGGCGTCAGGGTCGCA GCGCGCACGCAGCCAGCGAGCGGCCGGAGCGGGCGGCAGACGGGGCGGGCGGCGTCAGGGTCGCA T C RRBP1 Ensembl:ENSG00000125844 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:17681995..17682301;chr20:17682003..17682300;chr20:17681980..17682322;chr20:17681988..17682284 26863196 MeRIP-seq:(Medium) rs1485538173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63584,Human_RBP_ID_4659259,Human_RBP_ID_9390148,Human_RBP_ID_22452934 78267 RMVar_ID_78267 Human_SNP_ID_675498174 m1A Human chr20 + 17941896 17941896 17941896 TTATAGTACAAACACCAGATGACTACCAGTGGAGTAACAGGGCAAAACAAAAACACAAACCCCAC TTATAGTACAAACACCAGATGACTACCAGTGGCGTAACAGGGCAAAACAAAAACACAAACCCCAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17941845..17941995 32194978 MeRIP-seq:(Medium) rs1191079596 Functional Loss SNV dbSNP153 33..33 33 - - - 78268 RMVar_ID_78268 Human_SNP_ID_675499743 m1A Human chr20 - 17947533 17947533 17947533 CAAAGACGTCAAGTTGGCTGAGGCACACCAGCAGGAGTGCTGCCAGAAATTTGAACAACTTTCCG CAAAGACGTCAAGTTGGCTGAGGCACACCAGCTGGAGTGCTGCCAGAAATTTGAACAACTTTCCG T A SNX5 Ensembl:ENSG00000089006 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17947487..17948931 32194978 MeRIP-seq:(Medium) rs994789511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559597,Human_RBP_ID_1926296,Human_RBP_ID_4661114,Human_RBP_ID_6981599,Human_RBP_ID_8528868,Human_RBP_ID_9388752,Human_RBP_ID_14042212,Human_RBP_ID_17512816,Human_RBP_ID_22255607,Human_RBP_ID_22999618,Human_RBP_ID_25594157 Human_Splice_Rec_2063619,Human_Splice_Rec_2063643,Human_Splice_Rec_2063667,Human_Splice_Rec_2063693,Human_Splice_Rec_2063699,Human_Splice_Rec_2063717 Human_miRNA_ID_272898,Human_miRNA_ID_2052882,Human_miRNA_ID_2513311,Human_miRNA_ID_2709291,Human_miRNA_ID_3056130 RMVar_hsa_circ_90919,RMVar_hsa_circ_208861,RMVar_hsa_circ_101264,RMVar_hsa_circ_119050,RMVar_hsa_circ_208862,RMVar_hsa_circ_274458,RMVar_hsa_circ_367212,RMVar_hsa_circ_372839,RMVar_hsa_circ_208863,RMVar_hsa_circ_17983,RMVar_hsa_circ_280877,RMVar_hsa_circ_312646,RMVar_hsa_circ_365936,RMVar_hsa_circ_208864,RMVar_hsa_circ_324891,RMVar_hsa_circ_282969,RMVar_hsa_circ_274234,RMVar_hsa_circ_208865,RMVar_hsa_circ_208867,RMVar_hsa_circ_208868,RMVar_hsa_circ_208866 78269 RMVar_ID_78269 Human_SNP_ID_675499744 m1A Human chr20 - 17947533 17947533 17947533 CAAAGACGTCAAGTTGGCTGAGGCACACCAGCAGGAGTGCTGCCAGAAATTTGAACAACTTTCCG CAAAGACGTCAAGTTGGCTGAGGCACACCAGCGGGAGTGCTGCCAGAAATTTGAACAACTTTCCG T C SNX5 Ensembl:ENSG00000089006 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17947487..17948931 32194978 MeRIP-seq:(Medium) rs994789511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559597,Human_RBP_ID_1926296,Human_RBP_ID_4661114,Human_RBP_ID_6981599,Human_RBP_ID_8528868,Human_RBP_ID_9388752,Human_RBP_ID_14042212,Human_RBP_ID_17512816,Human_RBP_ID_22255607,Human_RBP_ID_22999618,Human_RBP_ID_25594157 Human_Splice_Rec_2063619,Human_Splice_Rec_2063643,Human_Splice_Rec_2063667,Human_Splice_Rec_2063693,Human_Splice_Rec_2063699,Human_Splice_Rec_2063717 Human_miRNA_ID_272898,Human_miRNA_ID_2052882,Human_miRNA_ID_2513311,Human_miRNA_ID_2709291,Human_miRNA_ID_3056130 RMVar_hsa_circ_90919,RMVar_hsa_circ_208861,RMVar_hsa_circ_101264,RMVar_hsa_circ_119050,RMVar_hsa_circ_208862,RMVar_hsa_circ_274458,RMVar_hsa_circ_367212,RMVar_hsa_circ_372839,RMVar_hsa_circ_208863,RMVar_hsa_circ_17983,RMVar_hsa_circ_280877,RMVar_hsa_circ_312646,RMVar_hsa_circ_365936,RMVar_hsa_circ_208864,RMVar_hsa_circ_324891,RMVar_hsa_circ_282969,RMVar_hsa_circ_274234,RMVar_hsa_circ_208865,RMVar_hsa_circ_208867,RMVar_hsa_circ_208868,RMVar_hsa_circ_208866 78270 RMVar_ID_78270 Human_SNP_ID_675504091 m1A Human chr20 - 17961755 17961755 17961755 CAAAATCTTAGTTTCTTAGGCAGTGGAATGAAACATAACAAAACAAAATCCCTAGAGGCTAGGAA CAAAATCTTAGTTTCTTAGGCAGTGGAATGAAGCATAACAAAACAAAATCCCTAGAGGCTAGGAA T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6080918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559647,Human_RBP_ID_10010297,Human_RBP_ID_14043022,Human_RBP_ID_17967820,Human_RBP_ID_22999678,Human_RBP_ID_23895478,Human_RBP_ID_25628281 GWAS_ID_9334,GWAS_ID_9335,GWAS_ID_9336,GWAS_ID_9337,GWAS_ID_9338,GWAS_ID_9339,GWAS_ID_9340,GWAS_ID_9341,GWAS_ID_9342,GWAS_ID_9343,GWAS_ID_9344,GWAS_ID_9345,GWAS_ID_9346,GWAS_ID_9347,GWAS_ID_9348 78271 RMVar_ID_78271 Human_SNP_ID_675505907 m1A Human chr20 - 17967439 17967439 17967439 TGTTCATCTAGTAAGTAAATACCAGAGTTTCAAAGCGGCTGGATTGTTCCAACAAGGGTATCATT TGTTCATCTAGTAAGTAAATACCAGAGTTTCAGAGCGGCTGGATTGTTCCAACAAGGGTATCATT T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2295457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043418 78272 RMVar_ID_78272 Human_SNP_ID_675506336 m1A Human chr20 - 17968455 17968455 17968455 GGCGGCCCAGCTTCTTCTTTCCTCGCACAGCCAGGCGGCCCCTGCTCGAGTCCCGCGTCGCCATG GGCGGCCCAGCTTCTTCTTTCCTCGCACAGCCGGGCGGCCCCTGCTCGAGTCCCGCGTCGCCATG T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:17968376..17968800 26863410 MeRIP-seq:(Medium) rs1005323010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4636802,Human_RBP_ID_5384665,Human_RBP_ID_22255720 Human_Splice_Rec_2063623,Human_Splice_Rec_2063672,Human_Splice_Rec_2063673,Human_Splice_Rec_2063731,Human_Splice_Rec_2063747,Human_Splice_Rec_2063789,Human_Splice_Rec_2063795,Human_Splice_Rec_2063799,Human_Splice_Rec_2063801 78273 RMVar_ID_78273 Human_SNP_ID_675506433 m1A Human chr20 + 17968602 17968602 17968602 CCGGACTCCGCCACCATCCCAGCTGCCCCGGGAGCAGGCGAGCAGGGCGCCACGTGCTCCCCCAG CCGGACTCCGCCACCATCCCAGCTGCCCCGGGGGCAGGCGAGCAGGGCGCCACGTGCTCCCCCAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:17968551..17968775 26863196 MeRIP-seq:(Medium) rs1213331584 Functional Loss SNV dbSNP153 33..33 33 - - - 78274 RMVar_ID_78274 Human_SNP_ID_675506507 m1A Human chr20 + 17968728 17968728 17968728 CTACCCTTGCTCCGCTCCACGAGGAGGCCGCCAACCGCAGGGCCGCGACACGGACGGGAAGCAAC CTACCCTTGCTCCGCTCCACGAGGAGGCCGCCGACCGCAGGGCCGCGACACGGACGGGAAGCAAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:17968642..17968732 26863196 MeRIP-seq:(Medium) rs113330582 Functional Loss SNV dbSNP153 33..33 33 - - - 78275 RMVar_ID_78275 Human_SNP_ID_675506513 m1A Human chr20 + 17968743 17968743 17968743 TCCACGAGGAGGCCGCCAACCGCAGGGCCGCGACACGGACGGGAAGCAACGGACACTCTCCCAGC TCCACGAGGAGGCCGCCAACCGCAGGGCCGCGGCACGGACGGGAAGCAACGGACACTCTCCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:17968650..17968775;chr20:17968453..17968800 26863196 MeRIP-seq:(Medium) rs990631477 Functional Loss SNV dbSNP153 33..33 33 - - - 78276 RMVar_ID_78276 Human_SNP_ID_675506514 m1A Human chr20 + 17968743 17968743 17968743 TCCACGAGGAGGCCGCCAACCGCAGGGCCGCGACACGGACGGGAAGCAACGGACACTCTCCCAGC TCCACGAGGAGGCCGCCAACCGCAGGGCCGCGTCACGGACGGGAAGCAACGGACACTCTCCCAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:17968650..17968775;chr20:17968453..17968800 26863196 MeRIP-seq:(Medium) rs990631477 Functional Loss SNV dbSNP153 33..33 33 - - - 78277 RMVar_ID_78277 Human_SNP_ID_675512509 m1A Human chr20 + 17990528 17990528 17990528 CCCCAGGGTTCACCCAGAGGGGAAGGGGCTACATGCCCCCAGCTGTGTGCAGGGAGGACACATCA CCCCAGGGTTCACCCAGAGGGGAAGGGGCTACCTGCCCCCAGCTGTGTGCAGGGAGGACACATCA A C MGME1 Ensembl:ENSG00000125871 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17990425..17990625 32194978 MeRIP-seq:(Medium) rs543323042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150189,Human_RBP_ID_4661157,Human_RBP_ID_6982010,Human_RBP_ID_8204498,Human_RBP_ID_17967850,Human_RBP_ID_26821236 78278 RMVar_ID_78278 Human_SNP_ID_675512510 m1A Human chr20 + 17990528 17990528 17990528 CCCCAGGGTTCACCCAGAGGGGAAGGGGCTACATGCCCCCAGCTGTGTGCAGGGAGGACACATCA CCCCAGGGTTCACCCAGAGGGGAAGGGGCTACGTGCCCCCAGCTGTGTGCAGGGAGGACACATCA A G MGME1 Ensembl:ENSG00000125871 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17990425..17990625 32194978 MeRIP-seq:(Medium) rs543323042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150189,Human_RBP_ID_4661157,Human_RBP_ID_6982010,Human_RBP_ID_8204498,Human_RBP_ID_17967850,Human_RBP_ID_26821236 78279 RMVar_ID_78279 Human_SNP_ID_675550896 m1A Human chr20 - 18138014 18138014 18138014 GGTCCCACTGCTGCTTCACATGTACGCCGGCCACTGTGGCCGCCGTCAGCAGCACCGAGAGGCCC GGTCCCACTGCTGCTTCACATGTACGCCGGCCGCTGTGGCCGCCGTCAGCAGCACCGAGAGGCCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18137971..18142326 32194978 MeRIP-seq:(Medium) rs898594649 Functional Loss SNV dbSNP153 33..33 33 - - - 78280 RMVar_ID_78280 Human_SNP_ID_675552405 m1A Human chr20 + 18142723 18142723 18142723 ATCAGTCGGCATGATGACGAAGCCACGAGAACATCGACCTCAGAAGGACTGGAGGAAGGTGAAGT ATCAGTCGGCATGATGACGAAGCCACGAGAACGTCGACCTCAGAAGGACTGGAGGAAGGTGAAGT A G PET117,KAT14 Ensembl:ENSG00000232838,Ensembl:ENSG00000149474 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:18142672..18142829 32194978 MeRIP-seq:(Medium) rs760836622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14044090 RMVar_hsa_circ_96693,RMVar_hsa_circ_208888,RMVar_hsa_circ_208886,RMVar_hsa_circ_269728,RMVar_hsa_circ_208887 78281 RMVar_ID_78281 Human_SNP_ID_675557242 m1A Human chr20 + 18162533 18162533 18162533 GATAAAGCAGGAGGTAGAGAGTGAGGAGGAAAAACCCGACAGGATGGATATTGACAGTGAAGACA GATAAAGCAGGAGGTAGAGAGTGAGGAGGAAACACCCGACAGGATGGATATTGACAGTGAAGACA A C KAT14 Ensembl:ENSG00000149474 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:18162461..18162614 26863196 MeRIP-seq:(Medium) rs1283150937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60223,RMVar_hsa_circ_208889,RMVar_hsa_circ_89025,RMVar_hsa_circ_349153,RMVar_hsa_circ_289986,RMVar_hsa_circ_208891,RMVar_hsa_circ_368232 78282 RMVar_ID_78282 Human_SNP_ID_675593921 m1A Human chr20 + 18315502 18315502 18315502 GAAGTCTTAGGATTTGGAACAGTCAACTGTGGAGAGTGTGGACTGAGCTTCAGCAAGATGACAAA GAAGTCTTAGGATTTGGAACAGTCAACTGTGGCGAGTGTGGACTGAGCTTCAGCAAGATGACAAA A C ZNF133 Ensembl:ENSG00000125846 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18315452..18315553 32194978 MeRIP-seq:(Medium) rs559436586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1926446,Human_RBP_ID_9388788,Human_RBP_ID_14044551,Human_RBP_ID_17967894,Human_RBP_ID_18769099,Human_RBP_ID_23895783,Human_RBP_ID_26343404,Human_RBP_ID_27819579 Human_miRNA_ID_2657808 RMVar_hsa_circ_125956,RMVar_hsa_circ_208894,RMVar_hsa_circ_76967,RMVar_hsa_circ_208895,RMVar_hsa_circ_92467,RMVar_hsa_circ_96173,RMVar_hsa_circ_208898,RMVar_hsa_circ_208899 78283 RMVar_ID_78283 Human_SNP_ID_675594156 m1A Human chr20 - 18316248 18316248 18316248 GGCTGAAGCCCCGGCCACAGTCCTTGCACACAATGGGCTTCTCTCCTGAGTGTATGTTCTGGTGT GGCTGAAGCCCCGGCCACAGTCCTTGCACACAGTGGGCTTCTCTCCTGAGTGTATGTTCTGGTGT T C AL049646.1 Ensembl:ENSG00000230010 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18316199..18316299 32194978 MeRIP-seq:(Medium) rs1304343177 Functional Loss SNV dbSNP153 33..33 33 - - - 78284 RMVar_ID_78284 Human_SNP_ID_675629581 m1A Human chr20 - 18466964 18466964 18466964 GGTGAGAGGCTGGCGACTGGGTTGGGCGCGGCAGAGATGCATTAGGGGTCCCGATCCCGGGCCCC GGTGAGAGGCTGGCGACTGGGTTGGGCGCGGCGGAGATGCATTAGGGGTCCCGATCCCGGGCCCC T C DZANK1 Ensembl:ENSG00000089091 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:18466850..18467007 26863196 MeRIP-seq:(Medium) rs922731127 Functional Loss SNV dbSNP153 33..33 33 - - - 78285 RMVar_ID_78285 Human_SNP_ID_675639121 m1A Human chr20 + 18504832 18504832 18504832 AGCCGGTTCCACAGCGCGGCACCTGTACCTCCAGGGTGGCGCTGGGGTTGGCTCCATGACCAAGA AGCCGGTTCCACAGCGCGGCACCTGTACCTCCGGGGTGGCGCTGGGGTTGGCTCCATGACCAAGA A G RPS19P1 Ensembl:ENSG00000214612 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878914350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559832 78286 RMVar_ID_78286 Human_SNP_ID_675639973 m1A Human chr20 + 18507971 18507971 18507971 TGTTGCAGCTGTGGGTGAGGACGGCTCTAGCTAGGTGAGCGGCTCCGGCCAGGTGAGCGGGGCGC TGTTGCAGCTGTGGGTGAGGACGGCTCTAGCTGGGTGAGCGGCTCCGGCCAGGTGAGCGGGGCGC A G SEC23B Ensembl:ENSG00000101310 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:18507954..18508121 26863196 MeRIP-seq:(Medium) rs1388956633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659263,Human_RBP_ID_5323174,Human_RBP_ID_8852853,Human_RBP_ID_19107675 Human_Splice_Rec_2064407,Human_Splice_Rec_2064463,Human_Splice_Rec_2064501,Human_Splice_Rec_2064539,Human_Splice_Rec_2064541,Human_Splice_Rec_2064545 RMVar_hsa_circ_208912,RMVar_hsa_circ_86924 78287 RMVar_ID_78287 Human_SNP_ID_675642290 m1A Human chr20 - 18517292 18517292 18517292 ACTTTGTGAGATCCACCTCCTGCCCACAAAACATTGCTCGTAACTCCACTGCCTATCCCAAAACC ACTTTGTGAGATCCACCTCCTGCCCACAAAACGTTGCTCGTAACTCCACTGCCTATCCCAAAACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:18517271..18517435 26863196 MeRIP-seq:(Medium) rs1191325555 Functional Loss SNV dbSNP153 33..33 33 - - - 78288 RMVar_ID_78288 Human_SNP_ID_675643092 m1A Human chr20 + 18520377 18520377 18520377 GGCATTGAGCGGGGTAAGAGTGATTAGGTTTTAATGGGATAGTAATGGGCGTGTGATCGGTTGCC GGCATTGAGCGGGGTAAGAGTGATTAGGTTTTCATGGGATAGTAATGGGCGTGTGATCGGTTGCC A C SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18520357..18520514 26863196 MeRIP-seq:(Medium) rs968914575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208914,RMVar_hsa_circ_208912,RMVar_hsa_circ_86924,RMVar_hsa_circ_313479,RMVar_hsa_circ_342054,RMVar_hsa_circ_367282,RMVar_hsa_circ_319588,RMVar_hsa_circ_298477,RMVar_hsa_circ_61057,RMVar_hsa_circ_74624,RMVar_hsa_circ_208913,RMVar_hsa_circ_42572,RMVar_hsa_circ_367017 78289 RMVar_ID_78289 Human_SNP_ID_675643093 m1A Human chr20 + 18520377 18520377 18520377 GGCATTGAGCGGGGTAAGAGTGATTAGGTTTTAATGGGATAGTAATGGGCGTGTGATCGGTTGCC GGCATTGAGCGGGGTAAGAGTGATTAGGTTTTTATGGGATAGTAATGGGCGTGTGATCGGTTGCC A T SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18520357..18520514 26863196 MeRIP-seq:(Medium) rs968914575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208914,RMVar_hsa_circ_208912,RMVar_hsa_circ_86924,RMVar_hsa_circ_313479,RMVar_hsa_circ_342054,RMVar_hsa_circ_367282,RMVar_hsa_circ_319588,RMVar_hsa_circ_298477,RMVar_hsa_circ_61057,RMVar_hsa_circ_74624,RMVar_hsa_circ_208913,RMVar_hsa_circ_42572,RMVar_hsa_circ_367017 78290 RMVar_ID_78290 Human_SNP_ID_675643107 m1A Human chr20 - 18520418 18520418 18520418 CCAACCTTAACCCACAAGTATGGGATACCTCCACTCTCTCTGGCAACCGATCACACGCCCATTAC CCAACCTTAACCCACAAGTATGGGATACCTCCTCTCTCTCTGGCAACCGATCACACGCCCATTAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:18520367..18520583 26863196 MeRIP-seq:(Medium) rs1490037843 Functional Loss SNV dbSNP153 33..33 33 - - - 78291 RMVar_ID_78291 Human_SNP_ID_675643404 m1A Human chr20 + 18521597 18521597 18521597 GGAGGGCTAGTCGTGGAACGAAATGGTAAGCCAGGCCGGGTGTGAGGAGGGGAGGTGATAGAAAG GGAGGGCTAGTCGTGGAACGAAATGGTAAGCCGGGCCGGGTGTGAGGAGGGGAGGTGATAGAAAG A G SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18521568..18521760 26863196 MeRIP-seq:(Medium) rs980500966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208914,RMVar_hsa_circ_208912,RMVar_hsa_circ_86924,RMVar_hsa_circ_313479,RMVar_hsa_circ_342054,RMVar_hsa_circ_367282,RMVar_hsa_circ_319588,RMVar_hsa_circ_298477,RMVar_hsa_circ_61057,RMVar_hsa_circ_74624,RMVar_hsa_circ_208913,RMVar_hsa_circ_42572,RMVar_hsa_circ_367017 78292 RMVar_ID_78292 Human_SNP_ID_675643427 m1A Human chr20 + 18521673 18521673 18521673 GGGGAGCAGAGGCTGAGAAAGAATTGGGACCTAGCTTGGCCTGGTGAGGAGCAACCTGGGGAGAA GGGGAGCAGAGGCTGAGAAAGAATTGGGACCTTGCTTGGCCTGGTGAGGAGCAACCTGGGGAGAA A T SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:18521624..18521741 26863196 MeRIP-seq:(Medium) rs1035762255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8203742 RMVar_hsa_circ_208914,RMVar_hsa_circ_208912,RMVar_hsa_circ_86924,RMVar_hsa_circ_313479,RMVar_hsa_circ_342054,RMVar_hsa_circ_367282,RMVar_hsa_circ_319588,RMVar_hsa_circ_298477,RMVar_hsa_circ_61057,RMVar_hsa_circ_74624,RMVar_hsa_circ_208913,RMVar_hsa_circ_42572,RMVar_hsa_circ_367017 78293 RMVar_ID_78293 Human_SNP_ID_675655013 m1A Human chr20 - 18567522 18567522 18567522 CCAACACAGACCAGGTGCCGATCCCGTAGACCACCGACATCCGCCGGTACCAGGCCGTGAACTCA CCAACACAGACCAGGTGCCGATCCCGTAGACCGCCGACATCCGCCGGTACCAGGCCGTGAACTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:18567471..18567578 26863196 MeRIP-seq:(Medium) rs944728155 Functional Loss SNV dbSNP153 33..33 33 - - - 78294 RMVar_ID_78294 Human_SNP_ID_675655014 m1A Human chr20 - 18567522 18567522 18567522 CCAACACAGACCAGGTGCCGATCCCGTAGACCACCGACATCCGCCGGTACCAGGCCGTGAACTCA CCAACACAGACCAGGTGCCGATCCCGTAGACCCCCGACATCCGCCGGTACCAGGCCGTGAACTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:18567471..18567578 26863196 MeRIP-seq:(Medium) rs944728155 Functional Loss SNV dbSNP153 33..33 33 - - - 78295 RMVar_ID_78295 Human_SNP_ID_675655038 m1A Human chr20 + 18567581 18567581 18567581 TGTTGGGCTCACTGCTTTACTATAGCCGGACAATGGCGAAGTCGTCAGGTAGGGCTCTTCGGCGG TGTTGGGCTCACTGCTTTACTATAGCCGGACAGTGGCGAAGTCGTCAGGTAGGGCTCTTCGGCGG A G SMIM26,AL121900.1 Ensembl:ENSG00000232388,Ensembl:ENSG00000284776 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18567451..18587948 32194978 MeRIP-seq:(Medium) rs935914302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559859,Human_RBP_ID_1024969,Human_RBP_ID_1593579,Human_RBP_ID_1926547,Human_RBP_ID_4659684,Human_RBP_ID_6982637,Human_RBP_ID_17396540,Human_RBP_ID_22453334,Human_RBP_ID_26820707 Human_Splice_Rec_2064637,Human_Splice_Rec_2064639,Human_Splice_Rec_2064641,Human_Splice_Rec_2064643 78296 RMVar_ID_78296 Human_SNP_ID_675661570 m1A Human chr20 + 18593743 18593743 18593743 CCCTTTTGGTTCCTTTCTAGTTGGAGGAGAGCAGATTAGTGCCATTGGAAGGGGCATATGTGTGT CCCTTTTGGTTCCTTTCTAGTTGGAGGAGAGCCGATTAGTGCCATTGGAAGGGGCATATGTGTGT A C DTD1,AL121900.1 Ensembl:ENSG00000125821,Ensembl:ENSG00000284776 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18587940..18593866 26863196 MeRIP-seq:(Medium) rs907384808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559880,Human_RBP_ID_4659686 Human_Splice_Rec_2064644,Human_Splice_Rec_2064645,Human_Splice_Rec_2064652,Human_Splice_Rec_2064653,Human_Splice_Rec_2064664,Human_Splice_Rec_2064665,Human_Splice_Rec_2064672,Human_Splice_Rec_2064673 RMVar_hsa_circ_208935,RMVar_hsa_circ_303187,RMVar_hsa_circ_314133,RMVar_hsa_circ_208936 78297 RMVar_ID_78297 Human_SNP_ID_675661597 m1A Human chr20 + 18593820 18593820 18593820 CCCTGGAGGATACGCAGAAGGAACTGGAACACATGTAAGATGCATTTCTGTCATTGCTGTTTGAG CCCTGGAGGATACGCAGAAGGAACTGGAACACGTGTAAGATGCATTTCTGTCATTGCTGTTTGAG A G DTD1,AL121900.1 Ensembl:ENSG00000125821,Ensembl:ENSG00000284776 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18593776..18628228 32194978 MeRIP-seq:(Medium) rs1288313914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17659231 Human_Splice_Rec_2064644,Human_Splice_Rec_2064645,Human_Splice_Rec_2064652,Human_Splice_Rec_2064653,Human_Splice_Rec_2064664,Human_Splice_Rec_2064665,Human_Splice_Rec_2064672,Human_Splice_Rec_2064673 RMVar_hsa_circ_208935,RMVar_hsa_circ_303187,RMVar_hsa_circ_314133,RMVar_hsa_circ_208936 78298 RMVar_ID_78298 Human_SNP_ID_675672341 m1A Human chr20 - 18638446 18638446 18638446 CTAGCGCTTGCACCTAAGGGGACTTCTAGCCAACAGCATTCTCTACACCTAACCCTGTTTGATTT CTAGCGCTTGCACCTAAGGGGACTTCTAGCCAGCAGCATTCTCTACACCTAACCCTGTTTGATTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:18638437..18638622 26863196 MeRIP-seq:(Medium) rs1040430120 Functional Loss SNV dbSNP153 33..33 33 - - - 78299 RMVar_ID_78299 Human_SNP_ID_675674430 m1A Human chr20 - 18647507 18647507 18647507 CCAAGCTTTCAGACCCAGCTGCCTCTTCCTCAACCTTCGAGATGCAACTAAGACATCTGTTCTGT CCAAGCTTTCAGACCCAGCTGCCTCTTCCTCAGCCTTCGAGATGCAACTAAGACATCTGTTCTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18647504..18647659 26863196 MeRIP-seq:(Medium) rs959206572 Functional Loss SNV dbSNP153 33..33 33 - - - 78300 RMVar_ID_78300 Human_SNP_ID_675697359 m1A Human chr20 + 18745951 18745951 18745951 GGAAGCAGATAGGCCCATTAGGAGGTGATTGCAGAAGTCCAGAGAAAAAATTATAGTAGGAACAG GGAAGCAGATAGGCCCATTAGGAGGTGATTGCGGAAGTCCAGAGAAAAAATTATAGTAGGAACAG A G DTD1 Ensembl:ENSG00000125821 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:18745949..18746077 26863196 MeRIP-seq:(Medium) rs79737297 Functional Loss SNV dbSNP153 33..33 33 - - - 78301 RMVar_ID_78301 Human_SNP_ID_675999447 m1A Human chr20 + 19975426 19975426 19975426 ACCAACAGCAGCCTGGAGGACTACGAGGGGGAAAGTGACCAAGAGACCATGGCGCCCCCCATCAA ACCAACAGCAGCCTGGAGGACTACGAGGGGGAGAGTGACCAAGAGACCATGGCGCCCCCCATCAA A G RIN2 Ensembl:ENSG00000132669 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:19975377..19975530 32194978 MeRIP-seq:(Medium) rs184553773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111672,RMVar_hsa_circ_127553,RMVar_hsa_circ_208947,RMVar_hsa_circ_75817,RMVar_hsa_circ_208949,RMVar_hsa_circ_67425,RMVar_hsa_circ_6525,RMVar_hsa_circ_113006,RMVar_hsa_circ_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208953,RMVar_hsa_circ_278701,RMVar_hsa_circ_208955,RMVar_hsa_circ_23109,RMVar_hsa_circ_208954,RMVar_hsa_circ_321490,RMVar_hsa_circ_208956 78302 RMVar_ID_78302 Human_SNP_ID_675999452 m1A Human chr20 + 19975442 19975442 19975442 AGGACTACGAGGGGGAAAGTGACCAAGAGACCATGGCGCCCCCCATCAAGTCCAAAAAGAAAAGG AGGACTACGAGGGGGAAAGTGACCAAGAGACCGTGGCGCCCCCCATCAAGTCCAAAAAGAAAAGG A G RIN2 Ensembl:ENSG00000132669 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:19975395..19975514 26863196 MeRIP-seq:(Medium) rs1459259971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111672,RMVar_hsa_circ_127553,RMVar_hsa_circ_208947,RMVar_hsa_circ_75817,RMVar_hsa_circ_208949,RMVar_hsa_circ_67425,RMVar_hsa_circ_6525,RMVar_hsa_circ_113006,RMVar_hsa_circ_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208953,RMVar_hsa_circ_278701,RMVar_hsa_circ_208955,RMVar_hsa_circ_23109,RMVar_hsa_circ_208954,RMVar_hsa_circ_321490,RMVar_hsa_circ_208956 78303 RMVar_ID_78303 Human_SNP_ID_471335511 m1A Human chr11 + 70203450 70203450 70203450 CGGAGGGCCGGGCCGCAGCCCCGGCCGCTTGCAGACCCCGCCATGGACCCGTTCCTGGTGCTGCT CGGAGGGCCGGGCCGCAGCCCCGGCCGCTTGCCGACCCCGCCATGGACCCGTTCCTGGTGCTGCT A C FADD Ensembl:ENSG00000168040 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:70203351..70203500 26863410 MeRIP-seq:(Medium) rs1325244763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866060,Human_RBP_ID_4185237,Human_RBP_ID_5436833,Human_RBP_ID_5490252,Human_RBP_ID_22035751 78304 RMVar_ID_78304 Human_SNP_ID_471336619 m1A Human chr11 - 70207039 70207039 70207039 CACGGCCAACCAGGTCTCCCCACCCCCACCCCAGCCATGCCTCTCCCCACCACAGCACCCCGCCT CACGGCCAACCAGGTCTCCCCACCCCCACCCCCGCCATGCCTCTCCCCACCACAGCACCCCGCCT T G AP000879.1 Ensembl:ENSG00000254721 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70206991..70207128 26863196 MeRIP-seq:(Medium) rs1305570879 Functional Loss SNV dbSNP153 33..33 33 - - - 78305 RMVar_ID_78305 Human_SNP_ID_471353235 m1A Human chr11 - 70270377 70270377 70270377 GCAGGGACGCCGGAGGCCTTTGCTGAGTGTCTACCGCGCCTCGAGTTCTGAGCTGGACGCGTCCG GCAGGGACGCCGGAGGCCTTTGCTGAGTGTCTGCCGCGCCTCGAGTTCTGAGCTGGACGCGTCCG T C lnc-SHANK2-9 RNACentral:URS0000D5CD50 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70270329..70270473 26863196 MeRIP-seq:(Medium) rs1028740085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23518765 78306 RMVar_ID_78306 Human_SNP_ID_471353439 m1A Human chr11 - 70270766 70270766 70270766 CCCCACGCCGCGGCCCCGGGGCCCGCCGCCCCAGTCACTAAGGCCGGCCCGCGGCCGGACACTGG CCCCACGCCGCGGCCCCGGGGCCCGCCGCCCCCGTCACTAAGGCCGGCCCGCGGCCGGACACTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70270725..70271105 26863196 MeRIP-seq:(Medium) rs1391840808 Functional Loss SNV dbSNP153 33..33 33 - - - 78307 RMVar_ID_78307 Human_SNP_ID_471353464 m1A Human chr11 + 70270810 70270810 70270810 CCCCGGGGCCGCGGCGTGGGGCGGGCAGGCGGACGCCGGCCGCGGGCTGCTTTCGTCGGCTCCCA CCCCGGGGCCGCGGCGTGGGGCGGGCAGGCGGCCGCCGGCCGCGGGCTGCTTTCGTCGGCTCCCA A C PPFIA1 Ensembl:ENSG00000131626 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:70270701..70270900 26863410 MeRIP-seq:(Medium) rs1040961021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227612,Human_RBP_ID_4184296,Human_RBP_ID_5138713,Human_RBP_ID_5235282,Human_RBP_ID_8773825,Human_RBP_ID_9276000,Human_RBP_ID_18478096,Human_RBP_ID_26775679 78308 RMVar_ID_78308 Human_SNP_ID_471353494 m1A Human chr11 + 70270912 70270912 70270912 CGGAGCCTCCTCGCCCGCTCCCGCCGGCGAGCAAGGTAAGGGAGCGGGACACTGAGGCAGGCTCG CGGAGCCTCCTCGCCCGCTCCCGCCGGCGAGCGAGGTAAGGGAGCGGGACACTGAGGCAGGCTCG A G PPFIA1 Ensembl:ENSG00000131626 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:70270773..70270925;chr11:70270726..70271245 26863196 MeRIP-seq:(Medium) rs1035954862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227613,Human_RBP_ID_4185239,Human_RBP_ID_18612208,Human_RBP_ID_26767963 Human_Splice_Rec_1270375,Human_Splice_Rec_1270425,Human_Splice_Rec_1270471 78309 RMVar_ID_78309 Human_SNP_ID_471353876 m1A Human chr11 - 70272128 70272128 70272128 GACCCAGGCTACAGTAATTAAGCTCAGAATACAGGTTCCCACAAATATGCAACTTTACAGGTATC GACCCAGGCTACAGTAATTAAGCTCAGAATACGGGTTCCCACAAATATGCAACTTTACAGGTATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70272126..70272281 26863196 MeRIP-seq:(Medium) rs1372006251 Functional Loss SNV dbSNP153 33..33 33 - - - 78310 RMVar_ID_78310 Human_SNP_ID_471362228 m1A Human chr11 + 70302353 70302353 70302353 GTGGGAGAAGGGTGGCTGACCAGGAAACAGGAAAGGCATGGAGGGCTGTGAGCTCACAGGAAGGT GTGGGAGAAGGGTGGCTGACCAGGAAACAGGACAGGCATGGAGGGCTGTGAGCTCACAGGAAGGT A C PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:70302343..70302462;chr11:70302216..70302513 26863196 MeRIP-seq:(Medium) rs931581184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11698793 RMVar_hsa_circ_53935,RMVar_hsa_circ_73245,RMVar_hsa_circ_368450,RMVar_hsa_circ_371381,RMVar_hsa_circ_351649,RMVar_hsa_circ_61701,RMVar_hsa_circ_151361,RMVar_hsa_circ_47213,RMVar_hsa_circ_151362,RMVar_hsa_circ_151360 78311 RMVar_ID_78311 Human_SNP_ID_471365122 m1A Human chr11 - 70314230 70314230 70314230 TCTGCTAAACCCAAAGGCCAGCTCCAGTCCTCATCTACTGGGTAGCCTCTGACTGTTCACCCCCA TCTGCTAAACCCAAAGGCCAGCTCCAGTCCTCTTCTACTGGGTAGCCTCTGACTGTTCACCCCCA T A AP002336.2 Ensembl:ENSG00000254604 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70314226..70314323 26863196 MeRIP-seq:(Medium) rs1328686984 Functional Loss SNV dbSNP153 33..33 33 - - - 78312 RMVar_ID_78312 Human_SNP_ID_471365123 m1A Human chr11 - 70314230 70314230 70314230 TCTGCTAAACCCAAAGGCCAGCTCCAGTCCTCATCTACTGGGTAGCCTCTGACTGTTCACCCCCA TCTGCTAAACCCAAAGGCCAGCTCCAGTCCTCGTCTACTGGGTAGCCTCTGACTGTTCACCCCCA T C AP002336.2 Ensembl:ENSG00000254604 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70314226..70314323 26863196 MeRIP-seq:(Medium) rs1328686984 Functional Loss SNV dbSNP153 33..33 33 - - - 78313 RMVar_ID_78313 Human_SNP_ID_471365282 m1A Human chr11 - 70314869 70314869 70314869 TCCTGAGGCCTCCCCAGCCATGCGGAACTGTGAGTCAATTAAACCTTTCCTTTATGAATTACCCA TCCTGAGGCCTCCCCAGCCATGCGGAACTGTGGGTCAATTAAACCTTTCCTTTATGAATTACCCA T C AP002336.2 Ensembl:ENSG00000254604 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70314867..70314967 26863196 MeRIP-seq:(Medium) rs1018317240 Functional Loss SNV dbSNP153 33..33 33 - - - 78314 RMVar_ID_78314 Human_SNP_ID_471370477 m1A Human chr11 + 70335512 70335512 70335512 CTCACCCTGTTGGTCCTTGTGCTTTTAAAATAATGATCGAGGATTTACGTGAGGTTTATAAGACT CTCACCCTGTTGGTCCTTGTGCTTTTAAAATAGTGATCGAGGATTTACGTGAGGTTTATAAGACT A G PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70335511..70335580 26863196 MeRIP-seq:(Medium) rs1425890159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_544,RMVar_hsa_circ_371381,RMVar_hsa_circ_351649,RMVar_hsa_circ_61701,RMVar_hsa_circ_355170,RMVar_hsa_circ_151361,RMVar_hsa_circ_47213,RMVar_hsa_circ_365943,RMVar_hsa_circ_151360,RMVar_hsa_circ_364551,RMVar_hsa_circ_55583,RMVar_hsa_circ_67211,RMVar_hsa_circ_93880,RMVar_hsa_circ_151365,RMVar_hsa_circ_68798,RMVar_hsa_circ_151367,RMVar_hsa_circ_77669,RMVar_hsa_circ_151366,RMVar_hsa_circ_79719,RMVar_hsa_circ_151368,RMVar_hsa_circ_151369,RMVar_hsa_circ_112609,RMVar_hsa_circ_281812,RMVar_hsa_circ_333717,RMVar_hsa_circ_273901,RMVar_hsa_circ_59625,RMVar_hsa_circ_16914,RMVar_hsa_circ_50595,RMVar_hsa_circ_95810,RMVar_hsa_circ_151371,RMVar_hsa_circ_151372,RMVar_hsa_circ_319492,RMVar_hsa_circ_151374,RMVar_hsa_circ_151373,RMVar_hsa_circ_265784 78315 RMVar_ID_78315 Human_SNP_ID_471371382 m1A Human chr11 - 70339212 70339212 70339212 TGGTGCTGTAGGAGTCTGTGTGGCCGTCTGCCATGGGGAACCTGAAATCTGGGACACTGCCCAAG TGGTGCTGTAGGAGTCTGTGTGGCCGTCTGCCGTGGGGAACCTGAAATCTGGGACACTGCCCAAG T C AP002336.2 Ensembl:ENSG00000254604 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:70338444..70339262 32194978 MeRIP-seq:(Medium) rs1306333971 Functional Loss SNV dbSNP153 33..33 33 - - - 78316 RMVar_ID_78316 Human_SNP_ID_471386385 m1A Human chr11 + 70397328 70397328 70397328 TTCCGCCACCCGCACTTCCAATTCATCCTCACATCTGACAGTTTAGCTTTCTAAATGCCTCTTGC TTCCGCCACCCGCACTTCCAATTCATCCTCACTTCTGACAGTTTAGCTTTCTAAATGCCTCTTGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70397326..70397433 26863196 MeRIP-seq:(Medium) rs1161014898 Functional Loss SNV dbSNP153 33..33 33 - - - 78317 RMVar_ID_78317 Human_SNP_ID_471386402 m1A Human chr11 - 70397409 70397409 70397409 GGAGAAGGGCCAGGTAGAGCCTAATGTAGCCAATTCGGGCAGACCGCTGGTGGCAGGTAAGATGG GGAGAAGGGCCAGGTAGAGCCTAATGTAGCCAGTTCGGGCAGACCGCTGGTGGCAGGTAAGATGG T C AP000487.1 Ensembl:ENSG00000246889 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:70397287..70397463 26863196 MeRIP-seq:(Medium) rs572773028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5313772 78318 RMVar_ID_78318 Human_SNP_ID_471389228 m1A Human chr11 + 70407564 70407564 70407564 GAAGGAGCAAAGATGGGGTGCCAAGACGGTGCAGGGCTCCGGGCACCAGGAGCATATCAAGTAAG GAAGGAGCAAAGATGGGGTGCCAAGACGGTGCTGGGCTCCGGGCACCAGGAGCATATCAAGTAAG A T CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:70407472..70407647;chr11:70407480..70407679;chr11:70407301..70407665 26863196 MeRIP-seq:(Medium) rs1252489747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29556,Human_RBP_ID_871273,Human_RBP_ID_5110571,Human_RBP_ID_9362682,Human_RBP_ID_11700420,Human_RBP_ID_17804697,Human_RBP_ID_18972468,Human_RBP_ID_19050162 Human_Splice_Rec_1270864,Human_Splice_Rec_1270865,Human_Splice_Rec_1270896,Human_Splice_Rec_1270897,Human_Splice_Rec_1270928,Human_Splice_Rec_1270934,Human_Splice_Rec_1270935,Human_Splice_Rec_1270944,Human_Splice_Rec_1270945,Human_Splice_Rec_1270976,Human_Splice_Rec_1270977 Human_miRNA_ID_2380902,Human_miRNA_ID_3023916 RMVar_hsa_circ_1455,RMVar_hsa_circ_110058,RMVar_hsa_circ_294400,RMVar_hsa_circ_349366,RMVar_hsa_circ_357711,RMVar_hsa_circ_337161,RMVar_hsa_circ_279319,RMVar_hsa_circ_43748,RMVar_hsa_circ_65219,RMVar_hsa_circ_23191,RMVar_hsa_circ_31526,RMVar_hsa_circ_113866,RMVar_hsa_circ_151399,RMVar_hsa_circ_151400,RMVar_hsa_circ_151401,RMVar_hsa_circ_151398,RMVar_hsa_circ_64784,RMVar_hsa_circ_151402 78319 RMVar_ID_78319 Human_SNP_ID_471389234 m1A Human chr11 - 70407593 70407593 70407593 GGGCCCTCGGGAGGGTGGTGGCGACGCCTCTTACTTGATATGCTCCTGGTGCCCGGAGCCCTGCA GGGCCCTCGGGAGGGTGGTGGCGACGCCTCTTTCTTGATATGCTCCTGGTGCCCGGAGCCCTGCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:70407576..70407625 32194978 MeRIP-seq:(Medium) rs111344988 Functional Loss SNV dbSNP153 33..33 33 - - - 78320 RMVar_ID_78320 Human_SNP_ID_471389770 m1A Human chr11 - 70409794 70409794 70409794 ATGGAAGAGATGAAAATAGGAACAGATCAATAAAACAGACGTGCAGCTTTGCCTCCTGGTATGAT ATGGAAGAGATGAAAATAGGAACAGATCAATAGAACAGACGTGCAGCTTTGCCTCCTGGTATGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70409791..70409985 26863196 MeRIP-seq:(Medium) rs185782439 Functional Loss SNV dbSNP153 33..33 33 - - - 78321 RMVar_ID_78321 Human_SNP_ID_471391918 m1A Human chr11 + 70417064 70417064 70417064 CGGCAAGTATGGCGTGCAGGCCGACCGAGTAGACAAGAGCGCGGTGGGCTTCGACTACCAGGGCA CGGCAAGTATGGCGTGCAGGCCGACCGAGTAGCCAAGAGCGCGGTGGGCTTCGACTACCAGGGCA A C CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:70417001..70417100 32194978 MeRIP-seq:(Medium) rs757372494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402764,Human_RBP_ID_11700676,Human_RBP_ID_27804833 Human_Splice_Rec_1270872,Human_Splice_Rec_1270873,Human_Splice_Rec_1270904,Human_Splice_Rec_1270905,Human_Splice_Rec_1270952,Human_Splice_Rec_1270953,Human_Splice_Rec_1270984,Human_Splice_Rec_1270985,Human_Splice_Rec_1270989 Human_miRNA_ID_3114564 RMVar_hsa_circ_1455,RMVar_hsa_circ_110058,RMVar_hsa_circ_357711,RMVar_hsa_circ_337161,RMVar_hsa_circ_65219,RMVar_hsa_circ_23191,RMVar_hsa_circ_113866,RMVar_hsa_circ_151398,RMVar_hsa_circ_1579,RMVar_hsa_circ_151402,RMVar_hsa_circ_349586,RMVar_hsa_circ_42513,RMVar_hsa_circ_151404,RMVar_hsa_circ_72917,RMVar_hsa_circ_11242,RMVar_hsa_circ_151405,RMVar_hsa_circ_78621,RMVar_hsa_circ_273276,RMVar_hsa_circ_347554,RMVar_hsa_circ_47483,RMVar_hsa_circ_151406 78322 RMVar_ID_78322 Human_SNP_ID_471391919 m1A Human chr11 + 70417064 70417064 70417064 CGGCAAGTATGGCGTGCAGGCCGACCGAGTAGACAAGAGCGCGGTGGGCTTCGACTACCAGGGCA CGGCAAGTATGGCGTGCAGGCCGACCGAGTAGTCAAGAGCGCGGTGGGCTTCGACTACCAGGGCA A T CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:70417001..70417100 32194978 MeRIP-seq:(Medium) rs757372494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402764,Human_RBP_ID_11700676,Human_RBP_ID_27804833 Human_Splice_Rec_1270872,Human_Splice_Rec_1270873,Human_Splice_Rec_1270904,Human_Splice_Rec_1270905,Human_Splice_Rec_1270952,Human_Splice_Rec_1270953,Human_Splice_Rec_1270984,Human_Splice_Rec_1270985,Human_Splice_Rec_1270989 Human_miRNA_ID_3114564 RMVar_hsa_circ_1455,RMVar_hsa_circ_110058,RMVar_hsa_circ_357711,RMVar_hsa_circ_337161,RMVar_hsa_circ_65219,RMVar_hsa_circ_23191,RMVar_hsa_circ_113866,RMVar_hsa_circ_151398,RMVar_hsa_circ_1579,RMVar_hsa_circ_151402,RMVar_hsa_circ_349586,RMVar_hsa_circ_42513,RMVar_hsa_circ_151404,RMVar_hsa_circ_72917,RMVar_hsa_circ_11242,RMVar_hsa_circ_151405,RMVar_hsa_circ_78621,RMVar_hsa_circ_273276,RMVar_hsa_circ_347554,RMVar_hsa_circ_47483,RMVar_hsa_circ_151406 78323 RMVar_ID_78323 Human_SNP_ID_471395533 m1A Human chr11 + 70429152 70429152 70429152 GGCGGAAGGCGGAGGCGGAGAGAGCCCAGCGGATGGCCAAGGAGCGGCAGGAGCAGGAAGAGGCC GGCGGAAGGCGGAGGCGGAGAGAGCCCAGCGGGTGGCCAAGGAGCGGCAGGAGCAGGAAGAGGCC A G CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr11:70429047..70429243;chr11:70428998..70429238;chr11:70428991..70429251;chr11:70429001..70431275;chr11:70429101..70429200 26863196,32194978 MeRIP-seq:(Medium) rs769938933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226276,Human_RBP_ID_402774,Human_RBP_ID_806737,Human_RBP_ID_869205,Human_RBP_ID_3939624,Human_RBP_ID_9362689,Human_RBP_ID_18974527,Human_RBP_ID_22895576,Human_RBP_ID_26318939,Human_RBP_ID_26896634,Human_RBP_ID_27803771 Human_Splice_Rec_1270883,Human_Splice_Rec_1270915,Human_Splice_Rec_1270963,Human_Splice_Rec_1271013,Human_Splice_Rec_1271023,Human_Splice_Rec_1271035 Human_miRNA_ID_1809146,Human_miRNA_ID_2217972,Human_miRNA_ID_2393237 RMVar_hsa_circ_1306,RMVar_hsa_circ_357711,RMVar_hsa_circ_65219,RMVar_hsa_circ_23191,RMVar_hsa_circ_113866,RMVar_hsa_circ_151402,RMVar_hsa_circ_56209,RMVar_hsa_circ_305080,RMVar_hsa_circ_370853,RMVar_hsa_circ_284994,RMVar_hsa_circ_69320,RMVar_hsa_circ_151411,RMVar_hsa_circ_151412,RMVar_hsa_circ_22373 78324 RMVar_ID_78324 Human_SNP_ID_471395534 m1A Human chr11 + 70429152 70429152 70429152 GGCGGAAGGCGGAGGCGGAGAGAGCCCAGCGGATGGCCAAGGAGCGGCAGGAGCAGGAAGAGGCC GGCGGAAGGCGGAGGCGGAGAGAGCCCAGCGGTTGGCCAAGGAGCGGCAGGAGCAGGAAGAGGCC A T CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr11:70429047..70429243;chr11:70428998..70429238;chr11:70428991..70429251;chr11:70429001..70431275;chr11:70429101..70429200 26863196,32194978 MeRIP-seq:(Medium) rs769938933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226276,Human_RBP_ID_402774,Human_RBP_ID_806737,Human_RBP_ID_869205,Human_RBP_ID_3939624,Human_RBP_ID_9362689,Human_RBP_ID_18974527,Human_RBP_ID_22895576,Human_RBP_ID_26318939,Human_RBP_ID_26896634,Human_RBP_ID_27803771 Human_Splice_Rec_1270883,Human_Splice_Rec_1270915,Human_Splice_Rec_1270963,Human_Splice_Rec_1271013,Human_Splice_Rec_1271023,Human_Splice_Rec_1271035 Human_miRNA_ID_1809146,Human_miRNA_ID_2217972,Human_miRNA_ID_2393237 RMVar_hsa_circ_1306,RMVar_hsa_circ_357711,RMVar_hsa_circ_65219,RMVar_hsa_circ_23191,RMVar_hsa_circ_113866,RMVar_hsa_circ_151402,RMVar_hsa_circ_56209,RMVar_hsa_circ_305080,RMVar_hsa_circ_370853,RMVar_hsa_circ_284994,RMVar_hsa_circ_69320,RMVar_hsa_circ_151411,RMVar_hsa_circ_151412,RMVar_hsa_circ_22373 78325 RMVar_ID_78325 Human_SNP_ID_471396161 m1A Human chr11 - 70431277 70431277 70431277 ACGCTCATTCAAACACCAAAGACACCAACCTCATAGACGGGGCTCGAGGGCAGCCTCTCCTCGGT ACGCTCATTCAAACACCAAAGACACCAACCTCGTAGACGGGGCTCGAGGGCAGCCTCTCCTCGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:70431176..70431300 32194978 MeRIP-seq:(Medium) rs1467509527 Functional Loss SNV dbSNP153 33..33 33 - - - 78326 RMVar_ID_78326 Human_SNP_ID_471396795 m1A Human chr11 + 70433176 70433176 70433176 TGAGTGGGACGGAGCCGGAGCCCGTGTACAGCATGGAGGCCGCTGACTACCGAGAGGCCAGCAGC TGAGTGGGACGGAGCCGGAGCCCGTGTACAGCCTGGAGGCCGCTGACTACCGAGAGGCCAGCAGC A C CTTN Ensembl:ENSG00000085733 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:70433126..70433221 26863196 MeRIP-seq:(Medium) rs776585210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9006006,Human_RBP_ID_9276633,Human_RBP_ID_9362690,Human_RBP_ID_11701112,Human_RBP_ID_18974531,Human_RBP_ID_21883629 Human_Splice_Rec_1270886,Human_Splice_Rec_1270918,Human_Splice_Rec_1270966,Human_Splice_Rec_1271016,Human_Splice_Rec_1271026,Human_Splice_Rec_1271038 Human_miRNA_ID_2896709 RMVar_hsa_circ_1306,RMVar_hsa_circ_65219,RMVar_hsa_circ_113866,RMVar_hsa_circ_151402,RMVar_hsa_circ_56209,RMVar_hsa_circ_305080 78327 RMVar_ID_78327 Human_SNP_ID_471397729 m1A Human chr11 - 70435564 70435564 70435564 GTCTGGGACAGTCCTTCCTGCCTACCCGCCACAGGGCCGACCTGAGGCCTCGTGCTTGTCCTGGG GTCTGGGACAGTCCTTCCTGCCTACCCGCCACCGGGCCGACCTGAGGCCTCGTGCTTGTCCTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70435465..70435702 26863196 MeRIP-seq:(Medium) rs747805385 Functional Loss SNV dbSNP153 33..33 33 - - - 78328 RMVar_ID_78328 Human_SNP_ID_471397881 m1A Human chr11 + 70435929 70435929 70435929 CCTGCCCCGCGGGTCTCTGGATTGGGACGCACAGTGCAGTTGAGGTCTGCGTCGGGCTTGGCTTT CCTGCCCCGCGGGTCTCTGGATTGGGACGCACCGTGCAGTTGAGGTCTGCGTCGGGCTTGGCTTT A C CTTN Ensembl:ENSG00000085733 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70435880..70435969 26863196 MeRIP-seq:(Medium) rs1246948730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402810,Human_RBP_ID_1163373,Human_RBP_ID_4176846,Human_RBP_ID_6091247,Human_RBP_ID_11701181 Human_miRNA_ID_325314,Human_miRNA_ID_577113,Human_miRNA_ID_2205937 RMVar_hsa_circ_113866,RMVar_hsa_circ_151402 78329 RMVar_ID_78329 Human_SNP_ID_471397882 m1A Human chr11 + 70435929 70435929 70435929 CCTGCCCCGCGGGTCTCTGGATTGGGACGCACAGTGCAGTTGAGGTCTGCGTCGGGCTTGGCTTT CCTGCCCCGCGGGTCTCTGGATTGGGACGCACGGTGCAGTTGAGGTCTGCGTCGGGCTTGGCTTT A G CTTN Ensembl:ENSG00000085733 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:70435880..70435969 26863196 MeRIP-seq:(Medium) rs1246948730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_402810,Human_RBP_ID_1163373,Human_RBP_ID_4176846,Human_RBP_ID_6091247,Human_RBP_ID_11701181 Human_miRNA_ID_325314,Human_miRNA_ID_577113,Human_miRNA_ID_2205937 RMVar_hsa_circ_113866,RMVar_hsa_circ_151402 78330 RMVar_ID_78330 Human_SNP_ID_471397924 m1A Human chr11 - 70436077 70436077 70436077 GAGGGTTCCTGGCGGCTCACAGCAGAGCAGGCACTGCCTTCCTTCCCAAGGCCGAGAGGCCATGC GAGGGTTCCTGGCGGCTCACAGCAGAGCAGGCGCTGCCTTCCTTCCCAAGGCCGAGAGGCCATGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:70436026..70436150 32194978 MeRIP-seq:(Medium) rs1191020952 Functional Loss SNV dbSNP153 33..33 33 - - - 78331 RMVar_ID_78331 Human_SNP_ID_471638110 m1A Human chr11 + 71444107 71444107 71444107 GCATGTCCGGTGACGATGTCCACCACAGGGCCAGTCAGGGCGCAGCTGTACTGGTCACAAGCCAT GCATGTCCGGTGACGATGTCCACCACAGGGCCGGTCAGGGCGCAGCTGTACTGGTCACAAGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71444057..71444163 26863196 MeRIP-seq:(Medium) rs1790334 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_360,Clinvar_Rec_8585 GWAS_ID_9349,GWAS_ID_9350,GWAS_ID_9351,GWAS_ID_9352,GWAS_ID_9353 78332 RMVar_ID_78332 Human_SNP_ID_471638127 m1A Human chr11 - 71444142 71444142 71444142 TGCTGTTCGCCCCCTTCATCGTCTACTACTTCATCATGGCTTGTGACCAGTACAGCTGCGCCCTG TGCTGTTCGCCCCCTTCATCGTCTACTACTTCTTCATGGCTTGTGACCAGTACAGCTGCGCCCTG T A DHCR7 Ensembl:ENSG00000172893 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:71443962..71444227 26863196 MeRIP-seq:(Medium) rs104886032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31480,Human_RBP_ID_870336,Human_RBP_ID_8357966,Human_RBP_ID_18188597,Human_RBP_ID_22433851,Human_RBP_ID_22753741,Human_RBP_ID_27415784 Human_Splice_Rec_1271418,Human_Splice_Rec_1271434,Human_Splice_Rec_1271474,Human_Splice_Rec_1271484,Human_Splice_Rec_1271490,Human_Splice_Rec_1271502 Human_miRNA_ID_2779758 RMVar_hsa_circ_7064,RMVar_hsa_circ_123490,RMVar_hsa_circ_110251,RMVar_hsa_circ_151435,RMVar_hsa_circ_151436,RMVar_hsa_circ_366020,RMVar_hsa_circ_105003,RMVar_hsa_circ_151445,RMVar_hsa_circ_89551,RMVar_hsa_circ_151444,RMVar_hsa_circ_373810,RMVar_hsa_circ_151447,RMVar_hsa_circ_80597,RMVar_hsa_circ_151448 78333 RMVar_ID_78333 Human_SNP_ID_471638128 m1A Human chr11 - 71444142 71444142 71444142 TGCTGTTCGCCCCCTTCATCGTCTACTACTTCATCATGGCTTGTGACCAGTACAGCTGCGCCCTG TGCTGTTCGCCCCCTTCATCGTCTACTACTTCGTCATGGCTTGTGACCAGTACAGCTGCGCCCTG T C DHCR7 Ensembl:ENSG00000172893 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:71443962..71444227 26863196 MeRIP-seq:(Medium) rs104886032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31480,Human_RBP_ID_870336,Human_RBP_ID_8357966,Human_RBP_ID_18188597,Human_RBP_ID_22433851,Human_RBP_ID_22753741,Human_RBP_ID_27415784 Human_Splice_Rec_1271418,Human_Splice_Rec_1271434,Human_Splice_Rec_1271474,Human_Splice_Rec_1271484,Human_Splice_Rec_1271490,Human_Splice_Rec_1271502 Human_miRNA_ID_2779758 RMVar_hsa_circ_7064,RMVar_hsa_circ_123490,RMVar_hsa_circ_110251,RMVar_hsa_circ_151435,RMVar_hsa_circ_151436,RMVar_hsa_circ_366020,RMVar_hsa_circ_105003,RMVar_hsa_circ_151445,RMVar_hsa_circ_89551,RMVar_hsa_circ_151444,RMVar_hsa_circ_373810,RMVar_hsa_circ_151447,RMVar_hsa_circ_80597,RMVar_hsa_circ_151448 78334 RMVar_ID_78334 Human_SNP_ID_471639453 m1A Human chr11 - 71448721 71448721 71448721 GCCCCATTTGCCGAGGGGGAAACTGAGGCACGATGATCCAGGTGATGAGCCTGGCGCGTTCTCCG GCCCCATTTGCCGAGGGGGAAACTGAGGCACGGTGATCCAGGTGATGAGCCTGGCGCGTTCTCCG T C DHCR7 Ensembl:ENSG00000172893 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71448672..71448749 26863196 MeRIP-seq:(Medium) rs1398064903 Functional Loss SNV dbSNP153 33..33 33 - - - 78335 RMVar_ID_78335 Human_SNP_ID_471640598 m1A Human chr11 + 71453307 71453307 71453307 TGCCCAAGCGACTGCGGCCAGGATGGGCCGGAAGGTGACCGTGGCCACCTGCGCACTCAACCAGT TGCCCAAGCGACTGCGGCCAGGATGGGCCGGAGGGTGACCGTGGCCACCTGCGCACTCAACCAGT A G NADSYN1 Ensembl:ENSG00000172890 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71453257..71453322 26863196 MeRIP-seq:(Medium) rs776083387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184304,Human_RBP_ID_18417198,Human_RBP_ID_26318944 Human_Splice_Rec_1271505,Human_Splice_Rec_1271509,Human_Splice_Rec_1271549,Human_Splice_Rec_1271551,Human_Splice_Rec_1271563,Human_Splice_Rec_1271581,Human_Splice_Rec_1271589,Human_Splice_Rec_1271601,Human_Splice_Rec_1271607 RMVar_hsa_circ_84797,RMVar_hsa_circ_106445,RMVar_hsa_circ_120441,RMVar_hsa_circ_89510,RMVar_hsa_circ_151450,RMVar_hsa_circ_151452,RMVar_hsa_circ_151453,RMVar_hsa_circ_151451 78336 RMVar_ID_78336 Human_SNP_ID_471646373 m1A Human chr11 - 71474733 71474731 71474733 GGCCCTCACTAAGCACCCGGCTTACAGGGGAGAGCCAGGAGCAGGCGGGACCCCCGGGGGCTTCT GGCCCTCACTAAGCACCCGGCTTACAGGGGAG__CCAGGAGCAGGCGGGACCCCCGGGGGCTTCT GCT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:71474654..71474741 26863410 MeRIP-seq:(Medium) rs1453373277 Functional Loss DEL dbSNP153 33..34 33 - - - 78337 RMVar_ID_78337 Human_SNP_ID_471746488 m1A Human chr11 - 71786802 71786800 71786802 AAGAGACTGGGAGGCGGGTCGGGGCTGGGCTCAGGGGCGGAGAGGGAGCTGGGCTTGGGGCTGGG AAGAGACTGGGAGGCGGGTCGGGGCTGGGCTC__GGGCGGAGAGGGAGCTGGGCTTGGGGCTGGG CCT C AP003498.1 Ensembl:ENSG00000248671 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71786754..71786830 26863196 MeRIP-seq:(Medium) rs1379265462 Functional Loss DEL dbSNP153 33..34 33 - - - 78338 RMVar_ID_78338 Human_SNP_ID_471746905 m1A Human chr11 - 71787582 71787582 71787582 CAGGGCGCGCGCTGCCAGGAAGCGGCGCTTGAAACTCTGCAGCAAGAGTTCGCTCCCCGCGTTCT CAGGGCGCGCGCTGCCAGGAAGCGGCGCTTGATACTCTGCAGCAAGAGTTCGCTCCCCGCGTTCT T A AP003498.1 Ensembl:ENSG00000248671 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:71787540..71787691 26863196 MeRIP-seq:(Medium) rs1434264939 Functional Loss SNV dbSNP153 33..33 33 - - - 78339 RMVar_ID_78339 Human_SNP_ID_471750250 m1A Human chr11 + 71796912 71796912 71796912 GCAGCAGCCTCTGCCTGCACACAGAGACACGGACAAGCCAGTGCCTGTCCACGTGGGGCAGCCCG GCAGCAGCCTCTGCCTGCACACAGAGACACGGGCAAGCCAGTGCCTGTCCACGTGGGGCAGCCCG A G FAM86C1 Ensembl:ENSG00000158483 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71796884..71797014 26863196 MeRIP-seq:(Medium) rs1235068389 Functional Loss SNV dbSNP153 33..33 33 - - - 78340 RMVar_ID_78340 Human_SNP_ID_471751613 m1A Human chr11 + 71800418 71800418 71800418 TGCAGAGGTCACAGGGAAGTCACAGAACAGTAATACGCTAGCAGGGGCATGGGGCGTGAAGAACA TGCAGAGGTCACAGGGAAGTCACAGAACAGTAGTACGCTAGCAGGGGCATGGGGCGTGAAGAACA A G FAM86C1 Ensembl:ENSG00000158483 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71800367..71800455 26863196 MeRIP-seq:(Medium) rs1228428515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1741138 78341 RMVar_ID_78341 Human_SNP_ID_471796311 m1A Human chr11 - 71957186 71957186 71957186 AGACACCACCAGAAAAATCCGTTACTGTCTTAAAACTGTCCCTGCCAATATAAGGTGCTCACACA AGACACCACCAGAAAAATCCGTTACTGTCTTACAACTGTCCCTGCCAATATAAGGTGCTCACACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71957184..71957302 26863196 MeRIP-seq:(Medium) rs750475798 Functional Loss SNV dbSNP153 33..33 33 - - - 78342 RMVar_ID_78342 Human_SNP_ID_471797146 m1A Human chr11 - 71960692 71960692 71960692 TCAAGTCAGGGATGCTGTAGTGATAAAGGGACAGTGCTTTCCAGGGATATCCCACCAGTACATAG TCAAGTCAGGGATGCTGTAGTGATAAAGGGACGGTGCTTTCCAGGGATATCCCACCAGTACATAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:71960688..71960830 26863196 MeRIP-seq:(Medium) rs546837732 Functional Loss SNV dbSNP153 33..33 33 - - - 78343 RMVar_ID_78343 Human_SNP_ID_471806420 m1A Human chr11 - 71999136 71999136 71999136 TGGCCTTTCCCAGGCTACCCACTCCCCCAGCCACCAGCCCCAAGGTCGGCTACATCTCCCAGCAC TGGCCTTTCCCAGGCTACCCACTCCCCCAGCCGCCAGCCCCAAGGTCGGCTACATCTCCCAGCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:71999086..71999187 32194978 MeRIP-seq:(Medium) rs952699583 Functional Loss SNV dbSNP153 33..33 33 - - - 78344 RMVar_ID_78344 Human_SNP_ID_471806433 m1A Human chr11 - 71999157 71999157 71999157 CATACCAGTCCGTCCACATCCTGGCCTTTCCCAGGCTACCCACTCCCCCAGCCACCAGCCCCAAG CATACCAGTCCGTCCACATCCTGGCCTTTCCCCGGCTACCCACTCCCCCAGCCACCAGCCCCAAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:71999108..71999285 26863196 MeRIP-seq:(Medium) rs1260674330 Functional Loss SNV dbSNP153 33..33 33 - - - 78345 RMVar_ID_78345 Human_SNP_ID_471807903 m1A Human chr11 - 72003482 72003480 72003482 AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGACCTCACCTGGTCCTCCGCCTACTGTCCCTCTC AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGCCGTCACCTGGTCCTCCGCCTACTGTCCCTCTC GGT CGG NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs386754843 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_871459,Human_RBP_ID_9276008,Human_RBP_ID_17649229,Human_RBP_ID_26406744 Human_Splice_Rec_1272206,Human_Splice_Rec_1272230,Human_Splice_Rec_1272278,Human_Splice_Rec_1272330,Human_Splice_Rec_1272382,Human_Splice_Rec_1272428,Human_Splice_Rec_1272476,Human_Splice_Rec_1272522 Human_miRNA_ID_188716,Human_miRNA_ID_2007100 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494 78346 RMVar_ID_78346 Human_SNP_ID_471807904 m1A Human chr11 - 72003482 72003480 72003482 AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGACCTCACCTGGTCCTCCGCCTACTGTCCCTCTC AGTGAGTGGCCCCACCTGTGTCCCCGATGCTG__CTCACCTGGTCCTCCGCCTACTGTCCCTCTC GGT G NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1565179002 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_871459,Human_RBP_ID_9276008,Human_RBP_ID_17649229,Human_RBP_ID_26406744 Human_Splice_Rec_1272206,Human_Splice_Rec_1272230,Human_Splice_Rec_1272278,Human_Splice_Rec_1272330,Human_Splice_Rec_1272382,Human_Splice_Rec_1272428,Human_Splice_Rec_1272476,Human_Splice_Rec_1272522 Human_miRNA_ID_188716,Human_miRNA_ID_2007100 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494 78347 RMVar_ID_78347 Human_SNP_ID_471807909 m1A Human chr11 - 72003482 72003482 72003482 AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGACCTCACCTGGTCCTCCGCCTACTGTCCCTCTC AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGCCCTCACCTGGTCCTCCGCCTACTGTCCCTCTC T G NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs949323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871459,Human_RBP_ID_9276008,Human_RBP_ID_17649229,Human_RBP_ID_26406744 Human_Splice_Rec_1272206,Human_Splice_Rec_1272230,Human_Splice_Rec_1272278,Human_Splice_Rec_1272330,Human_Splice_Rec_1272382,Human_Splice_Rec_1272428,Human_Splice_Rec_1272476,Human_Splice_Rec_1272522 Human_miRNA_ID_188716,Human_miRNA_ID_2007100 Clinvar_Rec_361,Clinvar_Rec_362,Clinvar_Rec_3376,Clinvar_Rec_3377 GWAS_ID_9354,GWAS_ID_9355,GWAS_ID_9356,GWAS_ID_9357,GWAS_ID_9358,GWAS_ID_9359,GWAS_ID_9360,GWAS_ID_9361,GWAS_ID_9362,GWAS_ID_9363 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494 78348 RMVar_ID_78348 Human_SNP_ID_471807922 m1A Human chr11 + 72003512 72003512 72003512 GGTCAGCATCGGGGACACAGGTGGGGCCACTCACTGGTACTGGCCCTTTAGTGCTTTGCCTGAAA GGTCAGCATCGGGGACACAGGTGGGGCCACTCCCTGGTACTGGCCCTTTAGTGCTTTGCCTGAAA A C IL18BP Ensembl:ENSG00000137496 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72003462..72003961 32194978 MeRIP-seq:(Medium) rs771255287 Functional Loss SNV dbSNP153 33..33 33 - - - 78349 RMVar_ID_78349 Human_SNP_ID_471809281 m1A Human chr11 - 72007355 72007355 72007355 AGCCTCACCTATCTCCCAGCGCCTGCCCCCCAAGGTAGAATCCCTGGAGAGTCTCTACTTCACTC AGCCTCACCTATCTCCCAGCGCCTGCCCCCCAGGGTAGAATCCCTGGAGAGTCTCTACTTCACTC T C NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72007312..72007380 26863196 MeRIP-seq:(Medium) rs746618271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773835,Human_RBP_ID_9364054 Human_Splice_Rec_1272218,Human_Splice_Rec_1272266,Human_Splice_Rec_1272318,Human_Splice_Rec_1272370,Human_Splice_Rec_1272416,Human_Splice_Rec_1272464,Human_Splice_Rec_1272510,Human_Splice_Rec_1272524 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78350 RMVar_ID_78350 Human_SNP_ID_471809310 m1A Human chr11 - 72007418 72007418 72007418 GTTTCCTTTCCATAGCAAGCTGCCTCGTACCCAGCCAGACGGCACCAGCGTCCCTGGAGAACCAG GTTTCCTTTCCATAGCAAGCTGCCTCGTACCCCGCCAGACGGCACCAGCGTCCCTGGAGAACCAG T G NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72007311..72007455 26863196 MeRIP-seq:(Medium) rs776975644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871471,Human_RBP_ID_9362697,Human_RBP_ID_17800653,Human_RBP_ID_19050199,Human_RBP_ID_22537742,Human_RBP_ID_22641824,Human_RBP_ID_24901310,Human_RBP_ID_26318953 Human_Splice_Rec_1272218,Human_Splice_Rec_1272266,Human_Splice_Rec_1272318,Human_Splice_Rec_1272370,Human_Splice_Rec_1272416,Human_Splice_Rec_1272464,Human_Splice_Rec_1272510,Human_Splice_Rec_1272524 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78351 RMVar_ID_78351 Human_SNP_ID_471809317 m1A Human chr11 - 72007437 72007437 72007437 AAGGACTGTACCTCAGCAGGTTTCCTTTCCATAGCAAGCTGCCTCGTACCCAGCCAGACGGCACC AAGGACTGTACCTCAGCAGGTTTCCTTTCCATGGCAAGCTGCCTCGTACCCAGCCAGACGGCACC T C NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72007387..72007898 26863196 MeRIP-seq:(Medium) rs1248441855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22537742,Human_RBP_ID_22641824,Human_RBP_ID_26318953 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78352 RMVar_ID_78352 Human_SNP_ID_471809366 m1A Human chr11 - 72007601 72007601 72007601 TTAGGAGAAGCCAGGGGAGTGGACTGAAAGGAAGGCCCAGGTCAAGTGCTTTCCTTGGTACCTCT TTAGGAGAAGCCAGGGGAGTGGACTGAAAGGAGGGCCCAGGTCAAGTGCTTTCCTTGGTACCTCT T C NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72007594..72007835 26863196 MeRIP-seq:(Medium) rs1298223330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9343800,Human_RBP_ID_23267812,Human_RBP_ID_26318954 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78353 RMVar_ID_78353 Human_SNP_ID_471809388 m1A Human chr11 - 72007691 72007691 72007691 TTAGATTGGGACGTGTTTGCTGTGAAGCAGCCATGGGCATCTGGTGGGGATGGGACATCTGGGTC TTAGATTGGGACGTGTTTGCTGTGAAGCAGCCGTGGGCATCTGGTGGGGATGGGACATCTGGGTC T C NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72007686..72007887 32194978 MeRIP-seq:(Medium) rs1049300908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23267640 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78354 RMVar_ID_78354 Human_SNP_ID_471809729 m1A Human chr11 - 72008740 72008740 72008740 AGCCCCAGGCTAAGCCCCAGCTGGACTTGAGTATTGACAGCCTGGATCTGAGCTGCGAGGAGGGG AGCCCCAGGCTAAGCCCCAGCTGGACTTGAGTGTTGACAGCCTGGATCTGAGCTGCGAGGAGGGG T C NUMA1 Ensembl:ENSG00000137497 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72008677..72008794 26863196 MeRIP-seq:(Medium) rs1386457278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4194452,Human_RBP_ID_8358092,Human_RBP_ID_8771615,Human_RBP_ID_22491748,Human_RBP_ID_26317847 Human_Splice_Rec_1272215,Human_Splice_Rec_1272265,Human_Splice_Rec_1272317,Human_Splice_Rec_1272369,Human_Splice_Rec_1272415,Human_Splice_Rec_1272463,Human_Splice_Rec_1272509 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 78355 RMVar_ID_78355 Human_SNP_ID_471811009 m1A Human chr11 - 72012965 72012965 72012965 CCGGGAGCTGGAGGTGATGACTGCCAAGTATGAGGGTGCCAAGGTCAAGGTCCTGGAGGAGAGGC CCGGGAGCTGGAGGTGATGACTGCCAAGTATGCGGGTGCCAAGGTCAAGGTCCTGGAGGAGAGGC T G NUMA1 Ensembl:ENSG00000137497 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72012876..72013606 26863196 MeRIP-seq:(Medium) rs759026973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30595,Human_RBP_ID_3941042,Human_RBP_ID_4177174,Human_RBP_ID_5111224,Human_RBP_ID_5520823,Human_RBP_ID_9362702,Human_RBP_ID_18188353,Human_RBP_ID_21965843,Human_RBP_ID_26317848 Human_Splice_Rec_1272207,Human_Splice_Rec_1272309,Human_Splice_Rec_1272359,Human_Splice_Rec_1272407,Human_Splice_Rec_1272501,Human_Splice_Rec_1272529,Human_Splice_Rec_1272543 Human_miRNA_ID_1986698,Human_miRNA_ID_2217975,Human_miRNA_ID_3123220 RMVar_hsa_circ_103869,RMVar_hsa_circ_151494,RMVar_hsa_circ_113356,RMVar_hsa_circ_151495,RMVar_hsa_circ_358213 78356 RMVar_ID_78356 Human_SNP_ID_471811440 m1A Human chr11 - 72014019 72014019 72014019 AGGCTGAGCGGGCCTCCCGGGCTGAGCGGGACAGTGCTCTGGAGACTCTGCAGGGCCAGTTAGAG AGGCTGAGCGGGCCTCCCGGGCTGAGCGGGACGGTGCTCTGGAGACTCTGCAGGGCCAGTTAGAG T C NUMA1 Ensembl:ENSG00000137497 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:72014001..72014025 26863196 MeRIP-seq:(Medium) rs1565208681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30602,Human_RBP_ID_1782361,Human_RBP_ID_4177205,Human_RBP_ID_8771626 RMVar_hsa_circ_103869,RMVar_hsa_circ_151494,RMVar_hsa_circ_113356,RMVar_hsa_circ_151495,RMVar_hsa_circ_358213 78357 RMVar_ID_78357 Human_SNP_ID_471811806 m1A Human chr11 - 72015002 72015002 72015002 GGAGGCACAGTATGGCGCCATGTTCCAGGAACAGCTGATGACTTTGAAGGAGGAATGTGAGAAGG GGAGGCACAGTATGGCGCCATGTTCCAGGAACCGCTGATGACTTTGAAGGAGGAATGTGAGAAGG T G NUMA1 Ensembl:ENSG00000137497 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:72014951..72015025 26863196 MeRIP-seq:(Medium) rs780400469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30608,Human_RBP_ID_988298,Human_RBP_ID_4177236,Human_RBP_ID_6091617,Human_RBP_ID_8771635,Human_RBP_ID_17804701,Human_RBP_ID_18612474,Human_RBP_ID_26318970,Human_RBP_ID_27571899 RMVar_hsa_circ_103869,RMVar_hsa_circ_151494,RMVar_hsa_circ_113356,RMVar_hsa_circ_151495,RMVar_hsa_circ_358213 78358 RMVar_ID_78358 Human_SNP_ID_471812097 m1A Human chr11 - 72015797 72015797 72015797 TAGCCTGAAGCAGAAGGAGCAGCAGTTGAAGGAGGTAGCGGAGAAGCAGGAGGCAACTAGGCAGG TAGCCTGAAGCAGAAGGAGCAGCAGTTGAAGGCGGTAGCGGAGAAGCAGGAGGCAACTAGGCAGG T G NUMA1 Ensembl:ENSG00000137497 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72015651..72015952 26863196 MeRIP-seq:(Medium) rs1427034399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30613,Human_RBP_ID_26318977 RMVar_hsa_circ_103869,RMVar_hsa_circ_151494,RMVar_hsa_circ_113356,RMVar_hsa_circ_151495,RMVar_hsa_circ_358213 78359 RMVar_ID_78359 Human_SNP_ID_471818310 m1A Human chr11 + 72041032 72041031 72041032 CATTAGCATTTAAATCTTGAAAGGAGAGGAGGAAGGGGGGGCCAGTGGAAAGTAACCCCACACAC CATTAGCATTTAAATCTTGAAAGGAGAGGAGG_AGGGGGGGCCAGTGGAAAGTAACCCCACACAC GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72041020..72041085 26863196 MeRIP-seq:(Medium) rs1389837974 Functional Loss DEL dbSNP153 33..33 33 - - - 78360 RMVar_ID_78360 Human_SNP_ID_471818311 m1A Human chr11 + 72041032 72041032 72041032 CATTAGCATTTAAATCTTGAAAGGAGAGGAGGAAGGGGGGGCCAGTGGAAAGTAACCCCACACAC CATTAGCATTTAAATCTTGAAAGGAGAGGAGGGAGGGGGGGCCAGTGGAAAGTAACCCCACACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72041020..72041085 26863196 MeRIP-seq:(Medium) rs577779147 Functional Loss SNV dbSNP153 33..33 33 - - - 78361 RMVar_ID_78361 Human_SNP_ID_471831671 m1A Human chr11 - 72097882 72097882 72097882 GTCTCCAGGATAGCTGCTTATGCCTACAGTGCACTTTCTCAGATCCGTGTGGACGCAAAAGAGGA GTCTCCAGGATAGCTGCTTATGCCTACAGTGCGCTTTCTCAGATCCGTGTGGACGCAAAAGAGGA T C LAMTOR1 Ensembl:ENSG00000149357 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72097753..72097929 26863196 MeRIP-seq:(Medium) rs565240390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403044,Human_RBP_ID_1460144,Human_RBP_ID_1782381,Human_RBP_ID_8358147,Human_RBP_ID_11703640,Human_RBP_ID_23519653,Human_RBP_ID_24462261 Human_Splice_Rec_1273136,Human_Splice_Rec_1273144,Human_Splice_Rec_1273158,Human_Splice_Rec_1273166 Human_miRNA_ID_54073,Human_miRNA_ID_61621,Human_miRNA_ID_384333,Human_miRNA_ID_560885,Human_miRNA_ID_568340,Human_miRNA_ID_1565946,Human_miRNA_ID_1571596,Human_miRNA_ID_1578779,Human_miRNA_ID_1586358,Human_miRNA_ID_1684321,Human_miRNA_ID_1942670,Human_miRNA_ID_1945716,Human_miRNA_ID_2116861,Human_miRNA_ID_2200438,Human_miRNA_ID_2203502,Human_miRNA_ID_2403958,Human_miRNA_ID_2805978,Human_miRNA_ID_2809121,Human_miRNA_ID_2812264,Human_miRNA_ID_2815964,Human_miRNA_ID_2863227,Human_miRNA_ID_3112956 RMVar_hsa_circ_151504,RMVar_hsa_circ_95369,RMVar_hsa_circ_99428,RMVar_hsa_circ_112115,RMVar_hsa_circ_97211,RMVar_hsa_circ_151506,RMVar_hsa_circ_89733,RMVar_hsa_circ_151505,RMVar_hsa_circ_151502,RMVar_hsa_circ_151503 78362 RMVar_ID_78362 Human_SNP_ID_471831676 m1A Human chr11 + 72097913 72097913 72097913 GTGCACTGTAGGCATAAGCAGCTATCCTGGAGACCTGAGACAGAGAGGGGCCGGGGAGGAGAGGA GTGCACTGTAGGCATAAGCAGCTATCCTGGAGGCCTGAGACAGAGAGGGGCCGGGGAGGAGAGGA A G LRTOMT,AP000812.5 Ensembl:ENSG00000184154,Ensembl:ENSG00000284922 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72097542..72097939 32194978 MeRIP-seq:(Medium) rs184909354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_112075 78363 RMVar_ID_78363 Human_SNP_ID_471833041 m1A Human chr11 + 72103146 72103146 72103146 GTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTAGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCC GTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTGGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCC A G LRTOMT,AP000812.5 Ensembl:ENSG00000184154,Ensembl:ENSG00000284922 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:72103144..72103300 26863410 MeRIP-seq:(Medium) rs1456541977 Functional Loss SNV dbSNP153 33..33 33 - - - 78364 RMVar_ID_78364 Human_SNP_ID_471833042 m1A Human chr11 + 72103146 72103146 72103146 GTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTAGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCC GTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTTGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCC A T LRTOMT,AP000812.5 Ensembl:ENSG00000184154,Ensembl:ENSG00000284922 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:72103144..72103300 26863410 MeRIP-seq:(Medium) rs1456541977 Functional Loss SNV dbSNP153 33..33 33 - - - 78365 RMVar_ID_78365 Human_SNP_ID_471833078 m1A Human chr11 + 72103223 72103223 72103223 AGTCCTCGTTCTCGCTGCTGTAGCAGCACCCCATGGCCGGGGTCGGGCCGGGCGCTCAGGCCGCG AGTCCTCGTTCTCGCTGCTGTAGCAGCACCCCCTGGCCGGGGTCGGGCCGGGCGCTCAGGCCGCG A C LRTOMT,AP000812.5 Ensembl:ENSG00000184154,Ensembl:ENSG00000284922 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72099253..72103325 26863196 MeRIP-seq:(Medium) rs1178700185 Functional Loss SNV dbSNP153 33..33 33 - - - 78366 RMVar_ID_78366 Human_SNP_ID_471834980 m1A Human chr11 - 72110164 72110164 72110164 TGAAGATGATGAGGATAGTGAAGAGGACTCAGAGGATGATGAGGATATGCAGGACATGGACGAGA TGAAGATGATGAGGATAGTGAAGAGGACTCAGGGGATGATGAGGATATGCAGGACATGGACGAGA T C ANAPC15 Ensembl:ENSG00000110200 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:72109801..72110250 26863196 MeRIP-seq:(Medium) rs765381065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8358156,Human_RBP_ID_11703708,Human_RBP_ID_17805302,Human_RBP_ID_23519658,Human_RBP_ID_26318981,Human_RBP_ID_27415869,Human_RBP_ID_27804872 Human_Splice_Rec_1273178,Human_Splice_Rec_1273179,Human_Splice_Rec_1273186,Human_Splice_Rec_1273187,Human_Splice_Rec_1273194,Human_Splice_Rec_1273195,Human_Splice_Rec_1273206,Human_Splice_Rec_1273207,Human_Splice_Rec_1273209,Human_Splice_Rec_1273218,Human_Splice_Rec_1273219,Human_Splice_Rec_1273228,Human_Splice_Rec_1273229,Human_Splice_Rec_1273238,Human_Splice_Rec_1273239,Human_Splice_Rec_1273248,Human_Splice_Rec_1273249,Human_Splice_Rec_1273256,Human_Splice_Rec_1273257,Human_Splice_Rec_1273266,Human_Splice_Rec_1273267,Human_Splice_Rec_1273276,Human_Splice_Rec_1273277,Human_Splice_Rec_1273286,Human_Splice_Rec_1273287,Human_Splice_Rec_1273296,Human_Splice_Rec_1273302,Human_Splice_Rec_1273310 RMVar_hsa_circ_27936,RMVar_hsa_circ_104831,RMVar_hsa_circ_151508 78367 RMVar_ID_78367 Human_SNP_ID_471835325 m1A Human chr11 + 72111290 72111290 72111290 AGGGGAACAAAGTGGACATGGCTCCTAGACTGAGGGAAAGGGTCAAGTGAATGTGTTTTGCTTTG AGGGGAACAAAGTGGACATGGCTCCTAGACTGGGGGAAAGGGTCAAGTGAATGTGTTTTGCTTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72111287..72111383 26863196 MeRIP-seq:(Medium) rs1316955498 Functional Loss SNV dbSNP153 33..33 33 - - - 78368 RMVar_ID_78368 Human_SNP_ID_471835529 m1A Human chr11 - 72112137 72112137 72112137 AGGGAAGGGCAGCGGCTGGCCCTGGGTCGGTCAGATAAATTAAGACAAAAGCAGGACCAGGCATC AGGGAAGGGCAGCGGCTGGCCCTGGGTCGGTCGGATAAATTAAGACAAAAGCAGGACCAGGCATC T C ANAPC15 Ensembl:ENSG00000110200 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72112134..72112234 26863196 MeRIP-seq:(Medium) rs1268906071 Functional Loss SNV dbSNP153 33..33 33 - - - 78369 RMVar_ID_78369 Human_SNP_ID_471835737 m1A Human chr11 - 72112700 72112700 72112700 TGAGTCCCGGATTCTGGTGGGTTCTTCCGCTCAGGCTGGGTGAAGCGCTTCCGGGTCGCCGCCGG TGAGTCCCGGATTCTGGTGGGTTCTTCCGCTCGGGCTGGGTGAAGCGCTTCCGGGTCGCCGCCGG T C ANAPC15 Ensembl:ENSG00000110200 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72112432..72112730 32194978 MeRIP-seq:(Medium) rs1421024838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4177430 Human_Splice_Rec_1273175,Human_Splice_Rec_1273199,Human_Splice_Rec_1273211,Human_Splice_Rec_1273221,Human_Splice_Rec_1273241,Human_Splice_Rec_1273251,Human_Splice_Rec_1273259 78370 RMVar_ID_78370 Human_SNP_ID_471835750 m1A Human chr11 + 72112721 72112721 72112721 TTCACCCAGCCTGAGCGGAAGAACCCACCAGAATCCGGGACTCACCAAACGCATGCGTCCTTCGT TTCACCCAGCCTGAGCGGAAGAACCCACCAGACTCCGGGACTCACCAAACGCATGCGTCCTTCGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72112605..72112750 26863196 MeRIP-seq:(Medium) rs1398006457 Functional Loss SNV dbSNP153 33..33 33 - - - 78371 RMVar_ID_78371 Human_SNP_ID_471835751 m1A Human chr11 - 72112722 72112722 72112722 GACGAAGGACGCATGCGTTTGGTGAGTCCCGGATTCTGGTGGGTTCTTCCGCTCAGGCTGGGTGA GACGAAGGACGCATGCGTTTGGTGAGTCCCGGCTTCTGGTGGGTTCTTCCGCTCAGGCTGGGTGA T G ANAPC15 Ensembl:ENSG00000110200 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:72112584..72112725;chr11:72112432..72112730 26863196 MeRIP-seq:(Medium) rs1354790720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185253 Human_Splice_Rec_1273175,Human_Splice_Rec_1273199,Human_Splice_Rec_1273211,Human_Splice_Rec_1273221,Human_Splice_Rec_1273241,Human_Splice_Rec_1273251,Human_Splice_Rec_1273259 78372 RMVar_ID_78372 Human_SNP_ID_471864389 m1A Human chr11 + 72223918 72223918 72223918 GGATGGCCATCTTAAGTGGCCGCCTGGAGCCCAGGGCCGCTGTCCGGGGAAGGGGGCGCCGGAGC GGATGGCCATCTTAAGTGGCCGCCTGGAGCCCTGGGCCGCTGTCCGGGGAAGGGGGCGCCGGAGC A T INPPL1 Ensembl:ENSG00000165458 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:72223893..72224067 26863196 MeRIP-seq:(Medium) rs1035169187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8774469,Human_RBP_ID_9276027,Human_RBP_ID_18416623 Human_Splice_Rec_1273451 78373 RMVar_ID_78373 Human_SNP_ID_471864404 m1A Human chr11 + 72223959 72223959 72223959 GTCCGGGGAAGGGGGCGCCGGAGCAGCCCGGGAGGTGGGGGTCTGCGTGCGGCGGCCGGGATCCC GTCCGGGGAAGGGGGCGCCGGAGCAGCCCGGGGGGTGGGGGTCTGCGTGCGGCGGCCGGGATCCC A G INPPL1 Ensembl:ENSG00000165458 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:72223876..72224122;chr11:72223876..72224182;chr11:72223876..72224207 26863196 MeRIP-seq:(Medium) rs1273726517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3384459,Human_RBP_ID_8774469,Human_RBP_ID_9322285,Human_RBP_ID_9414642,Human_RBP_ID_18416623,Human_RBP_ID_21966679,Human_RBP_ID_22569777 Human_Splice_Rec_1273451 78374 RMVar_ID_78374 Human_SNP_ID_471864872 m1A Human chr11 - 72225376 72225376 72225376 TGGGCCACAGAACCCCATATTCTCTACCCTCAAGGCTCCTGAAAGTGCCCCCAGACACACAGCAG TGGGCCACAGAACCCCATATTCTCTACCCTCAGGGCTCCTGAAAGTGCCCCCAGACACACAGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72225364..72225626 26863196 MeRIP-seq:(Medium) rs1463701793 Functional Loss SNV dbSNP153 33..33 33 - - - 78375 RMVar_ID_78375 Human_SNP_ID_471865590 m1A Human chr11 - 72228180 72228180 72228180 ACGTGTGCACATGCTTCTGATACCTGATGCCAAGGCAGGGCCAGAATCTGTCACCCCCAGGCTGG ACGTGTGCACATGCTTCTGATACCTGATGCCAGGGCAGGGCCAGAATCTGTCACCCCCAGGCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72228176..72228275 26863196 MeRIP-seq:(Medium) rs151303117 Functional Loss SNV dbSNP153 33..33 33 - - - 78376 RMVar_ID_78376 Human_SNP_ID_471865591 m1A Human chr11 - 72228180 72228180 72228180 ACGTGTGCACATGCTTCTGATACCTGATGCCAAGGCAGGGCCAGAATCTGTCACCCCCAGGCTGG ACGTGTGCACATGCTTCTGATACCTGATGCCACGGCAGGGCCAGAATCTGTCACCCCCAGGCTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72228176..72228275 26863196 MeRIP-seq:(Medium) rs151303117 Functional Loss SNV dbSNP153 33..33 33 - - - 78377 RMVar_ID_78377 Human_SNP_ID_471865662 m1A Human chr11 - 72228361 72228361 72228361 GCTCACCCAGGGTCTGGAAGCGGCGCACAGGCACACCCTGCGAGGTCTGTGGGCCAGCAAGGGTG GCTCACCCAGGGTCTGGAAGCGGCGCACAGGCGCACCCTGCGAGGTCTGTGGGCCAGCAAGGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72228351..72228375 26863196 MeRIP-seq:(Medium) rs1191142962 Functional Loss SNV dbSNP153 33..33 33 - - - 78378 RMVar_ID_78378 Human_SNP_ID_471865789 m1A Human chr11 - 72228670 72228670 72228670 CCGTTTGGGCCTCCCACACTCAGTGGAGTAGGAGGCACGATGCAGCTGTAAAGTGACTTCCATGG CCGTTTGGGCCTCCCACACTCAGTGGAGTAGGGGGCACGATGCAGCTGTAAAGTGACTTCCATGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72228667..72228758 26863196 MeRIP-seq:(Medium) rs1320120099 Functional Loss SNV dbSNP153 33..33 33 - - - 78379 RMVar_ID_78379 Human_SNP_ID_471865794 m1A Human chr11 + 72228691 72228691 72228691 TGCATCGTGCCTCCTACTCCACTGAGTGTGGGAGGCCCAAACGGCTGCCCACTGACCCCTGCCCA TGCATCGTGCCTCCTACTCCACTGAGTGTGGGTGGCCCAAACGGCTGCCCACTGACCCCTGCCCA A T INPPL1 Ensembl:ENSG00000165458 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72228687..72228850 32194978 MeRIP-seq:(Medium) rs767268219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126746,Human_RBP_ID_22537748 RMVar_hsa_circ_19267,RMVar_hsa_circ_13696,RMVar_hsa_circ_266009,RMVar_hsa_circ_11656,RMVar_hsa_circ_127173,RMVar_hsa_circ_151510 78380 RMVar_ID_78380 Human_SNP_ID_471868108 m1A Human chr11 + 72235393 72235393 72235393 TCCCACCGTGGCGAGGAGACAGGCAATATCAGAGGCTCCATGAAGGTGCGGGTGCCCACGGAGCG TCCCACCGTGGCGAGGAGACAGGCAATATCAGGGGCTCCATGAAGGTGCGGGTGCCCACGGAGCG A G INPPL1 Ensembl:ENSG00000165458 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72235342..72235466 26863196 MeRIP-seq:(Medium) rs1405937356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520853,Human_RBP_ID_5550211 Human_Splice_Rec_1273496,Human_Splice_Rec_1273497,Human_Splice_Rec_1273552,Human_Splice_Rec_1273553,Human_Splice_Rec_1273604,Human_Splice_Rec_1273605,Human_Splice_Rec_1273654,Human_Splice_Rec_1273666,Human_Splice_Rec_1273667 RMVar_hsa_circ_82190,RMVar_hsa_circ_151524,RMVar_hsa_circ_99328,RMVar_hsa_circ_151525 78381 RMVar_ID_78381 Human_SNP_ID_471868216 m1A Human chr11 + 72235747 72235747 72235747 CAAAGCCCCCTCTGTGTCCCGAGGGAGCCAGGAGCCCAGGTGAGCTAGGGCTGTGTTGAATGTCA CAAAGCCCCCTCTGTGTCCCGAGGGAGCCAGGCGCCCAGGTGAGCTAGGGCTGTGTTGAATGTCA A C INPPL1 Ensembl:ENSG00000165458 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72235649..72235803 26863196 MeRIP-seq:(Medium) rs769484758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18972543,Human_RBP_ID_22571498 Human_Splice_Rec_1273498,Human_Splice_Rec_1273499,Human_Splice_Rec_1273554,Human_Splice_Rec_1273555,Human_Splice_Rec_1273606,Human_Splice_Rec_1273607,Human_Splice_Rec_1273668,Human_Splice_Rec_1273669 RMVar_hsa_circ_82190,RMVar_hsa_circ_151525 78382 RMVar_ID_78382 Human_SNP_ID_471868217 m1A Human chr11 + 72235747 72235747 72235747 CAAAGCCCCCTCTGTGTCCCGAGGGAGCCAGGAGCCCAGGTGAGCTAGGGCTGTGTTGAATGTCA CAAAGCCCCCTCTGTGTCCCGAGGGAGCCAGGGGCCCAGGTGAGCTAGGGCTGTGTTGAATGTCA A G INPPL1 Ensembl:ENSG00000165458 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72235649..72235803 26863196 MeRIP-seq:(Medium) rs769484758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18972543,Human_RBP_ID_22571498 Human_Splice_Rec_1273498,Human_Splice_Rec_1273499,Human_Splice_Rec_1273554,Human_Splice_Rec_1273555,Human_Splice_Rec_1273606,Human_Splice_Rec_1273607,Human_Splice_Rec_1273668,Human_Splice_Rec_1273669 RMVar_hsa_circ_82190,RMVar_hsa_circ_151525 78383 RMVar_ID_78383 Human_SNP_ID_471868626 m1A Human chr11 + 72237225 72237225 72237225 CCCTGCCTACTACGTCCTTGAAGGGGTCCCGCACCAGCTGCTGCCCCCGGAGCCACCCTCGCCTG CCCTGCCTACTACGTCCTTGAAGGGGTCCCGCCCCAGCTGCTGCCCCCGGAGCCACCCTCGCCTG A C INPPL1 Ensembl:ENSG00000165458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72237176..72237298 26863196 MeRIP-seq:(Medium) rs1249936544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226833,Human_RBP_ID_3939698,Human_RBP_ID_5110952 Human_miRNA_ID_2051776 RMVar_hsa_circ_95334,RMVar_hsa_circ_151526 78384 RMVar_ID_78384 Human_SNP_ID_471868689 m1A Human chr11 - 72237403 72237403 72237403 AAGATGGCTGAGTCCGGCAGTGGTGGAGGTGGAAAGTCTGGAGGGGGCAGTGTGCCTCCAGACTC AAGATGGCTGAGTCCGGCAGTGGTGGAGGTGGGAAGTCTGGAGGGGGCAGTGTGCCTCCAGACTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:72237310..72237496 26863196 MeRIP-seq:(Medium) rs754900169 Functional Loss SNV dbSNP153 33..33 33 - - - 78385 RMVar_ID_78385 Human_SNP_ID_471890285 m1A Human chr11 + 72329716 72329716 72329716 CTCCTCCCTTCCCTGAGACTTACCTTGGCTTCAGAAGTCCTCAGAAGCTTCATCACTTCCCCTTC CTCCTCCCTTCCCTGAGACTTACCTTGGCTTCGGAAGTCCTCAGAAGCTTCATCACTTCCCCTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72329701..72329725 32194978 MeRIP-seq:(Medium) rs1441561783 Functional Loss SNV dbSNP153 33..33 33 - - - 78386 RMVar_ID_78386 Human_SNP_ID_471901013 m1A Human chr11 + 72380351 72380351 72380351 TAAACACTGCTGAAATCATCTCCAAGGTTTGGATCAGCCCCAGCAGCAAGCAGGACCTGTACCAC TAAACACTGCTGAAATCATCTCCAAGGTTTGGCTCAGCCCCAGCAGCAAGCAGGACCTGTACCAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:72380326..72380350 32194978 MeRIP-seq:(Medium) rs1297783130 Functional Loss SNV dbSNP153 33..33 33 - - - 78387 RMVar_ID_78387 Human_SNP_ID_471913400 m1A Human chr11 + 72434473 72434473 72434473 GTGCTTTTCTCCTCAACACCAGGGACCCCAGCATCTTGACAGCTGCTTCGATAACCCCGTGGTGC GTGCTTTTCTCCTCAACACCAGGGACCCCAGCGTCTTGACAGCTGCTTCGATAACCCCGTGGTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72434281..72434525 26863196 MeRIP-seq:(Medium) rs369149141 Functional Loss SNV dbSNP153 33..33 33 - - - 78388 RMVar_ID_78388 Human_SNP_ID_471913403 m1A Human chr11 + 72434481 72434481 72434481 CTCCTCAACACCAGGGACCCCAGCATCTTGACAGCTGCTTCGATAACCCCGTGGTGCCGGCCCCT CTCCTCAACACCAGGGACCCCAGCATCTTGACGGCTGCTTCGATAACCCCGTGGTGCCGGCCCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72434201..72434502 26863196 MeRIP-seq:(Medium) rs1284099328 Functional Loss SNV dbSNP153 33..33 33 - - - 78389 RMVar_ID_78389 Human_SNP_ID_471976678 m1A Human chr11 + 72686154 72686154 72686154 TACCCAGCCGGACCTCAGGCACTGCCCGGGACACGCGTGAGGGCTCTGAGGGCCACACCAGGCCG TACCCAGCCGGACCTCAGGCACTGCCCGGGACCCGCGTGAGGGCTCTGAGGGCCACACCAGGCCG A C ARAP1-AS1 Ensembl:ENSG00000256007 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr11:72686105..72686187;chr11:72686076..72687294 26863196,32194978 MeRIP-seq:(Medium) rs748005955 Functional Loss SNV dbSNP153 33..33 33 - - - 78390 RMVar_ID_78390 Human_SNP_ID_471979213 m1A Human chr11 - 72695839 72695839 72695839 CTCCAGTGTTCAGTGCTTCTCAGACACGAACCAGATGAACGTGCACAACCTGGCAATTGTGTTTG CTCCAGTGTTCAGTGCTTCTCAGACACGAACCGGATGAACGTGCACAACCTGGCAATTGTGTTTG T C ARAP1 Ensembl:ENSG00000186635 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72695790..72696673 32194978 MeRIP-seq:(Medium) rs1018327868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23519895 Human_Splice_Rec_1274706,Human_Splice_Rec_1274772,Human_Splice_Rec_1274808,Human_Splice_Rec_1274866,Human_Splice_Rec_1274924,Human_Splice_Rec_1274988,Human_Splice_Rec_1275056,Human_Splice_Rec_1275120,Human_Splice_Rec_1275180,Human_Splice_Rec_1275256 RMVar_hsa_circ_10915,RMVar_hsa_circ_62676,RMVar_hsa_circ_81133,RMVar_hsa_circ_151542,RMVar_hsa_circ_151544,RMVar_hsa_circ_126551,RMVar_hsa_circ_375087,RMVar_hsa_circ_151545,RMVar_hsa_circ_102375,RMVar_hsa_circ_151548,RMVar_hsa_circ_76563,RMVar_hsa_circ_111134,RMVar_hsa_circ_151547,RMVar_hsa_circ_78797,RMVar_hsa_circ_151549,RMVar_hsa_circ_151550 78391 RMVar_ID_78391 Human_SNP_ID_471984174 m1A Human chr11 + 72713238 72713238 72713238 CGGCCCCTCCTCTGGGACCTCATCGTAGTCAGAGTCATCTGGTGAGAGAGGGGTTGGGGGGCCTC CGGCCCCTCCTCTGGGACCTCATCGTAGTCAGTGTCATCTGGTGAGAGAGGGGTTGGGGGGCCTC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:72713105..72713250 26863196 MeRIP-seq:(Medium) rs993242829 Functional Loss SNV dbSNP153 33..33 33 - - - 78392 RMVar_ID_78392 Human_SNP_ID_471984543 m1A Human chr11 - 72714288 72714288 72714288 CTGCCCACTAAGGAGGAGGAGTCATTGCTGCCATCATTATCATCCCCTCCCCAGCCACAGTCTGA CTGCCCACTAAGGAGGAGGAGTCATTGCTGCCGTCATTATCATCCCCTCCCCAGCCACAGTCTGA T C ARAP1 Ensembl:ENSG00000186635 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72714239..72714375 26863196 MeRIP-seq:(Medium) rs935479494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3379637,Human_RBP_ID_5416309,Human_RBP_ID_5490690,Human_RBP_ID_17800800 Human_Splice_Rec_1274732,Human_Splice_Rec_1274830,Human_Splice_Rec_1274948,Human_Splice_Rec_1275016,Human_Splice_Rec_1275080,Human_Splice_Rec_1275142 Human_miRNA_ID_2367278 RMVar_hsa_circ_62676,RMVar_hsa_circ_81133,RMVar_hsa_circ_151542,RMVar_hsa_circ_28396,RMVar_hsa_circ_13102,RMVar_hsa_circ_36612,RMVar_hsa_circ_295428,RMVar_hsa_circ_151554,RMVar_hsa_circ_320814,RMVar_hsa_circ_151558,RMVar_hsa_circ_639,RMVar_hsa_circ_58932,RMVar_hsa_circ_35449,RMVar_hsa_circ_151560,RMVar_hsa_circ_127085 78393 RMVar_ID_78393 Human_SNP_ID_471985902 m1A Human chr11 - 72720228 72720228 72720228 ATGATTGAGGAAGCGGGCAGCTGGGACAGTTTACCCCTGTGGAATGGAGACATCAGGGTGGGACA ATGATTGAGGAAGCGGGCAGCTGGGACAGTTTTCCCCTGTGGAATGGAGACATCAGGGTGGGACA T A ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72720225..72720374 26863196 MeRIP-seq:(Medium) rs939955696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11704487 RMVar_hsa_circ_62676,RMVar_hsa_circ_13102,RMVar_hsa_circ_639 78394 RMVar_ID_78394 Human_SNP_ID_471987552 m1A Human chr11 + 72726878 72726878 72726878 GCACAGGTGGTGAGCGGAAGATGTGGCGCTTCATGGGCACAGGCCGTGGGGTGGGGCGGGGTGCA GCACAGGTGGTGAGCGGAAGATGTGGCGCTTCGTGGGCACAGGCCGTGGGGTGGGGCGGGGTGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:72726828..72727022 26863196 MeRIP-seq:(Medium) rs1353413456 Functional Loss SNV dbSNP153 33..33 33 - - - 78395 RMVar_ID_78395 Human_SNP_ID_471987566 m1A Human chr11 - 72726897 72726897 72726897 CCCATACCTCACCGGCCCCTGCACCCCGCCCCACCCCACGGCCTGTGCCCATGAAGCGCCACATC CCCATACCTCACCGGCCCCTGCACCCCGCCCCCCCCCACGGCCTGTGCCCATGAAGCGCCACATC T G ARAP1 Ensembl:ENSG00000186635 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:72726801..72726932 26863410 MeRIP-seq:(Medium) rs1375770101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_870822 RMVar_hsa_circ_62676,RMVar_hsa_circ_13102,RMVar_hsa_circ_639,RMVar_hsa_circ_355078 78396 RMVar_ID_78396 Human_SNP_ID_471987648 m1A Human chr11 + 72727062 72727062 72727062 CACCAGGCCATGCTGCTCAAAGAGCCCCGTGTACTGCTCCAGGTGCAATGCCCGCAGCCACTCGG CACCAGGCCATGCTGCTCAAAGAGCCCCGTGTTCTGCTCCAGGTGCAATGCCCGCAGCCACTCGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72726811..72727160 32194978 MeRIP-seq:(Medium) rs758207488 Functional Loss SNV dbSNP153 33..33 33 - - - 78397 RMVar_ID_78397 Human_SNP_ID_471993031 m1A Human chr11 - 72751330 72751329 72751330 CAATTTACAAGGATAAGGACCCTCCAAAGGCGAGGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA CAATTTACAAGGATAAGGACCCTCCAAAGGCG_GGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA CT C ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72751317..72751414 26863196 MeRIP-seq:(Medium) rs982000291 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_151561 78398 RMVar_ID_78398 Human_SNP_ID_471993032 m1A Human chr11 - 72751330 72751330 72751330 CAATTTACAAGGATAAGGACCCTCCAAAGGCGAGGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA CAATTTACAAGGATAAGGACCCTCCAAAGGCGGGGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA T C ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72751317..72751414 26863196 MeRIP-seq:(Medium) rs1785212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151561 78399 RMVar_ID_78399 Human_SNP_ID_471993392 m1A Human chr11 - 72752596 72752596 72752596 GGAAGACCCGCAAGCAGCTAGAGGGGCAGGAGAGAGACACAGACCGACGGGTCCGGCGGGCGGGC GGAAGACCCGCAAGCAGCTAGAGGGGCAGGAGGGAGACACAGACCGACGGGTCCGGCGGGCGGGC T C ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72752587..72752699 26863196 MeRIP-seq:(Medium) rs1436902119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151561 78400 RMVar_ID_78400 Human_SNP_ID_471993897 m1A Human chr11 + 72754828 72754828 72754828 GGTGCCACCAGGTGCCGGGTGGGGGAGGGGAGAAAGTGCAGGAGCGGCCGCCGCCCCAGGGCTCG GGTGCCACCAGGTGCCGGGTGGGGGAGGGGAGGAAGTGCAGGAGCGGCCGCCGCCCCAGGGCTCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72754777..72755012 26863196 MeRIP-seq:(Medium) rs767148675 Functional Loss SNV dbSNP153 33..33 33 - - - 78401 RMVar_ID_78401 Human_SNP_ID_471993951 m1A Human chr11 + 72754908 72754908 72754908 GTCCCTGAAGCGGTGCGGCGCTCAGGTGAGCGAGGTGTCGTCGTCGCTGCCCTCGCCGCCCGCGC GTCCCTGAAGCGGTGCGGCGCTCAGGTGAGCGTGGTGTCGTCGTCGCTGCCCTCGCCGCCCGCGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72754858..72754941 26863196 MeRIP-seq:(Medium) rs1397292055 Functional Loss SNV dbSNP153 33..33 33 - - - 78402 RMVar_ID_78402 Human_SNP_ID_472000084 m1A Human chr11 + 72781041 72781041 72781041 GCCTGCACCCAGACAGACACCCCAGCCCTGCTATAGGTCAGGTTCCAGCCCACCTCAGCCTCACA GCCTGCACCCAGACAGACACCCCAGCCCTGCTGTAGGTCAGGTTCCAGCCCACCTCAGCCTCACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:72780990..72781331 26863196 MeRIP-seq:(Medium) rs764962642 Functional Loss SNV dbSNP153 33..33 33 - - - 78403 RMVar_ID_78403 Human_SNP_ID_472000283 m1A Human chr11 + 72781648 72781648 72781648 GGGCGGGTGGCGGGGCAGGAGGGGCGCCCTCCAGGCCGGGCTGCTCACCTTTGCCCGCCGCTCCG GGGCGGGTGGCGGGGCAGGAGGGGCGCCCTCCGGGCCGGGCTGCTCACCTTTGCCCGCCGCTCCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:72781645..72781817 26863196 MeRIP-seq:(Medium) rs1237278710 Functional Loss SNV dbSNP153 33..33 33 - - - 78404 RMVar_ID_78404 Human_SNP_ID_472008249 m1A Human chr11 + 72814478 72814478 72814478 ATGGCGGGGCCGGGCGTCCCCGGTGCCCCCGCAGCGCGCTGGAAACGCCACATCGTGCGGCAGCT ATGGCGGGGCCGGGCGTCCCCGGTGCCCCCGCTGCGCGCTGGAAACGCCACATCGTGCGGCAGCT A T ATG16L2 Ensembl:ENSG00000168010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72814432..72814514 26863196 MeRIP-seq:(Medium) rs1181384979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416625 Human_Splice_Rec_1275457,Human_Splice_Rec_1275467,Human_Splice_Rec_1275501,Human_Splice_Rec_1275535,Human_Splice_Rec_1275565,Human_Splice_Rec_1275571,Human_Splice_Rec_1275577,Human_Splice_Rec_1275609 78405 RMVar_ID_78405 Human_SNP_ID_472008262 m1A Human chr11 - 72814510 72814510 72814510 AAAGCGCCTTTTGCGTACGGTCCCGAAGCCGCAGCTGCCGCACGATGTGGCGTTTCCAGCGCGCT AAAGCGCCTTTTGCGTACGGTCCCGAAGCCGCCGCTGCCGCACGATGTGGCGTTTCCAGCGCGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:72814464..72814598 26863196 MeRIP-seq:(Medium) rs772633981 Functional Loss SNV dbSNP153 33..33 33 - - - 78406 RMVar_ID_78406 Human_SNP_ID_472008882 m1A Human chr11 + 72816794 72816793 72816795 CAAGTTCTCAAAGAAGCTGCAGCCGGAGCCAAACAGTGTCACTCCCACCACCCACCAGGGCCCCT CAAGTTCTCAAAGAAGCTGCAGCCGGAGCCAA__AGTGTCACTCCCACCACCCACCAGGGCCCCT AAC A ATG16L2 Ensembl:ENSG00000168010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72816724..72816849 26863196 MeRIP-seq:(Medium) rs774810073 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18972592,Human_RBP_ID_27803816 Human_Splice_Rec_1275458,Human_Splice_Rec_1275459,Human_Splice_Rec_1275468,Human_Splice_Rec_1275469,Human_Splice_Rec_1275502,Human_Splice_Rec_1275503,Human_Splice_Rec_1275536,Human_Splice_Rec_1275537,Human_Splice_Rec_1275566,Human_Splice_Rec_1275567,Human_Splice_Rec_1275572,Human_Splice_Rec_1275573,Human_Splice_Rec_1275578,Human_Splice_Rec_1275579,Human_Splice_Rec_1275610,Human_Splice_Rec_1275611,Human_Splice_Rec_1275614,Human_Splice_Rec_1275615,Human_Splice_Rec_1275617 78407 RMVar_ID_78407 Human_SNP_ID_472010380 m1A Human chr11 + 72822169 72822169 72822169 GCAGCGGGCAGCCTACGAGGCGCTGCGCGCGCACGTCGGGCTCCGGGAGGCGGCACTGCGCAGGC GCAGCGGGCAGCCTACGAGGCGCTGCGCGCGCTCGTCGGGCTCCGGGAGGCGGCACTGCGCAGGC A T ATG16L2 Ensembl:ENSG00000168010 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72822034..72822202 26863196 MeRIP-seq:(Medium) rs775225390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364107,Human_RBP_ID_18974710,Human_RBP_ID_27803817 78408 RMVar_ID_78408 Human_SNP_ID_472012012 m1A Human chr11 - 72826825 72826825 72826825 GGGGAGGAGAGGTGGGGCTGGGGCTCGGGCTCACAATAGGCACGGCCGAGGTCCCACTCCTTCAC GGGGAGGAGAGGTGGGGCTGGGGCTCGGGCTCCCAATAGGCACGGCCGAGGTCCCACTCCTTCAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72826812..72826913 32194978 MeRIP-seq:(Medium) rs1204746131 Functional Loss SNV dbSNP153 33..33 33 - - - 78409 RMVar_ID_78409 Human_SNP_ID_472012128 m1A Human chr11 - 72827214 72827214 72827214 GATATGGTCCCCACACACCACGTCATTACAGTAGGAAAGGACATTGATGGTCCTGGAGCCTGGGG GATATGGTCCCCACACACCACGTCATTACAGTGGGAAAGGACATTGATGGTCCTGGAGCCTGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72827211..72828526 32194978 MeRIP-seq:(Medium) rs1343267547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1265740 78410 RMVar_ID_78410 Human_SNP_ID_472054887 m1A Human chr11 + 73004954 73004954 73004954 GGCAATGTCCACATGTTCCCACCACATTTGCCAAACTCCTTGTCTCTGCACCCATACATTATGCC GGCAATGTCCACATGTTCCCACCACATTTGCCGAACTCCTTGTCTCTGCACCCATACATTATGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73004938..73005032 26863196 MeRIP-seq:(Medium) rs1197122478 Functional Loss SNV dbSNP153 33..33 33 - - - 78411 RMVar_ID_78411 Human_SNP_ID_472087413 m1A Human chr11 + 73142003 73142003 73142003 GCGCGCGTGTGTGAAAGGAGCGCTTAAGAAGCAAGACTTGCCCCGGAGGGAGCAGGCCAGCGGGC GCGCGCGTGTGTGAAAGGAGCGCTTAAGAAGCGAGACTTGCCCCGGAGGGAGCAGGCCAGCGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73141963..73142204 26863196 MeRIP-seq:(Medium) rs1429687853 Functional Loss SNV dbSNP153 33..33 33 - - - 78412 RMVar_ID_78412 Human_SNP_ID_472124211 m1A Human chr11 + 73290285 73290269 73290286 AGAGAGAGGGGGAAAGAAAAGAAAGGAAGGAAAGAAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA AGAGAGAGGGGGAAAGA_________________AAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA AAAAGAAAGGAAGGAAAG A P2RY6 Ensembl:ENSG00000171631 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73290238..73290328 26863196 MeRIP-seq:(Medium) rs1428169247 Functional Loss DEL dbSNP153 18..34 33 - - - 78413 RMVar_ID_78413 Human_SNP_ID_472124225 m1A Human chr11 + 73290285 73290285 73290285 AGAGAGAGGGGGAAAGAAAAGAAAGGAAGGAAAGAAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA AGAGAGAGGGGGAAAGAAAAGAAAGGAAGGAAGGAAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA A G P2RY6 Ensembl:ENSG00000171631 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73290238..73290328 26863196 MeRIP-seq:(Medium) rs954525546 Functional Loss SNV dbSNP153 33..33 33 - - - 78414 RMVar_ID_78414 Human_SNP_ID_472124942 m1A Human chr11 - 73292313 73292313 73292313 ATGTGGCAATCCACTTACGTACAAACTTACTCAGCCGCCTTCTCCCCCCGCTTCCCTCTTCTTCT ATGTGGCAATCCACTTACGTACAAACTTACTCGGCCGCCTTCTCCCCCCGCTTCCCTCTTCTTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73292293..73292432 26863196 MeRIP-seq:(Medium) rs576048944 Functional Loss SNV dbSNP153 33..33 33 - - - 78415 RMVar_ID_78415 Human_SNP_ID_472124968 m1A Human chr11 - 73292408 73292408 73292408 GTCCATTCCTCCTCCCAGCCATTCACTCACCCATCTAGCCTGCCTTCCCTCATTCAATAGCTCAC GTCCATTCCTCCTCCCAGCCATTCACTCACCCGTCTAGCCTGCCTTCCCTCATTCAATAGCTCAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:73292289..73292521 26863196 MeRIP-seq:(Medium) rs904682622 Functional Loss SNV dbSNP153 33..33 33 - - - 78416 RMVar_ID_78416 Human_SNP_ID_472126683 m1A Human chr11 - 73298392 73298392 73298392 GGAGCATCTGGCTAACTCTTGCCCTTGTCTGGAGGGTAGCTGAAGCACAGCTCCCATTTTCTCAG GGAGCATCTGGCTAACTCTTGCCCTTGTCTGGGGGGTAGCTGAAGCACAGCTCCCATTTTCTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73298343..73298509 26863196 MeRIP-seq:(Medium) rs1321546161 Functional Loss SNV dbSNP153 33..33 33 - - - 78417 RMVar_ID_78417 Human_SNP_ID_472129393 m1A Human chr11 + 73308741 73308741 73308741 GCGGCCCCGGGCTGAGGGAGGAGGACACGGACACCCCCGGCTTGAGGCGACGCGCCTCGTGCCGG GCGGCCCCGGGCTGAGGGAGGAGGACACGGACGCCCCCGGCTTGAGGCGACGCGCCTCGTGCCGG A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73308712..73308863 26863196 MeRIP-seq:(Medium) rs946428044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868150,Human_RBP_ID_4184317,Human_RBP_ID_5139433,Human_RBP_ID_22709725 RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78418 RMVar_ID_78418 Human_SNP_ID_472129495 m1A Human chr11 - 73308935 73308934 73308935 GCCGCGGGTAAGACGCCTCCGTCTCGGGTCCCAGCGGAGCCGTCGTCCAGACGCGGCGCGTCGAA GCCGCGGGTAAGACGCCTCCGTCTCGGGTCCC_GCGGAGCCGTCGTCCAGACGCGGCGCGTCGAA CT C AP002761.3 Ensembl:ENSG00000257038 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73308886..73309031 26863196 MeRIP-seq:(Medium) rs1565182234 Functional Loss DEL dbSNP153 33..33 33 - - - 78419 RMVar_ID_78419 Human_SNP_ID_472129546 m1A Human chr11 - 73309046 73309046 73309046 GATTCAGAGTCGGCGCTGGGCCTCCTGGAGCCAGGACCGCCGAAGAGCTTGCGCATCTCGGTGAC GATTCAGAGTCGGCGCTGGGCCTCCTGGAGCCGGGACCGCCGAAGAGCTTGCGCATCTCGGTGAC T C AP002761.3 Ensembl:ENSG00000257038 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73308812..73309361 32194978 MeRIP-seq:(Medium) rs1002371241 Functional Loss SNV dbSNP153 33..33 33 - - - 78420 RMVar_ID_78420 Human_SNP_ID_472129585 m1A Human chr11 + 73309129 73309129 73309129 CGACGGTGCCGCGTGGGAGCCTCCGGCTCGGGAGTCGCGGCAGCCACCGACGCCACCCCCTCGGA CGACGGTGCCGCGTGGGAGCCTCCGGCTCGGGTGTCGCGGCAGCCACCGACGCCACCCCCTCGGA A T ARHGEF17 Ensembl:ENSG00000110237 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73308794..73309311 26863196 MeRIP-seq:(Medium) rs773106291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78421 RMVar_ID_78421 Human_SNP_ID_472129829 m1A Human chr11 + 73309579 73309579 73309579 TCAGGACTGCAGGCCTGACAGTGATGGGTTAAATCTAAGCAGCATGAACTCAGCAGGGGTTTCTG TCAGGACTGCAGGCCTGACAGTGATGGGTTAAGTCTAAGCAGCATGAACTCAGCAGGGGTTTCTG A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73309437..73309787 32194978 MeRIP-seq:(Medium) rs1369513170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866102 RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78422 RMVar_ID_78422 Human_SNP_ID_472132236 m1A Human chr11 + 73316649 73316649 73316649 AAAGGCACTGAGGTGGTTGAGAAACAGTCAAGAGAACTGTATGGATGGAGCAGAGAAGTAGAAGA AAAGGCACTGAGGTGGTTGAGAAACAGTCAAGGGAACTGTATGGATGGAGCAGAGAAGTAGAAGA A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73316429..73316796 26863196 MeRIP-seq:(Medium) rs942770568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78423 RMVar_ID_78423 Human_SNP_ID_472140116 m1A Human chr11 + 73347829 73347829 73347829 AGAAGAGGAGGTCAAGGCCATTGAGATCCGGCAAGGATAGAGGTTACAGGAAGGGAGTGCTGGGG AGAAGAGGAGGTCAAGGCCATTGAGATCCGGCCAGGATAGAGGTTACAGGAAGGGAGTGCTGGGG A C ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73347717..73348049;chr11:73347715..73348060 26863196 MeRIP-seq:(Medium) rs1371157419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41945,RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78424 RMVar_ID_78424 Human_SNP_ID_472140283 m1A Human chr11 - 73348543 73348543 73348543 CTCTGAGTCTGACTACCCCAGGAACCTCATGCAAGTGGAATCAGACAGTGCTTGTCCTTTGAGAC CTCTGAGTCTGACTACCCCAGGAACCTCATGCGAGTGGAATCAGACAGTGCTTGTCCTTTGAGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73348493..73348704 26863196 MeRIP-seq:(Medium) rs1565202525 Functional Loss SNV dbSNP153 33..33 33 - - - 78425 RMVar_ID_78425 Human_SNP_ID_472140359 m1A Human chr11 - 73348883 73348883 73348883 CCCTTCAGGTCTCAGCTAAATACCCCAACCCCAGGGAAGCCCTCCCTGACCCCGACACCAGGGTA CCCTTCAGGTCTCAGCTAAATACCCCAACCCCTGGGAAGCCCTCCCTGACCCCGACACCAGGGTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73348874..73348986 26863196 MeRIP-seq:(Medium) rs1490590371 Functional Loss SNV dbSNP153 33..33 33 - - - 78426 RMVar_ID_78426 Human_SNP_ID_472140378 m1A Human chr11 + 73348980 73348973 73348980 ATGGCTCCCAGCAGAGGGTATGTCAGGGACAAAGGCCAGGAGGCTGGAAGGAACCTAGAGCAGCA ATGGCTCCCAGCAGAGGGTATGTCAG_______GGCCAGGAGGCTGGAAGGAACCTAGAGCAGCA GGGACAAA G ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73348945..73349055 26863196 MeRIP-seq:(Medium) rs572513724 Functional Loss DEL dbSNP153 27..33 33 - - - RMVar_hsa_circ_41945,RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 78427 RMVar_ID_78427 Human_SNP_ID_472140579 m1A Human chr11 - 73349782 73349782 73349782 ACATTCTGGCTTCCTCCACCCACAGGTCCTGCACCCTCTCCCAAGTGCAGCCCTGGACGGGTCTG ACATTCTGGCTTCCTCCACCCACAGGTCCTGCGCCCTCTCCCAAGTGCAGCCCTGGACGGGTCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:73349732..73349880 26863196 MeRIP-seq:(Medium) rs1250835368 Functional Loss SNV dbSNP153 33..33 33 - - - 78428 RMVar_ID_78428 Human_SNP_ID_472142485 m1A Human chr11 + 73357099 73357099 73357099 ACGGACCTCATCGTCTGCACCACTCTGAAGCGAAAGTCAGGCTCCCTGCGGCGCAGCTCCATGAG ACGGACCTCATCGTCTGCACCACTCTGAAGCGGAAGTCAGGCTCCCTGCGGCGCAGCTCCATGAG A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73356712..73357128 32194978 MeRIP-seq:(Medium) rs1053151141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364124 Human_Splice_Rec_1276062,Human_Splice_Rec_1276063,Human_Splice_Rec_1276104,Human_Splice_Rec_1276105,Human_Splice_Rec_1276136 RMVar_hsa_circ_269817,RMVar_hsa_circ_269484,RMVar_hsa_circ_22176,RMVar_hsa_circ_48557,RMVar_hsa_circ_80224,RMVar_hsa_circ_117749,RMVar_hsa_circ_313664,RMVar_hsa_circ_96535,RMVar_hsa_circ_151596,RMVar_hsa_circ_151597,RMVar_hsa_circ_151595,RMVar_hsa_circ_302007,RMVar_hsa_circ_45309,RMVar_hsa_circ_101006,RMVar_hsa_circ_151598,RMVar_hsa_circ_75256 78429 RMVar_ID_78429 Human_SNP_ID_472144262 m1A Human chr11 + 73362854 73362854 73362854 AAAGGCATGGCGTCAGACCTCAGGATGTTAGCACACAGAGCAATGAGGGCAGGGGATGTGACACC AAAGGCATGGCGTCAGACCTCAGGATGTTAGCGCACAGAGCAATGAGGGCAGGGGATGTGACACC A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73362804..73363075 26863196 MeRIP-seq:(Medium) rs1343877668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18612653 RMVar_hsa_circ_269484,RMVar_hsa_circ_48557,RMVar_hsa_circ_80224,RMVar_hsa_circ_117749,RMVar_hsa_circ_96535,RMVar_hsa_circ_151596,RMVar_hsa_circ_151597,RMVar_hsa_circ_151595,RMVar_hsa_circ_98020,RMVar_hsa_circ_151604,RMVar_hsa_circ_81816,RMVar_hsa_circ_151603 78430 RMVar_ID_78430 Human_SNP_ID_472144802 m1A Human chr11 + 73364593 73364593 73364593 CCGAGTCCTTGTCCTGAGCCCTGACACGCTGCAGCTGGAGGTAGCAGGGGGTGGGGGAATGGAAT CCGAGTCCTTGTCCTGAGCCCTGACACGCTGCGGCTGGAGGTAGCAGGGGGTGGGGGAATGGAAT A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73364542..73364643 32194978 MeRIP-seq:(Medium) rs746363464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065275,Human_RBP_ID_18974738,Human_RBP_ID_19050283 Human_Splice_Rec_1276083,Human_Splice_Rec_1276125 RMVar_hsa_circ_269484,RMVar_hsa_circ_96535,RMVar_hsa_circ_151597,RMVar_hsa_circ_98020,RMVar_hsa_circ_151604,RMVar_hsa_circ_81816,RMVar_hsa_circ_151603,RMVar_hsa_circ_21815,RMVar_hsa_circ_21190 78431 RMVar_ID_78431 Human_SNP_ID_472144829 m1A Human chr11 + 73364673 73364673 73364673 AGCTAGGTCCGTGTGACAGGGAGATGGAGACCATGGTAGGGGCATAAGCAGCATCCAGCAGAGGG AGCTAGGTCCGTGTGACAGGGAGATGGAGACCGTGGTAGGGGCATAAGCAGCATCCAGCAGAGGG A G ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73364623..73364698 26863196 MeRIP-seq:(Medium) rs894536241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344327 RMVar_hsa_circ_269484,RMVar_hsa_circ_98020,RMVar_hsa_circ_151604,RMVar_hsa_circ_81816,RMVar_hsa_circ_151603,RMVar_hsa_circ_21815 78432 RMVar_ID_78432 Human_SNP_ID_472147810 m1A Human chr11 + 73376474 73376474 73376474 CGGGCCGCGGCGCCGAGTCGAACGGGGAGCCGAGCTGGAGCTGCCGCGGCGCAGCCAGGTAAGGA CGGGCCGCGGCGCCGAGTCGAACGGGGAGCCGGGCTGGAGCTGCCGCGGCGCAGCCAGGTAAGGA A G RELT Ensembl:ENSG00000054967 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73376424..73376530 26863196 MeRIP-seq:(Medium) rs1438438427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227491,Human_RBP_ID_4184319 Human_Splice_Rec_1276143,Human_Splice_Rec_1276163,Human_Splice_Rec_1276175 78433 RMVar_ID_78433 Human_SNP_ID_472147812 m1A Human chr11 - 73376483 73376483 73376483 CGCGCGCCCTCCTTACCTGGCTGCGCCGCGGCAGCTCCAGCTCGGCTCCCCGTTCGACTCGGCGC CGCGCGCCCTCCTTACCTGGCTGCGCCGCGGCGGCTCCAGCTCGGCTCCCCGTTCGACTCGGCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:73376434..73376531 26863196 MeRIP-seq:(Medium) rs1275444538 Functional Loss SNV dbSNP153 33..33 33 - - - 78434 RMVar_ID_78434 Human_SNP_ID_472147815 m1A Human chr11 + 73376494 73376494 73376494 AACGGGGAGCCGAGCTGGAGCTGCCGCGGCGCAGCCAGGTAAGGAGGGCGCGCGGAGCGCCCATC AACGGGGAGCCGAGCTGGAGCTGCCGCGGCGCCGCCAGGTAAGGAGGGCGCGCGGAGCGCCCATC A C RELT Ensembl:ENSG00000054967 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73376446..73376645 26863196 MeRIP-seq:(Medium) rs1055623371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227491,Human_RBP_ID_4185260,Human_RBP_ID_19052748 Human_Splice_Rec_1276143,Human_Splice_Rec_1276163,Human_Splice_Rec_1276175 78435 RMVar_ID_78435 Human_SNP_ID_472149948 m1A Human chr11 - 73385026 73385026 73385026 CCACCCTCAGGATGGCGTCGTGACGCGCCCCCACCAACCTCCCCCACCCACACGCCTGCCACGCT CCACCCTCAGGATGGCGTCGTGACGCGCCCCCCCCAACCTCCCCCACCCACACGCCTGCCACGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73385020..73385099;chr11:73385022..73385127 26863196 MeRIP-seq:(Medium) rs1396915899 Functional Loss SNV dbSNP153 33..33 33 - - - 78436 RMVar_ID_78436 Human_SNP_ID_472152031 m1A Human chr11 + 73392508 73392506 73392508 CCAGCTGGGGTCCAGGTGGGAAGGACGGGGGCACGAGCCCAGCCCCAGCTCCACTTGGGGGCTGC CCAGCTGGGGTCCAGGTGGGAAGGACGGGGG__CGAGCCCAGCCCCAGCTCCACTTGGGGGCTGC GCA G RELT Ensembl:ENSG00000054967 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73392484..73392668 26863196 MeRIP-seq:(Medium) rs1181648629 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18456959 RMVar_hsa_circ_113510,RMVar_hsa_circ_151606,RMVar_hsa_circ_14551 78437 RMVar_ID_78437 Human_SNP_ID_472152159 m1A Human chr11 + 73393039 73393039 73393039 CACACCACTACTCCCCTGCAGGGCAGGGGCCCACTCGCACACACCCTGCCCTGGGCCCATGGGAG CACACCACTACTCCCCTGCAGGGCAGGGGCCCTCTCGCACACACCCTGCCCTGGGCCCATGGGAG A T RELT Ensembl:ENSG00000054967 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73393035..73393334 32194978 MeRIP-seq:(Medium) rs1322623032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26775830 RMVar_hsa_circ_113510,RMVar_hsa_circ_151606,RMVar_hsa_circ_14551 78438 RMVar_ID_78438 Human_SNP_ID_472152549 m1A Human chr11 - 73394251 73394251 73394251 GTTTGCTGTGGTACTCTTTCAGCAGCTCCTCCAGGGCCGCAGCATTCTCTGTGGGTAGCTGCAGT GTTTGCTGTGGTACTCTTTCAGCAGCTCCTCCCGGGCCGCAGCATTCTCTGTGGGTAGCTGCAGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73394229..73394330 32194978 MeRIP-seq:(Medium) rs760234772 Functional Loss SNV dbSNP153 33..33 33 - - - 78439 RMVar_ID_78439 Human_SNP_ID_472152633 m1A Human chr11 - 73394463 73394463 73394463 CGGGGGCGCTGGCGGCAGCCTGCAGGGGGCACAGGCAGAAGTGGCCATAGGCCAGGCCAGGGGCA CGGGGGCGCTGGCGGCAGCCTGCAGGGGGCACGGGCAGAAGTGGCCATAGGCCAGGCCAGGGGCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73394456..73394577 26863196 MeRIP-seq:(Medium) rs780686583 Functional Loss SNV dbSNP153 33..33 33 - - - 78440 RMVar_ID_78440 Human_SNP_ID_472152736 m1A Human chr11 + 73394679 73394671 73394680 CCAGCCTTCTGCCTAACCCGACCAGGGTTCCCAAGGCCGGGGCCAAGGCAGGGCGTCAGGGCGAG CCAGCCTTCTGCCTAACCCGACCAG_________GGCCGGGGCCAAGGCAGGGCGTCAGGGCGAG GGGTTCCCAA G RELT Ensembl:ENSG00000054967 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73394478..73394728 32194978 MeRIP-seq:(Medium) rs1318263676 Functional Loss DEL dbSNP153 26..34 33 - - - Human_Splice_Rec_1276159,Human_Splice_Rec_1276201,Human_Splice_Rec_1276213,Human_Splice_Rec_1276219 78441 RMVar_ID_78441 Human_SNP_ID_472153104 m1A Human chr11 + 73395555 73395555 73395555 TGCCCTGGGAGGTTCCGAAGGCTTCCTGGAGGAGGTGGAGCTGCAGCTGGGACTGTGAGGACCGA TGCCCTGGGAGGTTCCGAAGGCTTCCTGGAGGTGGTGGAGCTGCAGCTGGGACTGTGAGGACCGA A T RELT Ensembl:ENSG00000054967 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr11:73395506..73395651;chr11:73395274..73395931 26863196,32194978 MeRIP-seq:(Medium) rs1362001054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403246,Human_RBP_ID_18972618 Human_miRNA_ID_159769,Human_miRNA_ID_207862,Human_miRNA_ID_706404,Human_miRNA_ID_713654,Human_miRNA_ID_1079788 78442 RMVar_ID_78442 Human_SNP_ID_472155444 m1A Human chr11 - 73405087 73405087 73405087 AGGAGAGGAAGAGGAGGAAGACAGTGGGAGTCATCAGGAGAGGAGAATGAGGATGAGGCCCAGGA AGGAGAGGAAGAGGAGGAAGACAGTGGGAGTCTTCAGGAGAGGAGAATGAGGATGAGGCCCAGGA T A FAM168A Ensembl:ENSG00000054965 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73404995..73405221 26863196 MeRIP-seq:(Medium) rs11235738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6092449,Human_RBP_ID_8176412,Human_RBP_ID_11705840,Human_RBP_ID_26408827 78443 RMVar_ID_78443 Human_SNP_ID_472156903 m1A Human chr11 - 73411447 73411447 73411447 CCCCCTACTCCCCATCACCCAACCCCTATCAGACGGCCATGTATCCAATCAGAAGTGCCTACCCC CCCCCTACTCCCCATCACCCAACCCCTATCAGGCGGCCATGTATCCAATCAGAAGTGCCTACCCC T C FAM168A Ensembl:ENSG00000054965 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73411366..73411468 26863196 MeRIP-seq:(Medium) rs764085458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17235012,Human_RBP_ID_18933863 Human_Splice_Rec_1276230,Human_Splice_Rec_1276231,Human_Splice_Rec_1276254,Human_Splice_Rec_1276255 RMVar_hsa_circ_80033,RMVar_hsa_circ_151609 78444 RMVar_ID_78444 Human_SNP_ID_472199306 m1A Human chr11 + 73596592 73596592 73596592 AAGAATGAGAAGGTCTCTTCCGTGTCCCCTGCAAAGTCCCCTCTAACAGCCTTACTGCCTCTCAC AAGAATGAGAAGGTCTCTTCCGTGTCCCCTGCGAAGTCCCCTCTAACAGCCTTACTGCCTCTCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73596590..73596897;chr11:73596583..73596951 26863196 MeRIP-seq:(Medium) rs756811642 Functional Loss SNV dbSNP153 33..33 33 - - - 78445 RMVar_ID_78445 Human_SNP_ID_472199307 m1A Human chr11 + 73596592 73596592 73596592 AAGAATGAGAAGGTCTCTTCCGTGTCCCCTGCAAAGTCCCCTCTAACAGCCTTACTGCCTCTCAC AAGAATGAGAAGGTCTCTTCCGTGTCCCCTGCTAAGTCCCCTCTAACAGCCTTACTGCCTCTCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73596590..73596897;chr11:73596583..73596951 26863196 MeRIP-seq:(Medium) rs756811642 Functional Loss SNV dbSNP153 33..33 33 - - - 78446 RMVar_ID_78446 Human_SNP_ID_472199418 m1A Human chr11 + 73597097 73597097 73597097 GATCACCCTAAATCCAACCCACTGTGCCCCACACTCCATTTCCATCCCTGTCCTCCCATTTCGGG GATCACCCTAAATCCAACCCACTGTGCCCCACGCTCCATTTCCATCCCTGTCCTCCCATTTCGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:73597092..73597223 26863196 MeRIP-seq:(Medium) rs899759361 Functional Loss SNV dbSNP153 33..33 33 - - - 78447 RMVar_ID_78447 Human_SNP_ID_472242661 m1A Human chr11 + 73761031 73761031 73761031 ACGTATCTGGGACCTCTCACGCGCAGCGCCTGAGCTTCCACAGCTGCCGCCGCCGCCGCAGCCCA ACGTATCTGGGACCTCTCACGCGCAGCGCCTGGGCTTCCACAGCTGCCGCCGCCGCCGCAGCCCA A G AP002770.1 Ensembl:ENSG00000256034 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73760931..73761071;chr11:73760927..73761036 26863196 MeRIP-seq:(Medium) rs997640099 Functional Loss SNV dbSNP153 33..33 33 - - - 78448 RMVar_ID_78448 Human_SNP_ID_472242665 m1A Human chr11 - 73761034 73761034 73761034 GGTTGGGCTGCGGCGGCGGCGGCAGCTGTGGAAGCTCAGGCGCTGCGCGTGAGAGGTCCCAGATA GGTTGGGCTGCGGCGGCGGCGGCAGCTGTGGAGGCTCAGGCGCTGCGCGTGAGAGGTCCCAGATA T C RAB6A Ensembl:ENSG00000175582 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:73760895..73761046;chr11:73760930..73761036 26863196 MeRIP-seq:(Medium) rs1335659379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227158,Human_RBP_ID_4184323,Human_RBP_ID_5138734,Human_RBP_ID_5314409,Human_RBP_ID_9276049 RMVar_hsa_circ_127239,RMVar_hsa_circ_93443,RMVar_hsa_circ_151623,RMVar_hsa_circ_151633 78449 RMVar_ID_78449 Human_SNP_ID_472250004 m1A Human chr11 + 73787944 73787944 73787944 AACGCGGCTGCAGGGTCCGGTCTTCGGTTTGCACAGCTAGAGGCCGCGCAGCAGCAAAGGATGAG AACGCGGCTGCAGGGTCCGGTCTTCGGTTTGCGCAGCTAGAGGCCGCGCAGCAGCAAAGGATGAG A G MRPL48 Ensembl:ENSG00000175581 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73787909..73788054 26863196 MeRIP-seq:(Medium) rs780429518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403429,Human_RBP_ID_4185269,Human_RBP_ID_5490320 Human_Splice_Rec_1276583,Human_Splice_Rec_1276599,Human_Splice_Rec_1276613,Human_Splice_Rec_1276629,Human_Splice_Rec_1276637,Human_Splice_Rec_1276649,Human_Splice_Rec_1276659,Human_Splice_Rec_1276677,Human_Splice_Rec_1276687,Human_Splice_Rec_1276701,Human_Splice_Rec_1276711,Human_Splice_Rec_1276715 Human_miRNA_ID_1968610,Human_miRNA_ID_2180965,Human_miRNA_ID_2183067 RMVar_hsa_circ_120733,RMVar_hsa_circ_151637 78450 RMVar_ID_78450 Human_SNP_ID_472251375 m1A Human chr11 - 73793647 73793647 73793647 TAATCTACACCCCAGTGCTTCTCTCCCTCCCAACTTCCTCTAGGAGTTCCTCTGGAACTCCAAGT TAATCTACACCCCAGTGCTTCTCTCCCTCCCAGCTTCCTCTAGGAGTTCCTCTGGAACTCCAAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73793644..73793727 26863196 MeRIP-seq:(Medium) rs954578682 Functional Loss SNV dbSNP153 33..33 33 - - - 78451 RMVar_ID_78451 Human_SNP_ID_472255655 m1A Human chr11 - 73811275 73811275 73811275 TAATTTCCACAACCCATCCACCCCACCTACCTAGACTACCCTCCCTAAGGTCACCAGTGACCTCT TAATTTCCACAACCCATCCACCCCACCTACCTCGACTACCCTCCCTAAGGTCACCAGTGACCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73811271..73811398 26863196 MeRIP-seq:(Medium) rs1022474026 Functional Loss SNV dbSNP153 33..33 33 - - - 78452 RMVar_ID_78452 Human_SNP_ID_472269733 m1A Human chr11 + 73873152 73873152 73873152 GGTGGGCACCGGCTTGTTCTTGCCTCCTCTGCAGCTCCTCTTGCCGCCTCGCCTGCTGTTCACTC GGTGGGCACCGGCTTGTTCTTGCCTCCTCTGCGGCTCCTCTTGCCGCCTCGCCTGCTGTTCACTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:73872826..73873350;chr11:73873076..73873415 32194978 MeRIP-seq:(Medium) rs141027407 Functional Loss SNV dbSNP153 33..33 33 - - - 78453 RMVar_ID_78453 Human_SNP_ID_472269795 m1A Human chr11 - 73873330 73873324 73873330 CTCAAGGCCATACCTGGACCCAACGGGTGAAGAAAGACGATGAGGAGGAGGACCCGCTGGACCAG CTCAAGGCCATACCTGGACCCAACGGGTGAAG______GATGAGGAGGAGGACCCGCTGGACCAG CGTCTTT C COA4 Ensembl:ENSG00000181924 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73873048..73873426 26863196 MeRIP-seq:(Medium) rs1565118460 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_1460214,Human_RBP_ID_4178277,Human_RBP_ID_22433185,Human_RBP_ID_22895589,Human_RBP_ID_23520635,Human_RBP_ID_27416050 Human_Splice_Rec_1276738,Human_Splice_Rec_1276740,Human_Splice_Rec_1276744 RMVar_hsa_circ_101662,RMVar_hsa_circ_151643 78454 RMVar_ID_78454 Human_SNP_ID_472269795 m1A Human chr11 - 73873329 73873324 73873330 TCAAGGCCATACCTGGACCCAACGGGTGAAGAAAGACGATGAGGAGGAGGACCCGCTGGACCAGC TCAAGGCCATACCTGGACCCAACGGGTGAAG______GATGAGGAGGAGGACCCGCTGGACCAGC CGTCTTT C COA4 Ensembl:ENSG00000181924 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:73872948..73873415 26863196 MeRIP-seq:(Medium) rs1565118460 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_1460214,Human_RBP_ID_4178277,Human_RBP_ID_22433185,Human_RBP_ID_22895589,Human_RBP_ID_23520635,Human_RBP_ID_27416050 Human_Splice_Rec_1276738,Human_Splice_Rec_1276740,Human_Splice_Rec_1276744 RMVar_hsa_circ_101662,RMVar_hsa_circ_151643 78455 RMVar_ID_78455 Human_SNP_ID_472269801 m1A Human chr11 + 73873335 73873335 73873335 CCAGCGGGTCCTCCTCCTCATCGTCTTTCTTCACCCGTTGGGTCCAGGTATGGCCTTGAGGGACT CCAGCGGGTCCTCCTCCTCATCGTCTTTCTTCGCCCGTTGGGTCCAGGTATGGCCTTGAGGGACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:73873026..73873421 26863196 MeRIP-seq:(Medium) rs756006210 Functional Loss SNV dbSNP153 33..33 33 - - - 78456 RMVar_ID_78456 Human_SNP_ID_472269816 m1A Human chr11 - 73873367 73873367 73873367 TATAGACTCCCCATCCCCAGGATGTCAACCTCAGTCCCTCAAGGCCATACCTGGACCCAACGGGT TATAGACTCCCCATCCCCAGGATGTCAACCTCGGTCCCTCAAGGCCATACCTGGACCCAACGGGT T C COA4 Ensembl:ENSG00000181924 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:73873009..73873427 26863196 MeRIP-seq:(Medium) rs1452562365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750639,Human_RBP_ID_988357,Human_RBP_ID_1460214,Human_RBP_ID_4186204,Human_RBP_ID_5460813,Human_RBP_ID_5490324,Human_RBP_ID_22895761,Human_RBP_ID_23520636 Human_Splice_Rec_1276738,Human_Splice_Rec_1276740,Human_Splice_Rec_1276744 Human_miRNA_ID_2351780,Human_miRNA_ID_3047328 RMVar_hsa_circ_101662,RMVar_hsa_circ_151643 78457 RMVar_ID_78457 Human_SNP_ID_472269832 m1A Human chr11 - 73873394 73873394 73873394 TATCCCTACTCTAACCTGTTAATGTTCTATAGACTCCCCATCCCCAGGATGTCAACCTCAGTCCC TATCCCTACTCTAACCTGTTAATGTTCTATAGGCTCCCCATCCCCAGGATGTCAACCTCAGTCCC T C COA4 Ensembl:ENSG00000181924 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:73873315..73873415 26863410 MeRIP-seq:(Medium) rs781197097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178283,Human_RBP_ID_5460813 Human_Splice_Rec_1276738,Human_Splice_Rec_1276740,Human_Splice_Rec_1276744 Human_miRNA_ID_2040200,Human_miRNA_ID_2367283,Human_miRNA_ID_3015081,Human_miRNA_ID_3019182 RMVar_hsa_circ_101662,RMVar_hsa_circ_151643 78458 RMVar_ID_78458 Human_SNP_ID_472269833 m1A Human chr11 - 73873396 73873396 73873396 TATATCCCTACTCTAACCTGTTAATGTTCTATAGACTCCCCATCCCCAGGATGTCAACCTCAGTC TATATCCCTACTCTAACCTGTTAATGTTCTATTGACTCCCCATCCCCAGGATGTCAACCTCAGTC T A COA4 Ensembl:ENSG00000181924 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:73873364..73873465 32194978 MeRIP-seq:(Medium) rs112512731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178284 78459 RMVar_ID_78459 Human_SNP_ID_472269834 m1A Human chr11 - 73873396 73873396 73873396 TATATCCCTACTCTAACCTGTTAATGTTCTATAGACTCCCCATCCCCAGGATGTCAACCTCAGTC TATATCCCTACTCTAACCTGTTAATGTTCTATCGACTCCCCATCCCCAGGATGTCAACCTCAGTC T G COA4 Ensembl:ENSG00000181924 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:73873364..73873465 32194978 MeRIP-seq:(Medium) rs112512731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178284 78460 RMVar_ID_78460 Human_SNP_ID_472270625 m1A Human chr11 + 73876657 73876655 73876657 GCCACGAGGCCTGAGGCGCCTCAGGCGTATCGAGGACTTTGAACTTTGAGGACGCATGCGCGCGC GCCACGAGGCCTGAGGCGCCTCAGGCGTATC__GGACTTTGAACTTTGAGGACGCATGCGCGCGC CGA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:73876652..73876732 32194978 MeRIP-seq:(Medium) rs1229750635 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11709540 Human_Splice_Rec_1276749 78461 RMVar_ID_78461 Human_SNP_ID_472270656 m1A Human chr11 - 73876715 73876715 73876715 GCGTACCGCGTTCTTCAGGAGGCGTTGCGGGCACAACGGGGCTGCGATCAGCGGCCGCGCGCGCG GCGTACCGCGTTCTTCAGGAGGCGTTGCGGGCCCAACGGGGCTGCGATCAGCGGCCGCGCGCGCG T G COA4 Ensembl:ENSG00000181924 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:73876713..73876824 26863410 MeRIP-seq:(Medium) rs1383201359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19050291 78462 RMVar_ID_78462 Human_SNP_ID_472270700 m1A Human chr11 - 73876806 73876806 73876806 GTACAGAGGATCCCCAACCGCCTGCGAAACCCAAGCCGCCGCGTAGGAGCGTGCGTTCGGGCCCT GTACAGAGGATCCCCAACCGCCTGCGAAACCCTAGCCGCCGCGTAGGAGCGTGCGTTCGGGCCCT T A COA4 Ensembl:ENSG00000181924 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:73876504..73876875;chr11:73876556..73876875;chr11:73876694..73876875 26863196 MeRIP-seq:(Medium) rs960355293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178291,Human_RBP_ID_9321731,Human_RBP_ID_21883646 Human_Splice_Rec_1276737,Human_Splice_Rec_1276741,Human_Splice_Rec_1276747 78463 RMVar_ID_78463 Human_SNP_ID_472270701 m1A Human chr11 - 73876806 73876806 73876806 GTACAGAGGATCCCCAACCGCCTGCGAAACCCAAGCCGCCGCGTAGGAGCGTGCGTTCGGGCCCT GTACAGAGGATCCCCAACCGCCTGCGAAACCCCAGCCGCCGCGTAGGAGCGTGCGTTCGGGCCCT T G COA4 Ensembl:ENSG00000181924 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:73876504..73876875;chr11:73876556..73876875;chr11:73876694..73876875 26863196 MeRIP-seq:(Medium) rs960355293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178291,Human_RBP_ID_9321731,Human_RBP_ID_21883646 Human_Splice_Rec_1276737,Human_Splice_Rec_1276741,Human_Splice_Rec_1276747 78464 RMVar_ID_78464 Human_SNP_ID_472296309 m1A Human chr11 - 73976744 73976744 73976744 TCTGGTCTCACCCAGGATCTTCCTCCTCCTACAGGGACCTCTCCCAATGTTGCTCGTAATGCCAT TCTGGTCTCACCCAGGATCTTCCTCCTCCTACCGGGACCTCTCCCAATGTTGCTCGTAATGCCAT T G UCP2 Ensembl:ENSG00000175567 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:73976701..73976981 32194978 MeRIP-seq:(Medium) rs758560067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3118,Human_RBP_ID_868164,Human_RBP_ID_5341807,Human_RBP_ID_22641886 RMVar_hsa_circ_89773,RMVar_hsa_circ_125553,RMVar_hsa_circ_105325,RMVar_hsa_circ_112974,RMVar_hsa_circ_151651,RMVar_hsa_circ_151653,RMVar_hsa_circ_89288,RMVar_hsa_circ_151654,RMVar_hsa_circ_151652,RMVar_hsa_circ_28654,RMVar_hsa_circ_151650 78465 RMVar_ID_78465 Human_SNP_ID_472297880 m1A Human chr11 + 73982786 73982786 73982786 CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGACGAGCCGGGCGAGCGTGGACAGTCAATCCCAA CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGCCGAGCCGGGCGAGCGTGGACAGTCAATCCCAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73981551..73982850;chr11:73982679..73982814;chr11:73982738..73982822;chr11:73982711..73982803 26863196 MeRIP-seq:(Medium) rs535760193 Functional Loss SNV dbSNP153 33..33 33 - - - 78466 RMVar_ID_78466 Human_SNP_ID_472297881 m1A Human chr11 + 73982786 73982786 73982786 CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGACGAGCCGGGCGAGCGTGGACAGTCAATCCCAA CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGGCGAGCCGGGCGAGCGTGGACAGTCAATCCCAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73981551..73982850;chr11:73982679..73982814;chr11:73982738..73982822;chr11:73982711..73982803 26863196 MeRIP-seq:(Medium) rs535760193 Functional Loss SNV dbSNP153 33..33 33 - - - 78467 RMVar_ID_78467 Human_SNP_ID_472297882 m1A Human chr11 + 73982786 73982786 73982786 CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGACGAGCCGGGCGAGCGTGGACAGTCAATCCCAA CTGTGTCTGTCGGCTGGCGGAGGGCGCGTCGGTCGAGCCGGGCGAGCGTGGACAGTCAATCCCAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:73981551..73982850;chr11:73982679..73982814;chr11:73982738..73982822;chr11:73982711..73982803 26863196 MeRIP-seq:(Medium) rs535760193 Functional Loss SNV dbSNP153 33..33 33 - - - 78468 RMVar_ID_78468 Human_SNP_ID_472343417 m1A Human chr11 + 74170834 74170829 74170835 GAGCTCTTCTTCACCAGCTCAACTCCGTCTCCAGCACCTAAGCAGTATCCTCCCGCCATCCCTCC GAGCTCTTCTTCACCAGCTCAACTCCGT______CACCTAAGCAGTATCCTCCCGCCATCCCTCC TCTCCAG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74170783..74170861 26863196 MeRIP-seq:(Medium) rs1288977518 Functional Loss DEL dbSNP153 29..34 33 - - - 78469 RMVar_ID_78469 Human_SNP_ID_472343419 m1A Human chr11 + 74170834 74170834 74170834 GAGCTCTTCTTCACCAGCTCAACTCCGTCTCCAGCACCTAAGCAGTATCCTCCCGCCATCCCTCC GAGCTCTTCTTCACCAGCTCAACTCCGTCTCCGGCACCTAAGCAGTATCCTCCCGCCATCCCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74170783..74170861 26863196 MeRIP-seq:(Medium) rs1221770501 Functional Loss SNV dbSNP153 33..33 33 - - - 78470 RMVar_ID_78470 Human_SNP_ID_472344040 m1A Human chr11 + 74172906 74172906 74172906 AATATGTGTAAAAACTTATCAAAAAGGAGGCGAGAGTAGGAGATGCAGTACTGTGACAGTAAGTC AATATGTGTAAAAACTTATCAAAAAGGAGGCGGGAGTAGGAGATGCAGTACTGTGACAGTAAGTC A G PPME1 Ensembl:ENSG00000214517 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:74172883..74173039 26863196 MeRIP-seq:(Medium) rs1293682060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17801043 RMVar_hsa_circ_127618,RMVar_hsa_circ_151705,RMVar_hsa_circ_151704 78471 RMVar_ID_78471 Human_SNP_ID_472352866 m1A Human chr11 - 74212182 74212181 74212183 CAATCACTGTGCTCTCCCTCCCACAAGCACACAGATTCTCTCTCCGTTCCACGCAACCACTGCCA CAATCACTGTGCTCTCCCTCCCACAAGCACA__GATTCTCTCTCCGTTCCACGCAACCACTGCCA CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:74212165..74212286 26863196 MeRIP-seq:(Medium) rs780874576 Functional Loss DEL dbSNP153 32..33 33 - - - 78472 RMVar_ID_78472 Human_SNP_ID_472357974 m1A Human chr11 + 74235922 74235922 74235922 TTCTTTCCCAGTGTGAAGAGTGGCCAGATTCGAAATCTGGAGTCTGCCCGTGTCTCAATGGTTGG TTCTTTCCCAGTGTGAAGAGTGGCCAGATTCGTAATCTGGAGTCTGCCCGTGTCTCAATGGTTGG A T P4HA3 Ensembl:ENSG00000149380 Protein coding exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs746733509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1277494 78473 RMVar_ID_78473 Human_SNP_ID_472375604 m1A Human chr11 - 74311509 74311509 74311509 CTGCGGCTCGGGGCGACACGTTCTCGGCGCTGACCAGCGTGGCGCGCGCCCTGGCGCCCGAGCGC CTGCGGCTCGGGGCGACACGTTCTCGGCGCTGTCCAGCGTGGCGCGCGCCCTGGCGCCCGAGCGC T A P4HA3 Ensembl:ENSG00000149380 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:74311472..74311655 26863196 MeRIP-seq:(Medium) rs750727191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1277495,Human_Splice_Rec_1277531,Human_Splice_Rec_1277553,Human_Splice_Rec_1277577 78474 RMVar_ID_78474 Human_SNP_ID_472375605 m1A Human chr11 - 74311509 74311509 74311509 CTGCGGCTCGGGGCGACACGTTCTCGGCGCTGACCAGCGTGGCGCGCGCCCTGGCGCCCGAGCGC CTGCGGCTCGGGGCGACACGTTCTCGGCGCTGGCCAGCGTGGCGCGCGCCCTGGCGCCCGAGCGC T C P4HA3 Ensembl:ENSG00000149380 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:74311472..74311655 26863196 MeRIP-seq:(Medium) rs750727191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1277495,Human_Splice_Rec_1277531,Human_Splice_Rec_1277553,Human_Splice_Rec_1277577 78475 RMVar_ID_78475 Human_SNP_ID_472380655 m1A Human chr11 + 74333902 74333902 74333902 ATGAGAATGCAATCATTTTCACAATATTGTTCAAAAAGAAAAAGATAAACATTGTAGTGCCCGAG ATGAGAATGCAATCATTTTCACAATATTGTTCCAAAAGAAAAAGATAAACATTGTAGTGCCCGAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:74333851..74333947 32194978 MeRIP-seq:(Medium) rs574340129 Functional Loss SNV dbSNP153 33..33 33 - - - 78476 RMVar_ID_78476 Human_SNP_ID_472394875 m1A Human chr11 - 74398319 74398319 74398319 CGGCCATAAACCCCCTCTCTCCCGGTTCCCTGACGCCGCGGCAGGAGCTGTTACGAACACCCTGC CGGCCATAAACCCCCTCTCTCCCGGTTCCCTGCCGCCGCGGCAGGAGCTGTTACGAACACCCTGC T G PGM2L1 Ensembl:ENSG00000165434 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:74398273..74398406 26863196 MeRIP-seq:(Medium) rs1019008853 Functional Loss SNV dbSNP153 33..33 33 - - - 78477 RMVar_ID_78477 Human_SNP_ID_472417172 m1A Human chr11 + 74493477 74493476 74493477 CACCGCGGCCTGTGACGCGCACCTCGGCGCCCAAGGCCCGTAGCCGCGCAGTTTCCTCGGGCGTC CACCGCGGCCTGTGACGCGCACCTCGGCGCCC_AGGCCCGTAGCCGCGCAGTTTCCTCGGGCGTC CA C AP001372.2 Ensembl:ENSG00000254837 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:74493427..74493668 26863196 MeRIP-seq:(Medium) rs1403400504 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4187086 78478 RMVar_ID_78478 Human_SNP_ID_472440432 m1A Human chr11 + 74592645 74592645 74592645 TGTGATTGAGAGAGGGGTTAGAGGCGGGTCCCAGCGCTGCCGCACCATGGCGGACCAGCTTTATC TGTGATTGAGAGAGGGGTTAGAGGCGGGTCCCCGCGCTGCCGCACCATGGCGGACCAGCTTTATC A C POLD3 Ensembl:ENSG00000077514 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:74592595..74592950;chr11:74592597..74595155 26863196 MeRIP-seq:(Medium) rs777458521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226252,Human_RBP_ID_18416629 Human_Splice_Rec_1277707,Human_Splice_Rec_1277711,Human_Splice_Rec_1277755 RMVar_hsa_circ_92338,RMVar_hsa_circ_151738 78479 RMVar_ID_78479 Human_SNP_ID_472440433 m1A Human chr11 + 74592645 74592645 74592645 TGTGATTGAGAGAGGGGTTAGAGGCGGGTCCCAGCGCTGCCGCACCATGGCGGACCAGCTTTATC TGTGATTGAGAGAGGGGTTAGAGGCGGGTCCCGGCGCTGCCGCACCATGGCGGACCAGCTTTATC A G POLD3 Ensembl:ENSG00000077514 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:74592595..74592950;chr11:74592597..74595155 26863196 MeRIP-seq:(Medium) rs777458521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226252,Human_RBP_ID_18416629 Human_Splice_Rec_1277707,Human_Splice_Rec_1277711,Human_Splice_Rec_1277755 RMVar_hsa_circ_92338,RMVar_hsa_circ_151738 78480 RMVar_ID_78480 Human_SNP_ID_472440436 m1A Human chr11 - 74592650 74592650 74592650 TTCCAGATAAAGCTGGTCCGCCATGGTGCGGCAGCGCTGGGACCCGCCTCTAACCCCTCTCTCAA TTCCAGATAAAGCTGGTCCGCCATGGTGCGGCCGCGCTGGGACCCGCCTCTAACCCCTCTCTCAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74592599..74592764 26863196 MeRIP-seq:(Medium) rs746786149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17682613 78481 RMVar_ID_78481 Human_SNP_ID_472450694 m1A Human chr11 + 74634607 74634607 74634607 TATTTCAGTCTTTCCAGACTCTCCTGGGGCTTATGAAGCTGAGTCACCATCCCCACCTCCTCCTC TATTTCAGTCTTTCCAGACTCTCCTGGGGCTTCTGAAGCTGAGTCACCATCCCCACCTCCTCCTC A C POLD3 Ensembl:ENSG00000077514 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:74634597..74640620 32194978 MeRIP-seq:(Medium) rs1186843578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403597,Human_RBP_ID_988369,Human_RBP_ID_11711816 Human_Splice_Rec_1277728,Human_Splice_Rec_1277729,Human_Splice_Rec_1277750,Human_Splice_Rec_1277751,Human_Splice_Rec_1277770,Human_Splice_Rec_1277771,Human_Splice_Rec_1277794,Human_Splice_Rec_1277795,Human_Splice_Rec_1277800,Human_Splice_Rec_1277801 Human_miRNA_ID_1957126 RMVar_hsa_circ_92652,RMVar_hsa_circ_70340,RMVar_hsa_circ_34364,RMVar_hsa_circ_61672,RMVar_hsa_circ_151739,RMVar_hsa_circ_82284,RMVar_hsa_circ_62768,RMVar_hsa_circ_151741,RMVar_hsa_circ_98683,RMVar_hsa_circ_151742,RMVar_hsa_circ_114708,RMVar_hsa_circ_119457,RMVar_hsa_circ_151743,RMVar_hsa_circ_123870,RMVar_hsa_circ_151744,RMVar_hsa_circ_151746,RMVar_hsa_circ_151745,RMVar_hsa_circ_334662 78482 RMVar_ID_78482 Human_SNP_ID_472450695 m1A Human chr11 + 74634607 74634607 74634607 TATTTCAGTCTTTCCAGACTCTCCTGGGGCTTATGAAGCTGAGTCACCATCCCCACCTCCTCCTC TATTTCAGTCTTTCCAGACTCTCCTGGGGCTTTTGAAGCTGAGTCACCATCCCCACCTCCTCCTC A T POLD3 Ensembl:ENSG00000077514 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:74634597..74640620 32194978 MeRIP-seq:(Medium) rs1186843578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403597,Human_RBP_ID_988369,Human_RBP_ID_11711816 Human_Splice_Rec_1277728,Human_Splice_Rec_1277729,Human_Splice_Rec_1277750,Human_Splice_Rec_1277751,Human_Splice_Rec_1277770,Human_Splice_Rec_1277771,Human_Splice_Rec_1277794,Human_Splice_Rec_1277795,Human_Splice_Rec_1277800,Human_Splice_Rec_1277801 Human_miRNA_ID_1957126 RMVar_hsa_circ_92652,RMVar_hsa_circ_70340,RMVar_hsa_circ_34364,RMVar_hsa_circ_61672,RMVar_hsa_circ_151739,RMVar_hsa_circ_82284,RMVar_hsa_circ_62768,RMVar_hsa_circ_151741,RMVar_hsa_circ_98683,RMVar_hsa_circ_151742,RMVar_hsa_circ_114708,RMVar_hsa_circ_119457,RMVar_hsa_circ_151743,RMVar_hsa_circ_123870,RMVar_hsa_circ_151744,RMVar_hsa_circ_151746,RMVar_hsa_circ_151745,RMVar_hsa_circ_334662 78483 RMVar_ID_78483 Human_SNP_ID_472452126 m1A Human chr11 - 74640769 74640769 74640769 CCACTCCAAGTCTCTGATCTACCAGAGATGGCAGTTTATTTCCTCTGGAAGAAGCCAGTAATGGA CCACTCCAAGTCTCTGATCTACCAGAGATGGCTGTTTATTTCCTCTGGAAGAAGCCAGTAATGGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:74640718..74640818 32194978 MeRIP-seq:(Medium) rs936867898 Functional Loss SNV dbSNP153 33..33 33 - - - 78484 RMVar_ID_78484 Human_SNP_ID_472452396 m1A Human chr11 - 74642048 74642048 74642048 ACACCCCTTGTCTGCTACGTGTGAGACACATCAGCAGTTGAGCCTGACCCCTTCCGCAGAGCTCA ACACCCCTTGTCTGCTACGTGTGAGACACATCGGCAGTTGAGCCTGACCCCTTCCGCAGAGCTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:74641859..74642108 32194978 MeRIP-seq:(Medium) rs1233886239 Functional Loss SNV dbSNP153 33..33 33 - - - 78485 RMVar_ID_78485 Human_SNP_ID_472477170 m1A Human chr11 - 74748934 74748932 74748934 TCACAGCGGCCCCGCCGGCCCCGCCGACTCAGAGCGGCTGCTGCCGCCGCGGAAGAGGCCCGAGT TCACAGCGGCCCCGCCGGCCCCGCCGACTCAG__CGGCTGCTGCCGCCGCGGAAGAGGCCCGAGT GCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74748888..74748999 26863196 MeRIP-seq:(Medium) rs1565166195 Functional Loss DEL dbSNP153 33..34 33 - - - 78486 RMVar_ID_78486 Human_SNP_ID_472525614 m1A Human chr11 - 74949038 74949038 74949038 GTTACTAAGGCGTGGGGAAGATAGCGGCAGGCACCGCAGTGGAGCGGCTCCGAGATCCCCGGGGG GTTACTAAGGCGTGGGGAAGATAGCGGCAGGCCCCGCAGTGGAGCGGCTCCGAGATCCCCGGGGG T G XRRA1 Ensembl:ENSG00000166435 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74948933..74949058 26863196 MeRIP-seq:(Medium) rs61745466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808088,Human_RBP_ID_4185279,Human_RBP_ID_27803825 RMVar_hsa_circ_87966,RMVar_hsa_circ_151770 78487 RMVar_ID_78487 Human_SNP_ID_472525617 m1A Human chr11 - 74949042 74949042 74949042 CGCAGTTACTAAGGCGTGGGGAAGATAGCGGCAGGCACCGCAGTGGAGCGGCTCCGAGATCCCCG CGCAGTTACTAAGGCGTGGGGAAGATAGCGGCGGGCACCGCAGTGGAGCGGCTCCGAGATCCCCG T C XRRA1 Ensembl:ENSG00000166435 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:74948926..74949079;chr11:74948963..74949055 26863196 MeRIP-seq:(Medium) rs1178065769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808088,Human_RBP_ID_4185279,Human_RBP_ID_27803825 RMVar_hsa_circ_87966,RMVar_hsa_circ_151770 78488 RMVar_ID_78488 Human_SNP_ID_472525777 m1A Human chr11 + 74949367 74949367 74949367 GTAGTGGGGCTGGTGGTGCTTCCAACTGCGGGACAGGAAGTGGCCGTAGCGGCTTGTTGGATAAG GTAGTGGGGCTGGTGGTGCTTCCAACTGCGGGGCAGGAAGTGGCCGTAGCGGCTTGTTGGATAAG A G SPCS2 Ensembl:ENSG00000118363 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:74949276..74949419 26863196 MeRIP-seq:(Medium) rs1215051875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403690,Human_RBP_ID_4194720,Human_RBP_ID_18416631,Human_RBP_ID_22433866 Human_Splice_Rec_1278237,Human_Splice_Rec_1278243,Human_Splice_Rec_1278249,Human_Splice_Rec_1278255,Human_Splice_Rec_1278263,Human_Splice_Rec_1278269,Human_Splice_Rec_1278273 78489 RMVar_ID_78489 Human_SNP_ID_472525779 m1A Human chr11 + 74949372 74949372 74949372 GGGGCTGGTGGTGCTTCCAACTGCGGGACAGGAAGTGGCCGTAGCGGCTTGTTGGATAAGGTGAG GGGGCTGGTGGTGCTTCCAACTGCGGGACAGGGAGTGGCCGTAGCGGCTTGTTGGATAAGGTGAG A G SPCS2 Ensembl:ENSG00000118363 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:74949276..74949437 26863410 MeRIP-seq:(Medium) rs61749533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403690,Human_RBP_ID_4194720,Human_RBP_ID_18416631,Human_RBP_ID_22433866 Human_Splice_Rec_1278237,Human_Splice_Rec_1278243,Human_Splice_Rec_1278249,Human_Splice_Rec_1278255,Human_Splice_Rec_1278263,Human_Splice_Rec_1278269,Human_Splice_Rec_1278273 78490 RMVar_ID_78490 Human_SNP_ID_472529486 m1A Human chr11 + 74964936 74964934 74964937 AGTTCTGCAACATCAGAAGACAAAGAGTAAATATTATATGTGCATGAGGGATGCTCTTAAAAAAT AGTTCTGCAACATCAGAAGACAAAGAGTAAA___TATATGTGCATGAGGGATGCTCTTAAAAAAT ATAT A SPCS2 Ensembl:ENSG00000118363 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:74964910..74965053 26863196 MeRIP-seq:(Medium) rs1361078248 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_19257 78491 RMVar_ID_78491 Human_SNP_ID_472604202 m1A Human chr11 - 75280960 75280960 75280960 CAATACCTGGAAGTGTGTGAGGAGGGGCGCACATTCCAGCCTTGGAAGGGCACTCTGGAAGCTGG CAATACCTGGAAGTGTGTGAGGAGGGGCGCACCTTCCAGCCTTGGAAGGGCACTCTGGAAGCTGG T G ARRB1 Ensembl:ENSG00000137486 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75280958..75281067 26863196 MeRIP-seq:(Medium) rs1381781966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5344343 RMVar_hsa_circ_49183,RMVar_hsa_circ_114324,RMVar_hsa_circ_151780,RMVar_hsa_circ_82041,RMVar_hsa_circ_151782 78492 RMVar_ID_78492 Human_SNP_ID_472621348 m1A Human chr11 + 75351519 75351519 75351519 TGGCCGCGAACGCAGAACCAGGACGCAATCGGAGCCCCCGCCCGTGTCCTCGCCGAGGTCGCCCC TGGCCGCGAACGCAGAACCAGGACGCAATCGGGGCCCCCGCCCGTGTCCTCGCCGAGGTCGCCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75351515..75351816 26863196 MeRIP-seq:(Medium) rs1444671820 Functional Loss SNV dbSNP153 33..33 33 - - - 78493 RMVar_ID_78493 Human_SNP_ID_472634182 m1A Human chr11 - 75400677 75400673 75400678 TGCCATCAGCGACAAACTAATCCAAACAAAGCAAAGTTCAAAATTAGGAGATCGGTGTAGGCTCA TGCCATCAGCGACAAACTAATCCAAACAAAG_____TTCAAAATTAGGAGATCGGTGTAGGCTCA ACTTTG A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:75400675..75400867 26863410 MeRIP-seq:(Medium) rs760831658 Functional Loss DEL dbSNP153 32..36 33 - - - 78494 RMVar_ID_78494 Human_SNP_ID_472634186 m1A Human chr11 - 75400681 75400681 75400681 AAGATGCCATCAGCGACAAACTAATCCAAACAAAGCAAAGTTCAAAATTAGGAGATCGGTGTAGG AAGATGCCATCAGCGACAAACTAATCCAAACACAGCAAAGTTCAAAATTAGGAGATCGGTGTAGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr11:75400676..75400725;chr11:75400676..75401725;chr11:75400676..75400825 26863196,32194978 MeRIP-seq:(Medium) rs755820749 Functional Loss SNV dbSNP153 33..33 33 - - - 78495 RMVar_ID_78495 Human_SNP_ID_472634211 m1A Human chr11 + 75400771 75400771 75400771 ACTCGGGAGCTGGCTGAAGATGGCTACTCTGGAGTTGAGGTGCGAGTTACACCAACCAGGACAGA ACTCGGGAGCTGGCTGAAGATGGCTACTCTGGGGTTGAGGTGCGAGTTACACCAACCAGGACAGA A G RPS3 Ensembl:ENSG00000149273 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75400514..75400833 26863196 MeRIP-seq:(Medium) rs370158932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30798,Human_RBP_ID_403773,Human_RBP_ID_807542,Human_RBP_ID_869289,Human_RBP_ID_1460303,Human_RBP_ID_1782616,Human_RBP_ID_3380217,Human_RBP_ID_4178797,Human_RBP_ID_5165749,Human_RBP_ID_5550261,Human_RBP_ID_6094998,Human_RBP_ID_8358985,Human_RBP_ID_8771915,Human_RBP_ID_9006378,Human_RBP_ID_9322310,Human_RBP_ID_11716204,Human_RBP_ID_17062346,Human_RBP_ID_17648471,Human_RBP_ID_17683071,Human_RBP_ID_17801333,Human_RBP_ID_18252377,Human_RBP_ID_18612980,Human_RBP_ID_22433870,Human_RBP_ID_22792218,Human_RBP_ID_22893930,Human_RBP_ID_23207039,Human_RBP_ID_23521405,Human_RBP_ID_24550875,Human_RBP_ID_26407119,Human_RBP_ID_26897342,Human_RBP_ID_27154463,Human_RBP_ID_27207175 Human_Splice_Rec_1278690,Human_Splice_Rec_1278691,Human_Splice_Rec_1278698,Human_Splice_Rec_1278699,Human_Splice_Rec_1278706,Human_Splice_Rec_1278707,Human_Splice_Rec_1278718,Human_Splice_Rec_1278719,Human_Splice_Rec_1278724,Human_Splice_Rec_1278725,Human_Splice_Rec_1278746,Human_Splice_Rec_1278747,Human_Splice_Rec_1278758,Human_Splice_Rec_1278759,Human_Splice_Rec_1278768,Human_Splice_Rec_1278769,Human_Splice_Rec_1278778,Human_Splice_Rec_1278779,Human_Splice_Rec_1278790,Human_Splice_Rec_1278791,Human_Splice_Rec_1278800,Human_Splice_Rec_1278801,Human_Splice_Rec_1278808,Human_Splice_Rec_1278809,Human_Splice_Rec_1278818,Human_Splice_Rec_1278819,Human_Splice_Rec_1278830,Human_Splice_Rec_1278831,Human_Splice_Rec_1278838,Human_Splice_Rec_1278839,Human_Splice_Rec_1278842,Human_Splice_Rec_1278843,Human_Splice_Rec_1278849,Human_Splice_Rec_1278853,Human_Splice_Rec_1278859 Human_miRNA_ID_2825135,Human_miRNA_ID_2859104 RMVar_hsa_circ_17802,RMVar_hsa_circ_1922,RMVar_hsa_circ_125894,RMVar_hsa_circ_334233,RMVar_hsa_circ_98159,RMVar_hsa_circ_151784,RMVar_hsa_circ_151785,RMVar_hsa_circ_83516,RMVar_hsa_circ_151786 78496 RMVar_ID_78496 Human_SNP_ID_472634220 m1A Human chr11 - 75400815 75400815 75400815 ATGGCCAGTCAAATGAGTTTTACCTGGTGGCTAAGATAATGATTTCTGTCCTGGTTGGTGTAACT ATGGCCAGTCAAATGAGTTTTACCTGGTGGCTTAGATAATGATTTCTGTCCTGGTTGGTGTAACT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:75400801..75400825 26863196 MeRIP-seq:(Medium) rs3206671 Functional Loss SNV dbSNP153 33..33 33 - - - 78497 RMVar_ID_78497 Human_SNP_ID_472634501 m1A Human chr11 + 75401718 75401718 75401718 ACTGCTGTAGTTCAGAAGAGGTTTGGCTTTCCAGAGGGCAGTGTAGAGGTGAGTGATTCTGGCAT ACTGCTGTAGTTCAGAAGAGGTTTGGCTTTCCGGAGGGCAGTGTAGAGGTGAGTGATTCTGGCAT A G RPS3 Ensembl:ENSG00000149273 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:75401609..75401787;chr11:75401651..75401725;chr11:75401626..75401750 26863196 MeRIP-seq:(Medium) rs369448212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403778,Human_RBP_ID_749808,Human_RBP_ID_869290,Human_RBP_ID_1460306,Human_RBP_ID_1782620,Human_RBP_ID_2284039,Human_RBP_ID_3380219,Human_RBP_ID_8358988,Human_RBP_ID_9006381,Human_RBP_ID_11716215,Human_RBP_ID_17649242,Human_RBP_ID_18612983,Human_RBP_ID_19050313,Human_RBP_ID_22532305,Human_RBP_ID_23207040,Human_RBP_ID_23521411 Human_Splice_Rec_1278692,Human_Splice_Rec_1278700,Human_Splice_Rec_1278701,Human_Splice_Rec_1278708,Human_Splice_Rec_1278709,Human_Splice_Rec_1278720,Human_Splice_Rec_1278721,Human_Splice_Rec_1278726,Human_Splice_Rec_1278727,Human_Splice_Rec_1278736,Human_Splice_Rec_1278737,Human_Splice_Rec_1278748,Human_Splice_Rec_1278749,Human_Splice_Rec_1278760,Human_Splice_Rec_1278761,Human_Splice_Rec_1278770,Human_Splice_Rec_1278771,Human_Splice_Rec_1278780,Human_Splice_Rec_1278781,Human_Splice_Rec_1278792,Human_Splice_Rec_1278793,Human_Splice_Rec_1278802,Human_Splice_Rec_1278810,Human_Splice_Rec_1278811,Human_Splice_Rec_1278820,Human_Splice_Rec_1278821,Human_Splice_Rec_1278832,Human_Splice_Rec_1278833,Human_Splice_Rec_1278840,Human_Splice_Rec_1278844,Human_Splice_Rec_1278845,Human_Splice_Rec_1278860,Human_Splice_Rec_1278861 RMVar_hsa_circ_17802,RMVar_hsa_circ_125894,RMVar_hsa_circ_334233,RMVar_hsa_circ_98159,RMVar_hsa_circ_151784,RMVar_hsa_circ_151785,RMVar_hsa_circ_83516,RMVar_hsa_circ_76149,RMVar_hsa_circ_84769,RMVar_hsa_circ_151786,RMVar_hsa_circ_151787,RMVar_hsa_circ_151788 78498 RMVar_ID_78498 Human_SNP_ID_472635362 m1A Human chr11 - 75404763 75404763 75404763 GTGGTGGGCAGTATCTCATCTTTGGGTTCCACAATGCTCACGTGGTCAGGCAGGGGCTTCTTAGG GTGGTGGGCAGTATCTCATCTTTGGGTTCCACGATGCTCACGTGGTCAGGCAGGGGCTTCTTAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:75404651..75404875;chr11:75403932..75404850 32194978 MeRIP-seq:(Medium) rs1278748349 Functional Loss SNV dbSNP153 33..33 33 - - - 78499 RMVar_ID_78499 Human_SNP_ID_472635374 m1A Human chr11 - 75404801 75404801 75404801 GCGGCTCTGGCTTCCCACCCTTCTGTTCTGAGATGGGGGTGGTGGGCAGTATCTCATCTTTGGGT GCGGCTCTGGCTTCCCACCCTTCTGTTCTGAGGTGGGGGTGGTGGGCAGTATCTCATCTTTGGGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:75404751..75404875 26863196 MeRIP-seq:(Medium) rs759369058 Functional Loss SNV dbSNP153 33..33 33 - - - 78500 RMVar_ID_78500 Human_SNP_ID_472635633 m1A Human chr11 - 75405643 75405643 75405643 ATTTTATTAAAGGTCTTTAGAGAGCAACATCCAGACTCCAGAATACAGCTGCCAAGGAGACCCTG ATTTTATTAAAGGTCTTTAGAGAGCAACATCCGGACTCCAGAATACAGCTGCCAAGGAGACCCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75405626..75405700 26863196 MeRIP-seq:(Medium) rs1445247545 Functional Loss SNV dbSNP153 33..33 33 - - - 78501 RMVar_ID_78501 Human_SNP_ID_472641263 m1A Human chr11 - 75425481 75425475 75425482 CAACACCTGGGCGGCCGCCGCGCCCCTCCCGGAGGCCGTGAGCTCGGCGGCGGTGGCGTCCTGCG CAACACCTGGGCGGCCGCCGCGCCCCTCCCG_______TGAGCTCGGCGGCGGTGGCGTCCTGCG ACGGCCTC A KLHL35 Ensembl:ENSG00000149243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75425433..75425584 26863196 MeRIP-seq:(Medium) rs779936640 Functional Loss DEL dbSNP153 32..38 33 - - - Human_Splice_Rec_1278873,Human_Splice_Rec_1278883,Human_Splice_Rec_1278891 78502 RMVar_ID_78502 Human_SNP_ID_472642853 m1A Human chr11 + 75430130 75430130 75430130 GGACGCGGCCGCAGCGCTCGGCCAGCGGGGCCAGCGAGAAGGCGGCGGCCACGCGGCGCAGCGCT GGACGCGGCCGCAGCGCTCGGCCAGCGGGGCCGGCGAGAAGGCGGCGGCCACGCGGCGCAGCGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75430079..75430180 26863196 MeRIP-seq:(Medium) rs1397914067 Functional Loss SNV dbSNP153 33..33 33 - - - 78503 RMVar_ID_78503 Human_SNP_ID_472642854 m1A Human chr11 + 75430130 75430130 75430130 GGACGCGGCCGCAGCGCTCGGCCAGCGGGGCCAGCGAGAAGGCGGCGGCCACGCGGCGCAGCGCT GGACGCGGCCGCAGCGCTCGGCCAGCGGGGCCTGCGAGAAGGCGGCGGCCACGCGGCGCAGCGCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75430079..75430180 26863196 MeRIP-seq:(Medium) rs1397914067 Functional Loss SNV dbSNP153 33..33 33 - - - 78504 RMVar_ID_78504 Human_SNP_ID_472642979 m1A Human chr11 + 75430322 75430321 75430322 CCGCTCCGTACACGTAGTCGAGCACCACGGCCAGCGCCGCCGCCGCCCCGGCCGGGCTCGTGCCT CCGCTCCGTACACGTAGTCGAGCACCACGGCC_GCGCCGCCGCCGCCCCGGCCGGGCTCGTGCCT CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75430271..75430399 26863196 MeRIP-seq:(Medium) rs1364457063 Functional Loss DEL dbSNP153 33..33 33 - - - 78505 RMVar_ID_78505 Human_SNP_ID_472642980 m1A Human chr11 + 75430322 75430322 75430322 CCGCTCCGTACACGTAGTCGAGCACCACGGCCAGCGCCGCCGCCGCCCCGGCCGGGCTCGTGCCT CCGCTCCGTACACGTAGTCGAGCACCACGGCCGGCGCCGCCGCCGCCCCGGCCGGGCTCGTGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75430271..75430399 26863196 MeRIP-seq:(Medium) rs1000842286 Functional Loss SNV dbSNP153 33..33 33 - - - 78506 RMVar_ID_78506 Human_SNP_ID_472644365 m1A Human chr11 + 75435276 75435276 75435276 GGGGACCAAGCCCTAGGCCCCATACTTCCCAGAAGGAGCCCCAGGCCTGCAGGGGCATCTGAAAG GGGGACCAAGCCCTAGGCCCCATACTTCCCAGCAGGAGCCCCAGGCCTGCAGGGGCATCTGAAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:75435237..75435487 32194978 MeRIP-seq:(Medium) rs1335761715 Functional Loss SNV dbSNP153 33..33 33 - - - 78507 RMVar_ID_78507 Human_SNP_ID_472649768 m1A Human chr11 + 75455417 75455417 75455417 GGGGGGACCAGGGGCTGCTCACGGCTCCTACCACTCTAAGACTTCAGTCTCTGGGGTCTGACTCC GGGGGGACCAGGGGCTGCTCACGGCTCCTACCCCTCTAAGACTTCAGTCTCTGGGGTCTGACTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75455414..75455513 26863196 MeRIP-seq:(Medium) rs960370279 Functional Loss SNV dbSNP153 33..33 33 - - - 78508 RMVar_ID_78508 Human_SNP_ID_472650036 m1A Human chr11 - 75456659 75456659 75456659 AGGGCCTGGCCACCATGTCCCTCCCCTGGATCACCGTTAGAATTGTTCTCATAGCTAAGGCTGAG AGGGCCTGGCCACCATGTCCCTCCCCTGGATCGCCGTTAGAATTGTTCTCATAGCTAAGGCTGAG T C GDPD5 Ensembl:ENSG00000158555 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75456656..75456727 26863196 MeRIP-seq:(Medium) rs1793410 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9364,GWAS_ID_9365,GWAS_ID_9366,GWAS_ID_9367,GWAS_ID_9368,GWAS_ID_9369,GWAS_ID_9370,GWAS_ID_9371,GWAS_ID_9372,GWAS_ID_9373,GWAS_ID_9374,GWAS_ID_9375,GWAS_ID_9376,GWAS_ID_9377,GWAS_ID_9378 RMVar_hsa_circ_110753,RMVar_hsa_circ_151799,RMVar_hsa_circ_349533,RMVar_hsa_circ_151800 78509 RMVar_ID_78509 Human_SNP_ID_472667629 m1A Human chr11 + 75531558 75531558 75531558 CCATTGGGACTGTGGGTGACTTGGGAAGGGTGATGTGCATAGGGTGGGAGGCAGGAGCAGGGGCT CCATTGGGACTGTGGGTGACTTGGGAAGGGTGTTGTGCATAGGGTGGGAGGCAGGAGCAGGGGCT A T lnc-SERPINH1-3,lnc-SERPINH1-3:2,lnc-SERPINH1-3:3 RNACentral:URS0000D59BE3,RNACentral:URS0000D56DA8,RNACentral:URS0000D5898B lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:75531446..75531585 26863196 MeRIP-seq:(Medium) rs1185030039 Functional Loss SNV dbSNP153 33..33 33 - - - 78510 RMVar_ID_78510 Human_SNP_ID_472674940 m1A Human chr11 + 75562308 75562307 75562309 CGAGAGCGAGAGTCACGTCCCGGCGCTAGCCCAGCCCGACCCAGGTGAGGGGCGGGAGACGCCTG CGAGAGCGAGAGTCACGTCCCGGCGCTAGCCC__CCCGACCCAGGTGAGGGGCGGGAGACGCCTG CAG C SERPINH1 Ensembl:ENSG00000149257 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75562154..75562369 26863196 MeRIP-seq:(Medium) rs1286456655 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_227725,Human_RBP_ID_1460398,Human_RBP_ID_4185286,Human_RBP_ID_5461189,Human_RBP_ID_22433876 Human_Splice_Rec_1279157,Human_Splice_Rec_1279167,Human_Splice_Rec_1279169,Human_Splice_Rec_1279179,Human_Splice_Rec_1279185,Human_Splice_Rec_1279187,Human_Splice_Rec_1279189,Human_Splice_Rec_1279197,Human_Splice_Rec_1279205 78511 RMVar_ID_78511 Human_SNP_ID_472676846 m1A Human chr11 + 75569035 75569035 75569035 CAAGCTCTCCAGCCTCATCATCCTCATGCCCCATCACGTGGAGCCTCTCGAGCGCCTTGAAAAGC CAAGCTCTCCAGCCTCATCATCCTCATGCCCCTTCACGTGGAGCCTCTCGAGCGCCTTGAAAAGC A T SERPINH1 Ensembl:ENSG00000149257 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75568984..75569062 26863196 MeRIP-seq:(Medium) rs267603192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_403855,Human_RBP_ID_4178887,Human_RBP_ID_22753756,Human_RBP_ID_26897392 Human_Splice_Rec_1279164,Human_Splice_Rec_1279176,Human_Splice_Rec_1279184,Human_Splice_Rec_1279196,Human_Splice_Rec_1279202,Human_Splice_Rec_1279212,Human_Splice_Rec_1279218,Human_Splice_Rec_1279234,Human_Splice_Rec_1279240 Human_miRNA_ID_1394320 RMVar_hsa_circ_23681,RMVar_hsa_circ_119542,RMVar_hsa_circ_151805,RMVar_hsa_circ_151807,RMVar_hsa_circ_331095 78512 RMVar_ID_78512 Human_SNP_ID_472676890 m1A Human chr11 + 75569127 75569127 75569127 GGATGGGGAAGATGCAGAAGAAGGCTGTTGCCATCTCCTTGCCCAAGGGTGTGGTGGAGGTGACC GGATGGGGAAGATGCAGAAGAAGGCTGTTGCCGTCTCCTTGCCCAAGGGTGTGGTGGAGGTGACC A G SERPINH1 Ensembl:ENSG00000149257 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:75569076..75569175 32194978 MeRIP-seq:(Medium) rs747059624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30770,Human_RBP_ID_403857,Human_RBP_ID_870195,Human_RBP_ID_5110600,Human_RBP_ID_6095341,Human_RBP_ID_9322318,Human_RBP_ID_18469031,Human_RBP_ID_19695910,Human_RBP_ID_22034833,Human_RBP_ID_22433885,Human_RBP_ID_22753758,Human_RBP_ID_27207211 Human_Splice_Rec_1279165,Human_Splice_Rec_1279203,Human_Splice_Rec_1279219,Human_Splice_Rec_1279241 Human_miRNA_ID_2621123 RMVar_hsa_circ_23681,RMVar_hsa_circ_119542,RMVar_hsa_circ_151805,RMVar_hsa_circ_151807,RMVar_hsa_circ_331095 78513 RMVar_ID_78513 Human_SNP_ID_472677659 m1A Human chr11 + 75571947 75571947 75571947 CAACCCCTTTGACCAGGACATCTACGGGCGCGAGGAGCTGCGCAGCCCCAAGCTGTTCTACGCCG CAACCCCTTTGACCAGGACATCTACGGGCGCGCGGAGCTGCGCAGCCCCAAGCTGTTCTACGCCG A C SERPINH1 Ensembl:ENSG00000149257 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:75571896..75572245 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_752345,Human_RBP_ID_18188378,Human_RBP_ID_22433208,Human_RBP_ID_22753764 78514 RMVar_ID_78514 Human_SNP_ID_472677663 m1A Human chr11 + 75571950 75571950 75571950 CCCCTTTGACCAGGACATCTACGGGCGCGAGGAGCTGCGCAGCCCCAAGCTGTTCTACGCCGACC CCCCTTTGACCAGGACATCTACGGGCGCGAGGTGCTGCGCAGCCCCAAGCTGTTCTACGCCGACC A T SERPINH1 Ensembl:ENSG00000149257 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:75571901..75572237 32194978 MeRIP-seq:(Medium) rs545800102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752345,Human_RBP_ID_18188378,Human_RBP_ID_22433208,Human_RBP_ID_22753764 78515 RMVar_ID_78515 Human_SNP_ID_472677682 m1A Human chr11 - 75571988 75571987 75571988 GCCGCTTTGGGTGTCCCGCACTAGGAAGATGAAGGGGTGGTCGGCGTAGAACAGCTTGGGGCTGC GCCGCTTTGGGTGTCCCGCACTAGGAAGATGA_GGGGTGGTCGGCGTAGAACAGCTTGGGGCTGC CT C lnc-MAP6-1,lnc-MAP6-1:2 RNACentral:URS00008C3F65,RNACentral:URS00009AD94C lincRNA,lincRNA exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:75571946..75572125 26863196 MeRIP-seq:(Medium) rs780318381 Functional Loss DEL dbSNP153 33..33 33 - - - 78516 RMVar_ID_78516 Human_SNP_ID_472677699 m1A Human chr11 - 75572025 75572025 75572025 CCTTAGGCCGGACCAGGCGCCCAATGAATAGCAGGGAGCCGCTTTGGGTGTCCCGCACTAGGAAG CCTTAGGCCGGACCAGGCGCCCAATGAATAGCTGGGAGCCGCTTTGGGTGTCCCGCACTAGGAAG T A lnc-MAP6-1,lnc-MAP6-1:2 RNACentral:URS00008C3F65,RNACentral:URS00009AD94C lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:75572001..75572025 26863196 MeRIP-seq:(Medium) rs943602399 Functional Loss SNV dbSNP153 33..33 33 - - - 78517 RMVar_ID_78517 Human_SNP_ID_472677700 m1A Human chr11 - 75572025 75572025 75572025 CCTTAGGCCGGACCAGGCGCCCAATGAATAGCAGGGAGCCGCTTTGGGTGTCCCGCACTAGGAAG CCTTAGGCCGGACCAGGCGCCCAATGAATAGCGGGGAGCCGCTTTGGGTGTCCCGCACTAGGAAG T C lnc-MAP6-1,lnc-MAP6-1:2 RNACentral:URS00008C3F65,RNACentral:URS00009AD94C lincRNA,lincRNA exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:75572001..75572025 26863196 MeRIP-seq:(Medium) rs943602399 Functional Loss SNV dbSNP153 33..33 33 - - - 78518 RMVar_ID_78518 Human_SNP_ID_472734566 m1A Human chr11 + 75815260 75815260 75815260 TAGCCAGCGGCGGCAACGGCGGCAGCGGCGGCAGCGGCGGCGGCTACTGTCTGGGCTGAGCAGTA TAGCCAGCGGCGGCAACGGCGGCAGCGGCGGCGGCGGCGGCGGCTACTGTCTGGGCTGAGCAGTA A G UVRAG Ensembl:ENSG00000198382 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:75815214..75815301 26863196 MeRIP-seq:(Medium) rs958653979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9321739 78519 RMVar_ID_78519 Human_SNP_ID_472734567 m1A Human chr11 + 75815260 75815260 75815260 TAGCCAGCGGCGGCAACGGCGGCAGCGGCGGCAGCGGCGGCGGCTACTGTCTGGGCTGAGCAGTA TAGCCAGCGGCGGCAACGGCGGCAGCGGCGGCTGCGGCGGCGGCTACTGTCTGGGCTGAGCAGTA A T UVRAG Ensembl:ENSG00000198382 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:75815214..75815301 26863196 MeRIP-seq:(Medium) rs958653979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9321739 78520 RMVar_ID_78520 Human_SNP_ID_472734577 m1A Human chr11 - 75815272 75815272 75815272 CCCGAGAGGCACTACTGCTCAGCCCAGACAGTAGCCGCCGCCGCTGCCGCCGCTGCCGCCGTTGC CCCGAGAGGCACTACTGCTCAGCCCAGACAGTTGCCGCCGCCGCTGCCGCCGCTGCCGCCGTTGC T A UVRAG-DT Ensembl:ENSG00000255507 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75815221..75815417 26863196 MeRIP-seq:(Medium) rs915108783 Functional Loss SNV dbSNP153 33..33 33 - - - 78521 RMVar_ID_78521 Human_SNP_ID_472734578 m1A Human chr11 - 75815272 75815272 75815272 CCCGAGAGGCACTACTGCTCAGCCCAGACAGTAGCCGCCGCCGCTGCCGCCGCTGCCGCCGTTGC CCCGAGAGGCACTACTGCTCAGCCCAGACAGTGGCCGCCGCCGCTGCCGCCGCTGCCGCCGTTGC T C UVRAG-DT Ensembl:ENSG00000255507 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75815221..75815417 26863196 MeRIP-seq:(Medium) rs915108783 Functional Loss SNV dbSNP153 33..33 33 - - - 78522 RMVar_ID_78522 Human_SNP_ID_472781469 m1A Human chr11 + 76010831 76010831 76010831 TGGAGCATAGTGAGCGAGGGAAGAGCTACGTTAGAAGAGGTAGGAGAGGGCAGCCAGGGCCTTGA TGGAGCATAGTGAGCGAGGGAAGAGCTACGTTGGAAGAGGTAGGAGAGGGCAGCCAGGGCCTTGA A G UVRAG Ensembl:ENSG00000198382 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:76010794..76010877 26863196 MeRIP-seq:(Medium) rs1010173959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358357,RMVar_hsa_circ_32211,RMVar_hsa_circ_29678,RMVar_hsa_circ_316260,RMVar_hsa_circ_151822,RMVar_hsa_circ_291493,RMVar_hsa_circ_55686,RMVar_hsa_circ_151825,RMVar_hsa_circ_59685,RMVar_hsa_circ_280192,RMVar_hsa_circ_151827,RMVar_hsa_circ_151826,RMVar_hsa_circ_291961 78523 RMVar_ID_78523 Human_SNP_ID_472872807 m1A Human chr11 + 76380920 76380920 76380920 CAGTCCGCCCGCCCGTCGGGGCCGGGGAGGGGAGCCAGGCCGGCCGGCCGGCTCGGCAGGGCCGA CAGTCCGCCCGCCCGTCGGGGCCGGGGAGGGGTGCCAGGCCGGCCGGCCGGCTCGGCAGGGCCGA A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:76380820..76380923 26863410 MeRIP-seq:(Medium) rs1200965823 Functional Loss SNV dbSNP153 33..33 33 - - - 78524 RMVar_ID_78524 Human_SNP_ID_472887167 m1A Human chr11 - 76444609 76444609 76444609 GGCTCTGCTGCGACCTTTACGGTAGTGAGGTTAGGGACGATGGGAGAGCAGCTTTGTTCCTGAAG GGCTCTGCTGCGACCTTTACGGTAGTGAGGTTGGGGACGATGGGAGAGCAGCTTTGTTCCTGAAG T C AP002360.2 Ensembl:ENSG00000255135 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:76444558..76444656 26863196 MeRIP-seq:(Medium) rs556972602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4179132,Human_RBP_ID_5093611,Human_RBP_ID_11719539 78525 RMVar_ID_78525 Human_SNP_ID_472974599 m1A Human chr11 - 76795708 76795708 76795708 CCCGAGTCAGGCTGAAGCTGTCGAAAAGGCCGAAGGTCTCCACCTCGCATTGGCACCCGGGGAAG CCCGAGTCAGGCTGAAGCTGTCGAAAAGGCCGCAGGTCTCCACCTCGCATTGGCACCCGGGGAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:76795659..76795817 26863196 MeRIP-seq:(Medium) rs1293338522 Functional Loss SNV dbSNP153 33..33 33 - - - 78526 RMVar_ID_78526 Human_SNP_ID_472974669 m1A Human chr11 - 76795900 76795900 76795900 GGGAGAAGGCAGTGGGTGAGATGCTGGTGAGCAGGTTGTGGCTGAGATCCAGGCCAGCCAACGTC GGGAGAAGGCAGTGGGTGAGATGCTGGTGAGCGGGTTGTGGCTGAGATCCAGGCCAGCCAACGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:76795850..76795943 26863196 MeRIP-seq:(Medium) rs746610558 Functional Loss SNV dbSNP153 33..33 33 - - - 78527 RMVar_ID_78527 Human_SNP_ID_472974819 m1A Human chr11 + 76796225 76796225 76796225 TGGAACCGGCTCCATGCCGTGCCCAACCTCCGAGACTTGCCCCTGCGCTACCTGAGCCTGGATGG TGGAACCGGCTCCATGCCGTGCCCAACCTCCGTGACTTGCCCCTGCGCTACCTGAGCCTGGATGG A T TSKU Ensembl:ENSG00000182704 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:76795916..76796284 26863196 MeRIP-seq:(Medium) rs1264617963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5110605,Human_RBP_ID_27416326 RMVar_hsa_circ_100357,RMVar_hsa_circ_151860 78528 RMVar_ID_78528 Human_SNP_ID_472975187 m1A Human chr11 + 76797355 76797355 76797355 GGACCCAATGCACTTTCTTGTCTCCTCTAATAAGCCCCACCCTCCCCGCCTGGGCTCCCCTTGCT GGACCCAATGCACTTTCTTGTCTCCTCTAATATGCCCCACCCTCCCCGCCTGGGCTCCCCTTGCT A T TSKU Ensembl:ENSG00000182704 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:76797307..76797408 32194978 MeRIP-seq:(Medium) rs1399738726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404053,Human_RBP_ID_2285264,Human_RBP_ID_18933898,Human_RBP_ID_27416356 Human_miRNA_ID_2146747,Human_miRNA_ID_2988172,Human_miRNA_ID_3021872 RMVar_hsa_circ_100357,RMVar_hsa_circ_151860 78529 RMVar_ID_78529 Human_SNP_ID_472975251 m1A Human chr11 + 76797557 76797557 76797557 GGGCACATTGGTTCCAGCCTAGCCAGTTTCTCACCCTGGGTTGGGGTCCCCCAGCATCCAGACTG GGGCACATTGGTTCCAGCCTAGCCAGTTTCTCGCCCTGGGTTGGGGTCCCCCAGCATCCAGACTG A G TSKU Ensembl:ENSG00000182704 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:76797506..76797706 32194978 MeRIP-seq:(Medium) rs1238555485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8176024,Human_RBP_ID_8359360,Human_RBP_ID_17074246,Human_RBP_ID_18932843 Human_miRNA_ID_1792020 RMVar_hsa_circ_100357,RMVar_hsa_circ_151860 78530 RMVar_ID_78530 Human_SNP_ID_472991994 m1A Human chr11 + 76861094 76861094 76861094 GGTACATCGCCGAGTTCTGTGAGTGTGGCCTGAGGAGGGGAGTGGGGGCGAGAGGGCACCGGGCT GGTACATCGCCGAGTTCTGTGAGTGTGGCCTGCGGAGGGGAGTGGGGGCGAGAGGGCACCGGGCT A C ACER3 Ensembl:ENSG00000078124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:76861093..76861178 26863196 MeRIP-seq:(Medium) rs1565145898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89738,RMVar_hsa_circ_151861 78531 RMVar_ID_78531 Human_SNP_ID_473070839 m1A Human chr11 - 77181991 77181991 77181991 CATCCTCGTCAGGCAGGGGCAGGGCTGCATCCAGGTCCTCCTCCACCATCTCCCTCCGCCCTCGC CATCCTCGTCAGGCAGGGGCAGGGCTGCATCCGGGTCCTCCTCCACCATCTCCCTCCGCCCTCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:77181921..77182004 26863196 MeRIP-seq:(Medium) rs1197258252 Functional Loss SNV dbSNP153 33..33 33 - - - 78532 RMVar_ID_78532 Human_SNP_ID_473074358 m1A Human chr11 - 77193347 77193347 77193347 CCAACAACACTGTCATTGTCAACACCACCATCACTACCTTTACCATCACCACTATCATCACTACC CCAACAACACTGTCATTGTCAACACCACCATCGCTACCTTTACCATCACCACTATCATCACTACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:77193327..77193459 26863196 MeRIP-seq:(Medium) rs997657754 Functional Loss SNV dbSNP153 33..33 33 - - - 78533 RMVar_ID_78533 Human_SNP_ID_473112463 m1A Human chr11 - 77339502 77339499 77339503 TTAATACCAGGCTGGGATTCTTAGGGGTTCTGACTTTTTTTTTTGTTCCACTACTAATGCAGTAT TTAATACCAGGCTGGGATTCTTAGGGGTTCT____TTTTTTTTTGTTCCACTACTAATGCAGTAT AAGTC A PAK1 Ensembl:ENSG00000149269 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:77339414..77339503 26863410 MeRIP-seq:(Medium) rs1323191243 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_10105,RMVar_hsa_circ_151878,RMVar_hsa_circ_80583,RMVar_hsa_circ_296024,RMVar_hsa_circ_300105,RMVar_hsa_circ_321147,RMVar_hsa_circ_319744,RMVar_hsa_circ_296574,RMVar_hsa_circ_291428,RMVar_hsa_circ_26103,RMVar_hsa_circ_151880,RMVar_hsa_circ_151882,RMVar_hsa_circ_151884,RMVar_hsa_circ_151885,RMVar_hsa_circ_151883,RMVar_hsa_circ_151881,RMVar_hsa_circ_96052,RMVar_hsa_circ_373317,RMVar_hsa_circ_151889,RMVar_hsa_circ_126302,RMVar_hsa_circ_151886,RMVar_hsa_circ_151887,RMVar_hsa_circ_116738,RMVar_hsa_circ_151888 78534 RMVar_ID_78534 Human_SNP_ID_473143448 m1A Human chr11 - 77474208 77474208 77474208 CCGGAGCCGCAGCCGCCGCCGCCGCGCCGGGGAGGGGGAGTGGGGGAGGGGGAGGGGGAGAAGGG CCGGAGCCGCAGCCGCCGCCGCCGCGCCGGGGGGGGGGAGTGGGGGAGGGGGAGGGGGAGAAGGG T C PAK1 Ensembl:ENSG00000149269 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:77474115..77474309 26863196 MeRIP-seq:(Medium) rs1393779126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269423,Human_RBP_ID_5255890,Human_RBP_ID_8359475,Human_RBP_ID_11722155,Human_RBP_ID_17801656,Human_RBP_ID_22491836 78535 RMVar_ID_78535 Human_SNP_ID_473176052 m1A Human chr11 - 77611961 77611961 77611961 GGGGGTCAAAGGATCACTGGAGATGGGGTCCTAGAGAGACTGAGCTGAAAAGGGGTCAGTGGTTA GGGGGTCAAAGGATCACTGGAGATGGGGTCCTGGAGAGACTGAGCTGAAAAGGGGTCAGTGGTTA T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:77611839..77612160 26863196 MeRIP-seq:(Medium) rs1386216960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6096956,Human_RBP_ID_11722896,Human_RBP_ID_23267815,Human_RBP_ID_23522362 RMVar_hsa_circ_151908 78536 RMVar_ID_78536 Human_SNP_ID_473178590 m1A Human chr11 - 77622672 77622672 77622672 ATTTAAACTTTAAAGTTTTCTGTTTGTTTAGAACAAGGACAGGGGGACATCCCTACATTTTACAC ATTTAAACTTTAAAGTTTTCTGTTTGTTTAGATCAAGGACAGGGGGACATCCCTACATTTTACAC T A CLNS1A Ensembl:ENSG00000074201 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:77622650..77622727 26863196 MeRIP-seq:(Medium) rs1466608317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870319,Human_RBP_ID_9362789,Human_RBP_ID_11723363,Human_RBP_ID_22895201,Human_RBP_ID_23207057,Human_RBP_ID_24542986,Human_RBP_ID_26319037,Human_RBP_ID_27207430,Human_RBP_ID_27803857 Human_Splice_Rec_1281316,Human_Splice_Rec_1281326,Human_Splice_Rec_1281350,Human_Splice_Rec_1281362,Human_Splice_Rec_1281374,Human_Splice_Rec_1281378,Human_Splice_Rec_1281380 Human_miRNA_ID_2444116 RMVar_hsa_circ_151910,RMVar_hsa_circ_127604,RMVar_hsa_circ_151908,RMVar_hsa_circ_123342,RMVar_hsa_circ_91256,RMVar_hsa_circ_94520,RMVar_hsa_circ_151912,RMVar_hsa_circ_151911,RMVar_hsa_circ_151918,RMVar_hsa_circ_280548,RMVar_hsa_circ_345318,RMVar_hsa_circ_151909,RMVar_hsa_circ_341566,RMVar_hsa_circ_271847,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_306901,RMVar_hsa_circ_151916,RMVar_hsa_circ_151917,RMVar_hsa_circ_376873,RMVar_hsa_circ_151921,RMVar_hsa_circ_289519,RMVar_hsa_circ_151920 78537 RMVar_ID_78537 Human_SNP_ID_473179178 m1A Human chr11 - 77625007 77625007 77625007 CCAGGCCTTGCATCCAGATCCTGAGGATGAGGATTCAGATGACTACGATGGAGAAGAATATGATG CCAGGCCTTGCATCCAGATCCTGAGGATGAGGGTTCAGATGACTACGATGGAGAAGAATATGATG T C CLNS1A Ensembl:ENSG00000074201 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:77622519..77625108 32194978 MeRIP-seq:(Medium) rs1368196862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29483,Human_RBP_ID_404216,Human_RBP_ID_1460517,Human_RBP_ID_1782820,Human_RBP_ID_3380662,Human_RBP_ID_4179513,Human_RBP_ID_6097081,Human_RBP_ID_8246574,Human_RBP_ID_9362790,Human_RBP_ID_11723470,Human_RBP_ID_18252512,Human_RBP_ID_18526384,Human_RBP_ID_23522401,Human_RBP_ID_26319038,Human_RBP_ID_27416399,Human_RBP_ID_27803858 Human_Splice_Rec_1281314,Human_Splice_Rec_1281315,Human_Splice_Rec_1281324,Human_Splice_Rec_1281325,Human_Splice_Rec_1281336,Human_Splice_Rec_1281337,Human_Splice_Rec_1281360,Human_Splice_Rec_1281361,Human_Splice_Rec_1281372,Human_Splice_Rec_1281373,Human_Splice_Rec_1281377,Human_Splice_Rec_1281379 RMVar_hsa_circ_151910,RMVar_hsa_circ_127604,RMVar_hsa_circ_151908,RMVar_hsa_circ_123342,RMVar_hsa_circ_94520,RMVar_hsa_circ_151911,RMVar_hsa_circ_85782,RMVar_hsa_circ_151918,RMVar_hsa_circ_280548,RMVar_hsa_circ_345318,RMVar_hsa_circ_151909,RMVar_hsa_circ_271847,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_306901,RMVar_hsa_circ_151917,RMVar_hsa_circ_376873,RMVar_hsa_circ_151921,RMVar_hsa_circ_289519,RMVar_hsa_circ_277322,RMVar_hsa_circ_151920,RMVar_hsa_circ_275228,RMVar_hsa_circ_151923,RMVar_hsa_circ_151924,RMVar_hsa_circ_151925,RMVar_hsa_circ_151922 78538 RMVar_ID_78538 Human_SNP_ID_473180480 m1A Human chr11 - 77629884 77629884 77629884 TAAAACATGTTTTTCAGCCGCCTGTCTTGGTTAGATGGCTCTGGATTAGGATTCTCACTGGAATA TAAAACATGTTTTTCAGCCGCCTGTCTTGGTTGGATGGCTCTGGATTAGGATTCTCACTGGAATA T C CLNS1A Ensembl:ENSG00000074201 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:77629834..77629946 26863196 MeRIP-seq:(Medium) rs748657979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1460530,Human_RBP_ID_1782825,Human_RBP_ID_4179530,Human_RBP_ID_6097105,Human_RBP_ID_11723583,Human_RBP_ID_18613271,Human_RBP_ID_22641930,Human_RBP_ID_26319040 Human_Splice_Rec_1281310,Human_Splice_Rec_1281322,Human_Splice_Rec_1281332,Human_Splice_Rec_1281348,Human_Splice_Rec_1281356 Human_miRNA_ID_1602930,Human_miRNA_ID_1677188,Human_miRNA_ID_2825139,Human_miRNA_ID_2859108 RMVar_hsa_circ_151910,RMVar_hsa_circ_151908,RMVar_hsa_circ_123342,RMVar_hsa_circ_94520,RMVar_hsa_circ_85782,RMVar_hsa_circ_151918,RMVar_hsa_circ_151909,RMVar_hsa_circ_271847,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_151921,RMVar_hsa_circ_289519,RMVar_hsa_circ_277322,RMVar_hsa_circ_122384,RMVar_hsa_circ_151923,RMVar_hsa_circ_151922,RMVar_hsa_circ_151926 78539 RMVar_ID_78539 Human_SNP_ID_473182547 m1A Human chr11 + 77637697 77637697 77637697 AGGAGCCCCTCCGCTGGCCCAGGCGGCGGGAAACTTTTGAGGAAGCTCATAGCAGCAGAGTGCGG AGGAGCCCCTCCGCTGGCCCAGGCGGCGGGAAGCTTTTGAGGAAGCTCATAGCAGCAGAGTGCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:77637554..77637775 26863410 MeRIP-seq:(Medium) rs1335936363 Functional Loss SNV dbSNP153 33..33 33 - - - 78540 RMVar_ID_78540 Human_SNP_ID_473182548 m1A Human chr11 - 77637699 77637698 77637699 TGCCGCACTCTGCTGCTATGAGCTTCCTCAAAAGTTTCCCGCCGCCTGGGCCAGCGGAGGGGCTC TGCCGCACTCTGCTGCTATGAGCTTCCTCAAA_GTTTCCCGCCGCCTGGGCCAGCGGAGGGGCTC CT C CLNS1A Ensembl:ENSG00000074201 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:77637626..77637700 32194978 MeRIP-seq:(Medium) rs1197923963 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_29489,Human_RBP_ID_404229,Human_RBP_ID_1460531,Human_RBP_ID_4179536,Human_RBP_ID_5460856,Human_RBP_ID_17801707,Human_RBP_ID_18613278,Human_RBP_ID_26897736 RMVar_hsa_circ_94520,RMVar_hsa_circ_85782,RMVar_hsa_circ_151909,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_151922 78541 RMVar_ID_78541 Human_SNP_ID_473204516 m1A Human chr11 - 77725496 77725496 77725496 TTTGTTTTGCTTTGTTTTGTAATCTCTTCCATATTCTTCCACTCCTCTTCCCAACTATATAATTC TTTGTTTTGCTTTGTTTTGTAATCTCTTCCATGTTCTTCCACTCCTCTTCCCAACTATATAATTC T C RSF1 Ensembl:ENSG00000048649 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:77725481..77725569 26863196 MeRIP-seq:(Medium) rs1407715131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3380718,Human_RBP_ID_5166808 RMVar_hsa_circ_109465,RMVar_hsa_circ_151936,RMVar_hsa_circ_269184,RMVar_hsa_circ_114467,RMVar_hsa_circ_108396,RMVar_hsa_circ_151945,RMVar_hsa_circ_151946,RMVar_hsa_circ_268557,RMVar_hsa_circ_378139,RMVar_hsa_circ_151947,RMVar_hsa_circ_46579,RMVar_hsa_circ_151957,RMVar_hsa_circ_151958,RMVar_hsa_circ_151959,RMVar_hsa_circ_151960 78542 RMVar_ID_78542 Human_SNP_ID_473226758 m1A Human chr11 - 77813676 77813676 77813676 GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTATGGCTTTGAAGGTTACCGGAAAAACACGCGTG GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTGTGGCTTTGAAGGTTACCGGAAAAACACGCGTG T C AP000580.1,RSF1 Ensembl:ENSG00000219529,Ensembl:ENSG00000048649 Pseudogene,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:77813636..77813705 26863196 MeRIP-seq:(Medium) rs58914857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404295,Human_RBP_ID_866844,Human_RBP_ID_1265958,Human_RBP_ID_9364192,Human_RBP_ID_19050338 Human_Splice_Rec_1281504 GWAS_ID_9379,GWAS_ID_9380,GWAS_ID_9381,GWAS_ID_9382,GWAS_ID_9383,GWAS_ID_9384,GWAS_ID_9385,GWAS_ID_9386,GWAS_ID_9387,GWAS_ID_9388,GWAS_ID_9389,GWAS_ID_9390,GWAS_ID_9391,GWAS_ID_9392,GWAS_ID_9393,GWAS_ID_9394,GWAS_ID_9395,GWAS_ID_9396,GWAS_ID_9397,GWAS_ID_9398,GWAS_ID_9399,GWAS_ID_9400,GWAS_ID_9401,GWAS_ID_9402,GWAS_ID_9403,GWAS_ID_9404,GWAS_ID_9405,GWAS_ID_9406,GWAS_ID_9407,GWAS_ID_9408,GWAS_ID_9409,GWAS_ID_9410,GWAS_ID_9411,GWAS_ID_9412,GWAS_ID_9413,GWAS_ID_9414,GWAS_ID_9415,GWAS_ID_9416,GWAS_ID_9417,GWAS_ID_9418,GWAS_ID_9419,GWAS_ID_9420,GWAS_ID_9421,GWAS_ID_9422,GWAS_ID_9423,GWAS_ID_9424,GWAS_ID_9425,GWAS_ID_9426,GWAS_ID_9427,GWAS_ID_9428,GWAS_ID_9429,GWAS_ID_9430,GWAS_ID_9431,GWAS_ID_9432,GWAS_ID_9433,GWAS_ID_9434,GWAS_ID_9435,GWAS_ID_9436,GWAS_ID_9437,GWAS_ID_9438 78543 RMVar_ID_78543 Human_SNP_ID_473226759 m1A Human chr11 - 77813676 77813676 77813676 GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTATGGCTTTGAAGGTTACCGGAAAAACACGCGTG GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTCTGGCTTTGAAGGTTACCGGAAAAACACGCGTG T G AP000580.1,RSF1 Ensembl:ENSG00000219529,Ensembl:ENSG00000048649 Pseudogene,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:77813636..77813705 26863196 MeRIP-seq:(Medium) rs58914857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404295,Human_RBP_ID_866844,Human_RBP_ID_1265958,Human_RBP_ID_9364192,Human_RBP_ID_19050338 Human_Splice_Rec_1281504 GWAS_ID_9379,GWAS_ID_9380,GWAS_ID_9381,GWAS_ID_9382,GWAS_ID_9383,GWAS_ID_9384,GWAS_ID_9385,GWAS_ID_9386,GWAS_ID_9387,GWAS_ID_9388,GWAS_ID_9389,GWAS_ID_9390,GWAS_ID_9391,GWAS_ID_9392,GWAS_ID_9393,GWAS_ID_9394,GWAS_ID_9395,GWAS_ID_9396,GWAS_ID_9397,GWAS_ID_9398,GWAS_ID_9399,GWAS_ID_9400,GWAS_ID_9401,GWAS_ID_9402,GWAS_ID_9403,GWAS_ID_9404,GWAS_ID_9405,GWAS_ID_9406,GWAS_ID_9407,GWAS_ID_9408,GWAS_ID_9409,GWAS_ID_9410,GWAS_ID_9411,GWAS_ID_9412,GWAS_ID_9413,GWAS_ID_9414,GWAS_ID_9415,GWAS_ID_9416,GWAS_ID_9417,GWAS_ID_9418,GWAS_ID_9419,GWAS_ID_9420,GWAS_ID_9421,GWAS_ID_9422,GWAS_ID_9423,GWAS_ID_9424,GWAS_ID_9425,GWAS_ID_9426,GWAS_ID_9427,GWAS_ID_9428,GWAS_ID_9429,GWAS_ID_9430,GWAS_ID_9431,GWAS_ID_9432,GWAS_ID_9433,GWAS_ID_9434,GWAS_ID_9435,GWAS_ID_9436,GWAS_ID_9437,GWAS_ID_9438 78544 RMVar_ID_78544 Human_SNP_ID_473228640 m1A Human chr11 + 77820580 77820580 77820580 GGCGGCGGCGCCTGCAGCACCCGCTCCAGCTCAGGGAACGGCAACTCAGGCAGGTCTAGCAGCGG GGCGGCGGCGCCTGCAGCACCCGCTCCAGCTCGGGGAACGGCAACTCAGGCAGGTCTAGCAGCGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:77820502..77820720 26863196 MeRIP-seq:(Medium) rs892592746 Functional Loss SNV dbSNP153 33..33 33 - - - 78545 RMVar_ID_78545 Human_SNP_ID_473228938 m1A Human chr11 - 77821209 77821209 77821209 CCACCGCACTGTCTCCTCAAAGTTGCGTTCCCAAACGGCGCAGTGCTCTGCCCGCACTTACGCTC CCACCGCACTGTCTCCTCAAAGTTGCGTTCCCGAACGGCGCAGTGCTCTGCCCGCACTTACGCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:77821158..77831958 26863196 MeRIP-seq:(Medium) rs1229961087 Functional Loss SNV dbSNP153 33..33 33 - - - 78546 RMVar_ID_78546 Human_SNP_ID_473233902 m1A Human chr11 - 77842502 77842502 77842502 TGCCCCCATGATAAGGAAGCAATTTCAGGGGAAGTCATAAGGAACTTCACTGAAGTCTGAAATTA TGCCCCCATGATAAGGAAGCAATTTCAGGGGACGTCATAAGGAACTTCACTGAAGTCTGAAATTA T G AP002812.2 Ensembl:ENSG00000254459 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:77842476..77855351 32194978 MeRIP-seq:(Medium) rs372498481 Functional Loss SNV dbSNP153 33..33 33 - - - 78547 RMVar_ID_78547 Human_SNP_ID_473240063 m1A Human chr11 + 77869723 77869723 77869723 GTACCTGTCTACTTTCTCTTTCCACATCCAGCATTCTCCTGGTGTGCAGCCTGCAGATGTGAAGG GTACCTGTCTACTTTCTCTTTCCACATCCAGCGTTCTCCTGGTGTGCAGCCTGCAGATGTGAAGG A G AAMDC Ensembl:ENSG00000087884 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:77869711..77872296 26863196 MeRIP-seq:(Medium) rs1465273976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4179690,Human_RBP_ID_23522657 Human_Splice_Rec_1281508,Human_Splice_Rec_1281509,Human_Splice_Rec_1281514,Human_Splice_Rec_1281515,Human_Splice_Rec_1281524,Human_Splice_Rec_1281525,Human_Splice_Rec_1281534,Human_Splice_Rec_1281535,Human_Splice_Rec_1281542,Human_Splice_Rec_1281543,Human_Splice_Rec_1281554,Human_Splice_Rec_1281555,Human_Splice_Rec_1281562,Human_Splice_Rec_1281563,Human_Splice_Rec_1281578,Human_Splice_Rec_1281579,Human_Splice_Rec_1281584,Human_Splice_Rec_1281585 RMVar_hsa_circ_114920,RMVar_hsa_circ_151967 78548 RMVar_ID_78548 Human_SNP_ID_473240096 m1A Human chr11 - 77869813 77869813 77869813 CAGGAATGCTGTGCATACCAACACCTACCTTCAAGGCCTCACTCATCCCTCGGCCAATCACAAGA CAGGAATGCTGTGCATACCAACACCTACCTTCGAGGCCTCACTCATCCCTCGGCCAATCACAAGA T C AP002812.2,AP002812.5 Ensembl:ENSG00000254459,Ensembl:ENSG00000255449 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:77869789..77872296 26863196 MeRIP-seq:(Medium) rs765873253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5550776 RMVar_hsa_circ_151968 78549 RMVar_ID_78549 Human_SNP_ID_473244062 m1A Human chr11 + 77886512 77886512 77886512 CTGAATGTCAAAGTGAAGAAATTCAATGAAGCACGGGTAAACGGCGGGAGTAACTATGACTCTCT CTGAATGTCAAAGTGAAGAAATTCAATGAAGCGCGGGTAAACGGCGGGAGTAACTATGACTCTCT A G AAMDC Ensembl:ENSG00000087884 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4542438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_110694,Human_RBP_ID_1080788,Human_RBP_ID_1163605,Human_RBP_ID_1460569,Human_RBP_ID_5255897,Human_RBP_ID_5416578,Human_RBP_ID_5436924,Human_RBP_ID_5461275,Human_RBP_ID_5490699,Human_RBP_ID_5550285,Human_RBP_ID_6097708,Human_RBP_ID_8246576,Human_RBP_ID_8359664,Human_RBP_ID_8772071,Human_RBP_ID_9006616,Human_RBP_ID_11725725,Human_RBP_ID_16988122,Human_RBP_ID_17233203,Human_RBP_ID_17349462,Human_RBP_ID_17466253,Human_RBP_ID_17806500,Human_RBP_ID_18252560,Human_RBP_ID_18510787,Human_RBP_ID_18613365,Human_RBP_ID_21916163,Human_RBP_ID_22420766,Human_RBP_ID_23125008,Human_RBP_ID_23305283,Human_RBP_ID_26606131,Human_RBP_ID_26747718,Human_RBP_ID_26897812,Human_RBP_ID_27154471 78550 RMVar_ID_78550 Human_SNP_ID_473269110 m1A Human chr11 + 77991279 77991277 77991280 GATTTACTTGGTTTTGTTAGTCGGAGTTTCTTAGTAGCAATTTCCTCCTGTGGCTGCAAGGGGTA GATTTACTTGGTTTTGTTAGTCGGAGTTTCT___TAGCAATTTCCTCCTGTGGCTGCAAGGGGTA TTAG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:77991256..77991327 26863196 MeRIP-seq:(Medium) rs756641747 Functional Loss DEL dbSNP153 32..34 33 - - - 78551 RMVar_ID_78551 Human_SNP_ID_473269954 m1A Human chr11 + 77994618 77994618 77994618 TTACCTGAACCACTTTCGTGAATTCCTCATAAACCCGCTTCTTAAGGTGCGCCGCCATGCCTACC TTACCTGAACCACTTTCGTGAATTCCTCATAAGCCCGCTTCTTAAGGTGCGCCGCCATGCCTACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:77994532..77994621 26863196 MeRIP-seq:(Medium) rs1216494552 Functional Loss SNV dbSNP153 33..33 33 - - - 78552 RMVar_ID_78552 Human_SNP_ID_473277079 m1A Human chr11 + 78022945 78022945 78022945 AAAGAGGAAAGGCTGGACAGAGCCAAACCAGAAAGGGACACCGAGGCGCGAAAGGAGAGTGATCC AAAGAGGAAAGGCTGGACAGAGCCAAACCAGACAGGGACACCGAGGCGCGAAAGGAGAGTGATCC A C AP003032.1 Ensembl:ENSG00000254675 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78022938..78023027 26863196 MeRIP-seq:(Medium) rs572696464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1281787 78553 RMVar_ID_78553 Human_SNP_ID_473277207 m1A Human chr11 + 78023218 78023218 78023218 GGGGCAGAGGGGTCTGGCTCGTCATCCTGCCCACTGGCCGCTCCACTGCGCAGCCCTGCCACATG GGGGCAGAGGGGTCTGGCTCGTCATCCTGCCCCCTGGCCGCTCCACTGCGCAGCCCTGCCACATG A C AP003032.1 Ensembl:ENSG00000254675 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:78017237..78023250 26863196 MeRIP-seq:(Medium) rs761063488 Functional Loss SNV dbSNP153 33..33 33 - - - 78554 RMVar_ID_78554 Human_SNP_ID_473277208 m1A Human chr11 + 78023218 78023218 78023218 GGGGCAGAGGGGTCTGGCTCGTCATCCTGCCCACTGGCCGCTCCACTGCGCAGCCCTGCCACATG GGGGCAGAGGGGTCTGGCTCGTCATCCTGCCCGCTGGCCGCTCCACTGCGCAGCCCTGCCACATG A G AP003032.1 Ensembl:ENSG00000254675 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:78017237..78023250 26863196 MeRIP-seq:(Medium) rs761063488 Functional Loss SNV dbSNP153 33..33 33 - - - 78555 RMVar_ID_78555 Human_SNP_ID_473291910 m1A Human chr11 - 78079607 78079607 78079609 TTGGGCTACTGCTCCGGCCTGATTGATAACCTAATCCGGCGGAGGCCGATCGCGACGGCTGGTGA TTGGGCTACTGCTCCGGCCTGATTGATAACGTGATCCGGCGGAGGCCGATCGCGACGGCTGGTGA TAG CAC NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs386755249 Functional Loss MNV dbSNP153 31..33 33 - - - Human_RBP_ID_751380,Human_RBP_ID_4184357,Human_RBP_ID_9276051,Human_RBP_ID_17682689,Human_RBP_ID_17804735,Human_RBP_ID_18974833,Human_RBP_ID_22433211,Human_RBP_ID_22753772,Human_RBP_ID_26410746,Human_RBP_ID_26804018 Human_Splice_Rec_1281771,Human_Splice_Rec_1281773,Human_Splice_Rec_1281777,Human_Splice_Rec_1281781,Human_Splice_Rec_1281791,Human_Splice_Rec_1281795,Human_Splice_Rec_1281799,Human_Splice_Rec_1281801,Human_Splice_Rec_1281805 78556 RMVar_ID_78556 Human_SNP_ID_473291911 m1A Human chr11 - 78079607 78079607 78079607 TTGGGCTACTGCTCCGGCCTGATTGATAACCTAATCCGGCGGAGGCCGATCGCGACGGCTGGTGA TTGGGCTACTGCTCCGGCCTGATTGATAACCTGATCCGGCGGAGGCCGATCGCGACGGCTGGTGA T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs534418 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_751380,Human_RBP_ID_4184357,Human_RBP_ID_9276051,Human_RBP_ID_17682689,Human_RBP_ID_17804735,Human_RBP_ID_18974833,Human_RBP_ID_22433211,Human_RBP_ID_22753772,Human_RBP_ID_26410746,Human_RBP_ID_26804018 Human_Splice_Rec_1281771,Human_Splice_Rec_1281773,Human_Splice_Rec_1281777,Human_Splice_Rec_1281781,Human_Splice_Rec_1281791,Human_Splice_Rec_1281795,Human_Splice_Rec_1281799,Human_Splice_Rec_1281801,Human_Splice_Rec_1281805 GWAS_ID_9439,GWAS_ID_9440,GWAS_ID_9441,GWAS_ID_9442,GWAS_ID_9443,GWAS_ID_9444,GWAS_ID_9445,GWAS_ID_9446,GWAS_ID_9447,GWAS_ID_9448,GWAS_ID_9449,GWAS_ID_9450,GWAS_ID_9451,GWAS_ID_9452,GWAS_ID_9453,GWAS_ID_9454,GWAS_ID_9455,GWAS_ID_9456,GWAS_ID_9457,GWAS_ID_9458,GWAS_ID_9459,GWAS_ID_9460,GWAS_ID_9461,GWAS_ID_9462,GWAS_ID_9463,GWAS_ID_9464,GWAS_ID_9465,GWAS_ID_9466,GWAS_ID_9467,GWAS_ID_9468,GWAS_ID_9469,GWAS_ID_9470,GWAS_ID_9471,GWAS_ID_9472,GWAS_ID_9473,GWAS_ID_9474,GWAS_ID_9475,GWAS_ID_9476,GWAS_ID_9477,GWAS_ID_9478,GWAS_ID_9479,GWAS_ID_9480,GWAS_ID_9481,GWAS_ID_9482,GWAS_ID_9483,GWAS_ID_9484,GWAS_ID_9485,GWAS_ID_9486,GWAS_ID_9487,GWAS_ID_9488,GWAS_ID_9489,GWAS_ID_9490,GWAS_ID_9491,GWAS_ID_9492,GWAS_ID_9493,GWAS_ID_9494,GWAS_ID_9495 78557 RMVar_ID_78557 Human_SNP_ID_473291912 m1A Human chr11 - 78079607 78079607 78079607 TTGGGCTACTGCTCCGGCCTGATTGATAACCTAATCCGGCGGAGGCCGATCGCGACGGCTGGTGA TTGGGCTACTGCTCCGGCCTGATTGATAACCTCATCCGGCGGAGGCCGATCGCGACGGCTGGTGA T G NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs534418 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_751380,Human_RBP_ID_4184357,Human_RBP_ID_9276051,Human_RBP_ID_17682689,Human_RBP_ID_17804735,Human_RBP_ID_18974833,Human_RBP_ID_22433211,Human_RBP_ID_22753772,Human_RBP_ID_26410746,Human_RBP_ID_26804018 Human_Splice_Rec_1281771,Human_Splice_Rec_1281773,Human_Splice_Rec_1281777,Human_Splice_Rec_1281781,Human_Splice_Rec_1281791,Human_Splice_Rec_1281795,Human_Splice_Rec_1281799,Human_Splice_Rec_1281801,Human_Splice_Rec_1281805 GWAS_ID_9439,GWAS_ID_9440,GWAS_ID_9441,GWAS_ID_9442,GWAS_ID_9443,GWAS_ID_9444,GWAS_ID_9445,GWAS_ID_9446,GWAS_ID_9447,GWAS_ID_9448,GWAS_ID_9449,GWAS_ID_9450,GWAS_ID_9451,GWAS_ID_9452,GWAS_ID_9453,GWAS_ID_9454,GWAS_ID_9455,GWAS_ID_9456,GWAS_ID_9457,GWAS_ID_9458,GWAS_ID_9459,GWAS_ID_9460,GWAS_ID_9461,GWAS_ID_9462,GWAS_ID_9463,GWAS_ID_9464,GWAS_ID_9465,GWAS_ID_9466,GWAS_ID_9467,GWAS_ID_9468,GWAS_ID_9469,GWAS_ID_9470,GWAS_ID_9471,GWAS_ID_9472,GWAS_ID_9473,GWAS_ID_9474,GWAS_ID_9475,GWAS_ID_9476,GWAS_ID_9477,GWAS_ID_9478,GWAS_ID_9479,GWAS_ID_9480,GWAS_ID_9481,GWAS_ID_9482,GWAS_ID_9483,GWAS_ID_9484,GWAS_ID_9485,GWAS_ID_9486,GWAS_ID_9487,GWAS_ID_9488,GWAS_ID_9489,GWAS_ID_9490,GWAS_ID_9491,GWAS_ID_9492,GWAS_ID_9493,GWAS_ID_9494,GWAS_ID_9495 78558 RMVar_ID_78558 Human_SNP_ID_473291969 m1A Human chr11 + 78079700 78079700 78079700 GTCAGCTTGGGCGGGGGCAGGCTCCGGGCCTCATCCGGCAGAAACCGTAAGGGTTCTGGGTTCCG GTCAGCTTGGGCGGGGGCAGGCTCCGGGCCTCGTCCGGCAGAAACCGTAAGGGTTCTGGGTTCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:78079650..78079875 26863196 MeRIP-seq:(Medium) rs955719985 Functional Loss SNV dbSNP153 33..33 33 - - - 78559 RMVar_ID_78559 Human_SNP_ID_473291999 m1A Human chr11 - 78079773 78079773 78079773 GTCGTGGTTTTCCTTGTAGTTCGTGGTCTGAGACCAGGCCTCAAGTGGAAACGGCGTCACCATGA GTCGTGGTTTTCCTTGTAGTTCGTGGTCTGAGCCCAGGCCTCAAGTGGAAACGGCGTCACCATGA T G NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:78079676..78079850 26863410 MeRIP-seq:(Medium) rs776248652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32425,Human_RBP_ID_404372,Human_RBP_ID_1460592,Human_RBP_ID_4184359,Human_RBP_ID_5282244,Human_RBP_ID_5313814,Human_RBP_ID_5461190,Human_RBP_ID_9276052,Human_RBP_ID_9321749,Human_RBP_ID_17649857,Human_RBP_ID_18613395,Human_RBP_ID_22433214,Human_RBP_ID_23522753,Human_RBP_ID_26897826 78560 RMVar_ID_78560 Human_SNP_ID_473305901 m1A Human chr11 - 78131947 78131947 78131947 TTAGACTATGTTGAGTACTTTAGATTTTATCCAGAGGGCAGAGGCCAGTTAAAAGGGAAATATAA TTAGACTATGTTGAGTACTTTAGATTTTATCCGGAGGGCAGAGGCCAGTTAAAAGGGAAATATAA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:78131945..78132115 26863196 MeRIP-seq:(Medium) rs1015186173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11774933 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 78561 RMVar_ID_78561 Human_SNP_ID_473307737 m1A Human chr11 - 78138815 78138815 78138815 ACAGCATGGGGTGCACTGGGGACAGATAACACAGGGTTTCGAAGACCACAGTTAGACTGCTGTGT ACAGCATGGGGTGCACTGGGGACAGATAACACGGGGTTTCGAAGACCACAGTTAGACTGCTGTGT T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78138809..78138906 26863196 MeRIP-seq:(Medium) rs141536742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31076,Human_RBP_ID_807420,Human_RBP_ID_2286694,Human_RBP_ID_6098062,Human_RBP_ID_11727394 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 78562 RMVar_ID_78562 Human_SNP_ID_473307972 m1A Human chr11 - 78139567 78139567 78139567 GTGCCGCAGCAATGGCGGCGCTCACAATTGCCACGGGTACTGGCAATTGGTTTTCGGCTTTGGCG GTGCCGCAGCAATGGCGGCGCTCACAATTGCCGCGGGTACTGGCAATTGGTTTTCGGCTTTGGCG T C ALG8 Ensembl:ENSG00000159063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:78139378..78139625;chr11:78139400..78139582;chr11:78139435..78139600 26863196 MeRIP-seq:(Medium) rs1408290909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184360,Human_RBP_ID_18417000 Human_Splice_Rec_1281833,Human_Splice_Rec_1281855,Human_Splice_Rec_1281879,Human_Splice_Rec_1281913,Human_Splice_Rec_1281925,Human_Splice_Rec_1281965,Human_Splice_Rec_1281975,Human_Splice_Rec_1281987,Human_Splice_Rec_1281999,Human_Splice_Rec_1282011,Human_Splice_Rec_1282029,Human_Splice_Rec_1282035 Human_miRNA_ID_2027329,Human_miRNA_ID_2678718,Human_miRNA_ID_3080762 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_80459,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152055 78563 RMVar_ID_78563 Human_SNP_ID_473307979 m1A Human chr11 - 78139574 78139574 78139574 GCGTGCGGTGCCGCAGCAATGGCGGCGCTCACAATTGCCACGGGTACTGGCAATTGGTTTTCGGC GCGTGCGGTGCCGCAGCAATGGCGGCGCTCACGATTGCCACGGGTACTGGCAATTGGTTTTCGGC T C ALG8 Ensembl:ENSG00000159063 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:78139453..78139591 26863196 MeRIP-seq:(Medium) rs1347788607 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4184360,Human_RBP_ID_18417000 Human_Splice_Rec_1281833,Human_Splice_Rec_1281855,Human_Splice_Rec_1281879,Human_Splice_Rec_1281913,Human_Splice_Rec_1281925,Human_Splice_Rec_1281965,Human_Splice_Rec_1281975,Human_Splice_Rec_1281987,Human_Splice_Rec_1281999,Human_Splice_Rec_1282011,Human_Splice_Rec_1282029,Human_Splice_Rec_1282035 Human_miRNA_ID_2027329,Human_miRNA_ID_2678718,Human_miRNA_ID_3080762 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_80459,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152055 78564 RMVar_ID_78564 Human_SNP_ID_473316752 m1A Human chr11 - 78174025 78174025 78174025 CTCCAATGGCAATCTCTCCTCCATCACCAGCCACTTGCAGGACCCCAACCACCTGACTCTGGACT CTCCAATGGCAATCTCTCCTCCATCACCAGCCTCTTGCAGGACCCCAACCACCTGACTCTGGACT T A KCTD21 Ensembl:ENSG00000188997 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:78173974..78174125 32194978 MeRIP-seq:(Medium) rs1245584709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27416444,Human_RBP_ID_27557423 78565 RMVar_ID_78565 Human_SNP_ID_473320725 m1A Human chr11 + 78188567 78188567 78188567 GTCCCCGAGCCCCGCGACCCCGGCCGTGCCGCACCCACCTCCTGCCCTCGCTCTGCAGCCTCTCC GTCCCCGAGCCCCGCGACCCCGGCCGTGCCGCGCCCACCTCCTGCCCTCGCTCTGCAGCCTCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78187944..78188591 26863196 MeRIP-seq:(Medium) rs987656589 Functional Loss SNV dbSNP153 33..33 33 - - - 78566 RMVar_ID_78566 Human_SNP_ID_473320918 m1A Human chr11 + 78188994 78188994 78188994 GAGGCTTGTGCCAGGCGGGGTGGGAAGACTGGATTTTGCAGTGGAAGCAGCATCTCTTCCGTCTG GAGGCTTGTGCCAGGCGGGGTGGGAAGACTGGGTTTTGCAGTGGAAGCAGCATCTCTTCCGTCTG A G USP35 Ensembl:ENSG00000118369 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78188894..78189072 26863196 MeRIP-seq:(Medium) rs1163257225 Functional Loss SNV dbSNP153 33..33 33 - - - 78567 RMVar_ID_78567 Human_SNP_ID_473322450 m1A Human chr11 + 78195046 78195046 78195046 AGAGCATACACAAAGGCCCAGGGGCAGAGGGCACACGGTGAGCCAAGGGTGACAGGCCGGTGTGG AGAGCATACACAAAGGCCCAGGGGCAGAGGGCGCACGGTGAGCCAAGGGTGACAGGCCGGTGTGG A G USP35 Ensembl:ENSG00000118369 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:78195041..78195119 26863196 MeRIP-seq:(Medium) rs1405388565 Functional Loss SNV dbSNP153 33..33 33 - - - 78568 RMVar_ID_78568 Human_SNP_ID_473327203 m1A Human chr11 + 78209928 78209928 78209928 GAAGAAGGGAAGGAGGAGAGAACGGAGAAGGAAGAAGTGGGGGAGGAGGAGGAAAGCACCAGAGG GAAGAAGGGAAGGAGGAGAGAACGGAGAAGGAGGAAGTGGGGGAGGAGGAGGAAAGCACCAGAGG A G USP35 Ensembl:ENSG00000118369 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78209794..78210160 26863196 MeRIP-seq:(Medium) rs1323235882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10570,RMVar_hsa_circ_41469,RMVar_hsa_circ_60424 78569 RMVar_ID_78569 Human_SNP_ID_473327255 m1A Human chr11 + 78210026 78210026 78210026 AGAGGAAGAAGAGAAGGTGGAGAAGGAGACAGAAAAGGAGGCTGAGCAGGAAAAGGAAGAAGACA AGAGGAAGAAGAGAAGGTGGAGAAGGAGACAGCAAAGGAGGCTGAGCAGGAAAAGGAAGAAGACA A C USP35 Ensembl:ENSG00000118369 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:78209602..78210087 26863196 MeRIP-seq:(Medium) rs1403638261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10570,RMVar_hsa_circ_41469,RMVar_hsa_circ_60424 78570 RMVar_ID_78570 Human_SNP_ID_473384255 m1A Human chr11 - 78417717 78417717 78417717 GACCCGGCGGGGGGCTCCAGGCCGGCAGCATGAGCGGCGGCGGCGACGTGGTGTGCACCGGCTGG GACCCGGCGGGGGGCTCCAGGCCGGCAGCATGGGCGGCGGCGGCGACGTGGTGTGCACCGGCTGG T C GAB2 Ensembl:ENSG00000033327 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:78417626..78417776 26863196 MeRIP-seq:(Medium) rs1410919622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185305,Human_RBP_ID_8774488,Human_RBP_ID_9276053,Human_RBP_ID_18417001 Human_Splice_Rec_1282173,Human_Splice_Rec_1282211,Human_Splice_Rec_1282221,Human_Splice_Rec_1282227 RMVar_hsa_circ_120932,RMVar_hsa_circ_152064 78571 RMVar_ID_78571 Human_SNP_ID_473384256 m1A Human chr11 + 78417719 78417719 78417719 AGCCGGTGCACACCACGTCGCCGCCGCCGCTCATGCTGCCGGCCTGGAGCCCCCCGCCGGGTCGC AGCCGGTGCACACCACGTCGCCGCCGCCGCTCCTGCTGCCGGCCTGGAGCCCCCCGCCGGGTCGC A C AP003086.1 Ensembl:ENSG00000254420 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78417475..78417807 26863196 MeRIP-seq:(Medium) rs757634170 Functional Loss SNV dbSNP153 33..33 33 - - - 78572 RMVar_ID_78572 Human_SNP_ID_473384259 m1A Human chr11 - 78417723 78417723 78417723 CCGCGCGACCCGGCGGGGGGCTCCAGGCCGGCAGCATGAGCGGCGGCGGCGACGTGGTGTGCACC CCGCGCGACCCGGCGGGGGGCTCCAGGCCGGCGGCATGAGCGGCGGCGGCGACGTGGTGTGCACC T C GAB2 Ensembl:ENSG00000033327 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:78417693..78417788 26863196 MeRIP-seq:(Medium) rs201542938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4179830,Human_RBP_ID_8774488,Human_RBP_ID_9276053,Human_RBP_ID_18417001 Human_Splice_Rec_1282173,Human_Splice_Rec_1282211,Human_Splice_Rec_1282221,Human_Splice_Rec_1282227 RMVar_hsa_circ_120932,RMVar_hsa_circ_152064 78573 RMVar_ID_78573 Human_SNP_ID_473384260 m1A Human chr11 - 78417723 78417723 78417723 CCGCGCGACCCGGCGGGGGGCTCCAGGCCGGCAGCATGAGCGGCGGCGGCGACGTGGTGTGCACC CCGCGCGACCCGGCGGGGGGCTCCAGGCCGGCCGCATGAGCGGCGGCGGCGACGTGGTGTGCACC T G GAB2 Ensembl:ENSG00000033327 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:78417693..78417788 26863196 MeRIP-seq:(Medium) rs201542938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4179830,Human_RBP_ID_8774488,Human_RBP_ID_9276053,Human_RBP_ID_18417001 Human_Splice_Rec_1282173,Human_Splice_Rec_1282211,Human_Splice_Rec_1282221,Human_Splice_Rec_1282227 RMVar_hsa_circ_120932,RMVar_hsa_circ_152064 78574 RMVar_ID_78574 Human_SNP_ID_473406118 m1A Human chr11 - 78498466 78498466 78498466 GCCAGTAAGTAGTTAACTGAAATCATTGGCCAAGGGAAATCATATAAGGAAAAGTATCGGGAGAA GCCAGTAAGTAGTTAACTGAAATCATTGGCCAGGGGAAATCATATAAGGAAAAGTATCGGGAGAA T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:78498444..78498565 26863196 MeRIP-seq:(Medium) rs1362713705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375777,RMVar_hsa_circ_66289,RMVar_hsa_circ_117631,RMVar_hsa_circ_152072,RMVar_hsa_circ_311366,RMVar_hsa_circ_347992,RMVar_hsa_circ_370660,RMVar_hsa_circ_152079,RMVar_hsa_circ_152080,RMVar_hsa_circ_152078,RMVar_hsa_circ_70820,RMVar_hsa_circ_305627,RMVar_hsa_circ_71920,RMVar_hsa_circ_334969,RMVar_hsa_circ_336246,RMVar_hsa_circ_300721 78575 RMVar_ID_78575 Human_SNP_ID_473426728 m1A Human chr11 - 78574632 78574632 78574632 GTGGGGACAGAGCTGGGAGTCCTGAAGGAGAAAGCGCGCAGCCGAGGGGCTCTGGAGTGCCTTAG GTGGGGACAGAGCTGGGAGTCCTGAAGGAGAAGGCGCGCAGCCGAGGGGCTCTGGAGTGCCTTAG T C NARS2 Ensembl:ENSG00000137513 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:78574410..78574825;chr11:78574432..78574825 26863196 MeRIP-seq:(Medium) rs527908311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520908,Human_RBP_ID_22433899 78576 RMVar_ID_78576 Human_SNP_ID_473426733 m1A Human chr11 - 78574636 78574636 78574636 TTCTGTGGGGACAGAGCTGGGAGTCCTGAAGGAGAAAGCGCGCAGCCGAGGGGCTCTGGAGTGCC TTCTGTGGGGACAGAGCTGGGAGTCCTGAAGGGGAAAGCGCGCAGCCGAGGGGCTCTGGAGTGCC T C NARS2 Ensembl:ENSG00000137513 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr11:78574417..78574825;chr11:78574533..78574747 26863196 MeRIP-seq:(Medium) rs1244229274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520908,Human_RBP_ID_22433899 78577 RMVar_ID_78577 Human_SNP_ID_434563921 m1A Human chr10 - 60778560 60778560 60778560 ACCCTGACCCCAGCCACTGTACCCGGCTTATTATTCCGCGGCGGCCGCAGCGGCAGCTACAACAA ACCCTGACCCCAGCCACTGTACCCGGCTTATTTTTCCGCGGCGGCCGCAGCGGCAGCTACAACAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:60778548..60778731 26863196 MeRIP-seq:(Medium) rs947728550 Functional Loss SNV dbSNP153 33..33 33 - - - 78578 RMVar_ID_78578 Human_SNP_ID_434563946 m1A Human chr10 + 60778631 60778631 60778631 TAGGGGACGGCCGAGGGCCTCGGAGGGCGAGTATTGAGGAACGGGGTCCTCTAAGAAGGCCGGAC TAGGGGACGGCCGAGGGCCTCGGAGGGCGAGTTTTGAGGAACGGGGTCCTCTAAGAAGGCCGGAC A T CDK1 Ensembl:ENSG00000170312 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:60778571..60778708 26863196 MeRIP-seq:(Medium) rs944487618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4122588,Human_RBP_ID_5339169,Human_RBP_ID_5983171,Human_RBP_ID_9320561,Human_RBP_ID_19045362,Human_RBP_ID_27836013 Human_Splice_Rec_1137135 78579 RMVar_ID_78579 Human_SNP_ID_434564355 m1A Human chr10 - 60780194 60780194 60780194 ATTTATTTTACTAAAACCACTCACCTTCTCCAATTTTCTCTATTTTGGTATAATCTTCCATAGTT ATTTATTTTACTAAAACCACTCACCTTCTCCAGTTTTCTCTATTTTGGTATAATCTTCCATAGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:60778476..60780261;chr10:60780126..60780225 26863196 MeRIP-seq:(Medium) rs745479111 Functional Loss SNV dbSNP153 33..33 33 - - - 78580 RMVar_ID_78580 Human_SNP_ID_434565320 m1A Human chr10 + 60784757 60784757 60784757 AAGGGTAGACACAAAACTACAGGTCAAGTGGTAGCCATGAAAAAAATCAGACTAGAAAGTGAAGA AAGGGTAGACACAAAACTACAGGTCAAGTGGTGGCCATGAAAAAAATCAGACTAGAAAGTGAAGA A G CDK1 Ensembl:ENSG00000170312 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:60784645..60784800 26863196 MeRIP-seq:(Medium) rs774991794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_379514,Human_RBP_ID_861550,Human_RBP_ID_1159215,Human_RBP_ID_1352235,Human_RBP_ID_1447926,Human_RBP_ID_1768137,Human_RBP_ID_2222820,Human_RBP_ID_3353326,Human_RBP_ID_4122591,Human_RBP_ID_8761808,Human_RBP_ID_8990257,Human_RBP_ID_11383906,Human_RBP_ID_17779607,Human_RBP_ID_18595636,Human_RBP_ID_22431418,Human_RBP_ID_27609039 Human_Splice_Rec_1137096,Human_Splice_Rec_1137104,Human_Splice_Rec_1137110,Human_Splice_Rec_1137126,Human_Splice_Rec_1137138,Human_Splice_Rec_1137152,Human_Splice_Rec_1137162 Human_miRNA_ID_256634,Human_miRNA_ID_260428 RMVar_hsa_circ_13223,RMVar_hsa_circ_339113,RMVar_hsa_circ_347512,RMVar_hsa_circ_143568 78581 RMVar_ID_78581 Human_SNP_ID_434567957 m1A Human chr10 + 60796639 60796638 60796640 ATAGAGGGGTAAATTAAAGCTGAGAAGACTGAAGAGAGAGGTATTTCAGACTAAAAAATAGGGCC ATAGAGGGGTAAATTAAAGCTGAGAAGACTGA__AGAGAGGTATTTCAGACTAAAAAATAGGGCC AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:60796594..60796697 26863196 MeRIP-seq:(Medium) rs1203513115 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5983588,Human_RBP_ID_11384465,Human_RBP_ID_23461944 78582 RMVar_ID_78582 Human_SNP_ID_434843604 m1A Human chr10 - 61903407 61903407 61903407 GAGGAGGGGAGCCCGCAGAACTGCGGTCACACATGAAATGACAGAGCCGAAGGGAGGCGGCCGCC GAGGAGGGGAGCCCGCAGAACTGCGGTCACACTTGAAATGACAGAGCCGAAGGGAGGCGGCCGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:61903358..61903453 26863196 MeRIP-seq:(Medium) rs1401977686 Functional Loss SNV dbSNP153 33..33 33 - - - 78583 RMVar_ID_78583 Human_SNP_ID_434843605 m1A Human chr10 - 61903407 61903407 61903407 GAGGAGGGGAGCCCGCAGAACTGCGGTCACACATGAAATGACAGAGCCGAAGGGAGGCGGCCGCC GAGGAGGGGAGCCCGCAGAACTGCGGTCACACGTGAAATGACAGAGCCGAAGGGAGGCGGCCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:61903358..61903453 26863196 MeRIP-seq:(Medium) rs1401977686 Functional Loss SNV dbSNP153 33..33 33 - - - 78584 RMVar_ID_78584 Human_SNP_ID_434915756 m1A Human chr10 + 62212728 62212728 62212728 CTGTCTCAAACAAACAAACAAACAAAAAACCAAAAAGAAAACGCTAATAGCATGTCTCCCTTACA CTGTCTCAAACAAACAAACAAACAAAAAACCAGAAAGAAAACGCTAATAGCATGTCTCCCTTACA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:62212608..62212735 26863196 MeRIP-seq:(Medium) rs1414114098 Functional Loss SNV dbSNP153 33..33 33 - - - 78585 RMVar_ID_78585 Human_SNP_ID_435059656 m1A Human chr10 + 62804966 62804966 62804966 ACGGGCCGGTGGTTGCGGGGCCTCCCGCCTCGACCCGGGCTGGGGGCAGCCGTGGCGGCCGCCGG ACGGGCCGGTGGTTGCGGGGCCTCCCGCCTCGGCCCGGGCTGGGGGCAGCCGTGGCGGCCGCCGG A G ADO Ensembl:ENSG00000181915 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:62804888..62804972 26863410 MeRIP-seq:(Medium) rs1165690501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4123028 78586 RMVar_ID_78586 Human_SNP_ID_435141260 m1A Human chr10 - 63133380 63133380 63133380 GGGGACTGCAAGGGAGCTCGACGCAGCCGCGGAGACTGCGGCCCCTCTCTGCGCCCCAAGAGCCA GGGGACTGCAAGGGAGCTCGACGCAGCCGCGGGGACTGCGGCCCCTCTCTGCGCCCCAAGAGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63133330..63133538 26863196 MeRIP-seq:(Medium) rs756630994 Functional Loss SNV dbSNP153 33..33 33 - - - 78587 RMVar_ID_78587 Human_SNP_ID_435141276 m1A Human chr10 - 63133408 63133400 63133408 GGGGAGTAGTGGCGCCGGGGAACATGGAGGGGACTGCAAGGGAGCTCGACGCAGCCGCGGAGACT GGGGAGTAGTGGCGCCGGGGAACATGGAGGGG________GGAGCTCGACGCAGCCGCGGAGACT CCTTGCAGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:63133359..63133491;chr10:63133358..63133449 26863196 MeRIP-seq:(Medium) rs546290609 Functional Loss DEL dbSNP153 33..40 33 - - - 78588 RMVar_ID_78588 Human_SNP_ID_435141297 m1A Human chr10 + 63133431 63133431 63133431 CCCTTGCAGTCCCCTCCATGTTCCCCGGCGCCACTACTCCCCTTCCTAAGGCCGCCGCTTACCCC CCCTTGCAGTCCCCTCCATGTTCCCCGGCGCCGCTACTCCCCTTCCTAAGGCCGCCGCTTACCCC A G NRBF2 Ensembl:ENSG00000148572 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:63133342..63133455 26863196 MeRIP-seq:(Medium) rs1191486339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136289,Human_RBP_ID_5488328,Human_RBP_ID_17780132 Human_Splice_Rec_1137571,Human_Splice_Rec_1137575 RMVar_hsa_circ_126098,RMVar_hsa_circ_143591 78589 RMVar_ID_78589 Human_SNP_ID_435208315 m1A Human chr10 - 63380478 63380478 63380478 ATTGAATTTTGTGTTTTTGTTTTCATAGGTGTATGTGGAATTTGATGATCTTGAATGGGATAAAC ATTGAATTTTGTGTTTTTGTTTTCATAGGTGTGTGTGGAATTTGATGATCTTGAATGGGATAAAC T C JMJD1C Ensembl:ENSG00000171988 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63380388..63380525 26863196 MeRIP-seq:(Medium) rs1451725739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4142512,Human_RBP_ID_9601385,Human_RBP_ID_11389775 Human_Splice_Rec_1137628,Human_Splice_Rec_1137816 RMVar_hsa_circ_84267,RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631,RMVar_hsa_circ_106801,RMVar_hsa_circ_273333,RMVar_hsa_circ_143633,RMVar_hsa_circ_143635,RMVar_hsa_circ_143636,RMVar_hsa_circ_143637,RMVar_hsa_circ_143634 78590 RMVar_ID_78590 Human_SNP_ID_435208316 m1A Human chr10 + 63380479 63380479 63380479 TTTATCCCATTCAAGATCATCAAATTCCACATACACCTATGAAAACAAAAACACAAAATTCAATT TTTATCCCATTCAAGATCATCAAATTCCACATGCACCTATGAAAACAAAAACACAAAATTCAATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:63380455..63380542 26863196 MeRIP-seq:(Medium) rs1170410454 Functional Loss SNV dbSNP153 33..33 33 - - - 78591 RMVar_ID_78591 Human_SNP_ID_435231550 m1A Human chr10 + 63465245 63465245 63465245 CACAGCGGGGAGCCGCGGTCGACCCCTCCGGGATGGGGGCCAGGGCAGCCTCCGCGGCTATCCCG CACAGCGGGGAGCCGCGGTCGACCCCTCCGGGTTGGGGGCCAGGGCAGCCTCCGCGGCTATCCCG A T JMJD1C-AS1 Ensembl:ENSG00000272767 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63465242..63465314 26863196 MeRIP-seq:(Medium) rs1024182484 Functional Loss SNV dbSNP153 33..33 33 - - - 78592 RMVar_ID_78592 Human_SNP_ID_435231693 m1A Human chr10 - 63465487 63465487 63465487 GGACAGCCGCAATCCGGACCTGGCGGTAAGAGAGTCAGCGCCCCCCTTTTCCCCTGCCGCGCCCG GGACAGCCGCAATCCGGACCTGGCGGTAAGAGCGTCAGCGCCCCCCTTTTCCCCTGCCGCGCCCG T G JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:63465475..63465921 32194978 MeRIP-seq:(Medium) rs1483579741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143637 78593 RMVar_ID_78593 Human_SNP_ID_435231715 m1A Human chr10 + 63465507 63465507 63465507 GGGGGCGCTGACTCTCTTACCGCCAGGTCCGGATTGCGGCTGTCCCTGTGTGACACGGCTCGGAT GGGGGCGCTGACTCTCTTACCGCCAGGTCCGGCTTGCGGCTGTCCCTGTGTGACACGGCTCGGAT A C JMJD1C-AS1 Ensembl:ENSG00000272767 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63465496..63465771 26863196 MeRIP-seq:(Medium) rs1363936925 Functional Loss SNV dbSNP153 33..33 33 - - - 78594 RMVar_ID_78594 Human_SNP_ID_435231792 m1A Human chr10 + 63465613 63465611 63465613 AGCGCTCCGAACGTGCCTCGTCGCCGACCGCCACACACAGGAACCGCTTACCCACCAGCTCTGCC AGCGCTCCGAACGTGCCTCGTCGCCGACCGC__CACACAGGAACCGCTTACCCACCAGCTCTGCC CCA C JMJD1C-AS1 Ensembl:ENSG00000272767 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:63465532..63465690 26863196 MeRIP-seq:(Medium) rs1030545481 Functional Loss DEL dbSNP153 32..33 33 - - - 78595 RMVar_ID_78595 Human_SNP_ID_435231793 m1A Human chr10 + 63465613 63465613 63465613 AGCGCTCCGAACGTGCCTCGTCGCCGACCGCCACACACAGGAACCGCTTACCCACCAGCTCTGCC AGCGCTCCGAACGTGCCTCGTCGCCGACCGCCGCACACAGGAACCGCTTACCCACCAGCTCTGCC A G JMJD1C-AS1 Ensembl:ENSG00000272767 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:63465532..63465690 26863196 MeRIP-seq:(Medium) rs953648309 Functional Loss SNV dbSNP153 33..33 33 - - - 78596 RMVar_ID_78596 Human_SNP_ID_435245792 m1A Human chr10 - 63521479 63521479 63521479 GTGGGCGCAGGGCGCTGCGGACCAGGCCGCCAACGGCAGGCCGCGCGCTTCGCCGGCTCCTCGCG GTGGGCGCAGGGCGCTGCGGACCAGGCCGCCAGCGGCAGGCCGCGCGCTTCGCCGGCTCCTCGCG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63521441..63521525 26863196 MeRIP-seq:(Medium) rs948639924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26754064,Human_RBP_ID_26775242 78597 RMVar_ID_78597 Human_SNP_ID_435245889 m1A Human chr10 - 63521761 63521761 63521761 TCGCCGCAGCTAGGCCCTCGGCCGTCGCAGGGAGCTCCGCAGCGACGTGGACCAAGGTGAGGAAG TCGCCGCAGCTAGGCCCTCGGCCGTCGCAGGGGGCTCCGCAGCGACGTGGACCAAGGTGAGGAAG T C JMJD1C Ensembl:ENSG00000171988 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:63521751..63521841;chr10:63521738..63521965 26863196 MeRIP-seq:(Medium) rs1395303132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136293,Human_RBP_ID_18416118,Human_RBP_ID_27802726 Human_Splice_Rec_1137815 78598 RMVar_ID_78598 Human_SNP_ID_435252236 m1A Human chr10 + 63549820 63549818 63549821 AGCTAGAATGATCCACGTGGGGAAGAGGAAAGATGAGGAGGGAAGGAGGCATTCCAGCTAAGAAT AGCTAGAATGATCCACGTGGGGAAGAGGAAA___GAGGAGGGAAGGAGGCATTCCAGCTAAGAAT AGAT A REEP3 Ensembl:ENSG00000165476 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:63549817..63549961 26863196 MeRIP-seq:(Medium) rs921167159 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5987264 78599 RMVar_ID_78599 Human_SNP_ID_436282497 m1A Human chr10 + 67764544 67764544 67764544 GCCGAGTGGTTAAGGCGTTGGACTTGAAATCCAATGGGGTCTCCCCGCGCAGGTTCGAACCCTGC GCCGAGTGGTTAAGGCGTTGGACTTGAAATCCCATGGGGTCTCCCCGCGCAGGTTCGAACCCTGC A C tRNA-Ser-TGA-1-1 RNACentral:URS0000092302 tRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:67764501..67764636 26863196 MeRIP-seq:(Medium) rs1432846531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273933,Human_RBP_ID_380085,Human_RBP_ID_1159352,Human_RBP_ID_1448491,Human_RBP_ID_1768838,Human_RBP_ID_2225593,Human_RBP_ID_3354502,Human_RBP_ID_4142553,Human_RBP_ID_5092914,Human_RBP_ID_5162422,Human_RBP_ID_5254945,Human_RBP_ID_5273575,Human_RBP_ID_5415213,Human_RBP_ID_5435589,Human_RBP_ID_5488358,Human_RBP_ID_6033052,Human_RBP_ID_8244636,Human_RBP_ID_8337019,Human_RBP_ID_8991102,Human_RBP_ID_11392599,Human_RBP_ID_17073552,Human_RBP_ID_17347025,Human_RBP_ID_17581318,Human_RBP_ID_17780566,Human_RBP_ID_18175846,Human_RBP_ID_18205527,Human_RBP_ID_18510189,Human_RBP_ID_18596260,Human_RBP_ID_19534416,Human_RBP_ID_22377921,Human_RBP_ID_22788368,Human_RBP_ID_22883309,Human_RBP_ID_23123756,Human_RBP_ID_23152315,Human_RBP_ID_23463498,Human_RBP_ID_24402633,Human_RBP_ID_24457235,Human_RBP_ID_26747456,Human_RBP_ID_26880669,Human_RBP_ID_27194086,Human_RBP_ID_27406596 78600 RMVar_ID_78600 Human_SNP_ID_436312756 m1A Human chr10 + 67885004 67885004 67885004 CGGCGGCAGGCGGGGAGCAAGAGGCCCAGGCGACTGCGGCGGCTGGGGAAGGAGACAATGGGCCG CGGCGGCAGGCGGGGAGCAAGAGGCCCAGGCGTCTGCGGCGGCTGGGGAAGGAGACAATGGGCCG A T SIRT1 Ensembl:ENSG00000096717 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr10:67884738..67885100;chr10:67884914..67885110;chr10:67884903..67885090 26863196 MeRIP-seq:(Medium) rs767360333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748433,Human_RBP_ID_18970765,Human_RBP_ID_26317201 78601 RMVar_ID_78601 Human_SNP_ID_436313711 m1A Human chr10 + 67887375 67887375 67887375 TTGCTCTATAACCGTTCATACATTTTAGGTGCATGTTGTTTTGATAGCCTTGACTGACTTGGTTT TTGCTCTATAACCGTTCATACATTTTAGGTGCGTGTTGTTTTGATAGCCTTGACTGACTTGGTTT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:67887373..67887489 26863196 MeRIP-seq:(Medium) rs767214023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17595012,Human_RBP_ID_22536959,Human_RBP_ID_22639352,Human_RBP_ID_22735717 78602 RMVar_ID_78602 Human_SNP_ID_436314183 m1A Human chr10 - 67888844 67888844 67888844 ATAAGGGGGAAAAGGCTTAAAGTCAACTTATCAAGTAATTCAAAATCTCATTTATTTTCTGAAGT ATAAGGGGGAAAAGGCTTAAAGTCAACTTATCGAGTAATTCAAAATCTCATTTATTTTCTGAAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:67888838..67888967 26863196 MeRIP-seq:(Medium) rs753163477 Functional Loss SNV dbSNP153 33..33 33 - - - 78603 RMVar_ID_78603 Human_SNP_ID_436361103 m1A Human chr10 + 68075233 68075233 68075233 CGACCCGGATGGAGCGGGCGGGGAAGAACGGGAGGCAAGCGGGGCGGAGAGCACCAGGGGTGGGG CGACCCGGATGGAGCGGGCGGGGAAGAACGGGGGGCAAGCGGGGCGGAGAGCACCAGGGGTGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68074753..68075300 26863196 MeRIP-seq:(Medium) rs1455307485 Functional Loss SNV dbSNP153 33..33 33 - - - 78604 RMVar_ID_78604 Human_SNP_ID_436365960 m1A Human chr10 + 68095734 68095734 68095734 TAGCAAGACAAAGTCCTAGGGACAGAAAGGAGAATGGTGGTTGCCAGCAGTTGGGGGAAGAGGGG TAGCAAGACAAAGTCCTAGGGACAGAAAGGAGCATGGTGGTTGCCAGCAGTTGGGGGAAGAGGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68095695..68095839 26863196 MeRIP-seq:(Medium) rs931952294 Functional Loss SNV dbSNP153 33..33 33 - - - 78605 RMVar_ID_78605 Human_SNP_ID_436383065 m1A Human chr10 - 68166394 68166394 68166394 AGTTTGGGTTTGGGGGGTTGTTCCACAGATGGAGGCTCTGAGTGGGGTGGGGAGGGCTGTGGCTC AGTTTGGGTTTGGGGGGTTGTTCCACAGATGGGGGCTCTGAGTGGGGTGGGGAGGGCTGTGGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:68166345..68166557 26863196 MeRIP-seq:(Medium) rs1335194362 Functional Loss SNV dbSNP153 33..33 33 - - - 78606 RMVar_ID_78606 Human_SNP_ID_436385263 m1A Human chr10 + 68174471 68174471 68174471 GAGCCACTCCCACCAGGCCCAACAGAACCAACACCACCACCATTCACATTTTCCATCCCCAGCGG GAGCCACTCCCACCAGGCCCAACAGAACCAACCCCACCACCATTCACATTTTCCATCCCCAGCGG A C MYPN Ensembl:ENSG00000138347 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68174422..68174546 26863196 MeRIP-seq:(Medium) rs1190436982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28806,Human_RBP_ID_2227496 RMVar_hsa_circ_5621,RMVar_hsa_circ_3885,RMVar_hsa_circ_337726,RMVar_hsa_circ_44956,RMVar_hsa_circ_10922,RMVar_hsa_circ_346988 78607 RMVar_ID_78607 Human_SNP_ID_436385264 m1A Human chr10 + 68174471 68174471 68174471 GAGCCACTCCCACCAGGCCCAACAGAACCAACACCACCACCATTCACATTTTCCATCCCCAGCGG GAGCCACTCCCACCAGGCCCAACAGAACCAACGCCACCACCATTCACATTTTCCATCCCCAGCGG A G MYPN Ensembl:ENSG00000138347 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68174422..68174546 26863196 MeRIP-seq:(Medium) rs1190436982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28806,Human_RBP_ID_2227496 RMVar_hsa_circ_5621,RMVar_hsa_circ_3885,RMVar_hsa_circ_337726,RMVar_hsa_circ_44956,RMVar_hsa_circ_10922,RMVar_hsa_circ_346988 78608 RMVar_ID_78608 Human_SNP_ID_436388150 m1A Human chr10 + 68185195 68185195 68185195 AAGGAGGGAAGGAGGGAAGGAGGGAAGGAGGGAAGGAAGGGAGGAAGGGAAGAAGTGAAAAGAAA AAGGAGGGAAGGAGGGAAGGAGGGAAGGAGGGGAGGAAGGGAGGAAGGGAAGAAGTGAAAAGAAA A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68185183..68185286 26863196 MeRIP-seq:(Medium) rs1020413385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44956,RMVar_hsa_circ_26181,RMVar_hsa_circ_335583,RMVar_hsa_circ_276076,RMVar_hsa_circ_143725 78609 RMVar_ID_78609 Human_SNP_ID_436423670 m1A Human chr10 + 68332120 68332120 68332120 AAGCGGTTGTCACCGCTGGAGACGGTTGGGAGAACCGTTGTGGCGAGCGCTACACGAGGCAAACG AAGCGGTTGTCACCGCTGGAGACGGTTGGGAGGACCGTTGTGGCGAGCGCTACACGAGGCAAACG A G HNRNPH3 Ensembl:ENSG00000096746 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:68332076..68332427 26863196 MeRIP-seq:(Medium) rs1397498444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225686,Human_RBP_ID_380194,Human_RBP_ID_1448559,Human_RBP_ID_4123676,Human_RBP_ID_5435596,Human_RBP_ID_5989156,Human_RBP_ID_9273814,Human_RBP_ID_9320571,Human_RBP_ID_11396087,Human_RBP_ID_18416120,Human_RBP_ID_18596363,Human_RBP_ID_22029301,Human_RBP_ID_22886803,Human_RBP_ID_23117809,Human_RBP_ID_23123763,Human_RBP_ID_26880730 Human_Splice_Rec_1139053,Human_Splice_Rec_1139075,Human_Splice_Rec_1139103,Human_Splice_Rec_1139117 78610 RMVar_ID_78610 Human_SNP_ID_436423672 m1A Human chr10 - 68332125 68332125 68332125 GAAGTCGTTTGCCTCGTGTAGCGCTCGCCACAACGGTTCTCCCAACCGTCTCCAGCGGTGACAAC GAAGTCGTTTGCCTCGTGTAGCGCTCGCCACAGCGGTTCTCCCAACCGTCTCCAGCGGTGACAAC T C PBLD Ensembl:ENSG00000108187 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68332076..68332388 26863196 MeRIP-seq:(Medium) rs1029501210 Functional Loss SNV dbSNP153 33..33 33 - - - 78611 RMVar_ID_78611 Human_SNP_ID_436423673 m1A Human chr10 - 68332126 68332126 68332126 AGAAGTCGTTTGCCTCGTGTAGCGCTCGCCACAACGGTTCTCCCAACCGTCTCCAGCGGTGACAA AGAAGTCGTTTGCCTCGTGTAGCGCTCGCCACGACGGTTCTCCCAACCGTCTCCAGCGGTGACAA T C PBLD Ensembl:ENSG00000108187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68332076..68332442 26863196 MeRIP-seq:(Medium) rs774960777 Functional Loss SNV dbSNP153 33..33 33 - - - 78612 RMVar_ID_78612 Human_SNP_ID_436423689 m1A Human chr10 - 68332155 68332155 68332155 GTGCTCGCGGGGTCCAGTTCAAAGAAGGGAGAAGTCGTTTGCCTCGTGTAGCGCTCGCCACAACG GTGCTCGCGGGGTCCAGTTCAAAGAAGGGAGACGTCGTTTGCCTCGTGTAGCGCTCGCCACAACG T G PBLD Ensembl:ENSG00000108187 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:68332068..68332219 32194978 MeRIP-seq:(Medium) rs1229467909 Functional Loss SNV dbSNP153 33..33 33 - - - 78613 RMVar_ID_78613 Human_SNP_ID_436425329 m1A Human chr10 + 68338587 68338587 68338587 CCACCAAGAAGATTGCTGGGACAGCGACCGGGACCATATGATAGACCAATAGGAGGAAGAGGGGG CCACCAAGAAGATTGCTGGGACAGCGACCGGGCCCATATGATAGACCAATAGGAGGAAGAGGGGG A C HNRNPH3 Ensembl:ENSG00000096746 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:68338501..68338712;chr10:68338501..68338846 26863196 MeRIP-seq:(Medium) rs776547177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1448625,Human_RBP_ID_1769055,Human_RBP_ID_5989389,Human_RBP_ID_8762333,Human_RBP_ID_9360386,Human_RBP_ID_11396490,Human_RBP_ID_17780706,Human_RBP_ID_18431869,Human_RBP_ID_18525059,Human_RBP_ID_22883449,Human_RBP_ID_23112908,Human_RBP_ID_23117781,Human_RBP_ID_23463908,Human_RBP_ID_26316329,Human_RBP_ID_27609854 Human_Splice_Rec_1139070,Human_Splice_Rec_1139080,Human_Splice_Rec_1139096,Human_Splice_Rec_1139097,Human_Splice_Rec_1139108,Human_Splice_Rec_1139116,Human_Splice_Rec_1139122,Human_Splice_Rec_1139123,Human_Splice_Rec_1139148 RMVar_hsa_circ_321716,RMVar_hsa_circ_359868,RMVar_hsa_circ_364113,RMVar_hsa_circ_376301,RMVar_hsa_circ_357669,RMVar_hsa_circ_84362,RMVar_hsa_circ_127023,RMVar_hsa_circ_74024,RMVar_hsa_circ_51438,RMVar_hsa_circ_143734,RMVar_hsa_circ_143736,RMVar_hsa_circ_143737,RMVar_hsa_circ_143735,RMVar_hsa_circ_143733 78614 RMVar_ID_78614 Human_SNP_ID_436425579 m1A Human chr10 - 68339428 68339427 68339429 CATAGCCATGTCCTCCCATACCTGGAAAACACAATTTGCCAAGATTATAAACTATTACAGATACA CATAGCCATGTCCTCCCATACCTGGAAAACA__ATTTGCCAAGATTATAAACTATTACAGATACA TTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:68339426..68339450 26863196 MeRIP-seq:(Medium) rs764226914 Functional Loss DEL dbSNP153 32..33 33 - - - 78615 RMVar_ID_78615 Human_SNP_ID_436426086 m1A Human chr10 - 68341272 68341272 68341272 TTATTTTTATCTTTAGACATGGCAGCTACTGCATCTTCATGTGTCACAAACTCTACATCTGCTTC TTATTTTTATCTTTAGACATGGCAGCTACTGCGTCTTCATGTGTCACAAACTCTACATCTGCTTC T C RUFY2 Ensembl:ENSG00000204130 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68341222..68341319 26863196 MeRIP-seq:(Medium) rs1444886674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1139208,Human_Splice_Rec_1139220,Human_Splice_Rec_1139228 RMVar_hsa_circ_143741 78616 RMVar_ID_78616 Human_SNP_ID_436426622 m1A Human chr10 - 68343092 68343092 68343092 ATTCACATCAACAGGTTTCATTTTGATCCATTAGCCAATTTGGAAAAAAGCCATATTGATCAAAG ATTCACATCAACAGGTTTCATTTTGATCCATTCGCCAATTTGGAAAAAAGCCATATTGATCAAAG T G RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:68343041..68343141 32194978 MeRIP-seq:(Medium) rs1448399314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143741 78617 RMVar_ID_78617 Human_SNP_ID_436443539 m1A Human chr10 + 68407219 68407219 68407219 CATGGCGGCGGCGGCTGCGCGGTCTCGGGCGGAGGCTCCCTCGGCCTGTCCAGCAGCTCCTTCCA CATGGCGGCGGCGGCTGCGCGGTCTCGGGCGGCGGCTCCCTCGGCCTGTCCAGCAGCTCCTTCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:68407136..68407242 26863196 MeRIP-seq:(Medium) rs1161496945 Functional Loss SNV dbSNP153 33..33 33 - - - 78618 RMVar_ID_78618 Human_SNP_ID_436450710 m1A Human chr10 + 68432931 68432931 68432931 TCTGGTATTCCCTAGAGTCCCTTCCCTGGTTCATTGTACTACTCTTTCTCATTGTTTGCTCCAGG TCTGGTATTCCCTAGAGTCCCTTCCCTGGTTCGTTGTACTACTCTTTCTCATTGTTTGCTCCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68432881..68433014 26863196 MeRIP-seq:(Medium) rs1053072095 Functional Loss SNV dbSNP153 33..33 33 - - - 78619 RMVar_ID_78619 Human_SNP_ID_436450711 m1A Human chr10 - 68432935 68432935 68432935 GGACCCTGGAGCAAACAATGAGAAAGAGTAGTACAATGAACCAGGGAAGGGACTCTAGGGAATAC GGACCCTGGAGCAAACAATGAGAAAGAGTAGTGCAATGAACCAGGGAAGGGACTCTAGGGAATAC T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68432887..68432971 26863196 MeRIP-seq:(Medium) rs895467673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11398298 RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,RMVar_hsa_circ_370626,RMVar_hsa_circ_143783,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_24880,RMVar_hsa_circ_143785,RMVar_hsa_circ_331094,RMVar_hsa_circ_347913,RMVar_hsa_circ_273623,RMVar_hsa_circ_40520,RMVar_hsa_circ_31008,RMVar_hsa_circ_101313,RMVar_hsa_circ_143789,RMVar_hsa_circ_143790,RMVar_hsa_circ_143791,RMVar_hsa_circ_369697,RMVar_hsa_circ_8944,RMVar_hsa_circ_36806,RMVar_hsa_circ_122574,RMVar_hsa_circ_121562,RMVar_hsa_circ_143792,RMVar_hsa_circ_143793,RMVar_hsa_circ_143794,RMVar_hsa_circ_360481,RMVar_hsa_circ_340990,RMVar_hsa_circ_315369,RMVar_hsa_circ_321724,RMVar_hsa_circ_313007,RMVar_hsa_circ_300476,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143798,RMVar_hsa_circ_143800,RMVar_hsa_circ_143799,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_334400,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_50387,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_65353,RMVar_hsa_circ_143803,RMVar_hsa_circ_143804,RMVar_hsa_circ_305904,RMVar_hsa_circ_319245,RMVar_hsa_circ_18386,RMVar_hsa_circ_42954,RMVar_hsa_circ_143805,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808 78620 RMVar_ID_78620 Human_SNP_ID_436457183 m1A Human chr10 + 68457421 68457421 68457421 CTTCATTTCCTTTAAGCTTCTGCTCAAATGCTACCTTATGAGGAAGGCCTTCCATGAACATTCTA CTTCATTTCCTTTAAGCTTCTGCTCAAATGCTGCCTTATGAGGAAGGCCTTCCATGAACATTCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68457376..68457497 26863196 MeRIP-seq:(Medium) rs982203971 Functional Loss SNV dbSNP153 33..33 33 - - - 78621 RMVar_ID_78621 Human_SNP_ID_436461161 m1A Human chr10 - 68471867 68471867 68471867 TTTTCTGTCTACAGTTTGCGATCCCCGCGTCCAGGATGGAGCAGCTGAACGAACTGGAGCTGCTG TTTTCTGTCTACAGTTTGCGATCCCCGCGTCCGGGATGGAGCAGCTGAACGAACTGGAGCTGCTG T C DNA2 Ensembl:ENSG00000138346 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:68471630..68471913 26863196 MeRIP-seq:(Medium) rs1171959447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_380318,Human_RBP_ID_3937740,Human_RBP_ID_4123872,Human_RBP_ID_9320572,Human_RBP_ID_18596533,Human_RBP_ID_24825003 Human_Splice_Rec_1139389,Human_Splice_Rec_1139419,Human_Splice_Rec_1139458,Human_Splice_Rec_1139459,Human_Splice_Rec_1139498,Human_Splice_Rec_1139499,Human_Splice_Rec_1139553 RMVar_hsa_circ_8944,RMVar_hsa_circ_45606,RMVar_hsa_circ_122574,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_41530,RMVar_hsa_circ_340697,RMVar_hsa_circ_143828,RMVar_hsa_circ_320365,RMVar_hsa_circ_143829,RMVar_hsa_circ_143827 78622 RMVar_ID_78622 Human_SNP_ID_436461167 m1A Human chr10 + 68471878 68471878 68471878 GTTCGTTCAGCTGCTCCATCCTGGACGCGGGGATCGCAAACTGTAGACAGAAAAGACAGCGGAAC GTTCGTTCAGCTGCTCCATCCTGGACGCGGGGTTCGCAAACTGTAGACAGAAAAGACAGCGGAAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:68471730..68471881 26863196 MeRIP-seq:(Medium) rs1432447757 Functional Loss SNV dbSNP153 33..33 33 - - - 78623 RMVar_ID_78623 Human_SNP_ID_436535816 m1A Human chr10 + 68747474 68747474 68747474 AACATTTGGTGTTCAGACTCAGCCCCAGCCCCAGTCACTGCTGCAGGCACAGATTTCAGCAGCTT AACATTTGGTGTTCAGACTCAGCCCCAGCCCCCGTCACTGCTGCAGGCACAGATTTCAGCAGCTT A C CCAR1 Ensembl:ENSG00000060339 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:68747423..68747599 26863196 MeRIP-seq:(Medium) rs145396018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401137,Human_RBP_ID_17229295,Human_RBP_ID_17345877,Human_RBP_ID_18596633 Human_Splice_Rec_1139669,Human_Splice_Rec_1139723,Human_Splice_Rec_1139769,Human_Splice_Rec_1139797,Human_Splice_Rec_1139827,Human_Splice_Rec_1139869,Human_Splice_Rec_1139911,Human_Splice_Rec_1139939,Human_Splice_Rec_1139975 Human_miRNA_ID_39978,Human_miRNA_ID_68698,Human_miRNA_ID_203704,Human_miRNA_ID_596116,Human_miRNA_ID_1043616,Human_miRNA_ID_1376663,Human_miRNA_ID_1488767,Human_miRNA_ID_2037210,Human_miRNA_ID_2347912 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_143881,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_321608,RMVar_hsa_circ_344019,RMVar_hsa_circ_67297,RMVar_hsa_circ_143887,RMVar_hsa_circ_290656,RMVar_hsa_circ_337403,RMVar_hsa_circ_12406,RMVar_hsa_circ_143891,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143892,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_326519,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_58894,RMVar_hsa_circ_143896,RMVar_hsa_circ_362195,RMVar_hsa_circ_319311,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_274814,RMVar_hsa_circ_12168,RMVar_hsa_circ_29756,RMVar_hsa_circ_143898,RMVar_hsa_circ_143899,RMVar_hsa_circ_278624,RMVar_hsa_circ_338572,RMVar_hsa_circ_47142,RMVar_hsa_circ_143900 78624 RMVar_ID_78624 Human_SNP_ID_436539680 m1A Human chr10 + 68761125 68761125 68761125 GCTTAAAGTAGAGGAACAAAAAGAAGAACAGAAGGAGTTAGAGAAATCTGAAAAAGAAGAGGATG GCTTAAAGTAGAGGAACAAAAAGAAGAACAGACGGAGTTAGAGAAATCTGAAAAAGAAGAGGATG A C CCAR1 Ensembl:ENSG00000060339 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68761076..68761223 26863196 MeRIP-seq:(Medium) rs772492295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26173,Human_RBP_ID_1769432,Human_RBP_ID_3355104,Human_RBP_ID_4142682,Human_RBP_ID_5545745,Human_RBP_ID_5990999,Human_RBP_ID_9343566,Human_RBP_ID_18525074,Human_RBP_ID_22886737,Human_RBP_ID_23112911,Human_RBP_ID_23464588,Human_RBP_ID_24541974 Human_Splice_Rec_1139683,Human_Splice_Rec_1139737,Human_Splice_Rec_1139783,Human_Splice_Rec_1139811,Human_Splice_Rec_1139841,Human_Splice_Rec_1139883,Human_Splice_Rec_1139925,Human_Splice_Rec_1139953,Human_Splice_Rec_1139989,Human_Splice_Rec_1140017,Human_Splice_Rec_1140021,Human_Splice_Rec_1140031 RMVar_hsa_circ_14730,RMVar_hsa_circ_356781,RMVar_hsa_circ_307164,RMVar_hsa_circ_37797,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_115064,RMVar_hsa_circ_143889,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_6320,RMVar_hsa_circ_269541,RMVar_hsa_circ_29756,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901,RMVar_hsa_circ_280012,RMVar_hsa_circ_326290,RMVar_hsa_circ_276902,RMVar_hsa_circ_143904,RMVar_hsa_circ_268652,RMVar_hsa_circ_143905,RMVar_hsa_circ_143906,RMVar_hsa_circ_368301,RMVar_hsa_circ_311164,RMVar_hsa_circ_38883,RMVar_hsa_circ_289248,RMVar_hsa_circ_52772,RMVar_hsa_circ_308624,RMVar_hsa_circ_339094,RMVar_hsa_circ_353284,RMVar_hsa_circ_334686,RMVar_hsa_circ_143908,RMVar_hsa_circ_143909 78625 RMVar_ID_78625 Human_SNP_ID_436542899 m1A Human chr10 + 68773038 68773038 68773038 GATGATTCTAAAGATGATGATGAAACTGAAGAAGATAACAATCAAGATGAATATGACCCTATGGA GATGATTCTAAAGATGATGATGAAACTGAAGACGATAACAATCAAGATGAATATGACCCTATGGA A C CCAR1 Ensembl:ENSG00000060339 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68772926..68773162 26863196 MeRIP-seq:(Medium) rs1409425790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26179,Human_RBP_ID_1448854,Human_RBP_ID_1769454,Human_RBP_ID_2228197,Human_RBP_ID_5991079,Human_RBP_ID_8762446,Human_RBP_ID_9343399,Human_RBP_ID_9360407,Human_RBP_ID_17227850,Human_RBP_ID_17344444,Human_RBP_ID_17460541,Human_RBP_ID_18410386,Human_RBP_ID_18525080,Human_RBP_ID_18596709,Human_RBP_ID_21964744,Human_RBP_ID_23481229,Human_RBP_ID_24541982,Human_RBP_ID_26316361,Human_RBP_ID_27194241,Human_RBP_ID_27802105 Human_Splice_Rec_1139688,Human_Splice_Rec_1139689,Human_Splice_Rec_1139742,Human_Splice_Rec_1139743,Human_Splice_Rec_1139846,Human_Splice_Rec_1139847,Human_Splice_Rec_1139888,Human_Splice_Rec_1139889,Human_Splice_Rec_1139994,Human_Splice_Rec_1139995,Human_Splice_Rec_1140024,Human_Splice_Rec_1140025,Human_Splice_Rec_1140035 RMVar_hsa_circ_307164,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_115064,RMVar_hsa_circ_143889,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_337764,RMVar_hsa_circ_6320,RMVar_hsa_circ_29756,RMVar_hsa_circ_317570,RMVar_hsa_circ_143901,RMVar_hsa_circ_280012,RMVar_hsa_circ_276902,RMVar_hsa_circ_143904,RMVar_hsa_circ_268652,RMVar_hsa_circ_143905,RMVar_hsa_circ_143906,RMVar_hsa_circ_368301,RMVar_hsa_circ_311164,RMVar_hsa_circ_38883,RMVar_hsa_circ_1296,RMVar_hsa_circ_289248,RMVar_hsa_circ_308624,RMVar_hsa_circ_334686,RMVar_hsa_circ_143908,RMVar_hsa_circ_143909,RMVar_hsa_circ_355245,RMVar_hsa_circ_71115,RMVar_hsa_circ_298943,RMVar_hsa_circ_27926,RMVar_hsa_circ_328433,RMVar_hsa_circ_143912,RMVar_hsa_circ_69537,RMVar_hsa_circ_143911 78626 RMVar_ID_78626 Human_SNP_ID_436546455 m1A Human chr10 + 68786190 68786190 68786190 CAAACGAGATGACAAAAGAGATATCAACAGATACTGCAAGGAGAGGCCCTCTAAAGATAAGGTGT CAAACGAGATGACAAAAGAGATATCAACAGATGCTGCAAGGAGAGGCCCTCTAAAGATAAGGTGT A G CCAR1 Ensembl:ENSG00000060339 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:68786093..68786225;chr10:68786068..68786225 26863196 MeRIP-seq:(Medium) rs755031358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862394,Human_RBP_ID_1452969,Human_RBP_ID_1769471,Human_RBP_ID_2228248,Human_RBP_ID_3938276,Human_RBP_ID_5991178,Human_RBP_ID_9360410,Human_RBP_ID_17780935,Human_RBP_ID_18410338,Human_RBP_ID_19575463,Human_RBP_ID_21964746,Human_RBP_ID_22029320,Human_RBP_ID_23481230,Human_RBP_ID_24541984,Human_RBP_ID_26315934,Human_RBP_ID_27802108 Human_Splice_Rec_1139690,Human_Splice_Rec_1139691,Human_Splice_Rec_1139744,Human_Splice_Rec_1139745,Human_Splice_Rec_1139848,Human_Splice_Rec_1139849,Human_Splice_Rec_1139890,Human_Splice_Rec_1139891,Human_Splice_Rec_1139996,Human_Splice_Rec_1139997,Human_Splice_Rec_1140026,Human_Splice_Rec_1140027,Human_Splice_Rec_1140036,Human_Splice_Rec_1140037 RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_115064,RMVar_hsa_circ_143889,RMVar_hsa_circ_143888,RMVar_hsa_circ_6320,RMVar_hsa_circ_276902,RMVar_hsa_circ_268652,RMVar_hsa_circ_143905,RMVar_hsa_circ_143906,RMVar_hsa_circ_289248,RMVar_hsa_circ_143909,RMVar_hsa_circ_71115,RMVar_hsa_circ_27926,RMVar_hsa_circ_328433,RMVar_hsa_circ_143912,RMVar_hsa_circ_69537,RMVar_hsa_circ_143913,RMVar_hsa_circ_143915,RMVar_hsa_circ_272077,RMVar_hsa_circ_292950,RMVar_hsa_circ_302701,RMVar_hsa_circ_48252,RMVar_hsa_circ_143914 78627 RMVar_ID_78627 Human_SNP_ID_436575706 m1A Human chr10 - 68901356 68901356 68901356 GCATTACTGGCCACCGCCGCCTCCCTCCGGGCACAGTGGCCACAACCACCTACGGGCAGCGACAG GCATTACTGGCCACCGCCGCCTCCCTCCGGGCCCAGTGGCCACAACCACCTACGGGCAGCGACAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68901310..68906231 26863196 MeRIP-seq:(Medium) rs1465516224 Functional Loss SNV dbSNP153 33..33 33 - - - 78628 RMVar_ID_78628 Human_SNP_ID_436575712 m1A Human chr10 + 68901367 68901367 68901367 CGTAGGTGGTTGTGGCCACTGTGCCCGGAGGGAGGCGGCGGTGGCCAGTAATGCCTGGGAAACTC CGTAGGTGGTTGTGGCCACTGTGCCCGGAGGGGGGCGGCGGTGGCCAGTAATGCCTGGGAAACTC A G DDX50 Ensembl:ENSG00000107625 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:68901321..68901464 26863196 MeRIP-seq:(Medium) rs1013880990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136301,Human_RBP_ID_8765320,Human_RBP_ID_9320574,Human_RBP_ID_18416122,Human_RBP_ID_18431899 78629 RMVar_ID_78629 Human_SNP_ID_436575732 m1A Human chr10 - 68901401 68901401 68901401 AGGGTGCTTCCAGCTCCATAATGTCCCCCCAGAGGAGTTTCCCAGGCATTACTGGCCACCGCCGC AGGGTGCTTCCAGCTCCATAATGTCCCCCCAGGGGAGTTTCCCAGGCATTACTGGCCACCGCCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:68901376..68901400 32194978 MeRIP-seq:(Medium) rs149537865 Functional Loss SNV dbSNP153 33..33 33 - - - 78630 RMVar_ID_78630 Human_SNP_ID_436575771 m1A Human chr10 - 68901473 68901473 68901473 GCCCAAAAGGAGGCGCGGCCCATGCTCAGCGCACCTTTTGCCTCTCCTTCTTCTGGCTCTCGGAC GCCCAAAAGGAGGCGCGGCCCATGCTCAGCGCTCCTTTTGCCTCTCCTTCTTCTGGCTCTCGGAC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:68901426..68906850 32194978 MeRIP-seq:(Medium) rs1424058918 Functional Loss SNV dbSNP153 33..33 33 - - - 78631 RMVar_ID_78631 Human_SNP_ID_436578321 m1A Human chr10 + 68911120 68911120 68911120 TTTCCTATTCAAGTTAAGACCTTTGGTCCTGTATATGAAGGAAAAGATTTAATAGCTCAAGCACG TTTCCTATTCAAGTTAAGACCTTTGGTCCTGTGTATGAAGGAAAAGATTTAATAGCTCAAGCACG A G DDX50 Ensembl:ENSG00000107625 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:68910351..68911136 32194978 MeRIP-seq:(Medium) rs113058356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18596763,Human_RBP_ID_27194251 Human_Splice_Rec_1140082,Human_Splice_Rec_1140092,Human_Splice_Rec_1140118,Human_Splice_Rec_1140148 RMVar_hsa_circ_368843,RMVar_hsa_circ_318620,RMVar_hsa_circ_322434,RMVar_hsa_circ_47167,RMVar_hsa_circ_16645,RMVar_hsa_circ_300143,RMVar_hsa_circ_42255,RMVar_hsa_circ_311489,RMVar_hsa_circ_340223,RMVar_hsa_circ_331697,RMVar_hsa_circ_44208,RMVar_hsa_circ_143924,RMVar_hsa_circ_312450,RMVar_hsa_circ_97195,RMVar_hsa_circ_125543,RMVar_hsa_circ_26000,RMVar_hsa_circ_143926,RMVar_hsa_circ_143927,RMVar_hsa_circ_143928,RMVar_hsa_circ_143925 78632 RMVar_ID_78632 Human_SNP_ID_436587599 m1A Human chr10 + 68946558 68946558 68946558 CAGAGTCGACAAGGAAGTCGCTCAGGAAGTCGACAAGATGGTAGAAGACGAAGTGGGAATAGAAA CAGAGTCGACAAGGAAGTCGCTCAGGAAGTCGCCAAGATGGTAGAAGACGAAGTGGGAATAGAAA A C DDX50 Ensembl:ENSG00000107625 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:68946447..68946700 32194978 MeRIP-seq:(Medium) rs1176987373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1769536 RMVar_hsa_circ_92087,RMVar_hsa_circ_89745,RMVar_hsa_circ_143933,RMVar_hsa_circ_143934,RMVar_hsa_circ_143935 78633 RMVar_ID_78633 Human_SNP_ID_436590008 m1A Human chr10 - 68956252 68956252 68956252 CCTTTTTTCATTGCGGTGTCTGATTCCAAACCAGCGTCACTACGGAGTTTTCCCGGCATCTTCAG CCTTTTTTCATTGCGGTGTCTGATTCCAAACCGGCGTCACTACGGAGTTTTCCCGGCATCTTCAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:68956201..68956357 26863196 MeRIP-seq:(Medium) rs775845397 Functional Loss SNV dbSNP153 33..33 33 - - - 78634 RMVar_ID_78634 Human_SNP_ID_436590030 m1A Human chr10 + 68956311 68956311 68956311 AAAAGGGGAGACACTGCGAAAGCAAACCGAGGAGGTGAAACGGAGGGACCTGGGGCCAGGAGGGA AAAAGGGGAGACACTGCGAAAGCAAACCGAGGTGGTGAAACGGAGGGACCTGGGGCCAGGAGGGA A T DDX21 Ensembl:ENSG00000165732 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:68956151..68956365;chr10:68956192..68956387;chr10:68956176..68956367;chr10:68956151..68956507;chr10:68956176..68956454 26863196 MeRIP-seq:(Medium) rs1468423605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136303,Human_RBP_ID_24542106,Human_RBP_ID_26317249,Human_RBP_ID_27802782 Human_Splice_Rec_1140167 RMVar_hsa_circ_143936 78635 RMVar_ID_78635 Human_SNP_ID_436590957 m1A Human chr10 + 68960057 68960057 68960057 GAAAAGAAAGTGGTTTCTTCTAAAACCAAAAAAGTGACAAAAAATGAGGAGCCTTCTGAGGAAGA GAAAAGAAAGTGGTTTCTTCTAAAACCAAAAACGTGACAAAAAATGAGGAGCCTTCTGAGGAAGA A C DDX21 Ensembl:ENSG00000165732 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68960007..68960139 26863196 MeRIP-seq:(Medium) rs938816389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_380535,Human_RBP_ID_1769547,Human_RBP_ID_2228353,Human_RBP_ID_3355255,Human_RBP_ID_4124303,Human_RBP_ID_8762489,Human_RBP_ID_11403347,Human_RBP_ID_17780998 RMVar_hsa_circ_114654,RMVar_hsa_circ_336465,RMVar_hsa_circ_108868,RMVar_hsa_circ_143936,RMVar_hsa_circ_347380,RMVar_hsa_circ_143937,RMVar_hsa_circ_351831,RMVar_hsa_circ_341537,RMVar_hsa_circ_292699,RMVar_hsa_circ_310409,RMVar_hsa_circ_270353,RMVar_hsa_circ_143939,RMVar_hsa_circ_143940,RMVar_hsa_circ_143941,RMVar_hsa_circ_143938 78636 RMVar_ID_78636 Human_SNP_ID_436591750 m1A Human chr10 - 68963438 68963438 68963438 CCTGAGGGGCACGGCCTCTCTTCCTGTCTTGCAGTTCCCCATGAAGTTTCTCAATCAAAGGGATG CCTGAGGGGCACGGCCTCTCTTCCTGTCTTGCGGTTCCCCATGAAGTTTCTCAATCAAAGGGATG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:68962087..68967098 32194978 MeRIP-seq:(Medium) rs1232779372 Functional Loss SNV dbSNP153 33..33 33 - - - 78637 RMVar_ID_78637 Human_SNP_ID_436595306 m1A Human chr10 - 68978958 68978958 68978958 GACCCCAGCCTTACCAGCTTTCCTTTGAGAAAAACCATTCCCTTCACTTTGGAATCAATCTCCTC GACCCCAGCCTTACCAGCTTTCCTTTGAGAAAGACCATTCCCTTCACTTTGGAATCAATCTCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:68978908..68979016 26863196 MeRIP-seq:(Medium) rs1564630281 Functional Loss SNV dbSNP153 33..33 33 - - - 78638 RMVar_ID_78638 Human_SNP_ID_436596208 m1A Human chr10 - 68982743 68982743 68982743 CCTTTGTTTTGGGATCTGTTACTTTTGTTGCCACCTCCTGATCGCTGTCCTCTCGGGCCTCTACT CCTTTGTTTTGGGATCTGTTACTTTTGTTGCCGCCTCCTGATCGCTGTCCTCTCGGGCCTCTACT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:68982526..68982775 26863196 MeRIP-seq:(Medium) rs1457590517 Functional Loss SNV dbSNP153 33..33 33 - - - 78639 RMVar_ID_78639 Human_SNP_ID_436597570 m1A Human chr10 - 68988832 68988832 68988832 TCGCAGACCTCTGCCCACGGAACGTTCGCCATAGCGGCCTCTACTGCCTGGCTTTCCTCAATGTT TCGCAGACCTCTGCCCACGGAACGTTCGCCATGGCGGCCTCTACTGCCTGGCTTTCCTCAATGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:68988776..68989239;chr10:68988776..68989217 26863196 MeRIP-seq:(Medium) rs377211706 Functional Loss SNV dbSNP153 33..33 33 - - - 78640 RMVar_ID_78640 Human_SNP_ID_436597691 m1A Human chr10 - 68989149 68989149 68989149 GCTCCTCCCCCGCCGACAGCTCCTCCGTGTCGATGTGGTTCACCCCGAGGTGGAACTCGATGACT GCTCCTCCCCCGCCGACAGCTCCTCCGTGTCGGTGTGGTTCACCCCGAGGTGGAACTCGATGACT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:68989067..68989488 26863410 MeRIP-seq:(Medium) rs912912274 Functional Loss SNV dbSNP153 33..33 33 - - - 78641 RMVar_ID_78641 Human_SNP_ID_436695358 m1A Human chr10 - 69376886 69376886 69376886 CACCGGCACTTGTCAGCCTTCCTCTGCGCCCCACACACGAGGGCTGGGACAGACATAAAAGGAAT CACCGGCACTTGTCAGCCTTCCTCTGCGCCCCCCACACGAGGGCTGGGACAGACATAAAAGGAAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:69376884..69377040 26863196 MeRIP-seq:(Medium) rs1222428174 Functional Loss SNV dbSNP153 33..33 33 - - - 78642 RMVar_ID_78642 Human_SNP_ID_436697288 m1A Human chr10 + 69384411 69384411 69384411 TGTGCTGCTGGTGAAAATCCGTAGTGGGAAAAAGAGAACGGTGGAAATGCACAACAAGATCTACG TGTGCTGCTGGTGAAAATCCGTAGTGGGAAAAGGAGAACGGTGGAAATGCACAACAAGATCTACG A G HK1 Ensembl:ENSG00000156515 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:69384361..69384511 32194978 MeRIP-seq:(Medium) rs1484874788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18187929 Human_Splice_Rec_1140640,Human_Splice_Rec_1140641,Human_Splice_Rec_1140698,Human_Splice_Rec_1140699,Human_Splice_Rec_1140740,Human_Splice_Rec_1140741,Human_Splice_Rec_1140824,Human_Splice_Rec_1140825,Human_Splice_Rec_1140886,Human_Splice_Rec_1140887,Human_Splice_Rec_1140920,Human_Splice_Rec_1140921,Human_Splice_Rec_1140954,Human_Splice_Rec_1140955,Human_Splice_Rec_1140986 RMVar_hsa_circ_116921,RMVar_hsa_circ_47729,RMVar_hsa_circ_144006,RMVar_hsa_circ_97069,RMVar_hsa_circ_144011,RMVar_hsa_circ_6788,RMVar_hsa_circ_144014,RMVar_hsa_circ_117876,RMVar_hsa_circ_144017,RMVar_hsa_circ_33216,RMVar_hsa_circ_300168,RMVar_hsa_circ_372687,RMVar_hsa_circ_64188,RMVar_hsa_circ_343162,RMVar_hsa_circ_144016,RMVar_hsa_circ_373199,RMVar_hsa_circ_337171,RMVar_hsa_circ_41688,RMVar_hsa_circ_144018 78643 RMVar_ID_78643 Human_SNP_ID_436700705 m1A Human chr10 + 69398774 69398774 69398774 TGTGGATAAGATCCGCGAGAACAGAGGACTGGACCGTCTGAATGTGACTGTGGGAGTGGACGGGA TGTGGATAAGATCCGCGAGAACAGAGGACTGGGCCGTCTGAATGTGACTGTGGGAGTGGACGGGA A G HK1 Ensembl:ENSG00000156515 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:69398626..69401335 32194978 MeRIP-seq:(Medium) rs779879396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225364,Human_RBP_ID_8765602,Human_RBP_ID_9274161,Human_RBP_ID_18188051,Human_RBP_ID_23465239 Human_Splice_Rec_1140653,Human_Splice_Rec_1140711,Human_Splice_Rec_1140753,Human_Splice_Rec_1140837,Human_Splice_Rec_1140899,Human_Splice_Rec_1140933,Human_Splice_Rec_1140967 Human_miRNA_ID_2021954,Human_miRNA_ID_2119711,Human_miRNA_ID_2122928,Human_miRNA_ID_2126143,Human_miRNA_ID_2129365,Human_miRNA_ID_2260496,Human_miRNA_ID_2263541,Human_miRNA_ID_2266610,Human_miRNA_ID_2601998,Human_miRNA_ID_3103325 RMVar_hsa_circ_97069,RMVar_hsa_circ_144011,RMVar_hsa_circ_144014,RMVar_hsa_circ_117876,RMVar_hsa_circ_64188,RMVar_hsa_circ_144020,RMVar_hsa_circ_295801,RMVar_hsa_circ_95354,RMVar_hsa_circ_144019,RMVar_hsa_circ_114125,RMVar_hsa_circ_144021,RMVar_hsa_circ_11599,RMVar_hsa_circ_320109 78644 RMVar_ID_78644 Human_SNP_ID_436758249 m1A Human chr10 + 69630292 69630292 69630292 CCGCCTGGAGCCGCCGGGAGTGGACGCCGCCGAGGCCCGGAGTCGCGCCTGCAGGTGAGTCGCCG CCGCCTGGAGCCGCCGGGAGTGGACGCCGCCGTGGCCCGGAGTCGCGCCTGCAGGTGAGTCGCCG A T FAM241B Ensembl:ENSG00000171224 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:69630284..69630446 26863196 MeRIP-seq:(Medium) rs908964540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1141087,Human_Splice_Rec_1141093 78645 RMVar_ID_78645 Human_SNP_ID_436801451 m1A Human chr10 + 69802623 69802597 69802624 ACTCAGCCTGCTCGCCCACTTTCGGACGGCCGAGCTGCAGGCCCGGGTGCTGCGCCTGGAAGCGG ACTCAGC___________________________CTGCAGGCCCGGGTGCTGCGCCTGGAAGCGG CCTGCTCGCCCACTTTCGGACGGCCGAG C COL13A1 Ensembl:ENSG00000197467 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:69802526..69822376 32194978 MeRIP-seq:(Medium) rs767174029 Functional Loss DEL dbSNP153 8..34 33 - - - Human_Splice_Rec_1141109,Human_Splice_Rec_1141189,Human_Splice_Rec_1141263,Human_Splice_Rec_1141341,Human_Splice_Rec_1141347,Human_Splice_Rec_1141427,Human_Splice_Rec_1141503,Human_Splice_Rec_1141569,Human_Splice_Rec_1141639,Human_Splice_Rec_1141707,Human_Splice_Rec_1141771,Human_Splice_Rec_1141843,Human_Splice_Rec_1141917,Human_Splice_Rec_1141983,Human_Splice_Rec_1142059,Human_Splice_Rec_1142127,Human_Splice_Rec_1142199,Human_Splice_Rec_1142269,Human_Splice_Rec_1142317,Human_Splice_Rec_1142389 78646 RMVar_ID_78646 Human_SNP_ID_436831895 m1A Human chr10 + 69924992 69924992 69924992 CAGGGGGAGCGTGGAGCAGCTGGAGAACAGGGACCAGATGGCCCCAAGGTATGTGCCTCTCCCTC CAGGGGGAGCGTGGAGCAGCTGGAGAACAGGGGCCAGATGGCCCCAAGGTATGTGCCTCTCCCTC A G COL13A1 Ensembl:ENSG00000197467 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:69923837..69925840 32194978 MeRIP-seq:(Medium) rs1342795509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1141156,Human_Splice_Rec_1141157,Human_Splice_Rec_1141234,Human_Splice_Rec_1141235,Human_Splice_Rec_1141308,Human_Splice_Rec_1141309,Human_Splice_Rec_1141394,Human_Splice_Rec_1141395,Human_Splice_Rec_1141470,Human_Splice_Rec_1141471,Human_Splice_Rec_1141540,Human_Splice_Rec_1141541,Human_Splice_Rec_1141612,Human_Splice_Rec_1141613,Human_Splice_Rec_1141676,Human_Splice_Rec_1141677,Human_Splice_Rec_1141740,Human_Splice_Rec_1141741,Human_Splice_Rec_1141814,Human_Splice_Rec_1141815,Human_Splice_Rec_1141886,Human_Splice_Rec_1141887,Human_Splice_Rec_1141956,Human_Splice_Rec_1141957,Human_Splice_Rec_1142028,Human_Splice_Rec_1142029,Human_Splice_Rec_1142098,Human_Splice_Rec_1142099,Human_Splice_Rec_1142170,Human_Splice_Rec_1142171,Human_Splice_Rec_1142242,Human_Splice_Rec_1142243,Human_Splice_Rec_1142308,Human_Splice_Rec_1142309,Human_Splice_Rec_1142360,Human_Splice_Rec_1142361,Human_Splice_Rec_1142434,Human_Splice_Rec_1142435,Human_Splice_Rec_1142504,Human_Splice_Rec_1142505,Human_Splice_Rec_1142558,Human_Splice_Rec_1142559,Human_Splice_Rec_1142596,Human_Splice_Rec_1142597,Human_Splice_Rec_1142630,Human_Splice_Rec_1142631 RMVar_hsa_circ_144027,RMVar_hsa_circ_95504,RMVar_hsa_circ_107823,RMVar_hsa_circ_80123,RMVar_hsa_circ_144028,RMVar_hsa_circ_52585,RMVar_hsa_circ_144026,RMVar_hsa_circ_335905,RMVar_hsa_circ_144029,RMVar_hsa_circ_269073 78647 RMVar_ID_78647 Human_SNP_ID_436877244 m1A Human chr10 - 70120552 70120552 70120552 TTCATCGTGGTGGTGGGAGGAGGCTCGGCTGGAGTGGAGATGGCAGCAGAGATTAAAACAGAATA TTCATCGTGGTGGTGGGAGGAGGCTCGGCTGGGGTGGAGATGGCAGCAGAGATTAAAACAGAATA T C AIFM2 Ensembl:ENSG00000042286 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:70120501..70120632 26863196 MeRIP-seq:(Medium) rs753480972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26073,Human_RBP_ID_746975,Human_RBP_ID_804975,Human_RBP_ID_862408,Human_RBP_ID_5340501 Human_Splice_Rec_1142852,Human_Splice_Rec_1142853,Human_Splice_Rec_1142870,Human_Splice_Rec_1142871,Human_Splice_Rec_1142886,Human_Splice_Rec_1142887 RMVar_hsa_circ_144031,RMVar_hsa_circ_144030,RMVar_hsa_circ_6924,RMVar_hsa_circ_87597,RMVar_hsa_circ_144037,RMVar_hsa_circ_144036,RMVar_hsa_circ_57785,RMVar_hsa_circ_144038,RMVar_hsa_circ_57683 78648 RMVar_ID_78648 Human_SNP_ID_436878104 m1A Human chr10 - 70123479 70123479 70123479 AAAAGACATTCATTTCTTACTCGGTGACTTTCAAGGACAACTTCCGGCAGGGGCTAGTAGTGGGG AAAAGACATTCATTTCTTACTCGGTGACTTTCCAGGACAACTTCCGGCAGGGGCTAGTAGTGGGG T G AIFM2 Ensembl:ENSG00000042286 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:70120533..70132735 32194978 MeRIP-seq:(Medium) rs777858004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862410 Human_Splice_Rec_1142848,Human_Splice_Rec_1142849,Human_Splice_Rec_1142866,Human_Splice_Rec_1142867,Human_Splice_Rec_1142882,Human_Splice_Rec_1142883 RMVar_hsa_circ_144031,RMVar_hsa_circ_144030,RMVar_hsa_circ_6924,RMVar_hsa_circ_144037,RMVar_hsa_circ_144036,RMVar_hsa_circ_33229,RMVar_hsa_circ_57785,RMVar_hsa_circ_57683,RMVar_hsa_circ_23440 78649 RMVar_ID_78649 Human_SNP_ID_436880211 m1A Human chr10 - 70132761 70132761 70132761 CAAGCGGGAGCGGGAGCGGGAGCGGGAGCCGGAGCGAGAGCGCGCGGGCGCGGCCGACAGGTGAG CAAGCGGGAGCGGGAGCGGGAGCGGGAGCCGGGGCGAGAGCGCGCGGGCGCGGCCGACAGGTGAG T C AIFM2 Ensembl:ENSG00000042286 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:70123951..70132850;chr10:70123374..70132889;chr10:70123467..70132878 26863196 MeRIP-seq:(Medium) rs1163813309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748390,Human_RBP_ID_805144,Human_RBP_ID_4135854,Human_RBP_ID_5313018,Human_RBP_ID_18416124,Human_RBP_ID_19046593,Human_RBP_ID_22431700,Human_RBP_ID_22886885 Human_Splice_Rec_1142863,Human_Splice_Rec_1142879 78650 RMVar_ID_78650 Human_SNP_ID_436884057 m1A Human chr10 + 70146174 70146172 70146175 GCGCGAAGTGGGCCCAGAAGGCCGGGCAGCTCAGCAGCAGCAGCAGCTCAGCAGGAAGCCGGGGC GCGCGAAGTGGGCCCAGAAGGCCGGGCAGCT___CAGCAGCAGCAGCTCAGCAGGAAGCCGGGGC TCAG T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:70146125..70146226 32194978 MeRIP-seq:(Medium) rs746237835 Functional Loss DEL dbSNP153 32..34 33 - - - 78651 RMVar_ID_78651 Human_SNP_ID_436884188 m1A Human chr10 + 70146426 70146426 70146426 TCAGGACTTCGCTGCCAGCTCGCAGGAAGGGGACGAAGATGCCCCCGTGGCAAAGCACCAGGCCC TCAGGACTTCGCTGCCAGCTCGCAGGAAGGGGGCGAAGATGCCCCCGTGGCAAAGCACCAGGCCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:70146325..70146426 26863410 MeRIP-seq:(Medium) rs756895428 Functional Loss SNV dbSNP153 33..33 33 - - - 78652 RMVar_ID_78652 Human_SNP_ID_436884227 m1A Human chr10 - 70146512 70146512 70146512 GCGGGCTGCATGGTGAGCGCCTCCCGGGCCGGACAGCCCGAGGCGGGCCCGTGGAGCTGCAGCGG GCGGGCTGCATGGTGAGCGCCTCCCGGGCCGGGCAGCCCGAGGCGGGCCCGTGGAGCTGCAGCGG T C TYSND1 Ensembl:ENSG00000156521 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:70146464..70146650 26863196 MeRIP-seq:(Medium) rs999277056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4125141,Human_RBP_ID_19537778 78653 RMVar_ID_78653 Human_SNP_ID_436884237 m1A Human chr10 + 70146531 70146531 70146531 CCGCCTCGGGCTGTCCGGCCCGGGAGGCGCTCACCATGCAGCCCGCCTGCTCGGCCGCCCTCATG CCGCCTCGGGCTGTCCGGCCCGGGAGGCGCTCCCCATGCAGCCCGCCTGCTCGGCCGCCCTCATG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:70146525..70146626 26863410 MeRIP-seq:(Medium) rs750050724 Functional Loss SNV dbSNP153 33..33 33 - - - 78654 RMVar_ID_78654 Human_SNP_ID_436890198 m1A Human chr10 + 70170439 70170413 70170439 ACTCACGGCCTGAGGGGCTCCTCCGGCAAAACAGCGGCTGGCTCGGACCCTCCCTCAGAGCACAC ACTCACG__________________________GCGGCTGGCTCGGACCCTCCCTCAGAGCACAC GGCCTGAGGGGCTCCTCCGGCAAAACA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:70170423..70170523 32194978 MeRIP-seq:(Medium) rs1439228895 Functional Loss DEL dbSNP153 8..33 33 - - - 78655 RMVar_ID_78655 Human_SNP_ID_436901435 m1A Human chr10 - 70217933 70217933 70217933 AAATATGCAAAGATTTGAAATTTTCTTATTTCAGATTGCTACAAAGGACCCTTTAAACCCTATTA AAATATGCAAAGATTTGAAATTTTCTTATTTCGGATTGCTACAAAGGACCCTTTAAACCCTATTA T C PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:70217901..70217950 26863196 MeRIP-seq:(Medium) rs775918409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11407606,Human_RBP_ID_17787080 RMVar_hsa_circ_144049,RMVar_hsa_circ_114183,RMVar_hsa_circ_144050,RMVar_hsa_circ_91617,RMVar_hsa_circ_378296,RMVar_hsa_circ_144057,RMVar_hsa_circ_144058,RMVar_hsa_circ_346134,RMVar_hsa_circ_144060,RMVar_hsa_circ_280611,RMVar_hsa_circ_144064,RMVar_hsa_circ_272487,RMVar_hsa_circ_144066,RMVar_hsa_circ_118844,RMVar_hsa_circ_144067,RMVar_hsa_circ_310480 78656 RMVar_ID_78656 Human_SNP_ID_436901622 m1A Human chr10 - 70218778 70218778 70218778 TTCACATGGTAGTTGAAGTACCACGCTGGTCTAATGCAAAAATGGAGGTAATATTTCACCTTACA TTCACATGGTAGTTGAAGTACCACGCTGGTCTCATGCAAAAATGGAGGTAATATTTCACCTTACA T G PPA1 Ensembl:ENSG00000180817 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:70218776..70218825 26863196 MeRIP-seq:(Medium) rs778475473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_381074,Human_RBP_ID_1769849,Human_RBP_ID_4142994,Human_RBP_ID_8991558,Human_RBP_ID_17229326,Human_RBP_ID_17680496,Human_RBP_ID_17787082,Human_RBP_ID_19046601,Human_RBP_ID_23206646,Human_RBP_ID_23465827,Human_RBP_ID_26802002,Human_RBP_ID_26881339,Human_RBP_ID_27194488 Human_Splice_Rec_1142992,Human_Splice_Rec_1142993,Human_Splice_Rec_1143016,Human_Splice_Rec_1143017,Human_Splice_Rec_1143030,Human_Splice_Rec_1143031,Human_Splice_Rec_1143040,Human_Splice_Rec_1143044 Human_miRNA_ID_2005127 RMVar_hsa_circ_144049,RMVar_hsa_circ_114183,RMVar_hsa_circ_144050,RMVar_hsa_circ_91617,RMVar_hsa_circ_378296,RMVar_hsa_circ_144057,RMVar_hsa_circ_144058,RMVar_hsa_circ_346134,RMVar_hsa_circ_144060,RMVar_hsa_circ_280611,RMVar_hsa_circ_144064,RMVar_hsa_circ_272487,RMVar_hsa_circ_144066,RMVar_hsa_circ_118844,RMVar_hsa_circ_144067,RMVar_hsa_circ_310480 78657 RMVar_ID_78657 Human_SNP_ID_436905781 m1A Human chr10 - 70233341 70233341 70233341 CGGGCTGGTGGCTCTGTGGCAGCGGCGGCGGCAGGACTCCGGCACTATGAGCGGCTTCAGCACCG CGGGCTGGTGGCTCTGTGGCAGCGGCGGCGGCGGGACTCCGGCACTATGAGCGGCTTCAGCACCG T C PPA1 Ensembl:ENSG00000180817 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:70230351..70233425;chr10:70233215..70233425 26863196 MeRIP-seq:(Medium) rs1021440152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225978,Human_RBP_ID_381088,Human_RBP_ID_748607,Human_RBP_ID_4136319,Human_RBP_ID_8762725,Human_RBP_ID_9274163,Human_RBP_ID_9320587,Human_RBP_ID_11407909,Human_RBP_ID_23123784,Human_RBP_ID_23206431,Human_RBP_ID_26881343 Human_Splice_Rec_1142989,Human_Splice_Rec_1143013,Human_Splice_Rec_1143027 78658 RMVar_ID_78658 Human_SNP_ID_436905797 m1A Human chr10 - 70233353 70233353 70233353 CGGCGCCGCGTGCGGGCTGGTGGCTCTGTGGCAGCGGCGGCGGCAGGACTCCGGCACTATGAGCG CGGCGCCGCGTGCGGGCTGGTGGCTCTGTGGCGGCGGCGGCGGCAGGACTCCGGCACTATGAGCG T C PPA1 Ensembl:ENSG00000180817 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:70230326..70233419 26863196 MeRIP-seq:(Medium) rs1564587760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225978,Human_RBP_ID_381088,Human_RBP_ID_748607,Human_RBP_ID_4136319,Human_RBP_ID_9274163,Human_RBP_ID_9320587,Human_RBP_ID_11407910,Human_RBP_ID_17781339,Human_RBP_ID_22788558,Human_RBP_ID_23206431,Human_RBP_ID_23465848,Human_RBP_ID_27194495 Human_Splice_Rec_1142989,Human_Splice_Rec_1143013,Human_Splice_Rec_1143027 78659 RMVar_ID_78659 Human_SNP_ID_436905799 m1A Human chr10 + 70233359 70233359 70233359 TAGTGCCGGAGTCCTGCCGCCGCCGCTGCCACAGAGCCACCAGCCCGCACGCGGCGCCGACTGAC TAGTGCCGGAGTCCTGCCGCCGCCGCTGCCACGGAGCCACCAGCCCGCACGCGGCGCCGACTGAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:70233251..70233425 26863410 MeRIP-seq:(Medium) rs970633434 Functional Loss SNV dbSNP153 33..33 33 - - - 78660 RMVar_ID_78660 Human_SNP_ID_436905805 m1A Human chr10 + 70233368 70233368 70233368 AGTCCTGCCGCCGCCGCTGCCACAGAGCCACCAGCCCGCACGCGGCGCCGACTGACAAGGAGAGA AGTCCTGCCGCCGCCGCTGCCACAGAGCCACCGGCCCGCACGCGGCGCCGACTGACAAGGAGAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:70233251..70233425 26863196 MeRIP-seq:(Medium) rs1418695504 Functional Loss SNV dbSNP153 33..33 33 - - - 78661 RMVar_ID_78661 Human_SNP_ID_436948446 m1A Human chr10 + 70404276 70404275 70404276 AGGGCGGCGGCGGGAGCGGAGCGGGACGAGGGAACGGGAGGAAGCGAGCGAGGAGCGCGCAGAGC AGGGCGGCGGCGGGAGCGGAGCGGGACGAGGG_ACGGGAGGAAGCGAGCGAGGAGCGCGCAGAGC GA G EIF4EBP2 Ensembl:ENSG00000148730 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:70404226..70404375 26863196 MeRIP-seq:(Medium) rs1236034857 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_2959046 RMVar_hsa_circ_98215,RMVar_hsa_circ_144070 78662 RMVar_ID_78662 Human_SNP_ID_436948510 m1A Human chr10 + 70404402 70404402 70404402 CCGGACAAAGCCGAGAGCCCGCGCCCACAGCCATGTCCTCGTCAGCCGGCAGCGGCCACCAGCCC CCGGACAAAGCCGAGAGCCCGCGCCCACAGCCCTGTCCTCGTCAGCCGGCAGCGGCCACCAGCCC A C EIF4EBP2 Ensembl:ENSG00000148730 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:70404151..70404550 26863410 MeRIP-seq:(Medium) rs763404768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4143014,Human_RBP_ID_22029813,Human_RBP_ID_27194561 RMVar_hsa_circ_98215,RMVar_hsa_circ_144070 78663 RMVar_ID_78663 Human_SNP_ID_436953556 m1A Human chr10 + 70422031 70422031 70422031 GAGCTAAGCAGCCCTTAGAGGAAAACAGTTCAACTCTGACTTTCCTAGTTGTTTTTTTATTGAGA GAGCTAAGCAGCCCTTAGAGGAAAACAGTTCAGCTCTGACTTTCCTAGTTGTTTTTTTATTGAGA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1304764760 Functional Loss SNV dbSNP153 33..33 33 - - - 78664 RMVar_ID_78664 Human_SNP_ID_437055113 m1A Human chr10 + 70816095 70816095 70816095 CAGGAGGTGGAGCCGGCCGGGTGCTCGAGGGAAGGAGACTGGAAGCTGGTTCCGGCGTGAGGAGG CAGGAGGTGGAGCCGGCCGGGTGCTCGAGGGAGGGAGACTGGAAGCTGGTTCCGGCGTGAGGAGG A G SGPL1 Ensembl:ENSG00000166224 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:70815951..70816845 26863196 MeRIP-seq:(Medium) rs1405557682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225435,Human_RBP_ID_864071,Human_RBP_ID_4136322,Human_RBP_ID_5340509,Human_RBP_ID_9352590,Human_RBP_ID_23117810,Human_RBP_ID_23466323 Human_Splice_Rec_1143289,Human_Splice_Rec_1143317 RMVar_hsa_circ_118306,RMVar_hsa_circ_144089 78665 RMVar_ID_78665 Human_SNP_ID_437055186 m1A Human chr10 - 70816335 70816335 70816335 CCCGCGGCAGGCGTGGGCTCCAGACCCGCCCCACCGCGGCCCCGCGCCCGCCCGCCGTCCACTTG CCCGCGGCAGGCGTGGGCTCCAGACCCGCCCCCCCGCGGCCCCGCGCCCGCCCGCCGTCCACTTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:70816317..70816490 26863196 MeRIP-seq:(Medium) rs1364204889 Functional Loss SNV dbSNP153 33..33 33 - - - 78666 RMVar_ID_78666 Human_SNP_ID_437072102 m1A Human chr10 - 70888483 70888483 70888483 CGCGGCCGCGATCGGGGCAGCGGGGCCGGGGCAGCCGCGGGCGAGGTGGGAGCGGGAAGGGGCGG CGCGGCCGCGATCGGGGCAGCGGGGCCGGGGCCGCCGCGGGCGAGGTGGGAGCGGGAAGGGGCGG T G PCBD1 Ensembl:ENSG00000166228 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:70888476..70888552 26863196 MeRIP-seq:(Medium) rs1251797232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416127 RMVar_hsa_circ_118733,RMVar_hsa_circ_144102 78667 RMVar_ID_78667 Human_SNP_ID_437153016 m1A Human chr10 + 71212633 71212633 71212633 GCCGGAGCCGCACGCAGCCGCGGGGCTCCGAGAGGCGCGCACTGGGGCTGGGACTGCGCGGCGCC GCCGGAGCCGCACGCAGCCGCGGGGCTCCGAGGGGCGCGCACTGGGGCTGGGACTGCGCGGCGCC A G UNC5B Ensembl:ENSG00000107731 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:71212589..71212757 26863196 MeRIP-seq:(Medium) rs1305009320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136329,Human_RBP_ID_17668479 78668 RMVar_ID_78668 Human_SNP_ID_437288002 m1A Human chr10 + 71750385 71750385 71750385 TTCATACTCAGAAGTGTCCCAGGGTGGACAAGACATTGTGTGGCACCCTTGCAATGGCCCGCGCT TTCATACTCAGAAGTGTCCCAGGGTGGACAAGCCATTGTGTGGCACCCTTGCAATGGCCCGCGCT A C CDH23 Ensembl:ENSG00000107736 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:71750296..71750396 32194978 MeRIP-seq:(Medium) rs1234842060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144108,RMVar_hsa_circ_116767 78669 RMVar_ID_78669 Human_SNP_ID_437307083 m1A Human chr10 - 71817460 71817460 71817460 TCCTCTCTCCTACCAGGCTGTCGAGCATTGCAAACGCCATGTGTGGAACTAGGAGGAGGAATATT TCCTCTCTCCTACCAGGCTGTCGAGCATTGCAGACGCCATGTGTGGAACTAGGAGGAGGAATATT T C PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:71817149..71817502 26863196 MeRIP-seq:(Medium) rs754577718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28241,Human_RBP_ID_381626,Human_RBP_ID_1770034,Human_RBP_ID_3356005,Human_RBP_ID_5994964,Human_RBP_ID_8338171,Human_RBP_ID_8991767,Human_RBP_ID_22752410,Human_RBP_ID_23467145,Human_RBP_ID_26396381 Human_Splice_Rec_1144484,Human_Splice_Rec_1144498,Human_Splice_Rec_1144522 Human_miRNA_ID_2645230 RMVar_hsa_circ_85697,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_91301,RMVar_hsa_circ_100972,RMVar_hsa_circ_88171,RMVar_hsa_circ_144117,RMVar_hsa_circ_144121,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144123,RMVar_hsa_circ_81755,RMVar_hsa_circ_144124,RMVar_hsa_circ_144122,RMVar_hsa_circ_144119,RMVar_hsa_circ_144120,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114 78670 RMVar_ID_78670 Human_SNP_ID_437307551 m1A Human chr10 + 71819029 71819029 71819029 GCCCGAGAGGACCACACCACCCAGTGAGGCTCACCAAGCACACGAAGGAAGGATCCATCACCTCC GCCCGAGAGGACCACACCACCCAGTGAGGCTCTCCAAGCACACGAAGGAAGGATCCATCACCTCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:71819026..71819125 32194978 MeRIP-seq:(Medium) rs113790176 Functional Loss SNV dbSNP153 33..33 33 - - - 78671 RMVar_ID_78671 Human_SNP_ID_437307869 m1A Human chr10 + 71819824 71819824 71819824 GGATGGACAGGATGGAGCTGCCGTACGTGTCCACCACCTCCTGGCACTCTTCCGACAGGGACTTC GGATGGACAGGATGGAGCTGCCGTACGTGTCCGCCACCTCCTGGCACTCTTCCGACAGGGACTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:71819775..71819917 26863196 MeRIP-seq:(Medium) rs763947776 Functional Loss SNV dbSNP153 33..33 33 - - - 78672 RMVar_ID_78672 Human_SNP_ID_437307904 m1A Human chr10 - 71819876 71819876 71819876 TGTTTCAGAAAGAAATACTCGACGCTTTTGACAAAATGTGCTCGAAGCTGCCGAAGTCCCTGTCG TGTTTCAGAAAGAAATACTCGACGCTTTTGACGAAATGTGCTCGAAGCTGCCGAAGTCCCTGTCG T C PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:71819826..71819925 32194978 MeRIP-seq:(Medium) rs767439180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_104261,Human_RBP_ID_1159692,Human_RBP_ID_4126167,Human_RBP_ID_8762908,Human_RBP_ID_9273301,Human_RBP_ID_23467164 Human_Splice_Rec_1144476,Human_Splice_Rec_1144514,Human_Splice_Rec_1144528,Human_Splice_Rec_1144538 RMVar_hsa_circ_124965,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_91301,RMVar_hsa_circ_100972,RMVar_hsa_circ_144117,RMVar_hsa_circ_144121,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144119,RMVar_hsa_circ_144120,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114,RMVar_hsa_circ_56643,RMVar_hsa_circ_106163,RMVar_hsa_circ_113779,RMVar_hsa_circ_144126,RMVar_hsa_circ_118638,RMVar_hsa_circ_144125,RMVar_hsa_circ_109871,RMVar_hsa_circ_144129,RMVar_hsa_circ_94744,RMVar_hsa_circ_144131,RMVar_hsa_circ_91252,RMVar_hsa_circ_144130,RMVar_hsa_circ_144127,RMVar_hsa_circ_144128,RMVar_hsa_circ_98551,RMVar_hsa_circ_373264,RMVar_hsa_circ_77099,RMVar_hsa_circ_144133,RMVar_hsa_circ_144134,RMVar_hsa_circ_340945,RMVar_hsa_circ_144135,RMVar_hsa_circ_144136,RMVar_hsa_circ_144137 78673 RMVar_ID_78673 Human_SNP_ID_437308070 m1A Human chr10 - 71820331 71820331 71820331 AAGTACTCTCCTTCTACTCTTTCCACAGAAGCACGAGGTCCCAGCAAAGTCTGATGTTTACTGTG AAGTACTCTCCTTCTACTCTTTCCACAGAAGCGCGAGGTCCCAGCAAAGTCTGATGTTTACTGTG T C PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:71820202..71820380 26863196 MeRIP-seq:(Medium) rs113554687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_381661,Human_RBP_ID_861229,Human_RBP_ID_22752590,Human_RBP_ID_23467165,Human_RBP_ID_24829623 Human_Splice_Rec_1144474,Human_Splice_Rec_1144475,Human_Splice_Rec_1144512,Human_Splice_Rec_1144513,Human_Splice_Rec_1144526,Human_Splice_Rec_1144527,Human_Splice_Rec_1144536,Human_Splice_Rec_1144537 Human_miRNA_ID_2745262,Human_miRNA_ID_2745263 RMVar_hsa_circ_124965,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_91301,RMVar_hsa_circ_100972,RMVar_hsa_circ_144117,RMVar_hsa_circ_144121,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144119,RMVar_hsa_circ_144120,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114,RMVar_hsa_circ_56643,RMVar_hsa_circ_106163,RMVar_hsa_circ_113779,RMVar_hsa_circ_144126,RMVar_hsa_circ_118638,RMVar_hsa_circ_144125,RMVar_hsa_circ_109871,RMVar_hsa_circ_144129,RMVar_hsa_circ_94744,RMVar_hsa_circ_144131,RMVar_hsa_circ_91252,RMVar_hsa_circ_144130,RMVar_hsa_circ_144127,RMVar_hsa_circ_144128,RMVar_hsa_circ_373264,RMVar_hsa_circ_84326,RMVar_hsa_circ_77099,RMVar_hsa_circ_144134,RMVar_hsa_circ_340945,RMVar_hsa_circ_144135,RMVar_hsa_circ_144136,RMVar_hsa_circ_107317,RMVar_hsa_circ_144138,RMVar_hsa_circ_43856,RMVar_hsa_circ_63375,RMVar_hsa_circ_144139,RMVar_hsa_circ_144141,RMVar_hsa_circ_144140 78674 RMVar_ID_78674 Human_SNP_ID_437310175 m1A Human chr10 + 71828066 71828066 71828066 CCAGGCGGTCACACTCCTCCTTGACATGTTCCACCAAGGCCTGGACAAAGGTGGAGTTGGTCCGT CCAGGCGGTCACACTCCTCCTTGACATGTTCCCCCAAGGCCTGGACAAAGGTGGAGTTGGTCCGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:71827950..71828110 26863196 MeRIP-seq:(Medium) rs758534857 Functional Loss SNV dbSNP153 33..33 33 - - - 78675 RMVar_ID_78675 Human_SNP_ID_437310176 m1A Human chr10 + 71828066 71828066 71828066 CCAGGCGGTCACACTCCTCCTTGACATGTTCCACCAAGGCCTGGACAAAGGTGGAGTTGGTCCGT CCAGGCGGTCACACTCCTCCTTGACATGTTCCTCCAAGGCCTGGACAAAGGTGGAGTTGGTCCGT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:71827950..71828110 26863196 MeRIP-seq:(Medium) rs758534857 Functional Loss SNV dbSNP153 33..33 33 - - - 78676 RMVar_ID_78676 Human_SNP_ID_437310208 m1A Human chr10 - 71828156 71828156 71828156 TAAGTTGCAAACCTAACTGCCTCTTCTGTAGGATAATGGGGACGTTTGCCAGGACTGCATTCAGA TAAGTTGCAAACCTAACTGCCTCTTCTGTAGGGTAATGGGGACGTTTGCCAGGACTGCATTCAGA T C PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:71828151..71828175 26863196 MeRIP-seq:(Medium) rs138636858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26881621 Human_Splice_Rec_1144468,Human_Splice_Rec_1144508 RMVar_hsa_circ_124965,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_144117,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144119,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114,RMVar_hsa_circ_56643,RMVar_hsa_circ_113779,RMVar_hsa_circ_144126,RMVar_hsa_circ_144129,RMVar_hsa_circ_94744,RMVar_hsa_circ_91252,RMVar_hsa_circ_144127,RMVar_hsa_circ_144128,RMVar_hsa_circ_63375,RMVar_hsa_circ_121819,RMVar_hsa_circ_92109,RMVar_hsa_circ_144147,RMVar_hsa_circ_106430,RMVar_hsa_circ_144142,RMVar_hsa_circ_144143,RMVar_hsa_circ_107333,RMVar_hsa_circ_374222,RMVar_hsa_circ_97105,RMVar_hsa_circ_101664,RMVar_hsa_circ_144149,RMVar_hsa_circ_144151,RMVar_hsa_circ_94533,RMVar_hsa_circ_144150,RMVar_hsa_circ_144148,RMVar_hsa_circ_91440,RMVar_hsa_circ_116506,RMVar_hsa_circ_144146,RMVar_hsa_circ_376093,RMVar_hsa_circ_109048,RMVar_hsa_circ_144153,RMVar_hsa_circ_144154,RMVar_hsa_circ_144155,RMVar_hsa_circ_144152 78677 RMVar_ID_78677 Human_SNP_ID_437311092 m1A Human chr10 - 71831229 71831229 71831229 CCTCTCGTAGGAGGAGATCCTTGTTTACTTGGAGAAGACCTGTGACTGGCTTCCGAAACCGAACA CCTCTCGTAGGAGGAGATCCTTGTTTACTTGGTGAAGACCTGTGACTGGCTTCCGAAACCGAACA T A PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:71831178..71831282 26863196 MeRIP-seq:(Medium) rs778854258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_381678,Human_RBP_ID_1449435,Human_RBP_ID_1770055,Human_RBP_ID_8991795,Human_RBP_ID_11413921,Human_RBP_ID_18416437,Human_RBP_ID_18597385,Human_RBP_ID_22432463,Human_RBP_ID_22639418,Human_RBP_ID_22752440,Human_RBP_ID_23467208 Human_Splice_Rec_1144464,Human_Splice_Rec_1144490,Human_Splice_Rec_1144504 Human_miRNA_ID_2777529,Human_miRNA_ID_2789259,Human_miRNA_ID_2818871,Human_miRNA_ID_3003998 RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_144117,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114,RMVar_hsa_circ_56643,RMVar_hsa_circ_94744,RMVar_hsa_circ_91252,RMVar_hsa_circ_144127,RMVar_hsa_circ_144128,RMVar_hsa_circ_63375,RMVar_hsa_circ_121819,RMVar_hsa_circ_92109,RMVar_hsa_circ_144142,RMVar_hsa_circ_144143,RMVar_hsa_circ_107333,RMVar_hsa_circ_97105,RMVar_hsa_circ_101664,RMVar_hsa_circ_144149,RMVar_hsa_circ_144151,RMVar_hsa_circ_94533,RMVar_hsa_circ_144150,RMVar_hsa_circ_144148,RMVar_hsa_circ_116506,RMVar_hsa_circ_376093,RMVar_hsa_circ_109048,RMVar_hsa_circ_347664,RMVar_hsa_circ_144153,RMVar_hsa_circ_144154,RMVar_hsa_circ_144155,RMVar_hsa_circ_61664,RMVar_hsa_circ_339145,RMVar_hsa_circ_357173,RMVar_hsa_circ_144156 78678 RMVar_ID_78678 Human_SNP_ID_437311093 m1A Human chr10 - 71831229 71831229 71831229 CCTCTCGTAGGAGGAGATCCTTGTTTACTTGGAGAAGACCTGTGACTGGCTTCCGAAACCGAACA CCTCTCGTAGGAGGAGATCCTTGTTTACTTGGGGAAGACCTGTGACTGGCTTCCGAAACCGAACA T C PSAP Ensembl:ENSG00000197746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:71831178..71831282 26863196 MeRIP-seq:(Medium) rs778854258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_381678,Human_RBP_ID_1449435,Human_RBP_ID_1770055,Human_RBP_ID_8991795,Human_RBP_ID_11413921,Human_RBP_ID_18416437,Human_RBP_ID_18597385,Human_RBP_ID_22432463,Human_RBP_ID_22639418,Human_RBP_ID_22752440,Human_RBP_ID_23467208 Human_Splice_Rec_1144464,Human_Splice_Rec_1144490,Human_Splice_Rec_1144504 Human_miRNA_ID_2777529,Human_miRNA_ID_2789259,Human_miRNA_ID_2818871,Human_miRNA_ID_3003998 RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_144117,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114,RMVar_hsa_circ_56643,RMVar_hsa_circ_94744,RMVar_hsa_circ_91252,RMVar_hsa_circ_144127,RMVar_hsa_circ_144128,RMVar_hsa_circ_63375,RMVar_hsa_circ_121819,RMVar_hsa_circ_92109,RMVar_hsa_circ_144142,RMVar_hsa_circ_144143,RMVar_hsa_circ_107333,RMVar_hsa_circ_97105,RMVar_hsa_circ_101664,RMVar_hsa_circ_144149,RMVar_hsa_circ_144151,RMVar_hsa_circ_94533,RMVar_hsa_circ_144150,RMVar_hsa_circ_144148,RMVar_hsa_circ_116506,RMVar_hsa_circ_376093,RMVar_hsa_circ_109048,RMVar_hsa_circ_347664,RMVar_hsa_circ_144153,RMVar_hsa_circ_144154,RMVar_hsa_circ_144155,RMVar_hsa_circ_61664,RMVar_hsa_circ_339145,RMVar_hsa_circ_357173,RMVar_hsa_circ_144156 78679 RMVar_ID_78679 Human_SNP_ID_437316468 m1A Human chr10 - 71851231 71851231 71851231 AGCTGACGCTCCGCATTGCAGACTGCGGAGTCAGACGGCGCTATGTACGCCCTCTTCCTCCTGGC AGCTGACGCTCCGCATTGCAGACTGCGGAGTCGGACGGCGCTATGTACGCCCTCTTCCTCCTGGC T C PSAP Ensembl:ENSG00000197746 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:71851133..71851300 26863196 MeRIP-seq:(Medium) rs76455588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28263,Human_RBP_ID_4126194,Human_RBP_ID_9320598,Human_RBP_ID_11414325,Human_RBP_ID_26881630 Human_Splice_Rec_1144459,Human_Splice_Rec_1144485,Human_Splice_Rec_1144499 Human_miRNA_ID_2453963 Clinvar_Rec_363 RMVar_hsa_circ_116761,RMVar_hsa_circ_144114,RMVar_hsa_circ_94744,RMVar_hsa_circ_144127,RMVar_hsa_circ_101664,RMVar_hsa_circ_144151,RMVar_hsa_circ_109048,RMVar_hsa_circ_144155 78680 RMVar_ID_78680 Human_SNP_ID_437316483 m1A Human chr10 - 71851244 71851244 71851244 TCTGCGGGGGATCAGCTGACGCTCCGCATTGCAGACTGCGGAGTCAGACGGCGCTATGTACGCCC TCTGCGGGGGATCAGCTGACGCTCCGCATTGCGGACTGCGGAGTCAGACGGCGCTATGTACGCCC T C PSAP Ensembl:ENSG00000197746 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1191567165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4126194,Human_RBP_ID_5459438,Human_RBP_ID_11414325,Human_RBP_ID_24829685 Human_Splice_Rec_1144459,Human_Splice_Rec_1144485,Human_Splice_Rec_1144499 Human_miRNA_ID_2453963 RMVar_hsa_circ_116761,RMVar_hsa_circ_144114,RMVar_hsa_circ_94744,RMVar_hsa_circ_144127,RMVar_hsa_circ_101664,RMVar_hsa_circ_144151,RMVar_hsa_circ_109048,RMVar_hsa_circ_144155 78681 RMVar_ID_78681 Human_SNP_ID_437327508 m1A Human chr10 - 71889176 71889176 71889176 GGGACCCACTCGACGCTGCCCGCGCATGCCCCAACCCGTTCGTGCCCCCGCCTGGCCGCGTGCAG GGGACCCACTCGACGCTGCCCGCGCATGCCCCCACCCGTTCGTGCCCCCGCCTGGCCGCGTGCAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:71889056..71889198 26863196 MeRIP-seq:(Medium) rs1489718933 Functional Loss SNV dbSNP153 33..33 33 - - - 78682 RMVar_ID_78682 Human_SNP_ID_437356915 m1A Human chr10 - 72008053 72008053 72008053 CGGACAGGCGGATGCTCTCGCAGTTGCCCCGCAGCCGCTGCACCTCCTCTTCCCTCAGGCCGTCC CGGACAGGCGGATGCTCTCGCAGTTGCCCCGCTGCCGCTGCACCTCCTCTTCCCTCAGGCCGTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:72008005..72008217 26863196 MeRIP-seq:(Medium) rs755903839 Functional Loss SNV dbSNP153 33..33 33 - - - 78683 RMVar_ID_78683 Human_SNP_ID_437370922 m1A Human chr10 - 72062826 72062826 72062826 GAGGATGAGGAGGAGAAGGAGACGGAGGAAGCAGGCGAGGAGGCCGAGGAGGAGGAGGGCGAGGC GAGGATGAGGAGGAGAAGGAGACGGAGGAAGCCGGCGAGGAGGCCGAGGAGGAGGAGGGCGAGGC T G SPOCK2 Ensembl:ENSG00000107742 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72062775..72062864 26863196 MeRIP-seq:(Medium) rs753248395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17229939,Human_RBP_ID_22752849 Human_Splice_Rec_1144564,Human_Splice_Rec_1144586,Human_Splice_Rec_1144602,Human_Splice_Rec_1144614,Human_Splice_Rec_1144626 78684 RMVar_ID_78684 Human_SNP_ID_437424712 m1A Human chr10 - 72273979 72273979 72273979 TGAATGGGTGTGCGAACCCGTGCCAACCACCGAGAGCCGCCCAGACCCGTCCCAGGTCCACGCTC TGAATGGGTGTGCGAACCCGTGCCAACCACCGTGAGCCGCCCAGACCCGTCCCAGGTCCACGCTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:72273926..72274550;chr10:72273926..72274625 26863196 MeRIP-seq:(Medium) rs958846581 Functional Loss SNV dbSNP153 33..33 33 - - - 78685 RMVar_ID_78685 Human_SNP_ID_437425147 m1A Human chr10 - 72274998 72274998 72274998 GGCGCAGCACGAGGGTCAGCTGGAAGGTGGGCACCAGGCTGGGGTCGAGTGCCAGCTGGCCCACG GGCGCAGCACGAGGGTCAGCTGGAAGGTGGGCGCCAGGCTGGGGTCGAGTGCCAGCTGGCCCACG T C DDIT4-AS1 Ensembl:ENSG00000269926 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:72274676..72275150 32194978 MeRIP-seq:(Medium) rs904854970 Functional Loss SNV dbSNP153 33..33 33 - - - 78686 RMVar_ID_78686 Human_SNP_ID_437425154 m1A Human chr10 - 72275019 72275019 72275019 TGGGCCAGAGTCGTGAGTCCAGGCGCAGCACGAGGGTCAGCTGGAAGGTGGGCACCAGGCTGGGG TGGGCCAGAGTCGTGAGTCCAGGCGCAGCACGCGGGTCAGCTGGAAGGTGGGCACCAGGCTGGGG T G DDIT4-AS1 Ensembl:ENSG00000269926 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72274697..72275345 26863196 MeRIP-seq:(Medium) rs1410025506 Functional Loss SNV dbSNP153 33..33 33 - - - 78687 RMVar_ID_78687 Human_SNP_ID_437431290 m1A Human chr10 + 72297882 72297882 72297882 TCCGCCTCCTGCACGGCCTCCGCCTCCGCCTGACCGTCCTCGGAAACCTCCCAGCCGCAGCCCGG TCCGCCTCCTGCACGGCCTCCGCCTCCGCCTGTCCGTCCTCGGAAACCTCCCAGCCGCAGCCCGG A T HSALNG0078775 RNACentral:URS0000EB43F2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72297831..72297983 26863196 MeRIP-seq:(Medium) rs948859503 Functional Loss SNV dbSNP153 33..33 33 - - - 78688 RMVar_ID_78688 Human_SNP_ID_437445987 m1A Human chr10 - 72352280 72352280 72352280 TGGAGGTGGTAATTCGTATACAGAGAGGATTAAGTTTGGGAAATAAAATGGGGCCAGATCATAGA TGGAGGTGGTAATTCGTATACAGAGAGGATTAGGTTTGGGAAATAAAATGGGGCCAGATCATAGA T C DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72352278..72352468 26863196 MeRIP-seq:(Medium) rs113559374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5996256,Human_RBP_ID_11417833,Human_RBP_ID_23467660 RMVar_hsa_circ_76719,RMVar_hsa_circ_144187 78689 RMVar_ID_78689 Human_SNP_ID_437445988 m1A Human chr10 - 72352280 72352280 72352280 TGGAGGTGGTAATTCGTATACAGAGAGGATTAAGTTTGGGAAATAAAATGGGGCCAGATCATAGA TGGAGGTGGTAATTCGTATACAGAGAGGATTACGTTTGGGAAATAAAATGGGGCCAGATCATAGA T G DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72352278..72352468 26863196 MeRIP-seq:(Medium) rs113559374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5996256,Human_RBP_ID_11417833,Human_RBP_ID_23467660 RMVar_hsa_circ_76719,RMVar_hsa_circ_144187 78690 RMVar_ID_78690 Human_SNP_ID_437446638 m1A Human chr10 - 72354839 72354839 72354839 GCGCTGTATCAGCATCGCCCTCAAGGCCATCCAGAGCAACCAGCCCGACCGGGCGCTCCGCTTCC GCGCTGTATCAGCATCGCCCTCAAGGCCATCCGGAGCAACCAGCCCGACCGGGCGCTCCGCTTCC T C DNAJB12 Ensembl:ENSG00000148719 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:72354743..72354934 26863196 MeRIP-seq:(Medium) rs758836464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136349 Human_Splice_Rec_1144985,Human_Splice_Rec_1145001,Human_Splice_Rec_1145015 RMVar_hsa_circ_76719,RMVar_hsa_circ_144187 78691 RMVar_ID_78691 Human_SNP_ID_437488343 m1A Human chr10 - 72533021 72533019 72533022 GTTCTACAAAGCACAATGAACAGGAAGTCAGAAGGACAATCATGGAGTGGCTGGAAAAGGCAGGA GTTCTACAAAGCACAATGAACAGGAAGTCAG___GACAATCATGGAGTGGCTGGAAAAGGCAGGA CCTT C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72533015..72533092 26863196 MeRIP-seq:(Medium) rs758955750 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11418393 RMVar_hsa_circ_64120,RMVar_hsa_circ_343727,RMVar_hsa_circ_347521,RMVar_hsa_circ_341762,RMVar_hsa_circ_87344,RMVar_hsa_circ_284137,RMVar_hsa_circ_144192,RMVar_hsa_circ_144193 78692 RMVar_ID_78692 Human_SNP_ID_437488344 m1A Human chr10 - 72533021 72533021 72533021 GTTCTACAAAGCACAATGAACAGGAAGTCAGAAGGACAATCATGGAGTGGCTGGAAAAGGCAGGA GTTCTACAAAGCACAATGAACAGGAAGTCAGACGGACAATCATGGAGTGGCTGGAAAAGGCAGGA T G MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:72533015..72533092 26863196 MeRIP-seq:(Medium) rs1273489009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11418393 RMVar_hsa_circ_64120,RMVar_hsa_circ_343727,RMVar_hsa_circ_347521,RMVar_hsa_circ_341762,RMVar_hsa_circ_87344,RMVar_hsa_circ_284137,RMVar_hsa_circ_144192,RMVar_hsa_circ_144193 78693 RMVar_ID_78693 Human_SNP_ID_437510227 m1A Human chr10 - 72625957 72625946 72625958 GGTATAAGGAGACAGCAATTTAGGGAAGGCGAAGGGGAAGGGGGTTGGCGAGACAGCCTTAGGGA GGTATAAGGAGACAGCAATTTAGGGAAGGCG____________GTTGGCGAGACAGCCTTAGGGA CCCCCTTCCCCTT C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:72625953..72626046 26863196 MeRIP-seq:(Medium) rs201357033 Functional Loss DEL dbSNP153 32..43 33 - - - 78694 RMVar_ID_78694 Human_SNP_ID_437526441 m1A Human chr10 - 72692248 72692248 72692248 CCGGTGGCGGCTGACGCCCAGCCCAGGGAAGCAGCCGGCAGTCAGCGCCCCGCAGCCGCCGGCGC CCGGTGGCGGCTGACGCCCAGCCCAGGGAAGCGGCCGGCAGTCAGCGCCCCGCAGCCGCCGGCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:72692151..72692300 26863410 MeRIP-seq:(Medium) rs1320407832 Functional Loss SNV dbSNP153 33..33 33 - - - 78695 RMVar_ID_78695 Human_SNP_ID_437526442 m1A Human chr10 - 72692248 72692248 72692248 CCGGTGGCGGCTGACGCCCAGCCCAGGGAAGCAGCCGGCAGTCAGCGCCCCGCAGCCGCCGGCGC CCGGTGGCGGCTGACGCCCAGCCCAGGGAAGCCGCCGGCAGTCAGCGCCCCGCAGCCGCCGGCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:72692151..72692300 26863410 MeRIP-seq:(Medium) rs1320407832 Functional Loss SNV dbSNP153 33..33 33 - - - 78696 RMVar_ID_78696 Human_SNP_ID_437526678 m1A Human chr10 + 72692997 72692997 72692997 TAAAGGTGCTTTTGGGGGTCCTTTCGAGGGCTACTGTATAAGCGTGTTCACGCGTGCCTGAAGCG TAAAGGTGCTTTTGGGGGTCCTTTCGAGGGCTGCTGTATAAGCGTGTTCACGCGTGCCTGAAGCG A G MCU Ensembl:ENSG00000156026 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:72692959..72693077 26863196 MeRIP-seq:(Medium) rs531885120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2229791,Human_RBP_ID_5313257,Human_RBP_ID_23467896 Human_Splice_Rec_1145289,Human_Splice_Rec_1145303 RMVar_hsa_circ_91938,RMVar_hsa_circ_144200 78697 RMVar_ID_78697 Human_SNP_ID_437565124 m1A Human chr10 - 72859189 72859189 72859189 TCACAGATATCACAGGTAACCCATTTTGATAAACCACTGTAACATCTGAATGAAAAAGACCCACA TCACAGATATCACAGGTAACCCATTTTGATAAGCCACTGTAACATCTGAATGAAAAAGACCCACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:72859184..72859285 32194978 MeRIP-seq:(Medium) rs1488982583 Functional Loss SNV dbSNP153 33..33 33 - - - 78698 RMVar_ID_78698 Human_SNP_ID_437578778 m1A Human chr10 - 72917834 72917834 72917834 ACACCAAGATCAAAAGGACAAGAATCCTTCAAAAAACAGGAAAAAACTCCTAAAACACCAAAAGG ACACCAAGATCAAAAGGACAAGAATCCTTCAAGAAACAGGAAAAAACTCCTAAAACACCAAAAGG T C NPM1P24 Ensembl:ENSG00000215086 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879075827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6024780 78699 RMVar_ID_78699 Human_SNP_ID_437609866 m1A Human chr10 + 73047045 73047045 73047045 TCCTCCTGTTTAGCTGGAGCCAGAATAAATTTAGGATTACGGTTTCCATCATGGTAGCGGCAAAA TCCTCCTGTTTAGCTGGAGCCAGAATAAATTTGGGATTACGGTTTCCATCATGGTAGCGGCAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73046994..73051245 32194978 MeRIP-seq:(Medium) rs201803227 Functional Loss SNV dbSNP153 33..33 33 - - - 78700 RMVar_ID_78700 Human_SNP_ID_437611463 m1A Human chr10 + 73053587 73053587 73053587 AGTCCTCAGCCGTTAGAAAAGATTTGTGTTTCACTCCTATGAAAAGAAAATACAGAGAACTTTAG AGTCCTCAGCCGTTAGAAAAGATTTGTGTTTCGCTCCTATGAAAAGAAAATACAGAGAACTTTAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73053545..73068901 32194978 MeRIP-seq:(Medium) rs775762415 Functional Loss SNV dbSNP153 33..33 33 - - - 78701 RMVar_ID_78701 Human_SNP_ID_437622246 m1A Human chr10 - 73096634 73096634 73096634 TCTGGGGCGGGGGTTCCCCAGGTTACCACAGCAGCCTCGGTTCCTTCCCCTCGGGAGACTCGGCC TCTGGGGCGGGGGTTCCCCAGGTTACCACAGCGGCCTCGGTTCCTTCCCCTCGGGAGACTCGGCC T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:73096594..73096728 26863196 MeRIP-seq:(Medium) rs1398491114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 78702 RMVar_ID_78702 Human_SNP_ID_437622247 m1A Human chr10 - 73096637 73096637 73096637 ACTTCTGGGGCGGGGGTTCCCCAGGTTACCACAGCAGCCTCGGTTCCTTCCCCTCGGGAGACTCG ACTTCTGGGGCGGGGGTTCCCCAGGTTACCACCGCAGCCTCGGTTCCTTCCCCTCGGGAGACTCG T G P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:73096634..73096754 32194978 MeRIP-seq:(Medium) rs1188354634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5997767 RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 78703 RMVar_ID_78703 Human_SNP_ID_437622295 m1A Human chr10 + 73096781 73096781 73096781 TCGAGGGAGCGTCTCACCTGGAAAGTGGGACGAGAGGGCGGCGCGCTCTTCAGCCCCCAGTCGCC TCGAGGGAGCGTCTCACCTGGAAAGTGGGACGTGAGGGCGGCGCGCTCTTCAGCCCCCAGTCGCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73074824..73096874 32194978 MeRIP-seq:(Medium) rs201134651 Functional Loss SNV dbSNP153 33..33 33 - - - 78704 RMVar_ID_78704 Human_SNP_ID_437635262 m1A Human chr10 + 73152398 73152398 73152398 TCTGGCACAAACCTTTGTTGCACCAATTGTGCATATAGACATTTAGTGAATGTGACCTGGGCATC TCTGGCACAAACCTTTGTTGCACCAATTGTGCCTATAGACATTTAGTGAATGTGACCTGGGCATC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73148394..73156291 32194978 MeRIP-seq:(Medium) rs201647688 Functional Loss SNV dbSNP153 33..33 33 - - - 78705 RMVar_ID_78705 Human_SNP_ID_437635263 m1A Human chr10 + 73152398 73152398 73152398 TCTGGCACAAACCTTTGTTGCACCAATTGTGCATATAGACATTTAGTGAATGTGACCTGGGCATC TCTGGCACAAACCTTTGTTGCACCAATTGTGCGTATAGACATTTAGTGAATGTGACCTGGGCATC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73148394..73156291 32194978 MeRIP-seq:(Medium) rs201647688 Functional Loss SNV dbSNP153 33..33 33 - - - 78706 RMVar_ID_78706 Human_SNP_ID_437638087 m1A Human chr10 - 73163862 73163862 73163862 AGTACTGCCTGTTCCTGATACCAGATGAGTCAAGGGACTCAGATAAACATAAAGAGATTCTTCAG AGTACTGCCTGTTCCTGATACCAGATGAGTCAGGGGACTCAGATAAACATAAAGAGATTCTTCAG T C ECD Ensembl:ENSG00000122882 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73163760..73163861 32194978 MeRIP-seq:(Medium) rs774499265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_192355,Human_RBP_ID_862436,Human_RBP_ID_9360456,Human_RBP_ID_18597766,Human_RBP_ID_18970029,Human_RBP_ID_26881895 Human_Splice_Rec_1145632,Human_Splice_Rec_1145680,Human_Splice_Rec_1145704,Human_Splice_Rec_1145742,Human_Splice_Rec_1145752 Human_miRNA_ID_891022,Human_miRNA_ID_2210387,Human_miRNA_ID_2403868 RMVar_hsa_circ_32760,RMVar_hsa_circ_2347,RMVar_hsa_circ_144247,RMVar_hsa_circ_12245,RMVar_hsa_circ_311340,RMVar_hsa_circ_144251,RMVar_hsa_circ_299308,RMVar_hsa_circ_144254,RMVar_hsa_circ_292546,RMVar_hsa_circ_144258,RMVar_hsa_circ_19895,RMVar_hsa_circ_307507,RMVar_hsa_circ_325053 78707 RMVar_ID_78707 Human_SNP_ID_437639025 m1A Human chr10 - 73167947 73167947 73167947 AGAGCCTGATCCAGGCTTCGGCGGCCGGTGGCAGCTCTCGATCAGCTCTCGCAGTCGGAGAGGCG AGAGCCTGATCCAGGCTTCGGCGGCCGGTGGCGGCTCTCGATCAGCTCTCGCAGTCGGAGAGGCG T C ECD Ensembl:ENSG00000122882 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr10:73167898..73168006;chr10:73167897..73167997 26863196 MeRIP-seq:(Medium) rs1423756403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136354,Human_RBP_ID_8762974 Human_Splice_Rec_1145631,Human_Splice_Rec_1145657,Human_Splice_Rec_1145679,Human_Splice_Rec_1145703,Human_Splice_Rec_1145731,Human_Splice_Rec_1145741 78708 RMVar_ID_78708 Human_SNP_ID_437641410 m1A Human chr10 + 73177797 73177797 73177797 CTGAGTAGTTAATGCCACAGAAACTTGAGGACATATGAAAAATTTTCTTTTTTCTCTCCTCCTCC CTGAGTAGTTAATGCCACAGAAACTTGAGGACCTATGAAAAATTTTCTTTTTTCTCTCCTCCTCC A C FAM149B1 Ensembl:ENSG00000138286 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73177789..73177888 26863196 MeRIP-seq:(Medium) rs1038080050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3953,RMVar_hsa_circ_290111,RMVar_hsa_circ_304562,RMVar_hsa_circ_323868,RMVar_hsa_circ_279343,RMVar_hsa_circ_288097,RMVar_hsa_circ_51977,RMVar_hsa_circ_144261,RMVar_hsa_circ_144263,RMVar_hsa_circ_144264,RMVar_hsa_circ_144265,RMVar_hsa_circ_144262,RMVar_hsa_circ_144260 78709 RMVar_ID_78709 Human_SNP_ID_437641411 m1A Human chr10 + 73177797 73177797 73177797 CTGAGTAGTTAATGCCACAGAAACTTGAGGACATATGAAAAATTTTCTTTTTTCTCTCCTCCTCC CTGAGTAGTTAATGCCACAGAAACTTGAGGACGTATGAAAAATTTTCTTTTTTCTCTCCTCCTCC A G FAM149B1 Ensembl:ENSG00000138286 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73177789..73177888 26863196 MeRIP-seq:(Medium) rs1038080050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3953,RMVar_hsa_circ_290111,RMVar_hsa_circ_304562,RMVar_hsa_circ_323868,RMVar_hsa_circ_279343,RMVar_hsa_circ_288097,RMVar_hsa_circ_51977,RMVar_hsa_circ_144261,RMVar_hsa_circ_144263,RMVar_hsa_circ_144264,RMVar_hsa_circ_144265,RMVar_hsa_circ_144262,RMVar_hsa_circ_144260 78710 RMVar_ID_78710 Human_SNP_ID_437653723 m1A Human chr10 - 73234842 73234842 73234842 ATTATTTCGACTCAGGGGCGTCGGTGAGGGAGAGGAGAGCGAGTCGGGTGCCACTGGGCTGCAGA ATTATTTCGACTCAGGGGCGTCGGTGAGGGAGGGGAGAGCGAGTCGGGTGCCACTGGGCTGCAGA T C DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73234797..73234893 26863196 MeRIP-seq:(Medium) rs1269784286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1261940,Human_RBP_ID_5998164 78711 RMVar_ID_78711 Human_SNP_ID_437655967 m1A Human chr10 - 73243486 73243486 73243486 GCAGACAAAAGGATCGGCAAAAGGAAATGGACAATTTTCTGGCTCAGATGGAAGCAAAGTACTGC GCAGACAAAAGGATCGGCAAAAGGAAATGGACGATTTTCTGGCTCAGATGGAAGCAAAGTACTGC T C DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73243451..73243525 32194978 MeRIP-seq:(Medium) rs1249117781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1449766,Human_RBP_ID_1770392,Human_RBP_ID_5998277,Human_RBP_ID_11422710,Human_RBP_ID_17648050,Human_RBP_ID_18525689,Human_RBP_ID_22490278 Human_Splice_Rec_1145854 RMVar_hsa_circ_144273,RMVar_hsa_circ_76722 78712 RMVar_ID_78712 Human_SNP_ID_437656904 m1A Human chr10 - 73246795 73246795 73246795 TCCTGGGAAAAGTCTATTCCGTTCTCAGTGACAGAGAACAGAGAGCAGTGTACGATGAGCAGGGA TCCTGGGAAAAGTCTATTCCGTTCTCAGTGACGGAGAACAGAGAGCAGTGTACGATGAGCAGGGA T C DNAJC9 Ensembl:ENSG00000213551 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73246744..73246875 26863196 MeRIP-seq:(Medium) rs1365201368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382089,Human_RBP_ID_1449774,Human_RBP_ID_4136356,Human_RBP_ID_5137883,Human_RBP_ID_9360459,Human_RBP_ID_11422782,Human_RBP_ID_17782258,Human_RBP_ID_18597813,Human_RBP_ID_22788667,Human_RBP_ID_24853372,Human_RBP_ID_26316411,Human_RBP_ID_26881932 Human_Splice_Rec_1145848 RMVar_hsa_circ_144274,RMVar_hsa_circ_312230,RMVar_hsa_circ_268807 78713 RMVar_ID_78713 Human_SNP_ID_437657095 m1A Human chr10 + 73247134 73247134 73247134 CGCCGTCGGAGGCCTCGCGTCGCACGCCCAGCACCCGGTAAAGGTCGGCGGTGCCGAACACTTCC CGCCGTCGGAGGCCTCGCGTCGCACGCCCAGCGCCCGGTAAAGGTCGGCGGTGCCGAACACTTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73247084..73247189 26863196 MeRIP-seq:(Medium) rs1357071933 Functional Loss SNV dbSNP153 33..33 33 - - - 78714 RMVar_ID_78714 Human_SNP_ID_437657120 m1A Human chr10 - 73247189 73247189 73247189 CTGCTTCCTCCGGGGTCGTATCTCCGCCCGGCATGGGGCTGCTGGACCTTTGCGAGGAAGTGTTC CTGCTTCCTCCGGGGTCGTATCTCCGCCCGGCTTGGGGCTGCTGGACCTTTGCGAGGAAGTGTTC T A DNAJC9 Ensembl:ENSG00000213551 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:73247143..73247225 26863196 MeRIP-seq:(Medium) rs1338333825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382094,Human_RBP_ID_1449781,Human_RBP_ID_4135889,Human_RBP_ID_5273659,Human_RBP_ID_5998297,Human_RBP_ID_8762986,Human_RBP_ID_8940378,Human_RBP_ID_9320604,Human_RBP_ID_11422788,Human_RBP_ID_18416274,Human_RBP_ID_18597818,Human_RBP_ID_18970031 78715 RMVar_ID_78715 Human_SNP_ID_437657121 m1A Human chr10 - 73247189 73247189 73247189 CTGCTTCCTCCGGGGTCGTATCTCCGCCCGGCATGGGGCTGCTGGACCTTTGCGAGGAAGTGTTC CTGCTTCCTCCGGGGTCGTATCTCCGCCCGGCGTGGGGCTGCTGGACCTTTGCGAGGAAGTGTTC T C DNAJC9 Ensembl:ENSG00000213551 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:73247143..73247225 26863196 MeRIP-seq:(Medium) rs1338333825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382094,Human_RBP_ID_1449781,Human_RBP_ID_4135889,Human_RBP_ID_5273659,Human_RBP_ID_5998297,Human_RBP_ID_8762986,Human_RBP_ID_8940378,Human_RBP_ID_9320604,Human_RBP_ID_11422788,Human_RBP_ID_18416274,Human_RBP_ID_18597818,Human_RBP_ID_18970031 78716 RMVar_ID_78716 Human_SNP_ID_437657152 m1A Human chr10 + 73247220 73247220 73247220 ATGCCGGGCGGAGATACGACCCCGGAGGAAGCAGCCGCTCCCAGCTGCGCCGGGTACAACCCAGG ATGCCGGGCGGAGATACGACCCCGGAGGAAGCTGCCGCTCCCAGCTGCGCCGGGTACAACCCAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73246988..73247275 26863196 MeRIP-seq:(Medium) rs1328005871 Functional Loss SNV dbSNP153 33..33 33 - - - 78717 RMVar_ID_78717 Human_SNP_ID_437657736 m1A Human chr10 - 73249030 73249030 73249030 CCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAGATCACTTGAGCCCAGGAGGCCGATGCT CCCATAGTTCCAGCTACTCGGGAAGCTGAGGCGGTAAGATCACTTGAGCCCAGGAGGCCGATGCT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73248979..73249276 32194978 MeRIP-seq:(Medium) rs1344699024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382133,Human_RBP_ID_11422908,Human_RBP_ID_17782268,Human_RBP_ID_26396659 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 78718 RMVar_ID_78718 Human_SNP_ID_437657737 m1A Human chr10 - 73249034 73249034 73249034 CTCACCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAGATCACTTGAGCCCAGGAGGCCGA CTCACCCATAGTTCCAGCTACTCGGGAAGCTGGGGCAGTAAGATCACTTGAGCCCAGGAGGCCGA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1133548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382133,Human_RBP_ID_11422908,Human_RBP_ID_17782268,Human_RBP_ID_26396659 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 78719 RMVar_ID_78719 Human_SNP_ID_437657751 m1A Human chr10 - 73249097 73249097 73249097 CTGTGCAACACAGCAAGACCCCGTCTCTACAAAAACTTAAAAAATTAGCTGGCTGTGGTGTTGCT CTGTGCAACACAGCAAGACCCCGTCTCTACAAGAACTTAAAAAATTAGCTGGCTGTGGTGTTGCT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1133537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9606916,Human_RBP_ID_17782270,Human_RBP_ID_22887772,Human_RBP_ID_24860697,Human_RBP_ID_27408313 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 78720 RMVar_ID_78720 Human_SNP_ID_437657774 m1A Human chr10 - 73249197 73249197 73249197 AATATAAAGATACCATTGGGGCAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGT AATATAAAGATACCATTGGGGCAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1054858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172668,Human_RBP_ID_23152758,Human_RBP_ID_26398409 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 78721 RMVar_ID_78721 Human_SNP_ID_437658079 m1A Human chr10 - 73250329 73250329 73250329 CAGGCTGGAGTGCGGTGGTGCAATCTCAGCTCACTGCAATCTCCACCTCCTGGGTTCAAGAGGTT CAGGCTGGAGTGCGGTGGTGCAATCTCAGCTCGCTGCAATCTCCACCTCCTGGGTTCAAGAGGTT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1342595528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382147,Human_RBP_ID_8172674,Human_RBP_ID_9623602,Human_RBP_ID_22884436,Human_RBP_ID_24831909,Human_RBP_ID_26396698 Human_miRNA_ID_866461,Human_miRNA_ID_1984725,Human_miRNA_ID_2940359 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 78722 RMVar_ID_78722 Human_SNP_ID_437658686 m1A Human chr10 + 73252017 73252015 73252017 TTAAGTGGCCCCCACGGTAGGCCTTGCAGAGGAGAGTAGCTGTAGAAAAGCAGCTGGTTAGGACA TTAAGTGGCCCCCACGGTAGGCCTTGCAGAG__GAGTAGCTGTAGAAAAGCAGCTGGTTAGGACA GGA G DNAJC9-AS1 Ensembl:ENSG00000236756 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:73251800..73252064 26863196 MeRIP-seq:(Medium) rs775532035 Functional Loss DEL dbSNP153 32..33 33 - - - 78723 RMVar_ID_78723 Human_SNP_ID_437658825 m1A Human chr10 - 73252398 73252393 73252399 CGGGGCTCGGGAGTTCGGGGCCGGGTGGGGAGAGCTCTCCCAGGCGCGATGGAGGCAACCCGAAC CGGGGCTCGGGAGTTCGGGGCCGGGTGGGGA______TCCCAGGCGCGATGGAGGCAACCCGAAC AGAGCTC A MRPS16 Ensembl:ENSG00000182180 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:73252391..73252575 26863196 MeRIP-seq:(Medium) rs1249357464 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_26775030 78724 RMVar_ID_78724 Human_SNP_ID_437658826 m1A Human chr10 - 73252398 73252398 73252398 CGGGGCTCGGGAGTTCGGGGCCGGGTGGGGAGAGCTCTCCCAGGCGCGATGGAGGCAACCCGAAC CGGGGCTCGGGAGTTCGGGGCCGGGTGGGGAGGGCTCTCCCAGGCGCGATGGAGGCAACCCGAAC T C MRPS16 Ensembl:ENSG00000182180 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:73252391..73252575 26863196 MeRIP-seq:(Medium) rs1466598380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26775030 78725 RMVar_ID_78725 Human_SNP_ID_437696728 m1A Human chr10 + 73413899 73413899 73413899 CAAACCGAGTCGCCGCCATCCGGGAGGCCCACACTGCCCTCCAGCCGCGCCCCACTAGCACCGGG CAAACCGAGTCGCCGCCATCCGGGAGGCCCACGCTGCCCTCCAGCCGCGCCCCACTAGCACCGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:73413897..73414031 26863196 MeRIP-seq:(Medium) rs367634977 Functional Loss SNV dbSNP153 33..33 33 - - - 78726 RMVar_ID_78726 Human_SNP_ID_437696738 m1A Human chr10 + 73413944 73413944 73413944 CGCGCCCCACTAGCACCGGGACAGCAGCGCCCAGAGCTGGCCGAGGGCAAGACCACCGAGGCAGA CGCGCCCCACTAGCACCGGGACAGCAGCGCCCGGAGCTGGCCGAGGGCAAGACCACCGAGGCAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:73413939..73414032;chr10:73413943..73414029 26863196 MeRIP-seq:(Medium) rs892779257 Functional Loss SNV dbSNP153 33..33 33 - - - 78727 RMVar_ID_78727 Human_SNP_ID_437723968 m1A Human chr10 - 73523697 73523697 73523697 GTGAACTGGATGAATTGCAGGAAGAGGTGGCCAGGAGGGCGCAGGAACAGGAACTTCGAAGAAAA GTGAACTGGATGAATTGCAGGAAGAGGTGGCCCGGAGGGCGCAGGAACAGGAACTTCGAAGAAAA T G USP54 Ensembl:ENSG00000166348 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:73523582..73523711 26863196 MeRIP-seq:(Medium) rs1484582425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5999109 Human_Splice_Rec_1146466,Human_Splice_Rec_1146482,Human_Splice_Rec_1146510,Human_Splice_Rec_1146548,Human_Splice_Rec_1146584,Human_Splice_Rec_1146596,Human_Splice_Rec_1146634 RMVar_hsa_circ_42724,RMVar_hsa_circ_91450,RMVar_hsa_circ_110450,RMVar_hsa_circ_144318,RMVar_hsa_circ_144319,RMVar_hsa_circ_3773,RMVar_hsa_circ_65447,RMVar_hsa_circ_35904,RMVar_hsa_circ_378301 78728 RMVar_ID_78728 Human_SNP_ID_437725704 m1A Human chr10 + 73530618 73530618 73530618 ATGTCGAAAAAGCAAAGAAAAGCCCTCTGAACAGAAAGGAGAAGCCAACAGTCTGGAGCATGACA ATGTCGAAAAAGCAAAGAAAAGCCCTCTGAACGGAAAGGAGAAGCCAACAGTCTGGAGCATGACA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:73530616..73530748 26863196 MeRIP-seq:(Medium) rs578117418 Functional Loss SNV dbSNP153 33..33 33 - - - 78729 RMVar_ID_78729 Human_SNP_ID_437747727 m1A Human chr10 + 73626160 73626155 73626161 AGGCGTTTCACGGGTGTCCCGGACAGGCGTGGAGGTGGGGCGCAGGCGAGGATGAAGCTTGAGTT AGGCGTTTCACGGGTGTCCCGGACAGGC______GTGGGGCGCAGGCGAGGATGAAGCTTGAGTT CGTGGAG C AC073389.1 Ensembl:ENSG00000268584 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73626110..73626321 26863196 MeRIP-seq:(Medium) rs1239368498 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_5548101 78730 RMVar_ID_78730 Human_SNP_ID_437766224 m1A Human chr10 + 73697818 73697818 73697818 GCCTCTGCTCACAGCTTTGGCCACACACTCCCACTGTCCTAGGCCGAGGCTATGCTGCACTTGCA GCCTCTGCTCACAGCTTTGGCCACACACTCCCGCTGTCCTAGGCCGAGGCTATGCTGCACTTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73697729..73697924 26863196 MeRIP-seq:(Medium) rs1488785680 Functional Loss SNV dbSNP153 33..33 33 - - - 78731 RMVar_ID_78731 Human_SNP_ID_437766242 m1A Human chr10 - 73697870 73697861 73697871 TGCCCGGGGCCGCGCTGTGAGGTGGGCAGGCGAGGAGCGGGAAGACCATCTCTGCAAGTGCAGCA TGCCCGGGGCCGCGCTGTGAGGTGGGCAGGC__________AAGACCATCTCTGCAAGTGCAGCA TCCCGCTCCTC T AC022400.3,AGAP5 Ensembl:ENSG00000242288,Ensembl:ENSG00000172650 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73697848..73697942 26863196 MeRIP-seq:(Medium) rs1565011750 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_8173729 RMVar_hsa_circ_58885,RMVar_hsa_circ_89736,RMVar_hsa_circ_144346,RMVar_hsa_circ_313877 78732 RMVar_ID_78732 Human_SNP_ID_437773167 m1A Human chr10 + 73730427 73730427 73730427 GATCTTCCCAGTGCCCCAAAGCCAGGGACCCCACTGCCGCCTACCCCAGCCCGCGGCACCGAACT GATCTTCCCAGTGCCCCAAAGCCAGGGACCCCGCTGCCGCCTACCCCAGCCCGCGGCACCGAACT A G lnc-SEC24C-3 RNACentral:URS00008B4CE6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73730320..73730454 26863196 MeRIP-seq:(Medium) rs1490248920 Functional Loss SNV dbSNP153 33..33 33 - - - 78733 RMVar_ID_78733 Human_SNP_ID_437773229 m1A Human chr10 - 73730646 73730646 73730646 GAATCGGGAGGGATACGGACCCGGTGGAACGCACTGCGTAGACGGCGCCGGCGCCCGCACTCAGC GAATCGGGAGGGATACGGACCCGGTGGAACGCCCTGCGTAGACGGCGCCGGCGCCCGCACTCAGC T G BMS1P4-AGAP5,BMS1P4-AGAP5:2,BMS1P4-AGAP5:3,BMS1P4-AGAP5:4 RNACentral:URS0000D6E7CF,RNACentral:URS0000D6DEF1,RNACentral:URS0000D6D564,RNACentral:URS0000D6E1FC lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73730597..73730709 26863196 MeRIP-seq:(Medium) rs1468393672 Functional Loss SNV dbSNP153 33..33 33 - - - 78734 RMVar_ID_78734 Human_SNP_ID_437777282 m1A Human chr10 + 73746830 73746830 73746830 CTCACAGGTGAGATCAAATTGGGAATGCTTTCATAATGAACGTCAACCAGTCAGTTCCACCTGTG CTCACAGGTGAGATCAAATTGGGAATGCTTTCGTAATGAACGTCAACCAGTCAGTTCCACCTGTG A G SEC24C Ensembl:ENSG00000176986 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:73746814..73746956 26863196 MeRIP-seq:(Medium) rs761175568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_292393,Human_RBP_ID_382379,Human_RBP_ID_11425873,Human_RBP_ID_17782471,Human_RBP_ID_18432008,Human_RBP_ID_22028592,Human_RBP_ID_22432070,Human_RBP_ID_22788690,Human_RBP_ID_27195043 Human_Splice_Rec_1146878,Human_Splice_Rec_1146922,Human_Splice_Rec_1146966,Human_Splice_Rec_1147010 RMVar_hsa_circ_60050,RMVar_hsa_circ_144367,RMVar_hsa_circ_98684,RMVar_hsa_circ_283658,RMVar_hsa_circ_345883,RMVar_hsa_circ_126838,RMVar_hsa_circ_144368,RMVar_hsa_circ_144369 78735 RMVar_ID_78735 Human_SNP_ID_437777308 m1A Human chr10 + 73746900 73746900 73746900 ATTTGGGCAGCCCCAGCCCATCTACCCAGGGTATCATCAGTCCAGCTATGGTGGGCAATCAGGGT ATTTGGGCAGCCCCAGCCCATCTACCCAGGGTGTCATCAGTCCAGCTATGGTGGGCAATCAGGGT A G SEC24C Ensembl:ENSG00000176986 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73746801..73746900 32194978 MeRIP-seq:(Medium) rs1337384689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_274200,Human_RBP_ID_18187948,Human_RBP_ID_19545871 Human_Splice_Rec_1146878,Human_Splice_Rec_1146922,Human_Splice_Rec_1146966,Human_Splice_Rec_1147010 Human_miRNA_ID_1980709,Human_miRNA_ID_1982433,Human_miRNA_ID_2541883,Human_miRNA_ID_2543757,Human_miRNA_ID_2545607,Human_miRNA_ID_2547462,Human_miRNA_ID_2549326,Human_miRNA_ID_2551195,Human_miRNA_ID_2556602,Human_miRNA_ID_2558484,Human_miRNA_ID_2588903 RMVar_hsa_circ_60050,RMVar_hsa_circ_144367,RMVar_hsa_circ_98684,RMVar_hsa_circ_283658,RMVar_hsa_circ_345883,RMVar_hsa_circ_126838,RMVar_hsa_circ_144368,RMVar_hsa_circ_144369 78736 RMVar_ID_78736 Human_SNP_ID_437780641 m1A Human chr10 + 73760215 73760215 73760215 CAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGACTGGTCCACTCCTGCCTGGACAGAGTTTTGGA CAGCTTCAGGGGGTCCTCGGCTGCCTTCGATGTCTGGTCCACTCCTGCCTGGACAGAGTTTTGGA A T SEC24C Ensembl:ENSG00000176986 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:73760076..73760275 32194978 MeRIP-seq:(Medium) rs555181829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382381,Human_RBP_ID_984426,Human_RBP_ID_4127346,Human_RBP_ID_5999580,Human_RBP_ID_18432009 RMVar_hsa_circ_60050,RMVar_hsa_circ_102979,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369,RMVar_hsa_circ_341521,RMVar_hsa_circ_144371,RMVar_hsa_circ_90199,RMVar_hsa_circ_144370 78737 RMVar_ID_78737 Human_SNP_ID_437783304 m1A Human chr10 + 73769942 73769942 73769942 TGGAGCTGAAGTCACTACTGATGACCGTGCCTATGTCCGACAGCTAGTTACCTCCATGGATGTGA TGGAGCTGAAGTCACTACTGATGACCGTGCCTGTGTCCGACAGCTAGTTACCTCCATGGATGTGA A G SEC24C Ensembl:ENSG00000176986 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73769863..73770014 32194978 MeRIP-seq:(Medium) rs553026455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1449935,Human_RBP_ID_1770620,Human_RBP_ID_5137885,Human_RBP_ID_8338935,Human_RBP_ID_8763081,Human_RBP_ID_9254135,Human_RBP_ID_9273907,Human_RBP_ID_17228198,Human_RBP_ID_17460947,Human_RBP_ID_18970818,Human_RBP_ID_22788702 Human_Splice_Rec_1146915,Human_Splice_Rec_1146959,Human_Splice_Rec_1147003,Human_Splice_Rec_1147047,Human_Splice_Rec_1147071 Human_miRNA_ID_2491452,Human_miRNA_ID_2667094 RMVar_hsa_circ_117895,RMVar_hsa_circ_52481,RMVar_hsa_circ_144375,RMVar_hsa_circ_144376,RMVar_hsa_circ_344411,RMVar_hsa_circ_49765 78738 RMVar_ID_78738 Human_SNP_ID_437783848 m1A Human chr10 + 73771770 73771770 73771770 GGTAGAGGTACCAGCTTCCTTTCCAGCTGGAGAGGCCCCAACACTGGATGGTTCTGTAGGGAGCC GGTAGAGGTACCAGCTTCCTTTCCAGCTGGAGGGGCCCCAACACTGGATGGTTCTGTAGGGAGCC A G SEC24C Ensembl:ENSG00000176986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:73771726..73771775 32194978 MeRIP-seq:(Medium) rs1156770533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382412,Human_RBP_ID_748235,Human_RBP_ID_5313042,Human_RBP_ID_26398430 Human_miRNA_ID_1538823 78739 RMVar_ID_78739 Human_SNP_ID_437784100 m1A Human chr10 + 73772382 73772380 73772382 TTAGGGTGGTGTTGGTCCTTCTAGGGGTGCTCAGTGTCTGTGCAGCCAGCGGCCATGGGTCCGTA TTAGGGTGGTGTTGGTCCTTCTAGGGGTGCT__GTGTCTGTGCAGCCAGCGGCCATGGGTCCGTA TCA T FUT11 Ensembl:ENSG00000196968 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73772332..73772539 26863196 MeRIP-seq:(Medium) rs759791115 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4135893,Human_RBP_ID_8765659 78740 RMVar_ID_78740 Human_SNP_ID_437784102 m1A Human chr10 + 73772382 73772382 73772382 TTAGGGTGGTGTTGGTCCTTCTAGGGGTGCTCAGTGTCTGTGCAGCCAGCGGCCATGGGTCCGTA TTAGGGTGGTGTTGGTCCTTCTAGGGGTGCTCGGTGTCTGTGCAGCCAGCGGCCATGGGTCCGTA A G FUT11 Ensembl:ENSG00000196968 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73772332..73772539 26863196 MeRIP-seq:(Medium) rs369598879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135893,Human_RBP_ID_8765659 78741 RMVar_ID_78741 Human_SNP_ID_437784386 m1A Human chr10 - 73772800 73772800 73772800 GATTGAAGAGGCGGATGCCCGGGCCGTGGCTCAGCAAGAAGTTGTTGAGGGGCGACTCCTCGTGG GATTGAAGAGGCGGATGCCCGGGCCGTGGCTCGGCAAGAAGTTGTTGAGGGGCGACTCCTCGTGG T C AC022400.9 Ensembl:ENSG00000279689 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73772750..73772857 26863196 MeRIP-seq:(Medium) rs1374390271 Functional Loss SNV dbSNP153 33..33 33 - - - 78742 RMVar_ID_78742 Human_SNP_ID_437787039 m1A Human chr10 - 73782104 73782104 73782104 GCACAGGCTTCCGCGGGTTCCCAAACCGCGCCAGACGACCCCGCAGGCTGGGTGTCGCCATAGCG GCACAGGCTTCCGCGGGTTCCCAAACCGCGCCCGACGACCCCGCAGGCTGGGTGTCGCCATAGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:73782051..73782375;chr10:73782051..73782400;chr10:73782051..73782357;chr10:73782051..73782339 26863196 MeRIP-seq:(Medium) rs1007822866 Functional Loss SNV dbSNP153 33..33 33 - - - 78743 RMVar_ID_78743 Human_SNP_ID_437788164 m1A Human chr10 + 73786007 73786007 73786007 GAGGCCGAGAGCCTCTGCCAGAACTGGCGGGGATGGCGCAAACAGTCAGCGGGGCCCAATTCCCC GAGGCCGAGAGCCTCTGCCAGAACTGGCGGGGGTGGCGCAAACAGTCAGCGGGGCCCAATTCCCC A G ZSWIM8 Ensembl:ENSG00000214655 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73785956..73786118 26863196 MeRIP-seq:(Medium) rs762307060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748324,Human_RBP_ID_5520471,Human_RBP_ID_22886645 Human_Splice_Rec_1147091,Human_Splice_Rec_1147141,Human_Splice_Rec_1147193,Human_Splice_Rec_1147243,Human_Splice_Rec_1147293,Human_Splice_Rec_1147343 78744 RMVar_ID_78744 Human_SNP_ID_437789943 m1A Human chr10 + 73792296 73792296 73792296 ACATAAGATGGGTCCAGGTGGGGGCAAAGCCAAGGCACTGGGTGGGGCTGGCAGTGGGAGCAAGG ACATAAGATGGGTCCAGGTGGGGGCAAAGCCAGGGCACTGGGTGGGGCTGGCAGTGGGAGCAAGG A G ZSWIM8 Ensembl:ENSG00000214655 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73792200..73792477 26863196 MeRIP-seq:(Medium) rs1470708718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28386,Human_RBP_ID_259267,Human_RBP_ID_747976,Human_RBP_ID_3937817,Human_RBP_ID_5520138,Human_RBP_ID_8725032,Human_RBP_ID_9273915,Human_RBP_ID_9343601,Human_RBP_ID_18410346,Human_RBP_ID_18970053,Human_RBP_ID_19045444,Human_RBP_ID_21963993,Human_RBP_ID_22029395,Human_RBP_ID_22566237,Human_RBP_ID_22639465,Human_RBP_ID_22708129,Human_RBP_ID_22886647,Human_RBP_ID_24542190,Human_RBP_ID_26316425,Human_RBP_ID_26882201 RMVar_hsa_circ_68581,RMVar_hsa_circ_87559,RMVar_hsa_circ_144382 78745 RMVar_ID_78745 Human_SNP_ID_437789958 m1A Human chr10 + 73792325 73792325 73792325 CCAAGGCACTGGGTGGGGCTGGCAGTGGGAGCAAGGGCTCAGCAGGTGGCGGAAGCAAGCGACGG CCAAGGCACTGGGTGGGGCTGGCAGTGGGAGCCAGGGCTCAGCAGGTGGCGGAAGCAAGCGACGG A C ZSWIM8 Ensembl:ENSG00000214655 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73792228..73792483 26863196 MeRIP-seq:(Medium) rs761070970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28386,Human_RBP_ID_259267,Human_RBP_ID_747976,Human_RBP_ID_806078,Human_RBP_ID_3937817,Human_RBP_ID_5520138,Human_RBP_ID_8228765,Human_RBP_ID_8725032,Human_RBP_ID_9273915,Human_RBP_ID_18410346,Human_RBP_ID_18970053,Human_RBP_ID_19045444,Human_RBP_ID_21963993,Human_RBP_ID_22029395,Human_RBP_ID_22566238,Human_RBP_ID_22639465,Human_RBP_ID_22708129,Human_RBP_ID_22886647,Human_RBP_ID_24542190,Human_RBP_ID_26316425 Human_miRNA_ID_2001728,Human_miRNA_ID_2003112,Human_miRNA_ID_2511951,Human_miRNA_ID_3054769 RMVar_hsa_circ_68581,RMVar_hsa_circ_87559,RMVar_hsa_circ_144382 78746 RMVar_ID_78746 Human_SNP_ID_437790141 m1A Human chr10 + 73792749 73792749 73792749 TGATGACTACCAGGCGTACTATCTGAATGCCCAGGATGGGGCTGGGGGCGAGGAAGAGAAGGCCG TGATGACTACCAGGCGTACTATCTGAATGCCCGGGATGGGGCTGGGGGCGAGGAAGAGAAGGCCG A G ZSWIM8 Ensembl:ENSG00000214655 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73792699..73792850 26863196 MeRIP-seq:(Medium) rs567026375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747977,Human_RBP_ID_8763113,Human_RBP_ID_9360465,Human_RBP_ID_18970054,Human_RBP_ID_22886810,Human_RBP_ID_26317288 Human_miRNA_ID_2040022,Human_miRNA_ID_2468971,Human_miRNA_ID_3019004 RMVar_hsa_circ_68581,RMVar_hsa_circ_87559,RMVar_hsa_circ_144382 78747 RMVar_ID_78747 Human_SNP_ID_437794688 m1A Human chr10 - 73806861 73806861 73806861 GGAAGGTGGTCAGTGTTGTTACAAAATAAAGGAGGGAACAGGGGCTGACTGGCTGTGGTCAGTGG GGAAGGTGGTCAGTGTTGTTACAAAATAAAGGCGGGAACAGGGGCTGACTGGCTGTGGTCAGTGG T G AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73806812..73806949 26863196 MeRIP-seq:(Medium) rs1565098620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2211,Human_RBP_ID_19045458,Human_RBP_ID_21964773 RMVar_hsa_circ_23249,RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928,RMVar_hsa_circ_343725,RMVar_hsa_circ_144392 78748 RMVar_ID_78748 Human_SNP_ID_437795101 m1A Human chr10 - 73808163 73808163 73808163 CTGCACGGCCTCCAGTTCCACCTCGGCCCCCCAGGCCTCCAGAGACAGCTCGAACTGAACCCGTG CTGCACGGCCTCCAGTTCCACCTCGGCCCCCCGGGCCTCCAGAGACAGCTCGAACTGAACCCGTG T C AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:73808115..73808200 26863196 MeRIP-seq:(Medium) rs1258248369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27407174 Human_miRNA_ID_2792763 RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928,RMVar_hsa_circ_343725,RMVar_hsa_circ_53246,RMVar_hsa_circ_144392 78749 RMVar_ID_78749 Human_SNP_ID_437796017 m1A Human chr10 - 73811564 73811564 73811564 AGCGTTCGCTCGGAGATGGCGGAGCAGCCGCGACGCGGCCCGTGGCCCCGAAAGCAGGGAAGCCG AGCGTTCGCTCGGAGATGGCGGAGCAGCCGCGTCGCGGCCCGTGGCCCCGAAAGCAGGGAAGCCG T A AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73811516..73811747 26863196 MeRIP-seq:(Medium) rs1282232303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136843,Human_RBP_ID_5415285,Human_RBP_ID_5520146 Human_Splice_Rec_1147595,Human_Splice_Rec_1147657,Human_Splice_Rec_1147693 78750 RMVar_ID_78750 Human_SNP_ID_437802420 m1A Human chr10 - 73834927 73834927 73834927 TCTTCTTTATGGCTGAAGGGAAGAGCAATTGCATAAAATGAGACCTGAAATAAAGCAGTGACTGT TCTTCTTTATGGCTGAAGGGAAGAGCAATTGCGTAAAATGAGACCTGAAATAAAGCAGTGACTGT T C CAMK2G Ensembl:ENSG00000148660 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73834923..73835165 26863196 MeRIP-seq:(Medium) rs1159963551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2760,RMVar_hsa_circ_121524,RMVar_hsa_circ_23021,RMVar_hsa_circ_144393,RMVar_hsa_circ_290614,RMVar_hsa_circ_144395,RMVar_hsa_circ_17596,RMVar_hsa_circ_372629,RMVar_hsa_circ_144398,RMVar_hsa_circ_22406 78751 RMVar_ID_78751 Human_SNP_ID_437812025 m1A Human chr10 - 73874446 73874446 73874446 TCCGCCCGCCCGCCAGCATGGCCACCACCGCCACCTGCACCCGTTTCACCGACGACTACCAGCTC TCCGCCCGCCCGCCAGCATGGCCACCACCGCCCCCTGCACCCGTTTCACCGACGACTACCAGCTC T G CAMK2G Ensembl:ENSG00000148660 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:73874343..73874499;chr10:73874381..73874530 26863196 MeRIP-seq:(Medium) rs780866920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136375 Human_Splice_Rec_1147695,Human_Splice_Rec_1147731,Human_Splice_Rec_1147771,Human_Splice_Rec_1147811,Human_Splice_Rec_1147851,Human_Splice_Rec_1147925,Human_Splice_Rec_1147965,Human_Splice_Rec_1148027 78752 RMVar_ID_78752 Human_SNP_ID_437812042 m1A Human chr10 + 73874501 73874480 73874501 GGCGGGCGGACGCGGCGGTGCAGCCCGCGCCGACGTCGGTGCACAGTCACCGCCGCCCGGCCGAG GGCGGGCGGACG_____________________CGTCGGTGCACAGTCACCGCCGCCCGGCCGAG GCGGCGGTGCAGCCCGCGCCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73874332..73874525 26863196 MeRIP-seq:(Medium) rs1478411216 Functional Loss DEL dbSNP153 13..33 33 - - - 78753 RMVar_ID_78753 Human_SNP_ID_437815721 m1A Human chr10 - 73889416 73889416 73889416 AAGAGAAAGAAAGAAGGAAAGAAAAGAAAACAAAAGAGCTGGATGAGAAAGTTCTAAAGGTAGAG AAGAGAAAGAAAGAAGGAAAGAAAAGAAAACAGAAGAGCTGGATGAGAAAGTTCTAAAGGTAGAG T C MG828475 RNACentral:URS0000E46FEA lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:73889246..73889456;chr10:73889264..73889426 26863196 MeRIP-seq:(Medium) rs977603541 Functional Loss SNV dbSNP153 33..33 33 - - - 78754 RMVar_ID_78754 Human_SNP_ID_437867153 m1A Human chr10 - 74107298 74107298 74107298 AGGCGGCGGGAAGTCAGGCTCCTGAGGTTGGAAGGCTTCTCTGACCTTGGCCACAGCTCCCAGGA AGGCGGCGGGAAGTCAGGCTCCTGAGGTTGGACGGCTTCTCTGACCTTGGCCACAGCTCCCAGGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:74107247..74107350 32194978 MeRIP-seq:(Medium) rs1179660936 Functional Loss SNV dbSNP153 33..33 33 - - - 78755 RMVar_ID_78755 Human_SNP_ID_437868789 m1A Human chr10 - 74114324 74114324 74114324 GTGCACTGCTTGGCAACCTCCTTGGCCAACCGAGTCACCTCATCTGAGGCCTTGGCGATGTCCTT GTGCACTGCTTGGCAACCTCCTTGGCCAACCGCGTCACCTCATCTGAGGCCTTGGCGATGTCCTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:74114276..74114400 32194978 MeRIP-seq:(Medium) rs779689114 Functional Loss SNV dbSNP153 33..33 33 - - - 78756 RMVar_ID_78756 Human_SNP_ID_437869846 m1A Human chr10 - 74119124 74119124 74119124 GAGACATGTTTTGGTTAAAATTAAAATGCAGCATTTCAGCTCAAAATGAACAATTAAGAGCTAAG GAGACATGTTTTGGTTAAAATTAAAATGCAGCGTTTCAGCTCAAAATGAACAATTAAGAGCTAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:74118964..74119165 32194978 MeRIP-seq:(Medium) rs1287285851 Functional Loss SNV dbSNP153 33..33 33 - - - 78757 RMVar_ID_78757 Human_SNP_ID_437869847 m1A Human chr10 - 74119124 74119124 74119124 GAGACATGTTTTGGTTAAAATTAAAATGCAGCATTTCAGCTCAAAATGAACAATTAAGAGCTAAG GAGACATGTTTTGGTTAAAATTAAAATGCAGCCTTTCAGCTCAAAATGAACAATTAAGAGCTAAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:74118964..74119165 32194978 MeRIP-seq:(Medium) rs1287285851 Functional Loss SNV dbSNP153 33..33 33 - - - 78758 RMVar_ID_78758 Human_SNP_ID_437877738 m1A Human chr10 + 74151279 74151265 74151279 CTGTAGAGCCAAAGTGGGGTGGGAGCGCGAAGATGGCAGCTGCTGAGGAGGAGCCGAAGCCCAAA CTGTAGAGCCAAAGTGGGG______________TGGCAGCTGCTGAGGAGGAGCCGAAGCCCAAA GTGGGAGCGCGAAGA G ADK Ensembl:ENSG00000156110 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:74151196..74151407;chr10:74151201..74151391 26863196 MeRIP-seq:(Medium) rs1347525545 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_862479,Human_RBP_ID_3937865,Human_RBP_ID_4128073,Human_RBP_ID_18416134,Human_RBP_ID_18970080,Human_RBP_ID_22029409,Human_RBP_ID_26316445,Human_RBP_ID_27802158 Human_Splice_Rec_1148399,Human_Splice_Rec_1148417,Human_Splice_Rec_1148437,Human_Splice_Rec_1148459,Human_Splice_Rec_1148465 78759 RMVar_ID_78759 Human_SNP_ID_437877748 m1A Human chr10 + 74151279 74151279 74151279 CTGTAGAGCCAAAGTGGGGTGGGAGCGCGAAGATGGCAGCTGCTGAGGAGGAGCCGAAGCCCAAA CTGTAGAGCCAAAGTGGGGTGGGAGCGCGAAGGTGGCAGCTGCTGAGGAGGAGCCGAAGCCCAAA A G ADK Ensembl:ENSG00000156110 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:74151196..74151407;chr10:74151201..74151391 26863196 MeRIP-seq:(Medium) rs527871671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862479,Human_RBP_ID_3937865,Human_RBP_ID_4128073,Human_RBP_ID_18416134,Human_RBP_ID_18970080,Human_RBP_ID_22029409,Human_RBP_ID_26316445,Human_RBP_ID_27802158 Human_Splice_Rec_1148399,Human_Splice_Rec_1148417,Human_Splice_Rec_1148437,Human_Splice_Rec_1148459,Human_Splice_Rec_1148465 78760 RMVar_ID_78760 Human_SNP_ID_437877749 m1A Human chr10 - 74151280 74151280 74151280 TTTTGGGCTTCGGCTCCTCCTCAGCAGCTGCCATCTTCGCGCTCCCACCCCACTTTGGCTCTACA TTTTGGGCTTCGGCTCCTCCTCAGCAGCTGCCTTCTTCGCGCTCCCACCCCACTTTGGCTCTACA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:74151194..74151369;chr10:74151192..74151626 26863196 MeRIP-seq:(Medium) rs201678543 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 78761 RMVar_ID_78761 Human_SNP_ID_437877750 m1A Human chr10 - 74151280 74151280 74151280 TTTTGGGCTTCGGCTCCTCCTCAGCAGCTGCCATCTTCGCGCTCCCACCCCACTTTGGCTCTACA TTTTGGGCTTCGGCTCCTCCTCAGCAGCTGCCGTCTTCGCGCTCCCACCCCACTTTGGCTCTACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:74151194..74151369;chr10:74151192..74151626 26863196 MeRIP-seq:(Medium) rs201678543 Functional Loss SNV dbSNP153 33..33 33 - - - 78762 RMVar_ID_78762 Human_SNP_ID_437889402 m1A Human chr10 + 74200815 74200815 74200815 ATGGGAAATCCTCTGCTTGACATCTCTGCTGTAGTGGACAAAGATTTCCTTGATAAGTAAGTATT ATGGGAAATCCTCTGCTTGACATCTCTGCTGTGGTGGACAAAGATTTCCTTGATAAGTAAGTATT A G ADK Ensembl:ENSG00000156110 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:74176773..74224548 32194978 MeRIP-seq:(Medium) rs1456457845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27867,Human_RBP_ID_382698,Human_RBP_ID_1262038,Human_RBP_ID_1770732,Human_RBP_ID_3937866,Human_RBP_ID_8339139,Human_RBP_ID_18970081,Human_RBP_ID_22886757,Human_RBP_ID_26315942,Human_RBP_ID_27802159 Human_Splice_Rec_1148400,Human_Splice_Rec_1148401,Human_Splice_Rec_1148418,Human_Splice_Rec_1148419,Human_Splice_Rec_1148438,Human_Splice_Rec_1148439,Human_Splice_Rec_1148462,Human_Splice_Rec_1148463,Human_Splice_Rec_1148466,Human_Splice_Rec_1148467,Human_Splice_Rec_1148484,Human_Splice_Rec_1148485,Human_Splice_Rec_1148506,Human_Splice_Rec_1148507,Human_Splice_Rec_1148526,Human_Splice_Rec_1148527,Human_Splice_Rec_1148548,Human_Splice_Rec_1148549,Human_Splice_Rec_1148570,Human_Splice_Rec_1148571,Human_Splice_Rec_1148588,Human_Splice_Rec_1148589 RMVar_hsa_circ_54682,RMVar_hsa_circ_89295,RMVar_hsa_circ_316501,RMVar_hsa_circ_330370,RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144420,RMVar_hsa_circ_144421,RMVar_hsa_circ_144422 78763 RMVar_ID_78763 Human_SNP_ID_438032869 m1A Human chr10 + 74825555 74825555 74825555 GGAGGCGGCGGCGGTGGGTCCCGGGCGGGGGGAGCGCGGCGCTGCGGACCCGGGCGGCTGGCAAA GGAGGCGGCGGCGGTGGGTCCCGGGCGGGGGGGGCGCGGCGCTGCGGACCCGGGCGGCTGGCAAA A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:74825410..74825870 26863196 MeRIP-seq:(Medium) rs1462616260 Functional Loss SNV dbSNP153 33..33 33 - - - 78764 RMVar_ID_78764 Human_SNP_ID_438032891 m1A Human chr10 + 74825626 74825626 74825626 GGCGGAGGCTGAGGAAGGCAGCGGGGAGACCCAGGCTGCAGCAACAAAGGGCAGCGAGCGATTGG GGCGGAGGCTGAGGAAGGCAGCGGGGAGACCCGGGCTGCAGCAACAAAGGGCAGCGAGCGATTGG A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:74825431..74825830 26863196 MeRIP-seq:(Medium) rs1011043249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862480 Human_Splice_Rec_1148735,Human_Splice_Rec_1148769,Human_Splice_Rec_1148801,Human_Splice_Rec_1148829,Human_Splice_Rec_1148863,Human_Splice_Rec_1148893,Human_Splice_Rec_1148899 78765 RMVar_ID_78765 Human_SNP_ID_438033249 m1A Human chr10 - 74826666 74826666 74826666 CCTCCGCCACCGCTGCCGCCGCCGCCAGGGGTAGGAGCTAAGCCGCCGCCATTTTGTGTCCCCCT CCTCCGCCACCGCTGCCGCCGCCGCCAGGGGTGGGAGCTAAGCCGCCGCCATTTTGTGTCCCCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:74826405..74826812 26863196 MeRIP-seq:(Medium) rs1291163835 Functional Loss SNV dbSNP153 33..33 33 - - - 78766 RMVar_ID_78766 Human_SNP_ID_438036415 m1A Human chr10 + 74838614 74838614 74838614 TGGAGCTGTTTGTCTTGAATGGTTGTGGAGATACACGGATGGTTGCTGAATTTAAGGATGTCCTT TGGAGCTGTTTGTCTTGAATGGTTGTGGAGATGCACGGATGGTTGCTGAATTTAAGGATGTCCTT A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:74838611..74838706 26863196 MeRIP-seq:(Medium) rs1298808353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18598426 78767 RMVar_ID_78767 Human_SNP_ID_438071771 m1A Human chr10 + 74997321 74997321 74997321 AGGACAGGAACACAGAATGTACAGAAAAGGAAAATCACTGGTGGCCACGACATTGCTGACATTTA AGGACAGGAACACAGAATGTACAGAAAAGGAATATCACTGGTGGCCACGACATTGCTGACATTTA A T KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:74997240..74997324 26863410 MeRIP-seq:(Medium) rs1237210716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19549749 RMVar_hsa_circ_144441,RMVar_hsa_circ_125164,RMVar_hsa_circ_15495,RMVar_hsa_circ_17668,RMVar_hsa_circ_323227,RMVar_hsa_circ_144452,RMVar_hsa_circ_364394,RMVar_hsa_circ_57757,RMVar_hsa_circ_4471 78768 RMVar_ID_78768 Human_SNP_ID_438072222 m1A Human chr10 - 74999387 74999387 74999387 TCACCCACATCCATGGTTTCAGCTACCACCGCATGTCCACGACTCCCAGCTGCTCCCTCTAATGC TCACCCACATCCATGGTTTCAGCTACCACCGCGTGTCCACGACTCCCAGCTGCTCCCTCTAATGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:74999377..74999493 26863196 MeRIP-seq:(Medium) rs1470477175 Functional Loss SNV dbSNP153 33..33 33 - - - 78769 RMVar_ID_78769 Human_SNP_ID_608812673 m1A Human chr16 + 75110399 75110399 75110399 AGGTTCTACCCTCTCTGCTAAGGGCCTAGCACACTTTGATGAGGTTCCTGGACGTGAGACCCTCA AGGTTCTACCCTCTCTGCTAAGGGCCTAGCACGCTTTGATGAGGTTCCTGGACGTGAGACCCTCA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1043503 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9496,GWAS_ID_9497 78770 RMVar_ID_78770 Human_SNP_ID_608812674 m1A Human chr16 + 75110399 75110399 75110399 AGGTTCTACCCTCTCTGCTAAGGGCCTAGCACACTTTGATGAGGTTCCTGGACGTGAGACCCTCA AGGTTCTACCCTCTCTGCTAAGGGCCTAGCACTCTTTGATGAGGTTCCTGGACGTGAGACCCTCA A T ZNRF1 Ensembl:ENSG00000186187 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1043503 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9496,GWAS_ID_9497 78771 RMVar_ID_78771 Human_SNP_ID_608813394 m1A Human chr16 - 75112473 75112473 75112473 CACGGAACGTGCACGGGGGAGCATGGCATCGGAATGGGCAAGCGGCAGCTGCTGCAGGAGGAGGT CACGGAACGTGCACGGGGGAGCATGGCATCGGGATGGGCAAGCGGCAGCTGCTGCAGGAGGAGGT T C LDHD Ensembl:ENSG00000166816 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75112391..75112698 26863196 MeRIP-seq:(Medium) rs1157566125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1740646,Human_Splice_Rec_1740666,Human_Splice_Rec_1740686 78772 RMVar_ID_78772 Human_SNP_ID_608826143 m1A Human chr16 - 75148891 75148891 75148891 GCCGCCCGTCTGAGGCGCATCTCCTGACAAAGAGAAGAAGGCGAAGCCTCATAGCCGCCCTTCCC GCCGCCCGTCTGAGGCGCATCTCCTGACAAAGTGAAGAAGGCGAAGCCTCATAGCCGCCCTTCCC T A lnc-LDHD-3 RNACentral:URS0000D578F2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75148885..75149099 26863196 MeRIP-seq:(Medium) rs984776306 Functional Loss SNV dbSNP153 33..33 33 - - - 78773 RMVar_ID_78773 Human_SNP_ID_608826144 m1A Human chr16 - 75148891 75148891 75148891 GCCGCCCGTCTGAGGCGCATCTCCTGACAAAGAGAAGAAGGCGAAGCCTCATAGCCGCCCTTCCC GCCGCCCGTCTGAGGCGCATCTCCTGACAAAGGGAAGAAGGCGAAGCCTCATAGCCGCCCTTCCC T C lnc-LDHD-3 RNACentral:URS0000D578F2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75148885..75149099 26863196 MeRIP-seq:(Medium) rs984776306 Functional Loss SNV dbSNP153 33..33 33 - - - 78774 RMVar_ID_78774 Human_SNP_ID_608861206 m1A Human chr16 - 75235746 75235746 75235746 TGCCCCCTGGCTTGCGGCGGCCTGGCCCGGGCACCCTGTACGATGTGCCCCGTGAACGGGTGCTT TGCCCCCTGGCTTGCGGCGGCCTGGCCCGGGCGCCCTGTACGATGTGCCCCGTGAACGGGTGCTT T C BCAR1 Ensembl:ENSG00000050820 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:75235699..75235907 26863196 MeRIP-seq:(Medium) rs1440214765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9286415,Human_RBP_ID_27445683 Human_miRNA_ID_2718941 RMVar_hsa_circ_50858,RMVar_hsa_circ_341658,RMVar_hsa_circ_180058,RMVar_hsa_circ_316723 78775 RMVar_ID_78775 Human_SNP_ID_608863826 m1A Human chr16 + 75242590 75242590 75242590 GGCACCTGGTAAATATCCTGGGCAGGGCCTCCAGGCCCTGGGGGCACCTGGTACAGGTCTGTGGC GGCACCTGGTAAATATCCTGGGCAGGGCCTCCGGGCCCTGGGGGCACCTGGTACAGGTCTGTGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:75242543..75242793 32194978 MeRIP-seq:(Medium) rs1275800171 Functional Loss SNV dbSNP153 33..33 33 - - - 78776 RMVar_ID_78776 Human_SNP_ID_608866597 m1A Human chr16 - 75250652 75250652 75250652 TGATCGCTGGACCGAGGTGAGGGAGTTGGGAAAGCGGAGATTTGCCTAGGGGTGCGGGGTGAGGG TGATCGCTGGACCGAGGTGAGGGAGTTGGGAAGGCGGAGATTTGCCTAGGGGTGCGGGGTGAGGG T C BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:75250649..75251815 26863196 MeRIP-seq:(Medium) rs1017088402 Functional Loss SNV dbSNP153 33..33 33 - - - 78777 RMVar_ID_78777 Human_SNP_ID_608868988 m1A Human chr16 - 75258134 75258134 75258134 GGTAGGCCAAGGGAAGGTGCGCCCTGGTGCCCAGCGGGGTGGGGCCAGTGTGTGATGGCGCAGGG GGTAGGCCAAGGGAAGGTGCGCCCTGGTGCCCGGCGGGGTGGGGCCAGTGTGTGATGGCGCAGGG T C BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:75258132..75258299 26863196 MeRIP-seq:(Medium) rs1297015683 Functional Loss SNV dbSNP153 33..33 33 - - - 78778 RMVar_ID_78778 Human_SNP_ID_608871310 m1A Human chr16 - 75265928 75265928 75265928 CTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGACCCCTCGCGGGGCCTCTGAGCGGCGCGGGCGG CTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGGCCCCTCGCGGGGCCTCTGAGCGGCGCGGGCGG T C BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:75265213..75266000;chr16:75265213..75265975;chr16:75265779..75265975 26863196 MeRIP-seq:(Medium) rs1443236856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393257,Human_RBP_ID_22944891 78779 RMVar_ID_78779 Human_SNP_ID_608871315 m1A Human chr16 - 75265945 75265945 75265945 TCCGGCGTCCGGGAACGCTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGACCCCTCGCGGGGCCT TCCGGCGTCCGGGAACGCTCAGGAGCCGGAGGTGCCGGAAAGCGCCGGGACCCCTCGCGGGGCCT T A BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:75265826..75265975 26863196 MeRIP-seq:(Medium) rs912006323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393999,Human_RBP_ID_22944891 78780 RMVar_ID_78780 Human_SNP_ID_608871325 m1A Human chr16 - 75265957 75265957 75265957 GCGGCCGGACAGTCCGGCGTCCGGGAACGCTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGACCC GCGGCCGGACAGTCCGGCGTCCGGGAACGCTCGGGAGCCGGAGGAGCCGGAAAGCGCCGGGACCC T C BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:75265862..75265964 26863410 MeRIP-seq:(Medium) rs921736856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384405,Human_RBP_ID_22944891 78781 RMVar_ID_78781 Human_SNP_ID_608889590 m1A Human chr16 - 75326193 75326193 75326193 TCGCCAGTGTCAAGGGGAAAAACTCATTTGGCACACAAAAGTCTTTCATTAGGTCCCCTGACTTG TCGCCAGTGTCAAGGGGAAAAACTCATTTGGCGCACAAAAGTCTTTCATTAGGTCCCCTGACTTG T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75326187..75326254 26863196 MeRIP-seq:(Medium) rs1386064271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180059 78782 RMVar_ID_78782 Human_SNP_ID_608908637 m1A Human chr16 + 75390446 75390446 75390446 ATATCTGATCACACTACCCTGCCTTGAGCAAGAATCACCCTCTCCTTGATGTCTCCTCTTAGTAA ATATCTGATCACACTACCCTGCCTTGAGCAAGTATCACCCTCTCCTTGATGTCTCCTCTTAGTAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75390440..75390549 26863196 MeRIP-seq:(Medium) rs938271317 Functional Loss SNV dbSNP153 33..33 33 - - - 78783 RMVar_ID_78783 Human_SNP_ID_608916142 m1A Human chr16 - 75412621 75412621 75412621 AGCAGGAAAAAGGCATTGGATCAGAGGATGCCAGGAAAAAGAAGGAGGACGAACTCTGGGCCAGC AGCAGGAAAAAGGCATTGGATCAGAGGATGCCTGGAAAAAGAAGGAGGACGAACTCTGGGCCAGC T A CFDP1 Ensembl:ENSG00000153774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75412573..75412807 26863196 MeRIP-seq:(Medium) rs1272725243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45028,Human_RBP_ID_479639,Human_RBP_ID_892618,Human_RBP_ID_18684690,Human_RBP_ID_22945142,Human_RBP_ID_24544418,Human_RBP_ID_26328240,Human_RBP_ID_27811283 Human_Splice_Rec_1740973,Human_Splice_Rec_1741001,Human_Splice_Rec_1741007,Human_Splice_Rec_1741015 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_62140,RMVar_hsa_circ_180066,RMVar_hsa_circ_180067,RMVar_hsa_circ_312389,RMVar_hsa_circ_367494,RMVar_hsa_circ_303150,RMVar_hsa_circ_377145 78784 RMVar_ID_78784 Human_SNP_ID_608916802 m1A Human chr16 - 75414613 75414613 75414613 GTGGATGGTGAAGAGCAGACACAGAAAACCCAAGGGAAAAAAAGAAAGGCCCAGAGCATTCCAGC GTGGATGGTGAAGAGCAGACACAGAAAACCCAGGGGAAAAAAAGAAAGGCCCAGAGCATTCCAGC T C AC009163.5,CFDP1 Ensembl:ENSG00000261717,Ensembl:ENSG00000153774 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:75414592..75414782 26863196 MeRIP-seq:(Medium) rs1226333823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5870,Human_RBP_ID_895461,Human_RBP_ID_2483222,Human_RBP_ID_3949591,Human_RBP_ID_9373244,Human_RBP_ID_22942285,Human_RBP_ID_24544421,Human_RBP_ID_26329248,Human_RBP_ID_27811992 Human_Splice_Rec_1740970,Human_Splice_Rec_1740971,Human_Splice_Rec_1740998,Human_Splice_Rec_1740999,Human_Splice_Rec_1741012,Human_Splice_Rec_1741013,Human_Splice_Rec_1741022,Human_Splice_Rec_1741030,Human_Splice_Rec_1741031,Human_Splice_Rec_1741036,Human_Splice_Rec_1741037 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_116551,RMVar_hsa_circ_180066,RMVar_hsa_circ_180067,RMVar_hsa_circ_312389,RMVar_hsa_circ_377145,RMVar_hsa_circ_180068 78785 RMVar_ID_78785 Human_SNP_ID_608916828 m1A Human chr16 - 75414679 75414679 75414679 TGTTATGTGATTTCAGGTGGAGAGTATAGTGAAGATGATGTAAATGAATTAGTGAAGGAAGATGA TGTTATGTGATTTCAGGTGGAGAGTATAGTGAGGATGATGTAAATGAATTAGTGAAGGAAGATGA T C AC009163.5,CFDP1 Ensembl:ENSG00000261717,Ensembl:ENSG00000153774 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:75411920..75419044;chr16:75406695..75419044;chr16:75406695..75464625 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1425137659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3949591,Human_RBP_ID_9373246,Human_RBP_ID_21889411,Human_RBP_ID_23700575,Human_RBP_ID_24544548,Human_RBP_ID_26330285,Human_RBP_ID_27811285 Human_Splice_Rec_1740970,Human_Splice_Rec_1740998,Human_Splice_Rec_1741012,Human_Splice_Rec_1741022,Human_Splice_Rec_1741030,Human_Splice_Rec_1741036 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_116551,RMVar_hsa_circ_180066,RMVar_hsa_circ_180067,RMVar_hsa_circ_312389,RMVar_hsa_circ_377145,RMVar_hsa_circ_180068 78786 RMVar_ID_78786 Human_SNP_ID_608923620 m1A Human chr16 + 75433430 75433430 75433430 CGCCTCCAACGGCAAAGCTCTAGGGAGAGACCATAGAGCCCCGGCGGCGGCGACGGCAGCTAGGG CGCCTCCAACGGCAAAGCTCTAGGGAGAGACCGTAGAGCCCCGGCGGCGGCGACGGCAGCTAGGG A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:75433336..75433436 32194978 MeRIP-seq:(Medium) rs1232714693 Functional Loss SNV dbSNP153 33..33 33 - - - 78787 RMVar_ID_78787 Human_SNP_ID_608929425 m1A Human chr16 - 75451841 75451841 75451841 GTGATTCACAACTTTTCTTTGTCTTCCCTCATAGAGATGTGGTATGGTGTATTCCTGTGGGCACT GTGATTCACAACTTTTCTTTGTCTTCCCTCATGGAGATGTGGTATGGTGTATTCCTGTGGGCACT T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75451804..75451876 26863196 MeRIP-seq:(Medium) rs1285749488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283287,Human_RBP_ID_25240761 78788 RMVar_ID_78788 Human_SNP_ID_608933725 m1A Human chr16 + 75464567 75464567 75464567 CAGGCTCAGGATCTGCTGCAGGAGCCCGGCCGACCCGCCGCTGCCGCCGCTCCCCTCGCGCTCCA CAGGCTCAGGATCTGCTGCAGGAGCCCGGCCGCCCCGCCGCTGCCGCCGCTCCCCTCGCGCTCCA A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75464516..75464690 26863196 MeRIP-seq:(Medium) rs752230193 Functional Loss SNV dbSNP153 33..33 33 - - - 78789 RMVar_ID_78789 Human_SNP_ID_608933799 m1A Human chr16 + 75464666 75464666 75464666 GAGCGCCCGAAGTGCGGTAGCGGCCGGCGCCGACTCACCCTCGCCGCCTCAGCGTCACCTCCAGC GAGCGCCCGAAGTGCGGTAGCGGCCGGCGCCGCCTCACCCTCGCCGCCTCAGCGTCACCTCCAGC A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:75464445..75464704;chr16:75464500..75464706;chr16:75464506..75464700 26863196 MeRIP-seq:(Medium) rs965020303 Functional Loss SNV dbSNP153 33..33 33 - - - 78790 RMVar_ID_78790 Human_SNP_ID_608949612 m1A Human chr16 + 75516510 75516510 75516510 TGCCTCCCCTCAAAGCTTTTCTCCTCCTTCCCAGGTGAAGTCCTCTCTCCTCCCTCCAGCTTTCA TGCCTCCCCTCAAAGCTTTTCTCCTCCTTCCCCGGTGAAGTCCTCTCTCCTCCCTCCAGCTTTCA A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75516416..75516554 26863196 MeRIP-seq:(Medium) rs1159647664 Functional Loss SNV dbSNP153 33..33 33 - - - 78791 RMVar_ID_78791 Human_SNP_ID_608965667 m1A Human chr16 - 75566418 75566415 75566418 GCCGCGGAGCTCAGCGCACCGAGCACAACAACAACGACGGCGGCAGCGGCAGCGGCAGCGACGGC GCCGCGGAGCTCAGCGCACCGAGCACAACAAC___GACGGCGGCAGCGGCAGCGGCAGCGACGGC CGTT C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:75566384..75566480 26863410 MeRIP-seq:(Medium) rs1198859844 Functional Loss DEL dbSNP153 33..35 33 - - - 78792 RMVar_ID_78792 Human_SNP_ID_608965669 m1A Human chr16 - 75566418 75566418 75566418 GCCGCGGAGCTCAGCGCACCGAGCACAACAACAACGACGGCGGCAGCGGCAGCGGCAGCGACGGC GCCGCGGAGCTCAGCGCACCGAGCACAACAACGACGACGGCGGCAGCGGCAGCGGCAGCGACGGC T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:75566384..75566480 26863410 MeRIP-seq:(Medium) rs1347760095 Functional Loss SNV dbSNP153 33..33 33 - - - 78793 RMVar_ID_78793 Human_SNP_ID_608965670 m1A Human chr16 - 75566418 75566418 75566418 GCCGCGGAGCTCAGCGCACCGAGCACAACAACAACGACGGCGGCAGCGGCAGCGGCAGCGACGGC GCCGCGGAGCTCAGCGCACCGAGCACAACAACCACGACGGCGGCAGCGGCAGCGGCAGCGACGGC T G AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:75566384..75566480 26863410 MeRIP-seq:(Medium) rs1347760095 Functional Loss SNV dbSNP153 33..33 33 - - - 78794 RMVar_ID_78794 Human_SNP_ID_608965706 m1A Human chr16 - 75566468 75566468 75566468 AACATCCACTTCATGGCGGCGGCGGGAAGGGGACGGAACCGGCTCGCGGAGCCGCGGAGCTCAGC AACATCCACTTCATGGCGGCGGCGGGAAGGGGGCGGAACCGGCTCGCGGAGCCGCGGAGCTCAGC T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:75566376..75566550 26863410 MeRIP-seq:(Medium) rs769994832 Functional Loss SNV dbSNP153 33..33 33 - - - 78795 RMVar_ID_78795 Human_SNP_ID_608971033 m1A Human chr16 + 75585382 75585382 75585382 TTCCCTCTAAACTGTTGCCAAATGTACCCCCAATTCTTTTTGCTTGCTAGCCACTAATATTTCCC TTCCCTCTAAACTGTTGCCAAATGTACCCCCAGTTCTTTTTGCTTGCTAGCCACTAATATTTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75585332..75585397 26863196 MeRIP-seq:(Medium) rs1011615437 Functional Loss SNV dbSNP153 33..33 33 - - - 78796 RMVar_ID_78796 Human_SNP_ID_608982115 m1A Human chr16 + 75620725 75620725 75620725 GCTGCCAATAATGTCCACTCATGGTTTGGCTCAGGCTTCCCCTTCTTGGGCAGCCTGATCCCATA GCTGCCAATAATGTCCACTCATGGTTTGGCTCGGGCTTCCCCTTCTTGGGCAGCCTGATCCCATA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:75620676..75620750 32194978 MeRIP-seq:(Medium) rs1231961623 Functional Loss SNV dbSNP153 33..33 33 - - - 78797 RMVar_ID_78797 Human_SNP_ID_608986783 m1A Human chr16 + 75634291 75634291 75634291 CCCCTGGGATGATGTTCATCATGGGAGTTTCAATCTAAAAAAGGCAGGGAGAAACATCAGTCCTT CCCCTGGGATGATGTTCATCATGGGAGTTTCAGTCTAAAAAAGGCAGGGAGAAACATCAGTCCTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:75634151..75635338 32194978 MeRIP-seq:(Medium) rs762673443 Functional Loss SNV dbSNP153 33..33 33 - - - 78798 RMVar_ID_78798 Human_SNP_ID_608987346 m1A Human chr16 - 75636022 75636022 75636022 TGCGTCGGGGAGACATAATTGGAGTTCAGGGGAATCCTGGTAAAACCAAGAAGGGTGAGCTGAGC TGCGTCGGGGAGACATAATTGGAGTTCAGGGGCATCCTGGTAAAACCAAGAAGGGTGAGCTGAGC T G KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75635971..75636041 26863196 MeRIP-seq:(Medium) rs1300293815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479831,Human_RBP_ID_1846881,Human_RBP_ID_17883575,Human_RBP_ID_18190097,Human_RBP_ID_26949608,Human_RBP_ID_27246176,Human_RBP_ID_27660512 Human_Splice_Rec_1741318,Human_Splice_Rec_1741344,Human_Splice_Rec_1741374,Human_Splice_Rec_1741398,Human_Splice_Rec_1741412,Human_Splice_Rec_1741422,Human_Splice_Rec_1741438,Human_Splice_Rec_1741450 Human_miRNA_ID_2278424 RMVar_hsa_circ_19457,RMVar_hsa_circ_94319,RMVar_hsa_circ_83265,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086,RMVar_hsa_circ_180089,RMVar_hsa_circ_180088,RMVar_hsa_circ_44041,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_352227,RMVar_hsa_circ_55277,RMVar_hsa_circ_361949,RMVar_hsa_circ_331020,RMVar_hsa_circ_180091 78799 RMVar_ID_78799 Human_SNP_ID_608988894 m1A Human chr16 - 75640304 75640304 75640304 TCCGCAGTCAAGCAATTCATCAGCTGAAGGTCAATGGGGAAGACCCATACCCACACAAGTTCCAT TCCGCAGTCAAGCAATTCATCAGCTGAAGGTCGATGGGGAAGACCCATACCCACACAAGTTCCAT T C KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75640254..75640394 26863196 MeRIP-seq:(Medium) rs369759907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43690,Human_RBP_ID_1523058,Human_RBP_ID_1846885,Human_RBP_ID_4384790,Human_RBP_ID_9065665,Human_RBP_ID_17256177,Human_RBP_ID_26811558 Human_Splice_Rec_1741314,Human_Splice_Rec_1741340,Human_Splice_Rec_1741408,Human_Splice_Rec_1741434,Human_Splice_Rec_1741446,Human_Splice_Rec_1741454 Human_miRNA_ID_2157927 RMVar_hsa_circ_94319,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086,RMVar_hsa_circ_180089,RMVar_hsa_circ_44041,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277,RMVar_hsa_circ_361949,RMVar_hsa_circ_331020,RMVar_hsa_circ_180091,RMVar_hsa_circ_180092,RMVar_hsa_circ_283420 78800 RMVar_ID_78800 Human_SNP_ID_608988895 m1A Human chr16 - 75640304 75640304 75640304 TCCGCAGTCAAGCAATTCATCAGCTGAAGGTCAATGGGGAAGACCCATACCCACACAAGTTCCAT TCCGCAGTCAAGCAATTCATCAGCTGAAGGTCCATGGGGAAGACCCATACCCACACAAGTTCCAT T G KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75640254..75640394 26863196 MeRIP-seq:(Medium) rs369759907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43690,Human_RBP_ID_1523058,Human_RBP_ID_1846885,Human_RBP_ID_4384790,Human_RBP_ID_9065665,Human_RBP_ID_17256177,Human_RBP_ID_26811558 Human_Splice_Rec_1741314,Human_Splice_Rec_1741340,Human_Splice_Rec_1741408,Human_Splice_Rec_1741434,Human_Splice_Rec_1741446,Human_Splice_Rec_1741454 Human_miRNA_ID_2157927 RMVar_hsa_circ_94319,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086,RMVar_hsa_circ_180089,RMVar_hsa_circ_44041,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277,RMVar_hsa_circ_361949,RMVar_hsa_circ_331020,RMVar_hsa_circ_180091,RMVar_hsa_circ_180092,RMVar_hsa_circ_283420 78801 RMVar_ID_78801 Human_SNP_ID_608988914 m1A Human chr16 + 75640336 75640336 75640336 TGACCTTCAGCTGATGAATTGCTTGACTGCGGATTTTGTAGTATTGCTGTTAAAAAAAAAAAAAA TGACCTTCAGCTGATGAATTGCTTGACTGCGGTTTTTGTAGTATTGCTGTTAAAAAAAAAAAAAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:75640176..75640390;chr16:75640201..75640405 26863196 MeRIP-seq:(Medium) rs765066644 Functional Loss SNV dbSNP153 33..33 33 - - - 78802 RMVar_ID_78802 Human_SNP_ID_608989358 m1A Human chr16 - 75641684 75641684 75641684 AAGAGACGCCTGAAAGCTGAGAAGAAAGTAGCAGAGAAGGAGGCCAAACAGAAAGAGCTCAGTGA AAGAGACGCCTGAAAGCTGAGAAGAAAGTAGCGGAGAAGGAGGCCAAACAGAAAGAGCTCAGTGA T C KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:75641513..75641777;chr16:75641521..75641764;chr16:75641505..75641779 26863196 MeRIP-seq:(Medium) rs1196952309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43691,Human_RBP_ID_892627,Human_RBP_ID_1523060,Human_RBP_ID_1846886,Human_RBP_ID_3499734,Human_RBP_ID_4403687,Human_RBP_ID_8439298,Human_RBP_ID_9373257,Human_RBP_ID_18411409,Human_RBP_ID_26329251 Human_Splice_Rec_1741312,Human_Splice_Rec_1741338,Human_Splice_Rec_1741370,Human_Splice_Rec_1741396,Human_Splice_Rec_1741406,Human_Splice_Rec_1741418,Human_Splice_Rec_1741432,Human_Splice_Rec_1741444 Human_miRNA_ID_3118582 RMVar_hsa_circ_94319,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086,RMVar_hsa_circ_44041,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277,RMVar_hsa_circ_180092,RMVar_hsa_circ_283420,RMVar_hsa_circ_367501,RMVar_hsa_circ_378999 78803 RMVar_ID_78803 Human_SNP_ID_608990241 m1A Human chr16 - 75644356 75644354 75644356 TGCGCAAAACCTCCTGGGCAGAGTGGGGTCACAGGGAACTGCGACTGGGTCAACTTGCTCCTTTC TGCGCAAAACCTCCTGGGCAGAGTGGGGTCAC__GGAACTGCGACTGGGTCAACTTGCTCCTTTC CCT C KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:75644351..75644480 26863196 MeRIP-seq:(Medium) rs1555513844 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_479834,Human_RBP_ID_6538748 Human_Splice_Rec_1741311,Human_Splice_Rec_1741365,Human_Splice_Rec_1741369,Human_Splice_Rec_1741443 RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277 78804 RMVar_ID_78804 Human_SNP_ID_608991390 m1A Human chr16 - 75647626 75647626 75647626 GGTCGGGCCCTCCGGGAAGATGGCGGCCGTGCAGGCGGCCGAGGTGAAAGTGGATGGCAGCGAGC GGTCGGGCCCTCCGGGAAGATGGCGGCCGTGCGGGCGGCCGAGGTGAAAGTGGATGGCAGCGAGC T C KARS1 Ensembl:ENSG00000065427 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:75647499..75647675;chr16:75647503..75647675;chr16:75647525..75647675 26863196 MeRIP-seq:(Medium) rs780519547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43692,Human_RBP_ID_760489,Human_RBP_ID_816053,Human_RBP_ID_4394009,Human_RBP_ID_22053451,Human_RBP_ID_23128610 Human_Splice_Rec_1741309,Human_Splice_Rec_1741337,Human_Splice_Rec_1741363,Human_Splice_Rec_1741367,Human_Splice_Rec_1741395,Human_Splice_Rec_1741417,Human_Splice_Rec_1741429 RMVar_hsa_circ_180090,RMVar_hsa_circ_114972 78805 RMVar_ID_78805 Human_SNP_ID_608991556 m1A Human chr16 - 75647859 75647859 75647859 CTCCGCCATGTCTGACGCCGAGCACTACTAGAAGAGCTACCCCCTCGCGAGCGCCTGGCACACAG CTCCGCCATGTCTGACGCCGAGCACTACTAGACGAGCTACCCCCTCGCGAGCGCCTGGCACACAG T G KARS1 Ensembl:ENSG00000065427 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75647818..75647904 26863196 MeRIP-seq:(Medium) rs770955473 Functional Loss SNV dbSNP153 33..33 33 - - - 78806 RMVar_ID_78806 Human_SNP_ID_608991831 m1A Human chr16 + 75648377 75648377 75648377 CCCAGCTCCGTCACCGGTAACGCCTTGTGGAAAGCGATGGAGAAGAGCTCGCTCACGCAGCACTC CCCAGCTCCGTCACCGGTAACGCCTTGTGGAAGGCGATGGAGAAGAGCTCGCTCACGCAGCACTC A G TERF2IP Ensembl:ENSG00000166848 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:75647926..75648400 32194978 MeRIP-seq:(Medium) rs531898683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5349,Human_RBP_ID_1523070,Human_RBP_ID_1846888,Human_RBP_ID_6538752,Human_RBP_ID_9285940,Human_RBP_ID_22053453 78807 RMVar_ID_78807 Human_SNP_ID_608993725 m1A Human chr16 - 75654366 75654366 75654366 CCACAACCTCCTCAAACTCCCGGGTGGCTTCCACAAGCATCTTTTTGACTGCTTCTTCATTCTCC CCACAACCTCCTCAAACTCCCGGGTGGCTTCCGCAAGCATCTTTTTGACTGCTTCTTCATTCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:75654217..75654445;chr16:75654251..75656366;chr16:75654251..75654452 26863196 MeRIP-seq:(Medium) rs139779421 Functional Loss SNV dbSNP153 33..33 33 - - - 78808 RMVar_ID_78808 Human_SNP_ID_608993726 m1A Human chr16 - 75654366 75654366 75654366 CCACAACCTCCTCAAACTCCCGGGTGGCTTCCACAAGCATCTTTTTGACTGCTTCTTCATTCTCC CCACAACCTCCTCAAACTCCCGGGTGGCTTCCCCAAGCATCTTTTTGACTGCTTCTTCATTCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:75654217..75654445;chr16:75654251..75656366;chr16:75654251..75654452 26863196 MeRIP-seq:(Medium) rs139779421 Functional Loss SNV dbSNP153 33..33 33 - - - 78809 RMVar_ID_78809 Human_SNP_ID_608994303 m1A Human chr16 - 75656221 75656221 75656221 TCACACATAGTTATATGTATTTCAAAATCAGGAGGGCTCTCATCCACCTAGACAGAATGATGAGT TCACACATAGTTATATGTATTTCAAAATCAGGCGGGCTCTCATCCACCTAGACAGAATGATGAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:75656187..75656403 26863196 MeRIP-seq:(Medium) rs1343364757 Functional Loss SNV dbSNP153 33..33 33 - - - 78810 RMVar_ID_78810 Human_SNP_ID_609183561 m1A Human chr16 - 76277400 76277400 76277400 ACACACACCTCCCTGACTCCTCACTGAAAAGCACTCAGCATCTTTCCTAACAAGCATCCACACCG ACACACACCTCCCTGACTCCTCACTGAAAAGCGCTCAGCATCTTTCCTAACAAGCATCCACACCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:76277361..76277627 26863196 MeRIP-seq:(Medium) rs1189560550 Functional Loss SNV dbSNP153 33..33 33 - - - 78811 RMVar_ID_78811 Human_SNP_ID_609183576 m1A Human chr16 + 76277434 76277432 76277434 CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGTGAGAGAGAGAGAGAAAAGAGAGAGACAGAGACGG CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGT__GAGAGAGAGAGAAAAGAGAGAGACAGAGACGG TGA T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:76277383..76277480 26863196 MeRIP-seq:(Medium) rs148229407 Functional Loss DEL dbSNP153 32..33 33 - - - 78812 RMVar_ID_78812 Human_SNP_ID_609183578 m1A Human chr16 + 76277434 76277434 76277434 CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGTGAGAGAGAGAGAGAAAAGAGAGAGACAGAGACGG CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGTGTGAGAGAGAGAGAAAAGAGAGAGACAGAGACGG A T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:76277383..76277480 26863196 MeRIP-seq:(Medium) rs1567554665 Functional Loss SNV dbSNP153 33..33 33 - - - 78813 RMVar_ID_78813 Human_SNP_ID_609473278 m1A Human chr16 - 77191237 77191237 77191237 TATACAAACACCTGTTTTAACTCCGAATCTCAATTGGCCGGATACCATTACTTCCCCGTAGCGGC TATACAAACACCTGTTTTAACTCCGAATCTCAGTTGGCCGGATACCATTACTTCCCCGTAGCGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:77191134..77191284 32194978 MeRIP-seq:(Medium) rs761224476 Functional Loss SNV dbSNP153 33..33 33 - - - 78814 RMVar_ID_78814 Human_SNP_ID_609473282 m1A Human chr16 - 77191244 77191244 77191244 ATAGAGATATACAAACACCTGTTTTAACTCCGAATCTCAATTGGCCGGATACCATTACTTCCCCG ATAGAGATATACAAACACCTGTTTTAACTCCGCATCTCAATTGGCCGGATACCATTACTTCCCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:77191195..77191436 26863196 MeRIP-seq:(Medium) rs990599585 Functional Loss SNV dbSNP153 33..33 33 - - - 78815 RMVar_ID_78815 Human_SNP_ID_609473426 m1A Human chr16 + 77191546 77191546 77191546 CGGCCCCCGGGGGCGCGGAGGACTTGGAGGACACGCAGTTCCCCAGTGAGGAAGCTAGAGAAGGT CGGCCCCCGGGGGCGCGGAGGACTTGGAGGACTCGCAGTTCCCCAGTGAGGAAGCTAGAGAAGGT A T MON1B Ensembl:ENSG00000103111 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:77191498..77192001 26863196 MeRIP-seq:(Medium) rs1204170760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888959,Human_RBP_ID_8941374,Human_RBP_ID_9373260,Human_RBP_ID_22945144 Human_Splice_Rec_1741888,Human_Splice_Rec_1741889,Human_Splice_Rec_1741894,Human_Splice_Rec_1741895,Human_Splice_Rec_1741899,Human_Splice_Rec_1741902,Human_Splice_Rec_1741903,Human_Splice_Rec_1741906,Human_Splice_Rec_1741907,Human_Splice_Rec_1741910,Human_Splice_Rec_1741911,Human_Splice_Rec_1741916,Human_Splice_Rec_1741917,Human_Splice_Rec_1741926,Human_Splice_Rec_1741927 78816 RMVar_ID_78816 Human_SNP_ID_609473442 m1A Human chr16 + 77191575 77191575 77191575 GACACGCAGTTCCCCAGTGAGGAAGCTAGAGAAGGTGGAGGGGTTCACGCGGTCCCGCCGGATCC GACACGCAGTTCCCCAGTGAGGAAGCTAGAGACGGTGGAGGGGTTCACGCGGTCCCGCCGGATCC A C MON1B Ensembl:ENSG00000103111 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:77191483..77191666 26863196 MeRIP-seq:(Medium) rs1481235905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888959,Human_RBP_ID_4385050,Human_RBP_ID_8941374,Human_RBP_ID_9373260,Human_RBP_ID_22945145 Human_Splice_Rec_1741888,Human_Splice_Rec_1741889,Human_Splice_Rec_1741894,Human_Splice_Rec_1741895,Human_Splice_Rec_1741899,Human_Splice_Rec_1741902,Human_Splice_Rec_1741903,Human_Splice_Rec_1741906,Human_Splice_Rec_1741907,Human_Splice_Rec_1741910,Human_Splice_Rec_1741911,Human_Splice_Rec_1741916,Human_Splice_Rec_1741917,Human_Splice_Rec_1741926,Human_Splice_Rec_1741927 78817 RMVar_ID_78817 Human_SNP_ID_609473461 m1A Human chr16 + 77191611 77191611 77191611 GGAGGGGTTCACGCGGTCCCGCCGGATCCCGAAGACGAGGGCCTGGAGGAAACAGGTATGACTCC GGAGGGGTTCACGCGGTCCCGCCGGATCCCGAGGACGAGGGCCTGGAGGAAACAGGTATGACTCC A G MON1B Ensembl:ENSG00000103111 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:77191483..77193437 32194978 MeRIP-seq:(Medium) rs1437461981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888959,Human_RBP_ID_8941374,Human_RBP_ID_9373260,Human_RBP_ID_22945145 Human_Splice_Rec_1741889,Human_Splice_Rec_1741895,Human_Splice_Rec_1741899,Human_Splice_Rec_1741903,Human_Splice_Rec_1741907,Human_Splice_Rec_1741911,Human_Splice_Rec_1741917,Human_Splice_Rec_1741927 78818 RMVar_ID_78818 Human_SNP_ID_609480854 m1A Human chr16 + 77212345 77212345 77212345 GGAGCGGCGGCTGCACTCGCCGCCTGAGGTCGAGGGCGCCATGGCGGTGAATGACGGGTGAGAGG GGAGCGGCGGCTGCACTCGCCGCCTGAGGTCGCGGGCGCCATGGCGGTGAATGACGGGTGAGAGG A C SYCE1L Ensembl:ENSG00000205078 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:77212327..77212461 26863410 MeRIP-seq:(Medium) rs758935078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1741958,Human_Splice_Rec_1741959 78819 RMVar_ID_78819 Human_SNP_ID_609480996 m1A Human chr16 + 77212614 77212614 77212614 CGGAGCTGGAGATATTCGGGGAGCAGGTCCGGAGCGCCCCCGAGGTCGGGGCCGGCGAGGGAGAG CGGAGCTGGAGATATTCGGGGAGCAGGTCCGGGGCGCCCCCGAGGTCGGGGCCGGCGAGGGAGAG A G SYCE1L Ensembl:ENSG00000205078 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:77212198..77212966 26863196 MeRIP-seq:(Medium) rs1342537163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1741960,Human_Splice_Rec_1741961,Human_Splice_Rec_1741963,Human_Splice_Rec_1741965 78820 RMVar_ID_78820 Human_SNP_ID_609481023 m1A Human chr16 + 77212639 77212639 77212639 GGTCCGGAGCGCCCCCGAGGTCGGGGCCGGCGAGGGAGAGGTAGGGAGCCCGAGGAAGGGAGGCG GGTCCGGAGCGCCCCCGAGGTCGGGGCCGGCGGGGGAGAGGTAGGGAGCCCGAGGAAGGGAGGCG A G SYCE1L Ensembl:ENSG00000205078 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:77212599..77212723 26863196 MeRIP-seq:(Medium) rs949648701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1741960,Human_Splice_Rec_1741961,Human_Splice_Rec_1741963,Human_Splice_Rec_1741965 78821 RMVar_ID_78821 Human_SNP_ID_609481146 m1A Human chr16 - 77212909 77212909 77212909 TCCTGCTGGCCTAGAGGGCGTCAGGGGCAGCCACCGGCGGCTCGGGATCCTCCTCGTCGCGAGCG TCCTGCTGGCCTAGAGGGCGTCAGGGGCAGCCGCCGGCGGCTCGGGATCCTCCTCGTCGCGAGCG T C AC009139.2 Ensembl:ENSG00000261063 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:77212616..77212966 26863410 MeRIP-seq:(Medium) rs1385050726 Functional Loss SNV dbSNP153 33..33 33 - - - 78822 RMVar_ID_78822 Human_SNP_ID_609780489 m1A Human chr16 + 78099825 78099822 78099826 CTACGCGGGGCTGGACGACACGGACAGTGAGGACGAGCTGCCTCCGGGCTGGGAGGAGAGAACCA CTACGCGGGGCTGGACGACACGGACAGTGA____GAGCTGCCTCCGGGCTGGGAGGAGAGAACCA AGGAC A WWOX Ensembl:ENSG00000186153 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:78099646..78099935 26863196 MeRIP-seq:(Medium) rs730880291 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_1523153,Human_RBP_ID_4394012,Human_RBP_ID_6539034,Human_RBP_ID_9373262,Human_RBP_ID_12819000,Human_RBP_ID_23700931 Human_Splice_Rec_1742139,Human_Splice_Rec_1742147,Human_Splice_Rec_1742161,Human_Splice_Rec_1742177,Human_Splice_Rec_1742185,Human_Splice_Rec_1742195,Human_Splice_Rec_1742205,Human_Splice_Rec_1742213,Human_Splice_Rec_1742221,Human_Splice_Rec_1742231,Human_Splice_Rec_1742249,Human_Splice_Rec_1742255 Clinvar_Rec_364 78823 RMVar_ID_78823 Human_SNP_ID_609811013 m1A Human chr16 + 78180737 78180737 78180737 AGCTCCATCTGAGATATGGGGTATACATGAATACTAGTGGGTAAATCCAGCTGTACACGAGAGTA AGCTCCATCTGAGATATGGGGTATACATGAATGCTAGTGGGTAAATCCAGCTGTACACGAGAGTA A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:78180689..78180817 26863196 MeRIP-seq:(Medium) rs1173740268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283334 RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_58698 78824 RMVar_ID_78824 Human_SNP_ID_610080810 m1A Human chr16 + 78783875 78783873 78783876 ATGATGGTGATATGACGCTGATGATGGTGATGACGATGATAATGGTGATGATGGTGATGACGATG ATGATGGTGATATGACGCTGATGATGGTGAT___GATGATAATGGTGATGATGGTGATGACGATG TGAC T WWOX Ensembl:ENSG00000186153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:78783836..78783936 26863196 MeRIP-seq:(Medium) rs1259915815 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_23701450 78825 RMVar_ID_78825 Human_SNP_ID_610080812 m1A Human chr16 + 78783875 78783875 78783875 ATGATGGTGATATGACGCTGATGATGGTGATGACGATGATAATGGTGATGATGGTGATGACGATG ATGATGGTGATATGACGCTGATGATGGTGATGGCGATGATAATGGTGATGATGGTGATGACGATG A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:78783836..78783936 26863196 MeRIP-seq:(Medium) rs939374086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23701450 78826 RMVar_ID_78826 Human_SNP_ID_610080813 m1A Human chr16 + 78783875 78783875 78783875 ATGATGGTGATATGACGCTGATGATGGTGATGACGATGATAATGGTGATGATGGTGATGACGATG ATGATGGTGATATGACGCTGATGATGGTGATGTCGATGATAATGGTGATGATGGTGATGACGATG A T WWOX Ensembl:ENSG00000186153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:78783836..78783936 26863196 MeRIP-seq:(Medium) rs939374086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23701450 78827 RMVar_ID_78827 Human_SNP_ID_610833408 m1A Human chr16 - 80684641 80684641 80684641 GCCGGCTCTGAGAAGGATGAGAGGCACTTTGGAAATGGGTCCCATCAGCCTGGCTTGGATTTGAA GCCGGCTCTGAGAAGGATGAGAGGCACTTTGGGAATGGGTCCCATCAGCCTGGCTTGGATTTGAA T C CDYL2 Ensembl:ENSG00000166446 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:80684591..80684685 26863196 MeRIP-seq:(Medium) rs759830866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4385462 RMVar_hsa_circ_338198,RMVar_hsa_circ_63965,RMVar_hsa_circ_180145,RMVar_hsa_circ_335027,RMVar_hsa_circ_270378 78828 RMVar_ID_78828 Human_SNP_ID_610873155 m1A Human chr16 - 80804260 80804258 80804260 ACACACACTCGCACACACACGCGCGCACACACACGCGCACACCGGACCCCGCGCGCACACGCACG ACACACACTCGCACACACACGCGCGCACACAC__GCGCACACCGGACCCCGCGCGCACACGCACG CGT C CDYL2 Ensembl:ENSG00000166446 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:80804209..80804454 26863196 MeRIP-seq:(Medium) rs1020610305 Functional Loss DEL dbSNP153 33..34 33 - - - 78829 RMVar_ID_78829 Human_SNP_ID_610915501 m1A Human chr16 + 80932044 80932044 80932044 GGCGAGTAGGAGATGAGCCAGAGGAGAGGAGGACACTGCAGACCCGGGGGGAGGGCAAGGGCGCC GGCGAGTAGGAGATGAGCCAGAGGAGAGGAGGTCACTGCAGACCCGGGGGGAGGGCAAGGGCGCC A T HSALNG0112958 RNACentral:URS0000E97E0C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:80931885..80932241 26863196 MeRIP-seq:(Medium) rs998874596 Functional Loss SNV dbSNP153 33..33 33 - - - 78830 RMVar_ID_78830 Human_SNP_ID_610937774 m1A Human chr16 + 80997443 80997443 80997443 TGGATCACAGCAGTGCAACCTGTGGATACAAGAGTGTCTTGAATATGCATAAACACATTTGTTAC TGGATCACAGCAGTGCAACCTGTGGATACAAGTGTGTCTTGAATATGCATAAACACATTTGTTAC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:80997426..80997450 26863196 MeRIP-seq:(Medium) rs746474224 Functional Loss SNV dbSNP153 33..33 33 - - - 78831 RMVar_ID_78831 Human_SNP_ID_610940839 m1A Human chr16 - 81006804 81006804 81006804 CTGGCAAGCGGTTCAGCTGTCTGCTCCCTAGCAGCCGGCCTTCGGGTCGGGCGTCTCCGCCGGCT CTGGCAAGCGGTTCAGCTGTCTGCTCCCTAGCGGCCGGCCTTCGGGTCGGGCGTCTCCGCCGGCT T C CMC2,AC009070.1 Ensembl:ENSG00000103121,Ensembl:ENSG00000286221 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:81006501..81006875 26863196 MeRIP-seq:(Medium) rs977256257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4385513,Human_RBP_ID_5113989,Human_RBP_ID_5465931,Human_RBP_ID_9325226,Human_RBP_ID_18984314,Human_RBP_ID_22053464,Human_RBP_ID_22442227 Human_Splice_Rec_1743321,Human_Splice_Rec_1743323,Human_Splice_Rec_1743329,Human_Splice_Rec_1743333,Human_Splice_Rec_1743343,Human_Splice_Rec_1743349,Human_Splice_Rec_1743353,Human_Splice_Rec_1743361,Human_Splice_Rec_1743387,Human_Splice_Rec_1743397,Human_Splice_Rec_1743403,Human_Splice_Rec_1743407,Human_Splice_Rec_1743421,Human_Splice_Rec_1743429,Human_Splice_Rec_1743441,Human_Splice_Rec_1743459,Human_Splice_Rec_1743469,Human_Splice_Rec_1743473,Human_Splice_Rec_1743479,Human_Splice_Rec_1743495,Human_Splice_Rec_1743505,Human_Splice_Rec_1743511,Human_Splice_Rec_1743519 RMVar_hsa_circ_98109,RMVar_hsa_circ_180148 78832 RMVar_ID_78832 Human_SNP_ID_610963165 m1A Human chr16 - 81076858 81076858 81076858 ATCCAGAACGCTTTTCTGAATGGGATAGTTTGAAAGAAGGGCAGGCGTCTTTGTGGCACGGTAGG ATCCAGAACGCTTTTCTGAATGGGATAGTTTGTAAGAAGGGCAGGCGTCTTTGTGGCACGGTAGG T A C16orf46,AC092718.3,AC092718.8 Ensembl:ENSG00000166455,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81076706..81076903 26863196 MeRIP-seq:(Medium) rs918418364 Functional Loss SNV dbSNP153 33..33 33 - - - 78833 RMVar_ID_78833 Human_SNP_ID_610982091 m1A Human chr16 - 81129319 81129303 81129320 GGAAGGAAGGGAAGGAAGGGAGGAAGGAAGGGAGGAAAGGAAGGAAGGAAGGAAGGAAAGAAAGA GGAAGGAAGGGAAGGAAGGGAGGAAGGAAGG_________________AAGGAAGGAAAGAAAGA TCCTTCCTTCCTTTCCTC T PKD1L2 Ensembl:ENSG00000166473 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:81129185..81129465 26863196 MeRIP-seq:(Medium) rs1396751402 Functional Loss DEL dbSNP153 32..48 33 - - - 78834 RMVar_ID_78834 Human_SNP_ID_610982093 m1A Human chr16 - 81129319 81129307 81129320 GGAAGGAAGGGAAGGAAGGGAGGAAGGAAGGGAGGAAAGGAAGGAAGGAAGGAAGGAAAGAAAGA GGAAGGAAGGGAAGGAAGGGAGGAAGGAAGG_____________AAGGAAGGAAGGAAAGAAAGA TCCTTCCTTTCCTC T PKD1L2 Ensembl:ENSG00000166473 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:81129185..81129465 26863196 MeRIP-seq:(Medium) rs1275698546 Functional Loss DEL dbSNP153 32..44 33 - - - 78835 RMVar_ID_78835 Human_SNP_ID_611098138 m1A Human chr16 - 81444950 81444950 81444950 CGGGCTCGGCGGGCGACGGGGAGGGGCGGGGGAGGCCGAGGGCGGGCCGGGGCCAGGCGCGGAGG CGGGCTCGGCGGGCGACGGGGAGGGGCGGGGGGGGCCGAGGGCGGGCCGGGGCCAGGCGCGGAGG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:81444853..81444954 26863410 MeRIP-seq:(Medium) rs1291549938 Functional Loss SNV dbSNP153 33..33 33 - - - 78836 RMVar_ID_78836 Human_SNP_ID_611098145 m1A Human chr16 - 81444961 81444960 81444961 CGGCGGCTGACCGGGCTCGGCGGGCGACGGGGAGGGGCGGGGGAGGCCGAGGGCGGGCCGGGGCC CGGCGGCTGACCGGGCTCGGCGGGCGACGGGG_GGGGCGGGGGAGGCCGAGGGCGGGCCGGGGCC CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr16:81444871..81444986;chr16:81444923..81445035 26863196,32194978 MeRIP-seq:(Medium) rs1159395806 Functional Loss DEL dbSNP153 33..33 33 - - - 78837 RMVar_ID_78837 Human_SNP_ID_611098146 m1A Human chr16 - 81444961 81444961 81444961 CGGCGGCTGACCGGGCTCGGCGGGCGACGGGGAGGGGCGGGGGAGGCCGAGGGCGGGCCGGGGCC CGGCGGCTGACCGGGCTCGGCGGGCGACGGGGGGGGGCGGGGGAGGCCGAGGGCGGGCCGGGGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr16:81444871..81444986;chr16:81444923..81445035 26863196,32194978 MeRIP-seq:(Medium) rs1013788325 Functional Loss SNV dbSNP153 33..33 33 - - - 78838 RMVar_ID_78838 Human_SNP_ID_611098172 m1A Human chr16 + 81445018 81445018 81445018 AGCCGCCGCGAGCATGCACCCGACGAGCTAGGAGGAAGCCCGGAGCCCCGCAGGAAGCGCCGAGG AGCCGCCGCGAGCATGCACCCGACGAGCTAGGCGGAAGCCCGGAGCCCCGCAGGAAGCGCCGAGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:81444973..81445101 26863196 MeRIP-seq:(Medium) rs1192004818 Functional Loss SNV dbSNP153 33..33 33 - - - 78839 RMVar_ID_78839 Human_SNP_ID_611098182 m1A Human chr16 + 81445040 81445039 81445040 ACGAGCTAGGAGGAAGCCCGGAGCCCCGCAGGAAGCGCCGAGGCCGGCCCAGCCCGCCGCACGCG ACGAGCTAGGAGGAAGCCCGGAGCCCCGCAGG_AGCGCCGAGGCCGGCCCAGCCCGCCGCACGCG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81444989..81445080 26863196 MeRIP-seq:(Medium) rs1312476107 Functional Loss DEL dbSNP153 33..33 33 - - - 78840 RMVar_ID_78840 Human_SNP_ID_611098246 m1A Human chr16 + 81445190 81445181 81445190 GCCGCCGGATCCGGGGGCCCCGCCGCCCCAGCAGCCCAGGACAGCCCCCTCTCCCCGCCCCCAGC GCCGCCGGATCCGGGGGCCCCGCC_________GCCCAGGACAGCCCCCTCTCCCCGCCCCCAGC CGCCCCAGCA C CMIP Ensembl:ENSG00000153815 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:81444877..81445400 26863196 MeRIP-seq:(Medium) rs1164287547 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_5317628 78841 RMVar_ID_78841 Human_SNP_ID_611098347 m1A Human chr16 + 81445342 81445342 81445342 GGGGGGCGACGTGTCGGCCCCCGAAGGCACGAAGATGGGCGCCGTGCCCTGCCGCCGGGCTCTTC GGGGGGCGACGTGTCGGCCCCCGAAGGCACGAGGATGGGCGCCGTGCCCTGCCGCCGGGCTCTTC A G CMIP Ensembl:ENSG00000153815 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81445291..81445401 26863196 MeRIP-seq:(Medium) rs767359726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394019,Human_RBP_ID_8812081,Human_RBP_ID_9286419,Human_RBP_ID_9374718 78842 RMVar_ID_78842 Human_SNP_ID_611098348 m1A Human chr16 + 81445342 81445342 81445342 GGGGGGCGACGTGTCGGCCCCCGAAGGCACGAAGATGGGCGCCGTGCCCTGCCGCCGGGCTCTTC GGGGGGCGACGTGTCGGCCCCCGAAGGCACGATGATGGGCGCCGTGCCCTGCCGCCGGGCTCTTC A T CMIP Ensembl:ENSG00000153815 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81445291..81445401 26863196 MeRIP-seq:(Medium) rs767359726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394019,Human_RBP_ID_8812081,Human_RBP_ID_9286419,Human_RBP_ID_9374718 78843 RMVar_ID_78843 Human_SNP_ID_611098393 m1A Human chr16 + 81445464 81445464 81445464 TCATCCGGCACCCGCGGACCTTTCTCAGCAAGATCCTCACCTCGAAATTCCTGAGGCGCTGGGAG TCATCCGGCACCCGCGGACCTTTCTCAGCAAGGTCCTCACCTCGAAATTCCTGAGGCGCTGGGAG A G CMIP Ensembl:ENSG00000153815 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:81445219..81445469 32194978 MeRIP-seq:(Medium) rs1466506674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46227,Human_RBP_ID_26810609 Human_Splice_Rec_1744215 78844 RMVar_ID_78844 Human_SNP_ID_611101493 m1A Human chr16 + 81454862 81454862 81454862 GAAGGACTTCTTTGTAGGAGACAGGCATCTGGATGGAGAGGTAGGATGGAGACTGATGGAGATGA GAAGGACTTCTTTGTAGGAGACAGGCATCTGGTTGGAGAGGTAGGATGGAGACTGATGGAGATGA A T CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81454811..81455074 26863196 MeRIP-seq:(Medium) rs1451541956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541654,Human_RBP_ID_9420689,Human_RBP_ID_12825398,Human_RBP_ID_18939450,Human_RBP_ID_23274571 78845 RMVar_ID_78845 Human_SNP_ID_611103090 m1A Human chr16 - 81459404 81459404 81459404 CCCATTCCAAATAATGGTGCCTGAGGTCACGGAGCGAGGTCACGGAGCAGGGTCACGGCACGGGG CCCATTCCAAATAATGGTGCCTGAGGTCACGGGGCGAGGTCACGGAGCAGGGTCACGGCACGGGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:81459356..81459499 26863196 MeRIP-seq:(Medium) rs1394674347 Functional Loss SNV dbSNP153 33..33 33 - - - 78846 RMVar_ID_78846 Human_SNP_ID_611110607 m1A Human chr16 + 81482403 81482403 81482403 CTGGTGGGCAGGCAATCTAAGGCCTGGAGGTGAGTGGGTGCTTGGCTTTGGAGGGGTGCTGGGCG CTGGTGGGCAGGCAATCTAAGGCCTGGAGGTGTGTGGGTGCTTGGCTTTGGAGGGGTGCTGGGCG A T CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81482392..81482488 26863196 MeRIP-seq:(Medium) rs1219088869 Functional Loss SNV dbSNP153 33..33 33 - - - 78847 RMVar_ID_78847 Human_SNP_ID_611114030 m1A Human chr16 + 81492921 81492921 81492921 AGAGAGACCCAGAAAGACAGACACACAGAGAGAAGGGAGCGGCCGAAGAGGAGGGCCCGTGAGCG AGAGAGACCCAGAAAGACAGACACACAGAGAGGAGGGAGCGGCCGAAGAGGAGGGCCCGTGAGCG A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81492692..81493038 26863196 MeRIP-seq:(Medium) rs987395444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261534,Human_RBP_ID_3502797,Human_RBP_ID_5142539,Human_RBP_ID_8184818,Human_RBP_ID_8231085,Human_RBP_ID_9419378,Human_RBP_ID_17206211,Human_RBP_ID_22415578,Human_RBP_ID_23118495,Human_RBP_ID_23274762,Human_RBP_ID_24551976,Human_RBP_ID_26779763 78848 RMVar_ID_78848 Human_SNP_ID_611115600 m1A Human chr16 - 81497806 81497806 81497806 CTTTGTAGCCCTTGAGGCTGCAGCAGCAGAGGAGGCGGCGGGGCACCTGTGTCGGCCAAGGCTCC CTTTGTAGCCCTTGAGGCTGCAGCAGCAGAGGCGGCGGCGGGGCACCTGTGTCGGCCAAGGCTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:81497800..81497901 32194978 MeRIP-seq:(Medium) rs530713087 Functional Loss SNV dbSNP153 33..33 33 - - - 78849 RMVar_ID_78849 Human_SNP_ID_611126088 m1A Human chr16 - 81529209 81529209 81529209 TCAAGATGCAGCAATAGCATTGTGACCTCCAGAAAGCTTTTCTTCATCCTCCCAACCTGCCCTAG TCAAGATGCAGCAATAGCATTGTGACCTCCAGGAAGCTTTTCTTCATCCTCCCAACCTGCCCTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81529204..81529453 26863196 MeRIP-seq:(Medium) rs190312357 Functional Loss SNV dbSNP153 33..33 33 - - - 78850 RMVar_ID_78850 Human_SNP_ID_611133292 m1A Human chr16 + 81550843 81550843 81550843 TCCTAACCCCATTCTGTGCCCTCCCCAGTTCCATCACACACACCCCAGTTCCATCACACACACCC TCCTAACCCCATTCTGTGCCCTCCCCAGTTCCGTCACACACACCCCAGTTCCATCACACACACCC A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81550832..81551164 26863196 MeRIP-seq:(Medium) rs1022700451 Functional Loss SNV dbSNP153 33..33 33 - - - 78851 RMVar_ID_78851 Human_SNP_ID_611133332 m1A Human chr16 - 81550899 81550899 81550899 ATATGTGACGGAACTGGGGTGCATGTGACGGAACTGGGGTGTGTGTGATGGAACTGGGGTGTGTG ATATGTGACGGAACTGGGGTGCATGTGACGGAGCTGGGGTGTGTGTGATGGAACTGGGGTGTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81550898..81551104 26863196 MeRIP-seq:(Medium) rs1442568575 Functional Loss SNV dbSNP153 33..33 33 - - - 78852 RMVar_ID_78852 Human_SNP_ID_611136921 m1A Human chr16 + 81561365 81561365 81561365 GACTTAGGGTGTCCTTTCCTGGGTTCAGGGACAACATTGAACAGAGCTGTGAATCAAGGGACCCA GACTTAGGGTGTCCTTTCCTGGGTTCAGGGACGACATTGAACAGAGCTGTGAATCAAGGGACCCA A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81561350..81561594 26863196 MeRIP-seq:(Medium) rs1305125132 Functional Loss SNV dbSNP153 33..33 33 - - - 78853 RMVar_ID_78853 Human_SNP_ID_611155702 m1A Human chr16 - 81615436 81615436 81615436 ACATACACCACACACACACCATACAGTTACAAATGTACACACACCACGCACACACACACACACCA ACATACACCACACACACACCATACAGTTACAACTGTACACACACCACGCACACACACACACACCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81615430..81615742 26863196 MeRIP-seq:(Medium) rs1248994752 Functional Loss SNV dbSNP153 33..33 33 - - - 78854 RMVar_ID_78854 Human_SNP_ID_611159085 m1A Human chr16 - 81626204 81626202 81626205 TCTTACACACATTCTCACGCGCACACACACTCACTCTCACACTCACACACCCCACATTCTTTTCC TCTTACACACATTCTCACGCGCACACACACT___TCTCACACTCACACACCCCACATTCTTTTCC AGTG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:81626173..81626630 26863196 MeRIP-seq:(Medium) rs1382318447 Functional Loss DEL dbSNP153 32..34 33 - - - 78855 RMVar_ID_78855 Human_SNP_ID_611159105 m1A Human chr16 - 81626220 81626218 81626220 ACACTCACACATTCACTCTTACACACATTCTCACGCGCACACACACTCACTCTCACACTCACACA ACACTCACACATTCACTCTTACACACATTCTC__GCGCACACACACTCACTCTCACACTCACACA CGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81626169..81627177 26863196 MeRIP-seq:(Medium) rs903834575 Functional Loss DEL dbSNP153 33..34 33 - - - 78856 RMVar_ID_78856 Human_SNP_ID_611159147 m1A Human chr16 + 81626270 81626267 81626271 TGAATGTGTGAGTGTGTGTGAGAGCGAGAGTGACTGAGTGTGACTGTGTGTTGTGTGGGGTGACT TGAATGTGTGAGTGTGTGTGAGAGCGAGAG____TGAGTGTGACTGTGTGTTGTGTGGGGTGACT GTGAC G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:81626246..81626407 26863196 MeRIP-seq:(Medium) rs1173588817 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5237284,Human_RBP_ID_5288768,Human_RBP_ID_5646944,Human_RBP_ID_8184829,Human_RBP_ID_17256456,Human_RBP_ID_21973156,Human_RBP_ID_23113930,Human_RBP_ID_23709070 RMVar_hsa_circ_180186,RMVar_hsa_circ_54536,RMVar_hsa_circ_315943,RMVar_hsa_circ_39184,RMVar_hsa_circ_320121 78857 RMVar_ID_78857 Human_SNP_ID_611159344 m1A Human chr16 - 81626733 81626733 81626733 ACACCACACACACACCCACACCCACTGTCATAAAATAATCTCCCCACACCACACACCCTCATACA ACACCACACACACACCCACACCCACTGTCATATAATAATCTCCCCACACCACACACCCTCATACA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:81626698..81626816 26863196 MeRIP-seq:(Medium) rs1401117282 Functional Loss SNV dbSNP153 33..33 33 - - - 78858 RMVar_ID_78858 Human_SNP_ID_611159587 m1A Human chr16 - 81627119 81627117 81627119 CATAAAATAGTTGGCCCATATGCCACACACACACCACACACACACTCTCACAGTCACCCCCACAC CATAAAATAGTTGGCCCATATGCCACACACAC__CACACACACACTCTCACAGTCACCCCCACAC GGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:81627083..81627211 26863196 MeRIP-seq:(Medium) rs1408019593 Functional Loss DEL dbSNP153 33..34 33 - - - 78859 RMVar_ID_78859 Human_SNP_ID_611159588 m1A Human chr16 - 81627119 81627119 81627119 CATAAAATAGTTGGCCCATATGCCACACACACACCACACACACACTCTCACAGTCACCCCCACAC CATAAAATAGTTGGCCCATATGCCACACACACGCCACACACACACTCTCACAGTCACCCCCACAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:81627083..81627211 26863196 MeRIP-seq:(Medium) rs1567618731 Functional Loss SNV dbSNP153 33..33 33 - - - 78860 RMVar_ID_78860 Human_SNP_ID_611167065 m1A Human chr16 + 81650366 81650366 81650366 CAATGGGTGAATGGGCAAAGAATAGTAAGACCAGGTGCTGGAAGGAGGAAAGAAAGGTGGGCAGG CAATGGGTGAATGGGCAAAGAATAGTAAGACCGGGTGCTGGAAGGAGGAAAGAAAGGTGGGCAGG A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81650359..81650522 26863196 MeRIP-seq:(Medium) rs766937525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180186,RMVar_hsa_circ_54536,RMVar_hsa_circ_315943,RMVar_hsa_circ_39184,RMVar_hsa_circ_320121 78861 RMVar_ID_78861 Human_SNP_ID_611167070 m1A Human chr16 + 81650388 81650388 81650388 TAGTAAGACCAGGTGCTGGAAGGAGGAAAGAAAGGTGGGCAGGTGGGTAGATGAAAGAACTAGAG TAGTAAGACCAGGTGCTGGAAGGAGGAAAGAAGGGTGGGCAGGTGGGTAGATGAAAGAACTAGAG A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81650327..81650556 26863196 MeRIP-seq:(Medium) rs1425178112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180186,RMVar_hsa_circ_54536,RMVar_hsa_circ_315943,RMVar_hsa_circ_39184,RMVar_hsa_circ_320121 78862 RMVar_ID_78862 Human_SNP_ID_611184734 m1A Human chr16 + 81700697 81700697 81700697 GAGAGTTCGGGCAGATGTGAGCCCTGGGGAAGAGGCAGCGGGAAGGTGGGAGCTGAGCAGGCTGT GAGAGTTCGGGCAGATGTGAGCCCTGGGGAAGGGGCAGCGGGAAGGTGGGAGCTGAGCAGGCTGT A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81700691..81700883 26863196 MeRIP-seq:(Medium) rs1339307094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2675,RMVar_hsa_circ_126580,RMVar_hsa_circ_180194,RMVar_hsa_circ_47921 78863 RMVar_ID_78863 Human_SNP_ID_611185936 m1A Human chr16 - 81704052 81704052 81704052 TGAGTGGACCACAGGTTCAGCTGCTTGAGCGAAGGCAGTTTGATGAGGTGCTCGGCGCAGGCACT TGAGTGGACCACAGGTTCAGCTGCTTGAGCGAGGGCAGTTTGATGAGGTGCTCGGCGCAGGCACT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:81704001..81704100 26863196 MeRIP-seq:(Medium) rs1475367560 Functional Loss SNV dbSNP153 33..33 33 - - - 78864 RMVar_ID_78864 Human_SNP_ID_611187466 m1A Human chr16 - 81707601 81707601 81707601 CGGTGCAGCGCAGCCCTCAGTGGTGAGGCACCAGCCCTGCTCAACCCTCCCTGCTTCTACTCCTG CGGTGCAGCGCAGCCCTCAGTGGTGAGGCACCGGCCCTGCTCAACCCTCCCTGCTTCTACTCCTG T C lnc-SDR42E1-4,lnc-SDR42E1-4:2 RNACentral:URS0000D5DF6B,RNACentral:URS0000D57621 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81707596..81707721 26863196 MeRIP-seq:(Medium) rs1228266365 Functional Loss SNV dbSNP153 33..33 33 - - - 78865 RMVar_ID_78865 Human_SNP_ID_611187928 m1A Human chr16 + 81709009 81709009 81709009 TGTAAAGGCATGAGGCCAGTTAGGAGGCAGCTACCTCTCTGTATAGTGGAGGCTTGTTAAGAAAA TGTAAAGGCATGAGGCCAGTTAGGAGGCAGCTGCCTCTCTGTATAGTGGAGGCTTGTTAAGAAAA A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81709003..81709086 26863196 MeRIP-seq:(Medium) rs1409645031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124545,RMVar_hsa_circ_180195 78866 RMVar_ID_78866 Human_SNP_ID_611188706 m1A Human chr16 + 81710898 81710898 81710898 TGCTGTCCCCTGTCCCCAACGGAGACTCTGTCACCCCTGGGCTCCCCCTGCCATCGTGTGCTTCA TGCTGTCCCCTGTCCCCAACGGAGACTCTGTCCCCCCTGGGCTCCCCCTGCCATCGTGTGCTTCA A C CMIP Ensembl:ENSG00000153815 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81710847..81710975 26863196 MeRIP-seq:(Medium) rs989086764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480283,Human_RBP_ID_8186001,Human_RBP_ID_8440075,Human_RBP_ID_17077965,Human_RBP_ID_17371535,Human_RBP_ID_18939496,Human_RBP_ID_26445431 Human_miRNA_ID_1709648,Human_miRNA_ID_2877917 RMVar_hsa_circ_124545,RMVar_hsa_circ_180195 78867 RMVar_ID_78867 Human_SNP_ID_611191817 m1A Human chr16 - 81719349 81719349 81719349 GACGAGACGAGACGAGACGAGACGAGACTGGAACTGCAAAGATTGCAGCTGTGATAAAGGATCTC GACGAGACGAGACGAGACGAGACGAGACTGGAGCTGCAAAGATTGCAGCTGTGATAAAGGATCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:81719187..81719428 26863196 MeRIP-seq:(Medium) rs989713066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5572081 78868 RMVar_ID_78868 Human_SNP_ID_611214630 m1A Human chr16 - 81779357 81779339 81779357 CCCGGGTTTGGGCTCCGGGGTCCCGCGCGCGCAGCCCGCGTCCCGACTCGGGTCACTCAGCGCCG CCCGGGTTTGGGCTCCGGGGTCCCGCGCGCGC__________________GGTCACTCAGCGCCG CCGAGTCGGGACGCGGGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:81779309..81779390;chr16:81779310..81779389;chr16:81779308..81779422 26863196 MeRIP-seq:(Medium) rs1404853259 Functional Loss DEL dbSNP153 33..50 33 - - - 78869 RMVar_ID_78869 Human_SNP_ID_611214649 m1A Human chr16 - 81779357 81779357 81779357 CCCGGGTTTGGGCTCCGGGGTCCCGCGCGCGCAGCCCGCGTCCCGACTCGGGTCACTCAGCGCCG CCCGGGTTTGGGCTCCGGGGTCCCGCGCGCGCCGCCCGCGTCCCGACTCGGGTCACTCAGCGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:81779309..81779390;chr16:81779310..81779389;chr16:81779308..81779422 26863196 MeRIP-seq:(Medium) rs540965735 Functional Loss SNV dbSNP153 33..33 33 - - - 78870 RMVar_ID_78870 Human_SNP_ID_611239708 m1A Human chr16 + 81842842 81842841 81842842 TGAGAGGAAGCTATGAGACGTACGGAGGGGCCAAAAGTCCGCAAGGCTGTGCCAGAAGGTGATGG TGAGAGGAAGCTATGAGACGTACGGAGGGGCC_AAAGTCCGCAAGGCTGTGCCAGAAGGTGATGG CA C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81842792..81842886 26863196 MeRIP-seq:(Medium) rs1407611072 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1744661 RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_40569,RMVar_hsa_circ_180198 78871 RMVar_ID_78871 Human_SNP_ID_611239709 m1A Human chr16 + 81842842 81842842 81842842 TGAGAGGAAGCTATGAGACGTACGGAGGGGCCAAAAGTCCGCAAGGCTGTGCCAGAAGGTGATGG TGAGAGGAAGCTATGAGACGTACGGAGGGGCCCAAAGTCCGCAAGGCTGTGCCAGAAGGTGATGG A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:81842792..81842886 26863196 MeRIP-seq:(Medium) rs59929735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1744661 RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_40569,RMVar_hsa_circ_180198 78872 RMVar_ID_78872 Human_SNP_ID_611350277 m1A Human chr16 - 82148329 82148329 82148329 CAAGCCAATTCGTACATACAATTTGGAATCAAATGTCATAAGAATTTATTATATAAATTTATCAA CAAGCCAATTCGTACATACAATTTGGAATCAATTGTCATAAGAATTTATTATATAAATTTATCAA T A MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1056675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2486631,Human_RBP_ID_22942845,Human_RBP_ID_26443825 Human_miRNA_ID_1411505,Human_miRNA_ID_2527332,Human_miRNA_ID_2530510 GWAS_ID_9498,GWAS_ID_9499,GWAS_ID_9500,GWAS_ID_9501,GWAS_ID_9502,GWAS_ID_9503 RMVar_hsa_circ_77577,RMVar_hsa_circ_126209,RMVar_hsa_circ_360044,RMVar_hsa_circ_180232,RMVar_hsa_circ_180233 78873 RMVar_ID_78873 Human_SNP_ID_611350278 m1A Human chr16 - 82148329 82148329 82148329 CAAGCCAATTCGTACATACAATTTGGAATCAAATGTCATAAGAATTTATTATATAAATTTATCAA CAAGCCAATTCGTACATACAATTTGGAATCAAGTGTCATAAGAATTTATTATATAAATTTATCAA T C MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1056675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2486631,Human_RBP_ID_22942845,Human_RBP_ID_26443825 Human_miRNA_ID_1411505,Human_miRNA_ID_2527332,Human_miRNA_ID_2530510 GWAS_ID_9498,GWAS_ID_9499,GWAS_ID_9500,GWAS_ID_9501,GWAS_ID_9502,GWAS_ID_9503 RMVar_hsa_circ_77577,RMVar_hsa_circ_126209,RMVar_hsa_circ_360044,RMVar_hsa_circ_180232,RMVar_hsa_circ_180233 78874 RMVar_ID_78874 Human_SNP_ID_611350439 m1A Human chr16 - 82148798 82148798 82148798 GTTTGCCAGAAAGAGAGACCATGCCAATTATGAAGAAGATGAAAATGGAGACATAACACCAATTA GTTTGCCAGAAAGAGAGACCATGCCAATTATGGAGAAGATGAAAATGGAGACATAACACCAATTA T C MPHOSPH6 Ensembl:ENSG00000135698 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:82148747..82149343 26863196 MeRIP-seq:(Medium) rs1271187570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_198667,Human_RBP_ID_480336,Human_RBP_ID_1523358,Human_RBP_ID_1847220,Human_RBP_ID_6541953,Human_RBP_ID_8440119,Human_RBP_ID_9373271,Human_RBP_ID_23702552,Human_RBP_ID_24544723,Human_RBP_ID_25233570,Human_RBP_ID_26329258,Human_RBP_ID_26950048 Human_Splice_Rec_1744788,Human_Splice_Rec_1744798,Human_Splice_Rec_1744806 RMVar_hsa_circ_77577,RMVar_hsa_circ_126209,RMVar_hsa_circ_360044,RMVar_hsa_circ_180232,RMVar_hsa_circ_180233 78875 RMVar_ID_78875 Human_SNP_ID_611355751 m1A Human chr16 - 82164196 82164196 82164196 AAGTTTCTGACATTGATTTTGTTTGTTTTCACAGTTTATGCAAAGGGGACTGGACTCAGAAACCA AAGTTTCTGACATTGATTTTGTTTGTTTTCACGGTTTATGCAAAGGGGACTGGACTCAGAAACCA T C MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:82164165..82164267 26863410 MeRIP-seq:(Medium) rs781605891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892671,Human_RBP_ID_22055231,Human_RBP_ID_22652387,Human_RBP_ID_24544549 Human_Splice_Rec_1744801 RMVar_hsa_circ_126209,RMVar_hsa_circ_21575,RMVar_hsa_circ_180233 78876 RMVar_ID_78876 Human_SNP_ID_611358113 m1A Human chr16 + 82170075 82170075 82170075 CCGCCCGCCGCCTCGGCCCCGGCCAGGTTGGAAGGACCGGGTGCCCCTACCGCCCGGAGTGGCGC CCGCCCGCCGCCTCGGCCCCGGCCAGGTTGGAGGGACCGGGTGCCCCTACCGCCCGGAGTGGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:82170073..82170180 26863196 MeRIP-seq:(Medium) rs1411496540 Functional Loss SNV dbSNP153 33..33 33 - - - 78877 RMVar_ID_78877 Human_SNP_ID_611358149 m1A Human chr16 - 82170102 82170102 82170102 GCGCATGAAGGTGCGGGGACGCTGAGAGCGCCACTCCGGGCGGTAGGGGCACCCGGTCCTTCCAA GCGCATGAAGGTGCGGGGACGCTGAGAGCGCCGCTCCGGGCGGTAGGGGCACCCGGTCCTTCCAA T C MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:82170101..82170203 26863410 MeRIP-seq:(Medium) rs762414929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19072180 Human_Splice_Rec_1744799 RMVar_hsa_circ_126209,RMVar_hsa_circ_180233 78878 RMVar_ID_78878 Human_SNP_ID_611358150 m1A Human chr16 - 82170102 82170102 82170102 GCGCATGAAGGTGCGGGGACGCTGAGAGCGCCACTCCGGGCGGTAGGGGCACCCGGTCCTTCCAA GCGCATGAAGGTGCGGGGACGCTGAGAGCGCCCCTCCGGGCGGTAGGGGCACCCGGTCCTTCCAA T G MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:82170101..82170203 26863410 MeRIP-seq:(Medium) rs762414929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19072180 Human_Splice_Rec_1744799 RMVar_hsa_circ_126209,RMVar_hsa_circ_180233 78879 RMVar_ID_78879 Human_SNP_ID_611526220 m1A Human chr16 - 82649320 82649316 82649320 TATCAATGTATCCATCCATCATCCATCCATCCATCCTCCATCTATGCATTCATCCTTCCATCCAT TATCAATGTATCCATCCATCATCCATCCATCC____TCCATCTATGCATTCATCCTTCCATCCAT AGGAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:82649293..82649390 26863196 MeRIP-seq:(Medium) rs1360753947 Functional Loss DEL dbSNP153 33..36 33 - - - 78880 RMVar_ID_78880 Human_SNP_ID_611588565 m1A Human chr16 + 82812463 82812463 82812463 AGCCTAAAAATGAGACTTTGGAGGGAGCAGCCACAAAGATAGGAGAAAAGCCAGGTGAGGTGGTG AGCCTAAAAATGAGACTTTGGAGGGAGCAGCCTCAAAGATAGGAGAAAAGCCAGGTGAGGTGGTG A T AC099506.1,CDH13 Ensembl:ENSG00000260862,Ensembl:ENSG00000140945 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:82812433..82812589 26863196 MeRIP-seq:(Medium) rs991016815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96185,RMVar_hsa_circ_180235 78881 RMVar_ID_78881 Human_SNP_ID_611659190 m1A Human chr16 - 82996970 82996970 82996970 TCATCATCATCACCACCATCACCATCATCATTACCACCACCACCACCATCATCAACAACACCATC TCATCATCATCACCACCATCACCATCATCATTGCCACCACCACCACCATCATCAACAACACCATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:82996949..82997197 26863196 MeRIP-seq:(Medium) rs960450251 Functional Loss SNV dbSNP153 33..33 33 - - - 78882 RMVar_ID_78882 Human_SNP_ID_611659205 m1A Human chr16 + 82996996 82996996 82996996 TGGTGGTAATGATGATGGTGATGGTGGTGATGATGATGATAGTGATGGTGATGGTGATGATGGTG TGGTGGTAATGATGATGGTGATGGTGGTGATGGTGATGATAGTGATGGTGATGGTGATGATGGTG A G CDH13 Ensembl:ENSG00000140945 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:82996987..82997186 26863196 MeRIP-seq:(Medium) rs1385358179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96185,RMVar_hsa_circ_180235,RMVar_hsa_circ_30492,RMVar_hsa_circ_109852,RMVar_hsa_circ_298921,RMVar_hsa_circ_293822,RMVar_hsa_circ_43281,RMVar_hsa_circ_180237 78883 RMVar_ID_78883 Human_SNP_ID_611659220 m1A Human chr16 - 82997012 82997008 82997013 TCATCATCACCACCATCACCATCATCACCATCACCATCACTATCATCATCATCACCACCATCACC TCATCATCACCACCATCACCATCATCACCAT_____TCACTATCATCATCATCACCACCATCACC ATGGTG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:82996950..82997077 26863196 MeRIP-seq:(Medium) rs1567728457 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_2486677 78884 RMVar_ID_78884 Human_SNP_ID_611877338 m1A Human chr16 - 83559508 83559508 83559508 GGAGTGCAATGACATGATCTTGGCTCACCACAACCTCTGTCTCCCAGGTTCAAGTGATTCTCCCA GGAGTGCAATGACATGATCTTGGCTCACCACATCCTCTGTCTCCCAGGTTCAAGTGATTCTCCCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:83559502..83559608 26863196 MeRIP-seq:(Medium) rs1567763531 Functional Loss SNV dbSNP153 33..33 33 - - - 78885 RMVar_ID_78885 Human_SNP_ID_611961522 m1A Human chr16 + 83808075 83808075 83808075 CTGAGACATCACCGCCAAGCTGGGCATCGGGGAGATGGCCGAGACTGACCCCAAGACCGTGCAGG CTGAGACATCACCGCCAAGCTGGGCATCGGGGTGATGGCCGAGACTGACCCCAAGACCGTGCAGG A T HSBP1 Ensembl:ENSG00000230989 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:83808001..83808241 26863196 MeRIP-seq:(Medium) rs1254261537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480392,Human_RBP_ID_762310,Human_RBP_ID_1523395,Human_RBP_ID_4386079,Human_RBP_ID_5141969,Human_RBP_ID_5316716,Human_RBP_ID_6542241,Human_RBP_ID_8440164,Human_RBP_ID_9066090,Human_RBP_ID_9326106,Human_RBP_ID_12827312,Human_RBP_ID_17653579,Human_RBP_ID_18685400,Human_RBP_ID_22441136,Human_RBP_ID_23209714,Human_RBP_ID_23702679,Human_RBP_ID_26950103,Human_RBP_ID_27446035 Human_Splice_Rec_1745105,Human_Splice_Rec_1745109 RMVar_hsa_circ_180248,RMVar_hsa_circ_101469 78886 RMVar_ID_78886 Human_SNP_ID_611961534 m1A Human chr16 + 83808095 83808095 83808095 TGGGCATCGGGGAGATGGCCGAGACTGACCCCAAGACCGTGCAGGACCTCACCTCGGTGGTAAGG TGGGCATCGGGGAGATGGCCGAGACTGACCCCGAGACCGTGCAGGACCTCACCTCGGTGGTAAGG A G HSBP1 Ensembl:ENSG00000230989 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:83808026..83808100 32194978 MeRIP-seq:(Medium) rs1440644446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480393,Human_RBP_ID_762310,Human_RBP_ID_817722,Human_RBP_ID_894802,Human_RBP_ID_1523395,Human_RBP_ID_4386079,Human_RBP_ID_5141969,Human_RBP_ID_5316716,Human_RBP_ID_6542241,Human_RBP_ID_8440164,Human_RBP_ID_9326106,Human_RBP_ID_12827312,Human_RBP_ID_18685400,Human_RBP_ID_22441136,Human_RBP_ID_23209714,Human_RBP_ID_23702679,Human_RBP_ID_27446035 Human_Splice_Rec_1745105,Human_Splice_Rec_1745109 Human_miRNA_ID_2007530 RMVar_hsa_circ_180248,RMVar_hsa_circ_101469 78887 RMVar_ID_78887 Human_SNP_ID_611962058 m1A Human chr16 + 83809308 83809305 83809308 TTGGCACGCGTTGTCTTTAACTTCAGCACTTGATGATATGAGTAGTCGCATTGATGATCTGGAAA TTGGCACGCGTTGTCTTTAACTTCAGCACT___TGATATGAGTAGTCGCATTGATGATCTGGAAA TTGA T HSBP1 Ensembl:ENSG00000230989 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83809301..83811609 32194978 MeRIP-seq:(Medium) rs1480308947 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1523399,Human_RBP_ID_5113993,Human_RBP_ID_9373275,Human_RBP_ID_17653104,Human_RBP_ID_17883581,Human_RBP_ID_22759909,Human_RBP_ID_23702681 RMVar_hsa_circ_180249,RMVar_hsa_circ_105491,RMVar_hsa_circ_180248,RMVar_hsa_circ_101469,RMVar_hsa_circ_371076,RMVar_hsa_circ_180250,RMVar_hsa_circ_93079,RMVar_hsa_circ_180251 78888 RMVar_ID_78888 Human_SNP_ID_611963202 m1A Human chr16 + 83812775 83812773 83812775 TTGTGATGCAGGCTGGAGCCCCCGAATGCCCCACACACACTGCAGCATTGACCAGACCATCCGAA TTGTGATGCAGGCTGGAGCCCCCGAATGCCC__CACACACTGCAGCATTGACCAGACCATCCGAA CCA C HSBP1 Ensembl:ENSG00000230989 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83812605..83812975 32194978 MeRIP-seq:(Medium) rs1206650366 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_480446,Human_RBP_ID_1366666,Human_RBP_ID_1523415,Human_RBP_ID_6542286,Human_RBP_ID_8186003,Human_RBP_ID_26446407 Human_miRNA_ID_1418715,Human_miRNA_ID_2076434 RMVar_hsa_circ_105491,RMVar_hsa_circ_180248,RMVar_hsa_circ_101469,RMVar_hsa_circ_180250,RMVar_hsa_circ_76856,RMVar_hsa_circ_93079,RMVar_hsa_circ_180251,RMVar_hsa_circ_180252,RMVar_hsa_circ_180255 78889 RMVar_ID_78889 Human_SNP_ID_611963203 m1A Human chr16 + 83812775 83812775 83812775 TTGTGATGCAGGCTGGAGCCCCCGAATGCCCCACACACACTGCAGCATTGACCAGACCATCCGAA TTGTGATGCAGGCTGGAGCCCCCGAATGCCCCCCACACACTGCAGCATTGACCAGACCATCCGAA A C HSBP1 Ensembl:ENSG00000230989 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83812605..83812975 32194978 MeRIP-seq:(Medium) rs774625535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480446,Human_RBP_ID_1366666,Human_RBP_ID_1523415,Human_RBP_ID_6542286,Human_RBP_ID_8186003,Human_RBP_ID_26446407 Human_miRNA_ID_1418715,Human_miRNA_ID_2076434 RMVar_hsa_circ_105491,RMVar_hsa_circ_180248,RMVar_hsa_circ_101469,RMVar_hsa_circ_180250,RMVar_hsa_circ_76856,RMVar_hsa_circ_93079,RMVar_hsa_circ_180251,RMVar_hsa_circ_180252,RMVar_hsa_circ_180255 78890 RMVar_ID_78890 Human_SNP_ID_611963204 m1A Human chr16 + 83812775 83812775 83812775 TTGTGATGCAGGCTGGAGCCCCCGAATGCCCCACACACACTGCAGCATTGACCAGACCATCCGAA TTGTGATGCAGGCTGGAGCCCCCGAATGCCCCTCACACACTGCAGCATTGACCAGACCATCCGAA A T HSBP1 Ensembl:ENSG00000230989 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83812605..83812975 32194978 MeRIP-seq:(Medium) rs774625535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480446,Human_RBP_ID_1366666,Human_RBP_ID_1523415,Human_RBP_ID_6542286,Human_RBP_ID_8186003,Human_RBP_ID_26446407 Human_miRNA_ID_1418715,Human_miRNA_ID_2076434 RMVar_hsa_circ_105491,RMVar_hsa_circ_180248,RMVar_hsa_circ_101469,RMVar_hsa_circ_180250,RMVar_hsa_circ_76856,RMVar_hsa_circ_93079,RMVar_hsa_circ_180251,RMVar_hsa_circ_180252,RMVar_hsa_circ_180255 78891 RMVar_ID_78891 Human_SNP_ID_611963209 m1A Human chr16 - 83812790 83812790 83812790 ACCAGGGACGCAGGTTTCGGATGGTCTGGTCAATGCTGCAGTGTGTGTGGGGCATTCGGGGGCTC ACCAGGGACGCAGGTTTCGGATGGTCTGGTCAGTGCTGCAGTGTGTGTGGGGCATTCGGGGGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:83812741..83812899 26863196 MeRIP-seq:(Medium) rs1348543241 Functional Loss SNV dbSNP153 33..33 33 - - - 78892 RMVar_ID_78892 Human_SNP_ID_612004129 m1A Human chr16 - 83921043 83921043 83921043 TTCCTTCCACCCACCCAGCCATCTATTCATATACCCATCTTCCTTCTATCCACCCTCCACCATCC TTCCTTCCACCCACCCAGCCATCTATTCATATCCCCATCTTCCTTCTATCCACCCTCCACCATCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:83920995..83921199;chr16:83920976..83921164 26863196 MeRIP-seq:(Medium) rs1220644090 Functional Loss SNV dbSNP153 33..33 33 - - - 78893 RMVar_ID_78893 Human_SNP_ID_612017285 m1A Human chr16 + 83953329 83953329 83953329 GATCCGTGTTCCCCTGACCCTCCTAGTGCACAACTTGGCCGGGCTCACTGGGCTCCTGCACCACT GATCCGTGTTCCCCTGACCCTCCTAGTGCACAGCTTGGCCGGGCTCACTGGGCTCCTGCACCACT A G OSGIN1 Ensembl:ENSG00000140961 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:83953281..83953416 26863196 MeRIP-seq:(Medium) rs775109900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418799,Human_RBP_ID_27246561,Human_RBP_ID_27446058 Human_Splice_Rec_1745160,Human_Splice_Rec_1745161,Human_Splice_Rec_1745187,Human_Splice_Rec_1745195,Human_Splice_Rec_1745197 RMVar_hsa_circ_126880,RMVar_hsa_circ_180261 78894 RMVar_ID_78894 Human_SNP_ID_612018862 m1A Human chr16 + 83957691 83957691 83957691 CCCCCCACCAGCCATGAGCTCCTCCAGAAAGGACCACCTCGGCGCCAGCAGCTCAGAGCCCCTCC CCCCCCACCAGCCATGAGCTCCTCCAGAAAGGCCCACCTCGGCGCCAGCAGCTCAGAGCCCCTCC A C OSGIN1 Ensembl:ENSG00000140961 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:83957583..83957724 26863196 MeRIP-seq:(Medium) rs1369980477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1745162,Human_Splice_Rec_1745166,Human_Splice_Rec_1745167,Human_Splice_Rec_1745178,Human_Splice_Rec_1745179,Human_Splice_Rec_1745188,Human_Splice_Rec_1745189,Human_Splice_Rec_1745198,Human_Splice_Rec_1745199,Human_Splice_Rec_1745208,Human_Splice_Rec_1745209 RMVar_hsa_circ_63630,RMVar_hsa_circ_126880,RMVar_hsa_circ_180261 78895 RMVar_ID_78895 Human_SNP_ID_612019482 m1A Human chr16 + 83959314 83959314 83959314 CCTGTCCTACCTGCTCTCCGGCTACACACCCTACACGAAGCCAGATGCCATCCACCCACACCCCC CCTGTCCTACCTGCTCTCCGGCTACACACCCTTCACGAAGCCAGATGCCATCCACCCACACCCCC A T OSGIN1 Ensembl:ENSG00000140961 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:83959209..83959327 26863196 MeRIP-seq:(Medium) rs769740540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9374726,Human_RBP_ID_27446059 Human_Splice_Rec_1745168,Human_Splice_Rec_1745169,Human_Splice_Rec_1745180,Human_Splice_Rec_1745181,Human_Splice_Rec_1745190,Human_Splice_Rec_1745191,Human_Splice_Rec_1745200,Human_Splice_Rec_1745201,Human_Splice_Rec_1745210,Human_Splice_Rec_1745211 RMVar_hsa_circ_63630,RMVar_hsa_circ_126880,RMVar_hsa_circ_180261,RMVar_hsa_circ_180262,RMVar_hsa_circ_111798 78896 RMVar_ID_78896 Human_SNP_ID_612023262 m1A Human chr16 + 83968541 83968539 83968541 CCCGCGGTGTCCGCGGCCGCGGGGGCAGCGGGAGAGAGGGCGGGGCGGCGCGGGCAGCGCGGGGA CCCGCGGTGTCCGCGGCCGCGGGGGCAGCGG__GAGAGGGCGGGGCGGCGCGGGCAGCGCGGGGA GGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:83968387..83968574 26863196 MeRIP-seq:(Medium) rs922646053 Functional Loss DEL dbSNP153 32..33 33 - - - 78897 RMVar_ID_78897 Human_SNP_ID_612041075 m1A Human chr16 + 84001937 84001937 84001937 TCTTGGTGCCAGGTAGGGGGCAAAGGCCTGGAACTGCAGTGGCCACCTGACTGGAGAGAAGGGCA TCTTGGTGCCAGGTAGGGGGCAAAGGCCTGGACCTGCAGTGGCCACCTGACTGGAGAGAAGGGCA A C NECAB2 Ensembl:ENSG00000103154 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84001922..84002022 32194978 MeRIP-seq:(Medium) rs2271301 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_9504,GWAS_ID_9505 78898 RMVar_ID_78898 Human_SNP_ID_612068188 m1A Human chr16 - 84054421 84054421 84054421 TGTGACCGGCAGCCTGGCTGACCGTGAGGGCCAGAGAGAGCCTTCACGGACGGCGCTGGTGGGTG TGTGACCGGCAGCCTGGCTGACCGTGAGGGCCGGAGAGAGCCTTCACGGACGGCGCTGGTGGGTG T C MBTPS1 Ensembl:ENSG00000140943 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84054376..84054425 32194978 MeRIP-seq:(Medium) rs2280026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8440198,Human_RBP_ID_18469929,Human_RBP_ID_18685426,Human_RBP_ID_27446080 78899 RMVar_ID_78899 Human_SNP_ID_612070554 m1A Human chr16 + 84060800 84060800 84060800 CCATACGATGTGTACTGGAGGAGGGCATCCAGAAGCCAAAAGCAGTCTGCGAAGTCAACAAGCCT CCATACGATGTGTACTGGAGGAGGGCATCCAGCAGCCAAAAGCAGTCTGCGAAGTCAACAAGCCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84060751..84060871 32194978 MeRIP-seq:(Medium) rs773538029 Functional Loss SNV dbSNP153 33..33 33 - - - 78900 RMVar_ID_78900 Human_SNP_ID_612070555 m1A Human chr16 + 84060800 84060800 84060800 CCATACGATGTGTACTGGAGGAGGGCATCCAGAAGCCAAAAGCAGTCTGCGAAGTCAACAAGCCT CCATACGATGTGTACTGGAGGAGGGCATCCAGGAGCCAAAAGCAGTCTGCGAAGTCAACAAGCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84060751..84060871 32194978 MeRIP-seq:(Medium) rs773538029 Functional Loss SNV dbSNP153 33..33 33 - - - 78901 RMVar_ID_78901 Human_SNP_ID_612090197 m1A Human chr16 + 84116771 84116769 84116771 GCCGCCGGGAGCTCAGGGCCGGCGGGCCCGGGATAACGGCGCCTCCGCGGCGAACACGCCTGGGC GCCGCCGGGAGCTCAGGGCCGGCGGGCCCGG__TAACGGCGCCTCCGCGGCGAACACGCCTGGGC GGA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84116755..84116856 32194978 MeRIP-seq:(Medium) rs1034854987 Functional Loss DEL dbSNP153 32..33 33 - - - 78902 RMVar_ID_78902 Human_SNP_ID_612090200 m1A Human chr16 + 84116771 84116771 84116771 GCCGCCGGGAGCTCAGGGCCGGCGGGCCCGGGATAACGGCGCCTCCGCGGCGAACACGCCTGGGC GCCGCCGGGAGCTCAGGGCCGGCGGGCCCGGGTTAACGGCGCCTCCGCGGCGAACACGCCTGGGC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84116755..84116856 32194978 MeRIP-seq:(Medium) rs933405378 Functional Loss SNV dbSNP153 33..33 33 - - - 78903 RMVar_ID_78903 Human_SNP_ID_612093068 m1A Human chr16 - 84125013 84125013 84125013 GTGATTGGTGGGTATTTGTTTGATTGGTGGGTATTGTGATTGGTGGGTATTTGTTTGATTGGTGT GTGATTGGTGGGTATTTGTTTGATTGGTGGGTGTTGTGATTGGTGGGTATTTGTTTGATTGGTGT T C HSDL1 Ensembl:ENSG00000103160 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84124964..84125040 26863196 MeRIP-seq:(Medium) rs1222446253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27838282 78904 RMVar_ID_78904 Human_SNP_ID_612097063 m1A Human chr16 - 84135593 84135593 84135593 CTTGTTGGTTTTATTCACAGATTGGCCTTAAGAGAAGGACGGAGCCACATACTGCTGACGGCCCA CTTGTTGGTTTTATTCACAGATTGGCCTTAAGGGAAGGACGGAGCCACATACTGCTGACGGCCCA T C HSDL1 Ensembl:ENSG00000103160 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:84135526..84139270;chr16:84131287..84139270 26863196 MeRIP-seq:(Medium) rs1213978785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816931,Human_RBP_ID_4386437,Human_RBP_ID_5236660,Human_RBP_ID_5317646,Human_RBP_ID_9325239,Human_RBP_ID_9373286,Human_RBP_ID_12828686,Human_RBP_ID_18987026 Human_Splice_Rec_1745456,Human_Splice_Rec_1745457,Human_Splice_Rec_1745468,Human_Splice_Rec_1745469,Human_Splice_Rec_1745480,Human_Splice_Rec_1745481,Human_Splice_Rec_1745486,Human_Splice_Rec_1745487,Human_Splice_Rec_1745492,Human_Splice_Rec_1745493,Human_Splice_Rec_1745498,Human_Splice_Rec_1745499 RMVar_hsa_circ_307631,RMVar_hsa_circ_180292 78905 RMVar_ID_78905 Human_SNP_ID_612098485 m1A Human chr16 - 84139995 84139993 84139996 TTGGTGCTTGTTAGGAAGTGATTGAACGGAGGAGAAGACATGGGACTTGAAACGTCAGGAAGAAC TTGGTGCTTGTTAGGAAGTGATTGAACGGAG___AAGACATGGGACTTGAAACGTCAGGAAGAAC TCTC T HSDL1 Ensembl:ENSG00000103160 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:84139993..84140096 26863196 MeRIP-seq:(Medium) rs1385031940 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12828705 78906 RMVar_ID_78906 Human_SNP_ID_612100419 m1A Human chr16 + 84145118 84145118 84145118 GCCGGCAAAGTCTTCCAAACCGGTCCCGCCAGACCCGCGCGGCCGCCGCCCCCGTCTCGGCCGCC GCCGGCAAAGTCTTCCAAACCGGTCCCGCCAGGCCCGCGCGGCCGCCGCCCCCGTCTCGGCCGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:84145019..84145137 26863196 MeRIP-seq:(Medium) rs1325606350 Functional Loss SNV dbSNP153 33..33 33 - - - 78907 RMVar_ID_78907 Human_SNP_ID_612112715 m1A Human chr16 + 84178494 84178494 84178494 GATTGACAAAGCAACCCACAACAGCAGCTGCCAACGGCCGCTGTGCCCACCTCATCAGCAGCTCT GATTGACAAAGCAACCCACAACAGCAGCTGCCGACGGCCGCTGTGCCCACCTCATCAGCAGCTCT A G DNAAF1 Ensembl:ENSG00000154099 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84178443..84178544 32194978 MeRIP-seq:(Medium) rs930924740 Functional Loss SNV dbSNP153 33..33 33 - - - 78908 RMVar_ID_78908 Human_SNP_ID_612112954 m1A Human chr16 + 84179030 84179015 84179030 GTGCTGCTGGGAGCGAGTGGCCCGGACGCTGGAGGCCTGGGAGTGGGGAGGTGTGGTGGCACAGC GTGCTGCTGGGAGCGAGT_______________GGCCTGGGAGTGGGGAGGTGTGGTGGCACAGC TGGCCCGGACGCTGGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84178979..84179057 26863196 MeRIP-seq:(Medium) rs1256754846 Functional Loss DEL dbSNP153 19..33 33 - - - 78909 RMVar_ID_78909 Human_SNP_ID_612113465 m1A Human chr16 - 84179735 84179735 84179735 TCTACCAGCAGCTCCGCCCCCAGGTGGACTCCAGCCTCCGCAGAGATGCTGGGCCTCCTGGCGAC TCTACCAGCAGCTCCGCCCCCAGGTGGACTCCGGCCTCCGCAGAGATGCTGGGCCTCCTGGCGAC T C TAF1C Ensembl:ENSG00000103168 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84179140..84180032 32194978 MeRIP-seq:(Medium) rs369203744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234696,Human_RBP_ID_5113661,Human_RBP_ID_5524692,Human_RBP_ID_18162138 78910 RMVar_ID_78910 Human_SNP_ID_612114396 m1A Human chr16 + 84181414 84181414 84181414 GTGCGCAGTGAAGTCTGCCCAACGCCACGAAGAGGAGTCCCGGAACACGAGGGTCTCAGGGTCCC GTGCGCAGTGAAGTCTGCCCAACGCCACGAAGGGGAGTCCCGGAACACGAGGGTCTCAGGGTCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84181365..84181466 32194978 MeRIP-seq:(Medium) rs1296342694 Functional Loss SNV dbSNP153 33..33 33 - - - 78911 RMVar_ID_78911 Human_SNP_ID_612114652 m1A Human chr16 + 84181846 84181846 84181846 ACCAAACTTCCACACGGCACAGTGGTAGTCAGAGCGGACGGCCAGCAGAGCTGAGGAGGGATGGA ACCAAACTTCCACACGGCACAGTGGTAGTCAGCGCGGACGGCCAGCAGAGCTGAGGAGGGATGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84181796..84181896 32194978 MeRIP-seq:(Medium) rs1465289355 Functional Loss SNV dbSNP153 33..33 33 - - - 78912 RMVar_ID_78912 Human_SNP_ID_612157182 m1A Human chr16 + 84295005 84295005 84295005 TGCCTTTAACCGGCGTGGGGCCGGGCAGCTGCAGGAGGCAGATCATCCGGGCTCTGTGCCTCTTG TGCCTTTAACCGGCGTGGGGCCGGGCAGCTGCGGGAGGCAGATCATCCGGGCTCTGTGCCTCTTG A G WFDC1 Ensembl:ENSG00000103175 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:84294695..84295038 26863196 MeRIP-seq:(Medium) rs11547593 Functional Loss SNV dbSNP153 33..33 33 - - - 78913 RMVar_ID_78913 Human_SNP_ID_612162484 m1A Human chr16 + 84309234 84309234 84309234 CATGTAAGGACAAGGAGGGTCGGGGCGATGAGATGAGGCCAATGTATCCTATATCTAAGTTATTA CATGTAAGGACAAGGAGGGTCGGGGCGATGAGGTGAGGCCAATGTATCCTATATCTAAGTTATTA A G WFDC1 Ensembl:ENSG00000103175 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:84309231..84309474 26863196 MeRIP-seq:(Medium) rs967791183 Functional Loss SNV dbSNP153 33..33 33 - - - 78914 RMVar_ID_78914 Human_SNP_ID_612237947 m1A Human chr16 - 84496425 84496425 84496425 CGGAAGGAAGAGGCTCCCCTGTACAGAGACGGAGGGAGGGGTAGCTCCAAAGCCAAAAGAAGAGG CGGAAGGAAGAGGCTCCCCTGTACAGAGACGGCGGGAGGGGTAGCTCCAAAGCCAAAAGAAGAGG T G MEAK7 Ensembl:ENSG00000140950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84496423..84496515 26863196 MeRIP-seq:(Medium) rs1262523190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20425,RMVar_hsa_circ_82373,RMVar_hsa_circ_180309,RMVar_hsa_circ_336896,RMVar_hsa_circ_36007 78915 RMVar_ID_78915 Human_SNP_ID_612241550 m1A Human chr16 - 84504954 84504954 84504954 CTGGCTACTCCGCTCCAGCGCCCAGCCCAGACACCCCTTCTCCCCAGGTACCACTGCTGGCCTGG CTGGCTACTCCGCTCCAGCGCCCAGCCCAGACGCCCCTTCTCCCCAGGTACCACTGCTGGCCTGG T C MEAK7 Ensembl:ENSG00000140950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:84504905..84505020 26863196 MeRIP-seq:(Medium) rs1396560690 Functional Loss SNV dbSNP153 33..33 33 - - - 78916 RMVar_ID_78916 Human_SNP_ID_612264191 m1A Human chr16 + 84566708 84566708 84566708 CTAAGGGAAGCGGGAAGGTGGGGGCTGTGGACACAGGGTGGCGGGCGCTGCCTCTCATGGCTTCT CTAAGGGAAGCGGGAAGGTGGGGGCTGTGGACGCAGGGTGGCGGGCGCTGCCTCTCATGGCTTCT A G lnc-KLHL36-2 RNACentral:URS00008B3CF4 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:84566551..84566850 26863196 MeRIP-seq:(Medium) rs41291692 Functional Loss SNV dbSNP153 33..33 33 - - - 78917 RMVar_ID_78917 Human_SNP_ID_612264205 m1A Human chr16 + 84566732 84566732 84566732 CTGTGGACACAGGGTGGCGGGCGCTGCCTCTCATGGCTTCTTTTCTCCCTGGTGGGCTGGTGGGC CTGTGGACACAGGGTGGCGGGCGCTGCCTCTCGTGGCTTCTTTTCTCCCTGGTGGGCTGGTGGGC A G lnc-KLHL36-2 RNACentral:URS00008B3CF4 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:84566668..84566798 26863196 MeRIP-seq:(Medium) rs1405973939 Functional Loss SNV dbSNP153 33..33 33 - - - 78918 RMVar_ID_78918 Human_SNP_ID_612264307 m1A Human chr16 - 84566901 84566901 84566901 TCAGTGATCGGAAGGAGCTGGAGGAAGATTTCATCAAGAGCGAGCTGAAGAAGGCGGGGGGAGCC TCAGTGATCGGAAGGAGCTGGAGGAAGATTTCGTCAAGAGCGAGCTGAAGAAGGCGGGGGGAGCC T C COTL1 Ensembl:ENSG00000103187 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84566851..84566986 32194978 MeRIP-seq:(Medium) rs377452050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44225,Human_RBP_ID_4386620,Human_RBP_ID_6542683,Human_RBP_ID_8187863,Human_RBP_ID_8440308,Human_RBP_ID_18190564,Human_RBP_ID_26443981,Human_RBP_ID_27446179 Human_Splice_Rec_1746406,Human_Splice_Rec_1746410,Human_Splice_Rec_1746412 RMVar_hsa_circ_77935,RMVar_hsa_circ_91684,RMVar_hsa_circ_108047,RMVar_hsa_circ_82122,RMVar_hsa_circ_180313,RMVar_hsa_circ_180314,RMVar_hsa_circ_180315,RMVar_hsa_circ_180312 78919 RMVar_ID_78919 Human_SNP_ID_612273257 m1A Human chr16 + 84594860 84594860 84594860 GCCTCTCTCTCTTCTCAGTGTCGCCCCCTCCCACGGCTCTGGCTGGCTCCTCTGCGGAGCTCCAT GCCTCTCTCTCTTCTCAGTGTCGCCCCCTCCCGCGGCTCTGGCTGGCTCCTCTGCGGAGCTCCAT A G AC092145.1 Ensembl:ENSG00000261471 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84594857..84594922 26863196 MeRIP-seq:(Medium) rs1352185857 Functional Loss SNV dbSNP153 33..33 33 - - - 78920 RMVar_ID_78920 Human_SNP_ID_612273800 m1A Human chr16 - 84596539 84596539 84596539 GCATGGAGAAGATGCTGTTGGCTTTGGCAATTAGGAGGCCCCTGTGGACCCCTGAGGGCAGTTTC GCATGGAGAAGATGCTGTTGGCTTTGGCAATTGGGAGGCCCCTGTGGACCCCTGAGGGCAGTTTC T C COTL1 Ensembl:ENSG00000103187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84596537..84596831 26863196 MeRIP-seq:(Medium) rs570010044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2486873 RMVar_hsa_circ_77935,RMVar_hsa_circ_108047,RMVar_hsa_circ_80335,RMVar_hsa_circ_180314,RMVar_hsa_circ_180315,RMVar_hsa_circ_180316 78921 RMVar_ID_78921 Human_SNP_ID_612280907 m1A Human chr16 - 84617898 84617898 84617898 CTGCGGCTCCGCGGCGATGGCCACCAAGATCGACAAAGAGGCTTGCCGGGCGGCGTACAACCTGG CTGCGGCTCCGCGGCGATGGCCACCAAGATCGGCAAAGAGGCTTGCCGGGCGGCGTACAACCTGG T C COTL1 Ensembl:ENSG00000103187 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:84617773..84618075 26863196 MeRIP-seq:(Medium) rs1226140702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44228,Human_RBP_ID_4394036,Human_RBP_ID_18190103,Human_RBP_ID_26950345,Human_RBP_ID_27446182 Human_Splice_Rec_1746401,Human_Splice_Rec_1746407 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 78922 RMVar_ID_78922 Human_SNP_ID_612280924 m1A Human chr16 + 84617923 84617923 84617923 CTCTTTGTCGATCTTGGTGGCCATCGCCGCGGAGCCGCAGCGGGACACTGTCCGGGGCGGCCGAG CTCTTTGTCGATCTTGGTGGCCATCGCCGCGGCGCCGCAGCGGGACACTGTCCGGGGCGGCCGAG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr16:84617876..84618075 26863196 MeRIP-seq:(Medium) rs1181808539 Functional Loss SNV dbSNP153 33..33 33 - - - 78923 RMVar_ID_78923 Human_SNP_ID_612280972 m1A Human chr16 + 84617996 84617996 84617996 TGGCCGGCGGCGGGGATGGGAGCGCGGCGGGTACGCGCCGAGGGCGCACGGGCTGGCGGCGGTGG TGGCCGGCGGCGGGGATGGGAGCGCGGCGGGTGCGCGCCGAGGGCGCACGGGCTGGCGGCGGTGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:84617876..84618100 26863410 MeRIP-seq:(Medium) rs1357090977 Functional Loss SNV dbSNP153 33..33 33 - - - 78924 RMVar_ID_78924 Human_SNP_ID_612280987 m1A Human chr16 - 84618026 84618026 84618026 TCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGCCCGTGCGCCCTCGGCGCGTAC TCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCGCCGCCGCCAGCCCGTGCGCCCTCGGCGCGTAC T C COTL1 Ensembl:ENSG00000103187 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:84617851..84618075;chr16:84617803..84618075;chr16:84617788..84618075 26863196 MeRIP-seq:(Medium) rs959891765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233378,Human_RBP_ID_4386644 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 78925 RMVar_ID_78925 Human_SNP_ID_612281003 m1A Human chr16 - 84618047 84618047 84618047 CAGTGGAAGCCGCCGCCGCGCTCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGC CAGTGGAAGCCGCCGCCGCGCTCGCAGCTTGCGGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGC T C COTL1 Ensembl:ENSG00000103187 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:84617975..84618063 26863410 MeRIP-seq:(Medium) rs567600273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233378,Human_RBP_ID_4394037,Human_RBP_ID_22532833 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 78926 RMVar_ID_78926 Human_SNP_ID_612281004 m1A Human chr16 - 84618047 84618047 84618047 CAGTGGAAGCCGCCGCCGCGCTCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGC CAGTGGAAGCCGCCGCCGCGCTCGCAGCTTGCCGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGC T G COTL1 Ensembl:ENSG00000103187 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:84617975..84618063 26863410 MeRIP-seq:(Medium) rs567600273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233378,Human_RBP_ID_4394037,Human_RBP_ID_22532833 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 78927 RMVar_ID_78927 Human_SNP_ID_612281007 m1A Human chr16 + 84618051 84618051 84618051 GCGGCGGTGGCGACGGCTACGCGGCGCCTGCAAGCTGCGAGCGCGGCGGCGGCTTCCACTGCGGA GCGGCGGTGGCGACGGCTACGCGGCGCCTGCATGCTGCGAGCGCGGCGGCGGCTTCCACTGCGGA A T - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:84617975..84618058 26863410 MeRIP-seq:(Medium) rs1485468465 Functional Loss SNV dbSNP153 33..33 33 - - - 78928 RMVar_ID_78928 Human_SNP_ID_612292003 m1A Human chr16 + 84648593 84648593 84648593 GGGGTCTCCTGAACCCGGGCCCCGCCGCCCCGACCGCCCGGCCCCGCCGCCGGGGCTGTCCCCGC GGGGTCTCCTGAACCCGGGCCCCGCCGCCCCGCCCGCCCGGCCCCGCCGCCGGGGCTGTCCCCGC A C KLHL36 Ensembl:ENSG00000135686 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:84648565..84648886;chr16:84648562..84648723 26863196 MeRIP-seq:(Medium) rs902054898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393285,Human_RBP_ID_22532714 Human_Splice_Rec_1746417,Human_Splice_Rec_1746425 RMVar_hsa_circ_126740,RMVar_hsa_circ_180317 78929 RMVar_ID_78929 Human_SNP_ID_612292116 m1A Human chr16 - 84648882 84648882 84648882 GGACGGCCCGGGGCGGGGGCCACTCACCTGCCACGCGCGGGGCGGTCCGCACAGGCCGCACCTGT GGACGGCCCGGGGCGGGGGCCACTCACCTGCCTCGCGCGGGGCGGTCCGCACAGGCCGCACCTGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:84648836..84648953 26863196 MeRIP-seq:(Medium) rs11866612 Functional Loss SNV dbSNP153 33..33 33 - - - 78930 RMVar_ID_78930 Human_SNP_ID_612297066 m1A Human chr16 + 84662446 84662446 84662446 ACTGTCCCCCTGAGAGTAGCTGGCACGTGGGTAACACAGAAATTTCTGTAGTGAAGCTTGGGCCT ACTGTCCCCCTGAGAGTAGCTGGCACGTGGGTTACACAGAAATTTCTGTAGTGAAGCTTGGGCCT A T KLHL36 Ensembl:ENSG00000135686 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17755862 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9506,GWAS_ID_9507 78931 RMVar_ID_78931 Human_SNP_ID_612309377 m1A Human chr16 + 84700040 84700040 84700040 ATGTGCGGGCGAGAAGATGGCGGCGGCGGGGGAAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTC ATGTGCGGGCGAGAAGATGGCGGCGGCGGGGGGAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTC A G USP10 Ensembl:ENSG00000103194 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84699976..84700176 26863196 MeRIP-seq:(Medium) rs1049318683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763511,Human_RBP_ID_4386800,Human_RBP_ID_5316719,Human_RBP_ID_8812502,Human_RBP_ID_9285950,Human_RBP_ID_9326109,Human_RBP_ID_12829297,Human_RBP_ID_22053490,Human_RBP_ID_22441138,Human_RBP_ID_23114116,Human_RBP_ID_26329273,Human_RBP_ID_27446217 Human_Splice_Rec_1746449,Human_Splice_Rec_1746475,Human_Splice_Rec_1746483,Human_Splice_Rec_1746489,Human_Splice_Rec_1746495,Human_Splice_Rec_1746507,Human_Splice_Rec_1746527,Human_Splice_Rec_1746529,Human_Splice_Rec_1746537,Human_Splice_Rec_1746559,Human_Splice_Rec_1746587,Human_Splice_Rec_1746595,Human_Splice_Rec_1746613 78932 RMVar_ID_78932 Human_SNP_ID_612309378 m1A Human chr16 + 84700041 84700041 84700041 TGTGCGGGCGAGAAGATGGCGGCGGCGGGGGAAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTCC TGTGCGGGCGAGAAGATGGCGGCGGCGGGGGAGGCAGCGTGAGCAGCCGGAGGATCGCGGAGTCC A G USP10 Ensembl:ENSG00000103194 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:84700015..84700142;chr16:84699976..84704755 26863196 MeRIP-seq:(Medium) rs369382426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763511,Human_RBP_ID_4386800,Human_RBP_ID_5316719,Human_RBP_ID_8812502,Human_RBP_ID_9285950,Human_RBP_ID_9326109,Human_RBP_ID_12829297,Human_RBP_ID_22053490,Human_RBP_ID_22441138,Human_RBP_ID_23114116,Human_RBP_ID_26329273,Human_RBP_ID_27446217 Human_Splice_Rec_1746449,Human_Splice_Rec_1746475,Human_Splice_Rec_1746483,Human_Splice_Rec_1746489,Human_Splice_Rec_1746495,Human_Splice_Rec_1746507,Human_Splice_Rec_1746527,Human_Splice_Rec_1746529,Human_Splice_Rec_1746537,Human_Splice_Rec_1746559,Human_Splice_Rec_1746587,Human_Splice_Rec_1746595,Human_Splice_Rec_1746613 78933 RMVar_ID_78933 Human_SNP_ID_612309379 m1A Human chr16 + 84700041 84700041 84700041 TGTGCGGGCGAGAAGATGGCGGCGGCGGGGGAAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTCC TGTGCGGGCGAGAAGATGGCGGCGGCGGGGGATGCAGCGTGAGCAGCCGGAGGATCGCGGAGTCC A T USP10 Ensembl:ENSG00000103194 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:84700015..84700142;chr16:84699976..84704755 26863196 MeRIP-seq:(Medium) rs369382426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763511,Human_RBP_ID_4386800,Human_RBP_ID_5316719,Human_RBP_ID_8812502,Human_RBP_ID_9285950,Human_RBP_ID_9326109,Human_RBP_ID_12829297,Human_RBP_ID_22053490,Human_RBP_ID_22441138,Human_RBP_ID_23114116,Human_RBP_ID_26329273,Human_RBP_ID_27446217 Human_Splice_Rec_1746449,Human_Splice_Rec_1746475,Human_Splice_Rec_1746483,Human_Splice_Rec_1746489,Human_Splice_Rec_1746495,Human_Splice_Rec_1746507,Human_Splice_Rec_1746527,Human_Splice_Rec_1746529,Human_Splice_Rec_1746537,Human_Splice_Rec_1746559,Human_Splice_Rec_1746587,Human_Splice_Rec_1746595,Human_Splice_Rec_1746613 78934 RMVar_ID_78934 Human_SNP_ID_612309566 m1A Human chr16 + 84700381 84700356 84700381 GGCCCCGCTTGGGGAGGGCGTGGAGGGCGCCGAAGGGGTTAACCTCCCTGGGGCTGGACCGCGGG GGCCCCGC_________________________AGGGGTTAACCTCCCTGGGGCTGGACCGCGGG CTTGGGGAGGGCGTGGAGGGCGCCGA C USP10 Ensembl:ENSG00000103194 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84700376..84700532 26863196 MeRIP-seq:(Medium) rs1229239391 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_3502820,Human_RBP_ID_5358562,Human_RBP_ID_8184842,Human_RBP_ID_9419950,Human_RBP_ID_18458601 78935 RMVar_ID_78935 Human_SNP_ID_612309573 m1A Human chr16 + 84700381 84700381 84700381 GGCCCCGCTTGGGGAGGGCGTGGAGGGCGCCGAAGGGGTTAACCTCCCTGGGGCTGGACCGCGGG GGCCCCGCTTGGGGAGGGCGTGGAGGGCGCCGCAGGGGTTAACCTCCCTGGGGCTGGACCGCGGG A C USP10 Ensembl:ENSG00000103194 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:84700376..84700532 26863196 MeRIP-seq:(Medium) rs1328577483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502820,Human_RBP_ID_5358562,Human_RBP_ID_8184842,Human_RBP_ID_9419950,Human_RBP_ID_18458601 78936 RMVar_ID_78936 Human_SNP_ID_612325710 m1A Human chr16 + 84744955 84744955 84744955 GAGCGTAAAAAGAAGAAAAAGCGGCCACCTGGATATTACAGCTATTTGAAAGATGGTGGCGATGA GAGCGTAAAAAGAAGAAAAAGCGGCCACCTGGTTATTACAGCTATTTGAAAGATGGTGGCGATGA A T USP10 Ensembl:ENSG00000103194 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84744843..84745094 32194978 MeRIP-seq:(Medium) rs1345433468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480773,Human_RBP_ID_892692,Human_RBP_ID_4386824,Human_RBP_ID_9066177,Human_RBP_ID_18685634,Human_RBP_ID_26950414,Human_RBP_ID_27246750,Human_RBP_ID_27446234 Human_miRNA_ID_3099562 RMVar_hsa_circ_108263,RMVar_hsa_circ_310179,RMVar_hsa_circ_348800,RMVar_hsa_circ_305159,RMVar_hsa_circ_180324,RMVar_hsa_circ_339590,RMVar_hsa_circ_180321,RMVar_hsa_circ_180322,RMVar_hsa_circ_180320,RMVar_hsa_circ_370478,RMVar_hsa_circ_270993,RMVar_hsa_circ_273393,RMVar_hsa_circ_180325,RMVar_hsa_circ_332026,RMVar_hsa_circ_180323 78937 RMVar_ID_78937 Human_SNP_ID_612325746 m1A Human chr16 + 84745030 84745028 84745031 ACAGAAGCCCTGGTCAATGGCCATGCCAATTCAGCAGTCCCGAACAGTGTCAGTGCAGAGGATGC ACAGAAGCCCTGGTCAATGGCCATGCCAATT___CAGTCCCGAACAGTGTCAGTGCAGAGGATGC TCAG T USP10 Ensembl:ENSG00000103194 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84744994..84745126 26863196 MeRIP-seq:(Medium) rs749035076 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9326113,Human_RBP_ID_18984357,Human_RBP_ID_26950416,Human_RBP_ID_27246750 Human_miRNA_ID_1343769 RMVar_hsa_circ_108263,RMVar_hsa_circ_310179,RMVar_hsa_circ_348800,RMVar_hsa_circ_305159,RMVar_hsa_circ_180324,RMVar_hsa_circ_339590,RMVar_hsa_circ_180321,RMVar_hsa_circ_180322,RMVar_hsa_circ_180320,RMVar_hsa_circ_370478,RMVar_hsa_circ_270993,RMVar_hsa_circ_273393,RMVar_hsa_circ_180325,RMVar_hsa_circ_332026,RMVar_hsa_circ_180323 78938 RMVar_ID_78938 Human_SNP_ID_612325748 m1A Human chr16 + 84745030 84745030 84745030 ACAGAAGCCCTGGTCAATGGCCATGCCAATTCAGCAGTCCCGAACAGTGTCAGTGCAGAGGATGC ACAGAAGCCCTGGTCAATGGCCATGCCAATTCGGCAGTCCCGAACAGTGTCAGTGCAGAGGATGC A G USP10 Ensembl:ENSG00000103194 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84744994..84745126 26863196 MeRIP-seq:(Medium) rs1400147940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326113,Human_RBP_ID_18984357,Human_RBP_ID_26950416,Human_RBP_ID_27246750 Human_miRNA_ID_1343769 RMVar_hsa_circ_108263,RMVar_hsa_circ_310179,RMVar_hsa_circ_348800,RMVar_hsa_circ_305159,RMVar_hsa_circ_180324,RMVar_hsa_circ_339590,RMVar_hsa_circ_180321,RMVar_hsa_circ_180322,RMVar_hsa_circ_180320,RMVar_hsa_circ_370478,RMVar_hsa_circ_270993,RMVar_hsa_circ_273393,RMVar_hsa_circ_180325,RMVar_hsa_circ_332026,RMVar_hsa_circ_180323 78939 RMVar_ID_78939 Human_SNP_ID_612407644 m1A Human chr16 - 84975681 84975681 84975681 TGTCAAAATTGCCAGTGTTGTTTAGGCAATGTAACATTTACCGGCTGTGTACAGCAAACAAGCTA TGTCAAAATTGCCAGTGTTGTTTAGGCAATGTGACATTTACCGGCTGTGTACAGCAAACAAGCTA T C ZDHHC7 Ensembl:ENSG00000153786 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84975631..84975738 26863196 MeRIP-seq:(Medium) rs962519130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1523704,Human_RBP_ID_5288810,Human_RBP_ID_8810838,Human_RBP_ID_9066204,Human_RBP_ID_18288016,Human_RBP_ID_23703776,Human_RBP_ID_27446299 Human_miRNA_ID_1203162 RMVar_hsa_circ_122909,RMVar_hsa_circ_180344 78940 RMVar_ID_78940 Human_SNP_ID_612420116 m1A Human chr16 - 85011402 85011402 85011402 ACCAAGCCGAGCCGAGCCGCGGGGCCCGCTCCAGCCCGGCCATGAGCGCGGCCGCATGATGCGTC ACCAAGCCGAGCCGAGCCGCGGGGCCCGCTCCGGCCCGGCCATGAGCGCGGCCGCATGATGCGTC T C ZDHHC7 Ensembl:ENSG00000153786 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2270847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128681,Human_RBP_ID_4393290,Human_RBP_ID_18418802,Human_RBP_ID_22441624 78941 RMVar_ID_78941 Human_SNP_ID_612420119 m1A Human chr16 + 85011405 85011405 85011405 GCATCATGCGGCCGCGCTCATGGCCGGGCTGGAGCGGGCCCCGCGGCTCGGCTCGGCTTGGTCCC GCATCATGCGGCCGCGCTCATGGCCGGGCTGGCGCGGGCCCCGCGGCTCGGCTCGGCTTGGTCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85011356..85011462 26863196 MeRIP-seq:(Medium) rs1445516677 Functional Loss SNV dbSNP153 33..33 33 - - - 78942 RMVar_ID_78942 Human_SNP_ID_612494990 m1A Human chr16 + 85230912 85230912 85230912 CAGAGGGATGGGTGGAAGGATGGATAGAATGGAATGGATGGATGGATGAATGAATGGATGGACAG CAGAGGGATGGGTGGAAGGATGGATAGAATGGGATGGATGGATGGATGAATGAATGGATGGACAG A G GSE1,AC092275.1 Ensembl:ENSG00000131149,Ensembl:ENSG00000287787 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85230875..85231026 26863196 MeRIP-seq:(Medium) rs571797302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8440621 78943 RMVar_ID_78943 Human_SNP_ID_612495123 m1A Human chr16 - 85231127 85231127 85231127 ATCCATCCTTCCATCCATCCATCCATCCTTCCATCCATCCTTTCATCCATCCATTCATCTGTCCA ATCCATCCTTCCATCCATCCATCCATCCTTCCTTCCATCCTTTCATCCATCCATTCATCTGTCCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85231125..85231328 26863196 MeRIP-seq:(Medium) rs12598694 Functional Loss SNV dbSNP153 33..33 33 - - - 78944 RMVar_ID_78944 Human_SNP_ID_612495124 m1A Human chr16 - 85231127 85231127 85231127 ATCCATCCTTCCATCCATCCATCCATCCTTCCATCCATCCTTTCATCCATCCATTCATCTGTCCA ATCCATCCTTCCATCCATCCATCCATCCTTCCCTCCATCCTTTCATCCATCCATTCATCTGTCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85231125..85231328 26863196 MeRIP-seq:(Medium) rs12598694 Functional Loss SNV dbSNP153 33..33 33 - - - 78945 RMVar_ID_78945 Human_SNP_ID_612542441 m1A Human chr16 - 85371222 85371222 85371222 GGCTCTTCTGGTCCATGAGCACTGCCTGGCCCAGCCCCTGGCCCCCCTGCCCTGGCCTGGTAGCC GGCTCTTCTGGTCCATGAGCACTGCCTGGCCCGGCCCCTGGCCCCCCTGCCCTGGCCTGGTAGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85371171..85371348 26863196 MeRIP-seq:(Medium) rs1040008227 Functional Loss SNV dbSNP153 33..33 33 - - - 78946 RMVar_ID_78946 Human_SNP_ID_612543747 m1A Human chr16 - 85375335 85375335 85375335 CCTGCTCATCTGAGACTCCTGCATTGCCCCTCACCTGGGGGAGGTGAGGTGACTTGGCAGGGCCA CCTGCTCATCTGAGACTCCTGCATTGCCCCTCGCCTGGGGGAGGTGAGGTGACTTGGCAGGGCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85375288..85375382 26863196 MeRIP-seq:(Medium) rs1432225911 Functional Loss SNV dbSNP153 33..33 33 - - - 78947 RMVar_ID_78947 Human_SNP_ID_612547911 m1A Human chr16 + 85387840 85387840 85387840 AGACAAATGGGTGAATGAAAATGGATGGGTGTATGTTTGCATGGACGGATGATTGGATGATTGGT AGACAAATGGGTGAATGAAAATGGATGGGTGTGTGTTTGCATGGACGGATGATTGGATGATTGGT A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85387789..85387914 26863196 MeRIP-seq:(Medium) rs568502968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22943093,Human_RBP_ID_23704174 78948 RMVar_ID_78948 Human_SNP_ID_612548091 m1A Human chr16 + 85388151 85388151 85388151 GACGGATGGATGGATGGATGTATGGATTGGTGAATGAATGGGTGAGTGGGTGGATGGGTGGGTGG GACGGATGGATGGATGGATGTATGGATTGGTGGATGAATGGGTGAGTGGGTGGATGGGTGGGTGG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:85388033..85388267 26863196 MeRIP-seq:(Medium) rs1448407460 Functional Loss SNV dbSNP153 33..33 33 - - - 78949 RMVar_ID_78949 Human_SNP_ID_612548439 m1A Human chr16 - 85388721 85388710 85388722 ATCTTTCCTTCCTTCCTTCCATCCACCCATCTATCCACTCATCCACCCATCCATCCATCTACTCA ATCTTTCCTTCCTTCCTTCCATCCACCCATC____________CACCCATCCATCCATCTACTCA GGATGAGTGGATA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:85388586..85388959;chr16:85388523..85388894 26863196 MeRIP-seq:(Medium) rs1476083553 Functional Loss DEL dbSNP153 32..43 33 - - - 78950 RMVar_ID_78950 Human_SNP_ID_612548507 m1A Human chr16 + 85388981 85388981 85388981 GAAGTGTTCTTTGGGAATAGATCATGAAGGAAAAAAAAGAGAGAGAAATGTTCCACGATGTTGAG GAAGTGTTCTTTGGGAATAGATCATGAAGGAAGAAAAAGAGAGAGAAATGTTCCACGATGTTGAG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85388930..85389077 26863196 MeRIP-seq:(Medium) rs1451244782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23704189 78951 RMVar_ID_78951 Human_SNP_ID_612550317 m1A Human chr16 - 85394743 85394742 85394744 GAGGAAAGGTTTGCTCTGCTGTAGAAAAAGAGATGTTCTCGGGGGAGACGGACGGGGCTTCTGCT GAGGAAAGGTTTGCTCTGCTGTAGAAAAAGA__TGTTCTCGGGGGAGACGGACGGGGCTTCTGCT ATC A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:85394722..85394864 26863196 MeRIP-seq:(Medium) rs1179098446 Functional Loss DEL dbSNP153 32..33 33 - - - 78952 RMVar_ID_78952 Human_SNP_ID_612550411 m1A Human chr16 - 85395096 85395096 85395096 TCATCCTCAGCTTTGTGTGGCTGCAGCCTACAACCTCCCTATGCTTAGGTGCCCCAGTCTCTGCC TCATCCTCAGCTTTGTGTGGCTGCAGCCTACAGCCTCCCTATGCTTAGGTGCCCCAGTCTCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85395046..85395195 26863196 MeRIP-seq:(Medium) rs894732180 Functional Loss SNV dbSNP153 33..33 33 - - - 78953 RMVar_ID_78953 Human_SNP_ID_612560803 m1A Human chr16 + 85418844 85418844 85418844 GGGAGGGATTGGATTTGGGAAACGTTTTGAGCATAGAGCTGTCAGGATTTGCTGGCGGAGCAGAG GGGAGGGATTGGATTTGGGAAACGTTTTGAGCGTAGAGCTGTCAGGATTTGCTGGCGGAGCAGAG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85418765..85419107 26863196 MeRIP-seq:(Medium) rs1475965025 Functional Loss SNV dbSNP153 33..33 33 - - - 78954 RMVar_ID_78954 Human_SNP_ID_612562332 m1A Human chr16 - 85422529 85422529 85422529 GCCCACAGTGGCTGCTCCGTGAACGTGTGTACAAGGGGACTCCCGCACGCTGCTCCTCCTCCTCC GCCCACAGTGGCTGCTCCGTGAACGTGTGTACGAGGGGACTCCCGCACGCTGCTCCTCCTCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85422478..85422718 26863196 MeRIP-seq:(Medium) rs1016821906 Functional Loss SNV dbSNP153 33..33 33 - - - 78955 RMVar_ID_78955 Human_SNP_ID_612563270 m1A Human chr16 - 85425384 85425384 85425384 TCCAAGGTCAGTCCCAGATCCATCCTCCACCAAGCCTCTGGGTCCAGCAACTCCACCCTTTCCCT TCCAAGGTCAGTCCCAGATCCATCCTCCACCAGGCCTCTGGGTCCAGCAACTCCACCCTTTCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85425334..85425421 26863196 MeRIP-seq:(Medium) rs1028037433 Functional Loss SNV dbSNP153 33..33 33 - - - 78956 RMVar_ID_78956 Human_SNP_ID_612563595 m1A Human chr16 + 85426120 85426120 85426120 TGAATGAGAGGGAGGGAGGAAGGAAGGAAGGAAGGAAGGGTAGATGTATGTATGGATGGATGAAT TGAATGAGAGGGAGGGAGGAAGGAAGGAAGGATGGAAGGGTAGATGTATGTATGGATGGATGAAT A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85426073..85426411 26863196 MeRIP-seq:(Medium) rs1423545928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23704319 78957 RMVar_ID_78957 Human_SNP_ID_612563600 m1A Human chr16 - 85426128 85426128 85426128 ACCCATCCATTCATCCATCCATACATACATCTACCCTTCCTTCCTTCCTTCCTTCCTCCCTCCCT ACCCATCCATTCATCCATCCATACATACATCTTCCCTTCCTTCCTTCCTTCCTTCCTCCCTCCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85426077..85426407 26863196 MeRIP-seq:(Medium) rs1567477250 Functional Loss SNV dbSNP153 33..33 33 - - - 78958 RMVar_ID_78958 Human_SNP_ID_612563812 m1A Human chr16 - 85426579 85426562 85426580 ATTTATCCATCCATCCATTCATTCACCCATCCACATTCATTCACCCCCCATCCATCCACCATTCA ATTTATCCATCCATCCATTCATTCACCCATC__________________ATCCATCCACCATTCA TGGGGGGTGAATGAATGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:85426528..85426712 26863196 MeRIP-seq:(Medium) rs1227424508 Functional Loss DEL dbSNP153 32..49 33 - - - 78959 RMVar_ID_78959 Human_SNP_ID_612575409 m1A Human chr16 + 85463789 85463789 85463789 GCCCGCCGAGGGTGGGGAGCGCCATGAGTCCCATCGGAGAGAGGGTGAGCGGGACTCTGAGGCCT GCCCGCCGAGGGTGGGGAGCGCCATGAGTCCCGTCGGAGAGAGGGTGAGCGGGACTCTGAGGCCT A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85463783..85463862 26863196 MeRIP-seq:(Medium) rs937260189 Functional Loss SNV dbSNP153 33..33 33 - - - 78960 RMVar_ID_78960 Human_SNP_ID_612585317 m1A Human chr16 + 85491409 85491409 85491409 AGGAACAGGAGAGGTGGGGTGTTGGAAGATGCAGGGTATTCTGGGGGGCTGGGTGGTGGCTTTAG AGGAACAGGAGAGGTGGGGTGTTGGAAGATGCGGGGTATTCTGGGGGGCTGGGTGGTGGCTTTAG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:85491361..85491556 26863196 MeRIP-seq:(Medium) rs1305719674 Functional Loss SNV dbSNP153 33..33 33 - - - 78961 RMVar_ID_78961 Human_SNP_ID_612585869 m1A Human chr16 + 85493082 85493082 85493082 GGGGACAGCGGAGGCTGGTGGGGGGATGTTGGAGCAGAGGCCTGGAGGAAGGGAGCTGGTGAGCC GGGGACAGCGGAGGCTGGTGGGGGGATGTTGGCGCAGAGGCCTGGAGGAAGGGAGCTGGTGAGCC A C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85493036..85493120 26863196 MeRIP-seq:(Medium) rs1043808203 Functional Loss SNV dbSNP153 33..33 33 - - - 78962 RMVar_ID_78962 Human_SNP_ID_612585870 m1A Human chr16 + 85493082 85493082 85493082 GGGGACAGCGGAGGCTGGTGGGGGGATGTTGGAGCAGAGGCCTGGAGGAAGGGAGCTGGTGAGCC GGGGACAGCGGAGGCTGGTGGGGGGATGTTGGTGCAGAGGCCTGGAGGAAGGGAGCTGGTGAGCC A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85493036..85493120 26863196 MeRIP-seq:(Medium) rs1043808203 Functional Loss SNV dbSNP153 33..33 33 - - - 78963 RMVar_ID_78963 Human_SNP_ID_612589326 m1A Human chr16 + 85502821 85502821 85502821 TCCAGGGATCCTCTGAAACTTGAACAAGATCAACCTGGACTGGAGAGCAGCAGTGGCCCTGGGGA TCCAGGGATCCTCTGAAACTTGAACAAGATCATCCTGGACTGGAGAGCAGCAGTGGCCCTGGGGA A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:85502790..85502926 26863196 MeRIP-seq:(Medium) rs948059132 Functional Loss SNV dbSNP153 33..33 33 - - - 78964 RMVar_ID_78964 Human_SNP_ID_612589363 m1A Human chr16 + 85502897 85502897 85502897 CAGGGGGGTGAAAAAGAGCTGCCTGTTCCAGGAGGCCAGGGCTGGGTGCCCACGGAAGACAGAAT CAGGGGGGTGAAAAAGAGCTGCCTGTTCCAGGGGGCCAGGGCTGGGTGCCCACGGAAGACAGAAT A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85502850..85502992 26863196 MeRIP-seq:(Medium) rs190843789 Functional Loss SNV dbSNP153 33..33 33 - - - 78965 RMVar_ID_78965 Human_SNP_ID_612606204 m1A Human chr16 + 85554336 85554336 85554336 TGAAAGGGAGGCGGCGTGGGGAGGAGAGATACAGGCTCCACACTCACACTCTCTGTGCAGTTGAT TGAAAGGGAGGCGGCGTGGGGAGGAGAGATACGGGCTCCACACTCACACTCTCTGTGCAGTTGAT A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85554326..85554393 26863196 MeRIP-seq:(Medium) rs1166908989 Functional Loss SNV dbSNP153 33..33 33 - - - 78966 RMVar_ID_78966 Human_SNP_ID_612606214 m1A Human chr16 - 85554353 85554351 85554353 TTTGGTTTAAGAAAACGATCAACTGCACAGAGAGTGTGAGTGTGGAGCCTGTATCTCTCCTCCCC TTTGGTTTAAGAAAACGATCAACTGCACAGAG__TGTGAGTGTGGAGCCTGTATCTCTCCTCCCC ACT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85554320..85554473 26863196 MeRIP-seq:(Medium) rs1367985497 Functional Loss DEL dbSNP153 33..34 33 - - - 78967 RMVar_ID_78967 Human_SNP_ID_612606215 m1A Human chr16 - 85554353 85554353 85554353 TTTGGTTTAAGAAAACGATCAACTGCACAGAGAGTGTGAGTGTGGAGCCTGTATCTCTCCTCCCC TTTGGTTTAAGAAAACGATCAACTGCACAGAGTGTGTGAGTGTGGAGCCTGTATCTCTCCTCCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85554320..85554473 26863196 MeRIP-seq:(Medium) rs374832065 Functional Loss SNV dbSNP153 33..33 33 - - - 78968 RMVar_ID_78968 Human_SNP_ID_612606216 m1A Human chr16 - 85554353 85554353 85554353 TTTGGTTTAAGAAAACGATCAACTGCACAGAGAGTGTGAGTGTGGAGCCTGTATCTCTCCTCCCC TTTGGTTTAAGAAAACGATCAACTGCACAGAGCGTGTGAGTGTGGAGCCTGTATCTCTCCTCCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85554320..85554473 26863196 MeRIP-seq:(Medium) rs374832065 Functional Loss SNV dbSNP153 33..33 33 - - - 78969 RMVar_ID_78969 Human_SNP_ID_612606505 m1A Human chr16 - 85555124 85555103 85555125 CGAAAGGGTAGGGGCGCAGCGGCGGGCGGCTGAAGGCGGCGGCGGCGGCGGCTCCTTCCGTCTCT CGAAAGGGTAGGGGCGCAGCGGCGGGCGGCT______________________CCTTCCGTCTCT GAGCCGCCGCCGCCGCCGCCTTC G lnc-GINS2-5 RNACentral:URS0000D5D51B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85555078..85555330 26863196 MeRIP-seq:(Medium) rs1024851066 Functional Loss DEL dbSNP153 32..53 33 - - - 78970 RMVar_ID_78970 Human_SNP_ID_612606520 m1A Human chr16 - 85555124 85555124 85555124 CGAAAGGGTAGGGGCGCAGCGGCGGGCGGCTGAAGGCGGCGGCGGCGGCGGCTCCTTCCGTCTCT CGAAAGGGTAGGGGCGCAGCGGCGGGCGGCTGCAGGCGGCGGCGGCGGCGGCTCCTTCCGTCTCT T G lnc-GINS2-5 RNACentral:URS0000D5D51B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85555078..85555330 26863196 MeRIP-seq:(Medium) rs1422176282 Functional Loss SNV dbSNP153 33..33 33 - - - 78971 RMVar_ID_78971 Human_SNP_ID_612606536 m1A Human chr16 + 85555190 85555190 85555190 TTTCATTAGGGGAGACAAATCTGCTGTCAGGCAGCCAGCTTTCCAATTTACCGATAATGATTCTT TTTCATTAGGGGAGACAAATCTGCTGTCAGGCCGCCAGCTTTCCAATTTACCGATAATGATTCTT A C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85555142..85555326 26863196 MeRIP-seq:(Medium) rs184863792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9066236 78972 RMVar_ID_78972 Human_SNP_ID_612609646 m1A Human chr16 + 85564225 85564225 85564225 AGGAGGTGGCACTAAAAGCAGGCTTTGGAAGTATGGAGCTTCGAGGTGAGTGAGGCTGGGAGGAA AGGAGGTGGCACTAAAAGCAGGCTTTGGAAGTGTGGAGCTTCGAGGTGAGTGAGGCTGGGAGGAA A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85564176..85564287 26863196 MeRIP-seq:(Medium) rs1465781770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2487675 78973 RMVar_ID_78973 Human_SNP_ID_612609659 m1A Human chr16 + 85564265 85564265 85564265 TCGAGGTGAGTGAGGCTGGGAGGAAGGAGGCTAACACAGTGAGGAGGGAGGAACAGAAATAGGGA TCGAGGTGAGTGAGGCTGGGAGGAAGGAGGCTGACACAGTGAGGAGGGAGGAACAGAAATAGGGA A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85564215..85564298 26863196 MeRIP-seq:(Medium) rs1366695106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2487676,Human_RBP_ID_6543570 78974 RMVar_ID_78974 Human_SNP_ID_612622043 m1A Human chr16 + 85601298 85601298 85601298 TGCCGTGTGAGGGGTGGGAGGGGAGCAGCCCCAGGAGAGGAGGCAGCAGGGGTGGGGCAGCCATG TGCCGTGTGAGGGGTGGGAGGGGAGCAGCCCCGGGAGAGGAGGCAGCAGGGGTGGGGCAGCCATG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85601289..85601418 26863196 MeRIP-seq:(Medium) rs1217231445 Functional Loss SNV dbSNP153 33..33 33 - - - 78975 RMVar_ID_78975 Human_SNP_ID_612622073 m1A Human chr16 + 85601405 85601405 85601405 CTTTACTGGCACTGGGAGGGATTGCAGGGGCCAGGCTGGTGGGGAGGAGGCCTTTCAGAATGGGA CTTTACTGGCACTGGGAGGGATTGCAGGGGCCTGGCTGGTGGGGAGGAGGCCTTTCAGAATGGGA A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85601358..85601467 26863196 MeRIP-seq:(Medium) rs976821558 Functional Loss SNV dbSNP153 33..33 33 - - - 78976 RMVar_ID_78976 Human_SNP_ID_612635385 m1A Human chr16 + 85633973 85633973 85633973 CGCTAGGGATGCTTTCCACCGCGACCAGGACCACCGCCACCGTCAACCCCCTCACCCCCTCGCCG CGCTAGGGATGCTTTCCACCGCGACCAGGACCCCCGCCACCGTCAACCCCCTCACCCCCTCGCCG A C GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85613265..85648694 26863196 MeRIP-seq:(Medium) rs74737530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760044,Human_RBP_ID_17371540,Human_RBP_ID_22532715,Human_RBP_ID_22583052,Human_RBP_ID_26811608 Human_Splice_Rec_1747034,Human_Splice_Rec_1747080 RMVar_hsa_circ_83711,RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_275437,RMVar_hsa_circ_373339,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_99924,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_180362,RMVar_hsa_circ_180364,RMVar_hsa_circ_78162,RMVar_hsa_circ_180365,RMVar_hsa_circ_180363,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78977 RMVar_ID_78977 Human_SNP_ID_612635401 m1A Human chr16 + 85633994 85633994 85633994 CGACCAGGACCACCGCCACCGTCAACCCCCTCACCCCCTCGCCGCTCAATGGCGCCCTGGTGCCC CGACCAGGACCACCGCCACCGTCAACCCCCTCCCCCCCTCGCCGCTCAATGGCGCCCTGGTGCCC A C GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85633911..85634152 26863196 MeRIP-seq:(Medium) rs766447038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760044,Human_RBP_ID_4387285,Human_RBP_ID_5465527,Human_RBP_ID_17371540,Human_RBP_ID_22532715,Human_RBP_ID_26811609 Human_Splice_Rec_1747034,Human_Splice_Rec_1747080 RMVar_hsa_circ_83711,RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_275437,RMVar_hsa_circ_373339,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_99924,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_180362,RMVar_hsa_circ_180364,RMVar_hsa_circ_78162,RMVar_hsa_circ_180365,RMVar_hsa_circ_180363,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78978 RMVar_ID_78978 Human_SNP_ID_612635435 m1A Human chr16 + 85634033 85634033 85634033 CGCCGCTCAATGGCGCCCTGGTGCCCAGCGGCAGCCCCGCCACCAGCAGCGCGCTGTCGGCCCAG CGCCGCTCAATGGCGCCCTGGTGCCCAGCGGCGGCCCCGCCACCAGCAGCGCGCTGTCGGCCCAG A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85633987..85634074 26863196 MeRIP-seq:(Medium) rs775406138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760044,Human_RBP_ID_17371540,Human_RBP_ID_22532715 Human_Splice_Rec_1747081 Human_miRNA_ID_2052363,Human_miRNA_ID_2052364,Human_miRNA_ID_2147097,Human_miRNA_ID_2147098,Human_miRNA_ID_2988522,Human_miRNA_ID_2988523,Human_miRNA_ID_3022223,Human_miRNA_ID_3022224,Human_miRNA_ID_3066182,Human_miRNA_ID_3066183 RMVar_hsa_circ_83711,RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_275437,RMVar_hsa_circ_373339,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_99924,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_180362,RMVar_hsa_circ_180364,RMVar_hsa_circ_78162,RMVar_hsa_circ_180365,RMVar_hsa_circ_180363,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78979 RMVar_ID_78979 Human_SNP_ID_612642420 m1A Human chr16 - 85648608 85648608 85648608 CATGGGCACGCGCTTGGGTGTGCTGGCGGGGGAGCTGTGGTTGGTGGCCGGAGAGGACACGGGGG CATGGGCACGCGCTTGGGTGTGCTGGCGGGGGGGCTGTGGTTGGTGGCCGGAGAGGACACGGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85648519..85648655 26863196 MeRIP-seq:(Medium) rs777863962 Functional Loss SNV dbSNP153 33..33 33 - - - 78980 RMVar_ID_78980 Human_SNP_ID_612644454 m1A Human chr16 - 85652567 85652567 85652567 CCAGGAGACAGTCAGCGAGGATTAACTGGAGGAGCCGCCGCCGCCGCCGCCGCCTGGAATCTTCA CCAGGAGACAGTCAGCGAGGATTAACTGGAGGCGCCGCCGCCGCCGCCGCCGCCTGGAATCTTCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85652554..85652694 26863196 MeRIP-seq:(Medium) rs1313570805 Functional Loss SNV dbSNP153 33..33 33 - - - 78981 RMVar_ID_78981 Human_SNP_ID_612645765 m1A Human chr16 + 85654426 85654426 85654426 CCCCTTCGGCCTCTCCCCCAGCTCAGTTGTGCAGGATTCCCGCTTCCCGCCACTCAAGTAAGTTG CCCCTTCGGCCTCTCCCCCAGCTCAGTTGTGCGGGATTCCCGCTTCCCGCCACTCAAGTAAGTTG A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:85654375..85655752 32194978 MeRIP-seq:(Medium) rs1277767607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480874,Human_RBP_ID_761279,Human_RBP_ID_895575,Human_RBP_ID_9285955,Human_RBP_ID_17077997,Human_RBP_ID_17255525,Human_RBP_ID_17371543,Human_RBP_ID_18685828,Human_RBP_ID_18940715 Human_Splice_Rec_1747047,Human_Splice_Rec_1747075,Human_Splice_Rec_1747085,Human_Splice_Rec_1747113,Human_Splice_Rec_1747137 RMVar_hsa_circ_83711,RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_99924,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_180362,RMVar_hsa_circ_78162,RMVar_hsa_circ_180363,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_19811,RMVar_hsa_circ_180355 78982 RMVar_ID_78982 Human_SNP_ID_612646038 m1A Human chr16 + 85654855 85654855 85654855 CCCCCAGTACCGTGACCGAGGACTACCTGAGAAGCTTCCGGCCCTACCACACCACCGACGACCTC CCCCCAGTACCGTGACCGAGGACTACCTGAGAGGCTTCCGGCCCTACCACACCACCGACGACCTC A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85654806..85654931 26863196 MeRIP-seq:(Medium) rs1260019045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1847438,Human_RBP_ID_8440749,Human_RBP_ID_12833421,Human_RBP_ID_18685829 Human_Splice_Rec_1747048,Human_Splice_Rec_1747076,Human_Splice_Rec_1747086,Human_Splice_Rec_1747114,Human_Splice_Rec_1747138 Human_miRNA_ID_2008951 RMVar_hsa_circ_83711,RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_99924,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_180362,RMVar_hsa_circ_78162,RMVar_hsa_circ_180363,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_19811,RMVar_hsa_circ_180355 78983 RMVar_ID_78983 Human_SNP_ID_612646903 m1A Human chr16 + 85656445 85656391 85656445 GACCGCGAGCGGGAGAAGGAACGTGAGCGCGAACGCGAGAAGGAGCGCGAGCAAGAGAAGGAGCG _________________________________CGCGAGAAGGAGCGCGAGCAAGAGAAGGAGCG GCGCGAGCGTGAGCGTGAGGCTGACCGCGAGCGGGAGAAGGAACGTGAGCGCGAA G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85656395..85656525 26863196 MeRIP-seq:(Medium) rs1567736147 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_889997,Human_RBP_ID_9285956,Human_RBP_ID_9374753,Human_RBP_ID_18987059,Human_RBP_ID_22944699,Human_RBP_ID_26329282 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355,RMVar_hsa_circ_64089 78984 RMVar_ID_78984 Human_SNP_ID_612646957 m1A Human chr16 + 85656426 85656426 85656426 CGAGCGTGAGCGTGAGGCTGACCGCGAGCGGGAGAAGGAACGTGAGCGCGAACGCGAGAAGGAGC CGAGCGTGAGCGTGAGGCTGACCGCGAGCGGGCGAAGGAACGTGAGCGCGAACGCGAGAAGGAGC A C GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85654326..85656699 26863196 MeRIP-seq:(Medium) rs749427281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889996,Human_RBP_ID_9285956,Human_RBP_ID_9374753,Human_RBP_ID_18987059,Human_RBP_ID_26329282 Human_Splice_Rec_1747052,Human_Splice_Rec_1747090,Human_Splice_Rec_1747118,Human_Splice_Rec_1747142 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355,RMVar_hsa_circ_64089 78985 RMVar_ID_78985 Human_SNP_ID_612646978 m1A Human chr16 + 85656445 85656445 85656445 GACCGCGAGCGGGAGAAGGAACGTGAGCGCGAACGCGAGAAGGAGCGCGAGCAAGAGAAGGAGCG GACCGCGAGCGGGAGAAGGAACGTGAGCGCGAGCGCGAGAAGGAGCGCGAGCAAGAGAAGGAGCG A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85656395..85656525 26863196 MeRIP-seq:(Medium) rs565614445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889997,Human_RBP_ID_9285956,Human_RBP_ID_9374753,Human_RBP_ID_18987059,Human_RBP_ID_22944699,Human_RBP_ID_26329282 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355,RMVar_hsa_circ_64089 78986 RMVar_ID_78986 Human_SNP_ID_612647053 m1A Human chr16 + 85656516 85656516 85656516 TGAGAAGGAGCGCGAGCGCGAGCTGGAGCGCCAGCGGGAGCAGCGGGCCCGGGAGAAGGAGCTGC TGAGAAGGAGCGCGAGCGCGAGCTGGAGCGCCGGCGGGAGCAGCGGGCCCGGGAGAAGGAGCTGC A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85656351..85656601 26863196 MeRIP-seq:(Medium) rs1446508502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261680,Human_RBP_ID_889997,Human_RBP_ID_3949636,Human_RBP_ID_8812107,Human_RBP_ID_9286438,Human_RBP_ID_9373291,Human_RBP_ID_22944699 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355,RMVar_hsa_circ_64089 78987 RMVar_ID_78987 Human_SNP_ID_612647061 m1A Human chr16 + 85656525 85656525 85656525 GCGCGAGCGCGAGCTGGAGCGCCAGCGGGAGCAGCGGGCCCGGGAGAAGGAGCTGCTGGCCGCCA GCGCGAGCGCGAGCTGGAGCGCCAGCGGGAGCGGCGGGCCCGGGAGAAGGAGCTGCTGGCCGCCA A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85656351..85656576 26863196 MeRIP-seq:(Medium) rs1187038278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889997,Human_RBP_ID_3949636,Human_RBP_ID_8812107,Human_RBP_ID_9286438,Human_RBP_ID_9373291,Human_RBP_ID_22944699 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_120483,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180361,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355,RMVar_hsa_circ_64089 78988 RMVar_ID_78988 Human_SNP_ID_612647530 m1A Human chr16 - 85657453 85657453 85657453 CTCCTGCCGCAGCCGCCGCTGCCGCGCCAGCCACTTCTCCTCCTCATTGGTGCGCTGGATCAGCA CTCCTGCCGCAGCCGCCGCTGCCGCGCCAGCCCCTTCTCCTCCTCATTGGTGCGCTGGATCAGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85657402..85657559 26863196 MeRIP-seq:(Medium) rs759463139 Functional Loss SNV dbSNP153 33..33 33 - - - 78989 RMVar_ID_78989 Human_SNP_ID_612649382 m1A Human chr16 + 85661676 85661676 85661676 GCCCCCAGTGCCACGGGCCCCCGACCCTGCCTACATCTATGATGAGTTCCTGCAGCAGCGCCGGA GCCCCCAGTGCCACGGGCCCCCGACCCTGCCTGCATCTATGATGAGTTCCTGCAGCAGCGCCGGA A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:85657437..85662303 32194978 MeRIP-seq:(Medium) rs776498068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8812112,Human_RBP_ID_9285960 Human_Splice_Rec_1747057,Human_Splice_Rec_1747095,Human_Splice_Rec_1747123,Human_Splice_Rec_1747147,Human_Splice_Rec_1747159 Human_miRNA_ID_2534902,Human_miRNA_ID_2536634,Human_miRNA_ID_3088892 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78990 RMVar_ID_78990 Human_SNP_ID_612649384 m1A Human chr16 + 85661682 85661682 85661682 AGTGCCACGGGCCCCCGACCCTGCCTACATCTATGATGAGTTCCTGCAGCAGCGCCGGAGGCTGG AGTGCCACGGGCCCCCGACCCTGCCTACATCTCTGATGAGTTCCTGCAGCAGCGCCGGAGGCTGG A C GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:85661591..85661721 26863410 MeRIP-seq:(Medium) rs769240026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4404168,Human_RBP_ID_8812112,Human_RBP_ID_9285960 Human_Splice_Rec_1747057,Human_Splice_Rec_1747095,Human_Splice_Rec_1747123,Human_Splice_Rec_1747147,Human_Splice_Rec_1747159 Human_miRNA_ID_2534902,Human_miRNA_ID_2536634,Human_miRNA_ID_3088892 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78991 RMVar_ID_78991 Human_SNP_ID_612649385 m1A Human chr16 + 85661682 85661682 85661682 AGTGCCACGGGCCCCCGACCCTGCCTACATCTATGATGAGTTCCTGCAGCAGCGCCGGAGGCTGG AGTGCCACGGGCCCCCGACCCTGCCTACATCTGTGATGAGTTCCTGCAGCAGCGCCGGAGGCTGG A G GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:85661591..85661721 26863410 MeRIP-seq:(Medium) rs769240026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4404168,Human_RBP_ID_8812112,Human_RBP_ID_9285960 Human_Splice_Rec_1747057,Human_Splice_Rec_1747095,Human_Splice_Rec_1747123,Human_Splice_Rec_1747147,Human_Splice_Rec_1747159 Human_miRNA_ID_2534902,Human_miRNA_ID_2536634,Human_miRNA_ID_3088892 RMVar_hsa_circ_112185,RMVar_hsa_circ_267683,RMVar_hsa_circ_122228,RMVar_hsa_circ_120009,RMVar_hsa_circ_107337,RMVar_hsa_circ_89115,RMVar_hsa_circ_180356,RMVar_hsa_circ_180360,RMVar_hsa_circ_78162,RMVar_hsa_circ_180358,RMVar_hsa_circ_180359,RMVar_hsa_circ_180357,RMVar_hsa_circ_180355 78992 RMVar_ID_78992 Human_SNP_ID_612652709 m1A Human chr16 + 85668348 85668348 85668348 GAGGAGGAAGAGGAGGATGATGAAGATGGAGAAGATGAGGAGGAAGTCCCCAAGCGCAAGTGGCA GAGGAGGAAGAGGAGGATGATGAAGATGGAGATGATGAGGAGGAAGTCCCCAAGCGCAAGTGGCA A T GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85668298..85668447 26863196 MeRIP-seq:(Medium) rs776855998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480883,Human_RBP_ID_1005771,Human_RBP_ID_3949645,Human_RBP_ID_6543635,Human_RBP_ID_18411782,Human_RBP_ID_22944708,Human_RBP_ID_24544422,Human_RBP_ID_26329296,Human_RBP_ID_27811301 Human_Splice_Rec_1747067,Human_Splice_Rec_1747105,Human_Splice_Rec_1747133,Human_Splice_Rec_1747155,Human_Splice_Rec_1747165,Human_Splice_Rec_1747175 RMVar_hsa_circ_89115,RMVar_hsa_circ_180355,RMVar_hsa_circ_373776,RMVar_hsa_circ_180367,RMVar_hsa_circ_180369,RMVar_hsa_circ_280034 78993 RMVar_ID_78993 Human_SNP_ID_612654843 m1A Human chr16 + 85672440 85672440 85672440 TTGAGGAGCCAGAAACAGAAGATGGTCTCAGAAAGGGAGCGGCTCCAGGCAGAACTGGACCACTT TTGAGGAGCCAGAAACAGAAGATGGTCTCAGACAGGGAGCGGCTCCAGGCAGAACTGGACCACTT A C GSE1 Ensembl:ENSG00000131149 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs764148372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480884,Human_RBP_ID_892716,Human_RBP_ID_3948025,Human_RBP_ID_5181562,Human_RBP_ID_9374769,Human_RBP_ID_9444038,Human_RBP_ID_26329300,Human_RBP_ID_27811304 Human_Splice_Rec_1747070,Human_Splice_Rec_1747108,Human_Splice_Rec_1747136,Human_Splice_Rec_1747158,Human_Splice_Rec_1747168,Human_Splice_Rec_1747180,Human_Splice_Rec_1747186,Human_Splice_Rec_1747188 78994 RMVar_ID_78994 Human_SNP_ID_612661912 m1A Human chr16 - 85688898 85688898 85688898 CCGTGAGGCTCTGGCCTGCAGCTCGCGCCGCCATGGACGCTGCCGAGGTCGAATTCCTCGCCGAG CCGTGAGGCTCTGGCCTGCAGCTCGCGCCGCCGTGGACGCTGCCGAGGTCGAATTCCTCGCCGAG T C GINS2 Ensembl:ENSG00000131153 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85688851..85688953 26863196 MeRIP-seq:(Medium) rs905760125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480973,Human_RBP_ID_1523823,Human_RBP_ID_4387577,Human_RBP_ID_12834191,Human_RBP_ID_26810675 Human_Splice_Rec_1747197 RMVar_hsa_circ_112267,RMVar_hsa_circ_180370 78995 RMVar_ID_78995 Human_SNP_ID_612661934 m1A Human chr16 - 85688925 85688925 85688925 TCCGGGACGCTGAGGGGCCCGAGGAGACCGTGAGGCTCTGGCCTGCAGCTCGCGCCGCCATGGAC TCCGGGACGCTGAGGGGCCCGAGGAGACCGTGGGGCTCTGGCCTGCAGCTCGCGCCGCCATGGAC T C GINS2 Ensembl:ENSG00000131153 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:85688826..85688975 26863410 MeRIP-seq:(Medium) rs1567794361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4387577,Human_RBP_ID_18685906,Human_RBP_ID_23704768 Human_miRNA_ID_2209325,Human_miRNA_ID_3033930 RMVar_hsa_circ_112267,RMVar_hsa_circ_180370 78996 RMVar_ID_78996 Human_SNP_ID_612669798 m1A Human chr16 + 85710326 85710326 85710326 ACACATTTGAAAGCCTGAGAAGCCAGGCGTGGAGCACACACGCACGTACACACGACAGAGAGACA ACACATTTGAAAGCCTGAGAAGCCAGGCGTGGGGCACACACGCACGTACACACGACAGAGAGACA A G AC018695.9 Ensembl:ENSG00000287125 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:85710324..85710404 26863196 MeRIP-seq:(Medium) rs1193094771 Functional Loss SNV dbSNP153 33..33 33 - - - 78997 RMVar_ID_78997 Human_SNP_ID_612677217 m1A Human chr16 - 85731345 85731345 85731345 TTTGGCCTTGGAGCAGGGCCAGCTTCACAGGCATGTGACCTCTGCAGCTGCACAGGGCCCCATGC TTTGGCCTTGGAGCAGGGCCAGCTTCACAGGCGTGTGACCTCTGCAGCTGCACAGGGCCCCATGC T C C16orf74 Ensembl:ENSG00000154102 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85731296..85731547 26863196 MeRIP-seq:(Medium) rs1044124047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126907 RMVar_hsa_circ_94666,RMVar_hsa_circ_180374 78998 RMVar_ID_78998 Human_SNP_ID_612684973 m1A Human chr16 - 85750999 85750999 85750999 GCCGCGGCCCCCCGAGCCCGACCGCCGCCGCCACCACCACCAGCGCCCGGGCGGGCCTCGCGCGC GCCGCGGCCCCCCGAGCCCGACCGCCGCCGCCTCCACCACCAGCGCCCGGGCGGGCCTCGCGCGC T A C16orf74 Ensembl:ENSG00000154102 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85750950..85751079 26863196 MeRIP-seq:(Medium) rs1183850383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1747217,Human_Splice_Rec_1747219,Human_Splice_Rec_1747227,Human_Splice_Rec_1747233,Human_Splice_Rec_1747239,Human_Splice_Rec_1747243 78999 RMVar_ID_78999 Human_SNP_ID_612684974 m1A Human chr16 - 85750999 85750999 85750999 GCCGCGGCCCCCCGAGCCCGACCGCCGCCGCCACCACCACCAGCGCCCGGGCGGGCCTCGCGCGC GCCGCGGCCCCCCGAGCCCGACCGCCGCCGCCGCCACCACCAGCGCCCGGGCGGGCCTCGCGCGC T C C16orf74 Ensembl:ENSG00000154102 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85750950..85751079 26863196 MeRIP-seq:(Medium) rs1183850383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1747217,Human_Splice_Rec_1747219,Human_Splice_Rec_1747227,Human_Splice_Rec_1747233,Human_Splice_Rec_1747239,Human_Splice_Rec_1747243 79000 RMVar_ID_79000 Human_SNP_ID_612694332 m1A Human chr16 - 85779537 85779537 85779537 GCAGAATGTTCAGTCGGTCGTGTTTTTAACACAGAGTCTCTAGAAGAGGTGCAGACATCCCGTCT GCAGAATGTTCAGTCGGTCGTGTTTTTAACACGGAGTCTCTAGAAGAGGTGCAGACATCCCGTCT T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:85779380..85779629 32194978 MeRIP-seq:(Medium) rs1440723989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481001,Human_RBP_ID_1005787,Human_RBP_ID_1523827,Human_RBP_ID_1847475,Human_RBP_ID_12834313,Human_RBP_ID_17255548,Human_RBP_ID_17653108,Human_RBP_ID_17882164,Human_RBP_ID_18685919,Human_RBP_ID_27660920 Human_miRNA_ID_2751063,Human_miRNA_ID_2797940,Human_miRNA_ID_2798906,Human_miRNA_ID_2800287,Human_miRNA_ID_2807602,Human_miRNA_ID_2810746,Human_miRNA_ID_2813888,Human_miRNA_ID_2833478,Human_miRNA_ID_2853001,Human_miRNA_ID_2854063,Human_miRNA_ID_2861145 RMVar_hsa_circ_115833,RMVar_hsa_circ_180376,RMVar_hsa_circ_180377 79001 RMVar_ID_79001 Human_SNP_ID_612701032 m1A Human chr16 + 85799210 85799210 85799210 CCTTACGCGGCTTCTGCTTCTCGGCCACCAGGAGCCCGTTGACGGCGCAGTGCGGGTACTTGGCG CCTTACGCGGCTTCTGCTTCTCGGCCACCAGGGGCCCGTTGACGGCGCAGTGCGGGTACTTGGCG A G COX4I1 Ensembl:ENSG00000131143 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:85799160..85799261 32194978 MeRIP-seq:(Medium) rs751095989 Functional Loss SNV dbSNP153 33..33 33 - - - 79002 RMVar_ID_79002 Human_SNP_ID_612701089 m1A Human chr16 + 85799317 85799317 85799317 ACCCCGGGCATGCTGACCCGGGAGGGCCCCGGAGGCCCCTGGGCGCGCGGCTGAGGCCTGGACCC ACCCCGGGCATGCTGACCCGGGAGGGCCCCGGGGGCCCCTGGGCGCGCGGCTGAGGCCTGGACCC A G COX4I1 Ensembl:ENSG00000131143 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85799267..85799550 26863196 MeRIP-seq:(Medium) rs1177878216 Functional Loss SNV dbSNP153 33..33 33 - - - 79003 RMVar_ID_79003 Human_SNP_ID_612701175 m1A Human chr16 - 85799509 85799509 85799509 TTCCGGCGGCGCCGGGCGAGAAGCGCGACTGGAGTCTGGGGCTGCGGCTTCCCAGAGGCGCGAGT TTCCGGCGGCGCCGGGCGAGAAGCGCGACTGGTGTCTGGGGCTGCGGCTTCCCAGAGGCGCGAGT T A EMC8 Ensembl:ENSG00000131148 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:85799408..85799509 26863410 MeRIP-seq:(Medium) rs909527696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1523844,Human_RBP_ID_4387670,Human_RBP_ID_8810910,Human_RBP_ID_9325308,Human_RBP_ID_18419487,Human_RBP_ID_22442241,Human_RBP_ID_27446455 Human_miRNA_ID_3004569 RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 79004 RMVar_ID_79004 Human_SNP_ID_612701297 m1A Human chr16 - 85799754 85799754 85799754 CTGGCGGCGCCGCACCGGCCACCTCCTGTCTCACCTGCCGCCACTGCCCGCCGCGACCGCCCTCT CTGGCGGCGCCGCACCGGCCACCTCCTGTCTCCCCTGCCGCCACTGCCCGCCGCGACCGCCCTCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:85799626..85799863;chr16:85799651..85799854;chr16:85799651..85799828 26863196 MeRIP-seq:(Medium) rs1029165692 Functional Loss SNV dbSNP153 33..33 33 - - - 79005 RMVar_ID_79005 Human_SNP_ID_612701842 m1A Human chr16 + 85801147 85801147 85801147 AAAATTCCAAAATGCTCTGGGGCAAAAAGAAGACTAATTCCTTGCTGTTTGTCCTTATTCATAGA AAAATTCCAAAATGCTCTGGGGCAAAAAGAAGTCTAATTCCTTGCTGTTTGTCCTTATTCATAGA A T COX4I1 Ensembl:ENSG00000131143 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:85801144..85801325 26863410 MeRIP-seq:(Medium) rs985255305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111613,RMVar_hsa_circ_180380 79006 RMVar_ID_79006 Human_SNP_ID_612703463 m1A Human chr16 - 85805823 85805823 85805823 TCTGCCACATGATAACGAGCGCGGTGAAACCGATGAAGAACATGGCACCGCCCACAACCGTCTTC TCTGCCACATGATAACGAGCGCGGTGAAACCGGTGAAGAACATGGCACCGCCCACAACCGTCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr16:85805775..85805907;chr16:85805776..85805825 26863196,32194978 MeRIP-seq:(Medium) rs1348177297 Functional Loss SNV dbSNP153 33..33 33 - - - 79007 RMVar_ID_79007 Human_SNP_ID_612703840 m1A Human chr16 + 85806788 85806788 85806788 AAAGCTTTGACAAAGAGTGGGTGGCCAAGCAGACCAAGAGGATGCTGGACATGAAGGTGAACCCC AAAGCTTTGACAAAGAGTGGGTGGCCAAGCAGTCCAAGAGGATGCTGGACATGAAGGTGAACCCC A T COX4I1 Ensembl:ENSG00000131143 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:85806688..85806937 26863196 MeRIP-seq:(Medium) rs770133953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481037,Human_RBP_ID_1179517,Human_RBP_ID_1523867,Human_RBP_ID_5180842,Human_RBP_ID_6543861,Human_RBP_ID_9066278,Human_RBP_ID_12834817,Human_RBP_ID_17653116,Human_RBP_ID_18685946,Human_RBP_ID_22441633,Human_RBP_ID_23209460,Human_RBP_ID_26444083,Human_RBP_ID_27247482,Human_RBP_ID_27446462 Human_Splice_Rec_1747326,Human_Splice_Rec_1747334,Human_Splice_Rec_1747348,Human_Splice_Rec_1747356,Human_Splice_Rec_1747372,Human_Splice_Rec_1747380 Human_miRNA_ID_2442086 RMVar_hsa_circ_112900,RMVar_hsa_circ_111613,RMVar_hsa_circ_180380,RMVar_hsa_circ_81348,RMVar_hsa_circ_180381,RMVar_hsa_circ_108724,RMVar_hsa_circ_93414,RMVar_hsa_circ_180382,RMVar_hsa_circ_180383,RMVar_hsa_circ_180385 79008 RMVar_ID_79008 Human_SNP_ID_612703843 m1A Human chr16 + 85806797 85806797 85806797 ACAAAGAGTGGGTGGCCAAGCAGACCAAGAGGATGCTGGACATGAAGGTGAACCCCATCCAGGGC ACAAAGAGTGGGTGGCCAAGCAGACCAAGAGGTTGCTGGACATGAAGGTGAACCCCATCCAGGGC A T COX4I1 Ensembl:ENSG00000131143 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85806687..85806933 26863196 MeRIP-seq:(Medium) rs980080098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233610,Human_RBP_ID_481038,Human_RBP_ID_1523867,Human_RBP_ID_1847497,Human_RBP_ID_3949649,Human_RBP_ID_5180843,Human_RBP_ID_6543861,Human_RBP_ID_8440880,Human_RBP_ID_12834817,Human_RBP_ID_17255549,Human_RBP_ID_17653117,Human_RBP_ID_18685947,Human_RBP_ID_20157573,Human_RBP_ID_22441633,Human_RBP_ID_23209460,Human_RBP_ID_23704962,Human_RBP_ID_26950904,Human_RBP_ID_27446462 Human_Splice_Rec_1747326,Human_Splice_Rec_1747334,Human_Splice_Rec_1747348,Human_Splice_Rec_1747356,Human_Splice_Rec_1747372,Human_Splice_Rec_1747380 Human_miRNA_ID_970503,Human_miRNA_ID_2195966,Human_miRNA_ID_2442086 RMVar_hsa_circ_112900,RMVar_hsa_circ_111613,RMVar_hsa_circ_180380,RMVar_hsa_circ_81348,RMVar_hsa_circ_180381,RMVar_hsa_circ_108724,RMVar_hsa_circ_93414,RMVar_hsa_circ_180382,RMVar_hsa_circ_180383,RMVar_hsa_circ_180385 79009 RMVar_ID_79009 Human_SNP_ID_612703853 m1A Human chr16 + 85806832 85806832 85806832 CTGGACATGAAGGTGAACCCCATCCAGGGCTTAGCCTCCAAGTGGGACTACGAAAAGAACGAGTG CTGGACATGAAGGTGAACCCCATCCAGGGCTTCGCCTCCAAGTGGGACTACGAAAAGAACGAGTG A C COX4I1 Ensembl:ENSG00000131143 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85806782..85806945 26863196 MeRIP-seq:(Medium) rs767772859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44747,Human_RBP_ID_233610,Human_RBP_ID_481039,Human_RBP_ID_894853,Human_RBP_ID_1523867,Human_RBP_ID_1847497,Human_RBP_ID_3500974,Human_RBP_ID_3949649,Human_RBP_ID_5496255,Human_RBP_ID_8440880,Human_RBP_ID_9066279,Human_RBP_ID_17653117,Human_RBP_ID_18685948,Human_RBP_ID_22441633,Human_RBP_ID_23209461,Human_RBP_ID_23704962,Human_RBP_ID_26950904,Human_RBP_ID_27446462 Human_Splice_Rec_1747326,Human_Splice_Rec_1747334,Human_Splice_Rec_1747348,Human_Splice_Rec_1747356,Human_Splice_Rec_1747364,Human_Splice_Rec_1747372,Human_Splice_Rec_1747380 Human_miRNA_ID_2479530,Human_miRNA_ID_2615956 RMVar_hsa_circ_112900,RMVar_hsa_circ_111613,RMVar_hsa_circ_180380,RMVar_hsa_circ_81348,RMVar_hsa_circ_180381,RMVar_hsa_circ_108724,RMVar_hsa_circ_93414,RMVar_hsa_circ_180382,RMVar_hsa_circ_180383,RMVar_hsa_circ_180385 79010 RMVar_ID_79010 Human_SNP_ID_612703900 m1A Human chr16 - 85806951 85806951 85806951 TTATTAGCAGTGGTACAACTGTTTGGCATAACAGGTTTCCAGTAAATAGGCATGGAGTTGCATGG TTATTAGCAGTGGTACAACTGTTTGGCATAACGGGTTTCCAGTAAATAGGCATGGAGTTGCATGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:85806901..85807000 32194978 MeRIP-seq:(Medium) rs1050175838 Functional Loss SNV dbSNP153 33..33 33 - - - 79011 RMVar_ID_79011 Human_SNP_ID_612703901 m1A Human chr16 - 85806951 85806951 85806951 TTATTAGCAGTGGTACAACTGTTTGGCATAACAGGTTTCCAGTAAATAGGCATGGAGTTGCATGG TTATTAGCAGTGGTACAACTGTTTGGCATAACCGGTTTCCAGTAAATAGGCATGGAGTTGCATGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:85806901..85807000 32194978 MeRIP-seq:(Medium) rs1050175838 Functional Loss SNV dbSNP153 33..33 33 - - - 79012 RMVar_ID_79012 Human_SNP_ID_612771508 m1A Human chr16 - 86013987 86013987 86013987 TGAAGATGGTGATGGTGGTGATGAAGATGGTGATGATGGTGGTGATGGTGGTGATGATGATGATG TGAAGATGGTGATGGTGGTGATGAAGATGGTGGTGATGGTGGTGATGGTGGTGATGATGATGATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:86013938..86014024;chr16:86013922..86014051;chr16:86013924..86014013 26863196 MeRIP-seq:(Medium) rs1228060863 Functional Loss SNV dbSNP153 33..33 33 - - - 79013 RMVar_ID_79013 Human_SNP_ID_612910807 m1A Human chr16 - 86383374 86383374 86383374 CGCAGGAAGGTGGAGCTTGAGTTGGCCCTGCAAGAGGGGAAGAGGAGTTGGAGTTCCCGTGTGGG CGCAGGAAGGTGGAGCTTGAGTTGGCCCTGCAGGAGGGGAAGAGGAGTTGGAGTTCCCGTGTGGG T C HSALNG0113290 RNACentral:URS0000E9C2C0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86383050..86383567 26863196 MeRIP-seq:(Medium) rs1425154977 Functional Loss SNV dbSNP153 33..33 33 - - - 79014 RMVar_ID_79014 Human_SNP_ID_612940826 m1A Human chr16 - 86456728 86456727 86456729 GAAGGAAGACAGCAAGGAAGGAAGGAAGACAGAAAGAAAGAGAGAGACGAAGAAAGAAAGAAACG GAAGGAAGACAGCAAGGAAGGAAGGAAGACA__AAGAAAGAGAGAGACGAAGAAAGAAAGAAACG TTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86456607..86456863 26863196 MeRIP-seq:(Medium) rs1220551182 Functional Loss DEL dbSNP153 32..33 33 - - - 79015 RMVar_ID_79015 Human_SNP_ID_612943976 m1A Human chr16 - 86464359 86464359 86464359 CCACCACCATCACCATCATTACCATCACCATCACCACCATCACCATCACCACCACCATCACCATC CCACCACCATCACCATCATTACCATCACCATCTCCACCATCACCATCACCACCACCATCACCATC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86464309..86464568 26863196 MeRIP-seq:(Medium) rs1185458980 Functional Loss SNV dbSNP153 33..33 33 - - - 79016 RMVar_ID_79016 Human_SNP_ID_612950357 m1A Human chr16 - 86480355 86480355 86480355 GCTGTGGAGGGATAGATGGGCTTGTGGTGGGAATGATTTTCAGAAAGATTTGCAAGAGATTGATG GCTGTGGAGGGATAGATGGGCTTGTGGTGGGACTGATTTTCAGAAAGATTTGCAAGAGATTGATG T G FENDRR Ensembl:ENSG00000268388 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86480328..86480414 26863196 MeRIP-seq:(Medium) rs770602416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5575106 79017 RMVar_ID_79017 Human_SNP_ID_612953465 m1A Human chr16 - 86489267 86489267 86489267 ATTGCTGGGCTGCTTTCTACCTGAGGAAGTCCACTATGCTTGCTTGTGGAGAGTGGATTGTGTGC ATTGCTGGGCTGCTTTCTACCTGAGGAAGTCCTCTATGCTTGCTTGTGGAGAGTGGATTGTGTGC T A FENDRR Ensembl:ENSG00000268388 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs39528 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9508,GWAS_ID_9509,GWAS_ID_9510,GWAS_ID_9511 79018 RMVar_ID_79018 Human_SNP_ID_612953466 m1A Human chr16 - 86489267 86489267 86489267 ATTGCTGGGCTGCTTTCTACCTGAGGAAGTCCACTATGCTTGCTTGTGGAGAGTGGATTGTGTGC ATTGCTGGGCTGCTTTCTACCTGAGGAAGTCCGCTATGCTTGCTTGTGGAGAGTGGATTGTGTGC T C FENDRR Ensembl:ENSG00000268388 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs39528 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9508,GWAS_ID_9509,GWAS_ID_9510,GWAS_ID_9511 79019 RMVar_ID_79019 Human_SNP_ID_612954001 m1A Human chr16 - 86490816 86490816 86490816 GAGGCCATGGGAAGGGACGGAGGTGGAACAGGACTGGACAGAAGCTGATAAATGGTTGTTGCTGA GAGGCCATGGGAAGGGACGGAGGTGGAACAGGGCTGGACAGAAGCTGATAAATGGTTGTTGCTGA T C FENDRR Ensembl:ENSG00000268388 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86490814..86490881 26863196 MeRIP-seq:(Medium) rs576645636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5575716 RMVar_hsa_circ_332035 79020 RMVar_ID_79020 Human_SNP_ID_612957906 m1A Human chr16 - 86502025 86502025 86502025 ACACAAATGCACACACAGAGAGCGCACAATACAAGCACACGCATACACAGATTCCATTCACATGG ACACAAATGCACACACAGAGAGCGCACAATACGAGCACACGCATACACAGATTCCATTCACATGG T C FENDRR Ensembl:ENSG00000268388 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86502017..86502448 26863196 MeRIP-seq:(Medium) rs1299258104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2488287 79021 RMVar_ID_79021 Human_SNP_ID_612960116 m1A Human chr16 + 86508284 86508284 86508284 CTCTTCTCCCGCGAGCGCAGATCTGGCGGAGGAGGCGGCGACTGCCCGGCAGGCTGCGCCGGCGA CTCTTCTCCCGCGAGCGCAGATCTGGCGGAGGCGGCGGCGACTGCCCGGCAGGCTGCGCCGGCGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86508281..86508372 26863196 MeRIP-seq:(Medium) rs1204441179 Functional Loss SNV dbSNP153 33..33 33 - - - 79022 RMVar_ID_79022 Human_SNP_ID_612960299 m1A Human chr16 + 86508717 86508717 86508717 GCTCCTGCGCTGTCCTGCGCTCCGCTCTCGGCACCACCTTTCGTGGCTCCACCGCCCCCAGCCCG GCTCCTGCGCTGTCCTGCGCTCCGCTCTCGGCGCCACCTTTCGTGGCTCCACCGCCCCCAGCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:86498579..86508899;chr16:86508651..86508850 26863196 MeRIP-seq:(Medium) rs1473869797 Functional Loss SNV dbSNP153 33..33 33 - - - 79023 RMVar_ID_79023 Human_SNP_ID_612960338 m1A Human chr16 - 86508830 86508830 86508830 AGAGCAGACAGCGCGGGCTGGGAGCGCCGGCAAGGGCGGCCCTCGCGCACCTGGCTGCCAGCCCG AGAGCAGACAGCGCGGGCTGGGAGCGCCGGCAGGGGCGGCCCTCGCGCACCTGGCTGCCAGCCCG T C FENDRR Ensembl:ENSG00000268388 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:86508625..86509042;chr16:86508623..86508844 26863196 MeRIP-seq:(Medium) rs756635598 Functional Loss SNV dbSNP153 33..33 33 - - - 79024 RMVar_ID_79024 Human_SNP_ID_612961007 m1A Human chr16 + 86510561 86510561 86510561 AGAGCAGCGGCGGCAGCGGCGGCGGCGGCAGCAGCCACCCGATGTCTTCGGCGCCCGAGAAGCAG AGAGCAGCGGCGGCAGCGGCGGCGGCGGCAGCTGCCACCCGATGTCTTCGGCGCCCGAGAAGCAG A T FOXF1 Ensembl:ENSG00000103241 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:86510243..86510757 26863196 MeRIP-seq:(Medium) rs1431620507 Functional Loss SNV dbSNP153 33..33 33 - - - 79025 RMVar_ID_79025 Human_SNP_ID_612961471 m1A Human chr16 + 86511485 86511485 86511485 CCGCGGCCAACCCCCTGTCCGGCAGCCTCTCCACGCACTCCCTGGAGCAGCCGTATCTGCACCAG CCGCGGCCAACCCCCTGTCCGGCAGCCTCTCCTCGCACTCCCTGGAGCAGCCGTATCTGCACCAG A T FOXF1 Ensembl:ENSG00000103241 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:86511408..86511564 26863196 MeRIP-seq:(Medium) rs758858394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1747741 79026 RMVar_ID_79026 Human_SNP_ID_612981204 m1A Human chr16 + 86567517 86567517 86567517 GGGGATGGGCCGCTCCTACGCGCCCTACCACCACCACCAGCCCGCGGCGCCTAAGGACCTGGTGA GGGGATGGGCCGCTCCTACGCGCCCTACCACCCCCACCAGCCCGCGGCGCCTAAGGACCTGGTGA A C FOXC2 Ensembl:ENSG00000176692 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:86567466..86567671 26863196 MeRIP-seq:(Medium) rs1305839778 Functional Loss SNV dbSNP153 33..33 33 - - - 79027 RMVar_ID_79027 Human_SNP_ID_612981733 m1A Human chr16 + 86568516 86568513 86568516 CGCCACGGGCCACCACCACCAGCACCACGGCCACCACCACCCGCAGGCGCCGCCGCCCCCGCCGG CGCCACGGGCCACCACCACCAGCACCACGG___CCACCACCCGCAGGCGCCGCCGCCCCCGCCGG GCCA G FOXC2 Ensembl:ENSG00000176692 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86568202..86568598 26863196 MeRIP-seq:(Medium) rs1212412607 Functional Loss DEL dbSNP153 31..33 33 - - - 79028 RMVar_ID_79028 Human_SNP_ID_612981736 m1A Human chr16 + 86568522 86568522 86568522 GGGCCACCACCACCAGCACCACGGCCACCACCACCCGCAGGCGCCGCCGCCCCCGCCGGCTCCCC GGGCCACCACCACCAGCACCACGGCCACCACCCCCCGCAGGCGCCGCCGCCCCCGCCGGCTCCCC A C FOXC2 Ensembl:ENSG00000176692 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86568473..86568597 26863196 MeRIP-seq:(Medium) rs1035010170 Functional Loss SNV dbSNP153 33..33 33 - - - 79029 RMVar_ID_79029 Human_SNP_ID_612981755 m1A Human chr16 - 86568550 86568550 86568550 GCCCCGGGCTGCGGCGTCGGCTGGGGCTGGGGAGCCGGCGGGGGCGGCGGCGCCTGCGGGTGGTG GCCCCGGGCTGCGGCGTCGGCTGGGGCTGGGGGGCCGGCGGGGGCGGCGGCGCCTGCGGGTGGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:86568489..86568632 26863196 MeRIP-seq:(Medium) rs1000879434 Functional Loss SNV dbSNP153 33..33 33 - - - 79030 RMVar_ID_79030 Human_SNP_ID_612981797 m1A Human chr16 + 86568618 86568618 86568618 CGCGGCGCAGGCGGCCTCCTGGTATCTCAACCACAGCGGGGACCTGAACCACCTCCCCGGCCACA CGCGGCGCAGGCGGCCTCCTGGTATCTCAACCGCAGCGGGGACCTGAACCACCTCCCCGGCCACA A G FOXC2 Ensembl:ENSG00000176692 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:86568454..86568775 26863196 MeRIP-seq:(Medium) rs771161631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27446540 79031 RMVar_ID_79031 Human_SNP_ID_612982037 m1A Human chr16 + 86569086 86569086 86569086 CCCAGGAAACCCCTCCAAAGGGACGCAGCCCAACAAAATGAGTATTGATCTTAAAATCCCCCTCC CCCAGGAAACCCCTCCAAAGGGACGCAGCCCAGCAAAATGAGTATTGATCTTAAAATCCCCCTCC A G FOXC2 Ensembl:ENSG00000176692 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:86569033..86569134 26863196 MeRIP-seq:(Medium) rs190852335 Functional Loss SNV dbSNP153 33..33 33 - - - 79032 RMVar_ID_79032 Human_SNP_ID_612982038 m1A Human chr16 + 86569088 86569088 86569088 CAGGAAACCCCTCCAAAGGGACGCAGCCCAACAAAATGAGTATTGATCTTAAAATCCCCCTCCCC CAGGAAACCCCTCCAAAGGGACGCAGCCCAACGAAATGAGTATTGATCTTAAAATCCCCCTCCCC A G FOXC2 Ensembl:ENSG00000176692 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:86568976..86569150 26863196 MeRIP-seq:(Medium) rs939132468 Functional Loss SNV dbSNP153 33..33 33 - - - 79033 RMVar_ID_79033 Human_SNP_ID_612984363 m1A Human chr16 + 86576393 86576393 86576393 CCGGGACGGCGGGAGTTTCGGTAGAGGCAGGGATGTGCGTGCTGGACTTCGGGTGCCGCGTGGGG CCGGGACGGCGGGAGTTTCGGTAGAGGCAGGGGTGTGCGTGCTGGACTTCGGGTGCCGCGTGGGG A G FOXL1 Ensembl:ENSG00000176678 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86576357..86576618 26863196 MeRIP-seq:(Medium) rs1048941126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23705089 Human_Splice_Rec_1747933 79034 RMVar_ID_79034 Human_SNP_ID_612988315 m1A Human chr16 - 86587897 86587888 86587897 TGATGGTGATGATGATGGTGATAGTGATGGTGATGATGATGGTGGTGTTGATGGTGGAGGTGATG TGATGGTGATGATGATGGTGATAGTGATGGTG_________GTGGTGTTGATGGTGGAGGTGATG CCATCATCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86587851..86587951 26863196 MeRIP-seq:(Medium) rs1167522146 Functional Loss DEL dbSNP153 33..41 33 - - - 79035 RMVar_ID_79035 Human_SNP_ID_612988316 m1A Human chr16 - 86587897 86587888 86587897 TGATGGTGATGATGATGGTGATAGTGATGGTGATGATGATGGTGGTGTTGATGGTGGAGGTGATG TGATGGTGATGATGATGGTGATAGTGATGGTG___ATGATGGTGGTGTTGATGGTGGAGGTGATG CCATCATCAT CCATCAT - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86587851..86587951 26863196 MeRIP-seq:(Medium) rs1167522146 Functional Loss DEL dbSNP153 33..35 33 - - - 79036 RMVar_ID_79036 Human_SNP_ID_612988338 m1A Human chr16 + 86587938 86587918 86587939 CTATCACCATCATCATCACCATCACCATCATCACCATCACCACCACCATCACTATTAACATCATT CTATCACCATCAT_____________________CATCACCACCACCATCACTATTAACATCATT TCATCACCATCACCATCATCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86587873..86587953 26863196 MeRIP-seq:(Medium) rs1265381838 Functional Loss DEL dbSNP153 14..34 33 - - - 79037 RMVar_ID_79037 Human_SNP_ID_612988348 m1A Human chr16 + 86587938 86587933 86587939 CTATCACCATCATCATCACCATCACCATCATCACCATCACCACCACCATCACTATTAACATCATT CTATCACCATCATCATCACCATCACCAT______CATCACCACCACCATCACTATTAACATCATT TCATCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86587873..86587953 26863196 MeRIP-seq:(Medium) rs1163047021 Functional Loss DEL dbSNP153 29..34 33 - - - 79038 RMVar_ID_79038 Human_SNP_ID_613076587 m1A Human chr16 + 86845486 86845482 86845486 CCTGGTCTAGCCTCACACTCACCCCTGTGGTGAGTAAGGCCCTGCCTGGTCTAGCCTCACACTCA CCTGGTCTAGCCTCACACTCACCCCTGTG____GTAAGGCCCTGCCTGGTCTAGCCTCACACTCA GGTGA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:86845466..86845550 26863410 MeRIP-seq:(Medium) rs1287791573 Functional Loss DEL dbSNP153 30..33 33 - - - 79039 RMVar_ID_79039 Human_SNP_ID_613081664 m1A Human chr16 - 86861102 86861102 86861102 TCACCACCATCACCATCATCACCACCATCCTTATCATCACCATCATCACCATCACCACCATCACC TCACCACCATCACCATCATCACCACCATCCTTCTCATCACCATCATCACCATCACCACCATCACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86861043..86861161 26863196 MeRIP-seq:(Medium) rs939180351 Functional Loss SNV dbSNP153 33..33 33 - - - 79040 RMVar_ID_79040 Human_SNP_ID_613081776 m1A Human chr16 + 86861272 86861263 86861272 CAATGGTGGTAATGACGATGGTGGTGGTGATGATGGTGATGATGGTGGTGGTGATGATGGTGACG CAATGGTGGTAATGACGATGGTGG_________TGGTGATGATGGTGGTGGTGATGATGGTGACG GTGGTGATGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86861164..86861292 26863196 MeRIP-seq:(Medium) rs1378278439 Functional Loss DEL dbSNP153 25..33 33 - - - 79041 RMVar_ID_79041 Human_SNP_ID_613081780 m1A Human chr16 + 86861272 86861272 86861272 CAATGGTGGTAATGACGATGGTGGTGGTGATGATGGTGATGATGGTGGTGGTGATGATGGTGACG CAATGGTGGTAATGACGATGGTGGTGGTGATGGTGGTGATGATGGTGGTGGTGATGATGGTGACG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86861164..86861292 26863196 MeRIP-seq:(Medium) rs797000781 Functional Loss SNV dbSNP153 33..33 33 - - - 79042 RMVar_ID_79042 Human_SNP_ID_613087377 m1A Human chr16 + 86878055 86878051 86878055 ACTCTCTCATTCTCACTCTCACACACTCTCTCACTCTCTCACACTCACACACTCTCACACTCTCA ACTCTCTCATTCTCACTCTCACACACTCT____CTCTCTCACACTCACACACTCTCACACTCTCA TCTCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86877950..86878082 26863196 MeRIP-seq:(Medium) rs557052519 Functional Loss DEL dbSNP153 30..33 33 - - - 79043 RMVar_ID_79043 Human_SNP_ID_613087381 m1A Human chr16 + 86878055 86878055 86878055 ACTCTCTCATTCTCACTCTCACACACTCTCTCACTCTCTCACACTCACACACTCTCACACTCTCA ACTCTCTCATTCTCACTCTCACACACTCTCTCTCTCTCTCACACTCACACACTCTCACACTCTCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86877950..86878082 26863196 MeRIP-seq:(Medium) rs1298394824 Functional Loss SNV dbSNP153 33..33 33 - - - 79044 RMVar_ID_79044 Human_SNP_ID_613087394 m1A Human chr16 - 86878077 86878069 86878077 AGACAGAGTGTGTGAGAGTGTGTGAGAGTGTGAGAGTGTGTGAGTGTGAGAGAGTGAGAGAGTGT AGACAGAGTGTGTGAGAGTGTGTGAGAGTGTG________TGAGTGTGAGAGAGTGAGAGAGTGT ACACACTCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86877445..86878141 26863196 MeRIP-seq:(Medium) rs1181503499 Functional Loss DEL dbSNP153 33..40 33 - - - 79045 RMVar_ID_79045 Human_SNP_ID_613106045 m1A Human chr16 - 86932436 86932431 86932437 ACACTCACGGTCACACCTCACGCACATCTCACACTCATACATCTCACACTCAAGCTCACACTCAT ACACTCACGGTCACACCTCACGCACATCTCA______TACATCTCACACTCAAGCTCACACTCAT ATGAGTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86932134..86932578 26863196 MeRIP-seq:(Medium) rs938562439 Functional Loss DEL dbSNP153 32..37 33 - - - 79046 RMVar_ID_79046 Human_SNP_ID_613106050 m1A Human chr16 - 86932436 86932434 86932436 ACACTCACGGTCACACCTCACGCACATCTCACACTCATACATCTCACACTCAAGCTCACACTCAT ACACTCACGGTCACACCTCACGCACATCTCAC__TCATACATCTCACACTCAAGCTCACACTCAT AGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86932134..86932578 26863196 MeRIP-seq:(Medium) rs1347079346 Functional Loss DEL dbSNP153 33..34 33 - - - 79047 RMVar_ID_79047 Human_SNP_ID_613106054 m1A Human chr16 - 86932436 86932436 86932436 ACACTCACGGTCACACCTCACGCACATCTCACACTCATACATCTCACACTCAAGCTCACACTCAT ACACTCACGGTCACACCTCACGCACATCTCACTCTCATACATCTCACACTCAAGCTCACACTCAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86932134..86932578 26863196 MeRIP-seq:(Medium) rs1226925843 Functional Loss SNV dbSNP153 33..33 33 - - - 79048 RMVar_ID_79048 Human_SNP_ID_613106097 m1A Human chr16 + 86932511 86932508 86932511 TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGAAGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC TGTGAGGTGTGTGAATGTGAAGTGTGAGGT___GTGTGAGATGTGTGTGAGGTGTGACTGAGTGC TGAA T AC093519.2 Ensembl:ENSG00000287161 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86932460..86932578 26863196 MeRIP-seq:(Medium) rs1288067339 Functional Loss DEL dbSNP153 31..33 33 - - - 79049 RMVar_ID_79049 Human_SNP_ID_613106099 m1A Human chr16 + 86932511 86932509 86932511 TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGAAGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC TGTGAGGTGTGTGAATGTGAAGTGTGAGGTG__GTGTGAGATGTGTGTGAGGTGTGACTGAGTGC GAA G AC093519.2 Ensembl:ENSG00000287161 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86932460..86932578 26863196 MeRIP-seq:(Medium) rs1236187874 Functional Loss DEL dbSNP153 32..33 33 - - - 79050 RMVar_ID_79050 Human_SNP_ID_613106101 m1A Human chr16 + 86932511 86932511 86932511 TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGAAGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGAGGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC A G AC093519.2 Ensembl:ENSG00000287161 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86932460..86932578 26863196 MeRIP-seq:(Medium) rs574912947 Functional Loss SNV dbSNP153 33..33 33 - - - 79051 RMVar_ID_79051 Human_SNP_ID_613106102 m1A Human chr16 + 86932511 86932511 86932511 TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGAAGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC TGTGAGGTGTGTGAATGTGAAGTGTGAGGTGATGTGTGAGATGTGTGTGAGGTGTGACTGAGTGC A T AC093519.2 Ensembl:ENSG00000287161 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:86932460..86932578 26863196 MeRIP-seq:(Medium) rs574912947 Functional Loss SNV dbSNP153 33..33 33 - - - 79052 RMVar_ID_79052 Human_SNP_ID_613204252 m1A Human chr16 + 87209943 87209937 87209943 TGATGATAGTGATGGTGATGATGATGGTGGTGATGGTGATGGTGCTGATGGTGGTGATGATAGTG TGATGATAGTGATGGTGATGATGATGG______TGGTGATGGTGCTGATGGTGGTGATGATAGTG GTGGTGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:87209870..87209984 26863196 MeRIP-seq:(Medium) rs1239536754 Functional Loss DEL dbSNP153 28..33 33 - - - 79053 RMVar_ID_79053 Human_SNP_ID_613204414 m1A Human chr16 + 87210273 87210273 87210273 TGATGCTGATGGTGGTGATGATGCTGGTGATGATGGTGATGGTGATAATGGTGATGGTGATAATG TGATGCTGATGGTGGTGATGATGCTGGTGATGCTGGTGATGGTGATAATGGTGATGGTGATAATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:87210240..87210344;chr16:87210231..87210350 26863196 MeRIP-seq:(Medium) rs1358978545 Functional Loss SNV dbSNP153 33..33 33 - - - 79054 RMVar_ID_79054 Human_SNP_ID_613204434 m1A Human chr16 - 87210304 87210304 87210304 TCACCATCATCATCATCACCATCACCATCACCATTATCACCATCACCATTATCACCATCACCATC TCACCATCATCATCATCACCATCACCATCACCGTTATCACCATCACCATTATCACCATCACCATC T C C16orf95 Ensembl:ENSG00000260456 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:87210255..87210354 26863196 MeRIP-seq:(Medium) rs930609277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_198208,Human_RBP_ID_261687 79055 RMVar_ID_79055 Human_SNP_ID_613240154 m1A Human chr16 + 87317341 87317341 87317341 CCGCCTTTCCCTCCTGCCCCAGGAGGAACCCAACCCGAGCTCAACCCCAGCCCCAACCTCAACCG CCGCCTTTCCCTCCTGCCCCAGGAGGAACCCAGCCCGAGCTCAACCCCAGCCCCAACCTCAACCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87317125..87317380 26863196 MeRIP-seq:(Medium) rs1293791132 Functional Loss SNV dbSNP153 33..33 33 - - - 79056 RMVar_ID_79056 Human_SNP_ID_613262761 m1A Human chr16 + 87384054 87384054 87384054 TGCCCCGTGTGAGGCTCGAACTCACGACCTTCAGATTATGAGACTGACGCGCTGCCTACTGCGCT TGCCCCGTGTGAGGCTCGAACTCACGACCTTCCGATTATGAGACTGACGCGCTGCCTACTGCGCT A C MAP1LC3B Ensembl:ENSG00000140941 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87383913..87384189 26863196 MeRIP-seq:(Medium) rs973213570 Functional Loss SNV dbSNP153 33..33 33 - - - 79057 RMVar_ID_79057 Human_SNP_ID_613265656 m1A Human chr16 + 87392375 87392365 87392375 GATTCGCCGCCGCAGCAGCCGCCGCCCCCGGGAGCCGCCGGGACCCTCGCGTCGTCGCCGCCGCC GATTCGCCGCCGCAGCAGCCGCC__________GCCGCCGGGACCCTCGCGTCGTCGCCGCCGCC CGCCCCCGGGA C MAP1LC3B Ensembl:ENSG00000140941 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87392301..87392604;chr16:87392326..87392554;chr16:87392326..87392727;chr16:87392301..87392733;chr16:87392298..87392798 26863196 MeRIP-seq:(Medium) rs1567497156 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_233736,Human_RBP_ID_761433,Human_RBP_ID_818776,Human_RBP_ID_4387928,Human_RBP_ID_9325311,Human_RBP_ID_9374781,Human_RBP_ID_17371545,Human_RBP_ID_17669531,Human_RBP_ID_22532718,Human_RBP_ID_26329304 Human_Splice_Rec_1748171,Human_Splice_Rec_1748177,Human_Splice_Rec_1748185,Human_Splice_Rec_1748189,Human_Splice_Rec_1748203 RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 79058 RMVar_ID_79058 Human_SNP_ID_613265754 m1A Human chr16 + 87392425 87392425 87392425 GTCGTCGCCGCCGCCGCCGCCCAGATCCCTGCACCATGCCGTCGGAGAAGACCTTCAAGCAGCGC GTCGTCGCCGCCGCCGCCGCCCAGATCCCTGCGCCATGCCGTCGGAGAAGACCTTCAAGCAGCGC A G MAP1LC3B Ensembl:ENSG00000140941 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87392326..87392498 26863410 MeRIP-seq:(Medium) rs1417919745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233736,Human_RBP_ID_761434,Human_RBP_ID_4394065,Human_RBP_ID_9325311,Human_RBP_ID_9374782,Human_RBP_ID_17371546,Human_RBP_ID_17669531,Human_RBP_ID_23114120,Human_RBP_ID_26329304,Human_RBP_ID_26447029 Human_Splice_Rec_1748171,Human_Splice_Rec_1748177,Human_Splice_Rec_1748185,Human_Splice_Rec_1748189,Human_Splice_Rec_1748203 Human_miRNA_ID_2493725 RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 79059 RMVar_ID_79059 Human_SNP_ID_613265775 m1A Human chr16 + 87392438 87392438 87392438 CCGCCGCCCAGATCCCTGCACCATGCCGTCGGAGAAGACCTTCAAGCAGCGCCGCACCTTCGGTG CCGCCGCCCAGATCCCTGCACCATGCCGTCGGTGAAGACCTTCAAGCAGCGCCGCACCTTCGGTG A T MAP1LC3B Ensembl:ENSG00000140941 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:87392388..87392505 32194978 MeRIP-seq:(Medium) rs1355405976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233736,Human_RBP_ID_277763,Human_RBP_ID_4394066,Human_RBP_ID_9325311,Human_RBP_ID_9374782,Human_RBP_ID_17371546,Human_RBP_ID_17669531,Human_RBP_ID_18686108,Human_RBP_ID_23114120,Human_RBP_ID_26329304 Human_Splice_Rec_1748171,Human_Splice_Rec_1748177,Human_Splice_Rec_1748185,Human_Splice_Rec_1748189,Human_Splice_Rec_1748203 Human_miRNA_ID_2728167 RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 79060 RMVar_ID_79060 Human_SNP_ID_613265784 m1A Human chr16 - 87392447 87392447 87392447 GGCGACACTCACCGAAGGTGCGGCGCTGCTTGAAGGTCTTCTCCGACGGCATGGTGCAGGGATCT GGCGACACTCACCGAAGGTGCGGCGCTGCTTGTAGGTCTTCTCCGACGGCATGGTGCAGGGATCT T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:87392347..87392498 26863410 MeRIP-seq:(Medium) rs1367485018 Functional Loss SNV dbSNP153 33..33 33 - - - 79061 RMVar_ID_79061 Human_SNP_ID_613265785 m1A Human chr16 - 87392447 87392447 87392447 GGCGACACTCACCGAAGGTGCGGCGCTGCTTGAAGGTCTTCTCCGACGGCATGGTGCAGGGATCT GGCGACACTCACCGAAGGTGCGGCGCTGCTTGGAGGTCTTCTCCGACGGCATGGTGCAGGGATCT T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:87392347..87392498 26863410 MeRIP-seq:(Medium) rs1367485018 Functional Loss SNV dbSNP153 33..33 33 - - - 79062 RMVar_ID_79062 Human_SNP_ID_613272555 m1A Human chr16 - 87411801 87411801 87411801 CCTTCAGTCCCATGTGCAGCAGCGGCTACGTCAGCGCCCAGCAGTACGGCGGCGGCTCCACCTTC CCTTCAGTCCCATGTGCAGCAGCGGCTACGTCGGCGCCCAGCAGTACGGCGGCGGCTCCACCTTC T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:87411751..87411975 26863196 MeRIP-seq:(Medium) rs747016017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17488326,Human_RBP_ID_18940732,Human_RBP_ID_27247675 RMVar_hsa_circ_16065,RMVar_hsa_circ_124445,RMVar_hsa_circ_180411,RMVar_hsa_circ_180412,RMVar_hsa_circ_91262,RMVar_hsa_circ_268130 79063 RMVar_ID_79063 Human_SNP_ID_613272562 m1A Human chr16 - 87411816 87411816 87411816 CCTTCCCCTTCTTGCCCTTCAGTCCCATGTGCAGCAGCGGCTACGTCAGCGCCCAGCAGTACGGC CCTTCCCCTTCTTGCCCTTCAGTCCCATGTGCGGCAGCGGCTACGTCAGCGCCCAGCAGTACGGC T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87411765..87411949 26863196 MeRIP-seq:(Medium) rs1362887973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5142562,Human_RBP_ID_17488326,Human_RBP_ID_18940732,Human_RBP_ID_22206785,Human_RBP_ID_27247675 RMVar_hsa_circ_16065,RMVar_hsa_circ_124445,RMVar_hsa_circ_180411,RMVar_hsa_circ_180412,RMVar_hsa_circ_91262,RMVar_hsa_circ_268130 79064 RMVar_ID_79064 Human_SNP_ID_613272607 m1A Human chr16 - 87411878 87411878 87411878 TGGCCTGACTGTCAGCTACGCCAACTACTTCCAGCACCCGTTCTCCGGTCCGTCCGTGTTCACCT TGGCCTGACTGTCAGCTACGCCAACTACTTCCCGCACCCGTTCTCCGGTCCGTCCGTGTTCACCT T G ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87411701..87412145 26863196 MeRIP-seq:(Medium) rs1387614657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18940732,Human_RBP_ID_27446669 Human_miRNA_ID_172052 RMVar_hsa_circ_16065,RMVar_hsa_circ_124445,RMVar_hsa_circ_180411,RMVar_hsa_circ_180412,RMVar_hsa_circ_91262,RMVar_hsa_circ_268130 79065 RMVar_ID_79065 Human_SNP_ID_613272620 m1A Human chr16 + 87411901 87411901 87411901 AACGGGTGCTGGAAGTAGTTGGCGTAGCTGACAGTCAGGCCACTCGAGCCGCAGCTGCCGCTGCA AACGGGTGCTGGAAGTAGTTGGCGTAGCTGACGGTCAGGCCACTCGAGCCGCAGCTGCCGCTGCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:87411724..87412000 26863196 MeRIP-seq:(Medium) rs1266368102 Functional Loss SNV dbSNP153 33..33 33 - - - 79066 RMVar_ID_79066 Human_SNP_ID_613289526 m1A Human chr16 - 87460131 87460131 87460131 AAAATAAGATGATTCTGTTTCTGTTCCCTCAGATCACTCCAAGAACTGAGGCCCCTGTCAGCAGT AAAATAAGATGATTCTGTTTCTGTTCCCTCAGGTCACTCCAAGAACTGAGGCCCCTGTCAGCAGT T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87460112..87460184 26863196 MeRIP-seq:(Medium) rs11648852 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_892740,Human_RBP_ID_4388177,Human_RBP_ID_18288196,Human_RBP_ID_18686177,Human_RBP_ID_25235365 Human_Splice_Rec_1748208,Human_Splice_Rec_1748232,Human_Splice_Rec_1748256 Human_miRNA_ID_2615960 GWAS_ID_9512,GWAS_ID_9513,GWAS_ID_9514,GWAS_ID_9515,GWAS_ID_9516,GWAS_ID_9517 RMVar_hsa_circ_80504,RMVar_hsa_circ_180417,RMVar_hsa_circ_122649,RMVar_hsa_circ_180422,RMVar_hsa_circ_316239,RMVar_hsa_circ_180418,RMVar_hsa_circ_180427,RMVar_hsa_circ_180424,RMVar_hsa_circ_75879,RMVar_hsa_circ_180425,RMVar_hsa_circ_361034,RMVar_hsa_circ_328542,RMVar_hsa_circ_180426 79067 RMVar_ID_79067 Human_SNP_ID_613295418 m1A Human chr16 - 87477744 87477744 87477744 GGGGATGCGGTGGGGGCGTGGCGGTGTTCCCCAGGTGCAGGAGGCTGCTCTGAGGGTGTCGCATG GGGGATGCGGTGGGGGCGTGGCGGTGTTCCCCGGGTGCAGGAGGCTGCTCTGAGGGTGTCGCATG T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87477741..87477997 26863196 MeRIP-seq:(Medium) rs1408584862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21971563,Human_RBP_ID_22474258,Human_RBP_ID_23705364 79068 RMVar_ID_79068 Human_SNP_ID_613300018 m1A Human chr16 - 87491730 87491730 87491730 GATCCAGAGCAGCCTGAACGGCGGCGGGGGCCACGGCGGCAAGGGCGCGCCCGGGCCGGGCGGCG GATCCAGAGCAGCCTGAACGGCGGCGGGGGCCGCGGCGGCAAGGGCGCGCCCGGGCCGGGCGGCG T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87491663..87491821 26863196 MeRIP-seq:(Medium) rs755854900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234904,Human_RBP_ID_4404345,Human_RBP_ID_9374787,Human_RBP_ID_22053526 Human_Splice_Rec_1748207,Human_Splice_Rec_1748231,Human_Splice_Rec_1748255 79069 RMVar_ID_79069 Human_SNP_ID_613300433 m1A Human chr16 + 87492685 87492685 87492685 CCGCAGGGTCTGTCACTGCGGGCCGCCCCCCGACGGAGCCGCCCCGGCCATGCCGTCGCCGCCGC CCGCAGGGTCTGTCACTGCGGGCCGCCCCCCGTCGGAGCCGCCCCGGCCATGCCGTCGCCGCCGC A T AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:87492391..87493000 26863196 MeRIP-seq:(Medium) rs912383996 Functional Loss SNV dbSNP153 33..33 33 - - - 79070 RMVar_ID_79070 Human_SNP_ID_613300565 m1A Human chr16 + 87492935 87492908 87492935 CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGACGGCGACGGCGACGGCGGAGGAGGCGCCGGCC CGAGCG___________________________CGGCGACGGCGACGGCGGAGGAGGCGCCGGCC GCGGCGGCGGCGGCGACGGCGACGGCGA G AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87492835..87492953 26863410 MeRIP-seq:(Medium) rs1313913806 Functional Loss DEL dbSNP153 7..33 33 - - - 79071 RMVar_ID_79071 Human_SNP_ID_613300576 m1A Human chr16 + 87492935 87492911 87492935 CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGACGGCGACGGCGACGGCGGAGGAGGCGCCGGCC CGAGCGCGG________________________CGGCGACGGCGACGGCGGAGGAGGCGCCGGCC GCGGCGGCGGCGACGGCGACGGCGA G AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87492835..87492953 26863410 MeRIP-seq:(Medium) rs1555526995 Functional Loss DEL dbSNP153 10..33 33 - - - 79072 RMVar_ID_79072 Human_SNP_ID_613300628 m1A Human chr16 + 87492935 87492925 87492935 CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGACGGCGACGGCGACGGCGGAGGAGGCGCCGGCC CGAGCGCGGCGGCGGCGGCGACG__________CGGCGACGGCGACGGCGGAGGAGGCGCCGGCC GGCGACGGCGA G AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87492835..87492953 26863410 MeRIP-seq:(Medium) rs1567549629 Functional Loss DEL dbSNP153 24..33 33 - - - 79073 RMVar_ID_79073 Human_SNP_ID_613300644 m1A Human chr16 + 87492935 87492935 87492935 CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGACGGCGACGGCGACGGCGGAGGAGGCGCCGGCC CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGCCGGCGACGGCGACGGCGGAGGAGGCGCCGGCC A C AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87492835..87492953 26863410 MeRIP-seq:(Medium) rs1190418687 Functional Loss SNV dbSNP153 33..33 33 - - - 79074 RMVar_ID_79074 Human_SNP_ID_613300645 m1A Human chr16 + 87492935 87492935 87492935 CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGACGGCGACGGCGACGGCGGAGGAGGCGCCGGCC CGAGCGCGGCGGCGGCGGCGACGGCGACGGCGGCGGCGACGGCGACGGCGGAGGAGGCGCCGGCC A G AC092720.3 Ensembl:ENSG00000288568 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87492835..87492953 26863410 MeRIP-seq:(Medium) rs1190418687 Functional Loss SNV dbSNP153 33..33 33 - - - 79075 RMVar_ID_79075 Human_SNP_ID_613335563 m1A Human chr16 + 87602548 87602534 87602549 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCA_______________CGCCGCCGCCGCCGCCCGAGCCGCCGCATTG ACGCCGCCGCCGCCAC A JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1317890194 Functional Loss DEL dbSNP153 20..34 33 - - - 79076 RMVar_ID_79076 Human_SNP_ID_613335566 m1A Human chr16 + 87602548 87602536 87602548 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCACG____________CCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GCCGCCGCCGCCA G JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1283912589 Functional Loss DEL dbSNP153 22..33 33 - - - 79077 RMVar_ID_79077 Human_SNP_ID_613335570 m1A Human chr16 + 87602548 87602539 87602548 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCACGCCG_________CCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GCCGCCGCCA G JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1401024015 Functional Loss DEL dbSNP153 25..33 33 - - - 79078 RMVar_ID_79078 Human_SNP_ID_613335580 m1A Human chr16 + 87602548 87602545 87602548 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCACGCCGCCGCCG___CCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GCCA G JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1172249015 Functional Loss DEL dbSNP153 31..33 33 - - - 79079 RMVar_ID_79079 Human_SNP_ID_613335589 m1A Human chr16 + 87602548 87602548 87602548 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCCCCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG A C JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1381683679 Functional Loss SNV dbSNP153 33..33 33 - - - 79080 RMVar_ID_79080 Human_SNP_ID_613335590 m1A Human chr16 + 87602548 87602548 87602548 GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG GAGCCGGGCCCGGAGCGCACGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGAGCCGCCGCATTG A G JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:87602426..87602642 26863196 MeRIP-seq:(Medium) rs1381683679 Functional Loss SNV dbSNP153 33..33 33 - - - 79081 RMVar_ID_79081 Human_SNP_ID_613335598 m1A Human chr16 + 87602568 87602556 87602568 GCCGCCGCCGCCACCGCCGCCGCCGCCGCCCGAGCCGCCGCATTGCTGCTGCTGCTGCCGCCGCC GCCGCCGCCGCCACCGCCGCC____________GCCGCCGCATTGCTGCTGCTGCTGCCGCCGCC CGCCGCCGCCCGA C JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87602552..87602651 26863196 MeRIP-seq:(Medium) rs1239488799 Functional Loss DEL dbSNP153 22..33 33 - - - 79082 RMVar_ID_79082 Human_SNP_ID_613335714 m1A Human chr16 - 87602820 87602820 87602820 GCAGGAGCGGCGGCGGCGGGGCCCGCGGCTCCACCTCAGCGGCGAGAGGGCCCCTCGCCGGCAGC GCAGGAGCGGCGGCGGCGGGGCCCGCGGCTCCCCCTCAGCGGCGAGAGGGCCCCTCGCCGGCAGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87602726..87602850 26863410 MeRIP-seq:(Medium) rs945270429 Functional Loss SNV dbSNP153 33..33 33 - - - 79083 RMVar_ID_79083 Human_SNP_ID_613335728 m1A Human chr16 - 87602857 87602853 87602857 ACCGGAGGGGAGGGGGAGGGGAGGAGGGAGGGAGGGGGCAGGAGCGGCGGCGGCGGGGCCCGCGG ACCGGAGGGGAGGGGGAGGGGAGGAGGGAGGG____GGCAGGAGCGGCGGCGGCGGGGCCCGCGG CCCCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:87602809..87602934 32194978 MeRIP-seq:(Medium) rs993802029 Functional Loss DEL dbSNP153 33..36 33 - - - 79084 RMVar_ID_79084 Human_SNP_ID_613335732 m1A Human chr16 - 87602857 87602857 87602857 ACCGGAGGGGAGGGGGAGGGGAGGAGGGAGGGAGGGGGCAGGAGCGGCGGCGGCGGGGCCCGCGG ACCGGAGGGGAGGGGGAGGGGAGGAGGGAGGGGGGGGGCAGGAGCGGCGGCGGCGGGGCCCGCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:87602809..87602934 32194978 MeRIP-seq:(Medium) rs1046357169 Functional Loss SNV dbSNP153 33..33 33 - - - 79085 RMVar_ID_79085 Human_SNP_ID_613351445 m1A Human chr16 + 87644230 87644230 87644230 GCCAGGCTGTGCCCCCTCCTCTGTCGCTGGGCACTCACCCCTCTCTCATTTTCTCCCCAGGGACC GCCAGGCTGTGCCCCCTCCTCTGTCGCTGGGCGCTCACCCCTCTCTCATTTTCTCCCCAGGGACC A G JPH3 Ensembl:ENSG00000154118 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87644227..87644351 26863196 MeRIP-seq:(Medium) rs376915648 Functional Loss SNV dbSNP153 33..33 33 - - - 79086 RMVar_ID_79086 Human_SNP_ID_613351479 m1A Human chr16 - 87644283 87644283 87644283 CTCTGCCGGACGCCGTAGCCCTGGCGCATGCCACCGACCCACTGGCCCTGGTAGGTCCCTGGGGA CTCTGCCGGACGCCGTAGCCCTGGCGCATGCCCCCGACCCACTGGCCCTGGTAGGTCCCTGGGGA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:87644253..87644385 26863196 MeRIP-seq:(Medium) rs780771696 Functional Loss SNV dbSNP153 33..33 33 - - - 79087 RMVar_ID_79087 Human_SNP_ID_613375661 m1A Human chr16 - 87700361 87700361 87700361 TACTGCAGGAGGGCGGCATCATGATGTCCTGAAGCTTGTTGCGCCCGGTGCTGTCGGCCGGCTGA TACTGCAGGAGGGCGGCATCATGATGTCCTGACGCTTGTTGCGCCCGGTGCTGTCGGCCGGCTGA T G KLHDC4 Ensembl:ENSG00000104731 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87700310..87700420 26863196 MeRIP-seq:(Medium) rs1037282880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234786,Human_RBP_ID_1179576,Human_RBP_ID_12838086,Human_RBP_ID_17564806,Human_RBP_ID_22712329 79088 RMVar_ID_79088 Human_SNP_ID_613376354 m1A Human chr16 - 87701658 87701658 87701658 AGGATGTTTATCCCAAATGCCAGGAGTGGACGAGGCGGACGAGTGGCAGTGAGGTAGGCATGTGA AGGATGTTTATCCCAAATGCCAGGAGTGGACGTGGCGGACGAGTGGCAGTGAGGTAGGCATGTGA T A KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87701608..87701833 26863196 MeRIP-seq:(Medium) rs770864132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763190,Human_RBP_ID_1524090,Human_RBP_ID_3507723,Human_RBP_ID_12838122,Human_RBP_ID_18190585,Human_RBP_ID_18939549,Human_RBP_ID_22714672,Human_RBP_ID_23705457,Human_RBP_ID_27572589 Human_Splice_Rec_1748379 79089 RMVar_ID_79089 Human_SNP_ID_613376357 m1A Human chr16 - 87701661 87701661 87701661 GACAGGATGTTTATCCCAAATGCCAGGAGTGGACGAGGCGGACGAGTGGCAGTGAGGTAGGCATG GACAGGATGTTTATCCCAAATGCCAGGAGTGGTCGAGGCGGACGAGTGGCAGTGAGGTAGGCATG T A KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87701580..87701906 26863196 MeRIP-seq:(Medium) rs1567628275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763190,Human_RBP_ID_3507723,Human_RBP_ID_12838124,Human_RBP_ID_18190585,Human_RBP_ID_18939549,Human_RBP_ID_22714672,Human_RBP_ID_23705457,Human_RBP_ID_27572589 Human_Splice_Rec_1748379 79090 RMVar_ID_79090 Human_SNP_ID_613379520 m1A Human chr16 - 87708388 87708388 87708388 GGAGGTTGAGGGCGCCGAGGGTGGGGTCGACGACGAAGACAGCGGAGAGGAGAGCGGTGCGGAGG GGAGGTTGAGGGCGCCGAGGGTGGGGTCGACGGCGAAGACAGCGGAGAGGAGAGCGGTGCGGAGG T C KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87707951..87709421 26863196 MeRIP-seq:(Medium) rs780128533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44551,Human_RBP_ID_233555,Human_RBP_ID_892743,Human_RBP_ID_3949651,Human_RBP_ID_4388376,Human_RBP_ID_5114000,Human_RBP_ID_9373311,Human_RBP_ID_18987095,Human_RBP_ID_19075369,Human_RBP_ID_20169188,Human_RBP_ID_22583096,Human_RBP_ID_22712343,Human_RBP_ID_22944709,Human_RBP_ID_23118501,Human_RBP_ID_24544550,Human_RBP_ID_26329307,Human_RBP_ID_26780738 Human_Splice_Rec_1748370,Human_Splice_Rec_1748371,Human_Splice_Rec_1748381,Human_Splice_Rec_1748396,Human_Splice_Rec_1748397,Human_Splice_Rec_1748414,Human_Splice_Rec_1748415,Human_Splice_Rec_1748434,Human_Splice_Rec_1748435,Human_Splice_Rec_1748456,Human_Splice_Rec_1748457,Human_Splice_Rec_1748470,Human_Splice_Rec_1748471,Human_Splice_Rec_1748475,Human_Splice_Rec_1748494,Human_Splice_Rec_1748495,Human_Splice_Rec_1748514,Human_Splice_Rec_1748515 RMVar_hsa_circ_95917,RMVar_hsa_circ_300861,RMVar_hsa_circ_63705,RMVar_hsa_circ_65390,RMVar_hsa_circ_15052,RMVar_hsa_circ_180431 79091 RMVar_ID_79091 Human_SNP_ID_613379528 m1A Human chr16 + 87708394 87708394 87708394 CACCGCTCTCCTCTCCGCTGTCTTCGTCGTCGACCCCACCCTCGGCGCCCTCAACCTCCTCACTG CACCGCTCTCCTCTCCGCTGTCTTCGTCGTCGGCCCCACCCTCGGCGCCCTCAACCTCCTCACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87707949..87709696;chr16:87707939..87709677;chr16:87707968..87709677 26863196 MeRIP-seq:(Medium) rs1019588666 Functional Loss SNV dbSNP153 33..33 33 - - - 79092 RMVar_ID_79092 Human_SNP_ID_613380137 m1A Human chr16 + 87709593 87709593 87709593 AGCTGCACAGGCCCCTGGGTGCCAGCTCCCCCACACGCCGGCCTGCTACCACCTTCGGGCTCCTC AGCTGCACAGGCCCCTGGGTGCCAGCTCCCCCCCACGCCGGCCTGCTACCACCTTCGGGCTCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87709489..87709675 26863196 MeRIP-seq:(Medium) rs772927197 Functional Loss SNV dbSNP153 33..33 33 - - - 79093 RMVar_ID_79093 Human_SNP_ID_613380138 m1A Human chr16 + 87709593 87709593 87709593 AGCTGCACAGGCCCCTGGGTGCCAGCTCCCCCACACGCCGGCCTGCTACCACCTTCGGGCTCCTC AGCTGCACAGGCCCCTGGGTGCCAGCTCCCCCGCACGCCGGCCTGCTACCACCTTCGGGCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87709489..87709675 26863196 MeRIP-seq:(Medium) rs772927197 Functional Loss SNV dbSNP153 33..33 33 - - - 79094 RMVar_ID_79094 Human_SNP_ID_613380782 m1A Human chr16 - 87711197 87711197 87711197 GCAACCTCTGAGTAGCATGCGCCGTGGTGCGCAGCCCTAACTTGGGTCCCTGCCACCACTGCCTT GCAACCTCTGAGTAGCATGCGCCGTGGTGCGCGGCCCTAACTTGGGTCCCTGCCACCACTGCCTT T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87711192..87711317 26863196 MeRIP-seq:(Medium) rs1370491877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892746,Human_RBP_ID_1524151,Human_RBP_ID_18686334,Human_RBP_ID_19072277 RMVar_hsa_circ_8657,RMVar_hsa_circ_95917,RMVar_hsa_circ_300861,RMVar_hsa_circ_63705,RMVar_hsa_circ_112074,RMVar_hsa_circ_15052,RMVar_hsa_circ_180431,RMVar_hsa_circ_92030,RMVar_hsa_circ_180432,RMVar_hsa_circ_180433 79095 RMVar_ID_79095 Human_SNP_ID_613382104 m1A Human chr16 + 87714303 87714302 87714303 CAGTCAGTCCATCATCAATGCCCCCAAAGGTGATTGCCCAGCAGACACCAGGGCTATGGAGCCTG CAGTCAGTCCATCATCAATGCCCCCAAAGGTG_TTGCCCAGCAGACACCAGGGCTATGGAGCCTG GA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:87714280..87714412 26863196 MeRIP-seq:(Medium) rs1197058471 Functional Loss DEL dbSNP153 33..33 33 - - - 79096 RMVar_ID_79096 Human_SNP_ID_613387441 m1A Human chr16 + 87726679 87726679 87726679 GTCTCCCCACGCCGCGCCTCGCCCGTCTCCCCACCCCGCGCCTCGCCCGTCTCCCCACCCCGCGC GTCTCCCCACGCCGCGCCTCGCCCGTCTCCCCCCCCCGCGCCTCGCCCGTCTCCCCACCCCGCGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87726675..87726777;chr16:87726659..87726771 26863196 MeRIP-seq:(Medium) rs1180600562 Functional Loss SNV dbSNP153 33..33 33 - - - 79097 RMVar_ID_79097 Human_SNP_ID_613387442 m1A Human chr16 + 87726679 87726679 87726679 GTCTCCCCACGCCGCGCCTCGCCCGTCTCCCCACCCCGCGCCTCGCCCGTCTCCCCACCCCGCGC GTCTCCCCACGCCGCGCCTCGCCCGTCTCCCCGCCCCGCGCCTCGCCCGTCTCCCCACCCCGCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87726675..87726777;chr16:87726659..87726771 26863196 MeRIP-seq:(Medium) rs1180600562 Functional Loss SNV dbSNP153 33..33 33 - - - 79098 RMVar_ID_79098 Human_SNP_ID_613390526 m1A Human chr16 - 87733744 87733642 87733744 GGATCCCAGGGAGTGGATTCCTAAGTAGGAGGAGAGGCAGGTCATCAGTGAGGATCCCAGGGAGT GGATCCCAGGGAGTGGATTCCTAAGTAGGAGG_________________________________ GCCTCCTACTTAGGAATCCACTCCCTGGGATCCTCACTGATGACCTGCCTCGCCTCCTACTTAGGAATCCACTCCCTGGGATCCTCACTGATGACCTGCCTCT G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87733699..87733902 26863196 MeRIP-seq:(Medium) rs1567739438 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_12838808,Human_RBP_ID_21973272,Human_RBP_ID_22474873 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79099 RMVar_ID_79099 Human_SNP_ID_613390553 m1A Human chr16 - 87733744 87733742 87733745 GGATCCCAGGGAGTGGATTCCTAAGTAGGAGGAGAGGCAGGTCATCAGTGAGGATCCCAGGGAGT GGATCCCAGGGAGTGGATTCCTAAGTAGGAG___AGGCAGGTCATCAGTGAGGATCCCAGGGAGT TCTC T KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87733699..87733902 26863196 MeRIP-seq:(Medium) rs1180134906 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12838808,Human_RBP_ID_21973272,Human_RBP_ID_22474873 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79100 RMVar_ID_79100 Human_SNP_ID_613390554 m1A Human chr16 - 87733744 87733744 87733744 GGATCCCAGGGAGTGGATTCCTAAGTAGGAGGAGAGGCAGGTCATCAGTGAGGATCCCAGGGAGT GGATCCCAGGGAGTGGATTCCTAAGTAGGAGGCGAGGCAGGTCATCAGTGAGGATCCCAGGGAGT T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87733699..87733902 26863196 MeRIP-seq:(Medium) rs12446142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12838808,Human_RBP_ID_21973272,Human_RBP_ID_22474873 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79101 RMVar_ID_79101 Human_SNP_ID_613390556 m1A Human chr16 - 87733747 87733747 87733747 TGAGGATCCCAGGGAGTGGATTCCTAAGTAGGAGGAGAGGCAGGTCATCAGTGAGGATCCCAGGG TGAGGATCCCAGGGAGTGGATTCCTAAGTAGGCGGAGAGGCAGGTCATCAGTGAGGATCCCAGGG T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87733684..87733865;chr16:87733688..87733950 26863196 MeRIP-seq:(Medium) rs1037616871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12838808,Human_RBP_ID_21973272,Human_RBP_ID_22474873 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79102 RMVar_ID_79102 Human_SNP_ID_613392748 m1A Human chr16 - 87738595 87738590 87738595 TGTGGATGGATGAGGTGCTGTGTGGATGGATGAGGTGCTGGTGTGTGGATGGATGAGGTGCTGGT TGTGGATGGATGAGGTGCTGTGTGGATGGATG_____CTGGTGTGTGGATGGATGAGGTGCTGGT GCACCT G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87738576..87738647 26863196 MeRIP-seq:(Medium) rs201303083 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3503021,Human_RBP_ID_5647102,Human_RBP_ID_8441288,Human_RBP_ID_17256197,Human_RBP_ID_23705600 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79103 RMVar_ID_79103 Human_SNP_ID_613392753 m1A Human chr16 - 87738595 87738595 87738595 TGTGGATGGATGAGGTGCTGTGTGGATGGATGAGGTGCTGGTGTGTGGATGGATGAGGTGCTGGT TGTGGATGGATGAGGTGCTGTGTGGATGGATGTGGTGCTGGTGTGTGGATGGATGAGGTGCTGGT T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87738576..87738647 26863196 MeRIP-seq:(Medium) rs1201731521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503021,Human_RBP_ID_5647102,Human_RBP_ID_8441288,Human_RBP_ID_17256197,Human_RBP_ID_23705600 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79104 RMVar_ID_79104 Human_SNP_ID_613392754 m1A Human chr16 - 87738618 87738595 87738619 TGTGGATGGATGAGATGCTGGTGTGTGGATGGATGAGGTGCTGTGTGGATGGATGAGGTGCTGGT TGTGGATGGATGAGATGCTGGTGTGTGGATG________________________AGGTGCTGGT TCATCCATCCACACAGCACCTCATC T KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87738447..87738670 26863196 MeRIP-seq:(Medium) rs1297785179 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_3503021,Human_RBP_ID_5647102,Human_RBP_ID_17256197,Human_RBP_ID_23705600,Human_RBP_ID_27837925 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79105 RMVar_ID_79105 Human_SNP_ID_613392766 m1A Human chr16 - 87738618 87738615 87738619 TGTGGATGGATGAGATGCTGGTGTGTGGATGGATGAGGTGCTGTGTGGATGGATGAGGTGCTGGT TGTGGATGGATGAGATGCTGGTGTGTGGATG____AGGTGCTGTGTGGATGGATGAGGTGCTGGT TCATC T KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87738447..87738670 26863196 MeRIP-seq:(Medium) rs1312962268 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3503021,Human_RBP_ID_5647102,Human_RBP_ID_17256197,Human_RBP_ID_23705600,Human_RBP_ID_27837925 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79106 RMVar_ID_79106 Human_SNP_ID_613392768 m1A Human chr16 - 87738618 87738618 87738618 TGTGGATGGATGAGATGCTGGTGTGTGGATGGATGAGGTGCTGTGTGGATGGATGAGGTGCTGGT TGTGGATGGATGAGATGCTGGTGTGTGGATGGTTGAGGTGCTGTGTGGATGGATGAGGTGCTGGT T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87738447..87738670 26863196 MeRIP-seq:(Medium) rs552071077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503021,Human_RBP_ID_5647102,Human_RBP_ID_17256197,Human_RBP_ID_23705600,Human_RBP_ID_27837925 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79107 RMVar_ID_79107 Human_SNP_ID_613392959 m1A Human chr16 - 87739315 87739312 87739316 TGTGGATGGATGAGATGCTGTTGTGTGGATGGATGAGGTGCTGGTGTGTGGATGGATGAGGTGCT TGTGGATGGATGAGATGCTGTTGTGTGGATG____AGGTGCTGGTGTGTGGATGGATGAGGTGCT TCATC T KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:87739220..87739405 26863196 MeRIP-seq:(Medium) rs1292752503 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5647106,Human_RBP_ID_8441289,Human_RBP_ID_17256490,Human_RBP_ID_23705617 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79108 RMVar_ID_79108 Human_SNP_ID_613392964 m1A Human chr16 + 87739327 87739325 87739327 ATCCACACACCAGCACCTCATCCATCCACACAACAGCATCTCATCCATCCACACACCAGCATCTC ATCCACACACCAGCACCTCATCCATCCACAC__CAGCATCTCATCCATCCACACACCAGCATCTC CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87739281..87739505;chr16:87739280..87739518;chr16:87739258..87739528 26863196 MeRIP-seq:(Medium) rs1214453664 Functional Loss DEL dbSNP153 32..33 33 - - - 79109 RMVar_ID_79109 Human_SNP_ID_613392965 m1A Human chr16 + 87739327 87739327 87739327 ATCCACACACCAGCACCTCATCCATCCACACAACAGCATCTCATCCATCCACACACCAGCATCTC ATCCACACACCAGCACCTCATCCATCCACACACCAGCATCTCATCCATCCACACACCAGCATCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87739281..87739505;chr16:87739280..87739518;chr16:87739258..87739528 26863196 MeRIP-seq:(Medium) rs868750821 Functional Loss SNV dbSNP153 33..33 33 - - - 79110 RMVar_ID_79110 Human_SNP_ID_613393117 m1A Human chr16 - 87739625 87739622 87739626 TGTGGATGTATGACGTGCTGGTGTGTGGATGGATGACGTGCTGGTGTGTGGATGGATGACGTGCT TGTGGATGTATGACGTGCTGGTGTGTGGATG____ACGTGCTGGTGTGTGGATGGATGACGTGCT TCATC T KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87739574..87739669 26863196 MeRIP-seq:(Medium) rs1555582326 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_23705628 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79111 RMVar_ID_79111 Human_SNP_ID_613395457 m1A Human chr16 + 87745228 87745228 87745228 ACCCTACACCCATATTGCCCAGCACTGCTCTCACAACACCCGCCCTGGGGCCGGCCATAGGGTGC ACCCTACACCCATATTGCCCAGCACTGCTCTCGCAACACCCGCCCTGGGGCCGGCCATAGGGTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87745219..87745429 26863196 MeRIP-seq:(Medium) rs1236057620 Functional Loss SNV dbSNP153 33..33 33 - - - 79112 RMVar_ID_79112 Human_SNP_ID_613395470 m1A Human chr16 - 87745263 87745263 87745263 GGCGGGTGCTGCAAGAGCAGAAGGCGGAGCAGAGGGCACCCTATGGCCGGCCCCAGGGCGGGTGT GGCGGGTGCTGCAAGAGCAGAAGGCGGAGCAGGGGGCACCCTATGGCCGGCCCCAGGGCGGGTGT T C KLHDC4,AC010536.2 Ensembl:ENSG00000104731,Ensembl:ENSG00000260671 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:87745213..87745444 26863196 MeRIP-seq:(Medium) rs8059456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261696,Human_RBP_ID_5647126,Human_RBP_ID_8184946,Human_RBP_ID_9420825,Human_RBP_ID_12839373 GWAS_ID_9518,GWAS_ID_9519,GWAS_ID_9520,GWAS_ID_9521,GWAS_ID_9522,GWAS_ID_9523,GWAS_ID_9524,GWAS_ID_9525,GWAS_ID_9526,GWAS_ID_9527,GWAS_ID_9528,GWAS_ID_9529,GWAS_ID_9530,GWAS_ID_9531 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 79113 RMVar_ID_79113 Human_SNP_ID_613402883 m1A Human chr16 - 87762038 87762038 87762038 GTCTCACGTGTGCCTGCTTGCTTGCCCTAGGAAGACCTGGAAGCGCTCATAGCCCATTTCCAGAC GTCTCACGTGTGCCTGCTTGCTTGCCCTAGGAGGACCTGGAAGCGCTCATAGCCCATTTCCAGAC T C KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87761976..87762102 26863196 MeRIP-seq:(Medium) rs1278861113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761157,Human_RBP_ID_9373320,Human_RBP_ID_12839959,Human_RBP_ID_18987107,Human_RBP_ID_22945156 Human_Splice_Rec_1748352,Human_Splice_Rec_1748353,Human_Splice_Rec_1748418,Human_Splice_Rec_1748419,Human_Splice_Rec_1748438,Human_Splice_Rec_1748439,Human_Splice_Rec_1748478,Human_Splice_Rec_1748479,Human_Splice_Rec_1748498,Human_Splice_Rec_1748499,Human_Splice_Rec_1748529,Human_Splice_Rec_1748557,Human_Splice_Rec_1748563,Human_Splice_Rec_1748572,Human_Splice_Rec_1748573,Human_Splice_Rec_1748582,Human_Splice_Rec_1748583,Human_Splice_Rec_1748593,Human_Splice_Rec_1748600,Human_Splice_Rec_1748601,Human_Splice_Rec_1748609,Human_Splice_Rec_1748616 RMVar_hsa_circ_1888,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180440,RMVar_hsa_circ_270380,RMVar_hsa_circ_180445,RMVar_hsa_circ_339846 79114 RMVar_ID_79114 Human_SNP_ID_613404684 m1A Human chr16 - 87765868 87765866 87765869 ACCCGGCAAGATGGGCAAGAAGGGCAAGAAGGAGAAGAAGGGCCGCGGCGCGGAGAAGACGGCCG ACCCGGCAAGATGGGCAAGAAGGGCAAGAAG___AAGAAGGGCCGCGGCGCGGAGAAGACGGCCG TCTC T KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:87765770..87765957 26863196 MeRIP-seq:(Medium) rs774776543 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_46134,Human_RBP_ID_763608,Human_RBP_ID_892751,Human_RBP_ID_4394068,Human_RBP_ID_9373322,Human_RBP_ID_18987111,Human_RBP_ID_22944711,Human_RBP_ID_24544551 Human_Splice_Rec_1748351,Human_Splice_Rec_1748399,Human_Splice_Rec_1748417,Human_Splice_Rec_1748437,Human_Splice_Rec_1748477,Human_Splice_Rec_1748497,Human_Splice_Rec_1748517,Human_Splice_Rec_1748555,Human_Splice_Rec_1748571,Human_Splice_Rec_1748581,Human_Splice_Rec_1748591,Human_Splice_Rec_1748597,Human_Splice_Rec_1748607,Human_Splice_Rec_1748613,Human_Splice_Rec_1748617 79115 RMVar_ID_79115 Human_SNP_ID_613404687 m1A Human chr16 - 87765868 87765868 87765868 ACCCGGCAAGATGGGCAAGAAGGGCAAGAAGGAGAAGAAGGGCCGCGGCGCGGAGAAGACGGCCG ACCCGGCAAGATGGGCAAGAAGGGCAAGAAGGCGAAGAAGGGCCGCGGCGCGGAGAAGACGGCCG T G KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:87765770..87765957 26863196 MeRIP-seq:(Medium) rs1001391348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46134,Human_RBP_ID_763608,Human_RBP_ID_892751,Human_RBP_ID_4394068,Human_RBP_ID_9373322,Human_RBP_ID_18987111,Human_RBP_ID_22944711,Human_RBP_ID_24544551 Human_Splice_Rec_1748351,Human_Splice_Rec_1748399,Human_Splice_Rec_1748417,Human_Splice_Rec_1748437,Human_Splice_Rec_1748477,Human_Splice_Rec_1748497,Human_Splice_Rec_1748517,Human_Splice_Rec_1748555,Human_Splice_Rec_1748571,Human_Splice_Rec_1748581,Human_Splice_Rec_1748591,Human_Splice_Rec_1748597,Human_Splice_Rec_1748607,Human_Splice_Rec_1748613,Human_Splice_Rec_1748617 79116 RMVar_ID_79116 Human_SNP_ID_613404718 m1A Human chr16 + 87765905 87765905 87765905 CTTGCCCTTCTTGCCCATCTTGCCGGGTCCCAAGCCGCGACGGGACACCAGGAAAGAAAACGGCC CTTGCCCTTCTTGCCCATCTTGCCGGGTCCCACGCCGCGACGGGACACCAGGAAAGAAAACGGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:87765760..87765975;chr16:87765776..87765975 26863196 MeRIP-seq:(Medium) rs751321830 Functional Loss SNV dbSNP153 33..33 33 - - - 79117 RMVar_ID_79117 Human_SNP_ID_613404719 m1A Human chr16 + 87765905 87765905 87765905 CTTGCCCTTCTTGCCCATCTTGCCGGGTCCCAAGCCGCGACGGGACACCAGGAAAGAAAACGGCC CTTGCCCTTCTTGCCCATCTTGCCGGGTCCCATGCCGCGACGGGACACCAGGAAAGAAAACGGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:87765760..87765975;chr16:87765776..87765975 26863196 MeRIP-seq:(Medium) rs751321830 Functional Loss SNV dbSNP153 33..33 33 - - - 79118 RMVar_ID_79118 Human_SNP_ID_613404724 m1A Human chr16 + 87765912 87765912 87765912 TTCTTGCCCATCTTGCCGGGTCCCAAGCCGCGACGGGACACCAGGAAAGAAAACGGCCCGCGCTC TTCTTGCCCATCTTGCCGGGTCCCAAGCCGCGGCGGGACACCAGGAAAGAAAACGGCCCGCGCTC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:87765818..87765951 26863196 MeRIP-seq:(Medium) rs1224828213 Functional Loss SNV dbSNP153 33..33 33 - - - 79119 RMVar_ID_79119 Human_SNP_ID_613409726 m1A Human chr16 - 87778500 87778491 87778501 AAGAGAGAGACAGAGGAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAGAAAGAAAGAAAGA AAGAGAGAGACAGAGGAAGAAGAAAGAAAGA__________GAGAGAGAGAGAAAGAAAGAAAGA CTCTCTCTCTT C AC126696.3 Ensembl:ENSG00000260498 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87778492..87778624 26863196 MeRIP-seq:(Medium) rs1200368029 Functional Loss DEL dbSNP153 32..41 33 - - - 79120 RMVar_ID_79120 Human_SNP_ID_613409731 m1A Human chr16 - 87778500 87778495 87778501 AAGAGAGAGACAGAGGAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAGAAAGAAAGAAAGA AAGAGAGAGACAGAGGAAGAAGAAAGAAAGA______GAGAGAGAGAGAGAGAAAGAAAGAAAGA CTCTCTT C AC126696.3 Ensembl:ENSG00000260498 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87778492..87778624 26863196 MeRIP-seq:(Medium) rs1178802105 Functional Loss DEL dbSNP153 32..37 33 - - - 79121 RMVar_ID_79121 Human_SNP_ID_613409736 m1A Human chr16 - 87778500 87778497 87778501 AAGAGAGAGACAGAGGAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAGAAAGAAAGAAAGA AAGAGAGAGACAGAGGAAGAAGAAAGAAAGA____GAGAGAGAGAGAGAGAGAAAGAAAGAAAGA CTCTT C AC126696.3 Ensembl:ENSG00000260498 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87778492..87778624 26863196 MeRIP-seq:(Medium) rs1555615707 Functional Loss DEL dbSNP153 32..35 33 - - - 79122 RMVar_ID_79122 Human_SNP_ID_613409739 m1A Human chr16 - 87778500 87778499 87778501 AAGAGAGAGACAGAGGAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAGAGAGAAAGAAAGAAAGA AAGAGAGAGACAGAGGAAGAAGAAAGAAAGA__GAGAGAGAGAGAGAGAGAGAAAGAAAGAAAGA CTT C AC126696.3 Ensembl:ENSG00000260498 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87778492..87778624 26863196 MeRIP-seq:(Medium) rs1168526005 Functional Loss DEL dbSNP153 32..33 33 - - - 79123 RMVar_ID_79123 Human_SNP_ID_613428506 m1A Human chr16 - 87831882 87831882 87831882 TGATGCCCGTTGTCTAGGAGACAGAGCCAAGCACTGCTCACGTCTCTGCCGCCTGCGTTTGGAGG TGATGCCCGTTGTCTAGGAGACAGAGCCAAGCGCTGCTCACGTCTCTGCCGCCTGCGTTTGGAGG T C SLC7A5 Ensembl:ENSG00000103257 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87831832..87832095 26863196 MeRIP-seq:(Medium) rs1320923355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481403,Human_RBP_ID_1089091,Human_RBP_ID_1524279,Human_RBP_ID_4388524,Human_RBP_ID_5236765,Human_RBP_ID_6544860,Human_RBP_ID_17882398,Human_RBP_ID_20094454,Human_RBP_ID_22498539,Human_RBP_ID_26444229,Human_RBP_ID_27446866 Human_miRNA_ID_327284,Human_miRNA_ID_331309,Human_miRNA_ID_348405,Human_miRNA_ID_1511449,Human_miRNA_ID_1641681,Human_miRNA_ID_2843843 RMVar_hsa_circ_85964,RMVar_hsa_circ_108585,RMVar_hsa_circ_112778,RMVar_hsa_circ_110242,RMVar_hsa_circ_95583,RMVar_hsa_circ_105531,RMVar_hsa_circ_91533,RMVar_hsa_circ_180447,RMVar_hsa_circ_180451,RMVar_hsa_circ_80127,RMVar_hsa_circ_81631,RMVar_hsa_circ_180453,RMVar_hsa_circ_180454,RMVar_hsa_circ_180452,RMVar_hsa_circ_180449,RMVar_hsa_circ_180450,RMVar_hsa_circ_180448,RMVar_hsa_circ_180446 79124 RMVar_ID_79124 Human_SNP_ID_613428652 m1A Human chr16 - 87832340 87832340 87832340 GTGATTCCTCCCAGGAGGTGCTTGAGGCCCCGATGGACTCCTGACCATAATCCTAGCCCCGAGAC GTGATTCCTCCCAGGAGGTGCTTGAGGCCCCGGTGGACTCCTGACCATAATCCTAGCCCCGAGAC T C SLC7A5 Ensembl:ENSG00000103257 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87832291..87832455 26863196 MeRIP-seq:(Medium) rs1320412495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44298,Human_RBP_ID_261083,Human_RBP_ID_482801,Human_RBP_ID_1089093,Human_RBP_ID_1283766,Human_RBP_ID_1524290,Human_RBP_ID_2488812,Human_RBP_ID_3948029,Human_RBP_ID_4393306,Human_RBP_ID_5142009,Human_RBP_ID_5524725,Human_RBP_ID_6544873,Human_RBP_ID_8187274,Human_RBP_ID_8441397,Human_RBP_ID_8941403,Human_RBP_ID_9326188,Human_RBP_ID_9353256,Human_RBP_ID_12840371,Human_RBP_ID_17882402,Human_RBP_ID_20094459,Human_RBP_ID_22053540,Human_RBP_ID_24477282,Human_RBP_ID_26444251,Human_RBP_ID_26951449,Human_RBP_ID_27247871,Human_RBP_ID_27446883 RMVar_hsa_circ_85964,RMVar_hsa_circ_108585,RMVar_hsa_circ_112778,RMVar_hsa_circ_110242,RMVar_hsa_circ_95583,RMVar_hsa_circ_105531,RMVar_hsa_circ_91533,RMVar_hsa_circ_180447,RMVar_hsa_circ_180451,RMVar_hsa_circ_80127,RMVar_hsa_circ_81631,RMVar_hsa_circ_180453,RMVar_hsa_circ_180454,RMVar_hsa_circ_180452,RMVar_hsa_circ_180449,RMVar_hsa_circ_180450,RMVar_hsa_circ_180448,RMVar_hsa_circ_180446 79125 RMVar_ID_79125 Human_SNP_ID_613428833 m1A Human chr16 - 87832927 87832927 87832927 GAGTGGCTGCCGGAGGAGCATGCGCAGAGGCCAGTTAAAGTAGATCACCTCCTCGAACCCACTCC GAGTGGCTGCCGGAGGAGCATGCGCAGAGGCCGGTTAAAGTAGATCACCTCCTCGAACCCACTCC T C SLC7A5 Ensembl:ENSG00000103257 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:87832876..87832975 32194978 MeRIP-seq:(Medium) rs1248752446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481429,Human_RBP_ID_1005858,Human_RBP_ID_1524314,Human_RBP_ID_6544901,Human_RBP_ID_12840428,Human_RBP_ID_17882413,Human_RBP_ID_18686433,Human_RBP_ID_22441154,Human_RBP_ID_27446908 Human_Splice_Rec_1748656,Human_Splice_Rec_1748674,Human_Splice_Rec_1748678 Human_miRNA_ID_470992,Human_miRNA_ID_476839,Human_miRNA_ID_1797884,Human_miRNA_ID_2156217,Human_miRNA_ID_2159778 RMVar_hsa_circ_85964,RMVar_hsa_circ_108585,RMVar_hsa_circ_112778,RMVar_hsa_circ_110242,RMVar_hsa_circ_95583,RMVar_hsa_circ_105531,RMVar_hsa_circ_91533,RMVar_hsa_circ_180447,RMVar_hsa_circ_180451,RMVar_hsa_circ_80127,RMVar_hsa_circ_81631,RMVar_hsa_circ_180453,RMVar_hsa_circ_180454,RMVar_hsa_circ_180452,RMVar_hsa_circ_180449,RMVar_hsa_circ_180450,RMVar_hsa_circ_180448,RMVar_hsa_circ_180446 79126 RMVar_ID_79126 Human_SNP_ID_613430438 m1A Human chr16 - 87837075 87837075 87837075 GGGCAGCAAGTCCTGGACTCTTTGGCAGCTGCACGGTCCTCGGGAGCACGGCTGTGCCGGGGGTT GGGCAGCAAGTCCTGGACTCTTTGGCAGCTGCGCGGTCCTCGGGAGCACGGCTGTGCCGGGGGTT T C SLC7A5 Ensembl:ENSG00000103257 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87837073..87837162 26863196 MeRIP-seq:(Medium) rs532617229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44240,RMVar_hsa_circ_112778,RMVar_hsa_circ_110242,RMVar_hsa_circ_95583,RMVar_hsa_circ_105531,RMVar_hsa_circ_180447,RMVar_hsa_circ_180451,RMVar_hsa_circ_80127,RMVar_hsa_circ_81631,RMVar_hsa_circ_180449,RMVar_hsa_circ_180450,RMVar_hsa_circ_180448,RMVar_hsa_circ_180446,RMVar_hsa_circ_99855,RMVar_hsa_circ_180455 79127 RMVar_ID_79127 Human_SNP_ID_613431016 m1A Human chr16 + 87838813 87838813 87838813 TCCAGGACATGACGCCCAGGTGATAGTTCCCGAAGTCCTAGGCAGGCACAACCAGTGAGCTGGGC TCCAGGACATGACGCCCAGGTGATAGTTCCCGTAGTCCTAGGCAGGCACAACCAGTGAGCTGGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87838667..87838874 26863196 MeRIP-seq:(Medium) rs772727258 Functional Loss SNV dbSNP153 33..33 33 - - - 79128 RMVar_ID_79128 Human_SNP_ID_613431845 m1A Human chr16 + 87841147 87841147 87841147 GCCTTCAAATGAGAAGTTGGGATCTAGATTGGACACATCACCTGGCAGGGCCAAAGAAAGGAATG GCCTTCAAATGAGAAGTTGGGATCTAGATTGGTCACATCACCTGGCAGGGCCAAAGAAAGGAATG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87841006..87841206 26863196 MeRIP-seq:(Medium) rs1453260294 Functional Loss SNV dbSNP153 33..33 33 - - - 79129 RMVar_ID_79129 Human_SNP_ID_613433313 m1A Human chr16 + 87845465 87845465 87845465 CCCACCCCAGAGTCCATGCCCACTCCAGGCAGAGTCCACGCCCACCCCACAGAGTCCACGCCCAC CCCACCCCAGAGTCCATGCCCACTCCAGGCAGGGTCCACGCCCACCCCACAGAGTCCACGCCCAC A G NONHSAG020263.2 RNACentral:URS00009B3A26 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87845463..87845647 26863196 MeRIP-seq:(Medium) rs1356694204 Functional Loss SNV dbSNP153 33..33 33 - - - 79130 RMVar_ID_79130 Human_SNP_ID_613433325 m1A Human chr16 + 87845485 87845485 87845485 CACTCCAGGCAGAGTCCACGCCCACCCCACAGAGTCCACGCCCACCCCAGAGTCCATGCCCACTC CACTCCAGGCAGAGTCCACGCCCACCCCACAGGGTCCACGCCCACCCCAGAGTCCATGCCCACTC A G NONHSAG020263.2 RNACentral:URS00009B3A26 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:87845326..87845600 26863196 MeRIP-seq:(Medium) rs1316220749 Functional Loss SNV dbSNP153 33..33 33 - - - 79131 RMVar_ID_79131 Human_SNP_ID_613441572 m1A Human chr16 + 87868902 87868902 87868902 GCGCCCCGTACTCACGCACGCAGAGGCAGGCCACGAGCTTGGCTGCCTCCTCGGGCACCGGGCAG GCGCCCCGTACTCACGCACGCAGAGGCAGGCCGCGAGCTTGGCTGCCTCCTCGGGCACCGGGCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:87868876..87868950 32194978 MeRIP-seq:(Medium) rs1397184995 Functional Loss SNV dbSNP153 33..33 33 - - - 79132 RMVar_ID_79132 Human_SNP_ID_613441640 m1A Human chr16 - 87869076 87869076 87869076 GCTCGGCACCACCATCTCCAAATCGGGCGGCGACTACGCCTACATGCTGGAGGTCTACGGCTCGC GCTCGGCACCACCATCTCCAAATCGGGCGGCGGCTACGCCTACATGCTGGAGGTCTACGGCTCGC T C SLC7A5 Ensembl:ENSG00000103257 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87869034..87869175 26863196 MeRIP-seq:(Medium) rs776542767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8441539,Human_RBP_ID_18207542,Human_RBP_ID_27446954 Human_miRNA_ID_2442088 RMVar_hsa_circ_110242,RMVar_hsa_circ_180446 79133 RMVar_ID_79133 Human_SNP_ID_613441839 m1A Human chr16 + 87869414 87869414 87869414 GGCGCCGCTAGCGCGCGCCGCTTCGGGCCCGCACCCGCCATGCTCTGCGCACCGGCCGGGCCTGG GGCGCCGCTAGCGCGCGCCGCTTCGGGCCCGCCCCCGCCATGCTCTGCGCACCGGCCGGGCCTGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:87869076..87869500 26863410 MeRIP-seq:(Medium) rs756662169 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 79134 RMVar_ID_79134 Human_SNP_ID_613441867 m1A Human chr16 - 87869444 87869444 87869444 CTGCTCGCTGGGCCGCGGCTCCCGGGTGTCCCAGGCCCGGCCGGTGCGCAGAGCATGGCGGGTGC CTGCTCGCTGGGCCGCGGCTCCCGGGTGTCCCTGGCCCGGCCGGTGCGCAGAGCATGGCGGGTGC T A SLC7A5 Ensembl:ENSG00000103257 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:87869395..87869485 26863410 MeRIP-seq:(Medium) rs954334203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46416,Human_RBP_ID_4388652,Human_RBP_ID_5274731,Human_RBP_ID_17882436,Human_RBP_ID_23128841,Human_RBP_ID_27446961,Human_RBP_ID_27812027 RMVar_hsa_circ_110242,RMVar_hsa_circ_180446 79135 RMVar_ID_79135 Human_SNP_ID_613472433 m1A Human chr16 + 87951524 87951524 87951524 CACGAGAATTCCGCAGCCCACACGGTAATTGCAGCTCCCGCAGCCGGTCGCGCCTCCGCCTCCCC CACGAGAATTCCGCAGCCCACACGGTAATTGCGGCTCCCGCAGCCGGTCGCGCCTCCGCCTCCCC A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87951501..87951874 26863196 MeRIP-seq:(Medium) rs1179180779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85665,RMVar_hsa_circ_180460 79136 RMVar_ID_79136 Human_SNP_ID_613472522 m1A Human chr16 + 87951665 87951665 87951665 GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGATCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGCTCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC A C BANP Ensembl:ENSG00000172530 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87951573..87951750 26863410 MeRIP-seq:(Medium) rs549143184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780772 RMVar_hsa_circ_85665,RMVar_hsa_circ_180460 79137 RMVar_ID_79137 Human_SNP_ID_613472523 m1A Human chr16 + 87951665 87951665 87951665 GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGATCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGGTCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87951573..87951750 26863410 MeRIP-seq:(Medium) rs549143184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780772 RMVar_hsa_circ_85665,RMVar_hsa_circ_180460 79138 RMVar_ID_79138 Human_SNP_ID_613472524 m1A Human chr16 + 87951665 87951665 87951665 GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGATCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGTTCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC A T BANP Ensembl:ENSG00000172530 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87951573..87951750 26863410 MeRIP-seq:(Medium) rs549143184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780772 RMVar_hsa_circ_85665,RMVar_hsa_circ_180460 79139 RMVar_ID_79139 Human_SNP_ID_613474496 m1A Human chr16 + 87957283 87957283 87957283 CAGGTCGCCAGCTTACAGCGTGGGAGCTGTGGAAGGACACATGGAGCAGAGGCGGCTGAGGAGGT CAGGTCGCCAGCTTACAGCGTGGGAGCTGTGGTAGGACACATGGAGCAGAGGCGGCTGAGGAGGT A T BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87957275..87957378 26863196 MeRIP-seq:(Medium) rs1567572415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85665,RMVar_hsa_circ_27539,RMVar_hsa_circ_180460 79140 RMVar_ID_79140 Human_SNP_ID_613477154 m1A Human chr16 - 87965068 87965068 87965068 CCCTGGAACCTTTGCTCAGCCAGCACTGACCCAGCGGCTCATCAGTCTGTGGCTTCAGATACATC CCCTGGAACCTTTGCTCAGCCAGCACTGACCCGGCGGCTCATCAGTCTGTGGCTTCAGATACATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87965049..87965570 26863196 MeRIP-seq:(Medium) rs960273188 Functional Loss SNV dbSNP153 33..33 33 - - - 79141 RMVar_ID_79141 Human_SNP_ID_613484083 m1A Human chr16 - 87985086 87985086 87985086 CACACGGGCAGCGAGGTCACAACAGTCCCTCCAGGCTTGTTGCGGCTCCCATTCCTCGGCGTCCA CACACGGGCAGCGAGGTCACAACAGTCCCTCCCGGCTTGTTGCGGCTCCCATTCCTCGGCGTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87985080..87985145 26863196 MeRIP-seq:(Medium) rs1339580470 Functional Loss SNV dbSNP153 33..33 33 - - - 79142 RMVar_ID_79142 Human_SNP_ID_613485566 m1A Human chr16 - 87989661 87989661 87989661 TGTCCTGGATATGCGCAGCCACGCGGGCCTGCATCCCCCATCACCCGCCCTGTGTCCTGTGTCCT TGTCCTGGATATGCGCAGCCACGCGGGCCTGCGTCCCCCATCACCCGCCCTGTGTCCTGTGTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87989655..87989771 26863196 MeRIP-seq:(Medium) rs1461336339 Functional Loss SNV dbSNP153 33..33 33 - - - 79143 RMVar_ID_79143 Human_SNP_ID_613485603 m1A Human chr16 - 87989732 87989732 87989732 CCCTGTGTCCTGTGTCCTGGATGCGCGCAGCCACGCGGGCCTGCATCCCCCGTCGCCCACCCTGT CCCTGTGTCCTGTGTCCTGGATGCGCGCAGCCGCGCGGGCCTGCATCCCCCGTCGCCCACCCTGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87989696..87989882 26863196 MeRIP-seq:(Medium) rs1226507293 Functional Loss SNV dbSNP153 33..33 33 - - - 79144 RMVar_ID_79144 Human_SNP_ID_613485620 m1A Human chr16 - 87989831 87989772 87989831 GATGCACGCAGCCACGCGGGCCTGCATCCCCCATCACCCGCCCTGTGTCCTGTGTCCTGGATGCG GATGCACGCAGCCACGCGGGCCTGCATCCCCC_________________________________ CGGGGGATGCAGGCCCGCGTGGCTGCGCGCATCCAGGACACAGGACACAGGGCGGGTGAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87989826..87989910 26863196 MeRIP-seq:(Medium) rs1567678968 Functional Loss DEL dbSNP153 33..65 33 - - - 79145 RMVar_ID_79145 Human_SNP_ID_613485644 m1A Human chr16 - 87989831 87989831 87989831 GATGCACGCAGCCACGCGGGCCTGCATCCCCCATCACCCGCCCTGTGTCCTGTGTCCTGGATGCG GATGCACGCAGCCACGCGGGCCTGCATCCCCCGTCACCCGCCCTGTGTCCTGTGTCCTGGATGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87989826..87989910 26863196 MeRIP-seq:(Medium) rs369714845 Functional Loss SNV dbSNP153 33..33 33 - - - 79146 RMVar_ID_79146 Human_SNP_ID_613485645 m1A Human chr16 - 87989831 87989831 87989831 GATGCACGCAGCCACGCGGGCCTGCATCCCCCATCACCCGCCCTGTGTCCTGTGTCCTGGATGCG GATGCACGCAGCCACGCGGGCCTGCATCCCCCCTCACCCGCCCTGTGTCCTGTGTCCTGGATGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:87989826..87989910 26863196 MeRIP-seq:(Medium) rs369714845 Functional Loss SNV dbSNP153 33..33 33 - - - 79147 RMVar_ID_79147 Human_SNP_ID_613487952 m1A Human chr16 - 87997580 87997580 87997580 CCAGCCATCCTGGCTATTTTACCCACTTTACCACGAACACATGGTCTCACTCCCAGCCATCCTGG CCAGCCATCCTGGCTATTTTACCCACTTTACCGCGAACACATGGTCTCACTCCCAGCCATCCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:87997486..87997788 26863196 MeRIP-seq:(Medium) rs750179290 Functional Loss SNV dbSNP153 33..33 33 - - - 79148 RMVar_ID_79148 Human_SNP_ID_613490440 m1A Human chr16 + 88005213 88005213 88005213 TTGGTGATGGGCGGTGAGGAGGTGCCAGGGTCAGCTGTGCCTCAGGGGCTTTGCACTGAGGTCAG TTGGTGATGGGCGGTGAGGAGGTGCCAGGGTCCGCTGTGCCTCAGGGGCTTTGCACTGAGGTCAG A C BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88005209..88005274 26863196 MeRIP-seq:(Medium) rs559058465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4168,RMVar_hsa_circ_180461,RMVar_hsa_circ_89750,RMVar_hsa_circ_180465,RMVar_hsa_circ_286907,RMVar_hsa_circ_296891,RMVar_hsa_circ_282127,RMVar_hsa_circ_94686,RMVar_hsa_circ_180463,RMVar_hsa_circ_180464,RMVar_hsa_circ_315890,RMVar_hsa_circ_180462,RMVar_hsa_circ_76383,RMVar_hsa_circ_96595,RMVar_hsa_circ_180469,RMVar_hsa_circ_291690,RMVar_hsa_circ_349528,RMVar_hsa_circ_180471,RMVar_hsa_circ_304906,RMVar_hsa_circ_281829,RMVar_hsa_circ_180473,RMVar_hsa_circ_180474,RMVar_hsa_circ_180475,RMVar_hsa_circ_180472 79149 RMVar_ID_79149 Human_SNP_ID_613495360 m1A Human chr16 + 88020740 88020739 88020741 GTGAGGAGTCCCTGCTCCTCGGGGGAGAAGACAGGGGCCTTGGATGTGAAGCTGGAGGCCGGCTG GTGAGGAGTCCCTGCTCCTCGGGGGAGAAGAC__GGGCCTTGGATGTGAAGCTGGAGGCCGGCTG CAG C BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88020699..88020818 26863196 MeRIP-seq:(Medium) rs1288643138 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_282127,RMVar_hsa_circ_94686,RMVar_hsa_circ_180463,RMVar_hsa_circ_180462,RMVar_hsa_circ_76383,RMVar_hsa_circ_349528,RMVar_hsa_circ_281829,RMVar_hsa_circ_51887,RMVar_hsa_circ_180473,RMVar_hsa_circ_320485,RMVar_hsa_circ_180472,RMVar_hsa_circ_286504,RMVar_hsa_circ_318607,RMVar_hsa_circ_344519,RMVar_hsa_circ_277184,RMVar_hsa_circ_39446,RMVar_hsa_circ_180477 79150 RMVar_ID_79150 Human_SNP_ID_613495361 m1A Human chr16 + 88020740 88020740 88020740 GTGAGGAGTCCCTGCTCCTCGGGGGAGAAGACAGGGGCCTTGGATGTGAAGCTGGAGGCCGGCTG GTGAGGAGTCCCTGCTCCTCGGGGGAGAAGACGGGGGCCTTGGATGTGAAGCTGGAGGCCGGCTG A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88020699..88020818 26863196 MeRIP-seq:(Medium) rs1418270915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282127,RMVar_hsa_circ_94686,RMVar_hsa_circ_180463,RMVar_hsa_circ_180462,RMVar_hsa_circ_76383,RMVar_hsa_circ_349528,RMVar_hsa_circ_281829,RMVar_hsa_circ_51887,RMVar_hsa_circ_180473,RMVar_hsa_circ_320485,RMVar_hsa_circ_180472,RMVar_hsa_circ_286504,RMVar_hsa_circ_318607,RMVar_hsa_circ_344519,RMVar_hsa_circ_277184,RMVar_hsa_circ_39446,RMVar_hsa_circ_180477 79151 RMVar_ID_79151 Human_SNP_ID_613501148 m1A Human chr16 - 88038171 88038171 88038171 CCCCACCCCTCGGCAGCGCAATGCCCACAATGACCGTCCCACCCCTCCCGTGAGAGCCCCACCCC CCCCACCCCTCGGCAGCGCAATGCCCACAATGCCCGTCCCACCCCTCCCGTGAGAGCCCCACCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88038169..88038365;chr16:88038161..88038340 26863196 MeRIP-seq:(Medium) rs1405840441 Functional Loss SNV dbSNP153 33..33 33 - - - 79152 RMVar_ID_79152 Human_SNP_ID_613502475 m1A Human chr16 + 88041984 88041984 88041984 GGTGAGAGACGCAGTAGGAGGGTGAGAGACGCAGTAGGAGCGTGGGAGACGCAGTAGGAGGGTGA GGTGAGAGACGCAGTAGGAGGGTGAGAGACGCCGTAGGAGCGTGGGAGACGCAGTAGGAGGGTGA A C BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88041908..88042048 26863196 MeRIP-seq:(Medium) rs1481214012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344519,RMVar_hsa_circ_345911,RMVar_hsa_circ_370379,RMVar_hsa_circ_180482,RMVar_hsa_circ_180483,RMVar_hsa_circ_10036 79153 RMVar_ID_79153 Human_SNP_ID_613506013 m1A Human chr16 + 88052615 88052615 88052615 ACACAACCACCTCTACCACCTCCGCCACTGTCATCTCCATCATCCTCACCATTATCATAATTGCC ACACAACCACCTCTACCACCTCCGCCACTGTCGTCTCCATCATCCTCACCATTATCATAATTGCC A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88052610..88052803 26863196 MeRIP-seq:(Medium) rs914562918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199509,Human_RBP_ID_2489204,Human_RBP_ID_9421706,Human_RBP_ID_17653124,Human_RBP_ID_24531682,Human_RBP_ID_26757550 RMVar_hsa_circ_344519,RMVar_hsa_circ_345911,RMVar_hsa_circ_370379,RMVar_hsa_circ_180482,RMVar_hsa_circ_180483,RMVar_hsa_circ_10036 79154 RMVar_ID_79154 Human_SNP_ID_613508026 m1A Human chr16 + 88057777 88057777 88057777 TGGGTGGGGCGGGGGGGGGGGTGCGTGCAGTGACTCGCGCTGGCCCTGTCCCCGCACCCTGGACT TGGGTGGGGCGGGGGGGGGGGTGCGTGCAGTGCCTCGCGCTGGCCCTGTCCCCGCACCCTGGACT A C BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88057772..88057891 26863196 MeRIP-seq:(Medium) rs1379313842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505148,Human_RBP_ID_12842377,Human_RBP_ID_18482981,Human_RBP_ID_26780777 RMVar_hsa_circ_344519,RMVar_hsa_circ_345911,RMVar_hsa_circ_370379,RMVar_hsa_circ_180482,RMVar_hsa_circ_180483,RMVar_hsa_circ_10036 79155 RMVar_ID_79155 Human_SNP_ID_613510130 m1A Human chr16 + 88064101 88064101 88064101 TGCCTTGGAACAAGGTGTGGGGGCCAACCACAAGCAGGCACCGGCGCTGGGGGACCAGGGTCAGG TGCCTTGGAACAAGGTGTGGGGGCCAACCACATGCAGGCACCGGCGCTGGGGGACCAGGGTCAGG A T BANP Ensembl:ENSG00000172530 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88064095..88064240 26863196 MeRIP-seq:(Medium) rs1388774563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344519,RMVar_hsa_circ_345911,RMVar_hsa_circ_370379,RMVar_hsa_circ_180482,RMVar_hsa_circ_180483,RMVar_hsa_circ_10036 79156 RMVar_ID_79156 Human_SNP_ID_613598534 m1A Human chr16 + 88331299 88331299 88331299 TCATAGTCATCATCATCACCATCACCACCATCACCATCATTATCATCATTGTTACCATGACCATC TCATAGTCATCATCATCACCATCACCACCATCGCCATCATTATCATCATTGTTACCATGACCATC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88331253..88331336 26863196 MeRIP-seq:(Medium) rs1198234283 Functional Loss SNV dbSNP153 33..33 33 - - - 79157 RMVar_ID_79157 Human_SNP_ID_613598725 m1A Human chr16 + 88331652 88331652 88331652 TCACTATTGTTACCACCGCCATCATCATCACCACCATCATCATCTTCATCACCACCATCACTATT TCACTATTGTTACCACCGCCATCATCATCACCGCCATCATCATCTTCATCACCACCATCACTATT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88331634..88331730 26863196 MeRIP-seq:(Medium) rs1288015032 Functional Loss SNV dbSNP153 33..33 33 - - - 79158 RMVar_ID_79158 Human_SNP_ID_613611281 m1A Human chr16 + 88371959 88371924 88371960 TCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACC __________________________________CATCACCATCACCACCATCATCACCATCACC CCATCACCATCACCACCATCATCACCATCACCACCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88371917..88372008 26863196 MeRIP-seq:(Medium) rs1469708544 Functional Loss DEL dbSNP153 1..34 33 - - - 79159 RMVar_ID_79159 Human_SNP_ID_613611282 m1A Human chr16 + 88371959 88371924 88371960 TCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACC TCACCATCACCACCAT__________________CATCACCATCACCACCATCATCACCATCACC CCATCACCATCACCACCATCATCACCATCACCACCAT CCATCACCATCACCACCAT - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88371917..88372008 26863196 MeRIP-seq:(Medium) rs1469708544 Functional Loss DEL dbSNP153 17..34 33 - - - 79160 RMVar_ID_79160 Human_SNP_ID_613611295 m1A Human chr16 + 88371959 88371957 88371960 TCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACCACCATCATCACCATCACC TCACCATCACCACCATCATCACCATCACCAC___CATCACCATCACCACCATCATCACCATCACC CCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88371917..88372008 26863196 MeRIP-seq:(Medium) rs1179798833 Functional Loss DEL dbSNP153 32..34 33 - - - 79161 RMVar_ID_79161 Human_SNP_ID_613611496 m1A Human chr16 - 88372434 88372434 88372434 TGGTAGTGATGGTGATGATGGTGATGGTGATGATGATGGTGATGATGGTGATGGTGATGATGGTG TGGTAGTGATGGTGATGATGGTGATGGTGATGTTGATGGTGATGATGGTGATGGTGATGATGGTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88372385..88372463 26863196 MeRIP-seq:(Medium) rs1399300513 Functional Loss SNV dbSNP153 33..33 33 - - - 79162 RMVar_ID_79162 Human_SNP_ID_613618536 m1A Human chr16 + 88390749 88390749 88390749 GTGTGAGGATCCTATAGTGGCTCCCTGGGGGAAGGCGTCTCTGAGCTGGGTGGGTTTTGAACGGT GTGTGAGGATCCTATAGTGGCTCCCTGGGGGAGGGCGTCTCTGAGCTGGGTGGGTTTTGAACGGT A G ZNF469 Ensembl:ENSG00000225614 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88390720..88390820 32194978 MeRIP-seq:(Medium) rs551195362 Functional Loss SNV dbSNP153 33..33 33 - - - 79163 RMVar_ID_79163 Human_SNP_ID_613622498 m1A Human chr16 + 88401535 88401532 88401535 GTGGATGGGTGAGTGGATGGATGGATGGATGCATGGGTGGATGGATGGATGCATGGGTGGATGGA GTGGATGGGTGAGTGGATGGATGGATGGAT___TGGGTGGATGGATGGATGCATGGGTGGATGGA TGCA T ZNF469 Ensembl:ENSG00000225614 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88401526..88401609 26863196 MeRIP-seq:(Medium) rs1567501585 Functional Loss DEL dbSNP153 31..33 33 - - - 79164 RMVar_ID_79164 Human_SNP_ID_613629467 m1A Human chr16 + 88422861 88422849 88422862 TGATGGATGGGTGGATGGATGGATGGATGATGATGATGGATGAGTGAATGGATGGATGGATGGAT TGATGGATGGGTGGATGGATG_____________GATGGATGAGTGAATGGATGGATGGATGGAT GGATGGATGATGAT G ZNF469 Ensembl:ENSG00000225614 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88422855..88422926 26863196 MeRIP-seq:(Medium) rs1159517143 Functional Loss DEL dbSNP153 22..34 33 - - - 79165 RMVar_ID_79165 Human_SNP_ID_613629476 m1A Human chr16 + 88422861 88422861 88422861 TGATGGATGGGTGGATGGATGGATGGATGATGATGATGGATGAGTGAATGGATGGATGGATGGAT TGATGGATGGGTGGATGGATGGATGGATGATGTTGATGGATGAGTGAATGGATGGATGGATGGAT A T ZNF469 Ensembl:ENSG00000225614 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88422855..88422926 26863196 MeRIP-seq:(Medium) rs1156444155 Functional Loss SNV dbSNP153 33..33 33 - - - 79166 RMVar_ID_79166 Human_SNP_ID_613631769 m1A Human chr16 + 88429280 88429280 88429280 TGCCGTCACCGGCCACCAACACGGCCGGCAGCACCTGCTCTTCCCTGTCGCCGATGTCCAGCAGC TGCCGTCACCGGCCACCAACACGGCCGGCAGCCCCTGCTCTTCCCTGTCGCCGATGTCCAGCAGC A C ZNF469 Ensembl:ENSG00000225614 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88429231..88429371 26863196 MeRIP-seq:(Medium) rs1330550097 Functional Loss SNV dbSNP153 33..33 33 - - - 79167 RMVar_ID_79167 Human_SNP_ID_613632550 m1A Human chr16 + 88430705 88430705 88430705 GGGCGGGCAGGTGCGGCTCCCTGGCGGCGGGGAGGCCCCGGCCCGGAGCTGAGGACCGCAGGCTC GGGCGGGCAGGTGCGGCTCCCTGGCGGCGGGGGGGCCCCGGCCCGGAGCTGAGGACCGCAGGCTC A G ZNF469 Ensembl:ENSG00000225614 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88430700..88430893 26863196 MeRIP-seq:(Medium) rs966249641 Functional Loss SNV dbSNP153 33..33 33 - - - 79168 RMVar_ID_79168 Human_SNP_ID_613634949 m1A Human chr16 + 88435982 88435982 88435982 CCCAGGGTGGAGTCCAGGGGCCTGAAGGCCCCACTCCTGATGCCTCTGGCTCCAGTGCCAAGGAT CCCAGGGTGGAGTCCAGGGGCCTGAAGGCCCCTCTCCTGATGCCTCTGGCTCCAGTGCCAAGGAT A T ZNF469 Ensembl:ENSG00000225614 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88435935..88436110 32194978 MeRIP-seq:(Medium) rs1281221958 Functional Loss SNV dbSNP153 33..33 33 - - - 79169 RMVar_ID_79169 Human_SNP_ID_613641316 m1A Human chr16 + 88453302 88453302 88453302 CCGTGCCTCCAGCCCGCCAGGAGCGCCCTCGCAGTGGCCGCCTGCTCCGCCGCTCGCCGCCCGCG CCGTGCCTCCAGCCCGCCAGGAGCGCCCTCGCGGTGGCCGCCTGCTCCGCCGCTCGCCGCCCGCG A G ZFPM1 Ensembl:ENSG00000179588 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88453298..88453452 26863196 MeRIP-seq:(Medium) rs1421751291 Functional Loss SNV dbSNP153 33..33 33 - - - 79170 RMVar_ID_79170 Human_SNP_ID_613641453 m1A Human chr16 + 88453602 88453602 88453602 CCCCCGCCGCCCGCCGCCGCCCGCCCGGGGCTAGAGGCGGCCGCCGGGAGGGCGCGCGGCGCCGG CCCCCGCCGCCCGCCGCCGCCCGCCCGGGGCTGGAGGCGGCCGCCGGGAGGGCGCGCGGCGCCGG A G ZFPM1 Ensembl:ENSG00000179588 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88453595..88453718 26863196 MeRIP-seq:(Medium) rs1214757198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393312,Human_RBP_ID_9325335,Human_RBP_ID_22712351 Human_Splice_Rec_1749035,Human_Splice_Rec_1749053,Human_Splice_Rec_1749057,Human_Splice_Rec_1749067,Human_Splice_Rec_1749073 79171 RMVar_ID_79171 Human_SNP_ID_613657023 m1A Human chr16 + 88499387 88499372 88499388 AGGAAAACAGACCTCCTCCAGAGCAGCCGCGGAGGAGAAGAGAGCAGTCGTGGGGGCCGCGCAGC AGGAAAACAGACCTCCTC________________GAGAAGAGAGCAGTCGTGGGGGCCGCGCAGC CCAGAGCAGCCGCGGAG C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88499381..88499496 26863196 MeRIP-seq:(Medium) rs1567540121 Functional Loss DEL dbSNP153 19..34 33 - - - RMVar_hsa_circ_337611 79172 RMVar_ID_79172 Human_SNP_ID_613657034 m1A Human chr16 + 88499387 88499387 88499387 AGGAAAACAGACCTCCTCCAGAGCAGCCGCGGAGGAGAAGAGAGCAGTCGTGGGGGCCGCGCAGC AGGAAAACAGACCTCCTCCAGAGCAGCCGCGGGGGAGAAGAGAGCAGTCGTGGGGGCCGCGCAGC A G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88499381..88499496 26863196 MeRIP-seq:(Medium) rs924920862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337611 79173 RMVar_ID_79173 Human_SNP_ID_613663198 m1A Human chr16 + 88517346 88517342 88517346 ATGAGTGGGTCGGTGGGTGGGTAGGTGGGTGGATGGATGGGTGGGTGGATAATGGGTGGATGATG ATGAGTGGGTCGGTGGGTGGGTAGGTGGG____TGGATGGGTGGGTGGATAATGGGTGGATGATG GTGGA G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88517339..88517651 26863196 MeRIP-seq:(Medium) rs966033056 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_261101,Human_RBP_ID_5647209,Human_RBP_ID_8185273,Human_RBP_ID_8231393,Human_RBP_ID_9419451,Human_RBP_ID_17256498,Human_RBP_ID_18939652 79174 RMVar_ID_79174 Human_SNP_ID_613663203 m1A Human chr16 - 88517351 88517351 88517351 CCACCCATCATCCACCCATTATCCACCCACCCATCCATCCACCCACCTACCCACCCACCGACCCA CCACCCATCATCCACCCATTATCCACCCACCCCTCCATCCACCCACCTACCCACCCACCGACCCA T G AC116552.1 Ensembl:ENSG00000261744 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88517343..88517449 26863196 MeRIP-seq:(Medium) rs1304683521 Functional Loss SNV dbSNP153 33..33 33 - - - 79175 RMVar_ID_79175 Human_SNP_ID_613663298 m1A Human chr16 + 88517540 88517540 88517540 ATGGATGGATGGTTGGATAGGTGGGTGGATGGATGAGTGGGTGAGTGGGTGAAGGAGGGGTGGAT ATGGATGGATGGTTGGATAGGTGGGTGGATGGGTGAGTGGGTGAGTGGGTGAAGGAGGGGTGGAT A G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88517536..88517645 26863196 MeRIP-seq:(Medium) rs1331940232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5236897,Human_RBP_ID_5289076,Human_RBP_ID_5647211,Human_RBP_ID_8185275,Human_RBP_ID_9325413,Human_RBP_ID_9419452,Human_RBP_ID_17256500,Human_RBP_ID_22523460,Human_RBP_ID_23706048 79176 RMVar_ID_79176 Human_SNP_ID_613663609 m1A Human chr16 + 88518357 88518357 88518357 GTGGATGGATGAGTGGGTGGGTGGATAGATGGATGGATGAATGAATGGGTAGGTGGCTGACAGGG GTGGATGGATGAGTGGGTGGGTGGATAGATGGGTGGATGAATGAATGGGTAGGTGGCTGACAGGG A G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88518349..88519052;chr16:88518351..88518994 26863196 MeRIP-seq:(Medium) rs1334619617 Functional Loss SNV dbSNP153 33..33 33 - - - 79177 RMVar_ID_79177 Human_SNP_ID_613663998 m1A Human chr16 + 88519165 88519165 88519165 GATGGATGGATGGATGGATGATGGGTGGATGCATGGGTGGGTGGATGGGTGGGTGGATGGGAGGG GATGGATGGATGGATGGATGATGGGTGGATGCCTGGGTGGGTGGATGGGTGGGTGGATGGGAGGG A C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88519159..88519523 26863196 MeRIP-seq:(Medium) rs1343794612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261103,Human_RBP_ID_5647223,Human_RBP_ID_8185285 79178 RMVar_ID_79178 Human_SNP_ID_613664036 m1A Human chr16 + 88519269 88519266 88519269 ATGGCTGGGTGGATGGATAGATGGATGAGTGGAGGGATGGATGGATGGATGGATGGATGGGTGGG ATGGCTGGGTGGATGGATAGATGGATGAGT___GGGATGGATGGATGGATGGATGGATGGGTGGG TGGA T ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88519264..88519365 26863196 MeRIP-seq:(Medium) rs1462767957 Functional Loss DEL dbSNP153 31..33 33 - - - 79179 RMVar_ID_79179 Human_SNP_ID_613664268 m1A Human chr16 - 88519766 88519766 88519766 ACCCACCCACCCTCCTATCCATCCATCCACCCACCATCCATCTGTCCATCTATTCATCCACCTAT ACCCACCCACCCTCCTATCCATCCATCCACCCGCCATCCATCTGTCCATCTATTCATCCACCTAT T C AC116552.1 Ensembl:ENSG00000261744 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88519763..88520059 26863196 MeRIP-seq:(Medium) rs1418373792 Functional Loss SNV dbSNP153 33..33 33 - - - 79180 RMVar_ID_79180 Human_SNP_ID_613664269 m1A Human chr16 - 88519766 88519766 88519766 ACCCACCCACCCTCCTATCCATCCATCCACCCACCATCCATCTGTCCATCTATTCATCCACCTAT ACCCACCCACCCTCCTATCCATCCATCCACCCCCCATCCATCTGTCCATCTATTCATCCACCTAT T G AC116552.1 Ensembl:ENSG00000261744 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88519763..88520059 26863196 MeRIP-seq:(Medium) rs1418373792 Functional Loss SNV dbSNP153 33..33 33 - - - 79181 RMVar_ID_79181 Human_SNP_ID_613664337 m1A Human chr16 + 88519943 88519935 88519943 CTGGGTAGATGGATAGATGGATGAGTGGATGGATGGATGAATGGATGGATGGATGGATGGATAGT CTGGGTAGATGGATAGATGGATGAG________TGGATGAATGGATGGATGGATGGATGGATAGT GTGGATGGA G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:88519907..88520036 26863196 MeRIP-seq:(Medium) rs368348204 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_23706064 79182 RMVar_ID_79182 Human_SNP_ID_613664338 m1A Human chr16 + 88519943 88519935 88519943 CTGGGTAGATGGATAGATGGATGAGTGGATGGATGGATGAATGGATGGATGGATGGATGGATAGT CTGGGTAGATGGATAGATGGATGAGTGGA____TGGATGAATGGATGGATGGATGGATGGATAGT GTGGATGGA GTGGA ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:88519907..88520036 26863196 MeRIP-seq:(Medium) rs368348204 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23706064 79183 RMVar_ID_79183 Human_SNP_ID_613665047 m1A Human chr16 - 88521480 88521480 88521480 AGGGAACATGGTGTTGGTGCTCAGGATACCTTAGCGGGGGGTCCCTGACCCACGATGGCCTGAGG AGGGAACATGGTGTTGGTGCTCAGGATACCTTGGCGGGGGGTCCCTGACCCACGATGGCCTGAGG T C AC116552.1 Ensembl:ENSG00000261744 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88521477..88521763 26863196 MeRIP-seq:(Medium) rs1038705219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5289827 79184 RMVar_ID_79184 Human_SNP_ID_613665144 m1A Human chr16 + 88521745 88521708 88521745 GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACACCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC _________________________________CCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC CCCCTGTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACA C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88521739..88522087 26863196 MeRIP-seq:(Medium) rs1319442655 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_17077715,Human_RBP_ID_18939670 79185 RMVar_ID_79185 Human_SNP_ID_613665161 m1A Human chr16 + 88521745 88521727 88521745 GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACACCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC GTGCTGTTCCCCCTC__________________CCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC CCCCTGTGCTGTTCCCACA C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88521739..88522087 26863196 MeRIP-seq:(Medium) rs1385446510 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_17077715,Human_RBP_ID_18939670 79186 RMVar_ID_79186 Human_SNP_ID_613665173 m1A Human chr16 + 88521745 88521744 88521745 GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACACCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCAC_CCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC CA C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88521739..88522087 26863196 MeRIP-seq:(Medium) rs1200808598 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17077715,Human_RBP_ID_18939670 79187 RMVar_ID_79187 Human_SNP_ID_613665175 m1A Human chr16 + 88521745 88521745 88521745 GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACACCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC GTGCTGTTCCCCCTCCCCTGTGCTGTTCCCACCCCCTGTGCTGTTCCCTCCCCTGTGCTGTTCCC A C ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88521739..88522087 26863196 MeRIP-seq:(Medium) rs1431223091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17077715,Human_RBP_ID_18939670 79188 RMVar_ID_79188 Human_SNP_ID_613665249 m1A Human chr16 - 88521872 88521872 88521872 CGAGGGGGCCAAGGAACAGCACGGGGGAGGAAACAGAGAGGAGGGAACAGCATGGAGAGGGAACA CGAGGGGGCCAAGGAACAGCACGGGGGAGGAAGCAGAGAGGAGGGAACAGCATGGAGAGGGAACA T C AC116552.1 Ensembl:ENSG00000261744 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88521870..88522121 26863196 MeRIP-seq:(Medium) rs1405884726 Functional Loss SNV dbSNP153 33..33 33 - - - 79189 RMVar_ID_79189 Human_SNP_ID_613669590 m1A Human chr16 + 88533346 88533346 88533346 CAGCGAGCCCCCGGCGGCCCCCAGGAGCATCAAGGTGGAGGCGGTGGAGGAGCCGGAGGCGGCCC CAGCGAGCCCCCGGCGGCCCCCAGGAGCATCAGGGTGGAGGCGGTGGAGGAGCCGGAGGCGGCCC A G ZFPM1 Ensembl:ENSG00000179588 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:88533340..88533539 26863410 MeRIP-seq:(Medium) rs561465555 Functional Loss SNV dbSNP153 33..33 33 - - - 79190 RMVar_ID_79190 Human_SNP_ID_613669616 m1A Human chr16 - 88533385 88533385 88533385 ACGGGGCCTGGGGCCCAGGCTCTCCGGGGCCCAGGATGGGGGCCGCCTCCGGCTCCTCCACCGCC ACGGGGCCTGGGGCCCAGGCTCTCCGGGGCCCGGGATGGGGGCCGCCTCCGGCTCCTCCACCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88533376..88533498 26863196 MeRIP-seq:(Medium) rs1287156658 Functional Loss SNV dbSNP153 33..33 33 - - - 79191 RMVar_ID_79191 Human_SNP_ID_613670031 m1A Human chr16 - 88534020 88534020 88534020 GTAGGTCTCGTGGCGGCTGAAGCGGATGTTGCAGGCCTCGCACAGCGTGCGGCTGGGGTCGTCCT GTAGGTCTCGTGGCGGCTGAAGCGGATGTTGCGGGCCTCGCACAGCGTGCGGCTGGGGTCGTCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88533513..88534135 26863196 MeRIP-seq:(Medium) rs1373310568 Functional Loss SNV dbSNP153 33..33 33 - - - 79192 RMVar_ID_79192 Human_SNP_ID_613670332 m1A Human chr16 - 88534372 88534372 88534372 AGTCGGCCAGCGCCGGTGCCGGGGCTCCGGGGAGCGGGCGCCGCGGCTTCTTGCTCAGGTCGATG AGTCGGCCAGCGCCGGTGCCGGGGCTCCGGGGGGCGGGCGCCGCGGCTTCTTGCTCAGGTCGATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88534325..88534648 26863196 MeRIP-seq:(Medium) rs768124081 Functional Loss SNV dbSNP153 33..33 33 - - - 79193 RMVar_ID_79193 Human_SNP_ID_613670333 m1A Human chr16 - 88534372 88534372 88534372 AGTCGGCCAGCGCCGGTGCCGGGGCTCCGGGGAGCGGGCGCCGCGGCTTCTTGCTCAGGTCGATG AGTCGGCCAGCGCCGGTGCCGGGGCTCCGGGGCGCGGGCGCCGCGGCTTCTTGCTCAGGTCGATG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88534325..88534648 26863196 MeRIP-seq:(Medium) rs768124081 Functional Loss SNV dbSNP153 33..33 33 - - - 79194 RMVar_ID_79194 Human_SNP_ID_613670702 m1A Human chr16 + 88534988 88534988 88534988 CACGCCGCCGAGCACGTGAAGTGAGCGCCCACACTACAGCCGCAGACGCTTTGCACGCCCCGCTG CACGCCGCCGAGCACGTGAAGTGAGCGCCCACCCTACAGCCGCAGACGCTTTGCACGCCCCGCTG A C ZFPM1 Ensembl:ENSG00000179588 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88534938..88535103 26863196 MeRIP-seq:(Medium) rs1211409036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17256512 79195 RMVar_ID_79195 Human_SNP_ID_613689893 m1A Human chr16 - 88586552 88586552 88586552 CCGTCTTAGCGTGGGGGAGGCATCTATCAATCAGCACTGCTTTCTCCAAACCAGAAGGGGCAGGA CCGTCTTAGCGTGGGGGAGGCATCTATCAATCTGCACTGCTTTCTCCAAACCAGAAGGGGCAGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88586548..88586722 26863196 MeRIP-seq:(Medium) rs1302462977 Functional Loss SNV dbSNP153 33..33 33 - - - 79196 RMVar_ID_79196 Human_SNP_ID_613689939 m1A Human chr16 + 88586678 88586678 88586678 AGGTGAGGCCTCGTCCCACCTGCCGGTTCTTCATGAAAGGTAATTGTCTGCGTGTGAGGCCTTCT AGGTGAGGCCTCGTCCCACCTGCCGGTTCTTCGTGAAAGGTAATTGTCTGCGTGTGAGGCCTTCT A G ZC3H18 Ensembl:ENSG00000158545 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88570480..88587554 32194978 MeRIP-seq:(Medium) rs763246501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890031,Human_RBP_ID_5356970,Human_RBP_ID_8812135,Human_RBP_ID_9285967,Human_RBP_ID_18686600,Human_RBP_ID_18984395,Human_RBP_ID_19075405,Human_RBP_ID_22945160,Human_RBP_ID_26329331,Human_RBP_ID_27811309 Human_Splice_Rec_1749090,Human_Splice_Rec_1749091,Human_Splice_Rec_1749124,Human_Splice_Rec_1749125,Human_Splice_Rec_1749160,Human_Splice_Rec_1749161,Human_Splice_Rec_1749167 RMVar_hsa_circ_273801,RMVar_hsa_circ_180486,RMVar_hsa_circ_315127,RMVar_hsa_circ_2886,RMVar_hsa_circ_305417,RMVar_hsa_circ_356377,RMVar_hsa_circ_289408,RMVar_hsa_circ_180487,RMVar_hsa_circ_180488 79197 RMVar_ID_79197 Human_SNP_ID_613697341 m1A Human chr16 + 88609038 88609038 88609038 TTTCAGGGTGCAGTATACAGAAACAGAGCCGTATCATAATTACCGAGTAAGTATGACTTCAATAT TTTCAGGGTGCAGTATACAGAAACAGAGCCGTGTCATAATTACCGAGTAAGTATGACTTCAATAT A G ZC3H18 Ensembl:ENSG00000158545 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88608951..88609106 26863196 MeRIP-seq:(Medium) rs1262308126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17690991,Human_RBP_ID_27811312 Human_Splice_Rec_1749099,Human_Splice_Rec_1749135,Human_Splice_Rec_1749179 RMVar_hsa_circ_180490,RMVar_hsa_circ_122783,RMVar_hsa_circ_273801,RMVar_hsa_circ_2886,RMVar_hsa_circ_289408,RMVar_hsa_circ_180487,RMVar_hsa_circ_180488,RMVar_hsa_circ_291616,RMVar_hsa_circ_296887,RMVar_hsa_circ_268427,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_180491,RMVar_hsa_circ_180496,RMVar_hsa_circ_368871,RMVar_hsa_circ_325079,RMVar_hsa_circ_180494,RMVar_hsa_circ_295469,RMVar_hsa_circ_180497,RMVar_hsa_circ_180495,RMVar_hsa_circ_276036 79198 RMVar_ID_79198 Human_SNP_ID_613702320 m1A Human chr16 + 88623343 88623343 88623343 CCAGACACAGCTCGTTCTCAGGAAGCCGGTCCAGGTATGTCCCCAGGGCCCATGAAGGGCCCTCA CCAGACACAGCTCGTTCTCAGGAAGCCGGTCCCGGTATGTCCCCAGGGCCCATGAAGGGCCCTCA A C ZC3H18 Ensembl:ENSG00000158545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:88623226..88623566;chr16:88623177..88623566 26863196 MeRIP-seq:(Medium) rs757803844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19072306 Human_Splice_Rec_1749105,Human_Splice_Rec_1749141,Human_Splice_Rec_1749183 RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_73935,RMVar_hsa_circ_45728 79199 RMVar_ID_79199 Human_SNP_ID_613702586 m1A Human chr16 - 88624064 88624064 88624064 CCGGCCAGGACTTGCCCACAGGCTGGGCACTCACCCTGCTTTCCCGGGCGGCGGGGCCGGCTCTC CCGGCCAGGACTTGCCCACAGGCTGGGCACTCGCCCTGCTTTCCCGGGCGGCGGGGCCGGCTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88623928..88624116;chr16:88623919..88624116 26863196 MeRIP-seq:(Medium) rs1159648007 Functional Loss SNV dbSNP153 33..33 33 - - - 79200 RMVar_ID_79200 Human_SNP_ID_613702752 m1A Human chr16 + 88624545 88624545 88624545 CCCCGAGCTGTGGGTCCATTGAAAGGGGATGTAGGCCAGCGGGGCCCCGTCCACCAGCCCTGCCC CCCCGAGCTGTGGGTCCATTGAAAGGGGATGTGGGCCAGCGGGGCCCCGTCCACCAGCCCTGCCC A G ZC3H18 Ensembl:ENSG00000158545 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88624544..88624750 26863196 MeRIP-seq:(Medium) rs527586882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24370036 GWAS_ID_9532 RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_73935,RMVar_hsa_circ_45728 79201 RMVar_ID_79201 Human_SNP_ID_613702765 m1A Human chr16 + 88624565 88624565 88624565 GAAAGGGGATGTAGGCCAGCGGGGCCCCGTCCACCAGCCCTGCCCTGCTCGAGCCTCCCTGTCTC GAAAGGGGATGTAGGCCAGCGGGGCCCCGTCCTCCAGCCCTGCCCTGCTCGAGCCTCCCTGTCTC A T ZC3H18 Ensembl:ENSG00000158545 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88624562..88624725 26863196 MeRIP-seq:(Medium) rs531991427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889045,Human_RBP_ID_22541912,Human_RBP_ID_24370036,Human_RBP_ID_26780890 RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_73935,RMVar_hsa_circ_45728 79202 RMVar_ID_79202 Human_SNP_ID_613702811 m1A Human chr16 + 88624651 88624651 88624651 AGCCGGCCCCGCCTCCAGCCCCACCACAGGCCACCAAAACCACTGCTCCTGTCCCCGAGCCCACC AGCCGGCCCCGCCTCCAGCCCCACCACAGGCCGCCAAAACCACTGCTCCTGTCCCCGAGCCCACC A G ZC3H18 Ensembl:ENSG00000158545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:88624564..88625371;chr16:88624557..88624741 26863196 MeRIP-seq:(Medium) rs767661703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890794,Human_RBP_ID_5114004,Human_RBP_ID_5361121 Human_Splice_Rec_1749108,Human_Splice_Rec_1749109,Human_Splice_Rec_1749144,Human_Splice_Rec_1749145,Human_Splice_Rec_1749185,Human_Splice_Rec_1749188,Human_Splice_Rec_1749189,Human_Splice_Rec_1749193 RMVar_hsa_circ_306,RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_73935,RMVar_hsa_circ_45728 79203 RMVar_ID_79203 Human_SNP_ID_613703820 m1A Human chr16 + 88627483 88627483 88627483 ACGTCCCTTACTTTGTAACCCTGAAACTGCCCAGTGTCCCCCCAAAATCACACATTCCGTGGGTA ACGTCCCTTACTTTGTAACCCTGAAACTGCCCGGTGTCCCCCCAAAATCACACATTCCGTGGGTA A G ZC3H18 Ensembl:ENSG00000158545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88627482..88627583 26863196 MeRIP-seq:(Medium) rs969095981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12844108 RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_45728,RMVar_hsa_circ_351933 79204 RMVar_ID_79204 Human_SNP_ID_613705283 m1A Human chr16 + 88631159 88631159 88631159 AGAGCTCCAGCAAGGTCACGAGCGTGCCCGGCAAAGCCTCGGATCCCGGCGCCGCCAGCACCAAA AGAGCTCCAGCAAGGTCACGAGCGTGCCCGGCGAAGCCTCGGATCCCGGCGCCGCCAGCACCAAA A G ZC3H18 Ensembl:ENSG00000158545 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:88631151..88631323 26863196 MeRIP-seq:(Medium) rs761312390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26811644 Human_Splice_Rec_1749120,Human_Splice_Rec_1749156,Human_Splice_Rec_1749202,Human_Splice_Rec_1749208,Human_Splice_Rec_1749214,Human_Splice_Rec_1749216 79205 RMVar_ID_79205 Human_SNP_ID_613705439 m1A Human chr16 + 88631559 88631559 88631559 TAGTGACCAGCACGGTTCTCATGTAAATTACAAGCCCCAGCCGCCAGCCCCGCCTTCTCTTCCTC TAGTGACCAGCACGGTTCTCATGTAAATTACAGGCCCCAGCCGCCAGCCCCGCCTTCTCTTCCTC A G ZC3H18 Ensembl:ENSG00000158545 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88631374..88631708 26863196 MeRIP-seq:(Medium) rs944738001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5114006,Human_RBP_ID_17653612,Human_RBP_ID_18940789,Human_RBP_ID_21889002 Human_Splice_Rec_1749210 79206 RMVar_ID_79206 Human_SNP_ID_613711311 m1A Human chr16 - 88646119 88646119 88646119 GCCTGCCTGGCCATTGCGAGCGGCATCTACCTACTGGTGAGTGGCGCCCTCTGAGGTCGGCCCCG GCCTGCCTGGCCATTGCGAGCGGCATCTACCTGCTGGTGAGTGGCGCCCTCTGAGGTCGGCCCCG T C CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88646101..88646125 26863196 MeRIP-seq:(Medium) rs1187214764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760447,Human_RBP_ID_5114356,Human_RBP_ID_9326255,Human_RBP_ID_22441643,Human_RBP_ID_22759918 Human_Splice_Rec_1749230,Human_Splice_Rec_1749231,Human_Splice_Rec_1749234,Human_Splice_Rec_1749235,Human_Splice_Rec_1749243,Human_Splice_Rec_1749252,Human_Splice_Rec_1749253,Human_Splice_Rec_1749262,Human_Splice_Rec_1749263,Human_Splice_Rec_1749272,Human_Splice_Rec_1749288,Human_Splice_Rec_1749294 RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_93560,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_180501,RMVar_hsa_circ_296313 79207 RMVar_ID_79207 Human_SNP_ID_613711341 m1A Human chr16 - 88646166 88646166 88646166 GGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCCACCATCCTTGGGACCGCCTGCCTGGCCATTGCG GGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCCGCCATCCTTGGGACCGCCTGCCTGGCCATTGCG T C CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88646076..88646242 26863196 MeRIP-seq:(Medium) rs780561341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895601,Human_RBP_ID_4388926,Human_RBP_ID_5142044,Human_RBP_ID_9326255,Human_RBP_ID_22441162,Human_RBP_ID_22759920 Human_Splice_Rec_1749230,Human_Splice_Rec_1749231,Human_Splice_Rec_1749234,Human_Splice_Rec_1749235,Human_Splice_Rec_1749243,Human_Splice_Rec_1749252,Human_Splice_Rec_1749253,Human_Splice_Rec_1749262,Human_Splice_Rec_1749263,Human_Splice_Rec_1749272,Human_Splice_Rec_1749288,Human_Splice_Rec_1749294 Human_miRNA_ID_1957515 RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_93560,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_180501,RMVar_hsa_circ_296313 79208 RMVar_ID_79208 Human_SNP_ID_613711351 m1A Human chr16 - 88646199 88646184 88646200 TCTGTGTCCCTGCCTCTCACCCGCTGTCCCCCAGGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCC TCTGTGTCCCTGCCTCTCACCCGCTGTCCCC________________GCCGGCTTCCTGCTGGCC CGGGCACCGAGAGCCTG C CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:88646084..88646227;chr16:88646101..88646200;chr16:88646101..88646269 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1567608830 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_9326255,Human_RBP_ID_19075420,Human_RBP_ID_22441162,Human_RBP_ID_22652514 Human_Splice_Rec_1749231,Human_Splice_Rec_1749235,Human_Splice_Rec_1749243,Human_Splice_Rec_1749253,Human_Splice_Rec_1749263 RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313 79209 RMVar_ID_79209 Human_SNP_ID_613711368 m1A Human chr16 - 88646199 88646199 88646199 TCTGTGTCCCTGCCTCTCACCCGCTGTCCCCCAGGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCC TCTGTGTCCCTGCCTCTCACCCGCTGTCCCCCTGGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCC T A CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:88646084..88646227;chr16:88646101..88646200;chr16:88646101..88646269 26863196,32194978,32194978 MeRIP-seq:(Medium) rs112145460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326255,Human_RBP_ID_19075420,Human_RBP_ID_22441162,Human_RBP_ID_22652514 Human_Splice_Rec_1749231,Human_Splice_Rec_1749235,Human_Splice_Rec_1749243,Human_Splice_Rec_1749253,Human_Splice_Rec_1749263 RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313 79210 RMVar_ID_79210 Human_SNP_ID_613711369 m1A Human chr16 - 88646199 88646199 88646199 TCTGTGTCCCTGCCTCTCACCCGCTGTCCCCCAGGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCC TCTGTGTCCCTGCCTCTCACCCGCTGTCCCCCCGGCTCTCGGTGCCCGCCGGCTTCCTGCTGGCC T G CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:88646084..88646227;chr16:88646101..88646200;chr16:88646101..88646269 26863196,32194978,32194978 MeRIP-seq:(Medium) rs112145460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326255,Human_RBP_ID_19075420,Human_RBP_ID_22441162,Human_RBP_ID_22652514 Human_Splice_Rec_1749231,Human_Splice_Rec_1749235,Human_Splice_Rec_1749243,Human_Splice_Rec_1749253,Human_Splice_Rec_1749263 RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313 79211 RMVar_ID_79211 Human_SNP_ID_613711675 m1A Human chr16 - 88646833 88646833 88646833 GCCGTCTCGCCTTCCTCCCTCCCCCAGGGGACAGAAGTACATGACCGCCGTGGTGAAGCTGTTCG GCCGTCTCGCCTTCCTCCCTCCCCCAGGGGACGGAAGTACATGACCGCCGTGGTGAAGCTGTTCG T C CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88646724..88646879 26863196 MeRIP-seq:(Medium) rs774641186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760448,Human_RBP_ID_890796,Human_RBP_ID_5361131,Human_RBP_ID_9340931,Human_RBP_ID_17653130,Human_RBP_ID_19072312,Human_RBP_ID_22415807,Human_RBP_ID_22441163,Human_RBP_ID_22759922,Human_RBP_ID_24531691 Human_Splice_Rec_1749228,Human_Splice_Rec_1749229,Human_Splice_Rec_1749233,Human_Splice_Rec_1749242,Human_Splice_Rec_1749250,Human_Splice_Rec_1749251,Human_Splice_Rec_1749260,Human_Splice_Rec_1749261,Human_Splice_Rec_1749270,Human_Splice_Rec_1749271,Human_Splice_Rec_1749278,Human_Splice_Rec_1749284,Human_Splice_Rec_1749285,Human_Splice_Rec_1749293 RMVar_hsa_circ_79126,RMVar_hsa_circ_180502,RMVar_hsa_circ_85882,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_84962,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_180506,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79212 RMVar_ID_79212 Human_SNP_ID_613711680 m1A Human chr16 - 88646840 88646840 88646840 CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCAGGGGACAGAAGTACATGACCGCCGTGGTGAAG CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCTGGGGACAGAAGTACATGACCGCCGTGGTGAAG T A CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88646826..88646850 26863196 MeRIP-seq:(Medium) rs113932941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890796,Human_RBP_ID_5361131,Human_RBP_ID_19072312,Human_RBP_ID_22415807,Human_RBP_ID_22441163 Human_Splice_Rec_1749229,Human_Splice_Rec_1749233,Human_Splice_Rec_1749251,Human_Splice_Rec_1749261,Human_Splice_Rec_1749271,Human_Splice_Rec_1749285,Human_Splice_Rec_1749293 RMVar_hsa_circ_79126,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79213 RMVar_ID_79213 Human_SNP_ID_613711681 m1A Human chr16 - 88646840 88646840 88646840 CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCAGGGGACAGAAGTACATGACCGCCGTGGTGAAG CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCGGGGGACAGAAGTACATGACCGCCGTGGTGAAG T C CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88646826..88646850 26863196 MeRIP-seq:(Medium) rs113932941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890796,Human_RBP_ID_5361131,Human_RBP_ID_19072312,Human_RBP_ID_22415807,Human_RBP_ID_22441163 Human_Splice_Rec_1749229,Human_Splice_Rec_1749233,Human_Splice_Rec_1749251,Human_Splice_Rec_1749261,Human_Splice_Rec_1749271,Human_Splice_Rec_1749285,Human_Splice_Rec_1749293 RMVar_hsa_circ_79126,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79214 RMVar_ID_79214 Human_SNP_ID_613711682 m1A Human chr16 - 88646840 88646840 88646840 CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCAGGGGACAGAAGTACATGACCGCCGTGGTGAAG CAGCCGCGCCGTCTCGCCTTCCTCCCTCCCCCCGGGGACAGAAGTACATGACCGCCGTGGTGAAG T G CYBA Ensembl:ENSG00000051523 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88646826..88646850 26863196 MeRIP-seq:(Medium) rs113932941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890796,Human_RBP_ID_5361131,Human_RBP_ID_19072312,Human_RBP_ID_22415807,Human_RBP_ID_22441163 Human_Splice_Rec_1749229,Human_Splice_Rec_1749233,Human_Splice_Rec_1749251,Human_Splice_Rec_1749261,Human_Splice_Rec_1749271,Human_Splice_Rec_1749285,Human_Splice_Rec_1749293 RMVar_hsa_circ_79126,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79215 RMVar_ID_79215 Human_SNP_ID_613711836 m1A Human chr16 - 88647146 88647146 88647146 CAGTGTGGCGGGCGTGTTTGTGTGCCTGCTGGAGTACCCCCGGGGGAAGAGGAAGAAGGGCTCCA CAGTGTGGCGGGCGTGTTTGTGTGCCTGCTGGTGTACCCCCGGGGGAAGAGGAAGAAGGGCTCCA T A CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88647126..88647150 26863196 MeRIP-seq:(Medium) rs179363893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760449,Human_RBP_ID_895556,Human_RBP_ID_4393315,Human_RBP_ID_5113690,Human_RBP_ID_5316926,Human_RBP_ID_8441799,Human_RBP_ID_9325438,Human_RBP_ID_9340933,Human_RBP_ID_17653617,Human_RBP_ID_22441164,Human_RBP_ID_22739818,Human_RBP_ID_22759924,Human_RBP_ID_23706172 Human_Splice_Rec_1749226,Human_Splice_Rec_1749227,Human_Splice_Rec_1749240,Human_Splice_Rec_1749241,Human_Splice_Rec_1749248,Human_Splice_Rec_1749249,Human_Splice_Rec_1749258,Human_Splice_Rec_1749259,Human_Splice_Rec_1749268,Human_Splice_Rec_1749269,Human_Splice_Rec_1749276,Human_Splice_Rec_1749277,Human_Splice_Rec_1749282,Human_Splice_Rec_1749283,Human_Splice_Rec_1749292 GWAS_ID_9533 RMVar_hsa_circ_79126,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79216 RMVar_ID_79216 Human_SNP_ID_613711837 m1A Human chr16 - 88647146 88647146 88647146 CAGTGTGGCGGGCGTGTTTGTGTGCCTGCTGGAGTACCCCCGGGGGAAGAGGAAGAAGGGCTCCA CAGTGTGGCGGGCGTGTTTGTGTGCCTGCTGGGGTACCCCCGGGGGAAGAGGAAGAAGGGCTCCA T C CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88647126..88647150 26863196 MeRIP-seq:(Medium) rs179363893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760449,Human_RBP_ID_895556,Human_RBP_ID_4393315,Human_RBP_ID_5113690,Human_RBP_ID_5316926,Human_RBP_ID_8441799,Human_RBP_ID_9325438,Human_RBP_ID_9340933,Human_RBP_ID_17653617,Human_RBP_ID_22441164,Human_RBP_ID_22739818,Human_RBP_ID_22759924,Human_RBP_ID_23706172 Human_Splice_Rec_1749226,Human_Splice_Rec_1749227,Human_Splice_Rec_1749240,Human_Splice_Rec_1749241,Human_Splice_Rec_1749248,Human_Splice_Rec_1749249,Human_Splice_Rec_1749258,Human_Splice_Rec_1749259,Human_Splice_Rec_1749268,Human_Splice_Rec_1749269,Human_Splice_Rec_1749276,Human_Splice_Rec_1749277,Human_Splice_Rec_1749282,Human_Splice_Rec_1749283,Human_Splice_Rec_1749292 GWAS_ID_9533 RMVar_hsa_circ_79126,RMVar_hsa_circ_83204,RMVar_hsa_circ_180503,RMVar_hsa_circ_296313,RMVar_hsa_circ_82112,RMVar_hsa_circ_180504,RMVar_hsa_circ_180505,RMVar_hsa_circ_82350,RMVar_hsa_circ_180507 79217 RMVar_ID_79217 Human_SNP_ID_613712153 m1A Human chr16 + 88648096 88648095 88648096 ACCACTGGGTGAAGCGCCCAGCTGTGGCCACGATGCCCCCGGTGATGAGGACTGCGGGGAGAAGT ACCACTGGGTGAAGCGCCCAGCTGTGGCCACG_TGCCCCCGGTGATGAGGACTGCGGGGAGAAGT GA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88648027..88651004 32194978 MeRIP-seq:(Medium) rs1326361967 Functional Loss DEL dbSNP153 33..33 33 - - - 79218 RMVar_ID_79218 Human_SNP_ID_613713387 m1A Human chr16 + 88650998 88650998 88650998 CGCCAGCGCCTGTTCGTTGGCCCACATGGCCCACTCGATCTGCCCCATGGCGACACGAACCCGGC CGCCAGCGCCTGTTCGTTGGCCCACATGGCCCGCTCGATCTGCCCCATGGCGACACGAACCCGGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:88650951..88651050 26863196 MeRIP-seq:(Medium) rs1247337146 Functional Loss SNV dbSNP153 33..33 33 - - - 79219 RMVar_ID_79219 Human_SNP_ID_613714806 m1A Human chr16 - 88654779 88654779 88654779 CCAGGTGGCGTACACCTTTGACGCGGGCCCCAATGCCGTGATCTTCACCCTGGACGACACTGTGG CCAGGTGGCGTACACCTTTGACGCGGGCCCCAGTGCCGTGATCTTCACCCTGGACGACACTGTGG T C MVD Ensembl:ENSG00000167508 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88654728..88655879 32194978 MeRIP-seq:(Medium) rs780751762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481509,Human_RBP_ID_17652763,Human_RBP_ID_17882500,Human_RBP_ID_18984402 Human_Splice_Rec_1749302,Human_Splice_Rec_1749303,Human_Splice_Rec_1749320,Human_Splice_Rec_1749321,Human_Splice_Rec_1749327 RMVar_hsa_circ_123219,RMVar_hsa_circ_88589,RMVar_hsa_circ_94572,RMVar_hsa_circ_180509,RMVar_hsa_circ_180511,RMVar_hsa_circ_78363,RMVar_hsa_circ_180510,RMVar_hsa_circ_180508 79220 RMVar_ID_79220 Human_SNP_ID_613716256 m1A Human chr16 + 88658028 88658028 88658028 CCTTGCTGATGACGGCTGTTGTGGTGGTTTTTAACTGAAAAGGAAACCCAGGGCCACCTCAGAGG CCTTGCTGATGACGGCTGTTGTGGTGGTTTTTCACTGAAAAGGAAACCCAGGGCCACCTCAGAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88657882..88658058 26863196 MeRIP-seq:(Medium) rs752585992 Functional Loss SNV dbSNP153 33..33 33 - - - 79221 RMVar_ID_79221 Human_SNP_ID_613716257 m1A Human chr16 + 88658028 88658028 88658028 CCTTGCTGATGACGGCTGTTGTGGTGGTTTTTAACTGAAAAGGAAACCCAGGGCCACCTCAGAGG CCTTGCTGATGACGGCTGTTGTGGTGGTTTTTTACTGAAAAGGAAACCCAGGGCCACCTCAGAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88657882..88658058 26863196 MeRIP-seq:(Medium) rs752585992 Functional Loss SNV dbSNP153 33..33 33 - - - 79222 RMVar_ID_79222 Human_SNP_ID_613716509 m1A Human chr16 - 88658722 88658722 88658722 AGCCCACCGGCCTGGCCCTGGCTGTTCATTACAGGGGGCAAGCGCGATGAAGAGCTGGTTCTGCC AGCCCACCGGCCTGGCCCTGGCTGTTCATTACCGGGGGCAAGCGCGATGAAGAGCTGGTTCTGCC T G MVD Ensembl:ENSG00000167508 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:88658651..88658750 26863410 MeRIP-seq:(Medium) rs112140447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199522,Human_RBP_ID_892797,Human_RBP_ID_3503298,Human_RBP_ID_3948056,Human_RBP_ID_5317906,Human_RBP_ID_5361151,Human_RBP_ID_8087638,Human_RBP_ID_9419459,Human_RBP_ID_12844278,Human_RBP_ID_19072334,Human_RBP_ID_21972743,Human_RBP_ID_22541926,Human_RBP_ID_22654617 Human_Splice_Rec_1749309,Human_Splice_Rec_1749333,Human_Splice_Rec_1749349,Human_Splice_Rec_1749359,Human_Splice_Rec_1749369,Human_Splice_Rec_1749377,Human_Splice_Rec_1749385,Human_Splice_Rec_1749389,Human_Splice_Rec_1749401,Human_Splice_Rec_1749409 RMVar_hsa_circ_94572,RMVar_hsa_circ_180511,RMVar_hsa_circ_99166,RMVar_hsa_circ_180514,RMVar_hsa_circ_180518,RMVar_hsa_circ_180519 79223 RMVar_ID_79223 Human_SNP_ID_613716570 m1A Human chr16 - 88658859 88658856 88658859 GCAGTTCTTGCAGGCCGGGGTCTGGCAGGAGGAGGGGCACACAGGTTGTGCGGTGAGAGACGGGA GCAGTTCTTGCAGGCCGGGGTCTGGCAGGAGG___GGCACACAGGTTGTGCGGTGAGAGACGGGA CCCT C MVD Ensembl:ENSG00000167508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88658855..88659032 26863196 MeRIP-seq:(Medium) rs1371890125 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3509508,Human_RBP_ID_5113696,Human_RBP_ID_5182038,Human_RBP_ID_8185322,Human_RBP_ID_9419460,Human_RBP_ID_22541927 RMVar_hsa_circ_94572,RMVar_hsa_circ_180511,RMVar_hsa_circ_99166,RMVar_hsa_circ_180514,RMVar_hsa_circ_180518,RMVar_hsa_circ_180519 79224 RMVar_ID_79224 Human_SNP_ID_613717998 m1A Human chr16 + 88663045 88663045 88663045 TACTTGATGACCGCGATGTTGACCGGCGCTGTACAAGTGACTGCCGCCAGCGGCTTCTCCGAGGC TACTTGATGACCGCGATGTTGACCGGCGCTGTGCAAGTGACTGCCGCCAGCGGCTTCTCCGAGGC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:88663024..88663108 26863410 MeRIP-seq:(Medium) rs777732805 Functional Loss SNV dbSNP153 33..33 33 - - - 79225 RMVar_ID_79225 Human_SNP_ID_613718013 m1A Human chr16 + 88663061 88663061 88663061 TGTTGACCGGCGCTGTACAAGTGACTGCCGCCAGCGGCTTCTCCGAGGCCATGGTCCCACCGCGC TGTTGACCGGCGCTGTACAAGTGACTGCCGCCGGCGGCTTCTCCGAGGCCATGGTCCCACCGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:88662911..88663150;chr16:88662949..88663104;chr16:88662790..88663150;chr16:88662943..88663150 26863196 MeRIP-seq:(Medium) rs1567619842 Functional Loss SNV dbSNP153 33..33 33 - - - 79226 RMVar_ID_79226 Human_SNP_ID_613721320 m1A Human chr16 - 88671851 88671851 88671851 ACACGGAGGAAAGATGGCAGCACTGTGAGAACACGGACCTGGGTCTTGGCAGGAATGAGGTGAGC ACACGGAGGAAAGATGGCAGCACTGTGAGAACGCGGACCTGGGTCTTGGCAGGAATGAGGTGAGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:88671824..88671953 26863196 MeRIP-seq:(Medium) rs1443677505 Functional Loss SNV dbSNP153 33..33 33 - - - 79227 RMVar_ID_79227 Human_SNP_ID_613730303 m1A Human chr16 + 88697540 88697540 88697540 TGCGACACAGGAGCGGGGACATCCCTGACCCCAGACGCAGGCGGGTGGCTGCGCTTCCCTTCAGT TGCGACACAGGAGCGGGGACATCCCTGACCCCGGACGCAGGCGGGTGGCTGCGCTTCCCTTCAGT A G AC138028.3 Ensembl:ENSG00000259813 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:88697442..88697543 26863410 MeRIP-seq:(Medium) rs775484839 Functional Loss SNV dbSNP153 33..33 33 - - - 79228 RMVar_ID_79228 Human_SNP_ID_613730334 m1A Human chr16 + 88697593 88697593 88697593 CTTCCCTTCAGTTCTCAGAGAGAGACAGGGCCAGAGCAGCCTGGAAGGCGGCCTCCTCGTCAATA CTTCCCTTCAGTTCTCAGAGAGAGACAGGGCCGGAGCAGCCTGGAAGGCGGCCTCCTCGTCAATA A G AC138028.3 Ensembl:ENSG00000259813 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88697542..88697693 32194978 MeRIP-seq:(Medium) rs1341190526 Functional Loss SNV dbSNP153 33..33 33 - - - 79229 RMVar_ID_79229 Human_SNP_ID_613731926 m1A Human chr16 + 88701249 88701249 88701249 CCATCAAGTGACCCCGGCTCCAGGGCGGCCCAAGCAGGCGGGTACCTTTTTGTTGCAGCCTCGAC CCATCAAGTGACCCCGGCTCCAGGGCGGCCCAGGCAGGCGGGTACCTTTTTGTTGCAGCCTCGAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88701244..88701346 26863196 MeRIP-seq:(Medium) rs764766797 Functional Loss SNV dbSNP153 33..33 33 - - - 79230 RMVar_ID_79230 Human_SNP_ID_613734285 m1A Human chr16 + 88706571 88706556 88706571 GGTGGGCGAGGACTACGGGGAGCCGGCGCCTGAGGAGCCGCCCCCGGCGCCGCGGCCCAGGTAAG GGTGGGCGAGGACTACGG_______________GGAGCCGCCCCCGGCGCCGCGGCCCAGGTAAG GGGAGCCGGCGCCTGA G CTU2 Ensembl:ENSG00000174177 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88706544..88706628 26863196 MeRIP-seq:(Medium) rs1321249671 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_4389095,Human_RBP_ID_9285970,Human_RBP_ID_22442694 Human_Splice_Rec_1749545,Human_Splice_Rec_1749571,Human_Splice_Rec_1749597,Human_Splice_Rec_1749625,Human_Splice_Rec_1749653 RMVar_hsa_circ_79830,RMVar_hsa_circ_180529 79231 RMVar_ID_79231 Human_SNP_ID_613734554 m1A Human chr16 + 88707097 88707097 88707097 CCCCAAAGCCCACTAGGCGTGGGGAAGATGTGATCTGTGTTTCTCTCTTCTCCCCCCTCCCATCT CCCCAAAGCCCACTAGGCGTGGGGAAGATGTGTTCTGTGTTTCTCTCTTCTCCCCCCTCCCATCT A T CTU2 Ensembl:ENSG00000174177 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88707094..88707225 26863196 MeRIP-seq:(Medium) rs1242130611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79830,RMVar_hsa_circ_180529 79232 RMVar_ID_79232 Human_SNP_ID_613736277 m1A Human chr16 + 88710799 88710799 88710799 AGGGAAGATTGGGAAAGGGGCGGGGGTTTGCCAGGAGAAGCAAAGGGAGCAGCGTTTGAGGTGGA AGGGAAGATTGGGAAAGGGGCGGGGGTTTGCCTGGAGAAGCAAAGGGAGCAGCGTTTGAGGTGGA A T CTU2 Ensembl:ENSG00000174177 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88710790..88711110 26863196 MeRIP-seq:(Medium) rs1282233584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5356106 RMVar_hsa_circ_79830,RMVar_hsa_circ_180529 79233 RMVar_ID_79233 Human_SNP_ID_613737329 m1A Human chr16 - 88712652 88712652 88712652 CCCCTCGGATCCCACCAGCTCCTGGGCAGAGCACCAAAGCACCGACGGTGGCAGGCTGAACACCT CCCCTCGGATCCCACCAGCTCCTGGGCAGAGCTCCAAAGCACCGACGGTGGCAGGCTGAACACCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88712276..88712764 26863196 MeRIP-seq:(Medium) rs768075874 Functional Loss SNV dbSNP153 33..33 33 - - - 79234 RMVar_ID_79234 Human_SNP_ID_613737330 m1A Human chr16 - 88712652 88712652 88712652 CCCCTCGGATCCCACCAGCTCCTGGGCAGAGCACCAAAGCACCGACGGTGGCAGGCTGAACACCT CCCCTCGGATCCCACCAGCTCCTGGGCAGAGCGCCAAAGCACCGACGGTGGCAGGCTGAACACCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88712276..88712764 26863196 MeRIP-seq:(Medium) rs768075874 Functional Loss SNV dbSNP153 33..33 33 - - - 79235 RMVar_ID_79235 Human_SNP_ID_613737437 m1A Human chr16 + 88712800 88712800 88712800 GGAACAGCCACCCCAGCCCCCGCTGGACCCCCAGAACCTGGCAAGACCGCCTGCCCCTGCCCAGA GGAACAGCCACCCCAGCCCCCGCTGGACCCCCGGAACCTGGCAAGACCGCCTGCCCCTGCCCAGA A G CTU2 Ensembl:ENSG00000174177 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88712750..88712898 26863196 MeRIP-seq:(Medium) rs760061492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8812140 RMVar_hsa_circ_79830,RMVar_hsa_circ_180529 79236 RMVar_ID_79236 Human_SNP_ID_613737697 m1A Human chr16 - 88713223 88713223 88713223 TCTCGGGTATGAGTGGGGGTCAGGGCCCGGGGAAGGGGGGCTCTCAGGGGTATGAGTGGGGGTCA TCTCGGGTATGAGTGGGGGTCAGGGCCCGGGGGAGGGGGGCTCTCAGGGGTATGAGTGGGGGTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88712839..88714156 26863196 MeRIP-seq:(Medium) rs1481247446 Functional Loss SNV dbSNP153 33..33 33 - - - 79237 RMVar_ID_79237 Human_SNP_ID_613738680 m1A Human chr16 + 88714459 88714459 88714459 CTGGCGACTCCGGCCCCCGCTGCCTCCTCTGCATGTGTGCCCTGGACGTCGACGCCGCTGGTCTG CTGGCGACTCCGGCCCCCGCTGCCTCCTCTGCGTGTGTGCCCTGGACGTCGACGCCGCTGGTCTG A G CTU2 Ensembl:ENSG00000174177 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88714408..88714559 26863196 MeRIP-seq:(Medium) rs1165393976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1749562,Human_Splice_Rec_1749563,Human_Splice_Rec_1749590,Human_Splice_Rec_1749591,Human_Splice_Rec_1749616,Human_Splice_Rec_1749617,Human_Splice_Rec_1749644,Human_Splice_Rec_1749645,Human_Splice_Rec_1749682,Human_Splice_Rec_1749692,Human_Splice_Rec_1749693 79238 RMVar_ID_79238 Human_SNP_ID_613739721 m1A Human chr16 - 88715690 88715690 88715690 CATCTTCCTGGTGCGGGAGACTCGGGAGCTGGAGCTGGAGGAGGAGTTGTACGCCAAGCTCATCT CATCTTCCTGGTGCGGGAGACTCGGGAGCTGGTGCTGGAGGAGGAGTTGTACGCCAAGCTCATCT T A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88715641..88716068 32194978 MeRIP-seq:(Medium) rs914014470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6545462,Human_RBP_ID_8811035,Human_RBP_ID_9285972,Human_RBP_ID_22053556,Human_RBP_ID_22498558,Human_RBP_ID_22944716,Human_RBP_ID_23209471 RMVar_hsa_circ_91942,RMVar_hsa_circ_180531 79239 RMVar_ID_79239 Human_SNP_ID_613739722 m1A Human chr16 - 88715690 88715690 88715690 CATCTTCCTGGTGCGGGAGACTCGGGAGCTGGAGCTGGAGGAGGAGTTGTACGCCAAGCTCATCT CATCTTCCTGGTGCGGGAGACTCGGGAGCTGGGGCTGGAGGAGGAGTTGTACGCCAAGCTCATCT T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88715641..88716068 32194978 MeRIP-seq:(Medium) rs914014470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6545462,Human_RBP_ID_8811035,Human_RBP_ID_9285972,Human_RBP_ID_22053556,Human_RBP_ID_22498558,Human_RBP_ID_22944716,Human_RBP_ID_23209471 RMVar_hsa_circ_91942,RMVar_hsa_circ_180531 79240 RMVar_ID_79240 Human_SNP_ID_613740001 m1A Human chr16 - 88716074 88716074 88716074 CTACCTCGGCGTGCGTATCCAGCTGCGGAGGGAGCAGGGTGCGGGGGCCACCGGCTTCCTCGAAT CTACCTCGGCGTGCGTATCCAGCTGCGGAGGGGGCAGGGTGCGGGGGCCACCGGCTTCCTCGAAT T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:88716026..88716100;chr16:88716026..88716075 26863196 MeRIP-seq:(Medium) rs1162591534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5142060,Human_RBP_ID_5356990,Human_RBP_ID_22442269,Human_RBP_ID_22532849,Human_RBP_ID_27811314 Human_Splice_Rec_1749800,Human_Splice_Rec_1749818,Human_Splice_Rec_1749822,Human_Splice_Rec_1749836,Human_Splice_Rec_1749852,Human_Splice_Rec_1749860 RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_126808,RMVar_hsa_circ_180531,RMVar_hsa_circ_180532,RMVar_hsa_circ_180533 79241 RMVar_ID_79241 Human_SNP_ID_613740106 m1A Human chr16 - 88716226 88716226 88716226 CCCAAGTACATCCGTGCCCCCAACGGGCCCGAAGCCAACCCTGTGAAGCAGCTGCAGCCCAGTGA CCCAAGTACATCCGTGCCCCCAACGGGCCCGAGGCCAACCCTGTGAAGCAGCTGCAGCCCAGTGA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr16:88715976..88716277;chr16:88716201..88716225 26863196 MeRIP-seq:(Medium) rs1452722714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481558,Human_RBP_ID_2489507,Human_RBP_ID_3949676,Human_RBP_ID_5356992,Human_RBP_ID_5465759,Human_RBP_ID_8812142,Human_RBP_ID_26328251 Human_Splice_Rec_1749798,Human_Splice_Rec_1749799,Human_Splice_Rec_1749816,Human_Splice_Rec_1749817,Human_Splice_Rec_1749821,Human_Splice_Rec_1749834,Human_Splice_Rec_1749835,Human_Splice_Rec_1749850,Human_Splice_Rec_1749851,Human_Splice_Rec_1749858,Human_Splice_Rec_1749859 Human_miRNA_ID_2294359,Human_miRNA_ID_2778207 RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_126808,RMVar_hsa_circ_180531,RMVar_hsa_circ_90544,RMVar_hsa_circ_180532,RMVar_hsa_circ_180533,RMVar_hsa_circ_180534 79242 RMVar_ID_79242 Human_SNP_ID_613740744 m1A Human chr16 + 88717139 88717139 88717139 GAGCAGTGGGAACCAGATGATGGCGATGAGGAAGAGGATGATGAGGCCACCCATGCCGTACTTGA GAGCAGTGGGAACCAGATGATGGCGATGAGGATGAGGATGATGAGGCCACCCATGCCGTACTTGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88717090..88717156 26863196 MeRIP-seq:(Medium) rs889597047 Functional Loss SNV dbSNP153 33..33 33 - - - 79243 RMVar_ID_79243 Human_SNP_ID_613740770 m1A Human chr16 - 88717177 88717177 88717177 ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGAAGATCGTCAAGTACGGCATGGGTGGCCTCATCA ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGATGATCGTCAAGTACGGCATGGGTGGCCTCATCA T A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88717002..88717407 26863196 MeRIP-seq:(Medium) rs1311091527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2489511,Human_RBP_ID_24544554,Human_RBP_ID_24558694,Human_RBP_ID_25241022 Human_Splice_Rec_1749790,Human_Splice_Rec_1749808,Human_Splice_Rec_1749842,Human_Splice_Rec_1749868 RMVar_hsa_circ_93984,RMVar_hsa_circ_80974,RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_180531,RMVar_hsa_circ_90544,RMVar_hsa_circ_180533,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_128141,RMVar_hsa_circ_180535,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_180540 79244 RMVar_ID_79244 Human_SNP_ID_613740771 m1A Human chr16 - 88717177 88717177 88717177 ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGAAGATCGTCAAGTACGGCATGGGTGGCCTCATCA ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGAGGATCGTCAAGTACGGCATGGGTGGCCTCATCA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88717002..88717407 26863196 MeRIP-seq:(Medium) rs1311091527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2489511,Human_RBP_ID_24544554,Human_RBP_ID_24558694,Human_RBP_ID_25241022 Human_Splice_Rec_1749790,Human_Splice_Rec_1749808,Human_Splice_Rec_1749842,Human_Splice_Rec_1749868 RMVar_hsa_circ_93984,RMVar_hsa_circ_80974,RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_180531,RMVar_hsa_circ_90544,RMVar_hsa_circ_180533,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_128141,RMVar_hsa_circ_180535,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_180540 79245 RMVar_ID_79245 Human_SNP_ID_613742078 m1A Human chr16 + 88719631 88719631 88719631 ATGATGAAGATGTTGGCATAGATGTCCTCCACACACATCCAGCTGGACAGGGACAGCGTGGTGTC ATGATGAAGATGTTGGCATAGATGTCCTCCACCCACATCCAGCTGGACAGGGACAGCGTGGTGTC A C AC138028.4 Ensembl:ENSG00000260121 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88719551..88719884 32194978 MeRIP-seq:(Medium) rs761342639 Functional Loss SNV dbSNP153 33..33 33 - - - 79246 RMVar_ID_79246 Human_SNP_ID_613742642 m1A Human chr16 - 88720527 88720527 88720527 GCCCAGGCTGAGCGCCCCCTTCCGCAGGGCCCAGGGCACATATCGGCCGCTACGGCGCTTCTTCC GCCCAGGCTGAGCGCCCCCTTCCGCAGGGCCCGGGGCACATATCGGCCGCTACGGCGCTTCTTCC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:88720476..88720665 26863196 MeRIP-seq:(Medium) rs538041221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5356119,Human_RBP_ID_22652539,Human_RBP_ID_26329351 Human_Splice_Rec_1749782 Human_miRNA_ID_2149126 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539 79247 RMVar_ID_79247 Human_SNP_ID_613742720 m1A Human chr16 + 88720607 88720607 88720607 CCACCCCCACTCCCCAGCTGCCCCCGGCCGCCATCACTCACAGGGACAGGCAGAAGCCCTGCAGC CCACCCCCACTCCCCAGCTGCCCCCGGCCGCCGTCACTCACAGGGACAGGCAGAAGCCCTGCAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88720601..88720625 32194978 MeRIP-seq:(Medium) rs558173397 Functional Loss SNV dbSNP153 33..33 33 - - - 79248 RMVar_ID_79248 Human_SNP_ID_613742797 m1A Human chr16 - 88720698 88720698 88720698 AAGAAGAGGGGGAGGAAGAGAAAGAGGCCCCCACGGGGAGAGAGAAGAGGCCAAGCCGCTCTGGA AAGAAGAGGGGGAGGAAGAGAAAGAGGCCCCCGCGGGGAGAGAGAAGAGGCCAAGCCGCTCTGGA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88720647..88720777 26863196 MeRIP-seq:(Medium) rs1422902558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6033,Human_RBP_ID_892810,Human_RBP_ID_3949690,Human_RBP_ID_4389210,Human_RBP_ID_5142062,Human_RBP_ID_8812143,Human_RBP_ID_18190607,Human_RBP_ID_18987171,Human_RBP_ID_22946470,Human_RBP_ID_25247219,Human_RBP_ID_26329354,Human_RBP_ID_27811322 Human_Splice_Rec_1749780,Human_Splice_Rec_1749781 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539 79249 RMVar_ID_79249 Human_SNP_ID_613742820 m1A Human chr16 - 88720724 88720723 88720724 CCCTACAGAAGCTGAGGACAGGGAGGAAGAAGAGGGGGAGGAAGAGAAAGAGGCCCCCACGGGGA CCCTACAGAAGCTGAGGACAGGGAGGAAGAAG_GGGGGAGGAAGAGAAAGAGGCCCCCACGGGGA CT C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:88720676..88720750 26863196 MeRIP-seq:(Medium) rs1020092001 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_44413,Human_RBP_ID_892810,Human_RBP_ID_3948072,Human_RBP_ID_4389213,Human_RBP_ID_5572170,Human_RBP_ID_18190607,Human_RBP_ID_18987171,Human_RBP_ID_26329354,Human_RBP_ID_27811322 Human_Splice_Rec_1749780 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539 79250 RMVar_ID_79250 Human_SNP_ID_613742823 m1A Human chr16 - 88720724 88720724 88720724 CCCTACAGAAGCTGAGGACAGGGAGGAAGAAGAGGGGGAGGAAGAGAAAGAGGCCCCCACGGGGA CCCTACAGAAGCTGAGGACAGGGAGGAAGAAGGGGGGGAGGAAGAGAAAGAGGCCCCCACGGGGA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:88720676..88720750 26863196 MeRIP-seq:(Medium) rs1284434606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44413,Human_RBP_ID_892810,Human_RBP_ID_3948072,Human_RBP_ID_4389213,Human_RBP_ID_5572170,Human_RBP_ID_18190607,Human_RBP_ID_18987171,Human_RBP_ID_26329354,Human_RBP_ID_27811322 Human_Splice_Rec_1749780 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539 79251 RMVar_ID_79251 Human_SNP_ID_613743008 m1A Human chr16 + 88721138 88721138 88721138 TGCAGTAGCCCCACTCAGAAAACTGGGTAGGCAGGAGGTTGTGAGGCAGGGCGCTTATACCGATG TGCAGTAGCCCCACTCAGAAAACTGGGTAGGCCGGAGGTTGTGAGGCAGGGCGCTTATACCGATG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88721134..88721429 26863196 MeRIP-seq:(Medium) rs1300942926 Functional Loss SNV dbSNP153 33..33 33 - - - 79252 RMVar_ID_79252 Human_SNP_ID_613743173 m1A Human chr16 - 88721325 88721325 88721325 GAGCCGAGGAGGGGCCAGGGGTGCCTGCGGCCACCACCGAAGACCACATTCAGGTGGAAGCCAGG GAGCCGAGGAGGGGCCAGGGGTGCCTGCGGCCGCCACCGAAGACCACATTCAGGTGGAAGCCAGG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:88721276..88721375 26863196 MeRIP-seq:(Medium) rs1254574443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5524733,Human_RBP_ID_18987174,Human_RBP_ID_22441653,Human_RBP_ID_22583182,Human_RBP_ID_26329356 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_128015,RMVar_hsa_circ_180543 79253 RMVar_ID_79253 Human_SNP_ID_613743399 m1A Human chr16 - 88721650 88721650 88721650 CTGGAACAGCCACGTGGTGCTGCGGCGCTACGAGAACAAGCCCTACTTCCCGCCCCGCATCCTGG CTGGAACAGCCACGTGGTGCTGCGGCGCTACGCGAACAAGCCCTACTTCCCGCCCCGCATCCTGG T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88721599..88721667 26863196 MeRIP-seq:(Medium) rs530387460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_299221,Human_RBP_ID_9257084,Human_RBP_ID_22053562,Human_RBP_ID_22943395 Human_Splice_Rec_1749776 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_128015,RMVar_hsa_circ_100250,RMVar_hsa_circ_180543,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79254 RMVar_ID_79254 Human_SNP_ID_613743656 m1A Human chr16 + 88721948 88721948 88721948 CGTGACCATGTGGTTGAGGATGATGATGAAGTAGCAGAGCAGCTCCGAGTGGGCGGCCACACACT CGTGACCATGTGGTTGAGGATGATGATGAAGTGGCAGAGCAGCTCCGAGTGGGCGGCCACACACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88721899..88722006 26863196 MeRIP-seq:(Medium) rs995655988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8441879 79255 RMVar_ID_79255 Human_SNP_ID_613743728 m1A Human chr16 - 88722056 88722056 88722056 AAACACGCGGGTCTCCCTGTAGGCGCCTGCGCATCCCAGAGCTGGAGGAGGCAGAGCTGTTTGCG AAACACGCGGGTCTCCCTGTAGGCGCCTGCGCTTCCCAGAGCTGGAGGAGGCAGAGCTGTTTGCG T A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88721859..88722086 26863196 MeRIP-seq:(Medium) rs1269337246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5361176,Human_RBP_ID_17882541 Human_Splice_Rec_1749774 Human_miRNA_ID_2425192,Human_miRNA_ID_2434854 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_128015,RMVar_hsa_circ_100250,RMVar_hsa_circ_180543,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79256 RMVar_ID_79256 Human_SNP_ID_613743928 m1A Human chr16 - 88722301 88722301 88722301 GGCTACCACACGCGCAGTGGCAGTGAGGAGGCAGTCACCGACCCCGGGGAGCGTGAGGCTGGTGC GGCTACCACACGCGCAGTGGCAGTGAGGAGGCGGTCACCGACCCCGGGGAGCGTGAGGCTGGTGC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:88722251..88722325;chr16:88722251..88722400 26863196 MeRIP-seq:(Medium) rs35375982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1749772,Human_Splice_Rec_1749773 Human_miRNA_ID_2037785,Human_miRNA_ID_2348485 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79257 RMVar_ID_79257 Human_SNP_ID_613743990 m1A Human chr16 + 88722397 88722397 88722397 ATGCTGCTGAGTGGCTCCTCCGCGCCCAGCCCACTGGGGAGGGAAGCCGAGTCACAGAGAATCCT ATGCTGCTGAGTGGCTCCTCCGCGCCCAGCCCGCTGGGGAGGGAAGCCGAGTCACAGAGAATCCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:88722351..88722400 26863196 MeRIP-seq:(Medium) rs539832134 Functional Loss SNV dbSNP153 33..33 33 - - - 79258 RMVar_ID_79258 Human_SNP_ID_613744128 m1A Human chr16 - 88722593 88722593 88722593 CAGGCCCCACCGAGGCCCCCAATGCCCCAAGCACCGTGTCCAGGTAGGTGCGGGGGTGACCCGAG CAGGCCCCACCGAGGCCCCCAATGCCCCAAGCGCCGTGTCCAGGTAGGTGCGGGGGTGACCCGAG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:88722576..88722700 26863196 MeRIP-seq:(Medium) rs1346819182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19072350 Human_Splice_Rec_1749770,Human_Splice_Rec_1749771,Human_Splice_Rec_1749886 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79259 RMVar_ID_79259 Human_SNP_ID_613744162 m1A Human chr16 - 88722637 88722632 88722638 CGTGCTGGATCAGCTGTACACAAGCCAGGCCGAGGCCACGCTGCCAGGCCCCACCGAGGCCCCCA CGTGCTGGATCAGCTGTACACAAGCCAGGCC______ACGCTGCCAGGCCCCACCGAGGCCCCCA TGGCCTC T PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88722550..88722709 26863196 MeRIP-seq:(Medium) rs1339403716 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_44423,Human_RBP_ID_5524735,Human_RBP_ID_18190609,Human_RBP_ID_18469827,Human_RBP_ID_22532723 Human_Splice_Rec_1749770,Human_Splice_Rec_1749771,Human_Splice_Rec_1749886 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79260 RMVar_ID_79260 Human_SNP_ID_613744166 m1A Human chr16 - 88722637 88722637 88722637 CGTGCTGGATCAGCTGTACACAAGCCAGGCCGAGGCCACGCTGCCAGGCCCCACCGAGGCCCCCA CGTGCTGGATCAGCTGTACACAAGCCAGGCCGCGGCCACGCTGCCAGGCCCCACCGAGGCCCCCA T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88722550..88722709 26863196 MeRIP-seq:(Medium) rs1356282619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44423,Human_RBP_ID_5524735,Human_RBP_ID_18190609,Human_RBP_ID_18469827,Human_RBP_ID_22532723 Human_Splice_Rec_1749770,Human_Splice_Rec_1749771,Human_Splice_Rec_1749886 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79261 RMVar_ID_79261 Human_SNP_ID_613744346 m1A Human chr16 + 88722889 88722889 88722889 GGAGGTAGCGCTCTGCCCGCAGCACGTCGCTCATGGTGCCGTGGTGCCGGGTGAACTCCTGCAGC GGAGGTAGCGCTCTGCCCGCAGCACGTCGCTCGTGGTGCCGTGGTGCCGGGTGAACTCCTGCAGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88722876..88722900 26863196 MeRIP-seq:(Medium) rs1475985771 Functional Loss SNV dbSNP153 33..33 33 - - - 79262 RMVar_ID_79262 Human_SNP_ID_613744354 m1A Human chr16 - 88722898 88722898 88722898 GACACGCTGGCTGCAGGAGTTCACCCGGCACCACGGCACCATGAGCGACGTGCTGCGGGCAGAGC GACACGCTGGCTGCAGGAGTTCACCCGGCACCGCGGCACCATGAGCGACGTGCTGCGGGCAGAGC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:88722876..88722900 26863196 MeRIP-seq:(Medium) rs1243746484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6037 Human_Splice_Rec_1749769,Human_Splice_Rec_1749885 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79263 RMVar_ID_79263 Human_SNP_ID_613744385 m1A Human chr16 - 88722949 88722949 88722949 GAGCACGGCGCAGTTCCTGTGGATGCTGGGGCAGGCGCTAGTGGATGAGCTGACACGCTGGCTGC GAGCACGGCGCAGTTCCTGTGGATGCTGGGGCTGGCGCTAGTGGATGAGCTGACACGCTGGCTGC T A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88722902..88723325 26863196 MeRIP-seq:(Medium) rs767365106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3949700,Human_RBP_ID_5316939,Human_RBP_ID_9285982,Human_RBP_ID_18984432 Human_Splice_Rec_1749768,Human_Splice_Rec_1749884,Human_Splice_Rec_1749896 Human_miRNA_ID_2152002,Human_miRNA_ID_2420466 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79264 RMVar_ID_79264 Human_SNP_ID_613744386 m1A Human chr16 - 88722949 88722949 88722949 GAGCACGGCGCAGTTCCTGTGGATGCTGGGGCAGGCGCTAGTGGATGAGCTGACACGCTGGCTGC GAGCACGGCGCAGTTCCTGTGGATGCTGGGGCCGGCGCTAGTGGATGAGCTGACACGCTGGCTGC T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88722902..88723325 26863196 MeRIP-seq:(Medium) rs767365106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3949700,Human_RBP_ID_5316939,Human_RBP_ID_9285982,Human_RBP_ID_18984432 Human_Splice_Rec_1749768,Human_Splice_Rec_1749884,Human_Splice_Rec_1749896 Human_miRNA_ID_2152002,Human_miRNA_ID_2420466 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545 79265 RMVar_ID_79265 Human_SNP_ID_613744641 m1A Human chr16 - 88723252 88723252 88723252 GCGGCGGCAGCAGGAGCAGGAGCAGGCAAGGCAGGAACAGGCAGGACAGCTACCCACAGGTGAGC GCGGCGGCAGCAGGAGCAGGAGCAGGCAAGGCCGGAACAGGCAGGACAGCTACCCACAGGTGAGC T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88723064..88723356 26863196 MeRIP-seq:(Medium) rs1260569461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5572180,Human_RBP_ID_22474034 Human_Splice_Rec_1749764,Human_Splice_Rec_1749765,Human_Splice_Rec_1749880,Human_Splice_Rec_1749881,Human_Splice_Rec_1749892,Human_Splice_Rec_1749893 Human_miRNA_ID_1979453 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79266 RMVar_ID_79266 Human_SNP_ID_613744980 m1A Human chr16 - 88723882 88723882 88723882 CTGTTCCTGAAGACCCGAGGCCGTCGGCACAGAGTGCCTTCCAGGTGAGGTGGGAGAGCCCCGTC CTGTTCCTGAAGACCCGAGGCCGTCGGCACAGCGTGCCTTCCAGGTGAGGTGGGAGAGCCCCGTC T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88723876..88723900 26863196 MeRIP-seq:(Medium) rs758682817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233460,Human_RBP_ID_892815,Human_RBP_ID_5572181,Human_RBP_ID_18469830,Human_RBP_ID_18984434,Human_RBP_ID_26328257 Human_Splice_Rec_1749762,Human_Splice_Rec_1749763,Human_Splice_Rec_1749879,Human_Splice_Rec_1749890,Human_Splice_Rec_1749891,Human_Splice_Rec_1749900 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_41249,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79267 RMVar_ID_79267 Human_SNP_ID_613745007 m1A Human chr16 - 88723917 88723914 88723917 CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGAGGCTGTTCCTGAAGACCCGAGGCCGTCGGCAC CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGG___CTGTTCCTGAAGACCCGAGGCCGTCGGCAC GCCT G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88723794..88723975 26863196 MeRIP-seq:(Medium) rs1473113482 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_233460,Human_RBP_ID_892815,Human_RBP_ID_3948079,Human_RBP_ID_18469830,Human_RBP_ID_18984434,Human_RBP_ID_26328257 Human_Splice_Rec_1749762,Human_Splice_Rec_1749763,Human_Splice_Rec_1749879,Human_Splice_Rec_1749890,Human_Splice_Rec_1749891,Human_Splice_Rec_1749900 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_41249,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79268 RMVar_ID_79268 Human_SNP_ID_613745012 m1A Human chr16 - 88723917 88723917 88723917 CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGAGGCTGTTCCTGAAGACCCGAGGCCGTCGGCAC CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGTGGCTGTTCCTGAAGACCCGAGGCCGTCGGCAC T A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88723794..88723975 26863196 MeRIP-seq:(Medium) rs202066744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233460,Human_RBP_ID_892815,Human_RBP_ID_3948079,Human_RBP_ID_18469830,Human_RBP_ID_18984434,Human_RBP_ID_26328257 Human_Splice_Rec_1749762,Human_Splice_Rec_1749763,Human_Splice_Rec_1749879,Human_Splice_Rec_1749890,Human_Splice_Rec_1749891,Human_Splice_Rec_1749900 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_41249,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79269 RMVar_ID_79269 Human_SNP_ID_613745013 m1A Human chr16 - 88723917 88723917 88723917 CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGAGGCTGTTCCTGAAGACCCGAGGCCGTCGGCAC CCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGCGGCTGTTCCTGAAGACCCGAGGCCGTCGGCAC T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88723794..88723975 26863196 MeRIP-seq:(Medium) rs202066744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233460,Human_RBP_ID_892815,Human_RBP_ID_3948079,Human_RBP_ID_18469830,Human_RBP_ID_18984434,Human_RBP_ID_26328257 Human_Splice_Rec_1749762,Human_Splice_Rec_1749763,Human_Splice_Rec_1749879,Human_Splice_Rec_1749890,Human_Splice_Rec_1749891,Human_Splice_Rec_1749900 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_41249,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79270 RMVar_ID_79270 Human_SNP_ID_613745016 m1A Human chr16 - 88723920 88723920 88723920 CTTCCTGTTTGAGTCCGACAGTGAGGAAGAGGAGGAGGCTGTTCCTGAAGACCCGAGGCCGTCGG CTTCCTGTTTGAGTCCGACAGTGAGGAAGAGGGGGAGGCTGTTCCTGAAGACCCGAGGCCGTCGG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88723836..88723989;chr16:88723851..88723975 26863196 MeRIP-seq:(Medium) rs918454892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233460,Human_RBP_ID_892815,Human_RBP_ID_3948079,Human_RBP_ID_4389252,Human_RBP_ID_18984434,Human_RBP_ID_26328257 Human_Splice_Rec_1749762,Human_Splice_Rec_1749763,Human_Splice_Rec_1749879,Human_Splice_Rec_1749890,Human_Splice_Rec_1749891,Human_Splice_Rec_1749900 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_95765,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_100250,RMVar_hsa_circ_41249,RMVar_hsa_circ_116774,RMVar_hsa_circ_180544,RMVar_hsa_circ_180545,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_53140 79271 RMVar_ID_79271 Human_SNP_ID_613746005 m1A Human chr16 + 88725617 88725617 88725617 AGGCACCTACTGTCTTTTCAGCTGGGCCAGGGACTTCTCCTCTATCCTGCGGTGAAAGTCAATGC AGGCACCTACTGTCTTTTCAGCTGGGCCAGGGCCTTCTCCTCTATCCTGCGGTGAAAGTCAATGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88725384..88725701 26863196 MeRIP-seq:(Medium) rs373732822 Functional Loss SNV dbSNP153 33..33 33 - - - 79272 RMVar_ID_79272 Human_SNP_ID_613746451 m1A Human chr16 + 88726347 88726347 88726347 CGGCCCTGACGTGCAGGTAGTAATGGCTAAGGAAGACGCGGCGCTGCAGCAGCAGGAAGAAGAAG CGGCCCTGACGTGCAGGTAGTAATGGCTAAGGGAGACGCGGCGCTGCAGCAGCAGGAAGAAGAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88726278..88726489 26863196 MeRIP-seq:(Medium) rs1161441775 Functional Loss SNV dbSNP153 33..33 33 - - - 79273 RMVar_ID_79273 Human_SNP_ID_613746476 m1A Human chr16 + 88726393 88726393 88726393 CAGCAGCAGGAAGAAGAAGCAGACGCTGTCCCAGATGATGCCAGCCTCCTCCACAGGCAGCAGGC CAGCAGCAGGAAGAAGAAGCAGACGCTGTCCCCGATGATGCCAGCCTCCTCCACAGGCAGCAGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88726276..88726425 26863196 MeRIP-seq:(Medium) rs749496092 Functional Loss SNV dbSNP153 33..33 33 - - - 79274 RMVar_ID_79274 Human_SNP_ID_613746488 m1A Human chr16 + 88726426 88726406 88726427 GATGATGCCAGCCTCCTCCACAGGCAGCAGGCAGTCCTGGTCTCTGTCCATCATCTCCTTGGCTG GATGATGCCAGCC_____________________TCCTGGTCTCTGTCCATCATCTCCTTGGCTG CTCCTCCACAGGCAGCAGGCAG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88726376..88726475 32194978 MeRIP-seq:(Medium) rs1567665891 Functional Loss DEL dbSNP153 14..34 33 - - - 79275 RMVar_ID_79275 Human_SNP_ID_613746499 m1A Human chr16 + 88726426 88726426 88726426 GATGATGCCAGCCTCCTCCACAGGCAGCAGGCAGTCCTGGTCTCTGTCCATCATCTCCTTGGCTG GATGATGCCAGCCTCCTCCACAGGCAGCAGGCCGTCCTGGTCTCTGTCCATCATCTCCTTGGCTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88726376..88726475 32194978 MeRIP-seq:(Medium) rs962490141 Functional Loss SNV dbSNP153 33..33 33 - - - 79276 RMVar_ID_79276 Human_SNP_ID_613746832 m1A Human chr16 - 88726800 88726800 88726800 CTACCTGCTGCTCTTCGGCACGGCCCTGCTGCAGAGGGACACACGGGCCCGCCTCGTGCTGTGGG CTACCTGCTGCTCTTCGGCACGGCCCTGCTGCGGAGGGACACACGGGCCCGCCTCGTGCTGTGGG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr16:88726751..88726800 26863196,32194978 MeRIP-seq:(Medium) rs1203783140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22532860 Human_Splice_Rec_1749753 Human_miRNA_ID_2956300 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_315316 79277 RMVar_ID_79277 Human_SNP_ID_613747117 m1A Human chr16 - 88727194 88727194 88727194 CGTGTGGCACAGCGGCGGCTCCTGTGTCCTGCAGGCGACTTTCTCCTGCTGCTGTGCGCCTCCCA CGTGTGGCACAGCGGCGGCTCCTGTGTCCTGCGGGCGACTTTCTCCTGCTGCTGTGCGCCTCCCA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88727026..88727206 26863196 MeRIP-seq:(Medium) rs774265673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17256859 RMVar_hsa_circ_13689,RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_315316 79278 RMVar_ID_79278 Human_SNP_ID_613749367 m1A Human chr16 - 88731933 88731933 88731933 AGTCCCTCCCCCCAGACTCAGTGCATCCCCACACCCCGCCCTCTCCCCTCCCCAGATCTGCTTCC AGTCCCTCCCCCCAGACTCAGTGCATCCCCACGCCCCGCCCTCTCCCCTCCCCAGATCTGCTTCC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88731672..88731957 26863196 MeRIP-seq:(Medium) rs76070043 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5128270,Human_RBP_ID_17077723,Human_RBP_ID_18939690,Human_RBP_ID_26779829,Human_RBP_ID_27837952 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548 79279 RMVar_ID_79279 Human_SNP_ID_613749721 m1A Human chr16 + 88732345 88732345 88732345 GGAGGCAATGTCCTTGCCTCACCTCCAGCCCGAATTTGTAGAAGAAGAAGTTGATGAAGTACTTG GGAGGCAATGTCCTTGCCTCACCTCCAGCCCGCATTTGTAGAAGAAGAAGTTGATGAAGTACTTG A C AC138028.2 Ensembl:ENSG00000224888 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88732327..88732480 26863196 MeRIP-seq:(Medium) rs1249405005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12844657 79280 RMVar_ID_79280 Human_SNP_ID_613749817 m1A Human chr16 - 88732480 88732480 88732480 GCTGGTATTCGAGGCCATCGTGTACCGGCGCCAGGAGCACTACCGCCGGCAGCACCAGCTGGCCC GCTGGTATTCGAGGCCATCGTGTACCGGCGCCGGGAGCACTACCGCCGGCAGCACCAGCTGGCCC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88732433..88732754 32194978 MeRIP-seq:(Medium) rs1334447483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18469835,Human_RBP_ID_27812044 Human_Splice_Rec_1749744,Human_Splice_Rec_1749904 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_94825,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_180549 79281 RMVar_ID_79281 Human_SNP_ID_613750364 m1A Human chr16 - 88733402 88733402 88733402 GCTGGTGGTGCTGTGGGCCTTCGCCCTGCCCTACCCACGCTTCCGGCCCATGGCCTCCTGCCTGT GCTGGTGGTGCTGTGGGCCTTCGCCCTGCCCTCCCCACGCTTCCGGCCCATGGCCTCCTGCCTGT T G PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:88733351..88733450 26863196 MeRIP-seq:(Medium) rs1054133228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233462,Human_RBP_ID_3948103,Human_RBP_ID_9285988,Human_RBP_ID_17690998,Human_RBP_ID_18469934,Human_RBP_ID_18987191,Human_RBP_ID_22207160 Human_Splice_Rec_1749740 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_94825,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_180549 79282 RMVar_ID_79282 Human_SNP_ID_613752036 m1A Human chr16 - 88736233 88736233 88736233 ACGCTACGTGTGGGCCATGGACCTGCGCCCTGAGCTGCCCACCACCCTGGGCCCCGTCAGCCTGC ACGCTACGTGTGGGCCATGGACCTGCGCCCTGGGCTGCCCACCACCCTGGGCCCCGTCAGCCTGC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88736183..88736422 26863196 MeRIP-seq:(Medium) rs1382907778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44466,Human_RBP_ID_233465,Human_RBP_ID_894423 Human_Splice_Rec_1749727 Human_miRNA_ID_2354148 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_109147,RMVar_hsa_circ_94825,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_115006,RMVar_hsa_circ_180549,RMVar_hsa_circ_180550,RMVar_hsa_circ_75665,RMVar_hsa_circ_180552,RMVar_hsa_circ_180553,RMVar_hsa_circ_98554,RMVar_hsa_circ_180555 79283 RMVar_ID_79283 Human_SNP_ID_613752045 m1A Human chr16 - 88736249 88736249 88736249 TGACGCTGTGCTGCCTACGCTACGTGTGGGCCATGGACCTGCGCCCTGAGCTGCCCACCACCCTG TGACGCTGTGCTGCCTACGCTACGTGTGGGCCGTGGACCTGCGCCCTGAGCTGCCCACCACCCTG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88736201..88738651 32194978 MeRIP-seq:(Medium) rs986221836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1524713 Human_miRNA_ID_2354148 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_109147,RMVar_hsa_circ_94825,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_115006,RMVar_hsa_circ_180549,RMVar_hsa_circ_180550,RMVar_hsa_circ_75665,RMVar_hsa_circ_180552,RMVar_hsa_circ_180553,RMVar_hsa_circ_98554,RMVar_hsa_circ_180555 79284 RMVar_ID_79284 Human_SNP_ID_613752642 m1A Human chr16 - 88737288 88737288 88737288 CGTTGATCCCCAAGACCCCATGGGGGGCCTCCAGGTCCCCCAACCCCTCCCCAGAGAATGTGGCT CGTTGATCCCCAAGACCCCATGGGGGGCCTCCGGGTCCCCCAACCCCTCCCCAGAGAATGTGGCT T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88737279..88737380 26863196 MeRIP-seq:(Medium) rs1199611828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5142063,Human_RBP_ID_17078346,Human_RBP_ID_21973300,Human_RBP_ID_27838308 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_126889,RMVar_hsa_circ_180547,RMVar_hsa_circ_109147,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_115006,RMVar_hsa_circ_180550,RMVar_hsa_circ_75665,RMVar_hsa_circ_180552,RMVar_hsa_circ_180553,RMVar_hsa_circ_98554,RMVar_hsa_circ_180555 79285 RMVar_ID_79285 Human_SNP_ID_613752915 m1A Human chr16 - 88737648 88737648 88737648 AGCCCGTGCATGGCTCAGCGCTGCTTGCCCACAGCACGTGGTGCCCACAGCACCCGACACCGAGG AGCCCGTGCATGGCTCAGCGCTGCTTGCCCACGGCACGTGGTGCCCACAGCACCCGACACCGAGG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88737597..88737681 26863196 MeRIP-seq:(Medium) rs1442173708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18686763 Human_Splice_Rec_1749723 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_109147,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_115006,RMVar_hsa_circ_180550,RMVar_hsa_circ_75665,RMVar_hsa_circ_180552,RMVar_hsa_circ_180553 79286 RMVar_ID_79286 Human_SNP_ID_613753025 m1A Human chr16 - 88737807 88737807 88737811 GGGCTCAAGACGCTGGTCTCTGCAGAGGAAGGAGGCGGCAAAGGGGTATGAGGCTCGGGAGCTGG GGGCTCAAGACGCTGGTCTCTGCAGAGGGAGGCGGCGGCAAAGGGGTATGAGGCTCGGGAGCTGG TCCTT GCCTC PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88737776..88737825 26863196 MeRIP-seq:(Medium) rs1555556846 Functional Loss MNV dbSNP153 29..33 33 - - - Human_RBP_ID_22532731 Human_Splice_Rec_1749720,Human_Splice_Rec_1749721 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_180538,RMVar_hsa_circ_67228,RMVar_hsa_circ_109147,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548,RMVar_hsa_circ_115006,RMVar_hsa_circ_180550,RMVar_hsa_circ_75665,RMVar_hsa_circ_180552,RMVar_hsa_circ_180553 79287 RMVar_ID_79287 Human_SNP_ID_613759005 m1A Human chr16 - 88750487 88750487 88750487 CGGGACCTTCTGGGACAGGCAGGAGGGCAGACACGGGACATGGTGTGGGGGCTGTGGCGAGTGCG CGGGACCTTCTGGGACAGGCAGGAGGGCAGACCCGGGACATGGTGTGGGGGCTGTGGCGAGTGCG T G PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88750444..88750601 26863196 MeRIP-seq:(Medium) rs1397884966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503324,Human_RBP_ID_8085808,Human_RBP_ID_8185343,Human_RBP_ID_22713448 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79288 RMVar_ID_79288 Human_SNP_ID_613762106 m1A Human chr16 - 88758320 88758320 88758320 CTGGGATGCAGCACGATGTTGGTCTGTCAGGGAGTGGCAGGAAGCCCACAGGGTCAGCTGACACT CTGGGATGCAGCACGATGTTGGTCTGTCAGGGCGTGGCAGGAAGCCCACAGGGTCAGCTGACACT T G PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88758318..88758516 26863196 MeRIP-seq:(Medium) rs529371275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503333,Human_RBP_ID_8185374,Human_RBP_ID_9420149,Human_RBP_ID_12844832,Human_RBP_ID_18485428,Human_RBP_ID_20160632,Human_RBP_ID_22713460 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79289 RMVar_ID_79289 Human_SNP_ID_613762118 m1A Human chr16 - 88758355 88758355 88758355 GTTGCCCCCAGGCCAGGCCACTGCTGGGGCCAAGGCTGGGATGCAGCACGATGTTGGTCTGTCAG GTTGCCCCCAGGCCAGGCCACTGCTGGGGCCAGGGCTGGGATGCAGCACGATGTTGGTCTGTCAG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88758324..88758490 26863196 MeRIP-seq:(Medium) rs1191516176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5647268,Human_RBP_ID_8185375,Human_RBP_ID_9420149,Human_RBP_ID_22498564 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79290 RMVar_ID_79290 Human_SNP_ID_613762661 m1A Human chr16 + 88759944 88759944 88759944 TCCCCCAATGGAGGCCGAGCCCGGCCAGGCCCACCTTCACCAGCCACCCTGGCATCCGGGCCTGC TCCCCCAATGGAGGCCGAGCCCGGCCAGGCCCGCCTTCACCAGCCACCCTGGCATCCGGGCCTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88759941..88760228 26863196 MeRIP-seq:(Medium) rs1172179086 Functional Loss SNV dbSNP153 33..33 33 - - - 79291 RMVar_ID_79291 Human_SNP_ID_613766824 m1A Human chr16 - 88771656 88771656 88771656 CTCTGCAACCTTGTCCCACCCAGCACCTCCCTATGGCCCTGCTCTGACTGTGGGCTGAGGGGGAC CTCTGCAACCTTGTCCCACCCAGCACCTCCCTTTGGCCCTGCTCTGACTGTGGGCTGAGGGGGAC T A PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88771649..88771741 26863196 MeRIP-seq:(Medium) rs902475118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_198857,Human_RBP_ID_2489626,Human_RBP_ID_3503349,Human_RBP_ID_8185425,Human_RBP_ID_9326286 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79292 RMVar_ID_79292 Human_SNP_ID_613766842 m1A Human chr16 + 88771715 88771715 88771715 GCAGAGGTGACACTAGTGGAGCCGACGTCCAGATGCCCGTCCACCCGCGGCCCCAGGCCCTCCTG GCAGAGGTGACACTAGTGGAGCCGACGTCCAGTTGCCCGTCCACCCGCGGCCCCAGGCCCTCCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88771516..88771752 26863196 MeRIP-seq:(Medium) rs1322383354 Functional Loss SNV dbSNP153 33..33 33 - - - 79293 RMVar_ID_79293 Human_SNP_ID_613766906 m1A Human chr16 + 88771943 88771943 88771943 CTCTATGCCCGTCCACCCGCGGCCCCAGGCCCACCTGAGACTCTATGCCCGTCCACCCGCGGCCC CTCTATGCCCGTCCACCCGCGGCCCCAGGCCCGCCTGAGACTCTATGCCCGTCCACCCGCGGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88771901..88772000 26863196 MeRIP-seq:(Medium) rs113126532 Functional Loss SNV dbSNP153 33..33 33 - - - 79294 RMVar_ID_79294 Human_SNP_ID_613766907 m1A Human chr16 + 88771943 88771943 88771943 CTCTATGCCCGTCCACCCGCGGCCCCAGGCCCACCTGAGACTCTATGCCCGTCCACCCGCGGCCC CTCTATGCCCGTCCACCCGCGGCCCCAGGCCCTCCTGAGACTCTATGCCCGTCCACCCGCGGCCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88771901..88772000 26863196 MeRIP-seq:(Medium) rs113126532 Functional Loss SNV dbSNP153 33..33 33 - - - 79295 RMVar_ID_79295 Human_SNP_ID_613766920 m1A Human chr16 - 88772080 88772001 88772081 AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGACAGGCATAGAGTCTCAGGTGGGCCTGGGGCCGCG AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGA__________________________________ ATCCACCCGCGGCCCCAGGCCCTCCTGAGACTCTATGCCCGTCCACCCGCGGCCCCAGGCCCACCTGAGACTCTATGCCTG A PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88772026..88772150 26863196 MeRIP-seq:(Medium) rs1567694749 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_8185429,Human_RBP_ID_18686818 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79296 RMVar_ID_79296 Human_SNP_ID_613766937 m1A Human chr16 - 88772080 88772040 88772080 AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGACAGGCATAGAGTCTCAGGTGGGCCTGGGGCCGCG AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGAC_________________________________ CGTCCACCCGCGGCCCCAGGCCCACCTGAGACTCTATGCCT C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88772026..88772150 26863196 MeRIP-seq:(Medium) rs1233590041 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_8185429,Human_RBP_ID_18686818 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79297 RMVar_ID_79297 Human_SNP_ID_613766954 m1A Human chr16 - 88772080 88772080 88772080 AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGACAGGCATAGAGTCTCAGGTGGGCCTGGGGCCGCG AGTCTCAGGAGGGCCTGGGGCCGCGGGTGGACGGGCATAGAGTCTCAGGTGGGCCTGGGGCCGCG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88772026..88772150 26863196 MeRIP-seq:(Medium) rs1252719959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8185429,Human_RBP_ID_18686818 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 79298 RMVar_ID_79298 Human_SNP_ID_613771661 m1A Human chr16 - 88785164 88785164 88785164 GGCCCCAGTGAGCCGAGCGCTGCGCTCCGCCGAGGGGCAGGGCGGTCGCCTGAGCGAGCGCGGGC GGCCCCAGTGAGCCGAGCGCTGCGCTCCGCCGGGGGGCAGGGCGGTCGCCTGAGCGAGCGCGGGC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88785007..88785225 26863196 MeRIP-seq:(Medium) rs879375075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4389457,Human_RBP_ID_8726421,Human_RBP_ID_9326291,Human_RBP_ID_18419497,Human_RBP_ID_18469843,Human_RBP_ID_22532867 79299 RMVar_ID_79299 Human_SNP_ID_613771662 m1A Human chr16 - 88785164 88785164 88785164 GGCCCCAGTGAGCCGAGCGCTGCGCTCCGCCGAGGGGCAGGGCGGTCGCCTGAGCGAGCGCGGGC GGCCCCAGTGAGCCGAGCGCTGCGCTCCGCCGCGGGGCAGGGCGGTCGCCTGAGCGAGCGCGGGC T G PIEZO1 Ensembl:ENSG00000103335 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88785007..88785225 26863196 MeRIP-seq:(Medium) rs879375075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4389457,Human_RBP_ID_8726421,Human_RBP_ID_9326291,Human_RBP_ID_18419497,Human_RBP_ID_18469843,Human_RBP_ID_22532867 79300 RMVar_ID_79300 Human_SNP_ID_613776215 m1A Human chr16 + 88798241 88798241 88798241 TGATGGTGATGGTGAGGATGGTGATGATGATGATGGTGGTGATGGTGAGGATGGTGGTGATGATG TGATGGTGATGGTGAGGATGGTGATGATGATGGTGGTGGTGATGGTGAGGATGGTGGTGATGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88798239..88798444 26863196 MeRIP-seq:(Medium) rs922181879 Functional Loss SNV dbSNP153 33..33 33 - - - 79301 RMVar_ID_79301 Human_SNP_ID_613778577 m1A Human chr16 + 88803854 88803854 88803854 CTCCGCCGCCATGGAGCAGCGCCGCGTCACCGACTTCTTCGCGCGCCGCCGCCCCGGGCCCCCCC CTCCGCCGCCATGGAGCAGCGCCGCGTCACCGCCTTCTTCGCGCGCCGCCGCCCCGGGCCCCCCC A C CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr16:88803801..88804075;chr16:88803803..88804074;chr16:88803776..88804050 26863196 MeRIP-seq:(Medium) rs1460180527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481583,Human_RBP_ID_1066488,Human_RBP_ID_1524815,Human_RBP_ID_4389466,Human_RBP_ID_17371566,Human_RBP_ID_22532733,Human_RBP_ID_27447122 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867 79302 RMVar_ID_79302 Human_SNP_ID_613778602 m1A Human chr16 - 88803905 88803905 88803905 CGGGCCTGGCGGGGCTGGGGGTGCGGCAGGCCAGCTTGGGCGGCGCGATGCGGGGGGGCCCGGGG CGGGCCTGGCGGGGCTGGGGGTGCGGCAGGCCGGCTTGGGCGGCGCGATGCGGGGGGGCCCGGGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:88803801..88804050 26863196 MeRIP-seq:(Medium) rs1048076521 Functional Loss SNV dbSNP153 33..33 33 - - - 79303 RMVar_ID_79303 Human_SNP_ID_613778605 m1A Human chr16 + 88803922 88803913 88803922 TCGCGCCGCCCAAGCTGGCCTGCCGCACCCCCAGCCCCGCCAGGCCCGCACTCCGCGCCCCGGCC TCGCGCCGCCCAAGCTGGCCTGCC_________GCCCCGCCAGGCCCGCACTCCGCGCCCCGGCC CGCACCCCCA C CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:88803801..88804075 26863196 MeRIP-seq:(Medium) rs939747416 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_233997,Human_RBP_ID_481586,Human_RBP_ID_1066488,Human_RBP_ID_4394089,Human_RBP_ID_5361223,Human_RBP_ID_17371567,Human_RBP_ID_22532733 Human_miRNA_ID_1357376,Human_miRNA_ID_2147108,Human_miRNA_ID_2685603,Human_miRNA_ID_2988533,Human_miRNA_ID_3022234,Human_miRNA_ID_3066190 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867 79304 RMVar_ID_79304 Human_SNP_ID_613778851 m1A Human chr16 + 88804498 88804498 88804498 TCTGATCCTTCGGGGTCCTCTGCAGAGCCAGGAGCACCAGGTCTTGTCATGAGTTCACCCTTGGG TCTGATCCTTCGGGGTCCTCTGCAGAGCCAGGGGCACCAGGTCTTGTCATGAGTTCACCCTTGGG A G CDT1 Ensembl:ENSG00000167513 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88804497..88804875 26863196 MeRIP-seq:(Medium) rs746723249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180557,RMVar_hsa_circ_116867 79305 RMVar_ID_79305 Human_SNP_ID_613778878 m1A Human chr16 - 88804527 88804527 88804527 ACTGGGGCTGGAAACCTGGTGGGAGGGACCCCAAGGGTGAACTCATGACAAGACCTGGTGCTCCT ACTGGGGCTGGAAACCTGGTGGGAGGGACCCCGAGGGTGAACTCATGACAAGACCTGGTGCTCCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:88804526..88804650;chr16:88804526..88804625;chr16:88804526..88804600 26863196 MeRIP-seq:(Medium) rs755120855 Functional Loss SNV dbSNP153 33..33 33 - - - 79306 RMVar_ID_79306 Human_SNP_ID_613778879 m1A Human chr16 - 88804527 88804527 88804527 ACTGGGGCTGGAAACCTGGTGGGAGGGACCCCAAGGGTGAACTCATGACAAGACCTGGTGCTCCT ACTGGGGCTGGAAACCTGGTGGGAGGGACCCCCAGGGTGAACTCATGACAAGACCTGGTGCTCCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr16:88804526..88804650;chr16:88804526..88804625;chr16:88804526..88804600 26863196 MeRIP-seq:(Medium) rs755120855 Functional Loss SNV dbSNP153 33..33 33 - - - 79307 RMVar_ID_79307 Human_SNP_ID_613778939 m1A Human chr16 + 88804614 88804602 88804615 CAGCCTGCCCTTCTCCGGGCCAGAAGATAAAGAAATCCACCCCGGCAGCAGGTCAGCCGCCCCAC CAGCCTGCCCTTCTCCGGGCC_____________ATCCACCCCGGCAGCAGGTCAGCCGCCCCAC CAGAAGATAAAGAA C CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88804505..88804758 26863196 MeRIP-seq:(Medium) rs1188624254 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_1366819,Human_RBP_ID_5128892,Human_RBP_ID_18686834 Human_Splice_Rec_1749920,Human_Splice_Rec_1749921,Human_Splice_Rec_1749937 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867,RMVar_hsa_circ_103617,RMVar_hsa_circ_180558 79308 RMVar_ID_79308 Human_SNP_ID_613779417 m1A Human chr16 - 88805513 88805513 88805513 GCGGAACATCTCCGCCAGCACCTGGTACTTGTAGGGCAGCACGAGTCCCGGCAGGCCGGGCTGGG GCGGAACATCTCCGCCAGCACCTGGTACTTGTGGGGCAGCACGAGTCCCGGCAGGCCGGGCTGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88803851..88808511 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 79309 RMVar_ID_79309 Human_SNP_ID_613780859 m1A Human chr16 + 88808255 88808254 88808256 TCGCCCACATCACTGCACGCCTGGCCCACCAGACACGTGCTGAGGAGGGGCTGTGAGCCTGGGGG TCGCCCACATCACTGCACGCCTGGCCCACCAG__ACGTGCTGAGGAGGGGCTGTGAGCCTGGGGG GAC G CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88808205..88808326 26863196 MeRIP-seq:(Medium) rs1396222116 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_481597,Human_RBP_ID_1524849,Human_RBP_ID_4389539,Human_RBP_ID_6545618,Human_RBP_ID_17882609,Human_RBP_ID_22945163,Human_RBP_ID_23128724,Human_RBP_ID_27248173,Human_RBP_ID_27447131 Human_miRNA_ID_2141464 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867,RMVar_hsa_circ_86282,RMVar_hsa_circ_103617,RMVar_hsa_circ_180558,RMVar_hsa_circ_94978,RMVar_hsa_circ_111850,RMVar_hsa_circ_180559,RMVar_hsa_circ_180560,RMVar_hsa_circ_104261,RMVar_hsa_circ_180561,RMVar_hsa_circ_115550,RMVar_hsa_circ_180562,RMVar_hsa_circ_180563 79310 RMVar_ID_79310 Human_SNP_ID_613780862 m1A Human chr16 + 88808255 88808255 88808255 TCGCCCACATCACTGCACGCCTGGCCCACCAGACACGTGCTGAGGAGGGGCTGTGAGCCTGGGGG TCGCCCACATCACTGCACGCCTGGCCCACCAGGCACGTGCTGAGGAGGGGCTGTGAGCCTGGGGG A G CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88808205..88808326 26863196 MeRIP-seq:(Medium) rs1378352387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481597,Human_RBP_ID_1524849,Human_RBP_ID_4389539,Human_RBP_ID_6545618,Human_RBP_ID_17882609,Human_RBP_ID_22945163,Human_RBP_ID_23128724,Human_RBP_ID_27248173,Human_RBP_ID_27447131 Human_miRNA_ID_2141464 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867,RMVar_hsa_circ_86282,RMVar_hsa_circ_103617,RMVar_hsa_circ_180558,RMVar_hsa_circ_94978,RMVar_hsa_circ_111850,RMVar_hsa_circ_180559,RMVar_hsa_circ_180560,RMVar_hsa_circ_104261,RMVar_hsa_circ_180561,RMVar_hsa_circ_115550,RMVar_hsa_circ_180562,RMVar_hsa_circ_180563 79311 RMVar_ID_79311 Human_SNP_ID_613781503 m1A Human chr16 + 88809561 88809561 88809561 AACACAGCTTTGCCCCAGGCTTTGGCACTTCCAGCCCCAGGAGAGGCGCTGAACCCCAGCAAAGG AACACAGCTTTGCCCCAGGCTTTGGCACTTCCGGCCCCAGGAGAGGCGCTGAACCCCAGCAAAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88809501..88809826 32194978 MeRIP-seq:(Medium) rs895364227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1524885 79312 RMVar_ID_79312 Human_SNP_ID_613781794 m1A Human chr16 - 88810108 88810108 88810108 GGAGATTCAGAAAGACGCCCTGGAGCCAGGACAGAGGGTGGTCGTCGTGGATGATCTGCTGGCCA GGAGATTCAGAAAGACGCCCTGGAGCCAGGACGGAGGGTGGTCGTCGTGGATGATCTGCTGGCCA T C APRT Ensembl:ENSG00000198931 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs8191494 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_481632,Human_RBP_ID_892843,Human_RBP_ID_1524896,Human_RBP_ID_5114023,Human_RBP_ID_5142356,Human_RBP_ID_6545631,Human_RBP_ID_8442022,Human_RBP_ID_9326293,Human_RBP_ID_12845307,Human_RBP_ID_17653626,Human_RBP_ID_18190253,Human_RBP_ID_22441182,Human_RBP_ID_22944899 Human_Splice_Rec_1749956,Human_Splice_Rec_1749957,Human_Splice_Rec_1749963,Human_Splice_Rec_1749968,Human_Splice_Rec_1749969,Human_Splice_Rec_1749973,Human_Splice_Rec_1749977,Human_Splice_Rec_1749981,Human_Splice_Rec_1749986,Human_Splice_Rec_1749987,Human_Splice_Rec_1749989,Human_Splice_Rec_1749991 RMVar_hsa_circ_88457,RMVar_hsa_circ_117544,RMVar_hsa_circ_98626,RMVar_hsa_circ_180565,RMVar_hsa_circ_180567,RMVar_hsa_circ_80891,RMVar_hsa_circ_180568,RMVar_hsa_circ_180566 79313 RMVar_ID_79313 Human_SNP_ID_613782422 m1A Human chr16 - 88811556 88811556 88811556 TGAAGGCGACCCACGGGGGCCGCATCGACTACATCGCAGGCGAGTGCCCAGTGGCCGCATCTAGG TGAAGGCGACCCACGGGGGCCGCATCGACTACGTCGCAGGCGAGTGCCCAGTGGCCGCATCTAGG T C APRT Ensembl:ENSG00000198931 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:88811551..88811925 26863196 MeRIP-seq:(Medium) rs748942141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234315,Human_RBP_ID_817178,Human_RBP_ID_4394090,Human_RBP_ID_8442028,Human_RBP_ID_9326295,Human_RBP_ID_17882629,Human_RBP_ID_18190255,Human_RBP_ID_19072375,Human_RBP_ID_26810737,Human_RBP_ID_26951876,Human_RBP_ID_27248206 RMVar_hsa_circ_117544,RMVar_hsa_circ_180567,RMVar_hsa_circ_80891,RMVar_hsa_circ_180568 79314 RMVar_ID_79314 Human_SNP_ID_613782461 m1A Human chr16 + 88811609 88811606 88811609 GGGTCGCCTTCAGGTGTCGCGCCAGGAGGCCGATGGCGGCGCGGAAGGAGGCGGGGTCCTTCAGG GGGTCGCCTTCAGGTGTCGCGCCAGGAGGC___TGGCGGCGCGGAAGGAGGCGGGGTCCTTCAGG CCGA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:88811551..88811700 32194978 MeRIP-seq:(Medium) rs1567505671 Functional Loss DEL dbSNP153 31..33 33 - - - 79315 RMVar_ID_79315 Human_SNP_ID_613782462 m1A Human chr16 + 88811609 88811609 88811609 GGGTCGCCTTCAGGTGTCGCGCCAGGAGGCCGATGGCGGCGCGGAAGGAGGCGGGGTCCTTCAGG GGGTCGCCTTCAGGTGTCGCGCCAGGAGGCCGGTGGCGGCGCGGAAGGAGGCGGGGTCCTTCAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:88811551..88811700 32194978 MeRIP-seq:(Medium) rs1174991563 Functional Loss SNV dbSNP153 33..33 33 - - - 79316 RMVar_ID_79316 Human_SNP_ID_613782470 m1A Human chr16 + 88811621 88811621 88811621 GGTGTCGCGCCAGGAGGCCGATGGCGGCGCGGAAGGAGGCGGGGTCCTTCAGGACGGGCGAGATG GGTGTCGCGCCAGGAGGCCGATGGCGGCGCGGTAGGAGGCGGGGTCCTTCAGGACGGGCGAGATG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:88811504..88811975;chr16:88811524..88811701 26863196 MeRIP-seq:(Medium) rs749052990 Functional Loss SNV dbSNP153 33..33 33 - - - 79317 RMVar_ID_79317 Human_SNP_ID_613782487 m1A Human chr16 + 88811649 88811649 88811649 GCGGAAGGAGGCGGGGTCCTTCAGGACGGGCGAGATGTCCCTGGACCCAAGGACAGGCCTGGTGA GCGGAAGGAGGCGGGGTCCTTCAGGACGGGCGGGATGTCCCTGGACCCAAGGACAGGCCTGGTGA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:88811526..88811975 26863410 MeRIP-seq:(Medium) rs775833509 Functional Loss SNV dbSNP153 33..33 33 - - - 79318 RMVar_ID_79318 Human_SNP_ID_613782488 m1A Human chr16 - 88811652 88811652 88811652 GCGTCACCAGGCCTGTCCTTGGGTCCAGGGACATCTCGCCCGTCCTGAAGGACCCCGCCTCCTTC GCGTCACCAGGCCTGTCCTTGGGTCCAGGGACTTCTCGCCCGTCCTGAAGGACCCCGCCTCCTTC T A APRT Ensembl:ENSG00000198931 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88811604..88811900 26863196 MeRIP-seq:(Medium) rs763334808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394091,Human_RBP_ID_5316965,Human_RBP_ID_5361240,Human_RBP_ID_9325494,Human_RBP_ID_17653629,Human_RBP_ID_22653356,Human_RBP_ID_25236143 Human_Splice_Rec_1749954,Human_Splice_Rec_1749960,Human_Splice_Rec_1749966,Human_Splice_Rec_1749972,Human_Splice_Rec_1749976,Human_Splice_Rec_1749980,Human_Splice_Rec_1749984,Human_Splice_Rec_1749994 RMVar_hsa_circ_117544,RMVar_hsa_circ_180567,RMVar_hsa_circ_80891,RMVar_hsa_circ_180568 79319 RMVar_ID_79319 Human_SNP_ID_613782489 m1A Human chr16 - 88811652 88811652 88811652 GCGTCACCAGGCCTGTCCTTGGGTCCAGGGACATCTCGCCCGTCCTGAAGGACCCCGCCTCCTTC GCGTCACCAGGCCTGTCCTTGGGTCCAGGGACGTCTCGCCCGTCCTGAAGGACCCCGCCTCCTTC T C APRT Ensembl:ENSG00000198931 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:88811604..88811900 26863196 MeRIP-seq:(Medium) rs763334808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394091,Human_RBP_ID_5316965,Human_RBP_ID_5361240,Human_RBP_ID_9325494,Human_RBP_ID_17653629,Human_RBP_ID_22653356,Human_RBP_ID_25236143 Human_Splice_Rec_1749954,Human_Splice_Rec_1749960,Human_Splice_Rec_1749966,Human_Splice_Rec_1749972,Human_Splice_Rec_1749976,Human_Splice_Rec_1749980,Human_Splice_Rec_1749984,Human_Splice_Rec_1749994 RMVar_hsa_circ_117544,RMVar_hsa_circ_180567,RMVar_hsa_circ_80891,RMVar_hsa_circ_180568 79320 RMVar_ID_79320 Human_SNP_ID_613782492 m1A Human chr16 - 88811658 88811658 88811658 GCCCCGGCGTCACCAGGCCTGTCCTTGGGTCCAGGGACATCTCGCCCGTCCTGAAGGACCCCGCC GCCCCGGCGTCACCAGGCCTGTCCTTGGGTCCGGGGACATCTCGCCCGTCCTGAAGGACCCCGCC T C APRT Ensembl:ENSG00000198931 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:88811576..88811950 26863196 MeRIP-seq:(Medium) rs751779314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5316965,Human_RBP_ID_5361240,Human_RBP_ID_22652561 RMVar_hsa_circ_117544,RMVar_hsa_circ_180568 79321 RMVar_ID_79321 Human_SNP_ID_613782493 m1A Human chr16 - 88811658 88811658 88811658 GCCCCGGCGTCACCAGGCCTGTCCTTGGGTCCAGGGACATCTCGCCCGTCCTGAAGGACCCCGCC GCCCCGGCGTCACCAGGCCTGTCCTTGGGTCCCGGGACATCTCGCCCGTCCTGAAGGACCCCGCC T G APRT Ensembl:ENSG00000198931 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:88811576..88811950 26863196 MeRIP-seq:(Medium) rs751779314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5316965,Human_RBP_ID_5361240,Human_RBP_ID_22652561 RMVar_hsa_circ_117544,RMVar_hsa_circ_180568 79322 RMVar_ID_79322 Human_SNP_ID_613782843 m1A Human chr16 + 88812336 88812336 88812336 GCTGGCGCGCGGGGTGGAGAAGGGCGTGAGGAAGCGGTCCAAGTAGCAGGAGGGCGGTGCAGGGC GCTGGCGCGCGGGGTGGAGAAGGGCGTGAGGACGCGGTCCAAGTAGCAGGAGGGCGGTGCAGGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88812285..88812481 26863196 MeRIP-seq:(Medium) rs980590539 Functional Loss SNV dbSNP153 33..33 33 - - - 79323 RMVar_ID_79323 Human_SNP_ID_613782867 m1A Human chr16 + 88812377 88812377 88812377 AGTAGCAGGAGGGCGGTGCAGGGCCCGGAGGGAGCAGCCCAGGGCGGAGGCGGCGGGCCTGGGCT AGTAGCAGGAGGGCGGTGCAGGGCCCGGAGGGTGCAGCCCAGGGCGGAGGCGGCGGGCCTGGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88812326..88812505 26863196 MeRIP-seq:(Medium) rs1037507545 Functional Loss SNV dbSNP153 33..33 33 - - - 79324 RMVar_ID_79324 Human_SNP_ID_613783615 m1A Human chr16 + 88814267 88814267 88814267 AGGCGCCGTGGGCGAGGAGGAGGGCCAAGCACACGCCAGGGTCAGGTCCTGGGCAGGTGGAATTG AGGCGCCGTGGGCGAGGAGGAGGGCCAAGCACCCGCCAGGGTCAGGTCCTGGGCAGGTGGAATTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88814216..88814330 26863196 MeRIP-seq:(Medium) rs546528874 Functional Loss SNV dbSNP153 33..33 33 - - - 79325 RMVar_ID_79325 Human_SNP_ID_613783679 m1A Human chr16 - 88814423 88814423 88814423 GCCTCTGGTCCCACTAGCACCTGCGCAGACTCAGGCCAGGCCTAGAATCTCCGGTTGGCCCTGCA GCCTCTGGTCCCACTAGCACCTGCGCAGACTCCGGCCAGGCCTAGAATCTCCGGTTGGCCCTGCA T G GALNS Ensembl:ENSG00000141012 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:88814205..88814425 26863196 MeRIP-seq:(Medium) rs1430608874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128634,Human_RBP_ID_481661,Human_RBP_ID_18686873 79326 RMVar_ID_79326 Human_SNP_ID_613787529 m1A Human chr16 - 88825038 88825038 88825038 AGGAGCTCCAGCCCCGGCCGCCCAGGCACCCCAGCCCCAGCCACCTTGCGGGCCTTTTTACTTTT AGGAGCTCCAGCCCCGGCCGCCCAGGCACCCCCGCCCCAGCCACCTTGCGGGCCTTTTTACTTTT T G GALNS Ensembl:ENSG00000141012 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88825009..88825860 26863196 MeRIP-seq:(Medium) rs1464323289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102567,RMVar_hsa_circ_376987,RMVar_hsa_circ_320816,RMVar_hsa_circ_50460,RMVar_hsa_circ_180569,RMVar_hsa_circ_180570,RMVar_hsa_circ_109800,RMVar_hsa_circ_328334,RMVar_hsa_circ_352742,RMVar_hsa_circ_180571,RMVar_hsa_circ_376077,RMVar_hsa_circ_180572 79327 RMVar_ID_79327 Human_SNP_ID_613787550 m1A Human chr16 + 88825079 88825056 88825079 TGGGCGGCCGGGGCTGGAGCTCCTGGGTGGCCAGGGCTGGGGTGACTGGGTATCTGGGGCGCCTG TGGGCGGCCG_______________________GGGCTGGGGTGACTGGGTATCTGGGGCGCCTG GGGGCTGGAGCTCCTGGGTGGCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88825060..88825395 26863196 MeRIP-seq:(Medium) rs796942675 Functional Loss DEL dbSNP153 11..33 33 - - - 79328 RMVar_ID_79328 Human_SNP_ID_613787564 m1A Human chr16 + 88825079 88825079 88825079 TGGGCGGCCGGGGCTGGAGCTCCTGGGTGGCCAGGGCTGGGGTGACTGGGTATCTGGGGCGCCTG TGGGCGGCCGGGGCTGGAGCTCCTGGGTGGCCGGGGCTGGGGTGACTGGGTATCTGGGGCGCCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88825060..88825395 26863196 MeRIP-seq:(Medium) rs1327781720 Functional Loss SNV dbSNP153 33..33 33 - - - 79329 RMVar_ID_79329 Human_SNP_ID_613789999 m1A Human chr16 + 88831083 88831083 88831083 GACCACGGATGTCTCCTCACCACACAGTCATTACCAGCACCCACGTGACACACGGCAGTATACGT GACCACGGATGTCTCCTCACCACACAGTCATTGCCAGCACCCACGTGACACACGGCAGTATACGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88831049..88831250 26863196 MeRIP-seq:(Medium) rs1047966589 Functional Loss SNV dbSNP153 33..33 33 - - - 79330 RMVar_ID_79330 Human_SNP_ID_613790241 m1A Human chr16 + 88831819 88831819 88831819 GAGCGGTGAGGCCGAGCACGGGGAGCGTGGGGAGGAGGGTGGTGAGGCTGAGCATGGGGTGCGTG GAGCGGTGAGGCCGAGCACGGGGAGCGTGGGGGGGAGGGTGGTGAGGCTGAGCATGGGGTGCGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88831783..88831944;chr16:88831814..88831963 26863196 MeRIP-seq:(Medium) rs1425118038 Functional Loss SNV dbSNP153 33..33 33 - - - 79331 RMVar_ID_79331 Human_SNP_ID_613790245 m1A Human chr16 - 88831850 88831829 88831851 TCTCCTCCCCACGCACCCTGTGCTCAGCCTCCACGCACCCCATGCTCAGCCTCACCACCCTCCTC TCTCCTCCCCACGCACCCTGTGCTCAGCCTC______________________ACCACCCTCCTC TGAGGCTGAGCATGGGGTGCGTG T GALNS Ensembl:ENSG00000141012 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88831822..88831949 26863196 MeRIP-seq:(Medium) rs1219426717 Functional Loss DEL dbSNP153 32..53 33 - - - Human_RBP_ID_21971653,Human_RBP_ID_22474047 RMVar_hsa_circ_102567,RMVar_hsa_circ_376987,RMVar_hsa_circ_320816,RMVar_hsa_circ_50460,RMVar_hsa_circ_180569,RMVar_hsa_circ_180570,RMVar_hsa_circ_109800,RMVar_hsa_circ_352742,RMVar_hsa_circ_180571 79332 RMVar_ID_79332 Human_SNP_ID_613799764 m1A Human chr16 + 88856156 88856156 88856156 GCTGGCTGTGACCCCTGACCCCGCACTTGCCCACCAGGAGACATTCCAGCCTTTCAGTTCTTCAG GCTGGCTGTGACCCCTGACCCCGCACTTGCCCTCCAGGAGACATTCCAGCCTTTCAGTTCTTCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88856152..88856434 26863196 MeRIP-seq:(Medium) rs773753814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1750141 79333 RMVar_ID_79333 Human_SNP_ID_613800260 m1A Human chr16 + 88856908 88856908 88856908 ATGGCAACCACGGGAGCCGCGGAGCCCCGGCCAGCGAGCCGACCTAGCGAGCGTCCGCCGGCCCT ATGGCAACCACGGGAGCCGCGGAGCCCCGGCCGGCGAGCCGACCTAGCGAGCGTCCGCCGGCCCT A G TRAPPC2L Ensembl:ENSG00000167515 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:88856837..88856933 26863410 MeRIP-seq:(Medium) rs1234012961 Functional Loss SNV dbSNP153 33..33 33 - - - 79334 RMVar_ID_79334 Human_SNP_ID_613800467 m1A Human chr16 + 88857182 88857182 88857182 GATGGCGGTGTGCATCGCGGTGATTGCCAAGGAGGTGCGTACGCGCGGCGTGGGGCGTCCGGGCT GATGGCGGTGTGCATCGCGGTGATTGCCAAGGTGGTGCGTACGCGCGGCGTGGGGCGTCCGGGCT A T TRAPPC2L Ensembl:ENSG00000167515 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88857147..88857222 26863196 MeRIP-seq:(Medium) rs751136345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4389672,Human_RBP_ID_19072380 Human_Splice_Rec_1750151,Human_Splice_Rec_1750159,Human_Splice_Rec_1750167,Human_Splice_Rec_1750171,Human_Splice_Rec_1750177,Human_Splice_Rec_1750183,Human_Splice_Rec_1750191,Human_Splice_Rec_1750197,Human_Splice_Rec_1750205,Human_Splice_Rec_1750213 RMVar_hsa_circ_180575,RMVar_hsa_circ_106778 79335 RMVar_ID_79335 Human_SNP_ID_613801590 m1A Human chr16 + 88859918 88859918 88859918 TTTTCAGATGTTCCGGAAGCTACACAACTCCTACACAGACGTGATGTGCAACCCCTTCTACAACC TTTTCAGATGTTCCGGAAGCTACACAACTCCTTCACAGACGTGATGTGCAACCCCTTCTACAACC A T TRAPPC2L Ensembl:ENSG00000167515 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88859876..88860009 32194978 MeRIP-seq:(Medium) rs1298757265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17255661,Human_RBP_ID_17371569,Human_RBP_ID_26810739,Human_RBP_ID_27447214 Human_Splice_Rec_1750148,Human_Splice_Rec_1750149,Human_Splice_Rec_1750156,Human_Splice_Rec_1750157,Human_Splice_Rec_1750164,Human_Splice_Rec_1750165,Human_Splice_Rec_1750182,Human_Splice_Rec_1750188,Human_Splice_Rec_1750189,Human_Splice_Rec_1750194,Human_Splice_Rec_1750195,Human_Splice_Rec_1750202,Human_Splice_Rec_1750203,Human_Splice_Rec_1750210,Human_Splice_Rec_1750211,Human_Splice_Rec_1750218,Human_Splice_Rec_1750219,Human_Splice_Rec_1750224,Human_Splice_Rec_1750225,Human_Splice_Rec_1750227 RMVar_hsa_circ_180575,RMVar_hsa_circ_106778 79336 RMVar_ID_79336 Human_SNP_ID_613802629 m1A Human chr16 + 88862294 88862294 88862294 TAACAGAACCCCGGTGCCTCTGCCCAGTTCCAATAGCGGGCAGACGAGAGCCATGTCCTGGGCTC TAACAGAACCCCGGTGCCTCTGCCCAGTTCCAGTAGCGGGCAGACGAGAGCCATGTCCTGGGCTC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1442845003 Functional Loss SNV dbSNP153 33..33 33 - - - 79337 RMVar_ID_79337 Human_SNP_ID_613870530 m1A Human chr16 - 89045612 89045612 89045612 TTCACAAGAGCAGTGGCCCAGGGAGCGAGGGGAGAGACAGAAGGCTGGGCAGAGGCAGTCGGTCT TTCACAAGAGCAGTGGCCCAGGGAGCGAGGGGCGAGACAGAAGGCTGGGCAGAGGCAGTCGGTCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89045513..89045616 26863196 MeRIP-seq:(Medium) rs539218256 Functional Loss SNV dbSNP153 33..33 33 - - - 79338 RMVar_ID_79338 Human_SNP_ID_613870700 m1A Human chr16 + 89046096 89046096 89046096 TCATCATCACTATCACCATCACCACCATCCCCACAGTCATCACCATCCCTATCATCACCATCATC TCATCATCACTATCACCATCACCACCATCCCCGCAGTCATCACCATCCCTATCATCACCATCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89046020..89046127 26863196 MeRIP-seq:(Medium) rs564666923 Functional Loss SNV dbSNP153 33..33 33 - - - 79339 RMVar_ID_79339 Human_SNP_ID_613872301 m1A Human chr16 - 89051108 89051106 89051108 GCTGTGCTTCAGAGCTTCAGGGAAAGGCTCAGAGCCCCGCAGAGGCCCAGCCTGAGACATCCCGG GCTGTGCTTCAGAGCTTCAGGGAAAGGCTCAG__CCCCGCAGAGGCCCAGCCTGAGACATCCCGG GCT G AC135782.1 Ensembl:ENSG00000256982 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89051057..89051153 26863196 MeRIP-seq:(Medium) rs1332390897 Functional Loss DEL dbSNP153 33..34 33 - - - 79340 RMVar_ID_79340 Human_SNP_ID_613872552 m1A Human chr16 - 89051893 89051893 89051893 AGCAGGAGTGCGGGTGACGGTGCAGCAAGCCCAGCTGCTGAGGGTGGGAAGGAGCCCGAGGTGAG AGCAGGAGTGCGGGTGACGGTGCAGCAAGCCCTGCTGCTGAGGGTGGGAAGGAGCCCGAGGTGAG T A AC135782.1 Ensembl:ENSG00000256982 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89051857..89051944 26863196 MeRIP-seq:(Medium) rs117170799 Functional Loss SNV dbSNP153 33..33 33 - - - 79341 RMVar_ID_79341 Human_SNP_ID_613872987 m1A Human chr16 + 89052843 89052843 89052843 CCCCACCCCTGGCAACACACATCCCTCCTGTCAGGAGCAGACATAGCCAAGAAAGCCCAGAGCAG CCCCACCCCTGGCAACACACATCCCTCCTGTCGGGAGCAGACATAGCCAAGAAAGCCCAGAGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89052794..89052905 26863196 MeRIP-seq:(Medium) rs113409120 Functional Loss SNV dbSNP153 33..33 33 - - - 79342 RMVar_ID_79342 Human_SNP_ID_613889389 m1A Human chr16 + 89098640 89098640 89098640 CGGGTTCCAGCGCCAGGCCTGGTGCCTGCCCCAGGAGGATGAGCATTTGCATTGCCTGCACCTTA CGGGTTCCAGCGCCAGGCCTGGTGCCTGCCCCGGGAGGATGAGCATTTGCATTGCCTGCACCTTA A G ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89098548..89098723 26863196 MeRIP-seq:(Medium) rs1249872981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4395124,Human_RBP_ID_18686943 Human_Splice_Rec_1750384,Human_Splice_Rec_1750404,Human_Splice_Rec_1750474 Human_miRNA_ID_1940400,Human_miRNA_ID_2040983,Human_miRNA_ID_3019967,Human_miRNA_ID_3082807 RMVar_hsa_circ_275055,RMVar_hsa_circ_306618,RMVar_hsa_circ_329217,RMVar_hsa_circ_331682,RMVar_hsa_circ_301758,RMVar_hsa_circ_305640,RMVar_hsa_circ_279506,RMVar_hsa_circ_180580,RMVar_hsa_circ_180582,RMVar_hsa_circ_180583,RMVar_hsa_circ_180581,RMVar_hsa_circ_180579 79343 RMVar_ID_79343 Human_SNP_ID_613902922 m1A Human chr16 + 89137244 89137244 89137244 CTTAGAGAAGAGCCAGGGATCCCGGGAGGACCACCAGGAGCTTGTGGGGAAGGACTGAGGGGAAG CTTAGAGAAGAGCCAGGGATCCCGGGAGGACCGCCAGGAGCTTGTGGGGAAGGACTGAGGGGAAG A G ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89137238..89137400 26863196 MeRIP-seq:(Medium) rs986476492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329217,RMVar_hsa_circ_180579,RMVar_hsa_circ_91184,RMVar_hsa_circ_180586,RMVar_hsa_circ_54802,RMVar_hsa_circ_93018,RMVar_hsa_circ_180590 79344 RMVar_ID_79344 Human_SNP_ID_613902939 m1A Human chr16 - 89137321 89137266 89137321 GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCAATCCTTCCCCGTGAGCTCCTGGTGGTCCTCCCG GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCA_________________________________ CTGAGGGGAAGAGCCCCAGGTCTCGGGAGGACCACCAGGAGCTCACGGGGAAGGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89137271..89137364 26863196 MeRIP-seq:(Medium) rs1567733639 Functional Loss DEL dbSNP153 33..65 33 - - - 79345 RMVar_ID_79345 Human_SNP_ID_613902976 m1A Human chr16 - 89137321 89137321 89137321 GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCAATCCTTCCCCGTGAGCTCCTGGTGGTCCTCCCG GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCAGTCCTTCCCCGTGAGCTCCTGGTGGTCCTCCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89137271..89137364 26863196 MeRIP-seq:(Medium) rs1432743620 Functional Loss SNV dbSNP153 33..33 33 - - - 79346 RMVar_ID_79346 Human_SNP_ID_613902977 m1A Human chr16 - 89137321 89137321 89137321 GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCAATCCTTCCCCGTGAGCTCCTGGTGGTCCTCCCG GGTCCTCCCGAGACCCGGGGCTCTTCCCCTCACTCCTTCCCCGTGAGCTCCTGGTGGTCCTCCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89137271..89137364 26863196 MeRIP-seq:(Medium) rs1432743620 Functional Loss SNV dbSNP153 33..33 33 - - - 79347 RMVar_ID_79347 Human_SNP_ID_613903021 m1A Human chr16 - 89137563 89137398 89137563 TCCTTCCCCACGAGCTCCTGGTGGTCCTCCCGAGACCTGGGGCTCTTCCCCTCAATCTTTCCCCG TCCTTCCCCACGAGCTCCTGGTGGTCCTCCCG_________________________________ CCGGGAGGACCACCAGGAGCTCACGGGGAAGGATTGAGGGGAAGAGCCCCAGGTCTCGGGAGGACCACCAGGAGCTCACGGGGAAAGATTGAGGGGAAGAGCCCCAGGTCTCGGGAGGACCACCAGGAGCTCACGGGGAAAGATTGAGGGGAAGAGCCCCAGGTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89137552..89137696 26863196 MeRIP-seq:(Medium) rs34658923 Functional Loss DEL dbSNP153 33..65 33 - - - 79348 RMVar_ID_79348 Human_SNP_ID_613903091 m1A Human chr16 + 89137558 89137558 89137558 GCTCACGGGGAAAGATTGAGGGGAAGAGCCCCAGGTCTCGGGAGGACCACCAGGAGCTCGTGGGG GCTCACGGGGAAAGATTGAGGGGAAGAGCCCCGGGTCTCGGGAGGACCACCAGGAGCTCGTGGGG A G ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89137556..89137676 26863196 MeRIP-seq:(Medium) rs35202828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329217,RMVar_hsa_circ_180579,RMVar_hsa_circ_91184,RMVar_hsa_circ_180586,RMVar_hsa_circ_54802,RMVar_hsa_circ_93018,RMVar_hsa_circ_180590 79349 RMVar_ID_79349 Human_SNP_ID_613903093 m1A Human chr16 - 89137563 89137563 89137563 TCCTTCCCCACGAGCTCCTGGTGGTCCTCCCGAGACCTGGGGCTCTTCCCCTCAATCTTTCCCCG TCCTTCCCCACGAGCTCCTGGTGGTCCTCCCGGGACCTGGGGCTCTTCCCCTCAATCTTTCCCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89137552..89137696 26863196 MeRIP-seq:(Medium) rs35209748 Functional Loss SNV dbSNP153 33..33 33 - - - 79350 RMVar_ID_79350 Human_SNP_ID_613906174 m1A Human chr16 + 89146343 89146343 89146343 CGGCCTGTGGTGGGTTCCGTCCTGGTCCCAGGAGAGATCCCGGATGAGCCAGGCCAGGCCCATGC CGGCCTGTGGTGGGTTCCGTCCTGGTCCCAGGGGAGATCCCGGATGAGCCAGGCCAGGCCCATGC A G ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89146340..89146536 32194978 MeRIP-seq:(Medium) rs571285741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262166 79351 RMVar_ID_79351 Human_SNP_ID_613936130 m1A Human chr16 + 89222866 89222865 89222867 AGTGCCCAGTGAGCGTGGTGAGAGAAGCTCACATGTTAGAGGTGTCGTTGCGGCCGTGTGACTGG AGTGCCCAGTGAGCGTGGTGAGAGAAGCTCAC__GTTAGAGGTGTCGTTGCGGCCGTGTGACTGG CAT C ZNF778 Ensembl:ENSG00000170100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89222815..89223060 26863196 MeRIP-seq:(Medium) rs984796659 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_60847,RMVar_hsa_circ_279646,RMVar_hsa_circ_180596 79352 RMVar_ID_79352 Human_SNP_ID_613936131 m1A Human chr16 + 89222866 89222866 89222866 AGTGCCCAGTGAGCGTGGTGAGAGAAGCTCACATGTTAGAGGTGTCGTTGCGGCCGTGTGACTGG AGTGCCCAGTGAGCGTGGTGAGAGAAGCTCACGTGTTAGAGGTGTCGTTGCGGCCGTGTGACTGG A G ZNF778 Ensembl:ENSG00000170100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89222815..89223060 26863196 MeRIP-seq:(Medium) rs1165102161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60847,RMVar_hsa_circ_279646,RMVar_hsa_circ_180596 79353 RMVar_ID_79353 Human_SNP_ID_613936160 m1A Human chr16 + 89222908 89222907 89222909 TGTCGTTGCGGCCGTGTGACTGGAGGAGAGCGACAGGGTGCGCGTGACTGGAGGAGCGCGACAGG TGTCGTTGCGGCCGTGTGACTGGAGGAGAGCG__AGGGTGCGCGTGACTGGAGGAGCGCGACAGG GAC G ZNF778 Ensembl:ENSG00000170100 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89222859..89222966 26863196 MeRIP-seq:(Medium) rs200850266 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5647380 RMVar_hsa_circ_60847,RMVar_hsa_circ_279646,RMVar_hsa_circ_180596 79354 RMVar_ID_79354 Human_SNP_ID_613936172 m1A Human chr16 - 89222914 89222914 89222914 GCGTGCCCTGTCGCGCTCCTCCAGTCACGCGCACCCTGTCGCTCTCCTCCAGTCACACGGCCGCA GCGTGCCCTGTCGCGCTCCTCCAGTCACGCGCTCCCTGTCGCTCTCCTCCAGTCACACGGCCGCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89222830..89223041 26863196 MeRIP-seq:(Medium) rs932030298 Functional Loss SNV dbSNP153 33..33 33 - - - 79355 RMVar_ID_79355 Human_SNP_ID_613936173 m1A Human chr16 - 89222914 89222914 89222914 GCGTGCCCTGTCGCGCTCCTCCAGTCACGCGCACCCTGTCGCTCTCCTCCAGTCACACGGCCGCA GCGTGCCCTGTCGCGCTCCTCCAGTCACGCGCGCCCTGTCGCTCTCCTCCAGTCACACGGCCGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89222830..89223041 26863196 MeRIP-seq:(Medium) rs932030298 Functional Loss SNV dbSNP153 33..33 33 - - - 79356 RMVar_ID_79356 Human_SNP_ID_613945738 m1A Human chr16 + 89243188 89243188 89243188 GGAGGAGAAGACAGTGTTGACCTGGGGCGTTGAGGGATGAGGAGTCCTGTAGGCAGCAGTGGAAA GGAGGAGAAGACAGTGTTGACCTGGGGCGTTGGGGGATGAGGAGTCCTGTAGGCAGCAGTGGAAA A G HSALNG0113594 RNACentral:URS0000EB170F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89243137..89243211 26863196 MeRIP-seq:(Medium) rs1317626013 Functional Loss SNV dbSNP153 33..33 33 - - - 79357 RMVar_ID_79357 Human_SNP_ID_613945739 m1A Human chr16 + 89243188 89243188 89243188 GGAGGAGAAGACAGTGTTGACCTGGGGCGTTGAGGGATGAGGAGTCCTGTAGGCAGCAGTGGAAA GGAGGAGAAGACAGTGTTGACCTGGGGCGTTGTGGGATGAGGAGTCCTGTAGGCAGCAGTGGAAA A T HSALNG0113594 RNACentral:URS0000EB170F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89243137..89243211 26863196 MeRIP-seq:(Medium) rs1317626013 Functional Loss SNV dbSNP153 33..33 33 - - - 79358 RMVar_ID_79358 Human_SNP_ID_613961065 m1A Human chr16 - 89280498 89280498 89280498 CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTACCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTGCCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89280423..89280669 26863196 MeRIP-seq:(Medium) rs770628197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371570,Human_RBP_ID_22715540,Human_RBP_ID_27447325 Human_miRNA_ID_167063,Human_miRNA_ID_464597,Human_miRNA_ID_2147114,Human_miRNA_ID_2387186,Human_miRNA_ID_2388659,Human_miRNA_ID_2390896,Human_miRNA_ID_2399807,Human_miRNA_ID_2592142,Human_miRNA_ID_2988539,Human_miRNA_ID_3022240,Human_miRNA_ID_3030864 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79359 RMVar_ID_79359 Human_SNP_ID_613961066 m1A Human chr16 - 89280498 89280498 89280498 CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTACCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTCCCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89280423..89280669 26863196 MeRIP-seq:(Medium) rs770628197 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17371570,Human_RBP_ID_22715540,Human_RBP_ID_27447325 Human_miRNA_ID_167063,Human_miRNA_ID_464597,Human_miRNA_ID_2147114,Human_miRNA_ID_2387186,Human_miRNA_ID_2388659,Human_miRNA_ID_2390896,Human_miRNA_ID_2399807,Human_miRNA_ID_2592142,Human_miRNA_ID_2988539,Human_miRNA_ID_3022240,Human_miRNA_ID_3030864 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79360 RMVar_ID_79360 Human_SNP_ID_613961067 m1A Human chr16 + 89280499 89280499 89280499 GTACGGGGCAGGAGAGGCGGGAGGGGCGGGGTACGGCGCCTCCGAGGCGCTGAAGGGCCCTGGGG GTACGGGGCAGGAGAGGCGGGAGGGGCGGGGTGCGGCGCCTCCGAGGCGCTGAAGGGCCCTGGGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89280453..89280600 26863196 MeRIP-seq:(Medium) rs1395480845 Functional Loss SNV dbSNP153 33..33 33 - - - 79361 RMVar_ID_79361 Human_SNP_ID_613961104 m1A Human chr16 + 89280536 89280536 89280536 GCCTCCGAGGCGCTGAAGGGCCCTGGGGCGGCAGAGTGGAGGGGGTCCGCGGGGCAGAAACGCTT GCCTCCGAGGCGCTGAAGGGCCCTGGGGCGGCGGAGTGGAGGGGGTCCGCGGGGCAGAAACGCTT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89280476..89280550 26863196 MeRIP-seq:(Medium) rs1170877791 Functional Loss SNV dbSNP153 33..33 33 - - - 79362 RMVar_ID_79362 Human_SNP_ID_613961105 m1A Human chr16 + 89280536 89280536 89280536 GCCTCCGAGGCGCTGAAGGGCCCTGGGGCGGCAGAGTGGAGGGGGTCCGCGGGGCAGAAACGCTT GCCTCCGAGGCGCTGAAGGGCCCTGGGGCGGCCGAGTGGAGGGGGTCCGCGGGGCAGAAACGCTT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89280476..89280550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 79363 RMVar_ID_79363 Human_SNP_ID_613961161 m1A Human chr16 + 89280603 89280603 89280603 GGGACTCGGGGAATCTCTGTGGAGACTTCAGCAGGAGGTCCGAGCCCACAGGCCAGCTCACAGGG GGGACTCGGGGAATCTCTGTGGAGACTTCAGCGGGAGGTCCGAGCCCACAGGCCAGCTCACAGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89280553..89280704 32194978 MeRIP-seq:(Medium) rs763152116 Functional Loss SNV dbSNP153 33..33 33 - - - 79364 RMVar_ID_79364 Human_SNP_ID_613961410 m1A Human chr16 + 89280967 89280967 89280967 CGGTGGGCAGTGCAAAGCGTCGACTTTGGGCGACGGGAGGCCATAGTCTGGGGAGTAGTACCCTG CGGTGGGCAGTGCAAAGCGTCGACTTTGGGCGGCGGGAGGCCATAGTCTGGGGAGTAGTACCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89280918..89281052 26863196 MeRIP-seq:(Medium) rs1318992601 Functional Loss SNV dbSNP153 33..33 33 - - - 79365 RMVar_ID_79365 Human_SNP_ID_613961630 m1A Human chr16 - 89281285 89281285 89281285 CGCAGCACTCCACGCCCGTGCCCACCGCTCCCACCAGCGCCTGCTCCCCCTCCTTTTTCGACAGG CGCAGCACTCCACGCCCGTGCCCACCGCTCCCGCCAGCGCCTGCTCCCCCTCCTTTTTCGACAGG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89281237..89281372 26863196 MeRIP-seq:(Medium) rs878921394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_464600,Human_miRNA_ID_2052373 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79366 RMVar_ID_79366 Human_SNP_ID_613961675 m1A Human chr16 - 89281347 89281347 89281347 GCCCAGGACCCCGTCCTGCAGCGCCGATGACTACGCGGACCTCGTGTTCGACTGCGCCGACTCGC GCCCAGGACCCCGTCCTGCAGCGCCGATGACTGCGCGGACCTCGTGTTCGACTGCGCCGACTCGC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89281326..89281350 26863196 MeRIP-seq:(Medium) rs1365408100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4389963,Human_RBP_ID_8811134,Human_RBP_ID_18687101 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79367 RMVar_ID_79367 Human_SNP_ID_613961936 m1A Human chr16 - 89281746 89281746 89281746 CCAGAAGGACCTGGAGATCGAGGAGCGCCACAAGCGGCACAAGGAGAGGATGAAGCAAATGGAGA CCAGAAGGACCTGGAGATCGAGGAGCGCCACAGGCGGCACAAGGAGAGGATGAAGCAAATGGAGA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr16:89281626..89282213;chr16:89281626..89282116 26863196 MeRIP-seq:(Medium) rs1567567505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45241,Human_RBP_ID_5524754,Human_RBP_ID_22715550,Human_RBP_ID_24544431,Human_RBP_ID_26329405,Human_RBP_ID_26769252,Human_RBP_ID_27560630 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79368 RMVar_ID_79368 Human_SNP_ID_613961986 m1A Human chr16 - 89281884 89281884 89281884 GGGCGACCCAGTGAAGATGAGCAACGGGAATGATAAGGTAGCGCCATCCAAAGACCCAGGCAAGA GGGCGACCCAGTGAAGATGAGCAACGGGAATGGTAAGGTAGCGCCATCCAAAGACCCAGGCAAGA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89281573..89282209;chr16:89281503..89282537 26863196 MeRIP-seq:(Medium) rs749585833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889106,Human_RBP_ID_2489839,Human_RBP_ID_4389993,Human_RBP_ID_5524755,Human_RBP_ID_9373375,Human_RBP_ID_26329406,Human_RBP_ID_27572452,Human_RBP_ID_27811333 Human_miRNA_ID_2565565,Human_miRNA_ID_2975794 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79369 RMVar_ID_79369 Human_SNP_ID_613962001 m1A Human chr16 - 89281917 89281917 89281917 GGAGAAATTCAAGGACGGTGCAGAGAAAGAAAAGGGCGACCCAGTGAAGATGAGCAACGGGAATG GGAGAAATTCAAGGACGGTGCAGAGAAAGAAAGGGGCGACCCAGTGAAGATGAGCAACGGGAATG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89281614..89281950 26863196 MeRIP-seq:(Medium) rs1383324924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889106,Human_RBP_ID_6546044,Human_RBP_ID_8442248,Human_RBP_ID_12847851,Human_RBP_ID_22053612,Human_RBP_ID_26329406,Human_RBP_ID_27811333 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79370 RMVar_ID_79370 Human_SNP_ID_613962091 m1A Human chr16 - 89282079 89282079 89282079 GGACAGGCATGCGGATGGGCTGCTGCGGCATCACAGGGACGAGCTCCTGCGGCATCACAGGGACG GGACAGGCATGCGGATGGGCTGCTGCGGCATCCCAGGGACGAGCTCCTGCGGCATCACAGGGACG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89282020..89282250 26863196 MeRIP-seq:(Medium) rs1024994586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4390003,Human_RBP_ID_5524756,Human_RBP_ID_6546045,Human_RBP_ID_8811153,Human_RBP_ID_9373376,Human_RBP_ID_17691021,Human_RBP_ID_17882722,Human_RBP_ID_19028622,Human_RBP_ID_22054354,Human_RBP_ID_22712705,Human_RBP_ID_24544433,Human_RBP_ID_26329407,Human_RBP_ID_26952211,Human_RBP_ID_27447357,Human_RBP_ID_27572716,Human_RBP_ID_27812059 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79371 RMVar_ID_79371 Human_SNP_ID_613962531 m1A Human chr16 - 89282916 89282916 89282916 AGAGAAAGTCTTTGAAAAGCACAAGGAGAAGAAGGATAAAGAGTCCACAGAAAAGTACAAGGACA AGAGAAAGTCTTTGAAAAGCACAAGGAGAAGACGGATAAAGAGTCCACAGAAAAGTACAAGGACA T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89282701..89283230 26863196 MeRIP-seq:(Medium) rs200223557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2489847,Human_RBP_ID_22003763 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79372 RMVar_ID_79372 Human_SNP_ID_613962575 m1A Human chr16 - 89283009 89283009 89283009 TTCTGACAAGCAGCACCCTGAGAGGCAGAAGGACAAGGAGCCCAGAGACAGGAGAAAGGACCGAG TTCTGACAAGCAGCACCCTGAGAGGCAGAAGGGCAAGGAGCCCAGAGACAGGAGAAAGGACCGAG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89282743..89283378 26863196 MeRIP-seq:(Medium) rs1447641697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5524758,Human_RBP_ID_24544439 Human_miRNA_ID_2425195,Human_miRNA_ID_2434857 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79373 RMVar_ID_79373 Human_SNP_ID_613962723 m1A Human chr16 + 89283359 89283359 89283359 TTGCCATGTGTGTCTTTATGTTTTTCCTTGGTATCTTTTTTCTCTTTAAAACATTTATCAAATTC TTGCCATGTGTGTCTTTATGTTTTTCCTTGGTGTCTTTTTTCTCTTTAAAACATTTATCAAATTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89283310..89283378 26863196 MeRIP-seq:(Medium) rs578006359 Functional Loss SNV dbSNP153 33..33 33 - - - 79374 RMVar_ID_79374 Human_SNP_ID_613962724 m1A Human chr16 + 89283359 89283359 89283359 TTGCCATGTGTGTCTTTATGTTTTTCCTTGGTATCTTTTTTCTCTTTAAAACATTTATCAAATTC TTGCCATGTGTGTCTTTATGTTTTTCCTTGGTTTCTTTTTTCTCTTTAAAACATTTATCAAATTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89283310..89283378 26863196 MeRIP-seq:(Medium) rs578006359 Functional Loss SNV dbSNP153 33..33 33 - - - 79375 RMVar_ID_79375 Human_SNP_ID_613962795 m1A Human chr16 - 89283527 89283527 89283527 AAGGGCCTGGAGCCGTGGGAACGGCACCACCCAGCACGAGAGAAGGAGAAGAAGGATGGCCCCGA AAGGGCCTGGAGCCGTGGGAACGGCACCACCCGGCACGAGAGAAGGAGAAGAAGGATGGCCCCGA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:89283501..89283800 26863196 MeRIP-seq:(Medium) rs1356574465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5524760,Human_RBP_ID_22053622,Human_RBP_ID_22715556,Human_RBP_ID_22802579,Human_RBP_ID_22944731,Human_RBP_ID_24544441,Human_RBP_ID_26329415,Human_RBP_ID_27572460 Human_miRNA_ID_1357097,Human_miRNA_ID_1549529,Human_miRNA_ID_1549810,Human_miRNA_ID_1550039,Human_miRNA_ID_3118600 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79376 RMVar_ID_79376 Human_SNP_ID_613962869 m1A Human chr16 - 89283649 89283649 89283649 CCCTGGAGAGCTGCAAGGAGCGCAGGGACGGCAGGGCCAAGCCCGAGGAGGCGCACCGGGAGGAG CCCTGGAGAGCTGCAAGGAGCGCAGGGACGGCCGGGCCAAGCCCGAGGAGGCGCACCGGGAGGAG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89283438..89283962 26863196 MeRIP-seq:(Medium) rs764389320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8812158,Human_RBP_ID_17652811,Human_RBP_ID_22712715,Human_RBP_ID_23118529,Human_RBP_ID_24544442,Human_RBP_ID_26329416 Human_miRNA_ID_864605,Human_miRNA_ID_2381265,Human_miRNA_ID_2579920 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79377 RMVar_ID_79377 Human_SNP_ID_613963444 m1A Human chr16 - 89284965 89284965 89284965 CAGCTCCCTCTCTGCCTCCTCCACCTCGTCTCACGGGAGCTCTGCCGCCCAGAAGCAGAACCCCA CAGCTCCCTCTCTGCCTCCTCCACCTCGTCTCTCGGGAGCTCTGCCGCCCAGAAGCAGAACCCCA T A ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89284653..89285104 32194978 MeRIP-seq:(Medium) rs374369335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45252,Human_RBP_ID_5465615,Human_RBP_ID_8442262,Human_RBP_ID_8811225,Human_RBP_ID_9286013,Human_RBP_ID_9373389,Human_RBP_ID_22054362,Human_RBP_ID_22713835,Human_RBP_ID_24544654,Human_RBP_ID_26330405,Human_RBP_ID_27447363,Human_RBP_ID_27572730,Human_RBP_ID_27812069 Human_miRNA_ID_1157592 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79378 RMVar_ID_79378 Human_SNP_ID_613963582 m1A Human chr16 - 89285252 89285252 89285252 GTGGGGACAGGAGAGAAGCTGAGACTCTCGGCACATACGATATTGCCTGGTAGTAAGACACGAGA GTGGGGACAGGAGAGAAGCTGAGACTCTCGGCGCATACGATATTGCCTGGTAGTAAGACACGAGA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89285203..89286193 32194978 MeRIP-seq:(Medium) rs766661580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005928,Human_RBP_ID_8811232,Human_RBP_ID_17882734,Human_RBP_ID_22712719,Human_RBP_ID_26330408 Human_miRNA_ID_2658812 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 79379 RMVar_ID_79379 Human_SNP_ID_613964723 m1A Human chr16 - 89288587 89288587 89288587 AGCAGCTGCTGGCTGCAGGTGCGGAGGTGAACACCAAGGGCCTAGATGACGACACGCCTTTGCAC AGCAGCTGCTGGCTGCAGGTGCGGAGGTGAACCCCAAGGGCCTAGATGACGACACGCCTTTGCAC T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89288480..89288696 26863196 MeRIP-seq:(Medium) rs1416356673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45260,Human_RBP_ID_1525208,Human_RBP_ID_4390215,Human_RBP_ID_8811251,Human_RBP_ID_9286017,Human_RBP_ID_9374861,Human_RBP_ID_17882745,Human_RBP_ID_18687174,Human_RBP_ID_27838036 Human_Splice_Rec_1750730,Human_Splice_Rec_1750731,Human_Splice_Rec_1750754,Human_Splice_Rec_1750755,Human_Splice_Rec_1750774,Human_Splice_Rec_1750775,Human_Splice_Rec_1750796,Human_Splice_Rec_1750797,Human_Splice_Rec_1750820,Human_Splice_Rec_1750821,Human_Splice_Rec_1750833,Human_Splice_Rec_1750848,Human_Splice_Rec_1750849,Human_Splice_Rec_1750854,Human_Splice_Rec_1750860,Human_Splice_Rec_1750861,Human_Splice_Rec_1750865,Human_Splice_Rec_1750880,Human_Splice_Rec_1750881,Human_Splice_Rec_1750904,Human_Splice_Rec_1750920,Human_Splice_Rec_1750921,Human_Splice_Rec_1750932,Human_Splice_Rec_1750944,Human_Splice_Rec_1750958,Human_Splice_Rec_1750968,Human_Splice_Rec_1750982,Human_Splice_Rec_1750994,Human_Splice_Rec_1750995,Human_Splice_Rec_1751010 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_34833,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180609 79380 RMVar_ID_79380 Human_SNP_ID_613965330 m1A Human chr16 + 89290322 89290322 89290322 AGCCGGGGGAGGCTCAGGGCTCCAATGGGGGGAGGCTCAGGGCTCCAGCGGGGGAGGCTCAGGGC AGCCGGGGGAGGCTCAGGGCTCCAATGGGGGGGGGCTCAGGGCTCCAGCGGGGGAGGCTCAGGGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89290318..89290542 26863196 MeRIP-seq:(Medium) rs1312491736 Functional Loss SNV dbSNP153 33..33 33 - - - 79381 RMVar_ID_79381 Human_SNP_ID_613966352 m1A Human chr16 - 89293442 89293442 89293442 GCCACAACTCTGCCCCAGCTCCTCCCTCCGCAACCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA GCCACAACTCTGCCCCAGCTCCTCCCTCCGCAGCCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:89293438..89293679;chr16:89293439..89293760 26863196 MeRIP-seq:(Medium) rs879457112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505851,Human_RBP_ID_17077738 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 79382 RMVar_ID_79382 Human_SNP_ID_613966353 m1A Human chr16 - 89293442 89293442 89293442 GCCACAACTCTGCCCCAGCTCCTCCCTCCGCAACCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA GCCACAACTCTGCCCCAGCTCCTCCCTCCGCACCCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA T G ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:89293438..89293679;chr16:89293439..89293760 26863196 MeRIP-seq:(Medium) rs879457112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505851,Human_RBP_ID_17077738 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 79383 RMVar_ID_79383 Human_SNP_ID_613967078 m1A Human chr16 - 89295706 89295706 89295706 CCCCCCATCCCACCTGCACAGAGCCAGGTGCCACCGCCGTTTGCCTCGGGACGCTCGCCTCCAGT CCCCCCATCCCACCTGCACAGAGCCAGGTGCCTCCGCCGTTTGCCTCGGGACGCTCGCCTCCAGT T A ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89295699..89295925 26863196 MeRIP-seq:(Medium) rs1295343854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2489919,Human_RBP_ID_24370053 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 79384 RMVar_ID_79384 Human_SNP_ID_613967081 m1A Human chr16 + 89295710 89295710 89295710 GAGGCGAGCGTCCCGAGGCAAACGGCGGTGGCACCTGGCTCTGTGCAGGTGGGATGGGGGGGATG GAGGCGAGCGTCCCGAGGCAAACGGCGGTGGCTCCTGGCTCTGTGCAGGTGGGATGGGGGGGATG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89295706..89295961 26863196 MeRIP-seq:(Medium) rs1036377800 Functional Loss SNV dbSNP153 33..33 33 - - - 79385 RMVar_ID_79385 Human_SNP_ID_613967093 m1A Human chr16 + 89295740 89295740 89295740 GCACCTGGCTCTGTGCAGGTGGGATGGGGGGGATGTGACGCGCCTGGGGGTGCCCTGTGCTGGTG GCACCTGGCTCTGTGCAGGTGGGATGGGGGGGCTGTGACGCGCCTGGGGGTGCCCTGTGCTGGTG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89295732..89295881 26863196 MeRIP-seq:(Medium) rs1467407554 Functional Loss SNV dbSNP153 33..33 33 - - - 79386 RMVar_ID_79386 Human_SNP_ID_613967094 m1A Human chr16 + 89295740 89295740 89295740 GCACCTGGCTCTGTGCAGGTGGGATGGGGGGGATGTGACGCGCCTGGGGGTGCCCTGTGCTGGTG GCACCTGGCTCTGTGCAGGTGGGATGGGGGGGGTGTGACGCGCCTGGGGGTGCCCTGTGCTGGTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89295732..89295881 26863196 MeRIP-seq:(Medium) rs1467407554 Functional Loss SNV dbSNP153 33..33 33 - - - 79387 RMVar_ID_79387 Human_SNP_ID_613967321 m1A Human chr16 - 89296325 89296325 89296325 AACAGGCACCTCGGCAGAGGAGAGAGCAGGGCAGGGAGACGGTGGCTCCAGAGGCCGGCAGCAGA AACAGGCACCTCGGCAGAGGAGAGAGCAGGGCCGGGAGACGGTGGCTCCAGAGGCCGGCAGCAGA T G ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89296321..89296413 26863196 MeRIP-seq:(Medium) rs1255764124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17206303,Human_RBP_ID_22712724,Human_RBP_ID_23274830,Human_RBP_ID_26329432 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 79388 RMVar_ID_79388 Human_SNP_ID_613968336 m1A Human chr16 - 89299469 89299469 89299469 CACACAGGGCACAGACCCCACACACCCCACACAGGGCAGGCACCTCACACAGGGCACAGACCCCA CACACAGGGCACAGACCCCACACACCCCACACGGGGCAGGCACCTCACACAGGGCACAGACCCCA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89299467..89300146 26863196 MeRIP-seq:(Medium) rs879401186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 79389 RMVar_ID_79389 Human_SNP_ID_613970347 m1A Human chr16 + 89305307 89305307 89305307 CCCTCACCTCCTTCCCGCCATCGCCACGCTCCAGTTTTGGGGTCTTGGTTAGAGAAACTTTATCT CCCTCACCTCCTTCCCGCCATCGCCACGCTCCGGTTTTGGGGTCTTGGTTAGAGAAACTTTATCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:89305201..89305367;chr16:89305158..89313345;chr16:89305201..89305378 26863196 MeRIP-seq:(Medium) rs750092547 Functional Loss SNV dbSNP153 33..33 33 - - - 79390 RMVar_ID_79390 Human_SNP_ID_613970597 m1A Human chr16 + 89305777 89305777 89305777 ACCTCCCACTCCGCAGACACGCGCCACCTCCCACTCCGCAGACACGCGCCACCTCCCACTCCGCA ACCTCCCACTCCGCAGACACGCGCCACCTCCCTCTCCGCAGACACGCGCCACCTCCCACTCCGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89305774..89305904 26863196 MeRIP-seq:(Medium) rs1261596143 Functional Loss SNV dbSNP153 33..33 33 - - - 79391 RMVar_ID_79391 Human_SNP_ID_613970926 m1A Human chr16 - 89306607 89306607 89306607 CGGAGTGGGAGGTAGGTGGCGCGTGTCTGCGGAGTGGGAGGTGGCGCGTGTCTGCGGAGTGGGAG CGGAGTGGGAGGTAGGTGGCGCGTGTCTGCGGGGTGGGAGGTGGCGCGTGTCTGCGGAGTGGGAG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:89306578..89306730 26863196 MeRIP-seq:(Medium) rs1331386807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180613,RMVar_hsa_circ_279522,RMVar_hsa_circ_321062,RMVar_hsa_circ_325779,RMVar_hsa_circ_277069,RMVar_hsa_circ_180612 79392 RMVar_ID_79392 Human_SNP_ID_613970929 m1A Human chr16 + 89306623 89306620 89306624 ACGCGCCACCTCCCACTCCGCAGACACGCGCCACCTACCTCCCACTCCGCAGACACGCACCACCT ACGCGCCACCTCCCACTCCGCAGACACGCG____CTACCTCCCACTCCGCAGACACGCACCACCT GCCAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89306619..89306717 26863196 MeRIP-seq:(Medium) rs199725798 Functional Loss DEL dbSNP153 31..34 33 - - - 79393 RMVar_ID_79393 Human_SNP_ID_613970930 m1A Human chr16 - 89306626 89306622 89306626 GGGAGGTGGTGCGTGTCTGCGGAGTGGGAGGTAGGTGGCGCGTGTCTGCGGAGTGGGAGGTGGCG GGGAGGTGGTGCGTGTCTGCGGAGTGGGAGGT____GGCGCGTGTCTGCGGAGTGGGAGGTGGCG CACCT C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89306614..89306732 26863196 MeRIP-seq:(Medium) rs200555542 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180613,RMVar_hsa_circ_279522,RMVar_hsa_circ_321062,RMVar_hsa_circ_325779,RMVar_hsa_circ_277069,RMVar_hsa_circ_180612 79394 RMVar_ID_79394 Human_SNP_ID_613970933 m1A Human chr16 - 89306626 89306626 89306626 GGGAGGTGGTGCGTGTCTGCGGAGTGGGAGGTAGGTGGCGCGTGTCTGCGGAGTGGGAGGTGGCG GGGAGGTGGTGCGTGTCTGCGGAGTGGGAGGTGGGTGGCGCGTGTCTGCGGAGTGGGAGGTGGCG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89306614..89306732 26863196 MeRIP-seq:(Medium) rs1398593961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180613,RMVar_hsa_circ_279522,RMVar_hsa_circ_321062,RMVar_hsa_circ_325779,RMVar_hsa_circ_277069,RMVar_hsa_circ_180612 79395 RMVar_ID_79395 Human_SNP_ID_613971042 m1A Human chr16 + 89306821 89306786 89306821 ACCTCCCACTCCGCAGACACGCGCCACCTCCCATTCCACAGACACGCGCCACTTACCTCCCACTC _________________________________TTCCACAGACACGCGCCACTTACCTCCCACTC CCTACCTCCCACTCCGCAGACACGCGCCACCTCCCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89306808..89306899 26863196 MeRIP-seq:(Medium) rs1206645410 Functional Loss DEL dbSNP153 1..33 33 - - - 79396 RMVar_ID_79396 Human_SNP_ID_613971049 m1A Human chr16 + 89306821 89306797 89306822 ACCTCCCACTCCGCAGACACGCGCCACCTCCCATTCCACAGACACGCGCCACTTACCTCCCACTC ACCTCCCAC_________________________TCCACAGACACGCGCCACTTACCTCCCACTC CTCCGCAGACACGCGCCACCTCCCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89306808..89306899 26863196 MeRIP-seq:(Medium) rs1567617510 Functional Loss DEL dbSNP153 10..34 33 - - - 79397 RMVar_ID_79397 Human_SNP_ID_613973683 m1A Human chr16 - 89314522 89314520 89314522 ACGAGACGAGAAAGGCCGGAAGAGCCACAGAGAGCAGGTCGTGTTGGCGCAGGAGGCAGGGTGTC ACGAGACGAGAAAGGCCGGAAGAGCCACAGAG__CAGGTCGTGTTGGCGCAGGAGGCAGGGTGTC GCT G ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89314520..89314668 26863196 MeRIP-seq:(Medium) rs1447284116 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_815672 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180613,RMVar_hsa_circ_279522,RMVar_hsa_circ_325779,RMVar_hsa_circ_277069,RMVar_hsa_circ_180612,RMVar_hsa_circ_31494 79398 RMVar_ID_79398 Human_SNP_ID_613983074 m1A Human chr16 + 89342002 89341960 89342002 AGGAGTGCTGCACCTCCACCCACAGCGGCCACAGCCCACGGCGGGAGTGCTGCACCTCCACTGCC _________________________________GCCCACGGCGGGAGTGCTGCACCTCCACTGCC GGCCCATGGCAGGAGTGCTGCACCTCCACCCACAGCGGCCACA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89342001..89342113 26863196 MeRIP-seq:(Medium) rs1567673952 Functional Loss DEL dbSNP153 1..33 33 - - - 79399 RMVar_ID_79399 Human_SNP_ID_613983108 m1A Human chr16 + 89342002 89342002 89342002 AGGAGTGCTGCACCTCCACCCACAGCGGCCACAGCCCACGGCGGGAGTGCTGCACCTCCACTGCC AGGAGTGCTGCACCTCCACCCACAGCGGCCACGGCCCACGGCGGGAGTGCTGCACCTCCACTGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89342001..89342113 26863196 MeRIP-seq:(Medium) rs167956 Functional Loss SNV dbSNP153 33..33 33 - - - 79400 RMVar_ID_79400 Human_SNP_ID_613989228 m1A Human chr16 + 89361064 89361064 89361064 GGCAGCCCTGGGCTCCAGGATCAGCCCACCCCAGCCCCTGCTGCAATGGCACCTCCTACTCTCAT GGCAGCCCTGGGCTCCAGGATCAGCCCACCCCCGCCCCTGCTGCAATGGCACCTCCTACTCTCAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89361060..89361197 26863196 MeRIP-seq:(Medium) rs1326839938 Functional Loss SNV dbSNP153 33..33 33 - - - 79401 RMVar_ID_79401 Human_SNP_ID_613991165 m1A Human chr16 + 89367463 89367463 89367463 AGACGCTCTCAAACGACCGGGAGTCTCAGGGGAGCGACGCTCTCAAACAACCCGGAGTGTACAGC AGACGCTCTCAAACGACCGGGAGTCTCAGGGGGGCGACGCTCTCAAACAACCCGGAGTGTACAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89367458..89367615;chr16:89367460..89367601 26863196 MeRIP-seq:(Medium) rs1335537826 Functional Loss SNV dbSNP153 33..33 33 - - - 79402 RMVar_ID_79402 Human_SNP_ID_613999757 m1A Human chr16 + 89393088 89393088 89393088 GGAGCCTCCGGCAAGCCCAGTCCCCAGGAAACACGGTCTCCCTCCCTCTTCTTCACCTGCATACC GGAGCCTCCGGCAAGCCCAGTCCCCAGGAAACCCGGTCTCCCTCCCTCTTCTTCACCTGCATACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89393086..89393154 26863196 MeRIP-seq:(Medium) rs1347342866 Functional Loss SNV dbSNP153 33..33 33 - - - 79403 RMVar_ID_79403 Human_SNP_ID_614002231 m1A Human chr16 - 89400795 89400795 89400795 CTCCAGCGCAGGGAAGCCTGGGGCAGCAGATGACCGGCCCCCAGCGCAGGGAAGCCTGGGGCAGC CTCCAGCGCAGGGAAGCCTGGGGCAGCAGATGTCCGGCCCCCAGCGCAGGGAAGCCTGGGGCAGC T A ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:89400788..89400903;chr16:89400791..89400924 26863196 MeRIP-seq:(Medium) rs1296729166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_325779,RMVar_hsa_circ_329884 79404 RMVar_ID_79404 Human_SNP_ID_614012425 m1A Human chr16 + 89431623 89431623 89431623 TTCTCTTGTGAACTTTGTTTCCATTTTGTTTCACTTGCTACATCTCCTTCCTCCACCTCCTCCCT TTCTCTTGTGAACTTTGTTTCCATTTTGTTTCCCTTGCTACATCTCCTTCCTCCACCTCCTCCCT A C AC092120.3 Ensembl:ENSG00000287351 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89431620..89431704 26863196 MeRIP-seq:(Medium) rs1013718464 Functional Loss SNV dbSNP153 33..33 33 - - - 79405 RMVar_ID_79405 Human_SNP_ID_614012491 m1A Human chr16 + 89431863 89431863 89431863 CACAGGCTGTGCACATACAGAGCCCTCACCCCACTCCTTCCTGTATCCCCTGCCTTGCTGCAGGG CACAGGCTGTGCACATACAGAGCCCTCACCCCGCTCCTTCCTGTATCCCCTGCCTTGCTGCAGGG A G AC092120.3 Ensembl:ENSG00000287351 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89431859..89432075 26863196 MeRIP-seq:(Medium) rs1033077452 Functional Loss SNV dbSNP153 33..33 33 - - - 79406 RMVar_ID_79406 Human_SNP_ID_614017955 m1A Human chr16 + 89447533 89447533 89447533 ATCCTACGAATCAGAGGGTCCTCGTGATCCCCATCCGTGCACTCACACTCCCTGCTGTGGTCCAC ATCCTACGAATCAGAGGGTCCTCGTGATCCCCGTCCGTGCACTCACACTCCCTGCTGTGGTCCAC A G AC092120.3 Ensembl:ENSG00000287351 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89447526..89447636 26863196 MeRIP-seq:(Medium) rs1448468507 Functional Loss SNV dbSNP153 33..33 33 - - - 79407 RMVar_ID_79407 Human_SNP_ID_614031733 m1A Human chr16 - 89488661 89488661 89488661 TATAAGATGATATTACCTGTGGAAAAAGTGCCATCGAAACAGTTACTGTTTTTGTTGTGTGCAGA TATAAGATGATATTACCTGTGGAAAAAGTGCCGTCGAAACAGTTACTGTTTTTGTTGTGTGCAGA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89488654..89488801 32194978 MeRIP-seq:(Medium) rs1354588515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855143 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 79408 RMVar_ID_79408 Human_SNP_ID_614032007 m1A Human chr16 + 89489260 89489260 89489260 CGCGCGCGCGCGCGCGCGCACACACATACACCACACACACAGCTACCGCCCTGCCAGGGGATGAT CGCGCGCGCGCGCGCGCGCACACACATACACCCCACACACAGCTACCGCCCTGCCAGGGGATGAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89489252..89489391 26863196 MeRIP-seq:(Medium) rs761585434 Functional Loss SNV dbSNP153 33..33 33 - - - 79409 RMVar_ID_79409 Human_SNP_ID_614032008 m1A Human chr16 + 89489260 89489260 89489260 CGCGCGCGCGCGCGCGCGCACACACATACACCACACACACAGCTACCGCCCTGCCAGGGGATGAT CGCGCGCGCGCGCGCGCGCACACACATACACCGCACACACAGCTACCGCCCTGCCAGGGGATGAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89489252..89489391 26863196 MeRIP-seq:(Medium) rs761585434 Functional Loss SNV dbSNP153 33..33 33 - - - 79410 RMVar_ID_79410 Human_SNP_ID_614032044 m1A Human chr16 + 89489324 89489324 89489324 TGAAATGAGGAACGGAAATTAACATTTCAGGCAACGTCTCACATTGTTCCTTGAGGCCAAGGGCT TGAAATGAGGAACGGAAATTAACATTTCAGGCCACGTCTCACATTGTTCCTTGAGGCCAAGGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89489319..89489577 26863196 MeRIP-seq:(Medium) rs901367445 Functional Loss SNV dbSNP153 33..33 33 - - - 79411 RMVar_ID_79411 Human_SNP_ID_614032538 m1A Human chr16 + 89490166 89490162 89490167 CGGAGGCCCGCGGCGCAGCTCCGTCGCCGGGGAAGGCCTGCAGGCCGCAAGGCCGCGCGAATGCC CGGAGGCCCGCGGCGCAGCTCCGTCGCCG_____GGCCTGCAGGCCGCAAGGCCGCGCGAATGCC GGGGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89490158..89490237 26863196 MeRIP-seq:(Medium) rs1318871840 Functional Loss DEL dbSNP153 30..34 33 - - - 79412 RMVar_ID_79412 Human_SNP_ID_614032691 m1A Human chr16 - 89490512 89490512 89490512 GGTGCGCGATGGACCGAGGGCCCCAGCCGGGGAGGCGCCGCCGCCGAGCCCGCGGCCAGACGCCC GGTGCGCGATGGACCGAGGGCCCCAGCCGGGGGGGCGCCGCCGCCGAGCCCGCGGCCAGACGCCC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:89489629..89490575;chr16:89490301..89490575;chr16:89490153..89490575;chr16:89490310..89490581 26863196 MeRIP-seq:(Medium) rs1322706636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503656,Human_RBP_ID_4390519,Human_RBP_ID_8086385,Human_RBP_ID_8442913,Human_RBP_ID_8726429,Human_RBP_ID_9286023,Human_RBP_ID_18418818,Human_RBP_ID_18484000,Human_RBP_ID_22944505,Human_RBP_ID_26329445,Human_RBP_ID_27838043 Human_miRNA_ID_2017972 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 79413 RMVar_ID_79413 Human_SNP_ID_614032699 m1A Human chr16 - 89490520 89490520 89490520 CCTGAGACGGTGCGCGATGGACCGAGGGCCCCAGCCGGGGAGGCGCCGCCGCCGAGCCCGCGGCC CCTGAGACGGTGCGCGATGGACCGAGGGCCCCGGCCGGGGAGGCGCCGCCGCCGAGCCCGCGGCC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr16:89490434..89490527;chr16:89490418..89490524 26863410 MeRIP-seq:(Medium) rs960872132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234009,Human_RBP_ID_3503656,Human_RBP_ID_4390520,Human_RBP_ID_8086385,Human_RBP_ID_8726429,Human_RBP_ID_9286023,Human_RBP_ID_9325590,Human_RBP_ID_18418818,Human_RBP_ID_18484000,Human_RBP_ID_22944505,Human_RBP_ID_26329445,Human_RBP_ID_27838043 Human_miRNA_ID_2685615 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 79414 RMVar_ID_79414 Human_SNP_ID_614032949 m1A Human chr16 - 89491007 89491007 89491007 CGGGGGCAGGCAGAAGACCACGGGCACGCGACAGGCAACCGCCGCCTCGGCTCTAGAGGTGGACG CGGGGGCAGGCAGAAGACCACGGGCACGCGACTGGCAACCGCCGCCTCGGCTCTAGAGGTGGACG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89490997..89491303 26863196 MeRIP-seq:(Medium) rs1414216195 Functional Loss SNV dbSNP153 33..33 33 - - - 79415 RMVar_ID_79415 Human_SNP_ID_614039243 m1A Human chr16 - 89508434 89508434 89508434 GGCCTGGACCCCGGCGGAGGGCACGGAGCAGCAGCAGCAGCACGGCCATGTTGGCCTGAAAGCCG GGCCTGGACCCCGGCGGAGGGCACGGAGCAGCTGCAGCAGCACGGCCATGTTGGCCTGAAAGCCG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89508401..89508625 26863196 MeRIP-seq:(Medium) rs1352999079 Functional Loss SNV dbSNP153 33..33 33 - - - 79416 RMVar_ID_79416 Human_SNP_ID_614039289 m1A Human chr16 - 89508484 89508484 89508484 GAACCCTGGACTCCAGGCCGGGCCTGGGCCCCACAGCGGCCGAGGACCCGGGCCTGGACCCCGGC GAACCCTGGACTCCAGGCCGGGCCTGGGCCCCGCAGCGGCCGAGGACCCGGGCCTGGACCCCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89508440..89508538 26863196 MeRIP-seq:(Medium) rs1419170613 Functional Loss SNV dbSNP153 33..33 33 - - - 79417 RMVar_ID_79417 Human_SNP_ID_614039290 m1A Human chr16 - 89508484 89508484 89508484 GAACCCTGGACTCCAGGCCGGGCCTGGGCCCCACAGCGGCCGAGGACCCGGGCCTGGACCCCGGC GAACCCTGGACTCCAGGCCGGGCCTGGGCCCCCCAGCGGCCGAGGACCCGGGCCTGGACCCCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89508440..89508538 26863196 MeRIP-seq:(Medium) rs1419170613 Functional Loss SNV dbSNP153 33..33 33 - - - 79418 RMVar_ID_79418 Human_SNP_ID_614043368 m1A Human chr16 - 89518821 89518821 89518821 GACACACGCGCAGTGTGTGCCCACCGCAGCTGAGGCAATCCAACCACAGGCTCCCTCCGGCTGTC GACACACGCGCAGTGTGTGCCCACCGCAGCTGGGGCAATCCAACCACAGGCTCCCTCCGGCTGTC T C lnc-ANKRD11-3,lnc-ANKRD11-3:2 RNACentral:URS00008BA1CB,RNACentral:URS00009C0173 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89518814..89518891 26863196 MeRIP-seq:(Medium) rs887286397 Functional Loss SNV dbSNP153 33..33 33 - - - 79419 RMVar_ID_79419 Human_SNP_ID_614048240 m1A Human chr16 + 89531863 89531863 89531863 GAGACCTTACCTCTAAAAAACAAAAAAACGGAATCCCCAAGTAGTTAGTGTTGCATTGTCTGCTG GAGACCTTACCTCTAAAAAACAAAAAAACGGAGTCCCCAAGTAGTTAGTGTTGCATTGTCTGCTG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89531860..89531977 26863196 MeRIP-seq:(Medium) rs773461773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_112642,RMVar_hsa_circ_180622,RMVar_hsa_circ_107505,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_110909,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_180626,RMVar_hsa_circ_296960,RMVar_hsa_circ_180628,RMVar_hsa_circ_87651,RMVar_hsa_circ_330094,RMVar_hsa_circ_180627,RMVar_hsa_circ_306711 79420 RMVar_ID_79420 Human_SNP_ID_614048573 m1A Human chr16 + 89532529 89532529 89532529 GGAAGCCCGAGCCCGGGCCCCCTGCATCGTCTACATCGATGAGATCGACGCGGTGGGCAAGAAGC GGAAGCCCGAGCCCGGGCCCCCTGCATCGTCTGCATCGATGAGATCGACGCGGTGGGCAAGAAGC A G SPG7 Ensembl:ENSG00000197912 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89531899..89532645 32194978 MeRIP-seq:(Medium) rs1319276066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22944510,Human_RBP_ID_27812085 Human_Splice_Rec_1751164,Human_Splice_Rec_1751200,Human_Splice_Rec_1751232,Human_Splice_Rec_1751262,Human_Splice_Rec_1751288,Human_Splice_Rec_1751350,Human_Splice_Rec_1751382,Human_Splice_Rec_1751420,Human_Splice_Rec_1751456,Human_Splice_Rec_1751490,Human_Splice_Rec_1751522,Human_Splice_Rec_1751580,Human_Splice_Rec_1751614,Human_Splice_Rec_1751646,Human_Splice_Rec_1751676,Human_Splice_Rec_1751708,Human_Splice_Rec_1751756,Human_Splice_Rec_1751786,Human_Splice_Rec_1751824,Human_Splice_Rec_1751858,Human_Splice_Rec_1751884,Human_Splice_Rec_1751930,Human_Splice_Rec_1751946,Human_Splice_Rec_1751966,Human_Splice_Rec_1751982,Human_Splice_Rec_1752014,Human_Splice_Rec_1752056,Human_Splice_Rec_1752090,Human_Splice_Rec_1752150,Human_Splice_Rec_1752164,Human_Splice_Rec_1752196,Human_Splice_Rec_1752230,Human_Splice_Rec_1752264,Human_Splice_Rec_1752276,Human_Splice_Rec_1752302,Human_Splice_Rec_1752328,Human_Splice_Rec_1752350,Human_Splice_Rec_1752362,Human_Splice_Rec_1752372,Human_Splice_Rec_1752400,Human_Splice_Rec_1752406,Human_Splice_Rec_1752424,Human_Splice_Rec_1752440,Human_Splice_Rec_1752448 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_112642,RMVar_hsa_circ_180622,RMVar_hsa_circ_107505,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_89397,RMVar_hsa_circ_39348,RMVar_hsa_circ_110909,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_180626,RMVar_hsa_circ_296960,RMVar_hsa_circ_330094,RMVar_hsa_circ_180627,RMVar_hsa_circ_306711,RMVar_hsa_circ_292292,RMVar_hsa_circ_98771,RMVar_hsa_circ_180631,RMVar_hsa_circ_93099,RMVar_hsa_circ_180632,RMVar_hsa_circ_180633,RMVar_hsa_circ_180634 79421 RMVar_ID_79421 Human_SNP_ID_614048574 m1A Human chr16 + 89532529 89532529 89532529 GGAAGCCCGAGCCCGGGCCCCCTGCATCGTCTACATCGATGAGATCGACGCGGTGGGCAAGAAGC GGAAGCCCGAGCCCGGGCCCCCTGCATCGTCTTCATCGATGAGATCGACGCGGTGGGCAAGAAGC A T SPG7 Ensembl:ENSG00000197912 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89531899..89532645 32194978 MeRIP-seq:(Medium) rs1319276066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22944510,Human_RBP_ID_27812085 Human_Splice_Rec_1751164,Human_Splice_Rec_1751200,Human_Splice_Rec_1751232,Human_Splice_Rec_1751262,Human_Splice_Rec_1751288,Human_Splice_Rec_1751350,Human_Splice_Rec_1751382,Human_Splice_Rec_1751420,Human_Splice_Rec_1751456,Human_Splice_Rec_1751490,Human_Splice_Rec_1751522,Human_Splice_Rec_1751580,Human_Splice_Rec_1751614,Human_Splice_Rec_1751646,Human_Splice_Rec_1751676,Human_Splice_Rec_1751708,Human_Splice_Rec_1751756,Human_Splice_Rec_1751786,Human_Splice_Rec_1751824,Human_Splice_Rec_1751858,Human_Splice_Rec_1751884,Human_Splice_Rec_1751930,Human_Splice_Rec_1751946,Human_Splice_Rec_1751966,Human_Splice_Rec_1751982,Human_Splice_Rec_1752014,Human_Splice_Rec_1752056,Human_Splice_Rec_1752090,Human_Splice_Rec_1752150,Human_Splice_Rec_1752164,Human_Splice_Rec_1752196,Human_Splice_Rec_1752230,Human_Splice_Rec_1752264,Human_Splice_Rec_1752276,Human_Splice_Rec_1752302,Human_Splice_Rec_1752328,Human_Splice_Rec_1752350,Human_Splice_Rec_1752362,Human_Splice_Rec_1752372,Human_Splice_Rec_1752400,Human_Splice_Rec_1752406,Human_Splice_Rec_1752424,Human_Splice_Rec_1752440,Human_Splice_Rec_1752448 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_112642,RMVar_hsa_circ_180622,RMVar_hsa_circ_107505,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_89397,RMVar_hsa_circ_39348,RMVar_hsa_circ_110909,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_180626,RMVar_hsa_circ_296960,RMVar_hsa_circ_330094,RMVar_hsa_circ_180627,RMVar_hsa_circ_306711,RMVar_hsa_circ_292292,RMVar_hsa_circ_98771,RMVar_hsa_circ_180631,RMVar_hsa_circ_93099,RMVar_hsa_circ_180632,RMVar_hsa_circ_180633,RMVar_hsa_circ_180634 79422 RMVar_ID_79422 Human_SNP_ID_614050460 m1A Human chr16 + 89537173 89537173 89537173 AGGCTTTGTTGCTTCCGTTCATGGAAGCGCACAGGATAGGGCCGACGCTGTGCCGGTCGTGGGGA AGGCTTTGTTGCTTCCGTTCATGGAAGCGCACGGGATAGGGCCGACGCTGTGCCGGTCGTGGGGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89537163..89537263 32194978 MeRIP-seq:(Medium) rs1394895268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_112642,RMVar_hsa_circ_180622,RMVar_hsa_circ_107505,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_89397,RMVar_hsa_circ_39348,RMVar_hsa_circ_110909,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_180627,RMVar_hsa_circ_306711,RMVar_hsa_circ_98771,RMVar_hsa_circ_93099,RMVar_hsa_circ_180632,RMVar_hsa_circ_180633,RMVar_hsa_circ_180634 79423 RMVar_ID_79423 Human_SNP_ID_614050543 m1A Human chr16 - 89537370 89537370 89537370 CCGCGTGTGGTCAGCGCCGACGCTCCCCATCAACGCTTTCCAGCACAGGAGCCGGGACCTGGACG CCGCGTGTGGTCAGCGCCGACGCTCCCCATCAGCGCTTTCCAGCACAGGAGCCGGGACCTGGACG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89537362..89537463 32194978 MeRIP-seq:(Medium) rs1479016060 Functional Loss SNV dbSNP153 33..33 33 - - - 79424 RMVar_ID_79424 Human_SNP_ID_614053308 m1A Human chr16 + 89544738 89544738 89544738 GGACGGTGCTCTGATGAGGCCAGGCCGACTGGACCGGCACGTCTTCATTGATCTCCCCACGCTGC GGACGGTGCTCTGATGAGGCCAGGCCGACTGGGCCGGCACGTCTTCATTGATCTCCCCACGCTGC A G SPG7 Ensembl:ENSG00000197912 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89544687..89545936 32194978 MeRIP-seq:(Medium) rs777935431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5572221,Human_RBP_ID_9373419,Human_RBP_ID_18987283,Human_RBP_ID_19075559,Human_RBP_ID_22944742 Human_Splice_Rec_1751166,Human_Splice_Rec_1751167,Human_Splice_Rec_1751202,Human_Splice_Rec_1751203,Human_Splice_Rec_1751234,Human_Splice_Rec_1751235,Human_Splice_Rec_1751294,Human_Splice_Rec_1751295,Human_Splice_Rec_1751352,Human_Splice_Rec_1751353,Human_Splice_Rec_1751384,Human_Splice_Rec_1751385,Human_Splice_Rec_1751426,Human_Splice_Rec_1751427,Human_Splice_Rec_1751458,Human_Splice_Rec_1751459,Human_Splice_Rec_1751492,Human_Splice_Rec_1751493,Human_Splice_Rec_1751524,Human_Splice_Rec_1751525,Human_Splice_Rec_1751584,Human_Splice_Rec_1751585,Human_Splice_Rec_1751616,Human_Splice_Rec_1751617,Human_Splice_Rec_1751649,Human_Splice_Rec_1751678,Human_Splice_Rec_1751679,Human_Splice_Rec_1751710,Human_Splice_Rec_1751711,Human_Splice_Rec_1751758,Human_Splice_Rec_1751759,Human_Splice_Rec_1751788,Human_Splice_Rec_1751794,Human_Splice_Rec_1751795,Human_Splice_Rec_1751826,Human_Splice_Rec_1751827,Human_Splice_Rec_1751860,Human_Splice_Rec_1751861,Human_Splice_Rec_1751886,Human_Splice_Rec_1751887,Human_Splice_Rec_1751948,Human_Splice_Rec_1751949,Human_Splice_Rec_1751984,Human_Splice_Rec_1751985,Human_Splice_Rec_1752016,Human_Splice_Rec_1752017,Human_Splice_Rec_1752060,Human_Splice_Rec_1752061,Human_Splice_Rec_1752122,Human_Splice_Rec_1752123,Human_Splice_Rec_1752170,Human_Splice_Rec_1752171,Human_Splice_Rec_1752202,Human_Splice_Rec_1752203,Human_Splice_Rec_1752232,Human_Splice_Rec_1752233,Human_Splice_Rec_1752266,Human_Splice_Rec_1752278,Human_Splice_Rec_1752279,Human_Splice_Rec_1752304,Human_Splice_Rec_1752305,Human_Splice_Rec_1752330,Human_Splice_Rec_1752331,Human_Splice_Rec_1752352,Human_Splice_Rec_1752353,Human_Splice_Rec_1752364,Human_Splice_Rec_1752365,Human_Splice_Rec_1752378,Human_Splice_Rec_1752379,Human_Splice_Rec_1752402,Human_Splice_Rec_1752403,Human_Splice_Rec_1752408,Human_Splice_Rec_1752409,Human_Splice_Rec_1752426,Human_Splice_Rec_1752427,Human_Splice_Rec_1752444,Human_Splice_Rec_1752445,Human_Splice_Rec_1752454,Human_Splice_Rec_1752456,Human_Splice_Rec_1752457,Human_Splice_Rec_1752466,Human_Splice_Rec_1752467,Human_Splice_Rec_1752484,Human_Splice_Rec_1752485,Human_Splice_Rec_1752490,Human_Splice_Rec_1752491,Human_Splice_Rec_1752506,Human_Splice_Rec_1752507,Human_Splice_Rec_1752512,Human_Splice_Rec_1752513,Human_Splice_Rec_1752531,Human_Splice_Rec_1752545,Human_Splice_Rec_1752549,Human_Splice_Rec_1752565,Human_Splice_Rec_1752581,Human_Splice_Rec_1752595,Human_Splice_Rec_1752611,Human_Splice_Rec_1752629,Human_Splice_Rec_1752643,Human_Splice_Rec_1752657,Human_Splice_Rec_1752673,Human_Splice_Rec_1752685,Human_Splice_Rec_1752703 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_112642,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_89397,RMVar_hsa_circ_39348,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_105016,RMVar_hsa_circ_79128,RMVar_hsa_circ_180633,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_180636,RMVar_hsa_circ_348324,RMVar_hsa_circ_273035,RMVar_hsa_circ_180638,RMVar_hsa_circ_180639,RMVar_hsa_circ_180637 79425 RMVar_ID_79425 Human_SNP_ID_614056719 m1A Human chr16 - 89553928 89553928 89553928 ATGGTCCATCATCTGCTGCAGGCCTTGGCTGAAGGGGCGCCGCCCGATGCCCATGAGGCCCTCCT ATGGTCCATCATCTGCTGCAGGCCTTGGCTGAGGGGGCGCCGCCCGATGCCCATGAGGCCCTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89553785..89553936 32194978 MeRIP-seq:(Medium) rs1567934405 Functional Loss SNV dbSNP153 33..33 33 - - - 79426 RMVar_ID_79426 Human_SNP_ID_614057826 m1A Human chr16 + 89557017 89557016 89557018 GCAGAGGTGGATCGACGCCCAGAGGGAGAAACAGGACTTGGGCGAGGAGGAGACCGAAGAGACCC GCAGAGGTGGATCGACGCCCAGAGGGAGAAAC__GACTTGGGCGAGGAGGAGACCGAAGAGACCC CAG C SPG7 Ensembl:ENSG00000197912 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89556926..89557117 26863196 MeRIP-seq:(Medium) rs774035870 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6129,Human_RBP_ID_481902,Human_RBP_ID_890864,Human_RBP_ID_9373424,Human_RBP_ID_18163649,Human_RBP_ID_18984501 RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_103409,RMVar_hsa_circ_123827,RMVar_hsa_circ_180643,RMVar_hsa_circ_180645,RMVar_hsa_circ_180646,RMVar_hsa_circ_120233 79427 RMVar_ID_79427 Human_SNP_ID_614057977 m1A Human chr16 + 89557434 89557434 89557434 CACCCAGAGGCAGCAGAGCATTCAGACTCCAAACAGACCCCTGTTCATGCCGACGCTTGCACGAC CACCCAGAGGCAGCAGAGCATTCAGACTCCAAGCAGACCCCTGTTCATGCCGACGCTTGCACGAC A G SPG7 Ensembl:ENSG00000197912 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89557384..89557565 26863196 MeRIP-seq:(Medium) rs772338990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481911,Human_RBP_ID_18687608 RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_103409,RMVar_hsa_circ_123827,RMVar_hsa_circ_180643,RMVar_hsa_circ_180645,RMVar_hsa_circ_180646,RMVar_hsa_circ_120233 79428 RMVar_ID_79428 Human_SNP_ID_614059511 m1A Human chr16 + 89560991 89560991 89560991 CATGGCGCCCAGCCGGAATGGCATGGTCTTGAAGCCCCACTTCCACAAGGACTGGCAGCGGCGCG CATGGCGCCCAGCCGGAATGGCATGGTCTTGATGCCCCACTTCCACAAGGACTGGCAGCGGCGCG A T RPL13 Ensembl:ENSG00000167526 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89560741..89561000 26863196 MeRIP-seq:(Medium) rs1375818051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481923,Human_RBP_ID_4394112,Human_RBP_ID_5142111,Human_RBP_ID_17653145,Human_RBP_ID_18190295,Human_RBP_ID_18687622 Human_Splice_Rec_1752792,Human_Splice_Rec_1752793,Human_Splice_Rec_1752802,Human_Splice_Rec_1752808,Human_Splice_Rec_1752809,Human_Splice_Rec_1752824,Human_Splice_Rec_1752825,Human_Splice_Rec_1752834,Human_Splice_Rec_1752836,Human_Splice_Rec_1752837,Human_Splice_Rec_1752844,Human_Splice_Rec_1752845,Human_Splice_Rec_1752850,Human_Splice_Rec_1752851,Human_Splice_Rec_1752861,Human_Splice_Rec_1752865 RMVar_hsa_circ_22467,RMVar_hsa_circ_41998 79429 RMVar_ID_79429 Human_SNP_ID_614059547 m1A Human chr16 - 89561052 89561052 89561052 AGCCCCGAGCGCAGGGCTCACCTGCGGATCTTACGGGCCGGCTGGTTGAACCACGTGGCCACGCG AGCCCCGAGCGCAGGGCTCACCTGCGGATCTTCCGGGCCGGCTGGTTGAACCACGTGGCCACGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89561001..89561075 32194978 MeRIP-seq:(Medium) rs2280370 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 79430 RMVar_ID_79430 Human_SNP_ID_614059550 m1A Human chr16 + 89561062 89561062 89561062 CGTGGTTCAACCAGCCGGCCCGTAAGATCCGCAGGTGAGCCCTGCGCTCGGGGCTGCCCCTGGGG CGTGGTTCAACCAGCCGGCCCGTAAGATCCGCCGGTGAGCCCTGCGCTCGGGGCTGCCCCTGGGG A C RPL13 Ensembl:ENSG00000167526 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs780661827 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_481925,Human_RBP_ID_4390696,Human_RBP_ID_8442991,Human_RBP_ID_8811289,Human_RBP_ID_18190299,Human_RBP_ID_19075566,Human_RBP_ID_26810749 Human_Splice_Rec_1752793,Human_Splice_Rec_1752809,Human_Splice_Rec_1752825,Human_Splice_Rec_1752837,Human_Splice_Rec_1752845,Human_Splice_Rec_1752851,Human_Splice_Rec_1752861,Human_Splice_Rec_1752865 RMVar_hsa_circ_22467,RMVar_hsa_circ_41998 79431 RMVar_ID_79431 Human_SNP_ID_614059688 m1A Human chr16 - 89561259 89561259 89561259 GCCGGATGGGACCCGACGCGGGGCGCGGGGCGATGCGGCGCGCCTTGGCTTGCCGGGCCTTACGT GCCGGATGGGACCCGACGCGGGGCGCGGGGCGTTGCGGCGCGCCTTGGCTTGCCGGGCCTTACGT T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89561010..89561413 26863196 MeRIP-seq:(Medium) rs1194720855 Functional Loss SNV dbSNP153 33..33 33 - - - 79432 RMVar_ID_79432 Human_SNP_ID_614059711 m1A Human chr16 - 89561281 89561281 89561281 ACCGTGGGGCAGCGCACGATGGGCCGGATGGGACCCGACGCGGGGCGCGGGGCGATGCGGCGCGC ACCGTGGGGCAGCGCACGATGGGCCGGATGGGCCCCGACGCGGGGCGCGGGGCGATGCGGCGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr16:89561225..89561397;chr16:89561176..89561421;chr16:89561180..89561433;chr16:89561175..89561404;chr16:89560651..89561425;chr16:89561189..89561397;chr16:89561226..89561375 26863196,26863410,26863196,32194978 MeRIP-seq:(Medium) rs564290531 Functional Loss SNV dbSNP153 33..33 33 - - - 79433 RMVar_ID_79433 Human_SNP_ID_614059869 m1A Human chr16 + 89561536 89561536 89561536 TGAGGCTTTTCATCCAGGCCTCGGGGCTGGAGAAAGCCCGGGCCTGTCTCCATCTCTCTCTGGTT TGAGGCTTTTCATCCAGGCCTCGGGGCTGGAGCAAGCCCGGGCCTGTCTCCATCTCTCTCTGGTT A C RPL13 Ensembl:ENSG00000167526 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:89561532..89561802 26863410 MeRIP-seq:(Medium) rs748950826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274868,Human_RBP_ID_8252363,Human_RBP_ID_22053650,Human_RBP_ID_22541975,Human_RBP_ID_22653386,Human_RBP_ID_23256806 Human_Splice_Rec_1752855 RMVar_hsa_circ_100471,RMVar_hsa_circ_41998,RMVar_hsa_circ_180648 79434 RMVar_ID_79434 Human_SNP_ID_614059959 m1A Human chr16 + 89561669 89561669 89561669 GCGGAACAAGTCCACGGAGTCCCTGCAGGCCAACGTGCAGCGGCTGAAGGAGTACCGCTCCAAAC GCGGAACAAGTCCACGGAGTCCCTGCAGGCCAGCGTGCAGCGGCTGAAGGAGTACCGCTCCAAAC A G RPL13 Ensembl:ENSG00000167526 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr16:89561535..89561714;chr16:89561576..89561725 26863196,32194978 MeRIP-seq:(Medium) rs1477572257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234013,Human_RBP_ID_481941,Human_RBP_ID_1005949,Human_RBP_ID_1525853,Human_RBP_ID_1847992,Human_RBP_ID_4390715,Human_RBP_ID_8443000,Human_RBP_ID_9066523,Human_RBP_ID_9326368,Human_RBP_ID_17255692,Human_RBP_ID_17488057,Human_RBP_ID_17691042,Human_RBP_ID_17882901,Human_RBP_ID_18190305,Human_RBP_ID_18687635,Human_RBP_ID_22053652,Human_RBP_ID_22442287,Human_RBP_ID_22498604,Human_RBP_ID_22532876,Human_RBP_ID_22802677,Human_RBP_ID_26444401,Human_RBP_ID_26810765,Human_RBP_ID_26952912,Human_RBP_ID_27248733 Human_Splice_Rec_1752796,Human_Splice_Rec_1752797,Human_Splice_Rec_1752804,Human_Splice_Rec_1752805,Human_Splice_Rec_1752811,Human_Splice_Rec_1752818,Human_Splice_Rec_1752819,Human_Splice_Rec_1752828,Human_Splice_Rec_1752829,Human_Splice_Rec_1752838,Human_Splice_Rec_1752839,Human_Splice_Rec_1752848,Human_Splice_Rec_1752854,Human_Splice_Rec_1752857,Human_Splice_Rec_1752864,Human_Splice_Rec_1752868,Human_Splice_Rec_1752869,Human_Splice_Rec_1752874,Human_Splice_Rec_1752875 RMVar_hsa_circ_100471,RMVar_hsa_circ_41998,RMVar_hsa_circ_180648,RMVar_hsa_circ_98439,RMVar_hsa_circ_180650 79435 RMVar_ID_79435 Human_SNP_ID_614059961 m1A Human chr16 + 89561683 89561683 89561683 CGGAGTCCCTGCAGGCCAACGTGCAGCGGCTGAAGGAGTACCGCTCCAAACTCATCCTCTTCCCC CGGAGTCCCTGCAGGCCAACGTGCAGCGGCTGGAGGAGTACCGCTCCAAACTCATCCTCTTCCCC A G RPL13 Ensembl:ENSG00000167526 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89561534..89561732 26863196 MeRIP-seq:(Medium) rs758084824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481941,Human_RBP_ID_1525853,Human_RBP_ID_8443000,Human_RBP_ID_9066524,Human_RBP_ID_9326368,Human_RBP_ID_18190305,Human_RBP_ID_22054369,Human_RBP_ID_26810766 Human_Splice_Rec_1752797,Human_Splice_Rec_1752805,Human_Splice_Rec_1752811,Human_Splice_Rec_1752819,Human_Splice_Rec_1752829,Human_Splice_Rec_1752838,Human_Splice_Rec_1752839,Human_Splice_Rec_1752857,Human_Splice_Rec_1752869,Human_Splice_Rec_1752875 RMVar_hsa_circ_100471,RMVar_hsa_circ_41998,RMVar_hsa_circ_180648,RMVar_hsa_circ_98439,RMVar_hsa_circ_180650 79436 RMVar_ID_79436 Human_SNP_ID_614062955 m1A Human chr16 + 89568522 89568507 89568523 GCAGGGAGATGAAGGGAGGAAGGTATTTGTTCACGAGTTAGGGGCAGTTCACAAGATAAGAGCAA GCAGGGAGATGAAGGGAG________________GAGTTAGGGGCAGTTCACAAGATAAGAGCAA GGAAGGTATTTGTTCAC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89568431..89568549 26863196 MeRIP-seq:(Medium) rs1263822867 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_12856958 79437 RMVar_ID_79437 Human_SNP_ID_614063660 m1A Human chr16 - 89570675 89570675 89570675 CTGTGCCCAGGGACCACCTCCCCAGCCCGCAGACCACCTGTGCCCACTTGCCTCCTCCCAGGCTG CTGTGCCCAGGGACCACCTCCCCAGCCCGCAGTCCACCTGTGCCCACTTGCCTCCTCCCAGGCTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89570669..89570897 26863196 MeRIP-seq:(Medium) rs940199436 Functional Loss SNV dbSNP153 33..33 33 - - - 79438 RMVar_ID_79438 Human_SNP_ID_614064252 m1A Human chr16 - 89571953 89571953 89571953 AGGCGCGTTCTCGCGTGCAGCCCCGGGCCGCCATCCCTCCTGCCCCTTGTCTGCATGCAGCCAGG AGGCGCGTTCTCGCGTGCAGCCCCGGGCCGCCCTCCCTCCTGCCCCTTGTCTGCATGCAGCCAGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89571921..89572079 26863196 MeRIP-seq:(Medium) rs995193983 Functional Loss SNV dbSNP153 33..33 33 - - - 79439 RMVar_ID_79439 Human_SNP_ID_614067038 m1A Human chr16 - 89579493 89579470 89579494 GGGATGTTCTGTGTGATGGGATGTTCCGTGTGACGGGTGATCGGATGTTCCGTGTCAGCAGGTGA GGGATGTTCTGTGTGATGGGATGTTCCGTGT________________________CAGCAGGTGA GACACGGAACATCCGATCACCCGTC G lnc-CHMP1A-3 RNACentral:URS00009AF30F lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89579484..89579746 26863196 MeRIP-seq:(Medium) rs1318731371 Functional Loss DEL dbSNP153 32..55 33 - - - 79440 RMVar_ID_79440 Human_SNP_ID_614067817 m1A Human chr16 + 89581045 89581039 89581046 CATCCCGTCACCCGTCACACGGAACATCCCGTAACCCATCACATGGAACATCCCGTCACCTGTCA CATCCCGTCACCCGTCACACGGAACAT_______CCCATCACATGGAACATCCCGTCACCTGTCA TCCCGTAA T CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89581015..89581432 26863196 MeRIP-seq:(Medium) rs201229635 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_199004,Human_RBP_ID_261183,Human_RBP_ID_2490840,Human_RBP_ID_9420297,Human_RBP_ID_22370132,Human_RBP_ID_24531483,Human_RBP_ID_26810792 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 79441 RMVar_ID_79441 Human_SNP_ID_614067821 m1A Human chr16 + 89581045 89581045 89581045 CATCCCGTCACCCGTCACACGGAACATCCCGTAACCCATCACATGGAACATCCCGTCACCTGTCA CATCCCGTCACCCGTCACACGGAACATCCCGTCACCCATCACATGGAACATCCCGTCACCTGTCA A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89581015..89581432 26863196 MeRIP-seq:(Medium) rs1352083744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199004,Human_RBP_ID_261183,Human_RBP_ID_2490840,Human_RBP_ID_9420297,Human_RBP_ID_22370132,Human_RBP_ID_24531483,Human_RBP_ID_26810792 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 79442 RMVar_ID_79442 Human_SNP_ID_614068700 m1A Human chr16 + 89583518 89583518 89583518 GAGGTGGTGGACGTGCAGGGGTGGCCACACGCAGGGATGGCAGGTGCTTGAGAGCAGCCACAAAG GAGGTGGTGGACGTGCAGGGGTGGCCACACGCCGGGATGGCAGGTGCTTGAGAGCAGCCACAAAG A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89583508..89583601 26863196 MeRIP-seq:(Medium) rs200338413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2490859,Human_RBP_ID_9421210 Human_Splice_Rec_1752916,Human_Splice_Rec_1752917,Human_Splice_Rec_1752946,Human_Splice_Rec_1752947 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 79443 RMVar_ID_79443 Human_SNP_ID_614069623 m1A Human chr16 - 89585501 89585501 89585501 CGCAGCTGCAGAGGGAACTCAGAGAGACTTTGAAGGCCTCCCACACCGGGTTCAGGTTGTTCTTC CGCAGCTGCAGAGGGAACTCAGAGAGACTTTGGAGGCCTCCCACACCGGGTTCAGGTTGTTCTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89585465..89585580 26863196 MeRIP-seq:(Medium) rs375437368 Functional Loss SNV dbSNP153 33..33 33 - - - 79444 RMVar_ID_79444 Human_SNP_ID_614070465 m1A Human chr16 + 89587100 89587100 89587100 ACTATATCATGGGCGGCTGCCAGATCCACTTCACCGTGAGTCCATGGCCCCGCCCCATGCCGCCC ACTATATCATGGGCGGCTGCCAGATCCACTTCGCCGTGAGTCCATGGCCCCGCCCCATGCCGCCC A G CPNE7 Ensembl:ENSG00000178773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89587016..89587189;chr16:89586943..89587134 26863196 MeRIP-seq:(Medium) rs781079706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18411595,Human_RBP_ID_19077303,Human_RBP_ID_26329473,Human_RBP_ID_27838342 Human_Splice_Rec_1752898,Human_Splice_Rec_1752899,Human_Splice_Rec_1752930,Human_Splice_Rec_1752931,Human_Splice_Rec_1752956,Human_Splice_Rec_1752957,Human_Splice_Rec_1752959 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79445 RMVar_ID_79445 Human_SNP_ID_614071095 m1A Human chr16 - 89587661 89587658 89587661 CGTATCTATGGGTGACGCGGGGTCTGCGGGTGACATGGGGGTGACACGGGGTCTGTGCCGGGCTC CGTATCTATGGGTGACGCGGGGTCTGCGGGTG___TGGGGGTGACACGGGGTCTGTGCCGGGCTC ATGT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:89587610..89587755 26863196 MeRIP-seq:(Medium) rs1237933481 Functional Loss DEL dbSNP153 33..35 33 - - - 79446 RMVar_ID_79446 Human_SNP_ID_614071100 m1A Human chr16 - 89587661 89587661 89587661 CGTATCTATGGGTGACGCGGGGTCTGCGGGTGACATGGGGGTGACACGGGGTCTGTGCCGGGCTC CGTATCTATGGGTGACGCGGGGTCTGCGGGTGCCATGGGGGTGACACGGGGTCTGTGCCGGGCTC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:89587610..89587755 26863196 MeRIP-seq:(Medium) rs1451656488 Functional Loss SNV dbSNP153 33..33 33 - - - 79447 RMVar_ID_79447 Human_SNP_ID_614071110 m1A Human chr16 + 89587695 89587670 89587696 ACCCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGT ACCCGCAG__________________________ACCCCGTGTCACCCCCATAGCACCCCCGTGT GACCCCGCGTCACCCATAGATACGCAC G CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89587414..89587875 26863196 MeRIP-seq:(Medium) rs1423616966 Functional Loss DEL dbSNP153 9..34 33 - - - Human_RBP_ID_45606,Human_RBP_ID_2490865,Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79448 RMVar_ID_79448 Human_SNP_ID_614071127 m1A Human chr16 + 89587697 89587682 89587697 CCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGTCA CCGCAGACCCCGCGTCAC_______________CCCCGTGTCACCCCCATAGCACCCCCGTGTCA CCCATAGATACGCACA C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89587513..89587738 26863196 MeRIP-seq:(Medium) rs1309906085 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79449 RMVar_ID_79449 Human_SNP_ID_614071141 m1A Human chr16 + 89587695 89587695 89587695 ACCCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGT ACCCGCAGACCCCGCGTCACCCATAGATACGCCCACCCCGTGTCACCCCCATAGCACCCCCGTGT A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89587414..89587875 26863196 MeRIP-seq:(Medium) rs1484171897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45606,Human_RBP_ID_2490865,Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79450 RMVar_ID_79450 Human_SNP_ID_614071142 m1A Human chr16 + 89587695 89587695 89587695 ACCCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGT ACCCGCAGACCCCGCGTCACCCATAGATACGCGCACCCCGTGTCACCCCCATAGCACCCCCGTGT A G CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89587414..89587875 26863196 MeRIP-seq:(Medium) rs1484171897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45606,Human_RBP_ID_2490865,Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79451 RMVar_ID_79451 Human_SNP_ID_614071143 m1A Human chr16 + 89587697 89587696 89587697 CCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGTCA CCGCAGACCCCGCGTCACCCATAGATACGCAC_CCCCGTGTCACCCCCATAGCACCCCCGTGTCA CA C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89587513..89587738 26863196 MeRIP-seq:(Medium) rs1202942912 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79452 RMVar_ID_79452 Human_SNP_ID_614071149 m1A Human chr16 + 89587697 89587697 89587697 CCGCAGACCCCGCGTCACCCATAGATACGCACACCCCGTGTCACCCCCATAGCACCCCCGTGTCA CCGCAGACCCCGCGTCACCCATAGATACGCACCCCCCGTGTCACCCCCATAGCACCCCCGTGTCA A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89587513..89587738 26863196 MeRIP-seq:(Medium) rs1306621869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17078046 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180657,RMVar_hsa_circ_373172,RMVar_hsa_circ_180659,RMVar_hsa_circ_180658,RMVar_hsa_circ_375555 79453 RMVar_ID_79453 Human_SNP_ID_614071870 m1A Human chr16 - 89588253 89588250 89588254 TCGTTCAACAAAACACGAACCAGCGCATCTGCAAATAACACGCGGGTGACACGGGGGCCGTGTAT TCGTTCAACAAAACACGAACCAGCGCATCTG____TAACACGCGGGTGACACGGGGGCCGTGTAT ATTTG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89588201..89588831 26863196 MeRIP-seq:(Medium) rs1555624263 Functional Loss DEL dbSNP153 32..35 33 - - - 79454 RMVar_ID_79454 Human_SNP_ID_614071873 m1A Human chr16 - 89588253 89588253 89588253 TCGTTCAACAAAACACGAACCAGCGCATCTGCAAATAACACGCGGGTGACACGGGGGCCGTGTAT TCGTTCAACAAAACACGAACCAGCGCATCTGCGAATAACACGCGGGTGACACGGGGGCCGTGTAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89588201..89588831 26863196 MeRIP-seq:(Medium) rs1016873289 Functional Loss SNV dbSNP153 33..33 33 - - - 79455 RMVar_ID_79455 Human_SNP_ID_614072148 m1A Human chr16 - 89588701 89588701 89588701 TAGTGCAGGGAGCAGCTGTTCCGCGGGTCTCCATTGGAGGCGGTGAAGTCAATGGCCACCTGCAG TAGTGCAGGGAGCAGCTGTTCCGCGGGTCTCCTTTGGAGGCGGTGAAGTCAATGGCCACCTGCAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89588651..89588725 32194978 MeRIP-seq:(Medium) rs755253774 Functional Loss SNV dbSNP153 33..33 33 - - - 79456 RMVar_ID_79456 Human_SNP_ID_614072149 m1A Human chr16 - 89588701 89588701 89588701 TAGTGCAGGGAGCAGCTGTTCCGCGGGTCTCCATTGGAGGCGGTGAAGTCAATGGCCACCTGCAG TAGTGCAGGGAGCAGCTGTTCCGCGGGTCTCCGTTGGAGGCGGTGAAGTCAATGGCCACCTGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89588651..89588725 32194978 MeRIP-seq:(Medium) rs755253774 Functional Loss SNV dbSNP153 33..33 33 - - - 79457 RMVar_ID_79457 Human_SNP_ID_614073424 m1A Human chr16 - 89591226 89591226 89591226 AGGCTTTCCCGGTGCTCTCCTCGGCCGCCGCCACGCGTGCCACCTTGGAGATGATGGGCGCCACG AGGCTTTCCCGGTGCTCTCCTCGGCCGCCGCCCCGCGTGCCACCTTGGAGATGATGGGCGCCACG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89591180..89591469 26863196 MeRIP-seq:(Medium) rs1464731596 Functional Loss SNV dbSNP153 33..33 33 - - - 79458 RMVar_ID_79458 Human_SNP_ID_614075398 m1A Human chr16 + 89595485 89595485 89595485 GCCCATGTCCATCATCATCGTGGGCGTGGGCAACGCCGACTTCACCGACATGCAGGTCCTGGACG GCCCATGTCCATCATCATCGTGGGCGTGGGCAGCGCCGACTTCACCGACATGCAGGTCCTGGACG A G CPNE7 Ensembl:ENSG00000178773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89595436..89595637 26863196 MeRIP-seq:(Medium) rs1408111525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22053662 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655,RMVar_hsa_circ_106104,RMVar_hsa_circ_180658,RMVar_hsa_circ_100269,RMVar_hsa_circ_180660 79459 RMVar_ID_79459 Human_SNP_ID_614075635 m1A Human chr16 - 89595894 89595894 89595894 ACGTGTGTGCTGTGCGTGTCTCGCCGGGTCGCAGAGGTTGGCAGCAACGGGGGAAGCCGCGTGGT ACGTGTGTGCTGTGCGTGTCTCGCCGGGTCGCGGAGGTTGGCAGCAACGGGGGAAGCCGCGTGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89595770..89596028 26863196 MeRIP-seq:(Medium) rs1364045013 Functional Loss SNV dbSNP153 33..33 33 - - - 79460 RMVar_ID_79460 Human_SNP_ID_614076005 m1A Human chr16 + 89596601 89596601 89596601 CGAGAAGCCTGGGTGTCCCTGCCGGAGAGGCCAGCCCAGGCTGCACACCGTGAAGATGTGGAGGG CGAGAAGCCTGGGTGTCCCTGCCGGAGAGGCCCGCCCAGGCTGCACACCGTGAAGATGTGGAGGG A C CPNE7 Ensembl:ENSG00000178773 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89596550..89596677 26863196 MeRIP-seq:(Medium) rs1405979452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100269,RMVar_hsa_circ_180660 79461 RMVar_ID_79461 Human_SNP_ID_614076006 m1A Human chr16 + 89596601 89596601 89596601 CGAGAAGCCTGGGTGTCCCTGCCGGAGAGGCCAGCCCAGGCTGCACACCGTGAAGATGTGGAGGG CGAGAAGCCTGGGTGTCCCTGCCGGAGAGGCCGGCCCAGGCTGCACACCGTGAAGATGTGGAGGG A G CPNE7 Ensembl:ENSG00000178773 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89596550..89596677 26863196 MeRIP-seq:(Medium) rs1405979452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100269,RMVar_hsa_circ_180660 79462 RMVar_ID_79462 Human_SNP_ID_614096221 m1A Human chr16 - 89645195 89645192 89645195 AGGACCTTTCCTTGGGGCCCTGCTTCATGACGATGCTGCCTGTGTCACCCTCTACCATCTGTAAA AGGACCTTTCCTTGGGGCCCTGCTTCATGACG___CTGCCTGTGTCACCCTCTACCATCTGTAAA GCAT G CHMP1A Ensembl:ENSG00000131165 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89644479..89645400 32194978 MeRIP-seq:(Medium) rs1380278538 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_26810801,Human_RBP_ID_27447514 Human_miRNA_ID_41708,Human_miRNA_ID_70426,Human_miRNA_ID_1938159,Human_miRNA_ID_1949259 RMVar_hsa_circ_96488,RMVar_hsa_circ_126095,RMVar_hsa_circ_106784,RMVar_hsa_circ_180663,RMVar_hsa_circ_180665,RMVar_hsa_circ_77309,RMVar_hsa_circ_180664,RMVar_hsa_circ_180662 79463 RMVar_ID_79463 Human_SNP_ID_614096302 m1A Human chr16 - 89645432 89645432 89645432 CACTTCCCTCAGTTCCCAAAGCTGCCCAGTCCATGGGGACAGAACCGTCACTCAGATCCACATTC CACTTCCCTCAGTTCCCAAAGCTGCCCAGTCCGTGGGGACAGAACCGTCACTCAGATCCACATTC T C CHMP1A Ensembl:ENSG00000131165 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89645381..89645492 26863196 MeRIP-seq:(Medium) rs1237340788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482063,Human_RBP_ID_1005972,Human_RBP_ID_1848010,Human_RBP_ID_12857207,Human_RBP_ID_17488335,Human_RBP_ID_26445537,Human_RBP_ID_27447518 Human_miRNA_ID_130084,Human_miRNA_ID_1981151,Human_miRNA_ID_1982875 RMVar_hsa_circ_96488,RMVar_hsa_circ_126095,RMVar_hsa_circ_106784,RMVar_hsa_circ_180663,RMVar_hsa_circ_180665,RMVar_hsa_circ_77309,RMVar_hsa_circ_180664,RMVar_hsa_circ_180662 79464 RMVar_ID_79464 Human_SNP_ID_614098098 m1A Human chr16 - 89649439 89649439 89649439 TGCCCGTGTGTATGCCGAGAACGCCATCCGCAAGAAGAACGAAGGTGTGAACTGGCTTCGGATGG TGCCCGTGTGTATGCCGAGAACGCCATCCGCAGGAAGAACGAAGGTGTGAACTGGCTTCGGATGG T C CHMP1A Ensembl:ENSG00000131165 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89649388..89649516 26863196 MeRIP-seq:(Medium) rs201973308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12857253,Human_RBP_ID_18987309,Human_RBP_ID_23707628 Human_Splice_Rec_1753100,Human_Splice_Rec_1753101,Human_Splice_Rec_1753110,Human_Splice_Rec_1753111,Human_Splice_Rec_1753117,Human_Splice_Rec_1753128,Human_Splice_Rec_1753129,Human_Splice_Rec_1753140,Human_Splice_Rec_1753141,Human_Splice_Rec_1753152,Human_Splice_Rec_1753153,Human_Splice_Rec_1753155,Human_Splice_Rec_1753160,Human_Splice_Rec_1753161,Human_Splice_Rec_1753168 RMVar_hsa_circ_75944,RMVar_hsa_circ_126095,RMVar_hsa_circ_180665,RMVar_hsa_circ_77309,RMVar_hsa_circ_180664,RMVar_hsa_circ_106777,RMVar_hsa_circ_180666,RMVar_hsa_circ_180667 79465 RMVar_ID_79465 Human_SNP_ID_614098118 m1A Human chr16 + 89649471 89649471 89649471 TTGCGGATGGCGTTCTCGGCATACACACGGGCACACTCTACATTTTTCTGCAGAAGGGCCTGAAA TTGCGGATGGCGTTCTCGGCATACACACGGGCGCACTCTACATTTTTCTGCAGAAGGGCCTGAAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89649362..89657598 32194978 MeRIP-seq:(Medium) rs774107724 Functional Loss SNV dbSNP153 33..33 33 - - - 79466 RMVar_ID_79466 Human_SNP_ID_614100189 m1A Human chr16 + 89655348 89655348 89655348 CGTCCCACCCAACTCACTGTGGGATGCTGGCCAAACCGCCCTCCTCATCTCAGCTTTCCCTCACC CGTCCCACCCAACTCACTGTGGGATGCTGGCCCAACCGCCCTCCTCATCTCAGCTTTCCCTCACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89655343..89655503 26863196 MeRIP-seq:(Medium) rs1392403908 Functional Loss SNV dbSNP153 33..33 33 - - - 79467 RMVar_ID_79467 Human_SNP_ID_614100221 m1A Human chr16 - 89655402 89655402 89655402 AGCTGAGGTGAGGGAAAGCTGAGGTGAGGGAAAGCTGAGGTGAGGGAAAGCTGAGGTGAGGGAAA AGCTGAGGTGAGGGAAAGCTGAGGTGAGGGAAGGCTGAGGTGAGGGAAAGCTGAGGTGAGGGAAA T C CHMP1A Ensembl:ENSG00000131165 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89655400..89655491 26863196 MeRIP-seq:(Medium) rs1434895274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126095,RMVar_hsa_circ_180665 79468 RMVar_ID_79468 Human_SNP_ID_614101169 m1A Human chr16 - 89657637 89657637 89657637 TTCGATCGCCGCCGGGACCTGACACCGCCCGGAGTTGGCGTCCCTTCTCCCTCTCCGAGTGCTGC TTCGATCGCCGCCGGGACCTGACACCGCCCGGGGTTGGCGTCCCTTCTCCCTCTCCGAGTGCTGC T C CHMP1A Ensembl:ENSG00000131165 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89657576..89657675 26863196 MeRIP-seq:(Medium) rs745501139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233628,Human_RBP_ID_4390860,Human_RBP_ID_9373428 Human_Splice_Rec_1753095,Human_Splice_Rec_1753107,Human_Splice_Rec_1753123,Human_Splice_Rec_1753135,Human_Splice_Rec_1753147,Human_Splice_Rec_1753157,Human_Splice_Rec_1753163 RMVar_hsa_circ_126095,RMVar_hsa_circ_180665 79469 RMVar_ID_79469 Human_SNP_ID_614101627 m1A Human chr16 + 89658263 89658263 89658263 TGATCCATATATTTCAGGTGAGGAGCAAAAGAAGGGATCCACCTATTCAGTTCCAAAATCTAAGG TGATCCATATATTTCAGGTGAGGAGCAAAAGACGGGATCCACCTATTCAGTTCCAAAATCTAAGG A C SPATA33 Ensembl:ENSG00000167523 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89658245..89658512 26863196 MeRIP-seq:(Medium) rs750928089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199911,Human_RBP_ID_9373430,Human_RBP_ID_22542649 Human_Splice_Rec_1753170,Human_Splice_Rec_1753174,Human_Splice_Rec_1753178,Human_Splice_Rec_1753184,Human_Splice_Rec_1753188,Human_Splice_Rec_1753192 79470 RMVar_ID_79470 Human_SNP_ID_614106033 m1A Human chr16 - 89669769 89669769 89669769 GTGCACCCTCCCCGAGAGCACTGGAGAAGGGGACTGCAGTTTCTCACGGCGGGGGCAGGCCTGGT GTGCACCCTCCCCGAGAGCACTGGAGAAGGGGGCTGCAGTTTCTCACGGCGGGGGCAGGCCTGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89669722..89669973 32194978 MeRIP-seq:(Medium) rs604868 Functional Loss SNV dbSNP153 33..33 33 - - - 79471 RMVar_ID_79471 Human_SNP_ID_614106034 m1A Human chr16 - 89669769 89669769 89669769 GTGCACCCTCCCCGAGAGCACTGGAGAAGGGGACTGCAGTTTCTCACGGCGGGGGCAGGCCTGGT GTGCACCCTCCCCGAGAGCACTGGAGAAGGGGCCTGCAGTTTCTCACGGCGGGGGCAGGCCTGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89669722..89669973 32194978 MeRIP-seq:(Medium) rs604868 Functional Loss SNV dbSNP153 33..33 33 - - - 79472 RMVar_ID_79472 Human_SNP_ID_614112813 m1A Human chr16 + 89686793 89686793 89686793 TAAGGAGGGCTTCTTCACGGTGCCTCCGGAACACAGGGTGCGCGGGGTGCCACCCGGGCAGCTCT TAAGGAGGGCTTCTTCACGGTGCCTCCGGAACCCAGGGTGCGCGGGGTGCCACCCGGGCAGCTCT A C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89686754..89687008 32194978 MeRIP-seq:(Medium) rs1179411371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235185,Human_RBP_ID_18411596,Human_RBP_ID_26779394 Human_Splice_Rec_1753271,Human_Splice_Rec_1753279,Human_Splice_Rec_1753303,Human_Splice_Rec_1753313,Human_Splice_Rec_1753335,Human_Splice_Rec_1753369,Human_Splice_Rec_1753371,Human_Splice_Rec_1753411 79473 RMVar_ID_79473 Human_SNP_ID_614113028 m1A Human chr16 - 89687181 89687181 89687181 CTCCATGCAGCCCAAGCCCAGCGGGAGCCTTCAAGCTCGAACTCGTCGCGGGTGTAAATTCTCCC CTCCATGCAGCCCAAGCCCAGCGGGAGCCTTCCAGCTCGAACTCGTCGCGGGTGTAAATTCTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89687179..89687285 26863196 MeRIP-seq:(Medium) rs944151739 Functional Loss SNV dbSNP153 33..33 33 - - - 79474 RMVar_ID_79474 Human_SNP_ID_614113188 m1A Human chr16 + 89687587 89687587 89687587 TGGCCTTTTCTTTTTTGTTGTTTTTTTGAGACAGGGTCTAGCGCTCTCGCCCAGGCTGGAATGCA TGGCCTTTTCTTTTTTGTTGTTTTTTTGAGACCGGGTCTAGCGCTCTCGCCCAGGCTGGAATGCA A C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89687586..89687949 26863196 MeRIP-seq:(Medium) rs1232860589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12857718,Human_RBP_ID_26952993 79475 RMVar_ID_79475 Human_SNP_ID_614113857 m1A Human chr16 - 89689298 89689298 89689298 ACTCACACACAATGCCGTAGGTACCCTCTCCAATGCGGTTCAGCTTCTCAAACTCCTTCACACTC ACTCACACACAATGCCGTAGGTACCCTCTCCAGTGCGGTTCAGCTTCTCAAACTCCTTCACACTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89689251..89689325 26863196 MeRIP-seq:(Medium) rs746155858 Functional Loss SNV dbSNP153 33..33 33 - - - 79476 RMVar_ID_79476 Human_SNP_ID_614114204 m1A Human chr16 + 89690326 89690326 89690326 GAACTGAGTGGCTGGAGGCCAGGGTCCAGCACAGAGCAAAGTTGGGCACCCCCTGCCCAGTTCAA GAACTGAGTGGCTGGAGGCCAGGGTCCAGCACGGAGCAAAGTTGGGCACCCCCTGCCCAGTTCAA A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89690323..89690424 32194978 MeRIP-seq:(Medium) rs1567514002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25596,RMVar_hsa_circ_342359,RMVar_hsa_circ_370076,RMVar_hsa_circ_322447,RMVar_hsa_circ_328742,RMVar_hsa_circ_53424,RMVar_hsa_circ_180668 79477 RMVar_ID_79477 Human_SNP_ID_614114324 m1A Human chr16 - 89690601 89690601 89690601 CCTGCTCACCATCCTTCTCCTTGTCCATCCGCACCTTCTTCAGTGCGACAATCTCATCTGTCTGG CCTGCTCACCATCCTTCTCCTTGTCCATCCGCGCCTTCTTCAGTGCGACAATCTCATCTGTCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89690386..89690668 26863196 MeRIP-seq:(Medium) rs1567514659 Functional Loss SNV dbSNP153 33..33 33 - - - 79478 RMVar_ID_79478 Human_SNP_ID_614114327 m1A Human chr16 + 89690606 89690606 89690606 CAGATGAGATTGTCGCACTGAAGAAGGTGCGGATGGACAAGGAGAAGGATGGTGAGCAGGAAATT CAGATGAGATTGTCGCACTGAAGAAGGTGCGGGTGGACAAGGAGAAGGATGGTGAGCAGGAAATT A G CDK10 Ensembl:ENSG00000185324 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89690393..89690664;chr16:89690449..89690662 26863196 MeRIP-seq:(Medium) rs904069022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234230,Human_RBP_ID_3949783,Human_RBP_ID_12857836,Human_RBP_ID_26329483 Human_Splice_Rec_1753204,Human_Splice_Rec_1753205,Human_Splice_Rec_1753230,Human_Splice_Rec_1753231,Human_Splice_Rec_1753236,Human_Splice_Rec_1753237,Human_Splice_Rec_1753262,Human_Splice_Rec_1753263,Human_Splice_Rec_1753276,Human_Splice_Rec_1753277,Human_Splice_Rec_1753282,Human_Splice_Rec_1753283,Human_Splice_Rec_1753306,Human_Splice_Rec_1753307,Human_Splice_Rec_1753316,Human_Splice_Rec_1753317,Human_Splice_Rec_1753336,Human_Splice_Rec_1753337,Human_Splice_Rec_1753360,Human_Splice_Rec_1753361,Human_Splice_Rec_1753370,Human_Splice_Rec_1753374,Human_Splice_Rec_1753375,Human_Splice_Rec_1753394,Human_Splice_Rec_1753395,Human_Splice_Rec_1753412,Human_Splice_Rec_1753413,Human_Splice_Rec_1753424,Human_Splice_Rec_1753425,Human_Splice_Rec_1753430,Human_Splice_Rec_1753432,Human_Splice_Rec_1753433,Human_Splice_Rec_1753441,Human_Splice_Rec_1753445 RMVar_hsa_circ_25596,RMVar_hsa_circ_342359,RMVar_hsa_circ_370076,RMVar_hsa_circ_322447,RMVar_hsa_circ_328742,RMVar_hsa_circ_53424,RMVar_hsa_circ_53328,RMVar_hsa_circ_306039,RMVar_hsa_circ_180668,RMVar_hsa_circ_378933,RMVar_hsa_circ_283106,RMVar_hsa_circ_180669 79479 RMVar_ID_79479 Human_SNP_ID_614114815 m1A Human chr16 - 89691817 89691817 89691817 GGCTGGCCAGGTCCTGCTCACAGTAACCCATCACCAGGAAGATGCTGGAAGAAACAGAAGATGCA GGCTGGCCAGGTCCTGCTCACAGTAACCCATCGCCAGGAAGATGCTGGAAGAAACAGAAGATGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89690572..89692550 32194978 MeRIP-seq:(Medium) rs778742347 Functional Loss SNV dbSNP153 33..33 33 - - - 79480 RMVar_ID_79480 Human_SNP_ID_614115546 m1A Human chr16 + 89693432 89693432 89693432 GATTTCGGCCTGGCCCGGGCCTATGGTGTCCCAGTAAAGCCAATGACCCCCAAGGTGGTCACTCT GATTTCGGCCTGGCCCGGGCCTATGGTGTCCCGGTAAAGCCAATGACCCCCAAGGTGGTCACTCT A G CDK10 Ensembl:ENSG00000185324 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89693289..89693690 32194978 MeRIP-seq:(Medium) rs768569643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482093,Human_RBP_ID_2490969,Human_RBP_ID_20164520,Human_RBP_ID_26329486 Human_Splice_Rec_1753214,Human_Splice_Rec_1753215,Human_Splice_Rec_1753246,Human_Splice_Rec_1753247,Human_Splice_Rec_1753292,Human_Splice_Rec_1753293,Human_Splice_Rec_1753325,Human_Splice_Rec_1753346,Human_Splice_Rec_1753347,Human_Splice_Rec_1753404,Human_Splice_Rec_1753405,Human_Splice_Rec_1753454,Human_Splice_Rec_1753455,Human_Splice_Rec_1753470,Human_Splice_Rec_1753471 Human_miRNA_ID_2938945 RMVar_hsa_circ_25596,RMVar_hsa_circ_328742,RMVar_hsa_circ_53424,RMVar_hsa_circ_378933,RMVar_hsa_circ_114897,RMVar_hsa_circ_297948,RMVar_hsa_circ_180671,RMVar_hsa_circ_180672 79481 RMVar_ID_79481 Human_SNP_ID_614115706 m1A Human chr16 + 89693856 89693855 89693857 AACAGGGTCATGCTTAGCCAGGGCTGAATATCAGAGTTGGTCAGAATCAGGTCAGGACCCCAGTG AACAGGGTCATGCTTAGCCAGGGCTGAATATC__AGTTGGTCAGAATCAGGTCAGGACCCCAGTG CAG C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89693839..89694339 32194978 MeRIP-seq:(Medium) rs1461074916 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_45676,Human_RBP_ID_1848018,Human_RBP_ID_3501802,Human_RBP_ID_5356192,Human_RBP_ID_12857872,Human_RBP_ID_22943813,Human_RBP_ID_23707674 RMVar_hsa_circ_25596,RMVar_hsa_circ_53424,RMVar_hsa_circ_297948,RMVar_hsa_circ_180671 79482 RMVar_ID_79482 Human_SNP_ID_614115812 m1A Human chr16 + 89694137 89694137 89694137 GTGTCCTGTGGAGGCCTGGGCTGGGGGAGAGGAGCCGGCTGTATTGAGGTGGGTGCTTCTGTGTG GTGTCCTGTGGAGGCCTGGGCTGGGGGAGAGGGGCCGGCTGTATTGAGGTGGGTGCTTCTGTGTG A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89694086..89694212 26863196 MeRIP-seq:(Medium) rs770870597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889141,Human_RBP_ID_1526964,Human_RBP_ID_3948181,Human_RBP_ID_5318141,Human_RBP_ID_5357055,Human_RBP_ID_17122111,Human_RBP_ID_21972106,Human_RBP_ID_22583344,Human_RBP_ID_22652627,Human_RBP_ID_26768969 Human_Splice_Rec_1753217,Human_Splice_Rec_1753249,Human_Splice_Rec_1753295,Human_Splice_Rec_1753327,Human_Splice_Rec_1753349,Human_Splice_Rec_1753383,Human_Splice_Rec_1753407,Human_Splice_Rec_1753457,Human_Splice_Rec_1753475 RMVar_hsa_circ_25596,RMVar_hsa_circ_53424,RMVar_hsa_circ_297948,RMVar_hsa_circ_180671 79483 RMVar_ID_79483 Human_SNP_ID_614116173 m1A Human chr16 + 89694727 89694727 89694727 GGCGCACAGGCCTCTTCTCCCCGGCACTTCCGAGATCCACCAGATCGACTTGATCGTGCAGCTGC GGCGCACAGGCCTCTTCTCCCCGGCACTTCCGGGATCCACCAGATCGACTTGATCGTGCAGCTGC A G CDK10 Ensembl:ENSG00000185324 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89694438..89694994 32194978 MeRIP-seq:(Medium) rs1245885264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482098,Human_RBP_ID_18687738 Human_Splice_Rec_1753218,Human_Splice_Rec_1753219,Human_Splice_Rec_1753250,Human_Splice_Rec_1753251,Human_Splice_Rec_1753296,Human_Splice_Rec_1753297,Human_Splice_Rec_1753328,Human_Splice_Rec_1753329,Human_Splice_Rec_1753350,Human_Splice_Rec_1753351,Human_Splice_Rec_1753384,Human_Splice_Rec_1753385,Human_Splice_Rec_1753409,Human_Splice_Rec_1753458,Human_Splice_Rec_1753459 RMVar_hsa_circ_19906,RMVar_hsa_circ_25596 79484 RMVar_ID_79484 Human_SNP_ID_614116325 m1A Human chr16 + 89694948 89694948 89694948 TCCTGCCTCCCATAGGGCTTTTCCAAGCTGCCACTGGTCGGCCAGTACAGCCTCCGGAAGCAGCC TCCTGCCTCCCATAGGGCTTTTCCAAGCTGCCCCTGGTCGGCCAGTACAGCCTCCGGAAGCAGCC A C CDK10 Ensembl:ENSG00000185324 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89694898..89695069 26863196 MeRIP-seq:(Medium) rs1371712179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46368,Human_RBP_ID_1526014,Human_RBP_ID_3948184,Human_RBP_ID_18687739,Human_RBP_ID_22052418,Human_RBP_ID_26330445,Human_RBP_ID_26953012 Human_Splice_Rec_1753220,Human_Splice_Rec_1753252,Human_Splice_Rec_1753298,Human_Splice_Rec_1753330,Human_Splice_Rec_1753352,Human_Splice_Rec_1753386,Human_Splice_Rec_1753410,Human_Splice_Rec_1753460,Human_Splice_Rec_1753476 RMVar_hsa_circ_19906,RMVar_hsa_circ_25596 79485 RMVar_ID_79485 Human_SNP_ID_614116326 m1A Human chr16 + 89694948 89694948 89694948 TCCTGCCTCCCATAGGGCTTTTCCAAGCTGCCACTGGTCGGCCAGTACAGCCTCCGGAAGCAGCC TCCTGCCTCCCATAGGGCTTTTCCAAGCTGCCGCTGGTCGGCCAGTACAGCCTCCGGAAGCAGCC A G CDK10 Ensembl:ENSG00000185324 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89694898..89695069 26863196 MeRIP-seq:(Medium) rs1371712179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46368,Human_RBP_ID_1526014,Human_RBP_ID_3948184,Human_RBP_ID_18687739,Human_RBP_ID_22052418,Human_RBP_ID_26330445,Human_RBP_ID_26953012 Human_Splice_Rec_1753220,Human_Splice_Rec_1753252,Human_Splice_Rec_1753298,Human_Splice_Rec_1753330,Human_Splice_Rec_1753352,Human_Splice_Rec_1753386,Human_Splice_Rec_1753410,Human_Splice_Rec_1753460,Human_Splice_Rec_1753476 RMVar_hsa_circ_19906,RMVar_hsa_circ_25596 79486 RMVar_ID_79486 Human_SNP_ID_614117285 m1A Human chr16 - 89696855 89696855 89696855 CACCGAGCTCCCCCCACCCCAAGCTCTGCTGGAGCCAATCTGCGGGGCTCTGCCGGGTGCACGGC CACCGAGCTCCCCCCACCCCAAGCTCTGCTGGGGCCAATCTGCGGGGCTCTGCCGGGTGCACGGC T C SPATA2L Ensembl:ENSG00000158792 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs462769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1753494 GWAS_ID_9534,GWAS_ID_9535,GWAS_ID_9536,GWAS_ID_9537,GWAS_ID_9538,GWAS_ID_9539,GWAS_ID_9540,GWAS_ID_9541 RMVar_hsa_circ_180673,RMVar_hsa_circ_107430 79487 RMVar_ID_79487 Human_SNP_ID_614122463 m1A Human chr16 - 89709375 89709375 89709375 CTGAGCAGGAGCATGGAGCTCTACAGGAATGCACCCCCCACCGCCATTGGCATCCCCACCAAGCT CTGAGCAGGAGCATGGAGCTCTACAGGAATGCCCCCCCCACCGCCATTGGCATCCCCACCAAGCT T G VPS9D1 Ensembl:ENSG00000075399 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89709325..89709393 26863196 MeRIP-seq:(Medium) rs1354102571 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1753516,Human_Splice_Rec_1753542,Human_Splice_Rec_1753552 RMVar_hsa_circ_180674,RMVar_hsa_circ_100285,RMVar_hsa_circ_111009,RMVar_hsa_circ_180675,RMVar_hsa_circ_123285,RMVar_hsa_circ_180676 79488 RMVar_ID_79488 Human_SNP_ID_614123095 m1A Human chr16 - 89710818 89710818 89710818 CATTGCATGCTGTCCCCGCCCGAGCCCAGCGCAGCCCCGCGGCCCCAGGACAGTCCCCCCACGCC CATTGCATGCTGTCCCCGCCCGAGCCCAGCGCTGCCCCGCGGCCCCAGGACAGTCCCCCCACGCC T A VPS9D1 Ensembl:ENSG00000075399 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89710699..89710941 26863196 MeRIP-seq:(Medium) rs544856270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892909,Human_RBP_ID_17079032,Human_RBP_ID_21971703 Human_miRNA_ID_2040992,Human_miRNA_ID_3019976,Human_miRNA_ID_3066198 RMVar_hsa_circ_180674,RMVar_hsa_circ_100285,RMVar_hsa_circ_111009,RMVar_hsa_circ_180675,RMVar_hsa_circ_50053,RMVar_hsa_circ_123285,RMVar_hsa_circ_180676 79489 RMVar_ID_79489 Human_SNP_ID_614123113 m1A Human chr16 - 89710875 89710859 89710875 TGCTGCCCCCCGACCCCCAACCCCGGAAGCCGACGGCTGCGGCCCTCGCAGAGCCTCCATTGCAT TGCTGCCCCCCGACCCCCAACCCCGGAAGCCG________________CAGAGCCTCCATTGCAT GCGAGGGCCGCAGCCGT G VPS9D1 Ensembl:ENSG00000075399 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89710826..89710946 26863196 MeRIP-seq:(Medium) rs768003404 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_21971704 RMVar_hsa_circ_180674,RMVar_hsa_circ_100285,RMVar_hsa_circ_111009,RMVar_hsa_circ_180675,RMVar_hsa_circ_50053,RMVar_hsa_circ_123285,RMVar_hsa_circ_180676 79490 RMVar_ID_79490 Human_SNP_ID_614123700 m1A Human chr16 + 89711915 89711915 89711915 TGGTCCTGTTCGTACTCCAGGATGGCGGCGTAAAGGGCCCGCTGCTCCCGTTCCTCCGGGGTCAG TGGTCCTGTTCGTACTCCAGGATGGCGGCGTACAGGGCCCGCTGCTCCCGTTCCTCCGGGGTCAG A C VPS9D1-AS1 Ensembl:ENSG00000261373 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89711876..89712042 26863196 MeRIP-seq:(Medium) rs754429440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816408,Human_RBP_ID_4394122,Human_RBP_ID_5574797,Human_RBP_ID_8443165 79491 RMVar_ID_79491 Human_SNP_ID_614123735 m1A Human chr16 - 89711968 89711968 89711968 CCCGGCACCCACCGCGTGCCTTTCTCCCCAGGAGGTTTTGCAGCCAAGTCGCCCTGACCCCGGAG CCCGGCACCCACCGCGTGCCTTTCTCCCCAGGTGGTTTTGCAGCCAAGTCGCCCTGACCCCGGAG T A VPS9D1 Ensembl:ENSG00000075399 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89711947..89712060;chr16:89711935..89712153 26863196 MeRIP-seq:(Medium) rs1296312804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1753508,Human_Splice_Rec_1753509,Human_Splice_Rec_1753534,Human_Splice_Rec_1753535,Human_Splice_Rec_1753562,Human_Splice_Rec_1753563,Human_Splice_Rec_1753574,Human_Splice_Rec_1753575,Human_Splice_Rec_1753582,Human_Splice_Rec_1753583 RMVar_hsa_circ_180674,RMVar_hsa_circ_100285,RMVar_hsa_circ_111009,RMVar_hsa_circ_180675,RMVar_hsa_circ_50053,RMVar_hsa_circ_120543,RMVar_hsa_circ_180677 79492 RMVar_ID_79492 Human_SNP_ID_614123882 m1A Human chr16 - 89712304 89712304 89712304 TCCCCGCTTTGCAGAGGCAGGGTCTCAGGGGAAGGCCCGGCCGCCGTCCCCCATGTTCTCTGGCC TCCCCGCTTTGCAGAGGCAGGGTCTCAGGGGAGGGCCCGGCCGCCGTCCCCCATGTTCTCTGGCC T C VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89712278..89712427 26863196 MeRIP-seq:(Medium) rs112201797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18984519,Human_RBP_ID_21971706 RMVar_hsa_circ_100285,RMVar_hsa_circ_180675,RMVar_hsa_circ_50053,RMVar_hsa_circ_120543,RMVar_hsa_circ_180677 79493 RMVar_ID_79493 Human_SNP_ID_614123884 m1A Human chr16 + 89712314 89712314 89712314 CATGGGGGACGGCGGCCGGGCCTTCCCCTGAGACCCTGCCTCTGCAAAGCGGGGAGCCCCTCGGC CATGGGGGACGGCGGCCGGGCCTTCCCCTGAGGCCCTGCCTCTGCAAAGCGGGGAGCCCCTCGGC A G VPS9D1-AS1 Ensembl:ENSG00000261373 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89712279..89712436 26863196 MeRIP-seq:(Medium) rs935291565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27248844 79494 RMVar_ID_79494 Human_SNP_ID_614124266 m1A Human chr16 + 89713140 89713140 89713140 GGTGATGCAGTGAGCCGAGATCTGGCCACTGCACTCCAGCTGGGGTGATAGAGTGAGACTCTGTC GGTGATGCAGTGAGCCGAGATCTGGCCACTGCGCTCCAGCTGGGGTGATAGAGTGAGACTCTGTC A G VPS9D1-AS1 Ensembl:ENSG00000261373 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1032138885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247514 79495 RMVar_ID_79495 Human_SNP_ID_614125519 m1A Human chr16 - 89716622 89716622 89716622 GCTTGACCCCTGGTTACCCATGGCTTGCAGGGAAAACACGCCTGAAGCCAACCATGCCTGCAGCT GCTTGACCCCTGGTTACCCATGGCTTGCAGGGGAAACACGCCTGAAGCCAACCATGCCTGCAGCT T C VPS9D1 Ensembl:ENSG00000075399 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89716557..89716655 32194978 MeRIP-seq:(Medium) rs746073158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1753502,Human_Splice_Rec_1753528 RMVar_hsa_circ_100285,RMVar_hsa_circ_180675,RMVar_hsa_circ_50053,RMVar_hsa_circ_180679,RMVar_hsa_circ_352462,RMVar_hsa_circ_316657 79496 RMVar_ID_79496 Human_SNP_ID_614125751 m1A Human chr16 + 89717083 89717083 89717083 TGACTGACCCTAGGCAAGCCCACTGCCCCCCCATCCCCTCACCCCGGGTAAGCCCACTGCCCCTT TGACTGACCCTAGGCAAGCCCACTGCCCCCCCCTCCCCTCACCCCGGGTAAGCCCACTGCCCCTT A C VPS9D1-AS1 Ensembl:ENSG00000261373 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89717033..89717193 26863196 MeRIP-seq:(Medium) rs1028516175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482123,Human_RBP_ID_5317093,Human_RBP_ID_17078417,Human_RBP_ID_26953056,Human_RBP_ID_27248866 79497 RMVar_ID_79497 Human_SNP_ID_614125899 m1A Human chr16 + 89717451 89717451 89717451 GTCCCCAAAGTCCTGCCTTCCCGTAGCTTGGCATGGAGCACCTCTGCGCGACCATGGACCTGCTC GTCCCCAAAGTCCTGCCTTCCCGTAGCTTGGCGTGGAGCACCTCTGCGCGACCATGGACCTGCTC A G VPS9D1-AS1 Ensembl:ENSG00000261373 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89717417..89717772 26863196 MeRIP-seq:(Medium) rs973666050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482131,Human_RBP_ID_5184159,Human_RBP_ID_5247624,Human_RBP_ID_5641010,Human_RBP_ID_6550915,Human_RBP_ID_12858219,Human_RBP_ID_22208080,Human_RBP_ID_26953062,Human_RBP_ID_27248872 Human_miRNA_ID_3165761,Human_miRNA_ID_3202948 79498 RMVar_ID_79498 Human_SNP_ID_614125940 m1A Human chr16 - 89717533 89717533 89717533 GGAGGTGGGTCAGGCGCTGGGGCGGTGGGTCCAGGGGCGAGTCACAGAGAGGCAGCTCCCACGGC GGAGGTGGGTCAGGCGCTGGGGCGGTGGGTCCTGGGGCGAGTCACAGAGAGGCAGCTCCCACGGC T A VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89717452..89717657 26863196 MeRIP-seq:(Medium) rs750303390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763379,Human_RBP_ID_816764,Human_RBP_ID_1066164,Human_RBP_ID_3505935,Human_RBP_ID_8185527,Human_RBP_ID_9419496,Human_RBP_ID_17188817,Human_RBP_ID_18939754,Human_RBP_ID_26781027 RMVar_hsa_circ_352462 79499 RMVar_ID_79499 Human_SNP_ID_614125974 m1A Human chr16 - 89717604 89717604 89717604 GAGTCGGGGGCTAAATCGGGGCGGGATGAGAAAATGGGAGTCTATGAGAAGTTTTCTGTGAAGGG GAGTCGGGGGCTAAATCGGGGCGGGATGAGAACATGGGAGTCTATGAGAAGTTTTCTGTGAAGGG T G VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89717393..89717744 26863196 MeRIP-seq:(Medium) rs974018525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18939755 RMVar_hsa_circ_352462 79500 RMVar_ID_79500 Human_SNP_ID_614126262 m1A Human chr16 - 89718030 89717963 89718030 GGGGAGCCACTGGACGTGGGATCACAGAGGTCAGGGGGACCCACTGGACGTGGGAGCACAGAGGT GGGGAGCCACTGGACGTGGGATCACAGAGGTC_________________________________ CGACCTCTGTGCTCCCACGTCCAGTGGCTCCCCCGACCTCTGTGCTCCCACGTCCAGTGGGTCCCCCT C VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89717358..89718467 26863196 MeRIP-seq:(Medium) rs1567553430 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_352462 79501 RMVar_ID_79501 Human_SNP_ID_614126295 m1A Human chr16 - 89718030 89717996 89718030 GGGGAGCCACTGGACGTGGGATCACAGAGGTCAGGGGGACCCACTGGACGTGGGAGCACAGAGGT GGGGAGCCACTGGACGTGGGATCACAGAGGTC_________________________________ CGACCTCTGTGCTCCCACGTCCAGTGGGTCCCCCT C VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89717358..89718467 26863196 MeRIP-seq:(Medium) rs1555525442 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_352462 79502 RMVar_ID_79502 Human_SNP_ID_614126314 m1A Human chr16 - 89718024 89718022 89718024 CCACTGGACGTGGGATCACAGAGGTCAGGGGGACCCACTGGACGTGGGAGCACAGAGGTCGGGGG CCACTGGACGTGGGATCACAGAGGTCAGGGGG__CCACTGGACGTGGGAGCACAGAGGTCGGGGG GGT G VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89717823..89718372 26863196 MeRIP-seq:(Medium) rs1172826949 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_352462 79503 RMVar_ID_79503 Human_SNP_ID_614126322 m1A Human chr16 - 89718030 89718029 89718030 GGGGAGCCACTGGACGTGGGATCACAGAGGTCAGGGGGACCCACTGGACGTGGGAGCACAGAGGT GGGGAGCCACTGGACGTGGGATCACAGAGGTC_GGGGGACCCACTGGACGTGGGAGCACAGAGGT CT C VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89717358..89718467 26863196 MeRIP-seq:(Medium) rs760081750 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_352462 79504 RMVar_ID_79504 Human_SNP_ID_614126323 m1A Human chr16 - 89718030 89718030 89718030 GGGGAGCCACTGGACGTGGGATCACAGAGGTCAGGGGGACCCACTGGACGTGGGAGCACAGAGGT GGGGAGCCACTGGACGTGGGATCACAGAGGTCGGGGGGACCCACTGGACGTGGGAGCACAGAGGT T C VPS9D1 Ensembl:ENSG00000075399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89717358..89718467 26863196 MeRIP-seq:(Medium) rs1200891921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352462 79505 RMVar_ID_79505 Human_SNP_ID_614126412 m1A Human chr16 + 89718211 89718211 89718211 GCCAGTTTGCTCCTGCCCCATCTGCCTCCTGCAAGTCTGCTCTGTTCCACCTTCAGGACGCACCC GCCAGTTTGCTCCTGCCCCATCTGCCTCCTGCCAGTCTGCTCTGTTCCACCTTCAGGACGCACCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89718186..89718379 26863196 MeRIP-seq:(Medium) rs1351302037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482159,Human_RBP_ID_2490979,Human_RBP_ID_5496350,Human_RBP_ID_12858247,Human_RBP_ID_26953076,Human_RBP_ID_27248881,Human_RBP_ID_27447582 79506 RMVar_ID_79506 Human_SNP_ID_614127046 m1A Human chr16 + 89719713 89719713 89719713 CTCTGACAAGGCACAGGTCATTGGAACCACAGAATGGTGGTTTGTTTTGTTTTGTTGAGACAGAG CTCTGACAAGGCACAGGTCATTGGAACCACAGGATGGTGGTTTGTTTTGTTTTGTTGAGACAGAG A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34141697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12858346,Human_RBP_ID_22943835,Human_RBP_ID_26953110,Human_RBP_ID_27248907 GWAS_ID_9542 79507 RMVar_ID_79507 Human_SNP_ID_614127047 m1A Human chr16 + 89719713 89719713 89719713 CTCTGACAAGGCACAGGTCATTGGAACCACAGAATGGTGGTTTGTTTTGTTTTGTTGAGACAGAG CTCTGACAAGGCACAGGTCATTGGAACCACAGTATGGTGGTTTGTTTTGTTTTGTTGAGACAGAG A T - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34141697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12858346,Human_RBP_ID_22943835,Human_RBP_ID_26953110,Human_RBP_ID_27248907 GWAS_ID_9542 79508 RMVar_ID_79508 Human_SNP_ID_614127221 m1A Human chr16 + 89720241 89720241 89720241 TCCCTCCTTGGGCAGCCGGGTGTGGCTGGGCCAGCTTCTCTACCTGGTCGCCAACCTTAGATTCG TCCCTCCTTGGGCAGCCGGGTGTGGCTGGGCCCGCTTCTCTACCTGGTCGCCAACCTTAGATTCG A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs111836360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18687790,Human_RBP_ID_27248914 79509 RMVar_ID_79509 Human_SNP_ID_614127222 m1A Human chr16 + 89720241 89720241 89720241 TCCCTCCTTGGGCAGCCGGGTGTGGCTGGGCCAGCTTCTCTACCTGGTCGCCAACCTTAGATTCG TCCCTCCTTGGGCAGCCGGGTGTGGCTGGGCCGGCTTCTCTACCTGGTCGCCAACCTTAGATTCG A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs111836360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18687790,Human_RBP_ID_27248914 79510 RMVar_ID_79510 Human_SNP_ID_614128368 m1A Human chr16 + 89722649 89722649 89722649 GCGCCTGGAGCGAGCATGGAGAGGCCATCCGCAGAGGAGCGCGTGCTCGTACGGGACTTCCAGCG GCGCCTGGAGCGAGCATGGAGAGGCCATCCGCGGAGGAGCGCGTGCTCGTACGGGACTTCCAGCG A G ZNF276 Ensembl:ENSG00000158805 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89722600..89722751 32194978 MeRIP-seq:(Medium) rs1205390212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892915,Human_RBP_ID_5648062,Human_RBP_ID_9374900,Human_RBP_ID_18984525,Human_RBP_ID_22944760,Human_RBP_ID_26953135,Human_RBP_ID_27248944 RMVar_hsa_circ_117800,RMVar_hsa_circ_118938,RMVar_hsa_circ_180680,RMVar_hsa_circ_24329,RMVar_hsa_circ_53207,RMVar_hsa_circ_180681 79511 RMVar_ID_79511 Human_SNP_ID_614132962 m1A Human chr16 - 89732908 89732906 89732909 GCAGGGTACAGCAGGGTCGGGGTGAACACAGCAGAGGGCGAGGGCGCAGGGTACAGCGGGGTACA GCAGGGTACAGCAGGGTCGGGGTGAACACAG___AGGGCGAGGGCGCAGGGTACAGCGGGGTACA TCTG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89732621..89733095 26863196 MeRIP-seq:(Medium) rs968070707 Functional Loss DEL dbSNP153 32..34 33 - - - 79512 RMVar_ID_79512 Human_SNP_ID_614132976 m1A Human chr16 + 89732924 89732924 89732924 CTGCGCCCTCGCCCTCTGCTGTGTTCACCCCGACCCTGCTGTACCCTGCGCCCTCATCCTCTGCT CTGCGCCCTCGCCCTCTGCTGTGTTCACCCCGCCCCTGCTGTACCCTGCGCCCTCATCCTCTGCT A C ZNF276 Ensembl:ENSG00000158805 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr16:89732793..89733050;chr16:89732637..89733011 26863196 MeRIP-seq:(Medium) rs1318960152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128307,Human_RBP_ID_18939762,Human_RBP_ID_22474645 RMVar_hsa_circ_24329,RMVar_hsa_circ_35119,RMVar_hsa_circ_351225 79513 RMVar_ID_79513 Human_SNP_ID_614133382 m1A Human chr16 - 89733545 89733545 89733545 CAGGCACAGCCAGTGCTCACCTTCATGCCGTCAGCGCCTCGGTACACGGCCGTGCAGCCCTGGTA CAGGCACAGCCAGTGCTCACCTTCATGCCGTCGGCGCCTCGGTACACGGCCGTGCAGCCCTGGTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89733427..89733990 32194978 MeRIP-seq:(Medium) rs1337488115 Functional Loss SNV dbSNP153 33..33 33 - - - 79514 RMVar_ID_79514 Human_SNP_ID_614135489 m1A Human chr16 - 89737863 89737863 89737863 TGGCTCCCGAATGTCGCATTTGGTGGACGAGAAGGTGCTTCCGCTGCTTGAAGGTTTGTCCACAT TGGCTCCCGAATGTCGCATTTGGTGGACGAGAGGGTGCTTCCGCTGCTTGAAGGTTTGTCCACAT T C FANCA Ensembl:ENSG00000187741 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89737812..89737913 32194978 MeRIP-seq:(Medium) rs1277811616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482199 79515 RMVar_ID_79515 Human_SNP_ID_614135512 m1A Human chr16 - 89737907 89737904 89737908 ACAGCCCTGGGAGGGGGTCCTGACTCACACTTACTGCAAAGGCTTGGCTCCCGAATGTCGCATTT ACAGCCCTGGGAGGGGGTCCTGACTCACACT____GCAAAGGCTTGGCTCCCGAATGTCGCATTT CAGTA C FANCA Ensembl:ENSG00000187741 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89737894..89738018 26863196 MeRIP-seq:(Medium) rs753790953 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_27447625 79516 RMVar_ID_79516 Human_SNP_ID_614136017 m1A Human chr16 + 89738707 89738707 89738707 CCTCTGGGTCGCAGTCCCCACGATCAGCCAGCAGCTGTGAGAGAGGAGCAGGTCCTCAGCCCATG CCTCTGGGTCGCAGTCCCCACGATCAGCCAGCGGCTGTGAGAGAGGAGCAGGTCCTCAGCCCATG A G ZNF276 Ensembl:ENSG00000158805 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89738659..89738810 32194978 MeRIP-seq:(Medium) rs761987751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26757600,Human_RBP_ID_26781034 79517 RMVar_ID_79517 Human_SNP_ID_614136621 m1A Human chr16 - 89739611 89739611 89739611 GGGTACACGTCCCGACCCCCAGGGGTGTCCCCAGCACTGATAATAGGCAGAGATGTCCAGAGTTG GGGTACACGTCCCGACCCCCAGGGGTGTCCCCGGCACTGATAATAGGCAGAGATGTCCAGAGTTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89739576..89739724 26863196 MeRIP-seq:(Medium) rs1353743360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128939,Human_RBP_ID_17077760,Human_RBP_ID_22542658 RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_90602,RMVar_hsa_circ_113715,RMVar_hsa_circ_180686,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689 79518 RMVar_ID_79518 Human_SNP_ID_614136640 m1A Human chr16 - 89739637 89739637 89739637 CACTATCCCCACAGCCAGGCCTCCCAGGGTACACGTCCCGACCCCCAGGGGTGTCCCCAGCACTG CACTATCCCCACAGCCAGGCCTCCCAGGGTACTCGTCCCGACCCCCAGGGGTGTCCCCAGCACTG T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89739586..89739742 26863196 MeRIP-seq:(Medium) rs949700788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128939,Human_RBP_ID_17077760 RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_90602,RMVar_hsa_circ_113715,RMVar_hsa_circ_180686,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689 79519 RMVar_ID_79519 Human_SNP_ID_614136650 m1A Human chr16 - 89739665 89739665 89739665 GTATCCTCAGCTCAGGCTGTTCGCCCCACACTATCCCCACAGCCAGGCCTCCCAGGGTACACGTC GTATCCTCAGCTCAGGCTGTTCGCCCCACACTGTCCCCACAGCCAGGCCTCCCAGGGTACACGTC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89739634..89739771 26863196 MeRIP-seq:(Medium) rs1319945656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128939,Human_RBP_ID_17077760,Human_RBP_ID_22583356 RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_90602,RMVar_hsa_circ_113715,RMVar_hsa_circ_180686,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689 79520 RMVar_ID_79520 Human_SNP_ID_614164678 m1A Human chr16 + 89804453 89804453 89804453 GGCGGTTCTCTAGAGCTGTCCTGCCGCCGTCCAGGAGTGCGCTGAATATAAGTCCTGACAAACCC GGCGGTTCTCTAGAGCTGTCCTGCCGCCGTCCGGGAGTGCGCTGAATATAAGTCCTGACAAACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89804451..89804582 26863196 MeRIP-seq:(Medium) rs962551467 Functional Loss SNV dbSNP153 33..33 33 - - - 79521 RMVar_ID_79521 Human_SNP_ID_614165070 m1A Human chr16 - 89805330 89805330 89805330 GCTCTTCAGGAATCTGTGCTGCCTTTGTGAACAGATGGAAGCATCCTGCCAGCATGCTGACGTCG GCTCTTCAGGAATCTGTGCTGCCTTTGTGAACTGATGGAAGCATCCTGCCAGCATGCTGACGTCG T A FANCA Ensembl:ENSG00000187741 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89805250..89805333 26863196 MeRIP-seq:(Medium) rs537435838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45746,Human_RBP_ID_892954,Human_RBP_ID_1089243,Human_RBP_ID_1526360,Human_RBP_ID_1848132,Human_RBP_ID_8443337,Human_RBP_ID_9373462,Human_RBP_ID_12860785,Human_RBP_ID_18688043,Human_RBP_ID_18984582,Human_RBP_ID_19076406,Human_RBP_ID_22802816,Human_RBP_ID_22944038,Human_RBP_ID_26328300 Human_Splice_Rec_1753760,Human_Splice_Rec_1753761,Human_Splice_Rec_1753838,Human_Splice_Rec_1753839,Human_Splice_Rec_1754064,Human_Splice_Rec_1754065,Human_Splice_Rec_1754090,Human_Splice_Rec_1754091,Human_Splice_Rec_1754110,Human_Splice_Rec_1754111,Human_Splice_Rec_1754130,Human_Splice_Rec_1754131,Human_Splice_Rec_1754148,Human_Splice_Rec_1754149,Human_Splice_Rec_1754166,Human_Splice_Rec_1754167,Human_Splice_Rec_1754184,Human_Splice_Rec_1754185 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180691,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_110423,RMVar_hsa_circ_89693,RMVar_hsa_circ_180740,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_35741,RMVar_hsa_circ_21024,RMVar_hsa_circ_102907,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_111171,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_29735,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180759,RMVar_hsa_circ_180758,RMVar_hsa_circ_118243,RMVar_hsa_circ_314291,RMVar_hsa_circ_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_180766,RMVar_hsa_circ_60302,RMVar_hsa_circ_281399,RMVar_hsa_circ_11673,RMVar_hsa_circ_180768,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 79522 RMVar_ID_79522 Human_SNP_ID_614165071 m1A Human chr16 - 89805330 89805330 89805330 GCTCTTCAGGAATCTGTGCTGCCTTTGTGAACAGATGGAAGCATCCTGCCAGCATGCTGACGTCG GCTCTTCAGGAATCTGTGCTGCCTTTGTGAACCGATGGAAGCATCCTGCCAGCATGCTGACGTCG T G FANCA Ensembl:ENSG00000187741 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89805250..89805333 26863196 MeRIP-seq:(Medium) rs537435838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45746,Human_RBP_ID_892954,Human_RBP_ID_1089243,Human_RBP_ID_1526360,Human_RBP_ID_1848132,Human_RBP_ID_8443337,Human_RBP_ID_9373462,Human_RBP_ID_12860785,Human_RBP_ID_18688043,Human_RBP_ID_18984582,Human_RBP_ID_19076406,Human_RBP_ID_22802816,Human_RBP_ID_22944038,Human_RBP_ID_26328300 Human_Splice_Rec_1753760,Human_Splice_Rec_1753761,Human_Splice_Rec_1753838,Human_Splice_Rec_1753839,Human_Splice_Rec_1754064,Human_Splice_Rec_1754065,Human_Splice_Rec_1754090,Human_Splice_Rec_1754091,Human_Splice_Rec_1754110,Human_Splice_Rec_1754111,Human_Splice_Rec_1754130,Human_Splice_Rec_1754131,Human_Splice_Rec_1754148,Human_Splice_Rec_1754149,Human_Splice_Rec_1754166,Human_Splice_Rec_1754167,Human_Splice_Rec_1754184,Human_Splice_Rec_1754185 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180691,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_110423,RMVar_hsa_circ_89693,RMVar_hsa_circ_180740,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_35741,RMVar_hsa_circ_21024,RMVar_hsa_circ_102907,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_111171,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_29735,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180759,RMVar_hsa_circ_180758,RMVar_hsa_circ_118243,RMVar_hsa_circ_314291,RMVar_hsa_circ_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_180766,RMVar_hsa_circ_60302,RMVar_hsa_circ_281399,RMVar_hsa_circ_11673,RMVar_hsa_circ_180768,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 79523 RMVar_ID_79523 Human_SNP_ID_614166716 m1A Human chr16 - 89808640 89808640 89808640 CTGTGTTGGCTGTAGTGTGGAGAAAGGGTTAGAAGTAGGCTACAGTGCGTAGGAAGAGAGAAGGA CTGTGTTGGCTGTAGTGTGGAGAAAGGGTTAGGAGTAGGCTACAGTGCGTAGGAAGAGAGAAGGA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89808589..89808695 26863196 MeRIP-seq:(Medium) rs1440015844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860868,Human_RBP_ID_22944054,Human_RBP_ID_23707860 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_124924,RMVar_hsa_circ_180691,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_112173,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_110423,RMVar_hsa_circ_89693,RMVar_hsa_circ_180740,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_21024,RMVar_hsa_circ_102907,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180758,RMVar_hsa_circ_11673,RMVar_hsa_circ_377504 79524 RMVar_ID_79524 Human_SNP_ID_614166721 m1A Human chr16 - 89808648 89808648 89808648 GTGTAATACTGTGTTGGCTGTAGTGTGGAGAAAGGGTTAGAAGTAGGCTACAGTGCGTAGGAAGA GTGTAATACTGTGTTGGCTGTAGTGTGGAGAATGGGTTAGAAGTAGGCTACAGTGCGTAGGAAGA T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89808598..89808707 26863196 MeRIP-seq:(Medium) rs1278690508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860868,Human_RBP_ID_22944054,Human_RBP_ID_23707861 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_124924,RMVar_hsa_circ_180691,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_112173,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_110423,RMVar_hsa_circ_89693,RMVar_hsa_circ_180740,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_21024,RMVar_hsa_circ_102907,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180758,RMVar_hsa_circ_11673,RMVar_hsa_circ_377504 79525 RMVar_ID_79525 Human_SNP_ID_614170260 m1A Human chr16 + 89815955 89815955 89815955 ACAGCTGATTCCTTTAATTTCTGTGCCCTTTCAGGATTATATTTTTCCCTCTTGACCCTTCCCGC ACAGCTGATTCCTTTAATTTCTGTGCCCTTTCGGGATTATATTTTTCCCTCTTGACCCTTCCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89814594..89816043 26863196 MeRIP-seq:(Medium) rs936941432 Functional Loss SNV dbSNP153 33..33 33 - - - 79526 RMVar_ID_79526 Human_SNP_ID_614170707 m1A Human chr16 + 89816603 89816603 89816603 TGGGTCCTGGCCCGAGGCGGAGTTCGGGACCCACGAGTCGGACATGGCCTTGGCGCCTACAGCCC TGGGTCCTGGCCCGAGGCGGAGTTCGGGACCCGCGAGTCGGACATGGCCTTGGCGCCTACAGCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr16:89816468..89816650;chr16:89816476..89816650 26863196 MeRIP-seq:(Medium) rs1204745684 Functional Loss SNV dbSNP153 33..33 33 - - - 79527 RMVar_ID_79527 Human_SNP_ID_614175208 m1A Human chr16 - 89828288 89828288 89828288 TGAGGGGCAGGGCGGGGCGCGGGTAGGTGCGGAGGGGCTGGGGCTCAGGGCTGGGGACGCGGGGG TGAGGGGCAGGGCGGGGCGCGGGTAGGTGCGGTGGGGCTGGGGCTCAGGGCTGGGGACGCGGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89828237..89828308 26863196 MeRIP-seq:(Medium) rs1377000615 Functional Loss SNV dbSNP153 33..33 33 - - - 79528 RMVar_ID_79528 Human_SNP_ID_614175379 m1A Human chr16 - 89828569 89828569 89828569 CGGCCGCCCTGCGCCCGCCGCGGCGCCGCCGCAGCTGCCCGCCCGGGCCATGGCGGGGCCGTCAT CGGCCGCCCTGCGCCCGCCGCGGCGCCGCCGCCGCTGCCCGCCCGGGCCATGGCGGGGCCGTCAT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:89828498..89828600 26863410 MeRIP-seq:(Medium) rs1408017445 Functional Loss SNV dbSNP153 33..33 33 - - - 79529 RMVar_ID_79529 Human_SNP_ID_614181615 m1A Human chr16 + 89845364 89845364 89845364 CATGGTCGTGCCACTAGCCAGCTCGGAAGCCCAGGTACTTTTTAAAAAATTCCAAGTATTACTTG CATGGTCGTGCCACTAGCCAGCTCGGAAGCCCCGGTACTTTTTAAAAAATTCCAAGTATTACTTG A C SPIRE2 Ensembl:ENSG00000204991 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89836406..89845755 26863196 MeRIP-seq:(Medium) rs1282501609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18984590,Human_RBP_ID_25241909 Human_Splice_Rec_1754216,Human_Splice_Rec_1754217,Human_Splice_Rec_1754222,Human_Splice_Rec_1754223,Human_Splice_Rec_1754248,Human_Splice_Rec_1754249,Human_Splice_Rec_1754270,Human_Splice_Rec_1754271,Human_Splice_Rec_1754276,Human_Splice_Rec_1754277 RMVar_hsa_circ_12927,RMVar_hsa_circ_38635,RMVar_hsa_circ_180770,RMVar_hsa_circ_94298,RMVar_hsa_circ_75360,RMVar_hsa_circ_45727,RMVar_hsa_circ_180771 79530 RMVar_ID_79530 Human_SNP_ID_614181616 m1A Human chr16 + 89845364 89845364 89845364 CATGGTCGTGCCACTAGCCAGCTCGGAAGCCCAGGTACTTTTTAAAAAATTCCAAGTATTACTTG CATGGTCGTGCCACTAGCCAGCTCGGAAGCCCGGGTACTTTTTAAAAAATTCCAAGTATTACTTG A G SPIRE2 Ensembl:ENSG00000204991 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89836406..89845755 26863196 MeRIP-seq:(Medium) rs1282501609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18984590,Human_RBP_ID_25241909 Human_Splice_Rec_1754216,Human_Splice_Rec_1754217,Human_Splice_Rec_1754222,Human_Splice_Rec_1754223,Human_Splice_Rec_1754248,Human_Splice_Rec_1754249,Human_Splice_Rec_1754270,Human_Splice_Rec_1754271,Human_Splice_Rec_1754276,Human_Splice_Rec_1754277 RMVar_hsa_circ_12927,RMVar_hsa_circ_38635,RMVar_hsa_circ_180770,RMVar_hsa_circ_94298,RMVar_hsa_circ_75360,RMVar_hsa_circ_45727,RMVar_hsa_circ_180771 79531 RMVar_ID_79531 Human_SNP_ID_614184587 m1A Human chr16 - 89852883 89852849 89852883 CGGAAGACGGGCCATGGGATCCGGGGGGTGAGAGGGAGGACGGAAGAGGGGCCATGGGATGCGGG CGGAAGACGGGCCATGGGATCCGGGGGGTGAG_________________________________ CCCCCGCATCCCATGGCCCCTCTTCCGTCCTCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89852882..89853008 26863196 MeRIP-seq:(Medium) rs1186335151 Functional Loss DEL dbSNP153 33..65 33 - - - 79532 RMVar_ID_79532 Human_SNP_ID_614188373 m1A Human chr16 + 89863181 89863181 89863181 GGCTGGTGTGGATCAGCCCATGGTGTGTTTGCAGGCAGGGACACCTTGAACAGACATGGGCTGAG GGCTGGTGTGGATCAGCCCATGGTGTGTTTGCGGGCAGGGACACCTTGAACAGACATGGGCTGAG A G SPIRE2 Ensembl:ENSG00000204991 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89863156..89863367 26863196 MeRIP-seq:(Medium) rs1393056023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23707924 RMVar_hsa_circ_80102,RMVar_hsa_circ_12927,RMVar_hsa_circ_180770,RMVar_hsa_circ_94298,RMVar_hsa_circ_109106,RMVar_hsa_circ_81638,RMVar_hsa_circ_180773,RMVar_hsa_circ_98929,RMVar_hsa_circ_180774,RMVar_hsa_circ_180775,RMVar_hsa_circ_180776 79533 RMVar_ID_79533 Human_SNP_ID_614190878 m1A Human chr16 + 89870230 89870230 89870230 AACACTACGCCACGACGCAGTCGCCAGACCCAATCCCTCTACATCCCTAACACCAGGACTCTTGA AACACTACGCCACGACGCAGTCGCCAGACCCAGTCCCTCTACATCCCTAACACCAGGACTCTTGA A G SPIRE2 Ensembl:ENSG00000204991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89870179..89870297 26863196 MeRIP-seq:(Medium) rs766056379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371092,Human_RBP_ID_27249116,Human_RBP_ID_27447683 RMVar_hsa_circ_80102,RMVar_hsa_circ_180770,RMVar_hsa_circ_94298,RMVar_hsa_circ_109106,RMVar_hsa_circ_81638,RMVar_hsa_circ_180773,RMVar_hsa_circ_98929,RMVar_hsa_circ_180774,RMVar_hsa_circ_180775,RMVar_hsa_circ_180776 79534 RMVar_ID_79534 Human_SNP_ID_614192176 m1A Human chr16 + 89873668 89873668 89873668 CCTCTCTCCAGACGTCGTGGTCGTTCGGTCCTATGTCGCGCCGGGCCCTCCGGAGGCTGAGGGGG CCTCTCTCCAGACGTCGTGGTCGTTCGGTCCTGTGTCGCGCCGGGCCCTCCGGAGGCTGAGGGGG A G TCF25 Ensembl:ENSG00000141002 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89873632..89873769 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_44937,Human_RBP_ID_4405054,Human_RBP_ID_8726437,Human_RBP_ID_18688145,Human_RBP_ID_22208448,Human_RBP_ID_26953449,Human_RBP_ID_27812108 RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779 79535 RMVar_ID_79535 Human_SNP_ID_614192279 m1A Human chr16 + 89873824 89873824 89873824 AGCTTGGTGTCCGGCGTCCCGGGGGCGCAGGGAAGGAGGGCGTCCGAGTCAACAACCGCTTCGAG AGCTTGGTGTCCGGCGTCCCGGGGGCGCAGGGCAGGAGGGCGTCCGAGTCAACAACCGCTTCGAG A C TCF25 Ensembl:ENSG00000141002 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:89873776..89873969 26863196 MeRIP-seq:(Medium) rs13338056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818417,Human_RBP_ID_3948224,Human_RBP_ID_18987427,Human_RBP_ID_22441195,Human_RBP_ID_26329502,Human_RBP_ID_27812109 Human_Splice_Rec_1754331,Human_Splice_Rec_1754369,Human_Splice_Rec_1754405,Human_Splice_Rec_1754407,Human_Splice_Rec_1754441,Human_Splice_Rec_1754453,Human_Splice_Rec_1754463,Human_Splice_Rec_1754465,Human_Splice_Rec_1754477,Human_Splice_Rec_1754485 RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779 79536 RMVar_ID_79536 Human_SNP_ID_614192288 m1A Human chr16 - 89873834 89873834 89873834 TCCTCACCAGCTCGAAGCGGTTGTTGACTCGGACGCCCTCCTTCCCTGCGCCCCCGGGACGCCGG TCCTCACCAGCTCGAAGCGGTTGTTGACTCGGCCGCCCTCCTTCCCTGCGCCCCCGGGACGCCGG T G lnc-FANCA-3 RNACentral:URS0000D57DB2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:89873626..89874018;chr16:89873619..89874559 26863196 MeRIP-seq:(Medium) rs373492730 Functional Loss SNV dbSNP153 33..33 33 - - - 79537 RMVar_ID_79537 Human_SNP_ID_614196388 m1A Human chr16 + 89884639 89884639 89884639 AGAAGAAAAAAAAACAGAAAAACAAGAAAAGCAGCACGGGAGAAGCATCGGTACGTGAGTTGGGC AGAAGAAAAAAAAACAGAAAAACAAGAAAAGCGGCACGGGAGAAGCATCGGTACGTGAGTTGGGC A G TCF25 Ensembl:ENSG00000141002 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89884542..89884711 26863196 MeRIP-seq:(Medium) rs201815902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892964,Human_RBP_ID_22583388,Human_RBP_ID_24544456 Human_Splice_Rec_1754334,Human_Splice_Rec_1754335,Human_Splice_Rec_1754372,Human_Splice_Rec_1754373,Human_Splice_Rec_1754410,Human_Splice_Rec_1754411,Human_Splice_Rec_1754444,Human_Splice_Rec_1754445,Human_Splice_Rec_1754456,Human_Splice_Rec_1754457,Human_Splice_Rec_1754470,Human_Splice_Rec_1754471,Human_Splice_Rec_1754480,Human_Splice_Rec_1754481,Human_Splice_Rec_1754488,Human_Splice_Rec_1754489,Human_Splice_Rec_1754504,Human_Splice_Rec_1754506,Human_Splice_Rec_1754507,Human_Splice_Rec_1754509,Human_Splice_Rec_1754517 RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_74372,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779,RMVar_hsa_circ_329545,RMVar_hsa_circ_180781,RMVar_hsa_circ_302840,RMVar_hsa_circ_180780,RMVar_hsa_circ_338617,RMVar_hsa_circ_271362,RMVar_hsa_circ_180787,RMVar_hsa_circ_180783,RMVar_hsa_circ_180784,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_359033,RMVar_hsa_circ_180786 79538 RMVar_ID_79538 Human_SNP_ID_614199897 m1A Human chr16 - 89894219 89894209 89894220 CCGGGGCCGTGTGGGGGCCGTCCGGGGGCTGCACGGGGGCCGGGAATCTGAGCTGCTCGCCTGCA CCGGGGCCGTGTGGGGGCCGTCCGGGGGCTG___________GGAATCTGAGCTGCTCGCCTGCA CCGGCCCCCGTG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:89894199..89894364 26863196 MeRIP-seq:(Medium) rs931443884 Functional Loss DEL dbSNP153 32..42 33 - - - 79539 RMVar_ID_79539 Human_SNP_ID_614199927 m1A Human chr16 + 89894275 89894244 89894275 CGGCCCCGGACGGCCCCCGCGCAGCCCCAGACAGCCCCGGACCTGGACAGTCCCCGTACAGCCCC CG_______________________________GCCCCGGACCTGGACAGTCCCCGTACAGCCCC GGCCCCGGACGGCCCCCGCGCAGCCCCAGACA G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89894268..89894371 26863196 MeRIP-seq:(Medium) rs1048474621 Functional Loss DEL dbSNP153 3..33 33 - - - Human_RBP_ID_12862312 RMVar_hsa_circ_1394,RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_302840,RMVar_hsa_circ_122823,RMVar_hsa_circ_180787,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180790,RMVar_hsa_circ_275870,RMVar_hsa_circ_287198,RMVar_hsa_circ_342629,RMVar_hsa_circ_372753,RMVar_hsa_circ_334753,RMVar_hsa_circ_279639,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_76931,RMVar_hsa_circ_180795,RMVar_hsa_circ_180797,RMVar_hsa_circ_180798,RMVar_hsa_circ_180796,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_180800,RMVar_hsa_circ_180801 79540 RMVar_ID_79540 Human_SNP_ID_614199946 m1A Human chr16 + 89894275 89894275 89894275 CGGCCCCGGACGGCCCCCGCGCAGCCCCAGACAGCCCCGGACCTGGACAGTCCCCGTACAGCCCC CGGCCCCGGACGGCCCCCGCGCAGCCCCAGACTGCCCCGGACCTGGACAGTCCCCGTACAGCCCC A T TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89894268..89894371 26863196 MeRIP-seq:(Medium) rs953075948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12862312 RMVar_hsa_circ_1394,RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_302840,RMVar_hsa_circ_122823,RMVar_hsa_circ_180787,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180790,RMVar_hsa_circ_275870,RMVar_hsa_circ_287198,RMVar_hsa_circ_342629,RMVar_hsa_circ_372753,RMVar_hsa_circ_334753,RMVar_hsa_circ_279639,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_76931,RMVar_hsa_circ_180795,RMVar_hsa_circ_180797,RMVar_hsa_circ_180798,RMVar_hsa_circ_180796,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_180800,RMVar_hsa_circ_180801 79541 RMVar_ID_79541 Human_SNP_ID_614199973 m1A Human chr16 - 89894354 89894354 89894354 TCTGGGGCTGCGCGGGGGCCGTCCGGGGCTGCAAGGGGAGCTGTCCAGGGGCTGCATGAGGGCTG TCTGGGGCTGCGCGGGGGCCGTCCGGGGCTGCGAGGGGAGCTGTCCAGGGGCTGCATGAGGGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89894226..89894475 26863196 MeRIP-seq:(Medium) rs925976697 Functional Loss SNV dbSNP153 33..33 33 - - - 79542 RMVar_ID_79542 Human_SNP_ID_614199993 m1A Human chr16 + 89894388 89894367 89894388 CAGCCCCGGACGGCCCCCGCGCAGCCCCAGACAGCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC CAGCCCCGGACG_____________________GCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC GGCCCCCGCGCAGCCCCAGACA G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs887165340 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_818422,Human_RBP_ID_9374957,Human_RBP_ID_17078428,Human_RBP_ID_27838081 RMVar_hsa_circ_1394,RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_302840,RMVar_hsa_circ_122823,RMVar_hsa_circ_180787,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180790,RMVar_hsa_circ_275870,RMVar_hsa_circ_287198,RMVar_hsa_circ_342629,RMVar_hsa_circ_372753,RMVar_hsa_circ_334753,RMVar_hsa_circ_279639,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_76931,RMVar_hsa_circ_180795,RMVar_hsa_circ_180797,RMVar_hsa_circ_180798,RMVar_hsa_circ_180796,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_180800,RMVar_hsa_circ_180801 79543 RMVar_ID_79543 Human_SNP_ID_614200016 m1A Human chr16 + 89894388 89894388 89894388 CAGCCCCGGACGGCCCCCGCGCAGCCCCAGACAGCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC CAGCCCCGGACGGCCCCCGCGCAGCCCCAGACCGCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC A C TCF25 Ensembl:ENSG00000141002 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78908302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818422,Human_RBP_ID_9374957,Human_RBP_ID_17078428,Human_RBP_ID_27838081 RMVar_hsa_circ_1394,RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_302840,RMVar_hsa_circ_122823,RMVar_hsa_circ_180787,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180790,RMVar_hsa_circ_275870,RMVar_hsa_circ_287198,RMVar_hsa_circ_342629,RMVar_hsa_circ_372753,RMVar_hsa_circ_334753,RMVar_hsa_circ_279639,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_76931,RMVar_hsa_circ_180795,RMVar_hsa_circ_180797,RMVar_hsa_circ_180798,RMVar_hsa_circ_180796,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_180800,RMVar_hsa_circ_180801 79544 RMVar_ID_79544 Human_SNP_ID_614200017 m1A Human chr16 + 89894388 89894388 89894388 CAGCCCCGGACGGCCCCCGCGCAGCCCCAGACAGCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC CAGCCCCGGACGGCCCCCGCGCAGCCCCAGACGGCCCCCGGGCGGCCCTCACGCAGCCGCCGGAC A G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78908302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818422,Human_RBP_ID_9374957,Human_RBP_ID_17078428,Human_RBP_ID_27838081 RMVar_hsa_circ_1394,RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_302840,RMVar_hsa_circ_122823,RMVar_hsa_circ_180787,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180790,RMVar_hsa_circ_275870,RMVar_hsa_circ_287198,RMVar_hsa_circ_342629,RMVar_hsa_circ_372753,RMVar_hsa_circ_334753,RMVar_hsa_circ_279639,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_76931,RMVar_hsa_circ_180795,RMVar_hsa_circ_180797,RMVar_hsa_circ_180798,RMVar_hsa_circ_180796,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_180800,RMVar_hsa_circ_180801 79545 RMVar_ID_79545 Human_SNP_ID_614201391 m1A Human chr16 - 89898319 89898319 89898319 CACCCCACACACTGCTCAGCGCCCCAGTCAGCACCCGCTCCACCCCACACACTGCTTAGCGCCCC CACCCCACACACTGCTCAGCGCCCCAGTCAGCTCCCGCTCCACCCCACACACTGCTTAGCGCCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89898314..89898500 26863196 MeRIP-seq:(Medium) rs1304859432 Functional Loss SNV dbSNP153 33..33 33 - - - 79546 RMVar_ID_79546 Human_SNP_ID_614203725 m1A Human chr16 - 89904181 89904181 89904181 CTCTTTACCTTATTTCAGCATTGGGTCCAAAGAAGCGGTGACTGGAAACGCTGGCGTCGGGCCGC CTCTTTACCTTATTTCAGCATTGGGTCCAAAGCAGCGGTGACTGGAAACGCTGGCGTCGGGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89904101..89904248 26863196 MeRIP-seq:(Medium) rs767765461 Functional Loss SNV dbSNP153 33..33 33 - - - 79547 RMVar_ID_79547 Human_SNP_ID_614205098 m1A Human chr16 - 89907356 89907356 89907356 TGGGAGCTGGGAACTGGGAGGAGGGAGGTGGGAGCTGGGAGGTGGGAACTGGAAGGAGGGAGGTA TGGGAGCTGGGAACTGGGAGGAGGGAGGTGGGTGCTGGGAGGTGGGAACTGGAAGGAGGGAGGTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89907326..89907680 26863196 MeRIP-seq:(Medium) rs1299245275 Functional Loss SNV dbSNP153 33..33 33 - - - 79548 RMVar_ID_79548 Human_SNP_ID_614205640 m1A Human chr16 + 89907856 89907850 89907857 CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAATTCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTCCCACCTCACCTCCCTCCTCCCTCC_______TCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTTCCAAT C TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89907854..89908805 26863196 MeRIP-seq:(Medium) rs1427475159 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_3505953,Human_RBP_ID_5128333,Human_RBP_ID_17077778,Human_RBP_ID_18939789 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 79549 RMVar_ID_79549 Human_SNP_ID_614205642 m1A Human chr16 + 89907856 89907856 89907856 CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAATTCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTCCCACCTCACCTCCCTCCTCCCTCCTTCCACTTCCCACCTCCCAGCTCCCAGTTCCCACCTCC A C TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89907854..89908805 26863196 MeRIP-seq:(Medium) rs200953853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505953,Human_RBP_ID_5128333,Human_RBP_ID_17077778,Human_RBP_ID_18939789 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 79550 RMVar_ID_79550 Human_SNP_ID_614205643 m1A Human chr16 + 89907856 89907856 89907856 CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAATTCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAGTTCCCACCTCCCAGCTCCCAGTTCCCACCTCC A G TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89907854..89908805 26863196 MeRIP-seq:(Medium) rs200953853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505953,Human_RBP_ID_5128333,Human_RBP_ID_17077778,Human_RBP_ID_18939789 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 79551 RMVar_ID_79551 Human_SNP_ID_614205644 m1A Human chr16 + 89907856 89907856 89907856 CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAATTCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTCCCACCTCACCTCCCTCCTCCCTCCTTCCATTTCCCACCTCCCAGCTCCCAGTTCCCACCTCC A T TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89907854..89908805 26863196 MeRIP-seq:(Medium) rs200953853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3505953,Human_RBP_ID_5128333,Human_RBP_ID_17077778,Human_RBP_ID_18939789 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 79552 RMVar_ID_79552 Human_SNP_ID_614205842 m1A Human chr16 - 89908153 89908143 89908153 CGGGAGCTGGAAGGTGGGAGCTGGGAGGAGGGAGGCAGGAGGTGGCAGGGGAGGTGAGAGGAGGG CGGGAGCTGGAAGGTGGGAGCTGGGAGGAGGG__________TGGCAGGGGAGGTGAGAGGAGGG ACCTCCTGCCT A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89908091..89908214 26863196 MeRIP-seq:(Medium) rs1198201290 Functional Loss DEL dbSNP153 33..42 33 - - - 79553 RMVar_ID_79553 Human_SNP_ID_614205843 m1A Human chr16 - 89908153 89908143 89908153 CGGGAGCTGGAAGGTGGGAGCTGGGAGGAGGGAGGCAGGAGGTGGCAGGGGAGGTGAGAGGAGGG CGGGAGCTGGAAGGTGGGAGCTGGGAGGAGGG_______AGGTGGCAGGGGAGGTGAGAGGAGGG ACCTCCTGCCT ACCT - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89908091..89908214 26863196 MeRIP-seq:(Medium) rs1198201290 Functional Loss DEL dbSNP153 33..39 33 - - - 79554 RMVar_ID_79554 Human_SNP_ID_614205978 m1A Human chr16 - 89908340 89908340 89908340 GGGAGCTGGAAGATGGGAGCTGGGAGGTGGGAACTGTGAGGAAAGAAGTGGGAACTAGAAGGTGG GGGAGCTGGAAGATGGGAGCTGGGAGGTGGGAGCTGTGAGGAAAGAAGTGGGAACTAGAAGGTGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:89908326..89908574 26863196 MeRIP-seq:(Medium) rs1272898626 Functional Loss SNV dbSNP153 33..33 33 - - - 79555 RMVar_ID_79555 Human_SNP_ID_614206050 m1A Human chr16 + 89908436 89908436 89908436 TCCCAGCTCCCACCTCCCACCTTCCAGTTCCCACCTCCTTCCTCGCAGTTCCCACCTCCCAGTTC TCCCAGCTCCCACCTCCCACCTTCCAGTTCCCCCCTCCTTCCTCGCAGTTCCCACCTCCCAGTTC A C TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:89908385..89908620 26863196 MeRIP-seq:(Medium) rs1470701914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3503678,Human_RBP_ID_5097242,Human_RBP_ID_5128340,Human_RBP_ID_17077784,Human_RBP_ID_17563896,Human_RBP_ID_18939797 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 79556 RMVar_ID_79556 Human_SNP_ID_614206375 m1A Human chr16 - 89908761 89908755 89908762 TGGAAACTGGGAGGAGGGAGGCGGGAGCTGGGAGCTGGCAGGTGGGAGGCAGGAGCTGGGAGCTG TGGAAACTGGGAGGAGGGAGGCGGGAGCTGG_______CAGGTGGGAGGCAGGAGCTGGGAGCTG GCCAGCTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89908755..89908821 26863196 MeRIP-seq:(Medium) rs552528542 Functional Loss DEL dbSNP153 32..38 33 - - - 79557 RMVar_ID_79557 Human_SNP_ID_614206390 m1A Human chr16 - 89908789 89908769 89908790 TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGGAAACTGGGAGGAGGGAGGCGGGAGCTGGGAGCTG TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGG_____________________GAGCTGGGAGCTG CCCGCCTCCCTCCTCCCAGTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89907234..89908850 26863196 MeRIP-seq:(Medium) rs1262252615 Functional Loss DEL dbSNP153 32..52 33 - - - 79558 RMVar_ID_79558 Human_SNP_ID_614206396 m1A Human chr16 - 89908789 89908776 89908790 TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGGAAACTGGGAGGAGGGAGGCGGGAGCTGGGAGCTG TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGG______________GAGGCGGGAGCTGGGAGCTG CCCTCCTCCCAGTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89907234..89908850 26863196 MeRIP-seq:(Medium) rs1247604509 Functional Loss DEL dbSNP153 32..45 33 - - - 79559 RMVar_ID_79559 Human_SNP_ID_614206402 m1A Human chr16 - 89908789 89908783 89908790 TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGGAAACTGGGAGGAGGGAGGCGGGAGCTGGGAGCTG TGGGAGCTGCGAGGTGGGAGCTGGGAGGTGG_______GAGGAGGGAGGCGGGAGCTGGGAGCTG CCCAGTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89907234..89908850 26863196 MeRIP-seq:(Medium) rs201730970 Functional Loss DEL dbSNP153 32..38 33 - - - 79560 RMVar_ID_79560 Human_SNP_ID_614208389 m1A Human chr16 + 89913579 89913553 89913580 AGGCGCACGTGGCTCCCCGGGTGCCCACAGGCAGCGTGGCTCACCAGCCGGGCCCTTTTCCACTG AGGCGCA___________________________CGTGGCTCACCAGCCGGGCCCTTTTCCACTG ACGTGGCTCCCCGGGTGCCCACAGGCAG A TCF25,MC1R,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,Protein coding,lincRNA 3'UTR,exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89913531..89913642 26863196 MeRIP-seq:(Medium) rs1307710117 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_760087,Human_RBP_ID_3503681,Human_RBP_ID_5097599,Human_RBP_ID_8188380 RMVar_hsa_circ_91446,RMVar_hsa_circ_180839 79561 RMVar_ID_79561 Human_SNP_ID_614209172 m1A Human chr16 - 89914549 89914546 89914550 ACAGGCACCCACACACACAGGCGCACACACACACAAATGTGCACCCACACACACAGGCGCACACA ACAGGCACCCACACACACAGGCGCACACACA____AATGTGCACCCACACACACAGGCGCACACA TTGTG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89914290..89914638 32194978 MeRIP-seq:(Medium) rs1205908741 Functional Loss DEL dbSNP153 32..35 33 - - - 79562 RMVar_ID_79562 Human_SNP_ID_614209173 m1A Human chr16 - 89914549 89914546 89914550 ACAGGCACCCACACACACAGGCGCACACACACACAAATGTGCACCCACACACACAGGCGCACACA ACAGGCACCCACACACACAGGCGCACACACA__CAAATGTGCACCCACACACACAGGCGCACACA TTGTG TTG - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89914290..89914638 32194978 MeRIP-seq:(Medium) rs1205908741 Functional Loss DEL dbSNP153 32..33 33 - - - 79563 RMVar_ID_79563 Human_SNP_ID_614209478 m1A Human chr16 + 89914885 89914885 89914885 GCACATTTGTGTGTGTGCCTGTGTGTGGGTGCACATTTGTGTGTGTGTGCCTGTGTGTGTGTGCC GCACATTTGTGTGTGTGCCTGTGTGTGGGTGCCCATTTGTGTGTGTGTGCCTGTGTGTGTGTGCC A C MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89914835..89915034 32194978 MeRIP-seq:(Medium) rs1473479475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23708110 RMVar_hsa_circ_91446,RMVar_hsa_circ_180839 79564 RMVar_ID_79564 Human_SNP_ID_614216474 m1A Human chr16 + 89932530 89932530 89932530 GGCTTCACAAGGGAAAGGGCCTGGCTGGGGCTATGGGCCGGTGCCGACCCCCCCTCTCCCACTTT GGCTTCACAAGGGAAAGGGCCTGGCTGGGGCTTTGGGCCGGTGCCGACCCCCCCTCTCCCACTTT A T AC092143.1,TUBB3 Ensembl:ENSG00000198211,Ensembl:ENSG00000258947 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89932529..89932624 26863196 MeRIP-seq:(Medium) rs769370114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22542028,Human_RBP_ID_22653435 RMVar_hsa_circ_125474,RMVar_hsa_circ_180840 79565 RMVar_ID_79565 Human_SNP_ID_614217406 m1A Human chr16 + 89934941 89934941 89934941 GCAAGGTGCGTGAGGAGTATCCCGACCGCATCATGAACACCTTCAGCGTCGTGCCCTCACCCAAG GCAAGGTGCGTGAGGAGTATCCCGACCGCATCGTGAACACCTTCAGCGTCGTGCCCTCACCCAAG A G AC092143.1,TUBB3 Ensembl:ENSG00000198211,Ensembl:ENSG00000258947 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:89934891..89934991 32194978 MeRIP-seq:(Medium) rs971833058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1273429,Human_miRNA_ID_1273430,Human_miRNA_ID_2618089 RMVar_hsa_circ_82471,RMVar_hsa_circ_125474,RMVar_hsa_circ_180840,RMVar_hsa_circ_180845,RMVar_hsa_circ_108732,RMVar_hsa_circ_180841,RMVar_hsa_circ_99311,RMVar_hsa_circ_180843,RMVar_hsa_circ_93376,RMVar_hsa_circ_180844,RMVar_hsa_circ_180846,RMVar_hsa_circ_180848,RMVar_hsa_circ_180847,RMVar_hsa_circ_180849 79566 RMVar_ID_79566 Human_SNP_ID_614217475 m1A Human chr16 + 89935191 89935191 89935191 CACCACCTCCTTGCGCTTCCCGGGCCAGCTCAACGCTGACCTGCGCAAGCTGGCCGTCAACATGG CACCACCTCCTTGCGCTTCCCGGGCCAGCTCAGCGCTGACCTGCGCAAGCTGGCCGTCAACATGG A G AC092143.1,TUBB3 Ensembl:ENSG00000198211,Ensembl:ENSG00000258947 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:89935140..89935375 32194978 MeRIP-seq:(Medium) rs587784507 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_365 RMVar_hsa_circ_82471,RMVar_hsa_circ_125474,RMVar_hsa_circ_180840,RMVar_hsa_circ_180845,RMVar_hsa_circ_108732,RMVar_hsa_circ_180841,RMVar_hsa_circ_99311,RMVar_hsa_circ_180843,RMVar_hsa_circ_93376,RMVar_hsa_circ_180844 79567 RMVar_ID_79567 Human_SNP_ID_614217650 m1A Human chr16 + 89935757 89935757 89935757 ACCAGGACGCCACGGCCGAGGAAGAGGGCGAGATGTACGAAGACGACGAGGAGGAGTCGGAGGCC ACCAGGACGCCACGGCCGAGGAAGAGGGCGAGGTGTACGAAGACGACGAGGAGGAGTCGGAGGCC A G AC092143.1,TUBB3 Ensembl:ENSG00000198211,Ensembl:ENSG00000258947 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89935707..89935972 26863196 MeRIP-seq:(Medium) rs1284783522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12863019,Human_RBP_ID_17653148 RMVar_hsa_circ_82471,RMVar_hsa_circ_125474,RMVar_hsa_circ_180840,RMVar_hsa_circ_180845,RMVar_hsa_circ_108732,RMVar_hsa_circ_180841,RMVar_hsa_circ_99311,RMVar_hsa_circ_180843,RMVar_hsa_circ_93376,RMVar_hsa_circ_180844,RMVar_hsa_circ_180852 79568 RMVar_ID_79568 Human_SNP_ID_614217697 m1A Human chr16 + 89935831 89935831 89935831 AAGTGAAGCTGCTCGCAGCTGGAGTGAGAGGCAGGTGGCGGCCGGGGCCGAAGCCAGCAGTGTCT AAGTGAAGCTGCTCGCAGCTGGAGTGAGAGGCGGGTGGCGGCCGGGGCCGAAGCCAGCAGTGTCT A G AC092143.1,TUBB3 Ensembl:ENSG00000198211,Ensembl:ENSG00000258947 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:89935687..89935894 32194978 MeRIP-seq:(Medium) rs563540579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17653149 RMVar_hsa_circ_82471,RMVar_hsa_circ_125474,RMVar_hsa_circ_180840,RMVar_hsa_circ_180845,RMVar_hsa_circ_108732,RMVar_hsa_circ_180841,RMVar_hsa_circ_99311,RMVar_hsa_circ_180843,RMVar_hsa_circ_93376,RMVar_hsa_circ_180844,RMVar_hsa_circ_180852 79569 RMVar_ID_79569 Human_SNP_ID_614222418 m1A Human chr16 - 89949109 89948914 89949109 CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGACCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCG_________________________________ ACGGGGCCGGCGGGGACGGGGTCGGCGGGGACGGGGCTGGGAGGGACGGGGCCGGCGGGGACGGGGCCGGCGGGGACGGGGCCGGCGGGGTCGGGGCTGGGAGGGACGGGGCCGGCGGGGACGGGGTCGGCGGGGTCGGGGCTGGGAGGGACGGGGCCGGCGGGGACGGGGCCGGCGGGGACGGGGCCGGCGAGGT A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:89949101..89949257;chr16:89949107..89949936 26863196 MeRIP-seq:(Medium) rs1567776709 Functional Loss DEL dbSNP153 33..65 33 - - - 79570 RMVar_ID_79570 Human_SNP_ID_614222557 m1A Human chr16 - 89949109 89949079 89949109 CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGACCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCG______________________________TCC ACGGGGCCGGCGGGGACGGGGCCGGCGAGGT A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:89949101..89949257;chr16:89949107..89949936 26863196 MeRIP-seq:(Medium) rs1354070701 Functional Loss DEL dbSNP153 33..62 33 - - - 79571 RMVar_ID_79571 Human_SNP_ID_614222577 m1A Human chr16 - 89949109 89949094 89949109 CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGACCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCG_______________TCCCCGCCGGCCCCGTCC ACGGGGCCGGCGAGGT A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:89949101..89949257;chr16:89949107..89949936 26863196 MeRIP-seq:(Medium) rs1188549722 Functional Loss DEL dbSNP153 33..47 33 - - - 79572 RMVar_ID_79572 Human_SNP_ID_614222590 m1A Human chr16 - 89949109 89949109 89949109 CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGACCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGTCCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:89949101..89949257;chr16:89949107..89949936 26863196 MeRIP-seq:(Medium) rs1273015038 Functional Loss SNV dbSNP153 33..33 33 - - - 79573 RMVar_ID_79573 Human_SNP_ID_614222591 m1A Human chr16 - 89949109 89949109 89949109 CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGACCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC CCGCCCTCCCAGCCCCGTCCCCGCCGGCCCCGCCCTCGCCGGCCCCGTCCCCGCCGGCCCCGTCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:89949101..89949257;chr16:89949107..89949936 26863196 MeRIP-seq:(Medium) rs1273015038 Functional Loss SNV dbSNP153 33..33 33 - - - 79574 RMVar_ID_79574 Human_SNP_ID_614224203 m1A Human chr16 - 89954206 89954206 89954206 GGGCCAGGCAGGGCCAGGATGAGTCCCCAGGTACCAGGCTCACCACGGACCACCCCCTTTCCCCA GGGCCAGGCAGGGCCAGGATGAGTCCCCAGGTGCCAGGCTCACCACGGACCACCCCCTTTCCCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89954200..89955205 26863196 MeRIP-seq:(Medium) rs750082143 Functional Loss SNV dbSNP153 33..33 33 - - - 79575 RMVar_ID_79575 Human_SNP_ID_614224582 m1A Human chr16 - 89955210 89955210 89955210 AGACAGGCCGAGATCCATCACGCGTTCAGGGCAGCGGAATTCCGGCTCCCCAGGGGGCAGCTCAG AGACAGGCCGAGATCCATCACGCGTTCAGGGCGGCGGAATTCCGGCTCCCCAGGGGGCAGCTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89955119..89955225 26863196 MeRIP-seq:(Medium) rs750336491 Functional Loss SNV dbSNP153 33..33 33 - - - 79576 RMVar_ID_79576 Human_SNP_ID_614227488 m1A Human chr16 + 89963894 89963894 89963894 TCTGTGACAAGATAGAGAAGGAAGGGTGGGGAATGTGGGAAGCGTGGGGAGTGCGGGGATGCGGT TCTGTGACAAGATAGAGAAGGAAGGGTGGGGACTGTGGGAAGCGTGGGGAGTGCGGGGATGCGGT A C DEF8 Ensembl:ENSG00000140995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89963855..89963980 26863196 MeRIP-seq:(Medium) rs1234482486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5318183,Human_RBP_ID_8185562,Human_RBP_ID_9419509,Human_RBP_ID_18939809,Human_RBP_ID_21971730 RMVar_hsa_circ_128119,RMVar_hsa_circ_102234,RMVar_hsa_circ_180860,RMVar_hsa_circ_180861 79577 RMVar_ID_79577 Human_SNP_ID_614227677 m1A Human chr16 + 89964267 89964267 89964267 GCATGCCGGCCGCCTGGGCTGCTCGCTCACCGAGATCCACACGCTCTTCGCCAAGCACATCAAGC GCATGCCGGCCGCCTGGGCTGCTCGCTCACCGCGATCCACACGCTCTTCGCCAAGCACATCAAGC A C DEF8 Ensembl:ENSG00000140995 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89964188..89964289 32194978 MeRIP-seq:(Medium) rs774383955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27447740 Human_Splice_Rec_1754756,Human_Splice_Rec_1754757,Human_Splice_Rec_1754796,Human_Splice_Rec_1754797,Human_Splice_Rec_1754870,Human_Splice_Rec_1754871,Human_Splice_Rec_1754904,Human_Splice_Rec_1754905,Human_Splice_Rec_1754996,Human_Splice_Rec_1754997,Human_Splice_Rec_1755020,Human_Splice_Rec_1755021,Human_Splice_Rec_1755044,Human_Splice_Rec_1755045,Human_Splice_Rec_1755068,Human_Splice_Rec_1755072,Human_Splice_Rec_1755073,Human_Splice_Rec_1755077 RMVar_hsa_circ_128119,RMVar_hsa_circ_102234,RMVar_hsa_circ_180860,RMVar_hsa_circ_180861 79578 RMVar_ID_79578 Human_SNP_ID_441964743 m1A Human chr10 + 90906339 90906339 90906339 GTGGGAAGAAGAGTCTTCCAGGGAGCTGGCACAGTATGTGAAAACAGTAAAGCAAGTGCCTGGAT GTGGGAAGAAGAGTCTTCCAGGGAGCTGGCACGGTATGTGAAAACAGTAAAGCAAGTGCCTGGAT A G RPP30 Ensembl:ENSG00000148688 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:90906288..90906383 26863196 MeRIP-seq:(Medium) rs1282623928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_384828 79579 RMVar_ID_79579 Human_SNP_ID_441967085 m1A Human chr10 - 90915840 90915840 90915840 CACAGCGCTGCATGTGGCGGTGAGGACTGGCCACTATGAGTGCGCGGAGCATCTTATCGCCTGTG CACAGCGCTGCATGTGGCGGTGAGGACTGGCCGCTATGAGTGCGCGGAGCATCTTATCGCCTGTG T C ANKRD1 Ensembl:ENSG00000148677 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:90915790..90917741 32194978 MeRIP-seq:(Medium) rs1486211072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1159480,Human_Splice_Rec_1159481 RMVar_hsa_circ_91576,RMVar_hsa_circ_144839,RMVar_hsa_circ_114873,RMVar_hsa_circ_144841,RMVar_hsa_circ_76031,RMVar_hsa_circ_89663,RMVar_hsa_circ_144842,RMVar_hsa_circ_144840 79580 RMVar_ID_79580 Human_SNP_ID_442027711 m1A Human chr10 + 91162960 91162960 91162960 GGCCGGCCCAGCCCCCGCCCCGCGCCGCTCGCACCCCCGCTGCCCCGCCCCGCCCCCGCCGGCGC GGCCGGCCCAGCCCCCGCCCCGCGCCGCTCGCCCCCCCGCTGCCCCGCCCCGCCCCCGCCGGCGC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:91162932..91163101 26863196 MeRIP-seq:(Medium) rs1460161593 Functional Loss SNV dbSNP153 33..33 33 - - - 79581 RMVar_ID_79581 Human_SNP_ID_442028990 m1A Human chr10 - 91168166 91168166 91168166 TGAACTTTCTGACAGGTTCACCATCCCCCTCCATAAGGATGCCCCAAATCTTTCTGTATTTTTAA TGAACTTTCTGACAGGTTCACCATCCCCCTCCCTAAGGATGCCCCAAATCTTTCTGTATTTTTAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:91168161..91168429 26863196 MeRIP-seq:(Medium) rs1285904215 Functional Loss SNV dbSNP153 33..33 33 - - - 79582 RMVar_ID_79582 Human_SNP_ID_442036722 m1A Human chr10 - 91200975 91200975 91200975 TCCATTTGCCTCTTGAATCTTGTGCTTGCCCAAGCTCTGACCATTCTCCCACCTGACCCTCCCCC TCCATTTGCCTCTTGAATCTTGTGCTTGCCCAGGCTCTGACCATTCTCCCACCTGACCCTCCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:91200973..91201056 26863196 MeRIP-seq:(Medium) rs560447159 Functional Loss SNV dbSNP153 33..33 33 - - - 79583 RMVar_ID_79583 Human_SNP_ID_442036723 m1A Human chr10 - 91200975 91200975 91200975 TCCATTTGCCTCTTGAATCTTGTGCTTGCCCAAGCTCTGACCATTCTCCCACCTGACCCTCCCCC TCCATTTGCCTCTTGAATCTTGTGCTTGCCCACGCTCTGACCATTCTCCCACCTGACCCTCCCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:91200973..91201056 26863196 MeRIP-seq:(Medium) rs560447159 Functional Loss SNV dbSNP153 33..33 33 - - - 79584 RMVar_ID_79584 Human_SNP_ID_442086701 m1A Human chr10 + 91410472 91410472 91410472 TGAGTGAGGCGGTTCGGGTACCCTCGCCCGCCACTCCGCTGGTGGTGGCGGCGCCCGCGCCTGAG TGAGTGAGGCGGTTCGGGTACCCTCGCCCGCCTCTCCGCTGGTGGTGGCGGCGCCCGCGCCTGAG A T HECTD2 Ensembl:ENSG00000165338 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:91410402..91410548 26863196 MeRIP-seq:(Medium) rs1380642467 Functional Loss SNV dbSNP153 33..33 33 - - - 79585 RMVar_ID_79585 Human_SNP_ID_442086738 m1A Human chr10 - 91410501 91410501 91410501 TCGCGCTCTGACTCCTTCCCTTTCCTCTCCTCAGGCGCGGGCGCCGCCACCACCAGCGGAGTGGC TCGCGCTCTGACTCCTTCCCTTTCCTCTCCTCTGGCGCGGGCGCCGCCACCACCAGCGGAGTGGC T A lnc-PPP1R3C-3,HECTD2-AS1,HECTD2-AS1:2,HECTD2-AS1:3,HECTD2-AS1:4,HECTD2-AS1:5,HECTD2-AS1:6,HECTD2-AS1:7,HECTD2-AS1:8 RNACentral:URS00008BEC10,RNACentral:URS00008BFD10,RNACentral:URS0000D57E38,RNACentral:URS0000D5BB08,RNACentral:URS000075B789,RNACentral:URS00009B739A,RNACentral:URS0000D5CD85,RNACentral:URS00008B9A59,RNACentral:URS0000D5B1EA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:91410110..91410622;chr10:91410096..91410635 26863196 MeRIP-seq:(Medium) rs1201288073 Functional Loss SNV dbSNP153 33..33 33 - - - 79586 RMVar_ID_79586 Human_SNP_ID_442086749 m1A Human chr10 + 91410513 91410513 91410513 GTGGTGGCGGCGCCCGCGCCTGAGGAGAGGAAAGGGAAGGAGTCAGAGCGCGAGAAGCTGCCGCC GTGGTGGCGGCGCCCGCGCCTGAGGAGAGGAAGGGGAAGGAGTCAGAGCGCGAGAAGCTGCCGCC A G HECTD2 Ensembl:ENSG00000165338 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:91410387..91425297 26863196 MeRIP-seq:(Medium) rs1474940542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1159569,Human_Splice_Rec_1159611,Human_Splice_Rec_1159619 79587 RMVar_ID_79587 Human_SNP_ID_442128334 m1A Human chr10 + 91589833 91589833 91589833 AGTGAGGAGGTGAGAGGGACAGGGGACAGAGTAAGGAGTGGCCTGGTGGGCATGGGGTTGACTGA AGTGAGGAGGTGAGAGGGACAGGGGACAGAGTGAGGAGTGGCCTGGTGGGCATGGGGTTGACTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:91589705..91589920 26863196 MeRIP-seq:(Medium) rs72821230 Functional Loss SNV dbSNP153 33..33 33 - - - 79588 RMVar_ID_79588 Human_SNP_ID_442203908 m1A Human chr10 - 91908476 91908476 91908476 CGCACGCCCCACCGTCGCGGGATTCGCGGGGGAGTCCAAGCCCCGGGCCCGGAACCGGGGGCGGA CGCACGCCCCACCGTCGCGGGATTCGCGGGGGTGTCCAAGCCCCGGGCCCGGAACCGGGGGCGGA T A FGFBP3 Ensembl:ENSG00000174721 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:91908395..91908684 26863410 MeRIP-seq:(Medium) rs1564642123 Functional Loss SNV dbSNP153 33..33 33 - - - 79589 RMVar_ID_79589 Human_SNP_ID_442207719 m1A Human chr10 - 91923867 91923867 91923867 CGTCCCCGCGGCGGCCGGTAAGCAGGGGTCCAAGACGGTAGCGGAGGCGGCAGTCCTCCGACCCG CGTCCCCGCGGCGGCCGGTAAGCAGGGGTCCAGGACGGTAGCGGAGGCGGCAGTCCTCCGACCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:91923817..91923972 26863196 MeRIP-seq:(Medium) rs1029387067 Functional Loss SNV dbSNP153 33..33 33 - - - 79590 RMVar_ID_79590 Human_SNP_ID_442207725 m1A Human chr10 - 91923876 91923876 91923876 ACCCGAGCTCGTCCCCGCGGCGGCCGGTAAGCAGGGGTCCAAGACGGTAGCGGAGGCGGCAGTCC ACCCGAGCTCGTCCCCGCGGCGGCCGGTAAGCCGGGGTCCAAGACGGTAGCGGAGGCGGCAGTCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:91923826..91924025 26863196 MeRIP-seq:(Medium) rs1036673632 Functional Loss SNV dbSNP153 33..33 33 - - - 79591 RMVar_ID_79591 Human_SNP_ID_442215286 m1A Human chr10 + 91952756 91952756 91952756 AGGAGAGAAAAAAGAGAGAGTATGAAGAGGCCAGAATACAGCAACACCCTGAAAGGAACAGAAGG AGGAGAGAAAAAAGAGAGAGTATGAAGAGGCCGGAATACAGCAACACCCTGAAAGGAACAGAAGG A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:91952713..91952865;chr10:91952730..91952923 26863196 MeRIP-seq:(Medium) rs1273732001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23476474 RMVar_hsa_circ_5278,RMVar_hsa_circ_24397,RMVar_hsa_circ_341436,RMVar_hsa_circ_107889,RMVar_hsa_circ_144903,RMVar_hsa_circ_344820,RMVar_hsa_circ_321032,RMVar_hsa_circ_340817,RMVar_hsa_circ_303323,RMVar_hsa_circ_276735,RMVar_hsa_circ_51384,RMVar_hsa_circ_144907,RMVar_hsa_circ_144909,RMVar_hsa_circ_144911,RMVar_hsa_circ_21919,RMVar_hsa_circ_144910,RMVar_hsa_circ_144908,RMVar_hsa_circ_144906,RMVar_hsa_circ_311052,RMVar_hsa_circ_333819,RMVar_hsa_circ_378426,RMVar_hsa_circ_341483,RMVar_hsa_circ_327701,RMVar_hsa_circ_23172,RMVar_hsa_circ_273806,RMVar_hsa_circ_20046,RMVar_hsa_circ_144917,RMVar_hsa_circ_280705,RMVar_hsa_circ_319166,RMVar_hsa_circ_144913,RMVar_hsa_circ_144914,RMVar_hsa_circ_144915,RMVar_hsa_circ_322173,RMVar_hsa_circ_144912,RMVar_hsa_circ_373691,RMVar_hsa_circ_321100,RMVar_hsa_circ_313433,RMVar_hsa_circ_315723,RMVar_hsa_circ_298362,RMVar_hsa_circ_71183,RMVar_hsa_circ_101688,RMVar_hsa_circ_274430,RMVar_hsa_circ_74088,RMVar_hsa_circ_144921,RMVar_hsa_circ_23870,RMVar_hsa_circ_25348,RMVar_hsa_circ_144923,RMVar_hsa_circ_144924,RMVar_hsa_circ_144922,RMVar_hsa_circ_144919,RMVar_hsa_circ_144920,RMVar_hsa_circ_144918,RMVar_hsa_circ_144916 79592 RMVar_ID_79592 Human_SNP_ID_442217226 m1A Human chr10 + 91960016 91960016 91960016 GCACCAGTTCGTGAAACTTGTGCTCAAACATTAGGTGTGGTTTTAAAACACATGAACGAAACAGG GCACCAGTTCGTGAAACTTGTGCTCAAACATTGGGTGTGGTTTTAAAACACATGAACGAAACAGG A G BTAF1 Ensembl:ENSG00000095564 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:91959885..91960015 32194978 MeRIP-seq:(Medium) rs756541425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26450,Human_RBP_ID_1772697,Human_RBP_ID_18600264,Human_RBP_ID_24556899,Human_RBP_ID_24852981 Human_Splice_Rec_1159770,Human_Splice_Rec_1159842,Human_Splice_Rec_1159904 RMVar_hsa_circ_5278,RMVar_hsa_circ_341436,RMVar_hsa_circ_107889,RMVar_hsa_circ_144903,RMVar_hsa_circ_344820,RMVar_hsa_circ_340817,RMVar_hsa_circ_303323,RMVar_hsa_circ_51384,RMVar_hsa_circ_144909,RMVar_hsa_circ_144911,RMVar_hsa_circ_21919,RMVar_hsa_circ_144910,RMVar_hsa_circ_144908,RMVar_hsa_circ_311052,RMVar_hsa_circ_378426,RMVar_hsa_circ_341483,RMVar_hsa_circ_327701,RMVar_hsa_circ_58197,RMVar_hsa_circ_319166,RMVar_hsa_circ_144913,RMVar_hsa_circ_322173,RMVar_hsa_circ_144912,RMVar_hsa_circ_373691,RMVar_hsa_circ_321100,RMVar_hsa_circ_298362,RMVar_hsa_circ_71183,RMVar_hsa_circ_101688,RMVar_hsa_circ_274430,RMVar_hsa_circ_74088,RMVar_hsa_circ_144921,RMVar_hsa_circ_23870,RMVar_hsa_circ_25348,RMVar_hsa_circ_144923,RMVar_hsa_circ_144924,RMVar_hsa_circ_144922,RMVar_hsa_circ_144919,RMVar_hsa_circ_144920,RMVar_hsa_circ_64826,RMVar_hsa_circ_91375,RMVar_hsa_circ_73984,RMVar_hsa_circ_302054,RMVar_hsa_circ_34351,RMVar_hsa_circ_144925,RMVar_hsa_circ_348646,RMVar_hsa_circ_295890,RMVar_hsa_circ_61368,RMVar_hsa_circ_33699,RMVar_hsa_circ_307732,RMVar_hsa_circ_144926,RMVar_hsa_circ_144927,RMVar_hsa_circ_314365,RMVar_hsa_circ_316418,RMVar_hsa_circ_51886,RMVar_hsa_circ_48734,RMVar_hsa_circ_144928,RMVar_hsa_circ_144929,RMVar_hsa_circ_144930,RMVar_hsa_circ_123200,RMVar_hsa_circ_373492,RMVar_hsa_circ_144933,RMVar_hsa_circ_144931,RMVar_hsa_circ_144932,RMVar_hsa_circ_109748 79593 RMVar_ID_79593 Human_SNP_ID_442252502 m1A Human chr10 - 92105482 92105482 92105482 AATGTGGAGTTGGCCAAGAGAAGGGTGGAAGTATAGGGAATAAAAATTTCAGAGAAAGGCAAAAA AATGTGGAGTTGGCCAAGAGAAGGGTGGAAGTGTAGGGAATAAAAATTTCAGAGAAAGGCAAAAA T C CPEB3 Ensembl:ENSG00000107864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:92105393..92105517 26863196 MeRIP-seq:(Medium) rs914689203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39990,RMVar_hsa_circ_144960,RMVar_hsa_circ_85070,RMVar_hsa_circ_310304,RMVar_hsa_circ_310602,RMVar_hsa_circ_322768,RMVar_hsa_circ_295468,RMVar_hsa_circ_144961,RMVar_hsa_circ_144963,RMVar_hsa_circ_144965,RMVar_hsa_circ_144966,RMVar_hsa_circ_144964,RMVar_hsa_circ_144962,RMVar_hsa_circ_144970,RMVar_hsa_circ_302330,RMVar_hsa_circ_323511,RMVar_hsa_circ_52524,RMVar_hsa_circ_144969 79594 RMVar_ID_79594 Human_SNP_ID_442296086 m1A Human chr10 + 92291227 92291227 92291227 AGCAACTCGGCGCCCGCGGTCCATGGACCGGAACCTCGGGCCGACGGACGGGAACCCGGGCCGCG AGCAACTCGGCGCCCGCGGTCCATGGACCGGAGCCTCGGGCCGACGGACGGGAACCCGGGCCGCG A G MARCHF5 Ensembl:ENSG00000198060 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:92291176..92291400 26863196 MeRIP-seq:(Medium) rs538400700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226001,Human_RBP_ID_4132174 79595 RMVar_ID_79595 Human_SNP_ID_442311126 m1A Human chr10 + 92351474 92351474 92351474 TTATCTTAGCATGGTAAACCTGGGTTTTGTTCATATTTTCTCCAGACAGAAATGCAAAGATCAAA TTATCTTAGCATGGTAAACCTGGGTTTTGTTCGTATTTTCTCCAGACAGAAATGCAAAGATCAAA A G MARCHF5 Ensembl:ENSG00000198060 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:92351425..92351515 32194978 MeRIP-seq:(Medium) rs1404514276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385166,Human_RBP_ID_1451742,Human_RBP_ID_2238109,Human_RBP_ID_11461513,Human_RBP_ID_18245294,Human_RBP_ID_21882329,Human_RBP_ID_22378799,Human_RBP_ID_23476849,Human_RBP_ID_26600990 79596 RMVar_ID_79596 Human_SNP_ID_442371933 m1A Human chr10 - 92593181 92593181 92593181 CGGTACTCTGGCCGTGGCGTTTGTCCCGCGCCAGTCGGAGCCGCCAAATCACTAATCTCGTCTCC CGGTACTCTGGCCGTGGCGTTTGTCCCGCGCCTGTCGGAGCCGCCAAATCACTAATCTCGTCTCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:92593136..92593287 26863196 MeRIP-seq:(Medium) rs180781687 Functional Loss SNV dbSNP153 33..33 33 - - - 79597 RMVar_ID_79597 Human_SNP_ID_442371968 m1A Human chr10 - 92593301 92593301 92593301 GCGCTGTGAGGGGCGGAGGGGCTTGGCGGCCGACAGGGGCCGGAGTCTCCCTGGTCCCTCTCGGG GCGCTGTGAGGGGCGGAGGGGCTTGGCGGCCGGCAGGGGCCGGAGTCTCCCTGGTCCCTCTCGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:92593276..92593300 26863196 MeRIP-seq:(Medium) rs1279062404 Functional Loss SNV dbSNP153 33..33 33 - - - 79598 RMVar_ID_79598 Human_SNP_ID_442371989 m1A Human chr10 + 92593336 92593336 92593336 GCCGCCAAGCCCCTCCGCCCCTCACAGCGCCCAGGTCCGCGGCCGGGCCTTGATTTTTTGGCGGG GCCGCCAAGCCCCTCCGCCCCTCACAGCGCCCGGGTCCGCGGCCGGGCCTTGATTTTTTGGCGGG A G KIF11 Ensembl:ENSG00000138160 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:92593326..92593350 26863196 MeRIP-seq:(Medium) rs1276590257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136424,Human_RBP_ID_8765691 RMVar_hsa_circ_145011,RMVar_hsa_circ_113828 79599 RMVar_ID_79599 Human_SNP_ID_442379559 m1A Human chr10 + 92622823 92622823 92622823 TTCCATAGGCTGTACAGGAGGCATGGCTGGGGAGGCTTCAGGAAACTTACAATCCTGGTAGAAGA TTCCATAGGCTGTACAGGAGGCATGGCTGGGGGGGCTTCAGGAAACTTACAATCCTGGTAGAAGA A G KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:92622818..92622883 26863196 MeRIP-seq:(Medium) rs1396034814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67654,RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_74358,RMVar_hsa_circ_145018,RMVar_hsa_circ_50938,RMVar_hsa_circ_345773,RMVar_hsa_circ_348727,RMVar_hsa_circ_356062,RMVar_hsa_circ_57231 79600 RMVar_ID_79600 Human_SNP_ID_442396161 m1A Human chr10 + 92690122 92690122 92690122 AGGACATCCTGGGCCGCGGGCCCGCCGCGCCCACGCCCGCCCCCACGCTGCCGTCCCCCAACTCC AGGACATCCTGGGCCGCGGGCCCGCCGCGCCCGCGCCCGCCCCCACGCTGCCGTCCCCCAACTCC A G HHEX Ensembl:ENSG00000152804 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:92690078..92690260 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4132468,Human_RBP_ID_9320657,Human_RBP_ID_26802823 Human_miRNA_ID_2386803,Human_miRNA_ID_2388280,Human_miRNA_ID_2399429,Human_miRNA_ID_3030483 RMVar_hsa_circ_120779,RMVar_hsa_circ_67063,RMVar_hsa_circ_145030 79601 RMVar_ID_79601 Human_SNP_ID_442396194 m1A Human chr10 - 92690179 92690179 92690179 GATCGGCGTGGGCTCGTACACCGGGGTCCGGTAGGGGGACACGAGGCTGGTGAAGGAGGAGTTGG GATCGGCGTGGGCTCGTACACCGGGGTCCGGTGGGGGGACACGAGGCTGGTGAAGGAGGAGTTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:92690043..92690311 26863196 MeRIP-seq:(Medium) rs1332097827 Functional Loss SNV dbSNP153 33..33 33 - - - 79602 RMVar_ID_79602 Human_SNP_ID_442396207 m1A Human chr10 - 92690194 92690194 92690194 CGAGAAGGCTGGATGGATCGGCGTGGGCTCGTACACCGGGGTCCGGTAGGGGGACACGAGGCTGG CGAGAAGGCTGGATGGATCGGCGTGGGCTCGTCCACCGGGGTCCGGTAGGGGGACACGAGGCTGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:92689985..92690347 26863196 MeRIP-seq:(Medium) rs1204238532 Functional Loss SNV dbSNP153 33..33 33 - - - 79603 RMVar_ID_79603 Human_SNP_ID_442396296 m1A Human chr10 + 92690386 92690386 92690386 CGGCCGGGCGAGGGTGGGGGCGAGGAAGCGCCACCCGGCAGGTGGCAGCGCCCGGGAGGCCGAGG CGGCCGGGCGAGGGTGGGGGCGAGGAAGCGCCCCCCGGCAGGTGGCAGCGCCCGGGAGGCCGAGG A C HHEX Ensembl:ENSG00000152804 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:92690377..92690518 26863196 MeRIP-seq:(Medium) rs1335682853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259277,Human_RBP_ID_863992,Human_RBP_ID_5340013,Human_RBP_ID_5643353,Human_RBP_ID_8725039,Human_RBP_ID_9320659,Human_RBP_ID_9361415,Human_RBP_ID_9413147,Human_RBP_ID_17668583,Human_RBP_ID_19045576,Human_RBP_ID_22030318,Human_RBP_ID_22640322,Human_RBP_ID_23255698,Human_RBP_ID_26774902,Human_RBP_ID_27836047 RMVar_hsa_circ_120779,RMVar_hsa_circ_67063,RMVar_hsa_circ_145030 79604 RMVar_ID_79604 Human_SNP_ID_442433376 m1A Human chr10 + 92848552 92848552 92848552 AGCTTCCAGCCAAAATGGCGGAGAACAGCGAGAGTCTGGGCACCGTCCCCGAGCACGAGCGGATC AGCTTCCAGCCAAAATGGCGGAGAACAGCGAGCGTCTGGGCACCGTCCCCGAGCACGAGCGGATC A C EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:92848501..92893376 26863196 MeRIP-seq:(Medium) rs779861174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4144566,Human_RBP_ID_18416150 Human_Splice_Rec_1160415,Human_Splice_Rec_1160449,Human_Splice_Rec_1160457 RMVar_hsa_circ_58509,RMVar_hsa_circ_61323 79605 RMVar_ID_79605 Human_SNP_ID_442433400 m1A Human chr10 + 92848594 92848594 92848594 CCGTCCCCGAGCACGAGCGGATCTTGCAGGAGATCGAGAGCACCGACACCGCCTGTGTGGGGCCC CCGTCCCCGAGCACGAGCGGATCTTGCAGGAGCTCGAGAGCACCGACACCGCCTGTGTGGGGCCC A C EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:92848544..92848630 26863196 MeRIP-seq:(Medium) rs776059707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4132498,Human_RBP_ID_18416309,Human_RBP_ID_23477224 Human_Splice_Rec_1160415,Human_Splice_Rec_1160449,Human_Splice_Rec_1160457 RMVar_hsa_circ_58509,RMVar_hsa_circ_61323 79606 RMVar_ID_79606 Human_SNP_ID_442433401 m1A Human chr10 + 92848594 92848594 92848594 CCGTCCCCGAGCACGAGCGGATCTTGCAGGAGATCGAGAGCACCGACACCGCCTGTGTGGGGCCC CCGTCCCCGAGCACGAGCGGATCTTGCAGGAGGTCGAGAGCACCGACACCGCCTGTGTGGGGCCC A G EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:92848544..92848630 26863196 MeRIP-seq:(Medium) rs776059707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4132498,Human_RBP_ID_18416309,Human_RBP_ID_23477224 Human_Splice_Rec_1160415,Human_Splice_Rec_1160449,Human_Splice_Rec_1160457 RMVar_hsa_circ_58509,RMVar_hsa_circ_61323 79607 RMVar_ID_79607 Human_SNP_ID_442433402 m1A Human chr10 - 92848595 92848595 92848595 TGGGCCCCACACAGGCGGTGTCGGTGCTCTCGATCTCCTGCAAGATCCGCTCGTGCTCGGGGACG TGGGCCCCACACAGGCGGTGTCGGTGCTCTCGGTCTCCTGCAAGATCCGCTCGTGCTCGGGGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:92848545..92848666 26863196 MeRIP-seq:(Medium) rs1345601307 Functional Loss SNV dbSNP153 33..33 33 - - - 79608 RMVar_ID_79608 Human_SNP_ID_442550861 m1A Human chr10 - 93333825 93333825 93333825 ACAGTTTCGGGAATTACCTGACAGCGTCCCACAGGAATGCACGGTTAGGATTTACATTGTTCGAG ACAGTTTCGGGAATTACCTGACAGCGTCCCACGGGAATGCACGGTTAGGATTTACATTGTTCGAG T C MYOF Ensembl:ENSG00000138119 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:93333751..93333925 32194978 MeRIP-seq:(Medium) rs1251625590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1160646,Human_Splice_Rec_1160647,Human_Splice_Rec_1160750,Human_Splice_Rec_1160751,Human_Splice_Rec_1160854,Human_Splice_Rec_1160855 RMVar_hsa_circ_88542,RMVar_hsa_circ_106860,RMVar_hsa_circ_89315,RMVar_hsa_circ_145082,RMVar_hsa_circ_125510,RMVar_hsa_circ_145084,RMVar_hsa_circ_145085,RMVar_hsa_circ_78186,RMVar_hsa_circ_145088,RMVar_hsa_circ_81269,RMVar_hsa_circ_122497,RMVar_hsa_circ_145089,RMVar_hsa_circ_145090,RMVar_hsa_circ_67150,RMVar_hsa_circ_44737,RMVar_hsa_circ_77245,RMVar_hsa_circ_145091,RMVar_hsa_circ_100823,RMVar_hsa_circ_145093,RMVar_hsa_circ_98122,RMVar_hsa_circ_145094,RMVar_hsa_circ_145095 79609 RMVar_ID_79609 Human_SNP_ID_442567517 m1A Human chr10 - 93398165 93398165 93398165 GGAAGGCCTGCCCATGTGGCTGCGGTAGAGCCAGCAAGCGGGGAAAACTAGGAGGTCAGTGAGAA GGAAGGCCTGCCCATGTGGCTGCGGTAGAGCCCGCAAGCGGGGAAAACTAGGAGGTCAGTGAGAA T G MYOF Ensembl:ENSG00000138119 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:93398154..93398246 26863196 MeRIP-seq:(Medium) rs887943260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88542,RMVar_hsa_circ_106860,RMVar_hsa_circ_89315,RMVar_hsa_circ_145082,RMVar_hsa_circ_145085,RMVar_hsa_circ_145088,RMVar_hsa_circ_100823,RMVar_hsa_circ_145094,RMVar_hsa_circ_83287,RMVar_hsa_circ_145099,RMVar_hsa_circ_27829,RMVar_hsa_circ_116801,RMVar_hsa_circ_145109,RMVar_hsa_circ_23601,RMVar_hsa_circ_332728,RMVar_hsa_circ_145111,RMVar_hsa_circ_16802,RMVar_hsa_circ_145112,RMVar_hsa_circ_81159 79610 RMVar_ID_79610 Human_SNP_ID_442588749 m1A Human chr10 - 93482241 93482240 93482242 CAGGGCGGTGCGACCCGGAGCTCCAGCGCCCTAGTCTCCACTTCGTTTGCTGAAACTTGCTTTCT CAGGGCGGTGCGACCCGGAGCTCCAGCGCCC__GTCTCCACTTCGTTTGCTGAAACTTGCTTTCT CTA C MYOF Ensembl:ENSG00000138119 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:93482190..93482263 26863196 MeRIP-seq:(Medium) rs775615262 Functional Loss DEL dbSNP153 32..33 33 - - - Human_miRNA_ID_2882317 RMVar_hsa_circ_106860,RMVar_hsa_circ_145082,RMVar_hsa_circ_111543,RMVar_hsa_circ_145117 79611 RMVar_ID_79611 Human_SNP_ID_442588750 m1A Human chr10 - 93482241 93482241 93482241 CAGGGCGGTGCGACCCGGAGCTCCAGCGCCCTAGTCTCCACTTCGTTTGCTGAAACTTGCTTTCT CAGGGCGGTGCGACCCGGAGCTCCAGCGCCCTGGTCTCCACTTCGTTTGCTGAAACTTGCTTTCT T C MYOF Ensembl:ENSG00000138119 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:93482190..93482263 26863196 MeRIP-seq:(Medium) rs1346576318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2882317 RMVar_hsa_circ_106860,RMVar_hsa_circ_145082,RMVar_hsa_circ_111543,RMVar_hsa_circ_145117 79612 RMVar_ID_79612 Human_SNP_ID_442592584 m1A Human chr10 + 93496701 93496701 93496701 CGCTTCGCTTCAGCTGCTAGCTGGCCCAAGGGAGGCGACCGCGGAGGGTGGCGAGGGGCGGCCAG CGCTTCGCTTCAGCTGCTAGCTGGCCCAAGGGTGGCGACCGCGGAGGGTGGCGAGGGGCGGCCAG A T CEP55 Ensembl:ENSG00000138180 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:93496650..93496784;chr10:93496654..93496772 26863196 MeRIP-seq:(Medium) rs1010461929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136937,Human_RBP_ID_9360576,Human_RBP_ID_27802244 79613 RMVar_ID_79613 Human_SNP_ID_442592602 m1A Human chr10 - 93496760 93496760 93496760 TGCCCACTGACCTGCCCTCCCTGGCGGTCCGGACCGGCCCGGCCCCGGGGCTGCGGGTCCTGGCC TGCCCACTGACCTGCCCTCCCTGGCGGTCCGGCCCGGCCCGGCCCCGGGGCTGCGGGTCCTGGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:93496659..93496800 26863196 MeRIP-seq:(Medium) rs1000112075 Functional Loss SNV dbSNP153 33..33 33 - - - 79614 RMVar_ID_79614 Human_SNP_ID_442642641 m1A Human chr10 + 93698190 93698186 93698191 AACCTTCTATTTCTTGCTTCTTCCCTGTTAAAACAAATTTTTTTAAGAAAATTCAAAATGTTTAT AACCTTCTATTTCTTGCTTCTTCCCTGTT_____AAATTTTTTTAAGAAAATTCAAAATGTTTAT TAAAAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:93698188..93698274 26863196 MeRIP-seq:(Medium) rs1367966670 Functional Loss DEL dbSNP153 30..34 33 - - - 79615 RMVar_ID_79615 Human_SNP_ID_442643734 m1A Human chr10 - 93702461 93702461 93702461 GCGCACGGGACCTGTGCTGCAGCGGCTCTCTCAGGCCGTGGGTCGTCGCTGCAGCTGCCGGGAAA GCGCACGGGACCTGTGCTGCAGCGGCTCTCTCGGGCCGTGGGTCGTCGCTGCAGCTGCCGGGAAA T C FRA10AC1 Ensembl:ENSG00000148690 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:93702445..93702527 26863410 MeRIP-seq:(Medium) rs1564824880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4132636,Human_RBP_ID_6017701,Human_RBP_ID_11467167,Human_RBP_ID_17105090,Human_RBP_ID_18970962,Human_RBP_ID_24862270 Human_Splice_Rec_1161055 79616 RMVar_ID_79616 Human_SNP_ID_442643735 m1A Human chr10 + 93702465 93702461 93702465 CCGGCAGCTGCAGCGACGACCCACGGCCTGAGAGAGCCGCTGCAGCACAGGTCCCGTGCGCCCTG CCGGCAGCTGCAGCGACGACCCACGGCCT____GAGCCGCTGCAGCACAGGTCCCGTGCGCCCTG TGAGA T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:93702401..93702525 26863410 MeRIP-seq:(Medium) rs1291049176 Functional Loss DEL dbSNP153 30..33 33 - - - 79617 RMVar_ID_79617 Human_SNP_ID_442643736 m1A Human chr10 + 93702465 93702461 93702465 CCGGCAGCTGCAGCGACGACCCACGGCCTGAGAGAGCCGCTGCAGCACAGGTCCCGTGCGCCCTG CCGGCAGCTGCAGCGACGACCCACGGCCTGA__GAGCCGCTGCAGCACAGGTCCCGTGCGCCCTG TGAGA TGA - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:93702401..93702525 26863410 MeRIP-seq:(Medium) rs1291049176 Functional Loss DEL dbSNP153 32..33 33 - - - 79618 RMVar_ID_79618 Human_SNP_ID_442797240 m1A Human chr10 - 94362795 94362795 94362795 AAGTGTCCTCAAAAGCCCGGTCGCCGCGGCCTAGGGCCCCTTCGGGTGATAGAGTCACTGCCTGA AAGTGTCCTCAAAAGCCCGGTCGCCGCGGCCTCGGGCCCCTTCGGGTGATAGAGTCACTGCCTGA T G NOC3L Ensembl:ENSG00000173145 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:94362792..94362922 26863196 MeRIP-seq:(Medium) rs752932699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19046938 79619 RMVar_ID_79619 Human_SNP_ID_442807299 m1A Human chr10 + 94402762 94402762 94402762 TGGCGGAGGCGTCGGCGCTGTGGAGCCGCCGGAGGAGGCTGACGAGGAGGAGGAGGCTGACGAGG TGGCGGAGGCGTCGGCGCTGTGGAGCCGCCGGCGGAGGCTGACGAGGAGGAGGAGGCTGACGAGG A C TBC1D12 Ensembl:ENSG00000108239 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:94402538..94403498;chr10:94402577..94403018;chr10:94402553..94403398 26863196 MeRIP-seq:(Medium) rs1197749473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4132915 79620 RMVar_ID_79620 Human_SNP_ID_442807477 m1A Human chr10 - 94403100 94403100 94403100 GCGAAGGCGGCCGTAGGGGCGGCGGCGGCGCGACTCCCGGCCGCCGGCGCGCGCCAGCCCGCGAG GCGAAGGCGGCCGTAGGGGCGGCGGCGGCGCGCCTCCCGGCCGCCGGCGCGCGCCAGCCCGCGAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:94403051..94403151 26863196 MeRIP-seq:(Medium) rs1347051634 Functional Loss SNV dbSNP153 33..33 33 - - - 79621 RMVar_ID_79621 Human_SNP_ID_442812668 m1A Human chr10 - 94424849 94424849 94424849 CAGACATGCCACAGTGACCTTCTAGAACTCTTACCAGTTTACTTTAAACCCATTAATTAGAATTC CAGACATGCCACAGTGACCTTCTAGAACTCTTGCCAGTTTACTTTAAACCCATTAATTAGAATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:94424836..94425020 26863196 MeRIP-seq:(Medium) rs956366470 Functional Loss SNV dbSNP153 33..33 33 - - - 79622 RMVar_ID_79622 Human_SNP_ID_442842036 m1A Human chr10 - 94545873 94545873 94545873 GGGAACCGGGTCCCCTCCTCTCAGAGCCTGCAATGCCGCGAGCTAACTCCTCACAACCGCTGCCG GGGAACCGGGTCCCCTCCTCTCAGAGCCTGCAGTGCCGCGAGCTAACTCCTCACAACCGCTGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:94545801..94546119 26863196 MeRIP-seq:(Medium) rs773514650 Functional Loss SNV dbSNP153 33..33 33 - - - 79623 RMVar_ID_79623 Human_SNP_ID_442842233 m1A Human chr10 - 94546417 94546417 94546417 TCTTCCTCTTCTAGCATGGCCGGGGTAATCACAGCAGTGTCCAGTTGTTCAACCATTGCTGGAGC TCTTCCTCTTCTAGCATGGCCGGGGTAATCACGGCAGTGTCCAGTTGTTCAACCATTGCTGGAGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:94546376..94546500 32194978 MeRIP-seq:(Medium) rs772100877 Functional Loss SNV dbSNP153 33..33 33 - - - 79624 RMVar_ID_79624 Human_SNP_ID_442842244 m1A Human chr10 + 94546438 94546438 94546438 CTGGACACTGCTGTGATTACCCCGGCCATGCTAGAAGAGGAAGAACAGCTTGAAGCTGCTGGACT CTGGACACTGCTGTGATTACCCCGGCCATGCTGGAAGAGGAAGAACAGCTTGAAGCTGCTGGACT A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:94546339..94546475 26863196 MeRIP-seq:(Medium) rs1452161793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385611,Human_RBP_ID_862608,Human_RBP_ID_1452068,Human_RBP_ID_4144662,Human_RBP_ID_6018551,Human_RBP_ID_8342197,Human_RBP_ID_9360585,Human_RBP_ID_11469354,Human_RBP_ID_18970966,Human_RBP_ID_22886898,Human_RBP_ID_26315959,Human_RBP_ID_27802256 Human_Splice_Rec_1161836,Human_Splice_Rec_1161837,Human_Splice_Rec_1161878,Human_Splice_Rec_1161879,Human_Splice_Rec_1161892,Human_Splice_Rec_1161893,Human_Splice_Rec_1161898,Human_Splice_Rec_1161899,Human_Splice_Rec_1161942,Human_Splice_Rec_1161943 RMVar_hsa_circ_51221,RMVar_hsa_circ_77960,RMVar_hsa_circ_145215,RMVar_hsa_circ_362221 79625 RMVar_ID_79625 Human_SNP_ID_442844535 m1A Human chr10 + 94555394 94555394 94555394 AGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCACCCCTGGACTCCAGCCTGGATGACAGAGTGAG AGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCCCCCCTGGACTCCAGCCTGGATGACAGAGTGAG A C HELLS Ensembl:ENSG00000119969 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:94555308..94555459 26863196 MeRIP-seq:(Medium) rs976952733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616259,Human_RBP_ID_22885947,Human_RBP_ID_24862362 RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551,RMVar_hsa_circ_319734 79626 RMVar_ID_79626 Human_SNP_ID_443035051 m1A Human chr10 - 95237869 95237869 95237869 TCCAGCAGGCCTCTGCTGCAGCTTTTTCTCTCAGTGTTCTGGCCCTCTCCTCTCTTGAAAGTTCT TCCAGCAGGCCTCTGCTGCAGCTTTTTCTCTCGGTGTTCTGGCCCTCTCCTCTCTTGAAAGTTCT T C PDLIM1 Ensembl:ENSG00000107438 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:95237820..95238575 32194978 MeRIP-seq:(Medium) rs957632431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385840,Human_RBP_ID_5110032,Human_RBP_ID_5138349,Human_RBP_ID_8342499,Human_RBP_ID_17228746,Human_RBP_ID_17461810,Human_RBP_ID_17648171,Human_RBP_ID_18601143,Human_RBP_ID_18931750,Human_RBP_ID_23478627,Human_RBP_ID_24402575 Human_miRNA_ID_285933,Human_miRNA_ID_523965,Human_miRNA_ID_2059967,Human_miRNA_ID_2185363,Human_miRNA_ID_2370054,Human_miRNA_ID_2662209,Human_miRNA_ID_2680662,Human_miRNA_ID_2706337 RMVar_hsa_circ_106573,RMVar_hsa_circ_112475,RMVar_hsa_circ_115700,RMVar_hsa_circ_109446,RMVar_hsa_circ_145232,RMVar_hsa_circ_95545,RMVar_hsa_circ_99590,RMVar_hsa_circ_145234,RMVar_hsa_circ_145235,RMVar_hsa_circ_145236,RMVar_hsa_circ_145233,RMVar_hsa_circ_145231 79627 RMVar_ID_79627 Human_SNP_ID_443037199 m1A Human chr10 - 95247220 95247220 95247220 CTTGGTTTTGCAGGAAATCCTGGAGTCTGAAGAAAAAGGTAATCAGCTCCATCTGCAGTCAGAGG CTTGGTTTTGCAGGAAATCCTGGAGTCTGAAGGAAAAGGTAATCAGCTCCATCTGCAGTCAGAGG T C PDLIM1 Ensembl:ENSG00000107438 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044607406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385850,Human_RBP_ID_861646,Human_RBP_ID_5340691,Human_RBP_ID_8995514 Human_Splice_Rec_1162419,Human_Splice_Rec_1162431,Human_Splice_Rec_1162435 RMVar_hsa_circ_106573,RMVar_hsa_circ_112475,RMVar_hsa_circ_115700,RMVar_hsa_circ_109446,RMVar_hsa_circ_145232,RMVar_hsa_circ_145234,RMVar_hsa_circ_145233,RMVar_hsa_circ_54795,RMVar_hsa_circ_376904,RMVar_hsa_circ_145231,RMVar_hsa_circ_300888,RMVar_hsa_circ_145237,RMVar_hsa_circ_125677 79628 RMVar_ID_79628 Human_SNP_ID_443037565 m1A Human chr10 - 95248822 95248822 95248822 AGGGCATTGCAGGCTGAGGGTGCAGTAAGTGCATAGGCTGTGAAGCTAGTGTTTCCCAGGCACAG AGGGCATTGCAGGCTGAGGGTGCAGTAAGTGCGTAGGCTGTGAAGCTAGTGTTTCCCAGGCACAG T C PDLIM1 Ensembl:ENSG00000107438 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:95248820..95248977 26863196 MeRIP-seq:(Medium) rs759061893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_109446,RMVar_hsa_circ_145232,RMVar_hsa_circ_145233,RMVar_hsa_circ_54795,RMVar_hsa_circ_376904,RMVar_hsa_circ_145231,RMVar_hsa_circ_145237,RMVar_hsa_circ_125677 79629 RMVar_ID_79629 Human_SNP_ID_443041095 m1A Human chr10 - 95263960 95263960 95263960 TACTGCCAGGGTCATCACAAACCAGTACAACAACCCAGCTGGCCTCTACTCTTCTGAAAATATCT TACTGCCAGGGTCATCACAAACCAGTACAACAGCCCAGCTGGCCTCTACTCTTCTGAAAATATCT T C PDLIM1 Ensembl:ENSG00000107438 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:95263909..95264021 26863196 MeRIP-seq:(Medium) rs749725911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17230188,Human_RBP_ID_18187977,Human_RBP_ID_26802177 Human_Splice_Rec_1162417,Human_Splice_Rec_1162429 RMVar_hsa_circ_56183,RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_109446,RMVar_hsa_circ_145232,RMVar_hsa_circ_145233,RMVar_hsa_circ_54795,RMVar_hsa_circ_376904,RMVar_hsa_circ_145231,RMVar_hsa_circ_145237,RMVar_hsa_circ_125677,RMVar_hsa_circ_325104,RMVar_hsa_circ_145238 79630 RMVar_ID_79630 Human_SNP_ID_443041106 m1A Human chr10 - 95263991 95263991 95263991 TGCCCTTTACCGCCTCGCCTGCCTCCAGCACTACTGCCAGGGTCATCACAAACCAGTACAACAAC TGCCCTTTACCGCCTCGCCTGCCTCCAGCACTGCTGCCAGGGTCATCACAAACCAGTACAACAAC T C PDLIM1 Ensembl:ENSG00000107438 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:95263940..95264105 26863196 MeRIP-seq:(Medium) rs200895548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385857,Human_RBP_ID_17230188,Human_RBP_ID_18187977,Human_RBP_ID_26802834 Human_Splice_Rec_1162416,Human_Splice_Rec_1162428,Human_Splice_Rec_1162442 Human_miRNA_ID_2173542,Human_miRNA_ID_2176986,Human_miRNA_ID_2355482,Human_miRNA_ID_2774698 RMVar_hsa_circ_56183,RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_109446,RMVar_hsa_circ_145232,RMVar_hsa_circ_145233,RMVar_hsa_circ_54795,RMVar_hsa_circ_376904,RMVar_hsa_circ_145231,RMVar_hsa_circ_145237,RMVar_hsa_circ_125677,RMVar_hsa_circ_325104,RMVar_hsa_circ_145238 79631 RMVar_ID_79631 Human_SNP_ID_443047433 m1A Human chr10 - 95290915 95290915 95290915 CCCCGCGGGTCGTCGCCCGCCACAGCCGCGCCATGACCACCCAGCAGATAGACCTCCAGGGCCCG CCCCGCGGGTCGTCGCCCGCCACAGCCGCGCCGTGACCACCCAGCAGATAGACCTCCAGGGCCCG T C PDLIM1 Ensembl:ENSG00000107438 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:95290865..95291050 26863196 MeRIP-seq:(Medium) rs1422832382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136432,Human_RBP_ID_9320983,Human_RBP_ID_22157194 Human_Splice_Rec_1162411,Human_Splice_Rec_1162425 Human_miRNA_ID_2975650 RMVar_hsa_circ_115700,RMVar_hsa_circ_145231 79632 RMVar_ID_79632 Human_SNP_ID_443047434 m1A Human chr10 - 95290915 95290915 95290915 CCCCGCGGGTCGTCGCCCGCCACAGCCGCGCCATGACCACCCAGCAGATAGACCTCCAGGGCCCG CCCCGCGGGTCGTCGCCCGCCACAGCCGCGCCCTGACCACCCAGCAGATAGACCTCCAGGGCCCG T G PDLIM1 Ensembl:ENSG00000107438 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:95290865..95291050 26863196 MeRIP-seq:(Medium) rs1422832382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136432,Human_RBP_ID_9320983,Human_RBP_ID_22157194 Human_Splice_Rec_1162411,Human_Splice_Rec_1162425 Human_miRNA_ID_2975650 RMVar_hsa_circ_115700,RMVar_hsa_circ_145231 79633 RMVar_ID_79633 Human_SNP_ID_443122938 m1A Human chr10 - 95614082 95614082 95614082 GATAGATCTGATCATTCCACGTGGCTCTTCCCAGCTGGTCAGAGACATCCAGAAAGCTGCTAAGG GATAGATCTGATCATTCCACGTGGCTCTTCCCGGCTGGTCAGAGACATCCAGAAAGCTGCTAAGG T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:95613951..95614082 32194978 MeRIP-seq:(Medium) rs1242728015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1773817,Human_RBP_ID_8764407 Human_Splice_Rec_1163246,Human_Splice_Rec_1163280,Human_Splice_Rec_1163290 RMVar_hsa_circ_12348,RMVar_hsa_circ_107199,RMVar_hsa_circ_269363,RMVar_hsa_circ_292008,RMVar_hsa_circ_145266,RMVar_hsa_circ_17352,RMVar_hsa_circ_145267 79634 RMVar_ID_79634 Human_SNP_ID_443132270 m1A Human chr10 + 95653401 95653401 95653401 ACTCAACATGCTGCGATGTGGTCACTAACCAAAGTATCTGCAGAATACATTTTTTAAAAAGTGAG ACTCAACATGCTGCGATGTGGTCACTAACCAACGTATCTGCAGAATACATTTTTTAAAAAGTGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:95653351..95653471 26863196 MeRIP-seq:(Medium) rs1369588770 Functional Loss SNV dbSNP153 33..33 33 - - - 79635 RMVar_ID_79635 Human_SNP_ID_443133107 m1A Human chr10 + 95656632 95656632 95656632 CCTCACCACCGCCGCCTTCGCCCCCTGGCACTACCGCGGGTCCGCACTCCACGCCGGGCTGATTC CCTCACCACCGCCGCCTTCGCCCCCTGGCACTTCCGCGGGTCCGCACTCCACGCCGGGCTGATTC A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:95656607..95656691 26863410 MeRIP-seq:(Medium) rs1485814793 Functional Loss SNV dbSNP153 33..33 33 - - - 79636 RMVar_ID_79636 Human_SNP_ID_443133116 m1A Human chr10 - 95656647 95656647 95656647 AGTGAGCGAGCGCCGGAATCAGCCCGGCGTGGAGTGCGGACCCGCGGTAGTGCCAGGGGGCGAAG AGTGAGCGAGCGCCGGAATCAGCCCGGCGTGGGGTGCGGACCCGCGGTAGTGCCAGGGGGCGAAG T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:95656552..95656773;chr10:95656496..95656832;chr10:95656526..95656802 26863196 MeRIP-seq:(Medium) rs117502632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225650,Human_RBP_ID_4133615,Human_RBP_ID_8940417,Human_RBP_ID_9273954,Human_RBP_ID_9320664,Human_RBP_ID_22431551,Human_RBP_ID_26802836 Human_Splice_Rec_1163221,Human_Splice_Rec_1163255 Clinvar_Rec_366,Clinvar_Rec_367 GWAS_ID_9543,GWAS_ID_9544,GWAS_ID_9545,GWAS_ID_9546,GWAS_ID_9547,GWAS_ID_9548,GWAS_ID_9549,GWAS_ID_9550 79637 RMVar_ID_79637 Human_SNP_ID_443133131 m1A Human chr10 - 95656679 95656677 95656679 ATCGTGCGGGACGTGGACGGAAGAAAAAAGAGAGTGAGCGAGCGCCGGAATCAGCCCGGCGTGGA ATCGTGCGGGACGTGGACGGAAGAAAAAAGAG__TGAGCGAGCGCCGGAATCAGCCCGGCGTGGA ACT A ALDH18A1 Ensembl:ENSG00000059573 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:95656576..95656774 26863196 MeRIP-seq:(Medium) rs1017734848 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4133615,Human_RBP_ID_23478813 Human_Splice_Rec_1163221,Human_Splice_Rec_1163255 79638 RMVar_ID_79638 Human_SNP_ID_443133133 m1A Human chr10 - 95656679 95656679 95656679 ATCGTGCGGGACGTGGACGGAAGAAAAAAGAGAGTGAGCGAGCGCCGGAATCAGCCCGGCGTGGA ATCGTGCGGGACGTGGACGGAAGAAAAAAGAGTGTGAGCGAGCGCCGGAATCAGCCCGGCGTGGA T A ALDH18A1 Ensembl:ENSG00000059573 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:95656576..95656774 26863196 MeRIP-seq:(Medium) rs530549648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4133615,Human_RBP_ID_23478813 Human_Splice_Rec_1163221,Human_Splice_Rec_1163255 79639 RMVar_ID_79639 Human_SNP_ID_443141950 m1A Human chr10 - 95693816 95693816 95693816 GATGGCGTCCGGCCTCAGCCCTCTTCCTCCCCATCAGGGGCAGTGCCCACGTCTTTGGAGCTGCA GATGGCGTCCGGCCTCAGCCCTCTTCCTCCCCTTCAGGGGCAGTGCCCACGTCTTTGGAGCTGCA T A TCTN3 Ensembl:ENSG00000119977 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:95693766..95693894 26863196 MeRIP-seq:(Medium) rs1166891623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135968,Human_RBP_ID_22431818 RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_121708,RMVar_hsa_circ_145280 79640 RMVar_ID_79640 Human_SNP_ID_443141962 m1A Human chr10 - 95693847 95693847 95693847 GCTCCTGCAAGTGTTCTTTCTGGTGTTCCCCGATGGCGTCCGGCCTCAGCCCTCTTCCTCCCCAT GCTCCTGCAAGTGTTCTTTCTGGTGTTCCCCGGTGGCGTCCGGCCTCAGCCCTCTTCCTCCCCAT T C TCTN3 Ensembl:ENSG00000119977 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:95693745..95693895 26863410 MeRIP-seq:(Medium) rs1182996775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4133681,Human_RBP_ID_23478857 RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_121708,RMVar_hsa_circ_145280 79641 RMVar_ID_79641 Human_SNP_ID_443141973 m1A Human chr10 - 95693870 95693870 95693870 CCCATGCGCACCCCACAGCTCGCGCTCCTGCAAGTGTTCTTTCTGGTGTTCCCCGATGGCGTCCG CCCATGCGCACCCCACAGCTCGCGCTCCTGCAGGTGTTCTTTCTGGTGTTCCCCGATGGCGTCCG T C TCTN3 Ensembl:ENSG00000119977 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:95693762..95693912 26863196 MeRIP-seq:(Medium) rs1325148037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4133683,Human_RBP_ID_23478857 RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_121708,RMVar_hsa_circ_145280 79642 RMVar_ID_79642 Human_SNP_ID_443217444 m1A Human chr10 - 96043658 96043658 96043658 CCGCCGTCGTGCGGCGGACGCCGGCCCCGCTCATGCTGCGGACAGTGGGCCGCTAAGCGCCGGCC CCGCCGTCGTGCGGCGGACGCCGGCCCCGCTCGTGCTGCGGACAGTGGGCCGCTAAGCGCCGGCC T C ENTPD1-AS1 Ensembl:ENSG00000226688 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:96043615..96043769 26863196 MeRIP-seq:(Medium) rs1318131338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97968,RMVar_hsa_circ_145286 79643 RMVar_ID_79643 Human_SNP_ID_443228264 m1A Human chr10 - 96090163 96090163 96090163 TCATGGCTGCTGTCAGTGAGGGCCCGTAATGGAGATCGAGTCAAGGGTTGCCCAGGGACACTTAA TCATGGCTGCTGTCAGTGAGGGCCCGTAATGGCGATCGAGTCAAGGGTTGCCCAGGGACACTTAA T G ENTPD1-AS1 Ensembl:ENSG00000226688 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:96090080..96090186 26863196 MeRIP-seq:(Medium) rs993085873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8342651,Human_RBP_ID_18416155 RMVar_hsa_circ_97968,RMVar_hsa_circ_145286,RMVar_hsa_circ_145299,RMVar_hsa_circ_111200 79644 RMVar_ID_79644 Human_SNP_ID_443339100 m1A Human chr10 + 96556953 96556953 96556953 TTCAGAGCTAATCTCTCTATCCTCCATGATACACTTTCTTCTCTTGGCATTCAGAACACCATACT TTCAGAGCTAATCTCTCTATCCTCCATGATACGCTTTCTTCTCTTGGCATTCAGAACACCATACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:96556908..96557098 26863196 MeRIP-seq:(Medium) rs1285231277 Functional Loss SNV dbSNP153 33..33 33 - - - 79645 RMVar_ID_79645 Human_SNP_ID_443339120 m1A Human chr10 + 96557032 96557032 96557032 AAAGCCCTTAACTGAACTCCCCTGTTCTTCCTAAACTCTTACTACTGCACCCAGGGCTTAGTCCT AAAGCCCTTAACTGAACTCCCCTGTTCTTCCTCAACTCTTACTACTGCACCCAGGGCTTAGTCCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:96556984..96557076 26863196 MeRIP-seq:(Medium) rs758787784 Functional Loss SNV dbSNP153 33..33 33 - - - 79646 RMVar_ID_79646 Human_SNP_ID_443346255 m1A Human chr10 + 96586771 96586765 96586771 GTTCGTGCTCGTCCGCCCGGGTCCGGGGCAGCAGCAGCAGCAGCAGCCACAGCGCGGCGGCCGCC GTTCGTGCTCGTCCGCCCGGGTCCGGG______GCAGCAGCAGCAGCCACAGCGCGGCGGCCGCC GGCAGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:96586726..96587025 26863196 MeRIP-seq:(Medium) rs751439116 Functional Loss DEL dbSNP153 28..33 33 - - - 79647 RMVar_ID_79647 Human_SNP_ID_443346256 m1A Human chr10 + 96586771 96586765 96586771 GTTCGTGCTCGTCCGCCCGGGTCCGGGGCAGCAGCAGCAGCAGCAGCCACAGCGCGGCGGCCGCC GTTCGTGCTCGTCCGCCCGGGTCCGGGGCA___GCAGCAGCAGCAGCCACAGCGCGGCGGCCGCC GGCAGCA GGCA - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:96586726..96587025 26863196 MeRIP-seq:(Medium) rs751439116 Functional Loss DEL dbSNP153 31..33 33 - - - 79648 RMVar_ID_79648 Human_SNP_ID_443346265 m1A Human chr10 + 96586777 96586777 96586777 GCTCGTCCGCCCGGGTCCGGGGCAGCAGCAGCAGCAGCAGCCACAGCGCGGCGGCCGCCGCCACG GCTCGTCCGCCCGGGTCCGGGGCAGCAGCAGCGGCAGCAGCCACAGCGCGGCGGCCGCCGCCACG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:96586741..96586987 26863410 MeRIP-seq:(Medium) rs1021366179 Functional Loss SNV dbSNP153 33..33 33 - - - 79649 RMVar_ID_79649 Human_SNP_ID_443346347 m1A Human chr10 - 96586892 96586892 96586892 ATCGGCCGCGGCGGAGGCGGCGGCGGCGGAGGAGGCGGCGGCGGGAGGAGGAGTCGGTGAGCCGG ATCGGCCGCGGCGGAGGCGGCGGCGGCGGAGGCGGCGGCGGCGGGAGGAGGAGTCGGTGAGCCGG T G TM9SF3 Ensembl:ENSG00000077147 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:96586826..96587025 26863196 MeRIP-seq:(Medium) rs1062176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861965,Human_RBP_ID_4135972,Human_RBP_ID_5313309,Human_RBP_ID_8940387,Human_RBP_ID_9320666,Human_RBP_ID_19576666,Human_RBP_ID_22886661 GWAS_ID_9551,GWAS_ID_9552,GWAS_ID_9553,GWAS_ID_9554,GWAS_ID_9555,GWAS_ID_9556,GWAS_ID_9557,GWAS_ID_9558,GWAS_ID_9559,GWAS_ID_9560,GWAS_ID_9561,GWAS_ID_9562,GWAS_ID_9563,GWAS_ID_9564,GWAS_ID_9565,GWAS_ID_9566,GWAS_ID_9567,GWAS_ID_9568,GWAS_ID_9569,GWAS_ID_9570,GWAS_ID_9571,GWAS_ID_9572,GWAS_ID_9573,GWAS_ID_9574,GWAS_ID_9575,GWAS_ID_9576,GWAS_ID_9577,GWAS_ID_9578,GWAS_ID_9579,GWAS_ID_9580,GWAS_ID_9581,GWAS_ID_9582,GWAS_ID_9583,GWAS_ID_9584,GWAS_ID_9585,GWAS_ID_9586,GWAS_ID_9587,GWAS_ID_9588,GWAS_ID_9589,GWAS_ID_9590,GWAS_ID_9591,GWAS_ID_9592,GWAS_ID_9593 RMVar_hsa_circ_111369,RMVar_hsa_circ_145319,RMVar_hsa_circ_116066,RMVar_hsa_circ_145326 79650 RMVar_ID_79650 Human_SNP_ID_443346367 m1A Human chr10 - 96586924 96586909 96586924 CCCGTGCGTCTGTCCGCGCCCCGTGGATGCGAATCGGCCGCGGCGGAGGCGGCGGCGGCGGAGGA CCCGTGCGTCTGTCCGCGCCCCGTGGATGCGA_______________GGCGGCGGCGGCGGAGGA CTCCGCCGCGGCCGAT C TM9SF3 Ensembl:ENSG00000077147 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:96586726..96587025 26863196 MeRIP-seq:(Medium) rs1564944147 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_805045,Human_RBP_ID_4135972,Human_RBP_ID_5313079,Human_RBP_ID_8940388,Human_RBP_ID_9320666 RMVar_hsa_circ_111369,RMVar_hsa_circ_145319,RMVar_hsa_circ_116066,RMVar_hsa_circ_145326 79651 RMVar_ID_79651 Human_SNP_ID_443346374 m1A Human chr10 - 96586924 96586924 96586924 CCCGTGCGTCTGTCCGCGCCCCGTGGATGCGAATCGGCCGCGGCGGAGGCGGCGGCGGCGGAGGA CCCGTGCGTCTGTCCGCGCCCCGTGGATGCGAGTCGGCCGCGGCGGAGGCGGCGGCGGCGGAGGA T C TM9SF3 Ensembl:ENSG00000077147 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:96586726..96587025 26863196 MeRIP-seq:(Medium) rs1242624656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805045,Human_RBP_ID_4135972,Human_RBP_ID_5313079,Human_RBP_ID_8940388,Human_RBP_ID_9320666 RMVar_hsa_circ_111369,RMVar_hsa_circ_145319,RMVar_hsa_circ_116066,RMVar_hsa_circ_145326 79652 RMVar_ID_79652 Human_SNP_ID_443384202 m1A Human chr10 + 96750323 96750323 96750323 GCGGAGGTGCAGGTCCTGGTGCTTGATGGTCGAGGCCATCTCCTGGGCCGCCTGGCGGCCATCGT GCGGAGGTGCAGGTCCTGGTGCTTGATGGTCGCGGCCATCTCCTGGGCCGCCTGGCGGCCATCGT A C RPL13AP5 Ensembl:ENSG00000236552 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs895733370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_386383,Human_RBP_ID_4137392,Human_RBP_ID_8244924 Human_miRNA_ID_1902565 79653 RMVar_ID_79653 Human_SNP_ID_443384251 m1A Human chr10 - 96750441 96750441 96750441 CATCCGCTTGCGGAGGAAAGCCAGGTACTTCAACTTGTTTCTGTAGAAATTGCCAGAAATGTTGA CATCCGCTTGCGGAGGAAAGCCAGGTACTTCACCTTGTTTCTGTAGAAATTGCCAGAAATGTTGA T G lnc-PIK3AP1-2 RNACentral:URS00008BED02 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:96750334..96750500 26863196 MeRIP-seq:(Medium) rs1191448245 Functional Loss SNV dbSNP153 33..33 33 - - - 79654 RMVar_ID_79654 Human_SNP_ID_443384261 m1A Human chr10 + 96750474 96750474 96750474 TGAAGTACCTGGCTTTCCTCCGCAAGCGGATGAACACCAACCCTTCCCGAGTCCCCTACCACTTC TGAAGTACCTGGCTTTCCTCCGCAAGCGGATGGACACCAACCCTTCCCGAGTCCCCTACCACTTC A G RPL13AP5 Ensembl:ENSG00000236552 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1220047659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_386387,Human_RBP_ID_3938507,Human_RBP_ID_4137393,Human_RBP_ID_5164710,Human_RBP_ID_17230346,Human_RBP_ID_17559559,Human_RBP_ID_18187979,Human_RBP_ID_26802845 Human_miRNA_ID_1848432 79655 RMVar_ID_79655 Human_SNP_ID_443406086 m1A Human chr10 + 96832318 96832318 96832318 CGGGCGGGCGGCAGAAGATGGCGAGGGTGTGTAGGCGGCAGCAATGCTCCGTTGAGAGACGCGGC CGGGCGGGCGGCAGAAGATGGCGAGGGTGTGTCGGCGGCAGCAATGCTCCGTTGAGAGACGCGGC A C LCOR Ensembl:ENSG00000196233 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:96831944..96832393;chr10:96831979..96832456;chr10:96831995..96832380 26863196 MeRIP-seq:(Medium) rs1428930114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_386391,Human_RBP_ID_4134237,Human_RBP_ID_6022399,Human_RBP_ID_11478297,Human_RBP_ID_18416157,Human_RBP_ID_18970994 Human_Splice_Rec_1164601,Human_Splice_Rec_1164615,Human_Splice_Rec_1164629 RMVar_hsa_circ_113816,RMVar_hsa_circ_145347 79656 RMVar_ID_79656 Human_SNP_ID_443406465 m1A Human chr10 - 96833040 96833040 96833040 AGGAAGTGCAGCCGCTGCCCCCCGCGGCCATGACACCCCACTTGGCTCGGTCAGGCGCACCCGGG AGGAAGTGCAGCCGCTGCCCCCCGCGGCCATGGCACCCCACTTGGCTCGGTCAGGCGCACCCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:96833031..96833162 26863196 MeRIP-seq:(Medium) rs1217948380 Functional Loss SNV dbSNP153 33..33 33 - - - 79657 RMVar_ID_79657 Human_SNP_ID_443528707 m1A Human chr10 + 97319521 97319521 97319521 CGAGGAGGCGGAGGGGGAGGAAGAGGAGGAGGACAGCTTCCTCCTACTGCAGCAGTCAGTGGCGC CGAGGAGGCGGAGGGGGAGGAAGAGGAGGAGGGCAGCTTCCTCCTACTGCAGCAGTCAGTGGCGC A G FRAT1 Ensembl:ENSG00000165879 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:97319308..97319634;chr10:97319316..97319646 26863196 MeRIP-seq:(Medium) rs1328128605 Functional Loss SNV dbSNP153 33..33 33 - - - 79658 RMVar_ID_79658 Human_SNP_ID_443529264 m1A Human chr10 + 97321038 97321038 97321038 TGAACCCCACGCCCTGTCTAAAGTGTATTTTCAGAGCCGGCCCGCCTCTCCTCGGTTCAAGGTCA TGAACCCCACGCCCTGTCTAAAGTGTATTTTCGGAGCCGGCCCGCCTCTCCTCGGTTCAAGGTCA A G FRAT1 Ensembl:ENSG00000165879 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:97320989..97321116 26863196 MeRIP-seq:(Medium) rs1363601522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17786414 79659 RMVar_ID_79659 Human_SNP_ID_443532509 m1A Human chr10 - 97333325 97333325 97333325 GGGTGGCTTGGCATTGCCCCTTTTTCCCACCGATTCGGTGGCTGGTGAAGGTGGGAGATGTGAAC GGGTGGCTTGGCATTGCCCCTTTTTCCCACCGCTTCGGTGGCTGGTGAAGGTGGGAGATGTGAAC T G FRAT2 Ensembl:ENSG00000181274 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97333276..97333375 26863196 MeRIP-seq:(Medium) rs1203915859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_386743,Human_RBP_ID_5138029,Human_RBP_ID_8173428,Human_RBP_ID_26398570 79660 RMVar_ID_79660 Human_SNP_ID_443532599 m1A Human chr10 + 97333669 97333669 97333669 TTCTCATGCCCCACGGAAGCACCCTGGCGCATACATTTCTCCACGCTTAAGTTTTCTCCGACGGC TTCTCATGCCCCACGGAAGCACCCTGGCGCATGCATTTCTCCACGCTTAAGTTTTCTCCGACGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:97333621..97334075 26863196 MeRIP-seq:(Medium) rs1322264004 Functional Loss SNV dbSNP153 33..33 33 - - - 79661 RMVar_ID_79661 Human_SNP_ID_443532732 m1A Human chr10 + 97333965 97333965 97333965 GCCCAGGGGCGCTTGCGGGGCCCGTGGCTGCAACCGCGGCGACGGCTCGTTGGAGTCTCCGCACG GCCCAGGGGCGCTTGCGGGGCCCGTGGCTGCAGCCGCGGCGACGGCTCGTTGGAGTCTCCGCACG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:97333551..97334025 26863196 MeRIP-seq:(Medium) rs1404610557 Functional Loss SNV dbSNP153 33..33 33 - - - 79662 RMVar_ID_79662 Human_SNP_ID_443533065 m1A Human chr10 - 97334585 97334585 97334585 CCCCCAGCGAAGCCCGCACAGCTCCGGGTGCCAGGACGGGGGGCCATGCCGTGCCGGAGGGAGGA CCCCCAGCGAAGCCCGCACAGCTCCGGGTGCCTGGACGGGGGGCCATGCCGTGCCGGAGGGAGGA T A FRAT2 Ensembl:ENSG00000181274 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:97334398..97334700 26863196 MeRIP-seq:(Medium) rs1265130623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136970 79663 RMVar_ID_79663 Human_SNP_ID_443533066 m1A Human chr10 - 97334585 97334585 97334585 CCCCCAGCGAAGCCCGCACAGCTCCGGGTGCCAGGACGGGGGGCCATGCCGTGCCGGAGGGAGGA CCCCCAGCGAAGCCCGCACAGCTCCGGGTGCCGGGACGGGGGGCCATGCCGTGCCGGAGGGAGGA T C FRAT2 Ensembl:ENSG00000181274 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:97334398..97334700 26863196 MeRIP-seq:(Medium) rs1265130623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136970 79664 RMVar_ID_79664 Human_SNP_ID_443539928 m1A Human chr10 - 97360578 97360578 97360578 CCAGAAGCTCAAGCACCAGAAAGAGGCTGAGGAGGAGGAGCTGGAGATACCCCCTCAGTACCAAG CCAGAAGCTCAAGCACCAGAAAGAGGCTGAGGGGGAGGAGCTGGAGATACCCCCTCAGTACCAAG T C RRP12 Ensembl:ENSG00000052749 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:97358994..97363864 32194978 MeRIP-seq:(Medium) rs1305993694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3938510,Human_RBP_ID_9360611,Human_RBP_ID_26316553 Human_Splice_Rec_1165078,Human_Splice_Rec_1165079,Human_Splice_Rec_1165110,Human_Splice_Rec_1165111,Human_Splice_Rec_1165176,Human_Splice_Rec_1165177,Human_Splice_Rec_1165244,Human_Splice_Rec_1165245,Human_Splice_Rec_1165304,Human_Splice_Rec_1165305,Human_Splice_Rec_1165366,Human_Splice_Rec_1165367,Human_Splice_Rec_1165374,Human_Splice_Rec_1165375 RMVar_hsa_circ_80835,RMVar_hsa_circ_99370,RMVar_hsa_circ_108764,RMVar_hsa_circ_105137,RMVar_hsa_circ_93114,RMVar_hsa_circ_89390,RMVar_hsa_circ_145386,RMVar_hsa_circ_145388,RMVar_hsa_circ_145390,RMVar_hsa_circ_145389,RMVar_hsa_circ_145387,RMVar_hsa_circ_145385 79665 RMVar_ID_79665 Human_SNP_ID_443540768 m1A Human chr10 + 97363896 97363896 97363896 ATCACATCTTCCATTGGGTCAGCCATCTCTTCATCTTCGCCTGGAGCCAAAAAAGAGAGGCCCAT ATCACATCTTCCATTGGGTCAGCCATCTCTTCGTCTTCGCCTGGAGCCAAAAAAGAGAGGCCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97360579..97365950 26863196 MeRIP-seq:(Medium) rs374639098 Functional Loss SNV dbSNP153 33..33 33 - - - 79666 RMVar_ID_79666 Human_SNP_ID_443541543 m1A Human chr10 - 97366580 97366580 97366580 GATTTTAGCTGACTCAGAGGACGAGGAGGACAATGAGGAGGAGGAAAGAAGCCGAGGCAAGGAGC GATTTTAGCTGACTCAGAGGACGAGGAGGACAGTGAGGAGGAGGAAAGAAGCCGAGGCAAGGAGC T C RRP12 Ensembl:ENSG00000052749 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:97366445..97366687 26863196 MeRIP-seq:(Medium) rs776832580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26084,Human_RBP_ID_4134954,Human_RBP_ID_22157450,Human_RBP_ID_26316556 Human_Splice_Rec_1165072,Human_Splice_Rec_1165104,Human_Splice_Rec_1165170,Human_Splice_Rec_1165238,Human_Splice_Rec_1165298,Human_Splice_Rec_1165360 RMVar_hsa_circ_80835,RMVar_hsa_circ_99370,RMVar_hsa_circ_108764,RMVar_hsa_circ_105137,RMVar_hsa_circ_93114,RMVar_hsa_circ_89390,RMVar_hsa_circ_100974,RMVar_hsa_circ_145386,RMVar_hsa_circ_145388,RMVar_hsa_circ_145390,RMVar_hsa_circ_145389,RMVar_hsa_circ_145387,RMVar_hsa_circ_145385,RMVar_hsa_circ_122412,RMVar_hsa_circ_145393,RMVar_hsa_circ_145394 79667 RMVar_ID_79667 Human_SNP_ID_443541676 m1A Human chr10 - 97366830 97366830 97366830 TGGTCAACATCCGGAAAGCTGAGGCCCGGGCCAAGAGGCACCGAGCCCTGAGCCAGGCTGCCGTG TGGTCAACATCCGGAAAGCTGAGGCCCGGGCCGAGAGGCACCGAGCCCTGAGCCAGGCTGCCGTG T C RRP12 Ensembl:ENSG00000052749 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:97366780..97366881 32194978 MeRIP-seq:(Medium) rs1442772137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22886901 Human_Splice_Rec_1165070,Human_Splice_Rec_1165071,Human_Splice_Rec_1165102,Human_Splice_Rec_1165103,Human_Splice_Rec_1165168,Human_Splice_Rec_1165169,Human_Splice_Rec_1165236,Human_Splice_Rec_1165237,Human_Splice_Rec_1165296,Human_Splice_Rec_1165297,Human_Splice_Rec_1165358,Human_Splice_Rec_1165359 RMVar_hsa_circ_80835,RMVar_hsa_circ_99370,RMVar_hsa_circ_108764,RMVar_hsa_circ_105137,RMVar_hsa_circ_93114,RMVar_hsa_circ_89390,RMVar_hsa_circ_100974,RMVar_hsa_circ_145386,RMVar_hsa_circ_145388,RMVar_hsa_circ_145390,RMVar_hsa_circ_145389,RMVar_hsa_circ_145387,RMVar_hsa_circ_145385,RMVar_hsa_circ_122412,RMVar_hsa_circ_145393,RMVar_hsa_circ_145394 79668 RMVar_ID_79668 Human_SNP_ID_443551721 m1A Human chr10 + 97401253 97401253 97401253 GAGCGACCCATGTTGACTAAGCCGTGGCGAGGAATGAGCTTAAATGACCGGCTTCCAGGGACGTA GAGCGACCCATGTTGACTAAGCCGTGGCGAGGTATGAGCTTAAATGACCGGCTTCCAGGGACGTA A T AL355490.3 Ensembl:ENSG00000231970 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97401203..97401354 32194978 MeRIP-seq:(Medium) rs557141106 Functional Loss SNV dbSNP153 33..33 33 - - - 79669 RMVar_ID_79669 Human_SNP_ID_443558688 m1A Human chr10 + 97426232 97426232 97426232 CGCGGGAGCCGGACTGAGCGGTGCGAGCGCGCAGGCGCGGCCGACGGGGCGGGCTGCTACTCCGG CGCGGGAGCCGGACTGAGCGGTGCGAGCGCGCGGGCGCGGCCGACGGGGCGGGCTGCTACTCCGG A G PGAM1 Ensembl:ENSG00000171314 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:97426151..97426308;chr10:97426176..97426319 26863196 MeRIP-seq:(Medium) rs1476363245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225950,Human_RBP_ID_4135069,Human_RBP_ID_9273963,Human_RBP_ID_9320670,Human_RBP_ID_17345741,Human_RBP_ID_22431553 79670 RMVar_ID_79670 Human_SNP_ID_443558807 m1A Human chr10 + 97426423 97426423 97426423 CGACCTGAGCCCGGCGGGCCACGAGGAGGCGAAGCGCGGCGGGCAGGCGCTACGAGGTGCGGAGG CGACCTGAGCCCGGCGGGCCACGAGGAGGCGACGCGCGGCGGGCAGGCGCTACGAGGTGCGGAGG A C PGAM1 Ensembl:ENSG00000171314 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97426410..97426479 26863196 MeRIP-seq:(Medium) rs893710648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225951,Human_RBP_ID_19045630 Human_Splice_Rec_1165423,Human_Splice_Rec_1165429 79671 RMVar_ID_79671 Human_SNP_ID_443558808 m1A Human chr10 + 97426423 97426423 97426423 CGACCTGAGCCCGGCGGGCCACGAGGAGGCGAAGCGCGGCGGGCAGGCGCTACGAGGTGCGGAGG CGACCTGAGCCCGGCGGGCCACGAGGAGGCGAGGCGCGGCGGGCAGGCGCTACGAGGTGCGGAGG A G PGAM1 Ensembl:ENSG00000171314 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97426410..97426479 26863196 MeRIP-seq:(Medium) rs893710648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225951,Human_RBP_ID_19045630 Human_Splice_Rec_1165423,Human_Splice_Rec_1165429 79672 RMVar_ID_79672 Human_SNP_ID_443558817 m1A Human chr10 + 97426445 97426445 97426445 GAGGAGGCGAAGCGCGGCGGGCAGGCGCTACGAGGTGCGGAGGGGCCGGGTGTGGGCTGCGAAGG GAGGAGGCGAAGCGCGGCGGGCAGGCGCTACGTGGTGCGGAGGGGCCGGGTGTGGGCTGCGAAGG A T PGAM1 Ensembl:ENSG00000171314 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:97426176..97426502 26863410 MeRIP-seq:(Medium) rs143826593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225951,Human_RBP_ID_19045630,Human_RBP_ID_22536715 Human_Splice_Rec_1165423,Human_Splice_Rec_1165429 79673 RMVar_ID_79673 Human_SNP_ID_443561730 m1A Human chr10 - 97437196 97437194 97437196 GAACGAGCTGGGAGTGGTGGTAGCCCACAGTGAGTCAGGTGAGATGGCCTTGTTTCCACATCCTT GAACGAGCTGGGAGTGGTGGTAGCCCACAGTG__TCAGGTGAGATGGCCTTGTTTCCACATCCTT ACT A EXOSC1 Ensembl:ENSG00000171311 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97436440..97437230 32194978 MeRIP-seq:(Medium) rs1182217490 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_225468,Human_RBP_ID_26802200 Human_Splice_Rec_1165448,Human_Splice_Rec_1165449,Human_Splice_Rec_1165460,Human_Splice_Rec_1165461,Human_Splice_Rec_1165472,Human_Splice_Rec_1165473,Human_Splice_Rec_1165500,Human_Splice_Rec_1165501,Human_Splice_Rec_1165516,Human_Splice_Rec_1165517,Human_Splice_Rec_1165528 Human_miRNA_ID_2453980 RMVar_hsa_circ_145409,RMVar_hsa_circ_119326,RMVar_hsa_circ_269206,RMVar_hsa_circ_145411,RMVar_hsa_circ_377951,RMVar_hsa_circ_145408,RMVar_hsa_circ_145412,RMVar_hsa_circ_145410,RMVar_hsa_circ_145414,RMVar_hsa_circ_113427,RMVar_hsa_circ_284973,RMVar_hsa_circ_291947,RMVar_hsa_circ_303809,RMVar_hsa_circ_275276,RMVar_hsa_circ_145416,RMVar_hsa_circ_145417,RMVar_hsa_circ_145415,RMVar_hsa_circ_145413 79674 RMVar_ID_79674 Human_SNP_ID_443561731 m1A Human chr10 - 97437196 97437196 97437196 GAACGAGCTGGGAGTGGTGGTAGCCCACAGTGAGTCAGGTGAGATGGCCTTGTTTCCACATCCTT GAACGAGCTGGGAGTGGTGGTAGCCCACAGTGGGTCAGGTGAGATGGCCTTGTTTCCACATCCTT T C EXOSC1 Ensembl:ENSG00000171311 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97436440..97437230 32194978 MeRIP-seq:(Medium) rs1391159719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225468,Human_RBP_ID_26802200 Human_Splice_Rec_1165448,Human_Splice_Rec_1165449,Human_Splice_Rec_1165460,Human_Splice_Rec_1165461,Human_Splice_Rec_1165472,Human_Splice_Rec_1165473,Human_Splice_Rec_1165500,Human_Splice_Rec_1165501,Human_Splice_Rec_1165516,Human_Splice_Rec_1165517,Human_Splice_Rec_1165528 Human_miRNA_ID_2453980 RMVar_hsa_circ_145409,RMVar_hsa_circ_119326,RMVar_hsa_circ_269206,RMVar_hsa_circ_145411,RMVar_hsa_circ_377951,RMVar_hsa_circ_145408,RMVar_hsa_circ_145412,RMVar_hsa_circ_145410,RMVar_hsa_circ_145414,RMVar_hsa_circ_113427,RMVar_hsa_circ_284973,RMVar_hsa_circ_291947,RMVar_hsa_circ_303809,RMVar_hsa_circ_275276,RMVar_hsa_circ_145416,RMVar_hsa_circ_145417,RMVar_hsa_circ_145415,RMVar_hsa_circ_145413 79675 RMVar_ID_79675 Human_SNP_ID_443564003 m1A Human chr10 - 97445803 97445803 97445803 GTAACTTGGAGGAGGGCAGCCCGGGCAGCGGCACCTACACCCGCCACGGCTACATCTTTTCGTCG GTAACTTGGAGGAGGGCAGCCCGGGCAGCGGCCCCTACACCCGCCACGGCTACATCTTTTCGTCG T G EXOSC1 Ensembl:ENSG00000171311 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97445722..97445823 32194978 MeRIP-seq:(Medium) rs748917834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225469,Human_RBP_ID_806130,Human_RBP_ID_4145136,Human_RBP_ID_18970184,Human_RBP_ID_22432578 Human_Splice_Rec_1165438,Human_Splice_Rec_1165439,Human_Splice_Rec_1165452,Human_Splice_Rec_1165453,Human_Splice_Rec_1165464,Human_Splice_Rec_1165465,Human_Splice_Rec_1165476,Human_Splice_Rec_1165477,Human_Splice_Rec_1165485,Human_Splice_Rec_1165494,Human_Splice_Rec_1165495,Human_Splice_Rec_1165504,Human_Splice_Rec_1165505,Human_Splice_Rec_1165519,Human_Splice_Rec_1165530,Human_Splice_Rec_1165531,Human_Splice_Rec_1165536,Human_Splice_Rec_1165537 Human_miRNA_ID_2027283 RMVar_hsa_circ_113427,RMVar_hsa_circ_145417 79676 RMVar_ID_79676 Human_SNP_ID_443564189 m1A Human chr10 - 97446245 97446245 97446245 CTCGGCGCCCCGGCCGGGCCCGGCTCAATCCAAACCACCATGGCCCGCCGCCCGCAGCGCCAGGC CTCGGCGCCCCGGCCGGGCCCGGCTCAATCCACACCACCATGGCCCGCCGCCCGCAGCGCCAGGC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:97446189..97446288 26863410 MeRIP-seq:(Medium) rs1192645252 Functional Loss SNV dbSNP153 33..33 33 - - - 79677 RMVar_ID_79677 Human_SNP_ID_443564223 m1A Human chr10 - 97446329 97446329 97446329 GCCCTTACCTGCCGCCTGCCGACTCCCCAGTCAGCCAAACCGAGCCCCGTAGCCTCTGCCGCCGC GCCCTTACCTGCCGCCTGCCGACTCCCCAGTCGGCCAAACCGAGCCCCGTAGCCTCTGCCGCCGC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:97446229..97448215 26863410 MeRIP-seq:(Medium) rs1355439738 Functional Loss SNV dbSNP153 33..33 33 - - - 79678 RMVar_ID_79678 Human_SNP_ID_443567060 m1A Human chr10 + 97456924 97456924 97456924 GCTGGACTGTGTCAGCCACGACTCGAGCACTCATTCTGCTCCCTATGTTATTTCAAGGGCCTCCA GCTGGACTGTGTCAGCCACGACTCGAGCACTCTTTCTGCTCCCTATGTTATTTCAAGGGCCTCCA A T ZDHHC16 Ensembl:ENSG00000171307 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97456873..97457271 32194978 MeRIP-seq:(Medium) rs779157688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8343059,Human_RBP_ID_11482610,Human_RBP_ID_17462070,Human_RBP_ID_17681022,Human_RBP_ID_18246207 79679 RMVar_ID_79679 Human_SNP_ID_443567987 m1A Human chr10 + 97459740 97459740 97459740 TGAGAAAGACCCTTCAAGTAGTTTGGCTTCACATCTGTAAAAAATGGAAAGGCTTAGGGGAGAAA TGAGAAAGACCCTTCAAGTAGTTTGGCTTCACGTCTGTAAAAAATGGAAAGGCTTAGGGGAGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97459654..97459755 32194978 MeRIP-seq:(Medium) rs1282343653 Functional Loss SNV dbSNP153 33..33 33 - - - 79680 RMVar_ID_79680 Human_SNP_ID_443568360 m1A Human chr10 - 97460933 97460933 97460933 TGGAGGCTGGCCTGGGCTCTGGGCCCTGTCGTAGTCAGGCCTTCACTCTTCTTCTCTGGGTAAGG TGGAGGCTGGCCTGGGCTCTGGGCCCTGTCGTTGTCAGGCCTTCACTCTTCTTCTCTGGGTAAGG T A MMS19 Ensembl:ENSG00000155229 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97460728..97461034 32194978 MeRIP-seq:(Medium) rs1482588145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135184,Human_RBP_ID_5340736,Human_RBP_ID_18187982,Human_RBP_ID_22789360,Human_RBP_ID_24851893 Human_Splice_Rec_1165820,Human_Splice_Rec_1165821,Human_Splice_Rec_1165854,Human_Splice_Rec_1165855,Human_Splice_Rec_1165912,Human_Splice_Rec_1165913,Human_Splice_Rec_1165972,Human_Splice_Rec_1165973,Human_Splice_Rec_1166034,Human_Splice_Rec_1166035,Human_Splice_Rec_1166096,Human_Splice_Rec_1166097,Human_Splice_Rec_1166154,Human_Splice_Rec_1166155,Human_Splice_Rec_1166169 Human_miRNA_ID_109081,Human_miRNA_ID_836416 RMVar_hsa_circ_89563,RMVar_hsa_circ_106110,RMVar_hsa_circ_145421,RMVar_hsa_circ_145424,RMVar_hsa_circ_106951,RMVar_hsa_circ_145422,RMVar_hsa_circ_111611,RMVar_hsa_circ_145425,RMVar_hsa_circ_145427,RMVar_hsa_circ_92398,RMVar_hsa_circ_145429,RMVar_hsa_circ_309079,RMVar_hsa_circ_145428,RMVar_hsa_circ_114477,RMVar_hsa_circ_312888,RMVar_hsa_circ_359494,RMVar_hsa_circ_145431,RMVar_hsa_circ_287289,RMVar_hsa_circ_145430,RMVar_hsa_circ_49917 79681 RMVar_ID_79681 Human_SNP_ID_443568750 m1A Human chr10 - 97462094 97462094 97462094 CCCCCAGGTTAGCTGCCCAGAGTGTGACACACATTGTGCCCCTCTTCTTGGATGGCAACGTGTCC CCCCCAGGTTAGCTGCCCAGAGTGTGACACACGTTGTGCCCCTCTTCTTGGATGGCAACGTGTCC T C MMS19 Ensembl:ENSG00000155229 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97461862..97462696 32194978 MeRIP-seq:(Medium) rs367731247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3937977,Human_RBP_ID_4145167 Human_Splice_Rec_1165816,Human_Splice_Rec_1165817,Human_Splice_Rec_1165848,Human_Splice_Rec_1165849,Human_Splice_Rec_1165906,Human_Splice_Rec_1165907,Human_Splice_Rec_1165966,Human_Splice_Rec_1165967,Human_Splice_Rec_1166028,Human_Splice_Rec_1166029,Human_Splice_Rec_1166090,Human_Splice_Rec_1166091,Human_Splice_Rec_1166148,Human_Splice_Rec_1166149,Human_Splice_Rec_1166174,Human_Splice_Rec_1166175 RMVar_hsa_circ_89563,RMVar_hsa_circ_106110,RMVar_hsa_circ_145421,RMVar_hsa_circ_145424,RMVar_hsa_circ_106951,RMVar_hsa_circ_145422,RMVar_hsa_circ_111611,RMVar_hsa_circ_145425,RMVar_hsa_circ_145427,RMVar_hsa_circ_92398,RMVar_hsa_circ_145429,RMVar_hsa_circ_309079,RMVar_hsa_circ_145428,RMVar_hsa_circ_114477,RMVar_hsa_circ_312888,RMVar_hsa_circ_359494,RMVar_hsa_circ_145431,RMVar_hsa_circ_287289,RMVar_hsa_circ_145430,RMVar_hsa_circ_145432,RMVar_hsa_circ_49917 79682 RMVar_ID_79682 Human_SNP_ID_443568751 m1A Human chr10 - 97462094 97462094 97462094 CCCCCAGGTTAGCTGCCCAGAGTGTGACACACATTGTGCCCCTCTTCTTGGATGGCAACGTGTCC CCCCCAGGTTAGCTGCCCAGAGTGTGACACACCTTGTGCCCCTCTTCTTGGATGGCAACGTGTCC T G MMS19 Ensembl:ENSG00000155229 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97461862..97462696 32194978 MeRIP-seq:(Medium) rs367731247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3937977,Human_RBP_ID_4145167 Human_Splice_Rec_1165816,Human_Splice_Rec_1165817,Human_Splice_Rec_1165848,Human_Splice_Rec_1165849,Human_Splice_Rec_1165906,Human_Splice_Rec_1165907,Human_Splice_Rec_1165966,Human_Splice_Rec_1165967,Human_Splice_Rec_1166028,Human_Splice_Rec_1166029,Human_Splice_Rec_1166090,Human_Splice_Rec_1166091,Human_Splice_Rec_1166148,Human_Splice_Rec_1166149,Human_Splice_Rec_1166174,Human_Splice_Rec_1166175 RMVar_hsa_circ_89563,RMVar_hsa_circ_106110,RMVar_hsa_circ_145421,RMVar_hsa_circ_145424,RMVar_hsa_circ_106951,RMVar_hsa_circ_145422,RMVar_hsa_circ_111611,RMVar_hsa_circ_145425,RMVar_hsa_circ_145427,RMVar_hsa_circ_92398,RMVar_hsa_circ_145429,RMVar_hsa_circ_309079,RMVar_hsa_circ_145428,RMVar_hsa_circ_114477,RMVar_hsa_circ_312888,RMVar_hsa_circ_359494,RMVar_hsa_circ_145431,RMVar_hsa_circ_287289,RMVar_hsa_circ_145430,RMVar_hsa_circ_145432,RMVar_hsa_circ_49917 79683 RMVar_ID_79683 Human_SNP_ID_443578135 m1A Human chr10 + 97498147 97498147 97498147 AACTTGTTACGGCTCTGAACCTCGCGGTGCTCACTAACCAGCCTTGAGACCAATCTCTCAAAGTC AACTTGTTACGGCTCTGAACCTCGCGGTGCTCCCTAACCAGCCTTGAGACCAATCTCTCAAAGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97498145..97498256 26863196 MeRIP-seq:(Medium) rs990850860 Functional Loss SNV dbSNP153 33..33 33 - - - 79684 RMVar_ID_79684 Human_SNP_ID_443578570 m1A Human chr10 + 97499040 97499040 97499040 AGTCTGCCACTTCCCTCTCTCCCCTGGCCCGCAAAGTTTTGGCGGAGCCATCGCTGGGGCTGAGC AGTCTGCCACTTCCCTCTCTCCCCTGGCCCGCCAAGTTTTGGCGGAGCCATCGCTGGGGCTGAGC A C UBTD1 Ensembl:ENSG00000165886 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:97498992..97499131 26863196 MeRIP-seq:(Medium) rs1157686750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135979,Human_RBP_ID_8996052 RMVar_hsa_circ_145449,RMVar_hsa_circ_119224 79685 RMVar_ID_79685 Human_SNP_ID_443595363 m1A Human chr10 - 97568006 97568006 97568006 CTTGCGGCCCTCGAAGGCAGGCGCTGTGTCCCAGAACTCATCCCGTTTGCTCCGCAGCTGCCCGT CTTGCGGCCCTCGAAGGCAGGCGCTGTGTCCCGGAACTCATCCCGTTTGCTCCGCAGCTGCCCGT T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:97567959..97568033 26863196 MeRIP-seq:(Medium) rs1474286308 Functional Loss SNV dbSNP153 33..33 33 - - - 79686 RMVar_ID_79686 Human_SNP_ID_443595937 m1A Human chr10 - 97570246 97570246 97570246 GGCGCACGCTGGGTGGAGGCTCGGGGGGCTCCAGGCTCTCCTCCTCCGTGTGCTCCAGCAGCAGG GGCGCACGCTGGGTGGAGGCTCGGGGGGCTCCCGGCTCTCCTCCTCCGTGTGCTCCAGCAGCAGG T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97570136..97570335 26863196 MeRIP-seq:(Medium) rs751301741 Functional Loss SNV dbSNP153 33..33 33 - - - 79687 RMVar_ID_79687 Human_SNP_ID_443596056 m1A Human chr10 + 97570501 97570501 97570501 GAAAGATTTTGTCATCCAGGTCATCATCAACCAGCCCCCACCACCCCAGGACTGATGGGCCCACG GAAAGATTTTGTCATCCAGGTCATCATCAACCGGCCCCCACCACCCCAGGACTGATGGGCCCACG A G UBTD1 Ensembl:ENSG00000165886 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:97570450..97570608 26863196 MeRIP-seq:(Medium) rs1469065087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27408088 RMVar_hsa_circ_145449,RMVar_hsa_circ_119224,RMVar_hsa_circ_145451,RMVar_hsa_circ_103470 79688 RMVar_ID_79688 Human_SNP_ID_443598865 m1A Human chr10 + 97581393 97581393 97581393 GAGGTGGTGAAACTTCTGCAAAGCCATGGAGCAGACACCAATGTGAGGGATAAGGTGAGGCAAAA GAGGTGGTGAAACTTCTGCAAAGCCATGGAGCGGACACCAATGTGAGGGATAAGGTGAGGCAAAA A G ANKRD2 Ensembl:ENSG00000165887 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:97581376..97581468 26863196 MeRIP-seq:(Medium) rs773333184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1166322,Human_Splice_Rec_1166323,Human_Splice_Rec_1166338,Human_Splice_Rec_1166339,Human_Splice_Rec_1166352,Human_Splice_Rec_1166353,Human_Splice_Rec_1166368,Human_Splice_Rec_1166369 79689 RMVar_ID_79689 Human_SNP_ID_443613971 m1A Human chr10 + 97640760 97640760 97640760 CCGGCTGTCTGAGGGATGGACGAGACGAGCCCACTAGTGTCCCCCGAGCGGGCCCAACCCCCGGA CCGGCTGTCTGAGGGATGGACGAGACGAGCCCGCTAGTGTCCCCCGAGCGGGCCCAACCCCCGGA A G PI4K2A,AL355315.1 Ensembl:ENSG00000155252,Ensembl:ENSG00000249967 Protein coding,Protein coding CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:97640713..97640885 26863196 MeRIP-seq:(Medium) rs1232701406 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 79690 RMVar_ID_79690 Human_SNP_ID_443622718 m1A Human chr10 - 97677905 97677905 97677905 AGTGCCAGGATCCGCCGGAACTGGAGGAAGTCAGGCCCCACAAGCTACCTCCACCAGATCAGACA AGTGCCAGGATCCGCCGGAACTGGAGGAAGTCGGGCCCCACAAGCTACCTCCACCAGATCAGACA T C AVPI1 Ensembl:ENSG00000119986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:97677854..97678050 26863196 MeRIP-seq:(Medium) rs1393677128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1914295,Human_miRNA_ID_1921652,Human_miRNA_ID_1924108,Human_miRNA_ID_1931463,Human_miRNA_ID_2629292,Human_miRNA_ID_3125144 RMVar_hsa_circ_90180,RMVar_hsa_circ_119156,RMVar_hsa_circ_145461,RMVar_hsa_circ_145462 79691 RMVar_ID_79691 Human_SNP_ID_443623441 m1A Human chr10 - 97679720 97679720 97679720 GAGGAACGGGCACAGATCATCTGGGAATGTGCAGGGGACCACCGTGTGGCTGAGGCCCTCAAGAG GAGGAACGGGCACAGATCATCTGGGAATGTGCGGGGGACCACCGTGTGGCTGAGGCCCTCAAGAG T C AVPI1 Ensembl:ENSG00000119986 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97679670..97679853 26863196 MeRIP-seq:(Medium) rs759274301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18970203 RMVar_hsa_circ_105774,RMVar_hsa_circ_90180,RMVar_hsa_circ_119156,RMVar_hsa_circ_145461,RMVar_hsa_circ_145462,RMVar_hsa_circ_145463 79692 RMVar_ID_79692 Human_SNP_ID_443631685 m1A Human chr10 + 97713536 97713511 97713536 GGACGAAGGAATCCGAGCTGGGGGCCTGGCGCAGAGGGGAAAGGGGGGCGCCAGGGTGGTGAGCG GGACGAAG_________________________GAGGGGAAAGGGGGGCGCCAGGGTGGTGAGCG GGAATCCGAGCTGGGGGCCTGGCGCA G MARVELD1 Ensembl:ENSG00000155254 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97713485..97713591 26863196 MeRIP-seq:(Medium) rs1243114723 Functional Loss DEL dbSNP153 9..33 33 - - - Human_Splice_Rec_1166459 79693 RMVar_ID_79693 Human_SNP_ID_443631890 m1A Human chr10 + 97714040 97714040 97714040 CTTCTGGATCACTATCGCCACCAGCAAGTACCAGGGCCCCGTGCACTTCGCGCTCTTCGTGTCCG CTTCTGGATCACTATCGCCACCAGCAAGTACCGGGGCCCCGTGCACTTCGCGCTCTTCGTGTCCG A G MARVELD1 Ensembl:ENSG00000155254 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:97713796..97714050 26863196 MeRIP-seq:(Medium) rs1317090802 Functional Loss SNV dbSNP153 33..33 33 - - - 79694 RMVar_ID_79694 Human_SNP_ID_443631900 m1A Human chr10 - 97714061 97714061 97714061 GGGTGAGCAGCCAGAAGAGCACGGACACGAAGAGCGCGAAGTGCACGGGGCCCTGGTACTTGCTG GGGTGAGCAGCCAGAAGAGCACGGACACGAAGGGCGCGAAGTGCACGGGGCCCTGGTACTTGCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:97713726..97714187 26863196 MeRIP-seq:(Medium) rs896960347 Functional Loss SNV dbSNP153 33..33 33 - - - 79695 RMVar_ID_79695 Human_SNP_ID_443631971 m1A Human chr10 - 97714220 97714220 97714220 AGTAGCTGTGGCGCTGCATCTGGTCGCTCATGATGCCGGTGGCGGCGCCGTAGAGCGCGGCCGCC AGTAGCTGTGGCGCTGCATCTGGTCGCTCATGGTGCCGGTGGCGGCGCCGTAGAGCGCGGCCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:97714170..97714320 26863196 MeRIP-seq:(Medium) rs1419687206 Functional Loss SNV dbSNP153 33..33 33 - - - 79696 RMVar_ID_79696 Human_SNP_ID_443632086 m1A Human chr10 + 97714550 97714550 97714550 TCCAGCGTTTCCACTGTCGCCCGCGCCCGGGAACCCTGACGCTCAGCTCCCGCCCGACGGCAGCG TCCAGCGTTTCCACTGTCGCCCGCGCCCGGGACCCCTGACGCTCAGCTCCCGCCCGACGGCAGCG A C MARVELD1 Ensembl:ENSG00000155254 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97714501..97714762 26863196 MeRIP-seq:(Medium) rs576317560 Functional Loss SNV dbSNP153 33..33 33 - - - 79697 RMVar_ID_79697 Human_SNP_ID_443637859 m1A Human chr10 + 97737217 97737217 97737217 ACCTGCGACTTCCGAACAACCCTGGCAGGAGGAGCGGCGTTCAGCCGGGGGAGGCCTGAAGAAAC ACCTGCGACTTCCGAACAACCCTGGCAGGAGGTGCGGCGTTCAGCCGGGGGAGGCCTGAAGAAAC A T ZFYVE27 Ensembl:ENSG00000155256 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:97737170..97737274;chr10:97737172..97737272 26863196 MeRIP-seq:(Medium) rs565425611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5435866 79698 RMVar_ID_79698 Human_SNP_ID_443638193 m1A Human chr10 - 97738530 97738530 97738530 GAAAAGGTGGAGACTCCAGGGGAGCCTCGGGCATCACGCTGGGGCTCAGCTCCGGCCCACTCCCC GAAAAGGTGGAGACTCCAGGGGAGCCTCGGGCGTCACGCTGGGGCTCAGCTCCGGCCCACTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:97738433..97738544;chr10:97738426..97738535 26863196 MeRIP-seq:(Medium) rs769322350 Functional Loss SNV dbSNP153 33..33 33 - - - 79699 RMVar_ID_79699 Human_SNP_ID_443639709 m1A Human chr10 + 97744519 97744519 97744519 CTTCATTAGAGGAGACAACAGACATGCCTGCAATGTGTCATGTGGTGATAAGGTCTATGAGGAAT CTTCATTAGAGGAGACAACAGACATGCCTGCAGTGTGTCATGTGGTGATAAGGTCTATGAGGAAT A G ZFYVE27 Ensembl:ENSG00000155256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:97744468..97744655 26863196 MeRIP-seq:(Medium) rs950195435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23480753 RMVar_hsa_circ_44792,RMVar_hsa_circ_304079,RMVar_hsa_circ_309446,RMVar_hsa_circ_60867,RMVar_hsa_circ_145465,RMVar_hsa_circ_145466 79700 RMVar_ID_79700 Human_SNP_ID_443641691 m1A Human chr10 + 97751437 97751437 97751437 CAGCGTGGAGGAGGCTGAGGAGGCTGAGCCAGATGAAGAGTTTAAAGATGCGATTGAGGTGGGTG CAGCGTGGAGGAGGCTGAGGAGGCTGAGCCAGTTGAAGAGTTTAAAGATGCGATTGAGGTGGGTG A T ZFYVE27 Ensembl:ENSG00000155256 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:97750411..97753110 26863196 MeRIP-seq:(Medium) rs1288998809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862666,Human_RBP_ID_5545991,Human_RBP_ID_18970206,Human_RBP_ID_22753164,Human_RBP_ID_26316559 Human_Splice_Rec_1166482,Human_Splice_Rec_1166483,Human_Splice_Rec_1166498,Human_Splice_Rec_1166499,Human_Splice_Rec_1166516,Human_Splice_Rec_1166517,Human_Splice_Rec_1166534,Human_Splice_Rec_1166535,Human_Splice_Rec_1166556,Human_Splice_Rec_1166557,Human_Splice_Rec_1166580,Human_Splice_Rec_1166581,Human_Splice_Rec_1166604,Human_Splice_Rec_1166605,Human_Splice_Rec_1166616 RMVar_hsa_circ_96705,RMVar_hsa_circ_44792,RMVar_hsa_circ_60867,RMVar_hsa_circ_51312,RMVar_hsa_circ_103725,RMVar_hsa_circ_145468,RMVar_hsa_circ_145470,RMVar_hsa_circ_91063,RMVar_hsa_circ_145469 79701 RMVar_ID_79701 Human_SNP_ID_443643211 m1A Human chr10 + 97757343 97757343 97757343 GGTGAGTGTCTGTGAGGGTGCATTTGTTGGGGACAGTGTCCTTGGGACTGTCGGGTGGGGAGGAG GGTGAGTGTCTGTGAGGGTGCATTTGTTGGGGGCAGTGTCCTTGGGACTGTCGGGTGGGGAGGAG A G ZFYVE27 Ensembl:ENSG00000155256 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:97757292..97757450 26863196 MeRIP-seq:(Medium) rs770981071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23480790 Human_Splice_Rec_1166486,Human_Splice_Rec_1166502,Human_Splice_Rec_1166520,Human_Splice_Rec_1166538,Human_Splice_Rec_1166562,Human_Splice_Rec_1166586,Human_Splice_Rec_1166608 79702 RMVar_ID_79702 Human_SNP_ID_443733787 m1A Human chr10 - 98134708 98134708 98134708 GTACAGAGGGAGGGGATACGGGGCTGGTTGTTACCGGCGCGCTGTTGCTCTCCGCTTCCGCCGTC GTACAGAGGGAGGGGATACGGGGCTGGTTGTTGCCGGCGCGCTGTTGCTCTCCGCTTCCGCCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:98134685..98134758;chr10:98134681..98134769 26863196 MeRIP-seq:(Medium) rs913427201 Functional Loss SNV dbSNP153 33..33 33 - - - 79703 RMVar_ID_79703 Human_SNP_ID_443798878 m1A Human chr10 + 98393820 98393820 98393820 CTCTTAGGATAATGGCCAGTCTTCTAGCAGGCACTCCAGCCTCATCCCTCATCCTGTCCCCCTAT CTCTTAGGATAATGGCCAGTCTTCTAGCAGGCCCTCCAGCCTCATCCCTCATCCTGTCCCCCTAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:98393205..98394138 26863196 MeRIP-seq:(Medium) rs577273037 Functional Loss SNV dbSNP153 33..33 33 - - - 79704 RMVar_ID_79704 Human_SNP_ID_443804337 m1A Human chr10 - 98415016 98415016 98415016 GGTCTGAAGCCTGAGTATGATGCGGTGGTGATAGGAGCAGGTAAAGTGGTAAAGCAGGCCGGGCC GGTCTGAAGCCTGAGTATGATGCGGTGGTGATTGGAGCAGGTAAAGTGGTAAAGCAGGCCGGGCC T A PYROXD2 Ensembl:ENSG00000119943 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:98415013..98415120 26863196 MeRIP-seq:(Medium) rs768519902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1166899,Human_Splice_Rec_1166933,Human_Splice_Rec_1166937 RMVar_hsa_circ_84018,RMVar_hsa_circ_82500,RMVar_hsa_circ_145497,RMVar_hsa_circ_145498 79705 RMVar_ID_79705 Human_SNP_ID_443804338 m1A Human chr10 - 98415016 98415016 98415016 GGTCTGAAGCCTGAGTATGATGCGGTGGTGATAGGAGCAGGTAAAGTGGTAAAGCAGGCCGGGCC GGTCTGAAGCCTGAGTATGATGCGGTGGTGATGGGAGCAGGTAAAGTGGTAAAGCAGGCCGGGCC T C PYROXD2 Ensembl:ENSG00000119943 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:98415013..98415120 26863196 MeRIP-seq:(Medium) rs768519902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1166899,Human_Splice_Rec_1166933,Human_Splice_Rec_1166937 RMVar_hsa_circ_84018,RMVar_hsa_circ_82500,RMVar_hsa_circ_145497,RMVar_hsa_circ_145498 79706 RMVar_ID_79706 Human_SNP_ID_443804976 m1A Human chr10 + 98417250 98417250 98417250 GCTGGGTGGGCTTCCTCCACGCAGGGAACAGCAGAGATGGGGCTTCCTCCCCATCTCCCAGGATA GCTGGGTGGGCTTCCTCCACGCAGGGAACAGCGGAGATGGGGCTTCCTCCCCATCTCCCAGGATA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:98417200..98417337 32194978 MeRIP-seq:(Medium) rs1335543774 Functional Loss SNV dbSNP153 33..33 33 - - - 79707 RMVar_ID_79707 Human_SNP_ID_444018276 m1A Human chr10 + 99329642 99329642 99329642 TATTTCCAGCCAGGACCGCCGGCCACCGCCGCACCGGTGCCCTCACCGACCCTCAACTCGGGGGA TATTTCCAGCCAGGACCGCCGGCCACCGCCGCGCCGGTGCCCTCACCGACCCTCAACTCGGGGGA A G CNNM1 Ensembl:ENSG00000119946 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:99329558..99329795 26863196 MeRIP-seq:(Medium) rs1486372263 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5520211,Human_RBP_ID_18584502 79708 RMVar_ID_79708 Human_SNP_ID_444035195 m1A Human chr10 - 99402598 99402598 99402598 GGAACCACATCACTGATCAAATTGGCATGTTCAGCTTCACTGGGTTGAACCGTAAGTGGCCCCCA GGAACCACATCACTGATCAAATTGGCATGTTCGGCTTCACTGGGTTGAACCGTAAGTGGCCCCCA T C GOT1 Ensembl:ENSG00000120053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:99397611..99402604 32194978 MeRIP-seq:(Medium) rs771467913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17224986,Human_RBP_ID_17457065,Human_RBP_ID_18970212,Human_RBP_ID_22432582 Human_Splice_Rec_1167341,Human_Splice_Rec_1167345 RMVar_hsa_circ_82415,RMVar_hsa_circ_125378,RMVar_hsa_circ_102915,RMVar_hsa_circ_145508,RMVar_hsa_circ_145509,RMVar_hsa_circ_145510,RMVar_hsa_circ_37758 79709 RMVar_ID_79709 Human_SNP_ID_444035204 m1A Human chr10 - 99402646 99402646 99402646 GATCTGAACTCAGGGCACGACTAGAAGCCCTCAAAACCCCTGGGACCTGGAACCACATCACTGAT GATCTGAACTCAGGGCACGACTAGAAGCCCTCGAAACCCCTGGGACCTGGAACCACATCACTGAT T C GOT1 Ensembl:ENSG00000120053 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs760981253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3335783,Human_RBP_ID_17229472,Human_RBP_ID_17457065,Human_RBP_ID_22431559 Human_Splice_Rec_1167340,Human_Splice_Rec_1167341,Human_Splice_Rec_1167344,Human_Splice_Rec_1167345 RMVar_hsa_circ_82415,RMVar_hsa_circ_125378,RMVar_hsa_circ_102915,RMVar_hsa_circ_145508,RMVar_hsa_circ_145509,RMVar_hsa_circ_145510,RMVar_hsa_circ_37758 79710 RMVar_ID_79710 Human_SNP_ID_444088240 m1A Human chr10 + 99620226 99620226 99620226 CCCCGGCCTCCCCGCCGCCGGCCCCCCGGCCCACGCCCCGCTGCAGCCACCCGTCCAGCAGCGCC CCCCGGCCTCCCCGCCGCCGGCCCCCCGGCCCCCGCCCCGCTGCAGCCACCCGTCCAGCAGCGCC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:99620140..99620388 26863410 MeRIP-seq:(Medium) rs1377538215 Functional Loss SNV dbSNP153 33..33 33 - - - 79711 RMVar_ID_79711 Human_SNP_ID_444088284 m1A Human chr10 - 99620350 99620350 99620350 GTGGTGGCAGCGGCGGCGGGGGTGGGCGCCGCAGCTGGCCCGGGTGGATGGAGTTGGAGGGGCGG GTGGTGGCAGCGGCGGCGGGGGTGGGCGCCGCGGCTGGCCCGGGTGGATGGAGTTGGAGGGGCGG T C SLC25A28 Ensembl:ENSG00000155287 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:99620073..99620451 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_259141,Human_RBP_ID_3364792,Human_RBP_ID_4135986,Human_RBP_ID_8172281,Human_RBP_ID_8228693,Human_RBP_ID_9352565,Human_RBP_ID_9413154,Human_RBP_ID_18416323,Human_RBP_ID_18931152,Human_RBP_ID_26317394,Human_RBP_ID_26767716 79712 RMVar_ID_79712 Human_SNP_ID_444088285 m1A Human chr10 - 99620350 99620350 99620350 GTGGTGGCAGCGGCGGCGGGGGTGGGCGCCGCAGCTGGCCCGGGTGGATGGAGTTGGAGGGGCGG GTGGTGGCAGCGGCGGCGGGGGTGGGCGCCGCCGCTGGCCCGGGTGGATGGAGTTGGAGGGGCGG T G SLC25A28 Ensembl:ENSG00000155287 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:99620073..99620451 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_259141,Human_RBP_ID_3364792,Human_RBP_ID_4135986,Human_RBP_ID_8172281,Human_RBP_ID_8228693,Human_RBP_ID_9352565,Human_RBP_ID_9413154,Human_RBP_ID_18416323,Human_RBP_ID_18931152,Human_RBP_ID_26317394,Human_RBP_ID_26767716 79713 RMVar_ID_79713 Human_SNP_ID_444088294 m1A Human chr10 - 99620374 99620371 99620374 CGGGGCCGGGGGGCGGCGGCGGCAGTGGTGGCAGCGGCGGCGGGGGTGGGCGCCGCAGCTGGCCC CGGGGCCGGGGGGCGGCGGCGGCAGTGGTGGC___GGCGGCGGGGGTGGGCGCCGCAGCTGGCCC CGCT C SLC25A28 Ensembl:ENSG00000155287 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:99620050..99620560 26863196 MeRIP-seq:(Medium) rs1194720026 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8228693,Human_RBP_ID_9352565,Human_RBP_ID_9413154,Human_RBP_ID_18416323 79714 RMVar_ID_79714 Human_SNP_ID_444097365 m1A Human chr10 + 99659567 99659567 99659567 CAGCTCGGGACTGAACCGAGAGGTGCCGAAGGAACCGGCGGGCCGCTTGATCCCGTGAGTGTGGG CAGCTCGGGACTGAACCGAGAGGTGCCGAAGGCACCGGCGGGCCGCTTGATCCCGTGAGTGTGGG A C ENTPD7 Ensembl:ENSG00000198018 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:99659524..99659648 26863196 MeRIP-seq:(Medium) rs1319743635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135987,Human_RBP_ID_18971068 Human_Splice_Rec_1167459 RMVar_hsa_circ_114388,RMVar_hsa_circ_145513 79715 RMVar_ID_79715 Human_SNP_ID_444097366 m1A Human chr10 + 99659568 99659568 99659568 AGCTCGGGACTGAACCGAGAGGTGCCGAAGGAACCGGCGGGCCGCTTGATCCCGTGAGTGTGGGC AGCTCGGGACTGAACCGAGAGGTGCCGAAGGAGCCGGCGGGCCGCTTGATCCCGTGAGTGTGGGC A G ENTPD7 Ensembl:ENSG00000198018 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:99659519..99659927 26863196 MeRIP-seq:(Medium) rs536057093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135987,Human_RBP_ID_18971068 Human_Splice_Rec_1167459 RMVar_hsa_circ_114388,RMVar_hsa_circ_145513 79716 RMVar_ID_79716 Human_SNP_ID_444113119 m1A Human chr10 - 99732055 99732055 99732055 CTGGGTTGTGGAAGAGGTGGCTGTTCCCTGTCATCAGTATGCAGCGATTGCTCTTTCCGCCGTTG CTGGGTTGTGGAAGAGGTGGCTGTTCCCTGTCTTCAGTATGCAGCGATTGCTCTTTCCGCCGTTG T A COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:99732005..99732080;chr10:99732005..99732070 26863196 MeRIP-seq:(Medium) rs1358306766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367494,Human_RBP_ID_980923,Human_RBP_ID_4136458,Human_RBP_ID_23427432 Human_Splice_Rec_1167435,Human_Splice_Rec_1167539,Human_Splice_Rec_1167555 79717 RMVar_ID_79717 Human_SNP_ID_444113120 m1A Human chr10 - 99732055 99732055 99732055 CTGGGTTGTGGAAGAGGTGGCTGTTCCCTGTCATCAGTATGCAGCGATTGCTCTTTCCGCCGTTG CTGGGTTGTGGAAGAGGTGGCTGTTCCCTGTCCTCAGTATGCAGCGATTGCTCTTTCCGCCGTTG T G COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:99732005..99732080;chr10:99732005..99732070 26863196 MeRIP-seq:(Medium) rs1358306766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367494,Human_RBP_ID_980923,Human_RBP_ID_4136458,Human_RBP_ID_23427432 Human_Splice_Rec_1167435,Human_Splice_Rec_1167539,Human_Splice_Rec_1167555 79718 RMVar_ID_79718 Human_SNP_ID_444113277 m1A Human chr10 + 99732359 99732359 99732359 ACGAGGGAGGAACGCGTGGAGCATGAAAAGGCAGGGGGCCTCCTCTGAGCGAAAACGAGCGCGGA ACGAGGGAGGAACGCGTGGAGCATGAAAAGGCGGGGGGCCTCCTCTGAGCGAAAACGAGCGCGGA A G CUTC Ensembl:ENSG00000119929 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:99732254..99732469;chr10:99732251..99732481 26863196 MeRIP-seq:(Medium) rs1200476381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_806027,Human_RBP_ID_4101000,Human_RBP_ID_23427434 Human_Splice_Rec_1167495,Human_Splice_Rec_1167511 RMVar_hsa_circ_101680,RMVar_hsa_circ_145520 79719 RMVar_ID_79719 Human_SNP_ID_444127701 m1A Human chr10 - 99795052 99795052 99795052 ATTTCACCCCTTACCCTCCAAACCTGCCTCCAAATTTTTCCTTTCCTGTCCTACTGCCTCCTTTC ATTTCACCCCTTACCCTCCAAACCTGCCTCCATATTTTTCCTTTCCTGTCCTACTGCCTCCTTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:99794943..99795123 26863196 MeRIP-seq:(Medium) rs145919603 Functional Loss SNV dbSNP153 33..33 33 - - - 79720 RMVar_ID_79720 Human_SNP_ID_444127702 m1A Human chr10 - 99795052 99795052 99795052 ATTTCACCCCTTACCCTCCAAACCTGCCTCCAAATTTTTCCTTTCCTGTCCTACTGCCTCCTTTC ATTTCACCCCTTACCCTCCAAACCTGCCTCCAGATTTTTCCTTTCCTGTCCTACTGCCTCCTTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:99794943..99795123 26863196 MeRIP-seq:(Medium) rs145919603 Functional Loss SNV dbSNP153 33..33 33 - - - 79721 RMVar_ID_79721 Human_SNP_ID_444150077 m1A Human chr10 + 99880190 99880190 99880190 TCTGGCAAGACCCCGAGGTAAAGGATACAGCCATGCTGCTGGGGTTGAAGGTCAGGGTGCTGCCG TCTGGCAAGACCCCGAGGTAAAGGATACAGCCGTGCTGCTGGGGTTGAAGGTCAGGGTGCTGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:99880140..99880230 26863196 MeRIP-seq:(Medium) rs780739840 Functional Loss SNV dbSNP153 33..33 33 - - - 79722 RMVar_ID_79722 Human_SNP_ID_444150145 m1A Human chr10 - 99880322 99880322 99880322 AGGCTTCGTGTACAGCTCTTTCCTAAAGCCCTACAATCCTCGCCGCAGCCACTCCGATGCCTCCG AGGCTTCGTGTACAGCTCTTTCCTAAAGCCCTGCAATCCTCGCCGCAGCCACTCCGATGCCTCCG T C DNMBP Ensembl:ENSG00000107554 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:99880026..99880350 26863196 MeRIP-seq:(Medium) rs946191245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17225038 Human_Splice_Rec_1167758,Human_Splice_Rec_1167784,Human_Splice_Rec_1167816 Human_miRNA_ID_2766714 RMVar_hsa_circ_39450,RMVar_hsa_circ_115703,RMVar_hsa_circ_312438,RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_145581 79723 RMVar_ID_79723 Human_SNP_ID_444150146 m1A Human chr10 - 99880322 99880322 99880322 AGGCTTCGTGTACAGCTCTTTCCTAAAGCCCTACAATCCTCGCCGCAGCCACTCCGATGCCTCCG AGGCTTCGTGTACAGCTCTTTCCTAAAGCCCTCCAATCCTCGCCGCAGCCACTCCGATGCCTCCG T G DNMBP Ensembl:ENSG00000107554 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:99880026..99880350 26863196 MeRIP-seq:(Medium) rs946191245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17225038 Human_Splice_Rec_1167758,Human_Splice_Rec_1167784,Human_Splice_Rec_1167816 Human_miRNA_ID_2766714 RMVar_hsa_circ_39450,RMVar_hsa_circ_115703,RMVar_hsa_circ_312438,RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_145581 79724 RMVar_ID_79724 Human_SNP_ID_444161697 m1A Human chr10 - 99923742 99923742 99923742 GAGAAGCAAGGAGAACAGTTCTGGTTGGGGAAACTATGAGAAAGACATAGGGTTGTGGTGACAAA GAGAAGCAAGGAGAACAGTTCTGGTTGGGGAATCTATGAGAAAGACATAGGGTTGTGGTGACAAA T A DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:99923694..99923789 26863196 MeRIP-seq:(Medium) rs970422227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51010 79725 RMVar_ID_79725 Human_SNP_ID_444169601 m1A Human chr10 - 99956837 99956837 99956837 TGGGGCCCCTGAGGACTGTGGATGAGTCAGTAAGTTCTGGAAATCAAGATGACTGCATTGTTAAT TGGGGCCCCTGAGGACTGTGGATGAGTCAGTAGGTTCTGGAAATCAAGATGACTGCATTGTTAAT T C DNMBP Ensembl:ENSG00000107554 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:99956786..99956912 26863196 MeRIP-seq:(Medium) rs1304130223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28622,Human_RBP_ID_5520244,Human_RBP_ID_8323465,Human_RBP_ID_18584622 RMVar_hsa_circ_51010,RMVar_hsa_circ_317362,RMVar_hsa_circ_338604 79726 RMVar_ID_79726 Human_SNP_ID_444215379 m1A Human chr10 - 100152035 100152029 100152035 TTATACGGACTCTTCAGATTTACAGAGAACTTACACTTCATCTGTTCCACCTCTCCTGCGATAGT TTATACGGACTCTTCAGATTTACAGAGAACTT______CATCTGTTCCACCTCTCCTGCGATAGT GAAGTGT G ERLIN1 Ensembl:ENSG00000107566 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100151990..100152141 32194978 MeRIP-seq:(Medium) rs1292164800 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_746903,Human_RBP_ID_17225046,Human_RBP_ID_17462161,Human_RBP_ID_17767319 RMVar_hsa_circ_83645,RMVar_hsa_circ_145595 79727 RMVar_ID_79727 Human_SNP_ID_444225998 m1A Human chr10 - 100199688 100199688 100199688 GAAGACAGAAAAAAGGAACTCAGAGAGGAAAAAGCAGCAAGAAAATGTTTAGAAAGATGGAAAAA GAAGACAGAAAAAAGGAACTCAGAGAGGAAAAGGCAGCAAGAAAATGTTTAGAAAGATGGAAAAA T C CHUK Ensembl:ENSG00000213341 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:100199637..100199751 26863196 MeRIP-seq:(Medium) rs1171206848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863813 RMVar_hsa_circ_190,RMVar_hsa_circ_61604,RMVar_hsa_circ_296626,RMVar_hsa_circ_302900,RMVar_hsa_circ_9313,RMVar_hsa_circ_70371,RMVar_hsa_circ_145602,RMVar_hsa_circ_145603,RMVar_hsa_circ_61220,RMVar_hsa_circ_83919,RMVar_hsa_circ_145604,RMVar_hsa_circ_105737,RMVar_hsa_circ_145605,RMVar_hsa_circ_15033 79728 RMVar_ID_79728 Human_SNP_ID_444233526 m1A Human chr10 - 100233026 100233026 100233026 CTCCCACCTCAGCCTCATGAGTAGCTGGGACCACAGGCGCATGCTACCATGCCTGGCAAACTTTT CTCCCACCTCAGCCTCATGAGTAGCTGGGACCGCAGGCGCATGCTACCATGCCTGGCAAACTTTT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3190709 Functional Loss SNV dbSNP153 33..33 33 - - - 79729 RMVar_ID_79729 Human_SNP_ID_444241973 m1A Human chr10 + 100267545 100267545 100267545 GTCACCTACACACACGAAAGAGACACAGGGAGAGAGGCTTCCATTCACGGTCACTCACAGGCGCA GTCACCTACACACACGAAAGAGACACAGGGAGCGAGGCTTCCATTCACGGTCACTCACAGGCGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100267496..100267585 26863196 MeRIP-seq:(Medium) rs1392822577 Functional Loss SNV dbSNP153 33..33 33 - - - 79730 RMVar_ID_79730 Human_SNP_ID_444247150 m1A Human chr10 + 100286209 100286209 100286209 TCCTTTGCTTCCTCAGCTGTCTCCACGGCGGCATCGTCTGGGCCAAGGGAGAATGACTAAGTGTC TCCTTTGCTTCCTCAGCTGTCTCCACGGCGGCGTCGTCTGGGCCAAGGGAGAATGACTAAGTGTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100282926..100286237 32194978 MeRIP-seq:(Medium) rs1293064369 Functional Loss SNV dbSNP153 33..33 33 - - - 79731 RMVar_ID_79731 Human_SNP_ID_444247351 m1A Human chr10 - 100286659 100286659 100286659 CACCCCGGCCCGGAAACAGCGCGGGGTCCGCTATGGCGGCGGCAGCCGAGGGCGTACTGGCGACC CACCCCGGCCCGGAAACAGCGCGGGGTCCGCTTTGGCGGCGGCAGCCGAGGGCGTACTGGCGACC T A BLOC1S2 Ensembl:ENSG00000196072 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:100286542..100286661 26863196 MeRIP-seq:(Medium) rs1250777403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367702,Human_RBP_ID_4136465,Human_RBP_ID_8981231 Human_Splice_Rec_1168131,Human_Splice_Rec_1168149 79732 RMVar_ID_79732 Human_SNP_ID_444262876 m1A Human chr10 - 100347240 100347238 100347241 TATCCGCTGCCAAGCAGGGGCAAAGTGCGAGGAGTTGACTGGCGCGGGCGGTCCCGCGTGGAGGT TATCCGCTGCCAAGCAGGGGCAAAGTGCGAG___TTGACTGGCGCGGGCGGTCCCGCGTGGAGGT ACTC A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:100347142..100347239 26863410 MeRIP-seq:(Medium) rs370836642 Functional Loss DEL dbSNP153 32..34 33 - - - 79733 RMVar_ID_79733 Human_SNP_ID_444262878 m1A Human chr10 - 100347240 100347240 100347240 TATCCGCTGCCAAGCAGGGGCAAAGTGCGAGGAGTTGACTGGCGCGGGCGGTCCCGCGTGGAGGT TATCCGCTGCCAAGCAGGGGCAAAGTGCGAGGGGTTGACTGGCGCGGGCGGTCCCGCGTGGAGGT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:100347142..100347239 26863410 MeRIP-seq:(Medium) rs199535276 Functional Loss SNV dbSNP153 33..33 33 - - - 79734 RMVar_ID_79734 Human_SNP_ID_444262879 m1A Human chr10 - 100347240 100347240 100347240 TATCCGCTGCCAAGCAGGGGCAAAGTGCGAGGAGTTGACTGGCGCGGGCGGTCCCGCGTGGAGGT TATCCGCTGCCAAGCAGGGGCAAAGTGCGAGGCGTTGACTGGCGCGGGCGGTCCCGCGTGGAGGT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:100347142..100347239 26863410 MeRIP-seq:(Medium) rs199535276 Functional Loss SNV dbSNP153 33..33 33 - - - 79735 RMVar_ID_79735 Human_SNP_ID_444262884 m1A Human chr10 + 100347247 100347247 100347247 CGCGGGACCGCCCGCGCCAGTCAACTCCTCGCACTTTGCCCCTGCTTGGCAGCGGATAAAAGGGG CGCGGGACCGCCCGCGCCAGTCAACTCCTCGCCCTTTGCCCCTGCTTGGCAGCGGATAAAAGGGG A C SCD Ensembl:ENSG00000099194 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:100347126..100347550 26863196 MeRIP-seq:(Medium) rs1051873179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26506,Human_RBP_ID_273481,Human_RBP_ID_291784,Human_RBP_ID_367704,Human_RBP_ID_1439957,Human_RBP_ID_3336084,Human_RBP_ID_4135997,Human_RBP_ID_5414593,Human_RBP_ID_5434820,Human_RBP_ID_5458697,Human_RBP_ID_8323616,Human_RBP_ID_8756599,Human_RBP_ID_9254155,Human_RBP_ID_17345746,Human_RBP_ID_18931784,Human_RBP_ID_19577493,Human_RBP_ID_22532235,Human_RBP_ID_26872841,Human_RBP_ID_27403100 Human_miRNA_ID_384185,Human_miRNA_ID_560728,Human_miRNA_ID_568191,Human_miRNA_ID_768916,Human_miRNA_ID_1598007,Human_miRNA_ID_1942556,Human_miRNA_ID_1945600,Human_miRNA_ID_2116747,Human_miRNA_ID_2200322,Human_miRNA_ID_2203388,Human_miRNA_ID_2815847,Human_miRNA_ID_2845980,Human_miRNA_ID_2849004,Human_miRNA_ID_2863111,Human_miRNA_ID_3112839 RMVar_hsa_circ_85923,RMVar_hsa_circ_145624 79736 RMVar_ID_79736 Human_SNP_ID_444262940 m1A Human chr10 + 100347449 100347449 100347449 GCTTCGAAACCGCAGTCCTCCGGCGACCCCGAACTCCGCTCCGGAGCCTCAGCCCCCTGGAAAGT GCTTCGAAACCGCAGTCCTCCGGCGACCCCGACCTCCGCTCCGGAGCCTCAGCCCCCTGGAAAGT A C SCD Ensembl:ENSG00000099194 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:100347131..100348150;chr10:100347131..100348175;chr10:100347126..100347550;chr10:100347101..100347531 26863196 MeRIP-seq:(Medium) rs1180140864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225060,Human_RBP_ID_747124,Human_RBP_ID_805835,Human_RBP_ID_864279,Human_RBP_ID_1439962,Human_RBP_ID_1758320,Human_RBP_ID_3336085,Human_RBP_ID_4101446,Human_RBP_ID_5414597,Human_RBP_ID_5434824,Human_RBP_ID_9320677,Human_RBP_ID_18187988,Human_RBP_ID_22431566,Human_RBP_ID_22532213,Human_RBP_ID_26391604,Human_RBP_ID_26802885,Human_RBP_ID_26872845 Human_Splice_Rec_1168225 RMVar_hsa_circ_85923,RMVar_hsa_circ_145624 79737 RMVar_ID_79737 Human_SNP_ID_444262944 m1A Human chr10 - 100347456 100347456 100347456 CGGGATCACTTTCCAGGGGGCTGAGGCTCCGGAGCGGAGTTCGGGGTCGCCGGAGGACTGCGGTT CGGGATCACTTTCCAGGGGGCTGAGGCTCCGGGGCGGAGTTCGGGGTCGCCGGAGGACTGCGGTT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:100347101..100347575 26863410 MeRIP-seq:(Medium) rs1279001494 Functional Loss SNV dbSNP153 33..33 33 - - - 79738 RMVar_ID_79738 Human_SNP_ID_444262975 m1A Human chr10 - 100347531 100347531 100347531 CCGGCGGTACGGGGCCAGGCTGGGAAACTCACATCGTCCTGCAGCAAGTGGGCCGGCATCTTGGC CCGGCGGTACGGGGCCAGGCTGGGAAACTCACCTCGTCCTGCAGCAAGTGGGCCGGCATCTTGGC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:100347526..100347550 26863196 MeRIP-seq:(Medium) rs761702537 Functional Loss SNV dbSNP153 33..33 33 - - - 79739 RMVar_ID_79739 Human_SNP_ID_444263161 m1A Human chr10 + 100348132 100348132 100348132 GCGCCTCCCTCCAGGGTCCTGCAGAATGGAGGAGATAAGTTGGAGACGATGCCCCTCTACTTGGA GCGCCTCCCTCCAGGGTCCTGCAGAATGGAGGTGATAAGTTGGAGACGATGCCCCTCTACTTGGA A T SCD Ensembl:ENSG00000099194 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:100348048..100348230;chr10:100348046..100348157;chr10:100348082..100348177 26863196 MeRIP-seq:(Medium) rs746829852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26509,Human_RBP_ID_367708,Human_RBP_ID_747126,Human_RBP_ID_805836,Human_RBP_ID_864281,Human_RBP_ID_1439964,Human_RBP_ID_4136004,Human_RBP_ID_5915793,Human_RBP_ID_9568391,Human_RBP_ID_17225068,Human_RBP_ID_18187989,Human_RBP_ID_19452028,Human_RBP_ID_22431839,Human_RBP_ID_22787056,Human_RBP_ID_24772331,Human_RBP_ID_26872852 Human_Splice_Rec_1168226 Human_miRNA_ID_1538867,Human_miRNA_ID_1593067,Human_miRNA_ID_2789296,Human_miRNA_ID_2818908 RMVar_hsa_circ_85923,RMVar_hsa_circ_46856,RMVar_hsa_circ_145624 79740 RMVar_ID_79740 Human_SNP_ID_444263162 m1A Human chr10 + 100348134 100348134 100348134 GCCTCCCTCCAGGGTCCTGCAGAATGGAGGAGATAAGTTGGAGACGATGCCCCTCTACTTGGAAG GCCTCCCTCCAGGGTCCTGCAGAATGGAGGAGGTAAGTTGGAGACGATGCCCCTCTACTTGGAAG A G SCD Ensembl:ENSG00000099194 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:100348084..100348215 26863196 MeRIP-seq:(Medium) rs1278432416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26509,Human_RBP_ID_367708,Human_RBP_ID_805836,Human_RBP_ID_864281,Human_RBP_ID_1439964,Human_RBP_ID_4136004,Human_RBP_ID_17225068,Human_RBP_ID_18187989,Human_RBP_ID_19452028,Human_RBP_ID_22431839,Human_RBP_ID_22787056,Human_RBP_ID_26872852,Human_RBP_ID_27403106 Human_Splice_Rec_1168226 Human_miRNA_ID_1538867,Human_miRNA_ID_1593067,Human_miRNA_ID_2390289,Human_miRNA_ID_2789296,Human_miRNA_ID_2818908 RMVar_hsa_circ_85923,RMVar_hsa_circ_46856,RMVar_hsa_circ_145624 79741 RMVar_ID_79741 Human_SNP_ID_444263164 m1A Human chr10 + 100348145 100348145 100348145 GGGTCCTGCAGAATGGAGGAGATAAGTTGGAGACGATGCCCCTCTACTTGGAAGACGACATTCGC GGGTCCTGCAGAATGGAGGAGATAAGTTGGAGCCGATGCCCCTCTACTTGGAAGACGACATTCGC A C SCD Ensembl:ENSG00000099194 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100348051..100348225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_26509,Human_RBP_ID_367708,Human_RBP_ID_864281,Human_RBP_ID_1439964,Human_RBP_ID_1758322,Human_RBP_ID_4101453,Human_RBP_ID_5915794,Human_RBP_ID_9254157,Human_RBP_ID_17767415,Human_RBP_ID_18187989,Human_RBP_ID_18584763,Human_RBP_ID_19452028,Human_RBP_ID_22431840,Human_RBP_ID_22787056,Human_RBP_ID_23427933,Human_RBP_ID_26872852,Human_RBP_ID_27188495 Human_Splice_Rec_1168226 Human_miRNA_ID_1538867,Human_miRNA_ID_1593067,Human_miRNA_ID_2390289,Human_miRNA_ID_2591524,Human_miRNA_ID_2789296,Human_miRNA_ID_2818908 RMVar_hsa_circ_85923,RMVar_hsa_circ_46856,RMVar_hsa_circ_145624 79742 RMVar_ID_79742 Human_SNP_ID_444263165 m1A Human chr10 + 100348145 100348145 100348145 GGGTCCTGCAGAATGGAGGAGATAAGTTGGAGACGATGCCCCTCTACTTGGAAGACGACATTCGC GGGTCCTGCAGAATGGAGGAGATAAGTTGGAGTCGATGCCCCTCTACTTGGAAGACGACATTCGC A T SCD Ensembl:ENSG00000099194 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100348051..100348225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_26509,Human_RBP_ID_367708,Human_RBP_ID_864281,Human_RBP_ID_1439964,Human_RBP_ID_1758322,Human_RBP_ID_4101453,Human_RBP_ID_5915794,Human_RBP_ID_9254157,Human_RBP_ID_17767415,Human_RBP_ID_18187989,Human_RBP_ID_18584763,Human_RBP_ID_19452028,Human_RBP_ID_22431840,Human_RBP_ID_22787056,Human_RBP_ID_23427933,Human_RBP_ID_26872852,Human_RBP_ID_27188495 Human_Splice_Rec_1168226 Human_miRNA_ID_1538867,Human_miRNA_ID_1593067,Human_miRNA_ID_2390289,Human_miRNA_ID_2591524,Human_miRNA_ID_2789296,Human_miRNA_ID_2818908 RMVar_hsa_circ_85923,RMVar_hsa_circ_46856,RMVar_hsa_circ_145624 79743 RMVar_ID_79743 Human_SNP_ID_444265102 m1A Human chr10 - 100356724 100356724 100356724 CCAAGTGAAACCAGGATATTCTCCCGGGGGCTAATGTTCTTGTCATAAGGACGATATCCGAAGAG CCAAGTGAAACCAGGATATTCTCCCGGGGGCTGATGTTCTTGTCATAAGGACGATATCCGAAGAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:100356676..100356775 26863196 MeRIP-seq:(Medium) rs749014916 Functional Loss SNV dbSNP153 33..33 33 - - - 79744 RMVar_ID_79744 Human_SNP_ID_444266369 m1A Human chr10 - 100362151 100362151 100362151 GCTGCCTATAGATCCTGTCCCTCAGCCTCTCCATCTCATGTCCAGCAGTGGAGAGGAAATTGGCA GCTGCCTATAGATCCTGTCCCTCAGCCTCTCCGTCTCATGTCCAGCAGTGGAGAGGAAATTGGCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:100362101..100362175 26863196 MeRIP-seq:(Medium) rs1351196841 Functional Loss SNV dbSNP153 33..33 33 - - - 79745 RMVar_ID_79745 Human_SNP_ID_444266377 m1A Human chr10 - 100362198 100362198 100362198 GGCAACGTGTTCTCAGATCCCTTCCTATGTGAAGTTCGCTCTTAGAAGCTGCCTATAGATCCTGT GGCAACGTGTTCTCAGATCCCTTCCTATGTGATGTTCGCTCTTAGAAGCTGCCTATAGATCCTGT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100362076..100362250 32194978 MeRIP-seq:(Medium) rs1222711170 Functional Loss SNV dbSNP153 33..33 33 - - - 79746 RMVar_ID_79746 Human_SNP_ID_444266470 m1A Human chr10 - 100362659 100362659 100362659 GTGAAAGTGGCAGCTAGCTCTACTTTCAAAAGAGAAGCAGTGGTTCAGTGACCCTGAGCATTCTG GTGAAAGTGGCAGCTAGCTCTACTTTCAAAAGTGAAGCAGTGGTTCAGTGACCCTGAGCATTCTG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:100362609..100362796 26863196 MeRIP-seq:(Medium) rs1360855295 Functional Loss SNV dbSNP153 33..33 33 - - - 79747 RMVar_ID_79747 Human_SNP_ID_444266475 m1A Human chr10 - 100362676 100362676 100362676 GACACTGCGGAGGCCACGTGAAAGTGGCAGCTAGCTCTACTTTCAAAAGAGAAGCAGTGGTTCAG GACACTGCGGAGGCCACGTGAAAGTGGCAGCTGGCTCTACTTTCAAAAGAGAAGCAGTGGTTCAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:100362626..100362786 26863196 MeRIP-seq:(Medium) rs200685078 Functional Loss SNV dbSNP153 33..33 33 - - - 79748 RMVar_ID_79748 Human_SNP_ID_444266565 m1A Human chr10 + 100363091 100363091 100363091 CACCTCGAAAGGAGGCCCTGTTCCCTGGAGTCAGGGTGAACTGCAAAGCTTTGGCTGAGACCTGG CACCTCGAAAGGAGGCCCTGTTCCCTGGAGTCGGGGTGAACTGCAAAGCTTTGGCTGAGACCTGG A G SCD Ensembl:ENSG00000099194 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:100363043..100363162 26863196 MeRIP-seq:(Medium) rs1005714255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367808,Human_RBP_ID_980994,Human_RBP_ID_3336118,Human_RBP_ID_4101577,Human_RBP_ID_5086688,Human_RBP_ID_5092600,Human_RBP_ID_5164729,Human_RBP_ID_5915922,Human_RBP_ID_8173078,Human_RBP_ID_8323683,Human_RBP_ID_8756642,Human_RBP_ID_8981267,Human_RBP_ID_9274335,Human_RBP_ID_11230862,Human_RBP_ID_17183844,Human_RBP_ID_17225109,Human_RBP_ID_17345775,Human_RBP_ID_17457257,Human_RBP_ID_17679217,Human_RBP_ID_18236742,Human_RBP_ID_18408524,Human_RBP_ID_18544102,Human_RBP_ID_19577282,Human_RBP_ID_22378467,Human_RBP_ID_23428011,Human_RBP_ID_26398678,Human_RBP_ID_27188550 Human_miRNA_ID_75287,Human_miRNA_ID_78454,Human_miRNA_ID_119032,Human_miRNA_ID_122840,Human_miRNA_ID_1005648,Human_miRNA_ID_1860177,Human_miRNA_ID_2453984 RMVar_hsa_circ_95357,RMVar_hsa_circ_105925,RMVar_hsa_circ_145626,RMVar_hsa_circ_116351,RMVar_hsa_circ_145629,RMVar_hsa_circ_145630 79749 RMVar_ID_79749 Human_SNP_ID_444269085 m1A Human chr10 + 100373686 100373686 100373686 ATGCGGACATGCCACTCAGTCCGGCCGCGAACAGTGCTCCAGAACTCAGAGAGTTTTCCAGACGG ATGCGGACATGCCACTCAGTCCGGCCGCGAACGGTGCTCCAGAACTCAGAGAGTTTTCCAGACGG A G OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:100373635..100373805 26863196 MeRIP-seq:(Medium) rs958415613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1440020,Human_RBP_ID_11230963,Human_RBP_ID_18416162,Human_RBP_ID_23428067,Human_RBP_ID_26316567 Human_miRNA_ID_3196407 79750 RMVar_ID_79750 Human_SNP_ID_444269230 m1A Human chr10 + 100374331 100374331 100374331 CAAAAGCTGGGATAGTCACGGTGGGAATGGAAAGGAAGGGCACAAGCTGAGAGGCATTTGGGAGG CAAAAGCTGGGATAGTCACGGTGGGAATGGAAGGGAAGGGCACAAGCTGAGAGGCATTTGGGAGG A G OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100374014..100374525 26863196 MeRIP-seq:(Medium) rs894139911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1077276,Human_RBP_ID_3365882,Human_RBP_ID_8245741,Human_RBP_ID_8323717 79751 RMVar_ID_79751 Human_SNP_ID_444294540 m1A Human chr10 - 100481518 100481518 100481518 GAAAGCTCGAGCATTGAGGGGGAAAGAGGGGTACAATTGAAATATGGAACAACGATGTTGGAAAT GAAAGCTCGAGCATTGAGGGGGAAAGAGGGGTGCAATTGAAATATGGAACAACGATGTTGGAAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100481436..100481522 26863196 MeRIP-seq:(Medium) rs867295241 Functional Loss SNV dbSNP153 33..33 33 - - - 79752 RMVar_ID_79752 Human_SNP_ID_444303846 m1A Human chr10 - 100518289 100518289 100518289 AGCATTCAAAGTATAGGGAACAGCATTTGTAAAGGCTCTAAGGAAGGAAAATGTCAGGAAATTAA AGCATTCAAAGTATAGGGAACAGCATTTGTAAGGGCTCTAAGGAAGGAAAATGTCAGGAAATTAA T C AL133352.1,SEC31B Ensembl:ENSG00000255339,Ensembl:ENSG00000075826 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100518238..100518341 26863196 MeRIP-seq:(Medium) rs1181378698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11231973 RMVar_hsa_circ_78321,RMVar_hsa_circ_145636 79753 RMVar_ID_79753 Human_SNP_ID_444306025 m1A Human chr10 - 100526978 100526978 100526978 GACCAGCCGGGCCTGAGGTTGAACTGGGGTGAACCGGTAAGAGAACCATATCTCATTTGACCTTC GACCAGCCGGGCCTGAGGTTGAACTGGGGTGAGCCGGTAAGAGAACCATATCTCATTTGACCTTC T C NDUFB8,AL133352.1 Ensembl:ENSG00000166136,Ensembl:ENSG00000255339 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755572616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747725,Human_RBP_ID_805830,Human_RBP_ID_864271,Human_RBP_ID_3937995,Human_RBP_ID_9361497,Human_RBP_ID_11232226,Human_RBP_ID_18971104,Human_RBP_ID_22431578,Human_RBP_ID_22787164,Human_RBP_ID_26316569,Human_RBP_ID_27802276 Human_Splice_Rec_1168742,Human_Splice_Rec_1168743,Human_Splice_Rec_1168764,Human_Splice_Rec_1168765,Human_Splice_Rec_1168782,Human_Splice_Rec_1168783,Human_Splice_Rec_1168800,Human_Splice_Rec_1168801,Human_Splice_Rec_1168808,Human_Splice_Rec_1168809,Human_Splice_Rec_1168818,Human_Splice_Rec_1168819,Human_Splice_Rec_1168826,Human_Splice_Rec_1168827,Human_Splice_Rec_1168834,Human_Splice_Rec_1168835,Human_Splice_Rec_1168842,Human_Splice_Rec_1168843,Human_Splice_Rec_1168850,Human_Splice_Rec_1168851,Human_Splice_Rec_1168856,Human_Splice_Rec_1168860 Human_miRNA_ID_2923712,Human_miRNA_ID_2923713,Human_miRNA_ID_3002652,Human_miRNA_ID_3002653 RMVar_hsa_circ_88793,RMVar_hsa_circ_78321,RMVar_hsa_circ_145636,RMVar_hsa_circ_124700,RMVar_hsa_circ_98383,RMVar_hsa_circ_145639,RMVar_hsa_circ_145640,RMVar_hsa_circ_145643,RMVar_hsa_circ_145638,RMVar_hsa_circ_328681 79754 RMVar_ID_79754 Human_SNP_ID_444306059 m1A Human chr10 - 100527072 100527072 100527072 CCCTTTCCAGAAGTTCTTGCTGTCTTTCAGGTATGGCGACTACCCGAAGCTCCCTGACCGCTCAC CCCTTTCCAGAAGTTCTTGCTGTCTTTCAGGTGTGGCGACTACCCGAAGCTCCCTGACCGCTCAC T C NDUFB8,AL133352.1 Ensembl:ENSG00000166136,Ensembl:ENSG00000255339 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr10:100526976..100529091;chr10:100527022..100529525 26863196,32194978 MeRIP-seq:(Medium) rs753173137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225416,Human_RBP_ID_805830,Human_RBP_ID_864271,Human_RBP_ID_9360648,Human_RBP_ID_17648179,Human_RBP_ID_18971105,Human_RBP_ID_22431579,Human_RBP_ID_23206531,Human_RBP_ID_23428275,Human_RBP_ID_26316570 Human_Splice_Rec_1168742,Human_Splice_Rec_1168743,Human_Splice_Rec_1168764,Human_Splice_Rec_1168765,Human_Splice_Rec_1168782,Human_Splice_Rec_1168783,Human_Splice_Rec_1168800,Human_Splice_Rec_1168801,Human_Splice_Rec_1168808,Human_Splice_Rec_1168809,Human_Splice_Rec_1168818,Human_Splice_Rec_1168819,Human_Splice_Rec_1168826,Human_Splice_Rec_1168827,Human_Splice_Rec_1168834,Human_Splice_Rec_1168835,Human_Splice_Rec_1168842,Human_Splice_Rec_1168843,Human_Splice_Rec_1168850,Human_Splice_Rec_1168851,Human_Splice_Rec_1168856,Human_Splice_Rec_1168860 RMVar_hsa_circ_88793,RMVar_hsa_circ_78321,RMVar_hsa_circ_145636,RMVar_hsa_circ_124700,RMVar_hsa_circ_98383,RMVar_hsa_circ_145639,RMVar_hsa_circ_145640,RMVar_hsa_circ_145643,RMVar_hsa_circ_145638,RMVar_hsa_circ_328681 79755 RMVar_ID_79755 Human_SNP_ID_444306735 m1A Human chr10 - 100529817 100529817 100529817 GGCGGTGGCCAGGGCCGGGGTCTTGGGAGTCCAGTGGCTGCAAAGGGCATCCCGGAACGTGATGC GGCGGTGGCCAGGGCCGGGGTCTTGGGAGTCCGGTGGCTGCAAAGGGCATCCCGGAACGTGATGC T C NDUFB8,AL133352.1 Ensembl:ENSG00000166136,Ensembl:ENSG00000255339 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:100529328..100529902;chr10:100526976..100529875;chr10:100526976..100529881 26863196 MeRIP-seq:(Medium) rs755087128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29050,Human_RBP_ID_225419,Human_RBP_ID_367927,Human_RBP_ID_747727,Human_RBP_ID_805832,Human_RBP_ID_864274,Human_RBP_ID_4101729,Human_RBP_ID_5313086,Human_RBP_ID_5459772,Human_RBP_ID_9360652,Human_RBP_ID_18416163,Human_RBP_ID_22431866,Human_RBP_ID_23112891,Human_RBP_ID_23206533,Human_RBP_ID_23428282,Human_RBP_ID_24542125,Human_RBP_ID_24556843,Human_RBP_ID_26315967,Human_RBP_ID_26873014,Human_RBP_ID_27802277 Human_Splice_Rec_1168739,Human_Splice_Rec_1168761,Human_Splice_Rec_1168779,Human_Splice_Rec_1168797,Human_Splice_Rec_1168805,Human_Splice_Rec_1168815,Human_Splice_Rec_1168831,Human_Splice_Rec_1168839,Human_Splice_Rec_1168847,Human_Splice_Rec_1168853,Human_Splice_Rec_1168857,Human_Splice_Rec_1168861 Human_miRNA_ID_2541895,Human_miRNA_ID_2543769,Human_miRNA_ID_2545619,Human_miRNA_ID_2547474,Human_miRNA_ID_2549338,Human_miRNA_ID_2551207,Human_miRNA_ID_2556614,Human_miRNA_ID_2558496,Human_miRNA_ID_2588915 RMVar_hsa_circ_124700,RMVar_hsa_circ_145638 79756 RMVar_ID_79756 Human_SNP_ID_444306736 m1A Human chr10 - 100529817 100529817 100529817 GGCGGTGGCCAGGGCCGGGGTCTTGGGAGTCCAGTGGCTGCAAAGGGCATCCCGGAACGTGATGC GGCGGTGGCCAGGGCCGGGGTCTTGGGAGTCCCGTGGCTGCAAAGGGCATCCCGGAACGTGATGC T G NDUFB8,AL133352.1 Ensembl:ENSG00000166136,Ensembl:ENSG00000255339 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:100529328..100529902;chr10:100526976..100529875;chr10:100526976..100529881 26863196 MeRIP-seq:(Medium) rs755087128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29050,Human_RBP_ID_225419,Human_RBP_ID_367927,Human_RBP_ID_747727,Human_RBP_ID_805832,Human_RBP_ID_864274,Human_RBP_ID_4101729,Human_RBP_ID_5313086,Human_RBP_ID_5459772,Human_RBP_ID_9360652,Human_RBP_ID_18416163,Human_RBP_ID_22431866,Human_RBP_ID_23112891,Human_RBP_ID_23206533,Human_RBP_ID_23428282,Human_RBP_ID_24542125,Human_RBP_ID_24556843,Human_RBP_ID_26315967,Human_RBP_ID_26873014,Human_RBP_ID_27802277 Human_Splice_Rec_1168739,Human_Splice_Rec_1168761,Human_Splice_Rec_1168779,Human_Splice_Rec_1168797,Human_Splice_Rec_1168805,Human_Splice_Rec_1168815,Human_Splice_Rec_1168831,Human_Splice_Rec_1168839,Human_Splice_Rec_1168847,Human_Splice_Rec_1168853,Human_Splice_Rec_1168857,Human_Splice_Rec_1168861 Human_miRNA_ID_2541895,Human_miRNA_ID_2543769,Human_miRNA_ID_2545619,Human_miRNA_ID_2547474,Human_miRNA_ID_2549338,Human_miRNA_ID_2551207,Human_miRNA_ID_2556614,Human_miRNA_ID_2558496,Human_miRNA_ID_2588915 RMVar_hsa_circ_124700,RMVar_hsa_circ_145638 79757 RMVar_ID_79757 Human_SNP_ID_444312620 m1A Human chr10 - 100553127 100553125 100553127 ACCAGCTTCCCGGGCCTGACATCATTCTCACAAAGTCTCCTCAGCAATCCCTGCACCTCTCCCCT ACCAGCTTCCCGGGCCTGACATCATTCTCACA__GTCTCCTCAGCAATCCCTGCACCTCTCCCCT CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:100552986..100553172;chr10:100553020..100553150 26863196 MeRIP-seq:(Medium) rs144237406 Functional Loss DEL dbSNP153 33..34 33 - - - 79758 RMVar_ID_79758 Human_SNP_ID_444314975 m1A Human chr10 - 100562989 100562989 100562989 CAATCCATCACCCTCAACACGCCCGTCCACCCACACCCCCACCTCCCCGCTCCTGAGCGGCACCC CAATCCATCACCCTCAACACGCCCGTCCACCCCCACCCCCACCTCCCCGCTCCTGAGCGGCACCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100562940..100563034 26863196 MeRIP-seq:(Medium) rs1213500938 Functional Loss SNV dbSNP153 33..33 33 - - - 79759 RMVar_ID_79759 Human_SNP_ID_444420524 m1A Human chr10 - 100986551 100986551 100986551 TTTCTTTCCAGTGCCTGCTTCTGGGGGCAGTGACCTTGTGAACCACTCATTTTTATGCAAGTGGC TTTCTTTCCAGTGCCTGCTTCTGGGGGCAGTGTCCTTGTGAACCACTCATTTTTATGCAAGTGGC T A MRPL43 Ensembl:ENSG00000055950 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:100986446..100986646 32194978 MeRIP-seq:(Medium) rs1039069596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368088,Human_RBP_ID_1758619,Human_RBP_ID_17648182,Human_RBP_ID_23429033,Human_RBP_ID_26873089 Human_Splice_Rec_1169214,Human_Splice_Rec_1169228 Human_miRNA_ID_2514659,Human_miRNA_ID_2779697,Human_miRNA_ID_2942215 RMVar_hsa_circ_112680,RMVar_hsa_circ_145687,RMVar_hsa_circ_102356,RMVar_hsa_circ_145686 79760 RMVar_ID_79760 Human_SNP_ID_444420620 m1A Human chr10 - 100986810 100986810 100986810 TAGCATCCAGGGCCAGTGGCACCCCTTCACCAACAAGCCGACCACGTTCCGCGGGCTACGCCCCC TAGCATCCAGGGCCAGTGGCACCCCTTCACCAGCAAGCCGACCACGTTCCGCGGGCTACGCCCCC T C MRPL43 Ensembl:ENSG00000055950 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:100986760..100986923 26863196 MeRIP-seq:(Medium) rs1481902885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368100,Human_RBP_ID_1440208,Human_RBP_ID_5458713,Human_RBP_ID_22431867,Human_RBP_ID_22489170 Human_Splice_Rec_1169145,Human_Splice_Rec_1169153,Human_Splice_Rec_1169161,Human_Splice_Rec_1169169,Human_Splice_Rec_1169185,Human_Splice_Rec_1169195,Human_Splice_Rec_1169203,Human_Splice_Rec_1169227 RMVar_hsa_circ_7515,RMVar_hsa_circ_112680,RMVar_hsa_circ_145687,RMVar_hsa_circ_102356,RMVar_hsa_circ_145686 79761 RMVar_ID_79761 Human_SNP_ID_444420896 m1A Human chr10 + 100987416 100987416 100987416 ACCCAGTCCGTTGTGGAGAACGCTGGCCAAGAAGCGGCTCGGAGTCCCGCGCGCCGTCATAGCTA ACCCAGTCCGTTGTGGAGAACGCTGGCCAAGAGGCGGCTCGGAGTCCCGCGCGCCGTCATAGCTA A G TWNK Ensembl:ENSG00000107815 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100987365..100987475 26863196 MeRIP-seq:(Medium) rs1294828350 Functional Loss SNV dbSNP153 33..33 33 - - - 79762 RMVar_ID_79762 Human_SNP_ID_444421011 m1A Human chr10 + 100987608 100987608 100987608 AGACTCACGTTGCCGGCGAAGTGGGAGAGAGAAAAGTGGTAACCTGGGGCTGGGGGCCGGCGCGG AGACTCACGTTGCCGGCGAAGTGGGAGAGAGAGAAGTGGTAACCTGGGGCTGGGGGCCGGCGCGG A G TWNK Ensembl:ENSG00000107815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:100987551..100988191;chr10:100987551..100988213;chr10:100987551..100988188 26863196 MeRIP-seq:(Medium) rs908486981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4102106,Human_RBP_ID_5487371 Human_Splice_Rec_1169421,Human_Splice_Rec_1169435 RMVar_hsa_circ_145688 79763 RMVar_ID_79763 Human_SNP_ID_444421012 m1A Human chr10 + 100987608 100987608 100987608 AGACTCACGTTGCCGGCGAAGTGGGAGAGAGAAAAGTGGTAACCTGGGGCTGGGGGCCGGCGCGG AGACTCACGTTGCCGGCGAAGTGGGAGAGAGATAAGTGGTAACCTGGGGCTGGGGGCCGGCGCGG A T TWNK Ensembl:ENSG00000107815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:100987551..100988191;chr10:100987551..100988213;chr10:100987551..100988188 26863196 MeRIP-seq:(Medium) rs908486981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4102106,Human_RBP_ID_5487371 Human_Splice_Rec_1169421,Human_Splice_Rec_1169435 RMVar_hsa_circ_145688 79764 RMVar_ID_79764 Human_SNP_ID_444421397 m1A Human chr10 - 100988882 100988882 100988882 TCCTCGTAGCTCACTCCATCCCCCTGGCATTTAGCCTCTAGGAGCTTCAGGCCTCGTAATCCTGA TCCTCGTAGCTCACTCCATCCCCCTGGCATTTGGCCTCTAGGAGCTTCAGGCCTCGTAATCCTGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:100988729..100989076 32194978 MeRIP-seq:(Medium) rs368863664 Functional Loss SNV dbSNP153 33..33 33 - - - 79765 RMVar_ID_79765 Human_SNP_ID_444424437 m1A Human chr10 + 100999880 100999844 100999880 AGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT _________________________________GCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT GGCCAGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGA G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr10:100999824..100999982;chr10:100999781..100999925 26863196,26863410 MeRIP-seq:(Medium) rs1466459576 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_3364085,Human_RBP_ID_4136014,Human_RBP_ID_5234636,Human_RBP_ID_8172301,Human_RBP_ID_22708595,Human_RBP_ID_23255661 Human_Splice_Rec_1169483 RMVar_hsa_circ_121630,RMVar_hsa_circ_145692 79766 RMVar_ID_79766 Human_SNP_ID_444424452 m1A Human chr10 + 100999880 100999856 100999880 AGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT AGGGCCGGG________________________GCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT GGCCGGGGCCGGGGCCGGAGCCGGA G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr10:100999824..100999982;chr10:100999781..100999925 26863196,26863410 MeRIP-seq:(Medium) rs1327641164 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_3364085,Human_RBP_ID_4136014,Human_RBP_ID_5234636,Human_RBP_ID_8172301,Human_RBP_ID_22708595,Human_RBP_ID_23255661 Human_Splice_Rec_1169483 RMVar_hsa_circ_121630,RMVar_hsa_circ_145692 79767 RMVar_ID_79767 Human_SNP_ID_444424457 m1A Human chr10 + 100999880 100999862 100999880 AGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT AGGGCCGGGGCCGGG__________________GCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT GGCCGGGGCCGGAGCCGGA G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr10:100999824..100999982;chr10:100999781..100999925 26863196,26863410 MeRIP-seq:(Medium) rs922290267 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_3364085,Human_RBP_ID_4136014,Human_RBP_ID_5234636,Human_RBP_ID_8172301,Human_RBP_ID_22708595,Human_RBP_ID_23255661 Human_Splice_Rec_1169483 RMVar_hsa_circ_121630,RMVar_hsa_circ_145692 79768 RMVar_ID_79768 Human_SNP_ID_444424470 m1A Human chr10 + 100999880 100999880 100999880 AGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT AGGGCCGGGGCCGGGGCCGGGGCCGGAGCCGGGGCCGGGGCCGGGCGGCGCGCCTGTGGAGCGCT A G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr10:100999824..100999982;chr10:100999781..100999925 26863196,26863410 MeRIP-seq:(Medium) rs1348131716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364085,Human_RBP_ID_4136014,Human_RBP_ID_5234636,Human_RBP_ID_8172301,Human_RBP_ID_22708595,Human_RBP_ID_23255661 Human_Splice_Rec_1169483 RMVar_hsa_circ_121630,RMVar_hsa_circ_145692 79769 RMVar_ID_79769 Human_SNP_ID_444425204 m1A Human chr10 - 101002667 101002667 101002667 GTGGGCCCAGGAGGGCCGTGGTGGCGGGGAGGAGCTGGCCCCCCGGGACAGGGCCGGCCTGAGAT GTGGGCCCAGGAGGGCCGTGGTGGCGGGGAGGGGCTGGCCCCCCGGGACAGGGCCGGCCTGAGAT T C lnc-PDZD7-1 RNACentral:URS00008BF54D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:101002462..101002947 26863196 MeRIP-seq:(Medium) rs1218248999 Functional Loss SNV dbSNP153 33..33 33 - - - 79770 RMVar_ID_79770 Human_SNP_ID_444425291 m1A Human chr10 + 101002848 101002848 101002848 AGGACTTCCGGACAGAGTCACCCCCCAGCCCAAGCAGTGATGTTGAGGATGCCCGAGAGCAGCGG AGGACTTCCGGACAGAGTCACCCCCCAGCCCAGGCAGTGATGTTGAGGATGCCCGAGAGCAGCGG A G LZTS2 Ensembl:ENSG00000107816 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:101002826..101002850 26863196 MeRIP-seq:(Medium) rs1295328753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747226,Human_RBP_ID_5917254,Human_RBP_ID_11234411,Human_RBP_ID_18971128,Human_RBP_ID_22029489,Human_RBP_ID_23112946 Human_Splice_Rec_1169459,Human_Splice_Rec_1169463,Human_Splice_Rec_1169473,Human_Splice_Rec_1169477,Human_Splice_Rec_1169485 RMVar_hsa_circ_121630,RMVar_hsa_circ_145692 79771 RMVar_ID_79771 Human_SNP_ID_444426834 m1A Human chr10 - 101007639 101007637 101007639 GGTCTGACTTCAGCCCCCTCACTCCAGGAGAGAGGCTGCAGAGCTCAAACCTGGGAACCGAGCCC GGTCTGACTTCAGCCCCCTCACTCCAGGAGAG__GCTGCAGAGCTCAAACCTGGGAACCGAGCCC CCT C lnc-PDZD7-1 RNACentral:URS00008BF54D lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101007485..101007775 32194978 MeRIP-seq:(Medium) rs1471220591 Functional Loss DEL dbSNP153 33..34 33 - - - 79772 RMVar_ID_79772 Human_SNP_ID_444434362 m1A Human chr10 - 101031338 101031338 101031338 GAACAAGCCAGACCCAAGCCCTAAATTTGCGGAATGAGCTAGGGCGTCAGAACCAGAACTGGGGT GAACAAGCCAGACCCAAGCCCTAAATTTGCGGTATGAGCTAGGGCGTCAGAACCAGAACTGGGGT T A PDZD7 Ensembl:ENSG00000186862 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:101031291..101031430;chr10:101031291..101031444;chr10:101031290..101031436 26863196 MeRIP-seq:(Medium) rs777665375 Functional Loss SNV dbSNP153 33..33 33 - - - 79773 RMVar_ID_79773 Human_SNP_ID_444434702 m1A Human chr10 - 101032464 101032464 101032464 GAGCGAGCACTTACGCTTTCCATCGCTCTCTGAAGCTCTCAGAACCGCCTTCCTCTCTGCCTCCG GAGCGAGCACTTACGCTTTCCATCGCTCTCTGCAGCTCTCAGAACCGCCTTCCTCTCTGCCTCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:101032422..101032522 26863196 MeRIP-seq:(Medium) rs774212921 Functional Loss SNV dbSNP153 33..33 33 - - - 79774 RMVar_ID_79774 Human_SNP_ID_444436895 m1A Human chr10 + 101040603 101040601 101040603 TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTAATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTTGTGTTCCATTGACTTTTTTTTTTTTTTT__ATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTA T SFXN3 Ensembl:ENSG00000107819 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1554839530 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11234440,Human_RBP_ID_24400980,Human_RBP_ID_24455933 Human_miRNA_ID_264208,Human_miRNA_ID_2047576 RMVar_hsa_circ_125598,RMVar_hsa_circ_145696,RMVar_hsa_circ_116236,RMVar_hsa_circ_145700 79775 RMVar_ID_79775 Human_SNP_ID_444436897 m1A Human chr10 + 101040603 101040602 101040603 TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTAATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTTGTGTTCCATTGACTTTTTTTTTTTTTTTT_ATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TA T SFXN3 Ensembl:ENSG00000107819 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35045966 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11234440,Human_RBP_ID_24400980,Human_RBP_ID_24455933 Human_miRNA_ID_264208,Human_miRNA_ID_2047576 RMVar_hsa_circ_125598,RMVar_hsa_circ_145696,RMVar_hsa_circ_116236,RMVar_hsa_circ_145700 79776 RMVar_ID_79776 Human_SNP_ID_444436899 m1A Human chr10 + 101040603 101040603 101040603 TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTAATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTGATGGAGTTTCACTATTTTGCCCAGGCTGGAGT A G SFXN3 Ensembl:ENSG00000107819 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs807048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11234440,Human_RBP_ID_24400980,Human_RBP_ID_24455933 Human_miRNA_ID_264208,Human_miRNA_ID_2047576 RMVar_hsa_circ_125598,RMVar_hsa_circ_145696,RMVar_hsa_circ_116236,RMVar_hsa_circ_145700 79777 RMVar_ID_79777 Human_SNP_ID_444436900 m1A Human chr10 + 101040603 101040603 101040603 TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTAATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTTATGGAGTTTCACTATTTTGCCCAGGCTGGAGT A T SFXN3 Ensembl:ENSG00000107819 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs807048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11234440,Human_RBP_ID_24400980,Human_RBP_ID_24455933 Human_miRNA_ID_264208,Human_miRNA_ID_2047576 RMVar_hsa_circ_125598,RMVar_hsa_circ_145696,RMVar_hsa_circ_116236,RMVar_hsa_circ_145700 79778 RMVar_ID_79778 Human_SNP_ID_444441950 m1A Human chr10 - 101062041 101062041 101062041 GTCCGAAAGAAAAGGTTATGGAAAGAAAGCAGAGGCGCAGTCAGCCGGGCCCGCCGGCCACCTCT GTCCGAAAGAAAAGGTTATGGAAAGAAAGCAGGGGCGCAGTCAGCCGGGCCCGCCGGCCACCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:101061990..101062099 26863196 MeRIP-seq:(Medium) rs1410643043 Functional Loss SNV dbSNP153 33..33 33 - - - 79779 RMVar_ID_79779 Human_SNP_ID_444442935 m1A Human chr10 - 101064932 101064932 101064932 ACACTATAGCCGCTCACCCACCCCCATGGGCCAGAGCTCTGGACCTAGTAGTAATCGTCATTCTC ACACTATAGCCGCTCACCCACCCCCATGGGCCGGAGCTCTGGACCTAGTAGTAATCGTCATTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:101064883..101065241 26863196 MeRIP-seq:(Medium) rs755106497 Functional Loss SNV dbSNP153 33..33 33 - - - 79780 RMVar_ID_79780 Human_SNP_ID_444516213 m1A Human chr10 + 101354220 101354220 101354220 CGGCCGAGGCGGTGCTGCAAGAGAAGGCACTCAAGTTTATGGTGAGGAGACGGTGGAGGCCGGGG CGGCCGAGGCGGTGCTGCAAGAGAAGGCACTCGAGTTTATGGTGAGGAGACGGTGGAGGCCGGGG A G BTRC Ensembl:ENSG00000166167 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:101354171..101354401 26863196 MeRIP-seq:(Medium) rs1355896539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416170,Human_RBP_ID_19045739 Human_Splice_Rec_1169811,Human_Splice_Rec_1169837,Human_Splice_Rec_1169845,Human_Splice_Rec_1169871,Human_Splice_Rec_1169899 79781 RMVar_ID_79781 Human_SNP_ID_444542995 m1A Human chr10 + 101461949 101461949 101461949 TTTACTCCCAAAGGATAAGATTGAAGATAATGAGAACTGAATTAAAGCTTACTTTCTTTCACAGA TTTACTCCCAAAGGATAAGATTGAAGATAATGTGAACTGAATTAAAGCTTACTTTCTTTCACAGA A T BTRC Ensembl:ENSG00000166167 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:101461946..101462019 26863196 MeRIP-seq:(Medium) rs1313907607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5634,RMVar_hsa_circ_282112,RMVar_hsa_circ_306626,RMVar_hsa_circ_96023,RMVar_hsa_circ_145702,RMVar_hsa_circ_145704,RMVar_hsa_circ_145705,RMVar_hsa_circ_145703,RMVar_hsa_circ_145706,RMVar_hsa_circ_273415 79782 RMVar_ID_79782 Human_SNP_ID_444570861 m1A Human chr10 - 101578206 101578206 101578206 GTGGGCACAGAGTCAGAAGGAGACTGTATTGGAGGAGGAGCCTGGAGAGGCCCCATGCTGGGAGT GTGGGCACAGAGTCAGAAGGAGACTGTATTGGTGGAGGAGCCTGGAGAGGCCCCATGCTGGGAGT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:101578169..101578422 26863196 MeRIP-seq:(Medium) rs3730483 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_17767904 79783 RMVar_ID_79783 Human_SNP_ID_444570873 m1A Human chr10 - 101578252 101578252 101578252 AGTGGGGTCATGGAAGGAGCTTCAGGCAGCCCAAGTATGAGGAGGAGTGGGCACAGAGTCAGAAG AGTGGGGTCATGGAAGGAGCTTCAGGCAGCCCGAGTATGAGGAGGAGTGGGCACAGAGTCAGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:101578205..101578294 26863196 MeRIP-seq:(Medium) rs1257332492 Functional Loss SNV dbSNP153 33..33 33 - - - 79784 RMVar_ID_79784 Human_SNP_ID_444571110 m1A Human chr10 - 101579322 101579322 101579322 CCAACCACCAGCTTCCTCAGCGAGCAGGGCCCAGGGCTCTGGGCCTGAAGCAAGAGCCAGCCCGG CCAACCACCAGCTTCCTCAGCGAGCAGGGCCCGGGGCTCTGGGCCTGAAGCAAGAGCCAGCCCGG T C POLL Ensembl:ENSG00000166169 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101578931..101579578 32194978 MeRIP-seq:(Medium) rs1333464827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225921,Human_RBP_ID_368233 79785 RMVar_ID_79785 Human_SNP_ID_444571483 m1A Human chr10 + 101580382 101580382 101580382 CCCGTCGGTATGAACCACATGCCACACACAGCAGCCCAGAGTTAAAGGCCTGGGCTGCTTTCTGG CCCGTCGGTATGAACCACATGCCACACACAGCGGCCCAGAGTTAAAGGCCTGGGCTGCTTTCTGG A G DPCD Ensembl:ENSG00000166171 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101580334..101580434 32194978 MeRIP-seq:(Medium) rs1444377424 Functional Loss SNV dbSNP153 33..33 33 - - - 79786 RMVar_ID_79786 Human_SNP_ID_444573356 m1A Human chr10 - 101587453 101587453 101587453 CCCAAAGCCTGGTCAGGAAAGACCCTACCTCCATAGGCAAAGGGGTTGGAGGGCCTCAATTCTGG CCCAAAGCCTGGTCAGGAAAGACCCTACCTCCGTAGGCAAAGGGGTTGGAGGGCCTCAATTCTGG T C POLL Ensembl:ENSG00000166169 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101587424..101587524 32194978 MeRIP-seq:(Medium) rs1040373181 Functional Loss SNV dbSNP153 33..33 33 - - - 79787 RMVar_ID_79787 Human_SNP_ID_444573739 m1A Human chr10 - 101588402 101588402 101588402 AAAACGAAGGAGCCCGTGGGGACCCTCGAGTTACCGTCCTGCAGCAGCGCAGTCTTCTGGGCTGT AAAACGAAGGAGCCCGTGGGGACCCTCGAGTTTCCGTCCTGCAGCAGCGCAGTCTTCTGGGCTGT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:101588326..101588450 26863410 MeRIP-seq:(Medium) rs1184643720 Functional Loss SNV dbSNP153 33..33 33 - - - 79788 RMVar_ID_79788 Human_SNP_ID_444575190 m1A Human chr10 + 101594610 101594610 101594610 TTCCCAGGTAGGCCCCTTGATCTGCAAGGGACAGGGCAAGGGGAGACTTTGAGGTAAGGCATTCT TTCCCAGGTAGGCCCCTTGATCTGCAAGGGACGGGGCAAGGGGAGACTTTGAGGTAAGGCATTCT A G DPCD Ensembl:ENSG00000166171 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:101594599..101594725 26863410 MeRIP-seq:(Medium) rs575896812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91113,RMVar_hsa_circ_100583,RMVar_hsa_circ_145720,RMVar_hsa_circ_145721 79789 RMVar_ID_79789 Human_SNP_ID_444578432 m1A Human chr10 + 101609424 101609424 101609424 TGGCCGAGTCTGAGCTACAGAAGGAACTAAAGAAGGTGAAGACAGCCCACAGCAACGATGGGGAC TGGCCGAGTCTGAGCTACAGAAGGAACTAAAGGAGGTGAAGACAGCCCACAGCAACGATGGGGAC A G DPCD Ensembl:ENSG00000166171 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:101609373..101609570 32194978 MeRIP-seq:(Medium) rs775699932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862752,Human_RBP_ID_1440315,Human_RBP_ID_9360684 Human_Splice_Rec_1169952,Human_Splice_Rec_1169964,Human_Splice_Rec_1169970,Human_Splice_Rec_1169976 RMVar_hsa_circ_100583,RMVar_hsa_circ_93183,RMVar_hsa_circ_145720,RMVar_hsa_circ_83748,RMVar_hsa_circ_145723,RMVar_hsa_circ_104507,RMVar_hsa_circ_112303,RMVar_hsa_circ_145724,RMVar_hsa_circ_145726,RMVar_hsa_circ_145727 79790 RMVar_ID_79790 Human_SNP_ID_444579299 m1A Human chr10 + 101612709 101612695 101612710 CCCACCCCTCCCCCAGCATCCCAGCCCTCAGCAGCCCCTCCATCACACCTGCGTGCCGGCTGCCA CCCACCCCTCCCCCAGCAT_______________CCCCTCCATCACACCTGCGTGCCGGCTGCCA TCCCAGCCCTCAGCAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:101612707..101612791 26863196 MeRIP-seq:(Medium) rs1321092390 Functional Loss DEL dbSNP153 20..34 33 - - - 79791 RMVar_ID_79791 Human_SNP_ID_444592275 m1A Human chr10 + 101673044 101673044 101673044 GTGCTGTGAATCTTATGAATGCCAATCTTCCCATCCCTAGGAGAGAAATAAGGAGCCGACCCCCA GTGCTGTGAATCTTATGAATGCCAATCTTCCCGTCCCTAGGAGAGAAATAAGGAGCCGACCCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101667891..101676482 32194978 MeRIP-seq:(Medium) rs61742882 Functional Loss SNV dbSNP153 33..33 33 - - - 79792 RMVar_ID_79792 Human_SNP_ID_444596940 m1A Human chr10 - 101695056 101695056 101695056 CTCGGGGCCCCCCGGGAACGGCGGGCCCGGCGAGGGCGAGGGCGGAGAGGCGAGGAAGCTGCAGG CTCGGGGCCCCCCGGGAACGGCGGGCCCGGCGGGGGCGAGGGCGGAGAGGCGAGGAAGCTGCAGG T C FBXW4 Ensembl:ENSG00000107829 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:101695045..101695134 26863410 MeRIP-seq:(Medium) rs1378066946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137029 79793 RMVar_ID_79793 Human_SNP_ID_444618042 m1A Human chr10 - 101782497 101782497 101782497 TCAGGAGATCGCAGTCCCTGTGGCCAACCTCAAGCTGTCCTGCCAACCCATGGTGAGTTCCCCAG TCAGGAGATCGCAGTCCCTGTGGCCAACCTCAGGCTGTCCTGCCAACCCATGGTGAGTTCCCCAG T C NPM3 Ensembl:ENSG00000107833 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:101782484..101782582 26863410 MeRIP-seq:(Medium) rs1180058091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1170259,Human_Splice_Rec_1170267,Human_Splice_Rec_1170277,Human_Splice_Rec_1170281 Human_miRNA_ID_1998223,Human_miRNA_ID_2626690,Human_miRNA_ID_2747517 RMVar_hsa_circ_858,RMVar_hsa_circ_115577,RMVar_hsa_circ_145749,RMVar_hsa_circ_84356,RMVar_hsa_circ_145750,RMVar_hsa_circ_125657,RMVar_hsa_circ_145751 79794 RMVar_ID_79794 Human_SNP_ID_444627941 m1A Human chr10 + 101818271 101818271 101818271 CCTCGGCTTTAAGCTGGGGCGCCAGAAGCCTAAGCGGAGAGCGAGGCTGTGACCTCTCGTTCCCT CCTCGGCTTTAAGCTGGGGCGCCAGAAGCCTACGCGGAGAGCGAGGCTGTGACCTCTCGTTCCCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:101818221..101818334 32194978 MeRIP-seq:(Medium) rs1351553044 Functional Loss SNV dbSNP153 33..33 33 - - - 79795 RMVar_ID_79795 Human_SNP_ID_444627972 m1A Human chr10 + 101818360 101818352 101818361 TCCTCGTTCTCTGCCTCTGCTGCCCTCCCGATAATCTTAGGTCTTCCGCTGTTTCCCCTCCAAGC TCCTCGTTCTCTGCCTCTGCTGCCC_________TCTTAGGTCTTCCGCTGTTTCCCCTCCAAGC CTCCCGATAA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:101818301..101818425 26863410 MeRIP-seq:(Medium) rs1398604009 Functional Loss DEL dbSNP153 26..34 33 - - - 79796 RMVar_ID_79796 Human_SNP_ID_444627975 m1A Human chr10 - 101818362 101818362 101818362 GGGCTTGGAGGGGAAACAGCGGAAGACCTAAGATTATCGGGAGGGCAGCAGAGGCAGAGAACGAG GGGCTTGGAGGGGAAACAGCGGAAGACCTAAGGTTATCGGGAGGGCAGCAGAGGCAGAGAACGAG T C OGA Ensembl:ENSG00000198408 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:101818114..101818450 26863196 MeRIP-seq:(Medium) rs961640408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28330,Human_RBP_ID_746873,Human_RBP_ID_805355,Human_RBP_ID_3938005,Human_RBP_ID_5918900,Human_RBP_ID_9413168,Human_RBP_ID_11238726,Human_RBP_ID_17768027,Human_RBP_ID_18416174,Human_RBP_ID_18431156,Human_RBP_ID_22876569,Human_RBP_ID_23112892,Human_RBP_ID_24774840,Human_RBP_ID_26316598,Human_RBP_ID_26774913 RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_95277,RMVar_hsa_circ_145796 79797 RMVar_ID_79797 Human_SNP_ID_444627979 m1A Human chr10 - 101818372 101818372 101818372 GGAGAGCTCGGGGCTTGGAGGGGAAACAGCGGAAGACCTAAGATTATCGGGAGGGCAGCAGAGGC GGAGAGCTCGGGGCTTGGAGGGGAAACAGCGGCAGACCTAAGATTATCGGGAGGGCAGCAGAGGC T G OGA Ensembl:ENSG00000198408 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:101810251..101818465 26863196 MeRIP-seq:(Medium) rs1198660826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28330,Human_RBP_ID_746873,Human_RBP_ID_805355,Human_RBP_ID_4138109,Human_RBP_ID_9413168,Human_RBP_ID_11238726,Human_RBP_ID_17668488,Human_RBP_ID_18416174,Human_RBP_ID_22876569,Human_RBP_ID_23112892,Human_RBP_ID_23429816,Human_RBP_ID_24774840,Human_RBP_ID_26316599,Human_RBP_ID_26774913 RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_95277,RMVar_hsa_circ_145796 79798 RMVar_ID_79798 Human_SNP_ID_444631940 m1A Human chr10 + 101833958 101833958 101833958 CACTCCTTCCCTATCTCCAGACCCCTCCTGGTATCGCCCAGAATCCCCTCACCTCCTCATCTCCA CACTCCTTCCCTATCTCCAGACCCCTCCTGGTGTCGCCCAGAATCCCCTCACCTCCTCATCTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:101833856..101834152;chr10:101833667..101834108 26863196 MeRIP-seq:(Medium) rs900187153 Functional Loss SNV dbSNP153 33..33 33 - - - 79799 RMVar_ID_79799 Human_SNP_ID_444686083 m1A Human chr10 - 102056105 102056105 102056105 GAGCGAGCGGGCCCGGGAACGGCGCGGGTGGTAGAGGAGGAGCCGCGGGCTCGGTAAGCGGCGGC GAGCGAGCGGGCCCGGGAACGGCGCGGGTGGTTGAGGAGGAGCCGCGGGCTCGGTAAGCGGCGGC T A ARMH3 Ensembl:ENSG00000120029 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102040071..102056223 26863196 MeRIP-seq:(Medium) rs930842837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8725049,Human_RBP_ID_9413405,Human_RBP_ID_18416175,Human_RBP_ID_18971172 Human_Splice_Rec_1170621,Human_Splice_Rec_1170681 79800 RMVar_ID_79800 Human_SNP_ID_444686095 m1A Human chr10 + 102056150 102056150 102056150 GTTCCCGGGCCCGCTCGCTCTCGACGCCACCGACGCTGCCGCTGCTCCGGGCTCACGGGCGCGCT GTTCCCGGGCCCGCTCGCTCTCGACGCCACCGGCGCTGCCGCTGCTCCGGGCTCACGGGCGCGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102055949..102056238 26863196 MeRIP-seq:(Medium) rs181625032 Functional Loss SNV dbSNP153 33..33 33 - - - 79801 RMVar_ID_79801 Human_SNP_ID_444688550 m1A Human chr10 + 102065466 102065457 102065467 GACCTGGGCAAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCATGAAGCGCTCGGGGACTCTGCGG GACCTGGGCAAAGCCTGGGCGCGC__________CGGCGCCATGAAGCGCTCGGGGACTCTGCGG CTCCCGCGCAG C HPS6 Ensembl:ENSG00000166189 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102065417..102065511 26863196 MeRIP-seq:(Medium) rs1318139921 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_4136023 79802 RMVar_ID_79802 Human_SNP_ID_444688562 m1A Human chr10 + 102065475 102065475 102065475 AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCATGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCCTGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG A C HPS6 Ensembl:ENSG00000166189 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102065424..102065587 26863196 MeRIP-seq:(Medium) rs763073715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4103141 79803 RMVar_ID_79803 Human_SNP_ID_444688563 m1A Human chr10 + 102065475 102065475 102065475 AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCATGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCGTGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG A G HPS6 Ensembl:ENSG00000166189 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102065424..102065587 26863196 MeRIP-seq:(Medium) rs763073715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4103141 79804 RMVar_ID_79804 Human_SNP_ID_444688564 m1A Human chr10 + 102065475 102065475 102065475 AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCATGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG AAAGCCTGGGCGCGCTCCCGCGCAGCGGCGCCTTGAAGCGCTCGGGGACTCTGCGGCTGCTCTCG A T HPS6 Ensembl:ENSG00000166189 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102065424..102065587 26863196 MeRIP-seq:(Medium) rs763073715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4103141 79805 RMVar_ID_79805 Human_SNP_ID_444700577 m1A Human chr10 - 102109907 102109907 102109907 CAGCATCCTTGCCATGCATGTGAGTCGTGGGCAGGACCCAGGATGCAAGAGTGAAGGCAGGCGGG CAGCATCCTTGCCATGCATGTGAGTCGTGGGCGGGACCCAGGATGCAAGAGTGAAGGCAGGCGGG T C LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102109901..102109975 26863196 MeRIP-seq:(Medium) rs772506961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19045752 RMVar_hsa_circ_145868,RMVar_hsa_circ_82457,RMVar_hsa_circ_145866,RMVar_hsa_circ_125572,RMVar_hsa_circ_278496,RMVar_hsa_circ_374701,RMVar_hsa_circ_145869,RMVar_hsa_circ_95175,RMVar_hsa_circ_35668,RMVar_hsa_circ_145867,RMVar_hsa_circ_306437,RMVar_hsa_circ_145870,RMVar_hsa_circ_378908,RMVar_hsa_circ_145873,RMVar_hsa_circ_87569,RMVar_hsa_circ_145875,RMVar_hsa_circ_78046,RMVar_hsa_circ_145874 79806 RMVar_ID_79806 Human_SNP_ID_444701102 m1A Human chr10 - 102111526 102111526 102111526 GACTCCTTTCTTTCTCGTCTAGGTTGTTCCTCAAAGTCATTCAAGCTGTACTCGCCGAAGGAGCC GACTCCTTTCTTTCTCGTCTAGGTTGTTCCTCCAAGTCATTCAAGCTGTACTCGCCGAAGGAGCC T G LDB1 Ensembl:ENSG00000198728 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:102111476..102111550 32194978 MeRIP-seq:(Medium) rs1267535254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1440481,Human_RBP_ID_26873455 Human_Splice_Rec_1170690,Human_Splice_Rec_1170691,Human_Splice_Rec_1170710,Human_Splice_Rec_1170711,Human_Splice_Rec_1170730,Human_Splice_Rec_1170731 RMVar_hsa_circ_278496,RMVar_hsa_circ_145869,RMVar_hsa_circ_306437,RMVar_hsa_circ_145870,RMVar_hsa_circ_378908,RMVar_hsa_circ_353826,RMVar_hsa_circ_145880,RMVar_hsa_circ_79566 79807 RMVar_ID_79807 Human_SNP_ID_444702014 m1A Human chr10 + 102114834 102114834 102114834 CCTCCGAGCAGCCCGCCCGCCCTCCCCAGGCCACCGGGCCCCTCTGCTGGGGGCACCAGGAGAGG CCTCCGAGCAGCCCGCCCGCCCTCCCCAGGCCCCCGGGCCCCTCTGCTGGGGGCACCAGGAGAGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102114801..102114945 26863196 MeRIP-seq:(Medium) rs1378275444 Functional Loss SNV dbSNP153 33..33 33 - - - 79808 RMVar_ID_79808 Human_SNP_ID_444702015 m1A Human chr10 + 102114834 102114834 102114834 CCTCCGAGCAGCCCGCCCGCCCTCCCCAGGCCACCGGGCCCCTCTGCTGGGGGCACCAGGAGAGG CCTCCGAGCAGCCCGCCCGCCCTCCCCAGGCCGCCGGGCCCCTCTGCTGGGGGCACCAGGAGAGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102114801..102114945 26863196 MeRIP-seq:(Medium) rs1378275444 Functional Loss SNV dbSNP153 33..33 33 - - - 79809 RMVar_ID_79809 Human_SNP_ID_444702025 m1A Human chr10 + 102114864 102114864 102114864 CCACCGGGCCCCTCTGCTGGGGGCACCAGGAGAGGCAGGACCCGGCACTCACACTCACTCACACT CCACCGGGCCCCTCTGCTGGGGGCACCAGGAGGGGCAGGACCCGGCACTCACACTCACTCACACT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:102114588..102114950 26863196 MeRIP-seq:(Medium) rs868507504 Functional Loss SNV dbSNP153 33..33 33 - - - 79810 RMVar_ID_79810 Human_SNP_ID_444702045 m1A Human chr10 - 102114904 102114900 102114904 CAGGCAGCCGGCGGGCGCTGCGTGTGTGTTTGAGTGTGCGAGTGTGAGTGAGTGTGAGTGCCGGG CAGGCAGCCGGCGGGCGCTGCGTGTGTGTTTG____TGCGAGTGTGAGTGAGTGTGAGTGCCGGG ACACT A LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:102114816..102114985 26863196 MeRIP-seq:(Medium) rs1190750956 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_861376,Human_RBP_ID_3938021,Human_RBP_ID_4137036,Human_RBP_ID_5280960,Human_RBP_ID_5313097,Human_RBP_ID_5520534,Human_RBP_ID_9321008,Human_RBP_ID_23112854,Human_RBP_ID_23430335,Human_RBP_ID_26316612 79811 RMVar_ID_79811 Human_SNP_ID_444702735 m1A Human chr10 - 102117550 102117550 102117550 AGGCACACTGGAGGCCTGGGTCAGGGAGCCCCAGGGGCCCGGGCAGGGGGCAGTGCTGGTACCTC AGGCACACTGGAGGCCTGGGTCAGGGAGCCCCTGGGGCCCGGGCAGGGGGCAGTGCTGGTACCTC T A LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102117539..102117706 26863196 MeRIP-seq:(Medium) rs990818769 Functional Loss SNV dbSNP153 33..33 33 - - - 79812 RMVar_ID_79812 Human_SNP_ID_444702739 m1A Human chr10 - 102117560 102117560 102117560 GAAGGGGGGCAGGCACACTGGAGGCCTGGGTCAGGGAGCCCCAGGGGCCCGGGCAGGGGGCAGTG GAAGGGGGGCAGGCACACTGGAGGCCTGGGTCCGGGAGCCCCAGGGGCCCGGGCAGGGGGCAGTG T G LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102117557..102117696 26863196 MeRIP-seq:(Medium) rs1291481814 Functional Loss SNV dbSNP153 33..33 33 - - - 79813 RMVar_ID_79813 Human_SNP_ID_444702886 m1A Human chr10 - 102118104 102118104 102118104 CACAAGGAAGGCATGGCAGCATGTAGCAGTCCAGGCCCAAAGATTTCCCCCACCTTGAGCAGCCC CACAAGGAAGGCATGGCAGCATGTAGCAGTCCGGGCCCAAAGATTTCCCCCACCTTGAGCAGCCC T C LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102118102..102118334 26863196 MeRIP-seq:(Medium) rs1434947736 Functional Loss SNV dbSNP153 33..33 33 - - - 79814 RMVar_ID_79814 Human_SNP_ID_444703448 m1A Human chr10 - 102120247 102120231 102120247 CAGGCCCCTCGCCGCAGCCAGGGGCCGCCCGCACCGGGCCGAGGCCGGGCCGGGCCGGCGGCGAG CAGGCCCCTCGCCGCAGCCAGGGGCCGCCCGC________________GCCGGGCCGGCGGCGAG CCCGGCCTCGGCCCGGT C LDB1 Ensembl:ENSG00000198728 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:102120153..102120403 26863410 MeRIP-seq:(Medium) rs1158889966 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_4137037,Human_RBP_ID_5487418 79815 RMVar_ID_79815 Human_SNP_ID_444703454 m1A Human chr10 - 102120247 102120247 102120247 CAGGCCCCTCGCCGCAGCCAGGGGCCGCCCGCACCGGGCCGAGGCCGGGCCGGGCCGGCGGCGAG CAGGCCCCTCGCCGCAGCCAGGGGCCGCCCGCTCCGGGCCGAGGCCGGGCCGGGCCGGCGGCGAG T A LDB1 Ensembl:ENSG00000198728 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:102120153..102120403 26863410 MeRIP-seq:(Medium) rs890724937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137037,Human_RBP_ID_5487418 79816 RMVar_ID_79816 Human_SNP_ID_444707210 m1A Human chr10 - 102133195 102133195 102133195 TCTCACCTGCTCGCCGCCGCTCACAGCGCCCAAAGTCCCATACGGCGCTTGGCTTCGACTTCCCC TCTCACCTGCTCGCCGCCGCTCACAGCGCCCAGAGTCCCATACGGCGCTTGGCTTCGACTTCCCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:102133051..102133304 26863196 MeRIP-seq:(Medium) rs1269769406 Functional Loss SNV dbSNP153 33..33 33 - - - 79817 RMVar_ID_79817 Human_SNP_ID_444708973 m1A Human chr10 - 102139611 102139610 102139612 CATCCAGGAGCACAGGCCGGGGTCCAGGAGAGACCTGTCGCACCACAACTGGGATCTCCAGGTCA CATCCAGGAGCACAGGCCGGGGTCCAGGAGA__CCTGTCGCACCACAACTGGGATCTCCAGGTCA GTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102139560..102139798 26863196 MeRIP-seq:(Medium) rs1280352556 Functional Loss DEL dbSNP153 32..33 33 - - - 79818 RMVar_ID_79818 Human_SNP_ID_444708989 m1A Human chr10 + 102139651 102139651 102139651 GGACCCCGGCCTGTGCTCCTGGATGACTCGCTAGAGACTAGTTCTGCCTTGCAGCTGCTTATGCC GGACCCCGGCCTGTGCTCCTGGATGACTCGCTGGAGACTAGTTCTGCCTTGCAGCTGCTTATGCC A G PPRC1 Ensembl:ENSG00000148840 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102139601..102139801 26863196 MeRIP-seq:(Medium) rs147674343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225300,Human_RBP_ID_1440493,Human_RBP_ID_1758953,Human_RBP_ID_2186438,Human_RBP_ID_5919425,Human_RBP_ID_8324371,Human_RBP_ID_8756995,Human_RBP_ID_9274221,Human_RBP_ID_11240751,Human_RBP_ID_27189004 Human_miRNA_ID_1968553 RMVar_hsa_circ_102843,RMVar_hsa_circ_88616,RMVar_hsa_circ_363416,RMVar_hsa_circ_145882,RMVar_hsa_circ_267337,RMVar_hsa_circ_105594,RMVar_hsa_circ_145884,RMVar_hsa_circ_145885,RMVar_hsa_circ_121645,RMVar_hsa_circ_145886,RMVar_hsa_circ_145888 79819 RMVar_ID_79819 Human_SNP_ID_444709472 m1A Human chr10 + 102140905 102140905 102140905 CTGGCAGACATCCCTTGTCTTGTCATCCCACCAGCCCCAGCCAAGAAGACAGCTCTGCAGAGAAG CTGGCAGACATCCCTTGTCTTGTCATCCCACCGGCCCCAGCCAAGAAGACAGCTCTGCAGAGAAG A G PPRC1 Ensembl:ENSG00000148840 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102140856..102141048 26863196 MeRIP-seq:(Medium) rs765093622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27622,Human_RBP_ID_368493,Human_RBP_ID_3938576,Human_RBP_ID_22030348 RMVar_hsa_circ_102843,RMVar_hsa_circ_88616,RMVar_hsa_circ_363416,RMVar_hsa_circ_145882,RMVar_hsa_circ_267337,RMVar_hsa_circ_105594,RMVar_hsa_circ_145884,RMVar_hsa_circ_145885,RMVar_hsa_circ_121645,RMVar_hsa_circ_145886,RMVar_hsa_circ_145888 79820 RMVar_ID_79820 Human_SNP_ID_444709565 m1A Human chr10 - 102141160 102141160 102141160 GGTGGGGGCAGACTGGGGGGCATGCCAAGCCCACCTGCAGGGAAAGGCAGGGCAGCAGACATCGA GGTGGGGGCAGACTGGGGGGCATGCCAAGCCCCCCTGCAGGGAAAGGCAGGGCAGCAGACATCGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102141109..102141416 26863196 MeRIP-seq:(Medium) rs1476772926 Functional Loss SNV dbSNP153 33..33 33 - - - 79821 RMVar_ID_79821 Human_SNP_ID_444709637 m1A Human chr10 - 102141318 102141318 102141318 CAGACACTAGGGGCACCGTTGGTGGGGGGGGCAGGCAAGGATAGCCAGAAGGGGACACATGAGGA CAGACACTAGGGGCACCGTTGGTGGGGGGGGCCGGCAAGGATAGCCAGAAGGGGACACATGAGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:102141276..102141383;chr10:102141272..102141395 26863196 MeRIP-seq:(Medium) rs145091275 Functional Loss SNV dbSNP153 33..33 33 - - - 79822 RMVar_ID_79822 Human_SNP_ID_444710807 m1A Human chr10 + 102144963 102144963 102144963 CACCCCCTCCCATTGATTTCTGAGAAAGGCAAATGTATAAGATATTGAGAAGGCAATGAATCAGG CACCCCCTCCCATTGATTTCTGAGAAAGGCAATTGTATAAGATATTGAGAAGGCAATGAATCAGG A T PPRC1 Ensembl:ENSG00000148840 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102144941..102145006 26863196 MeRIP-seq:(Medium) rs1416519926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27627,Human_RBP_ID_2186447,Human_RBP_ID_11240947 RMVar_hsa_circ_363416,RMVar_hsa_circ_145882,RMVar_hsa_circ_105594,RMVar_hsa_circ_145885,RMVar_hsa_circ_91534,RMVar_hsa_circ_121645,RMVar_hsa_circ_283581,RMVar_hsa_circ_145888,RMVar_hsa_circ_346639,RMVar_hsa_circ_101885,RMVar_hsa_circ_145889,RMVar_hsa_circ_145890,RMVar_hsa_circ_145891,RMVar_hsa_circ_59617,RMVar_hsa_circ_347040 79823 RMVar_ID_79823 Human_SNP_ID_444711501 m1A Human chr10 + 102147083 102147083 102147083 GCTTGATCACAGGACTAGCAGTGAGCAGGCAGATCCCTCAGCACCCTGCCTTGCCCCATCCAGCT GCTTGATCACAGGACTAGCAGTGAGCAGGCAGGTCCCTCAGCACCCTGCCTTGCCCCATCCAGCT A G PPRC1 Ensembl:ENSG00000148840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102147032..102147220 26863196 MeRIP-seq:(Medium) rs916845402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_981127,Human_RBP_ID_5138377,Human_RBP_ID_5919480,Human_RBP_ID_8324391,Human_RBP_ID_11241010,Human_RBP_ID_27189050 RMVar_hsa_circ_363416,RMVar_hsa_circ_145882,RMVar_hsa_circ_105594,RMVar_hsa_circ_145885,RMVar_hsa_circ_91534,RMVar_hsa_circ_121645,RMVar_hsa_circ_145888,RMVar_hsa_circ_346639,RMVar_hsa_circ_101885,RMVar_hsa_circ_21825,RMVar_hsa_circ_145890,RMVar_hsa_circ_145891,RMVar_hsa_circ_59617,RMVar_hsa_circ_34381 79824 RMVar_ID_79824 Human_SNP_ID_444711512 m1A Human chr10 - 102147109 102147109 102147109 GCAGGGTGAGGCCTCAGGGGACAGCAAGCTGGATGGGGCAAGGCAGGGTGCTGAGGGATCTGCCT GCAGGGTGAGGCCTCAGGGGACAGCAAGCTGGGTGGGGCAAGGCAGGGTGCTGAGGGATCTGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102147059..102147135 26863196 MeRIP-seq:(Medium) rs1406988010 Functional Loss SNV dbSNP153 33..33 33 - - - 79825 RMVar_ID_79825 Human_SNP_ID_444714656 m1A Human chr10 - 102157525 102157525 102157525 ACCTGGACAGGCTGTTTCTTTTGGTCCTCCTCATCATCATCATCACTGGACTCTTCACTGCTGCT ACCTGGACAGGCTGTTTCTTTTGGTCCTCCTCCTCATCATCATCACTGGACTCTTCACTGCTGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102157476..102157525 26863196 MeRIP-seq:(Medium) rs139625185 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9594 79826 RMVar_ID_79826 Human_SNP_ID_444714857 m1A Human chr10 + 102158191 102158191 102158191 GCCAAAGATAACACCTGTGACAGTTAAAGCTCAGACTAAAGCCCCTCCCAAACCAGGTACTGTTT GCCAAAGATAACACCTGTGACAGTTAAAGCTCCGACTAAAGCCCCTCCCAAACCAGGTACTGTTT A C NOLC1 Ensembl:ENSG00000166197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102158026..102158254 26863196 MeRIP-seq:(Medium) rs1195013633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27994,Human_RBP_ID_292327,Human_RBP_ID_981134,Human_RBP_ID_1440561,Human_RBP_ID_3336873,Human_RBP_ID_5919539,Human_RBP_ID_8981576,Human_RBP_ID_11241432,Human_RBP_ID_26802280 Human_Splice_Rec_1170845,Human_Splice_Rec_1170869,Human_Splice_Rec_1170891,Human_Splice_Rec_1170915,Human_Splice_Rec_1170949,Human_Splice_Rec_1170963,Human_Splice_Rec_1170977 Human_miRNA_ID_2390293,Human_miRNA_ID_2390294,Human_miRNA_ID_2591527,Human_miRNA_ID_2591528 RMVar_hsa_circ_5385,RMVar_hsa_circ_119556,RMVar_hsa_circ_88972,RMVar_hsa_circ_114225,RMVar_hsa_circ_145893,RMVar_hsa_circ_145894,RMVar_hsa_circ_274709,RMVar_hsa_circ_145896,RMVar_hsa_circ_29144,RMVar_hsa_circ_145895,RMVar_hsa_circ_98235,RMVar_hsa_circ_145897,RMVar_hsa_circ_101261,RMVar_hsa_circ_84948,RMVar_hsa_circ_145898,RMVar_hsa_circ_145899 79827 RMVar_ID_79827 Human_SNP_ID_444715347 m1A Human chr10 + 102159567 102159567 102159567 GAGGAGCAAAAAAAACCCATGAAAAATAAACCAGGTGACTGGACATGGGGAGCGAAGCTGTGTGA GAGGAGCAAAAAAAACCCATGAAAAATAAACCGGGTGACTGGACATGGGGAGCGAAGCTGTGTGA A G NOLC1 Ensembl:ENSG00000166197 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:102159416..102159577;chr10:102159426..102159575 26863196 MeRIP-seq:(Medium) rs1413621641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19045766 Human_Splice_Rec_1170849,Human_Splice_Rec_1170873,Human_Splice_Rec_1170895,Human_Splice_Rec_1170919,Human_Splice_Rec_1170935,Human_Splice_Rec_1170953,Human_Splice_Rec_1170967,Human_Splice_Rec_1170981 RMVar_hsa_circ_119556,RMVar_hsa_circ_88972,RMVar_hsa_circ_145894,RMVar_hsa_circ_145896,RMVar_hsa_circ_29144,RMVar_hsa_circ_98235,RMVar_hsa_circ_145897,RMVar_hsa_circ_101261,RMVar_hsa_circ_84948,RMVar_hsa_circ_145898,RMVar_hsa_circ_117180,RMVar_hsa_circ_367951,RMVar_hsa_circ_145899,RMVar_hsa_circ_118045,RMVar_hsa_circ_145900,RMVar_hsa_circ_145901 79828 RMVar_ID_79828 Human_SNP_ID_444715491 m1A Human chr10 + 102159965 102159965 102159965 ACCAAAGAAGTCTCTGGGAACCCAGCCTCCCAAGAAGGCTGTGGAGAAGCAGCAGCCTGTGGAAA ACCAAAGAAGTCTCTGGGAACCCAGCCTCCCAGGAAGGCTGTGGAGAAGCAGCAGCCTGTGGAAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1383040216 Functional Loss SNV dbSNP153 33..33 33 - - - 79829 RMVar_ID_79829 Human_SNP_ID_444715578 m1A Human chr10 - 102160229 102160229 102160229 GGGTTTCTTCTCTTCTTCAGAACTTGAATCTGAGGAGAACCTGTAGCATTATGCTGGGTCCAGAG GGGTTTCTTCTCTTCTTCAGAACTTGAATCTGCGGAGAACCTGTAGCATTATGCTGGGTCCAGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102160226..102160275 26863196 MeRIP-seq:(Medium) rs1564971077 Functional Loss SNV dbSNP153 33..33 33 - - - 79830 RMVar_ID_79830 Human_SNP_ID_444732774 m1A Human chr10 + 102230714 102230714 102230714 CGCGGCGGCGGCGGCGGCCGAGGCATAAGGGCAGGACACGGCCCCGGAGGACACGGCGGCCGGAG CGCGGCGGCGGCGGCGGCCGAGGCATAAGGGCGGGACACGGCCCCGGAGGACACGGCGGCCGGAG A G lnc-ELOVL3-1 RNACentral:URS00008BDF5B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102230665..102230904 26863196 MeRIP-seq:(Medium) rs1408808489 Functional Loss SNV dbSNP153 33..33 33 - - - 79831 RMVar_ID_79831 Human_SNP_ID_444732839 m1A Human chr10 + 102230863 102230863 102230863 TGGAGGCGGCGATGGAGCTGGGTGGCGAGAAGACGGGCTGCGAAGCCAGAGGCCCCACGTTGACC TGGAGGCGGCGATGGAGCTGGGTGGCGAGAAGGCGGGCTGCGAAGCCAGAGGCCCCACGTTGACC A G lnc-ELOVL3-1 RNACentral:URS00008BDF5B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102230607..102231626 26863196 MeRIP-seq:(Medium) rs771971140 Functional Loss SNV dbSNP153 33..33 33 - - - 79832 RMVar_ID_79832 Human_SNP_ID_444763963 m1A Human chr10 + 102365521 102365521 102365521 CAACACAGAGGTTGCTCAGTGGCTCCGAGAGAACCCTCGGCTGGACAAGAAGATGATTGGAGAGT CAACACAGAGGTTGCTCAGTGGCTCCGAGAGAGCCCTCGGCTGGACAAGAAGATGATTGGAGAGT A G GBF1 Ensembl:ENSG00000107862 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102365399..102365600 26863196 MeRIP-seq:(Medium) rs532707284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11243815,Human_RBP_ID_23430662,Human_RBP_ID_27802970 Human_Splice_Rec_1171051,Human_Splice_Rec_1171131,Human_Splice_Rec_1171209 RMVar_hsa_circ_93134,RMVar_hsa_circ_145909,RMVar_hsa_circ_265907,RMVar_hsa_circ_66484,RMVar_hsa_circ_145913,RMVar_hsa_circ_81558,RMVar_hsa_circ_109294,RMVar_hsa_circ_145914,RMVar_hsa_circ_113836,RMVar_hsa_circ_322644,RMVar_hsa_circ_272261,RMVar_hsa_circ_97598,RMVar_hsa_circ_27695,RMVar_hsa_circ_18302,RMVar_hsa_circ_4157,RMVar_hsa_circ_100359,RMVar_hsa_circ_145916,RMVar_hsa_circ_145917,RMVar_hsa_circ_145918,RMVar_hsa_circ_364035,RMVar_hsa_circ_145923,RMVar_hsa_circ_54698,RMVar_hsa_circ_290739,RMVar_hsa_circ_145921,RMVar_hsa_circ_281314,RMVar_hsa_circ_12751,RMVar_hsa_circ_145922,RMVar_hsa_circ_377879,RMVar_hsa_circ_91871,RMVar_hsa_circ_101493,RMVar_hsa_circ_22543,RMVar_hsa_circ_145926,RMVar_hsa_circ_145927 79833 RMVar_ID_79833 Human_SNP_ID_444768251 m1A Human chr10 - 102382179 102382179 102382179 CCTGCAGTGGGGAGGCCAAGGGCTGCAGGATCAGTGGGGGCTGAGCCAAGGGTGGAGGCCCGTCG CCTGCAGTGGGGAGGCCAAGGGCTGCAGGATCGGTGGGGGCTGAGCCAAGGGTGGAGGCCCGTCG T C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102382128..102382299 26863196 MeRIP-seq:(Medium) rs1461651426 Functional Loss SNV dbSNP153 33..33 33 - - - 79834 RMVar_ID_79834 Human_SNP_ID_444768252 m1A Human chr10 - 102382179 102382179 102382179 CCTGCAGTGGGGAGGCCAAGGGCTGCAGGATCAGTGGGGGCTGAGCCAAGGGTGGAGGCCCGTCG CCTGCAGTGGGGAGGCCAAGGGCTGCAGGATCCGTGGGGGCTGAGCCAAGGGTGGAGGCCCGTCG T G L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102382128..102382299 26863196 MeRIP-seq:(Medium) rs1461651426 Functional Loss SNV dbSNP153 33..33 33 - - - 79835 RMVar_ID_79835 Human_SNP_ID_444768262 m1A Human chr10 + 102382204 102382204 102382204 CCCCCACTGATCCTGCAGCCCTTGGCCTCCCCACTGCAGGTGGGCGTGCCACCTATGACTCTGCC CCCCCACTGATCCTGCAGCCCTTGGCCTCCCCGCTGCAGGTGGGCGTGCCACCTATGACTCTGCC A G GBF1 Ensembl:ENSG00000107862 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:102382051..102382325 26863410 MeRIP-seq:(Medium) rs954660813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8324538 RMVar_hsa_circ_91871,RMVar_hsa_circ_145927,RMVar_hsa_circ_145937 79836 RMVar_ID_79836 Human_SNP_ID_444768406 m1A Human chr10 - 102382628 102382628 102382628 GCCTGACCGTGGGCAGGCACTGCAGGGCCGGCACACGGATGCCTCCCCAGAGCTGCCGGGCTGGA GCCTGACCGTGGGCAGGCACTGCAGGGCCGGCGCACGGATGCCTCCCCAGAGCTGCCGGGCTGGA T C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102382583..102382672 26863196 MeRIP-seq:(Medium) rs1177133532 Functional Loss SNV dbSNP153 33..33 33 - - - 79837 RMVar_ID_79837 Human_SNP_ID_444768410 m1A Human chr10 + 102382651 102382651 102382651 GCATCCGTGTGCCGGCCCTGCAGTGCCTGCCCACGGTCAGGCATTGAAAACTAAGCCCAACCACT GCATCCGTGTGCCGGCCCTGCAGTGCCTGCCCCCGGTCAGGCATTGAAAACTAAGCCCAACCACT A C GBF1 Ensembl:ENSG00000107862 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:102382601..102382675 32194978 MeRIP-seq:(Medium) rs1470623865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18585708 RMVar_hsa_circ_91871,RMVar_hsa_circ_145927 79838 RMVar_ID_79838 Human_SNP_ID_444771795 m1A Human chr10 - 102395752 102395752 102395752 CCTGTCCGGGTGTGGCGGGTGAGATCCGGTGGAGAGCGAGATCCGGAGTTGGGCTTGGCCGGGGA CCTGTCCGGGTGTGGCGGGTGAGATCCGGTGGCGAGCGAGATCCGGAGTTGGGCTTGGCCGGGGA T G L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102395701..102396000 26863196 MeRIP-seq:(Medium) rs1313884048 Functional Loss SNV dbSNP153 33..33 33 - - - 79839 RMVar_ID_79839 Human_SNP_ID_444771797 m1A Human chr10 - 102395763 102395763 102395763 TCCTCCAGCCGCCTGTCCGGGTGTGGCGGGTGAGATCCGGTGGAGAGCGAGATCCGGAGTTGGGC TCCTCCAGCCGCCTGTCCGGGTGTGGCGGGTGGGATCCGGTGGAGAGCGAGATCCGGAGTTGGGC T C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102395737..102395821 26863196 MeRIP-seq:(Medium) rs1565203442 Functional Loss SNV dbSNP153 33..33 33 - - - 79840 RMVar_ID_79840 Human_SNP_ID_444771798 m1A Human chr10 + 102395765 102395765 102395765 CCAACTCCGGATCTCGCTCTCCACCGGATCTCACCCGCCACACCCGGACAGGCGGCTGGAGGAGG CCAACTCCGGATCTCGCTCTCCACCGGATCTCCCCCGCCACACCCGGACAGGCGGCTGGAGGAGG A C NFKB2 Ensembl:ENSG00000077150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102395715..102395938 26863196 MeRIP-seq:(Medium) rs1458040585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1171389,Human_Splice_Rec_1171433,Human_Splice_Rec_1171477 79841 RMVar_ID_79841 Human_SNP_ID_444774133 m1A Human chr10 + 102402360 102402360 102402360 GCCACCAGGAGGGCTCTGCCACGGGCACCCCCAGCCTCAGGTGCACTGACCTGCTGCCTGCCCCC GCCACCAGGAGGGCTCTGCCACGGGCACCCCCGGCCTCAGGTGCACTGACCTGCTGCCTGCCCCC A G NFKB2 Ensembl:ENSG00000077150 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102402310..102402416 26863196 MeRIP-seq:(Medium) rs1333059741 Functional Loss SNV dbSNP153 33..33 33 - - - 79842 RMVar_ID_79842 Human_SNP_ID_444780658 m1A Human chr10 - 102424159 102424157 102424160 TTTGTACCCTTAGGCAACTGGCGCTGAGGAGGAGCTTCTGCCAGGGGTGGATGTACTCCTGGAGG TTTGTACCCTTAGGCAACTGGCGCTGAGGAG___CTTCTGCCAGGGGTGGATGTACTCCTGGAGG GCTC G CUEDC2 Ensembl:ENSG00000107874 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:102423976..102424187 32194978 MeRIP-seq:(Medium) rs760646761 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_368673,Human_RBP_ID_981184,Human_RBP_ID_4104091,Human_RBP_ID_8324550,Human_RBP_ID_8757174,Human_RBP_ID_17768262,Human_RBP_ID_23123295 Human_Splice_Rec_1171700,Human_Splice_Rec_1171714 RMVar_hsa_circ_78286,RMVar_hsa_circ_114512,RMVar_hsa_circ_88663,RMVar_hsa_circ_145945,RMVar_hsa_circ_145943,RMVar_hsa_circ_145944 79843 RMVar_ID_79843 Human_SNP_ID_444781516 m1A Human chr10 + 102427453 102427453 102427453 TTTTACAGGCATCTCACAGTTAGCGTGTCCCAAACTAATGTTCTCTCAAGTGCTTTACTCCTCCA TTTTACAGGCATCTCACAGTTAGCGTGTCCCACACTAATGTTCTCTCAAGTGCTTTACTCCTCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102427451..102427900 26863196 MeRIP-seq:(Medium) rs781069311 Functional Loss SNV dbSNP153 33..33 33 - - - 79844 RMVar_ID_79844 Human_SNP_ID_444782802 m1A Human chr10 + 102432575 102432575 102432575 GCCGGCGACTTGTCCCGCGCGGTGCAGCTCTCATCCCCCAGCCCCACCAACGAGATCAAAGGCGG GCCGGCGACTTGTCCCGCGCGGTGCAGCTCTCGTCCCCCAGCCCCACCAACGAGATCAAAGGCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:102432472..102432643;chr10:102432475..102432659;chr10:102432462..102432600;chr10:102432465..102432600 26863196 MeRIP-seq:(Medium) rs1394697133 Functional Loss SNV dbSNP153 33..33 33 - - - 79845 RMVar_ID_79845 Human_SNP_ID_444787855 m1A Human chr10 + 102450871 102450871 102450871 CAGGGTCGTGGCGTAGGCCGGAGGGCAGGCCCACCAGGGCGGCGCGGCCTCGGGTGGCGCGGCGG CAGGGTCGTGGCGTAGGCCGGAGGGCAGGCCCTCCAGGGCGGCGCGGCCTCGGGTGGCGCGGCGG A T RPARP-AS1 Ensembl:ENSG00000269609 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102450669..102451007 26863196 MeRIP-seq:(Medium) rs1303502096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225587,Human_RBP_ID_22566665 RMVar_hsa_circ_94988,RMVar_hsa_circ_97803,RMVar_hsa_circ_145950,RMVar_hsa_circ_145951 79846 RMVar_ID_79846 Human_SNP_ID_444787920 m1A Human chr10 - 102450987 102450987 102450987 CCTGGCCGCCCCTCTGCTGCTACCCCCAGTCCAGGCCCACAGCTTCCGCAGCCGGCCCGGGAGCC CCTGGCCGCCCCTCTGCTGCTACCCCCAGTCCGGGCCCACAGCTTCCGCAGCCGGCCCGGGAGCC T C C10orf95 Ensembl:ENSG00000120055 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102450936..102451018 26863196 MeRIP-seq:(Medium) rs1299476303 Functional Loss SNV dbSNP153 33..33 33 - - - 79847 RMVar_ID_79847 Human_SNP_ID_444795783 m1A Human chr10 + 102479386 102479386 102479386 GCAGTCCGCGGGGCGCTACGTTGCTTTCACACATACCTGCTGCTGTGGCCCACACCTGGCAGGGG GCAGTCCGCGGGGCGCTACGTTGCTTTCACACGTACCTGCTGCTGTGGCCCACACCTGGCAGGGG A G NONHSAG006759.2 RNACentral:URS00008C1E5F lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102479335..102479464 26863196 MeRIP-seq:(Medium) rs1008765468 Functional Loss SNV dbSNP153 33..33 33 - - - 79848 RMVar_ID_79848 Human_SNP_ID_444795831 m1A Human chr10 + 102479627 102479627 102479627 CACTCTGGTCTGGCCCACTCCCTCCTTAACCAAGCAGGTCCAAGGTCAAGAATGGCACAAGATCA CACTCTGGTCTGGCCCACTCCCTCCTTAACCAGGCAGGTCCAAGGTCAAGAATGGCACAAGATCA A G NONHSAG006759.2 RNACentral:URS00008C1E5F lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:102479576..102479650 32194978 MeRIP-seq:(Medium) rs542729359 Functional Loss SNV dbSNP153 33..33 33 - - - 79849 RMVar_ID_79849 Human_SNP_ID_444795911 m1A Human chr10 + 102480059 102480059 102480059 GCAAGGCAGGAGGCAGCAAGCTCCCTCTCTCCAGCCCCTAACTGAACAAACACTTCAATAAATAA GCAAGGCAGGAGGCAGCAAGCTCCCTCTCTCCGGCCCCTAACTGAACAAACACTTCAATAAATAA A G NONHSAG006759.2 RNACentral:URS00008C1E5F lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:102479851..102480125 32194978 MeRIP-seq:(Medium) rs1449060429 Functional Loss SNV dbSNP153 33..33 33 - - - 79850 RMVar_ID_79850 Human_SNP_ID_444798386 m1A Human chr10 - 102490529 102490529 102490529 GCTTTCCAAACTAGTAAGTCATTCTGTAGCTTAGACGTTTTGGAGGCTCATCAGCTTTGTTACAG GCTTTCCAAACTAGTAAGTCATTCTGTAGCTTGGACGTTTTGGAGGCTCATCAGCTTTGTTACAG T C ACTR1A Ensembl:ENSG00000138107 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:102490526..102490625 32194978 MeRIP-seq:(Medium) rs760358772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11244622,Human_RBP_ID_24456009 Human_Splice_Rec_1171812,Human_Splice_Rec_1171826,Human_Splice_Rec_1171852 RMVar_hsa_circ_115422,RMVar_hsa_circ_145964,RMVar_hsa_circ_122736,RMVar_hsa_circ_79016,RMVar_hsa_circ_145965,RMVar_hsa_circ_145966,RMVar_hsa_circ_280015,RMVar_hsa_circ_116859,RMVar_hsa_circ_145973,RMVar_hsa_circ_145974 79851 RMVar_ID_79851 Human_SNP_ID_444798387 m1A Human chr10 - 102490529 102490529 102490529 GCTTTCCAAACTAGTAAGTCATTCTGTAGCTTAGACGTTTTGGAGGCTCATCAGCTTTGTTACAG GCTTTCCAAACTAGTAAGTCATTCTGTAGCTTCGACGTTTTGGAGGCTCATCAGCTTTGTTACAG T G ACTR1A Ensembl:ENSG00000138107 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:102490526..102490625 32194978 MeRIP-seq:(Medium) rs760358772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11244622,Human_RBP_ID_24456009 Human_Splice_Rec_1171812,Human_Splice_Rec_1171826,Human_Splice_Rec_1171852 RMVar_hsa_circ_115422,RMVar_hsa_circ_145964,RMVar_hsa_circ_122736,RMVar_hsa_circ_79016,RMVar_hsa_circ_145965,RMVar_hsa_circ_145966,RMVar_hsa_circ_280015,RMVar_hsa_circ_116859,RMVar_hsa_circ_145973,RMVar_hsa_circ_145974 79852 RMVar_ID_79852 Human_SNP_ID_444801301 m1A Human chr10 + 102502651 102502651 102502651 TGGTTGGCGATCACATCGTAGGACTCCATGGCAGAGGAATCTCTCCTTCTGGGGAAGGAACTGCC TGGTTGGCGATCACATCGTAGGACTCCATGGCGGAGGAATCTCTCCTTCTGGGGAAGGAACTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102502561..102502654 26863196 MeRIP-seq:(Medium) rs764315656 Functional Loss SNV dbSNP153 33..33 33 - - - 79853 RMVar_ID_79853 Human_SNP_ID_444801718 m1A Human chr10 + 102504060 102504060 102504060 TAGACCTCGCTGCAGCCCCCATCGCCTCGGGGAGTCTCACCCACCGAGTCCGCCCGCTGGCCCGT TAGACCTCGCTGCAGCCCCCATCGCCTCGGGGTGTCTCACCCACCGAGTCCGCCCGCTGGCCCGT A T SUFU Ensembl:ENSG00000107882 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102504027..102504234 26863196 MeRIP-seq:(Medium) rs1393750028 Functional Loss SNV dbSNP153 33..33 33 - - - 79854 RMVar_ID_79854 Human_SNP_ID_444801746 m1A Human chr10 - 102504124 102504124 102504124 CCATCGGGGTGCGTAGGGCAGGCACTGGGGGAACTGGAGAGGGCAAACGACGGGGAGAGCACTGA CCATCGGGGTGCGTAGGGCAGGCACTGGGGGATCTGGAGAGGGCAAACGACGGGGAGAGCACTGA T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:102504029..102504225 26863410 MeRIP-seq:(Medium) rs1267745109 Functional Loss SNV dbSNP153 33..33 33 - - - 79855 RMVar_ID_79855 Human_SNP_ID_444801763 m1A Human chr10 - 102504163 102504163 102504163 GCGCGGTGGGGCCGGGGGCGCCGCTAGGCCGCAGCTCCGCCATCGGGGTGCGTAGGGCAGGCACT GCGCGGTGGGGCCGGGGGCGCCGCTAGGCCGCCGCTCCGCCATCGGGGTGCGTAGGGCAGGCACT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102504026..102504228 26863196 MeRIP-seq:(Medium) rs1297525468 Functional Loss SNV dbSNP153 33..33 33 - - - 79856 RMVar_ID_79856 Human_SNP_ID_444816177 m1A Human chr10 + 102563426 102563426 102563426 GGCGAGGGCTCAGGAAAAGCTGGAGGCCTGGCAAGAATAGGAAAGTGCTGGGCTTGAGGCAAGTC GGCGAGGGCTCAGGAAAAGCTGGAGGCCTGGCCAGAATAGGAAAGTGCTGGGCTTGAGGCAAGTC A C SUFU Ensembl:ENSG00000107882 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102563393..102563506 26863196 MeRIP-seq:(Medium) rs1181903804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145975,RMVar_hsa_circ_109981 79857 RMVar_ID_79857 Human_SNP_ID_444835601 m1A Human chr10 - 102643005 102643004 102643005 GTCGCCTCAGAGCTTTATCCTCAGATCAAAAAAGAAAAAACAGGAAGAAAAAAATCCCAACCCCA GTCGCCTCAGAGCTTTATCCTCAGATCAAAAA_GAAAAAACAGGAAGAAAAAAATCCCAACCCCA CT C AL391121.1 Ensembl:ENSG00000272933 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102642957..102643110 26863196 MeRIP-seq:(Medium) rs1564716864 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5092809 79858 RMVar_ID_79858 Human_SNP_ID_444835607 m1A Human chr10 + 102643038 102643038 102643038 TTTTTGATCTGAGGATAAAGCTCTGAGGCGACAGCGGCTGCGGAGACCCTGCCCGAAGCGCCCTC TTTTTGATCTGAGGATAAAGCTCTGAGGCGACGGCGGCTGCGGAGACCCTGCCCGAAGCGCCCTC A G TRIM8 Ensembl:ENSG00000171206 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102642990..102643102 26863196 MeRIP-seq:(Medium) rs1260217115 Functional Loss SNV dbSNP153 33..33 33 - - - 79859 RMVar_ID_79859 Human_SNP_ID_444835877 m1A Human chr10 - 102643781 102643781 102643781 GGAGGGAGAAGCCCCGGCGGCGCTCCGGCCTGACCCCCGGGCGGCTACTTCTGCGCTCCCCCGAG GGAGGGAGAAGCCCCGGCGGCGCTCCGGCCTGGCCCCCGGGCGGCTACTTCTGCGCTCCCCCGAG T C AL391121.1 Ensembl:ENSG00000272933 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:102643690..102643791 26863410 MeRIP-seq:(Medium) rs1464096036 Functional Loss SNV dbSNP153 33..33 33 - - - 79860 RMVar_ID_79860 Human_SNP_ID_444835929 m1A Human chr10 + 102643938 102643938 102643938 CTCTGGCCGGGGACTGGAATTTCATCTGAATGACTGCCCCTGCGCGCACGCAGCGCCCCGGAGTC CTCTGGCCGGGGACTGGAATTTCATCTGAATGCCTGCCCCTGCGCGCACGCAGCGCCCCGGAGTC A C TRIM8 Ensembl:ENSG00000171206 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102643888..102644339 26863196 MeRIP-seq:(Medium) rs1295736788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4104401,Human_RBP_ID_27403539 79861 RMVar_ID_79861 Human_SNP_ID_444839961 m1A Human chr10 + 102657760 102657760 102657760 CACCCTTCTTACCCCACCCGGGAGGAACGCCCAGGGCCCCGGGCTTGTTTCTCCTCTTGTTTTCC CACCCTTCTTACCCCACCCGGGAGGAACGCCCGGGGCCCCGGGCTTGTTTCTCCTCTTGTTTTCC A G TRIM8 Ensembl:ENSG00000171206 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:102657709..102657876 26863196 MeRIP-seq:(Medium) rs879906547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225463,Human_RBP_ID_18931201 Human_miRNA_ID_2577297 RMVar_hsa_circ_88173,RMVar_hsa_circ_120284,RMVar_hsa_circ_145984,RMVar_hsa_circ_145987,RMVar_hsa_circ_145988,RMVar_hsa_circ_124728 79862 RMVar_ID_79862 Human_SNP_ID_444842892 m1A Human chr10 - 102667839 102667839 102667839 TTGTCTGACCTCATCACTTGCTACTCTCTCCCACCCCCAACACTTTCCAGCTGCCCTCGCCCCCT TTGTCTGACCTCATCACTTGCTACTCTCTCCCCCCCCCAACACTTTCCAGCTGCCCTCGCCCCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102667797..102667921 26863196 MeRIP-seq:(Medium) rs1269211358 Functional Loss SNV dbSNP153 33..33 33 - - - 79863 RMVar_ID_79863 Human_SNP_ID_444847132 m1A Human chr10 - 102685999 102685999 102685999 CTTCCCTCCCTCTCCCTTCTCAAAATCCAGGAACTAGCGGAATTACTGGAGGAAGAAAAACTAAG CTTCCCTCCCTCTCCCTTCTCAAAATCCAGGATCTAGCGGAATTACTGGAGGAAGAAAAACTAAG T A ARL3 Ensembl:ENSG00000138175 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102685948..102699450 26863196 MeRIP-seq:(Medium) rs538533205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8981682,Human_RBP_ID_26317461 Human_Splice_Rec_1172080 RMVar_hsa_circ_47564,RMVar_hsa_circ_311573,RMVar_hsa_circ_331122,RMVar_hsa_circ_269956,RMVar_hsa_circ_145989,RMVar_hsa_circ_145990,RMVar_hsa_circ_145991 79864 RMVar_ID_79864 Human_SNP_ID_444851971 m1A Human chr10 + 102705457 102705457 102705457 AGGAGAAGTATTCTCACCTCCTGGTCTGGTGCACTTTTCAACTTGCGCAAAATTGAGAGCAAGCC AGGAGAAGTATTCTCACCTCCTGGTCTGGTGCGCTTTTCAACTTGCGCAAAATTGAGAGCAAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102705406..102714360 26863196 MeRIP-seq:(Medium) rs1275507320 Functional Loss SNV dbSNP153 33..33 33 - - - 79865 RMVar_ID_79865 Human_SNP_ID_444851980 m1A Human chr10 + 102705486 102705486 102705486 TGCACTTTTCAACTTGCGCAAAATTGAGAGCAAGCCCTTCAACAACCACAAAGGAGACAGATTAC TGCACTTTTCAACTTGCGCAAAATTGAGAGCACGCCCTTCAACAACCACAAAGGAGACAGATTAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102705376..102714383 26863196 MeRIP-seq:(Medium) rs1276064080 Functional Loss SNV dbSNP153 33..33 33 - - - 79866 RMVar_ID_79866 Human_SNP_ID_444854358 m1A Human chr10 - 102714683 102714683 102714683 ACAGGGCGAGCGCCATTGTCCCAAGGCCCCTTACCTGGTCCCGGGACAAATGCCACCAGTTACAG ACAGGGCGAGCGCCATTGTCCCAAGGCCCCTTTCCTGGTCCCGGGACAAATGCCACCAGTTACAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:102714660..102714737;chr10:102714659..102714757 26863196 MeRIP-seq:(Medium) rs1396309112 Functional Loss SNV dbSNP153 33..33 33 - - - 79867 RMVar_ID_79867 Human_SNP_ID_444861240 m1A Human chr10 - 102743104 102743102 102743104 TTTTAAATACTTCATCTACCTACAGAATAGAGAGTCCAAACTTCCCAACACGGTCCTCTCTGTGA TTTTAAATACTTCATCTACCTACAGAATAGAG__TCCAAACTTCCCAACACGGTCCTCTCTGTGA ACT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102742980..102743208 26863196 MeRIP-seq:(Medium) rs938453747 Functional Loss DEL dbSNP153 33..34 33 - - - 79868 RMVar_ID_79868 Human_SNP_ID_444861502 m1A Human chr10 + 102744009 102744009 102744009 GAAGAGGGTAGAGGAGGAGAGGGAGGAGGAGGAGGGAGGTGGCGGCGCCGTGGCGGAGGAGCAGG GAAGAGGGTAGAGGAGGAGAGGGAGGAGGAGGGGGGAGGTGGCGGCGCCGTGGCGGAGGAGCAGG A G WBP1L Ensembl:ENSG00000166272 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102743959..102776274 26863196 MeRIP-seq:(Medium) rs1022530701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225928,Human_RBP_ID_4136030,Human_RBP_ID_9413174,Human_RBP_ID_26316639 79869 RMVar_ID_79869 Human_SNP_ID_444874353 m1A Human chr10 + 102797927 102797927 102797927 TGGGGGCTGGTGAATAGACAACCAGGAGGACAATGATGAGAAGGAAAGTGTTCAAAAGCTGTCAT TGGGGGCTGGTGAATAGACAACCAGGAGGACAGTGATGAGAAGGAAAGTGTTCAAAAGCTGTCAT A G WBP1L Ensembl:ENSG00000166272 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102797924..102798011 26863196 MeRIP-seq:(Medium) rs548948104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11246610 79870 RMVar_ID_79870 Human_SNP_ID_444900602 m1A Human chr10 + 102900922 102900921 102900922 CCTGGCCAACATGGTGAAATCCTGTCTCTACCAAAAATACAAAAAAAATTAGCTGGGCATGGTGG CCTGGCCAACATGGTGAAATCCTGTCTCTACC_AAAATACAAAAAAAATTAGCTGGGCATGGTGG CA C BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1455640191 Functional Loss DEL dbSNP153 33..33 33 - - - 79871 RMVar_ID_79871 Human_SNP_ID_444900603 m1A Human chr10 + 102900922 102900922 102900922 CCTGGCCAACATGGTGAAATCCTGTCTCTACCAAAAATACAAAAAAAATTAGCTGGGCATGGTGG CCTGGCCAACATGGTGAAATCCTGTCTCTACCTAAAATACAAAAAAAATTAGCTGGGCATGGTGG A T BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs185693154 Functional Loss SNV dbSNP153 33..33 33 - - - 79872 RMVar_ID_79872 Human_SNP_ID_444904968 m1A Human chr10 + 102918371 102918371 102918371 TGAGGTGGAGTCAGTGTCAGTCAGGGAGGCGAACTGCTGAGCACTGGCCGCGGACGCTCCGTTGC TGAGGTGGAGTCAGTGTCAGTCAGGGAGGCGATCTGCTGAGCACTGGCCGCGGACGCTCCGTTGC A T CNNM2 Ensembl:ENSG00000148842 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102918340..102918550 26863196 MeRIP-seq:(Medium) rs555951352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137055,Human_RBP_ID_5520543,Human_RBP_ID_18468861 Clinvar_Rec_368 79873 RMVar_ID_79873 Human_SNP_ID_444905134 m1A Human chr10 + 102918672 102918672 102918672 CTGAGCTGCTGCTGCGGTGCGGGCGGCTGCGCAGCGGTGGGCGAGAATGAGGAGACGGTGATCAT CTGAGCTGCTGCTGCGGTGCGGGCGGCTGCGCCGCGGTGGGCGAGAATGAGGAGACGGTGATCAT A C CNNM2 Ensembl:ENSG00000148842 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:102918626..102918700 26863196 MeRIP-seq:(Medium) rs1366563473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137057,Human_RBP_ID_5520277 79874 RMVar_ID_79874 Human_SNP_ID_444912249 m1A Human chr10 - 102948407 102948406 102948408 TTACCTCCCACCTTATCATGTCTCCCTGCAATAGTCTCTTTTCCACACCCAAATTTCCTCTAGTT TTACCTCCCACCTTATCATGTCTCCCTGCAA__GTCTCTTTTCCACACCCAAATTTCCTCTAGTT CTA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102948313..102948412 26863196 MeRIP-seq:(Medium) rs1206417099 Functional Loss DEL dbSNP153 32..33 33 - - - 79875 RMVar_ID_79875 Human_SNP_ID_444946938 m1A Human chr10 - 103089666 103089666 103089666 GAAGAGGAGGAGGAGGAGGAAGAATAAGGAGGAAAACCAAAACCCCAAGCACCCATTAAACAAGT GAAGAGGAGGAGGAGGAGGAAGAATAAGGAGGGAAACCAAAACCCCAAGCACCCATTAAACAAGT T C NT5C2 Ensembl:ENSG00000076685 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:103089615..103089752;chr10:103089617..103089726 26863196 MeRIP-seq:(Medium) rs769565424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22887084,Human_RBP_ID_26317462 RMVar_hsa_circ_146018,RMVar_hsa_circ_84668 79876 RMVar_ID_79876 Human_SNP_ID_444946939 m1A Human chr10 - 103089666 103089666 103089666 GAAGAGGAGGAGGAGGAGGAAGAATAAGGAGGAAAACCAAAACCCCAAGCACCCATTAAACAAGT GAAGAGGAGGAGGAGGAGGAAGAATAAGGAGGCAAACCAAAACCCCAAGCACCCATTAAACAAGT T G NT5C2 Ensembl:ENSG00000076685 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:103089615..103089752;chr10:103089617..103089726 26863196 MeRIP-seq:(Medium) rs769565424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22887084,Human_RBP_ID_26317462 RMVar_hsa_circ_146018,RMVar_hsa_circ_84668 79877 RMVar_ID_79877 Human_SNP_ID_444972734 m1A Human chr10 + 103192706 103192706 103192706 CTGCTAAAACGCTGTCAACCTGGCGCTCCACCAGAGGCCCCTTGGCTTCTCGGGAGGCGACCGAG CTGCTAAAACGCTGTCAACCTGGCGCTCCACCGGAGGCCCCTTGGCTTCTCGGGAGGCGACCGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103192702..103193258 26863196 MeRIP-seq:(Medium) rs1233812864 Functional Loss SNV dbSNP153 33..33 33 - - - 79878 RMVar_ID_79878 Human_SNP_ID_444972774 m1A Human chr10 - 103192807 103192807 103192807 CTCAGTCCTGCTGACGTCCTCCAGCTGATTCCAGGCTGTTCCCGGCCACCCCTGAGGCCGTCTTT CTCAGTCCTGCTGACGTCCTCCAGCTGATTCCGGGCTGTTCCCGGCCACCCCTGAGGCCGTCTTT T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:103192805..103193107 26863196 MeRIP-seq:(Medium) rs1407686893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146035 79879 RMVar_ID_79879 Human_SNP_ID_444972909 m1A Human chr10 - 103193062 103193062 103193062 CAAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCAGCGCGCTCGCGGACGCCGCACGCCTCCCAACT CAAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCTGCGCGCTCGCGGACGCCGCACGCCTCCCAACT T A NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:103192788..103193207 26863196 MeRIP-seq:(Medium) rs1327133007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5340174 RMVar_hsa_circ_146035 79880 RMVar_ID_79880 Human_SNP_ID_444972910 m1A Human chr10 - 103193062 103193062 103193062 CAAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCAGCGCGCTCGCGGACGCCGCACGCCTCCCAACT CAAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCGGCGCGCTCGCGGACGCCGCACGCCTCCCAACT T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:103192788..103193207 26863196 MeRIP-seq:(Medium) rs1327133007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5340174 RMVar_hsa_circ_146035 79881 RMVar_ID_79881 Human_SNP_ID_444972927 m1A Human chr10 - 103193093 103193093 103193093 CCCCGCCCCCGGCCCCCAGGGACCATGGCCCCAAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCAG CCCCGCCCCCGGCCCCCAGGGACCATGGCCCCGAGGCCCCTCTCCTTAGGCCGAGTCCCCGCCAG T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:103193086..103193186 32194978 MeRIP-seq:(Medium) rs1324851315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146035 79882 RMVar_ID_79882 Human_SNP_ID_445013367 m1A Human chr10 - 103350729 103350729 103350729 TCACTTCTCGTTGAGGCTGGAGGGAGGCCGGCAGGACTCGGAGGACGAGGAGGAGGTATTTAGAG TCACTTCTCGTTGAGGCTGGAGGGAGGCCGGCTGGACTCGGAGGACGAGGAGGAGGTATTTAGAG T A PCGF6 Ensembl:ENSG00000156374 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:103348977..103350904;chr10:103348933..103350900 26863196 MeRIP-seq:(Medium) rs1392380317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225358,Human_RBP_ID_5921717,Human_RBP_ID_9360736,Human_RBP_ID_26317464 Human_Splice_Rec_1172681,Human_Splice_Rec_1172693,Human_Splice_Rec_1172711,Human_Splice_Rec_1172729 RMVar_hsa_circ_108777,RMVar_hsa_circ_146049,RMVar_hsa_circ_97500,RMVar_hsa_circ_124946,RMVar_hsa_circ_146055,RMVar_hsa_circ_146056 79883 RMVar_ID_79883 Human_SNP_ID_445013551 m1A Human chr10 + 103351032 103351032 103351032 AGGCTGCAGCTCCCTCGGTTTTGGCAGCGCCTACGCTGCCCGCCGTCACCACCGCGACCCCCTCC AGGCTGCAGCTCCCTCGGTTTTGGCAGCGCCTGCGCTGCCCGCCGTCACCACCGCGACCCCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103350984..103351110 26863196 MeRIP-seq:(Medium) rs1411009380 Functional Loss SNV dbSNP153 33..33 33 - - - 79884 RMVar_ID_79884 Human_SNP_ID_445013553 m1A Human chr10 - 103351036 103351036 103351036 CCATGGAGGGGGTCGCGGTGGTGACGGCGGGCAGCGTAGGCGCTGCCAAAACCGAGGGAGCTGCA CCATGGAGGGGGTCGCGGTGGTGACGGCGGGCGGCGTAGGCGCTGCCAAAACCGAGGGAGCTGCA T C PCGF6 Ensembl:ENSG00000156374 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:103350985..103351085;chr10:103350985..103351096 26863196 MeRIP-seq:(Medium) rs1421164322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4105012 RMVar_hsa_circ_108777,RMVar_hsa_circ_146049,RMVar_hsa_circ_97500,RMVar_hsa_circ_124946,RMVar_hsa_circ_146055,RMVar_hsa_circ_146056 79885 RMVar_ID_79885 Human_SNP_ID_445018276 m1A Human chr10 + 103368034 103368034 103368034 GCGGAGGAGCAGACGGAGGTGGCGGTCAAGCTAGAGCCTGAGGGACCGCCAACGCTGCTACCTCC GCGGAGGAGCAGACGGAGGTGGCGGTCAAGCTGGAGCCTGAGGGACCGCCAACGCTGCTACCTCC A G TAF5 Ensembl:ENSG00000148835 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:103367989..103373370 26863196 MeRIP-seq:(Medium) rs1164015539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_369057,Human_RBP_ID_4105028 RMVar_hsa_circ_92893,RMVar_hsa_circ_146057 79886 RMVar_ID_79886 Human_SNP_ID_445018348 m1A Human chr10 - 103368231 103368216 103368231 GCGGAGCGCCGGCGTCCGGAGCAGCGGCGGGCACCGGGGCCGCCCCCGCCGGGGCAGCGGCGGAG GCGGAGCGCCGGCGTCCGGAGCAGCGGCGGGC_______________GCCGGGGCAGCGGCGGAG CGGGGGCGGCCCCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:103368193..103368375 26863196 MeRIP-seq:(Medium) rs1261720144 Functional Loss DEL dbSNP153 33..47 33 - - - 79887 RMVar_ID_79887 Human_SNP_ID_445018354 m1A Human chr10 - 103368231 103368231 103368231 GCGGAGCGCCGGCGTCCGGAGCAGCGGCGGGCACCGGGGCCGCCCCCGCCGGGGCAGCGGCGGAG GCGGAGCGCCGGCGTCCGGAGCAGCGGCGGGCGCCGGGGCCGCCCCCGCCGGGGCAGCGGCGGAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:103368193..103368375 26863196 MeRIP-seq:(Medium) rs1270244844 Functional Loss SNV dbSNP153 33..33 33 - - - 79888 RMVar_ID_79888 Human_SNP_ID_445019998 m1A Human chr10 + 103373866 103373866 103373866 GTAGGAGTTAACCAGATGAAGAGAAGAGGGAAAAGCATGTGTAAAAGCTCTCTGGTGGGAAGGAT GTAGGAGTTAACCAGATGAAGAGAAGAGGGAATAGCATGTGTAAAAGCTCTCTGGTGGGAAGGAT A T TAF5 Ensembl:ENSG00000148835 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:103373749..103373878 26863196 MeRIP-seq:(Medium) rs1480178895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17183015 RMVar_hsa_circ_64161,RMVar_hsa_circ_92893,RMVar_hsa_circ_146057,RMVar_hsa_circ_341822,RMVar_hsa_circ_300126,RMVar_hsa_circ_146058,RMVar_hsa_circ_146059 79889 RMVar_ID_79889 Human_SNP_ID_445024463 m1A Human chr10 - 103392223 103392223 103392223 CATTGATTGTCTTATATTTCAAGTTAAGGTCCAAAAAAACTCCAGCTGTGAAAGCAACATAAATG CATTGATTGTCTTATATTTCAAGTTAAGGTCCGAAAAAACTCCAGCTGTGAAAGCAACATAAATG T C ATP5MD Ensembl:ENSG00000173915 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755540729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273535,Human_RBP_ID_1440884,Human_RBP_ID_1759333,Human_RBP_ID_3337408,Human_RBP_ID_8981792,Human_RBP_ID_9321017,Human_RBP_ID_17229523,Human_RBP_ID_17648188,Human_RBP_ID_22752515,Human_RBP_ID_24777528,Human_RBP_ID_27189479 Human_Splice_Rec_1172776,Human_Splice_Rec_1172777,Human_Splice_Rec_1172782,Human_Splice_Rec_1172783,Human_Splice_Rec_1172788,Human_Splice_Rec_1172789,Human_Splice_Rec_1172796,Human_Splice_Rec_1172797,Human_Splice_Rec_1172804,Human_Splice_Rec_1172805 RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146067,RMVar_hsa_circ_376067,RMVar_hsa_circ_146064,RMVar_hsa_circ_285584,RMVar_hsa_circ_146066 79890 RMVar_ID_79890 Human_SNP_ID_445031331 m1A Human chr10 - 103418490 103418490 103418490 GGGAGGAAAGCACGGATGTTGTGGGGCAGGACAGCCACCTCCAGCCCATCTTTGGTCTTCTCTAA GGGAGGAAAGCACGGATGTTGTGGGGCAGGACGGCCACCTCCAGCCCATCTTTGGTCTTCTCTAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103418401..103418536 26863196 MeRIP-seq:(Medium) rs780255626 Functional Loss SNV dbSNP153 33..33 33 - - - 79891 RMVar_ID_79891 Human_SNP_ID_445036977 m1A Human chr10 + 103440495 103440489 103440495 AGAAGAACCAGAAGGGGCAGGAGGAGGTGGAGATGCCCAGCAAGGAGAAGCAACAGCCCCAGAAG AGAAGAACCAGAAGGGGCAGGAGGAGG______TGCCCAGCAAGGAGAAGCAACAGCCCCAGAAG GTGGAGA G PDCD11 Ensembl:ENSG00000148843 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:103440451..103440745 26863196 MeRIP-seq:(Medium) rs749196197 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_862822,Human_RBP_ID_9360745,Human_RBP_ID_17648078,Human_RBP_ID_22886915,Human_RBP_ID_24542128,Human_RBP_ID_26316649,Human_RBP_ID_27802328 Human_Splice_Rec_1172863,Human_Splice_Rec_1172933 RMVar_hsa_circ_122085,RMVar_hsa_circ_146081,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_112152,RMVar_hsa_circ_87500,RMVar_hsa_circ_75702,RMVar_hsa_circ_123259,RMVar_hsa_circ_146108,RMVar_hsa_circ_146107,RMVar_hsa_circ_146109,RMVar_hsa_circ_41162,RMVar_hsa_circ_146110,RMVar_hsa_circ_118625,RMVar_hsa_circ_79305,RMVar_hsa_circ_81441,RMVar_hsa_circ_101824,RMVar_hsa_circ_44329,RMVar_hsa_circ_146113,RMVar_hsa_circ_115505,RMVar_hsa_circ_146117,RMVar_hsa_circ_146118,RMVar_hsa_circ_146116,RMVar_hsa_circ_112872,RMVar_hsa_circ_278684,RMVar_hsa_circ_127567,RMVar_hsa_circ_146121,RMVar_hsa_circ_146123,RMVar_hsa_circ_146122,RMVar_hsa_circ_146120 79892 RMVar_ID_79892 Human_SNP_ID_445036987 m1A Human chr10 + 103440508 103440508 103440508 GGGGCAGGAGGAGGTGGAGATGCCCAGCAAGGAGAAGCAACAGCCCCAGAAGCCACAGGCGCAGA GGGGCAGGAGGAGGTGGAGATGCCCAGCAAGGGGAAGCAACAGCCCCAGAAGCCACAGGCGCAGA A G PDCD11 Ensembl:ENSG00000148843 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:103440501..103440525 26863196 MeRIP-seq:(Medium) rs1339961634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862822,Human_RBP_ID_9360745,Human_RBP_ID_17648078,Human_RBP_ID_22886915,Human_RBP_ID_24542128,Human_RBP_ID_26316649,Human_RBP_ID_26767723,Human_RBP_ID_27802328 Human_Splice_Rec_1172863,Human_Splice_Rec_1172933 RMVar_hsa_circ_122085,RMVar_hsa_circ_146081,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_112152,RMVar_hsa_circ_87500,RMVar_hsa_circ_75702,RMVar_hsa_circ_123259,RMVar_hsa_circ_146108,RMVar_hsa_circ_146107,RMVar_hsa_circ_146109,RMVar_hsa_circ_41162,RMVar_hsa_circ_146110,RMVar_hsa_circ_118625,RMVar_hsa_circ_79305,RMVar_hsa_circ_81441,RMVar_hsa_circ_101824,RMVar_hsa_circ_44329,RMVar_hsa_circ_146113,RMVar_hsa_circ_115505,RMVar_hsa_circ_146117,RMVar_hsa_circ_146118,RMVar_hsa_circ_146116,RMVar_hsa_circ_112872,RMVar_hsa_circ_278684,RMVar_hsa_circ_127567,RMVar_hsa_circ_146121,RMVar_hsa_circ_146123,RMVar_hsa_circ_146122,RMVar_hsa_circ_146120 79893 RMVar_ID_79893 Human_SNP_ID_445037076 m1A Human chr10 + 103440746 103440746 103440746 TCTCCCACCTGGCCTCTCAGGAAAGAGTGAGCAAGAAGCCAAAGAAAGCCGGCCTGTCAGAGGAG TCTCCCACCTGGCCTCTCAGGAAAGAGTGAGCCAGAAGCCAAAGAAAGCCGGCCTGTCAGAGGAG A C PDCD11 Ensembl:ENSG00000148843 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:103440387..103442023;chr10:103440351..103442425;chr10:103440350..103442400 26863196 MeRIP-seq:(Medium) rs1466449308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27678,Human_RBP_ID_191972,Human_RBP_ID_9360747,Human_RBP_ID_19577072,Human_RBP_ID_26316651 Human_Splice_Rec_1172864,Human_Splice_Rec_1172934 RMVar_hsa_circ_122085,RMVar_hsa_circ_146081,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_112152,RMVar_hsa_circ_87500,RMVar_hsa_circ_75702,RMVar_hsa_circ_123259,RMVar_hsa_circ_146108,RMVar_hsa_circ_146107,RMVar_hsa_circ_146109,RMVar_hsa_circ_41162,RMVar_hsa_circ_146110,RMVar_hsa_circ_118625,RMVar_hsa_circ_79305,RMVar_hsa_circ_81441,RMVar_hsa_circ_101824,RMVar_hsa_circ_44329,RMVar_hsa_circ_146113,RMVar_hsa_circ_115505,RMVar_hsa_circ_146117,RMVar_hsa_circ_146118,RMVar_hsa_circ_146116,RMVar_hsa_circ_112872,RMVar_hsa_circ_278684,RMVar_hsa_circ_146121,RMVar_hsa_circ_146122,RMVar_hsa_circ_146120 79894 RMVar_ID_79894 Human_SNP_ID_445037126 m1A Human chr10 - 103440884 103440884 103440884 GCAGAGGATGGCCCAGCTCTTCCCTTGCCTGGAGCAGCCTTCCCCTCCCCGCGACGTCACCCTCA GCAGAGGATGGCCCAGCTCTTCCCTTGCCTGGTGCAGCCTTCCCCTCCCCGCGACGTCACCCTCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103440685..103440884 26863196 MeRIP-seq:(Medium) rs1041505502 Functional Loss SNV dbSNP153 33..33 33 - - - 79895 RMVar_ID_79895 Human_SNP_ID_445037342 m1A Human chr10 - 103441795 103441795 103441795 TCCTGGAGGAACACAGAGGCGCTAAAGAAAGCACCTGGCTCAGGCTGCTCCCTGTTCCCCCGTGC TCCTGGAGGAACACAGAGGCGCTAAAGAAAGCCCCTGGCTCAGGCTGCTCCCTGTTCCCCCGTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103441791..103442005 26863196 MeRIP-seq:(Medium) rs1363658909 Functional Loss SNV dbSNP153 33..33 33 - - - 79896 RMVar_ID_79896 Human_SNP_ID_445039759 m1A Human chr10 + 103449977 103449977 103449977 GATAGTCGTGGCGGGGTGGATTGCAGGAGAGGAGGCAGGAGGAGACGGGATTGATGGTTGCTGGT GATAGTCGTGGCGGGGTGGATTGCAGGAGAGGCGGCAGGAGGAGACGGGATTGATGGTTGCTGGT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103449966..103450051 26863196 MeRIP-seq:(Medium) rs772076601 Functional Loss SNV dbSNP153 33..33 33 - - - 79897 RMVar_ID_79897 Human_SNP_ID_445072170 m1A Human chr10 + 103585097 103585097 103585097 GCACAGCGGCGACATCCTGGGCCTGGTGGTCAACGCCGACGGCGAGCTGCACCTCAGCCACAATG GCACAGCGGCGACATCCTGGGCCTGGTGGTCAGCGCCGACGGCGAGCTGCACCTCAGCCACAATG A G NEURL1 Ensembl:ENSG00000107954 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:103585051..103585265;chr10:103585046..103585350 26863196 MeRIP-seq:(Medium) rs1174253659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18586140 RMVar_hsa_circ_146129,RMVar_hsa_circ_274853,RMVar_hsa_circ_146128 79898 RMVar_ID_79898 Human_SNP_ID_445072192 m1A Human chr10 + 103585127 103585127 103585127 CAACGCCGACGGCGAGCTGCACCTCAGCCACAATGGCGCGGCCGCCGGCATGCAGCTGTGCGTGG CAACGCCGACGGCGAGCTGCACCTCAGCCACAGTGGCGCGGCCGCCGGCATGCAGCTGTGCGTGG A G NEURL1 Ensembl:ENSG00000107954 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:103585076..103585227 26863196 MeRIP-seq:(Medium) rs779154530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18586140 Human_Splice_Rec_1173015 RMVar_hsa_circ_146129,RMVar_hsa_circ_274853,RMVar_hsa_circ_146128 79899 RMVar_ID_79899 Human_SNP_ID_445072240 m1A Human chr10 - 103585227 103585227 103585227 AGGCATACGCCCAGGCGCAGCTGCGGGCACTCACCGAGGATGCGGATCTGCGTGATGGTCCCGTG AGGCATACGCCCAGGCGCAGCTGCGGGCACTCGCCGAGGATGCGGATCTGCGTGATGGTCCCGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:103585051..103585291 26863196 MeRIP-seq:(Medium) rs111783293 Functional Loss SNV dbSNP153 33..33 33 - - - 79900 RMVar_ID_79900 Human_SNP_ID_445073531 m1A Human chr10 - 103590114 103590114 103590114 TTGGGGGCTGTCCCTGAGGACAAGGGGGCACCAGTCAGGAGGAGACATGGCCCAACCCGGCGCTG TTGGGGGCTGTCCCTGAGGACAAGGGGGCACCGGTCAGGAGGAGACATGGCCCAACCCGGCGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:103590111..103590406 26863196 MeRIP-seq:(Medium) rs374755992 Functional Loss SNV dbSNP153 33..33 33 - - - 79901 RMVar_ID_79901 Human_SNP_ID_445077377 m1A Human chr10 - 103603594 103603594 103603594 CCAAGGAGGCCGAGGAGGGCCCTACGGGGGCCAGTGAGAGCCAGGACTCCCCGCGGAAGCTCAAG CCAAGGAGGCCGAGGAGGGCCCTACGGGGGCCCGTGAGAGCCAGGACTCCCCGCGGAAGCTCAAG T G SH3PXD2A Ensembl:ENSG00000107957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103603546..103603733 26863196 MeRIP-seq:(Medium) rs1193408799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520305,Human_RBP_ID_27189621 79902 RMVar_ID_79902 Human_SNP_ID_445086028 m1A Human chr10 - 103637983 103637983 103637983 TCTGACCAGGGGAGGCCTGGCCGAGGGTGGGCAGCCTTTCACTGGTCTTAAAGGCACAGCACTCG TCTGACCAGGGGAGGCCTGGCCGAGGGTGGGCGGCCTTTCACTGGTCTTAAAGGCACAGCACTCG T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:103637979..103638092 26863196 MeRIP-seq:(Medium) rs7910092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364900 RMVar_hsa_circ_35758,RMVar_hsa_circ_324517,RMVar_hsa_circ_291291,RMVar_hsa_circ_71694,RMVar_hsa_circ_344284,RMVar_hsa_circ_290916,RMVar_hsa_circ_19664,RMVar_hsa_circ_310670 79903 RMVar_ID_79903 Human_SNP_ID_445088931 m1A Human chr10 + 103650473 103650473 103650473 AAGGCCCTTCAAAGCCCTTGACCAGTTCCTCCAGCTTCTCTCAGGCAGCCCCCAGGCACTGTGGC AAGGCCCTTCAAAGCCCTTGACCAGTTCCTCCGGCTTCTCTCAGGCAGCCCCCAGGCACTGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103650470..103650661 26863196 MeRIP-seq:(Medium) rs368461744 Functional Loss SNV dbSNP153 33..33 33 - - - 79904 RMVar_ID_79904 Human_SNP_ID_445098873 m1A Human chr10 - 103693119 103693119 103693119 ACCGACCGCAGCCAGCCCGAGGGCGCCCCTGCAGCTGCAGCCCCGCGCTCGCGCCCGGCCCTAAC ACCGACCGCAGCCAGCCCGAGGGCGCCCCTGCTGCTGCAGCCCCGCGCTCGCGCCCGGCCCTAAC T A SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103693068..103693161 26863196 MeRIP-seq:(Medium) rs747312565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4105458 Human_Splice_Rec_1173045,Human_Splice_Rec_1173073,Human_Splice_Rec_1173093,Human_Splice_Rec_1173119 RMVar_hsa_circ_71694,RMVar_hsa_circ_19664,RMVar_hsa_circ_108199,RMVar_hsa_circ_41233,RMVar_hsa_circ_146136 79905 RMVar_ID_79905 Human_SNP_ID_445098874 m1A Human chr10 - 103693119 103693119 103693119 ACCGACCGCAGCCAGCCCGAGGGCGCCCCTGCAGCTGCAGCCCCGCGCTCGCGCCCGGCCCTAAC ACCGACCGCAGCCAGCCCGAGGGCGCCCCTGCCGCTGCAGCCCCGCGCTCGCGCCCGGCCCTAAC T G SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103693068..103693161 26863196 MeRIP-seq:(Medium) rs747312565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4105458 Human_Splice_Rec_1173045,Human_Splice_Rec_1173073,Human_Splice_Rec_1173093,Human_Splice_Rec_1173119 RMVar_hsa_circ_71694,RMVar_hsa_circ_19664,RMVar_hsa_circ_108199,RMVar_hsa_circ_41233,RMVar_hsa_circ_146136 79906 RMVar_ID_79906 Human_SNP_ID_445098879 m1A Human chr10 - 103693132 103693132 103693132 AGCGGCACCGGGGACCGACCGCAGCCAGCCCGAGGGCGCCCCTGCAGCTGCAGCCCCGCGCTCGC AGCGGCACCGGGGACCGACCGCAGCCAGCCCGGGGGCGCCCCTGCAGCTGCAGCCCCGCGCTCGC T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103693025..103693178 26863196 MeRIP-seq:(Medium) rs1426133451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71694,RMVar_hsa_circ_19664,RMVar_hsa_circ_108199,RMVar_hsa_circ_41233,RMVar_hsa_circ_146136 79907 RMVar_ID_79907 Human_SNP_ID_445137210 m1A Human chr10 - 103855331 103855304 103855331 GGCGGCCCCGGGACCCCGGCAGCTGGAGAAGGAGCCGGAGCCCGGCCGGGATGAGAAGGTGACGC GGCGGCCCCGGGACCCCGGCAGCTGGAGAAGG___________________________TGACGC ACCTTCTCATCCCGGCCGGGCTCCGGCT A SH3PXD2A Ensembl:ENSG00000107957 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103855282..103855535 26863196 MeRIP-seq:(Medium) rs750780548 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_862842,Human_RBP_ID_4136042,Human_RBP_ID_5340948,Human_RBP_ID_9361585 79908 RMVar_ID_79908 Human_SNP_ID_445137225 m1A Human chr10 - 103855351 103855351 103855351 CGCGCCGGGCCGGGGTGGCGGGCGGCCCCGGGACCCCGGCAGCTGGAGAAGGAGCCGGAGCCCGG CGCGCCGGGCCGGGGTGGCGGGCGGCCCCGGGTCCCCGGCAGCTGGAGAAGGAGCCGGAGCCCGG T A SH3PXD2A Ensembl:ENSG00000107957 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103855308..103855537 26863196 MeRIP-seq:(Medium) rs915475034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862842,Human_RBP_ID_4105483,Human_RBP_ID_5340948,Human_RBP_ID_18468826 79909 RMVar_ID_79909 Human_SNP_ID_445163977 m1A Human chr10 + 103967219 103967219 103967219 GAGGGAGACAGGCGGCGGCGGCGGCGCCCCAGACCCGAGGGGACGCGCGGGCCTTGCGCCGCGGG GAGGGAGACAGGCGGCGGCGGCGGCGCCCCAGTCCCGAGGGGACGCGCGGGCCTTGCGCCGCGGG A T SLK Ensembl:ENSG00000065613 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:103967177..103967608 26863196 MeRIP-seq:(Medium) rs911324007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4137068,Human_RBP_ID_5340192,Human_RBP_ID_9321022,Human_RBP_ID_18416356 79910 RMVar_ID_79910 Human_SNP_ID_445164060 m1A Human chr10 + 103967493 103967493 103967493 CGGGCAGGTGCCGCTCCCGGAGGGTGGGCCGGAGGCGAGGCGCCCACCGCGCGGCTCGCGGGCCG CGGGCAGGTGCCGCTCCCGGAGGGTGGGCCGGGGGCGAGGCGCCCACCGCGCGGCTCGCGGGCCG A G SLK Ensembl:ENSG00000065613 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103967126..103967803 26863196 MeRIP-seq:(Medium) rs1442430413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225663,Human_RBP_ID_369268,Human_RBP_ID_805198,Human_RBP_ID_4136047,Human_RBP_ID_8228919,Human_RBP_ID_8765459,Human_RBP_ID_9273993,Human_RBP_ID_9321024,Human_RBP_ID_9361586,Human_RBP_ID_22030160 79911 RMVar_ID_79911 Human_SNP_ID_445172686 m1A Human chr10 + 104002777 104002777 104002777 ACAAAGGAAGACACCCAAGAGAAATTGGGGGAAGACGACAAAACTCAAAAAGATGTGATCAGCAA ACAAAGGAAGACACCCAAGAGAAATTGGGGGAGGACGACAAAACTCAAAAAGATGTGATCAGCAA A G SLK Ensembl:ENSG00000065613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:104002726..104003150;chr10:104002726..104003175 26863196 MeRIP-seq:(Medium) rs749056305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28504,Human_RBP_ID_225664,Human_RBP_ID_24542021,Human_RBP_ID_26316668 RMVar_hsa_circ_241,RMVar_hsa_circ_365591,RMVar_hsa_circ_36293,RMVar_hsa_circ_16733,RMVar_hsa_circ_146145,RMVar_hsa_circ_68533,RMVar_hsa_circ_55080,RMVar_hsa_circ_52633,RMVar_hsa_circ_354905,RMVar_hsa_circ_146146,RMVar_hsa_circ_30858 79912 RMVar_ID_79912 Human_SNP_ID_445180845 m1A Human chr10 + 104035859 104035859 104035859 TGTATGGGAGTGTATCGGAGTGTGCGTATGGGAGTGTATGGGAGTGTGCGTGAGTACTGGAGTGT TGTATGGGAGTGTATCGGAGTGTGCGTATGGGTGTGTATGGGAGTGTGCGTGAGTACTGGAGTGT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:104035807..104035926 26863196 MeRIP-seq:(Medium) rs1404680148 Functional Loss SNV dbSNP153 33..33 33 - - - 79913 RMVar_ID_79913 Human_SNP_ID_445180888 m1A Human chr10 + 104035897 104035897 104035897 TGGGAGTGTGCGTGAGTACTGGAGTGTATGGGAGCGTGTGTATGGGAGTGTGTATGAGTGTGTGT TGGGAGTGTGCGTGAGTACTGGAGTGTATGGGTGCGTGTGTATGGGAGTGTGTATGAGTGTGTGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:104035847..104035938 26863196 MeRIP-seq:(Medium) rs28375989 Functional Loss SNV dbSNP153 33..33 33 - - - 79914 RMVar_ID_79914 Human_SNP_ID_445181250 m1A Human chr10 - 104036199 104036194 104036200 CCATACACACACACCCATACTCACACTCCCATACACACACACACTCACTTCCATACACACACACC CCATACACACACACCCATACTCACACTCCCA______CACACACTCACTTCCATACACACACACC GTGTGTA G COL17A1 Ensembl:ENSG00000065618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:104035672..104036268 26863196 MeRIP-seq:(Medium) rs1419726324 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_146155,RMVar_hsa_circ_114837,RMVar_hsa_circ_120742,RMVar_hsa_circ_122756,RMVar_hsa_circ_126326,RMVar_hsa_circ_121774,RMVar_hsa_circ_116452,RMVar_hsa_circ_117065,RMVar_hsa_circ_116252,RMVar_hsa_circ_109441,RMVar_hsa_circ_114081,RMVar_hsa_circ_109260,RMVar_hsa_circ_97890,RMVar_hsa_circ_98868,RMVar_hsa_circ_96537,RMVar_hsa_circ_77300,RMVar_hsa_circ_82029,RMVar_hsa_circ_87484,RMVar_hsa_circ_89154,RMVar_hsa_circ_86743,RMVar_hsa_circ_80984,RMVar_hsa_circ_81124,RMVar_hsa_circ_79723,RMVar_hsa_circ_146163,RMVar_hsa_circ_146171,RMVar_hsa_circ_146173,RMVar_hsa_circ_146175,RMVar_hsa_circ_146176,RMVar_hsa_circ_146177,RMVar_hsa_circ_146174,RMVar_hsa_circ_146172,RMVar_hsa_circ_146169,RMVar_hsa_circ_146170,RMVar_hsa_circ_146168,RMVar_hsa_circ_146164,RMVar_hsa_circ_146159,RMVar_hsa_circ_146161,RMVar_hsa_circ_146162,RMVar_hsa_circ_146160,RMVar_hsa_circ_146157,RMVar_hsa_circ_146158,RMVar_hsa_circ_146156,RMVar_hsa_circ_93928,RMVar_hsa_circ_87861,RMVar_hsa_circ_146153,RMVar_hsa_circ_146154,RMVar_hsa_circ_109484,RMVar_hsa_circ_84885,RMVar_hsa_circ_119660,RMVar_hsa_circ_146178,RMVar_hsa_circ_146179,RMVar_hsa_circ_146181,RMVar_hsa_circ_115308,RMVar_hsa_circ_146180,RMVar_hsa_circ_104732,RMVar_hsa_circ_113223,RMVar_hsa_circ_146182,RMVar_hsa_circ_104316,RMVar_hsa_circ_146187,RMVar_hsa_circ_83311,RMVar_hsa_circ_92513,RMVar_hsa_circ_82396,RMVar_hsa_circ_75589,RMVar_hsa_circ_76387,RMVar_hsa_circ_146189,RMVar_hsa_circ_146191,RMVar_hsa_circ_146190,RMVar_hsa_circ_146188,RMVar_hsa_circ_146183,RMVar_hsa_circ_146185,RMVar_hsa_circ_146186,RMVar_hsa_circ_146184 79915 RMVar_ID_79915 Human_SNP_ID_445201981 m1A Human chr10 + 104122195 104122195 104122195 GCTTTTTTGCTCTCGCTGGGAATGGCGGAGGGAGGTACCCTGCTGAGGGGAAGGGGGGATCCCTG GCTTTTTTGCTCTCGCTGGGAATGGCGGAGGGGGGTACCCTGCTGAGGGGAAGGGGGGATCCCTG A G SFR1 Ensembl:ENSG00000156384 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:104122185..104122324 26863196 MeRIP-seq:(Medium) rs1299399322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19045835,Human_RBP_ID_24361524 Human_Splice_Rec_1173639 RMVar_hsa_circ_109357,RMVar_hsa_circ_146239 79916 RMVar_ID_79916 Human_SNP_ID_445201982 m1A Human chr10 - 104122198 104122198 104122198 TGTCAGGGATCCCCCCTTCCCCTCAGCAGGGTACCTCCCTCCGCCATTCCCAGCGAGAGCAAAAA TGTCAGGGATCCCCCCTTCCCCTCAGCAGGGTGCCTCCCTCCGCCATTCCCAGCGAGAGCAAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:104122192..104122315 26863196 MeRIP-seq:(Medium) rs901265764 Functional Loss SNV dbSNP153 33..33 33 - - - 79917 RMVar_ID_79917 Human_SNP_ID_445232890 m1A Human chr10 - 104254953 104254953 104254953 TCTTCGCGGCGGGCAGGCCTCACCCTTCCCCAAGCTCCTGGCTGACTCCCCGGACATCGTGGCGC TCTTCGCGGCGGGCAGGCCTCACCCTTCCCCAGGCTCCTGGCTGACTCCCCGGACATCGTGGCGC T C lnc-CFAP43-6 RNACentral:URS0000D5DD18 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:104254876..104255275;chr10:104254775..104255275;chr10:104254790..104255200;chr10:104254876..104255200 26863196 MeRIP-seq:(Medium) rs776806870 Functional Loss SNV dbSNP153 33..33 33 - - - 79918 RMVar_ID_79918 Human_SNP_ID_445232891 m1A Human chr10 - 104254953 104254953 104254953 TCTTCGCGGCGGGCAGGCCTCACCCTTCCCCAAGCTCCTGGCTGACTCCCCGGACATCGTGGCGC TCTTCGCGGCGGGCAGGCCTCACCCTTCCCCACGCTCCTGGCTGACTCCCCGGACATCGTGGCGC T G lnc-CFAP43-6 RNACentral:URS0000D5DD18 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:104254876..104255275;chr10:104254775..104255275;chr10:104254790..104255200;chr10:104254876..104255200 26863196 MeRIP-seq:(Medium) rs776806870 Functional Loss SNV dbSNP153 33..33 33 - - - 79919 RMVar_ID_79919 Human_SNP_ID_445232893 m1A Human chr10 + 104254960 104254960 104254960 GATGTCCGGGGAGTCAGCCAGGAGCTTGGGGAAGGGTGAGGCCTGCCCGCCGCGAAGAGGGGGTG GATGTCCGGGGAGTCAGCCAGGAGCTTGGGGAGGGGTGAGGCCTGCCCGCCGCGAAGAGGGGGTG A G GSTO1 Ensembl:ENSG00000148834 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:104254901..104254975 32194978 MeRIP-seq:(Medium) rs915721379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747506,Human_RBP_ID_864240,Human_RBP_ID_4136509,Human_RBP_ID_5313104,Human_RBP_ID_8765720,Human_RBP_ID_9320706,Human_RBP_ID_9360767,Human_RBP_ID_18187997,Human_RBP_ID_18416486,Human_RBP_ID_19045836,Human_RBP_ID_22426080,Human_RBP_ID_22432247 Human_Splice_Rec_1173887,Human_Splice_Rec_1173895 RMVar_hsa_circ_95362,RMVar_hsa_circ_146251 79920 RMVar_ID_79920 Human_SNP_ID_445233030 m1A Human chr10 - 104255250 104255250 104255250 TGGGTGCCCACCTGATTCCCTTGGCCTTCAGGACTAGACGCGTCCTCTCAGCAAACGGGCAGAAC TGGGTGCCCACCTGATTCCCTTGGCCTTCAGGGCTAGACGCGTCCTCTCAGCAAACGGGCAGAAC T C lnc-CFAP43-6 RNACentral:URS0000D5DD18 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:104255201..104255275 32194978 MeRIP-seq:(Medium) rs781512367 Functional Loss SNV dbSNP153 33..33 33 - - - 79921 RMVar_ID_79921 Human_SNP_ID_445246846 m1A Human chr10 + 104314529 104314529 104314529 AGTCCAGTGTCTTACGGTAAAGGCTTCGCTGCAGGACGAAGGGCCGGAAGAGGTTGAGGGGCTCG AGTCCAGTGTCTTACGGTAAAGGCTTCGCTGCGGGACGAAGGGCCGGAAGAGGTTGAGGGGCTCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:104314480..104314630 32194978 MeRIP-seq:(Medium) rs1264844314 Functional Loss SNV dbSNP153 33..33 33 - - - 79922 RMVar_ID_79922 Human_SNP_ID_445246963 m1A Human chr10 + 104314780 104314780 104314780 GTCTTCAGGTGGTAGCTGCTGAGCCCGCTGGGACCGGTCAGGCGGCTCTGCTTGGAGAGCAGGAA GTCTTCAGGTGGTAGCTGCTGAGCCCGCTGGGGCCGGTCAGGCGGCTCTGCTTGGAGAGCAGGAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:104314729..104314830 32194978 MeRIP-seq:(Medium) rs752976549 Functional Loss SNV dbSNP153 33..33 33 - - - 79923 RMVar_ID_79923 Human_SNP_ID_445246964 m1A Human chr10 + 104314780 104314780 104314780 GTCTTCAGGTGGTAGCTGCTGAGCCCGCTGGGACCGGTCAGGCGGCTCTGCTTGGAGAGCAGGAA GTCTTCAGGTGGTAGCTGCTGAGCCCGCTGGGTCCGGTCAGGCGGCTCTGCTTGGAGAGCAGGAA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:104314729..104314830 32194978 MeRIP-seq:(Medium) rs752976549 Functional Loss SNV dbSNP153 33..33 33 - - - 79924 RMVar_ID_79924 Human_SNP_ID_445247461 m1A Human chr10 - 104315858 104315858 104315858 CCTGGAGGAGGAGGTGGCTCGGCTGGCGGCCGAAAAGGAGGCACTGGAGCAGGTGGCGGAGGAGG CCTGGAGGAGGAGGTGGCTCGGCTGGCGGCCGGAAAGGAGGCACTGGAGCAGGTGGCGGAGGAGG T C ITPRIP Ensembl:ENSG00000148841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:104315720..104316005 26863196 MeRIP-seq:(Medium) rs1241430245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4105896,Human_RBP_ID_5137930,Human_RBP_ID_22029549 RMVar_hsa_circ_104371,RMVar_hsa_circ_146258,RMVar_hsa_circ_93051,RMVar_hsa_circ_146257 79925 RMVar_ID_79925 Human_SNP_ID_445251392 m1A Human chr10 - 104333310 104333310 104333310 CACAGGTGTGTTTCTCAGAGGCTGGGGAGAGGATGGGCCCAGTTAGCGGCAGGGTGAATAGAAGA CACAGGTGTGTTTCTCAGAGGCTGGGGAGAGGTTGGGCCCAGTTAGCGGCAGGGTGAATAGAAGA T A ITPRIP Ensembl:ENSG00000148841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:104333303..104333372 26863196 MeRIP-seq:(Medium) rs549835391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104371,RMVar_hsa_circ_146258 79926 RMVar_ID_79926 Human_SNP_ID_445252650 m1A Human chr10 - 104338404 104338404 104338404 AGCCGGCCGCTGCAGGCCAGAAGGTGGGAGCCAGCGGGGGCATCGCCGCCCGCGCCCCTCTAAGT AGCCGGCCGCTGCAGGCCAGAAGGTGGGAGCCCGCGGGGGCATCGCCGCCCGCGCCCCTCTAAGT T G ITPRIP Ensembl:ENSG00000148841 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:104338130..104338425;chr10:104338178..104338475 26863196 MeRIP-seq:(Medium) rs1190684085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104371,RMVar_hsa_circ_146258 79927 RMVar_ID_79927 Human_SNP_ID_654948548 m1A Human chr19 - 199269 199172 199270 TCACACCGGCCCCTCCCACGCTGAGAGAGGTCAGCGTGAGCCCCTTGTCTCACACCGGCCCCTCC TCACACCGGCCCCTCCCACGCTGAGAGAGGT__________________________________ CACCTCTCTCAGCGTGGGAGGGGCCGGTGTGAGGCAAGGGGCTCGGGCTGACCTCTCTCAGCGTGGGAGGGGCCGGTGTGAGACAAGGGGCTCACGCTG C LINC01002 Ensembl:ENSG00000282508 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1568174276 Functional Loss DEL dbSNP153 32..65 33 - - - 79928 RMVar_ID_79928 Human_SNP_ID_654948575 m1A Human chr19 - 199269 199266 199270 TCACACCGGCCCCTCCCACGCTGAGAGAGGTCAGCGTGAGCCCCTTGTCTCACACCGGCCCCTCC TCACACCGGCCCCTCCCACGCTGAGAGAGGT____GTGAGCCCCTTGTCTCACACCGGCCCCTCC CGCTG C LINC01002 Ensembl:ENSG00000282508 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1346334101 Functional Loss DEL dbSNP153 32..35 33 - - - 79929 RMVar_ID_79929 Human_SNP_ID_654948840 m1A Human chr19 - 200317 200317 200317 TGAGAGAGGTCAGAGTGAGCCCCTTGTCTCACACCGGCCCCTCCCACGTGGACAGAGGTCAGCGT TGAGAGAGGTCAGAGTGAGCCCCTTGTCTCACCCCGGCCCCTCCCACGTGGACAGAGGTCAGCGT T G LINC01002 Ensembl:ENSG00000282508 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1352539805 Functional Loss SNV dbSNP153 33..33 33 - - - 79930 RMVar_ID_79930 Human_SNP_ID_654967234 m1A Human chr19 + 287600 287600 287600 CGGCTAGGAAGTTGGGCCTCAGACGCCCAATCATGTACTTGGCCAGGTCTGTCAGAGACTGGCTC CGGCTAGGAAGTTGGGCCTCAGACGCCCAATCGTGTACTTGGCCAGGTCTGTCAGAGACTGGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:287550..287798 26863196 MeRIP-seq:(Medium) rs371103775 Functional Loss SNV dbSNP153 33..33 33 - - - 79931 RMVar_ID_79931 Human_SNP_ID_654967235 m1A Human chr19 + 287600 287600 287600 CGGCTAGGAAGTTGGGCCTCAGACGCCCAATCATGTACTTGGCCAGGTCTGTCAGAGACTGGCTC CGGCTAGGAAGTTGGGCCTCAGACGCCCAATCTTGTACTTGGCCAGGTCTGTCAGAGACTGGCTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:287550..287798 26863196 MeRIP-seq:(Medium) rs371103775 Functional Loss SNV dbSNP153 33..33 33 - - - 79932 RMVar_ID_79932 Human_SNP_ID_654967476 m1A Human chr19 - 288127 288127 288127 TCGCTATCCTGACGCTGGTGAACGCCCCGTACAAGCGAGGATTTTACTGCGGGGATGACTCCATC TCGCTATCCTGACGCTGGTGAACGCCCCGTACGAGCGAGGATTTTACTGCGGGGATGACTCCATC T C PLPP2 Ensembl:ENSG00000141934 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:288076..288175 32194978 MeRIP-seq:(Medium) rs1032579315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27466499 Human_Splice_Rec_1928080,Human_Splice_Rec_1928090,Human_Splice_Rec_1928100,Human_Splice_Rec_1928114,Human_Splice_Rec_1928128 RMVar_hsa_circ_16902 79933 RMVar_ID_79933 Human_SNP_ID_654967480 m1A Human chr19 + 288130 288130 288130 GGAGTCATCCCCGCAGTAAAATCCTCGCTTGTACGGGGCGTTCACCAGCGTCAGGATAGCGAAGG GGAGTCATCCCCGCAGTAAAATCCTCGCTTGTGCGGGGCGTTCACCAGCGTCAGGATAGCGAAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:288081..288205 26863196 MeRIP-seq:(Medium) rs1254484959 Functional Loss SNV dbSNP153 33..33 33 - - - 79934 RMVar_ID_79934 Human_SNP_ID_654967492 m1A Human chr19 - 288154 288154 288154 TTTCTTCCCCACCAGCCTCCCTGCCCTTCGCTATCCTGACGCTGGTGAACGCCCCGTACAAGCGA TTTCTTCCCCACCAGCCTCCCTGCCCTTCGCTGTCCTGACGCTGGTGAACGCCCCGTACAAGCGA T C PLPP2 Ensembl:ENSG00000141934 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:287969..288206 26863196 MeRIP-seq:(Medium) rs1343676228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928080,Human_Splice_Rec_1928090,Human_Splice_Rec_1928100,Human_Splice_Rec_1928114,Human_Splice_Rec_1928128 RMVar_hsa_circ_16902 79935 RMVar_ID_79935 Human_SNP_ID_654974255 m1A Human chr19 + 307403 307403 307403 TATGAGGCTGGGTCGGCCAGGGCTGGGGGCCGATGGGACAGGGGTACAGCGGGGGACTCATCCAG TATGAGGCTGGGTCGGCCAGGGCTGGGGGCCGGTGGGACAGGGGTACAGCGGGGGACTCATCCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:307352..307472 26863196 MeRIP-seq:(Medium) rs775907843 Functional Loss SNV dbSNP153 33..33 33 - - - 79936 RMVar_ID_79936 Human_SNP_ID_654975218 m1A Human chr19 + 309744 309744 309744 ACGCACACAAGGCTTCAGGGACACGAGAAGGGACACACACACACGCACACAAGGCTTCAGGGAGA ACGCACACAAGGCTTCAGGGACACGAGAAGGGTCACACACACACGCACACAAGGCTTCAGGGAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:309716..309791 26863196 MeRIP-seq:(Medium) rs1234890108 Functional Loss SNV dbSNP153 33..33 33 - - - 79937 RMVar_ID_79937 Human_SNP_ID_654982130 m1A Human chr19 - 329121 329121 329121 GGAGGCCAGTGCTAACATCTTGAGAGAATGAGAGGGAGTGTTCCGGAAGTTGGAAGCTGAAAGTG GGAGGCCAGTGCTAACATCTTGAGAGAATGAGGGGGAGTGTTCCGGAAGTTGGAAGCTGAAAGTG T C MIER2 Ensembl:ENSG00000105556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:329119..329207 26863196 MeRIP-seq:(Medium) rs1170580162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8482828 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850 79938 RMVar_ID_79938 Human_SNP_ID_654983684 m1A Human chr19 - 334458 334458 334458 ACAGAACTACAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCAGACAAGCCCAAGGAGG ACAGAACTACAGTGTTAGGGGGGAGTGCGAGGCGGCCTCGAGGTGCCCAGACAAGCCCAAGGAGG T G MIER2 Ensembl:ENSG00000105556 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:334359..334466 26863196 MeRIP-seq:(Medium) rs1383703516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909859,Human_RBP_ID_18995527,Human_RBP_ID_19088236 Human_Splice_Rec_1928138,Human_Splice_Rec_1928139,Human_Splice_Rec_1928168,Human_Splice_Rec_1928169,Human_Splice_Rec_1928178,Human_Splice_Rec_1928179,Human_Splice_Rec_1928184,Human_Splice_Rec_1928185,Human_Splice_Rec_1928192,Human_Splice_Rec_1928193,Human_Splice_Rec_1928198 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850,RMVar_hsa_circ_190851,RMVar_hsa_circ_270394 79939 RMVar_ID_79939 Human_SNP_ID_654983694 m1A Human chr19 - 334474 334473 334474 TCGCAGAGATCCTGTCACAGAACTACAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA TCGCAGAGATCCTGTCACAGAACTACAGTGTT_GGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA CT C MIER2 Ensembl:ENSG00000105556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:334382..336172 26863196 MeRIP-seq:(Medium) rs1358482662 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4517652,Human_RBP_ID_18995527 Human_Splice_Rec_1928138,Human_Splice_Rec_1928139,Human_Splice_Rec_1928168,Human_Splice_Rec_1928169,Human_Splice_Rec_1928178,Human_Splice_Rec_1928179,Human_Splice_Rec_1928184,Human_Splice_Rec_1928185,Human_Splice_Rec_1928192,Human_Splice_Rec_1928193,Human_Splice_Rec_1928198 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850,RMVar_hsa_circ_190851,RMVar_hsa_circ_270394 79940 RMVar_ID_79940 Human_SNP_ID_654983697 m1A Human chr19 - 334474 334474 334474 TCGCAGAGATCCTGTCACAGAACTACAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA TCGCAGAGATCCTGTCACAGAACTACAGTGTTCGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA T G MIER2 Ensembl:ENSG00000105556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:334382..336172 26863196 MeRIP-seq:(Medium) rs11084956 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4517652,Human_RBP_ID_18995527 Human_Splice_Rec_1928138,Human_Splice_Rec_1928139,Human_Splice_Rec_1928168,Human_Splice_Rec_1928169,Human_Splice_Rec_1928178,Human_Splice_Rec_1928179,Human_Splice_Rec_1928184,Human_Splice_Rec_1928185,Human_Splice_Rec_1928192,Human_Splice_Rec_1928193,Human_Splice_Rec_1928198 GWAS_ID_9595,GWAS_ID_9596,GWAS_ID_9597 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850,RMVar_hsa_circ_190851,RMVar_hsa_circ_270394 79941 RMVar_ID_79941 Human_SNP_ID_654983702 m1A Human chr19 - 334482 334482 334482 GTTCAACCTCGCAGAGATCCTGTCACAGAACTACAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGA GTTCAACCTCGCAGAGATCCTGTCACAGAACTGCAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGA T C MIER2 Ensembl:ENSG00000105556 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:334432..340541 32194978 MeRIP-seq:(Medium) rs1396505587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4517653,Human_RBP_ID_18995527 Human_Splice_Rec_1928138,Human_Splice_Rec_1928139,Human_Splice_Rec_1928168,Human_Splice_Rec_1928169,Human_Splice_Rec_1928178,Human_Splice_Rec_1928179,Human_Splice_Rec_1928184,Human_Splice_Rec_1928185,Human_Splice_Rec_1928192,Human_Splice_Rec_1928193,Human_Splice_Rec_1928198 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850,RMVar_hsa_circ_190851,RMVar_hsa_circ_270394 79942 RMVar_ID_79942 Human_SNP_ID_654986833 m1A Human chr19 - 344320 344320 344320 GTGCTGGGGCCGCCAGGCGCCCCGCGCTCCCCATCGGGATCCCGGTGGACCCACCGCGCCTCCGC GTGCTGGGGCCGCCAGGCGCCCCGCGCTCCCCGTCGGGATCCCGGTGGACCCACCGCGCCTCCGC T C MIER2 Ensembl:ENSG00000105556 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:344286..344419 26863196 MeRIP-seq:(Medium) rs1486952634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9327896,Human_RBP_ID_18460812,Human_RBP_ID_24419113 RMVar_hsa_circ_104451,RMVar_hsa_circ_190836,RMVar_hsa_circ_120898,RMVar_hsa_circ_81506,RMVar_hsa_circ_190843,RMVar_hsa_circ_190848 79943 RMVar_ID_79943 Human_SNP_ID_655011433 m1A Human chr19 + 409249 409249 409249 CGCGCCCGCGCCCGCGCCCCCGCCCCCGCGGGAAGGGGGTGGGGCCGTCTCCCCGCAGCCCCCGG CGCGCCCGCGCCCGCGCCCCCGCCCCCGCGGGTAGGGGGTGGGGCCGTCTCCCCGCAGCCCCCGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:409226..409275 26863196 MeRIP-seq:(Medium) rs1382079311 Functional Loss SNV dbSNP153 33..33 33 - - - 79944 RMVar_ID_79944 Human_SNP_ID_655020836 m1A Human chr19 + 434716 434715 434716 CATCCCCCCGAGGGCAGAGGCTGACCTGGTCGAGGGCCGTGAGGGCGCAGGGCTGTGTCAGGGCC CATCCCCCCGAGGGCAGAGGCTGACCTGGTCG_GGGCCGTGAGGGCGCAGGGCTGTGTCAGGGCC GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:422787..434767 32194978 MeRIP-seq:(Medium) rs751662423 Functional Loss DEL dbSNP153 33..33 33 - - - 79945 RMVar_ID_79945 Human_SNP_ID_655023087 m1A Human chr19 + 440910 440910 440910 GCGTGTTAAAGTCCAGGGAGCGCATAGAGCGGAGAACCTCGATGCAGCCCATGTACTGAGGGGAG GCGTGTTAAAGTCCAGGGAGCGCATAGAGCGGGGAACCTCGATGCAGCCCATGTACTGAGGGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:439482..460598 32194978 MeRIP-seq:(Medium) rs1325722163 Functional Loss SNV dbSNP153 33..33 33 - - - 79946 RMVar_ID_79946 Human_SNP_ID_655030299 m1A Human chr19 + 460678 460660 460678 CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCGACCCCCGCGACCCCGCGCCCCGACAGCGGCTGA CCCGGACCCCGCCGC__________________CCCCCGCGACCCCGCGCCCCGACAGCGGCTGA CCCCCCGCCCGCCCCGCGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:460590..460699 26863410 MeRIP-seq:(Medium) rs939178892 Functional Loss DEL dbSNP153 16..33 33 - - - 79947 RMVar_ID_79947 Human_SNP_ID_655030314 m1A Human chr19 + 460678 460670 460679 CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCGACCCCCGCGACCCCGCGCCCCGACAGCGGCTGA CCCGGACCCCGCCGCCCCCCGCCCG_________CCCCGCGACCCCGCGCCCCGACAGCGGCTGA GCCCCGCGAC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:460590..460699 26863410 MeRIP-seq:(Medium) rs1056728787 Functional Loss DEL dbSNP153 26..34 33 - - - 79948 RMVar_ID_79948 Human_SNP_ID_655030319 m1A Human chr19 + 460678 460677 460679 CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCGACCCCCGCGACCCCGCGCCCCGACAGCGGCTGA CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCG__CCCCGCGACCCCGCGCCCCGACAGCGGCTGA GAC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:460590..460699 26863410 MeRIP-seq:(Medium) rs1322779573 Functional Loss DEL dbSNP153 33..34 33 - - - 79949 RMVar_ID_79949 Human_SNP_ID_655030320 m1A Human chr19 + 460678 460678 460678 CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCGACCCCCGCGACCCCGCGCCCCGACAGCGGCTGA CCCGGACCCCGCCGCCCCCCGCCCGCCCCGCGCCCCCCGCGACCCCGCGCCCCGACAGCGGCTGA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:460590..460699 26863410 MeRIP-seq:(Medium) rs1047827257 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 79950 RMVar_ID_79950 Human_SNP_ID_655040505 m1A Human chr19 + 489207 489194 489207 CACCCGCGGAAAAGGAGGGGGAGCGGCTGGTCAGCTGCGCCCTGCGGGTCGAGAATGTCATCAGC CACCCGCGGAAAAGGAGGGG_____________GCTGCGCCCTGCGGGTCGAGAATGTCATCAGC GGAGCGGCTGGTCA G MADCAM1 Ensembl:ENSG00000099866 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:489204..489354 26863196 MeRIP-seq:(Medium) rs954256281 Functional Loss DEL dbSNP153 21..33 33 - - - 79951 RMVar_ID_79951 Human_SNP_ID_655040561 m1A Human chr19 - 489324 489322 489324 GTCGGGGCCGCGGGCTGCGACGGCGGGTCGGGAGTCGGGGCTCGGCCTGCGAGGGTGGGTCAAGG GTCGGGGCCGCGGGCTGCGACGGCGGGTCGGG__TCGGGGCTCGGCCTGCGAGGGTGGGTCAAGG ACT A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:489273..489569 26863410 MeRIP-seq:(Medium) rs1427574184 Functional Loss DEL dbSNP153 33..34 33 - - - 79952 RMVar_ID_79952 Human_SNP_ID_655040562 m1A Human chr19 - 489324 489324 489324 GTCGGGGCCGCGGGCTGCGACGGCGGGTCGGGAGTCGGGGCTCGGCCTGCGAGGGTGGGTCAAGG GTCGGGGCCGCGGGCTGCGACGGCGGGTCGGGGGTCGGGGCTCGGCCTGCGAGGGTGGGTCAAGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:489273..489569 26863410 MeRIP-seq:(Medium) rs1167791365 Functional Loss SNV dbSNP153 33..33 33 - - - 79953 RMVar_ID_79953 Human_SNP_ID_655042405 m1A Human chr19 + 494655 494655 494655 AGCCCCTCCTCTAGGCCTCAGTTTCCCTCCTCAGCACCCAGCCCCTCCCCCGAGCCTCATTTTGC AGCCCCTCCTCTAGGCCTCAGTTTCCCTCCTCTGCACCCAGCCCCTCCCCCGAGCCTCATTTTGC A T MADCAM1 Ensembl:ENSG00000099866 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:494652..494945 26863196 MeRIP-seq:(Medium) rs1295549505 Functional Loss SNV dbSNP153 33..33 33 - - - 79954 RMVar_ID_79954 Human_SNP_ID_655043267 m1A Human chr19 + 496944 496944 496944 GGGCGCGGGAGAGGGGAGGGGGCTCGGGGGAGAGGAAGGGGCGCGGTGAGCGGGGAGGGGACGCG GGGCGCGGGAGAGGGGAGGGGGCTCGGGGGAGGGGAAGGGGCGCGGTGAGCGGGGAGGGGACGCG A G MADCAM1 Ensembl:ENSG00000099866 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:496939..497057 26863196 MeRIP-seq:(Medium) rs1489002452 Functional Loss SNV dbSNP153 33..33 33 - - - 79955 RMVar_ID_79955 Human_SNP_ID_655043813 m1A Human chr19 + 498282 498282 498282 CCCCGGCCTTCGCTTCCCTCCAACTCACCCCAACTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT CCCCGGCCTTCGCTTCCCTCCAACTCACCCCACCTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT A C MADCAM1 Ensembl:ENSG00000099866 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:498277..498574 26863196 MeRIP-seq:(Medium) rs1267272580 Functional Loss SNV dbSNP153 33..33 33 - - - 79956 RMVar_ID_79956 Human_SNP_ID_655043814 m1A Human chr19 + 498282 498282 498282 CCCCGGCCTTCGCTTCCCTCCAACTCACCCCAACTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT CCCCGGCCTTCGCTTCCCTCCAACTCACCCCAGCTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT A G MADCAM1 Ensembl:ENSG00000099866 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:498277..498574 26863196 MeRIP-seq:(Medium) rs1267272580 Functional Loss SNV dbSNP153 33..33 33 - - - 79957 RMVar_ID_79957 Human_SNP_ID_655043815 m1A Human chr19 + 498282 498282 498282 CCCCGGCCTTCGCTTCCCTCCAACTCACCCCAACTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT CCCCGGCCTTCGCTTCCCTCCAACTCACCCCATCTCTCCCAGGGCCGGCCCTGGCCCATCCTCCT A T MADCAM1 Ensembl:ENSG00000099866 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:498277..498574 26863196 MeRIP-seq:(Medium) rs1267272580 Functional Loss SNV dbSNP153 33..33 33 - - - 79958 RMVar_ID_79958 Human_SNP_ID_655047289 m1A Human chr19 + 507533 507533 507533 GCGAAGATGGCGGCAGTGGAGAAGCGGCGGCAAGCGGTACCACCGCCGGCCGGTTTCACGGACAG GCGAAGATGGCGGCAGTGGAGAAGCGGCGGCATGCGGTACCACCGCCGGCCGGTTTCACGGACAG A T TPGS1 Ensembl:ENSG00000141933 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:507482..507663;chr19:507530..507751 26863196 MeRIP-seq:(Medium) rs781635771 Functional Loss SNV dbSNP153 33..33 33 - - - 79959 RMVar_ID_79959 Human_SNP_ID_655047686 m1A Human chr19 - 508487 508487 508487 CAACCACCTTCCCTGGGCTCAGAACTGGCCCCAGCCAGGGGACACCGCGCGTAGGCACCTGCAGC CAACCACCTTCCCTGGGCTCAGAACTGGCCCCTGCCAGGGGACACCGCGCGTAGGCACCTGCAGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:508482..508614 26863196 MeRIP-seq:(Medium) rs938976483 Functional Loss SNV dbSNP153 33..33 33 - - - 79960 RMVar_ID_79960 Human_SNP_ID_655050905 m1A Human chr19 - 517747 517747 517747 CCGCCTCCACCCAGCCTGGCCTCCCCCGTCCCAGCCCCTACCCAGCCTCGGCCTCCTCCTCCCAG CCGCCTCCACCCAGCCTGGCCTCCCCCGTCCCCGCCCCTACCCAGCCTCGGCCTCCTCCTCCCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:517745..518149 26863196 MeRIP-seq:(Medium) rs1479240302 Functional Loss SNV dbSNP153 33..33 33 - - - 79961 RMVar_ID_79961 Human_SNP_ID_655050920 m1A Human chr19 - 517783 517783 517783 TCGGCCTCCTCCTCCCAACCTGGGTCTCCCTCATCCCCGCCTCCACCCAGCCTGGCCTCCCCCGT TCGGCCTCCTCCTCCCAACCTGGGTCTCCCTCCTCCCCGCCTCCACCCAGCCTGGCCTCCCCCGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:517774..518165 26863196 MeRIP-seq:(Medium) rs1297890627 Functional Loss SNV dbSNP153 33..33 33 - - - 79962 RMVar_ID_79962 Human_SNP_ID_655051404 m1A Human chr19 + 518871 518871 518871 CTGGGTGGGCGCGCGGTCTCTGCCGGCCCCCAACGTCCCCGTCTCCGCAGGGCCGCCTTCAACAA CTGGGTGGGCGCGCGGTCTCTGCCGGCCCCCACCGTCCCCGTCTCCGCAGGGCCGCCTTCAACAA A C TPGS1 Ensembl:ENSG00000141933 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:518870..519250 26863196 MeRIP-seq:(Medium) rs767130189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581776,Human_RBP_ID_8194774,Human_RBP_ID_9425499 79963 RMVar_ID_79963 Human_SNP_ID_655054294 m1A Human chr19 - 525051 525008 525052 GGGTCCAGGTGGGAGAGGGTGTTGGCTGGACCAGCCGGGGGCGGTGAAGGGCTGGGGGTCCAGGT GGGTCCAGGTGGGAGAGGGTGTTGGCTGGAC__________________________________ CACCCTCTCCCACCTGGACCCCCAGCCCTTCACCGCCCCCGGCTG C lnc-ODF3L2-3 RNACentral:URS00008C19A1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:525043..525173 26863196 MeRIP-seq:(Medium) rs1312736316 Functional Loss DEL dbSNP153 32..65 33 - - - 79964 RMVar_ID_79964 Human_SNP_ID_655054314 m1A Human chr19 - 525051 525049 525051 GGGTCCAGGTGGGAGAGGGTGTTGGCTGGACCAGCCGGGGGCGGTGAAGGGCTGGGGGTCCAGGT GGGTCCAGGTGGGAGAGGGTGTTGGCTGGACC__CCGGGGGCGGTGAAGGGCTGGGGGTCCAGGT GCT G lnc-ODF3L2-3 RNACentral:URS00008C19A1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:525043..525173 26863196 MeRIP-seq:(Medium) rs1194666975 Functional Loss DEL dbSNP153 33..34 33 - - - 79965 RMVar_ID_79965 Human_SNP_ID_655056621 m1A Human chr19 + 531817 531790 531817 CCGGGCGGCGGCGGCGGCGCAGAGGAGGAGGCAGGCGGCGGCCCCGGTGGCTCCCCCCCGGACGG CCGGGC___________________________GGCGGCGGCCCCGGTGGCTCCCCCCCGGACGG CGGCGGCGGCGGCGCAGAGGAGGAGGCA C CDC34 Ensembl:ENSG00000099804 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:531721..531911 26863410 MeRIP-seq:(Medium) rs1005538941 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_4556909,Human_RBP_ID_5320626,Human_RBP_ID_9327903,Human_RBP_ID_22447057,Human_RBP_ID_27562773 RMVar_hsa_circ_76840,RMVar_hsa_circ_190858 79966 RMVar_ID_79966 Human_SNP_ID_655056642 m1A Human chr19 - 531832 531832 531832 GGGCCGGGCCGCGCACCGTCCGGGGGGGAGCCACCGGGGCCGCCGCCTGCCTCCTCCTCTGCGCC GGGCCGGGCCGCGCACCGTCCGGGGGGGAGCCGCCGGGGCCGCCGCCTGCCTCCTCCTCTGCGCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:531733..531961 26863410 MeRIP-seq:(Medium) rs1313778360 Functional Loss SNV dbSNP153 33..33 33 - - - 79967 RMVar_ID_79967 Human_SNP_ID_655056724 m1A Human chr19 - 532020 532018 532020 AGTTGTATAGATCGCCCTCGTCCACCAGTGTCACGCGGAATCCCTCGACCGGCTCTTCCTGCAGC AGTTGTATAGATCGCCCTCGTCCACCAGTGTC__GCGGAATCCCTCGACCGGCTCTTCCTGCAGC CGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:531726..532139 26863196 MeRIP-seq:(Medium) rs1362360888 Functional Loss DEL dbSNP153 33..34 33 - - - 79968 RMVar_ID_79968 Human_SNP_ID_655058851 m1A Human chr19 - 537144 537144 537144 CCTCCCGTGACGCCCCCGCCCGCCCTCACCGGATGATGTCTGTGTACTCCCGATCCTTCCCCTTG CCTCCCGTGACGCCCCCGCCCGCCCTCACCGGGTGATGTCTGTGTACTCCCGATCCTTCCCCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:537022..542025 26863196 MeRIP-seq:(Medium) rs763970240 Functional Loss SNV dbSNP153 33..33 33 - - - 79969 RMVar_ID_79969 Human_SNP_ID_655059553 m1A Human chr19 - 538876 538842 538877 CCGGGGCCACCGAGGACATCTGCACCAGAGGGACGGCCAGGGCAGCTACCCTGTGACCTCCAGAG CCGGGGCCACCGAGGACATCTGCACCAGAGG__________________________________ GCCTCTGGAGGTCACAGGGTAGCTGCCCTGGCCGTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:538870..538996 26863196 MeRIP-seq:(Medium) rs1204265875 Functional Loss DEL dbSNP153 32..65 33 - - - 79970 RMVar_ID_79970 Human_SNP_ID_655059559 m1A Human chr19 - 538865 538865 538865 GAGGACATCTGCACCAGAGGGACGGCCAGGGCAGCTACCCTGTGACCTCCAGAGGCCAGCAGGTG GAGGACATCTGCACCAGAGGGACGGCCAGGGCGGCTACCCTGTGACCTCCAGAGGCCAGCAGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:538862..538999 26863196 MeRIP-seq:(Medium) rs990153804 Functional Loss SNV dbSNP153 33..33 33 - - - 79971 RMVar_ID_79971 Human_SNP_ID_655059567 m1A Human chr19 + 538890 538890 538890 GGGTAGCTGCCCTGGCCGTCCCTCTGGTGCAGATGTCCTCGGTGGCCCCGGTCCGGTCGTGTCAC GGGTAGCTGCCCTGGCCGTCCCTCTGGTGCAGTTGTCCTCGGTGGCCCCGGTCCGGTCGTGTCAC A T CDC34 Ensembl:ENSG00000099804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:538887..538973 26863196 MeRIP-seq:(Medium) rs1462842571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13505321 RMVar_hsa_circ_76840,RMVar_hsa_circ_78258,RMVar_hsa_circ_190858,RMVar_hsa_circ_101167,RMVar_hsa_circ_190859,RMVar_hsa_circ_190860 79972 RMVar_ID_79972 Human_SNP_ID_655060681 m1A Human chr19 + 541464 541464 541464 GGCGCCCGACGAGGGCTCAGACCTCTTCTACGACGACTACTACGAGGACGGCGAGGTGGAGGAGG GGCGCCCGACGAGGGCTCAGACCTCTTCTACGGCGACTACTACGAGGACGGCGAGGTGGAGGAGG A G CDC34 Ensembl:ENSG00000099804 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:541413..541987 26863196 MeRIP-seq:(Medium) rs1161096646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8493324,Human_RBP_ID_18441925,Human_RBP_ID_22975771,Human_RBP_ID_27278009 RMVar_hsa_circ_76840,RMVar_hsa_circ_78258,RMVar_hsa_circ_190858,RMVar_hsa_circ_101167,RMVar_hsa_circ_190859,RMVar_hsa_circ_190860 79973 RMVar_ID_79973 Human_SNP_ID_655064567 m1A Human chr19 - 550625 550625 550625 ACTGTTTTCAGGGTGCTGGGGTGACAGGGGACAGGCCTGTTTTCGGGGTGCTGGGGTGACTGGGG ACTGTTTTCAGGGTGCTGGGGTGACAGGGGACGGGCCTGTTTTCGGGGTGCTGGGGTGACTGGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:550623..550807 26863196 MeRIP-seq:(Medium) rs28405852 Functional Loss SNV dbSNP153 33..33 33 - - - 79974 RMVar_ID_79974 Human_SNP_ID_655067948 m1A Human chr19 - 559289 559289 559289 AACCCCATCCAGGGCGAAGGCTGGGCCCAGCCAGGGTGGGAAGATGCTGGGGGCCGAGGGCCTGG AACCCCATCCAGGGCGAAGGCTGGGCCCAGCCGGGGTGGGAAGATGCTGGGGGCCGAGGGCCTGG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:559208..559337 26863196 MeRIP-seq:(Medium) rs1376127629 Functional Loss SNV dbSNP153 33..33 33 - - - 79975 RMVar_ID_79975 Human_SNP_ID_655069114 m1A Human chr19 + 562060 562059 562061 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCGGGATTGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACC__GTTAGCCGGGATTGTCTCGATCTCCTGACCT CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:562052..562231 26863196 MeRIP-seq:(Medium) rs1394624405 Functional Loss DEL dbSNP153 33..34 33 - - - 79976 RMVar_ID_79976 Human_SNP_ID_655069115 m1A Human chr19 + 562060 562060 562060 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCGGGATTGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCGGGATTGTCTCGATCTCCTGACCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:562052..562231 26863196 MeRIP-seq:(Medium) rs62132589 Functional Loss SNV dbSNP153 33..33 33 - - - 79977 RMVar_ID_79977 Human_SNP_ID_655070818 m1A Human chr19 + 566651 566651 566651 TGGCAGAGTATTTTACGGGGAGCGGGAAACGGAAGGAGGAGTCTGGTTCTTATCTTTGCACGGGG TGGCAGAGTATTTTACGGGGAGCGGGAAACGGGAGGAGGAGTCTGGTTCTTATCTTTGCACGGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:566641..566724 26863196 MeRIP-seq:(Medium) rs1263268640 Functional Loss SNV dbSNP153 33..33 33 - - - 79978 RMVar_ID_79978 Human_SNP_ID_655072710 m1A Human chr19 + 571241 571241 571241 GTCCTGATCTGCAGAGATGGCACCTGCCACCCACTCTGCACATCCCCCTCCCGTCGCCACGGGCT GTCCTGATCTGCAGAGATGGCACCTGCCACCCCCTCTGCACATCCCCCTCCCGTCGCCACGGGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:571237..571556 26863196 MeRIP-seq:(Medium) rs1174215611 Functional Loss SNV dbSNP153 33..33 33 - - - 79979 RMVar_ID_79979 Human_SNP_ID_655073353 m1A Human chr19 + 572628 572628 572628 AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATGGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT A G BSG Ensembl:ENSG00000172270 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:572601..572814 26863196 MeRIP-seq:(Medium) rs12609610 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_527547,Human_RBP_ID_1572151,Human_RBP_ID_4549119,Human_RBP_ID_5319662,Human_RBP_ID_5500220,Human_RBP_ID_6786275,Human_RBP_ID_8494652,Human_RBP_ID_9327907,Human_RBP_ID_13516791,Human_RBP_ID_18191511,Human_RBP_ID_22069333,Human_RBP_ID_22446237,Human_RBP_ID_25435042,Human_RBP_ID_26470397,Human_RBP_ID_26769705,Human_RBP_ID_26995957,Human_RBP_ID_27471685 Human_Splice_Rec_1928489,Human_Splice_Rec_1928491,Human_Splice_Rec_1928499,Human_Splice_Rec_1928513,Human_Splice_Rec_1928517,Human_Splice_Rec_1928519,Human_Splice_Rec_1928529,Human_Splice_Rec_1928545,Human_Splice_Rec_1928553,Human_Splice_Rec_1928563 GWAS_ID_9598,GWAS_ID_9599 RMVar_hsa_circ_111780,RMVar_hsa_circ_190861 79980 RMVar_ID_79980 Human_SNP_ID_655073354 m1A Human chr19 + 572628 572628 572628 AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATTGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT A T BSG Ensembl:ENSG00000172270 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:572601..572814 26863196 MeRIP-seq:(Medium) rs12609610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527547,Human_RBP_ID_1572151,Human_RBP_ID_4549119,Human_RBP_ID_5319662,Human_RBP_ID_5500220,Human_RBP_ID_6786275,Human_RBP_ID_8494652,Human_RBP_ID_9327907,Human_RBP_ID_13516791,Human_RBP_ID_18191511,Human_RBP_ID_22069333,Human_RBP_ID_22446237,Human_RBP_ID_25435042,Human_RBP_ID_26470397,Human_RBP_ID_26769705,Human_RBP_ID_26995957,Human_RBP_ID_27471685 Human_Splice_Rec_1928489,Human_Splice_Rec_1928491,Human_Splice_Rec_1928499,Human_Splice_Rec_1928513,Human_Splice_Rec_1928517,Human_Splice_Rec_1928519,Human_Splice_Rec_1928529,Human_Splice_Rec_1928545,Human_Splice_Rec_1928553,Human_Splice_Rec_1928563 GWAS_ID_9598,GWAS_ID_9599 RMVar_hsa_circ_111780,RMVar_hsa_circ_190861 79981 RMVar_ID_79981 Human_SNP_ID_655073365 m1A Human chr19 + 572635 572635 572635 GGAGGTTGTAGGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCTGGGATTC GGAGGTTGTAGGACCGGCGAGGAATAGGAATCGTGGCGGCTGCGCTGTTCGTGCTGCTGGGATTC A G BSG Ensembl:ENSG00000172270 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:572601..572782 26863196 MeRIP-seq:(Medium) rs374628867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527547,Human_RBP_ID_1572151,Human_RBP_ID_4549119,Human_RBP_ID_5319662,Human_RBP_ID_5500220,Human_RBP_ID_6786275,Human_RBP_ID_8494652,Human_RBP_ID_9327907,Human_RBP_ID_13516792,Human_RBP_ID_18191511,Human_RBP_ID_22069333,Human_RBP_ID_22446237,Human_RBP_ID_25435042,Human_RBP_ID_26470397,Human_RBP_ID_26769705,Human_RBP_ID_26995957,Human_RBP_ID_27471685 Human_Splice_Rec_1928489,Human_Splice_Rec_1928491,Human_Splice_Rec_1928499,Human_Splice_Rec_1928513,Human_Splice_Rec_1928517,Human_Splice_Rec_1928519,Human_Splice_Rec_1928529,Human_Splice_Rec_1928545,Human_Splice_Rec_1928553,Human_Splice_Rec_1928563 RMVar_hsa_circ_111780,RMVar_hsa_circ_190861 79982 RMVar_ID_79982 Human_SNP_ID_655073372 m1A Human chr19 - 572643 572643 572643 AGCAGCGCGAATCCCAGCAGCACGAACAGCGCAGCCGCCATGATTCCTATTCCTCGCCGGTCCTA AGCAGCGCGAATCCCAGCAGCACGAACAGCGCTGCCGCCATGATTCCTATTCCTCGCCGGTCCTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:572576..575055 26863196 MeRIP-seq:(Medium) rs924673090 Functional Loss SNV dbSNP153 33..33 33 - - - 79983 RMVar_ID_79983 Human_SNP_ID_655073373 m1A Human chr19 - 572643 572643 572643 AGCAGCGCGAATCCCAGCAGCACGAACAGCGCAGCCGCCATGATTCCTATTCCTCGCCGGTCCTA AGCAGCGCGAATCCCAGCAGCACGAACAGCGCGGCCGCCATGATTCCTATTCCTCGCCGGTCCTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:572576..575055 26863196 MeRIP-seq:(Medium) rs924673090 Functional Loss SNV dbSNP153 33..33 33 - - - 79984 RMVar_ID_79984 Human_SNP_ID_655073379 m1A Human chr19 - 572648 572648 572648 TGCCCAGCAGCGCGAATCCCAGCAGCACGAACAGCGCAGCCGCCATGATTCCTATTCCTCGCCGG TGCCCAGCAGCGCGAATCCCAGCAGCACGAACTGCGCAGCCGCCATGATTCCTATTCCTCGCCGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:572576..573117 26863196 MeRIP-seq:(Medium) rs914485079 Functional Loss SNV dbSNP153 33..33 33 - - - 79985 RMVar_ID_79985 Human_SNP_ID_655073380 m1A Human chr19 - 572648 572648 572648 TGCCCAGCAGCGCGAATCCCAGCAGCACGAACAGCGCAGCCGCCATGATTCCTATTCCTCGCCGG TGCCCAGCAGCGCGAATCCCAGCAGCACGAACGGCGCAGCCGCCATGATTCCTATTCCTCGCCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:572576..573117 26863196 MeRIP-seq:(Medium) rs914485079 Functional Loss SNV dbSNP153 33..33 33 - - - 79986 RMVar_ID_79986 Human_SNP_ID_655073382 m1A Human chr19 - 572650 572650 572650 GGTGCCCAGCAGCGCGAATCCCAGCAGCACGAACAGCGCAGCCGCCATGATTCCTATTCCTCGCC GGTGCCCAGCAGCGCGAATCCCAGCAGCACGAGCAGCGCAGCCGCCATGATTCCTATTCCTCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:572576..572820 26863196 MeRIP-seq:(Medium) rs760728600 Functional Loss SNV dbSNP153 33..33 33 - - - 79987 RMVar_ID_79987 Human_SNP_ID_655076295 m1A Human chr19 + 579424 579424 579424 ATGAAAACCAGTCCTTCCCGGGGAGGAGCCGCAGGTTCCTGGGGGTCAGGCAGGCAGCGCGGGCC ATGAAAACCAGTCCTTCCCGGGGAGGAGCCGCGGGTTCCTGGGGGTCAGGCAGGCAGCGCGGGCC A G BSG Ensembl:ENSG00000172270 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:579422..579600 26863196 MeRIP-seq:(Medium) rs763650312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3579661,Human_RBP_ID_8098877,Human_RBP_ID_18165211,Human_RBP_ID_18488385,Human_RBP_ID_22416504 RMVar_hsa_circ_111780,RMVar_hsa_circ_120957,RMVar_hsa_circ_190861,RMVar_hsa_circ_190862 79988 RMVar_ID_79988 Human_SNP_ID_655076319 m1A Human chr19 - 579458 579458 579458 CCGGCGAGACGCGGTCAGCAGAGTGGAGGAGCACGGCCCGCGCTGCCTGCCTGACCCCCAGGAAC CCGGCGAGACGCGGTCAGCAGAGTGGAGGAGCGCGGCCCGCGCTGCCTGCCTGACCCCCAGGAAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:579448..579700 26863410 MeRIP-seq:(Medium) rs201705588 Functional Loss SNV dbSNP153 33..33 33 - - - 79989 RMVar_ID_79989 Human_SNP_ID_655076445 m1A Human chr19 + 579643 579643 579643 TGGTGCTGAAGGAGGACGCGCTGCCCGGCCAGAAAACGGAGTTCAAGTGAGTGCCTGACCACGCC TGGTGCTGAAGGAGGACGCGCTGCCCGGCCAGGAAACGGAGTTCAAGTGAGTGCCTGACCACGCC A G BSG Ensembl:ENSG00000172270 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:579476..579675 32194978 MeRIP-seq:(Medium) rs1309058607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528027,Human_RBP_ID_913662,Human_RBP_ID_22446240,Human_RBP_ID_22762627 Human_Splice_Rec_1928465,Human_Splice_Rec_1928493,Human_Splice_Rec_1928501,Human_Splice_Rec_1928515,Human_Splice_Rec_1928521,Human_Splice_Rec_1928533,Human_Splice_Rec_1928547,Human_Splice_Rec_1928571,Human_Splice_Rec_1928583,Human_Splice_Rec_1928587 RMVar_hsa_circ_10111,RMVar_hsa_circ_111780,RMVar_hsa_circ_120957,RMVar_hsa_circ_190861,RMVar_hsa_circ_190862,RMVar_hsa_circ_373981,RMVar_hsa_circ_190863 79990 RMVar_ID_79990 Human_SNP_ID_655076885 m1A Human chr19 + 580705 580705 580705 CGTCAGAACACATCAACGAGGGGGAGACGGCCATGCTGGTCTGCAAGTCAGAGTCCGTGCCACCT CGTCAGAACACATCAACGAGGGGGAGACGGCCTTGCTGGTCTGCAAGTCAGAGTCCGTGCCACCT A T BSG Ensembl:ENSG00000172270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:580608..580816 26863196 MeRIP-seq:(Medium) rs769337628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54537,Human_RBP_ID_240640,Human_RBP_ID_528087,Human_RBP_ID_913665,Human_RBP_ID_4550318,Human_RBP_ID_18192564,Human_RBP_ID_18470337,Human_RBP_ID_22446243,Human_RBP_ID_22762634,Human_RBP_ID_22812634,Human_RBP_ID_26470521,Human_RBP_ID_26996219,Human_RBP_ID_27471884 Human_Splice_Rec_1928468,Human_Splice_Rec_1928469,Human_Splice_Rec_1928480,Human_Splice_Rec_1928481,Human_Splice_Rec_1928496,Human_Splice_Rec_1928497,Human_Splice_Rec_1928504,Human_Splice_Rec_1928505,Human_Splice_Rec_1928536,Human_Splice_Rec_1928537,Human_Splice_Rec_1928550,Human_Splice_Rec_1928551,Human_Splice_Rec_1928554,Human_Splice_Rec_1928555,Human_Splice_Rec_1928574,Human_Splice_Rec_1928575,Human_Splice_Rec_1928586,Human_Splice_Rec_1928590,Human_Splice_Rec_1928591 Human_miRNA_ID_2442303,Human_miRNA_ID_2442304 RMVar_hsa_circ_10111,RMVar_hsa_circ_111780,RMVar_hsa_circ_120957,RMVar_hsa_circ_190861,RMVar_hsa_circ_190862,RMVar_hsa_circ_373981,RMVar_hsa_circ_190864,RMVar_hsa_circ_123784,RMVar_hsa_circ_190863 79991 RMVar_ID_79991 Human_SNP_ID_655077375 m1A Human chr19 - 581593 581593 581593 GCAGGGCATGTGGGCAGGAGGGCAGACGGCTCACCATCCAGGACGTCCTCGGGCTTCCGGCGCTT GCAGGGCATGTGGGCAGGAGGGCAGACGGCTCGCCATCCAGGACGTCCTCGGGCTTCCGGCGCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr19:581287..581644;chr19:581576..581600 26863196,32194978 MeRIP-seq:(Medium) rs1276305265 Functional Loss SNV dbSNP153 33..33 33 - - - 79992 RMVar_ID_79992 Human_SNP_ID_655077808 m1A Human chr19 - 582571 582571 582571 AGGAGCTCCCGCCCACCGCACCTGCCTCAGGAAGAGTTCCTCTGGCGGACGTTCTTGCCTTTGTC AGGAGCTCCCGCCCACCGCACCTGCCTCAGGAGGAGTTCCTCTGGCGGACGTTCTTGCCTTTGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:582478..582614 26863196 MeRIP-seq:(Medium) rs1235506037 Functional Loss SNV dbSNP153 33..33 33 - - - 79993 RMVar_ID_79993 Human_SNP_ID_655077920 m1A Human chr19 + 582775 582775 582775 TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCACGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCCCGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT A C BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528158,Human_RBP_ID_772100,Human_RBP_ID_825640,Human_RBP_ID_913671,Human_RBP_ID_4550772,Human_RBP_ID_8495199,Human_RBP_ID_17386490,Human_RBP_ID_17655277,Human_RBP_ID_18740724,Human_RBP_ID_22446254,Human_RBP_ID_22533230,Human_RBP_ID_22763533,Human_RBP_ID_26475210 Human_Splice_Rec_1928476,Human_Splice_Rec_1928488,Human_Splice_Rec_1928512,Human_Splice_Rec_1928528,Human_Splice_Rec_1928544,Human_Splice_Rec_1928562,Human_Splice_Rec_1928568,Human_Splice_Rec_1928598 GWAS_ID_9600,GWAS_ID_9601 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 79994 RMVar_ID_79994 Human_SNP_ID_655077921 m1A Human chr19 + 582775 582775 582775 TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCACGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCGCGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT A G BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528158,Human_RBP_ID_772100,Human_RBP_ID_825640,Human_RBP_ID_913671,Human_RBP_ID_4550772,Human_RBP_ID_8495199,Human_RBP_ID_17386490,Human_RBP_ID_17655277,Human_RBP_ID_18740724,Human_RBP_ID_22446254,Human_RBP_ID_22533230,Human_RBP_ID_22763533,Human_RBP_ID_26475210 Human_Splice_Rec_1928476,Human_Splice_Rec_1928488,Human_Splice_Rec_1928512,Human_Splice_Rec_1928528,Human_Splice_Rec_1928544,Human_Splice_Rec_1928562,Human_Splice_Rec_1928568,Human_Splice_Rec_1928598 GWAS_ID_9600,GWAS_ID_9601 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 79995 RMVar_ID_79995 Human_SNP_ID_655078023 m1A Human chr19 - 582986 582985 582987 GCCATGACTCAGACCCAGAGGCTGAAAGCCACAGACGGGGCCGCAGGGCAGCAGCTCCCGGGCTC GCCATGACTCAGACCCAGAGGCTGAAAGCCA__GACGGGGCCGCAGGGCAGCAGCTCCCGGGCTC CTG C lnc-POLRMT-5 RNACentral:URS00008B2FCC lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:582959..583448 26863196 MeRIP-seq:(Medium) rs1369072582 Functional Loss DEL dbSNP153 32..33 33 - - - 79996 RMVar_ID_79996 Human_SNP_ID_655078167 m1A Human chr19 - 583414 583414 583414 GGGGTTCCCACGTGAGCCCTGGTGCTATAGAGAGCCGGCCGTCCTCCAGGGGTGAGCTGGGGAGG GGGGTTCCCACGTGAGCCCTGGTGCTATAGAGCGCCGGCCGTCCTCCAGGGGTGAGCTGGGGAGG T G lnc-POLRMT-5 RNACentral:URS00008B2FCC lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:583000..583447 26863410 MeRIP-seq:(Medium) rs1394840036 Functional Loss SNV dbSNP153 33..33 33 - - - 79997 RMVar_ID_79997 Human_SNP_ID_655078192 m1A Human chr19 + 583453 583453 583453 AGCACCAGGGCTCACGTGGGAACCCCCCTCCCACCCACCGCCACAATAAAGATCGCCCCCACCTC AGCACCAGGGCTCACGTGGGAACCCCCCTCCCCCCCACCGCCACAATAAAGATCGCCCCCACCTC A C BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA untreated chr19:583451..583500 31548705,26863196 m1A-quant-seq:(High) rs1380460423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528171,Human_RBP_ID_17502350,Human_RBP_ID_22976595 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 79998 RMVar_ID_79998 Human_SNP_ID_655078193 m1A Human chr19 + 583457 583457 583457 CCAGGGCTCACGTGGGAACCCCCCTCCCACCCACCGCCACAATAAAGATCGCCCCCACCTCCACC CCAGGGCTCACGTGGGAACCCCCCTCCCACCCCCCGCCACAATAAAGATCGCCCCCACCTCCACC A C BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1230109894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528171,Human_RBP_ID_22976595 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 79999 RMVar_ID_79999 Human_SNP_ID_655078194 m1A Human chr19 + 583457 583457 583457 CCAGGGCTCACGTGGGAACCCCCCTCCCACCCACCGCCACAATAAAGATCGCCCCCACCTCCACC CCAGGGCTCACGTGGGAACCCCCCTCCCACCCGCCGCCACAATAAAGATCGCCCCCACCTCCACC A G BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1230109894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528171,Human_RBP_ID_22976595 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 80000 RMVar_ID_80000 Human_SNP_ID_655080818 m1A Human chr19 + 590381 590381 590381 CGCCGGGGCCGGGGCCGGCGGAGGAGGCGGGCAGCGAGGAGGCGGGCCCGGCGGGGGAGCCGCGC CGCCGGGGCCGGGGCCGGCGGAGGAGGCGGGCGGCGAGGAGGCGGGCCCGGCGGGGGAGCCGCGC A G HCN2 Ensembl:ENSG00000099822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:589941..590456;chr19:590121..590466 26863196 MeRIP-seq:(Medium) rs552260789 Functional Loss SNV dbSNP153 33..33 33 - - - 80001 RMVar_ID_80001 Human_SNP_ID_655080878 m1A Human chr19 - 590537 590537 590537 GCTGTACGGGTGGATGATCCAGGCCCCCGCCGACTTGACGCGCTCCTGCTCGCGCTCCACGGCCT GCTGTACGGGTGGATGATCCAGGCCCCCGCCGGCTTGACGCGCTCCTGCTCGCGCTCCACGGCCT T C AC005559.1 Ensembl:ENSG00000267036 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:590188..603600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 80002 RMVar_ID_80002 Human_SNP_ID_655089003 m1A Human chr19 + 611323 611323 611323 GCGGGGCCTAGGGATGGCGGCCGTGATCACGCAGGCAGCAGAGAGCAGCTCTGGGAAGCGGGGAG GCGGGGCCTAGGGATGGCGGCCGTGATCACGCGGGCAGCAGAGAGCAGCTCTGGGAAGCGGGGAG A G HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:611312..611509 26863196 MeRIP-seq:(Medium) rs979078177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53125 80003 RMVar_ID_80003 Human_SNP_ID_655090874 m1A Human chr19 - 614069 614069 614069 ACTGTCCAAGCCACTCTCCTGATGCCTTGGCCACGCCCCTCCCCCGCCAGGGCACCCGCCCCGGC ACTGTCCAAGCCACTCTCCTGATGCCTTGGCCGCGCCCCTCCCCCGCCAGGGCACCCGCCCCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:614042..614190 26863196 MeRIP-seq:(Medium) rs1355140186 Functional Loss SNV dbSNP153 33..33 33 - - - 80004 RMVar_ID_80004 Human_SNP_ID_655090893 m1A Human chr19 + 614099 614099 614099 CGTGGCCAAGGCATCAGGAGAGTGGCTTGGACAGTGGCAGGGGGAAGGGCGTGGCTGTGGCATCA CGTGGCCAAGGCATCAGGAGAGTGGCTTGGACCGTGGCAGGGGGAAGGGCGTGGCTGTGGCATCA A C HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:614094..614217 26863196 MeRIP-seq:(Medium) rs1189643295 Functional Loss SNV dbSNP153 33..33 33 - - - 80005 RMVar_ID_80005 Human_SNP_ID_655090894 m1A Human chr19 + 614099 614099 614099 CGTGGCCAAGGCATCAGGAGAGTGGCTTGGACAGTGGCAGGGGGAAGGGCGTGGCTGTGGCATCA CGTGGCCAAGGCATCAGGAGAGTGGCTTGGACGGTGGCAGGGGGAAGGGCGTGGCTGTGGCATCA A G HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:614094..614217 26863196 MeRIP-seq:(Medium) rs1189643295 Functional Loss SNV dbSNP153 33..33 33 - - - 80006 RMVar_ID_80006 Human_SNP_ID_655091049 m1A Human chr19 + 614442 614442 614442 AGGCTTATGGACTGGTGATGAAATCACACACGACTGGGCTGTGTGCCAGCAGGGCAGGTGGGGCC AGGCTTATGGACTGGTGATGAAATCACACACGGCTGGGCTGTGTGCCAGCAGGGCAGGTGGGGCC A G HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:614437..614708 26863196 MeRIP-seq:(Medium) rs1340032361 Functional Loss SNV dbSNP153 33..33 33 - - - 80007 RMVar_ID_80007 Human_SNP_ID_655091137 m1A Human chr19 + 614645 614642 614645 GAGAGCCAGGGAGGCCTGGAGGAGGTTGGGGAAGAAGGGGAGGCCAGACACACAGGGCCCAGTGG GAGAGCCAGGGAGGCCTGGAGGAGGTTGGG___GAAGGGGAGGCCAGACACACAGGGCCCAGTGG GGAA G HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:614364..614962 26863196 MeRIP-seq:(Medium) rs1568369436 Functional Loss DEL dbSNP153 31..33 33 - - - 80008 RMVar_ID_80008 Human_SNP_ID_655091739 m1A Human chr19 + 615891 615891 615891 CCAGGAGAACGCCATCATCCAGGAGATCGTCAAGTACGACCGCGAGATGGTGCAGCAGGCCGAGC CCAGGAGAACGCCATCATCCAGGAGATCGTCAGGTACGACCGCGAGATGGTGCAGCAGGCCGAGC A G HCN2 Ensembl:ENSG00000099822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:615867..616024 26863196 MeRIP-seq:(Medium) rs1408213157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928612 80009 RMVar_ID_80009 Human_SNP_ID_655091966 m1A Human chr19 + 616188 616188 616188 CGCCAGCCCCCGGGCACCGCGGACCTCGCCCTACGGCGGCCTGCCCGCCGCCCCCCTTGCTGGGC CGCCAGCCCCCGGGCACCGCGGACCTCGCCCTTCGGCGGCCTGCCCGCCGCCCCCCTTGCTGGGC A T HCN2 Ensembl:ENSG00000099822 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr19:616176..617073;chr19:615973..616418 26863196,26863410 MeRIP-seq:(Medium) rs1449219480 Functional Loss SNV dbSNP153 33..33 33 - - - 80010 RMVar_ID_80010 Human_SNP_ID_655092128 m1A Human chr19 - 616406 616406 616406 CTGGGGGTCCAGGCCGCCGGCGGCGCCGGGTGAGGCCGAGTCCCTGCGGTCCGGGCTGGGCGCGG CTGGGGGTCCAGGCCGCCGGCGGCGCCGGGTGTGGCCGAGTCCCTGCGGTCCGGGCTGGGCGCGG T A lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:616319..616625 26863410 MeRIP-seq:(Medium) rs1178638097 Functional Loss SNV dbSNP153 33..33 33 - - - 80011 RMVar_ID_80011 Human_SNP_ID_655092129 m1A Human chr19 - 616406 616406 616406 CTGGGGGTCCAGGCCGCCGGCGGCGCCGGGTGAGGCCGAGTCCCTGCGGTCCGGGCTGGGCGCGG CTGGGGGTCCAGGCCGCCGGCGGCGCCGGGTGGGGCCGAGTCCCTGCGGTCCGGGCTGGGCGCGG T C lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:616319..616625 26863410 MeRIP-seq:(Medium) rs1178638097 Functional Loss SNV dbSNP153 33..33 33 - - - 80012 RMVar_ID_80012 Human_SNP_ID_655092190 m1A Human chr19 + 616484 616484 616484 CGCGCCTCTCGTCCAACTTGTGACCCTCGCCGACCGCCCCGCGGGCCCAGGCGGGCCGGGGGCGG CGCGCCTCTCGTCCAACTTGTGACCCTCGCCGGCCGCCCCGCGGGCCCAGGCGGGCCGGGGGCGG A G HCN2 Ensembl:ENSG00000099822 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:616470..616997 26863196 MeRIP-seq:(Medium) rs975195009 Functional Loss SNV dbSNP153 33..33 33 - - - 80013 RMVar_ID_80013 Human_SNP_ID_655092221 m1A Human chr19 - 616525 616525 616525 CGGGGCAGCGCAATGGCATGGCTTTGGTCTGGATGACGGCCCCGCCCCCGGCCCGCCTGGGCCCG CGGGGCAGCGCAATGGCATGGCTTTGGTCTGGGTGACGGCCCCGCCCCCGGCCCGCCTGGGCCCG T C lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:616209..616635 26863196 MeRIP-seq:(Medium) rs1203114273 Functional Loss SNV dbSNP153 33..33 33 - - - 80014 RMVar_ID_80014 Human_SNP_ID_655092261 m1A Human chr19 + 616587 616585 616587 CCGGCCGCCAGTCCGCCCAGAAGCCATAGACGAGACGTAGGTAGCCGTAGTTGGACGGACGGGCA CCGGCCGCCAGTCCGCCCAGAAGCCATAGAC__GACGTAGGTAGCCGTAGTTGGACGGACGGGCA CGA C HCN2 Ensembl:ENSG00000099822 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:616142..617150 26863196 MeRIP-seq:(Medium) rs1251410595 Functional Loss DEL dbSNP153 32..33 33 - - - 80015 RMVar_ID_80015 Human_SNP_ID_655092465 m1A Human chr19 - 616828 616828 616828 AAAACGATCCTCCTCGGACGGGGGCCACCTAGAGGGTGGGGGGCGGGCGGGGCTCCACAGCCGGC AAAACGATCCTCCTCGGACGGGGGCCACCTAGGGGGTGGGGGGCGGGCGGGGCTCCACAGCCGGC T C lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:616822..617150 26863196 MeRIP-seq:(Medium) rs1480419782 Functional Loss SNV dbSNP153 33..33 33 - - - 80016 RMVar_ID_80016 Human_SNP_ID_655092470 m1A Human chr19 - 616834 616834 616834 ACTTAGAAAACGATCCTCCTCGGACGGGGGCCACCTAGAGGGTGGGGGGCGGGCGGGGCTCCACA ACTTAGAAAACGATCCTCCTCGGACGGGGGCCGCCTAGAGGGTGGGGGGCGGGCGGGGCTCCACA T C lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:616828..617081 26863196 MeRIP-seq:(Medium) rs971643647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13530654 80017 RMVar_ID_80017 Human_SNP_ID_655092941 m1A Human chr19 - 617325 617325 617325 GCCACCCACGCCGTCCGCTCTGCTTCCTCCGCAGGGGCCTTCGACCTGGAGCAGGTGAAGCGTTC GCCACCCACGCCGTCCGCTCTGCTTCCTCCGCGGGGGCCTTCGACCTGGAGCAGGTGAAGCGTTC T C POLRMT Ensembl:ENSG00000099821 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:617226..617419 26863410 MeRIP-seq:(Medium) rs531160208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19088247 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_122408,RMVar_hsa_circ_125915,RMVar_hsa_circ_128093,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_105438,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190880,RMVar_hsa_circ_190882,RMVar_hsa_circ_190881,RMVar_hsa_circ_190879,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869 80018 RMVar_ID_80018 Human_SNP_ID_655092942 m1A Human chr19 - 617325 617325 617325 GCCACCCACGCCGTCCGCTCTGCTTCCTCCGCAGGGGCCTTCGACCTGGAGCAGGTGAAGCGTTC GCCACCCACGCCGTCCGCTCTGCTTCCTCCGCCGGGGCCTTCGACCTGGAGCAGGTGAAGCGTTC T G POLRMT Ensembl:ENSG00000099821 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:617226..617419 26863410 MeRIP-seq:(Medium) rs531160208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19088247 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_122408,RMVar_hsa_circ_125915,RMVar_hsa_circ_128093,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_105438,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190880,RMVar_hsa_circ_190882,RMVar_hsa_circ_190881,RMVar_hsa_circ_190879,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869 80019 RMVar_ID_80019 Human_SNP_ID_655093544 m1A Human chr19 - 618055 618055 618055 GCAGCGTGGGGGGCGGCAGGGGTGGGGCGAGGAGGCTTCTGGGAACATTTCCTCCCCCTGTACTG GCAGCGTGGGGGGCGGCAGGGGTGGGGCGAGGCGGCTTCTGGGAACATTTCCTCCCCCTGTACTG T G POLRMT Ensembl:ENSG00000099821 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:618052..618158 26863196 MeRIP-seq:(Medium) rs970370436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203734,Human_RBP_ID_906859,Human_RBP_ID_3955666 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_128093,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_105438,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190880,RMVar_hsa_circ_190879,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_106604,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_63512,RMVar_hsa_circ_87880,RMVar_hsa_circ_190884,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80020 RMVar_ID_80020 Human_SNP_ID_655094648 m1A Human chr19 - 619666 619657 619666 TCACCCGCAAGGTGGTGAAGCAGACGGTGATGACGGTGGTGTACGGGGTCACGCGCTATGGCGGG TCACCCGCAAGGTGGTGAAGCAGACGGTGATG_________TACGGGGTCACGCGCTATGGCGGG ACACCACCGT A POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:619640..619715 26863196 MeRIP-seq:(Medium) rs1487058705 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_8838294,Human_RBP_ID_27472404 Human_Splice_Rec_1928636,Human_Splice_Rec_1928637 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_106604,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190884,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80021 RMVar_ID_80021 Human_SNP_ID_655094652 m1A Human chr19 - 619666 619663 619666 TCACCCGCAAGGTGGTGAAGCAGACGGTGATGACGGTGGTGTACGGGGTCACGCGCTATGGCGGG TCACCCGCAAGGTGGTGAAGCAGACGGTGATG___GTGGTGTACGGGGTCACGCGCTATGGCGGG CCGT C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:619640..619715 26863196 MeRIP-seq:(Medium) rs1187575385 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8838294,Human_RBP_ID_27472404 Human_Splice_Rec_1928636,Human_Splice_Rec_1928637 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_106604,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190884,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80022 RMVar_ID_80022 Human_SNP_ID_655094657 m1A Human chr19 - 619666 619666 619666 TCACCCGCAAGGTGGTGAAGCAGACGGTGATGACGGTGGTGTACGGGGTCACGCGCTATGGCGGG TCACCCGCAAGGTGGTGAAGCAGACGGTGATGGCGGTGGTGTACGGGGTCACGCGCTATGGCGGG T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:619640..619715 26863196 MeRIP-seq:(Medium) rs1167994734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8838294,Human_RBP_ID_27472404 Human_Splice_Rec_1928636,Human_Splice_Rec_1928637 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_106604,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190884,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80023 RMVar_ID_80023 Human_SNP_ID_655094662 m1A Human chr19 - 619675 619675 619675 AAGGTTTCATCACCCGCAAGGTGGTGAAGCAGACGGTGATGACGGTGGTGTACGGGGTCACGCGC AAGGTTTCATCACCCGCAAGGTGGTGAAGCAGGCGGTGATGACGGTGGTGTACGGGGTCACGCGC T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:619576..619741 26863196 MeRIP-seq:(Medium) rs1163638790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17933411 Human_Splice_Rec_1928636,Human_Splice_Rec_1928637 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_92443,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_109393,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_190878,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190877,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_106604,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190884,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80024 RMVar_ID_80024 Human_SNP_ID_655096100 m1A Human chr19 - 621453 621453 621453 CGCCCCAGCCGCCCGAGGCCCACCTGCCGCACAGCGCCGCGCCCGCCCGCAAGGCCGAGCTGCGC CGCCCCAGCCGCCCGAGGCCCACCTGCCGCACGGCGCCGCGCCCGCCCGCAAGGCCGAGCTGCGC T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:621432..621521 26863196 MeRIP-seq:(Medium) rs1198840307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239421,Human_RBP_ID_22447082 Human_miRNA_ID_2077255 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80025 RMVar_ID_80025 Human_SNP_ID_655096153 m1A Human chr19 - 621515 621515 621515 GCTGCAGCTCTTCCAGGCCAAGGGCTGCCCCCAGCTAGGCGTGCCGGCCCCGCCCTCCGAGGCGC GCTGCAGCTCTTCCAGGCCAAGGGCTGCCCCCCGCTAGGCGTGCCGGCCCCGCCCTCCGAGGCGC T G POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:621334..621583 32194978 MeRIP-seq:(Medium) rs912033372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909873,Human_RBP_ID_3955668,Human_RBP_ID_5116454,Human_RBP_ID_5239485,Human_RBP_ID_9293086,Human_RBP_ID_18470340,Human_RBP_ID_22447082 Human_miRNA_ID_2686006,Human_miRNA_ID_2988704,Human_miRNA_ID_3022403,Human_miRNA_ID_3066317 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80026 RMVar_ID_80026 Human_SNP_ID_655096332 m1A Human chr19 - 621760 621760 621760 GAGCCCACGCTGACCTTCGAGGCGGTGGATGTACCCATGCTTTGCCCCCCGCTGCCCTGGACATC GAGCCCACGCTGACCTTCGAGGCGGTGGATGTTCCCATGCTTTGCCCCCCGCTGCCCTGGACATC T A POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:621733..621830 26863196 MeRIP-seq:(Medium) rs1446917907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22448074 Human_Splice_Rec_1928630 Human_miRNA_ID_2432082 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80027 RMVar_ID_80027 Human_SNP_ID_655096333 m1A Human chr19 - 621760 621760 621760 GAGCCCACGCTGACCTTCGAGGCGGTGGATGTACCCATGCTTTGCCCCCCGCTGCCCTGGACATC GAGCCCACGCTGACCTTCGAGGCGGTGGATGTGCCCATGCTTTGCCCCCCGCTGCCCTGGACATC T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:621733..621830 26863196 MeRIP-seq:(Medium) rs1446917907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22448074 Human_Splice_Rec_1928630 Human_miRNA_ID_2432082 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80028 RMVar_ID_80028 Human_SNP_ID_655096367 m1A Human chr19 - 621800 621800 621800 GCCGCACCCGGCCTACGTGCAGCTGCTGGAGAAGGCCGCGGAGCCCACGCTGACCTTCGAGGCGG GCCGCACCCGGCCTACGTGCAGCTGCTGGAGATGGCCGCGGAGCCCACGCTGACCTTCGAGGCGG T A POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:621781..622234 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18995547 Human_Splice_Rec_1928630 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_112936,RMVar_hsa_circ_123769,RMVar_hsa_circ_116116,RMVar_hsa_circ_107068,RMVar_hsa_circ_87843,RMVar_hsa_circ_91626,RMVar_hsa_circ_85833,RMVar_hsa_circ_190874,RMVar_hsa_circ_77027,RMVar_hsa_circ_190876,RMVar_hsa_circ_190875,RMVar_hsa_circ_190872,RMVar_hsa_circ_190873,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886 80029 RMVar_ID_80029 Human_SNP_ID_655097987 m1A Human chr19 - 624790 624790 624790 CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCACCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCGCCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:624788..624875 26863196 MeRIP-seq:(Medium) rs770914181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293089,Human_RBP_ID_9327915,Human_RBP_ID_22533048 Human_Splice_Rec_1928621,Human_Splice_Rec_1928685,Human_Splice_Rec_1928695 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_116116,RMVar_hsa_circ_87843,RMVar_hsa_circ_85833,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886,RMVar_hsa_circ_54408 80030 RMVar_ID_80030 Human_SNP_ID_655097988 m1A Human chr19 - 624790 624790 624790 CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCACCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCCCCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG T G POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:624788..624875 26863196 MeRIP-seq:(Medium) rs770914181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293089,Human_RBP_ID_9327915,Human_RBP_ID_22533048 Human_Splice_Rec_1928621,Human_Splice_Rec_1928685,Human_Splice_Rec_1928695 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_116116,RMVar_hsa_circ_87843,RMVar_hsa_circ_85833,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886,RMVar_hsa_circ_54408 80031 RMVar_ID_80031 Human_SNP_ID_655100285 m1A Human chr19 + 630114 630112 630115 ATTCTGGGAGCCGCGCCACATCCACCCTGTTCACCACCACCTCCGACACGCTCTCAGCCTGCAGC ATTCTGGGAGCCGCGCCACATCCACCCTGTT___CACCACCTCCGACACGCTCTCAGCCTGCAGC TCAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:629984..633604 26863196 MeRIP-seq:(Medium) rs1426801437 Functional Loss DEL dbSNP153 32..34 33 - - - 80032 RMVar_ID_80032 Human_SNP_ID_655100286 m1A Human chr19 + 630114 630114 630114 ATTCTGGGAGCCGCGCCACATCCACCCTGTTCACCACCACCTCCGACACGCTCTCAGCCTGCAGC ATTCTGGGAGCCGCGCCACATCCACCCTGTTCCCCACCACCTCCGACACGCTCTCAGCCTGCAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:629984..633604 26863196 MeRIP-seq:(Medium) rs1333643591 Functional Loss SNV dbSNP153 33..33 33 - - - 80033 RMVar_ID_80033 Human_SNP_ID_655100290 m1A Human chr19 - 630123 630120 630123 GGTGCGGCAGCTGCAGGCTGAGAGCGTGTCGGAGGTGGTGGTGAACAGGGTGGATGTGGCGCGGC GGTGCGGCAGCTGCAGGCTGAGAGCGTGTCGG___TGGTGGTGAACAGGGTGGATGTGGCGCGGC ACCT A POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:629975..633206 26863196 MeRIP-seq:(Medium) rs1568176691 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_826037,Human_RBP_ID_4553172,Human_RBP_ID_17696599 Human_Splice_Rec_1928616,Human_Splice_Rec_1928700 Human_miRNA_ID_1951026,Human_miRNA_ID_1952314,Human_miRNA_ID_1979583,Human_miRNA_ID_2172460 RMVar_hsa_circ_82052,RMVar_hsa_circ_116116,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_87880,RMVar_hsa_circ_190886,RMVar_hsa_circ_54408 80034 RMVar_ID_80034 Human_SNP_ID_655100291 m1A Human chr19 - 630123 630123 630123 GGTGCGGCAGCTGCAGGCTGAGAGCGTGTCGGAGGTGGTGGTGAACAGGGTGGATGTGGCGCGGC GGTGCGGCAGCTGCAGGCTGAGAGCGTGTCGGTGGTGGTGGTGAACAGGGTGGATGTGGCGCGGC T A POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:629975..633206 26863196 MeRIP-seq:(Medium) rs890378410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826037,Human_RBP_ID_4553172,Human_RBP_ID_17696599 Human_Splice_Rec_1928616,Human_Splice_Rec_1928700 Human_miRNA_ID_1951026,Human_miRNA_ID_1952314,Human_miRNA_ID_1979583,Human_miRNA_ID_2172460 RMVar_hsa_circ_82052,RMVar_hsa_circ_116116,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_87880,RMVar_hsa_circ_190886,RMVar_hsa_circ_54408 80035 RMVar_ID_80035 Human_SNP_ID_655101761 m1A Human chr19 + 633376 633348 633376 AAAGCGCCAAAGGCCCCGGCCGCGCGGGGAGGAGCCCACGCCGTGGCCCCCGGGCTGCCTGGCCG AAAGC____________________________GCCCACGCCGTGGCCCCCGGGCTGCCTGGCCG CGCCAAAGGCCCCGGCCGCGCGGGGAGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:633373..633505 26863196 MeRIP-seq:(Medium) rs923251394 Functional Loss DEL dbSNP153 6..33 33 - - - 80036 RMVar_ID_80036 Human_SNP_ID_655102139 m1A Human chr19 - 634031 634031 634031 AAGTTGTCGTTGGAGCAATGAAGGTTGCGGACAGGAATCTCTAAATTGCAGATGCTGTCCTCGTT AAGTTGTCGTTGGAGCAATGAAGGTTGCGGACGGGAATCTCTAAATTGCAGATGCTGTCCTCGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:634025..634202 26863196 MeRIP-seq:(Medium) rs182276455 Functional Loss SNV dbSNP153 33..33 33 - - - 80037 RMVar_ID_80037 Human_SNP_ID_655103235 m1A Human chr19 + 637731 637731 637731 GGCGTGAAAAGGAGCAAGGCTCTGCCCCAGCCACAGCGCGGATGCACCTTGAGGATGTCATGCTC GGCGTGAAAAGGAGCAAGGCTCTGCCCCAGCCGCAGCGCGGATGCACCTTGAGGATGTCATGCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:637729..637905 26863196 MeRIP-seq:(Medium) rs566846701 Functional Loss SNV dbSNP153 33..33 33 - - - 80038 RMVar_ID_80038 Human_SNP_ID_655103767 m1A Human chr19 - 639472 639472 639472 AAGAGACACAAGGAAGATGACCGGGAGAGACGAGAGAGACACAGAGACAGAGAGGGGCAGAGGCG AAGAGACACAAGGAAGATGACCGGGAGAGACGCGAGAGACACAGAGACAGAGAGGGGCAGAGGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:639446..639618 26863196 MeRIP-seq:(Medium) rs1177458992 Functional Loss SNV dbSNP153 33..33 33 - - - 80039 RMVar_ID_80039 Human_SNP_ID_655104104 m1A Human chr19 + 640190 640190 640190 GGGCCTGGGGTGGGGAGGCGGCGGGTGACGGCAACGCGGCCGCCGTCTTCACGGTGACCTGCGCC GGGCCTGGGGTGGGGAGGCGGCGGGTGACGGCTACGCGGCCGCCGTCTTCACGGTGACCTGCGCC A T FGF22 Ensembl:ENSG00000070388 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:640185..640871 26863196 MeRIP-seq:(Medium) rs1225805572 Functional Loss SNV dbSNP153 33..33 33 - - - 80040 RMVar_ID_80040 Human_SNP_ID_655105096 m1A Human chr19 - 642570 642570 642570 GAGCCCCCAGCCCGGCCCTCACAGCTCACACCACCCCAGGGACCCCCCAGCCCGGCCCTCACAGC GAGCCCCCAGCCCGGCCCTCACAGCTCACACCCCCCCAGGGACCCCCCAGCCCGGCCCTCACAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:642567..642656 26863196 MeRIP-seq:(Medium) rs1341321207 Functional Loss SNV dbSNP153 33..33 33 - - - 80041 RMVar_ID_80041 Human_SNP_ID_655106854 m1A Human chr19 - 646242 646242 646242 TGCAGCGGCGGGACCTGGAGACTCGGAACTGGAGGGCCTTTGTCAGAGATGCTGCCGGGGTGTGC TGCAGCGGCGGGACCTGGAGACTCGGAACTGGGGGGCCTTTGTCAGAGATGCTGCCGGGGTGTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:646237..646347 26863196 MeRIP-seq:(Medium) rs538044839 Functional Loss SNV dbSNP153 33..33 33 - - - 80042 RMVar_ID_80042 Human_SNP_ID_655107629 m1A Human chr19 - 647972 647964 647972 GCCTGTTCCAGGGCAGGACCCGGGCCCGGCCCACCGGCCCCCTGGCTTGGGAAGGCGTGGGCCAC GCCTGTTCCAGGGCAGGACCCGGGCCCGGCCC________CCTGGCTTGGGAAGGCGTGGGCCAC GGGGCCGGT G RNF126 Ensembl:ENSG00000070423 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:647924..648963 32194978 MeRIP-seq:(Medium) rs1369096007 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_4553705,Human_RBP_ID_22069335 80043 RMVar_ID_80043 Human_SNP_ID_655107723 m1A Human chr19 - 648142 648142 648142 CCTCCTCCAGCTCGCCCAGCAACGAGAACGCCACAAGCAACTCGTGAGCCCACGTCGGCCGTCGG CCTCCTCCAGCTCGCCCAGCAACGAGAACGCCGCAAGCAACTCGTGAGCCCACGTCGGCCGTCGG T C RNF126 Ensembl:ENSG00000070423 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:648117..648282 26863196 MeRIP-seq:(Medium) rs1391849051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26470882,Human_RBP_ID_27472576 80044 RMVar_ID_80044 Human_SNP_ID_655109868 m1A Human chr19 - 652513 652513 652513 ACGGGGGCCCTACCCACATTCTCACGCTTAGGAGGCTGTTGGGGTCTGCACCGGTTTATCGAGAA ACGGGGGCCCTACCCACATTCTCACGCTTAGGGGGCTGTTGGGGTCTGCACCGGTTTATCGAGAA T C RNF126 Ensembl:ENSG00000070423 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:652512..652713 32194978 MeRIP-seq:(Medium) rs886471658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13531935 RMVar_hsa_circ_378992,RMVar_hsa_circ_299964,RMVar_hsa_circ_292020,RMVar_hsa_circ_190888 80045 RMVar_ID_80045 Human_SNP_ID_655113193 m1A Human chr19 - 661605 661603 661605 GAGCGAGTGCTAGAGTTGGGGCATGGCGGGAGAGCGGGGCCAGGCCCAGGAGTGGAAAGAGAGAG GAGCGAGTGCTAGAGTTGGGGCATGGCGGGAG__CGGGGCCAGGCCCAGGAGTGGAAAGAGAGAG GCT G RNF126 Ensembl:ENSG00000070423 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:661596..661726 26863196 MeRIP-seq:(Medium) rs1216942939 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7911,Human_RBP_ID_3579669,Human_RBP_ID_5320654,Human_RBP_ID_8098905,Human_RBP_ID_8232885,Human_RBP_ID_18421029,Human_RBP_ID_18488426,Human_RBP_ID_20433154,Human_RBP_ID_22416510,Human_RBP_ID_22719430,Human_RBP_ID_22742077,Human_RBP_ID_23279390,Human_RBP_ID_24374360,Human_RBP_ID_24552707,Human_RBP_ID_26336887 80046 RMVar_ID_80046 Human_SNP_ID_655113827 m1A Human chr19 - 663138 663138 663138 GGCGGGTGCCGCGCGGGGGGCGGGCGGCGCGGAGTAGGTGGCGGCGGCCATGGCCGAGGCGTCGC GGCGGGTGCCGCGCGGGGGGCGGGCGGCGCGGTGTAGGTGGCGGCGGCCATGGCCGAGGCGTCGC T A RNF126 Ensembl:ENSG00000070423 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:663026..663200;chr19:662776..663225;chr19:652826..663227 26863410,26863196,26863196 MeRIP-seq:(Medium) rs569152546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4553803,Human_RBP_ID_9329283,Human_RBP_ID_17933622,Human_RBP_ID_18421034 Human_Splice_Rec_1928709,Human_Splice_Rec_1928725,Human_Splice_Rec_1928763,Human_Splice_Rec_1928779,Human_Splice_Rec_1928785 80047 RMVar_ID_80047 Human_SNP_ID_655118528 m1A Human chr19 - 676414 676414 676414 GGCCCTGGCGCCCCGGGACGCATGGCGAACGCAGAGACGGCAGCGGCACCGACTTCCCAGCGCGC GGCCCTGGCGCCCCGGGACGCATGGCGAACGCGGAGACGGCAGCGGCACCGACTTCCCAGCGCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:676401..676630 26863196 MeRIP-seq:(Medium) rs1440888894 Functional Loss SNV dbSNP153 33..33 33 - - - 80048 RMVar_ID_80048 Human_SNP_ID_655118796 m1A Human chr19 - 676998 676998 676998 CGTCTCCTGCCTGGCACCTCCCGGCAAGTCCCAGGTGTGAGACTCCATGCCCCGTCTACCCAGGA CGTCTCCTGCCTGGCACCTCCCGGCAAGTCCCCGGTGTGAGACTCCATGCCCCGTCTACCCAGGA T G lnc-PRSS57-1 RNACentral:URS0000D5A503 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:676996..677108 26863196 MeRIP-seq:(Medium) rs1269211670 Functional Loss SNV dbSNP153 33..33 33 - - - 80049 RMVar_ID_80049 Human_SNP_ID_655119142 m1A Human chr19 - 677888 677888 677888 CCGGGTGGGTGAGGTTGGACCAGGCGGTGTCAATGTTGCCGGAGGCACAGCACTCGGCCCGGGTG CCGGGTGGGTGAGGTTGGACCAGGCGGTGTCAGTGTTGCCGGAGGCACAGCACTCGGCCCGGGTG T C lnc-PRSS57-1 RNACentral:URS0000D5A503 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:677876..678043 26863196 MeRIP-seq:(Medium) rs755229140 Functional Loss SNV dbSNP153 33..33 33 - - - 80050 RMVar_ID_80050 Human_SNP_ID_655119273 m1A Human chr19 - 678207 678207 678207 GGAAGAGCCACCCAGGCAGAGAGCTCAGCCCCAGCAAAGGCTGGAGCCACGTGGTCTCTTCCTGA GGAAGAGCCACCCAGGCAGAGAGCTCAGCCCCGGCAAAGGCTGGAGCCACGTGGTCTCTTCCTGA T C lnc-PRSS57-1 RNACentral:URS0000D5A503 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:678205..678383 32194978 MeRIP-seq:(Medium) rs1242331752 Functional Loss SNV dbSNP153 33..33 33 - - - 80051 RMVar_ID_80051 Human_SNP_ID_655119545 m1A Human chr19 + 678840 678840 678840 GCCTGTTGGGGCACATCTTGAAGGAGGTGGGCATTAGAGCTGGGGTGTTGGGGGATGTCTAGGAG GCCTGTTGGGGCACATCTTGAAGGAGGTGGGCCTTAGAGCTGGGGTGTTGGGGGATGTCTAGGAG A C FSTL3 Ensembl:ENSG00000070404 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:678826..679043 26863196 MeRIP-seq:(Medium) rs963112314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116465,RMVar_hsa_circ_105836,RMVar_hsa_circ_190889,RMVar_hsa_circ_190890 80052 RMVar_ID_80052 Human_SNP_ID_655120362 m1A Human chr19 - 680772 680772 680772 ACTCCCTCGGAAGTATAAAGACGCCCTTACTCAGGCCCCACCGCCACCCATGTGACCTGTCCTGG ACTCCCTCGGAAGTATAAAGACGCCCTTACTCGGGCCCCACCGCCACCCATGTGACCTGTCCTGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:680757..681120 26863196 MeRIP-seq:(Medium) rs1398134289 Functional Loss SNV dbSNP153 33..33 33 - - - 80053 RMVar_ID_80053 Human_SNP_ID_655120505 m1A Human chr19 + 681182 681182 681182 GGCTTGTGGGTGGAGCCTGAGGGGTGGAATGGAGAGGGGGGCTCACGGGGGGCGGGGGGGTGCTT GGCTTGTGGGTGGAGCCTGAGGGGTGGAATGGGGAGGGGGGCTCACGGGGGGCGGGGGGGTGCTT A G FSTL3 Ensembl:ENSG00000070404 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:681176..681225 26863196 MeRIP-seq:(Medium) rs1261651411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116465,RMVar_hsa_circ_109455,RMVar_hsa_circ_105836,RMVar_hsa_circ_190889,RMVar_hsa_circ_190890,RMVar_hsa_circ_190891 80054 RMVar_ID_80054 Human_SNP_ID_655120624 m1A Human chr19 + 681450 681450 681450 GGCGCCCTGCCCTGTGCCCTCCAGCCCCGGCCAGGAGCTTTGCGGCAACAACAACGTCACCTACA GGCGCCCTGCCCTGTGCCCTCCAGCCCCGGCCGGGAGCTTTGCGGCAACAACAACGTCACCTACA A G FSTL3 Ensembl:ENSG00000070404 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:681401..681500 32194978 MeRIP-seq:(Medium) rs759339088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22763535 RMVar_hsa_circ_116465,RMVar_hsa_circ_109455,RMVar_hsa_circ_105836,RMVar_hsa_circ_190889,RMVar_hsa_circ_190890,RMVar_hsa_circ_88368,RMVar_hsa_circ_190891,RMVar_hsa_circ_190892 80055 RMVar_ID_80055 Human_SNP_ID_655120653 m1A Human chr19 + 681504 681504 681504 CGTCACCTACATCTCCTCGTGCCACATGCGCCAGGCCACCTGCTTCCTGGGCCGCTCCATCGGCG CGTCACCTACATCTCCTCGTGCCACATGCGCCTGGCCACCTGCTTCCTGGGCCGCTCCATCGGCG A T FSTL3 Ensembl:ENSG00000070404 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:681326..681613 26863196 MeRIP-seq:(Medium) rs1568203763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22763536 Human_Splice_Rec_1928795,Human_Splice_Rec_1928801,Human_Splice_Rec_1928807,Human_Splice_Rec_1928811,Human_Splice_Rec_1928817 RMVar_hsa_circ_116465,RMVar_hsa_circ_109455,RMVar_hsa_circ_105836,RMVar_hsa_circ_190889,RMVar_hsa_circ_190890,RMVar_hsa_circ_88368,RMVar_hsa_circ_190891,RMVar_hsa_circ_190892 80056 RMVar_ID_80056 Human_SNP_ID_655120804 m1A Human chr19 - 681767 681767 681767 CCGTGGCATATAAATTAGACTCTGCTGTGGCAATAAATAACAGGGGATGATGGGGGGCCTCGGGC CCGTGGCATATAAATTAGACTCTGCTGTGGCACTAAATAACAGGGGATGATGGGGGGCCTCGGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:681635..681953 26863196 MeRIP-seq:(Medium) rs1166212766 Functional Loss SNV dbSNP153 33..33 33 - - - 80057 RMVar_ID_80057 Human_SNP_ID_655120999 m1A Human chr19 - 682253 682253 682253 GACCCTCCATACTCACCCAGGCTAGATCCTCCATACACACCCAGGCTAGACCCTCCGTACTCACC GACCCTCCATACTCACCCAGGCTAGATCCTCCGTACACACCCAGGCTAGACCCTCCGTACTCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:682078..682325;chr19:682110..682325 26863196 MeRIP-seq:(Medium) rs1179266563 Functional Loss SNV dbSNP153 33..33 33 - - - 80058 RMVar_ID_80058 Human_SNP_ID_655121303 m1A Human chr19 + 683182 683182 683182 CACAGCCTCAGACCAGCTATGGGGAGAGGACAACACGGAGGATATCCAGCTTCCCCGGTCTGGGG CACAGCCTCAGACCAGCTATGGGGAGAGGACATCACGGAGGATATCCAGCTTCCCCGGTCTGGGG A T FSTL3 Ensembl:ENSG00000070404 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:683133..683241 26863196 MeRIP-seq:(Medium) rs1428121973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2000774 RMVar_hsa_circ_89011,RMVar_hsa_circ_116465,RMVar_hsa_circ_109455,RMVar_hsa_circ_105836,RMVar_hsa_circ_190889,RMVar_hsa_circ_190890,RMVar_hsa_circ_88368,RMVar_hsa_circ_190891,RMVar_hsa_circ_190892,RMVar_hsa_circ_190893 80059 RMVar_ID_80059 Human_SNP_ID_655121311 m1A Human chr19 - 683210 683210 683210 AGGATGCCCAAGCTCCCCACATTCCTCACCCCAGACCGGGGAAGCTGGATATCCTCCGTGTTGTC AGGATGCCCAAGCTCCCCACATTCCTCACCCCCGACCGGGGAAGCTGGATATCCTCCGTGTTGTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:683201..683250 26863196 MeRIP-seq:(Medium) rs1251622685 Functional Loss SNV dbSNP153 33..33 33 - - - 80060 RMVar_ID_80060 Human_SNP_ID_655132604 m1A Human chr19 + 715571 715571 715571 TTGTGGAAGGACTGGCATGTGCAAAGGGCTAGAGGTGGGAAAGCATTGGAAGAAGAGAATGCTCT TTGTGGAAGGACTGGCATGTGCAAAGGGCTAGGGGTGGGAAAGCATTGGAAGAAGAGAATGCTCT A G PALM Ensembl:ENSG00000099864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:715569..715778 26863196 MeRIP-seq:(Medium) rs1457344603 Functional Loss SNV dbSNP153 33..33 33 - - - 80061 RMVar_ID_80061 Human_SNP_ID_655133962 m1A Human chr19 - 719817 719817 719817 GGGTCAGCCCCATTTCACCGACGGGGAAACTGAGGCCGGGCAGGGCGGCCTTCTCCCGGCGTTCA GGGTCAGCCCCATTTCACCGACGGGGAAACTGCGGCCGGGCAGGGCGGCCTTCTCCCGGCGTTCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:719813..719925 32194978 MeRIP-seq:(Medium) rs1364808878 Functional Loss SNV dbSNP153 33..33 33 - - - 80062 RMVar_ID_80062 Human_SNP_ID_655135149 m1A Human chr19 + 722853 722853 722853 CTGAACCCAGCCTCCCTGAGGAGGGAGAAGGGAAAGCCACAGAGGGCGCAGCTGGTGTTCCCGGG CTGAACCCAGCCTCCCTGAGGAGGGAGAAGGGGAAGCCACAGAGGGCGCAGCTGGTGTTCCCGGG A G PALM Ensembl:ENSG00000099864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:722849..723078 26863196 MeRIP-seq:(Medium) rs1381008112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928889 80063 RMVar_ID_80063 Human_SNP_ID_655136194 m1A Human chr19 + 726179 726179 726179 GGCAGAGACCACGTCCCAGCAGGAGCGGCTGCAGGCCATCGCAGTGAGTTTCCGCCGCCCCGCAG GGCAGAGACCACGTCCCAGCAGGAGCGGCTGCCGGCCATCGCAGTGAGTTTCCGCCGCCCCGCAG A C PALM Ensembl:ENSG00000099864 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:726169..726254 26863196 MeRIP-seq:(Medium) rs752641621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18995564 Human_Splice_Rec_1928836,Human_Splice_Rec_1928837,Human_Splice_Rec_1928852,Human_Splice_Rec_1928853,Human_Splice_Rec_1928866,Human_Splice_Rec_1928867,Human_Splice_Rec_1928876,Human_Splice_Rec_1928877,Human_Splice_Rec_1928888,Human_Splice_Rec_1928890,Human_Splice_Rec_1928891 RMVar_hsa_circ_190896,RMVar_hsa_circ_269362,RMVar_hsa_circ_323575,RMVar_hsa_circ_325908,RMVar_hsa_circ_321537,RMVar_hsa_circ_43297,RMVar_hsa_circ_90095,RMVar_hsa_circ_190897,RMVar_hsa_circ_190895 80064 RMVar_ID_80064 Human_SNP_ID_655138093 m1A Human chr19 + 731050 731050 731050 GGAGCTGTCGTACAGAAGGTGCCCAGAGCCCCACCGGGGATGCAGGAGTCACCCTCACAGGCACA GGAGCTGTCGTACAGAAGGTGCCCAGAGCCCCTCCGGGGATGCAGGAGTCACCCTCACAGGCACA A T PALM Ensembl:ENSG00000099864 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:731049..731250 26863196 MeRIP-seq:(Medium) rs761193548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269362,RMVar_hsa_circ_323575,RMVar_hsa_circ_321537,RMVar_hsa_circ_43297,RMVar_hsa_circ_190897 80065 RMVar_ID_80065 Human_SNP_ID_655140321 m1A Human chr19 - 737780 737780 737780 CATCATCTCTCCTCCGCCCTCTCCCCCTCCTCACGCTGCTCCAGCCACACGGATCTCCTGGCCGT CATCATCTCTCCTCCGCCCTCTCCCCCTCCTCCCGCTGCTCCAGCCACACGGATCTCCTGGCCGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:737525..738173 26863196 MeRIP-seq:(Medium) rs1234247789 Functional Loss SNV dbSNP153 33..33 33 - - - 80066 RMVar_ID_80066 Human_SNP_ID_655141626 m1A Human chr19 + 741554 741554 741554 GGTGAGGGGAGACGGGCTGCAGGGGTGAGGGGAGACGGGCTGCAGGGGTGAGGGGGAACCAGGTT GGTGAGGGGAGACGGGCTGCAGGGGTGAGGGGGGACGGGCTGCAGGGGTGAGGGGGAACCAGGTT A G PALM Ensembl:ENSG00000099864 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:741549..741770 26863196 MeRIP-seq:(Medium) rs1046883582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8194824 80067 RMVar_ID_80067 Human_SNP_ID_655141636 m1A Human chr19 - 741570 741570 741570 CCTCAACTCCCTGACCAACCTGGTTCCCCCTCACCCCTGCAGCCCGTCTCCCCTCACCCCTGCAG CCTCAACTCCCTGACCAACCTGGTTCCCCCTCCCCCCTGCAGCCCGTCTCCCCTCACCCCTGCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:741565..741651 26863196 MeRIP-seq:(Medium) rs1439234182 Functional Loss SNV dbSNP153 33..33 33 - - - 80068 RMVar_ID_80068 Human_SNP_ID_655143373 m1A Human chr19 + 746732 746732 746732 TCCCACGGAGGCCGCCTCCAGGGAAGAGAATCAGGCGGGGCCCGAGGCCACCACCAGCGACCCCC TCCCACGGAGGCCGCCTCCAGGGAAGAGAATCGGGCGGGGCCCGAGGCCACCACCAGCGACCCCC A G PALM Ensembl:ENSG00000099864 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:746686..746788 26863196 MeRIP-seq:(Medium) rs1278402622 Functional Loss SNV dbSNP153 33..33 33 - - - 80069 RMVar_ID_80069 Human_SNP_ID_655145421 m1A Human chr19 - 753026 753026 753026 GGCCTCGCTCTCGCCTGCTGTGGCCACAGGTCAGCACCCTTCCTGCAGCCCAGAGTCTGGTATAC GGCCTCGCTCTCGCCTGCTGTGGCCACAGGTCGGCACCCTTCCTGCAGCCCAGAGTCTGGTATAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:753024..753131 26863196 MeRIP-seq:(Medium) rs1019330017 Functional Loss SNV dbSNP153 33..33 33 - - - 80070 RMVar_ID_80070 Human_SNP_ID_655145943 m1A Human chr19 + 754642 754642 754642 CAGCGAGACTCTGTCTCAAAACAAAAGACAATACCTAAGACGGGTGCTGGGTACAAGGCCTGACA CAGCGAGACTCTGTCTCAAAACAAAAGACAATGCCTAAGACGGGTGCTGGGTACAAGGCCTGACA A G MISP Ensembl:ENSG00000099812 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:754639..755203 26863196 MeRIP-seq:(Medium) rs777602501 Functional Loss SNV dbSNP153 33..33 33 - - - 80071 RMVar_ID_80071 Human_SNP_ID_655146812 m1A Human chr19 + 757389 757389 757389 TGACCTGGAGCGGGAGCGCTGGGCCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCAGCACCGTGG TGACCTGGAGCGGGAGCGCTGGGCCGTCATCCGGGGCCAGGCAGTCAGGAAGAGCAGCACCGTGG A G MISP Ensembl:ENSG00000099812 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:757347..757420 26863196 MeRIP-seq:(Medium) rs1452542204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314961 80072 RMVar_ID_80072 Human_SNP_ID_655146827 m1A Human chr19 + 757412 757412 757412 CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCAGCACCGTGGCCACGCTCCAGGGCACTCCTGAC CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCCGCACCGTGGCCACGCTCCAGGGCACTCCTGAC A C MISP Ensembl:ENSG00000099812 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:757150..757614 26863196 MeRIP-seq:(Medium) rs3746173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314961 80073 RMVar_ID_80073 Human_SNP_ID_655146828 m1A Human chr19 + 757412 757412 757412 CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCAGCACCGTGGCCACGCTCCAGGGCACTCCTGAC CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCGGCACCGTGGCCACGCTCCAGGGCACTCCTGAC A G MISP Ensembl:ENSG00000099812 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:757150..757614 26863196 MeRIP-seq:(Medium) rs3746173 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_314961 80074 RMVar_ID_80074 Human_SNP_ID_655149167 m1A Human chr19 + 763532 763532 763532 GGTCCTGGAAGCCATACGGGTGACCCGTCACAAGAACGCCATGGCAGAGCGCTGGGAATCCCGCA GGTCCTGGAAGCCATACGGGTGACCCGTCACAGGAACGCCATGGCAGAGCGCTGGGAATCCCGCA A G MISP Ensembl:ENSG00000099812 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:763524..763675 26863196 MeRIP-seq:(Medium) rs1470046113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928932 RMVar_hsa_circ_114695,RMVar_hsa_circ_190901 80075 RMVar_ID_80075 Human_SNP_ID_655149200 m1A Human chr19 - 763594 763594 763594 AGGGCAGGGCAGGGGGTGGGCGCCCCATCCCGAGGCTCAGTCATCCTCCTCACTGGCGTAGATGC AGGGCAGGGCAGGGGGTGGGCGCCCCATCCCGCGGCTCAGTCATCCTCCTCACTGGCGTAGATGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:763543..763692 26863196 MeRIP-seq:(Medium) rs761046299 Functional Loss SNV dbSNP153 33..33 33 - - - 80076 RMVar_ID_80076 Human_SNP_ID_655149203 m1A Human chr19 - 763600 763600 763600 AGGGTCAGGGCAGGGCAGGGGGTGGGCGCCCCATCCCGAGGCTCAGTCATCCTCCTCACTGGCGT AGGGTCAGGGCAGGGCAGGGGGTGGGCGCCCCTTCCCGAGGCTCAGTCATCCTCCTCACTGGCGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:763551..763667 26863196 MeRIP-seq:(Medium) rs1169502781 Functional Loss SNV dbSNP153 33..33 33 - - - 80077 RMVar_ID_80077 Human_SNP_ID_655151995 m1A Human chr19 - 772036 772030 772036 AGAGAGGGGACTGGGCAGAGGGGGAGACAGGGAAGAGGGAGAGGAGAGAGGGGACTGGGCAGAGG AGAGAGGGGACTGGGCAGAGGGGGAGACAGGG______GAGAGGAGAGAGGGGACTGGGCAGAGG CCCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:772029..772397 26863196 MeRIP-seq:(Medium) rs1193711326 Functional Loss DEL dbSNP153 33..38 33 - - - 80078 RMVar_ID_80078 Human_SNP_ID_655152014 m1A Human chr19 - 772084 772082 772084 TAGAGAGGGGACTGGGCAGAGGAGGGGGAGACAGGGAGGAGGGAGAGGAGAGAGGGGACTGGGCA TAGAGAGGGGACTGGGCAGAGGAGGGGGAGAC__GGAGGAGGGAGAGGAGAGAGGGGACTGGGCA CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:772075..772316 26863196 MeRIP-seq:(Medium) rs1193171500 Functional Loss DEL dbSNP153 33..34 33 - - - 80079 RMVar_ID_80079 Human_SNP_ID_655155970 m1A Human chr19 - 782462 782462 782462 ACCCCGAGCCTCACTCGTGCCACCGGCCACCCAGCGTCCCCTGCATCTTCCCCGGGGACTCACAC ACCCCGAGCCTCACTCGTGCCACCGGCCACCCGGCGTCCCCTGCATCTTCCCCGGGGACTCACAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:782416..782582;chr19:782453..782552 26863196 MeRIP-seq:(Medium) rs1168957536 Functional Loss SNV dbSNP153 33..33 33 - - - 80080 RMVar_ID_80080 Human_SNP_ID_655156711 m1A Human chr19 + 784693 784693 784693 GGCGGCTGGTGTGCGGGGTTGGGGACGATGGCAGGGACAGGAGGGAGGTGCTGTTGGCATGTGTG GGCGGCTGGTGTGCGGGGTTGGGGACGATGGCGGGGACAGGAGGGAGGTGCTGTTGGCATGTGTG A G LINC01836 Ensembl:ENSG00000267530 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:784645..784834 26863196 MeRIP-seq:(Medium) rs897871020 Functional Loss SNV dbSNP153 33..33 33 - - - 80081 RMVar_ID_80081 Human_SNP_ID_655161416 m1A Human chr19 + 797466 797466 797466 GTTGGGTCGGTTCCTGCTATTCCGGCGCCTCCACTCCGTCCCCCGCGGGTCTGCTCTGTGTGCCA GTTGGGTCGGTTCCTGCTATTCCGGCGCCTCCCCTCCGTCCCCCGCGGGTCTGCTCTGTGTGCCA A C PTBP1 Ensembl:ENSG00000011304 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:797451..797741 26863196 MeRIP-seq:(Medium) rs753578445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52497,Human_RBP_ID_529375,Human_RBP_ID_769789,Human_RBP_ID_4554823,Human_RBP_ID_5421974,Human_RBP_ID_5443597,Human_RBP_ID_5469350,Human_RBP_ID_5500381,Human_RBP_ID_6793688,Human_RBP_ID_8496710,Human_RBP_ID_8839587,Human_RBP_ID_9327931,Human_RBP_ID_17386499,Human_RBP_ID_17670259,Human_RBP_ID_17933846,Human_RBP_ID_22448078,Human_RBP_ID_23811440,Human_RBP_ID_26997547,Human_RBP_ID_27157995,Human_RBP_ID_27472741,Human_RBP_ID_27562947 Human_Splice_Rec_1928949,Human_Splice_Rec_1928975,Human_Splice_Rec_1928987,Human_Splice_Rec_1928995,Human_Splice_Rec_1929021,Human_Splice_Rec_1929029,Human_Splice_Rec_1929051,Human_Splice_Rec_1929079,Human_Splice_Rec_1929107,Human_Splice_Rec_1929121 Human_miRNA_ID_2135182 RMVar_hsa_circ_117637,RMVar_hsa_circ_190902 80082 RMVar_ID_80082 Human_SNP_ID_655161417 m1A Human chr19 + 797466 797466 797466 GTTGGGTCGGTTCCTGCTATTCCGGCGCCTCCACTCCGTCCCCCGCGGGTCTGCTCTGTGTGCCA GTTGGGTCGGTTCCTGCTATTCCGGCGCCTCCTCTCCGTCCCCCGCGGGTCTGCTCTGTGTGCCA A T PTBP1 Ensembl:ENSG00000011304 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:797451..797741 26863196 MeRIP-seq:(Medium) rs753578445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52497,Human_RBP_ID_529375,Human_RBP_ID_769789,Human_RBP_ID_4554823,Human_RBP_ID_5421974,Human_RBP_ID_5443597,Human_RBP_ID_5469350,Human_RBP_ID_5500381,Human_RBP_ID_6793688,Human_RBP_ID_8496710,Human_RBP_ID_8839587,Human_RBP_ID_9327931,Human_RBP_ID_17386499,Human_RBP_ID_17670259,Human_RBP_ID_17933846,Human_RBP_ID_22448078,Human_RBP_ID_23811440,Human_RBP_ID_26997547,Human_RBP_ID_27157995,Human_RBP_ID_27472741,Human_RBP_ID_27562947 Human_Splice_Rec_1928949,Human_Splice_Rec_1928975,Human_Splice_Rec_1928987,Human_Splice_Rec_1928995,Human_Splice_Rec_1929021,Human_Splice_Rec_1929029,Human_Splice_Rec_1929051,Human_Splice_Rec_1929079,Human_Splice_Rec_1929107,Human_Splice_Rec_1929121 Human_miRNA_ID_2135182 RMVar_hsa_circ_117637,RMVar_hsa_circ_190902 80083 RMVar_ID_80083 Human_SNP_ID_655161463 m1A Human chr19 + 797502 797502 797502 CGTCCCCCGCGGGTCTGCTCTGTGTGCCATGGACGGGTGAGTCGCACGTCGCCCCGCGCCCCACC CGTCCCCCGCGGGTCTGCTCTGTGTGCCATGGGCGGGTGAGTCGCACGTCGCCCCGCGCCCCACC A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:797451..797874;chr19:797451..797835 26863196 MeRIP-seq:(Medium) rs756429007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4556923,Human_RBP_ID_5144754,Human_RBP_ID_5374581,Human_RBP_ID_8496714,Human_RBP_ID_17670259,Human_RBP_ID_22448078,Human_RBP_ID_23811441 Human_Splice_Rec_1928949,Human_Splice_Rec_1928975,Human_Splice_Rec_1928987,Human_Splice_Rec_1928995,Human_Splice_Rec_1929021,Human_Splice_Rec_1929029,Human_Splice_Rec_1929051,Human_Splice_Rec_1929079,Human_Splice_Rec_1929107,Human_Splice_Rec_1929121 RMVar_hsa_circ_117637,RMVar_hsa_circ_190902 80084 RMVar_ID_80084 Human_SNP_ID_655161617 m1A Human chr19 - 797720 797720 797720 GTGCGCTAGGGACGGGGCGCGCGGGGGCCGGAAGCGGGCCGGACGGGGGATGGGGACGCGGCCAG GTGCGCTAGGGACGGGGCGCGCGGGGGCCGGAGGCGGGCCGGACGGGGGATGGGGACGCGGCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:797715..797858 26863196 MeRIP-seq:(Medium) rs1190315359 Functional Loss SNV dbSNP153 33..33 33 - - - 80085 RMVar_ID_80085 Human_SNP_ID_655161653 m1A Human chr19 - 797770 797770 797770 AAGGCGAAGTGCGGGGACGCGCGCGGAGGGGGAGGGGCGCGGGAGGCCGCGTGCGCTAGGGACGG AAGGCGAAGTGCGGGGACGCGCGCGGAGGGGGGGGGGCGCGGGAGGCCGCGTGCGCTAGGGACGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:797759..798009 26863196 MeRIP-seq:(Medium) rs1409969962 Functional Loss SNV dbSNP153 33..33 33 - - - 80086 RMVar_ID_80086 Human_SNP_ID_655162087 m1A Human chr19 + 798406 798406 798406 ATAGGAAGCGGGAGAGGCTGGAGATGTTTCGCATTCTTTCCGTTTTCCTGAGAAGTTTTTCTTGG ATAGGAAGCGGGAGAGGCTGGAGATGTTTCGCTTTCTTTCCGTTTTCCTGAGAAGTTTTTCTTGG A T PTBP1 Ensembl:ENSG00000011304 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:798402..798497 26863196 MeRIP-seq:(Medium) rs1336795597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52498,Human_RBP_ID_2572406,Human_RBP_ID_3579678,Human_RBP_ID_25438836 RMVar_hsa_circ_117637,RMVar_hsa_circ_190902 80087 RMVar_ID_80087 Human_SNP_ID_655162594 m1A Human chr19 - 799404 799401 799405 CCAACGGCTATATCTGGGACAATGCTGTAGAGAGAAAGAAAGGAGACAACGTTAGCCTGGTGGCC CCAACGGCTATATCTGGGACAATGCTGTAGA____AAGAAAGGAGACAACGTTAGCCTGGTGGCC TTCTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr19:799401..799450;chr19:799401..799475 26863196,26863410,26863410,26863196 MeRIP-seq:(Medium) rs778125417 Functional Loss DEL dbSNP153 32..35 33 - - - 80088 RMVar_ID_80088 Human_SNP_ID_655162595 m1A Human chr19 - 799404 799401 799405 CCAACGGCTATATCTGGGACAATGCTGTAGAGAGAAAGAAAGGAGACAACGTTAGCCTGGTGGCC CCAACGGCTATATCTGGGACAATGCTGTAGA__GAAAGAAAGGAGACAACGTTAGCCTGGTGGCC TTCTC TTC - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr19:799401..799450;chr19:799401..799475 26863196,26863410,26863410,26863196 MeRIP-seq:(Medium) rs778125417 Functional Loss DEL dbSNP153 32..33 33 - - - 80089 RMVar_ID_80089 Human_SNP_ID_655162596 m1A Human chr19 - 799404 799404 799404 CCAACGGCTATATCTGGGACAATGCTGTAGAGAGAAAGAAAGGAGACAACGTTAGCCTGGTGGCC CCAACGGCTATATCTGGGACAATGCTGTAGAGGGAAAGAAAGGAGACAACGTTAGCCTGGTGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr19:799401..799450;chr19:799401..799475 26863196,26863410,26863410,26863196 MeRIP-seq:(Medium) rs1157504890 Functional Loss SNV dbSNP153 33..33 33 - - - 80090 RMVar_ID_80090 Human_SNP_ID_655162699 m1A Human chr19 - 799568 799568 799568 AAACCCTACCGCCCAACTCCAGATTCCAGACCAAGGGTAGTGCCCCTTAGGAATGGAAAAGCGCC AAACCCTACCGCCCAACTCCAGATTCCAGACCGAGGGTAGTGCCCCTTAGGAATGGAAAAGCGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:799565..799667 32194978 MeRIP-seq:(Medium) rs142107622 Functional Loss SNV dbSNP153 33..33 33 - - - 80091 RMVar_ID_80091 Human_SNP_ID_655163048 m1A Human chr19 + 800363 800363 800363 GGTGTGCGAATCTTGCAGCCCCATGGAGGGTGAGGCCAGGGCTCAGCATGTGAGGAAAGGGGGTC GGTGTGCGAATCTTGCAGCCCCATGGAGGGTGCGGCCAGGGCTCAGCATGTGAGGAAAGGGGGTC A C PTBP1 Ensembl:ENSG00000011304 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:800361..800450 26863196 MeRIP-seq:(Medium) rs1470336483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6793865,Human_RBP_ID_13533809,Human_RBP_ID_18421037,Human_RBP_ID_18742157 RMVar_hsa_circ_24441,RMVar_hsa_circ_117637,RMVar_hsa_circ_190902,RMVar_hsa_circ_10537 80092 RMVar_ID_80092 Human_SNP_ID_655164651 m1A Human chr19 - 804087 804087 804087 GGAGCTTCCGGATGTGGATCACTCTAGAGGGGACGCCTGCACTTCGGCTGTCACCTTTGAACTTC GGAGCTTCCGGATGTGGATCACTCTAGAGGGGTCGCCTGCACTTCGGCTGTCACCTTTGAACTTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:804000..804385 26863196 MeRIP-seq:(Medium) rs752171101 Functional Loss SNV dbSNP153 33..33 33 - - - 80093 RMVar_ID_80093 Human_SNP_ID_655164774 m1A Human chr19 + 804331 804331 804331 TCGAGATGAACACGGAGGAGGCTGCCAACACCATGGTGAACTACTACACCTCGGTGACCCCTGTG TCGAGATGAACACGGAGGAGGCTGCCAACACCGTGGTGAACTACTACACCTCGGTGACCCCTGTG A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:804326..804350 26863196 MeRIP-seq:(Medium) rs1476916702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52502,Human_RBP_ID_1574663,Human_RBP_ID_6794145,Human_RBP_ID_9379954,Human_RBP_ID_18442206,Human_RBP_ID_26334988,Human_RBP_ID_26997685,Human_RBP_ID_27157999,Human_RBP_ID_27280351,Human_RBP_ID_27472794 Human_Splice_Rec_1928956,Human_Splice_Rec_1929002,Human_Splice_Rec_1929026,Human_Splice_Rec_1929036,Human_Splice_Rec_1929058,Human_Splice_Rec_1929086,Human_Splice_Rec_1929114,Human_Splice_Rec_1929138 RMVar_hsa_circ_24441,RMVar_hsa_circ_117637,RMVar_hsa_circ_190902,RMVar_hsa_circ_310732,RMVar_hsa_circ_361069,RMVar_hsa_circ_10537,RMVar_hsa_circ_366009,RMVar_hsa_circ_317702,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_96776,RMVar_hsa_circ_75523,RMVar_hsa_circ_190904,RMVar_hsa_circ_190905,RMVar_hsa_circ_372992,RMVar_hsa_circ_44569,RMVar_hsa_circ_68621,RMVar_hsa_circ_119201,RMVar_hsa_circ_190906,RMVar_hsa_circ_190907,RMVar_hsa_circ_190908 80094 RMVar_ID_80094 Human_SNP_ID_655164963 m1A Human chr19 + 804619 804619 804619 TGGCTGCCTCGGCGGCGGCCGTGGACGCAGGGATGGCGATGGCCGGGCAGAGCCCCGTGCTCAGG TGGCTGCCTCGGCGGCGGCCGTGGACGCAGGGGTGGCGATGGCCGGGCAGAGCCCCGTGCTCAGG A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:804539..804701 26863196 MeRIP-seq:(Medium) rs1474168893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529555,Human_RBP_ID_22069340,Human_RBP_ID_22447085,Human_RBP_ID_22533050,Human_RBP_ID_27472798 Human_Splice_Rec_1928957,Human_Splice_Rec_1928994,Human_Splice_Rec_1929004,Human_Splice_Rec_1929005,Human_Splice_Rec_1929028,Human_Splice_Rec_1929038,Human_Splice_Rec_1929039,Human_Splice_Rec_1929060,Human_Splice_Rec_1929061,Human_Splice_Rec_1929088,Human_Splice_Rec_1929089,Human_Splice_Rec_1929116,Human_Splice_Rec_1929117,Human_Splice_Rec_1929140,Human_Splice_Rec_1929141,Human_Splice_Rec_1929161,Human_Splice_Rec_1929172,Human_Splice_Rec_1929173,Human_Splice_Rec_1929187 Human_miRNA_ID_2396162 RMVar_hsa_circ_24441,RMVar_hsa_circ_117637,RMVar_hsa_circ_190902,RMVar_hsa_circ_310732,RMVar_hsa_circ_361069,RMVar_hsa_circ_10537,RMVar_hsa_circ_366009,RMVar_hsa_circ_317702,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_96776,RMVar_hsa_circ_190904,RMVar_hsa_circ_190905,RMVar_hsa_circ_372992,RMVar_hsa_circ_44569,RMVar_hsa_circ_68621,RMVar_hsa_circ_119201,RMVar_hsa_circ_190906,RMVar_hsa_circ_120116,RMVar_hsa_circ_190907,RMVar_hsa_circ_190908,RMVar_hsa_circ_127505,RMVar_hsa_circ_190909,RMVar_hsa_circ_190910 80095 RMVar_ID_80095 Human_SNP_ID_655165175 m1A Human chr19 + 805062 805062 805062 CATCTACAACGCCTGCTGCACGCTGCGCATCGACTTTTCCAAGCTCACCAGCCTCAACGTCAAGT CATCTACAACGCCTGCTGCACGCTGCGCATCGTCTTTTCCAAGCTCACCAGCCTCAACGTCAAGT A T PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:804939..805130 26863196 MeRIP-seq:(Medium) rs774431350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52506,Human_RBP_ID_529560,Human_RBP_ID_1019252,Human_RBP_ID_1574698,Human_RBP_ID_1893708,Human_RBP_ID_8496861,Human_RBP_ID_8838577,Human_RBP_ID_13534659,Human_RBP_ID_17271431,Human_RBP_ID_17502163,Human_RBP_ID_18442210,Human_RBP_ID_18532673,Human_RBP_ID_18742233,Human_RBP_ID_20429396,Human_RBP_ID_22069181,Human_RBP_ID_22241172,Human_RBP_ID_22812979,Human_RBP_ID_26997712,Human_RBP_ID_27280364 Human_Splice_Rec_1928960,Human_Splice_Rec_1929008,Human_Splice_Rec_1929042,Human_Splice_Rec_1929064,Human_Splice_Rec_1929092,Human_Splice_Rec_1929120,Human_Splice_Rec_1929144,Human_Splice_Rec_1929164,Human_Splice_Rec_1929176,Human_Splice_Rec_1929190,Human_Splice_Rec_1929202 Human_miRNA_ID_272484,Human_miRNA_ID_2052640 RMVar_hsa_circ_24441,RMVar_hsa_circ_117637,RMVar_hsa_circ_190902,RMVar_hsa_circ_310732,RMVar_hsa_circ_361069,RMVar_hsa_circ_10537,RMVar_hsa_circ_366009,RMVar_hsa_circ_317702,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_93785,RMVar_hsa_circ_96776,RMVar_hsa_circ_190904,RMVar_hsa_circ_190905,RMVar_hsa_circ_44569,RMVar_hsa_circ_68621,RMVar_hsa_circ_120116,RMVar_hsa_circ_190908,RMVar_hsa_circ_127505,RMVar_hsa_circ_190909,RMVar_hsa_circ_190910,RMVar_hsa_circ_190916,RMVar_hsa_circ_279284,RMVar_hsa_circ_190912,RMVar_hsa_circ_283014,RMVar_hsa_circ_369736,RMVar_hsa_circ_97083,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_89521,RMVar_hsa_circ_190917,RMVar_hsa_circ_190914,RMVar_hsa_circ_190915,RMVar_hsa_circ_190913 80096 RMVar_ID_80096 Human_SNP_ID_655166010 m1A Human chr19 - 806438 806438 806438 CCGCCGCCGCCGAGGGGATGGCCAGGGGGGCCAGGGCGCCGTGGACGTTCGGAACGGAAAGGCCT CCGCCGCCGCCGAGGGGATGGCCAGGGGGGCCTGGGCGCCGTGGACGTTCGGAACGGAAAGGCCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:806425..806616 26863196 MeRIP-seq:(Medium) rs767861441 Functional Loss SNV dbSNP153 33..33 33 - - - 80097 RMVar_ID_80097 Human_SNP_ID_655166089 m1A Human chr19 - 806526 806526 806526 ACCTCTGGGTTGAGGTTGCTGACCAGCAATACAGAATTTCCTGCCCCCGCCAGGCCCGGGATGGC ACCTCTGGGTTGAGGTTGCTGACCAGCAATACGGAATTTCCTGCCCCCGCCAGGCCCGGGATGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:806349..806575;chr19:806373..806598 26863196 MeRIP-seq:(Medium) rs373977560 Functional Loss SNV dbSNP153 33..33 33 - - - 80098 RMVar_ID_80098 Human_SNP_ID_655166944 m1A Human chr19 + 808438 808438 808438 GGAGAACGCCCTAGTGCAGATGGCGGACGGCAACCAGGCCCAGCTGGGTAAGAGGCCGGGGCGGC GGAGAACGCCCTAGTGCAGATGGCGGACGGCAGCCAGGCCCAGCTGGGTAAGAGGCCGGGGCGGC A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:808311..808791 26863196 MeRIP-seq:(Medium) rs202193666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238885,Human_RBP_ID_769808,Human_RBP_ID_5500393,Human_RBP_ID_13535153,Human_RBP_ID_17934011,Human_RBP_ID_18995572,Human_RBP_ID_22446261 Human_Splice_Rec_1928968,Human_Splice_Rec_1928969,Human_Splice_Rec_1928980,Human_Splice_Rec_1928981,Human_Splice_Rec_1929014,Human_Splice_Rec_1929015,Human_Splice_Rec_1929044,Human_Splice_Rec_1929045,Human_Splice_Rec_1929072,Human_Splice_Rec_1929073,Human_Splice_Rec_1929100,Human_Splice_Rec_1929101,Human_Splice_Rec_1929124,Human_Splice_Rec_1929125,Human_Splice_Rec_1929152,Human_Splice_Rec_1929153,Human_Splice_Rec_1929180,Human_Splice_Rec_1929181,Human_Splice_Rec_1929196,Human_Splice_Rec_1929197,Human_Splice_Rec_1929210,Human_Splice_Rec_1929211,Human_Splice_Rec_1929219 RMVar_hsa_circ_24441,RMVar_hsa_circ_361069,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_93785,RMVar_hsa_circ_96776,RMVar_hsa_circ_190908,RMVar_hsa_circ_190912,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_89521,RMVar_hsa_circ_190917,RMVar_hsa_circ_926,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 80099 RMVar_ID_80099 Human_SNP_ID_655168124 m1A Human chr19 + 810783 810783 810783 CCTCATTGACCTGCACAACCACGACCTCGGGGAGAACCACCACCTGCGGGTCTCCTTCTCCAAGT CCTCATTGACCTGCACAACCACGACCTCGGGGGGAACCACCACCTGCGGGTCTCCTTCTCCAAGT A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:810751..810825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_6794295 Human_Splice_Rec_1928974,Human_Splice_Rec_1928986,Human_Splice_Rec_1929020,Human_Splice_Rec_1929050,Human_Splice_Rec_1929078,Human_Splice_Rec_1929106,Human_Splice_Rec_1929158,Human_Splice_Rec_1929186,Human_Splice_Rec_1929216,Human_Splice_Rec_1929224 80100 RMVar_ID_80100 Human_SNP_ID_655168182 m1A Human chr19 + 810877 810877 810877 CCGGGCCCCCTGGCGACAACTTCCATCATTCCAGAGAAAAGCCACTTTAAAAACAGCTGAAGTGA CCGGGCCCCCTGGCGACAACTTCCATCATTCCGGAGAAAAGCCACTTTAAAAACAGCTGAAGTGA A G PTBP1 Ensembl:ENSG00000011304 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:810525..810885 26863196 MeRIP-seq:(Medium) rs754622166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54812,Human_RBP_ID_1019262,Human_RBP_ID_1574764,Human_RBP_ID_1893735,Human_RBP_ID_9293032,Human_RBP_ID_17271443,Human_RBP_ID_17386273,Human_RBP_ID_17502165,Human_RBP_ID_17934016,Human_RBP_ID_18532681,Human_RBP_ID_18742281,Human_RBP_ID_23181274,Human_RBP_ID_26471090,Human_RBP_ID_26814740,Human_RBP_ID_26997790,Human_RBP_ID_27280395 Human_miRNA_ID_935920,Human_miRNA_ID_955910,Human_miRNA_ID_1547194 80101 RMVar_ID_80101 Human_SNP_ID_655168224 m1A Human chr19 - 811025 811000 811025 GAGGGCCGGGAACTCCCGCTGCCACAGTCACCAAGAGCCTGAGCTGTCCCTGTCACCGCAGGGTG GAGGGCCGGGAACTCCCGCTGCCACAGTCACC_________________________GCAGGGTG CGGTGACAGGGACAGCTCAGGCTCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:810976..811275 32194978 MeRIP-seq:(Medium) rs1192737101 Functional Loss DEL dbSNP153 33..57 33 - - - 80102 RMVar_ID_80102 Human_SNP_ID_655168366 m1A Human chr19 + 811238 811238 811238 TGGGGACCCAAGGGGTGGGGGGGTCACACCAGAGAGAGGCAGGGGGCCTGGCCGGCTCCTGCAGG TGGGGACCCAAGGGGTGGGGGGGTCACACCAGGGAGAGGCAGGGGGCCTGGCCGGCTCCTGCAGG A G PTBP1 Ensembl:ENSG00000011304 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1378739498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54815,Human_RBP_ID_529591,Human_RBP_ID_5191972,Human_RBP_ID_25439176,Human_RBP_ID_26471473,Human_RBP_ID_26997798 Human_miRNA_ID_935922,Human_miRNA_ID_955912 80103 RMVar_ID_80103 Human_SNP_ID_655168397 m1A Human chr19 - 811301 811289 811301 ACTTGATTAGAGGGCTGGGGTTGGGGTGTCGCAGCCGCGGCCGCCGCGCCCCAGCTGCATGATCC ACTTGATTAGAGGGCTGGGGTTGGGGTGTCGC____________CGCGCCCCAGCTGCATGATCC GGCGGCCGCGGCT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:811026..811350 26863410 MeRIP-seq:(Medium) rs1249541170 Functional Loss DEL dbSNP153 33..44 33 - - - 80104 RMVar_ID_80104 Human_SNP_ID_655168405 m1A Human chr19 - 811301 811292 811301 ACTTGATTAGAGGGCTGGGGTTGGGGTGTCGCAGCCGCGGCCGCCGCGCCCCAGCTGCATGATCC ACTTGATTAGAGGGCTGGGGTTGGGGTGTCGC_________CGCCGCGCCCCAGCTGCATGATCC GGCCGCGGCT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:811026..811350 26863410 MeRIP-seq:(Medium) rs1331975383 Functional Loss DEL dbSNP153 33..41 33 - - - 80105 RMVar_ID_80105 Human_SNP_ID_655168497 m1A Human chr19 - 811391 811391 811391 TGTCGACCAGCTCCGCAGCTGGAGCAGCGGGGAGCCCGCCTGGGGGCAGAAGGGAAGGCCCTGGG TGTCGACCAGCTCCGCAGCTGGAGCAGCGGGGGGCCCGCCTGGGGGCAGAAGGGAAGGCCCTGGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:811229..811500 32194978 MeRIP-seq:(Medium) rs1041467388 Functional Loss SNV dbSNP153 33..33 33 - - - 80106 RMVar_ID_80106 Human_SNP_ID_655168974 m1A Human chr19 - 812169 812169 812169 ATCGGTTCTCTCCGCGTCACAAGCCATCGGGTAAGGCAACGGAATGTGCGTGGGGTCCCCTGTGG ATCGGTTCTCTCCGCGTCACAAGCCATCGGGTCAGGCAACGGAATGTGCGTGGGGTCCCCTGTGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:812027..812250 32194978 MeRIP-seq:(Medium) rs1176765940 Functional Loss SNV dbSNP153 33..33 33 - - - 80107 RMVar_ID_80107 Human_SNP_ID_655170066 m1A Human chr19 + 813769 813769 813769 CCCTGGGGGCCCCAGCTCGTCGGTGCTCACCGACTTATTCTGCTGATAAACCGAGTCGTGGCCCC CCCTGGGGGCCCCAGCTCGTCGGTGCTCACCGCCTTATTCTGCTGATAAACCGAGTCGTGGCCCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:813732..813833 32194978 MeRIP-seq:(Medium) rs1477403728 Functional Loss SNV dbSNP153 33..33 33 - - - 80108 RMVar_ID_80108 Human_SNP_ID_655171427 m1A Human chr19 + 816571 816571 816571 GTGGTACCCATCCATCCATCCATCCATTCATCACCCAGCCATTCATTCATCTATCCATCCATCCA GTGGTACCCATCCATCCATCCATCCATTCATCCCCCAGCCATTCATTCATCTATCCATCCATCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:816559..816815 26863196 MeRIP-seq:(Medium) rs991228255 Functional Loss SNV dbSNP153 33..33 33 - - - 80109 RMVar_ID_80109 Human_SNP_ID_655175979 m1A Human chr19 + 828776 828776 828776 AGGGGCTCAGATGGAGGAGGTGCAGAGAAGGGAAGGGGGTCAGATGGGGGAGGCCCAGAGAAGGG AGGGGCTCAGATGGAGGAGGTGCAGAGAAGGGGAGGGGGTCAGATGGGGGAGGCCCAGAGAAGGG A G AZU1 Ensembl:ENSG00000172232 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:828774..828911 26863196 MeRIP-seq:(Medium) rs1368324714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39295 80110 RMVar_ID_80110 Human_SNP_ID_655176222 m1A Human chr19 - 829278 829278 829278 GTCCCTTCCCTTCTCTGAGCCTCCTCCATCTGACCCCCTCCCCTTCTCTGCACCTCCTCCATCTG GTCCCTTCCCTTCTCTGAGCCTCCTCCATCTGCCCCCCTCCCCTTCTCTGCACCTCCTCCATCTG T G HSALNG0122936 RNACentral:URS0000EA9395 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:828988..829580 26863196 MeRIP-seq:(Medium) rs1389925639 Functional Loss SNV dbSNP153 33..33 33 - - - 80111 RMVar_ID_80111 Human_SNP_ID_655177254 m1A Human chr19 - 831816 831815 831816 GAACACCATCGATCCAGTCTCGGAAGAGCGCCACTCGGGTGAAGAAGTCAGGGCCTCGGCCACAG GAACACCATCGATCCAGTCTCGGAAGAGCGCC_CTCGGGTGAAGAAGTCAGGGCCTCGGCCACAG GT G lnc-PLPPR3-3 RNACentral:URS00008BB1F6 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:831770..831869 32194978 MeRIP-seq:(Medium) rs372854624 Functional Loss DEL dbSNP153,HGVD 33..33 33 - - - 80112 RMVar_ID_80112 Human_SNP_ID_655179753 m1A Human chr19 + 836302 836302 836302 CGGACAGAGACACAGAGACAGAGAGAGACGGAAAAAGAGGGACAGAGCCAGAGAGACTGAGAGAG CGGACAGAGACACAGAGACAGAGAGAGACGGAGAAAGAGGGACAGAGCCAGAGAGACTGAGAGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:836291..836384 26863196 MeRIP-seq:(Medium) rs1166193905 Functional Loss SNV dbSNP153 33..33 33 - - - 80113 RMVar_ID_80113 Human_SNP_ID_655185444 m1A Human chr19 - 851482 851377 851482 GCCCCGTGATACCGGCCACATGCAGCTGTGTCACCTGCCTCAGTTTACCCAGGGCCCTGTGATAC GCCCCGTGATACCGGCCACATGCAGCTGTGTC_________________________________ CGACACAGCTGCATGTGGCCGGTATCACAGGGCCCTGGGTAAACTGAGGCAGGCGACACAGCTGCATGTGGCCGTATCACAGGGCCCTGGGTAAACTGAGGCAGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:851465..851536 26863196 MeRIP-seq:(Medium) rs1568303022 Functional Loss DEL dbSNP153 33..65 33 - - - 80114 RMVar_ID_80114 Human_SNP_ID_655185479 m1A Human chr19 - 851482 851482 851482 GCCCCGTGATACCGGCCACATGCAGCTGTGTCACCTGCCTCAGTTTACCCAGGGCCCTGTGATAC GCCCCGTGATACCGGCCACATGCAGCTGTGTCGCCTGCCTCAGTTTACCCAGGGCCCTGTGATAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:851465..851536 26863196 MeRIP-seq:(Medium) rs1373463131 Functional Loss SNV dbSNP153 33..33 33 - - - 80115 RMVar_ID_80115 Human_SNP_ID_655189971 m1A Human chr19 - 861972 861972 861972 TCCCGGGGCCTGCAGGCCCCGCGTCTCCTCCCAGGCCTGAAGGCTCACCTTGCAGCTGTCCCGGC TCCCGGGGCCTGCAGGCCCCGCGTCTCCTCCCGGGCCTGAAGGCTCACCTTGCAGCTGTCCCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:861969..862066 26863196 MeRIP-seq:(Medium) rs1432656107 Functional Loss SNV dbSNP153 33..33 33 - - - 80116 RMVar_ID_80116 Human_SNP_ID_655189989 m1A Human chr19 + 861994 861986 861994 CCTTCAGGCCTGGGAGGAGACGCGGGGCCTGCAGGCCCCGGGAAGGGCCTGCAGAGGGAGCGCGA CCTTCAGGCCTGGGAGGAGACGCGG________GGCCCCGGGAAGGGCCTGCAGAGGGAGCGCGA GGGCCTGCA G CFD Ensembl:ENSG00000197766 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:861983..862070 26863196 MeRIP-seq:(Medium) rs1306988470 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_55622,Human_RBP_ID_3579708,Human_RBP_ID_21978291,Human_RBP_ID_22476789 80117 RMVar_ID_80117 Human_SNP_ID_655190731 m1A Human chr19 - 863295 863295 863295 CAATAAAGACCAACCAGATGCAGGAGTGGATGACTTCATTGCTCGGGACTTTGTTGCTTGGGTGA CAATAAAGACCAACCAGATGCAGGAGTGGATGGCTTCATTGCTCGGGACTTTGTTGCTTGGGTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:863245..863501 26863196 MeRIP-seq:(Medium) rs943735680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2572684,Human_RBP_ID_3579165,Human_RBP_ID_5500409,Human_RBP_ID_13537976 80118 RMVar_ID_80118 Human_SNP_ID_655190755 m1A Human chr19 + 863368 863368 863368 CTATATGCAGAAGGGGAGGCCGAGGTGGGAGGATCATTGGATCTCAGGAGTTCGAGATCAGCATG CTATATGCAGAAGGGGAGGCCGAGGTGGGAGGTTCATTGGATCTCAGGAGTTCGAGATCAGCATG A T CFD Ensembl:ENSG00000197766 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:863317..863509 26863196 MeRIP-seq:(Medium) rs958612071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8497125 80119 RMVar_ID_80119 Human_SNP_ID_655192222 m1A Human chr19 - 865870 865869 865871 CCTCCGTAGCTCCTGCGGACCAAAGGATGCAAAGATGCCCAGGCAGGCCGGATGCAGCAGCTCAC CCTCCGTAGCTCCTGCGGACCAAAGGATGCA__GATGCCCAGGCAGGCCGGATGCAGCAGCTCAC CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:865860..866036 26863196 MeRIP-seq:(Medium) rs1044421191 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13538041 80120 RMVar_ID_80120 Human_SNP_ID_655192603 m1A Human chr19 - 866579 866538 866580 GTGCAGGCCCGCGGCGGGTGGACGGGGAGGAGATGGGAGCGCTGGCGAGGGGTGCAGGCCTGCGG GTGCAGGCCCGCGGCGGGTGGACGGGGAGGA__________________________________ GTCCACCCGCCGCAGGCCTGCACCCCTCGCCAGCGCTCCCATC G lnc-MED16-1 RNACentral:URS00008C2ED3 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:866447..866650;chr19:866324..866650 26863196 MeRIP-seq:(Medium) rs1568313789 Functional Loss DEL dbSNP153 32..65 33 - - - 80121 RMVar_ID_80121 Human_SNP_ID_655192710 m1A Human chr19 - 866717 866701 866717 GGGTGGACGGGGAGGAGATGGGAGCGCTGGCGAGGGGTGCAGGCCCGCGGCGGGTGGACGGGGAG GGGTGGACGGGGAGGAGATGGGAGCGCTGGCG________________GGCGGGTGGACGGGGAG CGCGGGCCTGCACCCCT C lnc-MED16-1,lnc-MED16-1:2 RNACentral:URS00008C2ED3,RNACentral:URS00008C347E lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:866526..866946 26863196 MeRIP-seq:(Medium) rs1346828126 Functional Loss DEL dbSNP153 33..48 33 - - - 80122 RMVar_ID_80122 Human_SNP_ID_655193038 m1A Human chr19 + 867184 867184 867184 CCCACACACTCCTGAGCTCGAGAGGAGGTCGCAGGAGTGGGGCCGGGAGCTGCCCTAGGGTCTGT CCCACACACTCCTGAGCTCGAGAGGAGGTCGCTGGAGTGGGGCCGGGAGCTGCCCTAGGGTCTGT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:867145..867262 26863196 MeRIP-seq:(Medium) rs1012659119 Functional Loss SNV dbSNP153 33..33 33 - - - 80123 RMVar_ID_80123 Human_SNP_ID_655193187 m1A Human chr19 + 867442 867442 867442 CCCTCGCTGCCCTCCCCAGAGCTGCAGAAAGGAGGAGTCCGTCGGCACACAGCAGGGGCACCACT CCCTCGCTGCCCTCCCCAGAGCTGCAGAAAGGGGGAGTCCGTCGGCACACAGCAGGGGCACCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:867433..867751 26863196 MeRIP-seq:(Medium) rs1204254266 Functional Loss SNV dbSNP153 33..33 33 - - - 80124 RMVar_ID_80124 Human_SNP_ID_655193188 m1A Human chr19 + 867442 867442 867442 CCCTCGCTGCCCTCCCCAGAGCTGCAGAAAGGAGGAGTCCGTCGGCACACAGCAGGGGCACCACT CCCTCGCTGCCCTCCCCAGAGCTGCAGAAAGGTGGAGTCCGTCGGCACACAGCAGGGGCACCACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:867433..867751 26863196 MeRIP-seq:(Medium) rs1204254266 Functional Loss SNV dbSNP153 33..33 33 - - - 80125 RMVar_ID_80125 Human_SNP_ID_655193280 m1A Human chr19 + 867627 867607 867628 GGGACAGAGTCAGGCAGAGACACAGAAACAGCATGCAGAGACACAGAGACCATACACAGAGAAGT GGGACAGAGTCAG_____________________GCAGAGACACAGAGACCATACACAGAGAAGT GGCAGAGACACAGAAACAGCAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:867373..867801 26863196 MeRIP-seq:(Medium) rs575915108 Functional Loss DEL dbSNP153 14..34 33 - - - 80126 RMVar_ID_80126 Human_SNP_ID_655193318 m1A Human chr19 + 867654 867654 867654 ACAGCATGCAGAGACACAGAGACCATACACAGAGAAGTGCAGAGATACCAGAGACACGCAGAAAC ACAGCATGCAGAGACACAGAGACCATACACAGCGAAGTGCAGAGATACCAGAGACACGCAGAAAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:867421..868443 26863196 MeRIP-seq:(Medium) rs1015155115 Functional Loss SNV dbSNP153 33..33 33 - - - 80127 RMVar_ID_80127 Human_SNP_ID_655193780 m1A Human chr19 + 868351 868340 868351 CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGAGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC CGGGCTCAGGGGCAGCTGAGGG___________GTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC GGTAGCTGAGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868210..868452 26863196 MeRIP-seq:(Medium) rs3217342 Functional Loss DEL dbSNP153 23..33 33 - - - 80128 RMVar_ID_80128 Human_SNP_ID_655193792 m1A Human chr19 + 868351 868351 868351 CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGAGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGGGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868210..868452 26863196 MeRIP-seq:(Medium) rs981655742 Functional Loss SNV dbSNP153 33..33 33 - - - 80129 RMVar_ID_80129 Human_SNP_ID_655194177 m1A Human chr19 - 868930 868930 868930 TCCCCTCTCCCGCCAGGGCCCCAGGCCAGCCCAAGATCGACCACCTGCGGAGGCTGCACCTTGGC TCCCCTCTCCCGCCAGGGCCCCAGGCCAGCCCGAGATCGACCACCTGCGGAGGCTGCACCTTGGC T C MED16 Ensembl:ENSG00000175221 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868923..869272 26863196 MeRIP-seq:(Medium) rs754553007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22661422 Human_Splice_Rec_1929348,Human_Splice_Rec_1929349,Human_Splice_Rec_1929376,Human_Splice_Rec_1929377,Human_Splice_Rec_1929380,Human_Splice_Rec_1929381,Human_Splice_Rec_1929400,Human_Splice_Rec_1929401,Human_Splice_Rec_1929428,Human_Splice_Rec_1929429,Human_Splice_Rec_1929441,Human_Splice_Rec_1929470,Human_Splice_Rec_1929471 RMVar_hsa_circ_94288,RMVar_hsa_circ_78081,RMVar_hsa_circ_190922,RMVar_hsa_circ_190923 80130 RMVar_ID_80130 Human_SNP_ID_655198770 m1A Human chr19 - 875349 875349 875349 GCGACTACCACACCAAGCTCTTCCTCATCGCCATCAGCTCCACCCTGAAGTCGCTGCTGCGCCCC GCGACTACCACACCAAGCTCTTCCTCATCGCCGTCAGCTCCACCCTGAAGTCGCTGCTGCGCCCC T C MED16 Ensembl:ENSG00000175221 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:875299..875413 26863196 MeRIP-seq:(Medium) rs777296856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27839060 RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 80131 RMVar_ID_80131 Human_SNP_ID_655200381 m1A Human chr19 + 877792 877792 877792 TGCCCACCAGCCCCAGCCCCAGCCCCAGCCCCAGCCCCACGTGCCCCAGCAGCTCGCCTTCCCGT TGCCCACCAGCCCCAGCCCCAGCCCCAGCCCCTGCCCCACGTGCCCCAGCAGCTCGCCTTCCCGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:877785..877879 26863196 MeRIP-seq:(Medium) rs1228638517 Functional Loss SNV dbSNP153 33..33 33 - - - 80132 RMVar_ID_80132 Human_SNP_ID_655200409 m1A Human chr19 + 877839 877839 877839 AGCAGCTCGCCTTCCCGTGGTTGTCAATGCCCACCAAGCCCAGCCCCACATGCCCCAGCAGCTCG AGCAGCTCGCCTTCCCGTGGTTGTCAATGCCCCCCAAGCCCAGCCCCACATGCCCCAGCAGCTCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:877464..877879 26863196 MeRIP-seq:(Medium) rs1213358183 Functional Loss SNV dbSNP153 33..33 33 - - - 80133 RMVar_ID_80133 Human_SNP_ID_655200461 m1A Human chr19 + 878022 877949 878023 AGCTCACCTTTCCGTGGTTGTCAACGCCCACCAGCCCCAGCCCCAGCCCCACGTGCCCCAGCAGC __________________________________CCCCAGCCCCAGCCCCACGTGCCCCAGCAGC CCACCAGCCCCAGCCCCAGCCCCAGCCCCACGTGCCCCAGCAGCTCACCTTTCCGTGGTTGTCAACGCCCACCAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:878020..878197 26863196 MeRIP-seq:(Medium) rs1568325912 Functional Loss DEL dbSNP153 1..34 33 - - - 80134 RMVar_ID_80134 Human_SNP_ID_655200510 m1A Human chr19 + 878022 878017 878023 AGCTCACCTTTCCGTGGTTGTCAACGCCCACCAGCCCCAGCCCCAGCCCCACGTGCCCCAGCAGC AGCTCACCTTTCCGTGGTTGTCAACGCC______CCCCAGCCCCAGCCCCACGTGCCCCAGCAGC CCACCAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:878020..878197 26863196 MeRIP-seq:(Medium) rs1251926279 Functional Loss DEL dbSNP153 29..34 33 - - - 80135 RMVar_ID_80135 Human_SNP_ID_655200565 m1A Human chr19 + 878084 878084 878084 AGCTCGCCTTCCCCTGGCTGTCAATGCCCCCCAGCCCCAGCCCCAGCGCCACGTGCCCCAGCAAC AGCTCGCCTTCCCCTGGCTGTCAATGCCCCCCGGCCCCAGCCCCAGCGCCACGTGCCCCAGCAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:877986..878282 26863196 MeRIP-seq:(Medium) rs1256602599 Functional Loss SNV dbSNP153 33..33 33 - - - 80136 RMVar_ID_80136 Human_SNP_ID_655200612 m1A Human chr19 - 878163 878163 878163 GCACGTGGGGCTGGGCTCGGTGGGCATTGACAACCACGGGAAGGTGAGCTGCTGAGCATTGACAA GCACGTGGGGCTGGGCTCGGTGGGCATTGACAGCCACGGGAAGGTGAGCTGCTGAGCATTGACAA T C MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:877986..878208 26863196 MeRIP-seq:(Medium) rs1229176208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3584352,Human_RBP_ID_5320688,Human_RBP_ID_5369519,Human_RBP_ID_8098959,Human_RBP_ID_8233705,Human_RBP_ID_9425526,Human_RBP_ID_21979524,Human_RBP_ID_22477323,Human_RBP_ID_22698926 RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 80137 RMVar_ID_80137 Human_SNP_ID_655201025 m1A Human chr19 + 878958 878951 878958 CCGGCCCCGGCCCCGGCCCCGGCCGCAGCTCCACGTGCCCCAGCAGCTCACCTTCCCCTGGCTAT CCGGCCCCGGCCCCGGCCCCGGCCGC_______CGTGCCCCAGCAGCTCACCTTCCCCTGGCTAT CAGCTCCA C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:878910..879045 26863196 MeRIP-seq:(Medium) rs1218360121 Functional Loss DEL dbSNP153 27..33 33 - - - 80138 RMVar_ID_80138 Human_SNP_ID_655201026 m1A Human chr19 + 878952 878952 878952 CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCAGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCCGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT A C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:878919..879075 26863196 MeRIP-seq:(Medium) rs1276880691 Functional Loss SNV dbSNP153 33..33 33 - - - 80139 RMVar_ID_80139 Human_SNP_ID_655201027 m1A Human chr19 + 878952 878952 878952 CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCAGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCGGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT A G lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:878919..879075 26863196 MeRIP-seq:(Medium) rs1276880691 Functional Loss SNV dbSNP153 33..33 33 - - - 80140 RMVar_ID_80140 Human_SNP_ID_655201028 m1A Human chr19 + 878952 878952 878952 CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCAGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT CCGGCCCCGGCCCCGGCCCCGGCCCCGGCCGCTGCTCCACGTGCCCCAGCAGCTCACCTTCCCCT A T lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:878919..879075 26863196 MeRIP-seq:(Medium) rs1276880691 Functional Loss SNV dbSNP153 33..33 33 - - - 80141 RMVar_ID_80141 Human_SNP_ID_655201045 m1A Human chr19 - 878984 878984 878984 GCTGGGGCTGGGGCTGGTGGGCATTGATAGCCAGGGGAAGGTGAGCTGCTGGGGCACGTGGAGCT GCTGGGGCTGGGGCTGGTGGGCATTGATAGCCGGGGGAAGGTGAGCTGCTGGGGCACGTGGAGCT T C MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:878902..879093 26863196 MeRIP-seq:(Medium) rs1192738196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262964,Human_RBP_ID_772126,Human_RBP_ID_826074,Human_RBP_ID_1067335,Human_RBP_ID_2572720,Human_RBP_ID_3579729,Human_RBP_ID_5144763,Human_RBP_ID_5238191,Human_RBP_ID_5319691,Human_RBP_ID_5469407,Human_RBP_ID_8098962,Human_RBP_ID_8194859,Human_RBP_ID_8232903,Human_RBP_ID_8728145,Human_RBP_ID_8942268,Human_RBP_ID_9327951,Human_RBP_ID_9425018,Human_RBP_ID_17190793,Human_RBP_ID_17207541,Human_RBP_ID_18191531,Human_RBP_ID_18420801,Human_RBP_ID_18944457,Human_RBP_ID_21977316,Human_RBP_ID_22416532,Human_RBP_ID_22476312,Human_RBP_ID_22524375,Human_RBP_ID_22664204,Human_RBP_ID_22698930,Human_RBP_ID_22718097,Human_RBP_ID_22741351,Human_RBP_ID_23119100,Human_RBP_ID_23278963,Human_RBP_ID_24420015,Human_RBP_ID_26784534 RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 80142 RMVar_ID_80142 Human_SNP_ID_655201062 m1A Human chr19 + 879014 879011 879014 CCTGGCTATCAATGCCCACCAGCCCCAGCCCCAGCCCCACATGTCCCAGCAGCTCACCTTCCCCC CCTGGCTATCAATGCCCACCAGCCCCAGCC___GCCCCACATGTCCCAGCAGCTCACCTTCCCCC CCCA C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:878898..879077 26863196 MeRIP-seq:(Medium) rs1287529181 Functional Loss DEL dbSNP153 31..33 33 - - - 80143 RMVar_ID_80143 Human_SNP_ID_655201063 m1A Human chr19 + 879014 879014 879014 CCTGGCTATCAATGCCCACCAGCCCCAGCCCCAGCCCCACATGTCCCAGCAGCTCACCTTCCCCC CCTGGCTATCAATGCCCACCAGCCCCAGCCCCCGCCCCACATGTCCCAGCAGCTCACCTTCCCCC A C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:878898..879077 26863196 MeRIP-seq:(Medium) rs1335560125 Functional Loss SNV dbSNP153 33..33 33 - - - 80144 RMVar_ID_80144 Human_SNP_ID_655201223 m1A Human chr19 + 879315 879284 879316 GCTCACCTTCCCATGGTTGTCAATGCCCACCAAGCCCAGCCCCACGTGCCCCAGCAGCTCACCTT GC________________________________CCCAGCCCCACGTGCCCCAGCAGCTCACCTT CTCACCTTCCCATGGTTGTCAATGCCCACCAAG C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:879176..879437 26863196 MeRIP-seq:(Medium) rs1489489401 Functional Loss DEL dbSNP153 3..34 33 - - - 80145 RMVar_ID_80145 Human_SNP_ID_655201237 m1A Human chr19 + 879314 879313 879314 AGCTCACCTTCCCATGGTTGTCAATGCCCACCAAGCCCAGCCCCACGTGCCCCAGCAGCTCACCT AGCTCACCTTCCCATGGTTGTCAATGCCCACC_AGCCCAGCCCCACGTGCCCCAGCAGCTCACCT CA C lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:879170..879612;chr19:879172..879454 26863196 MeRIP-seq:(Medium) rs1363274520 Functional Loss DEL dbSNP153 33..33 33 - - - 80146 RMVar_ID_80146 Human_SNP_ID_655201238 m1A Human chr19 + 879315 879315 879315 GCTCACCTTCCCATGGTTGTCAATGCCCACCAAGCCCAGCCCCACGTGCCCCAGCAGCTCACCTT GCTCACCTTCCCATGGTTGTCAATGCCCACCAGGCCCAGCCCCACGTGCCCCAGCAGCTCACCTT A G lnc-CFD-1 RNACentral:URS00008C1A6C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:879176..879437 26863196 MeRIP-seq:(Medium) rs1401431065 Functional Loss SNV dbSNP153 33..33 33 - - - 80147 RMVar_ID_80147 Human_SNP_ID_655201344 m1A Human chr19 - 879520 879520 879520 CTGGGGCGTGGCCCTGGTAGGCATTGACAACCAGGGAAAGGCGAGCTGCTGGGGCACGTGGGGCT CTGGGGCGTGGCCCTGGTAGGCATTGACAACCCGGGAAAGGCGAGCTGCTGGGGCACGTGGGGCT T G MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:879507..879609 26863196 MeRIP-seq:(Medium) rs1228373327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 80148 RMVar_ID_80148 Human_SNP_ID_655201435 m1A Human chr19 - 879659 879659 879659 GCACGTGGGGCTGGGGCTGGTGGGCATTGACAACCAGGGGAACGTGAGCTGCTGGGGCACGTGGG GCACGTGGGGCTGGGGCTGGTGGGCATTGACAGCCAGGGGAACGTGAGCTGCTGGGGCACGTGGG T C MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:879656..879808 26863196 MeRIP-seq:(Medium) rs28414042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5320694 RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 80149 RMVar_ID_80149 Human_SNP_ID_655206162 m1A Human chr19 - 889064 889064 889064 AGGGTTGGGGACAGTTAAGAGTAGGCGTGGCCAGGGTTGGGGGGGACAGTTAAGAGTAGGCGTGG AGGGTTGGGGACAGTTAAGAGTAGGCGTGGCCGGGGTTGGGGGGGACAGTTAAGAGTAGGCGTGG T C MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:889063..889165 26863196 MeRIP-seq:(Medium) rs1221297902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5370827 RMVar_hsa_circ_330639,RMVar_hsa_circ_35642 80150 RMVar_ID_80150 Human_SNP_ID_655206165 m1A Human chr19 + 889075 889072 889075 CTTAACTGTCCCCCCCAACCCTGGCCACGCCTACTCTTAACTGTCCCCAACCCTGGCCACGCCTA CTTAACTGTCCCCCCCAACCCTGGCCACGC___CTCTTAACTGTCCCCAACCCTGGCCACGCCTA CCTA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:889065..889154 26863196 MeRIP-seq:(Medium) rs1429368452 Functional Loss DEL dbSNP153 31..33 33 - - - 80151 RMVar_ID_80151 Human_SNP_ID_655206741 m1A Human chr19 + 890196 890196 890196 TGGCCTCGTGGTGCTCTGAGGGGATCGAGTGCAGGTCCCAGGGGTGCTCCGTGTCCAGGATGTGG TGGCCTCGTGGTGCTCTGAGGGGATCGAGTGCGGGTCCCAGGGGTGCTCCGTGTCCAGGATGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:890187..890256 26863196 MeRIP-seq:(Medium) rs1398312956 Functional Loss SNV dbSNP153 33..33 33 - - - 80152 RMVar_ID_80152 Human_SNP_ID_655207217 m1A Human chr19 + 891122 891122 891122 GTCCATCATCCCACCTGCCGCTGGCCGCCGCAAATCACACATGAGGGCAGTCACCAGCTCCTGCG GTCCATCATCCCACCTGCCGCTGGCCGCCGCATATCACACATGAGGGCAGTCACCAGCTCCTGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:891088..891160 26863196 MeRIP-seq:(Medium) rs750947718 Functional Loss SNV dbSNP153 33..33 33 - - - 80153 RMVar_ID_80153 Human_SNP_ID_655207686 m1A Human chr19 - 891982 891982 891982 TGTTCCCCGTCACACTCAGCCCCGCCTCGGCCACAGGTGTTCCCCGTCACACTCAGCCCCCGGCT TGTTCCCCGTCACACTCAGCCCCGCCTCGGCCCCAGGTGTTCCCCGTCACACTCAGCCCCCGGCT T G MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:891980..892497 26863196 MeRIP-seq:(Medium) rs1466398498 Functional Loss SNV dbSNP153 33..33 33 - - - 80154 RMVar_ID_80154 Human_SNP_ID_655207844 m1A Human chr19 + 892383 892383 892383 AATTCTCAGGCTTCACCGTAGGGGTCCCATGTACTCTCCAGGTCCAGCCTCCAACGCCCTTAGCT AATTCTCAGGCTTCACCGTAGGGGTCCCATGTGCTCTCCAGGTCCAGCCTCCAACGCCCTTAGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:892378..892480 26863196 MeRIP-seq:(Medium) rs1004384422 Functional Loss SNV dbSNP153 33..33 33 - - - 80155 RMVar_ID_80155 Human_SNP_ID_655207927 m1A Human chr19 + 892612 892612 892612 TCCCAGGGACCCCCTACCCTCTCCAGACCCCTATAACTCCGCAGTCCCCAGTCTCCACCCTAGGG TCCCAGGGACCCCCTACCCTCTCCAGACCCCTGTAACTCCGCAGTCCCCAGTCTCCACCCTAGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:892600..892828 26863196 MeRIP-seq:(Medium) rs902740980 Functional Loss SNV dbSNP153 33..33 33 - - - 80156 RMVar_ID_80156 Human_SNP_ID_655207944 m1A Human chr19 + 892684 892655 892685 TCCCTCTCCAGGCCCCGCACCGATAACCCCGCAGTCTCCAGGCCCTGCCTCTACAGCCCCCCAGT TCCC______________________________TCTCCAGGCCCTGCCTCTACAGCCCCCCAGT CTCTCCAGGCCCCGCACCGATAACCCCGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:892653..892965 26863196 MeRIP-seq:(Medium) rs72298146 Functional Loss DEL dbSNP153 5..34 33 - - - 80157 RMVar_ID_80157 Human_SNP_ID_655208249 m1A Human chr19 - 893133 893133 893133 AAGATGGCGGCGCCAGACCCGAGGCGCTAGGGAAGATCGCACCGCGGACGCCCGCTGAGCTTGGC AAGATGGCGGCGCCAGACCCGAGGCGCTAGGGCAGATCGCACCGCGGACGCCCGCTGAGCTTGGC T G MED16 Ensembl:ENSG00000175221 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:893041..893159;chr19:893057..893160;chr19:892999..893136 26863196 MeRIP-seq:(Medium) rs1281241914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774071,Human_RBP_ID_4555906 Human_Splice_Rec_1929323,Human_Splice_Rec_1929351,Human_Splice_Rec_1929403,Human_Splice_Rec_1929433,Human_Splice_Rec_1929443,Human_Splice_Rec_1929519 80158 RMVar_ID_80158 Human_SNP_ID_655208253 m1A Human chr19 + 893138 893138 893138 GCTCAGCGGGCGTCCGCGGTGCGATCTTCCCTAGCGCCTCGGGTCTGGCGCCGCCATCTTCCTCG GCTCAGCGGGCGTCCGCGGTGCGATCTTCCCTGGCGCCTCGGGTCTGGCGCCGCCATCTTCCTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:893041..893154 26863196 MeRIP-seq:(Medium) rs1037204054 Functional Loss SNV dbSNP153 33..33 33 - - - 80159 RMVar_ID_80159 Human_SNP_ID_655211235 m1A Human chr19 + 900783 900783 900783 TCCCGGCCCCACCCACCCCAGGCCACGCCCCCATCCATACCCTGGCCCCACCCATACCCGCCCCA TCCCGGCCCCACCCACCCCAGGCCACGCCCCCCTCCATACCCTGGCCCCACCCATACCCGCCCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:900781..900989 26863196 MeRIP-seq:(Medium) rs558422106 Functional Loss SNV dbSNP153 33..33 33 - - - 80160 RMVar_ID_80160 Human_SNP_ID_655211801 m1A Human chr19 + 902038 902038 902038 CCTTGGCCTTGGGCACGAGGTCTGAGTTCCGCACTGCCTGGTTGATGAAGTGCTGTTTCCGCCTG CCTTGGCCTTGGGCACGAGGTCTGAGTTCCGCCCTGCCTGGTTGATGAAGTGCTGTTTCCGCCTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:902026..902100 26863196 MeRIP-seq:(Medium) rs1251151983 Functional Loss SNV dbSNP153 33..33 33 - - - 80161 RMVar_ID_80161 Human_SNP_ID_655211802 m1A Human chr19 + 902038 902038 902038 CCTTGGCCTTGGGCACGAGGTCTGAGTTCCGCACTGCCTGGTTGATGAAGTGCTGTTTCCGCCTG CCTTGGCCTTGGGCACGAGGTCTGAGTTCCGCGCTGCCTGGTTGATGAAGTGCTGTTTCCGCCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:902026..902100 26863196 MeRIP-seq:(Medium) rs1251151983 Functional Loss SNV dbSNP153 33..33 33 - - - 80162 RMVar_ID_80162 Human_SNP_ID_655211819 m1A Human chr19 + 902073 902073 902073 GCCTGGTTGATGAAGTGCTGTTTCCGCCTGGAAGCCGAGAGTCTCTTCACCTGGGAGCTGGCTAG GCCTGGTTGATGAAGTGCTGTTTCCGCCTGGAGGCCGAGAGTCTCTTCACCTGGGAGCTGGCTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:902026..902182 26863196 MeRIP-seq:(Medium) rs1390123262 Functional Loss SNV dbSNP153 33..33 33 - - - 80163 RMVar_ID_80163 Human_SNP_ID_655211905 m1A Human chr19 - 902317 902317 902317 GCATGAGCCACCACACCCAGCCCGTCTTCACAATTGTATCTGCTTCCTGTGATGTGAGGATGAAA GCATGAGCCACCACACCCAGCCCGTCTTCACAGTTGTATCTGCTTCCTGTGATGTGAGGATGAAA T C R3HDM4 Ensembl:ENSG00000198858 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:902307..913097 32194978 MeRIP-seq:(Medium) rs903915887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17934216 Human_Splice_Rec_1929567 80164 RMVar_ID_80164 Human_SNP_ID_655215239 m1A Human chr19 + 912382 912362 912382 GTTGGGGGGCGGGCCCGGGAGTGGGGGCGCGGACCCGGGAGTGGGGGCGAAGACCAGAGAGTAGG GTTGGGGGGCGGG____________________CCCGGGAGTGGGGGCGAAGACCAGAGAGTAGG GCCCGGGAGTGGGGGCGCGGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:912376..912729 26863196 MeRIP-seq:(Medium) rs1568344798 Functional Loss DEL dbSNP153 14..33 33 - - - 80165 RMVar_ID_80165 Human_SNP_ID_655215246 m1A Human chr19 + 912369 912369 912369 GTCGGACAGAGGAGTTGGGGGGCGGGCCCGGGAGTGGGGGCGCGGACCCGGGAGTGGGGGCGAAG GTCGGACAGAGGAGTTGGGGGGCGGGCCCGGGGGTGGGGGCGCGGACCCGGGAGTGGGGGCGAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:912352..912732 26863196 MeRIP-seq:(Medium) rs1196417425 Functional Loss SNV dbSNP153 33..33 33 - - - 80166 RMVar_ID_80166 Human_SNP_ID_655215471 m1A Human chr19 + 912829 912829 912829 AAATGGGGACGTGGATCCGGGTCCCCTCCCCCAGCGAGCCCCCGGAGCGCCAGGAGGGTGTCCCC AAATGGGGACGTGGATCCGGGTCCCCTCCCCCTGCGAGCCCCCGGAGCGCCAGGAGGGTGTCCCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:912826..912922 26863196 MeRIP-seq:(Medium) rs1228014264 Functional Loss SNV dbSNP153 33..33 33 - - - 80167 RMVar_ID_80167 Human_SNP_ID_655215536 m1A Human chr19 + 912992 912992 912992 AGCGAGGGGAACGAAGGGAACGAGGGGAGGGAAGGGAAAGGAGGGGAGGGGAGGCGGGGAGAGGA AGCGAGGGGAACGAAGGGAACGAGGGGAGGGAGGGGAAAGGAGGGGAGGGGAGGCGGGGAGAGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:912988..913167 26863196 MeRIP-seq:(Medium) rs1450020785 Functional Loss SNV dbSNP153 33..33 33 - - - 80168 RMVar_ID_80168 Human_SNP_ID_655215564 m1A Human chr19 + 913034 913034 913034 GGGGAGGGGAGGCGGGGAGAGGATCTCAGGGGAGGGAGCCCAGCCCGCCCCCGGCGCCCGCCGCG GGGGAGGGGAGGCGGGGAGAGGATCTCAGGGGGGGGAGCCCAGCCCGCCCCCGGCGCCCGCCGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:913032..913200 26863410 MeRIP-seq:(Medium) rs1017231165 Functional Loss SNV dbSNP153 33..33 33 - - - 80169 RMVar_ID_80169 Human_SNP_ID_655215646 m1A Human chr19 + 913156 913156 913156 CCGGGCCGCACTCGGGGTTCTCCAGCGCGACCATGGCTCGCACGCTGTCGCCGCCGCCGCCGCCC CCGGGCCGCACTCGGGGTTCTCCAGCGCGACCGTGGCTCGCACGCTGTCGCCGCCGCCGCCGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:902588..913225;chr19:913047..913225;chr19:913029..913225 26863196 MeRIP-seq:(Medium) rs1262146780 Functional Loss SNV dbSNP153 33..33 33 - - - 80170 RMVar_ID_80170 Human_SNP_ID_655218413 m1A Human chr19 - 920428 920428 920428 CGCGTAGGCGGCGTAGCTGCGTGGGTGCCAGGAGCCCGCGGGGCCCAGCGCCTGCAGCACCAGGA CGCGTAGGCGGCGTAGCTGCGTGGGTGCCAGGCGCCCGCGGGGCCCAGCGCCTGCAGCACCAGGA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:920415..920528 26863196 MeRIP-seq:(Medium) rs375252773 Functional Loss SNV dbSNP153 33..33 33 - - - 80171 RMVar_ID_80171 Human_SNP_ID_655220498 m1A Human chr19 - 926192 926192 926192 AACGGCCAGCGCGCTCCCCAGCCTTACCGCGCAGGGCGGCTCGTAGTGGGGCGCGCGCCCCGCGC AACGGCCAGCGCGCTCCCCAGCCTTACCGCGCTGGGCGGCTCGTAGTGGGGCGCGCGCCCCGCGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:926143..926251 32194978 MeRIP-seq:(Medium) rs546294858 Functional Loss SNV dbSNP153 33..33 33 - - - 80172 RMVar_ID_80172 Human_SNP_ID_655221658 m1A Human chr19 + 929315 929315 929315 AGCCGGATGCCAGCCTCTGTCCCCTGGAGCCCAGCGTGAGGAAGAGGCATGCCCCATCAGCCTTC AGCCGGATGCCAGCCTCTGTCCCCTGGAGCCCGGCGTGAGGAAGAGGCATGCCCCATCAGCCTTC A G ARID3A Ensembl:ENSG00000116017 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:929233..929358 26863196 MeRIP-seq:(Medium) rs1203812775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3953883,Human_RBP_ID_4556936,Human_RBP_ID_18421496,Human_RBP_ID_22545182 Human_Splice_Rec_1929614,Human_Splice_Rec_1929616,Human_Splice_Rec_1929632 RMVar_hsa_circ_31646 80173 RMVar_ID_80173 Human_SNP_ID_655222009 m1A Human chr19 - 929896 929896 929896 CCCAGAAGGCCCTGCCCCAGACCCCAACTCACATGTCCTCGTCGGAGGCCATGTCCTCAAAGTGC CCCAGAAGGCCCTGCCCCAGACCCCAACTCACCTGTCCTCGTCGGAGGCCATGTCCTCAAAGTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:929518..932594 26863196 MeRIP-seq:(Medium) rs371181848 Functional Loss SNV dbSNP153 33..33 33 - - - 80174 RMVar_ID_80174 Human_SNP_ID_655222992 m1A Human chr19 + 932378 932378 932378 GGAGTGGGTCTTTCCTTGGGCTGGGACGAGCCAGCACCTTCTCCCCTGACTCCTGCCCTCTGCTC GGAGTGGGTCTTTCCTTGGGCTGGGACGAGCCGGCACCTTCTCCCCTGACTCCTGCCCTCTGCTC A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:932375..932573 26863196 MeRIP-seq:(Medium) rs780655557 Functional Loss SNV dbSNP153 33..33 33 - - - 80175 RMVar_ID_80175 Human_SNP_ID_655232593 m1A Human chr19 + 960146 960146 960146 CCAAGAGGAAGGAATTCCTGGATGACTTGTTCAGCTTCATGCAGAAGCGAGGTGAGCCCTCTGCC CCAAGAGGAAGGAATTCCTGGATGACTTGTTCCGCTTCATGCAGAAGCGAGGTGAGCCCTCTGCC A C ARID3A Ensembl:ENSG00000116017 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:932593..961788 32194978 MeRIP-seq:(Medium) rs1292824667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381499,Human_RBP_ID_23812555 Human_Splice_Rec_1929620,Human_Splice_Rec_1929621,Human_Splice_Rec_1929634,Human_Splice_Rec_1929635,Human_Splice_Rec_1929644,Human_Splice_Rec_1929645 RMVar_hsa_circ_77808,RMVar_hsa_circ_190927,RMVar_hsa_circ_317554,RMVar_hsa_circ_190926,RMVar_hsa_circ_373251,RMVar_hsa_circ_312842 80176 RMVar_ID_80176 Human_SNP_ID_655233873 m1A Human chr19 - 964344 964344 964344 TGGTGATCTCACGCCACAGCTTCTTGTTGATGACCTCCACGAGGCCGCCCTTCTCCGTCACCAGC TGGTGATCTCACGCCACAGCTTCTTGTTGATGCCCTCCACGAGGCCGCCCTTCTCCGTCACCAGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:964293..964844 32194978 MeRIP-seq:(Medium) rs866421579 Functional Loss SNV dbSNP153 33..33 33 - - - 80177 RMVar_ID_80177 Human_SNP_ID_655240481 m1A Human chr19 - 984390 984390 984390 CCACACGATGCAGCTCCACATCGGGGCCGCCGAGTCCGTACACACGGCCACCTCCATGGGCGCCG CCACACGATGCAGCTCCACATCGGGGCCGCCGTGTCCGTACACACGGCCACCTCCATGGGCGCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:984326..984550;chr19:984326..984575 26863196 MeRIP-seq:(Medium) rs1240900377 Functional Loss SNV dbSNP153 33..33 33 - - - 80178 RMVar_ID_80178 Human_SNP_ID_655240514 m1A Human chr19 + 984450 984450 984450 TGTGGGAACTTCACTCGGGCGCCAACCTGCTCACCTACCGCGGCGGCCAGGCGGGACCCCGCGGC TGTGGGAACTTCACTCGGGCGCCAACCTGCTCGCCTACCGCGGCGGCCAGGCGGGACCCCGCGGC A G WDR18 Ensembl:ENSG00000065268 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:984401..989898 32194978 MeRIP-seq:(Medium) rs1408675571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1019453,Human_RBP_ID_4556712,Human_RBP_ID_8942094,Human_RBP_ID_17934664,Human_RBP_ID_18191543,Human_RBP_ID_22447095 80179 RMVar_ID_80179 Human_SNP_ID_655240516 m1A Human chr19 - 984453 984453 984453 CAGGCCGCGGGGTCCCGCCTGGCCGCCGCGGTAGGTGAGCAGGTTGGCGCCCGAGTGAAGTTCCC CAGGCCGCGGGGTCCCGCCTGGCCGCCGCGGTGGGTGAGCAGGTTGGCGCCCGAGTGAAGTTCCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:984351..985916 26863410 MeRIP-seq:(Medium) rs748069476 Functional Loss SNV dbSNP153 33..33 33 - - - 80180 RMVar_ID_80180 Human_SNP_ID_655243347 m1A Human chr19 - 991924 991924 991924 GCCTGGGGGGCGCGGAGGTCAGGCCCCGCCCCATCCCAGCCAGGCCCCACCCCACAGCAAGCCAA GCCTGGGGGGCGCGGAGGTCAGGCCCCGCCCCCTCCCAGCCAGGCCCCACCCCACAGCAAGCCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:991919..992045 26863196 MeRIP-seq:(Medium) rs549585472 Functional Loss SNV dbSNP153 33..33 33 - - - 80181 RMVar_ID_80181 Human_SNP_ID_655244325 m1A Human chr19 + 994324 994311 994324 ATCGGGACCTGTTCGACTTCTCCACGCGCTTCATCACGCGGCCGGCCAAGTGAGGCCCGGAGACC ATCGGGACCTGTTCGACTTC_____________TCACGCGGCCGGCCAAGTGAGGCCCGGAGACC CTCCACGCGCTTCA C WDR18 Ensembl:ENSG00000065268 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:994274..994357 26863196 MeRIP-seq:(Medium) rs1237732531 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_3579594,Human_RBP_ID_4556850,Human_RBP_ID_17934702 80182 RMVar_ID_80182 Human_SNP_ID_655244326 m1A Human chr19 - 994312 994312 994312 TCACTTGGCCGGCCGCGTGATGAAGCGCGTGGAGAAGTCGAACAGGTCCCGATTGATCTTGCGCA TCACTTGGCCGGCCGCGTGATGAAGCGCGTGGCGAAGTCGAACAGGTCCCGATTGATCTTGCGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:994262..994374 26863196 MeRIP-seq:(Medium) rs778897782 Functional Loss SNV dbSNP153 33..33 33 - - - 80183 RMVar_ID_80183 Human_SNP_ID_655244332 m1A Human chr19 + 994324 994321 994324 ATCGGGACCTGTTCGACTTCTCCACGCGCTTCATCACGCGGCCGGCCAAGTGAGGCCCGGAGACC ATCGGGACCTGTTCGACTTCTCCACGCGCT___TCACGCGGCCGGCCAAGTGAGGCCCGGAGACC TTCA T WDR18 Ensembl:ENSG00000065268 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:994274..994357 26863196 MeRIP-seq:(Medium) rs1440263926 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3579594,Human_RBP_ID_4556850,Human_RBP_ID_17934702 80184 RMVar_ID_80184 Human_SNP_ID_655250702 m1A Human chr19 + 1009797 1009797 1009797 CGGCCCACTCCATCCCCGAGTGGGACTGGACCACGGCCCTGGCTGCTGCCACTGATGTTGGCGCC CGGCCCACTCCATCCCCGAGTGGGACTGGACCTCGGCCCTGGCTGCTGCCACTGATGTTGGCGCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr19:1009751..1009946;chr19:1009747..1009897 26863196,32194978 MeRIP-seq:(Medium) rs1055359483 Functional Loss SNV dbSNP153 33..33 33 - - - 80185 RMVar_ID_80185 Human_SNP_ID_655250845 m1A Human chr19 + 1010135 1010135 1010135 CCGCGGAACCCCACCCCCTCTCCTTGCTGACCAGCTCAAACACCTCACTAGCGGGTACAAGCCTC CCGCGGAACCCCACCCCCTCTCCTTGCTGACCCGCTCAAACACCTCACTAGCGGGTACAAGCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1009701..1010900 26863196 MeRIP-seq:(Medium) rs1004315136 Functional Loss SNV dbSNP153 33..33 33 - - - 80186 RMVar_ID_80186 Human_SNP_ID_655251016 m1A Human chr19 + 1010462 1010462 1010462 TTGTGTCAGAAGCTGCGGAGTCACTCGGGGGGACACTGTCCTGGGGGGCGTGGGGGAGGCCCCCA TTGTGTCAGAAGCTGCGGAGTCACTCGGGGGGGCACTGTCCTGGGGGGCGTGGGGGAGGCCCCCA A G AC004528.2 Ensembl:ENSG00000274177 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1010451..1010646 26863196 MeRIP-seq:(Medium) rs1190761786 Functional Loss SNV dbSNP153 33..33 33 - - - 80187 RMVar_ID_80187 Human_SNP_ID_655251046 m1A Human chr19 + 1010494 1010494 1010494 ACACTGTCCTGGGGGGCGTGGGGGAGGCCCCCAGCAGGGCCCAGCGGGCTGGCTGGACGCCGCTC ACACTGTCCTGGGGGGCGTGGGGGAGGCCCCCGGCAGGGCCCAGCGGGCTGGCTGGACGCCGCTC A G AC004528.2 Ensembl:ENSG00000274177 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1010076..1010875 32194978 MeRIP-seq:(Medium) rs757457166 Functional Loss SNV dbSNP153 33..33 33 - - - 80188 RMVar_ID_80188 Human_SNP_ID_655251069 m1A Human chr19 - 1010525 1010525 1010525 CTTCCTGTCCGGCCTGAGCGCCTCCCTCCTGGAGCGGCGTCCAGCCAGCCCGCTGGGCCCTGCTG CTTCCTGTCCGGCCTGAGCGCCTCCCTCCTGGTGCGGCGTCCAGCCAGCCCGCTGGGCCCTGCTG T A TMEM259 Ensembl:ENSG00000182087 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1010244..1010907 26863410 MeRIP-seq:(Medium) rs1458946231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55578,Human_RBP_ID_240986,Human_RBP_ID_511853,Human_RBP_ID_1012687,Human_RBP_ID_17272221,Human_RBP_ID_17913973,Human_RBP_ID_22533241 80189 RMVar_ID_80189 Human_SNP_ID_655251947 m1A Human chr19 - 1011994 1011994 1011994 TGGGGGCGGGCGCTCACGGCTCCTTCTGCTGCAGGCTTCCTGCGGAATGTGGTGTCGGGCGAGCA TGGGGGCGGGCGCTCACGGCTCCTTCTGCTGCGGGCTTCCTGCGGAATGTGGTGTCGGGCGAGCA T C TMEM259 Ensembl:ENSG00000182087 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1011872..1012184;chr19:1011966..1012246 26863196 MeRIP-seq:(Medium) rs113403992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909908,Human_RBP_ID_4560595,Human_RBP_ID_5374649,Human_RBP_ID_18993884,Human_RBP_ID_22546436 RMVar_hsa_circ_190931,RMVar_hsa_circ_332195,RMVar_hsa_circ_373084,RMVar_hsa_circ_122636,RMVar_hsa_circ_190930,RMVar_hsa_circ_88980,RMVar_hsa_circ_117438,RMVar_hsa_circ_190937,RMVar_hsa_circ_190938,RMVar_hsa_circ_190936,RMVar_hsa_circ_110525,RMVar_hsa_circ_111530,RMVar_hsa_circ_190939,RMVar_hsa_circ_190941 80190 RMVar_ID_80190 Human_SNP_ID_655252287 m1A Human chr19 + 1012532 1012532 1012532 GCGGGTGGCCTGCGACAGGCGAAGGAAGCCATACTCTAGTGAGTACTCCACGATGTACTCGTCCT GCGGGTGGCCTGCGACAGGCGAAGGAAGCCATGCTCTAGTGAGTACTCCACGATGTACTCGTCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1012460..1012575 32194978 MeRIP-seq:(Medium) rs758740479 Functional Loss SNV dbSNP153 33..33 33 - - - 80191 RMVar_ID_80191 Human_SNP_ID_655252289 m1A Human chr19 - 1012539 1012539 1012539 TGGCCGCAGGACGAGTACATCGTGGAGTACTCACTAGAGTATGGCTTCCTTCGCCTGTCGCAGGC TGGCCGCAGGACGAGTACATCGTGGAGTACTCGCTAGAGTATGGCTTCCTTCGCCTGTCGCAGGC T C TMEM259 Ensembl:ENSG00000182087 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1012490..1012568 26863196 MeRIP-seq:(Medium) rs764341636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54620,Human_RBP_ID_511869,Human_RBP_ID_1879246,Human_RBP_ID_22977548,Human_RBP_ID_26335011 Human_Splice_Rec_1929798,Human_Splice_Rec_1929799,Human_Splice_Rec_1929818,Human_Splice_Rec_1929819,Human_Splice_Rec_1929836,Human_Splice_Rec_1929837,Human_Splice_Rec_1929864,Human_Splice_Rec_1929882,Human_Splice_Rec_1929883,Human_Splice_Rec_1929908,Human_Splice_Rec_1929909,Human_Splice_Rec_1929916,Human_Splice_Rec_1929922,Human_Splice_Rec_1929923,Human_Splice_Rec_1929926 Human_miRNA_ID_1971599,Human_miRNA_ID_2383243,Human_miRNA_ID_3004780 RMVar_hsa_circ_190931,RMVar_hsa_circ_332195,RMVar_hsa_circ_373084,RMVar_hsa_circ_122636,RMVar_hsa_circ_190930,RMVar_hsa_circ_117438,RMVar_hsa_circ_190937,RMVar_hsa_circ_190938,RMVar_hsa_circ_110525,RMVar_hsa_circ_190939 80192 RMVar_ID_80192 Human_SNP_ID_655252557 m1A Human chr19 - 1013295 1013295 1013295 TCGAGCCCAAGGTGTTCAAGCCGCCGAGTAGCACAGAGGCCCTGAATGACAGCCAGGAGTTCCCC TCGAGCCCAAGGTGTTCAAGCCGCCGAGTAGCGCAGAGGCCCTGAATGACAGCCAGGAGTTCCCC T C TMEM259 Ensembl:ENSG00000182087 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1013204..1013366 26863196 MeRIP-seq:(Medium) rs1451147487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54621,Human_RBP_ID_240733,Human_RBP_ID_511872,Human_RBP_ID_772220,Human_RBP_ID_909911,Human_RBP_ID_1879247,Human_RBP_ID_4497233,Human_RBP_ID_5115919,Human_RBP_ID_17694418,Human_RBP_ID_18993891,Human_RBP_ID_22426357,Human_RBP_ID_26334761,Human_RBP_ID_27815724 Human_Splice_Rec_1929796,Human_Splice_Rec_1929797,Human_Splice_Rec_1929816,Human_Splice_Rec_1929817,Human_Splice_Rec_1929834,Human_Splice_Rec_1929835,Human_Splice_Rec_1929862,Human_Splice_Rec_1929863,Human_Splice_Rec_1929880,Human_Splice_Rec_1929881,Human_Splice_Rec_1929907,Human_Splice_Rec_1929914,Human_Splice_Rec_1929915,Human_Splice_Rec_1929920,Human_Splice_Rec_1929921,Human_Splice_Rec_1929925 Human_miRNA_ID_2354336,Human_miRNA_ID_2574806,Human_miRNA_ID_2766065 RMVar_hsa_circ_373084,RMVar_hsa_circ_122636,RMVar_hsa_circ_190930,RMVar_hsa_circ_190938,RMVar_hsa_circ_110525,RMVar_hsa_circ_190939 80193 RMVar_ID_80193 Human_SNP_ID_655254920 m1A Human chr19 - 1020756 1020756 1020756 TCTTCGTGCTGCTCAAGGTGACCGCGGCCCCGACCCCCGACCCTTGACCCCAGCGGCTGTCCCGA TCTTCGTGCTGCTCAAGGTGACCGCGGCCCCGGCCCCCGACCCTTGACCCCAGCGGCTGTCCCGA T C TMEM259 Ensembl:ENSG00000182087 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:1020751..1021125;chr19:1020751..1020775 26863196 MeRIP-seq:(Medium) rs1225380960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19091168,Human_RBP_ID_26784640 RMVar_hsa_circ_122636,RMVar_hsa_circ_190938,RMVar_hsa_circ_110525,RMVar_hsa_circ_190939 80194 RMVar_ID_80194 Human_SNP_ID_655255019 m1A Human chr19 + 1020995 1020995 1020995 GCCCCGGAGCTGCGGGCTCCACGTGCTCCGACATGCCTCCCAGCGTCGCGCCCTAACGACCCGCA GCCCCGGAGCTGCGGGCTCCACGTGCTCCGACGTGCCTCCCAGCGTCGCGCCCTAACGACCCGCA A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:1020897..1021075 26863410 MeRIP-seq:(Medium) rs1485949520 Functional Loss SNV dbSNP153 33..33 33 - - - 80195 RMVar_ID_80195 Human_SNP_ID_655255037 m1A Human chr19 - 1021032 1021032 1021032 GGCGGCCGATGGCGGCCGGGAGGCGCCCTCGGACACTTGCGGGTCGTTAGGGCGCGACGCTGGGA GGCGGCCGATGGCGGCCGGGAGGCGCCCTCGGTCACTTGCGGGTCGTTAGGGCGCGACGCTGGGA T A TMEM259 Ensembl:ENSG00000182087 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1020751..1021125 26863196 MeRIP-seq:(Medium) rs917144967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4556949,Human_RBP_ID_23780548,Human_RBP_ID_27561899 RMVar_hsa_circ_122636,RMVar_hsa_circ_190938,RMVar_hsa_circ_110525,RMVar_hsa_circ_190939 80196 RMVar_ID_80196 Human_SNP_ID_655255055 m1A Human chr19 + 1021086 1021086 1021086 CATCGGCCGCCCTCGCAGCCGCCGCTCTCCTCACGGCCTCCCGGCCGCCGCCGCCATCTTCCGCT CATCGGCCGCCCTCGCAGCCGCCGCTCTCCTCCCGGCCTCCCGGCCGCCGCCGCCATCTTCCGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1020708..1021175;chr19:1020719..1021175;chr19:1020733..1021150 26863196 MeRIP-seq:(Medium) rs1172002519 Functional Loss SNV dbSNP153 33..33 33 - - - 80197 RMVar_ID_80197 Human_SNP_ID_655257277 m1A Human chr19 - 1026663 1026663 1026663 ACGAGGGGCCCTTGTTGAACTGCGTGGAGCTCATGGCTGGCGGGCGGGCGGCGGGACGGGGCCGC ACGAGGGGCCCTTGTTGAACTGCGTGGAGCTCGTGGCTGGCGGGCGGGCGGCGGGACGGGGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1026601..1026829;chr19:1026601..1026795 26863196 MeRIP-seq:(Medium) rs1208741110 Functional Loss SNV dbSNP153 33..33 33 - - - 80198 RMVar_ID_80198 Human_SNP_ID_655257278 m1A Human chr19 - 1026663 1026663 1026663 ACGAGGGGCCCTTGTTGAACTGCGTGGAGCTCATGGCTGGCGGGCGGGCGGCGGGACGGGGCCGC ACGAGGGGCCCTTGTTGAACTGCGTGGAGCTCCTGGCTGGCGGGCGGGCGGCGGGACGGGGCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1026601..1026829;chr19:1026601..1026795 26863196 MeRIP-seq:(Medium) rs1208741110 Functional Loss SNV dbSNP153 33..33 33 - - - 80199 RMVar_ID_80199 Human_SNP_ID_655259579 m1A Human chr19 + 1033524 1033524 1033524 CTCTCTCAAAAAATAATCATAACAAAAGTAATAAATAAGCTCTGAACTGGGAGAAATGCCTTGAA CTCTCTCAAAAAATAATCATAACAAAAGTAATCAATAAGCTCTGAACTGGGAGAAATGCCTTGAA A C CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1033519..1033693 26863196 MeRIP-seq:(Medium) rs1237445240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1187008,Human_RBP_ID_8476073 RMVar_hsa_circ_108455,RMVar_hsa_circ_127267,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_125242,RMVar_hsa_circ_80000,RMVar_hsa_circ_190947,RMVar_hsa_circ_190949,RMVar_hsa_circ_190950,RMVar_hsa_circ_190948,RMVar_hsa_circ_117682,RMVar_hsa_circ_326474,RMVar_hsa_circ_82013,RMVar_hsa_circ_190951,RMVar_hsa_circ_190953,RMVar_hsa_circ_190952 80200 RMVar_ID_80200 Human_SNP_ID_655259944 m1A Human chr19 + 1035091 1035090 1035092 GGTGTCTGGTGTATACCGGGAGCGTGGGTGGGACACGGTGTCTGGTGTAGACGGGGAGCGTGGGT GGTGTCTGGTGTATACCGGGAGCGTGGGTGGG__ACGGTGTCTGGTGTAGACGGGGAGCGTGGGT GAC G CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1035087..1035215 26863196 MeRIP-seq:(Medium) rs1406794130 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8194990,Human_RBP_ID_18944504 RMVar_hsa_circ_108455,RMVar_hsa_circ_127267,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_125242,RMVar_hsa_circ_80000,RMVar_hsa_circ_190947,RMVar_hsa_circ_190949,RMVar_hsa_circ_190950,RMVar_hsa_circ_190948,RMVar_hsa_circ_117682,RMVar_hsa_circ_326474,RMVar_hsa_circ_82013,RMVar_hsa_circ_190951,RMVar_hsa_circ_190953,RMVar_hsa_circ_190952 80201 RMVar_ID_80201 Human_SNP_ID_655260948 m1A Human chr19 + 1037695 1037695 1037695 TGATACCAAGCTGGGAACCGACAAGTGTGACAACTCCTCCATGTCCCTGCAGATGGGCTACACGC TGATACCAAGCTGGGAACCGACAAGTGTGACAGCTCCTCCATGTCCCTGCAGATGGGCTACACGC A G CNN2 Ensembl:ENSG00000064666 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1037630..1037744 26863196 MeRIP-seq:(Medium) rs1215258651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512011,Human_RBP_ID_18191546 Human_Splice_Rec_1929946,Human_Splice_Rec_1929956,Human_Splice_Rec_1929968,Human_Splice_Rec_1929986,Human_Splice_Rec_1930000,Human_Splice_Rec_1930030 RMVar_hsa_circ_127267,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_190950,RMVar_hsa_circ_82013,RMVar_hsa_circ_90361,RMVar_hsa_circ_190951,RMVar_hsa_circ_82862,RMVar_hsa_circ_190957,RMVar_hsa_circ_88569,RMVar_hsa_circ_190960,RMVar_hsa_circ_190962,RMVar_hsa_circ_109529,RMVar_hsa_circ_190963 80202 RMVar_ID_80202 Human_SNP_ID_655260949 m1A Human chr19 + 1037695 1037695 1037695 TGATACCAAGCTGGGAACCGACAAGTGTGACAACTCCTCCATGTCCCTGCAGATGGGCTACACGC TGATACCAAGCTGGGAACCGACAAGTGTGACATCTCCTCCATGTCCCTGCAGATGGGCTACACGC A T CNN2 Ensembl:ENSG00000064666 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1037630..1037744 26863196 MeRIP-seq:(Medium) rs1215258651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512011,Human_RBP_ID_18191546 Human_Splice_Rec_1929946,Human_Splice_Rec_1929956,Human_Splice_Rec_1929968,Human_Splice_Rec_1929986,Human_Splice_Rec_1930000,Human_Splice_Rec_1930030 RMVar_hsa_circ_127267,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_190950,RMVar_hsa_circ_82013,RMVar_hsa_circ_90361,RMVar_hsa_circ_190951,RMVar_hsa_circ_82862,RMVar_hsa_circ_190957,RMVar_hsa_circ_88569,RMVar_hsa_circ_190960,RMVar_hsa_circ_190962,RMVar_hsa_circ_109529,RMVar_hsa_circ_190963 80203 RMVar_ID_80203 Human_SNP_ID_655261441 m1A Human chr19 + 1038899 1038899 1038899 CCCAGCCCCTCAGTAGGTTTTAAGGAGCCCCCAGCCCTCCTCCCTTCTGGGCCCGACCAGCTTAT CCCAGCCCCTCAGTAGGTTTTAAGGAGCCCCCGGCCCTCCTCCCTTCTGGGCCCGACCAGCTTAT A G CNN2 Ensembl:ENSG00000064666 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1038626..1038950 32194978 MeRIP-seq:(Medium) rs1439847725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769934,Human_RBP_ID_8197084,Human_RBP_ID_13357585,Human_RBP_ID_17386516,Human_RBP_ID_23173423,Human_RBP_ID_26463914 Human_miRNA_ID_2030493,Human_miRNA_ID_2686009,Human_miRNA_ID_2690948,Human_miRNA_ID_2694260 RMVar_hsa_circ_127267,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_190950,RMVar_hsa_circ_82013,RMVar_hsa_circ_90361,RMVar_hsa_circ_190951,RMVar_hsa_circ_82862,RMVar_hsa_circ_190957,RMVar_hsa_circ_88569,RMVar_hsa_circ_190960,RMVar_hsa_circ_190962,RMVar_hsa_circ_109529,RMVar_hsa_circ_190963 80204 RMVar_ID_80204 Human_SNP_ID_655261452 m1A Human chr19 - 1038928 1038928 1038928 GGGCATGTGGCCGGGGAAGATGGAGCAGTATAAGCTGGTCGGGCCCAGAAGGGAGGAGGGCTGGG GGGCATGTGGCCGGGGAAGATGGAGCAGTATACGCTGGTCGGGCCCAGAAGGGAGGAGGGCTGGG T G AC011558.1 Ensembl:ENSG00000279753 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1038710..1039027 26863196 MeRIP-seq:(Medium) rs778573188 Functional Loss SNV dbSNP153 33..33 33 - - - 80205 RMVar_ID_80205 Human_SNP_ID_655266595 m1A Human chr19 + 1049755 1049755 1049755 CCCCACCACTCCCTCCCCGTGAACCCCCCACCACTCCCTCCCCGTGAGCCCCCCCACCACTCCCT CCCCACCACTCCCTCCCCGTGAACCCCCCACCCCTCCCTCCCCGTGAGCCCCCCCACCACTCCCT A C ABCA7 Ensembl:ENSG00000064687 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1049670..1049838 26863410 MeRIP-seq:(Medium) rs1487346814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69944,RMVar_hsa_circ_73438,RMVar_hsa_circ_67424 80206 RMVar_ID_80206 Human_SNP_ID_655266596 m1A Human chr19 + 1049755 1049755 1049755 CCCCACCACTCCCTCCCCGTGAACCCCCCACCACTCCCTCCCCGTGAGCCCCCCCACCACTCCCT CCCCACCACTCCCTCCCCGTGAACCCCCCACCGCTCCCTCCCCGTGAGCCCCCCCACCACTCCCT A G ABCA7 Ensembl:ENSG00000064687 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1049670..1049838 26863410 MeRIP-seq:(Medium) rs1487346814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69944,RMVar_hsa_circ_73438,RMVar_hsa_circ_67424 80207 RMVar_ID_80207 Human_SNP_ID_655274352 m1A Human chr19 + 1067689 1067689 1067689 CCCGGCATTCAGCTCACGGTAGGGACCCTGGGAGTGGTGGCCGCCTCCCTCCACTCCATCCAGGG CCCGGCATTCAGCTCACGGTAGGGACCCTGGGGGTGGTGGCCGCCTCCCTCCACTCCATCCAGGG A G ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1067686..1067902 26863196 MeRIP-seq:(Medium) rs1188828453 Functional Loss SNV dbSNP153 33..33 33 - - - 80208 RMVar_ID_80208 Human_SNP_ID_655276602 m1A Human chr19 - 1074437 1074437 1074437 AATGGGGCTGAGACTCACACCCGGGCCCAGGGACCCCCGCCCCGTGCCCGCGGGGCCCCCACCTC AATGGGGCTGAGACTCACACCCGGGCCCAGGGCCCCCCGCCCCGTGCCCGCGGGGCCCCCACCTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1074426..1074450 26863196 MeRIP-seq:(Medium) rs942226123 Functional Loss SNV dbSNP153 33..33 33 - - - 80209 RMVar_ID_80209 Human_SNP_ID_655278666 m1A Human chr19 - 1079674 1079674 1079674 CCGCCTGCGGTGGGGGCGGGGCGCACAGAGAGAGGCCTCAGCCCGGGGTGCAGGACTCAGACAGA CCGCCTGCGGTGGGGGCGGGGCGCACAGAGAGCGGCCTCAGCCCGGGGTGCAGGACTCAGACAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1079670..1079781 26863196 MeRIP-seq:(Medium) rs1419040969 Functional Loss SNV dbSNP153 33..33 33 - - - 80210 RMVar_ID_80210 Human_SNP_ID_655280192 m1A Human chr19 + 1082911 1082911 1082911 CTCGTAGGGCTGGCCAAGGACAGCCTGAAGGCAGAGGCCGAGGCCAAGGCGGCGTCCCGGGGCCG CTCGTAGGGCTGGCCAAGGACAGCCTGAAGGCGGAGGCCGAGGCCAAGGCGGCGTCCCGGGGCCG A G ARHGAP45 Ensembl:ENSG00000180448 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1082906..1083008 26863196 MeRIP-seq:(Medium) rs773601777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1930432,Human_Splice_Rec_1930480,Human_Splice_Rec_1930520,Human_Splice_Rec_1930570,Human_Splice_Rec_1930614,Human_Splice_Rec_1930656,Human_Splice_Rec_1930692,Human_Splice_Rec_1930702,Human_Splice_Rec_1930704 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 80211 RMVar_ID_80211 Human_SNP_ID_655281325 m1A Human chr19 - 1085452 1085424 1085452 GATGGAGAGACATGGCGGGGAGGAGGAGAGAGAGACAAGGGGAGAAACGGAAGGAGAGAGGTGTT GATGGAGAGACATGGCGGGGAGGAGGAGAGAG____________________________GTGTT CCTCTCTCCTTCCGTTTCTCCCCTTGTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1085401..1085719 26863196 MeRIP-seq:(Medium) rs1252179116 Functional Loss DEL dbSNP153 33..60 33 - - - Human_RBP_ID_512472 80212 RMVar_ID_80212 Human_SNP_ID_655281343 m1A Human chr19 - 1085452 1085449 1085453 GATGGAGAGACATGGCGGGGAGGAGGAGAGAGAGACAAGGGGAGAAACGGAAGGAGAGAGGTGTT GATGGAGAGACATGGCGGGGAGGAGGAGAGA____CAAGGGGAGAAACGGAAGGAGAGAGGTGTT GTCTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1085401..1085719 26863196 MeRIP-seq:(Medium) rs767721737 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_512472 80213 RMVar_ID_80213 Human_SNP_ID_655281344 m1A Human chr19 - 1085452 1085449 1085453 GATGGAGAGACATGGCGGGGAGGAGGAGAGAGAGACAAGGGGAGAAACGGAAGGAGAGAGGTGTT GATGGAGAGACATGGCGGGGAGGAGGAGAGA__GACAAGGGGAGAAACGGAAGGAGAGAGGTGTT GTCTC GTC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1085401..1085719 26863196 MeRIP-seq:(Medium) rs767721737 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_512472 80214 RMVar_ID_80214 Human_SNP_ID_655281378 m1A Human chr19 - 1085489 1085489 1085489 AGGAGAGATGGAGGAGAGACAAGGGGAGGGACAGACAGATGGAGAGACATGGCGGGGAGGAGGAG AGGAGAGATGGAGGAGAGACAAGGGGAGGGACGGACAGATGGAGAGACATGGCGGGGAGGAGGAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:1085467..1085596 26863196 MeRIP-seq:(Medium) rs1262639219 Functional Loss SNV dbSNP153 33..33 33 - - - 80215 RMVar_ID_80215 Human_SNP_ID_655281499 m1A Human chr19 + 1085579 1085561 1085580 CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCATCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCATCTCTCTCCCCC___________________CTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCTCTCCTGTCTCTCCCCAT C ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1085430..1085668 26863196 MeRIP-seq:(Medium) rs886549043 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_20433160 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 80216 RMVar_ID_80216 Human_SNP_ID_655281499 m1A Human chr19 - 1085580 1085561 1085580 AGGAGAGACAAGGGGAGGGACAGACAGGAGAGATGGGGAGAGACAGGAGAGGGGGGAGAGAGATG AGGAGAGACAAGGGGAGGGACAGACAGGAGAG___________________GGGGGAGAGAGATG CCTCTCCTGTCTCTCCCCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1085366..1085685;chr19:1085401..1085677 26863196 MeRIP-seq:(Medium) rs886549043 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_6717900 80217 RMVar_ID_80217 Human_SNP_ID_655281514 m1A Human chr19 + 1085579 1085569 1085579 CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCATCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCATCTCTCTCCCCCCTCTCCTG__________TCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC GTCTCTCCCCA G ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1085430..1085668 26863196 MeRIP-seq:(Medium) rs951971399 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_20433160 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 80218 RMVar_ID_80218 Human_SNP_ID_655281528 m1A Human chr19 + 1085579 1085579 1085579 CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCATCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCCTCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC A C ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1085430..1085668 26863196 MeRIP-seq:(Medium) rs1489039298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20433160 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 80219 RMVar_ID_80219 Human_SNP_ID_655281529 m1A Human chr19 + 1085579 1085579 1085579 CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCATCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCGTCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC A G ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1085430..1085668 26863196 MeRIP-seq:(Medium) rs1489039298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20433160 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 80220 RMVar_ID_80220 Human_SNP_ID_655281907 m1A Human chr19 - 1086014 1086014 1086014 GCAAGAGAGAAGCCACCTGTGGTCCCAGCCCCACCCCAGCTCACACGAATTCCGGCTGCCTTTCC GCAAGAGAGAAGCCACCTGTGGTCCCAGCCCCGCCCCAGCTCACACGAATTCCGGCTGCCTTTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1085964..1086084 26863196 MeRIP-seq:(Medium) rs1568493690 Functional Loss SNV dbSNP153 33..33 33 - - - 80221 RMVar_ID_80221 Human_SNP_ID_655281977 m1A Human chr19 - 1086095 1086095 1086095 AGGCGCTCTCGGCAGCGACCCCAGGACGGCGCACCTAAGCTATGCCGTGGTGCAGGGGACGTGCT AGGCGCTCTCGGCAGCGACCCCAGGACGGCGCGCCTAAGCTATGCCGTGGTGCAGGGGACGTGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1085928..1086578 32194978 MeRIP-seq:(Medium) rs1448988717 Functional Loss SNV dbSNP153 33..33 33 - - - 80222 RMVar_ID_80222 Human_SNP_ID_655283190 m1A Human chr19 + 1088376 1088376 1088376 CCGAGGGAGGGAAGACGAGGGGTGGAAGGCCGAGGGCCCAGGAGGAAGCAGTGGCTGGTGGGAGA CCGAGGGAGGGAAGACGAGGGGTGGAAGGCCGCGGGCCCAGGAGGAAGCAGTGGCTGGTGGGAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1088262..1088398 26863196 MeRIP-seq:(Medium) rs1386008455 Functional Loss SNV dbSNP153 33..33 33 - - - 80223 RMVar_ID_80223 Human_SNP_ID_655283227 m1A Human chr19 + 1088459 1088459 1088459 AACAGAGGGGACCCAGCGTGGTCTGGGTGAAGACCCGGCACCAGCTGCCCCCAGGTGACCTCCCT AACAGAGGGGACCCAGCGTGGTCTGGGTGAAGCCCCGGCACCAGCTGCCCCCAGGTGACCTCCCT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1088451..1088500 26863196 MeRIP-seq:(Medium) rs1422391118 Functional Loss SNV dbSNP153 33..33 33 - - - 80224 RMVar_ID_80224 Human_SNP_ID_655283228 m1A Human chr19 + 1088459 1088459 1088459 AACAGAGGGGACCCAGCGTGGTCTGGGTGAAGACCCGGCACCAGCTGCCCCCAGGTGACCTCCCT AACAGAGGGGACCCAGCGTGGTCTGGGTGAAGTCCCGGCACCAGCTGCCCCCAGGTGACCTCCCT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1088451..1088500 26863196 MeRIP-seq:(Medium) rs1422391118 Functional Loss SNV dbSNP153 33..33 33 - - - 80225 RMVar_ID_80225 Human_SNP_ID_655283721 m1A Human chr19 + 1089493 1089493 1089493 GGCCGTCTCACCTGTCAGGCGGTAGCTACTGCACCAGCCGGTAGGTGATGTACCTGCCAGCCGTC GGCCGTCTCACCTGTCAGGCGGTAGCTACTGCCCCAGCCGGTAGGTGATGTACCTGCCAGCCGTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1088216..1091000 32194978 MeRIP-seq:(Medium) rs753834886 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 80226 RMVar_ID_80226 Human_SNP_ID_655284434 m1A Human chr19 - 1090867 1090867 1090867 GCGCCGCGGAATCCCGCCTGCGTGGGGCCGGCAGAGATGCAGCGTTTGTGGGTGGCCAGGAAGAT GCGCCGCGGAATCCCGCCTGCGTGGGGCCGGCGGAGATGCAGCGTTTGTGGGTGGCCAGGAAGAT T C POLR2E Ensembl:ENSG00000099817 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1090866..1090940 26863196 MeRIP-seq:(Medium) rs754548590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5370854,Human_RBP_ID_19088356 RMVar_hsa_circ_81258,RMVar_hsa_circ_84576,RMVar_hsa_circ_104627,RMVar_hsa_circ_29423,RMVar_hsa_circ_190977,RMVar_hsa_circ_125341,RMVar_hsa_circ_375778,RMVar_hsa_circ_190981,RMVar_hsa_circ_190982,RMVar_hsa_circ_11738,RMVar_hsa_circ_190984 80227 RMVar_ID_80227 Human_SNP_ID_655285945 m1A Human chr19 + 1094064 1094064 1094064 TGGTCAAGCTCGTCCTGGGTCACCAGATAGCCACGGTCGTGGCACAGCTGCAGAGAGAAAGAACC TGGTCAAGCTCGTCCTGGGTCACCAGATAGCCGCGGTCGTGGCACAGCTGCAGAGAGAAAGAACC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:1094026..1094100 26863410 MeRIP-seq:(Medium) rs1195196173 Functional Loss SNV dbSNP153 33..33 33 - - - 80228 RMVar_ID_80228 Human_SNP_ID_655285946 m1A Human chr19 + 1094064 1094064 1094064 TGGTCAAGCTCGTCCTGGGTCACCAGATAGCCACGGTCGTGGCACAGCTGCAGAGAGAAAGAACC TGGTCAAGCTCGTCCTGGGTCACCAGATAGCCTCGGTCGTGGCACAGCTGCAGAGAGAAAGAACC A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:1094026..1094100 26863410 MeRIP-seq:(Medium) rs1195196173 Functional Loss SNV dbSNP153 33..33 33 - - - 80229 RMVar_ID_80229 Human_SNP_ID_655286417 m1A Human chr19 + 1095314 1095314 1095314 TCCAGAGCCGGTACGTCTCCTCCTCGTCGTCCATGGCAGCCTCCGCCGCCGCCGCCGCTCGCACC TCCAGAGCCGGTACGTCTCCTCCTCGTCGTCCCTGGCAGCCTCCGCCGCCGCCGCCGCTCGCACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1095192..1095375 26863196 MeRIP-seq:(Medium) rs1269111832 Functional Loss SNV dbSNP153 33..33 33 - - - 80230 RMVar_ID_80230 Human_SNP_ID_655286418 m1A Human chr19 + 1095314 1095314 1095314 TCCAGAGCCGGTACGTCTCCTCCTCGTCGTCCATGGCAGCCTCCGCCGCCGCCGCCGCTCGCACC TCCAGAGCCGGTACGTCTCCTCCTCGTCGTCCTTGGCAGCCTCCGCCGCCGCCGCCGCTCGCACC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1095192..1095375 26863196 MeRIP-seq:(Medium) rs1269111832 Functional Loss SNV dbSNP153 33..33 33 - - - 80231 RMVar_ID_80231 Human_SNP_ID_655289427 m1A Human chr19 + 1104125 1104125 1104125 GGGCTCTGGCCGCGCCTGGCCTGGCCGGGACCATGGTGAGCTAGCGCCGCGGCCGTTGCCGGCCC GGGCTCTGGCCGCGCCTGGCCTGGCCGGGACCGTGGTGAGCTAGCGCCGCGGCCGTTGCCGGCCC A G GPX4 Ensembl:ENSG00000167468 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1104076..1104221 26863196 MeRIP-seq:(Medium) rs925722714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241768,Human_RBP_ID_530325,Human_RBP_ID_4556956,Human_RBP_ID_5144798,Human_RBP_ID_5319750,Human_RBP_ID_19088360,Human_RBP_ID_22069371,Human_RBP_ID_22447108,Human_RBP_ID_26769727 Human_Splice_Rec_1930873,Human_Splice_Rec_1930885,Human_Splice_Rec_1930897,Human_Splice_Rec_1930907,Human_Splice_Rec_1930919,Human_Splice_Rec_1930929 80232 RMVar_ID_80232 Human_SNP_ID_655289853 m1A Human chr19 + 1105226 1105226 1105226 CCGGGACGACTGGCGCTGTGCGCGCTCCATGCACGAGTTTTCCGCCAAGGACATCGACGGGCACA CCGGGACGACTGGCGCTGTGCGCGCTCCATGCGCGAGTTTTCCGCCAAGGACATCGACGGGCACA A G GPX4 Ensembl:ENSG00000167468 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1105183..1105528 26863196 MeRIP-seq:(Medium) rs1045408258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512671,Human_RBP_ID_1554067,Human_RBP_ID_1879791,Human_RBP_ID_4556958,Human_RBP_ID_5319755,Human_RBP_ID_8476620,Human_RBP_ID_9084331,Human_RBP_ID_9328016,Human_RBP_ID_9381526,Human_RBP_ID_22446278,Human_RBP_ID_26464212,Human_RBP_ID_26982066 Human_Splice_Rec_1930874,Human_Splice_Rec_1930875,Human_Splice_Rec_1930886,Human_Splice_Rec_1930887,Human_Splice_Rec_1930898,Human_Splice_Rec_1930899,Human_Splice_Rec_1930908,Human_Splice_Rec_1930909,Human_Splice_Rec_1930920,Human_Splice_Rec_1930921,Human_Splice_Rec_1930930,Human_Splice_Rec_1930931,Human_Splice_Rec_1930942,Human_Splice_Rec_1930943,Human_Splice_Rec_1930948,Human_Splice_Rec_1930949,Human_Splice_Rec_1930960,Human_Splice_Rec_1930961,Human_Splice_Rec_1930963,Human_Splice_Rec_1930973 Human_miRNA_ID_2218659,Human_miRNA_ID_2218660,Human_miRNA_ID_2794503,Human_miRNA_ID_2794504,Human_miRNA_ID_2794969,Human_miRNA_ID_2794970,Human_miRNA_ID_2795436,Human_miRNA_ID_2795437 RMVar_hsa_circ_88406,RMVar_hsa_circ_87071,RMVar_hsa_circ_190989,RMVar_hsa_circ_370246,RMVar_hsa_circ_190991,RMVar_hsa_circ_81395,RMVar_hsa_circ_190992,RMVar_hsa_circ_190990 80233 RMVar_ID_80233 Human_SNP_ID_655290603 m1A Human chr19 + 1106437 1106437 1106437 CATCGACAAGAACGGCTGCGTGGTGAAGCGCTACGGACCCATGGAGGAGCCCCTGGTAGGTCCTC CATCGACAAGAACGGCTGCGTGGTGAAGCGCTGCGGACCCATGGAGGAGCCCCTGGTAGGTCCTC A G GPX4 Ensembl:ENSG00000167468 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1106254..1106742 32194978 MeRIP-seq:(Medium) rs1416229761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512684,Human_RBP_ID_912820,Human_RBP_ID_4499964,Human_RBP_ID_17656467,Human_RBP_ID_19088368,Human_RBP_ID_26816473 Human_Splice_Rec_1930882,Human_Splice_Rec_1930883,Human_Splice_Rec_1930894,Human_Splice_Rec_1930895,Human_Splice_Rec_1930904,Human_Splice_Rec_1930905,Human_Splice_Rec_1930916,Human_Splice_Rec_1930917,Human_Splice_Rec_1930928,Human_Splice_Rec_1930938,Human_Splice_Rec_1930939,Human_Splice_Rec_1930956,Human_Splice_Rec_1930957,Human_Splice_Rec_1930970,Human_Splice_Rec_1930971,Human_Splice_Rec_1930978,Human_Splice_Rec_1930979,Human_Splice_Rec_1930988,Human_Splice_Rec_1930989 RMVar_hsa_circ_82082,RMVar_hsa_circ_88406,RMVar_hsa_circ_370246,RMVar_hsa_circ_190991,RMVar_hsa_circ_190992,RMVar_hsa_circ_87826,RMVar_hsa_circ_190993,RMVar_hsa_circ_190994 80234 RMVar_ID_80234 Human_SNP_ID_655290688 m1A Human chr19 - 1106556 1106556 1106556 CCACACACTTGTGGAGCTAGAAATAGTGGGGCAGGTCCTTCTCTATCACCTGTCGGGGAGGAAAG CCACACACTTGTGGAGCTAGAAATAGTGGGGCGGGTCCTTCTCTATCACCTGTCGGGGAGGAAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr19:1106374..1106756;chr19:1106401..1106702 26863196 MeRIP-seq:(Medium) rs1191177439 Functional Loss SNV dbSNP153 33..33 33 - - - 80235 RMVar_ID_80235 Human_SNP_ID_655290707 m1A Human chr19 - 1106586 1106586 1106586 CCAAGGGCGTGGGCAGGGGCTCGGGCGGGGCCACACACTTGTGGAGCTAGAAATAGTGGGGCAGG CCAAGGGCGTGGGCAGGGGCTCGGGCGGGGCCGCACACTTGTGGAGCTAGAAATAGTGGGGCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1106457..1106732 26863196 MeRIP-seq:(Medium) rs371481974 Functional Loss SNV dbSNP153 33..33 33 - - - 80236 RMVar_ID_80236 Human_SNP_ID_655290708 m1A Human chr19 - 1106586 1106586 1106586 CCAAGGGCGTGGGCAGGGGCTCGGGCGGGGCCACACACTTGTGGAGCTAGAAATAGTGGGGCAGG CCAAGGGCGTGGGCAGGGGCTCGGGCGGGGCCCCACACTTGTGGAGCTAGAAATAGTGGGGCAGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1106457..1106732 26863196 MeRIP-seq:(Medium) rs371481974 Functional Loss SNV dbSNP153 33..33 33 - - - 80237 RMVar_ID_80237 Human_SNP_ID_655290772 m1A Human chr19 + 1106691 1106691 1106691 GCTGGTGGGGCAGACCCGAAAATCCAGCGTGCACCCCGCCGGAGGAAGGTCCCATGGCCTGCTGG GCTGGTGGGGCAGACCCGAAAATCCAGCGTGCGCCCCGCCGGAGGAAGGTCCCATGGCCTGCTGG A G GPX4 Ensembl:ENSG00000167468 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1106642..1106742 32194978 MeRIP-seq:(Medium) rs948854873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512692,Human_RBP_ID_4561369,Human_RBP_ID_5421135,Human_RBP_ID_5498873,Human_RBP_ID_17914562,Human_RBP_ID_18208582,Human_RBP_ID_18721909,Human_RBP_ID_22592812,Human_RBP_ID_23781448,Human_RBP_ID_24374740,Human_RBP_ID_26464223,Human_RBP_ID_26982078,Human_RBP_ID_27267301,Human_RBP_ID_27463033 Human_miRNA_ID_2147283,Human_miRNA_ID_2988710,Human_miRNA_ID_3022409 RMVar_hsa_circ_82082,RMVar_hsa_circ_88406,RMVar_hsa_circ_190992,RMVar_hsa_circ_190993 80238 RMVar_ID_80238 Human_SNP_ID_655291433 m1A Human chr19 + 1108179 1108179 1108179 CCCTGCTCCCCACCGCTGCTCCTAGGGGAGAAACGGTCCCTGTGTCTTGGGGCATGTTTCGCCTA CCCTGCTCCCCACCGCTGCTCCTAGGGGAGAAGCGGTCCCTGTGTCTTGGGGCATGTTTCGCCTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1108176..1108550 26863196 MeRIP-seq:(Medium) rs1390590538 Functional Loss SNV dbSNP153 33..33 33 - - - 80239 RMVar_ID_80239 Human_SNP_ID_655291434 m1A Human chr19 + 1108179 1108179 1108179 CCCTGCTCCCCACCGCTGCTCCTAGGGGAGAAACGGTCCCTGTGTCTTGGGGCATGTTTCGCCTA CCCTGCTCCCCACCGCTGCTCCTAGGGGAGAATCGGTCCCTGTGTCTTGGGGCATGTTTCGCCTA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1108176..1108550 26863196 MeRIP-seq:(Medium) rs1390590538 Functional Loss SNV dbSNP153 33..33 33 - - - 80240 RMVar_ID_80240 Human_SNP_ID_655291511 m1A Human chr19 - 1108264 1108264 1108264 CGGCGGGCGGTGGTCCCGAGCGGCAGAGCGTGATCCAGTTCAGCCCACCCTTCCCCGGCGCCCAG CGGCGGGCGGTGGTCCCGAGCGGCAGAGCGTGTTCCAGTTCAGCCCACCCTTCCCCGGCGCCCAG T A SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1108262..1108550 26863196 MeRIP-seq:(Medium) rs765952457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3953937,Human_RBP_ID_19091192,Human_RBP_ID_26784658 RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995 80241 RMVar_ID_80241 Human_SNP_ID_655291606 m1A Human chr19 - 1108404 1108404 1108404 CGCCCAGGCCGACCCTGCGGCCCTCGCGCACCAGGGCTGCGACATCAACTTCAAGGAGGTGCTGG CGCCCAGGCCGACCCTGCGGCCCTCGCGCACCGGGGCTGCGACATCAACTTCAAGGAGGTGCTGG T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1108367..1108483 26863196 MeRIP-seq:(Medium) rs1477275108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27463039 RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995 80242 RMVar_ID_80242 Human_SNP_ID_655291619 m1A Human chr19 - 1108431 1108431 1108431 CGGCGTCGTGCCGCTGGGCACCCCCGACGCCCAGGCCGACCCTGCGGCCCTCGCGCACCAGGGCT CGGCGTCGTGCCGCTGGGCACCCCCGACGCCCGGGCCGACCCTGCGGCCCTCGCGCACCAGGGCT T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1108380..1108497 26863196 MeRIP-seq:(Medium) rs1229186625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995 80243 RMVar_ID_80243 Human_SNP_ID_655291645 m1A Human chr19 - 1108473 1108473 1108473 GCACTTCTCTTTCCCGGCGCCGCTGTCCCTGGACGCCGGCCCCGGCGTCGTGCCGCTGGGCACCC GCACTTCTCTTTCCCGGCGCCGCTGTCCCTGGGCGCCGGCCCCGGCGTCGTGCCGCTGGGCACCC T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1108233..1108610 26863410 MeRIP-seq:(Medium) rs559278372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293107,Human_RBP_ID_27463041 RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995 80244 RMVar_ID_80244 Human_SNP_ID_655291879 m1A Human chr19 - 1108844 1108844 1108844 CGTGTGGGGCCGCATCGCCGCCGTCATGGCCGACGTCAGCAGCAGCAGCTACCTGCAGATCGTGC CGTGTGGGGCCGCATCGCCGCCGTCATGGCCGGCGTCAGCAGCAGCAGCTACCTGCAGATCGTGC T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1108726..1108912 26863196 MeRIP-seq:(Medium) rs1327000840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293108,Human_RBP_ID_18191550 Human_Splice_Rec_1931045,Human_Splice_Rec_1931107,Human_Splice_Rec_1931169,Human_Splice_Rec_1931181 RMVar_hsa_circ_31583,RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_121503,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995,RMVar_hsa_circ_265145,RMVar_hsa_circ_110593,RMVar_hsa_circ_119630,RMVar_hsa_circ_104909,RMVar_hsa_circ_190999,RMVar_hsa_circ_191001,RMVar_hsa_circ_191002,RMVar_hsa_circ_191000 80245 RMVar_ID_80245 Human_SNP_ID_655291916 m1A Human chr19 + 1108893 1108893 1108893 GATGCGGCCCCACACGCGCAGCAGCGCGCCGCACAGCATGTAGTGGTGCCGCAGCCGCAGCCCCT GATGCGGCCCCACACGCGCAGCAGCGCGCCGCCCAGCATGTAGTGGTGCCGCAGCCGCAGCCCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1108790..1108892 26863196 MeRIP-seq:(Medium) rs777977913 Functional Loss SNV dbSNP153 33..33 33 - - - 80246 RMVar_ID_80246 Human_SNP_ID_655292815 m1A Human chr19 + 1110487 1110487 1110487 ACCCTCGCTCACCCAGGATGCATGGCGCTTCCACGAGCCCCTTGCCCACCTAGGCCCTCGCCGTG ACCCTCGCTCACCCAGGATGCATGGCGCTTCCGCGAGCCCCTTGCCCACCTAGGCCCTCGCCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1110476..1110575 26863196 MeRIP-seq:(Medium) rs888182657 Functional Loss SNV dbSNP153 33..33 33 - - - 80247 RMVar_ID_80247 Human_SNP_ID_655294604 m1A Human chr19 + 1114352 1114352 1114352 AGGCCAGGGTCCGACTCCGTGCTGCTGTCGTCACTGATGCGGATGACGCCCGCTGTCTCGCACGC AGGCCAGGGTCCGACTCCGTGCTGCTGTCGTCGCTGATGCGGATGACGCCCGCTGTCTCGCACGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1114318..1114462 26863196 MeRIP-seq:(Medium) rs1377135098 Functional Loss SNV dbSNP153 33..33 33 - - - 80248 RMVar_ID_80248 Human_SNP_ID_655295338 m1A Human chr19 + 1116098 1116098 1116098 ACGGAAAGTGCTTCTGAATTAGCGACAGGAACACGCCTCTGAAAGTGAGACGCGGAGTTTATTCT ACGGAAAGTGCTTCTGAATTAGCGACAGGAACGCGCCTCTGAAAGTGAGACGCGGAGTTTATTCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1116026..1119027 32194978 MeRIP-seq:(Medium) rs1324966473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13364313 80249 RMVar_ID_80249 Human_SNP_ID_655295572 m1A Human chr19 - 1116805 1116805 1116805 GGCCGCTGAGTAAGTGTCACGGTGGGGACAGGACTGTGGGCTTCCTGCGCTCATGGCCACCCCTC GGCCGCTGAGTAAGTGTCACGGTGGGGACAGGGCTGTGGGCTTCCTGCGCTCATGGCCACCCCTC T C SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1116802..1116878 26863196 MeRIP-seq:(Medium) rs774886263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359444 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190998,RMVar_hsa_circ_190997,RMVar_hsa_circ_110593,RMVar_hsa_circ_104909,RMVar_hsa_circ_97654,RMVar_hsa_circ_190999,RMVar_hsa_circ_191000,RMVar_hsa_circ_68142,RMVar_hsa_circ_125063,RMVar_hsa_circ_191004,RMVar_hsa_circ_191006 80250 RMVar_ID_80250 Human_SNP_ID_655295573 m1A Human chr19 - 1116805 1116805 1116805 GGCCGCTGAGTAAGTGTCACGGTGGGGACAGGACTGTGGGCTTCCTGCGCTCATGGCCACCCCTC GGCCGCTGAGTAAGTGTCACGGTGGGGACAGGCCTGTGGGCTTCCTGCGCTCATGGCCACCCCTC T G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1116802..1116878 26863196 MeRIP-seq:(Medium) rs774886263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359444 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190998,RMVar_hsa_circ_190997,RMVar_hsa_circ_110593,RMVar_hsa_circ_104909,RMVar_hsa_circ_97654,RMVar_hsa_circ_190999,RMVar_hsa_circ_191000,RMVar_hsa_circ_68142,RMVar_hsa_circ_125063,RMVar_hsa_circ_191004,RMVar_hsa_circ_191006 80251 RMVar_ID_80251 Human_SNP_ID_655298124 m1A Human chr19 - 1122992 1122992 1122992 CAGACCGCGTGGTGGAGACCAGCACACTGTCCAGCGTCCCACCCCCAGACATCACCTACACCCTG CAGACCGCGTGGTGGAGACCAGCACACTGTCCGGCGTCCCACCCCCAGACATCACCTACACCCTG T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1122941..1123044 26863196 MeRIP-seq:(Medium) rs1026785967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8476727 Human_Splice_Rec_1930998,Human_Splice_Rec_1930999,Human_Splice_Rec_1931060,Human_Splice_Rec_1931061,Human_Splice_Rec_1931122,Human_Splice_Rec_1931123,Human_Splice_Rec_1931194,Human_Splice_Rec_1931195 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_190998,RMVar_hsa_circ_190997,RMVar_hsa_circ_110593,RMVar_hsa_circ_104909,RMVar_hsa_circ_190999,RMVar_hsa_circ_191000,RMVar_hsa_circ_68142,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_110103,RMVar_hsa_circ_191009 80252 RMVar_ID_80252 Human_SNP_ID_655298350 m1A Human chr19 - 1123516 1123516 1123516 ACGTGCCGTCCAAGTGTGAGTGGCCCGGCTGCACCCAGCCCTGGGACAGGTTCAAACCCTTTTGT ACGTGCCGTCCAAGTGTGAGTGGCCCGGCTGCGCCCAGCCCTGGGACAGGTTCAAACCCTTTTGT T C SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1123512..1123577 26863196 MeRIP-seq:(Medium) rs772039349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19091203 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_190998,RMVar_hsa_circ_110593,RMVar_hsa_circ_190999,RMVar_hsa_circ_68142,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_110103,RMVar_hsa_circ_191009 80253 RMVar_ID_80253 Human_SNP_ID_655298354 m1A Human chr19 + 1123519 1123519 1123519 AAAGGGTTTGAACCTGTCCCAGGGCTGGGTGCAGCCGGGCCACTCACACTTGGACGGCACGTAGT AAAGGGTTTGAACCTGTCCCAGGGCTGGGTGCGGCCGGGCCACTCACACTTGGACGGCACGTAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1123516..1123650 26863196 MeRIP-seq:(Medium) rs1273993854 Functional Loss SNV dbSNP153 33..33 33 - - - 80254 RMVar_ID_80254 Human_SNP_ID_655300959 m1A Human chr19 + 1131073 1131073 1131073 AGCTCCCCCCACAGTGGCTCCGTCCTCTGCCCACATCTGGATTTGACTCCTAGCAGCCACCAGCT AGCTCCCCCCACAGTGGCTCCGTCCTCTGCCCGCATCTGGATTTGACTCCTAGCAGCCACCAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1131064..1131235 26863196 MeRIP-seq:(Medium) rs1454680616 Functional Loss SNV dbSNP153 33..33 33 - - - 80255 RMVar_ID_80255 Human_SNP_ID_655304821 m1A Human chr19 - 1142212 1142184 1142212 TCGTGAGGGAGGTCATTGAGGGAGGGTTGATCATGAGGGAGGTCATTGAGTGAGGGTTGATCATG TCGTGAGGGAGGTCATTGAGGGAGGGTTGATC____________________________TCATG ATCAACCCTCACTCAATGACCTCCCTCAT A SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1141981..1142253 26863196 MeRIP-seq:(Medium) rs1298495429 Functional Loss DEL dbSNP153 33..60 33 - - - Human_RBP_ID_263450,Human_RBP_ID_3579853,Human_RBP_ID_5190924,Human_RBP_ID_5319757,Human_RBP_ID_8101239,Human_RBP_ID_8195028,Human_RBP_ID_8232927,Human_RBP_ID_8942287,Human_RBP_ID_9425049,Human_RBP_ID_18944531,Human_RBP_ID_22416572,Human_RBP_ID_26784663 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_190998,RMVar_hsa_circ_110593,RMVar_hsa_circ_190999,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80256 RMVar_ID_80256 Human_SNP_ID_655304846 m1A Human chr19 - 1142212 1142212 1142212 TCGTGAGGGAGGTCATTGAGGGAGGGTTGATCATGAGGGAGGTCATTGAGTGAGGGTTGATCATG TCGTGAGGGAGGTCATTGAGGGAGGGTTGATCTTGAGGGAGGTCATTGAGTGAGGGTTGATCATG T A SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1141981..1142253 26863196 MeRIP-seq:(Medium) rs147180074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263450,Human_RBP_ID_3579853,Human_RBP_ID_5190924,Human_RBP_ID_5319757,Human_RBP_ID_8101239,Human_RBP_ID_8195028,Human_RBP_ID_8232927,Human_RBP_ID_8942287,Human_RBP_ID_9425049,Human_RBP_ID_18944531,Human_RBP_ID_22416572,Human_RBP_ID_26784663 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_190998,RMVar_hsa_circ_110593,RMVar_hsa_circ_190999,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80257 RMVar_ID_80257 Human_SNP_ID_655304847 m1A Human chr19 - 1142212 1142212 1142212 TCGTGAGGGAGGTCATTGAGGGAGGGTTGATCATGAGGGAGGTCATTGAGTGAGGGTTGATCATG TCGTGAGGGAGGTCATTGAGGGAGGGTTGATCGTGAGGGAGGTCATTGAGTGAGGGTTGATCATG T C SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1141981..1142253 26863196 MeRIP-seq:(Medium) rs147180074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263450,Human_RBP_ID_3579853,Human_RBP_ID_5190924,Human_RBP_ID_5319757,Human_RBP_ID_8101239,Human_RBP_ID_8195028,Human_RBP_ID_8232927,Human_RBP_ID_8942287,Human_RBP_ID_9425049,Human_RBP_ID_18944531,Human_RBP_ID_22416572,Human_RBP_ID_26784663 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_190998,RMVar_hsa_circ_110593,RMVar_hsa_circ_190999,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80258 RMVar_ID_80258 Human_SNP_ID_655305308 m1A Human chr19 - 1143697 1143697 1143697 CTCATGAGAGGAGGCGGGAGGGTGAGAGCCAGAGAGAGACGGGAAGAGCCTGCGCTCTGGCCGTG CTCATGAGAGGAGGCGGGAGGGTGAGAGCCAGGGAGAGACGGGAAGAGCCTGCGCTCTGGCCGTG T C SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1143692..1143819 26863196 MeRIP-seq:(Medium) rs527929493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582080 RMVar_hsa_circ_31583,RMVar_hsa_circ_121696,RMVar_hsa_circ_190998,RMVar_hsa_circ_110593,RMVar_hsa_circ_190999,RMVar_hsa_circ_125063,RMVar_hsa_circ_191006,RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80259 RMVar_ID_80259 Human_SNP_ID_655305735 m1A Human chr19 + 1144870 1144861 1144871 AGGGGCAGAGACAAGCAGAGAGGGAGACACAGACAGAGACAGAGAGGGAGACAGAGAGACAGAGG AGGGGCAGAGACAAGCAGAGAGGG__________AGAGACAGAGAGGGAGACAGAGAGACAGAGG GAGACACAGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1144868..1144937 26863196 MeRIP-seq:(Medium) rs1194251479 Functional Loss DEL dbSNP153 25..34 33 - - - 80260 RMVar_ID_80260 Human_SNP_ID_655307374 m1A Human chr19 + 1149322 1149322 1149322 GCACCCAGAACTCCGTTTGTAACTGTGACTTCAGAATGAGCAAGCCTGGGGGCCAGGCGGGGAGG GCACCCAGAACTCCGTTTGTAACTGTGACTTCGGAATGAGCAAGCCTGGGGGCCAGGCGGGGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1149319..1149494 26863196 MeRIP-seq:(Medium) rs1466194489 Functional Loss SNV dbSNP153 33..33 33 - - - 80261 RMVar_ID_80261 Human_SNP_ID_655309223 m1A Human chr19 - 1154353 1154353 1154353 ACCGCCGCCACCACGGAGCGAGAAGCCCAGATAGACGCCCCGGCGGCCCCGGGTCCTGGAGTCCC ACCGCCGCCACCACGGAGCGAGAAGCCCAGATGGACGCCCCGGCGGCCCCGGGTCCTGGAGTCCC T C SBNO2 Ensembl:ENSG00000064932 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1147337..1168869 26863196 MeRIP-seq:(Medium) rs1394774589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4561526 Human_Splice_Rec_1931048,Human_Splice_Rec_1931110,Human_Splice_Rec_1931220,Human_Splice_Rec_1931228,Human_Splice_Rec_1931236 RMVar_hsa_circ_10543,RMVar_hsa_circ_31583,RMVar_hsa_circ_122774,RMVar_hsa_circ_327452,RMVar_hsa_circ_191010,RMVar_hsa_circ_191011 80262 RMVar_ID_80262 Human_SNP_ID_655309248 m1A Human chr19 - 1154396 1154396 1154396 CAGGACGTCCCCGTCTCCCTCTGCAGATCATGATGCTGCCGCCACCGCCGCCACCACGGAGCGAG CAGGACGTCCCCGTCTCCCTCTGCAGATCATGCTGCTGCCGCCACCGCCGCCACCACGGAGCGAG T G SBNO2 Ensembl:ENSG00000064932 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1147383..1155104 26863410 MeRIP-seq:(Medium) rs112016043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6718699 Human_Splice_Rec_1931048,Human_Splice_Rec_1931110,Human_Splice_Rec_1931220,Human_Splice_Rec_1931228,Human_Splice_Rec_1931236 RMVar_hsa_circ_10543,RMVar_hsa_circ_31583,RMVar_hsa_circ_122774,RMVar_hsa_circ_327452,RMVar_hsa_circ_191010,RMVar_hsa_circ_191011 80263 RMVar_ID_80263 Human_SNP_ID_655311241 m1A Human chr19 + 1159502 1159501 1159502 CAGTTGGGGACAGCAGGGGACAGTGGGGGGACAGGGGGCAGCAGGGGACAGTTGGGGACAGCAGG CAGTTGGGGACAGCAGGGGACAGTGGGGGGAC_GGGGGCAGCAGGGGACAGTTGGGGACAGCAGG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1159493..1159603 32194978 MeRIP-seq:(Medium) rs1195520954 Functional Loss DEL dbSNP153 33..33 33 - - - 80264 RMVar_ID_80264 Human_SNP_ID_655311244 m1A Human chr19 + 1159502 1159502 1159502 CAGTTGGGGACAGCAGGGGACAGTGGGGGGACAGGGGGCAGCAGGGGACAGTTGGGGACAGCAGG CAGTTGGGGACAGCAGGGGACAGTGGGGGGACGGGGGGCAGCAGGGGACAGTTGGGGACAGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1159493..1159603 32194978 MeRIP-seq:(Medium) rs1260457632 Functional Loss SNV dbSNP153 33..33 33 - - - 80265 RMVar_ID_80265 Human_SNP_ID_655312205 m1A Human chr19 - 1161926 1161922 1161926 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCA____CCCCCCCCCCCCCCCCGCGGCTCCCCAGG GGGGT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1444723892 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80266 RMVar_ID_80266 Human_SNP_ID_655312206 m1A Human chr19 - 1161926 1161923 1161926 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCA___CCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GGGT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1451670210 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80267 RMVar_ID_80267 Human_SNP_ID_655312209 m1A Human chr19 - 1161926 1161924 1161927 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCC___CCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GGTT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1167729073 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80268 RMVar_ID_80268 Human_SNP_ID_655312210 m1A Human chr19 - 1161926 1161924 1161926 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCA__CCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GGT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1388042926 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80269 RMVar_ID_80269 Human_SNP_ID_655312215 m1A Human chr19 - 1161926 1161925 1161927 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCC__CCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1179828090 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80270 RMVar_ID_80270 Human_SNP_ID_655312216 m1A Human chr19 - 1161926 1161925 1161926 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCA_CCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GT G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1391620639 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80271 RMVar_ID_80271 Human_SNP_ID_655312218 m1A Human chr19 - 1161926 1161926 1161926 GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCAACCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG GTATGTCGGCTCCTCCCCGCAGGCCTGGCCCACCCCCCCCCCCCCCCCCCCCGCGGCTCCCCAGG T G SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1161901..1161925 26863196 MeRIP-seq:(Medium) rs1211606914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80272 RMVar_ID_80272 Human_SNP_ID_655315329 m1A Human chr19 + 1168986 1168986 1168986 CCGGAACCTGGCGCACATCACTTTCAAAACGCAGCGGGGCCTGGAACCAAGGCCAAGGCCGCCTC CCGGAACCTGGCGCACATCACTTTCAAAACGCTGCGGGGCCTGGAACCAAGGCCAAGGCCGCCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1168982..1169161 26863196 MeRIP-seq:(Medium) rs904763030 Functional Loss SNV dbSNP153 33..33 33 - - - 80273 RMVar_ID_80273 Human_SNP_ID_655315353 m1A Human chr19 + 1169035 1169035 1169035 AGGCCAAGGCCGCCTCTTTCGGTTTCACTTGGACGCTTGTTCTTGCTGGGGATGGAGGTCAATCA AGGCCAAGGCCGCCTCTTTCGGTTTCACTTGGTCGCTTGTTCTTGCTGGGGATGGAGGTCAATCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1169031..1169147 26863196 MeRIP-seq:(Medium) rs1003519144 Functional Loss SNV dbSNP153 33..33 33 - - - 80274 RMVar_ID_80274 Human_SNP_ID_655315355 m1A Human chr19 + 1169058 1169036 1169059 TTCACTTGGACGCTTGTTCTTGCTGGGGATGGAGGTCAATCACAAGGCTCCGGGAAGCACGGGCA TTCACTTGGAC_______________________GTCAATCACAAGGCTCCGGGAAGCACGGGCA CGCTTGTTCTTGCTGGGGATGGAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1169042..1169174 32194978 MeRIP-seq:(Medium) rs1475612686 Functional Loss DEL dbSNP153 12..34 33 - - - 80275 RMVar_ID_80275 Human_SNP_ID_655315365 m1A Human chr19 + 1169058 1169058 1169058 TTCACTTGGACGCTTGTTCTTGCTGGGGATGGAGGTCAATCACAAGGCTCCGGGAAGCACGGGCA TTCACTTGGACGCTTGTTCTTGCTGGGGATGGCGGTCAATCACAAGGCTCCGGGAAGCACGGGCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1169042..1169174 32194978 MeRIP-seq:(Medium) rs995321214 Functional Loss SNV dbSNP153 33..33 33 - - - 80276 RMVar_ID_80276 Human_SNP_ID_655316893 m1A Human chr19 - 1173097 1173097 1173097 CGTGGGGGGCAGGCGTTGTGGAGAGCCCACCCAGCGCCTCCAGGGACGCCGGGCACGGATGGTGC CGTGGGGGGCAGGCGTTGTGGAGAGCCCACCCTGCGCCTCCAGGGACGCCGGGCACGGATGGTGC T A SBNO2 Ensembl:ENSG00000064932 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1173094..1173281 26863196 MeRIP-seq:(Medium) rs1366360954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908190,Human_RBP_ID_3579902,Human_RBP_ID_5292556,Human_RBP_ID_5649540,Human_RBP_ID_8099156,Human_RBP_ID_8195118,Human_RBP_ID_8942303,Human_RBP_ID_22719569 RMVar_hsa_circ_122774,RMVar_hsa_circ_191010 80277 RMVar_ID_80277 Human_SNP_ID_655317050 m1A Human chr19 + 1173640 1173640 1173640 AGGAGCCTGGAGTCAGGAATCGGGGCGGCGGGAGAGACCGGGGGTCACTCCCAGGAAGGGGTCGA AGGAGCCTGGAGTCAGGAATCGGGGCGGCGGGTGAGACCGGGGGTCACTCCCAGGAAGGGGTCGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1173631..1173858 26863196 MeRIP-seq:(Medium) rs1358528127 Functional Loss SNV dbSNP153 33..33 33 - - - 80278 RMVar_ID_80278 Human_SNP_ID_655319882 m1A Human chr19 - 1181431 1181424 1181432 AGACAGAGGGACACAGAGACAGAGACAGAGAGACAGAGACAAAGAGAGAGACAGAGAAACAGAGA AGACAGAGGGACACAGAGACAGAGACAGAGA________CAAAGAGAGAGACAGAGAAACAGAGA GTCTCTGTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1181425..1181641 26863196 MeRIP-seq:(Medium) rs1388663774 Functional Loss DEL dbSNP153 32..39 33 - - - 80279 RMVar_ID_80279 Human_SNP_ID_655327349 m1A Human chr19 - 1205924 1205924 1205924 CGCCGCGGCCGCCGCGCGTGTGGAGGAGGCGGAGCGGCGAGGGGGGCCCAGCCCATCCAAGGCCG CGCCGCGGCCGCCGCGCGTGTGGAGGAGGCGGTGCGGCGAGGGGGGCCCAGCCCATCCAAGGCCG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1205822..1206055 26863410 MeRIP-seq:(Medium) rs1218311525 Functional Loss SNV dbSNP153 33..33 33 - - - 80280 RMVar_ID_80280 Human_SNP_ID_655327499 m1A Human chr19 + 1206272 1206272 1206272 GGAGCTGTTGGCCGCGGCGGGAGGCCTCCCGGACGCCCCCAGCCCCCCGAACGCTCGCCCGGGCC GGAGCTGTTGGCCGCGGCGGGAGGCCTCCCGGGCGCCCCCAGCCCCCCGAACGCTCGCCCGGGCC A G STK11 Ensembl:ENSG00000118046 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1206176..1206675 26863410 MeRIP-seq:(Medium) rs915795134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4556967,Human_RBP_ID_5238245 80281 RMVar_ID_80281 Human_SNP_ID_655327842 m1A Human chr19 + 1206977 1206977 1206977 TGTTCACGGAGGGCGAGCTGATGTCGGTGGGTATGGACACGTTCATCCACCGCATCGACTCCACC TGTTCACGGAGGGCGAGCTGATGTCGGTGGGTGTGGACACGTTCATCCACCGCATCGACTCCACC A G STK11 Ensembl:ENSG00000118046 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1206902..1216316 26863410 MeRIP-seq:(Medium) rs1174992777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513035,Human_RBP_ID_909046,Human_RBP_ID_5145499,Human_RBP_ID_6719274,Human_RBP_ID_8829575,Human_RBP_ID_9258932,Human_RBP_ID_9291199,Human_RBP_ID_13367786,Human_RBP_ID_17694551,Human_RBP_ID_17914839,Human_RBP_ID_22501602,Human_RBP_ID_26473037,Human_RBP_ID_27267640,Human_RBP_ID_27463305,Human_RBP_ID_27561961 80282 RMVar_ID_80282 Human_SNP_ID_655327949 m1A Human chr19 - 1207101 1207101 1207101 TGCACAGCGTCTCCGAGTCCAGCACCTCCTTCACCTTGCCGTAAGAGCCTTCCCCCAGCAGGTCC TGCACAGCGTCTCCGAGTCCAGCACCTCCTTCGCCTTGCCGTAAGAGCCTTCCCCCAGCAGGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1206303..1207225 32194978 MeRIP-seq:(Medium) rs1568690276 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_369 80283 RMVar_ID_80283 Human_SNP_ID_655332786 m1A Human chr19 + 1220450 1220449 1220451 GGGCATTGTGCACAAGGACATCAAGCCGGGGAACCTGCTGCTCACCACCGGTGGCACCCTCAAAA GGGCATTGTGCACAAGGACATCAAGCCGGGGGAACTGCTGCTCACCACCGGTGGCACCCTCAAAA AAC GAA STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1220401..1220500 32194978 MeRIP-seq:(Medium) rs1568707668 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_906931,Human_RBP_ID_1554255,Human_RBP_ID_1879949,Human_RBP_ID_6719374,Human_RBP_ID_9329341 Human_Splice_Rec_1931252,Human_Splice_Rec_1931253,Human_Splice_Rec_1931268,Human_Splice_Rec_1931269,Human_Splice_Rec_1931284,Human_Splice_Rec_1931285,Human_Splice_Rec_1931302,Human_Splice_Rec_1931303,Human_Splice_Rec_1931312,Human_Splice_Rec_1931313,Human_Splice_Rec_1931318 Human_miRNA_ID_599651,Human_miRNA_ID_1240306,Human_miRNA_ID_2102265,Human_miRNA_ID_2108220,Human_miRNA_ID_2114160,Human_miRNA_ID_2166704,Human_miRNA_ID_2223691,Human_miRNA_ID_2486763,Human_miRNA_ID_2597962,Human_miRNA_ID_2740868,Human_miRNA_ID_3041454,Human_miRNA_ID_3075126 Clinvar_Rec_370 RMVar_hsa_circ_77058,RMVar_hsa_circ_26746,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017 80284 RMVar_ID_80284 Human_SNP_ID_655332787 m1A Human chr19 + 1220450 1220450 1220450 GGGCATTGTGCACAAGGACATCAAGCCGGGGAACCTGCTGCTCACCACCGGTGGCACCCTCAAAA GGGCATTGTGCACAAGGACATCAAGCCGGGGAGCCTGCTGCTCACCACCGGTGGCACCCTCAAAA A G STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1220401..1220500 32194978 MeRIP-seq:(Medium) rs886037859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906931,Human_RBP_ID_1554255,Human_RBP_ID_1879949,Human_RBP_ID_6719374,Human_RBP_ID_9329341 Human_Splice_Rec_1931252,Human_Splice_Rec_1931253,Human_Splice_Rec_1931268,Human_Splice_Rec_1931269,Human_Splice_Rec_1931284,Human_Splice_Rec_1931285,Human_Splice_Rec_1931302,Human_Splice_Rec_1931303,Human_Splice_Rec_1931312,Human_Splice_Rec_1931313,Human_Splice_Rec_1931318 Human_miRNA_ID_599651,Human_miRNA_ID_1240306,Human_miRNA_ID_2102265,Human_miRNA_ID_2108220,Human_miRNA_ID_2114160,Human_miRNA_ID_2166704,Human_miRNA_ID_2223691,Human_miRNA_ID_2486763,Human_miRNA_ID_2597962,Human_miRNA_ID_2740868,Human_miRNA_ID_3041454,Human_miRNA_ID_3075126 Clinvar_Rec_371 RMVar_hsa_circ_77058,RMVar_hsa_circ_26746,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017 80285 RMVar_ID_80285 Human_SNP_ID_655333238 m1A Human chr19 + 1221263 1221263 1221263 TCTGTACCCCTTCGAAGGGGACAACATCTACAAGTTGTTTGAGAACATCGGGAAGGGGAGCTACG TCTGTACCCCTTCGAAGGGGACAACATCTACAGGTTGTTTGAGAACATCGGGAAGGGGAGCTACG A G STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1220255..1221400 32194978 MeRIP-seq:(Medium) rs1568709214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554257,Human_RBP_ID_1879952,Human_RBP_ID_3955770,Human_RBP_ID_8829591,Human_RBP_ID_9381530,Human_RBP_ID_18722247,Human_RBP_ID_18995724 Human_Splice_Rec_1931256,Human_Splice_Rec_1931257,Human_Splice_Rec_1931272,Human_Splice_Rec_1931273,Human_Splice_Rec_1931288,Human_Splice_Rec_1931289,Human_Splice_Rec_1931306,Human_Splice_Rec_1931320,Human_Splice_Rec_1931321,Human_Splice_Rec_1931324,Human_Splice_Rec_1931325 Human_miRNA_ID_1101238,Human_miRNA_ID_2517668 Clinvar_Rec_372 RMVar_hsa_circ_81149,RMVar_hsa_circ_77058,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017,RMVar_hsa_circ_191018,RMVar_hsa_circ_99642,RMVar_hsa_circ_348053,RMVar_hsa_circ_191019 80286 RMVar_ID_80286 Human_SNP_ID_655334054 m1A Human chr19 + 1223110 1223104 1223110 GCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACA GCCGTACTTGGAGGACCTGCACGGCGC______GGACGAGGACCTCTTCGACATCGAGGATGACA CGGACGA C STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1221926..1223692 32194978 MeRIP-seq:(Medium) rs762810203 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_1879955,Human_RBP_ID_6801047,Human_RBP_ID_8476985,Human_RBP_ID_9381532,Human_RBP_ID_13367953,Human_RBP_ID_18532259,Human_RBP_ID_18722248 Human_Splice_Rec_1931261,Human_Splice_Rec_1931277,Human_Splice_Rec_1931293,Human_Splice_Rec_1931309,Human_Splice_Rec_1931329 Clinvar_Rec_373 RMVar_hsa_circ_81149,RMVar_hsa_circ_77058,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_191013,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017,RMVar_hsa_circ_191019 80287 RMVar_ID_80287 Human_SNP_ID_655334060 m1A Human chr19 + 1223110 1223110 1223110 GCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACA GCCGTACTTGGAGGACCTGCACGGCGCGGACGCGGACGAGGACCTCTTCGACATCGAGGATGACA A C STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1221926..1223692 32194978 MeRIP-seq:(Medium) rs757815836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1879955,Human_RBP_ID_6801047,Human_RBP_ID_8476985,Human_RBP_ID_9381532,Human_RBP_ID_13367953,Human_RBP_ID_18532259,Human_RBP_ID_18722248 Human_Splice_Rec_1931261,Human_Splice_Rec_1931277,Human_Splice_Rec_1931293,Human_Splice_Rec_1931309,Human_Splice_Rec_1931329 Clinvar_Rec_374 RMVar_hsa_circ_81149,RMVar_hsa_circ_77058,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_191013,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017,RMVar_hsa_circ_191019 80288 RMVar_ID_80288 Human_SNP_ID_655334061 m1A Human chr19 + 1223110 1223110 1223110 GCCGTACTTGGAGGACCTGCACGGCGCGGACGAGGACGAGGACCTCTTCGACATCGAGGATGACA GCCGTACTTGGAGGACCTGCACGGCGCGGACGGGGACGAGGACCTCTTCGACATCGAGGATGACA A G STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1221926..1223692 32194978 MeRIP-seq:(Medium) rs757815836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1879955,Human_RBP_ID_6801047,Human_RBP_ID_8476985,Human_RBP_ID_9381532,Human_RBP_ID_13367953,Human_RBP_ID_18532259,Human_RBP_ID_18722248 Human_Splice_Rec_1931261,Human_Splice_Rec_1931277,Human_Splice_Rec_1931293,Human_Splice_Rec_1931309,Human_Splice_Rec_1931329 Clinvar_Rec_374 RMVar_hsa_circ_81149,RMVar_hsa_circ_77058,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_191013,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017,RMVar_hsa_circ_191019 80289 RMVar_ID_80289 Human_SNP_ID_655335432 m1A Human chr19 - 1226584 1226572 1226584 ATCTTGCTGCTGGCGGAGCAGGCCTTGCGGGCAGGGTTGGGGGCCCGGCCCTCCGCCCTGGATTT ATCTTGCTGCTGGCGGAGCAGGCCTTGCGGGC____________CCGGCCCTCCGCCCTGGATTT GGCCCCCAACCCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1226537..1226687 32194978 MeRIP-seq:(Medium) rs1345292099 Functional Loss DEL dbSNP153 33..44 33 - - - 80290 RMVar_ID_80290 Human_SNP_ID_655335444 m1A Human chr19 - 1226584 1226584 1226584 ATCTTGCTGCTGGCGGAGCAGGCCTTGCGGGCAGGGTTGGGGGCCCGGCCCTCCGCCCTGGATTT ATCTTGCTGCTGGCGGAGCAGGCCTTGCGGGCTGGGTTGGGGGCCCGGCCCTCCGCCCTGGATTT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1226537..1226687 32194978 MeRIP-seq:(Medium) rs786201330 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_375 80291 RMVar_ID_80291 Human_SNP_ID_655336679 m1A Human chr19 - 1229088 1229088 1229088 CGGCGGGAGAGACGTGGGGGCGCGACGCCCCGACGCGAATGCGCGGGGACCGCGGGCCCTTCGCG CGGCGGGAGAGACGTGGGGGCGCGACGCCCCGTCGCGAATGCGCGGGGACCGCGGGCCCTTCGCG T A CBARP Ensembl:ENSG00000099625 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1229085..1229435 26863196 MeRIP-seq:(Medium) rs1568724277 Functional Loss SNV dbSNP153 33..33 33 - - - 80292 RMVar_ID_80292 Human_SNP_ID_655337055 m1A Human chr19 + 1229847 1229847 1229847 CTCGCCGTCCTTGGGCCGCGGCGCGGGCGGGGAGGGCGGCGGGAAGGCGGGCGCCGCGCCCCCGG CTCGCCGTCCTTGGGCCGCGGCGCGGGCGGGGGGGGCGGCGGGAAGGCGGGCGCCGCGCCCCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1229833..1230184 26863196 MeRIP-seq:(Medium) rs1234693276 Functional Loss SNV dbSNP153 33..33 33 - - - 80293 RMVar_ID_80293 Human_SNP_ID_655338950 m1A Human chr19 + 1234289 1234289 1234289 GGCTGAGTTGTAGGGGTCACCTGGCAGGGCGGAGCTGGGGCCCACAGAGCGGCCGGTGAGGGCCT GGCTGAGTTGTAGGGGTCACCTGGCAGGGCGGGGCTGGGGCCCACAGAGCGGCCGGTGAGGGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1234284..1234624 26863196 MeRIP-seq:(Medium) rs1009798419 Functional Loss SNV dbSNP153 33..33 33 - - - 80294 RMVar_ID_80294 Human_SNP_ID_655339419 m1A Human chr19 + 1235256 1235220 1235256 GCGGCCACGGCAGGGAGGGCTGGGGCCGCGGCACGGGCGGCCGGGCTGGCGGGGCGAGGGACACT _________________________________CGGGCGGCCGGGCTGGCGGGGCGAGGGACACT CCGGGCGGCCACGGCAGGGAGGGCTGGGGCCGCGGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1235245..1235504 26863196 MeRIP-seq:(Medium) rs1207602036 Functional Loss DEL dbSNP153 1..33 33 - - - 80295 RMVar_ID_80295 Human_SNP_ID_655339439 m1A Human chr19 + 1235256 1235256 1235256 GCGGCCACGGCAGGGAGGGCTGGGGCCGCGGCACGGGCGGCCGGGCTGGCGGGGCGAGGGACACT GCGGCCACGGCAGGGAGGGCTGGGGCCGCGGCGCGGGCGGCCGGGCTGGCGGGGCGAGGGACACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1235245..1235504 26863196 MeRIP-seq:(Medium) rs1185475576 Functional Loss SNV dbSNP153 33..33 33 - - - 80296 RMVar_ID_80296 Human_SNP_ID_655339872 m1A Human chr19 + 1236047 1236041 1236047 TTGTCCCACGACGTCGTCAGGGCTACTGTGGCAGTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC TTGTCCCACGACGTCGTCAGGGCTACT______GTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC TGTGGCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1236042..1236155 26863196 MeRIP-seq:(Medium) rs1478614604 Functional Loss DEL dbSNP153 28..33 33 - - - 80297 RMVar_ID_80297 Human_SNP_ID_655339874 m1A Human chr19 + 1236047 1236044 1236047 TTGTCCCACGACGTCGTCAGGGCTACTGTGGCAGTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC TTGTCCCACGACGTCGTCAGGGCTACTGTG___GTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC GGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1236042..1236155 26863196 MeRIP-seq:(Medium) rs1323452825 Functional Loss DEL dbSNP153 31..33 33 - - - 80298 RMVar_ID_80298 Human_SNP_ID_655339878 m1A Human chr19 - 1236055 1236046 1236055 CCACCATGGCCACAGCCGCCACCACCACCACCACCACCACTGCCACAGTAGCCCTGACGACGTCG CCACCATGGCCACAGCCGCCACCACCACCACC_________GCCACAGTAGCCCTGACGACGTCG CAGTGGTGGT C CBARP Ensembl:ENSG00000099625 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1236043..1237987 26863196 MeRIP-seq:(Medium) rs1218988580 Functional Loss DEL dbSNP153 33..41 33 - - - Human_Splice_Rec_1931334,Human_Splice_Rec_1931335,Human_Splice_Rec_1931350,Human_Splice_Rec_1931351,Human_Splice_Rec_1931368,Human_Splice_Rec_1931369,Human_Splice_Rec_1931388,Human_Splice_Rec_1931389,Human_Splice_Rec_1931416,Human_Splice_Rec_1931417,Human_Splice_Rec_1931426,Human_Splice_Rec_1931427 RMVar_hsa_circ_53087 80299 RMVar_ID_80299 Human_SNP_ID_655339881 m1A Human chr19 + 1236047 1236047 1236047 TTGTCCCACGACGTCGTCAGGGCTACTGTGGCAGTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC TTGTCCCACGACGTCGTCAGGGCTACTGTGGCGGTGGTGGTGGTGGTGGTGGTGGCGGCTGTGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1236042..1236155 26863196 MeRIP-seq:(Medium) rs1345597432 Functional Loss SNV dbSNP153 33..33 33 - - - 80300 RMVar_ID_80300 Human_SNP_ID_655339908 m1A Human chr19 + 1236081 1236081 1236081 TGGTGGTGGTGGTGGTGGTGGCGGCTGTGGCCATGGTGGCTGTGGGCTGCATTCTGAACTGGGGA TGGTGGTGGTGGTGGTGGTGGCGGCTGTGGCCGTGGTGGCTGTGGGCTGCATTCTGAACTGGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1236075..1237988 26863196 MeRIP-seq:(Medium) rs113298601 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_376 80301 RMVar_ID_80301 Human_SNP_ID_655341542 m1A Human chr19 - 1240757 1240754 1240757 ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGG___TTGCAGTGAGCCGAGATCGCGCCACTGCAC ACCT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1240751..1240800 26863196 MeRIP-seq:(Medium) rs1237226835 Functional Loss DEL dbSNP153 33..35 33 - - - 80302 RMVar_ID_80302 Human_SNP_ID_655341543 m1A Human chr19 - 1240757 1240754 1240758 ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC ATAGCTCGAACCCGGGCGGGGGGGGGGGGGG____TTGCAGTGAGCCGAGATCGCGCCACTGCAC ACCTC A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1240751..1240800 26863196 MeRIP-seq:(Medium) rs1568761075 Functional Loss DEL dbSNP153 32..35 33 - - - 80303 RMVar_ID_80303 Human_SNP_ID_655341550 m1A Human chr19 - 1240757 1240755 1240757 ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGG__GTTGCAGTGAGCCGAGATCGCGCCACTGCAC CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1240751..1240800 26863196 MeRIP-seq:(Medium) rs1448465028 Functional Loss DEL dbSNP153 33..34 33 - - - 80304 RMVar_ID_80304 Human_SNP_ID_655341552 m1A Human chr19 - 1240757 1240756 1240757 ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGG_GGTTGCAGTGAGCCGAGATCGCGCCACTGCAC CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1240751..1240800 26863196 MeRIP-seq:(Medium) rs1449596751 Functional Loss DEL dbSNP153 33..33 33 - - - 80305 RMVar_ID_80305 Human_SNP_ID_655341553 m1A Human chr19 - 1240757 1240757 1240757 ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC ATAGCTCGAACCCGGGCGGGGGGGGGGGGGGGGGGTTGCAGTGAGCCGAGATCGCGCCACTGCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1240751..1240800 26863196 MeRIP-seq:(Medium) rs1263060819 Functional Loss SNV dbSNP153 33..33 33 - - - 80306 RMVar_ID_80306 Human_SNP_ID_655341897 m1A Human chr19 + 1241784 1241784 1241784 GACGTCCCTGCGCGTCGTCCTCCTCGCCCTCCAGGCCGCCCGCGCCGCGCCGGAGTCCGCTGTCC GACGTCCCTGCGCGTCGTCCTCCTCGCCCTCCCGGCCGCCCGCGCCGCGCCGGAGTCCGCTGTCC A C ATP5F1D Ensembl:ENSG00000099624 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1241776..1242146 26863196 MeRIP-seq:(Medium) rs866441451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4501537,Human_RBP_ID_5116479,Human_RBP_ID_9328033,Human_RBP_ID_22533056 80307 RMVar_ID_80307 Human_SNP_ID_655341987 m1A Human chr19 - 1241968 1241968 1241968 CGCCCGAACCTGCGTGGGAGAGGCGAAGGTGAAGGACATCTGGTTGGGGCCAGAGGCGGCAGCCG CGCCCGAACCTGCGTGGGAGAGGCGAAGGTGAGGGACATCTGGTTGGGGCCAGAGGCGGCAGCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1241751..1242085 26863196 MeRIP-seq:(Medium) rs1002251968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80308 RMVar_ID_80308 Human_SNP_ID_655341989 m1A Human chr19 - 1241975 1241975 1241975 CCCGCAGCGCCCGAACCTGCGTGGGAGAGGCGAAGGTGAAGGACATCTGGTTGGGGCCAGAGGCG CCCGCAGCGCCCGAACCTGCGTGGGAGAGGCGCAGGTGAAGGACATCTGGTTGGGGCCAGAGGCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1241951..1241975 32194978 MeRIP-seq:(Medium) rs750475776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80309 RMVar_ID_80309 Human_SNP_ID_655342122 m1A Human chr19 - 1242349 1242346 1242349 TAAGTAATGGGTCAGGGCAGGACCTGGCGCTGATGTGAGGCACTGAGACAACCCAGCGCAGGGAT TAAGTAATGGGTCAGGGCAGGACCTGGCGCTG___TGAGGCACTGAGACAACCCAGCGCAGGGAT ACAT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1242346..1242550 26863196 MeRIP-seq:(Medium) rs1332906705 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_191022 80310 RMVar_ID_80310 Human_SNP_ID_655342143 m1A Human chr19 - 1242404 1242403 1242404 GAATGATGGCGGGGCAGGCCGGCCCCGCGCCCACCGGGCACTCGGCCTGTCCTGCTAAGTAATGG GAATGATGGCGGGGCAGGCCGGCCCCGCGCCC_CCGGGCACTCGGCCTGTCCTGCTAAGTAATGG GT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1242402..1242646 26863196 MeRIP-seq:(Medium) rs1568763421 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80311 RMVar_ID_80311 Human_SNP_ID_655342146 m1A Human chr19 - 1242404 1242404 1242404 GAATGATGGCGGGGCAGGCCGGCCCCGCGCCCACCGGGCACTCGGCCTGTCCTGCTAAGTAATGG GAATGATGGCGGGGCAGGCCGGCCCCGCGCCCCCCGGGCACTCGGCCTGTCCTGCTAAGTAATGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1242402..1242646 26863196 MeRIP-seq:(Medium) rs929342060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80312 RMVar_ID_80312 Human_SNP_ID_655342156 m1A Human chr19 - 1242421 1242421 1242421 GCAGACAACAGCGTGGGGAATGATGGCGGGGCAGGCCGGCCCCGCGCCCACCGGGCACTCGGCCT GCAGACAACAGCGTGGGGAATGATGGCGGGGCGGGCCGGCCCCGCGCCCACCGGGCACTCGGCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1242406..1242657 26863196 MeRIP-seq:(Medium) rs1170008551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80313 RMVar_ID_80313 Human_SNP_ID_655342215 m1A Human chr19 - 1242550 1242550 1242550 CTGCATGCACCACGACCAGCCCCGGCCGCAGGACCTGCAGCGTGGGCACGTGGGCCGCCAGGATG CTGCATGCACCACGACCAGCCCCGGCCGCAGGGCCTGCAGCGTGGGCACGTGGGCCGCCAGGATG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1242445..1242646 32194978 MeRIP-seq:(Medium) rs370565722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191022 80314 RMVar_ID_80314 Human_SNP_ID_655342776 m1A Human chr19 + 1244216 1244216 1244216 GGGTGAGTGTCAGAGGGGACCTGAGGCTCAGCAGGTTGGAGCTGTCCAGGCTGCGGGGGAGGGAG GGGTGAGTGTCAGAGGGGACCTGAGGCTCAGCCGGTTGGAGCTGTCCAGGCTGCGGGGGAGGGAG A C ATP5F1D Ensembl:ENSG00000099624 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1244212..1244400 26863196 MeRIP-seq:(Medium) rs1318992412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115923,Human_RBP_ID_19091217 RMVar_hsa_circ_108168,RMVar_hsa_circ_85255,RMVar_hsa_circ_191023,RMVar_hsa_circ_191024 80315 RMVar_ID_80315 Human_SNP_ID_655342832 m1A Human chr19 - 1244330 1244327 1244330 TGTCCCCACCAGCTCCGCCTGGGCCTTCTCCAAGTTTGCCTTGGCTGCCTGCAAGGGGTTGAGGG TGTCCCCACCAGCTCCGCCTGGGCCTTCTCCA___TTGCCTTGGCTGCCTGCAAGGGGTTGAGGG AACT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1244076..1244800 32194978 MeRIP-seq:(Medium) rs1395104131 Functional Loss DEL dbSNP153 33..35 33 - - - 80316 RMVar_ID_80316 Human_SNP_ID_655342833 m1A Human chr19 - 1244330 1244330 1244330 TGTCCCCACCAGCTCCGCCTGGGCCTTCTCCAAGTTTGCCTTGGCTGCCTGCAAGGGGTTGAGGG TGTCCCCACCAGCTCCGCCTGGGCCTTCTCCAGGTTTGCCTTGGCTGCCTGCAAGGGGTTGAGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1244076..1244800 32194978 MeRIP-seq:(Medium) rs761415689 Functional Loss SNV dbSNP153 33..33 33 - - - 80317 RMVar_ID_80317 Human_SNP_ID_655342923 m1A Human chr19 - 1244455 1244455 1244455 CATCCCTGCCCAGCCCCTGGCCGGGCCTCGGGACACCGGGTACGCACCGCCTACTCCAGGGCCTT CATCCCTGCCCAGCCCCTGGCCGGGCCTCGGGGCACCGGGTACGCACCGCCTACTCCAGGGCCTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1244451..1244500 26863196 MeRIP-seq:(Medium) rs774150264 Functional Loss SNV dbSNP153 33..33 33 - - - 80318 RMVar_ID_80318 Human_SNP_ID_655343047 m1A Human chr19 + 1244780 1244780 1244780 AAGGTTGACCTCAGCTTCGGAGCCACCTCTGGATGAACTGCCCCCAGCCCCCGCCCCATTAAAGA AAGGTTGACCTCAGCTTCGGAGCCACCTCTGGTTGAACTGCCCCCAGCCCCCGCCCCATTAAAGA A T ATP5F1D Ensembl:ENSG00000099624 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:1244604..1244825;chr19:1244613..1244825 26863196 MeRIP-seq:(Medium) rs957620330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513097,Human_RBP_ID_3955773,Human_RBP_ID_13368464,Human_RBP_ID_17655740,Human_RBP_ID_18722323,Human_RBP_ID_23782301,Human_RBP_ID_26464433,Human_RBP_ID_26982588,Human_RBP_ID_27463349,Human_RBP_ID_27561968 Human_Splice_Rec_1931444,Human_Splice_Rec_1931456,Human_Splice_Rec_1931468,Human_Splice_Rec_1931474,Human_Splice_Rec_1931480 Human_miRNA_ID_1604416,Human_miRNA_ID_1678666,Human_miRNA_ID_2686014,Human_miRNA_ID_2686015,Human_miRNA_ID_2825996,Human_miRNA_ID_2825997,Human_miRNA_ID_2859969,Human_miRNA_ID_2859970 RMVar_hsa_circ_98777,RMVar_hsa_circ_108168,RMVar_hsa_circ_85255,RMVar_hsa_circ_191023,RMVar_hsa_circ_102521,RMVar_hsa_circ_191024,RMVar_hsa_circ_191025,RMVar_hsa_circ_191026 80319 RMVar_ID_80319 Human_SNP_ID_655345329 m1A Human chr19 + 1249930 1249930 1249930 AGCGGCGGCGACGGCTGTTGCTAAGGGAGGGGACGCGCGAGGAAGCGCGACCCGGGCGGCAGACG AGCGGCGGCGACGGCTGTTGCTAAGGGAGGGGGCGCGCGAGGAAGCGCGACCCGGGCGGCAGACG A G MIDN Ensembl:ENSG00000167470 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1248652..1250094 26863196 MeRIP-seq:(Medium) rs1454444090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4501582,Human_RBP_ID_5319772,Human_RBP_ID_8942105,Human_RBP_ID_22977844,Human_RBP_ID_24559678,Human_RBP_ID_25440634 Human_Splice_Rec_1931482,Human_Splice_Rec_1931490 80320 RMVar_ID_80320 Human_SNP_ID_655345377 m1A Human chr19 + 1250069 1250069 1250069 CGCCCTTTGAAGGAGAAGCAAGTGCCGTCCCCACCCCCGGAAGGCGCCCCCAGGAGCCGGAGCGA CGCCCTTTGAAGGAGAAGCAAGTGCCGTCCCCGCCCCCGGAAGGCGCCCCCAGGAGCCGGAGCGA A G MIDN Ensembl:ENSG00000167470 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1248576..1250227 26863196 MeRIP-seq:(Medium) rs1279890331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559979,Human_RBP_ID_5320824,Human_RBP_ID_22069381 80321 RMVar_ID_80321 Human_SNP_ID_655345402 m1A Human chr19 + 1250108 1250108 1250108 GAAGGCGCCCCCAGGAGCCGGAGCGACCTCGGAGCGCCACTCGGATTTTGGATTTCGGTCTCGCA GAAGGCGCCCCCAGGAGCCGGAGCGACCTCGGCGCGCCACTCGGATTTTGGATTTCGGTCTCGCA A C MIDN Ensembl:ENSG00000167470 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1248652..1250229 32194978 MeRIP-seq:(Medium) rs1342303862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559979 80322 RMVar_ID_80322 Human_SNP_ID_655345519 m1A Human chr19 + 1250387 1250387 1250387 GCGAGCTGGGCCCGGCGGCCGAGGCGGCGCCCATGAGCCTCGCCATCCACAGCACCACGGGCACC GCGAGCTGGGCCCGGCGGCCGAGGCGGCGCCCGTGAGCCTCGCCATCCACAGCACCACGGGCACC A G MIDN Ensembl:ENSG00000167470 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1250373..1250479 26863196 MeRIP-seq:(Medium) rs1209656447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4501605,Human_RBP_ID_9329348,Human_RBP_ID_22447117 80323 RMVar_ID_80323 Human_SNP_ID_655346124 m1A Human chr19 - 1251503 1251503 1251503 ACTCCGCGGAGACGACACAGGGACGCGGAAGCAGAGGCCGCGGGGGAGGGCTGTGCTTGTGTGGG ACTCCGCGGAGACGACACAGGGACGCGGAAGCGGAGGCCGCGGGGGAGGGCTGTGCTTGTGTGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1251492..1251590 26863196 MeRIP-seq:(Medium) rs1342667033 Functional Loss SNV dbSNP153 33..33 33 - - - 80324 RMVar_ID_80324 Human_SNP_ID_655347738 m1A Human chr19 - 1254393 1254393 1254393 GCGAGGGAGATGCAGGGGACGGGCTGGTGGGCACCGGGGGGACTCGGGCGGCACTGGACACCGGC GCGAGGGAGATGCAGGGGACGGGCTGGTGGGCCCCGGGGGGACTCGGGCGGCACTGGACACCGGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1254343..1254499 26863196 MeRIP-seq:(Medium) rs1283703268 Functional Loss SNV dbSNP153 33..33 33 - - - 80325 RMVar_ID_80325 Human_SNP_ID_655347757 m1A Human chr19 - 1254412 1254412 1254412 AAGGAGCCGGCTGTGATGGGCGAGGGAGATGCAGGGGACGGGCTGGTGGGCACCGGGGGGACTCG AAGGAGCCGGCTGTGATGGGCGAGGGAGATGCGGGGGACGGGCTGGTGGGCACCGGGGGGACTCG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1254312..1254985 26863196 MeRIP-seq:(Medium) rs933529976 Functional Loss SNV dbSNP153 33..33 33 - - - 80326 RMVar_ID_80326 Human_SNP_ID_655348004 m1A Human chr19 - 1254906 1254906 1254906 TGGCACTGCTGCTGGCCGTGGGGGAGCAGTCCATCTGCTGATGGGAGGAAGGGGCACATGAGCAC TGGCACTGCTGCTGGCCGTGGGGGAGCAGTCCGTCTGCTGATGGGAGGAAGGGGCACATGAGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1254895..1254972 26863196 MeRIP-seq:(Medium) rs767695604 Functional Loss SNV dbSNP153 33..33 33 - - - 80327 RMVar_ID_80327 Human_SNP_ID_655348043 m1A Human chr19 + 1254962 1254962 1254962 GCAGTGCCAGTCCTGGTGCCAGCACCACGTCTACCCCAGGGGCCAGCCCTGCCCCCCGCTCCCGA GCAGTGCCAGTCCTGGTGCCAGCACCACGTCTTCCCCAGGGGCCAGCCCTGCCCCCCGCTCCCGA A T MIDN Ensembl:ENSG00000167470 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1254951..1254975 26863196 MeRIP-seq:(Medium) rs762150212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513110 Human_Splice_Rec_1931498,Human_Splice_Rec_1931499,Human_Splice_Rec_1931510,Human_Splice_Rec_1931511 Human_miRNA_ID_2437199,Human_miRNA_ID_2464360,Human_miRNA_ID_2561213 RMVar_hsa_circ_109967,RMVar_hsa_circ_50030,RMVar_hsa_circ_118654,RMVar_hsa_circ_191028,RMVar_hsa_circ_191029 80328 RMVar_ID_80328 Human_SNP_ID_655348093 m1A Human chr19 - 1255063 1255063 1255063 ACACGTGAGCTCACACATGTGCTGTGACACCTACCAGAGAAGGTCCCTGAGAAGACCCCCGGGGC ACACGTGAGCTCACACATGTGCTGTGACACCTGCCAGAGAAGGTCCCTGAGAAGACCCCCGGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1255034..1255545 32194978 MeRIP-seq:(Medium) rs758171584 Functional Loss SNV dbSNP153 33..33 33 - - - 80329 RMVar_ID_80329 Human_SNP_ID_655348401 m1A Human chr19 + 1255596 1255585 1255597 CGCCCAGTGCTCCCCGGCCTCACCGGCCCCCGACCTGGCCCCCAGAACTACCTCCTGCGAGAAGC CGCCCAGTGCTCCCCGGCCTCA____________CTGGCCCCCAGAACTACCTCCTGCGAGAAGC ACCGGCCCCCGAC A MIDN Ensembl:ENSG00000167470 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1255432..1257137 26863196 MeRIP-seq:(Medium) rs990194924 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_27267741 Human_Splice_Rec_1931501,Human_Splice_Rec_1931513 Human_miRNA_ID_16260,Human_miRNA_ID_1285653,Human_miRNA_ID_2168854,Human_miRNA_ID_2663447,Human_miRNA_ID_2681903 RMVar_hsa_circ_109967,RMVar_hsa_circ_191029 80330 RMVar_ID_80330 Human_SNP_ID_655350041 m1A Human chr19 - 1259037 1259037 1259037 TTTCATACATGAAACTCACGCCAGGTGCCGGGACCCCCACAGCCCGACCCCCCGAGGGCGGGTAA TTTCATACATGAAACTCACGCCAGGTGCCGGGCCCCCCACAGCCCGACCCCCCGAGGGCGGGTAA T G lnc-CBARP-2,lnc-CBARP-2:2 RNACentral:URS00008B238D,RNACentral:URS0000EBCF7E lincRNA,lincRNA intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1258989..1259090 32194978 MeRIP-seq:(Medium) rs1469258242 Functional Loss SNV dbSNP153 33..33 33 - - - 80331 RMVar_ID_80331 Human_SNP_ID_655350943 m1A Human chr19 + 1261539 1261539 1261539 GGGGGCAACCGGGAAGTCAGTTGGTGGAGAAAAATCAAAGATGGGAGGAAAGGCGAGGCTGACAA GGGGGCAACCGGGAAGTCAGTTGGTGGAGAAATATCAAAGATGGGAGGAAAGGCGAGGCTGACAA A T CIRBP Ensembl:ENSG00000099622 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1261177..1262015 26863196 MeRIP-seq:(Medium) rs1298786903 Functional Loss SNV dbSNP153 33..33 33 - - - 80332 RMVar_ID_80332 Human_SNP_ID_655352611 m1A Human chr19 + 1266681 1266681 1266681 ATGGCGACGCCCCGCAGGGGAGGAGGCCCGGGAGGAGTATCAGGGTGCAGGAGGTGCGCGCCCCT ATGGCGACGCCCCGCAGGGGAGGAGGCCCGGGGGGAGTATCAGGGTGCAGGAGGTGCGCGCCCCT A G CIRBP Ensembl:ENSG00000099622 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1266669..1266751 26863196 MeRIP-seq:(Medium) rs916568770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582225 Human_Splice_Rec_1931555 80333 RMVar_ID_80333 Human_SNP_ID_655353599 m1A Human chr19 + 1269390 1269390 1269390 TCGTTGTGGTGCGCTGTCTTCCCGCTTGCGTCAGGGACCTGCCCGACTCAGTGGTGAGGGCCCTG TCGTTGTGGTGCGCTGTCTTCCCGCTTGCGTCGGGGACCTGCCCGACTCAGTGGTGAGGGCCCTG A G CIRBP Ensembl:ENSG00000099622 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1269326..1271057 26863196 MeRIP-seq:(Medium) rs1270711008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239391,Human_RBP_ID_513179,Human_RBP_ID_825707,Human_RBP_ID_906946,Human_RBP_ID_1554349,Human_RBP_ID_3953971,Human_RBP_ID_4501880,Human_RBP_ID_5320831,Human_RBP_ID_5442675,Human_RBP_ID_6720371,Human_RBP_ID_8255780,Human_RBP_ID_8477092,Human_RBP_ID_13369442,Human_RBP_ID_17915083,Human_RBP_ID_18420812,Human_RBP_ID_18440518,Human_RBP_ID_18722378,Human_RBP_ID_18993943 Human_Splice_Rec_1931625,Human_Splice_Rec_1931637,Human_Splice_Rec_1931647,Human_Splice_Rec_1931657,Human_Splice_Rec_1931669,Human_Splice_Rec_1931681,Human_Splice_Rec_1931691,Human_Splice_Rec_1931699,Human_Splice_Rec_1931709,Human_Splice_Rec_1931715,Human_Splice_Rec_1931727,Human_Splice_Rec_1931735,Human_Splice_Rec_1931743,Human_Splice_Rec_1931751,Human_Splice_Rec_1931757,Human_Splice_Rec_1931767,Human_Splice_Rec_1931775,Human_Splice_Rec_1931785,Human_Splice_Rec_1931795,Human_Splice_Rec_1931807,Human_Splice_Rec_1931821,Human_Splice_Rec_1931829,Human_Splice_Rec_1931841,Human_Splice_Rec_1931853,Human_Splice_Rec_1931859,Human_Splice_Rec_1931875 Human_miRNA_ID_3002085 RMVar_hsa_circ_191030,RMVar_hsa_circ_126068,RMVar_hsa_circ_340609 80334 RMVar_ID_80334 Human_SNP_ID_655353609 m1A Human chr19 + 1269403 1269403 1269403 CTGTCTTCCCGCTTGCGTCAGGGACCTGCCCGACTCAGTGGTGAGGGCCCTGGCTGCACCGGCTC CTGTCTTCCCGCTTGCGTCAGGGACCTGCCCGGCTCAGTGGTGAGGGCCCTGGCTGCACCGGCTC A G CIRBP Ensembl:ENSG00000099622 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1269326..1269459 26863410 MeRIP-seq:(Medium) rs1324599121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239391,Human_RBP_ID_513180,Human_RBP_ID_906946,Human_RBP_ID_3953971,Human_RBP_ID_4557799,Human_RBP_ID_5320831,Human_RBP_ID_8477092,Human_RBP_ID_9084459,Human_RBP_ID_17915083,Human_RBP_ID_18420812,Human_RBP_ID_18993943,Human_RBP_ID_26759398 Human_Splice_Rec_1931625,Human_Splice_Rec_1931637,Human_Splice_Rec_1931647,Human_Splice_Rec_1931657,Human_Splice_Rec_1931669,Human_Splice_Rec_1931681,Human_Splice_Rec_1931691,Human_Splice_Rec_1931699,Human_Splice_Rec_1931709,Human_Splice_Rec_1931715,Human_Splice_Rec_1931727,Human_Splice_Rec_1931735,Human_Splice_Rec_1931743,Human_Splice_Rec_1931751,Human_Splice_Rec_1931757,Human_Splice_Rec_1931767,Human_Splice_Rec_1931775,Human_Splice_Rec_1931785,Human_Splice_Rec_1931795,Human_Splice_Rec_1931807,Human_Splice_Rec_1931821,Human_Splice_Rec_1931829,Human_Splice_Rec_1931841,Human_Splice_Rec_1931853,Human_Splice_Rec_1931859,Human_Splice_Rec_1931875 RMVar_hsa_circ_191030,RMVar_hsa_circ_126068,RMVar_hsa_circ_340609 80335 RMVar_ID_80335 Human_SNP_ID_655353610 m1A Human chr19 - 1269409 1269406 1269409 TCCTCGGAGCCGGTGCAGCCAGGGCCCTCACCACTGAGTCGGGCAGGTCCCTGACGCAAGCGGGA TCCTCGGAGCCGGTGCAGCCAGGGCCCTCACC___GAGTCGGGCAGGTCCCTGACGCAAGCGGGA CAGT C CIRBP-AS1 Ensembl:ENSG00000267493 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1269398..1270950 32194978 MeRIP-seq:(Medium) rs1285549922 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5587813 80336 RMVar_ID_80336 Human_SNP_ID_655354652 m1A Human chr19 - 1271409 1271409 1271409 CGGCCCCCACGGAAGAAGCCCCGGCCCCCGGCAGAGCCACCACGGTACCCACGGGATCGGTTGTC CGGCCCCCACGGAAGAAGCCCCGGCCCCCGGCTGAGCCACCACGGTACCCACGGGATCGGTTGTC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1271240..1271565 26863196 MeRIP-seq:(Medium) rs751383283 Functional Loss SNV dbSNP153 33..33 33 - - - 80337 RMVar_ID_80337 Human_SNP_ID_655355218 m1A Human chr19 - 1272358 1272358 1272358 AAGCAACAAGAGGCAGCTTCACCCCAGAGGCCAGACCAGGGCGCGGCCTGCGGCCGGGGAGCAAC AAGCAACAAGAGGCAGCTTCACCCCAGAGGCCGGACCAGGGCGCGGCCTGCGGCCGGGGAGCAAC T C lnc-CBARP-6 RNACentral:URS0000D58839 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1272356..1272528 26863196 MeRIP-seq:(Medium) rs747381780 Functional Loss SNV dbSNP153 33..33 33 - - - 80338 RMVar_ID_80338 Human_SNP_ID_655355226 m1A Human chr19 - 1272376 1272376 1272376 CACAGTGTAAAGGCACCGAAGCAACAAGAGGCAGCTTCACCCCAGAGGCCAGACCAGGGCGCGGC CACAGTGTAAAGGCACCGAAGCAACAAGAGGCGGCTTCACCCCAGAGGCCAGACCAGGGCGCGGC T C lnc-CBARP-6 RNACentral:URS0000D58839 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1271994..1272450 32194978 MeRIP-seq:(Medium) rs1413854445 Functional Loss SNV dbSNP153 33..33 33 - - - 80339 RMVar_ID_80339 Human_SNP_ID_655355443 m1A Human chr19 - 1272859 1272858 1272860 AAAAAAGCCACAGCTTGCTCAGCTTCCGACAAAGAGCGGATTCACAGTCCGTTCGATCTCAGAGA AAAAAAGCCACAGCTTGCTCAGCTTCCGACA__GAGCGGATTCACAGTCCGTTCGATCTCAGAGA CTT C lnc-CBARP-6 RNACentral:URS0000D58839 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1272808..1273070 26863196 MeRIP-seq:(Medium) rs775577337 Functional Loss DEL dbSNP153 32..33 33 - - - 80340 RMVar_ID_80340 Human_SNP_ID_655355594 m1A Human chr19 - 1273239 1273239 1273239 ACCCGCTGCTTCTCCACCTTCTCTCTCTGCTCAGGTCTGGCTGCAGGAGCCCGCAGCAAGGAGTG ACCCGCTGCTTCTCCACCTTCTCTCTCTGCTCGGGTCTGGCTGCAGGAGCCCGCAGCAAGGAGTG T C lnc-CBARP-6 RNACentral:URS0000D58839 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1273238..1273437 32194978 MeRIP-seq:(Medium) rs1185639266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17915109 80341 RMVar_ID_80341 Human_SNP_ID_655355628 m1A Human chr19 - 1273323 1273323 1273323 CCCCGCCTGGCTCCCCTACCCTGACCAGCGCCAGTCTGCTGGGCCTCCCTTTCTAGCTCTGCAGG CCCCGCCTGGCTCCCCTACCCTGACCAGCGCCTGTCTGCTGGGCCTCCCTTTCTAGCTCTGCAGG T A lnc-CBARP-6 RNACentral:URS0000D58839 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1273292..1273433 26863196 MeRIP-seq:(Medium) rs1339465052 Functional Loss SNV dbSNP153 33..33 33 - - - 80342 RMVar_ID_80342 Human_SNP_ID_655356795 m1A Human chr19 - 1275602 1275602 1275602 CCTCTTCGGCACCGCACGGCAGCGCCGCCAGCAGCAGCGCCAGCAGGAGCAGCAGCAGCGGCGGC CCTCTTCGGCACCGCACGGCAGCGCCGCCAGCGGCAGCGCCAGCAGGAGCAGCAGCAGCGGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1275551..1275800;chr19:1275551..1275769 26863196 MeRIP-seq:(Medium) rs545545504 Functional Loss SNV dbSNP153 33..33 33 - - - 80343 RMVar_ID_80343 Human_SNP_ID_655356907 m1A Human chr19 - 1275758 1275758 1275758 AGAAGCCCAGGATCACGTAGAAGGAGCGCGTCAGCGCCGAGCCCGACGCCCCCGGCGGACGCGTG AGAAGCCCAGGATCACGTAGAAGGAGCGCGTCGGCGCCGAGCCCGACGCCCCCGGCGGACGCGTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1275586..1275787 32194978 MeRIP-seq:(Medium) rs1373884757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4502123 80344 RMVar_ID_80344 Human_SNP_ID_655357122 m1A Human chr19 + 1276012 1276012 1276012 GGTCGTCACGTGGTGTGGGCGGTGCAGGGGCCACGGGACTCACCCGCTCTCCAGCCTGCGCCTGG GGTCGTCACGTGGTGTGGGCGGTGCAGGGGCCGCGGGACTCACCCGCTCTCCAGCCTGCGCCTGG A G FAM174C Ensembl:ENSG00000228300 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1276007..1276325 26863196 MeRIP-seq:(Medium) rs1250284898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582230,Human_RBP_ID_5374756,Human_RBP_ID_8195145,Human_RBP_ID_18488716,Human_RBP_ID_18944571,Human_RBP_ID_21977382,Human_RBP_ID_26784179 Human_Splice_Rec_1931923 RMVar_hsa_circ_114833,RMVar_hsa_circ_191038 80345 RMVar_ID_80345 Human_SNP_ID_655357125 m1A Human chr19 + 1276017 1276017 1276017 TCACGTGGTGTGGGCGGTGCAGGGGCCACGGGACTCACCCGCTCTCCAGCCTGCGCCTGGGGTTG TCACGTGGTGTGGGCGGTGCAGGGGCCACGGGGCTCACCCGCTCTCCAGCCTGCGCCTGGGGTTG A G FAM174C Ensembl:ENSG00000228300 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1276012..1276176 26863196 MeRIP-seq:(Medium) rs1180640515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582230,Human_RBP_ID_5374756,Human_RBP_ID_8195145,Human_RBP_ID_18488716,Human_RBP_ID_18944571,Human_RBP_ID_21977382,Human_RBP_ID_26784179 Human_Splice_Rec_1931923 RMVar_hsa_circ_114833,RMVar_hsa_circ_191038 80346 RMVar_ID_80346 Human_SNP_ID_655357219 m1A Human chr19 - 1276228 1276228 1276228 AGCAGAAAGGAAAATATCGGGACCCCACGGAAAGGCCTGGCGGCAGGCGGGAAGATGAGAACGAG AGCAGAAAGGAAAATATCGGGACCCCACGGAACGGCCTGGCGGCAGGCGGGAAGATGAGAACGAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1276225..1276325 26863196 MeRIP-seq:(Medium) rs1163215739 Functional Loss SNV dbSNP153 33..33 33 - - - 80347 RMVar_ID_80347 Human_SNP_ID_655359870 m1A Human chr19 - 1282745 1282745 1282745 CCATTCCCAGCTCACCCTCCTCCCTCCTCCCCAGCTCCCATCCTTCCCATTCTCCTCTCTTCACA CCATTCCCAGCTCACCCTCCTCCCTCCTCCCCCGCTCCCATCCTTCCCATTCTCCTCTCTTCACA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1282736..1282846 26863196 MeRIP-seq:(Medium) rs1242243902 Functional Loss SNV dbSNP153 33..33 33 - - - 80348 RMVar_ID_80348 Human_SNP_ID_655360958 m1A Human chr19 + 1286117 1286108 1286117 CGGCGGCGGCGGCGGCGGCGGAGGAGGCGGAGAAGGCTGGCAGGCGGCGGCCGGGAGAGCGAGCG CGGCGGCGGCGGCGGCGGCGGAGG_________AGGCTGGCAGGCGGCGGCCGGGAGAGCGAGCG GAGGCGGAGA G EFNA2 Ensembl:ENSG00000099617 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1286112..1286209 26863196 MeRIP-seq:(Medium) rs1464594904 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4556979,Human_RBP_ID_5239488,Human_RBP_ID_22719581,Human_RBP_ID_26784727 80349 RMVar_ID_80349 Human_SNP_ID_655364008 m1A Human chr19 - 1295775 1295775 1295775 GCGTGAAGAGCTGGAACTTCTCCGAGAACTTGAGCGGCCCCCCGGGCGCCGCGGGCCGGTTGCAC GCGTGAAGAGCTGGAACTTCTCCGAGAACTTGCGCGGCCCCCCGGGCGCCGCGGGCCGGTTGCAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1286253..1295789 32194978 MeRIP-seq:(Medium) rs748462948 Functional Loss SNV dbSNP153 33..33 33 - - - 80350 RMVar_ID_80350 Human_SNP_ID_655375921 m1A Human chr19 + 1330345 1330345 1330345 TATTTTTAGTAGAGATGGGGTTTCATCGTGTTAGCCAGGATGAGTCTCGATCTCCTGACCTCGTG TATTTTTAGTAGAGATGGGGTTTCATCGTGTTCGCCAGGATGAGTCTCGATCTCCTGACCTCGTG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:1330338..1330422 26863410 MeRIP-seq:(Medium) rs970488598 Functional Loss SNV dbSNP153 33..33 33 - - - 80351 RMVar_ID_80351 Human_SNP_ID_655384116 m1A Human chr19 + 1355016 1354992 1355016 AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG AGCGGCGGC________________________GGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG CGGCGGCGGCGGCGGCGGTGGCGGA C PWWP3A Ensembl:ENSG00000160953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1354991..1355088;chr19:1355007..1355181 26863196 MeRIP-seq:(Medium) rs1349101586 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_4503915 Human_Splice_Rec_1931945,Human_Splice_Rec_1931949,Human_Splice_Rec_1931957 80352 RMVar_ID_80352 Human_SNP_ID_655384122 m1A Human chr19 + 1355016 1354998 1355016 AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG AGCGGCGGCGGCGGC__________________GGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG CGGCGGCGGCGGTGGCGGA C PWWP3A Ensembl:ENSG00000160953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1354991..1355088;chr19:1355007..1355181 26863196 MeRIP-seq:(Medium) rs930951416 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_4503915 Human_Splice_Rec_1931945,Human_Splice_Rec_1931949,Human_Splice_Rec_1931957 80353 RMVar_ID_80353 Human_SNP_ID_655384126 m1A Human chr19 + 1355016 1355001 1355016 AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG AGCGGCGGCGGCGGCGGC_______________GGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG CGGCGGCGGTGGCGGA C PWWP3A Ensembl:ENSG00000160953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1354991..1355088;chr19:1355007..1355181 26863196 MeRIP-seq:(Medium) rs1048503488 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_4503915 Human_Splice_Rec_1931945,Human_Splice_Rec_1931949,Human_Splice_Rec_1931957 80354 RMVar_ID_80354 Human_SNP_ID_655384131 m1A Human chr19 + 1355016 1355004 1355016 AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG AGCGGCGGCGGCGGCGGCGGC____________GGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG CGGCGGTGGCGGA C PWWP3A Ensembl:ENSG00000160953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1354991..1355088;chr19:1355007..1355181 26863196 MeRIP-seq:(Medium) rs761277194 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4503915 Human_Splice_Rec_1931945,Human_Splice_Rec_1931949,Human_Splice_Rec_1931957 80355 RMVar_ID_80355 Human_SNP_ID_655384149 m1A Human chr19 + 1355016 1355016 1355016 AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG AGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCG A C PWWP3A Ensembl:ENSG00000160953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1354991..1355088;chr19:1355007..1355181 26863196 MeRIP-seq:(Medium) rs1184006116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4503915 Human_Splice_Rec_1931945,Human_Splice_Rec_1931949,Human_Splice_Rec_1931957 80356 RMVar_ID_80356 Human_SNP_ID_655384167 m1A Human chr19 + 1355040 1355039 1355040 GGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCGGTTGGCGGGCGGGTCCTCCGCTGT GGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGG_CGGCAGCGGTTGGCGGGCGGGTCCTCCGCTGT GA G PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:1355030..1355121;chr19:1355033..1355145 26863410,26863196 MeRIP-seq:(Medium) rs1349134312 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1931963 80357 RMVar_ID_80357 Human_SNP_ID_655384168 m1A Human chr19 + 1355040 1355040 1355040 GGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGACGGCAGCGGTTGGCGGGCGGGTCCTCCGCTGT GGTGGCGGAGGCGGTGAGCGCGGGCGGCGCGGTCGGCAGCGGTTGGCGGGCGGGTCCTCCGCTGT A T PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:1355030..1355121;chr19:1355033..1355145 26863410,26863196 MeRIP-seq:(Medium) rs1466801979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1931963 80358 RMVar_ID_80358 Human_SNP_ID_655390568 m1A Human chr19 + 1373048 1373048 1373048 CACTTGGGGCCAGTTGGGCAGTGCCTGCTGCTATTGAGCCCCGTGCCCTCTCACAGGCCATCATC CACTTGGGGCCAGTTGGGCAGTGCCTGCTGCTGTTGAGCCCCGTGCCCTCTCACAGGCCATCATC A G PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1373045..1373180 26863196 MeRIP-seq:(Medium) rs1437599807 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22663363 RMVar_hsa_circ_306112,RMVar_hsa_circ_191044,RMVar_hsa_circ_356391,RMVar_hsa_circ_191047 80359 RMVar_ID_80359 Human_SNP_ID_655392352 m1A Human chr19 + 1376599 1376599 1376599 CCGTCGGTGAGGGAGCAGCCGGCTGTGCTGTCAGCGGGGCCTGGCGGTGGAAGCGCCTCCAGTGT CCGTCGGTGAGGGAGCAGCCGGCTGTGCTGTCGGCGGGGCCTGGCGGTGGAAGCGCCTCCAGTGT A G PWWP3A Ensembl:ENSG00000160953 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1376556..1376639 26863196 MeRIP-seq:(Medium) rs1472322739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526734,Human_RBP_ID_18995763,Human_RBP_ID_23783341 Human_Splice_Rec_1932016,Human_Splice_Rec_1932048,Human_Splice_Rec_1932074,Human_Splice_Rec_1932100,Human_Splice_Rec_1932136,Human_Splice_Rec_1932138,Human_Splice_Rec_1932140,Human_Splice_Rec_1932142 80360 RMVar_ID_80360 Human_SNP_ID_655394895 m1A Human chr19 - 1383646 1383645 1383647 CACTCATTTTCTTGTTATTCCAGGAGGGCAAAAGTCACCACGCGTCCCTGGGTGGGCTCGAACCA CACTCATTTTCTTGTTATTCCAGGAGGGCAA__GTCACCACGCGTCCCTGGGTGGGCTCGAACCA CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1383644..1383792 26863196 MeRIP-seq:(Medium) rs943660618 Functional Loss DEL dbSNP153 32..33 33 - - - 80361 RMVar_ID_80361 Human_SNP_ID_655394897 m1A Human chr19 - 1383646 1383646 1383646 CACTCATTTTCTTGTTATTCCAGGAGGGCAAAAGTCACCACGCGTCCCTGGGTGGGCTCGAACCA CACTCATTTTCTTGTTATTCCAGGAGGGCAAATGTCACCACGCGTCCCTGGGTGGGCTCGAACCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1383644..1383792 26863196 MeRIP-seq:(Medium) rs781319158 Functional Loss SNV dbSNP153 33..33 33 - - - 80362 RMVar_ID_80362 Human_SNP_ID_655394898 m1A Human chr19 - 1383646 1383646 1383646 CACTCATTTTCTTGTTATTCCAGGAGGGCAAAAGTCACCACGCGTCCCTGGGTGGGCTCGAACCA CACTCATTTTCTTGTTATTCCAGGAGGGCAAAGGTCACCACGCGTCCCTGGGTGGGCTCGAACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1383644..1383792 26863196 MeRIP-seq:(Medium) rs781319158 Functional Loss SNV dbSNP153 33..33 33 - - - 80363 RMVar_ID_80363 Human_SNP_ID_655394900 m1A Human chr19 - 1383648 1383648 1383648 GACACTCATTTTCTTGTTATTCCAGGAGGGCAAAAGTCACCACGCGTCCCTGGGTGGGCTCGAAC GACACTCATTTTCTTGTTATTCCAGGAGGGCAGAAGTCACCACGCGTCCCTGGGTGGGCTCGAAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1383645..1383772 26863196 MeRIP-seq:(Medium) rs902045467 Functional Loss SNV dbSNP153 33..33 33 - - - 80364 RMVar_ID_80364 Human_SNP_ID_655396536 m1A Human chr19 - 1388595 1388587 1388596 GGGGGTACGACCTCCCCCAGAAGGCCAGCTTCACCTGCTTGGGCCATCGGTGGCCACGCTCTGAT GGGGGTACGACCTCCCCCAGAAGGCCAGCTT_________GGGCCATCGGTGGCCACGCTCTGAT CAAGCAGGTG C AC005329.3 Ensembl:ENSG00000280486 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1388526..1388622 26863196 MeRIP-seq:(Medium) rs753037012 Functional Loss DEL dbSNP153 32..40 33 - - - 80365 RMVar_ID_80365 Human_SNP_ID_655396698 m1A Human chr19 + 1388882 1388882 1388882 CAAAGGCCAGAGCCGTGGCTCCCAAACCCAGCAGCCGGGGCGAGTATGTGGTGGCCAAGCTGGAT CAAAGGCCAGAGCCGTGGCTCCCAAACCCAGCGGCCGGGGCGAGTATGTGGTGGCCAAGCTGGAT A G NDUFS7 Ensembl:ENSG00000115286 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1388776..1388985;chr19:1388826..1388900 26863196 MeRIP-seq:(Medium) rs1393428572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513870,Human_RBP_ID_4557812,Human_RBP_ID_17656486,Human_RBP_ID_22447120 Human_Splice_Rec_1932154,Human_Splice_Rec_1932155,Human_Splice_Rec_1932165,Human_Splice_Rec_1932176,Human_Splice_Rec_1932177,Human_Splice_Rec_1932191,Human_Splice_Rec_1932200,Human_Splice_Rec_1932201,Human_Splice_Rec_1932210,Human_Splice_Rec_1932211,Human_Splice_Rec_1932224,Human_Splice_Rec_1932234,Human_Splice_Rec_1932235,Human_Splice_Rec_1932246,Human_Splice_Rec_1932247,Human_Splice_Rec_1932260,Human_Splice_Rec_1932261,Human_Splice_Rec_1932276,Human_Splice_Rec_1932277,Human_Splice_Rec_1932290,Human_Splice_Rec_1932291,Human_Splice_Rec_1932303,Human_Splice_Rec_1932314,Human_Splice_Rec_1932315,Human_Splice_Rec_1932326,Human_Splice_Rec_1932327,Human_Splice_Rec_1932336,Human_Splice_Rec_1932337,Human_Splice_Rec_1932346,Human_Splice_Rec_1932347,Human_Splice_Rec_1932358,Human_Splice_Rec_1932359 Human_miRNA_ID_1358306 80366 RMVar_ID_80366 Human_SNP_ID_655398595 m1A Human chr19 + 1393185 1393185 1393185 AAGGCGGGTGGGGATGGGGCGAGGCCTCGTGGAGGGAGGGTGGGCAGGCGGGTCTTCGGCACACT AAGGCGGGTGGGGATGGGGCGAGGCCTCGTGGGGGGAGGGTGGGCAGGCGGGTCTTCGGCACACT A G NDUFS7 Ensembl:ENSG00000115286 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1393182..1393380 26863196 MeRIP-seq:(Medium) rs1361486498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22663364 RMVar_hsa_circ_191048,RMVar_hsa_circ_118756,RMVar_hsa_circ_122573,RMVar_hsa_circ_191049 80367 RMVar_ID_80367 Human_SNP_ID_655399594 m1A Human chr19 + 1395487 1395487 1395487 GGAGCGGAGGCTGCAGATCTGGTACCGCAGGTAGCGCCGCCGCCGCCGCCGCCGGAGCCTGTCGC GGAGCGGAGGCTGCAGATCTGGTACCGCAGGTGGCGCCGCCGCCGCCGCCGCCGGAGCCTGTCGC A G NDUFS7 Ensembl:ENSG00000115286 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1395448..1395531 26863196 MeRIP-seq:(Medium) rs1261129142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513911,Human_RBP_ID_4562493,Human_RBP_ID_9328053,Human_RBP_ID_17655746,Human_RBP_ID_18191578,Human_RBP_ID_22448118,Human_RBP_ID_22533059 Human_Splice_Rec_1932186,Human_Splice_Rec_1932254,Human_Splice_Rec_1932268,Human_Splice_Rec_1932284,Human_Splice_Rec_1932296,Human_Splice_Rec_1932332 RMVar_hsa_circ_191048,RMVar_hsa_circ_118756 80368 RMVar_ID_80368 Human_SNP_ID_655399621 m1A Human chr19 + 1395510 1395504 1395510 ACCGCAGGTAGCGCCGCCGCCGCCGCCGCCGGAGCCTGTCGCCGTCCTGTCCCCAGCCTGCTTGT ACCGCAGGTAGCGCCGCCGCCGCCGCC______GCCTGTCGCCGTCCTGTCCCCAGCCTGCTTGT CGCCGGA C NDUFS7 Ensembl:ENSG00000115286 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1395337..1395600 26863196 MeRIP-seq:(Medium) rs751344869 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_239936,Human_RBP_ID_513911,Human_RBP_ID_771053,Human_RBP_ID_5116491,Human_RBP_ID_5144816,Human_RBP_ID_8477812,Human_RBP_ID_9328053,Human_RBP_ID_17655747,Human_RBP_ID_18191578,Human_RBP_ID_22447123,Human_RBP_ID_22533059,Human_RBP_ID_23783425 RMVar_hsa_circ_191048,RMVar_hsa_circ_118756 80369 RMVar_ID_80369 Human_SNP_ID_655400805 m1A Human chr19 - 1398977 1398977 1398977 GCTGAAGCCGGGGGGCGTCCTCACCTACTGCAACCTCACCTCCTGGGGGGAGCTGATGAAGTCCA GCTGAAGCCGGGGGGCGTCCTCACCTACTGCAGCCTCACCTCCTGGGGGGAGCTGATGAAGTCCA T C GAMT Ensembl:ENSG00000130005 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1398901..1401472 32194978 MeRIP-seq:(Medium) rs202199674 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22448120 Human_Splice_Rec_1932394,Human_Splice_Rec_1932395,Human_Splice_Rec_1932402,Human_Splice_Rec_1932403,Human_Splice_Rec_1932408,Human_Splice_Rec_1932409,Human_Splice_Rec_1932418,Human_Splice_Rec_1932424,Human_Splice_Rec_1932425 Human_miRNA_ID_2007721,Human_miRNA_ID_2007722,Human_miRNA_ID_2469868,Human_miRNA_ID_2469869,Human_miRNA_ID_2995088,Human_miRNA_ID_2995089 Clinvar_Rec_377 RMVar_hsa_circ_87000,RMVar_hsa_circ_27789,RMVar_hsa_circ_119993,RMVar_hsa_circ_191050,RMVar_hsa_circ_191051,RMVar_hsa_circ_351522 80370 RMVar_ID_80370 Human_SNP_ID_655400806 m1A Human chr19 - 1398977 1398977 1398977 GCTGAAGCCGGGGGGCGTCCTCACCTACTGCAACCTCACCTCCTGGGGGGAGCTGATGAAGTCCA GCTGAAGCCGGGGGGCGTCCTCACCTACTGCACCCTCACCTCCTGGGGGGAGCTGATGAAGTCCA T G GAMT Ensembl:ENSG00000130005 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1398901..1401472 32194978 MeRIP-seq:(Medium) rs202199674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22448120 Human_Splice_Rec_1932394,Human_Splice_Rec_1932395,Human_Splice_Rec_1932402,Human_Splice_Rec_1932403,Human_Splice_Rec_1932408,Human_Splice_Rec_1932409,Human_Splice_Rec_1932418,Human_Splice_Rec_1932424,Human_Splice_Rec_1932425 Human_miRNA_ID_2007721,Human_miRNA_ID_2007722,Human_miRNA_ID_2469868,Human_miRNA_ID_2469869,Human_miRNA_ID_2995088,Human_miRNA_ID_2995089 Clinvar_Rec_377 RMVar_hsa_circ_87000,RMVar_hsa_circ_27789,RMVar_hsa_circ_119993,RMVar_hsa_circ_191050,RMVar_hsa_circ_191051,RMVar_hsa_circ_351522 80371 RMVar_ID_80371 Human_SNP_ID_655401036 m1A Human chr19 - 1399508 1399508 1399508 TGACGGTCACTTTGATGGTGAGGGGTGAGGGGACGTATCACAGGGTGGGCCTCCCCAGCTCCAAT TGACGGTCACTTTGATGGTGAGGGGTGAGGGGGCGTATCACAGGGTGGGCCTCCCCAGCTCCAAT T C GAMT Ensembl:ENSG00000130005 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1399507..1399609 26863196 MeRIP-seq:(Medium) rs1381014508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19088438,Human_RBP_ID_21977391 Human_Splice_Rec_1932390,Human_Splice_Rec_1932398,Human_Splice_Rec_1932414,Human_Splice_Rec_1932420 RMVar_hsa_circ_87000,RMVar_hsa_circ_191050 80372 RMVar_ID_80372 Human_SNP_ID_655401738 m1A Human chr19 + 1401376 1401376 1401376 AGCGCTCCATCACCGGCTTGCCCAGGATGCGCAGGTGCGTGTCCGCTGCGTCGTAGGCCGCGGGC AGCGCTCCATCACCGGCTTGCCCAGGATGCGCGGGTGCGTGTCCGCTGCGTCGTAGGCCGCGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1401326..1401490 26863196 MeRIP-seq:(Medium) rs1366789503 Functional Loss SNV dbSNP153 33..33 33 - - - 80373 RMVar_ID_80373 Human_SNP_ID_655401754 m1A Human chr19 + 1401398 1401398 1401398 CAGGATGCGCAGGTGCGTGTCCGCTGCGTCGTAGGCCGCGGGCGCCGCCCCCCACGCGGGGCTGC CAGGATGCGCAGGTGCGTGTCCGCTGCGTCGTGGGCCGCGGGCGCCGCCCCCCACGCGGGGCTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1401359..1401486 26863196 MeRIP-seq:(Medium) rs200833152 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_378 80374 RMVar_ID_80374 Human_SNP_ID_655403857 m1A Human chr19 + 1407539 1407539 1407539 CCCTGGACCCGCCCCCGGAGACCCCGTGCGGGAGCGCGCCCGGGCGTGCGCAGGGGCGGCGGCGC CCCTGGACCCGCCCCCGGAGACCCCGTGCGGGTGCGCGCCCGGGCGTGCGCAGGGGCGGCGGCGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1407534..1407854 26863196 MeRIP-seq:(Medium) rs994515937 Functional Loss SNV dbSNP153 33..33 33 - - - 80375 RMVar_ID_80375 Human_SNP_ID_655405081 m1A Human chr19 - 1410755 1410755 1410755 CAGTTCCATGACCGTGTGCTGCCTTGGAAGCCAGCAGAACACAATGGCCTGGGCGCTCGAGGTGA CAGTTCCATGACCGTGTGCTGCCTTGGAAGCCGGCAGAACACAATGGCCTGGGCGCTCGAGGTGA T C lnc-GAMT-4 RNACentral:URS00008B901F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1410753..1411117;chr19:1410751..1411096 26863196 MeRIP-seq:(Medium) rs1048661074 Functional Loss SNV dbSNP153 33..33 33 - - - 80376 RMVar_ID_80376 Human_SNP_ID_655408018 m1A Human chr19 + 1419807 1419807 1419807 TCACCCCACGCACACACTCATGAAACCATCCCAACCGTCACGGCAGCGAGCACTCACCCCACGCA TCACCCCACGCACACACTCATGAAACCATCCCGACCGTCACGGCAGCGAGCACTCACCCCACGCA A G DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1419804..1419934 26863196 MeRIP-seq:(Medium) rs1212828228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_202987,Human_RBP_ID_9425058,Human_RBP_ID_13375805,Human_RBP_ID_24532727 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_331845,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_369637,RMVar_hsa_circ_107704,RMVar_hsa_circ_191054,RMVar_hsa_circ_191056,RMVar_hsa_circ_191057,RMVar_hsa_circ_191058,RMVar_hsa_circ_191055,RMVar_hsa_circ_85965,RMVar_hsa_circ_106290,RMVar_hsa_circ_121986,RMVar_hsa_circ_191059,RMVar_hsa_circ_191060,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_191061 80377 RMVar_ID_80377 Human_SNP_ID_655408019 m1A Human chr19 + 1419807 1419807 1419807 TCACCCCACGCACACACTCATGAAACCATCCCAACCGTCACGGCAGCGAGCACTCACCCCACGCA TCACCCCACGCACACACTCATGAAACCATCCCTACCGTCACGGCAGCGAGCACTCACCCCACGCA A T DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1419804..1419934 26863196 MeRIP-seq:(Medium) rs1212828228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_202987,Human_RBP_ID_9425058,Human_RBP_ID_13375805,Human_RBP_ID_24532727 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_331845,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_369637,RMVar_hsa_circ_107704,RMVar_hsa_circ_191054,RMVar_hsa_circ_191056,RMVar_hsa_circ_191057,RMVar_hsa_circ_191058,RMVar_hsa_circ_191055,RMVar_hsa_circ_85965,RMVar_hsa_circ_106290,RMVar_hsa_circ_121986,RMVar_hsa_circ_191059,RMVar_hsa_circ_191060,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_191061 80378 RMVar_ID_80378 Human_SNP_ID_655408457 m1A Human chr19 - 1421110 1421104 1421110 GAAGAAGGGAAGGATAGTTAGTTCACACGGGAACCCTCCAAACCCTCCCGCGAGCTGCGGAGGAC GAAGAAGGGAAGGATAGTTAGTTCACACGGGA______CAAACCCTCCCGCGAGCTGCGGAGGAC GGAGGGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1421106..1421291 26863196 MeRIP-seq:(Medium) rs1281175587 Functional Loss DEL dbSNP153 33..38 33 - - - 80379 RMVar_ID_80379 Human_SNP_ID_655408471 m1A Human chr19 + 1421128 1421128 1421128 GAGGGTTTGGAGGGTTCCCGTGTGAACTAACTATCCTTCCCTTCTTCAACAGCAGAAAGGACCCA GAGGGTTTGGAGGGTTCCCGTGTGAACTAACTGTCCTTCCCTTCTTCAACAGCAGAAAGGACCCA A G DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1421126..1421150 26863196 MeRIP-seq:(Medium) rs75293379 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_910024,Human_RBP_ID_1292185,Human_RBP_ID_8101429,Human_RBP_ID_18488825,Human_RBP_ID_22545259,Human_RBP_ID_22664303,Human_RBP_ID_22741950,Human_RBP_ID_25442244 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_331845,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_369637,RMVar_hsa_circ_107704,RMVar_hsa_circ_191054,RMVar_hsa_circ_191056,RMVar_hsa_circ_191057,RMVar_hsa_circ_191058,RMVar_hsa_circ_191055,RMVar_hsa_circ_85965,RMVar_hsa_circ_106290,RMVar_hsa_circ_121986,RMVar_hsa_circ_191059,RMVar_hsa_circ_191060,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_191061 80380 RMVar_ID_80380 Human_SNP_ID_655408494 m1A Human chr19 + 1421201 1421201 1421201 AACAGTAAATCAAATAAGATATTTGTCGGTGGAATTCCTCACAATTGTGGTGAGACAGAGCTCAG AACAGTAAATCAAATAAGATATTTGTCGGTGGGATTCCTCACAATTGTGGTGAGACAGAGCTCAG A G DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1421126..1421250 32194978 MeRIP-seq:(Medium) rs772537153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52727,Human_RBP_ID_514072,Human_RBP_ID_1013262,Human_RBP_ID_1187452,Human_RBP_ID_1555239,Human_RBP_ID_1880418,Human_RBP_ID_3563547,Human_RBP_ID_4562600,Human_RBP_ID_6722235,Human_RBP_ID_8477967,Human_RBP_ID_8829833,Human_RBP_ID_13375897,Human_RBP_ID_17694679,Human_RBP_ID_17915727,Human_RBP_ID_18723146,Human_RBP_ID_18993969,Human_RBP_ID_22230105,Human_RBP_ID_22501741,Human_RBP_ID_22809440,Human_RBP_ID_22967198,Human_RBP_ID_23814105,Human_RBP_ID_26983652 Human_Splice_Rec_1932434,Human_Splice_Rec_1932435,Human_Splice_Rec_1932458,Human_Splice_Rec_1932459,Human_Splice_Rec_1932480,Human_Splice_Rec_1932481,Human_Splice_Rec_1932502,Human_Splice_Rec_1932503,Human_Splice_Rec_1932514,Human_Splice_Rec_1932515,Human_Splice_Rec_1932534,Human_Splice_Rec_1932535,Human_Splice_Rec_1932560,Human_Splice_Rec_1932566,Human_Splice_Rec_1932567 Human_miRNA_ID_2172466 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_331845,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_369637,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191056,RMVar_hsa_circ_191057,RMVar_hsa_circ_191055,RMVar_hsa_circ_106290,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_191061,RMVar_hsa_circ_126606,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063 80381 RMVar_ID_80381 Human_SNP_ID_655409458 m1A Human chr19 + 1424085 1424085 1424085 TTCTGAGACGGGTCTGTGTCCCCCTCCCCGCCACCTCCTCCCTCTTCCTCTCCACTGACTGAAGG TTCTGAGACGGGTCTGTGTCCCCCTCCCCGCCCCCTCCTCCCTCTTCCTCTCCACTGACTGAAGG A C DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1424076..1424215 26863196 MeRIP-seq:(Medium) rs1306780973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130059,Human_RBP_ID_13376215,Human_RBP_ID_17081501,Human_RBP_ID_18488833,Human_RBP_ID_18944597,Human_RBP_ID_20356420,Human_RBP_ID_22809478,Human_RBP_ID_27473260 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_191064 80382 RMVar_ID_80382 Human_SNP_ID_655409658 m1A Human chr19 + 1424480 1424480 1424480 AACCACAGTGACCTTTGTCCCCTCACAGTCTGAGCTGCCCTTTCTGCCCCGTTTCCATCTTTCCC AACCACAGTGACCTTTGTCCCCTCACAGTCTGGGCTGCCCTTTCTGCCCCGTTTCCATCTTTCCC A G DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1424477..1424547 26863196 MeRIP-seq:(Medium) rs1259702669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514125,Human_RBP_ID_1187493,Human_RBP_ID_2557174,Human_RBP_ID_3563584,Human_RBP_ID_5130062,Human_RBP_ID_8478036,Human_RBP_ID_13376250,Human_RBP_ID_17081504,Human_RBP_ID_18944600,Human_RBP_ID_20356448,Human_RBP_ID_22967240,Human_RBP_ID_23783700 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_191064 80383 RMVar_ID_80383 Human_SNP_ID_655409697 m1A Human chr19 + 1424598 1424598 1424598 GGCCCCTGTCTCTTCAGCTTGAGAGGCCCCACAGTAGGCTGCTCCTTCCGGGGGCCGTTGCCTGT GGCCCCTGTCTCTTCAGCTTGAGAGGCCCCACGGTAGGCTGCTCCTTCCGGGGGCCGTTGCCTGT A G DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1424590..1424744 26863196 MeRIP-seq:(Medium) rs376685101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3579993,Human_RBP_ID_5130062,Human_RBP_ID_6722360,Human_RBP_ID_8478038,Human_RBP_ID_13376300,Human_RBP_ID_20356450,Human_RBP_ID_22741952,Human_RBP_ID_22809486 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_191064 80384 RMVar_ID_80384 Human_SNP_ID_655409698 m1A Human chr19 + 1424598 1424598 1424598 GGCCCCTGTCTCTTCAGCTTGAGAGGCCCCACAGTAGGCTGCTCCTTCCGGGGGCCGTTGCCTGT GGCCCCTGTCTCTTCAGCTTGAGAGGCCCCACTGTAGGCTGCTCCTTCCGGGGGCCGTTGCCTGT A T DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1424590..1424744 26863196 MeRIP-seq:(Medium) rs376685101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3579993,Human_RBP_ID_5130062,Human_RBP_ID_6722360,Human_RBP_ID_8478038,Human_RBP_ID_13376300,Human_RBP_ID_20356450,Human_RBP_ID_22741952,Human_RBP_ID_22809486 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_191064 80385 RMVar_ID_80385 Human_SNP_ID_655410903 m1A Human chr19 + 1428894 1428894 1428894 GCCTCGGGACAGCAAGAGCCAAGCGCCGGGACAGCCAGGTGCCAGCCAGTGGGGGAGCCGGGTTG GCCTCGGGACAGCAAGAGCCAAGCGCCGGGACGGCCAGGTGCCAGCCAGTGGGGGAGCCGGGTTG A G DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs751568758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52737,Human_RBP_ID_6722588,Human_RBP_ID_13376717,Human_RBP_ID_17694689,Human_RBP_ID_17915824,Human_RBP_ID_18995779,Human_RBP_ID_22661529,Human_RBP_ID_26983828 Human_Splice_Rec_1932440,Human_Splice_Rec_1932464,Human_Splice_Rec_1932486,Human_Splice_Rec_1932506,Human_Splice_Rec_1932520,Human_Splice_Rec_1932540,Human_Splice_Rec_1932570 Human_miRNA_ID_794292,Human_miRNA_ID_2333187,Human_miRNA_ID_2966269,Human_miRNA_ID_2966270 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_36234,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066 80386 RMVar_ID_80386 Human_SNP_ID_655410905 m1A Human chr19 + 1428898 1428898 1428898 CGGGACAGCAAGAGCCAAGCGCCGGGACAGCCAGGTGCCAGCCAGTGGGGGAGCCGGGTTGTGCC CGGGACAGCAAGAGCCAAGCGCCGGGACAGCCGGGTGCCAGCCAGTGGGGGAGCCGGGTTGTGCC A G DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1428791..1429034 26863196 MeRIP-seq:(Medium) rs759678699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52737,Human_RBP_ID_6722588,Human_RBP_ID_13376719,Human_RBP_ID_17694689,Human_RBP_ID_17915824,Human_RBP_ID_18995779,Human_RBP_ID_22661529,Human_RBP_ID_26983828 Human_Splice_Rec_1932440,Human_Splice_Rec_1932441,Human_Splice_Rec_1932464,Human_Splice_Rec_1932465,Human_Splice_Rec_1932486,Human_Splice_Rec_1932487,Human_Splice_Rec_1932506,Human_Splice_Rec_1932520,Human_Splice_Rec_1932521,Human_Splice_Rec_1932540,Human_Splice_Rec_1932541,Human_Splice_Rec_1932570,Human_Splice_Rec_1932571,Human_Splice_Rec_1932579 Human_miRNA_ID_794292,Human_miRNA_ID_2333187,Human_miRNA_ID_2966269,Human_miRNA_ID_2966270 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_36234,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066 80387 RMVar_ID_80387 Human_SNP_ID_655410906 m1A Human chr19 + 1428898 1428898 1428898 CGGGACAGCAAGAGCCAAGCGCCGGGACAGCCAGGTGCCAGCCAGTGGGGGAGCCGGGTTGTGCC CGGGACAGCAAGAGCCAAGCGCCGGGACAGCCTGGTGCCAGCCAGTGGGGGAGCCGGGTTGTGCC A T DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1428791..1429034 26863196 MeRIP-seq:(Medium) rs759678699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52737,Human_RBP_ID_6722588,Human_RBP_ID_13376719,Human_RBP_ID_17694689,Human_RBP_ID_17915824,Human_RBP_ID_18995779,Human_RBP_ID_22661529,Human_RBP_ID_26983828 Human_Splice_Rec_1932440,Human_Splice_Rec_1932441,Human_Splice_Rec_1932464,Human_Splice_Rec_1932465,Human_Splice_Rec_1932486,Human_Splice_Rec_1932487,Human_Splice_Rec_1932506,Human_Splice_Rec_1932520,Human_Splice_Rec_1932521,Human_Splice_Rec_1932540,Human_Splice_Rec_1932541,Human_Splice_Rec_1932570,Human_Splice_Rec_1932571,Human_Splice_Rec_1932579 Human_miRNA_ID_794292,Human_miRNA_ID_2333187,Human_miRNA_ID_2966269,Human_miRNA_ID_2966270 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_36234,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066 80388 RMVar_ID_80388 Human_SNP_ID_655410926 m1A Human chr19 + 1428952 1428952 1428952 CGGGTTGTGCCCAACGCTGCCAATGGCTGGGCAGGCCAGCCCCCGCCCACGTGGCAGCAAGGATA CGGGTTGTGCCCAACGCTGCCAATGGCTGGGCGGGCCAGCCCCCGCCCACGTGGCAGCAAGGATA A G DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1403926901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514236,Human_RBP_ID_770034,Human_RBP_ID_9084690,Human_RBP_ID_9379969,Human_RBP_ID_18165339,Human_RBP_ID_18723307,Human_RBP_ID_18995780 Human_Splice_Rec_1932441,Human_Splice_Rec_1932465,Human_Splice_Rec_1932487,Human_Splice_Rec_1932521,Human_Splice_Rec_1932541,Human_Splice_Rec_1932571,Human_Splice_Rec_1932579 Human_miRNA_ID_2147292,Human_miRNA_ID_2988719,Human_miRNA_ID_3022418 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_36234,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066 80389 RMVar_ID_80389 Human_SNP_ID_655411437 m1A Human chr19 + 1430285 1430285 1430285 AGCCCCCCCGCCACCCCCACCGTTCACCTCCTACATCGTGTCCACCCCTCCTGGAGGCTTTCCCC AGCCCCCCCGCCACCCCCACCGTTCACCTCCTTCATCGTGTCCACCCCTCCTGGAGGCTTTCCCC A T DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1430276..1430463 26863196 MeRIP-seq:(Medium) rs1294542593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52738,Human_RBP_ID_3955796,Human_RBP_ID_6722598,Human_RBP_ID_18995781,Human_RBP_ID_22809539,Human_RBP_ID_25385999,Human_RBP_ID_26474559 Human_Splice_Rec_1932444,Human_Splice_Rec_1932445,Human_Splice_Rec_1932468,Human_Splice_Rec_1932469,Human_Splice_Rec_1932490,Human_Splice_Rec_1932491,Human_Splice_Rec_1932524,Human_Splice_Rec_1932525,Human_Splice_Rec_1932544,Human_Splice_Rec_1932545,Human_Splice_Rec_1932574,Human_Splice_Rec_1932575,Human_Splice_Rec_1932582,Human_Splice_Rec_1932583 Human_miRNA_ID_2153831,Human_miRNA_ID_2801707,Human_miRNA_ID_3009839 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_93413,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066,RMVar_hsa_circ_108515,RMVar_hsa_circ_111294,RMVar_hsa_circ_191067,RMVar_hsa_circ_191068,RMVar_hsa_circ_191069 80390 RMVar_ID_80390 Human_SNP_ID_655411460 m1A Human chr19 + 1430324 1430324 1430324 GTCCACCCCTCCTGGAGGCTTTCCCCCTCCCCAGGGCTTCCCTCAGGGCTACGGTGCCCCGCCAC GTCCACCCCTCCTGGAGGCTTTCCCCCTCCCCCGGGCTTCCCTCAGGGCTACGGTGCCCCGCCAC A C DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1430276..1430375 26863196 MeRIP-seq:(Medium) rs1419440873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239147,Human_RBP_ID_514244,Human_RBP_ID_3953989,Human_RBP_ID_4505246,Human_RBP_ID_6722599,Human_RBP_ID_13376829,Human_RBP_ID_17915828,Human_RBP_ID_18723314,Human_RBP_ID_18995781,Human_RBP_ID_23783837 Human_Splice_Rec_1932445,Human_Splice_Rec_1932469,Human_Splice_Rec_1932491,Human_Splice_Rec_1932525,Human_Splice_Rec_1932545,Human_Splice_Rec_1932575,Human_Splice_Rec_1932583 Human_miRNA_ID_1973792,Human_miRNA_ID_1975970,Human_miRNA_ID_2368173,Human_miRNA_ID_2613760,Human_miRNA_ID_3004783,Human_miRNA_ID_3015957 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_93413,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066,RMVar_hsa_circ_108515,RMVar_hsa_circ_111294,RMVar_hsa_circ_191067,RMVar_hsa_circ_191068,RMVar_hsa_circ_191069 80391 RMVar_ID_80391 Human_SNP_ID_655412707 m1A Human chr19 - 1433742 1433742 1433742 CGCAGCCCGGCGGGGCTGGAGAATAGGAACCCAGGCCTGGCAAGAGACGAGACCAGGGTGACCAA CGCAGCCCGGCGGGGCTGGAGAATAGGAACCCGGGCCTGGCAAGAGACGAGACCAGGGTGACCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1433740..1433827 26863196 MeRIP-seq:(Medium) rs1347167555 Functional Loss SNV dbSNP153 33..33 33 - - - 80392 RMVar_ID_80392 Human_SNP_ID_655413178 m1A Human chr19 - 1434968 1434968 1434968 GCCACTTTGCCGCCAAGTTTGTGATTGTCACGAGTTCACAAGTTTGGAATCCTGGGTCTGGGCCG GCCACTTTGCCGCCAAGTTTGTGATTGTCACGGGTTCACAAGTTTGGAATCCTGGGTCTGGGCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1434800..1435025 26863196 MeRIP-seq:(Medium) rs529117866 Functional Loss SNV dbSNP153 33..33 33 - - - 80393 RMVar_ID_80393 Human_SNP_ID_655413183 m1A Human chr19 - 1434971 1434971 1434971 GTCGCCACTTTGCCGCCAAGTTTGTGATTGTCACGAGTTCACAAGTTTGGAATCCTGGGTCTGGG GTCGCCACTTTGCCGCCAAGTTTGTGATTGTCTCGAGTTCACAAGTTTGGAATCCTGGGTCTGGG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:1434726..1435079 26863196 MeRIP-seq:(Medium) rs946061936 Functional Loss SNV dbSNP153 33..33 33 - - - 80394 RMVar_ID_80394 Human_SNP_ID_655413314 m1A Human chr19 + 1435263 1435262 1435263 TTTACGGTATATTGTAAACTTTTATGTTAAAGAAAAAATATACATTTACAAATTGTGAGATTTTT TTTACGGTATATTGTAAACTTTTATGTTAAAG_AAAAATATACATTTACAAATTGTGAGATTTTT GA G DAZAP1 Ensembl:ENSG00000071626 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1440600215 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_514267,Human_RBP_ID_1013310,Human_RBP_ID_1292225,Human_RBP_ID_1372031,Human_RBP_ID_1555505,Human_RBP_ID_1880508,Human_RBP_ID_2557243,Human_RBP_ID_3563648,Human_RBP_ID_6722657,Human_RBP_ID_17266820,Human_RBP_ID_17382210,Human_RBP_ID_17497961,Human_RBP_ID_17915844,Human_RBP_ID_18301690,Human_RBP_ID_18723349,Human_RBP_ID_22501765,Human_RBP_ID_24483669,Human_RBP_ID_26465069,Human_RBP_ID_26651240,Human_RBP_ID_27674884 RMVar_hsa_circ_101096,RMVar_hsa_circ_191053,RMVar_hsa_circ_126606,RMVar_hsa_circ_191063,RMVar_hsa_circ_76519,RMVar_hsa_circ_191066,RMVar_hsa_circ_108515,RMVar_hsa_circ_111294,RMVar_hsa_circ_191067,RMVar_hsa_circ_87866,RMVar_hsa_circ_191069,RMVar_hsa_circ_90781,RMVar_hsa_circ_191070,RMVar_hsa_circ_191071 80395 RMVar_ID_80395 Human_SNP_ID_655414617 m1A Human chr19 + 1438834 1438834 1438834 CACAGGCAGAAGTAGAGCAGAAGAAGAAGCGGACCTTCCGCAAGTTCACCTACCGCGGCGTGGAC CACAGGCAGAAGTAGAGCAGAAGAAGAAGCGGGCCTTCCGCAAGTTCACCTACCGCGGCGTGGAC A G RPS15 Ensembl:ENSG00000115268 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1438801..1438850 26863196 MeRIP-seq:(Medium) rs757963954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239923,Human_RBP_ID_514290,Human_RBP_ID_4562721,Human_RBP_ID_9084704,Human_RBP_ID_18723361,Human_RBP_ID_24545545,Human_RBP_ID_26814811,Human_RBP_ID_27268795 Human_Splice_Rec_1932588,Human_Splice_Rec_1932589,Human_Splice_Rec_1932594,Human_Splice_Rec_1932595,Human_Splice_Rec_1932600,Human_Splice_Rec_1932601,Human_Splice_Rec_1932606,Human_Splice_Rec_1932607,Human_Splice_Rec_1932611,Human_Splice_Rec_1932616,Human_Splice_Rec_1932617,Human_Splice_Rec_1932622,Human_Splice_Rec_1932623,Human_Splice_Rec_1932628,Human_Splice_Rec_1932629,Human_Splice_Rec_1932636,Human_Splice_Rec_1932637,Human_Splice_Rec_1932642,Human_Splice_Rec_1932646,Human_Splice_Rec_1932647,Human_Splice_Rec_1932650,Human_Splice_Rec_1932651,Human_Splice_Rec_1932656,Human_Splice_Rec_1932657 Human_miRNA_ID_2728314 RMVar_hsa_circ_107244,RMVar_hsa_circ_96325,RMVar_hsa_circ_191072,RMVar_hsa_circ_191073 80396 RMVar_ID_80396 Human_SNP_ID_655415093 m1A Human chr19 + 1440126 1440126 1440126 CCTGCTGAAGCGCCTGCGCAAGGCCAAGAAGGAGGCGCCGCCCATGGAGAAGCCGGAAGTGGTGA CCTGCTGAAGCGCCTGCGCAAGGCCAAGAAGGGGGCGCCGCCCATGGAGAAGCCGGAAGTGGTGA A G RPS15 Ensembl:ENSG00000115268 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1440101..1440125 26863196 MeRIP-seq:(Medium) rs1273622289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239924,Human_RBP_ID_514303,Human_RBP_ID_769646,Human_RBP_ID_825153,Human_RBP_ID_4562727,Human_RBP_ID_5117216,Human_RBP_ID_9329382,Human_RBP_ID_18191605 RMVar_hsa_circ_107244,RMVar_hsa_circ_96325,RMVar_hsa_circ_191072,RMVar_hsa_circ_191073,RMVar_hsa_circ_4053,RMVar_hsa_circ_100367,RMVar_hsa_circ_191075 80397 RMVar_ID_80397 Human_SNP_ID_655415108 m1A Human chr19 + 1440151 1440151 1440151 AAGAAGGAGGCGCCGCCCATGGAGAAGCCGGAAGTGGTGAAGACGCACCTGCGGGACATGATCAT AAGAAGGAGGCGCCGCCCATGGAGAAGCCGGATGTGGTGAAGACGCACCTGCGGGACATGATCAT A T RPS15 Ensembl:ENSG00000115268 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1440126..1440246 32194978 MeRIP-seq:(Medium) rs1467300522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239924,Human_RBP_ID_514303,Human_RBP_ID_769646,Human_RBP_ID_825153,Human_RBP_ID_5117216,Human_RBP_ID_9329382,Human_RBP_ID_18191605,Human_RBP_ID_22449116 Human_Splice_Rec_1932625 Human_miRNA_ID_2172467 RMVar_hsa_circ_107244,RMVar_hsa_circ_96325,RMVar_hsa_circ_191072,RMVar_hsa_circ_191073,RMVar_hsa_circ_4053,RMVar_hsa_circ_100367,RMVar_hsa_circ_191075 80398 RMVar_ID_80398 Human_SNP_ID_655415226 m1A Human chr19 - 1440408 1440408 1440408 GAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCATGCTTTACGGGCTTGTAGGTGATGGAGAACTC GAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCGTGCTTTACGGGCTTGTAGGTGATGGAGAACTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:1440362..1440456;chr19:1440220..1440500;chr19:1440376..1440475;chr19:1440361..1440450;chr19:1440344..1440475 26863196,26863410,26863196,26863196,32194978,32194978 MeRIP-seq:(Medium) rs767434466 Functional Loss SNV dbSNP153 33..33 33 - - - 80399 RMVar_ID_80399 Human_SNP_ID_655415241 m1A Human chr19 - 1440439 1440439 1440439 GCTGAGCCATTACTTGAGAGGGATGAAGCGGGAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCAT GCTGAGCCATTACTTGAGAGGGATGAAGCGGGTGGAGTGGGTGGCCCCGATGCCGGGCCGGCCAT T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1440277..1440443 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 80400 RMVar_ID_80400 Human_SNP_ID_655415242 m1A Human chr19 - 1440439 1440439 1440439 GCTGAGCCATTACTTGAGAGGGATGAAGCGGGAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCAT GCTGAGCCATTACTTGAGAGGGATGAAGCGGGGGGAGTGGGTGGCCCCGATGCCGGGCCGGCCAT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1440277..1440443 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 80401 RMVar_ID_80401 Human_SNP_ID_655422292 m1A Human chr19 - 1459390 1459390 1459390 CCTGTGCACACGATGGGATGTCACGCAGCCTCAGAAGGGAGCCAGGCTTTGGCCGGGTGTGGTGG CCTGTGCACACGATGGGATGTCACGCAGCCTCTGAAGGGAGCCAGGCTTTGGCCGGGTGTGGTGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1459388..1459541 26863196 MeRIP-seq:(Medium) rs189527382 Functional Loss SNV dbSNP153 33..33 33 - - - 80402 RMVar_ID_80402 Human_SNP_ID_655422470 m1A Human chr19 + 1459941 1459941 1459941 AGGCCCAGTGGCTGGAGGAAGCGTGAGCCAGGACCGAGGGCTGACAGGAGGCGGGGGTGGCAGTC AGGCCCAGTGGCTGGAGGAAGCGTGAGCCAGGGCCGAGGGCTGACAGGAGGCGGGGGTGGCAGTC A G APC2 Ensembl:ENSG00000115266 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1459891..1460120 26863196 MeRIP-seq:(Medium) rs1209878492 Functional Loss SNV dbSNP153 33..33 33 - - - 80403 RMVar_ID_80403 Human_SNP_ID_655426136 m1A Human chr19 + 1467959 1467959 1467959 GCAGGGCCGGAAGGAGGCCCCTGCCCCGTCCAAGGCTGCACCAGCTGCCCCGCCGCCCGCCCGGA GCAGGGCCGGAAGGAGGCCCCTGCCCCGTCCACGGCTGCACCAGCTGCCCCGCCGCCCGCCCGGA A C APC2 Ensembl:ENSG00000115266 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1467925..1468100 26863196 MeRIP-seq:(Medium) rs1198071443 Functional Loss SNV dbSNP153 33..33 33 - - - 80404 RMVar_ID_80404 Human_SNP_ID_655426423 m1A Human chr19 - 1468435 1468435 1468435 GGATACGAAGGACAGGATGGAGTCGGACTCGGACGAGGCCTCCCGCGTGGCAGCTGCTGCCTGGT GGATACGAAGGACAGGATGGAGTCGGACTCGGGCGAGGCCTCCCGCGTGGCAGCTGCTGCCTGGT T C C19orf25 Ensembl:ENSG00000119559 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1468431..1468572 32194978 MeRIP-seq:(Medium) rs1365619947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18491458,Human_RBP_ID_22718643,Human_RBP_ID_24419206 RMVar_hsa_circ_115862,RMVar_hsa_circ_191083 80405 RMVar_ID_80405 Human_SNP_ID_655428429 m1A Human chr19 - 1473405 1473405 1473405 ACTCCTGGCCTCAGCCAGTGCCTCCCCGGCCCATCTGGGTGGGGTGCCCACAAACCCTGTGCCCC ACTCCTGGCCTCAGCCAGTGCCTCCCCGGCCCTTCTGGGTGGGGTGCCCACAAACCCTGTGCCCC T A C19orf25 Ensembl:ENSG00000119559 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1473361..1473759 32194978 MeRIP-seq:(Medium) rs1365167740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86633,RMVar_hsa_circ_115862,RMVar_hsa_circ_191083,RMVar_hsa_circ_122447,RMVar_hsa_circ_191085,RMVar_hsa_circ_191086 80406 RMVar_ID_80406 Human_SNP_ID_655428430 m1A Human chr19 - 1473405 1473405 1473405 ACTCCTGGCCTCAGCCAGTGCCTCCCCGGCCCATCTGGGTGGGGTGCCCACAAACCCTGTGCCCC ACTCCTGGCCTCAGCCAGTGCCTCCCCGGCCCGTCTGGGTGGGGTGCCCACAAACCCTGTGCCCC T C C19orf25 Ensembl:ENSG00000119559 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1473361..1473759 32194978 MeRIP-seq:(Medium) rs1365167740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86633,RMVar_hsa_circ_115862,RMVar_hsa_circ_191083,RMVar_hsa_circ_122447,RMVar_hsa_circ_191085,RMVar_hsa_circ_191086 80407 RMVar_ID_80407 Human_SNP_ID_655428636 m1A Human chr19 + 1473986 1473986 1473986 CAGGGAATAAGAAACATCTTCCACATTCAAGAAACAAAGCTGGCTGTGGGTCTGGAGAGAGGGTG CAGGGAATAAGAAACATCTTCCACATTCAAGAGACAAAGCTGGCTGTGGGTCTGGAGAGAGGGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1473907..1474007 32194978 MeRIP-seq:(Medium) rs1245256605 Functional Loss SNV dbSNP153 33..33 33 - - - 80408 RMVar_ID_80408 Human_SNP_ID_655429125 m1A Human chr19 + 1475128 1475128 1475128 TCCAGGTCCTCGCCGGCTCGCTGCAGGAGCTCACACCTCTGCCTCAGCACGTTGCCCGCCTGCTG TCCAGGTCCTCGCCGGCTCGCTGCAGGAGCTCCCACCTCTGCCTCAGCACGTTGCCCGCCTGCTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1474751..1475297 32194978 MeRIP-seq:(Medium) rs919576315 Functional Loss SNV dbSNP153 33..33 33 - - - 80409 RMVar_ID_80409 Human_SNP_ID_655429126 m1A Human chr19 + 1475128 1475128 1475128 TCCAGGTCCTCGCCGGCTCGCTGCAGGAGCTCACACCTCTGCCTCAGCACGTTGCCCGCCTGCTG TCCAGGTCCTCGCCGGCTCGCTGCAGGAGCTCGCACCTCTGCCTCAGCACGTTGCCCGCCTGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1474751..1475297 32194978 MeRIP-seq:(Medium) rs919576315 Functional Loss SNV dbSNP153 33..33 33 - - - 80410 RMVar_ID_80410 Human_SNP_ID_655429609 m1A Human chr19 + 1476430 1476430 1476430 CAGTTTCGCCACACTCAACGGCCATGGACCTGAGCCCATGAAGCTCAAACCACGGCCCCAGCACC CAGTTTCGCCACACTCAACGGCCATGGACCTGGGCCCATGAAGCTCAAACCACGGCCCCAGCACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1476429..1476711 26863196 MeRIP-seq:(Medium) rs1443025734 Functional Loss SNV dbSNP153 33..33 33 - - - 80411 RMVar_ID_80411 Human_SNP_ID_655430379 m1A Human chr19 - 1478696 1478696 1478696 CAGCAAGGGGACGGGAGAGAAGCACACCCCTAACTCCTGACCCCACGCCCTGGGAACCCCCGCAA CAGCAAGGGGACGGGAGAGAAGCACACCCCTAGCTCCTGACCCCACGCCCTGGGAACCCCCGCAA T C C19orf25 Ensembl:ENSG00000119559 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1478690..1479186 26863196 MeRIP-seq:(Medium) rs573794585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514489,Human_RBP_ID_8255826,Human_RBP_ID_9427885 Human_Splice_Rec_1932837 RMVar_hsa_circ_115862,RMVar_hsa_circ_191083,RMVar_hsa_circ_122447,RMVar_hsa_circ_191086 80412 RMVar_ID_80412 Human_SNP_ID_655433824 m1A Human chr19 - 1486951 1486951 1486951 ACACCAACAGCATCCACACGCTTTCCGTGGGCAGCACCACCCAGCAGGGCCGCGTGCCCTGGTAC ACACCAACAGCATCCACACGCTTTCCGTGGGCGGCACCACCCAGCAGGGCCGCGTGCCCTGGTAC T C PCSK4 Ensembl:ENSG00000115257 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1486947..1487032 26863196 MeRIP-seq:(Medium) rs753372220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1932876,Human_Splice_Rec_1932877,Human_Splice_Rec_1932901,Human_Splice_Rec_1932927,Human_Splice_Rec_1932949,Human_Splice_Rec_1932971 RMVar_hsa_circ_5997,RMVar_hsa_circ_49925 80413 RMVar_ID_80413 Human_SNP_ID_655435757 m1A Human chr19 + 1491245 1491245 1491245 GTGGGTGCCCTGGTCCGCGGGCGAGCTCGAGCAGCCAACCCCGGGCGCGTCGGGGCCATGGACGG GTGGGTGCCCTGGTCCGCGGGCGAGCTCGAGCGGCCAACCCCGGGCGCGTCGGGGCCATGGACGG A G REEP6 Ensembl:ENSG00000115255 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1491196..1491297 32194978 MeRIP-seq:(Medium) rs369454346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4556996,Human_RBP_ID_5319815,Human_RBP_ID_9328098,Human_RBP_ID_9425063,Human_RBP_ID_22447125,Human_RBP_ID_24375138,Human_RBP_ID_26471573 80414 RMVar_ID_80414 Human_SNP_ID_655435781 m1A Human chr19 + 1491295 1491295 1491295 CGGGGCCATGGACGGCCTGAGGCAGCGCGTGGAGCACTTCCTGGAGCAAAGGAACCTGGTCACCG CGGGGCCATGGACGGCCTGAGGCAGCGCGTGGGGCACTTCCTGGAGCAAAGGAACCTGGTCACCG A G REEP6 Ensembl:ENSG00000115255 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1491210..1491301 26863410 MeRIP-seq:(Medium) rs756957819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4506112,Human_RBP_ID_5144839,Human_RBP_ID_5319815 Human_Splice_Rec_1933031,Human_Splice_Rec_1933035,Human_Splice_Rec_1933043 80415 RMVar_ID_80415 Human_SNP_ID_655437977 m1A Human chr19 + 1497283 1497283 1497283 AGGAGGGGGCCGCGCCAGGCTCCCAGGCCTCCACAGAGTCTTCAGCGCATCCCCCAACAGCAGCC AGGAGGGGGCCGCGCCAGGCTCCCAGGCCTCCGCAGAGTCTTCAGCGCATCCCCCAACAGCAGCC A G REEP6 Ensembl:ENSG00000115255 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1497278..1497442 26863196 MeRIP-seq:(Medium) rs991002286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4506121 Human_Splice_Rec_1933059 RMVar_hsa_circ_77667,RMVar_hsa_circ_191088 80416 RMVar_ID_80416 Human_SNP_ID_655438075 m1A Human chr19 + 1497516 1497516 1497516 CGGGCACAGGGCAGCTCCCACTGGTCTCGGCAACACACCCAGCCGCCTGGTACTTCCTCCAGCCC CGGGCACAGGGCAGCTCCCACTGGTCTCGGCAGCACACCCAGCCGCCTGGTACTTCCTCCAGCCC A G REEP6 Ensembl:ENSG00000115255 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1497510..1497632 26863196 MeRIP-seq:(Medium) rs1437487830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082743,Human_RBP_ID_17386526,Human_RBP_ID_18946161,Human_RBP_ID_26471577 Human_miRNA_ID_1358311,Human_miRNA_ID_2943858 RMVar_hsa_circ_77667,RMVar_hsa_circ_191088 80417 RMVar_ID_80417 Human_SNP_ID_655441280 m1A Human chr19 - 1506823 1506823 1506823 AGGCTCGTGTGCAGGCCCTGGGCTGGCCCCTGAGGCAGCCTCAGCCCCGGGGGGTGGAGCCTCAG AGGCTCGTGTGCAGGCCCTGGGCTGGCCCCTGGGGCAGCCTCAGCCCCGGGGGGTGGAGCCTCAG T C ADAMTSL5 Ensembl:ENSG00000185761 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1506779..1508839 32194978 MeRIP-seq:(Medium) rs1397877349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1933079,Human_Splice_Rec_1933103,Human_Splice_Rec_1933123,Human_Splice_Rec_1933145 80418 RMVar_ID_80418 Human_SNP_ID_655441281 m1A Human chr19 - 1506823 1506823 1506823 AGGCTCGTGTGCAGGCCCTGGGCTGGCCCCTGAGGCAGCCTCAGCCCCGGGGGGTGGAGCCTCAG AGGCTCGTGTGCAGGCCCTGGGCTGGCCCCTGCGGCAGCCTCAGCCCCGGGGGGTGGAGCCTCAG T G ADAMTSL5 Ensembl:ENSG00000185761 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1506779..1508839 32194978 MeRIP-seq:(Medium) rs1397877349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1933079,Human_Splice_Rec_1933103,Human_Splice_Rec_1933123,Human_Splice_Rec_1933145 80419 RMVar_ID_80419 Human_SNP_ID_655441859 m1A Human chr19 + 1508024 1508024 1508024 AGTCACCGGCGTCACGAAACACGCGCTGCACGAAAAGGCACGAGTCGTTGGCGCCTCCGCAGCGG AGTCACCGGCGTCACGAAACACGCGCTGCACGGAAAGGCACGAGTCGTTGGCGCCTCCGCAGCGG A G PLK5 Ensembl:ENSG00000185988 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:1507981..1508133 26863196 MeRIP-seq:(Medium) rs1169130173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1933199 80420 RMVar_ID_80420 Human_SNP_ID_655459425 m1A Human chr19 - 1555220 1555216 1555220 CCTCCAGGGTGATCTTTAAAAAAGCAAAACAAAAAACACGACTTTTCCAGCGCTCAGCGTTTTTT CCTCCAGGGTGATCTTTAAAAAAGCAAAACAA____CACGACTTTTCCAGCGCTCAGCGTTTTTT GTTTT G MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1555118..1555219 32194978 MeRIP-seq:(Medium) rs971365560 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13383306,Human_RBP_ID_18301777 RMVar_hsa_circ_108671,RMVar_hsa_circ_191092 80421 RMVar_ID_80421 Human_SNP_ID_655459426 m1A Human chr19 - 1555220 1555216 1555220 CCTCCAGGGTGATCTTTAAAAAAGCAAAACAAAAAACACGACTTTTCCAGCGCTCAGCGTTTTTT CCTCCAGGGTGATCTTTAAAAAAGCAAAACAA_AAACACGACTTTTCCAGCGCTCAGCGTTTTTT GTTTT GTTT MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1555118..1555219 32194978 MeRIP-seq:(Medium) rs971365560 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13383306,Human_RBP_ID_18301777 RMVar_hsa_circ_108671,RMVar_hsa_circ_191092 80422 RMVar_ID_80422 Human_SNP_ID_655459527 m1A Human chr19 - 1555381 1555381 1555381 GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGACGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGTCGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC T A MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1555068..1555408 26863196 MeRIP-seq:(Medium) rs756753498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144840,Human_RBP_ID_6724215,Human_RBP_ID_8197190,Human_RBP_ID_8830121,Human_RBP_ID_9425646,Human_RBP_ID_17916220,Human_RBP_ID_18191609,Human_RBP_ID_24483738 Human_miRNA_ID_1541041 RMVar_hsa_circ_108671,RMVar_hsa_circ_191093,RMVar_hsa_circ_191092 80423 RMVar_ID_80423 Human_SNP_ID_655459528 m1A Human chr19 - 1555381 1555381 1555381 GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGACGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGGCGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC T C MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1555068..1555408 26863196 MeRIP-seq:(Medium) rs756753498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144840,Human_RBP_ID_6724215,Human_RBP_ID_8197190,Human_RBP_ID_8830121,Human_RBP_ID_9425646,Human_RBP_ID_17916220,Human_RBP_ID_18191609,Human_RBP_ID_24483738 Human_miRNA_ID_1541041 RMVar_hsa_circ_108671,RMVar_hsa_circ_191093,RMVar_hsa_circ_191092 80424 RMVar_ID_80424 Human_SNP_ID_655459529 m1A Human chr19 - 1555381 1555381 1555381 GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGACGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGCCGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC T G MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1555068..1555408 26863196 MeRIP-seq:(Medium) rs756753498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144840,Human_RBP_ID_6724215,Human_RBP_ID_8197190,Human_RBP_ID_8830121,Human_RBP_ID_9425646,Human_RBP_ID_17916220,Human_RBP_ID_18191609,Human_RBP_ID_24483738 Human_miRNA_ID_1541041 RMVar_hsa_circ_108671,RMVar_hsa_circ_191093,RMVar_hsa_circ_191092 80425 RMVar_ID_80425 Human_SNP_ID_655459685 m1A Human chr19 - 1555535 1555535 1555535 CCTAGAGCGCGGACCACCACGTGGCCGGGGCCATCTGCGGGGGCCAGGGGTGGGCGCGGGAGACG CCTAGAGCGCGGACCACCACGTGGCCGGGGCCTTCTGCGGGGGCCAGGGGTGGGCGCGGGAGACG T A MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1555488..1556218 26863196 MeRIP-seq:(Medium) rs1054734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6724218,Human_RBP_ID_17916223,Human_RBP_ID_27562058 RMVar_hsa_circ_191093 80426 RMVar_ID_80426 Human_SNP_ID_655459777 m1A Human chr19 + 1555693 1555693 1555693 AGAGGTTGTGGCCGCAGGGGACCAGCGCAGCCATCACCTCGCCCTCGGCGCACACCACGCACTCT AGAGGTTGTGGCCGCAGGGGACCAGCGCAGCCGTCACCTCGCCCTCGGCGCACACCACGCACTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1555518..1556200 26863196 MeRIP-seq:(Medium) rs747339955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191094 80427 RMVar_ID_80427 Human_SNP_ID_655459915 m1A Human chr19 - 1555879 1555879 1555879 CCCGGTGGGCGCGCTGTCCTGGCGACCCCCGCAGGGCCCCGTATCCTTCCCAGGCGGCGCCGCCT CCCGGTGGGCGCGCTGTCCTGGCGACCCCCGCGGGGCCCCGTATCCTTCCCAGGCGGCGCCGCCT T C MEX3D Ensembl:ENSG00000181588 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1555868..1556069 26863196 MeRIP-seq:(Medium) rs1302229388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4506917,Human_RBP_ID_27464460 RMVar_hsa_circ_191093 80428 RMVar_ID_80428 Human_SNP_ID_655460085 m1A Human chr19 - 1556186 1556186 1556186 TCGGCGCGGAGGGTCCCGGTGCCCCGGTGGGGACGGCCGCCCCCGACGACTGCGACTTCGGCTTC TCGGCGCGGAGGGTCCCGGTGCCCCGGTGGGGTCGGCCGCCCCCGACGACTGCGACTTCGGCTTC T A MEX3D Ensembl:ENSG00000181588 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1555528..1556368 26863196 MeRIP-seq:(Medium) rs767696571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27464464 RMVar_hsa_circ_191093 80429 RMVar_ID_80429 Human_SNP_ID_655460279 m1A Human chr19 + 1556500 1556500 1556500 CGGGGCCCGCGTCGGTGAAGGCGCCAGTGCGCAGCGTGATGTGCGCCTCGATCTCCTCGCGCGCG CGGGGCCCGCGTCGGTGAAGGCGCCAGTGCGCCGCGTGATGTGCGCCTCGATCTCCTCGCGCGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1556449..1556545 26863196 MeRIP-seq:(Medium) rs779893241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191094 80430 RMVar_ID_80430 Human_SNP_ID_655460280 m1A Human chr19 + 1556500 1556500 1556500 CGGGGCCCGCGTCGGTGAAGGCGCCAGTGCGCAGCGTGATGTGCGCCTCGATCTCCTCGCGCGCG CGGGGCCCGCGTCGGTGAAGGCGCCAGTGCGCTGCGTGATGTGCGCCTCGATCTCCTCGCGCGCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1556449..1556545 26863196 MeRIP-seq:(Medium) rs779893241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191094 80431 RMVar_ID_80431 Human_SNP_ID_655460309 m1A Human chr19 - 1556581 1556581 1556581 GACGCACACCTACATCGTGACGCCCGGGCGCGACAAGGAGCCGGTGTTCGCGGTCACTGGGATGC GACGCACACCTACATCGTGACGCCCGGGCGCGGCAAGGAGCCGGTGTTCGCGGTCACTGGGATGC T C MEX3D Ensembl:ENSG00000181588 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1555568..1567608 32194978 MeRIP-seq:(Medium) rs865932980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309317,Human_RBP_ID_27464472 RMVar_hsa_circ_191093 80432 RMVar_ID_80432 Human_SNP_ID_655463905 m1A Human chr19 + 1567765 1567765 1567765 GCCTCAGGTCCGTCGGGGGGCACAGGCTCCGGAGCCGCCCCGCCGTCCGCGCCCCCCGCCGCCGC GCCTCAGGTCCGTCGGGGGGCACAGGCTCCGGGGCCGCCCCGCCGTCCGCGCCCCCCGCCGCCGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:1567590..1568288 26863410 MeRIP-seq:(Medium) rs1239083427 Functional Loss SNV dbSNP153 33..33 33 - - - 80433 RMVar_ID_80433 Human_SNP_ID_655463922 m1A Human chr19 - 1567805 1567805 1567805 TGGCGACACGGACGAGGAGGGGGCGGCCGGGGACGGCGCAGCGGCGGCGGGGGGCGCGGACGGCG TGGCGACACGGACGAGGAGGGGGCGGCCGGGGGCGGCGCAGCGGCGGCGGGGGGCGCGGACGGCG T C MEX3D Ensembl:ENSG00000181588 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1567730..1567822 26863410 MeRIP-seq:(Medium) rs923611086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557003,Human_RBP_ID_9293127,Human_RBP_ID_9328107 80434 RMVar_ID_80434 Human_SNP_ID_655467131 m1A Human chr19 - 1577001 1577001 1577001 GGACTGATGGGCAGAGTCGCCCCTGTGGCTGGACTGTGACCATCCCTGATGGGGCCTGACCGCGG GGACTGATGGGCAGAGTCGCCCCTGTGGCTGGGCTGTGACCATCCCTGATGGGGCCTGACCGCGG T C MBD3 Ensembl:ENSG00000071655 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1576901..1577194 26863410 MeRIP-seq:(Medium) rs1280686508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514866,Human_RBP_ID_5239517,Human_RBP_ID_6724302,Human_RBP_ID_8478774,Human_RBP_ID_8830140,Human_RBP_ID_13383425,Human_RBP_ID_18165901,Human_RBP_ID_26471584,Human_RBP_ID_27269222,Human_RBP_ID_27464514 Human_miRNA_ID_161534,Human_miRNA_ID_708424,Human_miRNA_ID_715683,Human_miRNA_ID_1329243,Human_miRNA_ID_1957650,Human_miRNA_ID_2286609,Human_miRNA_ID_2289608,Human_miRNA_ID_2657690,Human_miRNA_ID_2974907,Human_miRNA_ID_3008104 RMVar_hsa_circ_118764,RMVar_hsa_circ_124358,RMVar_hsa_circ_191098,RMVar_hsa_circ_86392,RMVar_hsa_circ_88017,RMVar_hsa_circ_82453,RMVar_hsa_circ_191099,RMVar_hsa_circ_191096,RMVar_hsa_circ_191097,RMVar_hsa_circ_191095 80435 RMVar_ID_80435 Human_SNP_ID_655467706 m1A Human chr19 - 1578461 1578461 1578461 GGCGCTGATGGCCGACATGCTGGCGCACGTGGAGGAGCTGGCCCGTGACGGGGAGGCGCCGCTGG GGCGCTGATGGCCGACATGCTGGCGCACGTGGGGGAGCTGGCCCGTGACGGGGAGGCGCCGCTGG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1578451..1578550 26863196 MeRIP-seq:(Medium) rs749633456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5117641,Human_RBP_ID_6724345,Human_RBP_ID_9379970,Human_RBP_ID_17916287,Human_RBP_ID_18440681,Human_RBP_ID_18995787,Human_RBP_ID_26336932,Human_RBP_ID_26473087 Human_Splice_Rec_1933390,Human_Splice_Rec_1933402,Human_Splice_Rec_1933412,Human_Splice_Rec_1933422,Human_Splice_Rec_1933430,Human_Splice_Rec_1933436,Human_Splice_Rec_1933440,Human_Splice_Rec_1933476 RMVar_hsa_circ_46920,RMVar_hsa_circ_118764,RMVar_hsa_circ_124358,RMVar_hsa_circ_191098,RMVar_hsa_circ_86392,RMVar_hsa_circ_88017,RMVar_hsa_circ_82453,RMVar_hsa_circ_191099,RMVar_hsa_circ_191096,RMVar_hsa_circ_191097,RMVar_hsa_circ_191095 80436 RMVar_ID_80436 Human_SNP_ID_655467724 m1A Human chr19 - 1578486 1578483 1578486 AGCAGGTGCGGAAGCGGCTGGAGGAGGCGCTGATGGCCGACATGCTGGCGCACGTGGAGGAGCTG AGCAGGTGCGGAAGCGGCTGGAGGAGGCGCTG___GCCGACATGCTGGCGCACGTGGAGGAGCTG CCAT C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1577369..1581275 26863196 MeRIP-seq:(Medium) rs1290583458 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_914140,Human_RBP_ID_1013457,Human_RBP_ID_6724345,Human_RBP_ID_9381549,Human_RBP_ID_17916287,Human_RBP_ID_26336932 Human_Splice_Rec_1933390,Human_Splice_Rec_1933402,Human_Splice_Rec_1933412,Human_Splice_Rec_1933422,Human_Splice_Rec_1933430,Human_Splice_Rec_1933436,Human_Splice_Rec_1933440,Human_Splice_Rec_1933476 RMVar_hsa_circ_46920,RMVar_hsa_circ_118764,RMVar_hsa_circ_124358,RMVar_hsa_circ_191098,RMVar_hsa_circ_86392,RMVar_hsa_circ_88017,RMVar_hsa_circ_82453,RMVar_hsa_circ_191099,RMVar_hsa_circ_191096,RMVar_hsa_circ_191097,RMVar_hsa_circ_191095 80437 RMVar_ID_80437 Human_SNP_ID_655467745 m1A Human chr19 - 1578529 1578529 1578529 ACGCAAGGTCCATGTGTCCCCAGGAAGCAGGAAGAGCTGGTGCAGCAGGTGCGGAAGCGGCTGGA ACGCAAGGTCCATGTGTCCCCAGGAAGCAGGAGGAGCTGGTGCAGCAGGTGCGGAAGCGGCTGGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1578326..1578550 26863196 MeRIP-seq:(Medium) rs779394990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4507146,Human_RBP_ID_5374830,Human_RBP_ID_6724345,Human_RBP_ID_17916288,Human_RBP_ID_22663388,Human_RBP_ID_26336932 Human_Splice_Rec_1933390,Human_Splice_Rec_1933402,Human_Splice_Rec_1933412,Human_Splice_Rec_1933422,Human_Splice_Rec_1933430,Human_Splice_Rec_1933436,Human_Splice_Rec_1933440,Human_Splice_Rec_1933476 RMVar_hsa_circ_46920,RMVar_hsa_circ_118764,RMVar_hsa_circ_124358,RMVar_hsa_circ_191098,RMVar_hsa_circ_86392,RMVar_hsa_circ_88017,RMVar_hsa_circ_82453,RMVar_hsa_circ_191099,RMVar_hsa_circ_191096,RMVar_hsa_circ_191097,RMVar_hsa_circ_191095 80438 RMVar_ID_80438 Human_SNP_ID_655469240 m1A Human chr19 + 1582578 1582578 1582578 GGAGATGAGGGCACCTGCAGCACCTCCACCCCACCCGGCACATCCCCTTCCGCCTCCCCTCAGGG GGAGATGAGGGCACCTGCAGCACCTCCACCCCCCCCGGCACATCCCCTTCCGCCTCCCCTCAGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:1582576..1582655;chr19:1582572..1582710 26863196 MeRIP-seq:(Medium) rs749328438 Functional Loss SNV dbSNP153 33..33 33 - - - 80439 RMVar_ID_80439 Human_SNP_ID_655469241 m1A Human chr19 + 1582578 1582578 1582578 GGAGATGAGGGCACCTGCAGCACCTCCACCCCACCCGGCACATCCCCTTCCGCCTCCCCTCAGGG GGAGATGAGGGCACCTGCAGCACCTCCACCCCGCCCGGCACATCCCCTTCCGCCTCCCCTCAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:1582576..1582655;chr19:1582572..1582710 26863196 MeRIP-seq:(Medium) rs749328438 Functional Loss SNV dbSNP153 33..33 33 - - - 80440 RMVar_ID_80440 Human_SNP_ID_655470261 m1A Human chr19 + 1585179 1585179 1585179 TCAGGTCCATGGAGCCGCCCAGGTAGCGCGCCAGCTGCGGCTTGCTGCGGAACTTCTTCCCGCTC TCAGGTCCATGGAGCCGCCCAGGTAGCGCGCCCGCTGCGGCTTGCTGCGGAACTTCTTCCCGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1584826..1585290;chr19:1584826..1585582;chr19:1583368..1585277 26863196 MeRIP-seq:(Medium) rs868396759 Functional Loss SNV dbSNP153 33..33 33 - - - 80441 RMVar_ID_80441 Human_SNP_ID_655470352 m1A Human chr19 + 1585377 1585377 1585377 CCTGACCCCAAACCCAGGCAGGCCCTGGCCCCAGCCCCAGACCCCAACCCTGGCGTGACCCCAGA CCTGACCCCAAACCCAGGCAGGCCCTGGCCCCCGCCCCAGACCCCAACCCTGGCGTGACCCCAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1585375..1585980 26863196 MeRIP-seq:(Medium) rs1441999419 Functional Loss SNV dbSNP153 33..33 33 - - - 80442 RMVar_ID_80442 Human_SNP_ID_655471086 m1A Human chr19 - 1587685 1587685 1587685 AAGACACCAGCCAGGCATAGTGGCTGCCGCCTATAATCCCTTTGGGAGGTCGAGGCAGGAGGATC AAGACACCAGCCAGGCATAGTGGCTGCCGCCTGTAATCCCTTTGGGAGGTCGAGGCAGGAGGATC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs939387928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4507231,Human_RBP_ID_6724425,Human_RBP_ID_13383639,Human_RBP_ID_17916328,Human_RBP_ID_25387233,Human_RBP_ID_26471595 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 80443 RMVar_ID_80443 Human_SNP_ID_655471981 m1A Human chr19 - 1590506 1590503 1590506 TCAGGCGACCCTCTCAGCTCAGCCTCCCAAGTAGTGGGAATTACAGGCACGTGCCACCATACCTG TCAGGCGACCCTCTCAGCTCAGCCTCCCAAGT___GGGAATTACAGGCACGTGCCACCATACCTG CACT C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs535008726 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 80444 RMVar_ID_80444 Human_SNP_ID_655472906 m1A Human chr19 + 1592685 1592685 1592685 CCGCCGGGCCCGCCGCCGCCGCCCGGACCCCCACTCGCCGCCGCCGCCTCAGCTGCCTCCGCTGC CCGCCGGGCCCGCCGCCGCCGCCCGGACCCCCCCTCGCCGCCGCCGCCTCAGCTGCCTCCGCTGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:1592562..1592825 26863196 MeRIP-seq:(Medium) rs991925636 Functional Loss SNV dbSNP153 33..33 33 - - - 80445 RMVar_ID_80445 Human_SNP_ID_655472910 m1A Human chr19 - 1592710 1592689 1592710 GCGGCAAGTGGCGGCGGCGGCAGCGGCAGCGGAGGCAGCTGAGGCGGCGGCGGCGAGTGGGGGTC GCGGCAAGTGGCGGCGGCGGCAGCGGCAGCGG_____________________CGAGTGGGGGTC GCCGCCGCCGCCTCAGCTGCCT G MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr19:1592558..1592825;chr19:1585210..1605397 26863196,26863410 MeRIP-seq:(Medium) rs916523388 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_5320900,Human_RBP_ID_8942116,Human_RBP_ID_9328113,Human_RBP_ID_13383927,Human_RBP_ID_26471600 Human_Splice_Rec_1933381 80446 RMVar_ID_80446 Human_SNP_ID_655472926 m1A Human chr19 - 1592715 1592710 1592716 CAGCCGCGGCAAGTGGCGGCGGCGGCAGCGGCAGCGGAGGCAGCTGAGGCGGCGGCGGCGAGTGG CAGCCGCGGCAAGTGGCGGCGGCGGCAGCGG______AGGCAGCTGAGGCGGCGGCGGCGAGTGG TCCGCTG T MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:1592601..1592800 26863410 MeRIP-seq:(Medium) rs1012473361 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_4557010,Human_RBP_ID_5320900,Human_RBP_ID_8942116,Human_RBP_ID_9328113,Human_RBP_ID_9425653,Human_RBP_ID_13383927,Human_RBP_ID_26471600 Human_Splice_Rec_1933381 80447 RMVar_ID_80447 Human_SNP_ID_655472935 m1A Human chr19 - 1592721 1592721 1592721 CCGGAACAGCCGCGGCAAGTGGCGGCGGCGGCAGCGGCAGCGGAGGCAGCTGAGGCGGCGGCGGC CCGGAACAGCCGCGGCAAGTGGCGGCGGCGGCGGCGGCAGCGGAGGCAGCTGAGGCGGCGGCGGC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1592626..1592800 26863410 MeRIP-seq:(Medium) rs1015297786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4507385,Human_RBP_ID_5117643,Human_RBP_ID_5320900,Human_RBP_ID_8942116,Human_RBP_ID_9328113,Human_RBP_ID_9425653,Human_RBP_ID_18420822,Human_RBP_ID_26471600 80448 RMVar_ID_80448 Human_SNP_ID_655474524 m1A Human chr19 + 1597493 1597493 1597493 GATAAACAGGCTGTGGCGGAAGTGATCACGTGAGACTTCTCAGGGTGGCTCATAGAAGCACTGTG GATAAACAGGCTGTGGCGGAAGTGATCACGTGGGACTTCTCAGGGTGGCTCATAGAAGCACTGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1597220..1597661 32194978 MeRIP-seq:(Medium) rs1205964082 Functional Loss SNV dbSNP153 33..33 33 - - - 80449 RMVar_ID_80449 Human_SNP_ID_655475098 m1A Human chr19 - 1599445 1599445 1599445 TACCTTACATCAATGGCAAGTTTAAGAAGGATAATTAATTACACAAACCCTTCACAGACTGCTCT TACCTTACATCAATGGCAAGTTTAAGAAGGATGATTAATTACACAAACCCTTCACAGACTGCTCT T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1576743..1605450 32194978 MeRIP-seq:(Medium) rs769058318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013492,Human_RBP_ID_1555985,Human_RBP_ID_1880826,Human_RBP_ID_4507433,Human_RBP_ID_5115943,Human_RBP_ID_5319820,Human_RBP_ID_5421222,Human_RBP_ID_5499014,Human_RBP_ID_5585430,Human_RBP_ID_6724618,Human_RBP_ID_8095909,Human_RBP_ID_8478839,Human_RBP_ID_9084832,Human_RBP_ID_13384017,Human_RBP_ID_17266960,Human_RBP_ID_17382301,Human_RBP_ID_17498086,Human_RBP_ID_17655755,Human_RBP_ID_17694758,Human_RBP_ID_17916397,Human_RBP_ID_18723844,Human_RBP_ID_22449121,Human_RBP_ID_23279499,Human_RBP_ID_23784737,Human_RBP_ID_24374756,Human_RBP_ID_24483740,Human_RBP_ID_26816517,Human_RBP_ID_27269309,Human_RBP_ID_27473293,Human_RBP_ID_27675032 Human_Splice_Rec_1933467,Human_Splice_Rec_1933479,Human_Splice_Rec_1933483,Human_Splice_Rec_1933487,Human_Splice_Rec_1933493 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 80450 RMVar_ID_80450 Human_SNP_ID_655475112 m1A Human chr19 + 1599486 1599486 1599486 TAAACTTGCCATTGATGTAAGGTACCCAGTCCAGGATCAGCCGCCAATCGGTGGCCCACACCAGC TAAACTTGCCATTGATGTAAGGTACCCAGTCCGGGATCAGCCGCCAATCGGTGGCCCACACCAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1599476..1599550 26863196 MeRIP-seq:(Medium) rs986001762 Functional Loss SNV dbSNP153 33..33 33 - - - 80451 RMVar_ID_80451 Human_SNP_ID_655475119 m1A Human chr19 + 1599499 1599499 1599499 GATGTAAGGTACCCAGTCCAGGATCAGCCGCCAATCGGTGGCCCACACCAGCCCCACGGCGCCCA GATGTAAGGTACCCAGTCCAGGATCAGCCGCCGATCGGTGGCCCACACCAGCCCCACGGCGCCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:1599369..1605475;chr19:1599451..1599525;chr19:1599426..1599525 26863196 MeRIP-seq:(Medium) rs1568282156 Functional Loss SNV dbSNP153 33..33 33 - - - 80452 RMVar_ID_80452 Human_SNP_ID_655475121 m1A Human chr19 - 1599501 1599501 1599501 TGTGGGCGCCGTGGGGCTGGTGTGGGCCACCGATTGGCGGCTGATCCTGGACTGGGTACCTTACA TGTGGGCGCCGTGGGGCTGGTGTGGGCCACCGTTTGGCGGCTGATCCTGGACTGGGTACCTTACA T A UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1599451..1599596 26863196 MeRIP-seq:(Medium) rs757125551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514964,Human_RBP_ID_771384,Human_RBP_ID_1013494,Human_RBP_ID_1555989,Human_RBP_ID_4507433,Human_RBP_ID_5115944,Human_RBP_ID_5319820,Human_RBP_ID_8830208,Human_RBP_ID_8942117,Human_RBP_ID_9084833,Human_RBP_ID_9328114,Human_RBP_ID_13384017,Human_RBP_ID_17655285,Human_RBP_ID_17916399,Human_RBP_ID_22446292,Human_RBP_ID_23784738,Human_RBP_ID_26984479,Human_RBP_ID_27573058 Human_Splice_Rec_1933466,Human_Splice_Rec_1933467,Human_Splice_Rec_1933478,Human_Splice_Rec_1933479,Human_Splice_Rec_1933482,Human_Splice_Rec_1933483,Human_Splice_Rec_1933486,Human_Splice_Rec_1933487,Human_Splice_Rec_1933492,Human_Splice_Rec_1933493,Human_Splice_Rec_1933496 Human_miRNA_ID_3010956 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 80453 RMVar_ID_80453 Human_SNP_ID_655475152 m1A Human chr19 + 1599541 1599541 1599541 CCACACCAGCCCCACGGCGCCCACAGCGCCCCATGTGTAGGCCGTCGGGACCCTGCGAGAGGAGA CCACACCAGCCCCACGGCGCCCACAGCGCCCCGTGTGTAGGCCGTCGGGACCCTGCGAGAGGAGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1599526..1599550 26863196 MeRIP-seq:(Medium) rs1285715834 Functional Loss SNV dbSNP153 33..33 33 - - - 80454 RMVar_ID_80454 Human_SNP_ID_655476277 m1A Human chr19 + 1603113 1603113 1603113 TCCTGGGGATGAGACCCGCTCCCTAGCCTCCCAAAGCCACTGCCTGGTGGCACAGCCCTGCACGG TCCTGGGGATGAGACCCGCTCCCTAGCCTCCCGAAGCCACTGCCTGGTGGCACAGCCCTGCACGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1603110..1603240 26863196 MeRIP-seq:(Medium) rs1258527602 Functional Loss SNV dbSNP153 33..33 33 - - - 80455 RMVar_ID_80455 Human_SNP_ID_655476957 m1A Human chr19 - 1605409 1605409 1605409 CAGGGTCATCCTGAGGGTGCGACTCCGCCGCGATGGTGACCCGGTTCCTGGGCCCACGCTACCGG CAGGGTCATCCTGAGGGTGCGACTCCGCCGCGGTGGTGACCCGGTTCCTGGGCCCACGCTACCGG T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding start codon,start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1602409..1605475;chr19:1605297..1605475 26863196 MeRIP-seq:(Medium) rs1487630794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240109,Human_RBP_ID_514972,Human_RBP_ID_771385,Human_RBP_ID_826240,Human_RBP_ID_1555993,Human_RBP_ID_4557014,Human_RBP_ID_5144847,Human_RBP_ID_5319822,Human_RBP_ID_8478845,Human_RBP_ID_9328115,Human_RBP_ID_17655287,Human_RBP_ID_18421519,Human_RBP_ID_22446293,Human_RBP_ID_22501826,Human_RBP_ID_23130784,Human_RBP_ID_23784745,Human_RBP_ID_26984481 Human_Splice_Rec_1933465,Human_Splice_Rec_1933477,Human_Splice_Rec_1933485,Human_Splice_Rec_1933489,Human_Splice_Rec_1933495 Human_miRNA_ID_3089116 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 80456 RMVar_ID_80456 Human_SNP_ID_655478694 m1A Human chr19 - 1609927 1609927 1609927 TTCATGCCCCTCCCTGCATTGAGGCCTTGTGGACCCCTGGGCTGGCTGTGTTCATCCCCGCTGCA TTCATGCCCCTCCCTGCATTGAGGCCTTGTGGGCCCCTGGGCTGGCTGTGTTCATCCCCGCTGCA T C TCF3 Ensembl:ENSG00000071564 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1609588..1610187 32194978 MeRIP-seq:(Medium) rs896916384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514991,Human_RBP_ID_8478850,Human_RBP_ID_8830209,Human_RBP_ID_17916406 RMVar_hsa_circ_267745 80457 RMVar_ID_80457 Human_SNP_ID_655481129 m1A Human chr19 - 1615679 1615679 1615679 CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAACCCACCCCTCGGCACTCCCCACCCTCACCCCA CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCATCCCACCCCTCGGCACTCCCCACCCTCACCCCA T A TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1615676..1615825 26863196 MeRIP-seq:(Medium) rs773006419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99682,RMVar_hsa_circ_267745,RMVar_hsa_circ_34083,RMVar_hsa_circ_117817,RMVar_hsa_circ_376315,RMVar_hsa_circ_110050,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_191104 80458 RMVar_ID_80458 Human_SNP_ID_655481130 m1A Human chr19 - 1615679 1615679 1615679 CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAACCCACCCCTCGGCACTCCCCACCCTCACCCCA CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAGCCCACCCCTCGGCACTCCCCACCCTCACCCCA T C TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1615676..1615825 26863196 MeRIP-seq:(Medium) rs773006419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99682,RMVar_hsa_circ_267745,RMVar_hsa_circ_34083,RMVar_hsa_circ_117817,RMVar_hsa_circ_376315,RMVar_hsa_circ_110050,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_191104 80459 RMVar_ID_80459 Human_SNP_ID_655481131 m1A Human chr19 - 1615679 1615679 1615679 CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAACCCACCCCTCGGCACTCCCCACCCTCACCCCA CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCACCCCACCCCTCGGCACTCCCCACCCTCACCCCA T G TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1615676..1615825 26863196 MeRIP-seq:(Medium) rs773006419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99682,RMVar_hsa_circ_267745,RMVar_hsa_circ_34083,RMVar_hsa_circ_117817,RMVar_hsa_circ_376315,RMVar_hsa_circ_110050,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_191104 80460 RMVar_ID_80460 Human_SNP_ID_655482426 m1A Human chr19 - 1619176 1619176 1619176 CCTCGCAGGCAGCACCAGCCTCATGCACAACCACGCGGCCCTCCCCAGCCAGCCAGGCACCCTCC CCTCGCAGGCAGCACCAGCCTCATGCACAACCGCGCGGCCCTCCCCAGCCAGCCAGGCACCCTCC T C TCF3 Ensembl:ENSG00000071564 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1618978..1619307 26863196 MeRIP-seq:(Medium) rs772237833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4563265,Human_RBP_ID_26814844 Human_Splice_Rec_1933524,Human_Splice_Rec_1933525,Human_Splice_Rec_1933558,Human_Splice_Rec_1933559,Human_Splice_Rec_1933602,Human_Splice_Rec_1933603,Human_Splice_Rec_1933638,Human_Splice_Rec_1933639,Human_Splice_Rec_1933647,Human_Splice_Rec_1933655,Human_Splice_Rec_1933690,Human_Splice_Rec_1933691,Human_Splice_Rec_1933710,Human_Splice_Rec_1933711,Human_Splice_Rec_1933719,Human_Splice_Rec_1933727,Human_Splice_Rec_1933762,Human_Splice_Rec_1933763,Human_Splice_Rec_1933767,Human_Splice_Rec_1933786,Human_Splice_Rec_1933787,Human_Splice_Rec_1933804,Human_Splice_Rec_1933805,Human_Splice_Rec_1933810,Human_Splice_Rec_1933811 Human_miRNA_ID_2368178,Human_miRNA_ID_2686032,Human_miRNA_ID_3015962 RMVar_hsa_circ_99682,RMVar_hsa_circ_267745,RMVar_hsa_circ_34083,RMVar_hsa_circ_117817,RMVar_hsa_circ_110050,RMVar_hsa_circ_52475,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_372887,RMVar_hsa_circ_37164,RMVar_hsa_circ_191108 80461 RMVar_ID_80461 Human_SNP_ID_655483422 m1A Human chr19 + 1621165 1621162 1621165 CGAGGCCAGTGCTTTGCCGAGGGCATCCCCGGAGCTGCCAGCTGTGGTCCCTCGGGAGCCTGTGG CGAGGCCAGTGCTTTGCCGAGGGCATCCCC___GCTGCCAGCTGTGGTCCCTCGGGAGCCTGTGG CGGA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1615676..1622225 32194978 MeRIP-seq:(Medium) rs1047408874 Functional Loss DEL dbSNP153 31..33 33 - - - 80462 RMVar_ID_80462 Human_SNP_ID_655483824 m1A Human chr19 - 1621923 1621923 1621923 GGAGCAGAGGTGAACGGTGGGCTCCCATCTGCATCCTCCTTCTCCTCAGCCCCCGGAGCCACGTA GGAGCAGAGGTGAACGGTGGGCTCCCATCTGCGTCCTCCTTCTCCTCAGCCCCCGGAGCCACGTA T C TCF3 Ensembl:ENSG00000071564 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1621811..1621922 26863196 MeRIP-seq:(Medium) rs1484552955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52717,Human_RBP_ID_3955812,Human_RBP_ID_5115946,Human_RBP_ID_5144851,Human_RBP_ID_6724717,Human_RBP_ID_8095912,Human_RBP_ID_18191638,Human_RBP_ID_22533256 Human_Splice_Rec_1933514,Human_Splice_Rec_1933515,Human_Splice_Rec_1933548,Human_Splice_Rec_1933549,Human_Splice_Rec_1933592,Human_Splice_Rec_1933593,Human_Splice_Rec_1933628,Human_Splice_Rec_1933629,Human_Splice_Rec_1933680,Human_Splice_Rec_1933681,Human_Splice_Rec_1933752,Human_Splice_Rec_1933753,Human_Splice_Rec_1933776,Human_Splice_Rec_1933777 Human_miRNA_ID_2370902,Human_miRNA_ID_2467476,Human_miRNA_ID_2707186 RMVar_hsa_circ_32582,RMVar_hsa_circ_99682,RMVar_hsa_circ_117817,RMVar_hsa_circ_110050,RMVar_hsa_circ_52475,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_37164,RMVar_hsa_circ_191109,RMVar_hsa_circ_29944,RMVar_hsa_circ_36109,RMVar_hsa_circ_118391 80463 RMVar_ID_80463 Human_SNP_ID_655484070 m1A Human chr19 + 1622337 1622337 1622337 CCATGTACCTGCCACGTAGAAGGGGGCGGGATAGGTGCTGCTGGGGGTCTTGGCGGACGGGTAGG CCATGTACCTGCCACGTAGAAGGGGGCGGGATTGGTGCTGCTGGGGGTCTTGGCGGACGGGTAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1622104..1625744 26863196 MeRIP-seq:(Medium) rs1234674635 Functional Loss SNV dbSNP153 33..33 33 - - - 80464 RMVar_ID_80464 Human_SNP_ID_655486171 m1A Human chr19 - 1627423 1627423 1627423 TCCCACTAACCTTCCTTCTCCCCTTGCAGGCAAGAGCGGTGAGCGGGGCGCCTATGCCTCCTTCG TCCCACTAACCTTCCTTCTCCCCTTGCAGGCAGGAGCGGTGAGCGGGGCGCCTATGCCTCCTTCG T C TCF3 Ensembl:ENSG00000071564 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1627401..1627425 26863196 MeRIP-seq:(Medium) rs41275842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913985,Human_RBP_ID_3954013,Human_RBP_ID_4507751,Human_RBP_ID_9293148,Human_RBP_ID_17271711,Human_RBP_ID_18165373,Human_RBP_ID_18993976,Human_RBP_ID_22661552,Human_RBP_ID_27269396 Human_Splice_Rec_1933504,Human_Splice_Rec_1933505,Human_Splice_Rec_1933538,Human_Splice_Rec_1933539,Human_Splice_Rec_1933582,Human_Splice_Rec_1933583,Human_Splice_Rec_1933618,Human_Splice_Rec_1933619,Human_Splice_Rec_1933671,Human_Splice_Rec_1933742,Human_Splice_Rec_1933743,Human_Splice_Rec_1933820,Human_Splice_Rec_1933821 RMVar_hsa_circ_32582,RMVar_hsa_circ_99682,RMVar_hsa_circ_110050,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_37164,RMVar_hsa_circ_114384,RMVar_hsa_circ_191109,RMVar_hsa_circ_118391,RMVar_hsa_circ_191110,RMVar_hsa_circ_124478,RMVar_hsa_circ_342881,RMVar_hsa_circ_191111,RMVar_hsa_circ_269851,RMVar_hsa_circ_312197,RMVar_hsa_circ_191112 80465 RMVar_ID_80465 Human_SNP_ID_655486304 m1A Human chr19 + 1627657 1627657 1627657 GCCCTGCCCTCAGTGTGCCCATCTCCTGCCCAATGACAGGCTTGGGGACAAGAAGGGGTCCCCGA GCCCTGCCCTCAGTGTGCCCATCTCCTGCCCAGTGACAGGCTTGGGGACAAGAAGGGGTCCCCGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1627655..1627782 26863196 MeRIP-seq:(Medium) rs146707702 Functional Loss SNV dbSNP153 33..33 33 - - - 80466 RMVar_ID_80466 Human_SNP_ID_655496169 m1A Human chr19 - 1651501 1651501 1651501 CTCGCCACCCCCCCAACTAAGTCTGTCTTAAAATCGGTTTCAGCTACCCCACAAAAAAGTGCGGT CTCGCCACCCCCCCAACTAAGTCTGTCTTAAATTCGGTTTCAGCTACCCCACAAAAAAGTGCGGT T A TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1651496..1651621 26863196 MeRIP-seq:(Medium) rs1392504916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8101564,Human_RBP_ID_8197207 RMVar_hsa_circ_99682,RMVar_hsa_circ_191107 80467 RMVar_ID_80467 Human_SNP_ID_655496170 m1A Human chr19 - 1651501 1651501 1651501 CTCGCCACCCCCCCAACTAAGTCTGTCTTAAAATCGGTTTCAGCTACCCCACAAAAAAGTGCGGT CTCGCCACCCCCCCAACTAAGTCTGTCTTAAAGTCGGTTTCAGCTACCCCACAAAAAAGTGCGGT T C TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1651496..1651621 26863196 MeRIP-seq:(Medium) rs1392504916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8101564,Human_RBP_ID_8197207 RMVar_hsa_circ_99682,RMVar_hsa_circ_191107 80468 RMVar_ID_80468 Human_SNP_ID_655496514 m1A Human chr19 - 1652038 1652038 1652038 CGTCGGGCCGGGCACTTCGGGAAACTTTAAGCAGCCCCGGGCGGGGGCGCGGGGGGCGCCGGACG CGTCGGGCCGGGCACTTCGGGAAACTTTAAGCCGCCCCGGGCGGGGGCGCGGGGGGCGCCGGACG T G TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1652014..1652142 26863196 MeRIP-seq:(Medium) rs1390491181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3580064,Human_RBP_ID_8232957,Human_RBP_ID_8728251,Human_RBP_ID_18461583,Human_RBP_ID_26783936 RMVar_hsa_circ_99682,RMVar_hsa_circ_191107 80469 RMVar_ID_80469 Human_SNP_ID_655496652 m1A Human chr19 - 1652246 1652246 1652246 GGGCGCGCCCGGTACCCCCGTGCTTTGTGCCCAGGGAACCCCGGCCCGCCCCGCGCGCGCTTGTT GGGCGCGCCCGGTACCCCCGTGCTTTGTGCCCGGGGAACCCCGGCCCGCCCCGCGCGCGCTTGTT T C TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1652245..1652622 26863196 MeRIP-seq:(Medium) rs1378912826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5238333 RMVar_hsa_circ_99682,RMVar_hsa_circ_191107 80470 RMVar_ID_80470 Human_SNP_ID_655496754 m1A Human chr19 - 1652378 1652378 1652378 ACGCGCGACCCTCGGGGGCCCGGCCGCGACGCACCTTTGTCCGGGGGGGGGCCCCCCCGCTTCAT ACGCGCGACCCTCGGGGGCCCGGCCGCGACGCCCCTTTGTCCGGGGGGGGGCCCCCCCGCTTCAT T G TCF3 Ensembl:ENSG00000071564 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1652376..1652580 26863196 MeRIP-seq:(Medium) rs989238008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558963,Human_RBP_ID_9328129,Human_RBP_ID_18191645,Human_RBP_ID_22476340 Human_Splice_Rec_1933533,Human_Splice_Rec_1933573,Human_Splice_Rec_1933609,Human_Splice_Rec_1933663,Human_Splice_Rec_1933737 80471 RMVar_ID_80471 Human_SNP_ID_655496759 m1A Human chr19 - 1652382 1652382 1652382 GCCCACGCGCGACCCTCGGGGGCCCGGCCGCGACGCACCTTTGTCCGGGGGGGGGCCCCCCCGCT GCCCACGCGCGACCCTCGGGGGCCCGGCCGCGGCGCACCTTTGTCCGGGGGGGGGCCCCCCCGCT T C TCF3 Ensembl:ENSG00000071564 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1652344..1652602 26863196 MeRIP-seq:(Medium) rs1171462220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9328129,Human_RBP_ID_18191645,Human_RBP_ID_22476340 Human_Splice_Rec_1933533,Human_Splice_Rec_1933573,Human_Splice_Rec_1933609,Human_Splice_Rec_1933663,Human_Splice_Rec_1933737 80472 RMVar_ID_80472 Human_SNP_ID_655496828 m1A Human chr19 - 1652504 1652504 1652504 GGCACCGCGGGCACCGCGCACGCCGCTGCCCCAGGGGCGCCCCGGCCGGCCGCGCGCACGGGCCC GGCACCGCGGGCACCGCGCACGCCGCTGCCCCGGGGGCGCCCCGGCCGGCCGCGCGCACGGGCCC T C TCF3 Ensembl:ENSG00000071564 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,H2O2 treatment;HEK293T,Starvation treatment chr19:1652405..1652555;chr19:1652406..1652576 26863410 MeRIP-seq:(Medium) rs1423179453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4507964,Human_RBP_ID_5238334,Human_RBP_ID_22447133 80473 RMVar_ID_80473 Human_SNP_ID_655496854 m1A Human chr19 - 1652552 1652552 1652552 CAGCGGCGGCGGCTGCGGGCGTAGCGGGCCGGAGCCGACGCGGCGGCGGGCACCGCGGGCACCGC CAGCGGCGGCGGCTGCGGGCGTAGCGGGCCGGGGCCGACGCGGCGGCGGGCACCGCGGGCACCGC T C TCF3 Ensembl:ENSG00000071564 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1652256..1652625 26863196 MeRIP-seq:(Medium) rs1233285161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557019,Human_RBP_ID_8195296,Human_RBP_ID_9293156,Human_RBP_ID_9329420,Human_RBP_ID_18421144,Human_RBP_ID_22447133 80474 RMVar_ID_80474 Human_SNP_ID_655496855 m1A Human chr19 - 1652552 1652552 1652552 CAGCGGCGGCGGCTGCGGGCGTAGCGGGCCGGAGCCGACGCGGCGGCGGGCACCGCGGGCACCGC CAGCGGCGGCGGCTGCGGGCGTAGCGGGCCGGCGCCGACGCGGCGGCGGGCACCGCGGGCACCGC T G TCF3 Ensembl:ENSG00000071564 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1652256..1652625 26863196 MeRIP-seq:(Medium) rs1233285161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557019,Human_RBP_ID_8195296,Human_RBP_ID_9293156,Human_RBP_ID_9329420,Human_RBP_ID_18421144,Human_RBP_ID_22447133 80475 RMVar_ID_80475 Human_SNP_ID_655496870 m1A Human chr19 + 1652571 1652571 1652571 CCGCCGCGTCGGCTCCGGCCCGCTACGCCCGCAGCCGCCGCCGCTGCCTCATCTTCCTGCGGCGG CCGCCGCGTCGGCTCCGGCCCGCTACGCCCGCGGCCGCCGCCGCTGCCTCATCTTCCTGCGGCGG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:1652484..1652617 26863410 MeRIP-seq:(Medium) rs1010728864 Functional Loss SNV dbSNP153 33..33 33 - - - 80476 RMVar_ID_80476 Human_SNP_ID_655550808 m1A Human chr19 - 1811458 1811458 1811458 GGGTGAGGACGGGTGCATCGGGTGGCCGGAACACAGGGGCAGGGGCTTGGCGGGGAGGGCACTGC GGGTGAGGACGGGTGCATCGGGTGGCCGGAACCCAGGGGCAGGGGCTTGGCGGGGAGGGCACTGC T G ATP8B3 Ensembl:ENSG00000130270 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1811456..1811545 26863196 MeRIP-seq:(Medium) rs1260265983 Functional Loss SNV dbSNP153 33..33 33 - - - 80477 RMVar_ID_80477 Human_SNP_ID_655552030 m1A Human chr19 - 1815363 1815363 1815363 TAGCCCCAGGGTCTGCCGTCTAGAGGGAGCCCACCGGCCTCCGGACACTGTCTTCCCGCTAGAGC TAGCCCCAGGGTCTGCCGTCTAGAGGGAGCCCGCCGGCCTCCGGACACTGTCTTCCCGCTAGAGC T C REXO1 Ensembl:ENSG00000079313 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1815313..1815433;chr19:1815315..1815434 26863196 MeRIP-seq:(Medium) rs1456585423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515979,Human_RBP_ID_5144856,Human_RBP_ID_22231407 Human_miRNA_ID_1703446 80478 RMVar_ID_80478 Human_SNP_ID_655552049 m1A Human chr19 - 1815413 1815413 1815413 CGCCCCACCCCTGCACTCCGTGACCTCTGAGAACCCAGCTGGCCCCTCGTTAGCCCCAGGGTCTG CGCCCCACCCCTGCACTCCGTGACCTCTGAGAGCCCAGCTGGCCCCTCGTTAGCCCCAGGGTCTG T C REXO1 Ensembl:ENSG00000079313 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1815347..1815774 32194978 MeRIP-seq:(Medium) rs1023308808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13393215,Human_RBP_ID_17917037,Human_RBP_ID_27465233 80479 RMVar_ID_80479 Human_SNP_ID_655552345 m1A Human chr19 - 1816012 1816012 1816012 CCTCTCCTGCCGTCCCGCTGGTCCTTAGCCCCATGCCTCTTCCAAAACAGTGCAATAAATCTCCG CCTCTCCTGCCGTCCCGCTGGTCCTTAGCCCCGTGCCTCTTCCAAAACAGTGCAATAAATCTCCG T C REXO1 Ensembl:ENSG00000079313 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1815966..1816059 26863196 MeRIP-seq:(Medium) rs1380635031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5117645,Human_RBP_ID_5192578,Human_RBP_ID_17387101,Human_RBP_ID_17502368,Human_RBP_ID_18724408,Human_RBP_ID_18946172 Human_miRNA_ID_2493917,Human_miRNA_ID_2648606,Human_miRNA_ID_2671202,Human_miRNA_ID_3101853 RMVar_hsa_circ_191119,RMVar_hsa_circ_94906 80480 RMVar_ID_80480 Human_SNP_ID_655552401 m1A Human chr19 - 1816104 1816104 1816104 GCGAGGACGCCGGCGCCTGCATGCACCTGGTGATCTGGAAGGTTCGAGAAGACGCCAAGACCAAG GCGAGGACGCCGGCGCCTGCATGCACCTGGTGCTCTGGAAGGTTCGAGAAGACGCCAAGACCAAG T G REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1815895..1816146 32194978 MeRIP-seq:(Medium) rs780290937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515993,Human_RBP_ID_8479651,Human_RBP_ID_13393232 Human_Splice_Rec_1934104,Human_Splice_Rec_1934122,Human_Splice_Rec_1934144,Human_Splice_Rec_1934146 RMVar_hsa_circ_191119,RMVar_hsa_circ_94906 80481 RMVar_ID_80481 Human_SNP_ID_655553187 m1A Human chr19 + 1817780 1817780 1817780 AGCACATGTACTGGGTCTCCCAGCCTCCGGCCACTGCAGGGGACACAGACACACAGTCAGGGCCC AGCACATGTACTGGGTCTCCCAGCCTCCGGCCGCTGCAGGGGACACAGACACACAGTCAGGGCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1817735..1820306 32194978 MeRIP-seq:(Medium) rs1401356455 Functional Loss SNV dbSNP153 33..33 33 - - - 80482 RMVar_ID_80482 Human_SNP_ID_655555485 m1A Human chr19 - 1823737 1823737 1823737 GGGGTCCCGCGGTGCCCCCGGCCCGGCCCCCGACGGCGCAGGAGGTGTGCTACCTGCGGGCCCAG GGGGTCCCGCGGTGCCCCCGGCCCGGCCCCCGGCGGCGCAGGAGGTGTGCTACCTGCGGGCCCAG T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1823658..1823757 26863410 MeRIP-seq:(Medium) rs1427460352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8838891,Human_RBP_ID_22501903 Human_Splice_Rec_1934080 80483 RMVar_ID_80483 Human_SNP_ID_655556678 m1A Human chr19 - 1826896 1826896 1826896 AACGAGTCCACCAGCGTCAAGACGGAGGACAGAGGCCGGCTGGCCCGGCAGGTGAGGCGCGCGGG AACGAGTCCACCAGCGTCAAGACGGAGGACAGGGGCCGGCTGGCCCGGCAGGTGAGGCGCGCGGG T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1826880..1826997 26863196 MeRIP-seq:(Medium) rs1357477854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241125,Human_RBP_ID_824555,Human_RBP_ID_910046,Human_RBP_ID_5526747,Human_RBP_ID_9381553,Human_RBP_ID_18995816 Human_Splice_Rec_1934077 RMVar_hsa_circ_360870 80484 RMVar_ID_80484 Human_SNP_ID_655556885 m1A Human chr19 - 1827180 1827180 1827180 GTGAGGACGAGGCCGCAGGGCCAGGGGTGCCGAGCGTGTGGCCCTCTGCCCTCCCCAGCCTCAGC GTGAGGACGAGGCCGCAGGGCCAGGGGTGCCGGGCGTGTGGCCCTCTGCCCTCCCCAGCCTCAGC T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1827131..1827214 26863196 MeRIP-seq:(Medium) rs1023466098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1556415,Human_RBP_ID_8838892,Human_RBP_ID_9294029 RMVar_hsa_circ_360870 80485 RMVar_ID_80485 Human_SNP_ID_655557105 m1A Human chr19 - 1827528 1827528 1827528 AGCCCCGTGCGGACAAGAAGGGCCCGCAGGCCAGCAGCCCCCGGCGCAAGGCAGAGCGGCCGGAA AGCCCCGTGCGGACAAGAAGGGCCCGCAGGCCGGCAGCCCCCGGCGCAAGGCAGAGCGGCCGGAA T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1827478..1827617;chr19:1827338..1827691 26863196 MeRIP-seq:(Medium) rs1454697904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22718668 RMVar_hsa_circ_360870 80486 RMVar_ID_80486 Human_SNP_ID_655557152 m1A Human chr19 - 1827591 1827591 1827591 GCAAAGACGGGGCCCAGGGGAAGGACAAGACCAAGGACAAGGGCCGAGGGCGGCCTGTGGAGAAG GCAAAGACGGGGCCCAGGGGAAGGACAAGACCGAGGACAAGGGCCGAGGGCGGCCTGTGGAGAAG T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1827304..1827844 26863196 MeRIP-seq:(Medium) rs779372013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293158 RMVar_hsa_circ_360870 80487 RMVar_ID_80487 Human_SNP_ID_655557265 m1A Human chr19 - 1827771 1827771 1827771 CCGAGGGGGGCGGCCTGCGGGAGACCAAGGAGACGGCCGTGCAGTGCGACGTGGGGGACCTCCAG CCGAGGGGGGCGGCCTGCGGGAGACCAAGGAGGCGGCCGTGCAGTGCGACGTGGGGGACCTCCAG T C REXO1 Ensembl:ENSG00000079313 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1827720..1827835 26863196 MeRIP-seq:(Medium) rs1242475501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516017 RMVar_hsa_circ_360870 80488 RMVar_ID_80488 Human_SNP_ID_655561507 m1A Human chr19 + 1840637 1840637 1840637 CCAGTAATCCTGTGTTTGGAAACACTCGCCCCACCCCCCTGCAACTCTGAGTGACACCCGGGCCC CCAGTAATCCTGTGTTTGGAAACACTCGCCCCCCCCCCCTGCAACTCTGAGTGACACCCGGGCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1840590..1840756 26863196 MeRIP-seq:(Medium) rs971410943 Functional Loss SNV dbSNP153 33..33 33 - - - 80489 RMVar_ID_80489 Human_SNP_ID_655564181 m1A Human chr19 + 1848666 1848666 1848666 CTGCCCTGCCTGCGGTCTCCGGGAGCCTCGCCAGCGCCGCCGCCCGACCTTCGGCGGCTGTAGCG CTGCCCTGCCTGCGGTCTCCGGGAGCCTCGCCGGCGCCGCCGCCCGACCTTCGGCGGCTGTAGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1848503..1848679 26863196 MeRIP-seq:(Medium) rs1023143836 Functional Loss SNV dbSNP153 33..33 33 - - - 80490 RMVar_ID_80490 Human_SNP_ID_655565523 m1A Human chr19 + 1853097 1853097 1853097 ATTCCAGGCTGGGGGTCCTCAATACCCCCCCCAAGAGGAAATGCAACCCAGGCCACAGCAGGACG ATTCCAGGCTGGGGGTCCTCAATACCCCCCCCTAGAGGAAATGCAACCCAGGCCACAGCAGGACG A T AC012615.3 Ensembl:ENSG00000267125 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1853050..1853163 26863196 MeRIP-seq:(Medium) rs1353445598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589387 80491 RMVar_ID_80491 Human_SNP_ID_655565558 m1A Human chr19 + 1853206 1853206 1853206 CACCCCACCCAAGTTCAGCTCAGAGACCCCCCACACACACTCACACCCCCTGAGGATGCCGGACC CACCCCACCCAAGTTCAGCTCAGAGACCCCCCCCACACACTCACACCCCCTGAGGATGCCGGACC A C AC012615.3 Ensembl:ENSG00000267125 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1853155..1853234 26863196 MeRIP-seq:(Medium) rs550342319 Functional Loss SNV dbSNP153 33..33 33 - - - 80492 RMVar_ID_80492 Human_SNP_ID_655565697 m1A Human chr19 - 1853622 1853622 1853622 GGTGGGTGAGAGAGGCTGCAGGGGAGGCTGGCACCGGGCTTGGGCCTCCAGTCCCTGCCTTGCTG GGTGGGTGAGAGAGGCTGCAGGGGAGGCTGGCGCCGGGCTTGGGCCTCCAGTCCCTGCCTTGCTG T C KLF16 Ensembl:ENSG00000129911 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1853574..1853655 26863196 MeRIP-seq:(Medium) rs1236223559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4510345,Human_RBP_ID_5144863,Human_RBP_ID_5238341,Human_RBP_ID_5319847,Human_RBP_ID_8195320,Human_RBP_ID_18460999,Human_RBP_ID_22371017,Human_RBP_ID_22719678,Human_RBP_ID_23786608,Human_RBP_ID_26471612,Human_RBP_ID_27465396 80493 RMVar_ID_80493 Human_SNP_ID_655566051 m1A Human chr19 + 1854521 1854521 1854521 GGGGCTGGGCGCAGGGCTCCCGGCCAGGCTGCAGGGCAGCGAGTCGCTGGGGGAGGTACTGCGGG GGGGCTGGGCGCAGGGCTCCCGGCCAGGCTGCTGGGCAGCGAGTCGCTGGGGGAGGTACTGCGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1854473..1854587 26863196 MeRIP-seq:(Medium) rs762858236 Functional Loss SNV dbSNP153 33..33 33 - - - 80494 RMVar_ID_80494 Human_SNP_ID_655566071 m1A Human chr19 - 1854548 1854548 1854548 ACCCGGACCTGCTCCGGCGCCCTGGTGCCCGCAGTACCTCCCCCAGCGACTCGCTGCCCTGCAGC ACCCGGACCTGCTCCGGCGCCCTGGTGCCCGCGGTACCTCCCCCAGCGACTCGCTGCCCTGCAGC T C KLF16 Ensembl:ENSG00000129911 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1853875..1862795 32194978 MeRIP-seq:(Medium) rs1472872608 Functional Loss SNV dbSNP153 33..33 33 - - - 80495 RMVar_ID_80495 Human_SNP_ID_655566081 m1A Human chr19 + 1854558 1854558 1854558 AGCGAGTCGCTGGGGGAGGTACTGCGGGCACCAGGGCGCCGGAGCAGGTCCGGGTGGAAGCCGGG AGCGAGTCGCTGGGGGAGGTACTGCGGGCACCGGGGCGCCGGAGCAGGTCCGGGTGGAAGCCGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1854324..1854665 26863196 MeRIP-seq:(Medium) rs3746045 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 80496 RMVar_ID_80496 Human_SNP_ID_655567726 m1A Human chr19 + 1859324 1859324 1859324 AGCAAGGGATCAGAAACCTGGCAGGCACTCAGACACTCCTCTGCACACCTCGTCCTGAGGAGTCT AGCAAGGGATCAGAAACCTGGCAGGCACTCAGGCACTCCTCTGCACACCTCGTCCTGAGGAGTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1859322..1859563 26863196 MeRIP-seq:(Medium) rs1260641866 Functional Loss SNV dbSNP153 33..33 33 - - - 80497 RMVar_ID_80497 Human_SNP_ID_655569183 m1A Human chr19 - 1863228 1863228 1863228 GCCGCCAGCATCCTGGCCGACCTGCGCGGCGGACCCGGAGCCGCCCCGGGGGGCGCCTCGCCCGC GCCGCCAGCATCCTGGCCGACCTGCGCGGCGGGCCCGGAGCCGCCCCGGGGGGCGCCTCGCCCGC T C KLF16 Ensembl:ENSG00000129911 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1863130..1863252 26863196 MeRIP-seq:(Medium) rs536381258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557025 80498 RMVar_ID_80498 Human_SNP_ID_655569215 m1A Human chr19 - 1863324 1863324 1863324 CGCGAGGCCGCCTCACCCGGGACCCCGGGGCCACCCCCGCCGCCCCCCGCCGCTTCTGGCCCGGG CGCGAGGCCGCCTCACCCGGGACCCCGGGGCCCCCCCCGCCGCCCCCCGCCGCTTCTGGCCCGGG T G KLF16 Ensembl:ENSG00000129911 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1863316..1863443 26863196 MeRIP-seq:(Medium) rs893620569 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4557026 80499 RMVar_ID_80499 Human_SNP_ID_655569239 m1A Human chr19 - 1863400 1863400 1863400 CGCCGTGGTGCACCGCGGGCGGCCCGGCCCCGAGGGCGCGGGCCCCGCCGCCGGCCTGGATGTGC CGCCGTGGTGCACCGCGGGCGGCCCGGCCCCGGGGGCGCGGGCCCCGCCGCCGGCCTGGATGTGC T C KLF16 Ensembl:ENSG00000129911 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1863358..1863571 26863196 MeRIP-seq:(Medium) rs1044970112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516262,Human_RBP_ID_773840,Human_RBP_ID_4557844,Human_RBP_ID_5320928 80500 RMVar_ID_80500 Human_SNP_ID_655574149 m1A Human chr19 - 1877409 1877409 1877409 CACGACCCTCCCGCAGCATCGAGAAGGTGTCCAAGATCACGTCTCCCGTGCTCATCATCCACGGC CACGACCCTCCCGCAGCATCGAGAAGGTGTCCTAGATCACGTCTCCCGTGCTCATCATCCACGGC T A ABHD17A Ensembl:ENSG00000129968 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1877358..1877591 32194978 MeRIP-seq:(Medium) rs1452865008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26985519 Human_Splice_Rec_1934202,Human_Splice_Rec_1934212,Human_Splice_Rec_1934216,Human_Splice_Rec_1934222,Human_Splice_Rec_1934228,Human_Splice_Rec_1934234 80501 RMVar_ID_80501 Human_SNP_ID_655574150 m1A Human chr19 - 1877409 1877409 1877409 CACGACCCTCCCGCAGCATCGAGAAGGTGTCCAAGATCACGTCTCCCGTGCTCATCATCCACGGC CACGACCCTCCCGCAGCATCGAGAAGGTGTCCGAGATCACGTCTCCCGTGCTCATCATCCACGGC T C ABHD17A Ensembl:ENSG00000129968 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1877358..1877591 32194978 MeRIP-seq:(Medium) rs1452865008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26985519 Human_Splice_Rec_1934202,Human_Splice_Rec_1934212,Human_Splice_Rec_1934216,Human_Splice_Rec_1934222,Human_Splice_Rec_1934228,Human_Splice_Rec_1934234 80502 RMVar_ID_80502 Human_SNP_ID_655574611 m1A Human chr19 + 1878706 1878706 1878706 AAGGATGCTGCCTGGCTGGTGCCTGTGGCTCCAGCTCTGCCTCGGCCTCCCTGGCCTGCTCCCTG AAGGATGCTGCCTGGCTGGTGCCTGTGGCTCCCGCTCTGCCTCGGCCTCCCTGGCCTGCTCCCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1878664..1878729 26863196 MeRIP-seq:(Medium) rs1425104439 Functional Loss SNV dbSNP153 33..33 33 - - - 80503 RMVar_ID_80503 Human_SNP_ID_655574612 m1A Human chr19 + 1878706 1878706 1878706 AAGGATGCTGCCTGGCTGGTGCCTGTGGCTCCAGCTCTGCCTCGGCCTCCCTGGCCTGCTCCCTG AAGGATGCTGCCTGGCTGGTGCCTGTGGCTCCGGCTCTGCCTCGGCCTCCCTGGCCTGCTCCCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1878664..1878729 26863196 MeRIP-seq:(Medium) rs1425104439 Functional Loss SNV dbSNP153 33..33 33 - - - 80504 RMVar_ID_80504 Human_SNP_ID_655574773 m1A Human chr19 + 1879269 1879269 1879269 CGAGACAGGCCCAGTGGATGGTGAGCAGGAAAAGCCACCAGAGGCCCACCCGGGTCTCCTCGTCC CGAGACAGGCCCAGTGGATGGTGAGCAGGAAAGGCCACCAGAGGCCCACCCGGGTCTCCTCGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr19:1879227..1879292;chr19:1879233..1879323;chr19:1879137..1879337 26863196,32194978 MeRIP-seq:(Medium) rs1407580967 Functional Loss SNV dbSNP153 33..33 33 - - - 80505 RMVar_ID_80505 Human_SNP_ID_655575170 m1A Human chr19 + 1880594 1880594 1880594 GCTGCTGGCAGGGCTATCTCCCCTCACCTCACAGAATGGTGCCCTCACTGTTGGGGCACAACTGG GCTGCTGGCAGGGCTATCTCCCCTCACCTCACGGAATGGTGCCCTCACTGTTGGGGCACAACTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1880585..1880722 26863196 MeRIP-seq:(Medium) rs1426349815 Functional Loss SNV dbSNP153 33..33 33 - - - 80506 RMVar_ID_80506 Human_SNP_ID_655575587 m1A Human chr19 - 1881563 1881563 1881563 GTGGAGGCCCGGCCTGGGCGGCGCCCGCCATGAATGGGCTGTCGCTGAGTGAGCTCTGCTGCCTC GTGGAGGCCCGGCCTGGGCGGCGCCCGCCATGTATGGGCTGTCGCTGAGTGAGCTCTGCTGCCTC T A ABHD17A Ensembl:ENSG00000129968 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1881400..1881700 32194978 MeRIP-seq:(Medium) rs765049029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516469,Human_RBP_ID_4557029,Human_RBP_ID_5319859,Human_RBP_ID_9329430 RMVar_hsa_circ_93412,RMVar_hsa_circ_191123 80507 RMVar_ID_80507 Human_SNP_ID_655575597 m1A Human chr19 + 1881581 1881581 1881581 CAGCGACAGCCCATTCATGGCGGGCGCCGCCCAGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA CAGCGACAGCCCATTCATGGCGGGCGCCGCCCGGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1881500..1881700;chr19:1881523..1881681;chr19:1881507..1881682;chr19:1881516..1881689 26863196 MeRIP-seq:(Medium) rs1358651175 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 80508 RMVar_ID_80508 Human_SNP_ID_655575598 m1A Human chr19 + 1881581 1881581 1881581 CAGCGACAGCCCATTCATGGCGGGCGCCGCCCAGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA CAGCGACAGCCCATTCATGGCGGGCGCCGCCCCGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1881500..1881700;chr19:1881523..1881681;chr19:1881507..1881682;chr19:1881516..1881689 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 80509 RMVar_ID_80509 Human_SNP_ID_655575714 m1A Human chr19 + 1881853 1881853 1881853 ACATGTGGGGTCCTTTGGGGGTGCCACAGTCCAGCTGGGCACCCCCGGGAGGCGGGGCATCCACC ACATGTGGGGTCCTTTGGGGGTGCCACAGTCCGGCTGGGCACCCCCGGGAGGCGGGGCATCCACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1881849..1881950 26863196 MeRIP-seq:(Medium) rs187860607 Functional Loss SNV dbSNP153 33..33 33 - - - 80510 RMVar_ID_80510 Human_SNP_ID_655575777 m1A Human chr19 - 1881998 1881998 1881998 AGGGAAGGTGGGGGTTCCTTCATCCTGTGGAGAGGGGGCTGAATTGGGGTCCCCTGAGCTGTAGG AGGGAAGGTGGGGGTTCCTTCATCCTGTGGAGTGGGGGCTGAATTGGGGTCCCCTGAGCTGTAGG T A ABHD17A Ensembl:ENSG00000129968 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1881949..1882050 32194978 MeRIP-seq:(Medium) rs531774300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909087,Human_RBP_ID_3582472,Human_RBP_ID_8099464,Human_RBP_ID_18165407,Human_RBP_ID_18489059,Human_RBP_ID_21978841,Human_RBP_ID_22741472,Human_RBP_ID_26335064 80511 RMVar_ID_80511 Human_SNP_ID_655576334 m1A Human chr19 + 1883968 1883968 1883968 TCTCACACCCTGCCACTCCTGGCTCCCTCAAGACAAGCCAAATTGCCCCTTCCTGCCTCTGCTCC TCTCACACCCTGCCACTCCTGGCTCCCTCAAGCCAAGCCAAATTGCCCCTTCCTGCCTCTGCTCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1883917..1884050 26863196 MeRIP-seq:(Medium) rs1241222537 Functional Loss SNV dbSNP153 33..33 33 - - - 80512 RMVar_ID_80512 Human_SNP_ID_655576348 m1A Human chr19 - 1884017 1884017 1884017 GGTTGGGCAAGGCTGTCTAGTGAGGTTGGGGAAGGGAGTTCCTGGCAGAGGAGCAGAGGCAGGAA GGTTGGGCAAGGCTGTCTAGTGAGGTTGGGGAGGGGAGTTCCTGGCAGAGGAGCAGAGGCAGGAA T C ABHD17A Ensembl:ENSG00000129968 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:1883619..1884126;chr19:1883616..1884120 26863196 MeRIP-seq:(Medium) rs7250218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263049,Human_RBP_ID_906982,Human_RBP_ID_3580105,Human_RBP_ID_5146091,Human_RBP_ID_5320946,Human_RBP_ID_8099481,Human_RBP_ID_8195361,Human_RBP_ID_8233325,Human_RBP_ID_9425679,Human_RBP_ID_17207582,Human_RBP_ID_18461605,Human_RBP_ID_18491598,Human_RBP_ID_18944653,Human_RBP_ID_22664350,Human_RBP_ID_23786897,Human_RBP_ID_24374413,Human_RBP_ID_26769743 80513 RMVar_ID_80513 Human_SNP_ID_655576625 m1A Human chr19 - 1885033 1885033 1885033 TCTTTTGCCCCGAAACTGCCCCCAGTCCGACAAACGCTTCGGCCTCTCGCCCCCCAAGGCAGCTC TCTTTTGCCCCGAAACTGCCCCCAGTCCGACAGACGCTTCGGCCTCTCGCCCCCCAAGGCAGCTC T C ABHD17A Ensembl:ENSG00000129968 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1884890..1885129 26863196 MeRIP-seq:(Medium) rs138828571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9328162 80514 RMVar_ID_80514 Human_SNP_ID_655576788 m1A Human chr19 + 1885468 1885468 1885468 CCCTGCCCGGCCTCCTGCACCGCCACCGCCGCAGCTCCCCCCACGGACGGAAGTGAGCCTCGTTC CCCTGCCCGGCCTCCTGCACCGCCACCGCCGCGGCTCCCCCCACGGACGGAAGTGAGCCTCGTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1885325..1885525 26863196 MeRIP-seq:(Medium) rs1021306090 Functional Loss SNV dbSNP153 33..33 33 - - - 80515 RMVar_ID_80515 Human_SNP_ID_655583674 m1A Human chr19 - 1905432 1905432 1905432 CGAGACCTCGGGGCCGCGCGCTTACCTGAGGGATCCGGGCGCGAGCGCAGCGCTTCGCCAAGTCT CGAGACCTCGGGGCCGCGCGCTTACCTGAGGGTTCCGGGCGCGAGCGCAGCGCTTCGCCAAGTCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1905420..1905548 26863196 MeRIP-seq:(Medium) rs1330313627 Functional Loss SNV dbSNP153 33..33 33 - - - 80516 RMVar_ID_80516 Human_SNP_ID_655583677 m1A Human chr19 - 1905436 1905436 1905436 AACCCGAGACCTCGGGGCCGCGCGCTTACCTGAGGGATCCGGGCGCGAGCGCAGCGCTTCGCCAA AACCCGAGACCTCGGGGCCGCGCGCTTACCTGGGGGATCCGGGCGCGAGCGCAGCGCTTCGCCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1905409..1905499 26863196 MeRIP-seq:(Medium) rs1013002197 Functional Loss SNV dbSNP153 33..33 33 - - - 80517 RMVar_ID_80517 Human_SNP_ID_655583680 m1A Human chr19 + 1905438 1905438 1905438 GGCGAAGCGCTGCGCTCGCGCCCGGATCCCTCAGGTAAGCGCGCGGCCCCGAGGTCTCGGGTTCT GGCGAAGCGCTGCGCTCGCGCCCGGATCCCTCCGGTAAGCGCGCGGCCCCGAGGTCTCGGGTTCT A C SCAMP4,ADAT3 Ensembl:ENSG00000227500,Ensembl:ENSG00000213638 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:1905433..1905559;chr19:1905413..1905549;chr19:1905419..1905509 26863196 MeRIP-seq:(Medium) rs908294340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557031,Human_RBP_ID_18995818,Human_RBP_ID_19088482,Human_RBP_ID_22069405 Human_Splice_Rec_1934235,Human_Splice_Rec_1934243,Human_Splice_Rec_1934253,Human_Splice_Rec_1934263,Human_Splice_Rec_1934273,Human_Splice_Rec_1934285,Human_Splice_Rec_1934327 RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 80518 RMVar_ID_80518 Human_SNP_ID_655583681 m1A Human chr19 + 1905438 1905438 1905438 GGCGAAGCGCTGCGCTCGCGCCCGGATCCCTCAGGTAAGCGCGCGGCCCCGAGGTCTCGGGTTCT GGCGAAGCGCTGCGCTCGCGCCCGGATCCCTCGGGTAAGCGCGCGGCCCCGAGGTCTCGGGTTCT A G SCAMP4,ADAT3 Ensembl:ENSG00000227500,Ensembl:ENSG00000213638 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:1905433..1905559;chr19:1905413..1905549;chr19:1905419..1905509 26863196 MeRIP-seq:(Medium) rs908294340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557031,Human_RBP_ID_18995818,Human_RBP_ID_19088482,Human_RBP_ID_22069405 Human_Splice_Rec_1934235,Human_Splice_Rec_1934243,Human_Splice_Rec_1934253,Human_Splice_Rec_1934263,Human_Splice_Rec_1934273,Human_Splice_Rec_1934285,Human_Splice_Rec_1934327 RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 80519 RMVar_ID_80519 Human_SNP_ID_655586731 m1A Human chr19 - 1912928 1912928 1912928 CGCGGGTCACGTACAGGTCGTAGCCAGTGCACAGGTAGGGGAGGCCGTCCTCGTCTGCGTCCAGT CGCGGGTCACGTACAGGTCGTAGCCAGTGCACGGGTAGGGGAGGCCGTCCTCGTCTGCGTCCAGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1912926..1913056 32194978 MeRIP-seq:(Medium) rs767469574 Functional Loss SNV dbSNP153 33..33 33 - - - 80520 RMVar_ID_80520 Human_SNP_ID_655586829 m1A Human chr19 - 1913045 1913045 1913045 CGGGCCGTGCGTGGATGCGGAAGCGGGTGCCCAGGGCGCCGTCGGGCGAGGGCGCACCGTAGAAG CGGGCCGTGCGTGGATGCGGAAGCGGGTGCCCTGGGCGCCGTCGGGCGAGGGCGCACCGTAGAAG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1913032..1913215 26863196 MeRIP-seq:(Medium) rs113371893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23130843 80521 RMVar_ID_80521 Human_SNP_ID_655586830 m1A Human chr19 - 1913045 1913045 1913045 CGGGCCGTGCGTGGATGCGGAAGCGGGTGCCCAGGGCGCCGTCGGGCGAGGGCGCACCGTAGAAG CGGGCCGTGCGTGGATGCGGAAGCGGGTGCCCGGGGCGCCGTCGGGCGAGGGCGCACCGTAGAAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1913032..1913215 26863196 MeRIP-seq:(Medium) rs113371893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23130843 80522 RMVar_ID_80522 Human_SNP_ID_655591466 m1A Human chr19 - 1924407 1924407 1924407 CCCTGGCAGGAGGGGGGCGGTCCGTGGCCACCACCGGCTTCCACCATCCCAGCTGGGGGGATGGG CCCTGGCAGGAGGGGGGCGGTCCGTGGCCACCGCCGGCTTCCACCATCCCAGCTGGGGGGATGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1924375..1924447 26863196 MeRIP-seq:(Medium) rs1014713523 Functional Loss SNV dbSNP153 33..33 33 - - - 80523 RMVar_ID_80523 Human_SNP_ID_655592003 m1A Human chr19 - 1925816 1925816 1925816 CCTCTTGGCAGACTGGCCGGGGGCAGGACCTGAAGACCCTGAAGCATGGCCGTGAGACCCATGGG CCTCTTGGCAGACTGGCCGGGGGCAGGACCTGGAGACCCTGAAGCATGGCCGTGAGACCCATGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1925366..1925963 32194978 MeRIP-seq:(Medium) rs1220983103 Functional Loss SNV dbSNP153 33..33 33 - - - 80524 RMVar_ID_80524 Human_SNP_ID_655597383 m1A Human chr19 - 1941186 1941186 1941186 CCGCCGCGCCCGCTCCGGGGCCCGCGCGCCTTACGCCGCCAGCGTCTGCCAGCGGGGGGCGGCAG CCGCCGCGCCCGCTCCGGGGCCCGCGCGCCTTCCGCCGCCAGCGTCTGCCAGCGGGGGGCGGCAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:1941176..1941338 26863196 MeRIP-seq:(Medium) rs1422255109 Functional Loss SNV dbSNP153 33..33 33 - - - 80525 RMVar_ID_80525 Human_SNP_ID_655597448 m1A Human chr19 + 1941304 1941281 1941304 GGCGCGGGAGCCGGAGCGGGGGCCCAAGCGGCACCGGAGCCGGAGCGCGAGGGGGCGCGGGGCCC GGCGCGGGAG_______________________CCGGAGCCGGAGCGCGAGGGGGCGCGGGGCCC GCCGGAGCGGGGGCCCAAGCGGCA G CSNK1G2 Ensembl:ENSG00000133275 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1941151..1941794;chr19:1941194..1941451;chr19:1941247..1941396;chr19:1941151..1941453;chr19:1941151..1941457;chr19:1941192..1942485 26863196,26863410,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1217717264 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_4558978,Human_RBP_ID_5320954,Human_RBP_ID_9328170,Human_RBP_ID_18421151 80526 RMVar_ID_80526 Human_SNP_ID_655597589 m1A Human chr19 - 1941594 1941594 1941594 GTTGCGGCGGTGGGGCCCTGAGTGTGGGGGTCAGCTTGCGGGGCGGTTAGACGGGTTGGGGGGCG GTTGCGGCGGTGGGGCCCTGAGTGTGGGGGTCCGCTTGCGGGGCGGTTAGACGGGTTGGGGGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1941591..1941794 26863196 MeRIP-seq:(Medium) rs1420561586 Functional Loss SNV dbSNP153 33..33 33 - - - 80527 RMVar_ID_80527 Human_SNP_ID_655608491 m1A Human chr19 + 1969595 1969595 1969595 CCGAGAGCGACCCCGAGGCCACTGAGAAGAGCAGCGCGGCCTGGCCGGCCCGAACGCCTGCGTCT CCGAGAGCGACCCCGAGGCCACTGAGAAGAGCCGCGCGGCCTGGCCGGCCCGAACGCCTGCGTCT A C CSNK1G2 Ensembl:ENSG00000133275 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1969547..1969795 32194978 MeRIP-seq:(Medium) rs990237954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557037,Human_RBP_ID_18421158 Human_Splice_Rec_1934332,Human_Splice_Rec_1934354,Human_Splice_Rec_1934358,Human_Splice_Rec_1934364 RMVar_hsa_circ_286268 80528 RMVar_ID_80528 Human_SNP_ID_655611587 m1A Human chr19 + 1978558 1978558 1978558 GCGGGTGGGGCGGGGGCTGCGCAGGGGCAGGGAGGGGGCTGCCGCCGCACGCCCGTGCGTCTGTC GCGGGTGGGGCGGGGGCTGCGCAGGGGCAGGGCGGGGGCTGCCGCCGCACGCCCGTGCGTCTGTC A C CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1978412..1978615 26863196 MeRIP-seq:(Medium) rs1380756800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908240,Human_RBP_ID_3954032,Human_RBP_ID_5372605,Human_RBP_ID_18412197,Human_RBP_ID_18470377,Human_RBP_ID_18944661,Human_RBP_ID_19088490,Human_RBP_ID_21978355,Human_RBP_ID_22545292,Human_RBP_ID_23210788,Human_RBP_ID_23257406,Human_RBP_ID_26335074,Human_RBP_ID_26783482,Human_RBP_ID_27815751,Human_RBP_ID_27839141 RMVar_hsa_circ_30310,RMVar_hsa_circ_66694 80529 RMVar_ID_80529 Human_SNP_ID_655612147 m1A Human chr19 + 1979506 1979506 1979506 CCGCTGGCGCTCTCTCTGCAGAGGAGATGGCCACGTACCTGCGCTATGTGCGGCGCCTGGACTTC CCGCTGGCGCTCTCTCTGCAGAGGAGATGGCCGCGTACCTGCGCTATGTGCGGCGCCTGGACTTC A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1979326..1979575 32194978 MeRIP-seq:(Medium) rs35076486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910058 Human_Splice_Rec_1934346,Human_Splice_Rec_1934394,Human_Splice_Rec_1934400,Human_Splice_Rec_1934410,Human_Splice_Rec_1934418 RMVar_hsa_circ_30310,RMVar_hsa_circ_66694 80530 RMVar_ID_80530 Human_SNP_ID_655612190 m1A Human chr19 + 1979591 1979591 1979591 CTACCTGCGGAAGCTCTTCACCGACCTCTTCGACCGCAGTGGCTTCGTGTTCGACTATGAGTACG CTACCTGCGGAAGCTCTTCACCGACCTCTTCGGCCGCAGTGGCTTCGTGTTCGACTATGAGTACG A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1979542..1979643 26863196 MeRIP-seq:(Medium) rs1395807833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8830727,Human_RBP_ID_18191660,Human_RBP_ID_22066021,Human_RBP_ID_26814855 Human_Splice_Rec_1934346,Human_Splice_Rec_1934347,Human_Splice_Rec_1934394,Human_Splice_Rec_1934395,Human_Splice_Rec_1934400,Human_Splice_Rec_1934401,Human_Splice_Rec_1934410,Human_Splice_Rec_1934411,Human_Splice_Rec_1934418,Human_Splice_Rec_1934419 RMVar_hsa_circ_30310,RMVar_hsa_circ_66694 80531 RMVar_ID_80531 Human_SNP_ID_655612379 m1A Human chr19 + 1979923 1979923 1979923 CCCCCTACTGCCCCCACCAGGCGTTGAACTCCACCAACGGGGAGCTGAATGCGGACGACCCCACG CCCCCTACTGCCCCCACCAGGCGTTGAACTCCGCCAACGGGGAGCTGAATGCGGACGACCCCACG A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1979914..1980017 26863196 MeRIP-seq:(Medium) rs771387763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54178,Human_RBP_ID_18995832 Human_Splice_Rec_1934350,Human_Splice_Rec_1934351,Human_Splice_Rec_1934404,Human_Splice_Rec_1934405,Human_Splice_Rec_1934414,Human_Splice_Rec_1934415 RMVar_hsa_circ_30310,RMVar_hsa_circ_191128,RMVar_hsa_circ_92055,RMVar_hsa_circ_191129,RMVar_hsa_circ_308905 80532 RMVar_ID_80532 Human_SNP_ID_655612380 m1A Human chr19 + 1979923 1979923 1979923 CCCCCTACTGCCCCCACCAGGCGTTGAACTCCACCAACGGGGAGCTGAATGCGGACGACCCCACG CCCCCTACTGCCCCCACCAGGCGTTGAACTCCTCCAACGGGGAGCTGAATGCGGACGACCCCACG A T CSNK1G2 Ensembl:ENSG00000133275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1979914..1980017 26863196 MeRIP-seq:(Medium) rs771387763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54178,Human_RBP_ID_18995832 Human_Splice_Rec_1934350,Human_Splice_Rec_1934351,Human_Splice_Rec_1934404,Human_Splice_Rec_1934405,Human_Splice_Rec_1934414,Human_Splice_Rec_1934415 RMVar_hsa_circ_30310,RMVar_hsa_circ_191128,RMVar_hsa_circ_92055,RMVar_hsa_circ_191129,RMVar_hsa_circ_308905 80533 RMVar_ID_80533 Human_SNP_ID_655612731 m1A Human chr19 + 1980537 1980537 1980537 TCCTGCCCCTCCGTTTCTTTGCTGAAGTGAGTAGTGTGATCCTGGAGGCCCCCCGGCCTGGCCCC TCCTGCCCCTCCGTTTCTTTGCTGAAGTGAGTTGTGTGATCCTGGAGGCCCCCCGGCCTGGCCCC A T CSNK1G2 Ensembl:ENSG00000133275 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1980486..1980863 26863196 MeRIP-seq:(Medium) rs140393631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279323,Human_RBP_ID_517020,Human_RBP_ID_4564480,Human_RBP_ID_5115954,Human_RBP_ID_13405999,Human_RBP_ID_23787903,Human_RBP_ID_24483930,Human_RBP_ID_26471636,Human_RBP_ID_27270953 80534 RMVar_ID_80534 Human_SNP_ID_655612736 m1A Human chr19 - 1980563 1980550 1980563 ACGCTAACGGGGGCGGCTGGCGGGGCGGGGCCAGGCCGGGGGGCCTCCAGGATCACACTACTCAC ACGCTAACGGGGGCGGCTGGCGGGGCGGGGCC_____________TCCAGGATCACACTACTCAC AGGCCCCCCGGCCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1980521..1980663 26863196 MeRIP-seq:(Medium) rs1190097728 Functional Loss DEL dbSNP153 33..45 33 - - - 80535 RMVar_ID_80535 Human_SNP_ID_655612754 m1A Human chr19 - 1980563 1980563 1980563 ACGCTAACGGGGGCGGCTGGCGGGGCGGGGCCAGGCCGGGGGGCCTCCAGGATCACACTACTCAC ACGCTAACGGGGGCGGCTGGCGGGGCGGGGCCCGGCCGGGGGGCCTCCAGGATCACACTACTCAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1980521..1980663 26863196 MeRIP-seq:(Medium) rs1346985867 Functional Loss SNV dbSNP153 33..33 33 - - - 80536 RMVar_ID_80536 Human_SNP_ID_655612797 m1A Human chr19 + 1980690 1980690 1980690 GCCTGGAGGGGTGCTGTGGAGCTGTCTTGCCCAGGCCCTCCTGGGAGGGGGACAGGCATTGTTGC GCCTGGAGGGGTGCTGTGGAGCTGTCTTGCCCGGGCCCTCCTGGGAGGGGGACAGGCATTGTTGC A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1980495..1980961 26863196 MeRIP-seq:(Medium) rs1046638903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517024,Human_RBP_ID_4512615,Human_RBP_ID_17917641,Human_RBP_ID_26471638,Human_RBP_ID_27815754 80537 RMVar_ID_80537 Human_SNP_ID_655614563 m1A Human chr19 + 1985551 1985550 1985552 GCTTTGGGGAGGACGCAGGTTCCAGGAGTCACAGGGCAGAAACACGCGGGGTGGGTGGGGGCGTG GCTTTGGGGAGGACGCAGGTTCCAGGAGTCAC__GGCAGAAACACGCGGGGTGGGTGGGGGCGTG CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1985501..1985775 26863196 MeRIP-seq:(Medium) rs1010828481 Functional Loss DEL dbSNP153 33..34 33 - - - 80538 RMVar_ID_80538 Human_SNP_ID_655616901 m1A Human chr19 + 1990916 1990916 1990916 CCCAGTGCGGGGCCGGTTCAAATGCAGCCCTGACCACACGGGCCTTCCTGAGCGTGGCCAGGAGC CCCAGTGCGGGGCCGGTTCAAATGCAGCCCTGGCCACACGGGCCTTCCTGAGCGTGGCCAGGAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1990352..1990948 32194978 MeRIP-seq:(Medium) rs981562673 Functional Loss SNV dbSNP153 33..33 33 - - - 80539 RMVar_ID_80539 Human_SNP_ID_655619164 m1A Human chr19 - 1997396 1997396 1997396 CCATGTTCAACGGGGGAATGGCCACAACATCCACGGAGATTGAGCTGCCCGACGTGGAACCCGCT CCATGTTCAACGGGGGAATGGCCACAACATCCGCGGAGATTGAGCTGCCCGACGTGGAACCCGCT T C BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:1997297..1997495;chr19:1997310..1997450 26863196 MeRIP-seq:(Medium) rs1190694382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558984,Human_RBP_ID_8830759,Human_RBP_ID_17917720,Human_RBP_ID_18191678,Human_RBP_ID_18725241,Human_RBP_ID_26471644,Human_RBP_ID_26814864 Human_Splice_Rec_1934444,Human_Splice_Rec_1934445,Human_Splice_Rec_1934465,Human_Splice_Rec_1934482,Human_Splice_Rec_1934483,Human_Splice_Rec_1934490,Human_Splice_Rec_1934491,Human_Splice_Rec_1934500,Human_Splice_Rec_1934501,Human_Splice_Rec_1934506 RMVar_hsa_circ_18236,RMVar_hsa_circ_39383,RMVar_hsa_circ_288823,RMVar_hsa_circ_191131,RMVar_hsa_circ_301914 80540 RMVar_ID_80540 Human_SNP_ID_655623748 m1A Human chr19 + 2010418 2010418 2010418 CGCGTGCAACCCCTGGCCTCCTCCCCAGCACAAACGCCGACCCCTGCGCGACGGTCCAGACACTG CGCGTGCAACCCCTGGCCTCCTCCCCAGCACAGACGCCGACCCCTGCGCGACGGTCCAGACACTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2010411..2010654 26863196 MeRIP-seq:(Medium) rs930880102 Functional Loss SNV dbSNP153 33..33 33 - - - 80541 RMVar_ID_80541 Human_SNP_ID_655623787 m1A Human chr19 + 2010525 2010525 2010525 TCTCAGCTCACCCTGCACCCCCGCCAGGGACCAGGCCCAAGCCCAGGCCACTTGCTCTCCTCACA TCTCAGCTCACCCTGCACCCCCGCCAGGGACCGGGCCCAAGCCCAGGCCACTTGCTCTCCTCACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2010521..2010608 26863196 MeRIP-seq:(Medium) rs1035550701 Functional Loss SNV dbSNP153 33..33 33 - - - 80542 RMVar_ID_80542 Human_SNP_ID_655625532 m1A Human chr19 - 2015432 2015432 2015432 GGCGGGCCCGGGGGCGGCGGCGCTGCAGCGCGAGGCCGCGTACAACTGGCAGGCCAGCAAGCCCA GGCGGGCCCGGGGGCGGCGGCGCTGCAGCGCGTGGCCGCGTACAACTGGCAGGCCAGCAAGCCCA T A BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2015253..2015685 26863196 MeRIP-seq:(Medium) rs1311409535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4512835,Human_RBP_ID_5319880,Human_RBP_ID_9328181,Human_RBP_ID_18192653,Human_RBP_ID_22501999 80543 RMVar_ID_80543 Human_SNP_ID_655625556 m1A Human chr19 - 2015468 2015468 2015468 CGCGCAGGCCGCGGGCGCGGAGCGGGCGGAGGAGGCGGCGGGCCCGGGGGCGGCGGCGCTGCAGC CGCGCAGGCCGCGGGCGCGGAGCGGGCGGAGGCGGCGGCGGGCCCGGGGGCGGCGGCGCTGCAGC T G BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:2015300..2015701 26863410 MeRIP-seq:(Medium) rs1316782647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241636,Human_RBP_ID_3585117,Human_RBP_ID_4512837,Human_RBP_ID_5319880,Human_RBP_ID_9328181,Human_RBP_ID_18191680 80544 RMVar_ID_80544 Human_SNP_ID_655625574 m1A Human chr19 - 2015501 2015501 2015501 GACGCCGCCCGCCCCGCCGGGCCCCGGGACAGACGCGCAGGCCGCGGGCGCGGAGCGGGCGGAGG GACGCCGCCCGCCCCGCCGGGCCCCGGGACAGGCGCGCAGGCCGCGGGCGCGGAGCGGGCGGAGG T C BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2015244..2015698 26863196 MeRIP-seq:(Medium) rs1357376530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4512840,Human_RBP_ID_9328181,Human_RBP_ID_22533263 80545 RMVar_ID_80545 Human_SNP_ID_655625634 m1A Human chr19 - 2015585 2015585 2015585 CGCCAACGCCGCCGCCACCCCGGCCCCCGGCAACGCGGCCGCCGCCGCCGCCGCCGCCGCCGCCG CGCCAACGCCGCCGCCACCCCGGCCCCCGGCAGCGCGGCCGCCGCCGCCGCCGCCGCCGCCGCCG T C BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2015484..2015671 26863196 MeRIP-seq:(Medium) rs1293841744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5239070,Human_RBP_ID_26784217 80546 RMVar_ID_80546 Human_SNP_ID_655625638 m1A Human chr19 - 2015601 2015595 2015601 GCAGTCCCGGGCCCAGCGCCAACGCCGCCGCCACCCCGGCCCCCGGCAACGCGGCCGCCGCCGCC GCAGTCCCGGGCCCAGCGCCAACGCCGCCGCC______GCCCCCGGCAACGCGGCCGCCGCCGCC CCGGGGT C BTBD2 Ensembl:ENSG00000133243 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2015595..2015681 26863196 MeRIP-seq:(Medium) rs1237785298 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4564535,Human_RBP_ID_5239070,Human_RBP_ID_26784217 80547 RMVar_ID_80547 Human_SNP_ID_655633217 m1A Human chr19 + 2037850 2037843 2037851 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAA________AAACAAACAAACGCTGCTAGCCACTCAGCTT AAAAAAAAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs771997298 Functional Loss DEL dbSNP153 27..34 33 - - - 80548 RMVar_ID_80548 Human_SNP_ID_655633223 m1A Human chr19 + 2037850 2037846 2037851 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAAAAA_____AAACAAACAAACGCTGCTAGCCACTCAGCTT AAAAAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs754191916 Functional Loss DEL dbSNP153 30..34 33 - - - 80549 RMVar_ID_80549 Human_SNP_ID_655633231 m1A Human chr19 + 2037850 2037847 2037851 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAAAAAA____AAACAAACAAACGCTGCTAGCCACTCAGCTT AAAAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs199520689 Functional Loss DEL dbSNP153 31..34 33 - - - 80550 RMVar_ID_80550 Human_SNP_ID_655633236 m1A Human chr19 + 2037850 2037848 2037851 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAAAAAAA___AAACAAACAAACGCTGCTAGCCACTCAGCTT AAAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs748954560 Functional Loss DEL dbSNP153 32..34 33 - - - 80551 RMVar_ID_80551 Human_SNP_ID_655633238 m1A Human chr19 + 2037850 2037849 2037851 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAAAAAAAA__AAACAAACAAACGCTGCTAGCCACTCAGCTT AAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs768531523 Functional Loss DEL dbSNP153 33..34 33 - - - 80552 RMVar_ID_80552 Human_SNP_ID_655633240 m1A Human chr19 + 2037850 2037850 2037850 TGACTGTCCCACCTTCAGAAAAAAAAAAAAAAACAAACAAACAAACGCTGCTAGCCACTCAGCTT TGACTGTCCCACCTTCAGAAAAAAAAAAAAAACCAAACAAACAAACGCTGCTAGCCACTCAGCTT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2037826..2037850 32194978 MeRIP-seq:(Medium) rs778776283 Functional Loss SNV dbSNP153 33..33 33 - - - 80553 RMVar_ID_80553 Human_SNP_ID_655633350 m1A Human chr19 - 2038061 2038061 2038061 CCTTCCCTGGTCCCCACTGCCCATATCTGTGGACTGCCCCTTCCAAAGACCCCTGGGGGGGGTGG CCTTCCCTGGTCCCCACTGCCCATATCTGTGGGCTGCCCCTTCCAAAGACCCCTGGGGGGGGTGG T C MKNK2 Ensembl:ENSG00000099875 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2038011..2038260 32194978 MeRIP-seq:(Medium) rs1036029626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093794,Human_RBP_ID_17271714,Human_RBP_ID_17386538 Human_miRNA_ID_1012427,Human_miRNA_ID_1020610,Human_miRNA_ID_1294437,Human_miRNA_ID_1298413,Human_miRNA_ID_1329250 80554 RMVar_ID_80554 Human_SNP_ID_655634201 m1A Human chr19 - 2040097 2040097 2040097 GGCCCGCAGGGGTGCTCGGGACCCCTGAGTCCAGGGGGCGGGGTTTCCAGGTTAAGACATTTGTG GGCCCGCAGGGGTGCTCGGGACCCCTGAGTCCCGGGGGCGGGGTTTCCAGGTTAAGACATTTGTG T G MKNK2 Ensembl:ENSG00000099875 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2040091..2040220 26863196 MeRIP-seq:(Medium) rs372336895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909092,Human_RBP_ID_5372612,Human_RBP_ID_17917785,Human_RBP_ID_19088498,Human_RBP_ID_22664360,Human_RBP_ID_26784892 Human_Splice_Rec_1934512,Human_Splice_Rec_1934520,Human_Splice_Rec_1934544,Human_Splice_Rec_1934570,Human_Splice_Rec_1934602,Human_Splice_Rec_1934612,Human_Splice_Rec_1934632,Human_Splice_Rec_1934638,Human_Splice_Rec_1934650 80555 RMVar_ID_80555 Human_SNP_ID_655635464 m1A Human chr19 - 2042664 2042664 2042664 TCACCCCGTCGTGGTTCTGTGGCTTCTCCCCCAGGCATCGCCCACAGGGACCTAAAGCCGGAAAA TCACCCCGTCGTGGTTCTGTGGCTTCTCCCCCCGGCATCGCCCACAGGGACCTAAAGCCGGAAAA T G MKNK2 Ensembl:ENSG00000099875 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2042662..2042745 26863196 MeRIP-seq:(Medium) rs78002226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4512990,Human_RBP_ID_9381563,Human_RBP_ID_26783485 Human_Splice_Rec_1934537,Human_Splice_Rec_1934563,Human_Splice_Rec_1934573,Human_Splice_Rec_1934595,Human_Splice_Rec_1934605,Human_Splice_Rec_1934625,Human_Splice_Rec_1934643 RMVar_hsa_circ_40342,RMVar_hsa_circ_340549,RMVar_hsa_circ_191133,RMVar_hsa_circ_103486,RMVar_hsa_circ_81120,RMVar_hsa_circ_191134,RMVar_hsa_circ_82061,RMVar_hsa_circ_379066,RMVar_hsa_circ_44944,RMVar_hsa_circ_191136 80556 RMVar_ID_80556 Human_SNP_ID_655635839 m1A Human chr19 - 2043575 2043575 2043575 TGCTGTGTCCTTTCGCCTGTTTCAGATCATTGAGAAGCAGCCAGGCCACATTCGGAGCAGGGTTT TGCTGTGTCCTTTCGCCTGTTTCAGATCATTGGGAAGCAGCCAGGCCACATTCGGAGCAGGGTTT T C MKNK2 Ensembl:ENSG00000099875 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2043476..2043629 26863196 MeRIP-seq:(Medium) rs1408835472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910068,Human_RBP_ID_3954047,Human_RBP_ID_4513001,Human_RBP_ID_18995845,Human_RBP_ID_22741492,Human_RBP_ID_23788104 Human_Splice_Rec_1934530,Human_Splice_Rec_1934531,Human_Splice_Rec_1934556,Human_Splice_Rec_1934557,Human_Splice_Rec_1934588,Human_Splice_Rec_1934589,Human_Splice_Rec_1934618,Human_Splice_Rec_1934619,Human_Splice_Rec_1934639 RMVar_hsa_circ_40342,RMVar_hsa_circ_340549,RMVar_hsa_circ_45690,RMVar_hsa_circ_191133,RMVar_hsa_circ_103486,RMVar_hsa_circ_81120,RMVar_hsa_circ_191134,RMVar_hsa_circ_82061,RMVar_hsa_circ_379066,RMVar_hsa_circ_191136,RMVar_hsa_circ_45478 80557 RMVar_ID_80557 Human_SNP_ID_655636719 m1A Human chr19 - 2046426 2046423 2046426 CAGCCAGCCCATTGACATCCCGGACGCCAAGAAGAGGGGCAAGAAGAAGAAGCGCGGCCGGGCCA CAGCCAGCCCATTGACATCCCGGACGCCAAGA___GGGGCAAGAAGAAGAAGCGCGGCCGGGCCA CTCT C MKNK2 Ensembl:ENSG00000099875 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2046145..2046648 26863196 MeRIP-seq:(Medium) rs781217314 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_52939,Human_RBP_ID_910070,Human_RBP_ID_5372630,Human_RBP_ID_18993995 Human_Splice_Rec_1934526,Human_Splice_Rec_1934527,Human_Splice_Rec_1934552,Human_Splice_Rec_1934553,Human_Splice_Rec_1934584,Human_Splice_Rec_1934585,Human_Splice_Rec_1934616,Human_Splice_Rec_1934617 RMVar_hsa_circ_40342,RMVar_hsa_circ_191133,RMVar_hsa_circ_103486,RMVar_hsa_circ_81120,RMVar_hsa_circ_191134,RMVar_hsa_circ_82061,RMVar_hsa_circ_191136,RMVar_hsa_circ_67815,RMVar_hsa_circ_45478,RMVar_hsa_circ_191137,RMVar_hsa_circ_370498 80558 RMVar_ID_80558 Human_SNP_ID_655637241 m1A Human chr19 - 2047880 2047880 2047880 AGGTGTGCCGGGCAGCTGCGGGACATGGGCGGAGGAATGCAGGTGTCTGGGCTTGGGTAGGGGCA AGGTGTGCCGGGCAGCTGCGGGACATGGGCGGGGGAATGCAGGTGTCTGGGCTTGGGTAGGGGCA T C MKNK2 Ensembl:ENSG00000099875 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2047878..2047983 26863196 MeRIP-seq:(Medium) rs551049808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3580150,Human_RBP_ID_5369660,Human_RBP_ID_8099566,Human_RBP_ID_8233335,Human_RBP_ID_18489168,Human_RBP_ID_22699010,Human_RBP_ID_22718732,Human_RBP_ID_22742239,Human_RBP_ID_26759425 RMVar_hsa_circ_81120,RMVar_hsa_circ_191134,RMVar_hsa_circ_45478 80559 RMVar_ID_80559 Human_SNP_ID_655638228 m1A Human chr19 + 2050871 2050871 2050871 TCTTCTGCACCATCTTCTGTCCGGGCCCCGCCAGCGGGGGAGGGGACCGAGGGCCCGGGGGGAGG TCTTCTGCACCATCTTCTGTCCGGGCCCCGCCTGCGGGGGAGGGGACCGAGGGCCCGGGGGGAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2050826..2050979 26863196 MeRIP-seq:(Medium) rs1568241504 Functional Loss SNV dbSNP153 33..33 33 - - - 80560 RMVar_ID_80560 Human_SNP_ID_655638255 m1A Human chr19 - 2050949 2050910 2050949 TCACCGCCCTCCCTTTGTCTGCTCCCGCCCGCAGGGTCCCCTCCTCGGCCGCCCCCCGCCCGGCC TCACCGCCCTCCCTTTGTCTGCTCCCGCCCGC_________________________________ GGCGGGCGGCCGGGCGGGGGGCGGCCGAGGAGGGGACCCT G MKNK2 Ensembl:ENSG00000099875 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:2050851..2051121 26863410 MeRIP-seq:(Medium) rs1284362287 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_910073,Human_RBP_ID_19091358 80561 RMVar_ID_80561 Human_SNP_ID_655638267 m1A Human chr19 + 2050940 2050940 2050940 AGGGCGGGCGGCCGGGCGGGGGGCGGCCGAGGAGGGGACCCTGCGGGCGGGAGCAGACAAAGGGA AGGGCGGGCGGCCGGGCGGGGGGCGGCCGAGGGGGGGACCCTGCGGGCGGGAGCAGACAAAGGGA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr19:2050909..2051037;chr19:2050876..2051077 26863196,26863410 MeRIP-seq:(Medium) rs1264896653 Functional Loss SNV dbSNP153 33..33 33 - - - 80562 RMVar_ID_80562 Human_SNP_ID_655638400 m1A Human chr19 - 2051219 2051219 2051219 ACGCGCCCGGCTCCTCTCAGCGGCGGTGGCCCAGGTAGAGGGGTCCGCGCTGGCGGCGGCGGCGG ACGCGCCCGGCTCCTCTCAGCGGCGGTGGCCCTGGTAGAGGGGTCCGCGCTGGCGGCGGCGGCGG T A MKNK2 Ensembl:ENSG00000099875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2051041..2051250 26863196 MeRIP-seq:(Medium) rs1334819109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241186,Human_RBP_ID_773473,Human_RBP_ID_4557045,Human_RBP_ID_17670143,Human_RBP_ID_23130855,Human_RBP_ID_27839148 Human_Splice_Rec_1934653 80563 RMVar_ID_80563 Human_SNP_ID_655638401 m1A Human chr19 - 2051219 2051219 2051219 ACGCGCCCGGCTCCTCTCAGCGGCGGTGGCCCAGGTAGAGGGGTCCGCGCTGGCGGCGGCGGCGG ACGCGCCCGGCTCCTCTCAGCGGCGGTGGCCCGGGTAGAGGGGTCCGCGCTGGCGGCGGCGGCGG T C MKNK2 Ensembl:ENSG00000099875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2051041..2051250 26863196 MeRIP-seq:(Medium) rs1334819109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241186,Human_RBP_ID_773473,Human_RBP_ID_4557045,Human_RBP_ID_17670143,Human_RBP_ID_23130855,Human_RBP_ID_27839148 Human_Splice_Rec_1934653 80564 RMVar_ID_80564 Human_SNP_ID_655641621 m1A Human chr19 - 2061331 2061331 2061331 CGCCCAGAGCCCCGGCCGCCGGGAGGAGGAGGAGGCGGCGCCCGGGGACTGGCCTAGCGCGGGTG CGCCCAGAGCCCCGGCCGCCGGGAGGAGGAGGTGGCGGCGCCCGGGGACTGGCCTAGCGCGGGTG T A lnc-MKNK2-1 RNACentral:URS00008B93B0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2061318..2061438 26863196 MeRIP-seq:(Medium) rs1379244368 Functional Loss SNV dbSNP153 33..33 33 - - - 80565 RMVar_ID_80565 Human_SNP_ID_655641622 m1A Human chr19 - 2061331 2061331 2061331 CGCCCAGAGCCCCGGCCGCCGGGAGGAGGAGGAGGCGGCGCCCGGGGACTGGCCTAGCGCGGGTG CGCCCAGAGCCCCGGCCGCCGGGAGGAGGAGGCGGCGGCGCCCGGGGACTGGCCTAGCGCGGGTG T G lnc-MKNK2-1 RNACentral:URS00008B93B0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2061318..2061438 26863196 MeRIP-seq:(Medium) rs1379244368 Functional Loss SNV dbSNP153 33..33 33 - - - 80566 RMVar_ID_80566 Human_SNP_ID_655652276 m1A Human chr19 + 2096102 2096102 2096102 CCGTAGCCTAAGTTCGCCCGTCTGAGGGATCCAGCTTCCCCGCCGCCAGGGTTCGCCCTTCCTGA CCGTAGCCTAAGTTCGCCCGTCTGAGGGATCCTGCTTCCCCGCCGCCAGGGTTCGCCCTTCCTGA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2096099..2096258 26863196 MeRIP-seq:(Medium) rs927487221 Functional Loss SNV dbSNP153 33..33 33 - - - 80567 RMVar_ID_80567 Human_SNP_ID_655652286 m1A Human chr19 - 2096129 2096129 2096129 AACTTAGGCGGCGAGGAGACCGAGTTCTCAGGAAGGGCGAACCCTGGCGGCGGGGAAGCTGGATC AACTTAGGCGGCGAGGAGACCGAGTTCTCAGGCAGGGCGAACCCTGGCGGCGGGGAAGCTGGATC T G MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2096123..2096306 26863196 MeRIP-seq:(Medium) rs1396995689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9425067,Human_RBP_ID_13406960 RMVar_hsa_circ_118892,RMVar_hsa_circ_191141 80568 RMVar_ID_80568 Human_SNP_ID_655652306 m1A Human chr19 + 2096218 2096174 2096218 CCGCCTCTGCCGCCCGCCTTCGCCCCTCCCGGACACCCACCTGATCGCCTCTGCCGCCCGCCTTC _________________________________CACCCACCTGATCGCCTCTGCCGCCCGCCTTC GCACCCACCTGGCCGCCTCTGCCGCCCGCCTTCGCCCCTCCCGGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2096052..2096303 26863196 MeRIP-seq:(Medium) rs1568260316 Functional Loss DEL dbSNP153 1..33 33 - - - 80569 RMVar_ID_80569 Human_SNP_ID_655652313 m1A Human chr19 + 2096218 2096218 2096218 CCGCCTCTGCCGCCCGCCTTCGCCCCTCCCGGACACCCACCTGATCGCCTCTGCCGCCCGCCTTC CCGCCTCTGCCGCCCGCCTTCGCCCCTCCCGGGCACCCACCTGATCGCCTCTGCCGCCCGCCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2096052..2096303 26863196 MeRIP-seq:(Medium) rs1399072876 Functional Loss SNV dbSNP153 33..33 33 - - - 80570 RMVar_ID_80570 Human_SNP_ID_655652480 m1A Human chr19 + 2096651 2096632 2096651 CCGGCCGAGGAGCGGGCACCGGCCATTGGCACAGGCACGGGCCATTGGCGCATGCGTAGGGCGCG CCGGCCGAGGAGCG___________________GGCACGGGCCATTGGCGCATGCGTAGGGCGCG GGGCACCGGCCATTGGCACA G IZUMO4 Ensembl:ENSG00000099840 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2096626..2096874 26863196 MeRIP-seq:(Medium) rs1313632606 Functional Loss DEL dbSNP153 15..33 33 - - - 80571 RMVar_ID_80571 Human_SNP_ID_655652490 m1A Human chr19 + 2096651 2096651 2096651 CCGGCCGAGGAGCGGGCACCGGCCATTGGCACAGGCACGGGCCATTGGCGCATGCGTAGGGCGCG CCGGCCGAGGAGCGGGCACCGGCCATTGGCACGGGCACGGGCCATTGGCGCATGCGTAGGGCGCG A G IZUMO4 Ensembl:ENSG00000099840 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2096626..2096874 26863196 MeRIP-seq:(Medium) rs1459716744 Functional Loss SNV dbSNP153 33..33 33 - - - 80572 RMVar_ID_80572 Human_SNP_ID_655657400 m1A Human chr19 - 2108688 2108687 2108688 CCAGGGCCACCATGTCTGCCTCCTGGTGAAAAAGGTGAGCCTCGGGCTGCTGTGCACACCCTGGC CCAGGGCCACCATGTCTGCCTCCTGGTGAAAA_GGTGAGCCTCGGGCTGCTGTGCACACCCTGGC CT C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1167169768 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1934890,Human_Splice_Rec_1934891,Human_Splice_Rec_1934948,Human_Splice_Rec_1934949,Human_Splice_Rec_1934958,Human_Splice_Rec_1934959,Human_Splice_Rec_1934966,Human_Splice_Rec_1934967,Human_Splice_Rec_1935012,Human_Splice_Rec_1935013,Human_Splice_Rec_1935024,Human_Splice_Rec_1935025,Human_Splice_Rec_1935036,Human_Splice_Rec_1935037,Human_Splice_Rec_1935047 RMVar_hsa_circ_24503,RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146 80573 RMVar_ID_80573 Human_SNP_ID_655657405 m1A Human chr19 + 2108708 2108708 2108708 CCGAGGCTCACCTTTTTCACCAGGAGGCAGACATGGTGGCCCTGGATGGAGCGGCTGTACATGGA CCGAGGCTCACCTTTTTCACCAGGAGGCAGACGTGGTGGCCCTGGATGGAGCGGCTGTACATGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:2108701..2108750 32194978 MeRIP-seq:(Medium) rs1365243095 Functional Loss SNV dbSNP153 33..33 33 - - - 80574 RMVar_ID_80574 Human_SNP_ID_655658663 m1A Human chr19 - 2111804 2111801 2111804 TGCTCCAGAAATCTCCCAAGCCTAAGAAGAAGAAGCACAGGAAGGAGAAGGAGGAGCGGACCAAA TGCTCCAGAAATCTCCCAAGCCTAAGAAGAAG___CACAGGAAGGAGAAGGAGGAGCGGACCAAA GCTT G AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:2111644..2111850;chr19:2111676..2111863 26863196 MeRIP-seq:(Medium) rs1422403091 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_52665,Human_RBP_ID_910084,Human_RBP_ID_1881530,Human_RBP_ID_9379997,Human_RBP_ID_22592921,Human_RBP_ID_22968015,Human_RBP_ID_24545379,Human_RBP_ID_25391041,Human_RBP_ID_26335085,Human_RBP_ID_27814878 Human_Splice_Rec_1934878,Human_Splice_Rec_1934936,Human_Splice_Rec_1935000,Human_Splice_Rec_1935052 RMVar_hsa_circ_24503,RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_61263,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_265929,RMVar_hsa_circ_191152 80575 RMVar_ID_80575 Human_SNP_ID_655658664 m1A Human chr19 - 2111804 2111804 2111804 TGCTCCAGAAATCTCCCAAGCCTAAGAAGAAGAAGCACAGGAAGGAGAAGGAGGAGCGGACCAAA TGCTCCAGAAATCTCCCAAGCCTAAGAAGAAGCAGCACAGGAAGGAGAAGGAGGAGCGGACCAAA T G AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:2111644..2111850;chr19:2111676..2111863 26863196 MeRIP-seq:(Medium) rs201127154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52665,Human_RBP_ID_910084,Human_RBP_ID_1881530,Human_RBP_ID_9379997,Human_RBP_ID_22592921,Human_RBP_ID_22968015,Human_RBP_ID_24545379,Human_RBP_ID_25391041,Human_RBP_ID_26335085,Human_RBP_ID_27814878 Human_Splice_Rec_1934878,Human_Splice_Rec_1934936,Human_Splice_Rec_1935000,Human_Splice_Rec_1935052 RMVar_hsa_circ_24503,RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_61263,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_265929,RMVar_hsa_circ_191152 80576 RMVar_ID_80576 Human_SNP_ID_655658669 m1A Human chr19 + 2111814 2111814 2111814 TCCTCCTTCTCCTTCCTGTGCTTCTTCTTCTTAGGCTTGGGAGATTTCTGGAGCAAGAGGAGGGT TCCTCCTTCTCCTTCCTGTGCTTCTTCTTCTTCGGCTTGGGAGATTTCTGGAGCAAGAGGAGGGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2111676..2111870 26863196 MeRIP-seq:(Medium) rs779370812 Functional Loss SNV dbSNP153 33..33 33 - - - 80577 RMVar_ID_80577 Human_SNP_ID_655659039 m1A Human chr19 - 2112812 2112812 2112812 CCCCAGGGGCTGTGGAGGGCTGCATGAGCCCCAGCACCCCAACGTGGGGCCGGACACAGCTTCCG CCCCAGGGGCTGTGGAGGGCTGCATGAGCCCCGGCACCCCAACGTGGGGCCGGACACAGCTTCCG T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2112809..2112950 26863196 MeRIP-seq:(Medium) rs1271670472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_61263,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_265929,RMVar_hsa_circ_191152 80578 RMVar_ID_80578 Human_SNP_ID_655659595 m1A Human chr19 - 2114210 2114210 2114210 ATCCCCTGAGAAGGACGTTCCCATGGTAGAAAAGAAGAGCAAGAAACCCAAGAAGAAAGAGAAAA ATCCCCTGAGAAGGACGTTCCCATGGTAGAAAGGAAGAGCAAGAAACCCAAGAAGAAAGAGAAAA T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:2114126..2114325;chr19:2114093..2114325 26863196 MeRIP-seq:(Medium) rs772475503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52669,Human_RBP_ID_1575246,Human_RBP_ID_13407214,Human_RBP_ID_17498334,Human_RBP_ID_18412409,Human_RBP_ID_18440842,Human_RBP_ID_24545382,Human_RBP_ID_26336962 Human_Splice_Rec_1934876,Human_Splice_Rec_1934877,Human_Splice_Rec_1934930,Human_Splice_Rec_1934931,Human_Splice_Rec_1934994,Human_Splice_Rec_1934995,Human_Splice_Rec_1935049 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_61263,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_117089,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_191153 80579 RMVar_ID_80579 Human_SNP_ID_655659613 m1A Human chr19 + 2114241 2114241 2114241 CTTTTCTACCATGGGAACGTCCTTCTCAGGGGATTTTGAGGTCTCGGTGTTTCTGTGTTTCTGAA CTTTTCTACCATGGGAACGTCCTTCTCAGGGGGTTTTGAGGTCTCGGTGTTTCTGTGTTTCTGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2114126..2114330 26863196 MeRIP-seq:(Medium) rs756070003 Functional Loss SNV dbSNP153 33..33 33 - - - 80580 RMVar_ID_80580 Human_SNP_ID_655660049 m1A Human chr19 - 2115319 2115314 2115320 GGACAAGAGGAGGAAAAAGAGGAAGGAGAAGGAGAAGAAGGGCAAGCGCCGCCACAGCTCGCTGC GGACAAGAGGAGGAAAAAGAGGAAGGAGAAG______AAGGGCAAGCGCCGCCACAGCTCGCTGC TCTTCTC T AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2115269..2115625 26863196 MeRIP-seq:(Medium) rs769722214 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_52673,Human_RBP_ID_3954059,Human_RBP_ID_4513254,Human_RBP_ID_8838904,Human_RBP_ID_9294038,Human_RBP_ID_9380002,Human_RBP_ID_22533265,Human_RBP_ID_22977964,Human_RBP_ID_24552749,Human_RBP_ID_26335094,Human_RBP_ID_27814880 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_117089,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_191153,RMVar_hsa_circ_79906,RMVar_hsa_circ_191155 80581 RMVar_ID_80581 Human_SNP_ID_655660051 m1A Human chr19 - 2115319 2115317 2115320 GGACAAGAGGAGGAAAAAGAGGAAGGAGAAGGAGAAGAAGGGCAAGCGCCGCCACAGCTCGCTGC GGACAAGAGGAGGAAAAAGAGGAAGGAGAAG___AAGAAGGGCAAGCGCCGCCACAGCTCGCTGC TCTC T AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2115269..2115625 26863196 MeRIP-seq:(Medium) rs992362360 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_52673,Human_RBP_ID_3954059,Human_RBP_ID_4513254,Human_RBP_ID_8838904,Human_RBP_ID_9294038,Human_RBP_ID_9380002,Human_RBP_ID_22533265,Human_RBP_ID_22977964,Human_RBP_ID_24552749,Human_RBP_ID_26335094,Human_RBP_ID_27814880 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_117089,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_191153,RMVar_hsa_circ_79906,RMVar_hsa_circ_191155 80582 RMVar_ID_80582 Human_SNP_ID_655660064 m1A Human chr19 - 2115336 2115336 2115336 CGGCAGAAGCTGGAGAAGGACAAGAGGAGGAAAAAGAGGAAGGAGAAGGAGAAGAAGGGCAAGCG CGGCAGAAGCTGGAGAAGGACAAGAGGAGGAAGAAGAGGAAGGAGAAGGAGAAGAAGGGCAAGCG T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2115238..2115550 26863196 MeRIP-seq:(Medium) rs1001166673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52673,Human_RBP_ID_8233558,Human_RBP_ID_26335094,Human_RBP_ID_27815767 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_117089,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_191153,RMVar_hsa_circ_79906,RMVar_hsa_circ_191155 80583 RMVar_ID_80583 Human_SNP_ID_655660070 m1A Human chr19 - 2115352 2115350 2115353 GGAGGAGCGGCGGCACCGGCAGAAGCTGGAGAAGGACAAGAGGAGGAAAAAGAGGAAGGAGAAGG GGAGGAGCGGCGGCACCGGCAGAAGCTGGAG___GACAAGAGGAGGAAAAAGAGGAAGGAGAAGG CCTT C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2115183..2115645 26863196 MeRIP-seq:(Medium) rs1401450864 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_52673,Human_RBP_ID_8233558,Human_RBP_ID_9293176,Human_RBP_ID_22810073,Human_RBP_ID_26335095 Human_miRNA_ID_2255621,Human_miRNA_ID_2255622 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_117089,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_191153,RMVar_hsa_circ_79906,RMVar_hsa_circ_191155 80584 RMVar_ID_80584 Human_SNP_ID_655662149 m1A Human chr19 + 2120898 2120898 2120898 AGAACTCCCCGCAGATCCAGGCGGCAGCGTACAGCACCTCACAGATCCCGTTCCGCTGGGTGCTG AGAACTCCCCGCAGATCCAGGCGGCAGCGTACGGCACCTCACAGATCCCGTTCCGCTGGGTGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2117201..2120925 32194978 MeRIP-seq:(Medium) rs777204449 Functional Loss SNV dbSNP153 33..33 33 - - - 80585 RMVar_ID_80585 Human_SNP_ID_655662221 m1A Human chr19 - 2121052 2121052 2121052 GCATCCTGGTGGAGCTGACCCGGCTGGAGGGCACACGGCACGGCCACCTCATCGCCGCCCAAATG GCATCCTGGTGGAGCTGACCCGGCTGGAGGGCGCACGGCACGGCCACCTCATCGCCGCCCAAATG T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2121001..2121075 32194978 MeRIP-seq:(Medium) rs755109870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912904,Human_RBP_ID_9380011,Human_RBP_ID_18191689,Human_RBP_ID_18995862 Human_Splice_Rec_1934862,Human_Splice_Rec_1934916,Human_Splice_Rec_1934980,Human_Splice_Rec_1935088,Human_Splice_Rec_1935102 RMVar_hsa_circ_5689,RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_64131,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_124947,RMVar_hsa_circ_108494,RMVar_hsa_circ_84167,RMVar_hsa_circ_106942,RMVar_hsa_circ_191156,RMVar_hsa_circ_191157,RMVar_hsa_circ_85326,RMVar_hsa_circ_191158,RMVar_hsa_circ_191162,RMVar_hsa_circ_191159,RMVar_hsa_circ_191160,RMVar_hsa_circ_101419,RMVar_hsa_circ_371092,RMVar_hsa_circ_78986,RMVar_hsa_circ_191161,RMVar_hsa_circ_52156,RMVar_hsa_circ_191163 80586 RMVar_ID_80586 Human_SNP_ID_655664908 m1A Human chr19 + 2128482 2128442 2128482 CCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGACACTGCACCCCGTGGAGCCGGCCCGCCCCACA _________________________________CACTGCACCCCGTGGAGCCGGCCCGCCCCACA GCACTGCACCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2128471..2128589 26863196 MeRIP-seq:(Medium) rs1180928054 Functional Loss DEL dbSNP153 1..33 33 - - - 80587 RMVar_ID_80587 Human_SNP_ID_655664962 m1A Human chr19 + 2128482 2128482 2128482 CCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGACACTGCACCCCGTGGAGCCGGCCCGCCCCACA CCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGCCACTGCACCCCGTGGAGCCGGCCCGCCCCACA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2128471..2128589 26863196 MeRIP-seq:(Medium) rs950490596 Functional Loss SNV dbSNP153 33..33 33 - - - 80588 RMVar_ID_80588 Human_SNP_ID_655664963 m1A Human chr19 + 2128482 2128482 2128482 CCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGACACTGCACCCCGTGGAGCCGGCCCGCCCCACA CCCCGTGGAGCCGGCCCGCCCCCGCCGCTCCGGCACTGCACCCCGTGGAGCCGGCCCGCCCCACA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2128471..2128589 26863196 MeRIP-seq:(Medium) rs950490596 Functional Loss SNV dbSNP153 33..33 33 - - - 80589 RMVar_ID_80589 Human_SNP_ID_655665301 m1A Human chr19 - 2129141 2129141 2129141 GTCCCCACAGTTCGGTGCTCTTACTCCTTTGGAACCGCGGCTGGGCAAGAAGCTGATCGAGCCCC GTCCCCACAGTTCGGTGCTCTTACTCCTTTGGGACCGCGGCTGGGCAAGAAGCTGATCGAGCCCC T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2129051..2129400 26863196 MeRIP-seq:(Medium) rs17850613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8830860,Human_RBP_ID_13408504,Human_RBP_ID_17267285 Human_Splice_Rec_1934851,Human_Splice_Rec_1934905,Human_Splice_Rec_1934969,Human_Splice_Rec_1935077,Human_Splice_Rec_1935093 Human_miRNA_ID_2917550 RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_191152,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_124947,RMVar_hsa_circ_108494,RMVar_hsa_circ_106942,RMVar_hsa_circ_191156,RMVar_hsa_circ_191157,RMVar_hsa_circ_85326,RMVar_hsa_circ_191158,RMVar_hsa_circ_191162,RMVar_hsa_circ_191159,RMVar_hsa_circ_101419,RMVar_hsa_circ_371092,RMVar_hsa_circ_191161,RMVar_hsa_circ_37558,RMVar_hsa_circ_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_80395,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169,RMVar_hsa_circ_288151,RMVar_hsa_circ_370198,RMVar_hsa_circ_125650,RMVar_hsa_circ_191171,RMVar_hsa_circ_191173,RMVar_hsa_circ_17708,RMVar_hsa_circ_191172,RMVar_hsa_circ_376261,RMVar_hsa_circ_191170,RMVar_hsa_circ_344562,RMVar_hsa_circ_191174,RMVar_hsa_circ_191175 80590 RMVar_ID_80590 Human_SNP_ID_655667728 m1A Human chr19 - 2135883 2135883 2135883 GCGGGTTTTGCAGGTGGTAACTGGGAGGGAGGAGGGTGGAGGGCTCCAGCCGCCCTAGGTACCCA GCGGGTTTTGCAGGTGGTAACTGGGAGGGAGGGGGGTGGAGGGCTCCAGCCGCCCTAGGTACCCA T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2135881..2136007 26863196 MeRIP-seq:(Medium) rs1421082543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8034,Human_RBP_ID_52693,Human_RBP_ID_3580170,Human_RBP_ID_3954068,Human_RBP_ID_5130121,Human_RBP_ID_5191873,Human_RBP_ID_5319890,Human_RBP_ID_6730321,Human_RBP_ID_8099586,Human_RBP_ID_8195437,Human_RBP_ID_8233560,Human_RBP_ID_8942328,Human_RBP_ID_9329465,Human_RBP_ID_9425069,Human_RBP_ID_13409539,Human_RBP_ID_17568246,Human_RBP_ID_18489198,Human_RBP_ID_18944677,Human_RBP_ID_22371031,Human_RBP_ID_22476355,Human_RBP_ID_22545329,Human_RBP_ID_22720355,Human_RBP_ID_26784908 RMVar_hsa_circ_104689,RMVar_hsa_circ_114869,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_191154,RMVar_hsa_circ_109400,RMVar_hsa_circ_124947,RMVar_hsa_circ_191157,RMVar_hsa_circ_85326,RMVar_hsa_circ_191162,RMVar_hsa_circ_191159,RMVar_hsa_circ_371092,RMVar_hsa_circ_22337,RMVar_hsa_circ_37558,RMVar_hsa_circ_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_80395,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169,RMVar_hsa_circ_288151,RMVar_hsa_circ_191171,RMVar_hsa_circ_376261,RMVar_hsa_circ_191170,RMVar_hsa_circ_344562,RMVar_hsa_circ_103983,RMVar_hsa_circ_108352,RMVar_hsa_circ_191174,RMVar_hsa_circ_191175,RMVar_hsa_circ_191177,RMVar_hsa_circ_98902,RMVar_hsa_circ_191176,RMVar_hsa_circ_54191,RMVar_hsa_circ_94546,RMVar_hsa_circ_191178,RMVar_hsa_circ_191179,RMVar_hsa_circ_25659 80591 RMVar_ID_80591 Human_SNP_ID_655667734 m1A Human chr19 + 2135907 2135907 2135907 CTCCACCCTCCTCCCTCCCAGTTACCACCTGCAAAACCCGCCCCCATCCTCCTCTTAGCGGGCCA CTCCACCCTCCTCCCTCCCAGTTACCACCTGCTAAACCCGCCCCCATCCTCCTCTTAGCGGGCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2135903..2136039 26863196 MeRIP-seq:(Medium) rs895888810 Functional Loss SNV dbSNP153 33..33 33 - - - 80592 RMVar_ID_80592 Human_SNP_ID_655673134 m1A Human chr19 - 2151288 2151288 2151288 GGTGAAGGGCAGCATCGACCGCATGTTCGACAAGAATCTGCAGGACTTGGTCCGCGGCATCCGTA GGTGAAGGGCAGCATCGACCGCATGTTCGACAGGAATCTGCAGGACTTGGTCCGCGGCATCCGTA T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2151204..2151518 26863196 MeRIP-seq:(Medium) rs1190784050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52702,Human_RBP_ID_303444,Human_RBP_ID_1557298,Human_RBP_ID_1881798,Human_RBP_ID_4513490,Human_RBP_ID_8838913,Human_RBP_ID_9328198,Human_RBP_ID_9381596,Human_RBP_ID_13410595,Human_RBP_ID_18725579,Human_RBP_ID_27573062 Human_Splice_Rec_1934839,Human_Splice_Rec_1934893 RMVar_hsa_circ_103983,RMVar_hsa_circ_191179,RMVar_hsa_circ_191183,RMVar_hsa_circ_86711 80593 RMVar_ID_80593 Human_SNP_ID_655673215 m1A Human chr19 + 2151482 2151482 2151482 AAGCTCCCAGGCCAGGGCGGCGGCGGGGTCCAAGGACCGCGGCAGAGGCGGCGACCCGCTCGGCA AAGCTCCCAGGCCAGGGCGGCGGCGGGGTCCACGGACCGCGGCAGAGGCGGCGACCCGCTCGGCA A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2151443..2151531 26863410 MeRIP-seq:(Medium) rs1238124448 Functional Loss SNV dbSNP153 33..33 33 - - - 80594 RMVar_ID_80594 Human_SNP_ID_655677601 m1A Human chr19 - 2164086 2164079 2164086 GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCCTCGGCCTCG GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGG_______GGGGAGGGGGCCTGGCCTCGGCCTCG CTCAGCCT C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2163984..2164090 26863410 MeRIP-seq:(Medium) rs1360978542 Functional Loss DEL dbSNP153 33..39 33 - - - 80595 RMVar_ID_80595 Human_SNP_ID_655677605 m1A Human chr19 - 2164095 2164083 2164096 CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCC CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGG_____________CTGAGGGGAGGGGGCCTGGCC GCCTCCCGCCCCTC G AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2163971..2164140 26863196 MeRIP-seq:(Medium) rs1055259491 Functional Loss DEL dbSNP153 32..44 33 - - - 80596 RMVar_ID_80596 Human_SNP_ID_655677606 m1A Human chr19 - 2164086 2164085 2164086 GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCCTCGGCCTCG GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGG_GGCTGAGGGGAGGGGGCCTGGCCTCGGCCTCG CT C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2163984..2164090 26863410 MeRIP-seq:(Medium) rs1229982800 Functional Loss DEL dbSNP153 33..33 33 - - - 80597 RMVar_ID_80597 Human_SNP_ID_655677607 m1A Human chr19 - 2164086 2164086 2164086 GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCCTCGGCCTCG GCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGGGGCTGAGGGGAGGGGGCCTGGCCTCGGCCTCG T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2163984..2164090 26863410 MeRIP-seq:(Medium) rs923250616 Functional Loss SNV dbSNP153 33..33 33 - - - 80598 RMVar_ID_80598 Human_SNP_ID_655677614 m1A Human chr19 - 2164095 2164094 2164095 CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCC CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGGG_GGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCC CT C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2163971..2164140 26863196 MeRIP-seq:(Medium) rs1442491612 Functional Loss DEL dbSNP153 33..33 33 - - - 80599 RMVar_ID_80599 Human_SNP_ID_655677616 m1A Human chr19 - 2164095 2164095 2164095 CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGGGAGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCC CGCCGGTGGGCGGAGGAGGGCGGGCGGGAGGGGGGGGCGGGAGGCTGAGGGGAGGGGGCCTGGCC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2163971..2164140 26863196 MeRIP-seq:(Medium) rs989293530 Functional Loss SNV dbSNP153 33..33 33 - - - 80600 RMVar_ID_80600 Human_SNP_ID_655677683 m1A Human chr19 - 2164198 2164198 2164198 CAGCCCCCACGGGCGACTTCAGTCTCAGCTCCAGCTTCTCCCCCATGTCCGCGCGCGCGGCCGCC CAGCCCCCACGGGCGACTTCAGTCTCAGCTCCGGCTTCTCCCCCATGTCCGCGCGCGCGGCCGCC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2164148..2164249 32194978 MeRIP-seq:(Medium) rs954850357 Functional Loss SNV dbSNP153 33..33 33 - - - 80601 RMVar_ID_80601 Human_SNP_ID_655693674 m1A Human chr19 - 2210725 2210725 2210725 TTCATCTTCTTGGGGCGCCCGCGCTTGCGGCCAGCCATCTTCCTCCCCTTCTTGTTTAGCTTCTT TTCATCTTCTTGGGGCGCCCGCGCTTGCGGCCGGCCATCTTCCTCCCCTTCTTGTTTAGCTTCTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2210693..2210780 26863196 MeRIP-seq:(Medium) rs1285916870 Functional Loss SNV dbSNP153 33..33 33 - - - 80602 RMVar_ID_80602 Human_SNP_ID_655694090 m1A Human chr19 + 2211802 2211802 2211802 CCTGCAGTTCCTGGCATACACAAAGACCCCCCAGTACAAGGCCAGCCTGCAGGAGCTGCTGGGCC CCTGCAGTTCCTGGCATACACAAAGACCCCCCGGTACAAGGCCAGCCTGCAGGAGCTGCTGGGCC A G DOT1L Ensembl:ENSG00000104885 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2211720..2211832 26863196 MeRIP-seq:(Medium) rs767916803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907005,Human_RBP_ID_3954091,Human_RBP_ID_18994010,Human_RBP_ID_26335113 Human_Splice_Rec_1935144,Human_Splice_Rec_1935145 RMVar_hsa_circ_112069,RMVar_hsa_circ_268586,RMVar_hsa_circ_268349,RMVar_hsa_circ_119718,RMVar_hsa_circ_120678,RMVar_hsa_circ_113718,RMVar_hsa_circ_102769,RMVar_hsa_circ_109532,RMVar_hsa_circ_110095,RMVar_hsa_circ_101110,RMVar_hsa_circ_191188,RMVar_hsa_circ_191192,RMVar_hsa_circ_81673,RMVar_hsa_circ_191193,RMVar_hsa_circ_191190,RMVar_hsa_circ_191191,RMVar_hsa_circ_191189,RMVar_hsa_circ_41619,RMVar_hsa_circ_191186,RMVar_hsa_circ_191187,RMVar_hsa_circ_191185,RMVar_hsa_circ_126529,RMVar_hsa_circ_123413,RMVar_hsa_circ_45378,RMVar_hsa_circ_33741,RMVar_hsa_circ_115808,RMVar_hsa_circ_191207,RMVar_hsa_circ_191208,RMVar_hsa_circ_191206,RMVar_hsa_circ_127010,RMVar_hsa_circ_125544,RMVar_hsa_circ_115813,RMVar_hsa_circ_107867,RMVar_hsa_circ_85658,RMVar_hsa_circ_77176,RMVar_hsa_circ_111617,RMVar_hsa_circ_191219,RMVar_hsa_circ_191221,RMVar_hsa_circ_191222,RMVar_hsa_circ_191220,RMVar_hsa_circ_191217,RMVar_hsa_circ_191218,RMVar_hsa_circ_191216,RMVar_hsa_circ_45222,RMVar_hsa_circ_51545,RMVar_hsa_circ_191231,RMVar_hsa_circ_39463,RMVar_hsa_circ_27174,RMVar_hsa_circ_37252,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232 80603 RMVar_ID_80603 Human_SNP_ID_655698416 m1A Human chr19 + 2223332 2223332 2223332 CCCTGGAGATTACAGCCATCTCGTCCCCGGAGACCTCCCTGAAGAGCTCCCCTGTGCCCTACCAG CCCTGGAGATTACAGCCATCTCGTCCCCGGAGTCCTCCCTGAAGAGCTCCCCTGTGCCCTACCAG A T DOT1L Ensembl:ENSG00000104885 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:2223229..2223427;chr19:2223213..2223374 26863196 MeRIP-seq:(Medium) rs767505976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8830968,Human_RBP_ID_18191696,Human_RBP_ID_26335117,Human_RBP_ID_27466046 Human_Splice_Rec_1935162,Human_Splice_Rec_1935214 Human_miRNA_ID_2030502,Human_miRNA_ID_2690956,Human_miRNA_ID_2694269 RMVar_hsa_circ_268586,RMVar_hsa_circ_119718,RMVar_hsa_circ_109532,RMVar_hsa_circ_191186,RMVar_hsa_circ_191185,RMVar_hsa_circ_9493,RMVar_hsa_circ_115808,RMVar_hsa_circ_107867,RMVar_hsa_circ_191217,RMVar_hsa_circ_191216,RMVar_hsa_circ_51545,RMVar_hsa_circ_39463,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232,RMVar_hsa_circ_78107,RMVar_hsa_circ_191236,RMVar_hsa_circ_191237,RMVar_hsa_circ_113062 80604 RMVar_ID_80604 Human_SNP_ID_655699721 m1A Human chr19 - 2226578 2226578 2226578 GTCCGAGCCCTCCTTGCCGCGCTGCGAGGGGAAGCTCAGCGGGGAGCTCAGGCCGGCCGCCTCGG GTCCGAGCCCTCCTTGCCGCGCTGCGAGGGGAGGCTCAGCGGGGAGCTCAGGCCGGCCGCCTCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2226527..2227242 26863196 MeRIP-seq:(Medium) rs907579305 Functional Loss SNV dbSNP153 33..33 33 - - - 80605 RMVar_ID_80605 Human_SNP_ID_655699752 m1A Human chr19 + 2226626 2226626 2226626 GCAAGGAGGGCTCGGACGCCAACCCTTTCCTGAGCAAGAGGCAGCTGGACGGCCTGGCTGGGCTG GCAAGGAGGGCTCGGACGCCAACCCTTTCCTGTGCAAGAGGCAGCTGGACGGCCTGGCTGGGCTG A T DOT1L Ensembl:ENSG00000104885 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:2226576..2226875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22069429,Human_RBP_ID_27466051 RMVar_hsa_circ_268586,RMVar_hsa_circ_9493,RMVar_hsa_circ_107867,RMVar_hsa_circ_191216,RMVar_hsa_circ_39463,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232,RMVar_hsa_circ_78107,RMVar_hsa_circ_191236,RMVar_hsa_circ_191237,RMVar_hsa_circ_113062,RMVar_hsa_circ_100566,RMVar_hsa_circ_191238 80606 RMVar_ID_80606 Human_SNP_ID_655700722 m1A Human chr19 - 2228002 2228002 2228002 AGCAGCGTTGGGGGAGGAGGCAAGGCGGCGTTAGGTGGAGGGGGGGCGTGGAGGACGGGCGGCCC AGCAGCGTTGGGGGAGGAGGCAAGGCGGCGTTGGGTGGAGGGGGGGCGTGGAGGACGGGCGGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2227999..2228164 26863196 MeRIP-seq:(Medium) rs1159924137 Functional Loss SNV dbSNP153 33..33 33 - - - 80607 RMVar_ID_80607 Human_SNP_ID_655700751 m1A Human chr19 - 2228047 2228047 2228047 AGGGACGCGAGGCTCTGCAGAAGCGCGGGCTCAGGGTTAGAGGCCAGCAGCGTTGGGGGAGGAGG AGGGACGCGAGGCTCTGCAGAAGCGCGGGCTCGGGGTTAGAGGCCAGCAGCGTTGGGGGAGGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2228039..2228142 26863196 MeRIP-seq:(Medium) rs1472070806 Functional Loss SNV dbSNP153 33..33 33 - - - 80608 RMVar_ID_80608 Human_SNP_ID_655701060 m1A Human chr19 + 2228541 2228541 2228541 GGGAGACCAGGGAGATGGTCGCGAGAGGAGGGACTACAGGACGGGCACCAGCCATGGAGTGGCCT GGGAGACCAGGGAGATGGTCGCGAGAGGAGGGGCTACAGGACGGGCACCAGCCATGGAGTGGCCT A G DOT1L Ensembl:ENSG00000104885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2228447..2228556 26863196 MeRIP-seq:(Medium) rs893449102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263595,Human_RBP_ID_3580230,Human_RBP_ID_3955900,Human_RBP_ID_5088701,Human_RBP_ID_5144894,Human_RBP_ID_5650567,Human_RBP_ID_8099657,Human_RBP_ID_8195466,Human_RBP_ID_9341107,Human_RBP_ID_13412716,Human_RBP_ID_18412218,Human_RBP_ID_18944702,Human_RBP_ID_21930099,Human_RBP_ID_21978363,Human_RBP_ID_22416672,Human_RBP_ID_22661633,Human_RBP_ID_22741550,Human_RBP_ID_24375191,Human_RBP_ID_25441000,Human_RBP_ID_26335119,Human_RBP_ID_27839170 RMVar_hsa_circ_268586,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232,RMVar_hsa_circ_78107,RMVar_hsa_circ_191236,RMVar_hsa_circ_191237,RMVar_hsa_circ_113062,RMVar_hsa_circ_100566,RMVar_hsa_circ_191238 80609 RMVar_ID_80609 Human_SNP_ID_655701689 m1A Human chr19 + 2230209 2230209 2230209 GGCCCGCGCCTGCCTCCACCCGCTTGGTGCTGACTAGACGCTGACAACGCCGAACCCCGTTCTCG GGCCCGCGCCTGCCTCCACCCGCTTGGTGCTGCCTAGACGCTGACAACGCCGAACCCCGTTCTCG A C DOT1L Ensembl:ENSG00000104885 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2230159..2230357 26863196 MeRIP-seq:(Medium) rs1041849396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517688,Human_RBP_ID_1557457,Human_RBP_ID_13412735 RMVar_hsa_circ_268586,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232,RMVar_hsa_circ_78107,RMVar_hsa_circ_191236,RMVar_hsa_circ_191237,RMVar_hsa_circ_113062,RMVar_hsa_circ_100566,RMVar_hsa_circ_191238 80610 RMVar_ID_80610 Human_SNP_ID_655701732 m1A Human chr19 - 2230282 2230282 2230282 AGGAATGTGGTGGCGACGGGCCTGCCTTTGGTACGGGAGCAGCGCGTCGGGGGAGCCGGCCGGGC AGGAATGTGGTGGCGACGGGCCTGCCTTTGGTGCGGGAGCAGCGCGTCGGGGGAGCCGGCCGGGC T C PLEKHJ1 Ensembl:ENSG00000104886 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:2230201..2230391 26863196 MeRIP-seq:(Medium) rs1397887430 Functional Loss SNV dbSNP153 33..33 33 - - - 80611 RMVar_ID_80611 Human_SNP_ID_655703094 m1A Human chr19 - 2233814 2233814 2233814 GGCGTGAGCGCAGGGCACGGTGGTCAGCGTGCAGCGGGACGGGACTGGCCCTGCCCAGCCATGAA GGCGTGAGCGCAGGGCACGGTGGTCAGCGTGCCGCGGGACGGGACTGGCCCTGCCCAGCCATGAA T G PLEKHJ1 Ensembl:ENSG00000104886 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2233651..2234292 26863196 MeRIP-seq:(Medium) rs1319082434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17131551,Human_RBP_ID_17656521,Human_RBP_ID_17918291,Human_RBP_ID_26471669 Human_Splice_Rec_1935252,Human_Splice_Rec_1935262,Human_Splice_Rec_1935278,Human_Splice_Rec_1935288,Human_Splice_Rec_1935298,Human_Splice_Rec_1935306 Human_miRNA_ID_1967458 RMVar_hsa_circ_85084,RMVar_hsa_circ_104204,RMVar_hsa_circ_88425,RMVar_hsa_circ_191239,RMVar_hsa_circ_191241,RMVar_hsa_circ_81471,RMVar_hsa_circ_191242,RMVar_hsa_circ_191240 80612 RMVar_ID_80612 Human_SNP_ID_655703833 m1A Human chr19 - 2235637 2235637 2235637 CTGTGTCCCCAGCCTGGCGCCACCCTCCTCAAACACAAGAGTGCATTGTCCACGGGCAGCTCAAG CTGTGTCCCCAGCCTGGCGCCACCCTCCTCAATCACAAGAGTGCATTGTCCACGGGCAGCTCAAG T A PLEKHJ1 Ensembl:ENSG00000104886 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2235628..2235778 26863196 MeRIP-seq:(Medium) rs889996485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907022,Human_RBP_ID_17081545 RMVar_hsa_circ_85084,RMVar_hsa_circ_88425,RMVar_hsa_circ_191239,RMVar_hsa_circ_191240 80613 RMVar_ID_80613 Human_SNP_ID_655703902 m1A Human chr19 + 2235756 2235752 2235756 CTGCGGGAAGCGCCGCTGGCTTCCCTAGCCCCACTCACTGATGGAGAAGGTGCCGGGCTCTTCCC CTGCGGGAAGCGCCGCTGGCTTCCCTAGC____CTCACTGATGGAGAAGGTGCCGGGCTCTTCCC CCCCA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2235751..2236025 32194978 MeRIP-seq:(Medium) rs1421571770 Functional Loss DEL dbSNP153 30..33 33 - - - 80614 RMVar_ID_80614 Human_SNP_ID_655704173 m1A Human chr19 - 2236252 2236252 2236252 GAGGGCGCGGCCCGGGTTCCCGTTCCCCGCGGAGCCATGCGGTACAACGAGAAGGAGCTGCAGGC GAGGGCGCGGCCCGGGTTCCCGTTCCCCGCGGGGCCATGCGGTACAACGAGAAGGAGCTGCAGGC T C PLEKHJ1 Ensembl:ENSG00000104886 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2235650..2236325;chr19:2235623..2236325;chr19:2235628..2236300 26863196 MeRIP-seq:(Medium) rs1419962147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517753,Human_RBP_ID_4557059,Human_RBP_ID_5116534,Human_RBP_ID_5469531,Human_RBP_ID_8942332,Human_RBP_ID_22977569 Human_Splice_Rec_1935227,Human_Splice_Rec_1935237,Human_Splice_Rec_1935245,Human_Splice_Rec_1935253,Human_Splice_Rec_1935263,Human_Splice_Rec_1935269,Human_Splice_Rec_1935293,Human_Splice_Rec_1935313 80615 RMVar_ID_80615 Human_SNP_ID_655704779 m1A Human chr19 + 2237795 2237795 2237795 GGCTTCAACATCATGCCAAAGGCGACCAGAACACGTTAGCTGGCCCCATTTTGCAGGTGCACCCC GGCTTCAACATCATGCCAAAGGCGACCAGAACCCGTTAGCTGGCCCCATTTTGCAGGTGCACCCC A C SF3A2 Ensembl:ENSG00000104897 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2237793..2244678 32194978 MeRIP-seq:(Medium) rs1007993354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1935361 80616 RMVar_ID_80616 Human_SNP_ID_655706480 m1A Human chr19 - 2243364 2243364 2243364 CAGACTGGGAGACACCTGTGGAGGCCAAGAGGAGAGTGAGGAAGATGGCTCAGAACTCGGGGCTG CAGACTGGGAGACACCTGTGGAGGCCAAGAGGCGAGTGAGGAAGATGGCTCAGAACTCGGGGCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2243361..2243575 26863196 MeRIP-seq:(Medium) rs1356929191 Functional Loss SNV dbSNP153 33..33 33 - - - 80617 RMVar_ID_80617 Human_SNP_ID_655706848 m1A Human chr19 - 2244644 2244644 2244644 TCCCCCTGACGTCAGCCACTCAGCCCGCCGCGAGCCGCCCGGAGCCAGGCAGAGGCCGCACCTCA TCCCCCTGACGTCAGCCACTCAGCCCGCCGCGGGCCGCCCGGAGCCAGGCAGAGGCCGCACCTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2244634..2244721 26863196 MeRIP-seq:(Medium) rs569729809 Functional Loss SNV dbSNP153 33..33 33 - - - 80618 RMVar_ID_80618 Human_SNP_ID_655707106 m1A Human chr19 - 2245430 2245427 2245431 TGGCTGCTCGCCGGGCCCTGCGGACAGGATGGAGGTGCTGCTGGGACCCCTCCACACACAGGCAC TGGCTGCTCGCCGGGCCCTGCGGACAGGATG____TGCTGCTGGGACCCCTCCACACACAGGCAC ACCTC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2245426..2245625 26863196 MeRIP-seq:(Medium) rs1198505215 Functional Loss DEL dbSNP153 32..35 33 - - - 80619 RMVar_ID_80619 Human_SNP_ID_655707137 m1A Human chr19 - 2245527 2245527 2245527 TCACCTTTGTAGCCCGGGCGGCCGATCTTCACAAACTTCTTCACCTCCACCTTGACCTTCTCAGG TCACCTTTGTAGCCCGGGCGGCCGATCTTCACGAACTTCTTCACCTCCACCTTGACCTTCTCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2245476..2245732 32194978 MeRIP-seq:(Medium) rs1209440456 Functional Loss SNV dbSNP153 33..33 33 - - - 80620 RMVar_ID_80620 Human_SNP_ID_655707585 m1A Human chr19 + 2246943 2246943 2246943 CATGCCACGTCACCGCTTCATGTCTGCGTACGAGCAGAGGATCGAGCCTCCGGACCGGCGCTGGC CATGCCACGTCACCGCTTCATGTCTGCGTACGGGCAGAGGATCGAGCCTCCGGACCGGCGCTGGC A G SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2246813..2246977 26863196 MeRIP-seq:(Medium) rs202183201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241243,Human_RBP_ID_4564765,Human_RBP_ID_8255885,Human_RBP_ID_8481255,Human_RBP_ID_18191703,Human_RBP_ID_18725800,Human_RBP_ID_18995920 Human_Splice_Rec_1935328,Human_Splice_Rec_1935329,Human_Splice_Rec_1935357 80621 RMVar_ID_80621 Human_SNP_ID_655707861 m1A Human chr19 - 2247578 2247577 2247578 ATCTCTCTGCTCGGCACCTGGGAGGGCGGGGGACAGAGAGGGCTCCTGGTCCCTGTGACCTCAGG ATCTCTCTGCTCGGCACCTGGGAGGGCGGGGG_CAGAGAGGGCTCCTGGTCCCTGTGACCTCAGG GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2247576..2247625 26863196 MeRIP-seq:(Medium) rs759626218 Functional Loss DEL dbSNP153 33..33 33 - - - 80622 RMVar_ID_80622 Human_SNP_ID_655708035 m1A Human chr19 - 2247927 2247927 2247927 CAGGCCCTGTGGGGGGCATGGGTGGCAGAGGCAGGCCTCCTGGCGGGGGCGGTGGCAAAGACTCA CAGGCCCTGTGGGGGGCATGGGTGGCAGAGGCGGGCCTCCTGGCGGGGGCGGTGGCAAAGACTCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:2247801..2248598 26863410 MeRIP-seq:(Medium) rs770040121 Functional Loss SNV dbSNP153 33..33 33 - - - 80623 RMVar_ID_80623 Human_SNP_ID_655708062 m1A Human chr19 + 2247991 2247991 2247991 GCGCCCTCAGGGCCCCCGGGACCACCCCAGCTACCCCCGCCAGCTCCAGGGGTCCACCCCCCGGC GCGCCCTCAGGGCCCCCGGGACCACCCCAGCTCCCCCCGCCAGCTCCAGGGGTCCACCCCCCGGC A C SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:2247892..2248582 26863410 MeRIP-seq:(Medium) rs769950502 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_241246,Human_RBP_ID_517768,Human_RBP_ID_5130144 80624 RMVar_ID_80624 Human_SNP_ID_655708218 m1A Human chr19 + 2248198 2248177 2248198 CCAGCCCCCGGGGTTCACCCACCAGCCCCCGGAGTCCACCCACCAGCCCCTGGGGTTCACCCACC CCAGCCCCCGGG_____________________GTCCACCCACCAGCCCCTGGGGTTCACCCACC GGTTCACCCACCAGCCCCCGGA G SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2247576..2248675 26863196 MeRIP-seq:(Medium) rs763083610 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_5130146,Human_RBP_ID_5321036,Human_RBP_ID_17081547,Human_RBP_ID_17386548,Human_RBP_ID_18946213,Human_RBP_ID_21908692,Human_RBP_ID_22968132 Human_miRNA_ID_131967 80625 RMVar_ID_80625 Human_SNP_ID_655708221 m1A Human chr19 - 2248200 2248180 2248201 CTGGTGGGTGAACCCCAGGGGCTGGTGGGTGGACTCCGGGGGCTGGTGGGTGAACCCCGGGGGCT CTGGTGGGTGAACCCCAGGGGCTGGTGGGTG_____________________AACCCCGGGGGCT TCACCCACCAGCCCCCGGAGTC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2247801..2248650 26863196 MeRIP-seq:(Medium) rs764436602 Functional Loss DEL dbSNP153 32..52 33 - - - 80626 RMVar_ID_80626 Human_SNP_ID_655708234 m1A Human chr19 + 2248198 2248198 2248198 CCAGCCCCCGGGGTTCACCCACCAGCCCCCGGAGTCCACCCACCAGCCCCTGGGGTTCACCCACC CCAGCCCCCGGGGTTCACCCACCAGCCCCCGGGGTCCACCCACCAGCCCCTGGGGTTCACCCACC A G SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2247576..2248675 26863196 MeRIP-seq:(Medium) rs1321919075 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5130146,Human_RBP_ID_5321036,Human_RBP_ID_17081547,Human_RBP_ID_17386548,Human_RBP_ID_18946213,Human_RBP_ID_21908692,Human_RBP_ID_22968132 Human_miRNA_ID_131967 80627 RMVar_ID_80627 Human_SNP_ID_655708317 m1A Human chr19 + 2248324 2248324 2248324 CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCAGGGGTGCACCCACCAGCCCCAGGGATGCACCC CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCCGGGGTGCACCCACCAGCCCCAGGGATGCACCC A C SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1223953680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116535,Human_RBP_ID_5130147,Human_RBP_ID_5319914,Human_RBP_ID_8481260,Human_RBP_ID_17081548,Human_RBP_ID_17656526,Human_RBP_ID_18725811,Human_RBP_ID_18946213,Human_RBP_ID_22502045 80628 RMVar_ID_80628 Human_SNP_ID_655708318 m1A Human chr19 + 2248324 2248324 2248324 CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCAGGGGTGCACCCACCAGCCCCAGGGATGCACCC CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCGGGGGTGCACCCACCAGCCCCAGGGATGCACCC A G SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1223953680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116535,Human_RBP_ID_5130147,Human_RBP_ID_5319914,Human_RBP_ID_8481260,Human_RBP_ID_17081548,Human_RBP_ID_17656526,Human_RBP_ID_18725811,Human_RBP_ID_18946213,Human_RBP_ID_22502045 80629 RMVar_ID_80629 Human_SNP_ID_655708319 m1A Human chr19 + 2248324 2248324 2248324 CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCAGGGGTGCACCCACCAGCCCCAGGGATGCACCC CCAGCAGCCCCCGCCGTTCACCCTCAGGCCCCTGGGGTGCACCCACCAGCCCCAGGGATGCACCC A T SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5116535,Human_RBP_ID_5130147,Human_RBP_ID_5319914,Human_RBP_ID_8481260,Human_RBP_ID_17081548,Human_RBP_ID_17656526,Human_RBP_ID_18725811,Human_RBP_ID_18946213,Human_RBP_ID_22502045 80630 RMVar_ID_80630 Human_SNP_ID_655708351 m1A Human chr19 + 2248380 2248380 2248380 GATGCACCCTCAGGCCCCGGGGGTCCACCCCCAACCTCCCGGGGTCCATCCGTCGGCTCCTGGGG GATGCACCCTCAGGCCCCGGGGGTCCACCCCCCACCTCCCGGGGTCCATCCGTCGGCTCCTGGGG A C SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2247872..2248593 26863196 MeRIP-seq:(Medium) rs1233180288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240956,Human_RBP_ID_517776,Human_RBP_ID_1372333,Human_RBP_ID_1557543,Human_RBP_ID_5130148,Human_RBP_ID_5319915,Human_RBP_ID_17081548,Human_RBP_ID_18165912,Human_RBP_ID_18946214 80631 RMVar_ID_80631 Human_SNP_ID_655708352 m1A Human chr19 + 2248380 2248380 2248380 GATGCACCCTCAGGCCCCGGGGGTCCACCCCCAACCTCCCGGGGTCCATCCGTCGGCTCCTGGGG GATGCACCCTCAGGCCCCGGGGGTCCACCCCCGACCTCCCGGGGTCCATCCGTCGGCTCCTGGGG A G SF3A2 Ensembl:ENSG00000104897 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2247872..2248593 26863196 MeRIP-seq:(Medium) rs1233180288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240956,Human_RBP_ID_517776,Human_RBP_ID_1372333,Human_RBP_ID_1557543,Human_RBP_ID_5130148,Human_RBP_ID_5319915,Human_RBP_ID_17081548,Human_RBP_ID_18165912,Human_RBP_ID_18946214 80632 RMVar_ID_80632 Human_SNP_ID_655708408 m1A Human chr19 - 2248525 2248476 2248525 GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGGGAGGTATGTTCCCTGGGCCTTCGGAGGGAAGTGG GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGGG_________________________________ CCCCAATGCTGAGGCCCCCACTTCCCTCCGAAGGCCCAGGGAACATACCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:2248224..2248650;chr19:2248368..2248618 26863196 MeRIP-seq:(Medium) rs757857048 Functional Loss DEL dbSNP153 33..65 33 - - - 80633 RMVar_ID_80633 Human_SNP_ID_655708418 m1A Human chr19 - 2248525 2248496 2248525 GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGGGAGGTATGTTCCCTGGGCCTTCGGAGGGAAGTGG GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGGG_____________________________GTGG CTTCCCTCCGAAGGCCCAGGGAACATACCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:2248224..2248650;chr19:2248368..2248618 26863196 MeRIP-seq:(Medium) rs777413619 Functional Loss DEL dbSNP153 33..61 33 - - - 80634 RMVar_ID_80634 Human_SNP_ID_655708419 m1A Human chr19 - 2248525 2248497 2248526 GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGGGAGGTATGTTCCCTGGGCCTTCGGAGGGAAGTGG GGAGCAGCTTCTCAGTTGGTTGGGGGAGGGG_____________________________AGTGG TTCCCTCCGAAGGCCCAGGGAACATACCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:2248224..2248650;chr19:2248368..2248618 26863196 MeRIP-seq:(Medium) rs746687373 Functional Loss DEL dbSNP153 32..60 33 - - - 80635 RMVar_ID_80635 Human_SNP_ID_655709388 m1A Human chr19 - 2250445 2250445 2250445 GGGCACCCGGCAGCCCAGCCCTCGTCACAGTGACCTCAGGGCCAGGCCCAGGGTACAGCACCAGC GGGCACCCGGCAGCCCAGCCCTCGTCACAGTGGCCTCAGGGCCAGGCCCAGGGTACAGCACCAGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:2250303..2250552 26863410 MeRIP-seq:(Medium) rs1187172871 Functional Loss SNV dbSNP153 33..33 33 - - - 80636 RMVar_ID_80636 Human_SNP_ID_655709402 m1A Human chr19 + 2250478 2250470 2250478 CACTGTGACGAGGGCTGGGCTGCCGGGTGCCCAGGTACCAGGGAGTTGCATGGGGCAGTGCCCGG CACTGTGACGAGGGCTGGGCTGCCG________GGTACCAGGGAGTTGCATGGGGCAGTGCCCGG GGGTGCCCA G AMH Ensembl:ENSG00000104899 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2250467..2250672 26863196 MeRIP-seq:(Medium) rs1568393388 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_1557619,Human_RBP_ID_5321041,Human_RBP_ID_8481315,Human_RBP_ID_22070691,Human_RBP_ID_26783517 Human_Splice_Rec_1935379 80637 RMVar_ID_80637 Human_SNP_ID_655709414 m1A Human chr19 + 2250489 2250489 2250489 GGGCTGGGCTGCCGGGTGCCCAGGTACCAGGGAGTTGCATGGGGCAGTGCCCGGGCCGTGGCGGG GGGCTGGGCTGCCGGGTGCCCAGGTACCAGGGGGTTGCATGGGGCAGTGCCCGGGCCGTGGCGGG A G AMH Ensembl:ENSG00000104899 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2250439..2250658 26863196 MeRIP-seq:(Medium) rs775588008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909123,Human_RBP_ID_4514000,Human_RBP_ID_8481315,Human_RBP_ID_18166263,Human_RBP_ID_21978368,Human_RBP_ID_22070691,Human_RBP_ID_22477369,Human_RBP_ID_22810163,Human_RBP_ID_22978607,Human_RBP_ID_26335128,Human_RBP_ID_26783517 80638 RMVar_ID_80638 Human_SNP_ID_655709416 m1A Human chr19 - 2250491 2250491 2250491 CCCCCGCCACGGCCCGGGCACTGCCCCATGCAACTCCCTGGTACCTGGGCACCCGGCAGCCCAGC CCCCCGCCACGGCCCGGGCACTGCCCCATGCAGCTCCCTGGTACCTGGGCACCCGGCAGCCCAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2250442..2250575 26863196 MeRIP-seq:(Medium) rs764611221 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 80639 RMVar_ID_80639 Human_SNP_ID_655710397 m1A Human chr19 - 2251955 2251955 2251955 CTCGGGGCAGGAGTCCGCGCGGCGCAGGGGTCACCGGCAGCCACACTCGGTGGCCACCATGTTGG CTCGGGGCAGGAGTCCGCGCGGCGCAGGGGTCTCCGGCAGCCACACTCGGTGGCCACCATGTTGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr19:2251909..2252016;chr19:2250938..2251974 26863196,32194978 MeRIP-seq:(Medium) rs1407146845 Functional Loss SNV dbSNP153 33..33 33 - - - 80640 RMVar_ID_80640 Human_SNP_ID_655710398 m1A Human chr19 - 2251955 2251955 2251955 CTCGGGGCAGGAGTCCGCGCGGCGCAGGGGTCACCGGCAGCCACACTCGGTGGCCACCATGTTGG CTCGGGGCAGGAGTCCGCGCGGCGCAGGGGTCGCCGGCAGCCACACTCGGTGGCCACCATGTTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr19:2251909..2252016;chr19:2250938..2251974 26863196,32194978 MeRIP-seq:(Medium) rs1407146845 Functional Loss SNV dbSNP153 33..33 33 - - - 80641 RMVar_ID_80641 Human_SNP_ID_655716256 m1A Human chr19 - 2269576 2269576 2269576 ATTTCACCATCCGGCCGCTGGGGTCCGAAACCAGGAAAACCTCCGCTGCGTCTCTCCGCGCCGCC ATTTCACCATCCGGCCGCTGGGGTCCGAAACCGGGAAAACCTCCGCTGCGTCTCTCCGCGCCGCC T C JSRP1 Ensembl:ENSG00000167476 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:2269526..2269833 26863196 MeRIP-seq:(Medium) rs1463816604 Functional Loss SNV dbSNP153 33..33 33 - - - 80642 RMVar_ID_80642 Human_SNP_ID_655717194 m1A Human chr19 + 2271402 2271402 2271402 CTGCATCATCTTCAGTTCCAGGGTCTCCCTCCACTGCTGTAGTAACCCGGGTCCGGGGCCTCGGT CTGCATCATCTTCAGTTCCAGGGTCTCCCTCCGCTGCTGTAGTAACCCGGGTCCGGGGCCTCGGT A G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:2271376..2271425 26863196 MeRIP-seq:(Medium) rs761032839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55051,Human_RBP_ID_517820,Human_RBP_ID_914167,Human_RBP_ID_1372342,Human_RBP_ID_1557671,Human_RBP_ID_3565762,Human_RBP_ID_4564800,Human_RBP_ID_5499200,Human_RBP_ID_6732064,Human_RBP_ID_8481352,Human_RBP_ID_8831009,Human_RBP_ID_9291549,Human_RBP_ID_9328247,Human_RBP_ID_13413267,Human_RBP_ID_17267389,Human_RBP_ID_17498428,Human_RBP_ID_17655766,Human_RBP_ID_17918332,Human_RBP_ID_18191716,Human_RBP_ID_18461054,Human_RBP_ID_18725932,Human_RBP_ID_22446307,Human_RBP_ID_23175372,Human_RBP_ID_26474680,Human_RBP_ID_27271411,Human_RBP_ID_27466113 Human_Splice_Rec_1935418,Human_Splice_Rec_1935422,Human_Splice_Rec_1935428,Human_Splice_Rec_1935436,Human_Splice_Rec_1935444,Human_Splice_Rec_1935448 RMVar_hsa_circ_123026,RMVar_hsa_circ_332875,RMVar_hsa_circ_317653,RMVar_hsa_circ_191247,RMVar_hsa_circ_191248 80643 RMVar_ID_80643 Human_SNP_ID_655717583 m1A Human chr19 + 2272055 2272055 2272055 GCGGGGAGTGCTCACCCAGGGGAGCAGGGACCAGGTGCGGGTTGCTGCCCAAGGGGTGCAGGGAC GCGGGGAGTGCTCACCCAGGGGAGCAGGGACCGGGTGCGGGTTGCTGCCCAAGGGGTGCAGGGAC A G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2271755..2272113 26863196 MeRIP-seq:(Medium) rs573116700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914171,Human_RBP_ID_1067160,Human_RBP_ID_5372739,Human_RBP_ID_6732073,Human_RBP_ID_8831016,Human_RBP_ID_13413296,Human_RBP_ID_19028742,Human_RBP_ID_21978382,Human_RBP_ID_26336994 RMVar_hsa_circ_123026,RMVar_hsa_circ_332875,RMVar_hsa_circ_191247,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_375571,RMVar_hsa_circ_191249,RMVar_hsa_circ_191250 80644 RMVar_ID_80644 Human_SNP_ID_655717956 m1A Human chr19 + 2272803 2272803 2272803 GCGAGCCGACCATGTCTTCATTTGCTTCCACAAGAACCGCGAGGACAGAGGTAGGTGACCCGTAT GCGAGCCGACCATGTCTTCATTTGCTTCCACAGGAACCGCGAGGACAGAGGTAGGTGACCCGTAT A G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:2272726..2273250 26863196 MeRIP-seq:(Medium) rs768291790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517841,Human_RBP_ID_914172,Human_RBP_ID_1557685,Human_RBP_ID_1881975,Human_RBP_ID_5192630,Human_RBP_ID_19088588,Human_RBP_ID_22069439,Human_RBP_ID_26814897 Human_Splice_Rec_1935414,Human_Splice_Rec_1935415,Human_Splice_Rec_1935424,Human_Splice_Rec_1935425,Human_Splice_Rec_1935432,Human_Splice_Rec_1935433,Human_Splice_Rec_1935440,Human_Splice_Rec_1935441,Human_Splice_Rec_1935446,Human_Splice_Rec_1935452,Human_Splice_Rec_1935454,Human_Splice_Rec_1935458,Human_Splice_Rec_1935459,Human_Splice_Rec_1935461 Human_miRNA_ID_2917552 RMVar_hsa_circ_123026,RMVar_hsa_circ_332875,RMVar_hsa_circ_191247,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_375571,RMVar_hsa_circ_191249,RMVar_hsa_circ_191250,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252 80645 RMVar_ID_80645 Human_SNP_ID_655717965 m1A Human chr19 + 2272819 2272819 2272819 TTCATTTGCTTCCACAAGAACCGCGAGGACAGAGGTAGGTGACCCGTATCGCCTGCAGTAGGGTG TTCATTTGCTTCCACAAGAACCGCGAGGACAGGGGTAGGTGACCCGTATCGCCTGCAGTAGGGTG A G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2272680..2272861 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_914172,Human_RBP_ID_5192630,Human_RBP_ID_5375037,Human_RBP_ID_19088588,Human_RBP_ID_22069439,Human_RBP_ID_26814898 Human_Splice_Rec_1935414,Human_Splice_Rec_1935415,Human_Splice_Rec_1935424,Human_Splice_Rec_1935425,Human_Splice_Rec_1935432,Human_Splice_Rec_1935433,Human_Splice_Rec_1935440,Human_Splice_Rec_1935441,Human_Splice_Rec_1935446,Human_Splice_Rec_1935452,Human_Splice_Rec_1935454,Human_Splice_Rec_1935458,Human_Splice_Rec_1935459,Human_Splice_Rec_1935461 RMVar_hsa_circ_123026,RMVar_hsa_circ_332875,RMVar_hsa_circ_191247,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_375571,RMVar_hsa_circ_191249,RMVar_hsa_circ_191250,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252 80646 RMVar_ID_80646 Human_SNP_ID_655718171 m1A Human chr19 + 2273095 2273092 2273095 GGCCTACACGTTCGAGAGAGAGTCTTCGGGAGAGGAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC GGCCTACACGTTCGAGAGAGAGTCTTCGGG___GGAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC GAGA G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2273026..2273250 26863196 MeRIP-seq:(Medium) rs1217721603 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_53041,Human_RBP_ID_239518,Human_RBP_ID_517842,Human_RBP_ID_1557688,Human_RBP_ID_1881976,Human_RBP_ID_3565770,Human_RBP_ID_4514093,Human_RBP_ID_5499203,Human_RBP_ID_6732081,Human_RBP_ID_8481367,Human_RBP_ID_8831019,Human_RBP_ID_13413348,Human_RBP_ID_17655771,Human_RBP_ID_22533274,Human_RBP_ID_22968209,Human_RBP_ID_23130877,Human_RBP_ID_23175383,Human_RBP_ID_23788966,Human_RBP_ID_27271421 RMVar_hsa_circ_123026,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_85488,RMVar_hsa_circ_191249,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252,RMVar_hsa_circ_191253 80647 RMVar_ID_80647 Human_SNP_ID_655718173 m1A Human chr19 + 2273095 2273093 2273096 GGCCTACACGTTCGAGAGAGAGTCTTCGGGAGAGGAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC GGCCTACACGTTCGAGAGAGAGTCTTCGGGA___GAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC AGAG A AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2273026..2273250 26863196 MeRIP-seq:(Medium) rs367654384 Functional Loss DEL dbSNP153,HGVD 32..34 33 - - - Human_RBP_ID_53041,Human_RBP_ID_239518,Human_RBP_ID_517842,Human_RBP_ID_1557688,Human_RBP_ID_1881976,Human_RBP_ID_3565770,Human_RBP_ID_4514093,Human_RBP_ID_5499203,Human_RBP_ID_6732081,Human_RBP_ID_8481367,Human_RBP_ID_8831019,Human_RBP_ID_13413348,Human_RBP_ID_17655771,Human_RBP_ID_22533274,Human_RBP_ID_22968209,Human_RBP_ID_23130877,Human_RBP_ID_23175383,Human_RBP_ID_23788966,Human_RBP_ID_27271421 RMVar_hsa_circ_123026,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_85488,RMVar_hsa_circ_191249,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252,RMVar_hsa_circ_191253 80648 RMVar_ID_80648 Human_SNP_ID_655718221 m1A Human chr19 + 2273145 2273145 2273145 GCCTCGGGGCTGGGCATCCGGCCCCTGGGGCCACCCCTTGTCAGCCGGGTGGGTAGGAACCGTAG GCCTCGGGGCTGGGCATCCGGCCCCTGGGGCCCCCCCTTGTCAGCCGGGTGGGTAGGAACCGTAG A C AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2273045..2273221 26863196 MeRIP-seq:(Medium) rs763716322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517845,Human_RBP_ID_1014035,Human_RBP_ID_1188121,Human_RBP_ID_1557689,Human_RBP_ID_1881979,Human_RBP_ID_3565773,Human_RBP_ID_4514096,Human_RBP_ID_5194184,Human_RBP_ID_6732086,Human_RBP_ID_8481367,Human_RBP_ID_13413351,Human_RBP_ID_17267397,Human_RBP_ID_17656544,Human_RBP_ID_17918350,Human_RBP_ID_22502067,Human_RBP_ID_22590648,Human_RBP_ID_23788969,Human_RBP_ID_26651676,Human_RBP_ID_27271422,Human_RBP_ID_27675682 Human_miRNA_ID_939923,Human_miRNA_ID_3115271 RMVar_hsa_circ_123026,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_85488,RMVar_hsa_circ_191249,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252,RMVar_hsa_circ_191253 80649 RMVar_ID_80649 Human_SNP_ID_655718222 m1A Human chr19 + 2273145 2273145 2273145 GCCTCGGGGCTGGGCATCCGGCCCCTGGGGCCACCCCTTGTCAGCCGGGTGGGTAGGAACCGTAG GCCTCGGGGCTGGGCATCCGGCCCCTGGGGCCTCCCCTTGTCAGCCGGGTGGGTAGGAACCGTAG A T AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2273045..2273221 26863196 MeRIP-seq:(Medium) rs763716322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517845,Human_RBP_ID_1014035,Human_RBP_ID_1188121,Human_RBP_ID_1557689,Human_RBP_ID_1881979,Human_RBP_ID_3565773,Human_RBP_ID_4514096,Human_RBP_ID_5194184,Human_RBP_ID_6732086,Human_RBP_ID_8481367,Human_RBP_ID_13413351,Human_RBP_ID_17267397,Human_RBP_ID_17656544,Human_RBP_ID_17918350,Human_RBP_ID_22502067,Human_RBP_ID_22590648,Human_RBP_ID_23788969,Human_RBP_ID_26651676,Human_RBP_ID_27271422,Human_RBP_ID_27675682 Human_miRNA_ID_939923,Human_miRNA_ID_3115271 RMVar_hsa_circ_123026,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_85488,RMVar_hsa_circ_191249,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252,RMVar_hsa_circ_191253 80650 RMVar_ID_80650 Human_SNP_ID_655718233 m1A Human chr19 - 2273153 2273153 2273153 GAGCGAGTCTACGGTTCCTACCCACCCGGCTGACAAGGGGTGGCCCCAGGGGCCGGATGCCCAGC GAGCGAGTCTACGGTTCCTACCCACCCGGCTGGCAAGGGGTGGCCCCAGGGGCCGGATGCCCAGC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2273108..2273195 26863410 MeRIP-seq:(Medium) rs1211009206 Functional Loss SNV dbSNP153 33..33 33 - - - 80651 RMVar_ID_80651 Human_SNP_ID_655734809 m1A Human chr19 + 2324130 2324130 2324130 GCCTGCCTCGGCCGCCACCCCACTCACCTCGCATGTACTCAATGGTGCCGTCCAGCACAAGGTTG GCCTGCCTCGGCCGCCACCCCACTCACCTCGCGTGTACTCAATGGTGCCGTCCAGCACAAGGTTG A G AC005258.1 Ensembl:ENSG00000273734 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2324126..2324200 26863196 MeRIP-seq:(Medium) rs760032057 Functional Loss SNV dbSNP153 33..33 33 - - - 80652 RMVar_ID_80652 Human_SNP_ID_655735165 m1A Human chr19 + 2325343 2325343 2325343 CCCCTCCACTGCCCTGCAGGCTCCTGCAGCCGAGGCCCAGCAGCAGCTCCACCTCTGCGCTCACT CCCCTCCACTGCCCTGCAGGCTCCTGCAGCCGCGGCCCAGCAGCAGCTCCACCTCTGCGCTCACT A C AC005258.1 Ensembl:ENSG00000273734 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2325331..2325790 26863196 MeRIP-seq:(Medium) rs935267139 Functional Loss SNV dbSNP153 33..33 33 - - - 80653 RMVar_ID_80653 Human_SNP_ID_655735172 m1A Human chr19 + 2325361 2325361 2325361 GGCTCCTGCAGCCGAGGCCCAGCAGCAGCTCCACCTCTGCGCTCACTGAGGGGCGTCCCGCAGCC GGCTCCTGCAGCCGAGGCCCAGCAGCAGCTCCCCCTCTGCGCTCACTGAGGGGCGTCCCGCAGCC A C AC005258.1 Ensembl:ENSG00000273734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2325346..2325505 26863196 MeRIP-seq:(Medium) rs12984128 Functional Loss SNV dbSNP153 33..33 33 - - - 80654 RMVar_ID_80654 Human_SNP_ID_655735173 m1A Human chr19 + 2325361 2325361 2325361 GGCTCCTGCAGCCGAGGCCCAGCAGCAGCTCCACCTCTGCGCTCACTGAGGGGCGTCCCGCAGCC GGCTCCTGCAGCCGAGGCCCAGCAGCAGCTCCGCCTCTGCGCTCACTGAGGGGCGTCCCGCAGCC A G AC005258.1 Ensembl:ENSG00000273734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2325346..2325505 26863196 MeRIP-seq:(Medium) rs12984128 Functional Loss SNV dbSNP153 33..33 33 - - - 80655 RMVar_ID_80655 Human_SNP_ID_655736324 m1A Human chr19 - 2328747 2328747 2328747 TCACCTGGGCCGCGAGGAGCAGAAAGGCCGCCAAAAGCCGCGCCAGCGCAGCCGCCACCGCTGCC TCACCTGGGCCGCGAGGAGCAGAAAGGCCGCCGAAAGCCGCGCCAGCGCAGCCGCCACCGCTGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2328702..2328818 26863196 MeRIP-seq:(Medium) rs553331698 Functional Loss SNV dbSNP153 33..33 33 - - - 80656 RMVar_ID_80656 Human_SNP_ID_655737668 m1A Human chr19 - 2333200 2333199 2333201 CATCCCCACCCTCCTCCTGCTCCCCTCCCAGCAGAGTCTAGTCCAGCCGCCCGCACCTGCCATCC CATCCCCACCCTCCTCCTGCTCCCCTCCCAG__GAGTCTAGTCCAGCCGCCCGCACCTGCCATCC CTG C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2333198..2333350 26863196 MeRIP-seq:(Medium) rs1568427563 Functional Loss DEL dbSNP153 32..33 33 - - - 80657 RMVar_ID_80657 Human_SNP_ID_655738139 m1A Human chr19 + 2334659 2334659 2334659 ACGTGGTCTCCCAGGCCGGGGGCCCCGAAGGCAAAGACTACTGCATCCTCTACAACCCGCAGTGG ACGTGGTCTCCCAGGCCGGGGGCCCCGAAGGCGAAGACTACTGCATCCTCTACAACCCGCAGTGG A G AC005258.1,SPPL2B Ensembl:ENSG00000273734,Ensembl:ENSG00000005206 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2334585..2334700 26863196 MeRIP-seq:(Medium) rs1484672931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517893,Human_RBP_ID_4557873,Human_RBP_ID_27466141 Human_Splice_Rec_1935464,Human_Splice_Rec_1935465,Human_Splice_Rec_1935518,Human_Splice_Rec_1935519,Human_Splice_Rec_1935524,Human_Splice_Rec_1935525,Human_Splice_Rec_1935541,Human_Splice_Rec_1935554,Human_Splice_Rec_1935555,Human_Splice_Rec_1935582,Human_Splice_Rec_1935583,Human_Splice_Rec_1935610,Human_Splice_Rec_1935611,Human_Splice_Rec_1935625 80658 RMVar_ID_80658 Human_SNP_ID_655738565 m1A Human chr19 - 2335462 2335462 2335462 GAAAGGAGGCGGGGCCTGAAGGATGCAATGAGAAAGGAGGCGGGGCCTGAAGCATGCAGTGGGAA GAAAGGAGGCGGGGCCTGAAGGATGCAATGAGGAAGGAGGCGGGGCCTGAAGCATGCAGTGGGAA T C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2335411..2335739 26863196 MeRIP-seq:(Medium) rs575062006 Functional Loss SNV dbSNP153 33..33 33 - - - 80659 RMVar_ID_80659 Human_SNP_ID_655738566 m1A Human chr19 - 2335464 2335464 2335464 GGGAAAGGAGGCGGGGCCTGAAGGATGCAATGAGAAAGGAGGCGGGGCCTGAAGCATGCAGTGGG GGGAAAGGAGGCGGGGCCTGAAGGATGCAATGGGAAAGGAGGCGGGGCCTGAAGCATGCAGTGGG T C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2335460..2335754 26863196 MeRIP-seq:(Medium) rs1418813422 Functional Loss SNV dbSNP153 33..33 33 - - - 80660 RMVar_ID_80660 Human_SNP_ID_655739609 m1A Human chr19 + 2337584 2337584 2337584 CCTTCTATGAGAAAGTGAGGCTGGCCCAGGGCAGCGGAGCACGCGGGCTGCTCATCGTCAGCAGG CCTTCTATGAGAAAGTGAGGCTGGCCCAGGGCGGCGGAGCACGCGGGCTGCTCATCGTCAGCAGG A G AC005258.1,SPPL2B Ensembl:ENSG00000273734,Ensembl:ENSG00000005206 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2337537..2337903 26863196 MeRIP-seq:(Medium) rs1233403151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18470388 Human_Splice_Rec_1935467,Human_Splice_Rec_1935527,Human_Splice_Rec_1935543,Human_Splice_Rec_1935557,Human_Splice_Rec_1935585,Human_Splice_Rec_1935613,Human_Splice_Rec_1935629 80661 RMVar_ID_80661 Human_SNP_ID_655739816 m1A Human chr19 + 2338131 2338131 2338131 GGTTGAGAGCTGGGGGCCTGGCAGGGCTGGTCACAGCACAGGGACATGCCGACTGCTGGGCTGGG GGTTGAGAGCTGGGGGCCTGGCAGGGCTGGTCCCAGCACAGGGACATGCCGACTGCTGGGCTGGG A C AC005258.1,SPPL2B Ensembl:ENSG00000273734,Ensembl:ENSG00000005206 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2338094..2338271 26863196 MeRIP-seq:(Medium) rs970764042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1935516 80662 RMVar_ID_80662 Human_SNP_ID_655739817 m1A Human chr19 + 2338131 2338131 2338131 GGTTGAGAGCTGGGGGCCTGGCAGGGCTGGTCACAGCACAGGGACATGCCGACTGCTGGGCTGGG GGTTGAGAGCTGGGGGCCTGGCAGGGCTGGTCGCAGCACAGGGACATGCCGACTGCTGGGCTGGG A G AC005258.1,SPPL2B Ensembl:ENSG00000273734,Ensembl:ENSG00000005206 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2338094..2338271 26863196 MeRIP-seq:(Medium) rs970764042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1935516 80663 RMVar_ID_80663 Human_SNP_ID_655740522 m1A Human chr19 + 2339874 2339874 2339874 GCGCGACGATGGGCCCGAGAAGCAGGAGGACGAGGCGGTGGACGTGACGCCGGTGATGACCTGCG GCGCGACGATGGGCCCGAGAAGCAGGAGGACGCGGCGGTGGACGTGACGCCGGTGATGACCTGCG A C AC005258.1,SPPL2B Ensembl:ENSG00000273734,Ensembl:ENSG00000005206 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2339768..2339975 26863196 MeRIP-seq:(Medium) rs774355784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241015,Human_RBP_ID_3955920,Human_RBP_ID_18995928,Human_RBP_ID_26335138,Human_RBP_ID_27839193 Human_Splice_Rec_1935472,Human_Splice_Rec_1935473,Human_Splice_Rec_1935532,Human_Splice_Rec_1935533,Human_Splice_Rec_1935548,Human_Splice_Rec_1935549,Human_Splice_Rec_1935562,Human_Splice_Rec_1935563,Human_Splice_Rec_1935590,Human_Splice_Rec_1935591,Human_Splice_Rec_1935618,Human_Splice_Rec_1935619,Human_Splice_Rec_1935634,Human_Splice_Rec_1935638,Human_Splice_Rec_1935639,Human_Splice_Rec_1935644,Human_Splice_Rec_1935645,Human_Splice_Rec_1935653 RMVar_hsa_circ_16616,RMVar_hsa_circ_39462,RMVar_hsa_circ_36009 80664 RMVar_ID_80664 Human_SNP_ID_655740568 m1A Human chr19 - 2339959 2339959 2339959 GGCCCACCCGCCCGGGGCCGCGCACCGAGGAGATCGTAGAAATAGTAGAGCAGCACCAGCATGGA GGCCCACCCGCCCGGGGCCGCGCACCGAGGAGGTCGTAGAAATAGTAGAGCAGCACCAGCATGGA T C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:2339940..2340066 26863196 MeRIP-seq:(Medium) rs1609752 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 80665 RMVar_ID_80665 Human_SNP_ID_655741636 m1A Human chr19 - 2342189 2342188 2342190 ACTTCGGCTCTCTCCTGGCCCCACGAAGCCCCAGAGTCCCCTCCCCGCTGGCCCCTGCCCCCAAT ACTTCGGCTCTCTCCTGGCCCCACGAAGCCC__GAGTCCCCTCCCCGCTGGCCCCTGCCCCCAAT CTG C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2342140..2342270 26863196 MeRIP-seq:(Medium) rs1356065807 Functional Loss DEL dbSNP153 32..33 33 - - - 80666 RMVar_ID_80666 Human_SNP_ID_655746878 m1A Human chr19 + 2353208 2353208 2353208 GTCCCCGGTAACCCAGCCTGGCGCCTCGGCCTAGGGGAGGGGTGAGACGCTCGCTGCCGTGCCCG GTCCCCGGTAACCCAGCCTGGCGCCTCGGCCTGGGGGAGGGGTGAGACGCTCGCTGCCGTGCCCG A G SPPL2B Ensembl:ENSG00000005206 Protein coding stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2353160..2353909 32194978 MeRIP-seq:(Medium) rs888585423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4514347,Human_RBP_ID_26471678 RMVar_hsa_circ_84366,RMVar_hsa_circ_94701,RMVar_hsa_circ_191257,RMVar_hsa_circ_191258 80667 RMVar_ID_80667 Human_SNP_ID_655769780 m1A Human chr19 + 2418007 2418007 2418007 TGGCCTTTCTGGCTCTTTCCCTGGTAGCCACCAAGCCCGAGCTCCTGCAGAAGGCGTCCGTGGGC TGGCCTTTCTGGCTCTTTCCCTGGTAGCCACCCAGCCCGAGCTCCTGCAGAAGGCGTCCGTGGGC A C TMPRSS9 Ensembl:ENSG00000178297 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2417965..2418100 32194978 MeRIP-seq:(Medium) rs1204592271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1935692,Human_Splice_Rec_1935726,Human_Splice_Rec_1935776,Human_Splice_Rec_1935804,Human_Splice_Rec_1935820 80668 RMVar_ID_80668 Human_SNP_ID_655769880 m1A Human chr19 + 2418200 2418198 2418201 TATTTCCATGAAATGCCCACAGCCGTTCACCCAGCAGTTCTTTGTGTGCAGACCTAGATTTTTTT TATTTCCATGAAATGCCCACAGCCGTTCACC___CAGTTCTTTGTGTGCAGACCTAGATTTTTTT CCAG C TMPRSS9 Ensembl:ENSG00000178297 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2418016..2418274 26863196 MeRIP-seq:(Medium) rs896276348 Functional Loss DEL dbSNP153 32..34 33 - - - 80669 RMVar_ID_80669 Human_SNP_ID_655769889 m1A Human chr19 - 2418226 2418225 2418226 GAAGGAGGGGGGGAAGGAAAGAAAGGAAAAAAATCTAGGTCTGCACACAAAGAACTGCTGGGTGA GAAGGAGGGGGGGAAGGAAAGAAAGGAAAAAA_TCTAGGTCTGCACACAAAGAACTGCTGGGTGA AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2418118..2422034 26863196 MeRIP-seq:(Medium) rs984350108 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1188161,Human_RBP_ID_17068493,Human_RBP_ID_22978622,Human_RBP_ID_25442958 80670 RMVar_ID_80670 Human_SNP_ID_655771211 m1A Human chr19 - 2419201 2419192 2419202 AGACTCCGTCAGAAAGAAAGAAACAGAGAGAAAGACAGAGAGAGAGAGAGAAGGAAAGGAAAGGA AGACTCCGTCAGAAAGAAAGAAACAGAGAGA__________GAGAGAGAGAAGGAAAGGAAAGGA CTCTCTGTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2419127..2419262 26863196 MeRIP-seq:(Medium) rs1266723842 Functional Loss DEL dbSNP153 32..41 33 - - - 80671 RMVar_ID_80671 Human_SNP_ID_655773619 m1A Human chr19 - 2425231 2425208 2425231 TTCGCGCACCGAGCCCCAGCCGGTGATGACGCAGCGCGTGCCGTCCGGGGGTCGCGGCGCGGGCT TTCGCGCACCGAGCCCCAGCCGGTGATGACGC_______________________GGCGCGGGCT CGCGACCCCCGGACGGCACGCGCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:2425194..2425326 26863196 MeRIP-seq:(Medium) rs1395532570 Functional Loss DEL dbSNP153 33..55 33 - - - 80672 RMVar_ID_80672 Human_SNP_ID_655774810 m1A Human chr19 - 2427326 2427325 2427327 GACGTCGCGGCTAAAGCCTCGCGTGTCTCCACAGAGGATGACGGACAAGTGTTTCCGGAAGTGTA GACGTCGCGGCTAAAGCCTCGCGTGTCTCCA__GAGGATGACGGACAAGTGTTTCCGGAAGTGTA CTG C TIMM13 Ensembl:ENSG00000099800 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2427301..2427325 26863196 MeRIP-seq:(Medium) rs760414936 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_908273,Human_RBP_ID_4514575,Human_RBP_ID_5275396,Human_RBP_ID_22476379 Human_Splice_Rec_1935823,Human_Splice_Rec_1935827 80673 RMVar_ID_80673 Human_SNP_ID_655774888 m1A Human chr19 - 2427463 2427463 2427463 CAGCGGGAAGCTGGACCCAGGGCTCATAATGGAGCAGGTGAAAGTGCAGATCGCCGTGGCCAACG CAGCGGGAAGCTGGACCCAGGGCTCATAATGGTGCAGGTGAAAGTGCAGATCGCCGTGGCCAACG T A TIMM13 Ensembl:ENSG00000099800 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2427324..2427575 26863196 MeRIP-seq:(Medium) rs1414631934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518138,Human_RBP_ID_773458,Human_RBP_ID_1014169,Human_RBP_ID_1558034,Human_RBP_ID_1882185,Human_RBP_ID_4514576,Human_RBP_ID_5115972,Human_RBP_ID_9085623,Human_RBP_ID_9353650,Human_RBP_ID_13416857,Human_RBP_ID_23789507,Human_RBP_ID_24374766,Human_RBP_ID_26987325,Human_RBP_ID_27271612 Human_Splice_Rec_1935821,Human_Splice_Rec_1935825 80674 RMVar_ID_80674 Human_SNP_ID_655774897 m1A Human chr19 - 2427481 2427481 2427481 CGATTTCGGGGGCTCCGGCAGCGGGAAGCTGGACCCAGGGCTCATAATGGAGCAGGTGAAAGTGC CGATTTCGGGGGCTCCGGCAGCGGGAAGCTGGCCCCAGGGCTCATAATGGAGCAGGTGAAAGTGC T G TIMM13 Ensembl:ENSG00000099800 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2426601..2427746 32194978 MeRIP-seq:(Medium) rs779235677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241180,Human_RBP_ID_518138,Human_RBP_ID_773458,Human_RBP_ID_1014169,Human_RBP_ID_1558034,Human_RBP_ID_4514576,Human_RBP_ID_5115972,Human_RBP_ID_8481712,Human_RBP_ID_9353650,Human_RBP_ID_13416860,Human_RBP_ID_17655784,Human_RBP_ID_18412232,Human_RBP_ID_18726255,Human_RBP_ID_22448148,Human_RBP_ID_23130917,Human_RBP_ID_23789507,Human_RBP_ID_24374766,Human_RBP_ID_26987325,Human_RBP_ID_27271612,Human_RBP_ID_27466291,Human_RBP_ID_27675978 Human_Splice_Rec_1935821,Human_Splice_Rec_1935825 80675 RMVar_ID_80675 Human_SNP_ID_655774934 m1A Human chr19 - 2427529 2427529 2427529 GCCTCGGTCCGGTTGACTTTGCGGAGCCATGGAGGGCGGCTTCGGCTCCGATTTCGGGGGCTCCG GCCTCGGTCCGGTTGACTTTGCGGAGCCATGGGGGGCGGCTTCGGCTCCGATTTCGGGGGCTCCG T C TIMM13 Ensembl:ENSG00000099800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2427239..2427598 26863196 MeRIP-seq:(Medium) rs1555682217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54997,Human_RBP_ID_4514578,Human_RBP_ID_5115972,Human_RBP_ID_8481713,Human_RBP_ID_23789508 Human_Splice_Rec_1935825 80676 RMVar_ID_80676 Human_SNP_ID_655774938 m1A Human chr19 - 2427533 2427533 2427533 CGCGGCCTCGGTCCGGTTGACTTTGCGGAGCCATGGAGGGCGGCTTCGGCTCCGATTTCGGGGGC CGCGGCCTCGGTCCGGTTGACTTTGCGGAGCCGTGGAGGGCGGCTTCGGCTCCGATTTCGGGGGC T C TIMM13 Ensembl:ENSG00000099800 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2427399..2427575 26863196 MeRIP-seq:(Medium) rs1555682219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54997,Human_RBP_ID_1558036,Human_RBP_ID_4514578,Human_RBP_ID_8481713,Human_RBP_ID_18726256,Human_RBP_ID_23789508 Human_Splice_Rec_1935825 80677 RMVar_ID_80677 Human_SNP_ID_655775797 m1A Human chr19 - 2429952 2429952 2429952 ATGCGTCTATCCATACTGTGCTTTTATCTGTGATTTTCTCGCTGAAACCATGTTTCTCAGACAGG ATGCGTCTATCCATACTGTGCTTTTATCTGTGGTTTTCTCGCTGAAACCATGTTTCTCAGACAGG T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:2429866..2429964 26863410 MeRIP-seq:(Medium) rs952676184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518196,Human_RBP_ID_1558077,Human_RBP_ID_1882208,Human_RBP_ID_2561568,Human_RBP_ID_3566187,Human_RBP_ID_6734187,Human_RBP_ID_8481749,Human_RBP_ID_8831198,Human_RBP_ID_13417011,Human_RBP_ID_17267516,Human_RBP_ID_17498544,Human_RBP_ID_18302653,Human_RBP_ID_18726278,Human_RBP_ID_23789533,Human_RBP_ID_24484034,Human_RBP_ID_26471694,Human_RBP_ID_27271640 Human_miRNA_ID_1517460,Human_miRNA_ID_2732247,Human_miRNA_ID_2732248 RMVar_hsa_circ_79017,RMVar_hsa_circ_97104,RMVar_hsa_circ_105069,RMVar_hsa_circ_115714,RMVar_hsa_circ_120423,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191264,RMVar_hsa_circ_191265,RMVar_hsa_circ_191263,RMVar_hsa_circ_191261,RMVar_hsa_circ_378009,RMVar_hsa_circ_191259,RMVar_hsa_circ_191266 80678 RMVar_ID_80678 Human_SNP_ID_655775893 m1A Human chr19 - 2430228 2430228 2430228 CCCGCAGTTCAGTTCCTGACTGTGCAAGGCCAACAGGGCAGGGGAGGGGAAGACCTGGGGAAGGA CCCGCAGTTCAGTTCCTGACTGTGCAAGGCCAGCAGGGCAGGGGAGGGGAAGACCTGGGGAAGGA T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2430178..2430350 26863196 MeRIP-seq:(Medium) rs751872464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203036,Human_RBP_ID_3566193,Human_RBP_ID_3955930,Human_RBP_ID_4514711,Human_RBP_ID_5145922,Human_RBP_ID_5319940,Human_RBP_ID_6734201,Human_RBP_ID_8197319,Human_RBP_ID_8481753,Human_RBP_ID_9293188,Human_RBP_ID_13417033,Human_RBP_ID_17387123,Human_RBP_ID_17918826,Human_RBP_ID_18192693,Human_RBP_ID_18726281,Human_RBP_ID_22370884,Human_RBP_ID_22810260,Human_RBP_ID_23789535,Human_RBP_ID_26335141,Human_RBP_ID_26466690 Human_Splice_Rec_1935860 Human_miRNA_ID_976172,Human_miRNA_ID_3091225,Human_miRNA_ID_3091226 RMVar_hsa_circ_79017,RMVar_hsa_circ_97104,RMVar_hsa_circ_105069,RMVar_hsa_circ_115714,RMVar_hsa_circ_120423,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191264,RMVar_hsa_circ_191265,RMVar_hsa_circ_191263,RMVar_hsa_circ_191261,RMVar_hsa_circ_378009,RMVar_hsa_circ_191259,RMVar_hsa_circ_191266 80679 RMVar_ID_80679 Human_SNP_ID_655777008 m1A Human chr19 - 2433070 2433070 2433070 GCAGGGGACAAGGTGACTGGAATGACCGGGGCATGGGGGTAACGGGGTGACCCAGCTGATGGGGG GCAGGGGACAAGGTGACTGGAATGACCGGGGCGTGGGGGTAACGGGGTGACCCAGCTGATGGGGG T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2433068..2433138 26863196 MeRIP-seq:(Medium) rs1247536391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79017,RMVar_hsa_circ_97104,RMVar_hsa_circ_115714,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191263,RMVar_hsa_circ_191261,RMVar_hsa_circ_378009,RMVar_hsa_circ_191259,RMVar_hsa_circ_191266,RMVar_hsa_circ_17977 80680 RMVar_ID_80680 Human_SNP_ID_655777565 m1A Human chr19 + 2434442 2434442 2434442 TCTCCGTCATCTCCTGCTCCTTGGCGTCCAGCATCTTCCGGAACTTGTCCCGCTCCCCGGCCATG TCTCCGTCATCTCCTGCTCCTTGGCGTCCAGCTTCTTCCGGAACTTGTCCCGCTCCCCGGCCATG A T lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2434272..2434475;chr19:2434350..2434483 26863196 MeRIP-seq:(Medium) rs1370989745 Functional Loss SNV dbSNP153 33..33 33 - - - 80681 RMVar_ID_80681 Human_SNP_ID_655777755 m1A Human chr19 - 2434877 2434877 2434877 ACAGCGCCAAGCTGAGCTCTGACCAGAACGACAAGGCGGCCAGTGCGGCTCGCGAGGAGCTGAAG ACAGCGCCAAGCTGAGCTCTGACCAGAACGACGAGGCGGCCAGTGCGGCTCGCGAGGAGCTGAAG T C LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2434826..2434926 26863196 MeRIP-seq:(Medium) rs867858000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280162,Human_RBP_ID_4565037,Human_RBP_ID_8481786,Human_RBP_ID_18726303 Human_Splice_Rec_1935846,Human_Splice_Rec_1935847,Human_Splice_Rec_1935861,Human_Splice_Rec_1935870,Human_Splice_Rec_1935871 Human_miRNA_ID_2156367,Human_miRNA_ID_2159927 RMVar_hsa_circ_79017,RMVar_hsa_circ_115714,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191261,RMVar_hsa_circ_191259,RMVar_hsa_circ_27735,RMVar_hsa_circ_17977,RMVar_hsa_circ_1551 80682 RMVar_ID_80682 Human_SNP_ID_655777907 m1A Human chr19 - 2435128 2435128 2435128 GACGCGGCGGCGGCACGAGCGGCGCCTGGTGGAGGTGGACAGCAGCCGGCAGCAGGAGTACGACT GACGCGGCGGCGGCACGAGCGGCGCCTGGTGGGGGTGGACAGCAGCCGGCAGCAGGAGTACGACT T C LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2435001..2436962 26863196 MeRIP-seq:(Medium) rs757881858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240684,Human_RBP_ID_6734472,Human_RBP_ID_8831259,Human_RBP_ID_18192696,Human_RBP_ID_22448149,Human_RBP_ID_23175512,Human_RBP_ID_23789600 Human_Splice_Rec_1935844,Human_Splice_Rec_1935868,Human_Splice_Rec_1935874 Human_miRNA_ID_2017068 RMVar_hsa_circ_79017,RMVar_hsa_circ_115714,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191261,RMVar_hsa_circ_191259,RMVar_hsa_circ_27735,RMVar_hsa_circ_17977,RMVar_hsa_circ_1551 80683 RMVar_ID_80683 Human_SNP_ID_655777908 m1A Human chr19 + 2435131 2435131 2435131 CGTACTCCTGCTGCCGGCTGCTGTCCACCTCCACCAGGCGCCGCTCGTGCCGCCGCCGCGTCTCC CGTACTCCTGCTGCCGGCTGCTGTCCACCTCCTCCAGGCGCCGCTCGTGCCGCCGCCGCGTCTCC A T lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2434940..2436859 32194978 MeRIP-seq:(Medium) rs779447432 Functional Loss SNV dbSNP153 33..33 33 - - - 80684 RMVar_ID_80684 Human_SNP_ID_655779018 m1A Human chr19 + 2438232 2438232 2438232 TGCAGGCTCTGGCAGCGGTTCTCCAGGTCCACACGCATCAGCGTCTCCTTCTCCAGCTGCTTTTT TGCAGGCTCTGGCAGCGGTTCTCCAGGTCCACGCGCATCAGCGTCTCCTTCTCCAGCTGCTTTTT A G lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2438126..2456975 26863196 MeRIP-seq:(Medium) rs367692230 Functional Loss SNV dbSNP153 33..33 33 - - - 80685 RMVar_ID_80685 Human_SNP_ID_655779036 m1A Human chr19 - 2438271 2438271 2438271 TCCTGTGTCTCCCAGGCCGAGGACGGTCATGCAGTGGCCAAAAAGCAGCTGGAGAAGGAGACGCT TCCTGTGTCTCCCAGGCCGAGGACGGTCATGCCGTGGCCAAAAAGCAGCTGGAGAAGGAGACGCT T G LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2437039..2456950 26863196 MeRIP-seq:(Medium) rs758691307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1014204,Human_RBP_ID_4514836,Human_RBP_ID_5372758,Human_RBP_ID_9291682,Human_RBP_ID_18440925,Human_RBP_ID_18995951,Human_RBP_ID_19091471,Human_RBP_ID_26784967 Human_Splice_Rec_1935842 RMVar_hsa_circ_79017,RMVar_hsa_circ_115714,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191261,RMVar_hsa_circ_191259,RMVar_hsa_circ_17977,RMVar_hsa_circ_1551,RMVar_hsa_circ_66067,RMVar_hsa_circ_302570,RMVar_hsa_circ_191268 80686 RMVar_ID_80686 Human_SNP_ID_655780852 m1A Human chr19 - 2444416 2444416 2444416 AGAGATTGGGAAGCTGAGGGCAGAGTTGGACGAGGTCAACAAGAGGTGAGTGGTCACGGCTGGGC AGAGATTGGGAAGCTGAGGGCAGAGTTGGACGTGGTCAACAAGAGGTGAGTGGTCACGGCTGGGC T A LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2438115..2456950 26863196 MeRIP-seq:(Medium) rs1295248694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8060,Human_RBP_ID_1014208,Human_RBP_ID_1882264,Human_RBP_ID_3566254,Human_RBP_ID_4565051,Human_RBP_ID_5375062,Human_RBP_ID_5588326,Human_RBP_ID_6734522,Human_RBP_ID_8831269,Human_RBP_ID_13417290,Human_RBP_ID_17918898,Human_RBP_ID_18192699,Human_RBP_ID_18726318,Human_RBP_ID_22742305,Human_RBP_ID_22978647,Human_RBP_ID_23789650,Human_RBP_ID_24374640,Human_RBP_ID_26334776 Human_Splice_Rec_1935839 RMVar_hsa_circ_79017,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191259,RMVar_hsa_circ_17977,RMVar_hsa_circ_1551,RMVar_hsa_circ_66067 80687 RMVar_ID_80687 Human_SNP_ID_655780861 m1A Human chr19 - 2444448 2444448 2444448 GAGACGGCTCGAGAGCGTGCCCGGCTGCAGATAGAGATTGGGAAGCTGAGGGCAGAGTTGGACGA GAGACGGCTCGAGAGCGTGCCCGGCTGCAGATGGAGATTGGGAAGCTGAGGGCAGAGTTGGACGA T C LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2437157..2456900 32194978 MeRIP-seq:(Medium) rs1281920468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8060,Human_RBP_ID_1882265,Human_RBP_ID_4565052,Human_RBP_ID_6734524,Human_RBP_ID_9294065,Human_RBP_ID_9380057,Human_RBP_ID_13417290,Human_RBP_ID_17935154,Human_RBP_ID_23789650,Human_RBP_ID_24374640,Human_RBP_ID_26334776 Human_Splice_Rec_1935838,Human_Splice_Rec_1935839 Human_miRNA_ID_2233490 RMVar_hsa_circ_79017,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191259,RMVar_hsa_circ_17977,RMVar_hsa_circ_1551,RMVar_hsa_circ_66067 80688 RMVar_ID_80688 Human_SNP_ID_655784703 m1A Human chr19 - 2456894 2456894 2456894 CGCCGAGCCCGGGCCGCCGTCGGGAGCAGCGCAGGCCGCGAGCCGCCGCCACCATGGCCACGCCG CGCCGAGCCCGGGCCGCCGTCGGGAGCAGCGCGGGCCGCGAGCCGCCGCCACCATGGCCACGCCG T C LMNB2 Ensembl:ENSG00000176619 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:2456803..2456959 26863410 MeRIP-seq:(Medium) rs1312287823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4514874,Human_RBP_ID_5238438,Human_RBP_ID_8839631,Human_RBP_ID_9328272,Human_RBP_ID_22069450,Human_RBP_ID_26334777 RMVar_hsa_circ_96966,RMVar_hsa_circ_191259 80689 RMVar_ID_80689 Human_SNP_ID_655784711 m1A Human chr19 + 2456907 2456907 2456907 GTGGCGGCGGCTCGCGGCCTGCGCTGCTCCCGACGGCGGCCCGGGCTCGGCGGGCTCATTCAATC GTGGCGGCGGCTCGCGGCCTGCGCTGCTCCCGGCGGCGGCCCGGGCTCGGCGGGCTCATTCAATC A G lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:2456826..2456918 26863410 MeRIP-seq:(Medium) rs1365379023 Functional Loss SNV dbSNP153 33..33 33 - - - 80690 RMVar_ID_80690 Human_SNP_ID_655784712 m1A Human chr19 + 2456907 2456907 2456907 GTGGCGGCGGCTCGCGGCCTGCGCTGCTCCCGACGGCGGCCCGGGCTCGGCGGGCTCATTCAATC GTGGCGGCGGCTCGCGGCCTGCGCTGCTCCCGTCGGCGGCCCGGGCTCGGCGGGCTCATTCAATC A T lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:2456826..2456918 26863410 MeRIP-seq:(Medium) rs1365379023 Functional Loss SNV dbSNP153 33..33 33 - - - 80691 RMVar_ID_80691 Human_SNP_ID_655790821 m1A Human chr19 - 2476597 2476597 2476597 CATTCATCAACTTGGCCGACTCGTACACCCCCACTGTGAGGCGATCCTGGCGCTGAGCGGCCACC CATTCATCAACTTGGCCGACTCGTACACCCCCGCTGTGAGGCGATCCTGGCGCTGAGCGGCCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2476551..2476625 32194978 MeRIP-seq:(Medium) rs767719964 Functional Loss SNV dbSNP153 33..33 33 - - - 80692 RMVar_ID_80692 Human_SNP_ID_655790822 m1A Human chr19 - 2476597 2476597 2476597 CATTCATCAACTTGGCCGACTCGTACACCCCCACTGTGAGGCGATCCTGGCGCTGAGCGGCCACC CATTCATCAACTTGGCCGACTCGTACACCCCCCCTGTGAGGCGATCCTGGCGCTGAGCGGCCACC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2476551..2476625 32194978 MeRIP-seq:(Medium) rs767719964 Functional Loss SNV dbSNP153 33..33 33 - - - 80693 RMVar_ID_80693 Human_SNP_ID_655810423 m1A Human chr19 - 2539978 2539975 2539978 GAAGAAAGAAAAAAGGAAGGAAAGAGAGAGAGAAGGAGGGAGGGAGGAAGGAAGGAAGGCAGGAA GAAGAAAGAAAAAAGGAAGGAAAGAGAGAGAG___GAGGGAGGGAGGAAGGAAGGAAGGCAGGAA CCTT C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2539951..2540024 26863196 MeRIP-seq:(Medium) rs1214265276 Functional Loss DEL dbSNP153 33..35 33 - - - 80694 RMVar_ID_80694 Human_SNP_ID_655810428 m1A Human chr19 - 2539978 2539978 2539978 GAAGAAAGAAAAAAGGAAGGAAAGAGAGAGAGAAGGAGGGAGGGAGGAAGGAAGGAAGGCAGGAA GAAGAAAGAAAAAAGGAAGGAAAGAGAGAGAGGAGGAGGGAGGGAGGAAGGAAGGAAGGCAGGAA T C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2539951..2540024 26863196 MeRIP-seq:(Medium) rs990378122 Functional Loss SNV dbSNP153 33..33 33 - - - 80695 RMVar_ID_80695 Human_SNP_ID_655810440 m1A Human chr19 - 2540001 2540001 2540001 AGCCAGAGAGAAAGAGAAAGAAAGAAGAAAGAAAAAAGGAAGGAAAGAGAGAGAGAAGGAGGGAG AGCCAGAGAGAAAGAGAAAGAAAGAAGAAAGAGAAAAGGAAGGAAAGAGAGAGAGAAGGAGGGAG T C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2539881..2540028 26863196 MeRIP-seq:(Medium) rs931249707 Functional Loss SNV dbSNP153 33..33 33 - - - 80696 RMVar_ID_80696 Human_SNP_ID_655810514 m1A Human chr19 - 2540124 2540120 2540124 GAAAGAAAGAGAGAGAGAGACGGAAGGAAGGAAGGAGAAAAGAAAAGAAAGAAATTGAGAAAGAA GAAAGAAAGAGAGAGAGAGACGGAAGGAAGGA____GAAAAGAAAAGAAAGAAATTGAGAAAGAA CTCCT C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2540097..2540184 26863196 MeRIP-seq:(Medium) rs112722136 Functional Loss DEL dbSNP153 33..36 33 - - - 80697 RMVar_ID_80697 Human_SNP_ID_655861798 m1A Human chr19 - 2702670 2702670 2702670 GGGGCGGAGGGTTCGGCTGCGCGGCGGGGCTGAGGCGGCCGCGGGGCCCGAGCGCAGGTAAGGGC GGGGCGGAGGGTTCGGCTGCGCGGCGGGGCTGTGGCGGCCGCGGGGCCCGAGCGCAGGTAAGGGC T A GNG7 Ensembl:ENSG00000176533 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2702482..2702712 26863196 MeRIP-seq:(Medium) rs1296265663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582727,Human_RBP_ID_18420827 Human_Splice_Rec_1935901 80698 RMVar_ID_80698 Human_SNP_ID_655871753 m1A Human chr19 - 2732662 2732662 2732662 AGGCCGCGTCCCCCGGCCGCGCGTCCCCCAAGAGCGAGCACTGTGGCCCTGGGCCACCACCTGTG AGGCCGCGTCCCCCGGCCGCGCGTCCCCCAAGTGCGAGCACTGTGGCCCTGGGCCACCACCTGTG T A AC006538.2,SLC39A3 Ensembl:ENSG00000267001,Ensembl:ENSG00000141873 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2732613..2732772 26863196 MeRIP-seq:(Medium) rs950311078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518340,Human_RBP_ID_9328273,Human_RBP_ID_17656560 Human_miRNA_ID_1996837,Human_miRNA_ID_2229330,Human_miRNA_ID_2505300,Human_miRNA_ID_2574827 RMVar_hsa_circ_89042,RMVar_hsa_circ_106069,RMVar_hsa_circ_191274,RMVar_hsa_circ_191275 80699 RMVar_ID_80699 Human_SNP_ID_655871910 m1A Human chr19 - 2732987 2732987 2732987 TGCGGGACGCGGCCAAGCTGGCGGTCACCGTAAGCGCCATGATCCCCCTGGGCATCGGCCTGGGC TGCGGGACGCGGCCAAGCTGGCGGTCACCGTACGCGCCATGATCCCCCTGGGCATCGGCCTGGGC T G AC006538.2,SLC39A3 Ensembl:ENSG00000267001,Ensembl:ENSG00000141873 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr19:2732885..2733084;chr19:2732936..2733016 26863410,26863196 MeRIP-seq:(Medium) rs1568299108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4515087,Human_RBP_ID_5115976,Human_RBP_ID_22446313,Human_RBP_ID_22763185 RMVar_hsa_circ_89042,RMVar_hsa_circ_106069,RMVar_hsa_circ_191274,RMVar_hsa_circ_191275 80700 RMVar_ID_80700 Human_SNP_ID_655878491 m1A Human chr19 - 2755312 2755312 2755312 CCGCGGCTCAGGAGCCGTCCTGGGTGCATAGGACCAGTTTCTGTGACTTTTCTCCAGTTGGGCAT CCGCGGCTCAGGAGCCGTCCTGGGTGCATAGGTCCAGTTTCTGTGACTTTTCTCCAGTTGGGCAT T A SGTA Ensembl:ENSG00000104969 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2755251..2755325 32194978 MeRIP-seq:(Medium) rs1260175649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518360,Human_RBP_ID_1558204,Human_RBP_ID_1882272,Human_RBP_ID_3566285,Human_RBP_ID_8481855,Human_RBP_ID_9085685,Human_RBP_ID_13417706,Human_RBP_ID_18302706,Human_RBP_ID_23789838,Human_RBP_ID_27466404,Human_RBP_ID_27562329 Human_miRNA_ID_541828,Human_miRNA_ID_967021,Human_miRNA_ID_1798271,Human_miRNA_ID_2191831,Human_miRNA_ID_2249602,Human_miRNA_ID_2921308 RMVar_hsa_circ_89203,RMVar_hsa_circ_106078,RMVar_hsa_circ_107457,RMVar_hsa_circ_100221,RMVar_hsa_circ_191277,RMVar_hsa_circ_191278,RMVar_hsa_circ_191279,RMVar_hsa_circ_191276 80701 RMVar_ID_80701 Human_SNP_ID_655882494 m1A Human chr19 - 2767639 2767639 2767639 TGGAGACTGCGTTTGGGGTGACGGTAGAAGACAGTGACCTTGCGCTCCCTCAGACTCTGCCGGAG TGGAGACTGCGTTTGGGGTGACGGTAGAAGACGGTGACCTTGCGCTCCCTCAGACTCTGCCGGAG T C SGTA Ensembl:ENSG00000104969 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2767544..2767649 26863196 MeRIP-seq:(Medium) rs533871028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518391,Human_RBP_ID_1558236,Human_RBP_ID_3955937,Human_RBP_ID_6734664,Human_RBP_ID_8831288,Human_RBP_ID_13417929,Human_RBP_ID_18995957,Human_RBP_ID_27271830 Human_Splice_Rec_1935958,Human_Splice_Rec_1935959,Human_Splice_Rec_1935988,Human_Splice_Rec_1935989,Human_Splice_Rec_1935998 Human_miRNA_ID_2515315 RMVar_hsa_circ_89203,RMVar_hsa_circ_34117,RMVar_hsa_circ_191279,RMVar_hsa_circ_284375,RMVar_hsa_circ_295597,RMVar_hsa_circ_332189 80702 RMVar_ID_80702 Human_SNP_ID_655883122 m1A Human chr19 - 2769684 2769684 2769684 CCTCCCAGGGGGAACAAGACGGGTCCCCAAGAAGTCCCTGGGGGGAGTCCTCTGCAAGTCCTGTG CCTCCCAGGGGGAACAAGACGGGTCCCCAAGATGTCCCTGGGGGGAGTCCTCTGCAAGTCCTGTG T A SGTA Ensembl:ENSG00000104969 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2769671..2769950 26863196 MeRIP-seq:(Medium) rs1294228774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3585293,Human_RBP_ID_8195593,Human_RBP_ID_22358763,Human_RBP_ID_22718788 80703 RMVar_ID_80703 Human_SNP_ID_655886550 m1A Human chr19 - 2780226 2780207 2780226 GGGCAGAGTGTTCACAGAAGGTAGTGGGTAAGAGCGGGCCCTTCCTACTGGGGTGTGAGGAGGTA GGGCAGAGTGTTCACAGAAGGTAGTGGGTAAG___________________GGTGTGAGGAGGTA CCCAGTAGGAAGGGCCCGCT C SGTA Ensembl:ENSG00000104969 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2780219..2780365 26863196 MeRIP-seq:(Medium) rs1431733905 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_13418146 80704 RMVar_ID_80704 Human_SNP_ID_655886556 m1A Human chr19 - 2780226 2780226 2780226 GGGCAGAGTGTTCACAGAAGGTAGTGGGTAAGAGCGGGCCCTTCCTACTGGGGTGTGAGGAGGTA GGGCAGAGTGTTCACAGAAGGTAGTGGGTAAGGGCGGGCCCTTCCTACTGGGGTGTGAGGAGGTA T C SGTA Ensembl:ENSG00000104969 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2780219..2780365 26863196 MeRIP-seq:(Medium) rs1255809232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13418146 80705 RMVar_ID_80705 Human_SNP_ID_655886570 m1A Human chr19 - 2780280 2780280 2780280 CCGGCTCTCCTGCCCTGCTGTTGGTGAGAAGCACCGTGGATTTGGGATGGAGTTGGGCAGAGTGT CCGGCTCTCCTGCCCTGCTGTTGGTGAGAAGCGCCGTGGATTTGGGATGGAGTTGGGCAGAGTGT T C SGTA Ensembl:ENSG00000104969 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2780276..2780359 26863196 MeRIP-seq:(Medium) rs1406925462 Functional Loss SNV dbSNP153 33..33 33 - - - 80706 RMVar_ID_80706 Human_SNP_ID_655888135 m1A Human chr19 + 2785627 2785627 2785627 TGGCCGAGGTGGCTGGACGCGTAGCAGGTGGAAGGAGGGAGGGAGCCGCAGGCGCAGACCCACCC TGGCCGAGGTGGCTGGACGCGTAGCAGGTGGAGGGAGGGAGGGAGCCGCAGGCGCAGACCCACCC A G THOP1 Ensembl:ENSG00000172009 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:2785541..2785628 26863410 MeRIP-seq:(Medium) rs765737168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518398,Human_RBP_ID_769680,Human_RBP_ID_913988,Human_RBP_ID_3955939,Human_RBP_ID_4515249,Human_RBP_ID_5117654,Human_RBP_ID_13418254,Human_RBP_ID_18192706,Human_RBP_ID_18995959,Human_RBP_ID_22977974,Human_RBP_ID_23789901 Human_Splice_Rec_1936001,Human_Splice_Rec_1936025,Human_Splice_Rec_1936035,Human_Splice_Rec_1936045 RMVar_hsa_circ_103837,RMVar_hsa_circ_191284 80707 RMVar_ID_80707 Human_SNP_ID_655888140 m1A Human chr19 + 2785638 2785638 2785638 GCTGGACGCGTAGCAGGTGGAAGGAGGGAGGGAGCCGCAGGCGCAGACCCACCCGCCATGAAGCC GCTGGACGCGTAGCAGGTGGAAGGAGGGAGGGGGCCGCAGGCGCAGACCCACCCGCCATGAAGCC A G THOP1 Ensembl:ENSG00000172009 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:2785542..2785675 26863196 MeRIP-seq:(Medium) rs758853902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518398,Human_RBP_ID_769680,Human_RBP_ID_913988,Human_RBP_ID_3955939,Human_RBP_ID_4515249,Human_RBP_ID_5117654,Human_RBP_ID_18192706,Human_RBP_ID_18995959,Human_RBP_ID_22977974,Human_RBP_ID_23789901 Human_Splice_Rec_1936001,Human_Splice_Rec_1936025,Human_Splice_Rec_1936035,Human_Splice_Rec_1936045 RMVar_hsa_circ_103837,RMVar_hsa_circ_191284 80708 RMVar_ID_80708 Human_SNP_ID_655888154 m1A Human chr19 + 2785663 2785663 2785663 GGGAGGGAGCCGCAGGCGCAGACCCACCCGCCATGAAGCCCCCCGCAGGTACCGACTACCCCGCT GGGAGGGAGCCGCAGGCGCAGACCCACCCGCCGTGAAGCCCCCCGCAGGTACCGACTACCCCGCT A G THOP1 Ensembl:ENSG00000172009 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:2785518..2785748 26863196 MeRIP-seq:(Medium) rs1454430793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913988,Human_RBP_ID_3955939,Human_RBP_ID_4557889,Human_RBP_ID_5117654,Human_RBP_ID_18192706,Human_RBP_ID_18995959,Human_RBP_ID_22977974 Human_Splice_Rec_1936001,Human_Splice_Rec_1936025,Human_Splice_Rec_1936035,Human_Splice_Rec_1936045 RMVar_hsa_circ_103837,RMVar_hsa_circ_191284 80709 RMVar_ID_80709 Human_SNP_ID_655889556 m1A Human chr19 + 2790513 2790513 2790513 GGGACCTGAGTGCCCAGCAGATAGAGGAGCGCACCAGGGAGCTCATCGAGCAGACCAAGCGCGTG GGGACCTGAGTGCCCAGCAGATAGAGGAGCGCGCCAGGGAGCTCATCGAGCAGACCAAGCGCGTG A G THOP1 Ensembl:ENSG00000172009 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2790463..2790614 32194978 MeRIP-seq:(Medium) rs780912516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9294066,Human_RBP_ID_27271848 Human_Splice_Rec_1936002,Human_Splice_Rec_1936026,Human_Splice_Rec_1936038,Human_Splice_Rec_1936046 Human_miRNA_ID_2894773 RMVar_hsa_circ_52424,RMVar_hsa_circ_103837,RMVar_hsa_circ_363211,RMVar_hsa_circ_191284,RMVar_hsa_circ_305086,RMVar_hsa_circ_191285 80710 RMVar_ID_80710 Human_SNP_ID_655890821 m1A Human chr19 - 2794756 2794754 2794756 GGGAAGTCAAGGATATTCCTCTGAACTAAAACAGGGGAGACCAGGGAGACAGGTGTGAGAACAGG GGGAAGTCAAGGATATTCCTCTGAACTAAAAC__GGGAGACCAGGGAGACAGGTGTGAGAACAGG CCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2794751..2794800 26863196 MeRIP-seq:(Medium) rs753845694 Functional Loss DEL dbSNP153 33..34 33 - - - 80711 RMVar_ID_80711 Human_SNP_ID_655891265 m1A Human chr19 + 2796137 2796137 2796137 AGGCCCGAGGCTGCGCGGTACCTGGAGCGGCTAATCAAGCTGGGCCGGAGAAATGGGCTTCACCT AGGCCCGAGGCTGCGCGGTACCTGGAGCGGCTCATCAAGCTGGGCCGGAGAAATGGGCTTCACCT A C THOP1 Ensembl:ENSG00000172009 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:2796036..2796136 32194978 MeRIP-seq:(Medium) rs750356105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518404,Human_RBP_ID_4515269,Human_RBP_ID_18995963,Human_RBP_ID_22977575,Human_RBP_ID_23789924 Human_Splice_Rec_1936006,Human_Splice_Rec_1936007,Human_Splice_Rec_1936030,Human_Splice_Rec_1936031,Human_Splice_Rec_1936042,Human_Splice_Rec_1936043,Human_Splice_Rec_1936049 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_305086,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_343208,RMVar_hsa_circ_304380,RMVar_hsa_circ_191286 80712 RMVar_ID_80712 Human_SNP_ID_655893194 m1A Human chr19 + 2802442 2802442 2802442 CCCACCTCCCGACACCCCCACCTCCCAACACCAACACCTCCCGACACCCCCACCTCCCGACACCA CCCACCTCCCGACACCCCCACCTCCCAACACCCACACCTCCCGACACCCCCACCTCCCGACACCA A C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2802435..2802614 26863196 MeRIP-seq:(Medium) rs1347747747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 80713 RMVar_ID_80713 Human_SNP_ID_655893204 m1A Human chr19 + 2802475 2802459 2802475 ACACCTCCCGACACCCCCACCTCCCGACACCAACACCTCCCGACACCAACACCTCCCGACACCAA ACACCTCCCGACACCCC________________CACCTCCCGACACCAACACCTCCCGACACCAA CCACCTCCCGACACCAA C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2802473..2802624 26863196 MeRIP-seq:(Medium) rs1422963095 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_26784984 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 80714 RMVar_ID_80714 Human_SNP_ID_655893209 m1A Human chr19 + 2802475 2802472 2802475 ACACCTCCCGACACCCCCACCTCCCGACACCAACACCTCCCGACACCAACACCTCCCGACACCAA ACACCTCCCGACACCCCCACCTCCCGACAC___CACCTCCCGACACCAACACCTCCCGACACCAA CCAA C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2802473..2802624 26863196 MeRIP-seq:(Medium) rs1191239336 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_26784984 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 80715 RMVar_ID_80715 Human_SNP_ID_655893213 m1A Human chr19 + 2802475 2802475 2802475 ACACCTCCCGACACCCCCACCTCCCGACACCAACACCTCCCGACACCAACACCTCCCGACACCAA ACACCTCCCGACACCCCCACCTCCCGACACCACCACCTCCCGACACCAACACCTCCCGACACCAA A C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2802473..2802624 26863196 MeRIP-seq:(Medium) rs1254390591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26784984 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 80716 RMVar_ID_80716 Human_SNP_ID_655895852 m1A Human chr19 + 2810353 2810353 2810353 CAGCGGGACCCACGTGGAGCGGGACTTTGTGGAGGCGCCGTCGCAGATGCTGGAGAACTGGGTGT CAGCGGGACCCACGTGGAGCGGGACTTTGTGGGGGCGCCGTCGCAGATGCTGGAGAACTGGGTGT A G THOP1 Ensembl:ENSG00000172009 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2810280..2810456 26863196 MeRIP-seq:(Medium) rs1446398617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518414,Human_RBP_ID_8831309,Human_RBP_ID_9328281,Human_RBP_ID_9380068,Human_RBP_ID_18994040,Human_RBP_ID_22069480,Human_RBP_ID_22233135,Human_RBP_ID_22977577,Human_RBP_ID_26334778 Human_Splice_Rec_1936018,Human_Splice_Rec_1936060,Human_Splice_Rec_1936070,Human_Splice_Rec_1936082,Human_Splice_Rec_1936084,Human_Splice_Rec_1936088,Human_Splice_Rec_1936094,Human_Splice_Rec_1936102,Human_Splice_Rec_1936118 Human_miRNA_ID_2442316 RMVar_hsa_circ_363211,RMVar_hsa_circ_191285,RMVar_hsa_circ_350995,RMVar_hsa_circ_191289,RMVar_hsa_circ_372653 80717 RMVar_ID_80717 Human_SNP_ID_655896413 m1A Human chr19 - 2811814 2811771 2811814 CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCCATTCAGGACGCCCTCCCTGTCCCCAGTCCCCGC CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCC_________________________________ CGGCAAGGTACGCGGGGACTGGGGACAGGGAGGGCGTCCTGAAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2811751..2811875;chr19:2811751..2812016;chr19:2811727..2812001;chr19:2811745..2811875 26863196 MeRIP-seq:(Medium) rs1568327266 Functional Loss DEL dbSNP153 33..65 33 - - - 80718 RMVar_ID_80718 Human_SNP_ID_655896461 m1A Human chr19 - 2811814 2811814 2811814 CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCCATTCAGGACGCCCTCCCTGTCCCCAGTCCCCGC CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCCGTTCAGGACGCCCTCCCTGTCCCCAGTCCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2811751..2811875;chr19:2811751..2812016;chr19:2811727..2812001;chr19:2811745..2811875 26863196 MeRIP-seq:(Medium) rs8109048 Functional Loss SNV dbSNP153 33..33 33 - - - 80719 RMVar_ID_80719 Human_SNP_ID_655896627 m1A Human chr19 + 2812123 2812122 2812124 CGAGTCCTTCCGGGATCTGCGTGATCGGCCTCAGAGCCATGGGCTGAGACAGACCCTTCTCTGGA CGAGTCCTTCCGGGATCTGCGTGATCGGCCTC__AGCCATGGGCTGAGACAGACCCTTCTCTGGA CAG C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2812119..2813518 32194978 MeRIP-seq:(Medium) rs1238731324 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18489490,Human_RBP_ID_19094597 Human_Splice_Rec_1936108 80720 RMVar_ID_80720 Human_SNP_ID_655897085 m1A Human chr19 - 2813422 2813422 2813422 TCTCTAGCCGGGTGGGCCACGACCGGGTGGGGACAGACAATGACAAGAGGCAAGACAGCCGCTCA TCTCTAGCCGGGTGGGCCACGACCGGGTGGGGGCAGACAATGACAAGAGGCAAGACAGCCGCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2813129..2813465 26863196 MeRIP-seq:(Medium) rs1188743983 Functional Loss SNV dbSNP153 33..33 33 - - - 80721 RMVar_ID_80721 Human_SNP_ID_655899029 m1A Human chr19 + 2819967 2819967 2819967 CCTGCGGGGGGCGTCCGCTCCGAGCGCCGAGGAGCCGAGCGGAGGAGGCGTCCCAGGGACACGCA CCTGCGGGGGGCGTCCGCTCCGAGCGCCGAGGGGCCGAGCGGAGGAGGCGTCCCAGGGACACGCA A G ZNF554 Ensembl:ENSG00000172006 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2819920..2820123 26863196 MeRIP-seq:(Medium) rs2741993 Functional Loss SNV dbSNP153 33..33 33 - - - 80722 RMVar_ID_80722 Human_SNP_ID_655905679 m1A Human chr19 - 2841537 2841537 2841537 CCGGGGCGATTTCTTCGCTACCGGCGCAGGTGAGCGCGACAGGAACCGGGACGCCAGGGACCGCT CCGGGGCGATTTCTTCGCTACCGGCGCAGGTGCGCGCGACAGGAACCGGGACGCCAGGGACCGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2841512..2841699 26863196 MeRIP-seq:(Medium) rs369537107 Functional Loss SNV dbSNP153 33..33 33 - - - 80723 RMVar_ID_80723 Human_SNP_ID_655924091 m1A Human chr19 + 2901012 2901012 2901012 CTTTCAGCTGCGCCGGCCGCGAGGCCACGGAGAGCTCGCCTTGGAGAGCCCAGGAGCAGGGGAGA CTTTCAGCTGCGCCGGCCGCGAGGCCACGGAGGGCTCGCCTTGGAGAGCCCAGGAGCAGGGGAGA A G ZNF57 Ensembl:ENSG00000171970 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2900963..2901127 26863196 MeRIP-seq:(Medium) rs765941879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1936195,Human_Splice_Rec_1936197 80724 RMVar_ID_80724 Human_SNP_ID_655924108 m1A Human chr19 - 2901054 2901054 2901054 CCGACCGTCCCCTGGCTCTGCTCCTGCCTCGCACTCACCATGTCTCCCCTGCTCCTGGGCTCTCC CCGACCGTCCCCTGGCTCTGCTCCTGCCTCGCGCTCACCATGTCTCCCCTGCTCCTGGGCTCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2901010..2901304 26863196 MeRIP-seq:(Medium) rs764393208 Functional Loss SNV dbSNP153 33..33 33 - - - 80725 RMVar_ID_80725 Human_SNP_ID_655924109 m1A Human chr19 - 2901054 2901054 2901054 CCGACCGTCCCCTGGCTCTGCTCCTGCCTCGCACTCACCATGTCTCCCCTGCTCCTGGGCTCTCC CCGACCGTCCCCTGGCTCTGCTCCTGCCTCGCCCTCACCATGTCTCCCCTGCTCCTGGGCTCTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2901010..2901304 26863196 MeRIP-seq:(Medium) rs764393208 Functional Loss SNV dbSNP153 33..33 33 - - - 80726 RMVar_ID_80726 Human_SNP_ID_655938427 m1A Human chr19 - 2944553 2944550 2944553 TTGTGGGGACAGCAGAGGTGGTCAGGGGCTTGAGGCAATTTAAGTGGACAGTAGAGGTTTAAGGG TTGTGGGGACAGCAGAGGTGGTCAGGGGCTTG___CAATTTAAGTGGACAGTAGAGGTTTAAGGG GCCT G ZNF77 Ensembl:ENSG00000175691 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2944546..2944675 26863196 MeRIP-seq:(Medium) rs1162396440 Functional Loss DEL dbSNP153 33..35 33 - - - 80727 RMVar_ID_80727 Human_SNP_ID_655938500 m1A Human chr19 - 2944761 2944761 2944761 GGCGGCAGGAACCGGCTTCCGCCCGAGTTCGCAGCCGGAGAAAGCTGAGGGACGCGCGGGGCGGC GGCGGCAGGAACCGGCTTCCGCCCGAGTTCGCTGCCGGAGAAAGCTGAGGGACGCGCGGGGCGGC T A ZNF77 Ensembl:ENSG00000175691 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2944711..2944800 26863196 MeRIP-seq:(Medium) rs1180116172 Functional Loss SNV dbSNP153 33..33 33 - - - 80728 RMVar_ID_80728 Human_SNP_ID_655948939 m1A Human chr19 - 2977196 2977196 2977196 AGGCAATTTGGGGTCCCAGCGGGGGCGGGGATATTTAGGAGGGCGTGGGGCTTGAGGCTCAGAGG AGGCAATTTGGGGTCCCAGCGGGGGCGGGGATGTTTAGGAGGGCGTGGGGCTTGAGGCTCAGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2977145..2977247 26863196 MeRIP-seq:(Medium) rs1043739685 Functional Loss SNV dbSNP153 33..33 33 - - - 80729 RMVar_ID_80729 Human_SNP_ID_655957639 m1A Human chr19 - 2997841 2997841 2997841 CCACCGTGTATGAGGTGGTCTACTGAGACATGACCCCCCTTCCTGTACCCGAAGTCCAGACTCCC CCACCGTGTATGAGGTGGTCTACTGAGACATGTCCCCCCTTCCTGTACCCGAAGTCCAGACTCCC T A TLE2 Ensembl:ENSG00000065717 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2997687..2997887 32194978 MeRIP-seq:(Medium) rs759230997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88438,RMVar_hsa_circ_191297 80730 RMVar_ID_80730 Human_SNP_ID_655961678 m1A Human chr19 + 3009699 3009699 3009699 TGAAGGGACTGGACAGAGTCAGGGGGCTCCTCAGGGCTGAGACGGAAGAGTCGGGGACAGGTTTT TGAAGGGACTGGACAGAGTCAGGGGGCTCCTCGGGGCTGAGACGGAAGAGTCGGGGACAGGTTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3009550..3011192 26863196 MeRIP-seq:(Medium) rs1421062008 Functional Loss SNV dbSNP153 33..33 33 - - - 80731 RMVar_ID_80731 Human_SNP_ID_655962960 m1A Human chr19 + 3013747 3013747 3013747 GCCAAGGAGGCTGGACTGTCCACCAGGTCCCGACGGGCAGGAATGCAGATGGGTACCTTTCCGCA GCCAAGGAGGCTGGACTGTCCACCAGGTCCCGCCGGGCAGGAATGCAGATGGGTACCTTTCCGCA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3013635..3013748 26863196 MeRIP-seq:(Medium) rs766252607 Functional Loss SNV dbSNP153 33..33 33 - - - 80732 RMVar_ID_80732 Human_SNP_ID_655963622 m1A Human chr19 - 3015720 3015718 3015721 TCCCTCGCCCCCTGAGAGTCTCGTGGAGGAGGAGCGACCGAGTGGCCCTGGTGGTGGCGGGAAGC TCCCTCGCCCCCTGAGAGTCTCGTGGAGGAG___CGACCGAGTGGCCCTGGTGGTGGCGGGAAGC GCTC G TLE2 Ensembl:ENSG00000065717 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3013794..3019385 32194978 MeRIP-seq:(Medium) rs779003684 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1936390,Human_Splice_Rec_1936391,Human_Splice_Rec_1936426,Human_Splice_Rec_1936427,Human_Splice_Rec_1936462,Human_Splice_Rec_1936463,Human_Splice_Rec_1936500,Human_Splice_Rec_1936501,Human_Splice_Rec_1936540,Human_Splice_Rec_1936541,Human_Splice_Rec_1936578,Human_Splice_Rec_1936579,Human_Splice_Rec_1936618,Human_Splice_Rec_1936619,Human_Splice_Rec_1936628,Human_Splice_Rec_1936629,Human_Splice_Rec_1936644,Human_Splice_Rec_1936645,Human_Splice_Rec_1936654,Human_Splice_Rec_1936655,Human_Splice_Rec_1936672,Human_Splice_Rec_1936673,Human_Splice_Rec_1936684,Human_Splice_Rec_1936685,Human_Splice_Rec_1936696,Human_Splice_Rec_1936697,Human_Splice_Rec_1936706 RMVar_hsa_circ_59038,RMVar_hsa_circ_25549,RMVar_hsa_circ_112097,RMVar_hsa_circ_191301,RMVar_hsa_circ_368497 80733 RMVar_ID_80733 Human_SNP_ID_655963626 m1A Human chr19 - 3015720 3015720 3015720 TCCCTCGCCCCCTGAGAGTCTCGTGGAGGAGGAGCGACCGAGTGGCCCTGGTGGTGGCGGGAAGC TCCCTCGCCCCCTGAGAGTCTCGTGGAGGAGGGGCGACCGAGTGGCCCTGGTGGTGGCGGGAAGC T C TLE2 Ensembl:ENSG00000065717 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3013794..3019385 32194978 MeRIP-seq:(Medium) rs770003592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1936390,Human_Splice_Rec_1936391,Human_Splice_Rec_1936426,Human_Splice_Rec_1936427,Human_Splice_Rec_1936462,Human_Splice_Rec_1936463,Human_Splice_Rec_1936500,Human_Splice_Rec_1936501,Human_Splice_Rec_1936540,Human_Splice_Rec_1936541,Human_Splice_Rec_1936578,Human_Splice_Rec_1936579,Human_Splice_Rec_1936618,Human_Splice_Rec_1936619,Human_Splice_Rec_1936628,Human_Splice_Rec_1936629,Human_Splice_Rec_1936644,Human_Splice_Rec_1936645,Human_Splice_Rec_1936654,Human_Splice_Rec_1936655,Human_Splice_Rec_1936672,Human_Splice_Rec_1936673,Human_Splice_Rec_1936684,Human_Splice_Rec_1936685,Human_Splice_Rec_1936696,Human_Splice_Rec_1936697,Human_Splice_Rec_1936706 RMVar_hsa_circ_59038,RMVar_hsa_circ_25549,RMVar_hsa_circ_112097,RMVar_hsa_circ_191301,RMVar_hsa_circ_368497 80734 RMVar_ID_80734 Human_SNP_ID_655975976 m1A Human chr19 - 3053854 3053854 3053854 CCAAGGAAGACAAGAACGGGCACGATGGTGACACCCACCAGGAGGATGATGGCGAGAAGTCGGAT CCAAGGAAGACAAGAACGGGCACGATGGTGACCCCCACCAGGAGGATGATGGCGAGAAGTCGGAT T G TLE5 Ensembl:ENSG00000104964 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3053759..3053909 26863196 MeRIP-seq:(Medium) rs758128884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518821,Human_RBP_ID_1014398,Human_RBP_ID_1559001,Human_RBP_ID_1883055,Human_RBP_ID_8482554,Human_RBP_ID_17919637,Human_RBP_ID_23790593 RMVar_hsa_circ_79377,RMVar_hsa_circ_107508,RMVar_hsa_circ_88891,RMVar_hsa_circ_191303,RMVar_hsa_circ_191304,RMVar_hsa_circ_191302 80735 RMVar_ID_80735 Human_SNP_ID_655976654 m1A Human chr19 + 3055866 3055866 3055866 TAAGAGGGGCTAGGTCTGGCCAGGGTGGGATGAGCAAAGCCGTGTTCGGGCCCGAGGGCAGCCAG TAAGAGGGGCTAGGTCTGGCCAGGGTGGGATGGGCAAAGCCGTGTTCGGGCCCGAGGGCAGCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3055864..3056069 26863196 MeRIP-seq:(Medium) rs1218822424 Functional Loss SNV dbSNP153 33..33 33 - - - 80736 RMVar_ID_80736 Human_SNP_ID_655977100 m1A Human chr19 - 3056862 3056860 3056862 GGGAATGAACTTGGTTTTCCCCCAGGGGTGACAGGGAGCCATGGGAGGGTTTAGAGCAGGGGAGG GGGAATGAACTTGGTTTTCCCCCAGGGGTGAC__GGAGCCATGGGAGGGTTTAGAGCAGGGGAGG CCT C TLE5 Ensembl:ENSG00000104964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3056859..3056975 26863196 MeRIP-seq:(Medium) rs1208490936 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_34354,RMVar_hsa_circ_79377,RMVar_hsa_circ_107508,RMVar_hsa_circ_103596,RMVar_hsa_circ_191303,RMVar_hsa_circ_191304,RMVar_hsa_circ_322905,RMVar_hsa_circ_191307,RMVar_hsa_circ_191308 80737 RMVar_ID_80737 Human_SNP_ID_655978491 m1A Human chr19 - 3061259 3061259 3061259 CCTGGGCCTGACCCGGGCCGCCCCATCCCTACAGGGCTCCTCGCACCTACCCCAGCAACTCAAAT CCTGGGCCTGACCCGGGCCGCCCCATCCCTACCGGGCTCCTCGCACCTACCCCAGCAACTCAAAT T G TLE5 Ensembl:ENSG00000104964 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:3061226..3061275;chr19:3061251..3061275;chr19:3061176..3061335;chr19:3061176..3061332 26863196,26863410,26863410 MeRIP-seq:(Medium) rs111972928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4565435,Human_RBP_ID_18191739 Human_Splice_Rec_1936755,Human_Splice_Rec_1936767,Human_Splice_Rec_1936779,Human_Splice_Rec_1936797,Human_Splice_Rec_1936807,Human_Splice_Rec_1936819,Human_Splice_Rec_1936831 RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80738 RMVar_ID_80738 Human_SNP_ID_655978583 m1A Human chr19 + 3061400 3061400 3061400 TTCCTGGGCCCGTGTTTACGGCCCCTGGCGCGACCCCACCCGCGCTTCCTGCCCCCCGCCTCTCC TTCCTGGGCCCGTGTTTACGGCCCCTGGCGCGCCCCCACCCGCGCTTCCTGCCCCCCGCCTCTCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:3061395..3062265 32194978 MeRIP-seq:(Medium) rs886820320 Functional Loss SNV dbSNP153 33..33 33 - - - 80739 RMVar_ID_80739 Human_SNP_ID_655978978 m1A Human chr19 - 3062116 3062109 3062116 CCCCCACCCCGGATCCGGGCCCTACGCCCCCGACCCCCGGCTCCCGGCCCCGCGCCCCCCAACCC CCCCCACCCCGGATCCGGGCCCTACGCCCCCG_______GCTCCCGGCCCCGCGCCCCCCAACCC CCGGGGGT C TLE5 Ensembl:ENSG00000104964 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3062111..3062529 26863196 MeRIP-seq:(Medium) rs1338625645 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80740 RMVar_ID_80740 Human_SNP_ID_655978982 m1A Human chr19 - 3062116 3062116 3062116 CCCCCACCCCGGATCCGGGCCCTACGCCCCCGACCCCCGGCTCCCGGCCCCGCGCCCCCCAACCC CCCCCACCCCGGATCCGGGCCCTACGCCCCCGCCCCCCGGCTCCCGGCCCCGCGCCCCCCAACCC T G TLE5 Ensembl:ENSG00000104964 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3062111..3062529 26863196 MeRIP-seq:(Medium) rs1318178978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80741 RMVar_ID_80741 Human_SNP_ID_655979029 m1A Human chr19 - 3062256 3062256 3062256 GGACAAAGGCGCGGCCGCCCGGCGCCCCCAGCAGCCCGAGCCGGGGCGCACAGCCGGGGCGCAGC GGACAAAGGCGCGGCCGCCCGGCGCCCCCAGCCGCCCGAGCCGGGGCGCACAGCCGGGGCGCAGC T G TLE5 Ensembl:ENSG00000104964 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3062151..3062757 26863410 MeRIP-seq:(Medium) rs1373815966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557892,Human_RBP_ID_5117260,Human_RBP_ID_5144925,Human_RBP_ID_5238447,Human_RBP_ID_8198345,Human_RBP_ID_9328283,Human_RBP_ID_17655789,Human_RBP_ID_17934789,Human_RBP_ID_18191741,Human_RBP_ID_18412238,Human_RBP_ID_22592998,Human_RBP_ID_26471737 Human_Splice_Rec_1936753,Human_Splice_Rec_1936795,Human_Splice_Rec_1936817,Human_Splice_Rec_1936829,Human_Splice_Rec_1936833 RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80742 RMVar_ID_80742 Human_SNP_ID_655979030 m1A Human chr19 - 3062259 3062259 3062259 CCGGGACAAAGGCGCGGCCGCCCGGCGCCCCCAGCAGCCCGAGCCGGGGCGCACAGCCGGGGCGC CCGGGACAAAGGCGCGGCCGCCCGGCGCCCCCGGCAGCCCGAGCCGGGGCGCACAGCCGGGGCGC T C TLE5 Ensembl:ENSG00000104964 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3062151..3062465 26863410 MeRIP-seq:(Medium) rs1463754477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557892,Human_RBP_ID_5117260,Human_RBP_ID_5144925,Human_RBP_ID_5238447,Human_RBP_ID_8198345,Human_RBP_ID_9328283,Human_RBP_ID_17655789,Human_RBP_ID_17934789,Human_RBP_ID_18191741,Human_RBP_ID_18412238,Human_RBP_ID_22592998,Human_RBP_ID_26471737 Human_Splice_Rec_1936753,Human_Splice_Rec_1936795,Human_Splice_Rec_1936817,Human_Splice_Rec_1936829,Human_Splice_Rec_1936833 RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80743 RMVar_ID_80743 Human_SNP_ID_655979058 m1A Human chr19 - 3062360 3062360 3062360 GCCCGGGGCGCGCCGGGGCCGGGCGCGCGGGGAGGGGGCGCAGGAAGCGGGCGAGGCCGGGCGCG GCCCGGGGCGCGCCGGGGCCGGGCGCGCGGGGGGGGGGCGCAGGAAGCGGGCGAGGCCGGGCGCG T C TLE5 Ensembl:ENSG00000104964 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr19:3062203..3062500;chr19:3062194..3062500 26863410 MeRIP-seq:(Medium) rs913219885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239555,Human_RBP_ID_825267,Human_RBP_ID_3585304,Human_RBP_ID_3954162,Human_RBP_ID_4557074,Human_RBP_ID_5116566,Human_RBP_ID_5144926,Human_RBP_ID_5239519,Human_RBP_ID_5321104,Human_RBP_ID_5372793,Human_RBP_ID_8197340,Human_RBP_ID_8727992,Human_RBP_ID_8942139,Human_RBP_ID_9328284,Human_RBP_ID_9425087,Human_RBP_ID_17386584,Human_RBP_ID_17670270,Human_RBP_ID_18191741,Human_RBP_ID_19088636,Human_RBP_ID_22426324,Human_RBP_ID_22533072,Human_RBP_ID_22590695,Human_RBP_ID_23257674,Human_RBP_ID_24532748,Human_RBP_ID_26471738,Human_RBP_ID_26784989,Human_RBP_ID_27814898,Human_RBP_ID_27839206 RMVar_hsa_circ_107508,RMVar_hsa_circ_191304,RMVar_hsa_circ_85412,RMVar_hsa_circ_191310 80744 RMVar_ID_80744 Human_SNP_ID_655979080 m1A Human chr19 - 3062419 3062419 3062419 AGCGGGGAGGCGGGCGGCGGGGAGGGGCGGGGAGGGGCGCCGGGCGCGCAGGAAGCGGGGCCCGG AGCGGGGAGGCGGGCGGCGGGGAGGGGCGGGGGGGGGCGCCGGGCGCGCAGGAAGCGGGGCCCGG T C TLE5 Ensembl:ENSG00000104964 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3062151..3062550 26863196 MeRIP-seq:(Medium) rs967438319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770621,Human_RBP_ID_825267,Human_RBP_ID_3582741,Human_RBP_ID_4516314,Human_RBP_ID_5116567,Human_RBP_ID_5144926,Human_RBP_ID_5239519,Human_RBP_ID_8195615,Human_RBP_ID_8233007,Human_RBP_ID_8728312,Human_RBP_ID_8942139,Human_RBP_ID_9328285,Human_RBP_ID_9425088,Human_RBP_ID_18944772,Human_RBP_ID_26471739,Human_RBP_ID_26784989,Human_RBP_ID_27839206 RMVar_hsa_circ_107508,RMVar_hsa_circ_191304 80745 RMVar_ID_80745 Human_SNP_ID_655979093 m1A Human chr19 - 3062444 3062444 3062444 TTAGACAATAGCGGTGGGGCCGGGGAGCGGGGAGGCGGGCGGCGGGGAGGGGCGGGGAGGGGCGC TTAGACAATAGCGGTGGGGCCGGGGAGCGGGGGGGCGGGCGGCGGGGAGGGGCGGGGAGGGGCGC T C TLE5 Ensembl:ENSG00000104964 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3062151..3062526 26863196 MeRIP-seq:(Medium) rs1321511546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107508,RMVar_hsa_circ_191304 80746 RMVar_ID_80746 Human_SNP_ID_655989483 m1A Human chr19 + 3094504 3094504 3094504 CGGGGACCCGGCGGCTCGCCAGGCGGCGGCCGAGGCGGGGCGGGCCGGCCCGGGGCCGAGGGCCG CGGGGACCCGGCGGCTCGCCAGGCGGCGGCCGGGGCGGGGCGGGCCGGCCCGGGGCCGAGGGCCG A G GNA11 Ensembl:ENSG00000088256 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,untreat control chr19:3094376..3094750;chr19:3094410..3094610 26863196,26863410 MeRIP-seq:(Medium) rs1314051618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557076,Human_RBP_ID_9353661,Human_RBP_ID_17131562,Human_RBP_ID_18192713,Human_RBP_ID_22447151 RMVar_hsa_circ_126538,RMVar_hsa_circ_191311 80747 RMVar_ID_80747 Human_SNP_ID_655993001 m1A Human chr19 - 3105844 3105844 3105844 AGAGCCTTCTGTCCACTCCTCACCGCACACCAAGCACCACGGCAGCTTTACTCGTAAAAGCCAAA AGAGCCTTCTGTCCACTCCTCACCGCACACCACGCACCACGGCAGCTTTACTCGTAAAAGCCAAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3105841..3105928 26863196 MeRIP-seq:(Medium) rs368051077 Functional Loss SNV dbSNP153 33..33 33 - - - 80748 RMVar_ID_80748 Human_SNP_ID_655993686 m1A Human chr19 - 3108348 3108347 3108348 CCTCTCACAGCCTCTGCTCTAGAAAGCCCCCAAGCCCCAACACAACTCTCCCTCCGGTACTTTCT CCTCTCACAGCCTCTGCTCTAGAAAGCCCCCA_GCCCCAACACAACTCTCCCTCCGGTACTTTCT CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3108344..3108539 26863196 MeRIP-seq:(Medium) rs553300090 Functional Loss DEL dbSNP153 33..33 33 - - - 80749 RMVar_ID_80749 Human_SNP_ID_655996112 m1A Human chr19 + 3115803 3115803 3115803 GAGGCTGTGAGGGGAGGGGGGGGGTCACGGGGACCGAGGCTGTGAGTGGAGGAGGGGTCATAGGG GAGGCTGTGAGGGGAGGGGGGGGGTCACGGGGGCCGAGGCTGTGAGTGGAGGAGGGGTCATAGGG A G GNA11 Ensembl:ENSG00000088256 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:3115799..3115909;chr19:3115788..3115968 26863196 MeRIP-seq:(Medium) rs1182387762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8195639 RMVar_hsa_circ_43986,RMVar_hsa_circ_126538,RMVar_hsa_circ_191311,RMVar_hsa_circ_320462,RMVar_hsa_circ_121825,RMVar_hsa_circ_191312 80750 RMVar_ID_80750 Human_SNP_ID_655998114 m1A Human chr19 + 3121604 3121592 3121605 GCCCTGCAGCCAGTCACGCGCCCCCACACCGCAGCCCCCCGTGGCTGTCCTTCCAACCCCACGTG GCCCTGCAGCCAGTCACGCGC_____________CCCCCCGTGGCTGTCCTTCCAACCCCACGTG CCCCCACACCGCAG C GNA11 Ensembl:ENSG00000088256 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3121515..3121675 26863196 MeRIP-seq:(Medium) rs1177654176 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_518864,Human_RBP_ID_26466880,Human_RBP_ID_27466621 80751 RMVar_ID_80751 Human_SNP_ID_655998558 m1A Human chr19 - 3122906 3122906 3122906 GCCAGCCCCGTCTCCCCATGGGGCTGATCACCAGAAATGTAGCTGCCCTGACCTGGTCTCCCCTG GCCAGCCCCGTCTCCCCATGGGGCTGATCACCGGAAATGTAGCTGCCCTGACCTGGTCTCCCCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3122855..3123005 32194978 MeRIP-seq:(Medium) rs566440155 Functional Loss SNV dbSNP153 33..33 33 - - - 80752 RMVar_ID_80752 Human_SNP_ID_655998818 m1A Human chr19 + 3123577 3123577 3123577 CGATTTCTCGTGAGTGCCGACCACCTTCTCCGACCATGTTACGCCCGGGCGGCAGCAGCCCCCGG CGATTTCTCGTGAGTGCCGACCACCTTCTCCGGCCATGTTACGCCCGGGCGGCAGCAGCCCCCGG A G GNA11 Ensembl:ENSG00000088256 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3123526..3123661 26863196 MeRIP-seq:(Medium) rs1371968894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518879,Human_RBP_ID_17272250 80753 RMVar_ID_80753 Human_SNP_ID_656019518 m1A Human chr19 - 3185999 3185973 3185999 TCCTGGCCGGCGGCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGACGGCGGCGGCGGCGGCTCCC TCCTGGCCGGCGGCGGGGCCGCGCGGGGCGGC__________________________GGCTCCC CGCCGCCGCCGCCGTCCCGTCCCAGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3185951..3186140 26863196 MeRIP-seq:(Medium) rs1277794302 Functional Loss DEL dbSNP153 33..58 33 - - - 80754 RMVar_ID_80754 Human_SNP_ID_656019530 m1A Human chr19 - 3185987 3185984 3185987 GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGACGGCGGCGGCGGCGGCTCCCGCGGACTCACCT GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGG___GCGGCGGCGGCGGCTCCCGCGGACTCACCT CCGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3185926..3186144;chr19:3185926..3186160;chr19:3185926..3186135 26863196 MeRIP-seq:(Medium) rs981735628 Functional Loss DEL dbSNP153 33..35 33 - - - 80755 RMVar_ID_80755 Human_SNP_ID_656019536 m1A Human chr19 - 3185987 3185987 3185987 GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGACGGCGGCGGCGGCGGCTCCCGCGGACTCACCT GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGTCGGCGGCGGCGGCGGCTCCCGCGGACTCACCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3185926..3186144;chr19:3185926..3186160;chr19:3185926..3186135 26863196 MeRIP-seq:(Medium) rs927117714 Functional Loss SNV dbSNP153 33..33 33 - - - 80756 RMVar_ID_80756 Human_SNP_ID_656019537 m1A Human chr19 - 3185987 3185987 3185987 GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGACGGCGGCGGCGGCGGCTCCCGCGGACTCACCT GCGGGGCCGCGCGGGGCGGCAGCTGGGACGGGGCGGCGGCGGCGGCGGCTCCCGCGGACTCACCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3185926..3186144;chr19:3185926..3186160;chr19:3185926..3186135 26863196 MeRIP-seq:(Medium) rs927117714 Functional Loss SNV dbSNP153 33..33 33 - - - 80757 RMVar_ID_80757 Human_SNP_ID_656019580 m1A Human chr19 - 3186053 3186053 3186053 GCAGACAAGACGCCTTCAGCATGTTCTCCAGCACCTCGCCCGCTTCCTCCAGCATCCTGGCCGGC GCAGACAAGACGCCTTCAGCATGTTCTCCAGCCCCTCGCCCGCTTCCTCCAGCATCCTGGCCGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3185951..3186175 26863410 MeRIP-seq:(Medium) rs1200850258 Functional Loss SNV dbSNP153 33..33 33 - - - 80758 RMVar_ID_80758 Human_SNP_ID_656024096 m1A Human chr19 + 3198779 3198779 3198779 TCTCCAAGCCCCACACACGGGTCACCTGCCCCAGGAACAGCCAGGCCATTCCCCTGCTCTCTATC TCTCCAAGCCCCACACACGGGTCACCTGCCCCCGGAACAGCCAGGCCATTCCCCTGCTCTCTATC A C NCLN Ensembl:ENSG00000125912 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3198775..3198936 26863196 MeRIP-seq:(Medium) rs311621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22661698 GWAS_ID_9602 RMVar_hsa_circ_1690,RMVar_hsa_circ_104705,RMVar_hsa_circ_191318,RMVar_hsa_circ_326247,RMVar_hsa_circ_191315,RMVar_hsa_circ_347628,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_67085,RMVar_hsa_circ_337361,RMVar_hsa_circ_191319,RMVar_hsa_circ_372618,RMVar_hsa_circ_96669,RMVar_hsa_circ_191320,RMVar_hsa_circ_191321,RMVar_hsa_circ_191322 80759 RMVar_ID_80759 Human_SNP_ID_656024097 m1A Human chr19 + 3198779 3198779 3198779 TCTCCAAGCCCCACACACGGGTCACCTGCCCCAGGAACAGCCAGGCCATTCCCCTGCTCTCTATC TCTCCAAGCCCCACACACGGGTCACCTGCCCCGGGAACAGCCAGGCCATTCCCCTGCTCTCTATC A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3198775..3198936 26863196 MeRIP-seq:(Medium) rs311621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22661698 GWAS_ID_9602 RMVar_hsa_circ_1690,RMVar_hsa_circ_104705,RMVar_hsa_circ_191318,RMVar_hsa_circ_326247,RMVar_hsa_circ_191315,RMVar_hsa_circ_347628,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_67085,RMVar_hsa_circ_337361,RMVar_hsa_circ_191319,RMVar_hsa_circ_372618,RMVar_hsa_circ_96669,RMVar_hsa_circ_191320,RMVar_hsa_circ_191321,RMVar_hsa_circ_191322 80760 RMVar_ID_80760 Human_SNP_ID_656024116 m1A Human chr19 - 3198804 3198804 3198804 CCCAGCCCCGTCAGCCGCCCCTGTGGATAGAGAGCAGGGGAATGGCCTGGCTGTTCCTGGGGCAG CCCAGCCCCGTCAGCCGCCCCTGTGGATAGAGTGCAGGGGAATGGCCTGGCTGTTCCTGGGGCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3198801..3198850;chr19:3198801..3198825 26863196 MeRIP-seq:(Medium) rs760023209 Functional Loss SNV dbSNP153 33..33 33 - - - 80761 RMVar_ID_80761 Human_SNP_ID_656024117 m1A Human chr19 - 3198804 3198804 3198804 CCCAGCCCCGTCAGCCGCCCCTGTGGATAGAGAGCAGGGGAATGGCCTGGCTGTTCCTGGGGCAG CCCAGCCCCGTCAGCCGCCCCTGTGGATAGAGGGCAGGGGAATGGCCTGGCTGTTCCTGGGGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3198801..3198850;chr19:3198801..3198825 26863196 MeRIP-seq:(Medium) rs760023209 Functional Loss SNV dbSNP153 33..33 33 - - - 80762 RMVar_ID_80762 Human_SNP_ID_656025006 m1A Human chr19 + 3201255 3201255 3201255 CGGGCGCGGGCCGAGCCGAGGTGGATGAGGAGAGTCCTGGGCTTGGCGGGGCCCCGCAGACCCCA CGGGCGCGGGCCGAGCCGAGGTGGATGAGGAGGGTCCTGGGCTTGGCGGGGCCCCGCAGACCCCA A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3201250..3201422 26863196 MeRIP-seq:(Medium) rs1413715483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9425767,Human_RBP_ID_13424045,Human_RBP_ID_21977493 RMVar_hsa_circ_1690,RMVar_hsa_circ_104705,RMVar_hsa_circ_191318,RMVar_hsa_circ_326247,RMVar_hsa_circ_191315,RMVar_hsa_circ_274659,RMVar_hsa_circ_67085,RMVar_hsa_circ_337361,RMVar_hsa_circ_191319,RMVar_hsa_circ_96669,RMVar_hsa_circ_191320,RMVar_hsa_circ_191321,RMVar_hsa_circ_35201,RMVar_hsa_circ_330824 80763 RMVar_ID_80763 Human_SNP_ID_656025012 m1A Human chr19 - 3201265 3201265 3201265 ACTGATGGCCTGGGGTCTGCGGGGCCCCGCCAAGCCCAGGACTCTCCTCATCCACCTCGGCTCGG ACTGATGGCCTGGGGTCTGCGGGGCCCCGCCAGGCCCAGGACTCTCCTCATCCACCTCGGCTCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:3201260..3201543;chr19:3201249..3201467 26863196 MeRIP-seq:(Medium) rs1046759514 Functional Loss SNV dbSNP153 33..33 33 - - - 80764 RMVar_ID_80764 Human_SNP_ID_656026245 m1A Human chr19 - 3204748 3204748 3204748 AGGGGCCGGGCAGGTGCTGCCGCGCTCACCGCACGTCCATGATGCTGCTGCGCTGGCCGTCACGG AGGGGCCGGGCAGGTGCTGCCGCGCTCACCGCTCGTCCATGATGCTGCTGCGCTGGCCGTCACGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3204665..3205845 26863410 MeRIP-seq:(Medium) rs759011005 Functional Loss SNV dbSNP153 33..33 33 - - - 80765 RMVar_ID_80765 Human_SNP_ID_656027403 m1A Human chr19 + 3207831 3207831 3207831 TCCCTCCCCGGCGGTGGTTGGAACACTGAATTACAGAGCTTTTTTCTGTTGCTCTCCGAGACTGG TCCCTCCCCGGCGGTGGTTGGAACACTGAATTGCAGAGCTTTTTTCTGTTGCTCTCCGAGACTGG A G NCLN Ensembl:ENSG00000125912 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3207630..3208107 26863196 MeRIP-seq:(Medium) rs1434040354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518912,Human_RBP_ID_2562473,Human_RBP_ID_4516807,Human_RBP_ID_8482702,Human_RBP_ID_18303074,Human_RBP_ID_23791307,Human_RBP_ID_26987851,Human_RBP_ID_27272237,Human_RBP_ID_27466666 RMVar_hsa_circ_78683,RMVar_hsa_circ_78192,RMVar_hsa_circ_191326,RMVar_hsa_circ_191329 80766 RMVar_ID_80766 Human_SNP_ID_656027464 m1A Human chr19 + 3207972 3207952 3207973 ACGGACTTGCGGACGAGCCCCCCAGTCCTGGGAGCCGGCCGCCCTCGGTCTGGTGTAAGCACACA ACGGACTTGCGGA_____________________CCGGCCGCCCTCGGTCTGGTGTAAGCACACA ACGAGCCCCCCAGTCCTGGGAG A NCLN Ensembl:ENSG00000125912 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3207927..3208029 26863196 MeRIP-seq:(Medium) rs1276977432 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_518917,Human_RBP_ID_9328305,Human_RBP_ID_17656575,Human_RBP_ID_22590710 Human_miRNA_ID_341753,Human_miRNA_ID_1694116 RMVar_hsa_circ_78683,RMVar_hsa_circ_78192,RMVar_hsa_circ_191326,RMVar_hsa_circ_191329 80767 RMVar_ID_80767 Human_SNP_ID_656027635 m1A Human chr19 + 3208401 3208395 3208402 CGTGGGGGCCTGGCAGGGCCCCTGCCTCCCCGACCCCCGACCCACTGCAAATCCCCGTTCCCCTG CGTGGGGGCCTGGCAGGGCCCCTGCCT_______CCCCGACCCACTGCAAATCCCCGTTCCCCTG TCCCCGAC T NCLN Ensembl:ENSG00000125912 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3208301..3208532 26863410 MeRIP-seq:(Medium) rs1568317042 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_518930,Human_RBP_ID_18727305,Human_RBP_ID_18944780,Human_RBP_ID_23791310 RMVar_hsa_circ_78683,RMVar_hsa_circ_78192,RMVar_hsa_circ_191326,RMVar_hsa_circ_191329 80768 RMVar_ID_80768 Human_SNP_ID_656027647 m1A Human chr19 + 3208408 3208408 3208408 GCCTGGCAGGGCCCCTGCCTCCCCGACCCCCGACCCACTGCAAATCCCCGTTCCCCTGCACTCCT GCCTGGCAGGGCCCCTGCCTCCCCGACCCCCGGCCCACTGCAAATCCCCGTTCCCCTGCACTCCT A G NCLN Ensembl:ENSG00000125912 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3208359..3208521 26863196 MeRIP-seq:(Medium) rs561197559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518930,Human_RBP_ID_18944780,Human_RBP_ID_23791310 RMVar_hsa_circ_78683,RMVar_hsa_circ_78192,RMVar_hsa_circ_191326,RMVar_hsa_circ_191329 80769 RMVar_ID_80769 Human_SNP_ID_656028379 m1A Human chr19 - 3210769 3210769 3210769 GGTCAAAGCCCAAGTCCTCCCCGTGGCCCACCAGGCCCTGCACAACCTGCCCTGTCCCTTCCCCA GGTCAAAGCCCAAGTCCTCCCCGTGGCCCACCGGGCCCTGCACAACCTGCCCTGTCCCTTCCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3210718..3210853 26863196 MeRIP-seq:(Medium) rs1455293494 Functional Loss SNV dbSNP153 33..33 33 - - - 80770 RMVar_ID_80770 Human_SNP_ID_656070772 m1A Human chr19 - 3348187 3348187 3348187 TTACCTCGTTTGATAGAGGAGGCGTCAGATGAAGGAAAGGGGTTATCCAAGGTCACACAATGGGA TTACCTCGTTTGATAGAGGAGGCGTCAGATGAGGGAAAGGGGTTATCCAAGGTCACACAATGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3348011..3348308 26863196 MeRIP-seq:(Medium) rs753286406 Functional Loss SNV dbSNP153 33..33 33 - - - 80771 RMVar_ID_80771 Human_SNP_ID_656073870 m1A Human chr19 - 3359645 3359645 3359645 TGCTGCGAGGAGGCGAGGCCGGCGCCGGAGCGAGCGCGCTCGGTCCCCGGCGAGGGGGGGGCCGC TGCTGCGAGGAGGCGAGGCCGGCGCCGGAGCGGGCGCGCTCGGTCCCCGGCGAGGGGGGGGCCGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3359621..3359772 26863196 MeRIP-seq:(Medium) rs771254258 Functional Loss SNV dbSNP153 33..33 33 - - - 80772 RMVar_ID_80772 Human_SNP_ID_656074793 m1A Human chr19 + 3362373 3362369 3362373 GCTTGTCAAGAAGCGTCCTGTGGGGAGTTGGGAGGGTGTGTTTGTGGCTGTGTGTGTGCCATGTG GCTTGTCAAGAAGCGTCCTGTGGGGAGTT____GGGTGTGTTTGTGGCTGTGTGTGTGCCATGTG TGGGA T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3362368..3362554 26863196 MeRIP-seq:(Medium) rs1333256733 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23792012 80773 RMVar_ID_80773 Human_SNP_ID_656076128 m1A Human chr19 + 3366428 3366428 3366428 GACGGGGGAGAGAGGAAGAGAGAGACGGAGGGAGAGAGGGACAGAGAGCGAGGCGGGCGGCGCGA GACGGGGGAGAGAGGAAGAGAGAGACGGAGGGGGAGAGGGACAGAGAGCGAGGCGGGCGGCGCGA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3366383..3366517 26863196 MeRIP-seq:(Medium) rs1048212842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8195661 80774 RMVar_ID_80774 Human_SNP_ID_656076202 m1A Human chr19 - 3366564 3366547 3366565 GCGCTGAACTTACTGAGTCATTTTTCCAAACCACCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC GCGCTGAACTTACTGAGTCATTTTTCCAAAC__________________AACCCCCCCCCCCGCC TGGGGGGGGCGGGGGGGTG T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:3366526..3366575;chr19:3366551..3366806 26863196 MeRIP-seq:(Medium) rs1266259903 Functional Loss DEL dbSNP153 32..49 33 - - - 80775 RMVar_ID_80775 Human_SNP_ID_656076220 m1A Human chr19 - 3366564 3366564 3366564 GCGCTGAACTTACTGAGTCATTTTTCCAAACCACCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC GCGCTGAACTTACTGAGTCATTTTTCCAAACCGCCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:3366526..3366575;chr19:3366551..3366806 26863196 MeRIP-seq:(Medium) rs866086214 Functional Loss SNV dbSNP153 33..33 33 - - - 80776 RMVar_ID_80776 Human_SNP_ID_656076221 m1A Human chr19 - 3366564 3366564 3366564 GCGCTGAACTTACTGAGTCATTTTTCCAAACCACCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC GCGCTGAACTTACTGAGTCATTTTTCCAAACCCCCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:3366526..3366575;chr19:3366551..3366806 26863196 MeRIP-seq:(Medium) rs866086214 Functional Loss SNV dbSNP153 33..33 33 - - - 80777 RMVar_ID_80777 Human_SNP_ID_656076258 m1A Human chr19 - 3366615 3366615 3366615 GACGAATACATCCCGGGCGCGGCGGGAGGCGCAGGGCCGGCCGGAGCGGGCGCGCTGAACTTACT GACGAATACATCCCGGGCGCGGCGGGAGGCGCGGGGCCGGCCGGAGCGGGCGCGCTGAACTTACT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3366601..3366788 26863196 MeRIP-seq:(Medium) rs1381037710 Functional Loss SNV dbSNP153 33..33 33 - - - 80778 RMVar_ID_80778 Human_SNP_ID_656076278 m1A Human chr19 - 3366642 3366642 3366642 GACCGTACCTGGGTGAGGCAGAGCGGGGACGAATACATCCCGGGCGCGGCGGGAGGCGCAGGGCC GACCGTACCTGGGTGAGGCAGAGCGGGGACGAGTACATCCCGGGCGCGGCGGGAGGCGCAGGGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3366526..3366847 26863196 MeRIP-seq:(Medium) rs1464567890 Functional Loss SNV dbSNP153 33..33 33 - - - 80779 RMVar_ID_80779 Human_SNP_ID_656081521 m1A Human chr19 - 3382136 3382136 3382136 ACAGGACCGGGTGACCGCACTGCGCAGCCTTGACCAGGCGCTCGCCGTCGGTGCTCTCCAGCGGG ACAGGACCGGGTGACCGCACTGCGCAGCCTTGCCCAGGCGCTCGCCGTCGGTGCTCTCCAGCGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3382101..3382150 26863196 MeRIP-seq:(Medium) rs1469697212 Functional Loss SNV dbSNP153 33..33 33 - - - 80780 RMVar_ID_80780 Human_SNP_ID_656081570 m1A Human chr19 - 3382225 3382225 3382225 CCACCACACCTCACCTCGCTCACGCACGAAGTAGGCCAGGTAGAGGTCCAGCTCCTTGACGGCCA CCACCACACCTCACCTCGCTCACGCACGAAGTTGGCCAGGTAGAGGTCCAGCTCCTTGACGGCCA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3382201..3382225 26863196 MeRIP-seq:(Medium) rs1295209247 Functional Loss SNV dbSNP153 33..33 33 - - - 80781 RMVar_ID_80781 Human_SNP_ID_656087106 m1A Human chr19 + 3401138 3401138 3401138 AGGAACAGTGAGGAGGCCTGTGTGGCTGCAGCAGAGTGAGGAGAGGAAGAGAAGGAGGAGGGGAG AGGAACAGTGAGGAGGCCTGTGTGGCTGCAGCGGAGTGAGGAGAGGAAGAGAAGGAGGAGGGGAG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3401135..3401206 26863196 MeRIP-seq:(Medium) rs1028218997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191068,Human_RBP_ID_17190850 RMVar_hsa_circ_268967,RMVar_hsa_circ_327862,RMVar_hsa_circ_353774,RMVar_hsa_circ_335847 80782 RMVar_ID_80782 Human_SNP_ID_656088078 m1A Human chr19 - 3404335 3404335 3404335 GCAAGGTTAAAAATACCCGCACGCACACCCTCACCCCCACCCCCTCCCGGTCCCGCCAATGTCAA GCAAGGTTAAAAATACCCGCACGCACACCCTCCCCCCCACCCCCTCCCGGTCCCGCCAATGTCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3404332..3404533;chr19:3404329..3404640 26863196 MeRIP-seq:(Medium) rs955085827 Functional Loss SNV dbSNP153 33..33 33 - - - 80783 RMVar_ID_80783 Human_SNP_ID_656089973 m1A Human chr19 - 3410403 3410403 3410403 CTGCCTGGAACACTGTTCCCTCAGCTATCTACATGGCTCATTCTCTCCCCTCATTCAGGACTTTC CTGCCTGGAACACTGTTCCCTCAGCTATCTACGTGGCTCATTCTCTCCCCTCATTCAGGACTTTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3410393..3410504 26863196 MeRIP-seq:(Medium) rs1369337432 Functional Loss SNV dbSNP153 33..33 33 - - - 80784 RMVar_ID_80784 Human_SNP_ID_656094523 m1A Human chr19 + 3426655 3426655 3426655 CCAGGTCCTCCCTGTGGCCCACAAGGCCCTGCACAACCTGTCCCATCCCTGCCCTGTCCTCCCCT CCAGGTCCTCCCTGTGGCCCACAAGGCCCTGCGCAACCTGTCCCATCCCTGCCCTGTCCTCCCCT A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3426652..3426717 26863196 MeRIP-seq:(Medium) rs1419804929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17081566 RMVar_hsa_circ_23597,RMVar_hsa_circ_268967,RMVar_hsa_circ_353774,RMVar_hsa_circ_335847,RMVar_hsa_circ_317934,RMVar_hsa_circ_331685,RMVar_hsa_circ_322152,RMVar_hsa_circ_270597,RMVar_hsa_circ_191338,RMVar_hsa_circ_191339,RMVar_hsa_circ_191337 80785 RMVar_ID_80785 Human_SNP_ID_656097283 m1A Human chr19 - 3435218 3435218 3435218 ACTCAGACCGGAAGGCCGGCTCCGCCCCCGCCACCAGCCCTACCTCCTTCCATGTCCTCCGTCCA ACTCAGACCGGAAGGCCGGCTCCGCCCCCGCCCCCAGCCCTACCTCCTTCCATGTCCTCCGTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3435214..3435312 26863196 MeRIP-seq:(Medium) rs1159951945 Functional Loss SNV dbSNP153 33..33 33 - - - 80786 RMVar_ID_80786 Human_SNP_ID_656100122 m1A Human chr19 + 3444136 3444136 3444136 AATACAAAGAGGAGGTCAGATGGGCGTGTGTGACAAATGGCTGCTCCGACGGGGTGATGAGGGCC AATACAAAGAGGAGGTCAGATGGGCGTGTGTGTCAAATGGCTGCTCCGACGGGGTGATGAGGGCC A T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3444133..3444317 26863196 MeRIP-seq:(Medium) rs1160345963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17920733 RMVar_hsa_circ_335847,RMVar_hsa_circ_317934,RMVar_hsa_circ_331685,RMVar_hsa_circ_322152,RMVar_hsa_circ_191338,RMVar_hsa_circ_191339,RMVar_hsa_circ_331629,RMVar_hsa_circ_368482 80787 RMVar_ID_80787 Human_SNP_ID_656100200 m1A Human chr19 - 3444379 3444379 3444379 TGGCCATCTTTCCTCTCAGGGAACACATCCATACGCCCCTCCCGGCATCCTGAATGCCCCATCTG TGGCCATCTTTCCTCTCAGGGAACACATCCATTCGCCCCTCCCGGCATCCTGAATGCCCCATCTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3444372..3444509 26863196 MeRIP-seq:(Medium) rs909113501 Functional Loss SNV dbSNP153 33..33 33 - - - 80788 RMVar_ID_80788 Human_SNP_ID_656101550 m1A Human chr19 + 3449080 3449080 3449080 CAAGTCACCATTCAACAGCCCGTCCCCCCAGGACTCTCCCCGCCTCTCCAGCTTCACCCAGCACC CAAGTCACCATTCAACAGCCCGTCCCCCCAGGCCTCTCCCCGCCTCTCCAGCTTCACCCAGCACC A C NFIC Ensembl:ENSG00000141905 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3449001..3449250 26863196 MeRIP-seq:(Medium) rs763335436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8483379,Human_RBP_ID_26335161,Human_RBP_ID_26814931,Human_RBP_ID_27473434 Human_Splice_Rec_1937192,Human_Splice_Rec_1937193,Human_Splice_Rec_1937212,Human_Splice_Rec_1937213,Human_Splice_Rec_1937232,Human_Splice_Rec_1937233,Human_Splice_Rec_1937248,Human_Splice_Rec_1937249,Human_Splice_Rec_1937264,Human_Splice_Rec_1937265,Human_Splice_Rec_1937280,Human_Splice_Rec_1937281,Human_Splice_Rec_1937298,Human_Splice_Rec_1937299,Human_Splice_Rec_1937310,Human_Splice_Rec_1937311 Human_miRNA_ID_135159,Human_miRNA_ID_254398,Human_miRNA_ID_427307,Human_miRNA_ID_1262237,Human_miRNA_ID_1339923,Human_miRNA_ID_2041334,Human_miRNA_ID_2147306,Human_miRNA_ID_2988733,Human_miRNA_ID_3020317,Human_miRNA_ID_3022432 RMVar_hsa_circ_335847,RMVar_hsa_circ_317934,RMVar_hsa_circ_331685,RMVar_hsa_circ_322152,RMVar_hsa_circ_191338,RMVar_hsa_circ_191339,RMVar_hsa_circ_331629,RMVar_hsa_circ_368482,RMVar_hsa_circ_191340,RMVar_hsa_circ_372879 80789 RMVar_ID_80789 Human_SNP_ID_656102586 m1A Human chr19 - 3452424 3452424 3452424 TTACTTGGGGGCTCCAGCCGGTCTGCTCTGTGACCGTGTGACTGTGTGTCTGTGGGTGTCATTCC TTACTTGGGGGCTCCAGCCGGTCTGCTCTGTGCCCGTGTGACTGTGTGTCTGTGGGTGTCATTCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3452417..3452675 26863196 MeRIP-seq:(Medium) rs11668557 Functional Loss SNV dbSNP153 33..33 33 - - - 80790 RMVar_ID_80790 Human_SNP_ID_656102670 m1A Human chr19 + 3452569 3452569 3452569 CCTACCCCAGACGGCCTCCACCTACTTCCCCCACACGGCCATCCGCTACCCACCTCATCTCAACC CCTACCCCAGACGGCCTCCACCTACTTCCCCCCCACGGCCATCCGCTACCCACCTCATCTCAACC A C NFIC Ensembl:ENSG00000141905 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:3449026..3452675;chr19:3452418..3452675 26863196 MeRIP-seq:(Medium) rs1172051069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8483381,Human_RBP_ID_17267848,Human_RBP_ID_17387130,Human_RBP_ID_18946249,Human_RBP_ID_26816605,Human_RBP_ID_27466920 Human_Splice_Rec_1937194,Human_Splice_Rec_1937195,Human_Splice_Rec_1937214,Human_Splice_Rec_1937215,Human_Splice_Rec_1937234,Human_Splice_Rec_1937235,Human_Splice_Rec_1937250,Human_Splice_Rec_1937251,Human_Splice_Rec_1937266,Human_Splice_Rec_1937267,Human_Splice_Rec_1937282,Human_Splice_Rec_1937283,Human_Splice_Rec_1937300,Human_Splice_Rec_1937301,Human_Splice_Rec_1937312,Human_Splice_Rec_1937313,Human_Splice_Rec_1937315,Human_Splice_Rec_1937321 Human_miRNA_ID_2946308 RMVar_hsa_circ_317934,RMVar_hsa_circ_331685,RMVar_hsa_circ_191339,RMVar_hsa_circ_368482,RMVar_hsa_circ_191340,RMVar_hsa_circ_372879 80791 RMVar_ID_80791 Human_SNP_ID_656103139 m1A Human chr19 - 3453883 3453883 3453883 AGGCGAGGTCGGCGACGTGGCTCCTCCCTCGGAGGTGGTGGCGGGTTTGGTGGCAGGGGGGAGCG AGGCGAGGTCGGCGACGTGGCTCCTCCCTCGGGGGTGGTGGCGGGTTTGGTGGCAGGGGGGAGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3453833..3453955 26863196 MeRIP-seq:(Medium) rs76933523 Functional Loss SNV dbSNP153 33..33 33 - - - 80792 RMVar_ID_80792 Human_SNP_ID_656104598 m1A Human chr19 - 3458529 3458529 3458529 ATGCTGAGAAAGGTGCCACCCTTGCCTGCCTCAGTTTCCCTTCCCTCCCAGGCTTGGGTGGGGTG ATGCTGAGAAAGGTGCCACCCTTGCCTGCCTCGGTTTCCCTTCCCTCCCAGGCTTGGGTGGGGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3458527..3459003 26863196 MeRIP-seq:(Medium) rs1049483320 Functional Loss SNV dbSNP153 33..33 33 - - - 80793 RMVar_ID_80793 Human_SNP_ID_656105880 m1A Human chr19 + 3462963 3462957 3462963 CTCAGGAGGAAAAGAAAAAACAAAGGCAGAAGAAGAAGAAGAAGAAATAAAAACCCACCCAAGCA CTCAGGAGGAAAAGAAAAAACAAAGGC______AGAAGAAGAAGAAATAAAAACCCACCCAAGCA CAGAAGA C NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:3462948..3463142;chr19:3462951..3463000 26863196 MeRIP-seq:(Medium) rs926546201 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_55407,Human_RBP_ID_27466927 80794 RMVar_ID_80794 Human_SNP_ID_656105881 m1A Human chr19 + 3462963 3462957 3462963 CTCAGGAGGAAAAGAAAAAACAAAGGCAGAAGAAGAAGAAGAAGAAATAAAAACCCACCCAAGCA CTCAGGAGGAAAAGAAAAAACAAAGGCAGA___AGAAGAAGAAGAAATAAAAACCCACCCAAGCA CAGAAGA CAGA NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:3462948..3463142;chr19:3462951..3463000 26863196 MeRIP-seq:(Medium) rs926546201 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_55407,Human_RBP_ID_27466927 80795 RMVar_ID_80795 Human_SNP_ID_656106251 m1A Human chr19 - 3463900 3463897 3463900 GGCTGGTGGAGAGGCTGGAGGGGAGGGGGAGGAGGCCCGCGGCCATTCCGTGTCCCAGCTGGACA GGCTGGTGGAGAGGCTGGAGGGGAGGGGGAGG___CCCGCGGCCATTCCGTGTCCCAGCTGGACA GCCT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3463893..3464817 26863196 MeRIP-seq:(Medium) rs1054861777 Functional Loss DEL dbSNP153 33..35 33 - - - 80796 RMVar_ID_80796 Human_SNP_ID_656106252 m1A Human chr19 - 3463900 3463900 3463900 GGCTGGTGGAGAGGCTGGAGGGGAGGGGGAGGAGGCCCGCGGCCATTCCGTGTCCCAGCTGGACA GGCTGGTGGAGAGGCTGGAGGGGAGGGGGAGGGGGCCCGCGGCCATTCCGTGTCCCAGCTGGACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3463893..3464817 26863196 MeRIP-seq:(Medium) rs1292497329 Functional Loss SNV dbSNP153 33..33 33 - - - 80797 RMVar_ID_80797 Human_SNP_ID_656106354 m1A Human chr19 - 3464169 3464169 3464169 TCCCGCAGCTGGGCCCCGCGTCGGGGTAGGCGATGAAAGTGCAAACGGCGGTCCCCCTTCGCTGG TCCCGCAGCTGGGCCCCGCGTCGGGGTAGGCGTTGAAAGTGCAAACGGCGGTCCCCCTTCGCTGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3463876..3464901 26863196 MeRIP-seq:(Medium) rs552206999 Functional Loss SNV dbSNP153 33..33 33 - - - 80798 RMVar_ID_80798 Human_SNP_ID_656106545 m1A Human chr19 + 3464649 3464649 3464649 CAGGTCTCCGGGTCTCACCTGCTCCTAGCCTCACCCCCCTGCCCCCGAAAACCAGACTCTCCTCC CAGGTCTCCGGGTCTCACCTGCTCCTAGCCTCCCCCCCCTGCCCCCGAAAACCAGACTCTCCTCC A C NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3464548..3464848 26863196 MeRIP-seq:(Medium) rs551936001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55415,Human_RBP_ID_140220,Human_RBP_ID_5130880,Human_RBP_ID_18944784,Human_RBP_ID_22969513 80799 RMVar_ID_80799 Human_SNP_ID_656106589 m1A Human chr19 - 3464777 3464777 3464777 CAGACGGACGGAGGGACCAAGGGCTCGAGGCCAGAGGATGGCGAACCTCTCTTGGGGGTGATGGG CAGACGGACGGAGGGACCAAGGGCTCGAGGCCTGAGGATGGCGAACCTCTCTTGGGGGTGATGGG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3464526..3464925 26863196 MeRIP-seq:(Medium) rs1025434694 Functional Loss SNV dbSNP153 33..33 33 - - - 80800 RMVar_ID_80800 Human_SNP_ID_656106653 m1A Human chr19 + 3464998 3464998 3464998 CCGGGCTCCAGAGGGGTCAGGGCGCGACGAGAACCAACTCTTTACCTAACTTTGCATGGTGCTTA CCGGGCTCCAGAGGGGTCAGGGCGCGACGAGAGCCAACTCTTTACCTAACTTTGCATGGTGCTTA A G NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3464947..3465094 26863196 MeRIP-seq:(Medium) rs556315570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1014779,Human_RBP_ID_3580421,Human_RBP_ID_5319990,Human_RBP_ID_6742467,Human_RBP_ID_8096618,Human_RBP_ID_9291810,Human_RBP_ID_17920761,Human_RBP_ID_18165531,Human_RBP_ID_18303400,Human_RBP_ID_18461702,Human_RBP_ID_18489630,Human_RBP_ID_22593023,Human_RBP_ID_26335164,Human_RBP_ID_26783566,Human_RBP_ID_27466960 80801 RMVar_ID_80801 Human_SNP_ID_656106675 m1A Human chr19 + 3465093 3465093 3465093 GTCAGCTGGCGGCGCTGACACACATGCATGGCAGACTATCCCTGGCTCTATCTCCCTGTTCCTCG GTCAGCTGGCGGCGCTGACACACATGCATGGCCGACTATCCCTGGCTCTATCTCCCTGTTCCTCG A C NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3464942..3465188 26863196 MeRIP-seq:(Medium) rs555454470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27466966 Human_miRNA_ID_1009334 80802 RMVar_ID_80802 Human_SNP_ID_656106864 m1A Human chr19 + 3465553 3465553 3465553 GCTGTCCTTGGTCCTGTCTCCCCTCCTGCTGTATTCAGGGGTGCCCCCTGGTGCTCAGCCTCTAC GCTGTCCTTGGTCCTGTCTCCCCTCCTGCTGTTTTCAGGGGTGCCCCCTGGTGCTCAGCCTCTAC A T NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3465526..3465575 26863196 MeRIP-seq:(Medium) rs572597868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2563109,Human_RBP_ID_4518909,Human_RBP_ID_5321135,Human_RBP_ID_17082195 Human_miRNA_ID_960230 80803 RMVar_ID_80803 Human_SNP_ID_656106865 m1A Human chr19 + 3465557 3465556 3465557 TCCTTGGTCCTGTCTCCCCTCCTGCTGTATTCAGGGGTGCCCCCTGGTGCTCAGCCTCTACCACC TCCTTGGTCCTGTCTCCCCTCCTGCTGTATTC_GGGGTGCCCCCTGGTGCTCAGCCTCTACCACC CA C NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3465510..3465582 26863196 MeRIP-seq:(Medium) rs1364994042 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2563109,Human_RBP_ID_17082195 Human_miRNA_ID_960230 80804 RMVar_ID_80804 Human_SNP_ID_656107449 m1A Human chr19 + 3467656 3467656 3467656 CCACTGTCCCTTGCAAGACAGGTTCTGGAGCCAGGAGCAACTGTCCAGCCCTCCAGAAGAGACAG CCACTGTCCCTTGCAAGACAGGTTCTGGAGCCGGGAGCAACTGTCCAGCCCTCCAGAAGAGACAG A G NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3467607..3467699 26863196 MeRIP-seq:(Medium) rs1422938002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139175,Human_RBP_ID_20349251 Human_miRNA_ID_254404,Human_miRNA_ID_794310 80805 RMVar_ID_80805 Human_SNP_ID_656114218 m1A Human chr19 - 3491200 3491200 3491200 GAGGCTCTGGGATGCCCGGCTCAGGACAGGGGAGGATTGCGAGGGAAGCCAGGGGAGGATCGCGA GAGGCTCTGGGATGCCCGGCTCAGGACAGGGGCGGATTGCGAGGGAAGCCAGGGGAGGATCGCGA T G DOHH Ensembl:ENSG00000129932 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:3491151..3491416;chr19:3491151..3491813;chr19:3491151..3491763;chr19:3491151..3491725 26863196 MeRIP-seq:(Medium) rs1303650917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825439,Human_RBP_ID_1014846,Human_RBP_ID_6744685,Human_RBP_ID_8195684 RMVar_hsa_circ_83227,RMVar_hsa_circ_191345 80806 RMVar_ID_80806 Human_SNP_ID_656114718 m1A Human chr19 + 3492346 3492346 3492346 CATGGCGCGGTATCGCTCGAAGAGCGGCCGGGACTCATCCAGCAGCGCCTCCCGCAGGCGCCCCA CATGGCGCGGTATCGCTCGAAGAGCGGCCGGGTCTCATCCAGCAGCGCCTCCCGCAGGCGCCCCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3492295..3492436 26863196 MeRIP-seq:(Medium) rs777073505 Functional Loss SNV dbSNP153 33..33 33 - - - 80807 RMVar_ID_80807 Human_SNP_ID_656116130 m1A Human chr19 - 3496822 3496822 3496822 TGAGCAGGGTTGTGGAAGGCCGGGACCCATTGACAGCACGATGGTGACGGAGCAGGAGGTGGATG TGAGCAGGGTTGTGGAAGGCCGGGACCCATTGGCAGCACGATGGTGACGGAGCAGGAGGTGGATG T C DOHH Ensembl:ENSG00000129932 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:3496551..3496914;chr19:3496576..3496921;chr19:3496702..3496930 26863196 MeRIP-seq:(Medium) rs767998437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557900,Human_RBP_ID_6745500,Human_RBP_ID_17921132,Human_RBP_ID_22233720 Human_Splice_Rec_1937340,Human_Splice_Rec_1937348 RMVar_hsa_circ_191346,RMVar_hsa_circ_311826 80808 RMVar_ID_80808 Human_SNP_ID_656118777 m1A Human chr19 + 3506296 3506296 3506296 CGCGCGGCCGGCCGGGCGCGCGCGGCGGAGGGAGGGAGCCGGGAGGCAGCGGAGGAGCGACCGCC CGCGCGGCCGGCCGGGCGCGCGCGGCGGAGGGGGGGAGCCGGGAGGCAGCGGAGGAGCGACCGCC A G FZR1 Ensembl:ENSG00000105325 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3506293..3506476 26863196 MeRIP-seq:(Medium) rs1307490546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4519907,Human_RBP_ID_18421188 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867 80809 RMVar_ID_80809 Human_SNP_ID_656118830 m1A Human chr19 + 3506432 3506432 3506432 GGCCGGAGGCGGGCGCTGTGCGGTGCCAGGAGAGGCGGGGTCGGCGGGAGCCAGCGAGCCACGGG GGCCGGAGGCGGGCGCTGTGCGGTGCCAGGAGGGGCGGGGTCGGCGGGAGCCAGCGAGCCACGGG A G FZR1 Ensembl:ENSG00000105325 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3506348..3506437 26863410 MeRIP-seq:(Medium) rs1258516937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910193,Human_RBP_ID_4557087,Human_RBP_ID_8942144,Human_RBP_ID_18192716,Human_RBP_ID_18421188,Human_RBP_ID_27815807 Human_Splice_Rec_1937363,Human_Splice_Rec_1937389,Human_Splice_Rec_1937419 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867 80810 RMVar_ID_80810 Human_SNP_ID_656119149 m1A Human chr19 - 3507281 3507281 3507281 ATCCGAGATGGCCAGGCTTGCGTTTGGAGAAGACACGGGGCAGGACGCAGGACGGAGGTTCAGTT ATCCGAGATGGCCAGGCTTGCGTTTGGAGAAGTCACGGGGCAGGACGCAGGACGGAGGTTCAGTT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3507071..3507508 26863196 MeRIP-seq:(Medium) rs551816579 Functional Loss SNV dbSNP153 33..33 33 - - - 80811 RMVar_ID_80811 Human_SNP_ID_656119150 m1A Human chr19 - 3507281 3507281 3507281 ATCCGAGATGGCCAGGCTTGCGTTTGGAGAAGACACGGGGCAGGACGCAGGACGGAGGTTCAGTT ATCCGAGATGGCCAGGCTTGCGTTTGGAGAAGGCACGGGGCAGGACGCAGGACGGAGGTTCAGTT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3507071..3507508 26863196 MeRIP-seq:(Medium) rs551816579 Functional Loss SNV dbSNP153 33..33 33 - - - 80812 RMVar_ID_80812 Human_SNP_ID_656123580 m1A Human chr19 + 3523003 3523003 3523003 GGCCGAGCCCTGCCTCGCCATGGACCAGGACTATGAGCGGCGCCTGCTTCGCCAGATCGTCATCC GGCCGAGCCCTGCCTCGCCATGGACCAGGACTTTGAGCGGCGCCTGCTTCGCCAGATCGTCATCC A T FZR1 Ensembl:ENSG00000105325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3522905..3523123 26863196 MeRIP-seq:(Medium) rs771143636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910194,Human_RBP_ID_3568535,Human_RBP_ID_4557903,Human_RBP_ID_13434946,Human_RBP_ID_18728754 Human_Splice_Rec_1937364,Human_Splice_Rec_1937365,Human_Splice_Rec_1937394,Human_Splice_Rec_1937395,Human_Splice_Rec_1937420,Human_Splice_Rec_1937421,Human_Splice_Rec_1937427,Human_Splice_Rec_1937451,Human_Splice_Rec_1937475 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867 80813 RMVar_ID_80813 Human_SNP_ID_656123700 m1A Human chr19 + 3523438 3523410 3523438 GGGGGCCCTGGCTTTGTCCTTCCTTGCGCTCCACCCTGCCTCCCCAGCCCAGCCGTGTTTGCCTT GGGGG____________________________CCCTGCCTCCCCAGCCCAGCCGTGTTTGCCTT GCCCTGGCTTTGTCCTTCCTTGCGCTCCA G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3523401..3523600 26863196 MeRIP-seq:(Medium) rs1381581801 Functional Loss DEL dbSNP153 6..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867 80814 RMVar_ID_80814 Human_SNP_ID_656123713 m1A Human chr19 + 3523438 3523438 3523438 GGGGGCCCTGGCTTTGTCCTTCCTTGCGCTCCACCCTGCCTCCCCAGCCCAGCCGTGTTTGCCTT GGGGGCCCTGGCTTTGTCCTTCCTTGCGCTCCTCCCTGCCTCCCCAGCCCAGCCGTGTTTGCCTT A T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3523401..3523600 26863196 MeRIP-seq:(Medium) rs12977788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867 80815 RMVar_ID_80815 Human_SNP_ID_656124686 m1A Human chr19 - 3526208 3526208 3526208 GTGAGGCGGGGCAAGGCAGGGTGGGGGCCTGCAGGGCGGATGGGCTGGGACCCTAACCTTTGCCG GTGAGGCGGGGCAAGGCAGGGTGGGGGCCTGCGGGGCGGATGGGCTGGGACCCTAACCTTTGCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3526202..3526322 26863196 MeRIP-seq:(Medium) rs770734196 Functional Loss SNV dbSNP153 33..33 33 - - - 80816 RMVar_ID_80816 Human_SNP_ID_656124687 m1A Human chr19 - 3526208 3526208 3526208 GTGAGGCGGGGCAAGGCAGGGTGGGGGCCTGCAGGGCGGATGGGCTGGGACCCTAACCTTTGCCG GTGAGGCGGGGCAAGGCAGGGTGGGGGCCTGCCGGGCGGATGGGCTGGGACCCTAACCTTTGCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3526202..3526322 26863196 MeRIP-seq:(Medium) rs770734196 Functional Loss SNV dbSNP153 33..33 33 - - - 80817 RMVar_ID_80817 Human_SNP_ID_656125019 m1A Human chr19 + 3527014 3527014 3527014 TTCCCTTAGCACCAAGCGCTCCAGCCCCGATGACGGCAACGATGTGTCTCCCTACTCCCTGTCTC TTCCCTTAGCACCAAGCGCTCCAGCCCCGATGGCGGCAACGATGTGTCTCCCTACTCCCTGTCTC A G FZR1 Ensembl:ENSG00000105325 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3527012..3527275 26863196 MeRIP-seq:(Medium) rs972459532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22970300 Human_Splice_Rec_1937372,Human_Splice_Rec_1937373,Human_Splice_Rec_1937402,Human_Splice_Rec_1937403,Human_Splice_Rec_1937426,Human_Splice_Rec_1937434,Human_Splice_Rec_1937435,Human_Splice_Rec_1937458,Human_Splice_Rec_1937459,Human_Splice_Rec_1937498,Human_Splice_Rec_1937499 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_338218,RMVar_hsa_circ_364580,RMVar_hsa_circ_191348,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_107166,RMVar_hsa_circ_191350,RMVar_hsa_circ_191351,RMVar_hsa_circ_88251,RMVar_hsa_circ_191352 80818 RMVar_ID_80818 Human_SNP_ID_656125025 m1A Human chr19 - 3527030 3527030 3527030 CTCTTGTTGCTGACGGGAGACAGGGAGTAGGGAGACACATCGTTGCCGTCATCGGGGCTGGAGCG CTCTTGTTGCTGACGGGAGACAGGGAGTAGGGGGACACATCGTTGCCGTCATCGGGGCTGGAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3526944..3527097 26863196 MeRIP-seq:(Medium) rs529806846 Functional Loss SNV dbSNP153 33..33 33 - - - 80819 RMVar_ID_80819 Human_SNP_ID_656125196 m1A Human chr19 + 3527590 3527590 3527590 GACACTTCCCAAGCGTTTGCAAGAGGTGACCCAAGTGCCGTGGCTCACGGATGCCACGTGGCCGC GACACTTCCCAAGCGTTTGCAAGAGGTGACCCTAGTGCCGTGGCTCACGGATGCCACGTGGCCGC A T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3527581..3527661 26863196 MeRIP-seq:(Medium) rs1306493050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5372813,Human_RBP_ID_19088654 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80820 RMVar_ID_80820 Human_SNP_ID_656125787 m1A Human chr19 - 3528961 3528961 3528961 ATCCATCCGCTCAACCATCTGCTCTCCCATCCACTCACCCATCCGCTCTCCCATCCACTCCCATA ATCCATCCGCTCAACCATCTGCTCTCCCATCCGCTCACCCATCCGCTCTCCCATCCACTCCCATA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3528952..3529370 26863196 MeRIP-seq:(Medium) rs1454689680 Functional Loss SNV dbSNP153 33..33 33 - - - 80821 RMVar_ID_80821 Human_SNP_ID_656125788 m1A Human chr19 - 3528961 3528961 3528961 ATCCATCCGCTCAACCATCTGCTCTCCCATCCACTCACCCATCCGCTCTCCCATCCACTCCCATA ATCCATCCGCTCAACCATCTGCTCTCCCATCCCCTCACCCATCCGCTCTCCCATCCACTCCCATA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3528952..3529370 26863196 MeRIP-seq:(Medium) rs1454689680 Functional Loss SNV dbSNP153 33..33 33 - - - 80822 RMVar_ID_80822 Human_SNP_ID_656125988 m1A Human chr19 + 3529205 3529203 3529205 AGCGGTTGGGAGAGCGGATGGGAGAGCGGATGAGAGAGTGGATGGTTGAGCGGATGGGAGAGCGG AGCGGTTGGGAGAGCGGATGGGAGAGCGGAT__GAGAGTGGATGGTTGAGCGGATGGGAGAGCGG TGA T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529201..3529385 26863196 MeRIP-seq:(Medium) rs1459221358 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5649709 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80823 RMVar_ID_80823 Human_SNP_ID_656125989 m1A Human chr19 + 3529205 3529205 3529205 AGCGGTTGGGAGAGCGGATGGGAGAGCGGATGAGAGAGTGGATGGTTGAGCGGATGGGAGAGCGG AGCGGTTGGGAGAGCGGATGGGAGAGCGGATGGGAGAGTGGATGGTTGAGCGGATGGGAGAGCGG A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529201..3529385 26863196 MeRIP-seq:(Medium) rs1239127027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5649709 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80824 RMVar_ID_80824 Human_SNP_ID_656126103 m1A Human chr19 + 3529405 3529393 3529405 CAGATGGGAGAGCAGATGGGTGAGCGGATGGGAGAGCAGATGGGAGAGTGGATGAGAGTGGTTGA CAGATGGGAGAGCAGATGGGT____________GAGCAGATGGGAGAGTGGATGAGAGTGGTTGA TGAGCGGATGGGA T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529401..3529425 26863196 MeRIP-seq:(Medium) rs1396186873 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80825 RMVar_ID_80825 Human_SNP_ID_656126110 m1A Human chr19 + 3529405 3529405 3529405 CAGATGGGAGAGCAGATGGGTGAGCGGATGGGAGAGCAGATGGGAGAGTGGATGAGAGTGGTTGA CAGATGGGAGAGCAGATGGGTGAGCGGATGGGTGAGCAGATGGGAGAGTGGATGAGAGTGGTTGA A T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529401..3529425 26863196 MeRIP-seq:(Medium) rs1441636000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80826 RMVar_ID_80826 Human_SNP_ID_656126136 m1A Human chr19 + 3529463 3529463 3529463 TGGTTGAGGGAGTGGCTGGTTGAGTGGATGGGAGAGCAGATGGGAGAGCAGATGGGAGAGCAGAT TGGTTGAGGGAGTGGCTGGTTGAGTGGATGGGGGAGCAGATGGGAGAGCAGATGGGAGAGCAGAT A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529451..3529525 26863196 MeRIP-seq:(Medium) rs1288208673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80827 RMVar_ID_80827 Human_SNP_ID_656126140 m1A Human chr19 + 3529470 3529470 3529470 GGGAGTGGCTGGTTGAGTGGATGGGAGAGCAGATGGGAGAGCAGATGGGAGAGCAGATGGGTGAG GGGAGTGGCTGGTTGAGTGGATGGGAGAGCAGGTGGGAGAGCAGATGGGAGAGCAGATGGGTGAG A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3528688..3529493 26863196 MeRIP-seq:(Medium) rs528969586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5292921 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80828 RMVar_ID_80828 Human_SNP_ID_656126190 m1A Human chr19 - 3529607 3529607 3529607 ACCCATCCGCTCTCCCATCTGCTCAACCATCCACTCCCTCAACCACTCTCATCCACTCACCCATC ACCCATCCGCTCTCCCATCTGCTCAACCATCCTCTCCCTCAACCACTCTCATCCACTCACCCATC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3529558..3529795 26863196 MeRIP-seq:(Medium) rs1219272112 Functional Loss SNV dbSNP153 33..33 33 - - - 80829 RMVar_ID_80829 Human_SNP_ID_656126191 m1A Human chr19 - 3529607 3529607 3529607 ACCCATCCGCTCTCCCATCTGCTCAACCATCCACTCCCTCAACCACTCTCATCCACTCACCCATC ACCCATCCGCTCTCCCATCTGCTCAACCATCCGCTCCCTCAACCACTCTCATCCACTCACCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3529558..3529795 26863196 MeRIP-seq:(Medium) rs1219272112 Functional Loss SNV dbSNP153 33..33 33 - - - 80830 RMVar_ID_80830 Human_SNP_ID_656126193 m1A Human chr19 - 3529614 3529614 3529614 TCTGCTCACCCATCCGCTCTCCCATCTGCTCAACCATCCACTCCCTCAACCACTCTCATCCACTC TCTGCTCACCCATCCGCTCTCCCATCTGCTCACCCATCCACTCCCTCAACCACTCTCATCCACTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr19:3529607..3529788;chr19:3529601..3529800 26863196 MeRIP-seq:(Medium) rs1235727975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8484117 80831 RMVar_ID_80831 Human_SNP_ID_656126256 m1A Human chr19 + 3529709 3529697 3529709 TGGTTGAGGGAGTGGATGGTTGAGCGGATGGGAGAGCGGATGGGAGAGTGGATGGGAGAGTGGAT TGGTTGAGGGAGTGGATGGTT____________GAGCGGATGGGAGAGTGGATGGGAGAGTGGAT TGAGCGGATGGGA T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529701..3529725 26863196 MeRIP-seq:(Medium) rs1187922209 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5292613,Human_RBP_ID_5649712,Human_RBP_ID_23793145 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80832 RMVar_ID_80832 Human_SNP_ID_656126272 m1A Human chr19 + 3529709 3529709 3529709 TGGTTGAGGGAGTGGATGGTTGAGCGGATGGGAGAGCGGATGGGAGAGTGGATGGGAGAGTGGAT TGGTTGAGGGAGTGGATGGTTGAGCGGATGGGTGAGCGGATGGGAGAGTGGATGGGAGAGTGGAT A T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529701..3529725 26863196 MeRIP-seq:(Medium) rs1441541824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5292613,Human_RBP_ID_5649712,Human_RBP_ID_23793145 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80833 RMVar_ID_80833 Human_SNP_ID_656126315 m1A Human chr19 + 3529762 3529760 3529762 GGGAGAGTGGATGGGTGAGCGCATGGGAGCGCATGGGTGAGCGGATGCGAGAGTGGATGAGAGTG GGGAGAGTGGATGGGTGAGCGCATGGGAGCG__TGGGTGAGCGGATGCGAGAGTGGATGAGAGTG GCA G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3529726..3529800 26863196 MeRIP-seq:(Medium) rs1258209269 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5292613,Human_RBP_ID_5649712,Human_RBP_ID_23793146 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80834 RMVar_ID_80834 Human_SNP_ID_656126318 m1A Human chr19 + 3529762 3529762 3529762 GGGAGAGTGGATGGGTGAGCGCATGGGAGCGCATGGGTGAGCGGATGCGAGAGTGGATGAGAGTG GGGAGAGTGGATGGGTGAGCGCATGGGAGCGCGTGGGTGAGCGGATGCGAGAGTGGATGAGAGTG A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3529726..3529800 26863196 MeRIP-seq:(Medium) rs558772891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5292613,Human_RBP_ID_5649712,Human_RBP_ID_23793146 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80835 RMVar_ID_80835 Human_SNP_ID_656126514 m1A Human chr19 - 3530019 3530019 3530019 TCCCATCCGCTCACCCATCCACTCTCCCATCCACTCACCCATCTGCTCTCCCATCCACTCAACCA TCCCATCCGCTCACCCATCCACTCTCCCATCCGCTCACCCATCTGCTCTCCCATCCACTCAACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3529975..3530122 26863196 MeRIP-seq:(Medium) rs1447350856 Functional Loss SNV dbSNP153 33..33 33 - - - 80836 RMVar_ID_80836 Human_SNP_ID_656126616 m1A Human chr19 + 3530208 3530196 3530208 GAGGGAGTGGATGGTTGAGCGGATGGGAGAGCAGATGGGAGAGTGGATGGGTGAGCGGATGGGAG GAGGGAGTGGATGGTTGAGCG____________GATGGGAGAGTGGATGGGTGAGCGGATGGGAG GGATGGGAGAGCA G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3530173..3530758 26863196 MeRIP-seq:(Medium) rs1157559197 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80837 RMVar_ID_80837 Human_SNP_ID_656126623 m1A Human chr19 + 3530208 3530208 3530208 GAGGGAGTGGATGGTTGAGCGGATGGGAGAGCAGATGGGAGAGTGGATGGGTGAGCGGATGGGAG GAGGGAGTGGATGGTTGAGCGGATGGGAGAGCGGATGGGAGAGTGGATGGGTGAGCGGATGGGAG A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3530173..3530758 26863196 MeRIP-seq:(Medium) rs1226102568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80838 RMVar_ID_80838 Human_SNP_ID_656126668 m1A Human chr19 + 3530277 3530267 3530277 GATGGGTGAGCGGATGGGAGAGCGGATGGGAGAGCGGATGGGAGAGCGCAGGGGAGAGCGGAGGA GATGGGTGAGCGGATGGGAGAGC__________GCGGATGGGAGAGCGCAGGGGAGAGCGGAGGA CGGATGGGAGA C FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3530261..3530523 26863196 MeRIP-seq:(Medium) rs1207911269 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5649713 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80839 RMVar_ID_80839 Human_SNP_ID_656126733 m1A Human chr19 - 3530365 3530353 3530365 GCTCACCCATCTGCTCACCCATCCGCTCTCCCATCCGCTCTCCCTTCTGCTCAACCATCCACTCC GCTCACCCATCTGCTCACCCATCCGCTCTCCC____________TTCTGCTCAACCATCCACTCC AGGGAGAGCGGAT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3529976..3530900 26863196 MeRIP-seq:(Medium) rs1186681159 Functional Loss DEL dbSNP153 33..44 33 - - - 80840 RMVar_ID_80840 Human_SNP_ID_656126740 m1A Human chr19 - 3530365 3530365 3530365 GCTCACCCATCTGCTCACCCATCCGCTCTCCCATCCGCTCTCCCTTCTGCTCAACCATCCACTCC GCTCACCCATCTGCTCACCCATCCGCTCTCCCTTCCGCTCTCCCTTCTGCTCAACCATCCACTCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3529976..3530900 26863196 MeRIP-seq:(Medium) rs184548955 Functional Loss SNV dbSNP153 33..33 33 - - - 80841 RMVar_ID_80841 Human_SNP_ID_656126836 m1A Human chr19 + 3530477 3530465 3530477 CGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT CGCATGGGAGAGCGCATGGAT____________GAGCGCATGGGTGAGCGGATGCAAGAGTGGAT TGAGCGCATGGGA T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3529926..3530743 26863196 MeRIP-seq:(Medium) rs970472498 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80842 RMVar_ID_80842 Human_SNP_ID_656126846 m1A Human chr19 + 3530477 3530475 3530477 CGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT CGCATGGGAGAGCGCATGGATGAGCGCATGG__GAGCGCATGGGTGAGCGGATGCAAGAGTGGAT GGA G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3529926..3530743 26863196 MeRIP-seq:(Medium) rs200953287 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80843 RMVar_ID_80843 Human_SNP_ID_656126850 m1A Human chr19 + 3530477 3530477 3530477 CGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT CGCATGGGAGAGCGCATGGATGAGCGCATGGGGGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3529926..3530743 26863196 MeRIP-seq:(Medium) rs1309256391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80844 RMVar_ID_80844 Human_SNP_ID_656126851 m1A Human chr19 + 3530477 3530477 3530477 CGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT CGCATGGGAGAGCGCATGGATGAGCGCATGGGTGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT A T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3529926..3530743 26863196 MeRIP-seq:(Medium) rs1309256391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 80845 RMVar_ID_80845 Human_SNP_ID_656127596 m1A Human chr19 - 3532591 3532591 3532591 CAGATTGCACACTTGGGAGCCCGTGTCGATACACTGCAGTGGTTGTCCTGTCAGCGTGTTCCAGA CAGATTGCACACTTGGGAGCCCGTGTCGATACGCTGCAGTGGTTGTCCTGTCAGCGTGTTCCAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3531996..3533655 32194978 MeRIP-seq:(Medium) rs11542322 Functional Loss SNV dbSNP153 33..33 33 - - - 80846 RMVar_ID_80846 Human_SNP_ID_656128703 m1A Human chr19 + 3535848 3535848 3535848 CCAGCGCCAACAGCCGTGGGGAAGCCAAGGAGACCCAAGGGGTCCAGGAGGTGGGCGCCCTCCAT CCAGCGCCAACAGCCGTGGGGAAGCCAAGGAGCCCCAAGGGGTCCAGGAGGTGGGCGCCCTCCAT A C FZR1 Ensembl:ENSG00000105325 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3535800..3536049 32194978 MeRIP-seq:(Medium) rs1277972976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8484136,Human_RBP_ID_26473266 80847 RMVar_ID_80847 Human_SNP_ID_656129187 m1A Human chr19 + 3537150 3537150 3537150 AAGGGGGGTGAAGGCCGTGGTGGGAGGGTCCCATGATGATGGGCCAGGGCTCGTGTAGAAATGGG AAGGGGGGTGAAGGCCGTGGTGGGAGGGTCCCGTGATGATGGGCCAGGGCTCGTGTAGAAATGGG A G FZR1 Ensembl:ENSG00000105325 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3537026..3537450 26863196 MeRIP-seq:(Medium) rs990874084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3587562,Human_RBP_ID_17921258,Human_RBP_ID_18728809 80848 RMVar_ID_80848 Human_SNP_ID_656129434 m1A Human chr19 + 3537840 3537832 3537840 ACACAGCCCAGAGACAGAGAAGCTTATGAGGAAGTGAGGAGGTGGCGTCACAAGGGTGGGGAGGG ACACAGCCCAGAGACAGAGAAGCTT________GTGAGGAGGTGGCGTCACAAGGGTGGGGAGGG TATGAGGAA T FZR1 Ensembl:ENSG00000105325 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3537826..3537875 26863196 MeRIP-seq:(Medium) rs1027342033 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_17921260 80849 RMVar_ID_80849 Human_SNP_ID_656129488 m1A Human chr19 - 3537992 3537992 3537992 TTCCTCCCGCATACCAGGTGCCGTCCTGCCCCAGGGCCTTTGCATGGCTGTGCCCTTTGCCTCTC TTCCTCCCGCATACCAGGTGCCGTCCTGCCCCGGGGCCTTTGCATGGCTGTGCCCTTTGCCTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3537985..3538085 26863196 MeRIP-seq:(Medium) rs1225249231 Functional Loss SNV dbSNP153 33..33 33 - - - 80850 RMVar_ID_80850 Human_SNP_ID_656129663 m1A Human chr19 - 3538485 3538483 3538485 GAAATGTCCAGGACAGACCAATCCACAGAATCAGGGAGAGGATTCGTGGGTGCCGGGACTGGGGA GAAATGTCCAGGACAGACCAATCCACAGAATC__GGAGAGGATTCGTGGGTGCCGGGACTGGGGA CCT C MFSD12 Ensembl:ENSG00000161091 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3538476..3538525 26863196 MeRIP-seq:(Medium) rs1429896994 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_55458,Human_RBP_ID_519787,Human_RBP_ID_26335169 Human_miRNA_ID_120325,Human_miRNA_ID_124140 80851 RMVar_ID_80851 Human_SNP_ID_656129666 m1A Human chr19 - 3538485 3538485 3538485 GAAATGTCCAGGACAGACCAATCCACAGAATCAGGGAGAGGATTCGTGGGTGCCGGGACTGGGGA GAAATGTCCAGGACAGACCAATCCACAGAATCGGGGAGAGGATTCGTGGGTGCCGGGACTGGGGA T C MFSD12 Ensembl:ENSG00000161091 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3538476..3538525 26863196 MeRIP-seq:(Medium) rs1343320438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55458,Human_RBP_ID_519787,Human_RBP_ID_26335169 Human_miRNA_ID_120325,Human_miRNA_ID_124140 80852 RMVar_ID_80852 Human_SNP_ID_656129754 m1A Human chr19 - 3538666 3538666 3538666 AACACCGAACACCCAGTGAAGGTGAGGGGATCAGCACGGCGCCGCCACCGTGCTGGAACGAGACT AACACCGAACACCCAGTGAAGGTGAGGGGATCCGCACGGCGCCGCCACCGTGCTGGAACGAGACT T G MFSD12 Ensembl:ENSG00000161091 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3538616..3539100 26863196 MeRIP-seq:(Medium) rs944326539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519789 Human_Splice_Rec_1937516,Human_Splice_Rec_1937524,Human_Splice_Rec_1937526 80853 RMVar_ID_80853 Human_SNP_ID_656129812 m1A Human chr19 - 3538766 3538766 3538766 CCTCACCCACTCACATCCAGTCCGTTTGTAAAATACACCCAGGATGAGACCTGCACGCAGTGGCT CCTCACCCACTCACATCCAGTCCGTTTGTAAAGTACACCCAGGATGAGACCTGCACGCAGTGGCT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3538764..3538873 26863196 MeRIP-seq:(Medium) rs766020501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21892075,Human_RBP_ID_22422285,Human_RBP_ID_25404135 80854 RMVar_ID_80854 Human_SNP_ID_656130039 m1A Human chr19 + 3539246 3539246 3539246 ATCCCCTCGGGGACCCTCGAGGCCAGCTTCCCAGCACCGCTGTACAGGTGAGCCCCTCCCTACAG ATCCCCTCGGGGACCCTCGAGGCCAGCTTCCCGGCACCGCTGTACAGGTGAGCCCCTCCCTACAG A G C19orf71 Ensembl:ENSG00000183397 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3539201..3539480 26863196 MeRIP-seq:(Medium) rs936708418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1937631 80855 RMVar_ID_80855 Human_SNP_ID_656130226 m1A Human chr19 + 3539602 3539602 3539602 GGCCCTTCTGTGGCTGAGAGAGTCTGTCCCACACCTCTTGCAGCCCGTGGTGGCTCTGGGCAACC GGCCCTTCTGTGGCTGAGAGAGTCTGTCCCACGCCTCTTGCAGCCCGTGGTGGCTCTGGGCAACC A G C19orf71 Ensembl:ENSG00000183397 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:3539581..3539679;chr19:3539551..3539681 26863196 MeRIP-seq:(Medium) rs1161145555 Functional Loss SNV dbSNP153 33..33 33 - - - 80856 RMVar_ID_80856 Human_SNP_ID_656131542 m1A Human chr19 + 3542860 3542860 3542860 CAGACCACTTCTTCCTGGTGCACCTCCAGGCCAGGGGGGCTTCCCAGAGGAAGGGACTTGTGGGT CAGACCACTTCTTCCTGGTGCACCTCCAGGCCCGGGGGGCTTCCCAGAGGAAGGGACTTGTGGGT A C C19orf71 Ensembl:ENSG00000183397 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3542834..3542984 32194978 MeRIP-seq:(Medium) rs766848595 Functional Loss SNV dbSNP153 33..33 33 - - - 80857 RMVar_ID_80857 Human_SNP_ID_656131543 m1A Human chr19 + 3542860 3542860 3542860 CAGACCACTTCTTCCTGGTGCACCTCCAGGCCAGGGGGGCTTCCCAGAGGAAGGGACTTGTGGGT CAGACCACTTCTTCCTGGTGCACCTCCAGGCCGGGGGGGCTTCCCAGAGGAAGGGACTTGTGGGT A G C19orf71 Ensembl:ENSG00000183397 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3542834..3542984 32194978 MeRIP-seq:(Medium) rs766848595 Functional Loss SNV dbSNP153 33..33 33 - - - 80858 RMVar_ID_80858 Human_SNP_ID_656131577 m1A Human chr19 + 3542908 3542908 3542908 GGAAGGGACTTGTGGGTCTTGGAGGCTGGACAAGGACTGTAGGAATCCAGGAGTAGCCAGGGCCC GGAAGGGACTTGTGGGTCTTGGAGGCTGGACAGGGACTGTAGGAATCCAGGAGTAGCCAGGGCCC A G C19orf71 Ensembl:ENSG00000183397 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3542899..3543264 26863196 MeRIP-seq:(Medium) rs1363183686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435185 80859 RMVar_ID_80859 Human_SNP_ID_656131672 m1A Human chr19 - 3543090 3543090 3543090 CTCCCTCCCTCGCCACTTGGAGTCTGTCCTTCAGCCCTGTACCCCTCACCCCAGAGTGGGTGCTT CTCCCTCCCTCGCCACTTGGAGTCTGTCCTTCTGCCCTGTACCCCTCACCCCAGAGTGGGTGCTT T A MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3543076..3543100 26863196 MeRIP-seq:(Medium) rs1449396131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908297,Human_RBP_ID_22371079,Human_RBP_ID_27272783,Human_RBP_ID_27467125 80860 RMVar_ID_80860 Human_SNP_ID_656131681 m1A Human chr19 + 3543117 3543117 3543117 AGGGCTGAAGGACAGACTCCAAGTGGCGAGGGAGGGAGACCCCACGCCGTGGGCCAGGCCTCTAC AGGGCTGAAGGACAGACTCCAAGTGGCGAGGGCGGGAGACCCCACGCCGTGGGCCAGGCCTCTAC A C C19orf71 Ensembl:ENSG00000183397 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3543080..3543299 26863196 MeRIP-seq:(Medium) rs1434196321 Functional Loss SNV dbSNP153 33..33 33 - - - 80861 RMVar_ID_80861 Human_SNP_ID_656132125 m1A Human chr19 + 3543654 3543651 3543655 CAGCACCCGGTGGGGGAGCGCGCTGTGGAAAGACAGGCCAATCCGGGGCAAGGAATACGGTGAGG CAGCACCCGGTGGGGGAGCGCGCTGTGGAA____AGGCCAATCCGGGGCAAGGAATACGGTGAGG AAGAC A C19orf71 Ensembl:ENSG00000183397 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3543641..3543934 32194978 MeRIP-seq:(Medium) rs1415595257 Functional Loss DEL dbSNP153 31..34 33 - - - Human_Splice_Rec_1937634,Human_Splice_Rec_1937635 RMVar_hsa_circ_191355 80862 RMVar_ID_80862 Human_SNP_ID_656132128 m1A Human chr19 + 3543654 3543654 3543654 CAGCACCCGGTGGGGGAGCGCGCTGTGGAAAGACAGGCCAATCCGGGGCAAGGAATACGGTGAGG CAGCACCCGGTGGGGGAGCGCGCTGTGGAAAGGCAGGCCAATCCGGGGCAAGGAATACGGTGAGG A G C19orf71 Ensembl:ENSG00000183397 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3543641..3543934 32194978 MeRIP-seq:(Medium) rs1259804819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1937634,Human_Splice_Rec_1937635 RMVar_hsa_circ_191355 80863 RMVar_ID_80863 Human_SNP_ID_656132150 m1A Human chr19 + 3543675 3543675 3543675 GCTGTGGAAAGACAGGCCAATCCGGGGCAAGGAATACGGTGAGGCTAGGTGCAGGGTGGGTCCTT GCTGTGGAAAGACAGGCCAATCCGGGGCAAGGCATACGGTGAGGCTAGGTGCAGGGTGGGTCCTT A C C19orf71 Ensembl:ENSG00000183397 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3543651..3543675 26863196 MeRIP-seq:(Medium) rs1568250651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1937635 RMVar_hsa_circ_191355 80864 RMVar_ID_80864 Human_SNP_ID_656132214 m1A Human chr19 - 3543774 3543774 3543774 CATGTGCCCCCACCTCCTCGCCGTTGGCCAGCAAGGGGCTCCTGGATCGCCCCGGGCAGTTTCAC CATGTGCCCCCACCTCCTCGCCGTTGGCCAGCTAGGGGCTCCTGGATCGCCCCGGGCAGTTTCAC T A MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3543723..3544032 26863196 MeRIP-seq:(Medium) rs1005173664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140394 80865 RMVar_ID_80865 Human_SNP_ID_656132215 m1A Human chr19 - 3543774 3543774 3543774 CATGTGCCCCCACCTCCTCGCCGTTGGCCAGCAAGGGGCTCCTGGATCGCCCCGGGCAGTTTCAC CATGTGCCCCCACCTCCTCGCCGTTGGCCAGCCAGGGGCTCCTGGATCGCCCCGGGCAGTTTCAC T G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3543723..3544032 26863196 MeRIP-seq:(Medium) rs1005173664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140394 80866 RMVar_ID_80866 Human_SNP_ID_656132375 m1A Human chr19 + 3543995 3543995 3543995 TCCACCTGCCAGCGGTCCCCGCCTTCCCTCACACCCACTCCCCGATAAAGGCATGCTACCAGGAT TCCACCTGCCAGCGGTCCCCGCCTTCCCTCACCCCCACTCCCCGATAAAGGCATGCTACCAGGAT A C C19orf71 Ensembl:ENSG00000183397 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3543601..3544062 26863196 MeRIP-seq:(Medium) rs759804585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191355 80867 RMVar_ID_80867 Human_SNP_ID_656132536 m1A Human chr19 - 3544242 3544242 3544242 CCCCACCGTGGTGGGCAGCAGGGCTGCCCGGCAGGCTTGGTGGACTCTGCTGGCAGCAAATAAAG CCCCACCGTGGTGGGCAGCAGGGCTGCCCGGCCGGCTTGGTGGACTCTGCTGGCAGCAAATAAAG T G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3544201..3544275 26863196 MeRIP-seq:(Medium) rs969228739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54313,Human_RBP_ID_519805,Human_RBP_ID_5115991,Human_RBP_ID_5585607,Human_RBP_ID_8484157,Human_RBP_ID_18461079 Human_Splice_Rec_1937544 RMVar_hsa_circ_111303,RMVar_hsa_circ_127723,RMVar_hsa_circ_191357,RMVar_hsa_circ_89361,RMVar_hsa_circ_191358,RMVar_hsa_circ_191356 80868 RMVar_ID_80868 Human_SNP_ID_656132548 m1A Human chr19 + 3544263 3544263 3544263 TCCACCAAGCCTGCCGGGCAGCCCTGCTGCCCACCACGGTGGGGTCCAGGCCCAGCCCACCACCC TCCACCAAGCCTGCCGGGCAGCCCTGCTGCCCCCCACGGTGGGGTCCAGGCCCAGCCCACCACCC A C AC005786.3 Ensembl:ENSG00000267436 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3544214..3544422 26863196 MeRIP-seq:(Medium) rs546364518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191355 80869 RMVar_ID_80869 Human_SNP_ID_656132733 m1A Human chr19 + 3544612 3544607 3544612 GCTGGGTGAGGATGGAGGGTGGGGGTCCAGAGAAGAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG GCTGGGTGAGGATGGAGGGTGGGGGTCC_____AGAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG CAGAGA C AC005786.3 Ensembl:ENSG00000267436 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3544598..3544755 26863196 MeRIP-seq:(Medium) rs1268333065 Functional Loss DEL dbSNP153 29..33 33 - - - 80870 RMVar_ID_80870 Human_SNP_ID_656132734 m1A Human chr19 + 3544612 3544611 3544613 GCTGGGTGAGGATGGAGGGTGGGGGTCCAGAGAAGAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG GCTGGGTGAGGATGGAGGGTGGGGGTCCAGAG__GAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG GAA G AC005786.3 Ensembl:ENSG00000267436 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3544598..3544755 26863196 MeRIP-seq:(Medium) rs143698298 Functional Loss DEL dbSNP153 33..34 33 - - - 80871 RMVar_ID_80871 Human_SNP_ID_656132795 m1A Human chr19 - 3544703 3544703 3544703 CAGGGGACCGTGATGCCCGGCCCTGACTCCTGACAGCCTCCTGCACCTGTGCAAGGGAACTGTGG CAGGGGACCGTGATGCCCGGCCCTGACTCCTGCCAGCCTCCTGCACCTGTGCAAGGGAACTGTGG T G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3544668..3544829 26863196 MeRIP-seq:(Medium) rs199970491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54315,Human_RBP_ID_27467139 Human_Splice_Rec_1937542,Human_Splice_Rec_1937562,Human_Splice_Rec_1937578 RMVar_hsa_circ_111303,RMVar_hsa_circ_127723,RMVar_hsa_circ_191357,RMVar_hsa_circ_89361,RMVar_hsa_circ_191358,RMVar_hsa_circ_191356 80872 RMVar_ID_80872 Human_SNP_ID_656132884 m1A Human chr19 - 3544824 3544795 3544825 CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCCGACCCGCCTGCGACGCTGTGAGTCCTGGCCCACC CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCC______________________________CACC GGGCCAGGACTCACAGCGTCGCAGGCGGGTC G MFSD12 Ensembl:ENSG00000161091 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3544476..3545650;chr19:3544481..3545650 26863196 MeRIP-seq:(Medium) rs780114491 Functional Loss DEL dbSNP153 32..61 33 - - - Human_RBP_ID_519811,Human_RBP_ID_5116573,Human_RBP_ID_5375145,Human_RBP_ID_18728854,Human_RBP_ID_18994055 Human_Splice_Rec_1937515,Human_Splice_Rec_1937521,Human_Splice_Rec_1937541,Human_Splice_Rec_1937561,Human_Splice_Rec_1937577 RMVar_hsa_circ_13529,RMVar_hsa_circ_111303,RMVar_hsa_circ_127723,RMVar_hsa_circ_191357,RMVar_hsa_circ_191358,RMVar_hsa_circ_373333,RMVar_hsa_circ_191359 80873 RMVar_ID_80873 Human_SNP_ID_656132920 m1A Human chr19 - 3544824 3544824 3544824 CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCCGACCCGCCTGCGACGCTGTGAGTCCTGGCCCACC CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCCGTCCCGCCTGCGACGCTGTGAGTCCTGGCCCACC T A MFSD12 Ensembl:ENSG00000161091 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3544476..3545650;chr19:3544481..3545650 26863196 MeRIP-seq:(Medium) rs868784086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519811,Human_RBP_ID_5116573,Human_RBP_ID_5375145,Human_RBP_ID_18728854,Human_RBP_ID_18994055 Human_Splice_Rec_1937515,Human_Splice_Rec_1937521,Human_Splice_Rec_1937541,Human_Splice_Rec_1937561,Human_Splice_Rec_1937577 RMVar_hsa_circ_13529,RMVar_hsa_circ_111303,RMVar_hsa_circ_127723,RMVar_hsa_circ_191357,RMVar_hsa_circ_191358,RMVar_hsa_circ_373333,RMVar_hsa_circ_191359 80874 RMVar_ID_80874 Human_SNP_ID_656132921 m1A Human chr19 - 3544824 3544824 3544824 CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCCGACCCGCCTGCGACGCTGTGAGTCCTGGCCCACC CCCTGTGTCTCTGTAGCCTCCTGCTGTGGCCGCCCCGCCTGCGACGCTGTGAGTCCTGGCCCACC T G MFSD12 Ensembl:ENSG00000161091 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3544476..3545650;chr19:3544481..3545650 26863196 MeRIP-seq:(Medium) rs868784086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519811,Human_RBP_ID_5116573,Human_RBP_ID_5375145,Human_RBP_ID_18728854,Human_RBP_ID_18994055 Human_Splice_Rec_1937515,Human_Splice_Rec_1937521,Human_Splice_Rec_1937541,Human_Splice_Rec_1937561,Human_Splice_Rec_1937577 RMVar_hsa_circ_13529,RMVar_hsa_circ_111303,RMVar_hsa_circ_127723,RMVar_hsa_circ_191357,RMVar_hsa_circ_191358,RMVar_hsa_circ_373333,RMVar_hsa_circ_191359 80875 RMVar_ID_80875 Human_SNP_ID_656133093 m1A Human chr19 + 3544981 3544978 3544982 GAGGCGGGGGATGAGTAGGCACCGCGGGTACCACCCCCCCGCCACCCAAGCTGAACCTGTGCCTC GAGGCGGGGGATGAGTAGGCACCGCGGGTA____CCCCCCGCCACCCAAGCTGAACCTGTGCCTC ACCAC A AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3544976..3545350 26863196 MeRIP-seq:(Medium) rs775020140 Functional Loss DEL dbSNP153 31..34 33 - - - 80876 RMVar_ID_80876 Human_SNP_ID_656133100 m1A Human chr19 + 3544981 3544981 3544981 GAGGCGGGGGATGAGTAGGCACCGCGGGTACCACCCCCCCGCCACCCAAGCTGAACCTGTGCCTC GAGGCGGGGGATGAGTAGGCACCGCGGGTACCCCCCCCCCGCCACCCAAGCTGAACCTGTGCCTC A C AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3544976..3545350 26863196 MeRIP-seq:(Medium) rs765712393 Functional Loss SNV dbSNP153 33..33 33 - - - 80877 RMVar_ID_80877 Human_SNP_ID_656133101 m1A Human chr19 + 3544981 3544981 3544981 GAGGCGGGGGATGAGTAGGCACCGCGGGTACCACCCCCCCGCCACCCAAGCTGAACCTGTGCCTC GAGGCGGGGGATGAGTAGGCACCGCGGGTACCGCCCCCCCGCCACCCAAGCTGAACCTGTGCCTC A G AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3544976..3545350 26863196 MeRIP-seq:(Medium) rs765712393 Functional Loss SNV dbSNP153 33..33 33 - - - 80878 RMVar_ID_80878 Human_SNP_ID_656133929 m1A Human chr19 + 3546321 3546315 3546322 AGCGAGGTGACGAGGATGGTGGCACAGCCAGCACCCAGCAGCACAGCCGCTGCGTACACGGCCAC AGCGAGGTGACGAGGATGGTGGCACAG_______CCAGCAGCACAGCCGCTGCGTACACGGCCAC GCCAGCAC G AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3546187..3546352 26863196 MeRIP-seq:(Medium) rs757747148 Functional Loss DEL dbSNP153 28..34 33 - - - 80879 RMVar_ID_80879 Human_SNP_ID_656134036 m1A Human chr19 + 3546454 3546454 3546454 TCATCTGCAGGGACAGCCCCGGGGTCAGGCCCACACCACTGGGTGCCCCCAAGCCTGGCGCTTCA TCATCTGCAGGGACAGCCCCGGGGTCAGGCCCGCACCACTGGGTGCCCCCAAGCCTGGCGCTTCA A G AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3546451..3546475 26863196 MeRIP-seq:(Medium) rs758675212 Functional Loss SNV dbSNP153 33..33 33 - - - 80880 RMVar_ID_80880 Human_SNP_ID_656134812 m1A Human chr19 - 3547925 3547925 3547925 GCCGGCCGCATGCGGAGGAGCCAGGCGAGCACACCCCCCTGTTGGCCCCTGCCACGGCCCAGCCC GCCGGCCGCATGCGGAGGAGCCAGGCGAGCACCCCCCCCTGTTGGCCCCTGCCACGGCCCAGCCC T G MFSD12 Ensembl:ENSG00000161091 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3547874..3547976 26863196 MeRIP-seq:(Medium) rs903251736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18470398,Human_RBP_ID_22446316 Human_Splice_Rec_1937531,Human_Splice_Rec_1937551,Human_Splice_Rec_1937567,Human_Splice_Rec_1937589,Human_Splice_Rec_1937603,Human_Splice_Rec_1937611 RMVar_hsa_circ_30349,RMVar_hsa_circ_13529,RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_320710,RMVar_hsa_circ_191361,RMVar_hsa_circ_298240,RMVar_hsa_circ_191364,RMVar_hsa_circ_49224,RMVar_hsa_circ_191363,RMVar_hsa_circ_117087,RMVar_hsa_circ_191365 80881 RMVar_ID_80881 Human_SNP_ID_656134863 m1A Human chr19 + 3548005 3548002 3548005 CCAGGTGGAATAGCAGTGAGAACACGGCGCCGACACCCACCACCAGCAGGGACAGGTTCTGGGGA CCAGGTGGAATAGCAGTGAGAACACGGCGC___CACCCACCACCAGCAGGGACAGGTTCTGGGGA CCGA C AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3547826..3548150 26863196 MeRIP-seq:(Medium) rs778505146 Functional Loss DEL dbSNP153 31..33 33 - - - 80882 RMVar_ID_80882 Human_SNP_ID_656134882 m1A Human chr19 - 3548032 3548032 3548032 CCGCCACCACTGACTGCTTCTGCTGCATCCCCAGAACCTGTCCCTGCTGGTGGTGGGTGTCGGCG CCGCCACCACTGACTGCTTCTGCTGCATCCCCGGAACCTGTCCCTGCTGGTGGTGGGTGTCGGCG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3547999..3548143;chr19:3548027..3548110 26863196 MeRIP-seq:(Medium) rs111261494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435254 RMVar_hsa_circ_13529,RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_320710,RMVar_hsa_circ_191361,RMVar_hsa_circ_298240,RMVar_hsa_circ_191364,RMVar_hsa_circ_49224,RMVar_hsa_circ_191363 80883 RMVar_ID_80883 Human_SNP_ID_656136179 m1A Human chr19 + 3551063 3551063 3551063 CGGGATGAGGCTGAGGTGGGAGATCTGTGTGGAGGCCCAGCCAAACTGGAAGATCACGATGAACG CGGGATGAGGCTGAGGTGGGAGATCTGTGTGGTGGCCCAGCCAAACTGGAAGATCACGATGAACG A T AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3551026..3557236 26863196 MeRIP-seq:(Medium) rs1568260632 Functional Loss SNV dbSNP153 33..33 33 - - - 80884 RMVar_ID_80884 Human_SNP_ID_656136185 m1A Human chr19 - 3551077 3551077 3551077 CCTCTACTACGGCCCGTTCATCGTGATCTTCCAGTTTGGCTGGGCCTCCACACAGATCTCCCACC CCTCTACTACGGCCCGTTCATCGTGATCTTCCTGTTTGGCTGGGCCTCCACACAGATCTCCCACC T A MFSD12 Ensembl:ENSG00000161091 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3551026..3557600 26863196 MeRIP-seq:(Medium) rs201324028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8832443,Human_RBP_ID_13435440,Human_RBP_ID_17272254,Human_RBP_ID_18191750,Human_RBP_ID_26988501 Human_Splice_Rec_1937527,Human_Splice_Rec_1937547,Human_Splice_Rec_1937563,Human_Splice_Rec_1937585,Human_Splice_Rec_1937599,Human_Splice_Rec_1937617 RMVar_hsa_circ_13529,RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_320710,RMVar_hsa_circ_191361,RMVar_hsa_circ_191364,RMVar_hsa_circ_49224,RMVar_hsa_circ_191367,RMVar_hsa_circ_96964,RMVar_hsa_circ_287222,RMVar_hsa_circ_191366 80885 RMVar_ID_80885 Human_SNP_ID_656136205 m1A Human chr19 + 3551107 3551105 3551108 ACTGGAAGATCACGATGAACGGGCCGTAGTAGAGGAGGGCAGCCCACTCGGGCGTGGCCGCCCCA ACTGGAAGATCACGATGAACGGGCCGTAGTA___GAGGGCAGCCCACTCGGGCGTGGCCGCCCCA AGAG A AC005786.3 Ensembl:ENSG00000267436 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3551056..3551143 26863196 MeRIP-seq:(Medium) rs1486664170 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13435452 80886 RMVar_ID_80886 Human_SNP_ID_656136257 m1A Human chr19 - 3551196 3551196 3551196 ACAGCCCCGCGACTGACCACTCTGCCTTCCACAGGCACCGTCTGCGTCCTGCTGTCCTTCCCCTT ACAGCCCCGCGACTGACCACTCTGCCTTCCACGGGCACCGTCTGCGTCCTGCTGTCCTTCCCCTT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3551151..3551225 26863196 MeRIP-seq:(Medium) rs923454411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22663476 RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 80887 RMVar_ID_80887 Human_SNP_ID_656136277 m1A Human chr19 - 3551228 3551228 3551228 GTCCTCACCCTGGGAGCCCTGGCTGGTGCGGGACAGCCCCGCGACTGACCACTCTGCCTTCCACA GTCCTCACCCTGGGAGCCCTGGCTGGTGCGGGGCAGCCCCGCGACTGACCACTCTGCCTTCCACA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3551226..3551250 26863196 MeRIP-seq:(Medium) rs1438135198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22663476 RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 80888 RMVar_ID_80888 Human_SNP_ID_656136524 m1A Human chr19 - 3551942 3551942 3551942 GCCAGTCTTGCTAAGATGTGAGAGAGAGCTCTAGGCAGAGGCACGCCCATGCAAAGGCCCGGGGG GCCAGTCTTGCTAAGATGTGAGAGAGAGCTCTGGGCAGAGGCACGCCCATGCAAAGGCCCGGGGG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3551581..3552150 26863196 MeRIP-seq:(Medium) rs912912875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585621,Human_RBP_ID_13435509 RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 80889 RMVar_ID_80889 Human_SNP_ID_656138044 m1A Human chr19 - 3556552 3556552 3556552 GTGCTGTGCCTCCCCCATCTGTCTGACTGTGCAGTGCCTCCCCCATCTGTCCAACTGTGCAGGGC GTGCTGTGCCTCCCCCATCTGTCTGACTGTGCTGTGCCTCCCCCATCTGTCCAACTGTGCAGGGC T A MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:3556526..3556925 26863196 MeRIP-seq:(Medium) rs1208416322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3585418,Human_RBP_ID_18946256,Human_RBP_ID_20349292 RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 80890 RMVar_ID_80890 Human_SNP_ID_656138493 m1A Human chr19 - 3557523 3557523 3557523 CGTGGGTGAGGGCGCGGCCGTAAGAGAGCGGGACGCGGGGTGCCCGGCGCGTGGTGGGGGTCCCC CGTGGGTGAGGGCGCGGCCGTAAGAGAGCGGGGCGCGGGGTGCCCGGCGCGTGGTGGGGGTCCCC T C MFSD12 Ensembl:ENSG00000161091 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr19:3557430..3557561;chr19:3557426..3557566 26863196,26863410 MeRIP-seq:(Medium) rs1383447858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55481,Human_RBP_ID_825189,Human_RBP_ID_4557093,Human_RBP_ID_5526771,Human_RBP_ID_8942145,Human_RBP_ID_22447173 RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364 80891 RMVar_ID_80891 Human_SNP_ID_656143471 m1A Human chr19 + 3573310 3573310 3573310 CGTCCGTGTTCCAGGTCCGGCCCGGAGCGGCCATGTCCCACGGCCCCAAGCAGCCCGGCGCGGCC CGTCCGTGTTCCAGGTCCGGCCCGGAGCGGCCCTGTCCCACGGCCCCAAGCAGCCCGGCGCGGCC A C HMG20B Ensembl:ENSG00000064961 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3572951..3573395 26863196 MeRIP-seq:(Medium) rs1199980587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239103,Human_RBP_ID_824042,Human_RBP_ID_907089,Human_RBP_ID_4520557,Human_RBP_ID_8233570,Human_RBP_ID_9294069,Human_RBP_ID_9328337,Human_RBP_ID_9380079,Human_RBP_ID_18420829,Human_RBP_ID_18996007,Human_RBP_ID_22448163,Human_RBP_ID_22977352,Human_RBP_ID_26335172,Human_RBP_ID_27814904 Human_Splice_Rec_1937640,Human_Splice_Rec_1937641,Human_Splice_Rec_1937654,Human_Splice_Rec_1937655,Human_Splice_Rec_1937658,Human_Splice_Rec_1937659,Human_Splice_Rec_1937676,Human_Splice_Rec_1937677,Human_Splice_Rec_1937683,Human_Splice_Rec_1937690,Human_Splice_Rec_1937691,Human_Splice_Rec_1937701,Human_Splice_Rec_1937716,Human_Splice_Rec_1937717 RMVar_hsa_circ_112098,RMVar_hsa_circ_34154,RMVar_hsa_circ_191368 80892 RMVar_ID_80892 Human_SNP_ID_656144433 m1A Human chr19 - 3575521 3575521 3575521 TCATCCAGGTACCGCTGGGGGGCAGCACCAGAAGGCTTGAAGCAGGGGAAGCCTCCAACGCCAGG TCATCCAGGTACCGCTGGGGGGCAGCACCAGAGGGCTTGAAGCAGGGGAAGCCTCCAACGCCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3575518..3575650 32194978 MeRIP-seq:(Medium) rs1195567930 Functional Loss SNV dbSNP153 33..33 33 - - - 80893 RMVar_ID_80893 Human_SNP_ID_656144493 m1A Human chr19 + 3575643 3575643 3575643 AGCCTATAAGATGTGCACGGAGAAGATCCAGGAGAAGAAGATCAAGAAAGGTGGGAGGGGTCGGG AGCCTATAAGATGTGCACGGAGAAGATCCAGGGGAAGAAGATCAAGAAAGGTGGGAGGGGTCGGG A G HMG20B Ensembl:ENSG00000064961 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3575223..3575737 26863196 MeRIP-seq:(Medium) rs775904095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519887,Human_RBP_ID_914589,Human_RBP_ID_1884501,Human_RBP_ID_3568663,Human_RBP_ID_8255977,Human_RBP_ID_8484254,Human_RBP_ID_9380084,Human_RBP_ID_18412441,Human_RBP_ID_18996011,Human_RBP_ID_24545614,Human_RBP_ID_26335180,Human_RBP_ID_27814906 Human_Splice_Rec_1937647,Human_Splice_Rec_1937665,Human_Splice_Rec_1937697,Human_Splice_Rec_1937705,Human_Splice_Rec_1937723,Human_Splice_Rec_1937733 RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_34154,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_191370 80894 RMVar_ID_80894 Human_SNP_ID_656144627 m1A Human chr19 + 3575965 3575962 3575966 GACTCCGTCTCAAAAAAAAAAAAAAAAGAAAAAGAAAAATGAAAGGTGGGAGGGGCCGGTGCGAG GACTCCGTCTCAAAAAAAAAAAAAAAAGAA____AAAAATGAAAGGTGGGAGGGGCCGGTGCGAG AAAAG A HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3575962..3576375 26863196 MeRIP-seq:(Medium) rs1383353111 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_191370 80895 RMVar_ID_80895 Human_SNP_ID_656144628 m1A Human chr19 + 3575965 3575963 3575966 GACTCCGTCTCAAAAAAAAAAAAAAAAGAAAAAGAAAAATGAAAGGTGGGAGGGGCCGGTGCGAG GACTCCGTCTCAAAAAAAAAAAAAAAAGAAA___AAAAATGAAAGGTGGGAGGGGCCGGTGCGAG AAAG A HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3575962..3576375 26863196 MeRIP-seq:(Medium) rs1423172756 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_191370 80896 RMVar_ID_80896 Human_SNP_ID_656144629 m1A Human chr19 + 3575965 3575964 3575966 GACTCCGTCTCAAAAAAAAAAAAAAAAGAAAAAGAAAAATGAAAGGTGGGAGGGGCCGGTGCGAG GACTCCGTCTCAAAAAAAAAAAAAAAAGAAAA__AAAAATGAAAGGTGGGAGGGGCCGGTGCGAG AAG A HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3575962..3576375 26863196 MeRIP-seq:(Medium) rs1231530524 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_191370 80897 RMVar_ID_80897 Human_SNP_ID_656145055 m1A Human chr19 + 3577032 3577032 3577032 TGGAGCAGGAGCTGGCGCTGGAGGAGCGGAGGACGCTGGCGCTGCAGCAGCAGCTCCAGGCCGTG TGGAGCAGGAGCTGGCGCTGGAGGAGCGGAGGGCGCTGGCGCTGCAGCAGCAGCTCCAGGCCGTG A G HMG20B Ensembl:ENSG00000064961 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3576833..3577142 26863196 MeRIP-seq:(Medium) rs757701879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519925,Human_RBP_ID_26335183 Human_Splice_Rec_1937671,Human_Splice_Rec_1937711,Human_Splice_Rec_1937741,Human_Splice_Rec_1937749,Human_Splice_Rec_1937753,Human_Splice_Rec_1937757 RMVar_hsa_circ_95698,RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_119955,RMVar_hsa_circ_191370,RMVar_hsa_circ_191371,RMVar_hsa_circ_191372 80898 RMVar_ID_80898 Human_SNP_ID_656145224 m1A Human chr19 + 3577251 3577251 3577251 GTCCCCTCTTCCCCAGTCACCCGGCCCCGCCTATCGCCCCGCCCTCATCACCCCCAGCTCCGCCT GTCCCCTCTTCCCCAGTCACCCGGCCCCGCCTGTCGCCCCGCCCTCATCACCCCCAGCTCCGCCT A G HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3577243..3577317 26863196 MeRIP-seq:(Medium) rs1373090357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95698,RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_119955,RMVar_hsa_circ_191370,RMVar_hsa_circ_191371,RMVar_hsa_circ_191372 80899 RMVar_ID_80899 Human_SNP_ID_656145346 m1A Human chr19 - 3577494 3577494 3577494 GAGAGGGGCCAGCGACGGTGGGGCCGGTAGGGAGCGGTGGGGGCGCGAAGGGTGGGGGCACAAAG GAGAGGGGCCAGCGACGGTGGGGCCGGTAGGGGGCGGTGGGGGCGCGAAGGGTGGGGGCACAAAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3577476..3577550 26863196 MeRIP-seq:(Medium) rs1413068164 Functional Loss SNV dbSNP153 33..33 33 - - - 80900 RMVar_ID_80900 Human_SNP_ID_656145448 m1A Human chr19 + 3577710 3577710 3577710 CCACGCGACCCCAGCCCCCCGGTGTCATCCCCACCTCCCCGACCTCGTTCCCTCCGTCCGTGACT CCACGCGACCCCAGCCCCCCGGTGTCATCCCCTCCTCCCCGACCTCGTTCCCTCCGTCCGTGACT A T HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3577701..3577775 26863196 MeRIP-seq:(Medium) rs1372926491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082205 RMVar_hsa_circ_95698,RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_119955,RMVar_hsa_circ_191370,RMVar_hsa_circ_191371,RMVar_hsa_circ_191372 80901 RMVar_ID_80901 Human_SNP_ID_656145539 m1A Human chr19 - 3577941 3577941 3577941 ACAGGCGGGAAGGTCAGGCGAGGGTGCCGGGGAGTCGCGGGGCGGGGGCTCCAGGGGCAGCGGTA ACAGGCGGGAAGGTCAGGCGAGGGTGCCGGGGGGTCGCGGGGCGGGGGCTCCAGGGGCAGCGGTA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3577926..3577975 26863196 MeRIP-seq:(Medium) rs980545509 Functional Loss SNV dbSNP153 33..33 33 - - - 80902 RMVar_ID_80902 Human_SNP_ID_656145966 m1A Human chr19 - 3578725 3578708 3578726 CTGTGAGGTTCTTCTGGGTGTATCGCGCAGCGAGTGCTTTTTCCGGGTTCAGGGGGCTGGGGAGA CTGTGAGGTTCTTCTGGGTGTATCGCGCAGC__________________CAGGGGGCTGGGGAGA GAACCCGGAAAAAGCACTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3578498..3578980 26863196 MeRIP-seq:(Medium) rs1296268996 Functional Loss DEL dbSNP153 32..49 33 - - - 80903 RMVar_ID_80903 Human_SNP_ID_656145976 m1A Human chr19 - 3578729 3578726 3578729 TCGGCTGTGAGGTTCTTCTGGGTGTATCGCGCAGCGAGTGCTTTTTCCGGGTTCAGGGGGCTGGG TCGGCTGTGAGGTTCTTCTGGGTGTATCGCGC___GAGTGCTTTTTCCGGGTTCAGGGGGCTGGG CGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:3578491..3579050;chr19:3578509..3578987 26863196 MeRIP-seq:(Medium) rs3833282 Functional Loss DEL dbSNP153 33..35 33 - - - 80904 RMVar_ID_80904 Human_SNP_ID_656145990 m1A Human chr19 + 3578745 3578742 3578745 CGGAAAAAGCACTCGCTGCGCGATACACCCAGAAGAACCTCACAGCCGAGGGTGCCCCTCCTCGG CGGAAAAAGCACTCGCTGCGCGATACACCC___AGAACCTCACAGCCGAGGGTGCCCCTCCTCGG CAGA C HMG20B Ensembl:ENSG00000064961 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3578601..3578850 26863196 MeRIP-seq:(Medium) rs1568274110 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_519955,Human_RBP_ID_1014915,Human_RBP_ID_5117265,Human_RBP_ID_9086831,Human_RBP_ID_17656585 Human_Splice_Rec_1937756 Human_miRNA_ID_2007725,Human_miRNA_ID_2673397 RMVar_hsa_circ_95698,RMVar_hsa_circ_76110,RMVar_hsa_circ_112098,RMVar_hsa_circ_191368,RMVar_hsa_circ_90041,RMVar_hsa_circ_191369,RMVar_hsa_circ_119955,RMVar_hsa_circ_191370,RMVar_hsa_circ_191371,RMVar_hsa_circ_191372 80905 RMVar_ID_80905 Human_SNP_ID_656153232 m1A Human chr19 + 3600439 3600439 3600439 CAGGAAGTCGGTGAGGACGAGGCCGCAGAGGAAGGTGAGGAAGGAGGAGCGCGTGTGCGAACCCC CAGGAAGTCGGTGAGGACGAGGCCGCAGAGGAGGGTGAGGAAGGAGGAGCGCGTGTGCGAACCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3600391..3600543 26863196 MeRIP-seq:(Medium) rs200164976 Functional Loss SNV dbSNP153 33..33 33 - - - 80906 RMVar_ID_80906 Human_SNP_ID_656154284 m1A Human chr19 - 3603337 3603337 3603337 CCTCTGGAAGCCCTGCCTCCCACCACGGTGGCAGTGGCCTTAGCTGTCTTCCCAGGAAGGGAGTT CCTCTGGAAGCCCTGCCTCCCACCACGGTGGCGGTGGCCTTAGCTGTCTTCCCAGGAAGGGAGTT T C TBXA2R Ensembl:ENSG00000006638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3603326..3603399 26863196 MeRIP-seq:(Medium) rs1386445389 Functional Loss SNV dbSNP153 33..33 33 - - - 80907 RMVar_ID_80907 Human_SNP_ID_656155018 m1A Human chr19 + 3605874 3605874 3605874 AGCAGAAACACAACAGACACACAGCCACACACAGACACATACAGGCAGAAACACGACAGACATAG AGCAGAAACACAACAGACACACAGCCACACACGGACACATACAGGCAGAAACACGACAGACATAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3605862..3606602 26863196 MeRIP-seq:(Medium) rs1365360682 Functional Loss SNV dbSNP153 33..33 33 - - - 80908 RMVar_ID_80908 Human_SNP_ID_656155163 m1A Human chr19 - 3606397 3606397 3606397 CGCAAAGCCCGCGGTGACAGCGGCCAGGTGCCAGGTGTCCCCTGTGTGGCCCGGCGGGTGGCATG CGCAAAGCCCGCGGTGACAGCGGCCAGGTGCCGGGTGTCCCCTGTGTGGCCCGGCGGGTGGCATG T C TBXA2R Ensembl:ENSG00000006638 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3606387..3606536 26863196 MeRIP-seq:(Medium) rs1035786993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23793560 80909 RMVar_ID_80909 Human_SNP_ID_656155237 m1A Human chr19 + 3606721 3606721 3606721 CCCAGGGAAACTGAGTCAGTCTGGCTGTGACCAGGGGCGGGCCCAGCAGAGGACCCACACAGATG CCCAGGGAAACTGAGTCAGTCTGGCTGTGACCTGGGGCGGGCCCAGCAGAGGACCCACACAGATG A T CACTIN-AS1 RNACentral:URS0000D58EBF lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3606685..3606838 26863196 MeRIP-seq:(Medium) rs5741 Functional Loss SNV dbSNP153 33..33 33 - - - 80910 RMVar_ID_80910 Human_SNP_ID_656156582 m1A Human chr19 - 3611127 3611127 3611127 CCCCCCACCTCTGAGCACAGGGCCTGGAGGGCAGGGGCTCCCCGAAGGCTGGGGGTTGGAGAAGG CCCCCCACCTCTGAGCACAGGGCCTGGAGGGCGGGGGCTCCCCGAAGGCTGGGGGTTGGAGAAGG T C CACTIN Ensembl:ENSG00000105298 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3611086..3611732 32194978 MeRIP-seq:(Medium) rs1399966336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26471787,Human_RBP_ID_27467233 80911 RMVar_ID_80911 Human_SNP_ID_656157579 m1A Human chr19 + 3613251 3613245 3613251 ATGAGCACCGCCTCGCCCTCGCCCTCGCCCTCACCGTCCCCGTCGCCGTCGCCCTCTGTCGGGGT ATGAGCACCGCCTCGCCCTCGCCCTCG______CCGTCCCCGTCGCCGTCGCCCTCTGTCGGGGT GCCCTCA G CACTIN-AS1 Ensembl:ENSG00000226800 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3613150..3613318 26863410 MeRIP-seq:(Medium) rs770494441 Functional Loss DEL dbSNP153 28..33 33 - - - 80912 RMVar_ID_80912 Human_SNP_ID_656157585 m1A Human chr19 + 3613251 3613251 3613251 ATGAGCACCGCCTCGCCCTCGCCCTCGCCCTCACCGTCCCCGTCGCCGTCGCCCTCTGTCGGGGT ATGAGCACCGCCTCGCCCTCGCCCTCGCCCTCGCCGTCCCCGTCGCCGTCGCCCTCTGTCGGGGT A G CACTIN-AS1 Ensembl:ENSG00000226800 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3613150..3613318 26863410 MeRIP-seq:(Medium) rs201062195 Functional Loss SNV dbSNP153 33..33 33 - - - 80913 RMVar_ID_80913 Human_SNP_ID_656157597 m1A Human chr19 - 3613261 3613261 3613261 GGACGGCGCGACCCCGACAGAGGGCGACGGCGACGGGGACGGTGAGGGCGAGGGCGAGGGCGAGG GGACGGCGCGACCCCGACAGAGGGCGACGGCGGCGGGGACGGTGAGGGCGAGGGCGAGGGCGAGG T C CACTIN Ensembl:ENSG00000105298 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3613047..3613565 26863196 MeRIP-seq:(Medium) rs758640325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265260 80914 RMVar_ID_80914 Human_SNP_ID_656157945 m1A Human chr19 + 3613928 3613928 3613928 AACAAGCATGATAAATTTAGAGACATTTACAAATTAGCAGAGGAGACATGTATTTACACAGCGGT AACAAGCATGATAAATTTAGAGACATTTACAATTTAGCAGAGGAGACATGTATTTACACAGCGGT A T CACTIN-AS1 Ensembl:ENSG00000226800 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3613923..3614018 26863196 MeRIP-seq:(Medium) rs1261262264 Functional Loss SNV dbSNP153 33..33 33 - - - 80915 RMVar_ID_80915 Human_SNP_ID_656158250 m1A Human chr19 - 3614686 3614681 3614686 TGGATGGGACCCCTGTGGGGGAAGAGGAGGGGAGGGGGACCCCCCCATGGCAGGGGAGGAGGCCC TGGATGGGACCCCTGTGGGGGAAGAGGAGGGG_____GACCCCCCCATGGCAGGGGAGGAGGCCC CCCCCT C CACTIN Ensembl:ENSG00000105298 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3614661..3614761 26863196 MeRIP-seq:(Medium) rs1435518143 Functional Loss DEL dbSNP153 33..37 33 - - - 80916 RMVar_ID_80916 Human_SNP_ID_656158464 m1A Human chr19 + 3615380 3615380 3615380 GGCGGCCTCAGTGCTGCTCTCAGGCCACTTCCACCCACCCCGCTGGGTCTGGCCTCACCTCGCAA GGCGGCCTCAGTGCTGCTCTCAGGCCACTTCCCCCCACCCCGCTGGGTCTGGCCTCACCTCGCAA A C CACTIN-AS1,CACTIN-AS1:2 RNACentral:URS00008C2E2F,RNACentral:URS00008BE755 lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3615355..3615554 26863196 MeRIP-seq:(Medium) rs1273218918 Functional Loss SNV dbSNP153 33..33 33 - - - 80917 RMVar_ID_80917 Human_SNP_ID_656163596 m1A Human chr19 + 3630433 3630428 3630434 CCCTGGGGGGAGTTAAGACACACGAGGTTTGCAGTTTCATTTTGTTTCAGAATCAGTTTGGCCAT CCCTGGGGGGAGTTAAGACACACGAGGT______TTTCATTTTGTTTCAGAATCAGTTTGGCCAT TTTGCAG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3630407..3630595 26863196 MeRIP-seq:(Medium) rs1413465249 Functional Loss DEL dbSNP153 29..34 33 - - - 80918 RMVar_ID_80918 Human_SNP_ID_656164442 m1A Human chr19 - 3633000 3632999 3633000 TGCACGGATGCCGACGGCCGGGCCCCTCCCCGACAAGCCTCCCAGGGCCCCGGCACCCCGGTCGG TGCACGGATGCCGACGGCCGGGCCCCTCCCCG_CAAGCCTCCCAGGGCCCCGGCACCCCGGTCGG GT G PIP5K1C Ensembl:ENSG00000186111 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3632962..3633166 26863196 MeRIP-seq:(Medium) rs1459333240 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_27467379 Human_miRNA_ID_1035932 80919 RMVar_ID_80919 Human_SNP_ID_656165037 m1A Human chr19 - 3634312 3634311 3634312 AGAAAGCAGAGCAGCCTAGGGGCAGGAGAAGCAGGGGGAGCTTGAGGGGGTGGGGGCTCCTCAGG AGAAAGCAGAGCAGCCTAGGGGCAGGAGAAGC_GGGGGAGCTTGAGGGGGTGGGGGCTCCTCAGG CT C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:3634303..3634688;chr19:3634297..3634804 26863196 MeRIP-seq:(Medium) rs750387209 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22718819 RMVar_hsa_circ_265258 80920 RMVar_ID_80920 Human_SNP_ID_656165038 m1A Human chr19 - 3634312 3634312 3634312 AGAAAGCAGAGCAGCCTAGGGGCAGGAGAAGCAGGGGGAGCTTGAGGGGGTGGGGGCTCCTCAGG AGAAAGCAGAGCAGCCTAGGGGCAGGAGAAGCGGGGGGAGCTTGAGGGGGTGGGGGCTCCTCAGG T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:3634303..3634688;chr19:3634297..3634804 26863196 MeRIP-seq:(Medium) rs1312947122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22718819 RMVar_hsa_circ_265258 80921 RMVar_ID_80921 Human_SNP_ID_656166553 m1A Human chr19 - 3638841 3638841 3638841 CGGGCTCCTCCTGCCGCCGGCTCGTCAACCGGACTCTCTCTCACACACGCTCCACCGTGTGCACA CGGGCTCCTCCTGCCGCCGGCTCGTCAACCGGGCTCTCTCTCACACACGCTCCACCGTGTGCACA T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3638839..3638939 26863196 MeRIP-seq:(Medium) rs778293100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203877,Human_RBP_ID_263669 RMVar_hsa_circ_265258 80922 RMVar_ID_80922 Human_SNP_ID_656166559 m1A Human chr19 - 3638847 3638847 3638847 GTGCCCCGGGCTCCTCCTGCCGCCGGCTCGTCAACCGGACTCTCTCTCACACACGCTCCACCGTG GTGCCCCGGGCTCCTCCTGCCGCCGGCTCGTCCACCGGACTCTCTCTCACACACGCTCCACCGTG T G PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3638843..3638970 26863196 MeRIP-seq:(Medium) rs1271370484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203877,Human_RBP_ID_263669 RMVar_hsa_circ_265258 80923 RMVar_ID_80923 Human_SNP_ID_656177921 m1A Human chr19 + 3672257 3672257 3672257 CTCCACGGGGCCACATGGCCGCCTCTGCACCCAGCTGTTCCCTGGCCTGCGCCTGGTCTCCGCCC CTCCACGGGGCCACATGGCCGCCTCTGCACCCGGCTGTTCCCTGGCCTGCGCCTGGTCTCCGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3672253..3672386 26863196 MeRIP-seq:(Medium) rs958984466 Functional Loss SNV dbSNP153 33..33 33 - - - 80924 RMVar_ID_80924 Human_SNP_ID_656185456 m1A Human chr19 + 3694379 3694379 3694379 TGCTTTGGGGGTCCCCACTGCCTGCTCACCCCACATCGGCACACACCTGCCACAGTGCCTGGGCT TGCTTTGGGGGTCCCCACTGCCTGCTCACCCCGCATCGGCACACACCTGCCACAGTGCCTGGGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3694376..3694639 26863196 MeRIP-seq:(Medium) rs1200670027 Functional Loss SNV dbSNP153 33..33 33 - - - 80925 RMVar_ID_80925 Human_SNP_ID_656186381 m1A Human chr19 + 3696977 3696975 3696978 CTCAGGGGGCAAAGGAGGACTGAGCTGGACCGAGGAGGACTGAGCTGGACGGAGGAGGATCGAGC CTCAGGGGGCAAAGGAGGACTGAGCTGGACC___GAGGACTGAGCTGGACGGAGGAGGATCGAGC CGAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3696972..3697197 26863196 MeRIP-seq:(Medium) rs911793446 Functional Loss DEL dbSNP153 32..34 33 - - - 80926 RMVar_ID_80926 Human_SNP_ID_656186383 m1A Human chr19 + 3696977 3696975 3696977 CTCAGGGGGCAAAGGAGGACTGAGCTGGACCGAGGAGGACTGAGCTGGACGGAGGAGGATCGAGC CTCAGGGGGCAAAGGAGGACTGAGCTGGACC__GGAGGACTGAGCTGGACGGAGGAGGATCGAGC CGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3696972..3697197 26863196 MeRIP-seq:(Medium) rs1354338332 Functional Loss DEL dbSNP153 32..33 33 - - - 80927 RMVar_ID_80927 Human_SNP_ID_656186485 m1A Human chr19 + 3697121 3697121 3697121 CTGGACCGAGGAGGACCAAGGAGGACCGAGCCAGACGAAGGAGGACTGAGCCGGACGAAGGAGAA CTGGACCGAGGAGGACCAAGGAGGACCGAGCCGGACGAAGGAGGACTGAGCCGGACGAAGGAGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3697119..3697236 26863196 MeRIP-seq:(Medium) rs1161529142 Functional Loss SNV dbSNP153 33..33 33 - - - 80928 RMVar_ID_80928 Human_SNP_ID_656187680 m1A Human chr19 - 3700128 3700128 3700128 GTCCCCTGGAGCCGCGGGGAGGACGGGGCTGAAGCCGCGCCGGGAAGCGGGAGGCCTGCGAGGGG GTCCCCTGGAGCCGCGGGGAGGACGGGGCTGACGCCGCGCCGGGAAGCGGGAGGCCTGCGAGGGG T G PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3700120..3700429 26863196 MeRIP-seq:(Medium) rs1321547908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203879,Human_RBP_ID_263700,Human_RBP_ID_3580509,Human_RBP_ID_5145593,Human_RBP_ID_5320025,Human_RBP_ID_5372834,Human_RBP_ID_8099997,Human_RBP_ID_8195757,Human_RBP_ID_8942151,Human_RBP_ID_9328360,Human_RBP_ID_17387145,Human_RBP_ID_17655297,Human_RBP_ID_18461088,Human_RBP_ID_18489745,Human_RBP_ID_22416699,Human_RBP_ID_22699312,Human_RBP_ID_22719836,Human_RBP_ID_22741607,Human_RBP_ID_24419308,Human_RBP_ID_26784243 RMVar_hsa_circ_98930,RMVar_hsa_circ_87171,RMVar_hsa_circ_191395,RMVar_hsa_circ_191398 80929 RMVar_ID_80929 Human_SNP_ID_656195055 m1A Human chr19 + 3721752 3721752 3721752 GGAAGAGGGGCAGGTGCAGCCGGGAGCTGCGGAGCTGGAGGGAGGAGGACGAGAGCCCGGCCCTC GGAAGAGGGGCAGGTGCAGCCGGGAGCTGCGGCGCTGGAGGGAGGAGGACGAGAGCCCGGCCCTC A C TJP3 Ensembl:ENSG00000105289 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3721727..3721869 26863196 MeRIP-seq:(Medium) rs1041817779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582877 80930 RMVar_ID_80930 Human_SNP_ID_656204870 m1A Human chr19 - 3751555 3751555 3751555 CAGCTGAGTGAGGCCAACGGCCCCCGCCCCACAGGAGACGAAGTCGCAGACGTCGGTGACACTCA CAGCTGAGTGAGGCCAACGGCCCCCGCCCCACGGGAGACGAAGTCGCAGACGTCGGTGACACTCA T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3751405..3751555 32194978 MeRIP-seq:(Medium) rs1217689204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374373,RMVar_hsa_circ_191402 80931 RMVar_ID_80931 Human_SNP_ID_656207832 m1A Human chr19 + 3759720 3759720 3759720 CCTGGGCACCAGCGGGTGGCTCTTCAGGTGTGACTAGAGGCACCGTCTCCAGCCAGGGTTCCGGG CCTGGGCACCAGCGGGTGGCTCTTCAGGTGTGTCTAGAGGCACCGTCTCCAGCCAGGGTTCCGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3759670..3759820 32194978 MeRIP-seq:(Medium) rs1349184888 Functional Loss SNV dbSNP153 33..33 33 - - - 80932 RMVar_ID_80932 Human_SNP_ID_656208015 m1A Human chr19 + 3760073 3760073 3760073 GATGGGCCCACCAGATCGCCTGGCAGAGCTTCAAACTGCTGCACCAGCTCCTGAAGGCTTGACTC GATGGGCCCACCAGATCGCCTGGCAGAGCTTCGAACTGCTGCACCAGCTCCTGAAGGCTTGACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3760022..3760141 26863196 MeRIP-seq:(Medium) rs1443089103 Functional Loss SNV dbSNP153 33..33 33 - - - 80933 RMVar_ID_80933 Human_SNP_ID_656208911 m1A Human chr19 + 3762734 3762734 3762734 TGGCGACCAAACGCCTTTTCGGGGCTACCCGGACGTGGGCCGGCTGGGGGGCCTGGGAGCTCCTA TGGCGACCAAACGCCTTTTCGGGGCTACCCGGTCGTGGGCCGGCTGGGGGGCCTGGGAGCTCCTA A T MRPL54 Ensembl:ENSG00000183617 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3762676..3765275 26863196 MeRIP-seq:(Medium) rs1427227803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4524256,Human_RBP_ID_5115993,Human_RBP_ID_22448164 Human_Splice_Rec_1938323,Human_Splice_Rec_1938327 80934 RMVar_ID_80934 Human_SNP_ID_656208913 m1A Human chr19 - 3762746 3762737 3762747 AGTGGCGGGGTTTAGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTCCGGGTAGCCCCGAAAAGGC AGTGGCGGGGTTTAGGAGCTCCCAGGCCCCC__________ACGTCCGGGTAGCCCCGAAAAGGC TGGGCCGGCTG T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3762701..3762807 26863196 MeRIP-seq:(Medium) rs752748377 Functional Loss DEL dbSNP153 32..41 33 - - - 80935 RMVar_ID_80935 Human_SNP_ID_656208934 m1A Human chr19 - 3762765 3762765 3762765 GGGCCAGGAGTCTTCCGGAAGTGGCGGGGTTTAGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTC GGGCCAGGAGTCTTCCGGAAGTGGCGGGGTTTGGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3762687..3762833 26863410 MeRIP-seq:(Medium) rs756424817 Functional Loss SNV dbSNP153 33..33 33 - - - 80936 RMVar_ID_80936 Human_SNP_ID_656210429 m1A Human chr19 + 3767323 3767323 3767323 GACCCTGGAGGAGCTGGACCCCGAGAGCCGGGAGTACTGGCGGCGGCTGCGGAAACAGAACATCT GACCCTGGAGGAGCTGGACCCCGAGAGCCGGGCGTACTGGCGGCGGCTGCGGAAACAGAACATCT A C MRPL54 Ensembl:ENSG00000183617 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:3767273..3767500 32194978 MeRIP-seq:(Medium) rs747654364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773221,Human_RBP_ID_22446319,Human_RBP_ID_22762678,Human_RBP_ID_23795312 Human_Splice_Rec_1938326 80937 RMVar_ID_80937 Human_SNP_ID_656269070 m1A Human chr19 - 3958648 3958648 3958649 GTGGGACGGGGAGGGTGGGATGGACGGCGGACAGGCAGTCCCCACGCTGCTGGGTGGCGCCGGGC GTGGGACGGGGAGGGTGGGATGGACGGCGGAACGGCAGTCCCCACGCTGCTGGGTGGCGCCGGGC TG GT DAPK3 Ensembl:ENSG00000167657 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3958451..3959478 26863196 MeRIP-seq:(Medium) rs71339086 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_54423,Human_RBP_ID_771928,Human_RBP_ID_825563,Human_RBP_ID_4526798,Human_RBP_ID_5144941,Human_RBP_ID_8197401,Human_RBP_ID_8233571,Human_RBP_ID_17670274,Human_RBP_ID_26471796,Human_RBP_ID_27815824 Human_miRNA_ID_2225784,Human_miRNA_ID_2726551,Human_miRNA_ID_2757115 RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 80938 RMVar_ID_80938 Human_SNP_ID_656271707 m1A Human chr19 + 3964982 3964973 3964983 GTGCCCTTCTGCCGGCACTTCCGCACGATCGCAAACTGGCCGCTGGAGGAGGGGGAGGGAGTGAG GTGCCCTTCTGCCGGCACTTCCGC__________ACTGGCCGCTGGAGGAGGGGGAGGGAGTGAG CACGATCGCAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3964674..3965020;chr19:3964626..3965032 26863196 MeRIP-seq:(Medium) rs1568193027 Functional Loss DEL dbSNP153 25..34 33 - - - 80939 RMVar_ID_80939 Human_SNP_ID_656271720 m1A Human chr19 - 3964986 3964979 3964986 CCCACTCACTCCCTCCCCCTCCTCCAGCGGCCAGTTTGCGATCGTGCGGAAGTGCCGGCAGAAGG CCCACTCACTCCCTCCCCCTCCTCCAGCGGCC_______GATCGTGCGGAAGTGCCGGCAGAAGG CGCAAACT C DAPK3 Ensembl:ENSG00000167657 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3964939..3969857 26863196 MeRIP-seq:(Medium) rs757496722 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_3954199,Human_RBP_ID_18994071,Human_RBP_ID_26785044 Human_Splice_Rec_1938772,Human_Splice_Rec_1938786,Human_Splice_Rec_1938808,Human_Splice_Rec_1938814,Human_Splice_Rec_1938818 RMVar_hsa_circ_41242,RMVar_hsa_circ_16480,RMVar_hsa_circ_191422,RMVar_hsa_circ_77341,RMVar_hsa_circ_310796,RMVar_hsa_circ_191427 80940 RMVar_ID_80940 Human_SNP_ID_656272340 m1A Human chr19 + 3966970 3966970 3966970 GCCGGGAAAGAAACTCCCCAAGAGCTGAGCCCACCCTCTTCGCTTCTCTGTAACTTCCCCAGCCC GCCGGGAAAGAAACTCCCCAAGAGCTGAGCCCGCCCTCTTCGCTTCTCTGTAACTTCCCCAGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3966967..3967056 26863196 MeRIP-seq:(Medium) rs1466669592 Functional Loss SNV dbSNP153 33..33 33 - - - 80941 RMVar_ID_80941 Human_SNP_ID_656273401 m1A Human chr19 + 3970542 3970540 3970543 CTCCCTCCAATTCTGAATTTTCCAAGAACCGGACGACGCCTTCCACGCTCCTGAAAGCCCACTTT CTCCCTCCAATTCTGAATTTTCCAAGAACCG___GACGCCTTCCACGCTCCTGAAAGCCCACTTT GGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3970537..3970624 26863196 MeRIP-seq:(Medium) rs1429751856 Functional Loss DEL dbSNP153 32..34 33 - - - 80942 RMVar_ID_80942 Human_SNP_ID_656273599 m1A Human chr19 - 3971060 3971060 3971060 GCGCGGGGCTTCTGGAGGCGGCGGCGGTGGCCAGCGCGGCGGCGCCGGCCGTATTCTCCGGGCTG GCGCGGGGCTTCTGGAGGCGGCGGCGGTGGCCGGCGCGGCGGCGCCGGCCGTATTCTCCGGGCTG T C DAPK3 Ensembl:ENSG00000167657 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3970580..3971136 26863196 MeRIP-seq:(Medium) rs1429865808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557099,Human_RBP_ID_9381675,Human_RBP_ID_18421191 Human_Splice_Rec_1938805 80943 RMVar_ID_80943 Human_SNP_ID_656275540 m1A Human chr19 - 3976392 3976392 3976392 CGCTGCGTGCCATCACTCAACCATAACACTTGATGCCGTTTCTTTCAATATTTATTTCCAGAGTC CGCTGCGTGCCATCACTCAACCATAACACTTGGTGCCGTTTCTTTCAATATTTATTTCCAGAGTC T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3976342..3976681 26863196 MeRIP-seq:(Medium) rs1286430367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521415,Human_RBP_ID_1015816,Human_RBP_ID_1239969,Human_RBP_ID_1294238,Human_RBP_ID_1373256,Human_RBP_ID_1564569,Human_RBP_ID_1887294,Human_RBP_ID_2565336,Human_RBP_ID_3571491,Human_RBP_ID_5585674,Human_RBP_ID_6760934,Human_RBP_ID_8097332,Human_RBP_ID_8486964,Human_RBP_ID_8833689,Human_RBP_ID_9087792,Human_RBP_ID_9258716,Human_RBP_ID_9292144,Human_RBP_ID_17268936,Human_RBP_ID_17384022,Human_RBP_ID_17499873,Human_RBP_ID_17695616,Human_RBP_ID_17924329,Human_RBP_ID_18732089,Human_RBP_ID_20349386,Human_RBP_ID_22422507,Human_RBP_ID_22502756,Human_RBP_ID_22972223,Human_RBP_ID_23177948,Human_RBP_ID_23278390,Human_RBP_ID_23796789,Human_RBP_ID_26653684,Human_RBP_ID_27273949,Human_RBP_ID_27473481,Human_RBP_ID_27679740 Human_miRNA_ID_196772,Human_miRNA_ID_697446,Human_miRNA_ID_702380 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_96281,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_113274,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191441,RMVar_hsa_circ_191442,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_191428 80944 RMVar_ID_80944 Human_SNP_ID_656275574 m1A Human chr19 - 3976481 3976481 3976481 GCACCCACAGCACCACGTCCTCGAATTCTCAGACGACACCTGGAGACTGTCCCGACACAGCGACG GCACCCACAGCACCACGTCCTCGAATTCTCAGGCGACACCTGGAGACTGTCCCGACACAGCGACG T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs527408761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54428,Human_RBP_ID_521417,Human_RBP_ID_1015816,Human_RBP_ID_1373258,Human_RBP_ID_1564569,Human_RBP_ID_1887294,Human_RBP_ID_3571491,Human_RBP_ID_4526988,Human_RBP_ID_6760942,Human_RBP_ID_8486965,Human_RBP_ID_8833694,Human_RBP_ID_9292147,Human_RBP_ID_13452295,Human_RBP_ID_17268936,Human_RBP_ID_17384023,Human_RBP_ID_17499877,Human_RBP_ID_17924332,Human_RBP_ID_18305023,Human_RBP_ID_18441286,Human_RBP_ID_18732089,Human_RBP_ID_22234683,Human_RBP_ID_23796792,Human_RBP_ID_24485475,Human_RBP_ID_26468005,Human_RBP_ID_26989626,Human_RBP_ID_27273949,Human_RBP_ID_27467860 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_96281,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_113274,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191441,RMVar_hsa_circ_191442,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_191428,RMVar_hsa_circ_191444,RMVar_hsa_circ_379036 80945 RMVar_ID_80945 Human_SNP_ID_656275592 m1A Human chr19 - 3976507 3976507 3976507 AGCGCCTGCCGCCCCGGGGACTCGCAGCACCCACAGCACCACGTCCTCGAATTCTCAGACGACAC AGCGCCTGCCGCCCCGGGGACTCGCAGCACCCGCAGCACCACGTCCTCGAATTCTCAGACGACAC T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3976236..3976627 26863196 MeRIP-seq:(Medium) rs1292718712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54428,Human_RBP_ID_521417,Human_RBP_ID_771941,Human_RBP_ID_1015819,Human_RBP_ID_1564570,Human_RBP_ID_1887294,Human_RBP_ID_3571491,Human_RBP_ID_4526992,Human_RBP_ID_6760944,Human_RBP_ID_8256067,Human_RBP_ID_8486965,Human_RBP_ID_8833694,Human_RBP_ID_17268936,Human_RBP_ID_17384023,Human_RBP_ID_17499877,Human_RBP_ID_18191757,Human_RBP_ID_18732090,Human_RBP_ID_22810708,Human_RBP_ID_22972228,Human_RBP_ID_23132030,Human_RBP_ID_24484358,Human_RBP_ID_26468008,Human_RBP_ID_26989626,Human_RBP_ID_27157584,Human_RBP_ID_27273949,Human_RBP_ID_27467865 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_96281,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_113274,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191441,RMVar_hsa_circ_191442,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_191428,RMVar_hsa_circ_191444,RMVar_hsa_circ_379036 80946 RMVar_ID_80946 Human_SNP_ID_656275639 m1A Human chr19 + 3976559 3976559 3976559 GGCGGCAGGCGCTGCAGGAAGGGCCGCCTACAATTTGTCCAGGAAGTTGTCCAGGGCAGGGATGC GGCGGCAGGCGCTGCAGGAAGGGCCGCCTACAGTTTGTCCAGGAAGTTGTCCAGGGCAGGGATGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3976176..3976746 26863410 MeRIP-seq:(Medium) rs1200134597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191445 80947 RMVar_ID_80947 Human_SNP_ID_656275966 m1A Human chr19 - 3977301 3977301 3977301 GGTCGGTGGCATCTACGGGGTTTTGAACAGGAAGCGGGGCCACGTGTTCGAGGAGTCCCAGGTGG GGTCGGTGGCATCTACGGGGTTTTGAACAGGAGGCGGGGCCACGTGTTCGAGGAGTCCCAGGTGG T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3977215..3977304 26863196 MeRIP-seq:(Medium) rs768383239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54429,Human_RBP_ID_303862,Human_RBP_ID_521433,Human_RBP_ID_771944,Human_RBP_ID_1015827,Human_RBP_ID_1189649,Human_RBP_ID_1564585,Human_RBP_ID_1887301,Human_RBP_ID_3571499,Human_RBP_ID_4526998,Human_RBP_ID_5190660,Human_RBP_ID_6760955,Human_RBP_ID_8256072,Human_RBP_ID_8486974,Human_RBP_ID_8833709,Human_RBP_ID_13452323,Human_RBP_ID_17924341,Human_RBP_ID_18191771,Human_RBP_ID_18732106,Human_RBP_ID_22448166,Human_RBP_ID_22810711,Human_RBP_ID_23131195,Human_RBP_ID_23796799,Human_RBP_ID_26989634,Human_RBP_ID_27157588,Human_RBP_ID_27273962 Human_Splice_Rec_1938844,Human_Splice_Rec_1938845 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_96281,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191441,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_300030,RMVar_hsa_circ_370612,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191449,RMVar_hsa_circ_84758,RMVar_hsa_circ_191450,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446 80948 RMVar_ID_80948 Human_SNP_ID_656276087 m1A Human chr19 - 3977503 3977503 3977503 CACCGCGGAGGGGGCCAGATCATCCCCACAGCACGGCGCTGCCTCTATGCCAGTGTGCTGACCGC CACCGCGGAGGGGGCCAGATCATCCCCACAGCGCGGCGCTGCCTCTATGCCAGTGTGCTGACCGC T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3977197..3977630 26863196 MeRIP-seq:(Medium) rs117017020 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_521437,Human_RBP_ID_771946,Human_RBP_ID_1015832,Human_RBP_ID_1564594,Human_RBP_ID_3571501,Human_RBP_ID_4527006,Human_RBP_ID_6760958,Human_RBP_ID_8486979,Human_RBP_ID_8833715,Human_RBP_ID_13452329,Human_RBP_ID_17695621,Human_RBP_ID_18191780,Human_RBP_ID_18732111,Human_RBP_ID_22810715,Human_RBP_ID_26989637,Human_RBP_ID_27273964,Human_RBP_ID_27467877 Human_Splice_Rec_1938843 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_370612,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191449,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_281483,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452 80949 RMVar_ID_80949 Human_SNP_ID_656276095 m1A Human chr19 - 3977527 3977527 3977527 GTCACCCTGCACGCCGACGCCATCCACCGCGGAGGGGGCCAGATCATCCCCACAGCACGGCGCTG GTCACCCTGCACGCCGACGCCATCCACCGCGGGGGGGGCCAGATCATCCCCACAGCACGGCGCTG T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3977218..3977650 26863410 MeRIP-seq:(Medium) rs1384715544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54430,Human_RBP_ID_240540,Human_RBP_ID_521440,Human_RBP_ID_1564595,Human_RBP_ID_4527006,Human_RBP_ID_8256073,Human_RBP_ID_8833717,Human_RBP_ID_9087798,Human_RBP_ID_18191781,Human_RBP_ID_18732111,Human_RBP_ID_22810715,Human_RBP_ID_26989637,Human_RBP_ID_27273964,Human_RBP_ID_27467877 Human_Splice_Rec_1938842,Human_Splice_Rec_1938843 Human_miRNA_ID_2726552 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_370612,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191449,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_281483,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452 80950 RMVar_ID_80950 Human_SNP_ID_656276973 m1A Human chr19 - 3979242 3979242 3979242 GCTTTAAAGCTGAGCTGAGCTAGGCTCTGCAGACGCCTAGACTTGATCTCGGTCTTGGTCTCAGC GCTTTAAAGCTGAGCTGAGCTAGGCTCTGCAGGCGCCTAGACTTGATCTCGGTCTTGGTCTCAGC T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3979237..3979490 26863196 MeRIP-seq:(Medium) rs1378673938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1564628,Human_RBP_ID_13452407,Human_RBP_ID_25415158 RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_119387,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_91044,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191459,RMVar_hsa_circ_191460,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456 80951 RMVar_ID_80951 Human_SNP_ID_656277019 m1A Human chr19 - 3979331 3979331 3979331 ACCTGGAGGAGGACCACGCCTGCATCCCCATCAAGGTGAGGCGCCAGTGACCAGCCTTCCCCACG ACCTGGAGGAGGACCACGCCTGCATCCCCATCGAGGTGAGGCGCCAGTGACCAGCCTTCCCCACG T C EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3979326..3979400 26863196 MeRIP-seq:(Medium) rs1347917447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521466,Human_RBP_ID_1015840,Human_RBP_ID_1189655,Human_RBP_ID_1239970,Human_RBP_ID_1294250,Human_RBP_ID_1564630,Human_RBP_ID_1887320,Human_RBP_ID_3571515,Human_RBP_ID_4527019,Human_RBP_ID_6760991,Human_RBP_ID_8097343,Human_RBP_ID_8487000,Human_RBP_ID_8833732,Human_RBP_ID_9292167,Human_RBP_ID_13452427,Human_RBP_ID_17268961,Human_RBP_ID_17384030,Human_RBP_ID_17924359,Human_RBP_ID_18192752,Human_RBP_ID_18441292,Human_RBP_ID_18532456,Human_RBP_ID_18732145,Human_RBP_ID_20389802,Human_RBP_ID_22502769,Human_RBP_ID_22810728,Human_RBP_ID_22979244,Human_RBP_ID_26474930,Human_RBP_ID_26989658,Human_RBP_ID_27157598,Human_RBP_ID_27273972,Human_RBP_ID_27467895,Human_RBP_ID_27679745 Human_Splice_Rec_1938839,Human_Splice_Rec_1938847 RMVar_hsa_circ_9801,RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_119387,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_91044,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191459,RMVar_hsa_circ_191460,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_333123,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_41563,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_6864,RMVar_hsa_circ_191463,RMVar_hsa_circ_191461 80952 RMVar_ID_80952 Human_SNP_ID_656277231 m1A Human chr19 + 3979742 3979742 3979742 CCAATCCACCAACCACAGCAACCCACACAGCCACAACTCAGGACACAAGCCGTCCCCCCTCAGGG CCAATCCACCAACCACAGCAACCCACACAGCCGCAACTCAGGACACAAGCCGTCCCCCCTCAGGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3979740..3980059 26863196 MeRIP-seq:(Medium) rs1167358403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191465 80953 RMVar_ID_80953 Human_SNP_ID_656277247 m1A Human chr19 + 3979771 3979771 3979771 GCCACAACTCAGGACACAAGCCGTCCCCCCTCAGGGTGTCTGCTCCCAGCAGGTGCACTCCGTGC GCCACAACTCAGGACACAAGCCGTCCCCCCTCGGGGTGTCTGCTCCCAGCAGGTGCACTCCGTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3979768..3980016 26863196 MeRIP-seq:(Medium) rs1317008888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191465 80954 RMVar_ID_80954 Human_SNP_ID_656277527 m1A Human chr19 + 3980478 3980478 3980478 CCCAAGACTTGGAGCAGGGCAGGGCCCGCAACAGTGCCAAGGGGCCTGCACATCACCCAGCTGCT CCCAAGACTTGGAGCAGGGCAGGGCCCGCAACGGTGCCAAGGGGCCTGCACATCACCCAGCTGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3980473..3980622 26863196 MeRIP-seq:(Medium) rs371755070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191470 80955 RMVar_ID_80955 Human_SNP_ID_656277528 m1A Human chr19 + 3980478 3980478 3980478 CCCAAGACTTGGAGCAGGGCAGGGCCCGCAACAGTGCCAAGGGGCCTGCACATCACCCAGCTGCT CCCAAGACTTGGAGCAGGGCAGGGCCCGCAACTGTGCCAAGGGGCCTGCACATCACCCAGCTGCT A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3980473..3980622 26863196 MeRIP-seq:(Medium) rs371755070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191470 80956 RMVar_ID_80956 Human_SNP_ID_656277754 m1A Human chr19 - 3980950 3980950 3980950 CAGGCTGTGATGCGCCGCTGGCTGCCTGCCGGAGACGCCTTGTTGCAGATGATCACCATCCACCT CAGGCTGTGATGCGCCGCTGGCTGCCTGCCGGCGACGCCTTGTTGCAGATGATCACCATCCACCT T G EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3980926..3980950 32194978 MeRIP-seq:(Medium) rs1256678774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54435,Human_RBP_ID_521506,Human_RBP_ID_913702,Human_RBP_ID_1015858,Human_RBP_ID_1564657,Human_RBP_ID_1887335,Human_RBP_ID_4568203,Human_RBP_ID_5190674,Human_RBP_ID_8487025,Human_RBP_ID_8833789,Human_RBP_ID_9087816,Human_RBP_ID_9292191,Human_RBP_ID_17268978,Human_RBP_ID_17386606,Human_RBP_ID_17924394,Human_RBP_ID_18191807,Human_RBP_ID_18732182,Human_RBP_ID_22533077,Human_RBP_ID_23131217,Human_RBP_ID_23796863 Human_Splice_Rec_1938832,Human_Splice_Rec_1938854,Human_Splice_Rec_1938860 RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191435,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_119387,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_91044,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191459,RMVar_hsa_circ_191460,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_333123,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_41563,RMVar_hsa_circ_103939,RMVar_hsa_circ_114037,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_191461,RMVar_hsa_circ_371516,RMVar_hsa_circ_191467,RMVar_hsa_circ_77228,RMVar_hsa_circ_91448,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_126724,RMVar_hsa_circ_191466,RMVar_hsa_circ_375271,RMVar_hsa_circ_108591,RMVar_hsa_circ_191473,RMVar_hsa_circ_191475,RMVar_hsa_circ_191477,RMVar_hsa_circ_89037,RMVar_hsa_circ_191476,RMVar_hsa_circ_191474,RMVar_hsa_circ_30907,RMVar_hsa_circ_269798 80957 RMVar_ID_80957 Human_SNP_ID_656278008 m1A Human chr19 - 3981423 3981423 3981423 TAGGTGTTTGATGCGATCATGAATTTCAAGAAAGAGGAGACAGCAAAACTGATAGAGAAACTGGA TAGGTGTTTGATGCGATCATGAATTTCAAGAAGGAGGAGACAGCAAAACTGATAGAGAAACTGGA T C EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3981344..3981490 26863410 MeRIP-seq:(Medium) rs776322385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521515,Human_RBP_ID_1015860,Human_RBP_ID_1564668,Human_RBP_ID_1887337,Human_RBP_ID_3571535,Human_RBP_ID_4568214,Human_RBP_ID_6761030,Human_RBP_ID_8487035,Human_RBP_ID_8833796,Human_RBP_ID_9087817,Human_RBP_ID_13452481,Human_RBP_ID_17268979,Human_RBP_ID_17499910,Human_RBP_ID_18305039,Human_RBP_ID_18732186,Human_RBP_ID_22071486,Human_RBP_ID_22234766,Human_RBP_ID_22502787,Human_RBP_ID_22972290,Human_RBP_ID_23131219,Human_RBP_ID_23177974,Human_RBP_ID_23796925,Human_RBP_ID_25415196,Human_RBP_ID_26989694,Human_RBP_ID_27679756 Human_Splice_Rec_1938830,Human_Splice_Rec_1938831,Human_Splice_Rec_1938852,Human_Splice_Rec_1938853,Human_Splice_Rec_1938858,Human_Splice_Rec_1938859 RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_91044,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191459,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_41563,RMVar_hsa_circ_103939,RMVar_hsa_circ_114037,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_191467,RMVar_hsa_circ_77228,RMVar_hsa_circ_91448,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_126724,RMVar_hsa_circ_108591,RMVar_hsa_circ_191475,RMVar_hsa_circ_191477,RMVar_hsa_circ_89037,RMVar_hsa_circ_191476,RMVar_hsa_circ_191474,RMVar_hsa_circ_30907,RMVar_hsa_circ_191478,RMVar_hsa_circ_346740,RMVar_hsa_circ_374276 80958 RMVar_ID_80958 Human_SNP_ID_656278297 m1A Human chr19 - 3981928 3981928 3981928 ACCCCATCTTCAAGGTGAGTGAGGGCTGCGCCAGGCACCCCGCCGATGCGACTATTGGCCCTCGG ACCCCATCTTCAAGGTGAGTGAGGGCTGCGCCTGGCACCCCGCCGATGCGACTATTGGCCCTCGG T A EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3981926..3982025 26863196 MeRIP-seq:(Medium) rs1568201479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913704,Human_RBP_ID_5372839,Human_RBP_ID_18996033,Human_RBP_ID_19088706,Human_RBP_ID_22476393,Human_RBP_ID_26785052 RMVar_hsa_circ_101398,RMVar_hsa_circ_116544,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_103939,RMVar_hsa_circ_114037,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_191467,RMVar_hsa_circ_77228,RMVar_hsa_circ_91448,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_126724,RMVar_hsa_circ_108591,RMVar_hsa_circ_191475,RMVar_hsa_circ_191477,RMVar_hsa_circ_191476,RMVar_hsa_circ_191478,RMVar_hsa_circ_374276 80959 RMVar_ID_80959 Human_SNP_ID_656278315 m1A Human chr19 + 3981963 3981963 3981963 CGCAGCCCTCACTCACCTTGAAGATGGGGTCCAGGATCAGCTGGCAGAAGGTGCGTGGCAGCTTC CGCAGCCCTCACTCACCTTGAAGATGGGGTCCGGGATCAGCTGGCAGAAGGTGCGTGGCAGCTTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3981951..3982000 26863196 MeRIP-seq:(Medium) rs1204833430 Functional Loss SNV dbSNP153 33..33 33 - - - 80960 RMVar_ID_80960 Human_SNP_ID_656278351 m1A Human chr19 - 3982035 3982035 3982035 GCCTCTCCTTGCCAGGTACTTTGACCCAGCCAACGGCAAGTTCAGCAAGTCAGCCACCAGCCCCG GCCTCTCCTTGCCAGGTACTTTGACCCAGCCACCGGCAAGTTCAGCAAGTCAGCCACCAGCCCCG T G EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3981927..3982073 26863196 MeRIP-seq:(Medium) rs1260504687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54437,Human_RBP_ID_521520,Human_RBP_ID_913705,Human_RBP_ID_1015862,Human_RBP_ID_1564683,Human_RBP_ID_1887342,Human_RBP_ID_3571539,Human_RBP_ID_4527193,Human_RBP_ID_5190676,Human_RBP_ID_8487038,Human_RBP_ID_8833799,Human_RBP_ID_9292196,Human_RBP_ID_18191813,Human_RBP_ID_18441302,Human_RBP_ID_18732194,Human_RBP_ID_22234776,Human_RBP_ID_22533078,Human_RBP_ID_26816651,Human_RBP_ID_26989700 Human_Splice_Rec_1938828,Human_Splice_Rec_1938829,Human_Splice_Rec_1938850,Human_Splice_Rec_1938851,Human_Splice_Rec_1938856,Human_Splice_Rec_1938857 RMVar_hsa_circ_101398,RMVar_hsa_circ_116544,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_103939,RMVar_hsa_circ_114037,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_191467,RMVar_hsa_circ_77228,RMVar_hsa_circ_91448,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_126724,RMVar_hsa_circ_108591,RMVar_hsa_circ_38110,RMVar_hsa_circ_191475,RMVar_hsa_circ_191477,RMVar_hsa_circ_191476,RMVar_hsa_circ_191478,RMVar_hsa_circ_374276,RMVar_hsa_circ_344028,RMVar_hsa_circ_191479 80961 RMVar_ID_80961 Human_SNP_ID_656278446 m1A Human chr19 + 3982207 3982205 3982208 CACCACGCCCCTACGTCGCTGCCACTACCCCCAGGTGTCAGGAATCCCCCACCATATCCCGCGGG CACCACGCCCCTACGTCGCTGCCACTACCCC___GTGTCAGGAATCCCCCACCATATCCCGCGGG CCAG C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3982200..3982450 26863410 MeRIP-seq:(Medium) rs756534077 Functional Loss DEL dbSNP153 32..34 33 - - - 80962 RMVar_ID_80962 Human_SNP_ID_656278448 m1A Human chr19 + 3982207 3982206 3982207 CACCACGCCCCTACGTCGCTGCCACTACCCCCAGGTGTCAGGAATCCCCCACCATATCCCGCGGG CACCACGCCCCTACGTCGCTGCCACTACCCCC_GGTGTCAGGAATCCCCCACCATATCCCGCGGG CA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3982200..3982450 26863410 MeRIP-seq:(Medium) rs780405319 Functional Loss DEL dbSNP153 33..33 33 - - - 80963 RMVar_ID_80963 Human_SNP_ID_656278449 m1A Human chr19 + 3982207 3982207 3982207 CACCACGCCCCTACGTCGCTGCCACTACCCCCAGGTGTCAGGAATCCCCCACCATATCCCGCGGG CACCACGCCCCTACGTCGCTGCCACTACCCCCGGGTGTCAGGAATCCCCCACCATATCCCGCGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3982200..3982450 26863410 MeRIP-seq:(Medium) rs1164068897 Functional Loss SNV dbSNP153 33..33 33 - - - 80964 RMVar_ID_80964 Human_SNP_ID_656279026 m1A Human chr19 - 3983150 3983150 3983150 GACTTCTCCTCGGAGGTGACTGCTGCCCTCCGAGTCACCGATGGCGCATTGGTGGTGGTGGACTG GACTTCTCCTCGGAGGTGACTGCTGCCCTCCGTGTCACCGATGGCGCATTGGTGGTGGTGGACTG T A EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3983011..3983149 26863196 MeRIP-seq:(Medium) rs1312620268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54442,Human_RBP_ID_521534,Human_RBP_ID_1564705,Human_RBP_ID_1887354,Human_RBP_ID_4527213,Human_RBP_ID_5190680,Human_RBP_ID_5443089,Human_RBP_ID_6761062,Human_RBP_ID_8487058,Human_RBP_ID_8833821,Human_RBP_ID_9087828,Human_RBP_ID_17268993,Human_RBP_ID_17384048,Human_RBP_ID_17499924,Human_RBP_ID_17695657,Human_RBP_ID_17924406,Human_RBP_ID_18191833,Human_RBP_ID_18732214,Human_RBP_ID_22533082,Human_RBP_ID_22810769,Human_RBP_ID_23131235,Human_RBP_ID_23177977,Human_RBP_ID_23796949,Human_RBP_ID_26468067,Human_RBP_ID_27157618,Human_RBP_ID_27274049,Human_RBP_ID_27467982 Human_Splice_Rec_1938823 RMVar_hsa_circ_101398,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191446,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_120799,RMVar_hsa_circ_191455,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_103939,RMVar_hsa_circ_114037,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_77228,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_108591,RMVar_hsa_circ_38110,RMVar_hsa_circ_191477,RMVar_hsa_circ_191476,RMVar_hsa_circ_191478,RMVar_hsa_circ_374276,RMVar_hsa_circ_344028,RMVar_hsa_circ_80843,RMVar_hsa_circ_191480,RMVar_hsa_circ_343623,RMVar_hsa_circ_191482,RMVar_hsa_circ_373741,RMVar_hsa_circ_191483,RMVar_hsa_circ_191484,RMVar_hsa_circ_191485 80965 RMVar_ID_80965 Human_SNP_ID_656279066 m1A Human chr19 + 3983225 3983225 3983225 GGGGAGTCAATGAGGTTGATGAGGAAGCCGGCACCGTCCTTGCTCTGCTTGATGAAGTTCAAGTC GGGGAGTCAATGAGGTTGATGAGGAAGCCGGCGCCGTCCTTGCTCTGCTTGATGAAGTTCAAGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3982792..3983334 26863196 MeRIP-seq:(Medium) rs755924592 Functional Loss SNV dbSNP153 33..33 33 - - - 80966 RMVar_ID_80966 Human_SNP_ID_656279536 m1A Human chr19 - 3984313 3984313 3984313 CTTCACGGTAGACCAGATCCGCGCCATCATGGACAAGAAGGCCAACATCCGCAACATGTCTGTCA CTTCACGGTAGACCAGATCCGCGCCATCATGGGCAAGAAGGCCAACATCCGCAACATGTCTGTCA T C EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:3984083..3984388;chr19:3984076..3984375;chr19:3984076..3984380;chr19:3984083..3984391 26863196 MeRIP-seq:(Medium) rs747080912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54444,Human_RBP_ID_280154,Human_RBP_ID_521558,Human_RBP_ID_1015882,Human_RBP_ID_1564728,Human_RBP_ID_1887379,Human_RBP_ID_3571566,Human_RBP_ID_4527255,Human_RBP_ID_5468768,Human_RBP_ID_5585694,Human_RBP_ID_6761196,Human_RBP_ID_8487086,Human_RBP_ID_8833836,Human_RBP_ID_9087837,Human_RBP_ID_13452869,Human_RBP_ID_17269002,Human_RBP_ID_17384056,Human_RBP_ID_17499932,Human_RBP_ID_18441311,Human_RBP_ID_18532468,Human_RBP_ID_18732245,Human_RBP_ID_22502804,Human_RBP_ID_22533084,Human_RBP_ID_22810781,Human_RBP_ID_22972362,Human_RBP_ID_26474939,Human_RBP_ID_27274059,Human_RBP_ID_27467993 Human_Splice_Rec_1938820,Human_Splice_Rec_1938862,Human_Splice_Rec_1938866 RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_191429,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_191446,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_114037,RMVar_hsa_circ_191464,RMVar_hsa_circ_191469,RMVar_hsa_circ_108591,RMVar_hsa_circ_38110,RMVar_hsa_circ_191477,RMVar_hsa_circ_80843,RMVar_hsa_circ_191480,RMVar_hsa_circ_191484,RMVar_hsa_circ_191486,RMVar_hsa_circ_372994 80967 RMVar_ID_80967 Human_SNP_ID_656280115 m1A Human chr19 + 3985332 3985332 3985332 GCGTCCCAGGCTAGGCAGCGTAGGCCCCGCGGAGGCCCCGCCGCCGCTCCGGGGCACCAGCGAGG GCGTCCCAGGCTAGGCAGCGTAGGCCCCGCGGGGGCCCCGCCGCCGCTCCGGGGCACCAGCGAGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3985325..3985475 26863410 MeRIP-seq:(Medium) rs746921933 Functional Loss SNV dbSNP153 33..33 33 - - - 80968 RMVar_ID_80968 Human_SNP_ID_656280124 m1A Human chr19 - 3985347 3985347 3985347 TGGTGAGTAACCCTGCCTCGCTGGTGCCCCGGAGCGGCGGCGGGGCCTCCGCGGGGCCTACGCTG TGGTGAGTAACCCTGCCTCGCTGGTGCCCCGGGGCGGCGGCGGGGCCTCCGCGGGGCCTACGCTG T C EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3985337..3985475 26863410 MeRIP-seq:(Medium) rs1309951116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22358783 RMVar_hsa_circ_93217,RMVar_hsa_circ_191428,RMVar_hsa_circ_123266,RMVar_hsa_circ_114037,RMVar_hsa_circ_191464,RMVar_hsa_circ_191469,RMVar_hsa_circ_108591,RMVar_hsa_circ_191477,RMVar_hsa_circ_191486,RMVar_hsa_circ_372994 80969 RMVar_ID_80969 Human_SNP_ID_656280164 m1A Human chr19 - 3985401 3985401 3985401 CGCGACTCGCTTCTTTCGGTTCTACCTGGGAGAATCCACCGCCATCCGCCACCATGGTGAGTAAC CGCGACTCGCTTCTTTCGGTTCTACCTGGGAGTATCCACCGCCATCCGCCACCATGGTGAGTAAC T A EEF2 Ensembl:ENSG00000167658 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:3985362..3985447 26863410 MeRIP-seq:(Medium) rs201347619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521566,Human_RBP_ID_1189694,Human_RBP_ID_1294272,Human_RBP_ID_1564754,Human_RBP_ID_1887402,Human_RBP_ID_3571580,Human_RBP_ID_4557921,Human_RBP_ID_5421522,Human_RBP_ID_5443093,Human_RBP_ID_5468772,Human_RBP_ID_5499562,Human_RBP_ID_6761320,Human_RBP_ID_8487106,Human_RBP_ID_8833847,Human_RBP_ID_9087841,Human_RBP_ID_9292220,Human_RBP_ID_13453148,Human_RBP_ID_17269006,Human_RBP_ID_17384059,Human_RBP_ID_17499935,Human_RBP_ID_17924433,Human_RBP_ID_18441315,Human_RBP_ID_18732276,Human_RBP_ID_22234837,Human_RBP_ID_22502806,Human_RBP_ID_22533085,Human_RBP_ID_22972399,Human_RBP_ID_26468081,Human_RBP_ID_26989764,Human_RBP_ID_27274068,Human_RBP_ID_27467995,Human_RBP_ID_27679770 Human_Splice_Rec_1938819,Human_Splice_Rec_1938865 RMVar_hsa_circ_93217,RMVar_hsa_circ_191428,RMVar_hsa_circ_123266,RMVar_hsa_circ_114037,RMVar_hsa_circ_191464,RMVar_hsa_circ_191469,RMVar_hsa_circ_108591,RMVar_hsa_circ_191477,RMVar_hsa_circ_191486,RMVar_hsa_circ_372994 80970 RMVar_ID_80970 Human_SNP_ID_656280165 m1A Human chr19 - 3985401 3985401 3985401 CGCGACTCGCTTCTTTCGGTTCTACCTGGGAGAATCCACCGCCATCCGCCACCATGGTGAGTAAC CGCGACTCGCTTCTTTCGGTTCTACCTGGGAGGATCCACCGCCATCCGCCACCATGGTGAGTAAC T C EEF2 Ensembl:ENSG00000167658 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:3985362..3985447 26863410 MeRIP-seq:(Medium) rs201347619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521566,Human_RBP_ID_1189694,Human_RBP_ID_1294272,Human_RBP_ID_1564754,Human_RBP_ID_1887402,Human_RBP_ID_3571580,Human_RBP_ID_4557921,Human_RBP_ID_5421522,Human_RBP_ID_5443093,Human_RBP_ID_5468772,Human_RBP_ID_5499562,Human_RBP_ID_6761320,Human_RBP_ID_8487106,Human_RBP_ID_8833847,Human_RBP_ID_9087841,Human_RBP_ID_9292220,Human_RBP_ID_13453148,Human_RBP_ID_17269006,Human_RBP_ID_17384059,Human_RBP_ID_17499935,Human_RBP_ID_17924433,Human_RBP_ID_18441315,Human_RBP_ID_18732276,Human_RBP_ID_22234837,Human_RBP_ID_22502806,Human_RBP_ID_22533085,Human_RBP_ID_22972399,Human_RBP_ID_26468081,Human_RBP_ID_26989764,Human_RBP_ID_27274068,Human_RBP_ID_27467995,Human_RBP_ID_27679770 Human_Splice_Rec_1938819,Human_Splice_Rec_1938865 RMVar_hsa_circ_93217,RMVar_hsa_circ_191428,RMVar_hsa_circ_123266,RMVar_hsa_circ_114037,RMVar_hsa_circ_191464,RMVar_hsa_circ_191469,RMVar_hsa_circ_108591,RMVar_hsa_circ_191477,RMVar_hsa_circ_191486,RMVar_hsa_circ_372994 80971 RMVar_ID_80971 Human_SNP_ID_656280174 m1A Human chr19 + 3985418 3985410 3985419 CGGATGGCGGTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGAC CGGATGGCGGTGGATTCTCCCAGGT_________AGAAGCGAGTCGCGCCGAGGATGGCGGCGAC TAGAACCGAA T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3985251..3985475 26863196 MeRIP-seq:(Medium) rs773352611 Functional Loss DEL dbSNP153 26..34 33 - - - 80972 RMVar_ID_80972 Human_SNP_ID_656280185 m1A Human chr19 + 3985422 3985422 3985422 TGGCGGTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACG TGGCGGTGGATTCTCCCAGGTAGAACCGAAAGCAGCGAGTCGCGCCGAGGATGGCGGCGACGACG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3985312..3985475 26863196 MeRIP-seq:(Medium) rs765302732 Functional Loss SNV dbSNP153 33..33 33 - - - 80973 RMVar_ID_80973 Human_SNP_ID_656280186 m1A Human chr19 + 3985422 3985422 3985422 TGGCGGTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACG TGGCGGTGGATTCTCCCAGGTAGAACCGAAAGTAGCGAGTCGCGCCGAGGATGGCGGCGACGACG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3985312..3985475 26863196 MeRIP-seq:(Medium) rs765302732 Functional Loss SNV dbSNP153 33..33 33 - - - 80974 RMVar_ID_80974 Human_SNP_ID_656280187 m1A Human chr19 + 3985423 3985423 3985423 GGCGGTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACGG GGCGGTGGATTCTCCCAGGTAGAACCGAAAGACGCGAGTCGCGCCGAGGATGGCGGCGACGACGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3985282..3985475 26863196 MeRIP-seq:(Medium) rs777439048 Functional Loss SNV dbSNP153 33..33 33 - - - 80975 RMVar_ID_80975 Human_SNP_ID_656280188 m1A Human chr19 + 3985423 3985423 3985423 GGCGGTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACGG GGCGGTGGATTCTCCCAGGTAGAACCGAAAGAGGCGAGTCGCGCCGAGGATGGCGGCGACGACGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:3985282..3985475 26863196 MeRIP-seq:(Medium) rs777439048 Functional Loss SNV dbSNP153 33..33 33 - - - 80976 RMVar_ID_80976 Human_SNP_ID_656280197 m1A Human chr19 + 3985427 3985427 3985427 GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACGGCGGA GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGCGTCGCGCCGAGGATGGCGGCGACGACGGCGGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3985314..3985475 26863196 MeRIP-seq:(Medium) rs761180832 Functional Loss SNV dbSNP153 33..33 33 - - - 80977 RMVar_ID_80977 Human_SNP_ID_656280198 m1A Human chr19 + 3985427 3985427 3985427 GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACGGCGGA GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGGGTCGCGCCGAGGATGGCGGCGACGACGGCGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3985314..3985475 26863196 MeRIP-seq:(Medium) rs761180832 Functional Loss SNV dbSNP153 33..33 33 - - - 80978 RMVar_ID_80978 Human_SNP_ID_656280199 m1A Human chr19 + 3985427 3985427 3985427 GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGAGTCGCGCCGAGGATGGCGGCGACGACGGCGGA GTGGATTCTCCCAGGTAGAACCGAAAGAAGCGTGTCGCGCCGAGGATGGCGGCGACGACGGCGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3985314..3985475 26863196 MeRIP-seq:(Medium) rs761180832 Functional Loss SNV dbSNP153 33..33 33 - - - 80979 RMVar_ID_80979 Human_SNP_ID_656288811 m1A Human chr19 - 4012095 4012073 4012095 ATCCTGGGCTCTGTGTGGTGCTAAATACCCACAGCTCACGACAACCAAACACACCTCCACACCCC ATCCTGGGCTCTGTGTGGTGCTAAATACCCAC______________________CTCCACACCCC GGTGTGTTTGGTTGTCGTGAGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4012092..4012185 26863196 MeRIP-seq:(Medium) rs990892288 Functional Loss DEL dbSNP153 33..54 33 - - - 80980 RMVar_ID_80980 Human_SNP_ID_656291066 m1A Human chr19 - 4018805 4018805 4018805 GGCCCTATATTTGTCTTTGTACAAATGTCACCAGAAGGAAAGCCTTCGCTGAGCACCCCATTTAA GGCCCTATATTTGTCTTTGTACAAATGTCACCCGAAGGAAAGCCTTCGCTGAGCACCCCATTTAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4018798..4019156 26863196 MeRIP-seq:(Medium) rs1460010296 Functional Loss SNV dbSNP153 33..33 33 - - - 80981 RMVar_ID_80981 Human_SNP_ID_656297152 m1A Human chr19 + 4035758 4035752 4035758 CCCACACATCCATACAGTCCACACCATCACACACACACACCCACACACATCCATACAGTCCATAC CCCACACATCCATACAGTCCACACCAT______CACACACCCACACACATCCATACAGTCCATAC TCACACA T PIAS4 Ensembl:ENSG00000105229 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4035710..4035862 26863196 MeRIP-seq:(Medium) rs1201731707 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_8111,Human_RBP_ID_139631,Human_RBP_ID_202464,Human_RBP_ID_263114,Human_RBP_ID_1067172,Human_RBP_ID_2573191,Human_RBP_ID_5144947,Human_RBP_ID_5238539,Human_RBP_ID_5469442,Human_RBP_ID_9328377,Human_RBP_ID_9425093,Human_RBP_ID_17655799,Human_RBP_ID_24374448,Human_RBP_ID_24532770,Human_RBP_ID_26759475,Human_RBP_ID_26814985 80982 RMVar_ID_80982 Human_SNP_ID_656297153 m1A Human chr19 + 4035758 4035752 4035758 CCCACACATCCATACAGTCCACACCATCACACACACACACCCACACACATCCATACAGTCCATAC CCCACACATCCATACAGTCCACACCATCA____CACACACCCACACACATCCATACAGTCCATAC TCACACA TCA PIAS4 Ensembl:ENSG00000105229 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4035710..4035862 26863196 MeRIP-seq:(Medium) rs1201731707 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_8111,Human_RBP_ID_139631,Human_RBP_ID_202464,Human_RBP_ID_263114,Human_RBP_ID_1067172,Human_RBP_ID_2573191,Human_RBP_ID_5144947,Human_RBP_ID_5238539,Human_RBP_ID_5469442,Human_RBP_ID_9328377,Human_RBP_ID_9425093,Human_RBP_ID_17655799,Human_RBP_ID_24374448,Human_RBP_ID_24532770,Human_RBP_ID_26759475,Human_RBP_ID_26814985 80983 RMVar_ID_80983 Human_SNP_ID_656297154 m1A Human chr19 + 4035758 4035752 4035758 CCCACACATCCATACAGTCCACACCATCACACACACACACCCACACACATCCATACAGTCCATAC CCCACACATCCATACAGTCCACACCATCACA__CACACACCCACACACATCCATACAGTCCATAC TCACACA TCACA PIAS4 Ensembl:ENSG00000105229 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4035710..4035862 26863196 MeRIP-seq:(Medium) rs1201731707 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8111,Human_RBP_ID_139631,Human_RBP_ID_202464,Human_RBP_ID_263114,Human_RBP_ID_1067172,Human_RBP_ID_2573191,Human_RBP_ID_5144947,Human_RBP_ID_5238539,Human_RBP_ID_5469442,Human_RBP_ID_9328377,Human_RBP_ID_9425093,Human_RBP_ID_17655799,Human_RBP_ID_24374448,Human_RBP_ID_24532770,Human_RBP_ID_26759475,Human_RBP_ID_26814985 80984 RMVar_ID_80984 Human_SNP_ID_656297165 m1A Human chr19 + 4035758 4035758 4035758 CCCACACATCCATACAGTCCACACCATCACACACACACACCCACACACATCCATACAGTCCATAC CCCACACATCCATACAGTCCACACCATCACACCCACACACCCACACACATCCATACAGTCCATAC A C PIAS4 Ensembl:ENSG00000105229 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4035710..4035862 26863196 MeRIP-seq:(Medium) rs1305585567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8111,Human_RBP_ID_139631,Human_RBP_ID_202464,Human_RBP_ID_263114,Human_RBP_ID_1067172,Human_RBP_ID_2573191,Human_RBP_ID_5144947,Human_RBP_ID_5238539,Human_RBP_ID_5469442,Human_RBP_ID_9328377,Human_RBP_ID_9425093,Human_RBP_ID_17655799,Human_RBP_ID_24374448,Human_RBP_ID_24532770,Human_RBP_ID_26759475,Human_RBP_ID_26814985 80985 RMVar_ID_80985 Human_SNP_ID_656297196 m1A Human chr19 + 4035819 4035819 4035819 ATACCATCACACACACCCGCACACATCCATACAGTCCACACCATCACACACACACCCGCACACAT ATACCATCACACACACCCGCACACATCCATACTGTCCACACCATCACACACACACCCGCACACAT A T PIAS4 Ensembl:ENSG00000105229 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4035772..4035885 26863196 MeRIP-seq:(Medium) rs1335983675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7415,Human_RBP_ID_139631,Human_RBP_ID_202466,Human_RBP_ID_263115,Human_RBP_ID_1067173,Human_RBP_ID_2565561,Human_RBP_ID_5088775,Human_RBP_ID_5145602,Human_RBP_ID_5238540,Human_RBP_ID_5369754,Human_RBP_ID_9328378,Human_RBP_ID_9425094,Human_RBP_ID_17655299,Human_RBP_ID_19028748,Human_RBP_ID_22370892,Human_RBP_ID_22533294,Human_RBP_ID_24374448,Human_RBP_ID_24532771,Human_RBP_ID_24552758,Human_RBP_ID_26759476,Human_RBP_ID_26814986 80986 RMVar_ID_80986 Human_SNP_ID_656297795 m1A Human chr19 - 4036625 4036600 4036625 GTGTGTATGACAGTGTGGACTGTATAGATGTGAGACGGTGTGGACTGTATAGATGTGTGTGTGTA GTGTGTATGACAGTGTGGACTGTATAGATGTG_________________________TGTGTGTA ACACATCTATACAGTCCACACCGTCT A lnc-ZBTB7A-1,lnc-ZBTB7A-1:2,lnc-ZBTB7A-1:3,lnc-ZBTB7A-1:4 RNACentral:URS00008BB60D,RNACentral:URS00008BBB9A,RNACentral:URS00008B3BAE,RNACentral:URS00008B292C lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4036618..4036744 26863196 MeRIP-seq:(Medium) rs1379181372 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_23797498 80987 RMVar_ID_80987 Human_SNP_ID_656297821 m1A Human chr19 - 4036625 4036625 4036625 GTGTGTATGACAGTGTGGACTGTATAGATGTGAGACGGTGTGGACTGTATAGATGTGTGTGTGTA GTGTGTATGACAGTGTGGACTGTATAGATGTGTGACGGTGTGGACTGTATAGATGTGTGTGTGTA T A lnc-ZBTB7A-1,lnc-ZBTB7A-1:2,lnc-ZBTB7A-1:3,lnc-ZBTB7A-1:4 RNACentral:URS00008BB60D,RNACentral:URS00008BBB9A,RNACentral:URS00008B3BAE,RNACentral:URS00008B292C lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4036618..4036744 26863196 MeRIP-seq:(Medium) rs551594798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23797498 80988 RMVar_ID_80988 Human_SNP_ID_656297822 m1A Human chr19 - 4036625 4036625 4036625 GTGTGTATGACAGTGTGGACTGTATAGATGTGAGACGGTGTGGACTGTATAGATGTGTGTGTGTA GTGTGTATGACAGTGTGGACTGTATAGATGTGGGACGGTGTGGACTGTATAGATGTGTGTGTGTA T C lnc-ZBTB7A-1,lnc-ZBTB7A-1:2,lnc-ZBTB7A-1:3,lnc-ZBTB7A-1:4 RNACentral:URS00008BB60D,RNACentral:URS00008BBB9A,RNACentral:URS00008B3BAE,RNACentral:URS00008B292C lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4036618..4036744 26863196 MeRIP-seq:(Medium) rs551594798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23797498 80989 RMVar_ID_80989 Human_SNP_ID_656300778 m1A Human chr19 + 4043706 4043689 4043706 GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCACCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC GGCGAGGGATGGGGGT_________________CCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC TCTCCCTGGCCCCCTCCA T HSALNG0123335 RNACentral:URS0000E98386 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4043696..4043825 26863196 MeRIP-seq:(Medium) rs1318246167 Functional Loss DEL dbSNP153 17..33 33 - - - 80990 RMVar_ID_80990 Human_SNP_ID_656300789 m1A Human chr19 + 4043706 4043702 4043706 GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCACCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC GGCGAGGGATGGGGGTCTCCCTGGCCCCC____CCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC CTCCA C HSALNG0123335 RNACentral:URS0000E98386 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4043696..4043825 26863196 MeRIP-seq:(Medium) rs1568226440 Functional Loss DEL dbSNP153 30..33 33 - - - 80991 RMVar_ID_80991 Human_SNP_ID_656300794 m1A Human chr19 + 4043706 4043706 4043706 GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCACCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCCCCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC A C HSALNG0123335 RNACentral:URS0000E98386 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4043696..4043825 26863196 MeRIP-seq:(Medium) rs866300187 Functional Loss SNV dbSNP153 33..33 33 - - - 80992 RMVar_ID_80992 Human_SNP_ID_656301343 m1A Human chr19 - 4044979 4044978 4044979 CCTCTGCATGGGCCCAGAGCCGGGACCCCCCCAGCCCAGCCCCGCCCTCCCCAGACTCCGCGCAA CCTCTGCATGGGCCCAGAGCCGGGACCCCCCCCCCCCAGCCCCGCCCTCCCCAGACTCCGCGCAA CT GG ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4044968..4045165 26863196 MeRIP-seq:(Medium) rs1555691475 Functional Loss MNV dbSNP153 33..34 33 - - - Human_RBP_ID_26785059 Human_miRNA_ID_1158126 80993 RMVar_ID_80993 Human_SNP_ID_656301344 m1A Human chr19 - 4044979 4044979 4044979 CCTCTGCATGGGCCCAGAGCCGGGACCCCCCCAGCCCAGCCCCGCCCTCCCCAGACTCCGCGCAA CCTCTGCATGGGCCCAGAGCCGGGACCCCCCCCGCCCAGCCCCGCCCTCCCCAGACTCCGCGCAA T G ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4044968..4045165 26863196 MeRIP-seq:(Medium) rs1180959822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26785059 Human_miRNA_ID_1158126 80994 RMVar_ID_80994 Human_SNP_ID_656301360 m1A Human chr19 + 4045041 4045041 4045041 AGGCTGTGGCCCCCAGGACGGGCGGGTAGTTAAGGCAAAGTGGGCGGGCAGGACAGGCGAAGCTG AGGCTGTGGCCCCCAGGACGGGCGGGTAGTTACGGCAAAGTGGGCGGGCAGGACAGGCGAAGCTG A C HSALNG0123335 RNACentral:URS0000E98386 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4044992..4045097 26863196 MeRIP-seq:(Medium) rs1363037802 Functional Loss SNV dbSNP153 33..33 33 - - - 80995 RMVar_ID_80995 Human_SNP_ID_656301854 m1A Human chr19 + 4046502 4046497 4046502 AAGTTGGTTGTAACTTGTAAACATGTTTTTAAATTAAGAATTAAGATAAAGTGTAGTACCCGTTC AAGTTGGTTGTAACTTGTAAACATGTTT_____TTAAGAATTAAGATAAAGTGTAGTACCCGTTC TTTAAA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4046404..4046504 32194978 MeRIP-seq:(Medium) rs1421784451 Functional Loss DEL dbSNP153 29..33 33 - - - 80996 RMVar_ID_80996 Human_SNP_ID_656301881 m1A Human chr19 - 4046591 4046586 4046591 AACTAGAAAAAAAAAAGGTTTTACAAAATGAAAGGAAGGAAAAAAAAAAAGGCAACCAACCACAT AACTAGAAAAAAAAAAGGTTTTACAAAATGAA_____GGAAAAAAAAAAAGGCAACCAACCACAT CTTCCT C ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4046589..4046672 26863196 MeRIP-seq:(Medium) rs975671474 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 80997 RMVar_ID_80997 Human_SNP_ID_656302088 m1A Human chr19 - 4047161 4047161 4047161 ACTAAGGGAGGGGTCTCCCTCTCCATCTCCCCAGTGGCCTCCCCGCCTCCAACCCTGCCTGCGGC ACTAAGGGAGGGGTCTCCCTCTCCATCTCCCCCGTGGCCTCCCCGCCTCCAACCCTGCCTGCGGC T G ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4047110..4047245 26863196 MeRIP-seq:(Medium) rs866873177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772149,Human_RBP_ID_8197415,Human_RBP_ID_17081588,Human_RBP_ID_17567503,Human_RBP_ID_18944816,Human_RBP_ID_24484403 Human_miRNA_ID_842933,Human_miRNA_ID_2147309,Human_miRNA_ID_2294473,Human_miRNA_ID_2368188,Human_miRNA_ID_2988736,Human_miRNA_ID_3015972,Human_miRNA_ID_3022435 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 80998 RMVar_ID_80998 Human_SNP_ID_656302339 m1A Human chr19 + 4047841 4047841 4047841 GTCACCTCCTCCACCGGCGCCCGCTACATTCAACCGGCCCAAGCCGTCGGGGCTGGCCACGTCCT GTCACCTCCTCCACCGGCGCCCGCTACATTCAGCCGGCCCAAGCCGTCGGGGCTGGCCACGTCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4047797..4048197 32194978 MeRIP-seq:(Medium) rs267605424 Functional Loss SNV dbSNP153 33..33 33 - - - 80999 RMVar_ID_80999 Human_SNP_ID_656304593 m1A Human chr19 + 4054142 4054142 4054142 TCTTCTCCACCTTCTGCGACCAGGCCGGGTAGACGTCGCCGTCGTGGGCGCCGCTGAAGTACTTC TCTTCTCCACCTTCTGCGACCAGGCCGGGTAGCCGTCGCCGTCGTGGGCGCCGCTGAAGTACTTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4054141..4054330 26863196 MeRIP-seq:(Medium) rs752781965 Functional Loss SNV dbSNP153 33..33 33 - - - 81000 RMVar_ID_81000 Human_SNP_ID_656305079 m1A Human chr19 + 4055246 4055246 4055246 CGTCCACGCCGCCGGCCATCTTCCGCGCCGAGACCTGCAGCAGTGGGGAAGGAGAGGGCGCTCGT CGTCCACGCCGCCGGCCATCTTCCGCGCCGAGGCCTGCAGCAGTGGGGAAGGAGAGGGCGCTCGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4055216..4065674 26863196 MeRIP-seq:(Medium) rs1313735557 Functional Loss SNV dbSNP153 33..33 33 - - - 81001 RMVar_ID_81001 Human_SNP_ID_656308186 m1A Human chr19 + 4065100 4065100 4065100 GGTAGGGAGCGGGAGGGAGGGGGCTGGATCCCACCAGCTCCCCCCTCCCCTGCCCGGGCTCAGGC GGTAGGGAGCGGGAGGGAGGGGGCTGGATCCCGCCAGCTCCCCCCTCCCCTGCCCGGGCTCAGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4065096..4065296 26863196 MeRIP-seq:(Medium) rs377554656 Functional Loss SNV dbSNP153 33..33 33 - - - 81002 RMVar_ID_81002 Human_SNP_ID_656308314 m1A Human chr19 - 4065395 4065395 4065395 AGGAGCCCCCCGCGCGGGCGAGGCGGCGGGGGACCGCGGGCCGGGCGGGGGCCGCGCGCTGCGGC AGGAGCCCCCCGCGCGGGCGAGGCGGCGGGGGGCCGCGGGCCGGGCGGGGGCCGCGCGCTGCGGC T C ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr19:4065392..4065544;chr19:4065386..4065690 26863196 MeRIP-seq:(Medium) rs1005006017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582942,Human_RBP_ID_8195811,Human_RBP_ID_9328395,Human_RBP_ID_18461118,Human_RBP_ID_19091608,Human_RBP_ID_22359508,Human_RBP_ID_22720380,Human_RBP_ID_26759505,Human_RBP_ID_26785090 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 81003 RMVar_ID_81003 Human_SNP_ID_656308342 m1A Human chr19 - 4065477 4065468 4065477 CGGAGGGAGCCAGCCCAGCCGCAGCCGCCGCCACCGCCGCCGCCGGGGCCGGGCCCCCTCGCCGC CGGAGGGAGCCAGCCCAGCCGCAGCCGCCGCC_________GCCGGGGCCGGGCCCCCTCGCCGC CGGCGGCGGT C ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4065370..4065570 26863196 MeRIP-seq:(Medium) rs1029409455 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_8195812,Human_RBP_ID_18461745,Human_RBP_ID_26785091 Human_Splice_Rec_1938917 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 81004 RMVar_ID_81004 Human_SNP_ID_656308844 m1A Human chr19 - 4066674 4066672 4066674 GCGCGCCCCGGCCCGGCCCCGCGAGGTAAGTCAGCGCCCGGCGCGGCCCCCGGCACGGGGTGCAG GCGCGCCCCGGCCCGGCCCCGCGAGGTAAGTC__CGCCCGGCGCGGCCCCCGGCACGGGGTGCAG GCT G ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4066658..4066823 26863196 MeRIP-seq:(Medium) rs1199745620 Functional Loss DEL dbSNP153 33..34 33 - - - 81005 RMVar_ID_81005 Human_SNP_ID_656308845 m1A Human chr19 - 4066674 4066674 4066674 GCGCGCCCCGGCCCGGCCCCGCGAGGTAAGTCAGCGCCCGGCGCGGCCCCCGGCACGGGGTGCAG GCGCGCCCCGGCCCGGCCCCGCGAGGTAAGTCCGCGCCCGGCGCGGCCCCCGGCACGGGGTGCAG T G ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4066658..4066823 26863196 MeRIP-seq:(Medium) rs919628699 Functional Loss SNV dbSNP153 33..33 33 - - - 81006 RMVar_ID_81006 Human_SNP_ID_656313490 m1A Human chr19 - 4081759 4081757 4081760 AGGAGAAGGGGGAGTAGGAGGGAGGAAGGAGGAGCAGAGAAGAGCAGGGAGGAGGGAGGAGAGGC AGGAGAAGGGGGAGTAGGAGGGAGGAAGGAG___CAGAGAAGAGCAGGGAGGAGGGAGGAGAGGC GCTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4081747..4082383 26863196 MeRIP-seq:(Medium) rs1008255230 Functional Loss DEL dbSNP153 32..34 33 - - - 81007 RMVar_ID_81007 Human_SNP_ID_656316285 m1A Human chr19 - 4090619 4090619 4090619 TGTAAAACCCTGCGGCTGAACCAGCCCGGCACACCCACGCGCACCGCCGTGTGACAGTGGCCGGG TGTAAAACCCTGCGGCTGAACCAGCCCGGCACGCCCACGCGCACCGCCGTGTGACAGTGGCCGGG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:4090532..4090629 26863410 MeRIP-seq:(Medium) rs375253105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18191845 Human_Splice_Rec_1938942,Human_Splice_Rec_1938948,Human_Splice_Rec_1938962,Human_Splice_Rec_1938982,Human_Splice_Rec_1938990,Human_Splice_Rec_1938998 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 81008 RMVar_ID_81008 Human_SNP_ID_656318297 m1A Human chr19 + 4097237 4097233 4097237 TAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAGAAAGAAAAGGAAAAGAAAAGCCAAAAGGCATCA TAAAAAAAAAAAAAAAAAAAAAAAGAAAG____AAGAAAAGGAAAAGAAAAGCCAAAAGGCATCA GAAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4097235..4097309 26863196 MeRIP-seq:(Medium) rs758313763 Functional Loss DEL dbSNP153 30..33 33 - - - 81009 RMVar_ID_81009 Human_SNP_ID_656318300 m1A Human chr19 + 4097237 4097237 4097237 TAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAGAAAGAAAAGGAAAAGAAAAGCCAAAAGGCATCA TAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAGGAAGAAAAGGAAAAGAAAAGCCAAAAGGCATCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4097235..4097309 26863196 MeRIP-seq:(Medium) rs776265329 Functional Loss SNV dbSNP153 33..33 33 - - - 81010 RMVar_ID_81010 Human_SNP_ID_656318328 m1A Human chr19 - 4097290 4097288 4097290 CTGCCATGGCCATCTTTGAACTCCTGGACTATATTGTGAACGAGGTTTGTGCTTGATGCCTTTTG CTGCCATGGCCATCTTTGAACTCCTGGACTAT__TGTGAACGAGGTTTGTGCTTGATGCCTTTTG AAT A MAP2K2 Ensembl:ENSG00000126934 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:4097276..4097350;chr19:4097276..4097300 26863196 MeRIP-seq:(Medium) rs770978109 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1888239,Human_RBP_ID_5190697,Human_RBP_ID_13458937,Human_RBP_ID_18733288,Human_RBP_ID_22973104,Human_RBP_ID_25418162 Human_Splice_Rec_1938936,Human_Splice_Rec_1938937,Human_Splice_Rec_1938944,Human_Splice_Rec_1938945,Human_Splice_Rec_1938956,Human_Splice_Rec_1938957,Human_Splice_Rec_1938976,Human_Splice_Rec_1938977,Human_Splice_Rec_1938992,Human_Splice_Rec_1938993,Human_Splice_Rec_1939000,Human_Splice_Rec_1939001 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 81011 RMVar_ID_81011 Human_SNP_ID_656318328 m1A Human chr19 + 4097289 4097288 4097290 CCAAAAGGCATCAAGCACAAACCTCGTTCACAATATAGTCCAGGAGTTCAAAGATGGCCATGGCA CCAAAAGGCATCAAGCACAAACCTCGTTCACA__ATAGTCCAGGAGTTCAAAGATGGCCATGGCA AAT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4097276..4097325 26863196 MeRIP-seq:(Medium) rs770978109 Functional Loss DEL dbSNP153 33..34 33 - - - 81012 RMVar_ID_81012 Human_SNP_ID_656318329 m1A Human chr19 - 4097290 4097290 4097290 CTGCCATGGCCATCTTTGAACTCCTGGACTATATTGTGAACGAGGTTTGTGCTTGATGCCTTTTG CTGCCATGGCCATCTTTGAACTCCTGGACTATGTTGTGAACGAGGTTTGTGCTTGATGCCTTTTG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:4097276..4097350;chr19:4097276..4097300 26863196 MeRIP-seq:(Medium) rs775489626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1888239,Human_RBP_ID_5190697,Human_RBP_ID_13458937,Human_RBP_ID_18733288,Human_RBP_ID_22973104,Human_RBP_ID_25418162 Human_Splice_Rec_1938936,Human_Splice_Rec_1938937,Human_Splice_Rec_1938944,Human_Splice_Rec_1938945,Human_Splice_Rec_1938956,Human_Splice_Rec_1938957,Human_Splice_Rec_1938976,Human_Splice_Rec_1938977,Human_Splice_Rec_1938992,Human_Splice_Rec_1938993,Human_Splice_Rec_1939000,Human_Splice_Rec_1939001 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 81013 RMVar_ID_81013 Human_SNP_ID_656318330 m1A Human chr19 - 4097290 4097290 4097290 CTGCCATGGCCATCTTTGAACTCCTGGACTATATTGTGAACGAGGTTTGTGCTTGATGCCTTTTG CTGCCATGGCCATCTTTGAACTCCTGGACTATCTTGTGAACGAGGTTTGTGCTTGATGCCTTTTG T G MAP2K2 Ensembl:ENSG00000126934 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:4097276..4097350;chr19:4097276..4097300 26863196 MeRIP-seq:(Medium) rs775489626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1888239,Human_RBP_ID_5190697,Human_RBP_ID_13458937,Human_RBP_ID_18733288,Human_RBP_ID_22973104,Human_RBP_ID_25418162 Human_Splice_Rec_1938936,Human_Splice_Rec_1938937,Human_Splice_Rec_1938944,Human_Splice_Rec_1938945,Human_Splice_Rec_1938956,Human_Splice_Rec_1938957,Human_Splice_Rec_1938976,Human_Splice_Rec_1938977,Human_Splice_Rec_1938992,Human_Splice_Rec_1938993,Human_Splice_Rec_1939000,Human_Splice_Rec_1939001 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 81014 RMVar_ID_81014 Human_SNP_ID_656318880 m1A Human chr19 - 4099163 4099163 4099163 GCCTGAATCTGCAACTTCCGGTCTGGACGCGCAGTGCCCTGCGCGGGGCCTGCTGTGCCAGGGTC GCCTGAATCTGCAACTTCCGGTCTGGACGCGCGGTGCCCTGCGCGGGGCCTGCTGTGCCAGGGTC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4099162..4099399 26863196 MeRIP-seq:(Medium) rs760344244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 81015 RMVar_ID_81015 Human_SNP_ID_656319775 m1A Human chr19 + 4101268 4101268 4101268 CATGATCTGGTGCTTCTCTCGGAGGTACGCCAAGCCCCGGAGAACCTGCAGGGGAGCGCGGAGGG CATGATCTGGTGCTTCTCTCGGAGGTACGCCATGCCCCGGAGAACCTGCAGGGGAGCGCGGAGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4101084..4101270 32194978 MeRIP-seq:(Medium) rs1057517898 Functional Loss SNV dbSNP153 33..33 33 - - - 81016 RMVar_ID_81016 Human_SNP_ID_656324926 m1A Human chr19 + 4117531 4117530 4117531 TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCGACCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCAGCCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC GA AG - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4117480..4117565 26863196 MeRIP-seq:(Medium) rs1555698682 Functional Loss MNV dbSNP153 32..33 33 - - - Clinvar_Rec_379 81017 RMVar_ID_81017 Human_SNP_ID_656324930 m1A Human chr19 + 4117531 4117531 4117531 TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCGACCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCGCCCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4117480..4117565 26863196 MeRIP-seq:(Medium) rs1135401787 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_380 81018 RMVar_ID_81018 Human_SNP_ID_656324931 m1A Human chr19 + 4117531 4117531 4117531 TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCGACCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC TCCTTTCGAAGTCATCGTCTTTGAGTTCGCCGGCCTTGGCTTTCTGGGTGAGAAAGGCTTCCAGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4117480..4117565 26863196 MeRIP-seq:(Medium) rs1135401787 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_380 81019 RMVar_ID_81019 Human_SNP_ID_656326858 m1A Human chr19 - 4124078 4124078 4124078 GGCTGCGGCGTCAGCCTTCTTCGGGCCTCGGCAGCGGTAGCGGCTCGCTCGCCTCAGCCCCAGCG GGCTGCGGCGTCAGCCTTCTTCGGGCCTCGGCCGCGGTAGCGGCTCGCTCGCCTCAGCCCCAGCG T G MAP2K2 Ensembl:ENSG00000126934 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:4123978..4124129 26863410 MeRIP-seq:(Medium) rs1430476686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240093,Human_RBP_ID_771356,Human_RBP_ID_826399,Human_RBP_ID_4530549,Human_RBP_ID_5421551,Human_RBP_ID_5443121,Human_RBP_ID_5499615,Human_RBP_ID_18191853,Human_RBP_ID_22502974 81020 RMVar_ID_81020 Human_SNP_ID_656342504 m1A Human chr19 - 4174945 4174945 4174945 CCCACGCCTGACCCGTCCCGCCCCTCGGCAGGACCGCCATGCTGACCTCCGCATCCATGGCTACG CCCACGCCTGACCCGTCCCGCCCCTCGGCAGGGCCGCCATGCTGACCTCCGCATCCATGGCTACG T C SIRT6 Ensembl:ENSG00000077463 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4174825..4174966 26863196 MeRIP-seq:(Medium) rs1397744469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1939124,Human_Splice_Rec_1939136,Human_Splice_Rec_1939148,Human_Splice_Rec_1939162,Human_Splice_Rec_1939174,Human_Splice_Rec_1939188,Human_Splice_Rec_1939196,Human_Splice_Rec_1939208,Human_Splice_Rec_1939220,Human_Splice_Rec_1939230,Human_Splice_Rec_1939248 81021 RMVar_ID_81021 Human_SNP_ID_656342578 m1A Human chr19 - 4175067 4175066 4175067 GGGAACCTGCCGCTGGCTACCAAGCGCCGGGGAGGCCGCCTGGTCATCGTCAACCTGCAGCCCAC GGGAACCTGCCGCTGGCTACCAAGCGCCGGGG_GGCCGCCTGGTCATCGTCAACCTGCAGCCCAC CT C SIRT6 Ensembl:ENSG00000077463 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4174705..4175204 32194978 MeRIP-seq:(Medium) rs1214638184 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18996046 Human_Splice_Rec_1939122,Human_Splice_Rec_1939123,Human_Splice_Rec_1939134,Human_Splice_Rec_1939135,Human_Splice_Rec_1939146,Human_Splice_Rec_1939147,Human_Splice_Rec_1939160,Human_Splice_Rec_1939161,Human_Splice_Rec_1939172,Human_Splice_Rec_1939173,Human_Splice_Rec_1939186,Human_Splice_Rec_1939187,Human_Splice_Rec_1939195,Human_Splice_Rec_1939206,Human_Splice_Rec_1939207,Human_Splice_Rec_1939218,Human_Splice_Rec_1939219,Human_Splice_Rec_1939229,Human_Splice_Rec_1939240,Human_Splice_Rec_1939247 RMVar_hsa_circ_126347,RMVar_hsa_circ_191498 81022 RMVar_ID_81022 Human_SNP_ID_656342579 m1A Human chr19 - 4175067 4175067 4175067 GGGAACCTGCCGCTGGCTACCAAGCGCCGGGGAGGCCGCCTGGTCATCGTCAACCTGCAGCCCAC GGGAACCTGCCGCTGGCTACCAAGCGCCGGGGGGGCCGCCTGGTCATCGTCAACCTGCAGCCCAC T C SIRT6 Ensembl:ENSG00000077463 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4174705..4175204 32194978 MeRIP-seq:(Medium) rs1363534581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18996046 Human_Splice_Rec_1939122,Human_Splice_Rec_1939123,Human_Splice_Rec_1939134,Human_Splice_Rec_1939135,Human_Splice_Rec_1939146,Human_Splice_Rec_1939147,Human_Splice_Rec_1939160,Human_Splice_Rec_1939161,Human_Splice_Rec_1939172,Human_Splice_Rec_1939173,Human_Splice_Rec_1939186,Human_Splice_Rec_1939187,Human_Splice_Rec_1939195,Human_Splice_Rec_1939206,Human_Splice_Rec_1939207,Human_Splice_Rec_1939218,Human_Splice_Rec_1939219,Human_Splice_Rec_1939229,Human_Splice_Rec_1939240,Human_Splice_Rec_1939247 RMVar_hsa_circ_126347,RMVar_hsa_circ_191498 81023 RMVar_ID_81023 Human_SNP_ID_656342850 m1A Human chr19 - 4175750 4175750 4175750 CTCCTCAGCTTCCTCATTGCAGGGGAGAGCTGAGGGACACCATCCTAGACTGGGAGGACTCCCTG CTCCTCAGCTTCCTCATTGCAGGGGAGAGCTGCGGGACACCATCCTAGACTGGGAGGACTCCCTG T G SIRT6 Ensembl:ENSG00000077463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr19:4175662..4175827;chr19:4175700..4179155 26863196,32194978 MeRIP-seq:(Medium) rs144978048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241124,Human_RBP_ID_1016316,Human_RBP_ID_23257682 Human_Splice_Rec_1939132,Human_Splice_Rec_1939133,Human_Splice_Rec_1939158,Human_Splice_Rec_1939159,Human_Splice_Rec_1939170,Human_Splice_Rec_1939171,Human_Splice_Rec_1939184,Human_Splice_Rec_1939185,Human_Splice_Rec_1939204,Human_Splice_Rec_1939205,Human_Splice_Rec_1939217,Human_Splice_Rec_1939228,Human_Splice_Rec_1939238,Human_Splice_Rec_1939239,Human_Splice_Rec_1939258 RMVar_hsa_circ_16728 81024 RMVar_ID_81024 Human_SNP_ID_656344386 m1A Human chr19 - 4180893 4180893 4180893 CTCTCTCCCCCCACAGATCTTCGACCCCCCGGAGGAGCTGGAGCGGAAGGTGTGGGAACTGGCGA CTCTCTCCCCCCACAGATCTTCGACCCCCCGGTGGAGCTGGAGCGGAAGGTGTGGGAACTGGCGA T A SIRT6 Ensembl:ENSG00000077463 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4180847..4180948;chr19:4180849..4180943;chr19:4180741..4180957 26863196 MeRIP-seq:(Medium) rs199878780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824552,Human_RBP_ID_18994081,Human_RBP_ID_22977591 Human_Splice_Rec_1939126,Human_Splice_Rec_1939138,Human_Splice_Rec_1939150,Human_Splice_Rec_1939176,Human_Splice_Rec_1939198,Human_Splice_Rec_1939210,Human_Splice_Rec_1939232,Human_Splice_Rec_1939242,Human_Splice_Rec_1939250,Human_Splice_Rec_1939264 81025 RMVar_ID_81025 Human_SNP_ID_656366677 m1A Human chr19 - 4251139 4251139 4251139 CTTGAAGGTGATCTCTGCCAGGCAGCGCGTGCACTTGATGTAAAAGCGGAAGATGGGCAGGCCCA CTTGAAGGTGATCTCTGCCAGGCAGCGCGTGCCCTTGATGTAAAAGCGGAAGATGGGCAGGCCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr19:4251088..4251227;chr19:4249291..4258318 26863196,32194978 MeRIP-seq:(Medium) rs1165364062 Functional Loss SNV dbSNP153 33..33 33 - - - 81026 RMVar_ID_81026 Human_SNP_ID_656368750 m1A Human chr19 - 4258196 4258196 4258196 GGCGGCGGGGCTGAGTGCATGGGGATCGCACCACGGGGCAAACCCTGTCTGGCCTCGGGGGCCAC GGCGGCGGGGCTGAGTGCATGGGGATCGCACCGCGGGGCAAACCCTGTCTGGCCTCGGGGGCCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4258194..4258487 26863196 MeRIP-seq:(Medium) rs1165821741 Functional Loss SNV dbSNP153 33..33 33 - - - 81027 RMVar_ID_81027 Human_SNP_ID_656369969 m1A Human chr19 - 4261949 4261949 4261949 AGATGGGAACTTGGACGTGCTCTGTTTGGGGAACAGTGCCTGGGATGTACCTGCTGGGGTGGCGA AGATGGGAACTTGGACGTGCTCTGTTTGGGGAGCAGTGCCTGGGATGTACCTGCTGGGGTGGCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4261947..4262054 26863196 MeRIP-seq:(Medium) rs201152988 Functional Loss SNV dbSNP153 33..33 33 - - - 81028 RMVar_ID_81028 Human_SNP_ID_656371636 m1A Human chr19 + 4267479 4267479 4267479 CTTGAGTGCCAAGCCTAGGGCAGTGGGGAGCCATAGAGGAGTTTAGAGCAGAGGAGGAATGTGGT CTTGAGTGCCAAGCCTAGGGCAGTGGGGAGCCGTAGAGGAGTTTAGAGCAGAGGAGGAATGTGGT A G YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4267477..4267616 26863196 MeRIP-seq:(Medium) rs117184884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112665,RMVar_hsa_circ_114032,RMVar_hsa_circ_191509,RMVar_hsa_circ_76601,RMVar_hsa_circ_191510,RMVar_hsa_circ_191511 81029 RMVar_ID_81029 Human_SNP_ID_656383691 m1A Human chr19 - 4304650 4304650 4304650 CTTTGCCGCGGCCGGTAGCCAATGGCCCGCCGAGCCCTCGCCGCCGCCGCGCCCCCGGTTAGCGC CTTTGCCGCGGCCGGTAGCCAATGGCCCGCCGGGCCCTCGCCGCCGCCGCGCCCCCGGTTAGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4304643..4304769 26863196 MeRIP-seq:(Medium) rs886950948 Functional Loss SNV dbSNP153 33..33 33 - - - 81030 RMVar_ID_81030 Human_SNP_ID_656383692 m1A Human chr19 - 4304650 4304650 4304650 CTTTGCCGCGGCCGGTAGCCAATGGCCCGCCGAGCCCTCGCCGCCGCCGCGCCCCCGGTTAGCGC CTTTGCCGCGGCCGGTAGCCAATGGCCCGCCGCGCCCTCGCCGCCGCCGCGCCCCCGGTTAGCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4304643..4304769 26863196 MeRIP-seq:(Medium) rs886950948 Functional Loss SNV dbSNP153 33..33 33 - - - 81031 RMVar_ID_81031 Human_SNP_ID_656384150 m1A Human chr19 - 4305895 4305895 4305895 GGACACACACAGGTGCACACACACATGTGCGCACACAGGTACACACACGTGTACGCACATGTACA GGACACACACAGGTGCACACACACATGTGCGCCCACAGGTACACACACGTGTACGCACATGTACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4305892..4306025 26863196 MeRIP-seq:(Medium) rs766984864 Functional Loss SNV dbSNP153 33..33 33 - - - 81032 RMVar_ID_81032 Human_SNP_ID_656396210 m1A Human chr19 + 4343675 4343675 4343675 GCAGGGGCGCGGGGCTGCAGAGCCGTGGGGCGAGCGGCCTCCCTGCAGCCTCTCGCTGTCCGCAG GCAGGGGCGCGGGGCTGCAGAGCCGTGGGGCGCGCGGCCTCCCTGCAGCCTCTCGCTGTCCGCAG A C MPND Ensembl:ENSG00000008382 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:4343669..4343796 26863196 MeRIP-seq:(Medium) rs1334070252 Functional Loss SNV dbSNP153 33..33 33 - - - 81033 RMVar_ID_81033 Human_SNP_ID_656396256 m1A Human chr19 + 4343792 4343792 4343792 GGACGAGGACGAAGCGGAGGCCGAGGACCCTGAGCGGCCGAATGCGGGAGCGGGCGGTGGACGCA GGACGAGGACGAAGCGGAGGCCGAGGACCCTGCGCGGCCGAATGCGGGAGCGGGCGGTGGACGCA A C MPND Ensembl:ENSG00000008382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4343558..4344000 26863196 MeRIP-seq:(Medium) rs962124605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18994085 Human_Splice_Rec_1939792,Human_Splice_Rec_1939814,Human_Splice_Rec_1939834,Human_Splice_Rec_1939858 81034 RMVar_ID_81034 Human_SNP_ID_656402512 m1A Human chr19 - 4361596 4361596 4361596 TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCACCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCGCCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC T C SH3GL1 Ensembl:ENSG00000141985 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4361226..4361812;chr19:4361426..4362622 26863196 MeRIP-seq:(Medium) rs552613793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240380,Human_RBP_ID_522932,Human_RBP_ID_17387166,Human_RBP_ID_22069530 Human_miRNA_ID_2147318,Human_miRNA_ID_2387343,Human_miRNA_ID_2388816,Human_miRNA_ID_2988744,Human_miRNA_ID_3022444,Human_miRNA_ID_3066344 RMVar_hsa_circ_92594,RMVar_hsa_circ_106560,RMVar_hsa_circ_99436,RMVar_hsa_circ_191525,RMVar_hsa_circ_191527,RMVar_hsa_circ_78251,RMVar_hsa_circ_191526,RMVar_hsa_circ_191524 81035 RMVar_ID_81035 Human_SNP_ID_656402513 m1A Human chr19 - 4361596 4361596 4361596 TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCACCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCCCCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC T G SH3GL1 Ensembl:ENSG00000141985 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4361226..4361812;chr19:4361426..4362622 26863196 MeRIP-seq:(Medium) rs552613793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240380,Human_RBP_ID_522932,Human_RBP_ID_17387166,Human_RBP_ID_22069530 Human_miRNA_ID_2147318,Human_miRNA_ID_2387343,Human_miRNA_ID_2388816,Human_miRNA_ID_2988744,Human_miRNA_ID_3022444,Human_miRNA_ID_3066344 RMVar_hsa_circ_92594,RMVar_hsa_circ_106560,RMVar_hsa_circ_99436,RMVar_hsa_circ_191525,RMVar_hsa_circ_191527,RMVar_hsa_circ_78251,RMVar_hsa_circ_191526,RMVar_hsa_circ_191524 81036 RMVar_ID_81036 Human_SNP_ID_656402869 m1A Human chr19 + 4362380 4362378 4362381 CCGGATGGGCTTGTCGGAAGATCGGAAAGACGATGAAGCTAAACACAAGCAAAACGAGGAGGCTG CCGGATGGGCTTGTCGGAAGATCGGAAAGAC___GAAGCTAAACACAAGCAAAACGAGGAGGCTG CGAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4362326..4362400 26863196 MeRIP-seq:(Medium) rs1392283821 Functional Loss DEL dbSNP153 32..34 33 - - - 81037 RMVar_ID_81037 Human_SNP_ID_656403050 m1A Human chr19 - 4362727 4362727 4362727 CACTCACGCCTCTCCCTTCACAGGATGCGGGAAGCTTCCTCACGCCCTAAGCGGGAGTATAAGCC CACTCACGCCTCTCCCTTCACAGGATGCGGGATGCTTCCTCACGCCCTAAGCGGGAGTATAAGCC T A SH3GL1 Ensembl:ENSG00000141985 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4362676..4366993 32194978 MeRIP-seq:(Medium) rs1360789872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1294706,Human_RBP_ID_1373576,Human_RBP_ID_3955993,Human_RBP_ID_22664558 Human_Splice_Rec_1939946,Human_Splice_Rec_1939964,Human_Splice_Rec_1939980 RMVar_hsa_circ_92594,RMVar_hsa_circ_106560,RMVar_hsa_circ_191525,RMVar_hsa_circ_78251,RMVar_hsa_circ_191526,RMVar_hsa_circ_361248,RMVar_hsa_circ_191524 81038 RMVar_ID_81038 Human_SNP_ID_656404859 m1A Human chr19 + 4366933 4366933 4366933 ACAGAGCACGCAGTTTCTTCCTCACCTTCTCCATCTCTTTGAAGTCATCATCCAGCTTGGTCCCC ACAGAGCACGCAGTTTCTTCCTCACCTTCTCCCTCTCTTTGAAGTCATCATCCAGCTTGGTCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4366501..4367032 26863196 MeRIP-seq:(Medium) rs1264123023 Functional Loss SNV dbSNP153 33..33 33 - - - 81039 RMVar_ID_81039 Human_SNP_ID_656404860 m1A Human chr19 + 4366933 4366933 4366933 ACAGAGCACGCAGTTTCTTCCTCACCTTCTCCATCTCTTTGAAGTCATCATCCAGCTTGGTCCCC ACAGAGCACGCAGTTTCTTCCTCACCTTCTCCGTCTCTTTGAAGTCATCATCCAGCTTGGTCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4366501..4367032 26863196 MeRIP-seq:(Medium) rs1264123023 Functional Loss SNV dbSNP153 33..33 33 - - - 81040 RMVar_ID_81040 Human_SNP_ID_656407637 m1A Human chr19 - 4376579 4376577 4376579 AGATGAAGTGTGAAGGGGCAGGCGCACGAGAGAGGAGGCATCAGTGGTGTGTTGGGAGAAGGTGA AGATGAAGTGTGAAGGGGCAGGCGCACGAGAG__GAGGCATCAGTGGTGTGTTGGGAGAAGGTGA CCT C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4376575..4376926 26863196 MeRIP-seq:(Medium) rs1281772227 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5191117,Human_RBP_ID_22593081 RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81041 RMVar_ID_81041 Human_SNP_ID_656407639 m1A Human chr19 - 4376579 4376579 4376579 AGATGAAGTGTGAAGGGGCAGGCGCACGAGAGAGGAGGCATCAGTGGTGTGTTGGGAGAAGGTGA AGATGAAGTGTGAAGGGGCAGGCGCACGAGAGGGGAGGCATCAGTGGTGTGTTGGGAGAAGGTGA T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4376575..4376926 26863196 MeRIP-seq:(Medium) rs1204210185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191117,Human_RBP_ID_22593081 RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81042 RMVar_ID_81042 Human_SNP_ID_656408976 m1A Human chr19 - 4381102 4381102 4381102 GGGGATAGAGAGAGGCAGGGGGACAGAGGCAAAGGGGACAGAGAGAGGGGACAGAGAGAGGCAGG GGGGATAGAGAGAGGCAGGGGGACAGAGGCAAGGGGGACAGAGAGAGGGGACAGAGAGAGGCAGG T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:4381099..4381618;chr19:4381099..4381617 26863196 MeRIP-seq:(Medium) rs1167464881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81043 RMVar_ID_81043 Human_SNP_ID_656409000 m1A Human chr19 - 4381140 4381138 4381140 GAGTCAGGGGAGACAGAGGCAGGGGAACAGAGAGGCAGGGGGATAGAGAGAGGCAGGGGGACAGA GAGTCAGGGGAGACAGAGGCAGGGGAACAGAG__GCAGGGGGATAGAGAGAGGCAGGGGGACAGA CCT C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4381113..4381313 26863196 MeRIP-seq:(Medium) rs374706239 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81044 RMVar_ID_81044 Human_SNP_ID_656409169 m1A Human chr19 - 4381508 4381508 4381508 GACAGAGAAGCAGGGGGACAGAGAGGCGGGGGAGACAGAGGCAGGAGAACGGAGAGAGGCAGAGG GACAGAGAAGCAGGGGGACAGAGAGGCGGGGGTGACAGAGGCAGGAGAACGGAGAGAGGCAGAGG T A SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4381421..4381550 26863196 MeRIP-seq:(Medium) rs895587166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81045 RMVar_ID_81045 Human_SNP_ID_656409170 m1A Human chr19 - 4381508 4381508 4381508 GACAGAGAAGCAGGGGGACAGAGAGGCGGGGGAGACAGAGGCAGGAGAACGGAGAGAGGCAGAGG GACAGAGAAGCAGGGGGACAGAGAGGCGGGGGGGACAGAGGCAGGAGAACGGAGAGAGGCAGAGG T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4381421..4381550 26863196 MeRIP-seq:(Medium) rs895587166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81046 RMVar_ID_81046 Human_SNP_ID_656414037 m1A Human chr19 - 4398289 4398289 4398289 TTGTGTAGATAGAGTCCACCGAGGAATGAGCAATGATCTTAGCAAATGCTTGGGCCAAGGTGGCA TTGTGTAGATAGAGTCCACCGAGGAATGAGCAGTGATCTTAGCAAATGCTTGGGCCAAGGTGGCA T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4398287..4398379 26863196 MeRIP-seq:(Medium) rs1223051681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13466032 RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81047 RMVar_ID_81047 Human_SNP_ID_656414688 m1A Human chr19 - 4400460 4400422 4400461 GAGCTGGCAAGCGGGTGGCGGAGGCGGCGCCGACGGGGACTGCTGAGGCGCGCAGAGGGTCGGCG GAGCTGGCAAGCGGGTGGCGGAGGCGGCGCC__________________________________ GGGCGCCGCCGACCCTCTGCGCGCCTCAGCAGTCCCCGTC G SH3GL1 Ensembl:ENSG00000141985 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:4400364..4400537;chr19:4400124..4400575;chr19:4400125..4400600;chr19:4400154..4400563 26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1463638391 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_240382,Human_RBP_ID_522944,Human_RBP_ID_4533343,Human_RBP_ID_5146125,Human_RBP_ID_9329618,Human_RBP_ID_9353670,Human_RBP_ID_17670276,Human_RBP_ID_22446322,Human_RBP_ID_22977592 RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 81048 RMVar_ID_81048 Human_SNP_ID_656415513 m1A Human chr19 + 4402686 4402686 4402686 GCGGCCGCGGCGGCAGCAGCGGCGCGGGCGGGAGGGCGAAGAGCAGCGGCCGCCTGAGGGGAGCC GCGGCCGCGGCGGCAGCAGCGGCGCGGGCGGGGGGGCGAAGAGCAGCGGCCGCCTGAGGGGAGCC A G CHAF1A Ensembl:ENSG00000167670 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4402651..4402825 26863196 MeRIP-seq:(Medium) rs1195442046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4533367 RMVar_hsa_circ_117327,RMVar_hsa_circ_191530 81049 RMVar_ID_81049 Human_SNP_ID_656417354 m1A Human chr19 + 4408880 4408880 4408880 TGAGTGGTTGTAACTTTAAACGTTCACTAGAGATGGCTTTCTGTCTTTGTTTCAGCCCGTCTGCC TGAGTGGTTGTAACTTTAAACGTTCACTAGAGTTGGCTTTCTGTCTTTGTTTCAGCCCGTCTGCC A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4408877..4409122 26863196 MeRIP-seq:(Medium) rs1278992706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1940042 RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_117327,RMVar_hsa_circ_294806,RMVar_hsa_circ_191530,RMVar_hsa_circ_291666,RMVar_hsa_circ_89465,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_191531 81050 RMVar_ID_81050 Human_SNP_ID_656417508 m1A Human chr19 - 4409304 4409304 4409304 AATGTCTGAAAGGGTCTCTCCAGGAAATGCCAACTTGTCGTTCTGAATGGCCTTCAACAACCCCT AATGTCTGAAAGGGTCTCTCCAGGAAATGCCAGCTTGTCGTTCTGAATGGCCTTCAACAACCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4409254..4409450 26863196 MeRIP-seq:(Medium) rs1172209656 Functional Loss SNV dbSNP153 33..33 33 - - - 81051 RMVar_ID_81051 Human_SNP_ID_656421318 m1A Human chr19 + 4422663 4422661 4422664 AGAGGAGGCCAAGCGGGCCAAGGAGGAGGCCAAGAAGAAGAAGGAGGAAGAGAAGGAGCTTAAGG AGAGGAGGCCAAGCGGGCCAAGGAGGAGGCC___AAGAAGAAGGAGGAAGAGAAGGAGCTTAAGG CAAG C CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4422617..4422800 26863196 MeRIP-seq:(Medium) rs749727242 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_204382,Human_RBP_ID_6768261,Human_RBP_ID_9346653,Human_RBP_ID_22416712,Human_RBP_ID_22664565,Human_RBP_ID_22973754,Human_RBP_ID_24545388,Human_RBP_ID_25446720,Human_RBP_ID_26335210 Human_Splice_Rec_1940018,Human_Splice_Rec_1940046 RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_355383,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_358558,RMVar_hsa_circ_47335,RMVar_hsa_circ_191538 81052 RMVar_ID_81052 Human_SNP_ID_656421335 m1A Human chr19 + 4422726 4422718 4422727 GGAAAAGGAGAGGCGGGAGAAGCGGGAGAAGGATGAGAAGGAGAAGGCGGAGAAGCAGCGGCTCA GGAAAAGGAGAGGCGGGAGAAGCGG_________GAGAAGGAGAAGGCGGAGAAGCAGCGGCTCA GGAGAAGGAT G CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:4422676..4422750 26863196 MeRIP-seq:(Medium) rs769253733 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_8126,Human_RBP_ID_54453,Human_RBP_ID_204383,Human_RBP_ID_826081,Human_RBP_ID_907126,Human_RBP_ID_3956001,Human_RBP_ID_4533963,Human_RBP_ID_17655461,Human_RBP_ID_17934798,Human_RBP_ID_18470403,Human_RBP_ID_18996068,Human_RBP_ID_22069536,Human_RBP_ID_22416712,Human_RBP_ID_22664565,Human_RBP_ID_22741977,Human_RBP_ID_22977593,Human_RBP_ID_23119113,Human_RBP_ID_24374458,Human_RBP_ID_24545389,Human_RBP_ID_24552770,Human_RBP_ID_26335211,Human_RBP_ID_27814918 Human_Splice_Rec_1940019,Human_Splice_Rec_1940047 RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_355383,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_358558,RMVar_hsa_circ_47335,RMVar_hsa_circ_191538 81053 RMVar_ID_81053 Human_SNP_ID_656421499 m1A Human chr19 - 4423329 4423329 4423329 TTTTTCCTTTTTTCCTCAAGTTTAGCCCTGTGAGACAGCAAATGACATTTCAGCCGACTCTTTGC TTTTTCCTTTTTTCCTCAAGTTTAGCCCTGTGGGACAGCAAATGACATTTCAGCCGACTCTTTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4423326..4423400 26863196 MeRIP-seq:(Medium) rs202228370 Functional Loss SNV dbSNP153 33..33 33 - - - 81054 RMVar_ID_81054 Human_SNP_ID_656421627 m1A Human chr19 - 4423764 4423764 4423764 TAAGAGATGGTGATGAGAAAGAGGAGAGGAAGAGGAACAGTATGTGTTGCAAAACATGCAAAGGC TAAGAGATGGTGATGAGAAAGAGGAGAGGAAGGGGAACAGTATGTGTTGCAAAACATGCAAAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4423760..4423911 26863196 MeRIP-seq:(Medium) rs370068913 Functional Loss SNV dbSNP153 33..33 33 - - - 81055 RMVar_ID_81055 Human_SNP_ID_656423077 m1A Human chr19 + 4428625 4428625 4428625 GCTGTGTGCGTCCATGGTGCCTCCTTTCTCCCATTGCTCGAAGACCCCATCGGGTCTCTTCTTGA GCTGTGTGCGTCCATGGTGCCTCCTTTCTCCCGTTGCTCGAAGACCCCATCGGGTCTCTTCTTGA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4428620..4428915 26863196 MeRIP-seq:(Medium) rs1445753230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22661765 RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191534,RMVar_hsa_circ_87365,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_47335,RMVar_hsa_circ_191538,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540 81056 RMVar_ID_81056 Human_SNP_ID_656423443 m1A Human chr19 - 4429761 4429761 4429761 CTTACCCCCTCACTGTGGGACAGGGACTCCCCAGGCTCCTCTTCTTCCCACTCCTCATCACTGTC CTTACCCCCTCACTGTGGGACAGGGACTCCCCCGGCTCCTCTTCTTCCCACTCCTCATCACTGTC T G AC011498.3 Ensembl:ENSG00000267255 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4429631..4429835 26863196 MeRIP-seq:(Medium) rs1467474138 Functional Loss SNV dbSNP153 33..33 33 - - - 81057 RMVar_ID_81057 Human_SNP_ID_656423678 m1A Human chr19 - 4430528 4430528 4430528 GTCATCATCATCCTCAAAAGGAGAAAAAAAAAAGAGTTCATCAGATAGAAAAGCAGAGTGTGTGC GTCATCATCATCCTCAAAAGGAGAAAAAAAAAGGAGTTCATCAGATAGAAAAGCAGAGTGTGTGC T C AC011498.3 Ensembl:ENSG00000267255 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4430526..4430650 26863196 MeRIP-seq:(Medium) rs79536168 Functional Loss SNV dbSNP153 33..33 33 - - - 81058 RMVar_ID_81058 Human_SNP_ID_656424078 m1A Human chr19 + 4431906 4431906 4431906 GGGACTGGTTCCTCAAAAGAGTGCCCGGGCATAGGGGAGCAAGAACCCCAAATAAACTTCTGCTT GGGACTGGTTCCTCAAAAGAGTGCCCGGGCATCGGGGAGCAAGAACCCCAAATAAACTTCTGCTT A C CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4431904..4432225 26863196 MeRIP-seq:(Medium) rs1391859334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17926431 RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191534,RMVar_hsa_circ_87365,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_191538,RMVar_hsa_circ_119539,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540,RMVar_hsa_circ_279390,RMVar_hsa_circ_191541,RMVar_hsa_circ_329098,RMVar_hsa_circ_191542 81059 RMVar_ID_81059 Human_SNP_ID_656424471 m1A Human chr19 + 4433053 4433053 4433053 GATGGGTGGCTCCCCAAGCCTCATGCCCACCCATGTTCCCTCCTGCCAGTCCTGGCCCAGCTGCT GATGGGTGGCTCCCCAAGCCTCATGCCCACCCGTGTTCCCTCCTGCCAGTCCTGGCCCAGCTGCT A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4433051..4433125 26863196 MeRIP-seq:(Medium) rs748879918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19091650 RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191534,RMVar_hsa_circ_87365,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_191538,RMVar_hsa_circ_119539,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540,RMVar_hsa_circ_191541,RMVar_hsa_circ_329098 81060 RMVar_ID_81060 Human_SNP_ID_656427257 m1A Human chr19 + 4442281 4442281 4442281 GTGCTGAAGACATGGACGGCTTCCAGGCAGACACGGAGGAGGAGGAAGAGGAGGAGGGCGACTGT GTGCTGAAGACATGGACGGCTTCCAGGCAGACGCGGAGGAGGAGGAAGAGGAGGAGGGCGACTGT A G CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4433526..4442967 26863196 MeRIP-seq:(Medium) rs766323095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1889056,Human_RBP_ID_4534335,Human_RBP_ID_18996079,Human_RBP_ID_22977989,Human_RBP_ID_23800265 Human_Splice_Rec_1940036,Human_Splice_Rec_1940037,Human_Splice_Rec_1940065 Human_miRNA_ID_2141507,Human_miRNA_ID_2455853,Human_miRNA_ID_2465215 RMVar_hsa_circ_91068,RMVar_hsa_circ_87365,RMVar_hsa_circ_113152,RMVar_hsa_circ_191538,RMVar_hsa_circ_119539,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540,RMVar_hsa_circ_191541,RMVar_hsa_circ_191543 81061 RMVar_ID_81061 Human_SNP_ID_656427280 m1A Human chr19 - 4442313 4442313 4442313 TCACCCGCAGCATCCGGGACATCCACGATCATACAGTCGCCCTCCTCCTCTTCCTCCTCCTCCGT TCACCCGCAGCATCCGGGACATCCACGATCATGCAGTCGCCCTCCTCCTCTTCCTCCTCCTCCGT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4442276..4442447 26863196 MeRIP-seq:(Medium) rs1474771232 Functional Loss SNV dbSNP153 33..33 33 - - - 81062 RMVar_ID_81062 Human_SNP_ID_656428716 m1A Human chr19 + 4446152 4446143 4446153 AAGGCAGCCAGTCGCTCTGCAGGGCCTCCCGGACGAACCCGTACACCGCCCCCAGCCGCTCCCGA AAGGCAGCCAGTCGCTCTGCAGGG__________GAACCCGTACACCGCCCCCAGCCGCTCCCGA GCCTCCCGGAC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4446053..4446200;chr19:4446026..4446200;chr19:4446051..4446219 26863196 MeRIP-seq:(Medium) rs1378120602 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_13469625 RMVar_hsa_circ_191552,RMVar_hsa_circ_98973 81063 RMVar_ID_81063 Human_SNP_ID_656428725 m1A Human chr19 + 4446152 4446152 4446152 AAGGCAGCCAGTCGCTCTGCAGGGCCTCCCGGACGAACCCGTACACCGCCCCCAGCCGCTCCCGA AAGGCAGCCAGTCGCTCTGCAGGGCCTCCCGGGCGAACCCGTACACCGCCCCCAGCCGCTCCCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4446053..4446200;chr19:4446026..4446200;chr19:4446051..4446219 26863196 MeRIP-seq:(Medium) rs774546745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13469625 RMVar_hsa_circ_191552,RMVar_hsa_circ_98973 81064 RMVar_ID_81064 Human_SNP_ID_656428879 m1A Human chr19 + 4446384 4446384 4446384 GCTCCTCCTTCTCCCGCATGGCCTTGGTCCGCAGCACGCTCAGCCGCTCCACCGCCTCGGACCTG GCTCCTCCTTCTCCCGCATGGCCTTGGTCCGCGGCACGCTCAGCCGCTCCACCGCCTCGGACCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4446251..4446429 26863196 MeRIP-seq:(Medium) rs756313078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1567058 RMVar_hsa_circ_191552,RMVar_hsa_circ_98973 81065 RMVar_ID_81065 Human_SNP_ID_656429064 m1A Human chr19 + 4446634 4446634 4446634 TGCCTGTCCAGCTTGGCGCGCACGGGCTCCGCAGCCAGCAGCTGTTCCTTGTGCCTCTCCAGGCT TGCCTGTCCAGCTTGGCGCGCACGGGCTCCGCGGCCAGCAGCTGTTCCTTGTGCCTCTCCAGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4446501..4446725 26863196 MeRIP-seq:(Medium) rs1014995543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191552,RMVar_hsa_circ_98973 81066 RMVar_ID_81066 Human_SNP_ID_656429175 m1A Human chr19 - 4446844 4446844 4446844 CATTGGGTTCCAGAAGGTGTTGCTTCCCGCCCAGGATCAGGGTAAGTGGACAGGGCCTGGCTGAG CATTGGGTTCCAGAAGGTGTTGCTTCCCGCCCCGGATCAGGGTAAGTGGACAGGGCCTGGCTGAG T G UBXN6 Ensembl:ENSG00000167671 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4446826..4446875 26863196 MeRIP-seq:(Medium) rs887523586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771982,Human_RBP_ID_913393,Human_RBP_ID_3954210,Human_RBP_ID_9328412,Human_RBP_ID_23210817,Human_RBP_ID_26335230 Human_Splice_Rec_1940076,Human_Splice_Rec_1940077,Human_Splice_Rec_1940096,Human_Splice_Rec_1940097,Human_Splice_Rec_1940106,Human_Splice_Rec_1940122,Human_Splice_Rec_1940123 RMVar_hsa_circ_105129,RMVar_hsa_circ_114592,RMVar_hsa_circ_191547,RMVar_hsa_circ_80900,RMVar_hsa_circ_91957,RMVar_hsa_circ_191549,RMVar_hsa_circ_75955,RMVar_hsa_circ_191548,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546,RMVar_hsa_circ_269783,RMVar_hsa_circ_191553,RMVar_hsa_circ_329901 81067 RMVar_ID_81067 Human_SNP_ID_656429364 m1A Human chr19 - 4447438 4447436 4447438 CAGGCGGTGGGCTCCCTGGAGGAGCTAGCGAGAGTTGAGCCACAAGCAGTGAAGGGTTCGGCCAG CAGGCGGTGGGCTCCCTGGAGGAGCTAGCGAG__TTGAGCCACAAGCAGTGAAGGGTTCGGCCAG ACT A UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4447436..4447536 26863196 MeRIP-seq:(Medium) rs1293327025 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26769769 RMVar_hsa_circ_105129,RMVar_hsa_circ_114592,RMVar_hsa_circ_191547,RMVar_hsa_circ_80900,RMVar_hsa_circ_91957,RMVar_hsa_circ_191549,RMVar_hsa_circ_75955,RMVar_hsa_circ_191548,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546,RMVar_hsa_circ_269783,RMVar_hsa_circ_191553,RMVar_hsa_circ_329901 81068 RMVar_ID_81068 Human_SNP_ID_656429411 m1A Human chr19 + 4447553 4447553 4447553 GGGCCCCGGGGGCCAGAAGGCACGCCCACCTGAAACACCTTGTTCTGCAGCTTGATCTTCCGGTA GGGCCCCGGGGGCCAGAAGGCACGCCCACCTGCAACACCTTGTTCTGCAGCTTGATCTTCCGGTA A C AC011498.2 Ensembl:ENSG00000267030 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4447551..4447650 26863196 MeRIP-seq:(Medium) rs752067512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8489375 RMVar_hsa_circ_191552,RMVar_hsa_circ_98973 81069 RMVar_ID_81069 Human_SNP_ID_656429734 m1A Human chr19 + 4448396 4448396 4448396 TGAACGTGTAGATCTTCATGATGGAGGCGGCCACTGGGTCGGTGGAGAAGTGCTGGGAGGAGGGA TGAACGTGTAGATCTTCATGATGGAGGCGGCCGCTGGGTCGGTGGAGAAGTGCTGGGAGGAGGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4448257..4448450 26863196 MeRIP-seq:(Medium) rs778473018 Functional Loss SNV dbSNP153 33..33 33 - - - 81070 RMVar_ID_81070 Human_SNP_ID_656431040 m1A Human chr19 - 4452414 4452414 4452414 GCGTGTACTTCACCTGTCCGCTCACTGGGGCCACCCTGAGGAAGGACCAGCGGGACGCCTGCATC GCGTGTACTTCACCTGTCCGCTCACTGGGGCCGCCCTGAGGAAGGACCAGCGGGACGCCTGCATC T C UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4452351..4457722 32194978 MeRIP-seq:(Medium) rs751237087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381695,Human_RBP_ID_18191864 Human_Splice_Rec_1940090,Human_Splice_Rec_1940091,Human_Splice_Rec_1940116,Human_Splice_Rec_1940117,Human_Splice_Rec_1940141,Human_Splice_Rec_1940148,Human_Splice_Rec_1940149 RMVar_hsa_circ_21634,RMVar_hsa_circ_105129,RMVar_hsa_circ_114592,RMVar_hsa_circ_191547,RMVar_hsa_circ_80900,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546,RMVar_hsa_circ_191553,RMVar_hsa_circ_329901,RMVar_hsa_circ_191554,RMVar_hsa_circ_82772,RMVar_hsa_circ_23167,RMVar_hsa_circ_278838,RMVar_hsa_circ_191555 81071 RMVar_ID_81071 Human_SNP_ID_656431041 m1A Human chr19 - 4452414 4452414 4452414 GCGTGTACTTCACCTGTCCGCTCACTGGGGCCACCCTGAGGAAGGACCAGCGGGACGCCTGCATC GCGTGTACTTCACCTGTCCGCTCACTGGGGCCCCCCTGAGGAAGGACCAGCGGGACGCCTGCATC T G UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4452351..4457722 32194978 MeRIP-seq:(Medium) rs751237087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381695,Human_RBP_ID_18191864 Human_Splice_Rec_1940090,Human_Splice_Rec_1940091,Human_Splice_Rec_1940116,Human_Splice_Rec_1940117,Human_Splice_Rec_1940141,Human_Splice_Rec_1940148,Human_Splice_Rec_1940149 RMVar_hsa_circ_21634,RMVar_hsa_circ_105129,RMVar_hsa_circ_114592,RMVar_hsa_circ_191547,RMVar_hsa_circ_80900,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546,RMVar_hsa_circ_191553,RMVar_hsa_circ_329901,RMVar_hsa_circ_191554,RMVar_hsa_circ_82772,RMVar_hsa_circ_23167,RMVar_hsa_circ_278838,RMVar_hsa_circ_191555 81072 RMVar_ID_81072 Human_SNP_ID_656431639 m1A Human chr19 - 4454073 4454073 4454073 GTCTGTTCCCAGGGAAAAGGCCCACAAAGAGAAGCCCAACCAGCCAGCCCCCAGGCCGCCCCGCC GTCTGTTCCCAGGGAAAAGGCCCACAAAGAGAGGCCCAACCAGCCAGCCCCCAGGCCGCCCCGCC T C UBXN6 Ensembl:ENSG00000167671 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:4453926..4455232;chr19:4453903..4455727 26863196 MeRIP-seq:(Medium) rs934852467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913400,Human_RBP_ID_3954214,Human_RBP_ID_26816731 Human_Splice_Rec_1940086,Human_Splice_Rec_1940112,Human_Splice_Rec_1940144 Human_miRNA_ID_2333217,Human_miRNA_ID_2333218,Human_miRNA_ID_2966300,Human_miRNA_ID_2966301,Human_miRNA_ID_3118909,Human_miRNA_ID_3118910 RMVar_hsa_circ_105129,RMVar_hsa_circ_80900,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546,RMVar_hsa_circ_191553,RMVar_hsa_circ_329901,RMVar_hsa_circ_191554,RMVar_hsa_circ_82772,RMVar_hsa_circ_278838,RMVar_hsa_circ_191555,RMVar_hsa_circ_191556,RMVar_hsa_circ_373246 81073 RMVar_ID_81073 Human_SNP_ID_656432091 m1A Human chr19 - 4455559 4455559 4455559 CTTTAGGATTTTGCAGTGGGAGGGCGTTGTGCAGTGGAGTGATGCTGACGCTCCCTGGCTGAGGT CTTTAGGATTTTGCAGTGGGAGGGCGTTGTGCGGTGGAGTGATGCTGACGCTCCCTGGCTGAGGT T C UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4455557..4455717 26863196 MeRIP-seq:(Medium) rs1335357344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3580583,Human_RBP_ID_8100060,Human_RBP_ID_8199327 81074 RMVar_ID_81074 Human_SNP_ID_656432652 m1A Human chr19 - 4457485 4457485 4457485 AGGGGCTGGGAGCGGCACGCGAGGGTCAGGGGAGGGGGAGAGGCGCCGGGGGCGGACGAAGTCGG AGGGGCTGGGAGCGGCACGCGAGGGTCAGGGGGGGGGGAGAGGCGCCGGGGGCGGACGAAGTCGG T C UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4457483..4457775 26863196 MeRIP-seq:(Medium) rs1211014678 Functional Loss SNV dbSNP153 33..33 33 - - - 81075 RMVar_ID_81075 Human_SNP_ID_656432759 m1A Human chr19 + 4457743 4457720 4457744 CCGGCGGCGGGGGGCCGCGGGGGCGGGGGGGCACGGGGCCCAGTCGGGGACGGGGCCGCCGGAGA CCGGCGGCGG________________________GGGGCCCAGTCGGGGACGGGGCCGCCGGAGA GGGGGCCGCGGGGGCGGGGGGGCAC G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:4457601..4457800;chr19:4457601..4457777 26863196 MeRIP-seq:(Medium) rs765887592 Functional Loss DEL dbSNP153 11..34 33 - - - 81076 RMVar_ID_81076 Human_SNP_ID_656438263 m1A Human chr19 - 4472332 4472332 4472332 AAGGCGTGTGGCATGCTGACGGCGAGAGGCCCAGGCCGCGGAAAGCGGCTGCAGCGGCGGTAGCG AAGGCGTGTGGCATGCTGACGGCGAGAGGCCCGGGCCGCGGAAAGCGGCTGCAGCGGCGGTAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4472251..4474906 26863196 MeRIP-seq:(Medium) rs894533833 Functional Loss SNV dbSNP153 33..33 33 - - - 81077 RMVar_ID_81077 Human_SNP_ID_656438268 m1A Human chr19 - 4472338 4472338 4472338 GGCTTGAAGGCGTGTGGCATGCTGACGGCGAGAGGCCCAGGCCGCGGAAAGCGGCTGCAGCGGCG GGCTTGAAGGCGTGTGGCATGCTGACGGCGAGTGGCCCAGGCCGCGGAAAGCGGCTGCAGCGGCG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4472270..4472402 26863196 MeRIP-seq:(Medium) rs369828512 Functional Loss SNV dbSNP153 33..33 33 - - - 81078 RMVar_ID_81078 Human_SNP_ID_656438395 m1A Human chr19 + 4472469 4472467 4472469 GAGATGGGGCCGGTGGGGGGGGGGGGGGGGGCAGCGGGGGCCCCGGGCCGGAGGCGGGCACTGGA GAGATGGGGCCGGTGGGGGGGGGGGGGGGGG__GCGGGGGCCCCGGGCCGGAGGCGGGCACTGGA GCA G HDGFL2 Ensembl:ENSG00000167674 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4472262..4472482 26863196 MeRIP-seq:(Medium) rs1170771592 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_263754,Human_RBP_ID_908317,Human_RBP_ID_5371088,Human_RBP_ID_8198441,Human_RBP_ID_9426931,Human_RBP_ID_18461751,Human_RBP_ID_19091658,Human_RBP_ID_22358791 RMVar_hsa_circ_102558,RMVar_hsa_circ_191557 81079 RMVar_ID_81079 Human_SNP_ID_656438396 m1A Human chr19 + 4472469 4472469 4472469 GAGATGGGGCCGGTGGGGGGGGGGGGGGGGGCAGCGGGGGCCCCGGGCCGGAGGCGGGCACTGGA GAGATGGGGCCGGTGGGGGGGGGGGGGGGGGCGGCGGGGGCCCCGGGCCGGAGGCGGGCACTGGA A G HDGFL2 Ensembl:ENSG00000167674 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4472262..4472482 26863196 MeRIP-seq:(Medium) rs1329917773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263754,Human_RBP_ID_908317,Human_RBP_ID_5371088,Human_RBP_ID_8198441,Human_RBP_ID_9426931,Human_RBP_ID_18461751,Human_RBP_ID_19091658,Human_RBP_ID_22358791 RMVar_hsa_circ_102558,RMVar_hsa_circ_191557 81080 RMVar_ID_81080 Human_SNP_ID_656438951 m1A Human chr19 + 4474084 4474084 4474084 GTTCCAGGCCCTGAGAGGTACAGGCCAGCGGGAAGCAGGGACCCCAGGCTATTGTCATCCCCAGG GTTCCAGGCCCTGAGAGGTACAGGCCAGCGGGGAGCAGGGACCCCAGGCTATTGTCATCCCCAGG A G HDGFL2 Ensembl:ENSG00000167674 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4474081..4474569 26863196 MeRIP-seq:(Medium) rs1382789998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3587704 RMVar_hsa_circ_102558,RMVar_hsa_circ_191557 81081 RMVar_ID_81081 Human_SNP_ID_656439291 m1A Human chr19 + 4475244 4475244 4475244 GATTTCTCGGTGATTTCCTGGGTCAGTGGGTAAAGCCACCCCCTCACTGGCCTCTCACTGCAGAT GATTTCTCGGTGATTTCCTGGGTCAGTGGGTAGAGCCACCCCCTCACTGGCCTCTCACTGCAGAT A G HDGFL2 Ensembl:ENSG00000167674 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:4475231..4475416 26863410 MeRIP-seq:(Medium) rs1229102161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22546525 RMVar_hsa_circ_102558,RMVar_hsa_circ_191557 81082 RMVar_ID_81082 Human_SNP_ID_656443682 m1A Human chr19 + 4488796 4488796 4488796 TGGCCGTCACAGCGGTAACCGCCACAGCTGCCAGCGACAGGATGGAGAGCGACTCAGACTCAGAC TGGCCGTCACAGCGGTAACCGCCACAGCTGCCCGCGACAGGATGGAGAGCGACTCAGACTCAGAC A C HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4475255..4496940 32194978 MeRIP-seq:(Medium) rs765507022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4535524,Human_RBP_ID_6772466,Human_RBP_ID_9444083,Human_RBP_ID_26335234 Human_Splice_Rec_1940167,Human_Splice_Rec_1940197,Human_Splice_Rec_1940229,Human_Splice_Rec_1940237,Human_Splice_Rec_1940251 RMVar_hsa_circ_22131,RMVar_hsa_circ_19635,RMVar_hsa_circ_334157,RMVar_hsa_circ_308548,RMVar_hsa_circ_191559 81083 RMVar_ID_81083 Human_SNP_ID_656443697 m1A Human chr19 - 4488823 4488823 4488823 CTTCAGGCCACTGTTGTCGCTACTCTTGTCTGAGTCTGAGTCGCTCTCCATCCTGTCGCTGGCAG CTTCAGGCCACTGTTGTCGCTACTCTTGTCTGCGTCTGAGTCGCTCTCCATCCTGTCGCTGGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4488639..4488914 26863196 MeRIP-seq:(Medium) rs1316149305 Functional Loss SNV dbSNP153 33..33 33 - - - 81084 RMVar_ID_81084 Human_SNP_ID_656444675 m1A Human chr19 + 4491833 4491833 4491833 CACGGAGGGGCCCTCTGGGGGGACGGAAAAAAAAGGTAGCGTGCACTTGACTTTGTTTCCCATGC CACGGAGGGGCCCTCTGGGGGGACGGAAAAAAGAGGTAGCGTGCACTTGACTTTGTTTCCCATGC A G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4491522..4491877 26863196 MeRIP-seq:(Medium) rs1442934895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371089,Human_RBP_ID_18994097 Human_Splice_Rec_1940170,Human_Splice_Rec_1940171,Human_Splice_Rec_1940200,Human_Splice_Rec_1940201,Human_Splice_Rec_1940240,Human_Splice_Rec_1940241,Human_Splice_Rec_1940254,Human_Splice_Rec_1940255 RMVar_hsa_circ_22131,RMVar_hsa_circ_19635 81085 RMVar_ID_81085 Human_SNP_ID_656445705 m1A Human chr19 - 4493801 4493786 4493801 ACAGACACATCGGAGTCGGAGGAGGAGGAGGAAGAGGAGGAGGAGGACGCCGACCGCGCCATGGC ACAGACACATCGGAGTCGGAGGAGGAGGAGGA_______________CGCCGACCGCGCCATGGC GTCCTCCTCCTCCTCT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4493701..4493850 26863196 MeRIP-seq:(Medium) rs1568213975 Functional Loss DEL dbSNP153 33..47 33 - - - 81086 RMVar_ID_81086 Human_SNP_ID_656445717 m1A Human chr19 - 4493801 4493798 4493801 ACAGACACATCGGAGTCGGAGGAGGAGGAGGAAGAGGAGGAGGAGGACGCCGACCGCGCCATGGC ACAGACACATCGGAGTCGGAGGAGGAGGAGGA___GGAGGAGGAGGACGCCGACCGCGCCATGGC CTCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4493701..4493850 26863196 MeRIP-seq:(Medium) rs1568214024 Functional Loss DEL dbSNP153 33..35 33 - - - 81087 RMVar_ID_81087 Human_SNP_ID_656445719 m1A Human chr19 - 4493801 4493801 4493801 ACAGACACATCGGAGTCGGAGGAGGAGGAGGAAGAGGAGGAGGAGGACGCCGACCGCGCCATGGC ACAGACACATCGGAGTCGGAGGAGGAGGAGGAGGAGGAGGAGGAGGACGCCGACCGCGCCATGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4493701..4493850 26863196 MeRIP-seq:(Medium) rs533672657 Functional Loss SNV dbSNP153 33..33 33 - - - 81088 RMVar_ID_81088 Human_SNP_ID_656445750 m1A Human chr19 + 4493856 4493856 4493856 ATGTGTCTGTGAAGAAGCCTCCGAGGGGCAGGAAGCCAGGTAGGGCCCTCGTGCTCGCACATCTC ATGTGTCTGTGAAGAAGCCTCCGAGGGGCAGGGAGCCAGGTAGGGCCCTCGTGCTCGCACATCTC A G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4493689..4493877 26863196 MeRIP-seq:(Medium) rs775867906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912573,Human_RBP_ID_3956013,Human_RBP_ID_9380116,Human_RBP_ID_18996084 Human_Splice_Rec_1940173,Human_Splice_Rec_1940203,Human_Splice_Rec_1940257 RMVar_hsa_circ_19635 81089 RMVar_ID_81089 Human_SNP_ID_656445837 m1A Human chr19 + 4494054 4494054 4494054 GCCTGAACGGCCTCCGTCCAGCTCCAGCAGTGACAGGTGGGTGCTGGGGCTGGGGTCCCCTCTGG GCCTGAACGGCCTCCGTCCAGCTCCAGCAGTGGCAGGTGGGTGCTGGGGCTGGGGTCCCCTCTGG A G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4493964..4494080 26863196 MeRIP-seq:(Medium) rs1308188790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19091662 Human_Splice_Rec_1940174,Human_Splice_Rec_1940175,Human_Splice_Rec_1940204,Human_Splice_Rec_1940205,Human_Splice_Rec_1940258,Human_Splice_Rec_1940259 RMVar_hsa_circ_19635 81090 RMVar_ID_81090 Human_SNP_ID_656445981 m1A Human chr19 + 4494333 4494318 4494333 GGAGCGGAGGCGCGAGCGGGCCGACCGCGGGGAGGCTGAGCGGGGCAGCGGCGGCAGCAGCGGGG GGAGCGGAGGCGCGAGCG_______________GGCTGAGCGGGGCAGCGGCGGCAGCAGCGGGG GGGCCGACCGCGGGGA G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4494176..4494425 26863196 MeRIP-seq:(Medium) rs1250129444 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_240569,Human_RBP_ID_771987,Human_RBP_ID_912575,Human_RBP_ID_4535575,Human_RBP_ID_5375236,Human_RBP_ID_5650667,Human_RBP_ID_9328420,Human_RBP_ID_9380118,Human_RBP_ID_18996085,Human_RBP_ID_20433202,Human_RBP_ID_22533302,Human_RBP_ID_22718245,Human_RBP_ID_26335237,Human_RBP_ID_27814927 Human_miRNA_ID_2152215,Human_miRNA_ID_2420679 RMVar_hsa_circ_19635 81091 RMVar_ID_81091 Human_SNP_ID_656447973 m1A Human chr19 + 4499666 4499652 4499666 GAAGCTGGCCGGGGAGGAGCTGGCCGGGGAGGAGGCCCCCCAGGAGAAGGCGGAGGACAAGCCCA GAAGCTGGCCGGGGAGGAG______________GGCCCCCCAGGAGAAGGCGGAGGACAAGCCCA GCTGGCCGGGGAGGA G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4499525..4501361 26863196 MeRIP-seq:(Medium) rs895525730 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_240570,Human_RBP_ID_771989,Human_RBP_ID_912581,Human_RBP_ID_3954216,Human_RBP_ID_8233580,Human_RBP_ID_9380124,Human_RBP_ID_17656611,Human_RBP_ID_18192803,Human_RBP_ID_18412447,Human_RBP_ID_18996089,Human_RBP_ID_24545392,Human_RBP_ID_26335245,Human_RBP_ID_27815856 Human_Splice_Rec_1940187,Human_Splice_Rec_1940217,Human_Splice_Rec_1940271,Human_Splice_Rec_1940287,Human_Splice_Rec_1940289,Human_Splice_Rec_1940291 RMVar_hsa_circ_367625,RMVar_hsa_circ_328097 81092 RMVar_ID_81092 Human_SNP_ID_656447976 m1A Human chr19 + 4499663 4499653 4499664 GGAGAAGCTGGCCGGGGAGGAGCTGGCCGGGGAGGAGGCCCCCCAGGAGAAGGCGGAGGACAAGC GGAGAAGCTGGCCGGGGAGGAGC___________GAGGCCCCCCAGGAGAAGGCGGAGGACAAGC CTGGCCGGGGAG C HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4499584..4499759;chr19:4499465..4499751;chr19:4497939..4501361 26863196 MeRIP-seq:(Medium) rs758552443 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_240570,Human_RBP_ID_771989,Human_RBP_ID_912581,Human_RBP_ID_3954216,Human_RBP_ID_8233580,Human_RBP_ID_9380124,Human_RBP_ID_17656611,Human_RBP_ID_18192803,Human_RBP_ID_18412447,Human_RBP_ID_18996089,Human_RBP_ID_24545392,Human_RBP_ID_26335245,Human_RBP_ID_27815856 Human_Splice_Rec_1940187,Human_Splice_Rec_1940217,Human_Splice_Rec_1940271,Human_Splice_Rec_1940287,Human_Splice_Rec_1940289,Human_Splice_Rec_1940291 RMVar_hsa_circ_367625,RMVar_hsa_circ_328097 81093 RMVar_ID_81093 Human_SNP_ID_656447979 m1A Human chr19 + 4499666 4499654 4499667 GAAGCTGGCCGGGGAGGAGCTGGCCGGGGAGGAGGCCCCCCAGGAGAAGGCGGAGGACAAGCCCA GAAGCTGGCCGGGGAGGAGCT_____________GCCCCCCAGGAGAAGGCGGAGGACAAGCCCA TGGCCGGGGAGGAG T HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4499525..4501361 26863196 MeRIP-seq:(Medium) rs1312775517 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_240570,Human_RBP_ID_771989,Human_RBP_ID_912581,Human_RBP_ID_3954216,Human_RBP_ID_8233580,Human_RBP_ID_9380124,Human_RBP_ID_17656611,Human_RBP_ID_18192803,Human_RBP_ID_18412447,Human_RBP_ID_18996089,Human_RBP_ID_24545392,Human_RBP_ID_26335245,Human_RBP_ID_27815856 Human_Splice_Rec_1940187,Human_Splice_Rec_1940217,Human_Splice_Rec_1940271,Human_Splice_Rec_1940287,Human_Splice_Rec_1940289,Human_Splice_Rec_1940291 RMVar_hsa_circ_367625,RMVar_hsa_circ_328097 81094 RMVar_ID_81094 Human_SNP_ID_656447985 m1A Human chr19 + 4499663 4499663 4499663 GGAGAAGCTGGCCGGGGAGGAGCTGGCCGGGGAGGAGGCCCCCCAGGAGAAGGCGGAGGACAAGC GGAGAAGCTGGCCGGGGAGGAGCTGGCCGGGGGGGAGGCCCCCCAGGAGAAGGCGGAGGACAAGC A G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4499584..4499759;chr19:4499465..4499751;chr19:4497939..4501361 26863196 MeRIP-seq:(Medium) rs1012210187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240570,Human_RBP_ID_771989,Human_RBP_ID_912581,Human_RBP_ID_3954216,Human_RBP_ID_8233580,Human_RBP_ID_9380124,Human_RBP_ID_17656611,Human_RBP_ID_18192803,Human_RBP_ID_18412447,Human_RBP_ID_18996089,Human_RBP_ID_24545392,Human_RBP_ID_26335245,Human_RBP_ID_27815856 Human_Splice_Rec_1940187,Human_Splice_Rec_1940217,Human_Splice_Rec_1940271,Human_Splice_Rec_1940287,Human_Splice_Rec_1940289,Human_Splice_Rec_1940291 RMVar_hsa_circ_367625,RMVar_hsa_circ_328097 81095 RMVar_ID_81095 Human_SNP_ID_656448547 m1A Human chr19 + 4501243 4501243 4501243 GGCGAGGCCACATCACAGAAGGGGGAGAGCGCAGAGGACAAGGAGCACGAGGAGGGTCGGGACTC GGCGAGGCCACATCACAGAAGGGGGAGAGCGCGGAGGACAAGGAGCACGAGGAGGGTCGGGACTC A G HDGFL2 Ensembl:ENSG00000167674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4501149..4501361 26863196 MeRIP-seq:(Medium) rs768689461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380125,Human_RBP_ID_27468924,Human_RBP_ID_27815858 Human_Splice_Rec_1940188,Human_Splice_Rec_1940189,Human_Splice_Rec_1940218,Human_Splice_Rec_1940219,Human_Splice_Rec_1940272,Human_Splice_Rec_1940273,Human_Splice_Rec_1940288,Human_Splice_Rec_1940292,Human_Splice_Rec_1940293 Human_miRNA_ID_2255630,Human_miRNA_ID_2571343,Human_miRNA_ID_3045080 RMVar_hsa_circ_109204,RMVar_hsa_circ_191563 81096 RMVar_ID_81096 Human_SNP_ID_656448891 m1A Human chr19 - 4501994 4501994 4501994 CCTGGCTGCCCGCGGCTCAGCTCTCCTCGTCCAGGGCCTCCGAGTCCCCCCGTGCCCTCTCGCGC CCTGGCTGCCCGCGGCTCAGCTCTCCTCGTCCTGGGCCTCCGAGTCCCCCCGTGCCCTCTCGCGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4501865..4502111 26863196 MeRIP-seq:(Medium) rs1196819667 Functional Loss SNV dbSNP153 33..33 33 - - - 81097 RMVar_ID_81097 Human_SNP_ID_656448984 m1A Human chr19 - 4502118 4502113 4502119 TAGGCAGGAAAAAAAAACCCAAGGGAACAAATACAAACAGCACAGCGTTCCCCACAGTTCTCTGC TAGGCAGGAAAAAAAAACCCAAGGGAACAAA______CAGCACAGCGTTCCCCACAGTTCTCTGC GTTTGTA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4501560..4502175 32194978 MeRIP-seq:(Medium) rs1471811956 Functional Loss DEL dbSNP153 32..37 33 - - - 81098 RMVar_ID_81098 Human_SNP_ID_656451003 m1A Human chr19 + 4507258 4507258 4507258 TCTCAAGGTTTCTCACGGCCCGCCGGGGTGGGACTGCTGTCCACCAACATGTAAAACCTGTGACT TCTCAAGGTTTCTCACGGCCCGCCGGGGTGGGGCTGCTGTCCACCAACATGTAAAACCTGTGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4507235..4507401 26863196 MeRIP-seq:(Medium) rs532899028 Functional Loss SNV dbSNP153 33..33 33 - - - 81099 RMVar_ID_81099 Human_SNP_ID_656451004 m1A Human chr19 + 4507258 4507258 4507258 TCTCAAGGTTTCTCACGGCCCGCCGGGGTGGGACTGCTGTCCACCAACATGTAAAACCTGTGACT TCTCAAGGTTTCTCACGGCCCGCCGGGGTGGGTCTGCTGTCCACCAACATGTAAAACCTGTGACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4507235..4507401 26863196 MeRIP-seq:(Medium) rs532899028 Functional Loss SNV dbSNP153 33..33 33 - - - 81100 RMVar_ID_81100 Human_SNP_ID_656464882 m1A Human chr19 - 4542853 4542853 4542853 GGACAATGCCGGGGTTTCAGGCAGGAGACACGAGGAGGGCCTGCCCGGAAGTCACATCGGCAGCA GGACAATGCCGGGGTTTCAGGCAGGAGACACGGGGAGGGCCTGCCCGGAAGTCACATCGGCAGCA T C SEMA6B Ensembl:ENSG00000167680 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4542802..4543144 26863196 MeRIP-seq:(Medium) rs1373241905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523420,Human_RBP_ID_4536095,Human_RBP_ID_5115999,Human_RBP_ID_17935595 Human_miRNA_ID_2141508 RMVar_hsa_circ_91178,RMVar_hsa_circ_103555,RMVar_hsa_circ_127606,RMVar_hsa_circ_123993,RMVar_hsa_circ_94874,RMVar_hsa_circ_95180,RMVar_hsa_circ_127258,RMVar_hsa_circ_191566,RMVar_hsa_circ_191568,RMVar_hsa_circ_191569,RMVar_hsa_circ_191567,RMVar_hsa_circ_191565,RMVar_hsa_circ_95543,RMVar_hsa_circ_191573,RMVar_hsa_circ_78055,RMVar_hsa_circ_84199,RMVar_hsa_circ_191575,RMVar_hsa_circ_76960,RMVar_hsa_circ_191574,RMVar_hsa_circ_191571,RMVar_hsa_circ_191572,RMVar_hsa_circ_191570 81101 RMVar_ID_81101 Human_SNP_ID_656464990 m1A Human chr19 + 4543051 4543048 4543052 GACACACACCCTGCACGCGTGGCCCACTTGACACACACGCCCACAGCAGCCTTCGCTGGCACGCA GACACACACCCTGCACGCGTGGCCCACTTG____ACACGCCCACAGCAGCCTTCGCTGGCACGCA GACAC G HSALNG0123395 RNACentral:URS0000D5D14F lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4542642..4543683 32194978 MeRIP-seq:(Medium) rs924905192 Functional Loss DEL dbSNP153 31..34 33 - - - 81102 RMVar_ID_81102 Human_SNP_ID_656464991 m1A Human chr19 + 4543051 4543048 4543052 GACACACACCCTGCACGCGTGGCCCACTTGACACACACGCCCACAGCAGCCTTCGCTGGCACGCA GACACACACCCTGCACGCGTGGCCCACTTGAC__ACACGCCCACAGCAGCCTTCGCTGGCACGCA GACAC GAC HSALNG0123395 RNACentral:URS0000D5D14F lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4542642..4543683 32194978 MeRIP-seq:(Medium) rs924905192 Functional Loss DEL dbSNP153 33..34 33 - - - 81103 RMVar_ID_81103 Human_SNP_ID_656465344 m1A Human chr19 + 4543973 4543972 4543973 GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCCAGGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCC_GGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4543930..4544328 32194978 MeRIP-seq:(Medium) rs1408529429 Functional Loss DEL dbSNP153 33..33 33 - - - 81104 RMVar_ID_81104 Human_SNP_ID_656465345 m1A Human chr19 + 4543973 4543973 4543973 GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCCAGGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCCCGGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4543930..4544328 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81105 RMVar_ID_81105 Human_SNP_ID_656465346 m1A Human chr19 + 4543973 4543973 4543973 GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCCAGGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG GCATAGAGGCGGCCGTCGGGGGTCGGCTCCCCGGGCGCGGGGGGCTGCTCGGGGGCCCGGGCGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4543930..4544328 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81106 RMVar_ID_81106 Human_SNP_ID_656466815 m1A Human chr19 + 4548347 4548347 4548347 TCCCTGAGGTGCTGGCATTGGGCCGGACGAGGAACTTGAGGACCGTCCCCGCCTCAGAACCCAGG TCCCTGAGGTGCTGGCATTGGGCCGGACGAGGGACTTGAGGACCGTCCCCGCCTCAGAACCCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4546398..4550168 32194978 MeRIP-seq:(Medium) rs1265472059 Functional Loss SNV dbSNP153 33..33 33 - - - 81107 RMVar_ID_81107 Human_SNP_ID_656493945 m1A Human chr19 + 4642799 4642799 4642799 AGGGCAGGGTGCGCAGGATCTTATGGGCTGCCAGGAATACTTGGCTTTGACCCCAAGGGAGGTGG AGGGCAGGGTGCGCAGGATCTTATGGGCTGCCGGGAATACTTGGCTTTGACCCCAAGGGAGGTGG A G TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4642789..4643009 26863196 MeRIP-seq:(Medium) rs1011722042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8195871 81108 RMVar_ID_81108 Human_SNP_ID_656497285 m1A Human chr19 + 4654368 4654366 4654368 TGCACATTTTATTTATTTATTGTTTTGAGACAAAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAG TGCACATTTTATTTATTTATTGTTTTGAGAC__AGTCTCGCTGTGTCACCCAGGCTGGAGTGCAG CAA C TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1368106817 Functional Loss DEL dbSNP153 32..33 33 - - - 81109 RMVar_ID_81109 Human_SNP_ID_656499785 m1A Human chr19 - 4663210 4663207 4663210 GGAGGGTAGATTGGAGGCTGTGTAGAATGAGGACAGGACGGGTGGGGAGGGTAGATTGGAGGCTG GGAGGGTAGATTGGAGGCTGTGTAGAATGAGG___GGACGGGTGGGGAGGGTAGATTGGAGGCTG CTGT C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4663208..4663504 26863196 MeRIP-seq:(Medium) rs1391446266 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81110 RMVar_ID_81110 Human_SNP_ID_656499827 m1A Human chr19 - 4663295 4663250 4663295 GTAGATTGGAGGCTGTGTAGAATGAGGATGGGATGGGTGGAGAGGGCACAGATTGGAGGCTGTAG GTAGATTGGAGGCTGTGTAGAATGAGGATGGG_________________________________ CCCCATCCTCATTCTACAGCCTCCAATCTGTGCCCTCTCCACCCAT C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4663294..4663407 26863196 MeRIP-seq:(Medium) rs1568286852 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81111 RMVar_ID_81111 Human_SNP_ID_656499836 m1A Human chr19 - 4663258 4663258 4663258 TGGAGAGGGCACAGATTGGAGGCTGTAGAATGAGGATGGGGTGGGTGGGGAGGGTAGATTGGAGG TGGAGAGGGCACAGATTGGAGGCTGTAGAATGTGGATGGGGTGGGTGGGGAGGGTAGATTGGAGG T A MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4663255..4663506 26863196 MeRIP-seq:(Medium) rs1414864149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81112 RMVar_ID_81112 Human_SNP_ID_656499856 m1A Human chr19 - 4663295 4663295 4663295 GTAGATTGGAGGCTGTGTAGAATGAGGATGGGATGGGTGGAGAGGGCACAGATTGGAGGCTGTAG GTAGATTGGAGGCTGTGTAGAATGAGGATGGGGTGGGTGGAGAGGGCACAGATTGGAGGCTGTAG T C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4663294..4663407 26863196 MeRIP-seq:(Medium) rs1196305420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81113 RMVar_ID_81113 Human_SNP_ID_656501644 m1A Human chr19 + 4668613 4668611 4668613 TTTGAACAACTCACCTCATTGGTCCCTCCTTGAGAGGCGTAAGTGAACATACACGTATATTTGTC TTTGAACAACTCACCTCATTGGTCCCTCCTT__GAGGCGTAAGTGAACATACACGTATATTTGTC TGA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4659926..4670350 32194978 MeRIP-seq:(Medium) rs1358707774 Functional Loss DEL dbSNP153 32..33 33 - - - 81114 RMVar_ID_81114 Human_SNP_ID_656501645 m1A Human chr19 + 4668613 4668613 4668613 TTTGAACAACTCACCTCATTGGTCCCTCCTTGAGAGGCGTAAGTGAACATACACGTATATTTGTC TTTGAACAACTCACCTCATTGGTCCCTCCTTGGGAGGCGTAAGTGAACATACACGTATATTTGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4659926..4670350 32194978 MeRIP-seq:(Medium) rs1228985177 Functional Loss SNV dbSNP153 33..33 33 - - - 81115 RMVar_ID_81115 Human_SNP_ID_656502133 m1A Human chr19 + 4670188 4670188 4670188 CGTACCCCCGGGCCCACGTTATGGGAGAAGGAATGCACGACGCCGCCGGGCCGCACGTCAAACGC CGTACCCCCGGGCCCACGTTATGGGAGAAGGACTGCACGACGCCGCCGGGCCGCACGTCAAACGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:4670108..4670325 26863196 MeRIP-seq:(Medium) rs768257796 Functional Loss SNV dbSNP153 33..33 33 - - - 81116 RMVar_ID_81116 Human_SNP_ID_656502184 m1A Human chr19 + 4670264 4670264 4670264 GCTCGGACACCGCCTCCGCCGGCCTCAGCGCCACGGCCCCTAGGAGCAGCGCGGCCCACAAGCTC GCTCGGACACCGCCTCCGCCGGCCTCAGCGCCGCGGCCCCTAGGAGCAGCGCGGCCCACAAGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:4670151..4670325 26863410 MeRIP-seq:(Medium) rs769425351 Functional Loss SNV dbSNP153 33..33 33 - - - 81117 RMVar_ID_81117 Human_SNP_ID_656502203 m1A Human chr19 - 4670295 4670295 4670295 CGCCCAGCGGAGGGTGGAACGGCGTCGGCGCGAGCTTGTGGGCCGCGCTGCTCCTAGGGGCCGTG CGCCCAGCGGAGGGTGGAACGGCGTCGGCGCGTGCTTGTGGGCCGCGCTGCTCCTAGGGGCCGTG T A MYDGF Ensembl:ENSG00000074842 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4664876..4670375;chr19:4670102..4670350 26863196 MeRIP-seq:(Medium) rs370135731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4537854,Human_RBP_ID_5320047,Human_RBP_ID_8942389,Human_RBP_ID_17670151,Human_RBP_ID_18470408,Human_RBP_ID_22446326,Human_RBP_ID_23131504,Human_RBP_ID_23801676,Human_RBP_ID_26769960 Human_miRNA_ID_2757120 RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81118 RMVar_ID_81118 Human_SNP_ID_656502216 m1A Human chr19 - 4670309 4670309 4670309 GTCCAACATGGCGGCGCCCAGCGGAGGGTGGAACGGCGTCGGCGCGAGCTTGTGGGCCGCGCTGC GTCCAACATGGCGGCGCCCAGCGGAGGGTGGAGCGGCGTCGGCGCGAGCTTGTGGGCCGCGCTGC T C MYDGF Ensembl:ENSG00000074842 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:4670221..4670321 26863410 MeRIP-seq:(Medium) rs1053964827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770072,Human_RBP_ID_4557123,Human_RBP_ID_8490478,Human_RBP_ID_9088860,Human_RBP_ID_17670151,Human_RBP_ID_18470408,Human_RBP_ID_22448189,Human_RBP_ID_23131504,Human_RBP_ID_23801676 RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 81119 RMVar_ID_81119 Human_SNP_ID_656504635 m1A Human chr19 + 4675465 4675465 4675465 TGAGGTGGGGATGGTTCAGCTCCCAACCCCGGAACCCCTGGTGTGTACGGGTCAGGCAGACACAT TGAGGTGGGGATGGTTCAGCTCCCAACCCCGGCACCCCTGGTGTGTACGGGTCAGGCAGACACAT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4675323..4675722 32194978 MeRIP-seq:(Medium) rs1182417482 Functional Loss SNV dbSNP153 33..33 33 - - - 81120 RMVar_ID_81120 Human_SNP_ID_656504859 m1A Human chr19 + 4676201 4676201 4676201 GTGCTGGGGACGGTGGCTGGCCGGGCCAGGGGACTGAGAGGTCACAGGGAGCCCCAGGCGGAAGG GTGCTGGGGACGGTGGCTGGCCGGGCCAGGGGTCTGAGAGGTCACAGGGAGCCCCAGGCGGAAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4676151..4676320 32194978 MeRIP-seq:(Medium) rs936779398 Functional Loss SNV dbSNP153 33..33 33 - - - 81121 RMVar_ID_81121 Human_SNP_ID_656504912 m1A Human chr19 + 4676382 4676382 4676382 GCAACCAAGAAGCAGCGGACATAAAACCCAAGAGCGTTTAAAAAAGGATAAAAGGCGTCGGGGCG GCAACCAAGAAGCAGCGGACATAAAACCCAAGGGCGTTTAAAAAAGGATAAAAGGCGTCGGGGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4676259..4676504 26863196 MeRIP-seq:(Medium) rs577574909 Functional Loss SNV dbSNP153 33..33 33 - - - 81122 RMVar_ID_81122 Human_SNP_ID_656504929 m1A Human chr19 + 4676457 4676457 4676457 CGGCTCCTCGGGGCTGGCCAGCGCTGGGCGGGACAAAGTGCCTCACTGGGGCCCGCGGGCCACTC CGGCTCCTCGGGGCTGGCCAGCGCTGGGCGGGGCAAAGTGCCTCACTGGGGCCCGCGGGCCACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4676266..4676625;chr19:4676338..4676625 26863196 MeRIP-seq:(Medium) rs1314347216 Functional Loss SNV dbSNP153 33..33 33 - - - 81123 RMVar_ID_81123 Human_SNP_ID_656505251 m1A Human chr19 + 4677493 4677493 4677493 CCTCTCCAGGCTCCTGGTCCCCACTGTTGCCCATCACCCTGGGAATGCACCAAGCCACCCACTGG CCTCTCCAGGCTCCTGGTCCCCACTGTTGCCCGTCACCCTGGGAATGCACCAAGCCACCCACTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4677488..4677579 26863196 MeRIP-seq:(Medium) rs1228585782 Functional Loss SNV dbSNP153 33..33 33 - - - 81124 RMVar_ID_81124 Human_SNP_ID_656505639 m1A Human chr19 - 4679077 4679077 4679077 CGGTGAGGAGGGTGGGGCTTCTGCTGTAGAGGAGGGGGGGCCCTCAGTAAGCAGGGTGGAGCTTC CGGTGAGGAGGGTGGGGCTTCTGCTGTAGAGGGGGGGGGGCCCTCAGTAAGCAGGGTGGAGCTTC T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4679070..4679264 26863196 MeRIP-seq:(Medium) rs1368985507 Functional Loss SNV dbSNP153 33..33 33 - - - 81125 RMVar_ID_81125 Human_SNP_ID_656510627 m1A Human chr19 + 4695502 4695502 4695502 TCTCTGTGCTCGGGATGAACAGGGCCGGGGGGAGGAGGACGAGCTGGAGCCACTGCTGGGGCCGG TCTCTGTGCTCGGGATGAACAGGGCCGGGGGGGGGAGGACGAGCTGGAGCCACTGCTGGGGCCGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4695384..4695525 26863196 MeRIP-seq:(Medium) rs1189248355 Functional Loss SNV dbSNP153 33..33 33 - - - 81126 RMVar_ID_81126 Human_SNP_ID_656517280 m1A Human chr19 + 4719934 4719933 4719934 CGCATTAACCGCTCAGCTGACCTCAGGAGGGCAGGGGTGCCTGCGGGCAAGTGGGAGGAGAGATC CGCATTAACCGCTCAGCTGACCTCAGGAGGGC_GGGGTGCCTGCGGGCAAGTGGGAGGAGAGATC CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4719883..4722580 32194978 MeRIP-seq:(Medium) rs774511449 Functional Loss DEL dbSNP153 33..33 33 - - - 81127 RMVar_ID_81127 Human_SNP_ID_656518266 m1A Human chr19 - 4723616 4723616 4723616 CCGCCCCGGCCGCGACCCTGAACCCGCCATTGACCGGCCCCGCCTCGGCCCTGACCCTGCCCTCG CCGCCCCGGCCGCGACCCTGAACCCGCCATTGTCCGGCCCCGCCTCGGCCCTGACCCTGCCCTCG T A DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4723608..4723739 26863196 MeRIP-seq:(Medium) rs1445052325 Functional Loss SNV dbSNP153 33..33 33 - - - 81128 RMVar_ID_81128 Human_SNP_ID_656518619 m1A Human chr19 + 4724126 4724126 4724126 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCATGCGGTACCACTTTTGC TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGGTTCCCGGCCAACGCATGCGGTACCACTTTTGC A G tRNA-Gly-TCC-1-1 RNACentral:URS00000AED6F tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs867827159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1373831,Human_RBP_ID_1568703,Human_RBP_ID_5261622,Human_RBP_ID_5275330,Human_RBP_ID_5499828,Human_RBP_ID_5588267,Human_RBP_ID_6774954,Human_RBP_ID_8256235,Human_RBP_ID_8490684,Human_RBP_ID_17388311,Human_RBP_ID_18533115,Human_RBP_ID_18736317,Human_RBP_ID_20405801,Human_RBP_ID_22811394,Human_RBP_ID_23114834,Human_RBP_ID_23131526,Human_RBP_ID_24418827,Human_RBP_ID_24484580,Human_RBP_ID_24552974,Human_RBP_ID_26654550,Human_RBP_ID_26749567 81129 RMVar_ID_81129 Human_SNP_ID_656518620 m1A Human chr19 + 4724126 4724126 4724126 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCATGCGGTACCACTTTTGC TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGTTTCCCGGCCAACGCATGCGGTACCACTTTTGC A T tRNA-Gly-TCC-1-1 RNACentral:URS00000AED6F tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs867827159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1373831,Human_RBP_ID_1568703,Human_RBP_ID_5261622,Human_RBP_ID_5275330,Human_RBP_ID_5499828,Human_RBP_ID_5588267,Human_RBP_ID_6774954,Human_RBP_ID_8256235,Human_RBP_ID_8490684,Human_RBP_ID_17388311,Human_RBP_ID_18533115,Human_RBP_ID_18736317,Human_RBP_ID_20405801,Human_RBP_ID_22811394,Human_RBP_ID_23114834,Human_RBP_ID_23131526,Human_RBP_ID_24418827,Human_RBP_ID_24484580,Human_RBP_ID_24552974,Human_RBP_ID_26654550,Human_RBP_ID_26749567 81130 RMVar_ID_81130 Human_SNP_ID_656518960 m1A Human chr19 - 4724605 4724605 4724605 ACAGGTCAGCTGTTTTTCCTAACCGGAGAGTAATACTATTTGAAATTCACCGAAAGAACGATTCT ACAGGTCAGCTGTTTTTCCTAACCGGAGAGTAGTACTATTTGAAATTCACCGAAAGAACGATTCT T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4724556..4724662 26863196 MeRIP-seq:(Medium) rs1428755542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23131529 81131 RMVar_ID_81131 Human_SNP_ID_656519026 m1A Human chr19 - 4724650 4724650 4724650 ATTCGCCTCACACGCGAAAGGTCCCCGGTTCGATCCCGGGCGGAAACAGGTCAGCTGTTTTTCCT ATTCGCCTCACACGCGAAAGGTCCCCGGTTCGGTCCCGGGCGGAAACAGGTCAGCTGTTTTTCCT T C DPP9 Ensembl:ENSG00000142002 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs532363429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55660,Human_RBP_ID_241669,Human_RBP_ID_279797,Human_RBP_ID_524206,Human_RBP_ID_1017226,Human_RBP_ID_1190797,Human_RBP_ID_1240089,Human_RBP_ID_1295119,Human_RBP_ID_1373836,Human_RBP_ID_1568710,Human_RBP_ID_1890326,Human_RBP_ID_3574170,Human_RBP_ID_4570832,Human_RBP_ID_5261623,Human_RBP_ID_5275365,Human_RBP_ID_5421676,Human_RBP_ID_5443263,Human_RBP_ID_5468957,Human_RBP_ID_5499829,Human_RBP_ID_5651329,Human_RBP_ID_6774989,Human_RBP_ID_8256236,Human_RBP_ID_8490692,Human_RBP_ID_8835669,Human_RBP_ID_9258784,Human_RBP_ID_9292507,Human_RBP_ID_13480394,Human_RBP_ID_17010679,Human_RBP_ID_17583020,Human_RBP_ID_17696079,Human_RBP_ID_17928286,Human_RBP_ID_18208442,Human_RBP_ID_18306366,Human_RBP_ID_18441684,Human_RBP_ID_18514977,Human_RBP_ID_18532567,Human_RBP_ID_18545485,Human_RBP_ID_18736325,Human_RBP_ID_20405835,Human_RBP_ID_22391296,Human_RBP_ID_22531597,Human_RBP_ID_22811399,Human_RBP_ID_23131529,Human_RBP_ID_23179337,Human_RBP_ID_23802223,Human_RBP_ID_24418829,Human_RBP_ID_24532652,Human_RBP_ID_24552978,Human_RBP_ID_26469196,Human_RBP_ID_26786149,Human_RBP_ID_26992325,Human_RBP_ID_27157700,Human_RBP_ID_27276123,Human_RBP_ID_27469482,Human_RBP_ID_27562656,Human_RBP_ID_27681798 Human_Splice_Rec_1940769 81132 RMVar_ID_81132 Human_SNP_ID_656539340 m1A Human chr19 - 4791814 4791814 4791814 CCTCCGCCAGGCCATGGGCCGGCCGCCGGGGGACGGGGAGACGGAGGATCAGAGCCCGGACGGGC CCTCCGCCAGGCCATGGGCCGGCCGCCGGGGGGCGGGGAGACGGAGGATCAGAGCCCGGACGGGC T C AC005523.2 Ensembl:ENSG00000269604 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4791774..4792013;chr19:4791780..4792025 26863196 MeRIP-seq:(Medium) rs1347846336 Functional Loss SNV dbSNP153 33..33 33 - - - 81133 RMVar_ID_81133 Human_SNP_ID_656540348 m1A Human chr19 - 4794474 4794474 4794474 GCTTGCAACCTGCCCACTTATTAAATAAACAGAACACCAAACCAACCGAAAGCTATGCAAGTGGC GCTTGCAACCTGCCCACTTATTAAATAAACAGCACACCAAACCAACCGAAAGCTATGCAAGTGGC T G AC005523.2 Ensembl:ENSG00000269604 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:4794128..4794778 32194978 MeRIP-seq:(Medium) rs1375714205 Functional Loss SNV dbSNP153 33..33 33 - - - 81134 RMVar_ID_81134 Human_SNP_ID_656547386 m1A Human chr19 - 4817354 4817354 4817354 AGACGCCACTCCAACTTTCTGTAGAAGATACCACCTCTCCAAATACCAAGCCGTGCCCACCTACT AGACGCCACTCCAACTTTCTGTAGAAGATACCCCCTCTCCAAATACCAAGCCGTGCCCACCTACT T G TICAM1 Ensembl:ENSG00000127666 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4817304..4817387 26863196 MeRIP-seq:(Medium) rs773920190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27276576,Human_RBP_ID_27469894 81135 RMVar_ID_81135 Human_SNP_ID_656551464 m1A Human chr19 - 4831658 4831658 4831658 CCGCGGGCAACTCCGCAGAAGCCCCAGCCCCCAGGACCCCAGGACCCAGTGGCGCAGCCGGCAGC CCGCGGGCAACTCCGCAGAAGCCCCAGCCCCCGGGACCCCAGGACCCAGTGGCGCAGCCGGCAGC T C TICAM1 Ensembl:ENSG00000127666 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4831566..4831659 26863196 MeRIP-seq:(Medium) rs11466709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557940 Human_Splice_Rec_1941223 81136 RMVar_ID_81136 Human_SNP_ID_656553716 m1A Human chr19 - 4839254 4839254 4839254 TGGTGGAATATGTGGCCCAGAACACACCTGTCACGTGGCTCGTGGGACCCTTTGCCCCTGGAATC TGGTGGAATATGTGGCCCAGAACACACCTGTCGCGTGGCTCGTGGGACCCTTTGCCCCTGGAATC T C PLIN3 Ensembl:ENSG00000105355 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4839205..4839322 26863196 MeRIP-seq:(Medium) rs566761137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9328425,Human_RBP_ID_17655828,Human_RBP_ID_18192805,Human_RBP_ID_22446327 Human_miRNA_ID_2878117 RMVar_hsa_circ_92029,RMVar_hsa_circ_92973,RMVar_hsa_circ_100935,RMVar_hsa_circ_191600,RMVar_hsa_circ_191602,RMVar_hsa_circ_84442,RMVar_hsa_circ_191601,RMVar_hsa_circ_191599 81137 RMVar_ID_81137 Human_SNP_ID_656555593 m1A Human chr19 + 4844727 4844727 4844727 GCCCTGGAGCTGCTTCTGGTTCCAGCTGAGCCACATCTGGTGCAGCTTCTCCTGGCCTTCCACCA GCCCTGGAGCTGCTTCTGGTTCCAGCTGAGCCGCATCTGGTGCAGCTTCTCCTGGCCTTCCACCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4844676..4844750 32194978 MeRIP-seq:(Medium) rs1319908719 Functional Loss SNV dbSNP153 33..33 33 - - - 81138 RMVar_ID_81138 Human_SNP_ID_656557928 m1A Human chr19 + 4852151 4852151 4852151 CATGACCGATTGGACGCCGCCGGTCACTACGGACTTTGTCTTGTCCACGCCGCTCTGCACAGCAC CATGACCGATTGGACGCCGCCGGTCACTACGGTCTTTGTCTTGTCCACGCCGCTCTGCACAGCAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4852101..4852175 32194978 MeRIP-seq:(Medium) rs1175152547 Functional Loss SNV dbSNP153 33..33 33 - - - 81139 RMVar_ID_81139 Human_SNP_ID_656560419 m1A Human chr19 + 4859915 4859911 4859915 GGGTCCTCACTCCCTTCTCTGCTGCGTCGCAGACAGTCTTGATGTGCGGGTAGCTCTCCTTGGTG GGGTCCTCACTCCCTTCTCTGCTGCGTCG____CAGTCTTGATGTGCGGGTAGCTCTCCTTGGTG GCAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4859865..4860069 26863196 MeRIP-seq:(Medium) rs767335755 Functional Loss DEL dbSNP153 30..33 33 - - - 81140 RMVar_ID_81140 Human_SNP_ID_656560430 m1A Human chr19 - 4859937 4859937 4859937 TGGTGTCCGCAGCCTATGCCTCCACCAAGGAGAGCTACCCGCACATCAAGACTGTCTGCGACGCA TGGTGTCCGCAGCCTATGCCTCCACCAAGGAGTGCTACCCGCACATCAAGACTGTCTGCGACGCA T A PLIN3 Ensembl:ENSG00000105355 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:4859826..4859975 32194978 MeRIP-seq:(Medium) rs1568380409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1941228,Human_Splice_Rec_1941242,Human_Splice_Rec_1941264,Human_Splice_Rec_1941276,Human_Splice_Rec_1941284,Human_Splice_Rec_1941292 Human_miRNA_ID_2077260 RMVar_hsa_circ_92029,RMVar_hsa_circ_81635,RMVar_hsa_circ_191599,RMVar_hsa_circ_191603,RMVar_hsa_circ_375216,RMVar_hsa_circ_323458,RMVar_hsa_circ_191605,RMVar_hsa_circ_326931,RMVar_hsa_circ_191606 81141 RMVar_ID_81141 Human_SNP_ID_656560867 m1A Human chr19 + 4861281 4861281 4861281 CCAGGGCACCCTGGGGTGGGAAGCCTCCTTGCACGGGAATCACAGGGTCGGGGCAGTCCCTGGTC CCAGGGCACCCTGGGGTGGGAAGCCTCCTTGCCCGGGAATCACAGGGTCGGGGCAGTCCCTGGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4861280..4861350 26863196 MeRIP-seq:(Medium) rs1398693427 Functional Loss SNV dbSNP153 33..33 33 - - - 81142 RMVar_ID_81142 Human_SNP_ID_656560940 m1A Human chr19 - 4861413 4861413 4861413 GGCAGGCTGTACCTGACTGTTCCTCTCTCCTCAGCGTCTGCTGCAGAGACCATGTCTGCCGACGG GGCAGGCTGTACCTGACTGTTCCTCTCTCCTCCGCGTCTGCTGCAGAGACCATGTCTGCCGACGG T G PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4861376..4861425 26863196 MeRIP-seq:(Medium) rs1339777526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557942,Human_RBP_ID_18996107,Human_RBP_ID_19091702,Human_RBP_ID_22661784,Human_RBP_ID_22741615 Human_Splice_Rec_1941227,Human_Splice_Rec_1941241,Human_Splice_Rec_1941263,Human_Splice_Rec_1941283,Human_Splice_Rec_1941291 81143 RMVar_ID_81143 Human_SNP_ID_656562814 m1A Human chr19 + 4867531 4867531 4867531 AGCAAATCCCACCCCGAGAAAGGCCCTCCCCGACCCCTCCGGCCCCTGGGGTGCCCCAGGACTCC AGCAAATCCCACCCCGAGAAAGGCCCTCCCCGCCCCCTCCGGCCCCTGGGGTGCCCCAGGACTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4867530..4867626 26863196 MeRIP-seq:(Medium) rs1380798857 Functional Loss SNV dbSNP153 33..33 33 - - - 81144 RMVar_ID_81144 Human_SNP_ID_656562816 m1A Human chr19 - 4867536 4867536 4867536 TCCATGGAGTCCTGGGGCACCCCAGGGGCCGGAGGGGTCGGGGAGGGCCTTTCTCGGGGTGGGAT TCCATGGAGTCCTGGGGCACCCCAGGGGCCGGTGGGGTCGGGGAGGGCCTTTCTCGGGGTGGGAT T A PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4867533..4867632;chr19:4867535..4867621 26863196 MeRIP-seq:(Medium) rs1267002899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371095,Human_RBP_ID_19094644 81145 RMVar_ID_81145 Human_SNP_ID_656562817 m1A Human chr19 - 4867536 4867536 4867536 TCCATGGAGTCCTGGGGCACCCCAGGGGCCGGAGGGGTCGGGGAGGGCCTTTCTCGGGGTGGGAT TCCATGGAGTCCTGGGGCACCCCAGGGGCCGGGGGGGTCGGGGAGGGCCTTTCTCGGGGTGGGAT T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4867533..4867632;chr19:4867535..4867621 26863196 MeRIP-seq:(Medium) rs1267002899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371095,Human_RBP_ID_19094644 81146 RMVar_ID_81146 Human_SNP_ID_656576341 m1A Human chr19 - 4909551 4909551 4909551 CGTGGCCCGGACCCCGCGCGGACTTGCGTGCGACCCGGAGCGCCCGCTCGGCAAACGCTGCCCGC CGTGGCCCGGACCCCGCGCGGACTTGCGTGCGTCCCGGAGCGCCCGCTCGGCAAACGCTGCCCGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:4909501..4910473;chr19:4909501..4910423 26863196 MeRIP-seq:(Medium) rs1270307979 Functional Loss SNV dbSNP153 33..33 33 - - - 81147 RMVar_ID_81147 Human_SNP_ID_656576349 m1A Human chr19 + 4909559 4909559 4909559 CGTTTGCCGAGCGGGCGCTCCGGGTCGCACGCAAGTCCGCGCGGGGTCCGGGCCACGCACGCGGT CGTTTGCCGAGCGGGCGCTCCGGGTCGCACGCGAGTCCGCGCGGGGTCCGGGCCACGCACGCGGT A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4909462..4910423 26863196 MeRIP-seq:(Medium) rs1221554797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242034,Human_RBP_ID_4540878,Human_RBP_ID_5469548,Human_RBP_ID_18420836,Human_RBP_ID_24374781 Human_Splice_Rec_1941331,Human_Splice_Rec_1941363,Human_Splice_Rec_1941385,Human_Splice_Rec_1941417 81148 RMVar_ID_81148 Human_SNP_ID_656582938 m1A Human chr19 - 4930736 4930736 4930736 GCCTCAAACCACGCCCCCATGTTCGTGTCCCGAGCATCGACGTACTCATTGACCTGTGAGGAATG GCCTCAAACCACGCCCCCATGTTCGTGTCCCGCGCATCGACGTACTCATTGACCTGTGAGGAATG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4910817..4932975 26863196 MeRIP-seq:(Medium) rs1442594870 Functional Loss SNV dbSNP153 33..33 33 - - - 81149 RMVar_ID_81149 Human_SNP_ID_656586711 m1A Human chr19 - 4941728 4941728 4941728 GACGGCCCGCTCTTCCCTGGGCACGGGGCGGCAGGGTCAGCTCCGGCGGGGCCCGGCCAAGCCAG GACGGCCCGCTCTTCCCTGGGCACGGGGCGGCCGGGTCAGCTCCGGCGGGGCCCGGCCAAGCCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4941726..4941800 26863196 MeRIP-seq:(Medium) rs1362560752 Functional Loss SNV dbSNP153 33..33 33 - - - 81150 RMVar_ID_81150 Human_SNP_ID_656590921 m1A Human chr19 + 4954480 4954480 4954480 CCCCAGGACGGGCAAGGGCAAGTGGAAGCGGAAGTCGGCAGGTGAGAATCTCGTGGGTGTGGGGT CCCCAGGACGGGCAAGGGCAAGTGGAAGCGGAGGTCGGCAGGTGAGAATCTCGTGGGTGTGGGGT A G UHRF1 Ensembl:ENSG00000276043 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:4954426..4954683 26863410 MeRIP-seq:(Medium) rs746655283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910293 Human_Splice_Rec_1941325,Human_Splice_Rec_1941357,Human_Splice_Rec_1941379,Human_Splice_Rec_1941411,Human_Splice_Rec_1941443,Human_Splice_Rec_1941475,Human_Splice_Rec_1941505,Human_Splice_Rec_1941537 RMVar_hsa_circ_335636 81151 RMVar_ID_81151 Human_SNP_ID_656592744 m1A Human chr19 - 4960385 4960384 4960386 CCCCCGGCTCTCATCACTCACAGCTCAGCTCAAGTCACCTCCCTTATGGGGCCTTCCCTGACACC CCCCCGGCTCTCATCACTCACAGCTCAGCTC__GTCACCTCCCTTATGGGGCCTTCCCTGACACC CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4960204..4960590 26863196 MeRIP-seq:(Medium) rs1446261460 Functional Loss DEL dbSNP153 32..33 33 - - - 81152 RMVar_ID_81152 Human_SNP_ID_656595542 m1A Human chr19 - 4969198 4969198 4969198 CTGAGGCGGCGTGCGCGGCCCGGTCCGGGAGCAGCGGCGCGCTCTCCCCCGCCCTCGGCGTCGCA CTGAGGCGGCGTGCGCGGCCCGGTCCGGGAGCCGCGGCGCGCTCTCCCCCGCCCTCGGCGTCGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4969161..4969235 26863196 MeRIP-seq:(Medium) rs1254988992 Functional Loss SNV dbSNP153 33..33 33 - - - 81153 RMVar_ID_81153 Human_SNP_ID_656610000 m1A Human chr19 - 5019341 5019341 5019341 GTCCACACCAACACCTGCACACCAACACCCACACCAACACCTGCACGCCAACGTCCACACCAACA GTCCACACCAACACCTGCACACCAACACCCACGCCAACACCTGCACGCCAACGTCCACACCAACA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:5019315..5019444 26863196 MeRIP-seq:(Medium) rs1432557120 Functional Loss SNV dbSNP153 33..33 33 - - - 81154 RMVar_ID_81154 Human_SNP_ID_656621195 m1A Human chr19 - 5055557 5055545 5055557 GCCTGCTGCGGGGTGCCCACCCGGCCCCCATCACGGCCACCATCTCTGCTCACCAAGAAGCCAGT GCCTGCTGCGGGGTGCCCACCCGGCCCCCATC____________TCTGCTCACCAAGAAGCCAGT AGATGGTGGCCGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5055552..5055661 26863196 MeRIP-seq:(Medium) rs1463479715 Functional Loss DEL dbSNP153 33..44 33 - - - 81155 RMVar_ID_81155 Human_SNP_ID_656633447 m1A Human chr19 - 5094390 5094390 5094390 TGATGAAATCTAACTTCAAAGGCCCTTACTGCAGCCCCCGACCTCTGACGTTTGGCCTCTGCCAG TGATGAAATCTAACTTCAAAGGCCCTTACTGCGGCCCCCGACCTCTGACGTTTGGCCTCTGCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5094341..5094503 26863196 MeRIP-seq:(Medium) rs956636198 Functional Loss SNV dbSNP153 33..33 33 - - - 81156 RMVar_ID_81156 Human_SNP_ID_656644273 m1A Human chr19 + 5131129 5131129 5131129 GGCCAACCAAGGCCAAGAGCGAGCGGAAGAAGAAGAGCTTCGGCCTGCTGCCCCCACAGCTGCCG GGCCAACCAAGGCCAAGAGCGAGCGGAAGAAGGAGAGCTTCGGCCTGCTGCCCCCACAGCTGCCG A G KDM4B Ensembl:ENSG00000127663 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5131050..5131299 26863196 MeRIP-seq:(Medium) rs1263192999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910321,Human_RBP_ID_8839648,Human_RBP_ID_18738248,Human_RBP_ID_18996130 Human_Splice_Rec_1941566,Human_Splice_Rec_1941610,Human_Splice_Rec_1941680,Human_Splice_Rec_1941720,Human_Splice_Rec_1941754 Human_miRNA_ID_2223746,Human_miRNA_ID_2486816,Human_miRNA_ID_3075181 RMVar_hsa_circ_24338,RMVar_hsa_circ_126656,RMVar_hsa_circ_191620,RMVar_hsa_circ_99491,RMVar_hsa_circ_81306,RMVar_hsa_circ_191626,RMVar_hsa_circ_191627,RMVar_hsa_circ_123207,RMVar_hsa_circ_78325,RMVar_hsa_circ_191631,RMVar_hsa_circ_116647,RMVar_hsa_circ_376208,RMVar_hsa_circ_350586,RMVar_hsa_circ_117265,RMVar_hsa_circ_93647,RMVar_hsa_circ_191640,RMVar_hsa_circ_191642,RMVar_hsa_circ_191643,RMVar_hsa_circ_191641,RMVar_hsa_circ_191639,RMVar_hsa_circ_121383,RMVar_hsa_circ_191654,RMVar_hsa_circ_102682,RMVar_hsa_circ_125046,RMVar_hsa_circ_191651,RMVar_hsa_circ_191652,RMVar_hsa_circ_68757,RMVar_hsa_circ_191658,RMVar_hsa_circ_191653,RMVar_hsa_circ_269053,RMVar_hsa_circ_342611,RMVar_hsa_circ_274190,RMVar_hsa_circ_318523,RMVar_hsa_circ_265033,RMVar_hsa_circ_191659,RMVar_hsa_circ_191660 81157 RMVar_ID_81157 Human_SNP_ID_656644275 m1A Human chr19 - 5131135 5131135 5131135 CGGGGGCGGCAGCTGTGGGGGCAGCAGGCCGAAGCTCTTCTTCTTCCGCTCGCTCTTGGCCTTGG CGGGGGCGGCAGCTGTGGGGGCAGCAGGCCGAGGCTCTTCTTCTTCCGCTCGCTCTTGGCCTTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:5131031..5131268;chr19:5131034..5131296 26863196 MeRIP-seq:(Medium) rs776441464 Functional Loss SNV dbSNP153 33..33 33 - - - 81158 RMVar_ID_81158 Human_SNP_ID_656644348 m1A Human chr19 - 5131283 5131281 5131284 CTAGCTCCTCACTGGGCACCTCAGGGGGCACGACATTAAGGGGTGCCGGCAGGGGGCTCTCCTCC CTAGCTCCTCACTGGGCACCTCAGGGGGCAC___ATTAAGGGGTGCCGGCAGGGGGCTCTCCTCC TGTC T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5113326..5135450 32194978 MeRIP-seq:(Medium) rs1421043538 Functional Loss DEL dbSNP153 32..34 33 - - - 81159 RMVar_ID_81159 Human_SNP_ID_656651593 m1A Human chr19 - 5152198 5152198 5152198 AGGCACAGAGTGGGCACAGGCACTGGCACCAGACCATCAAAGCCCAGGAGCCGGGGTGAGGCGAG AGGCACAGAGTGGGCACAGGCACTGGCACCAGTCCATCAAAGCCCAGGAGCCGGGGTGAGGCGAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5152147..5152847 32194978 MeRIP-seq:(Medium) rs894197988 Functional Loss SNV dbSNP153 33..33 33 - - - 81160 RMVar_ID_81160 Human_SNP_ID_656651913 m1A Human chr19 - 5153187 5153187 5153187 ACCCCCCAACCTCCCCGACCCCGGCCCTCTCCAGGGCAACCGCCCCCCTCCCCCACCAAGGAAAT ACCCCCCAACCTCCCCGACCCCGGCCCTCTCCCGGGCAACCGCCCCCCTCCCCCACCAAGGAAAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5153138..5153215 26863196 MeRIP-seq:(Medium) rs1235447819 Functional Loss SNV dbSNP153 33..33 33 - - - 81161 RMVar_ID_81161 Human_SNP_ID_656666724 m1A Human chr19 - 5205851 5205851 5205851 TGCGGTTGAGGGGGACGCTGCTGTAAGAGGAGAGAGATGACAGTGGTCCTCCTCTGAGAGCCTGA TGCGGTTGAGGGGGACGCTGCTGTAAGAGGAGGGAGATGACAGTGGTCCTCCTCTGAGAGCCTGA T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1455186700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526029,Human_RBP_ID_5116008,Human_RBP_ID_17696283,Human_RBP_ID_17935180,Human_RBP_ID_24484770 RMVar_hsa_circ_81272,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_98100,RMVar_hsa_circ_191663,RMVar_hsa_circ_127540,RMVar_hsa_circ_191664,RMVar_hsa_circ_109409,RMVar_hsa_circ_97702,RMVar_hsa_circ_105376,RMVar_hsa_circ_88341,RMVar_hsa_circ_191668,RMVar_hsa_circ_191670,RMVar_hsa_circ_191672,RMVar_hsa_circ_84269,RMVar_hsa_circ_191673,RMVar_hsa_circ_191671,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665 81162 RMVar_ID_81162 Human_SNP_ID_656666725 m1A Human chr19 - 5205851 5205851 5205851 TGCGGTTGAGGGGGACGCTGCTGTAAGAGGAGAGAGATGACAGTGGTCCTCCTCTGAGAGCCTGA TGCGGTTGAGGGGGACGCTGCTGTAAGAGGAGCGAGATGACAGTGGTCCTCCTCTGAGAGCCTGA T G PTPRS Ensembl:ENSG00000105426 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1455186700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526029,Human_RBP_ID_5116008,Human_RBP_ID_17696283,Human_RBP_ID_17935180,Human_RBP_ID_24484770 RMVar_hsa_circ_81272,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_98100,RMVar_hsa_circ_191663,RMVar_hsa_circ_127540,RMVar_hsa_circ_191664,RMVar_hsa_circ_109409,RMVar_hsa_circ_97702,RMVar_hsa_circ_105376,RMVar_hsa_circ_88341,RMVar_hsa_circ_191668,RMVar_hsa_circ_191670,RMVar_hsa_circ_191672,RMVar_hsa_circ_84269,RMVar_hsa_circ_191673,RMVar_hsa_circ_191671,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665 81163 RMVar_ID_81163 Human_SNP_ID_656667130 m1A Human chr19 - 5206808 5206808 5206808 TGAGTACCAGTTCTGTTACCAGGCGGCACTGGAGTACCTCGGAAGCTTTGACCACTATGCAACCT TGAGTACCAGTTCTGTTACCAGGCGGCACTGGGGTACCTCGGAAGCTTTGACCACTATGCAACCT T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5206576..5206825 32194978 MeRIP-seq:(Medium) rs1265207217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526052,Human_RBP_ID_910330,Human_RBP_ID_6780397,Human_RBP_ID_8836623,Human_RBP_ID_9292638,Human_RBP_ID_13501781,Human_RBP_ID_17935601,Human_RBP_ID_18738291 Human_Splice_Rec_1941912,Human_Splice_Rec_1941966,Human_Splice_Rec_1942028,Human_Splice_Rec_1942078 RMVar_hsa_circ_81272,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_98100,RMVar_hsa_circ_191663,RMVar_hsa_circ_127540,RMVar_hsa_circ_191664,RMVar_hsa_circ_109409,RMVar_hsa_circ_97702,RMVar_hsa_circ_105376,RMVar_hsa_circ_88341,RMVar_hsa_circ_191668,RMVar_hsa_circ_191670,RMVar_hsa_circ_191672,RMVar_hsa_circ_84269,RMVar_hsa_circ_191673,RMVar_hsa_circ_191671,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665 81164 RMVar_ID_81164 Human_SNP_ID_656669768 m1A Human chr19 - 5214574 5214574 5214574 GTCGGCGACCATCGTCATGATGACGCGGCTGGAGGAGAAGTCACGGGTGAGCCTTGGACCCCACG GTCGGCGACCATCGTCATGATGACGCGGCTGGGGGAGAAGTCACGGGTGAGCCTTGGACCCCACG T C PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5214572..5214669 26863196 MeRIP-seq:(Medium) rs867284088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907162,Human_RBP_ID_3954239,Human_RBP_ID_8836643,Human_RBP_ID_18470415,Human_RBP_ID_18996153,Human_RBP_ID_26335281 Human_Splice_Rec_1941821,Human_Splice_Rec_1941895,Human_Splice_Rec_1941949,Human_Splice_Rec_1942011,Human_Splice_Rec_1942061 RMVar_hsa_circ_2647,RMVar_hsa_circ_81272,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_98100,RMVar_hsa_circ_191663,RMVar_hsa_circ_191664,RMVar_hsa_circ_109409,RMVar_hsa_circ_97702,RMVar_hsa_circ_191668,RMVar_hsa_circ_191670,RMVar_hsa_circ_84269,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_43411,RMVar_hsa_circ_104087,RMVar_hsa_circ_17605,RMVar_hsa_circ_191677,RMVar_hsa_circ_126590,RMVar_hsa_circ_191675,RMVar_hsa_circ_116193,RMVar_hsa_circ_191676,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_373055,RMVar_hsa_circ_191680,RMVar_hsa_circ_114051,RMVar_hsa_circ_191679,RMVar_hsa_circ_279383,RMVar_hsa_circ_191681,RMVar_hsa_circ_41756 81165 RMVar_ID_81165 Human_SNP_ID_656671388 m1A Human chr19 + 5219281 5219276 5219281 CCTCCTTTTCCAGGAAGCCCTCCCTGCTGTCAAGTCAAGTCGGGGAGGACATGGGGCTTACTTCT CCTCCTTTTCCAGGAAGCCCTCCCTGCT_____GTCAAGTCGGGGAGGACATGGGGCTTACTTCT TGTCAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5219278..5219395 26863196 MeRIP-seq:(Medium) rs745915967 Functional Loss DEL dbSNP153 29..33 33 - - - 81166 RMVar_ID_81166 Human_SNP_ID_656671391 m1A Human chr19 + 5219281 5219281 5219281 CCTCCTTTTCCAGGAAGCCCTCCCTGCTGTCAAGTCAAGTCGGGGAGGACATGGGGCTTACTTCT CCTCCTTTTCCAGGAAGCCCTCCCTGCTGTCAGGTCAAGTCGGGGAGGACATGGGGCTTACTTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5219278..5219395 26863196 MeRIP-seq:(Medium) rs1406993272 Functional Loss SNV dbSNP153 33..33 33 - - - 81167 RMVar_ID_81167 Human_SNP_ID_656671663 m1A Human chr19 - 5220024 5220024 5220024 GCCACCCACGTTCCATCCCGGCGACCAGAAGCAGTATGGCGGCTTCGATAACCGGGGCCTGGAGC GCCACCCACGTTCCATCCCGGCGACCAGAAGCGGTATGGCGGCTTCGATAACCGGGGCCTGGAGC T C PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5219974..5220056 26863196 MeRIP-seq:(Medium) rs757700265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53309,Human_RBP_ID_22447192,Human_RBP_ID_26815039 Human_Splice_Rec_1941807,Human_Splice_Rec_1941881,Human_Splice_Rec_1941937,Human_Splice_Rec_1941999,Human_Splice_Rec_1942053,Human_Splice_Rec_1942079 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_84269,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_17605,RMVar_hsa_circ_3453,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_191680,RMVar_hsa_circ_279383,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_191685,RMVar_hsa_circ_96530,RMVar_hsa_circ_125623,RMVar_hsa_circ_191686,RMVar_hsa_circ_14695,RMVar_hsa_circ_191687,RMVar_hsa_circ_341630,RMVar_hsa_circ_298835,RMVar_hsa_circ_191688 81168 RMVar_ID_81168 Human_SNP_ID_656671664 m1A Human chr19 - 5220024 5220024 5220024 GCCACCCACGTTCCATCCCGGCGACCAGAAGCAGTATGGCGGCTTCGATAACCGGGGCCTGGAGC GCCACCCACGTTCCATCCCGGCGACCAGAAGCCGTATGGCGGCTTCGATAACCGGGGCCTGGAGC T G PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5219974..5220056 26863196 MeRIP-seq:(Medium) rs757700265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53309,Human_RBP_ID_22447192,Human_RBP_ID_26815039 Human_Splice_Rec_1941807,Human_Splice_Rec_1941881,Human_Splice_Rec_1941937,Human_Splice_Rec_1941999,Human_Splice_Rec_1942053,Human_Splice_Rec_1942079 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_84269,RMVar_hsa_circ_191669,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_17605,RMVar_hsa_circ_3453,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_191680,RMVar_hsa_circ_279383,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_191685,RMVar_hsa_circ_96530,RMVar_hsa_circ_125623,RMVar_hsa_circ_191686,RMVar_hsa_circ_14695,RMVar_hsa_circ_191687,RMVar_hsa_circ_341630,RMVar_hsa_circ_298835,RMVar_hsa_circ_191688 81169 RMVar_ID_81169 Human_SNP_ID_656672107 m1A Human chr19 - 5221096 5221096 5221096 CCAGCAGACGGTCACCGCCTGGACTGCCTTCAACCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA CCAGCAGACGGTCACCGCCTGGACTGCCTTCAGCCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA T C PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5221045..5221203 26863196 MeRIP-seq:(Medium) rs372506721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5443402,Human_RBP_ID_9292640,Human_RBP_ID_17930037,Human_RBP_ID_27470814 Human_Splice_Rec_1941803,Human_Splice_Rec_1941877,Human_Splice_Rec_1941933,Human_Splice_Rec_1941995,Human_Splice_Rec_1942049 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_17605,RMVar_hsa_circ_3453,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686,RMVar_hsa_circ_191687,RMVar_hsa_circ_341630,RMVar_hsa_circ_298835,RMVar_hsa_circ_191688 81170 RMVar_ID_81170 Human_SNP_ID_656672108 m1A Human chr19 - 5221096 5221096 5221096 CCAGCAGACGGTCACCGCCTGGACTGCCTTCAACCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA CCAGCAGACGGTCACCGCCTGGACTGCCTTCACCCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA T G PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5221045..5221203 26863196 MeRIP-seq:(Medium) rs372506721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5443402,Human_RBP_ID_9292640,Human_RBP_ID_17930037,Human_RBP_ID_27470814 Human_Splice_Rec_1941803,Human_Splice_Rec_1941877,Human_Splice_Rec_1941933,Human_Splice_Rec_1941995,Human_Splice_Rec_1942049 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_17605,RMVar_hsa_circ_3453,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686,RMVar_hsa_circ_191687,RMVar_hsa_circ_341630,RMVar_hsa_circ_298835,RMVar_hsa_circ_191688 81171 RMVar_ID_81171 Human_SNP_ID_656672682 m1A Human chr19 + 5222615 5222615 5222615 AGCAGAAAAGTGAGCACTTACCTGGGCAGGGGAGAGGGAGGGGGCTGGGGTGGGGGTGGGCGCAA AGCAGAAAAGTGAGCACTTACCTGGGCAGGGGGGAGGGAGGGGGCTGGGGTGGGGGTGGGCGCAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5222613..5222800 26863196 MeRIP-seq:(Medium) rs1317658614 Functional Loss SNV dbSNP153 33..33 33 - - - 81172 RMVar_ID_81172 Human_SNP_ID_656672717 m1A Human chr19 - 5222666 5222666 5222666 CGGGACCAAGGTAGGCGCGCGGCGACCCCTGCACCAGAGCCGGACCGGGCCTTGCGCCCACCCCC CGGGACCAAGGTAGGCGCGCGGCGACCCCTGCGCCAGAGCCGGACCGGGCCTTGCGCCCACCCCC T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5222617..5222818 26863196 MeRIP-seq:(Medium) rs1259419535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19088833 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686 81173 RMVar_ID_81173 Human_SNP_ID_656672718 m1A Human chr19 - 5222666 5222666 5222666 CGGGACCAAGGTAGGCGCGCGGCGACCCCTGCACCAGAGCCGGACCGGGCCTTGCGCCCACCCCC CGGGACCAAGGTAGGCGCGCGGCGACCCCTGCCCCAGAGCCGGACCGGGCCTTGCGCCCACCCCC T G PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5222617..5222818 26863196 MeRIP-seq:(Medium) rs1259419535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19088833 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686 81174 RMVar_ID_81174 Human_SNP_ID_656676108 m1A Human chr19 - 5231471 5231471 5231471 CAGCGTCCGCTACCGACCGCTGGGCTCAGAGGACCCGGAACCCAAGGAGGTGAACGGCATCCCCC CAGCGTCCGCTACCGACCGCTGGGCTCAGAGGGCCCGGAACCCAAGGAGGTGAACGGCATCCCCC T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:5231426..5231500 26863196 MeRIP-seq:(Medium) rs1372364043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2017086,Human_miRNA_ID_2571352,Human_miRNA_ID_3045089 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_116358,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686,RMVar_hsa_circ_268265,RMVar_hsa_circ_191690,RMVar_hsa_circ_48567 81175 RMVar_ID_81175 Human_SNP_ID_656689727 m1A Human chr19 + 5274302 5274302 5274302 CCTGACACACGAAAGAGGCCACACCCCCCGACACGCCGATCTGGTCCTTGGGTTCTTTGATAAAC CCTGACACACGAAAGAGGCCACACCCCCCGACGCGCCGATCTGGTCCTTGGGTTCTTTGATAAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5274251..5274350 32194978 MeRIP-seq:(Medium) rs1338995814 Functional Loss SNV dbSNP153 33..33 33 - - - 81176 RMVar_ID_81176 Human_SNP_ID_656699994 m1A Human chr19 - 5309070 5309070 5309070 TCCAGGCTCCCCTCAGTTCCCACTTGGCACTCACCTCCCACCTCCACACACTCTGAGCCCAGGGC TCCAGGCTCCCCTCAGTTCCCACTTGGCACTCGCCTCCCACCTCCACACACTCTGAGCCCAGGGC T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5309065..5309165 26863196 MeRIP-seq:(Medium) rs931289757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_97862,RMVar_hsa_circ_191697 81177 RMVar_ID_81177 Human_SNP_ID_656700007 m1A Human chr19 + 5309113 5309105 5309114 TGGGAACTGAGGGGAGCCTGGAAACCACCAAAAACTGGAGCTGGCAGCTCCGGGGGTGGAGAGAG TGGGAACTGAGGGGAGCCTGGAAAC_________CTGGAGCTGGCAGCTCCGGGGGTGGAGAGAG CCACCAAAAA C lnc-ZNRF4-5 RNACentral:URS0000D5AA35 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5309073..5309158 26863196 MeRIP-seq:(Medium) rs1251818479 Functional Loss DEL dbSNP153 26..34 33 - - - 81178 RMVar_ID_81178 Human_SNP_ID_656709150 m1A Human chr19 - 5340757 5340757 5340757 CCCGGCAGCCCGGCCGGCGCGCGCACGCCGCGAGCCGCTGGCGCTCGGGCTCCGCTCGGATCCCA CCCGGCAGCCCGGCCGGCGCGCGCACGCCGCGCGCCGCTGGCGCTCGGGCTCCGCTCGGATCCCA T G PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:5340711..5340804;chr19:5340716..5340814 26863196 MeRIP-seq:(Medium) rs1235095345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557140 Human_Splice_Rec_1941781 RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_97862,RMVar_hsa_circ_191697 81179 RMVar_ID_81179 Human_SNP_ID_656759352 m1A Human chr19 - 5524941 5524941 5524941 GGTTGAGTGGAGGTAAGGATGGATAGGCCTGTAGGTAGATGGTGGAGGAAAGGGTAGATGAGTGA GGTTGAGTGGAGGTAAGGATGGATAGGCCTGTGGGTAGATGGTGGAGGAAAGGGTAGATGAGTGA T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5524935..5525305 26863196 MeRIP-seq:(Medium) rs554549 Functional Loss SNV dbSNP153 33..33 33 - - - 81180 RMVar_ID_81180 Human_SNP_ID_656766595 m1A Human chr19 + 5548625 5548625 5548625 CAGGCCAGGCCATCGCATCCCCTGTGACTGGCACGTATACATCCAGATGGCCTGAAGTAACTGAA CAGGCCAGGCCATCGCATCCCCTGTGACTGGCGCGTATACATCCAGATGGCCTGAAGTAACTGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5548554..5548684 26863196 MeRIP-seq:(Medium) rs1223140901 Functional Loss SNV dbSNP153 33..33 33 - - - 81181 RMVar_ID_81181 Human_SNP_ID_656767090 m1A Human chr19 + 5550181 5550181 5550181 CTCCCCTCCTCGCCAGCCCAAGCTAAGTCCCAATTCTTCCTCAGCCTCTGCTCCTGCATCCTGTC CTCCCCTCCTCGCCAGCCCAAGCTAAGTCCCAGTTCTTCCTCAGCCTCTGCTCCTGCATCCTGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:5550130..5550237;chr19:5550109..5550219 26863196 MeRIP-seq:(Medium) rs1482988221 Functional Loss SNV dbSNP153 33..33 33 - - - 81182 RMVar_ID_81182 Human_SNP_ID_656767663 m1A Human chr19 - 5551667 5551667 5551667 TGTGGAGGAACGGATTGAGGACAAAAGAGGGTACGGGTTGGGCACCACAGGGTGGATGGCAAAAC TGTGGAGGAACGGATTGAGGACAAAAGAGGGTGCGGGTTGGGCACCACAGGGTGGATGGCAAAAC T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5551620..5551748 26863196 MeRIP-seq:(Medium) rs928619171 Functional Loss SNV dbSNP153 33..33 33 - - - 81183 RMVar_ID_81183 Human_SNP_ID_656767725 m1A Human chr19 - 5551901 5551901 5551901 AGCACGTGTGTTTTTGAGAATTATGCCGAGATAGGTAACAGATGAGGAAGAAATTTGTGCTTGAT AGCACGTGTGTTTTTGAGAATTATGCCGAGATGGGTAACAGATGAGGAAGAAATTTGTGCTTGAT T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5551851..5551975 26863196 MeRIP-seq:(Medium) rs966438081 Functional Loss SNV dbSNP153 33..33 33 - - - 81184 RMVar_ID_81184 Human_SNP_ID_656767727 m1A Human chr19 - 5551905 5551905 5551905 GGAAAGCACGTGTGTTTTTGAGAATTATGCCGAGATAGGTAACAGATGAGGAAGAAATTTGTGCT GGAAAGCACGTGTGTTTTTGAGAATTATGCCGGGATAGGTAACAGATGAGGAAGAAATTTGTGCT T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5551857..5551971 26863196 MeRIP-seq:(Medium) rs540056546 Functional Loss SNV dbSNP153 33..33 33 - - - 81185 RMVar_ID_81185 Human_SNP_ID_656771197 m1A Human chr19 - 5564949 5564947 5564949 GAACAGACTGTGATGGGGGGAGGGCTGGAGACAGGAGACCAGGGTGAGGTCCCAGTGAGCCATGC GAACAGACTGTGATGGGGGGAGGGCTGGAGAC__GAGACCAGGGTGAGGTCCCAGTGAGCCATGC CCT C TINCR Ensembl:ENSG00000223573 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5564946..5565049 26863196 MeRIP-seq:(Medium) rs935820665 Functional Loss DEL dbSNP153 33..34 33 - - - 81186 RMVar_ID_81186 Human_SNP_ID_656771289 m1A Human chr19 - 5565210 5565210 5565210 CAGCCTGTGCAAAGGCCCTGAGGCAGGACTGCACCTGGCATGTTGGAGGAACAGCGAGGAGGCCC CAGCCTGTGCAAAGGCCCTGAGGCAGGACTGCTCCTGGCATGTTGGAGGAACAGCGAGGAGGCCC T A TINCR Ensembl:ENSG00000223573 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5565207..5565331 26863196 MeRIP-seq:(Medium) rs1485759928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6783702,Human_RBP_ID_13508652 81187 RMVar_ID_81187 Human_SNP_ID_656771667 m1A Human chr19 + 5566620 5566620 5566620 CAGAGAGACAGAGAGAAAAACAGCAGAGACAGAGACAAATGGACAAAGAGACAGAGAGACAGGGA CAGAGAGACAGAGAGAAAAACAGCAGAGACAGGGACAAATGGACAAAGAGACAGAGAGACAGGGA A G lnc-SAFB-1 RNACentral:URS00008B6BDF lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5566618..5566713 26863196 MeRIP-seq:(Medium) rs1313183083 Functional Loss SNV dbSNP153 33..33 33 - - - 81188 RMVar_ID_81188 Human_SNP_ID_656772049 m1A Human chr19 - 5567875 5567875 5567875 GGGGCTGTCGCGCTGGAAGCGCTACCACATCAAGGTGCACCTGGCGGACGAGGCGCTGCTGCTAC GGGGCTGTCGCGCTGGAAGCGCTACCACATCAGGGTGCACCTGGCGGACGAGGCGCTGCTGCTAC T C TINCR Ensembl:ENSG00000223573 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5567698..5567976 26863196 MeRIP-seq:(Medium) rs1245276550 Functional Loss SNV dbSNP153 33..33 33 - - - 81189 RMVar_ID_81189 Human_SNP_ID_656777752 m1A Human chr19 + 5587298 5587298 5587298 GGTACGGGGGGGGATGAGGGTGTGGGTGAGGGACTCTGCTGCCCCGGTCCTGGCTGGCCACTCCG GGTACGGGGGGGGATGAGGGTGTGGGTGAGGGGCTCTGCTGCCCCGGTCCTGGCTGGCCACTCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5587247..5591317 32194978 MeRIP-seq:(Medium) rs565415217 Functional Loss SNV dbSNP153 33..33 33 - - - 81190 RMVar_ID_81190 Human_SNP_ID_656777927 m1A Human chr19 + 5587725 5587725 5587725 CACCTTACCCCGCCACTCCACCGCGGCTTGCCATGTGCCCCGGCCCCGAGGGCCCAGACAGGCCC CACCTTACCCCGCCACTCCACCGCGGCTTGCCGTGTGCCCCGGCCCCGAGGGCCCAGACAGGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5587138..5588000 26863196 MeRIP-seq:(Medium) rs1334556656 Functional Loss SNV dbSNP153 33..33 33 - - - 81191 RMVar_ID_81191 Human_SNP_ID_656777928 m1A Human chr19 - 5587726 5587726 5587726 GGGGCCTGTCTGGGCCCTCGGGGCCGGGGCACATGGCAAGCCGCGGTGGAGTGGCGGGGTAAGGT GGGGCCTGTCTGGGCCCTCGGGGCCGGGGCACGTGGCAAGCCGCGGTGGAGTGGCGGGGTAAGGT T C SAFB2 Ensembl:ENSG00000130254 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5587247..5588924 26863196 MeRIP-seq:(Medium) rs771915355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771549,Human_RBP_ID_3956054,Human_RBP_ID_5321306,Human_RBP_ID_22533307,Human_RBP_ID_25440658 Human_Splice_Rec_1942154,Human_Splice_Rec_1942155,Human_Splice_Rec_1942160,Human_Splice_Rec_1942161 Human_miRNA_ID_2658907 RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_79224,RMVar_hsa_circ_19085,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_191700 81192 RMVar_ID_81192 Human_SNP_ID_656778750 m1A Human chr19 + 5590214 5590214 5590214 AGCTGAATCAAACCTTGGGGACGTGCCTGGCCAGGCACCAACCTTTTCCCAGGTTAGGACAGATG AGCTGAATCAAACCTTGGGGACGTGCCTGGCCGGGCACCAACCTTTTCCCAGGTTAGGACAGATG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5590212..5590400 26863196 MeRIP-seq:(Medium) rs184636516 Functional Loss SNV dbSNP153 33..33 33 - - - 81193 RMVar_ID_81193 Human_SNP_ID_656779608 m1A Human chr19 - 5592754 5592754 5592754 ATCGAGACCGGGGCCAGTACCAGGACCACGCCATCGACAGGTCAGTGGTCTTGTCCCCTCCTTTA ATCGAGACCGGGGCCAGTACCAGGACCACGCCTTCGACAGGTCAGTGGTCTTGTCCCCTCCTTTA T A SAFB2 Ensembl:ENSG00000130254 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5591714..5592867 32194978 MeRIP-seq:(Medium) rs760148144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826354,Human_RBP_ID_9380145,Human_RBP_ID_18470699,Human_RBP_ID_18996176 Human_Splice_Rec_1942147,Human_Splice_Rec_1942165,Human_Splice_Rec_1942171 RMVar_hsa_circ_9276,RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_12752,RMVar_hsa_circ_265514,RMVar_hsa_circ_322463,RMVar_hsa_circ_11051 81194 RMVar_ID_81194 Human_SNP_ID_656779670 m1A Human chr19 - 5592866 5592866 5592866 AAAACCAACAGACGAGATGATGCCTATTGGCCAGAAGGAAAGCGTGTGGCAATGGAGGACCGATA AAAACCAACAGACGAGATGATGCCTATTGGCCGGAAGGAAAGCGTGTGGCAATGGAGGACCGATA T C SAFB2 Ensembl:ENSG00000130254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:5592817..5593895 32194978 MeRIP-seq:(Medium) rs760373908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53879,Human_RBP_ID_4547353,Human_RBP_ID_18470423,Human_RBP_ID_18996177 Human_Splice_Rec_1942146,Human_Splice_Rec_1942164 RMVar_hsa_circ_9276,RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_12752,RMVar_hsa_circ_265514,RMVar_hsa_circ_322463,RMVar_hsa_circ_11051 81195 RMVar_ID_81195 Human_SNP_ID_656781449 m1A Human chr19 + 5598821 5598821 5598821 TCACTCTCTCTTTGGACCTGCTTGTGGTTTTCACGCTAATGACGGGCTCTCCTTTCGATTTATCC TCACTCTCTCTTTGGACCTGCTTGTGGTTTTCCCGCTAATGACGGGCTCTCCTTTCGATTTATCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:5598809..5600205 32194978 MeRIP-seq:(Medium) rs982507765 Functional Loss SNV dbSNP153 33..33 33 - - - 81196 RMVar_ID_81196 Human_SNP_ID_656788669 m1A Human chr19 + 5623176 5623176 5623176 AGGAGCCTGATAAAACCGGCCCGGTTCTGTGGAAAGTGGGCGGCGGAGCCAGGGTCCCTGGAATG AGGAGCCTGATAAAACCGGCCCGGTTCTGTGGCAAGTGGGCGGCGGAGCCAGGGTCCCTGGAATG A C SAFB Ensembl:ENSG00000160633 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5623126..5623375 26863196 MeRIP-seq:(Medium) rs941978295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55440,Human_RBP_ID_1891943,Human_RBP_ID_3576629,Human_RBP_ID_4548293,Human_RBP_ID_8838971,Human_RBP_ID_9380165,Human_RBP_ID_18420837,Human_RBP_ID_18739626,Human_RBP_ID_22068575,Human_RBP_ID_23807693,Human_RBP_ID_26334785,Human_RBP_ID_26995668 81197 RMVar_ID_81197 Human_SNP_ID_656788773 m1A Human chr19 + 5623356 5623356 5623356 GGGCGGAGCTGAGGAAACGGAATGTGGACTCGAGCGGCAACAAGAGCGTTTTGATGGAGCGGCTG GGGCGGAGCTGAGGAAACGGAATGTGGACTCGGGCGGCAACAAGAGCGTTTTGATGGAGCGGCTG A G SAFB Ensembl:ENSG00000160633 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5623084..5641775 26863196 MeRIP-seq:(Medium) rs1192570312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55441,Human_RBP_ID_1891944,Human_RBP_ID_6784617,Human_RBP_ID_9380167,Human_RBP_ID_13512543,Human_RBP_ID_23119114,Human_RBP_ID_23807696,Human_RBP_ID_27814960 Human_Splice_Rec_1942231,Human_Splice_Rec_1942267,Human_Splice_Rec_1942273,Human_Splice_Rec_1942313,Human_Splice_Rec_1942353,Human_Splice_Rec_1942393,Human_Splice_Rec_1942409 81198 RMVar_ID_81198 Human_SNP_ID_656788775 m1A Human chr19 + 5623363 5623363 5623363 GCTGAGGAAACGGAATGTGGACTCGAGCGGCAACAAGAGCGTTTTGATGGAGCGGCTGAAGAAGG GCTGAGGAAACGGAATGTGGACTCGAGCGGCACCAAGAGCGTTTTGATGGAGCGGCTGAAGAAGG A C SAFB Ensembl:ENSG00000160633 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5623101..5641812 26863196 MeRIP-seq:(Medium) rs779942953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1891944,Human_RBP_ID_4548304,Human_RBP_ID_6784617,Human_RBP_ID_9380167,Human_RBP_ID_13512543,Human_RBP_ID_23114750,Human_RBP_ID_23119114,Human_RBP_ID_23807696,Human_RBP_ID_26335315,Human_RBP_ID_27814960 Human_Splice_Rec_1942231,Human_Splice_Rec_1942267,Human_Splice_Rec_1942273,Human_Splice_Rec_1942313,Human_Splice_Rec_1942353,Human_Splice_Rec_1942393,Human_Splice_Rec_1942409 81199 RMVar_ID_81199 Human_SNP_ID_656788776 m1A Human chr19 + 5623363 5623363 5623363 GCTGAGGAAACGGAATGTGGACTCGAGCGGCAACAAGAGCGTTTTGATGGAGCGGCTGAAGAAGG GCTGAGGAAACGGAATGTGGACTCGAGCGGCAGCAAGAGCGTTTTGATGGAGCGGCTGAAGAAGG A G SAFB Ensembl:ENSG00000160633 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5623101..5641812 26863196 MeRIP-seq:(Medium) rs779942953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1891944,Human_RBP_ID_4548304,Human_RBP_ID_6784617,Human_RBP_ID_9380167,Human_RBP_ID_13512543,Human_RBP_ID_23114750,Human_RBP_ID_23119114,Human_RBP_ID_23807696,Human_RBP_ID_26335315,Human_RBP_ID_27814960 Human_Splice_Rec_1942231,Human_Splice_Rec_1942267,Human_Splice_Rec_1942273,Human_Splice_Rec_1942313,Human_Splice_Rec_1942353,Human_Splice_Rec_1942393,Human_Splice_Rec_1942409 81200 RMVar_ID_81200 Human_SNP_ID_656793925 m1A Human chr19 - 5641561 5641561 5641561 CTGAAGACAGAATCATTTACAGCATGAGATCAAATGATACGCACTTTACAGAAGCAACAATGCCC CTGAAGACAGAATCATTTACAGCATGAGATCACATGATACGCACTTTACAGAAGCAACAATGCCC T G RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5641559..5641767 26863196 MeRIP-seq:(Medium) rs1231453184 Functional Loss SNV dbSNP153 33..33 33 - - - 81201 RMVar_ID_81201 Human_SNP_ID_656793954 m1A Human chr19 + 5641655 5641655 5641655 GATAACGGGCTGGAGGAAAACTCTGGGGATGGACAGGTATGTGCAGCCTTGCGAGTGAGTAGCGT GATAACGGGCTGGAGGAAAACTCTGGGGATGGTCAGGTATGTGCAGCCTTGCGAGTGAGTAGCGT A T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5623084..5641835 26863196 MeRIP-seq:(Medium) rs999517839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8162,Human_RBP_ID_825520,Human_RBP_ID_907174,Human_RBP_ID_5116011,Human_RBP_ID_5375323,Human_RBP_ID_6784740,Human_RBP_ID_9380173,Human_RBP_ID_23131810,Human_RBP_ID_24545559,Human_RBP_ID_26334787,Human_RBP_ID_27814962 Human_Splice_Rec_1942276,Human_Splice_Rec_1942277,Human_Splice_Rec_1942316,Human_Splice_Rec_1942317,Human_Splice_Rec_1942356,Human_Splice_Rec_1942357,Human_Splice_Rec_1942396,Human_Splice_Rec_1942397,Human_Splice_Rec_1942412,Human_Splice_Rec_1942413 RMVar_hsa_circ_62776,RMVar_hsa_circ_352713,RMVar_hsa_circ_366604,RMVar_hsa_circ_369070,RMVar_hsa_circ_359003,RMVar_hsa_circ_103308,RMVar_hsa_circ_284702,RMVar_hsa_circ_67164,RMVar_hsa_circ_191717,RMVar_hsa_circ_191718,RMVar_hsa_circ_191719 81202 RMVar_ID_81202 Human_SNP_ID_656797354 m1A Human chr19 + 5654123 5654123 5654123 TGACAGAAAAGATGATGCTAAGAAGGGTGACGACGGAAGTGGAGAAAAGAGTAAGGACCAAGATG TGACAGAAAAGATGATGCTAAGAAGGGTGACGGCGGAAGTGGAGAAAAGAGTAAGGACCAAGATG A G SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5654046..5654231 26863196 MeRIP-seq:(Medium) rs1203017645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067435,Human_RBP_ID_1571508,Human_RBP_ID_1892005,Human_RBP_ID_4548352,Human_RBP_ID_5585919,Human_RBP_ID_6784946,Human_RBP_ID_8494237,Human_RBP_ID_8837296,Human_RBP_ID_9258943,Human_RBP_ID_9380182,Human_RBP_ID_13513598,Human_RBP_ID_22979852,Human_RBP_ID_26334790,Human_RBP_ID_27814966 Human_Splice_Rec_1942248,Human_Splice_Rec_1942249,Human_Splice_Rec_1942294,Human_Splice_Rec_1942295,Human_Splice_Rec_1942334,Human_Splice_Rec_1942335,Human_Splice_Rec_1942374,Human_Splice_Rec_1942375,Human_Splice_Rec_1942428,Human_Splice_Rec_1942429 RMVar_hsa_circ_478,RMVar_hsa_circ_352713,RMVar_hsa_circ_359003,RMVar_hsa_circ_65883,RMVar_hsa_circ_72641,RMVar_hsa_circ_330450,RMVar_hsa_circ_92292,RMVar_hsa_circ_191722,RMVar_hsa_circ_191721,RMVar_hsa_circ_322122,RMVar_hsa_circ_331764,RMVar_hsa_circ_274975,RMVar_hsa_circ_271748,RMVar_hsa_circ_191724,RMVar_hsa_circ_191726,RMVar_hsa_circ_35510,RMVar_hsa_circ_191727,RMVar_hsa_circ_191725,RMVar_hsa_circ_191728,RMVar_hsa_circ_191729,RMVar_hsa_circ_270892 81203 RMVar_ID_81203 Human_SNP_ID_656799817 m1A Human chr19 + 5661656 5661656 5661656 CAGCGGCTGGAGCGGGAGCGCATGGAGCGGGAACGGCTGGAGCGCGAACGCATGCACGTGGAGCA CAGCGGCTGGAGCGGGAGCGCATGGAGCGGGAGCGGCTGGAGCGCGAACGCATGCACGTGGAGCA A G SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5657201..5661805 26863196 MeRIP-seq:(Medium) rs1235416930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910360,Human_RBP_ID_3956065,Human_RBP_ID_8837307,Human_RBP_ID_9294106,Human_RBP_ID_9380185,Human_RBP_ID_13514064,Human_RBP_ID_18412260,Human_RBP_ID_18470700,Human_RBP_ID_22447199,Human_RBP_ID_22977373,Human_RBP_ID_26335336,Human_RBP_ID_27814968 RMVar_hsa_circ_35510,RMVar_hsa_circ_191727,RMVar_hsa_circ_48528,RMVar_hsa_circ_368479 81204 RMVar_ID_81204 Human_SNP_ID_656800758 m1A Human chr19 + 5664436 5664436 5664436 GGTTCAAGGTCAATGATGGGAGAACGAGAAGGACAGGTAAGTCTGAAGCTACAGTGGTAGCCACA GGTTCAAGGTCAATGATGGGAGAACGAGAAGGTCAGGTAAGTCTGAAGCTACAGTGGTAGCCACA A T SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:5663986..5664481;chr19:5663987..5664461;chr19:5663971..5664461;chr19:5663973..5664461 26863196 MeRIP-seq:(Medium) rs555519359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910361,Human_RBP_ID_1571554,Human_RBP_ID_1892025,Human_RBP_ID_5372938,Human_RBP_ID_6785124,Human_RBP_ID_13514237,Human_RBP_ID_18996189,Human_RBP_ID_19088850,Human_RBP_ID_22661840 Human_Splice_Rec_1942258,Human_Splice_Rec_1942259,Human_Splice_Rec_1942304,Human_Splice_Rec_1942305,Human_Splice_Rec_1942344,Human_Splice_Rec_1942345,Human_Splice_Rec_1942384,Human_Splice_Rec_1942385,Human_Splice_Rec_1942438,Human_Splice_Rec_1942439,Human_Splice_Rec_1942468 RMVar_hsa_circ_320807 81205 RMVar_ID_81205 Human_SNP_ID_656801324 m1A Human chr19 - 5666823 5666823 5666823 CATGGCCTGGTACAAAAAAGGTACTAGTACCAAGGCATCTCCAAGGCAGGTCCCCACAGCACCAC CATGGCCTGGTACAAAAAAGGTACTAGTACCAGGGCATCTCCAAGGCAGGTCCCCACAGCACCAC T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5666788..5666906 32194978 MeRIP-seq:(Medium) rs1414104487 Functional Loss SNV dbSNP153 33..33 33 - - - 81206 RMVar_ID_81206 Human_SNP_ID_656801430 m1A Human chr19 + 5667122 5667122 5667122 CTCCCGCGATGGCTGGGGGGGCTATGGCTCTGACAAGAGGATGAGCGAGGGCCGGGGGCTGCCTC CTCCCGCGATGGCTGGGGGGGCTATGGCTCTGTCAAGAGGATGAGCGAGGGCCGGGGGCTGCCTC A T SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5666998..5667205 26863196 MeRIP-seq:(Medium) rs779032031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55451,Human_RBP_ID_3954251,Human_RBP_ID_8494331,Human_RBP_ID_8838979,Human_RBP_ID_9294107,Human_RBP_ID_13514682,Human_RBP_ID_17931294,Human_RBP_ID_18996191 Human_Splice_Rec_1942260,Human_Splice_Rec_1942261,Human_Splice_Rec_1942306,Human_Splice_Rec_1942307,Human_Splice_Rec_1942346,Human_Splice_Rec_1942347,Human_Splice_Rec_1942386,Human_Splice_Rec_1942387,Human_Splice_Rec_1942440,Human_Splice_Rec_1942441,Human_Splice_Rec_1942471 RMVar_hsa_circ_320807 81207 RMVar_ID_81207 Human_SNP_ID_656801443 m1A Human chr19 - 5667153 5667153 5667153 TGTCGGGTGTGGGACACAAACCTGGGGGGAGGAGGCAGCCCCCGGCCCTCGCTCATCCTCTTGTC TGTCGGGTGTGGGACACAAACCTGGGGGGAGGGGGCAGCCCCCGGCCCTCGCTCATCCTCTTGTC T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5667104..5667255 32194978 MeRIP-seq:(Medium) rs1007213475 Functional Loss SNV dbSNP153 33..33 33 - - - 81208 RMVar_ID_81208 Human_SNP_ID_656801574 m1A Human chr19 + 5667412 5667412 5667412 AGAGGATGACCGGTCATGGCAGGGCACGGCCGACGGGGGCATGATGGACAGGGATCACAAGAGGT AGAGGATGACCGGTCATGGCAGGGCACGGCCGCCGGGGGCATGATGGACAGGGATCACAAGAGGT A C SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:5667291..5667504;chr19:5667010..5667504;chr19:5667304..5667554;chr19:5666996..5667504 26863196 MeRIP-seq:(Medium) rs1466892323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8164,Human_RBP_ID_55452,Human_RBP_ID_3954252,Human_RBP_ID_5372940,Human_RBP_ID_6785216,Human_RBP_ID_18442005,Human_RBP_ID_18739767,Human_RBP_ID_22664631,Human_RBP_ID_22977375,Human_RBP_ID_26335338,Human_RBP_ID_27839227 Human_Splice_Rec_1942262,Human_Splice_Rec_1942263,Human_Splice_Rec_1942308,Human_Splice_Rec_1942309,Human_Splice_Rec_1942348,Human_Splice_Rec_1942349,Human_Splice_Rec_1942388,Human_Splice_Rec_1942389,Human_Splice_Rec_1942442,Human_Splice_Rec_1942443,Human_Splice_Rec_1942472 Human_miRNA_ID_976268 81209 RMVar_ID_81209 Human_SNP_ID_656801733 m1A Human chr19 + 5667875 5667875 5667875 CACTCCGGGCCTGGCCACATGATGAACCGAGGAGGAATGTCAGGGTAAGGCATGCTGGGGGCGGC CACTCCGGGCCTGGCCACATGATGAACCGAGGGGGAATGTCAGGGTAAGGCATGCTGGGGGCGGC A G SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5667784..5667900 26863196 MeRIP-seq:(Medium) rs773456914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3956069,Human_RBP_ID_5375333,Human_RBP_ID_13514707,Human_RBP_ID_18442006,Human_RBP_ID_18994135,Human_RBP_ID_19088854 Human_Splice_Rec_1942264,Human_Splice_Rec_1942265,Human_Splice_Rec_1942310,Human_Splice_Rec_1942311,Human_Splice_Rec_1942350,Human_Splice_Rec_1942351,Human_Splice_Rec_1942390,Human_Splice_Rec_1942391,Human_Splice_Rec_1942444,Human_Splice_Rec_1942445,Human_Splice_Rec_1942469,Human_Splice_Rec_1942473 81210 RMVar_ID_81210 Human_SNP_ID_656801869 m1A Human chr19 + 5668220 5668220 5668220 CCTCCCGGGGCCACCCCATCCCACACGGTGGCATGCAGGGCGGGTTTGGAGGCCAGAGCCGGGGG CCTCCCGGGGCCACCCCATCCCACACGGTGGCGTGCAGGGCGGGTTTGGAGGCCAGAGCCGGGGG A G SAFB Ensembl:ENSG00000160633 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5667801..5668250 26863196 MeRIP-seq:(Medium) rs1231570592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54301,Human_RBP_ID_6785221,Human_RBP_ID_13514720,Human_RBP_ID_17656634,Human_RBP_ID_22446346 Human_Splice_Rec_1942266,Human_Splice_Rec_1942312,Human_Splice_Rec_1942352,Human_Splice_Rec_1942392,Human_Splice_Rec_1942446,Human_Splice_Rec_1942470,Human_Splice_Rec_1942474 Human_miRNA_ID_2381470,Human_miRNA_ID_3024479 RMVar_hsa_circ_109198,RMVar_hsa_circ_191730 81211 RMVar_ID_81211 Human_SNP_ID_656804770 m1A Human chr19 - 5678473 5678473 5678473 CCACTGACCTGAAGACTCCGGACTGGGACCCCACTCCGAGGGCAGCTCCCGGCCTTGCCGGCCCA CCACTGACCTGAAGACTCCGGACTGGGACCCCTCTCCGAGGGCAGCTCCCGGCCTTGCCGGCCCA T A MICOS13 Ensembl:ENSG00000174917 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:5678426..5678681;chr19:5678426..5678696;chr19:5678426..5678625 26863196 MeRIP-seq:(Medium) rs1483971032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527361,Human_RBP_ID_1571629,Human_RBP_ID_4548574,Human_RBP_ID_5194290,Human_RBP_ID_5443473,Human_RBP_ID_17655830 Human_miRNA_ID_95679,Human_miRNA_ID_1419325,Human_miRNA_ID_2242352 RMVar_hsa_circ_88213,RMVar_hsa_circ_105124,RMVar_hsa_circ_191731,RMVar_hsa_circ_191732 81212 RMVar_ID_81212 Human_SNP_ID_656804852 m1A Human chr19 - 5678634 5678634 5678634 GCCGTCCCTTTCCCACAGGCATCATGACGGTGATGTCAGCTCTGTCGGTGGCCCCCTCCAAGGCC GCCGTCCCTTTCCCACAGGCATCATGACGGTGCTGTCAGCTCTGTCGGTGGCCCCCTCCAAGGCC T G MICOS13 Ensembl:ENSG00000174917 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5678420..5678840 32194978 MeRIP-seq:(Medium) rs1478019928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910365,Human_RBP_ID_9089758,Human_RBP_ID_17655833,Human_RBP_ID_22448213,Human_RBP_ID_22661845,Human_RBP_ID_22762693,Human_RBP_ID_25434775,Human_RBP_ID_26815044 Human_Splice_Rec_1942520,Human_Splice_Rec_1942526,Human_Splice_Rec_1942532 RMVar_hsa_circ_88213,RMVar_hsa_circ_105124,RMVar_hsa_circ_191731,RMVar_hsa_circ_191732 81213 RMVar_ID_81213 Human_SNP_ID_656805398 m1A Human chr19 + 5680157 5680157 5680157 CTCCGAGCACGCATTCACTTCTCATCCACGCCAGCGGCAGGATTCACCGGCATTCCCACCTCACA CTCCGAGCACGCATTCACTTCTCATCCACGCCGGCGGCAGGATTCACCGGCATTCCCACCTCACA A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5680154..5680555 32194978 MeRIP-seq:(Medium) rs770932511 Functional Loss SNV dbSNP153 33..33 33 - - - 81214 RMVar_ID_81214 Human_SNP_ID_656806167 m1A Human chr19 - 5682299 5682299 5682299 TTGGTCTCCCCCACCTCCACACTGGCTTCCCCATGTCCATACTCATTCTCTCCCTGCCTCTTCTG TTGGTCTCCCCCACCTCCACACTGGCTTCCCCGTGTCCATACTCATTCTCTCCCTGCCTCTTCTG T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5682289..5682535 26863196 MeRIP-seq:(Medium) rs1416718375 Functional Loss SNV dbSNP153 33..33 33 - - - 81215 RMVar_ID_81215 Human_SNP_ID_656806945 m1A Human chr19 - 5685016 5685016 5685016 GCTCCTCACCAACACCAGCGTTGGCCCCTGTCAGCAGCACTCGCGCTCCCTGGAGGCTGGCTGGC GCTCCTCACCAACACCAGCGTTGGCCCCTGTCGGCAGCACTCGCGCTCCCTGGAGGCTGGCTGGC T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5681101..5685109 32194978 MeRIP-seq:(Medium) rs1010641243 Functional Loss SNV dbSNP153 33..33 33 - - - 81216 RMVar_ID_81216 Human_SNP_ID_656808835 m1A Human chr19 + 5690323 5690323 5690323 CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCCGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC A C RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:5690201..5691734;chr19:5690201..5690691 26863196 MeRIP-seq:(Medium) rs1031184108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241570,Human_RBP_ID_527393,Human_RBP_ID_773875,Human_RBP_ID_908349,Human_RBP_ID_1571660,Human_RBP_ID_4557143,Human_RBP_ID_9328492,Human_RBP_ID_17655836,Human_RBP_ID_17931389,Human_RBP_ID_19091781,Human_RBP_ID_22533094,Human_RBP_ID_22590912,Human_RBP_ID_26815050 Human_Splice_Rec_1942477,Human_Splice_Rec_1942489,Human_Splice_Rec_1942495,Human_Splice_Rec_1942499,Human_Splice_Rec_1942505,Human_Splice_Rec_1942507 81217 RMVar_ID_81217 Human_SNP_ID_656808836 m1A Human chr19 + 5690323 5690323 5690323 CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCGGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:5690201..5691734;chr19:5690201..5690691 26863196 MeRIP-seq:(Medium) rs1031184108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241570,Human_RBP_ID_527393,Human_RBP_ID_773875,Human_RBP_ID_908349,Human_RBP_ID_1571660,Human_RBP_ID_4557143,Human_RBP_ID_9328492,Human_RBP_ID_17655836,Human_RBP_ID_17931389,Human_RBP_ID_19091781,Human_RBP_ID_22533094,Human_RBP_ID_22590912,Human_RBP_ID_26815050 Human_Splice_Rec_1942477,Human_Splice_Rec_1942489,Human_Splice_Rec_1942495,Human_Splice_Rec_1942499,Human_Splice_Rec_1942505,Human_Splice_Rec_1942507 81218 RMVar_ID_81218 Human_SNP_ID_656808837 m1A Human chr19 + 5690323 5690323 5690323 CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC CAGCCCTTCCGCCACGGCCGTCTCTGGAGAGCTGCAGGTAAGTGGTTTCCCGCACTGCCGGTATC A T RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:5690201..5691734;chr19:5690201..5690691 26863196 MeRIP-seq:(Medium) rs1031184108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241570,Human_RBP_ID_527393,Human_RBP_ID_773875,Human_RBP_ID_908349,Human_RBP_ID_1571660,Human_RBP_ID_4557143,Human_RBP_ID_9328492,Human_RBP_ID_17655836,Human_RBP_ID_17931389,Human_RBP_ID_19091781,Human_RBP_ID_22533094,Human_RBP_ID_22590912,Human_RBP_ID_26815050 Human_Splice_Rec_1942477,Human_Splice_Rec_1942489,Human_Splice_Rec_1942495,Human_Splice_Rec_1942499,Human_Splice_Rec_1942505,Human_Splice_Rec_1942507 81219 RMVar_ID_81219 Human_SNP_ID_656808840 m1A Human chr19 + 5690326 5690326 5690326 CCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCAGGTAAGTGGTTTCCCGCACTGCCGGTATCCGC CCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCCGGTAAGTGGTTTCCCGCACTGCCGGTATCCGC A C RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:5690276..5690443 26863196 MeRIP-seq:(Medium) rs892599722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241570,Human_RBP_ID_773875,Human_RBP_ID_908349,Human_RBP_ID_4557143,Human_RBP_ID_9328492,Human_RBP_ID_17655836,Human_RBP_ID_19091781,Human_RBP_ID_22533094,Human_RBP_ID_26815051 Human_Splice_Rec_1942477,Human_Splice_Rec_1942489,Human_Splice_Rec_1942495,Human_Splice_Rec_1942499,Human_Splice_Rec_1942505,Human_Splice_Rec_1942507 81220 RMVar_ID_81220 Human_SNP_ID_656808841 m1A Human chr19 + 5690326 5690326 5690326 CCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCAGGTAAGTGGTTTCCCGCACTGCCGGTATCCGC CCCTTCCGCCACGGCCGTCTCTGGAGAGCAGCGGGTAAGTGGTTTCCCGCACTGCCGGTATCCGC A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:5690276..5690443 26863196 MeRIP-seq:(Medium) rs892599722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241570,Human_RBP_ID_773875,Human_RBP_ID_908349,Human_RBP_ID_4557143,Human_RBP_ID_9328492,Human_RBP_ID_17655836,Human_RBP_ID_19091781,Human_RBP_ID_22533094,Human_RBP_ID_26815051 Human_Splice_Rec_1942477,Human_Splice_Rec_1942489,Human_Splice_Rec_1942495,Human_Splice_Rec_1942499,Human_Splice_Rec_1942505,Human_Splice_Rec_1942507 81221 RMVar_ID_81221 Human_SNP_ID_656808924 m1A Human chr19 + 5690516 5690516 5690516 TTCTCCCCGTCGCTGTCCGCAGCCATGGCCCTACGCTACCCTATGGCCGTGGGCCTCAACAAGGG TTCTCCCCGTCGCTGTCCGCAGCCATGGCCCTGCGCTACCCTATGGCCGTGGGCCTCAACAAGGG A G RPL36 Ensembl:ENSG00000130255 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:5690504..5690597 26863410 MeRIP-seq:(Medium) rs1385750157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53897,Human_RBP_ID_240205,Human_RBP_ID_527396,Human_RBP_ID_771561,Human_RBP_ID_826484,Human_RBP_ID_910367,Human_RBP_ID_1018190,Human_RBP_ID_1191679,Human_RBP_ID_1571663,Human_RBP_ID_3576846,Human_RBP_ID_4548677,Human_RBP_ID_8494414,Human_RBP_ID_9089788,Human_RBP_ID_17655838,Human_RBP_ID_18191875,Human_RBP_ID_18739860,Human_RBP_ID_19088857,Human_RBP_ID_22239578,Human_RBP_ID_22448215,Human_RBP_ID_22533095,Human_RBP_ID_22812433,Human_RBP_ID_23807941,Human_RBP_ID_26470382,Human_RBP_ID_26815054,Human_RBP_ID_26995798,Human_RBP_ID_27278681 Human_Splice_Rec_1942478,Human_Splice_Rec_1942479,Human_Splice_Rec_1942490,Human_Splice_Rec_1942491,Human_Splice_Rec_1942496,Human_Splice_Rec_1942497,Human_Splice_Rec_1942500,Human_Splice_Rec_1942501,Human_Splice_Rec_1942506,Human_Splice_Rec_1942508,Human_Splice_Rec_1942509,Human_Splice_Rec_1942511 Human_miRNA_ID_2009016,Human_miRNA_ID_2009017,Human_miRNA_ID_2009018 RMVar_hsa_circ_107324,RMVar_hsa_circ_123924,RMVar_hsa_circ_191733,RMVar_hsa_circ_191734 81222 RMVar_ID_81222 Human_SNP_ID_656809186 m1A Human chr19 + 5691218 5691218 5691218 GTTAATACCTTGGTTCTCACAGCTACCCACAGAGGGGAGGAAGTAGCCAGGGAAATCGCGGCAGC GTTAATACCTTGGTTCTCACAGCTACCCACAGGGGGGAGGAAGTAGCCAGGGAAATCGCGGCAGC A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:5691216..5691565 26863196 MeRIP-seq:(Medium) rs967736209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22976338 RMVar_hsa_circ_107324,RMVar_hsa_circ_123924,RMVar_hsa_circ_191733,RMVar_hsa_circ_191734 81223 RMVar_ID_81223 Human_SNP_ID_656809194 m1A Human chr19 + 5691239 5691239 5691239 GCTACCCACAGAGGGGAGGAAGTAGCCAGGGAAATCGCGGCAGCGCGAGAGAAGCTGCTTAACTA GCTACCCACAGAGGGGAGGAAGTAGCCAGGGAGATCGCGGCAGCGCGAGAGAAGCTGCTTAACTA A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:5691234..5691541 26863196 MeRIP-seq:(Medium) rs918053928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824932,Human_RBP_ID_3583099 RMVar_hsa_circ_107324,RMVar_hsa_circ_123924,RMVar_hsa_circ_191733,RMVar_hsa_circ_191734 81224 RMVar_ID_81224 Human_SNP_ID_656809211 m1A Human chr19 + 5691278 5691278 5691278 GCAGCGCGAGAGAAGCTGCTTAACTAGAATGCAGGGATCCCCCTACCCTGACGGCCGCCCCTTTC GCAGCGCGAGAGAAGCTGCTTAACTAGAATGCGGGGATCCCCCTACCCTGACGGCCGCCCCTTTC A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:5691274..5691730;chr19:5691275..5691675 26863196 MeRIP-seq:(Medium) rs748826847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22590914,Human_RBP_ID_22976340 RMVar_hsa_circ_107324,RMVar_hsa_circ_123924,RMVar_hsa_circ_191733,RMVar_hsa_circ_191734 81225 RMVar_ID_81225 Human_SNP_ID_656809627 m1A Human chr19 - 5691981 5691981 5691981 AGGCGGCGGATGTCAGGCCCTGTCTGGGCCAGAACTGAGCGCTGTGGGGAGCGCGCCCGGACCTG AGGCGGCGGATGTCAGGCCCTGTCTGGGCCAGCACTGAGCGCTGTGGGGAGCGCGCCCGGACCTG T G LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5691931..5692225 26863196 MeRIP-seq:(Medium) rs1345579745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4548735,Human_RBP_ID_5117286,Human_RBP_ID_5144976,Human_RBP_ID_5238605,Human_RBP_ID_17655305,Human_RBP_ID_18739883,Human_RBP_ID_23808021,Human_RBP_ID_27278696 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_110522,RMVar_hsa_circ_191737 81226 RMVar_ID_81226 Human_SNP_ID_656810440 m1A Human chr19 + 5693559 5693559 5693559 AGGTGGGAGCGGATGGCGCGGTCACCTCGGGCACATGCAGGTGGATGTGTGAGGTCACCAGGTAG AGGTGGGAGCGGATGGCGCGGTCACCTCGGGCGCATGCAGGTGGATGTGTGAGGTCACCAGGTAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:5693551..5693600 26863196 MeRIP-seq:(Medium) rs754069779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571743,Human_RBP_ID_18739921,Human_RBP_ID_22503773,Human_RBP_ID_22812471 81227 RMVar_ID_81227 Human_SNP_ID_656810516 m1A Human chr19 + 5693717 5693717 5693717 ACCTCCAGGCTGCCATCCTTGTCACCCTTGGCATCCTTGTCCTGTGGCCGTCTCAGGGATGTCTC ACCTCCAGGCTGCCATCCTTGTCACCCTTGGCGTCCTTGTCCTGTGGCCGTCTCAGGGATGTCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5693259..5693785 26863196 MeRIP-seq:(Medium) rs137990308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571749,Human_RBP_ID_8494464,Human_RBP_ID_22812472 81228 RMVar_ID_81228 Human_SNP_ID_656811088 m1A Human chr19 - 5694839 5694839 5694839 TGTGGCTTGGATGAGAGCAAGGCCAAGCTGTCATCGGACGTGCTGACGCTGCTCATCAAGCAGTA TGTGGCTTGGATGAGAGCAAGGCCAAGCTGTCGTCGGACGTGCTGACGCTGCTCATCAAGCAGTA T C LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5694762..5694878 26863196 MeRIP-seq:(Medium) rs373301964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1892102,Human_RBP_ID_8837342,Human_RBP_ID_26815075 Human_Splice_Rec_1942802,Human_Splice_Rec_1942803,Human_Splice_Rec_1942836,Human_Splice_Rec_1942837,Human_Splice_Rec_1942870,Human_Splice_Rec_1942871,Human_Splice_Rec_1942906,Human_Splice_Rec_1942907,Human_Splice_Rec_1942940,Human_Splice_Rec_1942941,Human_Splice_Rec_1942974,Human_Splice_Rec_1942975,Human_Splice_Rec_1943008,Human_Splice_Rec_1943009 Human_miRNA_ID_2757121 RMVar_hsa_circ_97269,RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_110522,RMVar_hsa_circ_191737,RMVar_hsa_circ_191739 81229 RMVar_ID_81229 Human_SNP_ID_656816667 m1A Human chr19 + 5707015 5707015 5707015 GCTCCAGAGCCTGACTGATGTCACGTGGCCCGAGGGGAAGGCCCCCAAGAGTGGCTGCGCCTCAG GCTCCAGAGCCTGACTGATGTCACGTGGCCCGCGGGGAAGGCCCCCAAGAGTGGCTGCGCCTCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5707009..5707187 26863196 MeRIP-seq:(Medium) rs750459898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571988 81230 RMVar_ID_81230 Human_SNP_ID_656817115 m1A Human chr19 + 5707984 5707984 5707984 TCGCTGGGAGCCAGCTCTGCTGCTTGTTCTCCAGAGTTCAGGGCCCACCCGTCCTGGGCTGGAAA TCGCTGGGAGCCAGCTCTGCTGCTTGTTCTCCGGAGTTCAGGGCCCACCCGTCCTGGGCTGGAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5707973..5708167 26863196 MeRIP-seq:(Medium) rs1369070208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1572002,Human_RBP_ID_18740066,Human_RBP_ID_22812563 81231 RMVar_ID_81231 Human_SNP_ID_656817224 m1A Human chr19 + 5708330 5708328 5708330 GCAGAGATGCCCCCGCCTGGCCAGCTGCCCGCACAGAGGCCCACCTGTAGAGAGGGTTCAAGGCA GCAGAGATGCCCCCGCCTGGCCAGCTGCCCG__CAGAGGCCCACCTGTAGAGAGGGTTCAAGGCA GCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5708326..5708449 32194978 MeRIP-seq:(Medium) rs1264749673 Functional Loss DEL dbSNP153 32..33 33 - - - 81232 RMVar_ID_81232 Human_SNP_ID_656817255 m1A Human chr19 - 5708405 5708405 5708405 CTGGGCCCCAGCGACCCTGCCCCATACTTGGCAGGCCCTGACTGCAGAGATCGTGAAGACCATCC CTGGGCCCCAGCGACCCTGCCCCATACTTGGCTGGCCCTGACTGCAGAGATCGTGAAGACCATCC T A LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:5708326..5708425 26863196 MeRIP-seq:(Medium) rs760275177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13516044,Human_RBP_ID_18740074,Human_RBP_ID_22545479 Human_Splice_Rec_1942787,Human_Splice_Rec_1942819,Human_Splice_Rec_1942853,Human_Splice_Rec_1942889,Human_Splice_Rec_1942923,Human_Splice_Rec_1942957,Human_Splice_Rec_1942991,Human_Splice_Rec_1943043,Human_Splice_Rec_1943053 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747,RMVar_hsa_circ_364585,RMVar_hsa_circ_343012,RMVar_hsa_circ_300800,RMVar_hsa_circ_191749,RMVar_hsa_circ_191750,RMVar_hsa_circ_347834 81233 RMVar_ID_81233 Human_SNP_ID_656818516 m1A Human chr19 - 5711946 5711946 5711946 GGTGGAGCCCGAGGAGCCGGAGGCGGAGAACAAGCACAAGCCCCGCAGGAAGTCAAAGCGGGGCA GGTGGAGCCCGAGGAGCCGGAGGCGGAGAACAGGCACAAGCCCCGCAGGAAGTCAAAGCGGGGCA T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:5711846..5711975 26863410 MeRIP-seq:(Medium) rs1170447349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825980,Human_RBP_ID_18412468,Human_RBP_ID_18996212,Human_RBP_ID_23309988,Human_RBP_ID_26335356,Human_RBP_ID_27814974 Human_Splice_Rec_1942816,Human_Splice_Rec_1942886,Human_Splice_Rec_1942920,Human_Splice_Rec_1942954,Human_Splice_Rec_1942988,Human_Splice_Rec_1943050 Human_miRNA_ID_2237745,Human_miRNA_ID_3066347 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747,RMVar_hsa_circ_364585,RMVar_hsa_circ_343012,RMVar_hsa_circ_300800,RMVar_hsa_circ_339739,RMVar_hsa_circ_191749,RMVar_hsa_circ_191750,RMVar_hsa_circ_347834,RMVar_hsa_circ_191751,RMVar_hsa_circ_333482 81234 RMVar_ID_81234 Human_SNP_ID_656819182 m1A Human chr19 - 5714197 5714197 5714197 CGTCTCGCCCAGCCTTATGTCGGCGTCTTTCTAAAGAGAGATGACAGGTAAGTGTGATTTTTCCT CGTCTCGCCCAGCCTTATGTCGGCGTCTTTCTGAAGAGAGATGACAGGTAAGTGTGATTTTTCCT T C LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5714176..5714200 26863196 MeRIP-seq:(Medium) rs779175035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527524,Human_RBP_ID_9089856,Human_RBP_ID_18994145,Human_RBP_ID_24375318 Human_Splice_Rec_1942782,Human_Splice_Rec_1942783,Human_Splice_Rec_1942812,Human_Splice_Rec_1942813,Human_Splice_Rec_1942846,Human_Splice_Rec_1942847,Human_Splice_Rec_1942882,Human_Splice_Rec_1942883,Human_Splice_Rec_1942916,Human_Splice_Rec_1942917,Human_Splice_Rec_1942950,Human_Splice_Rec_1942951,Human_Splice_Rec_1942984,Human_Splice_Rec_1942985 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747,RMVar_hsa_circ_364585,RMVar_hsa_circ_191750,RMVar_hsa_circ_333482,RMVar_hsa_circ_294331,RMVar_hsa_circ_191752 81235 RMVar_ID_81235 Human_SNP_ID_656820816 m1A Human chr19 - 5718794 5718794 5718794 TTGGGGGTGGGGAGGGAGCAGGATGATGTAATAGAGAGAAAGCAGTGAGTGTAAGGAACTTGAGC TTGGGGGTGGGGAGGGAGCAGGATGATGTAATGGAGAGAAAGCAGTGAGTGTAAGGAACTTGAGC T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5718792..5718906 26863196 MeRIP-seq:(Medium) rs1164335685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1094400,Human_RBP_ID_6806130,Human_RBP_ID_13516670 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 81236 RMVar_ID_81236 Human_SNP_ID_656821210 m1A Human chr19 + 5719951 5719951 5719951 TCGCTTCCCAAAACCCCCGCCATTGGCCCCCAATTGCCGGGCCTCGGCCCCACAGTGCCCAAGGA TCGCTTCCCAAAACCCCCGCCATTGGCCCCCACTTGCCGGGCCTCGGCCCCACAGTGCCCAAGGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:5719809..5720150 26863196 MeRIP-seq:(Medium) rs953392115 Functional Loss SNV dbSNP153 33..33 33 - - - 81237 RMVar_ID_81237 Human_SNP_ID_656821211 m1A Human chr19 + 5719951 5719951 5719951 TCGCTTCCCAAAACCCCCGCCATTGGCCCCCAATTGCCGGGCCTCGGCCCCACAGTGCCCAAGGA TCGCTTCCCAAAACCCCCGCCATTGGCCCCCAGTTGCCGGGCCTCGGCCCCACAGTGCCCAAGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:5719809..5720150 26863196 MeRIP-seq:(Medium) rs953392115 Functional Loss SNV dbSNP153 33..33 33 - - - 81238 RMVar_ID_81238 Human_SNP_ID_656821318 m1A Human chr19 + 5720102 5720102 5720102 CCGCCGCAGCACCCAGCACCGCGCCGCTCCCCACAGTCGCACGTAGCCAGTGCTCGCCGCCATAG CCGCCGCAGCACCCAGCACCGCGCCGCTCCCCGCAGTCGCACGTAGCCAGTGCTCGCCGCCATAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr19:5719681..5720228;chr19:5719801..5720150 26863196 MeRIP-seq:(Medium) rs1216107912 Functional Loss SNV dbSNP153 33..33 33 - - - 81239 RMVar_ID_81239 Human_SNP_ID_656841203 m1A Human chr19 - 5783127 5783127 5783127 AGGAGCAGCCGCCCCACCCGGGGCCCCCTGCCACCAACACCCCGGCCCCCATTCTGTCTGGCAAG AGGAGCAGCCGCCCCACCCGGGGCCCCCTGCCTCCAACACCCCGGCCCCCATTCTGTCTGGCAAG T A PRR22 Ensembl:ENSG00000212123 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5783042..5783170 26863196 MeRIP-seq:(Medium) rs1165466144 Functional Loss SNV dbSNP153 33..33 33 - - - 81240 RMVar_ID_81240 Human_SNP_ID_656841204 m1A Human chr19 - 5783127 5783127 5783127 AGGAGCAGCCGCCCCACCCGGGGCCCCCTGCCACCAACACCCCGGCCCCCATTCTGTCTGGCAAG AGGAGCAGCCGCCCCACCCGGGGCCCCCTGCCGCCAACACCCCGGCCCCCATTCTGTCTGGCAAG T C PRR22 Ensembl:ENSG00000212123 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5783042..5783170 26863196 MeRIP-seq:(Medium) rs1165466144 Functional Loss SNV dbSNP153 33..33 33 - - - 81241 RMVar_ID_81241 Human_SNP_ID_656842344 m1A Human chr19 + 5785435 5785435 5785435 TGCCTTCTGGCTGGCCATCAGCGTCTCCAGGTAGTCGCGGCCCAGGTAGTAGGGCGGCCGCTCGT TGCCTTCTGGCTGGCCATCAGCGTCTCCAGGTGGTCGCGGCCCAGGTAGTAGGGCGGCCGCTCGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5785280..5785621 32194978 MeRIP-seq:(Medium) rs1352609243 Functional Loss SNV dbSNP153 33..33 33 - - - 81242 RMVar_ID_81242 Human_SNP_ID_656842959 m1A Human chr19 + 5786908 5786908 5786908 GGCAGAGAGTGAGACGCAGAGAGGAAGAGACCAAGAGAGCCAGGCTGAGAGAGACAGAGAGAGAC GGCAGAGAGTGAGACGCAGAGAGGAAGAGACCGAGAGAGCCAGGCTGAGAGAGACAGAGAGAGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5786872..5786937 26863196 MeRIP-seq:(Medium) rs773577236 Functional Loss SNV dbSNP153 33..33 33 - - - 81243 RMVar_ID_81243 Human_SNP_ID_656843148 m1A Human chr19 + 5787202 5787202 5787202 ACCTACAGGACGGTGGTGGGAGGTGGTGGGAGATGGTGGGAGGTGGTGGGAGACGGTGGGAGGTG ACCTACAGGACGGTGGTGGGAGGTGGTGGGAGGTGGTGGGAGGTGGTGGGAGACGGTGGGAGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5787173..5787257 26863196 MeRIP-seq:(Medium) rs796405103 Functional Loss SNV dbSNP153 33..33 33 - - - 81244 RMVar_ID_81244 Human_SNP_ID_656844149 m1A Human chr19 - 5789337 5789337 5789337 CGAGGGCACGGCAGCCGAGGGCGCTCCCAGGCAGGAAAACTGTGGTGCCCAGCAGGTCCCCGCAG CGAGGGCACGGCAGCCGAGGGCGCTCCCAGGCCGGAAAACTGTGGTGCCCAGCAGGTCCCCGCAG T G DUS3L Ensembl:ENSG00000141994 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5789289..5789358 26863196 MeRIP-seq:(Medium) rs747413829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2056664 RMVar_hsa_circ_191758,RMVar_hsa_circ_375896 81245 RMVar_ID_81245 Human_SNP_ID_656844564 m1A Human chr19 + 5790239 5790239 5790239 CGGATCCGCTTAGCCTCAGGCTCAGCCAGCTCATTGCCAGCAGGGTCTCCTACCTCGGTTTCCCG CGGATCCGCTTAGCCTCAGGCTCAGCCAGCTCTTTGCCAGCAGGGTCTCCTACCTCGGTTTCCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5790051..5790834 26863196 MeRIP-seq:(Medium) rs773678024 Functional Loss SNV dbSNP153 33..33 33 - - - 81246 RMVar_ID_81246 Human_SNP_ID_656844938 m1A Human chr19 + 5791113 5791113 5791113 CGGCTCCCGAGTCGCCACCACCACCATTCTCTAGAGGAGCCTCCGCCGTTCCCTCCGCCATCGGC CGGCTCCCGAGTCGCCACCACCACCATTCTCTGGAGGAGCCTCCGCCGTTCCCTCCGCCATCGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5790998..5791194 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81247 RMVar_ID_81247 Human_SNP_ID_656844941 m1A Human chr19 + 5791115 5791115 5791115 GCTCCCGAGTCGCCACCACCACCATTCTCTAGAGGAGCCTCCGCCGTTCCCTCCGCCATCGGCGC GCTCCCGAGTCGCCACCACCACCATTCTCTAGTGGAGCCTCCGCCGTTCCCTCCGCCATCGGCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5790847..5791200 26863196 MeRIP-seq:(Medium) rs367868424 Functional Loss SNV dbSNP153 33..33 33 - - - 81248 RMVar_ID_81248 Human_SNP_ID_656849662 m1A Human chr19 + 5805213 5805213 5805213 GCGCCCCGCGCCCTCTGAGCCGCCGGCCGTCCAGGGCACCCACCCCCAGCCCCAGCCCCCGCCGG GCGCCCCGCGCCCTCTGAGCCGCCGGCCGTCCGGGGCACCCACCCCCAGCCCCAGCCCCCGCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5805119..5805229 26863196 MeRIP-seq:(Medium) rs1245879469 Functional Loss SNV dbSNP153 33..33 33 - - - 81249 RMVar_ID_81249 Human_SNP_ID_656856114 m1A Human chr19 - 5827864 5827864 5827864 CGCAGCCCGCAAGGCCGCGCCCCCAACCGCGCACGCGCGCGCCGCCGCCGGGGCCCCGCCCGACG CGCAGCCCGCAAGGCCGCGCCCCCAACCGCGCGCGCGCGCGCCGCCGCCGGGGCCCCGCCCGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5827816..5827924 26863196 MeRIP-seq:(Medium) rs1187563674 Functional Loss SNV dbSNP153 33..33 33 - - - 81250 RMVar_ID_81250 Human_SNP_ID_656876469 m1A Human chr19 + 5896304 5896304 5896304 AGGGCCACAGTAGGTGCTTAAGCAGCAGCAGCAGCTGTCGCTATGACTGAAATGGCTGGTGTTCA AGGGCCACAGTAGGTGCTTAAGCAGCAGCAGCGGCTGTCGCTATGACTGAAATGGCTGGTGTTCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5896300..5896451 32194978 MeRIP-seq:(Medium) rs1010397798 Functional Loss SNV dbSNP153 33..33 33 - - - 81251 RMVar_ID_81251 Human_SNP_ID_656876572 m1A Human chr19 - 5896518 5896518 5896518 CACCACCTGCATCAGCGCCCATGTCCGCGAGAAGCCCGACGACCCCCTGAACTACTTCCTCGGTG CACCACCTGCATCAGCGCCCATGTCCGCGAGACGCCCGACGACCCCCTGAACTACTTCCTCGGTG T G AC024592.3,NDUFA11 Ensembl:ENSG00000267740,Ensembl:ENSG00000174886 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5896416..5896533 26863196 MeRIP-seq:(Medium) rs1486094875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240664,Human_RBP_ID_528471,Human_RBP_ID_4559103,Human_RBP_ID_9328501,Human_RBP_ID_18191888,Human_RBP_ID_18741410,Human_RBP_ID_23810122,Human_RBP_ID_26815079,Human_RBP_ID_27279485 Human_Splice_Rec_1943350,Human_Splice_Rec_1943351,Human_Splice_Rec_1943359,Human_Splice_Rec_1943364,Human_Splice_Rec_1943365,Human_Splice_Rec_1943370,Human_Splice_Rec_1943371,Human_Splice_Rec_1943376,Human_Splice_Rec_1943380,Human_Splice_Rec_1943381,Human_Splice_Rec_1943388,Human_Splice_Rec_1943389,Human_Splice_Rec_1943391,Human_Splice_Rec_1943398,Human_Splice_Rec_1943399 Human_miRNA_ID_2580000 RMVar_hsa_circ_123750,RMVar_hsa_circ_266807,RMVar_hsa_circ_191762,RMVar_hsa_circ_96891,RMVar_hsa_circ_191761 81252 RMVar_ID_81252 Human_SNP_ID_656876753 m1A Human chr19 - 5896953 5896953 5896953 CTGCCTACAGAGTCACACTCAATCCTCCGGGCACCTTCCTTGAAGGAGTGGCTAAGGTTGGACAA CTGCCTACAGAGTCACACTCAATCCTCCGGGCGCCTTCCTTGAAGGAGTGGCTAAGGTTGGACAA T C AC024592.3,NDUFA11 Ensembl:ENSG00000267740,Ensembl:ENSG00000174886 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:5896451..5903787 32194978 MeRIP-seq:(Medium) rs776094197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528480,Human_RBP_ID_1018967,Human_RBP_ID_1573772,Human_RBP_ID_1893317,Human_RBP_ID_3578453,Human_RBP_ID_4559104,Human_RBP_ID_17271224,Human_RBP_ID_17656650,Human_RBP_ID_17933217,Human_RBP_ID_18741417,Human_RBP_ID_22449160,Human_RBP_ID_23810126,Human_RBP_ID_26815082 Human_Splice_Rec_1943348,Human_Splice_Rec_1943349,Human_Splice_Rec_1943356,Human_Splice_Rec_1943357,Human_Splice_Rec_1943362,Human_Splice_Rec_1943363,Human_Splice_Rec_1943368,Human_Splice_Rec_1943369,Human_Splice_Rec_1943374,Human_Splice_Rec_1943375,Human_Splice_Rec_1943378,Human_Splice_Rec_1943379,Human_Splice_Rec_1943386,Human_Splice_Rec_1943387,Human_Splice_Rec_1943396,Human_Splice_Rec_1943397 Human_miRNA_ID_2144067,Human_miRNA_ID_2145596,Human_miRNA_ID_2688095,Human_miRNA_ID_2709148,Human_miRNA_ID_2903183 RMVar_hsa_circ_18660,RMVar_hsa_circ_123750,RMVar_hsa_circ_191762,RMVar_hsa_circ_96891,RMVar_hsa_circ_191761 81253 RMVar_ID_81253 Human_SNP_ID_656878705 m1A Human chr19 + 5903723 5903723 5903723 AAAAACCTTCGGCGCCATAGCCCGCAATCTCGATCCCGCACCACGGACCCCGCCAGCTCGGGAAG AAAAACCTTCGGCGCCATAGCCCGCAATCTCGTTCCCGCACCACGGACCCCGCCAGCTCGGGAAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5903295..5903787 26863196 MeRIP-seq:(Medium) rs1269017784 Functional Loss SNV dbSNP153 33..33 33 - - - 81254 RMVar_ID_81254 Human_SNP_ID_656884813 m1A Human chr19 + 5923153 5923153 5923153 GGCCCAGCCCTTGCGGTTGGACCCCCAGGTGCATGGAAGACCCAGGGCCACCGAGGAGGGGCCGG GGCCCAGCCCTTGCGGTTGGACCCCCAGGTGCGTGGAAGACCCAGGGCCACCGAGGAGGGGCCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:5923127..5923212 26863410 MeRIP-seq:(Medium) rs1236673903 Functional Loss SNV dbSNP153 33..33 33 - - - 81255 RMVar_ID_81255 Human_SNP_ID_656885406 m1A Human chr19 - 5924892 5924892 5924892 TTGCACATCTTCTCTTCAGTTTAGAGAACTCAACCAATAGTGCCGACGCCTCCAGCAACAAATTT TTGCACATCTTCTCTTCAGTTTAGAGAACTCAGCCAATAGTGCCGACGCCTCCAGCAACAAATTT T C RANBP3 Ensembl:ENSG00000031823 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:5924843..5924944 32194978 MeRIP-seq:(Medium) rs776072699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13528388 Human_Splice_Rec_1943462,Human_Splice_Rec_1943463,Human_Splice_Rec_1943494,Human_Splice_Rec_1943495,Human_Splice_Rec_1943526,Human_Splice_Rec_1943527,Human_Splice_Rec_1943548,Human_Splice_Rec_1943549,Human_Splice_Rec_1943578,Human_Splice_Rec_1943579,Human_Splice_Rec_1943608,Human_Splice_Rec_1943609,Human_Splice_Rec_1943641,Human_Splice_Rec_1943660,Human_Splice_Rec_1943661,Human_Splice_Rec_1943666,Human_Splice_Rec_1943667,Human_Splice_Rec_1943688 RMVar_hsa_circ_1788,RMVar_hsa_circ_191765,RMVar_hsa_circ_124907,RMVar_hsa_circ_333342,RMVar_hsa_circ_30678,RMVar_hsa_circ_54791,RMVar_hsa_circ_191767,RMVar_hsa_circ_8860,RMVar_hsa_circ_303604,RMVar_hsa_circ_365543,RMVar_hsa_circ_191768,RMVar_hsa_circ_27543 81256 RMVar_ID_81256 Human_SNP_ID_656885649 m1A Human chr19 - 5925681 5925681 5925681 GCCGACATGGAGAATGCTGGACACCCCAGCGCAGACACGCCAACCGCAACGAACTATTTCCTCCA GCCGACATGGAGAATGCTGGACACCCCAGCGCGGACACGCCAACCGCAACGAACTATTTCCTCCA T C RANBP3 Ensembl:ENSG00000031823 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:5925626..5925725 26863196 MeRIP-seq:(Medium) rs201521234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1893414,Human_RBP_ID_18741643,Human_RBP_ID_26337190 Human_Splice_Rec_1943460,Human_Splice_Rec_1943461,Human_Splice_Rec_1943492,Human_Splice_Rec_1943493,Human_Splice_Rec_1943524,Human_Splice_Rec_1943525,Human_Splice_Rec_1943546,Human_Splice_Rec_1943547,Human_Splice_Rec_1943576,Human_Splice_Rec_1943577,Human_Splice_Rec_1943606,Human_Splice_Rec_1943607,Human_Splice_Rec_1943640,Human_Splice_Rec_1943658,Human_Splice_Rec_1943659,Human_Splice_Rec_1943665,Human_Splice_Rec_1943686,Human_Splice_Rec_1943687,Human_Splice_Rec_1943698,Human_Splice_Rec_1943700 Human_miRNA_ID_1009288,Human_miRNA_ID_2141509 RMVar_hsa_circ_1788,RMVar_hsa_circ_191765,RMVar_hsa_circ_124907,RMVar_hsa_circ_333342,RMVar_hsa_circ_30678,RMVar_hsa_circ_54791,RMVar_hsa_circ_191767,RMVar_hsa_circ_8860,RMVar_hsa_circ_303604,RMVar_hsa_circ_365543,RMVar_hsa_circ_191768,RMVar_hsa_circ_27543,RMVar_hsa_circ_191770,RMVar_hsa_circ_369672 81257 RMVar_ID_81257 Human_SNP_ID_656890133 m1A Human chr19 - 5941707 5941707 5941707 TTTTCTCCTCCTCTTCTCATCATTTTCTGTAGATTCTGACAGAGAAGATGGAAATTACTGCCCTC TTTTCTCCTCCTCTTCTCATCATTTTCTGTAGGTTCTGACAGAGAAGATGGAAATTACTGCCCTC T C RANBP3 Ensembl:ENSG00000031823 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5941676..5941761 26863196 MeRIP-seq:(Medium) rs1259901225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369820,Human_RBP_ID_9381785,Human_RBP_ID_13529056,Human_RBP_ID_18996231,Human_RBP_ID_22661860 Human_Splice_Rec_1943450,Human_Splice_Rec_1943451,Human_Splice_Rec_1943482,Human_Splice_Rec_1943483,Human_Splice_Rec_1943512,Human_Splice_Rec_1943513,Human_Splice_Rec_1943566,Human_Splice_Rec_1943567,Human_Splice_Rec_1943596,Human_Splice_Rec_1943597,Human_Splice_Rec_1943650,Human_Splice_Rec_1943651,Human_Splice_Rec_1943676,Human_Splice_Rec_1943677,Human_Splice_Rec_1943706,Human_Splice_Rec_1943707,Human_Splice_Rec_1943720,Human_Splice_Rec_1943721,Human_Splice_Rec_1943734,Human_Splice_Rec_1943735,Human_Splice_Rec_1943746,Human_Splice_Rec_1943747,Human_Splice_Rec_1943762,Human_Splice_Rec_1943763,Human_Splice_Rec_1943774,Human_Splice_Rec_1943775,Human_Splice_Rec_1943786,Human_Splice_Rec_1943787,Human_Splice_Rec_1943800,Human_Splice_Rec_1943801,Human_Splice_Rec_1943812,Human_Splice_Rec_1943813,Human_Splice_Rec_1943826,Human_Splice_Rec_1943827,Human_Splice_Rec_1943836,Human_Splice_Rec_1943837,Human_Splice_Rec_1943846,Human_Splice_Rec_1943847,Human_Splice_Rec_1943858,Human_Splice_Rec_1943859,Human_Splice_Rec_1943868,Human_Splice_Rec_1943878 RMVar_hsa_circ_191765,RMVar_hsa_circ_124907,RMVar_hsa_circ_333342,RMVar_hsa_circ_191767,RMVar_hsa_circ_33748,RMVar_hsa_circ_76953,RMVar_hsa_circ_191771,RMVar_hsa_circ_191776,RMVar_hsa_circ_314250,RMVar_hsa_circ_191772,RMVar_hsa_circ_110655,RMVar_hsa_circ_324263,RMVar_hsa_circ_338408,RMVar_hsa_circ_119749,RMVar_hsa_circ_294515,RMVar_hsa_circ_7222,RMVar_hsa_circ_191777,RMVar_hsa_circ_191774,RMVar_hsa_circ_191775,RMVar_hsa_circ_191773 81258 RMVar_ID_81258 Human_SNP_ID_656890924 m1A Human chr19 + 5944672 5944667 5944673 TAGGCTGGCTTTGGCCTCCAAATGCTCTGTGCAGGTCACTGTCTGAGGCCAGCAGCCTCTGCACA TAGGCTGGCTTTGGCCTCCAAATGCTCT______GTCACTGTCTGAGGCCAGCAGCCTCTGCACA TGTGCAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5944668..5945147 26863196 MeRIP-seq:(Medium) rs1432963084 Functional Loss DEL dbSNP153 29..34 33 - - - 81259 RMVar_ID_81259 Human_SNP_ID_656890927 m1A Human chr19 + 5944672 5944672 5944672 TAGGCTGGCTTTGGCCTCCAAATGCTCTGTGCAGGTCACTGTCTGAGGCCAGCAGCCTCTGCACA TAGGCTGGCTTTGGCCTCCAAATGCTCTGTGCTGGTCACTGTCTGAGGCCAGCAGCCTCTGCACA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5944668..5945147 26863196 MeRIP-seq:(Medium) rs985474898 Functional Loss SNV dbSNP153 33..33 33 - - - 81260 RMVar_ID_81260 Human_SNP_ID_656892421 m1A Human chr19 - 5950248 5950244 5950249 GAGACACGGGAGCCGCGGGAAGGAGTCCAGCCAGGAGGCACTTGACCCACAGTGCACTGGGAGTA GAGACACGGGAGCCGCGGGAAGGAGTCCAGC_____GGCACTTGACCCACAGTGCACTGGGAGTA CTCCTG C RANBP3 Ensembl:ENSG00000031823 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:5950245..5950380 26863196 MeRIP-seq:(Medium) rs1194496020 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_769828,Human_RBP_ID_8195973,Human_RBP_ID_26785176 RMVar_hsa_circ_191772,RMVar_hsa_circ_110655,RMVar_hsa_circ_338408,RMVar_hsa_circ_119749,RMVar_hsa_circ_294515,RMVar_hsa_circ_7222,RMVar_hsa_circ_191774,RMVar_hsa_circ_191775,RMVar_hsa_circ_191773 81261 RMVar_ID_81261 Human_SNP_ID_656954029 m1A Human chr19 - 6196325 6196325 6196325 AGTGAGAGAGTTCCCAAGGGAGCTGGAAGAAGAGTGGTGAGATGGAGGAGGTAAATAAGGTGTGG AGTGAGAGAGTTCCCAAGGGAGCTGGAAGAAGCGTGGTGAGATGGAGGAGGTAAATAAGGTGTGG T G RFX2 Ensembl:ENSG00000087903 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6196275..6196451 26863196 MeRIP-seq:(Medium) rs1418120423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23810615 81262 RMVar_ID_81262 Human_SNP_ID_656959394 m1A Human chr19 + 6212974 6212974 6212974 GGCAGTGCTGCGGGCAGGCGAGACGGGAGAGGAGGGCAGGCGAGGCCTGGCTGCAGCCTCCCAGG GGCAGTGCTGCGGGCAGGCGAGACGGGAGAGGGGGGCAGGCGAGGCCTGGCTGCAGCCTCCCAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6212924..6213043 26863196 MeRIP-seq:(Medium) rs1174818048 Functional Loss SNV dbSNP153 33..33 33 - - - 81263 RMVar_ID_81263 Human_SNP_ID_656959846 m1A Human chr19 - 6214024 6214024 6214024 CCCCGTGTGTCGGTTCAGGTTGAGCTTCAGCGACAGCGAGAGTGACAACAGCGCCGACTCCTCCC CCCCGTGTGTCGGTTCAGGTTGAGCTTCAGCGGCAGCGAGAGTGACAACAGCGCCGACTCCTCCC T C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6213926..6214126 26863196 MeRIP-seq:(Medium) rs1368624048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53945,Human_RBP_ID_3954277,Human_RBP_ID_5371133,Human_RBP_ID_9346661,Human_RBP_ID_18741748,Human_RBP_ID_22812804 Human_Splice_Rec_1944330,Human_Splice_Rec_1944331,Human_Splice_Rec_1944342,Human_Splice_Rec_1944343 RMVar_hsa_circ_103247,RMVar_hsa_circ_88013,RMVar_hsa_circ_191790,RMVar_hsa_circ_121318,RMVar_hsa_circ_377538,RMVar_hsa_circ_124471,RMVar_hsa_circ_191791,RMVar_hsa_circ_191792,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793 81264 RMVar_ID_81264 Human_SNP_ID_656962423 m1A Human chr19 - 6222326 6222323 6222326 CTCGCCAAAGCCCAGCGCCAAGAAGCAGAAGAAGAGCAGCTCGAAGGGGTCCCGGAGTGCTCCAG CTCGCCAAAGCCCAGCGCCAAGAAGCAGAAGA___GCAGCTCGAAGGGGTCCCGGAGTGCTCCAG CTCT C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6222093..6230758 26863196 MeRIP-seq:(Medium) rs755830979 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_103247,RMVar_hsa_circ_88013,RMVar_hsa_circ_191790,RMVar_hsa_circ_121318,RMVar_hsa_circ_124471,RMVar_hsa_circ_191791,RMVar_hsa_circ_191792,RMVar_hsa_circ_12618,RMVar_hsa_circ_19782,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_374734,RMVar_hsa_circ_191796,RMVar_hsa_circ_17517,RMVar_hsa_circ_373252,RMVar_hsa_circ_191797 81265 RMVar_ID_81265 Human_SNP_ID_656962485 m1A Human chr19 + 6222432 6222432 6222432 TGGGGGTGGGGGTGGGGGCCCACCCTTGGGGGACGTGCTTTCCAGCTTGGTCTCTTTCAGGGCCA TGGGGGTGGGGGTGGGGGCCCACCCTTGGGGGGCGTGCTTTCCAGCTTGGTCTCTTTCAGGGCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972533,GSM1972534 HEK293T,ALKBH3 KO;HEPG2 cell line,total RNA Untreated chr19:6222287..6222433;chr19:6222308..6222437 26863410,26863196 MeRIP-seq:(Medium) rs758219842 Functional Loss SNV dbSNP153 33..33 33 - - - 81266 RMVar_ID_81266 Human_SNP_ID_656962509 m1A Human chr19 - 6222496 6222496 6222496 GAGGGCCGGCTGCCCAAGGAGGAGAAGGCGCCACCGCCCAAGGCTGCCTTCAAGGAACCCAAGAT GAGGGCCGGCTGCCCAAGGAGGAGAAGGCGCCTCCGCCCAAGGCTGCCTTCAAGGAACCCAAGAT T A MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6222447..6222700 26863196 MeRIP-seq:(Medium) rs1422713829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908371,Human_RBP_ID_27814979 RMVar_hsa_circ_103247,RMVar_hsa_circ_88013,RMVar_hsa_circ_191790,RMVar_hsa_circ_121318,RMVar_hsa_circ_124471,RMVar_hsa_circ_191791,RMVar_hsa_circ_191792,RMVar_hsa_circ_12618,RMVar_hsa_circ_19782,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_374734,RMVar_hsa_circ_191796,RMVar_hsa_circ_17517,RMVar_hsa_circ_373252,RMVar_hsa_circ_191797 81267 RMVar_ID_81267 Human_SNP_ID_656962510 m1A Human chr19 - 6222496 6222496 6222496 GAGGGCCGGCTGCCCAAGGAGGAGAAGGCGCCACCGCCCAAGGCTGCCTTCAAGGAACCCAAGAT GAGGGCCGGCTGCCCAAGGAGGAGAAGGCGCCGCCGCCCAAGGCTGCCTTCAAGGAACCCAAGAT T C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6222447..6222700 26863196 MeRIP-seq:(Medium) rs1422713829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908371,Human_RBP_ID_27814979 RMVar_hsa_circ_103247,RMVar_hsa_circ_88013,RMVar_hsa_circ_191790,RMVar_hsa_circ_121318,RMVar_hsa_circ_124471,RMVar_hsa_circ_191791,RMVar_hsa_circ_191792,RMVar_hsa_circ_12618,RMVar_hsa_circ_19782,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_374734,RMVar_hsa_circ_191796,RMVar_hsa_circ_17517,RMVar_hsa_circ_373252,RMVar_hsa_circ_191797 81268 RMVar_ID_81268 Human_SNP_ID_656963773 m1A Human chr19 + 6227026 6227026 6227026 GTTTGGTCTTCTTGGGGTCAGAGAAGGCAGAGAGTGGAATTGTGGGTAACATGGGGTAGTCGGGA GTTTGGTCTTCTTGGGGTCAGAGAAGGCAGAGTGTGGAATTGTGGGTAACATGGGGTAGTCGGGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:6226976..6227125;chr19:6226976..6227050 26863196 MeRIP-seq:(Medium) rs1032330894 Functional Loss SNV dbSNP153 33..33 33 - - - 81269 RMVar_ID_81269 Human_SNP_ID_656964498 m1A Human chr19 + 6229525 6229525 6229525 CACCCGCATACCCCACACGTCATACATGCCACATACACACCTGACACATTCACATACTCCCCATA CACCCGCATACCCCACACGTCATACATGCCACGTACACACCTGACACATTCACATACTCCCCATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6229523..6229677 26863196 MeRIP-seq:(Medium) rs968873468 Functional Loss SNV dbSNP153 33..33 33 - - - 81270 RMVar_ID_81270 Human_SNP_ID_656964531 m1A Human chr19 + 6229613 6229612 6229614 TGACACACCACACACTTCCCGCAAGTGACACGACACACACGCCATGCACACACCATACATGACAC TGACACACCACACACTTCCCGCAAGTGACACG__ACACACGCCATGCACACACCATACATGACAC GAC G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:6229597..6229865 26863196 MeRIP-seq:(Medium) rs1347449863 Functional Loss DEL dbSNP153 33..34 33 - - - 81271 RMVar_ID_81271 Human_SNP_ID_656964834 m1A Human chr19 - 6230623 6230623 6230623 CGCCCGTGAACCACCTGCGCTGCGAGAAGCTCACCTTCAACAACCCCACCACGGAGTTCCGGTAC CGCCCGTGAACCACCTGCGCTGCGAGAAGCTCGCCTTCAACAACCCCACCACGGAGTTCCGGTAC T C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6230495..6230725 26863196 MeRIP-seq:(Medium) rs1470610088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1019058,Human_RBP_ID_6792810,Human_RBP_ID_9292978,Human_RBP_ID_17271270,Human_RBP_ID_17386178,Human_RBP_ID_17696596,Human_RBP_ID_17933443,Human_RBP_ID_26997177 Human_Splice_Rec_1944320,Human_Splice_Rec_1944321 RMVar_hsa_circ_103247,RMVar_hsa_circ_124471,RMVar_hsa_circ_191792,RMVar_hsa_circ_106203,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_17517,RMVar_hsa_circ_373252,RMVar_hsa_circ_116392,RMVar_hsa_circ_191799,RMVar_hsa_circ_191797,RMVar_hsa_circ_320665,RMVar_hsa_circ_291229,RMVar_hsa_circ_110627,RMVar_hsa_circ_191800,RMVar_hsa_circ_191802,RMVar_hsa_circ_191803,RMVar_hsa_circ_191801,RMVar_hsa_circ_191804 81272 RMVar_ID_81272 Human_SNP_ID_656966173 m1A Human chr19 - 6235589 6235589 6235589 GGTGCACAGCTGTGGCCAGGAGTGTGGAGAGGAGAGGACCCAGTTCCGAGCCCCAGGGTGCCCTG GGTGCACAGCTGTGGCCAGGAGTGTGGAGAGGGGAGGACCCAGTTCCGAGCCCCAGGGTGCCCTG T C MLLT1 Ensembl:ENSG00000130382 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6235587..6235733 26863196 MeRIP-seq:(Medium) rs996181532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3587819 RMVar_hsa_circ_103247,RMVar_hsa_circ_124471,RMVar_hsa_circ_191792,RMVar_hsa_circ_106203,RMVar_hsa_circ_191794,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_373252,RMVar_hsa_circ_191797,RMVar_hsa_circ_320665,RMVar_hsa_circ_291229,RMVar_hsa_circ_110627,RMVar_hsa_circ_191802,RMVar_hsa_circ_191803,RMVar_hsa_circ_191801,RMVar_hsa_circ_191804 81273 RMVar_ID_81273 Human_SNP_ID_656975733 m1A Human chr19 - 6270638 6270638 6270638 GTTTGTCCGCGGCCCCGAGCAATGTGACATCCAGCACTTCGTGGAGAAGGTGGTCTTCTGGCTGC GTTTGTCCGCGGCCCCGAGCAATGTGACATCCGGCACTTCGTGGAGAAGGTGGTCTTCTGGCTGC T C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6270542..6270804 26863196 MeRIP-seq:(Medium) rs770902024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574136,Human_RBP_ID_1893494,Human_RBP_ID_5144980,Human_RBP_ID_22504006 Human_Splice_Rec_1944317 RMVar_hsa_circ_103247,RMVar_hsa_circ_124471,RMVar_hsa_circ_191792,RMVar_hsa_circ_191794,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_373252,RMVar_hsa_circ_191797,RMVar_hsa_circ_320665,RMVar_hsa_circ_291229,RMVar_hsa_circ_110627,RMVar_hsa_circ_191802,RMVar_hsa_circ_191803,RMVar_hsa_circ_87079,RMVar_hsa_circ_191804,RMVar_hsa_circ_282830,RMVar_hsa_circ_330457,RMVar_hsa_circ_191805,RMVar_hsa_circ_191806 81274 RMVar_ID_81274 Human_SNP_ID_656978328 m1A Human chr19 - 6279876 6279873 6279877 GCGGCGGCGGCGGCGGCGGCGGCGCTTGACAGACAATGAGGGCGGCGGGGCGGCGTTGAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCGCTTGACA____ATGAGGGCGGCGGGGCGGCGTTGAGCGGCG TTGTC T MLLT1 Ensembl:ENSG00000130382 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:6279752..6279936 26863196 MeRIP-seq:(Medium) rs1463974511 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_4557970,Human_RBP_ID_18442144 RMVar_hsa_circ_110627,RMVar_hsa_circ_191803,RMVar_hsa_circ_87079,RMVar_hsa_circ_191805 81275 RMVar_ID_81275 Human_SNP_ID_656978350 m1A Human chr19 - 6279912 6279912 6279912 CCGCGGGGCTGGCGGGCGAGCGGGCGGCCGGGATCGGCGGCGGCGGCGGCGGCGGCGGCGCTTGA CCGCGGGGCTGGCGGGCGAGCGGGCGGCCGGGGTCGGCGGCGGCGGCGGCGGCGGCGGCGCTTGA T C MLLT1 Ensembl:ENSG00000130382 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:6270545..6280006;chr19:6279603..6279950;chr19:6279751..6279975;chr19:6279736..6280000;chr19:6279719..6280004;chr19:6279751..6279947 26863196 MeRIP-seq:(Medium) rs1456940605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138074,Human_RBP_ID_4557970,Human_RBP_ID_9328527,Human_RBP_ID_18421242,Human_RBP_ID_18461805 RMVar_hsa_circ_110627,RMVar_hsa_circ_191803,RMVar_hsa_circ_87079,RMVar_hsa_circ_191805 81276 RMVar_ID_81276 Human_SNP_ID_657001654 m1A Human chr19 - 6361594 6361594 6361594 GGTACCTGCATGACGCCACCCGGGCCCCCCCTACCAATATTCCGGGCCACATCCCTCCGCACGCC GGTACCTGCATGACGCCACCCGGGCCCCCCCTTCCAATATTCCGGGCCACATCCCTCCGCACGCC T A AC011491.3 Ensembl:ENSG00000269802 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6361500..6362027 26863196 MeRIP-seq:(Medium) rs556537852 Functional Loss SNV dbSNP153 33..33 33 - - - 81277 RMVar_ID_81277 Human_SNP_ID_657002080 m1A Human chr19 + 6362496 6362496 6362496 AGCCTTGTTATCGCACAGCTCCTCTTCCTGCAATCCGAGAGCAACAAGAAGCCCATCCACATGTA AGCCTTGTTATCGCACAGCTCCTCTTCCTGCAGTCCGAGAGCAACAAGAAGCCCATCCACATGTA A G CLPP Ensembl:ENSG00000125656 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr19:6362409..6362550;chr19:6362422..6364650 26863196,32194978 MeRIP-seq:(Medium) rs150689749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528770,Human_RBP_ID_1374597,Human_RBP_ID_1574142,Human_RBP_ID_1893495,Human_RBP_ID_17933454,Human_RBP_ID_26815100 Human_Splice_Rec_1944370,Human_Splice_Rec_1944371,Human_Splice_Rec_1944379,Human_Splice_Rec_1944388,Human_Splice_Rec_1944389,Human_Splice_Rec_1944394,Human_Splice_Rec_1944395,Human_Splice_Rec_1944402,Human_Splice_Rec_1944403,Human_Splice_Rec_1944410,Human_Splice_Rec_1944411 Human_miRNA_ID_1768161 RMVar_hsa_circ_124177,RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_315727,RMVar_hsa_circ_191809 81278 RMVar_ID_81278 Human_SNP_ID_657002684 m1A Human chr19 + 6364517 6364517 6364517 ACACGATGCAGTACATCCTCAACCCGATCTGCACCTGGTGCGTGGGCCAGGCCGCCAGCATGGGC ACACGATGCAGTACATCCTCAACCCGATCTGCCCCTGGTGCGTGGGCCAGGCCGCCAGCATGGGC A C CLPP Ensembl:ENSG00000125656 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6364501..6364525 26863196 MeRIP-seq:(Medium) rs398123033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528773,Human_RBP_ID_4553226,Human_RBP_ID_17670211,Human_RBP_ID_26815103 Human_Splice_Rec_1944372,Human_Splice_Rec_1944380,Human_Splice_Rec_1944390,Human_Splice_Rec_1944396,Human_Splice_Rec_1944404 Clinvar_Rec_381 RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_315727,RMVar_hsa_circ_85054,RMVar_hsa_circ_354732,RMVar_hsa_circ_313370,RMVar_hsa_circ_191810,RMVar_hsa_circ_191811 81279 RMVar_ID_81279 Human_SNP_ID_657002685 m1A Human chr19 + 6364517 6364517 6364517 ACACGATGCAGTACATCCTCAACCCGATCTGCACCTGGTGCGTGGGCCAGGCCGCCAGCATGGGC ACACGATGCAGTACATCCTCAACCCGATCTGCGCCTGGTGCGTGGGCCAGGCCGCCAGCATGGGC A G CLPP Ensembl:ENSG00000125656 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6364501..6364525 26863196 MeRIP-seq:(Medium) rs398123033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528773,Human_RBP_ID_4553226,Human_RBP_ID_17670211,Human_RBP_ID_26815103 Human_Splice_Rec_1944372,Human_Splice_Rec_1944380,Human_Splice_Rec_1944390,Human_Splice_Rec_1944396,Human_Splice_Rec_1944404 Clinvar_Rec_381 RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_315727,RMVar_hsa_circ_85054,RMVar_hsa_circ_354732,RMVar_hsa_circ_313370,RMVar_hsa_circ_191810,RMVar_hsa_circ_191811 81280 RMVar_ID_81280 Human_SNP_ID_657002724 m1A Human chr19 - 6364606 6364606 6364606 CGGGCGCCTCCTGAGGGCTGGTGGATCATGATACGGGAGTTGGGGAGCGAGTGGCGCATGCCTGG CGGGCGCCTCCTGAGGGCTGGTGGATCATGATGCGGGAGTTGGGGAGCGAGTGGCGCATGCCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:6364405..6364696;chr19:6364413..6364681 26863196 MeRIP-seq:(Medium) rs1410714248 Functional Loss SNV dbSNP153 33..33 33 - - - 81281 RMVar_ID_81281 Human_SNP_ID_657003205 m1A Human chr19 - 6366188 6366188 6366188 GTATCGGCGTCAGCCCCTCACAGGGAGGCTGGAGGTGGCACTCAGGAGCTTCCCTGGGCTTTGGG GTATCGGCGTCAGCCCCTCACAGGGAGGCTGGGGGTGGCACTCAGGAGCTTCCCTGGGCTTTGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:6366185..6366325 26863410 MeRIP-seq:(Medium) rs1021222832 Functional Loss SNV dbSNP153 33..33 33 - - - 81282 RMVar_ID_81282 Human_SNP_ID_657005273 m1A Human chr19 - 6372837 6372837 6372837 AGCTGGGCCCTGGCAGCGTCCGCAGCGCCAGCAGCCCAGTCCCGGCCATAATCCCGGAGCGGGGT AGCTGGGCCCTGGCAGCGTCCGCAGCGCCAGCGGCCCAGTCCCGGCCATAATCCCGGAGCGGGGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:6372801..6373025 26863196 MeRIP-seq:(Medium) rs1223828672 Functional Loss SNV dbSNP153 33..33 33 - - - 81283 RMVar_ID_81283 Human_SNP_ID_657005280 m1A Human chr19 - 6372846 6372846 6372846 CTCGCACCCAGCTGGGCCCTGGCAGCGTCCGCAGCGCCAGCAGCCCAGTCCCGGCCATAATCCCG CTCGCACCCAGCTGGGCCCTGGCAGCGTCCGCTGCGCCAGCAGCCCAGTCCCGGCCATAATCCCG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6372776..6374325 26863196 MeRIP-seq:(Medium) rs752519508 Functional Loss SNV dbSNP153 33..33 33 - - - 81284 RMVar_ID_81284 Human_SNP_ID_657005281 m1A Human chr19 - 6372846 6372846 6372846 CTCGCACCCAGCTGGGCCCTGGCAGCGTCCGCAGCGCCAGCAGCCCAGTCCCGGCCATAATCCCG CTCGCACCCAGCTGGGCCCTGGCAGCGTCCGCCGCGCCAGCAGCCCAGTCCCGGCCATAATCCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6372776..6374325 26863196 MeRIP-seq:(Medium) rs752519508 Functional Loss SNV dbSNP153 33..33 33 - - - 81285 RMVar_ID_81285 Human_SNP_ID_657005285 m1A Human chr19 + 6372851 6372851 6372851 TTATGGCCGGGACTGGGCTGCTGGCGCTGCGGACGCTGCCAGGGCCCAGCTGGGTGCGAGGCTCG TTATGGCCGGGACTGGGCTGCTGGCGCTGCGGGCGCTGCCAGGGCCCAGCTGGGTGCGAGGCTCG A G ALKBH7 Ensembl:ENSG00000125652 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr19:6372801..6374357;chr19:6372801..6372975;chr19:6372801..6374302 26863196 MeRIP-seq:(Medium) rs1222635055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4553259,Human_RBP_ID_5320099,Human_RBP_ID_9328529,Human_RBP_ID_22448229,Human_RBP_ID_23810741 RMVar_hsa_circ_105662,RMVar_hsa_circ_191814 81286 RMVar_ID_81286 Human_SNP_ID_657005290 m1A Human chr19 - 6372855 6372855 6372855 GGCCCGAGCCTCGCACCCAGCTGGGCCCTGGCAGCGTCCGCAGCGCCAGCAGCCCAGTCCCGGCC GGCCCGAGCCTCGCACCCAGCTGGGCCCTGGCGGCGTCCGCAGCGCCAGCAGCCCAGTCCCGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6372776..6374325 26863196 MeRIP-seq:(Medium) rs1413871451 Functional Loss SNV dbSNP153 33..33 33 - - - 81287 RMVar_ID_81287 Human_SNP_ID_657005992 m1A Human chr19 + 6374532 6374520 6374532 GTCTCCCAGCGTTATGCGGCTGGTGCACACCCAGGAGCCGGGGGAGTGGCTGGAACTCTTGCTGG GTCTCCCAGCGTTATGCGGCT____________GGAGCCGGGGGAGTGGCTGGAACTCTTGCTGG TGGTGCACACCCA T ALKBH7 Ensembl:ENSG00000125652 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:6374496..6374815 26863410 MeRIP-seq:(Medium) rs751339323 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5469315,Human_RBP_ID_18192835,Human_RBP_ID_22446354,Human_RBP_ID_22504009,Human_RBP_ID_26815109 Human_Splice_Rec_1944420,Human_Splice_Rec_1944421,Human_Splice_Rec_1944426,Human_Splice_Rec_1944427,Human_Splice_Rec_1944432,Human_Splice_Rec_1944433 Human_miRNA_ID_2041352,Human_miRNA_ID_3020335 RMVar_hsa_circ_105662,RMVar_hsa_circ_191814,RMVar_hsa_circ_376729 81288 RMVar_ID_81288 Human_SNP_ID_657005999 m1A Human chr19 + 6374532 6374532 6374532 GTCTCCCAGCGTTATGCGGCTGGTGCACACCCAGGAGCCGGGGGAGTGGCTGGAACTCTTGCTGG GTCTCCCAGCGTTATGCGGCTGGTGCACACCCTGGAGCCGGGGGAGTGGCTGGAACTCTTGCTGG A T ALKBH7 Ensembl:ENSG00000125652 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:6374496..6374815 26863410 MeRIP-seq:(Medium) rs1286466509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5469315,Human_RBP_ID_18192835,Human_RBP_ID_22446354,Human_RBP_ID_22504009,Human_RBP_ID_26815109 Human_Splice_Rec_1944420,Human_Splice_Rec_1944421,Human_Splice_Rec_1944426,Human_Splice_Rec_1944427,Human_Splice_Rec_1944432,Human_Splice_Rec_1944433 Human_miRNA_ID_2041352,Human_miRNA_ID_3020335 RMVar_hsa_circ_105662,RMVar_hsa_circ_191814,RMVar_hsa_circ_376729 81289 RMVar_ID_81289 Human_SNP_ID_657006027 m1A Human chr19 + 6374588 6374588 6374588 TCTTGCTGGAGCCGGGCTCCCTCTACATCCTTAGGTACCTCCATCCAGGCAGCACCCACCCCTCC TCTTGCTGGAGCCGGGCTCCCTCTACATCCTTCGGTACCTCCATCCAGGCAGCACCCACCCCTCC A C ALKBH7 Ensembl:ENSG00000125652 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6374452..6374612 26863196 MeRIP-seq:(Medium) rs769282339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5469316,Human_RBP_ID_17933469,Human_RBP_ID_18192835,Human_RBP_ID_22446354 Human_Splice_Rec_1944421,Human_Splice_Rec_1944427,Human_Splice_Rec_1944433 RMVar_hsa_circ_105662,RMVar_hsa_circ_191814,RMVar_hsa_circ_376729 81290 RMVar_ID_81290 Human_SNP_ID_657006028 m1A Human chr19 + 6374588 6374588 6374588 TCTTGCTGGAGCCGGGCTCCCTCTACATCCTTAGGTACCTCCATCCAGGCAGCACCCACCCCTCC TCTTGCTGGAGCCGGGCTCCCTCTACATCCTTGGGTACCTCCATCCAGGCAGCACCCACCCCTCC A G ALKBH7 Ensembl:ENSG00000125652 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6374452..6374612 26863196 MeRIP-seq:(Medium) rs769282339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5469316,Human_RBP_ID_17933469,Human_RBP_ID_18192835,Human_RBP_ID_22446354 Human_Splice_Rec_1944421,Human_Splice_Rec_1944427,Human_Splice_Rec_1944433 RMVar_hsa_circ_105662,RMVar_hsa_circ_191814,RMVar_hsa_circ_376729 81291 RMVar_ID_81291 Human_SNP_ID_657007858 m1A Human chr19 - 6380001 6379994 6380001 ATTGTCCTCCTCCTCCTGGCTCGGCCTCCCTCACACTGACCAAGGGCCTGTGCTGCCCACTGGGT ATTGTCCTCCTCCTCCTGGCTCGGCCTCCCTC_______CCAAGGGCCTGTGCTGCCCACTGGGT GTCAGTGT G GTF2F1 Ensembl:ENSG00000125651 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:6379951..6380155 26863196 MeRIP-seq:(Medium) rs1381818242 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_55202,Human_RBP_ID_6792907,Human_RBP_ID_8197484,Human_RBP_ID_17502063,Human_RBP_ID_18191903,Human_RBP_ID_18741795,Human_RBP_ID_20427375,Human_RBP_ID_22069018,Human_RBP_ID_22240742,Human_RBP_ID_22812818,Human_RBP_ID_22976978,Human_RBP_ID_26475231,Human_RBP_ID_26997210,Human_RBP_ID_27472486 81292 RMVar_ID_81292 Human_SNP_ID_657008093 m1A Human chr19 + 6380648 6380648 6380648 ACTTCCCAGACAGGCTCTGGGGTCCCGTGTCCAGCCGCAACCGCTTGGCTGCAGGCATCTCGCTC ACTTCCCAGACAGGCTCTGGGGTCCCGTGTCCGGCCGCAACCGCTTGGCTGCAGGCATCTCGCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6380626..6380650 26863196 MeRIP-seq:(Medium) rs1391925622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191818 81293 RMVar_ID_81293 Human_SNP_ID_657008479 m1A Human chr19 - 6381415 6381413 6381416 GAGTGAGGAGGAGAAGCCGCCTGAGGAGGACAAGGAGGAGGAGGAGGAGAAGAAGGCACCCACCC GAGTGAGGAGGAGAAGCCGCCTGAGGAGGAC___GAGGAGGAGGAGGAGAAGAAGGCACCCACCC CCTT C GTF2F1 Ensembl:ENSG00000125651 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6381351..6381450 26863196 MeRIP-seq:(Medium) rs758707853 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8176,Human_RBP_ID_53523,Human_RBP_ID_203266,Human_RBP_ID_771154,Human_RBP_ID_825682,Human_RBP_ID_913737,Human_RBP_ID_5526788,Human_RBP_ID_6792915,Human_RBP_ID_9381790,Human_RBP_ID_18544502,Human_RBP_ID_19088906,Human_RBP_ID_21979649,Human_RBP_ID_22977388,Human_RBP_ID_24545411,Human_RBP_ID_26335380,Human_RBP_ID_27814984 Human_Splice_Rec_1944452,Human_Splice_Rec_1944453,Human_Splice_Rec_1944470,Human_Splice_Rec_1944471,Human_Splice_Rec_1944482,Human_Splice_Rec_1944483,Human_Splice_Rec_1944491,Human_Splice_Rec_1944516 RMVar_hsa_circ_77893,RMVar_hsa_circ_191815,RMVar_hsa_circ_191816,RMVar_hsa_circ_191820,RMVar_hsa_circ_191819,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 81294 RMVar_ID_81294 Human_SNP_ID_657009250 m1A Human chr19 + 6383402 6383399 6383402 TGGATGCGCAGCTCGCTCGCCTTCCTGCGGCCACGTTTCTCCTTCTCCTCCTCATCCTCGTCCTG TGGATGCGCAGCTCGCTCGCCTTCCTGCGG___CGTTTCTCCTTCTCCTCCTCATCCTCGTCCTG GCCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:6383351..6383425 26863196 MeRIP-seq:(Medium) rs757784641 Functional Loss DEL dbSNP153 31..33 33 - - - 81295 RMVar_ID_81295 Human_SNP_ID_657011101 m1A Human chr19 + 6389601 6389601 6389601 CGCGCCCGATTCGGGCATCTCCTCCTCTTGGTAGATTTTCTTGTTGCTCAAGTCCCGCTCCAGCC CGCGCCCGATTCGGGCATCTCCTCCTCTTGGTGGATTTTCTTGTTGCTCAAGTCCCGCTCCAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6389551..6389625 26863196 MeRIP-seq:(Medium) rs1486791504 Functional Loss SNV dbSNP153 33..33 33 - - - 81296 RMVar_ID_81296 Human_SNP_ID_657012362 m1A Human chr19 + 6393266 6393265 6393266 TCGCGATGGCAACCTTCTTAGCGACTGTGGCCACCTCAGTGCGCAGTCACTTATGCTCCTCGGCG TCGCGATGGCAACCTTCTTAGCGACTGTGGCC_CCTCAGTGCGCAGTCACTTATGCTCCTCGGCG CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6393217..6393353 26863196 MeRIP-seq:(Medium) rs561279930 Functional Loss DEL dbSNP153 33..33 33 - - - 81297 RMVar_ID_81297 Human_SNP_ID_657018759 m1A Human chr19 + 6413442 6413440 6413442 ACAATTTTTTTTGTTGTTCTCATTTTGTTTTCAGTTTCAATCTCCTCTTGAACAGATGAAAAGAC ACAATTTTTTTTGTTGTTCTCATTTTGTTTT__GTTTCAATCTCCTCTTGAACAGATGAAAAGAC TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6413392..6413612 26863196 MeRIP-seq:(Medium) rs1232965080 Functional Loss DEL dbSNP153 32..33 33 - - - 81298 RMVar_ID_81298 Human_SNP_ID_657019138 m1A Human chr19 - 6414211 6414211 6414211 CAGGTTTGGGAGGGGGCTTCCTGGCCCCCCCCACGGTGTTCCAGCCCCTCCTCTCTTCCGCCCCC CAGGTTTGGGAGGGGGCTTCCTGGCCCCCCCCCCGGTGTTCCAGCCCCTCCTCTCTTCCGCCCCC T G KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:6414168..6414567 26863196 MeRIP-seq:(Medium) rs1394929605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528866,Human_RBP_ID_4553443,Human_RBP_ID_5116613,Human_RBP_ID_5130970,Human_RBP_ID_6793014,Human_RBP_ID_17271294,Human_RBP_ID_27279920 81299 RMVar_ID_81299 Human_SNP_ID_657019194 m1A Human chr19 - 6414278 6414276 6414278 CTTCAGCGAGTCCCGCGAGCACCTGGCTAGACAGTTAACAAGCACGTCCTTCCAGCCTGAGCCAG CTTCAGCGAGTCCCGCGAGCACCTGGCTAGAC__TTAACAAGCACGTCCTTCCAGCCTGAGCCAG ACT A KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:6414187..6414281 26863410 MeRIP-seq:(Medium) rs1198518383 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_528867,Human_RBP_ID_1574205,Human_RBP_ID_1893532,Human_RBP_ID_3578730,Human_RBP_ID_6793015,Human_RBP_ID_8199369,Human_RBP_ID_8496418,Human_RBP_ID_13531483,Human_RBP_ID_17271294,Human_RBP_ID_18741821,Human_RBP_ID_20427445,Human_RBP_ID_22979937,Human_RBP_ID_23810798,Human_RBP_ID_25438070,Human_RBP_ID_26475247 81300 RMVar_ID_81300 Human_SNP_ID_657019241 m1A Human chr19 + 6414350 6414350 6414350 GCTCCCTGATGGAGAAGGAGGGACAGAGCAGGAAGAGAGGAGAGGGGCCGCGGAGGGCGGAGGCG GCTCCCTGATGGAGAAGGAGGGACAGAGCAGGGAGAGAGGAGAGGGGCCGCGGAGGGCGGAGGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:6414176..6414880 26863196 MeRIP-seq:(Medium) rs181050702 Functional Loss SNV dbSNP153 33..33 33 - - - 81301 RMVar_ID_81301 Human_SNP_ID_657019457 m1A Human chr19 - 6414788 6414788 6414788 CAGCGCGGACGGTGGGCACCGGCCCGGCCGCCACCACCTCGCTCACAATCTGGCCACTTGGGAAG CAGCGCGGACGGTGGGCACCGGCCCGGCCGCCGCCACCTCGCTCACAATCTGGCCACTTGGGAAG T C KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6414749..6414890 26863196 MeRIP-seq:(Medium) rs1243516164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528891,Human_RBP_ID_1893540,Human_RBP_ID_6793046,Human_RBP_ID_8496430,Human_RBP_ID_17933537,Human_RBP_ID_18741832,Human_RBP_ID_26470838,Human_RBP_ID_27472525 81302 RMVar_ID_81302 Human_SNP_ID_657019613 m1A Human chr19 - 6415150 6415150 6415150 GGCGGCCCCCAGCCGCCGCCCACGCAGCAGGGACAGCAGCAGGCAAGTGGGAATTGCCACCCTCC GGCGGCCCCCAGCCGCCGCCCACGCAGCAGGGGCAGCAGCAGGCAAGTGGGAATTGCCACCCTCC T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:6415101..6415150 26863196 MeRIP-seq:(Medium) rs1374370141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54965,Human_RBP_ID_528903,Human_RBP_ID_4553495,Human_RBP_ID_6793056,Human_RBP_ID_13531534,Human_RBP_ID_27279937 RMVar_hsa_circ_48353,RMVar_hsa_circ_64113 81303 RMVar_ID_81303 Human_SNP_ID_657019753 m1A Human chr19 - 6415445 6415437 6415446 CTGTCTCGGCGCCCGCACAGGCCAGCAGCCCCAGCAGCCCGGAGCACCCCCACAGCAGGACTACA CTGTCTCGGCGCCCGCACAGGCCAGCAGCCC_________GGAGCACCCCCACAGCAGGACTACA CGGGCTGCTG C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6414726..6415702 26863196 MeRIP-seq:(Medium) rs945742526 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_773425,Human_RBP_ID_5375401 Human_Splice_Rec_1944574,Human_Splice_Rec_1944575,Human_Splice_Rec_1944578,Human_Splice_Rec_1944579,Human_Splice_Rec_1944614,Human_Splice_Rec_1944615,Human_Splice_Rec_1944617,Human_Splice_Rec_1944628,Human_Splice_Rec_1944629,Human_Splice_Rec_1944632,Human_Splice_Rec_1944633,Human_Splice_Rec_1944636,Human_Splice_Rec_1944637,Human_Splice_Rec_1944639 RMVar_hsa_circ_48353,RMVar_hsa_circ_64113 81304 RMVar_ID_81304 Human_SNP_ID_657019871 m1A Human chr19 + 6415650 6415638 6415650 GTGGGGCCGCAGGGGCCGGTGCGGGGCCGGGGACGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG GTGGGGCCGCAGGGGCCGGTG____________CGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG GCGGGGCCGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6415526..6415661 26863196 MeRIP-seq:(Medium) rs1453482140 Functional Loss DEL dbSNP153 22..33 33 - - - 81305 RMVar_ID_81305 Human_SNP_ID_657019878 m1A Human chr19 + 6415650 6415644 6415650 GTGGGGCCGCAGGGGCCGGTGCGGGGCCGGGGACGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG GTGGGGCCGCAGGGGCCGGTGCGGGGC______CGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG CCGGGGA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6415526..6415661 26863196 MeRIP-seq:(Medium) rs1323723905 Functional Loss DEL dbSNP153 28..33 33 - - - 81306 RMVar_ID_81306 Human_SNP_ID_657019886 m1A Human chr19 + 6415650 6415650 6415650 GTGGGGCCGCAGGGGCCGGTGCGGGGCCGGGGACGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG GTGGGGCCGCAGGGGCCGGTGCGGGGCCGGGGCCGGGGCCCGGGGGCTGCTGGTAGTAGTGTGAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6415526..6415661 26863196 MeRIP-seq:(Medium) rs1473236555 Functional Loss SNV dbSNP153 33..33 33 - - - 81307 RMVar_ID_81307 Human_SNP_ID_657020308 m1A Human chr19 - 6416497 6416497 6416497 GATTGACCACGCCAAGCAGCTTATCGAGGAAAAGATCGAGGTGGGTTGGGGCGGGCTCTGGGGAT GATTGACCACGCCAAGCAGCTTATCGAGGAAAGGATCGAGGTGGGTTGGGGCGGGCTCTGGGGAT T C KHSRP,MIR3940 Ensembl:ENSG00000088247,Ensembl:ENSG00000284159 Protein coding,miRNA CDS,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1163363357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528914,Human_RBP_ID_769524,Human_RBP_ID_1893552,Human_RBP_ID_3578750,Human_RBP_ID_5585953,Human_RBP_ID_6793082,Human_RBP_ID_8496441,Human_RBP_ID_9090425,Human_RBP_ID_17502093,Human_RBP_ID_18442156,Human_RBP_ID_18996245,Human_RBP_ID_22240797,Human_RBP_ID_22504024,Human_RBP_ID_22524560,Human_RBP_ID_22812859,Human_RBP_ID_22979940,Human_RBP_ID_25438099,Human_RBP_ID_26997280,Human_RBP_ID_27279949 Human_Splice_Rec_1944567,Human_Splice_Rec_1944607,Human_Splice_Rec_1944621 RMVar_hsa_circ_28642,RMVar_hsa_circ_64113 81308 RMVar_ID_81308 Human_SNP_ID_657020433 m1A Human chr19 + 6416802 6416802 6416802 GGGATGGAGAAGGTCATCTCCCCGCCAGGGGGACCCCAATTGCCTTGGCCTCTTCCTCGGCCTCG GGGATGGAGAAGGTCATCTCCCCGCCAGGGGGGCCCCAATTGCCTTGGCCTCTTCCTCGGCCTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6416664..6416857 26863196 MeRIP-seq:(Medium) rs895033381 Functional Loss SNV dbSNP153 33..33 33 - - - 81309 RMVar_ID_81309 Human_SNP_ID_657020860 m1A Human chr19 + 6417729 6417729 6417729 TGGGGGTGCACTGGCCAGGGGCAGGGTGGGCCAGGCCCTGACCTTGCTTGAACTGTATCCGCACG TGGGGGTGCACTGGCCAGGGGCAGGGTGGGCCGGGCCCTGACCTTGCTTGAACTGTATCCGCACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6417726..6417800 26863196 MeRIP-seq:(Medium) rs1568342917 Functional Loss SNV dbSNP153 33..33 33 - - - 81310 RMVar_ID_81310 Human_SNP_ID_657020870 m1A Human chr19 - 6417783 6417783 6417783 CGTGGTCATTGGCCGGAGTGGAGAGATGATCAAGAAGATCCAGAATGATGCTGGCGTGCGGATAC CGTGGTCATTGGCCGGAGTGGAGAGATGATCAGGAAGATCCAGAATGATGCTGGCGTGCGGATAC T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:6414651..6420150 32194978 MeRIP-seq:(Medium) rs1452370293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528920,Human_RBP_ID_1019124,Human_RBP_ID_1574242,Human_RBP_ID_1893558,Human_RBP_ID_3578754,Human_RBP_ID_3956104,Human_RBP_ID_4574478,Human_RBP_ID_5194307,Human_RBP_ID_6793104,Human_RBP_ID_8496450,Human_RBP_ID_8838367,Human_RBP_ID_9258945,Human_RBP_ID_9380230,Human_RBP_ID_13531571,Human_RBP_ID_17933566,Human_RBP_ID_18741862,Human_RBP_ID_22448233,Human_RBP_ID_22812866,Human_RBP_ID_22979941,Human_RBP_ID_23810811 Human_Splice_Rec_1944560,Human_Splice_Rec_1944561,Human_Splice_Rec_1944600,Human_Splice_Rec_1944601,Human_Splice_Rec_1944656,Human_Splice_Rec_1944674 Human_miRNA_ID_2442329,Human_miRNA_ID_2565715 RMVar_hsa_circ_16929,RMVar_hsa_circ_127710,RMVar_hsa_circ_111872,RMVar_hsa_circ_191822,RMVar_hsa_circ_114390,RMVar_hsa_circ_191823,RMVar_hsa_circ_191824 81311 RMVar_ID_81311 Human_SNP_ID_657020996 m1A Human chr19 - 6418035 6418035 6418035 ATGGTGATGGACATCCTCCGGGAACGTGACCAAGGCGGCTTTGGGGACCGGAATGAGTACGGATC ATGGTGATGGACATCCTCCGGGAACGTGACCAGGGCGGCTTTGGGGACCGGAATGAGTACGGATC T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr19:6417943..6418089;chr19:6417976..6418100 26863196 MeRIP-seq:(Medium) rs750620888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528922,Human_RBP_ID_1893561,Human_RBP_ID_3578756,Human_RBP_ID_3954293,Human_RBP_ID_4574484,Human_RBP_ID_6793110,Human_RBP_ID_8838369,Human_RBP_ID_9380232,Human_RBP_ID_13531583,Human_RBP_ID_17933567,Human_RBP_ID_23810814,Human_RBP_ID_26334793,Human_RBP_ID_27815926 Human_Splice_Rec_1944558,Human_Splice_Rec_1944559,Human_Splice_Rec_1944598,Human_Splice_Rec_1944599,Human_Splice_Rec_1944654,Human_Splice_Rec_1944655,Human_Splice_Rec_1944672,Human_Splice_Rec_1944673,Human_Splice_Rec_1944692 Human_miRNA_ID_2669007,Human_miRNA_ID_3010969 RMVar_hsa_circ_16929,RMVar_hsa_circ_127710,RMVar_hsa_circ_111872,RMVar_hsa_circ_191822,RMVar_hsa_circ_114390,RMVar_hsa_circ_191823,RMVar_hsa_circ_191824 81312 RMVar_ID_81312 Human_SNP_ID_657021217 m1A Human chr19 + 6418573 6418573 6418573 GATCCGTCCTGAATTAAGATCATCTTCACTCCAGCGCGTTCCTTTACAAGCAAGGTTAACCGTTA GATCCGTCCTGAATTAAGATCATCTTCACTCCGGCGCGTTCCTTTACAAGCAAGGTTAACCGTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:6418526..6418600;chr19:6418526..6418910 26863196 MeRIP-seq:(Medium) rs374062788 Functional Loss SNV dbSNP153 33..33 33 - - - 81313 RMVar_ID_81313 Human_SNP_ID_657021222 m1A Human chr19 - 6418579 6418579 6418579 CAGCACTAACGGTTAACCTTGCTTGTAAAGGAACGCGCTGGAGTGAAGATGATCTTAATTCAGGA CAGCACTAACGGTTAACCTTGCTTGTAAAGGAGCGCGCTGGAGTGAAGATGATCTTAATTCAGGA T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6418501..6418600 26863196 MeRIP-seq:(Medium) rs1387357397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574252,Human_RBP_ID_1893564,Human_RBP_ID_6793116,Human_RBP_ID_8838374,Human_RBP_ID_9294114,Human_RBP_ID_13531590,Human_RBP_ID_25438115,Human_RBP_ID_26335393 Human_Splice_Rec_1944556,Human_Splice_Rec_1944557,Human_Splice_Rec_1944596,Human_Splice_Rec_1944597,Human_Splice_Rec_1944652,Human_Splice_Rec_1944653,Human_Splice_Rec_1944670,Human_Splice_Rec_1944671,Human_Splice_Rec_1944690,Human_Splice_Rec_1944691 RMVar_hsa_circ_16929,RMVar_hsa_circ_127710,RMVar_hsa_circ_111872,RMVar_hsa_circ_191822,RMVar_hsa_circ_114390,RMVar_hsa_circ_79928,RMVar_hsa_circ_191823,RMVar_hsa_circ_191824,RMVar_hsa_circ_104572,RMVar_hsa_circ_339759,RMVar_hsa_circ_191826,RMVar_hsa_circ_47098,RMVar_hsa_circ_191825 81314 RMVar_ID_81314 Human_SNP_ID_657021292 m1A Human chr19 + 6418714 6418714 6418714 TGCCCAGGTGCTGCCCTCACCTGCAGCTGCTTAATGGTCTCCCCGCCCTTGCCAATGACCAGGCC TGCCCAGGTGCTGCCCTCACCTGCAGCTGCTTGATGGTCTCCCCGCCCTTGCCAATGACCAGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6418447..6418915 26863196 MeRIP-seq:(Medium) rs1568343606 Functional Loss SNV dbSNP153 33..33 33 - - - 81315 RMVar_ID_81315 Human_SNP_ID_657021508 m1A Human chr19 - 6419247 6419247 6419247 CTCTATCTCCTCTTTTCAGACAGCGGTGGCCTACCCGAGCGCAGTGTGTCCTTGACAGGAGCCCC CTCTATCTCCTCTTTTCAGACAGCGGTGGCCTGCCCGAGCGCAGTGTGTCCTTGACAGGAGCCCC T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6419201..6419275 26863196 MeRIP-seq:(Medium) rs756393005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239314,Human_RBP_ID_528927,Human_RBP_ID_912436,Human_RBP_ID_1019135,Human_RBP_ID_1574264,Human_RBP_ID_1893567,Human_RBP_ID_3578762,Human_RBP_ID_4553572,Human_RBP_ID_6793124,Human_RBP_ID_8496461,Human_RBP_ID_8838381,Human_RBP_ID_9292996,Human_RBP_ID_17933574,Human_RBP_ID_18741877,Human_RBP_ID_22448234,Human_RBP_ID_22504031,Human_RBP_ID_22661890 Human_Splice_Rec_1944552,Human_Splice_Rec_1944553,Human_Splice_Rec_1944592,Human_Splice_Rec_1944593,Human_Splice_Rec_1944648,Human_Splice_Rec_1944649,Human_Splice_Rec_1944666,Human_Splice_Rec_1944667,Human_Splice_Rec_1944686,Human_Splice_Rec_1944687,Human_Splice_Rec_1944702,Human_Splice_Rec_1944703 Human_miRNA_ID_1959667 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_127710,RMVar_hsa_circ_111872,RMVar_hsa_circ_191822,RMVar_hsa_circ_114390,RMVar_hsa_circ_79928,RMVar_hsa_circ_191823,RMVar_hsa_circ_191824,RMVar_hsa_circ_339759,RMVar_hsa_circ_191826,RMVar_hsa_circ_47098 81316 RMVar_ID_81316 Human_SNP_ID_657021512 m1A Human chr19 + 6419253 6419253 6419253 CCTGTCAAGGACACACTGCGCTCGGGTAGGCCACCGCTGTCTGAAAAGAGGAGATAGAGTCAGTG CCTGTCAAGGACACACTGCGCTCGGGTAGGCCGCCGCTGTCTGAAAAGAGGAGATAGAGTCAGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6419174..6419302 26863196 MeRIP-seq:(Medium) rs1291612236 Functional Loss SNV dbSNP153 33..33 33 - - - 81317 RMVar_ID_81317 Human_SNP_ID_657021515 m1A Human chr19 - 6419258 6419258 6419258 GAGGGCACTGACTCTATCTCCTCTTTTCAGACAGCGGTGGCCTACCCGAGCGCAGTGTGTCCTTG GAGGGCACTGACTCTATCTCCTCTTTTCAGACGGCGGTGGCCTACCCGAGCGCAGTGTGTCCTTG T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:6419201..6419275 31548705,26863196 m1A-IP-seq:(High) rs1411628906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912436,Human_RBP_ID_1574264,Human_RBP_ID_1893567,Human_RBP_ID_4553573,Human_RBP_ID_6793124,Human_RBP_ID_22448234,Human_RBP_ID_22661890 Human_Splice_Rec_1944552,Human_Splice_Rec_1944553,Human_Splice_Rec_1944592,Human_Splice_Rec_1944593,Human_Splice_Rec_1944648,Human_Splice_Rec_1944649,Human_Splice_Rec_1944666,Human_Splice_Rec_1944667,Human_Splice_Rec_1944686,Human_Splice_Rec_1944687,Human_Splice_Rec_1944702,Human_Splice_Rec_1944703 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_127710,RMVar_hsa_circ_111872,RMVar_hsa_circ_191822,RMVar_hsa_circ_114390,RMVar_hsa_circ_79928,RMVar_hsa_circ_191823,RMVar_hsa_circ_191824,RMVar_hsa_circ_339759,RMVar_hsa_circ_191826,RMVar_hsa_circ_47098 81318 RMVar_ID_81318 Human_SNP_ID_657021915 m1A Human chr19 + 6420404 6420403 6420404 TTCCTCCTGGGGAAGAGTGGGCCTCCCCACCCAAGGTGACCCACACTCACTCAGGCCCACCATGC TTCCTCCTGGGGAAGAGTGGGCCTCCCCACCC_AGGTGACCCACACTCACTCAGGCCCACCATGC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:6420401..6420475;chr19:6420401..6420450 26863196,32194978,32194978 MeRIP-seq:(Medium) rs772747376 Functional Loss DEL dbSNP153 33..33 33 - - - 81319 RMVar_ID_81319 Human_SNP_ID_657021916 m1A Human chr19 + 6420404 6420404 6420404 TTCCTCCTGGGGAAGAGTGGGCCTCCCCACCCAAGGTGACCCACACTCACTCAGGCCCACCATGC TTCCTCCTGGGGAAGAGTGGGCCTCCCCACCCCAGGTGACCCACACTCACTCAGGCCCACCATGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:6420401..6420475;chr19:6420401..6420450 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1177821091 Functional Loss SNV dbSNP153 33..33 33 - - - 81320 RMVar_ID_81320 Human_SNP_ID_657022188 m1A Human chr19 - 6421279 6421279 6421279 GTTCTCAACTTGGACCCATCCATCCTCCCCCAAGGTAAGCCATGGTGGGGCCCACACTGCTTTCT GTTCTCAACTTGGACCCATCCATCCTCCCCCACGGTAAGCCATGGTGGGGCCCACACTGCTTTCT T G KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:6421276..6421325 32194978 MeRIP-seq:(Medium) rs1442582441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574301,Human_RBP_ID_1893574,Human_RBP_ID_6793155,Human_RBP_ID_8496479,Human_RBP_ID_8838385,Human_RBP_ID_9346856,Human_RBP_ID_9380236,Human_RBP_ID_17271325,Human_RBP_ID_17386211,Human_RBP_ID_17502098,Human_RBP_ID_17933581,Human_RBP_ID_19088925,Human_RBP_ID_22504035,Human_RBP_ID_22664671,Human_RBP_ID_26655590 Human_Splice_Rec_1944546,Human_Splice_Rec_1944547,Human_Splice_Rec_1944586,Human_Splice_Rec_1944587,Human_Splice_Rec_1944642,Human_Splice_Rec_1944643,Human_Splice_Rec_1944662,Human_Splice_Rec_1944663,Human_Splice_Rec_1944680,Human_Splice_Rec_1944681,Human_Splice_Rec_1944696,Human_Splice_Rec_1944697 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_114390,RMVar_hsa_circ_191824,RMVar_hsa_circ_47098,RMVar_hsa_circ_23523,RMVar_hsa_circ_191827,RMVar_hsa_circ_97293 81321 RMVar_ID_81321 Human_SNP_ID_657022287 m1A Human chr19 - 6421571 6421571 6421571 AGGTTTTCAGGAGTCAGGAGCTGGAAGCACTGAGGAGGTGGCAGCTCTTTACAGAGGCCCCTGGT AGGTTTTCAGGAGTCAGGAGCTGGAAGCACTGGGGAGGTGGCAGCTCTTTACAGAGGCCCCTGGT T C KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6421569..6421634 26863196 MeRIP-seq:(Medium) rs1028551003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371169,Human_RBP_ID_13531725,Human_RBP_ID_17133014,Human_RBP_ID_19095708,Human_RBP_ID_22545501,Human_RBP_ID_22664672,Human_RBP_ID_22742391,Human_RBP_ID_23131927 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_23523,RMVar_hsa_circ_191827,RMVar_hsa_circ_97293 81322 RMVar_ID_81322 Human_SNP_ID_657022580 m1A Human chr19 - 6422431 6422431 6422431 TCTTCTGTGCTTACTACTTTATTCTAGATTGCAGCCAAAATTGGAGGCGATGCTGCCACGACAGT TCTTCTGTGCTTACTACTTTATTCTAGATTGCGGCCAAAATTGGAGGCGATGCTGCCACGACAGT T C KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6422326..6422450 26863196 MeRIP-seq:(Medium) rs1404485746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574313,Human_RBP_ID_8838992,Human_RBP_ID_17933584 Human_Splice_Rec_1944542,Human_Splice_Rec_1944543,Human_Splice_Rec_1944582,Human_Splice_Rec_1944583,Human_Splice_Rec_1944658,Human_Splice_Rec_1944659,Human_Splice_Rec_1944676,Human_Splice_Rec_1944677,Human_Splice_Rec_1944693,Human_Splice_Rec_1944705 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_23523,RMVar_hsa_circ_191827,RMVar_hsa_circ_97293 81323 RMVar_ID_81323 Human_SNP_ID_657022581 m1A Human chr19 - 6422431 6422431 6422431 TCTTCTGTGCTTACTACTTTATTCTAGATTGCAGCCAAAATTGGAGGCGATGCTGCCACGACAGT TCTTCTGTGCTTACTACTTTATTCTAGATTGCCGCCAAAATTGGAGGCGATGCTGCCACGACAGT T G KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6422326..6422450 26863196 MeRIP-seq:(Medium) rs1404485746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574313,Human_RBP_ID_8838992,Human_RBP_ID_17933584 Human_Splice_Rec_1944542,Human_Splice_Rec_1944543,Human_Splice_Rec_1944582,Human_Splice_Rec_1944583,Human_Splice_Rec_1944658,Human_Splice_Rec_1944659,Human_Splice_Rec_1944676,Human_Splice_Rec_1944677,Human_Splice_Rec_1944693,Human_Splice_Rec_1944705 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_23523,RMVar_hsa_circ_191827,RMVar_hsa_circ_97293 81324 RMVar_ID_81324 Human_SNP_ID_657023396 m1A Human chr19 + 6424612 6424612 6424612 CCCCGGTCCCCCGCGCCTGGCGGGCCCGGCGGAGGGCCTCCCCCGGCGCCTCCGGCTCCCCCGCC CCCCGGTCCCCCGCGCCTGGCGGGCCCGGCGGCGGGCCTCCCCCGGCGCCTCCGGCTCCCCCGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:6424406..6424825;chr19:6424576..6424750 26863196 MeRIP-seq:(Medium) rs1331360422 Functional Loss SNV dbSNP153 33..33 33 - - - 81325 RMVar_ID_81325 Human_SNP_ID_657023455 m1A Human chr19 + 6424744 6424743 6424744 GGCCGGGCCTGGCGCGGAGGCTGAAGCTGAGGAGGCGGCGGCGGCGGCGGCGGCTCAACGCGGGA GGCCGGGCCTGGCGCGGAGGCTGAAGCTGAGG_GGCGGCGGCGGCGGCGGCGGCTCAACGCGGGA GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:6424526..6424825;chr19:6424652..6424800 26863196 MeRIP-seq:(Medium) rs1448679309 Functional Loss DEL dbSNP153 33..33 33 - - - 81326 RMVar_ID_81326 Human_SNP_ID_657023473 m1A Human chr19 - 6424766 6424766 6424766 GCCGTGTGGAGCGAGGCCTTGTTCCCGCGTTGAGCCGCCGCCGCCGCCGCCGCCTCCTCAGCTTC GCCGTGTGGAGCGAGGCCTTGTTCCCGCGTTGGGCCGCCGCCGCCGCCGCCGCCTCCTCAGCTTC T C KHSRP Ensembl:ENSG00000088247 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:6424396..6424825;chr19:6424684..6424790;chr19:6424412..6424825;chr19:6424417..6424825 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1228628256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557977,Human_RBP_ID_9293000,Human_RBP_ID_9328534,Human_RBP_ID_18741904,Human_RBP_ID_22533103 RMVar_hsa_circ_191827,RMVar_hsa_circ_97293 81327 RMVar_ID_81327 Human_SNP_ID_657026238 m1A Human chr19 + 6431783 6431783 6431783 GTCTTTAAACTCGTCCAAAGACCCCATCCCCAATTCCCTGACCTCCAACCCCCACCTTGGCCCAG GTCTTTAAACTCGTCCAAAGACCCCATCCCCAGTTCCCTGACCTCCAACCCCCACCTTGGCCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6431754..6432056 26863196 MeRIP-seq:(Medium) rs940723715 Functional Loss SNV dbSNP153 33..33 33 - - - 81328 RMVar_ID_81328 Human_SNP_ID_657028852 m1A Human chr19 + 6440956 6440956 6440956 AGTGCCTTGGAATATCAGGATCTGCCTTCAAGAGATGAGGTTTCAACATTGAGGGACTGGGCAGA AGTGCCTTGGAATATCAGGATCTGCCTTCAAGGGATGAGGTTTCAACATTGAGGGACTGGGCAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:6440955..6441055 32194978 MeRIP-seq:(Medium) rs1385999886 Functional Loss SNV dbSNP153 33..33 33 - - - 81329 RMVar_ID_81329 Human_SNP_ID_657032456 m1A Human chr19 + 6454648 6454648 6454648 TGCCACTGCGCCGGCCACCAGCTGTTTCCACCACATGCCCGTCAGCTTCTCTTGCTTTGAGAACT TGCCACTGCGCCGGCCACCAGCTGTTTCCACCGCATGCCCGTCAGCTTCTCTTGCTTTGAGAACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6454598..6454705 26863196 MeRIP-seq:(Medium) rs748355158 Functional Loss SNV dbSNP153 33..33 33 - - - 81330 RMVar_ID_81330 Human_SNP_ID_657033359 m1A Human chr19 + 6457542 6457534 6457543 AAATTTTCTCAGCCTGCTCCAGCGAGATGGAAATGCCCAGAGCTCGGAAACTCTGTTGGATCTCA AAATTTTCTCAGCCTGCTCCAGCGA_________GCCCAGAGCTCGGAAACTCTGTTGGATCTCA AGATGGAAAT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:6456430..6457551 32194978 MeRIP-seq:(Medium) rs768402884 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_191836 81331 RMVar_ID_81331 Human_SNP_ID_657034006 m1A Human chr19 + 6459627 6459627 6459627 GCCGCCGCTCCGCGTCGCCCGGGCTCCCCCGCATGGCGCCCGCCCGGGGGGGAGGGGAGGCCCGG GCCGCCGCTCCGCGTCGCCCGGGCTCCCCCGCGTGGCGCCCGCCCGGGGGGGAGGGGAGGCCCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6459551..6459757 26863196 MeRIP-seq:(Medium) rs749507188 Functional Loss SNV dbSNP153 33..33 33 - - - 81332 RMVar_ID_81332 Human_SNP_ID_657034055 m1A Human chr19 - 6459696 6459696 6459696 CGGGAGCTGACCCTGCGGGGTCCCGGGGGGGGAGGGGGAGCCGCGAAGCCCCCACTGAGGCCGCC CGGGAGCTGACCCTGCGGGGTCCCGGGGGGGGGGGGGGAGCCGCGAAGCCCCCACTGAGGCCGCC T C SLC25A23 Ensembl:ENSG00000125648 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:6459526..6459775 26863410 MeRIP-seq:(Medium) rs537137506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557158,Human_RBP_ID_5239221 RMVar_hsa_circ_79615,RMVar_hsa_circ_191830,RMVar_hsa_circ_266857 81333 RMVar_ID_81333 Human_SNP_ID_657045044 m1A Human chr19 + 6495161 6495161 6495161 CCTCGAGGGGACAGGTGGGAAGCGATGGGAGCAGCCTAGGCCACCTCCTCCTCCGCCTCCTCCTC CCTCGAGGGGACAGGTGGGAAGCGATGGGAGCGGCCTAGGCCACCTCCTCCTCCGCCTCCTCCTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:6495110..6495260 32194978 MeRIP-seq:(Medium) rs150446118 Functional Loss SNV dbSNP153 33..33 33 - - - 81334 RMVar_ID_81334 Human_SNP_ID_657047337 m1A Human chr19 - 6502224 6502224 6502224 GCGCTCGTGCCACCGCCGCCGCGTCCACCCTCAGCGCCACCGCCATGCGGGAGATCGTGCACCTG GCGCTCGTGCCACCGCCGCCGCGTCCACCCTCGGCGCCACCGCCATGCGGGAGATCGTGCACCTG T C TUBB4A Ensembl:ENSG00000104833 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6502188..6502289 26863196 MeRIP-seq:(Medium) rs757740469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4553743 Human_Splice_Rec_1945167,Human_Splice_Rec_1945173,Human_Splice_Rec_1945175,Human_Splice_Rec_1945177,Human_Splice_Rec_1945181,Human_Splice_Rec_1945191,Human_Splice_Rec_1945201,Human_Splice_Rec_1945207,Human_Splice_Rec_1945215,Human_Splice_Rec_1945221,Human_Splice_Rec_1945227 81335 RMVar_ID_81335 Human_SNP_ID_657055455 m1A Human chr19 + 6531071 6531071 6531071 GGAATACGCCTCTGACGCTTCACTGGACCCCGAAGCCCCGTGGCCTCCCGCGCCCCGCGCTCGCG GGAATACGCCTCTGACGCTTCACTGGACCCCGGAGCCCCGTGGCCTCCCGCGCCCCGCGCTCGCG A G TNFSF9 Ensembl:ENSG00000125657 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:6531026..6531200 26863196 MeRIP-seq:(Medium) rs777954592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9328536 81336 RMVar_ID_81336 Human_SNP_ID_657055962 m1A Human chr19 - 6532318 6532317 6532319 GCACCCCCACACGAACACACACACACGAACACAAACACCCACACAAACACGAACACACACACACA GCACCCCCACACGAACACACACACACGAACA__AACACCCACACAAACACGAACACACACACACA TTG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6532270..6532550 26863196 MeRIP-seq:(Medium) rs1406776752 Functional Loss DEL dbSNP153 32..33 33 - - - 81337 RMVar_ID_81337 Human_SNP_ID_657056083 m1A Human chr19 - 6532543 6532539 6532543 AACACCCACATTAACACACAGACACACGAACAAACACGAACACACACACGAACGCAAACACAAAC AACACCCACATTAACACACAGACACACGAACA____CGAACACACACACGAACGCAAACACAAAC GTGTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:6532258..6532651 26863196 MeRIP-seq:(Medium) rs893807267 Functional Loss DEL dbSNP153 33..36 33 - - - 81338 RMVar_ID_81338 Human_SNP_ID_657056314 m1A Human chr19 + 6533258 6533258 6533258 TCCTCCTTACTCCCATTCTCTTCCCCATCCCCAGGCCCTCCTCCTGTCCCCTTCCCTCCCCCTAG TCCTCCTTACTCCCATTCTCTTCCCCATCCCCCGGCCCTCCTCCTGTCCCCTTCCCTCCCCCTAG A C TNFSF9 Ensembl:ENSG00000125657 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6533255..6533435 26863196 MeRIP-seq:(Medium) rs1157249654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191838,RMVar_hsa_circ_115897 81339 RMVar_ID_81339 Human_SNP_ID_657071168 m1A Human chr19 + 6586352 6586351 6586352 CCCCTTGTCCAGCTCTGGTCCATGCAGGAAGGAGCGGCCCAGTGCTGGGCCCCCCTGCCAGTATA CCCCTTGTCCAGCTCTGGTCCATGCAGGAAGG_GCGGCCCAGTGCTGGGCCCCCCTGCCAGTATA GA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:6585986..6586383 32194978 MeRIP-seq:(Medium) rs1568431262 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_382 81340 RMVar_ID_81340 Human_SNP_ID_657072041 m1A Human chr19 - 6589095 6589093 6589095 GAGAGAACGAGAGAGAGAGAGAGGAGAGAGAGAGCGAGCAGGTTTGTGTTTCTGGGCATCCACTA GAGAGAACGAGAGAGAGAGAGAGGAGAGAGAG__CGAGCAGGTTTGTGTTTCTGGGCATCCACTA GCT G CD70 Ensembl:ENSG00000125726 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6589092..6589377 26863196 MeRIP-seq:(Medium) rs1303753475 Functional Loss DEL dbSNP153 33..34 33 - - - 81341 RMVar_ID_81341 Human_SNP_ID_657072289 m1A Human chr19 - 6589854 6589845 6589854 AAAAAGAACAGAGAGAGGGACAGAGGGGACAGACGGGACAGGAGAAGAAGGGGAAAGAAAGAAAC AAAAAGAACAGAGAGAGGGACAGAGGGGACAG_________GAGAAGAAGGGGAAAGAAAGAAAC CCTGTCCCGT C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6589851..6590080 26863196 MeRIP-seq:(Medium) rs772253471 Functional Loss DEL dbSNP153 33..41 33 - - - 81342 RMVar_ID_81342 Human_SNP_ID_657072677 m1A Human chr19 + 6591001 6591001 6591001 GCCGCACCGAGCAGCCCGAACCCTCCTCCGGCATCGCCGCGGCGATCACCTCCGCTAGCGCAGGA GCCGCACCGAGCAGCCCGAACCCTCCTCCGGCGTCGCCGCGGCGATCACCTCCGCTAGCGCAGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6590951..6591150 26863196 MeRIP-seq:(Medium) rs1290546351 Functional Loss SNV dbSNP153 33..33 33 - - - 81343 RMVar_ID_81343 Human_SNP_ID_657072706 m1A Human chr19 + 6591062 6591062 6591062 AGGAGGGGCGATGGGGGCGCGGAGCGCTGCCGAGAAGGAAGGAAGGAAACTGCAGCCCCCTCCCG AGGAGGGGCGATGGGGGCGCGGAGCGCTGCCGGGAAGGAAGGAAGGAAACTGCAGCCCCCTCCCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6591012..6591150 26863196 MeRIP-seq:(Medium) rs1347488890 Functional Loss SNV dbSNP153 33..33 33 - - - 81344 RMVar_ID_81344 Human_SNP_ID_657110682 m1A Human chr19 - 6720595 6720595 6720595 GTCCCTCTGTCCCTCTGACCCTGCACTGTCCCAGCACCATGGGACCCACCTCAGGTCCCAGCCTG GTCCCTCTGTCCCTCTGACCCTGCACTGTCCCGGCACCATGGGACCCACCTCAGGTCCCAGCCTG T C C3 Ensembl:ENSG00000125730 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6720480..6720613 26863196 MeRIP-seq:(Medium) rs1273718812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771223,Human_RBP_ID_824826,Human_RBP_ID_914975,Human_RBP_ID_4557163,Human_RBP_ID_5239239,Human_RBP_ID_18944944,Human_RBP_ID_20432713,Human_RBP_ID_22447312 Human_Splice_Rec_1945271,Human_Splice_Rec_1945435 RMVar_hsa_circ_79185,RMVar_hsa_circ_191888 81345 RMVar_ID_81345 Human_SNP_ID_657113318 m1A Human chr19 + 6730479 6730479 6730479 CGGAACCACTCAGGCCCCGCCCCACTCCCCCCAACCACAGCAGCCCTGGCCTTGCCCACTCTACC CGGAACCACTCAGGCCCCGCCCCACTCCCCCCCACCACAGCAGCCCTGGCCTTGCCCACTCTACC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:6730377..6730619 26863196 MeRIP-seq:(Medium) rs1389168626 Functional Loss SNV dbSNP153 33..33 33 - - - 81346 RMVar_ID_81346 Human_SNP_ID_657114078 m1A Human chr19 - 6732376 6732376 6732376 ATCATCACGCCCTCCCCTGCTCCTTCAGGCTGAAGGGCGCCCTCCTCTTCATCACCATCGCCCTG ATCATCACGCCCTCCCCTGCTCCTTCAGGCTGGAGGGCGCCCTCCTCTTCATCACCATCGCCCTG T C GPR108 Ensembl:ENSG00000125734 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:6732251..6732375 32194978 MeRIP-seq:(Medium) rs917777992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1945468,Human_Splice_Rec_1945540,Human_Splice_Rec_1945574,Human_Splice_Rec_1945608,Human_Splice_Rec_1945624,Human_Splice_Rec_1945634 RMVar_hsa_circ_88810,RMVar_hsa_circ_96609,RMVar_hsa_circ_119751,RMVar_hsa_circ_191899,RMVar_hsa_circ_191900,RMVar_hsa_circ_191903,RMVar_hsa_circ_124140,RMVar_hsa_circ_370167,RMVar_hsa_circ_95065,RMVar_hsa_circ_191906,RMVar_hsa_circ_191907,RMVar_hsa_circ_191905,RMVar_hsa_circ_73393 81347 RMVar_ID_81347 Human_SNP_ID_657115702 m1A Human chr19 - 6736713 6736713 6736713 TCTGAACTGCCTCTGCCTCCTTGGTCTCCGGCAGGGGGAGAAGCGAGCGGACATCCAGCTGAACA TCTGAACTGCCTCTGCCTCCTTGGTCTCCGGCCGGGGGAGAAGCGAGCGGACATCCAGCTGAACA T G GPR108,MIR6791 Ensembl:ENSG00000125734,Ensembl:ENSG00000283950 Protein coding,miRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:6736606..6736763;chr19:6736674..6736779;chr19:6736676..6736762 26863196 MeRIP-seq:(Medium) rs182148180 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 81348 RMVar_ID_81348 Human_SNP_ID_657116008 m1A Human chr19 + 6737528 6737528 6737528 CAGCAGCAGCACCAGAAGTAGCCGCTGCCCCCACTCCGCGGGGCTCCCGCGGCCGAGCCCCCTCC CAGCAGCAGCACCAGAAGTAGCCGCTGCCCCCTCTCCGCGGGGCTCCCGCGGCCGAGCCCCCTCC A T - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:6737479..6737561 26863410 MeRIP-seq:(Medium) rs1233558787 Functional Loss SNV dbSNP153 33..33 33 - - - 81349 RMVar_ID_81349 Human_SNP_ID_657116710 m1A Human chr19 - 6739738 6739738 6739738 CCAATCCATGCTGCTCCCGCCGCCGCCGCCGCAGCCACCACCGCACCCGGTCCCCGCCGCCCGCC CCAATCCATGCTGCTCCCGCCGCCGCCGCCGCTGCCACCACCGCACCCGGTCCCCGCCGCCCGCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:6739676..6739821;chr19:6739676..6740720;chr19:6739701..6739844 26863196 MeRIP-seq:(Medium) rs747997121 Functional Loss SNV dbSNP153 33..33 33 - - - 81350 RMVar_ID_81350 Human_SNP_ID_657116711 m1A Human chr19 - 6739738 6739738 6739738 CCAATCCATGCTGCTCCCGCCGCCGCCGCCGCAGCCACCACCGCACCCGGTCCCCGCCGCCCGCC CCAATCCATGCTGCTCCCGCCGCCGCCGCCGCCGCCACCACCGCACCCGGTCCCCGCCGCCCGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:6739676..6739821;chr19:6739676..6740720;chr19:6739701..6739844 26863196 MeRIP-seq:(Medium) rs747997121 Functional Loss SNV dbSNP153 33..33 33 - - - 81351 RMVar_ID_81351 Human_SNP_ID_657116734 m1A Human chr19 + 6739774 6739774 6739774 GCGGCGGCGGCGGGAGCAGCATGGATTGGGGCACTGAGCTGTGGGTAAGTCCAATCGGCCCGCCT GCGGCGGCGGCGGGAGCAGCATGGATTGGGGCGCTGAGCTGTGGGTAAGTCCAATCGGCCCGCCT A G TRIP10 Ensembl:ENSG00000125733 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:6739690..6739779 26863410 MeRIP-seq:(Medium) rs1488665688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954297,Human_RBP_ID_5145624,Human_RBP_ID_8233594,Human_RBP_ID_9425158,Human_RBP_ID_18420840,Human_RBP_ID_18944952,Human_RBP_ID_18994166,Human_RBP_ID_24374469,Human_RBP_ID_24552921,Human_RBP_ID_26337206,Human_RBP_ID_26769782,Human_RBP_ID_27814993 Human_Splice_Rec_1945733,Human_Splice_Rec_1945759,Human_Splice_Rec_1945787,Human_Splice_Rec_1945815,Human_Splice_Rec_1945839 81352 RMVar_ID_81352 Human_SNP_ID_657117696 m1A Human chr19 + 6743090 6743090 6743090 CGTGTATGTCTTGAGCTGACCAAGTACTCACAAGAGATGAAACAGGAGAGGAAGATGGTGAGGAG CGTGTATGTCTTGAGCTGACCAAGTACTCACAGGAGATGAAACAGGAGAGGAAGATGGTGAGGAG A G TRIP10 Ensembl:ENSG00000125733 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6742951..6743167 26863196 MeRIP-seq:(Medium) rs1239215718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529117,Human_RBP_ID_3956116,Human_RBP_ID_26337208 Human_Splice_Rec_1945707,Human_Splice_Rec_1945739,Human_Splice_Rec_1945765,Human_Splice_Rec_1945793,Human_Splice_Rec_1945821,Human_Splice_Rec_1945845,Human_Splice_Rec_1945869,Human_Splice_Rec_1945883,Human_Splice_Rec_1945889,Human_Splice_Rec_1945897,Human_Splice_Rec_1945905 RMVar_hsa_circ_1075,RMVar_hsa_circ_280900,RMVar_hsa_circ_335963,RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_9332,RMVar_hsa_circ_191910,RMVar_hsa_circ_191911,RMVar_hsa_circ_191909 81353 RMVar_ID_81353 Human_SNP_ID_657117877 m1A Human chr19 + 6743545 6743545 6743545 GGGACTGCCGGGAGGCAGAGAAGGCAGCCCAGACTGCTGAACGGCTAGACCAGGATATCAACGCC GGGACTGCCGGGAGGCAGAGAAGGCAGCCCAGTCTGCTGAACGGCTAGACCAGGATATCAACGCC A T TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6743472..6743600 26863196 MeRIP-seq:(Medium) rs891743647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771225,Human_RBP_ID_825927,Human_RBP_ID_3954299,Human_RBP_ID_5116020,Human_RBP_ID_5191221,Human_RBP_ID_22661910,Human_RBP_ID_26335400 Human_Splice_Rec_1945710,Human_Splice_Rec_1945711,Human_Splice_Rec_1945742,Human_Splice_Rec_1945743,Human_Splice_Rec_1945768,Human_Splice_Rec_1945769,Human_Splice_Rec_1945796,Human_Splice_Rec_1945797,Human_Splice_Rec_1945824,Human_Splice_Rec_1945825,Human_Splice_Rec_1945848,Human_Splice_Rec_1945849,Human_Splice_Rec_1945872,Human_Splice_Rec_1945873,Human_Splice_Rec_1945885,Human_Splice_Rec_1945892,Human_Splice_Rec_1945893,Human_Splice_Rec_1945900,Human_Splice_Rec_1945901 RMVar_hsa_circ_1075,RMVar_hsa_circ_280900,RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_191910,RMVar_hsa_circ_191911 81354 RMVar_ID_81354 Human_SNP_ID_657118398 m1A Human chr19 + 6744902 6744902 6744902 TCAGCCAGCCCATGAACCGTGCACCCTCCGACAGCAGTCTGGGCACCCCCTCGGATGGACGGCCT TCAGCCAGCCCATGAACCGTGCACCCTCCGACTGCAGTCTGGGCACCCCCTCGGATGGACGGCCT A T TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6744853..6745099 26863196 MeRIP-seq:(Medium) rs763304765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771226,Human_RBP_ID_914206,Human_RBP_ID_9381812,Human_RBP_ID_18996284,Human_RBP_ID_26338364,Human_RBP_ID_27815932 Human_Splice_Rec_1945717,Human_Splice_Rec_1945749,Human_Splice_Rec_1945775,Human_Splice_Rec_1945803,Human_Splice_Rec_1945831,Human_Splice_Rec_1945855 RMVar_hsa_circ_1075,RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_191913,RMVar_hsa_circ_56838 81355 RMVar_ID_81355 Human_SNP_ID_657119075 m1A Human chr19 + 6746513 6746513 6746513 GCCCCCAGAGCAGCAGCGAAAACGGCTTCAACAGCAGTTGGAAGAACGCAGTCGTGAACTTCAGA GCCCCCAGAGCAGCAGCGAAAACGGCTTCAACGGCAGTTGGAAGAACGCAGTCGTGAACTTCAGA A G TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:6746287..6746525;chr19:6746370..6746534 26863196 MeRIP-seq:(Medium) rs901311261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8179,Human_RBP_ID_240009,Human_RBP_ID_529123,Human_RBP_ID_771229,Human_RBP_ID_5191223,Human_RBP_ID_5585964,Human_RBP_ID_26335405,Human_RBP_ID_27814998 Human_Splice_Rec_1945718,Human_Splice_Rec_1945719,Human_Splice_Rec_1945750,Human_Splice_Rec_1945751,Human_Splice_Rec_1945778,Human_Splice_Rec_1945779,Human_Splice_Rec_1945806,Human_Splice_Rec_1945807,Human_Splice_Rec_1945832,Human_Splice_Rec_1945833,Human_Splice_Rec_1945856,Human_Splice_Rec_1945857,Human_Splice_Rec_1945909 Human_miRNA_ID_2977820 RMVar_hsa_circ_1075,RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_191913 81356 RMVar_ID_81356 Human_SNP_ID_657119982 m1A Human chr19 - 6750032 6750032 6750032 CATACTTCTGCACTTCCAATTTCAGCCGTTCAATGTTGCTCAGGGTTTCAGCGATCTGGGGCTCC CATACTTCTGCACTTCCAATTTCAGCCGTTCAGTGTTGCTCAGGGTTTCAGCGATCTGGGGCTCC T C AC008760.1 Ensembl:ENSG00000269680 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6749982..6750101 26863196 MeRIP-seq:(Medium) rs544311636 Functional Loss SNV dbSNP153 33..33 33 - - - 81357 RMVar_ID_81357 Human_SNP_ID_657120079 m1A Human chr19 - 6750278 6750278 6750278 CAGCTTCTGCCAGCCACGCCTGGGAGGAGGGGACAGGAAAATCGTTCCAGGGCAGAGCTCCGGGG CAGCTTCTGCCAGCCACGCCTGGGAGGAGGGGGCAGGAAAATCGTTCCAGGGCAGAGCTCCGGGG T C AC008760.1 Ensembl:ENSG00000269680 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:6750276..6750325 32194978 MeRIP-seq:(Medium) rs1568256619 Functional Loss SNV dbSNP153 33..33 33 - - - 81358 RMVar_ID_81358 Human_SNP_ID_657120139 m1A Human chr19 + 6750379 6750379 6750379 GCCGGCACGCCCGGCCTCCCGACCCCCCCGCTAGCGCCCCGCCAGACAGCAGCAGCAACAGCGCA GCCGGCACGCCCGGCCTCCCGACCCCCCCGCTTGCGCCCCGCCAGACAGCAGCAGCAACAGCGCA A T TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6750301..6750625 26863196 MeRIP-seq:(Medium) rs534886687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529126,Human_RBP_ID_825934,Human_RBP_ID_5116618,Human_RBP_ID_17655488 Human_Splice_Rec_1945722,Human_Splice_Rec_1945723,Human_Splice_Rec_1945754,Human_Splice_Rec_1945755,Human_Splice_Rec_1945782,Human_Splice_Rec_1945783,Human_Splice_Rec_1945810,Human_Splice_Rec_1945811,Human_Splice_Rec_1945836,Human_Splice_Rec_1945860,Human_Splice_Rec_1945861,Human_Splice_Rec_1945912 RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_77437,RMVar_hsa_circ_191913,RMVar_hsa_circ_293256,RMVar_hsa_circ_317844,RMVar_hsa_circ_191914,RMVar_hsa_circ_362375 81359 RMVar_ID_81359 Human_SNP_ID_657120208 m1A Human chr19 + 6750541 6750541 6750541 CAGCTCTGAAGAGCCTCCCTCAGAAGAGAGCCAGGACACCCCCATTTACACGGAGTTTGATGAGG CAGCTCTGAAGAGCCTCCCTCAGAAGAGAGCCGGGACACCCCCATTTACACGGAGTTTGATGAGG A G TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6750267..6750636 26863196 MeRIP-seq:(Medium) rs373773172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27562928 Human_Splice_Rec_1945724,Human_Splice_Rec_1945725,Human_Splice_Rec_1945756,Human_Splice_Rec_1945757,Human_Splice_Rec_1945784,Human_Splice_Rec_1945785,Human_Splice_Rec_1945812,Human_Splice_Rec_1945813,Human_Splice_Rec_1945837,Human_Splice_Rec_1945862,Human_Splice_Rec_1945863 RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_191915,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_77437,RMVar_hsa_circ_191913,RMVar_hsa_circ_293256,RMVar_hsa_circ_317844,RMVar_hsa_circ_191914,RMVar_hsa_circ_337150 81360 RMVar_ID_81360 Human_SNP_ID_657121459 m1A Human chr19 - 6754278 6754278 6754278 GGGGCGGCGGGGGACCTGCCCGGGCTGGCTGCAGTCATGGGCGCCCTGCTCATGCCCCAGGTTCG GGGGCGGCGGGGGACCTGCCCGGGCTGGCTGCCGTCATGGGCGCCCTGCTCATGCCCCAGGTTCG T G SH2D3A Ensembl:ENSG00000125731 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:6754191..6754371 26863196 MeRIP-seq:(Medium) rs371546821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1945929,Human_Splice_Rec_1945959 81361 RMVar_ID_81361 Human_SNP_ID_657121522 m1A Human chr19 + 6754390 6754390 6754390 CGCGCTCCTCCAGCGGCCCCGAGCAGCCCAGCACCGCCAGCGCCCCGGCCAGCGCCAGTGTCTGA CGCGCTCCTCCAGCGGCCCCGAGCAGCCCAGCGCCGCCAGCGCCCCGGCCAGCGCCAGTGTCTGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6754143..6754438 26863196 MeRIP-seq:(Medium) rs368900527 Functional Loss SNV dbSNP153 33..33 33 - - - 81362 RMVar_ID_81362 Human_SNP_ID_657125171 m1A Human chr19 + 6767463 6767463 6767463 AAGCTGAGGCTCCGCGGCTCCGGGCTGCTGTCACCCCCGCCCTCCACCTTGCCACCGCCCCAGCC AAGCTGAGGCTCCGCGGCTCCGGGCTGCTGTCGCCCCCGCCCTCCACCTTGCCACCGCCCCAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6767354..6767491 26863196 MeRIP-seq:(Medium) rs1412062869 Functional Loss SNV dbSNP153 33..33 33 - - - 81363 RMVar_ID_81363 Human_SNP_ID_657211167 m1A Human chr19 - 7074977 7074977 7074977 CTCAGGACAGCACCCTGGAAGAAATGGGGGGAACACTCTGCCTCGGTCACCCCCTCCAGCCCGTG CTCAGGACAGCACCCTGGAAGAAATGGGGGGAGCACTCTGCCTCGGTCACCCCCTCCAGCCCGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7074896..7074995 26863196 MeRIP-seq:(Medium) rs142113377 Functional Loss SNV dbSNP153 33..33 33 - - - 81364 RMVar_ID_81364 Human_SNP_ID_657224675 m1A Human chr19 + 7122927 7122927 7122927 AGAGAACGGAGGTAGCTCTTCAGGTCTCCGTGAGCCATCAGCTCCATCACCACCAGCGTGGGCTG AGAGAACGGAGGTAGCTCTTCAGGTCTCCGTGGGCCATCAGCTCCATCACCACCAGCGTGGGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7122771..7122977 32194978 MeRIP-seq:(Medium) rs1337155856 Functional Loss SNV dbSNP153 33..33 33 - - - 81365 RMVar_ID_81365 Human_SNP_ID_657232141 m1A Human chr19 - 7151014 7151007 7151014 AATGAAAAAAAGAAGGAAGGAAAGAGAAAGAAAGCAAATGAAGGAAGGAAAGAGGGAAAAAGAGA AATGAAAAAAAGAAGGAAGGAAAGAGAAAGAA_______GAAGGAAGGAAAGAGGGAAAAAGAGA CATTTGCT C INSR Ensembl:ENSG00000171105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7150964..7151110 26863196 MeRIP-seq:(Medium) rs1449657639 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_2153,RMVar_hsa_circ_191933,RMVar_hsa_circ_123622,RMVar_hsa_circ_374962,RMVar_hsa_circ_68807,RMVar_hsa_circ_191938,RMVar_hsa_circ_79987,RMVar_hsa_circ_374746,RMVar_hsa_circ_191942,RMVar_hsa_circ_74773,RMVar_hsa_circ_191943,RMVar_hsa_circ_364304,RMVar_hsa_circ_114241,RMVar_hsa_circ_59051,RMVar_hsa_circ_106893,RMVar_hsa_circ_191944,RMVar_hsa_circ_191945,RMVar_hsa_circ_116342,RMVar_hsa_circ_365615,RMVar_hsa_circ_99705,RMVar_hsa_circ_191947,RMVar_hsa_circ_53137,RMVar_hsa_circ_191948,RMVar_hsa_circ_191949,RMVar_hsa_circ_315301,RMVar_hsa_circ_353912,RMVar_hsa_circ_7350,RMVar_hsa_circ_191950,RMVar_hsa_circ_191951 81366 RMVar_ID_81366 Human_SNP_ID_657233156 m1A Human chr19 + 7153138 7153127 7153138 AAACACACAACCACACACACACACCACACACCACACACACCACACAACACACCACACATACACAC AAACACACAACCACACACACAC___________CACACACCACACAACACACCACACATACACAC CACCACACACCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7153089..7153345 26863196 MeRIP-seq:(Medium) rs1568449343 Functional Loss DEL dbSNP153 23..33 33 - - - 81367 RMVar_ID_81367 Human_SNP_ID_657233170 m1A Human chr19 + 7153138 7153137 7153138 AAACACACAACCACACACACACACCACACACCACACACACCACACAACACACCACACATACACAC AAACACACAACCACACACACACACCACACACATCACACACCACACAACACACCACACATACACAC CA AT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7153089..7153345 26863196 MeRIP-seq:(Medium) rs796867273 Functional Loss MNV dbSNP153 32..33 33 - - - 81368 RMVar_ID_81368 Human_SNP_ID_657233172 m1A Human chr19 + 7153138 7153138 7153138 AAACACACAACCACACACACACACCACACACCACACACACCACACAACACACCACACATACACAC AAACACACAACCACACACACACACCACACACCCCACACACCACACAACACACCACACATACACAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7153089..7153345 26863196 MeRIP-seq:(Medium) rs1167153032 Functional Loss SNV dbSNP153 33..33 33 - - - 81369 RMVar_ID_81369 Human_SNP_ID_657245767 m1A Human chr19 + 7197616 7197616 7197616 GTGTGTGTGTGTGTGTCAGATTCCAGAGTGGGAGTGTGTGTGTGTTTGGCAGGTTCCAGAGTGGG GTGTGTGTGTGTGTGTCAGATTCCAGAGTGGGTGTGTGTGTGTGTTTGGCAGGTTCCAGAGTGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7197518..7197661 26863196 MeRIP-seq:(Medium) rs1321059600 Functional Loss SNV dbSNP153 33..33 33 - - - 81370 RMVar_ID_81370 Human_SNP_ID_657245826 m1A Human chr19 + 7197743 7197743 7197743 AGAGTGGGAGTGTGTGTGTGTGTGTGATTGGCAGGTTCCAGAGTGGGAGTGTGTGTGTGTGTGTG AGAGTGGGAGTGTGTGTGTGTGTGTGATTGGCCGGTTCCAGAGTGGGAGTGTGTGTGTGTGTGTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:7197741..7197838;chr19:7197683..7197767 26863196 MeRIP-seq:(Medium) rs28532199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23811088 81371 RMVar_ID_81371 Human_SNP_ID_657245881 m1A Human chr19 + 7197821 7197821 7197821 GATTGGTCGGTTCCAGAGTGGGAGAGAGAGCGAGAGAGAGAGAGAACGAGAGAGAGAGAGAGAGA GATTGGTCGGTTCCAGAGTGGGAGAGAGAGCGCGAGAGAGAGAGAACGAGAGAGAGAGAGAGAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7197818..7197911 26863196 MeRIP-seq:(Medium) rs886596077 Functional Loss SNV dbSNP153 33..33 33 - - - 81372 RMVar_ID_81372 Human_SNP_ID_657259175 m1A Human chr19 - 7247271 7247271 7247271 CAGAGAACAGTGCATTGCAGCTTAAGTGGAGTAAAATGGGTGTGGGTTTGGAGGAAGTGGATTAA CAGAGAACAGTGCATTGCAGCTTAAGTGGAGTGAAATGGGTGTGGGTTTGGAGGAAGTGGATTAA T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7247266..7247447 26863196 MeRIP-seq:(Medium) rs1186716293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3125,RMVar_hsa_circ_292925,RMVar_hsa_circ_191968,RMVar_hsa_circ_107734,RMVar_hsa_circ_351073,RMVar_hsa_circ_191967 81373 RMVar_ID_81373 Human_SNP_ID_657262552 m1A Human chr19 - 7259074 7259074 7259074 AAGGAAGGAGGGAAGGCGGGAAGGAAAGAAGGAGGGAAGGAGAAAGGAAGGAAGAAAGAAAGGAA AAGGAAGGAGGGAAGGCGGGAAGGAAAGAAGGCGGGAAGGAGAAAGGAAGGAAGAAAGAAAGGAA T G INSR Ensembl:ENSG00000171105 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7259071..7259215 26863196 MeRIP-seq:(Medium) rs372222109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3125,RMVar_hsa_circ_292925,RMVar_hsa_circ_191968,RMVar_hsa_circ_107734,RMVar_hsa_circ_351073,RMVar_hsa_circ_191967 81374 RMVar_ID_81374 Human_SNP_ID_657304896 m1A Human chr19 - 7419201 7419201 7419201 TACAGAGGCCGAGTGTGGGTACATCGGGGTACAGAGGCCGAGTGTGGGTACATCTGGGGTACAGA TACAGAGGCCGAGTGTGGGTACATCGGGGTACGGAGGCCGAGTGTGGGTACATCTGGGGTACAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:7419177..7419359 26863196 MeRIP-seq:(Medium) rs931349003 Functional Loss SNV dbSNP153 33..33 33 - - - 81375 RMVar_ID_81375 Human_SNP_ID_657304951 m1A Human chr19 + 7419292 7419284 7419292 GCACCCCAGGTGTGCCCACACTCGGCCCCCGCACCTGGGTGTGCCCACACTTGGCCCCCACACCC GCACCCCAGGTGTGCCCACACTCGG________CCTGGGTGTGCCCACACTTGGCCCCCACACCC GCCCCCGCA G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7419289..7419394 26863196 MeRIP-seq:(Medium) rs1211749564 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 81376 RMVar_ID_81376 Human_SNP_ID_657318746 m1A Human chr19 + 7467449 7467449 7467449 GCGCGAGCGCCAGTGGCAGCACCAGGAGCTGGAGCGTGCGGGCGCGCGGCTGCAGGAGCGCGAGG GCGCGAGCGCCAGTGGCAGCACCAGGAGCTGGTGCGTGCGGGCGCGCGGCTGCAGGAGCGCGAGG A T AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7467402..7467666 26863196 MeRIP-seq:(Medium) rs901784483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_852,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_191984 81377 RMVar_ID_81377 Human_SNP_ID_657325257 m1A Human chr19 - 7488924 7488924 7488924 CGCCTGGTGAGGCAGGGGCGGACCGGGGCCGGAGGTCCTAGAGTTTGGCCCAAGCTCAGAGACTG CGCCTGGTGAGGCAGGGGCGGACCGGGGCCGGGGGTCCTAGAGTTTGGCCCAAGCTCAGAGACTG T C PEX11G Ensembl:ENSG00000104883 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7488921..7488992 26863196 MeRIP-seq:(Medium) rs1019322747 Functional Loss SNV dbSNP153 33..33 33 - - - 81378 RMVar_ID_81378 Human_SNP_ID_657325335 m1A Human chr19 + 7489000 7489000 7489000 TGTACGACTCCAGCGCCGACGCCAGGCCGCTCAGCGACGCCATGGCAACTCCGTGACGTCACCGC TGTACGACTCCAGCGCCGACGCCAGGCCGCTCGGCGACGCCATGGCAACTCCGTGACGTCACCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7488902..7489008 26863196 MeRIP-seq:(Medium) rs1178310557 Functional Loss SNV dbSNP153 33..33 33 - - - 81379 RMVar_ID_81379 Human_SNP_ID_657329065 m1A Human chr19 + 7501312 7501312 7501312 ACCGCGACTCCCTGCCTCCTGGCGACCGCGACAAGTTGCGCATCCCGCCCACCACGCACCAGGCG ACCGCGACTCCCTGCCTCCTGGCGACCGCGACGAGTTGCGCATCCCGCCCACCACGCACCAGGCG A G TEX45 Ensembl:ENSG00000198723 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7501262..7501382 26863196 MeRIP-seq:(Medium) rs1462446860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1947015,Human_Splice_Rec_1947019,Human_Splice_Rec_1947037 81380 RMVar_ID_81380 Human_SNP_ID_657330199 m1A Human chr19 - 7505386 7505386 7505386 AGTGCTCGGCCTTGGTGGTCCTGTCGCGGAAGAGGCCGTCACCAGGACGGATATTTACACAGTGG AGTGCTCGGCCTTGGTGGTCCTGTCGCGGAAGGGGCCGTCACCAGGACGGATATTTACACAGTGG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7505336..7505491 26863196 MeRIP-seq:(Medium) rs1274349105 Functional Loss SNV dbSNP153 33..33 33 - - - 81381 RMVar_ID_81381 Human_SNP_ID_657330871 m1A Human chr19 - 7506983 7506983 7506983 CCGAGGCGGGGCTGAGGGTGTGGTGAAGTTCAAGGGAAGGGTTCAAGAGCCAAGCCCAGGCCAGC CCGAGGCGGGGCTGAGGGTGTGGTGAAGTTCAGGGGAAGGGTTCAAGAGCCAAGCCCAGGCCAGC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7506877..7507108 26863196 MeRIP-seq:(Medium) rs552858512 Functional Loss SNV dbSNP153 33..33 33 - - - 81382 RMVar_ID_81382 Human_SNP_ID_657333263 m1A Human chr19 + 7516145 7516145 7516145 CCCCGGGAGCGCCTGGCGGGGCCGCTGGGCCGAGGGGGCCGCCGGCGGGGCTGGCGGGCGGGGGG CCCCGGGAGCGCCTGGCGGGGCCGCTGGGCCGGGGGGGCCGCCGGCGGGGCTGGCGGGCGGGGGG A G ZNF358,AC008878.1 Ensembl:ENSG00000198816,Ensembl:ENSG00000267952 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:7516126..7516320 26863196 MeRIP-seq:(Medium) rs1183545134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559134,Human_RBP_ID_9353574 RMVar_hsa_circ_78724,RMVar_hsa_circ_191986 81383 RMVar_ID_81383 Human_SNP_ID_657333267 m1A Human chr19 - 7516164 7516164 7516164 CCCCCGGGCCCGCAGGAAGCCCCCCGCCCGCCAGCCCCGCCGGCGGCCCCCTCGGCCCAGCGGCC CCCCCGGGCCCGCAGGAAGCCCCCCGCCCGCCGGCCCCGCCGGCGGCCCCCTCGGCCCAGCGGCC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7516115..7516272 26863196 MeRIP-seq:(Medium) rs1048144635 Functional Loss SNV dbSNP153 33..33 33 - - - 81384 RMVar_ID_81384 Human_SNP_ID_657333268 m1A Human chr19 - 7516164 7516164 7516164 CCCCCGGGCCCGCAGGAAGCCCCCCGCCCGCCAGCCCCGCCGGCGGCCCCCTCGGCCCAGCGGCC CCCCCGGGCCCGCAGGAAGCCCCCCGCCCGCCCGCCCCGCCGGCGGCCCCCTCGGCCCAGCGGCC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7516115..7516272 26863196 MeRIP-seq:(Medium) rs1048144635 Functional Loss SNV dbSNP153 33..33 33 - - - 81385 RMVar_ID_81385 Human_SNP_ID_657334439 m1A Human chr19 - 7519547 7519547 7519547 GGGTGTCGCTGTTAGGATCGAGAATCAGGGGTACGGGGCCAATCACATCTGGATCGAGGTCGAAA GGGTGTCGCTGTTAGGATCGAGAATCAGGGGTGCGGGGCCAATCACATCTGGATCGAGGTCGAAA T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:7519426..7519622 26863410 MeRIP-seq:(Medium) rs1214676315 Functional Loss SNV dbSNP153 33..33 33 - - - 81386 RMVar_ID_81386 Human_SNP_ID_657334449 m1A Human chr19 + 7519570 7519570 7519570 TTGGCCCCGTACCCCTGATTCTCGATCCTAACAGCGACACCCTCAGCCCCGGCGATCCAAAAGTG TTGGCCCCGTACCCCTGATTCTCGATCCTAACGGCGACACCCTCAGCCCCGGCGATCCAAAAGTG A G ZNF358,AC008878.1 Ensembl:ENSG00000198816,Ensembl:ENSG00000267952 Protein coding,Protein coding CDS,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:7519201..7519750 26863196 MeRIP-seq:(Medium) rs767218388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18946404 RMVar_hsa_circ_78724,RMVar_hsa_circ_125513,RMVar_hsa_circ_191986,RMVar_hsa_circ_191987 81387 RMVar_ID_81387 Human_SNP_ID_657334742 m1A Human chr19 - 7520287 7520287 7520287 GCTCTGGCCGAAGGCCTTGGAGCAGTGCGGGCAGGCGTAGGGCCGCTCGCCCGTGTGGATGCGCA GCTCTGGCCGAAGGCCTTGGAGCAGTGCGGGCTGGCGTAGGGCCGCTCGCCCGTGTGGATGCGCA T A AC008878.4 Ensembl:ENSG00000269371 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7520236..7520343 26863196 MeRIP-seq:(Medium) rs1173852622 Functional Loss SNV dbSNP153 33..33 33 - - - 81388 RMVar_ID_81388 Human_SNP_ID_657335019 m1A Human chr19 + 7520772 7520772 7520772 CACGACGCTGGTCCCGACCTTGTGCCCAGCCCAGACCTTGATCCTGTGCCCAGCCCAGACCCTGA CACGACGCTGGTCCCGACCTTGTGCCCAGCCCCGACCTTGATCCTGTGCCCAGCCCAGACCCTGA A C ZNF358 Ensembl:ENSG00000198816 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7520751..7520775 26863196 MeRIP-seq:(Medium) rs1291462268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529281,Human_RBP_ID_5117303,Human_RBP_ID_5130992,Human_RBP_ID_17567538,Human_RBP_ID_18946407,Human_RBP_ID_23811207 Human_miRNA_ID_2555114 RMVar_hsa_circ_78724,RMVar_hsa_circ_125513,RMVar_hsa_circ_191986,RMVar_hsa_circ_191987 81389 RMVar_ID_81389 Human_SNP_ID_657335027 m1A Human chr19 + 7520780 7520780 7520780 TGGTCCCGACCTTGTGCCCAGCCCAGACCTTGATCCTGTGCCCAGCCCAGACCCTGATCCTGTGC TGGTCCCGACCTTGTGCCCAGCCCAGACCTTGTTCCTGTGCCCAGCCCAGACCCTGATCCTGTGC A T ZNF358 Ensembl:ENSG00000198816 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7520483..7520780 32194978 MeRIP-seq:(Medium) rs1214362367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529281,Human_RBP_ID_5117304,Human_RBP_ID_5130992,Human_RBP_ID_17567538,Human_RBP_ID_18946407,Human_RBP_ID_23811207 Human_miRNA_ID_2555115 RMVar_hsa_circ_78724,RMVar_hsa_circ_125513,RMVar_hsa_circ_191986,RMVar_hsa_circ_191987 81390 RMVar_ID_81390 Human_SNP_ID_657335053 m1A Human chr19 - 7520820 7520820 7520820 CAGGGGTCAGGGCAGGACACAGGGTTGGGATCAGGGCTGGGCACAGGATCAGGGTCTGGGCTGGG CAGGGGTCAGGGCAGGACACAGGGTTGGGATCTGGGCTGGGCACAGGATCAGGGTCTGGGCTGGG T A L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7520597..7520910 26863196 MeRIP-seq:(Medium) rs901362346 Functional Loss SNV dbSNP153 33..33 33 - - - 81391 RMVar_ID_81391 Human_SNP_ID_657335101 m1A Human chr19 + 7520928 7520928 7520928 GAGAGTCCAGAGTGGGTACAGGAGCAAGGGGCACTGCTGGGGCCTGATGGCTGAAGGAGACGCCG GAGAGTCCAGAGTGGGTACAGGAGCAAGGGGCGCTGCTGGGGCCTGATGGCTGAAGGAGACGCCG A G ZNF358 Ensembl:ENSG00000198816 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7520877..7520977 32194978 MeRIP-seq:(Medium) rs984399634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529289,Human_RBP_ID_3580761,Human_RBP_ID_4554440,Human_RBP_ID_6793580,Human_RBP_ID_17568892,Human_RBP_ID_17933782,Human_RBP_ID_18191915,Human_RBP_ID_27562936 RMVar_hsa_circ_78724,RMVar_hsa_circ_125513,RMVar_hsa_circ_191986,RMVar_hsa_circ_191987 81392 RMVar_ID_81392 Human_SNP_ID_657339343 m1A Human chr19 + 7534807 7534806 7534807 GTCCCAGTGATGCTCTGTGCCATAGAGCCCCCATAACTTCACTACTACGTGATAGTAAATCCCCG GTCCCAGTGATGCTCTGTGCCATAGAGCCCCC_TAACTTCACTACTACGTGATAGTAAATCCCCG CA C AC008878.2,PNPLA6 Ensembl:ENSG00000268614,Ensembl:ENSG00000032444 Protein coding,Protein coding 3'UTR,5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr19:7534719..7534874;chr19:7534764..7534900 26863196 MeRIP-seq:(Medium) rs1340517466 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1296295,Human_RBP_ID_1374634 Human_Splice_Rec_1947152,Human_Splice_Rec_1947153,Human_Splice_Rec_1947164,Human_Splice_Rec_1947165,Human_Splice_Rec_1947232,Human_Splice_Rec_1947236,Human_Splice_Rec_1947237,Human_Splice_Rec_1947250,Human_Splice_Rec_1947251,Human_Splice_Rec_1947266,Human_Splice_Rec_1947267,Human_Splice_Rec_1947329,Human_Splice_Rec_1947333,Human_Splice_Rec_1947397 81393 RMVar_ID_81393 Human_SNP_ID_657341790 m1A Human chr19 + 7542054 7542054 7542054 GCCCCTCTGCTGAGCCGCTGCGTCTCCATGCCAGGGGACATCTCAGGTTTGGAGCACTGGGTCTG GCCCCTCTGCTGAGCCGCTGCGTCTCCATGCCCGGGGACATCTCAGGTTTGGAGCACTGGGTCTG A C PNPLA6 Ensembl:ENSG00000032444 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:7541976..7542075 26863196 MeRIP-seq:(Medium) rs1462929521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1947186,Human_Splice_Rec_1947187,Human_Splice_Rec_1947288,Human_Splice_Rec_1947289,Human_Splice_Rec_1947354,Human_Splice_Rec_1947355,Human_Splice_Rec_1947420,Human_Splice_Rec_1947421,Human_Splice_Rec_1947502,Human_Splice_Rec_1947503,Human_Splice_Rec_1947582,Human_Splice_Rec_1947583,Human_Splice_Rec_1947592,Human_Splice_Rec_1947593 RMVar_hsa_circ_17569,RMVar_hsa_circ_110921,RMVar_hsa_circ_191992 81394 RMVar_ID_81394 Human_SNP_ID_657342001 m1A Human chr19 - 7542654 7542654 7542654 GGGTCCCAAGCCTTACCCGAGCGGGGGCTGCCAGGGACCCCCCGGAGGCCTCTTCCTGCAGGGAC GGGTCCCAAGCCTTACCCGAGCGGGGGCTGCCGGGGACCCCCCGGAGGCCTCTTCCTGCAGGGAC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:7542551..7542875 26863196 MeRIP-seq:(Medium) rs1430915125 Functional Loss SNV dbSNP153 33..33 33 - - - 81395 RMVar_ID_81395 Human_SNP_ID_657363874 m1A Human chr19 - 7613165 7613165 7613165 CCAGGACCCTCCAGCCACCTGCTCGGGGACTCACCTTGTAGAAGAACCCCAGCCCCACCCGGGGC CCAGGACCCTCCAGCCACCTGCTCGGGGACTCGCCTTGTAGAAGAACCCCAGCCCCACCCGGGGC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7613115..7613221 26863196 MeRIP-seq:(Medium) rs1289600071 Functional Loss SNV dbSNP153 33..33 33 - - - 81396 RMVar_ID_81396 Human_SNP_ID_657364582 m1A Human chr19 + 7615259 7615259 7615259 CCTGCTGGAGCGGCAGCAGCGGCGAGCAGAGGAGGCGCGGCGGCGCAAGCAGTGGCAGGAGGTGG CCTGCTGGAGCGGCAGCAGCGGCGAGCAGAGGCGGCGCGGCGGCGCAAGCAGTGGCAGGAGGTGG A C CAMSAP3 Ensembl:ENSG00000076826 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7615210..7615428 26863196 MeRIP-seq:(Medium) rs1568448240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239220 Human_Splice_Rec_1947668,Human_Splice_Rec_1947669,Human_Splice_Rec_1947704,Human_Splice_Rec_1947705,Human_Splice_Rec_1947715 RMVar_hsa_circ_192003,RMVar_hsa_circ_100733 81397 RMVar_ID_81397 Human_SNP_ID_657365812 m1A Human chr19 - 7618135 7618135 7618135 CACCCAGACACGGTTGGGGACAGACAGGACCCAGGAATACCGACTGACTGTCCTCCAGGGGATGG CACCCAGACACGGTTGGGGACAGACAGGACCCGGGAATACCGACTGACTGTCCTCCAGGGGATGG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7618085..7618153 26863196 MeRIP-seq:(Medium) rs550722498 Functional Loss SNV dbSNP153 33..33 33 - - - 81398 RMVar_ID_81398 Human_SNP_ID_657366779 m1A Human chr19 - 7620656 7620656 7620656 CCCCAACCCCGGTGTCCAGGTGCTGTCGGACGAGCACGCGCGTGAGATGTGCCTGCGGTTTGCAG CCCCAACCCCGGTGTCCAGGTGCTGTCGGACGTGCACGCGCGTGAGATGTGCCTGCGGTTTGCAG T A XAB2 Ensembl:ENSG00000076924 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7620607..7621033 32194978 MeRIP-seq:(Medium) rs1168841877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770086,Human_RBP_ID_8839684,Human_RBP_ID_9293286 Human_Splice_Rec_1947754,Human_Splice_Rec_1947778,Human_Splice_Rec_1947786 RMVar_hsa_circ_91906,RMVar_hsa_circ_113541,RMVar_hsa_circ_192004,RMVar_hsa_circ_97638,RMVar_hsa_circ_192005,RMVar_hsa_circ_112031,RMVar_hsa_circ_82042,RMVar_hsa_circ_192006,RMVar_hsa_circ_95608,RMVar_hsa_circ_192007,RMVar_hsa_circ_192008,RMVar_hsa_circ_192009 81399 RMVar_ID_81399 Human_SNP_ID_657369623 m1A Human chr19 - 7628276 7628276 7628276 GCCCTGGCAGGAGGAAGAGGACCTCCCCTATGAGGAGGAAATCATGCGGAACCAATTCTCTGTCA GCCCTGGCAGGAGGAAGAGGACCTCCCCTATGTGGAGGAAATCATGCGGAACCAATTCTCTGTCA T A XAB2 Ensembl:ENSG00000076924 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:7628226..7628300 32194978 MeRIP-seq:(Medium) rs1188259090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1296299,Human_RBP_ID_4557983,Human_RBP_ID_8496649,Human_RBP_ID_22449168 Human_Splice_Rec_1947728 RMVar_hsa_circ_192015,RMVar_hsa_circ_330607 81400 RMVar_ID_81400 Human_SNP_ID_657370522 m1A Human chr19 + 7631209 7631208 7631209 CCAGCCTGGGCAATAGAGTGAGACTTTGTCTCAAAAAGAAACATTTTACTCTCAGCCATGAGTAA CCAGCCTGGGCAATAGAGTGAGACTTTGTCTC_AAAAGAAACATTTTACTCTCAGCCATGAGTAA CA C PET100,AC008763.2 Ensembl:ENSG00000229833,Ensembl:ENSG00000268400 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7631205..7631328 26863196 MeRIP-seq:(Medium) rs1568457517 Functional Loss DEL dbSNP153 33..33 33 - - - 81401 RMVar_ID_81401 Human_SNP_ID_657370633 m1A Human chr19 - 7631412 7631412 7631412 AAGGGGGGAGGGGCACACACCTCAGAGCCGGGACCACCCCCCCCCGCCCACCTCTCCCACCACCC AAGGGGGGAGGGGCACACACCTCAGAGCCGGGGCCACCCCCCCCCGCCCACCTCTCCCACCACCC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:7631411..7631494;chr19:7631409..7631494 26863196 MeRIP-seq:(Medium) rs1206014191 Functional Loss SNV dbSNP153 33..33 33 - - - 81402 RMVar_ID_81402 Human_SNP_ID_657370634 m1A Human chr19 - 7631412 7631412 7631412 AAGGGGGGAGGGGCACACACCTCAGAGCCGGGACCACCCCCCCCCGCCCACCTCTCCCACCACCC AAGGGGGGAGGGGCACACACCTCAGAGCCGGGCCCACCCCCCCCCGCCCACCTCTCCCACCACCC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:7631411..7631494;chr19:7631409..7631494 26863196 MeRIP-seq:(Medium) rs1206014191 Functional Loss SNV dbSNP153 33..33 33 - - - 81403 RMVar_ID_81403 Human_SNP_ID_657370641 m1A Human chr19 - 7631426 7631426 7631426 GCGGGTGGGACAGGAAGGGGGGAGGGGCACACACCTCAGAGCCGGGACCACCCCCCCCCGCCCAC GCGGGTGGGACAGGAAGGGGGGAGGGGCACACCCCTCAGAGCCGGGACCACCCCCCCCCGCCCAC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7631424..7631550 26863196 MeRIP-seq:(Medium) rs1408408280 Functional Loss SNV dbSNP153 33..33 33 - - - 81404 RMVar_ID_81404 Human_SNP_ID_657372442 m1A Human chr19 + 7637185 7637185 7637185 GCGCCCTCGGGGCTGAAGGCGGTGGTGGGGGAAAGTGAGTGCCTCTCCGGGGCCGGGCTCTGGCG GCGCCCTCGGGGCTGAAGGCGGTGGTGGGGGAGAGTGAGTGCCTCTCCGGGGCCGGGCTCTGGCG A G STXBP2,AC008763.2 Ensembl:ENSG00000076944,Ensembl:ENSG00000268400 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7637134..7637230 26863196 MeRIP-seq:(Medium) rs765466426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3956140,Human_RBP_ID_4557986,Human_RBP_ID_18421632,Human_RBP_ID_23811267 Human_Splice_Rec_1947883,Human_Splice_Rec_1947885,Human_Splice_Rec_1947895,Human_Splice_Rec_1947931,Human_Splice_Rec_1947937,Human_Splice_Rec_1947973,Human_Splice_Rec_1947977,Human_Splice_Rec_1948013 81405 RMVar_ID_81405 Human_SNP_ID_657375567 m1A Human chr19 + 7643773 7643773 7643773 CTTGGAGAGGTGGGACCTGGGTGAGGGGTGGAACCTTGGAGAGGTGGGACCTGGATGAGGGGTGG CTTGGAGAGGTGGGACCTGGGTGAGGGGTGGAGCCTTGGAGAGGTGGGACCTGGATGAGGGGTGG A G STXBP2 Ensembl:ENSG00000076944 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:7643401..7643918 26863196 MeRIP-seq:(Medium) rs968114861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7484,Human_RBP_ID_263170,Human_RBP_ID_769481,Human_RBP_ID_3580769,Human_RBP_ID_3954336,Human_RBP_ID_5321351,Human_RBP_ID_5369874,Human_RBP_ID_8100310,Human_RBP_ID_8196041,Human_RBP_ID_8233068,Human_RBP_ID_8942409,Human_RBP_ID_9346669,Human_RBP_ID_9425928,Human_RBP_ID_19091959,Human_RBP_ID_21977609,Human_RBP_ID_22426326,Human_RBP_ID_22591014,Human_RBP_ID_22718311,Human_RBP_ID_26335422,Human_RBP_ID_27839249 RMVar_hsa_circ_126911,RMVar_hsa_circ_192017 81406 RMVar_ID_81406 Human_SNP_ID_657375788 m1A Human chr19 + 7644283 7644250 7644284 CCTCGGAGAGGTGGGACCTGGGTGAGGGGTGGAGCCTCGGAGAGCTGGGACCTGGGTGAGGGGTG __________________________________CCTCGGAGAGCTGGGACCTGGGTGAGGGGTG ACCTCGGAGAGGTGGGACCTGGGTGAGGGGTGGAG A STXBP2 Ensembl:ENSG00000076944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7644232..7644499 26863196 MeRIP-seq:(Medium) rs1568469523 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_8196046,Human_RBP_ID_21977613,Human_RBP_ID_22591015,Human_RBP_ID_26785242 RMVar_hsa_circ_126911,RMVar_hsa_circ_192017 81407 RMVar_ID_81407 Human_SNP_ID_657377126 m1A Human chr19 - 7647788 7647788 7647788 GGGCCAGGGGTCAGGGCAGGGCAATGTCCTCCAGCTTCTTGTCCAGTGCCTTCAGGTCATCCAGG GGGCCAGGGGTCAGGGCAGGGCAATGTCCTCCGGCTTCTTGTCCAGTGCCTTCAGGTCATCCAGG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7647700..7647821 26863196 MeRIP-seq:(Medium) rs1489364472 Functional Loss SNV dbSNP153 33..33 33 - - - 81408 RMVar_ID_81408 Human_SNP_ID_657386302 m1A Human chr19 - 7680880 7680878 7680880 CCCGGCGCGGGCAGGGGGGTGGGTAGGGTCTCACCAGGAACCGCAGCAGTCTGCTCGGCCGAGCT CCCGGCGCGGGCAGGGGGGTGGGTAGGGTCTC__CAGGAACCGCAGCAGTCTGCTCGGCCGAGCT GGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:7680826..7681011;chr19:7680826..7681087;chr19:7680826..7681067 26863196 MeRIP-seq:(Medium) rs1233904631 Functional Loss DEL dbSNP153 33..34 33 - - - 81409 RMVar_ID_81409 Human_SNP_ID_657431863 m1A Human chr19 + 7843040 7843038 7843041 GTGTATAGGTGTGTGAGCGTGTGTGTGAGAGAATAGGCATGGCTGTGTGTCGAGTATGTGCATGT GTGTATAGGTGTGTGAGCGTGTGTGTGAGAG___AGGCATGGCTGTGTGTCGAGTATGTGCATGT GAAT G EVI5L Ensembl:ENSG00000142459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7843034..7843810 26863196 MeRIP-seq:(Medium) rs1170251451 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_23811372 81410 RMVar_ID_81410 Human_SNP_ID_657431864 m1A Human chr19 + 7843039 7843038 7843039 TGTGTATAGGTGTGTGAGCGTGTGTGTGAGAGAATAGGCATGGCTGTGTGTCGAGTATGTGCATG TGTGTATAGGTGTGTGAGCGTGTGTGTGAGAG_ATAGGCATGGCTGTGTGTCGAGTATGTGCATG GA G EVI5L Ensembl:ENSG00000142459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7843035..7843691 26863196 MeRIP-seq:(Medium) rs1197169814 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23811372 81411 RMVar_ID_81411 Human_SNP_ID_657433151 m1A Human chr19 + 7846536 7846532 7846536 GTGAACCAACCCCGCTCACGGCTAACAAGCCCACCCACCATGGCGAGCCCCACTCTGAGCCCCGA GTGAACCAACCCCGCTCACGGCTAACAAG____CCCACCATGGCGAGCCCCACTCTGAGCCCCGA GCCCA G EVI5L Ensembl:ENSG00000142459 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7846446..7846635 26863196 MeRIP-seq:(Medium) rs1395356737 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_1948604 RMVar_hsa_circ_326115 81412 RMVar_ID_81412 Human_SNP_ID_657438094 m1A Human chr19 - 7863221 7863221 7863221 CTTGAGCTCGCGGATGTACTGCGATGAGTCCGAGTGGTTCAGCTGGCCCTGGATGCGGCCTTCCT CTTGAGCTCGCGGATGTACTGCGATGAGTCCGGGTGGTTCAGCTGGCCCTGGATGCGGCCTTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7863195..7864232 32194978 MeRIP-seq:(Medium) rs1167598026 Functional Loss SNV dbSNP153 33..33 33 - - - 81413 RMVar_ID_81413 Human_SNP_ID_657439700 m1A Human chr19 + 7868839 7868839 7868839 GGGCGTGTCCTAGGCCAAAGGGGCGGAGCTCGAGGGGCGGGCCTAGGTCAAAGCTGTGGGTAGGT GGGCGTGTCCTAGGCCAAAGGGGCGGAGCTCGGGGGGCGGGCCTAGGTCAAAGCTGTGGGTAGGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7868817..7868917 32194978 MeRIP-seq:(Medium) rs1286327882 Functional Loss SNV dbSNP153 33..33 33 - - - 81414 RMVar_ID_81414 Human_SNP_ID_657439889 m1A Human chr19 - 7869362 7869362 7869362 CGGCTGGGGCCGGGGCCGGGGCGTCCTCGCGGAGCCCGAAGCAGGCGCGCCTGGGCGAGCTGCCA CGGCTGGGGCCGGGGCCGGGGCGTCCTCGCGGGGCCCGAAGCAGGCGCGCCTGGGCGAGCTGCCA T C PRR36 Ensembl:ENSG00000183248 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7869315..7869517 26863196 MeRIP-seq:(Medium) rs1319492658 Functional Loss SNV dbSNP153 33..33 33 - - - 81415 RMVar_ID_81415 Human_SNP_ID_657440153 m1A Human chr19 - 7870082 7870082 7870082 TCTCCTTTGGCCACGCCTCCTCCACAGGCCCCACCTGTTCTGGCAGCGCCCCTTCTGCAGGTCCC TCTCCTTTGGCCACGCCTCCTCCACAGGCCCCGCCTGTTCTGGCAGCGCCCCTTCTGCAGGTCCC T C PRR36 Ensembl:ENSG00000183248 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7870078..7870185 32194978 MeRIP-seq:(Medium) rs1017630278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529356 81416 RMVar_ID_81416 Human_SNP_ID_657440919 m1A Human chr19 + 7871667 7871667 7871667 GAGAGGGAGAGGCCTGCAGAGGCAATGTGGCCAGAAGAGGAGAGTCCTGCAGAGGAAGAGTGGCC GAGAGGGAGAGGCCTGCAGAGGCAATGTGGCCGGAAGAGGAGAGTCCTGCAGAGGAAGAGTGGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7871654..7871820 26863196 MeRIP-seq:(Medium) rs1171692543 Functional Loss SNV dbSNP153 33..33 33 - - - 81417 RMVar_ID_81417 Human_SNP_ID_657441096 m1A Human chr19 + 7872080 7872080 7872080 GGTGGAACTTGCGAGGGGGGCGTGGCTGGTGGAGAGGGGAGGGTCTGCAGAGAAGGTGGAGCAGA GGTGGAACTTGCGAGGGGGGCGTGGCTGGTGGGGAGGGGAGGGTCTGCAGAGAAGGTGGAGCAGA A G NONHSAG024662.2 RNACentral:URS00008B87F3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7872044..7872137 26863196 MeRIP-seq:(Medium) rs1411230520 Functional Loss SNV dbSNP153 33..33 33 - - - 81418 RMVar_ID_81418 Human_SNP_ID_657441308 m1A Human chr19 - 7872571 7872571 7872571 AGCACAGTACCACCGAGCCAAGCCCGGCTGCCAGGAGGCGGCCCAGCGCCGGTGGGGGTCTCCAG AGCACAGTACCACCGAGCCAAGCCCGGCTGCCTGGAGGCGGCCCAGCGCCGGTGGGGGTCTCCAG T A PRR36 Ensembl:ENSG00000183248 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7872417..7873493 32194978 MeRIP-seq:(Medium) rs1332163123 Functional Loss SNV dbSNP153 33..33 33 - - - 81419 RMVar_ID_81419 Human_SNP_ID_657441542 m1A Human chr19 + 7873297 7873297 7873297 TCTCTCCCCTCTCCCAGAGGCTGGGGGCCTGGAGGCTGCGGGGAGAAGGCCGAGTCACAGGTGCC TCTCTCCCCTCTCCCAGAGGCTGGGGGCCTGGGGGCTGCGGGGAGAAGGCCGAGTCACAGGTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7873289..7873379 26863196 MeRIP-seq:(Medium) rs866254925 Functional Loss SNV dbSNP153 33..33 33 - - - 81420 RMVar_ID_81420 Human_SNP_ID_657441911 m1A Human chr19 - 7874330 7874330 7874330 GGCGGCCACCGCGTCGCTCCGGCCCGGGCCCCACCCCAGGCGACTCTGTGAGGAGCGGCCGGAGG GGCGGCCACCGCGTCGCTCCGGCCCGGGCCCCGCCCCAGGCGACTCTGTGAGGAGCGGCCGGAGG T C PRR36 Ensembl:ENSG00000183248 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7873591..7874379 32194978 MeRIP-seq:(Medium) rs1336524319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1948713 81421 RMVar_ID_81421 Human_SNP_ID_657452415 m1A Human chr19 - 7906158 7906158 7906158 CAACTTTCTCGTTCTCTCAGTTACACACACACAGGCGTGCACCCCCCCCACCCCCGGAGGCCACA CAACTTTCTCGTTCTCTCAGTTACACACACACGGGCGTGCACCCCCCCCACCCCCGGAGGCCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7906156..7906262 26863196 MeRIP-seq:(Medium) rs1425583448 Functional Loss SNV dbSNP153 33..33 33 - - - 81422 RMVar_ID_81422 Human_SNP_ID_657453180 m1A Human chr19 - 7908500 7908500 7908500 ACTGGTGCCCAGGGACTAATATGAACAGACAAACCCGCTCCATGCTGGCAGCTAAACCCCGTCCC ACTGGTGCCCAGGGACTAATATGAACAGACAACCCCGCTCCATGCTGGCAGCTAAACCCCGTCCC T G lnc-CTXN1-6 RNACentral:URS00008B24C8 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7908496..7908717 26863196 MeRIP-seq:(Medium) rs1001771176 Functional Loss SNV dbSNP153 33..33 33 - - - 81423 RMVar_ID_81423 Human_SNP_ID_657453625 m1A Human chr19 + 7909877 7909877 7909877 GCCACATGCTGGGGCTCCCGTCAACCCTGTTCACACCCCGCAGCATGGAGAGGTGAGCCAGGGGC GCCACATGCTGGGGCTCCCGTCAACCCTGTTCCCACCCCGCAGCATGGAGAGGTGAGCCAGGGGC A C MAP2K7 Ensembl:ENSG00000076984 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7909769..7910186 32194978 MeRIP-seq:(Medium) rs763099575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18742087 Human_Splice_Rec_1948759,Human_Splice_Rec_1948779,Human_Splice_Rec_1948799,Human_Splice_Rec_1948819 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81424 RMVar_ID_81424 Human_SNP_ID_657453626 m1A Human chr19 + 7909877 7909877 7909877 GCCACATGCTGGGGCTCCCGTCAACCCTGTTCACACCCCGCAGCATGGAGAGGTGAGCCAGGGGC GCCACATGCTGGGGCTCCCGTCAACCCTGTTCGCACCCCGCAGCATGGAGAGGTGAGCCAGGGGC A G MAP2K7 Ensembl:ENSG00000076984 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7909769..7910186 32194978 MeRIP-seq:(Medium) rs763099575 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18742087 Human_Splice_Rec_1948759,Human_Splice_Rec_1948779,Human_Splice_Rec_1948799,Human_Splice_Rec_1948819 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81425 RMVar_ID_81425 Human_SNP_ID_657455397 m1A Human chr19 + 7913418 7913418 7913418 CAGAGCAGGTGACCGGAGGGAATCGGTGACGGAGCGGGGCCAAGGGAGGGGTCCGGAGGGAGTCA CAGAGCAGGTGACCGGAGGGAATCGGTGACGGGGCGGGGCCAAGGGAGGGGTCCGGAGGGAGTCA A G MAP2K7 Ensembl:ENSG00000076984 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7913148..7913676 26863196 MeRIP-seq:(Medium) rs555837696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144988,Human_RBP_ID_6793724,Human_RBP_ID_8233414,Human_RBP_ID_9353685,Human_RBP_ID_21979003,Human_RBP_ID_23811452,Human_RBP_ID_26473405 Human_miRNA_ID_2218706 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81426 RMVar_ID_81426 Human_SNP_ID_657455398 m1A Human chr19 + 7913418 7913418 7913418 CAGAGCAGGTGACCGGAGGGAATCGGTGACGGAGCGGGGCCAAGGGAGGGGTCCGGAGGGAGTCA CAGAGCAGGTGACCGGAGGGAATCGGTGACGGTGCGGGGCCAAGGGAGGGGTCCGGAGGGAGTCA A T MAP2K7 Ensembl:ENSG00000076984 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7913148..7913676 26863196 MeRIP-seq:(Medium) rs555837696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144988,Human_RBP_ID_6793724,Human_RBP_ID_8233414,Human_RBP_ID_9353685,Human_RBP_ID_21979003,Human_RBP_ID_23811452,Human_RBP_ID_26473405 Human_miRNA_ID_2218706 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81427 RMVar_ID_81427 Human_SNP_ID_657455703 m1A Human chr19 + 7914169 7914169 7914169 CGAGGCCGGGCTGCCTGGTTTTATTTTTATTTAACTTTATTTTCTGTTTTATGAGTGTGTGTCCG CGAGGCCGGGCTGCCTGGTTTTATTTTTATTTCACTTTATTTTCTGTTTTATGAGTGTGTGTCCG A C MAP2K7 Ensembl:ENSG00000076984 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7914119..7914428 26863196 MeRIP-seq:(Medium) rs1312536184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6793743,Human_RBP_ID_17933877,Human_RBP_ID_23278911,Human_RBP_ID_23811460,Human_RBP_ID_26997560,Human_RBP_ID_27684471 Human_miRNA_ID_1752276,Human_miRNA_ID_2063923,Human_miRNA_ID_2901585 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81428 RMVar_ID_81428 Human_SNP_ID_657455759 m1A Human chr19 + 7914323 7914323 7914323 CCAGCCATCCCTCTGGACCAGGCAGAGGGCGGACCGGGTGGGCAGGGGCCTGAGGGTGGCTCGGG CCAGCCATCCCTCTGGACCAGGCAGAGGGCGGTCCGGGTGGGCAGGGGCCTGAGGGTGGCTCGGG A T MAP2K7 Ensembl:ENSG00000076984 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7914272..7914428 26863196 MeRIP-seq:(Medium) rs1462605077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529400,Human_RBP_ID_5144991,Human_RBP_ID_6793749,Human_RBP_ID_17933880,Human_RBP_ID_26473410 RMVar_hsa_circ_102366,RMVar_hsa_circ_192027 81429 RMVar_ID_81429 Human_SNP_ID_657456606 m1A Human chr19 + 7916778 7916778 7916778 CCTCTGTCGCCTTCCCGCCACCGCCGCCGCCGAGCCCGGGTGCCGCCCGCCCCGCGCGTTTCAGC CCTCTGTCGCCTTCCCGCCACCGCCGCCGCCGCGCCCGGGTGCCGCCCGCCCCGCGCGTTTCAGC A C TGFBR3L Ensembl:ENSG00000260001 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7916569..7917003 26863196 MeRIP-seq:(Medium) rs1309404494 Functional Loss SNV dbSNP153 33..33 33 - - - 81430 RMVar_ID_81430 Human_SNP_ID_657457351 m1A Human chr19 - 7919050 7919048 7919050 AGAGGTTTATTTTGAGCACAGGTGGGAGGGACAGGGGGAGGAGAGAAGCGCAGGGGTCGTGGCCT AGAGGTTTATTTTGAGCACAGGTGGGAGGGAC__GGGGAGGAGAGAAGCGCAGGGGTCGTGGCCT CCT C AC010336.2 Ensembl:ENSG00000260500 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr19:7918857..7919075;chr19:7918886..7919065 26863196 MeRIP-seq:(Medium) rs749809594 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_824322,Human_RBP_ID_3589351,Human_RBP_ID_4560385,Human_RBP_ID_8199700 81431 RMVar_ID_81431 Human_SNP_ID_657458495 m1A Human chr19 - 7922063 7922063 7922063 TGGGCTTGGGGGGCTTGGAGTGCAGGAGGGTGACCGGTTCCGTGGCCGCGATGGTGAGCACCTGG TGGGCTTGGGGGGCTTGGAGTGCAGGAGGGTGGCCGGTTCCGTGGCCGCGATGGTGAGCACCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7921477..7922300 26863196 MeRIP-seq:(Medium) rs1285737465 Functional Loss SNV dbSNP153 33..33 33 - - - 81432 RMVar_ID_81432 Human_SNP_ID_657458524 m1A Human chr19 + 7922099 7922099 7922099 CCTCCTGCACTCCAAGCCCCCCAAGCCCACGCAGGCCCGTGGAAAGCCTTTGCTCCTGAGCGCCC CCTCCTGCACTCCAAGCCCCCCAAGCCCACGCGGGCCCGTGGAAAGCCTTTGCTCCTGAGCGCCC A G SNAPC2 Ensembl:ENSG00000104976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7921527..7922300 26863196 MeRIP-seq:(Medium) rs1452160848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1948876,Human_Splice_Rec_1948884,Human_Splice_Rec_1948894,Human_Splice_Rec_1948900,Human_Splice_Rec_1948906 RMVar_hsa_circ_116935,RMVar_hsa_circ_192032 81433 RMVar_ID_81433 Human_SNP_ID_657458756 m1A Human chr19 + 7922494 7922494 7922494 GACCTGCTCATGTCACTTCCAGAGGAGCTGCCACTCCTGCCCTGCACAGCCCTGGTTGAGCATAT GACCTGCTCATGTCACTTCCAGAGGAGCTGCCGCTCCTGCCCTGCACAGCCCTGGTTGAGCATAT A G SNAPC2 Ensembl:ENSG00000104976 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7922349..7923150 32194978 MeRIP-seq:(Medium) rs1330645919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529408 Human_Splice_Rec_1948878,Human_Splice_Rec_1948902 RMVar_hsa_circ_116935,RMVar_hsa_circ_192032 81434 RMVar_ID_81434 Human_SNP_ID_657459800 m1A Human chr19 - 7925018 7925018 7925018 CATCTCACCCGCCCGGCTGGCCCCCACCCCCGACTCTGAATCCCGGGCGGGAGGAGGACCCCCGC CATCTCACCCGCCCGGCTGGCCCCCACCCCCGGCTCTGAATCCCGGGCGGGAGGAGGACCCCCGC T C CTXN1 Ensembl:ENSG00000178531 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:7924897..7925123 26863196 MeRIP-seq:(Medium) rs548483820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529428,Human_RBP_ID_5144993,Human_RBP_ID_9328553,Human_RBP_ID_21892104,Human_RBP_ID_23811476,Human_RBP_ID_27280258 81435 RMVar_ID_81435 Human_SNP_ID_657460219 m1A Human chr19 - 7926083 7926083 7926083 TCCGCCGCTCCAGGGGCGGGTGGGGTGGGCTGAGCCGGAGCCCGGGCCGCCGCCGCCGCCGCCGG TCCGCCGCTCCAGGGGCGGGTGGGGTGGGCTGGGCCGGAGCCCGGGCCGCCGCCGCCGCCGCCGG T C CTXN1 Ensembl:ENSG00000178531 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:7925501..7926100 26863196 MeRIP-seq:(Medium) rs1292628163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241870,Human_RBP_ID_4557994,Human_RBP_ID_5500385 81436 RMVar_ID_81436 Human_SNP_ID_657460220 m1A Human chr19 + 7926090 7926090 7926090 CGGCGGCGGCGGCCCGGGCTCCGGCTCAGCCCACCCCACCCGCCCCTGGAGCGGCGGAGACCGAG CGGCGGCGGCGGCCCGGGCTCCGGCTCAGCCCCCCCCACCCGCCCCTGGAGCGGCGGAGACCGAG A C AC010336.5 Ensembl:ENSG00000269139 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:7925997..7926112 26863410 MeRIP-seq:(Medium) rs973803640 Functional Loss SNV dbSNP153 33..33 33 - - - 81437 RMVar_ID_81437 Human_SNP_ID_657460566 m1A Human chr19 - 7926985 7926985 7926985 CGGGTGCGCGGCAGCTGGAGACACTCCCCCGCAGGGCCAACCCCTGCCCTGTTGCTCTGCCCTGC CGGGTGCGCGGCAGCTGGAGACACTCCCCCGCGGGGCCAACCCCTGCCCTGTTGCTCTGCCCTGC T C TIMM44 Ensembl:ENSG00000104980 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7926934..7927215 26863196 MeRIP-seq:(Medium) rs999332002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8496737,Human_RBP_ID_17656679,Human_RBP_ID_17933903,Human_RBP_ID_26471932,Human_RBP_ID_27280266 Human_miRNA_ID_939827,Human_miRNA_ID_2381478,Human_miRNA_ID_2427716,Human_miRNA_ID_3024487 RMVar_hsa_circ_86543,RMVar_hsa_circ_99792,RMVar_hsa_circ_114697,RMVar_hsa_circ_86962,RMVar_hsa_circ_192033,RMVar_hsa_circ_79296,RMVar_hsa_circ_82564,RMVar_hsa_circ_192035,RMVar_hsa_circ_192037,RMVar_hsa_circ_192038,RMVar_hsa_circ_192036,RMVar_hsa_circ_192034 81438 RMVar_ID_81438 Human_SNP_ID_657461045 m1A Human chr19 - 7928125 7928125 7928125 CAGCTGGCCCACCCCATCCAGCAGGCCAAGGCACTGGGTCTCCAGTTCCATTCTCGCATCCTAGA CAGCTGGCCCACCCCATCCAGCAGGCCAAGGCTCTGGGTCTCCAGTTCCATTCTCGCATCCTAGA T A TIMM44 Ensembl:ENSG00000104980 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:7928063..7928164 32194978 MeRIP-seq:(Medium) rs138623078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574441,Human_RBP_ID_4555071,Human_RBP_ID_6793768,Human_RBP_ID_22812935,Human_RBP_ID_26815158 Human_Splice_Rec_1948928,Human_Splice_Rec_1948929,Human_Splice_Rec_1948958,Human_Splice_Rec_1948959,Human_Splice_Rec_1948964,Human_Splice_Rec_1948965,Human_Splice_Rec_1948970,Human_Splice_Rec_1948971,Human_Splice_Rec_1948976,Human_Splice_Rec_1948996 RMVar_hsa_circ_86543,RMVar_hsa_circ_114697,RMVar_hsa_circ_86962,RMVar_hsa_circ_192033,RMVar_hsa_circ_79296,RMVar_hsa_circ_82564,RMVar_hsa_circ_192035,RMVar_hsa_circ_192037,RMVar_hsa_circ_192036,RMVar_hsa_circ_192034 81439 RMVar_ID_81439 Human_SNP_ID_657463549 m1A Human chr19 - 7935115 7935115 7935115 AGAAAACCATCGAGTCAGAAACCGTGCGGACGAGCGAGGTGCTACGGAAGAAGCTTGGGGAGCTG AGAAAACCATCGAGTCAGAAACCGTGCGGACGGGCGAGGTGCTACGGAAGAAGCTTGGGGAGCTG T C TIMM44 Ensembl:ENSG00000104980 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7935022..7935180 26863196 MeRIP-seq:(Medium) rs772993035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53085,Human_RBP_ID_6793835,Human_RBP_ID_8496772,Human_RBP_ID_9380255,Human_RBP_ID_13533640,Human_RBP_ID_18742147,Human_RBP_ID_18996391,Human_RBP_ID_21979683,Human_RBP_ID_26335440 Human_Splice_Rec_1948914,Human_Splice_Rec_1948915,Human_Splice_Rec_1948944,Human_Splice_Rec_1948945,Human_Splice_Rec_1948983,Human_Splice_Rec_1949006,Human_Splice_Rec_1949007,Human_Splice_Rec_1949022,Human_Splice_Rec_1949023 RMVar_hsa_circ_86543,RMVar_hsa_circ_192033,RMVar_hsa_circ_121957,RMVar_hsa_circ_352099,RMVar_hsa_circ_15771,RMVar_hsa_circ_192040 81440 RMVar_ID_81440 Human_SNP_ID_657464382 m1A Human chr19 - 7937985 7937985 7937985 TTTGCTGCTTTTTTTTCCCTCACCCAGGCTGGAGAGTAGTGGTGCGATCTCGGCTCACTGCAACC TTTGCTGCTTTTTTTTCCCTCACCCAGGCTGGGGAGTAGTGGTGCGATCTCGGCTCACTGCAACC T C TIMM44 Ensembl:ENSG00000104980 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7937982..7943671 26863196 MeRIP-seq:(Medium) rs1269029868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13533776,Human_RBP_ID_24485208 RMVar_hsa_circ_86543,RMVar_hsa_circ_192033,RMVar_hsa_circ_121957,RMVar_hsa_circ_15771,RMVar_hsa_circ_192040 81441 RMVar_ID_81441 Human_SNP_ID_657465839 m1A Human chr19 + 7943356 7943356 7943356 TTCTCTCTCCTGTATACGTGGAGTCTGATCAGAGGGCGAAGGGTGATCAGCTCCCTCCCAGGTCC TTCTCTCTCCTGTATACGTGGAGTCTGATCAGGGGGCGAAGGGTGATCAGCTCCCTCCCAGGTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7943354..7943638 26863196 MeRIP-seq:(Medium) rs965441600 Functional Loss SNV dbSNP153 33..33 33 - - - 81442 RMVar_ID_81442 Human_SNP_ID_657465885 m1A Human chr19 - 7943549 7943549 7943549 GGCGAGCTTAGGGGTCTTCTGGGCCTTCGGCCACCAAGGCTTTCTTCTCAGACCCTTGGCCTTCG GGCGAGCTTAGGGGTCTTCTGGGCCTTCGGCCGCCAAGGCTTTCTTCTCAGACCCTTGGCCTTCG T C TIMM44 Ensembl:ENSG00000104980 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7943548..7943641 26863196 MeRIP-seq:(Medium) rs1000583562 Functional Loss SNV dbSNP153 33..33 33 - - - 81443 RMVar_ID_81443 Human_SNP_ID_657466114 m1A Human chr19 - 7944059 7944059 7944059 CTGGAGCTGGTCCGCCGGTCAATCAGAATCCAATCGAATCCGTCCTTGTGGTCGGTGGATCCACG CTGGAGCTGGTCCGCCGGTCAATCAGAATCCAGTCGAATCCGTCCTTGTGGTCGGTGGATCCACG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7944026..7944144 26863196 MeRIP-seq:(Medium) rs564144503 Functional Loss SNV dbSNP153 33..33 33 - - - 81444 RMVar_ID_81444 Human_SNP_ID_657476855 m1A Human chr19 - 7984013 7984013 7984013 GTGGGTCCTCAGGGCCCATGGGTCTCCATGGAATGGACAGGGAGTGAGGAGCCTGAGGAGGGACA GTGGGTCCTCAGGGCCCATGGGTCTCCATGGAGTGGACAGGGAGTGAGGAGCCTGAGGAGGGACA T C ELAVL1 Ensembl:ENSG00000066044 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7984010..7984154 26863196 MeRIP-seq:(Medium) rs114721854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5238633,Human_RBP_ID_13534640,Human_RBP_ID_20433246 RMVar_hsa_circ_52168,RMVar_hsa_circ_364442,RMVar_hsa_circ_283037,RMVar_hsa_circ_363456 81445 RMVar_ID_81445 Human_SNP_ID_657478210 m1A Human chr19 + 7988938 7988938 7988938 AAGGGAAGGGAGGATCGGGGCTGGAGAGCTGGAGACGCTATTAGTTCCACTGCGAAGCGGGAGGT AAGGGAAGGGAGGATCGGGGCTGGAGAGCTGGGGACGCTATTAGTTCCACTGCGAAGCGGGAGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7988926..7989083 26863196 MeRIP-seq:(Medium) rs1304045129 Functional Loss SNV dbSNP153 33..33 33 - - - 81446 RMVar_ID_81446 Human_SNP_ID_657478913 m1A Human chr19 - 7991791 7991791 7991791 AAAATACAATGTCTAATGGTTATGAAGACCACATGGCCGAAGACTGCAGGGGTGACATCGGGAGA AAAATACAATGTCTAATGGTTATGAAGACCACGTGGCCGAAGACTGCAGGGGTGACATCGGGAGA T C ELAVL1 Ensembl:ENSG00000066044 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7991721..7991867 26863196 MeRIP-seq:(Medium) rs751134984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54881,Human_RBP_ID_908403,Human_RBP_ID_1574729,Human_RBP_ID_1893715,Human_RBP_ID_4560062,Human_RBP_ID_6794202,Human_RBP_ID_9380259,Human_RBP_ID_9929110,Human_RBP_ID_13534800,Human_RBP_ID_17656680,Human_RBP_ID_18192846,Human_RBP_ID_22069620,Human_RBP_ID_23811611,Human_RBP_ID_26816884,Human_RBP_ID_26997730,Human_RBP_ID_27815012 Human_Splice_Rec_1949034,Human_Splice_Rec_1949048,Human_Splice_Rec_1949058 RMVar_hsa_circ_52168,RMVar_hsa_circ_364442,RMVar_hsa_circ_283037,RMVar_hsa_circ_71163,RMVar_hsa_circ_363456 81447 RMVar_ID_81447 Human_SNP_ID_657481560 m1A Human chr19 - 8002242 8002242 8002242 GAGGAGGCAGTAGCGGTGGGGAGGAGCTAACCAGGCAAAGACAATAGGGTGGGGCTTTTTAGGAT GAGGAGGCAGTAGCGGTGGGGAGGAGCTAACCGGGCAAAGACAATAGGGTGGGGCTTTTTAGGAT T C ELAVL1 Ensembl:ENSG00000066044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8002238..8002325 26863196 MeRIP-seq:(Medium) rs902739967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5192852 81448 RMVar_ID_81448 Human_SNP_ID_657482585 m1A Human chr19 + 8005611 8005590 8005611 CGGTAGCGGTGGCGGCGGTGGCGGCGACGGCGACGGCGGCAGCGGCTCCTCCTCAGCGCGCACGA CGGTAGCGGTGG_____________________CGGCGGCAGCGGCTCCTCCTCAGCGCGCACGA GCGGCGGTGGCGGCGACGGCGA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h chr19:8005514..8005620;chr19:8005165..8005654 26863410,26863196 MeRIP-seq:(Medium) rs1352176807 Functional Loss DEL dbSNP153 13..33 33 - - - 81449 RMVar_ID_81449 Human_SNP_ID_657482589 m1A Human chr19 - 8005597 8005597 8005597 GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCACCGCCGCCACCGCTACCGAGGCCGAGCGGAGC GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCGCCGCCGCCACCGCTACCGAGGCCGAGCGGAGC T C ELAVL1 Ensembl:ENSG00000066044 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8005445..8005650 26863196 MeRIP-seq:(Medium) rs189171866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241088,Human_RBP_ID_529572,Human_RBP_ID_4555315,Human_RBP_ID_9293310,Human_RBP_ID_9328556,Human_RBP_ID_22533319 81450 RMVar_ID_81450 Human_SNP_ID_657482590 m1A Human chr19 - 8005597 8005597 8005597 GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCACCGCCGCCACCGCTACCGAGGCCGAGCGGAGC GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCCCCGCCGCCACCGCTACCGAGGCCGAGCGGAGC T G ELAVL1 Ensembl:ENSG00000066044 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8005445..8005650 26863196 MeRIP-seq:(Medium) rs189171866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241088,Human_RBP_ID_529572,Human_RBP_ID_4555315,Human_RBP_ID_9293310,Human_RBP_ID_9328556,Human_RBP_ID_22533319 81451 RMVar_ID_81451 Human_SNP_ID_657482601 m1A Human chr19 + 8005611 8005611 8005611 CGGTAGCGGTGGCGGCGGTGGCGGCGACGGCGACGGCGGCAGCGGCTCCTCCTCAGCGCGCACGA CGGTAGCGGTGGCGGCGGTGGCGGCGACGGCGGCGGCGGCAGCGGCTCCTCCTCAGCGCGCACGA A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h chr19:8005514..8005620;chr19:8005165..8005654 26863410,26863196 MeRIP-seq:(Medium) rs905884420 Functional Loss SNV dbSNP153 33..33 33 - - - 81452 RMVar_ID_81452 Human_SNP_ID_657482747 m1A Human chr19 - 8005908 8005908 8005908 ACAGGTGCGGGACACACGGCGAGCGCTCAACCAGAGGCGCCGCTCCTCAGCCACCGCCTTCCGTC ACAGGTGCGGGACACACGGCGAGCGCTCAACCGGAGGCGCCGCTCCTCAGCCACCGCCTTCCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8005872..8005957 26863196 MeRIP-seq:(Medium) rs576151303 Functional Loss SNV dbSNP153 33..33 33 - - - 81453 RMVar_ID_81453 Human_SNP_ID_657542832 m1A Human chr19 - 8209470 8209470 8209470 TCGCTTACCTGGGGGTGCAGGCGGCCGGGCGCACCGAGGGCCGGCGGCGGGGCTGGGGACGGCGC TCGCTTACCTGGGGGTGCAGGCGGCCGGGCGCGCCGAGGGCCGGCGGCGGGGCTGGGGACGGCGC T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8209420..8209534 26863196 MeRIP-seq:(Medium) rs960539630 Functional Loss SNV dbSNP153 33..33 33 - - - 81454 RMVar_ID_81454 Human_SNP_ID_657559162 m1A Human chr19 + 8262219 8262219 8262219 TGGGCCACCTTTCTGGAGACAGGGAGGGCCCCACCCGGGGTGGGTGGGAAGGCTGATGATCTGTC TGGGCCACCTTTCTGGAGACAGGGAGGGCCCCCCCCGGGGTGGGTGGGAAGGCTGATGATCTGTC A C CERS4 Ensembl:ENSG00000090661 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8262173..8262372 32194978 MeRIP-seq:(Medium) rs1336044474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557185,Human_RBP_ID_22448311,Human_RBP_ID_27472865 RMVar_hsa_circ_100360,RMVar_hsa_circ_192086 81455 RMVar_ID_81455 Human_SNP_ID_657568210 m1A Human chr19 - 8302797 8302797 8302797 TGCCGGAGACCAGTCTGGAAGCCCAACTGCCTATGGGGTTATTGCAGCTGCTGGTAAGAGGGACT TGCCGGAGACCAGTCTGGAAGCCCAACTGCCTGTGGGGTTATTGCAGCTGCTGGTAAGAGGGACT T C CD320 Ensembl:ENSG00000167775 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8302788..8302870 26863196 MeRIP-seq:(Medium) rs769747738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529673,Human_RBP_ID_4557187,Human_RBP_ID_5116640,Human_RBP_ID_22762708 Human_Splice_Rec_1949827,Human_Splice_Rec_1949833,Human_Splice_Rec_1949841,Human_Splice_Rec_1949849 Human_miRNA_ID_2280579,Human_miRNA_ID_2460643,Human_miRNA_ID_2640848 RMVar_hsa_circ_87046,RMVar_hsa_circ_122782,RMVar_hsa_circ_192089,RMVar_hsa_circ_76974,RMVar_hsa_circ_79249,RMVar_hsa_circ_192090,RMVar_hsa_circ_192091,RMVar_hsa_circ_192088 81456 RMVar_ID_81456 Human_SNP_ID_657568754 m1A Human chr19 - 8304082 8304082 8304082 GGGACCTGACCAACCCTGTGCCCCAGGGATTGAGCCATGTACCCAGAAAGGGCAATGCCCACCGC GGGACCTGACCAACCCTGTGCCCCAGGGATTGGGCCATGTACCCAGAAAGGGCAATGCCCACCGC T C CD320 Ensembl:ENSG00000167775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8303928..8304138 26863196 MeRIP-seq:(Medium) rs1011999624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529679,Human_RBP_ID_4557188,Human_RBP_ID_9329720,Human_RBP_ID_18470475,Human_RBP_ID_27562961 Human_Splice_Rec_1949830,Human_Splice_Rec_1949838 RMVar_hsa_circ_87046,RMVar_hsa_circ_122782,RMVar_hsa_circ_192090,RMVar_hsa_circ_192091,RMVar_hsa_circ_192092,RMVar_hsa_circ_43462 81457 RMVar_ID_81457 Human_SNP_ID_657570153 m1A Human chr19 - 8308249 8308249 8308249 GGTTGGATGGCGCAGGTTGGAGCGTGGCGAACAGGGGCTCTGGGCCTGGCGCTGCTGCTGCTGCT GGTTGGATGGCGCAGGTTGGAGCGTGGCGAACGGGGGCTCTGGGCCTGGCGCTGCTGCTGCTGCT T C CD320 Ensembl:ENSG00000167775 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr19:8308122..8308300;chr19:8308117..8308325 26863196,26863410 MeRIP-seq:(Medium) rs1336067266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772015,Human_RBP_ID_4557193,Human_RBP_ID_13535631,Human_RBP_ID_22447340,Human_RBP_ID_27472885 RMVar_hsa_circ_87046,RMVar_hsa_circ_192091 81458 RMVar_ID_81458 Human_SNP_ID_657570178 m1A Human chr19 + 8308279 8308279 8308279 CCTGTTCGCCACGCTCCAACCTGCGCCATCCAACCGCCGCTCATGCTGTCCCCACAGCGGCGCCG CCTGTTCGCCACGCTCCAACCTGCGCCATCCACCCGCCGCTCATGCTGTCCCCACAGCGGCGCCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:8308150..8308350;chr19:8308101..8308350;chr19:8308083..8308350;chr19:8308095..8308350 26863196 MeRIP-seq:(Medium) rs1479372765 Functional Loss SNV dbSNP153 33..33 33 - - - 81459 RMVar_ID_81459 Human_SNP_ID_657570193 m1A Human chr19 - 8308293 8308293 8308293 GGACAGCGCGTGGCCGGCGCCGCTGTGGGGACAGCATGAGCGGCGGTTGGATGGCGCAGGTTGGA GGACAGCGCGTGGCCGGCGCCGCTGTGGGGACGGCATGAGCGGCGGTTGGATGGCGCAGGTTGGA T C CD320,AC010323.1 Ensembl:ENSG00000167775,Ensembl:ENSG00000167774 Protein coding,Protein coding 5'UTR,3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1015910750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240584,Human_RBP_ID_4555526,Human_RBP_ID_17934076,Human_RBP_ID_22447340,Human_RBP_ID_23811796 RMVar_hsa_circ_87046,RMVar_hsa_circ_192091 81460 RMVar_ID_81460 Human_SNP_ID_657571125 m1A Human chr19 + 8311501 8311501 8311501 GAGGCAAAGTAGTCGGGTGGCCGTGAGGGTGCAGTGTCACAGGTAAGGCTGGTCCGAGGACAGCT GAGGCAAAGTAGTCGGGTGGCCGTGAGGGTGCGGTGTCACAGGTAAGGCTGGTCCGAGGACAGCT A G lnc-RPS28-1,lnc-RPS28-1:2 RNACentral:URS00008C1243,RNACentral:URS00009BFB7E lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8311451..8311525 26863196 MeRIP-seq:(Medium) rs779072206 Functional Loss SNV dbSNP153 33..33 33 - - - 81461 RMVar_ID_81461 Human_SNP_ID_657572537 m1A Human chr19 - 8316644 8316644 8316644 TTGCTTCAGTGCTCATCTTTTTTCCCCTCAGAACTCAGCCTCCTCCCAAGCTCCCTGTGGGTCCT TTGCTTCAGTGCTCATCTTTTTTCCCCTCAGATCTCAGCCTCCTCCCAAGCTCCCTGTGGGTCCT T A AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8316452..8316698 26863196 MeRIP-seq:(Medium) rs985572336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13535829,Human_RBP_ID_26815183 Human_Splice_Rec_1949858,Human_Splice_Rec_1949866,Human_Splice_Rec_1949882,Human_Splice_Rec_1949892 RMVar_hsa_circ_35369,RMVar_hsa_circ_300282 81462 RMVar_ID_81462 Human_SNP_ID_657573684 m1A Human chr19 - 8320860 8320860 8320860 GAAGCTGCAGCTACGCTACCAGGAGATCTCCAAGCGGTGAGCAGGCCCCGCTCGCTGCCCAGCCT GAAGCTGCAGCTACGCTACCAGGAGATCTCCAGGCGGTGAGCAGGCCCCGCTCGCTGCCCAGCCT T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr19:8320851..8320925;chr19:8320851..8321396 26863196,26863410 MeRIP-seq:(Medium) rs780963864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4555538,Human_RBP_ID_9090556,Human_RBP_ID_9381848,Human_RBP_ID_19091999,Human_RBP_ID_26815184 Human_Splice_Rec_1949856,Human_Splice_Rec_1949857,Human_Splice_Rec_1949864,Human_Splice_Rec_1949865,Human_Splice_Rec_1949872,Human_Splice_Rec_1949873,Human_Splice_Rec_1949878,Human_Splice_Rec_1949879,Human_Splice_Rec_1949890,Human_Splice_Rec_1949891 81463 RMVar_ID_81463 Human_SNP_ID_657573708 m1A Human chr19 - 8320905 8320905 8320905 CAGGCCGACCTCTCCTCTCCTCTTCCCACAGCATGACCTGCAGGGGAAGCTGCAGCTACGCTACC CAGGCCGACCTCTCCTCTCCTCTTCCCACAGCGTGACCTGCAGGGGAAGCTGCAGCTACGCTACC T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8320787..8320925 26863196 MeRIP-seq:(Medium) rs773718289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241815,Human_RBP_ID_4557194,Human_RBP_ID_5238636,Human_RBP_ID_5375563,Human_RBP_ID_8942416,Human_RBP_ID_9328557,Human_RBP_ID_9381848,Human_RBP_ID_22448323,Human_RBP_ID_22545548,Human_RBP_ID_22663601,Human_RBP_ID_25439307,Human_RBP_ID_26815185 Human_Splice_Rec_1949856,Human_Splice_Rec_1949857,Human_Splice_Rec_1949864,Human_Splice_Rec_1949865,Human_Splice_Rec_1949872,Human_Splice_Rec_1949873,Human_Splice_Rec_1949878,Human_Splice_Rec_1949879,Human_Splice_Rec_1949890,Human_Splice_Rec_1949891 81464 RMVar_ID_81464 Human_SNP_ID_657573882 m1A Human chr19 - 8321346 8321346 8321346 TTCAGTATCGCGGACGGAAGATGGCGTCCGCCACCCGTCTCATCCAGCGGCTGCGGAACTGGGCG TTCAGTATCGCGGACGGAAGATGGCGTCCGCCGCCCGTCTCATCCAGCGGCTGCGGAACTGGGCG T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8321206..8321375 26863196 MeRIP-seq:(Medium) rs781196681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529703,Human_RBP_ID_1296353,Human_RBP_ID_4557195,Human_RBP_ID_17386649,Human_RBP_ID_18420842 Human_Splice_Rec_1949855,Human_Splice_Rec_1949863,Human_Splice_Rec_1949871,Human_Splice_Rec_1949877,Human_Splice_Rec_1949889 81465 RMVar_ID_81465 Human_SNP_ID_657573883 m1A Human chr19 - 8321346 8321346 8321346 TTCAGTATCGCGGACGGAAGATGGCGTCCGCCACCCGTCTCATCCAGCGGCTGCGGAACTGGGCG TTCAGTATCGCGGACGGAAGATGGCGTCCGCCCCCCGTCTCATCCAGCGGCTGCGGAACTGGGCG T G AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8321206..8321375 26863196 MeRIP-seq:(Medium) rs781196681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529703,Human_RBP_ID_1296353,Human_RBP_ID_4557195,Human_RBP_ID_17386649,Human_RBP_ID_18420842 Human_Splice_Rec_1949855,Human_Splice_Rec_1949863,Human_Splice_Rec_1949871,Human_Splice_Rec_1949877,Human_Splice_Rec_1949889 81466 RMVar_ID_81466 Human_SNP_ID_657573897 m1A Human chr19 - 8321358 8321358 8321358 CCGGCTGCGCCCTTCAGTATCGCGGACGGAAGATGGCGTCCGCCACCCGTCTCATCCAGCGGCTG CCGGCTGCGCCCTTCAGTATCGCGGACGGAAGGTGGCGTCCGCCACCCGTCTCATCCAGCGGCTG T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding start codon,start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8321157..8321375 26863196 MeRIP-seq:(Medium) rs774726266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1296353,Human_RBP_ID_4557195,Human_RBP_ID_17386649,Human_RBP_ID_17934092,Human_RBP_ID_18420842,Human_RBP_ID_27280462 Human_Splice_Rec_1949855,Human_Splice_Rec_1949863,Human_Splice_Rec_1949871,Human_Splice_Rec_1949877,Human_Splice_Rec_1949889 81467 RMVar_ID_81467 Human_SNP_ID_657574044 m1A Human chr19 - 8321556 8321556 8321556 ATTCGGGCCCCCACCTCACCCTGGCCAGCTTGATAGGCTGCACACGGCTGGTGTCCATGATGGCG ATTCGGGCCCCCACCTCACCCTGGCCAGCTTGCTAGGCTGCACACGGCTGGTGTCCATGATGGCG T G lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:8321501..8321672 26863410 MeRIP-seq:(Medium) rs1411957341 Functional Loss SNV dbSNP153 33..33 33 - - - 81468 RMVar_ID_81468 Human_SNP_ID_657574132 m1A Human chr19 - 8321752 8321752 8321752 GCTGGCAGGGGTTAGGGCAGGGTAGAGGTCACATCAGGGTTTAGGTCGCCGGCAGTCGGCCAAAT GCTGGCAGGGGTTAGGGCAGGGTAGAGGTCACGTCAGGGTTTAGGTCGCCGGCAGTCGGCCAAAT T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8321582..8321943 26863196 MeRIP-seq:(Medium) rs1475093398 Functional Loss SNV dbSNP153 33..33 33 - - - 81469 RMVar_ID_81469 Human_SNP_ID_657587331 m1A Human chr19 - 8363414 8363414 8363414 AGGAAGGAAGGAGGGAAAGAAAGGAAGAAGGAAAGAAAGGAAGGAAAAGAAAAAGAGCTGAGTTC AGGAAGGAAGGAGGGAAAGAAAGGAAGAAGGAGAGAAAGGAAGGAAAAGAAAAAGAGCTGAGTTC T C lnc-KANK3-3,RAB11B-AS1 RNACentral:URS00008BE4EE,RNACentral:URS0000D58EB5 lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8363404..8363534 26863196 MeRIP-seq:(Medium) rs1013632744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25448661 81470 RMVar_ID_81470 Human_SNP_ID_657595499 m1A Human chr19 + 8390423 8390423 8390423 CCGATCCCGCCGGAAGCGCCAGGACAATGGGGACCCGGGACGACGAGTACGACTACCTATTCAAA CCGATCCCGCCGGAAGCGCCAGGACAATGGGGGCCCGGGACGACGAGTACGACTACCTATTCAAA A G RAB11B Ensembl:ENSG00000185236 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:8390376..8390603;chr19:8390376..8390570 26863196 MeRIP-seq:(Medium) rs768804811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1574834,Human_RBP_ID_4558010,Human_RBP_ID_5117318,Human_RBP_ID_9381849,Human_RBP_ID_22504091,Human_RBP_ID_26785263,Human_RBP_ID_27472898 Human_Splice_Rec_1950069,Human_Splice_Rec_1950077,Human_Splice_Rec_1950079,Human_Splice_Rec_1950083 81471 RMVar_ID_81471 Human_SNP_ID_657595513 m1A Human chr19 + 8390449 8390449 8390449 ATGGGGACCCGGGACGACGAGTACGACTACCTATTCAAAGGTGCGGCCGGTGGGGCACAGACGGG ATGGGGACCCGGGACGACGAGTACGACTACCTGTTCAAAGGTGCGGCCGGTGGGGCACAGACGGG A G RAB11B Ensembl:ENSG00000185236 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:8390376..8390625 26863410 MeRIP-seq:(Medium) rs373274971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529743,Human_RBP_ID_4558010,Human_RBP_ID_9381851,Human_RBP_ID_19089114,Human_RBP_ID_26785263 Human_Splice_Rec_1950069,Human_Splice_Rec_1950077,Human_Splice_Rec_1950079,Human_Splice_Rec_1950083 81472 RMVar_ID_81472 Human_SNP_ID_657595516 m1A Human chr19 - 8390458 8390458 8390458 ACGACTTCGCCCGTCTGTGCCCCACCGGCCGCACCTTTGAATAGGTAGTCGTACTCGTCGTCCCG ACGACTTCGCCCGTCTGTGCCCCACCGGCCGCCCCTTTGAATAGGTAGTCGTACTCGTCGTCCCG T G RAB11B-AS1 Ensembl:ENSG00000269386 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8390155..8390637 26863196 MeRIP-seq:(Medium) rs111785227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4555589,Human_RBP_ID_9381850,Human_RBP_ID_18742348 81473 RMVar_ID_81473 Human_SNP_ID_657595640 m1A Human chr19 + 8390779 8390779 8390779 GGGGCCTCCGCAGGGGGTGGAGCTTTCCCAAGATTTGGCGGGCCGGGCTGGGCTGAAAGCGTGAT GGGGCCTCCGCAGGGGGTGGAGCTTTCCCAAGGTTTGGCGGGCCGGGCTGGGCTGAAAGCGTGAT A G RAB11B Ensembl:ENSG00000185236 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8390777..8390966 26863196 MeRIP-seq:(Medium) rs375923248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196070,Human_RBP_ID_9427011 81474 RMVar_ID_81474 Human_SNP_ID_657597265 m1A Human chr19 + 8396519 8396519 8396519 TAATTCGGAGAGTAGAGTTTTAGTAGCATAGCAGGGAGGGCCTTCTTGGCCAAGTGGCATTTAAG TAATTCGGAGAGTAGAGTTTTAGTAGCATAGCCGGGAGGGCCTTCTTGGCCAAGTGGCATTTAAG A C RAB11B Ensembl:ENSG00000185236 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8396517..8396596 26863196 MeRIP-seq:(Medium) rs1253787364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3587853,Human_RBP_ID_13536085 81475 RMVar_ID_81475 Human_SNP_ID_657597371 m1A Human chr19 + 8396757 8396757 8396757 GGGAGGAGGGGAGGGCCCTGTGGGCAGCGGGGAGGACTGTGGCTTTTCCCCTGCGGAAGGTGGGG GGGAGGAGGGGAGGGCCCTGTGGGCAGCGGGGGGGACTGTGGCTTTTCCCCTGCGGAAGGTGGGG A G RAB11B Ensembl:ENSG00000185236 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8396755..8396901 26863196 MeRIP-seq:(Medium) rs1255871040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191250,Human_RBP_ID_9427013,Human_RBP_ID_26785267 81476 RMVar_ID_81476 Human_SNP_ID_657598186 m1A Human chr19 - 8399836 8399836 8399836 GCACCACTGGGCGGGAAGGCGAGGTTCTGTGAATCCCCACACTCCACCCACGACTGCCCCCACAA GCACCACTGGGCGGGAAGGCGAGGTTCTGTGACTCCCCACACTCCACCCACGACTGCCCCCACAA T G lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8399834..8400000 26863196 MeRIP-seq:(Medium) rs1020867542 Functional Loss SNV dbSNP153 33..33 33 - - - 81477 RMVar_ID_81477 Human_SNP_ID_657598210 m1A Human chr19 + 8399923 8399923 8399923 CAAGAGCAACCTGCTGTCGCGCTTCACCCGCAACGAGTTCAACCTGGAGAGCAAGAGCACCATCG CAAGAGCAACCTGCTGTCGCGCTTCACCCGCAGCGAGTTCAACCTGGAGAGCAAGAGCACCATCG A G RAB11B Ensembl:ENSG00000185236 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8390418..8400072 32194978 MeRIP-seq:(Medium) rs770191495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529744,Human_RBP_ID_1574840,Human_RBP_ID_8497032,Human_RBP_ID_13536095,Human_RBP_ID_18742351 Human_Splice_Rec_1950064,Human_Splice_Rec_1950070,Human_Splice_Rec_1950078,Human_Splice_Rec_1950084 RMVar_hsa_circ_110392,RMVar_hsa_circ_192103 81478 RMVar_ID_81478 Human_SNP_ID_657599275 m1A Human chr19 + 8403491 8403491 8403491 CCACGACGAGTCCCCGGGGAACAACGTGGTGGACATCAGCGTGCCGCCCACCACGGACGGACAGA CCACGACGAGTCCCCGGGGAACAACGTGGTGGCCATCAGCGTGCCGCCCACCACGGACGGACAGA A C RAB11B Ensembl:ENSG00000185236 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8403441..8403707 26863196 MeRIP-seq:(Medium) rs1483430107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1019284 Human_Splice_Rec_1950076 Human_miRNA_ID_2874149,Human_miRNA_ID_2982111 RMVar_hsa_circ_108277,RMVar_hsa_circ_110392,RMVar_hsa_circ_192103,RMVar_hsa_circ_192104 81479 RMVar_ID_81479 Human_SNP_ID_657599294 m1A Human chr19 - 8403536 8403536 8403536 GGCGCAGGGGTCACAGGTTCTGGCAGCACTGCAGCTTGTTGGGCTTCTGTCCGTCCGTGGTGGGC GGCGCAGGGGTCACAGGTTCTGGCAGCACTGCGGCTTGTTGGGCTTCTGTCCGTCCGTGGTGGGC T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8403420..8404250 26863196 MeRIP-seq:(Medium) rs1283032090 Functional Loss SNV dbSNP153 33..33 33 - - - 81480 RMVar_ID_81480 Human_SNP_ID_657599393 m1A Human chr19 - 8403794 8403794 8403794 CCCGTCCATCCTGCCGCCCTCCCCACCCCGCCAAGACGCTGTGGGGACCCGAGTTTCATGGGTGC CCCGTCCATCCTGCCGCCCTCCCCACCCCGCCTAGACGCTGTGGGGACCCGAGTTTCATGGGTGC T A lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:8403751..8404139 26863196 MeRIP-seq:(Medium) rs1301321407 Functional Loss SNV dbSNP153 33..33 33 - - - 81481 RMVar_ID_81481 Human_SNP_ID_657599514 m1A Human chr19 - 8404040 8404040 8404040 GGGAGGCCTGTGCGAGCTGCTGTGTGCGGAGGAGCGGGTGGGCGCTGAGAGCCCGGGGGGTCCGC GGGAGGCCTGTGCGAGCTGCTGTGTGCGGAGGTGCGGGTGGGCGCTGAGAGCCCGGGGGGTCCGC T A lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8404001..8404075 26863196 MeRIP-seq:(Medium) rs1256622406 Functional Loss SNV dbSNP153 33..33 33 - - - 81482 RMVar_ID_81482 Human_SNP_ID_657599555 m1A Human chr19 - 8404123 8404122 8404123 GGGCGCGTTGCGTGCAGGAGAGGGGAGGGGAGAGGGGAGAGGGGGGGACGGGCTTCTCCCTGCAT GGGCGCGTTGCGTGCAGGAGAGGGGAGGGGAG_GGGGAGAGGGGGGGACGGGCTTCTCCCTGCAT CT C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:8404023..8404124 26863410 MeRIP-seq:(Medium) rs1191918721 Functional Loss DEL dbSNP153 33..33 33 - - - 81483 RMVar_ID_81483 Human_SNP_ID_657599556 m1A Human chr19 - 8404123 8404123 8404123 GGGCGCGTTGCGTGCAGGAGAGGGGAGGGGAGAGGGGAGAGGGGGGGACGGGCTTCTCCCTGCAT GGGCGCGTTGCGTGCAGGAGAGGGGAGGGGAGGGGGGAGAGGGGGGGACGGGCTTCTCCCTGCAT T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:8404023..8404124 26863410 MeRIP-seq:(Medium) rs1280468027 Functional Loss SNV dbSNP153 33..33 33 - - - 81484 RMVar_ID_81484 Human_SNP_ID_657602334 m1A Human chr19 + 8413379 8413379 8413379 GCCGGGCCGGGCCGGGACCGGGGCCGAGGCGAACCGAGGGGCCTGTGCGGCCGCCCGGCCCGGCC GCCGGGCCGGGCCGGGACCGGGGCCGAGGCGAGCCGAGGGGCCTGTGCGGCCGCCCGGCCCGGCC A G MARCHF2 Ensembl:ENSG00000099785 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8413330..8413443 26863196 MeRIP-seq:(Medium) rs911896077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557198 Human_Splice_Rec_1950089,Human_Splice_Rec_1950095,Human_Splice_Rec_1950101,Human_Splice_Rec_1950107,Human_Splice_Rec_1950115 81485 RMVar_ID_81485 Human_SNP_ID_657603740 m1A Human chr19 - 8418492 8418491 8418492 AAAAGAAAGCAAGCAAACAAACAAACAAAAAAACAAATCTGAGCTCCAAAGTGGGGAGGTGAAGG AAAAGAAAGCAAGCAAACAAACAAACAAAAAA_CAAATCTGAGCTCCAAAGTGGGGAGGTGAAGG GT G lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8418490..8418563 26863196 MeRIP-seq:(Medium) rs1242459678 Functional Loss DEL dbSNP153 33..33 33 - - - 81486 RMVar_ID_81486 Human_SNP_ID_657606342 m1A Human chr19 - 8426693 8426693 8426693 AGCCACTTCTCCAGACAGCTCTTATGCACGGCACCCAGCGTGCCGGTGCAGCCACACGGGGACAG AGCCACTTCTCCAGACAGCTCTTATGCACGGCGCCCAGCGTGCCGGTGCAGCCACACGGGGACAG T C AC136469.1 Ensembl:ENSG00000268931 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8418766..8430833 32194978 MeRIP-seq:(Medium) rs1383667084 Functional Loss SNV dbSNP153 33..33 33 - - - 81487 RMVar_ID_81487 Human_SNP_ID_657609862 m1A Human chr19 + 8438892 8438892 8438892 CAAGGGCGCCCTTAAAGCTGGAACATTCCAGCAAGCTTCTTGCGCTTCTCTGCACCCGGCAGGCC CAAGGGCGCCCTTAAAGCTGGAACATTCCAGCTAGCTTCTTGCGCTTCTCTGCACCCGGCAGGCC A T MARCHF2 Ensembl:ENSG00000099785 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:8438844..8438924 32194978 MeRIP-seq:(Medium) rs73925332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_529788 81488 RMVar_ID_81488 Human_SNP_ID_657611579 m1A Human chr19 + 8445038 8445023 8445038 CAGGGGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGAGATCAAAATGGAGGAAGAGAGCGGCGCG CAGGGGTCGAAGCGGCGG_______________CGGAGATCAAAATGGAGGAAGAGAGCGGCGCG GCGGAGGTGGCGGCGA G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:8444926..8455615;chr19:8444976..8445159;chr19:8444906..8445179;chr19:8444976..8445161 26863196 MeRIP-seq:(Medium) rs764117449 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_54991,Human_RBP_ID_4555680,Human_RBP_ID_9380264,Human_RBP_ID_18165939,Human_RBP_ID_22241303,Human_RBP_ID_23114716,Human_RBP_ID_26335442,Human_RBP_ID_27815014 Human_Splice_Rec_1950135,Human_Splice_Rec_1950167,Human_Splice_Rec_1950173,Human_Splice_Rec_1950199,Human_Splice_Rec_1950229,Human_Splice_Rec_1950255,Human_Splice_Rec_1950281,Human_Splice_Rec_1950301,Human_Splice_Rec_1950315 81489 RMVar_ID_81489 Human_SNP_ID_657611582 m1A Human chr19 + 8445027 8445027 8445027 GAAAATGGCGGCAGGGGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGAGATCAAAATGGAGGAAG GAAAATGGCGGCAGGGGTCGAAGCGGCGGCGGGGGTGGCGGCGACGGAGATCAAAATGGAGGAAG A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8444976..8445149 26863196 MeRIP-seq:(Medium) rs767113114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54991,Human_RBP_ID_4555679,Human_RBP_ID_9380263,Human_RBP_ID_18165939,Human_RBP_ID_23114716,Human_RBP_ID_26335442,Human_RBP_ID_27815014 Human_Splice_Rec_1950135,Human_Splice_Rec_1950167,Human_Splice_Rec_1950173,Human_Splice_Rec_1950199,Human_Splice_Rec_1950229,Human_Splice_Rec_1950255,Human_Splice_Rec_1950281,Human_Splice_Rec_1950301,Human_Splice_Rec_1950315 81490 RMVar_ID_81490 Human_SNP_ID_657611592 m1A Human chr19 + 8445042 8445042 8445042 GGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGAGATCAAAATGGAGGAAGAGAGCGGCGCGCCCG GGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGCGATCAAAATGGAGGAAGAGAGCGGCGCGCCCG A C HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:8444976..8445181;chr19:8444898..8445169;chr19:8444915..8455629 26863196 MeRIP-seq:(Medium) rs748898936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54991,Human_RBP_ID_4555680,Human_RBP_ID_9380264,Human_RBP_ID_18165939,Human_RBP_ID_23114716,Human_RBP_ID_26335442,Human_RBP_ID_27815014 Human_Splice_Rec_1950135,Human_Splice_Rec_1950167,Human_Splice_Rec_1950173,Human_Splice_Rec_1950199,Human_Splice_Rec_1950229,Human_Splice_Rec_1950255,Human_Splice_Rec_1950281,Human_Splice_Rec_1950301,Human_Splice_Rec_1950315 81491 RMVar_ID_81491 Human_SNP_ID_657611593 m1A Human chr19 + 8445042 8445042 8445042 GGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGAGATCAAAATGGAGGAAGAGAGCGGCGCGCCCG GGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGGGATCAAAATGGAGGAAGAGAGCGGCGCGCCCG A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:8444976..8445181;chr19:8444898..8445169;chr19:8444915..8455629 26863196 MeRIP-seq:(Medium) rs748898936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54991,Human_RBP_ID_4555680,Human_RBP_ID_9380264,Human_RBP_ID_18165939,Human_RBP_ID_23114716,Human_RBP_ID_26335442,Human_RBP_ID_27815014 Human_Splice_Rec_1950135,Human_Splice_Rec_1950167,Human_Splice_Rec_1950173,Human_Splice_Rec_1950199,Human_Splice_Rec_1950229,Human_Splice_Rec_1950255,Human_Splice_Rec_1950281,Human_Splice_Rec_1950301,Human_Splice_Rec_1950315 81492 RMVar_ID_81492 Human_SNP_ID_657614624 m1A Human chr19 + 8455298 8455298 8455298 CCACCGCATCTGACCAATACTAGTCTTGTGTCATATGTAACTTTGTGTGGAATTGTAAACCTGGC CCACCGCATCTGACCAATACTAGTCTTGTGTCCTATGTAACTTTGTGTGGAATTGTAAACCTGGC A C HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8455292..8455475 26863196 MeRIP-seq:(Medium) rs541519689 Functional Loss SNV dbSNP153 33..33 33 - - - 81493 RMVar_ID_81493 Human_SNP_ID_657614625 m1A Human chr19 + 8455298 8455298 8455298 CCACCGCATCTGACCAATACTAGTCTTGTGTCATATGTAACTTTGTGTGGAATTGTAAACCTGGC CCACCGCATCTGACCAATACTAGTCTTGTGTCGTATGTAACTTTGTGTGGAATTGTAAACCTGGC A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8455292..8455475 26863196 MeRIP-seq:(Medium) rs541519689 Functional Loss SNV dbSNP153 33..33 33 - - - 81494 RMVar_ID_81494 Human_SNP_ID_657614629 m1A Human chr19 + 8455322 8455322 8455322 CTTGTGTCATATGTAACTTTGTGTGGAATTGTAAACCTGGCAAATCAAATAATTATCTTTCACAT CTTGTGTCATATGTAACTTTGTGTGGAATTGTTAACCTGGCAAATCAAATAATTATCTTTCACAT A T HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:8455319..8455475 26863196 MeRIP-seq:(Medium) rs1366361645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13536475 81495 RMVar_ID_81495 Human_SNP_ID_657614644 m1A Human chr19 - 8455367 8455367 8455367 TTCGAGAGAGAGGAAAAAAAGGTAAAGGGTTTATATGTCAGCACAATGTGAAAGATAATTATTTG TTCGAGAGAGAGGAAAAAAAGGTAAAGGGTTTGTATGTCAGCACAATGTGAAAGATAATTATTTG T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8455365..8455610 26863196 MeRIP-seq:(Medium) rs1284009512 Functional Loss SNV dbSNP153 33..33 33 - - - 81496 RMVar_ID_81496 Human_SNP_ID_657616722 m1A Human chr19 - 8463478 8463470 8463478 ACTTACGCACATCCCTTTGGAGGAAGCCAGAGACCAGTCAGAAGAGCAAGGAAGGGGAAAAAGAA ACTTACGCACATCCCTTTGGAGGAAGCCAGAG________GAAGAGCAAGGAAGGGGAAAAAGAA CTGACTGGT C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8463476..8463525 26863196 MeRIP-seq:(Medium) rs779325730 Functional Loss DEL dbSNP153 33..40 33 - - - 81497 RMVar_ID_81497 Human_SNP_ID_657616748 m1A Human chr19 - 8463551 8463551 8463551 CAAAAGGAAACGAGTCGAGTGAAACCAGTCCTACAAGTTAGAAGGCTCAAATACCAATAAGTAAC CAAAAGGAAACGAGTCGAGTGAAACCAGTCCTGCAAGTTAGAAGGCTCAAATACCAATAAGTAAC T C lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8463548..8463625 26863196 MeRIP-seq:(Medium) rs1305212205 Functional Loss SNV dbSNP153 33..33 33 - - - 81498 RMVar_ID_81498 Human_SNP_ID_657617943 m1A Human chr19 - 8467583 8467583 8467583 TATATCACAGAGAAAGATCCTACTGACTTACCATCTTGACGTGCATTGGTCTATCAAATAGCAGC TATATCACAGAGAAAGATCCTACTGACTTACCCTCTTGACGTGCATTGGTCTATCAAATAGCAGC T G lnc-KANK3-3 RNACentral:URS00008BE4EE lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:8467576..8467600 26863196 MeRIP-seq:(Medium) rs1309024378 Functional Loss SNV dbSNP153 33..33 33 - - - 81499 RMVar_ID_81499 Human_SNP_ID_657619055 m1A Human chr19 + 8471426 8471426 8471426 AAAGGCATCGGAATGGGAAACATAGGTCCCGCAGGTGAGAATGACAGTGCACCTTGCTTGGTGGT AAAGGCATCGGAATGGGAAACATAGGTCCCGCGGGTGAGAATGACAGTGCACCTTGCTTGGTGGT A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8471355..8471484 26863196 MeRIP-seq:(Medium) rs780614526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8497074,Human_RBP_ID_13537243,Human_RBP_ID_19089122,Human_RBP_ID_23811986,Human_RBP_ID_24374471 Human_Splice_Rec_1950155,Human_Splice_Rec_1950193,Human_Splice_Rec_1950217,Human_Splice_Rec_1950245,Human_Splice_Rec_1950269,Human_Splice_Rec_1950345,Human_Splice_Rec_1950355 RMVar_hsa_circ_8216,RMVar_hsa_circ_276241,RMVar_hsa_circ_307845,RMVar_hsa_circ_266612,RMVar_hsa_circ_192112,RMVar_hsa_circ_192111,RMVar_hsa_circ_346110,RMVar_hsa_circ_292107,RMVar_hsa_circ_192115,RMVar_hsa_circ_192116,RMVar_hsa_circ_287763,RMVar_hsa_circ_192119,RMVar_hsa_circ_192120,RMVar_hsa_circ_300095,RMVar_hsa_circ_368258,RMVar_hsa_circ_192123,RMVar_hsa_circ_103946,RMVar_hsa_circ_334894,RMVar_hsa_circ_192121,RMVar_hsa_circ_282662,RMVar_hsa_circ_192124,RMVar_hsa_circ_192125,RMVar_hsa_circ_192122,RMVar_hsa_circ_347837 81500 RMVar_ID_81500 Human_SNP_ID_657619746 m1A Human chr19 - 8473654 8473648 8473654 TCCTATGCCTTCCATTCCCATTCCTTAAAAAGAAAAAGTCAATGCAAACTAAAATTATGTCAAAG TCCTATGCCTTCCATTCCCATTCCTTAAAAAG______TCAATGCAAACTAAAATTATGTCAAAG ACTTTTT A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:8473651..8473725 26863196 MeRIP-seq:(Medium) rs760305459 Functional Loss DEL dbSNP153 33..38 33 - - - 81501 RMVar_ID_81501 Human_SNP_ID_657622366 m1A Human chr19 - 8482314 8482314 8482314 TCTCAAAGTATATGCTCAGCAACTTGGACATTAGCCACGAGGCACATTTCGCTTTATGACCACGG TCTCAAAGTATATGCTCAGCAACTTGGACATTGGCCACGAGGCACATTTCGCTTTATGACCACGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8482310..8482442 26863196 MeRIP-seq:(Medium) rs1276550606 Functional Loss SNV dbSNP153 33..33 33 - - - 81502 RMVar_ID_81502 Human_SNP_ID_657622590 m1A Human chr19 + 8483190 8483190 8483190 AAATCCTAAGTAATGCACTGAAGAGAGGAGAGATCATTGCAAAGCAGGGAGGAGGTAGGAACCGC AAATCCTAAGTAATGCACTGAAGAGAGGAGAGCTCATTGCAAAGCAGGGAGGAGGTAGGAACCGC A C HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8483151..8483225 26863196 MeRIP-seq:(Medium) rs1375603449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067461,Human_RBP_ID_3956167,Human_RBP_ID_6794930,Human_RBP_ID_8838623,Human_RBP_ID_13555151,Human_RBP_ID_22661969 Human_Splice_Rec_1950160,Human_Splice_Rec_1950161,Human_Splice_Rec_1950196,Human_Splice_Rec_1950197,Human_Splice_Rec_1950222,Human_Splice_Rec_1950223,Human_Splice_Rec_1950248,Human_Splice_Rec_1950249,Human_Splice_Rec_1950274,Human_Splice_Rec_1950275,Human_Splice_Rec_1950298,Human_Splice_Rec_1950299,Human_Splice_Rec_1950362,Human_Splice_Rec_1950363,Human_Splice_Rec_1950367 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 81503 RMVar_ID_81503 Human_SNP_ID_657623311 m1A Human chr19 - 8485604 8485599 8485605 CTCTCGATCCCAGGGACGCTTCCTCCACCTCCACCTGAAACAGGGACACAAAACACAGGTGGGTG CTCTCGATCCCAGGGACGCTTCCTCCACCTC______AAACAGGGACACAAAACACAGGTGGGTG TCAGGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:8485601..8485650 26863196 MeRIP-seq:(Medium) rs1416892676 Functional Loss DEL dbSNP153 32..37 33 - - - 81504 RMVar_ID_81504 Human_SNP_ID_657623313 m1A Human chr19 - 8485604 8485604 8485604 CTCTCGATCCCAGGGACGCTTCCTCCACCTCCACCTGAAACAGGGACACAAAACACAGGTGGGTG CTCTCGATCCCAGGGACGCTTCCTCCACCTCCGCCTGAAACAGGGACACAAAACACAGGTGGGTG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:8485601..8485650 26863196 MeRIP-seq:(Medium) rs1180687771 Functional Loss SNV dbSNP153 33..33 33 - - - 81505 RMVar_ID_81505 Human_SNP_ID_657623325 m1A Human chr19 - 8485652 8485631 8485652 ATGCGCTCCATGCCGGCACCCCCGAGGCGGTCAATGCCAGGACCCATCCTCTCGATCCCAGGGAC ATGCGCTCCATGCCGGCACCCCCGAGGCGGTC_____________________GATCCCAGGGAC CGAGAGGATGGGTCCTGGCATT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8483115..8486432 26863196 MeRIP-seq:(Medium) rs1568302162 Functional Loss DEL dbSNP153 33..53 33 - - - 81506 RMVar_ID_81506 Human_SNP_ID_657623333 m1A Human chr19 - 8485652 8485652 8485652 ATGCGCTCCATGCCGGCACCCCCGAGGCGGTCAATGCCAGGACCCATCCTCTCGATCCCAGGGAC ATGCGCTCCATGCCGGCACCCCCGAGGCGGTCCATGCCAGGACCCATCCTCTCGATCCCAGGGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8483115..8486432 26863196 MeRIP-seq:(Medium) rs867635055 Functional Loss SNV dbSNP153 33..33 33 - - - 81507 RMVar_ID_81507 Human_SNP_ID_657623362 m1A Human chr19 - 8485696 8485696 8485696 TCTCGGAGCCCACGCGATCCATGCCGTGGCCCAGGCCCGCGCCCATGCGCTCCATGCCGGCACCC TCTCGGAGCCCACGCGATCCATGCCGTGGCCCGGGCCCGCGCCCATGCGCTCCATGCCGGCACCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:8485601..8485850;chr19:8485571..8485825 26863196 MeRIP-seq:(Medium) rs1230284779 Functional Loss SNV dbSNP153 33..33 33 - - - 81508 RMVar_ID_81508 Human_SNP_ID_657623617 m1A Human chr19 + 8486151 8486127 8486151 AGCGGATGGGCCTGGAGCGCATGGGCGCCAACAGCCTCGAGCGCATGGGCCTGGAGCGCATGGGT AGCGGATGG________________________GCCTCGAGCGCATGGGCCTGGAGCGCATGGGT GGCCTGGAGCGCATGGGCGCCAACA G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:8486051..8486375 26863410 MeRIP-seq:(Medium) rs759817952 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_52916,Human_RBP_ID_1019301,Human_RBP_ID_4555777,Human_RBP_ID_5321379,Human_RBP_ID_17131636,Human_RBP_ID_22977877,Human_RBP_ID_26334814 Human_miRNA_ID_2716233,Human_miRNA_ID_3052218 RMVar_hsa_circ_266612,RMVar_hsa_circ_118381,RMVar_hsa_circ_269338,RMVar_hsa_circ_192128 81509 RMVar_ID_81509 Human_SNP_ID_657623633 m1A Human chr19 + 8486151 8486151 8486151 AGCGGATGGGCCTGGAGCGCATGGGCGCCAACAGCCTCGAGCGCATGGGCCTGGAGCGCATGGGT AGCGGATGGGCCTGGAGCGCATGGGCGCCAACGGCCTCGAGCGCATGGGCCTGGAGCGCATGGGT A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:8486051..8486375 26863410 MeRIP-seq:(Medium) rs1296674994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52916,Human_RBP_ID_1019301,Human_RBP_ID_4555777,Human_RBP_ID_5321379,Human_RBP_ID_17131636,Human_RBP_ID_22977877,Human_RBP_ID_26334814 Human_miRNA_ID_2716233,Human_miRNA_ID_3052218 RMVar_hsa_circ_266612,RMVar_hsa_circ_118381,RMVar_hsa_circ_269338,RMVar_hsa_circ_192128 81510 RMVar_ID_81510 Human_SNP_ID_657624563 m1A Human chr19 + 8488804 8488804 8488804 TGGCCGAGAGAGCCTGCCGGATGATGAATGGCATGAAGCTGAGTGGCCGAGAGATTGACGTTCGA TGGCCGAGAGAGCCTGCCGGATGATGAATGGCGTGAAGCTGAGTGGCCGAGAGATTGACGTTCGA A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:8488754..8488853 26863196 MeRIP-seq:(Medium) rs775738841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52920,Human_RBP_ID_1192229,Human_RBP_ID_1574892,Human_RBP_ID_1893852,Human_RBP_ID_3579145,Human_RBP_ID_4555798,Human_RBP_ID_5116040,Human_RBP_ID_8497103,Human_RBP_ID_8838641,Human_RBP_ID_9293048,Human_RBP_ID_13537793,Human_RBP_ID_17696712,Human_RBP_ID_17934840,Human_RBP_ID_18742416,Human_RBP_ID_22977239,Human_RBP_ID_23812054,Human_RBP_ID_26997942 RMVar_hsa_circ_118381,RMVar_hsa_circ_192128 81511 RMVar_ID_81511 Human_SNP_ID_657631625 m1A Human chr19 + 8510712 8510712 8510712 AGCGGCGGGATTCAGAGCTGCGAGAACACTGGAAGCTCCCCCTCTGACAGCAGCGGCGACACCTT AGCGGCGGGATTCAGAGCTGCGAGAACACTGGGAGCTCCCCCTCTGACAGCAGCGGCGACACCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8510662..8510761 26863196 MeRIP-seq:(Medium) rs1222273529 Functional Loss SNV dbSNP153 33..33 33 - - - 81512 RMVar_ID_81512 Human_SNP_ID_657631935 m1A Human chr19 - 8511528 8511528 8511528 ACTTGACCCGCCCCTTTACCGCAGGTGCTGGCAGCAGCCCCCGAAGACCCCAGGGCGGCTCCGAC ACTTGACCCGCCCCTTTACCGCAGGTGCTGGCTGCAGCCCCCGAAGACCCCAGGGCGGCTCCGAC T A ZNF414 Ensembl:ENSG00000133250 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8511464..8511563 32194978 MeRIP-seq:(Medium) rs1379173622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910498,Human_RBP_ID_5373123,Human_RBP_ID_19092020,Human_RBP_ID_23257707,Human_RBP_ID_26785270 Human_Splice_Rec_1950420,Human_Splice_Rec_1950421,Human_Splice_Rec_1950426,Human_Splice_Rec_1950427,Human_Splice_Rec_1950429,Human_Splice_Rec_1950436,Human_Splice_Rec_1950437,Human_Splice_Rec_1950442,Human_Splice_Rec_1950443,Human_Splice_Rec_1950454,Human_Splice_Rec_1950456 81513 RMVar_ID_81513 Human_SNP_ID_657632027 m1A Human chr19 + 8511734 8511734 8511734 GCCAAAGGGCGCAGGGTTCAAGTAGGGCAGGAACGGTCCGGTGGGGGCAGGGGCGGGGGTCGTGA GCCAAAGGGCGCAGGGTTCAAGTAGGGCAGGAGCGGTCCGGTGGGGGCAGGGGCGGGGGTCGTGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8511550..8511908 26863196 MeRIP-seq:(Medium) rs767631761 Functional Loss SNV dbSNP153 33..33 33 - - - 81514 RMVar_ID_81514 Human_SNP_ID_657632034 m1A Human chr19 - 8511743 8511743 8511743 TGGAACCCTTCACGACCCCCGCCCCTGCCCCCACCGGACCGTTCCTGCCCTACTTGAACCCTGCG TGGAACCCTTCACGACCCCCGCCCCTGCCCCCTCCGGACCGTTCCTGCCCTACTTGAACCCTGCG T A ZNF414 Ensembl:ENSG00000133250 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8511692..8511914 26863196 MeRIP-seq:(Medium) rs1301564725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116644,Human_RBP_ID_18946459 81515 RMVar_ID_81515 Human_SNP_ID_657632081 m1A Human chr19 - 8511811 8511811 8511811 GCCGCCCGCGCCGGAGCGCCCCCCGGAGGTTGACCCCGCATCAGCGCCGGGCCTGCCGTTCCCGC GCCGCCCGCGCCGGAGCGCCCCCCGGAGGTTGCCCCCGCATCAGCGCCGGGCCTGCCGTTCCCGC T G ZNF414 Ensembl:ENSG00000133250 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:8511759..8511859 26863410 MeRIP-seq:(Medium) rs958486384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4555812 81516 RMVar_ID_81516 Human_SNP_ID_657636945 m1A Human chr19 + 8526972 8526948 8526972 GGAGGGGCGGGTGAGAGCGTCAGGTGGGACACAGGTGAGGGCGACAGGTGAGAGAGACAGATGAA GGAGGGGCG________________________GGTGAGGGCGACAGGTGAGAGAGACAGATGAA GGGTGAGAGCGTCAGGTGGGACACA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8526922..8527075 26863196 MeRIP-seq:(Medium) rs756431782 Functional Loss DEL dbSNP153 10..33 33 - - - 81517 RMVar_ID_81517 Human_SNP_ID_657636953 m1A Human chr19 + 8526983 8526959 8526983 TGAGAGCGTCAGGTGGGACACAGGTGAGGGCGACAGGTGAGAGAGACAGATGAAGGTGGCTGAAG TGAGAGCGT________________________CAGGTGAGAGAGACAGATGAAGGTGGCTGAAG TCAGGTGGGACACAGGTGAGGGCGA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:8526746..8527384 26863196 MeRIP-seq:(Medium) rs1417605811 Functional Loss DEL dbSNP153 10..33 33 - - - 81518 RMVar_ID_81518 Human_SNP_ID_657660699 m1A Human chr19 + 8605215 8605204 8605215 CAGGAAGTGGGTGCTGGGCGAGGCCACTTTGTAGAAGAGGCGGGACTCGGCTGTGGCCCCCGTGC CAGGAAGTGGGTGCTGGGCGAG___________GAAGAGGCGGGACTCGGCTGTGGCCCCCGTGC GGCCACTTTGTA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8605164..8605350 26863196 MeRIP-seq:(Medium) rs1555742293 Functional Loss DEL dbSNP153 23..33 33 - - - 81519 RMVar_ID_81519 Human_SNP_ID_657660702 m1A Human chr19 - 8605212 8605212 8605212 CGGGGGCCACAGCCGAGTCCCGCCTCTTCTACAAAGTGGCCTCGCCCAGCACCCACTTCCTGCTG CGGGGGCCACAGCCGAGTCCCGCCTCTTCTACGAAGTGGCCTCGCCCAGCACCCACTTCCTGCTG T C ADAMTS10 Ensembl:ENSG00000142303 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:8605166..8605282 26863196 MeRIP-seq:(Medium) rs782650279 Functional Loss SNV dbSNP153 33..33 33 - - - 81520 RMVar_ID_81520 Human_SNP_ID_657660758 m1A Human chr19 - 8605314 8605314 8605314 CCAGTCTGGAGAGCTATGAGATCGCCTTCCCCACCCGCGTGGACCACAACGGGGCACTGCTGGCC CCAGTCTGGAGAGCTATGAGATCGCCTTCCCCGCCCGCGTGGACCACAACGGGGCACTGCTGGCC T C ADAMTS10 Ensembl:ENSG00000142303 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:8605276..8605350 26863196 MeRIP-seq:(Medium) rs1168401368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241682 Human_Splice_Rec_1950690,Human_Splice_Rec_1950762,Human_Splice_Rec_1950808,Human_Splice_Rec_1950852,Human_Splice_Rec_1950940,Human_Splice_Rec_1950948,Human_Splice_Rec_1950958 81521 RMVar_ID_81521 Human_SNP_ID_657660869 m1A Human chr19 + 8605634 8605634 8605634 CCACCACCAGACTTCCCCTACCTTGAGACCGGAAGGCGTGCGTGACCTCGAACATGAGGCCCAGC CCACCACCAGACTTCCCCTACCTTGAGACCGGCAGGCGTGCGTGACCTCGAACATGAGGCCCAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8605632..8605701 26863196 MeRIP-seq:(Medium) rs1047856554 Functional Loss SNV dbSNP153 33..33 33 - - - 81522 RMVar_ID_81522 Human_SNP_ID_657723893 m1A Human chr19 - 8823291 8823289 8823292 GTGTGGTCGGAGGACATGCGGTGAGAGAAAAAAGGAGTGAACGCCGTGGAAGTTGAGGAGGGAGG GTGTGGTCGGAGGACATGCGGTGAGAGAAAA___GAGTGAACGCCGTGGAAGTTGAGGAGGGAGG CCTT C ZNF558 Ensembl:ENSG00000167785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8822731..8823731 26863196 MeRIP-seq:(Medium) rs367883073 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_2678 81523 RMVar_ID_81523 Human_SNP_ID_657724190 m1A Human chr19 - 8823951 8823951 8823951 GGGACAGGGGAGGAGGTGTGAAGTTTAAAGAGAGGAGAGGAGGTTTGACGAGTGGGAAGCCATGC GGGACAGGGGAGGAGGTGTGAAGTTTAAAGAGCGGAGAGGAGGTTTGACGAGTGGGAAGCCATGC T G ZNF558 Ensembl:ENSG00000167785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:8823853..8823951 26863196 MeRIP-seq:(Medium) rs1297087394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5239244 RMVar_hsa_circ_2678 81524 RMVar_ID_81524 Human_SNP_ID_657726566 m1A Human chr19 + 8832549 8832549 8832549 GCGGGGGTAAGGTTGGCCCTGGGGGCGGGGCCAGGCTGTGAGCCGCACGAGGCCTGGGGGCGGGG GCGGGGGTAAGGTTGGCCCTGGGGGCGGGGCCGGGCTGTGAGCCGCACGAGGCCTGGGGGCGGGG A G MBD3L1 Ensembl:ENSG00000170948 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:8832510..8832581 26863196 MeRIP-seq:(Medium) rs557259178 Functional Loss SNV dbSNP153 33..33 33 - - - 81525 RMVar_ID_81525 Human_SNP_ID_657797426 m1A Human chr19 - 9044045 9044044 9044045 GCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAGGAAGGGAAAAAAAAAGCTCAGTTTCGGAGGT GCGACAGAGTGAGACTCTGTCTCAAAAAAAAA_GGAAGGGAAAAAAAAAGCTCAGTTTCGGAGGT CT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:9044019..9044106 26863410 MeRIP-seq:(Medium) rs991693169 Functional Loss DEL dbSNP153 33..33 33 - - - 81526 RMVar_ID_81526 Human_SNP_ID_657825621 m1A Human chr19 + 9140505 9140505 9140505 CTTTCGGCCTGTTGGGGACCCCTCGTGTCCCCACGCCAGACTGGACCTCCCGTATGAACTTCTCT CTTTCGGCCTGTTGGGGACCCCTCGTGTCCCCCCGCCAGACTGGACCTCCCGTATGAACTTCTCT A C ZNF317 Ensembl:ENSG00000130803 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr19:9140458..9140584;chr19:9140456..9140529 26863196 MeRIP-seq:(Medium) rs972911539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1951459,Human_Splice_Rec_1951469,Human_Splice_Rec_1951481,Human_Splice_Rec_1951493 81527 RMVar_ID_81527 Human_SNP_ID_657825657 m1A Human chr19 - 9140594 9140594 9140594 GAGGGGGAGAAGGGTTAAGGAAAGCAGGGCTTACACGACTGGGAATAGGATCGGGGGAGCGGAGG GAGGGGGAGAAGGGTTAAGGAAAGCAGGGCTTCCACGACTGGGAATAGGATCGGGGGAGCGGAGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:9140463..9140647 26863196 MeRIP-seq:(Medium) rs910426784 Functional Loss SNV dbSNP153 33..33 33 - - - 81528 RMVar_ID_81528 Human_SNP_ID_657827839 m1A Human chr19 + 9149578 9149578 9149578 AGGGGGCCAGGCACACTGAGAATGTGGGGGAAACATTTCAAGCAGAGGAGCAGCAGGTGCACAGA AGGGGGCCAGGCACACTGAGAATGTGGGGGAAGCATTTCAAGCAGAGGAGCAGCAGGTGCACAGA A G ZNF317 Ensembl:ENSG00000130803 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9149527..9149791 26863196 MeRIP-seq:(Medium) rs1053601123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5192862 81529 RMVar_ID_81529 Human_SNP_ID_657828848 m1A Human chr19 + 9153988 9153988 9153988 GGCATTGGTTTCAAGATGGGATAGACCTGAGCATGTGTCCATGCATAGGAAATTGTCTAGCAGGG GGCATTGGTTTCAAGATGGGATAGACCTGAGCGTGTGTCCATGCATAGGAAATTGTCTAGCAGGG A G ZNF317 Ensembl:ENSG00000130803 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9153938..9154199 26863196 MeRIP-seq:(Medium) rs1053301516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13538854 81530 RMVar_ID_81530 Human_SNP_ID_657828849 m1A Human chr19 + 9153988 9153988 9153988 GGCATTGGTTTCAAGATGGGATAGACCTGAGCATGTGTCCATGCATAGGAAATTGTCTAGCAGGG GGCATTGGTTTCAAGATGGGATAGACCTGAGCTTGTGTCCATGCATAGGAAATTGTCTAGCAGGG A T ZNF317 Ensembl:ENSG00000130803 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9153938..9154199 26863196 MeRIP-seq:(Medium) rs1053301516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13538854 81531 RMVar_ID_81531 Human_SNP_ID_657830544 m1A Human chr19 + 9160261 9160261 9160261 ACCGCCGCGACTATGGGGTAGCGTTCAAGGGCAGGCCGCACCTCACTCAGCACATGAGCATGTAC ACCGCCGCGACTATGGGGTAGCGTTCAAGGGCTGGCCGCACCTCACTCAGCACATGAGCATGTAC A T ZNF317 Ensembl:ENSG00000130803 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:9160211..9160471 26863196 MeRIP-seq:(Medium) rs1447825799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908411,Human_RBP_ID_8497198,Human_RBP_ID_18742612,Human_RBP_ID_26337270 Human_miRNA_ID_190133 81532 RMVar_ID_81532 Human_SNP_ID_657830848 m1A Human chr19 + 9161023 9161023 9161023 ATCTCTGCGGGAAAGCTTTCAGCGCGAGTTCAAACCTCACCGCACACAGGAAGATACACACGCAA ATCTCTGCGGGAAAGCTTTCAGCGCGAGTTCAGACCTCACCGCACACAGGAAGATACACACGCAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1455924010 Functional Loss SNV dbSNP153 33..33 33 - - - 81533 RMVar_ID_81533 Human_SNP_ID_657868673 m1A Human chr19 + 9309680 9309680 9309680 CGGACAAGGAGTGGCGGGGAGGCAGCCCTTAGACCGCCGATTCCCAAACCCAGCCCTCGGTCTCC CGGACAAGGAGTGGCGGGGAGGCAGCCCTTAGCCCGCCGATTCCCAAACCCAGCCCTCGGTCTCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:9309585..9309718 26863196 MeRIP-seq:(Medium) rs997056900 Functional Loss SNV dbSNP153 33..33 33 - - - 81534 RMVar_ID_81534 Human_SNP_ID_657903844 m1A Human chr19 - 9430442 9430442 9430442 GTTGGATAGGCAAGGCTGGAGGTCAAGATAGAAAGTGAGAAGGGTAGTAGTGTTGCGGGACGATC GTTGGATAGGCAAGGCTGGAGGTCAAGATAGAGAGTGAGAAGGGTAGTAGTGTTGCGGGACGATC T C ZNF266 Ensembl:ENSG00000174652 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:9430362..9430544 26863196 MeRIP-seq:(Medium) rs970559271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13540233 RMVar_hsa_circ_192199,RMVar_hsa_circ_102667,RMVar_hsa_circ_117157,RMVar_hsa_circ_192201,RMVar_hsa_circ_376310,RMVar_hsa_circ_192204,RMVar_hsa_circ_192205,RMVar_hsa_circ_104551 81535 RMVar_ID_81535 Human_SNP_ID_657907727 m1A Human chr19 + 9444660 9444660 9444660 GAAAGAAAGAAAGAGAGAAGGGGGGGAGAAGAAAGAAAGAAACAAAGAGAAAAGAACGAGGAAAG GAAAGAAAGAAAGAGAGAAGGGGGGGAGAAGAGAGAAAGAAACAAAGAGAAAAGAACGAGGAAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9444657..9444798 26863196 MeRIP-seq:(Medium) rs539149244 Functional Loss SNV dbSNP153 33..33 33 - - - 81536 RMVar_ID_81536 Human_SNP_ID_657939380 m1A Human chr19 - 9561636 9561636 9561636 GCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCCAGGATTACAGGTGTGAGCCACCACACCCAGTCC GCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGCCACCACACCCAGTCC T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1339472372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141201 81537 RMVar_ID_81537 Human_SNP_ID_657956711 m1A Human chr19 - 9621107 9621107 9621107 TCCCGGGGATAGCAGGGGGCGGCAAAGGAATGATTGCGCGCTGTCGCCTAGGAGCCTCTCAGATC TCCCGGGGATAGCAGGGGGCGGCAAAGGAATGGTTGCGCGCTGTCGCCTAGGAGCCTCTCAGATC T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:9621070..9621179 26863196 MeRIP-seq:(Medium) rs1421766236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_121462,RMVar_hsa_circ_192226 81538 RMVar_ID_81538 Human_SNP_ID_657956735 m1A Human chr19 + 9621174 9621173 9621175 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGC__ACTCCACCACCATAAAGGCGAAACCGCACTG CAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs1409356487 Functional Loss DEL dbSNP153 33..34 33 - - - 81539 RMVar_ID_81539 Human_SNP_ID_657956739 m1A Human chr19 + 9621174 9621173 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGAGGACTCCACCACCATAAAGGCGAAACCGCACTG CA AG - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs386806717 Functional Loss MNV dbSNP153 32..33 33 - - - 81540 RMVar_ID_81540 Human_SNP_ID_657956740 m1A Human chr19 + 9621174 9621173 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGGGGACTCCACCACCATAAAGGCGAAACCGCACTG CA GG - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs386806717 Functional Loss MNV dbSNP153 32..33 33 - - - 81541 RMVar_ID_81541 Human_SNP_ID_657956741 m1A Human chr19 + 9621174 9621174 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGCCGACTCCACCACCATAAAGGCGAAACCGCACTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs10401707 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9603,GWAS_ID_9604,GWAS_ID_9605 81542 RMVar_ID_81542 Human_SNP_ID_657956742 m1A Human chr19 + 9621174 9621174 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGCGGACTCCACCACCATAAAGGCGAAACCGCACTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs10401707 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9603,GWAS_ID_9604,GWAS_ID_9605 81543 RMVar_ID_81543 Human_SNP_ID_657956743 m1A Human chr19 + 9621174 9621174 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGCTGACTCCACCACCATAAAGGCGAAACCGCACTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs10401707 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9603,GWAS_ID_9604,GWAS_ID_9605 81544 RMVar_ID_81544 Human_SNP_ID_657956925 m1A Human chr19 - 9621588 9621588 9621588 ACAGGCGTGAGCCACTGCGCTCGCCCGATAAAAGCTTTGGAGGAGCATCCCCCGGGGATGCGTCC ACAGGCGTGAGCCACTGCGCTCGCCCGATAAATGCTTTGGAGGAGCATCCCCCGGGGATGCGTCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:9621543..9621627 26863196 MeRIP-seq:(Medium) rs1236959984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227 81545 RMVar_ID_81545 Human_SNP_ID_657962102 m1A Human chr19 + 9640772 9640769 9640772 AGCGTTATAGGGTGGGGTAGCAGAGGCTGCAGAAGAATTGGGACCCAATTCAGCCTGGCGAGGAG AGCGTTATAGGGTGGGGTAGCAGAGGCTGC___AGAATTGGGACCCAATTCAGCCTGGCGAGGAG CAGA C ZNF561-AS1 Ensembl:ENSG00000267106 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9640726..9640946 26863196 MeRIP-seq:(Medium) rs1424322288 Functional Loss DEL dbSNP153 31..33 33 - - - 81546 RMVar_ID_81546 Human_SNP_ID_657962116 m1A Human chr19 - 9640809 9640809 9640809 ACTGACCCCTCTGACCTCTCTCCTCCTCCCCCAGCTGCTCCTCGCCAGGCTGAATTGGGTCCCAA ACTGACCCCTCTGACCTCTCTCCTCCTCCCCCGGCTGCTCCTCGCCAGGCTGAATTGGGTCCCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:9640676..9640906 26863196 MeRIP-seq:(Medium) rs1369531655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227 81547 RMVar_ID_81547 Human_SNP_ID_657971883 m1A Human chr19 - 9673010 9673010 9673010 AGGTTGTTTACAGTAACTAGAGGCAAGGAGGCATGGAGAACAGGAAAGTTGAGTTTGAGAACAAA AGGTTGTTTACAGTAACTAGAGGCAAGGAGGCCTGGAGAACAGGAAAGTTGAGTTTGAGAACAAA T G ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:9672998..9673082 26863196 MeRIP-seq:(Medium) rs762430926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13541974 RMVar_hsa_circ_192227 81548 RMVar_ID_81548 Human_SNP_ID_658004213 m1A Human chr19 + 9768567 9768567 9768567 CTGGCGGGGAGGAGGCGCCGCTTCTCCGGAGCAGCAGCGGGAGGCCGGCGCGTCTCAGACCTAGC CTGGCGGGGAGGAGGCGCCGCTTCTCCGGAGCGGCAGCGGGAGGCCGGCGCGTCTCAGACCTAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:9768418..9768616 26863196 MeRIP-seq:(Medium) rs1433188944 Functional Loss SNV dbSNP153 33..33 33 - - - 81549 RMVar_ID_81549 Human_SNP_ID_658017892 m1A Human chr19 + 9819026 9819026 9819026 ACCAGCCTGGAAAGCGTGGCTGAGGCAGTGAGAGGCTTGCGGGAGGTGGCTGAGGCGTGATTTGG ACCAGCCTGGAAAGCGTGGCTGAGGCAGTGAGCGGCTTGCGGGAGGTGGCTGAGGCGTGATTTGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9818977..9819289 26863196 MeRIP-seq:(Medium) rs980773023 Functional Loss SNV dbSNP153 33..33 33 - - - 81550 RMVar_ID_81550 Human_SNP_ID_658018094 m1A Human chr19 + 9819478 9819478 9819478 CAGAAGGCGTGGCTGGGGTGGGGCGAGGATCAAGCCCGGAAGGCGCGGCTGGAGCGGGGCGAGGC CAGAAGGCGTGGCTGGGGTGGGGCGAGGATCACGCCCGGAAGGCGCGGCTGGAGCGGGGCGAGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:9819434..9819573 26863196 MeRIP-seq:(Medium) rs1289846253 Functional Loss SNV dbSNP153 33..33 33 - - - 81551 RMVar_ID_81551 Human_SNP_ID_658018343 m1A Human chr19 - 9820430 9820430 9820430 GCCCTCATGAGTGCAGGGCCAGCCACTTGTCCAGAGGGCCACGATTGGGGATGTACTTGACCCCA GCCCTCATGAGTGCAGGGCCAGCCACTTGTCCGGAGGGCCACGATTGGGGATGTACTTGACCCCA T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:9820339..9820430 32194978 MeRIP-seq:(Medium) rs1259909106 Functional Loss SNV dbSNP153 33..33 33 - - - 81552 RMVar_ID_81552 Human_SNP_ID_658020484 m1A Human chr19 + 9827978 9827978 9827978 GAGGAGCTGGTGGCGTCGGCAGGTTCGAGGCGATTCGAGGTGAGGGGGTCAAGCGGAGAGGCTCG GAGGAGCTGGTGGCGTCGGCAGGTTCGAGGCGGTTCGAGGTGAGGGGGTCAAGCGGAGAGGCTCG A G UBL5 Ensembl:ENSG00000198258 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:9827901..9828475;chr19:9827901..9828600 26863196 MeRIP-seq:(Medium) rs1465028735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240802,Human_RBP_ID_825235,Human_RBP_ID_907264,Human_RBP_ID_4557200,Human_RBP_ID_5116645,Human_RBP_ID_5144996,Human_RBP_ID_5320134,Human_RBP_ID_9328563,Human_RBP_ID_17655914,Human_RBP_ID_18421545,Human_RBP_ID_19089141,Human_RBP_ID_22446390 Human_Splice_Rec_1952565,Human_Splice_Rec_1952573,Human_Splice_Rec_1952589,Human_Splice_Rec_1952593,Human_Splice_Rec_1952597,Human_Splice_Rec_1952599,Human_Splice_Rec_1952603 Human_miRNA_ID_2660570,Human_miRNA_ID_2660571 RMVar_hsa_circ_119094,RMVar_hsa_circ_90646,RMVar_hsa_circ_192244,RMVar_hsa_circ_192245 81553 RMVar_ID_81553 Human_SNP_ID_658020485 m1A Human chr19 - 9827979 9827979 9827979 CCGAGCCTCTCCGCTTGACCCCCTCACCTCGAATCGCCTCGAACCTGCCGACGCCACCAGCTCCT CCGAGCCTCTCCGCTTGACCCCCTCACCTCGAGTCGCCTCGAACCTGCCGACGCCACCAGCTCCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:9827926..9828000 26863196 MeRIP-seq:(Medium) rs1307387287 Functional Loss SNV dbSNP153 33..33 33 - - - 81554 RMVar_ID_81554 Human_SNP_ID_658020679 m1A Human chr19 - 9828578 9828578 9828578 CCCGATGGTATCATCCGTGCTGGGCGCAGAGCAGTTAAGGCAAATGGAAGCGGTAGAACGAGGAA CCCGATGGTATCATCCGTGCTGGGCGCAGAGCGGTTAAGGCAAATGGAAGCGGTAGAACGAGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:9828576..9828625 26863196 MeRIP-seq:(Medium) rs780886277 Functional Loss SNV dbSNP153 33..33 33 - - - 81555 RMVar_ID_81555 Human_SNP_ID_658023411 m1A Human chr19 + 9838381 9838380 9838381 AGGCCCTCACCCTGGCTTCTGGCTGTGGGCCCAGGGGTGTCCTGGGAGCACAACCCTAGCTGAAT AGGCCCTCACCCTGGCTTCTGGCTGTGGGCCC_GGGGTGTCCTGGGAGCACAACCCTAGCTGAAT CA C PIN1 Ensembl:ENSG00000127445 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:9838373..9838455 26863410 MeRIP-seq:(Medium) rs1477115196 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22545558,Human_RBP_ID_22664762 RMVar_hsa_circ_358349 81556 RMVar_ID_81556 Human_SNP_ID_658023498 m1A Human chr19 + 9838568 9838568 9838568 CAGGGTCCGCTGCTCGCACCTGCTGGTGAAGCACAGCCAGTCACGGCGGCCCTCGTCCTGGCGGC CAGGGTCCGCTGCTCGCACCTGCTGGTGAAGCCCAGCCAGTCACGGCGGCCCTCGTCCTGGCGGC A C PIN1 Ensembl:ENSG00000127445 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9838388..9838650 26863196 MeRIP-seq:(Medium) rs79067653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530271,Human_RBP_ID_4556868,Human_RBP_ID_9381887,Human_RBP_ID_17934852,Human_RBP_ID_22446397,Human_RBP_ID_26815207 Human_Splice_Rec_1952615,Human_Splice_Rec_1952621,Human_Splice_Rec_1952623,Human_Splice_Rec_1952631,Human_Splice_Rec_1952639,Human_Splice_Rec_1952649,Human_Splice_Rec_1952659,Human_Splice_Rec_1952667,Human_Splice_Rec_1952675,Human_Splice_Rec_1952681 Human_miRNA_ID_2037971,Human_miRNA_ID_2237755,Human_miRNA_ID_2333239,Human_miRNA_ID_2348671,Human_miRNA_ID_2966322 RMVar_hsa_circ_73570,RMVar_hsa_circ_358349,RMVar_hsa_circ_108096,RMVar_hsa_circ_372365,RMVar_hsa_circ_192251,RMVar_hsa_circ_192252 81557 RMVar_ID_81557 Human_SNP_ID_658025887 m1A Human chr19 + 9848044 9848044 9848044 TCCGTTCCATGTCCACAGGCTACATCCAGAAGATCAAGTCGGGAGAGGAGGACTTTGAGTCTCTG TCCGTTCCATGTCCACAGGCTACATCCAGAAGGTCAAGTCGGGAGAGGAGGACTTTGAGTCTCTG A G PIN1 Ensembl:ENSG00000127445 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:9848026..9848125 26863196 MeRIP-seq:(Medium) rs767555744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575188,Human_RBP_ID_4575249,Human_RBP_ID_5116650,Human_RBP_ID_5190878,Human_RBP_ID_6796670,Human_RBP_ID_17934723,Human_RBP_ID_19092062,Human_RBP_ID_22661982 Human_Splice_Rec_1952616,Human_Splice_Rec_1952617,Human_Splice_Rec_1952622,Human_Splice_Rec_1952624,Human_Splice_Rec_1952625,Human_Splice_Rec_1952632,Human_Splice_Rec_1952633,Human_Splice_Rec_1952640,Human_Splice_Rec_1952641,Human_Splice_Rec_1952650,Human_Splice_Rec_1952651,Human_Splice_Rec_1952660,Human_Splice_Rec_1952661,Human_Splice_Rec_1952668,Human_Splice_Rec_1952669,Human_Splice_Rec_1952676,Human_Splice_Rec_1952677,Human_Splice_Rec_1952682,Human_Splice_Rec_1952683 RMVar_hsa_circ_73570,RMVar_hsa_circ_108096,RMVar_hsa_circ_192252 81558 RMVar_ID_81558 Human_SNP_ID_658026178 m1A Human chr19 + 9849106 9849106 9849106 CCCTCCTGGCTCCCAGGTCAGATGCAGAAGCCATTTGAAGACGCCTCGTTTGCGCTGCGGACGGG CCCTCCTGGCTCCCAGGTCAGATGCAGAAGCCGTTTGAAGACGCCTCGTTTGCGCTGCGGACGGG A G PIN1 Ensembl:ENSG00000127445 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:9849086..9849282 26863196 MeRIP-seq:(Medium) rs11540415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1192311,Human_RBP_ID_4575252,Human_RBP_ID_22813113 Human_Splice_Rec_1952618,Human_Splice_Rec_1952626,Human_Splice_Rec_1952634,Human_Splice_Rec_1952635,Human_Splice_Rec_1952642,Human_Splice_Rec_1952643,Human_Splice_Rec_1952652,Human_Splice_Rec_1952662,Human_Splice_Rec_1952670,Human_Splice_Rec_1952678,Human_Splice_Rec_1952679,Human_Splice_Rec_1952684 RMVar_hsa_circ_108096,RMVar_hsa_circ_192252,RMVar_hsa_circ_268543 81559 RMVar_ID_81559 Human_SNP_ID_658026232 m1A Human chr19 + 9849230 9849225 9849230 GAGGGTGGGGAGCCCAGGCCTGGCCTCGGGGCAGGGCAGGGCGGCTAGGCCGGCCAGCTCCCCCT GAGGGTGGGGAGCCCAGGCCTGGCCTCG_____GGGCAGGGCGGCTAGGCCGGCCAGCTCCCCCT GGGGCA G PIN1 Ensembl:ENSG00000127445 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:9849126..9849325 26863410 MeRIP-seq:(Medium) rs781615417 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_530275,Human_RBP_ID_1019478,Human_RBP_ID_17656722,Human_RBP_ID_22447358 Human_Splice_Rec_1952685 Human_miRNA_ID_3010973 RMVar_hsa_circ_108096,RMVar_hsa_circ_192252,RMVar_hsa_circ_268543 81560 RMVar_ID_81560 Human_SNP_ID_658026390 m1A Human chr19 + 9849558 9849558 9849558 CCCCCAGGTGCTGGAGGCAGACTCGAGGGCCGAATTGTTTCTAGTTAGGCCACGCTCCTCTGTTC CCCCCAGGTGCTGGAGGCAGACTCGAGGGCCGGATTGTTTCTAGTTAGGCCACGCTCCTCTGTTC A G PIN1 Ensembl:ENSG00000127445 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:9848560..9849700 32194978 MeRIP-seq:(Medium) rs558957674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530283,Human_RBP_ID_771363,Human_RBP_ID_1894155,Human_RBP_ID_3579607,Human_RBP_ID_5116652,Human_RBP_ID_6796676,Human_RBP_ID_13542662,Human_RBP_ID_17934729,Human_RBP_ID_18165632,Human_RBP_ID_18742843,Human_RBP_ID_26471955,Human_RBP_ID_26815208 Human_Splice_Rec_1952636,Human_Splice_Rec_1952644,Human_Splice_Rec_1952680,Human_Splice_Rec_1952686 RMVar_hsa_circ_108096,RMVar_hsa_circ_192252,RMVar_hsa_circ_268543 81561 RMVar_ID_81561 Human_SNP_ID_658093426 m1A Human chr19 + 10086383 10086383 10086383 CCGACGGGCGCACCCAGGTAGGGGGGCGGCTGAGCCGCGCAGTGCGGACCCTCGCGGGGAACTGC CCGACGGGCGCACCCAGGTAGGGGGGCGGCTGGGCCGCGCAGTGCGGACCCTCGCGGGGAACTGC A G SHFL Ensembl:ENSG00000130813 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10086152..10086478 26863196 MeRIP-seq:(Medium) rs1188059071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773929,Human_RBP_ID_4558028 Human_Splice_Rec_1953001,Human_Splice_Rec_1953005,Human_Splice_Rec_1953017,Human_Splice_Rec_1953031,Human_Splice_Rec_1953045 81562 RMVar_ID_81562 Human_SNP_ID_658093431 m1A Human chr19 + 10086391 10086391 10086391 CGCACCCAGGTAGGGGGGCGGCTGAGCCGCGCAGTGCGGACCCTCGCGGGGAACTGCGCCGCCGC CGCACCCAGGTAGGGGGGCGGCTGAGCCGCGCGGTGCGGACCCTCGCGGGGAACTGCGCCGCCGC A G SHFL Ensembl:ENSG00000130813 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10086146..10087349 26863196 MeRIP-seq:(Medium) rs1463984251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558028 Human_Splice_Rec_1953001,Human_Splice_Rec_1953005,Human_Splice_Rec_1953017,Human_Splice_Rec_1953031,Human_Splice_Rec_1953045 81563 RMVar_ID_81563 Human_SNP_ID_658093675 m1A Human chr19 - 10087044 10087044 10087044 GGCCCGGGACCCCTGCAGCCTCACCGTACACGATGGAGCGCCCCACTCCCGTGTGGTCGCTGCCG GGCCCGGGACCCCTGCAGCCTCACCGTACACGGTGGAGCGCCCCACTCCCGTGTGGTCGCTGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10086905..10087050 26863196 MeRIP-seq:(Medium) rs1403356644 Functional Loss SNV dbSNP153 33..33 33 - - - 81564 RMVar_ID_81564 Human_SNP_ID_658099931 m1A Human chr19 - 10106414 10106414 10106414 TGCGCCACCTGCCTCCCAAGCTGCCGGGCCTTACCCTCCCTGACTGTCCCATGCTGCTGTGTCCT TGCGCCACCTGCCTCCCAAGCTGCCGGGCCTTCCCCTCCCTGACTGTCCCATGCTGCTGTGTCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:10106385..10106596;chr19:10106389..10106569 26863196 MeRIP-seq:(Medium) rs948878951 Functional Loss SNV dbSNP153 33..33 33 - - - 81565 RMVar_ID_81565 Human_SNP_ID_658100421 m1A Human chr19 - 10107575 10107574 10107575 CAAAGTAGACATTGGTCTCTGTTTTGCTCAGGATCAGAAAGTGTGTGACCCCGAGGGGCCCAGCC CAAAGTAGACATTGGTCTCTGTTTTGCTCAGG_TCAGAAAGTGTGTGACCCCGAGGGGCCCAGCC AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10107526..10107637 26863196 MeRIP-seq:(Medium) rs1338329997 Functional Loss DEL dbSNP153 33..33 33 - - - 81566 RMVar_ID_81566 Human_SNP_ID_658100691 m1A Human chr19 + 10108051 10108051 10108051 AGCAGTTTGCCCACCCACCCCTCCTGGTACTCAACAGCTTTGGCCCCCATGGTATGCATGTGAAG AGCAGTTTGCCCACCCACCCCTCCTGGTACTCTACAGCTTTGGCCCCCATGGTATGCATGTGAAG A T PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10108001..10108169 26863196 MeRIP-seq:(Medium) rs1004131383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18440372,Human_RBP_ID_18720967,Human_RBP_ID_23780551 Human_Splice_Rec_1953140,Human_Splice_Rec_1953141,Human_Splice_Rec_1953162,Human_Splice_Rec_1953163,Human_Splice_Rec_1953184,Human_Splice_Rec_1953185,Human_Splice_Rec_1953204,Human_Splice_Rec_1953205,Human_Splice_Rec_1953226,Human_Splice_Rec_1953227,Human_Splice_Rec_1953238,Human_Splice_Rec_1953239 Human_miRNA_ID_2150182,Human_miRNA_ID_2407456,Human_miRNA_ID_2410451,Human_miRNA_ID_2413431,Human_miRNA_ID_2416403,Human_miRNA_ID_2624916 RMVar_hsa_circ_82075,RMVar_hsa_circ_192259,RMVar_hsa_circ_304501,RMVar_hsa_circ_77059,RMVar_hsa_circ_192260,RMVar_hsa_circ_192261 81567 RMVar_ID_81567 Human_SNP_ID_658101881 m1A Human chr19 + 10110704 10110704 10110704 TGTTGACCCCCACGCCCTCCTCCAGAAAGAAGAGCCTGGAGGGCATGAAGAAGGCACGGGTCGGG TGTTGACCCCCACGCCCTCCTCCAGAAAGAAGTGCCTGGAGGGCATGAAGAAGGCACGGGTCGGG A T PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10110501..10113647 26863196 MeRIP-seq:(Medium) rs1305242706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369916,Human_RBP_ID_8255739,Human_RBP_ID_18996431,Human_RBP_ID_22742403,Human_RBP_ID_26337285 Human_Splice_Rec_1953152,Human_Splice_Rec_1953174,Human_Splice_Rec_1953196,Human_Splice_Rec_1953216,Human_Splice_Rec_1953250,Human_Splice_Rec_1953256,Human_Splice_Rec_1953257,Human_Splice_Rec_1953260 RMVar_hsa_circ_68725,RMVar_hsa_circ_51209 81568 RMVar_ID_81568 Human_SNP_ID_658101899 m1A Human chr19 + 10110719 10110719 10110719 CCTCCTCCAGAAAGAAGAGCCTGGAGGGCATGAAGAAGGCACGGGTCGGGGGTAGTGATGAAGAG CCTCCTCCAGAAAGAAGAGCCTGGAGGGCATGGAGAAGGCACGGGTCGGGGGTAGTGATGAAGAG A G PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10110326..10113696 26863196 MeRIP-seq:(Medium) rs1327707707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6716490,Human_RBP_ID_8255739,Human_RBP_ID_22742403,Human_RBP_ID_26337285 Human_Splice_Rec_1953152,Human_Splice_Rec_1953174,Human_Splice_Rec_1953196,Human_Splice_Rec_1953216,Human_Splice_Rec_1953250,Human_Splice_Rec_1953256,Human_Splice_Rec_1953257,Human_Splice_Rec_1953260 RMVar_hsa_circ_68725,RMVar_hsa_circ_51209 81569 RMVar_ID_81569 Human_SNP_ID_658101944 m1A Human chr19 - 10110783 10110783 10110783 CTTCCTGTTCATCATCGTCCTCACCCAACTCCAGGCTCGCCGTCCTTGAAGGGATCCCAGAGGCC CTTCCTGTTCATCATCGTCCTCACCCAACTCCGGGCTCGCCGTCCTTGAAGGGATCCCAGAGGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:10110724..10113696;chr19:10109666..10113876 32194978 MeRIP-seq:(Medium) rs1472499755 Functional Loss SNV dbSNP153 33..33 33 - - - 81570 RMVar_ID_81570 Human_SNP_ID_658102394 m1A Human chr19 - 10111723 10111723 10111723 ATGCCTTCTCCTTACCCGAGACGTTGGCTGCCATGCTCCCGTGCCGATCCTCAGCCTGTGTCTGC ATGCCTTCTCCTTACCCGAGACGTTGGCTGCCGTGCTCCCGTGCCGATCCTCAGCCTGTGTCTGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:10111621..10111798 26863196 MeRIP-seq:(Medium) rs1461864845 Functional Loss SNV dbSNP153 33..33 33 - - - 81571 RMVar_ID_81571 Human_SNP_ID_658102753 m1A Human chr19 + 10112576 10112576 10112576 AAGGGAGAGTGGAGGCACGAGGGCTGCTGTCAACAGTGGTTAGGGTGGCCTTGGGGCCTCTCGCA AAGGGAGAGTGGAGGCACGAGGGCTGCTGTCAGCAGTGGTTAGGGTGGCCTTGGGGCCTCTCGCA A G PPAN-P2RY11,P2RY11 Ensembl:ENSG00000243207,Ensembl:ENSG00000244165 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10112388..10112777 26863196 MeRIP-seq:(Medium) rs911646965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263807,Human_RBP_ID_1553110,Human_RBP_ID_3583175,Human_RBP_ID_8100330,Human_RBP_ID_9428084,Human_RBP_ID_13355111,Human_RBP_ID_24552807,Human_RBP_ID_26337292,Human_RBP_ID_26473442 RMVar_hsa_circ_105573,RMVar_hsa_circ_192264 81572 RMVar_ID_81572 Human_SNP_ID_658103956 m1A Human chr19 - 10114684 10114684 10114684 TGGGGCTCTGACGGTTTAGGGGCGGCTGTGGCATTGAGGGGCAGGGCTTGGCCAGTGCTCTTGGC TGGGGCTCTGACGGTTTAGGGGCGGCTGTGGCGTTGAGGGGCAGGGCTTGGCCAGTGCTCTTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10114635..10114882 26863196 MeRIP-seq:(Medium) rs750097274 Functional Loss SNV dbSNP153 33..33 33 - - - 81573 RMVar_ID_81573 Human_SNP_ID_658104011 m1A Human chr19 - 10114763 10114761 10114763 GCCCTCAGGGTTCTCCAGCAACACCTAGGGTGAGGAGGCAGCTTCCGCTAGGCCACATCATTGGC GCCCTCAGGGTTCTCCAGCAACACCTAGGGTG__GAGGCAGCTTCCGCTAGGCCACATCATTGGC CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10114723..10114823 32194978 MeRIP-seq:(Medium) rs752971601 Functional Loss DEL dbSNP153 33..34 33 - - - 81574 RMVar_ID_81574 Human_SNP_ID_658104218 m1A Human chr19 - 10115110 10115110 10115110 TCCCCTACCCCAGGCCGTCCACCAACTAAGCCAGCTGCCACTGTGTACTCGGTCCGGGACCCTTG TCCCCTACCCCAGGCCGTCCACCAACTAAGCCGGCTGCCACTGTGTACTCGGTCCGGGACCCTTG T C EIF3G Ensembl:ENSG00000130811 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10115061..10115197 26863196 MeRIP-seq:(Medium) rs373177628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54045,Human_RBP_ID_511914,Human_RBP_ID_1553169,Human_RBP_ID_4560675,Human_RBP_ID_17082933,Human_RBP_ID_17655924,Human_RBP_ID_18165946,Human_RBP_ID_18191930,Human_RBP_ID_18721069,Human_RBP_ID_22449200,Human_RBP_ID_24552926,Human_RBP_ID_26816917 Human_Splice_Rec_1953286,Human_Splice_Rec_1953294,Human_Splice_Rec_1953300 Human_miRNA_ID_161560,Human_miRNA_ID_1996858,Human_miRNA_ID_2229351,Human_miRNA_ID_2505321 RMVar_hsa_circ_102942,RMVar_hsa_circ_124534,RMVar_hsa_circ_192266,RMVar_hsa_circ_87997,RMVar_hsa_circ_192267,RMVar_hsa_circ_192265 81575 RMVar_ID_81575 Human_SNP_ID_658104542 m1A Human chr19 - 10115811 10115809 10115812 GCCACCTCCCCTCTCCCACACAGCCGACGACAACGCCACCATCCGTGTCACCAACTTGTCAGAGG GCCACCTCCCCTCTCCCACACAGCCGACGAC___GCCACCATCCGTGTCACCAACTTGTCAGAGG CGTT C EIF3G Ensembl:ENSG00000130811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:10115667..10115852;chr19:10115804..10115930 26863196 MeRIP-seq:(Medium) rs758688972 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_240288,Human_RBP_ID_5421096,Human_RBP_ID_18192850,Human_RBP_ID_26815217 Human_Splice_Rec_1953282,Human_Splice_Rec_1953296,Human_Splice_Rec_1953314,Human_Splice_Rec_1953330,Human_Splice_Rec_1953346 Human_miRNA_ID_1957681 RMVar_hsa_circ_102942,RMVar_hsa_circ_124534,RMVar_hsa_circ_192266,RMVar_hsa_circ_87997,RMVar_hsa_circ_192267,RMVar_hsa_circ_192265,RMVar_hsa_circ_192268 81576 RMVar_ID_81576 Human_SNP_ID_658104545 m1A Human chr19 - 10115811 10115811 10115811 GCCACCTCCCCTCTCCCACACAGCCGACGACAACGCCACCATCCGTGTCACCAACTTGTCAGAGG GCCACCTCCCCTCTCCCACACAGCCGACGACAGCGCCACCATCCGTGTCACCAACTTGTCAGAGG T C EIF3G Ensembl:ENSG00000130811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:10115667..10115852;chr19:10115804..10115930 26863196 MeRIP-seq:(Medium) rs1440200016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240288,Human_RBP_ID_5421096,Human_RBP_ID_18192850,Human_RBP_ID_26815217 Human_Splice_Rec_1953282,Human_Splice_Rec_1953296,Human_Splice_Rec_1953314,Human_Splice_Rec_1953330,Human_Splice_Rec_1953346 Human_miRNA_ID_1957681 RMVar_hsa_circ_102942,RMVar_hsa_circ_124534,RMVar_hsa_circ_192266,RMVar_hsa_circ_87997,RMVar_hsa_circ_192267,RMVar_hsa_circ_192265,RMVar_hsa_circ_192268 81577 RMVar_ID_81577 Human_SNP_ID_658105892 m1A Human chr19 - 10119160 10119160 10119160 TTCCTACGCTGCCTTTTGCAGACAAATGTGTCACCAGCGAGCTCCTCAAGGGGATCCCTCTGGCC TTCCTACGCTGCCTTTTGCAGACAAATGTGTCGCCAGCGAGCTCCTCAAGGGGATCCCTCTGGCC T C EIF3G Ensembl:ENSG00000130811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:10119050..10119211;chr19:10119048..10119201 26863196 MeRIP-seq:(Medium) rs1335207002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240295,Human_RBP_ID_771711,Human_RBP_ID_825880,Human_RBP_ID_914106,Human_RBP_ID_1553226,Human_RBP_ID_3954377,Human_RBP_ID_5468186,Human_RBP_ID_5498822,Human_RBP_ID_8475934,Human_RBP_ID_9380341,Human_RBP_ID_18421546,Human_RBP_ID_18996450,Human_RBP_ID_22069662,Human_RBP_ID_22448349,Human_RBP_ID_26816932,Human_RBP_ID_27462609 Human_Splice_Rec_1953270,Human_Splice_Rec_1953271,Human_Splice_Rec_1953304,Human_Splice_Rec_1953305,Human_Splice_Rec_1953320,Human_Splice_Rec_1953321,Human_Splice_Rec_1953334,Human_Splice_Rec_1953335,Human_Splice_Rec_1953350,Human_Splice_Rec_1953360,Human_Splice_Rec_1953361,Human_Splice_Rec_1953374,Human_Splice_Rec_1953375,Human_Splice_Rec_1953386,Human_Splice_Rec_1953387,Human_Splice_Rec_1953396,Human_Splice_Rec_1953397,Human_Splice_Rec_1953406,Human_Splice_Rec_1953407,Human_Splice_Rec_1953414,Human_Splice_Rec_1953415 RMVar_hsa_circ_102942,RMVar_hsa_circ_192265,RMVar_hsa_circ_192269,RMVar_hsa_circ_121731,RMVar_hsa_circ_373514,RMVar_hsa_circ_192270,RMVar_hsa_circ_39414 81578 RMVar_ID_81578 Human_SNP_ID_658106128 m1A Human chr19 - 10119695 10119695 10119695 TCGTTCCCCACACATTTGTTTCCGCAGTTCGAAGCCCAGTTGGGCCGACCAGGTGGAGGAGGAGG TCGTTCCCCACACATTTGTTTCCGCAGTTCGAGGCCCAGTTGGGCCGACCAGGTGGAGGAGGAGG T C EIF3G Ensembl:ENSG00000130811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10119651..10119725 26863196 MeRIP-seq:(Medium) rs1224573301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240296,Human_RBP_ID_771712,Human_RBP_ID_2555266,Human_RBP_ID_3956183,Human_RBP_ID_4558033,Human_RBP_ID_5116656,Human_RBP_ID_8255744,Human_RBP_ID_9380342,Human_RBP_ID_18470482,Human_RBP_ID_22449209,Human_RBP_ID_22808788,Human_RBP_ID_26335520 Human_Splice_Rec_1953268,Human_Splice_Rec_1953269,Human_Splice_Rec_1953302,Human_Splice_Rec_1953303,Human_Splice_Rec_1953318,Human_Splice_Rec_1953319,Human_Splice_Rec_1953332,Human_Splice_Rec_1953333,Human_Splice_Rec_1953348,Human_Splice_Rec_1953349,Human_Splice_Rec_1953358,Human_Splice_Rec_1953359,Human_Splice_Rec_1953372,Human_Splice_Rec_1953373,Human_Splice_Rec_1953384,Human_Splice_Rec_1953385,Human_Splice_Rec_1953395,Human_Splice_Rec_1953404,Human_Splice_Rec_1953405,Human_Splice_Rec_1953413,Human_Splice_Rec_1953418 Human_miRNA_ID_2555136 RMVar_hsa_circ_102942,RMVar_hsa_circ_192265,RMVar_hsa_circ_192269,RMVar_hsa_circ_121731,RMVar_hsa_circ_373514,RMVar_hsa_circ_192270,RMVar_hsa_circ_39414 81579 RMVar_ID_81579 Human_SNP_ID_658106178 m1A Human chr19 + 10119802 10119802 10119802 CCAGGCCCCATAATACTTCCCAGAGCACCCCAACCGCTTCCCGTGCCCCTTTCCGCGATCGCCGA CCAGGCCCCATAATACTTCCCAGAGCACCCCAGCCGCTTCCCGTGCCCCTTTCCGCGATCGCCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10119796..10119900 26863196 MeRIP-seq:(Medium) rs1157872830 Functional Loss SNV dbSNP153 33..33 33 - - - 81580 RMVar_ID_81580 Human_SNP_ID_658113029 m1A Human chr19 + 10143752 10143733 10143752 CTAGAAGAGTCTGTGGCCTCGTGGAAGAACAGAGGCCTCTGCTGACCTGTAGAACTTGTTGACCC CTAGAAGAGTCTGT___________________GGCCTCTGCTGACCTGTAGAACTTGTTGACCC TGGCCTCGTGGAAGAACAGA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10143751..10143775 32194978 MeRIP-seq:(Medium) rs1169365875 Functional Loss DEL dbSNP153 15..33 33 - - - 81581 RMVar_ID_81581 Human_SNP_ID_658113696 m1A Human chr19 + 10146297 10146297 10146297 AATGTCTGTAAGGAGGGGGACACCACAAAGCCAGCCTGGCTCAGCCTGGAGCGCCCTGGCCCCGG AATGTCTGTAAGGAGGGGGACACCACAAAGCCCGCCTGGCTCAGCCTGGAGCGCCCTGGCCCCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10146296..10146374 26863196 MeRIP-seq:(Medium) rs561684246 Functional Loss SNV dbSNP153 33..33 33 - - - 81582 RMVar_ID_81582 Human_SNP_ID_658116041 m1A Human chr19 - 10154451 10154451 10154451 GTAGGCGAGCCCAGGCGAGGCGGCAGACCATCAGGCATTCTACCAGGGAGAAGGACAGGGGACCC GTAGGCGAGCCCAGGCGAGGCGGCAGACCATCCGGCATTCTACCAGGGAGAAGGACAGGGGACCC T G DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10154401..10154675;chr19:10154401..10154475;chr19:10154357..10154700 26863196 MeRIP-seq:(Medium) rs144567470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8839040,Human_RBP_ID_9293319,Human_RBP_ID_18721201,Human_RBP_ID_22593307 Human_Splice_Rec_1953484,Human_Splice_Rec_1953564,Human_Splice_Rec_1953642,Human_Splice_Rec_1953744 Clinvar_Rec_383 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_103648,RMVar_hsa_circ_192276,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_118627,RMVar_hsa_circ_265839,RMVar_hsa_circ_192286,RMVar_hsa_circ_372162,RMVar_hsa_circ_35443,RMVar_hsa_circ_60396,RMVar_hsa_circ_105547,RMVar_hsa_circ_20992,RMVar_hsa_circ_62669,RMVar_hsa_circ_192290,RMVar_hsa_circ_192291,RMVar_hsa_circ_374471,RMVar_hsa_circ_377950,RMVar_hsa_circ_71818,RMVar_hsa_circ_294589,RMVar_hsa_circ_323728,RMVar_hsa_circ_272308,RMVar_hsa_circ_66651,RMVar_hsa_circ_68450,RMVar_hsa_circ_192293,RMVar_hsa_circ_62311,RMVar_hsa_circ_192294,RMVar_hsa_circ_192292,RMVar_hsa_circ_192297,RMVar_hsa_circ_18374,RMVar_hsa_circ_26817,RMVar_hsa_circ_275681,RMVar_hsa_circ_316491,RMVar_hsa_circ_322171,RMVar_hsa_circ_274885,RMVar_hsa_circ_192295,RMVar_hsa_circ_192296 81583 RMVar_ID_81583 Human_SNP_ID_658118530 m1A Human chr19 - 10163337 10163337 10163337 TTCTGTCAGGATGAGAAGAAGCACAGAAGTCAACCCAAAGATCTGTAAGTGTTTAAAATGCTTGT TTCTGTCAGGATGAGAAGAAGCACAGAAGTCAGCCCAAAGATCTGTAAGTGTTTAAAATGCTTGT T C DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10163326..10163375 26863196 MeRIP-seq:(Medium) rs368346471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908424,Human_RBP_ID_1553443,Human_RBP_ID_9346875,Human_RBP_ID_9380384,Human_RBP_ID_13356331,Human_RBP_ID_18412485,Human_RBP_ID_19089178,Human_RBP_ID_22662003,Human_RBP_ID_22808848,Human_RBP_ID_25440911,Human_RBP_ID_26337330,Human_RBP_ID_26981351,Human_RBP_ID_27816016 Human_Splice_Rec_1953464,Human_Splice_Rec_1953465,Human_Splice_Rec_1953544,Human_Splice_Rec_1953545,Human_Splice_Rec_1953622,Human_Splice_Rec_1953623,Human_Splice_Rec_1953764,Human_Splice_Rec_1953765,Human_Splice_Rec_1953772,Human_Splice_Rec_1953773 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_118627,RMVar_hsa_circ_265839,RMVar_hsa_circ_192286,RMVar_hsa_circ_35443,RMVar_hsa_circ_24852,RMVar_hsa_circ_105547,RMVar_hsa_circ_68450,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_126575,RMVar_hsa_circ_81880,RMVar_hsa_circ_192299,RMVar_hsa_circ_192300,RMVar_hsa_circ_192301,RMVar_hsa_circ_26729,RMVar_hsa_circ_317194,RMVar_hsa_circ_192307,RMVar_hsa_circ_350811,RMVar_hsa_circ_370530,RMVar_hsa_circ_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_346505,RMVar_hsa_circ_321726,RMVar_hsa_circ_61383,RMVar_hsa_circ_192309,RMVar_hsa_circ_192310,RMVar_hsa_circ_192308,RMVar_hsa_circ_308026,RMVar_hsa_circ_364236,RMVar_hsa_circ_47164,RMVar_hsa_circ_358923,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,RMVar_hsa_circ_59443,RMVar_hsa_circ_192311,RMVar_hsa_circ_192313,RMVar_hsa_circ_192314,RMVar_hsa_circ_192315,RMVar_hsa_circ_192312,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314 81584 RMVar_ID_81584 Human_SNP_ID_658118531 m1A Human chr19 - 10163337 10163337 10163337 TTCTGTCAGGATGAGAAGAAGCACAGAAGTCAACCCAAAGATCTGTAAGTGTTTAAAATGCTTGT TTCTGTCAGGATGAGAAGAAGCACAGAAGTCACCCCAAAGATCTGTAAGTGTTTAAAATGCTTGT T G DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10163326..10163375 26863196 MeRIP-seq:(Medium) rs368346471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908424,Human_RBP_ID_1553443,Human_RBP_ID_9346875,Human_RBP_ID_9380384,Human_RBP_ID_13356331,Human_RBP_ID_18412485,Human_RBP_ID_19089178,Human_RBP_ID_22662003,Human_RBP_ID_22808848,Human_RBP_ID_25440911,Human_RBP_ID_26337330,Human_RBP_ID_26981351,Human_RBP_ID_27816016 Human_Splice_Rec_1953464,Human_Splice_Rec_1953465,Human_Splice_Rec_1953544,Human_Splice_Rec_1953545,Human_Splice_Rec_1953622,Human_Splice_Rec_1953623,Human_Splice_Rec_1953764,Human_Splice_Rec_1953765,Human_Splice_Rec_1953772,Human_Splice_Rec_1953773 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_118627,RMVar_hsa_circ_265839,RMVar_hsa_circ_192286,RMVar_hsa_circ_35443,RMVar_hsa_circ_24852,RMVar_hsa_circ_105547,RMVar_hsa_circ_68450,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_126575,RMVar_hsa_circ_81880,RMVar_hsa_circ_192299,RMVar_hsa_circ_192300,RMVar_hsa_circ_192301,RMVar_hsa_circ_26729,RMVar_hsa_circ_317194,RMVar_hsa_circ_192307,RMVar_hsa_circ_350811,RMVar_hsa_circ_370530,RMVar_hsa_circ_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_346505,RMVar_hsa_circ_321726,RMVar_hsa_circ_61383,RMVar_hsa_circ_192309,RMVar_hsa_circ_192310,RMVar_hsa_circ_192308,RMVar_hsa_circ_308026,RMVar_hsa_circ_364236,RMVar_hsa_circ_47164,RMVar_hsa_circ_358923,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,RMVar_hsa_circ_59443,RMVar_hsa_circ_192311,RMVar_hsa_circ_192313,RMVar_hsa_circ_192314,RMVar_hsa_circ_192315,RMVar_hsa_circ_192312,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314 81585 RMVar_ID_81585 Human_SNP_ID_658119415 m1A Human chr19 - 10166617 10166617 10166617 AGAAGCCAGGGCAGGCGTGCAGGCTGACGAGGACGAAGATGGAGACGAGAAAGTAAAGGCGGGTT AGAAGCCAGGGCAGGCGTGCAGGCTGACGAGGCCGAAGATGGAGACGAGAAAGTAAAGGCGGGTT T G DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10163326..10173151 32194978 MeRIP-seq:(Medium) rs1169597458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54123,Human_RBP_ID_240315,Human_RBP_ID_825349,Human_RBP_ID_5588291,Human_RBP_ID_6716778,Human_RBP_ID_9380385,Human_RBP_ID_13356448,Human_RBP_ID_18440403,Human_RBP_ID_19092112,Human_RBP_ID_22978024,Human_RBP_ID_24545419,Human_RBP_ID_26335570,Human_RBP_ID_27815075 Human_Splice_Rec_1953462,Human_Splice_Rec_1953463,Human_Splice_Rec_1953542,Human_Splice_Rec_1953543,Human_Splice_Rec_1953620,Human_Splice_Rec_1953621,Human_Splice_Rec_1953763,Human_Splice_Rec_1953771 Human_miRNA_ID_1192064,Human_miRNA_ID_1541079,Human_miRNA_ID_1594617 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_265839,RMVar_hsa_circ_35443,RMVar_hsa_circ_24852,RMVar_hsa_circ_105547,RMVar_hsa_circ_68450,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_126575,RMVar_hsa_circ_81880,RMVar_hsa_circ_192299,RMVar_hsa_circ_192300,RMVar_hsa_circ_192301,RMVar_hsa_circ_26729,RMVar_hsa_circ_350811,RMVar_hsa_circ_370530,RMVar_hsa_circ_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_346505,RMVar_hsa_circ_61383,RMVar_hsa_circ_192309,RMVar_hsa_circ_192310,RMVar_hsa_circ_192308,RMVar_hsa_circ_308026,RMVar_hsa_circ_364236,RMVar_hsa_circ_47164,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,RMVar_hsa_circ_59443,RMVar_hsa_circ_192311,RMVar_hsa_circ_192313,RMVar_hsa_circ_192314,RMVar_hsa_circ_192312,RMVar_hsa_circ_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 81586 RMVar_ID_81586 Human_SNP_ID_658119421 m1A Human chr19 + 10166632 10166632 10166632 TCTCGTCTCCATCTTCGTCCTCGTCAGCCTGCACGCCTGCCCTGGCTTCTCTGTCCGGCTCCTCC TCTCGTCTCCATCTTCGTCCTCGTCAGCCTGCGCGCCTGCCCTGGCTTCTCTGTCCGGCTCCTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10163344..10166700 32194978 MeRIP-seq:(Medium) rs766504703 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_384 81587 RMVar_ID_81587 Human_SNP_ID_658119428 m1A Human chr19 - 10166651 10166651 10166651 CACCCAAACAGAAACTGAAGGAGGAGCCGGACAGAGAAGCCAGGGCAGGCGTGCAGGCTGACGAG CACCCAAACAGAAACTGAAGGAGGAGCCGGACGGAGAAGCCAGGGCAGGCGTGCAGGCTGACGAG T C DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:10166576..10166700 26863196 MeRIP-seq:(Medium) rs1419316960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54123,Human_RBP_ID_240315,Human_RBP_ID_913131,Human_RBP_ID_1553461,Human_RBP_ID_9380385,Human_RBP_ID_13356450,Human_RBP_ID_22978024,Human_RBP_ID_24545419,Human_RBP_ID_25380476,Human_RBP_ID_26334825,Human_RBP_ID_27815075 Human_Splice_Rec_1953462,Human_Splice_Rec_1953463,Human_Splice_Rec_1953542,Human_Splice_Rec_1953543,Human_Splice_Rec_1953620,Human_Splice_Rec_1953621,Human_Splice_Rec_1953763,Human_Splice_Rec_1953771 Human_miRNA_ID_3091244,Human_miRNA_ID_3118940 GWAS_ID_9606,GWAS_ID_9607 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_265839,RMVar_hsa_circ_35443,RMVar_hsa_circ_24852,RMVar_hsa_circ_105547,RMVar_hsa_circ_68450,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_126575,RMVar_hsa_circ_81880,RMVar_hsa_circ_192299,RMVar_hsa_circ_192300,RMVar_hsa_circ_192301,RMVar_hsa_circ_26729,RMVar_hsa_circ_350811,RMVar_hsa_circ_370530,RMVar_hsa_circ_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_346505,RMVar_hsa_circ_61383,RMVar_hsa_circ_192309,RMVar_hsa_circ_192310,RMVar_hsa_circ_192308,RMVar_hsa_circ_308026,RMVar_hsa_circ_364236,RMVar_hsa_circ_47164,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,RMVar_hsa_circ_59443,RMVar_hsa_circ_192311,RMVar_hsa_circ_192313,RMVar_hsa_circ_192314,RMVar_hsa_circ_192312,RMVar_hsa_circ_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 81588 RMVar_ID_81588 Human_SNP_ID_658119863 m1A Human chr19 - 10168332 10168332 10168332 GAAGAAAAGAGACTCCGAAGTCAAACCAAAGAACCGTAAGTGCAGCGAACCTGCCTTTGTGCTTT GAAGAAAAGAGACTCCGAAGTCAAACCAAAGAGCCGTAAGTGCAGCGAACCTGCCTTTGTGCTTT T C DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:10168326..10168375 26863196 MeRIP-seq:(Medium) rs1165073207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9346876,Human_RBP_ID_9380388,Human_RBP_ID_18721260,Human_RBP_ID_18996478,Human_RBP_ID_19089182,Human_RBP_ID_22664793,Human_RBP_ID_24545639,Human_RBP_ID_25380496,Human_RBP_ID_26335571 Human_Splice_Rec_1953460,Human_Splice_Rec_1953461,Human_Splice_Rec_1953540,Human_Splice_Rec_1953541,Human_Splice_Rec_1953618,Human_Splice_Rec_1953619,Human_Splice_Rec_1953796 RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_265839,RMVar_hsa_circ_35443,RMVar_hsa_circ_24852,RMVar_hsa_circ_105547,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_126575,RMVar_hsa_circ_81880,RMVar_hsa_circ_192299,RMVar_hsa_circ_192300,RMVar_hsa_circ_192301,RMVar_hsa_circ_26729,RMVar_hsa_circ_350811,RMVar_hsa_circ_370530,RMVar_hsa_circ_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_61383,RMVar_hsa_circ_192309,RMVar_hsa_circ_192310,RMVar_hsa_circ_364236,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,RMVar_hsa_circ_59443,RMVar_hsa_circ_192311,RMVar_hsa_circ_192313,RMVar_hsa_circ_192312,RMVar_hsa_circ_36419,RMVar_hsa_circ_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_319125,RMVar_hsa_circ_60933,RMVar_hsa_circ_268592,RMVar_hsa_circ_192317 81589 RMVar_ID_81589 Human_SNP_ID_658121154 m1A Human chr19 + 10173078 10173078 10173078 GGATTAAGGGAGAATTAACAAACTTAGAGGTGATAGAGCTTTACTTTTTCATCTCTTTCTTCTTC GGATTAAGGGAGAATTAACAAACTTAGAGGTGTTAGAGCTTTACTTTTTCATCTCTTTCTTCTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:10173076..10173175 26863196 MeRIP-seq:(Medium) rs189898346 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_385 81590 RMVar_ID_81590 Human_SNP_ID_658123245 m1A Human chr19 - 10180405 10180405 10180405 GTGGGAATGGCAGATGCCAACAGCCCCCCCAAACCCCTTTCCAAACCTCGCACGCCCAGGAGGAG GTGGGAATGGCAGATGCCAACAGCCCCCCCAAGCCCCTTTCCAAACCTCGCACGCCCAGGAGGAG T C DNMT1 Ensembl:ENSG00000130816 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10180318..10180472 26863196 MeRIP-seq:(Medium) rs373499917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771724,Human_RBP_ID_4497809,Human_RBP_ID_9380391,Human_RBP_ID_26335579 Human_Splice_Rec_1953449,Human_Splice_Rec_1953529,Human_Splice_Rec_1953609,Human_Splice_Rec_1953787,Human_Splice_Rec_1953805,Human_Splice_Rec_1953823,Human_Splice_Rec_1953833,Human_Splice_Rec_1953845,Human_Splice_Rec_1953849 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_126575,RMVar_hsa_circ_192300,RMVar_hsa_circ_61383,RMVar_hsa_circ_59709,RMVar_hsa_circ_6105,RMVar_hsa_circ_88665,RMVar_hsa_circ_192311,RMVar_hsa_circ_192312,RMVar_hsa_circ_363399,RMVar_hsa_circ_24650,RMVar_hsa_circ_121575,RMVar_hsa_circ_192320,RMVar_hsa_circ_41028,RMVar_hsa_circ_192323,RMVar_hsa_circ_326666,RMVar_hsa_circ_192324,RMVar_hsa_circ_298948,RMVar_hsa_circ_348487 81591 RMVar_ID_81591 Human_SNP_ID_658127310 m1A Human chr19 - 10194688 10194688 10194688 CGGGCGCGCATGCGTGGGGTGGTGCGGCGCGCAGCGGCAGTTGGCGCGGGCAGGGTGGCACTTCC CGGGCGCGCATGCGTGGGGTGGTGCGGCGCGCCGCGGCAGTTGGCGCGGGCAGGGTGGCACTTCC T G DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10194687..10194950 26863196 MeRIP-seq:(Medium) rs575808559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9353691,Human_RBP_ID_19094763 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 81592 RMVar_ID_81592 Human_SNP_ID_658127367 m1A Human chr19 + 10194809 10194809 10194809 CTGCCTGTCCCCCTGAGTCCGTGTTCCCCCCCATGGTACCTACCGCCTGCGGACATCGTCGGGCA CTGCCTGTCCCCCTGAGTCCGTGTTCCCCCCCCTGGTACCTACCGCCTGCGGACATCGTCGGGCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10194801..10194850 26863196 MeRIP-seq:(Medium) rs368945230 Functional Loss SNV dbSNP153 33..33 33 - - - 81593 RMVar_ID_81593 Human_SNP_ID_658127368 m1A Human chr19 + 10194809 10194809 10194809 CTGCCTGTCCCCCTGAGTCCGTGTTCCCCCCCATGGTACCTACCGCCTGCGGACATCGTCGGGCA CTGCCTGTCCCCCTGAGTCCGTGTTCCCCCCCGTGGTACCTACCGCCTGCGGACATCGTCGGGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10194801..10194850 26863196 MeRIP-seq:(Medium) rs368945230 Functional Loss SNV dbSNP153 33..33 33 - - - 81594 RMVar_ID_81594 Human_SNP_ID_658127423 m1A Human chr19 + 10194905 10194905 10194905 CCGGGCTGGGGCGGTACGCGCCGGCATCTCGGAGGCTTCAGCAGACGCGGCGGCGGCAGCGCAGG CCGGGCTGGGGCGGTACGCGCCGGCATCTCGGGGGCTTCAGCAGACGCGGCGGCGGCAGCGCAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:10194876..10194950;chr19:10194630..10194950;chr19:10194612..10194950;chr19:10194788..10194950 26863196 MeRIP-seq:(Medium) rs547079738 Functional Loss SNV dbSNP153 33..33 33 - - - 81595 RMVar_ID_81595 Human_SNP_ID_658145098 m1A Human chr19 - 10258524 10258524 10258524 GGCCCCCTGCCCCTGCTCTGCCCTGTGCCCTCACAAGTCCACGAGGAGTACGGAGTCCCCCCAGC GGCCCCCTGCCCCTGCTCTGCCCTGTGCCCTCGCAAGTCCACGAGGAGTACGGAGTCCCCCCAGC T C AC011511.2 Ensembl:ENSG00000266978 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10258397..10258560 26863196 MeRIP-seq:(Medium) rs780372999 Functional Loss SNV dbSNP153 33..33 33 - - - 81596 RMVar_ID_81596 Human_SNP_ID_658145099 m1A Human chr19 - 10258524 10258524 10258524 GGCCCCCTGCCCCTGCTCTGCCCTGTGCCCTCACAAGTCCACGAGGAGTACGGAGTCCCCCCAGC GGCCCCCTGCCCCTGCTCTGCCCTGTGCCCTCCCAAGTCCACGAGGAGTACGGAGTCCCCCCAGC T G AC011511.2 Ensembl:ENSG00000266978 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10258397..10258560 26863196 MeRIP-seq:(Medium) rs780372999 Functional Loss SNV dbSNP153 33..33 33 - - - 81597 RMVar_ID_81597 Human_SNP_ID_658145626 m1A Human chr19 + 10259748 10259748 10259748 ACAGACCCCTCTACCCCTTCAGCCTGCCCTACAGCGACTTCCCCCGACCCCTACCCCACGCTACC ACAGACCCCTCTACCCCTTCAGCCTGCCCTACGGCGACTTCCCCCGACCCCTACCCCACGCTACC A G MRPL4 Ensembl:ENSG00000105364 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10259697..10259896 32194978 MeRIP-seq:(Medium) rs770765591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241363,Human_RBP_ID_511997,Human_RBP_ID_5117679,Human_RBP_ID_8476093,Human_RBP_ID_17387199,Human_RBP_ID_17655926,Human_RBP_ID_18945022,Human_RBP_ID_27266754 81598 RMVar_ID_81598 Human_SNP_ID_658145652 m1A Human chr19 - 10259777 10259777 10259777 CAGTGGTACGGGGTGGCCGCTGGGCCCTGGGTAGCGTGGGGTAGGGGTCGGGGGAAGTCGCTGTA CAGTGGTACGGGGTGGCCGCTGGGCCCTGGGTGGCGTGGGGTAGGGGTCGGGGGAAGTCGCTGTA T C AC011511.2,AC011511.3 Ensembl:ENSG00000266978,Ensembl:ENSG00000267105 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:10259626..10259946;chr19:10259726..10259875 26863196 MeRIP-seq:(Medium) rs1195546337 Functional Loss SNV dbSNP153 33..33 33 - - - 81599 RMVar_ID_81599 Human_SNP_ID_658152787 m1A Human chr19 - 10284526 10284526 10284526 TGGCCTTCAGCAGGAGCTGGGCCCTCGGGCCCAGTGGCTGGGCTGGAACCCCATTCAGCGTCACC TGGCCTTCAGCAGGAGCTGGGCCCTCGGGCCCCGTGGCTGGGCTGGAACCCCATTCAGCGTCACC T G AC011511.2 Ensembl:ENSG00000266978 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10284476..10284576 32194978 MeRIP-seq:(Medium) rs983667097 Functional Loss SNV dbSNP153 33..33 33 - - - 81600 RMVar_ID_81600 Human_SNP_ID_658155311 m1A Human chr19 - 10292180 10292180 10292180 GCCACGAATGCGTCCCCTTCGAGGGTGACATCAGGACTCAGATTCTGGTCCCCCAGTGCGAGGTA GCCACGAATGCGTCCCCTTCGAGGGTGACATCGGGACTCAGATTCTGGTCCCCCAGTGCGAGGTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10292076..10292325 32194978 MeRIP-seq:(Medium) rs777499826 Functional Loss SNV dbSNP153 33..33 33 - - - 81601 RMVar_ID_81601 Human_SNP_ID_658155503 m1A Human chr19 - 10292720 10292720 10292720 GCTGGGCGGGCTGCCCCGGGACCGCGGCTGGAACTCCCTCCAGTGTGACCAGAGCTTGGGCCCCA GCTGGGCGGGCTGCCCCGGGACCGCGGCTGGAGCTCCCTCCAGTGTGACCAGAGCTTGGGCCCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10292601..10292775 32194978 MeRIP-seq:(Medium) rs1285195086 Functional Loss SNV dbSNP153 33..33 33 - - - 81602 RMVar_ID_81602 Human_SNP_ID_658155835 m1A Human chr19 - 10293746 10293746 10293746 CCACACAGCTCAGCGAGGCTTCTGTTCCCTCCAGCCAAGTAATGCGTTCTGGGCAGCCCACGCTG CCACACAGCTCAGCGAGGCTTCTGTTCCCTCCCGCCAAGTAATGCGTTCTGGGCAGCCCACGCTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10293726..10293750 32194978 MeRIP-seq:(Medium) rs750361196 Functional Loss SNV dbSNP153 33..33 33 - - - 81603 RMVar_ID_81603 Human_SNP_ID_658155969 m1A Human chr19 - 10294030 10294030 10294030 CGGCTCCTCAAACCTGGGGCCATCTGGGAAACAGGATTGCAGGGGCTCACACGGGGGCCAGGAAG CGGCTCCTCAAACCTGGGGCCATCTGGGAAACGGGATTGCAGGGGCTCACACGGGGGCCAGGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10294026..10294150 32194978 MeRIP-seq:(Medium) rs374601160 Functional Loss SNV dbSNP153 33..33 33 - - - 81604 RMVar_ID_81604 Human_SNP_ID_658156817 m1A Human chr19 - 10296660 10296660 10296660 AATAAATAAAGCAATAAATAAGCCCCCGTGTGAGTCTGGGGGGCGTCCCCCGGCCCGCGGGGAGA AATAAATAAAGCAATAAATAAGCCCCCGTGTGCGTCTGGGGGGCGTCCCCCGGCCCGCGGGGAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10296610..10296695 32194978 MeRIP-seq:(Medium) rs953416768 Functional Loss SNV dbSNP153 33..33 33 - - - 81605 RMVar_ID_81605 Human_SNP_ID_658161034 m1A Human chr19 - 10310456 10310456 10310456 TGACATGAACACCTGGACCATTCCACATTGCCATGGCCCCAGGGCCCAGATTGAGGGAATAGCCA TGACATGAACACCTGGACCATTCCACATTGCCTTGGCCCCAGGGCCCAGATTGAGGGAATAGCCA T A AC011511.1,FDX2 Ensembl:ENSG00000167807,Ensembl:ENSG00000267673 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10310405..10310591 26863196 MeRIP-seq:(Medium) rs773013930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553547,Human_RBP_ID_4560840,Human_RBP_ID_13357605,Human_RBP_ID_23780801 Human_Splice_Rec_1954129 Human_miRNA_ID_420860,Human_miRNA_ID_420861 81606 RMVar_ID_81606 Human_SNP_ID_658161035 m1A Human chr19 - 10310456 10310456 10310456 TGACATGAACACCTGGACCATTCCACATTGCCATGGCCCCAGGGCCCAGATTGAGGGAATAGCCA TGACATGAACACCTGGACCATTCCACATTGCCGTGGCCCCAGGGCCCAGATTGAGGGAATAGCCA T C AC011511.1,FDX2 Ensembl:ENSG00000167807,Ensembl:ENSG00000267673 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10310405..10310591 26863196 MeRIP-seq:(Medium) rs773013930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553547,Human_RBP_ID_4560840,Human_RBP_ID_13357605,Human_RBP_ID_23780801 Human_Splice_Rec_1954129 Human_miRNA_ID_420860,Human_miRNA_ID_420861 81607 RMVar_ID_81607 Human_SNP_ID_658162985 m1A Human chr19 - 10316395 10316395 10316395 CTCCATGAAGATAAACTCTGGGCCCGCCCACCAGCAGGACCTGTCGACCTGAGGTGACCCTGGGC CTCCATGAAGATAAACTCTGGGCCCGCCCACCTGCAGGACCTGTCGACCTGAGGTGACCCTGGGC T A RAVER1,AC011511.4 Ensembl:ENSG00000161847,Ensembl:ENSG00000267303 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10316344..10316417 26863196 MeRIP-seq:(Medium) rs969404676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512059,Human_RBP_ID_5190458,Human_RBP_ID_13357610,Human_RBP_ID_17272025,Human_RBP_ID_17386657,Human_RBP_ID_17914158,Human_RBP_ID_27266771 Human_miRNA_ID_272415,Human_miRNA_ID_272416,Human_miRNA_ID_1093897,Human_miRNA_ID_1093898 81608 RMVar_ID_81608 Human_SNP_ID_658162986 m1A Human chr19 - 10316395 10316395 10316395 CTCCATGAAGATAAACTCTGGGCCCGCCCACCAGCAGGACCTGTCGACCTGAGGTGACCCTGGGC CTCCATGAAGATAAACTCTGGGCCCGCCCACCGGCAGGACCTGTCGACCTGAGGTGACCCTGGGC T C RAVER1,AC011511.4 Ensembl:ENSG00000161847,Ensembl:ENSG00000267303 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10316344..10316417 26863196 MeRIP-seq:(Medium) rs969404676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512059,Human_RBP_ID_5190458,Human_RBP_ID_13357610,Human_RBP_ID_17272025,Human_RBP_ID_17386657,Human_RBP_ID_17914158,Human_RBP_ID_27266771 Human_miRNA_ID_272415,Human_miRNA_ID_272416,Human_miRNA_ID_1093897,Human_miRNA_ID_1093898 81609 RMVar_ID_81609 Human_SNP_ID_658164338 m1A Human chr19 - 10320784 10320784 10320784 CGCCCAGCTGAGGGCCCCCCAACTAACCCCCCAGCCCCTGGAGGTGGCAGCAGCAGCAGCAAAGC CGCCCAGCTGAGGGCCCCCCAACTAACCCCCCCGCCCCTGGAGGTGGCAGCAGCAGCAGCAAAGC T G RAVER1 Ensembl:ENSG00000161847 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10320735..10320846 26863196 MeRIP-seq:(Medium) rs1284880295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910552 Human_miRNA_ID_1358086,Human_miRNA_ID_2017113,Human_miRNA_ID_2686095 RMVar_hsa_circ_38589,RMVar_hsa_circ_51169,RMVar_hsa_circ_86550,RMVar_hsa_circ_4985,RMVar_hsa_circ_192342 81610 RMVar_ID_81610 Human_SNP_ID_658168154 m1A Human chr19 - 10333486 10333486 10333486 GGTTTCCCAAGATGGCGGCGGACGTGTCCGTTACTCACCGGCCCCCGCTGAGCCCTAAGTCTGGG GGTTTCCCAAGATGGCGGCGGACGTGTCCGTTTCTCACCGGCCCCCGCTGAGCCCTAAGTCTGGG T A RAVER1 Ensembl:ENSG00000161847 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10333239..10333525 26863196 MeRIP-seq:(Medium) rs375403160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55490,Human_RBP_ID_512101,Human_RBP_ID_4558053,Human_RBP_ID_8839745,Human_RBP_ID_9293364,Human_RBP_ID_22069689,Human_RBP_ID_22448367 81611 RMVar_ID_81611 Human_SNP_ID_658168406 m1A Human chr19 + 10334023 10334023 10334023 GTACGATAGTCACCACGCCCAGGGTCAGTAACACCGCCACGAAGACGGGGACAAAGTGGGAGCTC GTACGATAGTCACCACGCCCAGGGTCAGTAACCCCGCCACGAAGACGGGGACAAAGTGGGAGCTC A C AC114271.1 Ensembl:ENSG00000274425 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10333975..10334676 32194978 MeRIP-seq:(Medium) rs747026668 Functional Loss SNV dbSNP153 33..33 33 - - - 81612 RMVar_ID_81612 Human_SNP_ID_658174395 m1A Human chr19 + 10353963 10353963 10353963 TGGGGTTGAGAGTCTCTAATTGGCTAGGCCAGACTGGCCCCGCCCACAAGGCCACACCCACGCTC TGGGGTTGAGAGTCTCTAATTGGCTAGGCCAGGCTGGCCCCGCCCACAAGGCCACACCCACGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10353927..10354045 26863196 MeRIP-seq:(Medium) rs952288870 Functional Loss SNV dbSNP153 33..33 33 - - - 81613 RMVar_ID_81613 Human_SNP_ID_658176796 m1A Human chr19 + 10361842 10361842 10361842 ACCACTCGTAGCTCCTGCCCACGGTCCCTGCCAGGCACGAGGGGGTCCTCGTCATCCATCTTGCC ACCACTCGTAGCTCCTGCCCACGGTCCCTGCCTGGCACGAGGGGGTCCTCGTCATCCATCTTGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10361776..10361950 26863196 MeRIP-seq:(Medium) rs773984009 Functional Loss SNV dbSNP153 33..33 33 - - - 81614 RMVar_ID_81614 Human_SNP_ID_658177053 m1A Human chr19 + 10362428 10362428 10362428 CCCCGTCCTGCTGCTCAATGGGGAACTTTCGGAGCCGCAAGCTCTGCATGCCGTCTGGTGCCTGG CCCCGTCCTGCTGCTCAATGGGGAACTTTCGGGGCCGCAAGCTCTGCATGCCGTCTGGTGCCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10362377..10362465 26863196 MeRIP-seq:(Medium) rs1357623241 Functional Loss SNV dbSNP153 33..33 33 - - - 81615 RMVar_ID_81615 Human_SNP_ID_658177157 m1A Human chr19 - 10362643 10362643 10362643 CCCTGGACCACCTTCCAGGGAGCCATTTGTGCAGGCCAAGCTGCGGCCCGAGGACGGCCTGTACC CCCTGGACCACCTTCCAGGGAGCCATTTGTGCGGGCCAAGCTGCGGCCCGAGGACGGCCTGTACC T C TYK2 Ensembl:ENSG00000105397 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10361529..10362650 32194978 MeRIP-seq:(Medium) rs1255229652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769728,Human_RBP_ID_910571,Human_RBP_ID_3954425,Human_RBP_ID_5371279,Human_RBP_ID_5526817,Human_RBP_ID_23210850 Human_Splice_Rec_1954380,Human_Splice_Rec_1954381,Human_Splice_Rec_1954424,Human_Splice_Rec_1954425,Human_Splice_Rec_1954472,Human_Splice_Rec_1954473,Human_Splice_Rec_1954558,Human_Splice_Rec_1954559,Human_Splice_Rec_1954590 RMVar_hsa_circ_88271,RMVar_hsa_circ_27902,RMVar_hsa_circ_82488,RMVar_hsa_circ_192345,RMVar_hsa_circ_192348,RMVar_hsa_circ_79351,RMVar_hsa_circ_192347,RMVar_hsa_circ_113418,RMVar_hsa_circ_14473,RMVar_hsa_circ_336536,RMVar_hsa_circ_192349 81616 RMVar_ID_81616 Human_SNP_ID_658178013 m1A Human chr19 + 10365604 10365604 10365604 GTCACCAGCACCTCGTGGGTTGGGGGCCCAGCAGCAGACTCAGGGCCAGGGTCTGTAGGGGCCAC GTCACCAGCACCTCGTGGGTTGGGGGCCCAGCGGCAGACTCAGGGCCAGGGTCTGTAGGGGCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10365555..10365663 26863196 MeRIP-seq:(Medium) rs750764159 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_386 81617 RMVar_ID_81617 Human_SNP_ID_658182645 m1A Human chr19 + 10379783 10379783 10379783 TTCCGCATATTACACATTCAGCACAGACCCTGATTCAGGCACACACAAAAAGAACAAATATGACC TTCCGCATATTACACATTCAGCACAGACCCTGCTTCAGGCACACACAAAAAGAACAAATATGACC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10379776..10379800 32194978 MeRIP-seq:(Medium) rs1192728497 Functional Loss SNV dbSNP153 33..33 33 - - - 81618 RMVar_ID_81618 Human_SNP_ID_658182814 m1A Human chr19 - 10380461 10380461 10380461 GCGCGGAAGGAGCGCGGCCGGAGGTCCTCAGGAAGAAGCCGCGGGGACTGGCTGCGCTTGACAGG GCGCGGAAGGAGCGCGGCCGGAGGTCCTCAGGCAGAAGCCGCGGGGACTGGCTGCGCTTGACAGG T G TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:10380344..10380541;chr19:10380348..10380566;chr19:10380333..10380560;chr19:10380376..10380529 26863196 MeRIP-seq:(Medium) rs1332884103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770834,Human_RBP_ID_4558059,Human_RBP_ID_18420849 Human_Splice_Rec_1954455,Human_Splice_Rec_1954541,Human_Splice_Rec_1954597,Human_Splice_Rec_1954605 RMVar_hsa_circ_88271,RMVar_hsa_circ_192345 81619 RMVar_ID_81619 Human_SNP_ID_658186055 m1A Human chr19 - 10391243 10391243 10391243 GCTGGTCTACCAGGTAGTTGGGGAGGGTCCCCAGCCAAGGGGCCGGCTCTCGTCACTGGGCTCTG GCTGGTCTACCAGGTAGTTGGGGAGGGTCCCCGGCCAAGGGGCCGGCTCTCGTCACTGGGCTCTG T C CDC37 Ensembl:ENSG00000105401 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10391195..10391628 26863196 MeRIP-seq:(Medium) rs1161948128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53280,Human_RBP_ID_512123,Human_RBP_ID_770835,Human_RBP_ID_915216,Human_RBP_ID_1879493,Human_RBP_ID_5526828,Human_RBP_ID_8476161,Human_RBP_ID_9084250,Human_RBP_ID_17655511,Human_RBP_ID_17914207,Human_RBP_ID_18191945,Human_RBP_ID_18721395,Human_RBP_ID_22228520,Human_RBP_ID_26463960 Human_miRNA_ID_1358088,Human_miRNA_ID_2218714,Human_miRNA_ID_2686097 RMVar_hsa_circ_81442,RMVar_hsa_circ_96206,RMVar_hsa_circ_119354,RMVar_hsa_circ_112192,RMVar_hsa_circ_84394,RMVar_hsa_circ_192353,RMVar_hsa_circ_192355,RMVar_hsa_circ_76997,RMVar_hsa_circ_192356,RMVar_hsa_circ_192354,RMVar_hsa_circ_192351,RMVar_hsa_circ_192352 81620 RMVar_ID_81620 Human_SNP_ID_658186066 m1A Human chr19 - 10391280 10391280 10391280 AAGGCCCGGGGGTCCGGGGAAGGGCAGAGGTCACCAGGCTGGTCTACCAGGTAGTTGGGGAGGGT AAGGCCCGGGGGTCCGGGGAAGGGCAGAGGTCCCCAGGCTGGTCTACCAGGTAGTTGGGGAGGGT T G CDC37 Ensembl:ENSG00000105401 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:10391176..10391725;chr19:10391176..10391682 32194978 MeRIP-seq:(Medium) rs3198111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53280,Human_RBP_ID_239725,Human_RBP_ID_512123,Human_RBP_ID_826261,Human_RBP_ID_915216,Human_RBP_ID_1012758,Human_RBP_ID_4560905,Human_RBP_ID_5526828,Human_RBP_ID_6717113,Human_RBP_ID_8255754,Human_RBP_ID_17656735,Human_RBP_ID_17914207,Human_RBP_ID_18191945,Human_RBP_ID_22966322,Human_RBP_ID_26471974 Human_miRNA_ID_468489,Human_miRNA_ID_606646,Human_miRNA_ID_2464370,Human_miRNA_ID_2561223 RMVar_hsa_circ_81442,RMVar_hsa_circ_96206,RMVar_hsa_circ_119354,RMVar_hsa_circ_112192,RMVar_hsa_circ_84394,RMVar_hsa_circ_192353,RMVar_hsa_circ_192355,RMVar_hsa_circ_76997,RMVar_hsa_circ_192356,RMVar_hsa_circ_192354,RMVar_hsa_circ_192351,RMVar_hsa_circ_192352 81621 RMVar_ID_81621 Human_SNP_ID_658186138 m1A Human chr19 + 10391502 10391502 10391502 CGGGCGAGATGGCATCTATCTGTTTTCTGAAAAGGGGCACATAGGGGCCTGGAAGCAGGTGGCGG CGGGCGAGATGGCATCTATCTGTTTTCTGAAAGGGGGCACATAGGGGCCTGGAAGCAGGTGGCGG A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10391451..10391550 26863196 MeRIP-seq:(Medium) rs781724129 Functional Loss SNV dbSNP153 33..33 33 - - - 81622 RMVar_ID_81622 Human_SNP_ID_658186149 m1A Human chr19 + 10391526 10391526 10391526 TTCTGAAAAGGGGCACATAGGGGCCTGGAAGCAGGTGGCGGTGGTAGCTGGGGCAGGTCACACAC TTCTGAAAAGGGGCACATAGGGGCCTGGAAGCGGGTGGCGGTGGTAGCTGGGGCAGGTCACACAC A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:10391476..10391550 26863196 MeRIP-seq:(Medium) rs1159022882 Functional Loss SNV dbSNP153 33..33 33 - - - 81623 RMVar_ID_81623 Human_SNP_ID_658186631 m1A Human chr19 + 10393170 10393170 10393170 TCGAAGCACTTCTGGAGTTCCTGGGGGTACAGAGGGGCTGGGGTCAGGGGCTGGGTCCCTGTGGC TCGAAGCACTTCTGGAGTTCCTGGGGGTACAGTGGGGCTGGGGTCAGGGGCTGGGTCCCTGTGGC A T lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10393158..10393253 26863410 MeRIP-seq:(Medium) rs1490651402 Functional Loss SNV dbSNP153 33..33 33 - - - 81624 RMVar_ID_81624 Human_SNP_ID_658186722 m1A Human chr19 - 10393350 10393350 10393350 TGTGCGGGGCCGTGCCAAGCTGCGCATCGAGAAGGCCATGAAGGAGTACGAGGAGGAGGAGCGCA TGTGCGGGGCCGTGCCAAGCTGCGCATCGAGAGGGCCATGAAGGAGTACGAGGAGGAGGAGCGCA T C CDC37 Ensembl:ENSG00000105401 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10393299..10393481 26863196 MeRIP-seq:(Medium) rs1008098745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53285,Human_RBP_ID_4498396,Human_RBP_ID_8839075,Human_RBP_ID_9294191,Human_RBP_ID_23780879,Human_RBP_ID_26334829 Human_Splice_Rec_1954622,Human_Splice_Rec_1954623,Human_Splice_Rec_1954634,Human_Splice_Rec_1954635,Human_Splice_Rec_1954642,Human_Splice_Rec_1954643,Human_Splice_Rec_1954647,Human_Splice_Rec_1954649,Human_Splice_Rec_1954658,Human_Splice_Rec_1954659,Human_Splice_Rec_1954672,Human_Splice_Rec_1954678,Human_Splice_Rec_1954684 RMVar_hsa_circ_119354,RMVar_hsa_circ_112192,RMVar_hsa_circ_84394,RMVar_hsa_circ_192353,RMVar_hsa_circ_192355,RMVar_hsa_circ_76997,RMVar_hsa_circ_192356,RMVar_hsa_circ_192354,RMVar_hsa_circ_118024,RMVar_hsa_circ_192357 81625 RMVar_ID_81625 Human_SNP_ID_658187382 m1A Human chr19 - 10395492 10395489 10395492 CCGAGAAGACGGAGGAGGACTCAGAGGAGGTGAGGGAGCAGAAACACAAGACCTTCGTGGAAAAA CCGAGAAGACGGAGGAGGACTCAGAGGAGGTG___GAGCAGAAACACAAGACCTTCGTGGAAAAA CCCT C CDC37 Ensembl:ENSG00000105401 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10395226..10395612 26863196 MeRIP-seq:(Medium) rs759704031 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_239731,Human_RBP_ID_770844,Human_RBP_ID_4498412,Human_RBP_ID_9380417,Human_RBP_ID_17655512,Human_RBP_ID_26334832,Human_RBP_ID_27815091 Human_Splice_Rec_1954616,Human_Splice_Rec_1954617,Human_Splice_Rec_1954630,Human_Splice_Rec_1954654,Human_Splice_Rec_1954667,Human_Splice_Rec_1954673,Human_Splice_Rec_1954690 Human_miRNA_ID_208454,Human_miRNA_ID_1423522,Human_miRNA_ID_2017116 RMVar_hsa_circ_119354,RMVar_hsa_circ_84394,RMVar_hsa_circ_192355,RMVar_hsa_circ_192356,RMVar_hsa_circ_126183,RMVar_hsa_circ_192360 81626 RMVar_ID_81626 Human_SNP_ID_658187652 m1A Human chr19 - 10395980 10395978 10395981 GGAGCAGAAGCTGGAGGAGATGCGCAAGAAGGAGAAGAGCATGCCCTGGAACGTGGACACGCTCA GGAGCAGAAGCTGGAGGAGATGCGCAAGAAG___AAGAGCATGCCCTGGAACGTGGACACGCTCA TCTC T CDC37 Ensembl:ENSG00000105401 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10395924..10396225 26863196 MeRIP-seq:(Medium) rs756600464 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_239732,Human_RBP_ID_512148,Human_RBP_ID_826266,Human_RBP_ID_910579,Human_RBP_ID_5585228,Human_RBP_ID_8839076,Human_RBP_ID_9380419,Human_RBP_ID_18470493,Human_RBP_ID_22977640,Human_RBP_ID_26335611,Human_RBP_ID_27815093 Human_Splice_Rec_1954615,Human_Splice_Rec_1954629,Human_Splice_Rec_1954653,Human_Splice_Rec_1954665,Human_Splice_Rec_1954679,Human_Splice_Rec_1954689 RMVar_hsa_circ_119354,RMVar_hsa_circ_84394,RMVar_hsa_circ_192355,RMVar_hsa_circ_192356,RMVar_hsa_circ_126183,RMVar_hsa_circ_192360 81627 RMVar_ID_81627 Human_SNP_ID_658187659 m1A Human chr19 + 10396001 10396001 10396001 GCATGCTCTTCTCCTTCTTGCGCATCTCCTCCAGCTTCTGCTCCCAGCTCCGCTCCTCCTTGCGC GCATGCTCTTCTCCTTCTTGCGCATCTCCTCCCGCTTCTGCTCCCAGCTCCGCTCCTCCTTGCGC A C lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10395951..10396269 26863196 MeRIP-seq:(Medium) rs766695587 Functional Loss SNV dbSNP153 33..33 33 - - - 81628 RMVar_ID_81628 Human_SNP_ID_658189546 m1A Human chr19 - 10403454 10403454 10403454 AGGCAAGATGGTGGACTACAGCGTGTGGGACCACATTGAGGTGTCTGATGATGAAGACGAGACGC AGGCAAGATGGTGGACTACAGCGTGTGGGACCGCATTGAGGTGTCTGATGATGAAGACGAGACGC T C CDC37 Ensembl:ENSG00000105401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10403313..10403550 26863196 MeRIP-seq:(Medium) rs527724634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53293,Human_RBP_ID_512155,Human_RBP_ID_1012771,Human_RBP_ID_1553603,Human_RBP_ID_1879501,Human_RBP_ID_3562309,Human_RBP_ID_4558061,Human_RBP_ID_8476183,Human_RBP_ID_8829206,Human_RBP_ID_17914218,Human_RBP_ID_18721414 Human_Splice_Rec_1954613,Human_Splice_Rec_1954627,Human_Splice_Rec_1954651,Human_Splice_Rec_1954663,Human_Splice_Rec_1954685 RMVar_hsa_circ_84394,RMVar_hsa_circ_192356 81629 RMVar_ID_81629 Human_SNP_ID_658189556 m1A Human chr19 - 10403487 10403487 10403487 CCGCCACCCGAGCCGGAGCGGGCTGGGCCGCCAAGGCAAGATGGTGGACTACAGCGTGTGGGACC CCGCCACCCGAGCCGGAGCGGGCTGGGCCGCCGAGGCAAGATGGTGGACTACAGCGTGTGGGACC T C CDC37,MIR1181 Ensembl:ENSG00000105401,Ensembl:ENSG00000284268 Protein coding,miRNA 5'UTR,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10403401..10403575 26863410 MeRIP-seq:(Medium) rs775786517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553604,Human_RBP_ID_4558062,Human_RBP_ID_8840505,Human_RBP_ID_9381954,Human_RBP_ID_9428504,Human_RBP_ID_17670343,Human_RBP_ID_22371224,Human_RBP_ID_24545740,Human_RBP_ID_24559938 Human_miRNA_ID_2218716,Human_miRNA_ID_3130488 RMVar_hsa_circ_84394,RMVar_hsa_circ_192356 81630 RMVar_ID_81630 Human_SNP_ID_658189557 m1A Human chr19 - 10403487 10403487 10403487 CCGCCACCCGAGCCGGAGCGGGCTGGGCCGCCAAGGCAAGATGGTGGACTACAGCGTGTGGGACC CCGCCACCCGAGCCGGAGCGGGCTGGGCCGCCCAGGCAAGATGGTGGACTACAGCGTGTGGGACC T G CDC37,MIR1181 Ensembl:ENSG00000105401,Ensembl:ENSG00000284268 Protein coding,miRNA 5'UTR,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10403401..10403575 26863410 MeRIP-seq:(Medium) rs775786517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553604,Human_RBP_ID_4558062,Human_RBP_ID_8840505,Human_RBP_ID_9381954,Human_RBP_ID_9428504,Human_RBP_ID_17670343,Human_RBP_ID_22371224,Human_RBP_ID_24545740,Human_RBP_ID_24559938 Human_miRNA_ID_2218716,Human_miRNA_ID_3130488 RMVar_hsa_circ_84394,RMVar_hsa_circ_192356 81631 RMVar_ID_81631 Human_SNP_ID_658197002 m1A Human chr19 - 10430973 10430961 10430974 CTGGCGAAGAAGACGGGCGAGGAGGGCGGCGAACGCGGGCGGCGGGGCGCGCGCGGGGCCAGGGG CTGGCGAAGAAGACGGGCGAGGAGGGCGGCG_____________GGGCGCGCGCGGGGCCAGGGG CCGCCGCCCGCGTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10430835..10431034 26863196 MeRIP-seq:(Medium) rs769713868 Functional Loss DEL dbSNP153 32..44 33 - - - 81632 RMVar_ID_81632 Human_SNP_ID_658199274 m1A Human chr19 - 10439534 10439534 10439534 TGCTCCGATTCCTCCCCACTCACAAACAATCCATTCCTACCTGCTGTTGAGAGAACCACTGTAAC TGCTCCGATTCCTCCCCACTCACAAACAATCCGTTCCTACCTGCTGTTGAGAGAACCACTGTAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10439531..10439609 26863196 MeRIP-seq:(Medium) rs573616423 Functional Loss SNV dbSNP153 33..33 33 - - - 81633 RMVar_ID_81633 Human_SNP_ID_658216663 m1A Human chr19 + 10500059 10500059 10500059 GCTGCATGGGGTTCCAGAAGATAAGCAACACCACCACCTCTGGCACTCAGGGACCTGGAGGGGAG GCTGCATGGGGTTCCAGAAGATAAGCAACACCGCCACCTCTGGCACTCAGGGACCTGGAGGGGAG A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10499959..10500100 26863410 MeRIP-seq:(Medium) rs966252738 Functional Loss SNV dbSNP153 33..33 33 - - - 81634 RMVar_ID_81634 Human_SNP_ID_658217521 m1A Human chr19 - 10503320 10503320 10503320 TCGGGCGTCCCGAGGCCGCTCCCCAACCGACAACCAAGACCCCGCAGGCCACGCAGCCCTGGAGC TCGGGCGTCCCGAGGCCGCTCCCCAACCGACAGCCAAGACCCCGCAGGCCACGCAGCCCTGGAGC T C KEAP1 Ensembl:ENSG00000079999 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10503225..10503342 26863196 MeRIP-seq:(Medium) rs1448384472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1954869,Human_Splice_Rec_1954899 81635 RMVar_ID_81635 Human_SNP_ID_658229432 m1A Human chr19 - 10543989 10543989 10543989 GCAGCCGGTTCACGGGGCCCGGGGAAGGCGCTACTCGGCCCCCGTCCCCAGGGTACCGGGCCAGG GCAGCCGGTTCACGGGGCCCGGGGAAGGCGCTGCTCGGCCCCCGTCCCCAGGGTACCGGGCCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10543942..10544074 26863196 MeRIP-seq:(Medium) rs1461836835 Functional Loss SNV dbSNP153 33..33 33 - - - 81636 RMVar_ID_81636 Human_SNP_ID_658229742 m1A Human chr19 + 10544849 10544849 10544849 GATCTCCAGCATCCACCTCTGTGGCCGCCGCTACCGTTTCGAGGGCGAGGGTGAGCTGGTGGTTG GATCTCCAGCATCCACCTCTGTGGCCGCCGCTGCCGTTTCGAGGGCGAGGGTGAGCTGGTGGTTG A G ATG4D Ensembl:ENSG00000130734 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10544241..10544872 32194978 MeRIP-seq:(Medium) rs748069415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954429 Human_Splice_Rec_1954921,Human_Splice_Rec_1954938,Human_Splice_Rec_1954939,Human_Splice_Rec_1954957,Human_Splice_Rec_1954964,Human_Splice_Rec_1954965,Human_Splice_Rec_1954980,Human_Splice_Rec_1954981,Human_Splice_Rec_1954988,Human_Splice_Rec_1954989,Human_Splice_Rec_1955004,Human_Splice_Rec_1955008,Human_Splice_Rec_1955009 81637 RMVar_ID_81637 Human_SNP_ID_658232353 m1A Human chr19 - 10553128 10553128 10553128 ACCATCATCACTGCCAGAGCTCAAGATCCCACACCCGACATGACATAAATAAAAAAATAAATAGT ACCATCATCACTGCCAGAGCTCAAGATCCCACCCCCGACATGACATAAATAAAAAAATAAATAGT T G KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10553077..10553376 32194978 MeRIP-seq:(Medium) rs1219829332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1879510,Human_RBP_ID_2555466,Human_RBP_ID_3562322,Human_RBP_ID_8476223,Human_RBP_ID_13358374,Human_RBP_ID_27462786 81638 RMVar_ID_81638 Human_SNP_ID_658232648 m1A Human chr19 - 10553965 10553965 10553965 TGGGCCGGCAGCGGAGGAAACAACAGGGGCCCAAGAACAGCTCCTGAGCACCAGGGAGCAGGCAG TGGGCCGGCAGCGGAGGAAACAACAGGGGCCCCAGAACAGCTCCTGAGCACCAGGGAGCAGGCAG T G KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10553920..10555321 32194978 MeRIP-seq:(Medium) rs151313345 Functional Loss SNV dbSNP153 33..33 33 - - - 81639 RMVar_ID_81639 Human_SNP_ID_658233955 m1A Human chr19 - 10557897 10557897 10557897 GGGCTGGTGGGATCTGACCTGTGCGTCCTGGCAGATGGACGCCGACTACGACCCCAGCCAGCCGA GGGCTGGTGGGATCTGACCTGTGCGTCCTGGCGGATGGACGCCGACTACGACCCCAGCCAGCCGA T C KRI1 Ensembl:ENSG00000129347 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10557770..10558095 32194978 MeRIP-seq:(Medium) rs764035524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369955,Human_RBP_ID_23130608 RMVar_hsa_circ_28142,RMVar_hsa_circ_52276 81640 RMVar_ID_81640 Human_SNP_ID_658234038 m1A Human chr19 - 10558060 10558060 10558060 TGGCCCCACCTGTCTGTTCTCCCTGCATCCAGACGACTGGAACTGGGACACGTGGGACGGGCCTG TGGCCCCACCTGTCTGTTCTCCCTGCATCCAGTCGACTGGAACTGGGACACGTGGGACGGGCCTG T A KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10557976..10559700 26863196 MeRIP-seq:(Medium) rs1345639048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55265,Human_RBP_ID_8829225,Human_RBP_ID_23257718 Human_Splice_Rec_1955066,Human_Splice_Rec_1955067,Human_Splice_Rec_1955100,Human_Splice_Rec_1955101,Human_Splice_Rec_1955136,Human_Splice_Rec_1955137,Human_Splice_Rec_1955152,Human_Splice_Rec_1955153,Human_Splice_Rec_1955190,Human_Splice_Rec_1955191,Human_Splice_Rec_1955222,Human_Splice_Rec_1955223,Human_Splice_Rec_1955234,Human_Splice_Rec_1955235,Human_Splice_Rec_1955241,Human_Splice_Rec_1955262,Human_Splice_Rec_1955263 RMVar_hsa_circ_28142,RMVar_hsa_circ_52276,RMVar_hsa_circ_192379,RMVar_hsa_circ_95382 81641 RMVar_ID_81641 Human_SNP_ID_658234115 m1A Human chr19 - 10558238 10558238 10558238 GCTCTGGTAACCGCCAGCCCTGACCCTGCAGAAGTGCTTTGGGGACGAGTACTACGGGGCCGTGG GCTCTGGTAACCGCCAGCCCTGACCCTGCAGAGGTGCTTTGGGGACGAGTACTACGGGGCCGTGG T C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10558194..10559611 32194978 MeRIP-seq:(Medium) rs529360366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2555473 Human_Splice_Rec_1955064,Human_Splice_Rec_1955065,Human_Splice_Rec_1955098,Human_Splice_Rec_1955099,Human_Splice_Rec_1955134,Human_Splice_Rec_1955135,Human_Splice_Rec_1955150,Human_Splice_Rec_1955151,Human_Splice_Rec_1955188,Human_Splice_Rec_1955189,Human_Splice_Rec_1955220,Human_Splice_Rec_1955221,Human_Splice_Rec_1955260,Human_Splice_Rec_1955261 RMVar_hsa_circ_28142,RMVar_hsa_circ_52276 81642 RMVar_ID_81642 Human_SNP_ID_658234507 m1A Human chr19 - 10559411 10559408 10559411 AGTAACAGGCAACGAGATGCTGGGCCTCGAGGAGGGGGACCTTGAAGACGACTTCGACCCTGCCC AGTAACAGGCAACGAGATGCTGGGCCTCGAGG___GGGACCTTGAAGACGACTTCGACCCTGCCC CCCT C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10559299..10559450 26863196 MeRIP-seq:(Medium) rs746936591 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_6717225,Human_RBP_ID_9380428,Human_RBP_ID_24545422,Human_RBP_ID_26337374,Human_RBP_ID_26769794,Human_RBP_ID_27816050 Human_Splice_Rec_1955063,Human_Splice_Rec_1955097,Human_Splice_Rec_1955133,Human_Splice_Rec_1955149,Human_Splice_Rec_1955187,Human_Splice_Rec_1955219,Human_Splice_Rec_1955233,Human_Splice_Rec_1955259 RMVar_hsa_circ_52276,RMVar_hsa_circ_56596,RMVar_hsa_circ_346936 81643 RMVar_ID_81643 Human_SNP_ID_658234508 m1A Human chr19 - 10559411 10559409 10559411 AGTAACAGGCAACGAGATGCTGGGCCTCGAGGAGGGGGACCTTGAAGACGACTTCGACCCTGCCC AGTAACAGGCAACGAGATGCTGGGCCTCGAGG__GGGGACCTTGAAGACGACTTCGACCCTGCCC CCT C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10559299..10559450 26863196 MeRIP-seq:(Medium) rs1337706680 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6717225,Human_RBP_ID_9380428,Human_RBP_ID_24545422,Human_RBP_ID_26337374,Human_RBP_ID_26769794,Human_RBP_ID_27816050 Human_Splice_Rec_1955063,Human_Splice_Rec_1955097,Human_Splice_Rec_1955133,Human_Splice_Rec_1955149,Human_Splice_Rec_1955187,Human_Splice_Rec_1955219,Human_Splice_Rec_1955233,Human_Splice_Rec_1955259 RMVar_hsa_circ_52276,RMVar_hsa_circ_56596,RMVar_hsa_circ_346936 81644 RMVar_ID_81644 Human_SNP_ID_658235205 m1A Human chr19 - 10561218 10561218 10561218 GGAGGACAGTGAGGACGAGGACGGCGCTGGGGAGGGCGGCTCCAGTTTGCTGCAGAAACGTGCCA GGAGGACAGTGAGGACGAGGACGGCGCTGGGGCGGGCGGCTCCAGTTTGCTGCAGAAACGTGCCA T G KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:10561071..10561339 26863196 MeRIP-seq:(Medium) rs11545166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55274,Human_RBP_ID_241533,Human_RBP_ID_773831,Human_RBP_ID_5585245,Human_RBP_ID_6717227,Human_RBP_ID_26335629,Human_RBP_ID_26769983,Human_RBP_ID_27815105 Human_Splice_Rec_1955052,Human_Splice_Rec_1955053,Human_Splice_Rec_1955086,Human_Splice_Rec_1955087,Human_Splice_Rec_1955122,Human_Splice_Rec_1955123,Human_Splice_Rec_1955176,Human_Splice_Rec_1955177,Human_Splice_Rec_1955208,Human_Splice_Rec_1955209,Human_Splice_Rec_1955276,Human_Splice_Rec_1955277,Human_Splice_Rec_1955290,Human_Splice_Rec_1955291,Human_Splice_Rec_1955302,Human_Splice_Rec_1955303,Human_Splice_Rec_1955316,Human_Splice_Rec_1955317,Human_Splice_Rec_1955330 RMVar_hsa_circ_52276,RMVar_hsa_circ_56596 81645 RMVar_ID_81645 Human_SNP_ID_658235316 m1A Human chr19 + 10561627 10561627 10561627 TGAACCCGTGCCTATCCAACCCCCGAGCCTCAACTTTCCTCCATTGGGCCATTCCCGCCCACCCA TGAACCCGTGCCTATCCAACCCCCGAGCCTCACCTTTCCTCCATTGGGCCATTCCCGCCCACCCA A C lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10561625..10561850 26863196 MeRIP-seq:(Medium) rs1484416896 Functional Loss SNV dbSNP153 33..33 33 - - - 81646 RMVar_ID_81646 Human_SNP_ID_658235722 m1A Human chr19 + 10562774 10562774 10562774 AGATAACCTTCCTCTCGTAGTCCTTCAGGTACATGGGCCGCACTTTCTTCTGCTTCTCCAAGGCT AGATAACCTTCCTCTCGTAGTCCTTCAGGTACGTGGGCCGCACTTTCTTCTGCTTCTCCAAGGCT A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10562695..10562825 26863196 MeRIP-seq:(Medium) rs575503661 Functional Loss SNV dbSNP153 33..33 33 - - - 81647 RMVar_ID_81647 Human_SNP_ID_658236513 m1A Human chr19 - 10565428 10565428 10565428 CCCCCCCTTTCCTCTTTCATCCTCAAGAGTCTAGCCATTTTTTAGTGTACTCCTTGCGCCACGTG CCCCCCCTTTCCTCTTTCATCCTCAAGAGTCTGGCCATTTTTTAGTGTACTCCTTGCGCCACGTG T C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10565381..10565509 26863196 MeRIP-seq:(Medium) rs1219203486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131031,Human_RBP_ID_17082302 81648 RMVar_ID_81648 Human_SNP_ID_658236813 m1A Human chr19 - 10565963 10565956 10565963 CGGAACCGCGCGGGTCGTCGCAGCTGCGGGTGAACGCGGCGTTTGCCGCGCGGTACAACCGCTAC CGGAACCGCGCGGGTCGTCGCAGCTGCGGGTG_______CGTTTGCCGCGCGGTACAACCGCTAC GCCGCGTT G KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10565765..10566000 26863196 MeRIP-seq:(Medium) rs1380190597 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_4558068,Human_RBP_ID_5261195,Human_RBP_ID_22977645,Human_RBP_ID_27816057 Human_Splice_Rec_1955043,Human_Splice_Rec_1955075,Human_Splice_Rec_1955111,Human_Splice_Rec_1955165,Human_Splice_Rec_1955245,Human_Splice_Rec_1955267,Human_Splice_Rec_1955283,Human_Splice_Rec_1955295,Human_Splice_Rec_1955307,Human_Splice_Rec_1955319 81649 RMVar_ID_81649 Human_SNP_ID_658236813 m1A Human chr19 - 10565962 10565956 10565963 GGAACCGCGCGGGTCGTCGCAGCTGCGGGTGAACGCGGCGTTTGCCGCGCGGTACAACCGCTACC GGAACCGCGCGGGTCGTCGCAGCTGCGGGTG_______CGTTTGCCGCGCGGTACAACCGCTACC GCCGCGTT G KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10565701..10565989;chr19:10565588..10566025;chr19:10565726..10566025 26863196 MeRIP-seq:(Medium) rs1380190597 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_4558068,Human_RBP_ID_5261195,Human_RBP_ID_22977645,Human_RBP_ID_27816057 Human_Splice_Rec_1955043,Human_Splice_Rec_1955075,Human_Splice_Rec_1955111,Human_Splice_Rec_1955165,Human_Splice_Rec_1955245,Human_Splice_Rec_1955267,Human_Splice_Rec_1955283,Human_Splice_Rec_1955295,Human_Splice_Rec_1955307,Human_Splice_Rec_1955319 81650 RMVar_ID_81650 Human_SNP_ID_658236816 m1A Human chr19 - 10565962 10565962 10565962 GGAACCGCGCGGGTCGTCGCAGCTGCGGGTGAACGCGGCGTTTGCCGCGCGGTACAACCGCTACC GGAACCGCGCGGGTCGTCGCAGCTGCGGGTGAGCGCGGCGTTTGCCGCGCGGTACAACCGCTACC T C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10565701..10565989;chr19:10565588..10566025;chr19:10565726..10566025 26863196 MeRIP-seq:(Medium) rs1184094113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558068,Human_RBP_ID_5261195,Human_RBP_ID_22977645,Human_RBP_ID_27816057 Human_Splice_Rec_1955043,Human_Splice_Rec_1955075,Human_Splice_Rec_1955111,Human_Splice_Rec_1955165,Human_Splice_Rec_1955245,Human_Splice_Rec_1955267,Human_Splice_Rec_1955283,Human_Splice_Rec_1955295,Human_Splice_Rec_1955307,Human_Splice_Rec_1955319 81651 RMVar_ID_81651 Human_SNP_ID_658236817 m1A Human chr19 + 10565965 10565965 10565965 AGCGGTTGTACCGCGCGGCAAACGCCGCGTTCACCCGCAGCTGCGACGACCCGCGCGGTTCCGGC AGCGGTTGTACCGCGCGGCAAACGCCGCGTTCCCCCGCAGCTGCGACGACCCGCGCGGTTCCGGC A C lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr19:10565673..10566025;chr19:10565751..10566000 26863196,26863410 MeRIP-seq:(Medium) rs761352738 Functional Loss SNV dbSNP153 33..33 33 - - - 81652 RMVar_ID_81652 Human_SNP_ID_658239764 m1A Human chr19 - 10575031 10575029 10575031 CCCTCGTGTACCTGATGCCCCCATGTTCCCTCAGGGGGGCAAGGAGTACTTGATGCGAGCCCACT CCCTCGTGTACCTGATGCCCCCATGTTCCCTC__GGGGGCAAGGAGTACTTGATGCGAGCCCACT CCT C AP1M2 Ensembl:ENSG00000129354 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10575001..10575050 26863196 MeRIP-seq:(Medium) rs1296181187 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_23568,RMVar_hsa_circ_127146,RMVar_hsa_circ_192380 81653 RMVar_ID_81653 Human_SNP_ID_658240466 m1A Human chr19 - 10577283 10577283 10577283 GGAGATATCTGTGCCTGTACCCAGCGATGCCGACTCCCCCAGATTCAAGACCAGTGTGGGCAGCG GGAGATATCTGTGCCTGTACCCAGCGATGCCGGCTCCCCCAGATTCAAGACCAGTGTGGGCAGCG T C AP1M2 Ensembl:ENSG00000129354 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10577201..10577375 26863196 MeRIP-seq:(Medium) rs979201258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380431 Human_Splice_Rec_1955337,Human_Splice_Rec_1955358,Human_Splice_Rec_1955359,Human_Splice_Rec_1955380,Human_Splice_Rec_1955381,Human_Splice_Rec_1955387,Human_Splice_Rec_1955391,Human_Splice_Rec_1955406 RMVar_hsa_circ_23568,RMVar_hsa_circ_127146,RMVar_hsa_circ_192380,RMVar_hsa_circ_192383,RMVar_hsa_circ_48623,RMVar_hsa_circ_374203,RMVar_hsa_circ_342252,RMVar_hsa_circ_192384 81654 RMVar_ID_81654 Human_SNP_ID_658240475 m1A Human chr19 - 10577297 10577297 10577297 GTGGCCAACGGTGTGGAGATATCTGTGCCTGTACCCAGCGATGCCGACTCCCCCAGATTCAAGAC GTGGCCAACGGTGTGGAGATATCTGTGCCTGTTCCCAGCGATGCCGACTCCCCCAGATTCAAGAC T A AP1M2 Ensembl:ENSG00000129354 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:10577077..10577375;chr19:10577122..10577400 26863196 MeRIP-seq:(Medium) rs777088150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9380431 Human_Splice_Rec_1955337,Human_Splice_Rec_1955358,Human_Splice_Rec_1955359,Human_Splice_Rec_1955380,Human_Splice_Rec_1955381,Human_Splice_Rec_1955387,Human_Splice_Rec_1955391,Human_Splice_Rec_1955406 RMVar_hsa_circ_23568,RMVar_hsa_circ_127146,RMVar_hsa_circ_192380,RMVar_hsa_circ_192383,RMVar_hsa_circ_48623,RMVar_hsa_circ_374203,RMVar_hsa_circ_342252,RMVar_hsa_circ_192384 81655 RMVar_ID_81655 Human_SNP_ID_658250870 m1A Human chr19 - 10613681 10613680 10613681 ACTCTGCTACCACCCTCTTCCATTTTTCTTAAAGAGACGGGGTCTCACTATGTTGCCCAGGCTGG ACTCTGCTACCACCCTCTTCCATTTTTCTTAA_GAGACGGGGTCTCACTATGTTGCCCAGGCTGG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10613675..10613772 26863196 MeRIP-seq:(Medium) rs1568443428 Functional Loss DEL dbSNP153 33..33 33 - - - 81656 RMVar_ID_81656 Human_SNP_ID_658254109 m1A Human chr19 + 10625594 10625594 10625594 CTCCAGACTCGGGAGGGTCGAGGGGGCGCGGGAGAGAGCGCGGGCGGCCGCCGGGGCTGGTCGCC CTCCAGACTCGGGAGGGTCGAGGGGGCGCGGGGGAGAGCGCGGGCGGCCGCCGGGGCTGGTCGCC A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10625555..10625703 26863196 MeRIP-seq:(Medium) rs1017339284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4498746 Human_Splice_Rec_1955525,Human_Splice_Rec_1955535,Human_Splice_Rec_1955577,Human_Splice_Rec_1955619,Human_Splice_Rec_1955635 RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_192387 81657 RMVar_ID_81657 Human_SNP_ID_658259643 m1A Human chr19 - 10643351 10643351 10643351 AGGACTCCGCTGCCTTCTTGTTGGTCTTGTTCAAGAGTTTCTTGAGGGTGGAAGACATGAAGTAA AGGACTCCGCTGCCTTCTTGTTGGTCTTGTTCGAGAGTTTCTTGAGGGTGGAAGACATGAAGTAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10643301..10643400 32194978 MeRIP-seq:(Medium) rs748464396 Functional Loss SNV dbSNP153 33..33 33 - - - 81658 RMVar_ID_81658 Human_SNP_ID_658259913 m1A Human chr19 + 10644323 10644322 10644324 CACTTGATCCTTTTGCCAAACTTGTCAAACTCAGGGGAACTGGCTTCCCAGTTGCCCCTTTGCCA CACTTGATCCTTTTGCCAAACTTGTCAAACTC__GGGAACTGGCTTCCCAGTTGCCCCTTTGCCA CAG C SLC44A2 Ensembl:ENSG00000129353 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10644276..10644350 32194978 MeRIP-seq:(Medium) rs1485529509 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_279174,Human_RBP_ID_512272,Human_RBP_ID_17266529 Human_miRNA_ID_120447,Human_miRNA_ID_124264,Human_miRNA_ID_960250,Human_miRNA_ID_1973818,Human_miRNA_ID_1973819,Human_miRNA_ID_1975995,Human_miRNA_ID_1975996,Human_miRNA_ID_2613785,Human_miRNA_ID_2613786,Human_miRNA_ID_3004813,Human_miRNA_ID_3004814 RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_75772,RMVar_hsa_circ_192392,RMVar_hsa_circ_78359,RMVar_hsa_circ_192397,RMVar_hsa_circ_97561,RMVar_hsa_circ_79021,RMVar_hsa_circ_125737,RMVar_hsa_circ_192400,RMVar_hsa_circ_192401,RMVar_hsa_circ_192403,RMVar_hsa_circ_115978,RMVar_hsa_circ_117681,RMVar_hsa_circ_192407,RMVar_hsa_circ_111848,RMVar_hsa_circ_192409,RMVar_hsa_circ_192410 81659 RMVar_ID_81659 Human_SNP_ID_658259934 m1A Human chr19 - 10644427 10644427 10644427 GGAGACCCCCCCCTCTTTCCCCTGGGGCCAGGAGTTCTCCCTCTCCAGGATCCTGGGACAGTGCT GGAGACCCCCCCCTCTTTCCCCTGGGGCCAGGGGTTCTCCCTCTCCAGGATCCTGGGACAGTGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10644376..10644525 32194978 MeRIP-seq:(Medium) rs3859515 Functional Loss SNV dbSNP153 33..33 33 - - - 81660 RMVar_ID_81660 Human_SNP_ID_658263425 m1A Human chr19 - 10654744 10654744 10654744 GGCCGCGTGCGGGGGGGAGCGGCTGCGCGCGCACCGAGTCCTCGCCGCCGCCGCAGCCGCCATTT GGCCGCGTGCGGGGGGGAGCGGCTGCGCGCGCCCCGAGTCCTCGCCGCCGCCGCAGCCGCCATTT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10654732..10654951 26863196 MeRIP-seq:(Medium) rs1006026703 Functional Loss SNV dbSNP153 33..33 33 - - - 81661 RMVar_ID_81661 Human_SNP_ID_658268857 m1A Human chr19 - 10670574 10670574 10670574 TTTTTACTTCTTCTGTAGTGTCTGGAAATCAAACTTTTGCTTATCTTTTCAAATTGTGATAGAGT TTTTTACTTCTTCTGTAGTGTCTGGAAATCAAGCTTTTGCTTATCTTTTCAAATTGTGATAGAGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10670501..10670600 32194978 MeRIP-seq:(Medium) rs559438779 Functional Loss SNV dbSNP153 33..33 33 - - - 81662 RMVar_ID_81662 Human_SNP_ID_658268990 m1A Human chr19 + 10670953 10670953 10670953 TTGGGCTGCTTGCTCTCTTTACATCATTTTTAACTTAATTCTCACATCCCTAGCGTCCAATGCGA TTGGGCTGCTTGCTCTCTTTACATCATTTTTATCTTAATTCTCACATCCCTAGCGTCCAATGCGA A T ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10670951..10671025 32194978 MeRIP-seq:(Medium) rs752727711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18532246,Human_RBP_ID_25381559 RMVar_hsa_circ_4376,RMVar_hsa_circ_302792,RMVar_hsa_circ_362795,RMVar_hsa_circ_50296 81663 RMVar_ID_81663 Human_SNP_ID_658269034 m1A Human chr19 - 10671102 10671102 10671102 CCCTTTTCCTGCTCGTCTATCCAGTCGGACACAGCTTTGAGCGCCCGCTCCGTGTGGGACACCAT CCCTTTTCCTGCTCGTCTATCCAGTCGGACACCGCTTTGAGCGCCCGCTCCGTGTGGGACACCAT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10671051..10679950 32194978 MeRIP-seq:(Medium) rs754055267 Functional Loss SNV dbSNP153 33..33 33 - - - 81664 RMVar_ID_81664 Human_SNP_ID_658269063 m1A Human chr19 + 10671177 10671177 10671177 CAGGCAGAGTCCGATAACATGGATGTGCCCCCAGAGGACGACAGTAAAGAAGGGGCTGGGTAAGT CAGGCAGAGTCCGATAACATGGATGTGCCCCCGGAGGACGACAGTAAAGAAGGGGCTGGGTAAGT A G ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:10671019..10671245;chr19:10670951..10671227;chr19:10670951..10671232 26863196 MeRIP-seq:(Medium) rs759916313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512308,Human_RBP_ID_825395,Human_RBP_ID_913225,Human_RBP_ID_1553701,Human_RBP_ID_1879580,Human_RBP_ID_3954438,Human_RBP_ID_5585257,Human_RBP_ID_6717491,Human_RBP_ID_8839082,Human_RBP_ID_9084273,Human_RBP_ID_9380441,Human_RBP_ID_13359455,Human_RBP_ID_18165956,Human_RBP_ID_18440444,Human_RBP_ID_23781114,Human_RBP_ID_24545707,Human_RBP_ID_26334834 Human_Splice_Rec_1955715,Human_Splice_Rec_1955753,Human_Splice_Rec_1955791,Human_Splice_Rec_1955825,Human_Splice_Rec_1955861,Human_Splice_Rec_1955869,Human_Splice_Rec_1955875,Human_Splice_Rec_1955891,Human_Splice_Rec_1955903,Human_Splice_Rec_1955911,Human_Splice_Rec_1955943,Human_Splice_Rec_1955973,Human_Splice_Rec_1956009,Human_Splice_Rec_1956043,Human_Splice_Rec_1956057 Human_miRNA_ID_2425569,Human_miRNA_ID_2425570,Human_miRNA_ID_2435237,Human_miRNA_ID_2435238,Human_miRNA_ID_2571365,Human_miRNA_ID_2571366,Human_miRNA_ID_3045102,Human_miRNA_ID_3045103 RMVar_hsa_circ_4376,RMVar_hsa_circ_302792,RMVar_hsa_circ_362795,RMVar_hsa_circ_50296,RMVar_hsa_circ_14966,RMVar_hsa_circ_92401,RMVar_hsa_circ_108280,RMVar_hsa_circ_192411,RMVar_hsa_circ_192412 81665 RMVar_ID_81665 Human_SNP_ID_658272663 m1A Human chr19 + 10681306 10681304 10681307 GGAGGACGGGGAGGAGAAGTCGCCCAGCAAAAAGAAGAAGAAGATTCAGAAGAAAGGTACAGGCC GGAGGACGGGGAGGAGAAGTCGCCCAGCAAA___AAGAAGAAGATTCAGAAGAAAGGTACAGGCC AAAG A ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10681256..10681456 32194978 MeRIP-seq:(Medium) rs747091167 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_53775,Human_RBP_ID_240133,Human_RBP_ID_825405,Human_RBP_ID_913237,Human_RBP_ID_1067468,Human_RBP_ID_1879617,Human_RBP_ID_3956264,Human_RBP_ID_8255757,Human_RBP_ID_9380455,Human_RBP_ID_18532249,Human_RBP_ID_24545426,Human_RBP_ID_26334841,Human_RBP_ID_26981698,Human_RBP_ID_27815110 Human_Splice_Rec_1955730,Human_Splice_Rec_1955731,Human_Splice_Rec_1955768,Human_Splice_Rec_1955806,Human_Splice_Rec_1955807,Human_Splice_Rec_1955840,Human_Splice_Rec_1955841,Human_Splice_Rec_1955926,Human_Splice_Rec_1955927,Human_Splice_Rec_1955958,Human_Splice_Rec_1955959,Human_Splice_Rec_1955988,Human_Splice_Rec_1955989,Human_Splice_Rec_1956024,Human_Splice_Rec_1956025,Human_Splice_Rec_1956056,Human_Splice_Rec_1956068,Human_Splice_Rec_1956080,Human_Splice_Rec_1956081,Human_Splice_Rec_1956092,Human_Splice_Rec_1956098 Human_miRNA_ID_2005838,Human_miRNA_ID_2005839 RMVar_hsa_circ_362795,RMVar_hsa_circ_50296,RMVar_hsa_circ_23678,RMVar_hsa_circ_92401,RMVar_hsa_circ_192412,RMVar_hsa_circ_93559,RMVar_hsa_circ_192414,RMVar_hsa_circ_100977,RMVar_hsa_circ_192416,RMVar_hsa_circ_192415 81666 RMVar_ID_81666 Human_SNP_ID_658272886 m1A Human chr19 - 10681949 10681949 10681949 ATAGCAAGGTGGCTCTGGATCAGCACGATGGCAGGTCTCCACGAGAGCTCTGCCAATCCTAACCC ATAGCAAGGTGGCTCTGGATCAGCACGATGGCGGGTCTCCACGAGAGCTCTGCCAATCCTAACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10681948..10682131 26863196 MeRIP-seq:(Medium) rs1384543558 Functional Loss SNV dbSNP153 33..33 33 - - - 81667 RMVar_ID_81667 Human_SNP_ID_658273151 m1A Human chr19 + 10682595 10682595 10682595 GGGTGCTGAAGGCAGGGACTCGAGCAAGGGGGAGGACTCGGCTGAGGAGACCGAGGCGAAGCCAG GGGTGCTGAAGGCAGGGACTCGAGCAAGGGGGGGGACTCGGCTGAGGAGACCGAGGCGAAGCCAG A G ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10682524..10682742 26863196 MeRIP-seq:(Medium) rs1422037785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53783,Human_RBP_ID_240135,Human_RBP_ID_771435,Human_RBP_ID_825410,Human_RBP_ID_913243,Human_RBP_ID_1879633,Human_RBP_ID_3562400,Human_RBP_ID_3954450,Human_RBP_ID_4499016,Human_RBP_ID_5375661,Human_RBP_ID_6717628,Human_RBP_ID_9293377,Human_RBP_ID_9380465,Human_RBP_ID_13359958,Human_RBP_ID_17914320,Human_RBP_ID_18994317,Human_RBP_ID_22977648,Human_RBP_ID_26335652,Human_RBP_ID_27462837 Human_Splice_Rec_1955734,Human_Splice_Rec_1955770,Human_Splice_Rec_1955810,Human_Splice_Rec_1955844,Human_Splice_Rec_1955930,Human_Splice_Rec_1955962,Human_Splice_Rec_1955992,Human_Splice_Rec_1956028 RMVar_hsa_circ_50296,RMVar_hsa_circ_92401,RMVar_hsa_circ_192412,RMVar_hsa_circ_93559,RMVar_hsa_circ_100977,RMVar_hsa_circ_192416,RMVar_hsa_circ_192415,RMVar_hsa_circ_5258,RMVar_hsa_circ_14614,RMVar_hsa_circ_362879,RMVar_hsa_circ_192418,RMVar_hsa_circ_98084 81668 RMVar_ID_81668 Human_SNP_ID_658273771 m1A Human chr19 + 10683896 10683896 10683896 GGGTGGGCCGGAGACACTGCTGGACCCCGGTAACCCTGTCTTTCCCTTTCCAGGTGCTGGGTATG GGGTGGGCCGGAGACACTGCTGGACCCCGGTAGCCCTGTCTTTCCCTTTCCAGGTGCTGGGTATG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10683893..10683991 26863196 MeRIP-seq:(Medium) rs1023309195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369967,Human_RBP_ID_21977656,Human_RBP_ID_22666400,Human_RBP_ID_26784005 Human_Splice_Rec_1955743,Human_Splice_Rec_1955779,Human_Splice_Rec_1955819,Human_Splice_Rec_1955853,Human_Splice_Rec_1955939,Human_Splice_Rec_1956001,Human_Splice_Rec_1956037,Human_Splice_Rec_1956103,Human_Splice_Rec_1956107 RMVar_hsa_circ_50296,RMVar_hsa_circ_92401,RMVar_hsa_circ_192412,RMVar_hsa_circ_100977,RMVar_hsa_circ_192415,RMVar_hsa_circ_5258,RMVar_hsa_circ_192418,RMVar_hsa_circ_98084 81669 RMVar_ID_81669 Human_SNP_ID_658275496 m1A Human chr19 + 10688625 10688625 10688625 CTCAGGCGGGGCATCCTACAACCCAGGGTCACACGGGGGCTACGGCGGAGGTTCTGGGGGCGGCT CTCAGGCGGGGCATCCTACAACCCAGGGTCACGCGGGGGCTACGGCGGAGGTTCTGGGGGCGGCT A G ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10688575..10689275 32194978 MeRIP-seq:(Medium) rs1164685319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53806,Human_RBP_ID_240143,Human_RBP_ID_4561137,Human_RBP_ID_5526839,Human_RBP_ID_6717733,Human_RBP_ID_22741993,Human_RBP_ID_22966482,Human_RBP_ID_23781211 Human_Splice_Rec_1955746,Human_Splice_Rec_1955747,Human_Splice_Rec_1955784,Human_Splice_Rec_1955785,Human_Splice_Rec_1956004,Human_Splice_Rec_1956005,Human_Splice_Rec_1956040,Human_Splice_Rec_1956041,Human_Splice_Rec_1956108,Human_Splice_Rec_1956109,Human_Splice_Rec_1956112,Human_Splice_Rec_1956113,Human_Splice_Rec_1956116,Human_Splice_Rec_1956117 RMVar_hsa_circ_95061,RMVar_hsa_circ_192421,RMVar_hsa_circ_192420,RMVar_hsa_circ_377005 81670 RMVar_ID_81670 Human_SNP_ID_658275740 m1A Human chr19 + 10689260 10689260 10689260 CAGTGGCCCTCCCAGCTCCTACCAGTCCTCACAAGGCGGCTATGGCAGAAACGCAGACCACAGCA CAGTGGCCCTCCCAGCTCCTACCAGTCCTCACCAGGCGGCTATGGCAGAAACGCAGACCACAGCA A C ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10689153..10689501 26863196 MeRIP-seq:(Medium) rs867160929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53807,Human_RBP_ID_512389,Human_RBP_ID_5526840,Human_RBP_ID_13360167,Human_RBP_ID_17266556,Human_RBP_ID_18192865,Human_RBP_ID_22446423,Human_RBP_ID_22501539 Human_Splice_Rec_1955748,Human_Splice_Rec_1955786,Human_Splice_Rec_1956006,Human_Splice_Rec_1956042,Human_Splice_Rec_1956110,Human_Splice_Rec_1956114,Human_Splice_Rec_1956118 Human_miRNA_ID_3010977 RMVar_hsa_circ_95061,RMVar_hsa_circ_192420 81671 RMVar_ID_81671 Human_SNP_ID_658276037 m1A Human chr19 + 10689973 10689973 10689973 TCAGGATGGTCCCTGGTCCTTAGAGAGGGTCCAGTTCAGGCTTCTAGACATTTTACTCATGCTCA TCAGGATGGTCCCTGGTCCTTAGAGAGGGTCCGGTTCAGGCTTCTAGACATTTTACTCATGCTCA A G ILF3 Ensembl:ENSG00000129351 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10689923..10690323 32194978 MeRIP-seq:(Medium) rs923788091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512413,Human_RBP_ID_1553904,Human_RBP_ID_1879691,Human_RBP_ID_6717763,Human_RBP_ID_8476415,Human_RBP_ID_8829328,Human_RBP_ID_13360199,Human_RBP_ID_17914371 Human_miRNA_ID_1148308,Human_miRNA_ID_1228457,Human_miRNA_ID_1798348 RMVar_hsa_circ_95061,RMVar_hsa_circ_192420 81672 RMVar_ID_81672 Human_SNP_ID_658276329 m1A Human chr19 + 10690905 10690905 10690905 CTTTTGAGGAATTCTTATTTGTGTTAGAGCAGAGGAGGTCCCAGATACCAAGTGGCGCCTCCCAG CTTTTGAGGAATTCTTATTTGTGTTAGAGCAGCGGAGGTCCCAGATACCAAGTGGCGCCTCCCAG A C ILF3 Ensembl:ENSG00000129351 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10690855..10690994 26863196 MeRIP-seq:(Medium) rs1455446215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53810,Human_RBP_ID_5527222,Human_RBP_ID_6717786,Human_RBP_ID_13360243,Human_RBP_ID_18165651,Human_RBP_ID_26471992,Human_RBP_ID_26981839,Human_RBP_ID_27267077 Human_miRNA_ID_2479709 RMVar_hsa_circ_95061,RMVar_hsa_circ_192420 81673 RMVar_ID_81673 Human_SNP_ID_658276788 m1A Human chr19 + 10692315 10692315 10692315 TGCACTGCGCGGGCCTGAGACTGCTGGATACAATGTTGGGCAACAACTCAGCCAGCCTGATGGCA TGCACTGCGCGGGCCTGAGACTGCTGGATACAGTGTTGGGCAACAACTCAGCCAGCCTGATGGCA A G ILF3 Ensembl:ENSG00000129351 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10691967..10692317 32194978 MeRIP-seq:(Medium) rs1258174317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553932,Human_RBP_ID_1879720,Human_RBP_ID_3562451,Human_RBP_ID_8476438,Human_RBP_ID_13360289,Human_RBP_ID_17266576,Human_RBP_ID_17382033,Human_RBP_ID_17914401,Human_RBP_ID_18721709,Human_RBP_ID_22228815,Human_RBP_ID_27462923 Human_miRNA_ID_1715864 RMVar_hsa_circ_95061,RMVar_hsa_circ_192420 81674 RMVar_ID_81674 Human_SNP_ID_658279634 m1A Human chr19 + 10701502 10701502 10701502 GCAGCTACCCAGGCTTCCCTGGAGTCGGCCCCACGGATCATGCGGCTGGTGGCCGAATGCAGCCG GCAGCTACCCAGGCTTCCCTGGAGTCGGCCCCCCGGATCATGCGGCTGGTGGCCGAATGCAGCCG A C QTRT1 Ensembl:ENSG00000213339 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:10701451..10701650;chr19:10701451..10701675;chr19:10701451..10701700 26863196 MeRIP-seq:(Medium) rs1298145533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826862,Human_RBP_ID_4499287,Human_RBP_ID_5421125,Human_RBP_ID_5498860,Human_RBP_ID_13360368,Human_RBP_ID_18420851,Human_RBP_ID_23119168 RMVar_hsa_circ_192422,RMVar_hsa_circ_107548 81675 RMVar_ID_81675 Human_SNP_ID_658279673 m1A Human chr19 + 10701570 10701570 10701570 CAGGGCCCGGGCAGGCGAGCTGTGGCTGCCGCATGGGACAGTGGCCACTCCTGTGTTCATGCCAG CAGGGCCCGGGCAGGCGAGCTGTGGCTGCCGCGTGGGACAGTGGCCACTCCTGTGTTCATGCCAG A G QTRT1 Ensembl:ENSG00000213339 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10701476..10701625 26863410 MeRIP-seq:(Medium) rs747033386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512458,Human_RBP_ID_4558077,Human_RBP_ID_18420851,Human_RBP_ID_18721713 RMVar_hsa_circ_192422,RMVar_hsa_circ_107548 81676 RMVar_ID_81676 Human_SNP_ID_658279730 m1A Human chr19 - 10701716 10701716 10701716 GCCTCGCCGCCTCGCCGCCTCCCCGCGCGGGCAGAGCCCACCCACCGGCCTTAGACCCAGATGGT GCCTCGCCGCCTCGCCGCCTCCCCGCGCGGGCGGAGCCCACCCACCGGCCTTAGACCCAGATGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10701715..10701805 26863196 MeRIP-seq:(Medium) rs1193531207 Functional Loss SNV dbSNP153 33..33 33 - - - 81677 RMVar_ID_81677 Human_SNP_ID_658284673 m1A Human chr19 - 10718128 10718127 10718128 GCCGTTGCTCCCCGCCCGCCCGGGCCTCGGCAAGACGCCCGCTCCCGGCTCGGCCTCACGGTCGC GCCGTTGCTCCCCGCCCGCCCGGGCCTCGGCA_GACGCCCGCTCCCGGCTCGGCCTCACGGTCGC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr19:10718029..10718432;chr19:10718076..10718325 26863196 MeRIP-seq:(Medium) rs769214070 Functional Loss DEL dbSNP153 33..33 33 - - - 81678 RMVar_ID_81678 Human_SNP_ID_658296231 m1A Human chr19 + 10759740 10759740 10759740 GTAATTTCTGTCCCTCTCCCCCCCTCACAGGGACTTCCTTCCCCGCGGTTCAGGAATCGTCACCC GTAATTTCTGTCCCTCTCCCCCCCTCACAGGGGCTTCCTTCCCCGCGGTTCAGGAATCGTCACCC A G DNM2 Ensembl:ENSG00000079805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10759726..10759750 26863196 MeRIP-seq:(Medium) rs587778234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912612,Human_RBP_ID_3954461,Human_RBP_ID_4559224,Human_RBP_ID_18996578 Human_Splice_Rec_1956230,Human_Splice_Rec_1956231,Human_Splice_Rec_1956268,Human_Splice_Rec_1956269,Human_Splice_Rec_1956306,Human_Splice_Rec_1956307,Human_Splice_Rec_1956342,Human_Splice_Rec_1956343,Human_Splice_Rec_1956380,Human_Splice_Rec_1956381,Human_Splice_Rec_1956416,Human_Splice_Rec_1956417 Human_miRNA_ID_1971621 RMVar_hsa_circ_36659,RMVar_hsa_circ_105373,RMVar_hsa_circ_318285,RMVar_hsa_circ_371966,RMVar_hsa_circ_192432,RMVar_hsa_circ_328562,RMVar_hsa_circ_109643,RMVar_hsa_circ_192433,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_192434 81679 RMVar_ID_81679 Human_SNP_ID_658303922 m1A Human chr19 + 10788246 10788246 10788246 CAGAGTAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGAAGTTGAGTGTCAGGCGAAGACCTGA CAGAGTAAGACTCCGTCTCAAAAAAAAAAAAAGAAAAAGAAGTTGAGTGTCAGGCGAAGACCTGA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10788244..10788629 26863196 MeRIP-seq:(Medium) rs796735758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27757,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_61297,RMVar_hsa_circ_124037,RMVar_hsa_circ_26942,RMVar_hsa_circ_102345,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419,RMVar_hsa_circ_80209,RMVar_hsa_circ_192443,RMVar_hsa_circ_192444 81680 RMVar_ID_81680 Human_SNP_ID_658310091 m1A Human chr19 + 10811891 10811891 10811891 CACCTTTGACCCTAGCCCTCTGTGTGGATGCTACCCTTGGAACCTTATCTCACGCAAACAAGTGC CACCTTTGACCCTAGCCCTCTGTGTGGATGCTCCCCTTGGAACCTTATCTCACGCAAACAAGTGC A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10811889..10811990 32194978 MeRIP-seq:(Medium) rs1442987331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8476551,Human_RBP_ID_13361898,Human_RBP_ID_17082332,Human_RBP_ID_18721818,Human_RBP_ID_20432748,Human_RBP_ID_23781353 RMVar_hsa_circ_368856,RMVar_hsa_circ_10050,RMVar_hsa_circ_124037,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419,RMVar_hsa_circ_80209,RMVar_hsa_circ_328947,RMVar_hsa_circ_27079,RMVar_hsa_circ_192444,RMVar_hsa_circ_358374,RMVar_hsa_circ_14402,RMVar_hsa_circ_192450,RMVar_hsa_circ_17606,RMVar_hsa_circ_357431,RMVar_hsa_circ_107615,RMVar_hsa_circ_192453,RMVar_hsa_circ_287344 81681 RMVar_ID_81681 Human_SNP_ID_658312266 m1A Human chr19 + 10819703 10819703 10819703 GGTGGGGAGGGTGCGGGTAGAGTTAGGGCAGGAGGGAGCCATGCAAGTGTCAGGATCAGGCAGTA GGTGGGGAGGGTGCGGGTAGAGTTAGGGCAGGCGGGAGCCATGCAAGTGTCAGGATCAGGCAGTA A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10819700..10819826 26863196 MeRIP-seq:(Medium) rs1009412417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823867,Human_RBP_ID_3587902,Human_RBP_ID_5238647,Human_RBP_ID_5321426,Human_RBP_ID_9929711,Human_RBP_ID_22664863 RMVar_hsa_circ_10050,RMVar_hsa_circ_124037,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419,RMVar_hsa_circ_80209,RMVar_hsa_circ_192444,RMVar_hsa_circ_358374,RMVar_hsa_circ_192450,RMVar_hsa_circ_357431,RMVar_hsa_circ_107615,RMVar_hsa_circ_26526,RMVar_hsa_circ_192453,RMVar_hsa_circ_287344,RMVar_hsa_circ_346145 81682 RMVar_ID_81682 Human_SNP_ID_658313745 m1A Human chr19 + 10825107 10825107 10825107 GCCCAGGAGAACACCTTCTCCATGGACCCCCAACTGGAGCGGCAGGTGGAGACCATTCGCAACCT GCCCAGGAGAACACCTTCTCCATGGACCCCCAGCTGGAGCGGCAGGTGGAGACCATTCGCAACCT A G DNM2 Ensembl:ENSG00000079805 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10824774..10825125 32194978 MeRIP-seq:(Medium) rs541331101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910600,Human_RBP_ID_3956309,Human_RBP_ID_9381997,Human_RBP_ID_18191949,Human_RBP_ID_22446425,Human_RBP_ID_26815262 Human_Splice_Rec_1956260,Human_Splice_Rec_1956298,Human_Splice_Rec_1956334,Human_Splice_Rec_1956372,Human_Splice_Rec_1956408,Human_Splice_Rec_1956478,Human_Splice_Rec_1956490 Human_miRNA_ID_2071429,Human_miRNA_ID_2804355 RMVar_hsa_circ_80209,RMVar_hsa_circ_192444,RMVar_hsa_circ_358374,RMVar_hsa_circ_192450,RMVar_hsa_circ_107615,RMVar_hsa_circ_26526,RMVar_hsa_circ_339417,RMVar_hsa_circ_192455,RMVar_hsa_circ_335545 81683 RMVar_ID_81683 Human_SNP_ID_658314882 m1A Human chr19 + 10829150 10829150 10829150 ACCAGGCACAGCGGCGGGACGACATGCTGCGCATGTACCATGCCCTCAAGGAGGCGCTCAACATC ACCAGGCACAGCGGCGGGACGACATGCTGCGCGTGTACCATGCCCTCAAGGAGGCGCTCAACATC A G DNM2 Ensembl:ENSG00000079805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10829100..10829304 26863196 MeRIP-seq:(Medium) rs757876109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22809037 Human_miRNA_ID_2493940,Human_miRNA_ID_2696240 RMVar_hsa_circ_80209,RMVar_hsa_circ_192444,RMVar_hsa_circ_52653 81684 RMVar_ID_81684 Human_SNP_ID_658315219 m1A Human chr19 - 10830246 10830243 10830246 GTCCAGGCCGGGATGGGATTGGGGGCGCCGAGAAGGAGGCTGCTGCCCCCACGGGAACAGGAATC GTCCAGGCCGGGATGGGATTGGGGGCGCCGAG___GAGGCTGCTGCCCCCACGGGAACAGGAATC CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10830195..10830446 32194978 MeRIP-seq:(Medium) rs752014734 Functional Loss DEL dbSNP153,HGVD 33..35 33 - - - Clinvar_Rec_387 81685 RMVar_ID_81685 Human_SNP_ID_658315221 m1A Human chr19 - 10830246 10830246 10830246 GTCCAGGCCGGGATGGGATTGGGGGCGCCGAGAAGGAGGCTGCTGCCCCCACGGGAACAGGAATC GTCCAGGCCGGGATGGGATTGGGGGCGCCGAGGAGGAGGCTGCTGCCCCCACGGGAACAGGAATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10830195..10830446 32194978 MeRIP-seq:(Medium) rs1237677745 Functional Loss SNV dbSNP153 33..33 33 - - - 81686 RMVar_ID_81686 Human_SNP_ID_658315675 m1A Human chr19 - 10831522 10831522 10831522 TACACCTCAGGCCTGCCAGCTGGGCACTACCGAGCCCACTGGGCCAGGCTTGCCGCTGGGGAGCT TACACCTCAGGCCTGCCAGCTGGGCACTACCGGGCCCACTGGGCCAGGCTTGCCGCTGGGGAGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10831338..10831639 32194978 MeRIP-seq:(Medium) rs1391451362 Functional Loss SNV dbSNP153 33..33 33 - - - 81687 RMVar_ID_81687 Human_SNP_ID_658317345 m1A Human chr19 + 10836163 10836163 10836163 CCTCCACTGGTGGCATTAGTAGCCACAAGGCCAGGGCTAGGGCCGCGCCGGCCGCCATCATCCGG CCTCCACTGGTGGCATTAGTAGCCACAAGGCCCGGGCTAGGGCCGCGCCGGCCGCCATCATCCGG A C lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10835923..10836274 26863196 MeRIP-seq:(Medium) rs745361829 Functional Loss SNV dbSNP153 33..33 33 - - - 81688 RMVar_ID_81688 Human_SNP_ID_658327702 m1A Human chr19 + 10871640 10871595 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG _________________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1160698945 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81689 RMVar_ID_81689 Human_SNP_ID_658327706 m1A Human chr19 + 10871640 10871598 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG _________________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1369686087 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81690 RMVar_ID_81690 Human_SNP_ID_658327713 m1A Human chr19 + 10871640 10871601 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG _________________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1358472215 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81691 RMVar_ID_81691 Human_SNP_ID_658327725 m1A Human chr19 + 10871640 10871604 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG _________________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1394893680 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81692 RMVar_ID_81692 Human_SNP_ID_658327733 m1A Human chr19 + 10871640 10871607 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG _________________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1267913323 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81693 RMVar_ID_81693 Human_SNP_ID_658327741 m1A Human chr19 + 10871640 10871610 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCG______________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1284178626 Functional Loss DEL dbSNP153 4..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81694 RMVar_ID_81694 Human_SNP_ID_658327756 m1A Human chr19 + 10871640 10871613 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCG___________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1428098239 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81695 RMVar_ID_81695 Human_SNP_ID_658327760 m1A Human chr19 + 10871640 10871616 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCG________________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1458207713 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81696 RMVar_ID_81696 Human_SNP_ID_658327767 m1A Human chr19 + 10871640 10871619 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCG_____________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1279547578 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81697 RMVar_ID_81697 Human_SNP_ID_658327773 m1A Human chr19 + 10871640 10871622 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCG__________________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1448162890 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81698 RMVar_ID_81698 Human_SNP_ID_658327776 m1A Human chr19 + 10871640 10871625 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCG_______________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1415856406 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81699 RMVar_ID_81699 Human_SNP_ID_658327780 m1A Human chr19 + 10871666 10871625 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC _________________________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1568342811 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81700 RMVar_ID_81700 Human_SNP_ID_658327784 m1A Human chr19 + 10871640 10871628 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCG____________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1418288852 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81701 RMVar_ID_81701 Human_SNP_ID_658327794 m1A Human chr19 + 10871666 10871631 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC _________________________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1356303549 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81702 RMVar_ID_81702 Human_SNP_ID_658327795 m1A Human chr19 + 10871640 10871631 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCG_________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1241260466 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81703 RMVar_ID_81703 Human_SNP_ID_658327799 m1A Human chr19 + 10871666 10871634 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC G________________________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1302985188 Functional Loss DEL dbSNP153 2..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81704 RMVar_ID_81704 Human_SNP_ID_658327802 m1A Human chr19 + 10871640 10871634 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCG______GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1377767001 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81705 RMVar_ID_81705 Human_SNP_ID_658327806 m1A Human chr19 + 10871666 10871637 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCG_____________________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCAGCGGCGGCGGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1414623932 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81706 RMVar_ID_81706 Human_SNP_ID_658327812 m1A Human chr19 + 10871640 10871637 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCG___GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1555723477 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81707 RMVar_ID_81707 Human_SNP_ID_658327818 m1A Human chr19 + 10871640 10871640 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG A G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs866968375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81708 RMVar_ID_81708 Human_SNP_ID_658327819 m1A Human chr19 + 10871640 10871640 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG A T CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs866968375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81709 RMVar_ID_81709 Human_SNP_ID_658327826 m1A Human chr19 + 10871666 10871643 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCAGCG_______________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCGGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1362184001 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81710 RMVar_ID_81710 Human_SNP_ID_658327835 m1A Human chr19 + 10871666 10871649 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCAGCGGCGGCG_________________GCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCCTGGGCCCGGGCGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1350342041 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81711 RMVar_ID_81711 Human_SNP_ID_658327848 m1A Human chr19 + 10871666 10871666 10871666 GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC GGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCGGCGGCGGCGGCGGCGGGGCCTGGAGCCGGATC A G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10871626..10871900 26863196 MeRIP-seq:(Medium) rs1222134520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81712 RMVar_ID_81712 Human_SNP_ID_658327863 m1A Human chr19 - 10871687 10871687 10871687 GCCGCCGCCGCTGCCATCTTAGATCCGGCTCCAGGCCCCGCCGCCGCCGCCGCTGCGCCCGGGCC GCCGCCGCCGCTGCCATCTTAGATCCGGCTCCGGGCCCCGCCGCCGCCGCCGCTGCGCCCGGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr19:10871494..10905000;chr19:10871503..10871792 26863196,26863410 MeRIP-seq:(Medium) rs1460452258 Functional Loss SNV dbSNP153 33..33 33 - - - 81713 RMVar_ID_81713 Human_SNP_ID_658327867 m1A Human chr19 + 10871708 10871705 10871708 GCGGCGGGGCCTGGAGCCGGATCTAAGATGGCAGCGGCGGCGGCGGCGGTGGGGCCGGGCGCGGG GCGGCGGGGCCTGGAGCCGGATCTAAGATG___GCGGCGGCGGCGGCGGTGGGGCCGGGCGCGGG GGCA G CARM1 Ensembl:ENSG00000142453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10871657..10871847 26863196 MeRIP-seq:(Medium) rs1467257049 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81714 RMVar_ID_81714 Human_SNP_ID_658327868 m1A Human chr19 + 10871708 10871708 10871708 GCGGCGGGGCCTGGAGCCGGATCTAAGATGGCAGCGGCGGCGGCGGCGGTGGGGCCGGGCGCGGG GCGGCGGGGCCTGGAGCCGGATCTAAGATGGCGGCGGCGGCGGCGGCGGTGGGGCCGGGCGCGGG A G CARM1 Ensembl:ENSG00000142453 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10871657..10871847 26863196 MeRIP-seq:(Medium) rs1434074365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140280,Human_RBP_ID_4557219 81715 RMVar_ID_81715 Human_SNP_ID_658327875 m1A Human chr19 - 10871725 10871725 10871725 CCGCCGACCCCGCGCCGCCCGCGCCCGGCCCCACCGCCGCCGCCGCCGCTGCCATCTTAGATCCG CCGCCGACCCCGCGCCGCCCGCGCCCGGCCCCCCCGCCGCCGCCGCCGCTGCCATCTTAGATCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10871626..10872188;chr19:10871601..10872235 26863196 MeRIP-seq:(Medium) rs539895704 Functional Loss SNV dbSNP153 33..33 33 - - - 81716 RMVar_ID_81716 Human_SNP_ID_658327888 m1A Human chr19 - 10871751 10871751 10871751 AGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGACCCCGCGCCGCCCGCGCCCGGCCCCACCGCCG AGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGGCCCCGCGCCGCCCGCGCCCGGCCCCACCGCCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:10871615..10871850 26863410 MeRIP-seq:(Medium) rs1046965708 Functional Loss SNV dbSNP153 33..33 33 - - - 81717 RMVar_ID_81717 Human_SNP_ID_658327889 m1A Human chr19 - 10871751 10871751 10871751 AGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGACCCCGCGCCGCCCGCGCCCGGCCCCACCGCCG AGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGCCCCCGCGCCGCCCGCGCCCGGCCCCACCGCCG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:10871615..10871850 26863410 MeRIP-seq:(Medium) rs1046965708 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 81718 RMVar_ID_81718 Human_SNP_ID_658327902 m1A Human chr19 - 10871783 10871783 10871783 AGGAGGCGGGCGCCGGGGAACACCGACACGGTAGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGA AGGAGGCGGGCGCCGGGGAACACCGACACGGTCGCGCAGGGCCCCGCGCCGCCCGGGACCGCCGA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10871637..10871925 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81719 RMVar_ID_81719 Human_SNP_ID_658334873 m1A Human chr19 - 10896005 10896005 10896005 ATGTCTGCAGTCTCACTGCTGCCCCCTGGGTCACTCCAGCCAAACCTCGCTGGCCTTCAACACTC ATGTCTGCAGTCTCACTGCTGCCCCCTGGGTCGCTCCAGCCAAACCTCGCTGGCCTTCAACACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10896002..10896115 26863196 MeRIP-seq:(Medium) rs1568350258 Functional Loss SNV dbSNP153 33..33 33 - - - 81720 RMVar_ID_81720 Human_SNP_ID_658342006 m1A Human chr19 - 10921720 10921720 10921720 TCCCGTAGTGCATGGTGTTGGTCGGGATGGACATGGGCGACGCCATGGAGATGGCGGGGCCGCCC TCCCGTAGTGCATGGTGTTGGTCGGGATGGACGTGGGCGACGCCATGGAGATGGCGGGGCCGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10921670..10922092 26863196 MeRIP-seq:(Medium) rs1240301666 Functional Loss SNV dbSNP153 33..33 33 - - - 81721 RMVar_ID_81721 Human_SNP_ID_658342088 m1A Human chr19 - 10921897 10921896 10921898 AGGGTGGGGACGGCGGCAACATCGTGTAAAAAAGTGTCCCAGTTCCCATAGCAAAGAGAGCTGTG AGGGTGGGGACGGCGGCAACATCGTGTAAAA__GTGTCCCAGTTCCCATAGCAAAGAGAGCTGTG CTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10921602..10922085 26863196 MeRIP-seq:(Medium) rs1412063774 Functional Loss DEL dbSNP153 32..33 33 - - - 81722 RMVar_ID_81722 Human_SNP_ID_658342089 m1A Human chr19 - 10921897 10921897 10921897 AGGGTGGGGACGGCGGCAACATCGTGTAAAAAAGTGTCCCAGTTCCCATAGCAAAGAGAGCTGTG AGGGTGGGGACGGCGGCAACATCGTGTAAAAAGGTGTCCCAGTTCCCATAGCAAAGAGAGCTGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10921602..10922085 26863196 MeRIP-seq:(Medium) rs780832255 Functional Loss SNV dbSNP153 33..33 33 - - - 81723 RMVar_ID_81723 Human_SNP_ID_658342350 m1A Human chr19 - 10922598 10922598 10922598 TGGAGGGGAGCTACTCAGGCCTAACGTTAGCTACAAGGAAAAAGGACGCCTTCCGTGACAGATCC TGGAGGGGAGCTACTCAGGCCTAACGTTAGCTGCAAGGAAAAAGGACGCCTTCCGTGACAGATCC T C YIPF2 Ensembl:ENSG00000130733 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10922547..10922641 26863196 MeRIP-seq:(Medium) rs980506379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512626,Human_RBP_ID_3562565,Human_RBP_ID_4499762,Human_RBP_ID_6718201,Human_RBP_ID_13362975,Human_RBP_ID_22966570 81724 RMVar_ID_81724 Human_SNP_ID_658342351 m1A Human chr19 - 10922602 10922602 10922602 AGGATGGAGGGGAGCTACTCAGGCCTAACGTTAGCTACAAGGAAAAAGGACGCCTTCCGTGACAG AGGATGGAGGGGAGCTACTCAGGCCTAACGTTCGCTACAAGGAAAAAGGACGCCTTCCGTGACAG T G YIPF2 Ensembl:ENSG00000130733 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10922551..10922942 26863196 MeRIP-seq:(Medium) rs1225827621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512626,Human_RBP_ID_3562565,Human_RBP_ID_6718201,Human_RBP_ID_13362975,Human_RBP_ID_22966570 81725 RMVar_ID_81725 Human_SNP_ID_658342394 m1A Human chr19 + 10922744 10922743 10922745 CTCCCTCCAAAAAAAGAAAAAAAGAAAAAGAAAGAAAAAATAAATGAGGAAACGTGTTGCAGCAC CTCCCTCCAAAAAAAGAAAAAAAGAAAAAGAA__AAAAAATAAATGAGGAAACGTGTTGCAGCAC AAG A CARM1 Ensembl:ENSG00000142453 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10922694..10922788 26863196 MeRIP-seq:(Medium) rs1428010320 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_512634,Human_RBP_ID_18721895,Human_RBP_ID_26464196 81726 RMVar_ID_81726 Human_SNP_ID_658344517 m1A Human chr19 - 10928850 10928850 10928850 CGCGTCGCCCGCCTCTGCGCGGCGCCGGGACCAAAATCTCCTCAGAGCCGCCGCGGCCATCCTCT CGCGTCGCCCGCCTCTGCGCGGCGCCGGGACCTAAATCTCCTCAGAGCCGCCGCGGCCATCCTCT T A RF00017-1792 RNACentral:URS000096ECA5 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10928801..10929100;chr19:10928801..10929693;chr19:10928801..10929223 26863196 MeRIP-seq:(Medium) rs1042224448 Functional Loss SNV dbSNP153 33..33 33 - - - 81727 RMVar_ID_81727 Human_SNP_ID_658344518 m1A Human chr19 - 10928853 10928853 10928853 TACCGCGTCGCCCGCCTCTGCGCGGCGCCGGGACCAAAATCTCCTCAGAGCCGCCGCGGCCATCC TACCGCGTCGCCCGCCTCTGCGCGGCGCCGGGCCCAAAATCTCCTCAGAGCCGCCGCGGCCATCC T G RF00017-1792 RNACentral:URS000096ECA5 SRP RNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr19:10928801..10929122;chr19:10928776..10929337 26863196 MeRIP-seq:(Medium) rs778883903 Functional Loss SNV dbSNP153 33..33 33 - - - 81728 RMVar_ID_81728 Human_SNP_ID_658344647 m1A Human chr19 - 10929119 10929119 10929119 GCGCCAGCGTGAAGCAGGCCGCCGCGCCGCCCAGCAGACCCACATACACAGCGGCGCGCCCCGGC GCGCCAGCGTGAAGCAGGCCGCCGCGCCGCCCGGCAGACCCACATACACAGCGGCGCGCCCCGGC T C RF00017-1792 RNACentral:URS000096ECA5 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10928925..10929195 26863196 MeRIP-seq:(Medium) rs1440941688 Functional Loss SNV dbSNP153 33..33 33 - - - 81729 RMVar_ID_81729 Human_SNP_ID_658344698 m1A Human chr19 + 10929226 10929226 10929226 GGACCCTCCTGCTGCTGGCGCCGGCCACCCGCAACCGCGAGTCCGAAGCCTTCGTGCAGAGGCTG GGACCCTCCTGCTGCTGGCGCCGGCCACCCGCCACCGCGAGTCCGAAGCCTTCGTGCAGAGGCTG A C TIMM29 Ensembl:ENSG00000142444 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10929124..10929321 26863410 MeRIP-seq:(Medium) rs1433534410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22447382 81730 RMVar_ID_81730 Human_SNP_ID_658344802 m1A Human chr19 - 10929429 10929421 10929430 TCGCGCATCCAGGCCCCCAGCACCCACCAGCGACCCACGAAGCCCACGTCCAGGACCCGGCCGGG TCGCGCATCCAGGCCCCCAGCACCCACCAGC_________AGCCCACGTCCAGGACCCGGCCGGG TTCGTGGGTC T RF00017-1792 RNACentral:URS000096ECA5 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10929124..10929864 32194978 MeRIP-seq:(Medium) rs770577761 Functional Loss DEL dbSNP153 32..40 33 - - - 81731 RMVar_ID_81731 Human_SNP_ID_658344912 m1A Human chr19 + 10929605 10929605 10929605 GCCTGTCGTGCTCACCGACGATCAGGTGGACCAGGCGCTGTGGGAGGAGCAGGTCTTGCAGAAGG GCCTGTCGTGCTCACCGACGATCAGGTGGACCTGGCGCTGTGGGAGGAGCAGGTCTTGCAGAAGG A T TIMM29 Ensembl:ENSG00000142444 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10929557..10929698 26863196 MeRIP-seq:(Medium) rs763538420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241698,Human_RBP_ID_23119169,Human_RBP_ID_26335672 81732 RMVar_ID_81732 Human_SNP_ID_658353941 m1A Human chr19 + 10960590 10960590 10960590 CCAGGCGGCCCGTCCTACGGTCCAGGGTTCCTATTTCCGAGCCTCAGGGACCTCCTTTCCCCACG CCAGGCGGCCCGTCCTACGGTCCAGGGTTCCTGTTTCCGAGCCTCAGGGACCTCCTTTCCCCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10960587..10960658 26863196 MeRIP-seq:(Medium) rs552120651 Functional Loss SNV dbSNP153 33..33 33 - - - 81733 RMVar_ID_81733 Human_SNP_ID_658354212 m1A Human chr19 - 10961077 10961073 10961077 GAATGGGCGTCTCGCTTCTCTTCACGAAACAAAGAAGCCGCCGCCGCCGCCAAACGAGGGGAAGC GAATGGGCGTCTCGCTTCTCTTCACGAAACAA____GCCGCCGCCGCCGCCAAACGAGGGGAAGC CTTCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10961026..10961259 26863196 MeRIP-seq:(Medium) rs1302940605 Functional Loss DEL dbSNP153 33..36 33 - - - 81734 RMVar_ID_81734 Human_SNP_ID_658354213 m1A Human chr19 - 10961077 10961077 10961077 GAATGGGCGTCTCGCTTCTCTTCACGAAACAAAGAAGCCGCCGCCGCCGCCAAACGAGGGGAAGC GAATGGGCGTCTCGCTTCTCTTCACGAAACAATGAAGCCGCCGCCGCCGCCAAACGAGGGGAAGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:10961026..10961259 26863196 MeRIP-seq:(Medium) rs1236013624 Functional Loss SNV dbSNP153 33..33 33 - - - 81735 RMVar_ID_81735 Human_SNP_ID_658354216 m1A Human chr19 + 10961100 10961100 10961100 GGCGGCTTCTTTGTTTCGTGAAGAGAAGCGAGACGCCCATTCTGCCCCCGGCCCCGCGCGGAGGG GGCGGCTTCTTTGTTTCGTGAAGAGAAGCGAGGCGCCCATTCTGCCCCCGGCCCCGCGCGGAGGG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:10961001..10961222 26863196 MeRIP-seq:(Medium) rs942228160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4499976,Human_RBP_ID_5442652,Human_RBP_ID_9293389,Human_RBP_ID_17914565,Human_RBP_ID_22069717 Human_Splice_Rec_1956865,Human_Splice_Rec_1956933,Human_Splice_Rec_1956999,Human_Splice_Rec_1957069,Human_Splice_Rec_1957137,Human_Splice_Rec_1957203,Human_Splice_Rec_1957267,Human_Splice_Rec_1957335,Human_Splice_Rec_1957399,Human_Splice_Rec_1957465,Human_Splice_Rec_1957533,Human_Splice_Rec_1957603,Human_Splice_Rec_1957611,Human_Splice_Rec_1957677,Human_Splice_Rec_1957743,Human_Splice_Rec_1957809 81736 RMVar_ID_81736 Human_SNP_ID_658354217 m1A Human chr19 + 10961100 10961100 10961100 GGCGGCTTCTTTGTTTCGTGAAGAGAAGCGAGACGCCCATTCTGCCCCCGGCCCCGCGCGGAGGG GGCGGCTTCTTTGTTTCGTGAAGAGAAGCGAGTCGCCCATTCTGCCCCCGGCCCCGCGCGGAGGG A T SMARCA4 Ensembl:ENSG00000127616 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:10961001..10961222 26863196 MeRIP-seq:(Medium) rs942228160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4499976,Human_RBP_ID_5442652,Human_RBP_ID_9293389,Human_RBP_ID_17914565,Human_RBP_ID_22069717 Human_Splice_Rec_1956865,Human_Splice_Rec_1956933,Human_Splice_Rec_1956999,Human_Splice_Rec_1957069,Human_Splice_Rec_1957137,Human_Splice_Rec_1957203,Human_Splice_Rec_1957267,Human_Splice_Rec_1957335,Human_Splice_Rec_1957399,Human_Splice_Rec_1957465,Human_Splice_Rec_1957533,Human_Splice_Rec_1957603,Human_Splice_Rec_1957611,Human_Splice_Rec_1957677,Human_Splice_Rec_1957743,Human_Splice_Rec_1957809 81737 RMVar_ID_81737 Human_SNP_ID_658361241 m1A Human chr19 + 10985350 10985349 10985351 TACAACCAGATGAAAGGAATGGGGATGCGGTCAGGGGGCCATGCTGGGATGGGGCCCCCGCCCAG TACAACCAGATGAAAGGAATGGGGATGCGGTC__GGGGCCATGCTGGGATGGGGCCCCCGCCCAG CAG C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10985301..10985440 26863196 MeRIP-seq:(Medium) rs780424104 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_55249,Human_RBP_ID_1012895,Human_RBP_ID_6718310,Human_RBP_ID_8829419,Human_RBP_ID_9293391,Human_RBP_ID_17655516,Human_RBP_ID_18470495 Human_Splice_Rec_1956868,Human_Splice_Rec_1956869,Human_Splice_Rec_1956936,Human_Splice_Rec_1956937,Human_Splice_Rec_1957002,Human_Splice_Rec_1957003,Human_Splice_Rec_1957072,Human_Splice_Rec_1957073,Human_Splice_Rec_1957140,Human_Splice_Rec_1957141,Human_Splice_Rec_1957206,Human_Splice_Rec_1957207,Human_Splice_Rec_1957270,Human_Splice_Rec_1957271,Human_Splice_Rec_1957338,Human_Splice_Rec_1957339,Human_Splice_Rec_1957402,Human_Splice_Rec_1957403,Human_Splice_Rec_1957470,Human_Splice_Rec_1957471,Human_Splice_Rec_1957538,Human_Splice_Rec_1957539,Human_Splice_Rec_1957608,Human_Splice_Rec_1957609,Human_Splice_Rec_1957614,Human_Splice_Rec_1957615,Human_Splice_Rec_1957682,Human_Splice_Rec_1957683,Human_Splice_Rec_1957748,Human_Splice_Rec_1957749,Human_Splice_Rec_1957814,Human_Splice_Rec_1957815,Human_Splice_Rec_1957880,Human_Splice_Rec_1957881,Human_Splice_Rec_1957944,Human_Splice_Rec_1957945,Human_Splice_Rec_1958008,Human_Splice_Rec_1958009,Human_Splice_Rec_1958076,Human_Splice_Rec_1958077 Clinvar_Rec_388 RMVar_hsa_circ_53263,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_192479,RMVar_hsa_circ_51785,RMVar_hsa_circ_192480 81738 RMVar_ID_81738 Human_SNP_ID_658361696 m1A Human chr19 - 10986556 10986544 10986556 GGCCTGCTGTAATTTGGAGGTGCCGGGCCGGGACCCGGGCCGGGGCCAGGGCCAGGGCCAGGGCC GGCCTGCTGTAATTTGGAGGTGCCGGGCCGGG____________GCCAGGGCCAGGGCCAGGGCC CCCCGGCCCGGGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:10986401..10986653 26863196 MeRIP-seq:(Medium) rs568390760 Functional Loss DEL dbSNP153 33..44 33 - - - Clinvar_Rec_389 81739 RMVar_ID_81739 Human_SNP_ID_658361722 m1A Human chr19 - 10986578 10986578 10986578 AGGGCAGCCAGTCTTACCATGAGGCCTGCTGTAATTTGGAGGTGCCGGGCCGGGACCCGGGCCGG AGGGCAGCCAGTCTTACCATGAGGCCTGCTGTTATTTGGAGGTGCCGGGCCGGGACCCGGGCCGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10984160..10995178 32194978 MeRIP-seq:(Medium) rs1314840008 Functional Loss SNV dbSNP153 33..33 33 - - - 81740 RMVar_ID_81740 Human_SNP_ID_658362106 m1A Human chr19 - 10987715 10987715 10987715 GCGGGGGAAGGGCGGCCCGTTGGCTGCGGGGGAATCAGCTTCTGAGGGGTGCTCGTGGGGGCAGC GCGGGGGAAGGGCGGCCCGTTGGCTGCGGGGGCATCAGCTTCTGAGGGGTGCTCGTGGGGGCAGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:10987570..10987858;chr19:10987602..10987900;chr19:10987584..10987925 26863196 MeRIP-seq:(Medium) rs1555754852 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_390 81741 RMVar_ID_81741 Human_SNP_ID_658362170 m1A Human chr19 + 10987787 10987787 10987787 GCCGTCCCACCCGCCGCCTCGCCCGTGATGCCACCGCAGACCCAGTCCCCCGGGCAGCCGGCCCA GCCGTCCCACCCGCCGCCTCGCCCGTGATGCCCCCGCAGACCCAGTCCCCCGGGCAGCCGGCCCA A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10987651..10987841 26863196 MeRIP-seq:(Medium) rs547268941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9382001,Human_RBP_ID_18945050 Clinvar_Rec_391 RMVar_hsa_circ_53263,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_51785 81742 RMVar_ID_81742 Human_SNP_ID_658362173 m1A Human chr19 + 10987792 10987792 10987792 CCCACCCGCCGCCTCGCCCGTGATGCCACCGCAGACCCAGTCCCCCGGGCAGCCGGCCCAGCCCG CCCACCCGCCGCCTCGCCCGTGATGCCACCGCGGACCCAGTCCCCCGGGCAGCCGGCCCAGCCCG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10987615..10987900 26863410 MeRIP-seq:(Medium) rs775843321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9382001,Human_RBP_ID_18945050 Clinvar_Rec_392 RMVar_hsa_circ_53263,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_51785 81743 RMVar_ID_81743 Human_SNP_ID_658364314 m1A Human chr19 + 10994972 10994972 10994972 CGGAGCGGGAGCAGAAGAAAGAGAACGAGCGGATCGAGAAGGAGCGCATGCGGAGGCTCATGGTA CGGAGCGGGAGCAGAAGAAAGAGAACGAGCGGGTCGAGAAGGAGCGCATGCGGAGGCTCATGGTA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10994901..10995056 26863196 MeRIP-seq:(Medium) rs1568440731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_204489,Human_RBP_ID_240111,Human_RBP_ID_3956320,Human_RBP_ID_9380484,Human_RBP_ID_13363592,Human_RBP_ID_24545711,Human_RBP_ID_26335680 Human_Splice_Rec_1956881,Human_Splice_Rec_1956949,Human_Splice_Rec_1957015,Human_Splice_Rec_1957085,Human_Splice_Rec_1957153,Human_Splice_Rec_1957219,Human_Splice_Rec_1957283,Human_Splice_Rec_1957351,Human_Splice_Rec_1957415,Human_Splice_Rec_1957483,Human_Splice_Rec_1957551,Human_Splice_Rec_1957627,Human_Splice_Rec_1957695,Human_Splice_Rec_1957761,Human_Splice_Rec_1957827,Human_Splice_Rec_1957893,Human_Splice_Rec_1958021,Human_Splice_Rec_1958089,Human_Splice_Rec_1958131,Human_Splice_Rec_1958185,Human_Splice_Rec_1958239,Human_Splice_Rec_1958289,Human_Splice_Rec_1958339,Human_Splice_Rec_1958391,Human_Splice_Rec_1958441,Human_Splice_Rec_1958495 Clinvar_Rec_393 RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_7395,RMVar_hsa_circ_51785,RMVar_hsa_circ_80212,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192481,RMVar_hsa_circ_304210,RMVar_hsa_circ_20169,RMVar_hsa_circ_192482 81744 RMVar_ID_81744 Human_SNP_ID_658364869 m1A Human chr19 + 10996502 10996502 10996502 GACCGTGTCTCTCTCTATTTCCAGAAGGCAGAAAATGCAGAAGGACAGACGCCTGCCATTGGGCC GACCGTGTCTCTCTCTATTTCCAGAAGGCAGAGAATGCAGAAGGACAGACGCCTGCCATTGGGCC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10996164..11003208 26863196 MeRIP-seq:(Medium) rs1555763953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53713,Human_RBP_ID_3956321,Human_RBP_ID_5375702,Human_RBP_ID_18996603 Human_Splice_Rec_1956884,Human_Splice_Rec_1956885,Human_Splice_Rec_1956952,Human_Splice_Rec_1956953,Human_Splice_Rec_1957018,Human_Splice_Rec_1957019,Human_Splice_Rec_1957088,Human_Splice_Rec_1957089,Human_Splice_Rec_1957156,Human_Splice_Rec_1957157,Human_Splice_Rec_1957222,Human_Splice_Rec_1957223,Human_Splice_Rec_1957286,Human_Splice_Rec_1957287,Human_Splice_Rec_1957354,Human_Splice_Rec_1957355,Human_Splice_Rec_1957418,Human_Splice_Rec_1957419,Human_Splice_Rec_1957486,Human_Splice_Rec_1957487,Human_Splice_Rec_1957554,Human_Splice_Rec_1957555,Human_Splice_Rec_1957630,Human_Splice_Rec_1957631,Human_Splice_Rec_1957698,Human_Splice_Rec_1957699,Human_Splice_Rec_1957764,Human_Splice_Rec_1957765,Human_Splice_Rec_1957830,Human_Splice_Rec_1957831,Human_Splice_Rec_1957896,Human_Splice_Rec_1957897,Human_Splice_Rec_1957962,Human_Splice_Rec_1957963,Human_Splice_Rec_1958024,Human_Splice_Rec_1958025,Human_Splice_Rec_1958092,Human_Splice_Rec_1958093,Human_Splice_Rec_1958134,Human_Splice_Rec_1958135,Human_Splice_Rec_1958188,Human_Splice_Rec_1958189,Human_Splice_Rec_1958242,Human_Splice_Rec_1958243,Human_Splice_Rec_1958292,Human_Splice_Rec_1958293,Human_Splice_Rec_1958342,Human_Splice_Rec_1958343,Human_Splice_Rec_1958394,Human_Splice_Rec_1958395,Human_Splice_Rec_1958444,Human_Splice_Rec_1958445,Human_Splice_Rec_1958498,Human_Splice_Rec_1958499,Human_Splice_Rec_1958526,Human_Splice_Rec_1958527,Human_Splice_Rec_1958574,Human_Splice_Rec_1958575,Human_Splice_Rec_1958614,Human_Splice_Rec_1958615,Human_Splice_Rec_1958660,Human_Splice_Rec_1958661,Human_Splice_Rec_1958710,Human_Splice_Rec_1958711,Human_Splice_Rec_1958760,Human_Splice_Rec_1958761 Clinvar_Rec_394 RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_7395,RMVar_hsa_circ_51785,RMVar_hsa_circ_80212,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192481,RMVar_hsa_circ_304210,RMVar_hsa_circ_20169,RMVar_hsa_circ_192482 81745 RMVar_ID_81745 Human_SNP_ID_658366640 m1A Human chr19 - 11002975 11002975 11002975 GACACTGAGGTTGCAGGGCCTCCAGACCAAACACTTACAGAGGCCAAGGTGGGAAGCACCCACTC GACACTGAGGTTGCAGGGCCTCCAGACCAAACGCTTACAGAGGCCAAGGTGGGAAGCACCCACTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11002973..11003215 26863196 MeRIP-seq:(Medium) rs17001078 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_9608,GWAS_ID_9609,GWAS_ID_9610,GWAS_ID_9611,GWAS_ID_9612,GWAS_ID_9613,GWAS_ID_9614,GWAS_ID_9615,GWAS_ID_9616,GWAS_ID_9617 81746 RMVar_ID_81746 Human_SNP_ID_658366645 m1A Human chr19 - 11002993 11002990 11002993 AAAAAGAGTCATTCGTGTGACACTGAGGTTGCAGGGCCTCCAGACCAAACACTTACAGAGGCCAA AAAAAGAGTCATTCGTGTGACACTGAGGTTGC___GCCTCCAGACCAAACACTTACAGAGGCCAA CCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11002989..11003175 26863196 MeRIP-seq:(Medium) rs773048508 Functional Loss DEL dbSNP153 33..35 33 - - - 81747 RMVar_ID_81747 Human_SNP_ID_658366812 m1A Human chr19 + 11003390 11003390 11003390 GTCTGATAGTGAAGAAAGTGGCTCAGAAGAAGAGGAAGAGGTAAGAGTGCATTTCCTGGCTTTCA GTCTGATAGTGAAGAAAGTGGCTCAGAAGAAGCGGAAGAGGTAAGAGTGCATTTCCTGGCTTTCA A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:11003326..11003400 26863196 MeRIP-seq:(Medium) rs754483795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913042,Human_RBP_ID_8839108,Human_RBP_ID_9293403,Human_RBP_ID_9380490,Human_RBP_ID_24545435,Human_RBP_ID_26335685 Human_Splice_Rec_1956888,Human_Splice_Rec_1956889,Human_Splice_Rec_1956956,Human_Splice_Rec_1956957,Human_Splice_Rec_1957022,Human_Splice_Rec_1957023,Human_Splice_Rec_1957092,Human_Splice_Rec_1957093,Human_Splice_Rec_1957160,Human_Splice_Rec_1957161,Human_Splice_Rec_1957226,Human_Splice_Rec_1957227,Human_Splice_Rec_1957290,Human_Splice_Rec_1957291,Human_Splice_Rec_1957358,Human_Splice_Rec_1957359,Human_Splice_Rec_1957422,Human_Splice_Rec_1957423,Human_Splice_Rec_1957490,Human_Splice_Rec_1957491,Human_Splice_Rec_1957558,Human_Splice_Rec_1957559,Human_Splice_Rec_1957634,Human_Splice_Rec_1957635,Human_Splice_Rec_1957702,Human_Splice_Rec_1957703,Human_Splice_Rec_1957768,Human_Splice_Rec_1957769,Human_Splice_Rec_1957834,Human_Splice_Rec_1957835,Human_Splice_Rec_1957900,Human_Splice_Rec_1957901,Human_Splice_Rec_1957966,Human_Splice_Rec_1957967,Human_Splice_Rec_1958028,Human_Splice_Rec_1958029,Human_Splice_Rec_1958096,Human_Splice_Rec_1958097,Human_Splice_Rec_1958138,Human_Splice_Rec_1958139,Human_Splice_Rec_1958192,Human_Splice_Rec_1958193,Human_Splice_Rec_1958246,Human_Splice_Rec_1958247,Human_Splice_Rec_1958296,Human_Splice_Rec_1958297,Human_Splice_Rec_1958346,Human_Splice_Rec_1958347,Human_Splice_Rec_1958398,Human_Splice_Rec_1958399,Human_Splice_Rec_1958448,Human_Splice_Rec_1958449,Human_Splice_Rec_1958502,Human_Splice_Rec_1958503,Human_Splice_Rec_1958530,Human_Splice_Rec_1958531,Human_Splice_Rec_1958578,Human_Splice_Rec_1958579,Human_Splice_Rec_1958618,Human_Splice_Rec_1958619,Human_Splice_Rec_1958664,Human_Splice_Rec_1958665,Human_Splice_Rec_1958714,Human_Splice_Rec_1958715,Human_Splice_Rec_1958764,Human_Splice_Rec_1958765,Human_Splice_Rec_1958808,Human_Splice_Rec_1958809,Human_Splice_Rec_1958828,Human_Splice_Rec_1958829 Clinvar_Rec_395 RMVar_hsa_circ_2241,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_51785,RMVar_hsa_circ_80212,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192481,RMVar_hsa_circ_20169,RMVar_hsa_circ_283257,RMVar_hsa_circ_192482,RMVar_hsa_circ_21252,RMVar_hsa_circ_114765,RMVar_hsa_circ_192483,RMVar_hsa_circ_192484 81748 RMVar_ID_81748 Human_SNP_ID_658366813 m1A Human chr19 + 11003390 11003390 11003390 GTCTGATAGTGAAGAAAGTGGCTCAGAAGAAGAGGAAGAGGTAAGAGTGCATTTCCTGGCTTTCA GTCTGATAGTGAAGAAAGTGGCTCAGAAGAAGTGGAAGAGGTAAGAGTGCATTTCCTGGCTTTCA A T SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:11003326..11003400 26863196 MeRIP-seq:(Medium) rs754483795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913042,Human_RBP_ID_8839108,Human_RBP_ID_9293403,Human_RBP_ID_9380490,Human_RBP_ID_24545435,Human_RBP_ID_26335685 Human_Splice_Rec_1956888,Human_Splice_Rec_1956889,Human_Splice_Rec_1956956,Human_Splice_Rec_1956957,Human_Splice_Rec_1957022,Human_Splice_Rec_1957023,Human_Splice_Rec_1957092,Human_Splice_Rec_1957093,Human_Splice_Rec_1957160,Human_Splice_Rec_1957161,Human_Splice_Rec_1957226,Human_Splice_Rec_1957227,Human_Splice_Rec_1957290,Human_Splice_Rec_1957291,Human_Splice_Rec_1957358,Human_Splice_Rec_1957359,Human_Splice_Rec_1957422,Human_Splice_Rec_1957423,Human_Splice_Rec_1957490,Human_Splice_Rec_1957491,Human_Splice_Rec_1957558,Human_Splice_Rec_1957559,Human_Splice_Rec_1957634,Human_Splice_Rec_1957635,Human_Splice_Rec_1957702,Human_Splice_Rec_1957703,Human_Splice_Rec_1957768,Human_Splice_Rec_1957769,Human_Splice_Rec_1957834,Human_Splice_Rec_1957835,Human_Splice_Rec_1957900,Human_Splice_Rec_1957901,Human_Splice_Rec_1957966,Human_Splice_Rec_1957967,Human_Splice_Rec_1958028,Human_Splice_Rec_1958029,Human_Splice_Rec_1958096,Human_Splice_Rec_1958097,Human_Splice_Rec_1958138,Human_Splice_Rec_1958139,Human_Splice_Rec_1958192,Human_Splice_Rec_1958193,Human_Splice_Rec_1958246,Human_Splice_Rec_1958247,Human_Splice_Rec_1958296,Human_Splice_Rec_1958297,Human_Splice_Rec_1958346,Human_Splice_Rec_1958347,Human_Splice_Rec_1958398,Human_Splice_Rec_1958399,Human_Splice_Rec_1958448,Human_Splice_Rec_1958449,Human_Splice_Rec_1958502,Human_Splice_Rec_1958503,Human_Splice_Rec_1958530,Human_Splice_Rec_1958531,Human_Splice_Rec_1958578,Human_Splice_Rec_1958579,Human_Splice_Rec_1958618,Human_Splice_Rec_1958619,Human_Splice_Rec_1958664,Human_Splice_Rec_1958665,Human_Splice_Rec_1958714,Human_Splice_Rec_1958715,Human_Splice_Rec_1958764,Human_Splice_Rec_1958765,Human_Splice_Rec_1958808,Human_Splice_Rec_1958809,Human_Splice_Rec_1958828,Human_Splice_Rec_1958829 Clinvar_Rec_395 RMVar_hsa_circ_2241,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_51785,RMVar_hsa_circ_80212,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192481,RMVar_hsa_circ_20169,RMVar_hsa_circ_283257,RMVar_hsa_circ_192482,RMVar_hsa_circ_21252,RMVar_hsa_circ_114765,RMVar_hsa_circ_192483,RMVar_hsa_circ_192484 81749 RMVar_ID_81749 Human_SNP_ID_658369398 m1A Human chr19 - 11012928 11012928 11012928 CAAACCTTTGATCTGCAAGGACAGATGCGGCCACGCCAGGACTGAAGGCCGGGTCGGACACCAGA CAAACCTTTGATCTGCAAGGACAGATGCGGCCCCGCCAGGACTGAAGGCCGGGTCGGACACCAGA T G AC011442.1 Ensembl:ENSG00000266936 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11012926..11013100 32194978 MeRIP-seq:(Medium) rs931896064 Functional Loss SNV dbSNP153 33..33 33 - - - 81750 RMVar_ID_81750 Human_SNP_ID_658375589 m1A Human chr19 - 11034202 11034202 11034202 GCCTGAACTGCCCCATCCAGCCTGCAGCGCTTACCATGAACAGATCAAACTCCTCCTCGTGCCGG GCCTGAACTGCCCCATCCAGCCTGCAGCGCTTGCCATGAACAGATCAAACTCCTCCTCGTGCCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:11034151..11034225;chr19:11034176..11034225 26863196 MeRIP-seq:(Medium) rs1555785056 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_396 81751 RMVar_ID_81751 Human_SNP_ID_658375853 m1A Human chr19 + 11034974 11034974 11034974 AGGCCCGCAACCCCAAGCGGAAGCCGCGCCTCATGGAGGAGGACGAGCTCCCCTCGTGGATCATC AGGCCCGCAACCCCAAGCGGAAGCCGCGCCTCGTGGAGGAGGACGAGCTCCCCTCGTGGATCATC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11034901..11034975 26863196 MeRIP-seq:(Medium) rs1555785383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500194,Human_RBP_ID_8839123,Human_RBP_ID_9293416 Human_Splice_Rec_1956920,Human_Splice_Rec_1956986,Human_Splice_Rec_1957054,Human_Splice_Rec_1957122,Human_Splice_Rec_1957190,Human_Splice_Rec_1957256,Human_Splice_Rec_1957320,Human_Splice_Rec_1957388,Human_Splice_Rec_1957452,Human_Splice_Rec_1957520,Human_Splice_Rec_1957590,Human_Splice_Rec_1957664,Human_Splice_Rec_1957732,Human_Splice_Rec_1957798,Human_Splice_Rec_1957864,Human_Splice_Rec_1957930,Human_Splice_Rec_1957996,Human_Splice_Rec_1958060,Human_Splice_Rec_1958170,Human_Splice_Rec_1958222,Human_Splice_Rec_1958276,Human_Splice_Rec_1958328,Human_Splice_Rec_1958378,Human_Splice_Rec_1958430,Human_Splice_Rec_1958480,Human_Splice_Rec_1958560,Human_Splice_Rec_1958610,Human_Splice_Rec_1958650,Human_Splice_Rec_1958694,Human_Splice_Rec_1958746,Human_Splice_Rec_1958796,Human_Splice_Rec_1958858,Human_Splice_Rec_1958898,Human_Splice_Rec_1958934,Human_Splice_Rec_1958978,Human_Splice_Rec_1959012,Human_Splice_Rec_1959032,Human_Splice_Rec_1959062,Human_Splice_Rec_1959084,Human_Splice_Rec_1959104,Human_Splice_Rec_1959114 Clinvar_Rec_397 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_283144,RMVar_hsa_circ_14259,RMVar_hsa_circ_74005,RMVar_hsa_circ_325575,RMVar_hsa_circ_367421,RMVar_hsa_circ_82983,RMVar_hsa_circ_192492,RMVar_hsa_circ_192491 81752 RMVar_ID_81752 Human_SNP_ID_658377635 m1A Human chr19 + 11041363 11041363 11041363 GAGATCGAAGAGGAGGTCCGGCAGAAGAAATCATCACGGAAGCGCAAGCGAGACAGCGACGCCGG GAGATCGAAGAGGAGGTCCGGCAGAAGAAATCGTCACGGAAGCGCAAGCGAGACAGCGACGCCGG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:11041259..11041575;chr19:11041244..11041597 26863196 MeRIP-seq:(Medium) rs61761958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53741,Human_RBP_ID_8255772,Human_RBP_ID_17694515,Human_RBP_ID_24545713,Human_RBP_ID_26815278,Human_RBP_ID_26982169 Human_Splice_Rec_1956922,Human_Splice_Rec_1957058,Human_Splice_Rec_1957126,Human_Splice_Rec_1957192,Human_Splice_Rec_1957324,Human_Splice_Rec_1957454,Human_Splice_Rec_1957522,Human_Splice_Rec_1957592,Human_Splice_Rec_1957666,Human_Splice_Rec_1957866,Human_Splice_Rec_1957932,Human_Splice_Rec_1958064,Human_Splice_Rec_1958224,Human_Splice_Rec_1958380,Human_Splice_Rec_1958482,Human_Splice_Rec_1958562,Human_Splice_Rec_1958698,Human_Splice_Rec_1958748,Human_Splice_Rec_1958798,Human_Splice_Rec_1958860,Human_Splice_Rec_1958900,Human_Splice_Rec_1958980,Human_Splice_Rec_1959066,Human_Splice_Rec_1959086,Human_Splice_Rec_1959116,Human_Splice_Rec_1959128 Clinvar_Rec_398,Clinvar_Rec_399,Clinvar_Rec_400 RMVar_hsa_circ_51477,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_8398,RMVar_hsa_circ_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491,RMVar_hsa_circ_342715,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_321984,RMVar_hsa_circ_11136 81753 RMVar_ID_81753 Human_SNP_ID_658377636 m1A Human chr19 + 11041363 11041363 11041363 GAGATCGAAGAGGAGGTCCGGCAGAAGAAATCATCACGGAAGCGCAAGCGAGACAGCGACGCCGG GAGATCGAAGAGGAGGTCCGGCAGAAGAAATCTTCACGGAAGCGCAAGCGAGACAGCGACGCCGG A T SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:11041259..11041575;chr19:11041244..11041597 26863196 MeRIP-seq:(Medium) rs61761958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53741,Human_RBP_ID_8255772,Human_RBP_ID_17694515,Human_RBP_ID_24545713,Human_RBP_ID_26815278,Human_RBP_ID_26982169 Human_Splice_Rec_1956922,Human_Splice_Rec_1957058,Human_Splice_Rec_1957126,Human_Splice_Rec_1957192,Human_Splice_Rec_1957324,Human_Splice_Rec_1957454,Human_Splice_Rec_1957522,Human_Splice_Rec_1957592,Human_Splice_Rec_1957666,Human_Splice_Rec_1957866,Human_Splice_Rec_1957932,Human_Splice_Rec_1958064,Human_Splice_Rec_1958224,Human_Splice_Rec_1958380,Human_Splice_Rec_1958482,Human_Splice_Rec_1958562,Human_Splice_Rec_1958698,Human_Splice_Rec_1958748,Human_Splice_Rec_1958798,Human_Splice_Rec_1958860,Human_Splice_Rec_1958900,Human_Splice_Rec_1958980,Human_Splice_Rec_1959066,Human_Splice_Rec_1959086,Human_Splice_Rec_1959116,Human_Splice_Rec_1959128 Clinvar_Rec_398,Clinvar_Rec_399,Clinvar_Rec_400 RMVar_hsa_circ_51477,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_8398,RMVar_hsa_circ_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491,RMVar_hsa_circ_342715,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_321984,RMVar_hsa_circ_11136 81754 RMVar_ID_81754 Human_SNP_ID_658382657 m1A Human chr19 + 11058326 11058326 11058326 GCCCTCGCGAAAGGAGCTGCCCGAGTACTACGAGCTCATCCGCAAGCCCGTGGACTTCAAGAAGA GCCCTCGCGAAAGGAGCTGCCCGAGTACTACGCGCTCATCCGCAAGCCCGTGGACTTCAAGAAGA A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11033499..11058853 32194978 MeRIP-seq:(Medium) rs1555795056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53745,Human_RBP_ID_9382030 Human_Splice_Rec_1956924,Human_Splice_Rec_1956925,Human_Splice_Rec_1956990,Human_Splice_Rec_1956991,Human_Splice_Rec_1957060,Human_Splice_Rec_1957061,Human_Splice_Rec_1957128,Human_Splice_Rec_1957129,Human_Splice_Rec_1957194,Human_Splice_Rec_1957195,Human_Splice_Rec_1957258,Human_Splice_Rec_1957259,Human_Splice_Rec_1957326,Human_Splice_Rec_1957327,Human_Splice_Rec_1957390,Human_Splice_Rec_1957391,Human_Splice_Rec_1957456,Human_Splice_Rec_1957457,Human_Splice_Rec_1957524,Human_Splice_Rec_1957525,Human_Splice_Rec_1957594,Human_Splice_Rec_1957595,Human_Splice_Rec_1957668,Human_Splice_Rec_1957669,Human_Splice_Rec_1957734,Human_Splice_Rec_1957735,Human_Splice_Rec_1957800,Human_Splice_Rec_1957801,Human_Splice_Rec_1957868,Human_Splice_Rec_1957869,Human_Splice_Rec_1957934,Human_Splice_Rec_1957935,Human_Splice_Rec_1957998,Human_Splice_Rec_1957999,Human_Splice_Rec_1958066,Human_Splice_Rec_1958067,Human_Splice_Rec_1958172,Human_Splice_Rec_1958173,Human_Splice_Rec_1958228,Human_Splice_Rec_1958229,Human_Splice_Rec_1958278,Human_Splice_Rec_1958279,Human_Splice_Rec_1958330,Human_Splice_Rec_1958331,Human_Splice_Rec_1958382,Human_Splice_Rec_1958383,Human_Splice_Rec_1958432,Human_Splice_Rec_1958433,Human_Splice_Rec_1958486,Human_Splice_Rec_1958487,Human_Splice_Rec_1958564,Human_Splice_Rec_1958565,Human_Splice_Rec_1958652,Human_Splice_Rec_1958653,Human_Splice_Rec_1958700,Human_Splice_Rec_1958701,Human_Splice_Rec_1958750,Human_Splice_Rec_1958751,Human_Splice_Rec_1958800,Human_Splice_Rec_1958801,Human_Splice_Rec_1958862,Human_Splice_Rec_1958863,Human_Splice_Rec_1958902,Human_Splice_Rec_1958903,Human_Splice_Rec_1958936,Human_Splice_Rec_1958937,Human_Splice_Rec_1958982,Human_Splice_Rec_1958983,Human_Splice_Rec_1959034,Human_Splice_Rec_1959035,Human_Splice_Rec_1959068,Human_Splice_Rec_1959069,Human_Splice_Rec_1959088,Human_Splice_Rec_1959089,Human_Splice_Rec_1959106,Human_Splice_Rec_1959107,Human_Splice_Rec_1959118,Human_Splice_Rec_1959119,Human_Splice_Rec_1959130,Human_Splice_Rec_1959131,Human_Splice_Rec_1959134,Human_Splice_Rec_1959135,Human_Splice_Rec_1959144,Human_Splice_Rec_1959145,Human_Splice_Rec_1959156,Human_Splice_Rec_1959157 Human_miRNA_ID_2894795,Human_miRNA_ID_2894796,Human_miRNA_ID_2894797 Clinvar_Rec_401 RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_192489,RMVar_hsa_circ_8398,RMVar_hsa_circ_192495,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_11136,RMVar_hsa_circ_192494,RMVar_hsa_circ_277811,RMVar_hsa_circ_308346 81755 RMVar_ID_81755 Human_SNP_ID_658383211 m1A Human chr19 - 11059917 11059916 11059917 CTGGGGCCTTGGGGGCTCTCGGGCCAGCGTGAACCCCGGCGTCCTGAACCCCCCCGGGACTCACA CTGGGGCCTTGGGGGCTCTCGGGCCAGCGTGA_CCCCGGCGTCCTGAACCCCCCCGGGACTCACA GT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:11059911..11060031 26863196 MeRIP-seq:(Medium) rs776651662 Functional Loss DEL dbSNP153 33..33 33 - - - 81756 RMVar_ID_81756 Human_SNP_ID_658383313 m1A Human chr19 - 11060102 11060102 11060102 ACCCTCGGCTCGGCCGCCGCCGGCCGCCCTTCAGCCGGTCCTGTGCCTTCTCCTTCCGGCCAAGC ACCCTCGGCTCGGCCGCCGCCGGCCGCCCTTCGGCCGGTCCTGTGCCTTCTCCTTCCGGCCAAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11059715..11061996 26863196 MeRIP-seq:(Medium) rs755493468 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_402 81757 RMVar_ID_81757 Human_SNP_ID_658383315 m1A Human chr19 + 11060105 11060105 11060105 TGGCCGGAAGGAGAAGGCACAGGACCGGCTGAAGGGCGGCCGGCGGCGGCCGAGCCGAGGGTCCC TGGCCGGAAGGAGAAGGCACAGGACCGGCTGACGGGCGGCCGGCGGCGGCCGAGCCGAGGGTCCC A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:11060059..11060213 26863196 MeRIP-seq:(Medium) rs1555796263 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_53747,Human_RBP_ID_8839792,Human_RBP_ID_17935243,Human_RBP_ID_18412498,Human_RBP_ID_24545440,Human_RBP_ID_26335720,Human_RBP_ID_27815140 Human_Splice_Rec_1956930,Human_Splice_Rec_1956931,Human_Splice_Rec_1956996,Human_Splice_Rec_1956997,Human_Splice_Rec_1957066,Human_Splice_Rec_1957067,Human_Splice_Rec_1957134,Human_Splice_Rec_1957135,Human_Splice_Rec_1957200,Human_Splice_Rec_1957201,Human_Splice_Rec_1957264,Human_Splice_Rec_1957265,Human_Splice_Rec_1957332,Human_Splice_Rec_1957333,Human_Splice_Rec_1957396,Human_Splice_Rec_1957397,Human_Splice_Rec_1957462,Human_Splice_Rec_1957463,Human_Splice_Rec_1957530,Human_Splice_Rec_1957531,Human_Splice_Rec_1957600,Human_Splice_Rec_1957601,Human_Splice_Rec_1957674,Human_Splice_Rec_1957675,Human_Splice_Rec_1957740,Human_Splice_Rec_1957741,Human_Splice_Rec_1957806,Human_Splice_Rec_1957807,Human_Splice_Rec_1957874,Human_Splice_Rec_1957875,Human_Splice_Rec_1957940,Human_Splice_Rec_1957941,Human_Splice_Rec_1958004,Human_Splice_Rec_1958005,Human_Splice_Rec_1958072,Human_Splice_Rec_1958073,Human_Splice_Rec_1958178,Human_Splice_Rec_1958179,Human_Splice_Rec_1958234,Human_Splice_Rec_1958235,Human_Splice_Rec_1958284,Human_Splice_Rec_1958285,Human_Splice_Rec_1958336,Human_Splice_Rec_1958337,Human_Splice_Rec_1958388,Human_Splice_Rec_1958389,Human_Splice_Rec_1958438,Human_Splice_Rec_1958439,Human_Splice_Rec_1958492,Human_Splice_Rec_1958493,Human_Splice_Rec_1958570,Human_Splice_Rec_1958571,Human_Splice_Rec_1958656,Human_Splice_Rec_1958657,Human_Splice_Rec_1958706,Human_Splice_Rec_1958707,Human_Splice_Rec_1958756,Human_Splice_Rec_1958757,Human_Splice_Rec_1958804,Human_Splice_Rec_1958805,Human_Splice_Rec_1958868,Human_Splice_Rec_1958869,Human_Splice_Rec_1958908,Human_Splice_Rec_1958909,Human_Splice_Rec_1958942,Human_Splice_Rec_1958943,Human_Splice_Rec_1958988,Human_Splice_Rec_1958989,Human_Splice_Rec_1959040,Human_Splice_Rec_1959041,Human_Splice_Rec_1959074,Human_Splice_Rec_1959075,Human_Splice_Rec_1959094,Human_Splice_Rec_1959095,Human_Splice_Rec_1959110,Human_Splice_Rec_1959111,Human_Splice_Rec_1959124,Human_Splice_Rec_1959125,Human_Splice_Rec_1959140,Human_Splice_Rec_1959141,Human_Splice_Rec_1959150,Human_Splice_Rec_1959151 Human_miRNA_ID_1967938,Human_miRNA_ID_1967939,Human_miRNA_ID_1967940 Clinvar_Rec_403 RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_192489,RMVar_hsa_circ_8398,RMVar_hsa_circ_192495,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_192494,RMVar_hsa_circ_277811,RMVar_hsa_circ_308346,RMVar_hsa_circ_192496,RMVar_hsa_circ_301128 81758 RMVar_ID_81758 Human_SNP_ID_658383971 m1A Human chr19 - 11061732 11061720 11061733 AGAGAGTGTGCGTTGGCCACCCCTGCCAGGGCACCTTGCCAGGGACCTGCCAAACTTTAAATAAA AGAGAGTGTGCGTTGGCCACCCCTGCCAGGG_____________ACCTGCCAAACTTTAAATAAA TCCCTGGCAAGGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11061731..11061900 26863196 MeRIP-seq:(Medium) rs1004320359 Functional Loss DEL dbSNP153 32..44 33 - - - 81759 RMVar_ID_81759 Human_SNP_ID_658391812 m1A Human chr19 + 11089524 11089524 11089524 CTAGGACACAGCAGGTCGTGATCCGGGTCGGGACACTGCCTGGCAGAGGCTGCGAGCATGGGGCC CTAGGACACAGCAGGTCGTGATCCGGGTCGGGTCACTGCCTGGCAGAGGCTGCGAGCATGGGGCC A T LDLR Ensembl:ENSG00000130164 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11089451..11089770 26863196 MeRIP-seq:(Medium) rs750462653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55293,Human_RBP_ID_512737,Human_RBP_ID_773857,Human_RBP_ID_4557223,Human_RBP_ID_5585304,Human_RBP_ID_6718425,Human_RBP_ID_8839793,Human_RBP_ID_13364783,Human_RBP_ID_22447383,Human_RBP_ID_22977405 Human_Splice_Rec_1959161,Human_Splice_Rec_1959195,Human_Splice_Rec_1959197,Human_Splice_Rec_1959201,Human_Splice_Rec_1959231,Human_Splice_Rec_1959263,Human_Splice_Rec_1959293,Human_Splice_Rec_1959327 81760 RMVar_ID_81760 Human_SNP_ID_658391813 m1A Human chr19 + 11089526 11089526 11089526 AGGACACAGCAGGTCGTGATCCGGGTCGGGACACTGCCTGGCAGAGGCTGCGAGCATGGGGCCCT AGGACACAGCAGGTCGTGATCCGGGTCGGGACCCTGCCTGGCAGAGGCTGCGAGCATGGGGCCCT A C LDLR Ensembl:ENSG00000130164 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11089476..11089651 26863196 MeRIP-seq:(Medium) rs763282380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55293,Human_RBP_ID_512737,Human_RBP_ID_773857,Human_RBP_ID_4557223,Human_RBP_ID_8839793,Human_RBP_ID_13364783,Human_RBP_ID_22447383,Human_RBP_ID_22977405 Human_Splice_Rec_1959161,Human_Splice_Rec_1959195,Human_Splice_Rec_1959197,Human_Splice_Rec_1959201,Human_Splice_Rec_1959231,Human_Splice_Rec_1959263,Human_Splice_Rec_1959293,Human_Splice_Rec_1959327 Clinvar_Rec_404 81761 RMVar_ID_81761 Human_SNP_ID_658391853 m1A Human chr19 - 11089588 11089587 11089588 CTTACCTGCAGTCCCCGCCGCGGCGAGGAGCAAGGCGACGGTCCAGCGCAATTTCCAGCCCCAGG CTTACCTGCAGTCCCCGCCGCGGCGAGGAGCA_GGCGACGGTCCAGCGCAATTTCCAGCCCCAGG CT C LDLR-AS1-001 RNACentral:URS0000EEACD7 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:11089539..11089700 26863196 MeRIP-seq:(Medium) rs879254388 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_405,Clinvar_Rec_406 81762 RMVar_ID_81762 Human_SNP_ID_658396334 m1A Human chr19 + 11105325 11105325 11105325 CTCAGACCGGGACTGCTTGGACGGCTCAGACGAGGCCTCCTGCCCGGTGCTCACCTGTGGTCCCG CTCAGACCGGGACTGCTTGGACGGCTCAGACGGGGCCTCCTGCCCGGTGCTCACCTGTGGTCCCG A G LDLR Ensembl:ENSG00000130164 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11105275..11105398 26863196 MeRIP-seq:(Medium) rs879254519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138015,Human_RBP_ID_8839798,Human_RBP_ID_22447387,Human_RBP_ID_22719090,Human_RBP_ID_22763222,Human_RBP_ID_22977409 Clinvar_Rec_407 RMVar_hsa_circ_5611,RMVar_hsa_circ_322490,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,RMVar_hsa_circ_34618,RMVar_hsa_circ_192500,RMVar_hsa_circ_378050,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308,RMVar_hsa_circ_304355,RMVar_hsa_circ_318266,RMVar_hsa_circ_331393,RMVar_hsa_circ_308678,RMVar_hsa_circ_13639,RMVar_hsa_circ_192501 81763 RMVar_ID_81763 Human_SNP_ID_658396335 m1A Human chr19 - 11105333 11105326 11105333 GAAGCTGGCGGGACCACAGGTGAGCACCGGGCAGGAGGCCTCGTCTGAGCCGTCCAAGCAGTCCC GAAGCTGGCGGGACCACAGGTGAGCACCGGGC_______CTCGTCTGAGCCGTCCAAGCAGTCCC GGCCTCCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11105282..11105373 26863196 MeRIP-seq:(Medium) rs879254521 Functional Loss DEL dbSNP153 33..39 33 - - - Clinvar_Rec_408 81764 RMVar_ID_81764 Human_SNP_ID_658396341 m1A Human chr19 - 11105333 11105333 11105333 GAAGCTGGCGGGACCACAGGTGAGCACCGGGCAGGAGGCCTCGTCTGAGCCGTCCAAGCAGTCCC GAAGCTGGCGGGACCACAGGTGAGCACCGGGCGGGAGGCCTCGTCTGAGCCGTCCAAGCAGTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11105282..11105373 26863196 MeRIP-seq:(Medium) rs875989901 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_409,Clinvar_Rec_410 GWAS_ID_9618 81765 RMVar_ID_81765 Human_SNP_ID_658396342 m1A Human chr19 - 11105333 11105333 11105333 GAAGCTGGCGGGACCACAGGTGAGCACCGGGCAGGAGGCCTCGTCTGAGCCGTCCAAGCAGTCCC GAAGCTGGCGGGACCACAGGTGAGCACCGGGCCGGAGGCCTCGTCTGAGCCGTCCAAGCAGTCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11105282..11105373 26863196 MeRIP-seq:(Medium) rs875989901 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_409,Clinvar_Rec_410 GWAS_ID_9618 81766 RMVar_ID_81766 Human_SNP_ID_658396361 m1A Human chr19 - 11105350 11105350 11105350 GTGGAGCTGTTGCACTGGAAGCTGGCGGGACCACAGGTGAGCACCGGGCAGGAGGCCTCGTCTGA GTGGAGCTGTTGCACTGGAAGCTGGCGGGACCCCAGGTGAGCACCGGGCAGGAGGCCTCGTCTGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11105301..11105400 32194978 MeRIP-seq:(Medium) rs879254528 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_411 81767 RMVar_ID_81767 Human_SNP_ID_658397375 m1A Human chr19 + 11107494 11107494 11107494 CAACATGGCTAGAGACTGCCGGGACTGGTCAGATGAACCCATCAAAGAGTGCGGTGAGTCTCGGT CAACATGGCTAGAGACTGCCGGGACTGGTCAGGTGAACCCATCAAAGAGTGCGGTGAGTCTCGGT A G LDLR Ensembl:ENSG00000130164 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11107444..11107563 26863196 MeRIP-seq:(Medium) rs1555803908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2555860,Human_RBP_ID_22763228,Human_RBP_ID_26335726 Human_Splice_Rec_1959171,Human_Splice_Rec_1959207,Human_Splice_Rec_1959239,Human_Splice_Rec_1959271,Human_Splice_Rec_1959303,Human_Splice_Rec_1959337,Human_Splice_Rec_1959371,Human_Splice_Rec_1959399 Clinvar_Rec_412 RMVar_hsa_circ_5611,RMVar_hsa_circ_322490,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_1058,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,RMVar_hsa_circ_192500,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308,RMVar_hsa_circ_304355,RMVar_hsa_circ_318266,RMVar_hsa_circ_308678,RMVar_hsa_circ_13639,RMVar_hsa_circ_192502,RMVar_hsa_circ_78608,RMVar_hsa_circ_78993,RMVar_hsa_circ_192503,RMVar_hsa_circ_45258,RMVar_hsa_circ_278995,RMVar_hsa_circ_310372,RMVar_hsa_circ_341764,RMVar_hsa_circ_303678,RMVar_hsa_circ_274108,RMVar_hsa_circ_192504,RMVar_hsa_circ_192505,RMVar_hsa_circ_80946,RMVar_hsa_circ_375833,RMVar_hsa_circ_192506,RMVar_hsa_circ_192507 81768 RMVar_ID_81768 Human_SNP_ID_658397751 m1A Human chr19 + 11108612 11108612 11108612 CTCGTCCTGGTGAGGGTTTTTTTTTTTCCCCAACCCTCTGTGGTGGATACTGAAAGACCATATTA CTCGTCCTGGTGAGGGTTTTTTTTTTTCCCCAGCCCTCTGTGGTGGATACTGAAAGACCATATTA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:11108593..11108677 26863410 MeRIP-seq:(Medium) rs1189808612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568432 RMVar_hsa_circ_5611,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_1058,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,RMVar_hsa_circ_192500,RMVar_hsa_circ_19308,RMVar_hsa_circ_304355,RMVar_hsa_circ_318266,RMVar_hsa_circ_13639,RMVar_hsa_circ_192502,RMVar_hsa_circ_78608,RMVar_hsa_circ_78993,RMVar_hsa_circ_192503,RMVar_hsa_circ_45258,RMVar_hsa_circ_310372,RMVar_hsa_circ_341764,RMVar_hsa_circ_303678,RMVar_hsa_circ_274108,RMVar_hsa_circ_192505,RMVar_hsa_circ_80946,RMVar_hsa_circ_192506 81769 RMVar_ID_81769 Human_SNP_ID_658398284 m1A Human chr19 - 11110701 11110652 11110701 GGGCACAGGCACTCGTAGCCGATCTTAAGGTCATTGCAGACGTGGGAACAGCCGCCGTTGTTGTC GGGCACAGGCACTCGTAGCCGATCTTAAGGTC_________________________________ GGACCAACGAATGCTTGGACAACAACGGCGGCTGTTCCCACGTCTGCAAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11110609..11110775 26863196 MeRIP-seq:(Medium) rs879254736 Functional Loss DEL dbSNP153 33..65 33 - - - Clinvar_Rec_413 81770 RMVar_ID_81770 Human_SNP_ID_658398336 m1A Human chr19 - 11110701 11110701 11110701 GGGCACAGGCACTCGTAGCCGATCTTAAGGTCATTGCAGACGTGGGAACAGCCGCCGTTGTTGTC GGGCACAGGCACTCGTAGCCGATCTTAAGGTCTTTGCAGACGTGGGAACAGCCGCCGTTGTTGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11110609..11110775 26863196 MeRIP-seq:(Medium) rs1568600400 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_414 81771 RMVar_ID_81771 Human_SNP_ID_658400788 m1A Human chr19 + 11116925 11116920 11116926 CAAACTTCACTCCATCTCAAGCATCGATGTCAACGGGGGCAACCGGAAGACCATCTTGGAGGATG CAAACTTCACTCCATCTCAAGCATCGAT______GGGGGCAACCGGAAGACCATCTTGGAGGATG TGTCAAC T LDLR Ensembl:ENSG00000130164 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:11116901..11116925 32194978 MeRIP-seq:(Medium) rs1555806467 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_53839,Human_RBP_ID_912519,Human_RBP_ID_9380538,Human_RBP_ID_22763244,Human_RBP_ID_27816100 Human_Splice_Rec_1959182,Human_Splice_Rec_1959183,Human_Splice_Rec_1959218,Human_Splice_Rec_1959219,Human_Splice_Rec_1959250,Human_Splice_Rec_1959251,Human_Splice_Rec_1959282,Human_Splice_Rec_1959283,Human_Splice_Rec_1959314,Human_Splice_Rec_1959315,Human_Splice_Rec_1959348,Human_Splice_Rec_1959349,Human_Splice_Rec_1959382,Human_Splice_Rec_1959383 Human_miRNA_ID_1535944,Human_miRNA_ID_2669012,Human_miRNA_ID_2669013,Human_miRNA_ID_2722706,Human_miRNA_ID_2722707 Clinvar_Rec_415 RMVar_hsa_circ_344045,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_19308,RMVar_hsa_circ_13639,RMVar_hsa_circ_78608,RMVar_hsa_circ_192503,RMVar_hsa_circ_45258,RMVar_hsa_circ_274108,RMVar_hsa_circ_51705,RMVar_hsa_circ_62160,RMVar_hsa_circ_192519,RMVar_hsa_circ_50951,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515,RMVar_hsa_circ_284631,RMVar_hsa_circ_347763,RMVar_hsa_circ_373868,RMVar_hsa_circ_299827,RMVar_hsa_circ_99690,RMVar_hsa_circ_76246,RMVar_hsa_circ_192517,RMVar_hsa_circ_192518,RMVar_hsa_circ_192516,RMVar_hsa_circ_376040,RMVar_hsa_circ_192520 81772 RMVar_ID_81772 Human_SNP_ID_658400790 m1A Human chr19 + 11116925 11116925 11116925 CAAACTTCACTCCATCTCAAGCATCGATGTCAACGGGGGCAACCGGAAGACCATCTTGGAGGATG CAAACTTCACTCCATCTCAAGCATCGATGTCAGCGGGGGCAACCGGAAGACCATCTTGGAGGATG A G LDLR Ensembl:ENSG00000130164 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:11116901..11116925 32194978 MeRIP-seq:(Medium) rs770297500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53839,Human_RBP_ID_912519,Human_RBP_ID_9380538,Human_RBP_ID_22763244,Human_RBP_ID_27816100 Human_Splice_Rec_1959182,Human_Splice_Rec_1959183,Human_Splice_Rec_1959218,Human_Splice_Rec_1959219,Human_Splice_Rec_1959250,Human_Splice_Rec_1959251,Human_Splice_Rec_1959282,Human_Splice_Rec_1959283,Human_Splice_Rec_1959314,Human_Splice_Rec_1959315,Human_Splice_Rec_1959348,Human_Splice_Rec_1959349,Human_Splice_Rec_1959382,Human_Splice_Rec_1959383 Human_miRNA_ID_1535944,Human_miRNA_ID_2669012,Human_miRNA_ID_2669013,Human_miRNA_ID_2722706,Human_miRNA_ID_2722707 RMVar_hsa_circ_344045,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_19308,RMVar_hsa_circ_13639,RMVar_hsa_circ_78608,RMVar_hsa_circ_192503,RMVar_hsa_circ_45258,RMVar_hsa_circ_274108,RMVar_hsa_circ_51705,RMVar_hsa_circ_62160,RMVar_hsa_circ_192519,RMVar_hsa_circ_50951,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515,RMVar_hsa_circ_284631,RMVar_hsa_circ_347763,RMVar_hsa_circ_373868,RMVar_hsa_circ_299827,RMVar_hsa_circ_99690,RMVar_hsa_circ_76246,RMVar_hsa_circ_192517,RMVar_hsa_circ_192518,RMVar_hsa_circ_192516,RMVar_hsa_circ_376040,RMVar_hsa_circ_192520 81773 RMVar_ID_81773 Human_SNP_ID_658402089 m1A Human chr19 - 11120427 11120424 11120428 TGGGCGAGTGGGGGTTGATCTGCGGGGCAGGGAGGCACAGATACTGGCAGCCGCCATTGCTCAGG TGGGCGAGTGGGGGTTGATCTGCGGGGCAGG____CACAGATACTGGCAGCCGCCATTGCTCAGG GCCTC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11120264..11120450 26863196 MeRIP-seq:(Medium) rs879255120 Functional Loss DEL dbSNP153 32..35 33 - - - Clinvar_Rec_416 81774 RMVar_ID_81774 Human_SNP_ID_658402095 m1A Human chr19 - 11120427 11120427 11120427 TGGGCGAGTGGGGGTTGATCTGCGGGGCAGGGAGGCACAGATACTGGCAGCCGCCATTGCTCAGG TGGGCGAGTGGGGGTTGATCTGCGGGGCAGGGGGGCACAGATACTGGCAGCCGCCATTGCTCAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11120264..11120450 26863196 MeRIP-seq:(Medium) rs879255119 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_417 81775 RMVar_ID_81775 Human_SNP_ID_658402146 m1A Human chr19 - 11120468 11120468 11120468 CCTGGCCAGCAGCATGCCGTCCGGGCAGGCGCAGGTAAACTTGGGCGAGTGGGGGTTGATCTGCG CCTGGCCAGCAGCATGCCGTCCGGGCAGGCGCGGGTAAACTTGGGCGAGTGGGGGTTGATCTGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11120351..11120525 26863196 MeRIP-seq:(Medium) rs1555807435 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_418 81776 RMVar_ID_81776 Human_SNP_ID_658405723 m1A Human chr19 - 11131659 11131657 11131660 TTGGTGCCATCTGCTGTTGTGTGTTGAAAGCCACTTGCTTCTCTGGGCCTGACATCCCCTCCCCT TTGGTGCCATCTGCTGTTGTGTGTTGAAAGC___TTGCTTCTCTGGGCCTGACATCCCCTCCCCT AGTG A SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11131609..11131714 26863196 MeRIP-seq:(Medium) rs1206263668 Functional Loss DEL dbSNP153 32..34 33 - - - 81777 RMVar_ID_81777 Human_SNP_ID_658405735 m1A Human chr19 - 11131708 11131696 11131708 AGGGGTTTGGCTTAGAGATTGGTGGATGAGGCAGGGCCAGGGGGTCCCGTTGGTGCCATCTGCTG AGGGGTTTGGCTTAGAGATTGGTGGATGAGGC____________TCCCGTTGGTGCCATCTGCTG ACCCCCTGGCCCT A SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11131657..11131780 26863196 MeRIP-seq:(Medium) rs1479533551 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_6718468,Human_RBP_ID_13365079 81778 RMVar_ID_81778 Human_SNP_ID_658410446 m1A Human chr19 - 11146826 11146826 11146826 TCCACCCGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTCCAGGCGTGAGCCATCGTGCCCAGCTA TCCACCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCATCGTGCCCAGCTA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs150519327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365487,Human_RBP_ID_23173790 81779 RMVar_ID_81779 Human_SNP_ID_658410503 m1A Human chr19 - 11147041 11147041 11147041 AGTTTCACTCTTGTTGTCCAGTCTGGAGTGCAATGGCACAATCTCAGCTCACAGCAACCTCTGCC AGTTTCACTCTTGTTGTCCAGTCTGGAGTGCAGTGGCACAATCTCAGCTCACAGCAACCTCTGCC T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1443128487 Functional Loss SNV dbSNP153 33..33 33 - - - 81780 RMVar_ID_81780 Human_SNP_ID_658411239 m1A Human chr19 + 11149226 11149226 11149226 CATTGAGAAGGCTCTGGGCCACTTCCTTCTCCATGGTGAGGATCTCTGCAGGGTGGAGAGAAGCA CATTGAGAAGGCTCTGGGCCACTTCCTTCTCCCTGGTGAGGATCTCTGCAGGGTGGAGAGAAGCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11149076..11149250 32194978 MeRIP-seq:(Medium) rs1423817741 Functional Loss SNV dbSNP153 33..33 33 - - - 81781 RMVar_ID_81781 Human_SNP_ID_658413116 m1A Human chr19 - 11155697 11155697 11155697 CCTGCTGGGCGCCAACCGCGCGGAGGCGCAGCAGCGACGGCTGCTGGGGCGCCACGAGCAGGTGG CCTGCTGGGCGCCAACCGCGCGGAGGCGCAGCGGCGACGGCTGCTGGGGCGCCACGAGCAGGTGG T C SPC24 Ensembl:ENSG00000161888 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11155549..11155750 32194978 MeRIP-seq:(Medium) rs1443862863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558088,Human_RBP_ID_18420852,Human_RBP_ID_22977659 Human_Splice_Rec_1959419,Human_Splice_Rec_1959427,Human_Splice_Rec_1959433,Human_Splice_Rec_1959439,Human_Splice_Rec_1959445,Human_Splice_Rec_1959451,Human_Splice_Rec_1959455 RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 81782 RMVar_ID_81782 Human_SNP_ID_658413146 m1A Human chr19 - 11155742 11155742 11155742 GGCCGCCTTCCGCGACATAGAGGAGGTGAGCCAGGGGCTGCTCAGCCTGCTGGGCGCCAACCGCG GGCCGCCTTCCGCGACATAGAGGAGGTGAGCCGGGGGCTGCTCAGCCTGCTGGGCGCCAACCGCG T C SPC24 Ensembl:ENSG00000161888 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:11155564..11155800;chr19:11147974..11155800;chr19:11155537..11155800;chr19:11148068..11155800 26863196 MeRIP-seq:(Medium) rs1048454297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500488,Human_RBP_ID_6718617,Human_RBP_ID_18420852,Human_RBP_ID_18722040,Human_RBP_ID_22446435 RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 81783 RMVar_ID_81783 Human_SNP_ID_658424501 m1A Human chr19 - 11193367 11193367 11193367 AGTACAACTTAAGAGCCAGAAGTTCCTGGGCCACCCCACAGCGGGCCGGGGTCGCAGCGAGCTCT AGTACAACTTAAGAGCCAGAAGTTCCTGGGCCTCCCCACAGCGGGCCGGGGTCGCAGCGAGCTCT T A KANK2 Ensembl:ENSG00000197256 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11193320..11193455 26863196 MeRIP-seq:(Medium) rs1470041532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1959540 RMVar_hsa_circ_69603,RMVar_hsa_circ_361073 81784 RMVar_ID_81784 Human_SNP_ID_658425403 m1A Human chr19 - 11195760 11195749 11195761 AGACGTGGAAAGACAGGGAGAGAGACACGGAGAGAGACGCAGAAGGACAGAGACGTGGAGAGAGA AGACGTGGAAAGACAGGGAGAGAGACACGGA____________AGGACAGAGACGTGGAGAGAGA TTCTGCGTCTCTC T KANK2 Ensembl:ENSG00000197256 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:11195663..11195805 26863196 MeRIP-seq:(Medium) rs1394410264 Functional Loss DEL dbSNP153 32..43 33 - - - Human_Splice_Rec_1959550,Human_Splice_Rec_1959554 RMVar_hsa_circ_361073 81785 RMVar_ID_81785 Human_SNP_ID_658425945 m1A Human chr19 - 11197387 11197387 11197387 CACACACACCTACTACCCTACCCCCCGCCTCCAACCCTGGGACACGACCTCGCTGGTCTCAACGA CACACACACCTACTACCCTACCCCCCGCCTCCCACCCTGGGACACGACCTCGCTGGTCTCAACGA T G KANK2 Ensembl:ENSG00000197256 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11197383..11197525 26863196 MeRIP-seq:(Medium) rs888321031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19095870,Human_RBP_ID_22358882 81786 RMVar_ID_81786 Human_SNP_ID_658425946 m1A Human chr19 + 11197390 11197390 11197390 TTGAGACCAGCGAGGTCGTGTCCCAGGGTTGGAGGCGGGGGGTAGGGTAGTAGGTGTGTGTGGAG TTGAGACCAGCGAGGTCGTGTCCCAGGGTTGGGGGCGGGGGGTAGGGTAGTAGGTGTGTGTGGAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:11197381..11197524 26863196 MeRIP-seq:(Medium) rs1192948220 Functional Loss SNV dbSNP153 33..33 33 - - - 81787 RMVar_ID_81787 Human_SNP_ID_658427982 m1A Human chr19 - 11203677 11203677 11203677 CACTGTCTCTTAGTCTCTGTCTCTCCCTGCGTACCCAGCTTCCAGCCTCCCCCAGGCTCTCTGCT CACTGTCTCTTAGTCTCTGTCTCTCCCTGCGTCCCCAGCTTCCAGCCTCCCCCAGGCTCTCTGCT T G DOCK6 Ensembl:ENSG00000130158 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11203674..11203865 26863196 MeRIP-seq:(Medium) rs1457125127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2555917 RMVar_hsa_circ_85779,RMVar_hsa_circ_192546,RMVar_hsa_circ_78642,RMVar_hsa_circ_94713,RMVar_hsa_circ_192547,RMVar_hsa_circ_192548,RMVar_hsa_circ_91853,RMVar_hsa_circ_192549 81788 RMVar_ID_81788 Human_SNP_ID_658429835 m1A Human chr19 - 11209976 11209962 11209976 GGCAGGTGAGGGATGGGCAGGTGAGAGGGTGGACAGGTGAGGGCGGGCAGGTGAGAGGGTGGACA GGCAGGTGAGGGATGGGCAGGTGAGAGGGTGG______________GCAGGTGAGAGGGTGGACA CCCGCCCTCACCTGT C DOCK6 Ensembl:ENSG00000130158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11209974..11210089 26863196 MeRIP-seq:(Medium) rs1246243615 Functional Loss DEL dbSNP153 33..46 33 - - - RMVar_hsa_circ_56092,RMVar_hsa_circ_85779,RMVar_hsa_circ_192546,RMVar_hsa_circ_78642,RMVar_hsa_circ_94713,RMVar_hsa_circ_192547,RMVar_hsa_circ_192548,RMVar_hsa_circ_91853,RMVar_hsa_circ_343006,RMVar_hsa_circ_107849,RMVar_hsa_circ_192549,RMVar_hsa_circ_192550,RMVar_hsa_circ_370371,RMVar_hsa_circ_99435,RMVar_hsa_circ_109161,RMVar_hsa_circ_78242,RMVar_hsa_circ_192551,RMVar_hsa_circ_192553,RMVar_hsa_circ_192554,RMVar_hsa_circ_192555,RMVar_hsa_circ_192552,RMVar_hsa_circ_115369,RMVar_hsa_circ_192556 81789 RMVar_ID_81789 Human_SNP_ID_658430127 m1A Human chr19 - 11210810 11210810 11210810 TGGTGAAGAGATGGCCAGATGAGAAGATGAACAGGTGAGGAGGTGGACAGATAAGGAGACAGCTG TGGTGAAGAGATGGCCAGATGAGAAGATGAACGGGTGAGGAGGTGGACAGATAAGGAGACAGCTG T C DOCK6 Ensembl:ENSG00000130158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11210723..11211153 26863196 MeRIP-seq:(Medium) rs947894736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56092,RMVar_hsa_circ_85779,RMVar_hsa_circ_192546,RMVar_hsa_circ_78642,RMVar_hsa_circ_94713,RMVar_hsa_circ_192547,RMVar_hsa_circ_192548,RMVar_hsa_circ_91853,RMVar_hsa_circ_343006,RMVar_hsa_circ_107849,RMVar_hsa_circ_192549,RMVar_hsa_circ_192550,RMVar_hsa_circ_370371,RMVar_hsa_circ_99435,RMVar_hsa_circ_109161,RMVar_hsa_circ_78242,RMVar_hsa_circ_192551,RMVar_hsa_circ_192553,RMVar_hsa_circ_192554,RMVar_hsa_circ_192555,RMVar_hsa_circ_192552,RMVar_hsa_circ_115369,RMVar_hsa_circ_192556 81790 RMVar_ID_81790 Human_SNP_ID_658430175 m1A Human chr19 - 11210985 11210985 11210985 GGAAAAGGGTTGGACAGGCAGGTGAGTGGGTGAAGAAATGGACAGGTGAGGACACAAGTGAGGGG GGAAAAGGGTTGGACAGGCAGGTGAGTGGGTGTAGAAATGGACAGGTGAGGACACAAGTGAGGGG T A DOCK6 Ensembl:ENSG00000130158 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11210955..11211044 26863196 MeRIP-seq:(Medium) rs1172090426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56092,RMVar_hsa_circ_85779,RMVar_hsa_circ_192546,RMVar_hsa_circ_78642,RMVar_hsa_circ_94713,RMVar_hsa_circ_192547,RMVar_hsa_circ_192548,RMVar_hsa_circ_91853,RMVar_hsa_circ_343006,RMVar_hsa_circ_107849,RMVar_hsa_circ_192549,RMVar_hsa_circ_192550,RMVar_hsa_circ_370371,RMVar_hsa_circ_99435,RMVar_hsa_circ_109161,RMVar_hsa_circ_78242,RMVar_hsa_circ_192551,RMVar_hsa_circ_192553,RMVar_hsa_circ_192554,RMVar_hsa_circ_192555,RMVar_hsa_circ_192552,RMVar_hsa_circ_115369,RMVar_hsa_circ_192556 81791 RMVar_ID_81791 Human_SNP_ID_658431175 m1A Human chr19 - 11214368 11214368 11214368 CTTTCAGAAGCCCGGGAGAGCGTCTTGGGGGCAGTGCTGAAGGTTGTGCTGTACAGCCTGGGCAG CTTTCAGAAGCCCGGGAGAGCGTCTTGGGGGCGGTGCTGAAGGTTGTGCTGTACAGCCTGGGCAG T C DOCK6 Ensembl:ENSG00000130158 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11214318..11214562 32194978 MeRIP-seq:(Medium) rs895585948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512779,Human_RBP_ID_826418,Human_RBP_ID_910643,Human_RBP_ID_18996642 Human_Splice_Rec_1959634,Human_Splice_Rec_1959635,Human_Splice_Rec_1959690,Human_Splice_Rec_1959691 RMVar_hsa_circ_56092,RMVar_hsa_circ_78642,RMVar_hsa_circ_94713,RMVar_hsa_circ_192547,RMVar_hsa_circ_192548,RMVar_hsa_circ_91853,RMVar_hsa_circ_343006,RMVar_hsa_circ_107849,RMVar_hsa_circ_192549,RMVar_hsa_circ_192550,RMVar_hsa_circ_99435,RMVar_hsa_circ_109161,RMVar_hsa_circ_78242,RMVar_hsa_circ_80978,RMVar_hsa_circ_192551,RMVar_hsa_circ_192553,RMVar_hsa_circ_192554,RMVar_hsa_circ_192552,RMVar_hsa_circ_115369,RMVar_hsa_circ_192556,RMVar_hsa_circ_192559,RMVar_hsa_circ_123594,RMVar_hsa_circ_127886,RMVar_hsa_circ_78207,RMVar_hsa_circ_192560,RMVar_hsa_circ_67004,RMVar_hsa_circ_192558,RMVar_hsa_circ_95687,RMVar_hsa_circ_349087,RMVar_hsa_circ_369809,RMVar_hsa_circ_301703,RMVar_hsa_circ_92704,RMVar_hsa_circ_192561,RMVar_hsa_circ_192563,RMVar_hsa_circ_192564,RMVar_hsa_circ_192565,RMVar_hsa_circ_192562 81792 RMVar_ID_81792 Human_SNP_ID_658433689 m1A Human chr19 + 11222784 11222782 11222785 ACACAGAGGGGGAGGGCGAGGCTGGAGGTGACAGGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG ACACAGAGGGGGAGGGCGAGGCTGGAGGTGA___GGGGCAGCAGGGGAGGTTGAGGGTCACGTAG ACAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:11222695..11222852;chr19:11222759..11222848 26863196 MeRIP-seq:(Medium) rs1555691141 Functional Loss DEL dbSNP153 32..34 33 - - - 81793 RMVar_ID_81793 Human_SNP_ID_658433690 m1A Human chr19 + 11222784 11222783 11222785 ACACAGAGGGGGAGGGCGAGGCTGGAGGTGACAGGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG ACACAGAGGGGGAGGGCGAGGCTGGAGGTGAC__GGGGCAGCAGGGGAGGTTGAGGGTCACGTAG CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:11222695..11222852;chr19:11222759..11222848 26863196 MeRIP-seq:(Medium) rs747575528 Functional Loss DEL dbSNP153 33..34 33 - - - 81794 RMVar_ID_81794 Human_SNP_ID_658433691 m1A Human chr19 + 11222784 11222783 11222784 ACACAGAGGGGGAGGGCGAGGCTGGAGGTGACAGGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG ACACAGAGGGGGAGGGCGAGGCTGGAGGTGAC_GGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:11222695..11222852;chr19:11222759..11222848 26863196 MeRIP-seq:(Medium) rs891568939 Functional Loss DEL dbSNP153 33..33 33 - - - 81795 RMVar_ID_81795 Human_SNP_ID_658433692 m1A Human chr19 + 11222784 11222784 11222784 ACACAGAGGGGGAGGGCGAGGCTGGAGGTGACAGGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG ACACAGAGGGGGAGGGCGAGGCTGGAGGTGACGGGGGGCAGCAGGGGAGGTTGAGGGTCACGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:11222695..11222852;chr19:11222759..11222848 26863196 MeRIP-seq:(Medium) rs370735885 Functional Loss SNV dbSNP153 33..33 33 - - - 81796 RMVar_ID_81796 Human_SNP_ID_658438089 m1A Human chr19 + 11238296 11238291 11238296 TGCTGAAGTTGAGGCTGTGCGGGTACACGTACAGCAGGTTCCTGTGGGGGGCAGGATGGGGGTGT TGCTGAAGTTGAGGCTGTGCGGGTACAC_____GCAGGTTCCTGTGGGGGGCAGGATGGGGGTGT CGTACA C ANGPTL8 Ensembl:ENSG00000130173 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11238273..11239708 32194978 MeRIP-seq:(Medium) rs1485689792 Functional Loss DEL dbSNP153 29..33 33 - - - 81797 RMVar_ID_81797 Human_SNP_ID_658438938 m1A Human chr19 + 11241421 11241421 11241421 CAGGGGATGGGAGGTGAGGTGGCTGTCGGCTGAGGTTTCCATTCTGACCCCCACAGGCTCACGCT CAGGGGATGGGAGGTGAGGTGGCTGTCGGCTGCGGTTTCCATTCTGACCCCCACAGGCTCACGCT A C ANGPTL8 Ensembl:ENSG00000130173 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11241417..11241516 26863196 MeRIP-seq:(Medium) rs1441638165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908461,Human_RBP_ID_9425201,Human_RBP_ID_22545644,Human_RBP_ID_26785322 81798 RMVar_ID_81798 Human_SNP_ID_658445215 m1A Human chr19 - 11262361 11262361 11262361 GTGTGGCCGCGGGGCCCCCTCCCACCTCCCCCACGTGGCCCGGCTCCGCCCCGGGGCGGTGCGAC GTGTGGCCGCGGGGCCCCCTCCCACCTCCCCCCCGTGGCCCGGCTCCGCCCCGGGGCGGTGCGAC T G DOCK6 Ensembl:ENSG00000130158 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11262359..11262474 26863196 MeRIP-seq:(Medium) rs1489589399 Functional Loss SNV dbSNP153 33..33 33 - - - 81799 RMVar_ID_81799 Human_SNP_ID_658445253 m1A Human chr19 - 11262443 11262443 11262443 GGGGCCCGGGGCGGCGGCGGCGGGACGCGAGGACCATGGCTGCCTCCGAGCGCCGCGCCTTCGCG GGGGCCCGGGGCGGCGGCGGCGGGACGCGAGGTCCATGGCTGCCTCCGAGCGCCGCGCCTTCGCG T A DOCK6 Ensembl:ENSG00000130158 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11262374..11262484 26863196 MeRIP-seq:(Medium) rs759309200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1959569,Human_Splice_Rec_1959761 81800 RMVar_ID_81800 Human_SNP_ID_658468172 m1A Human chr19 - 11345583 11345583 11345583 AGGAAGGCGGGAACCTAGGAGGCCTGATTAAGATGGTCCATCTACTGGTCTTGTCAGGTGCCTGG AGGAAGGCGGGAACCTAGGAGGCCTGATTAAGGTGGTCCATCTACTGGTCTTGTCAGGTGCCTGG T C RAB3D,TMEM205 Ensembl:ENSG00000105514,Ensembl:ENSG00000105518 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11345509..11345687 26863196 MeRIP-seq:(Medium) rs1386532454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512817,Human_RBP_ID_1012923,Human_RBP_ID_4557231,Human_RBP_ID_22447409,Human_RBP_ID_23781641 Human_Splice_Rec_1959890,Human_Splice_Rec_1959891,Human_Splice_Rec_1959896,Human_Splice_Rec_1959897,Human_Splice_Rec_1959903,Human_Splice_Rec_1959908,Human_Splice_Rec_1959909,Human_Splice_Rec_1959915,Human_Splice_Rec_1959921,Human_Splice_Rec_1959926,Human_Splice_Rec_1959927,Human_Splice_Rec_1959933,Human_Splice_Rec_1959944,Human_Splice_Rec_1959945,Human_Splice_Rec_1959947,Human_Splice_Rec_1959952,Human_Splice_Rec_1959953,Human_Splice_Rec_1959958,Human_Splice_Rec_1959959 RMVar_hsa_circ_86673,RMVar_hsa_circ_102892,RMVar_hsa_circ_192581,RMVar_hsa_circ_192582,RMVar_hsa_circ_329344 81801 RMVar_ID_81801 Human_SNP_ID_658468185 m1A Human chr19 + 11345625 11345625 11345625 GCCTCCTAGGTTCCCGCCTTCCTCCATCTTGCAGTCCTGGGAAGGAGGCACCGGGTGGCTCAGAA GCCTCCTAGGTTCCCGCCTTCCTCCATCTTGCGGTCCTGGGAAGGAGGCACCGGGTGGCTCAGAA A G CCDC159 Ensembl:ENSG00000183401 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11345204..11345739 26863196 MeRIP-seq:(Medium) rs751181928 Functional Loss SNV dbSNP153 33..33 33 - - - 81802 RMVar_ID_81802 Human_SNP_ID_658468278 m1A Human chr19 + 11346062 11346062 11346062 AAAGCCCCGAGGAAACCCTAAATCTCATCCTGAGGACACCGATCCCACCAAAGCCCCGAGGAAAC AAAGCCCCGAGGAAACCCTAAATCTCATCCTGTGGACACCGATCCCACCAAAGCCCCGAGGAAAC A T CCDC159 Ensembl:ENSG00000183401 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11346059..11346206 32194978 MeRIP-seq:(Medium) rs945900038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1959964 81803 RMVar_ID_81803 Human_SNP_ID_658468320 m1A Human chr19 - 11346244 11346244 11346244 GGTTGGGGGAAACCCACGAGGGGACGCGGCCGAGGAGGGTCGCTGTCCACCCGGGGGCGTGGGAG GGTTGGGGGAAACCCACGAGGGGACGCGGCCGCGGAGGGTCGCTGTCCACCCGGGGGCGTGGGAG T G RAB3D,TMEM205 Ensembl:ENSG00000105514,Ensembl:ENSG00000105518 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11346087..11346275 26863196 MeRIP-seq:(Medium) rs1378969436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137674,Human_RBP_ID_239794,Human_RBP_ID_770894,Human_RBP_ID_4500726,Human_RBP_ID_5320172,Human_RBP_ID_17934871,Human_RBP_ID_18421269 Human_Splice_Rec_1959907,Human_Splice_Rec_1959919,Human_Splice_Rec_1959939,Human_Splice_Rec_1959943 RMVar_hsa_circ_102892,RMVar_hsa_circ_192581 81804 RMVar_ID_81804 Human_SNP_ID_658470364 m1A Human chr19 - 11353593 11353593 11353593 GGGGGAACGGGTTCAGAGGAGGGTCAGGGGTCAGACTGCAGGCTGGGCATCACCATATATCACTC GGGGGAACGGGTTCAGAGGAGGGTCAGGGGTCCGACTGCAGGCTGGGCATCACCATATATCACTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11353544..11353793 26863196 MeRIP-seq:(Medium) rs369266931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6718669 81805 RMVar_ID_81805 Human_SNP_ID_658471351 m1A Human chr19 - 11357077 11357077 11357077 CCTTCCCCCTCTTCCCAGCCGGTCTGCCTCCCAGTTCTCCTCTTCCCTCCCCCAAGGCTACCCCC CCTTCCCCCTCTTCCCAGCCGGTCTGCCTCCCGGTTCTCCTCTTCCCTCCCCCAAGGCTACCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11357075..11357172 26863196 MeRIP-seq:(Medium) rs1266925560 Functional Loss SNV dbSNP153 33..33 33 - - - 81806 RMVar_ID_81806 Human_SNP_ID_658472645 m1A Human chr19 + 11361485 11361485 11361485 GCGGCCCTCTGCGCCTACGCGGTCACCTACACAGCGGTGAGCTTCGGGAGCTTCGGGGTCGGAAA GCGGCCCTCTGCGCCTACGCGGTCACCTACACGGCGGTGAGCTTCGGGAGCTTCGGGGTCGGAAA A G PLPPR2 Ensembl:ENSG00000105520 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11361437..11362561 32194978 MeRIP-seq:(Medium) rs764064012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512822,Human_RBP_ID_27463177 Human_Splice_Rec_1960145,Human_Splice_Rec_1960183,Human_Splice_Rec_1960195,Human_Splice_Rec_1960199 RMVar_hsa_circ_116024,RMVar_hsa_circ_114982,RMVar_hsa_circ_192588,RMVar_hsa_circ_9843,RMVar_hsa_circ_192590 81807 RMVar_ID_81807 Human_SNP_ID_658473421 m1A Human chr19 + 11364190 11364190 11364190 CAGGAACCCGAGGTCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAGTGAGTGTTG CAGGAACCCGAGGTCTGCAGGCCGCATTCGACCCCGGCACGGCTCACCCCATCCAGTGAGTGTTG A C PLPPR2 Ensembl:ENSG00000105520 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11364178..11364558 32194978 MeRIP-seq:(Medium) rs747832383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907363,Human_RBP_ID_19089319 Human_Splice_Rec_1960150,Human_Splice_Rec_1960151,Human_Splice_Rec_1960188,Human_Splice_Rec_1960189 RMVar_hsa_circ_116024,RMVar_hsa_circ_114982,RMVar_hsa_circ_192588,RMVar_hsa_circ_192590,RMVar_hsa_circ_192591,RMVar_hsa_circ_19375 81808 RMVar_ID_81808 Human_SNP_ID_658473422 m1A Human chr19 + 11364190 11364190 11364190 CAGGAACCCGAGGTCTGCAGGCCGCATTCGACACCGGCACGGCTCACCCCATCCAGTGAGTGTTG CAGGAACCCGAGGTCTGCAGGCCGCATTCGACGCCGGCACGGCTCACCCCATCCAGTGAGTGTTG A G PLPPR2 Ensembl:ENSG00000105520 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11364178..11364558 32194978 MeRIP-seq:(Medium) rs747832383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907363,Human_RBP_ID_19089319 Human_Splice_Rec_1960150,Human_Splice_Rec_1960151,Human_Splice_Rec_1960188,Human_Splice_Rec_1960189 RMVar_hsa_circ_116024,RMVar_hsa_circ_114982,RMVar_hsa_circ_192588,RMVar_hsa_circ_192590,RMVar_hsa_circ_192591,RMVar_hsa_circ_19375 81809 RMVar_ID_81809 Human_SNP_ID_658476188 m1A Human chr19 - 11374694 11374694 11374694 AGGCCGCACCGCCCCTGGTTAGCACCCGCCTCAGCGTCTCCGCCATTCGCCGCGTAGCTCTGACC AGGCCGCACCGCCCCTGGTTAGCACCCGCCTCGGCGTCTCCGCCATTCGCCGCGTAGCTCTGACC T C AC024575.2 Ensembl:ENSG00000267277 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11374686..11374834 26863196 MeRIP-seq:(Medium) rs1250505894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1960203 81810 RMVar_ID_81810 Human_SNP_ID_658478118 m1A Human chr19 + 11380945 11380945 11380945 CAGCAGCACCAGGATGACCACGAGGATGAGGGAGAGCGTCAGGATGAGGGGGTCCAGGTCTAAGA CAGCAGCACCAGGATGACCACGAGGATGAGGGGGAGCGTCAGGATGAGGGGGTCCAGGTCTAAGA A G NONHSAG024835.2 RNACentral:URS00008C16D6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11380895..11381104 26863196 MeRIP-seq:(Medium) rs1459614745 Functional Loss SNV dbSNP153 33..33 33 - - - 81811 RMVar_ID_81811 Human_SNP_ID_658479107 m1A Human chr19 - 11383355 11383355 11383355 TCTGCGGACCCCTCCAAGGGACCCGCTTGGGAAGATGGCAGGGCGGGGCTTTTTTCTTATCGGGT TCTGCGGACCCCTCCAAGGGACCCGCTTGGGACGATGGCAGGGCGGGGCTTTTTTCTTATCGGGT T G EPOR Ensembl:ENSG00000187266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11383352..11383464 26863196 MeRIP-seq:(Medium) rs1339785771 Functional Loss SNV dbSNP153 33..33 33 - - - 81812 RMVar_ID_81812 Human_SNP_ID_658482396 m1A Human chr19 + 11394558 11394558 11394558 CAGGAGTGGAGATGGTGGTAATAGGCCCTCACAACCTTGTGTCACCCCCACAGAGGACCCGGGAG CAGGAGTGGAGATGGTGGTAATAGGCCCTCACGACCTTGTGTCACCCCCACAGAGGACCCGGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11394539..11394627 26863196 MeRIP-seq:(Medium) rs1260687325 Functional Loss SNV dbSNP153 33..33 33 - - - 81813 RMVar_ID_81813 Human_SNP_ID_658482424 m1A Human chr19 + 11394649 11394649 11394649 AACAGCCATGGGTCCCTCTGCAGCTACTGCCAAGCCAAGCTCATTCTGCTGTCACTGGGAACCTG AACAGCCATGGGTCCCTCTGCAGCTACTGCCAGGCCAAGCTCATTCTGCTGTCACTGGGAACCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11394641..11394718 26863196 MeRIP-seq:(Medium) rs1444003421 Functional Loss SNV dbSNP153 33..33 33 - - - 81814 RMVar_ID_81814 Human_SNP_ID_658482609 m1A Human chr19 + 11395302 11395302 11395302 TCCAGCCTGCACGAGCTTGTGGCCTCACACTCAACACCTGAACAACCACAAGCATCCTTTCCTAA TCCAGCCTGCACGAGCTTGTGGCCTCACACTCGACACCTGAACAACCACAAGCATCCTTTCCTAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11395264..11395460 26863196 MeRIP-seq:(Medium) rs917765259 Functional Loss SNV dbSNP153 33..33 33 - - - 81815 RMVar_ID_81815 Human_SNP_ID_658482634 m1A Human chr19 + 11395415 11395415 11395415 CCTTGCTTCTCCCTGTCAGACAGGACAATCTCATGCTTCCGCGGCTATCCATTTGCCTCTCTCCC CCTTGCTTCTCCCTGTCAGACAGGACAATCTCTTGCTTCCGCGGCTATCCATTTGCCTCTCTCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11395191..11395436 26863196 MeRIP-seq:(Medium) rs181153141 Functional Loss SNV dbSNP153 33..33 33 - - - 81816 RMVar_ID_81816 Human_SNP_ID_658483403 m1A Human chr19 - 11397458 11397458 11397458 CGTCAGCATCGACAATGACCACGGGAACCTGTATCGAAGCATCTTGGTGAGGGGCTGGGCTGGGG CGTCAGCATCGACAATGACCACGGGAACCTGTGTCGAAGCATCTTGGTGAGGGGCTGGGCTGGGG T C RGL3 Ensembl:ENSG00000205517 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11397292..11397627 32194978 MeRIP-seq:(Medium) rs147520409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585325,Human_RBP_ID_18996689 Human_Splice_Rec_1960343,Human_Splice_Rec_1960381,Human_Splice_Rec_1960405,Human_Splice_Rec_1960441,Human_Splice_Rec_1960445,Human_Splice_Rec_1960483,Human_Splice_Rec_1960487 RMVar_hsa_circ_8935,RMVar_hsa_circ_329168,RMVar_hsa_circ_192592 81817 RMVar_ID_81817 Human_SNP_ID_658484242 m1A Human chr19 - 11400270 11400270 11400270 CTCAGCTACCGGCTCTCCCGGGTCATTGAGCCACCAGCTGCCTCCTGCCCCAGCTCCCCACGCAT CTCAGCTACCGGCTCTCCCGGGTCATTGAGCCGCCAGCTGCCTCCTGCCCCAGCTCCCCACGCAT T C RGL3 Ensembl:ENSG00000205517 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11400141..11400323 26863196 MeRIP-seq:(Medium) rs1270326742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25441276 Human_Splice_Rec_1960336,Human_Splice_Rec_1960337,Human_Splice_Rec_1960374,Human_Splice_Rec_1960375,Human_Splice_Rec_1960398,Human_Splice_Rec_1960399,Human_Splice_Rec_1960434,Human_Splice_Rec_1960435,Human_Splice_Rec_1960476,Human_Splice_Rec_1960477 RMVar_hsa_circ_8935,RMVar_hsa_circ_36952,RMVar_hsa_circ_46089 81818 RMVar_ID_81818 Human_SNP_ID_658484905 m1A Human chr19 - 11402407 11402407 11402407 CTTGACCCCTGACCCCAGCTCCACTTGCCCCCAGCACAATGGGCCTCCCAATATCCACCCTTGAT CTTGACCCCTGACCCCAGCTCCACTTGCCCCCGGCACAATGGGCCTCCCAATATCCACCCTTGAT T C RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11402360..11402592 26863196 MeRIP-seq:(Medium) rs767684769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17081723,Human_RBP_ID_19089322 RMVar_hsa_circ_8935,RMVar_hsa_circ_18342 81819 RMVar_ID_81819 Human_SNP_ID_658484955 m1A Human chr19 + 11402524 11402524 11402524 AGGTCCGTAAGGAAGGTGCCAAGGTAGGGGACAGGGCCTGGGGGTGGTTTCTGCAGCCCCCAAAG AGGTCCGTAAGGAAGGTGCCAAGGTAGGGGACGGGGCCTGGGGGTGGTTTCTGCAGCCCCCAAAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11402428..11402528 32194978 MeRIP-seq:(Medium) rs1333034659 Functional Loss SNV dbSNP153 33..33 33 - - - 81820 RMVar_ID_81820 Human_SNP_ID_658486026 m1A Human chr19 - 11406125 11406125 11406125 GCAGCTGGGGAGGGGCTGGAGCCCGAGGGAGGAGGGAGGAAGGGAATCCTAGGGAATAAGTGGGA GCAGCTGGGGAGGGGCTGGAGCCCGAGGGAGGGGGGAGGAAGGGAATCCTAGGGAATAAGTGGGA T C RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11406121..11406250 26863196 MeRIP-seq:(Medium) rs545260793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313692 81821 RMVar_ID_81821 Human_SNP_ID_658489641 m1A Human chr19 - 11416747 11416747 11416747 CCCCTCCACCTCCTCAGGTGTGGAACCTGGAAACACCTCCCAGACCCAGAGCCCTCTTCCTAAGC CCCCTCCACCTCCTCAGGTGTGGAACCTGGAAGCACCTCCCAGACCCAGAGCCCTCTTCCTAAGC T C RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11416738..11416843 26863196 MeRIP-seq:(Medium) rs781124268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46114,RMVar_hsa_circ_313692,RMVar_hsa_circ_325593,RMVar_hsa_circ_274391,RMVar_hsa_circ_192593,RMVar_hsa_circ_312377 81822 RMVar_ID_81822 Human_SNP_ID_658490203 m1A Human chr19 + 11418311 11418311 11418311 CAGGGCTTCCCTCAGCCCTCCTGTCGCGCTTCACTGGCTGCCCCATCCGCCCTCACCTAGCCACT CAGGGCTTCCCTCAGCCCTCCTGTCGCGCTTCTCTGGCTGCCCCATCCGCCCTCACCTAGCCACT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11418309..11418475 26863196 MeRIP-seq:(Medium) rs912050642 Functional Loss SNV dbSNP153 33..33 33 - - - 81823 RMVar_ID_81823 Human_SNP_ID_658494733 m1A Human chr19 + 11426937 11426937 11426937 CCGCCATCTCCAGAAGGCGCAGGCTGTGCTGCAGCTGGAGCTCCTCCAGCCGCCTCTGCCGCAAC CCGCCATCTCCAGAAGGCGCAGGCTGTGCTGCTGCTGGAGCTCCTCCAGCCGCCTCTGCCGCAAC A T NONHSAG024840.2 RNACentral:URS00009B3BDB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11426930..11427078 26863196 MeRIP-seq:(Medium) rs949344451 Functional Loss SNV dbSNP153 33..33 33 - - - 81824 RMVar_ID_81824 Human_SNP_ID_658495877 m1A Human chr19 + 11430664 11430663 11430664 CTGGAGTCCAGTGGTGAGGGGACCCAGGCTGGAAATGAAGGAGGAGGTGGGGCGAGGGTGGGCAA CTGGAGTCCAGTGGTGAGGGGACCCAGGCTGG_AATGAAGGAGGAGGTGGGGCGAGGGTGGGCAA GA G NONHSAG024840.2 RNACentral:URS00009B3BDB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11430654..11430763 26863196 MeRIP-seq:(Medium) rs780207674 Functional Loss DEL dbSNP153 33..33 33 - - - 81825 RMVar_ID_81825 Human_SNP_ID_658495963 m1A Human chr19 + 11430865 11430865 11430865 TGCTACCTACTTGTCCCCCACCATCCACCGCCACGGGAACCCTACACCCACCCCTTTGCCCCTTA TGCTACCTACTTGTCCCCCACCATCCACCGCCGCGGGAACCCTACACCCACCCCTTTGCCCCTTA A G NONHSAG024840.2 RNACentral:URS00009B3BDB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11430861..11430947 26863196 MeRIP-seq:(Medium) rs34095 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - 81826 RMVar_ID_81826 Human_SNP_ID_658497459 m1A Human chr19 - 11435696 11435696 11435696 CCACCCGCTCGTTCACACCTACACGAGGCCGGAGCAAAGGTCAGTATCCACCGCACCCCTCTTGT CCACCCGCTCGTTCACACCTACACGAGGCCGGGGCAAAGGTCAGTATCCACCGCACCCCTCTTGT T C CCDC151 Ensembl:ENSG00000198003 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:11435626..11435772;chr19:11435626..11435725 26863196 MeRIP-seq:(Medium) rs992982896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1960629 81827 RMVar_ID_81827 Human_SNP_ID_658497631 m1A Human chr19 - 11436125 11436125 11436125 CCCAGCACATGGGTAGCAGCAGCAGCAGCGGCAACAGCATCTCACCAGACGCTCTGAGGCCCGAA CCCAGCACATGGGTAGCAGCAGCAGCAGCGGCGACAGCATCTCACCAGACGCTCTGAGGCCCGAA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11436076..11436125 26863196 MeRIP-seq:(Medium) rs113268712 Functional Loss SNV dbSNP153 33..33 33 - - - 81828 RMVar_ID_81828 Human_SNP_ID_658497678 m1A Human chr19 + 11436196 11436196 11436196 AGGTCAAGAGGCCCCGGGGCGTCTCCCTCACCAGTGAGTCCTCCTGTTCACCCTCCCGCCAGGCT AGGTCAAGAGGCCCCGGGGCGTCTCCCTCACCCGTGAGTCCTCCTGTTCACCCTCCCGCCAGGCT A C PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11436026..11436200 32194978 MeRIP-seq:(Medium) rs751480382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557238,Human_RBP_ID_5145044,Human_RBP_ID_22448386 Human_Splice_Rec_1960661,Human_Splice_Rec_1960695,Human_Splice_Rec_1960699,Human_Splice_Rec_1960715,Human_Splice_Rec_1960725,Human_Splice_Rec_1960735,Human_Splice_Rec_1960745,Human_Splice_Rec_1960779,Human_Splice_Rec_1960787,Human_Splice_Rec_1960819 RMVar_hsa_circ_2923,RMVar_hsa_circ_23741 81829 RMVar_ID_81829 Human_SNP_ID_658497782 m1A Human chr19 - 11436393 11436393 11436393 CAGGTGAAAGGCTTGGACTCATCGTAGAAGTGATGATCTGCGGGGTACAGGAAGCTCAGCCCAGG CAGGTGAAAGGCTTGGACTCATCGTAGAAGTGCTGATCTGCGGGGTACAGGAAGCTCAGCCCAGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11436376..11436450 26863196 MeRIP-seq:(Medium) rs779747276 Functional Loss SNV dbSNP153 33..33 33 - - - 81830 RMVar_ID_81830 Human_SNP_ID_658498395 m1A Human chr19 + 11438123 11438123 11438123 ACAACAGCGGCGTCATCTGTGAGAACACCTGCAAGTACGTGGGTGACAGTACCCCTCCCATCACC ACAACAGCGGCGTCATCTGTGAGAACACCTGCCAGTACGTGGGTGACAGTACCCCTCCCATCACC A C PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11437876..11438125 26863196 MeRIP-seq:(Medium) rs746717003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22762755 Human_Splice_Rec_1960666,Human_Splice_Rec_1960667,Human_Splice_Rec_1960704,Human_Splice_Rec_1960705,Human_Splice_Rec_1960720,Human_Splice_Rec_1960721,Human_Splice_Rec_1960730,Human_Splice_Rec_1960731,Human_Splice_Rec_1960740,Human_Splice_Rec_1960741,Human_Splice_Rec_1960750,Human_Splice_Rec_1960751,Human_Splice_Rec_1960784,Human_Splice_Rec_1960785,Human_Splice_Rec_1960792,Human_Splice_Rec_1960793,Human_Splice_Rec_1960824,Human_Splice_Rec_1960825 RMVar_hsa_circ_23741,RMVar_hsa_circ_192594,RMVar_hsa_circ_284254 81831 RMVar_ID_81831 Human_SNP_ID_658498397 m1A Human chr19 - 11438126 11438126 11438126 TGGGGTGATGGGAGGGGTACTGTCACCCACGTACTTGCAGGTGTTCTCACAGATGACGCCGCTGT TGGGGTGATGGGAGGGGTACTGTCACCCACGTCCTTGCAGGTGTTCTCACAGATGACGCCGCTGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr19:11438076..11438125 26863196,32194978 MeRIP-seq:(Medium) rs112604914 Functional Loss SNV dbSNP153 33..33 33 - - - 81832 RMVar_ID_81832 Human_SNP_ID_658499761 m1A Human chr19 + 11442399 11442399 11442399 TTGCCTTCTGCCCACCCAGAAAAAGCTCATTGAGCTACAGGCTGGGAAGAAGTCTCTGGAAGACC TTGCCTTCTGCCCACCCAGAAAAAGCTCATTGGGCTACAGGCTGGGAAGAAGTCTCTGGAAGACC A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11442376..11442400 26863196 MeRIP-seq:(Medium) rs1310448812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53856,Human_RBP_ID_912562,Human_RBP_ID_1012927,Human_RBP_ID_3954514,Human_RBP_ID_5585330,Human_RBP_ID_8476834,Human_RBP_ID_9380544,Human_RBP_ID_17655518,Human_RBP_ID_18996702,Human_RBP_ID_22762760,Human_RBP_ID_26335749,Human_RBP_ID_26982347,Human_RBP_ID_27815156 Human_Splice_Rec_1960670,Human_Splice_Rec_1960708,Human_Splice_Rec_1960754,Human_Splice_Rec_1960796,Human_Splice_Rec_1960828 RMVar_hsa_circ_88582,RMVar_hsa_circ_192595,RMVar_hsa_circ_346963,RMVar_hsa_circ_192596 81833 RMVar_ID_81833 Human_SNP_ID_658499769 m1A Human chr19 + 11442432 11442432 11442432 GCTACAGGCTGGGAAGAAGTCTCTGGAAGACCAGGTGGAGATGCTGCGGACAGTGAAGGAGGAAG GCTACAGGCTGGGAAGAAGTCTCTGGAAGACCGGGTGGAGATGCTGCGGACAGTGAAGGAGGAAG A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:11442376..11442525 26863196 MeRIP-seq:(Medium) rs1460548929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53856,Human_RBP_ID_825091,Human_RBP_ID_912562,Human_RBP_ID_1187188,Human_RBP_ID_1879875,Human_RBP_ID_3562694,Human_RBP_ID_3954515,Human_RBP_ID_5117352,Human_RBP_ID_5469453,Human_RBP_ID_5585330,Human_RBP_ID_6718705,Human_RBP_ID_8476835,Human_RBP_ID_9380544,Human_RBP_ID_17655518,Human_RBP_ID_18191980,Human_RBP_ID_18996702,Human_RBP_ID_22446441,Human_RBP_ID_22762760,Human_RBP_ID_26335749,Human_RBP_ID_27815157 Human_Splice_Rec_1960670,Human_Splice_Rec_1960671,Human_Splice_Rec_1960708,Human_Splice_Rec_1960754,Human_Splice_Rec_1960755,Human_Splice_Rec_1960796,Human_Splice_Rec_1960797,Human_Splice_Rec_1960828,Human_Splice_Rec_1960829,Human_Splice_Rec_1960851 Human_miRNA_ID_1938440,Human_miRNA_ID_1938441,Human_miRNA_ID_1949540,Human_miRNA_ID_1949541 GWAS_ID_9619,GWAS_ID_9620 RMVar_hsa_circ_192597,RMVar_hsa_circ_88582,RMVar_hsa_circ_192595,RMVar_hsa_circ_346963,RMVar_hsa_circ_192596,RMVar_hsa_circ_379029 81834 RMVar_ID_81834 Human_SNP_ID_658499772 m1A Human chr19 - 11442441 11442441 11442441 GCTTCTCAGCTTCCTCCTTCACTGTCCGCAGCATCTCCACCTGGTCTTCCAGAGACTTCTTCCCA GCTTCTCAGCTTCCTCCTTCACTGTCCGCAGCGTCTCCACCTGGTCTTCCAGAGACTTCTTCCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11441075..11445508 32194978 MeRIP-seq:(Medium) rs756794365 Functional Loss SNV dbSNP153 33..33 33 - - - 81835 RMVar_ID_81835 Human_SNP_ID_658500616 m1A Human chr19 - 11445379 11445377 11445380 GGCCTTGGCAGCAGCCAGCTGCTCTGTAAAGAAGCCACCTCTGTCACCCCCTGCCCACCCACCGG GGCCTTGGCAGCAGCCAGCTGCTCTGTAAAG___CCACCTCTGTCACCCCCTGCCCACCCACCGG GCTT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11445376..11445475 26863196 MeRIP-seq:(Medium) rs1420847651 Functional Loss DEL dbSNP153 32..34 33 - - - 81836 RMVar_ID_81836 Human_SNP_ID_658500640 m1A Human chr19 - 11445442 11445442 11445442 CGTCCCGTCCATGTCATCATCCAGCTCCTTGAAGGCATCAGCCGCCAGCTCCTGCTCCTGTTGGG CGTCCCGTCCATGTCATCATCCAGCTCCTTGAGGGCATCAGCCGCCAGCTCCTGCTCCTGTTGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11445344..11445539 26863196 MeRIP-seq:(Medium) rs376748469 Functional Loss SNV dbSNP153 33..33 33 - - - 81837 RMVar_ID_81837 Human_SNP_ID_658501253 m1A Human chr19 - 11447162 11447162 11447162 GAGGACCAAGTCCCCTCCCTTCTCCTCCACTGACCTCGGACCGGTACTTGTCCCTGATGGCGGCC GAGGACCAAGTCCCCTCCCTTCTCCTCCACTGGCCTCGGACCGGTACTTGTCCCTGATGGCGGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11447151..11447175 26863196 MeRIP-seq:(Medium) rs113088622 Functional Loss SNV dbSNP153 33..33 33 - - - 81838 RMVar_ID_81838 Human_SNP_ID_658501396 m1A Human chr19 + 11447525 11447525 11447525 GAGGAGCAGCCGCCAGTGCCCTCGTCGCCCACAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGA GAGGAGCAGCCGCCAGTGCCCTCGTCGCCCACGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGA A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11447476..11447525 26863196 MeRIP-seq:(Medium) rs1294882349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22762772,Human_RBP_ID_25382967 Human_Splice_Rec_1960678,Human_Splice_Rec_1960679,Human_Splice_Rec_1960762,Human_Splice_Rec_1960763,Human_Splice_Rec_1960804,Human_Splice_Rec_1960805,Human_Splice_Rec_1960836,Human_Splice_Rec_1960837,Human_Splice_Rec_1960856,Human_Splice_Rec_1960857,Human_Splice_Rec_1960860,Human_Splice_Rec_1960862,Human_Splice_Rec_1960863,Human_Splice_Rec_1960867 RMVar_hsa_circ_21009,RMVar_hsa_circ_192598,RMVar_hsa_circ_371287,RMVar_hsa_circ_59117 81839 RMVar_ID_81839 Human_SNP_ID_658501527 m1A Human chr19 + 11447729 11447729 11447729 CCCCACCGCCACTGTCACCCCCGCAGCCGGCCAGCCCTGCTGAGGAAGACAAAATGCCGCCCTAC CCCCACCGCCACTGTCACCCCCGCAGCCGGCCGGCCCTGCTGAGGAAGACAAAATGCCGCCCTAC A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:11447413..11447844;chr19:11447415..11447821 26863196 MeRIP-seq:(Medium) rs570742302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512900,Human_RBP_ID_913826,Human_RBP_ID_3954519,Human_RBP_ID_17656762,Human_RBP_ID_22447424,Human_RBP_ID_22762776,Human_RBP_ID_24545717,Human_RBP_ID_26335757 Human_Splice_Rec_1960680,Human_Splice_Rec_1960681,Human_Splice_Rec_1960764,Human_Splice_Rec_1960765,Human_Splice_Rec_1960806,Human_Splice_Rec_1960807,Human_Splice_Rec_1960838,Human_Splice_Rec_1960839,Human_Splice_Rec_1960858,Human_Splice_Rec_1960864,Human_Splice_Rec_1960865,Human_Splice_Rec_1960868,Human_Splice_Rec_1960869 Human_miRNA_ID_599712,Human_miRNA_ID_1046163,Human_miRNA_ID_2223807,Human_miRNA_ID_2486876,Human_miRNA_ID_2999810,Human_miRNA_ID_3075241 RMVar_hsa_circ_192598,RMVar_hsa_circ_371287 81840 RMVar_ID_81840 Human_SNP_ID_658501561 m1A Human chr19 - 11447791 11447791 11447791 CCACCCGAGGAGCCTGGCCCCCGCCCACCCTCACCATCGATGAAGGCCTGCGTCTGCTCGTCGTA CCACCCGAGGAGCCTGGCCCCCGCCCACCCTCTCCATCGATGAAGGCCTGCGTCTGCTCGTCGTA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11447718..11447819 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81841 RMVar_ID_81841 Human_SNP_ID_658501562 m1A Human chr19 - 11447791 11447791 11447791 CCACCCGAGGAGCCTGGCCCCCGCCCACCCTCACCATCGATGAAGGCCTGCGTCTGCTCGTCGTA CCACCCGAGGAGCCTGGCCCCCGCCCACCCTCCCCATCGATGAAGGCCTGCGTCTGCTCGTCGTA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11447718..11447819 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 81842 RMVar_ID_81842 Human_SNP_ID_658501692 m1A Human chr19 - 11448188 11448188 11448188 TGGGAGAGGGGTTGGAGGTCAGAGATGTCCTCAACCCCATCCAGGAGGATGGGGAACGGGGTTCC TGGGAGAGGGGTTGGAGGTCAGAGATGTCCTCCACCCCATCCAGGAGGATGGGGAACGGGGTTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11448186..11448346 26863196 MeRIP-seq:(Medium) rs1234843969 Functional Loss SNV dbSNP153 33..33 33 - - - 81843 RMVar_ID_81843 Human_SNP_ID_658502108 m1A Human chr19 - 11449177 11449175 11449177 CCCGCCCCAGCTCCCCTGCCTTGCAGGCACTCACGGTGGTGGAGCGGTTGGGGCCCTGCCAGCAG CCCGCCCCAGCTCCCCTGCCTTGCAGGCACTC__GGTGGTGGAGCGGTTGGGGCCCTGCCAGCAG CGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11449126..11449200 26863196 MeRIP-seq:(Medium) rs757957327 Functional Loss DEL dbSNP153 33..34 33 - - - Clinvar_Rec_419 81844 RMVar_ID_81844 Human_SNP_ID_658502158 m1A Human chr19 + 11449286 11449282 11449286 GCCCATCCCCAGGTGCGCCTCCTGTGCGGGAAAGAGACCATGGTGACCAGCACCACAGAGCCCAG GCCCATCCCCAGGTGCGCCTCCTGTGCGG____GAGACCATGGTGACCAGCACCACAGAGCCCAG GGAAA G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11448526..11449500 32194978 MeRIP-seq:(Medium) rs794727187 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_913830,Human_RBP_ID_8476847,Human_RBP_ID_13365985,Human_RBP_ID_18191984,Human_RBP_ID_22447430,Human_RBP_ID_22762784 Human_Splice_Rec_1960690,Human_Splice_Rec_1960774,Human_Splice_Rec_1960816,Human_Splice_Rec_1960848,Human_Splice_Rec_1960878,Human_Splice_Rec_1960886,Human_Splice_Rec_1960894 RMVar_hsa_circ_112721,RMVar_hsa_circ_41607,RMVar_hsa_circ_370034,RMVar_hsa_circ_192599,RMVar_hsa_circ_192600 81845 RMVar_ID_81845 Human_SNP_ID_658502159 m1A Human chr19 + 11449286 11449286 11449286 GCCCATCCCCAGGTGCGCCTCCTGTGCGGGAAAGAGACCATGGTGACCAGCACCACAGAGCCCAG GCCCATCCCCAGGTGCGCCTCCTGTGCGGGAAGGAGACCATGGTGACCAGCACCACAGAGCCCAG A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11448526..11449500 32194978 MeRIP-seq:(Medium) rs369863173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913830,Human_RBP_ID_8476847,Human_RBP_ID_13365985,Human_RBP_ID_18191984,Human_RBP_ID_22447430,Human_RBP_ID_22762784 Human_Splice_Rec_1960690,Human_Splice_Rec_1960774,Human_Splice_Rec_1960816,Human_Splice_Rec_1960848,Human_Splice_Rec_1960878,Human_Splice_Rec_1960886,Human_Splice_Rec_1960894 RMVar_hsa_circ_112721,RMVar_hsa_circ_41607,RMVar_hsa_circ_370034,RMVar_hsa_circ_192599,RMVar_hsa_circ_192600 81846 RMVar_ID_81846 Human_SNP_ID_658502217 m1A Human chr19 - 11449430 11449430 11449430 GGGCAGGCCGACGAGACTCCACCTCCCCGCCCACCTCTGCGCCCATCCAGCTAGAGCTCGTCATG GGGCAGGCCGACGAGACTCCACCTCCCCGCCCGCCTCTGCGCCCATCCAGCTAGAGCTCGTCATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11449419..11449507 26863196 MeRIP-seq:(Medium) rs756919797 Functional Loss SNV dbSNP153 33..33 33 - - - 81847 RMVar_ID_81847 Human_SNP_ID_658502218 m1A Human chr19 - 11449430 11449430 11449430 GGGCAGGCCGACGAGACTCCACCTCCCCGCCCACCTCTGCGCCCATCCAGCTAGAGCTCGTCATG GGGCAGGCCGACGAGACTCCACCTCCCCGCCCCCCTCTGCGCCCATCCAGCTAGAGCTCGTCATG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11449419..11449507 26863196 MeRIP-seq:(Medium) rs756919797 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 81848 RMVar_ID_81848 Human_SNP_ID_658502372 m1A Human chr19 + 11449900 11449899 11449900 ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCAATGGCGCGATCTCGGCTCACTGCAACCTCCAC ACTCTTGTTGCCGAGGCTGGAATGTGGAATGC_ATGGCGCGATCTCGGCTCACTGCAACCTCCAC CA C PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1228567440 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13366005,Human_RBP_ID_26464346 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 81849 RMVar_ID_81849 Human_SNP_ID_658502374 m1A Human chr19 + 11449900 11449900 11449900 ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCAATGGCGCGATCTCGGCTCACTGCAACCTCCAC ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCGATGGCGCGATCTCGGCTCACTGCAACCTCCAC A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs924938160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13366005,Human_RBP_ID_26464346 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 81850 RMVar_ID_81850 Human_SNP_ID_658507499 m1A Human chr19 + 11465208 11465205 11465209 ACATACACGTAATACACCTACACGCCACACACATACACACACACCACACACATACACACCGCACA ACATACACGTAATACACCTACACGCCACAC____ACACACACACCACACACATACACACCGCACA CACAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11464956..11465286 26863196 MeRIP-seq:(Medium) rs1007232599 Functional Loss DEL dbSNP153 31..34 33 - - - 81851 RMVar_ID_81851 Human_SNP_ID_658512819 m1A Human chr19 - 11483577 11483577 11483577 CAGCTGCGAGGGCCGCCCGGACCGCGGGCCGGAAGGAGGCGCCCCCGCCCCGCCCCAGAGCTGGG CAGCTGCGAGGGCCGCCCGGACCGCGGGCCGGGAGGAGGCGCCCCCGCCCCGCCCCAGAGCTGGG T C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:11483475..11483814;chr19:11483544..11483652 26863196 MeRIP-seq:(Medium) rs1444672916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108017,RMVar_hsa_circ_192608 81852 RMVar_ID_81852 Human_SNP_ID_658514100 m1A Human chr19 + 11487146 11487146 11487146 GCTCCTCCTTCTCCTCCTTCTTTAGCAAGCACAGGTCCTCCTTCTCTACAGGGTGGACACAGGGT GCTCCTCCTTCTCCTCCTTCTTTAGCAAGCACGGGTCCTCCTTCTCTACAGGGTGGACACAGGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:11485732..11487634 26863196 MeRIP-seq:(Medium) rs769434482 Functional Loss SNV dbSNP153 33..33 33 - - - 81853 RMVar_ID_81853 Human_SNP_ID_658514191 m1A Human chr19 - 11487363 11487363 11487363 TGCCATGATGGAGGGTGTGGCAGCCTACACCCAGACAGAGCCCGAGGGTAGCCAGCCTAGCACCA TGCCATGATGGAGGGTGTGGCAGCCTACACCCGGACAGAGCCCGAGGGTAGCCAGCCTAGCACCA T C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11487290..11487430 26863196 MeRIP-seq:(Medium) rs1314632612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1960945,Human_Splice_Rec_1960973 RMVar_hsa_circ_329215,RMVar_hsa_circ_128196,RMVar_hsa_circ_192610,RMVar_hsa_circ_23942 81854 RMVar_ID_81854 Human_SNP_ID_658514213 m1A Human chr19 - 11487421 11487420 11487421 TCAACATGGCAGCAGGCAGCGGTGTCCCCGGCAGTGGACTGGGCGAGGAGGTGCCCTGTGCCATG TCAACATGGCAGCAGGCAGCGGTGTCCCCGGC_GTGGACTGGGCGAGGAGGTGCCCTGTGCCATG CT C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11487280..11487428 32194978 MeRIP-seq:(Medium) rs1303407088 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_54346 RMVar_hsa_circ_329215,RMVar_hsa_circ_128196,RMVar_hsa_circ_192610,RMVar_hsa_circ_23942 81855 RMVar_ID_81855 Human_SNP_ID_658514385 m1A Human chr19 + 11487771 11487771 11487771 CGCCCTCCTGAGTGATGAGCCCGCTGCTGCCCACCGGGCTGGTGGGCGTCGCTGCCGCTGCCGCT CGCCCTCCTGAGTGATGAGCCCGCTGCTGCCCGCCGGGCTGGTGGGCGTCGCTGCCGCTGCCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr19:11487736..11487861;chr19:11487723..11487872 26863196,32194978 MeRIP-seq:(Medium) rs1052372556 Functional Loss SNV dbSNP153 33..33 33 - - - 81856 RMVar_ID_81856 Human_SNP_ID_658517760 m1A Human chr19 - 11500046 11500045 11500046 CAAGAGCAGGTCTGGGCCACAGCAGGGAGGCCAGGGGGCCCAGGCTCCACGATGATACTGATAAT CAAGAGCAGGTCTGGGCCACAGCAGGGAGGCC_GGGGGCCCAGGCTCCACGATGATACTGATAAT CT C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11500037..11500371 26863196 MeRIP-seq:(Medium) rs1451704093 Functional Loss DEL dbSNP153 33..33 33 - - - 81857 RMVar_ID_81857 Human_SNP_ID_658517772 m1A Human chr19 - 11500106 11500106 11500106 AGACGGGGTGGACAGTTTTGCTGATAAGAGACACTAGACTGGCTGTCAGGATGTTTGTGGCAAGA AGACGGGGTGGACAGTTTTGCTGATAAGAGACGCTAGACTGGCTGTCAGGATGTTTGTGGCAAGA T C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11500104..11500289 26863196 MeRIP-seq:(Medium) rs1568397245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13366114 81858 RMVar_ID_81858 Human_SNP_ID_658519353 m1A Human chr19 - 11505703 11505703 11505703 GCGGGCGGGGAGGCAGCAGCCGAGGAGGGCGCAGCGGGCCGAAAGGCGCGGGGCCGGCCGCGACT GCGGGCGGGGAGGCAGCAGCCGAGGAGGGCGCCGCGGGCCGAAAGGCGCGGGGCCGGCCGCGACT T G ZNF653 Ensembl:ENSG00000161914 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:11505614..11505777 26863196 MeRIP-seq:(Medium) rs1411736799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8218,Human_RBP_ID_241759,Human_RBP_ID_5373228,Human_RBP_ID_9328642,Human_RBP_ID_9428098,Human_RBP_ID_18994381,Human_RBP_ID_27816116 81859 RMVar_ID_81859 Human_SNP_ID_658519411 m1A Human chr19 + 11505770 11505770 11505770 CCGCCTCAGCCTCCGCCTCCGCCTCGGGCTCTAGCGCCCGCTCCGCCATCCCCCCCACCCTGGTT CCGCCTCAGCCTCCGCCTCCGCCTCGGGCTCTGGCGCCCGCTCCGCCATCCCCCCCACCCTGGTT A G NONHSAG024846.2 RNACentral:URS00009B9550 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:11505700..11505784 26863410 MeRIP-seq:(Medium) rs1384306877 Functional Loss SNV dbSNP153 33..33 33 - - - 81860 RMVar_ID_81860 Human_SNP_ID_658519716 m1A Human chr19 - 11506323 11506323 11506323 GGGCCTGCAGGAGACCAACCCAACCCTGGCCCAGATCCCCGTGGTCTTCCGCCTCGCCGGGTCCA GGGCCTGCAGGAGACCAACCCAACCCTGGCCCGGATCCCCGTGGTCTTCCGCCTCGCCGGGTCCA T C ECSIT Ensembl:ENSG00000130159 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:11506276..11506375 32194978 MeRIP-seq:(Medium) rs779687690 Functional Loss SNV dbSNP153 33..33 33 - - - 81861 RMVar_ID_81861 Human_SNP_ID_658520092 m1A Human chr19 - 11507516 11507516 11507516 GCCGGAGGAGTGGAACCTCTACTACCCGATGCAGCTGGACCTGGAGTATGTGAGGAGTGGCTGGG GCCGGAGGAGTGGAACCTCTACTACCCGATGCTGCTGGACCTGGAGTATGTGAGGAGTGGCTGGG T A ECSIT Ensembl:ENSG00000130159 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11507439..11507589 26863196 MeRIP-seq:(Medium) rs1161330474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512934,Human_RBP_ID_6718763,Human_RBP_ID_17694535 Human_Splice_Rec_1960996,Human_Splice_Rec_1960997,Human_Splice_Rec_1961010,Human_Splice_Rec_1961011,Human_Splice_Rec_1961022,Human_Splice_Rec_1961023,Human_Splice_Rec_1961032,Human_Splice_Rec_1961033,Human_Splice_Rec_1961042,Human_Splice_Rec_1961043,Human_Splice_Rec_1961045,Human_Splice_Rec_1961058,Human_Splice_Rec_1961059,Human_Splice_Rec_1961068,Human_Splice_Rec_1961069,Human_Splice_Rec_1961080 RMVar_hsa_circ_192612,RMVar_hsa_circ_272282,RMVar_hsa_circ_343331,RMVar_hsa_circ_324078,RMVar_hsa_circ_192613 81862 RMVar_ID_81862 Human_SNP_ID_658520100 m1A Human chr19 + 11507526 11507526 11507526 CCTCACATACTCCAGGTCCAGCTGCATCGGGTAGTAGAGGTTCCACTCCTCCGGCGTCTCTTCCA CCTCACATACTCCAGGTCCAGCTGCATCGGGTCGTAGAGGTTCCACTCCTCCGGCGTCTCTTCCA A C NONHSAG024846.2 RNACentral:URS00009B9550 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11507476..11507550 32194978 MeRIP-seq:(Medium) rs781302551 Functional Loss SNV dbSNP153 33..33 33 - - - 81863 RMVar_ID_81863 Human_SNP_ID_658525688 m1A Human chr19 + 11529094 11529094 11529094 CTACTCACGCGGCCAGCCGCGGACTCCAGGCCAGCTCTGTCTTGTTGCTGGGCGCTGCCATATTG CTACTCACGCGGCCAGCCGCGGACTCCAGGCCTGCTCTGTCTTGTTGCTGGGCGCTGCCATATTG A T lnc-CNN1-2 RNACentral:URS00008C3BC4 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11529009..11529095 26863196 MeRIP-seq:(Medium) rs1422330863 Functional Loss SNV dbSNP153 33..33 33 - - - 81864 RMVar_ID_81864 Human_SNP_ID_658529047 m1A Human chr19 - 11541192 11541192 11541192 GGTCTCGGCTTCGAGAGCCTCACTCACTCGCAAAGAATGATGCCATCTTTGAGGCCGTCCATGAA GGTCTCGGCTTCGAGAGCCTCACTCACTCGCAGAGAATGATGCCATCTTTGAGGCCGTCCATGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:11541141..11541966 32194978 MeRIP-seq:(Medium) rs1201948338 Functional Loss SNV dbSNP153 33..33 33 - - - 81865 RMVar_ID_81865 Human_SNP_ID_658531697 m1A Human chr19 - 11550023 11550023 11550023 TTGCTCAGTGCGTCCTTTGGGCGCTGTTGGGGACACCCGGCTCTATGTTGGACCCTGTAGCACTA TTGCTCAGTGCGTCCTTTGGGCGCTGTTGGGGCCACCCGGCTCTATGTTGGACCCTGTAGCACTA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:11549974..11550273;chr19:11549974..11550074 32194978 MeRIP-seq:(Medium) rs552220753 Functional Loss SNV dbSNP153 33..33 33 - - - 81866 RMVar_ID_81866 Human_SNP_ID_658532940 m1A Human chr19 + 11553631 11553631 11553631 ACACACACACACACACACACACACACACACACACGGCTGTGACAGCCCAGGACCCACACCCTGGA ACACACACACACACACACACACACACACACACGCGGCTGTGACAGCCCAGGACCCACACCCTGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:11553580..11553680 32194978 MeRIP-seq:(Medium) rs1450600949 Functional Loss SNV dbSNP153 33..33 33 - - - 81867 RMVar_ID_81867 Human_SNP_ID_658533212 m1A Human chr19 + 11554346 11554346 11554346 GAGGCGGCTTTCGTTTTGACTTTCTGCGCCCCATGTCTGCAGGTGGATGAGCCTGTGGGGAGTGG GAGGCGGCTTTCGTTTTGACTTTCTGCGCCCCGTGTCTGCAGGTGGATGAGCCTGTGGGGAGTGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:11554151..11554402 26863196 MeRIP-seq:(Medium) rs1195625825 Functional Loss SNV dbSNP153 33..33 33 - - - 81868 RMVar_ID_81868 Human_SNP_ID_658533218 m1A Human chr19 + 11554360 11554360 11554360 TTTGACTTTCTGCGCCCCATGTCTGCAGGTGGATGAGCCTGTGGGGAGTGGCAGATGTCAGTGGT TTTGACTTTCTGCGCCCCATGTCTGCAGGTGGCTGAGCCTGTGGGGAGTGGCAGATGTCAGTGGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:11554001..11554599 26863196 MeRIP-seq:(Medium) rs762056453 Functional Loss SNV dbSNP153 33..33 33 - - - 81869 RMVar_ID_81869 Human_SNP_ID_658534367 m1A Human chr19 - 11559128 11559124 11559129 CGTTGGGGGTGGGCAGGACTGGAAGTTCCTCTACTCCGTGCGTTTACGGGGTCCTGGAGGAGGCT CGTTGGGGGTGGGCAGGACTGGAAGTTCCTC_____CGTGCGTTTACGGGGTCCTGGAGGAGGCT GGAGTA G ELOF1 Ensembl:ENSG00000130165 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11559125..11559225 26863196 MeRIP-seq:(Medium) rs1450385072 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_826441,Human_RBP_ID_910686,Human_RBP_ID_5370008,Human_RBP_ID_20353585,Human_RBP_ID_26784013 RMVar_hsa_circ_108045,RMVar_hsa_circ_192624,RMVar_hsa_circ_192625,RMVar_hsa_circ_98555 81870 RMVar_ID_81870 Human_SNP_ID_658562809 m1A Human chr19 - 11666987 11666987 11666987 AGAGTCTCCTAAAGAGCCCGAACAGCTGAGGAAGCTCTTCATTGGAGGGTTGAGCTTTGAAACAA AGAGTCTCCTAAAGAGCCCGAACAGCTGAGGAGGCTCTTCATTGGAGGGTTGAGCTTTGAAACAA T C HNRNPA1P10 Ensembl:ENSG00000214223 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1249219805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1903100 81871 RMVar_ID_81871 Human_SNP_ID_658653218 m1A Human chr19 - 12018287 12018287 12018287 CTCCTCTATACATGTGAGATGTTTCAGGATTCAGTGGCCTTTGAGGATGTGGCTGTGACCTTCAC CTCCTCTATACATGTGAGATGTTTCAGGATTCCGTGGCCTTTGAGGATGTGGCTGTGACCTTCAC T G ZNF433,AC008770.1 Ensembl:ENSG00000197647,Ensembl:ENSG00000257355 Protein coding,Protein coding 5'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12018236..12018340 32194978 MeRIP-seq:(Medium) rs768537111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4501362 Human_Splice_Rec_1961604,Human_Splice_Rec_1961610,Human_Splice_Rec_1961616,Human_Splice_Rec_1961624,Human_Splice_Rec_1961638,Human_Splice_Rec_1961650,Human_Splice_Rec_1961658,Human_Splice_Rec_1961666,Human_Splice_Rec_1961672 RMVar_hsa_circ_40392,RMVar_hsa_circ_350862 81872 RMVar_ID_81872 Human_SNP_ID_658691999 m1A Human chr19 - 12163135 12163134 12163136 GATCCCAAGGCAGGTACAGGAAACCGCGCCACAGAGACTCCAGGCGAGCCACTCTGGGCCTCTGG GATCCCAAGGCAGGTACAGGAAACCGCGCCA__GAGACTCCAGGCGAGCCACTCTGGGCCTCTGG CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12163085..12163191 26863196 MeRIP-seq:(Medium) rs1362525642 Functional Loss DEL dbSNP153 32..33 33 - - - 81873 RMVar_ID_81873 Human_SNP_ID_658700455 m1A Human chr19 + 12194947 12194947 12194947 TGTGAAGAGGGCGGGGCTTCGTGAACTGTCCAATCAGAGGCGCCACGTGGAAGGTGGGTGGGGCA TGTGAAGAGGGCGGGGCTTCGTGAACTGTCCAGTCAGAGGCGCCACGTGGAAGGTGGGTGGGGCA A G LOC100289333,LOC100289333:2 RNACentral:URS00008B3D03,RNACentral:URS00008BDF02 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12194897..12195042 26863196 MeRIP-seq:(Medium) rs1487749341 Functional Loss SNV dbSNP153 33..33 33 - - - 81874 RMVar_ID_81874 Human_SNP_ID_658716256 m1A Human chr19 - 12260165 12260165 12260165 AGGTCGGCATAGTCCTCTTGATCAGAAACTGGAGCAGTTCTGCACGACCATCCATTGCAGATGCG AGGTCGGCATAGTCCTCTTGATCAGAAACTGGGGCAGTTCTGCACGACCATCCATTGCAGATGCG T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12260118..12260201 26863196 MeRIP-seq:(Medium) rs1011011752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76204,RMVar_hsa_circ_122888,RMVar_hsa_circ_192664,RMVar_hsa_circ_192666,RMVar_hsa_circ_21851,RMVar_hsa_circ_192669,RMVar_hsa_circ_192671,RMVar_hsa_circ_359855,RMVar_hsa_circ_192673 81875 RMVar_ID_81875 Human_SNP_ID_658719146 m1A Human chr19 + 12271971 12271971 12271971 TACTGGAACCAATCTTCTTGCATATAGCAGGCAGCAACTCTATTTGAAAGAAATGGAAACTTTTT TACTGGAACCAATCTTCTTGCATATAGCAGGCGGCAACTCTATTTGAAAGAAATGGAAACTTTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12271956..12272036 32194978 MeRIP-seq:(Medium) rs1444914934 Functional Loss SNV dbSNP153 33..33 33 - - - 81876 RMVar_ID_81876 Human_SNP_ID_658808730 m1A Human chr19 + 12610982 12610982 12610982 TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGACGCGTCAGGTTGCTGTACCCCTGCATCGGATG TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGCCGCGTCAGGTTGCTGTACCCCTGCATCGGATG A C ZNF791 Ensembl:ENSG00000173875 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12610926..12611101 26863196 MeRIP-seq:(Medium) rs927983312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554370,Human_RBP_ID_4558105,Human_RBP_ID_8477102,Human_RBP_ID_13369547,Human_RBP_ID_18420861,Human_RBP_ID_26335767 81877 RMVar_ID_81877 Human_SNP_ID_658808731 m1A Human chr19 + 12610982 12610982 12610982 TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGACGCGTCAGGTTGCTGTACCCCTGCATCGGATG TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGGCGCGTCAGGTTGCTGTACCCCTGCATCGGATG A G ZNF791 Ensembl:ENSG00000173875 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12610926..12611101 26863196 MeRIP-seq:(Medium) rs927983312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554370,Human_RBP_ID_4558105,Human_RBP_ID_8477102,Human_RBP_ID_13369547,Human_RBP_ID_18420861,Human_RBP_ID_26335767 81878 RMVar_ID_81878 Human_SNP_ID_658808732 m1A Human chr19 + 12610982 12610982 12610982 TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGACGCGTCAGGTTGCTGTACCCCTGCATCGGATG TTGTGCTTAGCTTGGGGTCTCCTGGCCCCTTGTCGCGTCAGGTTGCTGTACCCCTGCATCGGATG A T ZNF791 Ensembl:ENSG00000173875 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12610926..12611101 26863196 MeRIP-seq:(Medium) rs927983312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554370,Human_RBP_ID_4558105,Human_RBP_ID_8477102,Human_RBP_ID_13369547,Human_RBP_ID_18420861,Human_RBP_ID_26335767 81879 RMVar_ID_81879 Human_SNP_ID_658808739 m1A Human chr19 + 12611007 12611006 12611007 CCCCTTGACGCGTCAGGTTGCTGTACCCCTGCATCGGATGCGCTGTACCCTGCGCTGGCTCCGTG CCCCTTGACGCGTCAGGTTGCTGTACCCCTGC_TCGGATGCGCTGTACCCTGCGCTGGCTCCGTG CA C ZNF791 Ensembl:ENSG00000173875 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12610958..12611069 26863196 MeRIP-seq:(Medium) rs1226068864 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4501927,Human_RBP_ID_13369547,Human_RBP_ID_18420861,Human_RBP_ID_26335767 Human_Splice_Rec_1962161,Human_Splice_Rec_1962165,Human_Splice_Rec_1962173,Human_Splice_Rec_1962179,Human_Splice_Rec_1962185,Human_Splice_Rec_1962189 81880 RMVar_ID_81880 Human_SNP_ID_658818417 m1A Human chr19 + 12643932 12643932 12643932 CGGGCGGGGCGGCGGCCCATGGCGACACCAGGATCTTCAGTGGCACACTGAAGGGAAAGAGAAAT CGGGCGGGGCGGCGGCCCATGGCGACACCAGGTTCTTCAGTGGCACACTGAAGGGAAAGAGAAAT A T RF00017-1304,lnc-ZNF791-3 RNACentral:URS0000990DE9,RNACentral:URS00008C06C9 SRP RNA,lincRNA intron,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:12643847..12643933 26863410 MeRIP-seq:(Medium) rs1262371214 Functional Loss SNV dbSNP153 33..33 33 - - - 81881 RMVar_ID_81881 Human_SNP_ID_658819791 m1A Human chr19 + 12648363 12648363 12648363 CGCCCCCGACCCGTTCTCCATTAGTGGCTCCGATACTCCGCGTCCATCGTCCTTCAGCAGCCTTC CGCCCCCGACCCGTTCTCCATTAGTGGCTCCGGTACTCCGCGTCCATCGTCCTTCAGCAGCCTTC A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:12648283..12648428;chr19:12648259..12648443 26863196 MeRIP-seq:(Medium) rs1568297991 Functional Loss SNV dbSNP153 33..33 33 - - - 81882 RMVar_ID_81882 Human_SNP_ID_658825155 m1A Human chr19 + 12665474 12665474 12665474 AGCGACGGGTGGGATCTGCCAGCAAGGCAGAGATGACCGAGTCCAGGATGTACTGCACACCGGCG AGCGACGGGTGGGATCTGCCAGCAAGGCAGAGCTGACCGAGTCCAGGATGTACTGCACACCGGCG A C RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:12665351..12665712 26863196 MeRIP-seq:(Medium) rs1347890014 Functional Loss SNV dbSNP153 33..33 33 - - - 81883 RMVar_ID_81883 Human_SNP_ID_658825277 m1A Human chr19 - 12665803 12665803 12665803 AAGGTATGTGTGTTTGGGGTCCCTGTGCAGACATGCCCCACAGTGCAGCCGAACATGCTGAACGT AAGGTATGTGTGTTTGGGGTCCCTGTGCAGACGTGCCCCACAGTGCAGCCGAACATGCTGAACGT T C MAN2B1,AC010422.5 Ensembl:ENSG00000104774,Ensembl:ENSG00000269590 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12665701..12665825 26863196 MeRIP-seq:(Medium) rs1441130613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770464,Human_RBP_ID_4502208 Human_Splice_Rec_1962202,Human_Splice_Rec_1962254,Human_Splice_Rec_1962300,Human_Splice_Rec_1962400,Human_Splice_Rec_1962406,Human_Splice_Rec_1962412 RMVar_hsa_circ_95806,RMVar_hsa_circ_192704 81884 RMVar_ID_81884 Human_SNP_ID_658825562 m1A Human chr19 + 12666700 12666699 12666701 CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCCATGGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCC__GGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG CAT C RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr19:12666651..12666725;chr19:12666601..12666725 26863196,26863410 MeRIP-seq:(Medium) rs1290585382 Functional Loss DEL dbSNP153 33..34 33 - - - Clinvar_Rec_420 81885 RMVar_ID_81885 Human_SNP_ID_658825563 m1A Human chr19 + 12666700 12666700 12666700 CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCCATGGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCCGTGGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr19:12666651..12666725;chr19:12666601..12666725 26863196,26863410 MeRIP-seq:(Medium) rs1555710357 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_421,Clinvar_Rec_422 81886 RMVar_ID_81886 Human_SNP_ID_658825564 m1A Human chr19 + 12666700 12666700 12666700 CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCCATGGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG CGCAGACCCCCGAAGCCCGCGCGTAGGCGCCCTTGGCTCAGCAGCTTCCTCCTGGGGTTCCCCGG A T RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr19:12666651..12666725;chr19:12666601..12666725 26863196,26863410 MeRIP-seq:(Medium) rs1555710357 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_421,Clinvar_Rec_422 81887 RMVar_ID_81887 Human_SNP_ID_658826827 m1A Human chr19 + 12670246 12670246 12670246 GGGGACAAGGCGGTGGTTCTGTGGGATGTGGCATCAGGGCAGGTCGTGCGCAAATTCCGGGGCCA GGGGACAAGGCGGTGGTTCTGTGGGATGTGGCGTCAGGGCAGGTCGTGCGCAAATTCCGGGGCCA A G WDR83 Ensembl:ENSG00000123154 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12669829..12670256 32194978 MeRIP-seq:(Medium) rs769505285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1962422,Human_Splice_Rec_1962423,Human_Splice_Rec_1962442,Human_Splice_Rec_1962443,Human_Splice_Rec_1962462,Human_Splice_Rec_1962463,Human_Splice_Rec_1962482,Human_Splice_Rec_1962483,Human_Splice_Rec_1962494,Human_Splice_Rec_1962495,Human_Splice_Rec_1962504,Human_Splice_Rec_1962505,Human_Splice_Rec_1962516,Human_Splice_Rec_1962517,Human_Splice_Rec_1962522,Human_Splice_Rec_1962523,Human_Splice_Rec_1962530,Human_Splice_Rec_1962531,Human_Splice_Rec_1962539 RMVar_hsa_circ_192717,RMVar_hsa_circ_86222 81888 RMVar_ID_81888 Human_SNP_ID_658831140 m1A Human chr19 - 12681737 12681726 12681738 CGCATGGAAGGTTCCCTGGAACGGGAGGCGCCAGCGGGGGCGCTGGCCGCCGTGCTAAAGCACAG CGCATGGAAGGTTCCCTGGAACGGGAGGCGC____________TGGCCGCCGTGCTAAAGCACAG AGCGCCCCCGCTG A DHPS,AC010422.8 Ensembl:ENSG00000095059,Ensembl:ENSG00000285589 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12681649..12681825 26863196 MeRIP-seq:(Medium) rs1324953393 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_241163,Human_RBP_ID_9328646 81889 RMVar_ID_81889 Human_SNP_ID_658831175 m1A Human chr19 + 12681775 12681775 12681775 CTCCCGTTCCAGGGAACCTTCCATGCGCCTATAGCCGGCTCTCGAGTCAAAGCTGCCCCTAGGCC CTCCCGTTCCAGGGAACCTTCCATGCGCCTATTGCCGGCTCTCGAGTCAAAGCTGCCCCTAGGCC A T RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12681730..12681817 26863196 MeRIP-seq:(Medium) rs202182413 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 81890 RMVar_ID_81890 Human_SNP_ID_658831188 m1A Human chr19 + 12681793 12681793 12681793 TTCCATGCGCCTATAGCCGGCTCTCGAGTCAAAGCTGCCCCTAGGCCGGGCTTACGGCGGCCCAG TTCCATGCGCCTATAGCCGGCTCTCGAGTCAATGCTGCCCCTAGGCCGGGCTTACGGCGGCCCAG A T RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12681744..12681825 26863196 MeRIP-seq:(Medium) rs1395493751 Functional Loss SNV dbSNP153 33..33 33 - - - 81891 RMVar_ID_81891 Human_SNP_ID_658832806 m1A Human chr19 - 12686192 12686192 12686192 CAAAAAAGAGCTTGGTGGGTTCCAGGAATAGCAAAGAGGTCTGTGTAGCTGGAGAGGAGAGAGGG CAAAAAAGAGCTTGGTGGGTTCCAGGAATAGCGAAGAGGTCTGTGTAGCTGGAGAGGAGAGAGGG T C AC010422.2 Ensembl:ENSG00000268945 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12686053..12686351 26863196 MeRIP-seq:(Medium) rs1184656010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5193973,Human_RBP_ID_5248676 81892 RMVar_ID_81892 Human_SNP_ID_658832828 m1A Human chr19 - 12686292 12686291 12686292 TCAGAGGAGGTGACATTTGAACTTAGGCCCAAAGGAGGAGAAGGAACTGAGAAATGGGGTGTTCT TCAGAGGAGGTGACATTTGAACTTAGGCCCAA_GGAGGAGAAGGAACTGAGAAATGGGGTGTTCT CT C AC010422.2 Ensembl:ENSG00000268945 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12686183..12686374 26863196 MeRIP-seq:(Medium) rs146351180 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13370536 81893 RMVar_ID_81893 Human_SNP_ID_658837103 m1A Human chr19 - 12699464 12699459 12699465 TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTAAAAAAAAACTATTTAATTTTTTAATTTATTTT TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTT______AAAACTATTTAATTTTTTAATTTATTTT TTTTTTA T TNPO2 Ensembl:ENSG00000105576 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1168553188 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_6720738,Human_RBP_ID_22966817 81894 RMVar_ID_81894 Human_SNP_ID_658837109 m1A Human chr19 - 12699464 12699460 12699465 TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTAAAAAAAAACTATTTAATTTTTTAATTTATTTT TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTT_____AAAAACTATTTAATTTTTTAATTTATTTT TTTTTA T TNPO2 Ensembl:ENSG00000105576 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1355334041 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_6720738,Human_RBP_ID_22966817 81895 RMVar_ID_81895 Human_SNP_ID_658837113 m1A Human chr19 - 12699464 12699461 12699465 TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTAAAAAAAAACTATTTAATTTTTTAATTTATTTT TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTT____AAAAAACTATTTAATTTTTTAATTTATTTT TTTTA T TNPO2 Ensembl:ENSG00000105576 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1391052794 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_6720738,Human_RBP_ID_22966817 81896 RMVar_ID_81896 Human_SNP_ID_658837121 m1A Human chr19 - 12699464 12699464 12699464 TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTAAAAAAAAACTATTTAATTTTTTAATTTATTTT TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTTAAAAAAAACTATTTAATTTTTTAATTTATTTT T A TNPO2 Ensembl:ENSG00000105576 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs868115219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6720738,Human_RBP_ID_22966817 81897 RMVar_ID_81897 Human_SNP_ID_658837251 m1A Human chr19 + 12699984 12699963 12699984 TCTGCAAGGCCCAGTTTTCTGGCCAACTGGGAAGTAACTACACCCCCACCCTCTCTAGGGGAGCC TCTGCAAGGCCC_____________________GTAACTACACCCCCACCCTCTCTAGGGGAGCC CAGTTTTCTGGCCAACTGGGAA C RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12699741..12700091 32194978 MeRIP-seq:(Medium) rs1416807246 Functional Loss DEL dbSNP153 13..33 33 - - - 81898 RMVar_ID_81898 Human_SNP_ID_658838981 m1A Human chr19 - 12705601 12705601 12705601 CTGAGTTCTCCCCACCTGCCTTCCTCCCTGCCAGTGTCTGTCATCGGTGGCCACCGCCCTGCAGA CTGAGTTCTCCCCACCTGCCTTCCTCCCTGCCGGTGTCTGTCATCGGTGGCCACCGCCCTGCAGA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12705588..12705664 26863196 MeRIP-seq:(Medium) rs1277750042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513413,Human_RBP_ID_3954531,Human_RBP_ID_19089358,Human_RBP_ID_22966837,Human_RBP_ID_25441278,Human_RBP_ID_26982899 RMVar_hsa_circ_105206,RMVar_hsa_circ_94848,RMVar_hsa_circ_89937,RMVar_hsa_circ_126336,RMVar_hsa_circ_18945,RMVar_hsa_circ_27703,RMVar_hsa_circ_192731,RMVar_hsa_circ_192730,RMVar_hsa_circ_120313,RMVar_hsa_circ_192733,RMVar_hsa_circ_192734,RMVar_hsa_circ_118706,RMVar_hsa_circ_99856,RMVar_hsa_circ_192736,RMVar_hsa_circ_102698,RMVar_hsa_circ_192737,RMVar_hsa_circ_192738,RMVar_hsa_circ_112083,RMVar_hsa_circ_192740,RMVar_hsa_circ_111022,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,RMVar_hsa_circ_192741,RMVar_hsa_circ_192742,RMVar_hsa_circ_100778,RMVar_hsa_circ_332171,RMVar_hsa_circ_370073,RMVar_hsa_circ_192743,RMVar_hsa_circ_373724,RMVar_hsa_circ_341201,RMVar_hsa_circ_98766,RMVar_hsa_circ_287917,RMVar_hsa_circ_44442,RMVar_hsa_circ_192746,RMVar_hsa_circ_192748,RMVar_hsa_circ_192749,RMVar_hsa_circ_192747 81899 RMVar_ID_81899 Human_SNP_ID_658843890 m1A Human chr19 + 12722550 12722549 12722551 CTCCAGAGACTCGCGCGGAAGGAGGGAGCCAAAGAGAGAGAATTAAAAAAAAAAAAAAAAAAAAA CTCCAGAGACTCGCGCGGAAGGAGGGAGCCAA__AGAGAGAATTAAAAAAAAAAAAAAAAAAAAA AAG A RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12722548..12722641 26863196 MeRIP-seq:(Medium) rs1237463468 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22391068 81900 RMVar_ID_81900 Human_SNP_ID_658844301 m1A Human chr19 + 12723905 12723905 12723905 ATCGCGGAAGACACCCTAAAGGAGCAGTTGGGATTCCGAGGTAGCCAGTTCCGCTGGACTGAAAC ATCGCGGAAGACACCCTAAAGGAGCAGTTGGGGTTCCGAGGTAGCCAGTTCCGCTGGACTGAAAC A G RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12723854..12723959 26863196 MeRIP-seq:(Medium) rs1296526916 Functional Loss SNV dbSNP153 33..33 33 - - - 81901 RMVar_ID_81901 Human_SNP_ID_658846388 m1A Human chr19 + 12730924 12730923 12730925 CTGCCGCTGCATTAAATAGTTATGTACATCGCAGAGAGTCCCAGGCCATGGGCAGGTGGGGGAGG CTGCCGCTGCATTAAATAGTTATGTACATCGC__AGAGTCCCAGGCCATGGGCAGGTGGGGGAGG CAG C RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12730726..12731545 32194978 MeRIP-seq:(Medium) rs758810543 Functional Loss DEL dbSNP153 33..34 33 - - - 81902 RMVar_ID_81902 Human_SNP_ID_658846389 m1A Human chr19 + 12730924 12730924 12730924 CTGCCGCTGCATTAAATAGTTATGTACATCGCAGAGAGTCCCAGGCCATGGGCAGGTGGGGGAGG CTGCCGCTGCATTAAATAGTTATGTACATCGCGGAGAGTCCCAGGCCATGGGCAGGTGGGGGAGG A G RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12730726..12731545 32194978 MeRIP-seq:(Medium) rs753946306 Functional Loss SNV dbSNP153 33..33 33 - - - 81903 RMVar_ID_81903 Human_SNP_ID_658846502 m1A Human chr19 + 12731329 12731329 12731329 GAAGGGAAAGGCAATGTGGGTGGACCCCCTGCACCAAGCTGGCTCACCTCATCCTCCGTCTTCTG GAAGGGAAAGGCAATGTGGGTGGACCCCCTGCCCCAAGCTGGCTCACCTCATCCTCCGTCTTCTG A C RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12731326..12731562 26863196 MeRIP-seq:(Medium) rs1198134055 Functional Loss SNV dbSNP153 33..33 33 - - - 81904 RMVar_ID_81904 Human_SNP_ID_658847340 m1A Human chr19 + 12734364 12734364 12734364 GGACCGCCCTTCCTCTTCGGATCCCCGGGGCCAGCGGCGGCGGCCGACTGGTCGGGTCGCTGCGG GGACCGCCCTTCCTCTTCGGATCCCCGGGGCCGGCGGCGGCGGCCGACTGGTCGGGTCGCTGCGG A G RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12734301..12734650 32194978 MeRIP-seq:(Medium) rs1201211736 Functional Loss SNV dbSNP153 33..33 33 - - - 81905 RMVar_ID_81905 Human_SNP_ID_658847412 m1A Human chr19 - 12734569 12734569 12734569 GGGCGGTGGCGGTGGCGGGAGCCGTTGGGCTGAGTCGGGATCGGGGACGTCGCCCGAGAGCGGGG GGGCGGTGGCGGTGGCGGGAGCCGTTGGGCTGGGTCGGGATCGGGGACGTCGCCCGAGAGCGGGG T C TRIR Ensembl:ENSG00000123144 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:12734442..12734660 26863410 MeRIP-seq:(Medium) rs1177993702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013123,Human_RBP_ID_4557240,Human_RBP_ID_5116711,Human_RBP_ID_5145051,Human_RBP_ID_5321443,Human_RBP_ID_5375798,Human_RBP_ID_8829711,Human_RBP_ID_9328652,Human_RBP_ID_9353584,Human_RBP_ID_17656793,Human_RBP_ID_17915260,Human_RBP_ID_18192006,Human_RBP_ID_18421551,Human_RBP_ID_18722700,Human_RBP_ID_22447452,Human_RBP_ID_22501662,Human_RBP_ID_23130684,Human_RBP_ID_26769994,Human_RBP_ID_27839281 RMVar_hsa_circ_111334,RMVar_hsa_circ_192775 81906 RMVar_ID_81906 Human_SNP_ID_658847468 m1A Human chr19 - 12734662 12734662 12734662 CCTTCCCGGAGTCCTTTGCGCGGCACCTGGCGACAAAATGGCTGCCCGAGGGAGACGGGCGGAGC CCTTCCCGGAGTCCTTTGCGCGGCACCTGGCGCCAAAATGGCTGCCCGAGGGAGACGGGCGGAGC T G TRIR Ensembl:ENSG00000123144 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs981962025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4502699,Human_RBP_ID_8829712,Human_RBP_ID_17915262,Human_RBP_ID_23782803 RMVar_hsa_circ_111334,RMVar_hsa_circ_192775 81907 RMVar_ID_81907 Human_SNP_ID_658848338 m1A Human chr19 + 12737552 12737552 12737552 GGCCGGGTGGGGGGTTGAGGCAGAGGAGTTCGAAGATGCTCCTGATGTGGAGCCGCTGGAGCCTA GGCCGGGTGGGGGGTTGAGGCAGAGGAGTTCGGAGATGCTCCTGATGTGGAGCCGCTGGAGCCTA A G GET3 Ensembl:ENSG00000198356 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:12737501..12737705;chr19:12737501..12737717;chr19:12737501..12738650;chr19:12737501..12737733 26863196 MeRIP-seq:(Medium) rs1568347396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55633,Human_RBP_ID_773013,Human_RBP_ID_4562008,Human_RBP_ID_5116712,Human_RBP_ID_17915263,Human_RBP_ID_18420863,Human_RBP_ID_18945087 Human_Splice_Rec_1963254 81908 RMVar_ID_81908 Human_SNP_ID_658848355 m1A Human chr19 + 12737603 12737603 12737603 GCCGCTGGAGCCTACACTTAGCAACATCATCGAGCAGCGCAGCCTGAAGTGGATCTTCGTCGGGG GCCGCTGGAGCCTACACTTAGCAACATCATCGGGCAGCGCAGCCTGAAGTGGATCTTCGTCGGGG A G GET3 Ensembl:ENSG00000198356 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:12737521..12737614 26863410 MeRIP-seq:(Medium) rs1034277492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554713,Human_RBP_ID_8477349,Human_RBP_ID_23782805 Human_Splice_Rec_1963255,Human_Splice_Rec_1963265,Human_Splice_Rec_1963269 81909 RMVar_ID_81909 Human_SNP_ID_658848592 m1A Human chr19 + 12738453 12738453 12738453 CTGCTCCAGGGAACCTACCACTCCCCTTGCAGACCCAGGGAACAGAGCCCATCCCCTCATCCCCT CTGCTCCAGGGAACCTACCACTCCCCTTGCAGCCCCAGGGAACAGAGCCCATCCCCTCATCCCCT A C GET3 Ensembl:ENSG00000198356 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12738450..12738600 26863196 MeRIP-seq:(Medium) rs1568347599 Functional Loss SNV dbSNP153 33..33 33 - - - 81910 RMVar_ID_81910 Human_SNP_ID_658851438 m1A Human chr19 - 12748073 12748073 12748073 GCTACTGGGCACTGGGGGGCTTGTAGGGCTCCAGGAGGAGGGCCGAGAAGGTGTTGACCTTGTCT GCTACTGGGCACTGGGGGGCTTGTAGGGCTCCTGGAGGAGGGCCGAGAAGGTGTTGACCTTGTCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12748022..12748217 26863196 MeRIP-seq:(Medium) rs1435232254 Functional Loss SNV dbSNP153 33..33 33 - - - 81911 RMVar_ID_81911 Human_SNP_ID_658851441 m1A Human chr19 + 12748082 12748082 12748082 CAACACCTTCTCGGCCCTCCTCCTGGAGCCCTACAAGCCCCCCAGTGCCCAGTAGCACAGCTGCC CAACACCTTCTCGGCCCTCCTCCTGGAGCCCTGCAAGCCCCCCAGTGCCCAGTAGCACAGCTGCC A G GET3 Ensembl:ENSG00000198356 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12747951..12748150 32194978 MeRIP-seq:(Medium) rs1234249260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013132,Human_RBP_ID_17387234,Human_RBP_ID_17656794 RMVar_hsa_circ_83536,RMVar_hsa_circ_81180,RMVar_hsa_circ_117103,RMVar_hsa_circ_192779,RMVar_hsa_circ_192780,RMVar_hsa_circ_122431,RMVar_hsa_circ_192781,RMVar_hsa_circ_192782 81912 RMVar_ID_81912 Human_SNP_ID_658858077 m1A Human chr19 - 12769987 12769987 12769987 CGAGCTGAGGGAGCTGCGGCGGCAGGTGCGGCAGCTGGAGGAACGCAACGCCGGCCACGCCGAGC CGAGCTGAGGGAGCTGCGGCGGCAGGTGCGGCGGCTGGAGGAACGCAACGCCGGCCACGCCGAGC T C HOOK2 Ensembl:ENSG00000095066 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12767878..12771844 26863196 MeRIP-seq:(Medium) rs1568366685 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18996773,Human_RBP_ID_22977416,Human_RBP_ID_27816131 Human_Splice_Rec_1963352,Human_Splice_Rec_1963396,Human_Splice_Rec_1963474 RMVar_hsa_circ_75656,RMVar_hsa_circ_192784,RMVar_hsa_circ_326967 81913 RMVar_ID_81913 Human_SNP_ID_658858393 m1A Human chr19 + 12770986 12770986 12770986 TCAGGGCCTGTGCCTCCTGGGCCAGGCTAGTCAGCGCCTGGTTCCGGTGCTGCAGCTCCGCAACC TCAGGGCCTGTGCCTCCTGGGCCAGGCTAGTCGGCGCCTGGTTCCGGTGCTGCAGCTCCGCAACC A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12767829..12771455 32194978 MeRIP-seq:(Medium) rs1450833594 Functional Loss SNV dbSNP153 33..33 33 - - - 81914 RMVar_ID_81914 Human_SNP_ID_658859300 m1A Human chr19 - 12773547 12773547 12773547 TTCTGGAGACATATGAAGGAAGATGGTCAGGCAGGCCGGGCACAGTGGCTCATGCCTGTAATCCC TTCTGGAGACATATGAAGGAAGATGGTCAGGCCGGCCGGGCACAGTGGCTCATGCCTGTAATCCC T G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12773497..12774083 26863196 MeRIP-seq:(Medium) rs551732055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13371611 81915 RMVar_ID_81915 Human_SNP_ID_658859683 m1A Human chr19 + 12774868 12774868 12774868 GCAAGGCCGCTGCTCAGGTCCTGAGGGCTGGCACAGGGAGACGGAACGTGGAACGTCTGTAACTG GCAAGGCCGCTGCTCAGGTCCTGAGGGCTGGCCCAGGGAGACGGAACGTGGAACGTCTGTAACTG A C RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12774670..12775478 32194978 MeRIP-seq:(Medium) rs1046317733 Functional Loss SNV dbSNP153 33..33 33 - - - 81916 RMVar_ID_81916 Human_SNP_ID_658859918 m1A Human chr19 + 12775498 12775498 12775498 CAATCCAGGCCACGGAGCCCCGGCGCCGCAGCAGCCTCCGGGTCCGCCACCAGCGAGCGCCCGCA CAATCCAGGCCACGGAGCCCCGGCGCCGCAGCGGCCTCCGGGTCCGCCACCAGCGAGCGCCCGCA A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12775377..12775533 26863196 MeRIP-seq:(Medium) rs779436257 Functional Loss SNV dbSNP153 33..33 33 - - - 81917 RMVar_ID_81917 Human_SNP_ID_658864609 m1A Human chr19 - 12791814 12791814 12791814 ACCAGGGGCCCGGCCGTATCCCGTAGCTGTGTATGAGTCGTCGTGGTAGAAGGGCTGTTCCATTT ACCAGGGGCCCGGCCGTATCCCGTAGCTGTGTGTGAGTCGTCGTGGTAGAAGGGCTGTTCCATTT T C HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12791476..12792713 26863196 MeRIP-seq:(Medium) rs780779147 Functional Loss SNV dbSNP153 33..33 33 - - - 81918 RMVar_ID_81918 Human_SNP_ID_658864803 m1A Human chr19 + 12792255 12792255 12792255 ACGTGACACCCCCCAACGTGTCCCTGGGCGCTACCGGGGGGCCCCCGGCTGGGCCCGGGGGCGTC ACGTGACACCCCCCAACGTGTCCCTGGGCGCTGCCGGGGGGCCCCCGGCTGGGCCCGGGGGCGTC A G JUNB Ensembl:ENSG00000171223 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:12792214..12792463 26863196 MeRIP-seq:(Medium) rs1184045320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22069787,Human_RBP_ID_22449228 81919 RMVar_ID_81919 Human_SNP_ID_658866304 m1A Human chr19 + 12797152 12797152 12797152 GTTGGGCTTAATCGTGTCACTGCCAGGCTTCCAGCCAGCGGGACAAACTGTGGGAAGACACAAGG GTTGGGCTTAATCGTGTCACTGCCAGGCTTCCGGCCAGCGGGACAAACTGTGGGAAGACACAAGG A G AC018761.2 Ensembl:ENSG00000267062 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12797151..12797175 26863196 MeRIP-seq:(Medium) rs1413757751 Functional Loss SNV dbSNP153 33..33 33 - - - 81920 RMVar_ID_81920 Human_SNP_ID_658867598 m1A Human chr19 - 12801248 12801248 12801248 GGGGTCTCAGCTTTCAGTCATGGCCTCCGGTAACGCGCGCATCGGAAAGCCAGCCCCTGACTTCA GGGGTCTCAGCTTTCAGTCATGGCCTCCGGTAGCGCGCGCATCGGAAAGCCAGCCCCTGACTTCA T C PRDX2,HOOK2 Ensembl:ENSG00000167815,Ensembl:ENSG00000095066 Protein coding,Protein coding CDS,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:12801201..12801350 26863196 MeRIP-seq:(Medium) rs145783459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772019,Human_RBP_ID_914496,Human_RBP_ID_1554751,Human_RBP_ID_4558114,Human_RBP_ID_5320180,Human_RBP_ID_9328657,Human_RBP_ID_18192010,Human_RBP_ID_22446465 Human_Splice_Rec_1963592,Human_Splice_Rec_1963593,Human_Splice_Rec_1963600,Human_Splice_Rec_1963601,Human_Splice_Rec_1963606,Human_Splice_Rec_1963607,Human_Splice_Rec_1963620,Human_Splice_Rec_1963621 RMVar_hsa_circ_115238,RMVar_hsa_circ_112810,RMVar_hsa_circ_192788,RMVar_hsa_circ_192787,RMVar_hsa_circ_331336,RMVar_hsa_circ_192794 81921 RMVar_ID_81921 Human_SNP_ID_658869127 m1A Human chr19 - 12806665 12806665 12806665 TCTCTCCAGCTCGCTGAGATCCATGCCGCCTCAGCCGCCACCACCAGCTGCAAGAACTAATACTG TCTCTCCAGCTCGCTGAGATCCATGCCGCCTCCGCCGCCACCACCAGCTGCAAGAACTAATACTG T G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12806576..12807001 26863196 MeRIP-seq:(Medium) rs1439892541 Functional Loss SNV dbSNP153 33..33 33 - - - 81922 RMVar_ID_81922 Human_SNP_ID_658869509 m1A Human chr19 - 12807469 12807469 12807469 TGACGTTCACGCCCTGGTCCAATGCATACTGTATAAGCCCAGTGGCTGTATCATGTGACAGGGAG TGACGTTCACGCCCTGGTCCAATGCATACTGTGTAAGCCCAGTGGCTGTATCATGTGACAGGGAG T C HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12807401..12807540 32194978 MeRIP-seq:(Medium) rs150008398 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_423 81923 RMVar_ID_81923 Human_SNP_ID_658871267 m1A Human chr19 + 12813436 12813436 12813436 CGTCCCCGTTCTTCCCACCGATATTTCCTGGAACGCGGCCTGGAGTCAGCAACCAGCCTCTAGCA CGTCCCCGTTCTTCCCACCGATATTTCCTGGAGCGCGGCCTGGAGTCAGCAACCAGCCTCTAGCA A G THSD8,RNASEH2A Ensembl:ENSG00000284491,Ensembl:ENSG00000104889 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12813388..12813481 26863196 MeRIP-seq:(Medium) rs899885314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513518,Human_RBP_ID_1013152,Human_RBP_ID_4502913,Human_RBP_ID_6721079,Human_RBP_ID_17655969,Human_RBP_ID_18722745,Human_RBP_ID_18946541,Human_RBP_ID_22446469,Human_RBP_ID_26983041 RMVar_hsa_circ_192799 81924 RMVar_ID_81924 Human_SNP_ID_658877300 m1A Human chr19 - 12833933 12833933 12833933 CGGCAGCGGCGGCGACTTCGGCCCGGGGAGGGAGGAGGGAGGTAGCGGCGGCGGGAGGAGGGAGG CGGCAGCGGCGGCGACTTCGGCCCGGGGAGGGCGGAGGGAGGTAGCGGCGGCGGGAGGAGGGAGG T G HOOK2,RTBDN Ensembl:ENSG00000095066,Ensembl:ENSG00000132026 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12833924..12834054 26863196 MeRIP-seq:(Medium) rs1020354342 Functional Loss SNV dbSNP153 33..33 33 - - - 81925 RMVar_ID_81925 Human_SNP_ID_658878439 m1A Human chr19 - 12838527 12838518 12838527 CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGAGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG CGACATGGTGGCAGGTGCGGCAGCAGCGGCGG_________CGGCGGCGGCGCGGGGAGCAAGCG GCCGCCGCCT G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12838512..12838620 26863196 MeRIP-seq:(Medium) rs1167311721 Functional Loss DEL dbSNP153 33..41 33 - - - 81926 RMVar_ID_81926 Human_SNP_ID_658878447 m1A Human chr19 - 12838527 12838527 12838527 CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGAGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGGGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG T C HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12838512..12838620 26863196 MeRIP-seq:(Medium) rs746538311 Functional Loss SNV dbSNP153 33..33 33 - - - 81927 RMVar_ID_81927 Human_SNP_ID_658878448 m1A Human chr19 - 12838527 12838527 12838527 CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGAGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG T G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12838512..12838620 26863196 MeRIP-seq:(Medium) rs746538311 Functional Loss SNV dbSNP153 33..33 33 - - - 81928 RMVar_ID_81928 Human_SNP_ID_658879383 m1A Human chr19 - 12842064 12842064 12842064 CATTGCATAGGCACGTAATCCCTCACACAGTGACAATCACACACACACACCAGCACACTTTGCAC CATTGCATAGGCACGTAATCCCTCACACAGTGGCAATCACACACACACACCAGCACACTTTGCAC T C HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12842062..12842197 26863196 MeRIP-seq:(Medium) rs931465947 Functional Loss SNV dbSNP153 33..33 33 - - - 81929 RMVar_ID_81929 Human_SNP_ID_658879384 m1A Human chr19 - 12842064 12842064 12842064 CATTGCATAGGCACGTAATCCCTCACACAGTGACAATCACACACACACACCAGCACACTTTGCAC CATTGCATAGGCACGTAATCCCTCACACAGTGCCAATCACACACACACACCAGCACACTTTGCAC T G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12842062..12842197 26863196 MeRIP-seq:(Medium) rs931465947 Functional Loss SNV dbSNP153 33..33 33 - - - 81930 RMVar_ID_81930 Human_SNP_ID_658888640 m1A Human chr19 - 12875709 12875707 12875709 GGTCACATAGCAAGACTCTGTTTCAAAAAAAAAGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT GGTCACATAGCAAGACTCTGTTTCAAAAAAAA__GGGGGGCGGGGGACGGGTGGGTGCAGTGGCT CCT C DNASE2 Ensembl:ENSG00000105612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1491464664 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5145671,Human_RBP_ID_8198599,Human_RBP_ID_17386683,Human_RBP_ID_26472078 Human_miRNA_ID_1967484 RMVar_hsa_circ_82172,RMVar_hsa_circ_192813 81931 RMVar_ID_81931 Human_SNP_ID_658888642 m1A Human chr19 - 12875709 12875708 12875709 GGTCACATAGCAAGACTCTGTTTCAAAAAAAAAGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT GGTCACATAGCAAGACTCTGTTTCAAAAAAAA_GGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT CT C DNASE2 Ensembl:ENSG00000105612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs113410270 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5145671,Human_RBP_ID_8198599,Human_RBP_ID_17386683,Human_RBP_ID_26472078 Human_miRNA_ID_1967484 RMVar_hsa_circ_82172,RMVar_hsa_circ_192813 81932 RMVar_ID_81932 Human_SNP_ID_658888645 m1A Human chr19 - 12875709 12875709 12875709 GGTCACATAGCAAGACTCTGTTTCAAAAAAAAAGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT GGTCACATAGCAAGACTCTGTTTCAAAAAAAAGGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT T C DNASE2 Ensembl:ENSG00000105612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs537971974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145671,Human_RBP_ID_8198599,Human_RBP_ID_17386683,Human_RBP_ID_26472078 Human_miRNA_ID_1967484 RMVar_hsa_circ_82172,RMVar_hsa_circ_192813 81933 RMVar_ID_81933 Human_SNP_ID_658889432 m1A Human chr19 - 12878717 12878717 12878717 CAGCTGGCCTCATAGCGCCTGTACCTACGGGCAGACCCTGCTCTGTGTGTCTTTTCCCTTCGCTC CAGCTGGCCTCATAGCGCCTGTACCTACGGGCCGACCCTGCTCTGTGTGTCTTTTCCCTTCGCTC T G DNASE2 Ensembl:ENSG00000105612 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12878651..12878750 32194978 MeRIP-seq:(Medium) rs1168262254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770929,Human_RBP_ID_17386684,Human_RBP_ID_22763278 Human_Splice_Rec_1963977,Human_Splice_Rec_1963991 Human_miRNA_ID_2455871 RMVar_hsa_circ_192814,RMVar_hsa_circ_76683,RMVar_hsa_circ_82172,RMVar_hsa_circ_192813,RMVar_hsa_circ_287910,RMVar_hsa_circ_192815 81934 RMVar_ID_81934 Human_SNP_ID_658890143 m1A Human chr19 - 12881062 12881062 12881062 CTGCAGTACAAGTATCTGGACGAGAGCTCCGGAGGCTGGCGGGACGGCAGGGCACTCATCAACAG CTGCAGTACAAGTATCTGGACGAGAGCTCCGGCGGCTGGCGGGACGGCAGGGCACTCATCAACAG T G DNASE2 Ensembl:ENSG00000105612 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:12881015..12881163;chr19:12881013..12881106;chr19:12881013..12881151 26863196,32194978,32194978 MeRIP-seq:(Medium) rs757807054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770930,Human_RBP_ID_913564,Human_RBP_ID_4559269,Human_RBP_ID_22446473,Human_RBP_ID_22763282 Human_Splice_Rec_1963972,Human_Splice_Rec_1963973,Human_Splice_Rec_1963984,Human_Splice_Rec_1963985 RMVar_hsa_circ_76683,RMVar_hsa_circ_192815 81935 RMVar_ID_81935 Human_SNP_ID_658893187 m1A Human chr19 + 12891314 12891312 12891314 TGCTCCGCTCGCTCTGAGAGAGCATGGCCCTGAGAGGCGTCTCCGTGCGGCTGCTGAGCCGCGGA TGCTCCGCTCGCTCTGAGAGAGCATGGCCCT__GAGGCGTCTCCGTGCGGCTGCTGAGCCGCGGA TGA T GCDH Ensembl:ENSG00000105607 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12891199..12891352 26863196 MeRIP-seq:(Medium) rs762136250 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4558127 Human_Splice_Rec_1964000,Human_Splice_Rec_1964001,Human_Splice_Rec_1964010,Human_Splice_Rec_1964011,Human_Splice_Rec_1964023,Human_Splice_Rec_1964044,Human_Splice_Rec_1964045,Human_Splice_Rec_1964066,Human_Splice_Rec_1964067,Human_Splice_Rec_1964074,Human_Splice_Rec_1964075,Human_Splice_Rec_1964096,Human_Splice_Rec_1964097,Human_Splice_Rec_1964106,Human_Splice_Rec_1964107,Human_Splice_Rec_1964118,Human_Splice_Rec_1964119,Human_Splice_Rec_1964126,Human_Splice_Rec_1964127,Human_Splice_Rec_1964136,Human_Splice_Rec_1964137,Human_Splice_Rec_1964155,Human_Splice_Rec_1964161 Human_miRNA_ID_2354373,Human_miRNA_ID_2574906 RMVar_hsa_circ_81275,RMVar_hsa_circ_377997,RMVar_hsa_circ_192817 81936 RMVar_ID_81936 Human_SNP_ID_658893202 m1A Human chr19 + 12891338 12891338 12891338 TGGCCCTGAGAGGCGTCTCCGTGCGGCTGCTGAGCCGCGGACCCGGCCTGCACGTCCTTCGCACG TGGCCCTGAGAGGCGTCTCCGTGCGGCTGCTGTGCCGCGGACCCGGCCTGCACGTCCTTCGCACG A T GCDH Ensembl:ENSG00000105607 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12891245..12891525 26863196 MeRIP-seq:(Medium) rs781063858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558127 Human_Splice_Rec_1964000,Human_Splice_Rec_1964001,Human_Splice_Rec_1964010,Human_Splice_Rec_1964011,Human_Splice_Rec_1964023,Human_Splice_Rec_1964044,Human_Splice_Rec_1964045,Human_Splice_Rec_1964066,Human_Splice_Rec_1964067,Human_Splice_Rec_1964074,Human_Splice_Rec_1964075,Human_Splice_Rec_1964096,Human_Splice_Rec_1964097,Human_Splice_Rec_1964106,Human_Splice_Rec_1964107,Human_Splice_Rec_1964118,Human_Splice_Rec_1964119,Human_Splice_Rec_1964126,Human_Splice_Rec_1964127,Human_Splice_Rec_1964136,Human_Splice_Rec_1964137,Human_Splice_Rec_1964155,Human_Splice_Rec_1964161 Human_miRNA_ID_2270457 RMVar_hsa_circ_81275,RMVar_hsa_circ_377997,RMVar_hsa_circ_192817 81937 RMVar_ID_81937 Human_SNP_ID_658893215 m1A Human chr19 + 12891357 12891357 12891357 CGTGCGGCTGCTGAGCCGCGGACCCGGCCTGCACGTCCTTCGCACGTGGGTCTCGTCGGCGGCGC CGTGCGGCTGCTGAGCCGCGGACCCGGCCTGCCCGTCCTTCGCACGTGGGTCTCGTCGGCGGCGC A C GCDH Ensembl:ENSG00000105607 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12891240..12891427 26863196 MeRIP-seq:(Medium) rs775848834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558127,Human_RBP_ID_18996790 Human_Splice_Rec_1964000,Human_Splice_Rec_1964001,Human_Splice_Rec_1964010,Human_Splice_Rec_1964011,Human_Splice_Rec_1964023,Human_Splice_Rec_1964044,Human_Splice_Rec_1964045,Human_Splice_Rec_1964066,Human_Splice_Rec_1964067,Human_Splice_Rec_1964074,Human_Splice_Rec_1964075,Human_Splice_Rec_1964096,Human_Splice_Rec_1964097,Human_Splice_Rec_1964106,Human_Splice_Rec_1964107,Human_Splice_Rec_1964118,Human_Splice_Rec_1964119,Human_Splice_Rec_1964126,Human_Splice_Rec_1964127,Human_Splice_Rec_1964136,Human_Splice_Rec_1964137,Human_Splice_Rec_1964155,Human_Splice_Rec_1964161 RMVar_hsa_circ_81275,RMVar_hsa_circ_377997,RMVar_hsa_circ_192817 81938 RMVar_ID_81938 Human_SNP_ID_658893351 m1A Human chr19 + 12891646 12891646 12891646 CCGAGCGGGGTGGCAGGGTCGTGGCCAGGGTCAGAGGCACTAAGGCAGTGAGTGCGCTGTGCCTG CCGAGCGGGGTGGCAGGGTCGTGGCCAGGGTCTGAGGCACTAAGGCAGTGAGTGCGCTGTGCCTG A T GCDH Ensembl:ENSG00000105607 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12891644..12891820 26863196 MeRIP-seq:(Medium) rs922305439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55164,Human_RBP_ID_513562,Human_RBP_ID_21977722 Human_Splice_Rec_1964069 RMVar_hsa_circ_377997 81939 RMVar_ID_81939 Human_SNP_ID_658897378 m1A Human chr19 - 12904593 12904593 12904593 TCTACTTCTCCTCTCTGGACTCAAGCATTGACATCCTGCAGAAGAGAGCCCAGGAGCTGATCGAA TCTACTTCTCCTCTCTGGACTCAAGCATTGACTTCCTGCAGAAGAGAGCCCAGGAGCTGATCGAA T A SYCE2 Ensembl:ENSG00000161860 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12900570..12904608 32194978 MeRIP-seq:(Medium) rs1216603951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1964192 RMVar_hsa_circ_3312,RMVar_hsa_circ_365286 81940 RMVar_ID_81940 Human_SNP_ID_658903141 m1A Human chr19 - 12924777 12924777 12924777 AGAAGCCCTTCACTCCGGTCAAGTACTTCTCCATCGACCGCGTATTCCGGAATGAGACCCTGGAC AGAAGCCCTTCACTCCGGTCAAGTACTTCTCCGTCGACCGCGTATTCCGGAATGAGACCCTGGAC T C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12924726..12924800 32194978 MeRIP-seq:(Medium) rs1335372478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1880241,Human_RBP_ID_3563338,Human_RBP_ID_18722807,Human_RBP_ID_26815347 Human_Splice_Rec_1964220,Human_Splice_Rec_1964246,Human_Splice_Rec_1964268,Human_Splice_Rec_1964292,Human_Splice_Rec_1964326,Human_Splice_Rec_1964340 RMVar_hsa_circ_24871,RMVar_hsa_circ_109494,RMVar_hsa_circ_192819,RMVar_hsa_circ_77885,RMVar_hsa_circ_114698,RMVar_hsa_circ_326312,RMVar_hsa_circ_192820,RMVar_hsa_circ_98841,RMVar_hsa_circ_192822,RMVar_hsa_circ_106605,RMVar_hsa_circ_192821,RMVar_hsa_circ_82781,RMVar_hsa_circ_192823,RMVar_hsa_circ_192824 81941 RMVar_ID_81941 Human_SNP_ID_658903223 m1A Human chr19 + 12924962 12924962 12924962 GGGCGCTGGCTGATGTGGTGTGGGTTCGCAGTAGGTTTTTCCGGGCCTCGTCCAGCTTCCAGTTA GGGCGCTGGCTGATGTGGTGTGGGTTCGCAGTGGGTTTTTCCGGGCCTCGTCCAGCTTCCAGTTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:12924832..12925175;chr19:12924901..12925025 26863196 MeRIP-seq:(Medium) rs1489303167 Functional Loss SNV dbSNP153 33..33 33 - - - 81942 RMVar_ID_81942 Human_SNP_ID_658903234 m1A Human chr19 + 12924983 12924983 12924983 GGGTTCGCAGTAGGTTTTTCCGGGCCTCGTCCAGCTTCCAGTTATACTTGTACCTTCAGGAGGGA GGGTTCGCAGTAGGTTTTTCCGGGCCTCGTCCGGCTTCCAGTTATACTTGTACCTTCAGGAGGGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12924676..12925025 26863196 MeRIP-seq:(Medium) rs142135169 Functional Loss SNV dbSNP153 33..33 33 - - - 81943 RMVar_ID_81943 Human_SNP_ID_658903295 m1A Human chr19 + 12925138 12925138 12925138 CGCCCTGAGAGTGGGTCCGCTTGACCCGCTGGACATAGTCCATTGGGAGCTGCAGGGCCTCCGCT CGCCCTGAGAGTGGGTCCGCTTGACCCGCTGGGCATAGTCCATTGGGAGCTGCAGGGCCTCCGCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12925076..12925175 26863196 MeRIP-seq:(Medium) rs772355851 Functional Loss SNV dbSNP153 33..33 33 - - - 81944 RMVar_ID_81944 Human_SNP_ID_658903296 m1A Human chr19 + 12925138 12925138 12925138 CGCCCTGAGAGTGGGTCCGCTTGACCCGCTGGACATAGTCCATTGGGAGCTGCAGGGCCTCCGCT CGCCCTGAGAGTGGGTCCGCTTGACCCGCTGGTCATAGTCCATTGGGAGCTGCAGGGCCTCCGCT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12925076..12925175 26863196 MeRIP-seq:(Medium) rs772355851 Functional Loss SNV dbSNP153 33..33 33 - - - 81945 RMVar_ID_81945 Human_SNP_ID_658904463 m1A Human chr19 - 12928801 12928801 12928801 ACTGGGTGAGCAAAGGCAGTGCCTTTAGTACCAGCATCTCCAAGCAAGAGACAGAGCTGAGCCCA ACTGGGTGAGCAAAGGCAGTGCCTTTAGTACCGGCATCTCCAAGCAAGAGACAGAGCTGAGCCCA T C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12928776..12928800 32194978 MeRIP-seq:(Medium) rs892791704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554844,Human_RBP_ID_1880244,Human_RBP_ID_3956406,Human_RBP_ID_18994434 Human_Splice_Rec_1964210,Human_Splice_Rec_1964211,Human_Splice_Rec_1964236,Human_Splice_Rec_1964237,Human_Splice_Rec_1964282,Human_Splice_Rec_1964283,Human_Splice_Rec_1964306,Human_Splice_Rec_1964307,Human_Splice_Rec_1964330,Human_Splice_Rec_1964331,Human_Splice_Rec_1964352,Human_Splice_Rec_1964353,Human_Splice_Rec_1964360,Human_Splice_Rec_1964361 Human_miRNA_ID_1985452,Human_miRNA_ID_1985453,Human_miRNA_ID_2616230,Human_miRNA_ID_2616231,Human_miRNA_ID_2941096,Human_miRNA_ID_2941097 RMVar_hsa_circ_192819,RMVar_hsa_circ_77885,RMVar_hsa_circ_326312,RMVar_hsa_circ_192822,RMVar_hsa_circ_106605,RMVar_hsa_circ_82781,RMVar_hsa_circ_125133,RMVar_hsa_circ_85645,RMVar_hsa_circ_192823,RMVar_hsa_circ_192827,RMVar_hsa_circ_339360,RMVar_hsa_circ_270151,RMVar_hsa_circ_110150,RMVar_hsa_circ_192830,RMVar_hsa_circ_192832,RMVar_hsa_circ_192833,RMVar_hsa_circ_192831,RMVar_hsa_circ_192829,RMVar_hsa_circ_108569,RMVar_hsa_circ_192834,RMVar_hsa_circ_370516,RMVar_hsa_circ_192835 81946 RMVar_ID_81946 Human_SNP_ID_658904478 m1A Human chr19 - 12928849 12928849 12928849 GGCAGTGGCGTCCCCTTCCTTCCCCTGGCCACAGGACTCTGAAGACCTACTGGGTGAGCAAAGGC GGCAGTGGCGTCCCCTTCCTTCCCCTGGCCACGGGACTCTGAAGACCTACTGGGTGAGCAAAGGC T C FARSA Ensembl:ENSG00000179115 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:12928293..12928894;chr19:12928318..12928893;chr19:12928551..12928850 26863196 MeRIP-seq:(Medium) rs1362149931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910751,Human_RBP_ID_5373273,Human_RBP_ID_22546640 Human_Splice_Rec_1964211,Human_Splice_Rec_1964237,Human_Splice_Rec_1964283,Human_Splice_Rec_1964307,Human_Splice_Rec_1964331,Human_Splice_Rec_1964353,Human_Splice_Rec_1964361 RMVar_hsa_circ_125133,RMVar_hsa_circ_339360,RMVar_hsa_circ_110150,RMVar_hsa_circ_192830,RMVar_hsa_circ_192832,RMVar_hsa_circ_192833,RMVar_hsa_circ_192831 81947 RMVar_ID_81947 Human_SNP_ID_658905039 m1A Human chr19 + 12930733 12930733 12930733 CCGCAGTAAGCTCCCAGTGCTTGGTGGACCGAAGTTCAGCCTCGATGACCTAGAGGGAAATGTGG CCGCAGTAAGCTCCCAGTGCTTGGTGGACCGACGTTCAGCCTCGATGACCTAGAGGGAAATGTGG A C FARSA-AS1 Ensembl:ENSG00000266975 lincRNA intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:12930726..12930750;chr19:12930601..12930750 26863196 MeRIP-seq:(Medium) rs1216432088 Functional Loss SNV dbSNP153 33..33 33 - - - 81948 RMVar_ID_81948 Human_SNP_ID_658905041 m1A Human chr19 - 12930742 12930742 12930742 ACACCCTCCCCACATTTCCCTCTAGGTCATCGAGGCTGAACTTCGGTCCACCAAGCACTGGGAGC ACACCCTCCCCACATTTCCCTCTAGGTCATCGGGGCTGAACTTCGGTCCACCAAGCACTGGGAGC T C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:12930189..12930797;chr19:12930197..12930775 26863196 MeRIP-seq:(Medium) rs755195431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554848,Human_RBP_ID_4503110 Human_Splice_Rec_1964204,Human_Splice_Rec_1964230,Human_Splice_Rec_1964254,Human_Splice_Rec_1964276,Human_Splice_Rec_1964300,Human_Splice_Rec_1964346,Human_Splice_Rec_1964356,Human_Splice_Rec_1964366 RMVar_hsa_circ_339360,RMVar_hsa_circ_110150,RMVar_hsa_circ_192832,RMVar_hsa_circ_192833 81949 RMVar_ID_81949 Human_SNP_ID_658905801 m1A Human chr19 - 12933630 12933630 12933630 GGCGGCTGGAGGCGTCTGATGGCGGCCTGGACAGCGCCGAGTTGGCGGCTGAGCTGGGCATGGAG GGCGGCTGGAGGCGTCTGATGGCGGCCTGGACGGCGCCGAGTTGGCGGCTGAGCTGGGCATGGAG T C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12933551..12933675 32194978 MeRIP-seq:(Medium) rs747427583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5320187,Human_RBP_ID_9328666,Human_RBP_ID_9380583,Human_RBP_ID_17131697,Human_RBP_ID_22447460,Human_RBP_ID_22742432,Human_RBP_ID_23119121,Human_RBP_ID_23210874 Human_Splice_Rec_1964203,Human_Splice_Rec_1964228,Human_Splice_Rec_1964229,Human_Splice_Rec_1964253,Human_Splice_Rec_1964275,Human_Splice_Rec_1964299,Human_Splice_Rec_1964327,Human_Splice_Rec_1964345,Human_Splice_Rec_1964355,Human_Splice_Rec_1964365 Human_miRNA_ID_3010987 RMVar_hsa_circ_110150,RMVar_hsa_circ_192833 81950 RMVar_ID_81950 Human_SNP_ID_658905817 m1A Human chr19 + 12933671 12933671 12933671 CGCCATCAGACGCCTCCAGCCGCCGGAGCAGCAGTTCCGCCACCTGACCATCCGCCATGACTCCT CGCCATCAGACGCCTCCAGCCGCCGGAGCAGCCGTTCCGCCACCTGACCATCCGCCATGACTCCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:12933551..12933700 26863196 MeRIP-seq:(Medium) rs1353583528 Functional Loss SNV dbSNP153 33..33 33 - - - 81951 RMVar_ID_81951 Human_SNP_ID_658905818 m1A Human chr19 + 12933671 12933671 12933671 CGCCATCAGACGCCTCCAGCCGCCGGAGCAGCAGTTCCGCCACCTGACCATCCGCCATGACTCCT CGCCATCAGACGCCTCCAGCCGCCGGAGCAGCGGTTCCGCCACCTGACCATCCGCCATGACTCCT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:12933551..12933700 26863196 MeRIP-seq:(Medium) rs1353583528 Functional Loss SNV dbSNP153 33..33 33 - - - 81952 RMVar_ID_81952 Human_SNP_ID_658907320 m1A Human chr19 - 12938660 12938660 12938660 CGGATAGCAGCATGGCGGGCCGAGGGGGCGGCAACGCGCGGGCCCTTTAAAACGACCCTCCGGCA CGGATAGCAGCATGGCGGGCCGAGGGGGCGGCGACGCGCGGGCCCTTTAAAACGACCCTCCGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:12938601..12938824;chr19:12938601..12938827;chr19:12938601..12938875 26863196 MeRIP-seq:(Medium) rs1328680505 Functional Loss SNV dbSNP153 33..33 33 - - - 81953 RMVar_ID_81953 Human_SNP_ID_658907747 m1A Human chr19 - 12939628 12939627 12939628 GAGATCAGCACCAGGAAGCAGGCCCTCACCAAACATGATGTTGTATTCTGAGTCTCCGTGCATGT GAGATCAGCACCAGGAAGCAGGCCCTCACCAA_CATGATGTTGTATTCTGAGTCTCCGTGCATGT GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12939398..12939657 26863196 MeRIP-seq:(Medium) rs1393842839 Functional Loss DEL dbSNP153 33..33 33 - - - 81954 RMVar_ID_81954 Human_SNP_ID_658908145 m1A Human chr19 + 12940650 12940650 12940650 GTGGGAACCCCCAGTGATTCAGAACCCTGAGTACAAGGTGAGTTTGGGGCTCTGAGCAGGGCTGG GTGGGAACCCCCAGTGATTCAGAACCCTGAGTGCAAGGTGAGTTTGGGGCTCTGAGCAGGGCTGG A G CALR Ensembl:ENSG00000179218 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12940526..12940650 32194978 MeRIP-seq:(Medium) rs1226804338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513616,Human_RBP_ID_914235,Human_RBP_ID_5588305,Human_RBP_ID_8477496,Human_RBP_ID_9380601,Human_RBP_ID_13372384,Human_RBP_ID_17694629,Human_RBP_ID_18470518,Human_RBP_ID_22446495,Human_RBP_ID_22763306,Human_RBP_ID_24552815,Human_RBP_ID_26334872,Human_RBP_ID_27816141 Human_Splice_Rec_1964387,Human_Splice_Rec_1964407,Human_Splice_Rec_1964411 Human_miRNA_ID_2771311 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_77416,RMVar_hsa_circ_192836,RMVar_hsa_circ_369902,RMVar_hsa_circ_106916,RMVar_hsa_circ_192839,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_9148,RMVar_hsa_circ_88629,RMVar_hsa_circ_110485,RMVar_hsa_circ_192842,RMVar_hsa_circ_192843,RMVar_hsa_circ_105835,RMVar_hsa_circ_331796,RMVar_hsa_circ_192844,RMVar_hsa_circ_192845,RMVar_hsa_circ_192846,RMVar_hsa_circ_361141,RMVar_hsa_circ_364158,RMVar_hsa_circ_64986,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_103183,RMVar_hsa_circ_192848,RMVar_hsa_circ_192849 81955 RMVar_ID_81955 Human_SNP_ID_658909353 m1A Human chr19 - 12943952 12943952 12943952 ACATTATTTGGCGCGGCCAGCTCTGCGGCAGGAGCGCTCAGGCCTCAGTCCAGCCCTGGAGGCAG ACATTATTTGGCGCGGCCAGCTCTGCGGCAGGGGCGCTCAGGCCTCAGTCCAGCCCTGGAGGCAG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:12943791..12943964 26863410 MeRIP-seq:(Medium) rs758391484 Functional Loss SNV dbSNP153 33..33 33 - - - 81956 RMVar_ID_81956 Human_SNP_ID_658910115 m1A Human chr19 - 12945937 12945921 12945938 GAGCGTGATGGTGACGGCCATGGCGGGGCCCGAGCGACGCGGCGGCCCCGGGATCCTCACACAAC GAGCGTGATGGTGACGGCCATGGCGGGGCCC_________________CGGGATCCTCACACAAC GGGGCCGCCGCGTCGCTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:12945851..12946060;chr19:12945851..12946061 26863196 MeRIP-seq:(Medium) rs1476875627 Functional Loss DEL dbSNP153 32..48 33 - - - 81957 RMVar_ID_81957 Human_SNP_ID_658910870 m1A Human chr19 - 12948198 12948198 12948198 GGCAGCTGTGGGTGAGGCCTCTGGGGGTGCTGAGGTACCCTGGCCGGCTTTGGTCTGCAACAGCA GGCAGCTGTGGGTGAGGCCTCTGGGGGTGCTGCGGTACCCTGGCCGGCTTTGGTCTGCAACAGCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12947983..12948207 26863196 MeRIP-seq:(Medium) rs1286422563 Functional Loss SNV dbSNP153 33..33 33 - - - 81958 RMVar_ID_81958 Human_SNP_ID_658910923 m1A Human chr19 + 12948333 12948333 12948333 AGGACAAGAGCCCATCAGAGGAATCCGCCCCCACGACGTCCCCAGAGTCTGTGTCAGGGTAAGGC AGGACAAGAGCCCATCAGAGGAATCCGCCCCCGCGACGTCCCCAGAGTCTGTGTCAGGGTAAGGC A G RAD23A Ensembl:ENSG00000179262 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12948282..12948444 26863196 MeRIP-seq:(Medium) rs11558955 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_513663,Human_RBP_ID_772193,Human_RBP_ID_826039,Human_RBP_ID_3954555,Human_RBP_ID_17915393 Human_Splice_Rec_1964427,Human_Splice_Rec_1964441,Human_Splice_Rec_1964457,Human_Splice_Rec_1964473,Human_Splice_Rec_1964483,Human_Splice_Rec_1964499,Human_Splice_Rec_1964513,Human_Splice_Rec_1964529 Human_miRNA_ID_2425597,Human_miRNA_ID_2435265,Human_miRNA_ID_2784715 GWAS_ID_9621,GWAS_ID_9622,GWAS_ID_9623,GWAS_ID_9624 RMVar_hsa_circ_425,RMVar_hsa_circ_192856,RMVar_hsa_circ_315860 81959 RMVar_ID_81959 Human_SNP_ID_658911103 m1A Human chr19 + 12948746 12948746 12948746 GACGGAGATCATGTCCATGGGCTATGAGCGAGAGCGGGTCGTGGCCGCCCTGAGAGCCAGCTACA GACGGAGATCATGTCCATGGGCTATGAGCGAGCGCGGGTCGTGGCCGCCCTGAGAGCCAGCTACA A C RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12948676..12948775 26863196 MeRIP-seq:(Medium) rs565619875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241882,Human_RBP_ID_513667,Human_RBP_ID_1554915,Human_RBP_ID_1880293,Human_RBP_ID_4562235,Human_RBP_ID_8829753,Human_RBP_ID_9328670,Human_RBP_ID_9380624,Human_RBP_ID_13372584,Human_RBP_ID_17670221,Human_RBP_ID_25384636 Human_Splice_Rec_1964428,Human_Splice_Rec_1964429,Human_Splice_Rec_1964444,Human_Splice_Rec_1964445,Human_Splice_Rec_1964460,Human_Splice_Rec_1964461,Human_Splice_Rec_1964476,Human_Splice_Rec_1964486,Human_Splice_Rec_1964487,Human_Splice_Rec_1964502,Human_Splice_Rec_1964503,Human_Splice_Rec_1964516,Human_Splice_Rec_1964517,Human_Splice_Rec_1964532,Human_Splice_Rec_1964533,Human_Splice_Rec_1964539 Human_miRNA_ID_336528,Human_miRNA_ID_794325 81960 RMVar_ID_81960 Human_SNP_ID_658911104 m1A Human chr19 + 12948746 12948746 12948746 GACGGAGATCATGTCCATGGGCTATGAGCGAGAGCGGGTCGTGGCCGCCCTGAGAGCCAGCTACA GACGGAGATCATGTCCATGGGCTATGAGCGAGGGCGGGTCGTGGCCGCCCTGAGAGCCAGCTACA A G RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12948676..12948775 26863196 MeRIP-seq:(Medium) rs565619875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241882,Human_RBP_ID_513667,Human_RBP_ID_1554915,Human_RBP_ID_1880293,Human_RBP_ID_4562235,Human_RBP_ID_8829753,Human_RBP_ID_9328670,Human_RBP_ID_9380624,Human_RBP_ID_13372584,Human_RBP_ID_17670221,Human_RBP_ID_25384636 Human_Splice_Rec_1964428,Human_Splice_Rec_1964429,Human_Splice_Rec_1964444,Human_Splice_Rec_1964445,Human_Splice_Rec_1964460,Human_Splice_Rec_1964461,Human_Splice_Rec_1964476,Human_Splice_Rec_1964486,Human_Splice_Rec_1964487,Human_Splice_Rec_1964502,Human_Splice_Rec_1964503,Human_Splice_Rec_1964516,Human_Splice_Rec_1964517,Human_Splice_Rec_1964532,Human_Splice_Rec_1964533,Human_Splice_Rec_1964539 Human_miRNA_ID_336528,Human_miRNA_ID_794325 81961 RMVar_ID_81961 Human_SNP_ID_658911238 m1A Human chr19 + 12949130 12949130 12949130 CGAGCCGGAACACGGTTCTGTCCAGGAGAGCCAGGTATCGGAGCAGCCGGCCACGGAAGCAGGTG CGAGCCGGAACACGGTTCTGTCCAGGAGAGCCGGGTATCGGAGCAGCCGGCCACGGAAGCAGGTG A G RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12949076..12949400 32194978 MeRIP-seq:(Medium) rs1205455830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17915397,Human_RBP_ID_19089407 Human_Splice_Rec_1964430,Human_Splice_Rec_1964431,Human_Splice_Rec_1964446,Human_Splice_Rec_1964447,Human_Splice_Rec_1964462,Human_Splice_Rec_1964463,Human_Splice_Rec_1964477,Human_Splice_Rec_1964488,Human_Splice_Rec_1964489,Human_Splice_Rec_1964504,Human_Splice_Rec_1964505,Human_Splice_Rec_1964518,Human_Splice_Rec_1964519,Human_Splice_Rec_1964534,Human_Splice_Rec_1964535,Human_Splice_Rec_1964545 Human_miRNA_ID_336529,Human_miRNA_ID_794326 81962 RMVar_ID_81962 Human_SNP_ID_658911335 m1A Human chr19 - 12949351 12949351 12949351 CCCAGCTGCTGGAGCAGGGCGGGCAGCAGCGCAGGGTTCTGCTGAATCACCTGCCGCATGTTCTG CCCAGCTGCTGGAGCAGGGCGGGCAGCAGCGCGGGGTTCTGCTGAATCACCTGCCGCATGTTCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12949034..12949524 26863196 MeRIP-seq:(Medium) rs190497908 Functional Loss SNV dbSNP153 33..33 33 - - - 81963 RMVar_ID_81963 Human_SNP_ID_658912389 m1A Human chr19 + 12952795 12952795 12952795 TGTGGAGGGGGAGGTGGGCGCCATAGGAGAGGAGGCCCCGCAGATGAACTACATCCAGGTGACGC TGTGGAGGGGGAGGTGGGCGCCATAGGAGAGGCGGCCCCGCAGATGAACTACATCCAGGTGACGC A C RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12952744..12953023 26863196 MeRIP-seq:(Medium) rs1401343234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55567,Human_RBP_ID_513673,Human_RBP_ID_772891,Human_RBP_ID_1013189,Human_RBP_ID_5320188,Human_RBP_ID_5585375,Human_RBP_ID_22977670,Human_RBP_ID_23114764,Human_RBP_ID_23130714,Human_RBP_ID_23783111 Human_Splice_Rec_1964435,Human_Splice_Rec_1964451,Human_Splice_Rec_1964467,Human_Splice_Rec_1964493,Human_Splice_Rec_1964523,Human_Splice_Rec_1964543,Human_Splice_Rec_1964549,Human_Splice_Rec_1964551 Human_miRNA_ID_1091017 RMVar_hsa_circ_41260 81964 RMVar_ID_81964 Human_SNP_ID_658912482 m1A Human chr19 + 12953054 12953054 12953054 CCTGAGTCAGAACTTTGATGACGAGTGATGCCAGGAAGCCAGGCCACCGAAGCCCCCACCCTACC CCTGAGTCAGAACTTTGATGACGAGTGATGCCGGGAAGCCAGGCCACCGAAGCCCCCACCCTACC A G RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12952923..12953445 26863196 MeRIP-seq:(Medium) rs1161322799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513679,Human_RBP_ID_1554922,Human_RBP_ID_1880295,Human_RBP_ID_4503272,Human_RBP_ID_23783113,Human_RBP_ID_25384673 Human_miRNA_ID_254432,Human_miRNA_ID_794327 81965 RMVar_ID_81965 Human_SNP_ID_658912557 m1A Human chr19 + 12953240 12953240 12953240 AAAGTGGCCCCTGTTCCCATCTCCCGGGCCAGACAGCTGTCCCCCCGTCCTCCTCCCCAGCCCAG AAAGTGGCCCCTGTTCCCATCTCCCGGGCCAGGCAGCTGTCCCCCCGTCCTCCTCCCCAGCCCAG A G RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12953190..12953402 26863196 MeRIP-seq:(Medium) rs548294453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241885,Human_RBP_ID_513684,Human_RBP_ID_4503283,Human_RBP_ID_17656823,Human_RBP_ID_18192024,Human_RBP_ID_18946552 81966 RMVar_ID_81966 Human_SNP_ID_658913007 m1A Human chr19 - 12954498 12954498 12954498 GCAGGGAGCAGCACATCGCAGAGTGCATGGCCAAGATGCCACAGATGATTGTGAACTGGCAGCAG GCAGGGAGCAGCACATCGCAGAGTGCATGGCCGAGATGCCACAGATGATTGTGAACTGGCAGCAG T C GADD45GIP1 Ensembl:ENSG00000179271 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12954451..12954550 32194978 MeRIP-seq:(Medium) rs1010745578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54593,Human_RBP_ID_513710,Human_RBP_ID_908479,Human_RBP_ID_1554934,Human_RBP_ID_9084559,Human_RBP_ID_19089409,Human_RBP_ID_26337541,Human_RBP_ID_27815194 Human_Splice_Rec_1964554 Human_miRNA_ID_2393824 RMVar_hsa_circ_111961,RMVar_hsa_circ_124765,RMVar_hsa_circ_192857,RMVar_hsa_circ_192858,RMVar_hsa_circ_192859 81967 RMVar_ID_81967 Human_SNP_ID_658913008 m1A Human chr19 - 12954504 12954504 12954504 TCCCCTGCAGGGAGCAGCACATCGCAGAGTGCATGGCCAAGATGCCACAGATGATTGTGAACTGG TCCCCTGCAGGGAGCAGCACATCGCAGAGTGCGTGGCCAAGATGCCACAGATGATTGTGAACTGG T C GADD45GIP1 Ensembl:ENSG00000179271 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr19:12954476..12954525;chr19:12954347..12954566 26863196 MeRIP-seq:(Medium) rs762239065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54593,Human_RBP_ID_513711,Human_RBP_ID_910759,Human_RBP_ID_1554934,Human_RBP_ID_4562272,Human_RBP_ID_9084559,Human_RBP_ID_19089409,Human_RBP_ID_26337541,Human_RBP_ID_27815194 Human_Splice_Rec_1964554 Human_miRNA_ID_2393824 RMVar_hsa_circ_111961,RMVar_hsa_circ_124765,RMVar_hsa_circ_192857,RMVar_hsa_circ_192858,RMVar_hsa_circ_192859 81968 RMVar_ID_81968 Human_SNP_ID_658913011 m1A Human chr19 + 12954507 12954507 12954507 GTTCACAATCATCTGTGGCATCTTGGCCATGCACTCTGCGATGTGCTGCTCCCTGCAGGGGAGGG GTTCACAATCATCTGTGGCATCTTGGCCATGCGCTCTGCGATGTGCTGCTCCCTGCAGGGGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12954270..12954573 26863196 MeRIP-seq:(Medium) rs776275022 Functional Loss SNV dbSNP153 33..33 33 - - - 81969 RMVar_ID_81969 Human_SNP_ID_658913732 m1A Human chr19 - 12956962 12956962 12956962 TTCGTTATGGCCGTCGCCGGAGCAGCTGCGGGAGCTGGAGGCCGAAGAACGCGAATGGTACCCGA TTCGTTATGGCCGTCGCCGGAGCAGCTGCGGGTGCTGGAGGCCGAAGAACGCGAATGGTACCCGA T A GADD45GIP1 Ensembl:ENSG00000179271 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12956951..12956975 26863196 MeRIP-seq:(Medium) rs767324749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138656,Human_RBP_ID_772195,Human_RBP_ID_1554936,Human_RBP_ID_4503332,Human_RBP_ID_8839148,Human_RBP_ID_9293431,Human_RBP_ID_9328671,Human_RBP_ID_22446504,Human_RBP_ID_26983200,Human_RBP_ID_27268225,Human_RBP_ID_27463744 Human_Splice_Rec_1964553 RMVar_hsa_circ_124765,RMVar_hsa_circ_192859 81970 RMVar_ID_81970 Human_SNP_ID_658925277 m1A Human chr19 + 12995576 12995567 12995576 GCGGCGGCGGCATGGAGTAGACGCGCGGCGGCAGCGGCGGCGGCGGCGGACGCGAGAGGCAGCGG GCGGCGGCGGCATGGAGTAGACGC_________GCGGCGGCGGCGGCGGACGCGAGAGGCAGCGG CGCGGCGGCA C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr19:12995565..12995697;chr19:12995502..12995680;chr19:12995458..12995972 26863196 MeRIP-seq:(Medium) rs1339941851 Functional Loss DEL dbSNP153 25..33 33 - - - 81971 RMVar_ID_81971 Human_SNP_ID_658925353 m1A Human chr19 - 12995782 12995782 12995782 CGGCGGCCGGCCGCGGCGAGGGGAGGCCCGGCAGGCGGCGGCCGCGCTCGGGCTCGGGCTCCGGC CGGCGGCCGGCCGCGGCGAGGGGAGGCCCGGCCGGCGGCGGCCGCGCTCGGGCTCGGGCTCCGGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:12995702..12995789 26863410 MeRIP-seq:(Medium) rs894170725 Functional Loss SNV dbSNP153 33..33 33 - - - 81972 RMVar_ID_81972 Human_SNP_ID_658931432 m1A Human chr19 - 13018357 13018357 13018357 TCACAGCCAGGCCGCACACTTCTCTCCTGTAAACCGCGCCCCCCCCCCCCCCCCGCCCCTTCCTT TCACAGCCAGGCCGCACACTTCTCTCCTGTAACCCGCGCCCCCCCCCCCCCCCCGCCCCTTCCTT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:13018326..13018375 26863196 MeRIP-seq:(Medium) rs1204357597 Functional Loss SNV dbSNP153 33..33 33 - - - 81973 RMVar_ID_81973 Human_SNP_ID_658932742 m1A Human chr19 - 13023404 13023404 13023404 GAAAAGGGGGAGCTCGCAGATTCCCGGGGAAGAGGACGAGTTCTGACCGGCTGCAGACCGTTGCT GAAAAGGGGGAGCTCGCAGATTCCCGGGGAAGTGGACGAGTTCTGACCGGCTGCAGACCGTTGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13023391..13023504 26863196 MeRIP-seq:(Medium) rs986813269 Functional Loss SNV dbSNP153 33..33 33 - - - 81974 RMVar_ID_81974 Human_SNP_ID_658946928 m1A Human chr19 + 13081758 13081758 13081758 CATCATCCAGCAGTCGAGCCCGTATTTCACGCACCCGACCATCCGCTACCACCACCACCACGGGC CATCATCCAGCAGTCGAGCCCGTATTTCACGCCCCCGACCATCCGCTACCACCACCACCACGGGC A C NFIX Ensembl:ENSG00000008441 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13081645..13081814 26863196 MeRIP-seq:(Medium) rs753831773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1964576,Human_Splice_Rec_1964577,Human_Splice_Rec_1964594,Human_Splice_Rec_1964595,Human_Splice_Rec_1964616,Human_Splice_Rec_1964630,Human_Splice_Rec_1964631,Human_Splice_Rec_1964648,Human_Splice_Rec_1964649,Human_Splice_Rec_1964666,Human_Splice_Rec_1964667,Human_Splice_Rec_1964682,Human_Splice_Rec_1964683,Human_Splice_Rec_1964700,Human_Splice_Rec_1964701,Human_Splice_Rec_1964720,Human_Splice_Rec_1964721,Human_Splice_Rec_1964742,Human_Splice_Rec_1964743 Human_miRNA_ID_1957694 RMVar_hsa_circ_8272,RMVar_hsa_circ_349077,RMVar_hsa_circ_29608,RMVar_hsa_circ_293148,RMVar_hsa_circ_192863,RMVar_hsa_circ_67651,RMVar_hsa_circ_335410 81975 RMVar_ID_81975 Human_SNP_ID_658948785 m1A Human chr19 + 13089004 13089004 13089004 GTGGGCCAGGGTGGGCAGCTCTGGGGGTGGGCAGGCCACAGGCCAGGGCAGTTCGGTGGCGGTGG GTGGGCCAGGGTGGGCAGCTCTGGGGGTGGGCCGGCCACAGGCCAGGGCAGTTCGGTGGCGGTGG A C NFIX Ensembl:ENSG00000008441 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:13089001..13089050 26863196 MeRIP-seq:(Medium) rs377020972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8272,RMVar_hsa_circ_29608,RMVar_hsa_circ_67651 81976 RMVar_ID_81976 Human_SNP_ID_658950263 m1A Human chr19 - 13094992 13094992 13094992 GTTGCTTTGTTTGGGGACTTTGTTCCTTCCCCAGAAGGCCGGGGCGGGGTCAGGGGGAGGAAGGC GTTGCTTTGTTTGGGGACTTTGTTCCTTCCCCGGAAGGCCGGGGCGGGGTCAGGGGGAGGAAGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13094943..13095273 26863196 MeRIP-seq:(Medium) rs1002788491 Functional Loss SNV dbSNP153 33..33 33 - - - 81977 RMVar_ID_81977 Human_SNP_ID_658950493 m1A Human chr19 + 13095688 13095688 13095688 AAAGGGGACCCCGGAGCCGAGCGAGGAGGACCAGGCAGCCGCCGCTGCCGCGCTAAGCCACCACC AAAGGGGACCCCGGAGCCGAGCGAGGAGGACCCGGCAGCCGCCGCTGCCGCGCTAAGCCACCACC A C NFIX Ensembl:ENSG00000008441 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13095653..13095802 26863196 MeRIP-seq:(Medium) rs1435157756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22593461 81978 RMVar_ID_81978 Human_SNP_ID_658953372 m1A Human chr19 - 13105002 13105002 13105002 GACACCCAGGGTTTCTGCTGATGCTGCCCCTGACTGTCCAGAGACCTCCAACCAGACCCCCCCTG GACACCCAGGGTTTCTGCTGATGCTGCCCCTGGCTGTCCAGAGACCTCCAACCAGACCCCCCCTG T C TRMT1 Ensembl:ENSG00000104907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13104951..13105107 26863196 MeRIP-seq:(Medium) rs1568354207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53042,Human_RBP_ID_9380629,Human_RBP_ID_13372729,Human_RBP_ID_22501699,Human_RBP_ID_23783171 Human_Splice_Rec_1964794,Human_Splice_Rec_1964826,Human_Splice_Rec_1964854,Human_Splice_Rec_1964884,Human_Splice_Rec_1964918,Human_Splice_Rec_1964946 RMVar_hsa_circ_125336,RMVar_hsa_circ_192868 81979 RMVar_ID_81979 Human_SNP_ID_658953557 m1A Human chr19 - 13105374 13105374 13105374 CCTCGCACAGGGGCAAGGCGGCCGACGAAGCTATGGAGGAGAGACGCAGGCTGCTTCAGAACAAG CCTCGCACAGGGGCAAGGCGGCCGACGAAGCTGTGGAGGAGAGACGCAGGCTGCTTCAGAACAAG T C TRMT1 Ensembl:ENSG00000104907 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13105243..13105441 26863196 MeRIP-seq:(Medium) rs1489613206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907406,Human_RBP_ID_1575217,Human_RBP_ID_3954560,Human_RBP_ID_5117701,Human_RBP_ID_5370050,Human_RBP_ID_9294266,Human_RBP_ID_18165989,Human_RBP_ID_18996820,Human_RBP_ID_19089415,Human_RBP_ID_22545691,Human_RBP_ID_24545580,Human_RBP_ID_26785363 Human_Splice_Rec_1964792,Human_Splice_Rec_1964824,Human_Splice_Rec_1964852,Human_Splice_Rec_1964916 RMVar_hsa_circ_125336,RMVar_hsa_circ_192868 81980 RMVar_ID_81980 Human_SNP_ID_658953568 m1A Human chr19 - 13105391 13105391 13105391 GTCCCACCTACTCCTCCCCTCGCACAGGGGCAAGGCGGCCGACGAAGCTATGGAGGAGAGACGCA GTCCCACCTACTCCTCCCCTCGCACAGGGGCATGGCGGCCGACGAAGCTATGGAGGAGAGACGCA T A TRMT1 Ensembl:ENSG00000104907 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13105340..13105458 26863196 MeRIP-seq:(Medium) rs1165974315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770575,Human_RBP_ID_907406,Human_RBP_ID_1575217,Human_RBP_ID_3956412,Human_RBP_ID_5117701,Human_RBP_ID_5370050,Human_RBP_ID_9294266,Human_RBP_ID_18165668,Human_RBP_ID_18421284,Human_RBP_ID_18994444,Human_RBP_ID_19089415,Human_RBP_ID_22358905,Human_RBP_ID_22545691,Human_RBP_ID_24545580,Human_RBP_ID_26335818,Human_RBP_ID_26785363 Human_Splice_Rec_1964792,Human_Splice_Rec_1964824,Human_Splice_Rec_1964852,Human_Splice_Rec_1964916 RMVar_hsa_circ_125336,RMVar_hsa_circ_192868 81981 RMVar_ID_81981 Human_SNP_ID_658956956 m1A Human chr19 + 13115735 13115735 13115735 TTTCCTCCTCTTGCTCTGACAAGTCCACGACCACTTTTTGCGTGTCCTTCTCTCCTGGAACCTTG TTTCCTCCTCTTGCTCTGACAAGTCCACGACCGCTTTTTGCGTGTCCTTCTCTCCTGGAACCTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13115605..13115776 26863196 MeRIP-seq:(Medium) rs776717339 Functional Loss SNV dbSNP153 33..33 33 - - - 81982 RMVar_ID_81982 Human_SNP_ID_658957082 m1A Human chr19 + 13116046 13116046 13116046 CCAAGCTGAATGCGAGCAAACTCGGTGATCACAGCACATCTGGTGGGAGACAGAGGACTAGCTCA CCAAGCTGAATGCGAGCAAACTCGGTGATCACTGCACATCTGGTGGGAGACAGAGGACTAGCTCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:13115976..13116075 32194978 MeRIP-seq:(Medium) rs774459989 Functional Loss SNV dbSNP153 33..33 33 - - - 81983 RMVar_ID_81983 Human_SNP_ID_658957254 m1A Human chr19 - 13116395 13116395 13116395 GGCGGGCGGAGGCGCCAGCGGATGTCTCATGCAAGGATCGTCTCTGTGGCTAAGCCTCACTTTCC GGCGGGCGGAGGCGCCAGCGGATGTCTCATGCTAGGATCGTCTCTGTGGCTAAGCCTCACTTTCC T A TRMT1 Ensembl:ENSG00000104907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13116274..13116427 26863196 MeRIP-seq:(Medium) rs763950252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554952,Human_RBP_ID_4503502,Human_RBP_ID_8477639 Human_Splice_Rec_1964796,Human_Splice_Rec_1964888,Human_Splice_Rec_1964920,Human_Splice_Rec_1964970,Human_Splice_Rec_1964996,Human_Splice_Rec_1965010,Human_Splice_Rec_1965016,Human_Splice_Rec_1965022,Human_Splice_Rec_1965030,Human_Splice_Rec_1965036,Human_Splice_Rec_1965040,Human_Splice_Rec_1965044 RMVar_hsa_circ_1139,RMVar_hsa_circ_17022,RMVar_hsa_circ_80649,RMVar_hsa_circ_192872 81984 RMVar_ID_81984 Human_SNP_ID_658957346 m1A Human chr19 - 13116680 13116677 13116681 GGTCCTAATTCGGGAAACGTGCACCTTGACTAATTCGGTTTTCTGTGGCTACGAGAGCAGGTGAG GGTCCTAATTCGGGAAACGTGCACCTTGACT____CGGTTTTCTGTGGCTACGAGAGCAGGTGAG GAATT G TRMT1 Ensembl:ENSG00000104907 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13116539..13116679 26863196 MeRIP-seq:(Medium) rs1474300128 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_304134,Human_RBP_ID_4558144,Human_RBP_ID_5468274,Human_RBP_ID_13372814,Human_RBP_ID_18440580,Human_RBP_ID_18722895 Human_Splice_Rec_1964795,Human_Splice_Rec_1964855,Human_Splice_Rec_1964887,Human_Splice_Rec_1964919,Human_Splice_Rec_1964955,Human_Splice_Rec_1964969,Human_Splice_Rec_1964995,Human_Splice_Rec_1965001,Human_Splice_Rec_1965009,Human_Splice_Rec_1965015,Human_Splice_Rec_1965021,Human_Splice_Rec_1965029,Human_Splice_Rec_1965035,Human_Splice_Rec_1965037,Human_Splice_Rec_1965039,Human_Splice_Rec_1965043 RMVar_hsa_circ_1139 81985 RMVar_ID_81985 Human_SNP_ID_658957715 m1A Human chr19 + 13118106 13118106 13118106 GAGCTGAGCCGACGTACTGGCGAGGATCCCCCAGGGGCATAGAGAGGAGACGGAGCCGGTTAGAA GAGCTGAGCCGACGTACTGGCGAGGATCCCCCGGGGGCATAGAGAGGAGACGGAGCCGGTTAGAA A G NACC1 Ensembl:ENSG00000160877 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13117983..13118105 26863196 MeRIP-seq:(Medium) rs1399363471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013212 Human_Splice_Rec_1965047 81986 RMVar_ID_81986 Human_SNP_ID_658958039 m1A Human chr19 + 13118980 13118980 13118980 GGGCGGCTGAGGAGAAGCCCAGGAAGTGGGGCACGGCGGGTGTGGGCGGAGTTACTTCGTGTGGG GGGCGGCTGAGGAGAAGCCCAGGAAGTGGGGCGCGGCGGGTGTGGGCGGAGTTACTTCGTGTGGG A G NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13118587..13119261 26863196 MeRIP-seq:(Medium) rs898539590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583247,Human_RBP_ID_8196148,Human_RBP_ID_9426009,Human_RBP_ID_22524385 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 81987 RMVar_ID_81987 Human_SNP_ID_658958040 m1A Human chr19 + 13118980 13118980 13118980 GGGCGGCTGAGGAGAAGCCCAGGAAGTGGGGCACGGCGGGTGTGGGCGGAGTTACTTCGTGTGGG GGGCGGCTGAGGAGAAGCCCAGGAAGTGGGGCTCGGCGGGTGTGGGCGGAGTTACTTCGTGTGGG A T NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13118587..13119261 26863196 MeRIP-seq:(Medium) rs898539590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583247,Human_RBP_ID_8196148,Human_RBP_ID_9426009,Human_RBP_ID_22524385 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 81988 RMVar_ID_81988 Human_SNP_ID_658958044 m1A Human chr19 + 13118997 13118997 13118997 CCCAGGAAGTGGGGCACGGCGGGTGTGGGCGGAGTTACTTCGTGTGGGGGCGGATAGGAGATCCC CCCAGGAAGTGGGGCACGGCGGGTGTGGGCGGTGTTACTTCGTGTGGGGGCGGATAGGAGATCCC A T NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13118876..13119140 26863196 MeRIP-seq:(Medium) rs1241252953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583247,Human_RBP_ID_8196148,Human_RBP_ID_9425213,Human_RBP_ID_13372815,Human_RBP_ID_18945108,Human_RBP_ID_26785366 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 81989 RMVar_ID_81989 Human_SNP_ID_658962701 m1A Human chr19 + 13136040 13136040 13136040 AAGCGCCTACACCAGCGACAGCCCTGGCTCCTACCACAATGAGGAGGACGAGGAGGAGGATGGTG AAGCGCCTACACCAGCGACAGCCCTGGCTCCTGCCACAATGAGGAGGACGAGGAGGAGGATGGTG A G NACC1 Ensembl:ENSG00000160877 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13135847..13138159 32194978 MeRIP-seq:(Medium) rs1304755987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17915487,Human_RBP_ID_22809329,Human_RBP_ID_26464798 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874,RMVar_hsa_circ_297753,RMVar_hsa_circ_346181,RMVar_hsa_circ_192875 81990 RMVar_ID_81990 Human_SNP_ID_658963618 m1A Human chr19 + 13138736 13138736 13138736 CCAGGGGAGGGGGCTGGCCTGGGGGTCTTGGGAAGGCCCCTCCCCAGGCCCTAGGCCACCTCGCG CCAGGGGAGGGGGCTGGCCTGGGGGTCTTGGGCAGGCCCCTCCCCAGGCCCTAGGCCACCTCGCG A C NACC1 Ensembl:ENSG00000160877 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:13138726..13138775 26863196 MeRIP-seq:(Medium) rs1038599801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6721668,Human_RBP_ID_17272602,Human_RBP_ID_22229849 Human_miRNA_ID_2368234,Human_miRNA_ID_2391187,Human_miRNA_ID_2592432,Human_miRNA_ID_3016017 RMVar_hsa_circ_100302,RMVar_hsa_circ_108843,RMVar_hsa_circ_192874,RMVar_hsa_circ_192876 81991 RMVar_ID_81991 Human_SNP_ID_658963865 m1A Human chr19 + 13139520 13139520 13139520 CTGAATGTGTGTGTGTGGGTGTGTATGTGTGGAGTGTGTGTGTGTGTTTCCATGGTAGGACTCCA CTGAATGTGTGTGTGTGGGTGTGTATGTGTGGTGTGTGTGTGTGTGTTTCCATGGTAGGACTCCA A T NACC1 Ensembl:ENSG00000160877 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13139424..13139620 26863196 MeRIP-seq:(Medium) rs914547388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067229,Human_RBP_ID_1093649,Human_RBP_ID_5116125,Human_RBP_ID_5145068,Human_RBP_ID_5292715,Human_RBP_ID_5649916,Human_RBP_ID_6721689,Human_RBP_ID_9329809,Human_RBP_ID_17272050,Human_RBP_ID_18461200,Human_RBP_ID_23783227,Human_RBP_ID_26472095 Human_miRNA_ID_1388691 RMVar_hsa_circ_100302,RMVar_hsa_circ_108843,RMVar_hsa_circ_192874,RMVar_hsa_circ_192876 81992 RMVar_ID_81992 Human_SNP_ID_658964279 m1A Human chr19 + 13140930 13140930 13140930 CTCCCCTGCCAACTCCCCTTCCCTGGCCGCCCACTCAACCCACACCTCTTTCACGCAGGACAGGC CTCCCCTGCCAACTCCCCTTCCCTGGCCGCCCCCTCAACCCACACCTCTTTCACGCAGGACAGGC A C NACC1 Ensembl:ENSG00000160877 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13140732..13140975 26863196 MeRIP-seq:(Medium) rs1475922448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3587946,Human_RBP_ID_5442692,Human_RBP_ID_8255805,Human_RBP_ID_17266748,Human_RBP_ID_17382150,Human_RBP_ID_17915534,Human_RBP_ID_18945118,Human_RBP_ID_21929739,Human_RBP_ID_22422219,Human_RBP_ID_23783255,Human_RBP_ID_27463822 RMVar_hsa_circ_100302,RMVar_hsa_circ_108843,RMVar_hsa_circ_192874,RMVar_hsa_circ_192876 81993 RMVar_ID_81993 Human_SNP_ID_658967139 m1A Human chr19 - 13149734 13149733 13149735 GCATCGAGTGGGACCTCGAGGACCTGGAAGAGACCATCGATATCCTGGGGCTTTGTGGCAGAGGG GCATCGAGTGGGACCTCGAGGACCTGGAAGA__CCATCGATATCCTGGGGCTTTGTGGCAGAGGG GTC G STX10 Ensembl:ENSG00000104915 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13149726..13149884 32194978 MeRIP-seq:(Medium) rs747299690 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5588307 Human_Splice_Rec_1965067 RMVar_hsa_circ_192882 81994 RMVar_ID_81994 Human_SNP_ID_658967140 m1A Human chr19 - 13149734 13149734 13149734 GCATCGAGTGGGACCTCGAGGACCTGGAAGAGACCATCGATATCCTGGGGCTTTGTGGCAGAGGG GCATCGAGTGGGACCTCGAGGACCTGGAAGAGGCCATCGATATCCTGGGGCTTTGTGGCAGAGGG T C STX10 Ensembl:ENSG00000104915 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13149726..13149884 32194978 MeRIP-seq:(Medium) rs778685856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5588307 Human_Splice_Rec_1965067 RMVar_hsa_circ_192882 81995 RMVar_ID_81995 Human_SNP_ID_658967155 m1A Human chr19 + 13149763 13149763 13149763 TGGTCTCTTCCAGGTCCTCGAGGTCCCACTCGATGCTGCGCAGGCCATTCCGCAGCTCATTGGTC TGGTCTCTTCCAGGTCCTCGAGGTCCCACTCGGTGCTGCGCAGGCCATTCCGCAGCTCATTGGTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:13149758..13149933 26863196 MeRIP-seq:(Medium) rs749847739 Functional Loss SNV dbSNP153 33..33 33 - - - 81996 RMVar_ID_81996 Human_SNP_ID_658967201 m1A Human chr19 - 13149844 13149844 13149844 CACGGCCCGCGGGCTGTACCAGCGCTGGTGCGAGCTCCTGCAGGAAAGCGCGGCGGTCGGACGCG CACGGCCCGCGGGCTGTACCAGCGCTGGTGCGGGCTCCTGCAGGAAAGCGCGGCGGTCGGACGCG T C STX10 Ensembl:ENSG00000104915 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr19:13149471..13150325;chr19:13149526..13149952 26863196 MeRIP-seq:(Medium) rs981552486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559292,Human_RBP_ID_5320192,Human_RBP_ID_23783281 Human_Splice_Rec_1965066,Human_Splice_Rec_1965076,Human_Splice_Rec_1965084,Human_Splice_Rec_1965106,Human_Splice_Rec_1965116,Human_Splice_Rec_1965136 81997 RMVar_ID_81997 Human_SNP_ID_658967331 m1A Human chr19 + 13150172 13150161 13150172 CTCGGACTACAAAAAAGGGGTCTTCGAGAGACATGTCAGTCCCTTCCCCCCCAGGCCGAACCCCC CTCGGACTACAAAAAAGGGGTC___________TGTCAGTCCCTTCCCCCCCAGGCCGAACCCCC CTTCGAGAGACA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:13150160..13150245 26863410 MeRIP-seq:(Medium) rs1568394830 Functional Loss DEL dbSNP153 23..33 33 - - - 81998 RMVar_ID_81998 Human_SNP_ID_658967523 m1A Human chr19 + 13150544 13150544 13150544 GTTCCTGCGCAACTTCAGTTTCCCTTCCAGGCACGGGCAATGTAAATAATGATAGCCTCCCTCAT GTTCCTGCGCAACTTCAGTTTCCCTTCCAGGCCCGGGCAATGTAAATAATGATAGCCTCCCTCAT A C IER2 Ensembl:ENSG00000160888 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13150497..13150632 26863196 MeRIP-seq:(Medium) rs559940993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558150,Human_RBP_ID_8233087,Human_RBP_ID_21892165 Human_Splice_Rec_1965161,Human_Splice_Rec_1965163 81999 RMVar_ID_81999 Human_SNP_ID_658967973 m1A Human chr19 + 13151946 13151946 13151946 AGTTGTGGAAGTCAGCGGGCGCTGGTGGCGGGAAGGCGCCGCGAGCCAGTGCGGGCGGAAAGGGG AGTTGTGGAAGTCAGCGGGCGCTGGTGGCGGGTAGGCGCCGCGAGCCAGTGCGGGCGGAAAGGGG A T IER2 Ensembl:ENSG00000160888 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13151901..13152026 26863196 MeRIP-seq:(Medium) rs936015202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3580907,Human_RBP_ID_4559300,Human_RBP_ID_5145680,Human_RBP_ID_5238678,Human_RBP_ID_8100400,Human_RBP_ID_18490321,Human_RBP_ID_22719103,Human_RBP_ID_23257726 82000 RMVar_ID_82000 Human_SNP_ID_658968321 m1A Human chr19 - 13153089 13153089 13153089 GGACAACGGGCTCGCTCACGCCTCTCTACACAAACCAACCCACGCAGTGACACTGCTAGGACGCT GGACAACGGGCTCGCTCACGCCTCTCTACACACACCAACCCACGCAGTGACACTGCTAGGACGCT T G AC011446.2 Ensembl:ENSG00000267598 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:13153076..13153225 26863196 MeRIP-seq:(Medium) rs544804758 Functional Loss SNV dbSNP153 33..33 33 - - - 82001 RMVar_ID_82001 Human_SNP_ID_658968654 m1A Human chr19 + 13153626 13153624 13153627 CCCGAGCAAGAAAGCCCGTCTGGAAGAAAAGGAAGAAGAGGAGGGAGCGTCATCCGAAGTCGCCG CCCGAGCAAGAAAGCCCGTCTGGAAGAAAAG___GAAGAGGAGGGAGCGTCATCCGAAGTCGCCG GGAA G IER2 Ensembl:ENSG00000160888 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:13153001..13154076;chr19:13153315..13153709 26863196 MeRIP-seq:(Medium) rs753469144 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_55453,Human_RBP_ID_4503864,Human_RBP_ID_26335829 82002 RMVar_ID_82002 Human_SNP_ID_658968821 m1A Human chr19 + 13153919 13153919 13153919 GAGCGCGCGTCGAACCGTCGGCCCGAGGGCGCAGACCTGAGGCGAGGCCACCCCCCTCCATCCTG GAGCGCGCGTCGAACCGTCGGCCCGAGGGCGCGGACCTGAGGCGAGGCCACCCCCCTCCATCCTG A G IER2 Ensembl:ENSG00000160888 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13153869..13153934 26863196 MeRIP-seq:(Medium) rs1025840425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4503877,Human_RBP_ID_26335831,Human_RBP_ID_27268339,Human_RBP_ID_27573161,Human_RBP_ID_27816165 Human_miRNA_ID_1009356 82003 RMVar_ID_82003 Human_SNP_ID_658985586 m1A Human chr19 - 13207072 13207072 13207072 GCGCCCCCCAACCAGCCCCGATCCCCCCACCCACGACAGGGGCTCTCGGGTGGGAGGCAGGGAGC GCGCCCCCCAACCAGCCCCGATCCCCCCACCCGCGACAGGGGCTCTCGGGTGGGAGGCAGGGAGC T C CACNA1A Ensembl:ENSG00000141837 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:13207065..13207203 26863196 MeRIP-seq:(Medium) rs892375497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266386 82004 RMVar_ID_82004 Human_SNP_ID_658994830 m1A Human chr19 - 13235652 13235652 13235652 GGCTCATCAAACTTCTCCGTCAGGGTTACACCATCCGCATTCTTCTCTGGACCTTTGTGCAGTCC GGCTCATCAAACTTCTCCGTCAGGGTTACACCGTCCGCATTCTTCTCTGGACCTTTGTGCAGTCC T C CACNA1A Ensembl:ENSG00000141837 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13235650..13235775 26863196 MeRIP-seq:(Medium) rs766623973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1965226,Human_Splice_Rec_1965227,Human_Splice_Rec_1965316,Human_Splice_Rec_1965317,Human_Splice_Rec_1965404,Human_Splice_Rec_1965405,Human_Splice_Rec_1965492,Human_Splice_Rec_1965493,Human_Splice_Rec_1965580,Human_Splice_Rec_1965581,Human_Splice_Rec_1965618,Human_Splice_Rec_1965619,Human_Splice_Rec_1965704,Human_Splice_Rec_1965705,Human_Splice_Rec_1965792,Human_Splice_Rec_1965793,Human_Splice_Rec_1965828,Human_Splice_Rec_1965829,Human_Splice_Rec_1965916,Human_Splice_Rec_1965917,Human_Splice_Rec_1966006,Human_Splice_Rec_1966007,Human_Splice_Rec_1966094,Human_Splice_Rec_1966095,Human_Splice_Rec_1966180,Human_Splice_Rec_1966181,Human_Splice_Rec_1966268,Human_Splice_Rec_1966269,Human_Splice_Rec_1966356,Human_Splice_Rec_1966357,Human_Splice_Rec_1966442,Human_Splice_Rec_1966443,Human_Splice_Rec_1966478,Human_Splice_Rec_1966479,Human_Splice_Rec_1966562,Human_Splice_Rec_1966563,Human_Splice_Rec_1966654,Human_Splice_Rec_1966655,Human_Splice_Rec_1966724,Human_Splice_Rec_1966725,Human_Splice_Rec_1966751,Human_Splice_Rec_1966766,Human_Splice_Rec_1966767,Human_Splice_Rec_1966778,Human_Splice_Rec_1966779,Human_Splice_Rec_1966802,Human_Splice_Rec_1966803,Human_Splice_Rec_1966814,Human_Splice_Rec_1966815,Human_Splice_Rec_1966830,Human_Splice_Rec_1966831,Human_Splice_Rec_1966846,Human_Splice_Rec_1966847,Human_Splice_Rec_1966856,Human_Splice_Rec_1966857,Human_Splice_Rec_1966863 RMVar_hsa_circ_100582,RMVar_hsa_circ_266386,RMVar_hsa_circ_266546,RMVar_hsa_circ_44628,RMVar_hsa_circ_265471,RMVar_hsa_circ_192883,RMVar_hsa_circ_269652,RMVar_hsa_circ_32517,RMVar_hsa_circ_17862,RMVar_hsa_circ_106634,RMVar_hsa_circ_329392,RMVar_hsa_circ_192886,RMVar_hsa_circ_341831,RMVar_hsa_circ_307625,RMVar_hsa_circ_192887 82005 RMVar_ID_82005 Human_SNP_ID_659132482 m1A Human chr19 - 13763022 13763022 13763022 AGTCGGAGTAGTCCGCCACGAGGGAGGAGCCGAGACTGCAGGGGTGCCGCGTGTCGGGGGTGTCA AGTCGGAGTAGTCCGCCACGAGGGAGGAGCCGGGACTGCAGGGGTGCCGCGTGTCGGGGGTGTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13762974..13763197 26863196 MeRIP-seq:(Medium) rs764748054 Functional Loss SNV dbSNP153 33..33 33 - - - 82006 RMVar_ID_82006 Human_SNP_ID_659132483 m1A Human chr19 - 13763022 13763022 13763022 AGTCGGAGTAGTCCGCCACGAGGGAGGAGCCGAGACTGCAGGGGTGCCGCGTGTCGGGGGTGTCA AGTCGGAGTAGTCCGCCACGAGGGAGGAGCCGCGACTGCAGGGGTGCCGCGTGTCGGGGGTGTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13762974..13763197 26863196 MeRIP-seq:(Medium) rs764748054 Functional Loss SNV dbSNP153 33..33 33 - - - 82007 RMVar_ID_82007 Human_SNP_ID_659132552 m1A Human chr19 + 13763131 13763129 13763131 CTAGAGGCCCGGACACACCCAGGAGGCCCCTCACAGACTGCAGACCCCCGGCTCGCCCACCAGCC CTAGAGGCCCGGACACACCCAGGAGGCCCCT__CAGACTGCAGACCCCCGGCTCGCCCACCAGCC TCA T CCDC130 Ensembl:ENSG00000104957 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:13762999..13763225 26863410 MeRIP-seq:(Medium) rs1008290560 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_27463901 RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 82008 RMVar_ID_82008 Human_SNP_ID_659133071 m1A Human chr19 + 13764589 13764589 13764589 CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCATGACCCTGGAGGCGATCCGCTACTCGCGGGGC CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCCTGACCCTGGAGGCGATCCGCTACTCGCGGGGC A C MRI1 Ensembl:ENSG00000037757 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13764526..13764741 26863196 MeRIP-seq:(Medium) rs765134239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513844,Human_RBP_ID_4558155,Human_RBP_ID_13374118,Human_RBP_ID_18420868 RMVar_hsa_circ_192921,RMVar_hsa_circ_88611 82009 RMVar_ID_82009 Human_SNP_ID_659133072 m1A Human chr19 + 13764589 13764589 13764589 CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCATGACCCTGGAGGCGATCCGCTACTCGCGGGGC CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCGTGACCCTGGAGGCGATCCGCTACTCGCGGGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13764526..13764741 26863196 MeRIP-seq:(Medium) rs765134239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513844,Human_RBP_ID_4558155,Human_RBP_ID_13374118,Human_RBP_ID_18420868 RMVar_hsa_circ_192921,RMVar_hsa_circ_88611 82010 RMVar_ID_82010 Human_SNP_ID_659133073 m1A Human chr19 + 13764589 13764589 13764589 CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCATGACCCTGGAGGCGATCCGCTACTCGCGGGGC CTCTGAGTTGCGCTGGGCTTGGCTGCTGCACCTTGACCCTGGAGGCGATCCGCTACTCGCGGGGC A T MRI1 Ensembl:ENSG00000037757 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13764526..13764741 26863196 MeRIP-seq:(Medium) rs765134239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513844,Human_RBP_ID_4558155,Human_RBP_ID_13374118,Human_RBP_ID_18420868 RMVar_hsa_circ_192921,RMVar_hsa_circ_88611 82011 RMVar_ID_82011 Human_SNP_ID_659133280 m1A Human chr19 - 13764995 13764995 13764995 CCATGTTGACAGCGGTGGGCCGGGCGGTGACGAGGAAGCTCAGCTTGTCGCGCACGAAGGCCACG CCATGTTGACAGCGGTGGGCCGGGCGGTGACGCGGAAGCTCAGCTTGTCGCGCACGAAGGCCACG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13764945..13765030 26863196 MeRIP-seq:(Medium) rs1431549391 Functional Loss SNV dbSNP153 33..33 33 - - - 82012 RMVar_ID_82012 Human_SNP_ID_659133570 m1A Human chr19 - 13765916 13765916 13765916 GTGACAAGGAGTTTTCAGCACCAGCCACCAGGACCCGGGGCCCAGGCCAACGCCTCCTCTCTGCC GTGACAAGGAGTTTTCAGCACCAGCCACCAGGCCCCGGGGCCCAGGCCAACGCCTCCTCTCTGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13765907..13766080 26863196 MeRIP-seq:(Medium) rs28420627 Functional Loss SNV dbSNP153 33..33 33 - - - 82013 RMVar_ID_82013 Human_SNP_ID_659133820 m1A Human chr19 + 13766573 13766573 13766573 AGGAGGAACTGGGGAGAAGGGAGTGAGCAGAGAAAGATTAGGTAGCTGTGACCAGGAGACAGGGG AGGAGGAACTGGGGAGAAGGGAGTGAGCAGAGGAAGATTAGGTAGCTGTGACCAGGAGACAGGGG A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13766534..13766624 26863196 MeRIP-seq:(Medium) rs915567846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374207 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431 82014 RMVar_ID_82014 Human_SNP_ID_659134509 m1A Human chr19 - 13768319 13768319 13768319 AAGGACACCTTCTCGGTGAAGCCTTCCCTGATATATCAGTTTTGCATAGCAATCCCCACACTTTC AAGGACACCTTCTCGGTGAAGCCTTCCCTGATGTATCAGTTTTGCATAGCAATCCCCACACTTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13768316..13768474 26863196 MeRIP-seq:(Medium) rs1404051690 Functional Loss SNV dbSNP153 33..33 33 - - - 82015 RMVar_ID_82015 Human_SNP_ID_659135884 m1A Human chr19 + 13772567 13772567 13772567 ATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ATGTGGATAACAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1376233591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1358389,Human_miRNA_ID_1694158,Human_miRNA_ID_2320072,Human_miRNA_ID_2326405,Human_miRNA_ID_2520781,Human_miRNA_ID_2523948,Human_miRNA_ID_2775777,Human_miRNA_ID_2836545,Human_miRNA_ID_2891200 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82016 RMVar_ID_82016 Human_SNP_ID_659135929 m1A Human chr19 + 13772734 13772734 13772734 CCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAAACTGGGAGGCAGAGCTT CCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATGGCGTGAAACTGGGAGGCAGAGCTT A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1142084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82017 RMVar_ID_82017 Human_SNP_ID_659136030 m1A Human chr19 + 13773078 13773078 13773078 TTACCCAGGCTGGAATGTAGAGGCGAGATCTCAGCTCACTGAAACCTGTGCCTCCCCGGTTCAAG TTACCCAGGCTGGAATGTAGAGGCGAGATCTCGGCTCACTGAAACCTGTGCCTCCCCGGTTCAAG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1293056844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374351,Human_RBP_ID_26464901 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82018 RMVar_ID_82018 Human_SNP_ID_659136068 m1A Human chr19 + 13773209 13773209 13773209 TTTTCTATTTTTAGTAGAGACATGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACTC TTTTCTATTTTTAGTAGAGACATGATTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACTC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1202714714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4504096,Human_RBP_ID_17568474 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82019 RMVar_ID_82019 Human_SNP_ID_659136110 m1A Human chr19 + 13773384 13773384 13773384 TGATGAGGCCAGGCTTGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGATCCCTTGAGCCC TGATGAGGCCAGGCTTGGTGGCTCATGCCTGTGATTCCAGCACTTTGGGAGGATCCCTTGAGCCC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1138206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4504099,Human_RBP_ID_17568475,Human_RBP_ID_26473608 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82020 RMVar_ID_82020 Human_SNP_ID_659136235 m1A Human chr19 + 13773855 13773855 13773855 AATTTTTGTATTTTTATTGGAGACACCATGTTAGTCGTGGCTGGTCTCCAACTCCTGACCTCGGG AATTTTTGTATTTTTATTGGAGACACCATGTTGGTCGTGGCTGGTCTCCAACTCCTGACCTCGGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1128029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013233,Human_RBP_ID_13374373,Human_RBP_ID_23174268,Human_RBP_ID_26472111,Human_RBP_ID_27674746 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82021 RMVar_ID_82021 Human_SNP_ID_659136257 m1A Human chr19 + 13773925 13773925 13773925 CGCGCCCCGCGGCCTCCGAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGCCCGGCCTAAATAA CGCGCCCCGCGGCCTCCGAAAGTGCTGGGATTGCAAGCGTGAGCCACCGTGCCCGGCCTAAATAA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1128033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 82022 RMVar_ID_82022 Human_SNP_ID_659137685 m1A Human chr19 - 13778087 13778087 13778087 GGCAGGCTGCTGCTGGCTTTCATCACCACGTCATGTTCGATCTTCTTCCGGATTCCGACTTCTAG GGCAGGCTGCTGCTGGCTTTCATCACCACGTCCTGTTCGATCTTCTTCCGGATTCCGACTTCTAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:13778051..13778425 32194978 MeRIP-seq:(Medium) rs150969669 Functional Loss SNV dbSNP153 33..33 33 - - - 82023 RMVar_ID_82023 Human_SNP_ID_659137719 m1A Human chr19 + 13778187 13778187 13778187 AGAAAGGGGCAGCTGCCGCCACCTCCTCCAAGACACCTTCCTGAGGACGCTGGCCCCAGTGCAGG AGAAAGGGGCAGCTGCCGCCACCTCCTCCAAGTCACCTTCCTGAGGACGCTGGCCCCAGTGCAGG A T C19orf53 Ensembl:ENSG00000104979 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13778003..13778475 26863196 MeRIP-seq:(Medium) rs774280923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55084,Human_RBP_ID_513875,Human_RBP_ID_9380650,Human_RBP_ID_17387243,Human_RBP_ID_17915607,Human_RBP_ID_26335840,Human_RBP_ID_26815387 Human_miRNA_ID_1192102,Human_miRNA_ID_1265237,Human_miRNA_ID_1270438,Human_miRNA_ID_1336862 82024 RMVar_ID_82024 Human_SNP_ID_659146250 m1A Human chr19 - 13806703 13806703 13806703 CACCCAACCACTCATCCTCACCTCCAATCACCACCAGTTCTGTCCTTCCCTTCTTTTTTTTTTTT CACCCAACCACTCATCCTCACCTCCAATCACCCCCAGTTCTGTCCTTCCCTTCTTTTTTTTTTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13806697..13806817 26863196 MeRIP-seq:(Medium) rs1022791426 Functional Loss SNV dbSNP153 33..33 33 - - - 82025 RMVar_ID_82025 Human_SNP_ID_659146293 m1A Human chr19 - 13806935 13806935 13806935 TCATATGTACCTCTCAAAACACCCACTACCCCATTCGTCCATCCATCCACCCTACACAAAGCGCC TCATATGTACCTCTCAAAACACCCACTACCCCTTTCGTCCATCCATCCACCCTACACAAAGCGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13806928..13806993 26863196 MeRIP-seq:(Medium) rs1429410084 Functional Loss SNV dbSNP153 33..33 33 - - - 82026 RMVar_ID_82026 Human_SNP_ID_659146424 m1A Human chr19 - 13807528 13807528 13807528 CACCAGGAGCTCATTCATCCATTTGTTCATTCATCCATTTACTTACCCATCCAATCCATTCATCT CACCAGGAGCTCATTCATCCATTTGTTCATTCTTCCATTTACTTACCCATCCAATCCATTCATCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13807179..13807806 26863196 MeRIP-seq:(Medium) rs1315244809 Functional Loss SNV dbSNP153 33..33 33 - - - 82027 RMVar_ID_82027 Human_SNP_ID_659148975 m1A Human chr19 + 13816052 13816049 13816053 GGGACAGAGAGAGATGGGGGGAGAGAGAGGGGAAGGAAGGAAGGGAGGGAGGGAAGGAGGCTGTA GGGACAGAGAGAGATGGGGGGAGAGAGAGG____GGAAGGAAGGGAGGGAGGGAAGGAGGCTGTA GGGAA G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13816048..13816298 26863196 MeRIP-seq:(Medium) rs1238286726 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_21621,RMVar_hsa_circ_53321,RMVar_hsa_circ_353580 82028 RMVar_ID_82028 Human_SNP_ID_659149424 m1A Human chr19 - 13817780 13817780 13817780 ACCTCCAGCGCCAGCACCAAGTAGGACTCCCCAGGGCTCCCGGGCACAGGCACGTGCTGGTAGGC ACCTCCAGCGCCAGCACCAAGTAGGACTCCCCGGGGCTCCCGGGCACAGGCACGTGCTGGTAGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:13817726..13817902 26863196 MeRIP-seq:(Medium) rs1441823850 Functional Loss SNV dbSNP153 33..33 33 - - - 82029 RMVar_ID_82029 Human_SNP_ID_659149464 m1A Human chr19 - 13817859 13817859 13817859 CTCCTCGTTGCGCACCACCTTGTCCTGGGCGTACAGCCCCTCCGGCAGGGCCCGCTGCTGCCCCA CTCCTCGTTGCGCACCACCTTGTCCTGGGCGTTCAGCCCCTCCGGCAGGGCCCGCTGCTGCCCCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13817813..13818017 26863196 MeRIP-seq:(Medium) rs1483191067 Functional Loss SNV dbSNP153 33..33 33 - - - 82030 RMVar_ID_82030 Human_SNP_ID_659151212 m1A Human chr19 + 13824067 13824063 13824067 AGAGAGGAAAGTGAGAGAGAGGAGGCTGGGAGAGAGAGAGAGGGAGAAAGGAGAGATAGTAGGGG AGAGAGGAAAGTGAGAGAGAGGAGGCTGG____GAGAGAGAGGGAGAAAGGAGAGATAGTAGGGG GGAGA G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13824056..13824161 26863196 MeRIP-seq:(Medium) rs146415972 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_353580,RMVar_hsa_circ_56786,RMVar_hsa_circ_345484,RMVar_hsa_circ_333666,RMVar_hsa_circ_45875,RMVar_hsa_circ_192935,RMVar_hsa_circ_192936,RMVar_hsa_circ_331535,RMVar_hsa_circ_192937 82031 RMVar_ID_82031 Human_SNP_ID_659151213 m1A Human chr19 + 13824067 13824063 13824067 AGAGAGGAAAGTGAGAGAGAGGAGGCTGGGAGAGAGAGAGAGGGAGAAAGGAGAGATAGTAGGGG AGAGAGGAAAGTGAGAGAGAGGAGGCTGGGA__GAGAGAGAGGGAGAAAGGAGAGATAGTAGGGG GGAGA GGA ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13824056..13824161 26863196 MeRIP-seq:(Medium) rs146415972 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_353580,RMVar_hsa_circ_56786,RMVar_hsa_circ_345484,RMVar_hsa_circ_333666,RMVar_hsa_circ_45875,RMVar_hsa_circ_192935,RMVar_hsa_circ_192936,RMVar_hsa_circ_331535,RMVar_hsa_circ_192937 82032 RMVar_ID_82032 Human_SNP_ID_659152288 m1A Human chr19 - 13827860 13827860 13827860 TCTTGCCTCTAAGTACCTGCTGTATAAGCCCCACCTTCACTAGGTCCCACCACCAATCAGCAGCT TCTTGCCTCTAAGTACCTGCTGTATAAGCCCCGCCTTCACTAGGTCCCACCACCAATCAGCAGCT T C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13827647..13827966 26863196 MeRIP-seq:(Medium) rs1254287373 Functional Loss SNV dbSNP153 33..33 33 - - - 82033 RMVar_ID_82033 Human_SNP_ID_659154959 m1A Human chr19 + 13836695 13836695 13836695 GCACAGGGGTGAGGGGGGCACCGGGCGGGGCCAGAGGCTGGCACCTGGAGGGGAGAAAGAGAGAG GCACAGGGGTGAGGGGGGCACCGGGCGGGGCCGGAGGCTGGCACCTGGAGGGGAGAAAGAGAGAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:13836651..13836783 26863196 MeRIP-seq:(Medium) rs1290284512 Functional Loss SNV dbSNP153 33..33 33 - - - 82034 RMVar_ID_82034 Human_SNP_ID_659155826 m1A Human chr19 - 13839569 13839569 13839569 CACATACATACCCTTGTGTGTCTGGTCCACGCACACGCTGTCTGGAGGGGGTATTCAGGCATACC CACATACATACCCTTGTGTGTCTGGTCCACGCGCACGCTGTCTGGAGGGGGTATTCAGGCATACC T C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:13839396..13839854;chr19:13839401..13839775 26863196 MeRIP-seq:(Medium) rs986029313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2556943 82035 RMVar_ID_82035 Human_SNP_ID_659156562 m1A Human chr19 - 13842010 13842009 13842010 CCCGTGCCTTTTGGCTGAAGGAGGAGGTTAAAAGGGCCCAGACTGAACCCCGACCCCTCTGTCTT CCCGTGCCTTTTGGCTGAAGGAGGAGGTTAAA_GGGCCCAGACTGAACCCCGACCCCTCTGTCTT CT C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr19:13841835..13842101;chr19:13841959..13842067 26863196,32194978 MeRIP-seq:(Medium) rs1238249773 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2556984 82036 RMVar_ID_82036 Human_SNP_ID_659156705 m1A Human chr19 - 13842514 13842514 13842514 GCGGCCGCGGAGTCCCGGGGCGCCCCCTACGGAGCGGGGGAAGGGCGGCCCGGCCTCTGTTCCCT GCGGCCGCGGAGTCCCGGGGCGCCCCCTACGGGGCGGGGGAAGGGCGGCCCGGCCTCTGTTCCCT T C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:13842326..13842925 26863196 MeRIP-seq:(Medium) rs1049525751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374764 82037 RMVar_ID_82037 Human_SNP_ID_659162118 m1A Human chr19 + 13860934 13860934 13860934 GCTGTGGTGGGGAGGGGATTAGGGGGATGGGGACAGACTGTCGGGGGCTGCAAGGTGTGCAGAGA GCTGTGGTGGGGAGGGGATTAGGGGGATGGGGTCAGACTGTCGGGGGCTGCAAGGTGTGCAGAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:13860897..13861081 26863196 MeRIP-seq:(Medium) rs571819166 Functional Loss SNV dbSNP153 33..33 33 - - - 82038 RMVar_ID_82038 Human_SNP_ID_659163337 m1A Human chr19 + 13865273 13865273 13865273 CGGCGGCGGCCACGGGTTCGAGCCGGCGCCGGAGCCCCGCGGCCCCCTCCCCCCCCCCGCCCACG CGGCGGCGGCCACGGGTTCGAGCCGGCGCCGGCGCCCCGCGGCCCCCTCCCCCCCCCCGCCCACG A C NANOS3 Ensembl:ENSG00000187556 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:13865253..13865338 26863410 MeRIP-seq:(Medium) rs1420478040 Functional Loss SNV dbSNP153 33..33 33 - - - 82039 RMVar_ID_82039 Human_SNP_ID_659165650 m1A Human chr19 + 13872803 13872803 13872803 GGATCTGCTGGACGTGGCGGATGAGCTGCGAGAGAGGGCGCCCCACTCCAGCTCCAGACAGAGGG GGATCTGCTGGACGTGGCGGATGAGCTGCGAGCGAGGGCGCCCCACTCCAGCTCCAGACAGAGGG A C NANOS3 Ensembl:ENSG00000187556 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13872798..13872869 26863196 MeRIP-seq:(Medium) rs1317607625 Functional Loss SNV dbSNP153 33..33 33 - - - 82040 RMVar_ID_82040 Human_SNP_ID_659165651 m1A Human chr19 + 13872803 13872803 13872803 GGATCTGCTGGACGTGGCGGATGAGCTGCGAGAGAGGGCGCCCCACTCCAGCTCCAGACAGAGGG GGATCTGCTGGACGTGGCGGATGAGCTGCGAGGGAGGGCGCCCCACTCCAGCTCCAGACAGAGGG A G NANOS3 Ensembl:ENSG00000187556 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13872798..13872869 26863196 MeRIP-seq:(Medium) rs1317607625 Functional Loss SNV dbSNP153 33..33 33 - - - 82041 RMVar_ID_82041 Human_SNP_ID_659171697 m1A Human chr19 - 13892158 13892158 13892158 AGGCAATTGGCCAGGTGCAGTGGCTCATGCCTATGATCCCAACACTTTGGGAGACTTCCCTTGAC AGGCAATTGGCCAGGTGCAGTGGCTCATGCCTGTGATCCCAACACTTTGGGAGACTTCCCTTGAC T C C19orf57 Ensembl:ENSG00000132016 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs542902089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31237 82042 RMVar_ID_82042 Human_SNP_ID_659175312 m1A Human chr19 + 13906315 13906315 13906315 CGGCCAAGCAGGGAAGCGAGGGCTCGGGATCGACGGCCGCGGGGCGCCGACGAGGAGTGCAGGAC CGGCCAAGCAGGGAAGCGAGGGCTCGGGATCGCCGGCCGCGGGGCGCCGACGAGGAGTGCAGGAC A C CC2D1A Ensembl:ENSG00000132024 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:13906201..13910011;chr19:13906201..13912612;chr19:13906198..13912574 26863196 MeRIP-seq:(Medium) rs1365386558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559301 82043 RMVar_ID_82043 Human_SNP_ID_659177201 m1A Human chr19 + 13913199 13913199 13913199 GCCGAAGCCTGAGGCCCCTCATCCGGGGCTGGAGACCACCTTGCAGGAGAGGCTGGCGCTCTATC GCCGAAGCCTGAGGCCCCTCATCCGGGGCTGGGGACCACCTTGCAGGAGAGGCTGGCGCTCTATC A G CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13906300..13913247 32194978 MeRIP-seq:(Medium) rs758622330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18996866 Human_Splice_Rec_1967356,Human_Splice_Rec_1967408,Human_Splice_Rec_1967430 RMVar_hsa_circ_5050,RMVar_hsa_circ_294116,RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955,RMVar_hsa_circ_308804,RMVar_hsa_circ_192941 82044 RMVar_ID_82044 Human_SNP_ID_659177360 m1A Human chr19 - 13913517 13913517 13913517 GACGCGATTCTAGGGGCCGGCTGGGTGGGTGCAGGGCTGTAGGTAGGCGTGGACGCCGGGCCTTT GACGCGATTCTAGGGGCCGGCTGGGTGGGTGCGGGGCTGTAGGTAGGCGTGGACGCCGGGCCTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13913472..13913649 26863196 MeRIP-seq:(Medium) rs753037271 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_424 82045 RMVar_ID_82045 Human_SNP_ID_659178696 m1A Human chr19 + 13918790 13918790 13918790 CAGACCCACCGTCACCACCGTCGCAGCCTCCGACCCCCGCTACGGCGCCCTCCACAACAGGTAGG CAGACCCACCGTCACCACCGTCGCAGCCTCCGCCCCCCGCTACGGCGCCCTCCACAACAGGTAGG A C CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:13918501..13919001;chr19:13918726..13918921 26863196 MeRIP-seq:(Medium) rs547816872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240337 Human_Splice_Rec_1967364,Human_Splice_Rec_1967365,Human_Splice_Rec_1967416,Human_Splice_Rec_1967417,Human_Splice_Rec_1967438,Human_Splice_Rec_1967439,Human_Splice_Rec_1967486,Human_Splice_Rec_1967487,Human_Splice_Rec_1967526,Human_Splice_Rec_1967527 RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 82046 RMVar_ID_82046 Human_SNP_ID_659178804 m1A Human chr19 + 13919041 13919041 13919041 GCGGAAAGCTCGAATGCACGAGCGCATCGTCAAGGTGCCCTGGGGGTTCCGGGGGAGGTGGGGCG GCGGAAAGCTCGAATGCACGAGCGCATCGTCAGGGTGCCCTGGGGGTTCCGGGGGAGGTGGGGCG A G CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13918999..13919977 32194978 MeRIP-seq:(Medium) rs996720493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19092451 Human_Splice_Rec_1967367,Human_Splice_Rec_1967419,Human_Splice_Rec_1967441,Human_Splice_Rec_1967489,Human_Splice_Rec_1967529 RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 82047 RMVar_ID_82047 Human_SNP_ID_659179327 m1A Human chr19 - 13920617 13920617 13920617 GGGGGGCGCTTTGGCTGTTGGGGCTGATCCCGACTGGGGAGTTCTTGAGGGTGGGGCTTTGGGCT GGGGGGCGCTTTGGCTGTTGGGGCTGATCCCGGCTGGGGAGTTCTTGAGGGTGGGGCTTTGGGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13920570..13920827 26863196 MeRIP-seq:(Medium) rs1157832326 Functional Loss SNV dbSNP153 33..33 33 - - - 82048 RMVar_ID_82048 Human_SNP_ID_659179336 m1A Human chr19 + 13920640 13920640 13920640 ACTCCCCAGTCGGGATCAGCCCCAACAGCCAAAGCGCCCCCCAAAGCCACATCCACCAGAGGTAA ACTCCCCAGTCGGGATCAGCCCCAACAGCCAACGCGCCCCCCAAAGCCACATCCACCAGAGGTAA A C CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13920510..13920704 26863196 MeRIP-seq:(Medium) rs878972868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18723013 Human_Splice_Rec_1967372,Human_Splice_Rec_1967373,Human_Splice_Rec_1967446,Human_Splice_Rec_1967447,Human_Splice_Rec_1967492,Human_Splice_Rec_1967493,Human_Splice_Rec_1967534,Human_Splice_Rec_1967535,Human_Splice_Rec_1967558,Human_Splice_Rec_1967559,Human_Splice_Rec_1967563 RMVar_hsa_circ_107714,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955,RMVar_hsa_circ_101859,RMVar_hsa_circ_309082,RMVar_hsa_circ_192943,RMVar_hsa_circ_298286,RMVar_hsa_circ_192945,RMVar_hsa_circ_192946,RMVar_hsa_circ_192944 82049 RMVar_ID_82049 Human_SNP_ID_659182129 m1A Human chr19 + 13929423 13929423 13929423 CCTGCATAGCCTCAGTGTGCTGGCGTTTGACCAAGAGCGTCTGGAGCGGAAGGTGGGTATCCATC CCTGCATAGCCTCAGTGTGCTGGCGTTTGACCCAGAGCGTCTGGAGCGGAAGGTGGGTATCCATC A C CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13927843..13930108 26863196 MeRIP-seq:(Medium) rs1312850121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240344,Human_RBP_ID_5585399 Human_Splice_Rec_1967396,Human_Splice_Rec_1967397,Human_Splice_Rec_1967470,Human_Splice_Rec_1967471,Human_Splice_Rec_1967516,Human_Splice_Rec_1967517,Human_Splice_Rec_1967554,Human_Splice_Rec_1967555,Human_Splice_Rec_1967590,Human_Splice_Rec_1967591 Human_miRNA_ID_1604447,Human_miRNA_ID_1678697 RMVar_hsa_circ_101859,RMVar_hsa_circ_192946 82050 RMVar_ID_82050 Human_SNP_ID_659182186 m1A Human chr19 - 13929565 13929565 13929565 TGTCCTGGTACTGCTGGGCCACTTCTGGGGGCACCGGCCGCCGCGCCTGCCTGAGGGCCAGGATC TGTCCTGGTACTGCTGGGCCACTTCTGGGGGCGCCGGCCGCCGCGCCTGCCTGAGGGCCAGGATC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:13929347..13929600 26863410 MeRIP-seq:(Medium) rs771776207 Functional Loss SNV dbSNP153 33..33 33 - - - 82051 RMVar_ID_82051 Human_SNP_ID_659182635 m1A Human chr19 - 13930725 13930725 13930725 GGGCTTTGGGGTTAAGGCTGGGGAGGAACAGGAAGTAAAGTGCTTGCAGGGGCCCTCGGGGCTTG GGGCTTTGGGGTTAAGGCTGGGGAGGAACAGGCAGTAAAGTGCTTGCAGGGGCCCTCGGGGCTTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13930675..13930830 26863196 MeRIP-seq:(Medium) rs1162782488 Functional Loss SNV dbSNP153 33..33 33 - - - 82052 RMVar_ID_82052 Human_SNP_ID_659189011 m1A Human chr19 + 13952535 13952535 13952535 GGGGGTGAAAATGGCGCCCAGCTCGAAATCGGAGCGGAACAGCGGGGCTGGGAGCGGCGGCGGCG GGGGGTGAAAATGGCGCCCAGCTCGAAATCGGCGCGGAACAGCGGGGCTGGGAGCGGCGGCGGCG A C DCAF15 Ensembl:ENSG00000132017 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:13952476..13952705;chr19:13952476..13952717;chr19:13952476..13952687 26863196 MeRIP-seq:(Medium) rs1396443327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9426022 RMVar_hsa_circ_121398,RMVar_hsa_circ_192953 82053 RMVar_ID_82053 Human_SNP_ID_659189012 m1A Human chr19 + 13952535 13952535 13952535 GGGGGTGAAAATGGCGCCCAGCTCGAAATCGGAGCGGAACAGCGGGGCTGGGAGCGGCGGCGGCG GGGGGTGAAAATGGCGCCCAGCTCGAAATCGGTGCGGAACAGCGGGGCTGGGAGCGGCGGCGGCG A T DCAF15 Ensembl:ENSG00000132017 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:13952476..13952705;chr19:13952476..13952717;chr19:13952476..13952687 26863196 MeRIP-seq:(Medium) rs1396443327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9426022 RMVar_hsa_circ_121398,RMVar_hsa_circ_192953 82054 RMVar_ID_82054 Human_SNP_ID_659189020 m1A Human chr19 + 13952543 13952543 13952543 AAATGGCGCCCAGCTCGAAATCGGAGCGGAACAGCGGGGCTGGGAGCGGCGGCGGCGGCCCCGGG AAATGGCGCCCAGCTCGAAATCGGAGCGGAACCGCGGGGCTGGGAGCGGCGGCGGCGGCCCCGGG A C DCAF15 Ensembl:ENSG00000132017 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:13952510..13952600 26863410 MeRIP-seq:(Medium) rs1568446921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_826044,Human_RBP_ID_9426022 RMVar_hsa_circ_121398,RMVar_hsa_circ_192953 82055 RMVar_ID_82055 Human_SNP_ID_659189583 m1A Human chr19 + 13954302 13954302 13954302 TCTCTGCCGTGGGTGAGGGGGCTGGGGGCTGCAGATGGTGCCTGAAGTGCCCTGGCCACCCCTTC TCTCTGCCGTGGGTGAGGGGGCTGGGGGCTGCGGATGGTGCCTGAAGTGCCCTGGCCACCCCTTC A G DCAF15 Ensembl:ENSG00000132017 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13954298..13954425 26863196 MeRIP-seq:(Medium) rs1353466540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22664975 RMVar_hsa_circ_121398,RMVar_hsa_circ_192953 82056 RMVar_ID_82056 Human_SNP_ID_659191769 m1A Human chr19 - 13960524 13960524 13960524 TCCTGTTGACGTAGCGGCCGCTGCTCTCCGGCACCAGCCACTTCATGACCATGTCCACGCAGCTC TCCTGTTGACGTAGCGGCCGCTGCTCTCCGGCCCCAGCCACTTCATGACCATGTCCACGCAGCTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13960476..13960575 32194978 MeRIP-seq:(Medium) rs202218518 Functional Loss SNV dbSNP153 33..33 33 - - - 82057 RMVar_ID_82057 Human_SNP_ID_659192314 m1A Human chr19 - 13961886 13961886 13961886 TCTCCTCCGTGCCGTGCGACCCCCACCCCATGACTATTGTGCGATTCGTGAGCGCCGCCCGAGCG TCTCCTCCGTGCCGTGCGACCCCCACCCCATGTCTATTGTGCGATTCGTGAGCGCCGCCCGAGCG T A RFX1 Ensembl:ENSG00000132005 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13961835..13962084 32194978 MeRIP-seq:(Medium) rs755065815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116742,Human_RBP_ID_18301620,Human_RBP_ID_18723035,Human_RBP_ID_23783472,Human_RBP_ID_27463971 82058 RMVar_ID_82058 Human_SNP_ID_659192916 m1A Human chr19 + 13963249 13963249 13963249 GGTGGAAGGAACCGAAGCTGGCGGCGCTGCGCAGGGTCAGGTCCCGGATCACCATGGAGCTGGGG GGTGGAAGGAACCGAAGCTGGCGGCGCTGCGCGGGGTCAGGTCCCGGATCACCATGGAGCTGGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13963007..13963551 32194978 MeRIP-seq:(Medium) rs1275131556 Functional Loss SNV dbSNP153 33..33 33 - - - 82059 RMVar_ID_82059 Human_SNP_ID_659195837 m1A Human chr19 + 13972896 13972893 13972896 CCCCCGCCACCGCCTCCCCCGCCGCCGCCGCCACCACCACTGCCACCACCTCCGCTGCTGTTGCT CCCCCGCCACCGCCTCCCCCGCCGCCGCCG___CCACCACTGCCACCACCTCCGCTGCTGTTGCT GCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13972859..13972980 26863196 MeRIP-seq:(Medium) rs756315571 Functional Loss DEL dbSNP153 31..33 33 - - - 82060 RMVar_ID_82060 Human_SNP_ID_659195839 m1A Human chr19 + 13972896 13972896 13972896 CCCCCGCCACCGCCTCCCCCGCCGCCGCCGCCACCACCACTGCCACCACCTCCGCTGCTGTTGCT CCCCCGCCACCGCCTCCCCCGCCGCCGCCGCCGCCACCACTGCCACCACCTCCGCTGCTGTTGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13972859..13972980 26863196 MeRIP-seq:(Medium) rs766666783 Functional Loss SNV dbSNP153 33..33 33 - - - 82061 RMVar_ID_82061 Human_SNP_ID_659204900 m1A Human chr19 - 14006210 14006210 14006210 CAACAACAACCGCCCGGCCGACCCCCACCCCCACCCCCCAGGCCCGGCCCGGGGACCCCAGCACG CAACAACAACCGCCCGGCCGACCCCCACCCCCCCCCCCCAGGCCCGGCCCGGGGACCCCAGCACG T G RFX1 Ensembl:ENSG00000132005 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14006159..14006299 26863196 MeRIP-seq:(Medium) rs1451871288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4504476 82062 RMVar_ID_82062 Human_SNP_ID_659212343 m1A Human chr19 + 14031812 14031812 14031812 GCCTCGGGCGCTGTACCCAGAGCTCGAAGAGGAGCAGCGCGGCCGCGCGGACCCGGCAAGGCTGG GCCTCGGGCGCTGTACCCAGAGCTCGAAGAGGGGCAGCGCGGCCGCGCGGACCCGGCAAGGCTGG A G IL27RA Ensembl:ENSG00000104998 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14031718..14031945 26863196 MeRIP-seq:(Medium) rs1006653335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557271 RMVar_hsa_circ_97630,RMVar_hsa_circ_192959 82063 RMVar_ID_82063 Human_SNP_ID_659212366 m1A Human chr19 - 14031852 14031852 14031852 GCCTCCCCGCATGGCGTCCCTCGGGAGCCCCGAGTCCGGCCCAGCCTTGCCGGGTCCGCGCGGCC GCCTCCCCGCATGGCGTCCCTCGGGAGCCCCGGGTCCGGCCCAGCCTTGCCGGGTCCGCGCGGCC T C RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14031819..14031970 26863196 MeRIP-seq:(Medium) rs1254468465 Functional Loss SNV dbSNP153 33..33 33 - - - 82064 RMVar_ID_82064 Human_SNP_ID_659212367 m1A Human chr19 - 14031852 14031852 14031852 GCCTCCCCGCATGGCGTCCCTCGGGAGCCCCGAGTCCGGCCCAGCCTTGCCGGGTCCGCGCGGCC GCCTCCCCGCATGGCGTCCCTCGGGAGCCCCGCGTCCGGCCCAGCCTTGCCGGGTCCGCGCGGCC T G RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14031819..14031970 26863196 MeRIP-seq:(Medium) rs1254468465 Functional Loss SNV dbSNP153 33..33 33 - - - 82065 RMVar_ID_82065 Human_SNP_ID_659219180 m1A Human chr19 - 14054239 14054239 14054239 ACCACTGGGCATAGAGAGAAAAGTTGAGGGACATTTGAGGGCAGAGAAGGAAGGAGATGAGGAAA ACCACTGGGCATAGAGAGAAAAGTTGAGGGACGTTTGAGGGCAGAGAAGGAAGGAGATGAGGAAA T C PALM3 Ensembl:ENSG00000187867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14054190..14054270 26863196 MeRIP-seq:(Medium) rs1309965286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192969,RMVar_hsa_circ_86826 82066 RMVar_ID_82066 Human_SNP_ID_659225418 m1A Human chr19 - 14074726 14074726 14074726 TTACTTCCGGCCGGGGGTCCCAGCCTTTTCAAACCTCAAGGTTTGCGCTCCTCCTGGGGACAGAG TTACTTCCGGCCGGGGGTCCCAGCCTTTTCAATCCTCAAGGTTTGCGCTCCTCCTGGGGACAGAG T A RF00017-124 RNACentral:URS000099C5B7 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14074326..14074866 32194978 MeRIP-seq:(Medium) rs766227363 Functional Loss SNV dbSNP153 33..33 33 - - - 82067 RMVar_ID_82067 Human_SNP_ID_659229559 m1A Human chr19 - 14088355 14088355 14088355 TTCCGGCCCCCATCTCACCCAAGATCCCCCAGAGTCCAGGAGCTGGACGGGGACACCCTCAGCCC TTCCGGCCCCCATCTCACCCAAGATCCCCCAGGGTCCAGGAGCTGGACGGGGACACCCTCAGCCC T C SAMD1 Ensembl:ENSG00000141858 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:14088305..14088463;chr19:14088304..14088420 26863196 MeRIP-seq:(Medium) rs1322248912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514005,Human_RBP_ID_4504656,Human_RBP_ID_17083822,Human_RBP_ID_17387249,Human_RBP_ID_18945130,Human_RBP_ID_23783616,Human_RBP_ID_26335859,Human_RBP_ID_27815212 Human_miRNA_ID_935837,Human_miRNA_ID_955815,Human_miRNA_ID_1148252,Human_miRNA_ID_1150306,Human_miRNA_ID_1151663,Human_miRNA_ID_1153004,Human_miRNA_ID_1154298,Human_miRNA_ID_1155590,Human_miRNA_ID_1160846,Human_miRNA_ID_1162159,Human_miRNA_ID_1228401 82068 RMVar_ID_82068 Human_SNP_ID_659229622 m1A Human chr19 - 14088459 14088459 14088459 ATCTACGAGCACCACATCAAGGTGCTTCAGCAAGGCCACTTTGAGGATGATGACCCCGATGGCTT ATCTACGAGCACCACATCAAGGTGCTTCAGCAGGGCCACTTTGAGGATGATGACCCCGATGGCTT T C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14087876..14089922 32194978 MeRIP-seq:(Medium) rs1240929011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514010,Human_RBP_ID_1555216,Human_RBP_ID_1880406,Human_RBP_ID_4562563,Human_RBP_ID_8477953 82069 RMVar_ID_82069 Human_SNP_ID_659230046 m1A Human chr19 + 14089170 14089170 14089170 CCGCCCTTCATCCTGGCCCTGGTGCGGTCCGCAGGGGGTCCACTCCTTGACCCTCTCCTTGGCAC CCGCCCTTCATCCTGGCCCTGGTGCGGTCCGCGGGGGGTCCACTCCTTGACCCTCTCCTTGGCAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14089054..14089275 26863196 MeRIP-seq:(Medium) rs1407368973 Functional Loss SNV dbSNP153 33..33 33 - - - 82070 RMVar_ID_82070 Human_SNP_ID_659230164 m1A Human chr19 - 14089330 14089330 14089330 AGAGGTGGAGAAGAGCGAGTACTTGAGAAAGAAGAGGAAGAAGATGATGATGAAGATGAAGATGA AGAGGTGGAGAAGAGCGAGTACTTGAGAAAGAGGAGGAAGAAGATGATGATGAAGATGAAGATGA T C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14089070..14089375 26863196 MeRIP-seq:(Medium) rs1033035869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54189,Human_RBP_ID_204500,Human_RBP_ID_514021,Human_RBP_ID_910785,Human_RBP_ID_1575219,Human_RBP_ID_1880408,Human_RBP_ID_2557125,Human_RBP_ID_6722176,Human_RBP_ID_18532275,Human_RBP_ID_23114720,Human_RBP_ID_24545581,Human_RBP_ID_26335860,Human_RBP_ID_27815214 Human_Splice_Rec_1967950,Human_Splice_Rec_1967958 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82071 RMVar_ID_82071 Human_SNP_ID_659230182 m1A Human chr19 - 14089360 14089360 14089360 AATTTTGCATGCTTCTCTCCTCGGCTCCAGAGAGGTGGAGAAGAGCGAGTACTTGAGAAAGAAGA AATTTTGCATGCTTCTCTCCTCGGCTCCAGAGGGGTGGAGAAGAGCGAGTACTTGAGAAAGAAGA T C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14089326..14089375 26863196 MeRIP-seq:(Medium) rs1295055896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575219,Human_RBP_ID_23114720,Human_RBP_ID_24545581 Human_Splice_Rec_1967950,Human_Splice_Rec_1967958 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82072 RMVar_ID_82072 Human_SNP_ID_659230748 m1A Human chr19 - 14090188 14090188 14090188 GCGCACGCGCGCCGAGCTCGAGAAACTGATCCAGCAGCGCGCCGTGCTCCGGGTCAGCTACAAGG GCGCACGCGCGCCGAGCTCGAGAAACTGATCCGGCAGCGCGCCGTGCTCCGGGTCAGCTACAAGG T C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14090151..14090225 26863196 MeRIP-seq:(Medium) rs868566770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6722178 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82073 RMVar_ID_82073 Human_SNP_ID_659230814 m1A Human chr19 - 14090372 14090342 14090372 CCCTACCCCCGCCGGAGACGGCGGCGGCCGCCACCACGGCGGCCGCCGCCTCGTCGTCCGCCGCT CCCTACCCCCGCCGGAGACGGCGGCGGCCGCC______________________________GCT CGGCGGACGACGAGGCGGCGGCCGCCGTGGT C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:14090276..14090525 26863410 MeRIP-seq:(Medium) rs1049078216 Functional Loss DEL dbSNP153 33..62 33 - - - Human_RBP_ID_4504724,Human_RBP_ID_5321475,Human_RBP_ID_9329829,Human_RBP_ID_22593484 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82074 RMVar_ID_82074 Human_SNP_ID_659230832 m1A Human chr19 - 14090372 14090357 14090372 CCCTACCCCCGCCGGAGACGGCGGCGGCCGCCACCACGGCGGCCGCCGCCTCGTCGTCCGCCGCT CCCTACCCCCGCCGGAGACGGCGGCGGCCGCC_______________GCCTCGTCGTCCGCCGCT CGGCGGCCGCCGTGGT C SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:14090276..14090525 26863410 MeRIP-seq:(Medium) rs753443431 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_4504724,Human_RBP_ID_5321475,Human_RBP_ID_9329829,Human_RBP_ID_22593484 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82075 RMVar_ID_82075 Human_SNP_ID_659230848 m1A Human chr19 - 14090372 14090372 14090372 CCCTACCCCCGCCGGAGACGGCGGCGGCCGCCACCACGGCGGCCGCCGCCTCGTCGTCCGCCGCT CCCTACCCCCGCCGGAGACGGCGGCGGCCGCCCCCACGGCGGCCGCCGCCTCGTCGTCCGCCGCT T G SAMD1 Ensembl:ENSG00000141858 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:14090276..14090525 26863410 MeRIP-seq:(Medium) rs987964190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4504724,Human_RBP_ID_5321475,Human_RBP_ID_9329829,Human_RBP_ID_22593484 RMVar_hsa_circ_192970,RMVar_hsa_circ_91435 82076 RMVar_ID_82076 Human_SNP_ID_659230865 m1A Human chr19 + 14090401 14090401 14090401 TGGTGGCGGCCGCCGCCGTCTCCGGCGGGGGTAGGGCCGGGGGCCCCGCCATGCCTCCCGCCCGG TGGTGGCGGCCGCCGCCGTCTCCGGCGGGGGTGGGGCCGGGGGCCCCGCCATGCCTCCCGCCCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14090301..14090450 26863410 MeRIP-seq:(Medium) rs1039626668 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 82077 RMVar_ID_82077 Human_SNP_ID_659230881 m1A Human chr19 - 14090440 14090440 14090440 CCGCGCTGGGAGGGAGGCAGCGCGCACGGTGCAGCCGGGCCGGGCGGGAGGCATGGCGGGGCCCC CCGCGCTGGGAGGGAGGCAGCGCGCACGGTGCTGCCGGGCCGGGCGGGAGGCATGGCGGGGCCCC T A SAMD1 Ensembl:ENSG00000141858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14090126..14090575 26863196 MeRIP-seq:(Medium) rs1319310323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557273,Human_RBP_ID_5320211,Human_RBP_ID_8233093,Human_RBP_ID_9328703,Human_RBP_ID_17670282,Human_RBP_ID_20433266,Human_RBP_ID_21977736,Human_RBP_ID_22533123 82078 RMVar_ID_82078 Human_SNP_ID_659231710 m1A Human chr19 - 14091999 14091999 14091999 GTTTTACTCACCCACCAGCTTCCGCCTCCCCCATCCTGGGCGCCCCTCCTCCAGCTTAGCTGTCA GTTTTACTCACCCACCAGCTTCCGCCTCCCCCTTCCTGGGCGCCCCTCCTCCAGCTTAGCTGTCA T A PRKACA Ensembl:ENSG00000072062 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14091951..14092131 26863196 MeRIP-seq:(Medium) rs781626359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241099,Human_RBP_ID_514030,Human_RBP_ID_4562584,Human_RBP_ID_5131057,Human_RBP_ID_23783629 82079 RMVar_ID_82079 Human_SNP_ID_659231989 m1A Human chr19 + 14092898 14092898 14092898 GGAAAGAGGAAGGGAAAAGTGGGAGAGGGGGCAGGAGGGTGAAGGGGATGAGGGGGAGCAGCTGG GGAAAGAGGAAGGGAAAAGTGGGAGAGGGGGCTGGAGGGTGAAGGGGATGAGGGGGAGCAGCTGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14092848..14092994 26863196 MeRIP-seq:(Medium) rs1027458185 Functional Loss SNV dbSNP153 33..33 33 - - - 82080 RMVar_ID_82080 Human_SNP_ID_659235919 m1A Human chr19 + 14106865 14106865 14106865 AAGGAGCCCGTGCCGAGGGTCTTGATTCGTTCAAACTGATCCAAGTGGGCTGTGTTCTGTGGGCA AAGGAGCCCGTGCCGAGGGTCTTGATTCGTTCTAACTGATCCAAGTGGGCTGTGTTCTGTGGGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14106815..14106927 26863196 MeRIP-seq:(Medium) rs1348252622 Functional Loss SNV dbSNP153 33..33 33 - - - 82081 RMVar_ID_82081 Human_SNP_ID_659235921 m1A Human chr19 + 14106876 14106876 14106876 GCCGAGGGTCTTGATTCGTTCAAACTGATCCAAGTGGGCTGTGTTCTGTGGGCAGAGGGGTCGGT GCCGAGGGTCTTGATTCGTTCAAACTGATCCACGTGGGCTGTGTTCTGTGGGCAGAGGGGTCGGT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14106826..14106900 26863196 MeRIP-seq:(Medium) rs56029020 Functional Loss SNV dbSNP153 33..33 33 - - - 82082 RMVar_ID_82082 Human_SNP_ID_659235926 m1A Human chr19 - 14106887 14106887 14106887 GCCCTGAGCCTACCGACCCCTCTGCCCACAGAACACAGCCCACTTGGATCAGTTTGAACGAATCA GCCCTGAGCCTACCGACCCCTCTGCCCACAGACCACAGCCCACTTGGATCAGTTTGAACGAATCA T G PRKACA Ensembl:ENSG00000072062 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14106851..14106944 26863196 MeRIP-seq:(Medium) rs1325870574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913811,Human_RBP_ID_27268622 Human_Splice_Rec_1967970,Human_Splice_Rec_1967988,Human_Splice_Rec_1968022,Human_Splice_Rec_1968048,Human_Splice_Rec_1968060,Human_Splice_Rec_1968072 RMVar_hsa_circ_350951,RMVar_hsa_circ_192972,RMVar_hsa_circ_192971,RMVar_hsa_circ_278805,RMVar_hsa_circ_119093,RMVar_hsa_circ_291481,RMVar_hsa_circ_192974 82083 RMVar_ID_82083 Human_SNP_ID_659241210 m1A Human chr19 - 14126239 14126239 14126239 ATTTCAATTAGTTAACCCTCCTATATCTTTGCAGACCTGGAGTGGAAGATCATTTATGTTGGCTC ATTTCAATTAGTTAACCCTCCTATATCTTTGCGGACCTGGAGTGGAAGATCATTTATGTTGGCTC T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14126208..14126288 26863196 MeRIP-seq:(Medium) rs1165713169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_910787 82084 RMVar_ID_82084 Human_SNP_ID_659244212 m1A Human chr19 + 14136446 14136446 14136446 GGTTCTCCAGGACCGCCACGTTCAGCACCGACACCTTGGCCATCGCCTCGCCTCGCCGCGCCGCA GGTTCTCCAGGACCGCCACGTTCAGCACCGACCCCTTGGCCATCGCCTCGCCTCGCCGCGCCGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14136397..14136600 26863196 MeRIP-seq:(Medium) rs267605304 Functional Loss SNV dbSNP153 33..33 33 - - - 82085 RMVar_ID_82085 Human_SNP_ID_659251219 m1A Human chr19 + 14160218 14160218 14160218 GCAGCTGCTCCATCAGCTTCACAGAGGAGGAGACGTCCCCCGCGTAGATGGAGCCCCGGGTGTGT GCAGCTGCTCCATCAGCTTCACAGAGGAGGAGTCGTCCCCCGCGTAGATGGAGCCCCGGGTGTGT A T AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14159751..14160340 32194978 MeRIP-seq:(Medium) rs752703138 Functional Loss SNV dbSNP153 33..33 33 - - - 82086 RMVar_ID_82086 Human_SNP_ID_659251393 m1A Human chr19 + 14160693 14160693 14160693 GCCCCAAGGCTGGTAGACACTGGAAGGAGGCAATTCCTGCAGGGACAGACAGACAGGAACAGACA GCCCCAAGGCTGGTAGACACTGGAAGGAGGCAGTTCCTGCAGGGACAGACAGACAGGAACAGACA A G AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14160691..14160866 26863196 MeRIP-seq:(Medium) rs532616784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587541 82087 RMVar_ID_82087 Human_SNP_ID_659251420 m1A Human chr19 + 14160740 14160738 14160741 GACAGACAGGAACAGACAAGGGAGCCAAAGGGAAGAAGAGAAGGATGGGACAGAGAGGGGGAAAG GACAGACAGGAACAGACAAGGGAGCCAAAGG___GAAGAGAAGGATGGGACAGAGAGGGGGAAAG GGAA G AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14160698..14160828 26863196 MeRIP-seq:(Medium) rs781675091 Functional Loss DEL dbSNP153 32..34 33 - - - 82088 RMVar_ID_82088 Human_SNP_ID_659251423 m1A Human chr19 + 14160740 14160740 14160740 GACAGACAGGAACAGACAAGGGAGCCAAAGGGAAGAAGAGAAGGATGGGACAGAGAGGGGGAAAG GACAGACAGGAACAGACAAGGGAGCCAAAGGGTAGAAGAGAAGGATGGGACAGAGAGGGGGAAAG A T AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14160698..14160828 26863196 MeRIP-seq:(Medium) rs766476412 Functional Loss SNV dbSNP153 33..33 33 - - - 82089 RMVar_ID_82089 Human_SNP_ID_659251731 m1A Human chr19 - 14161567 14161567 14161567 CGACCACCACAGCCAGGCCCACGCCCCTCACCAGCACAGCCTCGCCCGCAGCCACCACCCCGCTC CGACCACCACAGCCAGGCCCACGCCCCTCACCGGCACAGCCTCGCCCGCAGCCACCACCCCGCTC T C ADGRL1 Ensembl:ENSG00000072071 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14161351..14161654 26863196 MeRIP-seq:(Medium) rs1188585233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4505158 Human_Splice_Rec_1968120,Human_Splice_Rec_1968164 Human_miRNA_ID_1395773,Human_miRNA_ID_2716282,Human_miRNA_ID_3052267 RMVar_hsa_circ_120948,RMVar_hsa_circ_117388,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192981,RMVar_hsa_circ_192980 82090 RMVar_ID_82090 Human_SNP_ID_659252758 m1A Human chr19 - 14164339 14164339 14164339 CCCATACGCCCTTGTCTCTCTTCCCTCTGCACAGCTCTCCTCTCCCTCCCCAACTCTCCCGGGAG CCCATACGCCCTTGTCTCTCTTCCCTCTGCACGGCTCTCCTCTCCCTCCCCAACTCTCCCGGGAG T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14164320..14164521 26863196 MeRIP-seq:(Medium) rs1403268142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25442316 RMVar_hsa_circ_120948,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192980 82091 RMVar_ID_82091 Human_SNP_ID_659252898 m1A Human chr19 - 14164805 14164805 14164805 GTGTCTGGCCACACTGACCCCCGGATCAGTCAAGGGGAGGTTAGGAGTAGGTGGTGCTGGGACGT GTGTCTGGCCACACTGACCCCCGGATCAGTCAGGGGGAGGTTAGGAGTAGGTGGTGCTGGGACGT T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14164756..14164897 26863196 MeRIP-seq:(Medium) rs1238345701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120948,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192980 82092 RMVar_ID_82092 Human_SNP_ID_659253155 m1A Human chr19 + 14165732 14165732 14165732 GAGGAGACTGGAGGGGTGTGGTGAGGGGGCGGACCTGGGGCCAGCAGCCCAGGCCTCTCTGAGAT GAGGAGACTGGAGGGGTGTGGTGAGGGGGCGGGCCTGGGGCCAGCAGCCCAGGCCTCTCTGAGAT A G AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14165697..14165855 26863196 MeRIP-seq:(Medium) rs955469003 Functional Loss SNV dbSNP153 33..33 33 - - - 82093 RMVar_ID_82093 Human_SNP_ID_659253980 m1A Human chr19 - 14168441 14168441 14168441 CCCTTGGGGAGACAGGAGACACACGCACACACACACACGCGCAGACATGTGTGCACACATACGGG CCCTTGGGGAGACAGGAGACACACGCACACACGCACACGCGCAGACATGTGTGCACACATACGGG T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14168417..14168574 26863196 MeRIP-seq:(Medium) rs940373184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120948,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192980 82094 RMVar_ID_82094 Human_SNP_ID_659254460 m1A Human chr19 + 14170338 14170337 14170339 ATGGGGGAGAAAAGCATAGAGGCCAAGGGAGAAGAGAGAGACGTAAGTGTGCCAGGCAGAGCACG ATGGGGGAGAAAAGCATAGAGGCCAAGGGAGA__AGAGAGACGTAAGTGTGCCAGGCAGAGCACG AAG A AC022098.1 Ensembl:ENSG00000267169 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14170066..14170555 26863196 MeRIP-seq:(Medium) rs1309526600 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3589396,Human_RBP_ID_5587008 82095 RMVar_ID_82095 Human_SNP_ID_659254472 m1A Human chr19 + 14170359 14170359 14170359 GCCAAGGGAGAAGAGAGAGACGTAAGTGTGCCAGGCAGAGCACGGGACCATGGCCTGGCAGTGTG GCCAAGGGAGAAGAGAGAGACGTAAGTGTGCCGGGCAGAGCACGGGACCATGGCCTGGCAGTGTG A G AC022098.1 Ensembl:ENSG00000267169 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14170121..14170561 26863196 MeRIP-seq:(Medium) rs1057278120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589396,Human_RBP_ID_5587008 82096 RMVar_ID_82096 Human_SNP_ID_659255884 m1A Human chr19 + 14175464 14175462 14175464 AAAACACACACCTCAGTCAGCCACACCCGCTCACACACATGCTCACACCCACACCCGCTCACGTA AAAACACACACCTCAGTCAGCCACACCCGCT__CACACATGCTCACACCCACACCCGCTCACGTA TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14175461..14175593 26863196 MeRIP-seq:(Medium) rs201463957 Functional Loss DEL dbSNP153 32..33 33 - - - 82097 RMVar_ID_82097 Human_SNP_ID_659255886 m1A Human chr19 + 14175464 14175464 14175464 AAAACACACACCTCAGTCAGCCACACCCGCTCACACACATGCTCACACCCACACCCGCTCACGTA AAAACACACACCTCAGTCAGCCACACCCGCTCGCACACATGCTCACACCCACACCCGCTCACGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14175461..14175593 26863196 MeRIP-seq:(Medium) rs1184448954 Functional Loss SNV dbSNP153 33..33 33 - - - 82098 RMVar_ID_82098 Human_SNP_ID_659256566 m1A Human chr19 + 14177711 14177711 14177711 TGGGGTAGCCTTCACACGCCAGCTCCCGGCGCATCAGCCCGAACGGGAGCCCGGCCCGGCTCAGG TGGGGTAGCCTTCACACGCCAGCTCCCGGCGCGTCAGCCCGAACGGGAGCCCGGCCCGGCTCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14170623..14205987 32194978 MeRIP-seq:(Medium) rs138325009 Functional Loss SNV dbSNP153 33..33 33 - - - 82099 RMVar_ID_82099 Human_SNP_ID_659261783 m1A Human chr19 - 14195911 14195911 14195911 CCTGAGCCCCTGGAGGGACTGGGCTGCCATCCACTGAGCTGGAGGATGGGGCAGGGACTGGAGAT CCTGAGCCCCTGGAGGGACTGGGCTGCCATCCGCTGAGCTGGAGGATGGGGCAGGGACTGGAGAT T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14195909..14196249 26863196 MeRIP-seq:(Medium) rs1014216208 Functional Loss SNV dbSNP153 33..33 33 - - - 82100 RMVar_ID_82100 Human_SNP_ID_659262457 m1A Human chr19 + 14198610 14198610 14198610 GATCCTGACGCAAACCCCCTACCTCTACCCCCACCCCTGCCACAGGCCCTGGCAGCCCCACAGTC GATCCTGACGCAAACCCCCTACCTCTACCCCCCCCCCTGCCACAGGCCCTGGCAGCCCCACAGTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14198605..14198717 26863196 MeRIP-seq:(Medium) rs1040775675 Functional Loss SNV dbSNP153 33..33 33 - - - 82101 RMVar_ID_82101 Human_SNP_ID_659264650 m1A Human chr19 - 14206123 14206123 14206123 GCGGCGGTGCTGGGCCAGGGGAAGGAAGGGACACGGAGGCCGCCCTCGTCCCGCCACCTCCTACC GCGGCGGTGCTGGGCCAGGGGAAGGAAGGGACCCGGAGGCCGCCCTCGTCCCGCCACCTCCTACC T G ADGRL1 Ensembl:ENSG00000072071 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14205954..14206187 26863196 MeRIP-seq:(Medium) rs1229362805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241104,Human_RBP_ID_773351,Human_RBP_ID_4505251,Human_RBP_ID_5442707,Human_RBP_ID_8839157,Human_RBP_ID_9329841,Human_RBP_ID_26983845 82102 RMVar_ID_82102 Human_SNP_ID_659264738 m1A Human chr19 - 14206303 14206303 14206303 AGCCCCCGGCGCTCTGACGCCGCCCCCGCCCCACCGCCTCCCTCCCCGGGAGGGGCGCAGACCCG AGCCCCCGGCGCTCTGACGCCGCCCCCGCCCCCCCGCCTCCCTCCCCGGGAGGGGCGCAGACCCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14206174..14206378 26863196 MeRIP-seq:(Medium) rs1381552934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4562687 82103 RMVar_ID_82103 Human_SNP_ID_659264751 m1A Human chr19 - 14206335 14206335 14206335 CGGCGCCGCCTCGGGGCGCTCCGCCTCGCCCCAGCCCCCGGCGCTCTGACGCCGCCCCCGCCCCA CGGCGCCGCCTCGGGGCGCTCCGCCTCGCCCCCGCCCCCGGCGCTCTGACGCCGCCCCCGCCCCA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:14206236..14206407 26863196 MeRIP-seq:(Medium) rs1465643753 Functional Loss SNV dbSNP153 33..33 33 - - - 82104 RMVar_ID_82104 Human_SNP_ID_659264902 m1A Human chr19 - 14206695 14206695 14206695 ACCGGGGGCGCGACGCCGCGGCACCCGCCTCCAGCCGCGCCGCCCCCCTCCGCCAGCTCCGCGCC ACCGGGGGCGCGACGCCGCGGCACCCGCCTCCGGCCGCGCCGCCCCCCTCCGCCAGCTCCGCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14206653..14206817 26863196 MeRIP-seq:(Medium) rs1251143603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4562692 82105 RMVar_ID_82105 Human_SNP_ID_659264915 m1A Human chr19 + 14206736 14206736 14206736 GTGCCGCGGCGTCGCGCCCCCGGTGCGGCCGGAGGGGGGGCGCCGGGCCGGGCCCGTGGGCACCG GTGCCGCGGCGTCGCGCCCCCGGTGCGGCCGGGGGGGGGGCGCCGGGCCGGGCCCGTGGGCACCG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:14206551..14206825;chr19:14206498..14206800;chr19:14206706..14206868;chr19:14206699..14206837 26863410,26863196,26863196 MeRIP-seq:(Medium) rs941243631 Functional Loss SNV dbSNP153 33..33 33 - - - 82106 RMVar_ID_82106 Human_SNP_ID_659313404 m1A Human chr19 - 14381556 14381556 14381556 TGGAGCTTCCTCGCCCCTCCCAGCGGGGCCCCAAAGTACTTACCGAGAAAGACGCGGCCTCCCAT TGGAGCTTCCTCGCCCCTCCCAGCGGGGCCCCTAAGTACTTACCGAGAAAGACGCGGCCTCCCAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14381526..14381625 26863196 MeRIP-seq:(Medium) rs1337668333 Functional Loss SNV dbSNP153 33..33 33 - - - 82107 RMVar_ID_82107 Human_SNP_ID_659315834 m1A Human chr19 + 14389390 14389390 14389390 GGATGAGGAGGGAGACGGGGAAGGGGAGGGGGAGGCAGAGGGAGAGGAAAGGAGGCAGGAAGGAA GGATGAGGAGGGAGACGGGGAAGGGGAGGGGGGGGCAGAGGGAGAGGAAAGGAGGCAGGAAGGAA A G ADGRE5 Ensembl:ENSG00000123146 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14389385..14389620 26863196 MeRIP-seq:(Medium) rs1240308808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263841,Human_RBP_ID_8196175,Human_RBP_ID_9427106 RMVar_hsa_circ_81043,RMVar_hsa_circ_19864,RMVar_hsa_circ_192998,RMVar_hsa_circ_25743 82108 RMVar_ID_82108 Human_SNP_ID_659316995 m1A Human chr19 - 14393511 14393511 14393511 CTCTTTGAATGAGTCGCAGCTCCCAGCTGCCCACTGCTGGCTCCCATCTGCCCCTGTGAATCCTG CTCTTTGAATGAGTCGCAGCTCCCAGCTGCCCGCTGCTGGCTCCCATCTGCCCCTGTGAATCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14393501..14393625 26863196 MeRIP-seq:(Medium) rs891128610 Functional Loss SNV dbSNP153 33..33 33 - - - 82109 RMVar_ID_82109 Human_SNP_ID_659316996 m1A Human chr19 - 14393511 14393511 14393511 CTCTTTGAATGAGTCGCAGCTCCCAGCTGCCCACTGCTGGCTCCCATCTGCCCCTGTGAATCCTG CTCTTTGAATGAGTCGCAGCTCCCAGCTGCCCCCTGCTGGCTCCCATCTGCCCCTGTGAATCCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14393501..14393625 26863196 MeRIP-seq:(Medium) rs891128610 Functional Loss SNV dbSNP153 33..33 33 - - - 82110 RMVar_ID_82110 Human_SNP_ID_659319838 m1A Human chr19 - 14402703 14402703 14402703 CGTCTGAGTTGGACACCACGGATGCTGCTTTCATATATCTCCTCCAGTTCGGCTTGCTTCTTGGA CGTCTGAGTTGGACACCACGGATGCTGCTTTCGTATATCTCCTCCAGTTCGGCTTGCTTCTTGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14402653..14402896 26863196 MeRIP-seq:(Medium) rs368849819 Functional Loss SNV dbSNP153 33..33 33 - - - 82111 RMVar_ID_82111 Human_SNP_ID_659321733 m1A Human chr19 + 14408182 14408182 14408182 CTCCTGTGGCCACAGCAGCTTTGTACACGAAGACCATCCATCCTCCCTTCGTCCACCACTCTACT CTCCTGTGGCCACAGCAGCTTTGTACACGAAGTCCATCCATCCTCCCTTCGTCCACCACTCTACT A T ADGRE5 Ensembl:ENSG00000123146 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14408133..14408230 26863196 MeRIP-seq:(Medium) rs977018115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24483678,Human_RBP_ID_26465094,Human_RBP_ID_27464141 Human_Splice_Rec_1968300,Human_Splice_Rec_1968368,Human_Splice_Rec_1968414 Human_miRNA_ID_1957699,Human_miRNA_ID_2030582,Human_miRNA_ID_2467541,Human_miRNA_ID_2691031,Human_miRNA_ID_2694350 RMVar_hsa_circ_123178,RMVar_hsa_circ_193005 82112 RMVar_ID_82112 Human_SNP_ID_659321943 m1A Human chr19 - 14408907 14408907 14408907 GTAACCACCACGTGCCAGAGCCGCCCACCCGGAGCCGCCCGCATGCAGCTTCACCTCCCCTTTCC GTAACCACCACGTGCCAGAGCCGCCCACCCGGTGCCGCCCGCATGCAGCTTCACCTCCCCTTTCC T A DDX39A Ensembl:ENSG00000123136 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14408857..14409166 26863196 MeRIP-seq:(Medium) rs768282153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773770,Human_RBP_ID_27268808 Human_Splice_Rec_1968458,Human_Splice_Rec_1968464,Human_Splice_Rec_1968482,Human_Splice_Rec_1968498,Human_Splice_Rec_1968516 82113 RMVar_ID_82113 Human_SNP_ID_659321944 m1A Human chr19 - 14408907 14408907 14408907 GTAACCACCACGTGCCAGAGCCGCCCACCCGGAGCCGCCCGCATGCAGCTTCACCTCCCCTTTCC GTAACCACCACGTGCCAGAGCCGCCCACCCGGCGCCGCCCGCATGCAGCTTCACCTCCCCTTTCC T G DDX39A Ensembl:ENSG00000123136 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14408857..14409166 26863196 MeRIP-seq:(Medium) rs768282153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773770,Human_RBP_ID_27268808 Human_Splice_Rec_1968458,Human_Splice_Rec_1968464,Human_Splice_Rec_1968482,Human_Splice_Rec_1968498,Human_Splice_Rec_1968516 82114 RMVar_ID_82114 Human_SNP_ID_659322489 m1A Human chr19 - 14410322 14410322 14410322 GTCTTGCCCTCCCCACCTAGACATGCGGCGGGATGTGCAGGAGATCTTCCGCCTGACACCACACG GTCTTGCCCTCCCCACCTAGACATGCGGCGGGTTGTGCAGGAGATCTTCCGCCTGACACCACACG T A DDX39A Ensembl:ENSG00000123136 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14410276..14410663 32194978 MeRIP-seq:(Medium) rs1418561453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771091,Human_RBP_ID_907423,Human_RBP_ID_5370069,Human_RBP_ID_9382133,Human_RBP_ID_22546651,Human_RBP_ID_22662241,Human_RBP_ID_22742435,Human_RBP_ID_26335871 Human_Splice_Rec_1968448,Human_Splice_Rec_1968474,Human_Splice_Rec_1968492,Human_Splice_Rec_1968506,Human_Splice_Rec_1968522,Human_Splice_Rec_1968532,Human_Splice_Rec_1968546,Human_Splice_Rec_1968556,Human_Splice_Rec_1968568,Human_Splice_Rec_1968572,Human_Splice_Rec_1968580 RMVar_hsa_circ_3830,RMVar_hsa_circ_70824,RMVar_hsa_circ_193006,RMVar_hsa_circ_372402 82115 RMVar_ID_82115 Human_SNP_ID_659322734 m1A Human chr19 + 14411104 14411104 14411104 GCCAGGATGCGGCCCGGGGTCCCCACCACGACATGGGGACAGTTCTTCTTCAACACTTCTTCATC GCCAGGATGCGGCCCGGGGTCCCCACCACGACGTGGGGACAGTTCTTCTTCAACACTTCTTCATC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:14410976..14411191 26863196 MeRIP-seq:(Medium) rs1449391005 Functional Loss SNV dbSNP153 33..33 33 - - - 82116 RMVar_ID_82116 Human_SNP_ID_659322758 m1A Human chr19 + 14411160 14411160 14411160 TTCTTCATCCTTCTTGATGGAGAGACCACCGAAGAACACAGACACCTATGGGGATGAGGAGGAAA TTCTTCATCCTTCTTGATGGAGAGACCACCGACGAACACAGACACCTATGGGGATGAGGAGGAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:14411110..14411211 32194978 MeRIP-seq:(Medium) rs774188639 Functional Loss SNV dbSNP153 33..33 33 - - - 82117 RMVar_ID_82117 Human_SNP_ID_659323217 m1A Human chr19 - 14412680 14412680 14412680 GGTTCTCGTCCCTCACGCTCTGCTTCTCCTGCAGTCCAGCATGAGTGCATTCCCCAGGCCATCCT GGTTCTCGTCCCTCACGCTCTGCTTCTCCTGCGGTCCAGCATGAGTGCATTCCCCAGGCCATCCT T C DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr19:14412651..14412700;chr19:14412651..14412968 26863196,32194978 MeRIP-seq:(Medium) rs879098424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3956442,Human_RBP_ID_22545705,Human_RBP_ID_22666457,Human_RBP_ID_27268825 Human_Splice_Rec_1968562 RMVar_hsa_circ_3830,RMVar_hsa_circ_193008,RMVar_hsa_circ_14736,RMVar_hsa_circ_193006,RMVar_hsa_circ_372402,RMVar_hsa_circ_369858,RMVar_hsa_circ_342976 82118 RMVar_ID_82118 Human_SNP_ID_659323372 m1A Human chr19 - 14413148 14413148 14413148 ATGAAGAGGAAGAGCCCCAGGCTCCTCAAGAGAGCACACCAGCTCCCCCTAAGAAAGACATCAAG ATGAAGAGGAAGAGCCCCAGGCTCCTCAAGAGTGCACACCAGCTCCCCCTAAGAAAGACATCAAG T A DDX39A Ensembl:ENSG00000123136 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:14413101..14413175 26863196 MeRIP-seq:(Medium) rs1451785712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55198,Human_RBP_ID_908493,Human_RBP_ID_4562764,Human_RBP_ID_18412303,Human_RBP_ID_18544488,Human_RBP_ID_24545448,Human_RBP_ID_27816196 Human_Splice_Rec_1968440,Human_Splice_Rec_1968466,Human_Splice_Rec_1968484,Human_Splice_Rec_1968536,Human_Splice_Rec_1968548,Human_Splice_Rec_1968560,Human_Splice_Rec_1968584,Human_Splice_Rec_1968590,Human_Splice_Rec_1968596,Human_Splice_Rec_1968604,Human_Splice_Rec_1968610,Human_Splice_Rec_1968614,Human_Splice_Rec_1968618,Human_Splice_Rec_1968624 Human_miRNA_ID_2052714 RMVar_hsa_circ_3830,RMVar_hsa_circ_193008,RMVar_hsa_circ_14736,RMVar_hsa_circ_193006,RMVar_hsa_circ_372402,RMVar_hsa_circ_369858,RMVar_hsa_circ_342976 82119 RMVar_ID_82119 Human_SNP_ID_659329253 m1A Human chr19 - 14433420 14433420 14433420 GGGCGTGGCGGGGAGGGGGCGGGCGCGGCGCGACCCTCCCCGGCGCGCGGCCCGCTCCGGCCTGC GGGCGTGGCGGGGAGGGGGCGGGCGCGGCGCGCCCCTCCCCGGCGCGCGGCCCGCTCCGGCCTGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEK293T,untreat control;HEPG2 cell line,mRNA heat shock 4h chr19:14433325..14433580;chr19:14433329..14433502;chr19:14433387..14433598 26863410,26863196 MeRIP-seq:(Medium) rs1019040243 Functional Loss SNV dbSNP153 33..33 33 - - - 82120 RMVar_ID_82120 Human_SNP_ID_659329262 m1A Human chr19 - 14433439 14433439 14433439 AGGAGCGCGCGTGCGCCCCGGGCGTGGCGGGGAGGGGGCGGGCGCGGCGCGACCCTCCCCGGCGC AGGAGCGCGCGTGCGCCCCGGGCGTGGCGGGGGGGGGGCGGGCGCGGCGCGACCCTCCCCGGCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:14433341..14434648 26863410 MeRIP-seq:(Medium) rs996356964 Functional Loss SNV dbSNP153 33..33 33 - - - 82121 RMVar_ID_82121 Human_SNP_ID_659329293 m1A Human chr19 - 14433523 14433523 14433523 CAGGTGCGCCTACCTGCACGGCGTCGCTGGCCATGTCCTCCTGCCGCCCGCCAGGGGTCCCCGCG CAGGTGCGCCTACCTGCACGGCGTCGCTGGCCCTGTCCTCCTGCCGCCCGCCAGGGGTCCCCGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14433476..14433550 32194978 MeRIP-seq:(Medium) rs1235576890 Functional Loss SNV dbSNP153 33..33 33 - - - 82122 RMVar_ID_82122 Human_SNP_ID_659331321 m1A Human chr19 + 14441240 14441240 14441240 CGGGGTACAGCAGCAGCTGGAGCTGGAGCGGGAGCGGCTGCGGCGGGAAATCCGCAAGGAGCTGA CGGGGTACAGCAGCAGCTGGAGCTGGAGCGGGGGCGGCTGCGGCGGGAAATCCGCAAGGAGCTGA A G PKN1 Ensembl:ENSG00000123143 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14441094..14441393 26863196 MeRIP-seq:(Medium) rs746350154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239955,Human_RBP_ID_4557280,Human_RBP_ID_5239273,Human_RBP_ID_5320219,Human_RBP_ID_8839159,Human_RBP_ID_9328717,Human_RBP_ID_18994475 Human_Splice_Rec_1968628,Human_Splice_Rec_1968634,Human_Splice_Rec_1968676,Human_Splice_Rec_1968714,Human_Splice_Rec_1968724,Human_Splice_Rec_1968732,Human_Splice_Rec_1968740,Human_Splice_Rec_1968782 RMVar_hsa_circ_24080,RMVar_hsa_circ_349042,RMVar_hsa_circ_358871,RMVar_hsa_circ_81540,RMVar_hsa_circ_193010,RMVar_hsa_circ_193011 82123 RMVar_ID_82123 Human_SNP_ID_659332105 m1A Human chr19 - 14443558 14443558 14443558 ATGTTCTCCGCCCCCTGCTTCACCTTCAGCTCAATGGCCAACTGCTTCTCCAGGCCCGCCACGCG ATGTTCTCCGCCCCCTGCTTCACCTTCAGCTCCATGGCCAACTGCTTCTCCAGGCCCGCCACGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14441126..14463565 32194978 MeRIP-seq:(Medium) rs772254067 Functional Loss SNV dbSNP153 33..33 33 - - - 82124 RMVar_ID_82124 Human_SNP_ID_659333915 m1A Human chr19 - 14450414 14450414 14450414 GGTCCGGGGCCTTGGCAGCGCTGAGCAGGCGCAGTACGTTCTTGGCACCCTCGGCCACCGCGTGC GGTCCGGGGCCTTGGCAGCGCTGAGCAGGCGCTGTACGTTCTTGGCACCCTCGGCCACCGCGTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14450367..14450501 26863196 MeRIP-seq:(Medium) rs1217295997 Functional Loss SNV dbSNP153 33..33 33 - - - 82125 RMVar_ID_82125 Human_SNP_ID_659334170 m1A Human chr19 + 14451008 14451008 14451008 CGCCGACCACCCCAAGGGGCGGCTGCTGCGAGAAGAGCTCGCTGCGGCCTCCTCCGCTGCCTTCA CGCCGACCACCCCAAGGGGCGGCTGCTGCGAGGAGAGCTCGCTGCGGCCTCCTCCGCTGCCTTCA A G PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14450957..14451100 26863196 MeRIP-seq:(Medium) rs745803101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239959,Human_RBP_ID_4505578,Human_RBP_ID_9294274,Human_RBP_ID_17915890 RMVar_hsa_circ_6466,RMVar_hsa_circ_81540,RMVar_hsa_circ_124635,RMVar_hsa_circ_193010,RMVar_hsa_circ_18687,RMVar_hsa_circ_193013,RMVar_hsa_circ_193012,RMVar_hsa_circ_302755 82126 RMVar_ID_82126 Human_SNP_ID_659334215 m1A Human chr19 + 14451074 14451074 14451074 CACCCGCCTGGCCGGGCCCTTTCCCGCCACGCACTACAGCACCCTGTGCAAGCCCGCGCCGCTCA CACCCGCCTGGCCGGGCCCTTTCCCGCCACGCTCTACAGCACCCTGTGCAAGCCCGCGCCGCTCA A T PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:14451035..14451904 26863410 MeRIP-seq:(Medium) rs1027732937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8839163,Human_RBP_ID_9294275,Human_RBP_ID_18470708,Human_RBP_ID_27268833 Human_Splice_Rec_1968643,Human_Splice_Rec_1968685,Human_Splice_Rec_1968749,Human_Splice_Rec_1968783 RMVar_hsa_circ_6466,RMVar_hsa_circ_81540,RMVar_hsa_circ_124635,RMVar_hsa_circ_193010,RMVar_hsa_circ_18687,RMVar_hsa_circ_193013,RMVar_hsa_circ_193012,RMVar_hsa_circ_302755 82127 RMVar_ID_82127 Human_SNP_ID_659334482 m1A Human chr19 - 14451901 14451901 14451901 GGGGGCGGCTGTCTGGGGTCCCAGGTCCCCCCATTGAGGGGGTAGGGTTCCACGGGATGGTCTCT GGGGGCGGCTGTCTGGGGTCCCAGGTCCCCCCTTTGAGGGGGTAGGGTTCCACGGGATGGTCTCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14451851..14451900 26863196 MeRIP-seq:(Medium) rs773869914 Functional Loss SNV dbSNP153 33..33 33 - - - 82128 RMVar_ID_82128 Human_SNP_ID_659340053 m1A Human chr19 + 14470838 14470838 14470838 TAGCGAGAGAGATGCAGAAGATGTGAAGAAACAGCCCTTCTTCAGGGTGAGATTCCCCACAAGGA TAGCGAGAGAGATGCAGAAGATGTGAAGAAACTGCCCTTCTTCAGGGTGAGATTCCCCACAAGGA A T PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14470718..14470878 26863196 MeRIP-seq:(Medium) rs966216895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3954612,Human_RBP_ID_17934891,Human_RBP_ID_18412304,Human_RBP_ID_18994482,Human_RBP_ID_19092501 Human_Splice_Rec_1968672,Human_Splice_Rec_1968673,Human_Splice_Rec_1968708,Human_Splice_Rec_1968709,Human_Splice_Rec_1968778,Human_Splice_Rec_1968779,Human_Splice_Rec_1968816,Human_Splice_Rec_1968817,Human_Splice_Rec_1968821,Human_Splice_Rec_1968823 82129 RMVar_ID_82129 Human_SNP_ID_659340510 m1A Human chr19 + 14471714 14471714 14471714 CGGGGAGGCCCCCACACTGAGCCCGCCCCGCGACGCGCGGCCCCTCACAGCCGCGGAGCAGGCAG CGGGGAGGCCCCCACACTGAGCCCGCCCCGCGGCGCGCGGCCCCTCACAGCCGCGGAGCAGGCAG A G PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:14471558..14471850;chr19:14471669..14471756 26863196 MeRIP-seq:(Medium) rs771516281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514377,Human_RBP_ID_9293472,Human_RBP_ID_18192066,Human_RBP_ID_26815419 82130 RMVar_ID_82130 Human_SNP_ID_659343044 m1A Human chr19 - 14478543 14478543 14478543 CCCAATAGCGGCCACCATGGTGGAGCTGGGAAAGGACAAAAGGAACCCGGATGAGCTGGCCGAGG CCCAATAGCGGCCACCATGGTGGAGCTGGGAAGGGACAAAAGGAACCCGGATGAGCTGGCCGAGG T C GIPC1 Ensembl:ENSG00000123159 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:14477876..14478575;chr19:14478100..14478577;chr19:14477895..14478587 26863196 MeRIP-seq:(Medium) rs1362893794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908495,Human_RBP_ID_18996910 Human_Splice_Rec_1968840,Human_Splice_Rec_1968856,Human_Splice_Rec_1968868,Human_Splice_Rec_1968872,Human_Splice_Rec_1968878,Human_Splice_Rec_1968892,Human_Splice_Rec_1968904,Human_Splice_Rec_1968916 Human_miRNA_ID_2255663 RMVar_hsa_circ_80215,RMVar_hsa_circ_108720,RMVar_hsa_circ_125413,RMVar_hsa_circ_112694,RMVar_hsa_circ_89679,RMVar_hsa_circ_193022,RMVar_hsa_circ_193024,RMVar_hsa_circ_193026,RMVar_hsa_circ_77127,RMVar_hsa_circ_193025,RMVar_hsa_circ_193023,RMVar_hsa_circ_193021 82131 RMVar_ID_82131 Human_SNP_ID_659343088 m1A Human chr19 - 14478661 14478661 14478661 ACGGAGCTGGGTGAGTGAGGGCTGCCTGGGGGAGGGGGCATCTAGGTCTGCTGGGGGCCGAATCC ACGGAGCTGGGTGAGTGAGGGCTGCCTGGGGGCGGGGGCATCTAGGTCTGCTGGGGGCCGAATCC T G GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14478657..14478775 26863196 MeRIP-seq:(Medium) rs753675454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_108720,RMVar_hsa_circ_125413,RMVar_hsa_circ_89679,RMVar_hsa_circ_193022,RMVar_hsa_circ_193024,RMVar_hsa_circ_193026,RMVar_hsa_circ_77127,RMVar_hsa_circ_193025,RMVar_hsa_circ_193023 82132 RMVar_ID_82132 Human_SNP_ID_659343282 m1A Human chr19 + 14479366 14479358 14479367 AAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAGAAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAGAGTGAGACTCTGTCTCAAAAAA_________AAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAAAAAAAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14479364..14479463 26863196 MeRIP-seq:(Medium) rs1461878716 Functional Loss DEL dbSNP153 26..34 33 - - - 82133 RMVar_ID_82133 Human_SNP_ID_659343284 m1A Human chr19 + 14479366 14479363 14479367 AAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAGAAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAGAGTGAGACTCTGTCTCAAAAAAAAAAA____AAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14479364..14479463 26863196 MeRIP-seq:(Medium) rs1411040604 Functional Loss DEL dbSNP153 31..34 33 - - - 82134 RMVar_ID_82134 Human_SNP_ID_659343285 m1A Human chr19 + 14479366 14479365 14479367 AAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAGAAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAGAGTGAGACTCTGTCTCAAAAAAAAAAAAA__AAAGGGAAGGGATGCCGGAGATAGGGTCCGG AAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14479364..14479463 26863196 MeRIP-seq:(Medium) rs1491175387 Functional Loss DEL dbSNP153 33..34 33 - - - 82135 RMVar_ID_82135 Human_SNP_ID_659344409 m1A Human chr19 - 14482664 14482664 14482664 CTGCCGAGGTATCCACTGGGGAGCCGGGCACCAGGGTCCCTGATGGTGGACCAGAGGTCTGGGCC CTGCCGAGGTATCCACTGGGGAGCCGGGCACCTGGGTCCCTGATGGTGGACCAGAGGTCTGGGCC T A GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14482659..14482800 26863196 MeRIP-seq:(Medium) rs1436321783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19089470 RMVar_hsa_circ_80215,RMVar_hsa_circ_89679,RMVar_hsa_circ_193026,RMVar_hsa_circ_193025,RMVar_hsa_circ_88431,RMVar_hsa_circ_50718,RMVar_hsa_circ_193028 82136 RMVar_ID_82136 Human_SNP_ID_659344422 m1A Human chr19 + 14482680 14482680 14482680 CCACCATCAGGGACCCTGGTGCCCGGCTCCCCAGTGGATACCTCGGCAGTTGGCAGGCGGAAGGC CCACCATCAGGGACCCTGGTGCCCGGCTCCCCGGTGGATACCTCGGCAGTTGGCAGGCGGAAGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14482676..14482825 26863196 MeRIP-seq:(Medium) rs775977495 Functional Loss SNV dbSNP153 33..33 33 - - - 82137 RMVar_ID_82137 Human_SNP_ID_659344610 m1A Human chr19 + 14483003 14483003 14483003 CGGCATGAGCAGCGAGAAGTGGGGTCACCAGAAGATCTGCAGGACAGGAAGTGGGGCTCAGGGCC CGGCATGAGCAGCGAGAAGTGGGGTCACCAGATGATCTGCAGGACAGGAAGTGGGGCTCAGGGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:14482851..14483041;chr19:14482812..14483063;chr19:14482851..14483063 26863196 MeRIP-seq:(Medium) rs762109304 Functional Loss SNV dbSNP153 33..33 33 - - - 82138 RMVar_ID_82138 Human_SNP_ID_659346491 m1A Human chr19 - 14488888 14488888 14488888 GCAACCTGTTACCTCCCTGCCCTCATGTTCTCACTATCCCCCCTTCACTCACTGTTCCAACCCCC GCAACCTGTTACCTCCCTGCCCTCATGTTCTCGCTATCCCCCCTTCACTCACTGTTCCAACCCCC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14488885..14489089 26863196 MeRIP-seq:(Medium) rs1444020806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 82139 RMVar_ID_82139 Human_SNP_ID_659347436 m1A Human chr19 - 14491715 14491712 14491715 ACAGGACCATTCTGGCTGCTGTCTGGACAAGAAGTCGTAGGGGGTGAGGGTGGAAGCTGGGAAAC ACAGGACCATTCTGGCTGCTGTCTGGACAAGA___CGTAGGGGGTGAGGGTGGAAGCTGGGAAAC GACT G GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14491601..14491793 26863196 MeRIP-seq:(Medium) rs1178941370 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_914466,Human_RBP_ID_4562827,Human_RBP_ID_8829985,Human_RBP_ID_13377573,Human_RBP_ID_23783995 Human_Splice_Rec_1968844,Human_Splice_Rec_1968845,Human_Splice_Rec_1968880,Human_Splice_Rec_1968881,Human_Splice_Rec_1968894,Human_Splice_Rec_1968895,Human_Splice_Rec_1968908,Human_Splice_Rec_1968909,Human_Splice_Rec_1968925 Human_miRNA_ID_2660579 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_193029,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028,RMVar_hsa_circ_280924 82140 RMVar_ID_82140 Human_SNP_ID_659347439 m1A Human chr19 + 14491713 14491713 14491713 GGGTTTCCCAGCTTCCACCCTCACCCCCTACGACTTCTTGTCCAGACAGCAGCCAGAATGGTCCT GGGTTTCCCAGCTTCCACCCTCACCCCCTACGGCTTCTTGTCCAGACAGCAGCCAGAATGGTCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:14491595..14496150;chr19:14491563..14491808 26863196 MeRIP-seq:(Medium) rs1440234367 Functional Loss SNV dbSNP153 33..33 33 - - - 82141 RMVar_ID_82141 Human_SNP_ID_659348671 m1A Human chr19 - 14496076 14496046 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC______________________________GGC CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1568371588 Functional Loss DEL dbSNP153 33..62 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82142 RMVar_ID_82142 Human_SNP_ID_659348679 m1A Human chr19 - 14496080 14496050 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGG______________________________CGG GCCGCCGCCGCCGCCGCCGCCGCCGCTGCCT G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs1432944260 Functional Loss DEL dbSNP153 33..62 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82143 RMVar_ID_82143 Human_SNP_ID_659348683 m1A Human chr19 - 14496076 14496052 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC________________________GGCGGCGGC CGCCGCCGCCGCCGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1403608563 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82144 RMVar_ID_82144 Human_SNP_ID_659348688 m1A Human chr19 - 14496076 14496055 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC_____________________GGCGGCGGCGGC CGCCGCCGCCGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1029777368 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82145 RMVar_ID_82145 Human_SNP_ID_659348693 m1A Human chr19 - 14496076 14496058 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC__________________GGCGGCGGCGGCGGC CGCCGCCGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1020489392 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82146 RMVar_ID_82146 Human_SNP_ID_659348703 m1A Human chr19 - 14496076 14496061 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC_______________GGCGGCGGCGGCGGCGGC CGCCGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1034420562 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82147 RMVar_ID_82147 Human_SNP_ID_659348710 m1A Human chr19 - 14496080 14496062 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGG__________________CGGCGGCGGCGGCGG GCCGCCGCCGCCGCTGCCT G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs954181558 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82148 RMVar_ID_82148 Human_SNP_ID_659348714 m1A Human chr19 - 14496076 14496064 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC____________GGCGGCGGCGGCGGCGGCGGC CGCCGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs534895121 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82149 RMVar_ID_82149 Human_SNP_ID_659348721 m1A Human chr19 - 14496076 14496067 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC_________GGCGGCGGCGGCGGCGGCGGCGGC CGCCGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1159069531 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82150 RMVar_ID_82150 Human_SNP_ID_659348723 m1A Human chr19 - 14496080 14496068 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGG____________CGGCGGCGGCGGCGGCGGCGG GCCGCCGCTGCCT G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs1007094162 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82151 RMVar_ID_82151 Human_SNP_ID_659348726 m1A Human chr19 - 14496076 14496070 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC______GGCGGCGGCGGCGGCGGCGGCGGCGGC CGCCGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs1454466737 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82152 RMVar_ID_82152 Human_SNP_ID_659348737 m1A Human chr19 - 14496076 14496073 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGC___GGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CGCT C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs781618301 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82153 RMVar_ID_82153 Human_SNP_ID_659348739 m1A Human chr19 - 14496080 14496074 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGG______CGGCGGCGGCGGCGGCGGCGGCGGCGG GCTGCCT G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs1367422954 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82154 RMVar_ID_82154 Human_SNP_ID_659348747 m1A Human chr19 - 14496076 14496076 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs540479273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82155 RMVar_ID_82155 Human_SNP_ID_659348757 m1A Human chr19 - 14496080 14496080 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGGGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG T C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs574293970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82156 RMVar_ID_82156 Human_SNP_ID_659348758 m1A Human chr19 - 14496080 14496080 14496080 GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG GAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGG T G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:14491676..14496108 26863410 MeRIP-seq:(Medium) rs574293970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82157 RMVar_ID_82157 Human_SNP_ID_659348763 m1A Human chr19 - 14496086 14496086 14496086 TTTGCGGAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGG TTTGCGGAGGGCCGAGCCGGGTGCGCACGGGGGGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGG T C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:14495882..14496306;chr19:14495882..14496288;chr19:14495954..14496125 26863196 MeRIP-seq:(Medium) rs1010351732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82158 RMVar_ID_82158 Human_SNP_ID_659348764 m1A Human chr19 - 14496086 14496086 14496086 TTTGCGGAGGGCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGG TTTGCGGAGGGCCGAGCCGGGTGCGCACGGGGCGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGG T G GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:14495882..14496306;chr19:14495882..14496288;chr19:14495954..14496125 26863196 MeRIP-seq:(Medium) rs1010351732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 82159 RMVar_ID_82159 Human_SNP_ID_659355430 m1A Human chr19 + 14517288 14517288 14517288 AAAAGGACTCATGCGGTTAGGTGTTCACCTCCAGGTGCCACCTAGGCCCTGCCACTCCTGGACTG AAAAGGACTCATGCGGTTAGGTGTTCACCTCCGGGTGCCACCTAGGCCCTGCCACTCCTGGACTG A G TECR Ensembl:ENSG00000099797 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14517284..14529860 32194978 MeRIP-seq:(Medium) rs1157370863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1968975 82160 RMVar_ID_82160 Human_SNP_ID_659355921 m1A Human chr19 - 14518258 14518258 14518258 CAAGCGGGCCTACCGCCGCCAGGCGCTGCGCTACCACCCGGACAAGAACAAGGAGCCCGGCGCCG CAAGCGGGCCTACCGCCGCCAGGCGCTGCGCTGCCACCCGGACAAGAACAAGGAGCCCGGCGCCG T C DNAJB1 Ensembl:ENSG00000132002 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14518092..14518425 26863196 MeRIP-seq:(Medium) rs748402159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4505944,Human_RBP_ID_8942193,Human_RBP_ID_9380688,Human_RBP_ID_22448470,Human_RBP_ID_26335882,Human_RBP_ID_27268903,Human_RBP_ID_27562037,Human_RBP_ID_27816200 Human_Splice_Rec_1968970 RMVar_hsa_circ_95237,RMVar_hsa_circ_88931,RMVar_hsa_circ_193032,RMVar_hsa_circ_193033 82161 RMVar_ID_82161 Human_SNP_ID_659355968 m1A Human chr19 + 14518325 14518325 14518325 CTCCTCGTCCGACGCGCCGCGGGCCAGGCCCAACGTCTGGTAGTAGTCTTTACCCATGACCCCCT CTCCTCGTCCGACGCGCCGCGGGCCAGGCCCACCGTCTGGTAGTAGTCTTTACCCATGACCCCCT A C TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:14518226..14518425 26863196 MeRIP-seq:(Medium) rs778361162 Functional Loss SNV dbSNP153 33..33 33 - - - 82162 RMVar_ID_82162 Human_SNP_ID_659355969 m1A Human chr19 + 14518325 14518325 14518325 CTCCTCGTCCGACGCGCCGCGGGCCAGGCCCAACGTCTGGTAGTAGTCTTTACCCATGACCCCCT CTCCTCGTCCGACGCGCCGCGGGCCAGGCCCAGCGTCTGGTAGTAGTCTTTACCCATGACCCCCT A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:14518226..14518425 26863196 MeRIP-seq:(Medium) rs778361162 Functional Loss SNV dbSNP153 33..33 33 - - - 82163 RMVar_ID_82163 Human_SNP_ID_659355978 m1A Human chr19 + 14518334 14518334 14518334 CGACGCGCCGCGGGCCAGGCCCAACGTCTGGTAGTAGTCTTTACCCATGACCCCCTCCTGCGGCC CGACGCGCCGCGGGCCAGGCCCAACGTCTGGTGGTAGTCTTTACCCATGACCCCCTCCTGCGGCC A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:14518176..14518425 26863196 MeRIP-seq:(Medium) rs1207240675 Functional Loss SNV dbSNP153 33..33 33 - - - 82164 RMVar_ID_82164 Human_SNP_ID_659355985 m1A Human chr19 + 14518344 14518344 14518344 CGGGCCAGGCCCAACGTCTGGTAGTAGTCTTTACCCATGACCCCCTCCTGCGGCCCGCCGACCCG CGGGCCAGGCCCAACGTCTGGTAGTAGTCTTTCCCCATGACCCCCTCCTGCGGCCCGCCGACCCG A C TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:14517926..14518450;chr19:14518201..14518414 26863196 MeRIP-seq:(Medium) rs747769161 Functional Loss SNV dbSNP153 33..33 33 - - - 82165 RMVar_ID_82165 Human_SNP_ID_659361344 m1A Human chr19 - 14536755 14536755 14536755 GACAATTATCCCAGTCAATATGAACATTGGGCAGGAGAGAGGAAGGGGCCTCAGCTGTAGCATTT GACAATTATCCCAGTCAATATGAACATTGGGCCGGAGAGAGGAAGGGGCCTCAGCTGTAGCATTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14536753..14537164 26863196 MeRIP-seq:(Medium) rs1012513220 Functional Loss SNV dbSNP153 33..33 33 - - - 82166 RMVar_ID_82166 Human_SNP_ID_659361363 m1A Human chr19 - 14536827 14536827 14536827 CCAGGTATGTATCTGCTCATACGATGCTCACCAGACCAAGAAACCCTTGAAACGATAACCCTGGG CCAGGTATGTATCTGCTCATACGATGCTCACCGGACCAAGAAACCCTTGAAACGATAACCCTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14536825..14537184 26863196 MeRIP-seq:(Medium) rs1428632757 Functional Loss SNV dbSNP153 33..33 33 - - - 82167 RMVar_ID_82167 Human_SNP_ID_659361372 m1A Human chr19 - 14536853 14536853 14536853 AAGGTGCTGCACCAAGCTGAGGCTTTCCAGGTATGTATCTGCTCATACGATGCTCACCAGACCAA AAGGTGCTGCACCAAGCTGAGGCTTTCCAGGTCTGTATCTGCTCATACGATGCTCACCAGACCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14536851..14537168 26863196 MeRIP-seq:(Medium) rs968683919 Functional Loss SNV dbSNP153 33..33 33 - - - 82168 RMVar_ID_82168 Human_SNP_ID_659361403 m1A Human chr19 - 14536954 14536952 14536955 CGGCCCCGCCCCCTCCTCGGCCCCTCCTCCCCACATCTGCCCCGTGTCCAGAGGTCCAGAGGTGA CGGCCCCGCCCCCTCCTCGGCCCCTCCTCCC___ATCTGCCCCGTGTCCAGAGGTCCAGAGGTGA TGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:14536941..14537160 26863196 MeRIP-seq:(Medium) rs977677967 Functional Loss DEL dbSNP153 32..34 33 - - - 82169 RMVar_ID_82169 Human_SNP_ID_659361404 m1A Human chr19 - 14536954 14536954 14536954 CGGCCCCGCCCCCTCCTCGGCCCCTCCTCCCCACATCTGCCCCGTGTCCAGAGGTCCAGAGGTGA CGGCCCCGCCCCCTCCTCGGCCCCTCCTCCCCCCATCTGCCCCGTGTCCAGAGGTCCAGAGGTGA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:14536941..14537160 26863196 MeRIP-seq:(Medium) rs1273587603 Functional Loss SNV dbSNP153 33..33 33 - - - 82170 RMVar_ID_82170 Human_SNP_ID_659366390 m1A Human chr19 - 14552857 14552857 14552857 ACTATGCTGAGACTGCCACCCAGGCCTCACCCAGGCCCTATAAGAAAAAGACTGGGCCGGGCGCA ACTATGCTGAGACTGCCACCCAGGCCTCACCCGGGCCCTATAAGAAAAAGACTGGGCCGGGCGCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14552853..14552992 26863196 MeRIP-seq:(Medium) rs939243950 Functional Loss SNV dbSNP153 33..33 33 - - - 82171 RMVar_ID_82171 Human_SNP_ID_659366398 m1A Human chr19 - 14552878 14552878 14552878 GATGCTCACCCTGTACCTAGGACTATGCTGAGACTGCCACCCAGGCCTCACCCAGGCCCTATAAG GATGCTCACCCTGTACCTAGGACTATGCTGAGGCTGCCACCCAGGCCTCACCCAGGCCCTATAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14552876..14553046 26863196 MeRIP-seq:(Medium) rs1368309684 Functional Loss SNV dbSNP153 33..33 33 - - - 82172 RMVar_ID_82172 Human_SNP_ID_659366620 m1A Human chr19 + 14553676 14553676 14553676 GAGGGCTGAGCCGCTGAGCCGGAGTCCAGATGAATGTGCCGGAGTCTCTGCATTTGTGATGGGGG GAGGGCTGAGCCGCTGAGCCGGAGTCCAGATGCATGTGCCGGAGTCTCTGCATTTGTGATGGGGG A C TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14553673..14553780 26863196 MeRIP-seq:(Medium) rs1000823536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196187,Human_RBP_ID_23784059 RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035 82173 RMVar_ID_82173 Human_SNP_ID_659369864 m1A Human chr19 - 14564184 14564162 14564185 TGATGTAGTGGAATGAGTGACAGATGCAGGCGAGGCTGGTCGGGGGGAGCAGGCTCAGCTGGGGC TGATGTAGTGGAATGAGTGACAGATGCAGGC_______________________TCAGCTGGGGC AGCCTGCTCCCCCCGACCAGCCTC A lnc-NDUFB7-1 RNACentral:URS0000D57FE3 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:14564176..14564275 32194978 MeRIP-seq:(Medium) rs1568431000 Functional Loss DEL dbSNP153 32..54 33 - - - 82174 RMVar_ID_82174 Human_SNP_ID_659369892 m1A Human chr19 + 14564203 14564203 14564203 CCCCCGACCAGCCTCGCCTGCATCTGTCACTCATTCCACTACATCAAGCGCCTGCTGGAGACGCT CCCCCGACCAGCCTCGCCTGCATCTGTCACTCCTTCCACTACATCAAGCGCCTGCTGGAGACGCT A C TECR Ensembl:ENSG00000099797 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:14564051..14564352 26863196 MeRIP-seq:(Medium) rs751580386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52932,Human_RBP_ID_514447,Human_RBP_ID_1013359,Human_RBP_ID_17266846,Human_RBP_ID_17382229,Human_RBP_ID_17497980,Human_RBP_ID_17915978,Human_RBP_ID_18192069,Human_RBP_ID_22422460,Human_RBP_ID_22446520,Human_RBP_ID_22501781,Human_RBP_ID_22763899,Human_RBP_ID_26815431,Human_RBP_ID_27464267 Human_Splice_Rec_1968996,Human_Splice_Rec_1968997,Human_Splice_Rec_1969012,Human_Splice_Rec_1969013,Human_Splice_Rec_1969036,Human_Splice_Rec_1969037,Human_Splice_Rec_1969060,Human_Splice_Rec_1969061,Human_Splice_Rec_1969086,Human_Splice_Rec_1969087,Human_Splice_Rec_1969113,Human_Splice_Rec_1969136,Human_Splice_Rec_1969137,Human_Splice_Rec_1969158,Human_Splice_Rec_1969159,Human_Splice_Rec_1969172,Human_Splice_Rec_1969173,Human_Splice_Rec_1969220,Human_Splice_Rec_1969221,Human_Splice_Rec_1969236,Human_Splice_Rec_1969237,Human_Splice_Rec_1969248,Human_Splice_Rec_1969249,Human_Splice_Rec_1969261,Human_Splice_Rec_1969271,Human_Splice_Rec_1969281 RMVar_hsa_circ_1359,RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035,RMVar_hsa_circ_114292,RMVar_hsa_circ_7258,RMVar_hsa_circ_193038,RMVar_hsa_circ_372271,RMVar_hsa_circ_340628,RMVar_hsa_circ_304683,RMVar_hsa_circ_193040,RMVar_hsa_circ_193041,RMVar_hsa_circ_193039 82175 RMVar_ID_82175 Human_SNP_ID_659369920 m1A Human chr19 + 14564256 14564256 14564256 GCTGGAGACGCTCTTCGTGCACCGCTTCTCCCATGGCACTATGCCTTTGCGCAACATCTTCAAGG GCTGGAGACGCTCTTCGTGCACCGCTTCTCCCTTGGCACTATGCCTTTGCGCAACATCTTCAAGG A T TECR Ensembl:ENSG00000099797 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:14564072..14564336 26863196 MeRIP-seq:(Medium) rs1356949234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52933,Human_RBP_ID_514447,Human_RBP_ID_17266849,Human_RBP_ID_18192069,Human_RBP_ID_22763900,Human_RBP_ID_26815431 Human_Splice_Rec_1968996,Human_Splice_Rec_1968997,Human_Splice_Rec_1969012,Human_Splice_Rec_1969013,Human_Splice_Rec_1969036,Human_Splice_Rec_1969037,Human_Splice_Rec_1969060,Human_Splice_Rec_1969061,Human_Splice_Rec_1969086,Human_Splice_Rec_1969087,Human_Splice_Rec_1969113,Human_Splice_Rec_1969136,Human_Splice_Rec_1969137,Human_Splice_Rec_1969158,Human_Splice_Rec_1969159,Human_Splice_Rec_1969172,Human_Splice_Rec_1969173,Human_Splice_Rec_1969220,Human_Splice_Rec_1969221,Human_Splice_Rec_1969236,Human_Splice_Rec_1969237,Human_Splice_Rec_1969248,Human_Splice_Rec_1969249,Human_Splice_Rec_1969261,Human_Splice_Rec_1969271,Human_Splice_Rec_1969281 RMVar_hsa_circ_1359,RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035,RMVar_hsa_circ_114292,RMVar_hsa_circ_7258,RMVar_hsa_circ_193038,RMVar_hsa_circ_372271,RMVar_hsa_circ_340628,RMVar_hsa_circ_304683,RMVar_hsa_circ_193040,RMVar_hsa_circ_193041,RMVar_hsa_circ_193039 82176 RMVar_ID_82176 Human_SNP_ID_659369939 m1A Human chr19 - 14564289 14564289 14564289 GGGGCTTAGGGGTGAGGCGGGGACGGGCTCTCACCTTGAAGATGTTGCGCAAAGGCATAGTGCCA GGGGCTTAGGGGTGAGGCGGGGACGGGCTCTCGCCTTGAAGATGTTGCGCAAAGGCATAGTGCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14564246..14564753 32194978 MeRIP-seq:(Medium) rs113641320 Functional Loss SNV dbSNP153 33..33 33 - - - 82177 RMVar_ID_82177 Human_SNP_ID_659370166 m1A Human chr19 + 14564671 14564671 14564671 TTGGCCCCGCCTATCCTCCCCAGCCCCGCCCCAAGGCCCCTCCTGTCCTTTCCCACCATGCTCCC TTGGCCCCGCCTATCCTCCCCAGCCCCGCCCCCAGGCCCCTCCTGTCCTTTCCCACCATGCTCCC A C TECR Ensembl:ENSG00000099797 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:14564668..14564900 26863196 MeRIP-seq:(Medium) rs1366840702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130290,Human_RBP_ID_17081739 RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035,RMVar_hsa_circ_114292,RMVar_hsa_circ_193038,RMVar_hsa_circ_372271,RMVar_hsa_circ_340628,RMVar_hsa_circ_193040,RMVar_hsa_circ_193039 82178 RMVar_ID_82178 Human_SNP_ID_659370876 m1A Human chr19 - 14566239 14566239 14566239 CCCCAGCTATGTGATGCGCATGAAGGAGTTTGAGCGGGAGCGGAGGCTGCTCCAGCGGAAGAAGC CCCCAGCTATGTGATGCGCATGAAGGAGTTTGCGCGGGAGCGGAGGCTGCTCCAGCGGAAGAAGC T G NDUFB7 Ensembl:ENSG00000099795 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:14566131..14566308;chr19:14566151..14566300 26863196 MeRIP-seq:(Medium) rs145776636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514452,Human_RBP_ID_1555604,Human_RBP_ID_1880586,Human_RBP_ID_3563740,Human_RBP_ID_5116138,Human_RBP_ID_17655993,Human_RBP_ID_17935270,Human_RBP_ID_18723470,Human_RBP_ID_23784071,Human_RBP_ID_26817147 Human_Splice_Rec_1969318,Human_Splice_Rec_1969322 Human_miRNA_ID_2517692 RMVar_hsa_circ_81357,RMVar_hsa_circ_193049 82179 RMVar_ID_82179 Human_SNP_ID_659370881 m1A Human chr19 - 14566252 14566252 14566252 TCTCGTGCTTTTCCCCCAGCTATGTGATGCGCATGAAGGAGTTTGAGCGGGAGCGGAGGCTGCTC TCTCGTGCTTTTCCCCCAGCTATGTGATGCGCTTGAAGGAGTTTGAGCGGGAGCGGAGGCTGCTC T A NDUFB7 Ensembl:ENSG00000099795 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:14566201..14566275 32194978 MeRIP-seq:(Medium) rs768959190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514452,Human_RBP_ID_1555604,Human_RBP_ID_1880586,Human_RBP_ID_3563740,Human_RBP_ID_4562890,Human_RBP_ID_17935270,Human_RBP_ID_18723470,Human_RBP_ID_23784071,Human_RBP_ID_25386433,Human_RBP_ID_26815432 Human_Splice_Rec_1969318,Human_Splice_Rec_1969322 Human_miRNA_ID_2196186,Human_miRNA_ID_2517692 RMVar_hsa_circ_81357,RMVar_hsa_circ_193049 82180 RMVar_ID_82180 Human_SNP_ID_659371350 m1A Human chr19 - 14567557 14567557 14567557 GCCCCCTCCTGAAGGTTGATTTGTCCGGAGTCAGGTTTGCTAGGTGAGTGGGGCACCGGGACCCA GCCCCCTCCTGAAGGTTGATTTGTCCGGAGTCGGGTTTGCTAGGTGAGTGGGGCACCGGGACCCA T C NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:14567553..14568075 26863196 MeRIP-seq:(Medium) rs1238695120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13378420,Human_RBP_ID_22501785 82181 RMVar_ID_82181 Human_SNP_ID_659371561 m1A Human chr19 - 14568345 14568345 14568345 CATACGGGGCGGCAGCAGAGAAAAAGGCTCTCAGGCCGGGCACAGTGGCTCACACCTGTAATCCC CATACGGGGCGGCAGCAGAGAAAAAGGCTCTCGGGCCGGGCACAGTGGCTCACACCTGTAATCCC T C NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14568337..14568506 26863196 MeRIP-seq:(Medium) rs1032031659 Functional Loss SNV dbSNP153 33..33 33 - - - 82182 RMVar_ID_82182 Human_SNP_ID_659371765 m1A Human chr19 + 14569107 14569107 14569107 TGAGGCGGGAGAATCGCTTGAACCGGGAAGGCAGATGTTGCAGTGAGCAAAGTGACTGGCTGAAA TGAGGCGGGAGAATCGCTTGAACCGGGAAGGCGGATGTTGCAGTGAGCAAAGTGACTGGCTGAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:14569105..14569233 26863196 MeRIP-seq:(Medium) rs1265484593 Functional Loss SNV dbSNP153 33..33 33 - - - 82183 RMVar_ID_82183 Human_SNP_ID_659371869 m1A Human chr19 + 14569534 14569534 14569534 CGGGGATAGGCACCAAGGAAGGGAAAGAGGTGAGTTTATCCAGAGTAAGCAAGAGAGAAGGGCAG CGGGGATAGGCACCAAGGAAGGGAAAGAGGTGGGTTTATCCAGAGTAAGCAAGAGAGAAGGGCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14569532..14569792 26863196 MeRIP-seq:(Medium) rs1447863732 Functional Loss SNV dbSNP153 33..33 33 - - - 82184 RMVar_ID_82184 Human_SNP_ID_659372555 m1A Human chr19 - 14571990 14571990 14571990 GGGATCTGCAGCGACTGCAGCCATGGGGGCCCACCTGGTCCGGCGCTACCTGGGCGATGCCTCGG GGGATCTGCAGCGACTGCAGCCATGGGGGCCCCCCTGGTCCGGCGCTACCTGGGCGATGCCTCGG T G NDUFB7 Ensembl:ENSG00000099795 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14571876..14572075 26863410 MeRIP-seq:(Medium) rs1312574024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1013365,Human_RBP_ID_4557284,Human_RBP_ID_5116759,Human_RBP_ID_5145094,Human_RBP_ID_5320221,Human_RBP_ID_5421212,Human_RBP_ID_8839851,Human_RBP_ID_9328721,Human_RBP_ID_22501788 82185 RMVar_ID_82185 Human_SNP_ID_659372573 m1A Human chr19 - 14572013 14572013 14572013 CTAGGTGACCCTCGGCTGCTGCAGGGATCTGCAGCGACTGCAGCCATGGGGGCCCACCTGGTCCG CTAGGTGACCCTCGGCTGCTGCAGGGATCTGCCGCGACTGCAGCCATGGGGGCCCACCTGGTCCG T G NDUFB7 Ensembl:ENSG00000099795 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr19:14571876..14572025;chr19:14571901..14572075;chr19:14571838..14572075 26863196 MeRIP-seq:(Medium) rs766937528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557285,Human_RBP_ID_5116759,Human_RBP_ID_5145094,Human_RBP_ID_5320221,Human_RBP_ID_9084733,Human_RBP_ID_9328721,Human_RBP_ID_18421645 82186 RMVar_ID_82186 Human_SNP_ID_659372580 m1A Human chr19 - 14572023 14572023 14572023 CGGGTAGGAGCTAGGTGACCCTCGGCTGCTGCAGGGATCTGCAGCGACTGCAGCCATGGGGGCCC CGGGTAGGAGCTAGGTGACCCTCGGCTGCTGCGGGGATCTGCAGCGACTGCAGCCATGGGGGCCC T C NDUFB7 Ensembl:ENSG00000099795 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:14571822..14572075;chr19:14571830..14572075 26863196 MeRIP-seq:(Medium) rs762531992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514460,Human_RBP_ID_4557285,Human_RBP_ID_5145094,Human_RBP_ID_5468321,Human_RBP_ID_8478362,Human_RBP_ID_8829992,Human_RBP_ID_9084733,Human_RBP_ID_18421645 82187 RMVar_ID_82187 Human_SNP_ID_659372581 m1A Human chr19 - 14572023 14572023 14572023 CGGGTAGGAGCTAGGTGACCCTCGGCTGCTGCAGGGATCTGCAGCGACTGCAGCCATGGGGGCCC CGGGTAGGAGCTAGGTGACCCTCGGCTGCTGCCGGGATCTGCAGCGACTGCAGCCATGGGGGCCC T G NDUFB7 Ensembl:ENSG00000099795 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:14571822..14572075;chr19:14571830..14572075 26863196 MeRIP-seq:(Medium) rs762531992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514460,Human_RBP_ID_4557285,Human_RBP_ID_5145094,Human_RBP_ID_5468321,Human_RBP_ID_8478362,Human_RBP_ID_8829992,Human_RBP_ID_9084733,Human_RBP_ID_18421645 82188 RMVar_ID_82188 Human_SNP_ID_659405103 m1A Human chr19 + 14690116 14690096 14690116 GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCACGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GAGCTGTGCTGCG____________________CGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GCGGCGCGGCGCGGTGCGGCA G ZNF333 Ensembl:ENSG00000160961 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14690050..14690135 26863410 MeRIP-seq:(Medium) rs1224485890 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_279252 Human_Splice_Rec_1969541,Human_Splice_Rec_1969563,Human_Splice_Rec_1969581,Human_Splice_Rec_1969589,Human_Splice_Rec_1969611,Human_Splice_Rec_1969623,Human_Splice_Rec_1969633 82189 RMVar_ID_82189 Human_SNP_ID_659405110 m1A Human chr19 + 14690116 14690101 14690116 GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCACGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GAGCTGTGCTGCGCGGCG_______________CGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GCGGCGCGGTGCGGCA G ZNF333 Ensembl:ENSG00000160961 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14690050..14690135 26863410 MeRIP-seq:(Medium) rs1437257272 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_279252 Human_Splice_Rec_1969541,Human_Splice_Rec_1969563,Human_Splice_Rec_1969581,Human_Splice_Rec_1969589,Human_Splice_Rec_1969611,Human_Splice_Rec_1969623,Human_Splice_Rec_1969633 82190 RMVar_ID_82190 Human_SNP_ID_659405133 m1A Human chr19 + 14690116 14690116 14690116 GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCACGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCCCGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC A C ZNF333 Ensembl:ENSG00000160961 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14690050..14690135 26863410 MeRIP-seq:(Medium) rs892545891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279252 Human_Splice_Rec_1969541,Human_Splice_Rec_1969563,Human_Splice_Rec_1969581,Human_Splice_Rec_1969589,Human_Splice_Rec_1969611,Human_Splice_Rec_1969623,Human_Splice_Rec_1969633 82191 RMVar_ID_82191 Human_SNP_ID_659405134 m1A Human chr19 + 14690116 14690116 14690116 GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCACGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC GAGCTGTGCTGCGCGGCGCGGCGCGGTGCGGCGCGGCACGGTGGGAGTGTCTCCGGCTGGCTTGC A G ZNF333 Ensembl:ENSG00000160961 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:14690050..14690135 26863410 MeRIP-seq:(Medium) rs892545891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279252 Human_Splice_Rec_1969541,Human_Splice_Rec_1969563,Human_Splice_Rec_1969581,Human_Splice_Rec_1969589,Human_Splice_Rec_1969611,Human_Splice_Rec_1969623,Human_Splice_Rec_1969633 82192 RMVar_ID_82192 Human_SNP_ID_659405150 m1A Human chr19 - 14690145 14690145 14690145 CCGCCCTCCCGAGGGGCCGGGCCACACCTGCAAGCCAGCCGGAGACACTCCCACCGTGCCGTGCC CCGCCCTCCCGAGGGGCCGGGCCACACCTGCAGGCCAGCCGGAGACACTCCCACCGTGCCGTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14690106..14690216 26863196 MeRIP-seq:(Medium) rs4808305 Functional Loss SNV dbSNP153 33..33 33 - - - 82193 RMVar_ID_82193 Human_SNP_ID_659410945 m1A Human chr19 - 14711973 14711973 14711973 TTTCTTTTTGGATCCACTGAAACGTCGCCCTCAGAGTGCCCCATCCTGAGGTCTCCTCCCCTGTA TTTCTTTTTGGATCCACTGAAACGTCGCCCTCGGAGTGCCCCATCCTGAGGTCTCCTCCCCTGTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14711931..14712125 26863196 MeRIP-seq:(Medium) rs997850403 Functional Loss SNV dbSNP153 33..33 33 - - - 82194 RMVar_ID_82194 Human_SNP_ID_659424305 m1A Human chr19 - 14763846 14763836 14763847 CGGGAGGAGGAGGACAGGATGGGGAGGAGAGGAGGAGGAGAGAAGGAGGAGGAGAGGAGGAAGAG CGGGAGGAGGAGGACAGGATGGGGAGGAGAG___________AAGGAGGAGGAGAGGAGGAAGAG TCTCTCCTCCTC T ADGRE2 Ensembl:ENSG00000127507 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14763679..14763845 26863196 MeRIP-seq:(Medium) rs1184054854 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_5191352 RMVar_hsa_circ_113061,RMVar_hsa_circ_193065 82195 RMVar_ID_82195 Human_SNP_ID_707276790 m1A Human chrX + 13745 13745 13745 GGGACCACCCCCAGACCCCCGCTCCTCCCCTCAGGACCACCCCCAGATCCACTGTTCCTGTCCTC GGGACCACCCCCAGACCCCCGCTCCTCCCCTCCGGACCACCCCCAGATCCACTGTTCCTGTCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:13700..13772 26863196 MeRIP-seq:(Medium) rs368125700 Functional Loss SNV dbSNP153 33..33 33 - - - 82196 RMVar_ID_82196 Human_SNP_ID_707276791 m1A Human chrX + 13745 13745 13745 GGGACCACCCCCAGACCCCCGCTCCTCCCCTCAGGACCACCCCCAGATCCACTGTTCCTGTCCTC GGGACCACCCCCAGACCCCCGCTCCTCCCCTCGGGACCACCCCCAGATCCACTGTTCCTGTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:13700..13772 26863196 MeRIP-seq:(Medium) rs368125700 Functional Loss SNV dbSNP153 33..33 33 - - - 82197 RMVar_ID_82197 Human_SNP_ID_707331546 m1A Human chrX - 276953 276953 276953 CCCAGACGCCCGGTGACCCGCCAGGCGGGGTGAGACACCTACACCTTCCCGCCCGCTGAGTCCTC CCCAGACGCCCGGTGACCCGCCAGGCGGGGTGGGACACCTACACCTTCCCGCCCGCTGAGTCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:276950..277051 26863196 MeRIP-seq:(Medium) rs1418179690 Functional Loss SNV dbSNP153 33..33 33 - - - 82198 RMVar_ID_82198 Human_SNP_ID_707331938 m1A Human chrX + 277974 277974 277974 ACGTGGGGACAGGTGTGGGGATAGGAGGGGACACCCCTCAGTGGTCAGGGGACCTGGGATGTGAG ACGTGGGGACAGGTGTGGGGATAGGAGGGGACCCCCCTCAGTGGTCAGGGGACCTGGGATGTGAG A C PLCXD1 Ensembl:ENSG00000182378 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:277924..278191 26863196 MeRIP-seq:(Medium) rs1448648788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8226404 82199 RMVar_ID_82199 Human_SNP_ID_707331959 m1A Human chrX - 278037 278037 278037 GACCACTGAGGGGTGTCCGCTCCTATCCCCACACCTGTCCCCACATTCCCCCTGACCCCTCCCCT GACCACTGAGGGGTGTCCGCTCCTATCCCCACGCCTGTCCCCACATTCCCCCTGACCCCTCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:278034..278122 26863196 MeRIP-seq:(Medium) rs1361363128 Functional Loss SNV dbSNP153 33..33 33 - - - 82200 RMVar_ID_82200 Human_SNP_ID_707332836 m1A Human chrX + 280379 280379 280379 CAGGGGGAAGGGGGGCCGTGCAGGGGGAAGGGAGGCCGTGCAGGGGGAAGGGAGGCCGTGCAGGC CAGGGGGAAGGGGGGCCGTGCAGGGGGAAGGGGGGCCGTGCAGGGGGAAGGGAGGCCGTGCAGGC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:280378..280443 26863196 MeRIP-seq:(Medium) rs866151809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16289,Human_RBP_ID_3930497,Human_RBP_ID_8226409,Human_RBP_ID_9443097,Human_RBP_ID_18468276,Human_RBP_ID_18963344,Human_RBP_ID_24555710,Human_RBP_ID_26797203 82201 RMVar_ID_82201 Human_SNP_ID_707332856 m1A Human chrX + 280414 280409 280414 CCGTGCAGGGGGAAGGGAGGCCGTGCAGGCAGAGGGGAAGACGTGCAGGGGGAGGGGAGGCCGTG CCGTGCAGGGGGAAGGGAGGCCGTGCAG_____GGGGAAGACGTGCAGGGGGAGGGGAGGCCGTG GGCAGA G PLCXD1 Ensembl:ENSG00000182378 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:280374..280457 26863196 MeRIP-seq:(Medium) rs1387256769 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_3930497,Human_RBP_ID_8226409,Human_RBP_ID_9443097,Human_RBP_ID_18468276,Human_RBP_ID_18963344,Human_RBP_ID_22734376,Human_RBP_ID_24555710,Human_RBP_ID_26797203 82202 RMVar_ID_82202 Human_SNP_ID_707334263 m1A Human chrX - 283609 283609 283609 CCCCACCCGGGCCTGGCAACACGGCCGCCCCCACCCGGGCCTGGCACCACGGCCGCCCCCACCCG CCCCACCCGGGCCTGGCAACACGGCCGCCCCCCCCCGGGCCTGGCACCACGGCCGCCCCCACCCG T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrX:283538..283622 26863410 MeRIP-seq:(Medium) rs1252724944 Functional Loss SNV dbSNP153 33..33 33 - - - 82203 RMVar_ID_82203 Human_SNP_ID_707334286 m1A Human chrX - 283637 283637 283637 CCCCACCCGGGCCTGACACCAAGGCCGCCCCCACCCGGGCCTGGCAACACGGCCGCCCCCACCCG CCCCACCCGGGCCTGACACCAAGGCCGCCCCCCCCCGGGCCTGGCAACACGGCCGCCCCCACCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:283635..283865 26863196 MeRIP-seq:(Medium) rs1471756767 Functional Loss SNV dbSNP153 33..33 33 - - - 82204 RMVar_ID_82204 Human_SNP_ID_707334569 m1A Human chrX - 284303 284303 284303 CCTGCCCCACCCCAACCTCACCTGGGATGGAGAGGTGGTGGAGGGGCACATCCCAGAGCCGGGGA CCTGCCCCACCCCAACCTCACCTGGGATGGAGCGGTGGTGGAGGGGCACATCCCAGAGCCGGGGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:284253..290700 32194978 MeRIP-seq:(Medium) rs1569564402 Functional Loss SNV dbSNP153 33..33 33 - - - 82205 RMVar_ID_82205 Human_SNP_ID_707336476 m1A Human chrX + 288787 288787 288787 CTGCCTGAACAAGAAGTCCCCCATTTCGCACGAGGAGTCCCGGCTGCTGCAGCTGCTGAACAAGG CTGCCTGAACAAGAAGTCCCCCATTTCGCACGCGGAGTCCCGGCTGCTGCAGCTGCTGAACAAGG A C PLCXD1 Ensembl:ENSG00000182378 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:288689..288827 26863196 MeRIP-seq:(Medium) rs1193899853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1405381,Human_RBP_ID_7992538,Human_RBP_ID_9409618,Human_RBP_ID_19027027 Human_Splice_Rec_2182378,Human_Splice_Rec_2182379,Human_Splice_Rec_2182385,Human_Splice_Rec_2182393,Human_Splice_Rec_2182402,Human_Splice_Rec_2182410,Human_Splice_Rec_2182412,Human_Splice_Rec_2182413,Human_Splice_Rec_2182417 RMVar_hsa_circ_28257,RMVar_hsa_circ_289750,RMVar_hsa_circ_344677,RMVar_hsa_circ_273785,RMVar_hsa_circ_261159,RMVar_hsa_circ_261160 82206 RMVar_ID_82206 Human_SNP_ID_707337326 m1A Human chrX - 290736 290736 290736 GCGCCGTTGTGTACACCATATGGACAAAGTGCAGGTTCTTCTCCGAGCCCTCCAGCATGTGGGCT GCGCCGTTGTGTACACCATATGGACAAAGTGCCGGTTCTTCTCCGAGCCCTCCAGCATGTGGGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:290597..290828 26863196 MeRIP-seq:(Medium) rs1221719779 Functional Loss SNV dbSNP153 33..33 33 - - - 82207 RMVar_ID_82207 Human_SNP_ID_707340822 m1A Human chrX - 299118 299118 299118 CCAGAACGTACTGCAGGTTCTCCGTGAGGTTGATGCCGGCCACGAACAACCCTCCTGCAACGGTG CCAGAACGTACTGCAGGTTCTCCGTGAGGTTGGTGCCGGCCACGAACAACCCTCCTGCAACGGTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:299112..299412 32194978 MeRIP-seq:(Medium) rs1472987711 Functional Loss SNV dbSNP153 33..33 33 - - - 82208 RMVar_ID_82208 Human_SNP_ID_707341879 m1A Human chrX + 301090 301090 301090 TGGAGGGCAGTGGTACAGTCATAGCTCACTGCAGCCTCAACCTCCTGGGCTCAAGCGATCCTCTC TGGAGGGCAGTGGTACAGTCATAGCTCACTGCCGCCTCAACCTCCTGGGCTCAAGCGATCCTCTC A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1195763832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1398227 82209 RMVar_ID_82209 Human_SNP_ID_707341899 m1A Human chrX + 301185 301185 301185 GGGACACACCCCCACTGCTGGCTAATTTTTGTATTTTTGGTAGAGTCAGGGTTTCACCACATGGC GGGACACACCCCCACTGCTGGCTAATTTTTGTGTTTTTGGTAGAGTCAGGGTTTCACCACATGGC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1215688990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16961368 82210 RMVar_ID_82210 Human_SNP_ID_707342072 m1A Human chrX + 301729 301729 301729 CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCCATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs374073214 Functional Loss SNV dbSNP153 33..33 33 - - - 82211 RMVar_ID_82211 Human_SNP_ID_707342073 m1A Human chrX + 301729 301729 301729 CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs374073214 Functional Loss SNV dbSNP153 33..33 33 - - - 82212 RMVar_ID_82212 Human_SNP_ID_707343395 m1A Human chrX + 305076 305076 305076 CCCACCCCGCAGGCCTCTGTGGGCGTCCGTTCATCCTGGAAAGAGCTTCCGGAATTTGCCGTAGG CCCACCCCGCAGGCCTCTGTGGGCGTCCGTTCGTCCTGGAAAGAGCTTCCGGAATTTGCCGTAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:305026..305197 26863196 MeRIP-seq:(Medium) rs371491296 Functional Loss SNV dbSNP153 33..33 33 - - - 82213 RMVar_ID_82213 Human_SNP_ID_707343406 m1A Human chrX - 305098 305098 305098 AGGGTCATCATCAGCAACTCAGCCTACGGCAAATTCCGGAAGCTCTTTCCAGGATGAACGGACGC AGGGTCATCATCAGCAACTCAGCCTACGGCAAGTTCCGGAAGCTCTTTCCAGGATGAACGGACGC T C GTPBP6 Ensembl:ENSG00000178605 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:305053..305137 26863196 MeRIP-seq:(Medium) rs1280390837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17325901,Human_RBP_ID_18149132,Human_RBP_ID_18918384 82214 RMVar_ID_82214 Human_SNP_ID_707344521 m1A Human chrX - 307335 307335 307335 CAGCTCAGGTGAGCGGCCTGCAGGGGCAGGAGACGGGATGGTGCTTTGGATGCCTGTCTCTGGCT CAGCTCAGGTGAGCGGCCTGCAGGGGCAGGAGGCGGGATGGTGCTTTGGATGCCTGTCTCTGGCT T C GTPBP6 Ensembl:ENSG00000178605 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:307330..307413 26863196 MeRIP-seq:(Medium) rs770925943 Functional Loss SNV dbSNP153 33..33 33 - - - 82215 RMVar_ID_82215 Human_SNP_ID_707346311 m1A Human chrX - 311517 311517 311517 TCACGGCCCACGCGGGCACGCTGCCCTCACGCATGACCGTCCTGTACGTGGACACCATCGGCTTC TCACGGCCCACGCGGGCACGCTGCCCTCACGCGTGACCGTCCTGTACGTGGACACCATCGGCTTC T C GTPBP6 Ensembl:ENSG00000178605 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:311466..311585 26863196 MeRIP-seq:(Medium) rs761381735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1405396,Human_RBP_ID_22123071 Human_Splice_Rec_2182419 82216 RMVar_ID_82216 Human_SNP_ID_707346520 m1A Human chrX + 311855 311855 311855 GATGGAGCGGGGCCGCCGTGCGGACACGGGGGAGATGGTGGTGTGGACGGGTGTGCGTGTGAAGG GATGGAGCGGGGCCGCCGTGCGGACACGGGGGGGATGGTGGTGTGGACGGGTGTGCGTGTGAAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:311851..312220 26863196 MeRIP-seq:(Medium) rs935556883 Functional Loss SNV dbSNP153 33..33 33 - - - 82217 RMVar_ID_82217 Human_SNP_ID_707346521 m1A Human chrX + 311855 311855 311855 GATGGAGCGGGGCCGCCGTGCGGACACGGGGGAGATGGTGGTGTGGACGGGTGTGCGTGTGAAGG GATGGAGCGGGGCCGCCGTGCGGACACGGGGGTGATGGTGGTGTGGACGGGTGTGCGTGTGAAGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:311851..312220 26863196 MeRIP-seq:(Medium) rs935556883 Functional Loss SNV dbSNP153 33..33 33 - - - 82218 RMVar_ID_82218 Human_SNP_ID_707346727 m1A Human chrX + 312305 312214 312306 AACATTGTGGTGTACACGGGTGGATTATGTAGACGGGGTGGTGGTATAGATGGGGTAGTGGTGCT __________________________________GGGGTGGTGGTATAGATGGGGTAGTGGTGCT TGGTGGTATAGCTGGGGCAGTGGTGCCAGTGTAGACAGGAGGACGGTGCAGACAAAGGGAACATTGTGGTGTACACGGGTGGATTATGTAGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:312303..312436 26863196 MeRIP-seq:(Medium) rs1569351386 Functional Loss DEL dbSNP153 1..34 33 - - - 82219 RMVar_ID_82219 Human_SNP_ID_707349982 m1A Human chrX - 318186 318186 318186 CGGGACTCGGGAGAATCATAGCTGGCGATGCAAGGGCGGGGCTCTGGGGAGGCTCATAGGTAGAG CGGGACTCGGGAGAATCATAGCTGGCGATGCATGGGCGGGGCTCTGGGGAGGCTCATAGGTAGAG T A GTPBP6 Ensembl:ENSG00000178605 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:318179..318293 26863196 MeRIP-seq:(Medium) rs1215731816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930509,Human_RBP_ID_8226423,Human_RBP_ID_21997213 82220 RMVar_ID_82220 Human_SNP_ID_707350148 m1A Human chrX - 318582 318582 318582 GGCGGACGGCGGCCGAAGCCGCACGGGAGACGACGAGGAGGAGCCGGAAGATGCGGACGAGAACG GGCGGACGGCGGCCGAAGCCGCACGGGAGACGGCGAGGAGGAGCCGGAAGATGCGGACGAGAACG T C GTPBP6 Ensembl:ENSG00000178605 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:318531..318675 26863196 MeRIP-seq:(Medium) rs1230995323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076445,Human_RBP_ID_5411646,Human_RBP_ID_9339856,Human_RBP_ID_9443613,Human_RBP_ID_19027048,Human_RBP_ID_23107621,Human_RBP_ID_26362630 82221 RMVar_ID_82221 Human_SNP_ID_707354266 m1A Human chrX + 327813 327812 327813 GGGGACATGTGACCCCAGCGAGGTGGTCGGGGAGTCGTCGCCGGCCAGCGCTGCAGCCCAGGGAT GGGGACATGTGACCCCAGCGAGGTGGTCGGGG_GTCGTCGCCGGCCAGCGCTGCAGCCCAGGGAT GA G lnc-PLCXD1-2 RNACentral:URS00008C10BA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:327617..327869 26863196 MeRIP-seq:(Medium) rs1432091102 Functional Loss DEL dbSNP153 33..33 33 - - - 82222 RMVar_ID_82222 Human_SNP_ID_707354291 m1A Human chrX - 327848 327848 327848 CTGTGCTCCACAACCAAACTCCTAGAGCCGTCATCATCCCTGGGCTGCAGCGCTGGCCGGCGACG CTGTGCTCCACAACCAAACTCCTAGAGCCGTCGTCATCCCTGGGCTGCAGCGCTGGCCGGCGACG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:327697..328117 32194978 MeRIP-seq:(Medium) rs185257159 Functional Loss SNV dbSNP153 33..33 33 - - - 82223 RMVar_ID_82223 Human_SNP_ID_707354365 m1A Human chrX - 328015 328015 328015 AGAGGGAGCCAAGCCTCGGGGGCCCAGCCCGGATGCCGCCGACTCCCACCCGCCAGCCTCGCCGA AGAGGGAGCCAAGCCTCGGGGGCCCAGCCCGGCTGCCGCCGACTCCCACCCGCCAGCCTCGCCGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:327612..328205 26863196 MeRIP-seq:(Medium) rs1158667281 Functional Loss SNV dbSNP153 33..33 33 - - - 82224 RMVar_ID_82224 Human_SNP_ID_707354812 m1A Human chrX - 328745 328745 328745 AGGGGGGAGGGGGAGAGGGGAGGGGGGCGGGGAGGGGGGAGGGGGAGAGGGGAGGGGGACGGGGA AGGGGGGAGGGGGAGAGGGGAGGGGGGCGGGGGGGGGGGAGGGGGAGAGGGGAGGGGGACGGGGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:328726..328800 26863196 MeRIP-seq:(Medium) rs1438327609 Functional Loss SNV dbSNP153 33..33 33 - - - 82225 RMVar_ID_82225 Human_SNP_ID_707354820 m1A Human chrX - 328770 328770 328770 GCAGGGAGAGGGGAGGGGGGCGGGGAGGGGGGAGGGGGAGAGGGGAGGGGGGCGGGGAGGGGGGA GCAGGGAGAGGGGAGGGGGGCGGGGAGGGGGGGGGGGGAGAGGGGAGGGGGGCGGGGAGGGGGGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:328726..328800 26863196 MeRIP-seq:(Medium) rs1233148760 Functional Loss SNV dbSNP153 33..33 33 - - - 82226 RMVar_ID_82226 Human_SNP_ID_707354821 m1A Human chrX - 328777 328777 328777 GGGGAGGGCAGGGAGAGGGGAGGGGGGCGGGGAGGGGGGAGGGGGAGAGGGGAGGGGGGCGGGGA GGGGAGGGCAGGGAGAGGGGAGGGGGGCGGGGGGGGGGGAGGGGGAGAGGGGAGGGGGGCGGGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:328726..328800 26863196 MeRIP-seq:(Medium) rs1336895560 Functional Loss SNV dbSNP153 33..33 33 - - - 82227 RMVar_ID_82227 Human_SNP_ID_707355077 m1A Human chrX - 329429 329429 329429 GACGGATGGGGCCGCCAGGTAGGCGTGCGGCCAGGACCACCCAAGGACTCAAGGGAGAGATGGGA GACGGATGGGGCCGCCAGGTAGGCGTGCGGCCGGGACCACCCAAGGACTCAAGGGAGAGATGGGA T C MG828806 RNACentral:URS0000E0D310 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:329398..329520 26863196 MeRIP-seq:(Medium) rs753898881 Functional Loss SNV dbSNP153 33..33 33 - - - 82228 RMVar_ID_82228 Human_SNP_ID_707355100 m1A Human chrX - 329456 329455 329456 GGGCATCGGCTGTCCCTGCCCTGAAGGGACGGATGGGGCCGCCAGGTAGGCGTGCGGCCAGGACC GGGCATCGGCTGTCCCTGCCCTGAAGGGACGG_TGGGGCCGCCAGGTAGGCGTGCGGCCAGGACC AT A MG828806 RNACentral:URS0000E0D310 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:329416..329558 26863196 MeRIP-seq:(Medium) rs1334968284 Functional Loss DEL dbSNP153 33..33 33 - - - 82229 RMVar_ID_82229 Human_SNP_ID_707355101 m1A Human chrX - 329456 329456 329456 GGGCATCGGCTGTCCCTGCCCTGAAGGGACGGATGGGGCCGCCAGGTAGGCGTGCGGCCAGGACC GGGCATCGGCTGTCCCTGCCCTGAAGGGACGGCTGGGGCCGCCAGGTAGGCGTGCGGCCAGGACC T G MG828806 RNACentral:URS0000E0D310 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:329416..329558 26863196 MeRIP-seq:(Medium) rs1426641383 Functional Loss SNV dbSNP153 33..33 33 - - - 82230 RMVar_ID_82230 Human_SNP_ID_707355891 m1A Human chrX - 330858 330858 330858 CCGTCGGGGGGGACGACCCCAGTGGTGCAGGGATAGGAGGTCCCGCTTGGACAAGCCCCCCACAG CCGTCGGGGGGGACGACCCCAGTGGTGCAGGGCTAGGAGGTCCCGCTTGGACAAGCCCCCCACAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:330603..331048 26863196 MeRIP-seq:(Medium) rs961125445 Functional Loss SNV dbSNP153 33..33 33 - - - 82231 RMVar_ID_82231 Human_SNP_ID_707356548 m1A Human chrX - 331720 331720 331720 AGGGGAGTTGGGGGAGAACGGGCGGGCATCAGATGCAGGAATGAGGCAGAGCCAGACCCAGCCGC AGGGGAGTTGGGGGAGAACGGGCGGGCATCAGTTGCAGGAATGAGGCAGAGCCAGACCCAGCCGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:331651..331940 26863196 MeRIP-seq:(Medium) rs1168079520 Functional Loss SNV dbSNP153 33..33 33 - - - 82232 RMVar_ID_82232 Human_SNP_ID_707357072 m1A Human chrX + 332338 332337 332339 CTGTGGCTGGCACCTTTCATGGTCCTCCCGGAACAGAGCTCATGCTGCTGCTCCTGGGTGGACCC CTGTGGCTGGCACCTTTCATGGTCCTCCCGGA__AGAGCTCATGCTGCTGCTCCTGGGTGGACCC AAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:332304..332441 26863196 MeRIP-seq:(Medium) rs1569365646 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1714463 82233 RMVar_ID_82233 Human_SNP_ID_707357434 m1A Human chrX - 332786 332786 332786 CAAGTGCCCCGTCCTTCCCCAGCCACAACCCCAGATGCCCCGGGCAGTGCCGGGGCCGGGCGTGC CAAGTGCCCCGTCCTTCCCCAGCCACAACCCCGGATGCCCCGGGCAGTGCCGGGGCCGGGCGTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:332299..333328 26863196 MeRIP-seq:(Medium) rs983749924 Functional Loss SNV dbSNP153 33..33 33 - - - 82234 RMVar_ID_82234 Human_SNP_ID_707357491 m1A Human chrX + 332848 332848 332848 TTGGGGGAATGCATTGGGTACAGGGATGTCGGAGGATGCTCAGTGGCTGTGCAGGGGCCTCACCA TTGGGGGAATGCATTGGGTACAGGGATGTCGGTGGATGCTCAGTGGCTGTGCAGGGGCCTCACCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:332800..332908 26863196 MeRIP-seq:(Medium) rs1272894709 Functional Loss SNV dbSNP153 33..33 33 - - - 82235 RMVar_ID_82235 Human_SNP_ID_707357532 m1A Human chrX + 332909 332909 332909 ACCAGCGTCGTGGGTGGGGGACGCTGTCTTTCACGGCCCCAGGGAGGCCTCTCATGTCTCAGCCT ACCAGCGTCGTGGGTGGGGGACGCTGTCTTTCGCGGCCCCAGGGAGGCCTCTCATGTCTCAGCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:332862..332966 32194978 MeRIP-seq:(Medium) rs1039800207 Functional Loss SNV dbSNP153 33..33 33 - - - 82236 RMVar_ID_82236 Human_SNP_ID_707357791 m1A Human chrX - 333188 333188 333188 TGGGTCTGCGAAGGGTCAGGACCCCCAACAACAGGACAGGTGCAGGGCAGGAGGTTCTGCCGCAG TGGGTCTGCGAAGGGTCAGGACCCCCAACAACGGGACAGGTGCAGGGCAGGAGGTTCTGCCGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:333138..333292 32194978 MeRIP-seq:(Medium) rs1187144821 Functional Loss SNV dbSNP153 33..33 33 - - - 82237 RMVar_ID_82237 Human_SNP_ID_707357933 m1A Human chrX - 333427 333427 333427 CGGCAGGGCAGGGCCAAGCCGGGACCACCCCGAGAGCAGCATACGCACCCCGTTCATCCACCGGC CGGCAGGGCAGGGCCAAGCCGGGACCACCCCGGGAGCAGCATACGCACCCCGTTCATCCACCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:333379..333559 26863196 MeRIP-seq:(Medium) rs1406317926 Functional Loss SNV dbSNP153 33..33 33 - - - 82238 RMVar_ID_82238 Human_SNP_ID_707358614 m1A Human chrX - 334377 334340 334377 GTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACGCCGCCCGCGAGAACGCCGCC GTACGAGTACGCATGCGGGGACGAGGACCTGG_________________________________ CCCGCGGCGGCGTTCTCGCGGGCGGCGTCACAGCGGCT C PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:334326..334429 26863196 MeRIP-seq:(Medium) rs768486103 Functional Loss DEL dbSNP153 33..65 33 - - - 82239 RMVar_ID_82239 Human_SNP_ID_707358667 m1A Human chrX - 334377 334377 334377 GTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACGCCGCCCGCGAGAACGCCGCC GTACGAGTACGCATGCGGGGACGAGGACCTGGGGCCGCTGTGACGCCGCCCGCGAGAACGCCGCC T C PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:334326..334429 26863196 MeRIP-seq:(Medium) rs769702405 Functional Loss SNV dbSNP153 33..33 33 - - - 82240 RMVar_ID_82240 Human_SNP_ID_707358668 m1A Human chrX - 334377 334377 334377 GTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACGCCGCCCGCGAGAACGCCGCC GTACGAGTACGCATGCGGGGACGAGGACCTGGCGCCGCTGTGACGCCGCCCGCGAGAACGCCGCC T G PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:334326..334429 26863196 MeRIP-seq:(Medium) rs769702405 Functional Loss SNV dbSNP153 33..33 33 - - - 82241 RMVar_ID_82241 Human_SNP_ID_707358677 m1A Human chrX - 334397 334386 334398 CCGCTGGGCGCCGTGGACCTGTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACG CCGCTGGGCGCCGTGGACCTGTACGAGTACG____________AGGACCTGGAGCCGCTGTGACG TCGTCCCCGCATG T PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1236851224 Functional Loss DEL dbSNP153 32..43 33 - - - 82242 RMVar_ID_82242 Human_SNP_ID_707358696 m1A Human chrX - 334397 334397 334397 CCGCTGGGCGCCGTGGACCTGTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACG CCGCTGGGCGCCGTGGACCTGTACGAGTACGCGTGCGGGGACGAGGACCTGGAGCCGCTGTGACG T C PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1133530 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 82243 RMVar_ID_82243 Human_SNP_ID_707358697 m1A Human chrX - 334397 334397 334397 CCGCTGGGCGCCGTGGACCTGTACGAGTACGCATGCGGGGACGAGGACCTGGAGCCGCTGTGACG CCGCTGGGCGCCGTGGACCTGTACGAGTACGCCTGCGGGGACGAGGACCTGGAGCCGCTGTGACG T G PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1133530 Functional Loss SNV dbSNP153 33..33 33 - - - 82244 RMVar_ID_82244 Human_SNP_ID_707360639 m1A Human chrX + 338581 338581 338581 ACTCACCCGTCCTCCCACTGACCCGTCCCCCCACTCACCCGTCCTCCCCACTCACCCGTCCTCCC ACTCACCCGTCCTCCCACTGACCCGTCCCCCCCCTCACCCGTCCTCCCCACTCACCCGTCCTCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:338348..338769 26863196 MeRIP-seq:(Medium) rs1270993216 Functional Loss SNV dbSNP153 33..33 33 - - - 82245 RMVar_ID_82245 Human_SNP_ID_707361729 m1A Human chrX - 340296 340296 340296 CCCGAGGGGTGACCTAGAGAACCTAGGGCCGGAGCTCACCGGGGACGTTGGCACTGGGCTGAGGG CCCGAGGGGTGACCTAGAGAACCTAGGGCCGGGGCTCACCGGGGACGTTGGCACTGGGCTGAGGG T C PPP2R3B Ensembl:ENSG00000167393 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:340294..340441 26863196 MeRIP-seq:(Medium) rs1463411135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1230462,Human_RBP_ID_3930512,Human_RBP_ID_18963360 RMVar_hsa_circ_261163,RMVar_hsa_circ_102987,RMVar_hsa_circ_292385,RMVar_hsa_circ_261165,RMVar_hsa_circ_77280,RMVar_hsa_circ_261164,RMVar_hsa_circ_88699,RMVar_hsa_circ_376560,RMVar_hsa_circ_261166 82246 RMVar_ID_82246 Human_SNP_ID_707362010 m1A Human chrX + 340701 340701 340701 CCTGGGCCGTCCTCTCGCCCGTCCGTCCCCTCACCCTGGGCCGTCCTCTCGCCCGTCCGTCCCCT CCTGGGCCGTCCTCTCGCCCGTCCGTCCCCTCTCCCTGGGCCGTCCTCTCGCCCGTCCGTCCCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:340631..340759 26863196 MeRIP-seq:(Medium) rs374933158 Functional Loss SNV dbSNP153 33..33 33 - - - 82247 RMVar_ID_82247 Human_SNP_ID_707370695 m1A Human chrX + 363221 363221 363221 GTCCTGGGGCAGGAGGTCCCTGCATCTCCCCGAGCCCGCGATCCCACAGTGCATCTCCCCGAGCC GTCCTGGGGCAGGAGGTCCCTGCATCTCCCCGTGCCCGCGATCCCACAGTGCATCTCCCCGAGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:363216..363711 26863196 MeRIP-seq:(Medium) rs1381970266 Functional Loss SNV dbSNP153 33..33 33 - - - 82248 RMVar_ID_82248 Human_SNP_ID_707370753 m1A Human chrX - 363296 363296 363296 TGCACTGTGGGATGGTGGGCTCGGGGAGATGCACTGCGGGATCGTGGGCTCGGGGAGATGCACTG TGCACTGTGGGATGGTGGGCTCGGGGAGATGCGCTGCGGGATCGTGGGCTCGGGGAGATGCACTG T C PPP2R3B Ensembl:ENSG00000167393 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:363282..363511 26863196 MeRIP-seq:(Medium) rs749597692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268960,Human_RBP_ID_3930524,Human_RBP_ID_5330643,Human_RBP_ID_8164688,Human_RBP_ID_8226431,Human_RBP_ID_8239714,Human_RBP_ID_8944842,Human_RBP_ID_9443407,Human_RBP_ID_18963363,Human_RBP_ID_21997216,Human_RBP_ID_22419657,Human_RBP_ID_22734188,Human_RBP_ID_26797215 82249 RMVar_ID_82249 Human_SNP_ID_707370764 m1A Human chrX + 363321 363321 363321 CCCGCAGTGCATCTCCCCGAGCCCACCATCCCACAGTGCATCTCCCCGAGCCCACCATCCCGCAG CCCGCAGTGCATCTCCCCGAGCCCACCATCCCGCAGTGCATCTCCCCGAGCCCACCATCCCGCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:363177..363738 26863196 MeRIP-seq:(Medium) rs748575648 Functional Loss SNV dbSNP153 33..33 33 - - - 82250 RMVar_ID_82250 Human_SNP_ID_707370833 m1A Human chrX + 363440 363440 363440 ACAGTGCATCTCCCCGAGCCCGCGATCCCACAATGCATCTCCCCGAGCCCACCATCCCACAATGC ACAGTGCATCTCCCCGAGCCCGCGATCCCACAGTGCATCTCCCCGAGCCCACCATCCCACAATGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:363198..363711;chrX:363222..363681 26863196 MeRIP-seq:(Medium) rs867428626 Functional Loss SNV dbSNP153 33..33 33 - - - 82251 RMVar_ID_82251 Human_SNP_ID_707379239 m1A Human chrX - 386342 386339 386342 GAGAGTAGTAAGTTACTCTTCCTTCTGCTAACAACTGCGCAGGTGGCTCTGGTCGCATAGTGGGC GAGAGTAGTAAGTTACTCTTCCTTCTGCTAAC___TGCGCAGGTGGCTCTGGTCGCATAGTGGGC AGTT A PPP2R3B Ensembl:ENSG00000167393 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:386339..386453 26863196 MeRIP-seq:(Medium) rs1376648106 Functional Loss DEL dbSNP153 33..35 33 - - - 82252 RMVar_ID_82252 Human_SNP_ID_707379268 m1A Human chrX - 386405 386405 386405 GGGCGCCGCCTCCAGCCCCAGGAACGCGCCCCACGTTCGAGGCACCCGTAGATCCGCAGGGACGA GGGCGCCGCCTCCAGCCCCAGGAACGCGCCCCTCGTTCGAGGCACCCGTAGATCCGCAGGGACGA T A PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:386402..386583 26863196 MeRIP-seq:(Medium) rs766321546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182471 82253 RMVar_ID_82253 Human_SNP_ID_707379269 m1A Human chrX - 386405 386405 386405 GGGCGCCGCCTCCAGCCCCAGGAACGCGCCCCACGTTCGAGGCACCCGTAGATCCGCAGGGACGA GGGCGCCGCCTCCAGCCCCAGGAACGCGCCCCGCGTTCGAGGCACCCGTAGATCCGCAGGGACGA T C PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:386402..386583 26863196 MeRIP-seq:(Medium) rs766321546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182471 82254 RMVar_ID_82254 Human_SNP_ID_707379476 m1A Human chrX + 386765 386741 386765 CGCCCCGCCCCGGGGGCTTCGGTCCGCCCCGGACCGACCTCGGTGATGCGAGCACGGCCCGCTGA CGCCCCGCC________________________CCGACCTCGGTGATGCGAGCACGGCCCGCTGA CCCGGGGGCTTCGGTCCGCCCCGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:386716..386886 26863196 MeRIP-seq:(Medium) rs1182537877 Functional Loss DEL dbSNP153 10..33 33 - - - 82255 RMVar_ID_82255 Human_SNP_ID_707379705 m1A Human chrX + 387272 387272 387272 AGCATGCGCCGTGCATAGCGGTGGAGGAGCGGAGTTCGGGAGGCCGGTCGGGTGAGCGTGCGCAA AGCATGCGCCGTGCATAGCGGTGGAGGAGCGGCGTTCGGGAGGCCGGTCGGGTGAGCGTGCGCAA A C AL732314.8 Ensembl:ENSG00000281849 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:387076..405434 26863196 MeRIP-seq:(Medium) rs1469800165 Functional Loss SNV dbSNP153 33..33 33 - - - 82256 RMVar_ID_82256 Human_SNP_ID_707384878 m1A Human chrX - 402887 402883 402887 ACTCACGCACTCACACATACCCTCACACACACATACTCAGTCACACATCAAAGCATTTTCATAGA ACTCACGCACTCACACATACCCTCACACACAC____TCAGTCACACATCAAAGCATTTTCATAGA AGTAT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:402871..403041 26863196 MeRIP-seq:(Medium) rs1169380609 Functional Loss DEL dbSNP153 33..36 33 - - - 82257 RMVar_ID_82257 Human_SNP_ID_707384880 m1A Human chrX - 402887 402886 402888 ACTCACGCACTCACACATACCCTCACACACACATACTCAGTCACACATCAAAGCATTTTCATAGA ACTCACGCACTCACACATACCCTCACACACA__TACTCAGTCACACATCAAAGCATTTTCATAGA ATG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:402871..403041 26863196 MeRIP-seq:(Medium) rs1035564567 Functional Loss DEL dbSNP153 32..33 33 - - - 82258 RMVar_ID_82258 Human_SNP_ID_707384928 m1A Human chrX - 402967 402952 402968 TCACAGAGCCAAATGCTGAATCACACACACATACCCTCACACACACACCCTCACACACACACACA TCACAGAGCCAAATGCTGAATCACACACACA________________CCCTCACACACACACACA GTGTGTGTGTGAGGGTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:402927..403133 26863196 MeRIP-seq:(Medium) rs1483493863 Functional Loss DEL dbSNP153 32..47 33 - - - 82259 RMVar_ID_82259 Human_SNP_ID_707384934 m1A Human chrX - 402967 402966 402968 TCACAGAGCCAAATGCTGAATCACACACACATACCCTCACACACACACCCTCACACACACACACA TCACAGAGCCAAATGCTGAATCACACACACA__CCCTCACACACACACCCTCACACACACACACA GTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:402927..403133 26863196 MeRIP-seq:(Medium) rs1200858542 Functional Loss DEL dbSNP153 32..33 33 - - - 82260 RMVar_ID_82260 Human_SNP_ID_707394840 m1A Human chrX + 427264 427246 427265 GACGGACGCCCCAGAGACAGCACGGAGACCCCAGAGACAGCACGGACACCCCCAGAGACAGGACG GACGGACGCCCCAGA___________________AGACAGCACGGACACCCCCAGAGACAGGACG AGACAGCACGGAGACCCCAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:427241..427405 26863196 MeRIP-seq:(Medium) rs1173562101 Functional Loss DEL dbSNP153 16..34 33 - - - 82261 RMVar_ID_82261 Human_SNP_ID_707712330 m1A Human chrX + 1250548 1250548 1250548 AGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGAGTAGATAGAAAGATAGAT AGATAGATAGATAGATAGATAGATAGATAGATGGATAGATAGATGGAGTAGATAGAAAGATAGAT A G RF00017-4520,RF00017-4495 RNACentral:URS000099C2D3,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1250547..1250666 26863196 MeRIP-seq:(Medium) rs756490075 Functional Loss SNV dbSNP153 33..33 33 - - - 82262 RMVar_ID_82262 Human_SNP_ID_707713450 m1A Human chrX + 1254116 1254113 1254117 TTGTTTCTGGAAAGGCAGGGAAGTATAAATAAACAAATGCTCAATGTCATCTGAAGGTGACATAC TTGTTTCTGGAAAGGCAGGGAAGTATAAAT____AAATGCTCAATGTCATCTGAAGGTGACATAC TAAAC T RF00017-4520,RF00017-4495 RNACentral:URS000099C2D3,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1254113..1254240 26863196 MeRIP-seq:(Medium) rs1359616938 Functional Loss DEL dbSNP153 31..34 33 - - - 82263 RMVar_ID_82263 Human_SNP_ID_707720413 m1A Human chrX + 1274777 1274777 1274777 CCTTTCACAGTTTACAGCAGGAAAATCCGTGGAGACAGCAGATCCGAGAAGCGGCGATGTTTGCG CCTTTCACAGTTTACAGCAGGAAAATCCGTGGGGACAGCAGATCCGAGAAGCGGCGATGTTTGCG A G CSF2RA Ensembl:ENSG00000198223 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1274772..1274837 26863196 MeRIP-seq:(Medium) rs1490851335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182516,Human_Splice_Rec_2182527,Human_Splice_Rec_2182543,Human_Splice_Rec_2182588,Human_Splice_Rec_2182592,Human_Splice_Rec_2182593,Human_Splice_Rec_2182596,Human_Splice_Rec_2182600,Human_Splice_Rec_2182608 RMVar_hsa_circ_9923 82264 RMVar_ID_82264 Human_SNP_ID_707724639 m1A Human chrX + 1285888 1285888 1285888 AAGAAAACACAACCTTCAGCAAGTGTTTCTTAACTGACAAGAAGAACAGAGTCGTGGAACCCAGG AAGAAAACACAACCTTCAGCAAGTGTTTCTTAGCTGACAAGAAGAACAGAGTCGTGGAACCCAGG A G CSF2RA Ensembl:ENSG00000198223 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1285843..1285983 26863196 MeRIP-seq:(Medium) rs1344102166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182518,Human_Splice_Rec_2182529,Human_Splice_Rec_2182545,Human_Splice_Rec_2182590 Human_miRNA_ID_643729,Human_miRNA_ID_2245941 RMVar_hsa_circ_9923,RMVar_hsa_circ_59214,RMVar_hsa_circ_74607,RMVar_hsa_circ_310334,RMVar_hsa_circ_38727,RMVar_hsa_circ_261174,RMVar_hsa_circ_305833 82265 RMVar_ID_82265 Human_SNP_ID_707728935 m1A Human chrX + 1295843 1295843 1295843 CCCTGCCCCACGTCCACCTAGCTTAATCCTACAGTCCCCTACTCACCACACCTAATGTAACTCTA CCCTGCCCCACGTCCACCTAGCTTAATCCTACGGTCCCCTACTCACCACACCTAATGTAACTCTA A G CSF2RA Ensembl:ENSG00000198223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1295799..1295905 26863196 MeRIP-seq:(Medium) rs1447391534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9923,RMVar_hsa_circ_74607 82266 RMVar_ID_82266 Human_SNP_ID_707729019 m1A Human chrX + 1296000 1295999 1296001 AGTCCCCTACTCACGACCCCCGGAGTAATCCTACAGTCTCCTACTCACGACGCCTACAGTTCCCT AGTCCCCTACTCACGACCCCCGGAGTAATCCT__AGTCTCCTACTCACGACGCCTACAGTTCCCT TAC T CSF2RA Ensembl:ENSG00000198223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1295970..1296068 26863196 MeRIP-seq:(Medium) rs1465579907 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_9923,RMVar_hsa_circ_74607 82267 RMVar_ID_82267 Human_SNP_ID_707729160 m1A Human chrX + 1296260 1296249 1296260 CCTACACTCCCCTACTCACAACCCCTAGTGTAACCCTACAGTCTCCTACCCATGACCCCTGGCGG CCTACACTCCCCTACTCACAAC___________CCCTACAGTCTCCTACCCATGACCCCTGGCGG CCCCTAGTGTAA C CSF2RA Ensembl:ENSG00000198223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1296185..1296305 26863196 MeRIP-seq:(Medium) rs1411903686 Functional Loss DEL dbSNP153 23..33 33 - - - RMVar_hsa_circ_9923,RMVar_hsa_circ_74607 82268 RMVar_ID_82268 Human_SNP_ID_707732899 m1A Human chrX + 1306223 1306219 1306223 TGAGGAGACACAAAAGAGAGGGAAACAGGCAGACAGACTGACAGAAACAAAGGCAGACACACAGA TGAGGAGACACAAAAGAGAGGGAAACAGG____CAGACTGACAGAAACAAAGGCAGACACACAGA GCAGA G CSF2RA Ensembl:ENSG00000198223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1306085..1306410 26863196 MeRIP-seq:(Medium) rs756897659 Functional Loss DEL dbSNP153 30..33 33 - - - 82269 RMVar_ID_82269 Human_SNP_ID_707733073 m1A Human chrX + 1306835 1306832 1306836 ACAAAGAGAAAAAGACGGACAGAGAGAGAAACAGAGAGACATAGGTGGACACAGAGAGGGGAGAG ACAAAGAGAAAAAGACGGACAGAGAGAGAA____AGAGACATAGGTGGACACAGAGAGGGGAGAG AACAG A CSF2RA Ensembl:ENSG00000198223 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1306731..1306967 26863196 MeRIP-seq:(Medium) rs1395742502 Functional Loss DEL dbSNP153 31..34 33 - - - 82270 RMVar_ID_82270 Human_SNP_ID_707751339 m1A Human chrX - 1348629 1348626 1348630 AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAAAAAAGACACAGCGAAGGCGAGAGGGAGGGAGAGA AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAA____GACACAGCGAAGGCGAGAGGGAGGGAGAGA CTTTT C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1348625..1348811 26863196 MeRIP-seq:(Medium) rs1163307070 Functional Loss DEL dbSNP153 32..35 33 - - - 82271 RMVar_ID_82271 Human_SNP_ID_707751340 m1A Human chrX - 1348629 1348626 1348630 AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAAAAAAGACACAGCGAAGGCGAGAGGGAGGGAGAGA AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAA___AGACACAGCGAAGGCGAGAGGGAGGGAGAGA CTTTT CT RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1348625..1348811 26863196 MeRIP-seq:(Medium) rs1163307070 Functional Loss DEL dbSNP153 32..34 33 - - - 82272 RMVar_ID_82272 Human_SNP_ID_707751341 m1A Human chrX - 1348629 1348626 1348630 AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAAAAAAGACACAGCGAAGGCGAGAGGGAGGGAGAGA AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAA__AAGACACAGCGAAGGCGAGAGGGAGGGAGAGA CTTTT CTT RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1348625..1348811 26863196 MeRIP-seq:(Medium) rs1163307070 Functional Loss DEL dbSNP153 32..33 33 - - - 82273 RMVar_ID_82273 Human_SNP_ID_707751345 m1A Human chrX - 1348629 1348629 1348629 AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAAAAAAGACACAGCGAAGGCGAGAGGGAGGGAGAGA AAAGAAAGAAAGAAAGAGAAAAAGAAAAGAAAGAAGACACAGCGAAGGCGAGAGGGAGGGAGAGA T C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1348625..1348811 26863196 MeRIP-seq:(Medium) rs1351041783 Functional Loss SNV dbSNP153 33..33 33 - - - 82274 RMVar_ID_82274 Human_SNP_ID_707756342 m1A Human chrX + 1359989 1359989 1359989 CTGTCTCTGTATCTCTCTCCCTTTCTCCCTCCATCTTTCTCTCTCTCCCCCGGTCTCTATCTTCC CTGTCTCTGTATCTCTCTCCCTTTCTCCCTCCCTCTTTCTCTCTCTCCCCCGGTCTCTATCTTCC A C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1359984..1360164 26863196 MeRIP-seq:(Medium) rs1401830801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2137863,Human_miRNA_ID_2610470,Human_miRNA_ID_2666643 RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82275 RMVar_ID_82275 Human_SNP_ID_707756421 m1A Human chrX - 1360114 1360112 1360114 ACAGAGACAGACACGGAGAAAGAGACGGGGAGAGGGGGAGATAGAGACCGGGAGAGAGAGAGAAA ACAGAGACAGACACGGAGAAAGAGACGGGGAG__GGGGAGATAGAGACCGGGAGAGAGAGAGAAA CCT C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:1359941..1360129 26863196 MeRIP-seq:(Medium) rs1213275671 Functional Loss DEL dbSNP153 33..34 33 - - - 82276 RMVar_ID_82276 Human_SNP_ID_707756422 m1A Human chrX - 1360114 1360113 1360114 ACAGAGACAGACACGGAGAAAGAGACGGGGAGAGGGGGAGATAGAGACCGGGAGAGAGAGAGAAA ACAGAGACAGACACGGAGAAAGAGACGGGGAG_GGGGGAGATAGAGACCGGGAGAGAGAGAGAAA CT C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:1359941..1360129 26863196 MeRIP-seq:(Medium) rs1284411201 Functional Loss DEL dbSNP153 33..33 33 - - - 82277 RMVar_ID_82277 Human_SNP_ID_707756790 m1A Human chrX - 1360844 1360844 1360844 AGGGGAAGGGAGAGAGAGACAGGGAGAGAGCTAGAAAGATAAAGAGAGGGGCCGGGCACGGTGGC AGGGGAAGGGAGAGAGAGACAGGGAGAGAGCTCGAAAGATAAAGAGAGGGGCCGGGCACGGTGGC T G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1360793..1360907 26863196 MeRIP-seq:(Medium) rs1214427956 Functional Loss SNV dbSNP153 33..33 33 - - - 82278 RMVar_ID_82278 Human_SNP_ID_707756976 m1A Human chrX - 1361178 1361176 1361179 AGAGACAGGGGAATGGAGAGAGAGAGAGGGGAAGGGAGAGAGAGACAGAGAAGGAAAGGGAGAGA AGAGACAGGGGAATGGAGAGAGAGAGAGGGG___GGAGAGAGAGACAGAGAAGGAAAGGGAGAGA CCTT C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1361099..1361320 26863196 MeRIP-seq:(Medium) rs1327739321 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17070702 82279 RMVar_ID_82279 Human_SNP_ID_707756995 m1A Human chrX - 1361192 1361192 1361192 AAAGGGAGAGACATAGAGACAGGGGAATGGAGAGAGAGAGAGGGGAAGGGAGAGAGAGACAGAGA AAAGGGAGAGACATAGAGACAGGGGAATGGAGTGAGAGAGAGGGGAAGGGAGAGAGAGACAGAGA T A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1361188..1361267 26863196 MeRIP-seq:(Medium) rs1351890114 Functional Loss SNV dbSNP153 33..33 33 - - - 82280 RMVar_ID_82280 Human_SNP_ID_707757508 m1A Human chrX - 1362157 1362156 1362158 AAAGACATAGATACAAAGAGAGAGGGAAAGAGAAAAACAGAAAAACAGAAACAGAGAGACATAGA AAAGACATAGATACAAAGAGAGAGGGAAAGA__AAAACAGAAAAACAGAAACAGAGAGACATAGA TTC T RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:1362081..1362393 26863196 MeRIP-seq:(Medium) rs1419643089 Functional Loss DEL dbSNP153 32..33 33 - - - 82281 RMVar_ID_82281 Human_SNP_ID_707757524 m1A Human chrX - 1362175 1362172 1362176 ACAGAAACGGAGAGACAGAAAGACATAGATACAAAGAGAGAGGGAAAGAGAAAAACAGAAAAACA ACAGAAACGGAGAGACAGAAAGACATAGATA____GAGAGAGGGAAAGAGAAAAACAGAAAAACA CTTTG C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chrX:1361974..1362262;chrX:1361974..1362615 26863196 MeRIP-seq:(Medium) rs1304907839 Functional Loss DEL dbSNP153 32..35 33 - - - 82282 RMVar_ID_82282 Human_SNP_ID_707757531 m1A Human chrX - 1362187 1362184 1362188 ACAGAGAGAGAGACAGAAACGGAGAGACAGAAAGACATAGATACAAAGAGAGAGGGAAAGAGAAA ACAGAGAGAGAGACAGAAACGGAGAGACAGA____CATAGATACAAAGAGAGAGGGAAAGAGAAA GTCTT G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1362182..1362311 26863196 MeRIP-seq:(Medium) rs1431894588 Functional Loss DEL dbSNP153 32..35 33 - - - 82283 RMVar_ID_82283 Human_SNP_ID_707757535 m1A Human chrX - 1362187 1362187 1362187 ACAGAGAGAGAGACAGAAACGGAGAGACAGAAAGACATAGATACAAAGAGAGAGGGAAAGAGAAA ACAGAGAGAGAGACAGAAACGGAGAGACAGAATGACATAGATACAAAGAGAGAGGGAAAGAGAAA T A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1362182..1362311 26863196 MeRIP-seq:(Medium) rs1194619753 Functional Loss SNV dbSNP153 33..33 33 - - - 82284 RMVar_ID_82284 Human_SNP_ID_707757689 m1A Human chrX - 1362453 1362450 1362454 ATGGACAGAGAGAGACAGATAGAAACAGAGAGAGACAGAGATACAAAGAGACACAGAGAAGGGAG ATGGACAGAGAGAGACAGATAGAAACAGAGA____CAGAGATACAAAGAGACACAGAGAAGGGAG GTCTC G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1362338..1362500 26863196 MeRIP-seq:(Medium) rs774782223 Functional Loss DEL dbSNP153 32..35 33 - - - 82285 RMVar_ID_82285 Human_SNP_ID_707757690 m1A Human chrX - 1362453 1362450 1362454 ATGGACAGAGAGAGACAGATAGAAACAGAGAGAGACAGAGATACAAAGAGACACAGAGAAGGGAG ATGGACAGAGAGAGACAGATAGAAACAGAGA__GACAGAGATACAAAGAGACACAGAGAAGGGAG GTCTC GTC RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1362338..1362500 26863196 MeRIP-seq:(Medium) rs774782223 Functional Loss DEL dbSNP153 32..33 33 - - - 82286 RMVar_ID_82286 Human_SNP_ID_707758921 m1A Human chrX + 1365355 1365337 1365355 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGC__________________GCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG CGCGGGGTGAGCGGGGTGA C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1448303602 Functional Loss DEL dbSNP153 16..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82287 RMVar_ID_82287 Human_SNP_ID_707758922 m1A Human chrX + 1365355 1365337 1365355 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGCGCGGGGTGA_________GCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG CGCGGGGTGAGCGGGGTGA CGCGGGGTGA IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1448303602 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82288 RMVar_ID_82288 Human_SNP_ID_707758936 m1A Human chrX + 1365355 1365348 1365355 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGCGCGGGGTGAGC_______GCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG CGGGGTGA C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1569526200 Functional Loss DEL dbSNP153 27..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82289 RMVar_ID_82289 Human_SNP_ID_707758937 m1A Human chrX + 1365355 1365348 1365356 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGCGCGGGGTGAGC________CGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG CGGGGTGAG C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1569526201 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82290 RMVar_ID_82290 Human_SNP_ID_707758943 m1A Human chrX + 1365355 1365355 1365355 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGCGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG A C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1302197978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82291 RMVar_ID_82291 Human_SNP_ID_707758944 m1A Human chrX + 1365355 1365355 1365355 GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG GGGTGAGCGGGGTGCGCGGGGTGAGCGGGGTGGGCGGGGTGAGCCGGGTGCGCGGGGTGAGCCGG A G IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1365277..1365395 26863196 MeRIP-seq:(Medium) rs1302197978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82292 RMVar_ID_82292 Human_SNP_ID_707759076 m1A Human chrX + 1365580 1365580 1365580 GGGTGAGCCGGGTGCGCGGGGTGAGCGGGGTGAGCCGGGTGCGCGGGGTGAGCGGGGTGAGCGGG GGGTGAGCCGGGTGCGCGGGGTGAGCGGGGTGCGCCGGGTGCGCGGGGTGAGCGGGGTGAGCGGG A C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:1365479..1365604 26863410 MeRIP-seq:(Medium) rs767032613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79783,RMVar_hsa_circ_261177 82293 RMVar_ID_82293 Human_SNP_ID_707765590 m1A Human chrX - 1386449 1386449 1386449 TCCTGCCTGTAGATGGCCGGGGAAGGCTCTAGAAAAGGGGCGCATTGCGATCCAACCATCGGCAG TCCTGCCTGTAGATGGCCGGGGAAGGCTCTAGGAAAGGGGCGCATTGCGATCCAACCATCGGCAG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1386401..1386650 26863196 MeRIP-seq:(Medium) rs1279062948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186914,Human_RBP_ID_1341445,Human_RBP_ID_2071799,Human_RBP_ID_3918616,Human_RBP_ID_5230724,Human_RBP_ID_8714813,Human_RBP_ID_17327654,Human_RBP_ID_17442657,Human_RBP_ID_17556097,Human_RBP_ID_17717851,Human_RBP_ID_18147400,Human_RBP_ID_18916857,Human_RBP_ID_22122662 Human_miRNA_ID_2798120,Human_miRNA_ID_2798121,Human_miRNA_ID_2798122,Human_miRNA_ID_2798123,Human_miRNA_ID_2799084,Human_miRNA_ID_2799085,Human_miRNA_ID_2799086,Human_miRNA_ID_2799087,Human_miRNA_ID_2800467,Human_miRNA_ID_2800468,Human_miRNA_ID_2800469,Human_miRNA_ID_2800470,Human_miRNA_ID_2807780,Human_miRNA_ID_2807781,Human_miRNA_ID_2807782,Human_miRNA_ID_2807783,Human_miRNA_ID_2810924,Human_miRNA_ID_2810925,Human_miRNA_ID_2810926,Human_miRNA_ID_2810927,Human_miRNA_ID_2814066,Human_miRNA_ID_2814067,Human_miRNA_ID_2814068,Human_miRNA_ID_2814069,Human_miRNA_ID_2833658,Human_miRNA_ID_2833659,Human_miRNA_ID_2833660,Human_miRNA_ID_2833661,Human_miRNA_ID_2853179,Human_miRNA_ID_2853180,Human_miRNA_ID_2853181,Human_miRNA_ID_2853182,Human_miRNA_ID_2854241,Human_miRNA_ID_2854242,Human_miRNA_ID_2854243,Human_miRNA_ID_2854244,Human_miRNA_ID_2861325,Human_miRNA_ID_2861326,Human_miRNA_ID_2861327,Human_miRNA_ID_2861328 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_127294,RMVar_hsa_circ_89907,RMVar_hsa_circ_261180,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 82294 RMVar_ID_82294 Human_SNP_ID_707765598 m1A Human chrX - 1386469 1386469 1386469 TTGTCTTTTTCCCAGCCGCATCCTGCCTGTAGATGGCCGGGGAAGGCTCTAGAAAAGGGGCGCAT TTGTCTTTTTCCCAGCCGCATCCTGCCTGTAGGTGGCCGGGGAAGGCTCTAGAAAAGGGGCGCAT T C SLC25A6 Ensembl:ENSG00000169100 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:1386419..1386604 26863196 MeRIP-seq:(Medium) rs1272933638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712160,Human_RBP_ID_2071799,Human_RBP_ID_3246614,Human_RBP_ID_3918616,Human_RBP_ID_7985825,Human_RBP_ID_8714813,Human_RBP_ID_17325367,Human_RBP_ID_17442657,Human_RBP_ID_17553369,Human_RBP_ID_18147400,Human_RBP_ID_18197246,Human_RBP_ID_18916857,Human_RBP_ID_22122662,Human_RBP_ID_23216796,Human_RBP_ID_27550215 Human_miRNA_ID_2798120,Human_miRNA_ID_2798121,Human_miRNA_ID_2798122,Human_miRNA_ID_2798123,Human_miRNA_ID_2799084,Human_miRNA_ID_2799085,Human_miRNA_ID_2799086,Human_miRNA_ID_2799087,Human_miRNA_ID_2800467,Human_miRNA_ID_2800468,Human_miRNA_ID_2800469,Human_miRNA_ID_2800470,Human_miRNA_ID_2807780,Human_miRNA_ID_2807781,Human_miRNA_ID_2807782,Human_miRNA_ID_2807783,Human_miRNA_ID_2810924,Human_miRNA_ID_2810925,Human_miRNA_ID_2810926,Human_miRNA_ID_2810927,Human_miRNA_ID_2814066,Human_miRNA_ID_2814067,Human_miRNA_ID_2814068,Human_miRNA_ID_2814069,Human_miRNA_ID_2833658,Human_miRNA_ID_2833659,Human_miRNA_ID_2833660,Human_miRNA_ID_2833661,Human_miRNA_ID_2853179,Human_miRNA_ID_2853180,Human_miRNA_ID_2853181,Human_miRNA_ID_2853182,Human_miRNA_ID_2854241,Human_miRNA_ID_2854242,Human_miRNA_ID_2854243,Human_miRNA_ID_2854244,Human_miRNA_ID_2861325,Human_miRNA_ID_2861326,Human_miRNA_ID_2861327,Human_miRNA_ID_2861328 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_127294,RMVar_hsa_circ_89907,RMVar_hsa_circ_261180,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 82295 RMVar_ID_82295 Human_SNP_ID_707765612 m1A Human chrX - 1386523 1386523 1386523 AGAACCACGTAGAATCCTCAACCGTGCGGACCATCAACCTTCGAGAAATTCCAGTTGTCTTTTTC AGAACCACGTAGAATCCTCAACCGTGCGGACCGTCAACCTTCGAGAAATTCCAGTTGTCTTTTTC T C SLC25A6 Ensembl:ENSG00000169100 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:1386401..1386674 26863196 MeRIP-seq:(Medium) rs1379775776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1229853,Human_RBP_ID_1712160,Human_RBP_ID_2071799,Human_RBP_ID_3918616,Human_RBP_ID_5233397,Human_RBP_ID_8714815,Human_RBP_ID_17325369,Human_RBP_ID_17442659,Human_RBP_ID_17553370,Human_RBP_ID_18916860,Human_RBP_ID_23216796,Human_RBP_ID_27550217 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_127294,RMVar_hsa_circ_89907,RMVar_hsa_circ_261180,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 82296 RMVar_ID_82296 Human_SNP_ID_707765657 m1A Human chrX + 1386590 1386590 1386590 TGGTTCCCCTGGTGTGTGTGTGTGTGTGGAGGAGGCCGCGGCCCTTAGATCACCTTCTTGAGCTC TGGTTCCCCTGGTGTGTGTGTGTGTGTGGAGGCGGCCGCGGCCCTTAGATCACCTTCTTGAGCTC A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:1386488..1386675 26863410 MeRIP-seq:(Medium) rs753794844 Functional Loss SNV dbSNP153 33..33 33 - - - 82297 RMVar_ID_82297 Human_SNP_ID_707765664 m1A Human chrX - 1386602 1386602 1386602 GTCCTGTACGACGAGCTCAAGAAGGTGATCTAAGGGCCGCGGCCTCCTCCACACACACACACACA GTCCTGTACGACGAGCTCAAGAAGGTGATCTAGGGGCCGCGGCCTCCTCCACACACACACACACA T C SLC25A6 Ensembl:ENSG00000169100 Protein coding stop codon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:1386505..1386620 26863196 MeRIP-seq:(Medium) rs1264470127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712163,Human_RBP_ID_2071802,Human_RBP_ID_3918619,Human_RBP_ID_7985828,Human_RBP_ID_8714816,Human_RBP_ID_17325371,Human_RBP_ID_17440626,Human_RBP_ID_17553371,Human_RBP_ID_18197534,Human_RBP_ID_18916864,Human_RBP_ID_26834539,Human_RBP_ID_27550218 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_127294,RMVar_hsa_circ_89907,RMVar_hsa_circ_261180,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 82298 RMVar_ID_82298 Human_SNP_ID_707766005 m1A Human chrX - 1387375 1387375 1387375 ACCCCAAGAACACGCACATCGTGGTGAGCTGGATGATCGCGCAGACCGTGACGGCCGTGGCCGGC ACCCCAAGAACACGCACATCGTGGTGAGCTGGGTGATCGCGCAGACCGTGACGGCCGTGGCCGGC T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1387351..1387375 26863196 MeRIP-seq:(Medium) rs1394374004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712212,Human_RBP_ID_2071862,Human_RBP_ID_8933572,Human_RBP_ID_18147493,Human_RBP_ID_18197250,Human_RBP_ID_18916905 Human_Splice_Rec_2182670,Human_Splice_Rec_2182674 Human_miRNA_ID_2899477,Human_miRNA_ID_2899478,Human_miRNA_ID_2899479 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_89907,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 82299 RMVar_ID_82299 Human_SNP_ID_707766712 m1A Human chrX - 1389212 1389212 1389212 AAGGGTACGTGTGGCTGCCATCGCGAAGTCCCAGAGACGGGCTCAACACACAGACGTTCCCCCAG AAGGGTACGTGTGGCTGCCATCGCGAAGTCCCGGAGACGGGCTCAACACACAGACGTTCCCCCAG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1389209..1389760 26863196 MeRIP-seq:(Medium) rs769077785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19148157 Human_miRNA_ID_2425966,Human_miRNA_ID_2425967,Human_miRNA_ID_2435637,Human_miRNA_ID_2435638 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183 82300 RMVar_ID_82300 Human_SNP_ID_707766726 m1A Human chrX + 1389233 1389233 1389233 GAGCCCGTCTCTGGGACTTCGCGATGGCAGCCACACGTACCCTTGGCCGTATCGTACACGCCGAA GAGCCCGTCTCTGGGACTTCGCGATGGCAGCCGCACGTACCCTTGGCCGTATCGTACACGCCGAA A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:1389226..1389250 26863196 MeRIP-seq:(Medium) rs1373224201 Functional Loss SNV dbSNP153 33..33 33 - - - 82301 RMVar_ID_82301 Human_SNP_ID_707767815 m1A Human chrX - 1391943 1391943 1391943 TCTTGGCCGGAGGCATCGCCGCCGCCATCTCCAAGACGGCCGTGGCTCCGATCGAGCGGGTCAAG TCTTGGCCGGAGGCATCGCCGCCGCCATCTCCGAGACGGCCGTGGCTCCGATCGAGCGGGTCAAG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:1391926..1392100 32194978 MeRIP-seq:(Medium) rs768118492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17442663,Human_RBP_ID_18197256,Human_RBP_ID_22123360,Human_RBP_ID_22534568,Human_RBP_ID_27550253 Human_Splice_Rec_2182669 Human_miRNA_ID_1985634,Human_miRNA_ID_2616508,Human_miRNA_ID_2941281 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 82302 RMVar_ID_82302 Human_SNP_ID_707767818 m1A Human chrX - 1391949 1391949 1391949 AAGACTTCTTGGCCGGAGGCATCGCCGCCGCCATCTCCAAGACGGCCGTGGCTCCGATCGAGCGG AAGACTTCTTGGCCGGAGGCATCGCCGCCGCCGTCTCCAAGACGGCCGTGGCTCCGATCGAGCGG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:1391835..1392075 26863196 MeRIP-seq:(Medium) rs1219753229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7986373,Human_RBP_ID_17325432,Human_RBP_ID_17442663,Human_RBP_ID_18197256,Human_RBP_ID_18916937,Human_RBP_ID_22123360,Human_RBP_ID_22534568,Human_RBP_ID_26834547,Human_RBP_ID_27550253 Human_Splice_Rec_2182669 Human_miRNA_ID_1985634,Human_miRNA_ID_2616508,Human_miRNA_ID_2941281 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 82303 RMVar_ID_82303 Human_SNP_ID_707767844 m1A Human chrX - 1391999 1391999 1391999 TTCCGCTGCCCGCCCTGCCACCATGACGGAACAGGCCATCTCCTTCGCCAAAGACTTCTTGGCCG TTCCGCTGCCCGCCCTGCCACCATGACGGAACGGGCCATCTCCTTCGCCAAAGACTTCTTGGCCG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1391841..1392125 26863196 MeRIP-seq:(Medium) rs1356184383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712235,Human_RBP_ID_2071872,Human_RBP_ID_3918719,Human_RBP_ID_7986374,Human_RBP_ID_8714918,Human_RBP_ID_18197257,Human_RBP_ID_18916938,Human_RBP_ID_22534568,Human_RBP_ID_26834548 Human_miRNA_ID_1979727,Human_miRNA_ID_2622186 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 82304 RMVar_ID_82304 Human_SNP_ID_707767845 m1A Human chrX - 1391999 1391999 1391999 TTCCGCTGCCCGCCCTGCCACCATGACGGAACAGGCCATCTCCTTCGCCAAAGACTTCTTGGCCG TTCCGCTGCCCGCCCTGCCACCATGACGGAACCGGCCATCTCCTTCGCCAAAGACTTCTTGGCCG T G SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1391841..1392125 26863196 MeRIP-seq:(Medium) rs1356184383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712235,Human_RBP_ID_2071872,Human_RBP_ID_3918719,Human_RBP_ID_7986374,Human_RBP_ID_8714918,Human_RBP_ID_18197257,Human_RBP_ID_18916938,Human_RBP_ID_22534568,Human_RBP_ID_26834548 Human_miRNA_ID_1979727,Human_miRNA_ID_2622186 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 82305 RMVar_ID_82305 Human_SNP_ID_707767896 m1A Human chrX - 1392081 1392081 1392081 CCTTTCGGTCCAGGCGGCGGCAGGGCTGAGCCAGCGACGCCCTCCATTCACTCTCCGCGCCCGTT CCTTTCGGTCCAGGCGGCGGCAGGGCTGAGCCTGCGACGCCCTCCATTCACTCTCCGCGCCCGTT T A SLC25A6 Ensembl:ENSG00000169100 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:1391997..1392085 26863410 MeRIP-seq:(Medium) rs1250585812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076450,Human_RBP_ID_22468650,Human_RBP_ID_22534569,Human_RBP_ID_27550255 Human_miRNA_ID_2084674,Human_miRNA_ID_2270826 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 82306 RMVar_ID_82306 Human_SNP_ID_707767997 m1A Human chrX - 1392229 1392229 1392229 GATTCCCGGCAGCCCTCAGAGGCGAGGCACGCAGGCTGGTGTGGGGCGGGGCCTGGCGGCGCAGC GATTCCCGGCAGCCCTCAGAGGCGAGGCACGCTGGCTGGTGTGGGGCGGGGCCTGGCGGCGCAGC T A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1392180..1392277 26863196 MeRIP-seq:(Medium) rs1312226500 Functional Loss SNV dbSNP153 33..33 33 - - - 82307 RMVar_ID_82307 Human_SNP_ID_707768000 m1A Human chrX - 1392237 1392237 1392237 CGCAGCGGGATTCCCGGCAGCCCTCAGAGGCGAGGCACGCAGGCTGGTGTGGGGCGGGGCCTGGC CGCAGCGGGATTCCCGGCAGCCCTCAGAGGCGCGGCACGCAGGCTGGTGTGGGGCGGGGCCTGGC T G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1392188..1392314 26863196 MeRIP-seq:(Medium) rs1168120912 Functional Loss SNV dbSNP153 33..33 33 - - - 82308 RMVar_ID_82308 Human_SNP_ID_707768128 m1A Human chrX - 1392494 1392494 1392494 GGCCTCCGGGAGAAAGCGGACGACGCACTCGGAGCGAACTGGGCATCAGGGTGGGCTTCTGACTC GGCCTCCGGGAGAAAGCGGACGACGCACTCGGGGCGAACTGGGCATCAGGGTGGGCTTCTGACTC T C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1392445..1392859 26863196 MeRIP-seq:(Medium) rs1458856988 Functional Loss SNV dbSNP153 33..33 33 - - - 82309 RMVar_ID_82309 Human_SNP_ID_707768687 m1A Human chrX + 1393226 1393226 1393226 TCCTTTCTTGCTACGTTTCTTCCCTCTTTTTCATTTTTTTCCTTCCTTTTTCTGCTTTTCTCCCT TCCTTTCTTGCTACGTTTCTTCCCTCTTTTTCCTTTTTTTCCTTCCTTTTTCTGCTTTTCTCCCT A C LINC00106,RF00017-4495,LINC00106:2,LINC00106:3,LINC00106:4 RNACentral:URS0000D5BB91,RNACentral:URS0000923EDC,RNACentral:URS0000D58D85,RNACentral:URS0000D5CE62,RNACentral:URS0000D5A19E lincRNA,SRP RNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1393176..1393323 26863196 MeRIP-seq:(Medium) rs1317083556 Functional Loss SNV dbSNP153 33..33 33 - - - 82310 RMVar_ID_82310 Human_SNP_ID_707768688 m1A Human chrX + 1393226 1393226 1393226 TCCTTTCTTGCTACGTTTCTTCCCTCTTTTTCATTTTTTTCCTTCCTTTTTCTGCTTTTCTCCCT TCCTTTCTTGCTACGTTTCTTCCCTCTTTTTCTTTTTTTTCCTTCCTTTTTCTGCTTTTCTCCCT A T LINC00106,RF00017-4495,LINC00106:2,LINC00106:3,LINC00106:4 RNACentral:URS0000D5BB91,RNACentral:URS0000923EDC,RNACentral:URS0000D58D85,RNACentral:URS0000D5CE62,RNACentral:URS0000D5A19E lincRNA,SRP RNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1393176..1393323 26863196 MeRIP-seq:(Medium) rs1317083556 Functional Loss SNV dbSNP153 33..33 33 - - - 82311 RMVar_ID_82311 Human_SNP_ID_707769226 m1A Human chrX - 1394316 1394316 1394316 AAAGAGCAAAGGAGACAGGGAGACAGGAAAGAAAAAGGGGAGGGAGGCAAACGGGGAACGGGAGA AAAGAGCAAAGGAGACAGGGAGACAGGAAAGACAAAGGGGAGGGAGGCAAACGGGGAACGGGAGA T G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1394296..1394559 26863196 MeRIP-seq:(Medium) rs765319233 Functional Loss SNV dbSNP153 33..33 33 - - - 82312 RMVar_ID_82312 Human_SNP_ID_707769536 m1A Human chrX + 1394914 1394914 1394914 GTCACTGAGGCATGGGTAGGTCTAACCTTGGGACATTGCTGTGGGGAGGGCTGTGGAGACCAAGC GTCACTGAGGCATGGGTAGGTCTAACCTTGGGGCATTGCTGTGGGGAGGGCTGTGGAGACCAAGC A G LINC00106,RF00017-4495,LINC00106:2,LINC00106:3,LINC00106:4,LINC00106:5 RNACentral:URS0000D5BB91,RNACentral:URS0000923EDC,RNACentral:URS00009AF202,RNACentral:URS0000D58D85,RNACentral:URS0000D5CE62,RNACentral:URS0000D5A19E lincRNA,SRP RNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1394864..1395043 26863196 MeRIP-seq:(Medium) rs1324202438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1229881 82313 RMVar_ID_82313 Human_SNP_ID_707769894 m1A Human chrX - 1395786 1395767 1395786 TCCATCCATCCATCCATCATCCATCCATCTATACATTATCCATCCATCTATCCATTATCCATCCA TCCATCCATCCATCCATCATCCATCCATCTAT___________________CCATTATCCATCCA GATAGATGGATGGATAATGT G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1395735..1395898 26863196 MeRIP-seq:(Medium) rs1426404713 Functional Loss DEL dbSNP153 33..51 33 - - - 82314 RMVar_ID_82314 Human_SNP_ID_707769901 m1A Human chrX - 1395786 1395786 1395786 TCCATCCATCCATCCATCATCCATCCATCTATACATTATCCATCCATCTATCCATTATCCATCCA TCCATCCATCCATCCATCATCCATCCATCTATTCATTATCCATCCATCTATCCATTATCCATCCA T A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1395735..1395898 26863196 MeRIP-seq:(Medium) rs868651537 Functional Loss SNV dbSNP153 33..33 33 - - - 82315 RMVar_ID_82315 Human_SNP_ID_707769902 m1A Human chrX - 1395786 1395786 1395786 TCCATCCATCCATCCATCATCCATCCATCTATACATTATCCATCCATCTATCCATTATCCATCCA TCCATCCATCCATCCATCATCCATCCATCTATCCATTATCCATCCATCTATCCATTATCCATCCA T G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1395735..1395898 26863196 MeRIP-seq:(Medium) rs868651537 Functional Loss SNV dbSNP153 33..33 33 - - - 82316 RMVar_ID_82316 Human_SNP_ID_707769906 m1A Human chrX - 1395792 1395789 1395793 CCATTATCCATCCATCCATCCATCATCCATCCATCTATACATTATCCATCCATCTATCCATTATC CCATTATCCATCCATCCATCCATCATCCATC____TATACATTATCCATCCATCTATCCATTATC AGATG A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1395741..1395916 26863196 MeRIP-seq:(Medium) rs1415260381 Functional Loss DEL dbSNP153 32..35 33 - - - 82317 RMVar_ID_82317 Human_SNP_ID_707770037 m1A Human chrX - 1396101 1396098 1396102 CAGAATCATTTACCAAGCAAACACATCCATCTATCCATCCATCCACCCACTCATTGATTATCCAT CAGAATCATTTACCAAGCAAACACATCCATC____CATCCATCCACCCACTCATTGATTATCCAT GGATA G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1396050..1396292 26863196 MeRIP-seq:(Medium) rs1340665781 Functional Loss DEL dbSNP153 32..35 33 - - - 82318 RMVar_ID_82318 Human_SNP_ID_707770459 m1A Human chrX - 1397471 1397471 1397471 GGGCCTTTTGAGGAGCCCTTTTCAGGGGGGTGACCCTGGGAGTCCCTTTTCAGGGATGAGGTCTT GGGCCTTTTGAGGAGCCCTTTTCAGGGGGGTGTCCCTGGGAGTCCCTTTTCAGGGATGAGGTCTT T A RF00017-6698,RF00017-4643,lnc-SLC25A6-1-001,lnc-SLC25A6-1-001:2 RNACentral:URS000099749B,RNACentral:URS00009A02E8,RNACentral:URS00008BABFF,RNACentral:URS00008B417D SRP RNA,SRP RNA,lincRNA,lincRNA intron,intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:1397451..1397555 32194978 MeRIP-seq:(Medium) rs117497992 Functional Loss SNV dbSNP153 33..33 33 - - - 82319 RMVar_ID_82319 Human_SNP_ID_707770610 m1A Human chrX + 1397886 1397886 1397886 GAGGAGGAGTTAGTGGGTGAACCCGGCCCGCCAGGCTGCCCTGCACAGAATTCCAGCCTTGTCAC GAGGAGGAGTTAGTGGGTGAACCCGGCCCGCCGGGCTGCCCTGCACAGAATTCCAGCCTTGTCAC A G LINC00106 Ensembl:ENSG00000236871 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1397841..1397914 26863196 MeRIP-seq:(Medium) rs1418620157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5640483,Human_RBP_ID_21997219 82320 RMVar_ID_82320 Human_SNP_ID_707770692 m1A Human chrX + 1398103 1398103 1398103 TTTGGGAGGCCGAGGCGGGGTGGATTGCCTGAAGTCAAGAGCTGAAGACCAGCCTGGCCAACATG TTTGGGAGGCCGAGGCGGGGTGGATTGCCTGAGGTCAAGAGCTGAAGACCAGCCTGGCCAACATG A G LINC00106 Ensembl:ENSG00000236871 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1398052..1398192 26863196 MeRIP-seq:(Medium) rs1206103918 Functional Loss SNV dbSNP153 33..33 33 - - - 82321 RMVar_ID_82321 Human_SNP_ID_707771043 m1A Human chrX - 1399080 1399080 1399080 CCCGTAACTGTCCCTCCTTCCTCCCTTCCCACATCAGCCTGGCCCAGAGCTGGGGCGACAGCATC CCCGTAACTGTCCCTCCTTCCTCCCTTCCCACGTCAGCCTGGCCCAGAGCTGGGGCGACAGCATC T C RF00017-6698,RF00017-4643,lnc-SLC25A6-1-001 RNACentral:URS000099749B,RNACentral:URS00009A02E8,RNACentral:URS00008B417D SRP RNA,SRP RNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1399039..1399167 26863196 MeRIP-seq:(Medium) rs1182325953 Functional Loss SNV dbSNP153 33..33 33 - - - 82322 RMVar_ID_82322 Human_SNP_ID_707772016 m1A Human chrX - 1401566 1401566 1401566 CACCCAGCTTACCTGTTCCTGGGCTGGGCGTCAGTCTCCTATATTTCAGCTGTTTTCCTTTTTCT CACCCAGCTTACCTGTTCCTGGGCTGGGCGTCTGTCTCCTATATTTCAGCTGTTTTCCTTTTTCT T A RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1401516..1401647 26863196 MeRIP-seq:(Medium) rs1425243853 Functional Loss SNV dbSNP153 33..33 33 - - - 82323 RMVar_ID_82323 Human_SNP_ID_707773086 m1A Human chrX - 1403976 1403976 1403976 ACCATCTATTCACCCATCCATCCATCACATCCATGCATCCATCTGTCCATCCACTCATCTACCTA ACCATCTATTCACCCATCCATCCATCACATCCGTGCATCCATCTGTCCATCCACTCATCTACCTA T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1403874..1404173 26863196 MeRIP-seq:(Medium) rs1225623328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220138,Human_RBP_ID_24538039 RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82324 RMVar_ID_82324 Human_SNP_ID_707773145 m1A Human chrX - 1404277 1404124 1404278 GATCTACCATCTATTCACCCATCCATCCATCCATCTCATCCATGCATCCATCTATCCATCCATTC GATCTACCATCTATTCACCCATCCATCCATC__________________________________ AGATGGATGGTTGGGTGAATAGATGGTAGATGATGGGTACGTAGGTAGATGGATGGATAGATGGATGCATGGATGAGATGGATGGGTGAATAGATGGTAGATGATGGGTAGGTAGGTAGATGAATGGATGGATAGATGGATGCATGGATGAGATG A ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1404233..1404362 26863196 MeRIP-seq:(Medium) rs1569530265 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82325 RMVar_ID_82325 Human_SNP_ID_707773409 m1A Human chrX - 1404632 1404632 1404632 CCCATCCATCCATCTCATCCATGCATCCATCTATCCGTCCATTCGTCTACCTACCTACCCATCAT CCCATCCATCCATCTCATCCATGCATCCATCTGTCCGTCCATTCGTCTACCTACCTACCCATCAT T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1404506..1404764 26863196 MeRIP-seq:(Medium) rs1169118604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219934,Human_RBP_ID_24538043,Human_RBP_ID_26834551 RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82326 RMVar_ID_82326 Human_SNP_ID_707773524 m1A Human chrX - 1404920 1404849 1404920 ATCCATGCATCCATCTATCCATCCATACATCTACCTACGTACCCATCAGCTACCATCTATTCACC ATCCATGCATCCATCTATCCATCCATACATCT_________________________________ AAGATGAATAGTTGGATGCATGGATGAGATGGATGGTTGGGTGAATAGATGGTAGCTGATGGGTACGTAGGT A ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1403732..1407670 26863196 MeRIP-seq:(Medium) rs1569530441 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_219935,Human_RBP_ID_1405160,Human_RBP_ID_24538207 RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82327 RMVar_ID_82327 Human_SNP_ID_707773695 m1A Human chrX + 1405309 1405243 1405310 TGGATGGATAGATGGATGTGATGGATGGGTGAATAGATGGTAGATGATGGATCGTTAGGTGGATG __________________________________AGATGGTAGATGATGGATCGTTAGGTGGATG CAGATGGTAGATGATGGGTACGTAGATAGATGAGTGGATGGATAGATGGATGTGATGGATGGGTGAAT C ASMTL-AS1 Ensembl:ENSG00000236017 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1405304..1405491 26863196 MeRIP-seq:(Medium) rs1569530524 Functional Loss DEL dbSNP153 1..34 33 - - - 82328 RMVar_ID_82328 Human_SNP_ID_707773712 m1A Human chrX + 1405333 1405275 1405334 ATGGGTGAATAGATGGTAGATGATGGATCGTTAGGTGGATGGATAGATGGAGGCATGGATGAGAT __________________________________GTGGATGGATAGATGGAGGCATGGATGAGAT AGTGGATGGATAGATGGATGTGATGGATGGGTGAATAGATGGTAGATGATGGATCGTTAG A ASMTL-AS1 Ensembl:ENSG00000236017 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1404846..1405420 26863196 MeRIP-seq:(Medium) rs1569530538 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5232031 82329 RMVar_ID_82329 Human_SNP_ID_707773866 m1A Human chrX + 1405630 1405614 1405630 GGTAGATGATGGGTAGGTAGATAGATGAATGGATGGATAGATGGATGCATGGATGAGATGGATGG GGTAGATGATGGGTAGG________________TGGATAGATGGATGCATGGATGAGATGGATGG GTAGATAGATGAATGGA G ASMTL-AS1 Ensembl:ENSG00000236017 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1405587..1406234 26863196 MeRIP-seq:(Medium) rs1454608177 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_5232033,Human_RBP_ID_5659490,Human_RBP_ID_24394060 82330 RMVar_ID_82330 Human_SNP_ID_707774165 m1A Human chrX - 1406314 1406311 1406315 ATCCATGAATCCATCCATCCATCTACCTACCTACCCATCATCTACCATCTATTCACCCAACCATC ATCCATGAATCCATCCATCCATCTACCTACC____CATCATCTACCATCTATTCACCCAACCATC GGGTA G ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1406305..1406565 26863196 MeRIP-seq:(Medium) rs1465921973 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82331 RMVar_ID_82331 Human_SNP_ID_707774833 m1A Human chrX + 1407832 1407831 1407833 AGATAAAGGAGGAAGGAGGAGAGAAGAGAAACAGAGATTGATGATGATAGATGAGATACCTAAAA AGATAAAGGAGGAAGGAGGAGAGAAGAGAAAC__AGATTGATGATGATAGATGAGATACCTAAAA CAG C ASMTL-AS1 Ensembl:ENSG00000236017 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1407783..1407978 26863196 MeRIP-seq:(Medium) rs748339983 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16298,Human_RBP_ID_5483592 82332 RMVar_ID_82332 Human_SNP_ID_707776623 m1A Human chrX - 1413323 1413323 1413323 CCTTGCCTTCTTGTCGCCCAGGCTGGAGTGCGATGGCGCGATCTCGGCTCACTGCAACCTCCACC CCTTGCCTTCTTGTCGCCCAGGCTGGAGTGCGGTGGCGCGATCTCGGCTCACTGCAACCTCCACC T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1413321..1413442 26863196 MeRIP-seq:(Medium) rs1462076557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_261186 82333 RMVar_ID_82333 Human_SNP_ID_707776624 m1A Human chrX - 1413323 1413323 1413323 CCTTGCCTTCTTGTCGCCCAGGCTGGAGTGCGATGGCGCGATCTCGGCTCACTGCAACCTCCACC CCTTGCCTTCTTGTCGCCCAGGCTGGAGTGCGCTGGCGCGATCTCGGCTCACTGCAACCTCCACC T G ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1413321..1413442 26863196 MeRIP-seq:(Medium) rs1462076557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_261186 82334 RMVar_ID_82334 Human_SNP_ID_707776648 m1A Human chrX + 1413364 1413364 1413364 AGCCTGGGCGACAAGAAGGCAAGGGAGGAAAAAAGCAGGGAATTCAGGGGCAGCACCTGGGCGAG AGCCTGGGCGACAAGAAGGCAAGGGAGGAAAAGAGCAGGGAATTCAGGGGCAGCACCTGGGCGAG A G ASMTL-AS1 Ensembl:ENSG00000236017 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1413353..1413458 26863196 MeRIP-seq:(Medium) rs1569531669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5640433,Human_RBP_ID_22734391,Human_RBP_ID_27574977 RMVar_hsa_circ_61447,RMVar_hsa_circ_77967,RMVar_hsa_circ_261187 82335 RMVar_ID_82335 Human_SNP_ID_707776999 m1A Human chrX + 1414168 1414168 1414168 GATGGAGGCAGAGACTGGAGTGATGCGGCTACAAGCCCAGGGACACCCGGAGCCCCCAGGAGCTG GATGGAGGCAGAGACTGGAGTGATGCGGCTACGAGCCCAGGGACACCCGGAGCCCCCAGGAGCTG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:1414006..1414435;chrX:1414058..1414382 26863196 MeRIP-seq:(Medium) rs1222837690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61447,RMVar_hsa_circ_77967,RMVar_hsa_circ_261187 82336 RMVar_ID_82336 Human_SNP_ID_707777862 m1A Human chrX - 1416158 1416156 1416158 CTGTGTGTGCCTGTCGCTATATCTGTATGTCCATGTGTGTGTGCCCATCTGTGCATGTCTGCGTC CTGTGTGTGCCTGTCGCTATATCTGTATGTCC__GTGTGTGTGCCCATCTGTGCATGTCTGCGTC CAT C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1416109..1416222 26863196 MeRIP-seq:(Medium) rs1265571530 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_261186 82337 RMVar_ID_82337 Human_SNP_ID_707777863 m1A Human chrX - 1416158 1416158 1416158 CTGTGTGTGCCTGTCGCTATATCTGTATGTCCATGTGTGTGTGCCCATCTGTGCATGTCTGCGTC CTGTGTGTGCCTGTCGCTATATCTGTATGTCCGTGTGTGTGTGCCCATCTGTGCATGTCTGCGTC T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1416109..1416222 26863196 MeRIP-seq:(Medium) rs1432597127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_261186 82338 RMVar_ID_82338 Human_SNP_ID_707777882 m1A Human chrX + 1416183 1416183 1416183 ACACACATGGACATACAGATATAGCGACAGGCACACACAGACGCAGACATGCACAGCAACAGGCA ACACACATGGACATACAGATATAGCGACAGGCGCACACAGACGCAGACATGCACAGCAACAGGCA A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1416174..1416322 26863196 MeRIP-seq:(Medium) rs1190201606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3247481 82339 RMVar_ID_82339 Human_SNP_ID_707777925 m1A Human chrX + 1416253 1416252 1416254 AGACGCAGACATGCACAGATGGGCACAGACAGACACGCACGGACACACAGATACACCAACAGACA AGACGCAGACATGCACAGATGGGCACAGACAG__ACGCACGGACACACAGATACACCAACAGACA GAC G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1416203..1416325 26863196 MeRIP-seq:(Medium) rs1163109988 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3247482 82340 RMVar_ID_82340 Human_SNP_ID_707777938 m1A Human chrX + 1416281 1416277 1416281 ACAGACACGCACGGACACACAGATACACCAACAGACAGGCACGCACACAGACGCAGACATGCACA ACAGACACGCACGGACACACAGATACACC____GACAGGCACGCACACAGACGCAGACATGCACA CAACA C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1416236..1416329 26863196 MeRIP-seq:(Medium) rs1255306778 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3247482 82341 RMVar_ID_82341 Human_SNP_ID_707777940 m1A Human chrX + 1416281 1416278 1416282 ACAGACACGCACGGACACACAGATACACCAACAGACAGGCACGCACACAGACGCAGACATGCACA ACAGACACGCACGGACACACAGATACACCA____ACAGGCACGCACACAGACGCAGACATGCACA AACAG A RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1416236..1416329 26863196 MeRIP-seq:(Medium) rs1288829769 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3247482 82342 RMVar_ID_82342 Human_SNP_ID_707778071 m1A Human chrX + 1416437 1416432 1416438 ACAGATACACCAACAGACAGGCACACGCACATAAACATAGACATGCACAGATGGACACGCAGACA ACAGATACACCAACAGACAGGCACACGC______ACATAGACATGCACAGATGGACACGCAGACA CACATAA C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1416434..1416578 26863196 MeRIP-seq:(Medium) rs1341514422 Functional Loss DEL dbSNP153 29..34 33 - - - 82343 RMVar_ID_82343 Human_SNP_ID_707778073 m1A Human chrX + 1416437 1416434 1416438 ACAGATACACCAACAGACAGGCACACGCACATAAACATAGACATGCACAGATGGACACGCAGACA ACAGATACACCAACAGACAGGCACACGCAC____ACATAGACATGCACAGATGGACACGCAGACA CATAA C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1416434..1416578 26863196 MeRIP-seq:(Medium) rs1217554021 Functional Loss DEL dbSNP153 31..34 33 - - - 82344 RMVar_ID_82344 Human_SNP_ID_707778080 m1A Human chrX + 1416437 1416437 1416437 ACAGATACACCAACAGACAGGCACACGCACATAAACATAGACATGCACAGATGGACACGCAGACA ACAGATACACCAACAGACAGGCACACGCACATGAACATAGACATGCACAGATGGACACGCAGACA A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1416434..1416578 26863196 MeRIP-seq:(Medium) rs867969192 Functional Loss SNV dbSNP153 33..33 33 - - - 82345 RMVar_ID_82345 Human_SNP_ID_707778501 m1A Human chrX + 1417068 1417065 1417069 CACAAGCACAGCAGATGCTCACATATCCACACAGACACACACCATGCACATAGATGCAGACACAC CACAAGCACAGCAGATGCTCACATATCCAC____ACACACACCATGCACATAGATGCAGACACAC CACAG C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1417046..1417320 26863196 MeRIP-seq:(Medium) rs1409113604 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3247524 82346 RMVar_ID_82346 Human_SNP_ID_707778505 m1A Human chrX + 1417070 1417070 1417070 CAAGCACAGCAGATGCTCACATATCCACACAGACACACACCATGCACATAGATGCAGACACACAG CAAGCACAGCAGATGCTCACATATCCACACAGTCACACACCATGCACATAGATGCAGACACACAG A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1417061..1417182 26863196 MeRIP-seq:(Medium) rs745319081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3247524 82347 RMVar_ID_82347 Human_SNP_ID_707779051 m1A Human chrX - 1418036 1418036 1418036 TGCAGGTGACTGTGTTTGACCTCCCAGACATTATCGAGCTGGCCGCCCACTTCCAACCCCCCGGA TGCAGGTGACTGTGTTTGACCTCCCAGACATTCTCGAGCTGGCCGCCCACTTCCAACCCCCCGGA T G ASMTL Ensembl:ENSG00000169093 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1417928..1418036 26863196 MeRIP-seq:(Medium) rs764030032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182701,Human_Splice_Rec_2182716,Human_Splice_Rec_2182717 RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_26076,RMVar_hsa_circ_261186,RMVar_hsa_circ_62617 82348 RMVar_ID_82348 Human_SNP_ID_707780091 m1A Human chrX - 1420306 1420293 1420307 AGAGATGGAGGCAGACAGAGACAGGGAGATAGAGGGAGACAGAAACAGGGAGACAGAAAGACAGA AGAGATGGAGGCAGACAGAGACAGGGAGATA______________CAGGGAGACAGAAAGACAGA GTTTCTGTCTCCCTC G ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:1420293..1420385 26863196 MeRIP-seq:(Medium) rs1233057895 Functional Loss DEL dbSNP153 32..45 33 - - - RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_114559,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_261186,RMVar_hsa_circ_62617 82349 RMVar_ID_82349 Human_SNP_ID_707780653 m1A Human chrX - 1421844 1421844 1421844 TTAGGAGGTCACACGACTGTCCCCATTTCTCCAGGTTACAGTAACACAGAGACAGCGAACGTCTA TTAGGAGGTCACACGACTGTCCCCATTTCTCCGGGTTACAGTAACACAGAGACAGCGAACGTCTA T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:1421795..1431938 32194978 MeRIP-seq:(Medium) rs752060478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4744,RMVar_hsa_circ_10428,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_62617,RMVar_hsa_circ_70387,RMVar_hsa_circ_314718,RMVar_hsa_circ_50643 82350 RMVar_ID_82350 Human_SNP_ID_707781394 m1A Human chrX + 1424264 1424264 1424264 GCACCCGTCCATCCATTCATGCACTCATCCACATGCCCACTCATCCATCCACCCATCCAACCACC GCACCCGTCCATCCATTCATGCACTCATCCACTTGCCCACTCATCCATCCACCCATCCAACCACC A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1424262..1424345 26863196 MeRIP-seq:(Medium) rs1170171015 Functional Loss SNV dbSNP153 33..33 33 - - - 82351 RMVar_ID_82351 Human_SNP_ID_707782606 m1A Human chrX - 1427840 1427832 1427841 GGGCAGCCGCGATGAGAAGGCCGAGGCGGGAGAGGCGGGACAGGCCACGGCAGAGGCTGAGTGTC GGGCAGCCGCGATGAGAAGGCCGAGGCGGGA_________CAGGCCACGGCAGAGGCTGAGTGTC GTCCCGCCTC G ASMTL Ensembl:ENSG00000169093 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1427796..1427950 26863196 MeRIP-seq:(Medium) rs747702844 Functional Loss DEL dbSNP153 32..40 33 - - - Human_miRNA_ID_2027743,Human_miRNA_ID_2225921 RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_293294,RMVar_hsa_circ_34978,RMVar_hsa_circ_62617,RMVar_hsa_circ_70387,RMVar_hsa_circ_314718,RMVar_hsa_circ_5630,RMVar_hsa_circ_268218 82352 RMVar_ID_82352 Human_SNP_ID_707784109 m1A Human chrX - 1431934 1431934 1431934 CCCAGAGGTCTGTGCCCAGGACGCTGGCTGCAATTAACACGAATAAACTCTGTGATCCAAAGTCA CCCAGAGGTCTGTGCCCAGGACGCTGGCTGCAGTTAACACGAATAAACTCTGTGATCCAAAGTCA T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1431931..1432109 26863196 MeRIP-seq:(Medium) rs1308391399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8226444,Human_RBP_ID_9443120 RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_34978,RMVar_hsa_circ_70387,RMVar_hsa_circ_5630 82353 RMVar_ID_82353 Human_SNP_ID_707790058 m1A Human chrX - 1448023 1448023 1448023 TGGTTCTTATCCAAGATGGCGGTGTGTGTCCAAGATGGTGTGTGTCCAAGATGGTGGTTCTTATC TGGTTCTTATCCAAGATGGCGGTGTGTGTCCAGGATGGTGTGTGTCCAAGATGGTGGTTCTTATC T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1448005..1448207 26863196 MeRIP-seq:(Medium) rs1415768761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82354 RMVar_ID_82354 Human_SNP_ID_707790739 m1A Human chrX + 1449957 1449956 1449958 TAACTAACCCCCACCACCAGTAAATATGCCCCATCATCACCAGTAACTATCCCTCATCACCGGTA TAACTAACCCCCACCACCAGTAAATATGCCCC__CATCACCAGTAACTATCCCTCATCACCGGTA CAT C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:1449954..1450100;chrX:1449954..1450067 26863196 MeRIP-seq:(Medium) rs1445307466 Functional Loss DEL dbSNP153 33..34 33 - - - 82355 RMVar_ID_82355 Human_SNP_ID_707790740 m1A Human chrX + 1449957 1449957 1449957 TAACTAACCCCCACCACCAGTAAATATGCCCCATCATCACCAGTAACTATCCCTCATCACCGGTA TAACTAACCCCCACCACCAGTAAATATGCCCCGTCATCACCAGTAACTATCCCTCATCACCGGTA A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:1449954..1450100;chrX:1449954..1450067 26863196 MeRIP-seq:(Medium) rs772458332 Functional Loss SNV dbSNP153 33..33 33 - - - 82356 RMVar_ID_82356 Human_SNP_ID_707791342 m1A Human chrX + 1451135 1451135 1451135 CCTAGGCGGTCCTGGATCACTCTCCCCTCCCCATTCCTAGGGGGTCCTGGGACACTCCTCCCTCC CCTAGGCGGTCCTGGATCACTCTCCCCTCCCCCTTCCTAGGGGGTCCTGGGACACTCCTCCCTCC A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1451132..1451266 26863196 MeRIP-seq:(Medium) rs1391629196 Functional Loss SNV dbSNP153 33..33 33 - - - 82357 RMVar_ID_82357 Human_SNP_ID_707791452 m1A Human chrX - 1451344 1451344 1451344 GAAGGGTGACCCGGGACCCCCAAGGAATGGGGAGGGGAGAGTGACCCAGGACCACCTAGGGATGG GAAGGGTGACCCGGGACCCCCAAGGAATGGGGGGGGGAGAGTGACCCAGGACCACCTAGGGATGG T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1451339..1451415 26863196 MeRIP-seq:(Medium) rs1469455765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930538 RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82358 RMVar_ID_82358 Human_SNP_ID_707791689 m1A Human chrX - 1451798 1451798 1451798 AACCCGGGACCCCCAGGCATGGGGATGGGGAGAGTAACCCGGGACCTCCAGGGTTGGGGATAGGG AACCCGGGACCCCCAGGCATGGGGATGGGGAGCGTAACCCGGGACCTCCAGGGTTGGGGATAGGG T G ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1451795..1451993 26863196 MeRIP-seq:(Medium) rs1194460680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98632,RMVar_hsa_circ_261185 82359 RMVar_ID_82359 Human_SNP_ID_707792168 m1A Human chrX + 1452820 1452820 1452820 GCCAGCACCACGCGCTTGTGCAGCAGCTTCCCAATCACCGGGCACAGCACCATGGCGTCCACGCC GCCAGCACCACGCGCTTGTGCAGCAGCTTCCCGATCACCGGGCACAGCACCATGGCGTCCACGCC A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1452687..1452826 26863196 MeRIP-seq:(Medium) rs368464963 Functional Loss SNV dbSNP153 33..33 33 - - - 82360 RMVar_ID_82360 Human_SNP_ID_707792673 m1A Human chrX + 1453645 1453645 1453645 CTTACCCGCACGTGGAGGGGCCCGGCGCAGAGATGGGGGTCTTGTGGGAGCCGCGTCGGGGAAGG CTTACCCGCACGTGGAGGGGCCCGGCGCAGAGTTGGGGGTCTTGTGGGAGCCGCGTCGGGGAAGG A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1453629..1453725 26863196 MeRIP-seq:(Medium) rs1338088076 Functional Loss SNV dbSNP153 33..33 33 - - - 82361 RMVar_ID_82361 Human_SNP_ID_707837283 m1A Human chrX - 1591662 1591662 1591662 GGACAGGCGCGGCCTCACCGCCGGGAGCCGCCACCGTCCCCCGGAGGCGCCTCCGACGCCGCCAC GGACAGGCGCGGCCTCACCGCCGGGAGCCGCCGCCGTCCCCCGGAGGCGCCTCCGACGCCGCCAC T C RF00017-4643,RF00017-4501 RNACentral:URS00009A02E8,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:1591601..1593525;chrX:1591601..1593962 26863196 MeRIP-seq:(Medium) rs1453286317 Functional Loss SNV dbSNP153 33..33 33 - - - 82362 RMVar_ID_82362 Human_SNP_ID_707837289 m1A Human chrX - 1591669 1591669 1591669 GATCCCCGGACAGGCGCGGCCTCACCGCCGGGAGCCGCCACCGTCCCCCGGAGGCGCCTCCGACG GATCCCCGGACAGGCGCGGCCTCACCGCCGGGTGCCGCCACCGTCCCCCGGAGGCGCCTCCGACG T A RF00017-4643,RF00017-4501 RNACentral:URS00009A02E8,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:1591621..1591825 26863196 MeRIP-seq:(Medium) rs1456110895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7990174 82363 RMVar_ID_82363 Human_SNP_ID_707837320 m1A Human chrX - 1591771 1591771 1591771 AGCCAGGCCCGGGAGGCACGGGGGCGGCACTCACCTGCGCGGGGCTCCGCCTGCGTCCCAGGCCG AGCCAGGCCCGGGAGGCACGGGGGCGGCACTCGCCTGCGCGGGGCTCCGCCTGCGTCCCAGGCCG T C RF00017-4643,RF00017-4501 RNACentral:URS00009A02E8,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:1591675..1591819 26863410 MeRIP-seq:(Medium) rs1490785966 Functional Loss SNV dbSNP153 33..33 33 - - - 82364 RMVar_ID_82364 Human_SNP_ID_707938290 m1A Human chrX - 1894526 1894526 1894526 AGCAGAGAGACAGGGAGGCAGAGACAGAGAGAAGCAGAGAGAGAGACAGAGGCAGAGAGAGAGAC AGCAGAGAGACAGGGAGGCAGAGACAGAGAGAGGCAGAGAGAGAGACAGAGGCAGAGAGAGAGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:1894489..1894554 26863196 MeRIP-seq:(Medium) rs1444794656 Functional Loss SNV dbSNP153 33..33 33 - - - 82365 RMVar_ID_82365 Human_SNP_ID_707956941 m1A Human chrX + 2138716 2138716 2138716 CATTTTCTCCCCCCGCCCCCCCCCCCGCCCCCACTGGAAGAACTTGTTGTCCAGAACAAGTGTAG CATTTTCTCCCCCCGCCCCCCCCCCCGCCCCCCCTGGAAGAACTTGTTGTCCAGAACAAGTGTAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:2138676..2138725 26863196 MeRIP-seq:(Medium) rs1457397773 Functional Loss SNV dbSNP153 33..33 33 - - - 82366 RMVar_ID_82366 Human_SNP_ID_707967203 m1A Human chrX + 2180402 2180399 2180403 ATGTAGCCCATCTATCCTTTATCTGTCTGCCTATCTATATCTATCTGCCTATCGTCATCTACGTA ATGTAGCCCATCTATCCTTTATCTGTCTGC____CTATATCTATCTGCCTATCGTCATCTACGTA CCTAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:2180391..2180512 26863196 MeRIP-seq:(Medium) rs1254672769 Functional Loss DEL dbSNP153 31..34 33 - - - 82367 RMVar_ID_82367 Human_SNP_ID_707968071 m1A Human chrX - 2184140 2184140 2184140 ATGGATAGATAGATGATGGTGATGATATAGTTAGACACGTGATGGTGATAACAGATGATGATGGT ATGGATAGATAGATGATGGTGATGATATAGTTGGACACGTGATGGTGATAACAGATGATGATGGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:2184132..2184236 26863196 MeRIP-seq:(Medium) rs1178806313 Functional Loss SNV dbSNP153 33..33 33 - - - 82368 RMVar_ID_82368 Human_SNP_ID_707978751 m1A Human chrX - 2221159 2221159 2221159 AGTCACCCCAGAGCTGGAAGGAGTTGGTGGCCATTACCTATACAACGAGAAAGAGACCAAGTCCC AGTCACCCCAGAGCTGGAAGGAGTTGGTGGCCGTTACCTATACAACGAGAAAGAGACCAAGTCCC T C DHRSX Ensembl:ENSG00000169084 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3210910 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17667224 82369 RMVar_ID_82369 Human_SNP_ID_707982082 m1A Human chrX - 2231900 2231894 2231900 GAGAAAGATAGAGGAAAAGAAGAAGATAAGAGAAAGAGGAGGAGGAGGAAGAAGTTGGAGAAGAT GAGAAAGATAGAGGAAAAGAAGAAGATAAGAG______GAGGAGGAGGAAGAAGTTGGAGAAGAT CCTCTTT C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2231896..2232136 26863196 MeRIP-seq:(Medium) rs997404546 Functional Loss DEL dbSNP153 33..38 33 - - - 82370 RMVar_ID_82370 Human_SNP_ID_707982089 m1A Human chrX - 2231900 2231900 2231900 GAGAAAGATAGAGGAAAAGAAGAAGATAAGAGAAAGAGGAGGAGGAGGAAGAAGTTGGAGAAGAT GAGAAAGATAGAGGAAAAGAAGAAGATAAGAGGAAGAGGAGGAGGAGGAAGAAGTTGGAGAAGAT T C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2231896..2232136 26863196 MeRIP-seq:(Medium) rs1004661145 Functional Loss SNV dbSNP153 33..33 33 - - - 82371 RMVar_ID_82371 Human_SNP_ID_708012253 m1A Human chrX - 2339531 2339531 2339531 GGGACTTGGGGAGAGCTTGGGAGGGGGCAGCGAGGGATAAAAGACTACAAATAGTGTGGAATGTG GGGACTTGGGGAGAGCTTGGGAGGGGGCAGCGTGGGATAAAAGACTACAAATAGTGTGGAATGTG T A DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2339528..2339598 26863196 MeRIP-seq:(Medium) rs1010873485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94176,RMVar_hsa_circ_261193,RMVar_hsa_circ_341978,RMVar_hsa_circ_272633,RMVar_hsa_circ_261195,RMVar_hsa_circ_261196,RMVar_hsa_circ_303132,RMVar_hsa_circ_261198,RMVar_hsa_circ_64779 82372 RMVar_ID_82372 Human_SNP_ID_708021170 m1A Human chrX - 2371439 2371436 2371439 TGGTAACGAGGAGGGACTATAGTAACGAAAGGAGGGTCTGTGGTAACAGAAGGAGGGACTATGGT TGGTAACGAGGAGGGACTATAGTAACGAAAGG___GTCTGTGGTAACAGAAGGAGGGACTATGGT CCCT C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:2371434..2371609 26863196 MeRIP-seq:(Medium) rs1379802689 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3930557,Human_RBP_ID_8226461,Human_RBP_ID_22734396 RMVar_hsa_circ_94176,RMVar_hsa_circ_261193,RMVar_hsa_circ_341978,RMVar_hsa_circ_272633,RMVar_hsa_circ_261195,RMVar_hsa_circ_261196,RMVar_hsa_circ_303132,RMVar_hsa_circ_261198,RMVar_hsa_circ_64779 82373 RMVar_ID_82373 Human_SNP_ID_708021224 m1A Human chrX - 2371566 2371544 2371566 CTGCTAATGGGAGGAGGTACTATGGTAATGGAAGGAGGGACTATGGTAACAGAAGGACGGACTAT CTGCTAATGGGAGGAGGTACTATGGTAATGGA______________________GGACGGACTAT CTTCTGTTACCATAGTCCCTCCT C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:2371371..2371687 26863196 MeRIP-seq:(Medium) rs1434225464 Functional Loss DEL dbSNP153 33..54 33 - - - RMVar_hsa_circ_94176,RMVar_hsa_circ_261193,RMVar_hsa_circ_341978,RMVar_hsa_circ_272633,RMVar_hsa_circ_261195,RMVar_hsa_circ_261196,RMVar_hsa_circ_303132,RMVar_hsa_circ_261198,RMVar_hsa_circ_64779 82374 RMVar_ID_82374 Human_SNP_ID_708023918 m1A Human chrX - 2382681 2382681 2382681 TGATGGTGATGGTGATGATGGTGATGATGGTGATGGTGATGATGATGGTGATGATGGTGGTGATG TGATGGTGATGGTGATGATGGTGATGATGGTGGTGGTGATGATGATGGTGATGATGGTGGTGATG T C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:2382451..2382743;chrX:2382459..2382737 26863196 MeRIP-seq:(Medium) rs1295945195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94176,RMVar_hsa_circ_261193,RMVar_hsa_circ_341978,RMVar_hsa_circ_272633,RMVar_hsa_circ_261195,RMVar_hsa_circ_261196,RMVar_hsa_circ_303132,RMVar_hsa_circ_261198,RMVar_hsa_circ_64779 82375 RMVar_ID_82375 Human_SNP_ID_708031642 m1A Human chrX - 2413893 2413893 2413893 GTCATGTTGAGGTTTATTTGGGCTAGGTTATAATGAGATTTAGTTGGGTTAGGTCATGATGAGGT GTCATGTTGAGGTTTATTTGGGCTAGGTTATAGTGAGATTTAGTTGGGTTAGGTCATGATGAGGT T C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2413891..2414471 26863196 MeRIP-seq:(Medium) rs1166349699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94176,RMVar_hsa_circ_261193,RMVar_hsa_circ_341978,RMVar_hsa_circ_272633,RMVar_hsa_circ_261195,RMVar_hsa_circ_261196,RMVar_hsa_circ_303132,RMVar_hsa_circ_261198,RMVar_hsa_circ_261202,RMVar_hsa_circ_261200,RMVar_hsa_circ_286513,RMVar_hsa_circ_100120,RMVar_hsa_circ_270001,RMVar_hsa_circ_261201 82376 RMVar_ID_82376 Human_SNP_ID_708034401 m1A Human chrX - 2426397 2426396 2426398 AAGGAAGGAATGAAGGAAGAAAGGAAAAAGAGAAGGAAGGAGGAAGGAAGGAAAGAGGGAAGGAA AAGGAAGGAATGAAGGAAGAAAGGAAAAAGA__AGGAAGGAGGAAGGAAGGAAAGAGGGAAGGAA TTC T DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2426395..2426871 26863196 MeRIP-seq:(Medium) rs748833885 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_94176,RMVar_hsa_circ_261196,RMVar_hsa_circ_261202,RMVar_hsa_circ_100120,RMVar_hsa_circ_92557,RMVar_hsa_circ_261203 82377 RMVar_ID_82377 Human_SNP_ID_708055588 m1A Human chrX - 2500387 2500387 2500387 CAGGCGGCTCTGCCTGCCGCCTGCGGTCGGCCAGTGACCGCGCGCCCCCGCCAGGCCCCGGAGGG CAGGCGGCTCTGCCTGCCGCCTGCGGTCGGCCGGTGACCGCGCGCCCCCGCCAGGCCCCGGAGGG T C ZBED1,DHRSX Ensembl:ENSG00000214717,Ensembl:ENSG00000169084 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chrX:2500354..2500600;chrX:2500369..2500612 26863196 MeRIP-seq:(Medium) rs1218939196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16044,Human_RBP_ID_5076458 RMVar_hsa_circ_94176,RMVar_hsa_circ_261196,RMVar_hsa_circ_261202,RMVar_hsa_circ_100120,RMVar_hsa_circ_92557,RMVar_hsa_circ_261203 82378 RMVar_ID_82378 Human_SNP_ID_708055623 m1A Human chrX + 2500478 2500478 2500478 CCCCGGGTCCCCGGCCATGGCCCGGAGGTGTCAGGGTGCGCGGGGGGGCGGCTGCACGGGGGCTG CCCCGGGTCCCCGGCCATGGCCCGGAGGTGTCGGGGTGCGCGGGGGGGCGGCTGCACGGGGGCTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:2490721..2502805 26863196 MeRIP-seq:(Medium) rs1457607645 Functional Loss SNV dbSNP153 33..33 33 - - - 82379 RMVar_ID_82379 Human_SNP_ID_708055702 m1A Human chrX + 2500591 2500591 2500591 GAGGGAAGGGTCGGGCCGGGTCGGGCCGGGCCAGGCGCGCAGAAGAGCCGGCGGGGACGGAAAGC GAGGGAAGGGTCGGGCCGGGTCGGGCCGGGCCGGGCGCGCAGAAGAGCCGGCGGGGACGGAAAGC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:2500358..2500818 26863410 MeRIP-seq:(Medium) rs770164905 Functional Loss SNV dbSNP153 33..33 33 - - - 82380 RMVar_ID_82380 Human_SNP_ID_708056213 m1A Human chrX - 2501800 2501800 2501800 CGGGGGGTGGTTGTGATGGAGGTGGAGGTCCTAGAAGGGGGCCCCAGTAGGGGTCTGTGATCCTG CGGGGGGTGGTTGTGATGGAGGTGGAGGTCCTCGAAGGGGGCCCCAGTAGGGGTCTGTGATCCTG T G DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:2501763..2501931 26863196 MeRIP-seq:(Medium) rs1192030324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930247,Human_RBP_ID_8164700 82381 RMVar_ID_82381 Human_SNP_ID_708056450 m1A Human chrX + 2502733 2502733 2502733 GACCTTCACCCCACCACAACCCTCCCAGTCCCACACCTGGTCCCCCAGGGGACCCCAGACCTGGC GACCTTCACCCCACCACAACCCTCCCAGTCCCGCACCTGGTCCCCCAGGGGACCCCAGACCTGGC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2502718..2502795 26863196 MeRIP-seq:(Medium) rs776194979 Functional Loss SNV dbSNP153 33..33 33 - - - 82382 RMVar_ID_82382 Human_SNP_ID_708056451 m1A Human chrX + 2502733 2502733 2502733 GACCTTCACCCCACCACAACCCTCCCAGTCCCACACCTGGTCCCCCAGGGGACCCCAGACCTGGC GACCTTCACCCCACCACAACCCTCCCAGTCCCTCACCTGGTCCCCCAGGGGACCCCAGACCTGGC A T RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2502718..2502795 26863196 MeRIP-seq:(Medium) rs776194979 Functional Loss SNV dbSNP153 33..33 33 - - - 82383 RMVar_ID_82383 Human_SNP_ID_708080744 m1A Human chrX - 2606926 2606926 2606926 ACGAATGGATGGATGGATAGATAAGTGGACAGACGGATAGATAGCTGGATAGATGGGTGGGTAGA ACGAATGGATGGATGGATAGATAAGTGGACAGGCGGATAGATAGCTGGATAGATGGGTGGGTAGA T C lnc-DHRSX-1,lnc-DHRSX-3,lnc-DHRSX-1:2,lnc-DHRSX-1:3,lnc-DHRSX-1:4,lnc-DHRSX-1:5,lnc-DHRSX-1:6,lnc-DHRSX-1:7,lnc-DHRSX-1:8 RNACentral:URS0000D5D9A4,RNACentral:URS00008BC464,RNACentral:URS0000E5A87A,RNACentral:URS0000D5A104,RNACentral:URS0000E4D123,RNACentral:URS0000E35DB3,RNACentral:URS00008B6312,RNACentral:URS0000D5B12C,RNACentral:URS0000D592A4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2606826..2607034 26863196 MeRIP-seq:(Medium) rs1330673491 Functional Loss SNV dbSNP153 33..33 33 - - - 82384 RMVar_ID_82384 Human_SNP_ID_708080854 m1A Human chrX - 2607193 2607190 2607193 TAAATGGACAGATGAATAAATGGATGGATGAAAGGGGGGATAGACGGATTGATCTATGGATAGAT TAAATGGACAGATGAATAAATGGATGGATGAA___GGGGATAGACGGATTGATCTATGGATAGAT CCCT C lnc-DHRSX-1,lnc-DHRSX-3,lnc-DHRSX-1:2,lnc-DHRSX-1:3,lnc-DHRSX-1:4,lnc-DHRSX-1:5,lnc-DHRSX-1:6,lnc-DHRSX-1:7,lnc-DHRSX-1:8 RNACentral:URS0000D5D9A4,RNACentral:URS00008BC464,RNACentral:URS0000E5A87A,RNACentral:URS0000D5A104,RNACentral:URS0000E4D123,RNACentral:URS0000E35DB3,RNACentral:URS00008B6312,RNACentral:URS0000D5B12C,RNACentral:URS0000D592A4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2607091..2607532 26863196 MeRIP-seq:(Medium) rs1021409639 Functional Loss DEL dbSNP153 33..35 33 - - - 82385 RMVar_ID_82385 Human_SNP_ID_708080857 m1A Human chrX - 2607193 2607192 2607193 TAAATGGACAGATGAATAAATGGATGGATGAAAGGGGGGATAGACGGATTGATCTATGGATAGAT TAAATGGACAGATGAATAAATGGATGGATGAA_GGGGGGATAGACGGATTGATCTATGGATAGAT CT C lnc-DHRSX-1,lnc-DHRSX-3,lnc-DHRSX-1:2,lnc-DHRSX-1:3,lnc-DHRSX-1:4,lnc-DHRSX-1:5,lnc-DHRSX-1:6,lnc-DHRSX-1:7,lnc-DHRSX-1:8 RNACentral:URS0000D5D9A4,RNACentral:URS00008BC464,RNACentral:URS0000E5A87A,RNACentral:URS0000D5A104,RNACentral:URS0000E4D123,RNACentral:URS0000E35DB3,RNACentral:URS00008B6312,RNACentral:URS0000D5B12C,RNACentral:URS0000D592A4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2607091..2607532 26863196 MeRIP-seq:(Medium) rs1397191751 Functional Loss DEL dbSNP153 33..33 33 - - - 82386 RMVar_ID_82386 Human_SNP_ID_708080861 m1A Human chrX - 2607208 2607208 2607208 GGGTGGAGGAATGGATAAATGGACAGATGAATAAATGGATGGATGAAAGGGGGGATAGACGGATT GGGTGGAGGAATGGATAAATGGACAGATGAATGAATGGATGGATGAAAGGGGGGATAGACGGATT T C lnc-DHRSX-1,lnc-DHRSX-3,lnc-DHRSX-1:2,lnc-DHRSX-1:3,lnc-DHRSX-1:4,lnc-DHRSX-1:5,lnc-DHRSX-1:6,lnc-DHRSX-1:7,lnc-DHRSX-1:8 RNACentral:URS0000D5D9A4,RNACentral:URS00008BC464,RNACentral:URS0000E5A87A,RNACentral:URS0000D5A104,RNACentral:URS0000E4D123,RNACentral:URS0000E35DB3,RNACentral:URS00008B6312,RNACentral:URS0000D5B12C,RNACentral:URS0000D592A4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:2607099..2607443 26863196 MeRIP-seq:(Medium) rs192340074 Functional Loss SNV dbSNP153 33..33 33 - - - 82387 RMVar_ID_82387 Human_SNP_ID_708091457 m1A Human chrX + 2649991 2649991 2649991 ATATTTGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGAGTGAATGGCTGAGTGGA ATATTTGGATGGATGGATGGATGGATGGATGGGTGGATGGATGGATGAGTGAATGGCTGAGTGGA A G CD99P1 Ensembl:ENSG00000223773 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:2649874..2650156 26863196 MeRIP-seq:(Medium) rs867366803 Functional Loss SNV dbSNP153 33..33 33 - - - 82388 RMVar_ID_82388 Human_SNP_ID_708102584 m1A Human chrX - 2691386 2691386 2691386 CGACCAGAACACCCAGCAGGCCGAAGAGCAGCAGCGCCAGCGCAGCCCCGCGGGCCATGGTGCGC CGACCAGAACACCCAGCAGGCCGAAGAGCAGCGGCGCCAGCGCAGCCCCGCGGGCCATGGTGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:2691201..2691482 26863196 MeRIP-seq:(Medium) rs1252163150 Functional Loss SNV dbSNP153 33..33 33 - - - 82389 RMVar_ID_82389 Human_SNP_ID_708102585 m1A Human chrX - 2691389 2691389 2691389 CGGCGACCAGAACACCCAGCAGGCCGAAGAGCAGCAGCGCCAGCGCAGCCCCGCGGGCCATGGTG CGGCGACCAGAACACCCAGCAGGCCGAAGAGCGGCAGCGCCAGCGCAGCCCCGCGGGCCATGGTG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chrX:2691212..2691401;chrX:2691176..2691462 26863410 MeRIP-seq:(Medium) rs759552988 Functional Loss SNV dbSNP153 33..33 33 - - - 82390 RMVar_ID_82390 Human_SNP_ID_708102616 m1A Human chrX - 2691429 2691429 2691429 GCGTCCCCCAACCCGGATCCCTCCGCTCGCTCACCCGGGGCGGCGACCAGAACACCCAGCAGGCC GCGTCCCCCAACCCGGATCCCTCCGCTCGCTCCCCCGGGGCGGCGACCAGAACACCCAGCAGGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:2691251..2691460;chrX:2691201..2691549;chrX:2691226..2691599;chrX:2691326..2691549;chrX:2691301..2691450 26863196,32194978,32194978 MeRIP-seq:(Medium) rs969790002 Functional Loss SNV dbSNP153 33..33 33 - - - 82391 RMVar_ID_82391 Human_SNP_ID_708108702 m1A Human chrX - 2714404 2714404 2714404 AATCGAAACCACCATCTAAGAGAGAAAAAAAGAGTCAACTTAGAAACAAGAAAAATAAAAATAAA AATCGAAACCACCATCTAAGAGAGAAAAAAAGGGTCAACTTAGAAACAAGAAAAATAAAAATAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:2714401..2714475 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1464317713 Functional Loss SNV dbSNP153 33..33 33 - - - 82392 RMVar_ID_82392 Human_SNP_ID_708109708 m1A Human chrX + 2717605 2717605 2717605 CTTTTACTAACTGAAATATCTTATCTCTTTAGACAATGAAAACAAGAAACCCACTGCAATCCCCA CTTTTACTAACTGAAATATCTTATCTCTTTAGGCAATGAAAACAAGAAACCCACTGCAATCCCCA A G CD99 Ensembl:ENSG00000002586 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:2717601..2717675;chrX:2717601..2717650;chrX:2717601..2717625 26863196 MeRIP-seq:(Medium) rs752820716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17203380 Human_Splice_Rec_2182826,Human_Splice_Rec_2182827,Human_Splice_Rec_2182850,Human_Splice_Rec_2182851,Human_Splice_Rec_2182861,Human_Splice_Rec_2182864,Human_Splice_Rec_2182870,Human_Splice_Rec_2182881,Human_Splice_Rec_2182895,Human_Splice_Rec_2182896,Human_Splice_Rec_2182910,Human_Splice_Rec_2182922,Human_Splice_Rec_2182932,Human_Splice_Rec_2182933 RMVar_hsa_circ_50939,RMVar_hsa_circ_337905,RMVar_hsa_circ_40997,RMVar_hsa_circ_261209 82393 RMVar_ID_82393 Human_SNP_ID_708110367 m1A Human chrX + 2720354 2720354 2720354 ACTTAAAATTGCAACTCTCATCTTTCACAAACAGACGACCCACGACCACCGAACCCACCCAAACC ACTTAAAATTGCAACTCTCATCTTTCACAAACTGACGACCCACGACCACCGAACCCACCCAAACC A T CD99 Ensembl:ENSG00000002586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:2720351..2720400;chrX:2720351..2720425 26863196 MeRIP-seq:(Medium) rs1260514225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24394088,Human_RBP_ID_27551442 Human_Splice_Rec_2182831,Human_Splice_Rec_2182842,Human_Splice_Rec_2182853,Human_Splice_Rec_2182866,Human_Splice_Rec_2182872,Human_Splice_Rec_2182885,Human_Splice_Rec_2182899,Human_Splice_Rec_2182913,Human_Splice_Rec_2182924,Human_Splice_Rec_2182937,Human_Splice_Rec_2182944 RMVar_hsa_circ_261210,RMVar_hsa_circ_50939,RMVar_hsa_circ_337905,RMVar_hsa_circ_40997,RMVar_hsa_circ_261209,RMVar_hsa_circ_325543,RMVar_hsa_circ_372135,RMVar_hsa_circ_261211,RMVar_hsa_circ_115994,RMVar_hsa_circ_347096 82394 RMVar_ID_82394 Human_SNP_ID_708116080 m1A Human chrX + 2740808 2740808 2740808 CAGTTCAGCGTACTCTTTTAGAGAAATAGAAGATTGTCGGCAGAAACAGCCCAGGCGTTGGCAGC CAGTTCAGCGTACTCTTTTAGAGAAATAGAAGGTTGTCGGCAGAAACAGCCCAGGCGTTGGCAGC A G CD99 Ensembl:ENSG00000002586 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:2738189..2740812 32194978 MeRIP-seq:(Medium) rs368583318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1714447,Human_RBP_ID_5124582,Human_RBP_ID_5637585,Human_RBP_ID_8718041,Human_RBP_ID_17667233,Human_RBP_ID_24394247 Human_Splice_Rec_2182904,Human_Splice_Rec_2182950 82395 RMVar_ID_82395 Human_SNP_ID_708135572 m1A Human chrX + 2829255 2829255 2829255 GAGGGGAGGGGTGCGGGGCGCGGGAGTAGGCCAGGAGCGCTTAGGGGTGAGTGCGCCGAGCCAGG GAGGGGAGGGGTGCGGGGCGCGGGAGTAGGCCTGGAGCGCTTAGGGGTGAGTGCGCCGAGCCAGG A T GYG2 Ensembl:ENSG00000056998 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:2829204..2829486 26863196 MeRIP-seq:(Medium) rs1183589872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268979,Human_RBP_ID_848283,Human_RBP_ID_3930250,Human_RBP_ID_5330649,Human_RBP_ID_8226468,Human_RBP_ID_8944843,Human_RBP_ID_9443139,Human_RBP_ID_18963402 Human_Splice_Rec_2183045 82396 RMVar_ID_82396 Human_SNP_ID_708135575 m1A Human chrX + 2829265 2829265 2829265 GTGCGGGGCGCGGGAGTAGGCCAGGAGCGCTTAGGGGTGAGTGCGCCGAGCCAGGGCACCGAGTG GTGCGGGGCGCGGGAGTAGGCCAGGAGCGCTTGGGGGTGAGTGCGCCGAGCCAGGGCACCGAGTG A G GYG2 Ensembl:ENSG00000056998 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:2828810..2829992 26863196 MeRIP-seq:(Medium) rs1211249053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268979,Human_RBP_ID_3930250,Human_RBP_ID_5330649,Human_RBP_ID_8226468,Human_RBP_ID_8944843,Human_RBP_ID_9443139,Human_RBP_ID_18963402 Human_Splice_Rec_2183045 82397 RMVar_ID_82397 Human_SNP_ID_708135746 m1A Human chrX - 2830032 2830032 2830032 AGGCCTGGGGGCGACAGCGTGGCAGTCTCGACACCCTCGGCTGCAGGCCCCGCCAGTGTCACCCC AGGCCTGGGGGCGACAGCGTGGCAGTCTCGACCCCCTCGGCTGCAGGCCCCGCCAGTGTCACCCC T G lnc-ARSD-6 RNACentral:URS0000D5C1C9 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2830028..2830129 26863196 MeRIP-seq:(Medium) rs936296653 Functional Loss SNV dbSNP153 33..33 33 - - - 82398 RMVar_ID_82398 Human_SNP_ID_708155945 m1A Human chrX - 2928949 2928949 2928949 AAGGGAAGGCGGAAGGGCAGGGAAAGAGAACAAAGGAGGAAGGGAAGGGAGGGCGGAGGAAGGCT AAGGGAAGGCGGAAGGGCAGGGAAAGAGAACACAGGAGGAAGGGAAGGGAGGGCGGAGGAAGGCT T G ARSD Ensembl:ENSG00000006756 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:2928945..2929031 26863196 MeRIP-seq:(Medium) rs1022143836 Functional Loss SNV dbSNP153 33..33 33 - - - 82399 RMVar_ID_82399 Human_SNP_ID_708273650 m1A Human chrX - 3524533 3524524 3524533 TGATGGTGGTGATGGTGGTGATGGTGATGGTGATGGTGGTGGTGATGGTGATGGTGGTGATGGTG TGATGGTGGTGATGGTGGTGATGGTGATGGTG_________GTGATGGTGATGGTGGTGATGGTG CCACCACCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3524496..3524561 26863196 MeRIP-seq:(Medium) rs1311283586 Functional Loss DEL dbSNP153 33..41 33 - - - 82400 RMVar_ID_82400 Human_SNP_ID_708273651 m1A Human chrX - 3524533 3524527 3524533 TGATGGTGGTGATGGTGGTGATGGTGATGGTGATGGTGGTGGTGATGGTGATGGTGGTGATGGTG TGATGGTGGTGATGGTGGTGATGGTGATGGTG______GTGGTGATGGTGATGGTGGTGATGGTG CCACCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3524496..3524561 26863196 MeRIP-seq:(Medium) rs773456450 Functional Loss DEL dbSNP153 33..38 33 - - - 82401 RMVar_ID_82401 Human_SNP_ID_708273658 m1A Human chrX - 3524533 3524533 3524533 TGATGGTGGTGATGGTGGTGATGGTGATGGTGATGGTGGTGGTGATGGTGATGGTGGTGATGGTG TGATGGTGGTGATGGTGGTGATGGTGATGGTGGTGGTGGTGGTGATGGTGATGGTGGTGATGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3524496..3524561 26863196 MeRIP-seq:(Medium) rs865985185 Functional Loss SNV dbSNP153 33..33 33 - - - 82402 RMVar_ID_82402 Human_SNP_ID_708273659 m1A Human chrX - 3524533 3524533 3524533 TGATGGTGGTGATGGTGGTGATGGTGATGGTGATGGTGGTGGTGATGGTGATGGTGGTGATGGTG TGATGGTGGTGATGGTGGTGATGGTGATGGTGCTGGTGGTGGTGATGGTGATGGTGGTGATGGTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3524496..3524561 26863196 MeRIP-seq:(Medium) rs865985185 Functional Loss SNV dbSNP153 33..33 33 - - - 82403 RMVar_ID_82403 Human_SNP_ID_708331125 m1A Human chrX + 3814802 3814802 3814802 TATGCGGCGGTCACGGGCCTCTCCGGCCCGGGAGACGGACGTTATGGCTGGCAGCGTCTCGATAC TATGCGGCGGTCACGGGCCTCTCCGGCCCGGGTGACGGACGTTATGGCTGGCAGCGTCTCGATAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3814752..3814862 26863196 MeRIP-seq:(Medium) rs1000996070 Functional Loss SNV dbSNP153 33..33 33 - - - 82404 RMVar_ID_82404 Human_SNP_ID_708335153 m1A Human chrX + 3838353 3838353 3838353 TAGAAAGAGTTCATGGCGGGGTGGCGGCGGGAAAAAAAAAAAAAAAGCTAACGCCGTGGCCGGTG TAGAAAGAGTTCATGGCGGGGTGGCGGCGGGAGAAAAAAAAAAAAAGCTAACGCCGTGGCCGGTG A G lnc-ARSF-6 RNACentral:URS00008BB39A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:3838311..3838509;chrX:3838297..3838380 26863196 MeRIP-seq:(Medium) rs1281687067 Functional Loss SNV dbSNP153 33..33 33 - - - 82405 RMVar_ID_82405 Human_SNP_ID_708335171 m1A Human chrX - 3838392 3838388 3838393 GTGGTGCTGATAACACCAAGGTCGCGGGCTCGACTCCCGCACCGGCCACGGCGTTAGCTTTTTTT GTGGTGCTGATAACACCAAGGTCGCGGGCTC_____CCGCACCGGCCACGGCGTTAGCTTTTTTT GGAGTC G BX890604.2 Ensembl:ENSG00000285756 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1247628037 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_76630,RMVar_hsa_circ_261244,RMVar_hsa_circ_261246,RMVar_hsa_circ_82160 82406 RMVar_ID_82406 Human_SNP_ID_708335176 m1A Human chrX - 3838392 3838392 3838392 GTGGTGCTGATAACACCAAGGTCGCGGGCTCGACTCCCGCACCGGCCACGGCGTTAGCTTTTTTT GTGGTGCTGATAACACCAAGGTCGCGGGCTCGGCTCCCGCACCGGCCACGGCGTTAGCTTTTTTT T C BX890604.2 Ensembl:ENSG00000285756 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1220674779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76630,RMVar_hsa_circ_261244,RMVar_hsa_circ_261246,RMVar_hsa_circ_82160 82407 RMVar_ID_82407 Human_SNP_ID_709240925 m1A Human chrX - 8732110 8732110 8732110 GGCTCAGTCGCGGCGTCTGCCTGGTCCTCAGCAGTGCAGCCCCGGCGCGGAGCAGGGAGCCTCGG GGCTCAGTCGCGGCGTCTGCCTGGTCCTCAGCGGTGCAGCCCCGGCGCGGAGCAGGGAGCCTCGG T C ANOS1 Ensembl:ENSG00000011201 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:8732061..8732132 26863196 MeRIP-seq:(Medium) rs1183612461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5085796 82408 RMVar_ID_82408 Human_SNP_ID_709377140 m1A Human chrX - 9465128 9465128 9465128 GCTGAGGCGGGCGCGGCGGCGGCGGCGGCGGCAGCGGGAGAGGGCGGGACAGCGGGAGGGACTGG GCTGAGGCGGGCGCGGCGGCGGCGGCGGCGGCGGCGGGAGAGGGCGGGACAGCGGGAGGGACTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chrX:9465062..9465238;chrX:9465079..9465232 26863196 MeRIP-seq:(Medium) rs902702582 Functional Loss SNV dbSNP153 33..33 33 - - - 82409 RMVar_ID_82409 Human_SNP_ID_709377213 m1A Human chrX - 9465376 9465351 9465376 CCGGCCGCGCTCCGAACCTCCCTCCAGCCGGCAGCCTCCGAGTCCCGGCCGTGCGGCGGCCGAAG CCGGCCGCGCTCCGAACCTCCCTCCAGCCGGC_________________________GGCCGAAG CGCCGCACGGCCGGGACTCGGAGGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:9465326..9465489 26863196 MeRIP-seq:(Medium) rs1464674024 Functional Loss DEL dbSNP153 33..57 33 - - - 82410 RMVar_ID_82410 Human_SNP_ID_709377240 m1A Human chrX - 9465483 9465483 9465483 CGCGGGACCCGCCTCCCCGCAGAAGTTTGCGGACCCCGCGCCCGGCCCGCCGAGCCCTGCGCACT CGCGGGACCCGCCTCCCCGCAGAAGTTTGCGGCCCCCGCGCCCGGCCCGCCGAGCCCTGCGCACT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:9465472..9465585 32194978 MeRIP-seq:(Medium) rs939099240 Functional Loss SNV dbSNP153 33..33 33 - - - 82411 RMVar_ID_82411 Human_SNP_ID_709390900 m1A Human chrX - 9533989 9533989 9533989 CATGGTTCTGGGTTCCTCCCTCGGAGCTCAGCACTGCCCAAGCACTGGGCACGGCAAGCCGGTGC CATGGTTCTGGGTTCCTCCCTCGGAGCTCAGCGCTGCCCAAGCACTGGGCACGGCAAGCCGGTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:9533988..9534080 26863196 MeRIP-seq:(Medium) rs1386284116 Functional Loss SNV dbSNP153 33..33 33 - - - 82412 RMVar_ID_82412 Human_SNP_ID_709394588 m1A Human chrX + 9553108 9553108 9553108 TAGGCTGTAGTGAGCCATGTTGGCGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACACTGTC TAGGCTGTAGTGAGCCATGTTGGCGCCACTGCTCTCCAGCCTGGGCAACAGAGCAAGACACTGTC A T TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:9553105..9553275 26863196 MeRIP-seq:(Medium) rs1346240316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9222 82413 RMVar_ID_82413 Human_SNP_ID_709404071 m1A Human chrX - 9601363 9601363 9601363 TGTATCTTTGCAATCTGTAGGACAAGAAAACCACCCATATGTACCTAGCCCAGGGAGTGTGTCCT TGTATCTTTGCAATCTGTAGGACAAGAAAACCGCCCATATGTACCTAGCCCAGGGAGTGTGTCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:9601361..9601461 26863196 MeRIP-seq:(Medium) rs1284648762 Functional Loss SNV dbSNP153 33..33 33 - - - 82414 RMVar_ID_82414 Human_SNP_ID_709419980 m1A Human chrX - 9688194 9688194 9688194 CTTCGATGGATTTTGGTGGGAAACGCCGGCTGAGGTCGTGGTGGCTGCTGTCGCTGCTGCCGTGG CTTCGATGGATTTTGGTGGGAAACGCCGGCTGGGGTCGTGGTGGCTGCTGTCGCTGCTGCCGTGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:9688075..9688250 26863196 MeRIP-seq:(Medium) rs762936211 Functional Loss SNV dbSNP153 33..33 33 - - - 82415 RMVar_ID_82415 Human_SNP_ID_709419990 m1A Human chrX + 9688220 9688220 9688220 ACGACCTCAGCCGGCGTTTCCCACCAAAATCCATCGAAGAACAGAGAGGCCACGGTGAATGGGGA ACGACCTCAGCCGGCGTTTCCCACCAAAATCCGTCGAAGAACAGAGAGGCCACGGTGAATGGGGA A G TBL1X Ensembl:ENSG00000101849 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:9688101..9688250 26863196 MeRIP-seq:(Medium) rs145895365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2184088,Human_Splice_Rec_2184120,Human_Splice_Rec_2184161,Human_Splice_Rec_2184203,Human_Splice_Rec_2184243,Human_Splice_Rec_2184277,Human_Splice_Rec_2184320 RMVar_hsa_circ_5640,RMVar_hsa_circ_17831,RMVar_hsa_circ_56869,RMVar_hsa_circ_35175,RMVar_hsa_circ_31556,RMVar_hsa_circ_91163,RMVar_hsa_circ_31040,RMVar_hsa_circ_26925,RMVar_hsa_circ_330212,RMVar_hsa_circ_261280,RMVar_hsa_circ_261281,RMVar_hsa_circ_371078,RMVar_hsa_circ_65295,RMVar_hsa_circ_302124,RMVar_hsa_circ_30439,RMVar_hsa_circ_10821,RMVar_hsa_circ_13487,RMVar_hsa_circ_261283,RMVar_hsa_circ_63110,RMVar_hsa_circ_357131,RMVar_hsa_circ_6657 82416 RMVar_ID_82416 Human_SNP_ID_709486182 m1A Human chrX + 10015314 10015311 10015314 GGGCGCGCCGCGGGAACGGAGGGGCGGCCGGCAGCGGCGGCGGCGGCGGCGGCGGCTCCCGGGCT GGGCGCGCCGCGGGAACGGAGGGGCGGCCG___GCGGCGGCGGCGGCGGCGGCGGCTCCCGGGCT GGCA G WWC3 Ensembl:ENSG00000047644 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:10015251..10015850;chrX:10015057..10015550;chrX:10015017..10015902;chrX:10015240..10015575 26863196 MeRIP-seq:(Medium) rs1224806482 Functional Loss DEL dbSNP153 31..33 33 - - - 82417 RMVar_ID_82417 Human_SNP_ID_709486184 m1A Human chrX + 10015314 10015314 10015314 GGGCGCGCCGCGGGAACGGAGGGGCGGCCGGCAGCGGCGGCGGCGGCGGCGGCGGCTCCCGGGCT GGGCGCGCCGCGGGAACGGAGGGGCGGCCGGCGGCGGCGGCGGCGGCGGCGGCGGCTCCCGGGCT A G WWC3 Ensembl:ENSG00000047644 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:10015251..10015850;chrX:10015057..10015550;chrX:10015017..10015902;chrX:10015240..10015575 26863196 MeRIP-seq:(Medium) rs766597204 Functional Loss SNV dbSNP153 33..33 33 - - - 82418 RMVar_ID_82418 Human_SNP_ID_709486269 m1A Human chrX + 10015617 10015617 10015617 TGGCTGAGCGGCGGCCGGCGGCGACGGCGGGGACAGCCGCGCGAGGCCCCGCGGGAGCCGCCGCC TGGCTGAGCGGCGGCCGGCGGCGACGGCGGGGGCAGCCGCGCGAGGCCCCGCGGGAGCCGCCGCC A G WWC3 Ensembl:ENSG00000047644 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:10015251..10015798 26863196 MeRIP-seq:(Medium) rs1464270189 Functional Loss SNV dbSNP153 33..33 33 - - - 82419 RMVar_ID_82419 Human_SNP_ID_709487556 m1A Human chrX + 10022656 10022656 10022656 ACTTTGCAGATGTGATTAAGTTAAGGATCTTGAGATAAGGAGATGATCCTGGATTATGTGGGTGG ACTTTGCAGATGTGATTAAGTTAAGGATCTTGGGATAAGGAGATGATCCTGGATTATGTGGGTGG A G WWC3 Ensembl:ENSG00000047644 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:10022653..10022808 26863196 MeRIP-seq:(Medium) rs1371486872 Functional Loss SNV dbSNP153 33..33 33 - - - 82420 RMVar_ID_82420 Human_SNP_ID_709489194 m1A Human chrX - 10032132 10032132 10032132 CTCTCCAGCCGCTCTCCACAAAACGGTCACCCACCCAGCCACACAGTCCCACCAACCTCACCCTG CTCTCCAGCCGCTCTCCACAAAACGGTCACCCCCCCAGCCACACAGTCCCACCAACCTCACCCTG T G WWC3-AS1 Ensembl:ENSG00000225076 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:10032128..10032272 26863196 MeRIP-seq:(Medium) rs948613083 Functional Loss SNV dbSNP153 33..33 33 - - - 82421 RMVar_ID_82421 Human_SNP_ID_709502410 m1A Human chrX + 10109915 10109915 10109915 CCTGCTGCAGGAGCTTCAGCTCATCATTGCACAGCGCCGCTCTGCGGGAGATGTGGCCCGGCTGG CCTGCTGCAGGAGCTTCAGCTCATCATTGCACGGCGCCGCTCTGCGGGAGATGTGGCCCGGCTGG A G WWC3 Ensembl:ENSG00000047644 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:10109870..10110058 26863196 MeRIP-seq:(Medium) rs767758080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1523,RMVar_hsa_circ_279092,RMVar_hsa_circ_271151,RMVar_hsa_circ_75921,RMVar_hsa_circ_38087,RMVar_hsa_circ_261301,RMVar_hsa_circ_261302,RMVar_hsa_circ_261303,RMVar_hsa_circ_265728,RMVar_hsa_circ_14113,RMVar_hsa_circ_329404,RMVar_hsa_circ_286198,RMVar_hsa_circ_297052,RMVar_hsa_circ_338434,RMVar_hsa_circ_266079,RMVar_hsa_circ_261306,RMVar_hsa_circ_261307,RMVar_hsa_circ_82678,RMVar_hsa_circ_99942,RMVar_hsa_circ_261311,RMVar_hsa_circ_20376,RMVar_hsa_circ_261310 82422 RMVar_ID_82422 Human_SNP_ID_709566204 m1A Human chrX - 10467626 10467626 10467626 TCAGAGGTATAACTAGAAGGTGACTCAGGAGCACTGTGGAGAGTGGAGAGGAACAGGGCAGGACC TCAGAGGTATAACTAGAAGGTGACTCAGGAGCTCTGTGGAGAGTGGAGAGGAACAGGGCAGGACC T A MID1 Ensembl:ENSG00000101871 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:10467576..10467739 26863196 MeRIP-seq:(Medium) rs1206411446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7963178,Human_RBP_ID_10444917,Human_RBP_ID_16782310 RMVar_hsa_circ_1696,RMVar_hsa_circ_353430 82423 RMVar_ID_82423 Human_SNP_ID_709586099 m1A Human chrX - 10588610 10588610 10588610 AGTCAGAGAGAGACAGAGAGACAGAAAGTCAAAGAGAGAAAGAAAAAGAGAAAGAGAGAAATATA AGTCAGAGAGAGACAGAGAGACAGAAAGTCAATGAGAGAAAGAAAAAGAGAAAGAGAGAAATATA T A MID1 Ensembl:ENSG00000101871 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:10588608..10588687 26863196 MeRIP-seq:(Medium) rs1030333594 Functional Loss SNV dbSNP153 33..33 33 - - - 82424 RMVar_ID_82424 Human_SNP_ID_709673083 m1A Human chrX - 11112004 11112004 11112004 ACAATTTTAAATTTCCACCTGCCAAAACAAAGAGACAGATTAATGTCTCTGGACTCAGACTATTC ACAATTTTAAATTTCCACCTGCCAAAACAAAGGGACAGATTAATGTCTCTGGACTCAGACTATTC T C lnc-ARHGAP6-3 RNACentral:URS00008B5AB0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:11112001..11112100 26863196 MeRIP-seq:(Medium) rs924100440 Functional Loss SNV dbSNP153 33..33 33 - - - 82425 RMVar_ID_82425 Human_SNP_ID_709673633 m1A Human chrX - 11114953 11114953 11114953 AGATTTGAAGGATCTAGGTTCTCCTTATTCTCAGCCGCAGTGCCCCTAATGGGACACTCCACGTA AGATTTGAAGGATCTAGGTTCTCCTTATTCTCCGCCGCAGTGCCCCTAATGGGACACTCCACGTA T G lnc-ARHGAP6-3 RNACentral:URS00008B5AB0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:11114902..11115031 26863196 MeRIP-seq:(Medium) rs1467650525 Functional Loss SNV dbSNP153 33..33 33 - - - 82426 RMVar_ID_82426 Human_SNP_ID_709962501 m1A Human chrX + 12791420 12791420 12791420 TAGCCGCCGCGCTTTCCCGCTCCCGCAGCAGCAGCCTCCCGCGTCGCTGTCGCTGTTGCCTCCGC TAGCCGCCGCGCTTTCCCGCTCCCGCAGCAGCCGCCTCCCGCGTCGCTGTCGCTGTTGCCTCCGC A C PRPS2 Ensembl:ENSG00000101911 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:12791376..12791565 26863196 MeRIP-seq:(Medium) rs1282107207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727573,Human_RBP_ID_5076012,Human_RBP_ID_9339876 RMVar_hsa_circ_101679,RMVar_hsa_circ_261342 82427 RMVar_ID_82427 Human_SNP_ID_709962509 m1A Human chrX - 12791443 12791438 12791444 GGCGCGCGGCGGCGGAGGAGGTGGCGGAGGCAACAGCGACAGCGACGCGGGAGGCTGCTGCTGCG GGCGCGCGGCGGCGGAGGAGGTGGCGGAGGC______GACAGCGACGCGGGAGGCTGCTGCTGCG CGCTGTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:12791376..12791669 26863196 MeRIP-seq:(Medium) rs1385756156 Functional Loss DEL dbSNP153 32..37 33 - - - 82428 RMVar_ID_82428 Human_SNP_ID_709962509 m1A Human chrX - 12791444 12791438 12791444 GGGCGCGCGGCGGCGGAGGAGGTGGCGGAGGCAACAGCGACAGCGACGCGGGAGGCTGCTGCTGC GGGCGCGCGGCGGCGGAGGAGGTGGCGGAGGC______GACAGCGACGCGGGAGGCTGCTGCTGC CGCTGTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:12791376..12791625 26863196 MeRIP-seq:(Medium) rs1385756156 Functional Loss DEL dbSNP153 33..38 33 - - - 82429 RMVar_ID_82429 Human_SNP_ID_709962513 m1A Human chrX - 12791448 12791448 12791448 CGAGGGGCGCGCGGCGGCGGAGGAGGTGGCGGAGGCAACAGCGACAGCGACGCGGGAGGCTGCTG CGAGGGGCGCGCGGCGGCGGAGGAGGTGGCGGTGGCAACAGCGACAGCGACGCGGGAGGCTGCTG T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:12791402..12791522 26863196 MeRIP-seq:(Medium) rs761998122 Functional Loss SNV dbSNP153 33..33 33 - - - 82430 RMVar_ID_82430 Human_SNP_ID_709963776 m1A Human chrX + 12799164 12799164 12799164 CCTAGGGGTGGTCTCAGGGACGCCCAAGATGCAAATATGCTTCGATATTAACCGATGGCAGTTTT CCTAGGGGTGGTCTCAGGGACGCCCAAGATGCGAATATGCTTCGATATTAACCGATGGCAGTTTT A G PRPS2 Ensembl:ENSG00000101911 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:12799160..12799334 26863196 MeRIP-seq:(Medium) rs761148164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101679,RMVar_hsa_circ_261342 82431 RMVar_ID_82431 Human_SNP_ID_709997187 m1A Human chrX - 12975976 12975976 12975976 CAAAGCCGAATCTTGCAGAATAAAGGAAATTGACCACTGCGAATTGTTAATTACAGCGTTTAAAA CAAAGCCGAATCTTGCAGAATAAAGGAAATTGGCCACTGCGAATTGTTAATTACAGCGTTTAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:12975974..12976275 26863196 MeRIP-seq:(Medium) rs1156973285 Functional Loss SNV dbSNP153 33..33 33 - - - 82432 RMVar_ID_82432 Human_SNP_ID_709997251 m1A Human chrX - 12976228 12976228 12976228 GTTGCGGAGGAAAAGCTGCAGGGAGCAAGCCAAGAGCGAGCGTGAGGAAGAGCCACCCGCCCCGC GTTGCGGAGGAAAAGCTGCAGGGAGCAAGCCAGGAGCGAGCGTGAGGAAGAGCCACCCGCCCCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:12976226..12976300 26863196 MeRIP-seq:(Medium) rs1458727398 Functional Loss SNV dbSNP153 33..33 33 - - - 82433 RMVar_ID_82433 Human_SNP_ID_709997252 m1A Human chrX - 12976229 12976229 12976229 GGTTGCGGAGGAAAAGCTGCAGGGAGCAAGCCAAGAGCGAGCGTGAGGAAGAGCCACCCGCCCCG GGTTGCGGAGGAAAAGCTGCAGGGAGCAAGCCGAGAGCGAGCGTGAGGAAGAGCCACCCGCCCCG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:12976226..12976300 26863196 MeRIP-seq:(Medium) rs1452366737 Functional Loss SNV dbSNP153 33..33 33 - - - 82434 RMVar_ID_82434 Human_SNP_ID_709997478 m1A Human chrX + 12976999 12976999 12976999 AGGCCGCGCCTGCCTTTCCCATCTGTCTATCTATCTGGCTGGCAGGGAAGGAAAGAACTTGCATG AGGCCGCGCCTGCCTTTCCCATCTGTCTATCTGTCTGGCTGGCAGGGAAGGAAAGAACTTGCATG A G TMSB4X Ensembl:ENSG00000205542 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:12976971..12977091 26863196 MeRIP-seq:(Medium) rs762846337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94567,Human_RBP_ID_728074,Human_RBP_ID_1120374,Human_RBP_ID_5637409,Human_RBP_ID_7976155,Human_RBP_ID_17442666,Human_RBP_ID_17717664,Human_RBP_ID_18213351,Human_RBP_ID_24328872,Human_RBP_ID_24525770,Human_RBP_ID_26834575,Human_RBP_ID_27549725 Human_miRNA_ID_2398779 RMVar_hsa_circ_100600,RMVar_hsa_circ_261357,RMVar_hsa_circ_124817,RMVar_hsa_circ_261353,RMVar_hsa_circ_377009,RMVar_hsa_circ_261356,RMVar_hsa_circ_378535,RMVar_hsa_circ_261358 82435 RMVar_ID_82435 Human_SNP_ID_709997516 m1A Human chrX - 12977151 12977151 12977151 TCCAATAATTAAAATCATTTGAACAAAAAAAAAAATGGCACTCTGATTAAACTGCATTACAGCCT TCCAATAATTAAAATCATTTGAACAAAAAAAAGAATGGCACTCTGATTAAACTGCATTACAGCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:12977126..12977150 26863196 MeRIP-seq:(Medium) rs1265741977 Functional Loss SNV dbSNP153 33..33 33 - - - 82436 RMVar_ID_82436 Human_SNP_ID_710063085 m1A Human chrX - 13379047 13379047 13379047 GAAGAGATTCTGAATTCCCTCAAGTACGTCCGACCTGGTGGTGGGTTCGAGCCCAACTTCATGCT GAAGAGATTCTGAATTCCCTCAAGTACGTCCGGCCTGGTGGTGGGTTCGAGCCCAACTTCATGCT T C GPX1P1 Ensembl:ENSG00000197582 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879163336 Functional Loss SNV dbSNP153 33..33 33 - - - 82437 RMVar_ID_82437 Human_SNP_ID_710063156 m1A Human chrX - 13379306 13379306 13379306 GTGTGCTGCTCGGCCAGCGGCGGCGGCGGCCCAGTCGGTGTATGCCTTCTCGGCGCGCCCGCTGG GTGTGCTGCTCGGCCAGCGGCGGCGGCGGCCCCGTCGGTGTATGCCTTCTCGGCGCGCCCGCTGG T G GPX1P1 Ensembl:ENSG00000197582 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:13379265..13379375;chrX:13379207..13379350;chrX:13379203..13379350;chrX:13379276..13379375;chrX:13379276..13379350 26863196 MeRIP-seq:(Medium) rs1232068620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076477,Human_RBP_ID_5232485,Human_RBP_ID_17674220,Human_RBP_ID_18927577,Human_RBP_ID_21960905,Human_RBP_ID_27144021 Human_miRNA_ID_1897855 82438 RMVar_ID_82438 Human_SNP_ID_710117917 m1A Human chrX - 13689201 13689201 13689201 ATGAGGACAGAGAGAGGGTCGGGGACCTGCACAGCAGGAGGCAGCCGCGGTAGCGCAGCCAGGCT ATGAGGACAGAGAGAGGGTCGGGGACCTGCACTGCAGGAGGCAGCCGCGGTAGCGCAGCCAGGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:13689151..13689342 26863196 MeRIP-seq:(Medium) rs1291358494 Functional Loss SNV dbSNP153 33..33 33 - - - 82439 RMVar_ID_82439 Human_SNP_ID_710117947 m1A Human chrX - 13689272 13689272 13689272 CCCGAGTCCCGCTCACCTCGCGGCCACACGAAAGACGACCCGGGAGCTCTGGGCCGGCCCGTCTG CCCGAGTCCCGCTCACCTCGCGGCCACACGAAGGACGACCCGGGAGCTCTGGGCCGGCCCGTCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:13689222..13703768 32194978 MeRIP-seq:(Medium) rs772375520 Functional Loss SNV dbSNP153 33..33 33 - - - 82440 RMVar_ID_82440 Human_SNP_ID_710118872 m1A Human chrX - 13693348 13693348 13693348 CATTTTTTGAGTTCACCCTCACTCCTCTACAAAAAAGTCCTTAATAAATGTTCTCTGTTGATGGC CATTTTTTGAGTTCACCCTCACTCCTCTACAAGAAAGTCCTTAATAAATGTTCTCTGTTGATGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:13693346..13693542 26863196 MeRIP-seq:(Medium) rs1228491771 Functional Loss SNV dbSNP153 33..33 33 - - - 82441 RMVar_ID_82441 Human_SNP_ID_710126072 m1A Human chrX - 13733325 13733325 13733325 AGTAAACGAGTCAACGCTAGCAGAGGTGGAACAATAGGGCTGAGAAAAGACACGTGGAGCAATGT AGTAAACGAGTCAACGCTAGCAGAGGTGGAACGATAGGGCTGAGAAAAGACACGTGGAGCAATGT T C TRAPPC2 Ensembl:ENSG00000196459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:13733323..13733509 26863196 MeRIP-seq:(Medium) rs904581812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16833564 82442 RMVar_ID_82442 Human_SNP_ID_710126080 m1A Human chrX - 13733361 13733359 13733361 CTCGATATAGTCAAAGTGAATTTGGGAGAAAAAATAAGTAAACGAGTCAACGCTAGCAGAGGTGG CTCGATATAGTCAAAGTGAATTTGGGAGAAAA__TAAGTAAACGAGTCAACGCTAGCAGAGGTGG ATT A TRAPPC2 Ensembl:ENSG00000196459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:13733359..13733506 26863196 MeRIP-seq:(Medium) rs1213035837 Functional Loss DEL dbSNP153 33..34 33 - - - 82443 RMVar_ID_82443 Human_SNP_ID_710136775 m1A Human chrX - 13785791 13785791 13785791 CTCCTTTGGGTTCAGGCTGCTTTGAATGCTGCATCAAGTGTCTGGGAGGAGTCCCCTACGCCTCC CTCCTTTGGGTTCAGGCTGCTTTGAATGCTGCGTCAAGTGTCTGGGAGGAGTCCCCTACGCCTCC T C GPM6B Ensembl:ENSG00000046653 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:13785740..13785844 26863196 MeRIP-seq:(Medium) rs372150817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9244052 Human_Splice_Rec_2186910,Human_Splice_Rec_2186922,Human_Splice_Rec_2186938,Human_Splice_Rec_2186960,Human_Splice_Rec_2186972,Human_Splice_Rec_2186984,Human_Splice_Rec_2187004,Human_Splice_Rec_2187010,Human_Splice_Rec_2187018 Human_miRNA_ID_1938729,Human_miRNA_ID_1949829 RMVar_hsa_circ_261378,RMVar_hsa_circ_370786,RMVar_hsa_circ_25716,RMVar_hsa_circ_301082,RMVar_hsa_circ_261380,RMVar_hsa_circ_261381 82444 RMVar_ID_82444 Human_SNP_ID_710327027 m1A Human chrX + 14873507 14873507 14873507 GCGACGGTAGAACGGGCGACGGCGACAACCGCAATCACATCCACGACGGTGATCATGGCAGAGGT GCGACGGTAGAACGGGCGACGGCGACAACCGCCATCACATCCACGACGGTGATCATGGCAGAGGT A C MOSPD2 Ensembl:ENSG00000130150 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:14873466..14873741 26863196 MeRIP-seq:(Medium) rs1008223099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257989 Human_Splice_Rec_2187221,Human_Splice_Rec_2187249,Human_Splice_Rec_2187277,Human_Splice_Rec_2187281 82445 RMVar_ID_82445 Human_SNP_ID_710327029 m1A Human chrX - 14873509 14873509 14873509 TCACCTCTGCCATGATCACCGTCGTGGATGTGATTGCGGTTGTCGCCGTCGCCCGTTCTACCGTC TCACCTCTGCCATGATCACCGTCGTGGATGTGTTTGCGGTTGTCGCCGTCGCCCGTTCTACCGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:14873458..14873741 26863196 MeRIP-seq:(Medium) rs1242297077 Functional Loss SNV dbSNP153 33..33 33 - - - 82446 RMVar_ID_82446 Human_SNP_ID_162450342 m1A Human chr3 - 168027780 168027780 168027780 AGATGAAGCAGAAGGAGATCCAGGTAATAGACATGAGCCTCGTGAACAAGGACCCCGAGAAGCCG AGATGAAGCAGAAGGAGATCCAGGTAATAGACTTGAGCCTCGTGAACAAGGACCCCGAGAAGCCG T A GOLIM4 Ensembl:ENSG00000173905 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:168027668..168027861 26863196 MeRIP-seq:(Medium) rs372302207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69046,Human_RBP_ID_939393,Human_RBP_ID_14709958,Human_RBP_ID_24383953,Human_RBP_ID_26347353,Human_RBP_ID_27822652 Human_Splice_Rec_504856,Human_Splice_Rec_504857,Human_Splice_Rec_504884,Human_Splice_Rec_504885 RMVar_hsa_circ_66119,RMVar_hsa_circ_114495,RMVar_hsa_circ_268973,RMVar_hsa_circ_222509,RMVar_hsa_circ_350185,RMVar_hsa_circ_41864,RMVar_hsa_circ_60242,RMVar_hsa_circ_222510,RMVar_hsa_circ_361955 82447 RMVar_ID_82447 Human_SNP_ID_162450343 m1A Human chr3 - 168027780 168027780 168027780 AGATGAAGCAGAAGGAGATCCAGGTAATAGACATGAGCCTCGTGAACAAGGACCCCGAGAAGCCG AGATGAAGCAGAAGGAGATCCAGGTAATAGACGTGAGCCTCGTGAACAAGGACCCCGAGAAGCCG T C GOLIM4 Ensembl:ENSG00000173905 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:168027668..168027861 26863196 MeRIP-seq:(Medium) rs372302207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69046,Human_RBP_ID_939393,Human_RBP_ID_14709958,Human_RBP_ID_24383953,Human_RBP_ID_26347353,Human_RBP_ID_27822652 Human_Splice_Rec_504856,Human_Splice_Rec_504857,Human_Splice_Rec_504884,Human_Splice_Rec_504885 RMVar_hsa_circ_66119,RMVar_hsa_circ_114495,RMVar_hsa_circ_268973,RMVar_hsa_circ_222509,RMVar_hsa_circ_350185,RMVar_hsa_circ_41864,RMVar_hsa_circ_60242,RMVar_hsa_circ_222510,RMVar_hsa_circ_361955 82448 RMVar_ID_82448 Human_SNP_ID_162467084 m1A Human chr3 - 168095574 168095574 168095574 GGCAGGAGGCATCTGGGGACAGGCGCGAGGGCAGCCGGCTCTGAAGTATGCGGAGGGCCTCCTCC GGCAGGAGGCATCTGGGGACAGGCGCGAGGGCTGCCGGCTCTGAAGTATGCGGAGGGCCTCCTCC T A GOLIM4 Ensembl:ENSG00000173905 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:168095229..168095886;chr3:168095260..168095889;chr3:168095249..168095902 26863196 MeRIP-seq:(Medium) rs11065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756822,Human_RBP_ID_5530712,Human_RBP_ID_22456332,Human_RBP_ID_26347360 82449 RMVar_ID_82449 Human_SNP_ID_162467110 m1A Human chr3 + 168095673 168095673 168095673 CCCCGGGCAGTTCTTGGAGTCCCGCCCTGGCCACTCCCCGCCCTATCGCGGCGGCTCCCACTGCA CCCCGGGCAGTTCTTGGAGTCCCGCCCTGGCCGCTCCCCGCCCTATCGCGGCGGCTCCCACTGCA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:168095579..168095847 26863196 MeRIP-seq:(Medium) rs958569821 Functional Loss SNV dbSNP153 33..33 33 - - - 82450 RMVar_ID_82450 Human_SNP_ID_162842780 m1A Human chr3 + 169663390 169663390 169663390 GCCTTTGGATCTCATGCTGTGCCCAGTCCTGCAGCCGCTGGTGTGTGGTTGGGGCTTTTTTTTCT GCCTTTGGATCTCATGCTGTGCCCAGTCCTGCCGCCGCTGGTGTGTGGTTGGGGCTTTTTTTTCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:169663340..169663619 26863196 MeRIP-seq:(Medium) rs1156547857 Functional Loss SNV dbSNP153 33..33 33 - - - 82451 RMVar_ID_82451 Human_SNP_ID_162842781 m1A Human chr3 + 169663390 169663390 169663390 GCCTTTGGATCTCATGCTGTGCCCAGTCCTGCAGCCGCTGGTGTGTGGTTGGGGCTTTTTTTTCT GCCTTTGGATCTCATGCTGTGCCCAGTCCTGCTGCCGCTGGTGTGTGGTTGGGGCTTTTTTTTCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:169663340..169663619 26863196 MeRIP-seq:(Medium) rs1156547857 Functional Loss SNV dbSNP153 33..33 33 - - - 82452 RMVar_ID_82452 Human_SNP_ID_162867266 m1A Human chr3 + 169764734 169764734 169764734 AAAGGCCTGAACCTCGCCCTCGCCCCCGAGAGACCCGCGGCTGACAGAGCCCAACTCTTCGCGGT AAAGGCCTGAACCTCGCCCTCGCCCCCGAGAGTCCCGCGGCTGACAGAGCCCAACTCTTCGCGGT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:169764658..169764756 26863410 MeRIP-seq:(Medium) rs1337845154 Functional Loss SNV dbSNP153 33..33 33 - - - 82453 RMVar_ID_82453 Human_SNP_ID_162867333 m1A Human chr3 - 169764892 169764892 169764892 CCTGCCGCCTTCCACCGTTCATTCTAGAGCAAACAAAAAATGTCAGCTGCTGGCCCGTTCGCCCC CCTGCCGCCTTCCACCGTTCATTCTAGAGCAAGCAAAAAATGTCAGCTGCTGGCCCGTTCGCCCC T C TERC,AC078802.2 Ensembl:ENSG00000270141,Ensembl:ENSG00000277925 lincRNA,Other exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:169764681..169765050 26863196 MeRIP-seq:(Medium) rs1439415851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064078,Human_RBP_ID_2807043,Human_RBP_ID_5250218,Human_RBP_ID_7240596,Human_RBP_ID_8564831,Human_RBP_ID_8869370,Human_RBP_ID_14717018,Human_RBP_ID_20969357,Human_RBP_ID_22533880,Human_RBP_ID_25768119,Human_RBP_ID_27048870 82454 RMVar_ID_82454 Human_SNP_ID_162867382 m1A Human chr3 - 169764999 169764999 169764999 GGTGGCCATTTTTTGTCTAACCCTAACTGAGAAGGGCGTAGGCGCCGTGCTTTTGCTCCCCGCGC GGTGGCCATTTTTTGTCTAACCCTAACTGAGATGGGCGTAGGCGCCGTGCTTTTGCTCCCCGCGC T A TERC,AC078802.2 Ensembl:ENSG00000270141,Ensembl:ENSG00000277925 lincRNA,Other exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:169764976..169765000 26863196 MeRIP-seq:(Medium) rs1203113072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936478,Human_RBP_ID_1064078,Human_RBP_ID_2764881,Human_RBP_ID_4759037,Human_RBP_ID_5209612,Human_RBP_ID_5299059,Human_RBP_ID_5605092,Human_RBP_ID_7154121,Human_RBP_ID_8869371,Human_RBP_ID_14717028,Human_RBP_ID_18169354,Human_RBP_ID_18464493,Human_RBP_ID_20969360,Human_RBP_ID_22551861,Human_RBP_ID_22676814,Human_RBP_ID_22745099,Human_RBP_ID_25768120 Human_miRNA_ID_3148108,Human_miRNA_ID_3211112 82455 RMVar_ID_82455 Human_SNP_ID_162867383 m1A Human chr3 - 169764999 169764999 169764999 GGTGGCCATTTTTTGTCTAACCCTAACTGAGAAGGGCGTAGGCGCCGTGCTTTTGCTCCCCGCGC GGTGGCCATTTTTTGTCTAACCCTAACTGAGAGGGGCGTAGGCGCCGTGCTTTTGCTCCCCGCGC T C TERC,AC078802.2 Ensembl:ENSG00000270141,Ensembl:ENSG00000277925 lincRNA,Other exon,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:169764976..169765000 26863196 MeRIP-seq:(Medium) rs1203113072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936478,Human_RBP_ID_1064078,Human_RBP_ID_2764881,Human_RBP_ID_4759037,Human_RBP_ID_5209612,Human_RBP_ID_5299059,Human_RBP_ID_5605092,Human_RBP_ID_7154121,Human_RBP_ID_8869371,Human_RBP_ID_14717028,Human_RBP_ID_18169354,Human_RBP_ID_18464493,Human_RBP_ID_20969360,Human_RBP_ID_22551861,Human_RBP_ID_22676814,Human_RBP_ID_22745099,Human_RBP_ID_25768120 Human_miRNA_ID_3148108,Human_miRNA_ID_3211112 82456 RMVar_ID_82456 Human_SNP_ID_162868908 m1A Human chr3 + 169769709 169769709 169769709 CGGAAGGACTCGCTGGACGCACCGTGCTCCTCATGTTACCGCCCGCTATTGCTTCTCGCAGGAAT CGGAAGGACTCGCTGGACGCACCGTGCTCCTCCTGTTACCGCCCGCTATTGCTTCTCGCAGGAAT A C AC078802.1 Ensembl:ENSG00000269889 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:169769659..169769768 26863196 MeRIP-seq:(Medium) rs1337824427 Functional Loss SNV dbSNP153 33..33 33 - - - 82457 RMVar_ID_82457 Human_SNP_ID_162917307 m1A Human chr3 + 169966853 169966853 169966853 ACATGGCGGAACGCAGGAGACACAAGAAGCGGATCCAGGTAGCAAAGCCGAGCTCTGGGCAGGGG ACATGGCGGAACGCAGGAGACACAAGAAGCGGGTCCAGGTAGCAAAGCCGAGCTCTGGGCAGGGG A G SEC62 Ensembl:ENSG00000008952 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:169966801..169966933;chr3:169966801..169966934 26863196 MeRIP-seq:(Medium) rs1461540335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248072,Human_RBP_ID_785012,Human_RBP_ID_834846,Human_RBP_ID_19011024,Human_RBP_ID_19116252,Human_RBP_ID_23026556,Human_RBP_ID_24547333 Human_Splice_Rec_505669,Human_Splice_Rec_505671,Human_Splice_Rec_505679,Human_Splice_Rec_505693,Human_Splice_Rec_505709,Human_Splice_Rec_505717,Human_Splice_Rec_505729 82458 RMVar_ID_82458 Human_SNP_ID_162917308 m1A Human chr3 - 169966854 169966854 169966854 CCCCCTGCCCAGAGCTCGGCTTTGCTACCTGGATCCGCTTCTTGTGTCTCCTGCGTTCCGCCATG CCCCCTGCCCAGAGCTCGGCTTTGCTACCTGGCTCCGCTTCTTGTGTCTCCTGCGTTCCGCCATG T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:169966836..169966913;chr3:169966801..169966933 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 82459 RMVar_ID_82459 Human_SNP_ID_162919327 m1A Human chr3 + 169975610 169975610 169975610 TTATACTAAATTAATATTCATATGTTGCAGGAAGTTGGTGAACCATCTAAAGAAGAGAAGGCTGT TTATACTAAATTAATATTCATATGTTGCAGGAGGTTGGTGAACCATCTAAAGAAGAGAAGGCTGT A G SEC62 Ensembl:ENSG00000008952 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:169975601..169982702 26863196 MeRIP-seq:(Medium) rs914053455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_594595,Human_RBP_ID_834406,Human_RBP_ID_938257,Human_RBP_ID_1622132,Human_RBP_ID_1955369,Human_RBP_ID_4757549,Human_RBP_ID_9394236,Human_RBP_ID_14717794,Human_RBP_ID_22678210,Human_RBP_ID_24547334,Human_RBP_ID_26347361,Human_RBP_ID_27822658 Human_Splice_Rec_505672,Human_Splice_Rec_505680,Human_Splice_Rec_505694,Human_Splice_Rec_505712,Human_Splice_Rec_505718,Human_Splice_Rec_505730 RMVar_hsa_circ_222544,RMVar_hsa_circ_59141,RMVar_hsa_circ_282595,RMVar_hsa_circ_338152,RMVar_hsa_circ_364024,RMVar_hsa_circ_309214,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546 82460 RMVar_ID_82460 Human_SNP_ID_162933637 m1A Human chr3 - 170038147 170038147 170038147 GCCCCGACACCTGCAGCGCCCGTGCCCAGGTGACCGCCCGAGGGAGGGGCGAGGGCCCAGCTCGC GCCCCGACACCTGCAGCGCCCGTGCCCAGGTGCCCGCCCGAGGGAGGGGCGAGGGCCCAGCTCGC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170038044..170038235 26863196 MeRIP-seq:(Medium) rs1223554801 Functional Loss SNV dbSNP153 33..33 33 - - - 82461 RMVar_ID_82461 Human_SNP_ID_162933643 m1A Human chr3 + 170038157 170038157 170038157 CCCTCGCCCCTCCCTCGGGCGGTCACCTGGGCACGGGCGCTGCAGGTGTCGGGGCCTCAACCTTG CCCTCGCCCCTCCCTCGGGCGGTCACCTGGGCGCGGGCGCTGCAGGTGTCGGGGCCTCAACCTTG A G GPR160 Ensembl:ENSG00000173890 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:170038064..170038193 26863196 MeRIP-seq:(Medium) rs1413195019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756827,Human_RBP_ID_9333938,Human_RBP_ID_9354345 Human_Splice_Rec_505753,Human_Splice_Rec_505759,Human_Splice_Rec_505767 82462 RMVar_ID_82462 Human_SNP_ID_162933650 m1A Human chr3 - 170038173 170038173 170038173 ATGGCTGTCGGCTCCGCAAGGTTGAGGCCCCGACACCTGCAGCGCCCGTGCCCAGGTGACCGCCC ATGGCTGTCGGCTCCGCAAGGTTGAGGCCCCGCCACCTGCAGCGCCCGTGCCCAGGTGACCGCCC T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:170038077..170038177 26863410 MeRIP-seq:(Medium) rs1559978435 Functional Loss SNV dbSNP153 33..33 33 - - - 82463 RMVar_ID_82463 Human_SNP_ID_162964125 m1A Human chr3 + 170162846 170162846 170162846 ATCTTTAAACCACACTCCCACTCTCACATTCCACTCCAGCCACACTGTCCTCCTTTCTGTTCCCT ATCTTTAAACCACACTCCCACTCTCACATTCCCCTCCAGCCACACTGTCCTCCTTTCTGTTCCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170162759..170162992 26863196 MeRIP-seq:(Medium) rs1022931450 Functional Loss SNV dbSNP153 33..33 33 - - - 82464 RMVar_ID_82464 Human_SNP_ID_162968497 m1A Human chr3 - 170178878 170178878 170178878 ACTGAACCAAACCCGGGAACATCTTCTGTGTCAACAACAACCAGCAGTACCACCACCACCACCAT ACTGAACCAAACCCGGGAACATCTTCTGTGTCGACAACAACCAGCAGTACCACCACCACCACCAT T C PHC3 Ensembl:ENSG00000173889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:170178829..170178894 26863196 MeRIP-seq:(Medium) rs1237242261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69042,Human_RBP_ID_9394244,Human_RBP_ID_14720513,Human_RBP_ID_17292839,Human_RBP_ID_17518332,Human_RBP_ID_18424081,Human_RBP_ID_26347374 Human_Splice_Rec_505802,Human_Splice_Rec_505830,Human_Splice_Rec_505858,Human_Splice_Rec_505888,Human_Splice_Rec_505898,Human_Splice_Rec_505910,Human_Splice_Rec_505918,Human_Splice_Rec_505930,Human_Splice_Rec_505938,Human_Splice_Rec_505948,Human_Splice_Rec_505956,Human_Splice_Rec_505962,Human_Splice_Rec_505968 Human_miRNA_ID_2782208,Human_miRNA_ID_2785176 RMVar_hsa_circ_369993,RMVar_hsa_circ_222560,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_222592,RMVar_hsa_circ_222590,RMVar_hsa_circ_94971,RMVar_hsa_circ_270479,RMVar_hsa_circ_77849,RMVar_hsa_circ_222593,RMVar_hsa_circ_116931,RMVar_hsa_circ_283172,RMVar_hsa_circ_86769,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_303083,RMVar_hsa_circ_222609,RMVar_hsa_circ_271991,RMVar_hsa_circ_340885,RMVar_hsa_circ_222611 82465 RMVar_ID_82465 Human_SNP_ID_162980069 m1A Human chr3 + 170222566 170222566 170222566 GCTGCGGGCGAGGTGGGCAGGTAGGTGGGCGGACGGCCGCGGTTCTCCGGCAAGCGCAGGCGGCG GCTGCGGGCGAGGTGGGCAGGTAGGTGGGCGGGCGGCCGCGGTTCTCCGGCAAGCGCAGGCGGCG A G PRKCI Ensembl:ENSG00000163558 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:170222401..170222775;chr3:170222417..170235273 26863196 MeRIP-seq:(Medium) rs1386689824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4730734,Human_RBP_ID_5473963,Human_RBP_ID_9302545,Human_RBP_ID_18424503,Human_RBP_ID_27841486 82466 RMVar_ID_82466 Human_SNP_ID_162983370 m1A Human chr3 + 170235181 170235181 170235181 CAAATTGTCAAGCATTCAGTAATATATACAGCATTATTATTTTTAATCATTTTCAAACTGAAAAC CAAATTGTCAAGCATTCAGTAATATATACAGCGTTATTATTTTTAATCATTTTCAAACTGAAAAC A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:170235177..170235313 26863196 MeRIP-seq:(Medium) rs370076127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7155321 82467 RMVar_ID_82467 Human_SNP_ID_163014352 m1A Human chr3 + 170357386 170357386 170357386 GGGCCAGAAGCGCCGGGCGCGCGCCTGGGGGGAGGGGCACGCGCGCGAGACGACGGGGCCAGGGG GGGCCAGAAGCGCCGGGCGCGCGCCTGGGGGGGGGGGCACGCGCGCGAGACGACGGGGCCAGGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:170357336..170357553 26863196 MeRIP-seq:(Medium) rs1291419600 Functional Loss SNV dbSNP153 33..33 33 - - - 82468 RMVar_ID_82468 Human_SNP_ID_163014392 m1A Human chr3 + 170357440 170357440 170357440 GGGGCCAGGGGGGCGCTCTGAGGAGCCACAATAGGCCAGACGGCACGCGCGTCCACGAGGGGGCC GGGGCCAGGGGGGCGCTCTGAGGAGCCACAATCGGCCAGACGGCACGCGCGTCCACGAGGGGGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:170357398..170357495 26863196 MeRIP-seq:(Medium) rs1314227190 Functional Loss SNV dbSNP153 33..33 33 - - - 82469 RMVar_ID_82469 Human_SNP_ID_163014393 m1A Human chr3 + 170357440 170357440 170357440 GGGGCCAGGGGGGCGCTCTGAGGAGCCACAATAGGCCAGACGGCACGCGCGTCCACGAGGGGGCC GGGGCCAGGGGGGCGCTCTGAGGAGCCACAATGGGCCAGACGGCACGCGCGTCCACGAGGGGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:170357398..170357495 26863196 MeRIP-seq:(Medium) rs1314227190 Functional Loss SNV dbSNP153 33..33 33 - - - 82470 RMVar_ID_82470 Human_SNP_ID_163014571 m1A Human chr3 + 170357742 170357736 170357742 CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG CCGGCACAGCCGAAGGGAGCGGGCGAG______CGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG GCGGCGA G SKIL Ensembl:ENSG00000136603 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170357330..170358205 26863196 MeRIP-seq:(Medium) rs912288864 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_3721576,Human_RBP_ID_4757551 Human_Splice_Rec_506041,Human_Splice_Rec_506043,Human_Splice_Rec_506047,Human_Splice_Rec_506057 82471 RMVar_ID_82471 Human_SNP_ID_163014577 m1A Human chr3 + 170357742 170357739 170357742 CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG CCGGCACAGCCGAAGGGAGCGGGCGAGCGG___CGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG GCGA G SKIL Ensembl:ENSG00000136603 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170357330..170358205 26863196 MeRIP-seq:(Medium) rs1410705207 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3721576,Human_RBP_ID_4757551 Human_Splice_Rec_506041,Human_Splice_Rec_506043,Human_Splice_Rec_506047,Human_Splice_Rec_506057 82472 RMVar_ID_82472 Human_SNP_ID_163014587 m1A Human chr3 + 170357742 170357742 170357742 CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGGCGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG A G SKIL Ensembl:ENSG00000136603 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170357330..170358205 26863196 MeRIP-seq:(Medium) rs1293906106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721576,Human_RBP_ID_4757551 Human_Splice_Rec_506041,Human_Splice_Rec_506043,Human_Splice_Rec_506047,Human_Splice_Rec_506057 82473 RMVar_ID_82473 Human_SNP_ID_163014588 m1A Human chr3 + 170357742 170357742 170357742 CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG CCGGCACAGCCGAAGGGAGCGGGCGAGCGGCGTCGGCGGCGGCGGCGGGCACAGGTGCGGCTCCG A T SKIL Ensembl:ENSG00000136603 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170357330..170358205 26863196 MeRIP-seq:(Medium) rs1293906106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721576,Human_RBP_ID_4757551 Human_Splice_Rec_506041,Human_Splice_Rec_506043,Human_Splice_Rec_506047,Human_Splice_Rec_506057 82474 RMVar_ID_82474 Human_SNP_ID_163014597 m1A Human chr3 + 170357760 170357760 170357760 GCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCACAGGTGCGGCTCCGGCTTACGGCGGCGACGCG GCGGGCGAGCGGCGACGGCGGCGGCGGCGGGCCCAGGTGCGGCTCCGGCTTACGGCGGCGACGCG A C SKIL Ensembl:ENSG00000136603 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr3:170357605..170358068;chr3:170357742..170358007;chr3:170357735..170357948;chr3:170357318..170358194 26863196 MeRIP-seq:(Medium) rs931535668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721576 Human_Splice_Rec_506039,Human_Splice_Rec_506041,Human_Splice_Rec_506043,Human_Splice_Rec_506047,Human_Splice_Rec_506057 82475 RMVar_ID_82475 Human_SNP_ID_163014945 m1A Human chr3 + 170358494 170358494 170358494 TTAGAGATAGGTGGGTGGCTTTGAGTGGGCGGAGGACTTCAGGGTTTTAGGGGCTCCCCCATTCT TTAGAGATAGGTGGGTGGCTTTGAGTGGGCGGGGGACTTCAGGGTTTTAGGGGCTCCCCCATTCT A G SKIL Ensembl:ENSG00000136603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:170358487..170358616 26863196 MeRIP-seq:(Medium) rs946246860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3720949,Human_RBP_ID_7155504 82476 RMVar_ID_82476 Human_SNP_ID_163015391 m1A Human chr3 - 170359704 170359704 170359704 ATCTTCAAGGATTATAGTTCATTCTTCTTTTAATTAATCTGGAAGAAGAGAAGGGGGGTTGGGGA ATCTTCAAGGATTATAGTTCATTCTTCTTTTAGTTAATCTGGAAGAAGAGAAGGGGGGTTGGGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:170359698..170359805 26863196 MeRIP-seq:(Medium) rs1471012216 Functional Loss SNV dbSNP153 33..33 33 - - - 82477 RMVar_ID_82477 Human_SNP_ID_163127281 m1A Human chr3 - 170822153 170822153 170822153 CCTAGTCTCTGTGCCCAGTGAAACTCATCCCAAATCTTCCTTCTTTCCCTCTCGCCTGTCCCCTC CCTAGTCTCTGTGCCCAGTGAAACTCATCCCACATCTTCCTTCTTTCCCTCTCGCCTGTCCCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:170822089..170822188;chr3:170822105..170822218 26863196 MeRIP-seq:(Medium) rs1242282958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8565047 82478 RMVar_ID_82478 Human_SNP_ID_163139018 m1A Human chr3 - 170870089 170870089 170870089 AATTTAATGATTTCCGCTGTAACGATTTTTGCATCTGTCGAGTGGAGACGTCTCAGTCAAGATAA AATTTAATGATTTCCGCTGTAACGATTTTTGCGTCTGTCGAGTGGAGACGTCTCAGTCAAGATAA T C RPL22L1 Ensembl:ENSG00000163584 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:170870062..170870136 26863196 MeRIP-seq:(Medium) rs1209243148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933404,Human_RBP_ID_2765705,Human_RBP_ID_14721862,Human_RBP_ID_19120882 82479 RMVar_ID_82479 Human_SNP_ID_163204837 m1A Human chr3 - 171140507 171140507 171140507 CTTCATGGTTGTCTGCTTGTTGCCCCACAGCAACAAAGGCGAGAGAAGGAGCTGCGGAAGCAGCA CTTCATGGTTGTCTGCTTGTTGCCCCACAGCAGCAAAGGCGAGAGAAGGAGCTGCGGAAGCAGCA T C TNIK Ensembl:ENSG00000154310 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:171140361..171140554 26863196 MeRIP-seq:(Medium) rs1454535979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25768194 Human_Splice_Rec_506348,Human_Splice_Rec_506434,Human_Splice_Rec_506496,Human_Splice_Rec_506558,Human_Splice_Rec_506616,Human_Splice_Rec_506678,Human_Splice_Rec_506738,Human_Splice_Rec_506800 RMVar_hsa_circ_222652,RMVar_hsa_circ_79298,RMVar_hsa_circ_86580,RMVar_hsa_circ_222653,RMVar_hsa_circ_341823,RMVar_hsa_circ_367319,RMVar_hsa_circ_115106,RMVar_hsa_circ_104825,RMVar_hsa_circ_45519,RMVar_hsa_circ_342628,RMVar_hsa_circ_222655,RMVar_hsa_circ_278456,RMVar_hsa_circ_222656,RMVar_hsa_circ_222657 82480 RMVar_ID_82480 Human_SNP_ID_163208967 m1A Human chr3 - 171157494 171157494 171157494 GCAGCTGCTGGCCGAGCGTCAGAAGCGCATCGAGGAGCAGAAAGAGCAGAGGCGGCGGCTGGAGG GCAGCTGCTGGCCGAGCGTCAGAAGCGCATCGGGGAGCAGAAAGAGCAGAGGCGGCGGCTGGAGG T C TNIK Ensembl:ENSG00000154310 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:171140494..171157571 26863196 MeRIP-seq:(Medium) rs570387939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_506347,Human_Splice_Rec_506433,Human_Splice_Rec_506495,Human_Splice_Rec_506557,Human_Splice_Rec_506615,Human_Splice_Rec_506677,Human_Splice_Rec_506737,Human_Splice_Rec_506799 RMVar_hsa_circ_38053,RMVar_hsa_circ_222652,RMVar_hsa_circ_79298,RMVar_hsa_circ_86580,RMVar_hsa_circ_222653,RMVar_hsa_circ_341823,RMVar_hsa_circ_115106,RMVar_hsa_circ_104825,RMVar_hsa_circ_45519,RMVar_hsa_circ_222655,RMVar_hsa_circ_278456,RMVar_hsa_circ_222656,RMVar_hsa_circ_303017,RMVar_hsa_circ_330054,RMVar_hsa_circ_222657,RMVar_hsa_circ_338559,RMVar_hsa_circ_326762,RMVar_hsa_circ_277124,RMVar_hsa_circ_286135,RMVar_hsa_circ_66128,RMVar_hsa_circ_222660,RMVar_hsa_circ_222662,RMVar_hsa_circ_222664,RMVar_hsa_circ_222665,RMVar_hsa_circ_222663,RMVar_hsa_circ_222661,RMVar_hsa_circ_222658,RMVar_hsa_circ_222659 82481 RMVar_ID_82481 Human_SNP_ID_163305888 m1A Human chr3 - 171562624 171562605 171562624 GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAAAAGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAA___________________GAAAAGAAGAAGAA CTTCTTCTCTTCTTCTTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:171562565..171562696 26863196 MeRIP-seq:(Medium) rs1177624399 Functional Loss DEL dbSNP153 33..51 33 - - - 82482 RMVar_ID_82482 Human_SNP_ID_163305911 m1A Human chr3 - 171562624 171562622 171562624 GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAAAAGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAA__GAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:171562565..171562696 26863196 MeRIP-seq:(Medium) rs1296033469 Functional Loss DEL dbSNP153 33..34 33 - - - 82483 RMVar_ID_82483 Human_SNP_ID_163305912 m1A Human chr3 - 171562624 171562622 171562624 GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAAAAGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAA_AGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA CTT CT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:171562565..171562696 26863196 MeRIP-seq:(Medium) rs1296033469 Functional Loss DEL dbSNP153 33..33 33 - - - 82484 RMVar_ID_82484 Human_SNP_ID_163305915 m1A Human chr3 - 171562624 171562624 171562624 GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAAAAGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA GAGAAGAAGAAGAAAGAAGAAGAAGAGAAGAAGAGAAGAAGAAGAGAAGAAGAAAAGAAGAAGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:171562565..171562696 26863196 MeRIP-seq:(Medium) rs1192245388 Functional Loss SNV dbSNP153 33..33 33 - - - 82485 RMVar_ID_82485 Human_SNP_ID_163361117 m1A Human chr3 + 171797054 171797054 171797054 GTTAGTTTAACTTTCCAGCTCTCTCATTCTTAATTCCACCTGTTCATGGTTGTTCCTCCCCTCAC GTTAGTTTAACTTTCCAGCTCTCTCATTCTTATTTCCACCTGTTCATGGTTGTTCCTCCCCTCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:171796868..171797101 26863196 MeRIP-seq:(Medium) rs1224283022 Functional Loss SNV dbSNP153 33..33 33 - - - 82486 RMVar_ID_82486 Human_SNP_ID_163364090 m1A Human chr3 - 171810069 171810069 171810069 GTCCTCTGCAGGATGCACCGCCTCGCCGCCACAGGGCTTCGGGTGCAGTGTGTGTGGTGTCCCCA GTCCTCTGCAGGATGCACCGCCTCGCCGCCACGGGGCTTCGGGTGCAGTGTGTGTGGTGTCCCCA T C PLD1 Ensembl:ENSG00000075651 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:171810063..171810482 26863196 MeRIP-seq:(Medium) rs917848923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424341 82487 RMVar_ID_82487 Human_SNP_ID_163364199 m1A Human chr3 - 171810446 171810446 171810446 GCTCCAGCTGTGCCAGAGGCACCCGAGCCCTGAGAGTCCGCCGCCAACGCGCAGGTGCTAGCGGC GCTCCAGCTGTGCCAGAGGCACCCGAGCCCTGGGAGTCCGCCGCCAACGCGCAGGTGCTAGCGGC T C PLD1 Ensembl:ENSG00000075651 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:171810359..171810482 26863196 MeRIP-seq:(Medium) rs192558948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8875672 Human_Splice_Rec_506887,Human_Splice_Rec_506941,Human_Splice_Rec_507037,Human_Splice_Rec_507067,Human_Splice_Rec_507087,Human_Splice_Rec_507089 82488 RMVar_ID_82488 Human_SNP_ID_163420295 m1A Human chr3 + 172039651 172039622 172039651 ATTTGAGCGGCGGCGGCGGCGGCTGGAGGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAGGGGGCG ATTT_____________________________GAGCGGCGGCGGCGGGAGCAGCGAAGGGGGCG TGAGCGGCGGCGGCGGCGGCTGGAGGAGGA T FNDC3B Ensembl:ENSG00000075420 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:172039601..172039800 26863196 MeRIP-seq:(Medium) rs1226982559 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_18424085,Human_RBP_ID_27822696 RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702 82489 RMVar_ID_82489 Human_SNP_ID_163420314 m1A Human chr3 + 172039645 172039642 172039645 GTAGTTATTTGAGCGGCGGCGGCGGCGGCTGGAGGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAG GTAGTTATTTGAGCGGCGGCGGCGGCGGCT___GGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAG TGGA T FNDC3B Ensembl:ENSG00000075420 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:172039595..172039766 26863196 MeRIP-seq:(Medium) rs1208677695 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_18424085 RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702 82490 RMVar_ID_82490 Human_SNP_ID_163420318 m1A Human chr3 + 172039645 172039645 172039645 GTAGTTATTTGAGCGGCGGCGGCGGCGGCTGGAGGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAG GTAGTTATTTGAGCGGCGGCGGCGGCGGCTGGTGGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAG A T FNDC3B Ensembl:ENSG00000075420 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:172039595..172039766 26863196 MeRIP-seq:(Medium) rs976106474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424085 RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702 82491 RMVar_ID_82491 Human_SNP_ID_163420331 m1A Human chr3 + 172039675 172039675 172039675 GGAGGAGGAGAGCGGCGGCGGCGGGAGCAGCGAAGGGGGCGGCAGGGATCCTCCAGGCTGCCGGC GGAGGAGGAGAGCGGCGGCGGCGGGAGCAGCGGAGGGGGCGGCAGGGATCCTCCAGGCTGCCGGC A G FNDC3B Ensembl:ENSG00000075420 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:172039576..172039817 26863196 MeRIP-seq:(Medium) rs1042985660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934548,Human_RBP_ID_3964340,Human_RBP_ID_9333942,Human_RBP_ID_18424085,Human_RBP_ID_27822696 Human_Splice_Rec_507151,Human_Splice_Rec_507201,Human_Splice_Rec_507207 RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702 82492 RMVar_ID_82492 Human_SNP_ID_163420597 m1A Human chr3 + 172040455 172040455 172040455 GACACTCCCCGCCCCGCTGCTGGCCACCTCCGAGCACGCCACGTCCTCCTCCCCGTCCTGCCCCC GACACTCCCCGCCCCGCTGCTGGCCACCTCCGGGCACGCCACGTCCTCCTCCCCGTCCTGCCCCC A G FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:172040451..172040805 26863196 MeRIP-seq:(Medium) rs1279334847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3722241 RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702 82493 RMVar_ID_82493 Human_SNP_ID_163420627 m1A Human chr3 - 172040551 172040530 172040551 CCGCCGCGCCCCGCTCCCCCGCCCGAGCTTCCAGCCGCCGGCTCGCCAAGTCCGGCCGCGGCCGC CCGCCGCGCCCCGCTCCCCCGCCCGAGCTTCC_____________________GGCCGCGGCCGC CGGACTTGGCGAGCCGGCGGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:172040525..172040819 26863196 MeRIP-seq:(Medium) rs886746142 Functional Loss DEL dbSNP153 33..53 33 - - - 82494 RMVar_ID_82494 Human_SNP_ID_163472640 m1A Human chr3 - 172262085 172262069 172262085 GCTCCTTTCATTCCACTTGTTTTCCTGTTCTTACCACTTCCTTTTATTTCAATGTGCCATTCCTC GCTCCTTTCATTCCACTTGTTTTCCTGTTCTT________________TCAATGTGCCATTCCTC AAATAAAAGGAAGTGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:172262066..172262155 26863196 MeRIP-seq:(Medium) rs1225446050 Functional Loss DEL dbSNP153 33..48 33 - - - 82495 RMVar_ID_82495 Human_SNP_ID_163488944 m1A Human chr3 - 172330681 172330681 172330681 TTTCATCCTCCTGAATTTCCAAGGTGTAGGTGATCACTTCCTCGGGTGAACAGCCTTCTGGCTTA TTTCATCCTCCTGAATTTCCAAGGTGTAGGTGTTCACTTCCTCGGGTGAACAGCCTTCTGGCTTA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:172330572..172334963 32194978 MeRIP-seq:(Medium) rs763873698 Functional Loss SNV dbSNP153 33..33 33 - - - 82496 RMVar_ID_82496 Human_SNP_ID_163504974 m1A Human chr3 + 172397383 172397383 172397383 TAGATGATCCCAAAATGAAGAGCATGATGCCTACTGATGAACAGTTTGCAGCCATCATTGTGCTT TAGATGATCCCAAAATGAAGAGCATGATGCCTGCTGATGAACAGTTTGCAGCCATCATTGTGCTT A G FNDC3B Ensembl:ENSG00000075420 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:172397274..172397425 32194978 MeRIP-seq:(Medium) rs140266078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18802299 RMVar_hsa_circ_121390,RMVar_hsa_circ_222708,RMVar_hsa_circ_86500,RMVar_hsa_circ_222729,RMVar_hsa_circ_92957,RMVar_hsa_circ_222759 82497 RMVar_ID_82497 Human_SNP_ID_163582043 m1A Human chr3 - 172701280 172701280 172701280 ACTCCTGGGACAGATTCTGGAATAGCTGGGTGAATGGGGACCATGACCCTGATTTGGGAGCAAGA ACTCCTGGGACAGATTCTGGAATAGCTGGGTGGATGGGGACCATGACCCTGATTTGGGAGCAAGA T C NCEH1 Ensembl:ENSG00000144959 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:172701274..172701375 26863196 MeRIP-seq:(Medium) rs1374487363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2766950 82498 RMVar_ID_82498 Human_SNP_ID_163594712 m1A Human chr3 - 172750799 172750799 172750799 CACCTCTTCAAACGCCGACTCCTCTCACAAATACCGCCATTCCTCGCCGGCGGCCGCCACAACCG CACCTCTTCAAACGCCGACTCCTCTCACAAATCCCGCCATTCCTCGCCGGCGGCCGCCACAACCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:172750701..172750928 26863196 MeRIP-seq:(Medium) rs1003971799 Functional Loss SNV dbSNP153 33..33 33 - - - 82499 RMVar_ID_82499 Human_SNP_ID_163595461 m1A Human chr3 - 172753643 172753643 172753643 CTCCACCTATCTTGTCTTCCAACCCCCAATCCAACACTCTTGACTCATCCTCTGTGGATGTCTCT CTCCACCTATCTTGTCTTCCAACCCCCAATCCCACACTCTTGACTCATCCTCTGTGGATGTCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:172753641..172753754 26863196 MeRIP-seq:(Medium) rs1034471511 Functional Loss SNV dbSNP153 33..33 33 - - - 82500 RMVar_ID_82500 Human_SNP_ID_163595469 m1A Human chr3 + 172753681 172753681 172753681 GGGGGTTGGAAGACAAGATAGGTGGAGAGTCGAGCACTAAATGCAAATAGATGTGATGTAAATTA GGGGGTTGGAAGACAAGATAGGTGGAGAGTCGGGCACTAAATGCAAATAGATGTGATGTAAATTA A G ECT2 Ensembl:ENSG00000114346 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:172753679..172753746 26863196 MeRIP-seq:(Medium) rs1230490602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95318,RMVar_hsa_circ_222768 82501 RMVar_ID_82501 Human_SNP_ID_163995232 m1A Human chr3 + 174444151 174444151 174444151 GCCAATAGAGAACAAAAAATTGATGATGCAGGAGACAGAGGGGAATGCTGTTCACGAGGAGGTGA GCCAATAGAGAACAAAAAATTGATGATGCAGGGGACAGAGGGGAATGCTGTTCACGAGGAGGTGA A G NAALADL2 Ensembl:ENSG00000177694 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:174444057..174444281 26863196 MeRIP-seq:(Medium) rs1463847393 Functional Loss SNV dbSNP153 33..33 33 - - - 82502 RMVar_ID_82502 Human_SNP_ID_164661062 m1A Human chr3 - 177056805 177056805 177056805 GCATCTACAGATGGTAGAGTGGTAGGATTTGGAGTAGGATGGTAGGATTTGGTAAATTGTCAAAT GCATCTACAGATGGTAGAGTGGTAGGATTTGGTGTAGGATGGTAGGATTTGGTAAATTGTCAAAT T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:177056798..177056890 26863196 MeRIP-seq:(Medium) rs978751575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7160837,Human_RBP_ID_14731077,Human_RBP_ID_23985931 RMVar_hsa_circ_106698,RMVar_hsa_circ_125534,RMVar_hsa_circ_122616,RMVar_hsa_circ_100512,RMVar_hsa_circ_222820,RMVar_hsa_circ_222818,RMVar_hsa_circ_222819,RMVar_hsa_circ_315475,RMVar_hsa_circ_222817,RMVar_hsa_circ_293260,RMVar_hsa_circ_222828,RMVar_hsa_circ_222827,RMVar_hsa_circ_376182,RMVar_hsa_circ_36529,RMVar_hsa_circ_58371,RMVar_hsa_circ_222836,RMVar_hsa_circ_315740,RMVar_hsa_circ_79318,RMVar_hsa_circ_222838,RMVar_hsa_circ_302135,RMVar_hsa_circ_356813,RMVar_hsa_circ_222839,RMVar_hsa_circ_222842,RMVar_hsa_circ_222840,RMVar_hsa_circ_222841,RMVar_hsa_circ_360716,RMVar_hsa_circ_101123,RMVar_hsa_circ_360591,RMVar_hsa_circ_274982,RMVar_hsa_circ_98306,RMVar_hsa_circ_222843,RMVar_hsa_circ_375214,RMVar_hsa_circ_375656,RMVar_hsa_circ_222845,RMVar_hsa_circ_222846,RMVar_hsa_circ_101071,RMVar_hsa_circ_222847,RMVar_hsa_circ_222848 82503 RMVar_ID_82503 Human_SNP_ID_164693209 m1A Human chr3 + 177170155 177170155 177170155 CTGAATCCCAATGCATTCTCCAAGGTGCTGCCAGGGTTATCTGATTACACTGCAGCCCCACTCAA CTGAATCCCAATGCATTCTCCAAGGTGCTGCCCGGGTTATCTGATTACACTGCAGCCCCACTCAA A C RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:177170151..177170407 26863196 MeRIP-seq:(Medium) rs927719894 Functional Loss SNV dbSNP153 33..33 33 - - - 82504 RMVar_ID_82504 Human_SNP_ID_164701290 m1A Human chr3 + 177195312 177195312 177195312 GGCATACTTTCTTCCTGCAGCCCCTCCCCCACAGGTAAATGCTAACTATTTCTAGAACTCTCAAC GGCATACTTTCTTCCTGCAGCCCCTCCCCCACGGGTAAATGCTAACTATTTCTAGAACTCTCAAC A G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:177195310..177195403 26863196 MeRIP-seq:(Medium) rs1181810293 Functional Loss SNV dbSNP153 33..33 33 - - - 82505 RMVar_ID_82505 Human_SNP_ID_164701650 m1A Human chr3 + 177196408 177196408 177196408 CTGAACCCAACTTCAAAGAGCCTCCACCAAATACCTCCTTAAGACGATAAAAAGCACTAAGTTAC CTGAACCCAACTTCAAAGAGCCTCCACCAAATGCCTCCTTAAGACGATAAAAAGCACTAAGTTAC A G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:177196406..177196483 26863196 MeRIP-seq:(Medium) rs1421205041 Functional Loss SNV dbSNP153 33..33 33 - - - 82506 RMVar_ID_82506 Human_SNP_ID_164702025 m1A Human chr3 - 177197185 177197185 177197185 GGTGGTTGGAGGCGGTGGCGGCGGCGGCGAGGAGGGGAATTTCCTTGTGCCTCCATTCCCGGGAG GGTGGTTGGAGGCGGTGGCGGCGGCGGCGAGGGGGGGAATTTCCTTGTGCCTCCATTCCCGGGAG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:177197101..177197250 26863196 MeRIP-seq:(Medium) rs1173105258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836849,Human_RBP_ID_4731512,Human_RBP_ID_5325737,Human_RBP_ID_9333946,Human_RBP_ID_14734260,Human_RBP_ID_18424095,Human_RBP_ID_18953940,Human_RBP_ID_23020477,Human_RBP_ID_25768396,Human_RBP_ID_26825072,Human_RBP_ID_27049269 Human_Splice_Rec_508085,Human_Splice_Rec_508169,Human_Splice_Rec_508227,Human_Splice_Rec_508255,Human_Splice_Rec_508325,Human_Splice_Rec_508349,Human_Splice_Rec_508357,Human_Splice_Rec_508367,Human_Splice_Rec_508377,Human_Splice_Rec_508397,Human_Splice_Rec_508403,Human_Splice_Rec_508413,Human_Splice_Rec_508437 RMVar_hsa_circ_100512,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848 82507 RMVar_ID_82507 Human_SNP_ID_164702086 m1A Human chr3 + 177197309 177197309 177197309 GGGGGATGGGCGCCGGGCGGGCGGGGGCGGGGAGCGCGGCGCGGGTCCCCAGGTGGCGAGCGGAG GGGGGATGGGCGCCGGGCGGGCGGGGGCGGGGGGCGCGGCGCGGGTCCCCAGGTGGCGAGCGGAG A G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:177197251..177197439 26863196 MeRIP-seq:(Medium) rs1366879556 Functional Loss SNV dbSNP153 33..33 33 - - - 82508 RMVar_ID_82508 Human_SNP_ID_164702092 m1A Human chr3 + 177197327 177197327 177197327 GGGCGGGGGCGGGGAGCGCGGCGCGGGTCCCCAGGTGGCGAGCGGAGGTGCTCCCGCCGCGGGGG GGGCGGGGGCGGGGAGCGCGGCGCGGGTCCCCTGGTGGCGAGCGGAGGTGCTCCCGCCGCGGGGG A T RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:177197240..177197390 26863410 MeRIP-seq:(Medium) rs1401886407 Functional Loss SNV dbSNP153 33..33 33 - - - 82509 RMVar_ID_82509 Human_SNP_ID_164702108 m1A Human chr3 + 177197361 177197361 177197361 GTGGCGAGCGGAGGTGCTCCCGCCGCGGGGGGAGGGGCGGGGGCGCACGCGGCCGGCGGCGGGGG GTGGCGAGCGGAGGTGCTCCCGCCGCGGGGGGGGGGGCGGGGGCGCACGCGGCCGGCGGCGGGGG A G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:177197278..177197364 26863410 MeRIP-seq:(Medium) rs953851176 Functional Loss SNV dbSNP153 33..33 33 - - - 82510 RMVar_ID_82510 Human_SNP_ID_164702109 m1A Human chr3 + 177197361 177197361 177197361 GTGGCGAGCGGAGGTGCTCCCGCCGCGGGGGGAGGGGCGGGGGCGCACGCGGCCGGCGGCGGGGG GTGGCGAGCGGAGGTGCTCCCGCCGCGGGGGGTGGGGCGGGGGCGCACGCGGCCGGCGGCGGGGG A T RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:177197278..177197364 26863410 MeRIP-seq:(Medium) rs953851176 Functional Loss SNV dbSNP153 33..33 33 - - - 82511 RMVar_ID_82511 Human_SNP_ID_164702150 m1A Human chr3 - 177197434 177197434 177197434 TCCCTTAGTAACAGCTTTTACCTTCTGCCTCAATTCCTCTCCCCGCTCGCGCCCTTCCCCCGCGC TCCCTTAGTAACAGCTTTTACCTTCTGCCTCAGTTCCTCTCCCCGCTCGCGCCCTTCCCCCGCGC T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:177197384..177197561 26863196 MeRIP-seq:(Medium) rs1260883763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_595348,Human_RBP_ID_5505885 82512 RMVar_ID_82512 Human_SNP_ID_165051346 m1A Human chr3 - 178637479 178637479 178637479 AATGTTATTAGATACTAATGAAGAACCTTCTCACCACTCCCTTCCAGTGTCCAAGTTCTGCTGTG AATGTTATTAGATACTAATGAAGAACCTTCTCTCCACTCCCTTCCAGTGTCCAAGTTCTGCTGTG T A KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:178637474..178637601 26863196 MeRIP-seq:(Medium) rs977211979 Functional Loss SNV dbSNP153 33..33 33 - - - 82513 RMVar_ID_82513 Human_SNP_ID_165059689 m1A Human chr3 - 178674052 178674052 178674052 AGTAATTGATGGATGAAGAGGGGACAGAGTCAATGGTGTCAAATGTTTCTGAGATATAAAGAAAA AGTAATTGATGGATGAAGAGGGGACAGAGTCAGTGGTGTCAAATGTTTCTGAGATATAAAGAAAA T C KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:178674049..178674191 26863196 MeRIP-seq:(Medium) rs911104961 Functional Loss SNV dbSNP153 33..33 33 - - - 82514 RMVar_ID_82514 Human_SNP_ID_165085567 m1A Human chr3 - 178771815 178771814 178771815 GATAAATAAATAAGGGATCTGGCCATGAGATCAGGGGTAAGGGATCTGGTGGTGAGGTAAGCAAG GATAAATAAATAAGGGATCTGGCCATGAGATC_GGGGTAAGGGATCTGGTGGTGAGGTAAGCAAG CT C KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:178771765..178772002 26863196 MeRIP-seq:(Medium) rs1379384702 Functional Loss DEL dbSNP153 33..33 33 - - - 82515 RMVar_ID_82515 Human_SNP_ID_165085596 m1A Human chr3 - 178771943 178771943 178771943 AGAAATTTAGCAATGAGGTAAGGAGGTAAGGGATCTGGTCATGAGGTAAGGAGGTAAGGGATCTC AGAAATTTAGCAATGAGGTAAGGAGGTAAGGGTTCTGGTCATGAGGTAAGGAGGTAAGGGATCTC T A KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:178771831..178771965 26863196 MeRIP-seq:(Medium) rs1446082243 Functional Loss SNV dbSNP153 33..33 33 - - - 82516 RMVar_ID_82516 Human_SNP_ID_165096551 m1A Human chr3 - 178819442 178819440 178819442 GAGGGTGTCTGGGACAAGAGATGGAAAGACAGAGGGGCGGAGAGATTGAGAGACAATGGCTGCAG GAGGGTGTCTGGGACAAGAGATGGAAAGACAG__GGGCGGAGAGATTGAGAGACAATGGCTGCAG CCT C KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:178819392..178819483 26863196 MeRIP-seq:(Medium) rs1264311397 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5606995 RMVar_hsa_circ_125376,RMVar_hsa_circ_222862 82517 RMVar_ID_82517 Human_SNP_ID_165096557 m1A Human chr3 + 178819467 178819467 178819467 CCGCCCCTCTGTCTTTCCATCTCTTGTCCCAGACACCCTCGGCCTCCAGTCTCCCTTCCTCTCTG CCGCCCCTCTGTCTTTCCATCTCTTGTCCCAGTCACCCTCGGCCTCCAGTCTCCCTTCCTCTCTG A T KCNMB2,AC117457.1 Ensembl:ENSG00000197584,Ensembl:ENSG00000275163 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:178819367..178819543 26863196 MeRIP-seq:(Medium) rs921923758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36283 82518 RMVar_ID_82518 Human_SNP_ID_165139545 m1A Human chr3 - 179003228 179003224 179003229 TGAATACATGGAGGTATAGTACAAAAACACATAACAGAGGCTGGGAAGAGTGAATGGTAGGGAGA TGAATACATGGAGGTATAGTACAAAAACACA_____GAGGCTGGGAAGAGTGAATGGTAGGGAGA CTGTTA C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:179003178..179003265 26863196 MeRIP-seq:(Medium) rs961912683 Functional Loss DEL dbSNP153 32..36 33 - - - 82519 RMVar_ID_82519 Human_SNP_ID_165142746 m1A Human chr3 - 179017424 179017424 179017424 AAAACCAATCAACTGTGAATTGTGAAATTGAAACTACTCTTTCGGTTTTATTTTCTTTAGCATAT AAAACCAATCAACTGTGAATTGTGAAATTGAAGCTACTCTTTCGGTTTTATTTTCTTTAGCATAT T C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1956366,Human_RBP_ID_18335666,Human_RBP_ID_26505716 Human_miRNA_ID_855928 GWAS_ID_9625,GWAS_ID_9626,GWAS_ID_9627 RMVar_hsa_circ_120479,RMVar_hsa_circ_222868,RMVar_hsa_circ_107005,RMVar_hsa_circ_222867 82520 RMVar_ID_82520 Human_SNP_ID_165150052 m1A Human chr3 + 179046896 179046895 179046896 AGACTGACCTCAGACATGCCTAACCCTGCCCCAACCCGATGGTCTTCTCTACCCACACTGGTGGC AGACTGACCTCAGACATGCCTAACCCTGCCCC_ACCCGATGGTCTTCTCTACCCACACTGGTGGC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:179046892..179047022 26863196 MeRIP-seq:(Medium) rs1477441105 Functional Loss DEL dbSNP153 33..33 33 - - - 82521 RMVar_ID_82521 Human_SNP_ID_165155972 m1A Human chr3 - 179071738 179071738 179071738 ACTGACTTTTGACAGTCAGCCTTCGGCTGCGGAGGGGGCTCGGCGGCGGCCGGCGGAGAAAGTTG ACTGACTTTTGACAGTCAGCCTTCGGCTGCGGTGGGGGCTCGGCGGCGGCCGGCGGAGAAAGTTG T A ZMAT3 Ensembl:ENSG00000172667 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:179071570..179071800 26863196 MeRIP-seq:(Medium) rs370954576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784000,Human_RBP_ID_836650,Human_RBP_ID_4731595,Human_RBP_ID_5473987,Human_RBP_ID_5505896 RMVar_hsa_circ_103963,RMVar_hsa_circ_222869 82522 RMVar_ID_82522 Human_SNP_ID_165174888 m1A Human chr3 + 179148333 179148333 179148333 GGCGGGGGCGTGTGGCGGGGGCTAGCGAGGAGAGGGAGCGAGAAGTAGAAAGCGGCAGTTCCGGT GGCGGGGGCGTGTGGCGGGGGCTAGCGAGGAGGGGGAGCGAGAAGTAGAAAGCGGCAGTTCCGGT A G PIK3CA Ensembl:ENSG00000121879 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:179148283..179148541 26863196 MeRIP-seq:(Medium) rs1412777761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3720971,Human_RBP_ID_4756834,Human_RBP_ID_8235852,Human_RBP_ID_9434965,Human_RBP_ID_17671213,Human_RBP_ID_22606975,Human_RBP_ID_23026407 82523 RMVar_ID_82523 Human_SNP_ID_165276197 m1A Human chr3 - 179563000 179563000 179563000 CGACTGCGAGTCTCGAGGAGCGATAGCCCCTGACTCCCTTAACTTCCACCGCCACCCACCTCAGG CGACTGCGAGTCTCGAGGAGCGATAGCCCCTGCCTCCCTTAACTTCCACCGCCACCCACCTCAGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:179562926..179563125 26863196 MeRIP-seq:(Medium) rs1390963505 Functional Loss SNV dbSNP153 33..33 33 - - - 82524 RMVar_ID_82524 Human_SNP_ID_165276237 m1A Human chr3 + 179563089 179563089 179563089 TTAGCCCTTAGGGTAGGAGTCGCGCCGGCAGCAGCCATGAGCGGCGGCGTGTACGGGGGAGGTGA TTAGCCCTTAGGGTAGGAGTCGCGCCGGCAGCGGCCATGAGCGGCGGCGTGTACGGGGGAGGTGA A G ACTL6A Ensembl:ENSG00000136518 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:179562926..179569875 26863196 MeRIP-seq:(Medium) rs1438015706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785362,Human_RBP_ID_4757569,Human_RBP_ID_5325364,Human_RBP_ID_7162852 Human_Splice_Rec_509281,Human_Splice_Rec_509307,Human_Splice_Rec_509321,Human_Splice_Rec_509355 82525 RMVar_ID_82525 Human_SNP_ID_165278003 m1A Human chr3 - 179570177 179570177 179570177 ATATTCTCCCTCGGAACACGCAGAGCATTAGTATCTATGTAGTAGGTGGGACCGCCTTGTTTGCC ATATTCTCCCTCGGAACACGCAGAGCATTAGTGTCTATGTAGTAGGTGGGACCGCCTTGTTTGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:179570141..179570241 32194978 MeRIP-seq:(Medium) rs755343269 Functional Loss SNV dbSNP153 33..33 33 - - - 82526 RMVar_ID_82526 Human_SNP_ID_165282181 m1A Human chr3 - 179588048 179588048 179588048 TTTTCCTGAGTATACTAAAGCTATGAAACGTAAGGTGACAAAAGGAAGGTAGAAGCTTGGGAACT TTTTCCTGAGTATACTAAAGCTATGAAACGTACGGTGACAAAAGGAAGGTAGAAGCTTGGGAACT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:179588010..179588110 32194978 MeRIP-seq:(Medium) rs752060094 Functional Loss SNV dbSNP153 33..33 33 - - - 82527 RMVar_ID_82527 Human_SNP_ID_165282247 m1A Human chr3 - 179588342 179588342 179588342 CTGTAAGCCTAAGGTAAAAAGCATAGGCAGTAACTTTTACTAGTCAATAAAAAGCAGTTCTACCA CTGTAAGCCTAAGGTAAAAAGCATAGGCAGTAGCTTTTACTAGTCAATAAAAAGCAGTTCTACCA T C MRPL47 Ensembl:ENSG00000136522 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:179588258..179588358 32194978 MeRIP-seq:(Medium) rs1288477516 Functional Loss SNV dbSNP153 33..33 33 - - - 82528 RMVar_ID_82528 Human_SNP_ID_165286400 m1A Human chr3 - 179604589 179604589 179604589 GCTGCGGCCGGTTTGGCCCTTCTTTGTAGGAGAGTTTCATCCGCCCTGAAATCTTCCCGATCGTT GCTGCGGCCGGTTTGGCCCTTCTTTGTAGGAGGGTTTCATCCGCCCTGAAATCTTCCCGATCGTT T C MRPL47 Ensembl:ENSG00000136522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:179604490..179604603 26863196 MeRIP-seq:(Medium) rs1490249528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1622825,Human_RBP_ID_1956579,Human_RBP_ID_4757571,Human_RBP_ID_9334344,Human_RBP_ID_22092595,Human_RBP_ID_22509158,Human_RBP_ID_23213647,Human_RBP_ID_23987000 Human_Splice_Rec_509401,Human_Splice_Rec_509413,Human_Splice_Rec_509425 Human_miRNA_ID_2352952 RMVar_hsa_circ_126809,RMVar_hsa_circ_222936 82529 RMVar_ID_82529 Human_SNP_ID_165286556 m1A Human chr3 - 179604854 179604854 179604854 CCAAGGGGCCGGCCAGACAGAGCTGCCACCGCAGTAACCGAAACCCGCCGCAACAAACTCATGGC CCAAGGGGCCGGCCAGACAGAGCTGCCACCGCGGTAACCGAAACCCGCCGCAACAAACTCATGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:179604801..179605001 26863196 MeRIP-seq:(Medium) rs771190682 Functional Loss SNV dbSNP153 33..33 33 - - - 82530 RMVar_ID_82530 Human_SNP_ID_165286557 m1A Human chr3 - 179604854 179604854 179604854 CCAAGGGGCCGGCCAGACAGAGCTGCCACCGCAGTAACCGAAACCCGCCGCAACAAACTCATGGC CCAAGGGGCCGGCCAGACAGAGCTGCCACCGCCGTAACCGAAACCCGCCGCAACAAACTCATGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:179604801..179605001 26863196 MeRIP-seq:(Medium) rs771190682 Functional Loss SNV dbSNP153 33..33 33 - - - 82531 RMVar_ID_82531 Human_SNP_ID_165286566 m1A Human chr3 + 179604863 179604863 179604863 TTGTTGCGGCGGGTTTCGGTTACTGCGGTGGCAGCTCTGTCTGGCCGGCCCCTTGGCACTCGCCT TTGTTGCGGCGGGTTTCGGTTACTGCGGTGGCGGCTCTGTCTGGCCGGCCCCTTGGCACTCGCCT A G NDUFB5 Ensembl:ENSG00000136521 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:179604801..179605050 26863196 MeRIP-seq:(Medium) rs1208464562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248302,Human_RBP_ID_595687,Human_RBP_ID_785364,Human_RBP_ID_4757572,Human_RBP_ID_5325365,Human_RBP_ID_9333952,Human_RBP_ID_17404772,Human_RBP_ID_22092018,Human_RBP_ID_22455638,Human_RBP_ID_27500030 Human_Splice_Rec_509435,Human_Splice_Rec_509441,Human_Splice_Rec_509449,Human_Splice_Rec_509455,Human_Splice_Rec_509465,Human_Splice_Rec_509475,Human_Splice_Rec_509483,Human_Splice_Rec_509493,Human_Splice_Rec_509495,Human_Splice_Rec_509507,Human_Splice_Rec_509515,Human_Splice_Rec_509519 Human_miRNA_ID_633920 82532 RMVar_ID_82532 Human_SNP_ID_165286567 m1A Human chr3 + 179604863 179604863 179604863 TTGTTGCGGCGGGTTTCGGTTACTGCGGTGGCAGCTCTGTCTGGCCGGCCCCTTGGCACTCGCCT TTGTTGCGGCGGGTTTCGGTTACTGCGGTGGCTGCTCTGTCTGGCCGGCCCCTTGGCACTCGCCT A T NDUFB5 Ensembl:ENSG00000136521 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:179604801..179605050 26863196 MeRIP-seq:(Medium) rs1208464562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248302,Human_RBP_ID_595687,Human_RBP_ID_785364,Human_RBP_ID_4757572,Human_RBP_ID_5325365,Human_RBP_ID_9333952,Human_RBP_ID_17404772,Human_RBP_ID_22092018,Human_RBP_ID_22455638,Human_RBP_ID_27500030 Human_Splice_Rec_509435,Human_Splice_Rec_509441,Human_Splice_Rec_509449,Human_Splice_Rec_509455,Human_Splice_Rec_509465,Human_Splice_Rec_509475,Human_Splice_Rec_509483,Human_Splice_Rec_509493,Human_Splice_Rec_509495,Human_Splice_Rec_509507,Human_Splice_Rec_509515,Human_Splice_Rec_509519 Human_miRNA_ID_633920 82533 RMVar_ID_82533 Human_SNP_ID_165286596 m1A Human chr3 - 179604900 179604900 179604900 CTTCGGAAAGCCACGAGTGAGGAAGCCCCCAAATCCGAGGCGAGTGCCAAGGGGCCGGCCAGACA CTTCGGAAAGCCACGAGTGAGGAAGCCCCCAAGTCCGAGGCGAGTGCCAAGGGGCCGGCCAGACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:179604850..179605113 26863196 MeRIP-seq:(Medium) rs749678949 Functional Loss SNV dbSNP153 33..33 33 - - - 82534 RMVar_ID_82534 Human_SNP_ID_165287704 m1A Human chr3 + 179609333 179609333 179609333 TTTACCAAGACAGTCATAGATACAGAGGACAGATTTATTAGAGAAAATACGAAGATAGAGTTGCA TTTACCAAGACAGTCATAGATACAGAGGACAGGTTTATTAGAGAAAATACGAAGATAGAGTTGCA A G NDUFB5 Ensembl:ENSG00000136521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:179609331..179609415 26863196 MeRIP-seq:(Medium) rs934533243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14737423 82535 RMVar_ID_82535 Human_SNP_ID_165288050 m1A Human chr3 + 179610982 179610982 179610982 GGGATAGTTTTAATAGGTGGAACTGGCAGAAAAGTAAAGGTTGAGTTTTTTTTATTGGATATGTG GGGATAGTTTTAATAGGTGGAACTGGCAGAAACGTAAAGGTTGAGTTTTTTTTATTGGATATGTG A C NDUFB5 Ensembl:ENSG00000136521 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:179610980..179611103 26863196 MeRIP-seq:(Medium) rs1211083982 Functional Loss SNV dbSNP153 33..33 33 - - - 82536 RMVar_ID_82536 Human_SNP_ID_165289010 m1A Human chr3 - 179614923 179614923 179614923 TACCCTGTTTTATACAAGGTTCATATGGGTATACTGTTATATTCTGAGTTAAAATCAGATTATAA TACCCTGTTTTATACAAGGTTCATATGGGTATTCTGTTATATTCTGAGTTAAAATCAGATTATAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:179614920..179614991 26863196 MeRIP-seq:(Medium) rs1202561935 Functional Loss SNV dbSNP153 33..33 33 - - - 82537 RMVar_ID_82537 Human_SNP_ID_165298492 m1A Human chr3 - 179652888 179652870 179652889 GGCCGGGCGCGGCGGCGGGGGGCGGAGGGCGAACCCCTGAGGCGTTGGCGCGGGAGCTCGAGCGG GGCCGGGCGCGGCGGCGGGGGGCGGAGGGCG___________________CGGGAGCTCGAGCGG GCGCCAACGCCTCAGGGGTT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:179652804..179652955 26863410 MeRIP-seq:(Medium) rs1560035041 Functional Loss DEL dbSNP153 32..50 33 - - - 82538 RMVar_ID_82538 Human_SNP_ID_165298603 m1A Human chr3 + 179653170 179653170 179653170 TCAGCCCGCTCGCTGGCGCCGCCGCCGCCGGCAGACCCCGCGCTCCGGCTCCGGCTCGGCTCGCT TCAGCCCGCTCGCTGGCGCCGCCGCCGCCGGCGGACCCCGCGCTCCGGCTCCGGCTCGGCTCGCT A G USP13 Ensembl:ENSG00000058056 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:179653080..179653177 26863410 MeRIP-seq:(Medium) rs552944493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2249937 RMVar_hsa_circ_86349,RMVar_hsa_circ_222944 82539 RMVar_ID_82539 Human_SNP_ID_165298676 m1A Human chr3 - 179653305 179653305 179653305 GCACGCGGATCGTGGGCATGTGGGGCACTAGCAGCTCGCCGATGTCTCCTGCAGCCATCTTCCTG GCACGCGGATCGTGGGCATGTGGGGCACTAGCCGCTCGCCGATGTCTCCTGCAGCCATCTTCCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:179652895..179653332 26863196 MeRIP-seq:(Medium) rs781272923 Functional Loss SNV dbSNP153 33..33 33 - - - 82540 RMVar_ID_82540 Human_SNP_ID_165315532 m1A Human chr3 - 179726247 179726247 179726247 TCTTGCTGCCCCAGGGCATGACAGACTTGCTCATGTCTCAAGGTCATGCCTTCTGCTGTCTTTTT TCTTGCTGCCCCAGGGCATGACAGACTTGCTCCTGTCTCAAGGTCATGCCTTCTGCTGTCTTTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:179726218..179726513 26863196 MeRIP-seq:(Medium) rs372515086 Functional Loss SNV dbSNP153 33..33 33 - - - 82541 RMVar_ID_82541 Human_SNP_ID_165328630 m1A Human chr3 - 179779032 179779032 179779032 CATGCTTGGCAAGCCCTGACCTTCAAGCTGTTATACCTTCAAGCCTTTATACCTACTGCTCTTTC CATGCTTGGCAAGCCCTGACCTTCAAGCTGTTGTACCTTCAAGCCTTTATACCTACTGCTCTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:179779027..179779110 26863196 MeRIP-seq:(Medium) rs1481918810 Functional Loss SNV dbSNP153 33..33 33 - - - 82542 RMVar_ID_82542 Human_SNP_ID_93093839 m1A Human chr2 + 135135797 135135797 135135797 TTTGAATGCCTAAGTGATACTGAAGAACTTAAAGGAAATGGACAAGAGAGTGGCAAGAAAGGAGG TTTGAATGCCTAAGTGATACTGAAGAACTTAACGGAAATGGACAAGAGAGTGGCAAGAAAGGAGG A C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:135135746..135135828 26863196 MeRIP-seq:(Medium) rs777263048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1898087,Human_RBP_ID_5588575,Human_RBP_ID_22078245,Human_RBP_ID_22981821,Human_RBP_ID_24546154,Human_RBP_ID_26339864,Human_RBP_ID_27818940 RMVar_hsa_circ_16664,RMVar_hsa_circ_58022,RMVar_hsa_circ_311022,RMVar_hsa_circ_349904,RMVar_hsa_circ_303978,RMVar_hsa_circ_203369,RMVar_hsa_circ_203368,RMVar_hsa_circ_203374,RMVar_hsa_circ_27431,RMVar_hsa_circ_203378,RMVar_hsa_circ_293723,RMVar_hsa_circ_346358,RMVar_hsa_circ_203379,RMVar_hsa_circ_370340,RMVar_hsa_circ_289131,RMVar_hsa_circ_32206,RMVar_hsa_circ_203381,RMVar_hsa_circ_330549,RMVar_hsa_circ_338356,RMVar_hsa_circ_203382,RMVar_hsa_circ_301742,RMVar_hsa_circ_268159,RMVar_hsa_circ_203384,RMVar_hsa_circ_68535 82543 RMVar_ID_82543 Human_SNP_ID_93097906 m1A Human chr2 + 135153784 135153784 135153784 AAGGAGAACTGAGTGCCCGGATGAAGATTCCAAGCAATATGTGGGTAGAAGCCTGGGAAACAGCT AAGGAGAACTGAGTGCCCGGATGAAGATTCCACGCAATATGTGGGTAGAAGCCTGGGAAACAGCT A C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:135153734..135153830 26863196 MeRIP-seq:(Medium) rs1477664568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58068,Human_RBP_ID_534818,Human_RBP_ID_1898096,Human_RBP_ID_5471278,Human_RBP_ID_17964194,Human_RBP_ID_18746347,Human_RBP_ID_23826138,Human_RBP_ID_26339867,Human_RBP_ID_27817607 Human_Splice_Rec_299481,Human_Splice_Rec_299527,Human_Splice_Rec_299575,Human_Splice_Rec_299623 Human_miRNA_ID_269053,Human_miRNA_ID_2048931 RMVar_hsa_circ_16664,RMVar_hsa_circ_58022,RMVar_hsa_circ_311022,RMVar_hsa_circ_349904,RMVar_hsa_circ_203368,RMVar_hsa_circ_27431,RMVar_hsa_circ_346358,RMVar_hsa_circ_203379,RMVar_hsa_circ_370340,RMVar_hsa_circ_32206,RMVar_hsa_circ_203381,RMVar_hsa_circ_330549,RMVar_hsa_circ_338356,RMVar_hsa_circ_268159,RMVar_hsa_circ_346813,RMVar_hsa_circ_326317 82544 RMVar_ID_82544 Human_SNP_ID_93190031 m1A Human chr2 + 135533825 135533825 135533825 CGCTTGAACCTGGGAGGCAGCGGTGAGCCGAGATCAGGCCATTGAACTCCAGTCTGGGCAACAAG CGCTTGAACCTGGGAGGCAGCGGTGAGCCGAGTTCAGGCCATTGAACTCCAGTCTGGGCAACAAG A T R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:135533823..135533888 26863196 MeRIP-seq:(Medium) rs1236235177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13619328 RMVar_hsa_circ_203406,RMVar_hsa_circ_97196 82545 RMVar_ID_82545 Human_SNP_ID_93233563 m1A Human chr2 + 135724075 135724075 135724075 GCTCCGGGACCCCCAGTCCCAACCACGTCGTCACCCCCTCTGCTGTGGCAGTGGGGACAACACTG GCTCCGGGACCCCCAGTCCCAACCACGTCGTCGCCCCCTCTGCTGTGGCAGTGGGGACAACACTG A G R3HDM1 Ensembl:ENSG00000048991 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:135724051..135724075 26863196 MeRIP-seq:(Medium) rs548074075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142252,Human_RBP_ID_17279139,Human_RBP_ID_17392800,Human_RBP_ID_17509753 Human_miRNA_ID_2271447 RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_203453,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_203465 82546 RMVar_ID_82546 Human_SNP_ID_93237641 m1A Human chr2 + 135741828 135741828 135741828 GTGCGGAGCCGGAGGTGGGGGCCGAACCAGCCAAGGTTGCGGGGGCCGCAGAGCCGGACGAAGAC GTGCGGAGCCGGAGGTGGGGGCCGAACCAGCCGAGGTTGCGGGGGCCGCAGAGCCGGACGAAGAC A G UBXN4 Ensembl:ENSG00000144224 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:135741700..135741962;chr2:135741691..135741950;chr2:135741678..135741947 26863196 MeRIP-seq:(Medium) rs1435543929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3959577,Human_RBP_ID_4622708,Human_RBP_ID_5322640,Human_RBP_ID_9330677,Human_RBP_ID_18421898,Human_RBP_ID_22076612 82547 RMVar_ID_82547 Human_SNP_ID_93237679 m1A Human chr2 + 135741895 135741895 135741895 AGGGCGGAGCCGGCTTCGGGACTGCGGAGACTACACACCGAGCGAGCGCCTGGGCCCGAAGGGAG AGGGCGGAGCCGGCTTCGGGACTGCGGAGACTGCACACCGAGCGAGCGCCTGGGCCCGAAGGGAG A G UBXN4 Ensembl:ENSG00000144224 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:135741776..135742025 26863196 MeRIP-seq:(Medium) rs769886564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364,Human_RBP_ID_243758,Human_RBP_ID_3959577,Human_RBP_ID_4582441,Human_RBP_ID_8852102,Human_RBP_ID_9384775,Human_RBP_ID_13621896,Human_RBP_ID_18412803,Human_RBP_ID_23826591,Human_RBP_ID_25464567 82548 RMVar_ID_82548 Human_SNP_ID_93244804 m1A Human chr2 - 135769825 135769825 135769825 GAGGACAAAACAATGCTAACTGCATGAACTTTACCTGTTCTTCCTCTTTTCTTTTCTCTTCTCTC GAGGACAAAACAATGCTAACTGCATGAACTTTTCCTGTTCTTCCTCTTTTCTTTTCTCTTCTCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:135769751..135769825;chr2:135769751..135772434;chr2:135769751..135772452 26863196 MeRIP-seq:(Medium) rs953940906 Functional Loss SNV dbSNP153 33..33 33 - - - 82549 RMVar_ID_82549 Human_SNP_ID_93245000 m1A Human chr2 + 135770693 135770693 135770693 ATGCTGGAGGAAAGAAACAGAGAGAAAGCAGAAGATAGGGCAGCTCGAGAACGTATAAAACAGCA ATGCTGGAGGAAAGAAACAGAGAGAAAGCAGACGATAGGGCAGCTCGAGAACGTATAAAACAGCA A C UBXN4 Ensembl:ENSG00000144224 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:135770551..135770750 26863196 MeRIP-seq:(Medium) rs748759954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830150,Human_RBP_ID_918787,Human_RBP_ID_5594702,Human_RBP_ID_13622713,Human_RBP_ID_17657743,Human_RBP_ID_18193545,Human_RBP_ID_22996878,Human_RBP_ID_23826649,Human_RBP_ID_24545859,Human_RBP_ID_26339886,Human_RBP_ID_27817614 Human_Splice_Rec_300265,Human_Splice_Rec_300297 Human_miRNA_ID_461951,Human_miRNA_ID_2240350,Human_miRNA_ID_2790713 RMVar_hsa_circ_324148,RMVar_hsa_circ_295365,RMVar_hsa_circ_102610,RMVar_hsa_circ_277775,RMVar_hsa_circ_284026,RMVar_hsa_circ_203472,RMVar_hsa_circ_203474,RMVar_hsa_circ_203476,RMVar_hsa_circ_65909,RMVar_hsa_circ_203475,RMVar_hsa_circ_203473,RMVar_hsa_circ_41961,RMVar_hsa_circ_358321,RMVar_hsa_circ_274740,RMVar_hsa_circ_302406,RMVar_hsa_circ_371040,RMVar_hsa_circ_107595,RMVar_hsa_circ_306465,RMVar_hsa_circ_68750,RMVar_hsa_circ_203477,RMVar_hsa_circ_203478,RMVar_hsa_circ_360061,RMVar_hsa_circ_347385,RMVar_hsa_circ_65561,RMVar_hsa_circ_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_305460,RMVar_hsa_circ_120252,RMVar_hsa_circ_203479,RMVar_hsa_circ_109501,RMVar_hsa_circ_203480,RMVar_hsa_circ_203481,RMVar_hsa_circ_203482 82550 RMVar_ID_82550 Human_SNP_ID_93268561 m1A Human chr2 - 135865134 135865134 135865134 TAGTTTGGGGGGAAAGAGCTCAGAGATGAGGAACAGACAGCTGAGAGCATTAAGAACCAAATGAC TAGTTTGGGGGGAAAGAGCTCAGAGATGAGGAGCAGACAGCTGAGAGCATTAAGAACCAAATGAC T C MCM6 Ensembl:ENSG00000076003 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:135865085..135865206 26863196 MeRIP-seq:(Medium) rs201902619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1578322,Human_RBP_ID_1898538,Human_RBP_ID_6827652,Human_RBP_ID_9296818,Human_RBP_ID_13623800,Human_RBP_ID_23826778 Human_Splice_Rec_300370 Human_miRNA_ID_2095991,Human_miRNA_ID_2997525 RMVar_hsa_circ_77594,RMVar_hsa_circ_340132,RMVar_hsa_circ_106311,RMVar_hsa_circ_203487,RMVar_hsa_circ_203489,RMVar_hsa_circ_203488,RMVar_hsa_circ_7530,RMVar_hsa_circ_40983,RMVar_hsa_circ_351536,RMVar_hsa_circ_361529,RMVar_hsa_circ_78303,RMVar_hsa_circ_203495,RMVar_hsa_circ_203493,RMVar_hsa_circ_203494,RMVar_hsa_circ_105342,RMVar_hsa_circ_317245,RMVar_hsa_circ_351842,RMVar_hsa_circ_63470,RMVar_hsa_circ_203496,RMVar_hsa_circ_299695,RMVar_hsa_circ_337590,RMVar_hsa_circ_311103,RMVar_hsa_circ_329407 82551 RMVar_ID_82551 Human_SNP_ID_93269476 m1A Human chr2 - 135868788 135868788 135868788 CGCATCAGTGGGCAGGTGGTGCGGACTCACCCAGTTCACCCAGAGCTTGTGAGCGGAACTTTTCT CGCATCAGTGGGCAGGTGGTGCGGACTCACCCCGTTCACCCAGAGCTTGTGAGCGGAACTTTTCT T G MCM6 Ensembl:ENSG00000076003 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:135868739..135870329 32194978 MeRIP-seq:(Medium) rs1343219625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8851557,Human_RBP_ID_9094390,Human_RBP_ID_17273690 Human_Splice_Rec_300364 Human_miRNA_ID_2423281,Human_miRNA_ID_2432941,Human_miRNA_ID_2779033 RMVar_hsa_circ_24295,RMVar_hsa_circ_106311,RMVar_hsa_circ_203487,RMVar_hsa_circ_7530,RMVar_hsa_circ_351536,RMVar_hsa_circ_361529,RMVar_hsa_circ_203495,RMVar_hsa_circ_203494,RMVar_hsa_circ_105342,RMVar_hsa_circ_317245,RMVar_hsa_circ_337590,RMVar_hsa_circ_311103,RMVar_hsa_circ_329407,RMVar_hsa_circ_33928,RMVar_hsa_circ_203497,RMVar_hsa_circ_47780,RMVar_hsa_circ_323181 82552 RMVar_ID_82552 Human_SNP_ID_93269494 m1A Human chr2 - 135868836 135868836 135868836 TTAAACAGGATTCGAGAGCTCACCTCATCCAGAATTGGTTTGCTCACTCGCATCAGTGGGCAGGT TTAAACAGGATTCGAGAGCTCACCTCATCCAGGATTGGTTTGCTCACTCGCATCAGTGGGCAGGT T C MCM6 Ensembl:ENSG00000076003 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:135868739..135868840 26863410 MeRIP-seq:(Medium) rs765366780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1578328,Human_RBP_ID_4582593,Human_RBP_ID_18746584 Human_Splice_Rec_300364 RMVar_hsa_circ_24295,RMVar_hsa_circ_106311,RMVar_hsa_circ_203487,RMVar_hsa_circ_7530,RMVar_hsa_circ_351536,RMVar_hsa_circ_361529,RMVar_hsa_circ_203495,RMVar_hsa_circ_203494,RMVar_hsa_circ_105342,RMVar_hsa_circ_317245,RMVar_hsa_circ_337590,RMVar_hsa_circ_311103,RMVar_hsa_circ_329407,RMVar_hsa_circ_33928,RMVar_hsa_circ_203497,RMVar_hsa_circ_47780,RMVar_hsa_circ_323181 82553 RMVar_ID_82553 Human_SNP_ID_93271354 m1A Human chr2 - 135876325 135876325 135876325 CGCGGCGGCAGCGGAGCCGGGCGCCGGCAGCCAGCACCTGGAGGTCCGCGACGAGGTGGCCGAGA CGCGGCGGCAGCGGAGCCGGGCGCCGGCAGCCCGCACCTGGAGGTCCGCGACGAGGTGGCCGAGA T G MCM6 Ensembl:ENSG00000076003 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:135876274..135876425 26863196 MeRIP-seq:(Medium) rs1483194687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4582610,Human_RBP_ID_8851558,Human_RBP_ID_9094397,Human_RBP_ID_9296823,Human_RBP_ID_9330682,Human_RBP_ID_22449987,Human_RBP_ID_26339893 Human_Splice_Rec_300359 Human_miRNA_ID_794457 82554 RMVar_ID_82554 Human_SNP_ID_93296740 m1A Human chr2 + 135985473 135985473 135985473 TCTTGCGGCTGGCGCTGGCGCTGGGCATCGGGACACGGAACTGGGCAGTGGACACCACCCTCCCT TCTTGCGGCTGGCGCTGGCGCTGGGCATCGGGGCACGGAACTGGGCAGTGGACACCACCCTCCCT A G DARS-AS1 Ensembl:ENSG00000231890 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:135985274..135985935;chr2:135985349..135985658;chr2:135985324..135985935;chr2:135985401..135985625 26863196 MeRIP-seq:(Medium) rs1464271071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_300513,Human_Splice_Rec_300519,Human_Splice_Rec_300525,Human_Splice_Rec_300527 82555 RMVar_ID_82555 Human_SNP_ID_93298623 m1A Human chr2 - 135993500 135993500 135993500 AGAGACTTTACATTTCTAACAAGTTCCCAGGTATATTCATTTGCTTGGACTGCCATAACAAAGTA AGAGACTTTACATTTCTAACAAGTTCCCAGGTTTATTCATTTGCTTGGACTGCCATAACAAAGTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:135993408..135993535 26863196 MeRIP-seq:(Medium) rs1361841696 Functional Loss SNV dbSNP153 33..33 33 - - - 82556 RMVar_ID_82556 Human_SNP_ID_93327284 m1A Human chr2 - 136118094 136118094 136118094 TAGCAAAGTGACGCCGAGGGCCTGAGTGCTCCAGTAGCCACCGCATCTGGAGAACCAGCGGTTAC TAGCAAAGTGACGCCGAGGGCCTGAGTGCTCCGGTAGCCACCGCATCTGGAGAACCAGCGGTTAC T C CXCR4 Ensembl:ENSG00000121966 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:136118026..136118150 26863196 MeRIP-seq:(Medium) rs1295261321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4582689,Human_RBP_ID_20436376,Human_RBP_ID_27475217 Human_Splice_Rec_300683 RMVar_hsa_circ_103588,RMVar_hsa_circ_203511 82557 RMVar_ID_82557 Human_SNP_ID_93902435 m1A Human chr2 - 138502016 138502016 138502016 CCCTGGGAGCCCGAGGCTGCGGTGGTGGCAGCAGGGGTGATGGCGGCAAGTCCCTGTGGCGGCCG CCCTGGGAGCCCGAGGCTGCGGTGGTGGCAGCTGGGGTGATGGCGGCAAGTCCCTGTGGCGGCCG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:138501965..138502135 26863196 MeRIP-seq:(Medium) rs1218941491 Functional Loss SNV dbSNP153 33..33 33 - - - 82558 RMVar_ID_82558 Human_SNP_ID_94331542 m1A Human chr2 - 140222152 140222152 140222152 CATAATCACTTGTTCTTTCATTAGGGACTTGTATGAATGGCCACATGAGGGTTCATCTCTCTCTT CATAATCACTTGTTCTTTCATTAGGGACTTGTGTGAATGGCCACATGAGGGTTCATCTCTCTCTT T C RF02541-013 RNACentral:URS000094AD41 rRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:140222134..140222217 26863196 MeRIP-seq:(Medium) rs556784313 Functional Loss SNV dbSNP153 33..33 33 - - - 82559 RMVar_ID_82559 Human_SNP_ID_94825732 m1A Human chr2 - 142130929 142130929 142130929 CACGCTCTGCCTCCTCTCTCCCGCACGCGCGCATCCCTCCACCTTCCACATCCTGCTCCAGGCAG CACGCTCTGCCTCCTCTCTCCCGCACGCGCGCGTCCCTCCACCTTCCACATCCTGCTCCAGGCAG T C LRP1B Ensembl:ENSG00000168702 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:142130879..142130957 26863196 MeRIP-seq:(Medium) rs1362492341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243144 RMVar_hsa_circ_77134,RMVar_hsa_circ_203611 82560 RMVar_ID_82560 Human_SNP_ID_95024610 m1A Human chr2 - 142933309 142933309 142933309 ACCTCAGCCCTGTCCTCACTCTCCCAGACCTCACCAAACCTTTCTCCCTCTATACTGACCAACAG ACCTCAGCCCTGTCCTCACTCTCCCAGACCTCCCCAAACCTTTCTCCCTCTATACTGACCAACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:142933298..142933498 26863196 MeRIP-seq:(Medium) rs557997688 Functional Loss SNV dbSNP153 33..33 33 - - - 82561 RMVar_ID_82561 Human_SNP_ID_95024708 m1A Human chr2 - 142933774 142933774 142933774 TTTTTGGACAGGCCCTTGCTCTTGACCTCAGTACCCTATCCCTAAAACCATCCACTCTCCTTCAA TTTTTGGACAGGCCCTTGCTCTTGACCTCAGTTCCCTATCCCTAAAACCATCCACTCTCCTTCAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:142933760..142933843 26863196 MeRIP-seq:(Medium) rs13034980 Functional Loss SNV dbSNP153 33..33 33 - - - 82562 RMVar_ID_82562 Human_SNP_ID_95341988 m1A Human chr2 + 144235730 144235730 144235730 GTCCCTTTACATATGTCCAATCTGGCTAATGCAGAGATACCTGTAAGATCACAAAAGACATAGTT GTCCCTTTACATATGTCCAATCTGGCTAATGCTGAGATACCTGTAAGATCACAAAAGACATAGTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:144235706..144235794 26863196 MeRIP-seq:(Medium) rs1302999300 Functional Loss SNV dbSNP153 33..33 33 - - - 82563 RMVar_ID_82563 Human_SNP_ID_95364914 m1A Human chr2 - 144332313 144332313 144332313 GCCGCGCTGCGCGGAGATCCCAGAGGGGCAGCAGCGGCGGCTGCGGCGCGGGGAGCCGGGGGCGG GCCGCGCTGCGCGGAGATCCCAGAGGGGCAGCGGCGGCGGCTGCGGCGCGGGGAGCCGGGGGCGG T C GTDC1 Ensembl:ENSG00000121964 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:144332301..144332589 26863196 MeRIP-seq:(Medium) rs1487606781 Functional Loss SNV dbSNP153 33..33 33 - - - 82564 RMVar_ID_82564 Human_SNP_ID_95365000 m1A Human chr2 + 144332498 144332498 144332498 CCCTCCTGGCCACCGGCGCGGCCCAGCCGGCGACGCGCTGACGCCGTGCCCCTCCCCCGCGGCCG CCCTCCTGGCCACCGGCGCGGCCCAGCCGGCGCCGCGCTGACGCCGTGCCCCTCCCCCGCGGCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:144332425..144332577 26863196 MeRIP-seq:(Medium) rs1445748985 Functional Loss SNV dbSNP153 33..33 33 - - - 82565 RMVar_ID_82565 Human_SNP_ID_95365002 m1A Human chr2 - 144332504 144332504 144332504 CCGCGGCGGCCGCGGGGGAGGGGCACGGCGTCAGCGCGTCGCCGGCTGGGCCGCGCCGGTGGCCA CCGCGGCGGCCGCGGGGGAGGGGCACGGCGTCGGCGCGTCGCCGGCTGGGCCGCGCCGGTGGCCA T C GTDC1 Ensembl:ENSG00000121964 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:144332326..144332589 26863196 MeRIP-seq:(Medium) rs1209773387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421903,Human_RBP_ID_22997457 Human_Splice_Rec_301721,Human_Splice_Rec_301783,Human_Splice_Rec_301851 82566 RMVar_ID_82566 Human_SNP_ID_95378599 m1A Human chr2 + 144389644 144389644 144389644 CCTCGAACTCCTCGTCGCCATCCTGTCTGCCCAGCTTCCCGTAGCCATCCTCGCCTTCTTTCTCG CCTCGAACTCCTCGTCGCCATCCTGTCTGCCCGGCTTCCCGTAGCCATCCTCGCCTTCTTTCTCG A G lnc-ARHGAP15-17 RNACentral:URS00008B93D0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:144389516..144389715 26863196 MeRIP-seq:(Medium) rs1553960747 Functional Loss SNV dbSNP153 33..33 33 - - - 82567 RMVar_ID_82567 Human_SNP_ID_95408530 m1A Human chr2 - 144517268 144517268 144517268 AGCCAATCCCAGGAGGAAAAACGGTAAGAAGCAGCCCGAACCAAACTTTTCCGGGCCACTACGCG AGCCAATCCCAGGAGGAAAAACGGTAAGAAGCCGCCCGAACCAAACTTTTCCGGGCCACTACGCG T G ZEB2 Ensembl:ENSG00000169554 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:144517140..144517343 26863196 MeRIP-seq:(Medium) rs753449937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22996880 RMVar_hsa_circ_1415,RMVar_hsa_circ_349459,RMVar_hsa_circ_203684 82568 RMVar_ID_82568 Human_SNP_ID_96214874 m1A Human chr2 + 147844441 147844441 147844441 TGCCGCCGCCGCCGCCGCCGCCGCTGCCGCCGAGCGTTCCTCCGCTGCGCCTGGCTTCCAGCTTC TGCCGCCGCCGCCGCCGCCGCCGCTGCCGCCGCGCGTTCCTCCGCTGCGCCTGGCTTCCAGCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:147844215..147844461 26863196 MeRIP-seq:(Medium) rs1232498883 Functional Loss SNV dbSNP153 33..33 33 - - - 82569 RMVar_ID_82569 Human_SNP_ID_96214947 m1A Human chr2 + 147844574 147844574 147844574 CGGAGCCCGGAGCTGGAGCCAGAGCCTGGACCAGAACTTGGCCGCCGCCTGCACCGCCGCCGCCG CGGAGCCCGGAGCTGGAGCCAGAGCCTGGACCGGAACTTGGCCGCCGCCTGCACCGCCGCCGCCG A G ACVR2A Ensembl:ENSG00000121989 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:147844523..147844660 26863196 MeRIP-seq:(Medium) rs1558955381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4582904,Human_RBP_ID_13630407 82570 RMVar_ID_82570 Human_SNP_ID_96257187 m1A Human chr2 + 148020703 148020703 148020703 TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGACTTCACCTGCCGCTGCGGACCGTACACAACCA TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGGCTTCACCTGCCGCTGCGGACCGTACACAACCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:148020670..148021604 26863196 MeRIP-seq:(Medium) rs897172 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_425,Clinvar_Rec_3738 GWAS_ID_9628,GWAS_ID_9629,GWAS_ID_9630,GWAS_ID_9631,GWAS_ID_9632,GWAS_ID_9633,GWAS_ID_9634,GWAS_ID_9635,GWAS_ID_9636,GWAS_ID_9637,GWAS_ID_9638,GWAS_ID_9639,GWAS_ID_9640,GWAS_ID_9641,GWAS_ID_9642,GWAS_ID_9643,GWAS_ID_9644,GWAS_ID_9645,GWAS_ID_9646,GWAS_ID_9647,GWAS_ID_9648,GWAS_ID_9649,GWAS_ID_9650,GWAS_ID_9651,GWAS_ID_9652,GWAS_ID_9653,GWAS_ID_9654,GWAS_ID_9655,GWAS_ID_9656,GWAS_ID_9657,GWAS_ID_9658,GWAS_ID_9659,GWAS_ID_9660,GWAS_ID_9661,GWAS_ID_9662,GWAS_ID_9663,GWAS_ID_9664,GWAS_ID_9665,GWAS_ID_9666,GWAS_ID_9667,GWAS_ID_9668,GWAS_ID_9669,GWAS_ID_9670,GWAS_ID_9671,GWAS_ID_9672,GWAS_ID_9673,GWAS_ID_9674,GWAS_ID_9675,GWAS_ID_9676,GWAS_ID_9677,GWAS_ID_9678,GWAS_ID_9679,GWAS_ID_9680,GWAS_ID_9681,GWAS_ID_9682,GWAS_ID_9683,GWAS_ID_9684,GWAS_ID_9685,GWAS_ID_9686,GWAS_ID_9687,GWAS_ID_9688,GWAS_ID_9689,GWAS_ID_9690,GWAS_ID_9691,GWAS_ID_9692,GWAS_ID_9693,GWAS_ID_9694,GWAS_ID_9695,GWAS_ID_9696,GWAS_ID_9697,GWAS_ID_9698,GWAS_ID_9699,GWAS_ID_9700,GWAS_ID_9701,GWAS_ID_9702,GWAS_ID_9703,GWAS_ID_9704,GWAS_ID_9705,GWAS_ID_9706,GWAS_ID_9707,GWAS_ID_9708,GWAS_ID_9709,GWAS_ID_9710,GWAS_ID_9711,GWAS_ID_9712,GWAS_ID_9713,GWAS_ID_9714,GWAS_ID_9715,GWAS_ID_9716,GWAS_ID_9717,GWAS_ID_9718,GWAS_ID_9719,GWAS_ID_9720,GWAS_ID_9721,GWAS_ID_9722,GWAS_ID_9723,GWAS_ID_9724,GWAS_ID_9725,GWAS_ID_9726,GWAS_ID_9727,GWAS_ID_9728,GWAS_ID_9729,GWAS_ID_9730,GWAS_ID_9731,GWAS_ID_9732,GWAS_ID_9733,GWAS_ID_9734,GWAS_ID_9735,GWAS_ID_9736,GWAS_ID_9737,GWAS_ID_9738,GWAS_ID_9739,GWAS_ID_9740,GWAS_ID_9741,GWAS_ID_9742,GWAS_ID_9743,GWAS_ID_9744,GWAS_ID_9745,GWAS_ID_9746,GWAS_ID_9747,GWAS_ID_9748,GWAS_ID_9749,GWAS_ID_9750,GWAS_ID_9751,GWAS_ID_9752,GWAS_ID_9753,GWAS_ID_9754,GWAS_ID_9755,GWAS_ID_9756,GWAS_ID_9757,GWAS_ID_9758,GWAS_ID_9759,GWAS_ID_9760,GWAS_ID_9761,GWAS_ID_9762,GWAS_ID_9763,GWAS_ID_9764,GWAS_ID_9765,GWAS_ID_9766,GWAS_ID_9767,GWAS_ID_9768,GWAS_ID_9769,GWAS_ID_9770,GWAS_ID_9771,GWAS_ID_9772,GWAS_ID_9773,GWAS_ID_9774,GWAS_ID_9775,GWAS_ID_9776,GWAS_ID_9777,GWAS_ID_9778,GWAS_ID_9779,GWAS_ID_9780,GWAS_ID_9781,GWAS_ID_9782,GWAS_ID_9783,GWAS_ID_9784,GWAS_ID_9785,GWAS_ID_9786,GWAS_ID_9787,GWAS_ID_9788,GWAS_ID_9789,GWAS_ID_9790,GWAS_ID_9791,GWAS_ID_9792,GWAS_ID_9793,GWAS_ID_9794,GWAS_ID_9795,GWAS_ID_9796,GWAS_ID_9797,GWAS_ID_9798,GWAS_ID_9799,GWAS_ID_9800,GWAS_ID_9801,GWAS_ID_9802,GWAS_ID_9803,GWAS_ID_9804,GWAS_ID_9805,GWAS_ID_9806,GWAS_ID_9807,GWAS_ID_9808,GWAS_ID_9809,GWAS_ID_9810,GWAS_ID_9811,GWAS_ID_9812,GWAS_ID_9813,GWAS_ID_9814,GWAS_ID_9815,GWAS_ID_9816,GWAS_ID_9817,GWAS_ID_9818,GWAS_ID_9819,GWAS_ID_9820,GWAS_ID_9821,GWAS_ID_9822,GWAS_ID_9823,GWAS_ID_9824,GWAS_ID_9825,GWAS_ID_9826,GWAS_ID_9827,GWAS_ID_9828,GWAS_ID_9829,GWAS_ID_9830,GWAS_ID_9831,GWAS_ID_9832,GWAS_ID_9833,GWAS_ID_9834,GWAS_ID_9835,GWAS_ID_9836,GWAS_ID_9837,GWAS_ID_9838,GWAS_ID_9839,GWAS_ID_9840,GWAS_ID_9841,GWAS_ID_9842,GWAS_ID_9843,GWAS_ID_9844,GWAS_ID_9845,GWAS_ID_9846,GWAS_ID_9847,GWAS_ID_9848,GWAS_ID_9849,GWAS_ID_9850,GWAS_ID_9851,GWAS_ID_9852,GWAS_ID_9853,GWAS_ID_9854,GWAS_ID_9855,GWAS_ID_9856,GWAS_ID_9857,GWAS_ID_9858,GWAS_ID_9859,GWAS_ID_9860,GWAS_ID_9861,GWAS_ID_9862,GWAS_ID_9863,GWAS_ID_9864,GWAS_ID_9865,GWAS_ID_9866,GWAS_ID_9867,GWAS_ID_9868,GWAS_ID_9869,GWAS_ID_9870,GWAS_ID_9871,GWAS_ID_9872,GWAS_ID_9873,GWAS_ID_9874,GWAS_ID_9875,GWAS_ID_9876,GWAS_ID_9877,GWAS_ID_9878,GWAS_ID_9879,GWAS_ID_9880,GWAS_ID_9881,GWAS_ID_9882,GWAS_ID_9883,GWAS_ID_9884,GWAS_ID_9885,GWAS_ID_9886,GWAS_ID_9887,GWAS_ID_9888,GWAS_ID_9889,GWAS_ID_9890,GWAS_ID_9891,GWAS_ID_9892,GWAS_ID_9893,GWAS_ID_9894,GWAS_ID_9895,GWAS_ID_9896,GWAS_ID_9897,GWAS_ID_9898,GWAS_ID_9899,GWAS_ID_9900,GWAS_ID_9901,GWAS_ID_9902,GWAS_ID_9903,GWAS_ID_9904,GWAS_ID_9905,GWAS_ID_9906,GWAS_ID_9907,GWAS_ID_9908,GWAS_ID_9909,GWAS_ID_9910,GWAS_ID_9911,GWAS_ID_9912,GWAS_ID_9913,GWAS_ID_9914,GWAS_ID_9915,GWAS_ID_9916,GWAS_ID_9917,GWAS_ID_9918,GWAS_ID_9919,GWAS_ID_9920,GWAS_ID_9921,GWAS_ID_9922,GWAS_ID_9923,GWAS_ID_9924,GWAS_ID_9925,GWAS_ID_9926,GWAS_ID_9927,GWAS_ID_9928,GWAS_ID_9929,GWAS_ID_9930,GWAS_ID_9931,GWAS_ID_9932,GWAS_ID_9933,GWAS_ID_9934,GWAS_ID_9935,GWAS_ID_9936,GWAS_ID_9937,GWAS_ID_9938,GWAS_ID_9939,GWAS_ID_9940,GWAS_ID_9941,GWAS_ID_9942,GWAS_ID_9943,GWAS_ID_9944,GWAS_ID_9945,GWAS_ID_9946,GWAS_ID_9947,GWAS_ID_9948,GWAS_ID_9949,GWAS_ID_9950,GWAS_ID_9951,GWAS_ID_9952,GWAS_ID_9953,GWAS_ID_9954,GWAS_ID_9955,GWAS_ID_9956,GWAS_ID_9957,GWAS_ID_9958,GWAS_ID_9959,GWAS_ID_9960,GWAS_ID_9961,GWAS_ID_9962,GWAS_ID_9963,GWAS_ID_9964,GWAS_ID_9965,GWAS_ID_9966,GWAS_ID_9967,GWAS_ID_9968,GWAS_ID_9969,GWAS_ID_9970,GWAS_ID_9971,GWAS_ID_9972,GWAS_ID_9973,GWAS_ID_9974,GWAS_ID_9975,GWAS_ID_9976,GWAS_ID_9977,GWAS_ID_9978,GWAS_ID_9979,GWAS_ID_9980,GWAS_ID_9981,GWAS_ID_9982,GWAS_ID_9983,GWAS_ID_9984,GWAS_ID_9985,GWAS_ID_9986,GWAS_ID_9987,GWAS_ID_9988,GWAS_ID_9989,GWAS_ID_9990,GWAS_ID_9991,GWAS_ID_9992,GWAS_ID_9993,GWAS_ID_9994,GWAS_ID_9995,GWAS_ID_9996,GWAS_ID_9997,GWAS_ID_9998,GWAS_ID_9999,GWAS_ID_10000,GWAS_ID_10001,GWAS_ID_10002,GWAS_ID_10003,GWAS_ID_10004,GWAS_ID_10005,GWAS_ID_10006,GWAS_ID_10007,GWAS_ID_10008 82571 RMVar_ID_82571 Human_SNP_ID_96257188 m1A Human chr2 + 148020703 148020703 148020703 TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGACTTCACCTGCCGCTGCGGACCGTACACAACCA TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGTCTTCACCTGCCGCTGCGGACCGTACACAACCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:148020670..148021604 26863196 MeRIP-seq:(Medium) rs897172 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_425,Clinvar_Rec_3738 GWAS_ID_9628,GWAS_ID_9629,GWAS_ID_9630,GWAS_ID_9631,GWAS_ID_9632,GWAS_ID_9633,GWAS_ID_9634,GWAS_ID_9635,GWAS_ID_9636,GWAS_ID_9637,GWAS_ID_9638,GWAS_ID_9639,GWAS_ID_9640,GWAS_ID_9641,GWAS_ID_9642,GWAS_ID_9643,GWAS_ID_9644,GWAS_ID_9645,GWAS_ID_9646,GWAS_ID_9647,GWAS_ID_9648,GWAS_ID_9649,GWAS_ID_9650,GWAS_ID_9651,GWAS_ID_9652,GWAS_ID_9653,GWAS_ID_9654,GWAS_ID_9655,GWAS_ID_9656,GWAS_ID_9657,GWAS_ID_9658,GWAS_ID_9659,GWAS_ID_9660,GWAS_ID_9661,GWAS_ID_9662,GWAS_ID_9663,GWAS_ID_9664,GWAS_ID_9665,GWAS_ID_9666,GWAS_ID_9667,GWAS_ID_9668,GWAS_ID_9669,GWAS_ID_9670,GWAS_ID_9671,GWAS_ID_9672,GWAS_ID_9673,GWAS_ID_9674,GWAS_ID_9675,GWAS_ID_9676,GWAS_ID_9677,GWAS_ID_9678,GWAS_ID_9679,GWAS_ID_9680,GWAS_ID_9681,GWAS_ID_9682,GWAS_ID_9683,GWAS_ID_9684,GWAS_ID_9685,GWAS_ID_9686,GWAS_ID_9687,GWAS_ID_9688,GWAS_ID_9689,GWAS_ID_9690,GWAS_ID_9691,GWAS_ID_9692,GWAS_ID_9693,GWAS_ID_9694,GWAS_ID_9695,GWAS_ID_9696,GWAS_ID_9697,GWAS_ID_9698,GWAS_ID_9699,GWAS_ID_9700,GWAS_ID_9701,GWAS_ID_9702,GWAS_ID_9703,GWAS_ID_9704,GWAS_ID_9705,GWAS_ID_9706,GWAS_ID_9707,GWAS_ID_9708,GWAS_ID_9709,GWAS_ID_9710,GWAS_ID_9711,GWAS_ID_9712,GWAS_ID_9713,GWAS_ID_9714,GWAS_ID_9715,GWAS_ID_9716,GWAS_ID_9717,GWAS_ID_9718,GWAS_ID_9719,GWAS_ID_9720,GWAS_ID_9721,GWAS_ID_9722,GWAS_ID_9723,GWAS_ID_9724,GWAS_ID_9725,GWAS_ID_9726,GWAS_ID_9727,GWAS_ID_9728,GWAS_ID_9729,GWAS_ID_9730,GWAS_ID_9731,GWAS_ID_9732,GWAS_ID_9733,GWAS_ID_9734,GWAS_ID_9735,GWAS_ID_9736,GWAS_ID_9737,GWAS_ID_9738,GWAS_ID_9739,GWAS_ID_9740,GWAS_ID_9741,GWAS_ID_9742,GWAS_ID_9743,GWAS_ID_9744,GWAS_ID_9745,GWAS_ID_9746,GWAS_ID_9747,GWAS_ID_9748,GWAS_ID_9749,GWAS_ID_9750,GWAS_ID_9751,GWAS_ID_9752,GWAS_ID_9753,GWAS_ID_9754,GWAS_ID_9755,GWAS_ID_9756,GWAS_ID_9757,GWAS_ID_9758,GWAS_ID_9759,GWAS_ID_9760,GWAS_ID_9761,GWAS_ID_9762,GWAS_ID_9763,GWAS_ID_9764,GWAS_ID_9765,GWAS_ID_9766,GWAS_ID_9767,GWAS_ID_9768,GWAS_ID_9769,GWAS_ID_9770,GWAS_ID_9771,GWAS_ID_9772,GWAS_ID_9773,GWAS_ID_9774,GWAS_ID_9775,GWAS_ID_9776,GWAS_ID_9777,GWAS_ID_9778,GWAS_ID_9779,GWAS_ID_9780,GWAS_ID_9781,GWAS_ID_9782,GWAS_ID_9783,GWAS_ID_9784,GWAS_ID_9785,GWAS_ID_9786,GWAS_ID_9787,GWAS_ID_9788,GWAS_ID_9789,GWAS_ID_9790,GWAS_ID_9791,GWAS_ID_9792,GWAS_ID_9793,GWAS_ID_9794,GWAS_ID_9795,GWAS_ID_9796,GWAS_ID_9797,GWAS_ID_9798,GWAS_ID_9799,GWAS_ID_9800,GWAS_ID_9801,GWAS_ID_9802,GWAS_ID_9803,GWAS_ID_9804,GWAS_ID_9805,GWAS_ID_9806,GWAS_ID_9807,GWAS_ID_9808,GWAS_ID_9809,GWAS_ID_9810,GWAS_ID_9811,GWAS_ID_9812,GWAS_ID_9813,GWAS_ID_9814,GWAS_ID_9815,GWAS_ID_9816,GWAS_ID_9817,GWAS_ID_9818,GWAS_ID_9819,GWAS_ID_9820,GWAS_ID_9821,GWAS_ID_9822,GWAS_ID_9823,GWAS_ID_9824,GWAS_ID_9825,GWAS_ID_9826,GWAS_ID_9827,GWAS_ID_9828,GWAS_ID_9829,GWAS_ID_9830,GWAS_ID_9831,GWAS_ID_9832,GWAS_ID_9833,GWAS_ID_9834,GWAS_ID_9835,GWAS_ID_9836,GWAS_ID_9837,GWAS_ID_9838,GWAS_ID_9839,GWAS_ID_9840,GWAS_ID_9841,GWAS_ID_9842,GWAS_ID_9843,GWAS_ID_9844,GWAS_ID_9845,GWAS_ID_9846,GWAS_ID_9847,GWAS_ID_9848,GWAS_ID_9849,GWAS_ID_9850,GWAS_ID_9851,GWAS_ID_9852,GWAS_ID_9853,GWAS_ID_9854,GWAS_ID_9855,GWAS_ID_9856,GWAS_ID_9857,GWAS_ID_9858,GWAS_ID_9859,GWAS_ID_9860,GWAS_ID_9861,GWAS_ID_9862,GWAS_ID_9863,GWAS_ID_9864,GWAS_ID_9865,GWAS_ID_9866,GWAS_ID_9867,GWAS_ID_9868,GWAS_ID_9869,GWAS_ID_9870,GWAS_ID_9871,GWAS_ID_9872,GWAS_ID_9873,GWAS_ID_9874,GWAS_ID_9875,GWAS_ID_9876,GWAS_ID_9877,GWAS_ID_9878,GWAS_ID_9879,GWAS_ID_9880,GWAS_ID_9881,GWAS_ID_9882,GWAS_ID_9883,GWAS_ID_9884,GWAS_ID_9885,GWAS_ID_9886,GWAS_ID_9887,GWAS_ID_9888,GWAS_ID_9889,GWAS_ID_9890,GWAS_ID_9891,GWAS_ID_9892,GWAS_ID_9893,GWAS_ID_9894,GWAS_ID_9895,GWAS_ID_9896,GWAS_ID_9897,GWAS_ID_9898,GWAS_ID_9899,GWAS_ID_9900,GWAS_ID_9901,GWAS_ID_9902,GWAS_ID_9903,GWAS_ID_9904,GWAS_ID_9905,GWAS_ID_9906,GWAS_ID_9907,GWAS_ID_9908,GWAS_ID_9909,GWAS_ID_9910,GWAS_ID_9911,GWAS_ID_9912,GWAS_ID_9913,GWAS_ID_9914,GWAS_ID_9915,GWAS_ID_9916,GWAS_ID_9917,GWAS_ID_9918,GWAS_ID_9919,GWAS_ID_9920,GWAS_ID_9921,GWAS_ID_9922,GWAS_ID_9923,GWAS_ID_9924,GWAS_ID_9925,GWAS_ID_9926,GWAS_ID_9927,GWAS_ID_9928,GWAS_ID_9929,GWAS_ID_9930,GWAS_ID_9931,GWAS_ID_9932,GWAS_ID_9933,GWAS_ID_9934,GWAS_ID_9935,GWAS_ID_9936,GWAS_ID_9937,GWAS_ID_9938,GWAS_ID_9939,GWAS_ID_9940,GWAS_ID_9941,GWAS_ID_9942,GWAS_ID_9943,GWAS_ID_9944,GWAS_ID_9945,GWAS_ID_9946,GWAS_ID_9947,GWAS_ID_9948,GWAS_ID_9949,GWAS_ID_9950,GWAS_ID_9951,GWAS_ID_9952,GWAS_ID_9953,GWAS_ID_9954,GWAS_ID_9955,GWAS_ID_9956,GWAS_ID_9957,GWAS_ID_9958,GWAS_ID_9959,GWAS_ID_9960,GWAS_ID_9961,GWAS_ID_9962,GWAS_ID_9963,GWAS_ID_9964,GWAS_ID_9965,GWAS_ID_9966,GWAS_ID_9967,GWAS_ID_9968,GWAS_ID_9969,GWAS_ID_9970,GWAS_ID_9971,GWAS_ID_9972,GWAS_ID_9973,GWAS_ID_9974,GWAS_ID_9975,GWAS_ID_9976,GWAS_ID_9977,GWAS_ID_9978,GWAS_ID_9979,GWAS_ID_9980,GWAS_ID_9981,GWAS_ID_9982,GWAS_ID_9983,GWAS_ID_9984,GWAS_ID_9985,GWAS_ID_9986,GWAS_ID_9987,GWAS_ID_9988,GWAS_ID_9989,GWAS_ID_9990,GWAS_ID_9991,GWAS_ID_9992,GWAS_ID_9993,GWAS_ID_9994,GWAS_ID_9995,GWAS_ID_9996,GWAS_ID_9997,GWAS_ID_9998,GWAS_ID_9999,GWAS_ID_10000,GWAS_ID_10001,GWAS_ID_10002,GWAS_ID_10003,GWAS_ID_10004,GWAS_ID_10005,GWAS_ID_10006,GWAS_ID_10007,GWAS_ID_10008 82572 RMVar_ID_82572 Human_SNP_ID_96257363 m1A Human chr2 + 148021148 148021147 148021148 GCAGCTGATGATGAAGAGAGAGGCAGTGGCAGAGGGGGGGCACCTTTTATTTCTATTTTTAAAGG GCAGCTGATGATGAAGAGAGAGGCAGTGGCAG_GGGGGGGCACCTTTTATTTCTATTTTTAAAGG GA G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:148021102..148021212 26863196 MeRIP-seq:(Medium) rs1266890970 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25469228 82573 RMVar_ID_82573 Human_SNP_ID_96257365 m1A Human chr2 + 148021148 148021148 148021148 GCAGCTGATGATGAAGAGAGAGGCAGTGGCAGAGGGGGGGCACCTTTTATTTCTATTTTTAAAGG GCAGCTGATGATGAAGAGAGAGGCAGTGGCAGCGGGGGGGCACCTTTTATTTCTATTTTTAAAGG A C MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:148021102..148021212 26863196 MeRIP-seq:(Medium) rs1288587772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25469228 82574 RMVar_ID_82574 Human_SNP_ID_96257449 m1A Human chr2 + 148021418 148021418 148021418 TCCTCCTCTTTGGCCGTGAGAGGAGGAGAGAAAGAAACCAAAAGCCTCTTAGCAACACAGACCCT TCCTCCTCTTTGGCCGTGAGAGGAGGAGAGAAGGAAACCAAAAGCCTCTTAGCAACACAGACCCT A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:148021367..148021616 26863196 MeRIP-seq:(Medium) rs1284878025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18949581 82575 RMVar_ID_82575 Human_SNP_ID_96263265 m1A Human chr2 + 148046993 148046993 148046993 CCCCTTATGATGTCTTTCATCGCAGCTAACCAACCCACTTCCTCTTCAAGATTATGTTGTGCTCC CCCCTTATGATGTCTTTCATCGCAGCTAACCAGCCCACTTCCTCTTCAAGATTATGTTGTGCTCC A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:148046962..148047088 26863196 MeRIP-seq:(Medium) rs1423947068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1375592,Human_RBP_ID_6833349 RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763 82576 RMVar_ID_82576 Human_SNP_ID_96404649 m1A Human chr2 + 148644801 148644801 148644801 GGCCATGGCGCAGGGAGCGGATCGGGCGGGCGAGCGGCGGATCTAGTGTGTGGAGGCGGCCGCGG GGCCATGGCGCAGGGAGCGGATCGGGCGGGCGGGCGGCGGATCTAGTGTGTGGAGGCGGCCGCGG A G EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:148644751..148645003 26863196 MeRIP-seq:(Medium) rs1212754012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623653,Human_RBP_ID_5470063,Human_RBP_ID_6834056,Human_RBP_ID_18421905,Human_RBP_ID_27840111 82577 RMVar_ID_82577 Human_SNP_ID_96404653 m1A Human chr2 + 148644809 148644809 148644809 CGCAGGGAGCGGATCGGGCGGGCGAGCGGCGGATCTAGTGTGTGGAGGCGGCCGCGGGCGCGGGG CGCAGGGAGCGGATCGGGCGGGCGAGCGGCGGCTCTAGTGTGTGGAGGCGGCCGCGGGCGCGGGG A C EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:148644742..148644934 26863196 MeRIP-seq:(Medium) rs991944853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4583025,Human_RBP_ID_6834056,Human_RBP_ID_18421905,Human_RBP_ID_27840111 82578 RMVar_ID_82578 Human_SNP_ID_96404654 m1A Human chr2 + 148644809 148644809 148644809 CGCAGGGAGCGGATCGGGCGGGCGAGCGGCGGATCTAGTGTGTGGAGGCGGCCGCGGGCGCGGGG CGCAGGGAGCGGATCGGGCGGGCGAGCGGCGGGTCTAGTGTGTGGAGGCGGCCGCGGGCGCGGGG A G EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:148644742..148644934 26863196 MeRIP-seq:(Medium) rs991944853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4583025,Human_RBP_ID_6834056,Human_RBP_ID_18421905,Human_RBP_ID_27840111 82579 RMVar_ID_82579 Human_SNP_ID_96404662 m1A Human chr2 - 148644849 148644830 148644850 CCGGCCACAGCATGGGCGCCCACCCCGCCCGAAAACAGCCCCCCGCGCCCGCGGCCGCCTCCACA CCGGCCACAGCATGGGCGCCCACCCCGCCCG____________________CGGCCGCCTCCACA GCGGGCGCGGGGGGCTGTTTT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:148644800..148645047 26863196 MeRIP-seq:(Medium) rs1215473186 Functional Loss DEL dbSNP153 32..51 33 - - - 82580 RMVar_ID_82580 Human_SNP_ID_96628346 m1A Human chr2 - 149587720 149587720 149587720 TAGGTGCTACCACCGCTGCCGTCGCCGCCGCCATTTTGATGGCAGGAAGAGTCCGGTTCTGGGAC TAGGTGCTACCACCGCTGCCGTCGCCGCCGCCGTTTTGATGGCAGGAAGAGTCCGGTTCTGGGAC T C MMADHC Ensembl:ENSG00000168288 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:149587487..149587731 26863196 MeRIP-seq:(Medium) rs1457045383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_535478,Human_RBP_ID_4623660,Human_RBP_ID_9330690,Human_RBP_ID_17392805,Human_RBP_ID_23829394,Human_RBP_ID_26818976 Human_Splice_Rec_304953,Human_Splice_Rec_304979,Human_Splice_Rec_304995 RMVar_hsa_circ_90768,RMVar_hsa_circ_203789 82581 RMVar_ID_82581 Human_SNP_ID_345010891 m1A Human chr7 + 150323511 150323511 150323511 GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGACTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGCCTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG A C ZBED6CL,LRRC61 Ensembl:ENSG00000188707,Ensembl:ENSG00000127399 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:150323241..150323550;chr7:150323251..150323550 26863196 MeRIP-seq:(Medium) rs967329899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955073,Human_RBP_ID_4956032,Human_RBP_ID_5153449,Human_RBP_ID_9338045,Human_RBP_ID_18426119,Human_RBP_ID_19020252,Human_RBP_ID_22111367,Human_RBP_ID_22463816,Human_RBP_ID_27353570 Human_Splice_Rec_936631,Human_Splice_Rec_936635,Human_Splice_Rec_936637,Human_Splice_Rec_936643 Human_miRNA_ID_2155574,Human_miRNA_ID_2159136 RMVar_hsa_circ_81007,RMVar_hsa_circ_88109,RMVar_hsa_circ_249391,RMVar_hsa_circ_249392 82582 RMVar_ID_82582 Human_SNP_ID_345010892 m1A Human chr7 + 150323511 150323511 150323511 GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGACTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGGCTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG A G ZBED6CL,LRRC61 Ensembl:ENSG00000188707,Ensembl:ENSG00000127399 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:150323241..150323550;chr7:150323251..150323550 26863196 MeRIP-seq:(Medium) rs967329899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955073,Human_RBP_ID_4956032,Human_RBP_ID_5153449,Human_RBP_ID_9338045,Human_RBP_ID_18426119,Human_RBP_ID_19020252,Human_RBP_ID_22111367,Human_RBP_ID_22463816,Human_RBP_ID_27353570 Human_Splice_Rec_936631,Human_Splice_Rec_936635,Human_Splice_Rec_936637,Human_Splice_Rec_936643 Human_miRNA_ID_2155574,Human_miRNA_ID_2159136 RMVar_hsa_circ_81007,RMVar_hsa_circ_88109,RMVar_hsa_circ_249391,RMVar_hsa_circ_249392 82583 RMVar_ID_82583 Human_SNP_ID_345010893 m1A Human chr7 + 150323511 150323511 150323511 GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGACTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG GGCGCCGGCTCTGCGGTGCGGAGTTGCGCCGGTCTTCCCAGCTTGGCCAGTGGCTCCGCAGGCTG A T ZBED6CL,LRRC61 Ensembl:ENSG00000188707,Ensembl:ENSG00000127399 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:150323241..150323550;chr7:150323251..150323550 26863196 MeRIP-seq:(Medium) rs967329899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955073,Human_RBP_ID_4956032,Human_RBP_ID_5153449,Human_RBP_ID_9338045,Human_RBP_ID_18426119,Human_RBP_ID_19020252,Human_RBP_ID_22111367,Human_RBP_ID_22463816,Human_RBP_ID_27353570 Human_Splice_Rec_936631,Human_Splice_Rec_936635,Human_Splice_Rec_936637,Human_Splice_Rec_936643 Human_miRNA_ID_2155574,Human_miRNA_ID_2159136 RMVar_hsa_circ_81007,RMVar_hsa_circ_88109,RMVar_hsa_circ_249391,RMVar_hsa_circ_249392 82584 RMVar_ID_82584 Human_SNP_ID_345014282 m1A Human chr7 - 150336825 150336825 150336825 TGGAAGTCGGTTGGGATGGCCTGGGCCCTGGCAGGACTGTCACAGGGTTCCACTGGGGGTCAGCT TGGAAGTCGGTTGGGATGGCCTGGGCCCTGGCCGGACTGTCACAGGGTTCCACTGGGGGTCAGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150336777..150336844 26863196 MeRIP-seq:(Medium) rs1254880272 Functional Loss SNV dbSNP153 33..33 33 - - - 82585 RMVar_ID_82585 Human_SNP_ID_345015505 m1A Human chr7 + 150340084 150340082 150340084 GCACTCACACCCAGCATGCGCCCATTGCTCTCACACCCCTTCACTCACCCCATTGGGCCTGACTT GCACTCACACCCAGCATGCGCCCATTGCTCT__CACCCCTTCACTCACCCCATTGGGCCTGACTT TCA T AC005586.2 Ensembl:ENSG00000261305 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150340076..150340171 26863196 MeRIP-seq:(Medium) rs760297682 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18095486,Human_RBP_ID_22424366 82586 RMVar_ID_82586 Human_SNP_ID_345017164 m1A Human chr7 + 150346694 150346694 150346694 TCTGCATGCAGATCGAGATCAGAGCAGAGATGAGACTGGGGATTGGAGAAGGAAGTAGCTTGCCC TCTGCATGCAGATCGAGATCAGAGCAGAGATGGGACTGGGGATTGGAGAAGGAAGTAGCTTGCCC A G lnc-LRRC61-2,lnc-LRRC61-2:2,RF00017-4544,lnc-LRRC61-2:3,lnc-LRRC61-2:4 RNACentral:URS00008B8B85,RNACentral:URS00008B8E4E,RNACentral:URS000093B8FA,RNACentral:URS00008B2747,RNACentral:URS00008BDFEF lincRNA,lincRNA,SRP RNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:150346522..150347015 26863196 MeRIP-seq:(Medium) rs546174202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7711745,Human_RBP_ID_16067185 82587 RMVar_ID_82587 Human_SNP_ID_345024414 m1A Human chr7 + 150372926 150372926 150372926 CTTCGACGACGAGGAGAGACTCCTGGCCCACCAGAAGAAGCACGATGTCTGAGACGGTGGGCGGG CTTCGACGACGAGGAGAGACTCCTGGCCCACCGGAAGAAGCACGATGTCTGAGACGGTGGGCGGG A G ZNF775,REPIN1 Ensembl:ENSG00000196456,Ensembl:ENSG00000214022 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:150372876..150373175 26863196 MeRIP-seq:(Medium) rs1287170665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1683495,Human_RBP_ID_2037613,Human_RBP_ID_9311618,Human_RBP_ID_16067223,Human_RBP_ID_27353695 82588 RMVar_ID_82588 Human_SNP_ID_345024570 m1A Human chr7 + 150373609 150373609 150373609 CAAGGCATTTACTCCTTGGTCTGTCTCGCTTTATCTGTCGCCCCTCCCAGCGCTGAGAGCCTCCC CAAGGCATTTACTCCTTGGTCTGTCTCGCTTTCTCTGTCGCCCCTCCCAGCGCTGAGAGCCTCCC A C ZNF775,REPIN1 Ensembl:ENSG00000196456,Ensembl:ENSG00000214022 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:150373451..150373700 26863196 MeRIP-seq:(Medium) rs184568102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678712,Human_RBP_ID_3071170,Human_RBP_ID_16067237,Human_RBP_ID_18196144,Human_RBP_ID_18960523,Human_RBP_ID_21560409,Human_RBP_ID_21904252,Human_RBP_ID_24515487,Human_RBP_ID_27107767,Human_RBP_ID_27529590 Human_miRNA_ID_298956,Human_miRNA_ID_1781172 82589 RMVar_ID_82589 Human_SNP_ID_345024571 m1A Human chr7 + 150373609 150373609 150373609 CAAGGCATTTACTCCTTGGTCTGTCTCGCTTTATCTGTCGCCCCTCCCAGCGCTGAGAGCCTCCC CAAGGCATTTACTCCTTGGTCTGTCTCGCTTTGTCTGTCGCCCCTCCCAGCGCTGAGAGCCTCCC A G ZNF775,REPIN1 Ensembl:ENSG00000196456,Ensembl:ENSG00000214022 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:150373451..150373700 26863196 MeRIP-seq:(Medium) rs184568102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678712,Human_RBP_ID_3071170,Human_RBP_ID_16067237,Human_RBP_ID_18196144,Human_RBP_ID_18960523,Human_RBP_ID_21560409,Human_RBP_ID_21904252,Human_RBP_ID_24515487,Human_RBP_ID_27107767,Human_RBP_ID_27529590 Human_miRNA_ID_298956,Human_miRNA_ID_1781172 82590 RMVar_ID_82590 Human_SNP_ID_345030543 m1A Human chr7 + 150396584 150396584 150396584 AGCGGCTGCTGCAGACGCTGGCGCCGCAGGCCATGCTTGTGGAGAAGGACAAGGAGAACATATTT AGCGGCTGCTGCAGACGCTGGCGCCGCAGGCCGTGCTTGTGGAGAAGGACAAGGAGAACATATTT A G ZNF775,AC073111.3 Ensembl:ENSG00000196456,Ensembl:ENSG00000284048 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150396486..150396637 26863196 MeRIP-seq:(Medium) rs1360043369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_936758,Human_Splice_Rec_936762,Human_Splice_Rec_936766 82591 RMVar_ID_82591 Human_SNP_ID_345031470 m1A Human chr7 + 150398540 150398540 150398540 GCCAAGACTCGGCGATACCAAGGATGGAAGCCAGAGGCTGTGGCGAGGGAGAGCCAAGCATATTC GCCAAGACTCGGCGATACCAAGGATGGAAGCCGGAGGCTGTGGCGAGGGAGAGCCAAGCATATTC A G ZNF775,AC073111.3 Ensembl:ENSG00000196456,Ensembl:ENSG00000284048 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150398489..150398560 26863196 MeRIP-seq:(Medium) rs574161536 Functional Loss SNV dbSNP153 33..33 33 - - - 82592 RMVar_ID_82592 Human_SNP_ID_345033349 m1A Human chr7 + 150405882 150405882 150405882 CTGTAGAGCAAAGAGCTGCGGCCGGAGACCGGAGGAGCAGGGGCTCAGCTGGGCTGTGAGTGTGG CTGTAGAGCAAAGAGCTGCGGCCGGAGACCGGGGGAGCAGGGGCTCAGCTGGGCTGTGAGTGTGG A G AC073111.4,AC073111.3 Ensembl:ENSG00000284691,Ensembl:ENSG00000284048 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:150405832..150406074 26863196 MeRIP-seq:(Medium) rs1253645060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_936791,Human_Splice_Rec_936793 82593 RMVar_ID_82593 Human_SNP_ID_345033356 m1A Human chr7 - 150405904 150405904 150405904 CCCCAAGTTCTTTCCTCCCATGCCACACTCACAGCCCAGCTGAGCCCCTGCTCCTCCGGTCTCCG CCCCAAGTTCTTTCCTCCCATGCCACACTCACGGCCCAGCTGAGCCCCTGCTCCTCCGGTCTCCG T C lnc-RARRES2-5 RNACentral:URS00008B800F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150405517..150406058 26863196 MeRIP-seq:(Medium) rs1222247251 Functional Loss SNV dbSNP153 33..33 33 - - - 82594 RMVar_ID_82594 Human_SNP_ID_345033470 m1A Human chr7 - 150406375 150406375 150406375 GCATTCCAAAGGGCCACTTCTCCTGTAGATGCACTGTCTACTGCCACCACTCCCACGACCCCCAC GCATTCCAAAGGGCCACTTCTCCTGTAGATGCGCTGTCTACTGCCACCACTCCCACGACCCCCAC T C lnc-RARRES2-5 RNACentral:URS00008B800F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:150406354..150406424 26863196 MeRIP-seq:(Medium) rs190185830 Functional Loss SNV dbSNP153 33..33 33 - - - 82595 RMVar_ID_82595 Human_SNP_ID_345198643 m1A Human chr7 - 151028502 151028502 151028502 GAAATAAATGCACCAGCATGCTGACGCGGTAAAACAGGAGCCGCCGGCAATAGCAGTTTCACCCT GAAATAAATGCACCAGCATGCTGACGCGGTAAGACAGGAGCCGCCGGCAATAGCAGTTTCACCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151028451..151028625 26863196 MeRIP-seq:(Medium) rs769421665 Functional Loss SNV dbSNP153 33..33 33 - - - 82596 RMVar_ID_82596 Human_SNP_ID_345198654 m1A Human chr7 + 151028516 151028516 151028516 ATTGCCGGCGGCTCCTGTTTTACCGCGTCAGCATGCTGGTGCATTTATTTCGGGTCGGGATTCGG ATTGCCGGCGGCTCCTGTTTTACCGCGTCAGCTTGCTGGTGCATTTATTTCGGGTCGGGATTCGG A T ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151028451..151028646 26863196 MeRIP-seq:(Medium) rs1251781553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338076,Human_RBP_ID_22319258 Human_Splice_Rec_937539,Human_Splice_Rec_937567,Human_Splice_Rec_937571,Human_Splice_Rec_937601,Human_Splice_Rec_937631,Human_Splice_Rec_937639,Human_Splice_Rec_937645,Human_Splice_Rec_937647,Human_Splice_Rec_937653,Human_Splice_Rec_937671,Human_Splice_Rec_937703,Human_Splice_Rec_937729,Human_Splice_Rec_937759,Human_Splice_Rec_937777,Human_Splice_Rec_937795,Human_Splice_Rec_937799 82597 RMVar_ID_82597 Human_SNP_ID_345198658 m1A Human chr7 + 151028530 151028526 151028531 CTGTTTTACCGCGTCAGCATGCTGGTGCATTTATTTCGGGTCGGGATTCGGGGTGGCCCATTCCC CTGTTTTACCGCGTCAGCATGCTGGTGCA_____TTCGGGTCGGGATTCGGGGTGGCCCATTCCC ATTTAT A ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151028480..151028638 26863196 MeRIP-seq:(Medium) rs1318765892 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_4961224,Human_RBP_ID_7711832,Human_RBP_ID_9338076,Human_RBP_ID_22319258,Human_RBP_ID_22426661 Human_Splice_Rec_937539,Human_Splice_Rec_937567,Human_Splice_Rec_937571,Human_Splice_Rec_937601,Human_Splice_Rec_937631,Human_Splice_Rec_937639,Human_Splice_Rec_937645,Human_Splice_Rec_937647,Human_Splice_Rec_937653,Human_Splice_Rec_937671,Human_Splice_Rec_937703,Human_Splice_Rec_937729,Human_Splice_Rec_937759,Human_Splice_Rec_937777,Human_Splice_Rec_937795,Human_Splice_Rec_937799 82598 RMVar_ID_82598 Human_SNP_ID_345198677 m1A Human chr7 + 151028557 151028557 151028557 CATTTATTTCGGGTCGGGATTCGGGGTGGCCCATTCCCAGGCAGGCTGCTACCGCCCCTCCGCTT CATTTATTTCGGGTCGGGATTCGGGGTGGCCCGTTCCCAGGCAGGCTGCTACCGCCCCTCCGCTT A G ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151028451..151028669 26863196 MeRIP-seq:(Medium) rs771464302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254559,Human_RBP_ID_794562,Human_RBP_ID_18451318,Human_RBP_ID_22426661 Human_Splice_Rec_937539,Human_Splice_Rec_937567,Human_Splice_Rec_937571,Human_Splice_Rec_937601,Human_Splice_Rec_937631,Human_Splice_Rec_937639,Human_Splice_Rec_937645,Human_Splice_Rec_937647,Human_Splice_Rec_937653,Human_Splice_Rec_937671,Human_Splice_Rec_937703,Human_Splice_Rec_937729,Human_Splice_Rec_937759,Human_Splice_Rec_937777,Human_Splice_Rec_937795,Human_Splice_Rec_937799 82599 RMVar_ID_82599 Human_SNP_ID_345200175 m1A Human chr7 + 151033624 151033624 151033624 TCTCTCCTTACAGGTACTCTGATGGCTACCGCAGCTCCTCCCTCCTCCGGGCCGTGGCCCACCTG TCTCTCCTTACAGGTACTCTGATGGCTACCGCCGCTCCTCCCTCCTCCGGGCCGTGGCCCACCTG A C ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151033608..151033765 26863196 MeRIP-seq:(Medium) rs1177779767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8661849,Human_RBP_ID_27842987 Human_Splice_Rec_937570,Human_Splice_Rec_937572,Human_Splice_Rec_937630,Human_Splice_Rec_937634,Human_Splice_Rec_937674,Human_Splice_Rec_937730,Human_Splice_Rec_937760,Human_Splice_Rec_937778,Human_Splice_Rec_937798,Human_Splice_Rec_937810 RMVar_hsa_circ_35689 82600 RMVar_ID_82600 Human_SNP_ID_345200191 m1A Human chr7 + 151033652 151033652 151033652 CCGCAGCTCCTCCCTCCTCCGGGCCGTGGCCCACCTGCGGTCCCAGCTCTGGGCCCACCTCCCTC CCGCAGCTCCTCCCTCCTCCGGGCCGTGGCCCCCCTGCGGTCCCAGCTCTGGGCCCACCTCCCTC A C ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:151033526..151033825 26863196 MeRIP-seq:(Medium) rs756294991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27842987 Human_Splice_Rec_937570,Human_Splice_Rec_937572,Human_Splice_Rec_937630,Human_Splice_Rec_937634,Human_Splice_Rec_937674,Human_Splice_Rec_937730,Human_Splice_Rec_937760,Human_Splice_Rec_937778,Human_Splice_Rec_937798,Human_Splice_Rec_937810 RMVar_hsa_circ_35689 82601 RMVar_ID_82601 Human_SNP_ID_345200192 m1A Human chr7 + 151033652 151033652 151033652 CCGCAGCTCCTCCCTCCTCCGGGCCGTGGCCCACCTGCGGTCCCAGCTCTGGGCCCACCTCCCTC CCGCAGCTCCTCCCTCCTCCGGGCCGTGGCCCGCCTGCGGTCCCAGCTCTGGGCCCACCTCCCTC A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:151033526..151033825 26863196 MeRIP-seq:(Medium) rs756294991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27842987 Human_Splice_Rec_937570,Human_Splice_Rec_937572,Human_Splice_Rec_937630,Human_Splice_Rec_937634,Human_Splice_Rec_937674,Human_Splice_Rec_937730,Human_Splice_Rec_937760,Human_Splice_Rec_937778,Human_Splice_Rec_937798,Human_Splice_Rec_937810 RMVar_hsa_circ_35689 82602 RMVar_ID_82602 Human_SNP_ID_345200214 m1A Human chr7 - 151033694 151033694 151033694 AGCACCAGGCAGAGGGGCTCCATCTGGGAGCTAGGGGGGCTCGAGGGAGGTGGGCCCAGAGCTGG AGCACCAGGCAGAGGGGCTCCATCTGGGAGCTTGGGGGGCTCGAGGGAGGTGGGCCCAGAGCTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151033544..151033775 26863196 MeRIP-seq:(Medium) rs1457359666 Functional Loss SNV dbSNP153 33..33 33 - - - 82603 RMVar_ID_82603 Human_SNP_ID_345200873 m1A Human chr7 - 151035618 151035618 151035618 GCGTGAGGCGTGTCGACAGCATGGACAGGGACACCAGGCAGCCTGCCACCTGGGTGCAGCTTCGC GCGTGAGGCGTGTCGACAGCATGGACAGGGACGCCAGGCAGCCTGCCACCTGGGTGCAGCTTCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:151034816..151035768 32194978 MeRIP-seq:(Medium) rs1433820566 Functional Loss SNV dbSNP153 33..33 33 - - - 82604 RMVar_ID_82604 Human_SNP_ID_345200933 m1A Human chr7 + 151035741 151035741 151035741 CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCAGGTACCGGCATTCCTGGCCATCCTCTTCACCC CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCCGGTACCGGCATTCCTGGCCATCCTCTTCACCC A C ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:151035707..151035790;chr7:151035712..151035785 26863196 MeRIP-seq:(Medium) rs137922285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19137633 Human_Splice_Rec_937547,Human_Splice_Rec_937581,Human_Splice_Rec_937609,Human_Splice_Rec_937683,Human_Splice_Rec_937709,Human_Splice_Rec_937739,Human_Splice_Rec_937769,Human_Splice_Rec_937787,Human_Splice_Rec_937815 RMVar_hsa_circ_11538,RMVar_hsa_circ_60337 82605 RMVar_ID_82605 Human_SNP_ID_345201029 m1A Human chr7 + 151035948 151035948 151035948 TGGGCAATGTGCGGACTGTGCGTGCCTTCGCCATGGAGCAACGGGAAGAGGAGTGAGTCCTGGGA TGGGCAATGTGCGGACTGTGCGTGCCTTCGCCGTGGAGCAACGGGAAGAGGAGTGAGTCCTGGGA A G ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151035901..151035975 26863196 MeRIP-seq:(Medium) rs770720559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021617 Human_Splice_Rec_937548,Human_Splice_Rec_937549,Human_Splice_Rec_937582,Human_Splice_Rec_937583,Human_Splice_Rec_937610,Human_Splice_Rec_937611,Human_Splice_Rec_937684,Human_Splice_Rec_937685,Human_Splice_Rec_937710,Human_Splice_Rec_937711,Human_Splice_Rec_937740,Human_Splice_Rec_937741,Human_Splice_Rec_937770,Human_Splice_Rec_937771,Human_Splice_Rec_937788,Human_Splice_Rec_937789,Human_Splice_Rec_937816,Human_Splice_Rec_937817 RMVar_hsa_circ_11538,RMVar_hsa_circ_60337 82606 RMVar_ID_82606 Human_SNP_ID_345203456 m1A Human chr7 + 151043504 151043504 151043504 GGTGGAGGGTCAGAGACAGGACTAGGGTGCACAGTGTGGGGTGGAGGGTCAGAGACAGGACTAGG GGTGGAGGGTCAGAGACAGGACTAGGGTGCACGGTGTGGGGTGGAGGGTCAGAGACAGGACTAGG A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151043500..151043682 26863196 MeRIP-seq:(Medium) rs1211206102 Functional Loss SNV dbSNP153 33..33 33 - - - 82607 RMVar_ID_82607 Human_SNP_ID_345204995 m1A Human chr7 - 151048774 151048772 151048775 AGATAGGATTCAGGAGGCCAGGCAAGGAGAGGAGAAGAGAGGGTGGGAGACAGCCAAGGTTGGAA AGATAGGATTCAGGAGGCCAGGCAAGGAGAG___AAGAGAGGGTGGGAGACAGCCAAGGTTGGAA TCTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:151048663..151048789 26863196 MeRIP-seq:(Medium) rs558495765 Functional Loss DEL dbSNP153 32..34 33 - - - 82608 RMVar_ID_82608 Human_SNP_ID_345206725 m1A Human chr7 - 151052636 151052636 151052636 GACACAGACAGCAGGTCTAGAGCTGTGTGACAAGGTAGCAGGTGCGGTGGGAGGCGGAGAGAGTC GACACAGACAGCAGGTCTAGAGCTGTGTGACACGGTAGCAGGTGCGGTGGGAGGCGGAGAGAGTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151052545..151052672 26863196 MeRIP-seq:(Medium) rs759146789 Functional Loss SNV dbSNP153 33..33 33 - - - 82609 RMVar_ID_82609 Human_SNP_ID_345206757 m1A Human chr7 - 151052702 151052702 151052702 TGGGGTGAAGACGGAAAAGCTACGTGCAGGCTAGGCATGTCCAGGATGTCAGGGCGGGGCTCCGA TGGGGTGAAGACGGAAAAGCTACGTGCAGGCTGGGCATGTCCAGGATGTCAGGGCGGGGCTCCGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151052534..151052720 26863196 MeRIP-seq:(Medium) rs1483322397 Functional Loss SNV dbSNP153 33..33 33 - - - 82610 RMVar_ID_82610 Human_SNP_ID_345206758 m1A Human chr7 + 151052703 151052703 151052703 CGGAGCCCCGCCCTGACATCCTGGACATGCCTAGCCTGCACGTAGCTTTTCCGTCTTCACCCCAA CGGAGCCCCGCCCTGACATCCTGGACATGCCTTGCCTGCACGTAGCTTTTCCGTCTTCACCCCAA A T ASIC3 Ensembl:ENSG00000213199 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151052478..151052718 26863196 MeRIP-seq:(Medium) rs1308792381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678799 Human_Splice_Rec_937942,Human_Splice_Rec_937952 82611 RMVar_ID_82611 Human_SNP_ID_345207185 m1A Human chr7 + 151054265 151054265 151054265 GGCATTGAGTTTGGGCACGACGTTCACCAGGGATGTTGTGGCCGGGTACATCGGATAGGGCTGTG GGCATTGAGTTTGGGCACGACGTTCACCAGGGGTGTTGTGGCCGGGTACATCGGATAGGGCTGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:151054060..151054276 32194978 MeRIP-seq:(Medium) rs998206886 Functional Loss SNV dbSNP153 33..33 33 - - - 82612 RMVar_ID_82612 Human_SNP_ID_345207327 m1A Human chr7 - 151054686 151054686 151054686 CAGGGCAAGGACTGTTTCATTAGGACTAGGACAGCAGCATGTGGGTTAGGTGATTGTCATGGGAA CAGGGCAAGGACTGTTTCATTAGGACTAGGACGGCAGCATGTGGGTTAGGTGATTGTCATGGGAA T C CDK5 Ensembl:ENSG00000164885 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151054684..151054749 26863196 MeRIP-seq:(Medium) rs866868472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3071217 RMVar_hsa_circ_249411,RMVar_hsa_circ_98196,RMVar_hsa_circ_121476,RMVar_hsa_circ_90779,RMVar_hsa_circ_249412,RMVar_hsa_circ_53519,RMVar_hsa_circ_249410,RMVar_hsa_circ_94759,RMVar_hsa_circ_249414 82613 RMVar_ID_82613 Human_SNP_ID_345207371 m1A Human chr7 - 151054854 151054854 151054854 AGGGGTGCTGGACACCCTGATTGTCACAGTGCAAATGCACACTGGAGAAGGTGTGGCTTGGAGAC AGGGGTGCTGGACACCCTGATTGTCACAGTGCGAATGCACACTGGAGAAGGTGTGGCTTGGAGAC T C CDK5 Ensembl:ENSG00000164885 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151054852..151054938 26863196 MeRIP-seq:(Medium) rs1233290263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249411,RMVar_hsa_circ_98196,RMVar_hsa_circ_121476,RMVar_hsa_circ_90779,RMVar_hsa_circ_249412,RMVar_hsa_circ_53519,RMVar_hsa_circ_249410,RMVar_hsa_circ_94759,RMVar_hsa_circ_249414 82614 RMVar_ID_82614 Human_SNP_ID_345208308 m1A Human chr7 - 151057870 151057870 151057870 CCGGGGCCAGAGTCTTAAAACCGAGGGCCCGCAGGGGTCCCCGCGGCCGCCGCGATGCAGAAATA CCGGGGCCAGAGTCTTAAAACCGAGGGCCCGCGGGGGTCCCCGCGGCCGCCGCGATGCAGAAATA T C CDK5 Ensembl:ENSG00000164885 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:151057773..151057900;chr7:151057775..151057884;chr7:151057771..151057882;chr7:151057788..151057872 26863196 MeRIP-seq:(Medium) rs775513156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678807,Human_RBP_ID_4930889 Human_Splice_Rec_937959,Human_Splice_Rec_937979,Human_Splice_Rec_938013 82615 RMVar_ID_82615 Human_SNP_ID_345208834 m1A Human chr7 + 151059754 151059754 151059754 AGACCCCGAGACCCCCGGGGCACGAAGTCCAGAGCGAGCGGGTAGGCGGAGAGGTGGTGGCGGGG AGACCCCGAGACCCCCGGGGCACGAAGTCCAGGGCGAGCGGGTAGGCGGAGAGGTGGTGGCGGGG A G SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:151059601..151059818;chr7:151059576..151059807;chr7:151059576..151059833;chr7:151059601..151059823 26863196 MeRIP-seq:(Medium) rs910355144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956048,Human_RBP_ID_8944214,Human_RBP_ID_9312068,Human_RBP_ID_18426462,Human_RBP_ID_26772279 Human_Splice_Rec_938069,Human_Splice_Rec_938113 82616 RMVar_ID_82616 Human_SNP_ID_345208835 m1A Human chr7 + 151059754 151059754 151059754 AGACCCCGAGACCCCCGGGGCACGAAGTCCAGAGCGAGCGGGTAGGCGGAGAGGTGGTGGCGGGG AGACCCCGAGACCCCCGGGGCACGAAGTCCAGTGCGAGCGGGTAGGCGGAGAGGTGGTGGCGGGG A T SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:151059601..151059818;chr7:151059576..151059807;chr7:151059576..151059833;chr7:151059601..151059823 26863196 MeRIP-seq:(Medium) rs910355144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956048,Human_RBP_ID_8944214,Human_RBP_ID_9312068,Human_RBP_ID_18426462,Human_RBP_ID_26772279 Human_Splice_Rec_938069,Human_Splice_Rec_938113 82617 RMVar_ID_82617 Human_SNP_ID_345208836 m1A Human chr7 - 151059764 151059764 151059764 CCTGGCCGTCCCCCGCCACCACCTCTCCGCCTACCCGCTCGCTCTGGACTTCGTGCCCCGGGGGT CCTGGCCGTCCCCCGCCACCACCTCTCCGCCTCCCCGCTCGCTCTGGACTTCGTGCCCCGGGGGT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:151059674..151059775 26863410 MeRIP-seq:(Medium) rs1334326608 Functional Loss SNV dbSNP153 33..33 33 - - - 82618 RMVar_ID_82618 Human_SNP_ID_345210314 m1A Human chr7 + 151064682 151064682 151064682 GACTGGAGAAACCCCGACCATTGAGGAGGGGGAGGAAGATGAGGATGAGGCCAGCGAGGCTGAGG GACTGGAGAAACCCCGACCATTGAGGAGGGGGGGGAAGATGAGGATGAGGCCAGCGAGGCTGAGG A G SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151064474..151064783 26863196 MeRIP-seq:(Medium) rs760651726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85456,Human_RBP_ID_253686,Human_RBP_ID_843755,Human_RBP_ID_3971553 Human_Splice_Rec_938031,Human_Splice_Rec_938075,Human_Splice_Rec_938123,Human_Splice_Rec_938143,Human_Splice_Rec_938185 RMVar_hsa_circ_58653,RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_249417 82619 RMVar_ID_82619 Human_SNP_ID_345210318 m1A Human chr7 + 151064694 151064694 151064694 CCCGACCATTGAGGAGGGGGAGGAAGATGAGGATGAGGCCAGCGAGGCTGAGGGGGCCCGGGCTC CCCGACCATTGAGGAGGGGGAGGAAGATGAGGTTGAGGCCAGCGAGGCTGAGGGGGCCCGGGCTC A T SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:151064485..151064750;chr7:151064485..151064694 26863196 MeRIP-seq:(Medium) rs770874767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85456,Human_RBP_ID_253686,Human_RBP_ID_843755,Human_RBP_ID_3971553,Human_RBP_ID_5220373,Human_RBP_ID_18472406 Human_Splice_Rec_938031,Human_Splice_Rec_938075,Human_Splice_Rec_938123,Human_Splice_Rec_938143,Human_Splice_Rec_938185 RMVar_hsa_circ_58653,RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_249417 82620 RMVar_ID_82620 Human_SNP_ID_345210915 m1A Human chr7 - 151066577 151066577 151066577 GGCAGGGGGCGCCCCGAGGCACCCCCGTCGTCACCCCCTGCAGTGCCACTGGCCACCGCCACCGC GGCAGGGGGCGCCCCGAGGCACCCCCGTCGTCCCCCCCTGCAGTGCCACTGGCCACCGCCACCGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151066526..151066686 26863196 MeRIP-seq:(Medium) rs775944006 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 82621 RMVar_ID_82621 Human_SNP_ID_345212008 m1A Human chr7 + 151070076 151070076 151070076 CAGGGCCAACGTGCTGCGGGCTCTGCTGTTGAAACACAGGTGAGGCCCTGTGGGCCAGTTGGGGA CAGGGCCAACGTGCTGCGGGCTCTGCTGTTGAGACACAGGTGAGGCCCTGTGGGCCAGTTGGGGA A G SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:151066592..151070507 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18472408,Human_RBP_ID_27568962 Human_Splice_Rec_938041,Human_Splice_Rec_938085,Human_Splice_Rec_938153,Human_Splice_Rec_938195 Human_miRNA_ID_2586802,Human_miRNA_ID_2586803 RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_108385,RMVar_hsa_circ_249417,RMVar_hsa_circ_249418 82622 RMVar_ID_82622 Human_SNP_ID_345212587 m1A Human chr7 + 151071498 151071498 151071498 GCTGATCCGAGATGTGCGGCGCCGCTATCCCCACTACCTGAGTGACTTCCGAGATGCACTTGACC GCTGATCCGAGATGTGCGGCGCCGCTATCCCCGCTACCTGAGTGACTTCCGAGATGCACTTGACC A G SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151071399..151071546 26863196 MeRIP-seq:(Medium) rs150503454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1330942,Human_RBP_ID_8915196 82623 RMVar_ID_82623 Human_SNP_ID_345212588 m1A Human chr7 + 151071498 151071498 151071498 GCTGATCCGAGATGTGCGGCGCCGCTATCCCCACTACCTGAGTGACTTCCGAGATGCACTTGACC GCTGATCCGAGATGTGCGGCGCCGCTATCCCCTCTACCTGAGTGACTTCCGAGATGCACTTGACC A T SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151071399..151071546 26863196 MeRIP-seq:(Medium) rs150503454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1330942,Human_RBP_ID_8915196 82624 RMVar_ID_82624 Human_SNP_ID_345213921 m1A Human chr7 - 151075757 151075757 151075757 GCTGGGGGGCTCACCTTCTTGACGTAAGTGACATCTGGGTGGTGTTTGGGCGGCATGAGCAGCAG GCTGGGGGGCTCACCTTCTTGACGTAAGTGACTTCTGGGTGGTGTTTGGGCGGCATGAGCAGCAG T A AC010973.2 Ensembl:ENSG00000244151 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151075707..151075809 26863196 MeRIP-seq:(Medium) rs768049855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624713 82625 RMVar_ID_82625 Human_SNP_ID_345214481 m1A Human chr7 + 151077156 151077156 151077156 GGCGCTAGAGGCAGCCTGGCCCTGTGGGCAGGACCTTGGTGGGTATGGCAGGAAGGGGTCCTGGG GGCGCTAGAGGCAGCCTGGCCCTGTGGGCAGGCCCTTGGTGGGTATGGCAGGAAGGGGTCCTGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151077041..151077248 26863196 MeRIP-seq:(Medium) rs1461381892 Functional Loss SNV dbSNP153 33..33 33 - - - 82626 RMVar_ID_82626 Human_SNP_ID_345214512 m1A Human chr7 + 151077225 151077225 151077225 CACGGGAAGCACAGCACCAGAGCTGCTGGCGCACAGCAGGAAGTCTGGAGGGGAGCAGGGCCGGC CACGGGAAGCACAGCACCAGAGCTGCTGGCGCGCAGCAGGAAGTCTGGAGGGGAGCAGGGCCGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr7:151077176..151077375;chr7:151076691..151077235 26863196,32194978 MeRIP-seq:(Medium) rs1451577957 Functional Loss SNV dbSNP153 33..33 33 - - - 82627 RMVar_ID_82627 Human_SNP_ID_345215123 m1A Human chr7 - 151078951 151078951 151078951 CAGGAGCGAAGGCTCCGCCTCCCTCCGAAGCCACCTCCCCCTTTGCAGCCCCTTCTCCGAGGTGG CAGGAGCGAAGGCTCCGCCTCCCTCCGAAGCCGCCTCCCCCTTTGCAGCCCCTTCTCCGAGGTGG T C FASTK Ensembl:ENSG00000164896 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151078901..151079000 26863196 MeRIP-seq:(Medium) rs775058397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_938250,Human_Splice_Rec_938262,Human_Splice_Rec_938263,Human_Splice_Rec_938280,Human_Splice_Rec_938308,Human_Splice_Rec_938326,Human_Splice_Rec_938327,Human_Splice_Rec_938342,Human_Splice_Rec_938366,Human_Splice_Rec_938391,Human_Splice_Rec_938402,Human_Splice_Rec_938403 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 82628 RMVar_ID_82628 Human_SNP_ID_345215436 m1A Human chr7 + 151079892 151079892 151079892 GCCGAGCAGGGGAGGTCTGAGCAGAGAGCAGGACTCGAAGCATGGAGTTGGGTGATGGAGACCCT GCCGAGCAGGGGAGGTCTGAGCAGAGAGCAGGGCTCGAAGCATGGAGTTGGGTGATGGAGACCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151079841..151079939 26863196 MeRIP-seq:(Medium) rs1344190762 Functional Loss SNV dbSNP153 33..33 33 - - - 82629 RMVar_ID_82629 Human_SNP_ID_345215440 m1A Human chr7 - 151079902 151079902 151079902 GCTGCCCCTCAGGGTCTCCATCACCCAACTCCATGCTTCGAGTCCTGCTCTCTGCTCAGACCTCC GCTGCCCCTCAGGGTCTCCATCACCCAACTCCTTGCTTCGAGTCCTGCTCTCTGCTCAGACCTCC T A FASTK Ensembl:ENSG00000164896 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151079851..151079925 26863196 MeRIP-seq:(Medium) rs779709184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4961265,Human_RBP_ID_16067852,Human_RBP_ID_17424762,Human_RBP_ID_18878349,Human_RBP_ID_22686116,Human_RBP_ID_22833978,Human_RBP_ID_27107917 Human_Splice_Rec_938248,Human_Splice_Rec_938278,Human_Splice_Rec_938324,Human_Splice_Rec_938364,Human_Splice_Rec_938410 Human_miRNA_ID_1998052,Human_miRNA_ID_2251902 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 82630 RMVar_ID_82630 Human_SNP_ID_345215441 m1A Human chr7 - 151079902 151079902 151079902 GCTGCCCCTCAGGGTCTCCATCACCCAACTCCATGCTTCGAGTCCTGCTCTCTGCTCAGACCTCC GCTGCCCCTCAGGGTCTCCATCACCCAACTCCGTGCTTCGAGTCCTGCTCTCTGCTCAGACCTCC T C FASTK Ensembl:ENSG00000164896 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151079851..151079925 26863196 MeRIP-seq:(Medium) rs779709184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4961265,Human_RBP_ID_16067852,Human_RBP_ID_17424762,Human_RBP_ID_18878349,Human_RBP_ID_22686116,Human_RBP_ID_22833978,Human_RBP_ID_27107917 Human_Splice_Rec_938248,Human_Splice_Rec_938278,Human_Splice_Rec_938324,Human_Splice_Rec_938364,Human_Splice_Rec_938410 Human_miRNA_ID_1998052,Human_miRNA_ID_2251902 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 82631 RMVar_ID_82631 Human_SNP_ID_345215896 m1A Human chr7 - 151081269 151081250 151081270 GGGCATCTGCTGTCGCTGCCTCGGCCCCGGGCAGAGCCGGGCCGCCCCGGGGGCCCGTCTTAGTG GGGCATCTGCTGTCGCTGCCTCGGCCCCGGG____________________GGCCCGTCTTAGTG CCCCGGGGCGGCCCGGCTCTG C TMUB1 Ensembl:ENSG00000164897 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:151081226..151081324 32194978 MeRIP-seq:(Medium) rs552241949 Functional Loss DEL dbSNP153 32..51 33 - - - Human_RBP_ID_678891,Human_RBP_ID_5153101,Human_RBP_ID_5243351,Human_RBP_ID_26551827,Human_RBP_ID_27529676 Human_miRNA_ID_929533,Human_miRNA_ID_2386697,Human_miRNA_ID_2388172,Human_miRNA_ID_2395089,Human_miRNA_ID_2399323,Human_miRNA_ID_3030373,Human_miRNA_ID_3068782 RMVar_hsa_circ_249423,RMVar_hsa_circ_101501 82632 RMVar_ID_82632 Human_SNP_ID_345215978 m1A Human chr7 - 151081528 151081528 151081528 TACCGCCCGTAGTGCCTCCGCGGGCGCTTGGCAGCGTCGCCGGCCCCTCCGGACCTTGCTCCCCG TACCGCCCGTAGTGCCTCCGCGGGCGCTTGGCTGCGTCGCCGGCCCCTCCGGACCTTGCTCCCCG T A TMUB1 Ensembl:ENSG00000164897 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:151081451..151081795 26863196 MeRIP-seq:(Medium) rs1563392233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678896,Human_RBP_ID_22463832,Human_RBP_ID_27529685 Human_miRNA_ID_2390074,Human_miRNA_ID_2591312 RMVar_hsa_circ_249423,RMVar_hsa_circ_101501 82633 RMVar_ID_82633 Human_SNP_ID_345216140 m1A Human chr7 + 151081893 151081893 151081893 GATGAGTCGCACCTGCTGTTCCCGGCCGGGAAACTGGGTCCTGAGGAGAGAGGGACCTGGGTAAG GATGAGTCGCACCTGCTGTTCCCGGCCGGGAATCTGGGTCCTGAGGAGAGAGGGACCTGGGTAAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:151081470..151082185 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 82634 RMVar_ID_82634 Human_SNP_ID_345216263 m1A Human chr7 - 151082265 151082265 151082265 CACAGCAACACCGCCAGCCCCGGACTCCCCGCAGGAGCCCCTCGTGCTACGGCTGAAATTCCTCA CACAGCAACACCGCCAGCCCCGGACTCCCCGCGGGAGCCCCTCGTGCTACGGCTGAAATTCCTCA T C TMUB1 Ensembl:ENSG00000164897 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151082220..151083472 26863196 MeRIP-seq:(Medium) rs1286727483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_678911,Human_RBP_ID_4931119,Human_RBP_ID_26831894 Human_Splice_Rec_938411,Human_Splice_Rec_938415,Human_Splice_Rec_938417,Human_Splice_Rec_938419,Human_Splice_Rec_938423,Human_Splice_Rec_938427,Human_Splice_Rec_938431,Human_Splice_Rec_938435 82635 RMVar_ID_82635 Human_SNP_ID_345216489 m1A Human chr7 + 151082906 151082906 151082906 CCTAAGCAACGCCTCTCCTAAACTTCACCCCAACCAAACTTCACCCCCAAGCGTATCTATTCTCC CCTAAGCAACGCCTCTCCTAAACTTCACCCCAGCCAAACTTCACCCCCAAGCGTATCTATTCTCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:151082595..151082952 26863196 MeRIP-seq:(Medium) rs1180145855 Functional Loss SNV dbSNP153 33..33 33 - - - 82636 RMVar_ID_82636 Human_SNP_ID_345216498 m1A Human chr7 + 151082928 151082928 151082928 CTTCACCCCAACCAAACTTCACCCCCAAGCGTATCTATTCTCCTGCCCACTTCACCCCAGTGTGT CTTCACCCCAACCAAACTTCACCCCCAAGCGTGTCTATTCTCCTGCCCACTTCACCCCAGTGTGT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:151082814..151082969 26863196 MeRIP-seq:(Medium) rs1381268656 Functional Loss SNV dbSNP153 33..33 33 - - - 82637 RMVar_ID_82637 Human_SNP_ID_345217671 m1A Human chr7 - 151086922 151086922 151086922 GGCCCGGATGGCCGCGGAGTTGGAGAGCGCGAACTGCTGGGGGGGCCCGCCGGCCAGCTGCTGCG GGCCCGGATGGCCGCGGAGTTGGAGAGCGCGAGCTGCTGGGGGGGCCCGCCGGCCAGCTGCTGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151086876..151086977 26863196 MeRIP-seq:(Medium) rs1406302269 Functional Loss SNV dbSNP153 33..33 33 - - - 82638 RMVar_ID_82638 Human_SNP_ID_345222270 m1A Human chr7 + 151104914 151104914 151104914 TACTGTGAGATGCTATGAAGCCAGGCCACCGGAGCAAGCTAGAGCCAACCCAGTGGCCTGGGGAG TACTGTGAGATGCTATGAAGCCAGGCCACCGGGGCAAGCTAGAGCCAACCCAGTGGCCTGGGGAG A G AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151104909..151105046 26863196 MeRIP-seq:(Medium) rs1251453869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8661969,Human_RBP_ID_16068353 RMVar_hsa_circ_249424,RMVar_hsa_circ_105264,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425 82639 RMVar_ID_82639 Human_SNP_ID_345223736 m1A Human chr7 + 151110378 151110378 151110378 AGATGGTCAGCCTCCCAAGGAAGGGATGCTTCAGCCACGGTCCAAATGCCTTCAGGGACAAGCAG AGATGGTCAGCCTCCCAAGGAAGGGATGCTTCGGCCACGGTCCAAATGCCTTCAGGGACAAGCAG A G AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151110374..151110538 26863196 MeRIP-seq:(Medium) rs1045175163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249424,RMVar_hsa_circ_105264,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425 82640 RMVar_ID_82640 Human_SNP_ID_345227309 m1A Human chr7 + 151121526 151121526 151121526 CTCCCCTTCCCCTCGTTGGCAAGCTCTGTAGCAACCCCAGGGCACCCCCTGCCTTTCCCTGCCCT CTCCCCTTCCCCTCGTTGGCAAGCTCTGTAGCGACCCCAGGGCACCCCCTGCCTTTCCCTGCCCT A G AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151121520..151121729 26863196 MeRIP-seq:(Medium) rs554092887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17093066,Human_RBP_ID_18959747,Human_RBP_ID_21458684 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_249426,RMVar_hsa_circ_303719,RMVar_hsa_circ_367215,RMVar_hsa_circ_308181,RMVar_hsa_circ_249427,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_249434,RMVar_hsa_circ_249432,RMVar_hsa_circ_357571,RMVar_hsa_circ_375169,RMVar_hsa_circ_352425,RMVar_hsa_circ_249433 82641 RMVar_ID_82641 Human_SNP_ID_345227869 m1A Human chr7 - 151123226 151123224 151123226 CGGATCCTAGGAAATAGGGGGAGGCCAAAAAGAGGGGGCAAGGCAAGCGCGGCGGCGGCGGCGGC CGGATCCTAGGAAATAGGGGGAGGCCAAAAAG__GGGGCAAGGCAAGCGCGGCGGCGGCGGCGGC CCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:151123176..151123507 26863196 MeRIP-seq:(Medium) rs879617716 Functional Loss DEL dbSNP153 33..34 33 - - - 82642 RMVar_ID_82642 Human_SNP_ID_345227873 m1A Human chr7 - 151123226 151123226 151123226 CGGATCCTAGGAAATAGGGGGAGGCCAAAAAGAGGGGGCAAGGCAAGCGCGGCGGCGGCGGCGGC CGGATCCTAGGAAATAGGGGGAGGCCAAAAAGCGGGGGCAAGGCAAGCGCGGCGGCGGCGGCGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:151123176..151123507 26863196 MeRIP-seq:(Medium) rs967660829 Functional Loss SNV dbSNP153 33..33 33 - - - 82643 RMVar_ID_82643 Human_SNP_ID_345227972 m1A Human chr7 - 151123504 151123504 151123504 GGGCGCGAGGAGCACGCCCGGGGCGGGGGCGTAAGAGAAGCGGGGGCGAGGAGGTGGACGGTGGG GGGCGCGAGGAGCACGCCCGGGGCGGGGGCGTGAGAGAAGCGGGGGCGAGGAGGTGGACGGTGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151123467..151123630 26863196 MeRIP-seq:(Medium) rs1468851368 Functional Loss SNV dbSNP153 33..33 33 - - - 82644 RMVar_ID_82644 Human_SNP_ID_345228850 m1A Human chr7 + 151126289 151126274 151126289 GTGCGGAGACCCCTTCCCGCCCTGACTGTCGGAGAAACCGCGCGCAGTGCAGGCCTTGAGGGGCT GTGCGGAGACCCCTTCCC_______________GAAACCGCGCGCAGTGCAGGCCTTGAGGGGCT CGCCCTGACTGTCGGA C AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151126283..151126351 26863196 MeRIP-seq:(Medium) rs141643830 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_18426466,Human_RBP_ID_22703850,Human_RBP_ID_24388914 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_303719,RMVar_hsa_circ_367215,RMVar_hsa_circ_249427,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_3325,RMVar_hsa_circ_249434,RMVar_hsa_circ_249432,RMVar_hsa_circ_357571,RMVar_hsa_circ_375169,RMVar_hsa_circ_352425,RMVar_hsa_circ_249433,RMVar_hsa_circ_85626,RMVar_hsa_circ_331841,RMVar_hsa_circ_249439 82645 RMVar_ID_82645 Human_SNP_ID_345230066 m1A Human chr7 + 151130492 151130490 151130492 TTGCCAAGAGCACCTCCCTCTGGGGCTGGCTGAGAGAGTCATGTAAGAGTTAATAGCAGGGTGAG TTGCCAAGAGCACCTCCCTCTGGGGCTGGCT__GAGAGTCATGTAAGAGTTAATAGCAGGGTGAG TGA T AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151130488..151130637 26863196 MeRIP-seq:(Medium) rs1296713682 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_16068486 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_367215,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_3325,RMVar_hsa_circ_249432,RMVar_hsa_circ_375169,RMVar_hsa_circ_249433,RMVar_hsa_circ_85626,RMVar_hsa_circ_331841,RMVar_hsa_circ_28137,RMVar_hsa_circ_92015,RMVar_hsa_circ_249439,RMVar_hsa_circ_249440 82646 RMVar_ID_82646 Human_SNP_ID_345232682 m1A Human chr7 + 151140074 151140074 151140074 CCAACCGGAAGAAGCACCGGAGGAAAAAGAGCACCGGGACCCCCCGACCAGACGGCCCCAGCAGT CCAACCGGAAGAAGCACCGGAGGAAAAAGAGCGCCGGGACCCCCCGACCAGACGGCCCCAGCAGT A G AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:151140027..151140128 32194978 MeRIP-seq:(Medium) rs767911248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26357312,Human_RBP_ID_27829982 Human_Splice_Rec_938498,Human_Splice_Rec_938499,Human_Splice_Rec_938562,Human_Splice_Rec_938563,Human_Splice_Rec_938682,Human_Splice_Rec_938683 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_249432,RMVar_hsa_circ_85626,RMVar_hsa_circ_331841,RMVar_hsa_circ_92015,RMVar_hsa_circ_249439,RMVar_hsa_circ_249440,RMVar_hsa_circ_110713,RMVar_hsa_circ_249442 82647 RMVar_ID_82647 Human_SNP_ID_345233843 m1A Human chr7 + 151144089 151144089 151144089 ACGAAGCCAAGGAAATTAGGGAGGAGAGTCAAAGGGATCAAGGAGAGTTGGGGATTTGAGCTGCA ACGAAGCCAAGGAAATTAGGGAGGAGAGTCAAGGGGATCAAGGAGAGTTGGGGATTTGAGCTGCA A G AGAP3 Ensembl:ENSG00000133612 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:151143798..151144180;chr7:151143984..151144189 26863196 MeRIP-seq:(Medium) rs766760343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3071485,Human_RBP_ID_3971602,Human_RBP_ID_5153346,Human_RBP_ID_8146459,Human_RBP_ID_8662007,Human_RBP_ID_17712599,Human_RBP_ID_18095621,Human_RBP_ID_18171974,Human_RBP_ID_18196466,Human_RBP_ID_18380115,Human_RBP_ID_27353996,Human_RBP_ID_27529718 Human_miRNA_ID_445742,Human_miRNA_ID_545896,Human_miRNA_ID_581135,Human_miRNA_ID_2142130,Human_miRNA_ID_2192923,Human_miRNA_ID_2207132,Human_miRNA_ID_3045936 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_249432,RMVar_hsa_circ_92015,RMVar_hsa_circ_249440,RMVar_hsa_circ_110713,RMVar_hsa_circ_249442 82648 RMVar_ID_82648 Human_SNP_ID_345251589 m1A Human chr7 - 151212645 151212645 151212645 CTCTACAAATAGTAATAAAATGAACCGGGCATAGTAGCATGTGCCTGCGGTCCCAGCTGCTCTGA CTCTACAAATAGTAATAAAATGAACCGGGCATGGTAGCATGTGCCTGCGGTCCCAGCTGCTCTGA T C ABCF2,ABCF2:2 Ensembl:ENSG00000285292,Ensembl:ENSG00000033050 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1065071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_679015,Human_RBP_ID_1683632,Human_RBP_ID_16068785,Human_RBP_ID_26544977 GWAS_ID_10009,GWAS_ID_10010,GWAS_ID_10011,GWAS_ID_10012,GWAS_ID_10013 RMVar_hsa_circ_117046,RMVar_hsa_circ_249443 82649 RMVar_ID_82649 Human_SNP_ID_345255246 m1A Human chr7 - 151226406 151226406 151226406 GAAGAAGGCAGCCAAAAAGAAGGAGGCTGCCAAAGCTCGACAGCGGCCCAGAAAAGGACATGAAG GAAGAAGGCAGCCAAAAAGAAGGAGGCTGCCAGAGCTCGACAGCGGCCCAGAAAAGGACATGAAG T C ABCF2,ABCF2:2 Ensembl:ENSG00000285292,Ensembl:ENSG00000033050 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151226355..151226437 26863196 MeRIP-seq:(Medium) rs1317447930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86662,Human_RBP_ID_4961356,Human_RBP_ID_9404088,Human_RBP_ID_26357326,Human_RBP_ID_26831898 Human_Splice_Rec_938798,Human_Splice_Rec_938828,Human_Splice_Rec_938876,Human_Splice_Rec_938884 RMVar_hsa_circ_339368,RMVar_hsa_circ_29419,RMVar_hsa_circ_20864,RMVar_hsa_circ_89453,RMVar_hsa_circ_249446 82650 RMVar_ID_82650 Human_SNP_ID_345256883 m1A Human chr7 - 151232746 151232746 151232746 GCCAGAGACAGCATCGAGGCCGCGAGCGCAGGACCAGGAGGGACGCCCAAGGCCCTCGGGGAGGA GCCAGAGACAGCATCGAGGCCGCGAGCGCAGGCCCAGGAGGGACGCCCAAGGCCCTCGGGGAGGA T G lnc-ABCF2-2 RNACentral:URS00008B30C0 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151232574..151232900 26863196 MeRIP-seq:(Medium) rs767896569 Functional Loss SNV dbSNP153 33..33 33 - - - 82651 RMVar_ID_82651 Human_SNP_ID_345256926 m1A Human chr7 + 151232848 151232845 151232848 TCTGTGCCCCAGTCTCCCAGCCGCGACCTCCGACCCCGCCTCGCAGAACGACCCGAGCTGGTCTC TCTGTGCCCCAGTCTCCCAGCCGCGACCTC___CCCCGCCTCGCAGAACGACCCGAGCTGGTCTC CCGA C CHPF2 Ensembl:ENSG00000033100 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151232801..151232902 26863196 MeRIP-seq:(Medium) rs1348448093 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_679048,Human_RBP_ID_794760,Human_RBP_ID_4956062,Human_RBP_ID_8150729 82652 RMVar_ID_82652 Human_SNP_ID_345261262 m1A Human chr7 + 151246863 151246860 151246863 GTGGGATGGGGACTGGGACCACGAAAGCAGGAAGAAGATCAGAGGGCAGGGGATGCAGACCCTGG GTGGGATGGGGACTGGGACCACGAAAGCAG___GAAGATCAGAGGGCAGGGGATGCAGACCCTGG GGAA G RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151246858..151247135 26863196 MeRIP-seq:(Medium) rs1007370212 Functional Loss DEL dbSNP153 31..33 33 - - - 82653 RMVar_ID_82653 Human_SNP_ID_345261694 m1A Human chr7 - 151248512 151248512 151248512 GCCGGAGGGGCGCGCAAAGCCACGAAAAGCAAACTTTTTGAGTTTCTGGTCCATGGGGTGGTGAG GCCGGAGGGGCGCGCAAAGCCACGAAAAGCAAGCTTTTTGAGTTTCTGGTCCATGGGGTGGTGAG T C SMARCD3 Ensembl:ENSG00000082014 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:151248511..151248670 26863196 MeRIP-seq:(Medium) rs1173695494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_938909,Human_Splice_Rec_939027,Human_Splice_Rec_939041 RMVar_hsa_circ_91809,RMVar_hsa_circ_249448 82654 RMVar_ID_82654 Human_SNP_ID_345287328 m1A Human chr7 - 151345320 151345320 151345320 CATCCCTGAAAGCAAAACAATACATTAATAAAACTCCACATCGCATTTTAAAATGTTAATAACTT CATCCCTGAAAGCAAAACAATACATTAATAAAGCTCCACATCGCATTTTAAAATGTTAATAACTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151345318..151345406 26863196 MeRIP-seq:(Medium) rs1412298564 Functional Loss SNV dbSNP153 33..33 33 - - - 82655 RMVar_ID_82655 Human_SNP_ID_345289890 m1A Human chr7 + 151355947 151355947 151355947 GGACCAAGAGAGGACTAGAAATACTGGCAAAGAGAGGTACCCAGAGCTCTGGGCTTGTCACCCAC GGACCAAGAGAGGACTAGAAATACTGGCAAAGTGAGGTACCCAGAGCTCTGGGCTTGTCACCCAC A T NUB1 Ensembl:ENSG00000013374 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151355900..151356200 26863196 MeRIP-seq:(Medium) rs1266552568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843186,Human_RBP_ID_16069508,Human_RBP_ID_26358493 Human_Splice_Rec_939105,Human_Splice_Rec_939133,Human_Splice_Rec_939161,Human_Splice_Rec_939177,Human_Splice_Rec_939203,Human_Splice_Rec_939217,Human_Splice_Rec_939227,Human_Splice_Rec_939235,Human_Splice_Rec_939249 RMVar_hsa_circ_79679,RMVar_hsa_circ_73212,RMVar_hsa_circ_11909,RMVar_hsa_circ_56150,RMVar_hsa_circ_116164,RMVar_hsa_circ_309691,RMVar_hsa_circ_249451,RMVar_hsa_circ_249452,RMVar_hsa_circ_353596,RMVar_hsa_circ_249453 82656 RMVar_ID_82656 Human_SNP_ID_345289947 m1A Human chr7 + 151356146 151356146 151356146 TGGTTTTGTTACAGCAGCAGAGACAGTGGTGGATCCAGAAATGACACCGTACTTAGACATAGCTA TGGTTTTGTTACAGCAGCAGAGACAGTGGTGGTTCCAGAAATGACACCGTACTTAGACATAGCTA A T NUB1 Ensembl:ENSG00000013374 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151356126..151356175 26863196 MeRIP-seq:(Medium) rs780626926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16069511,Human_RBP_ID_26357334 Human_Splice_Rec_939106,Human_Splice_Rec_939107,Human_Splice_Rec_939134,Human_Splice_Rec_939135,Human_Splice_Rec_939162,Human_Splice_Rec_939163,Human_Splice_Rec_939178,Human_Splice_Rec_939179,Human_Splice_Rec_939204,Human_Splice_Rec_939205,Human_Splice_Rec_939218,Human_Splice_Rec_939219,Human_Splice_Rec_939228,Human_Splice_Rec_939229,Human_Splice_Rec_939236,Human_Splice_Rec_939237,Human_Splice_Rec_939250,Human_Splice_Rec_939251 RMVar_hsa_circ_73212,RMVar_hsa_circ_11909,RMVar_hsa_circ_56150,RMVar_hsa_circ_309691,RMVar_hsa_circ_249452,RMVar_hsa_circ_353596 82657 RMVar_ID_82657 Human_SNP_ID_345294024 m1A Human chr7 - 151372655 151372655 151372655 GCTACTCAGGGCCCCCACTCCCTGGCCCCAACAATGCTTCGAAACTGACCTTATCCTGCCACACC GCTACTCAGGGCCCCCACTCCCTGGCCCCAACGATGCTTCGAAACTGACCTTATCCTGCCACACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151372605..151372788 26863196 MeRIP-seq:(Medium) rs1414994792 Functional Loss SNV dbSNP153 33..33 33 - - - 82658 RMVar_ID_82658 Human_SNP_ID_345331369 m1A Human chr7 - 151519561 151519561 151519561 CGCGGCCGCCGCCGATCACAGCAGCAGGAGCCACCGCCGCCGCGGTTGATGTGGTTGGGCCGGGG CGCGGCCGCCGCCGATCACAGCAGCAGGAGCCGCCGCCGCCGCGGTTGATGTGGTTGGGCCGGGG T C RHEB Ensembl:ENSG00000106615 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr7:151519421..151519625;chr7:151519451..151519675 26863196,26863410 MeRIP-seq:(Medium) rs4015373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174330,Human_RBP_ID_679178,Human_RBP_ID_4931802,Human_RBP_ID_9337531,Human_RBP_ID_22534370,Human_RBP_ID_24200266 RMVar_hsa_circ_90529,RMVar_hsa_circ_249468 82659 RMVar_ID_82659 Human_SNP_ID_345359577 m1A Human chr7 - 151632304 151632304 151632304 GGCGGCGGCGGCGGCCTCGGGCGGGTGGGGGCAGCGCTCCCGCTCCGCCCCCGGCCCCCGCTGCC GGCGGCGGCGGCGGCCTCGGGCGGGTGGGGGCGGCGCTCCCGCTCCGCCCCCGGCCCCCGCTGCC T C PRKAG2 Ensembl:ENSG00000106617 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:151632238..151632339 26863410 MeRIP-seq:(Medium) rs1363917510 Functional Loss SNV dbSNP153 33..33 33 - - - 82660 RMVar_ID_82660 Human_SNP_ID_345398152 m1A Human chr7 - 151781308 151781308 151781308 TGAGGCCCAAGACCAGCCCCGGCTCTCCCAAAACCGTGTTCCCGTTCTCCTACCAGGAGTCCCCG TGAGGCCCAAGACCAGCCCCGGCTCTCCCAAAGCCGTGTTCCCGTTCTCCTACCAGGAGTCCCCG T C PRKAG2 Ensembl:ENSG00000106617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151781258..151781333 26863196 MeRIP-seq:(Medium) rs564137307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18095758 RMVar_hsa_circ_352576 82661 RMVar_ID_82661 Human_SNP_ID_345398153 m1A Human chr7 - 151781308 151781308 151781308 TGAGGCCCAAGACCAGCCCCGGCTCTCCCAAAACCGTGTTCCCGTTCTCCTACCAGGAGTCCCCG TGAGGCCCAAGACCAGCCCCGGCTCTCCCAAACCCGTGTTCCCGTTCTCCTACCAGGAGTCCCCG T G PRKAG2 Ensembl:ENSG00000106617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151781258..151781333 26863196 MeRIP-seq:(Medium) rs564137307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18095758 RMVar_hsa_circ_352576 82662 RMVar_ID_82662 Human_SNP_ID_345418087 m1A Human chr7 - 151854928 151854928 151854928 TGTGGAGAGTGGTGGAGGGTGGTGTGTGTGTAAAGTGGTGTGTGTGCTTTCCCCAGCTCCAGCCC TGTGGAGAGTGGTGGAGGGTGGTGTGTGTGTAGAGTGGTGTGTGTGCTTTCCCCAGCTCCAGCCC T C PRKAG2 Ensembl:ENSG00000106617 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151854920..151855003 26863196 MeRIP-seq:(Medium) rs1192887608 Functional Loss SNV dbSNP153 33..33 33 - - - 82663 RMVar_ID_82663 Human_SNP_ID_345425054 m1A Human chr7 - 151876651 151876651 151876651 GGGGAGGGAAGGAGGGGACCGAACCCCCGAGGAGTTTCGCAGAATCAACTTCTGGTTAGAGTTAT GGGGAGGGAAGGAGGGGACCGAACCCCCGAGGCGTTTCGCAGAATCAACTTCTGGTTAGAGTTAT T G PRKAG2 Ensembl:ENSG00000106617 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151876601..151876678 26863196 MeRIP-seq:(Medium) rs1372475716 Functional Loss SNV dbSNP153 33..33 33 - - - 82664 RMVar_ID_82664 Human_SNP_ID_345425329 m1A Human chr7 - 151877497 151877497 151877497 GCTGCGGCCGCCGCAGGGGTCTGGGCGCGGCGACGAGGGCGGCGTGGGGCGACGGGGAGCGGGAC GCTGCGGCCGCCGCAGGGGTCTGGGCGCGGCGGCGAGGGCGGCGTGGGGCGACGGGGAGCGGGAC T C lnc-PRKAG2-1 RNACentral:URS0000D5CB4C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151877455..151877765 26863196 MeRIP-seq:(Medium) rs971602850 Functional Loss SNV dbSNP153 33..33 33 - - - 82665 RMVar_ID_82665 Human_SNP_ID_345425371 m1A Human chr7 + 151877604 151877604 151877604 TCCCGGCGTCTCACTGTGTGCCCTACCCTTTGAAACACGCCCCCGCGCCCGCCCTGCCGTAGACC TCCCGGCGTCTCACTGTGTGCCCTACCCTTTGCAACACGCCCCCGCGCCCGCCCTGCCGTAGACC A C PRKAG2-AS1 Ensembl:ENSG00000239911 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:151877454..151877765 26863196 MeRIP-seq:(Medium) rs1453688367 Functional Loss SNV dbSNP153 33..33 33 - - - 82666 RMVar_ID_82666 Human_SNP_ID_345425435 m1A Human chr7 + 151877800 151877800 151877800 GCGCTGGGTGCGAGCAGGGTCTAGCCACCCCCACCCTCACCCCACCCCACCCCACCCTGCTTTTT GCGCTGGGTGCGAGCAGGGTCTAGCCACCCCCCCCCTCACCCCACCCCACCCCACCCTGCTTTTT A C PRKAG2-AS1 Ensembl:ENSG00000239911 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:151877701..151877802 26863410 MeRIP-seq:(Medium) rs1423502160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_940041,Human_Splice_Rec_940043 82667 RMVar_ID_82667 Human_SNP_ID_345463902 m1A Human chr7 - 152025872 152025872 152025872 GCCGCCTAGAGGGTACTCACCGCCTTGCCCGCAGCCCAGGATCGCCGCCTTCTGGGACTCGGGCT GCCGCCTAGAGGGTACTCACCGCCTTGCCCGCCGCCCAGGATCGCCGCCTTCTGGGACTCGGGCT T G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152025700..152025922 26863196 MeRIP-seq:(Medium) rs1350835299 Functional Loss SNV dbSNP153 33..33 33 - - - 82668 RMVar_ID_82668 Human_SNP_ID_345491186 m1A Human chr7 - 152135512 152135510 152135513 AACACAAAAATTTGAAAAAGTTAAAAAAAAAAAGGAGATGTGATTATGCTTACAGCTGCAGGACT AACACAAAAATTTGAAAAAGTTAAAAAAAAA___GAGATGTGATTATGCTTACAGCTGCAGGACT CCTT C KMT2C Ensembl:ENSG00000055609 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs558587201 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_679304,Human_RBP_ID_24200540 Human_miRNA_ID_219166,Human_miRNA_ID_674820 RMVar_hsa_circ_249485,RMVar_hsa_circ_115161,RMVar_hsa_circ_93711,RMVar_hsa_circ_249484 82669 RMVar_ID_82669 Human_SNP_ID_345497333 m1A Human chr7 - 152158977 152158977 152158977 GGAGGAAGTGAAACCAAGAAACAGCGAAGCAAACGGACTCAGAGGACGGGTGAGAAAGCAGCACC GGAGGAAGTGAAACCAAGAAACAGCGAAGCAAGCGGACTCAGAGGACGGGTGAGAAAGCAGCACC T C KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152158928..152159031 26863196 MeRIP-seq:(Medium) rs757422333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82806,Human_RBP_ID_842677,Human_RBP_ID_955126,Human_RBP_ID_5622691,Human_RBP_ID_16073937,Human_RBP_ID_22834128,Human_RBP_ID_24235703,Human_RBP_ID_24549051 Human_Splice_Rec_940312,Human_Splice_Rec_940428,Human_Splice_Rec_940544,Human_Splice_Rec_940660,Human_Splice_Rec_940692,Human_Splice_Rec_940782 Human_miRNA_ID_1192666 RMVar_hsa_circ_35840,RMVar_hsa_circ_53825,RMVar_hsa_circ_249485,RMVar_hsa_circ_93711,RMVar_hsa_circ_353406,RMVar_hsa_circ_371007,RMVar_hsa_circ_95295,RMVar_hsa_circ_249487,RMVar_hsa_circ_78271,RMVar_hsa_circ_67950,RMVar_hsa_circ_249488,RMVar_hsa_circ_249489,RMVar_hsa_circ_112488,RMVar_hsa_circ_105433,RMVar_hsa_circ_104026,RMVar_hsa_circ_249490,RMVar_hsa_circ_249491,RMVar_hsa_circ_117513,RMVar_hsa_circ_249495,RMVar_hsa_circ_249497,RMVar_hsa_circ_93406,RMVar_hsa_circ_249496,RMVar_hsa_circ_70393,RMVar_hsa_circ_115854,RMVar_hsa_circ_105512,RMVar_hsa_circ_249499,RMVar_hsa_circ_249500,RMVar_hsa_circ_86552,RMVar_hsa_circ_119772,RMVar_hsa_circ_249502,RMVar_hsa_circ_249504,RMVar_hsa_circ_96423,RMVar_hsa_circ_249506,RMVar_hsa_circ_12060,RMVar_hsa_circ_266149,RMVar_hsa_circ_71744,RMVar_hsa_circ_96153,RMVar_hsa_circ_117278,RMVar_hsa_circ_106938,RMVar_hsa_circ_249508,RMVar_hsa_circ_249509,RMVar_hsa_circ_110467,RMVar_hsa_circ_249512,RMVar_hsa_circ_81858,RMVar_hsa_circ_91356,RMVar_hsa_circ_249514,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_249513,RMVar_hsa_circ_88736,RMVar_hsa_circ_335718,RMVar_hsa_circ_249517,RMVar_hsa_circ_356514,RMVar_hsa_circ_92762,RMVar_hsa_circ_55638,RMVar_hsa_circ_120523,RMVar_hsa_circ_39235,RMVar_hsa_circ_44119,RMVar_hsa_circ_249518,RMVar_hsa_circ_249519,RMVar_hsa_circ_268402,RMVar_hsa_circ_67222,RMVar_hsa_circ_100181,RMVar_hsa_circ_60539,RMVar_hsa_circ_249520,RMVar_hsa_circ_249521 82670 RMVar_ID_82670 Human_SNP_ID_345502535 m1A Human chr7 - 152177748 152177748 152177748 ATATTGAACTGAGACATAGGGCTCCTGACGGAAGGCAACGGCTGCCTTTCAGTGCTCCACCTGGC ATATTGAACTGAGACATAGGGCTCCTGACGGAGGGCAACGGCTGCCTTTCAGTGCTCCACCTGGC T C KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:152177652..152177778 26863196 MeRIP-seq:(Medium) rs938283942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173785,Human_RBP_ID_842682,Human_RBP_ID_5533773,Human_RBP_ID_5628249,Human_RBP_ID_9311630,Human_RBP_ID_16074189 Human_miRNA_ID_107940,Human_miRNA_ID_694606,Human_miRNA_ID_1018171,Human_miRNA_ID_1304629,Human_miRNA_ID_1380267,Human_miRNA_ID_1409460,Human_miRNA_ID_1498974,Human_miRNA_ID_2719877 RMVar_hsa_circ_14859,RMVar_hsa_circ_249485,RMVar_hsa_circ_93711,RMVar_hsa_circ_371007,RMVar_hsa_circ_95295,RMVar_hsa_circ_249487,RMVar_hsa_circ_78271,RMVar_hsa_circ_249488,RMVar_hsa_circ_249489,RMVar_hsa_circ_112488,RMVar_hsa_circ_105433,RMVar_hsa_circ_104026,RMVar_hsa_circ_249490,RMVar_hsa_circ_249491,RMVar_hsa_circ_117513,RMVar_hsa_circ_249495,RMVar_hsa_circ_249497,RMVar_hsa_circ_93406,RMVar_hsa_circ_249496,RMVar_hsa_circ_70393,RMVar_hsa_circ_105512,RMVar_hsa_circ_249499,RMVar_hsa_circ_86552,RMVar_hsa_circ_119772,RMVar_hsa_circ_249502,RMVar_hsa_circ_249504,RMVar_hsa_circ_96423,RMVar_hsa_circ_249506,RMVar_hsa_circ_266149,RMVar_hsa_circ_96153,RMVar_hsa_circ_117278,RMVar_hsa_circ_106938,RMVar_hsa_circ_249508,RMVar_hsa_circ_249509,RMVar_hsa_circ_110467,RMVar_hsa_circ_249512,RMVar_hsa_circ_81858,RMVar_hsa_circ_91356,RMVar_hsa_circ_249514,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_249513,RMVar_hsa_circ_88736,RMVar_hsa_circ_249517,RMVar_hsa_circ_356514,RMVar_hsa_circ_55638,RMVar_hsa_circ_120523,RMVar_hsa_circ_39235,RMVar_hsa_circ_44119,RMVar_hsa_circ_268402,RMVar_hsa_circ_100181,RMVar_hsa_circ_58965,RMVar_hsa_circ_63801,RMVar_hsa_circ_249520,RMVar_hsa_circ_249521,RMVar_hsa_circ_60406,RMVar_hsa_circ_107329,RMVar_hsa_circ_126045,RMVar_hsa_circ_22292,RMVar_hsa_circ_103844,RMVar_hsa_circ_249523,RMVar_hsa_circ_267735,RMVar_hsa_circ_43583,RMVar_hsa_circ_317611,RMVar_hsa_circ_249524,RMVar_hsa_circ_353892,RMVar_hsa_circ_249526,RMVar_hsa_circ_269348,RMVar_hsa_circ_307685,RMVar_hsa_circ_88453,RMVar_hsa_circ_249527,RMVar_hsa_circ_278916,RMVar_hsa_circ_249528,RMVar_hsa_circ_249529 82671 RMVar_ID_82671 Human_SNP_ID_345571705 m1A Human chr7 + 152428974 152428974 152428974 TTCAAGAACTATCACAGCTTGGCCTCACCACTACACACAGCCTCTGTTCTAGTCACACAGTCAGA TTCAAGAACTATCACAGCTTGGCCTCACCACTGCACACAGCCTCTGTTCTAGTCACACAGTCAGA A G RF00017-1166,RF00017-4520 RNACentral:URS00009832A9,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152428963..152429098 26863196 MeRIP-seq:(Medium) rs938181286 Functional Loss SNV dbSNP153 33..33 33 - - - 82672 RMVar_ID_82672 Human_SNP_ID_345573680 m1A Human chr7 - 152435749 152435749 152435749 GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCAGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCGGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG T C KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152435703..152435783 26863196 MeRIP-seq:(Medium) rs866392536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252986,Human_RBP_ID_842694,Human_RBP_ID_19021665,Human_RBP_ID_23080479 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 82673 RMVar_ID_82673 Human_SNP_ID_345573681 m1A Human chr7 - 152435749 152435749 152435749 GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCAGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCCGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG T G KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152435703..152435783 26863196 MeRIP-seq:(Medium) rs866392536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252986,Human_RBP_ID_842694,Human_RBP_ID_19021665,Human_RBP_ID_23080479 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 82674 RMVar_ID_82674 Human_SNP_ID_345574026 m1A Human chr7 + 152436360 152436360 152436360 CGCTGGGCGCCGGGCCGCGGCTCGCTCCTCACACTCGCTCTCTCACACACGCTCGCTCGCTCTCC CGCTGGGCGCCGGGCCGCGGCTCGCTCCTCACCCTCGCTCTCTCACACACGCTCGCTCGCTCTCC A C FABP5P3 Ensembl:ENSG00000241735 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152436266..152436550 26863196 MeRIP-seq:(Medium) rs1367650724 Functional Loss SNV dbSNP153 33..33 33 - - - 82675 RMVar_ID_82675 Human_SNP_ID_345574087 m1A Human chr7 + 152436525 152436525 152436525 GGCGACCCGCACCACAGACCTCTCCAACTCGCAGCCGTCGCGCCCACACACCGCCGCCTCGACGG GGCGACCCGCACCACAGACCTCTCCAACTCGCCGCCGTCGCGCCCACACACCGCCGCCTCGACGG A C FABP5P3 Ensembl:ENSG00000241735 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152436240..152436558 26863196 MeRIP-seq:(Medium) rs1421899094 Functional Loss SNV dbSNP153 33..33 33 - - - 82676 RMVar_ID_82676 Human_SNP_ID_345581843 m1A Human chr7 - 152464240 152464240 152464240 GGTCGGGGCAGAGCCGCCCGGGAAGCCGCGCGAGGACGGCGGCCGGCGGCCGGCGGCGGAGGCAG GGTCGGGGCAGAGCCGCCCGGGAAGCCGCGCGTGGACGGCGGCCGGCGGCCGGCGGCGGAGGCAG T A RF00017-4575,RF00017-4520 RNACentral:URS0000918622,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152464194..152464374 26863196 MeRIP-seq:(Medium) rs1202874307 Functional Loss SNV dbSNP153 33..33 33 - - - 82677 RMVar_ID_82677 Human_SNP_ID_345582048 m1A Human chr7 - 152464542 152464542 152464542 TCGCGGCTCCTCCCGGCTCCGCCCAGCGGCTCACCCCGCGGACGGGGATCCCTCCGCCCACCGCC TCGCGGCTCCTCCCGGCTCCGCCCAGCGGCTCGCCCCGCGGACGGGGATCCCTCCGCCCACCGCC T C RF00017-4575,RF00017-4520 RNACentral:URS0000918622,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152464492..152464737 26863196 MeRIP-seq:(Medium) rs1296261076 Functional Loss SNV dbSNP153 33..33 33 - - - 82678 RMVar_ID_82678 Human_SNP_ID_345582049 m1A Human chr7 + 152464544 152464544 152464544 CGGTGGGCGGAGGGATCCCCGTCCGCGGGGTGAGCCGCTGGGCGGAGCCGGGAGGAGCCGCGAGG CGGTGGGCGGAGGGATCCCCGTCCGCGGGGTGCGCCGCTGGGCGGAGCCGGGAGGAGCCGCGAGG A C LINC01003 Ensembl:ENSG00000261455 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152464498..152464729 26863196 MeRIP-seq:(Medium) rs542560616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867398,Human_RBP_ID_4956075,Human_RBP_ID_5222740,Human_RBP_ID_5328757,Human_RBP_ID_8220868,Human_RBP_ID_9337539,Human_RBP_ID_18426583 82679 RMVar_ID_82679 Human_SNP_ID_345582075 m1A Human chr7 + 152464574 152464574 152464574 TGAGCCGCTGGGCGGAGCCGGGAGGAGCCGCGAGGATCCGCAGTGGGGAGCCGGGAGGAACCTGG TGAGCCGCTGGGCGGAGCCGGGAGGAGCCGCGGGGATCCGCAGTGGGGAGCCGGGAGGAACCTGG A G LINC01003 Ensembl:ENSG00000261455 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:152464128..152464814 26863196 MeRIP-seq:(Medium) rs1564276766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867398,Human_RBP_ID_4956075,Human_RBP_ID_5328757,Human_RBP_ID_9338109,Human_RBP_ID_18426583 82680 RMVar_ID_82680 Human_SNP_ID_345631529 m1A Human chr7 - 152645914 152645914 152645914 TTTTTAAAATACATATTTGCTGTTTTATTTTTAGAGACAAGGTCTCGCTCCGTTGCCCAGGCTGG TTTTTAAAATACATATTTGCTGTTTTATTTTTCGAGACAAGGTCTCGCTCCGTTGCCCAGGCTGG T G XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1027073329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2038130,Human_RBP_ID_3073223,Human_RBP_ID_16077990,Human_RBP_ID_18878821,Human_RBP_ID_26545079,Human_RBP_ID_27108919 82681 RMVar_ID_82681 Human_SNP_ID_345663274 m1A Human chr7 - 152759892 152759892 152759892 GGTGCCACAGTCCACCACGCAGGGAGGCAGGGAGCCTGCCATGCTCGGGACGCGCGGCGCTCGGC GGTGCCACAGTCCACCACGCAGGGAGGCAGGGGGCCTGCCATGCTCGGGACGCGCGGCGCTCGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:152759835..152759920 26863410 MeRIP-seq:(Medium) rs1470083889 Functional Loss SNV dbSNP153 33..33 33 - - - 82682 RMVar_ID_82682 Human_SNP_ID_345669587 m1A Human chr7 + 152785451 152785451 152785451 GGGAGGGAGAGAGAGGGGGAGGGGGAGGGGGGAGAGGGGGGAGGGGGAGGGGGAGGGAGAGAGAG GGGAGGGAGAGAGAGGGGGAGGGGGAGGGGGGGGAGGGGGGAGGGGGAGGGGGAGGGAGAGAGAG A G ACTR3B Ensembl:ENSG00000133627 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152785449..152785591 26863196 MeRIP-seq:(Medium) rs1434680505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3764,RMVar_hsa_circ_266069,RMVar_hsa_circ_274457,RMVar_hsa_circ_336819,RMVar_hsa_circ_372393,RMVar_hsa_circ_273323,RMVar_hsa_circ_109436,RMVar_hsa_circ_249614,RMVar_hsa_circ_249615,RMVar_hsa_circ_249616,RMVar_hsa_circ_249613 82683 RMVar_ID_82683 Human_SNP_ID_345674194 m1A Human chr7 - 152804376 152804376 152804376 CTCTCGTCACCCTAACCAAGTCAGGTCCTCAGAATCACCACGCCCTCTCATTGCTGGTCGTCTGC CTCTCGTCACCCTAACCAAGTCAGGTCCTCAGCATCACCACGCCCTCTCATTGCTGGTCGTCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152804372..152804484 26863196 MeRIP-seq:(Medium) rs1042586297 Functional Loss SNV dbSNP153 33..33 33 - - - 82684 RMVar_ID_82684 Human_SNP_ID_345680450 m1A Human chr7 - 152830122 152830122 152830122 TCAGACTCAGCTCAGATGGCAGCTTCTCAAAGACTTTCTTGATCCCCTCTAATTAAATGCAATCT TCAGACTCAGCTCAGATGGCAGCTTCTCAAAGCCTTTCTTGATCCCCTCTAATTAAATGCAATCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152830108..152830356 26863196 MeRIP-seq:(Medium) rs2530930 Functional Loss SNV dbSNP153 33..33 33 - - - 82685 RMVar_ID_82685 Human_SNP_ID_345680845 m1A Human chr7 + 152831837 152831837 152831837 GGATGCGCTTGGGGCCAGATTACACAGGGCTTATGGGGAAGGCACAGGGGCCAACATTATCAACT GGATGCGCTTGGGGCCAGATTACACAGGGCTTGTGGGGAAGGCACAGGGGCCAACATTATCAACT A G ACTR3B Ensembl:ENSG00000133627 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:152831740..152831869 26863196 MeRIP-seq:(Medium) rs369993848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844121 RMVar_hsa_circ_3764,RMVar_hsa_circ_126935,RMVar_hsa_circ_330385,RMVar_hsa_circ_249622,RMVar_hsa_circ_371990,RMVar_hsa_circ_249625 82686 RMVar_ID_82686 Human_SNP_ID_345680909 m1A Human chr7 + 152832093 152832093 152832093 CACGCGGAGGCAGGACAGTGCCCGTATTGGGAAATGGCTGTAGGTGGCTCATGGAGGAAGCCGGG CACGCGGAGGCAGGACAGTGCCCGTATTGGGATATGGCTGTAGGTGGCTCATGGAGGAAGCCGGG A T ACTR3B Ensembl:ENSG00000133627 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152832054..152832145 26863196 MeRIP-seq:(Medium) rs960619812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3764,RMVar_hsa_circ_126935,RMVar_hsa_circ_330385,RMVar_hsa_circ_249622,RMVar_hsa_circ_371990,RMVar_hsa_circ_249625 82687 RMVar_ID_82687 Human_SNP_ID_345686699 m1A Human chr7 - 152854728 152854728 152854728 GAAGGAGGAGGCTGGCAGACAGCGGTCGGCACACGGATAAATGGCTTTTACTGAAGGGCCCGCGC GAAGGAGGAGGCTGGCAGACAGCGGTCGGCACGCGGATAAATGGCTTTTACTGAAGGGCCCGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152854678..152854851 26863196 MeRIP-seq:(Medium) rs755806147 Functional Loss SNV dbSNP153 33..33 33 - - - 82688 RMVar_ID_82688 Human_SNP_ID_345691672 m1A Human chr7 - 152872703 152872692 152872703 CCACCTGACCGCCCCTCCTGCCCGGCCACCAGACCACCCCTCCTGCCCGGCCACCAGACCACCCC CCACCTGACCGCCCCTCCTGCCCGGCCACCAG___________TGCCCGGCCACCAGACCACCCC AGGAGGGGTGGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152872525..152872919 26863196 MeRIP-seq:(Medium) rs1337080385 Functional Loss DEL dbSNP153 33..43 33 - - - 82689 RMVar_ID_82689 Human_SNP_ID_345691680 m1A Human chr7 - 152872705 152872705 152872705 AGCCACCTGACCGCCCCTCCTGCCCGGCCACCAGACCACCCCTCCTGCCCGGCCACCAGACCACC AGCCACCTGACCGCCCCTCCTGCCCGGCCACCTGACCACCCCTCCTGCCCGGCCACCAGACCACC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:152872605..152872851 26863196 MeRIP-seq:(Medium) rs1328292198 Functional Loss SNV dbSNP153 33..33 33 - - - 82690 RMVar_ID_82690 Human_SNP_ID_345691681 m1A Human chr7 - 152872705 152872705 152872705 AGCCACCTGACCGCCCCTCCTGCCCGGCCACCAGACCACCCCTCCTGCCCGGCCACCAGACCACC AGCCACCTGACCGCCCCTCCTGCCCGGCCACCGGACCACCCCTCCTGCCCGGCCACCAGACCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:152872605..152872851 26863196 MeRIP-seq:(Medium) rs1328292198 Functional Loss SNV dbSNP153 33..33 33 - - - 82691 RMVar_ID_82691 Human_SNP_ID_345691682 m1A Human chr7 - 152872705 152872705 152872705 AGCCACCTGACCGCCCCTCCTGCCCGGCCACCAGACCACCCCTCCTGCCCGGCCACCAGACCACC AGCCACCTGACCGCCCCTCCTGCCCGGCCACCCGACCACCCCTCCTGCCCGGCCACCAGACCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:152872605..152872851 26863196 MeRIP-seq:(Medium) rs1328292198 Functional Loss SNV dbSNP153 33..33 33 - - - 82692 RMVar_ID_82692 Human_SNP_ID_345691770 m1A Human chr7 + 152872826 152872826 152872826 GAGGGTCGGTCCGGTGGCCATGCAGGAGGGGCAGTCCGGTGGCTGGGCAGGAGGGGTGGTCCGGT GAGGGTCGGTCCGGTGGCCATGCAGGAGGGGCGGTCCGGTGGCTGGGCAGGAGGGGTGGTCCGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:152872778..152872869 26863196 MeRIP-seq:(Medium) rs911580963 Functional Loss SNV dbSNP153 33..33 33 - - - 82693 RMVar_ID_82693 Human_SNP_ID_345696716 m1A Human chr7 + 152891334 152891334 152891334 GCGTCCCCACAGCATCCCCATCGGGTGTCCCCACAGCCCATCCCCACATTATCCCCACAGTGCCC GCGTCCCCACAGCATCCCCATCGGGTGTCCCCCCAGCCCATCCCCACATTATCCCCACAGTGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:152891283..152891394 26863196 MeRIP-seq:(Medium) rs1340093112 Functional Loss SNV dbSNP153 33..33 33 - - - 82694 RMVar_ID_82694 Human_SNP_ID_346234619 m1A Human chr7 + 154966926 154966926 154966926 ACCCTCCTTTGCACCCTCCTGTCAGTTTCACCAATCACATGCCTTTGGCTGTGCTGCACTATTTG ACCCTCCTTTGCACCCTCCTGTCAGTTTCACCGATCACATGCCTTTGGCTGTGCTGCACTATTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:154966894..154967063 26863196 MeRIP-seq:(Medium) rs902298673 Functional Loss SNV dbSNP153 33..33 33 - - - 82695 RMVar_ID_82695 Human_SNP_ID_346235114 m1A Human chr7 - 154968797 154968797 154968797 GCCCATCCGCATCAGTTTTCACAGCAACAGCTACAGTTTCCACAGCAACAGTTGCATCCTCCACA GCCCATCCGCATCAGTTTTCACAGCAACAGCTGCAGTTTCCACAGCAACAGTTGCATCCTCCACA T C PAXIP1 Ensembl:ENSG00000157212 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:154968748..154968899 26863196 MeRIP-seq:(Medium) rs1317936370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17315029,Human_RBP_ID_18878899,Human_RBP_ID_22111527,Human_RBP_ID_26358531,Human_RBP_ID_27830042 RMVar_hsa_circ_116575,RMVar_hsa_circ_249648,RMVar_hsa_circ_51259,RMVar_hsa_circ_62387,RMVar_hsa_circ_373419,RMVar_hsa_circ_48410,RMVar_hsa_circ_69168,RMVar_hsa_circ_74093,RMVar_hsa_circ_249649,RMVar_hsa_circ_26707,RMVar_hsa_circ_37617,RMVar_hsa_circ_95345,RMVar_hsa_circ_86230,RMVar_hsa_circ_249652,RMVar_hsa_circ_249653,RMVar_hsa_circ_57836,RMVar_hsa_circ_287023,RMVar_hsa_circ_363914,RMVar_hsa_circ_278003,RMVar_hsa_circ_21758 82696 RMVar_ID_82696 Human_SNP_ID_346236216 m1A Human chr7 - 154973463 154973463 154973463 AGAGAGAGAAGGTCATCGGGTTTGAGGAGAATAGAAGATTTTCAAATAGGTGATTCATAGATAGG AGAGAGAGAAGGTCATCGGGTTTGAGGAGAATTGAAGATTTTCAAATAGGTGATTCATAGATAGG T A PAXIP1 Ensembl:ENSG00000157212 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:154973413..154973511 26863196 MeRIP-seq:(Medium) rs1208618865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16282650,Human_RBP_ID_24201387 RMVar_hsa_circ_116575,RMVar_hsa_circ_249648,RMVar_hsa_circ_51259,RMVar_hsa_circ_62387,RMVar_hsa_circ_48410,RMVar_hsa_circ_69168,RMVar_hsa_circ_74093,RMVar_hsa_circ_26707,RMVar_hsa_circ_95345,RMVar_hsa_circ_86230,RMVar_hsa_circ_249652,RMVar_hsa_circ_249653,RMVar_hsa_circ_287023,RMVar_hsa_circ_363914,RMVar_hsa_circ_278003,RMVar_hsa_circ_21758 82697 RMVar_ID_82697 Human_SNP_ID_346236950 m1A Human chr7 + 154976206 154976206 154976206 TCCTCCTCTTCCTCTTCCTCTTCTTCCTCTTCATAAATAATCAGACGAGGATGATAAAATGCTTC TCCTCCTCTTCCTCTTCCTCTTCTTCCTCTTCGTAAATAATCAGACGAGGATGATAAAATGCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:154976155..154976262 26863196 MeRIP-seq:(Medium) rs1426988575 Functional Loss SNV dbSNP153 33..33 33 - - - 82698 RMVar_ID_82698 Human_SNP_ID_346239637 m1A Human chr7 - 154988205 154988204 154988205 ATTCTGCATAGAGCAAGGTGGAAGGAGAAGTCAGGAGTACACAGAGGCTAGATAAGAGGAGACTG ATTCTGCATAGAGCAAGGTGGAAGGAGAAGTC_GGAGTACACAGAGGCTAGATAAGAGGAGACTG CT C PAXIP1 Ensembl:ENSG00000157212 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:154988107..154988335 26863196 MeRIP-seq:(Medium) rs1488551333 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16080471 RMVar_hsa_circ_116575,RMVar_hsa_circ_249648,RMVar_hsa_circ_51259,RMVar_hsa_circ_62387,RMVar_hsa_circ_69168,RMVar_hsa_circ_278003,RMVar_hsa_circ_249657,RMVar_hsa_circ_249655,RMVar_hsa_circ_290565,RMVar_hsa_circ_341168,RMVar_hsa_circ_271511,RMVar_hsa_circ_249656 82699 RMVar_ID_82699 Human_SNP_ID_346243471 m1A Human chr7 - 155002911 155002911 155002911 GGGCCGCCGCGATCATGTCGGACCAGGCGCCCAAAGTTCCTGAGGAGATGTTCAGGGAGGTCAAG GGGCCGCCGCGATCATGTCGGACCAGGCGCCCGAAGTTCCTGAGGAGATGTTCAGGGAGGTCAAG T C PAXIP1 Ensembl:ENSG00000157212 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155002862..155002933 26863196 MeRIP-seq:(Medium) rs1377657643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1683919,Human_RBP_ID_3073690,Human_RBP_ID_3972807,Human_RBP_ID_9404104,Human_RBP_ID_9439456,Human_RBP_ID_16080787,Human_RBP_ID_18878924 Human_Splice_Rec_941571,Human_Splice_Rec_941633,Human_Splice_Rec_941671,Human_Splice_Rec_941759 82700 RMVar_ID_82700 Human_SNP_ID_346243576 m1A Human chr7 + 155003064 155003064 155003064 CCTGCCCGCGCAGCCCGGGCCCGGTCCTGCGAATCGGGGTCCGCTCCCCCGCCCTCCGCGCCCCC CCTGCCCGCGCAGCCCGGGCCCGGTCCTGCGAGTCGGGGTCCGCTCCCCCGCCCTCCGCGCCCCC A G PAXIP1-AS1 RNACentral:URS0000D5CDC2 lincRNA exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:155002963..155003071 26863410 MeRIP-seq:(Medium) rs967173330 Functional Loss SNV dbSNP153 33..33 33 - - - 82701 RMVar_ID_82701 Human_SNP_ID_346243861 m1A Human chr7 - 155003536 155003536 155003536 CCGCACTCGCGGCCACTGCGAACAGCCGGGACACCCAATCCCACTCCGCCCAGGGCCAAGAAGCC CCGCACTCGCGGCCACTGCGAACAGCCGGGACGCCCAATCCCACTCCGCCCAGGGCCAAGAAGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155003487..155003599 26863196 MeRIP-seq:(Medium) rs1424077433 Functional Loss SNV dbSNP153 33..33 33 - - - 82702 RMVar_ID_82702 Human_SNP_ID_346243998 m1A Human chr7 + 155003896 155003896 155003896 AGCAGAGCCCGCGGTGCAGCTCCAGCCCCGGGAAGCCCCGCGCTCAACAGGTTAATACTACACAG AGCAGAGCCCGCGGTGCAGCTCCAGCCCCGGGGAGCCCCGCGCTCAACAGGTTAATACTACACAG A G PAXIP1-AS1 Ensembl:ENSG00000273344 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155003845..155003930 26863196 MeRIP-seq:(Medium) rs1463914393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22687627 82703 RMVar_ID_82703 Human_SNP_ID_346244131 m1A Human chr7 + 155004339 155004339 155004339 CGCGGTGGCTCACGCCTGTAATCCTATCCTTTAGGAGGCCGAGGTGGGCGGATTGCCTGAGTTCA CGCGGTGGCTCACGCCTGTAATCCTATCCTTTGGGAGGCCGAGGTGGGCGGATTGCCTGAGTTCA A G PAXIP1-AS1 Ensembl:ENSG00000273344 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11552216 Functional Loss SNV dbSNP153 33..33 33 - - - 82704 RMVar_ID_82704 Human_SNP_ID_346300181 m1A Human chr7 + 155206113 155206103 155206113 TGTGCCCGCGTGTCAGTGTGTCTGTGTGTGTCAGTGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT TGTGCCCGCGTGTCAGTGTGTCT__________GTGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT TGTGTGTGTCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155205979..155206267 26863196 MeRIP-seq:(Medium) rs1278702256 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_24201486 82705 RMVar_ID_82705 Human_SNP_ID_346300185 m1A Human chr7 + 155206113 155206112 155206114 TGTGCCCGCGTGTCAGTGTGTCTGTGTGTGTCAGTGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT TGTGCCCGCGTGTCAGTGTGTCTGTGTGTGTC__TGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155205979..155206267 26863196 MeRIP-seq:(Medium) rs1563463477 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24201486 82706 RMVar_ID_82706 Human_SNP_ID_346300187 m1A Human chr7 + 155206113 155206113 155206113 TGTGCCCGCGTGTCAGTGTGTCTGTGTGTGTCAGTGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT TGTGCCCGCGTGTCAGTGTGTCTGTGTGTGTCGGTGTGTGTGAGTGGTCGAGAGTGTGTCCGTAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155205979..155206267 26863196 MeRIP-seq:(Medium) rs1311132111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24201486 82707 RMVar_ID_82707 Human_SNP_ID_346300207 m1A Human chr7 - 155206128 155206128 155206128 CACTGACACATTCACATACGGACACACTCTCGACCACTCACACACACTGACACACACAGACACAC CACTGACACATTCACATACGGACACACTCTCGGCCACTCACACACACTGACACACACAGACACAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155205955..155206264 26863196 MeRIP-seq:(Medium) rs1265103335 Functional Loss SNV dbSNP153 33..33 33 - - - 82708 RMVar_ID_82708 Human_SNP_ID_346300208 m1A Human chr7 - 155206128 155206128 155206128 CACTGACACATTCACATACGGACACACTCTCGACCACTCACACACACTGACACACACAGACACAC CACTGACACATTCACATACGGACACACTCTCGCCCACTCACACACACTGACACACACAGACACAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155205955..155206264 26863196 MeRIP-seq:(Medium) rs1265103335 Functional Loss SNV dbSNP153 33..33 33 - - - 82709 RMVar_ID_82709 Human_SNP_ID_346300209 m1A Human chr7 + 155206131 155206129 155206131 TGTCTGTGTGTGTCAGTGTGTGTGAGTGGTCGAGAGTGTGTCCGTATGTGAATGTGTCAGTGTTT TGTCTGTGTGTGTCAGTGTGTGTGAGTGGTC__GAGTGTGTCCGTATGTGAATGTGTCAGTGTTT CGA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:155206030..155206171 26863196 MeRIP-seq:(Medium) rs1477998329 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_24201486 82710 RMVar_ID_82710 Human_SNP_ID_346300484 m1A Human chr7 - 155206549 155206549 155206549 TCAGGGACTTCTTTATAGCCAGGTGAGAACGGACTAAGAAGAAAAAGTTGGGAAGCAGACGCTGA TCAGGGACTTCTTTATAGCCAGGTGAGAACGGGCTAAGAAGAAAAAGTTGGGAAGCAGACGCTGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:155206539..155206666 26863196 MeRIP-seq:(Medium) rs1254543352 Functional Loss SNV dbSNP153 33..33 33 - - - 82711 RMVar_ID_82711 Human_SNP_ID_346301406 m1A Human chr7 + 155208163 155208163 155208163 GAGTGTGGGTATGAGTGTGTCTGTGTGTGGGGAATGAGTGTGTCTGTGGGGAATGGGTGTGAGTG GAGTGTGGGTATGAGTGTGTCTGTGTGTGGGGTATGAGTGTGTCTGTGGGGAATGGGTGTGAGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155207491..155209080 26863196 MeRIP-seq:(Medium) rs1309950641 Functional Loss SNV dbSNP153 33..33 33 - - - 82712 RMVar_ID_82712 Human_SNP_ID_346301563 m1A Human chr7 - 155208287 155208287 155208287 CACACACACAGACACACACCCATTCCCCACACACAGACACACTCATACACACACACCCATTCCCA CACACACACAGACACACACCCATTCCCCACACGCAGACACACTCATACACACACACCCATTCCCA T C lnc-PAXIP1-23,lnc-PAXIP1-23:2,lnc-PAXIP1-23:3 RNACentral:URS00008B806C,RNACentral:URS00008B365E,RNACentral:URS00008B3076 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155207513..155208394 26863196 MeRIP-seq:(Medium) rs1481626631 Functional Loss SNV dbSNP153 33..33 33 - - - 82713 RMVar_ID_82713 Human_SNP_ID_346301564 m1A Human chr7 - 155208287 155208287 155208287 CACACACACAGACACACACCCATTCCCCACACACAGACACACTCATACACACACACCCATTCCCA CACACACACAGACACACACCCATTCCCCACACCCAGACACACTCATACACACACACCCATTCCCA T G lnc-PAXIP1-23,lnc-PAXIP1-23:2,lnc-PAXIP1-23:3 RNACentral:URS00008B806C,RNACentral:URS00008B365E,RNACentral:URS00008B3076 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155207513..155208394 26863196 MeRIP-seq:(Medium) rs1481626631 Functional Loss SNV dbSNP153 33..33 33 - - - 82714 RMVar_ID_82714 Human_SNP_ID_346301792 m1A Human chr7 + 155208530 155208519 155208531 TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGAATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG TGTGTGTGTGTGTAGGAATGGG____________TGTGAGTGTGTGTGGGAATGGGTGTGTGTGG GTGTGTGGGGGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208480..155208613 26863196 MeRIP-seq:(Medium) rs1385955867 Functional Loss DEL dbSNP153 23..34 33 - - - 82715 RMVar_ID_82715 Human_SNP_ID_346301804 m1A Human chr7 + 155208530 155208530 155208530 TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGAATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGCATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208480..155208613 26863196 MeRIP-seq:(Medium) rs111066495 Functional Loss SNV dbSNP153 33..33 33 - - - 82716 RMVar_ID_82716 Human_SNP_ID_346301805 m1A Human chr7 + 155208530 155208530 155208530 TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGAATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGGATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208480..155208613 26863196 MeRIP-seq:(Medium) rs111066495 Functional Loss SNV dbSNP153 33..33 33 - - - 82717 RMVar_ID_82717 Human_SNP_ID_346301806 m1A Human chr7 + 155208530 155208530 155208530 TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGAATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG TGTGTGTGTGTGTAGGAATGGGTGTGTGGGGGTATGTGAGTGTGTGTGGGAATGGGTGTGTGTGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208480..155208613 26863196 MeRIP-seq:(Medium) rs111066495 Functional Loss SNV dbSNP153 33..33 33 - - - 82718 RMVar_ID_82718 Human_SNP_ID_346302073 m1A Human chr7 - 155208769 155208769 155208769 ACACATTCCCACACACACCCATTCCCCCACACACACCCATTCCCACATACATTCCCACACACTCA ACACATTCCCACACACACCCATTCCCCCACACGCACCCATTCCCACATACATTCCCACACACTCA T C lnc-PAXIP1-23,lnc-PAXIP1-23:2,lnc-PAXIP1-23:3,lnc-PAXIP1-23:4 RNACentral:URS00008B806C,RNACentral:URS00008B365E,RNACentral:URS00008B3F27,RNACentral:URS00008B8463 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:155208486..155208858 26863196 MeRIP-seq:(Medium) rs146644061 Functional Loss SNV dbSNP153 33..33 33 - - - 82719 RMVar_ID_82719 Human_SNP_ID_346302296 m1A Human chr7 + 155208965 155208965 155208965 ATGTGAGTGTGTGTGGGAATATGTGTGTGTGTATGAGTGTGTCTGTGTGTGGGAATGGGTGTGAG ATGTGAGTGTGTGTGGGAATATGTGTGTGTGTGTGAGTGTGTCTGTGTGTGGGAATGGGTGTGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208666..155209045 26863196 MeRIP-seq:(Medium) rs200372460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24201492 82720 RMVar_ID_82720 Human_SNP_ID_346302298 m1A Human chr7 + 155208968 155208968 155208968 TGAGTGTGTGTGGGAATATGTGTGTGTGTATGAGTGTGTCTGTGTGTGGGAATGGGTGTGAGTGT TGAGTGTGTGTGGGAATATGTGTGTGTGTATGCGTGTGTCTGTGTGTGGGAATGGGTGTGAGTGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155208452..155209088 26863196 MeRIP-seq:(Medium) rs1199696719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24201492 82721 RMVar_ID_82721 Human_SNP_ID_346303814 m1A Human chr7 + 155214755 155214755 155214755 GGCGTGGGAGACAGGCTGGCACTGAGGATGACAGTGGAGAGAGATCGGGCTGGGAAGAACCGGAG GGCGTGGGAGACAGGCTGGCACTGAGGATGACCGTGGAGAGAGATCGGGCTGGGAAGAACCGGAG A C AC099552.5 Ensembl:ENSG00000287865 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155214706..155214832 26863196 MeRIP-seq:(Medium) rs1040628505 Functional Loss SNV dbSNP153 33..33 33 - - - 82722 RMVar_ID_82722 Human_SNP_ID_346326101 m1A Human chr7 - 155297395 155297395 155297395 GCGGCGGGTCTCGATCGCGCGGGCCTCCCTGGAGGGGCGCGGGCTCTGGCGGCGGGGAGGCCCCT GCGGCGGGTCTCGATCGCGCGGGCCTCCCTGGTGGGGCGCGGGCTCTGGCGGCGGGGAGGCCCCT T A AC144652.1 Ensembl:ENSG00000273117 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155297356..155297614 26863196 MeRIP-seq:(Medium) rs1563027655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337549 82723 RMVar_ID_82723 Human_SNP_ID_346326374 m1A Human chr7 - 155297925 155297925 155297925 GGCCGAGAGGCGCCCGCCCGCCGGCTCTCCGAACGGAGGCGGGGCGGGGGAAAGGAGGAGTCACG GGCCGAGAGGCGCCCGCCCGCCGGCTCTCCGAGCGGAGGCGGGGCGGGGGAAAGGAGGAGTCACG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:155297876..155298029;chr7:155297876..155297950 26863196 MeRIP-seq:(Medium) rs189798439 Functional Loss SNV dbSNP153 33..33 33 - - - 82724 RMVar_ID_82724 Human_SNP_ID_346326388 m1A Human chr7 + 155297958 155297958 155297958 TCGGAGAGCCGGCGGGCGGGCGCCTCTCGGCCAGGTACGCGGCCGGCTGGGATAGGGGTCGCGGG TCGGAGAGCCGGCGGGCGGGCGCCTCTCGGCCGGGTACGCGGCCGGCTGGGATAGGGGTCGCGGG A G INSIG1 Ensembl:ENSG00000186480 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:155297851..155298026 26863410 MeRIP-seq:(Medium) rs1194741752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956842,Human_RBP_ID_5328105,Human_RBP_ID_5429314,Human_RBP_ID_9337551,Human_RBP_ID_17427222,Human_RBP_ID_22111534 Human_Splice_Rec_941807,Human_Splice_Rec_941815,Human_Splice_Rec_941817,Human_Splice_Rec_941827 RMVar_hsa_circ_101528,RMVar_hsa_circ_249659 82725 RMVar_ID_82725 Human_SNP_ID_346326572 m1A Human chr7 + 155298401 155298398 155298401 GGGGCTGGCGGCCAAGGTTGGGGAGATGATCAACGTTTCCGTGTCCGGGCCCTCCCTGCTGGCGG GGGGCTGGCGGCCAAGGTTGGGGAGATGAT___CGTTTCCGTGTCCGGGCCCTCCCTGCTGGCGG TCAA T INSIG1 Ensembl:ENSG00000186480 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:155298376..155298400 26863196 MeRIP-seq:(Medium) rs980346553 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1683930,Human_RBP_ID_4932748,Human_RBP_ID_8909636,Human_RBP_ID_9337557,Human_RBP_ID_16080800,Human_RBP_ID_18196204,Human_RBP_ID_22111535,Human_RBP_ID_22320168,Human_RBP_ID_22534371,Human_RBP_ID_24201496,Human_RBP_ID_26545115,Human_RBP_ID_26831005,Human_RBP_ID_27109123,Human_RBP_ID_27354487 Human_miRNA_ID_2689593 RMVar_hsa_circ_101528,RMVar_hsa_circ_249660,RMVar_hsa_circ_372188,RMVar_hsa_circ_249659,RMVar_hsa_circ_355020 82726 RMVar_ID_82726 Human_SNP_ID_346331564 m1A Human chr7 + 155318231 155318231 155318231 TAATCATCATCACCATCACCATCACTATCATCACCATCTCATCATCACTATCACCATCACCATCA TAATCATCATCACCATCACCATCACTATCATCGCCATCTCATCATCACTATCACCATCACCATCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155318208..155318282 26863196 MeRIP-seq:(Medium) rs1486270112 Functional Loss SNV dbSNP153 33..33 33 - - - 82727 RMVar_ID_82727 Human_SNP_ID_346374397 m1A Human chr7 - 155457762 155457740 155457762 GGCCGCCGCCCCGCTGCGGGCCGGGGCGCCCCACCGGCGTGCGGCCGCGCCCCCGCCGAGCCCCG GGCCGCCGCCCCGCTGCGGGCCGGGGCGCCCC______________________GCCGAGCCCCG CGGGGGCGCGGCCGCACGCCGGT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:155457668..155457808 26863410 MeRIP-seq:(Medium) rs1032151965 Functional Loss DEL dbSNP153 33..54 33 - - - 82728 RMVar_ID_82728 Human_SNP_ID_346374406 m1A Human chr7 - 155457762 155457762 155457762 GGCCGCCGCCCCGCTGCGGGCCGGGGCGCCCCACCGGCGTGCGGCCGCGCCCCCGCCGAGCCCCG GGCCGCCGCCCCGCTGCGGGCCGGGGCGCCCCCCCGGCGTGCGGCCGCGCCCCCGCCGAGCCCCG T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:155457668..155457808 26863410 MeRIP-seq:(Medium) rs906440612 Functional Loss SNV dbSNP153 33..33 33 - - - 82729 RMVar_ID_82729 Human_SNP_ID_346374430 m1A Human chr7 - 155457828 155457828 155457828 GGTGCCGGGCGCCCGCGGTCAGCGCGCCCGCCACCGCCCGCACGCACATGGAGGCCCCCTCCTCG GGTGCCGGGCGCCCGCGGTCAGCGCGCCCGCCGCCGCCCGCACGCACATGGAGGCCCCCTCCTCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Starvation treatment chr7:155457719..155457851;chr7:155457729..155457869 26863196,26863410 MeRIP-seq:(Medium) rs1186623751 Functional Loss SNV dbSNP153 33..33 33 - - - 82730 RMVar_ID_82730 Human_SNP_ID_346374489 m1A Human chr7 + 155457990 155457990 155457990 TGCATGCGCGCAGCTCTCGCCCCGGGCGGCCCAGGCGGCGGCGCCGGAGCCCGAGGCGGCCGGAC TGCATGCGCGCAGCTCTCGCCCCGGGCGGCCCGGGCGGCGGCGCCGGAGCCCGAGGCGGCCGGAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:155457899..155458019 26863410 MeRIP-seq:(Medium) rs1320976588 Functional Loss SNV dbSNP153 33..33 33 - - - 82731 RMVar_ID_82731 Human_SNP_ID_346374838 m1A Human chr7 + 155458779 155458779 155458779 TCGGGCTCCCGAGAGCCCCGGCAGAACCCGCCATGTGCGCCCGGCGCGGGCGGGCCGCTCCCAGC TCGGGCTCCCGAGAGCCCCGGCAGAACCCGCCGTGTGCGCCCGGCGCGGGCGGGCCGCTCCCAGC A G EN2 Ensembl:ENSG00000164778 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:155458677..155458978 26863410 MeRIP-seq:(Medium) rs1350806900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254443,Human_RBP_ID_27354545 82732 RMVar_ID_82732 Human_SNP_ID_346374839 m1A Human chr7 + 155458779 155458779 155458779 TCGGGCTCCCGAGAGCCCCGGCAGAACCCGCCATGTGCGCCCGGCGCGGGCGGGCCGCTCCCAGC TCGGGCTCCCGAGAGCCCCGGCAGAACCCGCCTTGTGCGCCCGGCGCGGGCGGGCCGCTCCCAGC A T EN2 Ensembl:ENSG00000164778 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:155458677..155458978 26863410 MeRIP-seq:(Medium) rs1350806900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254443,Human_RBP_ID_27354545 82733 RMVar_ID_82733 Human_SNP_ID_346423971 m1A Human chr7 + 155644894 155644894 155644894 GGCCCCGCGAGTGCCATGGCGGCCGCCCTGGGAGCGAGCGGAGGAGCAGGCGCCGGAGGTACGTG GGCCCCGCGAGTGCCATGGCGGCCGCCCTGGGGGCGAGCGGAGGAGCAGGCGCCGGAGGTACGTG A G RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155644845..155644937 26863196 MeRIP-seq:(Medium) rs923211690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254523,Human_RBP_ID_794535,Human_RBP_ID_953999,Human_RBP_ID_3972810,Human_RBP_ID_5404727,Human_RBP_ID_19021674,Human_RBP_ID_19137728,Human_RBP_ID_23080481,Human_RBP_ID_26358539 Human_Splice_Rec_942005,Human_Splice_Rec_942015,Human_Splice_Rec_942049 82734 RMVar_ID_82734 Human_SNP_ID_346433869 m1A Human chr7 + 155680772 155680769 155680772 TGGATCAGAATTGTATACTCAAGAGTACCCAGAAGAAGGACAGTATGAAGGCCACGAAGCTGAGT TGGATCAGAATTGTATACTCAAGAGTACCC___AGAAGGACAGTATGAAGGCCACGAAGCTGAGT CAGA C RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155680721..155680854 26863196 MeRIP-seq:(Medium) rs760521273 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_2038327,Human_RBP_ID_5622738,Human_RBP_ID_7715227,Human_RBP_ID_9404113,Human_RBP_ID_16082153,Human_RBP_ID_17540389,Human_RBP_ID_18414254,Human_RBP_ID_24201769,Human_RBP_ID_24549058,Human_RBP_ID_26357392,Human_RBP_ID_27530029,Human_RBP_ID_27830055 RMVar_hsa_circ_72846,RMVar_hsa_circ_249671,RMVar_hsa_circ_43949,RMVar_hsa_circ_287427,RMVar_hsa_circ_249669,RMVar_hsa_circ_306816,RMVar_hsa_circ_301455,RMVar_hsa_circ_273953,RMVar_hsa_circ_271746,RMVar_hsa_circ_249673,RMVar_hsa_circ_249674,RMVar_hsa_circ_249672,RMVar_hsa_circ_114504,RMVar_hsa_circ_124662,RMVar_hsa_circ_282392,RMVar_hsa_circ_318458,RMVar_hsa_circ_249670,RMVar_hsa_circ_316104,RMVar_hsa_circ_275671,RMVar_hsa_circ_120729,RMVar_hsa_circ_89341,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249679,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_249680,RMVar_hsa_circ_249678,RMVar_hsa_circ_295604,RMVar_hsa_circ_369595,RMVar_hsa_circ_127344,RMVar_hsa_circ_56717,RMVar_hsa_circ_65593,RMVar_hsa_circ_249687,RMVar_hsa_circ_249688,RMVar_hsa_circ_249690,RMVar_hsa_circ_71105,RMVar_hsa_circ_249685,RMVar_hsa_circ_374923,RMVar_hsa_circ_249689 82735 RMVar_ID_82735 Human_SNP_ID_346442152 m1A Human chr7 + 155713507 155713507 155713507 CGTGGGAATGGGGGCAGGAGGAGAGCCTGGCAAAGGAGCCGAGAGGGAGGAAGGAGGATGACGGT CGTGGGAATGGGGGCAGGAGGAGAGCCTGGCAGAGGAGCCGAGAGGGAGGAAGGAGGATGACGGT A G RBM33 Ensembl:ENSG00000184863 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155713213..155713721 26863196 MeRIP-seq:(Medium) rs1429360474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843283,Human_RBP_ID_3864444,Human_RBP_ID_22622107,Human_RBP_ID_26794853 RMVar_hsa_circ_72846,RMVar_hsa_circ_43949,RMVar_hsa_circ_124662,RMVar_hsa_circ_249670,RMVar_hsa_circ_120729,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_336683,RMVar_hsa_circ_249693,RMVar_hsa_circ_358134,RMVar_hsa_circ_363833,RMVar_hsa_circ_61000,RMVar_hsa_circ_42301,RMVar_hsa_circ_285535,RMVar_hsa_circ_72053,RMVar_hsa_circ_125145,RMVar_hsa_circ_73384,RMVar_hsa_circ_249695,RMVar_hsa_circ_126622,RMVar_hsa_circ_368148,RMVar_hsa_circ_112913,RMVar_hsa_circ_80095,RMVar_hsa_circ_82952,RMVar_hsa_circ_77184,RMVar_hsa_circ_249696,RMVar_hsa_circ_249698,RMVar_hsa_circ_249700,RMVar_hsa_circ_249701,RMVar_hsa_circ_249699,RMVar_hsa_circ_249697 82736 RMVar_ID_82736 Human_SNP_ID_346442268 m1A Human chr7 + 155714012 155714012 155714012 TCCTCGGTGGGTAGCAGGGAGCTAGAGTGGGGAGGTAGGAGGGCGTGTTGAAGGTCTGAGGAGAG TCCTCGGTGGGTAGCAGGGAGCTAGAGTGGGGTGGTAGGAGGGCGTGTTGAAGGTCTGAGGAGAG A T RBM33 Ensembl:ENSG00000184863 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr7:155713849..155714946;chr7:155713916..155714209;chr7:155713900..155714054 26863196 MeRIP-seq:(Medium) rs946972026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842354,Human_RBP_ID_7715390,Human_RBP_ID_8150740,Human_RBP_ID_9439459,Human_RBP_ID_17168545 RMVar_hsa_circ_72846,RMVar_hsa_circ_43949,RMVar_hsa_circ_124662,RMVar_hsa_circ_249670,RMVar_hsa_circ_120729,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_336683,RMVar_hsa_circ_249693,RMVar_hsa_circ_358134,RMVar_hsa_circ_363833,RMVar_hsa_circ_61000,RMVar_hsa_circ_42301,RMVar_hsa_circ_285535,RMVar_hsa_circ_72053,RMVar_hsa_circ_125145,RMVar_hsa_circ_73384,RMVar_hsa_circ_249695,RMVar_hsa_circ_126622,RMVar_hsa_circ_368148,RMVar_hsa_circ_112913,RMVar_hsa_circ_80095,RMVar_hsa_circ_82952,RMVar_hsa_circ_77184,RMVar_hsa_circ_249696,RMVar_hsa_circ_249698,RMVar_hsa_circ_249700,RMVar_hsa_circ_249701,RMVar_hsa_circ_249699,RMVar_hsa_circ_249697 82737 RMVar_ID_82737 Human_SNP_ID_346448382 m1A Human chr7 + 155737547 155737547 155737547 GTTGTTGTTCTTTAGGGCCCTCCAGAATTTCCACAGCATACACCTGGACCTGTTCCCAACAGTTT GTTGTTGTTCTTTAGGGCCCTCCAGAATTTCCTCAGCATACACCTGGACCTGTTCCCAACAGTTT A T RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155737520..155737602 26863196 MeRIP-seq:(Medium) rs1245657413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85627,Human_RBP_ID_955150,Human_RBP_ID_8662639,Human_RBP_ID_9405053,Human_RBP_ID_16083947,Human_RBP_ID_22686175,Human_RBP_ID_26132408,Human_RBP_ID_26357406 Human_Splice_Rec_942032,Human_Splice_Rec_942076,Human_Splice_Rec_942092,Human_Splice_Rec_942100 RMVar_hsa_circ_124662,RMVar_hsa_circ_120729,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_358134,RMVar_hsa_circ_363833,RMVar_hsa_circ_42301,RMVar_hsa_circ_72053,RMVar_hsa_circ_125145,RMVar_hsa_circ_126622,RMVar_hsa_circ_368148,RMVar_hsa_circ_112913,RMVar_hsa_circ_80095,RMVar_hsa_circ_82952,RMVar_hsa_circ_77184,RMVar_hsa_circ_249696,RMVar_hsa_circ_249698,RMVar_hsa_circ_249700,RMVar_hsa_circ_249701,RMVar_hsa_circ_249699,RMVar_hsa_circ_249697,RMVar_hsa_circ_249703,RMVar_hsa_circ_118858,RMVar_hsa_circ_123050,RMVar_hsa_circ_249704,RMVar_hsa_circ_25886,RMVar_hsa_circ_321738,RMVar_hsa_circ_342357,RMVar_hsa_circ_249705 82738 RMVar_ID_82738 Human_SNP_ID_346449158 m1A Human chr7 - 155739926 155739926 155739926 CGTGAGGCCGGAACTGTGGCTGAGACATCGGCATCAAAGGAGGGGGCGGGACGGACAGGTGGTGG CGTGAGGCCGGAACTGTGGCTGAGACATCGGCTTCAAAGGAGGGGGCGGGACGGACAGGTGGTGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155739877..155739972 26863196 MeRIP-seq:(Medium) rs1245061290 Functional Loss SNV dbSNP153 33..33 33 - - - 82739 RMVar_ID_82739 Human_SNP_ID_346449167 m1A Human chr7 - 155739936 155739936 155739936 GCGGTCTGTACGTGAGGCCGGAACTGTGGCTGAGACATCGGCATCAAAGGAGGGGGCGGGACGGA GCGGTCTGTACGTGAGGCCGGAACTGTGGCTGGGACATCGGCATCAAAGGAGGGGGCGGGACGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155739693..155740050 26863196 MeRIP-seq:(Medium) rs1158477095 Functional Loss SNV dbSNP153 33..33 33 - - - 82740 RMVar_ID_82740 Human_SNP_ID_346450746 m1A Human chr7 - 155745542 155745539 155745542 TTGGAGCTGATGTGGGGCCCGTCTCCACCACCACTGTTTGTCCTGTGCGTGACAGTCCTTTTCAC TTGGAGCTGATGTGGGGCCCGTCTCCACCACC___GTTTGTCCTGTGCGTGACAGTCCTTTTCAC CAGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155745493..155745580 26863196 MeRIP-seq:(Medium) rs767021856 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_249709 82741 RMVar_ID_82741 Human_SNP_ID_346450751 m1A Human chr7 - 155745542 155745542 155745542 TTGGAGCTGATGTGGGGCCCGTCTCCACCACCACTGTTTGTCCTGTGCGTGACAGTCCTTTTCAC TTGGAGCTGATGTGGGGCCCGTCTCCACCACCGCTGTTTGTCCTGTGCGTGACAGTCCTTTTCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155745493..155745580 26863196 MeRIP-seq:(Medium) rs1024594442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249709 82742 RMVar_ID_82742 Human_SNP_ID_346456758 m1A Human chr7 + 155769826 155769826 155769826 ACACTAAGCAGTGTCAGACACGGATTCCAGAAAAGCCCACGTCACAGGCTTAAAGAACAGATGTG ACACTAAGCAGTGTCAGACACGGATTCCAGAAGAGCCCACGTCACAGGCTTAAAGAACAGATGTG A G RBM33 Ensembl:ENSG00000184863 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155769780..155769903 26863196 MeRIP-seq:(Medium) rs1472790944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16085193,Human_RBP_ID_22529816,Human_RBP_ID_27109286 RMVar_hsa_circ_108904,RMVar_hsa_circ_249684,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_42301,RMVar_hsa_circ_112913,RMVar_hsa_circ_82952,RMVar_hsa_circ_249696,RMVar_hsa_circ_249697,RMVar_hsa_circ_249712,RMVar_hsa_circ_102079,RMVar_hsa_circ_249710,RMVar_hsa_circ_276061,RMVar_hsa_circ_249713,RMVar_hsa_circ_249711 82743 RMVar_ID_82743 Human_SNP_ID_346458953 m1A Human chr7 + 155778425 155778425 155778425 AGGAGTTTAGGGTGAAAAGGAGGAAGGGATGGACAGACCCAGGTGAGGAGAGGCCTGGGGATTGG AGGAGTTTAGGGTGAAAAGGAGGAAGGGATGGGCAGACCCAGGTGAGGAGAGGCCTGGGGATTGG A G RBM33 Ensembl:ENSG00000184863 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:155778375..155778618 26863196 MeRIP-seq:(Medium) rs762187855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793972,Human_RBP_ID_7715984,Human_RBP_ID_16085691,Human_RBP_ID_17169828 RMVar_hsa_circ_108904,RMVar_hsa_circ_249684,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_112913,RMVar_hsa_circ_249696 82744 RMVar_ID_82744 Human_SNP_ID_346458972 m1A Human chr7 - 155778508 155778508 155778508 CCACCGACCGGACTGGATGACCTCCCCTGATAAGCCAGTGTGTTAGAAGCAAGTTGATTATTAAC CCACCGACCGGACTGGATGACCTCCCCTGATAGGCCAGTGTGTTAGAAGCAAGTTGATTATTAAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:155778404..155778616 26863196 MeRIP-seq:(Medium) rs1563189272 Functional Loss SNV dbSNP153 33..33 33 - - - 82745 RMVar_ID_82745 Human_SNP_ID_346641773 m1A Human chr7 + 156449535 156449505 156449535 TGGTGGTGGTGGTGGTGGTGACAGTGACCACGATGGTGGTGGTGGTGATGGTAATGGTGGTAATG TGG______________________________TGGTGGTGGTGGTGATGGTAATGGTGGTAATG GTGGTGGTGGTGGTGGTGACAGTGACCACGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:156449448..156449575 26863196 MeRIP-seq:(Medium) rs1374879841 Functional Loss DEL dbSNP153 4..33 33 - - - 82746 RMVar_ID_82746 Human_SNP_ID_346641796 m1A Human chr7 + 156449535 156449535 156449535 TGGTGGTGGTGGTGGTGGTGACAGTGACCACGATGGTGGTGGTGGTGATGGTAATGGTGGTAATG TGGTGGTGGTGGTGGTGGTGACAGTGACCACGGTGGTGGTGGTGGTGATGGTAATGGTGGTAATG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:156449448..156449575 26863196 MeRIP-seq:(Medium) rs866666186 Functional Loss SNV dbSNP153 33..33 33 - - - 82747 RMVar_ID_82747 Human_SNP_ID_346723872 m1A Human chr7 - 156777819 156777819 156777819 AACAACAAAGTGGGTAATGATGTCATGTTTTCAGGTATGTGATATTGAAGGAGGAGCAGAGATAG AACAACAAAGTGGGTAATGATGTCATGTTTTCGGGTATGTGATATTGAAGGAGGAGCAGAGATAG T C LMBR1 Ensembl:ENSG00000105983 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr7:156777769..156777883;chr7:156777790..156777919 26863196 MeRIP-seq:(Medium) rs1456602922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51769,RMVar_hsa_circ_32072,RMVar_hsa_circ_19847,RMVar_hsa_circ_249725,RMVar_hsa_circ_371277,RMVar_hsa_circ_123821,RMVar_hsa_circ_249724,RMVar_hsa_circ_337120,RMVar_hsa_circ_285312,RMVar_hsa_circ_276355,RMVar_hsa_circ_249727,RMVar_hsa_circ_249728,RMVar_hsa_circ_249726,RMVar_hsa_circ_293118,RMVar_hsa_circ_37676,RMVar_hsa_circ_249736,RMVar_hsa_circ_249735,RMVar_hsa_circ_363625,RMVar_hsa_circ_346034,RMVar_hsa_circ_306523,RMVar_hsa_circ_47529,RMVar_hsa_circ_275835,RMVar_hsa_circ_249738,RMVar_hsa_circ_249743,RMVar_hsa_circ_279595,RMVar_hsa_circ_249739,RMVar_hsa_circ_118386,RMVar_hsa_circ_280006,RMVar_hsa_circ_274811,RMVar_hsa_circ_274812,RMVar_hsa_circ_249741,RMVar_hsa_circ_249742,RMVar_hsa_circ_333217,RMVar_hsa_circ_357065,RMVar_hsa_circ_249740,RMVar_hsa_circ_277690,RMVar_hsa_circ_107555,RMVar_hsa_circ_249746,RMVar_hsa_circ_81732,RMVar_hsa_circ_364794,RMVar_hsa_circ_249747,RMVar_hsa_circ_249748 82748 RMVar_ID_82748 Human_SNP_ID_346753018 m1A Human chr7 + 156893002 156893002 156893002 CGACACCTCGTCCTGCCCTTCCATCCTCCTTCATGCCCGCCGCCGCGCCGCCCGCGTCCGCGTGC CGACACCTCGTCCTGCCCTTCCATCCTCCTTCGTGCCCGCCGCCGCGCCGCCCGCGTCCGCGTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:156892951..156893175 26863196 MeRIP-seq:(Medium) rs1213665962 Functional Loss SNV dbSNP153 33..33 33 - - - 82749 RMVar_ID_82749 Human_SNP_ID_346753034 m1A Human chr7 + 156893041 156893041 156893041 CCGCCGCGCCGCCCGCGTCCGCGTGCTCCGCCACACCATCGTCCGCCCGCCGCAGGGGCTCGGAC CCGCCGCGCCGCCCGCGTCCGCGTGCTCCGCCCCACCATCGTCCGCCCGCCGCAGGGGCTCGGAC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:156892996..156893149 26863196 MeRIP-seq:(Medium) rs778961157 Functional Loss SNV dbSNP153 33..33 33 - - - 82750 RMVar_ID_82750 Human_SNP_ID_346753035 m1A Human chr7 + 156893041 156893041 156893041 CCGCCGCGCCGCCCGCGTCCGCGTGCTCCGCCACACCATCGTCCGCCCGCCGCAGGGGCTCGGAC CCGCCGCGCCGCCCGCGTCCGCGTGCTCCGCCGCACCATCGTCCGCCCGCCGCAGGGGCTCGGAC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:156892996..156893149 26863196 MeRIP-seq:(Medium) rs778961157 Functional Loss SNV dbSNP153 33..33 33 - - - 82751 RMVar_ID_82751 Human_SNP_ID_346753064 m1A Human chr7 + 156893124 156893124 156893124 AGCCGGCACGGGCCCGCGAGCCGTGTTGGAACAGGTACCGCGACCACGACACCGGCCGTCGCCTC AGCCGGCACGGGCCCGCGAGCCGTGTTGGAACGGGTACCGCGACCACGACACCGGCCGTCGCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:156892891..156893175 26863196 MeRIP-seq:(Medium) rs1278645115 Functional Loss SNV dbSNP153 33..33 33 - - - 82752 RMVar_ID_82752 Human_SNP_ID_346768508 m1A Human chr7 + 156949801 156949801 156949801 GCCCGGGCGGCTCCCAGGGACGCGTGGTCCGCATGAAGCGCAGAGGCGGGCGCGGGCCGCGCCGC GCCCGGGCGGCTCCCAGGGACGCGTGGTCCGCCTGAAGCGCAGAGGCGGGCGCGGGCCGCGCCGC A C NOM1 Ensembl:ENSG00000146909 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:156949751..156949925 26863196 MeRIP-seq:(Medium) rs948740590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956855,Human_RBP_ID_5533818,Human_RBP_ID_24202782,Human_RBP_ID_26358567,Human_RBP_ID_27831061 82753 RMVar_ID_82753 Human_SNP_ID_346771907 m1A Human chr7 - 156960879 156960879 156960879 TTCTGACGCCCATGTCCACACCCACTGCCACGATCCCAACATTTGCCACCACCTACTCCCCAGCT TTCTGACGCCCATGTCCACACCCACTGCCACGGTCCCAACATTTGCCACCACCTACTCCCCAGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:156960850..156961173 26863196 MeRIP-seq:(Medium) rs1360316671 Functional Loss SNV dbSNP153 33..33 33 - - - 82754 RMVar_ID_82754 Human_SNP_ID_346772131 m1A Human chr7 - 156961818 156961818 156961818 GCCACCCCGGCCTCTACTACGCTCCTGCTCCCACCCTGGCCCCCCGCGACCTGCTCTGGACATCC GCCACCCCGGCCTCTACTACGCTCCTGCTCCCCCCCTGGCCCCCCGCGACCTGCTCTGGACATCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:156961802..156961894;chr7:156961804..156961901 26863196 MeRIP-seq:(Medium) rs922865723 Functional Loss SNV dbSNP153 33..33 33 - - - 82755 RMVar_ID_82755 Human_SNP_ID_346784907 m1A Human chr7 - 157005192 157005192 157005192 GAGGCGCGAGTGCGTGTGAGAAGAACCGACCCACCCCGCGCAAGGGGAAGCCTCCTGTCTCCCCT GAGGCGCGAGTGCGTGTGAGAAGAACCGACCCGCCCCGCGCAAGGGGAAGCCTCCTGTCTCCCCT T C MNX1 Ensembl:ENSG00000130675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:157005141..157005259 26863196 MeRIP-seq:(Medium) rs1419981268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_680013,Human_RBP_ID_953447,Human_RBP_ID_22730354,Human_RBP_ID_24202893,Human_RBP_ID_27109660 Human_miRNA_ID_1705807 82756 RMVar_ID_82756 Human_SNP_ID_346784934 m1A Human chr7 + 157005306 157005306 157005306 AGCCCCCTGGGTCTCCCTCTCGCTGTTTCTTGAAGAGCAGGTGAGGCGCCCTTGCTTAAAAGGGA AGCCCCCTGGGTCTCCCTCTCGCTGTTTCTTGTAGAGCAGGTGAGGCGCCCTTGCTTAAAAGGGA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157005268..157005373 26863196 MeRIP-seq:(Medium) rs114585602 Functional Loss SNV dbSNP153 33..33 33 - - - 82757 RMVar_ID_82757 Human_SNP_ID_346785010 m1A Human chr7 - 157005489 157005489 157005489 AGGAGCCCCGCGGCCCAGCAGGTGCGGCGCGCACGGAGCGCCCCGGCCGGCGGCTTCTCCCGGAG AGGAGCCCCGCGGCCCAGCAGGTGCGGCGCGCTCGGAGCGCCCCGGCCGGCGGCTTCTCCCGGAG T A MNX1 Ensembl:ENSG00000130675 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:157005314..157005600 26863410 MeRIP-seq:(Medium) rs1176103169 Functional Loss SNV dbSNP153 33..33 33 - - - 82758 RMVar_ID_82758 Human_SNP_ID_346785152 m1A Human chr7 - 157005704 157005704 157005704 CGAGGAGCTGCTGGGGCCGCCAGCGCCCGGAGACAAGGGCAGCGGACGCCGCCTGCGGGACTTGA CGAGGAGCTGCTGGGGCCGCCAGCGCCCGGAGGCAAGGGCAGCGGACGCCGCCTGCGGGACTTGA T C MNX1 Ensembl:ENSG00000130675 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157005654..157005831 26863196 MeRIP-seq:(Medium) rs1177224318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4933541 82759 RMVar_ID_82759 Human_SNP_ID_346785182 m1A Human chr7 - 157005746 157005746 157005746 CGGCGGGGGCGCGGGGAAGGGCGGCGCGGAGGAGCCGGGAGCCGAGGAGCTGCTGGGGCCGCCAG CGGCGGGGGCGCGGGGAAGGGCGGCGCGGAGGTGCCGGGAGCCGAGGAGCTGCTGGGGCCGCCAG T A MNX1 Ensembl:ENSG00000130675 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:157005654..157005774 26863410 MeRIP-seq:(Medium) rs751493996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5153123,Human_RBP_ID_22731247 82760 RMVar_ID_82760 Human_SNP_ID_346786889 m1A Human chr7 - 157010569 157010569 157010569 CGGGCCCGGACGCGGGGAAGCACTCGCGTGGGAGTTTGTGCGAGCGCGGCCCGGGGCGGGGCCCG CGGGCCCGGACGCGGGGAAGCACTCGCGTGGGGGTTTGTGCGAGCGCGGCCCGGGGCGGGGCCCG T C MNX1 Ensembl:ENSG00000130675 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157010255..157010651 26863196 MeRIP-seq:(Medium) rs948447524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956081 82761 RMVar_ID_82761 Human_SNP_ID_346821139 m1A Human chr7 - 157139030 157139029 157139030 CCTGCCTCGCCTGCCCCTCATCCACGCCGGCCACAGCTCGGGCCGCTGCAGGGGCGCCCAGCGGG CCTGCCTCGCCTGCCCCTCATCCACGCCGGCC_CAGCTCGGGCCGCTGCAGGGGCGCCCAGCGGG GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:157138987..157139082;chr7:157138985..157139127 26863196 MeRIP-seq:(Medium) rs1484039829 Functional Loss DEL dbSNP153 33..33 33 - - - 82762 RMVar_ID_82762 Human_SNP_ID_346821140 m1A Human chr7 - 157139030 157139030 157139030 CCTGCCTCGCCTGCCCCTCATCCACGCCGGCCACAGCTCGGGCCGCTGCAGGGGCGCCCAGCGGG CCTGCCTCGCCTGCCCCTCATCCACGCCGGCCCCAGCTCGGGCCGCTGCAGGGGCGCCCAGCGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:157138987..157139082;chr7:157138985..157139127 26863196 MeRIP-seq:(Medium) rs1346560519 Functional Loss SNV dbSNP153 33..33 33 - - - 82763 RMVar_ID_82763 Human_SNP_ID_346821158 m1A Human chr7 - 157139076 157139076 157139076 CAGCCCTGCCCTGGGGCGGGAGGGGCGGCAATACTGGAGGGGCGGCCCTGCCTCGCCTGCCCCTC CAGCCCTGCCCTGGGGCGGGAGGGGCGGCAATGCTGGAGGGGCGGCCCTGCCTCGCCTGCCCCTC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:157138986..157139162 26863410 MeRIP-seq:(Medium) rs1210825883 Functional Loss SNV dbSNP153 33..33 33 - - - 82764 RMVar_ID_82764 Human_SNP_ID_346821159 m1A Human chr7 - 157139088 157139080 157139089 GCTGTACCCTCCCAGCCCTGCCCTGGGGCGGGAGGGGCGGCAATACTGGAGGGGCGGCCCTGCCT GCTGTACCCTCCCAGCCCTGCCCTGGGGCGG_________CAATACTGGAGGGGCGGCCCTGCCT GCCGCCCCTC G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:157138993..157139133 26863410 MeRIP-seq:(Medium) rs1424886482 Functional Loss DEL dbSNP153 32..40 33 - - - 82765 RMVar_ID_82765 Human_SNP_ID_346824671 m1A Human chr7 + 157152165 157152165 157152165 GGCCAGAATGGGGGTGGGCAAAGGGTGTAGGGAAAGTGGAAGAGAAGGCTGGGAGGAAGGTAGTC GGCCAGAATGGGGGTGGGCAAAGGGTGTAGGGGAAGTGGAAGAGAAGGCTGGGAGGAAGGTAGTC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157152130..157152366 26863196 MeRIP-seq:(Medium) rs1047032962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7717650,Human_RBP_ID_8218612,Human_RBP_ID_9440015,Human_RBP_ID_18959783 RMVar_hsa_circ_101933,RMVar_hsa_circ_126971,RMVar_hsa_circ_123177,RMVar_hsa_circ_249768,RMVar_hsa_circ_249770,RMVar_hsa_circ_84720,RMVar_hsa_circ_249771,RMVar_hsa_circ_249769 82766 RMVar_ID_82766 Human_SNP_ID_346844698 m1A Human chr7 + 157227223 157227223 157227223 TGTTTAGAGAAGAGTGAGATGTTTAACCTTGAAGGGCCTTCCAAGAGGCAGTTCTGGAGCAGCAC TGTTTAGAGAAGAGTGAGATGTTTAACCTTGACGGGCCTTCCAAGAGGCAGTTCTGGAGCAGCAC A C UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157227194..157227298 26863196 MeRIP-seq:(Medium) rs1563064956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16095397 RMVar_hsa_circ_126971,RMVar_hsa_circ_249768,RMVar_hsa_circ_361270,RMVar_hsa_circ_49063,RMVar_hsa_circ_249781,RMVar_hsa_circ_300471,RMVar_hsa_circ_278566,RMVar_hsa_circ_249783,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_20493,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_374912,RMVar_hsa_circ_249804,RMVar_hsa_circ_303297,RMVar_hsa_circ_118739,RMVar_hsa_circ_272453,RMVar_hsa_circ_249805,RMVar_hsa_circ_249807,RMVar_hsa_circ_249806,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_285680,RMVar_hsa_circ_249812,RMVar_hsa_circ_249811,RMVar_hsa_circ_339355,RMVar_hsa_circ_323490,RMVar_hsa_circ_49121,RMVar_hsa_circ_249819,RMVar_hsa_circ_249821,RMVar_hsa_circ_270812,RMVar_hsa_circ_282679,RMVar_hsa_circ_298259,RMVar_hsa_circ_274081,RMVar_hsa_circ_249823,RMVar_hsa_circ_249824,RMVar_hsa_circ_249822,RMVar_hsa_circ_94321,RMVar_hsa_circ_287286,RMVar_hsa_circ_302000,RMVar_hsa_circ_48156,RMVar_hsa_circ_249826,RMVar_hsa_circ_15269,RMVar_hsa_circ_353466 82767 RMVar_ID_82767 Human_SNP_ID_346847750 m1A Human chr7 + 157238897 157238894 157238898 ACCAGAGAAGTGGGATTTCAGGTGCCAAATAAAGACAGTGTTTGAAAGGAAGAGAAAGGTGGGTA ACCAGAGAAGTGGGATTTCAGGTGCCAAAT____ACAGTGTTTGAAAGGAAGAGAAAGGTGGGTA TAAAG T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157238766..157238923 26863196 MeRIP-seq:(Medium) rs1308721253 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_22529822,Human_RBP_ID_23297533 RMVar_hsa_circ_126971,RMVar_hsa_circ_249768,RMVar_hsa_circ_49063,RMVar_hsa_circ_300471,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_303297,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_249806,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_249811,RMVar_hsa_circ_339355,RMVar_hsa_circ_49121,RMVar_hsa_circ_270812,RMVar_hsa_circ_282679,RMVar_hsa_circ_274081,RMVar_hsa_circ_249823,RMVar_hsa_circ_249824,RMVar_hsa_circ_249822,RMVar_hsa_circ_94321,RMVar_hsa_circ_302000,RMVar_hsa_circ_48156,RMVar_hsa_circ_335014,RMVar_hsa_circ_249826,RMVar_hsa_circ_15269,RMVar_hsa_circ_372548,RMVar_hsa_circ_249828 82768 RMVar_ID_82768 Human_SNP_ID_346847751 m1A Human chr7 + 157238897 157238897 157238897 ACCAGAGAAGTGGGATTTCAGGTGCCAAATAAAGACAGTGTTTGAAAGGAAGAGAAAGGTGGGTA ACCAGAGAAGTGGGATTTCAGGTGCCAAATAAGGACAGTGTTTGAAAGGAAGAGAAAGGTGGGTA A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157238766..157238923 26863196 MeRIP-seq:(Medium) rs1163183201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22529822,Human_RBP_ID_23297533 RMVar_hsa_circ_126971,RMVar_hsa_circ_249768,RMVar_hsa_circ_49063,RMVar_hsa_circ_300471,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_303297,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_249806,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_249811,RMVar_hsa_circ_339355,RMVar_hsa_circ_49121,RMVar_hsa_circ_270812,RMVar_hsa_circ_282679,RMVar_hsa_circ_274081,RMVar_hsa_circ_249823,RMVar_hsa_circ_249824,RMVar_hsa_circ_249822,RMVar_hsa_circ_94321,RMVar_hsa_circ_302000,RMVar_hsa_circ_48156,RMVar_hsa_circ_335014,RMVar_hsa_circ_249826,RMVar_hsa_circ_15269,RMVar_hsa_circ_372548,RMVar_hsa_circ_249828 82769 RMVar_ID_82769 Human_SNP_ID_346847971 m1A Human chr7 - 157239744 157239744 157239744 TTTGCAGGGTGTGGTTCCTCTCTCCCTCAGCAATTCCACTGACTTATTTCCAGCAGCAAATACAC TTTGCAGGGTGTGGTTCCTCTCTCCCTCAGCAGTTCCACTGACTTATTTCCAGCAGCAAATACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157239694..157239865 26863196 MeRIP-seq:(Medium) rs1398628349 Functional Loss SNV dbSNP153 33..33 33 - - - 82770 RMVar_ID_82770 Human_SNP_ID_346848276 m1A Human chr7 + 157240883 157240883 157240883 TGGAGTTGAGGGACAGCCAGGATGGTAGAATGACAGTCAACTGTGTGCTACAGATGTCACCAAAA TGGAGTTGAGGGACAGCCAGGATGGTAGAATGCCAGTCAACTGTGTGCTACAGATGTCACCAAAA A C UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157240610..157241086 26863196 MeRIP-seq:(Medium) rs544679684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16095921 RMVar_hsa_circ_126971,RMVar_hsa_circ_249768,RMVar_hsa_circ_49063,RMVar_hsa_circ_300471,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_303297,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_249806,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_249811,RMVar_hsa_circ_339355,RMVar_hsa_circ_49121,RMVar_hsa_circ_270812,RMVar_hsa_circ_282679,RMVar_hsa_circ_274081,RMVar_hsa_circ_249823,RMVar_hsa_circ_249824,RMVar_hsa_circ_249822,RMVar_hsa_circ_94321,RMVar_hsa_circ_302000,RMVar_hsa_circ_48156,RMVar_hsa_circ_335014,RMVar_hsa_circ_249826,RMVar_hsa_circ_15269,RMVar_hsa_circ_372548,RMVar_hsa_circ_249828 82771 RMVar_ID_82771 Human_SNP_ID_346848277 m1A Human chr7 + 157240883 157240883 157240883 TGGAGTTGAGGGACAGCCAGGATGGTAGAATGACAGTCAACTGTGTGCTACAGATGTCACCAAAA TGGAGTTGAGGGACAGCCAGGATGGTAGAATGGCAGTCAACTGTGTGCTACAGATGTCACCAAAA A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157240610..157241086 26863196 MeRIP-seq:(Medium) rs544679684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16095921 RMVar_hsa_circ_126971,RMVar_hsa_circ_249768,RMVar_hsa_circ_49063,RMVar_hsa_circ_300471,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_303297,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_249806,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_249811,RMVar_hsa_circ_339355,RMVar_hsa_circ_49121,RMVar_hsa_circ_270812,RMVar_hsa_circ_282679,RMVar_hsa_circ_274081,RMVar_hsa_circ_249823,RMVar_hsa_circ_249824,RMVar_hsa_circ_249822,RMVar_hsa_circ_94321,RMVar_hsa_circ_302000,RMVar_hsa_circ_48156,RMVar_hsa_circ_335014,RMVar_hsa_circ_249826,RMVar_hsa_circ_15269,RMVar_hsa_circ_372548,RMVar_hsa_circ_249828 82772 RMVar_ID_82772 Human_SNP_ID_346855781 m1A Human chr7 - 157267673 157267673 157267673 TTCGCAAAAGTGTCTCGTCATAGAACTCGGGGAGCTTCAGCAGGTTCATGCAGGTGCTGGCTGTG TTCGCAAAAGTGTCTCGTCATAGAACTCGGGGGGCTTCAGCAGGTTCATGCAGGTGCTGGCTGTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:157267627..157267927 32194978 MeRIP-seq:(Medium) rs1208421014 Functional Loss SNV dbSNP153 33..33 33 - - - 82773 RMVar_ID_82773 Human_SNP_ID_346876116 m1A Human chr7 + 157336722 157336722 157336722 AATGGGCTCCTTCTGGCCCAACAATAAGTGCCATTTGGAATCTTCTCGGCCTTCTCTGTGCCTTC AATGGGCTCCTTCTGGCCCAACAATAAGTGCCCTTTGGAATCTTCTCGGCCTTCTCTGTGCCTTC A C DNAJB6 Ensembl:ENSG00000105993 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:157336671..157336784 26863196 MeRIP-seq:(Medium) rs957435048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_942889 82774 RMVar_ID_82774 Human_SNP_ID_346876403 m1A Human chr7 + 157337181 157337181 157337181 GGGTCTGTTCCGAGGGTCGGGGGAGGTCGCCTAGGGCCCCGCGCGCGCCCGGCAGACGGCGGACC GGGTCTGTTCCGAGGGTCGGGGGAGGTCGCCTGGGGCCCCGCGCGCGCCCGGCAGACGGCGGACC A G DNAJB6 Ensembl:ENSG00000105993 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:157337108..157337297 26863196 MeRIP-seq:(Medium) rs933096624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957040,Human_RBP_ID_9439467,Human_RBP_ID_18108275 RMVar_hsa_circ_126600,RMVar_hsa_circ_77582,RMVar_hsa_circ_249834,RMVar_hsa_circ_249835 82775 RMVar_ID_82775 Human_SNP_ID_346883651 m1A Human chr7 - 157355578 157355578 157355578 CACTGGAGGCTCTTATTTAAGGTCAGTAAAAAACCCACAGCACCACCCACAGACGTTTCCCAGCT CACTGGAGGCTCTTATTTAAGGTCAGTAAAAATCCCACAGCACCACCCACAGACGTTTCCCAGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:157355542..157355674;chr7:157355550..157355680 26863196 MeRIP-seq:(Medium) rs990391317 Functional Loss SNV dbSNP153 33..33 33 - - - 82776 RMVar_ID_82776 Human_SNP_ID_346883652 m1A Human chr7 - 157355578 157355578 157355578 CACTGGAGGCTCTTATTTAAGGTCAGTAAAAAACCCACAGCACCACCCACAGACGTTTCCCAGCT CACTGGAGGCTCTTATTTAAGGTCAGTAAAAAGCCCACAGCACCACCCACAGACGTTTCCCAGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:157355542..157355674;chr7:157355550..157355680 26863196 MeRIP-seq:(Medium) rs990391317 Functional Loss SNV dbSNP153 33..33 33 - - - 82777 RMVar_ID_82777 Human_SNP_ID_346887233 m1A Human chr7 + 157366505 157366505 157366505 GCCTTACCGACTTTTCTTTCAATTTTTAGCTAAGAAACGGGACATCTATGACAAATATGGCAAAG GCCTTACCGACTTTTCTTTCAATTTTTAGCTACGAAACGGGACATCTATGACAAATATGGCAAAG A C DNAJB6 Ensembl:ENSG00000105993 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157366501..157366575 26863196 MeRIP-seq:(Medium) rs1057518860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957047,Human_RBP_ID_3839437,Human_RBP_ID_7718779,Human_RBP_ID_8663271,Human_RBP_ID_16098259,Human_RBP_ID_19020326,Human_RBP_ID_22686194,Human_RBP_ID_23080228,Human_RBP_ID_24390655,Human_RBP_ID_24549072,Human_RBP_ID_26357441,Human_RBP_ID_27830097 Human_Splice_Rec_942896,Human_Splice_Rec_942897,Human_Splice_Rec_942906,Human_Splice_Rec_942907,Human_Splice_Rec_942920,Human_Splice_Rec_942921,Human_Splice_Rec_942932,Human_Splice_Rec_942933,Human_Splice_Rec_942950,Human_Splice_Rec_942951,Human_Splice_Rec_942964,Human_Splice_Rec_942965,Human_Splice_Rec_942982,Human_Splice_Rec_942983,Human_Splice_Rec_942992,Human_Splice_Rec_942993,Human_Splice_Rec_943004,Human_Splice_Rec_943005,Human_Splice_Rec_943018,Human_Splice_Rec_943024,Human_Splice_Rec_943025,Human_Splice_Rec_943034,Human_Splice_Rec_943035,Human_Splice_Rec_943044,Human_Splice_Rec_943045 Human_miRNA_ID_2534338,Human_miRNA_ID_2534339,Human_miRNA_ID_2536071,Human_miRNA_ID_2536072 Clinvar_Rec_426 RMVar_hsa_circ_68456,RMVar_hsa_circ_44995,RMVar_hsa_circ_126600,RMVar_hsa_circ_77582,RMVar_hsa_circ_249834,RMVar_hsa_circ_249835,RMVar_hsa_circ_287703,RMVar_hsa_circ_284115,RMVar_hsa_circ_249836,RMVar_hsa_circ_249837,RMVar_hsa_circ_286761,RMVar_hsa_circ_249838,RMVar_hsa_circ_23636 82778 RMVar_ID_82778 Human_SNP_ID_346887234 m1A Human chr7 + 157366505 157366505 157366505 GCCTTACCGACTTTTCTTTCAATTTTTAGCTAAGAAACGGGACATCTATGACAAATATGGCAAAG GCCTTACCGACTTTTCTTTCAATTTTTAGCTAGGAAACGGGACATCTATGACAAATATGGCAAAG A G DNAJB6 Ensembl:ENSG00000105993 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157366501..157366575 26863196 MeRIP-seq:(Medium) rs1057518860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957047,Human_RBP_ID_3839437,Human_RBP_ID_7718779,Human_RBP_ID_8663271,Human_RBP_ID_16098259,Human_RBP_ID_19020326,Human_RBP_ID_22686194,Human_RBP_ID_23080228,Human_RBP_ID_24390655,Human_RBP_ID_24549072,Human_RBP_ID_26357441,Human_RBP_ID_27830097 Human_Splice_Rec_942896,Human_Splice_Rec_942897,Human_Splice_Rec_942906,Human_Splice_Rec_942907,Human_Splice_Rec_942920,Human_Splice_Rec_942921,Human_Splice_Rec_942932,Human_Splice_Rec_942933,Human_Splice_Rec_942950,Human_Splice_Rec_942951,Human_Splice_Rec_942964,Human_Splice_Rec_942965,Human_Splice_Rec_942982,Human_Splice_Rec_942983,Human_Splice_Rec_942992,Human_Splice_Rec_942993,Human_Splice_Rec_943004,Human_Splice_Rec_943005,Human_Splice_Rec_943018,Human_Splice_Rec_943024,Human_Splice_Rec_943025,Human_Splice_Rec_943034,Human_Splice_Rec_943035,Human_Splice_Rec_943044,Human_Splice_Rec_943045 Human_miRNA_ID_2534338,Human_miRNA_ID_2534339,Human_miRNA_ID_2536071,Human_miRNA_ID_2536072 Clinvar_Rec_426 RMVar_hsa_circ_68456,RMVar_hsa_circ_44995,RMVar_hsa_circ_126600,RMVar_hsa_circ_77582,RMVar_hsa_circ_249834,RMVar_hsa_circ_249835,RMVar_hsa_circ_287703,RMVar_hsa_circ_284115,RMVar_hsa_circ_249836,RMVar_hsa_circ_249837,RMVar_hsa_circ_286761,RMVar_hsa_circ_249838,RMVar_hsa_circ_23636 82779 RMVar_ID_82779 Human_SNP_ID_346889708 m1A Human chr7 + 157372417 157372409 157372418 CAGCCCTGGGGACGTAGAGGAGCTCGGCGAGGAGTGCGAGGAGCCGCTGAGTGAGGAGGAGCACA CAGCCCTGGGGACGTAGAGGAGCTC_________TGCGAGGAGCCGCTGAGTGAGGAGGAGCACA CGGCGAGGAG C DNAJB6 Ensembl:ENSG00000105993 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr7:157372171..157372453;chr7:157372336..157372465 26863196 MeRIP-seq:(Medium) rs1468467141 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_253127,Human_RBP_ID_843990,Human_RBP_ID_7718833,Human_RBP_ID_16098427,Human_RBP_ID_22729528,Human_RBP_ID_23080739 RMVar_hsa_circ_68456,RMVar_hsa_circ_44995,RMVar_hsa_circ_108024,RMVar_hsa_circ_23636,RMVar_hsa_circ_249840 82780 RMVar_ID_82780 Human_SNP_ID_346901695 m1A Human chr7 + 157409861 157409849 157409862 CATGCGGAGAGGCCAGAACGCCCTGCCAGCCCAGCCTGCCGGCCTCCGCCCGCCGAAGCCGCCCC CATGCGGAGAGGCCAGAACGC_____________CCTGCCGGCCTCCGCCCGCCGAAGCCGCCCC CCCTGCCAGCCCAG C DNAJB6 Ensembl:ENSG00000105993 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:157409813..157409972;chr7:157409818..157409960 26863196 MeRIP-seq:(Medium) rs1487133645 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_253131,Human_RBP_ID_792995 Human_Splice_Rec_942942,Human_Splice_Rec_942974,Human_Splice_Rec_942996,Human_Splice_Rec_943054,Human_Splice_Rec_943070 RMVar_hsa_circ_40787,RMVar_hsa_circ_122886,RMVar_hsa_circ_249843 82781 RMVar_ID_82781 Human_SNP_ID_346903756 m1A Human chr7 + 157416081 157416081 157416081 AGCAGAGAGAGGAGTCGAAGAAGAAGAAGTCGACCAAAGGCAATCACTAGACCGGACTTGAGGCA AGCAGAGAGAGGAGTCGAAGAAGAAGAAGTCGTCCAAAGGCAATCACTAGACCGGACTTGAGGCA A T DNAJB6 Ensembl:ENSG00000105993 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:157415996..157416353;chr7:157416021..157416345;chr7:157415976..157416359 26863196 MeRIP-seq:(Medium) rs953132658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955181,Human_RBP_ID_3839486,Human_RBP_ID_7718972,Human_RBP_ID_16099549,Human_RBP_ID_18451439,Human_RBP_ID_26358582 Human_Splice_Rec_942944,Human_Splice_Rec_942976,Human_Splice_Rec_942998 Human_miRNA_ID_2585560,Human_miRNA_ID_3106983 RMVar_hsa_circ_115980,RMVar_hsa_circ_122886,RMVar_hsa_circ_249843,RMVar_hsa_circ_249844 82782 RMVar_ID_82782 Human_SNP_ID_347269376 m1A Human chr7 - 158609709 158609709 158609709 GCCTGAACACATCCTCACATTTCCCCTCACACACGCTCCCACTCACACACACTCCCCCCTTATAC GCCTGAACACATCCTCACATTTCCCCTCACACGCGCTCCCACTCACACACACTCCCCCCTTATAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158609658..158609758 26863196 MeRIP-seq:(Medium) rs1191308070 Functional Loss SNV dbSNP153 33..33 33 - - - 82783 RMVar_ID_82783 Human_SNP_ID_347269405 m1A Human chr7 - 158609777 158609774 158609778 ACACTCTGCCTCACACACACTCCCCCTCACAAACACTCCCTCCTCACCCACTATACTCACATACT ACACTCTGCCTCACACACACTCCCCCTCACA____CTCCCTCCTCACCCACTATACTCACATACT GTGTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:158609726..158609824 26863196 MeRIP-seq:(Medium) rs200294170 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3076623 82784 RMVar_ID_82784 Human_SNP_ID_347269569 m1A Human chr7 - 158610078 158610062 158610078 TCGCTCACACTTGCCCCTAAGACACACTCCCCACTAAAAACACTCCCCCTTTACACACATTGTCC TCGCTCACACTTGCCCCTAAGACACACTCCCC________________CTTTACACACATTGTCC GGGGGAGTGTTTTTAGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158610029..158610123 26863196 MeRIP-seq:(Medium) rs1364967906 Functional Loss DEL dbSNP153 33..48 33 - - - 82785 RMVar_ID_82785 Human_SNP_ID_347274641 m1A Human chr7 - 158632261 158632261 158632261 CTGGCAAGGAAAAGTACTCAGTGCTCTCAGCCAAAGCCGCGGCCTAGGTGGGGCTGGGGAGGACG CTGGCAAGGAAAAGTACTCAGTGCTCTCAGCCGAAGCCGCGGCCTAGGTGGGGCTGGGGAGGACG T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:158632211..158632435 26863196 MeRIP-seq:(Medium) rs186568425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16101390 82786 RMVar_ID_82786 Human_SNP_ID_347280640 m1A Human chr7 - 158655710 158655710 158655710 CAGATGGGGAGGACGGGGCCTGGTCATGAGGCAGGGAGGGGACGGGTGGTGCTGCGTGCAGGGCA CAGATGGGGAGGACGGGGCCTGGTCATGAGGCGGGGAGGGGACGGGTGGTGCTGCGTGCAGGGCA T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:158655686..158655761;chr7:158655635..158655763 26863196 MeRIP-seq:(Medium) rs1361296629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952981,Human_RBP_ID_3860933,Human_RBP_ID_5220750,Human_RBP_ID_5328113,Human_RBP_ID_5402642,Human_RBP_ID_8150745,Human_RBP_ID_8218648,Human_RBP_ID_9439105,Human_RBP_ID_18959794,Human_RBP_ID_19135670,Human_RBP_ID_21992806,Human_RBP_ID_22419111,Human_RBP_ID_22686204,Human_RBP_ID_22746767,Human_RBP_ID_24555007,Human_RBP_ID_24563037,Human_RBP_ID_26131286,Human_RBP_ID_26793736,Human_RBP_ID_27843001 RMVar_hsa_circ_363090,RMVar_hsa_circ_266499,RMVar_hsa_circ_65005,RMVar_hsa_circ_54910 82787 RMVar_ID_82787 Human_SNP_ID_347282994 m1A Human chr7 - 158664251 158664251 158664251 CGTTATTCGTCATTGCTTAAATGCCTGTATCCAGAGGGCAGTGAGAGAGCCTCCAGAGGACGAGG CGTTATTCGTCATTGCTTAAATGCCTGTATCCTGAGGGCAGTGAGAGAGCCTCCAGAGGACGAGG T A NCAPG2 Ensembl:ENSG00000146918 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:158664201..158664250 32194978 MeRIP-seq:(Medium) rs767030905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87340,Human_RBP_ID_8915216,Human_RBP_ID_9263573,Human_RBP_ID_16102741,Human_RBP_ID_18879679,Human_RBP_ID_26136587 Human_Splice_Rec_943344,Human_Splice_Rec_943345,Human_Splice_Rec_943402,Human_Splice_Rec_943403,Human_Splice_Rec_943458,Human_Splice_Rec_943459,Human_Splice_Rec_943502,Human_Splice_Rec_943503,Human_Splice_Rec_943550,Human_Splice_Rec_943551,Human_Splice_Rec_943602,Human_Splice_Rec_943603,Human_Splice_Rec_943632,Human_Splice_Rec_943633,Human_Splice_Rec_943640,Human_Splice_Rec_943641,Human_Splice_Rec_943646,Human_Splice_Rec_943647,Human_Splice_Rec_943654,Human_Splice_Rec_943655 Human_miRNA_ID_1548834 RMVar_hsa_circ_363090,RMVar_hsa_circ_266499,RMVar_hsa_circ_8257,RMVar_hsa_circ_65005,RMVar_hsa_circ_54910,RMVar_hsa_circ_48370,RMVar_hsa_circ_38456,RMVar_hsa_circ_47481,RMVar_hsa_circ_48931,RMVar_hsa_circ_8241 82788 RMVar_ID_82788 Human_SNP_ID_347282995 m1A Human chr7 - 158664251 158664251 158664251 CGTTATTCGTCATTGCTTAAATGCCTGTATCCAGAGGGCAGTGAGAGAGCCTCCAGAGGACGAGG CGTTATTCGTCATTGCTTAAATGCCTGTATCCGGAGGGCAGTGAGAGAGCCTCCAGAGGACGAGG T C NCAPG2 Ensembl:ENSG00000146918 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:158664201..158664250 32194978 MeRIP-seq:(Medium) rs767030905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87340,Human_RBP_ID_8915216,Human_RBP_ID_9263573,Human_RBP_ID_16102741,Human_RBP_ID_18879679,Human_RBP_ID_26136587 Human_Splice_Rec_943344,Human_Splice_Rec_943345,Human_Splice_Rec_943402,Human_Splice_Rec_943403,Human_Splice_Rec_943458,Human_Splice_Rec_943459,Human_Splice_Rec_943502,Human_Splice_Rec_943503,Human_Splice_Rec_943550,Human_Splice_Rec_943551,Human_Splice_Rec_943602,Human_Splice_Rec_943603,Human_Splice_Rec_943632,Human_Splice_Rec_943633,Human_Splice_Rec_943640,Human_Splice_Rec_943641,Human_Splice_Rec_943646,Human_Splice_Rec_943647,Human_Splice_Rec_943654,Human_Splice_Rec_943655 Human_miRNA_ID_1548834 RMVar_hsa_circ_363090,RMVar_hsa_circ_266499,RMVar_hsa_circ_8257,RMVar_hsa_circ_65005,RMVar_hsa_circ_54910,RMVar_hsa_circ_48370,RMVar_hsa_circ_38456,RMVar_hsa_circ_47481,RMVar_hsa_circ_48931,RMVar_hsa_circ_8241 82789 RMVar_ID_82789 Human_SNP_ID_347283427 m1A Human chr7 + 158665642 158665642 158665642 AGAACAAAAACCCACACACAAAACTCAACCTGAGGTTCCCATCTCCTGGTTCCCACCTTCCCTCC AGAACAAAAACCCACACACAAAACTCAACCTGGGGTTCCCATCTCCTGGTTCCCACCTTCCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158665639..158665755 26863196 MeRIP-seq:(Medium) rs981104074 Functional Loss SNV dbSNP153 33..33 33 - - - 82790 RMVar_ID_82790 Human_SNP_ID_347283970 m1A Human chr7 - 158667221 158667221 158667221 TGGCCCACCAGGAAGTTTGGGCGCCAGAGCAGAGGAAGAAGGCAGAACGTTTGCGTTTCAGTCCT TGGCCCACCAGGAAGTTTGGGCGCCAGAGCAGGGGAAGAAGGCAGAACGTTTGCGTTTCAGTCCT T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158667218..158667296 26863196 MeRIP-seq:(Medium) rs1003413803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860934,Human_RBP_ID_5153128,Human_RBP_ID_8219190,Human_RBP_ID_8944225,Human_RBP_ID_9439106,Human_RBP_ID_18959795,Human_RBP_ID_22529198 Human_Splice_Rec_943643,Human_Splice_Rec_943651 RMVar_hsa_circ_266499,RMVar_hsa_circ_8257,RMVar_hsa_circ_48370,RMVar_hsa_circ_47481,RMVar_hsa_circ_8241,RMVar_hsa_circ_79603,RMVar_hsa_circ_249875 82791 RMVar_ID_82791 Human_SNP_ID_347284276 m1A Human chr7 - 158667467 158667459 158667468 GTAAGGCGGGCGGAGGGACCCAGTAGTGGGTAAGGCGGGCGGAGGGACCCAGTAGTGGGTAAGGA GTAAGGCGGGCGGAGGGACCCAGTAGTGGGT_________GGAGGGACCCAGTAGTGGGTAAGGA CGCCCGCCTT C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158667421..158667515 26863196 MeRIP-seq:(Medium) rs1563539209 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_8218651,Human_RBP_ID_8237792,Human_RBP_ID_9439473 RMVar_hsa_circ_266499,RMVar_hsa_circ_8257,RMVar_hsa_circ_48370,RMVar_hsa_circ_47481,RMVar_hsa_circ_8241,RMVar_hsa_circ_79603,RMVar_hsa_circ_249875 82792 RMVar_ID_82792 Human_SNP_ID_347290622 m1A Human chr7 + 158690574 158690574 158690574 TTTAAAAAAATAAAAAGTGAGCATACTGTCTTAGTCTCCAGACTCCTCCTTAGTAACATGACAAA TTTAAAAAAATAAAAAGTGAGCATACTGTCTTGGTCTCCAGACTCCTCCTTAGTAACATGACAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:158690568..158690718 32194978 MeRIP-seq:(Medium) rs747657352 Functional Loss SNV dbSNP153 33..33 33 - - - 82793 RMVar_ID_82793 Human_SNP_ID_347291765 m1A Human chr7 - 158695681 158695681 158695681 ATGTCGTGGCAATGCCAGGCAATGACCACCCCAAGGCCATGCTGGGGAGAGGTAGAACATTTTGA ATGTCGTGGCAATGCCAGGCAATGACCACCCCTAGGCCATGCTGGGGAGAGGTAGAACATTTTGA T A NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:158695677..158695797 32194978 MeRIP-seq:(Medium) rs1563581095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16103605 RMVar_hsa_circ_33328,RMVar_hsa_circ_51414 82794 RMVar_ID_82794 Human_SNP_ID_347293945 m1A Human chr7 + 158704773 158704773 158704773 CCGTTTCCCGCGCTCGGACCAGATTCAAACGCACCCGCCGGCGCCCCAGACGGGCCCCGCCCTCC CCGTTTCCCGCGCTCGGACCAGATTCAAACGCCCCCGCCGGCGCCCCAGACGGGCCCCGCCCTCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:158704663..158704774;chr7:158704638..158704777;chr7:158704629..158704800;chr7:158704656..158704775 26863196 MeRIP-seq:(Medium) rs1036539532 Functional Loss SNV dbSNP153 33..33 33 - - - 82795 RMVar_ID_82795 Human_SNP_ID_347303885 m1A Human chr7 - 158733494 158733492 158733495 TAAGAGAATTGTCATGGTTCATAAATCACATTATGCTAATCTGAAATTTCTTACATAAAAATGAA TAAGAGAATTGTCATGGTTCATAAATCACAT___GCTAATCTGAAATTTCTTACATAAAAATGAA CATA C ESYT2 Ensembl:ENSG00000117868 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1218469413 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18879732,Human_RBP_ID_24515757,Human_RBP_ID_26552182,Human_RBP_ID_27766464 Human_miRNA_ID_1164840,Human_miRNA_ID_1198342,Human_miRNA_ID_1218884 RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,RMVar_hsa_circ_126312,RMVar_hsa_circ_97661,RMVar_hsa_circ_98920,RMVar_hsa_circ_249883,RMVar_hsa_circ_93877,RMVar_hsa_circ_249884,RMVar_hsa_circ_249882,RMVar_hsa_circ_249879,RMVar_hsa_circ_249880 82796 RMVar_ID_82796 Human_SNP_ID_347303886 m1A Human chr7 - 158733494 158733494 158733494 TAAGAGAATTGTCATGGTTCATAAATCACATTATGCTAATCTGAAATTTCTTACATAAAAATGAA TAAGAGAATTGTCATGGTTCATAAATCACATTGTGCTAATCTGAAATTTCTTACATAAAAATGAA T C ESYT2 Ensembl:ENSG00000117868 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs712192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18879732,Human_RBP_ID_24515757,Human_RBP_ID_26552182,Human_RBP_ID_27766464 Human_miRNA_ID_1164840,Human_miRNA_ID_1198342,Human_miRNA_ID_1218884 GWAS_ID_10014,GWAS_ID_10015,GWAS_ID_10016 RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,RMVar_hsa_circ_126312,RMVar_hsa_circ_97661,RMVar_hsa_circ_98920,RMVar_hsa_circ_249883,RMVar_hsa_circ_93877,RMVar_hsa_circ_249884,RMVar_hsa_circ_249882,RMVar_hsa_circ_249879,RMVar_hsa_circ_249880 82797 RMVar_ID_82797 Human_SNP_ID_347304003 m1A Human chr7 - 158733987 158733985 158733988 GGATTTCCTCTAGGATTTCGCCAGTTCCTACAACGTGCAGTAGGGCGGCGGTAGCTCTTGTGTCT GGATTTCCTCTAGGATTTCGCCAGTTCCTAC___GTGCAGTAGGGCGGCGGTAGCTCTTGTGTCT CGTT C ESYT2 Ensembl:ENSG00000117868 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:158733793..158734044 32194978 MeRIP-seq:(Medium) rs1563611035 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_84046,Human_RBP_ID_680406,Human_RBP_ID_5153130,Human_RBP_ID_8663597,Human_RBP_ID_17315532,Human_RBP_ID_17427505,Human_RBP_ID_18108752,Human_RBP_ID_18879733,Human_RBP_ID_23215707,Human_RBP_ID_24204692,Human_RBP_ID_27110139,Human_RBP_ID_27766478 RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,RMVar_hsa_circ_126312,RMVar_hsa_circ_97661,RMVar_hsa_circ_98920,RMVar_hsa_circ_249883,RMVar_hsa_circ_93877,RMVar_hsa_circ_249884,RMVar_hsa_circ_249882,RMVar_hsa_circ_249879,RMVar_hsa_circ_249880 82798 RMVar_ID_82798 Human_SNP_ID_347304005 m1A Human chr7 - 158733987 158733987 158733987 GGATTTCCTCTAGGATTTCGCCAGTTCCTACAACGTGCAGTAGGGCGGCGGTAGCTCTTGTGTCT GGATTTCCTCTAGGATTTCGCCAGTTCCTACAGCGTGCAGTAGGGCGGCGGTAGCTCTTGTGTCT T C ESYT2 Ensembl:ENSG00000117868 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:158733793..158734044 32194978 MeRIP-seq:(Medium) rs1180484149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84046,Human_RBP_ID_680406,Human_RBP_ID_5153130,Human_RBP_ID_8663597,Human_RBP_ID_17315532,Human_RBP_ID_17427505,Human_RBP_ID_18108752,Human_RBP_ID_18879733,Human_RBP_ID_23215707,Human_RBP_ID_24204692,Human_RBP_ID_27110139,Human_RBP_ID_27766478 RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,RMVar_hsa_circ_126312,RMVar_hsa_circ_97661,RMVar_hsa_circ_98920,RMVar_hsa_circ_249883,RMVar_hsa_circ_93877,RMVar_hsa_circ_249884,RMVar_hsa_circ_249882,RMVar_hsa_circ_249879,RMVar_hsa_circ_249880 82799 RMVar_ID_82799 Human_SNP_ID_347331635 m1A Human chr7 - 158829437 158829437 158829437 GCGAGCACCCAGCCCGCCTCGGCCGGGAGGGCAGCGCGGCACTGCGGGGCGATGAGCGGCGCCCG GCGAGCACCCAGCCCGCCTCGGCCGGGAGGGCGGCGCGGCACTGCGGGGCGATGAGCGGCGCCCG T C ESYT2 Ensembl:ENSG00000117868 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:158829324..158829550 26863196 MeRIP-seq:(Medium) rs1226319556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956096,Human_RBP_ID_5123160,Human_RBP_ID_8914818,Human_RBP_ID_18426661,Human_RBP_ID_18472460,Human_RBP_ID_18504516,Human_RBP_ID_22555043,Human_RBP_ID_26793748 Human_Splice_Rec_943798 82800 RMVar_ID_82800 Human_SNP_ID_347331648 m1A Human chr7 - 158829459 158829459 158829459 GGCTGAGCCGCCCGGGATCAGCGCGAGCACCCAGCCCGCCTCGGCCGGGAGGGCAGCGCGGCACT GGCTGAGCCGCCCGGGATCAGCGCGAGCACCCGGCCCGCCTCGGCCGGGAGGGCAGCGCGGCACT T C ESYT2 Ensembl:ENSG00000117868 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,untreat control;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:158829325..158829500;chr7:158829351..158829525;chr7:158829364..158829497;chr7:158829176..158829550;chr7:158829226..158829550 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1382398452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254219,Human_RBP_ID_794230,Human_RBP_ID_4956096,Human_RBP_ID_5123160,Human_RBP_ID_8914818,Human_RBP_ID_18426588,Human_RBP_ID_18472460,Human_RBP_ID_18504516,Human_RBP_ID_22555043 Human_Splice_Rec_943798 82801 RMVar_ID_82801 Human_SNP_ID_347345263 m1A Human chr7 - 158878161 158878161 158878161 CTCCTGGCTTCCCCTCCTCGCCTCCCCACATGATGCCCAGCACTCACAGTCAGCCCTCCTGGCCT CTCCTGGCTTCCCCTCCTCGCCTCCCCACATGGTGCCCAGCACTCACAGTCAGCCCTCCTGGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:158878153..158878232 26863196 MeRIP-seq:(Medium) rs1277640994 Functional Loss SNV dbSNP153 33..33 33 - - - 82802 RMVar_ID_82802 Human_SNP_ID_347345420 m1A Human chr7 + 158878466 158878466 158878466 GGGCGCCATGTGGGGTGGCCAGGAGGGCCGACAGTGAGTGCCGGGTGCCATGTGGAGGGGCCAGG GGGCGCCATGTGGGGTGGCCAGGAGGGCCGACTGTGAGTGCCGGGTGCCATGTGGAGGGGCCAGG A T WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:158878461..158878532 26863196 MeRIP-seq:(Medium) rs1333142927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24204896 RMVar_hsa_circ_1244,RMVar_hsa_circ_69985,RMVar_hsa_circ_325007,RMVar_hsa_circ_303490,RMVar_hsa_circ_308751,RMVar_hsa_circ_58027,RMVar_hsa_circ_60480,RMVar_hsa_circ_51711,RMVar_hsa_circ_18294,RMVar_hsa_circ_324452,RMVar_hsa_circ_351150,RMVar_hsa_circ_63693,RMVar_hsa_circ_249933 82803 RMVar_ID_82803 Human_SNP_ID_347354931 m1A Human chr7 + 158910893 158910893 158910893 GGCGATTGGCTGTGTCAGGCCTGTGAGCGAGGAGCGTTGGCTGTGTCAGGCCTGTGGGAGGAGTG GGCGATTGGCTGTGTCAGGCCTGTGAGCGAGGGGCGTTGGCTGTGTCAGGCCTGTGGGAGGAGTG A G WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158910774..158911070 26863196 MeRIP-seq:(Medium) rs1298371140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267534,Human_RBP_ID_793327,Human_RBP_ID_3860955,Human_RBP_ID_5657312,Human_RBP_ID_8150772,Human_RBP_ID_9338137,Human_RBP_ID_17167359,Human_RBP_ID_17315065,Human_RBP_ID_21994120,Human_RBP_ID_23080505,Human_RBP_ID_23116933,Human_RBP_ID_24204959 RMVar_hsa_circ_69877,RMVar_hsa_circ_303490,RMVar_hsa_circ_308751,RMVar_hsa_circ_51711,RMVar_hsa_circ_307793,RMVar_hsa_circ_249937,RMVar_hsa_circ_92286,RMVar_hsa_circ_249939,RMVar_hsa_circ_370989,RMVar_hsa_circ_249940,RMVar_hsa_circ_3221,RMVar_hsa_circ_249941,RMVar_hsa_circ_31893,RMVar_hsa_circ_349088,RMVar_hsa_circ_304606,RMVar_hsa_circ_125547,RMVar_hsa_circ_26733,RMVar_hsa_circ_319362,RMVar_hsa_circ_338481,RMVar_hsa_circ_369283,RMVar_hsa_circ_266269,RMVar_hsa_circ_15023,RMVar_hsa_circ_249943,RMVar_hsa_circ_249944,RMVar_hsa_circ_249945 82804 RMVar_ID_82804 Human_SNP_ID_347357702 m1A Human chr7 + 158917404 158917404 158917404 GTCCTCCACACTCCACCCTCTGCCTCTCACTAAACACCTCCTGTCCTCCACACTCCACCCTCCGC GTCCTCCACACTCCACCCTCTGCCTCTCACTATACACCTCCTGTCCTCCACACTCCACCCTCCGC A T WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:158917316..158917403 26863410 MeRIP-seq:(Medium) rs1431553800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303490,RMVar_hsa_circ_308751,RMVar_hsa_circ_307793,RMVar_hsa_circ_249937,RMVar_hsa_circ_92286,RMVar_hsa_circ_249939,RMVar_hsa_circ_370989,RMVar_hsa_circ_249940,RMVar_hsa_circ_35547,RMVar_hsa_circ_3221,RMVar_hsa_circ_249941,RMVar_hsa_circ_31893,RMVar_hsa_circ_349088,RMVar_hsa_circ_304606,RMVar_hsa_circ_125547,RMVar_hsa_circ_26733,RMVar_hsa_circ_319362,RMVar_hsa_circ_338481,RMVar_hsa_circ_369283,RMVar_hsa_circ_266269,RMVar_hsa_circ_15023,RMVar_hsa_circ_249943,RMVar_hsa_circ_249944,RMVar_hsa_circ_249945,RMVar_hsa_circ_271451,RMVar_hsa_circ_339022,RMVar_hsa_circ_96989,RMVar_hsa_circ_2073,RMVar_hsa_circ_249947,RMVar_hsa_circ_6782,RMVar_hsa_circ_249948,RMVar_hsa_circ_249946,RMVar_hsa_circ_249949,RMVar_hsa_circ_328087,RMVar_hsa_circ_377872,RMVar_hsa_circ_101236 82805 RMVar_ID_82805 Human_SNP_ID_347362118 m1A Human chr7 + 158932322 158932322 158932322 ATGGAGTGCAGTGGGGACATCTTGAGGAGGCAAAGACTGAGCCAGGCCTTTGAGGTGGAGTTAGA ATGGAGTGCAGTGGGGACATCTTGAGGAGGCAGAGACTGAGCCAGGCCTTTGAGGTGGAGTTAGA A G WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158932282..158932428 26863196 MeRIP-seq:(Medium) rs1267129656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26733,RMVar_hsa_circ_319362,RMVar_hsa_circ_338481,RMVar_hsa_circ_249944,RMVar_hsa_circ_249945,RMVar_hsa_circ_96989,RMVar_hsa_circ_249948,RMVar_hsa_circ_57043,RMVar_hsa_circ_79238,RMVar_hsa_circ_249952 82806 RMVar_ID_82806 Human_SNP_ID_347362296 m1A Human chr7 - 158932988 158932988 158932988 CTCCTGGGCATCTCCACAGGCACCACAAGCTCAGCCTGTCCTCACTGGAACACACTGGGCTGCTC CTCCTGGGCATCTCCACAGGCACCACAAGCTCCGCCTGTCCTCACTGGAACACACTGGGCTGCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158932966..158933145 26863196 MeRIP-seq:(Medium) rs920783855 Functional Loss SNV dbSNP153 33..33 33 - - - 82807 RMVar_ID_82807 Human_SNP_ID_347365086 m1A Human chr7 + 158943402 158943402 158943402 TCCCTCCCTGGTGGGCAAGAAAGACAATGAGCAGAGTGAACGAGGGGGTCCCGAAATGTGCTGGA TCCCTCCCTGGTGGGCAAGAAAGACAATGAGCGGAGTGAACGAGGGGGTCCCGAAATGTGCTGGA A G WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158943393..158943576 26863196 MeRIP-seq:(Medium) rs1026976993 Functional Loss SNV dbSNP153 33..33 33 - - - 82808 RMVar_ID_82808 Human_SNP_ID_347369316 m1A Human chr7 + 158958084 158958080 158958085 GTGTGGTCTGCACCTGCCCGTCAGCCACAGACACGCCCCAGGTCGTGGAGAGGGTGAGGTCTGCA GTGTGGTCTGCACCTGCCCGTCAGCCACA_____GCCCCAGGTCGTGGAGAGGGTGAGGTCTGCA AGACAC A lnc-WDR60-9 RNACentral:URS00008B5F7C lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158958036..158958121 26863196 MeRIP-seq:(Medium) rs1259989436 Functional Loss DEL dbSNP153 30..34 33 - - - 82809 RMVar_ID_82809 Human_SNP_ID_347373363 m1A Human chr7 - 158973446 158973446 158973446 ACCTGGGCCACGGACGCGCCGCGCCCTCGGGGAGCCGGCTCCGGAGGCCTCTCTCTTCCTCCTCC ACCTGGGCCACGGACGCGCCGCGCCCTCGGGGGGCCGGCTCCGGAGGCCTCTCTCTTCCTCCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:158973399..158973668 26863196 MeRIP-seq:(Medium) rs1027858413 Functional Loss SNV dbSNP153 33..33 33 - - - 82810 RMVar_ID_82810 Human_SNP_ID_347373428 m1A Human chr7 - 158973586 158973586 158973586 CGCTGAGCTCACAGGCTTCTAGGCACCTTCGGAGGCCGCTGAAGAGCGGGGGTGGCGCGAGCTGG CGCTGAGCTCACAGGCTTCTAGGCACCTTCGGTGGCCGCTGAAGAGCGGGGGTGGCGCGAGCTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:158973535..158973675 26863196 MeRIP-seq:(Medium) rs1007398627 Functional Loss SNV dbSNP153 33..33 33 - - - 82811 RMVar_ID_82811 Human_SNP_ID_347373497 m1A Human chr7 - 158973747 158973746 158973747 CACACATCTCCATCTGAGATGCAGAAACGCTAACCGGGTCCCTGCCACACGTCAAACGTCGGCGC CACACATCTCCATCTGAGATGCAGAAACGCTAGTCGGGTCCCTGCCACACGTCAAACGTCGGCGC GT AC - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:158973413..158973800 26863196 MeRIP-seq:(Medium) rs386720399 Functional Loss MNV dbSNP153 33..34 33 - - - 82812 RMVar_ID_82812 Human_SNP_ID_347373498 m1A Human chr7 - 158973747 158973747 158973747 CACACATCTCCATCTGAGATGCAGAAACGCTAACCGGGTCCCTGCCACACGTCAAACGTCGGCGC CACACATCTCCATCTGAGATGCAGAAACGCTAGCCGGGTCCCTGCCACACGTCAAACGTCGGCGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:158973413..158973800 26863196 MeRIP-seq:(Medium) rs2527220 Functional Loss SNV dbSNP153 33..33 33 - - - 82813 RMVar_ID_82813 Human_SNP_ID_347373707 m1A Human chr7 + 158974078 158974074 158974079 CCAGGCCCCCCACCCGCCTCTCTGTGCCCCCCATCCTTGCACCCCGCGCTGTCCCCGGCGGTCTG CCAGGCCCCCCACCCGCCTCTCTGTGCCC_____CCTTGCACCCCGCGCTGTCCCCGGCGGTCTG CCCCAT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:158974053..158974191 26863196 MeRIP-seq:(Medium) rs1233563881 Functional Loss DEL dbSNP153 30..34 33 - - - 82814 RMVar_ID_82814 Human_SNP_ID_347373854 m1A Human chr7 + 158974384 158974384 158974384 GATTCTGGAAGGTTCCAGAGGGTGTGCCGCCGAGGCCCTGCGAGAGGGCGTTCCCTGGGGAGAAC GATTCTGGAAGGTTCCAGAGGGTGTGCCGCCGTGGCCCTGCGAGAGGGCGTTCCCTGGGGAGAAC A T lnc-WDR60-3,lnc-WDR60-3:2 RNACentral:URS00008BE388,RNACentral:URS00008C144D lincRNA,lincRNA exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:158974299..158974425 26863196 MeRIP-seq:(Medium) rs958223349 Functional Loss SNV dbSNP153 33..33 33 - - - 82815 RMVar_ID_82815 Human_SNP_ID_347379308 m1A Human chr7 - 158992851 158992851 158992851 CAGCGCTGTCCCCCCGACAGAGGAGCTACCCCAGTCTCAGCTCTCAGCGCTGTCCCCGACAACGG CAGCGCTGTCCCCCCGACAGAGGAGCTACCCCTGTCTCAGCTCTCAGCGCTGTCCCCGACAACGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:158992814..158992956 26863196 MeRIP-seq:(Medium) rs1341315814 Functional Loss SNV dbSNP153 33..33 33 - - - 82816 RMVar_ID_82816 Human_SNP_ID_347379331 m1A Human chr7 + 158992900 158992898 158992900 CGGGGGGACAGCGCTGAGAGTGAGACTGGGGCAGCTCCTCCGTCGTCGGGGACAGCGCTGAGAGC CGGGGGGACAGCGCTGAGAGTGAGACTGGGG__GCTCCTCCGTCGTCGGGGACAGCGCTGAGAGC GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158992806..158993080 26863196 MeRIP-seq:(Medium) rs1441511639 Functional Loss DEL dbSNP153 32..33 33 - - - 82817 RMVar_ID_82817 Human_SNP_ID_347379333 m1A Human chr7 + 158992900 158992900 158992900 CGGGGGGACAGCGCTGAGAGTGAGACTGGGGCAGCTCCTCCGTCGTCGGGGACAGCGCTGAGAGC CGGGGGGACAGCGCTGAGAGTGAGACTGGGGCGGCTCCTCCGTCGTCGGGGACAGCGCTGAGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:158992806..158993080 26863196 MeRIP-seq:(Medium) rs1289746485 Functional Loss SNV dbSNP153 33..33 33 - - - 82818 RMVar_ID_82818 Human_SNP_ID_347385953 m1A Human chr7 - 159017982 159017982 159017982 GCTGAGACACACTGTAGTGATGACACAGACACAGTGGAGGGGATGAGATTGAAGCATAAAGGGGA GCTGAGACACACTGTAGTGATGACACAGACACGGTGGAGGGGATGAGATTGAAGCATAAAGGGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:159017931..159018053 26863196 MeRIP-seq:(Medium) rs781665748 Functional Loss SNV dbSNP153 33..33 33 - - - 82819 RMVar_ID_82819 Human_SNP_ID_347386269 m1A Human chr7 - 159018694 159018693 159018694 ACAATGCGGGGAGGTGAGACAGAGACACAATGAGGGGTGAGACTGAGACATAATGGGGAGTTGGG ACAATGCGGGGAGGTGAGACAGAGACACAATG_GGGGTGAGACTGAGACATAATGGGGAGTTGGG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:159018648..159018823 26863196 MeRIP-seq:(Medium) rs1445050331 Functional Loss DEL dbSNP153 33..33 33 - - - 82820 RMVar_ID_82820 Human_SNP_ID_347386270 m1A Human chr7 - 159018694 159018694 159018694 ACAATGCGGGGAGGTGAGACAGAGACACAATGAGGGGTGAGACTGAGACATAATGGGGAGTTGGG ACAATGCGGGGAGGTGAGACAGAGACACAATGGGGGGTGAGACTGAGACATAATGGGGAGTTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:159018648..159018823 26863196 MeRIP-seq:(Medium) rs1408673252 Functional Loss SNV dbSNP153 33..33 33 - - - 82821 RMVar_ID_82821 Human_SNP_ID_347386275 m1A Human chr7 - 159018706 159018706 159018706 TGAGACAGAGACACAATGCGGGGAGGTGAGACAGAGACACAATGAGGGGTGAGACTGAGACATAA TGAGACAGAGACACAATGCGGGGAGGTGAGACTGAGACACAATGAGGGGTGAGACTGAGACATAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:159018667..159018963 26863196 MeRIP-seq:(Medium) rs1161423605 Functional Loss SNV dbSNP153 33..33 33 - - - 82822 RMVar_ID_82822 Human_SNP_ID_347386297 m1A Human chr7 + 159018745 159018745 159018745 CCTCCCCGCATTGTGTCTCTGTCTCACCCCCCATTGTGTCTGTCTCAACTCCCCATTGTGTCTCT CCTCCCCGCATTGTGTCTCTGTCTCACCCCCCCTTGTGTCTGTCTCAACTCCCCATTGTGTCTCT A C LINC00689 Ensembl:ENSG00000231419 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:159018695..159018827 26863196 MeRIP-seq:(Medium) rs1346644728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249953,RMVar_hsa_circ_76745 82823 RMVar_ID_82823 Human_SNP_ID_347386298 m1A Human chr7 - 159018747 159018746 159018748 ACAGAGACACAATGGGGAGTTGAGACAGACACAATGGGGGGTGAGACAGAGACACAATGCGGGGA ACAGAGACACAATGGGGAGTTGAGACAGACA__ATGGGGGGTGAGACAGAGACACAATGCGGGGA TTG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:159018697..159018770 26863196 MeRIP-seq:(Medium) rs1409766652 Functional Loss DEL dbSNP153 32..33 33 - - - 82824 RMVar_ID_82824 Human_SNP_ID_347389132 m1A Human chr7 + 159028798 159028798 159028798 GGGCACCTGGCCTGGGCCGTTTACTCCCCAGTATCCGTCTGTGATGGATCCTCTGCGGCCCCCAG GGGCACCTGGCCTGGGCCGTTTACTCCCCAGTGTCCGTCTGTGATGGATCCTCTGCGGCCCCCAG A G LINC00689 Ensembl:ENSG00000231419 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:159028747..159028866 26863196 MeRIP-seq:(Medium) rs888897383 Functional Loss SNV dbSNP153 33..33 33 - - - 82825 RMVar_ID_82825 Human_SNP_ID_347392806 m1A Human chr7 - 159040807 159040807 159040807 GCCAAGCTGGGTCTTCCCTCTCGCTGTCCTCTAAAGAACGCTCAGGCTTTGAATAAACAAGTCAG GCCAAGCTGGGTCTTCCCTCTCGCTGTCCTCTGAAGAACGCTCAGGCTTTGAATAAACAAGTCAG T C VIPR2 Ensembl:ENSG00000106018 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:159040796..159040883 26863196 MeRIP-seq:(Medium) rs1407672707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266414 82826 RMVar_ID_82826 Human_SNP_ID_347392815 m1A Human chr7 - 159040843 159040843 159040843 ACAGGAGGGAGGGGAGATGCCTGAGGCCAGAGAGGAGCCAAGCTGGGTCTTCCCTCTCGCTGTCC ACAGGAGGGAGGGGAGATGCCTGAGGCCAGAGGGGAGCCAAGCTGGGTCTTCCCTCTCGCTGTCC T C VIPR2 Ensembl:ENSG00000106018 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:159040802..159040932 26863196 MeRIP-seq:(Medium) rs748306402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266414 82827 RMVar_ID_82827 Human_SNP_ID_347397404 m1A Human chr7 - 159060479 159060479 159060479 AGTTATGGATAAGTGAGGTGAATATGGTGGGTAAGCGAAGTGAGTATGGGTTAGATGAATTGAGA AGTTATGGATAAGTGAGGTGAATATGGTGGGTGAGCGAAGTGAGTATGGGTTAGATGAATTGAGA T C VIPR2 Ensembl:ENSG00000106018 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:159059637..159060786 26863196 MeRIP-seq:(Medium) rs1423337111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97235,RMVar_hsa_circ_249955 82828 RMVar_ID_82828 Human_SNP_ID_347420180 m1A Human chr7 + 159144337 159144337 159144337 TACAGGGAGGGACCGAGAGGCATCTGCGGCCAACGCCAACCCCGATCTCCCCGTGAAACGCGCAG TACAGGGAGGGACCGAGAGGCATCTGCGGCCAGCGCCAACCCCGATCTCCCCGTGAAACGCGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:159144331..159144615 26863196 MeRIP-seq:(Medium) rs1240791436 Functional Loss SNV dbSNP153 33..33 33 - - - 82829 RMVar_ID_82829 Human_SNP_ID_256082499 m1A Human chr5 - 150004854 150004854 150004854 CAGTTACCTCAGTACCATCATATGATGCGTCCATGGCTAAAGGAAAGGAAAGTCAAAATAAAGTT CAGTTACCTCAGTACCATCATATGATGCGTCCTTGGCTAAAGGAAAGGAAAGTCAAAATAAAGTT T A L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150004851..150004875 32194978 MeRIP-seq:(Medium) rs1413022020 Functional Loss SNV dbSNP153 33..33 33 - - - 82830 RMVar_ID_82830 Human_SNP_ID_256082500 m1A Human chr5 - 150004854 150004854 150004854 CAGTTACCTCAGTACCATCATATGATGCGTCCATGGCTAAAGGAAAGGAAAGTCAAAATAAAGTT CAGTTACCTCAGTACCATCATATGATGCGTCCGTGGCTAAAGGAAAGGAAAGTCAAAATAAAGTT T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150004851..150004875 32194978 MeRIP-seq:(Medium) rs1413022020 Functional Loss SNV dbSNP153 33..33 33 - - - 82831 RMVar_ID_82831 Human_SNP_ID_256088129 m1A Human chr5 - 150028188 150028188 150028188 GCAACCACTTGTCTCTTATCTACCTATAACCTATAAGTCCCCTCCCTGCTTTGAGTCTTCCTGCC GCAACCACTTGTCTCTTATCTACCTATAACCTGTAAGTCCCCTCCCTGCTTTGAGTCTTCCTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150028139..150028330 26863196 MeRIP-seq:(Medium) rs946743233 Functional Loss SNV dbSNP153 33..33 33 - - - 82832 RMVar_ID_82832 Human_SNP_ID_256091147 m1A Human chr5 - 150040856 150040856 150040856 AACTTTTACCTGTCTGCTCCTGCACCGACTTCAGAACAACATTGATGGACACTCTGGGGTCCTCT AACTTTTACCTGTCTGCTCCTGCACCGACTTCTGAACAACATTGATGGACACTCTGGGGTCCTCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150040805..150040913 26863196 MeRIP-seq:(Medium) rs1283158625 Functional Loss SNV dbSNP153 33..33 33 - - - 82833 RMVar_ID_82833 Human_SNP_ID_256093842 m1A Human chr5 + 150051827 150051827 150051827 AGCACCCAGTCACCAAGACTGCCACGCGGCGCATCGTCCATGCAGGCCTACAGCCCAATCCTGGT AGCACCCAGTCACCAAGACTGCCACGCGGCGCGTCGTCCATGCAGGCCTACAGCCCAATCCTGGT A G HMGXB3 Ensembl:ENSG00000113716 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150051776..150051974 26863196 MeRIP-seq:(Medium) rs912635132 Functional Loss SNV dbSNP153 33..33 33 - - - 82834 RMVar_ID_82834 Human_SNP_ID_256093871 m1A Human chr5 + 150051876 150051876 150051876 ACAGCCCAATCCTGGTGACCCCAGTGCTGGGCACCACTCCTTGGCCCTGTGCCCTGAATTGGCAC ACAGCCCAATCCTGGTGACCCCAGTGCTGGGCGCCACTCCTTGGCCCTGTGCCCTGAATTGGCAC A G HMGXB3 Ensembl:ENSG00000113716 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150051826..150051900 32194978 MeRIP-seq:(Medium) rs1330069785 Functional Loss SNV dbSNP153 33..33 33 - - - 82835 RMVar_ID_82835 Human_SNP_ID_256094159 m1A Human chr5 - 150052482 150052482 150052482 TGACCCACACCGCAGGCCCCACGGAACCCACCAGCTACGAGCCTTTCCCTCAGCCTCCCCTCCAT TGACCCACACCGCAGGCCCCACGGAACCCACCGGCTACGAGCCTTTCCCTCAGCCTCCCCTCCAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150052433..150052566 26863196 MeRIP-seq:(Medium) rs929033812 Functional Loss SNV dbSNP153 33..33 33 - - - 82836 RMVar_ID_82836 Human_SNP_ID_256094177 m1A Human chr5 - 150052508 150052508 150052508 CCTTAGCCCACCCAGGACCTCCACCCTGACCCACACCGCAGGCCCCACGGAACCCACCAGCTACG CCTTAGCCCACCCAGGACCTCCACCCTGACCCGCACCGCAGGCCCCACGGAACCCACCAGCTACG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:150052393..150052550 26863196 MeRIP-seq:(Medium) rs1401825206 Functional Loss SNV dbSNP153 33..33 33 - - - 82837 RMVar_ID_82837 Human_SNP_ID_256110813 m1A Human chr5 - 150113361 150113358 150113362 ATGATCAGGCCCCAGGTAGGAGAAGGGCAGACAGAGTGTCCAAAAGCGTGAGAGCACGAAGTGAG ATGATCAGGCCCCAGGTAGGAGAAGGGCAGA____GTGTCCAAAAGCGTGAGAGCACGAAGTGAG CTCTG C CSF1R Ensembl:ENSG00000182578 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150113266..150113398 26863196 MeRIP-seq:(Medium) rs1296009321 Functional Loss DEL dbSNP153 32..35 33 - - - 82838 RMVar_ID_82838 Human_SNP_ID_256114033 m1A Human chr5 - 150124339 150124339 150124339 ATTTTCCTCAGCCACAGCCCGCAGCAGTGAGAAGCAAGCCCTTATGTCGGAGCTGAAGATCATGA ATTTTCCTCAGCCACAGCCCGCAGCAGTGAGAGGCAAGCCCTTATGTCGGAGCTGAAGATCATGA T C PDGFRB Ensembl:ENSG00000113721 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150124192..150124350 26863196 MeRIP-seq:(Medium) rs1362685432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_709358,Human_Splice_Rec_709359,Human_Splice_Rec_709402,Human_Splice_Rec_709403 RMVar_hsa_circ_128012,RMVar_hsa_circ_85014,RMVar_hsa_circ_26715,RMVar_hsa_circ_94718,RMVar_hsa_circ_235433,RMVar_hsa_circ_235434,RMVar_hsa_circ_235436,RMVar_hsa_circ_90764,RMVar_hsa_circ_235435,RMVar_hsa_circ_44908 82839 RMVar_ID_82839 Human_SNP_ID_256150231 m1A Human chr5 + 150263557 150263557 150263557 TTACACAGACACACATTCACACACACTCCAACACTGTCACATACACACACACATACATGCATACA TTACACAGACACACATTCACACACACTCCAACGCTGTCACATACACACACACATACATGCATACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150263545..150263667 26863196 MeRIP-seq:(Medium) rs1316749181 Functional Loss SNV dbSNP153 33..33 33 - - - 82840 RMVar_ID_82840 Human_SNP_ID_256173097 m1A Human chr5 - 150357739 150357739 150357739 CCCGCCGCTTCCTGGCCTCGGCCATACCCGCGACCCCCGGCCGGCCGGCTACCTGCACGCCCCGC CCCGCCGCTTCCTGGCCTCGGCCATACCCGCGCCCCCCGGCCGGCCGGCTACCTGCACGCCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:150357676..150357905;chr5:150357651..150364200;chr5:150357651..150357906 26863196 MeRIP-seq:(Medium) rs879085626 Functional Loss SNV dbSNP153 33..33 33 - - - 82841 RMVar_ID_82841 Human_SNP_ID_256174185 m1A Human chr5 + 150361871 150361871 150361871 GGTGGACAGTACAGATGGGGCTAGGTCATCGCATGGATAGCCATGCATGGGCTGGTTATCCATGG GGTGGACAGTACAGATGGGGCTAGGTCATCGCGTGGATAGCCATGCATGGGCTGGTTATCCATGG A G TCOF1 Ensembl:ENSG00000070814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150361867..150362040 26863196 MeRIP-seq:(Medium) rs968003483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28334,RMVar_hsa_circ_311692,RMVar_hsa_circ_235450 82842 RMVar_ID_82842 Human_SNP_ID_256174186 m1A Human chr5 + 150361871 150361871 150361871 GGTGGACAGTACAGATGGGGCTAGGTCATCGCATGGATAGCCATGCATGGGCTGGTTATCCATGG GGTGGACAGTACAGATGGGGCTAGGTCATCGCTTGGATAGCCATGCATGGGCTGGTTATCCATGG A T TCOF1 Ensembl:ENSG00000070814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150361867..150362040 26863196 MeRIP-seq:(Medium) rs968003483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28334,RMVar_hsa_circ_311692,RMVar_hsa_circ_235450 82843 RMVar_ID_82843 Human_SNP_ID_256176743 m1A Human chr5 + 150372125 150372125 150372125 GGGAAGGTGGGGGATGTGACACCCCAGGTCAAAGGAGGGGCCCTGCCCCCAGCCAAGAGGGCCAA GGGAAGGTGGGGGATGTGACACCCCAGGTCAAGGGAGGGGCCCTGCCCCCAGCCAAGAGGGCCAA A G TCOF1 Ensembl:ENSG00000070814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150372076..150372257 26863196 MeRIP-seq:(Medium) rs756393850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73748,Human_RBP_ID_943860,Human_RBP_ID_3968353,Human_RBP_ID_8893777,Human_RBP_ID_18195130,Human_RBP_ID_24548217,Human_RBP_ID_27826022 RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_119381,RMVar_hsa_circ_235452,RMVar_hsa_circ_311773,RMVar_hsa_circ_235453 82844 RMVar_ID_82844 Human_SNP_ID_256176773 m1A Human chr5 + 150372190 150372190 150372190 GAAGCCAGAAGAGGAGTCAGAGAGTAGTGAGGAGGGATCTGAAAGTGAGGAGGAGGCCCCTGCAG GAAGCCAGAAGAGGAGTCAGAGAGTAGTGAGGTGGGATCTGAAAGTGAGGAGGAGGCCCCTGCAG A T TCOF1 Ensembl:ENSG00000070814 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150372071..150372250 26863196 MeRIP-seq:(Medium) rs769498945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73748,Human_RBP_ID_838606,Human_RBP_ID_3967555,Human_RBP_ID_4817315,Human_RBP_ID_7405548,Human_RBP_ID_15351079,Human_RBP_ID_18195255,Human_RBP_ID_18413619,Human_RBP_ID_23050441,Human_RBP_ID_24548217,Human_RBP_ID_26351593,Human_RBP_ID_27826022 Human_Splice_Rec_709991,Human_Splice_Rec_710137,Human_Splice_Rec_710201,Human_Splice_Rec_710235,Human_Splice_Rec_710283,Human_Splice_Rec_710315,Human_Splice_Rec_710363,Human_Splice_Rec_710411,Human_Splice_Rec_710481,Human_Splice_Rec_710493 RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_119381,RMVar_hsa_circ_235452,RMVar_hsa_circ_311773,RMVar_hsa_circ_235453 82845 RMVar_ID_82845 Human_SNP_ID_256177555 m1A Human chr5 + 150374792 150374750 150374792 CTCGCAGAGCAGCAGCGAGGAATCGGACAGTGAGGAGGAGGCGCCTGCTCAGGTGAGGCAGAGGG _________________________________GGAGGAGGCGCCTGCTCAGGTGAGGCAGAGGG GGGAGGAGGACTCGCAGAGCAGCAGCGAGGAATCGGACAGTGA G TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:150374371..150374852 32194978 MeRIP-seq:(Medium) rs1388920258 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_249809,Human_RBP_ID_945365,Human_RBP_ID_7405562,Human_RBP_ID_8886598,Human_RBP_ID_9307166,Human_RBP_ID_9398526,Human_RBP_ID_23050442,Human_RBP_ID_26351598,Human_RBP_ID_27512883 Human_Splice_Rec_709951,Human_Splice_Rec_709995,Human_Splice_Rec_710043,Human_Splice_Rec_710091,Human_Splice_Rec_710141,Human_Splice_Rec_710187,Human_Splice_Rec_710205,Human_Splice_Rec_710239,Human_Splice_Rec_710287,Human_Splice_Rec_710319,Human_Splice_Rec_710367,Human_Splice_Rec_710415,Human_Splice_Rec_710497,Human_Splice_Rec_710527 RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_119381,RMVar_hsa_circ_235452,RMVar_hsa_circ_235453,RMVar_hsa_circ_52376 82846 RMVar_ID_82846 Human_SNP_ID_256177583 m1A Human chr5 + 150374786 150374786 150374786 GGAGGACTCGCAGAGCAGCAGCGAGGAATCGGACAGTGAGGAGGAGGCGCCTGCTCAGGTGAGGC GGAGGACTCGCAGAGCAGCAGCGAGGAATCGGGCAGTGAGGAGGAGGCGCCTGCTCAGGTGAGGC A G TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:150374685..150374825;chr5:150374687..150374812 26863196 MeRIP-seq:(Medium) rs1179753647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73751,Human_RBP_ID_249809,Human_RBP_ID_945365,Human_RBP_ID_7405562,Human_RBP_ID_8886598,Human_RBP_ID_9307166,Human_RBP_ID_23050442,Human_RBP_ID_26351598,Human_RBP_ID_27512883 Human_Splice_Rec_709951,Human_Splice_Rec_709995,Human_Splice_Rec_710043,Human_Splice_Rec_710091,Human_Splice_Rec_710141,Human_Splice_Rec_710187,Human_Splice_Rec_710205,Human_Splice_Rec_710239,Human_Splice_Rec_710287,Human_Splice_Rec_710319,Human_Splice_Rec_710367,Human_Splice_Rec_710415,Human_Splice_Rec_710497,Human_Splice_Rec_710527 RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_119381,RMVar_hsa_circ_235452,RMVar_hsa_circ_235453,RMVar_hsa_circ_52376 82847 RMVar_ID_82847 Human_SNP_ID_256177741 m1A Human chr5 + 150375125 150375125 150375125 AGGACTCAAGAAGCAGCAGCGAGGAGTCAGACAGTGACAGAGAGGCACTGGCAGCCATGAATGCA AGGACTCAAGAAGCAGCAGCGAGGAGTCAGACGGTGACAGAGAGGCACTGGCAGCCATGAATGCA A G TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150374953..150375125 26863196 MeRIP-seq:(Medium) rs746215903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73753,Human_RBP_ID_7405564,Human_RBP_ID_8607477,Human_RBP_ID_8893784,Human_RBP_ID_15351099,Human_RBP_ID_18836316,Human_RBP_ID_22681812,Human_RBP_ID_24090863,Human_RBP_ID_26352767 Human_Splice_Rec_709953,Human_Splice_Rec_709997,Human_Splice_Rec_710045,Human_Splice_Rec_710093,Human_Splice_Rec_710143,Human_Splice_Rec_710207,Human_Splice_Rec_710241,Human_Splice_Rec_710289,Human_Splice_Rec_710321,Human_Splice_Rec_710369,Human_Splice_Rec_710417,Human_Splice_Rec_710499,Human_Splice_Rec_710529 RMVar_hsa_circ_17500,RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_119381,RMVar_hsa_circ_235452,RMVar_hsa_circ_235453,RMVar_hsa_circ_4136 82848 RMVar_ID_82848 Human_SNP_ID_256177875 m1A Human chr5 + 150375447 150375447 150375447 GCCCAGTGCCACCCGGGAAGGTGGGGCCTGCAACCCCCTCAGCCCAGGTGGGGAAGTGGGAGGAG GCCCAGTGCCACCCGGGAAGGTGGGGCCTGCAGCCCCCTCAGCCCAGGTGGGGAAGTGGGAGGAG A G TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150375397..150375546 26863196 MeRIP-seq:(Medium) rs760728462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3762767,Human_RBP_ID_3967557,Human_RBP_ID_5397566,Human_RBP_ID_8893786,Human_RBP_ID_18042238,Human_RBP_ID_22459792 Human_miRNA_ID_2553149,Human_miRNA_ID_2553150 RMVar_hsa_circ_17500,RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_265855,RMVar_hsa_circ_235452,RMVar_hsa_circ_4136 82849 RMVar_ID_82849 Human_SNP_ID_256178964 m1A Human chr5 - 150379033 150379033 150379033 CTGTGGCTTCTGGCCCCACTTGCCTTGGATGGAGACCTCTGCTTGGCTTGAGCAGCTGCAGTGAC CTGTGGCTTCTGGCCCCACTTGCCTTGGATGGGGACCTCTGCTTGGCTTGAGCAGCTGCAGTGAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:150378645..150379050 32194978 MeRIP-seq:(Medium) rs759007014 Functional Loss SNV dbSNP153 33..33 33 - - - 82850 RMVar_ID_82850 Human_SNP_ID_256179071 m1A Human chr5 + 150379368 150379368 150379368 AGGGCCAGAGGAGGACTCAGGGAGCAGTGAGGAGGAGTCAGACAGTGAGGAGGAGGCGGAGACGC AGGGCCAGAGGAGGACTCAGGGAGCAGTGAGGTGGAGTCAGACAGTGAGGAGGAGGCGGAGACGC A T TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:150379226..150379754 32194978 MeRIP-seq:(Medium) rs1169974134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73762,Human_RBP_ID_249815,Human_RBP_ID_838632,Human_RBP_ID_1039896,Human_RBP_ID_3762770,Human_RBP_ID_3968361,Human_RBP_ID_7405580,Human_RBP_ID_8607482,Human_RBP_ID_8886619,Human_RBP_ID_9307176,Human_RBP_ID_17662610,Human_RBP_ID_18413621,Human_RBP_ID_19016069,Human_RBP_ID_26352774,Human_RBP_ID_27826030 Human_Splice_Rec_709963,Human_Splice_Rec_710007,Human_Splice_Rec_710055,Human_Splice_Rec_710103,Human_Splice_Rec_710153,Human_Splice_Rec_710217,Human_Splice_Rec_710251,Human_Splice_Rec_710299,Human_Splice_Rec_710331,Human_Splice_Rec_710379,Human_Splice_Rec_710427,Human_Splice_Rec_710491,Human_Splice_Rec_710509,Human_Splice_Rec_710539,Human_Splice_Rec_710551,Human_Splice_Rec_710553 Human_miRNA_ID_2453608,Human_miRNA_ID_2453609 RMVar_hsa_circ_17500,RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_235452,RMVar_hsa_circ_348548 82851 RMVar_ID_82851 Human_SNP_ID_256179222 m1A Human chr5 + 150379669 150379668 150379670 TCGGCTGCCCAGGCAGGGAAGCAGGATGACTCAGGGAGCAGCAGCGAGGAATCAGACAGTGATGG TCGGCTGCCCAGGCAGGGAAGCAGGATGACTC__GGAGCAGCAGCGAGGAATCAGACAGTGATGG CAG C TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150379514..150379671 26863196 MeRIP-seq:(Medium) rs1554138819 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_249816,Human_RBP_ID_3968362,Human_RBP_ID_7405582,Human_RBP_ID_8886620,Human_RBP_ID_9307178,Human_RBP_ID_9398539,Human_RBP_ID_24386678,Human_RBP_ID_26351617 Human_Splice_Rec_709965,Human_Splice_Rec_710009,Human_Splice_Rec_710057,Human_Splice_Rec_710105,Human_Splice_Rec_710155,Human_Splice_Rec_710219,Human_Splice_Rec_710253,Human_Splice_Rec_710301,Human_Splice_Rec_710333,Human_Splice_Rec_710381,Human_Splice_Rec_710429,Human_Splice_Rec_710511,Human_Splice_Rec_710541,Human_Splice_Rec_710555 Clinvar_Rec_427 RMVar_hsa_circ_77779,RMVar_hsa_circ_87163,RMVar_hsa_circ_235451,RMVar_hsa_circ_235452,RMVar_hsa_circ_348548 82852 RMVar_ID_82852 Human_SNP_ID_256181459 m1A Human chr5 + 150388047 150388047 150388047 GAGCACAGCCAGGAGCTCCTCCTCCGAGAGCGAGGATGAGGACGTGATCCCCGCTACACAGTGCT GAGCACAGCCAGGAGCTCCTCCTCCGAGAGCGGGGATGAGGACGTGATCCCCGCTACACAGTGCT A G TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150387913..150388124 26863196 MeRIP-seq:(Medium) rs933272204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8893795,Human_RBP_ID_9307181 Human_Splice_Rec_709967,Human_Splice_Rec_710011,Human_Splice_Rec_710059,Human_Splice_Rec_710107,Human_Splice_Rec_710157,Human_Splice_Rec_710255,Human_Splice_Rec_710335,Human_Splice_Rec_710383,Human_Splice_Rec_710433,Human_Splice_Rec_710515,Human_Splice_Rec_710543,Human_Splice_Rec_710557 82853 RMVar_ID_82853 Human_SNP_ID_256181975 m1A Human chr5 + 150390011 150390011 150390011 AGTCGGATATCAGATGGCAAGAAACAGGAGGGACCAGCCACTCAGGTACCTGGTGGGCAAGGGAG AGTCGGATATCAGATGGCAAGAAACAGGAGGGCCCAGCCACTCAGGTACCTGGTGGGCAAGGGAG A C TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150389961..150391582 32194978 MeRIP-seq:(Medium) rs199924881 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9307182,Human_RBP_ID_15351306,Human_RBP_ID_22364778,Human_RBP_ID_26351620,Human_RBP_ID_27826032 Human_Splice_Rec_709969,Human_Splice_Rec_710013,Human_Splice_Rec_710061,Human_Splice_Rec_710109,Human_Splice_Rec_710159,Human_Splice_Rec_710257,Human_Splice_Rec_710337,Human_Splice_Rec_710385,Human_Splice_Rec_710435,Human_Splice_Rec_710517,Human_Splice_Rec_710545,Human_Splice_Rec_710559,Human_Splice_Rec_710561 RMVar_hsa_circ_83662,RMVar_hsa_circ_235454 82854 RMVar_ID_82854 Human_SNP_ID_256182914 m1A Human chr5 + 150393421 150393410 150393422 TATGACCCCTGGACTAACCCCAGCCAATTCCCAGGCCTCAAAAGCCACTCCCAAGCTAGACTCCA TATGACCCCTGGACTAACCCCA____________GCCTCAAAAGCCACTCCCAAGCTAGACTCCA AGCCAATTCCCAG A TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:150393351..150393578 32194978 MeRIP-seq:(Medium) rs1195467444 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_77468,Human_RBP_ID_943523,Human_RBP_ID_5477115,Human_RBP_ID_9306789,Human_RBP_ID_9398544,Human_RBP_ID_17298794,Human_RBP_ID_17412333,Human_RBP_ID_17528289,Human_RBP_ID_18836336 Human_Splice_Rec_709974,Human_Splice_Rec_710020,Human_Splice_Rec_710068,Human_Splice_Rec_710116,Human_Splice_Rec_710166,Human_Splice_Rec_710262,Human_Splice_Rec_710342,Human_Splice_Rec_710392,Human_Splice_Rec_710440,Human_Splice_Rec_710524 82855 RMVar_ID_82855 Human_SNP_ID_256183833 m1A Human chr5 + 150396653 150396653 150396653 AGGCCTCTGTTTCCCCAGAAAAGACCTCCACGACTTCCAAGGGGAAAGCAAAGAGAGACAAAGCA AGGCCTCTGTTTCCCCAGAAAAGACCTCCACGTCTTCCAAGGGGAAAGCAAAGAGAGACAAAGCA A T TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:150396289..150400108 32194978 MeRIP-seq:(Medium) rs1008294059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77471,Human_RBP_ID_943088,Human_RBP_ID_2909571,Human_RBP_ID_8943858,Human_RBP_ID_9398547,Human_RBP_ID_18413736,Human_RBP_ID_18471951,Human_RBP_ID_18836346,Human_RBP_ID_26351625,Human_RBP_ID_27827010 82856 RMVar_ID_82856 Human_SNP_ID_256183886 m1A Human chr5 - 150396796 150396795 150396796 TTCTTCTCCTTCTTGCTCTTTGGGTTGCTTTGATCTCCACCTTCAACCGTCCCCATCCCCTTCTG TTCTTCTCCTTCTTGCTCTTTGGGTTGCTTTGTCCTCCACCTTCAACCGTCCCCATCCCCTTCTG AT GA - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150396426..150396890 26863196 MeRIP-seq:(Medium) rs151344580 Functional Loss MNV dbSNP153 33..34 33 - - - Clinvar_Rec_428 82857 RMVar_ID_82857 Human_SNP_ID_256183888 m1A Human chr5 - 150396796 150396796 150396796 TTCTTCTCCTTCTTGCTCTTTGGGTTGCTTTGATCTCCACCTTCAACCGTCCCCATCCCCTTCTG TTCTTCTCCTTCTTGCTCTTTGGGTTGCTTTGTTCTCCACCTTCAACCGTCCCCATCCCCTTCTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150396426..150396890 26863196 MeRIP-seq:(Medium) rs956841291 Functional Loss SNV dbSNP153 33..33 33 - - - 82858 RMVar_ID_82858 Human_SNP_ID_256184578 m1A Human chr5 - 150399005 150399005 150399005 GCTCTGCTGTCTTCTTCTGTGAGGAGGGAAGTACGAGAGGCTCTCAGACCTGCAGCTTTTCCCCA GCTCTGCTGTCTTCTTCTGTGAGGAGGGAAGTTCGAGAGGCTCTCAGACCTGCAGCTTTTCCCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150399001..150399075 26863196 MeRIP-seq:(Medium) rs1316214933 Functional Loss SNV dbSNP153 33..33 33 - - - 82859 RMVar_ID_82859 Human_SNP_ID_256184781 m1A Human chr5 - 150399786 150399786 150399786 AGGAAATCCCTAGGGGAAGGAAACACATGCAGATGTCAAATTTCCTGACCCTTTTCCCCTGCAAG AGGAAATCCCTAGGGGAAGGAAACACATGCAGTTGTCAAATTTCCTGACCCTTTTCCCCTGCAAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150399783..150400166 26863196 MeRIP-seq:(Medium) rs1049246631 Functional Loss SNV dbSNP153 33..33 33 - - - 82860 RMVar_ID_82860 Human_SNP_ID_256184810 m1A Human chr5 + 150399916 150399916 150399916 TAAACTGTTACCTTCCCTCGCTCCACAGAAGAAGACAGCCAGCTTCAGGGGTCCCTGTGCTGGCC TAAACTGTTACCTTCCCTCGCTCCACAGAAGACGACAGCCAGCTTCAGGGGTCCCTGTGCTGGCC A C TCOF1 Ensembl:ENSG00000070814 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150399784..150400175 26863196 MeRIP-seq:(Medium) rs918988534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1990476,Human_RBP_ID_3762774,Human_RBP_ID_5121431,Human_RBP_ID_9398552,Human_RBP_ID_18195131,Human_RBP_ID_18413626,Human_RBP_ID_18836352,Human_RBP_ID_18956201,Human_RBP_ID_26350556,Human_RBP_ID_27827014 82861 RMVar_ID_82861 Human_SNP_ID_256184851 m1A Human chr5 - 150400077 150400074 150400077 CTTTGGGCATGTGGGGTCTGTGGAAGGAGAGGAGGTCACTTAAAAAAATACATATACTGTACACA CTTTGGGCATGTGGGGTCTGTGGAAGGAGAGG___TCACTTAAAAAAATACATATACTGTACACA ACCT A CD74 Ensembl:ENSG00000019582 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr5:150399826..150400192;chr5:150399976..150400125 26863196,26863410 MeRIP-seq:(Medium) rs1461906012 Functional Loss DEL dbSNP153 33..35 33 - - - 82862 RMVar_ID_82862 Human_SNP_ID_256192184 m1A Human chr5 - 150429051 150429051 150429051 CCACCAGAGACAGACCAACCCCACCAGAGACCAACCACACCAGAGACCAGCCCCACCAGAGACCA CCACCAGAGACAGACCAACCCCACCAGAGACCGACCACACCAGAGACCAGCCCCACCAGAGACCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150428896..150429373 26863196 MeRIP-seq:(Medium) rs576492508 Functional Loss SNV dbSNP153 33..33 33 - - - 82863 RMVar_ID_82863 Human_SNP_ID_256196596 m1A Human chr5 - 150444504 150444504 150444504 TCAGGAAATTCGAGGAACTGGCAGATGGGGCCACTTCATGTTCACATCCATCTGTTAGGTACTGG TCAGGAAATTCGAGGAACTGGCAGATGGGGCCGCTTCATGTTCACATCCATCTGTTAGGTACTGG T C RPS14 Ensembl:ENSG00000164587 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2073472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8607557,Human_RBP_ID_15351867 Human_Splice_Rec_710707 RMVar_hsa_circ_126237,RMVar_hsa_circ_89631,RMVar_hsa_circ_105764,RMVar_hsa_circ_83093,RMVar_hsa_circ_235464,RMVar_hsa_circ_235466,RMVar_hsa_circ_235465,RMVar_hsa_circ_235463 82864 RMVar_ID_82864 Human_SNP_ID_256197198 m1A Human chr5 + 150446762 150446762 150446762 CAAATCCAGGTGCTCCAGCACCCAAGCCCAGCAGGTTTTCTACCACCCAGCCATCCCCTCTGCGA CAAATCCAGGTGCTCCAGCACCCAAGCCCAGCCGGTTTTCTACCACCCAGCCATCCCCTCTGCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150446758..150447015 26863196 MeRIP-seq:(Medium) rs913061192 Functional Loss SNV dbSNP153 33..33 33 - - - 82865 RMVar_ID_82865 Human_SNP_ID_256197452 m1A Human chr5 - 150447705 150447705 150447705 AGAAATGGCACCTCGAAAGGGGAAGGAAAAGAAGGAAGAACAGGTCATCAGCCTCGGACCTCAGG AGAAATGGCACCTCGAAAGGGGAAGGAAAAGAGGGAAGAACAGGTCATCAGCCTCGGACCTCAGG T C RPS14 Ensembl:ENSG00000164587 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:150447605..150447775 26863410 MeRIP-seq:(Medium) rs1412974229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_635200,Human_RBP_ID_839220,Human_RBP_ID_945434,Human_RBP_ID_1648303,Human_RBP_ID_1990509,Human_RBP_ID_2909641,Human_RBP_ID_3762808,Human_RBP_ID_3968364,Human_RBP_ID_4817516,Human_RBP_ID_8267426,Human_RBP_ID_8607574,Human_RBP_ID_15352035,Human_RBP_ID_17662611,Human_RBP_ID_18195263,Human_RBP_ID_18448365,Human_RBP_ID_18836410,Human_RBP_ID_22460256,Human_RBP_ID_22827634,Human_RBP_ID_23051336,Human_RBP_ID_23214336,Human_RBP_ID_24504652,Human_RBP_ID_25938773,Human_RBP_ID_26351634 Human_Splice_Rec_710678,Human_Splice_Rec_710686,Human_Splice_Rec_710694,Human_Splice_Rec_710710,Human_Splice_Rec_710722 Human_miRNA_ID_1978710,Human_miRNA_ID_2713303 RMVar_hsa_circ_89631,RMVar_hsa_circ_105764,RMVar_hsa_circ_235464,RMVar_hsa_circ_235463,RMVar_hsa_circ_337480,RMVar_hsa_circ_235469,RMVar_hsa_circ_115038 82866 RMVar_ID_82866 Human_SNP_ID_256197453 m1A Human chr5 - 150447706 150447706 150447706 CAGAAATGGCACCTCGAAAGGGGAAGGAAAAGAAGGAAGAACAGGTCATCAGCCTCGGACCTCAG CAGAAATGGCACCTCGAAAGGGGAAGGAAAAGGAGGAAGAACAGGTCATCAGCCTCGGACCTCAG T C RPS14 Ensembl:ENSG00000164587 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:150447651..150447774;chr5:150447652..150447790 26863196 MeRIP-seq:(Medium) rs14926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_635200,Human_RBP_ID_839220,Human_RBP_ID_945434,Human_RBP_ID_1648303,Human_RBP_ID_1990509,Human_RBP_ID_2909641,Human_RBP_ID_3762808,Human_RBP_ID_3968364,Human_RBP_ID_4817516,Human_RBP_ID_5121719,Human_RBP_ID_8267426,Human_RBP_ID_8607574,Human_RBP_ID_15352035,Human_RBP_ID_17662611,Human_RBP_ID_18195263,Human_RBP_ID_18448365,Human_RBP_ID_18836410,Human_RBP_ID_21138343,Human_RBP_ID_22460256,Human_RBP_ID_22827634,Human_RBP_ID_23051336,Human_RBP_ID_23214336,Human_RBP_ID_24504652,Human_RBP_ID_25938773,Human_RBP_ID_26351634,Human_RBP_ID_26523408 Human_Splice_Rec_710678,Human_Splice_Rec_710686,Human_Splice_Rec_710694,Human_Splice_Rec_710710,Human_Splice_Rec_710722 Human_miRNA_ID_1978710 RMVar_hsa_circ_89631,RMVar_hsa_circ_105764,RMVar_hsa_circ_235464,RMVar_hsa_circ_235463,RMVar_hsa_circ_337480,RMVar_hsa_circ_235469,RMVar_hsa_circ_115038 82867 RMVar_ID_82867 Human_SNP_ID_256197934 m1A Human chr5 - 150449592 150449592 150449592 TCTTTCCGTGGGAACCGAGCTAGGTGCCGGGCAAGAGACGCGCGGCTGGCCCACCTGGATCCTGG TCTTTCCGTGGGAACCGAGCTAGGTGCCGGGCGAGAGACGCGCGGCTGGCCCACCTGGATCCTGG T C RPS14 Ensembl:ENSG00000164587 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr5:150449582..150449707;chr5:150449551..150449750 26863196,26863410 MeRIP-seq:(Medium) rs576784781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839225,Human_RBP_ID_4817518,Human_RBP_ID_5326608,Human_RBP_ID_5396825,Human_RBP_ID_9354604,Human_RBP_ID_15352088,Human_RBP_ID_18425200,Human_RBP_ID_19128216,Human_RBP_ID_24090954 RMVar_hsa_circ_105764,RMVar_hsa_circ_235463,RMVar_hsa_circ_235469,RMVar_hsa_circ_115038 82868 RMVar_ID_82868 Human_SNP_ID_256207976 m1A Human chr5 - 150486574 150486574 150486574 GCCCCGCGCGGCCCCCTACCCTTTGTCCTCCCACCCCCGCGCGCGGGGCCCGGCCGACTCCACCC GCCCCGCGCGGCCCCCTACCCTTTGTCCTCCCCCCCCCGCGCGCGGGGCCCGGCCGACTCCACCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150486555..150486686 26863196 MeRIP-seq:(Medium) rs919129381 Functional Loss SNV dbSNP153 33..33 33 - - - 82869 RMVar_ID_82869 Human_SNP_ID_256220721 m1A Human chr5 + 150538110 150538110 150538110 GGAATAAGCCACGCTGCCACATGAGGAAGAGCACTCAAGGCAGAGAACACAAGTGCAAAGGCCCT GGAATAAGCCACGCTGCCACATGAGGAAGAGCGCTCAAGGCAGAGAACACAAGTGCAAAGGCCCT A G NDST1 Ensembl:ENSG00000070614 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150538107..150538308 26863196 MeRIP-seq:(Medium) rs980887609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102938,RMVar_hsa_circ_64297,RMVar_hsa_circ_78043,RMVar_hsa_circ_95798,RMVar_hsa_circ_13658,RMVar_hsa_circ_18018,RMVar_hsa_circ_323967,RMVar_hsa_circ_235472,RMVar_hsa_circ_112546,RMVar_hsa_circ_235475,RMVar_hsa_circ_121189,RMVar_hsa_circ_89710,RMVar_hsa_circ_235476,RMVar_hsa_circ_235478,RMVar_hsa_circ_235479,RMVar_hsa_circ_235477 82870 RMVar_ID_82870 Human_SNP_ID_256221652 m1A Human chr5 + 150541636 150541636 150541636 GGTCCAAGGAGAAGACGTGTGACCGCTTCCCAAAGCTCCTCATCATCGGCCCCCAGAAAACAGGC GGTCCAAGGAGAAGACGTGTGACCGCTTCCCAGAGCTCCTCATCATCGGCCCCCAGAAAACAGGC A G NDST1 Ensembl:ENSG00000070614 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:150541535..150541707 26863196 MeRIP-seq:(Medium) rs1474771550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946086 Human_Splice_Rec_710756,Human_Splice_Rec_710788 RMVar_hsa_circ_102938,RMVar_hsa_circ_64297,RMVar_hsa_circ_78043,RMVar_hsa_circ_13658,RMVar_hsa_circ_235472,RMVar_hsa_circ_121189,RMVar_hsa_circ_89710,RMVar_hsa_circ_71251,RMVar_hsa_circ_235476,RMVar_hsa_circ_235478,RMVar_hsa_circ_235477,RMVar_hsa_circ_79937,RMVar_hsa_circ_235481,RMVar_hsa_circ_51111,RMVar_hsa_circ_235482,RMVar_hsa_circ_235484,RMVar_hsa_circ_290447,RMVar_hsa_circ_326434,RMVar_hsa_circ_364073,RMVar_hsa_circ_290535,RMVar_hsa_circ_38836,RMVar_hsa_circ_235483 82871 RMVar_ID_82871 Human_SNP_ID_256225014 m1A Human chr5 + 150555066 150555066 150555066 AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCATGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCGTGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA A G NDST1 Ensembl:ENSG00000070614 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150555015..150555140 26863196 MeRIP-seq:(Medium) rs143181608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4851580,Human_RBP_ID_26529409 Human_miRNA_ID_266587,Human_miRNA_ID_2082783,Human_miRNA_ID_2380364,Human_miRNA_ID_3023377 RMVar_hsa_circ_89710,RMVar_hsa_circ_235476 82872 RMVar_ID_82872 Human_SNP_ID_256225015 m1A Human chr5 + 150555066 150555066 150555066 AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCATGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCTTGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA A T NDST1 Ensembl:ENSG00000070614 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150555015..150555140 26863196 MeRIP-seq:(Medium) rs143181608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4851580,Human_RBP_ID_26529409 Human_miRNA_ID_266587,Human_miRNA_ID_2082783,Human_miRNA_ID_2380364,Human_miRNA_ID_3023377 RMVar_hsa_circ_89710,RMVar_hsa_circ_235476 82873 RMVar_ID_82873 Human_SNP_ID_256242876 m1A Human chr5 + 150624852 150624852 150624852 CCTCGGGGCGGGGCGCGCTGACGGACGCGGCCAGGTGTGCCGAGGCGGCGGCGCCCGGGAGCTCG CCTCGGGGCGGGGCGCGCTGACGGACGCGGCCTGGTGTGCCGAGGCGGCGGCGCCCGGGAGCTCG A T SYNPO Ensembl:ENSG00000171992 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150624706..150625242 26863196 MeRIP-seq:(Medium) rs886977988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5214549 Human_Splice_Rec_710809 82874 RMVar_ID_82874 Human_SNP_ID_256244383 m1A Human chr5 + 150631315 150631315 150631315 TTTAGGGAAGAGGCAGAGAGTGTTGTGGCAGGAGAATGTGACCTCTGAGGGCCTTGGGACCTGTG TTTAGGGAAGAGGCAGAGAGTGTTGTGGCAGGGGAATGTGACCTCTGAGGGCCTTGGGACCTGTG A G SYNPO Ensembl:ENSG00000171992 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150631297..150631592 26863196 MeRIP-seq:(Medium) rs989693405 Functional Loss SNV dbSNP153 33..33 33 - - - 82875 RMVar_ID_82875 Human_SNP_ID_256248646 m1A Human chr5 + 150649066 150649066 150649066 GATGGAGAGGAGCCCCATGCTAGAGAGACGACATTTTGGGGAGAAGGCCCCGGCTCCCCAGCCCC GATGGAGAGGAGCCCCATGCTAGAGAGACGACGTTTTGGGGAGAAGGCCCCGGCTCCCCAGCCCC A G SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150649015..150649188 26863196 MeRIP-seq:(Medium) rs779190452 Functional Loss SNV dbSNP153 33..33 33 - - - 82876 RMVar_ID_82876 Human_SNP_ID_256248651 m1A Human chr5 + 150649077 150649077 150649077 GCCCCATGCTAGAGAGACGACATTTTGGGGAGAAGGCCCCGGCTCCCCAGCCCCCCAGTTTGCCA GCCCCATGCTAGAGAGACGACATTTTGGGGAGGAGGCCCCGGCTCCCCAGCCCCCCAGTTTGCCA A G SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150649029..150649189 26863196 MeRIP-seq:(Medium) rs41520647 Functional Loss SNV dbSNP153 33..33 33 - - - 82877 RMVar_ID_82877 Human_SNP_ID_256248796 m1A Human chr5 - 150649466 150649466 150649466 TGCCGCCGCTTCTCATCCGCTGTCTGTACCAGATCCAGCAAGTCTGGATTCGGGGTCACCTTGGG TGCCGCCGCTTCTCATCCGCTGTCTGTACCAGGTCCAGCAAGTCTGGATTCGGGGTCACCTTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150649416..150649627 26863196 MeRIP-seq:(Medium) rs1241892358 Functional Loss SNV dbSNP153 33..33 33 - - - 82878 RMVar_ID_82878 Human_SNP_ID_256248929 m1A Human chr5 + 150649761 150649761 150649761 CCCGCCGCCAGTCACGGATGGAGAAATATGTCATCGAGTCTTCAAGCCACACGCCAGAGCTGGCC CCCGCCGCCAGTCACGGATGGAGAAATATGTCTTCGAGTCTTCAAGCCACACGCCAGAGCTGGCC A T SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150649710..150650263 26863196 MeRIP-seq:(Medium) rs759496960 Functional Loss SNV dbSNP153 33..33 33 - - - 82879 RMVar_ID_82879 Human_SNP_ID_256249055 m1A Human chr5 + 150650076 150650076 150650076 CCGCCAAGCCCAGCTCCTTGGACCTGGTGCCCAACCTGCCCAAGGGGGCTCTCCCTCCATCTCCT CCGCCAAGCCCAGCTCCTTGGACCTGGTGCCCCACCTGCCCAAGGGGGCTCTCCCTCCATCTCCT A C SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:150649852..150650238;chr5:150650026..150650225 26863196 MeRIP-seq:(Medium) rs1429864228 Functional Loss SNV dbSNP153 33..33 33 - - - 82880 RMVar_ID_82880 Human_SNP_ID_256249537 m1A Human chr5 - 150651559 150651559 150651559 CCCAGGCATCCCTTGGCCTCCTGCAGCAGCTCATTCCAACCCTTCCCTCACCAGGTCACCCTCAC CCCAGGCATCCCTTGGCCTCCTGCAGCAGCTCGTTCCAACCCTTCCCTCACCAGGTCACCCTCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150651508..150651672 26863196 MeRIP-seq:(Medium) rs1346934422 Functional Loss SNV dbSNP153 33..33 33 - - - 82881 RMVar_ID_82881 Human_SNP_ID_256250935 m1A Human chr5 - 150656858 150656858 150656858 GGGGACTGGTGCAGGACGAAGGACCGGCGGGCAACGGGCTCCGCGGGATGGGCGCGAAGGCTGCC GGGGACTGGTGCAGGACGAAGGACCGGCGGGCGACGGGCTCCGCGGGATGGGCGCGAAGGCTGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150656815..150656952 26863196 MeRIP-seq:(Medium) rs1311491137 Functional Loss SNV dbSNP153 33..33 33 - - - 82882 RMVar_ID_82882 Human_SNP_ID_256250969 m1A Human chr5 + 150656914 150656914 150656914 CCAGTCCCCGGAGCCCGCTGCCCGCGCCTCCCAGGCCCTTCCTCTACCGCCGCTCGCCCACGGAC CCAGTCCCCGGAGCCCGCTGCCCGCGCCTCCCTGGCCCTTCCTCTACCGCCGCTCGCCCACGGAC A T SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150656480..150657029 26863196 MeRIP-seq:(Medium) rs1433620248 Functional Loss SNV dbSNP153 33..33 33 - - - 82883 RMVar_ID_82883 Human_SNP_ID_256251539 m1A Human chr5 + 150658729 150658729 150658729 CTTACCGGGGTGATGTTAGATCTGGAACCCCCAAGTGAGGCTGGAGGGAGTTAAGGTCAGTATGG CTTACCGGGGTGATGTTAGATCTGGAACCCCCGAGTGAGGCTGGAGGGAGTTAAGGTCAGTATGG A G SYNPO Ensembl:ENSG00000171992 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150658543..150658900 26863196 MeRIP-seq:(Medium) rs1408616793 Functional Loss SNV dbSNP153 33..33 33 - - - 82884 RMVar_ID_82884 Human_SNP_ID_256259798 m1A Human chr5 - 150691388 150691386 150691389 ATATTTTTTGGTCGGGGGAAAAATTGACCTGCAGTAAAAAAACCTTTGACCATTTTTATGTCCAT ATATTTTTTGGTCGGGGGAAAAATTGACCTG___TAAAAAAACCTTTGACCATTTTTATGTCCAT ACTG A RBM22 Ensembl:ENSG00000086589 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150691338..150691586 32194978 MeRIP-seq:(Medium) rs147788860 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5121440,Human_RBP_ID_5151348,Human_RBP_ID_7405982,Human_RBP_ID_8607654,Human_RBP_ID_8886667,Human_RBP_ID_18042366,Human_RBP_ID_18836457,Human_RBP_ID_21900796,Human_RBP_ID_22297362,Human_RBP_ID_23051338,Human_RBP_ID_24091093,Human_RBP_ID_27076533 Human_miRNA_ID_621691 RMVar_hsa_circ_76972,RMVar_hsa_circ_119687,RMVar_hsa_circ_121203,RMVar_hsa_circ_82288,RMVar_hsa_circ_99194,RMVar_hsa_circ_78020,RMVar_hsa_circ_235488,RMVar_hsa_circ_235490,RMVar_hsa_circ_235492,RMVar_hsa_circ_235493,RMVar_hsa_circ_235491,RMVar_hsa_circ_235489 82885 RMVar_ID_82885 Human_SNP_ID_256259799 m1A Human chr5 - 150691388 150691388 150691388 ATATTTTTTGGTCGGGGGAAAAATTGACCTGCAGTAAAAAAACCTTTGACCATTTTTATGTCCAT ATATTTTTTGGTCGGGGGAAAAATTGACCTGCCGTAAAAAAACCTTTGACCATTTTTATGTCCAT T G RBM22 Ensembl:ENSG00000086589 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150691338..150691586 32194978 MeRIP-seq:(Medium) rs909482513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5121440,Human_RBP_ID_5151348,Human_RBP_ID_7405982,Human_RBP_ID_8607654,Human_RBP_ID_8886667,Human_RBP_ID_18042366,Human_RBP_ID_18836457,Human_RBP_ID_21900796,Human_RBP_ID_22297362,Human_RBP_ID_23051338,Human_RBP_ID_24091093,Human_RBP_ID_27076533 Human_miRNA_ID_621691 RMVar_hsa_circ_76972,RMVar_hsa_circ_119687,RMVar_hsa_circ_121203,RMVar_hsa_circ_82288,RMVar_hsa_circ_99194,RMVar_hsa_circ_78020,RMVar_hsa_circ_235488,RMVar_hsa_circ_235490,RMVar_hsa_circ_235492,RMVar_hsa_circ_235493,RMVar_hsa_circ_235491,RMVar_hsa_circ_235489 82886 RMVar_ID_82886 Human_SNP_ID_256259917 m1A Human chr5 + 150691863 150691863 150691863 GCATGAAAGGAGGGGGTGGTCCCATTGGGTGGAACATGTGTGGCCCAAAACCTGCAGATACGAGA GCATGAAAGGAGGGGGTGGTCCCATTGGGTGGCACATGTGTGGCCCAAAACCTGCAGATACGAGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150691684..150692896 32194978 MeRIP-seq:(Medium) rs202091279 Functional Loss SNV dbSNP153 33..33 33 - - - 82887 RMVar_ID_82887 Human_SNP_ID_256259918 m1A Human chr5 + 150691863 150691863 150691863 GCATGAAAGGAGGGGGTGGTCCCATTGGGTGGAACATGTGTGGCCCAAAACCTGCAGATACGAGA GCATGAAAGGAGGGGGTGGTCCCATTGGGTGGGACATGTGTGGCCCAAAACCTGCAGATACGAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150691684..150692896 32194978 MeRIP-seq:(Medium) rs202091279 Functional Loss SNV dbSNP153 33..33 33 - - - 82888 RMVar_ID_82888 Human_SNP_ID_256262102 m1A Human chr5 + 150701020 150701020 150701020 TGAGAGCGTCCGGAGGTAGCTGTAGCTTCCGAATTGGGAGAGAGGACCGCCACAATCCCGTCAAG TGAGAGCGTCCGGAGGTAGCTGTAGCTTCCGACTTGGGAGAGAGGACCGCCACAATCCCGTCAAG A C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150700969..150701036 26863196 MeRIP-seq:(Medium) rs1388417039 Functional Loss SNV dbSNP153 33..33 33 - - - 82889 RMVar_ID_82889 Human_SNP_ID_256264116 m1A Human chr5 + 150709036 150709036 150709036 GGGATCTAACTTTCCTGTGGTGGTGCATACTGACTAGCATTAAAATTTTTGCACCTCATCTAATA GGGATCTAACTTTCCTGTGGTGGTGCATACTGGCTAGCATTAAAATTTTTGCACCTCATCTAATA A G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150708986..150709087 32194978 MeRIP-seq:(Medium) rs1168046871 Functional Loss SNV dbSNP153 33..33 33 - - - 82890 RMVar_ID_82890 Human_SNP_ID_256272216 m1A Human chr5 + 150742135 150742135 150742135 CCTTTACTTACCCGTTGTGTGTGAGGATTTTCAGGTTCCTGCCAACCGCCACTAGCTACAAAATA CCTTTACTTACCCGTTGTGTGTGAGGATTTTCTGGTTCCTGCCAACCGCCACTAGCTACAAAATA A T RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150742115..150742875 32194978 MeRIP-seq:(Medium) rs1409077734 Functional Loss SNV dbSNP153 33..33 33 - - - 82891 RMVar_ID_82891 Human_SNP_ID_256276690 m1A Human chr5 + 150758895 150758895 150758895 TGAGACACACATTCCAGCGACCGCAGTTCGCTACAATAGCGGCAGAAGTAGAGTTGCGAGAGCGG TGAGACACACATTCCAGCGACCGCAGTTCGCTGCAATAGCGGCAGAAGTAGAGTTGCGAGAGCGG A G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150758873..150758954 26863196 MeRIP-seq:(Medium) rs1184539516 Functional Loss SNV dbSNP153 33..33 33 - - - 82892 RMVar_ID_82892 Human_SNP_ID_256308465 m1A Human chr5 - 150898058 150898058 150898058 AGATGAATATCAGGCAGATGGGAGACAAGGGAAGTGAAATATCAATTTATGTTTTTTTAATTGAT AGATGAATATCAGGCAGATGGGAGACAAGGGACGTGAAATATCAATTTATGTTTTTTTAATTGAT T G ZNF300 Ensembl:ENSG00000145908 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs776095721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19127514,Human_RBP_ID_23041591 Human_Splice_Rec_711185 82893 RMVar_ID_82893 Human_SNP_ID_256309752 m1A Human chr5 + 150903976 150903976 150903976 AGACAGATTATTTTATATGGGGGTATCAAAACATCTGGAAGGAAACAAAAGAAACAATCATACTC AGACAGATTATTTTATATGGGGGTATCAAAACTTCTGGAAGGAAACAAAAGAAACAATCATACTC A T RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:150903959..150904028 26863196 MeRIP-seq:(Medium) rs941595539 Functional Loss SNV dbSNP153 33..33 33 - - - 82894 RMVar_ID_82894 Human_SNP_ID_256337661 m1A Human chr5 + 151030695 151030695 151030695 ATCAGCTGGCTCTGCAAGATGAAGGTGGAGCCAAATGACACAATCTGGTCTCACTGAGGCCCCTC ATCAGCTGGCTCTGCAAGATGAAGGTGGAGCCGAATGACACAATCTGGTCTCACTGAGGCCCCTC A G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151030593..151030744 32194978 MeRIP-seq:(Medium) rs750898741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18042502 82895 RMVar_ID_82895 Human_SNP_ID_256337883 m1A Human chr5 - 151031689 151031687 151031689 TGGCTGGAGCCAAGAACAAGGTAGGGAAAGAGAGGGGCAACGCAGGGTTCAGGACGTAGCCGGGT TGGCTGGAGCCAAGAACAAGGTAGGGAAAGAG__GGGCAACGCAGGGTTCAGGACGTAGCCGGGT CCT C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:151031683..151031781 26863196 MeRIP-seq:(Medium) rs1334151992 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_235525 82896 RMVar_ID_82896 Human_SNP_ID_256338067 m1A Human chr5 - 151032338 151032338 151032338 GGCGTCTACCCTGTGGAGGGGTTCGAAATCCAAATCAGAGCTCCCAAGTGATGGACCCTCCCACA GGCGTCTACCCTGTGGAGGGGTTCGAAATCCAGATCAGAGCTCCCAAGTGATGGACCCTCCCACA T C TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:151032248..151032379;chr5:151032254..151032359 26863196 MeRIP-seq:(Medium) rs778159697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4818123,Human_RBP_ID_18042503,Human_RBP_ID_18836558 Human_Splice_Rec_711282,Human_Splice_Rec_711283,Human_Splice_Rec_711314,Human_Splice_Rec_711315,Human_Splice_Rec_711380,Human_Splice_Rec_711381,Human_Splice_Rec_711412,Human_Splice_Rec_711413,Human_Splice_Rec_711442,Human_Splice_Rec_711443,Human_Splice_Rec_711452,Human_Splice_Rec_711453,Human_Splice_Rec_711484,Human_Splice_Rec_711485,Human_Splice_Rec_711512,Human_Splice_Rec_711513,Human_Splice_Rec_711544,Human_Splice_Rec_711545,Human_Splice_Rec_711576,Human_Splice_Rec_711577,Human_Splice_Rec_711630,Human_Splice_Rec_711631 Human_miRNA_ID_2478616,Human_miRNA_ID_2478617 RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_369762,RMVar_hsa_circ_235525,RMVar_hsa_circ_235528 82897 RMVar_ID_82897 Human_SNP_ID_256338068 m1A Human chr5 - 151032338 151032338 151032338 GGCGTCTACCCTGTGGAGGGGTTCGAAATCCAAATCAGAGCTCCCAAGTGATGGACCCTCCCACA GGCGTCTACCCTGTGGAGGGGTTCGAAATCCACATCAGAGCTCCCAAGTGATGGACCCTCCCACA T G TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:151032248..151032379;chr5:151032254..151032359 26863196 MeRIP-seq:(Medium) rs778159697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4818123,Human_RBP_ID_18042503,Human_RBP_ID_18836558 Human_Splice_Rec_711282,Human_Splice_Rec_711283,Human_Splice_Rec_711314,Human_Splice_Rec_711315,Human_Splice_Rec_711380,Human_Splice_Rec_711381,Human_Splice_Rec_711412,Human_Splice_Rec_711413,Human_Splice_Rec_711442,Human_Splice_Rec_711443,Human_Splice_Rec_711452,Human_Splice_Rec_711453,Human_Splice_Rec_711484,Human_Splice_Rec_711485,Human_Splice_Rec_711512,Human_Splice_Rec_711513,Human_Splice_Rec_711544,Human_Splice_Rec_711545,Human_Splice_Rec_711576,Human_Splice_Rec_711577,Human_Splice_Rec_711630,Human_Splice_Rec_711631 Human_miRNA_ID_2478616,Human_miRNA_ID_2478617 RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_369762,RMVar_hsa_circ_235525,RMVar_hsa_circ_235528 82898 RMVar_ID_82898 Human_SNP_ID_256338427 m1A Human chr5 - 151033658 151033658 151033658 ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCATGGCCATGGAGCACCCGCCCCCACTCCCCAAC ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCGTGGCCATGGAGCACCCGCCCCCACTCCCCAAC T C TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs143590032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165355 Human_Splice_Rec_711281,Human_Splice_Rec_711313,Human_Splice_Rec_711379,Human_Splice_Rec_711411,Human_Splice_Rec_711451,Human_Splice_Rec_711483,Human_Splice_Rec_711543,Human_Splice_Rec_711575 Human_miRNA_ID_2387968,Human_miRNA_ID_2392701 RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_235525 82899 RMVar_ID_82899 Human_SNP_ID_256338428 m1A Human chr5 - 151033658 151033658 151033658 ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCATGGCCATGGAGCACCCGCCCCCACTCCCCAAC ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCCTGGCCATGGAGCACCCGCCCCCACTCCCCAAC T G TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs143590032 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_165355 Human_Splice_Rec_711281,Human_Splice_Rec_711313,Human_Splice_Rec_711379,Human_Splice_Rec_711411,Human_Splice_Rec_711451,Human_Splice_Rec_711483,Human_Splice_Rec_711543,Human_Splice_Rec_711575 Human_miRNA_ID_2387968,Human_miRNA_ID_2392701 RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_235525 82900 RMVar_ID_82900 Human_SNP_ID_256339103 m1A Human chr5 + 151035651 151035651 151035651 TCCACTTGCTTCTTCAGCTCTTCCTTCTCCTCATTCATGCGCTCACGATCACTGCGCTCCCTCTG TCCACTTGCTTCTTCAGCTCTTCCTTCTCCTCGTTCATGCGCTCACGATCACTGCGCTCCCTCTG A G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:151035549..151035736 26863196 MeRIP-seq:(Medium) rs770827067 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 82901 RMVar_ID_82901 Human_SNP_ID_256341579 m1A Human chr5 - 151045892 151045892 151045892 AGAGGTGGTGGCCTTGGGCGCAGCCGAGAAGAAGGTGAAGATGCTGGAGCAGCAGCGCAGTGAGG AGAGGTGGTGGCCTTGGGCGCAGCCGAGAAGACGGTGAAGATGCTGGAGCAGCAGCGCAGTGAGG T G TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151037426..151045975 32194978 MeRIP-seq:(Medium) rs766630886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250183,Human_RBP_ID_839122,Human_RBP_ID_944719,Human_RBP_ID_19016080,Human_RBP_ID_27827023 Human_Splice_Rec_711268,Human_Splice_Rec_711269,Human_Splice_Rec_711300,Human_Splice_Rec_711301,Human_Splice_Rec_711332,Human_Splice_Rec_711333,Human_Splice_Rec_711366,Human_Splice_Rec_711367,Human_Splice_Rec_711398,Human_Splice_Rec_711399,Human_Splice_Rec_711430,Human_Splice_Rec_711431,Human_Splice_Rec_711470,Human_Splice_Rec_711471,Human_Splice_Rec_711498,Human_Splice_Rec_711499,Human_Splice_Rec_711530,Human_Splice_Rec_711531,Human_Splice_Rec_711562,Human_Splice_Rec_711563,Human_Splice_Rec_711592,Human_Splice_Rec_711593,Human_Splice_Rec_711618,Human_Splice_Rec_711619,Human_Splice_Rec_711634,Human_Splice_Rec_711639,Human_Splice_Rec_711654 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_235530,RMVar_hsa_circ_361863,RMVar_hsa_circ_349118 82902 RMVar_ID_82902 Human_SNP_ID_256342970 m1A Human chr5 - 151052100 151052100 151052100 AGTGGGGGCTGCAGGAGGAGGGGCTGGTGTGCAGCACTGATTTCTGGGTTGAGGACCGTGGCTCT AGTGGGGGCTGCAGGAGGAGGGGCTGGTGTGCGGCACTGATTTCTGGGTTGAGGACCGTGGCTCT T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:151052097..151052200 26863196 MeRIP-seq:(Medium) rs531541995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5395797 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_58639,RMVar_hsa_circ_235530,RMVar_hsa_circ_361863,RMVar_hsa_circ_349118,RMVar_hsa_circ_335155,RMVar_hsa_circ_19862 82903 RMVar_ID_82903 Human_SNP_ID_256342975 m1A Human chr5 - 151052114 151052114 151052114 GAGAAGGGGTGAGGAGTGGGGGCTGCAGGAGGAGGGGCTGGTGTGCAGCACTGATTTCTGGGTTG GAGAAGGGGTGAGGAGTGGGGGCTGCAGGAGGTGGGGCTGGTGTGCAGCACTGATTTCTGGGTTG T A TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151052110..151052198 26863196 MeRIP-seq:(Medium) rs1413916912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5395797 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_58639,RMVar_hsa_circ_235530,RMVar_hsa_circ_361863,RMVar_hsa_circ_349118,RMVar_hsa_circ_335155,RMVar_hsa_circ_19862 82904 RMVar_ID_82904 Human_SNP_ID_256345763 m1A Human chr5 - 151062202 151062202 151062202 CTGTGCTTTCTTGATTCTCCAGGAAAGGACTCAAATGTCACAGCATCTCCCACAGCCCCTGCATG CTGTGCTTTCTTGATTCTCCAGGAAAGGACTCCAATGTCACAGCATCTCCCACAGCCCCTGCATG T G TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151062151..151062225 32194978 MeRIP-seq:(Medium) rs372038140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967563 Human_Splice_Rec_711258,Human_Splice_Rec_711259,Human_Splice_Rec_711290,Human_Splice_Rec_711291,Human_Splice_Rec_711322,Human_Splice_Rec_711323,Human_Splice_Rec_711356,Human_Splice_Rec_711357,Human_Splice_Rec_711388,Human_Splice_Rec_711389,Human_Splice_Rec_711420,Human_Splice_Rec_711421,Human_Splice_Rec_711460,Human_Splice_Rec_711461,Human_Splice_Rec_711488,Human_Splice_Rec_711489,Human_Splice_Rec_711520,Human_Splice_Rec_711521,Human_Splice_Rec_711552,Human_Splice_Rec_711553,Human_Splice_Rec_711582,Human_Splice_Rec_711583,Human_Splice_Rec_711608,Human_Splice_Rec_711609,Human_Splice_Rec_711644,Human_Splice_Rec_711645,Human_Splice_Rec_711662,Human_Splice_Rec_711663,Human_Splice_Rec_711670,Human_Splice_Rec_711671 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_67248,RMVar_hsa_circ_335155,RMVar_hsa_circ_24106,RMVar_hsa_circ_19862,RMVar_hsa_circ_235531,RMVar_hsa_circ_280679,RMVar_hsa_circ_328695,RMVar_hsa_circ_329693 82905 RMVar_ID_82905 Human_SNP_ID_256346494 m1A Human chr5 + 151065049 151065049 151065049 GCTCAAAAGCTGCGGATGCCTCTCCTGAGGGCACGCTGCCCCCAGGGTCGTAGATCCGGTACGGT GCTCAAAAGCTGCGGATGCCTCTCCTGAGGGCCCGCTGCCCCCAGGGTCGTAGATCCGGTACGGT A C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151063601..151078428 32194978 MeRIP-seq:(Medium) rs1440859504 Functional Loss SNV dbSNP153 33..33 33 - - - 82906 RMVar_ID_82906 Human_SNP_ID_256365261 m1A Human chr5 - 151140233 151140233 151140233 CCCTCTACTTTTTTCTCCACAGGGTGCCAAGTACCGGGGCTCCATCCATGACTTCCCAGGCTTTG CCCTCTACTTTTTTCTCCACAGGGTGCCAAGTCCCGGGGCTCCATCCATGACTTCCCAGGCTTTG T G ANXA6 Ensembl:ENSG00000197043 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151140109..151140297 26863196 MeRIP-seq:(Medium) rs540355415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4818270 Human_Splice_Rec_711680,Human_Splice_Rec_711681,Human_Splice_Rec_711733,Human_Splice_Rec_711782,Human_Splice_Rec_711783,Human_Splice_Rec_711808,Human_Splice_Rec_711809,Human_Splice_Rec_711844,Human_Splice_Rec_711845,Human_Splice_Rec_711856,Human_Splice_Rec_711857,Human_Splice_Rec_711890,Human_Splice_Rec_711891,Human_Splice_Rec_711904,Human_Splice_Rec_711905,Human_Splice_Rec_711916,Human_Splice_Rec_711917,Human_Splice_Rec_711928,Human_Splice_Rec_711929,Human_Splice_Rec_711936,Human_Splice_Rec_711937 RMVar_hsa_circ_117623,RMVar_hsa_circ_235542,RMVar_hsa_circ_122695,RMVar_hsa_circ_106766,RMVar_hsa_circ_235566,RMVar_hsa_circ_235567,RMVar_hsa_circ_46155 82907 RMVar_ID_82907 Human_SNP_ID_256385381 m1A Human chr5 - 151223959 151223959 151223959 TCCGGGAGCCCCCGGAGGAGGATGGGCTGCAGACACAGCAGGCTGAGCAGCTGCAAACCCCCGAA TCCGGGAGCCCCCGGAGGAGGATGGGCTGCAGTCACAGCAGGCTGAGCAGCTGCAAACCCCCGAA T A CCDC69 Ensembl:ENSG00000198624 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:151223957..151224044 26863196 MeRIP-seq:(Medium) rs942658210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_711951,Human_Splice_Rec_711967,Human_Splice_Rec_712009 82908 RMVar_ID_82908 Human_SNP_ID_256385411 m1A Human chr5 - 151224027 151224027 151224027 GGGCGCGGAGCGGGCAGCGGGGCCCGGATCGCAGGCTCCTCTGGGGGCCCCGGAGTTGGGAAGCG GGGCGCGGAGCGGGCAGCGGGGCCCGGATCGCCGGCTCCTCTGGGGGCCCCGGAGTTGGGAAGCG T G CCDC69 Ensembl:ENSG00000198624 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:151223926..151224075 26863410 MeRIP-seq:(Medium) rs1461734081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845448 82909 RMVar_ID_82909 Human_SNP_ID_256392577 m1A Human chr5 + 151253217 151253217 151253217 GCAGTTAACTCCGCCCTGACCCACCCTTCCCGATGCAGTCCCTGATGCAGGCTCCCCTCCTGATC GCAGTTAACTCCGCCCTGACCCACCCTTCCCGCTGCAGTCCCTGATGCAGGCTCCCCTCCTGATC A C GM2A Ensembl:ENSG00000196743 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151253144..151259809 26863196 MeRIP-seq:(Medium) rs1400709234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788993,Human_RBP_ID_4846105,Human_RBP_ID_17415402,Human_RBP_ID_18956763,Human_RBP_ID_27513042 Human_Splice_Rec_712017 82910 RMVar_ID_82910 Human_SNP_ID_256392578 m1A Human chr5 + 151253217 151253217 151253217 GCAGTTAACTCCGCCCTGACCCACCCTTCCCGATGCAGTCCCTGATGCAGGCTCCCCTCCTGATC GCAGTTAACTCCGCCCTGACCCACCCTTCCCGTTGCAGTCCCTGATGCAGGCTCCCCTCCTGATC A T GM2A Ensembl:ENSG00000196743 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151253144..151259809 26863196 MeRIP-seq:(Medium) rs1400709234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788993,Human_RBP_ID_4846105,Human_RBP_ID_17415402,Human_RBP_ID_18956763,Human_RBP_ID_27513042 Human_Splice_Rec_712017 82911 RMVar_ID_82911 Human_SNP_ID_256392584 m1A Human chr5 - 151253227 151253227 151253227 AGCCCAGGGCGATCAGGAGGGGAGCCTGCATCAGGGACTGCATCGGGAAGGGTGGGTCAGGGCGG AGCCCAGGGCGATCAGGAGGGGAGCCTGCATCGGGGACTGCATCGGGAAGGGTGGGTCAGGGCGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:151253147..151253275 26863410 MeRIP-seq:(Medium) rs762676667 Functional Loss SNV dbSNP153 33..33 33 - - - 82912 RMVar_ID_82912 Human_SNP_ID_256392624 m1A Human chr5 + 151253296 151253296 151253296 TCTCGCGGCCCCTGCGCAAGCCCACCTGAAAAAGGTGAGTGCACCCTCTTTTAAGAGTCTGTTTG TCTCGCGGCCCCTGCGCAAGCCCACCTGAAAAGGGTGAGTGCACCCTCTTTTAAGAGTCTGTTTG A G GM2A Ensembl:ENSG00000196743 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151253247..151259805 32194978 MeRIP-seq:(Medium) rs909177693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_712017 82913 RMVar_ID_82913 Human_SNP_ID_256394100 m1A Human chr5 + 151259848 151259848 151259848 TCAGAAGCCTGACTCTGGAGCCTGACCCCATCATCGTTCCTGGAAATGTGACCCTCAGTGTCATG TCAGAAGCCTGACTCTGGAGCCTGACCCCATCGTCGTTCCTGGAAATGTGACCCTCAGTGTCATG A G GM2A Ensembl:ENSG00000196743 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs153477 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5509103,Human_RBP_ID_22459345,Human_RBP_ID_22771488,Human_RBP_ID_24091380 Human_Splice_Rec_712014,Human_Splice_Rec_712015,Human_Splice_Rec_712018,Human_Splice_Rec_712019,Human_Splice_Rec_712023 Clinvar_Rec_429 GWAS_ID_10017,GWAS_ID_10018,GWAS_ID_10019,GWAS_ID_10020,GWAS_ID_10021,GWAS_ID_10022,GWAS_ID_10023,GWAS_ID_10024,GWAS_ID_10025,GWAS_ID_10026,GWAS_ID_10027,GWAS_ID_10028,GWAS_ID_10029,GWAS_ID_10030,GWAS_ID_10031,GWAS_ID_10032,GWAS_ID_10033,GWAS_ID_10034,GWAS_ID_10035,GWAS_ID_10036,GWAS_ID_10037 82914 RMVar_ID_82914 Human_SNP_ID_256394112 m1A Human chr5 + 151259878 151259878 151259878 TCATCGTTCCTGGAAATGTGACCCTCAGTGTCATGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT TCATCGTTCCTGGAAATGTGACCCTCAGTGTCGTGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT A G GM2A Ensembl:ENSG00000196743 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs153478 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22459005,Human_RBP_ID_22771489 Human_Splice_Rec_712015,Human_Splice_Rec_712019,Human_Splice_Rec_712023 Clinvar_Rec_430 GWAS_ID_10038,GWAS_ID_10039,GWAS_ID_10040,GWAS_ID_10041,GWAS_ID_10042,GWAS_ID_10043 82915 RMVar_ID_82915 Human_SNP_ID_256394113 m1A Human chr5 + 151259878 151259878 151259878 TCATCGTTCCTGGAAATGTGACCCTCAGTGTCATGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT TCATCGTTCCTGGAAATGTGACCCTCAGTGTCTTGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT A T GM2A Ensembl:ENSG00000196743 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs153478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22459005,Human_RBP_ID_22771489 Human_Splice_Rec_712015,Human_Splice_Rec_712019,Human_Splice_Rec_712023 Clinvar_Rec_430 GWAS_ID_10038,GWAS_ID_10039,GWAS_ID_10040,GWAS_ID_10041,GWAS_ID_10042,GWAS_ID_10043 82916 RMVar_ID_82916 Human_SNP_ID_256395930 m1A Human chr5 + 151267603 151267603 151267603 TCCACTACCCTCACTGAAAATCATTTTGTACCACTTACATTTTAGGCTGGGGCAAGCAGCCCTGA TCCACTACCCTCACTGAAAATCATTTTGTACCCCTTACATTTTAGGCTGGGGCAAGCAGCCCTGA A C GM2A Ensembl:ENSG00000196743 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151267553..151267753 32194978 MeRIP-seq:(Medium) rs1163705339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15354163,Human_RBP_ID_17298868,Human_RBP_ID_17412396,Human_RBP_ID_17528369,Human_RBP_ID_18355361 Human_miRNA_ID_284629 82917 RMVar_ID_82917 Human_SNP_ID_256396068 m1A Human chr5 - 151268101 151268101 151268101 AACATGTTTCTCACGGTTCTTATCAGTCATTTAAGTCTCTTGCTAGGCCCTGCGGGTACCTGAGT AACATGTTTCTCACGGTTCTTATCAGTCATTTGAGTCTCTTGCTAGGCCCTGCGGGTACCTGAGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151268051..151268151 32194978 MeRIP-seq:(Medium) rs959917074 Functional Loss SNV dbSNP153 33..33 33 - - - 82918 RMVar_ID_82918 Human_SNP_ID_256396069 m1A Human chr5 - 151268101 151268101 151268101 AACATGTTTCTCACGGTTCTTATCAGTCATTTAAGTCTCTTGCTAGGCCCTGCGGGTACCTGAGT AACATGTTTCTCACGGTTCTTATCAGTCATTTCAGTCTCTTGCTAGGCCCTGCGGGTACCTGAGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151268051..151268151 32194978 MeRIP-seq:(Medium) rs959917074 Functional Loss SNV dbSNP153 33..33 33 - - - 82919 RMVar_ID_82919 Human_SNP_ID_256495864 m1A Human chr5 + 151669751 151669751 151669751 CAGGGTGCACTTTGTGGCAAAGAAGTGGCAGGAAGAGTCGAAGGTCTTGTTGTCATTGCTGCACA CAGGGTGCACTTTGTGGCAAAGAAGTGGCAGGGAGAGTCGAAGGTCTTGTTGTCATTGCTGCACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151667637..151669800 32194978 MeRIP-seq:(Medium) rs750310326 Functional Loss SNV dbSNP153 33..33 33 - - - 82920 RMVar_ID_82920 Human_SNP_ID_256496284 m1A Human chr5 - 151671556 151671554 151671556 TGGCGAGTTTGAGAAGGTGAGGGCTGAGAGACAGGGGCAGGGGGAAGGGATTGGGCACTTCGGAA TGGCGAGTTTGAGAAGGTGAGGGCTGAGAGAC__GGGCAGGGGGAAGGGATTGGGCACTTCGGAA CCT C SPARC Ensembl:ENSG00000113140 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151671551..151671625 32194978 MeRIP-seq:(Medium) rs772924854 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_102158,RMVar_hsa_circ_235592,RMVar_hsa_circ_107924,RMVar_hsa_circ_84647,RMVar_hsa_circ_235597,RMVar_hsa_circ_120704,RMVar_hsa_circ_235598,RMVar_hsa_circ_103854,RMVar_hsa_circ_118762,RMVar_hsa_circ_102976,RMVar_hsa_circ_235604,RMVar_hsa_circ_235605,RMVar_hsa_circ_235606,RMVar_hsa_circ_235603,RMVar_hsa_circ_347507,RMVar_hsa_circ_235608,RMVar_hsa_circ_118422 82921 RMVar_ID_82921 Human_SNP_ID_256496287 m1A Human chr5 - 151671556 151671556 151671556 TGGCGAGTTTGAGAAGGTGAGGGCTGAGAGACAGGGGCAGGGGGAAGGGATTGGGCACTTCGGAA TGGCGAGTTTGAGAAGGTGAGGGCTGAGAGACCGGGGCAGGGGGAAGGGATTGGGCACTTCGGAA T G SPARC Ensembl:ENSG00000113140 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151671551..151671625 32194978 MeRIP-seq:(Medium) rs755652481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102158,RMVar_hsa_circ_235592,RMVar_hsa_circ_107924,RMVar_hsa_circ_84647,RMVar_hsa_circ_235597,RMVar_hsa_circ_120704,RMVar_hsa_circ_235598,RMVar_hsa_circ_103854,RMVar_hsa_circ_118762,RMVar_hsa_circ_102976,RMVar_hsa_circ_235604,RMVar_hsa_circ_235605,RMVar_hsa_circ_235606,RMVar_hsa_circ_235603,RMVar_hsa_circ_347507,RMVar_hsa_circ_235608,RMVar_hsa_circ_118422 82922 RMVar_ID_82922 Human_SNP_ID_256500092 m1A Human chr5 - 151686855 151686855 151686855 CCGCCTGCCTGCCTGCCACTGAGGTATGTGTGACCCCCGCCCAGCCTTTCCCTTCTATAGTTGCA CCGCCTGCCTGCCTGCCACTGAGGTATGTGTGGCCCCCGCCCAGCCTTTCCCTTCTATAGTTGCA T C SPARC Ensembl:ENSG00000113140 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151686851..151686925 32194978 MeRIP-seq:(Medium) rs764966806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102976,RMVar_hsa_circ_235606,RMVar_hsa_circ_113340,RMVar_hsa_circ_235609 82923 RMVar_ID_82923 Human_SNP_ID_256514131 m1A Human chr5 - 151746323 151746323 151746323 AAAGACTGTTTCCTACCTTGGCCTTGAGTAGCAGGGGCCTGGTCCCCACAGCCCACAGGATGGAC AAAGACTGTTTCCTACCTTGGCCTTGAGTAGCGGGGGCCTGGTCCCCACAGCCCACAGGATGGAC T C ATOX1 Ensembl:ENSG00000177556 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs890328418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_635568,Human_RBP_ID_946493,Human_RBP_ID_5121576,Human_RBP_ID_9172785,Human_RBP_ID_17662771,Human_RBP_ID_18210459,Human_RBP_ID_22459847,Human_RBP_ID_26352805 Human_Splice_Rec_712461,Human_Splice_Rec_712465,Human_Splice_Rec_712471,Human_Splice_Rec_712477,Human_Splice_Rec_712485 Human_miRNA_ID_1420914,Human_miRNA_ID_2725157 RMVar_hsa_circ_69570,RMVar_hsa_circ_92569,RMVar_hsa_circ_114971,RMVar_hsa_circ_235615,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 82924 RMVar_ID_82924 Human_SNP_ID_256514132 m1A Human chr5 - 151746323 151746323 151746323 AAAGACTGTTTCCTACCTTGGCCTTGAGTAGCAGGGGCCTGGTCCCCACAGCCCACAGGATGGAC AAAGACTGTTTCCTACCTTGGCCTTGAGTAGCCGGGGCCTGGTCCCCACAGCCCACAGGATGGAC T G ATOX1 Ensembl:ENSG00000177556 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_635568,Human_RBP_ID_946493,Human_RBP_ID_5121576,Human_RBP_ID_9172785,Human_RBP_ID_17662771,Human_RBP_ID_18210459,Human_RBP_ID_22459847,Human_RBP_ID_26352805 Human_Splice_Rec_712461,Human_Splice_Rec_712465,Human_Splice_Rec_712471,Human_Splice_Rec_712477,Human_Splice_Rec_712485 Human_miRNA_ID_1420914,Human_miRNA_ID_2725157 RMVar_hsa_circ_69570,RMVar_hsa_circ_92569,RMVar_hsa_circ_114971,RMVar_hsa_circ_235615,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 82925 RMVar_ID_82925 Human_SNP_ID_256514168 m1A Human chr5 - 151746423 151746423 151746423 CTGCAGGAGTTAAGTATGACATTGACCTGCCCAACAAGAAGGTCTGCATTGAATCTGAGCACAGC CTGCAGGAGTTAAGTATGACATTGACCTGCCCGACAAGAAGGTCTGCATTGAATCTGAGCACAGC T C ATOX1 Ensembl:ENSG00000177556 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr5:151746376..151746500;chr5:151746376..151746475 26863196,32194978 MeRIP-seq:(Medium) rs1023307721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_635572,Human_RBP_ID_1648443,Human_RBP_ID_1990644,Human_RBP_ID_5121576,Human_RBP_ID_17662999,Human_RBP_ID_18202120,Human_RBP_ID_24091574 Human_Splice_Rec_712460,Human_Splice_Rec_712464,Human_Splice_Rec_712470,Human_Splice_Rec_712476,Human_Splice_Rec_712484,Human_Splice_Rec_712490 RMVar_hsa_circ_69570,RMVar_hsa_circ_92569,RMVar_hsa_circ_114971,RMVar_hsa_circ_235615,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 82926 RMVar_ID_82926 Human_SNP_ID_256515530 m1A Human chr5 - 151751705 151751705 151751705 GAAGCTGTCTCTCGGGTCCTCAATAAGCTTGGAGGTGAGTGAGTGGCCCTGAGTTGGGTGCACTT GAAGCTGTCTCTCGGGTCCTCAATAAGCTTGGGGGTGAGTGAGTGGCCCTGAGTTGGGTGCACTT T C ATOX1 Ensembl:ENSG00000177556 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr5:151751701..151751846;chr5:151751701..151751800 26863410,32194978 MeRIP-seq:(Medium) rs994624158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846108,Human_RBP_ID_19124883 Human_Splice_Rec_712458,Human_Splice_Rec_712459,Human_Splice_Rec_712463,Human_Splice_Rec_712468,Human_Splice_Rec_712469,Human_Splice_Rec_712474,Human_Splice_Rec_712475,Human_Splice_Rec_712482,Human_Splice_Rec_712483,Human_Splice_Rec_712488,Human_Splice_Rec_712489 RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 82927 RMVar_ID_82927 Human_SNP_ID_256517164 m1A Human chr5 + 151758595 151758593 151758595 CGGCGGTGTGGCGGCGGTGTGGCGGCGGTGTCAGCAGCGCCTCTCTGGATTCGGAGGGCGGGTTC CGGCGGTGTGGCGGCGGTGTGGCGGCGGTGT__GCAGCGCCTCTCTGGATTCGGAGGGCGGGTTC TCA T AC091982.1 Ensembl:ENSG00000253921 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:151758480..151758625 26863196 MeRIP-seq:(Medium) rs1456017057 Functional Loss DEL dbSNP153 32..33 33 - - - 82928 RMVar_ID_82928 Human_SNP_ID_256521073 m1A Human chr5 + 151771983 151771983 151771983 TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTACTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTCCTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC A C G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2915874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75800,Human_RBP_ID_635578,Human_RBP_ID_788038,Human_RBP_ID_1039972,Human_RBP_ID_1211436,Human_RBP_ID_1648445,Human_RBP_ID_1990646,Human_RBP_ID_4818450,Human_RBP_ID_5477120,Human_RBP_ID_7406746,Human_RBP_ID_8607840,Human_RBP_ID_8886736,Human_RBP_ID_9306796,Human_RBP_ID_9335416,Human_RBP_ID_17707393,Human_RBP_ID_18057401,Human_RBP_ID_18425036,Human_RBP_ID_18448380,Human_RBP_ID_18836607,Human_RBP_ID_21900800,Human_RBP_ID_26530702,Human_RBP_ID_27076633,Human_RBP_ID_27333259 Human_Splice_Rec_712509,Human_Splice_Rec_712531,Human_Splice_Rec_712553,Human_Splice_Rec_712555,Human_Splice_Rec_712561,Human_Splice_Rec_712571,Human_Splice_Rec_712579,Human_Splice_Rec_712587,Human_Splice_Rec_712607 Human_miRNA_ID_1955339,Human_miRNA_ID_2055165,Human_miRNA_ID_2501914 GWAS_ID_10044,GWAS_ID_10045,GWAS_ID_10046,GWAS_ID_10047,GWAS_ID_10048,GWAS_ID_10049,GWAS_ID_10050,GWAS_ID_10051,GWAS_ID_10052,GWAS_ID_10053,GWAS_ID_10054,GWAS_ID_10055,GWAS_ID_10056,GWAS_ID_10057,GWAS_ID_10058,GWAS_ID_10059,GWAS_ID_10060,GWAS_ID_10061,GWAS_ID_10062,GWAS_ID_10063,GWAS_ID_10064,GWAS_ID_10065,GWAS_ID_10066,GWAS_ID_10067,GWAS_ID_10068,GWAS_ID_10069 RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619 82929 RMVar_ID_82929 Human_SNP_ID_256521074 m1A Human chr5 + 151771983 151771983 151771983 TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTACTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTGCTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC A G G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2915874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75800,Human_RBP_ID_635578,Human_RBP_ID_788038,Human_RBP_ID_1039972,Human_RBP_ID_1211436,Human_RBP_ID_1648445,Human_RBP_ID_1990646,Human_RBP_ID_4818450,Human_RBP_ID_5477120,Human_RBP_ID_7406746,Human_RBP_ID_8607840,Human_RBP_ID_8886736,Human_RBP_ID_9306796,Human_RBP_ID_9335416,Human_RBP_ID_17707393,Human_RBP_ID_18057401,Human_RBP_ID_18425036,Human_RBP_ID_18448380,Human_RBP_ID_18836607,Human_RBP_ID_21900800,Human_RBP_ID_26530702,Human_RBP_ID_27076633,Human_RBP_ID_27333259 Human_Splice_Rec_712509,Human_Splice_Rec_712531,Human_Splice_Rec_712553,Human_Splice_Rec_712555,Human_Splice_Rec_712561,Human_Splice_Rec_712571,Human_Splice_Rec_712579,Human_Splice_Rec_712587,Human_Splice_Rec_712607 Human_miRNA_ID_1955339,Human_miRNA_ID_2055165,Human_miRNA_ID_2501914 GWAS_ID_10044,GWAS_ID_10045,GWAS_ID_10046,GWAS_ID_10047,GWAS_ID_10048,GWAS_ID_10049,GWAS_ID_10050,GWAS_ID_10051,GWAS_ID_10052,GWAS_ID_10053,GWAS_ID_10054,GWAS_ID_10055,GWAS_ID_10056,GWAS_ID_10057,GWAS_ID_10058,GWAS_ID_10059,GWAS_ID_10060,GWAS_ID_10061,GWAS_ID_10062,GWAS_ID_10063,GWAS_ID_10064,GWAS_ID_10065,GWAS_ID_10066,GWAS_ID_10067,GWAS_ID_10068,GWAS_ID_10069 RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619 82930 RMVar_ID_82930 Human_SNP_ID_256521075 m1A Human chr5 + 151771983 151771983 151771983 TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTACTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTTCTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC A T G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2915874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75800,Human_RBP_ID_635578,Human_RBP_ID_788038,Human_RBP_ID_1039972,Human_RBP_ID_1211436,Human_RBP_ID_1648445,Human_RBP_ID_1990646,Human_RBP_ID_4818450,Human_RBP_ID_5477120,Human_RBP_ID_7406746,Human_RBP_ID_8607840,Human_RBP_ID_8886736,Human_RBP_ID_9306796,Human_RBP_ID_9335416,Human_RBP_ID_17707393,Human_RBP_ID_18057401,Human_RBP_ID_18425036,Human_RBP_ID_18448380,Human_RBP_ID_18836607,Human_RBP_ID_21900800,Human_RBP_ID_26530702,Human_RBP_ID_27076633,Human_RBP_ID_27333259 Human_Splice_Rec_712509,Human_Splice_Rec_712531,Human_Splice_Rec_712553,Human_Splice_Rec_712555,Human_Splice_Rec_712561,Human_Splice_Rec_712571,Human_Splice_Rec_712579,Human_Splice_Rec_712587,Human_Splice_Rec_712607 Human_miRNA_ID_1955339,Human_miRNA_ID_2055165,Human_miRNA_ID_2501914 GWAS_ID_10044,GWAS_ID_10045,GWAS_ID_10046,GWAS_ID_10047,GWAS_ID_10048,GWAS_ID_10049,GWAS_ID_10050,GWAS_ID_10051,GWAS_ID_10052,GWAS_ID_10053,GWAS_ID_10054,GWAS_ID_10055,GWAS_ID_10056,GWAS_ID_10057,GWAS_ID_10058,GWAS_ID_10059,GWAS_ID_10060,GWAS_ID_10061,GWAS_ID_10062,GWAS_ID_10063,GWAS_ID_10064,GWAS_ID_10065,GWAS_ID_10066,GWAS_ID_10067,GWAS_ID_10068,GWAS_ID_10069 RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619 82931 RMVar_ID_82931 Human_SNP_ID_256521103 m1A Human chr5 + 151772027 151772027 151772027 GCTGTGGTGCAGAGCTAGTTCCTCTCCAGCTCAGCCGCGTAGGTACGCCGGGGTGTGGGCGGGGC GCTGTGGTGCAGAGCTAGTTCCTCTCCAGCTCGGCCGCGTAGGTACGCCGGGGTGTGGGCGGGGC A G G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151771976..151772050 32194978 MeRIP-seq:(Medium) rs747396632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946761,Human_RBP_ID_1211437,Human_RBP_ID_1648446,Human_RBP_ID_4846111,Human_RBP_ID_5151692,Human_RBP_ID_5397611,Human_RBP_ID_5449479,Human_RBP_ID_5477121,Human_RBP_ID_8607841,Human_RBP_ID_8893806,Human_RBP_ID_9335416,Human_RBP_ID_18042578,Human_RBP_ID_18425037,Human_RBP_ID_18465259,Human_RBP_ID_19126635,Human_RBP_ID_22460266 Human_Splice_Rec_712509,Human_Splice_Rec_712531,Human_Splice_Rec_712553,Human_Splice_Rec_712555,Human_Splice_Rec_712561,Human_Splice_Rec_712571,Human_Splice_Rec_712579,Human_Splice_Rec_712587,Human_Splice_Rec_712607 RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619 82932 RMVar_ID_82932 Human_SNP_ID_256521109 m1A Human chr5 - 151772034 151772034 151772034 CCTCCCTGCCCCGCCCACACCCCGGCGTACCTACGCGGCTGAGCTGGAGAGGAACTAGCTCTGCA CCTCCCTGCCCCGCCCACACCCCGGCGTACCTGCGCGGCTGAGCTGGAGAGGAACTAGCTCTGCA T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:151771951..151772075;chr5:151772003..151772094;chr5:151772004..151772108 26863410,26863196,26863196 MeRIP-seq:(Medium) rs549558936 Functional Loss SNV dbSNP153 33..33 33 - - - 82933 RMVar_ID_82933 Human_SNP_ID_256526282 m1A Human chr5 + 151790898 151790898 151790898 ATTATTATTATTATTTTTTTAAGGAAATCCACAGGAAAGTGATGTCACAAAACTTCACCAACTGC ATTATTATTATTATTTTTTTAAGGAAATCCACGGGAAAGTGATGTCACAAAACTTCACCAACTGC A G G3BP1 Ensembl:ENSG00000145907 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151790876..151790950 32194978 MeRIP-seq:(Medium) rs1422157510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839756,Human_RBP_ID_943107,Human_RBP_ID_1648480,Human_RBP_ID_1990693,Human_RBP_ID_3763065,Human_RBP_ID_9398577,Human_RBP_ID_18836630,Human_RBP_ID_25933397,Human_RBP_ID_27333265 Human_Splice_Rec_712502,Human_Splice_Rec_712508,Human_Splice_Rec_712514,Human_Splice_Rec_712536,Human_Splice_Rec_712560,Human_Splice_Rec_712568,Human_Splice_Rec_712574,Human_Splice_Rec_712584,Human_Splice_Rec_712592,Human_Splice_Rec_712612,Human_Splice_Rec_712634,Human_Splice_Rec_712638,Human_Splice_Rec_712646 Human_miRNA_ID_2721572,Human_miRNA_ID_3066920 RMVar_hsa_circ_10319,RMVar_hsa_circ_84068,RMVar_hsa_circ_81022,RMVar_hsa_circ_235619,RMVar_hsa_circ_275819,RMVar_hsa_circ_293465,RMVar_hsa_circ_331186,RMVar_hsa_circ_298406,RMVar_hsa_circ_276184,RMVar_hsa_circ_115515,RMVar_hsa_circ_271413,RMVar_hsa_circ_101706,RMVar_hsa_circ_235623,RMVar_hsa_circ_235627,RMVar_hsa_circ_77316,RMVar_hsa_circ_235629,RMVar_hsa_circ_235628,RMVar_hsa_circ_235625,RMVar_hsa_circ_235626,RMVar_hsa_circ_235624,RMVar_hsa_circ_235621,RMVar_hsa_circ_235622,RMVar_hsa_circ_309286,RMVar_hsa_circ_321849,RMVar_hsa_circ_322634,RMVar_hsa_circ_310132,RMVar_hsa_circ_108310,RMVar_hsa_circ_235635,RMVar_hsa_circ_290922,RMVar_hsa_circ_325996,RMVar_hsa_circ_355892,RMVar_hsa_circ_235631,RMVar_hsa_circ_353443,RMVar_hsa_circ_291580,RMVar_hsa_circ_278520,RMVar_hsa_circ_278825,RMVar_hsa_circ_235636,RMVar_hsa_circ_235633,RMVar_hsa_circ_235634,RMVar_hsa_circ_235632,RMVar_hsa_circ_235637,RMVar_hsa_circ_63148 82934 RMVar_ID_82934 Human_SNP_ID_256528886 m1A Human chr5 - 151800203 151800203 151800203 GCTCACCAGCCTCACGGACTTAAAAGGAGACAAAAACATCAATGAAAGACAAGAGAAAGAAGACA GCTCACCAGCCTCACGGACTTAAAAGGAGACAGAAACATCAATGAAAGACAAGAGAAAGAAGACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151800201..151800275 32194978 MeRIP-seq:(Medium) rs1294076191 Functional Loss SNV dbSNP153 33..33 33 - - - 82935 RMVar_ID_82935 Human_SNP_ID_256529981 m1A Human chr5 + 151803950 151803950 151803950 GTCGAAGAGAAGAAGACTCGAGCTGCCAGGGAAGGCGACCGACGAGATAATCGCCTTCGGGGACC GTCGAAGAGAAGAAGACTCGAGCTGCCAGGGATGGCGACCGACGAGATAATCGCCTTCGGGGACC A T G3BP1 Ensembl:ENSG00000145907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:151803901..151804080 26863196 MeRIP-seq:(Medium) rs770560655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250189,Human_RBP_ID_635596,Human_RBP_ID_946780,Human_RBP_ID_1648519,Human_RBP_ID_1990731,Human_RBP_ID_7407036,Human_RBP_ID_8893808,Human_RBP_ID_9398589,Human_RBP_ID_15355695,Human_RBP_ID_22460282,Human_RBP_ID_23116281,Human_RBP_ID_24548150 Human_Splice_Rec_712530,Human_Splice_Rec_712552,Human_Splice_Rec_712606,Human_Splice_Rec_712628 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235631,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 82936 RMVar_ID_82936 Human_SNP_ID_256530007 m1A Human chr5 + 151804038 151804038 151804038 GTGGTGGAATGAGAGGCCCTCCCCGTGGAGGCATGGTGCAGAAACCAGGATTTGGAGTGGGAAGG GTGGTGGAATGAGAGGCCCTCCCCGTGGAGGCTTGGTGCAGAAACCAGGATTTGGAGTGGGAAGG A T G3BP1 Ensembl:ENSG00000145907 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:151803949..151804071 26863196 MeRIP-seq:(Medium) rs193159435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250189,Human_RBP_ID_635599,Human_RBP_ID_839063,Human_RBP_ID_946781,Human_RBP_ID_7407039,Human_RBP_ID_8607905,Human_RBP_ID_9354548,Human_RBP_ID_15355703,Human_RBP_ID_22459357,Human_RBP_ID_22615317,Human_RBP_ID_24091707,Human_RBP_ID_24385664 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 82937 RMVar_ID_82937 Human_SNP_ID_257140020 m1A Human chr5 - 154294771 154294771 154294771 CAAAAACTATGAAAAATAGAAAAGGGCAAATCAGTAACACAGGCCCAGGAGTTACACTGCCTAAG CAAAAACTATGAAAAATAGAAAAGGGCAAATCTGTAACACAGGCCCAGGAGTTACACTGCCTAAG T A RF00017-4483,RF00017-4490 RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154294769..154294877 26863196 MeRIP-seq:(Medium) rs772523857 Functional Loss SNV dbSNP153 33..33 33 - - - 82938 RMVar_ID_82938 Human_SNP_ID_257140021 m1A Human chr5 - 154294771 154294771 154294771 CAAAAACTATGAAAAATAGAAAAGGGCAAATCAGTAACACAGGCCCAGGAGTTACACTGCCTAAG CAAAAACTATGAAAAATAGAAAAGGGCAAATCCGTAACACAGGCCCAGGAGTTACACTGCCTAAG T G RF00017-4483,RF00017-4490 RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154294769..154294877 26863196 MeRIP-seq:(Medium) rs772523857 Functional Loss SNV dbSNP153 33..33 33 - - - 82939 RMVar_ID_82939 Human_SNP_ID_257173816 m1A Human chr5 + 154446036 154446036 154446036 GGAGCGTTCGGCGGGCGGCGGCCGGGCGGCCCAGGGGCTGCCGCGGGACTCGGGGCGCAGCCGAG GGAGCGTTCGGCGGGCGGCGGCCGGGCGGCCCCGGGGCTGCCGCGGGACTCGGGGCGCAGCCGAG A C SAP30L Ensembl:ENSG00000164576 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154445988..154446743 26863196 MeRIP-seq:(Medium) rs892734215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788908,Human_RBP_ID_4818986,Human_RBP_ID_9306797 82940 RMVar_ID_82940 Human_SNP_ID_257173937 m1A Human chr5 - 154446365 154446365 154446365 TCGAGGCCCCGGGGTCGGCTCCCGCGGCTCGCAGGGCCCCGCCGGGGGTCACCCGGAGGAGCCTT TCGAGGCCCCGGGGTCGGCTCCCGCGGCTCGCGGGGCCCCGCCGGGGGTCACCCGGAGGAGCCTT T C RF00017-4483,RF00017-4490 RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:154446088..154446625 26863196 MeRIP-seq:(Medium) rs1227951542 Functional Loss SNV dbSNP153 33..33 33 - - - 82941 RMVar_ID_82941 Human_SNP_ID_257173972 m1A Human chr5 - 154446454 154446454 154446454 CAGCCCGGGCGCTGCCCTGCCCCGCGTCCGAGAGGCCCGGCTCCCTCGGCCCCCGGCCCTCCGCC CAGCCCGGGCGCTGCCCTGCCCCGCGTCCGAGCGGCCCGGCTCCCTCGGCCCCCGGCCCTCCGCC T G RF00017-4483,RF00017-4490 RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:154446353..154446454 26863410 MeRIP-seq:(Medium) rs111697397 Functional Loss SNV dbSNP153 33..33 33 - - - 82942 RMVar_ID_82942 Human_SNP_ID_257174029 m1A Human chr5 + 154446624 154446621 154446624 CCGGGGCGGGGAGATGAACGGCTTCAGCACGGAGGAGGACAGCCGCGAAGGGCCCCCCGCCGCCC CCGGGGCGGGGAGATGAACGGCTTCAGCAC___GGAGGACAGCCGCGAAGGGCCCCCCGCCGCCC CGGA C SAP30L Ensembl:ENSG00000164576 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154445976..154446800 26863196 MeRIP-seq:(Medium) rs1461676520 Functional Loss DEL dbSNP153 31..33 33 - - - 82943 RMVar_ID_82943 Human_SNP_ID_257174040 m1A Human chr5 + 154446640 154446640 154446640 AACGGCTTCAGCACGGAGGAGGACAGCCGCGAAGGGCCCCCCGCCGCCCCAGCTGCCGCCGCCCC AACGGCTTCAGCACGGAGGAGGACAGCCGCGACGGGCCCCCCGCCGCCCCAGCTGCCGCCGCCCC A C SAP30L Ensembl:ENSG00000164576 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:154446552..154446652 26863410 MeRIP-seq:(Medium) rs755763544 Functional Loss SNV dbSNP153 33..33 33 - - - 82944 RMVar_ID_82944 Human_SNP_ID_257209534 m1A Human chr5 + 154587264 154587261 154587265 AACCAGGGAGTTGGAGAAAGAAAGAAAGTTAGAAAGAAGGAAAGAAGAAAGAAAGAAGGAAAGAA AACCAGGGAGTTGGAGAAAGAAAGAAAGTT____AGAAGGAAAGAAGAAAGAAAGAAGGAAAGAA TAGAA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154587258..154587369 26863196 MeRIP-seq:(Medium) rs909846411 Functional Loss DEL dbSNP153 31..34 33 - - - 82945 RMVar_ID_82945 Human_SNP_ID_257233484 m1A Human chr5 - 154682810 154682810 154682810 GAAAGAGGAAAGGGGGAGAGGAGACGGGGGAGAGGCGGAGGTGGGAGGGGGCAGTTCGAAGCCCC GAAAGAGGAAAGGGGGAGAGGAGACGGGGGAGGGGCGGAGGTGGGAGGGGGCAGTTCGAAGCCCC T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:154682740..154682831 26863410 MeRIP-seq:(Medium) rs1449461342 Functional Loss SNV dbSNP153 33..33 33 - - - 82946 RMVar_ID_82946 Human_SNP_ID_257250596 m1A Human chr5 - 154755388 154755388 154755388 GGGCGGCCCGGGCTTCCCGGCTCGGGGGCTGCAGCAATATGGACGGACGGGGGAGAGGCGCGGCG GGGCGGCCCGGGCTTCCCGGCTCGGGGGCTGCGGCAATATGGACGGACGGGGGAGAGGCGCGGCG T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154755338..154755422 26863196 MeRIP-seq:(Medium) rs1366759751 Functional Loss SNV dbSNP153 33..33 33 - - - 82947 RMVar_ID_82947 Human_SNP_ID_257250648 m1A Human chr5 + 154755505 154755505 154755505 GGGGGCGTCTTGCGAGGAACGGGCGGGGGGGGACGCACGCCTAGGAGGCCTGGACTGCAGAGTGG GGGGGCGTCTTGCGAGGAACGGGCGGGGGGGGCCGCACGCCTAGGAGGCCTGGACTGCAGAGTGG A C LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:154755376..154755625;chr5:154755426..154755602 26863196 MeRIP-seq:(Medium) rs1295055629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76041,Human_RBP_ID_250240,Human_RBP_ID_788161,Human_RBP_ID_840007,Human_RBP_ID_3784269,Human_RBP_ID_3967574,Human_RBP_ID_4819091,Human_RBP_ID_5326615,Human_RBP_ID_7408219,Human_RBP_ID_8136978,Human_RBP_ID_8893814,Human_RBP_ID_9306801,Human_RBP_ID_9335421,Human_RBP_ID_9354609,Human_RBP_ID_9436772,Human_RBP_ID_18956227,Human_RBP_ID_22459859,Human_RBP_ID_22613675,Human_RBP_ID_26792192,Human_RBP_ID_27076801,Human_RBP_ID_27513182 RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_101061,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235698 82948 RMVar_ID_82948 Human_SNP_ID_257250649 m1A Human chr5 + 154755505 154755505 154755505 GGGGGCGTCTTGCGAGGAACGGGCGGGGGGGGACGCACGCCTAGGAGGCCTGGACTGCAGAGTGG GGGGGCGTCTTGCGAGGAACGGGCGGGGGGGGGCGCACGCCTAGGAGGCCTGGACTGCAGAGTGG A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:154755376..154755625;chr5:154755426..154755602 26863196 MeRIP-seq:(Medium) rs1295055629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76041,Human_RBP_ID_250240,Human_RBP_ID_788161,Human_RBP_ID_840007,Human_RBP_ID_3784269,Human_RBP_ID_3967574,Human_RBP_ID_4819091,Human_RBP_ID_5326615,Human_RBP_ID_7408219,Human_RBP_ID_8136978,Human_RBP_ID_8893814,Human_RBP_ID_9306801,Human_RBP_ID_9335421,Human_RBP_ID_9354609,Human_RBP_ID_9436772,Human_RBP_ID_18956227,Human_RBP_ID_22459859,Human_RBP_ID_22613675,Human_RBP_ID_26792192,Human_RBP_ID_27076801,Human_RBP_ID_27513182 RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_101061,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235698 82949 RMVar_ID_82949 Human_SNP_ID_257259731 m1A Human chr5 + 154790377 154790377 154790377 GTGGTGAGGGCAGCTGTTCCTAAACAGCGCAAAGGCAGCAAGGTAAAGAATAACAGTGGGCAACC GTGGTGAGGGCAGCTGTTCCTAAACAGCGCAAGGGCAGCAAGGTAAAGAATAACAGTGGGCAACC A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154790284..154790435 26863196 MeRIP-seq:(Medium) rs1455024390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967576,Human_RBP_ID_5396320,Human_RBP_ID_8893820 Human_Splice_Rec_713472,Human_Splice_Rec_713473,Human_Splice_Rec_713508,Human_Splice_Rec_713509,Human_Splice_Rec_713534,Human_Splice_Rec_713535,Human_Splice_Rec_713542,Human_Splice_Rec_713543,Human_Splice_Rec_713556,Human_Splice_Rec_713557,Human_Splice_Rec_713566,Human_Splice_Rec_713567 RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_101061,RMVar_hsa_circ_235701,RMVar_hsa_circ_79212,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235698,RMVar_hsa_circ_117975,RMVar_hsa_circ_235699,RMVar_hsa_circ_235700,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_299458,RMVar_hsa_circ_308494,RMVar_hsa_circ_340952,RMVar_hsa_circ_341945,RMVar_hsa_circ_348062,RMVar_hsa_circ_336714,RMVar_hsa_circ_301566,RMVar_hsa_circ_287674,RMVar_hsa_circ_296163,RMVar_hsa_circ_275640,RMVar_hsa_circ_235703,RMVar_hsa_circ_235705,RMVar_hsa_circ_235706,RMVar_hsa_circ_235704 82950 RMVar_ID_82950 Human_SNP_ID_257259813 m1A Human chr5 - 154790707 154790707 154790707 AACCTGCCTATTCTTCCACACAGACTCACCTGAACACTCTTGTGGGCTATCTCTCCAGGTGTGGG AACCTGCCTATTCTTCCACACAGACTCACCTGCACACTCTTGTGGGCTATCTCTCCAGGTGTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:154790591..154790763;chr5:154790626..154790725 26863196 MeRIP-seq:(Medium) rs1332236184 Functional Loss SNV dbSNP153 33..33 33 - - - 82951 RMVar_ID_82951 Human_SNP_ID_257260564 m1A Human chr5 + 154793698 154793698 154793698 CGCCCCACTCGCCCACCGGAGCCTAGACACATACCTGCCAATCGCGGAGAGATCAAAGGTATGCA CGCCCCACTCGCCCACCGGAGCCTAGACACATCCCTGCCAATCGCGGAGAGATCAAAGGTATGCA A C LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:154793651..154793801 26863196 MeRIP-seq:(Medium) rs766970973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76076,Human_RBP_ID_1040110,Human_RBP_ID_8887049,Human_RBP_ID_9305290,Human_RBP_ID_9398593,Human_RBP_ID_17298998,Human_RBP_ID_26352816 Human_Splice_Rec_713479,Human_Splice_Rec_713515,Human_Splice_Rec_713551,Human_Splice_Rec_713563,Human_Splice_Rec_713573,Human_Splice_Rec_713593,Human_Splice_Rec_713605 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_101061,RMVar_hsa_circ_79212,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235698,RMVar_hsa_circ_235700,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_299458,RMVar_hsa_circ_340952,RMVar_hsa_circ_341945,RMVar_hsa_circ_348062,RMVar_hsa_circ_336714,RMVar_hsa_circ_301566,RMVar_hsa_circ_287674,RMVar_hsa_circ_275640,RMVar_hsa_circ_235705,RMVar_hsa_circ_235706,RMVar_hsa_circ_235704,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_311601,RMVar_hsa_circ_235709,RMVar_hsa_circ_235710,RMVar_hsa_circ_320153,RMVar_hsa_circ_37647,RMVar_hsa_circ_235712 82952 RMVar_ID_82952 Human_SNP_ID_257260582 m1A Human chr5 + 154793730 154793730 154793730 ACCTGCCAATCGCGGAGAGATCAAAGGTATGCACTACCCACTATGGAGGGCCTGGACTTGGGAGA ACCTGCCAATCGCGGAGAGATCAAAGGTATGCGCTACCCACTATGGAGGGCCTGGACTTGGGAGA A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154793727..154793814 26863196 MeRIP-seq:(Medium) rs1183582179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15358804,Human_RBP_ID_19128236 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_79212,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235700,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_299458,RMVar_hsa_circ_340952,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_301566,RMVar_hsa_circ_287674,RMVar_hsa_circ_275640,RMVar_hsa_circ_235705,RMVar_hsa_circ_235706,RMVar_hsa_circ_235704,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_311601,RMVar_hsa_circ_235709,RMVar_hsa_circ_235710,RMVar_hsa_circ_37647 82953 RMVar_ID_82953 Human_SNP_ID_257260673 m1A Human chr5 - 154793924 154793924 154793924 CGTCCACGGCCACGGAAGGAAGCCCGCGCCCCACCAGCCCCATCACTCTTCACACTCGATGTCTC CGTCCACGGCCACGGAAGGAAGCCCGCGCCCCGCCAGCCCCATCACTCTTCACACTCGATGTCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154793901..154793925 26863196 MeRIP-seq:(Medium) rs1279538751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235715 82954 RMVar_ID_82954 Human_SNP_ID_257262619 m1A Human chr5 + 154799924 154799921 154799924 TCGTGCAGTCACCCCAGTGCCAACCAAAACAGAGGAGGTCAGCAACCTAAAGACACTACCCAAGG TCGTGCAGTCACCCCAGTGCCAACCAAAAC___GGAGGTCAGCAACCTAAAGACACTACCCAAGG CAGA C LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:154799901..154799925 26863196 MeRIP-seq:(Medium) rs1207091908 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_76089,Human_RBP_ID_1990942,Human_RBP_ID_17299006,Human_RBP_ID_26826772 Human_Splice_Rec_713488,Human_Splice_Rec_713524,Human_Splice_Rec_713582,Human_Splice_Rec_713600,Human_Splice_Rec_713616,Human_Splice_Rec_713624 Human_miRNA_ID_2948731 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_235696,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_287674,RMVar_hsa_circ_275640,RMVar_hsa_circ_235706,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_235709,RMVar_hsa_circ_82607,RMVar_hsa_circ_124067,RMVar_hsa_circ_100944,RMVar_hsa_circ_235713,RMVar_hsa_circ_235714,RMVar_hsa_circ_368160,RMVar_hsa_circ_99153,RMVar_hsa_circ_33218,RMVar_hsa_circ_235717,RMVar_hsa_circ_235718,RMVar_hsa_circ_56067 82955 RMVar_ID_82955 Human_SNP_ID_257262620 m1A Human chr5 + 154799922 154799922 154799922 CCTCGTGCAGTCACCCCAGTGCCAACCAAAACAGAGGAGGTCAGCAACCTAAAGACACTACCCAA CCTCGTGCAGTCACCCCAGTGCCAACCAAAACGGAGGAGGTCAGCAACCTAAAGACACTACCCAA A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154799598..154800064 26863196 MeRIP-seq:(Medium) rs1471162533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76089,Human_RBP_ID_1040117,Human_RBP_ID_1990942,Human_RBP_ID_17299006,Human_RBP_ID_26826772 Human_Splice_Rec_713488,Human_Splice_Rec_713524,Human_Splice_Rec_713582,Human_Splice_Rec_713600,Human_Splice_Rec_713616,Human_Splice_Rec_713624 Human_miRNA_ID_2948731 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_235696,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_287674,RMVar_hsa_circ_275640,RMVar_hsa_circ_235706,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_235709,RMVar_hsa_circ_82607,RMVar_hsa_circ_124067,RMVar_hsa_circ_100944,RMVar_hsa_circ_235713,RMVar_hsa_circ_235714,RMVar_hsa_circ_368160,RMVar_hsa_circ_99153,RMVar_hsa_circ_33218,RMVar_hsa_circ_235717,RMVar_hsa_circ_235718,RMVar_hsa_circ_56067 82956 RMVar_ID_82956 Human_SNP_ID_257263143 m1A Human chr5 + 154802160 154802160 154802160 TGGAGCAGATGGATGGGCGGAAGAACACCTTCACTGCCTGGTCTGATGAGGAATCTGACTATGAG TGGAGCAGATGGATGGGCGGAAGAACACCTTCGCTGCCTGGTCTGATGAGGAATCTGACTATGAG A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154802073..154802306 26863196 MeRIP-seq:(Medium) rs1190995250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76092,Human_RBP_ID_636002,Human_RBP_ID_1040119,Human_RBP_ID_1648744,Human_RBP_ID_1990947,Human_RBP_ID_4851914,Human_RBP_ID_5532104,Human_RBP_ID_8608254,Human_RBP_ID_8887089,Human_RBP_ID_9305296,Human_RBP_ID_9398603,Human_RBP_ID_15359040,Human_RBP_ID_17299008,Human_RBP_ID_18042967,Human_RBP_ID_18836898,Human_RBP_ID_22099788,Human_RBP_ID_26350562,Human_RBP_ID_26523788,Human_RBP_ID_27333447,Human_RBP_ID_27513198 Human_miRNA_ID_2279364,Human_miRNA_ID_2456749,Human_miRNA_ID_2459426,Human_miRNA_ID_2461661,Human_miRNA_ID_2634316,Human_miRNA_ID_2637003,Human_miRNA_ID_2639660,Human_miRNA_ID_2998057 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_235696,RMVar_hsa_circ_235707,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_275640,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_235709,RMVar_hsa_circ_124067,RMVar_hsa_circ_100944,RMVar_hsa_circ_235713,RMVar_hsa_circ_235714,RMVar_hsa_circ_368160,RMVar_hsa_circ_99153,RMVar_hsa_circ_33218,RMVar_hsa_circ_235718,RMVar_hsa_circ_56067 82957 RMVar_ID_82957 Human_SNP_ID_257263441 m1A Human chr5 + 154803411 154803411 154803411 GGAAGTTCCTCCTGGGCCACCTCGGTTCCAGCAAGGTGAGAAGCAGACACCTGAGATCCTGACAT GGAAGTTCCTCCTGGGCCACCTCGGTTCCAGCGAGGTGAGAAGCAGACACCTGAGATCCTGACAT A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:154803306..154803583 32194978 MeRIP-seq:(Medium) rs1190885920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_636006,Human_RBP_ID_1040122 Human_Splice_Rec_713493,Human_Splice_Rec_713529,Human_Splice_Rec_713587,Human_Splice_Rec_713629 Human_miRNA_ID_174055 RMVar_hsa_circ_65232,RMVar_hsa_circ_235707,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_275640,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_235709,RMVar_hsa_circ_124067,RMVar_hsa_circ_100944,RMVar_hsa_circ_235713,RMVar_hsa_circ_235714,RMVar_hsa_circ_368160,RMVar_hsa_circ_99153,RMVar_hsa_circ_33218,RMVar_hsa_circ_235718,RMVar_hsa_circ_56067,RMVar_hsa_circ_5454,RMVar_hsa_circ_23444,RMVar_hsa_circ_364265,RMVar_hsa_circ_235719 82958 RMVar_ID_82958 Human_SNP_ID_257263521 m1A Human chr5 + 154803644 154803644 154803644 CCACTGTCCCAGAGTCACCAAACTACCGCAACACCAGGACCCCTCGCACTCCCCGGACACCACAG CCACTGTCCCAGAGTCACCAAACTACCGCAACTCCAGGACCCCTCGCACTCCCCGGACACCACAG A T LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154803595..154803692 26863196 MeRIP-seq:(Medium) rs773716145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7408511,Human_RBP_ID_8887116,Human_RBP_ID_9262387,Human_RBP_ID_9306826,Human_RBP_ID_15359073,Human_RBP_ID_17299014,Human_RBP_ID_17412547,Human_RBP_ID_17528538,Human_RBP_ID_26530722,Human_RBP_ID_27513206 Human_miRNA_ID_466618,Human_miRNA_ID_1561769,Human_miRNA_ID_2153036,Human_miRNA_ID_2800911,Human_miRNA_ID_3009040 RMVar_hsa_circ_65232,RMVar_hsa_circ_235707,RMVar_hsa_circ_341945,RMVar_hsa_circ_336714,RMVar_hsa_circ_275640,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_235709,RMVar_hsa_circ_124067,RMVar_hsa_circ_100944,RMVar_hsa_circ_235713,RMVar_hsa_circ_235714,RMVar_hsa_circ_368160,RMVar_hsa_circ_99153,RMVar_hsa_circ_33218,RMVar_hsa_circ_235718,RMVar_hsa_circ_56067,RMVar_hsa_circ_5454,RMVar_hsa_circ_23444,RMVar_hsa_circ_364265,RMVar_hsa_circ_55389,RMVar_hsa_circ_235719 82959 RMVar_ID_82959 Human_SNP_ID_257265659 m1A Human chr5 - 154811612 154811612 154811612 TTACATCTACTCGGAAGTCTTCAAGACGTCGGAATTTGCCGAGGTATTCTTGCAGTTTGGGGTCA TTACATCTACTCGGAAGTCTTCAAGACGTCGGCATTTGCCGAGGTATTCTTGCAGTTTGGGGTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154811564..154811674 26863196 MeRIP-seq:(Medium) rs1466832777 Functional Loss SNV dbSNP153 33..33 33 - - - 82960 RMVar_ID_82960 Human_SNP_ID_257266275 m1A Human chr5 + 154813998 154813998 154813998 GCCCCTCCCAGTCTTCCAGCAGGCCTGCTGCCATGATCAGCCAACCCCCTACACCACCCACCGGC GCCCCTCCCAGTCTTCCAGCAGGCCTGCTGCCGTGATCAGCCAACCCCCTACACCACCCACCGGC A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154813947..154814054 26863196 MeRIP-seq:(Medium) rs1242313959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76114,Human_RBP_ID_1648810,Human_RBP_ID_18836941,Human_RBP_ID_27076918 Human_miRNA_ID_2276372 RMVar_hsa_circ_100944,RMVar_hsa_circ_235714,RMVar_hsa_circ_99153,RMVar_hsa_circ_235718,RMVar_hsa_circ_119763,RMVar_hsa_circ_235720 82961 RMVar_ID_82961 Human_SNP_ID_257266298 m1A Human chr5 + 154814053 154814053 154814053 ACCCACCGGCCAGCCTGTCCGGGAAGATGCCAAATGGACAAGCCAGCACTCGAACACACAGACTT ACCCACCGGCCAGCCTGTCCGGGAAGATGCCACATGGACAAGCCAGCACTCGAACACACAGACTT A C LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154813904..154814233 26863196 MeRIP-seq:(Medium) rs761756581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1648811,Human_RBP_ID_1991002,Human_RBP_ID_5212668,Human_RBP_ID_5610573,Human_RBP_ID_7408608,Human_RBP_ID_8608302,Human_RBP_ID_8887154,Human_RBP_ID_15359325,Human_RBP_ID_17299029,Human_RBP_ID_17412553,Human_RBP_ID_18042993,Human_RBP_ID_18836942,Human_RBP_ID_22297577,Human_RBP_ID_26523800,Human_RBP_ID_27513210 Human_miRNA_ID_417891,Human_miRNA_ID_2773907 RMVar_hsa_circ_100944,RMVar_hsa_circ_235714,RMVar_hsa_circ_99153,RMVar_hsa_circ_235718,RMVar_hsa_circ_119763,RMVar_hsa_circ_235720 82962 RMVar_ID_82962 Human_SNP_ID_257266299 m1A Human chr5 + 154814053 154814053 154814053 ACCCACCGGCCAGCCTGTCCGGGAAGATGCCAAATGGACAAGCCAGCACTCGAACACACAGACTT ACCCACCGGCCAGCCTGTCCGGGAAGATGCCAGATGGACAAGCCAGCACTCGAACACACAGACTT A G LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154813904..154814233 26863196 MeRIP-seq:(Medium) rs761756581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1648811,Human_RBP_ID_1991002,Human_RBP_ID_5212668,Human_RBP_ID_5610573,Human_RBP_ID_7408608,Human_RBP_ID_8608302,Human_RBP_ID_8887154,Human_RBP_ID_15359325,Human_RBP_ID_17299029,Human_RBP_ID_17412553,Human_RBP_ID_18042993,Human_RBP_ID_18836942,Human_RBP_ID_22297577,Human_RBP_ID_26523800,Human_RBP_ID_27513210 Human_miRNA_ID_417891,Human_miRNA_ID_2773907 RMVar_hsa_circ_100944,RMVar_hsa_circ_235714,RMVar_hsa_circ_99153,RMVar_hsa_circ_235718,RMVar_hsa_circ_119763,RMVar_hsa_circ_235720 82963 RMVar_ID_82963 Human_SNP_ID_257266439 m1A Human chr5 + 154814477 154814477 154814477 CCCGAGGCTAGTAGGCTGCAACCCTGGTCCCCACCCCTAACCTCCTGCTCCCCCTCAAGCCAACT CCCGAGGCTAGTAGGCTGCAACCCTGGTCCCCCCCCCTAACCTCCTGCTCCCCCTCAAGCCAACT A C LARP1 Ensembl:ENSG00000155506 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:154814426..154814605 26863196 MeRIP-seq:(Medium) rs1005984050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_636027,Human_RBP_ID_1648818,Human_RBP_ID_5213516,Human_RBP_ID_7408630,Human_RBP_ID_8213728,Human_RBP_ID_15359340,Human_RBP_ID_18836946,Human_RBP_ID_24092309,Human_RBP_ID_25874356,Human_RBP_ID_26530058,Human_RBP_ID_27513226 Human_miRNA_ID_844221,Human_miRNA_ID_1421058,Human_miRNA_ID_1705443,Human_miRNA_ID_2725159 RMVar_hsa_circ_100944,RMVar_hsa_circ_235714,RMVar_hsa_circ_99153,RMVar_hsa_circ_235718,RMVar_hsa_circ_119763,RMVar_hsa_circ_235720 82964 RMVar_ID_82964 Human_SNP_ID_257266619 m1A Human chr5 + 154815134 154815134 154815134 CTGGGCTTGGACTGGCTAGAATCTTTCTCTGGACTGTTGCATGTACAGTGCCTCCATCCTGGAGG CTGGGCTTGGACTGGCTAGAATCTTTCTCTGGGCTGTTGCATGTACAGTGCCTCCATCCTGGAGG A G LARP1 Ensembl:ENSG00000155506 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1205807265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76122,Human_RBP_ID_636046,Human_RBP_ID_1211549,Human_RBP_ID_1648828,Human_RBP_ID_1991020,Human_RBP_ID_3763463,Human_RBP_ID_5121447,Human_RBP_ID_5151500,Human_RBP_ID_8213742,Human_RBP_ID_8887176,Human_RBP_ID_15359370,Human_RBP_ID_17299039,Human_RBP_ID_17412564,Human_RBP_ID_17528567,Human_RBP_ID_18355691,Human_RBP_ID_18836953,Human_RBP_ID_21141566,Human_RBP_ID_21900809,Human_RBP_ID_22097284,Human_RBP_ID_24092317,Human_RBP_ID_24504807,Human_RBP_ID_26523835,Human_RBP_ID_27076943,Human_RBP_ID_27333478,Human_RBP_ID_27513240 Human_miRNA_ID_229199,Human_miRNA_ID_592042,Human_miRNA_ID_1330199,Human_miRNA_ID_1605807,Human_miRNA_ID_1680062,Human_miRNA_ID_2025923,Human_miRNA_ID_2215565,Human_miRNA_ID_2656571,Human_miRNA_ID_2729238,Human_miRNA_ID_2824362,Human_miRNA_ID_2858333 RMVar_hsa_circ_100944,RMVar_hsa_circ_235714,RMVar_hsa_circ_99153,RMVar_hsa_circ_235718,RMVar_hsa_circ_119763,RMVar_hsa_circ_235720 82965 RMVar_ID_82965 Human_SNP_ID_257268706 m1A Human chr5 - 154823483 154823482 154823484 CTTCCTCTATCCCTTCCTCAAATGGTGGAGAGACCCCTGCCGCCGTGAGCTACCCACCTTCCACT CTTCCTCTATCCCTTCCTCAAATGGTGGAGA__CCCCTGCCGCCGTGAGCTACCCACCTTCCACT GTC G FAXDC2 Ensembl:ENSG00000170271 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154823442..154823507 26863196 MeRIP-seq:(Medium) rs768298054 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9399625,Human_RBP_ID_18195158 Human_Splice_Rec_713653,Human_Splice_Rec_713673,Human_Splice_Rec_713685,Human_Splice_Rec_713697,Human_Splice_Rec_713709,Human_Splice_Rec_713721 RMVar_hsa_circ_59249,RMVar_hsa_circ_57000,RMVar_hsa_circ_91335,RMVar_hsa_circ_235724,RMVar_hsa_circ_66386,RMVar_hsa_circ_360490 82966 RMVar_ID_82966 Human_SNP_ID_257268709 m1A Human chr5 - 154823483 154823483 154823483 CTTCCTCTATCCCTTCCTCAAATGGTGGAGAGACCCCTGCCGCCGTGAGCTACCCACCTTCCACT CTTCCTCTATCCCTTCCTCAAATGGTGGAGAGCCCCCTGCCGCCGTGAGCTACCCACCTTCCACT T G FAXDC2 Ensembl:ENSG00000170271 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154823442..154823507 26863196 MeRIP-seq:(Medium) rs751260950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9399625,Human_RBP_ID_18195158 Human_Splice_Rec_713653,Human_Splice_Rec_713673,Human_Splice_Rec_713685,Human_Splice_Rec_713697,Human_Splice_Rec_713709,Human_Splice_Rec_713721 RMVar_hsa_circ_59249,RMVar_hsa_circ_57000,RMVar_hsa_circ_91335,RMVar_hsa_circ_235724,RMVar_hsa_circ_66386,RMVar_hsa_circ_360490 82967 RMVar_ID_82967 Human_SNP_ID_257277744 m1A Human chr5 + 154858590 154858590 154858590 GCCGTCCGGTTGTTTGGTGGGAGGCACGTAAGACCGCTCTGGGCACGGGGGCGCTCACCTCACTG GCCGTCCGGTTGTTTGGTGGGAGGCACGTAAGGCCGCTCTGGGCACGGGGGCGCTCACCTCACTG A G CNOT8 Ensembl:ENSG00000155508 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:154858507..154858800 26863196 MeRIP-seq:(Medium) rs1042488729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235726,RMVar_hsa_circ_81803 82968 RMVar_ID_82968 Human_SNP_ID_257277809 m1A Human chr5 + 154858722 154858722 154858722 CCGCCGTCGGGGAGTCAGCCCGCCAGCCCGCCAGCTCGTCAGCCCGCCAGCCAGCGCTTCGCGGG CCGCCGTCGGGGAGTCAGCCCGCCAGCCCGCCTGCTCGTCAGCCCGCCAGCCAGCGCTTCGCGGG A T CNOT8 Ensembl:ENSG00000155508 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154858673..154858773 32194978 MeRIP-seq:(Medium) rs113626307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4819454,Human_RBP_ID_17415421,Human_RBP_ID_18043078,Human_RBP_ID_18425042,Human_RBP_ID_18837027,Human_RBP_ID_22459862 Human_Splice_Rec_713780,Human_Splice_Rec_713781,Human_Splice_Rec_713785,Human_Splice_Rec_713793,Human_Splice_Rec_713805,Human_Splice_Rec_713812,Human_Splice_Rec_713813,Human_Splice_Rec_713820,Human_Splice_Rec_713826,Human_Splice_Rec_713827,Human_Splice_Rec_713834,Human_Splice_Rec_713835,Human_Splice_Rec_713843,Human_Splice_Rec_713855,Human_Splice_Rec_713861,Human_Splice_Rec_713869,Human_Splice_Rec_713881,Human_Splice_Rec_713887,Human_Splice_Rec_713897,Human_Splice_Rec_713909,Human_Splice_Rec_713915,Human_Splice_Rec_713925,Human_Splice_Rec_713929,Human_Splice_Rec_713949 RMVar_hsa_circ_235726,RMVar_hsa_circ_81803 82969 RMVar_ID_82969 Human_SNP_ID_257277947 m1A Human chr5 + 154859208 154859208 154859208 CAAACAAAAACAGAAGAAGAATGGCGTGTCAGAAGGAGGAGGACTGAGTGTGATTTGAAGTGGAA CAAACAAAAACAGAAGAAGAATGGCGTGTCAGGAGGAGGAGGACTGAGTGTGATTTGAAGTGGAA A G CNOT8 Ensembl:ENSG00000155508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154859204..154859273 26863196 MeRIP-seq:(Medium) rs1385914505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7409047,Human_RBP_ID_15360429,Human_RBP_ID_24092402 RMVar_hsa_circ_235726,RMVar_hsa_circ_81803 82970 RMVar_ID_82970 Human_SNP_ID_257278872 m1A Human chr5 - 154863150 154863150 154863150 CATGTAAGTTTACACACACATAAGATGTCAACACAACAAAGACATCAAAATAATATTTTACAATC CATGTAAGTTTACACACACATAAGATGTCAACGCAACAAAGACATCAAAATAATATTTTACAATC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:154863147..154863235 26863410 MeRIP-seq:(Medium) rs1334861193 Functional Loss SNV dbSNP153 33..33 33 - - - 82971 RMVar_ID_82971 Human_SNP_ID_257278902 m1A Human chr5 + 154863300 154863300 154863300 GTTTCTTCAGGATGCCTGCAGCACTTGTGGAGAATAGCCAGGTTATCTGTGAAGTGTGGGCCAGT GTTTCTTCAGGATGCCTGCAGCACTTGTGGAGCATAGCCAGGTTATCTGTGAAGTGTGGGCCAGT A C CNOT8 Ensembl:ENSG00000155508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154863276..154863300 26863196 MeRIP-seq:(Medium) rs1256816468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946626,Human_RBP_ID_1991070,Human_RBP_ID_4819469,Human_RBP_ID_7409072,Human_RBP_ID_8608429,Human_RBP_ID_18837031 Human_Splice_Rec_713782,Human_Splice_Rec_713794,Human_Splice_Rec_713795,Human_Splice_Rec_713806,Human_Splice_Rec_713807,Human_Splice_Rec_713814,Human_Splice_Rec_713815,Human_Splice_Rec_713821,Human_Splice_Rec_713844,Human_Splice_Rec_713845,Human_Splice_Rec_713856,Human_Splice_Rec_713857,Human_Splice_Rec_713870,Human_Splice_Rec_713871,Human_Splice_Rec_713884,Human_Splice_Rec_713885,Human_Splice_Rec_713912,Human_Splice_Rec_713913,Human_Splice_Rec_713916,Human_Splice_Rec_713917,Human_Splice_Rec_713926,Human_Splice_Rec_713927,Human_Splice_Rec_713930,Human_Splice_Rec_713931,Human_Splice_Rec_713940,Human_Splice_Rec_713941,Human_Splice_Rec_713950,Human_Splice_Rec_713951,Human_Splice_Rec_713962,Human_Splice_Rec_713963 Human_miRNA_ID_2723394 RMVar_hsa_circ_235726,RMVar_hsa_circ_81803,RMVar_hsa_circ_303656,RMVar_hsa_circ_337916,RMVar_hsa_circ_361054 82972 RMVar_ID_82972 Human_SNP_ID_257281336 m1A Human chr5 - 154872613 154872613 154872613 CATCCTAAAGAAAGCCATTCCTGTCAGCAGTGAGTCTGAGCCTGCCTGGTGCTGCCTTCCAATCC CATCCTAAAGAAAGCCATTCCTGTCAGCAGTGGGTCTGAGCCTGCCTGGTGCTGCCTTCCAATCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154871847..154872613 32194978 MeRIP-seq:(Medium) rs368235746 Functional Loss SNV dbSNP153 33..33 33 - - - 82973 RMVar_ID_82973 Human_SNP_ID_257282040 m1A Human chr5 - 154875498 154875498 154875498 AAGAAGCATTTTCTCTTGGGGAAGATAAGTACACAGTCAGCACAGTAAGCACCACTCTGGGATCA AAGAAGCATTTTCTCTTGGGGAAGATAAGTACGCAGTCAGCACAGTAAGCACCACTCTGGGATCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154875449..154875650 32194978 MeRIP-seq:(Medium) rs1324447390 Functional Loss SNV dbSNP153 33..33 33 - - - 82974 RMVar_ID_82974 Human_SNP_ID_257286434 m1A Human chr5 + 154892467 154892467 154892467 CTGAGTCATAGCTCCGGACCACCGCCCGAAGGAGCGCCTGCACAGCCTCGTCCCAGGAGGCCATC CTGAGTCATAGCTCCGGACCACCGCCCGAAGGGGCGCCTGCACAGCCTCGTCCCAGGAGGCCATC A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154892421..154892522 32194978 MeRIP-seq:(Medium) rs765893701 Functional Loss SNV dbSNP153 33..33 33 - - - 82975 RMVar_ID_82975 Human_SNP_ID_257293958 m1A Human chr5 + 154920018 154920018 154920018 CTGATGAGTTTGTTGATGTCAAAGGCTTCTCCACTAAGCTTCCAGGGATTATGCTGTAAGACAAT CTGATGAGTTTGTTGATGTCAAAGGCTTCTCCGCTAAGCTTCCAGGGATTATGCTGTAAGACAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154917021..154927432 32194978 MeRIP-seq:(Medium) rs543651409 Functional Loss SNV dbSNP153 33..33 33 - - - 82976 RMVar_ID_82976 Human_SNP_ID_257298863 m1A Human chr5 + 154937972 154937972 154937972 AGTCTCGGGCCCAAGGGTGGTGAGTTACCTCGAAACGGGGGTGTCCCTGGACTCTCGCCTGCGCC AGTCTCGGGCCCAAGGGTGGTGAGTTACCTCGCAACGGGGGTGTCCCTGGACTCTCGCCTGCGCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154935975..154938009 32194978 MeRIP-seq:(Medium) rs1399801803 Functional Loss SNV dbSNP153 33..33 33 - - - 82977 RMVar_ID_82977 Human_SNP_ID_257299759 m1A Human chr5 + 154941131 154941131 154941131 GGAGGGCGAAAGATGGCGGCGGCAGTACTGGGACAGTTGGGTAAGGATTTCTTAGTGGTTAAGCG GGAGGGCGAAAGATGGCGGCGGCAGTACTGGGGCAGTTGGGTAAGGATTTCTTAGTGGTTAAGCG A G MRPL22 Ensembl:ENSG00000082515 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:154941076..154941301;chr5:154941076..154941332 26863196 MeRIP-seq:(Medium) rs1293892096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789157,Human_RBP_ID_5509143 Human_Splice_Rec_714031,Human_Splice_Rec_714043,Human_Splice_Rec_714063 82978 RMVar_ID_82978 Human_SNP_ID_257301875 m1A Human chr5 - 154950758 154950758 154950758 AGACACTTAGGGGACCTTTCTGTAGAGTTTACATATCTTTTGAACCACTTCAGCTCCATTTTGAT AGACACTTAGGGGACCTTTCTGTAGAGTTTACGTATCTTTTGAACCACTTCAGCTCCATTTTGAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154950756..154950950 26863196 MeRIP-seq:(Medium) rs752859522 Functional Loss SNV dbSNP153 33..33 33 - - - 82979 RMVar_ID_82979 Human_SNP_ID_257301876 m1A Human chr5 - 154950758 154950758 154950758 AGACACTTAGGGGACCTTTCTGTAGAGTTTACATATCTTTTGAACCACTTCAGCTCCATTTTGAT AGACACTTAGGGGACCTTTCTGTAGAGTTTACCTATCTTTTGAACCACTTCAGCTCCATTTTGAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:154950756..154950950 26863196 MeRIP-seq:(Medium) rs752859522 Functional Loss SNV dbSNP153 33..33 33 - - - 82980 RMVar_ID_82980 Human_SNP_ID_257301926 m1A Human chr5 - 154950890 154950890 154950890 TCTCCAGGCAGTTGTGGAGGATAAACAATTTTATTCTTCTTCTCCCATTTTCGAGAAATGTCAAG TCTCCAGGCAGTTGTGGAGGATAAACAATTTTCTTCTTCTTCTCCCATTTTCGAGAAATGTCAAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154950801..154950900 32194978 MeRIP-seq:(Medium) rs368650810 Functional Loss SNV dbSNP153 33..33 33 - - - 82981 RMVar_ID_82981 Human_SNP_ID_257303202 m1A Human chr5 - 154956419 154956419 154956419 GTCATTGCAGCTTACCAATTTTGCCAAATACCACATCTTGTCTTTGCTATATTTTATTTGTCTTC GTCATTGCAGCTTACCAATTTTGCCAAATACCGCATCTTGTCTTTGCTATATTTTATTTGTCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:154956351..154956450 26863196 MeRIP-seq:(Medium) rs1195369253 Functional Loss SNV dbSNP153 33..33 33 - - - 82982 RMVar_ID_82982 Human_SNP_ID_257303203 m1A Human chr5 - 154956419 154956419 154956419 GTCATTGCAGCTTACCAATTTTGCCAAATACCACATCTTGTCTTTGCTATATTTTATTTGTCTTC GTCATTGCAGCTTACCAATTTTGCCAAATACCCCATCTTGTCTTTGCTATATTTTATTTGTCTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:154956351..154956450 26863196 MeRIP-seq:(Medium) rs1195369253 Functional Loss SNV dbSNP153 33..33 33 - - - 82983 RMVar_ID_82983 Human_SNP_ID_257316548 m1A Human chr5 + 155013890 155013890 155013890 TCATGAAGGAAGAGGTGAAGGGAATTCCTGTAAGAGTGGCACTGCGTTGTCGCCCTCTGGTCCCC TCATGAAGGAAGAGGTGAAGGGAATTCCTGTACGAGTGGCACTGCGTTGTCGCCCTCTGGTCCCC A C KIF4B Ensembl:ENSG00000226650 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:155013841..155013925 26863196 MeRIP-seq:(Medium) rs1462069098 Functional Loss SNV dbSNP153 33..33 33 - - - 82984 RMVar_ID_82984 Human_SNP_ID_257846877 m1A Human chr5 + 157142786 157142786 157142786 AGCTGCGGGGTCCGGAAGAAAAAAACGCACACAGGCGGCGGCCCCAAACCGTTGCCGCCCACTTA AGCTGCGGGGTCCGGAAGAAAAAAACGCACACCGGCGGCGGCCCCAAACCGTTGCCGCCCACTTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:157142777..157142842 26863196 MeRIP-seq:(Medium) rs1260432212 Functional Loss SNV dbSNP153 33..33 33 - - - 82985 RMVar_ID_82985 Human_SNP_ID_257996170 m1A Human chr5 + 157743829 157743829 157743829 CCGCGCGCCCGCCCAGCCCGCGGCTGGATGTCAGCTCTGACAGCTTCGACCCGCTGCTGGCCCTG CCGCGCGCCCGCCCAGCCCGCGGCTGGATGTCGGCTCTGACAGCTTCGACCCGCTGCTGGCCCTG A G LSM11 Ensembl:ENSG00000155858 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:157743778..157743935 26863196 MeRIP-seq:(Medium) rs761244096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1487182 82986 RMVar_ID_82986 Human_SNP_ID_257996173 m1A Human chr5 - 157743834 157743834 157743834 GCGTACAGGGCCAGCAGCGGGTCGAAGCTGTCAGAGCTGACATCCAGCCGCGGGCTGGGCGGGCG GCGTACAGGGCCAGCAGCGGGTCGAAGCTGTCGGAGCTGACATCCAGCCGCGGGCTGGGCGGGCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr5:157743785..157743874;chr5:157743784..157743880 26863410,26863196 MeRIP-seq:(Medium) rs1213775511 Functional Loss SNV dbSNP153 33..33 33 - - - 82987 RMVar_ID_82987 Human_SNP_ID_257996445 m1A Human chr5 - 157744483 157744483 157744483 GTGACCCTTCCATGGGCCCCGATTACCGCTGAAGACCTTTCCCACGGCTTCTTATGACCACTACA GTGACCCTTCCATGGGCCCCGATTACCGCTGAGGACCTTTCCCACGGCTTCTTATGACCACTACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:157744010..157744649 26863196 MeRIP-seq:(Medium) rs1388670988 Functional Loss SNV dbSNP153 33..33 33 - - - 82988 RMVar_ID_82988 Human_SNP_ID_258006978 m1A Human chr5 - 157786487 157786485 157786488 TAATTCTGCATTAAGCTCACATGAAAATCATGATTCTAGAGTTTGGAATGCAAAATTAATTGTTT TAATTCTGCATTAAGCTCACATGAAAATCAT___TCTAGAGTTTGGAATGCAAAATTAATTGTTT AATC A CLINT1 Ensembl:ENSG00000113282 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:157786438..157786539 32194978 MeRIP-seq:(Medium) rs1279110178 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_636337,Human_RBP_ID_1649035,Human_RBP_ID_7409867,Human_RBP_ID_18355870,Human_RBP_ID_22402787,Human_RBP_ID_24093182,Human_RBP_ID_26523984 Human_miRNA_ID_1274698 82989 RMVar_ID_82989 Human_SNP_ID_258006980 m1A Human chr5 - 157786487 157786487 157786487 TAATTCTGCATTAAGCTCACATGAAAATCATGATTCTAGAGTTTGGAATGCAAAATTAATTGTTT TAATTCTGCATTAAGCTCACATGAAAATCATGGTTCTAGAGTTTGGAATGCAAAATTAATTGTTT T C CLINT1 Ensembl:ENSG00000113282 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:157786438..157786539 32194978 MeRIP-seq:(Medium) rs971093097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_636337,Human_RBP_ID_1649035,Human_RBP_ID_7409867,Human_RBP_ID_18355870,Human_RBP_ID_22402787,Human_RBP_ID_24093182,Human_RBP_ID_26523984 Human_miRNA_ID_1274698 82990 RMVar_ID_82990 Human_SNP_ID_258012351 m1A Human chr5 - 157809592 157809589 157809593 TTTTACCACTTTGTCTCCCGGGTCTCTTAGAAAGAGCCCTAAATTTATGCCACTGGGTTTTTGGT TTTTACCACTTTGTCTCCCGGGTCTCTTAGA____GCCCTAAATTTATGCCACTGGGTTTTTGGT CTCTT C CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:157809590..157809702 26863196 MeRIP-seq:(Medium) rs772150695 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_19126685 RMVar_hsa_circ_59322,RMVar_hsa_circ_267249,RMVar_hsa_circ_56821,RMVar_hsa_circ_235861,RMVar_hsa_circ_265458,RMVar_hsa_circ_371013,RMVar_hsa_circ_372288,RMVar_hsa_circ_235863,RMVar_hsa_circ_123030,RMVar_hsa_circ_235862,RMVar_hsa_circ_346953,RMVar_hsa_circ_235865,RMVar_hsa_circ_353873,RMVar_hsa_circ_357192,RMVar_hsa_circ_306753,RMVar_hsa_circ_353910,RMVar_hsa_circ_354225 82991 RMVar_ID_82991 Human_SNP_ID_258012355 m1A Human chr5 - 157809592 157809592 157809592 TTTTACCACTTTGTCTCCCGGGTCTCTTAGAAAGAGCCCTAAATTTATGCCACTGGGTTTTTGGT TTTTACCACTTTGTCTCCCGGGTCTCTTAGAAGGAGCCCTAAATTTATGCCACTGGGTTTTTGGT T C CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:157809590..157809702 26863196 MeRIP-seq:(Medium) rs748015820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126685 RMVar_hsa_circ_59322,RMVar_hsa_circ_267249,RMVar_hsa_circ_56821,RMVar_hsa_circ_235861,RMVar_hsa_circ_265458,RMVar_hsa_circ_371013,RMVar_hsa_circ_372288,RMVar_hsa_circ_235863,RMVar_hsa_circ_123030,RMVar_hsa_circ_235862,RMVar_hsa_circ_346953,RMVar_hsa_circ_235865,RMVar_hsa_circ_353873,RMVar_hsa_circ_357192,RMVar_hsa_circ_306753,RMVar_hsa_circ_353910,RMVar_hsa_circ_354225 82992 RMVar_ID_82992 Human_SNP_ID_258013223 m1A Human chr5 + 157813226 157813226 157813226 CGAATATTTATACCTTGATCCTTACCATGCTCATCTATGAGGATGGTAAGAGATAAGCAAAACCT CGAATATTTATACCTTGATCCTTACCATGCTCGTCTATGAGGATGGTAAGAGATAAGCAAAACCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:157813186..157814244 32194978 MeRIP-seq:(Medium) rs756448809 Functional Loss SNV dbSNP153 33..33 33 - - - 82993 RMVar_ID_82993 Human_SNP_ID_258358666 m1A Human chr5 - 159203627 159203627 159203627 TAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAACTGGA TAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAGAAAAACAACATGGCTGCAAAGGAGAAACTGGA T C RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:159203576..159207530 26863196 MeRIP-seq:(Medium) rs550823653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25939067 Human_Splice_Rec_715596,Human_Splice_Rec_715616,Human_Splice_Rec_715636,Human_Splice_Rec_715658,Human_Splice_Rec_715700,Human_Splice_Rec_715720,Human_Splice_Rec_715750 RMVar_hsa_circ_235887,RMVar_hsa_circ_128083,RMVar_hsa_circ_55911,RMVar_hsa_circ_235888,RMVar_hsa_circ_281357,RMVar_hsa_circ_337771,RMVar_hsa_circ_235889,RMVar_hsa_circ_347356 82994 RMVar_ID_82994 Human_SNP_ID_258359812 m1A Human chr5 - 159208046 159208046 159208046 AGATTAGTGGATGGCCTTGCGTCGCAGTCTGCAGTAAAGAGGAAACTAGTCTGAAAGGGAAGGAG AGATTAGTGGATGGCCTTGCGTCGCAGTCTGCGGTAAAGAGGAAACTAGTCTGAAAGGGAAGGAG T C RNF145 Ensembl:ENSG00000145860 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:159208043..159208109 26863196 MeRIP-seq:(Medium) rs1406273724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5214593 82995 RMVar_ID_82995 Human_SNP_ID_258360255 m1A Human chr5 + 159209412 159209412 159209412 GCCTCGGATGTTGCTTCTGGGGAGGCGGAGGCAGCGGCAGCGGCAGCGGCCCGGCCCGTACGGTC GCCTCGGATGTTGCTTCTGGGGAGGCGGAGGCGGCGGCAGCGGCAGCGGCCCGGCCCGTACGGTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:159209376..159209528 26863196 MeRIP-seq:(Medium) rs766213455 Functional Loss SNV dbSNP153 33..33 33 - - - 82996 RMVar_ID_82996 Human_SNP_ID_258550523 m1A Human chr5 - 160009193 160009193 160009193 GCCAACACGCTTAGACCCACGGGGTTACTCACAACCTCACAGCTTCTCCGGTCTCCACCTTCTTA GCCAACACGCTTAGACCCACGGGGTTACTCACTACCTCACAGCTTCTCCGGTCTCCACCTTCTTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:160009182..160009268 26863196 MeRIP-seq:(Medium) rs978555100 Functional Loss SNV dbSNP153 33..33 33 - - - 82997 RMVar_ID_82997 Human_SNP_ID_258550944 m1A Human chr5 + 160010641 160010641 160010641 GTGTGCTGGCCCTCCAGTTCCTGATCCCAAAAATCAGCATTCCCAGAGTAAGCTGCTCAGGGATG GTGTGCTGGCCCTCCAGTTCCTGATCCCAAAAGTCAGCATTCCCAGAGTAAGCTGCTCAGGGATG A G TTC1 Ensembl:ENSG00000113312 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:160010501..160010667 32194978 MeRIP-seq:(Medium) rs766245498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18837394 Human_miRNA_ID_2423705,Human_miRNA_ID_2433364,Human_miRNA_ID_2783625 RMVar_hsa_circ_105992,RMVar_hsa_circ_235898,RMVar_hsa_circ_104720,RMVar_hsa_circ_300823,RMVar_hsa_circ_343924,RMVar_hsa_circ_351422,RMVar_hsa_circ_309458,RMVar_hsa_circ_282804,RMVar_hsa_circ_235900,RMVar_hsa_circ_235902,RMVar_hsa_circ_235903,RMVar_hsa_circ_235901,RMVar_hsa_circ_235899 82998 RMVar_ID_82998 Human_SNP_ID_258564110 m1A Human chr5 - 160065391 160065387 160065391 GTCTCCCAACCAACAGGTTTGTTTGGTTCAGGAGAGGCTTTTGCTGGGCTGTGTGTGTGTATGAT GTCTCCCAACCAACAGGTTTGTTTGGTTCAGG____GCTTTTGCTGGGCTGTGTGTGTGTATGAT CCTCT C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:160065343..160065444 32194978 MeRIP-seq:(Medium) rs1480015063 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_11721,RMVar_hsa_circ_43960,RMVar_hsa_circ_235909 82999 RMVar_ID_82999 Human_SNP_ID_258570958 m1A Human chr5 - 160093654 160093654 160093654 TGTGATAAATGTAAAAACAGTGTTGTTGCTGAAAAAAAGGAAATTAGAAAAGGTAGTAGTGCAAC TGTGATAAATGTAAAAACAGTGTTGTTGCTGAGAAAAAGGAAATTAGAAAAGGTAGTAGTGCAAC T C PWWP2A Ensembl:ENSG00000170234 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs56251777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24093892 Human_miRNA_ID_2911592 RMVar_hsa_circ_235911,RMVar_hsa_circ_235912,RMVar_hsa_circ_235914,RMVar_hsa_circ_309048,RMVar_hsa_circ_235915,RMVar_hsa_circ_235918,RMVar_hsa_circ_235917,RMVar_hsa_circ_284059,RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_265474,RMVar_hsa_circ_289857 83000 RMVar_ID_83000 Human_SNP_ID_258577769 m1A Human chr5 - 160118924 160118924 160118924 CCGCCGGCGGGCGGGGACTCCACGGTGTCGCAACTGATCCCGGGCTCGGAGGTGCGGGTCACGCT CCGCCGGCGGGCGGGGACTCCACGGTGTCGCATCTGATCCCGGGCTCGGAGGTGCGGGTCACGCT T A PWWP2A Ensembl:ENSG00000170234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160118875..160119469 26863196 MeRIP-seq:(Medium) rs760340162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4820438,Human_RBP_ID_5213540,Human_RBP_ID_23050181 83001 RMVar_ID_83001 Human_SNP_ID_258577770 m1A Human chr5 - 160118924 160118924 160118924 CCGCCGGCGGGCGGGGACTCCACGGTGTCGCAACTGATCCCGGGCTCGGAGGTGCGGGTCACGCT CCGCCGGCGGGCGGGGACTCCACGGTGTCGCAGCTGATCCCGGGCTCGGAGGTGCGGGTCACGCT T C PWWP2A Ensembl:ENSG00000170234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160118875..160119469 26863196 MeRIP-seq:(Medium) rs760340162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4820438,Human_RBP_ID_5213540,Human_RBP_ID_23050181 83002 RMVar_ID_83002 Human_SNP_ID_258615539 m1A Human chr5 - 160259594 160259594 160259594 CTGCCTGCCCACGCCTGCCCACTTCCTGGACTACTACCTCTTGGCCTCCGTCAGCCAGAAGGACC CTGCCTGCCCACGCCTGCCCACTTCCTGGACTGCTACCTCTTGGCCTCCGTCAGCCAGAAGGACC T C CCNJL Ensembl:ENSG00000135083 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:160259544..160259673 26863196 MeRIP-seq:(Medium) rs759291791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27513458 Human_miRNA_ID_24515,Human_miRNA_ID_795246,Human_miRNA_ID_1307055,Human_miRNA_ID_1913752,Human_miRNA_ID_1916204,Human_miRNA_ID_1918652,Human_miRNA_ID_1921108,Human_miRNA_ID_1923566,Human_miRNA_ID_1926017,Human_miRNA_ID_1928467,Human_miRNA_ID_1930919,Human_miRNA_ID_2168015,Human_miRNA_ID_2169540,Human_miRNA_ID_2628750,Human_miRNA_ID_2641859,Human_miRNA_ID_3124601 RMVar_hsa_circ_94240,RMVar_hsa_circ_235920 83003 RMVar_ID_83003 Human_SNP_ID_258629818 m1A Human chr5 - 160312448 160312448 160312448 CGGGAGTGCGGAGCGCCTCGGACGAGGGTCCAACCGCCGGCAGGCACCAGAGGGCACGGCTGGCT CGGGAGTGCGGAGCGCCTCGGACGAGGGTCCAGCCGCCGGCAGGCACCAGAGGGCACGGCTGGCT T C CCNJL Ensembl:ENSG00000135083 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:160311837..160312570 26863196 MeRIP-seq:(Medium) rs1364033729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845470 Human_Splice_Rec_716057,Human_Splice_Rec_716069,Human_Splice_Rec_716095,Human_Splice_Rec_716123,Human_Splice_Rec_716137,Human_Splice_Rec_716149,Human_Splice_Rec_716159 RMVar_hsa_circ_94240,RMVar_hsa_circ_235920 83004 RMVar_ID_83004 Human_SNP_ID_258629821 m1A Human chr5 + 160312452 160312452 160312452 AGCCGTGCCCTCTGGTGCCTGCCGGCGGTTGGACCCTCGTCCGAGGCGCTCCGCACTCCCGACGG AGCCGTGCCCTCTGGTGCCTGCCGGCGGTTGGCCCCTCGTCCGAGGCGCTCCGCACTCCCGACGG A C RF00017-1033,RF00017-4513 RNACentral:URS0000984FD7,RNACentral:URS000090EECB SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:160312316..160312555 26863196 MeRIP-seq:(Medium) rs1405577048 Functional Loss SNV dbSNP153 33..33 33 - - - 83005 RMVar_ID_83005 Human_SNP_ID_258629826 m1A Human chr5 - 160312459 160312459 160312459 GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGACGAGGGTCCAACCGCCGGCAGGCACCAGAGGG GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGTCGAGGGTCCAACCGCCGGCAGGCACCAGAGGG T A CCNJL Ensembl:ENSG00000135083 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160312409..160312566 26863196 MeRIP-seq:(Medium) rs912534625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845470 Human_Splice_Rec_716057,Human_Splice_Rec_716069,Human_Splice_Rec_716095,Human_Splice_Rec_716123,Human_Splice_Rec_716137,Human_Splice_Rec_716149,Human_Splice_Rec_716159 RMVar_hsa_circ_94240,RMVar_hsa_circ_235920 83006 RMVar_ID_83006 Human_SNP_ID_258629827 m1A Human chr5 - 160312459 160312459 160312459 GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGACGAGGGTCCAACCGCCGGCAGGCACCAGAGGG GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGGCGAGGGTCCAACCGCCGGCAGGCACCAGAGGG T C CCNJL Ensembl:ENSG00000135083 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160312409..160312566 26863196 MeRIP-seq:(Medium) rs912534625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845470 Human_Splice_Rec_716057,Human_Splice_Rec_716069,Human_Splice_Rec_716095,Human_Splice_Rec_716123,Human_Splice_Rec_716137,Human_Splice_Rec_716149,Human_Splice_Rec_716159 RMVar_hsa_circ_94240,RMVar_hsa_circ_235920 83007 RMVar_ID_83007 Human_SNP_ID_258629828 m1A Human chr5 - 160312459 160312459 160312459 GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGACGAGGGTCCAACCGCCGGCAGGCACCAGAGGG GAGGCGGCCGTCGGGAGTGCGGAGCGCCTCGGCCGAGGGTCCAACCGCCGGCAGGCACCAGAGGG T G CCNJL Ensembl:ENSG00000135083 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160312409..160312566 26863196 MeRIP-seq:(Medium) rs912534625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845470 Human_Splice_Rec_716057,Human_Splice_Rec_716069,Human_Splice_Rec_716095,Human_Splice_Rec_716123,Human_Splice_Rec_716137,Human_Splice_Rec_716149,Human_Splice_Rec_716159 RMVar_hsa_circ_94240,RMVar_hsa_circ_235920 83008 RMVar_ID_83008 Human_SNP_ID_258652007 m1A Human chr5 + 160400010 160400010 160400010 TCTGCGGTGCGCCTGGAGAGAGAAGCATCCGCAACAACCTCCGCCTCAGCCAGGCCCGGGTTCCA TCTGCGGTGCGCCTGGAGAGAGAAGCATCCGCGACAACCTCCGCCTCAGCCAGGCCCGGGTTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:160399959..160400031 26863196 MeRIP-seq:(Medium) rs1232855921 Functional Loss SNV dbSNP153 33..33 33 - - - 83009 RMVar_ID_83009 Human_SNP_ID_258653185 m1A Human chr5 - 160404546 160404546 160404546 GCATTTCAATCCTCCCTTTCAGCTGCATCAAGAAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA GCATTTCAATCCTCCCTTTCAGCTGCATCAAGGAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA T C SLU7 Ensembl:ENSG00000164609 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:160404401..160404575 26863196 MeRIP-seq:(Medium) rs776637012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76531,Human_RBP_ID_214286,Human_RBP_ID_1660402,Human_RBP_ID_9349742,Human_RBP_ID_24548066,Human_RBP_ID_26351699,Human_RBP_ID_27826074 Human_Splice_Rec_716212 RMVar_hsa_circ_62418,RMVar_hsa_circ_124361,RMVar_hsa_circ_235923 83010 RMVar_ID_83010 Human_SNP_ID_258656026 m1A Human chr5 - 160415294 160415294 160415294 TCACTTCTTTTCCTAGAGGAGGCCAGATAACCATGTCAGCCACAGTTGTAGATGCAGTTAATGCT TCACTTCTTTTCCTAGAGGAGGCCAGATAACCGTGTCAGCCACAGTTGTAGATGCAGTTAATGCT T C SLU7 Ensembl:ENSG00000164609 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:160415213..160415325 26863410 MeRIP-seq:(Medium) rs937385162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1649310,Human_RBP_ID_5151359,Human_RBP_ID_8236998,Human_RBP_ID_26351706,Human_RBP_ID_27826084 Human_Splice_Rec_716186,Human_Splice_Rec_716228,Human_Splice_Rec_716236,Human_Splice_Rec_716244,Human_Splice_Rec_716252,Human_Splice_Rec_716256 83011 RMVar_ID_83011 Human_SNP_ID_258656029 m1A Human chr5 - 160415300 160415300 160415300 TAAGTTTCACTTCTTTTCCTAGAGGAGGCCAGATAACCATGTCAGCCACAGTTGTAGATGCAGTT TAAGTTTCACTTCTTTTCCTAGAGGAGGCCAGGTAACCATGTCAGCCACAGTTGTAGATGCAGTT T C SLU7 Ensembl:ENSG00000164609 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA heat shock 4h chr5:160415126..160415325 31548705,26863196 m1A-IP-seq:(High) rs571231440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5151359,Human_RBP_ID_26351706,Human_RBP_ID_27826084 Human_Splice_Rec_716186,Human_Splice_Rec_716228,Human_Splice_Rec_716236,Human_Splice_Rec_716244,Human_Splice_Rec_716252,Human_Splice_Rec_716256 83012 RMVar_ID_83012 Human_SNP_ID_258656936 m1A Human chr5 - 160418931 160418931 160418931 GTCGAAGGCTCCTAATTATTGGATATATCTTCACGGGGGTGATGAGCCCTCAGGTGTTGAGGGAG GTCGAAGGCTCCTAATTATTGGATATATCTTCGCGGGGGTGATGAGCCCTCAGGTGTTGAGGGAG T C SLU7 Ensembl:ENSG00000164609 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:160418926..160419075 26863196 MeRIP-seq:(Medium) rs1474330238 Functional Loss SNV dbSNP153 33..33 33 - - - 83013 RMVar_ID_83013 Human_SNP_ID_258658006 m1A Human chr5 + 160422743 160422743 160422743 ATCAAAGCCTTAGATGGGAGATCTCAAGTTTCAACACCACGTTTTGGCAAAACGTTCGATGCCCC ATCAAAGCCTTAGATGGGAGATCTCAAGTTTCGACACCACGTTTTGGCAAAACGTTCGATGCCCC A G PTTG1 Ensembl:ENSG00000164611 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:160422701..160422750 26863196 MeRIP-seq:(Medium) rs781564469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76534,Human_RBP_ID_636613,Human_RBP_ID_946566,Human_RBP_ID_1320439,Human_RBP_ID_1649319,Human_RBP_ID_1991503,Human_RBP_ID_3764045,Human_RBP_ID_7411648,Human_RBP_ID_18043622,Human_RBP_ID_18448446,Human_RBP_ID_18837489,Human_RBP_ID_24094010,Human_RBP_ID_26827606,Human_RBP_ID_27077374 Human_Splice_Rec_716262,Human_Splice_Rec_716266,Human_Splice_Rec_716280,Human_Splice_Rec_716286,Human_Splice_Rec_716294,Human_Splice_Rec_716304 Human_miRNA_ID_2976660 RMVar_hsa_circ_235924,RMVar_hsa_circ_102555,RMVar_hsa_circ_61673,RMVar_hsa_circ_235925,RMVar_hsa_circ_125020,RMVar_hsa_circ_361916,RMVar_hsa_circ_92641,RMVar_hsa_circ_102192,RMVar_hsa_circ_362369,RMVar_hsa_circ_235926,RMVar_hsa_circ_235927 83014 RMVar_ID_83014 Human_SNP_ID_258659149 m1A Human chr5 + 160427721 160427721 160427721 ACAAAAACGCTTTCTCTCTGTAACAGACTTTGAGAGTTTTGACCTGCCTGAAGAGCACCAGATTG ACAAAAACGCTTTCTCTCTGTAACAGACTTTGGGAGTTTTGACCTGCCTGAAGAGCACCAGATTG A G PTTG1 Ensembl:ENSG00000164611 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1370620903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1649327,Human_RBP_ID_1991508,Human_RBP_ID_5121580,Human_RBP_ID_8608971,Human_RBP_ID_9398636,Human_RBP_ID_15367618,Human_RBP_ID_22459024,Human_RBP_ID_24094029,Human_RBP_ID_27333764 Human_Splice_Rec_716270,Human_Splice_Rec_716290,Human_Splice_Rec_716298,Human_Splice_Rec_716308 Human_miRNA_ID_2031866,Human_miRNA_ID_2886807 RMVar_hsa_circ_86650,RMVar_hsa_circ_235924,RMVar_hsa_circ_102555,RMVar_hsa_circ_61673,RMVar_hsa_circ_235925,RMVar_hsa_circ_125020,RMVar_hsa_circ_92641,RMVar_hsa_circ_102192,RMVar_hsa_circ_235926,RMVar_hsa_circ_235927,RMVar_hsa_circ_235928 83015 RMVar_ID_83015 Human_SNP_ID_258659391 m1A Human chr5 - 160428607 160428607 160428607 CAGGGTCGACAGAATGCTTGAAGGAGACTGCAACAGATCTAGAAAACAGGAATCTCTTATTAAAA CAGGGTCGACAGAATGCTTGAAGGAGACTGCAGCAGATCTAGAAAACAGGAATCTCTTATTAAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:160427701..160428675 32194978 MeRIP-seq:(Medium) rs1561573497 Functional Loss SNV dbSNP153 33..33 33 - - - 83016 RMVar_ID_83016 Human_SNP_ID_259435275 m1A Human chr5 + 163437659 163437659 163437659 CGAGTTGTCTCGGCGGCGCTGCCGAGGCCTCCACCCAGGACAGTCCCCCTCCCCGGGCCTCTCTC CGAGTTGTCTCGGCGGCGCTGCCGAGGCCTCCGCCCAGGACAGTCCCCCTCCCCGGGCCTCTCTC A G CCNG1 Ensembl:ENSG00000113328 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:163437608..163437740 26863196 MeRIP-seq:(Medium) rs1159333638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_636641,Human_RBP_ID_787622,Human_RBP_ID_4820630,Human_RBP_ID_5427052,Human_RBP_ID_5449545,Human_RBP_ID_5476424,Human_RBP_ID_5509191,Human_RBP_ID_9173495,Human_RBP_ID_9335443,Human_RBP_ID_25876147,Human_RBP_ID_27077396 Human_Splice_Rec_717537 Human_miRNA_ID_2039215,Human_miRNA_ID_3018195 RMVar_hsa_circ_122441,RMVar_hsa_circ_235941 83017 RMVar_ID_83017 Human_SNP_ID_259436887 m1A Human chr5 + 163443675 163443673 163443676 TGGATTTTGTTTGTTTTCTTTATTTAAATAGGATTATTACAGCACCAAAAAACTTCTCTGAAGCC TGGATTTTGTTTGTTTTCTTTATTTAAATAG___TATTACAGCACCAAAAAACTTCTCTGAAGCC GGAT G CCNG1 Ensembl:ENSG00000113328 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1471707461 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1320451,Human_RBP_ID_1991531,Human_RBP_ID_3764092,Human_RBP_ID_7411948,Human_RBP_ID_8267442,Human_RBP_ID_8609031,Human_RBP_ID_17299189,Human_RBP_ID_17412701,Human_RBP_ID_17528730,Human_RBP_ID_18043702,Human_RBP_ID_18356036,Human_RBP_ID_18537853,Human_RBP_ID_27737729 Human_Splice_Rec_717522,Human_Splice_Rec_717536,Human_Splice_Rec_717552,Human_Splice_Rec_717568,Human_Splice_Rec_717578,Human_Splice_Rec_717586 RMVar_hsa_circ_117727,RMVar_hsa_circ_122441,RMVar_hsa_circ_235941,RMVar_hsa_circ_82115,RMVar_hsa_circ_97361,RMVar_hsa_circ_235942,RMVar_hsa_circ_235943,RMVar_hsa_circ_235944,RMVar_hsa_circ_95296,RMVar_hsa_circ_235945,RMVar_hsa_circ_235946,RMVar_hsa_circ_235947 83018 RMVar_ID_83018 Human_SNP_ID_259440945 m1A Human chr5 + 163459977 163459977 163459977 GCGGCACCTGAACTTCAATGAACACCTCCTCCAAGGTCTGGTACCACTGGCCCCACGGGGTCCCG GCGGCACCTGAACTTCAATGAACACCTCCTCCGAGGTCTGGTACCACTGGCCCCACGGGGTCCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:163459926..163460095 26863196 MeRIP-seq:(Medium) rs753333910 Functional Loss SNV dbSNP153 33..33 33 - - - 83019 RMVar_ID_83019 Human_SNP_ID_259440946 m1A Human chr5 + 163459977 163459977 163459977 GCGGCACCTGAACTTCAATGAACACCTCCTCCAAGGTCTGGTACCACTGGCCCCACGGGGTCCCG GCGGCACCTGAACTTCAATGAACACCTCCTCCTAGGTCTGGTACCACTGGCCCCACGGGGTCCCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:163459926..163460095 26863196 MeRIP-seq:(Medium) rs753333910 Functional Loss SNV dbSNP153 33..33 33 - - - 83020 RMVar_ID_83020 Human_SNP_ID_259440953 m1A Human chr5 + 163459999 163459999 163459999 CACCTCCTCCAAGGTCTGGTACCACTGGCCCCACGGGGTCCCGCACGGTACCACCCCACTCCGCT CACCTCCTCCAAGGTCTGGTACCACTGGCCCCTCGGGGTCCCGCACGGTACCACCCCACTCCGCT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr5:163459951..163460125;chr5:163459901..163460086 26863196,26863410 MeRIP-seq:(Medium) rs1169884914 Functional Loss SNV dbSNP153 33..33 33 - - - 83021 RMVar_ID_83021 Human_SNP_ID_259440964 m1A Human chr5 + 163460019 163460019 163460019 ACCACTGGCCCCACGGGGTCCCGCACGGTACCACCCCACTCCGCTCCTCAAACGGGGCCGACATA ACCACTGGCCCCACGGGGTCCCGCACGGTACCGCCCCACTCCGCTCCTCAAACGGGGCCGACATA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:163459909..163460150;chr5:163459901..163460150 26863196 MeRIP-seq:(Medium) rs1326916706 Functional Loss SNV dbSNP153 33..33 33 - - - 83022 RMVar_ID_83022 Human_SNP_ID_259451605 m1A Human chr5 - 163503360 163503360 163503360 CTCCAGAATTATTTCAGGAGAGCAGATACGGGATGGGTCTTAGCCTCTGCCTTCTCTTGCTGGGT CTCCAGAATTATTTCAGGAGAGCAGATACGGGGTGGGTCTTAGCCTCTGCCTTCTCTTGCTGGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:163503311..163503411 26863196 MeRIP-seq:(Medium) rs768117195 Functional Loss SNV dbSNP153 33..33 33 - - - 83023 RMVar_ID_83023 Human_SNP_ID_259452211 m1A Human chr5 - 163505660 163505660 163505660 CACCATGCCCGCCGTCTTCACGCCGCAGCCTCAGCGGCCGCCACCTCCTCCAACCCAGGATCGAC CACCATGCCCGCCGTCTTCACGCCGCAGCCTCGGCGGCCGCCACCTCCTCCAACCCAGGATCGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:163505601..163512132;chr5:163505601..163512150;chr5:163505601..163512100 26863196 MeRIP-seq:(Medium) rs777248803 Functional Loss SNV dbSNP153 33..33 33 - - - 83024 RMVar_ID_83024 Human_SNP_ID_259454565 m1A Human chr5 + 163513993 163513993 163513993 GATGGAGAAAAGGCTGTCCTGGAGAACAATCTAGGTAAGACCTAATCTATTTAGCCCCTGATTGT GATGGAGAAAAGGCTGTCCTGGAGAACAATCTGGGTAAGACCTAATCTATTTAGCCCCTGATTGT A G MAT2B Ensembl:ENSG00000038274 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11546512 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_717787,Human_Splice_Rec_717799,Human_Splice_Rec_717809,Human_Splice_Rec_717817,Human_Splice_Rec_717827,Human_Splice_Rec_717837 RMVar_hsa_circ_235952,RMVar_hsa_circ_286323,RMVar_hsa_circ_297000,RMVar_hsa_circ_360314,RMVar_hsa_circ_235953,RMVar_hsa_circ_59204,RMVar_hsa_circ_280753,RMVar_hsa_circ_349278,RMVar_hsa_circ_235954 83025 RMVar_ID_83025 Human_SNP_ID_549771011 m1A Human chr14 + 30559238 30559238 30559238 GCCCCGACGTACAGCGGGCCGGGAAAAGTGGCACTGAGGCTCTGGAACTTCTGCCCAGCTCTCCT GCCCCGACGTACAGCGGGCCGGGAAAAGTGGCCCTGAGGCTCTGGAACTTCTGCCCAGCTCTCCT A C G2E3 Ensembl:ENSG00000092140 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:30559188..30559384;chr14:30559188..30559324 26863196 MeRIP-seq:(Medium) rs1415594559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758095,Human_RBP_ID_1492385,Human_RBP_ID_1817401,Human_RBP_ID_4291286,Human_RBP_ID_6337228,Human_RBP_ID_9282150,Human_RBP_ID_12307258,Human_RBP_ID_18417924,Human_RBP_ID_18435762,Human_RBP_ID_18648991,Human_RBP_ID_22044487,Human_RBP_ID_22495359,Human_RBP_ID_22926451 Human_Splice_Rec_1503555,Human_Splice_Rec_1503565,Human_Splice_Rec_1503581,Human_Splice_Rec_1503607,Human_Splice_Rec_1503635,Human_Splice_Rec_1503643 83026 RMVar_ID_83026 Human_SNP_ID_549771013 m1A Human chr14 - 30559240 30559240 30559240 CAAGGAGAGCTGGGCAGAAGTTCCAGAGCCTCAGTGCCACTTTTCCCGGCCCGCTGTACGTCGGG CAAGGAGAGCTGGGCAGAAGTTCCAGAGCCTCGGTGCCACTTTTCCCGGCCCGCTGTACGTCGGG T C G2E3-AS1 Ensembl:ENSG00000257636 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:30559189..30559294 26863196 MeRIP-seq:(Medium) rs925581378 Functional Loss SNV dbSNP153 33..33 33 - - - 83027 RMVar_ID_83027 Human_SNP_ID_549845487 m1A Human chr14 - 30874642 30874642 30874642 AGACAGGCTGGGAGCGACAAAGAAACAGGGACAGAGGCGTCAGGGATCCCTCGCACCCGCGCCCG AGACAGGCTGGGAGCGACAAAGAAACAGGGACGGAGGCGTCAGGGATCCCTCGCACCCGCGCCCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:30874526..30874712 26863410 MeRIP-seq:(Medium) rs1293773392 Functional Loss SNV dbSNP153 33..33 33 - - - 83028 RMVar_ID_83028 Human_SNP_ID_549845537 m1A Human chr14 - 30874815 30874815 30874815 CCGCACCCTTCGGATCCCCGGGCGCGGCGCAGAGGAGAGAGGACACAGACGACCCGCTGCTCCAG CCGCACCCTTCGGATCCCCGGGCGCGGCGCAGTGGAGAGAGGACACAGACGACCCGCTGCTCCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:30874811..30875010 26863410 MeRIP-seq:(Medium) rs1348693080 Functional Loss SNV dbSNP153 33..33 33 - - - 83029 RMVar_ID_83029 Human_SNP_ID_549846352 m1A Human chr14 - 30877675 30877675 30877675 ATGCTCGATACAGAAGCATATACTATGTTCCCATACACAGAGAATTCCTCAAGAGGGCAGCCCCC ATGCTCGATACAGAAGCATATACTATGTTCCCGTACACAGAGAATTCCTCAAGAGGGCAGCCCCC T C AL049830.3 Ensembl:ENSG00000258525 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:30877626..30877725 32194978 MeRIP-seq:(Medium) rs1566406820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6338746 83030 RMVar_ID_83030 Human_SNP_ID_549885811 m1A Human chr14 - 31025877 31025877 31025877 CTGCAGGTACCTCGTTGGGGTCGGTGTGCGGGAGCTGCGGCGGCTGGGTTCCCGGCCGGGGGGTG CTGCAGGTACCTCGTTGGGGTCGGTGTGCGGGTGCTGCGGCGGCTGGGTTCCCGGCCGGGGGGTG T A STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:31025875..31026382 26863196 MeRIP-seq:(Medium) rs772195310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087607,Human_RBP_ID_5315646,Human_RBP_ID_26778062 83031 RMVar_ID_83031 Human_SNP_ID_549885812 m1A Human chr14 - 31025877 31025877 31025877 CTGCAGGTACCTCGTTGGGGTCGGTGTGCGGGAGCTGCGGCGGCTGGGTTCCCGGCCGGGGGGTG CTGCAGGTACCTCGTTGGGGTCGGTGTGCGGGCGCTGCGGCGGCTGGGTTCCCGGCCGGGGGGTG T G STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:31025875..31026382 26863196 MeRIP-seq:(Medium) rs772195310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087607,Human_RBP_ID_5315646,Human_RBP_ID_26778062 83032 RMVar_ID_83032 Human_SNP_ID_549885847 m1A Human chr14 - 31025941 31025941 31025941 CATCCAGCACGAGTGGGCTCGGTTCGAGATGGAGCGGGCGCACTGGGAGGTGGAACGGGCCGAAC CATCCAGCACGAGTGGGCTCGGTTCGAGATGGGGCGGGCGCACTGGGAGGTGGAACGGGCCGAAC T C STRN3 Ensembl:ENSG00000196792 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:31025920..31026379 26863196 MeRIP-seq:(Medium) rs867807044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4312092,Human_RBP_ID_5315646,Human_RBP_ID_6339794,Human_RBP_ID_12313725,Human_RBP_ID_22578207 Human_Splice_Rec_1504491,Human_Splice_Rec_1504519,Human_Splice_Rec_1504551 83033 RMVar_ID_83033 Human_SNP_ID_549885872 m1A Human chr14 + 31025994 31025994 31025994 TCGTGCTGGATGTAGTGCAGTATCCCCGGGATAGTGTACTGCTGCGGCCGGGACAGCTCGGGGCC TCGTGCTGGATGTAGTGCAGTATCCCCGGGATGGTGTACTGCTGCGGCCGGGACAGCTCGGGGCC A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:31025972..31026378 26863196 MeRIP-seq:(Medium) rs1399834604 Functional Loss SNV dbSNP153 33..33 33 - - - 83034 RMVar_ID_83034 Human_SNP_ID_549896287 m1A Human chr14 + 31066068 31066068 31066068 TTATTTACTGTTTATCTATAAAAACATTTAATATAATTATTTGAGAAATTTGATCTTGCCTTTCT TTATTTACTGTTTATCTATAAAAACATTTAATGTAATTATTTGAGAAATTTGATCTTGCCTTTCT A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:31066065..31066136 26863196 MeRIP-seq:(Medium) rs1235139380 Functional Loss SNV dbSNP153 33..33 33 - - - 83035 RMVar_ID_83035 Human_SNP_ID_549933090 m1A Human chr14 + 31207603 31207603 31207603 GAAGCGAGAGGTTCTCGCGTGCGGCAGCAGCCAGCGGACGTCCAGTCCCCAGCACGCGGCTCCTC GAAGCGAGAGGTTCTCGCGTGCGGCAGCAGCCGGCGGACGTCCAGTCCCCAGCACGCGGCTCCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:31207554..31207655 26863196 MeRIP-seq:(Medium) rs1198725095 Functional Loss SNV dbSNP153 33..33 33 - - - 83036 RMVar_ID_83036 Human_SNP_ID_549957254 m1A Human chr14 + 31300177 31300174 31300178 TTTCCCTACTAATTGCCATTCACGACTCTTACACACTCTTCCATCCAAATCCACACCCCCTCATT TTTCCCTACTAATTGCCATTCACGACTCTT____ACTCTTCCATCCAAATCCACACCCCCTCATT TACAC T AL136418.3 Ensembl:ENSG00000257831 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:31300126..31300238 26863196 MeRIP-seq:(Medium) rs1212949808 Functional Loss DEL dbSNP153 31..34 33 - - - 83037 RMVar_ID_83037 Human_SNP_ID_549957255 m1A Human chr14 + 31300177 31300174 31300178 TTTCCCTACTAATTGCCATTCACGACTCTTACACACTCTTCCATCCAAATCCACACCCCCTCATT TTTCCCTACTAATTGCCATTCACGACTCTTAC__ACTCTTCCATCCAAATCCACACCCCCTCATT TACAC TAC AL136418.3 Ensembl:ENSG00000257831 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:31300126..31300238 26863196 MeRIP-seq:(Medium) rs1212949808 Functional Loss DEL dbSNP153 33..34 33 - - - 83038 RMVar_ID_83038 Human_SNP_ID_549987240 m1A Human chr14 - 31420498 31420498 31420498 GAGCAGCCGGTAACGTTGCTGGACCGGGACGCACGCTCAGCTGAGGAGGACCCCCAAAGGCAGGC GAGCAGCCGGTAACGTTGCTGGACCGGGACGCCCGCTCAGCTGAGGAGGACCCCCAAAGGCAGGC T G AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:31402960..31420535 26863196 MeRIP-seq:(Medium) rs1033891615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308256,Human_RBP_ID_18649427 RMVar_hsa_circ_99941,RMVar_hsa_circ_165686 83039 RMVar_ID_83039 Human_SNP_ID_549987253 m1A Human chr14 + 31420511 31420511 31420511 GGTCCTCCTCAGCTGAGCGTGCGTCCCGGTCCAGCAACGTTACCGGCTGCTCTGCTAACCCTAGC GGTCCTCCTCAGCTGAGCGTGCGTCCCGGTCCGGCAACGTTACCGGCTGCTCTGCTAACCCTAGC A G AL139353.2 Ensembl:ENSG00000250365 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr14:31420335..31420535;chr14:31420402..31420550 26863196 MeRIP-seq:(Medium) rs117316022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1505419 83040 RMVar_ID_83040 Human_SNP_ID_549987254 m1A Human chr14 + 31420511 31420511 31420511 GGTCCTCCTCAGCTGAGCGTGCGTCCCGGTCCAGCAACGTTACCGGCTGCTCTGCTAACCCTAGC GGTCCTCCTCAGCTGAGCGTGCGTCCCGGTCCTGCAACGTTACCGGCTGCTCTGCTAACCCTAGC A T AL139353.2 Ensembl:ENSG00000250365 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr14:31420335..31420535;chr14:31420402..31420550 26863196 MeRIP-seq:(Medium) rs117316022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1505419 83041 RMVar_ID_83041 Human_SNP_ID_549995904 m1A Human chr14 + 31457392 31457377 31457393 CCCGGGCCTGAGGAATCCGGCTACCCTCAGCCATGGCTTAAGCCAGCGCCGCGGCCGGACAGTTA CCCGGGCCTGAGGAATCC________________GGCTTAAGCCAGCGCCGCGGCCGGACAGTTA CGGCTACCCTCAGCCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:31457341..31457406 26863196 MeRIP-seq:(Medium) rs1393967236 Functional Loss DEL dbSNP153 19..34 33 - - - 83042 RMVar_ID_83042 Human_SNP_ID_549995916 m1A Human chr14 + 31457392 31457392 31457392 CCCGGGCCTGAGGAATCCGGCTACCCTCAGCCATGGCTTAAGCCAGCGCCGCGGCCGGACAGTTA CCCGGGCCTGAGGAATCCGGCTACCCTCAGCCGTGGCTTAAGCCAGCGCCGCGGCCGGACAGTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:31457341..31457406 26863196 MeRIP-seq:(Medium) rs914490641 Functional Loss SNV dbSNP153 33..33 33 - - - 83043 RMVar_ID_83043 Human_SNP_ID_550148960 m1A Human chr14 - 32077142 32077139 32077142 ACCAGCGGCGGCCCGTCCCTCCCCCCTTCCCCAGCGCCCGCCGCCGCGCCGGGCTCAGTAATGGC ACCAGCGGCGGCCCGTCCCTCCCCCCTTCCCC___GCCCGCCGCCGCGCCGGGCTCAGTAATGGC CGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:32077012..32077155 26863196 MeRIP-seq:(Medium) rs201487559 Functional Loss DEL dbSNP153 33..35 33 - - - 83044 RMVar_ID_83044 Human_SNP_ID_550149042 m1A Human chr14 + 32077330 32077327 32077330 CGCGCCGAGGAAGAGAGGCGAGCGGAGAGTGGAGGAGGAGGCGGCGGCGGCGGGAGCGGTCCCCA CGCGCCGAGGAAGAGAGGCGAGCGGAGAGT___GGAGGAGGCGGCGGCGGCGGGAGCGGTCCCCA TGGA T ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:32077292..32077425 26863196 MeRIP-seq:(Medium) rs767225867 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1065695,Human_RBP_ID_3467956,Human_RBP_ID_4292139,Human_RBP_ID_5315647,Human_RBP_ID_8180882,Human_RBP_ID_8725820,Human_RBP_ID_9418191,Human_RBP_ID_22711405,Human_RBP_ID_22926454,Human_RBP_ID_26778375 RMVar_hsa_circ_75556,RMVar_hsa_circ_165785,RMVar_hsa_circ_165786 83045 RMVar_ID_83045 Human_SNP_ID_550149044 m1A Human chr14 + 32077330 32077330 32077330 CGCGCCGAGGAAGAGAGGCGAGCGGAGAGTGGAGGAGGAGGCGGCGGCGGCGGGAGCGGTCCCCA CGCGCCGAGGAAGAGAGGCGAGCGGAGAGTGGTGGAGGAGGCGGCGGCGGCGGGAGCGGTCCCCA A T ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:32077292..32077425 26863196 MeRIP-seq:(Medium) rs1359961396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065695,Human_RBP_ID_3467956,Human_RBP_ID_4292139,Human_RBP_ID_5315647,Human_RBP_ID_8180882,Human_RBP_ID_8725820,Human_RBP_ID_9418191,Human_RBP_ID_22711405,Human_RBP_ID_22926454,Human_RBP_ID_26778375 RMVar_hsa_circ_75556,RMVar_hsa_circ_165785,RMVar_hsa_circ_165786 83046 RMVar_ID_83046 Human_SNP_ID_550149064 m1A Human chr14 - 32077357 32077357 32077357 CGGCGGTGGCGGCGGCAGCGACATTCCTGGGGACCGCTCCCGCCGCCGCCGCCTCCTCCTCCACT CGGCGGTGGCGGCGGCAGCGACATTCCTGGGGTCCGCTCCCGCCGCCGCCGCCTCCTCCTCCACT T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:32077192..32077378 26863410 MeRIP-seq:(Medium) rs895254483 Functional Loss SNV dbSNP153 33..33 33 - - - 83047 RMVar_ID_83047 Human_SNP_ID_550149065 m1A Human chr14 - 32077357 32077357 32077357 CGGCGGTGGCGGCGGCAGCGACATTCCTGGGGACCGCTCCCGCCGCCGCCGCCTCCTCCTCCACT CGGCGGTGGCGGCGGCAGCGACATTCCTGGGGCCCGCTCCCGCCGCCGCCGCCTCCTCCTCCACT T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:32077192..32077378 26863410 MeRIP-seq:(Medium) rs895254483 Functional Loss SNV dbSNP153 33..33 33 - - - 83048 RMVar_ID_83048 Human_SNP_ID_550149093 m1A Human chr14 + 32077405 32077403 32077406 TGCCGCCGCCACCGCCGGGGCCGCTGCCGTTGAGGAGGAGACGGAGGAGACCGACGTTGTTAGGT TGCCGCCGCCACCGCCGGGGCCGCTGCCGTT___GAGGAGACGGAGGAGACCGACGTTGTTAGGT TGAG T ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:32076331..32090581 26863196 MeRIP-seq:(Medium) rs765557119 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_231098,Human_RBP_ID_444708,Human_RBP_ID_756953,Human_RBP_ID_813203,Human_RBP_ID_882711,Human_RBP_ID_1065696,Human_RBP_ID_1171837,Human_RBP_ID_3467957,Human_RBP_ID_4307882,Human_RBP_ID_5176840,Human_RBP_ID_5236029,Human_RBP_ID_6340911,Human_RBP_ID_8181697,Human_RBP_ID_9324031,Human_RBP_ID_9418192,Human_RBP_ID_22926346,Human_RBP_ID_23619321 Human_Splice_Rec_1505631,Human_Splice_Rec_1505647,Human_Splice_Rec_1505659 Human_miRNA_ID_3122123 RMVar_hsa_circ_75556,RMVar_hsa_circ_165785,RMVar_hsa_circ_165786 83049 RMVar_ID_83049 Human_SNP_ID_550156494 m1A Human chr14 + 32108057 32108057 32108057 ATCAAGTGTTTAGGGAGGAAGTTCAAGAAAGAATGTTGCTGAGAGATCAAGGATGAAGAAAAAAG ATCAAGTGTTTAGGGAGGAAGTTCAAGAAAGAGTGTTGCTGAGAGATCAAGGATGAAGAAAAAAG A G ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:32108054..32108478 26863196 MeRIP-seq:(Medium) rs1413090057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9763705,Human_RBP_ID_23272465,Human_RBP_ID_23619384 RMVar_hsa_circ_278522,RMVar_hsa_circ_75556,RMVar_hsa_circ_356122,RMVar_hsa_circ_165786,RMVar_hsa_circ_339101,RMVar_hsa_circ_280324,RMVar_hsa_circ_165789,RMVar_hsa_circ_165790,RMVar_hsa_circ_165788 83050 RMVar_ID_83050 Human_SNP_ID_550247443 m1A Human chr14 - 32484957 32484957 32484957 TCAACGCTTCAATCTACTTCTCCCGCCGCAGGAAAAAAAGGCGGGAGAAGCCCCGCCAGGTTTGA TCAACGCTTCAATCTACTTCTCCCGCCGCAGGGAAAAAAGGCGGGAGAAGCCCCGCCAGGTTTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:32484922..32485058 26863196 MeRIP-seq:(Medium) rs796769414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5236190 83051 RMVar_ID_83051 Human_SNP_ID_550328623 m1A Human chr14 + 32821942 32821942 32821942 TTGTCAGTGAAGGAGACACAGAAACCACTACCAACTCTGAAATGTGCTTGCTCAATGCAGTGGAT TTGTCAGTGAAGGAGACACAGAAACCACTACCGACTCTGAAATGTGCTTGCTCAATGCAGTGGAT A G AKAP6 Ensembl:ENSG00000151320 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:32821896..32822023 26863196 MeRIP-seq:(Medium) rs1279651104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36897,RMVar_hsa_circ_165823,RMVar_hsa_circ_277053 83052 RMVar_ID_83052 Human_SNP_ID_550730016 m1A Human chr14 - 34435273 34435273 34435273 GATTCCATGCTGGTTTCCATTGTGGGGATGGCACTATACACAGGATACGTCTTCATGCCCCAGCA GATTCCATGCTGGTTTCCATTGTGGGGATGGCGCTATACACAGGATACGTCTTCATGCCCCAGCA T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:34435151..34435325 26863196 MeRIP-seq:(Medium) rs1194615804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_444900,Human_RBP_ID_1492954,Human_RBP_ID_4312273,Human_RBP_ID_17847631,Human_RBP_ID_22438700,Human_RBP_ID_23620097,Human_RBP_ID_24471303,Human_RBP_ID_26808019 Human_Splice_Rec_1506064 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 83053 RMVar_ID_83053 Human_SNP_ID_550731331 m1A Human chr14 + 34441611 34441611 34441611 GCCAGGAAGAAGAGGTAAACCTAAAGTTTGGGATTTTTTTTTCTCCTTTCTCCTTTTCTTTTCTG GCCAGGAAGAAGAGGTAAACCTAAAGTTTGGGGTTTTTTTTTCTCCTTTCTCCTTTTCTTTTCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:34441606..34441855 26863196 MeRIP-seq:(Medium) rs913228468 Functional Loss SNV dbSNP153 33..33 33 - - - 83054 RMVar_ID_83054 Human_SNP_ID_550731332 m1A Human chr14 + 34441611 34441611 34441611 GCCAGGAAGAAGAGGTAAACCTAAAGTTTGGGATTTTTTTTTCTCCTTTCTCCTTTTCTTTTCTG GCCAGGAAGAAGAGGTAAACCTAAAGTTTGGGTTTTTTTTTTCTCCTTTCTCCTTTTCTTTTCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:34441606..34441855 26863196 MeRIP-seq:(Medium) rs913228468 Functional Loss SNV dbSNP153 33..33 33 - - - 83055 RMVar_ID_83055 Human_SNP_ID_550737016 m1A Human chr14 - 34462177 34462177 34462177 GCATGGCGGGGATGGCGCTGGCGCGGGCCTGGAAGCAGATGTCCTGGTTCTACTACCAGTACCTG GCATGGCGGGGATGGCGCTGGCGCGGGCCTGGTAGCAGATGTCCTGGTTCTACTACCAGTACCTG T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:34462048..34462250 26863196 MeRIP-seq:(Medium) rs1425231517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231260,Human_RBP_ID_444910,Human_RBP_ID_757288,Human_RBP_ID_813347,Human_RBP_ID_1492961,Human_RBP_ID_4308263,Human_RBP_ID_5315648,Human_RBP_ID_17856614,Human_RBP_ID_18417936,Human_RBP_ID_22438702,Human_RBP_ID_22926217,Human_RBP_ID_23118299 Human_Splice_Rec_1506063 Human_miRNA_ID_2627060,Human_miRNA_ID_2747889 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 83056 RMVar_ID_83056 Human_SNP_ID_550737018 m1A Human chr14 + 34462180 34462180 34462180 GTACTGGTAGTAGAACCAGGACATCTGCTTCCAGGCCCGCGCCAGCGCCATCCCCGCCATGCGCC GTACTGGTAGTAGAACCAGGACATCTGCTTCCCGGCCCGCGCCAGCGCCATCCCCGCCATGCGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:34461949..34462294;chr14:34461926..34462275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 83057 RMVar_ID_83057 Human_SNP_ID_550740430 m1A Human chr14 - 34475428 34475418 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG__________GGAGAGGGAGAGGGAGAGGGAGA CCTCTCGCCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431666 Functional Loss DEL dbSNP153 33..42 33 - - - 83058 RMVar_ID_83058 Human_SNP_ID_550740432 m1A Human chr14 - 34475428 34475419 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG_________GGGAGAGGGAGAGGGAGAGGGAGA CTCTCGCCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431671 Functional Loss DEL dbSNP153 33..41 33 - - - 83059 RMVar_ID_83059 Human_SNP_ID_550740438 m1A Human chr14 - 34475428 34475421 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG_______GAGGGAGAGGGAGAGGGAGAGGGAGA CTCGCCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431685 Functional Loss DEL dbSNP153 33..39 33 - - - 83060 RMVar_ID_83060 Human_SNP_ID_550740442 m1A Human chr14 - 34475428 34475422 34475429 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGG_______AGAGGGAGAGGGAGAGGGAGAGGGAGA TCGCCCTC T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431688 Functional Loss DEL dbSNP153 32..38 33 - - - 83061 RMVar_ID_83061 Human_SNP_ID_550740446 m1A Human chr14 - 34475428 34475423 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG_____GAGAGGGAGAGGGAGAGGGAGAGGGAGA CGCCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431702 Functional Loss DEL dbSNP153 33..37 33 - - - 83062 RMVar_ID_83062 Human_SNP_ID_550740447 m1A Human chr14 - 34475428 34475424 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG____CGAGAGGGAGAGGGAGAGGGAGAGGGAGA GCCCT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431707 Functional Loss DEL dbSNP153 33..36 33 - - - 83063 RMVar_ID_83063 Human_SNP_ID_550740448 m1A Human chr14 - 34475428 34475424 34475429 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGG_____CGAGAGGGAGAGGGAGAGGGAGAGGGAGA GCCCTC G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431709 Functional Loss DEL dbSNP153 32..36 33 - - - 83064 RMVar_ID_83064 Human_SNP_ID_550740449 m1A Human chr14 - 34475434 34475424 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG__________CGAGAGGGAGAGGGAGAGGGAGA GCCCTCCCCCT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1566431710 Functional Loss DEL dbSNP153 33..42 33 - - - 83065 RMVar_ID_83065 Human_SNP_ID_550740450 m1A Human chr14 - 34475434 34475424 34475435 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGG___________CGAGAGGGAGAGGGAGAGGGAGA GCCCTCCCCCTC G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1566431711 Functional Loss DEL dbSNP153 32..42 33 - - - 83066 RMVar_ID_83066 Human_SNP_ID_550740455 m1A Human chr14 - 34475434 34475425 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG_________GCGAGAGGGAGAGGGAGAGGGAGA CCCTCCCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1395307204 Functional Loss DEL dbSNP153 33..41 33 - - - 83067 RMVar_ID_83067 Human_SNP_ID_550740456 m1A Human chr14 - 34475428 34475425 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG___GCGAGAGGGAGAGGGAGAGGGAGAGGGAGA CCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431715 Functional Loss DEL dbSNP153 33..35 33 - - - 83068 RMVar_ID_83068 Human_SNP_ID_550740458 m1A Human chr14 - 34475434 34475426 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG________GGCGAGAGGGAGAGGGAGAGGGAGA CCTCCCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1566431721 Functional Loss DEL dbSNP153 33..40 33 - - - 83069 RMVar_ID_83069 Human_SNP_ID_550740459 m1A Human chr14 - 34475428 34475426 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG__GGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA CCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431719 Functional Loss DEL dbSNP153 33..34 33 - - - 83070 RMVar_ID_83070 Human_SNP_ID_550740461 m1A Human chr14 - 34475428 34475427 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGG_GGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs1566431727 Functional Loss DEL dbSNP153 33..33 33 - - - 83071 RMVar_ID_83071 Human_SNP_ID_550740462 m1A Human chr14 - 34475434 34475427 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG_______GGGCGAGAGGGAGAGGGAGAGGGAGA CTCCCCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1566431729 Functional Loss DEL dbSNP153 33..39 33 - - - 83072 RMVar_ID_83072 Human_SNP_ID_550740463 m1A Human chr14 - 34475428 34475428 34475428 TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA TGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGGGGGCGAGAGGGAGAGGGAGAGGGAGAGGGAGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:34475420..34475535 26863196 MeRIP-seq:(Medium) rs993603595 Functional Loss SNV dbSNP153 33..33 33 - - - 83073 RMVar_ID_83073 Human_SNP_ID_550740471 m1A Human chr14 - 34475434 34475431 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG___GGGAGGGCGAGAGGGAGAGGGAGAGGGAGA CCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1566431740 Functional Loss DEL dbSNP153 33..35 33 - - - 83074 RMVar_ID_83074 Human_SNP_ID_550740472 m1A Human chr14 - 34475434 34475432 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG__GGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA CCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1336414118 Functional Loss DEL dbSNP153 33..34 33 - - - 83075 RMVar_ID_83075 Human_SNP_ID_550740473 m1A Human chr14 - 34475434 34475433 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGG_GGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs1233548613 Functional Loss DEL dbSNP153 33..33 33 - - - 83076 RMVar_ID_83076 Human_SNP_ID_550740474 m1A Human chr14 - 34475434 34475434 34475434 AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGAGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA AGACCATGGGGCGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGCGAGAGGGAGAGGGAGAGGGAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr14:34475413..34475546;chr14:34475426..34475475 26863196 MeRIP-seq:(Medium) rs796265604 Functional Loss SNV dbSNP153 33..33 33 - - - 83077 RMVar_ID_83077 Human_SNP_ID_550752219 m1A Human chr14 - 34516465 34516465 34516465 AGAACAGGAAGAAAAGGCGGGTCCATAAGAAGATGAGGTCTAACCGGGAAGATGCTGCCGAGAAG AGAACAGGAAGAAAAGGCGGGTCCATAAGAAGGTGAGGTCTAACCGGGAAGATGCTGCCGAGAAG T C EAPP Ensembl:ENSG00000129518 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:34516415..34516529 26863196 MeRIP-seq:(Medium) rs1157179921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_444922,Human_RBP_ID_9368775,Human_RBP_ID_17856395,Human_RBP_ID_26324677,Human_RBP_ID_27808202 83078 RMVar_ID_83078 Human_SNP_ID_550757563 m1A Human chr14 - 34536258 34536258 34536258 TTAAATGTATGCTAGCTCTGAGGATGAAGTGGATGTGCTTTTACATGGAACTCCTGACCAAAAAC TTAAATGTATGCTAGCTCTGAGGATGAAGTGGGTGTGCTTTTACATGGAACTCCTGACCAAAAAC T C EAPP Ensembl:ENSG00000129518 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:34536207..34536307 32194978 MeRIP-seq:(Medium) rs779767989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1818226,Human_RBP_ID_5463326,Human_RBP_ID_6342210,Human_RBP_ID_23620165,Human_RBP_ID_27808203 Human_Splice_Rec_1506066,Human_Splice_Rec_1506076,Human_Splice_Rec_1506096 RMVar_hsa_circ_165854,RMVar_hsa_circ_332246,RMVar_hsa_circ_165855,RMVar_hsa_circ_342912,RMVar_hsa_circ_325592 83079 RMVar_ID_83079 Human_SNP_ID_550762659 m1A Human chr14 - 34562902 34562902 34562902 ATGCCGCACTGTGTTCCCCATGACAGTGGTCCATCATCGTGCACTCGTCATACTCAGAAGTCCAA ATGCCGCACTGTGTTCCCCATGACAGTGGTCCGTCATCGTGCACTCGTCATACTCAGAAGTCCAA T C SNX6 Ensembl:ENSG00000129515 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:34562851..34563050 32194978 MeRIP-seq:(Medium) rs560016136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6342246,Human_RBP_ID_12318924,Human_RBP_ID_17247070,Human_RBP_ID_17361876,Human_RBP_ID_17478890,Human_RBP_ID_18649656,Human_RBP_ID_26428372,Human_RBP_ID_26808022 RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_92457,RMVar_hsa_circ_165860,RMVar_hsa_circ_83433,RMVar_hsa_circ_86040,RMVar_hsa_circ_165862,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_165863,RMVar_hsa_circ_165861,RMVar_hsa_circ_165858,RMVar_hsa_circ_165859 83080 RMVar_ID_83080 Human_SNP_ID_550803868 m1A Human chr14 + 34714597 34714594 34714597 GGCAGCTCGGGCTTCGGCTCTGTGGCACTGGGAGGAGAAGGAGGGGCGGGCGAGCGGGTGGGCAG GGCAGCTCGGGCTTCGGCTCTGTGGCACTG___GGAGAAGGAGGGGCGGGCGAGCGGGTGGGCAG GGGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:34714474..34714755 26863196 MeRIP-seq:(Medium) rs1428610020 Functional Loss DEL dbSNP153 31..33 33 - - - 83081 RMVar_ID_83081 Human_SNP_ID_550803879 m1A Human chr14 + 34714606 34714606 34714606 GGCTTCGGCTCTGTGGCACTGGGAGGAGAAGGAGGGGCGGGCGAGCGGGTGGGCAGCGGAGAGTG GGCTTCGGCTCTGTGGCACTGGGAGGAGAAGGTGGGGCGGGCGAGCGGGTGGGCAGCGGAGAGTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:34714483..34714693 26863196 MeRIP-seq:(Medium) rs1205023457 Functional Loss SNV dbSNP153 33..33 33 - - - 83082 RMVar_ID_83082 Human_SNP_ID_550817485 m1A Human chr14 - 34764785 34764785 34764785 GGGAGGTGAGGATGATGAAGTTGATGGCGATGAAGAAGAAGGTCAAAGTGAGGAGGAAGAGTATG GGGAGGTGAGGATGATGAAGTTGATGGCGATGGAGAAGAAGGTCAAAGTGAGGAGGAAGAGTATG T C BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:34764735..34764870 26863196 MeRIP-seq:(Medium) rs1220337375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813831,Human_RBP_ID_2411926,Human_RBP_ID_5522677,Human_RBP_ID_6342602,Human_RBP_ID_22737481,Human_RBP_ID_22926462,Human_RBP_ID_24543821 Human_Splice_Rec_1506395,Human_Splice_Rec_1506443,Human_Splice_Rec_1506491 RMVar_hsa_circ_116030,RMVar_hsa_circ_88530,RMVar_hsa_circ_165883,RMVar_hsa_circ_338990,RMVar_hsa_circ_366461,RMVar_hsa_circ_271486,RMVar_hsa_circ_60874,RMVar_hsa_circ_83760,RMVar_hsa_circ_99897,RMVar_hsa_circ_165889,RMVar_hsa_circ_165890,RMVar_hsa_circ_165888,RMVar_hsa_circ_165892,RMVar_hsa_circ_365684,RMVar_hsa_circ_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,RMVar_hsa_circ_165893 83083 RMVar_ID_83083 Human_SNP_ID_550817487 m1A Human chr14 - 34764788 34764788 34764788 TATGGGAGGTGAGGATGATGAAGTTGATGGCGATGAAGAAGAAGGTCAAAGTGAGGAGGAAGAGT TATGGGAGGTGAGGATGATGAAGTTGATGGCGTTGAAGAAGAAGGTCAAAGTGAGGAGGAAGAGT T A BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:34764693..34764954 26863196 MeRIP-seq:(Medium) rs764143855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813831,Human_RBP_ID_2411926,Human_RBP_ID_4292622,Human_RBP_ID_5522677,Human_RBP_ID_6342602,Human_RBP_ID_22737481,Human_RBP_ID_22926462,Human_RBP_ID_24543821,Human_RBP_ID_26325740 Human_Splice_Rec_1506395,Human_Splice_Rec_1506443,Human_Splice_Rec_1506491 RMVar_hsa_circ_116030,RMVar_hsa_circ_88530,RMVar_hsa_circ_165883,RMVar_hsa_circ_338990,RMVar_hsa_circ_366461,RMVar_hsa_circ_271486,RMVar_hsa_circ_60874,RMVar_hsa_circ_83760,RMVar_hsa_circ_99897,RMVar_hsa_circ_165889,RMVar_hsa_circ_165890,RMVar_hsa_circ_165888,RMVar_hsa_circ_165892,RMVar_hsa_circ_365684,RMVar_hsa_circ_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,RMVar_hsa_circ_165893 83084 RMVar_ID_83084 Human_SNP_ID_550824744 m1A Human chr14 - 34795760 34795760 34795760 TTGTTATTAACTTTTAAAAATTTCTAGGAAAGAGAGAAGTTACGTGAAGAAAAGCGAAAGTATGT TTGTTATTAACTTTTAAAAATTTCTAGGAAAGGGAGAAGTTACGTGAAGAAAAGCGAAAGTATGT T C BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:34795651..34795815 26863196 MeRIP-seq:(Medium) rs1266364302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40391,Human_RBP_ID_260661,Human_RBP_ID_880511,Human_RBP_ID_1502451,Human_RBP_ID_3944481,Human_RBP_ID_18189472,Human_RBP_ID_22578234,Human_RBP_ID_23620317,Human_RBP_ID_24543824,Human_RBP_ID_26325000,Human_RBP_ID_27808212 Human_Splice_Rec_1506370,Human_Splice_Rec_1506371,Human_Splice_Rec_1506420,Human_Splice_Rec_1506421,Human_Splice_Rec_1506466,Human_Splice_Rec_1506467 RMVar_hsa_circ_9117,RMVar_hsa_circ_83760,RMVar_hsa_circ_99897,RMVar_hsa_circ_165889,RMVar_hsa_circ_165890,RMVar_hsa_circ_165892,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_78973,RMVar_hsa_circ_120786,RMVar_hsa_circ_165893,RMVar_hsa_circ_361080,RMVar_hsa_circ_372223,RMVar_hsa_circ_165894,RMVar_hsa_circ_165895,RMVar_hsa_circ_31896,RMVar_hsa_circ_115563,RMVar_hsa_circ_165901,RMVar_hsa_circ_165902,RMVar_hsa_circ_300843,RMVar_hsa_circ_27862,RMVar_hsa_circ_312243,RMVar_hsa_circ_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_350573,RMVar_hsa_circ_112853,RMVar_hsa_circ_92854,RMVar_hsa_circ_165906,RMVar_hsa_circ_40039,RMVar_hsa_circ_165907,RMVar_hsa_circ_352615,RMVar_hsa_circ_165905,RMVar_hsa_circ_316848,RMVar_hsa_circ_37411,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_329638,RMVar_hsa_circ_365927,RMVar_hsa_circ_165908,RMVar_hsa_circ_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341 83085 RMVar_ID_83085 Human_SNP_ID_550825866 m1A Human chr14 - 34800294 34800294 34800294 AGAAGATAAAGAGAAAAAGAGGGAAGAATTGAAAAAAATTGTTGAAGAAGAGAGACTAAAGAAAA AGAAGATAAAGAGAAAAAGAGGGAAGAATTGATAAAAATTGTTGAAGAAGAGAGACTAAAGAAAA T A BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:34800185..34800400;chr14:34795676..34800400;chr14:34795651..34801100 26863196 MeRIP-seq:(Medium) rs1464607844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40393,Human_RBP_ID_197006,Human_RBP_ID_3447441,Human_RBP_ID_4292701,Human_RBP_ID_24543658,Human_RBP_ID_24551544 Human_Splice_Rec_1506368,Human_Splice_Rec_1506369,Human_Splice_Rec_1506418,Human_Splice_Rec_1506419,Human_Splice_Rec_1506464,Human_Splice_Rec_1506465 RMVar_hsa_circ_9117,RMVar_hsa_circ_83760,RMVar_hsa_circ_165890,RMVar_hsa_circ_165892,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_78973,RMVar_hsa_circ_120786,RMVar_hsa_circ_165893,RMVar_hsa_circ_372223,RMVar_hsa_circ_165894,RMVar_hsa_circ_165895,RMVar_hsa_circ_31896,RMVar_hsa_circ_115563,RMVar_hsa_circ_165901,RMVar_hsa_circ_165902,RMVar_hsa_circ_312243,RMVar_hsa_circ_14911,RMVar_hsa_circ_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_112853,RMVar_hsa_circ_92854,RMVar_hsa_circ_165906,RMVar_hsa_circ_40039,RMVar_hsa_circ_165907,RMVar_hsa_circ_352615,RMVar_hsa_circ_165905,RMVar_hsa_circ_37411,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365927,RMVar_hsa_circ_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341,RMVar_hsa_circ_70922,RMVar_hsa_circ_311650,RMVar_hsa_circ_332865,RMVar_hsa_circ_271761,RMVar_hsa_circ_69834,RMVar_hsa_circ_165912,RMVar_hsa_circ_165913,RMVar_hsa_circ_165914 83086 RMVar_ID_83086 Human_SNP_ID_550844501 m1A Human chr14 + 34874552 34874552 34874552 CTTTACAGTAGAAAACTTCCTCGTCGGGCCGCAGGTCCGCGGGCGGCTTCTGTCTCACAAACGGC CTTTACAGTAGAAAACTTCCTCGTCGGGCCGCGGGTCCGCGGGCGGCTTCTGTCTCACAAACGGC A G AL121603.2 Ensembl:ENSG00000258738 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:34874391..34874737 32194978 MeRIP-seq:(Medium) rs770728039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095521 83087 RMVar_ID_83087 Human_SNP_ID_550844564 m1A Human chr14 - 34874660 34874660 34874660 CCGGCTTTCCTTTCCCTCCAATTTTGATAGGGAAGCGGGGCCGGCGCGGGCGGCCGAGGGTCCAG CCGGCTTTCCTTTCCCTCCAATTTTGATAGGGGAGCGGGGCCGGCGCGGGCGGCCGAGGGTCCAG T C BAZ1A Ensembl:ENSG00000198604 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:34874501..34874773 26863196 MeRIP-seq:(Medium) rs891555911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231863,Human_RBP_ID_880514,Human_RBP_ID_5140855,Human_RBP_ID_5463785,Human_RBP_ID_9352993,Human_RBP_ID_17847749,Human_RBP_ID_18980540,Human_RBP_ID_19063940,Human_RBP_ID_22539946,Human_RBP_ID_27808217 Human_Splice_Rec_1506354,Human_Splice_Rec_1506404 RMVar_hsa_circ_264933,RMVar_hsa_circ_294174,RMVar_hsa_circ_115780,RMVar_hsa_circ_165925 83088 RMVar_ID_83088 Human_SNP_ID_550844763 m1A Human chr14 + 34875158 34875158 34875158 AGCGACCCTCACCTGCGATCACGCCGACTGCCACTTGTCCACCTTCTCCACTACAAAGGCAACGA AGCGACCCTCACCTGCGATCACGCCGACTGCCGCTTGTCCACCTTCTCCACTACAAAGGCAACGA A G AL121603.2 Ensembl:ENSG00000258738 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:34875129..34875278 32194978 MeRIP-seq:(Medium) rs1233142201 Functional Loss SNV dbSNP153 33..33 33 - - - 83089 RMVar_ID_83089 Human_SNP_ID_550844764 m1A Human chr14 + 34875158 34875158 34875158 AGCGACCCTCACCTGCGATCACGCCGACTGCCACTTGTCCACCTTCTCCACTACAAAGGCAACGA AGCGACCCTCACCTGCGATCACGCCGACTGCCTCTTGTCCACCTTCTCCACTACAAAGGCAACGA A T AL121603.2 Ensembl:ENSG00000258738 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:34875129..34875278 32194978 MeRIP-seq:(Medium) rs1233142201 Functional Loss SNV dbSNP153 33..33 33 - - - 83090 RMVar_ID_83090 Human_SNP_ID_550844776 m1A Human chr14 + 34875186 34875186 34875186 TGCCACTTGTCCACCTTCTCCACTACAAAGGCAACGAGGGGAGACCCCGTCCTCCCAGGGGACCG TGCCACTTGTCCACCTTCTCCACTACAAAGGCGACGAGGGGAGACCCCGTCCTCCCAGGGGACCG A G AL121603.2 Ensembl:ENSG00000258738 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:34875082..34875342 26863196 MeRIP-seq:(Medium) rs1291836964 Functional Loss SNV dbSNP153 33..33 33 - - - 83091 RMVar_ID_83091 Human_SNP_ID_550844829 m1A Human chr14 - 34875295 34875295 34875295 GGAGCTCCGAGAGGCGGGGAAGTGGCGGTGGGACGCAATTCCCCGCGCGGAGTCGGGCAGTGGCA GGAGCTCCGAGAGGCGGGGAAGTGGCGGTGGGGCGCAATTCCCCGCGCGGAGTCGGGCAGTGGCA T C BAZ1A Ensembl:ENSG00000198604 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:34874541..34875376;chr14:34875032..34875350;chr14:34875082..34875350;chr14:34874476..34875350;chr14:34874933..34875350 26863196 MeRIP-seq:(Medium) rs934182506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40999,Human_RBP_ID_4312386,Human_RBP_ID_9282162 83092 RMVar_ID_83092 Human_SNP_ID_550844832 m1A Human chr14 + 34875299 34875299 34875299 ACTGCCCGACTCCGCGCGGGGAATTGCGTCCCACCGCCACTTCCCCGCCTCTCGGAGCTCCTGGG ACTGCCCGACTCCGCGCGGGGAATTGCGTCCCCCCGCCACTTCCCCGCCTCTCGGAGCTCCTGGG A C AL121603.2 Ensembl:ENSG00000258738 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr14:34874982..34875351;chr14:34875089..34875351 26863196 MeRIP-seq:(Medium) rs987010354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882510 83093 RMVar_ID_83093 Human_SNP_ID_550885061 m1A Human chr14 - 35029221 35029220 35029221 AGAAAAATACACTTTCCCCCCAATTCGCAAAAAGAAGGGAAACGCTGAGGTCTCAGCAAATTAGG AGAAAAATACACTTTCCCCCCAATTCGCAAAA_GAAGGGAAACGCTGAGGTCTCAGCAAATTAGG CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35028146..35029221 32194978 MeRIP-seq:(Medium) rs1566659278 Functional Loss DEL dbSNP153 33..33 33 - - - 83094 RMVar_ID_83094 Human_SNP_ID_550889743 m1A Human chr14 + 35046530 35046530 35046530 TCACCAGCGCCAGCAGCCCTGTGGTGGCGACGACGATGGACCAGGAGCCAGTGGGCGGTGTGGAA TCACCAGCGCCAGCAGCCCTGTGGTGGCGACGTCGATGGACCAGGAGCCAGTGGGCGGTGTGGAA A T FAM177A1 Ensembl:ENSG00000151327 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:35046313..35046661;chr14:35046297..35046845;chr14:35046312..35046798;chr14:35046307..35046807 26863196 MeRIP-seq:(Medium) rs757742252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_445110,Human_RBP_ID_813268,Human_RBP_ID_882798,Human_RBP_ID_4308272,Human_RBP_ID_6343252,Human_RBP_ID_21886712,Human_RBP_ID_26325757 Human_Splice_Rec_1506742,Human_Splice_Rec_1506743,Human_Splice_Rec_1506754,Human_Splice_Rec_1506755,Human_Splice_Rec_1506758,Human_Splice_Rec_1506759,Human_Splice_Rec_1506767,Human_Splice_Rec_1506775,Human_Splice_Rec_1506779 Human_miRNA_ID_2083745,Human_miRNA_ID_2083746 RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_86978,RMVar_hsa_circ_165949,RMVar_hsa_circ_96949,RMVar_hsa_circ_313160,RMVar_hsa_circ_165950 83095 RMVar_ID_83095 Human_SNP_ID_550889753 m1A Human chr14 + 35046540 35046540 35046540 CAGCAGCCCTGTGGTGGCGACGACGATGGACCAGGAGCCAGTGGGCGGTGTGGAACGAGGAGAAG CAGCAGCCCTGTGGTGGCGACGACGATGGACCGGGAGCCAGTGGGCGGTGTGGAACGAGGAGAAG A G FAM177A1 Ensembl:ENSG00000151327 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:35046401..35046751 26863196 MeRIP-seq:(Medium) rs146253684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_445110,Human_RBP_ID_813268,Human_RBP_ID_882798,Human_RBP_ID_4308272,Human_RBP_ID_6343253,Human_RBP_ID_9324037,Human_RBP_ID_18435794,Human_RBP_ID_21886712,Human_RBP_ID_22495404,Human_RBP_ID_26325757 Human_Splice_Rec_1506742,Human_Splice_Rec_1506743,Human_Splice_Rec_1506754,Human_Splice_Rec_1506755,Human_Splice_Rec_1506758,Human_Splice_Rec_1506759,Human_Splice_Rec_1506767,Human_Splice_Rec_1506775,Human_Splice_Rec_1506779 Human_miRNA_ID_2083745,Human_miRNA_ID_2083746 RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_86978,RMVar_hsa_circ_165949,RMVar_hsa_circ_96949,RMVar_hsa_circ_313160,RMVar_hsa_circ_165950 83096 RMVar_ID_83096 Human_SNP_ID_550890700 m1A Human chr14 + 35049997 35049997 35049997 ACTTGCAGATTTATAAAATGAAGCATTTGGAAAATTCACAGTGTAACTTTTTTTGTTTTTTGAGA ACTTGCAGATTTATAAAATGAAGCATTTGGAACATTCACAGTGTAACTTTTTTTGTTTTTTGAGA A C FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:35049994..35050081 26863196 MeRIP-seq:(Medium) rs574113306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_313160 83097 RMVar_ID_83097 Human_SNP_ID_550891518 m1A Human chr14 + 35053221 35053221 35053221 TACAATAAACCTACCAAAAGTTTTTCACGTGTAATGAAAGAAAATTAATCTCACTTGAAACTCAT TACAATAAACCTACCAAAAGTTTTTCACGTGTCATGAAAGAAAATTAATCTCACTTGAAACTCAT A C FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:35053218..35053425;chr14:35053217..35053475 26863196 MeRIP-seq:(Medium) rs561907247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165951,RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_313160,RMVar_hsa_circ_302775 83098 RMVar_ID_83098 Human_SNP_ID_550905465 m1A Human chr14 + 35107252 35107252 35107252 GTAATCCCAACACCCAGTGATAACTACAGTTTACATTTTAGTGTCTATAAGAGTTAATATAATAT GTAATCCCAACACCCAGTGATAACTACAGTTTCCATTTTAGTGTCTATAAGAGTTAATATAATAT A C FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:35107237..35107407 26863410 MeRIP-seq:(Medium) rs10132769 Functional Loss SNV dbSNP153 33..33 33 - - - 83099 RMVar_ID_83099 Human_SNP_ID_550909275 m1A Human chr14 + 35122069 35122069 35122069 GCCAGGCCCCGTAAAGGTTAGGAAGGCCGTCCAACCACCATCTTGATCGAGGGCGGAAGTCTTGG GCCAGGCCCCGTAAAGGTTAGGAAGGCCGTCCCACCACCATCTTGATCGAGGGCGGAAGTCTTGG A C PRORP Ensembl:ENSG00000100890 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35122021..35122121 32194978 MeRIP-seq:(Medium) rs1381658852 Functional Loss SNV dbSNP153 33..33 33 - - - 83100 RMVar_ID_83100 Human_SNP_ID_550909367 m1A Human chr14 + 35122369 35122369 35122369 CTTTCACAATTTCTTTTCATTGTTCATTGCGGATATCTGGAAGCCTTCCAGGTCCCCTGAATGTA CTTTCACAATTTCTTTTCATTGTTCATTGCGGCTATCTGGAAGCCTTCCAGGTCCCCTGAATGTA A C PRORP Ensembl:ENSG00000100890 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35122318..35122418 32194978 MeRIP-seq:(Medium) rs935012378 Functional Loss SNV dbSNP153 33..33 33 - - - 83101 RMVar_ID_83101 Human_SNP_ID_550909476 m1A Human chr14 - 35122632 35122632 35122632 ACAGGAAGGGCGCTGCCTAGACTGCGTACCGAACGCTGACAAATGAAGTTCACTTCATTCAACAA ACAGGAAGGGCGCTGCCTAGACTGCGTACCGAGCGCTGACAAATGAAGTTCACTTCATTCAACAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:35122589..35122701 26863196 MeRIP-seq:(Medium) rs931130785 Functional Loss SNV dbSNP153 33..33 33 - - - 83102 RMVar_ID_83102 Human_SNP_ID_550913441 m1A Human chr14 + 35137585 35137585 35137585 CTTGAGGGGATGTCAAGATGCTAACTCAAGGCAGAAGGATTATGGCAGAGGGTGGGTGCTGAGGT CTTGAGGGGATGTCAAGATGCTAACTCAAGGCGGAAGGATTATGGCAGAGGGTGGGTGCTGAGGT A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:35137575..35137792 26863196 MeRIP-seq:(Medium) rs1292575194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49804,RMVar_hsa_circ_354649,RMVar_hsa_circ_276207,RMVar_hsa_circ_50510,RMVar_hsa_circ_165974 83103 RMVar_ID_83103 Human_SNP_ID_550944289 m1A Human chr14 - 35266875 35266875 35266875 AGTATAATTCACCTATTACCTCCAACACTTACATGTCATCAGCAAAAAAACAGCTGGCTTGCTTT AGTATAATTCACCTATTACCTCCAACACTTACGTGTCATCAGCAAAAAAACAGCTGGCTTGCTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35266850..35273461 32194978 MeRIP-seq:(Medium) rs1343357011 Functional Loss SNV dbSNP153 33..33 33 - - - 83104 RMVar_ID_83104 Human_SNP_ID_550950482 m1A Human chr14 - 35292452 35292452 35292452 CGGGACATGTTGGTAGAAGCACTACTTTAAACACAATCCCTGGGCCCCGTAGCTCCCGCACCAGG CGGGACATGTTGGTAGAAGCACTACTTTAAACGCAATCCCTGGGCCCCGTAGCTCCCGCACCAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:35292401..35292526 26863196 MeRIP-seq:(Medium) rs1377744283 Functional Loss SNV dbSNP153 33..33 33 - - - 83105 RMVar_ID_83105 Human_SNP_ID_550950484 m1A Human chr14 + 35292459 35292455 35292460 CGGGAGCTACGGGGCCCAGGGATTGTGTTTAAAGTAGTGCTTCTACCAACATGTCCCGTGGTTCC CGGGAGCTACGGGGCCCAGGGATTGTGTT_____TAGTGCTTCTACCAACATGTCCCGTGGTTCC TTAAAG T AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:35292376..35292527 26863196 MeRIP-seq:(Medium) rs756193813 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_1171929,Human_RBP_ID_1493132,Human_RBP_ID_4307890,Human_RBP_ID_5140856,Human_RBP_ID_5257901,Human_RBP_ID_5418112,Human_RBP_ID_5439022,Human_RBP_ID_5463330,Human_RBP_ID_8403279,Human_RBP_ID_9323764,Human_RBP_ID_17847841,Human_RBP_ID_22186007,Human_RBP_ID_22438703,Human_RBP_ID_23208515,Human_RBP_ID_27226499 Human_Splice_Rec_1507175,Human_Splice_Rec_1507177,Human_Splice_Rec_1507183,Human_Splice_Rec_1507193,Human_Splice_Rec_1507203,Human_Splice_Rec_1507215,Human_Splice_Rec_1507221,Human_Splice_Rec_1507231,Human_Splice_Rec_1507241,Human_Splice_Rec_1507243,Human_Splice_Rec_1507255,Human_Splice_Rec_1507277 RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 83106 RMVar_ID_83106 Human_SNP_ID_550950497 m1A Human chr14 - 35292485 35292485 35292485 GTAATGTGGCGGTCAAAACCGGCGCTGGAACCACGGGACATGTTGGTAGAAGCACTACTTTAAAC GTAATGTGGCGGTCAAAACCGGCGCTGGAACCCCGGGACATGTTGGTAGAAGCACTACTTTAAAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:35292434..35292526 26863196 MeRIP-seq:(Medium) rs781562053 Functional Loss SNV dbSNP153 33..33 33 - - - 83107 RMVar_ID_83107 Human_SNP_ID_550954423 m1A Human chr14 + 35308061 35308061 35308061 ACATCAGTAGCTGTCAGAGGGAAAGACTGTGCAGTAATTGTCACACAGAAGAAAGTACCTGTAAG ACATCAGTAGCTGTCAGAGGGAAAGACTGTGCGGTAATTGTCACACAGAAGAAAGTACCTGTAAG A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35308001..35312935 32194978 MeRIP-seq:(Medium) rs370118466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756499,Human_RBP_ID_883409,Human_RBP_ID_1493135,Human_RBP_ID_1818487,Human_RBP_ID_9324041,Human_RBP_ID_12323193,Human_RBP_ID_17248488,Human_RBP_ID_17856397,Human_RBP_ID_19063953,Human_RBP_ID_22439171,Human_RBP_ID_23620645 Human_Splice_Rec_1507152,Human_Splice_Rec_1507153,Human_Splice_Rec_1507164,Human_Splice_Rec_1507165,Human_Splice_Rec_1507178,Human_Splice_Rec_1507179,Human_Splice_Rec_1507204,Human_Splice_Rec_1507205,Human_Splice_Rec_1507216,Human_Splice_Rec_1507217,Human_Splice_Rec_1507222,Human_Splice_Rec_1507223,Human_Splice_Rec_1507232,Human_Splice_Rec_1507233,Human_Splice_Rec_1507242,Human_Splice_Rec_1507244,Human_Splice_Rec_1507245,Human_Splice_Rec_1507258,Human_Splice_Rec_1507259,Human_Splice_Rec_1507266,Human_Splice_Rec_1507267,Human_Splice_Rec_1507278,Human_Splice_Rec_1507279 RMVar_hsa_circ_298251,RMVar_hsa_circ_90474,RMVar_hsa_circ_318653,RMVar_hsa_circ_165976,RMVar_hsa_circ_338808,RMVar_hsa_circ_314965 83108 RMVar_ID_83108 Human_SNP_ID_550980096 m1A Human chr14 + 35402464 35402464 35402464 CATAGCTCTCCTCATCCTCACTCTCTGGCAGCATCTGAAGGTTTTCTAGTGTCAGCTGGCCCAGC CATAGCTCTCCTCATCCTCACTCTCTGGCAGCGTCTGAAGGTTTTCTAGTGTCAGCTGGCCCAGC A G lnc-INSM2-5 RNACentral:URS00008B8DC0 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:35402401..35402475 32194978 MeRIP-seq:(Medium) rs1457878328 Functional Loss SNV dbSNP153 33..33 33 - - - 83109 RMVar_ID_83109 Human_SNP_ID_550980626 m1A Human chr14 + 35403797 35403797 35403797 CTTTTCTTCATGGATGATGGCCAAGTGCAGGAACCTGTGGGGAAGAGAGGGAAAAACCCCAGGGG CTTTTCTTCATGGATGATGGCCAAGTGCAGGAGCCTGTGGGGAAGAGAGGGAAAAACCCCAGGGG A G lnc-INSM2-5 RNACentral:URS00008B8DC0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:35403790..35403877 26863196 MeRIP-seq:(Medium) rs1300312443 Functional Loss SNV dbSNP153 33..33 33 - - - 83110 RMVar_ID_83110 Human_SNP_ID_550980971 m1A Human chr14 - 35404551 35404551 35404551 AGAAGGAGCGGCTACTGGACGACCGCCACGACAGCGGCCTGGACTCCATGAAAGACGAGGAGTAC AGAAGGAGCGGCTACTGGACGACCGCCACGACGGCGGCCTGGACTCCATGAAAGACGAGGAGTAC T C NFKBIA Ensembl:ENSG00000100906 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:35404501..35404700 32194978 MeRIP-seq:(Medium) rs1566591086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758269,Human_RBP_ID_5140979,Human_RBP_ID_8230492,Human_RBP_ID_9369994,Human_RBP_ID_17857032,Human_RBP_ID_24543662,Human_RBP_ID_27808228 Human_Splice_Rec_1507353 Clinvar_Rec_431 83111 RMVar_ID_83111 Human_SNP_ID_550981005 m1A Human chr14 - 35404619 35404619 35404619 CCGCGCCATGTTCCAGGCGGCCGAGCGCCCCCAGGAGTGGGCCATGGAGGGCCCCCGCGACGGGC CCGCGCCATGTTCCAGGCGGCCGAGCGCCCCCGGGAGTGGGCCATGGAGGGCCCCCGCGACGGGC T C NFKBIA Ensembl:ENSG00000100906 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:35404576..35404725 26863196 MeRIP-seq:(Medium) rs1383874564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308277,Human_RBP_ID_5141099,Human_RBP_ID_17847879,Human_RBP_ID_24543662,Human_RBP_ID_27808229 83112 RMVar_ID_83112 Human_SNP_ID_550981059 m1A Human chr14 - 35404703 35404703 35404703 CGCCGTCCCGCCCGCCAGCGCCCCAGCGAGGAAGCAGCGCGCAGCCCGCGGCCCAGCGCACCCGC CGCCGTCCCGCCCGCCAGCGCCCCAGCGAGGAGGCAGCGCGCAGCCCGCGGCCCAGCGCACCCGC T C NFKBIA Ensembl:ENSG00000100906 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:35404676..35404750 26863196 MeRIP-seq:(Medium) rs1456076438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758271,Human_RBP_ID_4308277 83113 RMVar_ID_83113 Human_SNP_ID_551073144 m1A Human chr14 - 35809191 35809191 35809191 GAGAGAGTTGTGCTCCTGCCGCCGAGAGCTCCACCTTCGTGGCTCTGGGTCCGGGGCCCCGGCCT GAGAGAGTTGTGCTCCTGCCGCCGAGAGCTCCGCCTTCGTGGCTCTGGGTCCGGGGCCCCGGCCT T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:35809126..35809214 26863196 MeRIP-seq:(Medium) rs1228898871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757360,Human_RBP_ID_880915,Human_RBP_ID_1493208,Human_RBP_ID_4308724,Human_RBP_ID_5463723,Human_RBP_ID_22186036,Human_RBP_ID_26326251 RMVar_hsa_circ_78773,RMVar_hsa_circ_165985 83114 RMVar_ID_83114 Human_SNP_ID_551079114 m1A Human chr14 - 35832923 35832923 35832923 TGTTAATTTAAAAATCTCAACAAAGGCTAACAATTTGCCATTTCTATACATTATTTGTTCCCAAT TGTTAATTTAAAAATCTCAACAAAGGCTAACAGTTTGCCATTTCTATACATTATTTGTTCCCAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:35832921..35833012 26863196 MeRIP-seq:(Medium) rs139654728 Functional Loss SNV dbSNP153 33..33 33 - - - 83115 RMVar_ID_83115 Human_SNP_ID_551278467 m1A Human chr14 - 36662060 36662060 36662060 CATTGCTCCGAGCAGTACACCAACCCGGCCCCAGTTCCGCACTCCCAGACAGAAACTTTCCGCAC CATTGCTCCGAGCAGTACACCAACCCGGCCCCGGTTCCGCACTCCCAGACAGAAACTTTCCGCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:36662009..36662129 26863196 MeRIP-seq:(Medium) rs572384078 Functional Loss SNV dbSNP153 33..33 33 - - - 83116 RMVar_ID_83116 Human_SNP_ID_551278478 m1A Human chr14 - 36662079 36662079 36662079 TCCCCCGCCGCCACTCACCCATTGCTCCGAGCAGTACACCAACCCGGCCCCAGTTCCGCACTCCC TCCCCCGCCGCCACTCACCCATTGCTCCGAGCTGTACACCAACCCGGCCCCAGTTCCGCACTCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:36662028..36662129 26863196 MeRIP-seq:(Medium) rs1462661866 Functional Loss SNV dbSNP153 33..33 33 - - - 83117 RMVar_ID_83117 Human_SNP_ID_551300237 m1A Human chr14 + 36749768 36749768 36749768 TGGGATCCTCACCTCACAAAGCCGCAGGGCTCACTGTTCACCTCCTTCACATCTTTGCACAAACA TGGGATCCTCACCTCACAAAGCCGCAGGGCTCGCTGTTCACCTCCTTCACATCTTTGCACAAACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:36749740..36749808 26863196 MeRIP-seq:(Medium) rs1002548402 Functional Loss SNV dbSNP153 33..33 33 - - - 83118 RMVar_ID_83118 Human_SNP_ID_551504609 m1A Human chr14 + 37591621 37591621 37591621 GGTGGTTGAAGGAGTAGTGGGGGTCCCCTTTCAGGTGCAGCTGGGACTCGTGGGGTGCCAAGCCG GGTGGTTGAAGGAGTAGTGGGGGTCCCCTTTCGGGTGCAGCTGGGACTCGTGGGGTGCCAAGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:37591570..37591653 26863196 MeRIP-seq:(Medium) rs1334604520 Functional Loss SNV dbSNP153 33..33 33 - - - 83119 RMVar_ID_83119 Human_SNP_ID_551505761 m1A Human chr14 + 37594982 37594982 37594982 TCCATCTTCACAGTTCCTAACATCCTGGAGCCACCCTGCCCAATACAACCATCCAGCCCTGTGCG TCCATCTTCACAGTTCCTAACATCCTGGAGCCCCCCTGCCCAATACAACCATCCAGCCCTGTGCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:37594933..37595111 26863196 MeRIP-seq:(Medium) rs757567436 Functional Loss SNV dbSNP153 33..33 33 - - - 83120 RMVar_ID_83120 Human_SNP_ID_551505913 m1A Human chr14 - 37595292 37595292 37595292 CAAATGGGGAGAGGACGAGGAGGTGGGCACTCAAGCGACGTAAGATCCACATCAGCTCAACTGCA CAAATGGGGAGAGGACGAGGAGGTGGGCACTCTAGCGACGTAAGATCCACATCAGCTCAACTGCA T A FOXA1 Ensembl:ENSG00000129514 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:37595242..37595356 26863196 MeRIP-seq:(Medium) rs1263199637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1508530 83121 RMVar_ID_83121 Human_SNP_ID_551541973 m1A Human chr14 - 37746725 37746725 37746725 TAATGCACCTACCTCAAGCATGCCCTGAAATCACTCAGCTGTGACTCCCAAACCCTCTCATGGAG TAATGCACCTACCTCAAGCATGCCCTGAAATCCCTCAGCTGTGACTCCCAAACCCTCTCATGGAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:37746674..37746799 26863196 MeRIP-seq:(Medium) rs1453977748 Functional Loss SNV dbSNP153 33..33 33 - - - 83122 RMVar_ID_83122 Human_SNP_ID_551856498 m1A Human chr14 - 39032968 39032966 39032969 AAGTCTTTATAACTTAATTATGTTTAATAAAAAATAGAGTCTGCCTCGTACTACAGATGTAACTC AAGTCTTTATAACTTAATTATGTTTAATAAA___TAGAGTCTGCCTCGTACTACAGATGTAACTC ATTT A SEC23A Ensembl:ENSG00000100934 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:39032917..39033168 32194978 MeRIP-seq:(Medium) rs756390255 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1818854 RMVar_hsa_circ_104962,RMVar_hsa_circ_166063 83123 RMVar_ID_83123 Human_SNP_ID_551863581 m1A Human chr14 + 39061842 39061842 39061842 TGCTGATACTGAGTCACAAACTGGATTGCACCACGCCCTCCTTGAGGAATTGGAGCATTATGCTG TGCTGATACTGAGTCACAAACTGGATTGCACCGCGCCCTCCTTGAGGAATTGGAGCATTATGCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:39048686..39064555 32194978 MeRIP-seq:(Medium) rs1218436121 Functional Loss SNV dbSNP153 33..33 33 - - - 83124 RMVar_ID_83124 Human_SNP_ID_551867053 m1A Human chr14 - 39076002 39076002 39076002 GGGGCCTGGAATGGTGGTTGGAGATGAGTTGAAGACACCTATAAGATCGTGGCATGACATTGACA GGGGCCTGGAATGGTGGTTGGAGATGAGTTGACGACACCTATAAGATCGTGGCATGACATTGACA T G SEC23A Ensembl:ENSG00000100934 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:39075951..39087560 32194978 MeRIP-seq:(Medium) rs1245439317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757020,Human_RBP_ID_883802,Human_RBP_ID_1274924,Human_RBP_ID_3944896,Human_RBP_ID_12328760,Human_RBP_ID_17248493,Human_RBP_ID_17669338,Human_RBP_ID_23621722 Human_Splice_Rec_1508970,Human_Splice_Rec_1508971,Human_Splice_Rec_1509008,Human_Splice_Rec_1509009,Human_Splice_Rec_1509044,Human_Splice_Rec_1509045 RMVar_hsa_circ_1390,RMVar_hsa_circ_99660,RMVar_hsa_circ_73967,RMVar_hsa_circ_166066,RMVar_hsa_circ_364893,RMVar_hsa_circ_366537,RMVar_hsa_circ_301486,RMVar_hsa_circ_7111,RMVar_hsa_circ_166071,RMVar_hsa_circ_166072,RMVar_hsa_circ_21074,RMVar_hsa_circ_294171,RMVar_hsa_circ_166075,RMVar_hsa_circ_304276,RMVar_hsa_circ_377846,RMVar_hsa_circ_289078,RMVar_hsa_circ_108320,RMVar_hsa_circ_166077,RMVar_hsa_circ_166078,RMVar_hsa_circ_166076,RMVar_hsa_circ_166086,RMVar_hsa_circ_324222,RMVar_hsa_circ_359520,RMVar_hsa_circ_370700,RMVar_hsa_circ_294582,RMVar_hsa_circ_166087,RMVar_hsa_circ_166084,RMVar_hsa_circ_166085,RMVar_hsa_circ_39531,RMVar_hsa_circ_166088,RMVar_hsa_circ_36317,RMVar_hsa_circ_354866,RMVar_hsa_circ_357016,RMVar_hsa_circ_117105,RMVar_hsa_circ_166089,RMVar_hsa_circ_273689,RMVar_hsa_circ_336082,RMVar_hsa_circ_288155,RMVar_hsa_circ_88474,RMVar_hsa_circ_299405,RMVar_hsa_circ_48561,RMVar_hsa_circ_60356,RMVar_hsa_circ_166090,RMVar_hsa_circ_313769,RMVar_hsa_circ_336984,RMVar_hsa_circ_273139,RMVar_hsa_circ_291037,RMVar_hsa_circ_63052,RMVar_hsa_circ_166096,RMVar_hsa_circ_166092,RMVar_hsa_circ_166094,RMVar_hsa_circ_166095,RMVar_hsa_circ_166093,RMVar_hsa_circ_353861,RMVar_hsa_circ_166091,RMVar_hsa_circ_335319 83125 RMVar_ID_83125 Human_SNP_ID_551870627 m1A Human chr14 - 39089478 39089465 39089479 TAGGAAGACATAGTAGGGATTCCTTCAGGAGCACAGGAAGCGGAGTACCTTAGAGAGGAGAATCA TAGGAAGACATAGTAGGGATTCCTTCAGGAG______________TACCTTAGAGAGGAGAATCA ACTCCGCTTCCTGTG A SEC23A Ensembl:ENSG00000100934 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:39089476..39089573 26863196 MeRIP-seq:(Medium) rs570739892 Functional Loss DEL dbSNP153 32..45 33 - - - Human_RBP_ID_813753 RMVar_hsa_circ_38826,RMVar_hsa_circ_99660,RMVar_hsa_circ_73967,RMVar_hsa_circ_166066,RMVar_hsa_circ_301486,RMVar_hsa_circ_166072,RMVar_hsa_circ_294171,RMVar_hsa_circ_166075,RMVar_hsa_circ_377846,RMVar_hsa_circ_289078,RMVar_hsa_circ_108320,RMVar_hsa_circ_166077,RMVar_hsa_circ_166078,RMVar_hsa_circ_166076,RMVar_hsa_circ_166086,RMVar_hsa_circ_370700,RMVar_hsa_circ_166087,RMVar_hsa_circ_39531,RMVar_hsa_circ_166088,RMVar_hsa_circ_354866,RMVar_hsa_circ_117105,RMVar_hsa_circ_288155,RMVar_hsa_circ_88474,RMVar_hsa_circ_60356,RMVar_hsa_circ_166090,RMVar_hsa_circ_336984,RMVar_hsa_circ_291037,RMVar_hsa_circ_63052,RMVar_hsa_circ_166096,RMVar_hsa_circ_166094,RMVar_hsa_circ_166095,RMVar_hsa_circ_353861,RMVar_hsa_circ_335319,RMVar_hsa_circ_349655,RMVar_hsa_circ_376833,RMVar_hsa_circ_90778,RMVar_hsa_circ_366635,RMVar_hsa_circ_45179,RMVar_hsa_circ_166099 83126 RMVar_ID_83126 Human_SNP_ID_551872674 m1A Human chr14 - 39096044 39096044 39096044 GATGGAGTCCGATTTAGTTGGAATGTTTGGCCATCAAGTCGACTGGAAGCTACAAGAATGGTTGT GATGGAGTCCGATTTAGTTGGAATGTTTGGCCGTCAAGTCGACTGGAAGCTACAAGAATGGTTGT T C SEC23A Ensembl:ENSG00000100934 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:39095997..39103190 32194978 MeRIP-seq:(Medium) rs1462736736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39512,Human_RBP_ID_445560,Human_RBP_ID_1493442,Human_RBP_ID_1818873,Human_RBP_ID_18650336,Human_RBP_ID_23621766,Human_RBP_ID_26808463 Human_Splice_Rec_1508996,Human_Splice_Rec_1509034,Human_Splice_Rec_1509078,Human_Splice_Rec_1509088,Human_Splice_Rec_1509096,Human_Splice_Rec_1509102,Human_Splice_Rec_1509106,Human_Splice_Rec_1509110,Human_Splice_Rec_1509118 RMVar_hsa_circ_39531,RMVar_hsa_circ_166088,RMVar_hsa_circ_117105,RMVar_hsa_circ_353861,RMVar_hsa_circ_349655,RMVar_hsa_circ_45179,RMVar_hsa_circ_166102,RMVar_hsa_circ_166100,RMVar_hsa_circ_374003,RMVar_hsa_circ_166101,RMVar_hsa_circ_281670,RMVar_hsa_circ_306209 83127 RMVar_ID_83127 Human_SNP_ID_551874834 m1A Human chr14 + 39103385 39103385 39103385 AGGCGCGCGGCGGGCGAAGGTACCGAGAGGGGAGGAGGGAGGAGAGGTAGCGGGGACCGAGCCAG AGGCGCGCGGCGGGCGAAGGTACCGAGAGGGGGGGAGGGAGGAGAGGTAGCGGGGACCGAGCCAG A G SEC23A-AS1 Ensembl:ENSG00000258651 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:39103338..39103443 26863196 MeRIP-seq:(Medium) rs940869485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812981,Human_RBP_ID_5352204,Human_RBP_ID_9418206,Human_RBP_ID_18417945,Human_RBP_ID_22540320 83128 RMVar_ID_83128 Human_SNP_ID_551874849 m1A Human chr14 + 39103447 39103447 39103447 CAGAGGGGCGGAAGAACCCGGAAGACCCAGGCAGCCGGACGGCCGAGGGGCGTGGGACCGGGCAG CAGAGGGGCGGAAGAACCCGGAAGACCCAGGCTGCCGGACGGCCGAGGGGCGTGGGACCGGGCAG A T SEC23A-AS1 Ensembl:ENSG00000258651 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:39103338..39103489 26863196 MeRIP-seq:(Medium) rs1463326629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882564,Human_RBP_ID_5352204,Human_RBP_ID_5565193,Human_RBP_ID_23256293 83129 RMVar_ID_83129 Human_SNP_ID_551894343 m1A Human chr14 - 39175389 39175389 39175389 CGAGTTCCGAGTTCCCGTTAGGCCCTTACCTCACGTCATTCGGATCCCGCCCGGTGAGCTTGCGA CGAGTTCCGAGTTCCCGTTAGGCCCTTACCTCTCGTCATTCGGATCCCGCCCGGTGAGCTTGCGA T A AL132639.3 Ensembl:ENSG00000259083 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:39175251..39175832 26863196 MeRIP-seq:(Medium) rs757344324 Functional Loss SNV dbSNP153 33..33 33 - - - 83130 RMVar_ID_83130 Human_SNP_ID_551894618 m1A Human chr14 - 39176030 39176030 39176030 AAATCAGTGCAAAATCATATGTAGACACACACAGTCGCACCCAAATACTTTCAGAGATGTGGATC AAATCAGTGCAAAATCATATGTAGACACACACTGTCGCACCCAAATACTTTCAGAGATGTGGATC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:39176028..39176197 26863196 MeRIP-seq:(Medium) rs1486572897 Functional Loss SNV dbSNP153 33..33 33 - - - 83131 RMVar_ID_83131 Human_SNP_ID_551894794 m1A Human chr14 - 39176489 39176489 39176489 ATTTAAAATGTTCAACATAAAACACTTGAAATACAAGATAAATGGTATTTCCATTTGACAAGAGA ATTTAAAATGTTCAACATAAAACACTTGAAATGCAAGATAAATGGTATTTCCATTTGACAAGAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:39176486..39176634 26863196 MeRIP-seq:(Medium) rs1233625172 Functional Loss SNV dbSNP153 33..33 33 - - - 83132 RMVar_ID_83132 Human_SNP_ID_551894812 m1A Human chr14 - 39176537 39176537 39176537 CTGTTTGGCTGGGGGTCCTCCTCCACTATCTGAGAATCCACGCCTGAAATTTAAAATGTTCAACA CTGTTTGGCTGGGGGTCCTCCTCCACTATCTGGGAATCCACGCCTGAAATTTAAAATGTTCAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:39176526..39176600 26863196 MeRIP-seq:(Medium) rs1216182932 Functional Loss SNV dbSNP153 33..33 33 - - - 83133 RMVar_ID_83133 Human_SNP_ID_551894813 m1A Human chr14 + 39176539 39176539 39176539 TTGAACATTTTAAATTTCAGGCGTGGATTCTCAGATAGTGGAGGAGGACCCCCAGCCAAACAGAG TTGAACATTTTAAATTTCAGGCGTGGATTCTCCGATAGTGGAGGAGGACCCCCAGCCAAACAGAG A C PNN Ensembl:ENSG00000100941 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:39176526..39176600 26863196 MeRIP-seq:(Medium) rs774546727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40748,Human_RBP_ID_1493486,Human_RBP_ID_3944496,Human_RBP_ID_5463727,Human_RBP_ID_5566131,Human_RBP_ID_6347832,Human_RBP_ID_9368875,Human_RBP_ID_12329621,Human_RBP_ID_18650391,Human_RBP_ID_18979587,Human_RBP_ID_21969525,Human_RBP_ID_22577266,Human_RBP_ID_22737488,Human_RBP_ID_22797846,Human_RBP_ID_26325012,Human_RBP_ID_27808245 Human_Splice_Rec_1509342,Human_Splice_Rec_1509343,Human_Splice_Rec_1509352,Human_Splice_Rec_1509353,Human_Splice_Rec_1509358,Human_Splice_Rec_1509359 83134 RMVar_ID_83134 Human_SNP_ID_551895112 m1A Human chr14 + 39177442 39177442 39177442 AGGCTGGGCGGGGAGCGTCGGACCAGAAGAGAATCACGCCAGGAAAGCGACCCGGAGGATGATGA AGGCTGGGCGGGGAGCGTCGGACCAGAAGAGAGTCACGCCAGGAAAGCGACCCGGAGGATGATGA A G PNN Ensembl:ENSG00000100941 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:39176526..39177903 32194978 MeRIP-seq:(Medium) rs192899760 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_40749,Human_RBP_ID_881767,Human_RBP_ID_1493487,Human_RBP_ID_1818928,Human_RBP_ID_2413649,Human_RBP_ID_3944499,Human_RBP_ID_5563173,Human_RBP_ID_6347839,Human_RBP_ID_8403769,Human_RBP_ID_9368881,Human_RBP_ID_12329635,Human_RBP_ID_18469425,Human_RBP_ID_18980568,Human_RBP_ID_22649051,Human_RBP_ID_24543982,Human_RBP_ID_25123755,Human_RBP_ID_26325013,Human_RBP_ID_27808246 Human_Splice_Rec_1509344,Human_Splice_Rec_1509345,Human_Splice_Rec_1509354,Human_Splice_Rec_1509360,Human_Splice_Rec_1509361 RMVar_hsa_circ_166119,RMVar_hsa_circ_278906 83135 RMVar_ID_83135 Human_SNP_ID_551896264 m1A Human chr14 - 39180639 39180637 39180640 TCCTCCAACTCTTCCTCTCGCTGAGCCACCTTACCCTCTTCTTGTTCCGCCTTCTGTTCTTCATT TCCTCCAACTCTTCCTCTCGCTGAGCCACCT___CCTCTTCTTGTTCCGCCTTCTGTTCTTCATT GGTA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:39180588..39180824 26863196 MeRIP-seq:(Medium) rs747216206 Functional Loss DEL dbSNP153 32..34 33 - - - 83136 RMVar_ID_83136 Human_SNP_ID_551896277 m1A Human chr14 + 39180662 39180662 39180662 AGAAGAGGGTAAGGTGGCTCAGCGAGAGGAAGAGTTGGAGGAGACAGGTAATCAGCACAATGATG AGAAGAGGGTAAGGTGGCTCAGCGAGAGGAAGCGTTGGAGGAGACAGGTAATCAGCACAATGATG A C PNN Ensembl:ENSG00000100941 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:39180558..39180925 26863196 MeRIP-seq:(Medium) rs1228401421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40750,Human_RBP_ID_197008,Human_RBP_ID_231648,Human_RBP_ID_445682,Human_RBP_ID_881774,Human_RBP_ID_1493522,Human_RBP_ID_2413675,Human_RBP_ID_4293543,Human_RBP_ID_5563181,Human_RBP_ID_6347870,Human_RBP_ID_8250172,Human_RBP_ID_8403781,Human_RBP_ID_9368904,Human_RBP_ID_12329724,Human_RBP_ID_22737493,Human_RBP_ID_22926348,Human_RBP_ID_23113694,Human_RBP_ID_23118229,Human_RBP_ID_23621886,Human_RBP_ID_24543669,Human_RBP_ID_24551547,Human_RBP_ID_26325019,Human_RBP_ID_27808256 Human_Splice_Rec_1509381 RMVar_hsa_circ_166124 83137 RMVar_ID_83137 Human_SNP_ID_551896281 m1A Human chr14 - 39180681 39180681 39180681 CCTGCTTCCTCTATTTCTACATCATTGTGCTGATTACCTGTCTCCTCCAACTCTTCCTCTCGCTG CCTGCTTCCTCTATTTCTACATCATTGTGCTGGTTACCTGTCTCCTCCAACTCTTCCTCTCGCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:39180549..39180698 32194978 MeRIP-seq:(Medium) rs1065613 Functional Loss SNV dbSNP153 33..33 33 - - - 83138 RMVar_ID_83138 Human_SNP_ID_551896284 m1A Human chr14 - 39180690 39180690 39180690 TCTTCCTCTCCTGCTTCCTCTATTTCTACATCATTGTGCTGATTACCTGTCTCCTCCAACTCTTC TCTTCCTCTCCTGCTTCCTCTATTTCTACATCGTTGTGCTGATTACCTGTCTCCTCCAACTCTTC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:39180589..39180877 26863196 MeRIP-seq:(Medium) rs1290701871 Functional Loss SNV dbSNP153 33..33 33 - - - 83139 RMVar_ID_83139 Human_SNP_ID_551896313 m1A Human chr14 - 39180753 39180753 39180753 TTTTGTTCTTCCTCCTCCTGTTCTTTCTCTGCATCACTATGAACAATCGCTATTTCCTTTTCCTC TTTTGTTCTTCCTCCTCCTGTTCTTTCTCTGCGTCACTATGAACAATCGCTATTTCCTTTTCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:39180544..39180956;chr14:39180501..39181000 26863196 MeRIP-seq:(Medium) rs1338299018 Functional Loss SNV dbSNP153 33..33 33 - - - 83140 RMVar_ID_83140 Human_SNP_ID_551896659 m1A Human chr14 - 39181590 39181590 39181590 CGGCCCCTACTCCGACTTCTACTCTCACTACTACTACTAGTGCTACTGCTACTATCTCTGCTGCT CGGCCCCTACTCCGACTTCTACTCTCACTACTGCTACTAGTGCTACTGCTACTATCTCTGCTGCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:39181524..39181704 26863196 MeRIP-seq:(Medium) rs751860107 Functional Loss SNV dbSNP153 33..33 33 - - - 83141 RMVar_ID_83141 Human_SNP_ID_551944183 m1A Human chr14 - 39348955 39348955 39348955 AAAAGCATACTTGCAAATGGAGCAGGTGGTGGACCTGGGAAATCCCCTGGTGGAAAATAATCTCG AAAAGCATACTTGCAAATGGAGCAGGTGGTGGCCCTGGGAAATCCCCTGGTGGAAAATAATCTCG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:39348754..39348965 26863196 MeRIP-seq:(Medium) rs771093450 Functional Loss SNV dbSNP153 33..33 33 - - - 83142 RMVar_ID_83142 Human_SNP_ID_551966729 m1A Human chr14 + 39431760 39431760 39431760 GGCGGCGAATTCAACACGCAGCTCTCGCACGAACCAGCCGCACTTGCGCATGAGGAATTCCAGCC GGCGGCGAATTCAACACGCAGCTCTCGCACGACCCAGCCGCACTTGCGCATGAGGAATTCCAGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:39431709..39432154 26863196 MeRIP-seq:(Medium) rs548769964 Functional Loss SNV dbSNP153 33..33 33 - - - 83143 RMVar_ID_83143 Human_SNP_ID_551967002 m1A Human chr14 + 39432269 39432269 39432269 GGGAAAGGCCTCTGCGGGCGTGGCCTGCCGGGAGCCAGCCTCTGTCTTCTCAAACTCTACTCACG GGGAAAGGCCTCTGCGGGCGTGGCCTGCCGGGGGCCAGCCTCTGTCTTCTCAAACTCTACTCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:39432218..39432375 26863196 MeRIP-seq:(Medium) rs1049522650 Functional Loss SNV dbSNP153 33..33 33 - - - 83144 RMVar_ID_83144 Human_SNP_ID_551972741 m1A Human chr14 + 39454839 39454835 39454840 GAGAGAGAGGAGGGAGAGAGAGAAGAGAAGAGAGGAGAGGAGAGAGAGGAGGAAAGAGGAGAAGA GAGAGAGAGGAGGGAGAGAGAGAAGAGAA_____GAGAGGAGAGAGAGGAGGAAAGAGGAGAAGA AGAGAG A AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:39454817..39454882 26863196 MeRIP-seq:(Medium) rs570105068 Functional Loss DEL dbSNP153 30..34 33 - - - GWAS_ID_10070,GWAS_ID_10071,GWAS_ID_10072,GWAS_ID_10073,GWAS_ID_10074,GWAS_ID_10075 83145 RMVar_ID_83145 Human_SNP_ID_553394890 m1A Human chr14 + 44897464 44897464 44897464 GGGGAGGCCGAGACAGCCGGCGGTACTCATAGATGAGGCAGCGGCGGCGGCGGCGGCGGCGGCAG GGGGAGGCCGAGACAGCCGGCGGTACTCATAGGTGAGGCAGCGGCGGCGGCGGCGGCGGCGGCAG A G C14orf28 Ensembl:ENSG00000179476 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:44897272..44897640 26863196 MeRIP-seq:(Medium) rs1029817754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417952 83146 RMVar_ID_83146 Human_SNP_ID_553394925 m1A Human chr14 + 44897495 44897495 44897495 GATGAGGCAGCGGCGGCGGCGGCGGCGGCGGCAGCCCGGGCTCTCCATGAGCAGGCGGCGGCGGC GATGAGGCAGCGGCGGCGGCGGCGGCGGCGGCCGCCCGGGCTCTCCATGAGCAGGCGGCGGCGGC A C C14orf28 Ensembl:ENSG00000179476 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:44897393..44897543 26863410 MeRIP-seq:(Medium) rs1311807013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1510277,Human_Splice_Rec_1510285 83147 RMVar_ID_83147 Human_SNP_ID_553408094 m1A Human chr14 + 44942207 44942207 44942207 TCTGCATATATGAACCACCCATGTAATCATCTAATCAAAAGAACTCATTCATCTTGGATTCCTCC TCTGCATATATGAACCACCCATGTAATCATCTCATCAAAAGAACTCATTCATCTTGGATTCCTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:44942157..44942266 26863196 MeRIP-seq:(Medium) rs560737381 Functional Loss SNV dbSNP153 33..33 33 - - - 83148 RMVar_ID_83148 Human_SNP_ID_553408095 m1A Human chr14 + 44942207 44942207 44942207 TCTGCATATATGAACCACCCATGTAATCATCTAATCAAAAGAACTCATTCATCTTGGATTCCTCC TCTGCATATATGAACCACCCATGTAATCATCTTATCAAAAGAACTCATTCATCTTGGATTCCTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:44942157..44942266 26863196 MeRIP-seq:(Medium) rs560737381 Functional Loss SNV dbSNP153 33..33 33 - - - 83149 RMVar_ID_83149 Human_SNP_ID_230948751 m1A Human chr5 - 49659116 49659115 49659116 GGAATGGAAGGAATGGAATCAACGCGAGTGCAATGGAATGGAATGGAATGGAATGCAATGGAATG GGAATGGAAGGAATGGAATCAACGCGAGTGCAGGGGAATGGAATGGAATGGAATGCAATGGAATG AT CC - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:49658885..49659171 26863196 MeRIP-seq:(Medium) rs1554051820 Functional Loss MNV dbSNP153 33..34 33 - - - 83150 RMVar_ID_83150 Human_SNP_ID_230948752 m1A Human chr5 - 49659116 49659116 49659116 GGAATGGAAGGAATGGAATCAACGCGAGTGCAATGGAATGGAATGGAATGGAATGCAATGGAATG GGAATGGAAGGAATGGAATCAACGCGAGTGCAGTGGAATGGAATGGAATGGAATGCAATGGAATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:49658885..49659171 26863196 MeRIP-seq:(Medium) rs1297967348 Functional Loss SNV dbSNP153 33..33 33 - - - 83151 RMVar_ID_83151 Human_SNP_ID_230949045 m1A Human chr5 - 49660720 49660720 49660720 AATGGAAGGGAATGTAATCGAGTGGAATGGAAAGGAATAGAATCAACCCGAGTGGAATGGAAGGG AATGGAAGGGAATGTAATCGAGTGGAATGGAAGGGAATAGAATCAACCCGAGTGGAATGGAAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:49660566..49660856 26863196 MeRIP-seq:(Medium) rs1436447198 Functional Loss SNV dbSNP153 33..33 33 - - - 83152 RMVar_ID_83152 Human_SNP_ID_230949249 m1A Human chr5 - 49666487 49666486 49666488 GGAATGGAATGGAATGGAATGGAATGGAATGGAATCAAACCGAATGGAATGGAGTGGAATGGAAT GGAATGGAATGGAATGGAATGGAATGGAATGCCTTCAAACCGAATGGAATGGAGTGGAATGGAAT TTC AGG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:49666432..49666518 26863196 MeRIP-seq:(Medium) rs1554052038 Functional Loss MNV dbSNP153 32..34 33 - - - 83153 RMVar_ID_83153 Human_SNP_ID_231368197 m1A Human chr5 - 50666496 50666496 50666496 CGCGGGCTGCCGGGGCTCGCAGAGTATTAGCCATCCCGGGCGGGAGCCGCTTCTCCCCACACCGA CGCGGGCTGCCGGGGCTCGCAGAGTATTAGCCGTCCCGGGCGGGAGCCGCTTCTCCCCACACCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:50666447..50666663 26863196 MeRIP-seq:(Medium) rs1342323091 Functional Loss SNV dbSNP153 33..33 33 - - - 83154 RMVar_ID_83154 Human_SNP_ID_231392618 m1A Human chr5 + 50770686 50770682 50770686 AGAGGAAAGAAAGAAAAGAAAGAAATAACGAAAGAAAGCAAGCAAAGAAAGAAAGGAGAGAGAAA AGAGGAAAGAAAGAAAAGAAAGAAATAAC____GAAAGCAAGCAAAGAAAGAAAGGAGAGAGAAA CGAAA C PARP8 Ensembl:ENSG00000151883 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:50770526..50770709 26863196 MeRIP-seq:(Medium) rs1218123135 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_25899000 RMVar_hsa_circ_646,RMVar_hsa_circ_28233,RMVar_hsa_circ_361913,RMVar_hsa_circ_18393,RMVar_hsa_circ_67239,RMVar_hsa_circ_5494,RMVar_hsa_circ_338158,RMVar_hsa_circ_363381,RMVar_hsa_circ_313822,RMVar_hsa_circ_368169,RMVar_hsa_circ_303262,RMVar_hsa_circ_77145,RMVar_hsa_circ_231323,RMVar_hsa_circ_231324,RMVar_hsa_circ_231322,RMVar_hsa_circ_287509,RMVar_hsa_circ_307804,RMVar_hsa_circ_27500,RMVar_hsa_circ_231325,RMVar_hsa_circ_231327,RMVar_hsa_circ_5753,RMVar_hsa_circ_231326,RMVar_hsa_circ_56407,RMVar_hsa_circ_109310,RMVar_hsa_circ_359666,RMVar_hsa_circ_70549,RMVar_hsa_circ_231329,RMVar_hsa_circ_231330,RMVar_hsa_circ_111600 83155 RMVar_ID_83155 Human_SNP_ID_231920357 m1A Human chr5 + 52800200 52800200 52800200 GAGCCTGTTAGACGCAGCGCGCCGGGAGACTGAGAGAGGAAAGGATAGAGGAAGTGCTGCCCTAG GAGCCTGTTAGACGCAGCGCGCCGGGAGACTGCGAGAGGAAAGGATAGAGGAAGTGCTGCCCTAG A C PELO,ITGA1 Ensembl:ENSG00000152684,Ensembl:ENSG00000213949 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:52800149..52800390 26863196 MeRIP-seq:(Medium) rs566145776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4833263,Human_RBP_ID_5326771,Human_RBP_ID_18424950 83156 RMVar_ID_83156 Human_SNP_ID_231920363 m1A Human chr5 - 52800230 52800230 52800230 AGGAAACACGCTTGCTTCGACTCATGCAGCCTAGGGCAGCACTTCCTCTATCCTTTCCTCTCTCA AGGAAACACGCTTGCTTCGACTCATGCAGCCTTGGGCAGCACTTCCTCTATCCTTTCCTCTCTCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:52800182..52800372 26863196 MeRIP-seq:(Medium) rs1184969458 Functional Loss SNV dbSNP153 33..33 33 - - - 83157 RMVar_ID_83157 Human_SNP_ID_231920619 m1A Human chr5 + 52800878 52800878 52800878 TAGTCACTCCCAGCATGACCCTCACTCGGGCCAAGGTGGAGGTGAACATCCCTAGGAAAAGGAAA TAGTCACTCCCAGCATGACCCTCACTCGGGCCGAGGTGGAGGTGAACATCCCTAGGAAAAGGAAA A G PELO,ITGA1 Ensembl:ENSG00000152684,Ensembl:ENSG00000213949 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:52800651..52801059 32194978 MeRIP-seq:(Medium) rs753877060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041733,Human_RBP_ID_1655173 83158 RMVar_ID_83158 Human_SNP_ID_231928698 m1A Human chr5 + 52834599 52834593 52834599 AGAGAAGAAAGAAAGAAAGAGAGAGAGAGAAGAAAGAGAGAGAAAGAAGAAAGAAAGGGAGAGAA AGAGAAGAAAGAAAGAAAGAGAGAGAG______AAGAGAGAGAAAGAAGAAAGAAAGGGAGAGAA GAGAAGA G ITGA1 Ensembl:ENSG00000213949 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:52834563..52834656 26863196 MeRIP-seq:(Medium) rs1358149575 Functional Loss DEL dbSNP153 28..33 33 - - - 83159 RMVar_ID_83159 Human_SNP_ID_231939885 m1A Human chr5 - 52881994 52881994 52881994 TATACCTTGCTGTGTCTATTCCAAGAGCTGTCATAGTCTGGCGGCCACCTCTCTGGACTATTTTC TATACCTTGCTGTGTCTATTCCAAGAGCTGTCGTAGTCTGGCGGCCACCTCTCTGGACTATTTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:52881944..52882055 26863196 MeRIP-seq:(Medium) rs963575827 Functional Loss SNV dbSNP153 33..33 33 - - - 83160 RMVar_ID_83160 Human_SNP_ID_231946831 m1A Human chr5 + 52910407 52910407 52910407 ATTTATCATGGAAGTGGCAAGACTATAAGGAAAGAGTATGCACAAGTAAGAATTGAAACCTACAG ATTTATCATGGAAGTGGCAAGACTATAAGGAACGAGTATGCACAAGTAAGAATTGAAACCTACAG A C ITGA1 Ensembl:ENSG00000213949 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:52910383..52910496 26863196 MeRIP-seq:(Medium) rs1270124368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8237027 Human_Splice_Rec_649813,Human_Splice_Rec_649867,Human_Splice_Rec_649925 RMVar_hsa_circ_63668,RMVar_hsa_circ_71470,RMVar_hsa_circ_54200,RMVar_hsa_circ_66669,RMVar_hsa_circ_73082,RMVar_hsa_circ_118695,RMVar_hsa_circ_231342,RMVar_hsa_circ_41566,RMVar_hsa_circ_231341,RMVar_hsa_circ_52815,RMVar_hsa_circ_65879,RMVar_hsa_circ_96161 83161 RMVar_ID_83161 Human_SNP_ID_231946832 m1A Human chr5 + 52910407 52910407 52910407 ATTTATCATGGAAGTGGCAAGACTATAAGGAAAGAGTATGCACAAGTAAGAATTGAAACCTACAG ATTTATCATGGAAGTGGCAAGACTATAAGGAAGGAGTATGCACAAGTAAGAATTGAAACCTACAG A G ITGA1 Ensembl:ENSG00000213949 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:52910383..52910496 26863196 MeRIP-seq:(Medium) rs1270124368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8237027 Human_Splice_Rec_649813,Human_Splice_Rec_649867,Human_Splice_Rec_649925 RMVar_hsa_circ_63668,RMVar_hsa_circ_71470,RMVar_hsa_circ_54200,RMVar_hsa_circ_66669,RMVar_hsa_circ_73082,RMVar_hsa_circ_118695,RMVar_hsa_circ_231342,RMVar_hsa_circ_41566,RMVar_hsa_circ_231341,RMVar_hsa_circ_52815,RMVar_hsa_circ_65879,RMVar_hsa_circ_96161 83162 RMVar_ID_83162 Human_SNP_ID_231992994 m1A Human chr5 - 53098247 53098247 53098247 TGACTTTAACTAGCTCAGAAACGTACTCCCCCACCAACCCCACCTCACCGCCCCCCATCCCGGTT TGACTTTAACTAGCTCAGAAACGTACTCCCCCGCCAACCCCACCTCACCGCCCCCCATCCCGGTT T C MOCS2 Ensembl:ENSG00000164172 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:53098201..53098275 32194978 MeRIP-seq:(Medium) rs1009387229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_643162,Human_RBP_ID_7444566,Human_RBP_ID_9177586 83163 RMVar_ID_83163 Human_SNP_ID_232112570 m1A Human chr5 - 53560702 53560700 53560703 GGCAGCTACAGCCACTGCCCTTCTCCGCCACAACGTCTGCCTCAGTACCACTGACATTGACACCG GGCAGCTACAGCCACTGCCCTTCTCCGCCAC___GTCTGCCTCAGTACCACTGACATTGACACCG CGTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:53560651..53560775;chr5:53560651..53560796 26863196 MeRIP-seq:(Medium) rs1198698009 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18843540 83164 RMVar_ID_83164 Human_SNP_ID_232123460 m1A Human chr5 + 53603513 53603513 53603513 CACAGGACCAGACTCAAGACACACAACTCATAACAGTTGATGAAAAATTGGTAAGGATTTTCTAC CACAGGACCAGACTCAAGACACACAACTCATAGCAGTTGATGAAAAATTGGTAAGGATTTTCTAC A G NDUFS4 Ensembl:ENSG00000164258 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:53573724..53604736 32194978 MeRIP-seq:(Medium) rs756821245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041758,Human_RBP_ID_1655205,Human_RBP_ID_8617074,Human_RBP_ID_9399095,Human_RBP_ID_15457376,Human_RBP_ID_17301969,Human_RBP_ID_18049299 Human_Splice_Rec_650505,Human_Splice_Rec_650512,Human_Splice_Rec_650513,Human_Splice_Rec_650522,Human_Splice_Rec_650523,Human_Splice_Rec_650530,Human_Splice_Rec_650531,Human_Splice_Rec_650540,Human_Splice_Rec_650541 RMVar_hsa_circ_110132,RMVar_hsa_circ_231352,RMVar_hsa_circ_80678,RMVar_hsa_circ_90741,RMVar_hsa_circ_231353,RMVar_hsa_circ_334693,RMVar_hsa_circ_358771,RMVar_hsa_circ_370273,RMVar_hsa_circ_270015,RMVar_hsa_circ_231354,RMVar_hsa_circ_231356,RMVar_hsa_circ_231357,RMVar_hsa_circ_231358,RMVar_hsa_circ_231355 83165 RMVar_ID_83165 Human_SNP_ID_232143612 m1A Human chr5 - 53683242 53683242 53683242 TACTGCACAGCTGACTTTATTCACAGTCAAGCAGAGATATAGTCAGTGCCAACCTATTTTGTGGA TACTGCACAGCTGACTTTATTCACAGTCAAGCCGAGATATAGTCAGTGCCAACCTATTTTGTGGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:53683192..53683291 32194978 MeRIP-seq:(Medium) rs769636414 Functional Loss SNV dbSNP153 33..33 33 - - - 83166 RMVar_ID_83166 Human_SNP_ID_232295370 m1A Human chr5 - 54298549 54298549 54298549 AGAAGAGAAAGGGCTGGAACTGGAGGGGCAGGAAGGTTGGGGGGTGGCTTTCCTTAAATGGGACT AGAAGAGAAAGGGCTGGAACTGGAGGGGCAGGGAGGTTGGGGGGTGGCTTTCCTTAAATGGGACT T C ARL15 Ensembl:ENSG00000185305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:54298421..54298623 26863196 MeRIP-seq:(Medium) rs1424336698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24196,RMVar_hsa_circ_231372 83167 RMVar_ID_83167 Human_SNP_ID_232348910 m1A Human chr5 + 54517793 54517793 54517793 TCGGCGCTGCGAAGTGGAGGCGCTGCGAGCGGAGCCGCGCGGAGGGCGCGACCGGCTGGTCCGGG TCGGCGCTGCGAAGTGGAGGCGCTGCGAGCGGCGCCGCGCGGAGGGCGCGACCGGCTGGTCCGGG A C SNX18 Ensembl:ENSG00000178996 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:54517743..54517934 26863196 MeRIP-seq:(Medium) rs1352487169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845179 83168 RMVar_ID_83168 Human_SNP_ID_232348927 m1A Human chr5 - 54517820 54517820 54517820 AGCCCCGAAGGCGGCAAACCCACGCTGCCCGGACCAGCCGGTCGCGCCCTCCGCGCGGCTCCGCT AGCCCCGAAGGCGGCAAACCCACGCTGCCCGGCCCAGCCGGTCGCGCCCTCCGCGCGGCTCCGCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:54517770..54518001 26863196 MeRIP-seq:(Medium) rs1040186082 Functional Loss SNV dbSNP153 33..33 33 - - - 83169 RMVar_ID_83169 Human_SNP_ID_232349288 m1A Human chr5 + 54518428 54518426 54518429 AGGCAGCGATGATGACTGGGACGACGAGTGGGACGACAGCTCCACGGTGGCGGACGAGCCGGGCG AGGCAGCGATGATGACTGGGACGACGAGTGG___GACAGCTCCACGGTGGCGGACGAGCCGGGCG GGAC G SNX18 Ensembl:ENSG00000178996 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:54518205..54518454 26863196 MeRIP-seq:(Medium) rs1299922047 Functional Loss DEL dbSNP153 32..34 33 - - - 83170 RMVar_ID_83170 Human_SNP_ID_232349437 m1A Human chr5 - 54518703 54518703 54518703 CACCACGCACAGCTTGTCCCCGTCCTTCACGAAGCCTGACGCCTCCCCCAGCACGAAGGCCTCCC CACCACGCACAGCTTGTCCCCGTCCTTCACGACGCCTGACGCCTCCCCCAGCACGAAGGCCTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:54518652..54518752 26863196 MeRIP-seq:(Medium) rs1186518094 Functional Loss SNV dbSNP153 33..33 33 - - - 83171 RMVar_ID_83171 Human_SNP_ID_232349541 m1A Human chr5 - 54518899 54518899 54518899 ACTTCTCCGCCAGGCGCGCGTACAGCCAGTCGAAGTGCTTGTAGCGCCGATGCACCGGCACCTGC ACTTCTCCGCCAGGCGCGCGTACAGCCAGTCGTAGTGCTTGTAGCGCCGATGCACCGGCACCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:54518850..54518950 26863196 MeRIP-seq:(Medium) rs1168061518 Functional Loss SNV dbSNP153 33..33 33 - - - 83172 RMVar_ID_83172 Human_SNP_ID_232506851 m1A Human chr5 - 55166209 55166209 55166209 GCAGCTCCATTATCATCCATCTGGCAGTGGGGAGTCTCTGCTGCCCATGTGGTGCTGGCATATGC GCAGCTCCATTATCATCCATCTGGCAGTGGGGCGTCTCTGCTGCCCATGTGGTGCTGGCATATGC T G CDC20B Ensembl:ENSG00000164287 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:55166159..55166243 32194978 MeRIP-seq:(Medium) rs1048833946 Functional Loss SNV dbSNP153 33..33 33 - - - 83173 RMVar_ID_83173 Human_SNP_ID_232521979 m1A Human chr5 - 55226713 55226713 55226713 GCTCTGACGTCCTAGCTGCGAGCCTGGCGGAGAGGCTCAGGGCCCGCCCGGCGCGTGTCTCCCGG GCTCTGACGTCCTAGCTGCGAGCCTGGCGGAGGGGCTCAGGGCCCGCCCGGCGCGTGTCTCCCGG T C MCIDAS Ensembl:ENSG00000234602 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55226710..55226840 26863196 MeRIP-seq:(Medium) rs1437828233 Functional Loss SNV dbSNP153 33..33 33 - - - 83174 RMVar_ID_83174 Human_SNP_ID_232524035 m1A Human chr5 + 55233287 55233287 55233287 ACGGGCTGGGCCGGGCCGGGCAGGGGGCTACCACCCCGCGCCGCAGAGGGGCTCTCTGCGCCGTC ACGGGCTGGGCCGGGCCGGGCAGGGGGCTACCGCCCCGCGCCGCAGAGGGGCTCTCTGCGCCGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:55233239..55233436 32194978 MeRIP-seq:(Medium) rs1346814165 Functional Loss SNV dbSNP153 33..33 33 - - - 83175 RMVar_ID_83175 Human_SNP_ID_232541622 m1A Human chr5 - 55307464 55307464 55307464 ATCTGCCGAGGCTGGAATTGCCGGGGAGGCCCAAAGCAAGAAGCCAGTGTCCAGGCCGGCCACCG ATCTGCCGAGGCTGGAATTGCCGGGGAGGCCCGAAGCAAGAAGCCAGTGTCCAGGCCGGCCACCG T C DHX29 Ensembl:ENSG00000067248 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:55307418..55307654 26863196 MeRIP-seq:(Medium) rs1182757441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4833767,Human_RBP_ID_24108716 Human_Splice_Rec_651173,Human_Splice_Rec_651225,Human_Splice_Rec_651275,Human_Splice_Rec_651337 83176 RMVar_ID_83176 Human_SNP_ID_232541623 m1A Human chr5 - 55307464 55307464 55307464 ATCTGCCGAGGCTGGAATTGCCGGGGAGGCCCAAAGCAAGAAGCCAGTGTCCAGGCCGGCCACCG ATCTGCCGAGGCTGGAATTGCCGGGGAGGCCCCAAGCAAGAAGCCAGTGTCCAGGCCGGCCACCG T G DHX29 Ensembl:ENSG00000067248 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:55307418..55307654 26863196 MeRIP-seq:(Medium) rs1182757441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4833767,Human_RBP_ID_24108716 Human_Splice_Rec_651173,Human_Splice_Rec_651225,Human_Splice_Rec_651275,Human_Splice_Rec_651337 83177 RMVar_ID_83177 Human_SNP_ID_232541631 m1A Human chr5 + 55307484 55307484 55307484 GGCTTCTTGCTTTGGGCCTCCCCGGCAATTCCAGCCTCGGCAGATTTGGCTCTGGAAGCAGACAC GGCTTCTTGCTTTGGGCCTCCCCGGCAATTCCTGCCTCGGCAGATTTGGCTCTGGAAGCAGACAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:55307436..55307661 26863196 MeRIP-seq:(Medium) rs1394002901 Functional Loss SNV dbSNP153 33..33 33 - - - 83178 RMVar_ID_83178 Human_SNP_ID_232541710 m1A Human chr5 + 55307635 55307635 55307635 GCCCAGGCCCCGACGGTACCACTGCACAGCCGAGAGCTCTTCACATTCCCCGGCTCCGGGGCTGC GCCCAGGCCCCGACGGTACCACTGCACAGCCGGGAGCTCTTCACATTCCCCGGCTCCGGGGCTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:55307392..55307637 26863196 MeRIP-seq:(Medium) rs1158588394 Functional Loss SNV dbSNP153 33..33 33 - - - 83179 RMVar_ID_83179 Human_SNP_ID_232541813 m1A Human chr5 + 55307860 55307858 55307860 TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGG__AAAAAAAAAAAGTCAGGGGAACATTTTTGTCG GAA G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55307809..55307959 26863196 MeRIP-seq:(Medium) rs879182172 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 83180 RMVar_ID_83180 Human_SNP_ID_232541814 m1A Human chr5 + 55307860 55307858 55307860 TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGA_AAAAAAAAAAAGTCAGGGGAACATTTTTGTCG GAA GA NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55307809..55307959 26863196 MeRIP-seq:(Medium) rs879182172 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 83181 RMVar_ID_83181 Human_SNP_ID_232541818 m1A Human chr5 + 55307860 55307860 55307860 TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAGAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG A G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55307809..55307959 26863196 MeRIP-seq:(Medium) rs74556806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 83182 RMVar_ID_83182 Human_SNP_ID_232541819 m1A Human chr5 + 55307862 55307862 55307862 GGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCGGC GGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAGAAAAAAAAAGTCAGGGGAACATTTTTGTCGGC A G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:55307812..55307922 26863196 MeRIP-seq:(Medium) rs1411819171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 83183 RMVar_ID_83183 Human_SNP_ID_232541926 m1A Human chr5 - 55308050 55308050 55308050 GGTTCCCGCCGCAGTGGTCGAGTCGCCCTCGAACACGCTGAACAGCTCATCTCCGAATGCGTCCG GGTTCCCGCCGCAGTGGTCGAGTCGCCCTCGAGCACGCTGAACAGCTCATCTCCGAATGCGTCCG T C lnc-DHX29-1 RNACentral:URS00008BA384 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:55308001..55308150 26863196 MeRIP-seq:(Medium) rs762480114 Functional Loss SNV dbSNP153 33..33 33 - - - 83184 RMVar_ID_83184 Human_SNP_ID_232541963 m1A Human chr5 + 55308111 55308111 55308111 AACCAAAAAAGACAAGGAAAAGGACAAGGGGAAATGGAAGGGGCCTCCAGGGTCTGCAGACAAGG AACCAAAAAAGACAAGGAAAAGGACAAGGGGATATGGAAGGGGCCTCCAGGGTCTGCAGACAAGG A T MTREX Ensembl:ENSG00000039123 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55308001..55322387 26863196 MeRIP-seq:(Medium) rs913671595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838391,Human_RBP_ID_4855715,Human_RBP_ID_7446836,Human_RBP_ID_9177757,Human_RBP_ID_26350832,Human_RBP_ID_27825389 Human_Splice_Rec_651343,Human_Splice_Rec_651395,Human_Splice_Rec_651401,Human_Splice_Rec_651449,Human_Splice_Rec_651459 RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 83185 RMVar_ID_83185 Human_SNP_ID_232547152 m1A Human chr5 + 55328751 55328751 55328751 TGCTTTTCAAAGAGAGGCCATTCAGTGTGTTGACAATAATCAGTCTGTTCTAGTATCTGCACATA TGCTTTTCAAAGAGAGGCCATTCAGTGTGTTGTCAATAATCAGTCTGTTCTAGTATCTGCACATA A T MTREX Ensembl:ENSG00000039123 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:55327744..55328765 32194978 MeRIP-seq:(Medium) rs763547460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73458,Human_RBP_ID_15461461,Human_RBP_ID_18843833,Human_RBP_ID_22460049,Human_RBP_ID_26826273 Human_Splice_Rec_651350,Human_Splice_Rec_651351,Human_Splice_Rec_651404,Human_Splice_Rec_651405,Human_Splice_Rec_651456,Human_Splice_Rec_651457 Human_miRNA_ID_2761407 RMVar_hsa_circ_5210,RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394,RMVar_hsa_circ_57533,RMVar_hsa_circ_317315,RMVar_hsa_circ_346224,RMVar_hsa_circ_338462,RMVar_hsa_circ_313020,RMVar_hsa_circ_41521,RMVar_hsa_circ_21872,RMVar_hsa_circ_15159,RMVar_hsa_circ_231402,RMVar_hsa_circ_44573,RMVar_hsa_circ_231396,RMVar_hsa_circ_231398,RMVar_hsa_circ_231399,RMVar_hsa_circ_231400,RMVar_hsa_circ_231397,RMVar_hsa_circ_277166,RMVar_hsa_circ_344914,RMVar_hsa_circ_376279,RMVar_hsa_circ_333399,RMVar_hsa_circ_45085,RMVar_hsa_circ_10290,RMVar_hsa_circ_34579,RMVar_hsa_circ_231404,RMVar_hsa_circ_231405,RMVar_hsa_circ_231403,RMVar_hsa_circ_297942,RMVar_hsa_circ_306042,RMVar_hsa_circ_315937,RMVar_hsa_circ_231401,RMVar_hsa_circ_322119,RMVar_hsa_circ_314480,RMVar_hsa_circ_302012,RMVar_hsa_circ_303907,RMVar_hsa_circ_301475,RMVar_hsa_circ_58089,RMVar_hsa_circ_275261,RMVar_hsa_circ_16682,RMVar_hsa_circ_231407,RMVar_hsa_circ_231409,RMVar_hsa_circ_231411,RMVar_hsa_circ_231413,RMVar_hsa_circ_8526,RMVar_hsa_circ_231412,RMVar_hsa_circ_231410,RMVar_hsa_circ_231408,RMVar_hsa_circ_9286,RMVar_hsa_circ_231406,RMVar_hsa_circ_319579 83186 RMVar_ID_83186 Human_SNP_ID_232561248 m1A Human chr5 + 55387988 55387988 55387988 TTCTGTTTTGTTTTTTAGCCTAACTCTGGTGAACTGGATCCTTTGTATGTAGTAGAAGTACTTCT TTCTGTTTTGTTTTTTAGCCTAACTCTGGTGACCTGGATCCTTTGTATGTAGTAGAAGTACTTCT A C MTREX Ensembl:ENSG00000039123 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:55387981..55397445 32194978 MeRIP-seq:(Medium) rs754780180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942805,Human_RBP_ID_3967207,Human_RBP_ID_15462460,Human_RBP_ID_22460057,Human_RBP_ID_22553269,Human_RBP_ID_22771356 Human_Splice_Rec_651378,Human_Splice_Rec_651432 Human_miRNA_ID_2802728,Human_miRNA_ID_2837569,Human_miRNA_ID_2855448 RMVar_hsa_circ_41521,RMVar_hsa_circ_1857,RMVar_hsa_circ_60701,RMVar_hsa_circ_44573,RMVar_hsa_circ_344914,RMVar_hsa_circ_45085,RMVar_hsa_circ_231401,RMVar_hsa_circ_301475,RMVar_hsa_circ_16682,RMVar_hsa_circ_302006,RMVar_hsa_circ_231411,RMVar_hsa_circ_231413,RMVar_hsa_circ_8526,RMVar_hsa_circ_231412,RMVar_hsa_circ_319579,RMVar_hsa_circ_366330,RMVar_hsa_circ_324693,RMVar_hsa_circ_231415,RMVar_hsa_circ_231426,RMVar_hsa_circ_27044,RMVar_hsa_circ_286698,RMVar_hsa_circ_126461,RMVar_hsa_circ_231427,RMVar_hsa_circ_118109,RMVar_hsa_circ_123632,RMVar_hsa_circ_231434,RMVar_hsa_circ_55082,RMVar_hsa_circ_231435,RMVar_hsa_circ_70684,RMVar_hsa_circ_107960,RMVar_hsa_circ_231438,RMVar_hsa_circ_60619,RMVar_hsa_circ_37695,RMVar_hsa_circ_351013,RMVar_hsa_circ_67412,RMVar_hsa_circ_66522,RMVar_hsa_circ_363339,RMVar_hsa_circ_72735,RMVar_hsa_circ_58113,RMVar_hsa_circ_231442 83187 RMVar_ID_83187 Human_SNP_ID_232597320 m1A Human chr5 + 55534834 55534833 55534835 GCCAGCAATGGCGCCCGGGGCCCTCCCCTCACAGCCCCCGCGAACACTCGGTTAGTGCCGAGGCG GCCAGCAATGGCGCCCGGGGCCCTCCCCTCAC__CCCCCGCGAACACTCGGTTAGTGCCGAGGCG CAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55534783..55535015 26863196 MeRIP-seq:(Medium) rs1279853642 Functional Loss DEL dbSNP153 33..34 33 - - - 83188 RMVar_ID_83188 Human_SNP_ID_232597350 m1A Human chr5 - 55534936 55534936 55534936 CTGTGGGAGAGAGCGCCGGGATCCGGACGGGGAGCAACCGGGGCAGGCCGTGCCGGCTGAGGAGG CTGTGGGAGAGAGCGCCGGGATCCGGACGGGGGGCAACCGGGGCAGGCCGTGCCGGCTGAGGAGG T C PLPP1 Ensembl:ENSG00000067113 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:55534886..55534974 26863196 MeRIP-seq:(Medium) rs1173580625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845182 Human_miRNA_ID_2150832,Human_miRNA_ID_2419320 RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 83189 RMVar_ID_83189 Human_SNP_ID_232607398 m1A Human chr5 + 55575575 55575574 55575575 CTACACAAGTGATAATATTGTGTAAATACACCACCGCCCCCCCACCCCACCCCCCCCCCCCCGCC CTACACAAGTGATAATATTGTGTAAATACACC_CCGCCCCCCCACCCCACCCCCCCCCCCCCGCC CA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:55575569..55575696 26863196 MeRIP-seq:(Medium) rs1288690620 Functional Loss DEL dbSNP153 33..33 33 - - - 83190 RMVar_ID_83190 Human_SNP_ID_232607400 m1A Human chr5 + 55575575 55575575 55575575 CTACACAAGTGATAATATTGTGTAAATACACCACCGCCCCCCCACCCCACCCCCCCCCCCCCGCC CTACACAAGTGATAATATTGTGTAAATACACCCCCGCCCCCCCACCCCACCCCCCCCCCCCCGCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:55575569..55575696 26863196 MeRIP-seq:(Medium) rs1270787541 Functional Loss SNV dbSNP153 33..33 33 - - - 83191 RMVar_ID_83191 Human_SNP_ID_232708259 m1A Human chr5 + 55994912 55994911 55994913 CCGGTTCAGCTGCGCCGGGGCGGCCCAGCGCGACTCCGCGGGCCTTTTGGCTGCTCGCCCCGGCT CCGGTTCAGCTGCGCCGGGGCGGCCCAGCGCG__TCCGCGGGCCTTTTGGCTGCTCGCCCCGGCT GAC G AC008892.1 Ensembl:ENSG00000249236 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55994776..55994975 26863196 MeRIP-seq:(Medium) rs1404841947 Functional Loss DEL dbSNP153 33..34 33 - - - 83192 RMVar_ID_83192 Human_SNP_ID_232909162 m1A Human chr5 - 56815604 56815604 56815604 GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGACGAGGCGCGATTCCCCGCCGCCGCCGCCATTT GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGTCGAGGCGCGATTCCCCGCCGCCGCCGCCATTT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:56815573..56815731 26863196 MeRIP-seq:(Medium) rs891002481 Functional Loss SNV dbSNP153 33..33 33 - - - 83193 RMVar_ID_83193 Human_SNP_ID_232909163 m1A Human chr5 - 56815604 56815604 56815604 GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGACGAGGCGCGATTCCCCGCCGCCGCCGCCATTT GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGGCGAGGCGCGATTCCCCGCCGCCGCCGCCATTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:56815573..56815731 26863196 MeRIP-seq:(Medium) rs891002481 Functional Loss SNV dbSNP153 33..33 33 - - - 83194 RMVar_ID_83194 Human_SNP_ID_232909164 m1A Human chr5 - 56815604 56815604 56815604 GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGACGAGGCGCGATTCCCCGCCGCCGCCGCCATTT GCTCGTAGCCCTGGCGCCCGGGAATCCCGACGCCGAGGCGCGATTCCCCGCCGCCGCCGCCATTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:56815573..56815731 26863196 MeRIP-seq:(Medium) rs891002481 Functional Loss SNV dbSNP153 33..33 33 - - - 83195 RMVar_ID_83195 Human_SNP_ID_232909644 m1A Human chr5 + 56816448 56816448 56816448 CGGCGGCGCCCCCGGACGGGTGTCCCCGGGGCAAAGGCACTGGGGGGCGAGGCCCGAGCCTGAGG CGGCGGCGCCCCCGGACGGGTGTCCCCGGGGCGAAGGCACTGGGGGGCGAGGCCCGAGCCTGAGG A G MAP3K1 Ensembl:ENSG00000095015 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:56816442..56816634 26863196 MeRIP-seq:(Medium) rs1172610411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845187,Human_RBP_ID_8213957,Human_RBP_ID_9436529 RMVar_hsa_circ_110791,RMVar_hsa_circ_231502 83196 RMVar_ID_83196 Human_SNP_ID_232920093 m1A Human chr5 + 56856663 56856663 56856663 GGGTTGCACAAGATGGATGATCGTCCAGAGGAACGAATGATCAGGGAGAAACTGAAGGCAACCTG GGGTTGCACAAGATGGATGATCGTCCAGAGGAGCGAATGATCAGGGAGAAACTGAAGGCAACCTG A G MAP3K1 Ensembl:ENSG00000095015 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:56856571..56856696 26863196 MeRIP-seq:(Medium) rs766636754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1996551 Human_Splice_Rec_652876,Human_Splice_Rec_652877 Human_miRNA_ID_121529,Human_miRNA_ID_125346,Human_miRNA_ID_1268252,Human_miRNA_ID_2010781,Human_miRNA_ID_2564785,Human_miRNA_ID_3000835 RMVar_hsa_circ_7858,RMVar_hsa_circ_78671,RMVar_hsa_circ_311009,RMVar_hsa_circ_110791,RMVar_hsa_circ_231502,RMVar_hsa_circ_322466,RMVar_hsa_circ_293008,RMVar_hsa_circ_303674,RMVar_hsa_circ_103915,RMVar_hsa_circ_58974,RMVar_hsa_circ_74929,RMVar_hsa_circ_15287,RMVar_hsa_circ_231505,RMVar_hsa_circ_231507,RMVar_hsa_circ_231508,RMVar_hsa_circ_231509,RMVar_hsa_circ_231506,RMVar_hsa_circ_231503,RMVar_hsa_circ_231504 83197 RMVar_ID_83197 Human_SNP_ID_232943952 m1A Human chr5 - 56952057 56952057 56952057 GCAGGGAAACCGGGCAGGAGCAGCCGGGCTGGAGCGGGCGCCCGGCGGCTCCCCGCGACCCCCGA GCAGGGAAACCGGGCAGGAGCAGCCGGGCTGGCGCGGGCGCCCGGCGGCTCCCCGCGACCCCCGA T G MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:56951763..56952083 26863196 MeRIP-seq:(Medium) rs1326152850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788179,Human_RBP_ID_944259,Human_RBP_ID_5397245,Human_RBP_ID_8213149,Human_RBP_ID_19124442,Human_RBP_ID_26792067 RMVar_hsa_circ_231527,RMVar_hsa_circ_87425 83198 RMVar_ID_83198 Human_SNP_ID_232944173 m1A Human chr5 + 56952528 56952528 56952528 CCGCGGCGCGGGAGGGCGTGCGGGAGGCGGGCAGGAGACTTGGACTGGCAGGCGATGTGCAGGGG CCGCGGCGCGGGAGGGCGTGCGGGAGGCGGGCGGGAGACTTGGACTGGCAGGCGATGTGCAGGGG A G lnc-SETD9-5,lnc-SETD9-5:2 RNACentral:URS0000D5A98E,RNACentral:URS0000D5CFFB lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:56952456..56952584 26863196 MeRIP-seq:(Medium) rs1204280063 Functional Loss SNV dbSNP153 33..33 33 - - - 83199 RMVar_ID_83199 Human_SNP_ID_233000188 m1A Human chr5 + 57174121 57174121 57174121 CTGAGACTGGTTGTGGGGGAGGGAAAAGCGGCAAAAGGGGATTATTCAAAGTACCGAAAACCTTC CTGAGACTGGTTGTGGGGGAGGGAAAAGCGGCCAAAGGGGATTATTCAAAGTACCGAAAACCTTC A C GPBP1 Ensembl:ENSG00000062194 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:57174054..57174178 26863196 MeRIP-seq:(Medium) rs1167748641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845712,Human_RBP_ID_9177965,Human_RBP_ID_18424953,Human_RBP_ID_26350842 Human_Splice_Rec_653149,Human_Splice_Rec_653171,Human_Splice_Rec_653189 RMVar_hsa_circ_231529,RMVar_hsa_circ_109415 83200 RMVar_ID_83200 Human_SNP_ID_233000212 m1A Human chr5 - 57174196 57174196 57174196 CTAGAGGACGGTGTTACCTTCTGCCCCACCAGAGGTGCCCCTGGCCTGGGGGTGCCGCCGCGCCT CTAGAGGACGGTGTTACCTTCTGCCCCACCAGGGGTGCCCCTGGCCTGGGGGTGCCGCCGCGCCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:57174146..57175582 32194978 MeRIP-seq:(Medium) rs763624942 Functional Loss SNV dbSNP153 33..33 33 - - - 83201 RMVar_ID_83201 Human_SNP_ID_233000241 m1A Human chr5 - 57174267 57174267 57174267 CCGCTCCCGACCCCTCAAACCCCAACACGGACACGGGCACTCCCCTCCTCCCCCGGGCTCGGGCG CCGCTCCCGACCCCTCAAACCCCAACACGGACGCGGGCACTCCCCTCCTCCCCCGGGCTCGGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:57174248..57174414 26863196 MeRIP-seq:(Medium) rs1373980656 Functional Loss SNV dbSNP153 33..33 33 - - - 83202 RMVar_ID_83202 Human_SNP_ID_233025921 m1A Human chr5 - 57262838 57262833 57262838 AATCCTCTTCTAATGGGGTATTTCACTACATAAATTATAGTTCTTCATTTTTACAATTCACCCCA AATCCTCTTCTAATGGGGTATTTCACTACATA_____TAGTTCTTCATTTTTACAATTCACCCCA ATAATT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:57262737..57262837 32194978 MeRIP-seq:(Medium) rs1300323733 Functional Loss DEL dbSNP153 33..37 33 - - - 83203 RMVar_ID_83203 Human_SNP_ID_233025922 m1A Human chr5 - 57262838 57262838 57262838 AATCCTCTTCTAATGGGGTATTTCACTACATAAATTATAGTTCTTCATTTTTACAATTCACCCCA AATCCTCTTCTAATGGGGTATTTCACTACATATATTATAGTTCTTCATTTTTACAATTCACCCCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:57262737..57262837 32194978 MeRIP-seq:(Medium) rs1022497260 Functional Loss SNV dbSNP153 33..33 33 - - - 83204 RMVar_ID_83204 Human_SNP_ID_233319860 m1A Human chr5 - 58455683 58455683 58455683 GGAAAACATGCCGGAAGCTGATTGCATTCCCAAAGAGCAGCTGAGCACATCATTTCAGTGGGTCA GGAAAACATGCCGGAAGCTGATTGCATTCCCAGAGAGCAGCTGAGCACATCATTTCAGTGGGTCA T C PLK2 Ensembl:ENSG00000145632 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:58455601..58456195 32194978 MeRIP-seq:(Medium) rs1460916591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75633 Human_Splice_Rec_653402,Human_Splice_Rec_653436,Human_Splice_Rec_653446,Human_Splice_Rec_653452 RMVar_hsa_circ_30401,RMVar_hsa_circ_231552,RMVar_hsa_circ_121211,RMVar_hsa_circ_231553,RMVar_hsa_circ_78038,RMVar_hsa_circ_89591,RMVar_hsa_circ_231554,RMVar_hsa_circ_231555 83205 RMVar_ID_83205 Human_SNP_ID_233320681 m1A Human chr5 - 58458484 58458484 58458484 ATTTTGAAAGCAAGAAAGGTGTTGACAGAGCCAGAAGTTCGATACTACCTCAGGCAGATTGTGTC ATTTTGAAAGCAAGAAAGGTGTTGACAGAGCCGGAAGTTCGATACTACCTCAGGCAGATTGTGTC T C PLK2 Ensembl:ENSG00000145632 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:58458436..58458537 32194978 MeRIP-seq:(Medium) rs1392004258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75637 Human_Splice_Rec_653388,Human_Splice_Rec_653389,Human_Splice_Rec_653422,Human_Splice_Rec_653423,Human_Splice_Rec_653466,Human_Splice_Rec_653474,Human_Splice_Rec_653475,Human_Splice_Rec_653486,Human_Splice_Rec_653487 Human_miRNA_ID_795205,Human_miRNA_ID_1307027,Human_miRNA_ID_1913687,Human_miRNA_ID_1916139,Human_miRNA_ID_1918587,Human_miRNA_ID_1921044,Human_miRNA_ID_1923501,Human_miRNA_ID_1925952,Human_miRNA_ID_1928402,Human_miRNA_ID_1930855,Human_miRNA_ID_2082709,Human_miRNA_ID_2167960,Human_miRNA_ID_2169484,Human_miRNA_ID_3068332,Human_miRNA_ID_3124536 RMVar_hsa_circ_231553,RMVar_hsa_circ_89591,RMVar_hsa_circ_84357,RMVar_hsa_circ_93590,RMVar_hsa_circ_231560,RMVar_hsa_circ_55394,RMVar_hsa_circ_231561 83206 RMVar_ID_83206 Human_SNP_ID_233321196 m1A Human chr5 + 58460009 58460007 58460009 GCACTGCCCGCTGCCACCCCCTAGGCGCGGTCACACGTCCGAGCCGGCCGTGGTCCTCGCACCCT GCACTGCCCGCTGCCACCCCCTAGGCGCGGT__CACGTCCGAGCCGGCCGTGGTCCTCGCACCCT TCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:58459961..58460032 26863196 MeRIP-seq:(Medium) rs1324865459 Functional Loss DEL dbSNP153 32..33 33 - - - 83207 RMVar_ID_83207 Human_SNP_ID_233321204 m1A Human chr5 - 58460027 58460027 58460027 TAGTCGGCACCAGAGGCAAGGGTGCGAGGACCACGGCCGGCTCGGACGTGTGACCGCGCCTAGGG TAGTCGGCACCAGAGGCAAGGGTGCGAGGACCTCGGCCGGCTCGGACGTGTGACCGCGCCTAGGG T A PLK2 Ensembl:ENSG00000145632 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:58459726..58460100;chr5:58459676..58460100 26863196 MeRIP-seq:(Medium) rs974221193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788738 83208 RMVar_ID_83208 Human_SNP_ID_233458962 m1A Human chr5 + 59019559 59019559 59019559 TCCTCTGTTCCAGAGAGGCTCACTCCTCCAGAATGCCCACTACCCTCCTCTCCAGCAAACATACA TCCTCTGTTCCAGAGAGGCTCACTCCTCCAGATTGCCCACTACCCTCCTCTCCAGCAAACATACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59019509..59019695 26863196 MeRIP-seq:(Medium) rs1175589486 Functional Loss SNV dbSNP153 33..33 33 - - - 83209 RMVar_ID_83209 Human_SNP_ID_233459596 m1A Human chr5 + 59022349 59022349 59022349 CTCCTTCTCCCACTCTTCTCTTTCTCTGCCTCACACTGCCTAATACGTCTTTCCTCTTTCTCTCT CTCCTTCTCCCACTCTTCTCTTTCTCTGCCTCCCACTGCCTAATACGTCTTTCCTCTTTCTCTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59022298..59022635 26863196 MeRIP-seq:(Medium) rs1000308274 Functional Loss SNV dbSNP153 33..33 33 - - - 83210 RMVar_ID_83210 Human_SNP_ID_233459642 m1A Human chr5 + 59022534 59022534 59022534 GAACCTGCTTACACCTTCCGTGAGTTTATCCTATATCTTCTCTATCTGCTGTCTGCTTCCCACTA GAACCTGCTTACACCTTCCGTGAGTTTATCCTGTATCTTCTCTATCTGCTGTCTGCTTCCCACTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:59022485..59022636 26863196 MeRIP-seq:(Medium) rs950025310 Functional Loss SNV dbSNP153 33..33 33 - - - 83211 RMVar_ID_83211 Human_SNP_ID_233463871 m1A Human chr5 + 59039478 59039478 59039478 CCTGCCGAGCCTTCTGCACGGCACTTGAAGTGAATGAATCAGCCGCGGCCGGGTGCGCGGCCACC CCTGCCGAGCCTTCTGCACGGCACTTGAAGTGGATGAATCAGCCGCGGCCGGGTGCGCGGCCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:59039458..59039584;chr5:59039441..59039592 26863196 MeRIP-seq:(Medium) rs1254963474 Functional Loss SNV dbSNP153 33..33 33 - - - 83212 RMVar_ID_83212 Human_SNP_ID_233474454 m1A Human chr5 - 59086452 59086452 59086452 ACAAAGAGATTGAGAAGTAGTGGCTGAGAAGTAGGCAGAAATTTAGGAGAGTGGTGTTCTCAACT ACAAAGAGATTGAGAAGTAGTGGCTGAGAAGTGGGCAGAAATTTAGGAGAGTGGTGTTCTCAACT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59086438..59086593 26863196 MeRIP-seq:(Medium) rs1286564512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324536,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202 83213 RMVar_ID_83213 Human_SNP_ID_233474793 m1A Human chr5 - 59087801 59087801 59087801 TAGAAAGGAAAGATGAGTAAGGTTGGGGGTCAATAGTTCGAGCAAATATTGCAGTATGAAAGGTG TAGAAAGGAAAGATGAGTAAGGTTGGGGGTCAGTAGTTCGAGCAAATATTGCAGTATGAAAGGTG T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59087793..59087865 26863196 MeRIP-seq:(Medium) rs957163443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324536,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202 83214 RMVar_ID_83214 Human_SNP_ID_233486755 m1A Human chr5 - 59139074 59139074 59139074 TAGCCTGCAGTGTATAGTTTCCTGATCAAGCCAAGCTCTCCCACACCTCTGTAACTTTTGCGTAT TAGCCTGCAGTGTATAGTTTCCTGATCAAGCCGAGCTCTCCCACACCTCTGTAACTTTTGCGTAT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:59139026..59139100 26863196 MeRIP-seq:(Medium) rs1488094813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21089106 RMVar_hsa_circ_324536,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 83215 RMVar_ID_83215 Human_SNP_ID_233492993 m1A Human chr5 + 59164801 59164801 59164801 AAACGTTGGGTAAGGAAGGCATGATTGCACCCAGGCGAAGTGAATGGCTACGCAGAGGGCACAGA AAACGTTGGGTAAGGAAGGCATGATTGCACCCCGGCGAAGTGAATGGCTACGCAGAGGGCACAGA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:59164751..59164950 26863196 MeRIP-seq:(Medium) rs1408410751 Functional Loss SNV dbSNP153 33..33 33 - - - 83216 RMVar_ID_83216 Human_SNP_ID_233520062 m1A Human chr5 + 59275867 59275867 59275867 GAGGTACTGTAACACGGGAGAGCTGTCAAGGAAGTTCCATTTCAGGGCAAGCACAGGAAAACACT GAGGTACTGTAACACGGGAGAGCTGTCAAGGATGTTCCATTTCAGGGCAAGCACAGGAAAACACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59275865..59275984 26863196 MeRIP-seq:(Medium) rs1416720193 Functional Loss SNV dbSNP153 33..33 33 - - - 83217 RMVar_ID_83217 Human_SNP_ID_233531546 m1A Human chr5 - 59324037 59324037 59324037 GTGGAAGGAGAGAGAGGGTATCAGGTAGACACAGTATCATGTGCAAATGACTGGGAATAAGATAA GTGGAAGGAGAGAGAGGGTATCAGGTAGACACGGTATCATGTGCAAATGACTGGGAATAAGATAA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:59323923..59324090 26863196 MeRIP-seq:(Medium) rs1009514294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973 83218 RMVar_ID_83218 Human_SNP_ID_233534270 m1A Human chr5 + 59334974 59334974 59334974 GCCTCTGCTTTTCACTTGGCTAATTCCTATTCACTCCTCATTTTTCAGCTTATACACTACTTCCT GCCTCTGCTTTTCACTTGGCTAATTCCTATTCCCTCCTCATTTTTCAGCTTATACACTACTTCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:59334945..59335041 26863196 MeRIP-seq:(Medium) rs1051246250 Functional Loss SNV dbSNP153 33..33 33 - - - 83219 RMVar_ID_83219 Human_SNP_ID_233534274 m1A Human chr5 - 59334986 59334986 59334986 AAGGCTGCTGGAAGGAAGTAGTGTATAAGCTGAAAAATGAGGAGTGAATAGGAATTAGCCAAGTG AAGGCTGCTGGAAGGAAGTAGTGTATAAGCTGGAAAATGAGGAGTGAATAGGAATTAGCCAAGTG T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59334937..59335029 26863196 MeRIP-seq:(Medium) rs919729009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973 83220 RMVar_ID_83220 Human_SNP_ID_233578510 m1A Human chr5 - 59519103 59519101 59519103 GGGAAGAGGAGGAAGGAGGGAGAGAGAGAAAGAGGAAAGTTGAAAGAAGAAAGGAAGGGAAGAAA GGGAAGAGGAGGAAGGAGGGAGAGAGAGAAAG__GAAAGTTGAAAGAAGAAAGGAAGGGAAGAAA CCT C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:59519052..59519197 26863196 MeRIP-seq:(Medium) rs1437851190 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25942356 RMVar_hsa_circ_25249,RMVar_hsa_circ_231592,RMVar_hsa_circ_231594,RMVar_hsa_circ_231593,RMVar_hsa_circ_231595 83221 RMVar_ID_83221 Human_SNP_ID_233602561 m1A Human chr5 - 59620509 59620509 59620509 TTCACCTCCATGGCCACACTCTGAACTTTGTCATCAGCCAGAACTGCTCCAACCAACCTCAAAAT TTCACCTCCATGGCCACACTCTGAACTTTGTCGTCAGCCAGAACTGCTCCAACCAACCTCAAAAT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:59620417..59620573 26863196 MeRIP-seq:(Medium) rs1045338582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8618466,Human_RBP_ID_10211998,Human_RBP_ID_21089605,Human_RBP_ID_23243607 RMVar_hsa_circ_25249 83222 RMVar_ID_83222 Human_SNP_ID_233632417 m1A Human chr5 - 59746728 59746727 59746728 GGGCAGCCAGTAGTGTCAGAGCAAGATGGTGCAGGAAAGTCAGAGAACATGCTGAAGATACAGGA GGGCAGCCAGTAGTGTCAGAGCAAGATGGTGC_GGAAAGTCAGAGAACATGCTGAAGATACAGGA CT C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:59746677..59746754 26863196 MeRIP-seq:(Medium) rs1337554127 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 83223 RMVar_ID_83223 Human_SNP_ID_158129955 m1A Human chr3 - 150408401 150408401 150408401 AACCCCGAAGAAACTGAAATTCAAACTGCTGAAGCGGCGGCTGCAGCTCCCTCCGCTGGGCCAAG AACCCCGAAGAAACTGAAATTCAAACTGCTGAGGCGGCGGCTGCAGCTCCCTCCGCTGGGCCAAG T C lnc-SERP1-4,lnc-SERP1-4:2,lnc-SERP1-4:3,lnc-SERP1-4:4 RNACentral:URS0000D5D051,RNACentral:URS00009B434B,RNACentral:URS0000D5802F,RNACentral:URS0000D5885C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:150408350..150408574 26863196 MeRIP-seq:(Medium) rs1202989606 Functional Loss SNV dbSNP153 33..33 33 - - - 83224 RMVar_ID_83224 Human_SNP_ID_158129956 m1A Human chr3 - 150408401 150408401 150408401 AACCCCGAAGAAACTGAAATTCAAACTGCTGAAGCGGCGGCTGCAGCTCCCTCCGCTGGGCCAAG AACCCCGAAGAAACTGAAATTCAAACTGCTGACGCGGCGGCTGCAGCTCCCTCCGCTGGGCCAAG T G lnc-SERP1-4,lnc-SERP1-4:2,lnc-SERP1-4:3,lnc-SERP1-4:4 RNACentral:URS0000D5D051,RNACentral:URS00009B434B,RNACentral:URS0000D5802F,RNACentral:URS0000D5885C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:150408350..150408574 26863196 MeRIP-seq:(Medium) rs1202989606 Functional Loss SNV dbSNP153 33..33 33 - - - 83225 RMVar_ID_83225 Human_SNP_ID_158129977 m1A Human chr3 + 150408485 150408483 150408485 GGAGGAGCCGGAGAAGCCACCACCGCTACCTCACACAGCCGGGGCGCCTCCGGTCCCGTGCCAGC GGAGGAGCCGGAGAAGCCACCACCGCTACCT__CACAGCCGGGGCGCCTCCGGTCCCGTGCCAGC TCA T TSC22D2 Ensembl:ENSG00000196428 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:150408434..150408535 26863196 MeRIP-seq:(Medium) rs1179910278 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_248660,Human_RBP_ID_4727022,Human_RBP_ID_5505675,Human_RBP_ID_22092521 83226 RMVar_ID_83226 Human_SNP_ID_158130083 m1A Human chr3 + 150408736 150408736 150408736 GAGGGAGGGCCGCCTGCCCGCGCCACAGCCCCACCGCCCGCCCGCGGACCTTCAGCCAGCTCCGG GAGGGAGGGCCGCCTGCCCGCGCCACAGCCCCTCCGCCCGCCCGCGGACCTTCAGCCAGCTCCGG A T TSC22D2 Ensembl:ENSG00000196428 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:150408689..150409212 26863196 MeRIP-seq:(Medium) rs1413262870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5325700 83227 RMVar_ID_83227 Human_SNP_ID_158130235 m1A Human chr3 + 150409127 150409127 150409127 AAAAAGGAAGGAGGAGCCGCCGCGGGACTGAGACGGGGGCAGAGCCGAAGAGACCGACACAGAGA AAAAAGGAAGGAGGAGCCGCCGCGGGACTGAGGCGGGGGCAGAGCCGAAGAGACCGACACAGAGA A G TSC22D2 Ensembl:ENSG00000196428 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:150408733..150409233 26863196 MeRIP-seq:(Medium) rs536199923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934523,Human_RBP_ID_5241756,Human_RBP_ID_27823574 83228 RMVar_ID_83228 Human_SNP_ID_158130240 m1A Human chr3 + 150409142 150409142 150409142 GCCGCCGCGGGACTGAGACGGGGGCAGAGCCGAAGAGACCGACACAGAGAAGGAAACGAGGAGGA GCCGCCGCGGGACTGAGACGGGGGCAGAGCCGGAGAGACCGACACAGAGAAGGAAACGAGGAGGA A G TSC22D2 Ensembl:ENSG00000196428 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:150409021..150409222 26863196 MeRIP-seq:(Medium) rs1007525551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934523,Human_RBP_ID_5241756,Human_RBP_ID_27823574 83229 RMVar_ID_83229 Human_SNP_ID_158130471 m1A Human chr3 + 150409746 150409746 150409746 GCGGCGGCTGCCACTTCGGCCCCCGCCCCCGGAGCACCCGGCGGCCCCCAGCTCGCGGGCTCATC GCGGCGGCTGCCACTTCGGCCCCCGCCCCCGGGGCACCCGGCGGCCCCCAGCTCGCGGGCTCATC A G TSC22D2 Ensembl:ENSG00000196428 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:150409631..150409882 32194978 MeRIP-seq:(Medium) rs1470151604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_159337,Human_RBP_ID_784870,Human_RBP_ID_22091929 83230 RMVar_ID_83230 Human_SNP_ID_158130856 m1A Human chr3 + 150410523 150410523 150410523 CTGCAGCAGCACGTGGCCGGCCTGCAGCCGCCAAGCCCCGCGCAGCCCTCGTCCACCGGCGCCGC CTGCAGCAGCACGTGGCCGGCCTGCAGCCGCCGAGCCCCGCGCAGCCCTCGTCCACCGGCGCCGC A G TSC22D2 Ensembl:ENSG00000196428 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:150410426..150410640 26863410 MeRIP-seq:(Medium) rs1184500722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533877 83231 RMVar_ID_83231 Human_SNP_ID_158161206 m1A Human chr3 - 150544497 150544497 150544497 TTATTTTAATATTTGCTCTTTCTTTTTACAGCAATTTTCCAGATTATTCAAAGTATCAGGATGGG TTATTTTAATATTTGCTCTTTCTTTTTACAGCCATTTTCCAGATTATTCAAAGTATCAGGATGGG T G SERP1 Ensembl:ENSG00000120742 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr3:150544451..150544500;chr3:150544301..150544500 26863196,32194978 MeRIP-seq:(Medium) rs1330335810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2756205,Human_RBP_ID_17291603,Human_RBP_ID_17517721,Human_RBP_ID_22457522,Human_RBP_ID_23213623 Human_Splice_Rec_495914,Human_Splice_Rec_495920,Human_Splice_Rec_495922 83232 RMVar_ID_83232 Human_SNP_ID_158161805 m1A Human chr3 + 150546374 150546374 150546374 ACCGAGCGGGGCAGGTGCGCAGGAGGAAGAGAACTGGCCGCCGGGTCGTTCTCGCGCCGCCGTCG ACCGAGCGGGGCAGGTGCGCAGGAGGAAGAGAGCTGGCCGCCGGGTCGTTCTCGCGCCGCCGTCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:150546051..150546563 26863196 MeRIP-seq:(Medium) rs1412164652 Functional Loss SNV dbSNP153 33..33 33 - - - 83233 RMVar_ID_83233 Human_SNP_ID_158166098 m1A Human chr3 - 150564380 150564380 150564380 TAATAAAATTATGTCATAAATCTTTCCATACTAAAATTGTTGTTTTCAAAGAAGTGAACTTCATT TAATAAAATTATGTCATAAATCTTTCCATACTGAAATTGTTGTTTTCAAAGAAGTGAACTTCATT T C SERP1 Ensembl:ENSG00000120742 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:150564304..150564405 32194978 MeRIP-seq:(Medium) rs757486173 Functional Loss SNV dbSNP153 33..33 33 - - - 83234 RMVar_ID_83234 Human_SNP_ID_158166099 m1A Human chr3 - 150564380 150564380 150564380 TAATAAAATTATGTCATAAATCTTTCCATACTAAAATTGTTGTTTTCAAAGAAGTGAACTTCATT TAATAAAATTATGTCATAAATCTTTCCATACTCAAATTGTTGTTTTCAAAGAAGTGAACTTCATT T G SERP1 Ensembl:ENSG00000120742 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:150564304..150564405 32194978 MeRIP-seq:(Medium) rs757486173 Functional Loss SNV dbSNP153 33..33 33 - - - 83235 RMVar_ID_83235 Human_SNP_ID_158175240 m1A Human chr3 - 150603388 150603388 150603388 AGGCCTCGCTCCGGACCATCGCAGACGCCGCCACTAGGAGAAGCAGCAGAAGCCTCATCTTAAAT AGGCCTCGCTCCGGACCATCGCAGACGCCGCCGCTAGGAGAAGCAGCAGAAGCCTCATCTTAAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:150603341..150603432 26863196 MeRIP-seq:(Medium) rs1215142352 Functional Loss SNV dbSNP153 33..33 33 - - - 83236 RMVar_ID_83236 Human_SNP_ID_158175247 m1A Human chr3 - 150603396 150603396 150603396 ATTGGCCGAGGCCTCGCTCCGGACCATCGCAGACGCCGCCACTAGGAGAAGCAGCAGAAGCCTCA ATTGGCCGAGGCCTCGCTCCGGACCATCGCAGCCGCCGCCACTAGGAGAAGCAGCAGAAGCCTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:150603346..150603467 26863196 MeRIP-seq:(Medium) rs986819954 Functional Loss SNV dbSNP153 33..33 33 - - - 83237 RMVar_ID_83237 Human_SNP_ID_158175251 m1A Human chr3 + 150603402 150603402 150603402 TTCTGCTGCTTCTCCTAGTGGCGGCGTCTGCGATGGTCCGGAGCGAGGCCTCGGCCAATCTGGGC TTCTGCTGCTTCTCCTAGTGGCGGCGTCTGCGGTGGTCCGGAGCGAGGCCTCGGCCAATCTGGGC A G SELENOT Ensembl:ENSG00000198843 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr3:150603355..150603449;chr3:150603351..150603500 26863196,32194978 MeRIP-seq:(Medium) rs770297797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609754,Human_RBP_ID_4727236,Human_RBP_ID_9333911,Human_RBP_ID_25704735 Human_Splice_Rec_496181,Human_Splice_Rec_496193,Human_Splice_Rec_496203 83238 RMVar_ID_83238 Human_SNP_ID_158212936 m1A Human chr3 - 150762797 150762797 150762797 CGGCCCCAGCGCTAATAAACCCTGCAGCAAGCAGCCGCCGCCGCAGCCCCAGCACACTCCGTCCC CGGCCCCAGCGCTAATAAACCCTGCAGCAAGCGGCCGCCGCCGCAGCCCCAGCACACTCCGTCCC T C SIAH2 Ensembl:ENSG00000181788 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:150762620..150762945 26863196 MeRIP-seq:(Medium) rs1559939586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334317,Human_RBP_ID_18194951 RMVar_hsa_circ_92856,RMVar_hsa_circ_222184 83239 RMVar_ID_83239 Human_SNP_ID_158213030 m1A Human chr3 + 150763128 150763128 150763128 CGTCCCGGGCCCCGAACCCCAGCGGTGCGCAGAGCCCTGGCCCACCCGCTTCTGGAACAGCCGCT CGTCCCGGGCCCCGAACCCCAGCGGTGCGCAGGGCCCTGGCCCACCCGCTTCTGGAACAGCCGCT A G SIAH2-AS1 Ensembl:ENSG00000244265 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:150762982..150763140;chr3:150762596..150763135;chr3:150762585..150763150;chr3:150762626..150763150 26863196 MeRIP-seq:(Medium) rs1433790285 Functional Loss SNV dbSNP153 33..33 33 - - - 83240 RMVar_ID_83240 Human_SNP_ID_158213289 m1A Human chr3 + 150763921 150763921 150763921 GCAGCGTTGGCTAAGAGTTCGAGATCATCTAGAAATGTCAGAAACGTAGGTTGGGTCGTGAGGTC GCAGCGTTGGCTAAGAGTTCGAGATCATCTAGCAATGTCAGAAACGTAGGTTGGGTCGTGAGGTC A C SIAH2-AS1 Ensembl:ENSG00000244265 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:150763870..150763937 26863196 MeRIP-seq:(Medium) rs1252220669 Functional Loss SNV dbSNP153 33..33 33 - - - 83241 RMVar_ID_83241 Human_SNP_ID_158577927 m1A Human chr3 + 152266843 152266841 152266843 AGTCTGTCCACACCCATTCACCCCTCCATCCCACACTCTCATTCACCCTCCAAGCTGCCGTCACA AGTCTGTCCACACCCATTCACCCCTCCATCC__CACTCTCATTCACCCTCCAAGCTGCCGTCACA CCA C MBNL1 Ensembl:ENSG00000152601 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:152266799..152267085 26863196 MeRIP-seq:(Medium) rs755985518 Functional Loss DEL dbSNP153 32..33 33 - - - 83242 RMVar_ID_83242 Human_SNP_ID_158578584 m1A Human chr3 - 152269074 152269068 152269074 AAATGGAAACTTACCTCTCACATTTTTTTTTCAGAGGCGGCCCCACTGTCGACCAAGTGCCCAAG AAATGGAAACTTACCTCTCACATTTTTTTTTC______GGCCCCACTGTCGACCAAGTGCCCAAG CGCCTCT C MBNL1-AS1 Ensembl:ENSG00000229619 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:152269049..152269555 26863196 MeRIP-seq:(Medium) rs1559953103 Functional Loss DEL dbSNP153 33..38 33 - - - 83243 RMVar_ID_83243 Human_SNP_ID_158578587 m1A Human chr3 - 152269074 152269074 152269074 AAATGGAAACTTACCTCTCACATTTTTTTTTCAGAGGCGGCCCCACTGTCGACCAAGTGCCCAAG AAATGGAAACTTACCTCTCACATTTTTTTTTCGGAGGCGGCCCCACTGTCGACCAAGTGCCCAAG T C MBNL1-AS1 Ensembl:ENSG00000229619 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:152269049..152269555 26863196 MeRIP-seq:(Medium) rs780533628 Functional Loss SNV dbSNP153 33..33 33 - - - 83244 RMVar_ID_83244 Human_SNP_ID_158578764 m1A Human chr3 - 152269507 152269507 152269507 AACCGGGCGGGATGGCAGCCCCGGGGCCAGGGATGCGGGAGCCGCCGGGAAGACCCGCGCGCCGC AACCGGGCGGGATGGCAGCCCCGGGGCCAGGGTTGCGGGAGCCGCCGGGAAGACCCGCGCGCCGC T A MBNL1-AS1 Ensembl:ENSG00000229619 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:152269447..152269533 26863196 MeRIP-seq:(Medium) rs752618547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_497113,Human_Splice_Rec_497115,Human_Splice_Rec_497117 83245 RMVar_ID_83245 Human_SNP_ID_158792599 m1A Human chr3 + 153162328 153162328 153162328 GCGCGTCCCGGCCCGACGCGCAATTAGCAGCCACCTCCGCAGCCCGCCGCCACCGCCTCCCTGCC GCGCGTCCCGGCCCGACGCGCAATTAGCAGCCCCCTCCGCAGCCCGCCGCCACCGCCTCCCTGCC A C RAP2B Ensembl:ENSG00000181467 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:153162277..153162435 26863196 MeRIP-seq:(Medium) rs1025578704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_310432,Human_RBP_ID_4757518 83246 RMVar_ID_83246 Human_SNP_ID_159082097 m1A Human chr3 - 154324243 154324243 154324243 GGCGGCAGGGGCCGGCATCCCGGGCACCTGAAAGGCCGCGAAATCGGCATGTGGTACGCGAAAAA GGCGGCAGGGGCCGGCATCCCGGGCACCTGAAGGGCCGCGAAATCGGCATGTGGTACGCGAAAAA T C DHX36 Ensembl:ENSG00000174953 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:154324190..154324379 26863196 MeRIP-seq:(Medium) rs1287135753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965620,Human_RBP_ID_9334319,Human_RBP_ID_26347305 Human_Splice_Rec_497351,Human_Splice_Rec_497399,Human_Splice_Rec_497449,Human_Splice_Rec_497577 83247 RMVar_ID_83247 Human_SNP_ID_159082201 m1A Human chr3 + 154324428 154324428 154324428 CTGATGGTAGTCATAACTCATTGTCCTGGCAGACTACAACCCGTCAGAACCAGCAACCGCTGGAA CTGATGGTAGTCATAACTCATTGTCCTGGCAGGCTACAACCCGTCAGAACCAGCAACCGCTGGAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:154324313..154324448 26863196 MeRIP-seq:(Medium) rs777617377 Functional Loss SNV dbSNP153 33..33 33 - - - 83248 RMVar_ID_83248 Human_SNP_ID_159282877 m1A Human chr3 - 155142070 155142070 155142070 GCTTAAGTTTGGTTAAATATTCTGGAGCATAAACAACCACATCTTCCTCATTTGTAATACTAATA GCTTAAGTTTGGTTAAATATTCTGGAGCATAATCAACCACATCTTCCTCATTTGTAATACTAATA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:155142019..155142328 32194978 MeRIP-seq:(Medium) rs145615985 Functional Loss SNV dbSNP153 33..33 33 - - - 83249 RMVar_ID_83249 Human_SNP_ID_159465459 m1A Human chr3 - 155907833 155907833 155907833 GTACTGCTGTTTCCTCTTTCCCCAAATATCCAAAAAGGTTAGCACTTATTTTCTTCATGTCCAAT GTACTGCTGTTTCCTCTTTCCCCAAATATCCAGAAAGGTTAGCACTTATTTTCTTCATGTCCAAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:155907829..155908051 26863196 MeRIP-seq:(Medium) rs949193724 Functional Loss SNV dbSNP153 33..33 33 - - - 83250 RMVar_ID_83250 Human_SNP_ID_159484294 m1A Human chr3 + 155987852 155987852 155987852 TGGAAATCTGGAAAGGATTTGACGAAACGTTCAAGTCAAACACAGAATAAAGCCAGCAGGAAGAG TGGAAATCTGGAAAGGATTTGACGAAACGTTCGAGTCAAACACAGAATAAAGCCAGCAGGAAGAG A G SETP14 Ensembl:ENSG00000240489 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs185557603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3723402,Human_RBP_ID_17405847,Human_RBP_ID_18014503 83251 RMVar_ID_83251 Human_SNP_ID_159484363 m1A Human chr3 + 155988151 155988151 155988151 AGATGAAGATAATGATGAAGGGGAGGAAGGAGAGGAGGATGAAGGAGAAGATGACTAAATAGAAC AGATGAAGATAATGATGAAGGGGAGGAAGGAGGGGAGGATGAAGGAGAAGATGACTAAATAGAAC A G SETP14 Ensembl:ENSG00000240489 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:155987989..155988242;chr3:155988058..155988150 26863196 MeRIP-seq:(Medium) rs1383582309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1953415,Human_RBP_ID_2806772,Human_RBP_ID_4762255,Human_RBP_ID_7143107,Human_RBP_ID_10073886,Human_RBP_ID_14688114,Human_RBP_ID_23019182,Human_RBP_ID_23979369,Human_RBP_ID_26511837,Human_RBP_ID_27048065 Human_miRNA_ID_1839089 83252 RMVar_ID_83252 Human_SNP_ID_159484482 m1A Human chr3 + 155988495 155988495 155988495 AAAAAAGAAAAACCTGCTCCCTTCGCTCTGCTAGAAGCTGGAGGGTGCTAGGCCCCTGTGTAGTA AAAAAAGAAAAACCTGCTCCCTTCGCTCTGCTGGAAGCTGGAGGGTGCTAGGCCCCTGTGTAGTA A G lnc-GMPS-2 RNACentral:URS00008B367D lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1166371577 Functional Loss SNV dbSNP153 33..33 33 - - - 83253 RMVar_ID_83253 Human_SNP_ID_159611512 m1A Human chr3 - 156541440 156541440 156541440 TACTACTGCCTGGGTGGCAAGGGTGAGACTCCATCTCAAAAAAGAAACAAAAAAACCCAAAAAGT TACTACTGCCTGGGTGGCAAGGGTGAGACTCCGTCTCAAAAAAGAAACAAAAAAACCCAAAAAGT T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1224919387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247227,Human_RBP_ID_593574,Human_RBP_ID_7143715,Human_RBP_ID_18334292,Human_RBP_ID_22397635,Human_RBP_ID_26510618 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 83254 RMVar_ID_83254 Human_SNP_ID_159611546 m1A Human chr3 - 156541551 156541551 156541551 AAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGAA AAATTAGCCAGGCGTGATGGTGGGCGCCTGTAGTCTCAGCTACTTGGGAGGCTGAAGCAGGAGAA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1129099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 83255 RMVar_ID_83255 Human_SNP_ID_159611547 m1A Human chr3 - 156541552 156541552 156541552 AAAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGA AAAATTAGCCAGGCGTGATGGTGGGCGCCTGTGATCTCAGCTACTTGGGAGGCTGAAGCAGGAGA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1129097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26511387 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 83256 RMVar_ID_83256 Human_SNP_ID_159611557 m1A Human chr3 - 156541574 156541574 156541574 CCCCGTCTCTACTAAAAATACCAAAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTA CCCCGTCTCTACTAAAAATACCAAAATTAGCCGGGCGTGATGGTGGGCGCCTGTAATCTCAGCTA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1129091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 83257 RMVar_ID_83257 Human_SNP_ID_159612238 m1A Human chr3 + 156544366 156544366 156544366 GAAGAAGGAAGCAACAATGACCACGACCAGGAACAGAGTGTTGTTATAGAAGATGGAAAATGTTG GAAGAAGGAAGCAACAATGACCACGACCAGGAGCAGAGTGTTGTTATAGAAGATGGAAAATGTTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:156544301..156544400 32194978 MeRIP-seq:(Medium) rs373275961 Functional Loss SNV dbSNP153 33..33 33 - - - 83258 RMVar_ID_83258 Human_SNP_ID_159614823 m1A Human chr3 + 156555059 156555059 156555059 GCTGAAATCCTGCAGGAGCAGGTCCTCCTCAGACTGCTGTTTGGAGCTGCCTTTAGGAGCCATGG GCTGAAATCCTGCAGGAGCAGGTCCTCCTCAGCCTGCTGTTTGGAGCTGCCTTTAGGAGCCATGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:156555010..156555100 26863196 MeRIP-seq:(Medium) rs779502686 Functional Loss SNV dbSNP153 33..33 33 - - - 83259 RMVar_ID_83259 Human_SNP_ID_159642454 m1A Human chr3 + 156674757 156674757 156674757 GGCGCTGATCTCCGGCGCGGGCACTGCTTTCCACTCGGCTCCTGTCGTCCGTTCTCTCAGGCTCC GGCGCTGATCTCCGGCGCGGGCACTGCTTTCCCCTCGGCTCCTGTCGTCCGTTCTCTCAGGCTCC A C TIPARP Ensembl:ENSG00000163659 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:156674637..156674765 26863196 MeRIP-seq:(Medium) rs1429397019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70143,Human_RBP_ID_4728814,Human_RBP_ID_9302536,Human_RBP_ID_17997702,Human_RBP_ID_27499507 Human_Splice_Rec_498757 83260 RMVar_ID_83260 Human_SNP_ID_159676810 m1A Human chr3 + 156826123 156826123 156826123 CATCTCAGCAGTCGCTACCAAGCACCCGACCCACTCTCGCCCACCTCATCCCTCGATCCCCTTCC CATCTCAGCAGTCGCTACCAAGCACCCGACCCGCTCTCGCCCACCTCATCCCTCGATCCCCTTCC A G LEKR1 Ensembl:ENSG00000197980 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:156826081..156826152 26863196 MeRIP-seq:(Medium) rs1364995506 Functional Loss SNV dbSNP153 33..33 33 - - - 83261 RMVar_ID_83261 Human_SNP_ID_159751708 m1A Human chr3 - 157148225 157148225 157148225 GCAGGCACAGGCGCTGACTTTCTCTTCCTTTGAGCCTGCATCAGTTCTTGGTTTTGCCTATCTAC GCAGGCACAGGCGCTGACTTTCTCTTCCTTTGGGCCTGCATCAGTTCTTGGTTTTGCCTATCTAC T C CCNL1 Ensembl:ENSG00000163660 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:157148176..157148225 32194978 MeRIP-seq:(Medium) rs769435206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68344,Human_RBP_ID_1384506,Human_RBP_ID_1953553,Human_RBP_ID_7144182,Human_RBP_ID_8121470,Human_RBP_ID_8563148,Human_RBP_ID_14691055,Human_RBP_ID_18169505,Human_RBP_ID_18446180,Human_RBP_ID_22093159,Human_RBP_ID_26348814,Human_RBP_ID_27315086,Human_RBP_ID_27499554 RMVar_hsa_circ_222348,RMVar_hsa_circ_110601,RMVar_hsa_circ_101180,RMVar_hsa_circ_222347 83262 RMVar_ID_83262 Human_SNP_ID_159751750 m1A Human chr3 - 157148332 157148332 157148332 GAAACACAGGCATGAAAGGGGACATCATAGGGACAGGCGTGAACGATCTCGCTCCTTTGAGAGGT GAAACACAGGCATGAAAGGGGACATCATAGGGGCAGGCGTGAACGATCTCGCTCCTTTGAGAGGT T C CCNL1 Ensembl:ENSG00000163660 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:157148283..157148405 26863196 MeRIP-seq:(Medium) rs779270092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7144184,Human_RBP_ID_8563150,Human_RBP_ID_14691061,Human_RBP_ID_18800518,Human_RBP_ID_24561400 Human_miRNA_ID_2224961 RMVar_hsa_circ_222348,RMVar_hsa_circ_110601,RMVar_hsa_circ_101180,RMVar_hsa_circ_222347 83263 RMVar_ID_83263 Human_SNP_ID_159754789 m1A Human chr3 - 157160001 157159993 157160002 GCGCGGGCGGCTCCAGCTCCGGGACGACGACCACGACGACGACCACGACGGGAGGGATCCTGATC GCGCGGGCGGCTCCAGCTCCGGGACGACGAC_________GACCACGACGGGAGGGATCCTGATC CGTCGTCGTG C CCNL1 Ensembl:ENSG00000163660 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:157159951..157160150 26863196 MeRIP-seq:(Medium) rs759982653 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_247552,Human_RBP_ID_835901,Human_RBP_ID_4762331,Human_RBP_ID_9395604,Human_RBP_ID_22277778,Human_RBP_ID_23115957 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83264 RMVar_ID_83264 Human_SNP_ID_159754798 m1A Human chr3 - 157160001 157160001 157160001 GCGCGGGCGGCTCCAGCTCCGGGACGACGACCACGACGACGACCACGACGGGAGGGATCCTGATC GCGCGGGCGGCTCCAGCTCCGGGACGACGACCTCGACGACGACCACGACGGGAGGGATCCTGATC T A CCNL1 Ensembl:ENSG00000163660 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:157159951..157160150 26863196 MeRIP-seq:(Medium) rs527428547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247552,Human_RBP_ID_835901,Human_RBP_ID_4762331,Human_RBP_ID_9395604,Human_RBP_ID_22277778,Human_RBP_ID_23115957 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83265 RMVar_ID_83265 Human_SNP_ID_159754799 m1A Human chr3 - 157160001 157160001 157160001 GCGCGGGCGGCTCCAGCTCCGGGACGACGACCACGACGACGACCACGACGGGAGGGATCCTGATC GCGCGGGCGGCTCCAGCTCCGGGACGACGACCGCGACGACGACCACGACGGGAGGGATCCTGATC T C CCNL1 Ensembl:ENSG00000163660 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:157159951..157160150 26863196 MeRIP-seq:(Medium) rs527428547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247552,Human_RBP_ID_835901,Human_RBP_ID_4762331,Human_RBP_ID_9395604,Human_RBP_ID_22277778,Human_RBP_ID_23115957 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83266 RMVar_ID_83266 Human_SNP_ID_159754836 m1A Human chr3 - 157160073 157160071 157160074 TCGCTAAGACTATGGCGTCCGGGCCTCATTCGACAGCTACTGCTGCCGCAGCCGCCTCATCGGCC TCGCTAAGACTATGGCGTCCGGGCCTCATTC___AGCTACTGCTGCCGCAGCCGCCTCATCGGCC TGTC T CCNL1 Ensembl:ENSG00000163660 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:157160022..157160150 26863196 MeRIP-seq:(Medium) rs1273730831 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1621172,Human_RBP_ID_4757528,Human_RBP_ID_5505769,Human_RBP_ID_8563193,Human_RBP_ID_9333925,Human_RBP_ID_18424074,Human_RBP_ID_18800586,Human_RBP_ID_27823613 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83267 RMVar_ID_83267 Human_SNP_ID_159754837 m1A Human chr3 - 157160073 157160073 157160073 TCGCTAAGACTATGGCGTCCGGGCCTCATTCGACAGCTACTGCTGCCGCAGCCGCCTCATCGGCC TCGCTAAGACTATGGCGTCCGGGCCTCATTCGGCAGCTACTGCTGCCGCAGCCGCCTCATCGGCC T C CCNL1 Ensembl:ENSG00000163660 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:157160022..157160150 26863196 MeRIP-seq:(Medium) rs1222975862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1621172,Human_RBP_ID_4757528,Human_RBP_ID_5505769,Human_RBP_ID_8563193,Human_RBP_ID_9333925,Human_RBP_ID_18424074,Human_RBP_ID_18800586,Human_RBP_ID_27823613 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83268 RMVar_ID_83268 Human_SNP_ID_159754851 m1A Human chr3 - 157160099 157160099 157160099 CCGGCTGCGTTGGGCTTGCGTGCGGCTCGCTAAGACTATGGCGTCCGGGCCTCATTCGACAGCTA CCGGCTGCGTTGGGCTTGCGTGCGGCTCGCTATGACTATGGCGTCCGGGCCTCATTCGACAGCTA T A CCNL1 Ensembl:ENSG00000163660 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:157160004..157160150 26863196 MeRIP-seq:(Medium) rs1389933809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68362,Human_RBP_ID_783674,Human_RBP_ID_1384513,Human_RBP_ID_1621174,Human_RBP_ID_4728926,Human_RBP_ID_9333925,Human_RBP_ID_9394200,Human_RBP_ID_14691645,Human_RBP_ID_18424074,Human_RBP_ID_18800587,Human_RBP_ID_22088778,Human_RBP_ID_22277780,Human_RBP_ID_22822610,Human_RBP_ID_26347314,Human_RBP_ID_27822620 RMVar_hsa_circ_97774,RMVar_hsa_circ_113912,RMVar_hsa_circ_222349,RMVar_hsa_circ_222350 83269 RMVar_ID_83269 Human_SNP_ID_159754888 m1A Human chr3 + 157160149 157160149 157160149 GCCCAACGCAGCCGGAACCCGAAACAAGACTAACCAGCGTTCTCGGCGCGACGGATATTCCCGTG GCCCAACGCAGCCGGAACCCGAAACAAGACTACCCAGCGTTCTCGGCGCGACGGATATTCCCGTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:157160126..157160150 26863196 MeRIP-seq:(Medium) rs1255555830 Functional Loss SNV dbSNP153 33..33 33 - - - 83270 RMVar_ID_83270 Human_SNP_ID_159777292 m1A Human chr3 - 157251097 157251097 157251097 AGGAAAGAAAGAGAAAGAAAAGAAAGAAGGAAAGAAGAAAGGAAAGAAAGAAAGAAAGAAGAGAA AGGAAAGAAAGAGAAAGAAAAGAAAGAAGGAAGGAAGAAAGGAAAGAAAGAAAGAAAGAAGAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:157251046..157251132 26863196 MeRIP-seq:(Medium) rs961686619 Functional Loss SNV dbSNP153 33..33 33 - - - 83271 RMVar_ID_83271 Human_SNP_ID_159982330 m1A Human chr3 + 158102886 158102886 158102886 CATCCTCTTTGCGATCTTTCAGCTCCGGGGACACTGGAGGGGGCACCCCAGCGGGGCCACACGTG CATCCTCTTTGCGATCTTTCAGCTCCGGGGACCCTGGAGGGGGCACCCCAGCGGGGCCACACGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158102835..158102920 26863196 MeRIP-seq:(Medium) rs761764029 Functional Loss SNV dbSNP153 33..33 33 - - - 83272 RMVar_ID_83272 Human_SNP_ID_159982331 m1A Human chr3 + 158102886 158102886 158102886 CATCCTCTTTGCGATCTTTCAGCTCCGGGGACACTGGAGGGGGCACCCCAGCGGGGCCACACGTG CATCCTCTTTGCGATCTTTCAGCTCCGGGGACTCTGGAGGGGGCACCCCAGCGGGGCCACACGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158102835..158102920 26863196 MeRIP-seq:(Medium) rs761764029 Functional Loss SNV dbSNP153 33..33 33 - - - 83273 RMVar_ID_83273 Human_SNP_ID_159983009 m1A Human chr3 - 158105121 158105121 158105121 CAAAACTTCCCATTCTCTTTCAAGGTAGAAGGAAGCCAACGAAAGCTGAGGTCCAGGCTACGCTG CAAAACTTCCCATTCTCTTTCAAGGTAGAAGGGAGCCAACGAAAGCTGAGGTCCAGGCTACGCTG T C SHOX2 Ensembl:ENSG00000168779 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158105103..158105220 26863196 MeRIP-seq:(Medium) rs957898879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_499623,Human_Splice_Rec_499642,Human_Splice_Rec_499643,Human_Splice_Rec_499656,Human_Splice_Rec_499657 83274 RMVar_ID_83274 Human_SNP_ID_159983226 m1A Human chr3 - 158105758 158105755 158105758 GGAGGAGGAGGAGCAGGCGGAGGAGCTGGAGGAGGGCGCTCTCCCGTCCGGGAGCTGGACATGGG GGAGGAGGAGGAGCAGGCGGAGGAGCTGGAGG___GCGCTCTCCCGTCCGGGAGCTGGACATGGG CCCT C SHOX2 Ensembl:ENSG00000168779 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158105600..158106244 26863196 MeRIP-seq:(Medium) rs1398301062 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_27822623 Human_Splice_Rec_499631,Human_Splice_Rec_499641,Human_Splice_Rec_499649,Human_Splice_Rec_499655 83275 RMVar_ID_83275 Human_SNP_ID_159983241 m1A Human chr3 - 158105776 158105776 158105776 GGAGGCGGAGGAGGTGTAGGAGGAGGAGGAGCAGGCGGAGGAGCTGGAGGAGGGCGCTCTCCCGT GGAGGCGGAGGAGGTGTAGGAGGAGGAGGAGCCGGCGGAGGAGCTGGAGGAGGGCGCTCTCCCGT T G SHOX2 Ensembl:ENSG00000168779 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:158105699..158105792 26863410 MeRIP-seq:(Medium) rs573052538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_499631,Human_Splice_Rec_499641,Human_Splice_Rec_499649,Human_Splice_Rec_499655 83276 RMVar_ID_83276 Human_SNP_ID_159983375 m1A Human chr3 + 158105924 158105924 158105924 CGGTGCAGCCGGTCGGCTCCTTGGCCCCGCGCAGCGGCCCGCTCTCCAGCACCTCCCGGTACGTG CGGTGCAGCCGGTCGGCTCCTTGGCCCCGCGCCGCGGCCCGCTCTCCAGCACCTCCCGGTACGTG A C RSRC1 Ensembl:ENSG00000174891 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:158105618..158106110 26863196 MeRIP-seq:(Medium) rs1484829635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_499663 83277 RMVar_ID_83277 Human_SNP_ID_159984701 m1A Human chr3 - 158110416 158110416 158110416 CCCACCCACCCTACAGCCACCAGCCTTGACCCAAGGAGTCCGGAGCCTCCCAGGTGCGGGACGCA CCCACCCACCCTACAGCCACCAGCCTTGACCCGAGGAGTCCGGAGCCTCCCAGGTGCGGGACGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158110413..158110524 26863196 MeRIP-seq:(Medium) rs946616545 Functional Loss SNV dbSNP153 33..33 33 - - - 83278 RMVar_ID_83278 Human_SNP_ID_159987793 m1A Human chr3 + 158122150 158122150 158122150 CATCAGATACTGAAGAAGAAAGCAGAAGCAAGAGAAAAAAGAAACACCGTAGACGGTCCTCCTCG CATCAGATACTGAAGAAGAAAGCAGAAGCAAGGGAAAAAAGAAACACCGTAGACGGTCCTCCTCG A G RSRC1 Ensembl:ENSG00000174891 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:158122060..158122171 26863196 MeRIP-seq:(Medium) rs1463487590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26347315 Human_Splice_Rec_499664,Human_Splice_Rec_499682,Human_Splice_Rec_499688,Human_Splice_Rec_499706,Human_Splice_Rec_499718,Human_Splice_Rec_499734,Human_Splice_Rec_499752,Human_Splice_Rec_499768,Human_Splice_Rec_499784,Human_Splice_Rec_499804,Human_Splice_Rec_499810,Human_Splice_Rec_499820 RMVar_hsa_circ_94989,RMVar_hsa_circ_58867,RMVar_hsa_circ_283178,RMVar_hsa_circ_350917,RMVar_hsa_circ_222359,RMVar_hsa_circ_357129,RMVar_hsa_circ_331341,RMVar_hsa_circ_126924,RMVar_hsa_circ_274800,RMVar_hsa_circ_119544,RMVar_hsa_circ_222360,RMVar_hsa_circ_222362,RMVar_hsa_circ_222363,RMVar_hsa_circ_222361 83279 RMVar_ID_83279 Human_SNP_ID_159987795 m1A Human chr3 + 158122152 158122152 158122152 TCAGATACTGAAGAAGAAAGCAGAAGCAAGAGAAAAAAGAAACACCGTAGACGGTCCTCCTCGAG TCAGATACTGAAGAAGAAAGCAGAAGCAAGAGGAAAAAGAAACACCGTAGACGGTCCTCCTCGAG A G RSRC1 Ensembl:ENSG00000174891 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158122067..158122184 26863196 MeRIP-seq:(Medium) rs1396405813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26347315 Human_Splice_Rec_499664,Human_Splice_Rec_499682,Human_Splice_Rec_499688,Human_Splice_Rec_499706,Human_Splice_Rec_499718,Human_Splice_Rec_499734,Human_Splice_Rec_499752,Human_Splice_Rec_499768,Human_Splice_Rec_499784,Human_Splice_Rec_499804,Human_Splice_Rec_499810,Human_Splice_Rec_499820 RMVar_hsa_circ_94989,RMVar_hsa_circ_58867,RMVar_hsa_circ_283178,RMVar_hsa_circ_350917,RMVar_hsa_circ_222359,RMVar_hsa_circ_357129,RMVar_hsa_circ_331341,RMVar_hsa_circ_126924,RMVar_hsa_circ_274800,RMVar_hsa_circ_119544,RMVar_hsa_circ_222360,RMVar_hsa_circ_222362,RMVar_hsa_circ_222363,RMVar_hsa_circ_222361 83280 RMVar_ID_83280 Human_SNP_ID_160097377 m1A Human chr3 + 158571412 158571412 158571412 GCGGGAATTAAGGTATCGAGGGGAGCTATTTTAAGGGAAAAGAGCGAGTTTTAGAGGGCGAGAGA GCGGGAATTAAGGTATCGAGGGGAGCTATTTTTAGGGAAAAGAGCGAGTTTTAGAGGGCGAGAGA A T MLF1 Ensembl:ENSG00000178053 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158571404..158571642 26863196 MeRIP-seq:(Medium) rs746606604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3722706,Human_RBP_ID_8943585 83281 RMVar_ID_83281 Human_SNP_ID_160097384 m1A Human chr3 - 158571428 158571428 158571428 GAGTTACTCCGAATTCTCTCTCGCCCTCTAAAACTCGCTCTTTTCCCTTAAAATAGCTCCCCTCG GAGTTACTCCGAATTCTCTCTCGCCCTCTAAATCTCGCTCTTTTCCCTTAAAATAGCTCCCCTCG T A lnc-LXN-3 RNACentral:URS00008B36CA lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:158571422..158571549 26863196 MeRIP-seq:(Medium) rs773629370 Functional Loss SNV dbSNP153 33..33 33 - - - 83282 RMVar_ID_83282 Human_SNP_ID_160097916 m1A Human chr3 - 158572818 158572818 158572818 GGCCCTCAACTCTCTACCTCACGTCCTCAACCATCCTCCTGCGACCTCACGCCCCCAAACCCTCC GGCCCTCAACTCTCTACCTCACGTCCTCAACCCTCCTCCTGCGACCTCACGCCCCCAAACCCTCC T G lnc-LXN-3 RNACentral:URS00008B36CA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:158572735..158572939 26863196 MeRIP-seq:(Medium) rs17629390 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10076,GWAS_ID_10077,GWAS_ID_10078 83283 RMVar_ID_83283 Human_SNP_ID_160116048 m1A Human chr3 - 158644625 158644625 158644625 GCTGCAGCTCCCAGGAGTCTCATGGCAAGCGCAGAGCACGCGTCAAAGTCCCGTGGCGCCGGGTG GCTGCAGCTCCCAGGAGTCTCATGGCAAGCGCGGAGCACGCGTCAAAGTCCCGTGGCGCCGGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:158644576..158644725;chr3:158644576..158644687;chr3:158644576..158644700 26863196 MeRIP-seq:(Medium) rs1422714109 Functional Loss SNV dbSNP153 33..33 33 - - - 83284 RMVar_ID_83284 Human_SNP_ID_160116059 m1A Human chr3 - 158644645 158644645 158644645 CGCGCCCCAGAGCCGCGACGGCTGCAGCTCCCAGGAGTCTCATGGCAAGCGCAGAGCACGCGTCA CGCGCCCCAGAGCCGCGACGGCTGCAGCTCCCCGGAGTCTCATGGCAAGCGCAGAGCACGCGTCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:158644596..158644695 26863196 MeRIP-seq:(Medium) rs767710902 Functional Loss SNV dbSNP153 33..33 33 - - - 83285 RMVar_ID_83285 Human_SNP_ID_160121194 m1A Human chr3 + 158665418 158665418 158665418 ATCCCACATTTAAAGTATACTTTGACACTGAGAACAAAGAGACAGTTATATCTGGAATGGGAGAA ATCCCACATTTAAAGTATACTTTGACACTGAGGACAAAGAGACAGTTATATCTGGAATGGGAGAA A G GFM1 Ensembl:ENSG00000168827 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:158665368..158665468 32194978 MeRIP-seq:(Medium) rs562202513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1953957,Human_RBP_ID_14696684,Human_RBP_ID_19011011 Human_Splice_Rec_500172,Human_Splice_Rec_500173,Human_Splice_Rec_500202,Human_Splice_Rec_500203,Human_Splice_Rec_500228,Human_Splice_Rec_500229,Human_Splice_Rec_500260,Human_Splice_Rec_500261,Human_Splice_Rec_500290 Human_miRNA_ID_1213700,Human_miRNA_ID_1605440,Human_miRNA_ID_1679689,Human_miRNA_ID_2582714 RMVar_hsa_circ_58356,RMVar_hsa_circ_337332,RMVar_hsa_circ_222367,RMVar_hsa_circ_222372,RMVar_hsa_circ_82359,RMVar_hsa_circ_349715,RMVar_hsa_circ_43241,RMVar_hsa_circ_222374,RMVar_hsa_circ_19273,RMVar_hsa_circ_275876,RMVar_hsa_circ_310922,RMVar_hsa_circ_125391,RMVar_hsa_circ_222376,RMVar_hsa_circ_222377,RMVar_hsa_circ_222378,RMVar_hsa_circ_222375,RMVar_hsa_circ_80158,RMVar_hsa_circ_311784,RMVar_hsa_circ_363369,RMVar_hsa_circ_354771,RMVar_hsa_circ_222379,RMVar_hsa_circ_335800,RMVar_hsa_circ_222380,RMVar_hsa_circ_222381,RMVar_hsa_circ_222382,RMVar_hsa_circ_356761,RMVar_hsa_circ_360281,RMVar_hsa_circ_222384 83286 RMVar_ID_83286 Human_SNP_ID_160133524 m1A Human chr3 + 158717686 158717667 158717687 AAAAGATCCCTCTAGCTGGAGTGTGGAGAATGATGCTGGAGTGAGGAGTTGTGCAGAGTTAATGT AAAAGATCCCTCTA____________________GCTGGAGTGAGGAGTTGTGCAGAGTTAATGT AGCTGGAGTGTGGAGAATGAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158717678..158717802 26863196 MeRIP-seq:(Medium) rs572381426 Functional Loss DEL dbSNP153 15..34 33 - - - Human_RBP_ID_7146575,Human_RBP_ID_14697678 RMVar_hsa_circ_222378 83287 RMVar_ID_83287 Human_SNP_ID_160135067 m1A Human chr3 - 158724091 158724091 158724091 TGTGAACCCACCTGCCCTCTCCTCTCTAGCTCAGTACTCGACCATAGGCTGCTTTGTCAAAGCTC TGTGAACCCACCTGCCCTCTCCTCTCTAGCTCGGTACTCGACCATAGGCTGCTTTGTCAAAGCTC T C RARRES1 Ensembl:ENSG00000118849 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158724083..158724159 26863196 MeRIP-seq:(Medium) rs1344661876 Functional Loss SNV dbSNP153 33..33 33 - - - 83288 RMVar_ID_83288 Human_SNP_ID_160137105 m1A Human chr3 + 158732298 158732298 158732298 CTGAGGCTGCCCAGGGTCGTCGGGGTCCCCGGACCCCGCGGGCGCCGCCACCGGGGCGAGCAACA CTGAGGCTGCCCAGGGTCGTCGGGGTCCCCGGCCCCCGCGGGCGCCGCCACCGGGGCGAGCAACA A C MFSD1,AC080013.1 Ensembl:ENSG00000118855,Ensembl:ENSG00000240207 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:158732247..158733969;chr3:158732247..158732501 26863196 MeRIP-seq:(Medium) rs1194657718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8265425 RMVar_hsa_circ_222378 83289 RMVar_ID_83289 Human_SNP_ID_160152516 m1A Human chr3 - 158802140 158802138 158802141 TCCTCATCCTCCTCCTCCATTGCGCCCGCAGGAGACGGAGAGGGGAAAGTGGTGACAACTCCAAA TCCTCATCCTCCTCCTCCATTGCGCCCGCAG___ACGGAGAGGGGAAAGTGGTGACAACTCCAAA TCTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:158802089..158802255 26863196 MeRIP-seq:(Medium) rs1348287470 Functional Loss DEL dbSNP153 32..34 33 - - - 83290 RMVar_ID_83290 Human_SNP_ID_160152544 m1A Human chr3 - 158802200 158802200 158802200 GGGGCGGCCGGGGCACCTCTGTCGGCCTCGTCAGGGCCGCCTGCCAGGAGCGCCCGCGCTTCCTC GGGGCGGCCGGGGCACCTCTGTCGGCCTCGTCGGGGCCGCCTGCCAGGAGCGCCCGCGCTTCCTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:158802101..158802250 26863410 MeRIP-seq:(Medium) rs776172675 Functional Loss SNV dbSNP153 33..33 33 - - - 83291 RMVar_ID_83291 Human_SNP_ID_160160373 m1A Human chr3 - 158834710 158834710 158834710 CCAAGCACCATAAGCACCTGTCCCTCCTTTCCATCTTCACTACCACTGCCTTAATTCAAGGCCCA CCAAGCACCATAAGCACCTGTCCCTCCTTTCCGTCTTCACTACCACTGCCTTAATTCAAGGCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158834661..158834753 26863196 MeRIP-seq:(Medium) rs939851203 Functional Loss SNV dbSNP153 33..33 33 - - - 83292 RMVar_ID_83292 Human_SNP_ID_160383459 m1A Human chr3 - 159763189 159763189 159763189 CCACCTTCCTCCTCGCCGCTTCCTCTCCCTCCACCGCGCAGCTCCAGCCGCCTTGCCGCCGCCGC CCACCTTCCTCCTCGCCGCTTCCTCTCCCTCCCCCGCGCAGCTCCAGCCGCCTTGCCGCCGCCGC T G IQCJ-SCHIP1-AS1-001,IQCJ-SCHIP1-AS1-001:2,IQCJ-SCHIP1-AS1 RNACentral:URS0000D5CC19,RNACentral:URS0000D5A8D5,RNACentral:URS00008B9B0C lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:159763138..159763270 26863196 MeRIP-seq:(Medium) rs1268161586 Functional Loss SNV dbSNP153 33..33 33 - - - 83293 RMVar_ID_83293 Human_SNP_ID_160384008 m1A Human chr3 + 159764685 159764661 159764685 TGGGCGCCGGAGGAGGACGGGGAGGAGGAGGAAGAGGAGGACGAGCGCGACCAGCGAGGGTACCG TGGGCGCCG________________________GAGGAGGACGAGCGCGACCAGCGAGGGTACCG GGAGGAGGACGGGGAGGAGGAGGAA G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr3:159764316..159764854;chr3:159764642..159764790 26863196 MeRIP-seq:(Medium) rs1560040786 Functional Loss DEL dbSNP153 10..33 33 - - - RMVar_hsa_circ_222404,RMVar_hsa_circ_283101,RMVar_hsa_circ_287276,RMVar_hsa_circ_222403 83294 RMVar_ID_83294 Human_SNP_ID_160384218 m1A Human chr3 + 159765010 159765010 159765010 GGGGGCTCTGCCTTCAGCCCCCAGACGGCGGGACGTGCGTCCCCGAAGAGCCCCCGGTGCCACCT GGGGGCTCTGCCTTCAGCCCCCAGACGGCGGGGCGTGCGTCCCCGAAGAGCCCCCGGTGCCACCT A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:159764960..159765139 26863196 MeRIP-seq:(Medium) rs1237805366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_500805,Human_Splice_Rec_500821 RMVar_hsa_circ_222404,RMVar_hsa_circ_283101,RMVar_hsa_circ_287276,RMVar_hsa_circ_222403 83295 RMVar_ID_83295 Human_SNP_ID_160391240 m1A Human chr3 - 159796213 159796213 159796213 TTCTTAAAACTAGTATCTCCCCACTAGAATGCATTCTCACCACCATCAGACACCACTCCCCAACA TTCTTAAAACTAGTATCTCCCCACTAGAATGCCTTCTCACCACCATCAGACACCACTCCCCAACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:159796208..159796306 26863196 MeRIP-seq:(Medium) rs1008668533 Functional Loss SNV dbSNP153 33..33 33 - - - 83296 RMVar_ID_83296 Human_SNP_ID_160396822 m1A Human chr3 + 159822235 159822235 159822235 CAGGTGGGATTTAACCAAGTGAATATGAAGTGAGGGGGCAAGTGAGAATAATTGATTGAGTTAAG CAGGTGGGATTTAACCAAGTGAATATGAAGTGCGGGGGCAAGTGAGAATAATTGATTGAGTTAAG A C IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:159822233..159822538 26863196 MeRIP-seq:(Medium) rs1560068278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119097,RMVar_hsa_circ_222405 83297 RMVar_ID_83297 Human_SNP_ID_160396996 m1A Human chr3 + 159823072 159823072 159823072 GATGGACTTGGGGAGGAATAGGAGTTGGCCAGAGAGGGTTGGACAGAGCCATATGGAAAGGAGAG GATGGACTTGGGGAGGAATAGGAGTTGGCCAGGGAGGGTTGGACAGAGCCATATGGAAAGGAGAG A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:159823065..159823229 26863196 MeRIP-seq:(Medium) rs1453776772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119097,RMVar_hsa_circ_222405 83298 RMVar_ID_83298 Human_SNP_ID_160406664 m1A Human chr3 + 159866120 159866120 159866120 TTAGCAAGTTAGACTGCCTGTGGTTGTGCTATATCTGCCCACTTATCAGCATTTTTTATTTTCTT TTAGCAAGTTAGACTGCCTGTGGTTGTGCTATGTCTGCCCACTTATCAGCATTTTTTATTTTCTT A G IQCJ-SCHIP1,SCHIP1 Ensembl:ENSG00000283154,Ensembl:ENSG00000151967 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:159866116..159866183 26863196 MeRIP-seq:(Medium) rs758320425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3693734 RMVar_hsa_circ_119097,RMVar_hsa_circ_222405 83299 RMVar_ID_83299 Human_SNP_ID_160464639 m1A Human chr3 + 160101115 160101115 160101115 AGGGGAGAAAACGGAGAAGAGTTAAGGAGGATAAAAAGAAGCGAGATCGAGACCGGGTGGAGAAT AGGGGAGAAAACGGAGAAGAGTTAAGGAGGATTAAAAGAAGCGAGATCGAGACCGGGTGGAGAAT A T BRD7P2 Ensembl:ENSG00000184100 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:160101039..160101124 26863196 MeRIP-seq:(Medium) rs111583489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3723892,Human_RBP_ID_5101898,Human_RBP_ID_17406247,Human_RBP_ID_18517389,Human_RBP_ID_18536203 83300 RMVar_ID_83300 Human_SNP_ID_160494615 m1A Human chr3 + 160226139 160226121 160226139 CTGGACAGTGGCGGCGGCGGCCGGGGCCGGGGAGGCGGCGGGCGCTCGGACCCCTCCTGCGCCTC CTGGACAGTGGCGGC__________________GGCGGCGGGCGCTCGGACCCCTCCTGCGCCTC CGGCGGCCGGGGCCGGGGA C C3orf80 Ensembl:ENSG00000180044 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:160226022..160226199 26863196 MeRIP-seq:(Medium) rs1457646340 Functional Loss DEL dbSNP153 16..33 33 - - - 83301 RMVar_ID_83301 Human_SNP_ID_160494625 m1A Human chr3 + 160226139 160226139 160226139 CTGGACAGTGGCGGCGGCGGCCGGGGCCGGGGAGGCGGCGGGCGCTCGGACCCCTCCTGCGCCTC CTGGACAGTGGCGGCGGCGGCCGGGGCCGGGGGGGCGGCGGGCGCTCGGACCCCTCCTGCGCCTC A G C3orf80 Ensembl:ENSG00000180044 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:160226022..160226199 26863196 MeRIP-seq:(Medium) rs945541748 Functional Loss SNV dbSNP153 33..33 33 - - - 83302 RMVar_ID_83302 Human_SNP_ID_160534297 m1A Human chr3 + 160400846 160400846 160400846 GGCCCCAGCGACCATGCCCCGTAAAGGCACCCAGCCCTCCACTGCCCGGCGCAGAGAGGAAGGGC GGCCCCAGCGACCATGCCCCGTAAAGGCACCCGGCCCTCCACTGCCCGGCGCAGAGAGGAAGGGC A G SMC4 Ensembl:ENSG00000113810 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:160400801..160400938 26863196 MeRIP-seq:(Medium) rs747566736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_935994,Human_RBP_ID_4729476,Human_RBP_ID_9302537 Human_Splice_Rec_501440,Human_Splice_Rec_501454,Human_Splice_Rec_501484,Human_Splice_Rec_501500,Human_Splice_Rec_501546,Human_Splice_Rec_501592 Human_miRNA_ID_2456569,Human_miRNA_ID_2461480,Human_miRNA_ID_2634138,Human_miRNA_ID_2636825 RMVar_hsa_circ_222425,RMVar_hsa_circ_115162 83303 RMVar_ID_83303 Human_SNP_ID_160534313 m1A Human chr3 + 160400873 160400873 160400873 CACCCAGCCCTCCACTGCCCGGCGCAGAGAGGAAGGGCCGCCGCCGCCGTCCCCTGACGGCGCCA CACCCAGCCCTCCACTGCCCGGCGCAGAGAGGCAGGGCCGCCGCCGCCGTCCCCTGACGGCGCCA A C SMC4 Ensembl:ENSG00000113810 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:160400801..160400923;chr3:160400764..160400906 26863196 MeRIP-seq:(Medium) rs775088062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247121,Human_RBP_ID_9302538,Human_RBP_ID_23026395 Human_Splice_Rec_501440,Human_Splice_Rec_501441,Human_Splice_Rec_501449,Human_Splice_Rec_501454,Human_Splice_Rec_501455,Human_Splice_Rec_501484,Human_Splice_Rec_501485,Human_Splice_Rec_501500,Human_Splice_Rec_501501,Human_Splice_Rec_501546,Human_Splice_Rec_501547,Human_Splice_Rec_501592,Human_Splice_Rec_501593,Human_Splice_Rec_501619,Human_Splice_Rec_501633,Human_Splice_Rec_501677,Human_Splice_Rec_501689 RMVar_hsa_circ_222425,RMVar_hsa_circ_115162 83304 RMVar_ID_83304 Human_SNP_ID_160534323 m1A Human chr3 - 160400890 160400890 160400890 AGGCTCCGCGTCGCTGCTGGCGCCGTCAGGGGACGGCGGCGGCGGCCCTTCCTCTCTGCGCCGGG AGGCTCCGCGTCGCTGCTGGCGCCGTCAGGGGTCGGCGGCGGCGGCCCTTCCTCTCTGCGCCGGG T A AC079594.2 Ensembl:ENSG00000248710 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:160400801..160400950 32194978 MeRIP-seq:(Medium) rs764194681 Functional Loss SNV dbSNP153 33..33 33 - - - 83305 RMVar_ID_83305 Human_SNP_ID_160534726 m1A Human chr3 + 160401999 160401999 160401999 CATTCCTCCTCCCCCGCCTCCAGCAATGACCAATGAAGCTGGAGCTCCTCGGCTTATGATAACTC CATTCCTCCTCCCCCGCCTCCAGCAATGACCAGTGAAGCTGGAGCTCCTCGGCTTATGATAACTC A G SMC4 Ensembl:ENSG00000113810 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:160401901..160402025 32194978 MeRIP-seq:(Medium) rs1381764973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1954222,Human_RBP_ID_4729484,Human_RBP_ID_7148108,Human_RBP_ID_8869077,Human_RBP_ID_14702046,Human_RBP_ID_17998285 Human_Splice_Rec_501442,Human_Splice_Rec_501443,Human_Splice_Rec_501450,Human_Splice_Rec_501451,Human_Splice_Rec_501456,Human_Splice_Rec_501457,Human_Splice_Rec_501476,Human_Splice_Rec_501477,Human_Splice_Rec_501486,Human_Splice_Rec_501487,Human_Splice_Rec_501502,Human_Splice_Rec_501503,Human_Splice_Rec_501548,Human_Splice_Rec_501549,Human_Splice_Rec_501594,Human_Splice_Rec_501620,Human_Splice_Rec_501621,Human_Splice_Rec_501634,Human_Splice_Rec_501635,Human_Splice_Rec_501678,Human_Splice_Rec_501679,Human_Splice_Rec_501684,Human_Splice_Rec_501685,Human_Splice_Rec_501690,Human_Splice_Rec_501691 Human_miRNA_ID_724572,Human_miRNA_ID_2088643,Human_miRNA_ID_2291322,Human_miRNA_ID_2356667,Human_miRNA_ID_3059112 RMVar_hsa_circ_10556,RMVar_hsa_circ_31710,RMVar_hsa_circ_222425,RMVar_hsa_circ_115162,RMVar_hsa_circ_62770,RMVar_hsa_circ_18861 83306 RMVar_ID_83306 Human_SNP_ID_160575948 m1A Human chr3 - 160565439 160565439 160565439 GTTAGGGCGGGGGGGCGGGCGGGGAGAGGAGAAGGCCGCGGCGGAGGCAGGTGAGAGGAGGAAGG GTTAGGGCGGGGGGGCGGGCGGGGAGAGGAGAGGGCCGCGGCGGAGGCAGGTGAGAGGAGGAAGG T C KPNA4 Ensembl:ENSG00000186432 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:160565326..160565525 26863196 MeRIP-seq:(Medium) rs548785932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70397,Human_RBP_ID_1633043,Human_RBP_ID_3964325,Human_RBP_ID_4729801,Human_RBP_ID_5149805,Human_RBP_ID_5241620,Human_RBP_ID_5530710,Human_RBP_ID_8235847,Human_RBP_ID_8943517,Human_RBP_ID_9302544,Human_RBP_ID_9333932,Human_RBP_ID_9394214,Human_RBP_ID_9434713,Human_RBP_ID_17069314,Human_RBP_ID_17661001,Human_RBP_ID_18424078,Human_RBP_ID_18953899,Human_RBP_ID_24382122,Human_RBP_ID_26347343 83307 RMVar_ID_83307 Human_SNP_ID_160575949 m1A Human chr3 - 160565439 160565439 160565439 GTTAGGGCGGGGGGGCGGGCGGGGAGAGGAGAAGGCCGCGGCGGAGGCAGGTGAGAGGAGGAAGG GTTAGGGCGGGGGGGCGGGCGGGGAGAGGAGACGGCCGCGGCGGAGGCAGGTGAGAGGAGGAAGG T G KPNA4 Ensembl:ENSG00000186432 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:160565326..160565525 26863196 MeRIP-seq:(Medium) rs548785932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70397,Human_RBP_ID_1633043,Human_RBP_ID_3964325,Human_RBP_ID_4729801,Human_RBP_ID_5149805,Human_RBP_ID_5241620,Human_RBP_ID_5530710,Human_RBP_ID_8235847,Human_RBP_ID_8943517,Human_RBP_ID_9302544,Human_RBP_ID_9333932,Human_RBP_ID_9394214,Human_RBP_ID_9434713,Human_RBP_ID_17069314,Human_RBP_ID_17661001,Human_RBP_ID_18424078,Human_RBP_ID_18953899,Human_RBP_ID_24382122,Human_RBP_ID_26347343 83308 RMVar_ID_83308 Human_SNP_ID_160575986 m1A Human chr3 + 160565495 160565494 160565496 CGCCCTAACCCCAGCGCGACTGCAGCTCCGGCAAAGACAACTGTGGGGCCGGGCGGCGGCAAGGC CGCCCTAACCCCAGCGCGACTGCAGCTCCGGC__AGACAACTGTGGGGCCGGGCGGCGGCAAGGC CAA C KRT8P12 Ensembl:ENSG00000229320 Pseudogene exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:160565416..160565498 26863410 MeRIP-seq:(Medium) rs1202612949 Functional Loss DEL dbSNP153 33..34 33 - - - 83309 RMVar_ID_83309 Human_SNP_ID_160576152 m1A Human chr3 - 160565813 160565813 160565813 CTCCTTCCCCTTGCTGGTTTCCCCTTAAGTCTACTTCTCTATTGCTTCCAACCCCTCTCTCCGAA CTCCTTCCCCTTGCTGGTTTCCCCTTAAGTCTGCTTCTCTATTGCTTCCAACCCCTCTCTCCGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:160565763..160565858 26863196 MeRIP-seq:(Medium) rs1477430755 Functional Loss SNV dbSNP153 33..33 33 - - - 83310 RMVar_ID_83310 Human_SNP_ID_160576233 m1A Human chr3 + 160566147 160566147 160566147 ACGTGAGTTGAGGAGGCTCAGCGGAAAGCGACAGGAAAGGTGGGTGGAAAAGGAAAGGGCCCATT ACGTGAGTTGAGGAGGCTCAGCGGAAAGCGACGGGAAAGGTGGGTGGAAAAGGAAAGGGCCCATT A G KRT8P12 Ensembl:ENSG00000229320 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:160566096..160566216 26863196 MeRIP-seq:(Medium) rs150450512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17195271 Human_Splice_Rec_501887 83311 RMVar_ID_83311 Human_SNP_ID_160729131 m1A Human chr3 - 161221977 161221977 161221977 CTGTATGCCTTAAGTTCTTTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAGAATGTTGGGAT CTGTATGCCTTAAGTTCTTTTAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAGAGAATGTTGGGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:161221976..161222000 26863196 MeRIP-seq:(Medium) rs778154806 Functional Loss SNV dbSNP153 33..33 33 - - - 83312 RMVar_ID_83312 Human_SNP_ID_160824156 m1A Human chr3 + 161618427 161618427 161618427 TCAAGCTAAGTTTTGAATGACATGAAGGAGCCATATCTGAGGGCGGAGTTGCAGGCAGAGACCAG TCAAGCTAAGTTTTGAATGACATGAAGGAGCCGTATCTGAGGGCGGAGTTGCAGGCAGAGACCAG A G AC112770.1 Ensembl:ENSG00000288087 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:161618390..161618498 26863196 MeRIP-seq:(Medium) rs900781366 Functional Loss SNV dbSNP153 33..33 33 - - - 83313 RMVar_ID_83313 Human_SNP_ID_160838356 m1A Human chr3 + 161681960 161681960 161681960 AGAGAGTGATGGGGTGAGTGGTTTGGCGGGAAAAACGGTTGTGACAGAGCAGGTAATGGAATGAG AGAGAGTGATGGGGTGAGTGGTTTGGCGGGAAGAACGGTTGTGACAGAGCAGGTAATGGAATGAG A G AC112770.1 Ensembl:ENSG00000288087 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:161681956..161682085 26863196 MeRIP-seq:(Medium) rs1311524090 Functional Loss SNV dbSNP153 33..33 33 - - - 83314 RMVar_ID_83314 Human_SNP_ID_160850072 m1A Human chr3 + 161726580 161726580 161726580 GGTCGGGATGCGGAAATAAGGGATTGGGGCGCAGAGATATAAGAGGTCAGGGCGCAGAAATAAGG GGTCGGGATGCGGAAATAAGGGATTGGGGCGCGGAGATATAAGAGGTCAGGGCGCAGAAATAAGG A G AC112770.1 Ensembl:ENSG00000288087 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:161726490..161726620 26863196 MeRIP-seq:(Medium) rs1016245286 Functional Loss SNV dbSNP153 33..33 33 - - - 83315 RMVar_ID_83315 Human_SNP_ID_160875788 m1A Human chr3 + 161832614 161832614 161832614 ATTTGAGCAATAAACAAATTAAACCAAACAAAAATTTAGCTATAAGAGTTTTCTATCTAGTGGAT ATTTGAGCAATAAACAAATTAAACCAAACAAATATTTAGCTATAAGAGTTTTCTATCTAGTGGAT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:161832578..161832705 26863196 MeRIP-seq:(Medium) rs1013132773 Functional Loss SNV dbSNP153 33..33 33 - - - 83316 RMVar_ID_83316 Human_SNP_ID_160879451 m1A Human chr3 - 161846757 161846757 161846757 ACAACACGTCATGACTCCTCTTAGGCTTCCTGACACCTTCTTCATACTCATATCCCTTTCTCTAA ACAACACGTCATGACTCCTCTTAGGCTTCCTGGCACCTTCTTCATACTCATATCCCTTTCTCTAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:161846735..161846813 26863196 MeRIP-seq:(Medium) rs937746572 Functional Loss SNV dbSNP153 33..33 33 - - - 83317 RMVar_ID_83317 Human_SNP_ID_686079338 m1A Human chr20 + 60244530 60244530 60244530 AAAAGGAAGAGAGTGAGGAGAGAGGGAGATGGATGGATGGATGGGAAAGGAGAAGAAAAGGTAGA AAAAGGAAGAGAGTGAGGAGAGAGGGAGATGGTTGGATGGATGGGAAAGGAGAAGAAAAGGTAGA A T MIR646HG Ensembl:ENSG00000228340 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:60244479..60244662 26863196 MeRIP-seq:(Medium) rs1004359205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7017915 83318 RMVar_ID_83318 Human_SNP_ID_686434327 m1A Human chr20 - 61565290 61565284 61565290 GCACCGCCACCACCAAGAGCACCGCCACCACCATCACCCCATCACCAAGAGGACCACCACCACCA GCACCGCCACCACCAAGAGCACCGCCACCACC______CCATCACCAAGAGGACCACCACCACCA GGGTGAT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:61565249..61565362 26863196 MeRIP-seq:(Medium) rs1301474236 Functional Loss DEL dbSNP153 33..38 33 - - - 83319 RMVar_ID_83319 Human_SNP_ID_686434341 m1A Human chr20 - 61565290 61565288 61565290 GCACCGCCACCACCAAGAGCACCGCCACCACCATCACCCCATCACCAAGAGGACCACCACCACCA GCACCGCCACCACCAAGAGCACCGCCACCACC__CACCCCATCACCAAGAGGACCACCACCACCA GAT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:61565249..61565362 26863196 MeRIP-seq:(Medium) rs1568688842 Functional Loss DEL dbSNP153 33..34 33 - - - 83320 RMVar_ID_83320 Human_SNP_ID_686434345 m1A Human chr20 - 61565290 61565289 61565290 GCACCGCCACCACCAAGAGCACCGCCACCACCATCACCCCATCACCAAGAGGACCACCACCACCA GCACCGCCACCACCAAGAGCACCGCCACCACC_TCACCCCATCACCAAGAGGACCACCACCACCA AT A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:61565249..61565362 26863196 MeRIP-seq:(Medium) rs1568688855 Functional Loss DEL dbSNP153 33..33 33 - - - 83321 RMVar_ID_83321 Human_SNP_ID_686434350 m1A Human chr20 - 61565290 61565290 61565290 GCACCGCCACCACCAAGAGCACCGCCACCACCATCACCCCATCACCAAGAGGACCACCACCACCA GCACCGCCACCACCAAGAGCACCGCCACCACCTTCACCCCATCACCAAGAGGACCACCACCACCA T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:61565249..61565362 26863196 MeRIP-seq:(Medium) rs890888288 Functional Loss SNV dbSNP153 33..33 33 - - - 83322 RMVar_ID_83322 Human_SNP_ID_686557703 m1A Human chr20 + 61981712 61981712 61981712 CGAATCTCCCCCTCAGGCAGAGTGGGACATTCACACCATGACCCAGGAGACGTTCACAAAAGACA CGAATCTCCCCCTCAGGCAGAGTGGGACATTCGCACCATGACCCAGGAGACGTTCACAAAAGACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:61981710..61981807 26863196 MeRIP-seq:(Medium) rs917078773 Functional Loss SNV dbSNP153 33..33 33 - - - 83323 RMVar_ID_83323 Human_SNP_ID_686557776 m1A Human chr20 - 61981900 61981900 61981900 TGGTGTCTCCTATCGGGTGGGGTGTGGGTTTGATGTCTCCTCTCGGGTGGGGTGTGAGTTTGGTG TGGTGTCTCCTATCGGGTGGGGTGTGGGTTTGTTGTCTCCTCTCGGGTGGGGTGTGAGTTTGGTG T A TAF4 Ensembl:ENSG00000130699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:61981895..61981962 26863196 MeRIP-seq:(Medium) rs79811504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354040,Human_RBP_ID_9430867,Human_RBP_ID_18950804 RMVar_hsa_circ_211138,RMVar_hsa_circ_121037 83324 RMVar_ID_83324 Human_SNP_ID_686557777 m1A Human chr20 - 61981900 61981900 61981900 TGGTGTCTCCTATCGGGTGGGGTGTGGGTTTGATGTCTCCTCTCGGGTGGGGTGTGAGTTTGGTG TGGTGTCTCCTATCGGGTGGGGTGTGGGTTTGGTGTCTCCTCTCGGGTGGGGTGTGAGTTTGGTG T C TAF4 Ensembl:ENSG00000130699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:61981895..61981962 26863196 MeRIP-seq:(Medium) rs79811504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354040,Human_RBP_ID_9430867,Human_RBP_ID_18950804 RMVar_hsa_circ_211138,RMVar_hsa_circ_121037 83325 RMVar_ID_83325 Human_SNP_ID_686557854 m1A Human chr20 + 61982046 61982046 61982046 CCGAGAGGAGACATCAAACCCACACCCCACCCAAGAGGAGACACCAAACCCACACCCCACCCGAG CCGAGAGGAGACATCAAACCCACACCCCACCCCAGAGGAGACACCAAACCCACACCCCACCCGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:61982043..61982677 26863196 MeRIP-seq:(Medium) rs369741784 Functional Loss SNV dbSNP153 33..33 33 - - - 83326 RMVar_ID_83326 Human_SNP_ID_686557855 m1A Human chr20 + 61982046 61982046 61982046 CCGAGAGGAGACATCAAACCCACACCCCACCCAAGAGGAGACACCAAACCCACACCCCACCCGAG CCGAGAGGAGACATCAAACCCACACCCCACCCGAGAGGAGACACCAAACCCACACCCCACCCGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:61982043..61982677 26863196 MeRIP-seq:(Medium) rs369741784 Functional Loss SNV dbSNP153 33..33 33 - - - 83327 RMVar_ID_83327 Human_SNP_ID_686562664 m1A Human chr20 - 61997619 61997619 61997619 GCACAAATGAGACAGCGGGACGCCAACCTCACAGCACTAGCAGCGATCGGGCCCAGGAAAAAGAG GCACAAATGAGACAGCGGGACGCCAACCTCACGGCACTAGCAGCGATCGGGCCCAGGAAAAAGAG T C TAF4 Ensembl:ENSG00000130699 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:61997551..61997700 26863196 MeRIP-seq:(Medium) rs1290876444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926133,Human_RBP_ID_9389613,Human_RBP_ID_17192959,Human_RBP_ID_17975324,Human_RBP_ID_19106891 Human_Splice_Rec_2100628,Human_Splice_Rec_2100629,Human_Splice_Rec_2100654,Human_Splice_Rec_2100655,Human_Splice_Rec_2100672,Human_Splice_Rec_2100673 Human_miRNA_ID_2007912,Human_miRNA_ID_2673541,Human_miRNA_ID_2775924 RMVar_hsa_circ_211139,RMVar_hsa_circ_68368,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_321507,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_211140 83328 RMVar_ID_83328 Human_SNP_ID_686562665 m1A Human chr20 - 61997619 61997619 61997619 GCACAAATGAGACAGCGGGACGCCAACCTCACAGCACTAGCAGCGATCGGGCCCAGGAAAAAGAG GCACAAATGAGACAGCGGGACGCCAACCTCACCGCACTAGCAGCGATCGGGCCCAGGAAAAAGAG T G TAF4 Ensembl:ENSG00000130699 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:61997551..61997700 26863196 MeRIP-seq:(Medium) rs1290876444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926133,Human_RBP_ID_9389613,Human_RBP_ID_17192959,Human_RBP_ID_17975324,Human_RBP_ID_19106891 Human_Splice_Rec_2100628,Human_Splice_Rec_2100629,Human_Splice_Rec_2100654,Human_Splice_Rec_2100655,Human_Splice_Rec_2100672,Human_Splice_Rec_2100673 Human_miRNA_ID_2007912,Human_miRNA_ID_2673541,Human_miRNA_ID_2775924 RMVar_hsa_circ_211139,RMVar_hsa_circ_68368,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_321507,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_211140 83329 RMVar_ID_83329 Human_SNP_ID_686563065 m1A Human chr20 - 61998933 61998933 61998933 GCTGCTGCCGTCTGGGCACCTCCGTCTCAGCCACAACCTGATGAGCTCACTGAGACAGTGGGGTT GCTGCTGCCGTCTGGGCACCTCCGTCTCAGCCGCAACCTGATGAGCTCACTGAGACAGTGGGGTT T C TAF4 Ensembl:ENSG00000130699 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:61998931..61999060 26863196 MeRIP-seq:(Medium) rs780813293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211139,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_321507,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_211140,RMVar_hsa_circ_211142,RMVar_hsa_circ_365028 83330 RMVar_ID_83330 Human_SNP_ID_686564602 m1A Human chr20 - 62003784 62003784 62003784 GACACCCATGGTCGCCCTGCGGCAGCCTCACAACCGGATCATGCTCACCACGCCTCAGCAGATCC GACACCCATGGTCGCCCTGCGGCAGCCTCACAGCCGGATCATGCTCACCACGCCTCAGCAGATCC T C TAF4 Ensembl:ENSG00000130699 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62003699..62003812 26863196 MeRIP-seq:(Medium) rs1201997147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8856656,Human_RBP_ID_14159991,Human_RBP_ID_18776434,Human_RBP_ID_27487837 Human_Splice_Rec_2100644,Human_Splice_Rec_2100645,Human_Splice_Rec_2100662,Human_Splice_Rec_2100663,Human_Splice_Rec_2100682,Human_Splice_Rec_2100683 RMVar_hsa_circ_11043,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_211140,RMVar_hsa_circ_112213,RMVar_hsa_circ_211142,RMVar_hsa_circ_365028,RMVar_hsa_circ_302636,RMVar_hsa_circ_211143,RMVar_hsa_circ_211144 83331 RMVar_ID_83331 Human_SNP_ID_686565501 m1A Human chr20 + 62006595 62006595 62006595 GGCTGAGCACAGGGGGCTGGAGGGCACTGGTCACGGTGGCCGCCGTCTTCCCGGCCGTGCGCTGG GGCTGAGCACAGGGGGCTGGAGGGCACTGGTCTCGGTGGCCGCCGTCTTCCCGGCCGTGCGCTGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62006551..62006725 26863196 MeRIP-seq:(Medium) rs1452204816 Functional Loss SNV dbSNP153 33..33 33 - - - 83332 RMVar_ID_83332 Human_SNP_ID_686565789 m1A Human chr20 + 62007498 62007498 62007498 CTCGCCCTGCACACTTGGTGCATCTGCGCCCCACCCCTCCCTGGCCCTACTGCTCGCAGGCACCG CTCGCCCTGCACACTTGGTGCATCTGCGCCCCTCCCCTCCCTGGCCCTACTGCTCGCAGGCACCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62007494..62007576 26863196 MeRIP-seq:(Medium) rs1251598845 Functional Loss SNV dbSNP153 33..33 33 - - - 83333 RMVar_ID_83333 Human_SNP_ID_686565803 m1A Human chr20 - 62007519 62007519 62007519 TGAAGGTAATTTCAAAGGCCCCGGTGCCTGCGAGCAGTAGGGCCAGGGAGGGGTGGGGCGCAGAT TGAAGGTAATTTCAAAGGCCCCGGTGCCTGCGGGCAGTAGGGCCAGGGAGGGGTGGGGCGCAGAT T C TAF4 Ensembl:ENSG00000130699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62007516..62007584 26863196 MeRIP-seq:(Medium) rs754449757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19108981 RMVar_hsa_circ_11043,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_112213,RMVar_hsa_circ_211142,RMVar_hsa_circ_365028,RMVar_hsa_circ_211143,RMVar_hsa_circ_267916 83334 RMVar_ID_83334 Human_SNP_ID_686566267 m1A Human chr20 - 62008994 62008994 62008994 CTTTCCCCTAAAGCCTGTTGCATAGGACAGACACCTGTTGCTGCTGTGACCTGTGCCCGGGAGGC CTTTCCCCTAAAGCCTGTTGCATAGGACAGACGCCTGTTGCTGCTGTGACCTGTGCCCGGGAGGC T C TAF4 Ensembl:ENSG00000130699 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:62008991..62009076 26863410 MeRIP-seq:(Medium) rs1231142689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5383978,Human_RBP_ID_23258347 RMVar_hsa_circ_11043,RMVar_hsa_circ_211138,RMVar_hsa_circ_121037,RMVar_hsa_circ_367172,RMVar_hsa_circ_276742,RMVar_hsa_circ_211141,RMVar_hsa_circ_3601,RMVar_hsa_circ_112213,RMVar_hsa_circ_211142,RMVar_hsa_circ_365028,RMVar_hsa_circ_211143,RMVar_hsa_circ_211145,RMVar_hsa_circ_267916,RMVar_hsa_circ_327321 83335 RMVar_ID_83335 Human_SNP_ID_686570249 m1A Human chr20 + 62021366 62021366 62021366 GGATGAAGCAGAAGGGAGGAACAGGCATGGCCAGGCACAGGGTCCGGAGGGCCAGGGCGCTGGGG GGATGAAGCAGAAGGGAGGAACAGGCATGGCCCGGCACAGGGTCCGGAGGGCCAGGGCGCTGGGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62021362..62021522 32194978 MeRIP-seq:(Medium) rs1021146473 Functional Loss SNV dbSNP153 33..33 33 - - - 83336 RMVar_ID_83336 Human_SNP_ID_686579388 m1A Human chr20 + 62051543 62051543 62051543 TGCAGCATGAGTCCCATCCACCGTTCACTCCCACCCCTCTCACCGCCATAGGACACAGGGCTGGG TGCAGCATGAGTCCCATCCACCGTTCACTCCCGCCCCTCTCACCGCCATAGGACACAGGGCTGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62051539..62051752 26863196 MeRIP-seq:(Medium) rs1354969739 Functional Loss SNV dbSNP153 33..33 33 - - - 83337 RMVar_ID_83337 Human_SNP_ID_686579661 m1A Human chr20 + 62052387 62052387 62052387 AAACAAAGAAACTGTCCTTTGACCCCCTCACCACAGTCAGTGACCTACTTCTCCATCTCCTCCTG AAACAAAGAAACTGTCCTTTGACCCCCTCACCGCAGTCAGTGACCTACTTCTCCATCTCCTCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62052381..62052602 26863196 MeRIP-seq:(Medium) rs1214395462 Functional Loss SNV dbSNP153 33..33 33 - - - 83338 RMVar_ID_83338 Human_SNP_ID_686579815 m1A Human chr20 + 62052823 62052823 62052823 TCCCTCACACCACCCCACCCCCACAGTACCAGATCCCTCGCGCCATCCCCCATATCCCAGGTCCC TCCCTCACACCACCCCACCCCCACAGTACCAGGTCCCTCGCGCCATCCCCCATATCCCAGGTCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62052820..62052965 26863196 MeRIP-seq:(Medium) rs1189025190 Functional Loss SNV dbSNP153 33..33 33 - - - 83339 RMVar_ID_83339 Human_SNP_ID_686583658 m1A Human chr20 + 62064574 62064574 62064574 AATCCCGCTGGTGGTGGCCGTGGGCGTCCGGGACAGGCTCTGGGTCACTGCGCCGGCCGCGCCTT AATCCCGCTGGTGGTGGCCGTGGGCGTCCGGGGCAGGCTCTGGGTCACTGCGCCGGCCGCGCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62064523..62064792 26863196 MeRIP-seq:(Medium) rs1239287576 Functional Loss SNV dbSNP153 33..33 33 - - - 83340 RMVar_ID_83340 Human_SNP_ID_686584296 m1A Human chr20 - 62065460 62065460 62065460 CCCCCCTCACCGCGCCGCCCCCTTGTCCCCGCAGGGCCCGCGCCGCCCGCCGCGAAGCTGAGGCC CCCCCCTCACCGCGCCGCCCCCTTGTCCCCGCTGGGCCCGCGCCGCCCGCCGCGAAGCTGAGGCC T A TAF4 Ensembl:ENSG00000130699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62065424..62065508 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_926143,Human_RBP_ID_5385498,Human_RBP_ID_19106903,Human_RBP_ID_22549422,Human_RBP_ID_23258348,Human_RBP_ID_26788589 RMVar_hsa_circ_267916 83341 RMVar_ID_83341 Human_SNP_ID_686584297 m1A Human chr20 - 62065460 62065460 62065460 CCCCCCTCACCGCGCCGCCCCCTTGTCCCCGCAGGGCCCGCGCCGCCCGCCGCGAAGCTGAGGCC CCCCCCTCACCGCGCCGCCCCCTTGTCCCCGCGGGGCCCGCGCCGCCCGCCGCGAAGCTGAGGCC T C TAF4 Ensembl:ENSG00000130699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62065424..62065508 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_926143,Human_RBP_ID_5385498,Human_RBP_ID_19106903,Human_RBP_ID_22549422,Human_RBP_ID_23258348,Human_RBP_ID_26788589 RMVar_hsa_circ_267916 83342 RMVar_ID_83342 Human_SNP_ID_686584426 m1A Human chr20 + 62065777 62065777 62065777 CACCACTTTCTCGTCCACCTCGCTGTTGAAGAAGACCTCGTCCAGCAGATCCGAGCCCGCCGCCA CACCACTTTCTCGTCCACCTCGCTGTTGAAGACGACCTCGTCCAGCAGATCCGAGCCCGCCGCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62065584..62065835 26863196 MeRIP-seq:(Medium) rs745459805 Functional Loss SNV dbSNP153 33..33 33 - - - 83343 RMVar_ID_83343 Human_SNP_ID_686584653 m1A Human chr20 + 62066090 62066090 62066090 GCCGGGGCGCGGGCGGTCGGCCGGGGTGCGGCAGCAGCGGCGGGAAGCGCGGGGGCTGGAGCTCA GCCGGGGCGCGGGCGGTCGGCCGGGGTGCGGCCGCAGCGGCGGGAAGCGCGGGGGCTGGAGCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62066040..62066457 26863196 MeRIP-seq:(Medium) rs534068765 Functional Loss SNV dbSNP153 33..33 33 - - - 83344 RMVar_ID_83344 Human_SNP_ID_686584654 m1A Human chr20 + 62066090 62066090 62066090 GCCGGGGCGCGGGCGGTCGGCCGGGGTGCGGCAGCAGCGGCGGGAAGCGCGGGGGCTGGAGCTCA GCCGGGGCGCGGGCGGTCGGCCGGGGTGCGGCGGCAGCGGCGGGAAGCGCGGGGGCTGGAGCTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62066040..62066457 26863196 MeRIP-seq:(Medium) rs534068765 Functional Loss SNV dbSNP153 33..33 33 - - - 83345 RMVar_ID_83345 Human_SNP_ID_686584691 m1A Human chr20 + 62066156 62066156 62066156 GGGCGCGGGCGCCGGGGCGGTGGCGGACGGGGAGGGGGCCGCCGGGCGGGGCGCGGGATGCGGGA GGGCGCGGGCGCCGGGGCGGTGGCGGACGGGGGGGGGGCCGCCGGGCGGGGCGCGGGATGCGGGA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:62066058..62066210 26863196 MeRIP-seq:(Medium) rs1029534334 Functional Loss SNV dbSNP153 33..33 33 - - - 83346 RMVar_ID_83346 Human_SNP_ID_686584701 m1A Human chr20 + 62066188 62066188 62066188 AGGGGGCCGCCGGGCGGGGCGCGGGATGCGGGAACGGTGCGCTGGGCCGGGCCGAGGCGGGCGCG AGGGGGCCGCCGGGCGGGGCGCGGGATGCGGGGACGGTGCGCTGGGCCGGGCCGAGGCGGGCGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62066060..62066674 26863196 MeRIP-seq:(Medium) rs1227531967 Functional Loss SNV dbSNP153 33..33 33 - - - 83347 RMVar_ID_83347 Human_SNP_ID_686584865 m1A Human chr20 + 62066586 62066585 62066586 CGCACGGCTCTTCTCGCCCTCCAATCGTGACCACCCCTGGCCCTTCCCTCCATTTTTAATCAATA CGCACGGCTCTTCTCGCCCTCCAATCGTGACC_CCCCTGGCCCTTCCCTCCATTTTTAATCAATA CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62066542..62066701 26863196 MeRIP-seq:(Medium) rs1568948303 Functional Loss DEL dbSNP153 33..33 33 - - - 83348 RMVar_ID_83348 Human_SNP_ID_686584868 m1A Human chr20 + 62066586 62066586 62066586 CGCACGGCTCTTCTCGCCCTCCAATCGTGACCACCCCTGGCCCTTCCCTCCATTTTTAATCAATA CGCACGGCTCTTCTCGCCCTCCAATCGTGACCGCCCCTGGCCCTTCCCTCCATTTTTAATCAATA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62066542..62066701 26863196 MeRIP-seq:(Medium) rs933588781 Functional Loss SNV dbSNP153 33..33 33 - - - 83349 RMVar_ID_83349 Human_SNP_ID_686600486 m1A Human chr20 + 62122536 62122536 62122536 TGCCCGCGCAGGCCCCTCGGGCGGTGGCGAGGAGGCGCCCAGGCGGAGGCGGCGGCGGGCGGAGG TGCCCGCGCAGGCCCCTCGGGCGGTGGCGAGGGGGCGCCCAGGCGGAGGCGGCGGCGGGCGGAGG A G LSM14B Ensembl:ENSG00000149657 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62122451..62122700 26863196 MeRIP-seq:(Medium) rs1040885426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659505,Human_RBP_ID_18423191,Human_RBP_ID_26787974 RMVar_hsa_circ_120149,RMVar_hsa_circ_211148 83350 RMVar_ID_83350 Human_SNP_ID_686600498 m1A Human chr20 + 62122588 62122588 62122588 CGGCGGGCGGAGGAGCGCAGGAGCGGGCGGCCAGGCCACCGCGCGGCGGCGGAGCGGGCCGCGGC CGGCGGGCGGAGGAGCGCAGGAGCGGGCGGCCCGGCCACCGCGCGGCGGCGGAGCGGGCCGCGGC A C LSM14B Ensembl:ENSG00000149657 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:62122476..62122750 26863410 MeRIP-seq:(Medium) rs1164173223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659505,Human_RBP_ID_18423191 RMVar_hsa_circ_120149,RMVar_hsa_circ_211148 83351 RMVar_ID_83351 Human_SNP_ID_686600519 m1A Human chr20 + 62122652 62122652 62122652 CCCGGCGCTCCTTCCCCACCGCGGCCCGACGCACCCCGGCCGCCGCCATGAGCGGCTCCTCAGGC CCCGGCGCTCCTTCCCCACCGCGGCCCGACGCCCCCCGGCCGCCGCCATGAGCGGCTCCTCAGGC A C LSM14B Ensembl:ENSG00000149657 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr20:62122451..62122939;chr20:62122609..62122725 26863196,32194978 MeRIP-seq:(Medium) rs767775489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4655417,Human_RBP_ID_18423191 RMVar_hsa_circ_120149,RMVar_hsa_circ_211148 83352 RMVar_ID_83352 Human_SNP_ID_686601177 m1A Human chr20 + 62124749 62124749 62124749 TATCACTGTGTGTGAACCTCCGAAAGCTCAGCACACACTCCCGCAGGATCCCGCCATTGTTCAGG TATCACTGTGTGTGAACCTCCGAAAGCTCAGCTCACACTCCCGCAGGATCCCGCCATTGTTCAGG A T LSM14B Ensembl:ENSG00000149657 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62124568..62124812 26863196 MeRIP-seq:(Medium) rs1368700007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9391069,Human_RBP_ID_19106904 Human_Splice_Rec_2100701,Human_Splice_Rec_2100707,Human_Splice_Rec_2100723,Human_Splice_Rec_2100733,Human_Splice_Rec_2100741 Human_miRNA_ID_1961089,Human_miRNA_ID_2910838 RMVar_hsa_circ_120149,RMVar_hsa_circ_211150,RMVar_hsa_circ_273625,RMVar_hsa_circ_285071,RMVar_hsa_circ_211148,RMVar_hsa_circ_281693,RMVar_hsa_circ_211151,RMVar_hsa_circ_211149 83353 RMVar_ID_83353 Human_SNP_ID_686601631 m1A Human chr20 - 62126334 62126334 62126334 TCGGAAAGGGCTGTAAGGCACGTGCGGCTGGAAGGGCGAGGCGGAGGCAGAACCCAGGGAAGACT TCGGAAAGGGCTGTAAGGCACGTGCGGCTGGACGGGCGAGGCGGAGGCAGAACCCAGGGAAGACT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62126293..62126398 26863196 MeRIP-seq:(Medium) rs1050637536 Functional Loss SNV dbSNP153 33..33 33 - - - 83354 RMVar_ID_83354 Human_SNP_ID_686603326 m1A Human chr20 - 62132165 62132165 62132165 TCCCATCGCCCTCACTGCCTGGCCTTCACGACATGCTGTTCTATTTTTCCCCTGGCAGAACATGA TCCCATCGCCCTCACTGCCTGGCCTTCACGACCTGCTGTTCTATTTTTCCCCTGGCAGAACATGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62132161..62132774 26863196 MeRIP-seq:(Medium) rs1205592071 Functional Loss SNV dbSNP153 33..33 33 - - - 83355 RMVar_ID_83355 Human_SNP_ID_686603644 m1A Human chr20 - 62133377 62133377 62133377 CCATTGCCCCTGCCTCCTCGGAATCCGCCCCGAGAACTGCGGCCACGAAGAAACCTCCCTGACAC CCATTGCCCCTGCCTCCTCGGAATCCGCCCCGGGAACTGCGGCCACGAAGAAACCTCCCTGACAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62133326..62133522 26863196 MeRIP-seq:(Medium) rs770018797 Functional Loss SNV dbSNP153 33..33 33 - - - 83356 RMVar_ID_83356 Human_SNP_ID_686603645 m1A Human chr20 - 62133377 62133377 62133377 CCATTGCCCCTGCCTCCTCGGAATCCGCCCCGAGAACTGCGGCCACGAAGAAACCTCCCTGACAC CCATTGCCCCTGCCTCCTCGGAATCCGCCCCGCGAACTGCGGCCACGAAGAAACCTCCCTGACAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62133326..62133522 26863196 MeRIP-seq:(Medium) rs770018797 Functional Loss SNV dbSNP153 33..33 33 - - - 83357 RMVar_ID_83357 Human_SNP_ID_686603658 m1A Human chr20 + 62133399 62133399 62133399 GCCGCAGTTCTCGGGGCGGATTCCGAGGAGGCAGGGGCAATGGGACCACCCGTCGCAACCCCACT GCCGCAGTTCTCGGGGCGGATTCCGAGGAGGCGGGGGCAATGGGACCACCCGTCGCAACCCCACT A G LSM14B Ensembl:ENSG00000149657 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62133348..62133523 26863196 MeRIP-seq:(Medium) rs546418770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_567983,Human_RBP_ID_7018675,Human_RBP_ID_18776474,Human_RBP_ID_23004888 Human_Splice_Rec_2100719 83358 RMVar_ID_83358 Human_SNP_ID_686604114 m1A Human chr20 + 62134769 62134769 62134769 CATCCACAGTGATGTCAAGGTTGGGGCTGGCCAGGGGTGGGTGGACTAGAAGCATTTGGGAGTAG CATCCACAGTGATGTCAAGGTTGGGGCTGGCCGGGGGTGGGTGGACTAGAAGCATTTGGGAGTAG A G LSM14B Ensembl:ENSG00000149657 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62134718..62134832 26863196 MeRIP-seq:(Medium) rs539806848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5089255,Human_RBP_ID_5148223,Human_RBP_ID_5529200,Human_RBP_ID_7018692,Human_RBP_ID_8204159,Human_RBP_ID_9431364,Human_RBP_ID_17975345,Human_RBP_ID_21983067,Human_RBP_ID_22371404,Human_RBP_ID_22478894,Human_RBP_ID_23004228,Human_RBP_ID_26493207 Human_miRNA_ID_960628,Human_miRNA_ID_1811358 83359 RMVar_ID_83359 Human_SNP_ID_686604171 m1A Human chr20 - 62134951 62134951 62134951 GAACGCCAGTGTGTGGCCAGAGTCCAGCAATGACTGACCGGCCCAGGTCAGAGGCTGGCAGGGAC GAACGCCAGTGTGTGGCCAGAGTCCAGCAATGGCTGACCGGCCCAGGTCAGAGGCTGGCAGGGAC T C lnc-PSMA7-1 RNACentral:URS00008B7B44 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:62134901..62134975 32194978 MeRIP-seq:(Medium) rs1259546900 Functional Loss SNV dbSNP153 33..33 33 - - - 83360 RMVar_ID_83360 Human_SNP_ID_686606136 m1A Human chr20 - 62140933 62140933 62140933 GTTTGTGGATCTTAATTAAAGGTTGGTGTTCGAGGAAGAGACATTGTTGTTCTTGGTGTGGAGAA GTTTGTGGATCTTAATTAAAGGTTGGTGTTCGTGGAAGAGACATTGTTGTTCTTGGTGTGGAGAA T A PSMA7 Ensembl:ENSG00000101182 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62140771..62140994 26863196 MeRIP-seq:(Medium) rs748876751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62354,Human_RBP_ID_568059,Human_RBP_ID_778675,Human_RBP_ID_1600102,Human_RBP_ID_1932497,Human_RBP_ID_4659963,Human_RBP_ID_9389639,Human_RBP_ID_14160807,Human_RBP_ID_17975357,Human_RBP_ID_22453600 Human_Splice_Rec_2100754,Human_Splice_Rec_2100774,Human_Splice_Rec_2100786,Human_Splice_Rec_2100804 RMVar_hsa_circ_211154,RMVar_hsa_circ_122126,RMVar_hsa_circ_211157,RMVar_hsa_circ_291342,RMVar_hsa_circ_211158,RMVar_hsa_circ_372377,RMVar_hsa_circ_270124,RMVar_hsa_circ_211160,RMVar_hsa_circ_325002,RMVar_hsa_circ_211159,RMVar_hsa_circ_299953,RMVar_hsa_circ_81727,RMVar_hsa_circ_211161 83361 RMVar_ID_83361 Human_SNP_ID_686606905 m1A Human chr20 - 62143296 62143296 62143296 AGGAGCCCGGCCGCCGCCCGCCGGCATGAGCTACGACCGCGCCATCACCGTCTTCTCGCCCGACG AGGAGCCCGGCCGCCGCCCGCCGGCATGAGCTTCGACCGCGCCATCACCGTCTTCTCGCCCGACG T A PSMA7 Ensembl:ENSG00000101182 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62143276..62143300 26863196 MeRIP-seq:(Medium) rs1200708104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62355,Human_RBP_ID_244233,Human_RBP_ID_778678,Human_RBP_ID_1600105,Human_RBP_ID_1932500,Human_RBP_ID_4655543,Human_RBP_ID_5503648,Human_RBP_ID_9331630,Human_RBP_ID_18209369,Human_RBP_ID_18776507,Human_RBP_ID_22453155,Human_RBP_ID_27023745,Human_RBP_ID_27487879 Human_Splice_Rec_2100753,Human_Splice_Rec_2100773,Human_Splice_Rec_2100803 Human_miRNA_ID_2975902 RMVar_hsa_circ_211154,RMVar_hsa_circ_122126 83362 RMVar_ID_83362 Human_SNP_ID_686606906 m1A Human chr20 - 62143296 62143296 62143296 AGGAGCCCGGCCGCCGCCCGCCGGCATGAGCTACGACCGCGCCATCACCGTCTTCTCGCCCGACG AGGAGCCCGGCCGCCGCCCGCCGGCATGAGCTGCGACCGCGCCATCACCGTCTTCTCGCCCGACG T C PSMA7 Ensembl:ENSG00000101182 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62143276..62143300 26863196 MeRIP-seq:(Medium) rs1200708104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62355,Human_RBP_ID_244233,Human_RBP_ID_778678,Human_RBP_ID_1600105,Human_RBP_ID_1932500,Human_RBP_ID_4655543,Human_RBP_ID_5503648,Human_RBP_ID_9331630,Human_RBP_ID_18209369,Human_RBP_ID_18776507,Human_RBP_ID_22453155,Human_RBP_ID_27023745,Human_RBP_ID_27487879 Human_Splice_Rec_2100753,Human_Splice_Rec_2100773,Human_Splice_Rec_2100803 Human_miRNA_ID_2975902 RMVar_hsa_circ_211154,RMVar_hsa_circ_122126 83363 RMVar_ID_83363 Human_SNP_ID_686606934 m1A Human chr20 - 62143329 62143329 62143329 CCGTGAGTGTGCGCTTTTGAGAGTCGCGGCGGAAGGAGCCCGGCCGCCGCCCGCCGGCATGAGCT CCGTGAGTGTGCGCTTTTGAGAGTCGCGGCGGTAGGAGCCCGGCCGCCGCCCGCCGGCATGAGCT T A PSMA7 Ensembl:ENSG00000101182 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:62142877..62143475;chr20:62143136..62143475 26863196 MeRIP-seq:(Medium) rs1201103595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244233,Human_RBP_ID_778678,Human_RBP_ID_1600106,Human_RBP_ID_4659510,Human_RBP_ID_9118899,Human_RBP_ID_17975359,Human_RBP_ID_18193687,Human_RBP_ID_22453155,Human_RBP_ID_23212505,Human_RBP_ID_23914878 RMVar_hsa_circ_211154,RMVar_hsa_circ_122126 83364 RMVar_ID_83364 Human_SNP_ID_686606966 m1A Human chr20 + 62143378 62143378 62143378 AAGCGCACACTCACGGCCCGCGCGCACCCGCGACTCCCGGCGCCACTACGCCCGCGCCCCACCCT AAGCGCACACTCACGGCCCGCGCGCACCCGCGTCTCCCGGCGCCACTACGCCCGCGCCCCACCCT A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr20:62143283..62143408;chr20:62143283..62143440 26863196,26863410 MeRIP-seq:(Medium) rs1189498118 Functional Loss SNV dbSNP153 33..33 33 - - - 83365 RMVar_ID_83365 Human_SNP_ID_686608420 m1A Human chr20 - 62147101 62147101 62147101 CTGCCCCTGCCCCATGGTTCTCTTTCTCTGGGATAGCCCTCACCACAAACGCACTCTCGTGGGCT CTGCCCCTGCCCCATGGTTCTCTTTCTCTGGGGTAGCCCTCACCACAAACGCACTCTCGTGGGCT T C HSALNG0131485 RNACentral:URS0000E9F7CC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62147095..62147259 26863196 MeRIP-seq:(Medium) rs1476564458 Functional Loss SNV dbSNP153 33..33 33 - - - 83366 RMVar_ID_83366 Human_SNP_ID_686609888 m1A Human chr20 + 62151757 62151757 62151757 GTCTCTGCAGTGAGCACAGGCTTTGGTTGAGAAAGTCACCCCCACAATGGGCACAGGACTCCTGT GTCTCTGCAGTGAGCACAGGCTTTGGTTGAGAGAGTCACCCCCACAATGGGCACAGGACTCCTGT A G SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62151755..62152099 26863196 MeRIP-seq:(Medium) rs918365140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77527,RMVar_hsa_circ_211162 83367 RMVar_ID_83367 Human_SNP_ID_686609910 m1A Human chr20 - 62151814 62151813 62151815 AACGGGGGAGGCCAGCTATGGGGAGCGGGAAAAGAGGGGAACGGGGGCTGCTGGGGGACAGGAGT AACGGGGGAGGCCAGCTATGGGGAGCGGGAA__GAGGGGAACGGGGGCTGCTGGGGGACAGGAGT CTT C HSALNG0131485 RNACentral:URS0000E9F7CC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:62151811..62152119;chr20:62151805..62151893 26863196 MeRIP-seq:(Medium) rs1397329495 Functional Loss DEL dbSNP153 32..33 33 - - - 83368 RMVar_ID_83368 Human_SNP_ID_686610383 m1A Human chr20 + 62153029 62153029 62153029 AAATATCTGAGATGGGGTAATTTATAAAGGAAAGAGGCTTAATTAACTCACAGTTCCACAGGGCT AAATATCTGAGATGGGGTAATTTATAAAGGAAGGAGGCTTAATTAACTCACAGTTCCACAGGGCT A G SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62153024..62153148 26863196 MeRIP-seq:(Medium) rs1255842551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77527,RMVar_hsa_circ_211162 83369 RMVar_ID_83369 Human_SNP_ID_686612691 m1A Human chr20 + 62160143 62160143 62160143 CGGTGGTGACCAACCCTTCCTGACAGACTGGGAGTAATGACAGCGTCTGAGGTGGCCAGGTCAGA CGGTGGTGACCAACCCTTCCTGACAGACTGGGCGTAATGACAGCGTCTGAGGTGGCCAGGTCAGA A C SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62160037..62160254 26863196 MeRIP-seq:(Medium) rs1324495871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264555,Human_RBP_ID_924136,Human_RBP_ID_3654431,Human_RBP_ID_5385520,Human_RBP_ID_8113572,Human_RBP_ID_8204171,Human_RBP_ID_9431125,Human_RBP_ID_14160985,Human_RBP_ID_18950859,Human_RBP_ID_19004491,Human_RBP_ID_19110075,Human_RBP_ID_26770655 RMVar_hsa_circ_21003,RMVar_hsa_circ_334669,RMVar_hsa_circ_211164,RMVar_hsa_circ_211165,RMVar_hsa_circ_336781,RMVar_hsa_circ_377144 83370 RMVar_ID_83370 Human_SNP_ID_686612858 m1A Human chr20 - 62160445 62160445 62160445 GTGCACGGTTCACAGTGGCTCAAAGCACCCGGAGAGGCTCCAGGGAGACGCAGGGCCCCCATCCC GTGCACGGTTCACAGTGGCTCAAAGCACCCGGTGAGGCTCCAGGGAGACGCAGGGCCCCCATCCC T A lnc-PSMA7-2 RNACentral:URS00008BA57E lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62160397..62160581 26863196 MeRIP-seq:(Medium) rs1319457759 Functional Loss SNV dbSNP153 33..33 33 - - - 83371 RMVar_ID_83371 Human_SNP_ID_686613064 m1A Human chr20 - 62161066 62161066 62161066 GGCGCAGGTGACCAGCGCCTCTGTGCTCCCCAACCACGACCCCTCCGTGCCAAGAGCTTCGGCAG GGCGCAGGTGACCAGCGCCTCTGTGCTCCCCAGCCACGACCCCTCCGTGCCAAGAGCTTCGGCAG T C lnc-PSMA7-2 RNACentral:URS00008BA57E lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62161022..62161106 26863196 MeRIP-seq:(Medium) rs1003367247 Functional Loss SNV dbSNP153 33..33 33 - - - 83372 RMVar_ID_83372 Human_SNP_ID_686614727 m1A Human chr20 + 62165544 62165528 62165544 GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGAGCGTAAGCGCCACACGCAGCAGAGTTAAGACG GGGGTAAGGAGCACGGC________________GCGTAAGCGCCACACGCAGCAGAGTTAAGACG CTGCGTGCTGGGCTCGA C SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62165534..62165605 26863196 MeRIP-seq:(Medium) rs1568755607 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_19006129,Human_RBP_ID_19106926 RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 83373 RMVar_ID_83373 Human_SNP_ID_686614729 m1A Human chr20 + 62165544 62165529 62165544 GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGAGCGTAAGCGCCACACGCAGCAGAGTTAAGACG GGGGTAAGGAGCACGGCT_______________GCGTAAGCGCCACACGCAGCAGAGTTAAGACG TGCGTGCTGGGCTCGA T SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62165534..62165605 26863196 MeRIP-seq:(Medium) rs540023118 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_19006129,Human_RBP_ID_19106926 RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 83374 RMVar_ID_83374 Human_SNP_ID_686614732 m1A Human chr20 + 62165544 62165531 62165544 GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGAGCGTAAGCGCCACACGCAGCAGAGTTAAGACG GGGGTAAGGAGCACGGCTGC_____________GCGTAAGCGCCACACGCAGCAGAGTTAAGACG CGTGCTGGGCTCGA C SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62165534..62165605 26863196 MeRIP-seq:(Medium) rs60342665 Functional Loss DEL dbSNP153,HGVD 21..33 33 - - - Human_RBP_ID_19006129,Human_RBP_ID_19106926 RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 83375 RMVar_ID_83375 Human_SNP_ID_686614749 m1A Human chr20 + 62165544 62165544 62165544 GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGAGCGTAAGCGCCACACGCAGCAGAGTTAAGACG GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGCGCGTAAGCGCCACACGCAGCAGAGTTAAGACG A C SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62165534..62165605 26863196 MeRIP-seq:(Medium) rs201669693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19006129,Human_RBP_ID_19106926 RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 83376 RMVar_ID_83376 Human_SNP_ID_686615913 m1A Human chr20 + 62168952 62168952 62168952 GAATCTGATAAAACGAGAGGGTGTTCATGCGCAGGGCACCAGTAATAGGAGGGGACCAGAGTGGG GAATCTGATAAAACGAGAGGGTGTTCATGCGCGGGGCACCAGTAATAGGAGGGGACCAGAGTGGG A G SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:62168950..62169089;chr20:62168950..62169055 26863196 MeRIP-seq:(Medium) rs1177017004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 83377 RMVar_ID_83377 Human_SNP_ID_686620128 m1A Human chr20 - 62182793 62182793 62182793 ACAGCCGCCCCGCCCGTTCCACCCGGTGCCCAAGGTCCCCCAGCTTCTCTGACCCCTCCGGCGTT ACAGCCGCCCCGCCCGTTCCACCCGGTGCCCAGGGTCCCCCAGCTTCTCTGACCCCTCCGGCGTT T C lnc-HRH3-3,lnc-HRH3-3:2,lnc-HRH3-3:3 RNACentral:URS0000D59A75,RNACentral:URS0000D585BB,RNACentral:URS0000D5DC60 lincRNA,lincRNA,lincRNA exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62182785..62182911 26863196 MeRIP-seq:(Medium) rs553100590 Functional Loss SNV dbSNP153 33..33 33 - - - 83378 RMVar_ID_83378 Human_SNP_ID_686620129 m1A Human chr20 - 62182793 62182793 62182793 ACAGCCGCCCCGCCCGTTCCACCCGGTGCCCAAGGTCCCCCAGCTTCTCTGACCCCTCCGGCGTT ACAGCCGCCCCGCCCGTTCCACCCGGTGCCCACGGTCCCCCAGCTTCTCTGACCCCTCCGGCGTT T G lnc-HRH3-3,lnc-HRH3-3:2,lnc-HRH3-3:3 RNACentral:URS0000D59A75,RNACentral:URS0000D585BB,RNACentral:URS0000D5DC60 lincRNA,lincRNA,lincRNA exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62182785..62182911 26863196 MeRIP-seq:(Medium) rs553100590 Functional Loss SNV dbSNP153 33..33 33 - - - 83379 RMVar_ID_83379 Human_SNP_ID_686620292 m1A Human chr20 - 62183093 62183091 62183093 CCCTCCTTGCGCCCGGGCCGCGACCACCCCCCAGGCCCACGCTCCCCGCTCCCCGCTCCCGCACT CCCTCCTTGCGCCCGGGCCGCGACCACCCCCC__GCCCACGCTCCCCGCTCCCCGCTCCCGCACT CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62183091..62183281 26863196 MeRIP-seq:(Medium) rs1568777884 Functional Loss DEL dbSNP153 33..34 33 - - - 83380 RMVar_ID_83380 Human_SNP_ID_686620294 m1A Human chr20 - 62183093 62183093 62183093 CCCTCCTTGCGCCCGGGCCGCGACCACCCCCCAGGCCCACGCTCCCCGCTCCCCGCTCCCGCACT CCCTCCTTGCGCCCGGGCCGCGACCACCCCCCCGGCCCACGCTCCCCGCTCCCCGCTCCCGCACT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62183091..62183281 26863196 MeRIP-seq:(Medium) rs1425715824 Functional Loss SNV dbSNP153 33..33 33 - - - 83381 RMVar_ID_83381 Human_SNP_ID_686620411 m1A Human chr20 - 62183338 62183338 62183338 CGTGACAGAGCACCACCGGGGTGGCTGACAAGACTTCTGACCCCAAAACGCGGTTCTGCGGAGAG CGTGACAGAGCACCACCGGGGTGGCTGACAAGCCTTCTGACCCCAAAACGCGGTTCTGCGGAGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62183297..62183403 32194978 MeRIP-seq:(Medium) rs1034925310 Functional Loss SNV dbSNP153 33..33 33 - - - 83382 RMVar_ID_83382 Human_SNP_ID_686624796 m1A Human chr20 - 62197901 62197901 62197901 CAGTTTTTACTCCCTCCATCTTCTCCACTGAAACCCTGGTACCGCGACAGGACCGACGACAGGGA CAGTTTTTACTCCCTCCATCTTCTCCACTGAAGCCCTGGTACCGCGACAGGACCGACGACAGGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62197848..62197965 26863196 MeRIP-seq:(Medium) rs1485833504 Functional Loss SNV dbSNP153 33..33 33 - - - 83383 RMVar_ID_83383 Human_SNP_ID_686626033 m1A Human chr20 + 62201388 62201388 62201388 TGCCCATAACGGGGTGGCCCTGCCGCTGACTCAGGTCTCCGCCATGCACGCGTGGACTCTCGGAT TGCCCATAACGGGGTGGCCCTGCCGCTGACTCGGGTCTCCGCCATGCACGCGTGGACTCTCGGAT A G MTG2 Ensembl:ENSG00000101181 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2151511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26492364 GWAS_ID_10079,GWAS_ID_10080,GWAS_ID_10081,GWAS_ID_10082,GWAS_ID_10083 83384 RMVar_ID_83384 Human_SNP_ID_686626607 m1A Human chr20 + 62203312 62203312 62203312 GTCCTTTGCTGAAGCTGAGGCTCCAGAGGGGGAGTCACTGCCACGAAGGTTGCCCAGAACTTTCC GTCCTTTGCTGAAGCTGAGGCTCCAGAGGGGGGGTCACTGCCACGAAGGTTGCCCAGAACTTTCC A G MTG2 Ensembl:ENSG00000101181 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62203174..62203323 32194978 MeRIP-seq:(Medium) rs1420412376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3652970,Human_RBP_ID_26493728,Human_RBP_ID_27299238 83385 RMVar_ID_83385 Human_SNP_ID_686651423 m1A Human chr20 - 62288423 62288422 62288423 CAGCCTCCCAGCCTCTGCACCCATAGCCTCCCAGCCTCTGCACCCACAGCCTCCCAGCCTCTGCA CAGCCTCCCAGCCTCTGCACCCATAGCCTCCC_GCCTCTGCACCCACAGCCTCCCAGCCTCTGCA CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62288417..62288488 26863196 MeRIP-seq:(Medium) rs1210769684 Functional Loss DEL dbSNP153 33..33 33 - - - 83386 RMVar_ID_83386 Human_SNP_ID_686651425 m1A Human chr20 - 62288423 62288423 62288423 CAGCCTCCCAGCCTCTGCACCCATAGCCTCCCAGCCTCTGCACCCACAGCCTCCCAGCCTCTGCA CAGCCTCCCAGCCTCTGCACCCATAGCCTCCCGGCCTCTGCACCCACAGCCTCCCAGCCTCTGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62288417..62288488 26863196 MeRIP-seq:(Medium) rs1481687423 Functional Loss SNV dbSNP153 33..33 33 - - - 83387 RMVar_ID_83387 Human_SNP_ID_686652404 m1A Human chr20 + 62291775 62291775 62291775 GAGAGAAGCACGGAGGGAGCGGGCCAAGGAGGAGGCAGAGTGGCAGACGAGGTGAGTACTGTGGT GAGAGAAGCACGGAGGGAGCGGGCCAAGGAGGCGGCAGAGTGGCAGACGAGGTGAGTACTGTGGT A C OSBPL2 Ensembl:ENSG00000130703 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62291660..62291856 26863196 MeRIP-seq:(Medium) rs560977879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9389651,Human_RBP_ID_19006143,Human_RBP_ID_24546881,Human_RBP_ID_26343186,Human_RBP_ID_27820469 Human_Splice_Rec_2100972,Human_Splice_Rec_2100973,Human_Splice_Rec_2101000,Human_Splice_Rec_2101001,Human_Splice_Rec_2101038,Human_Splice_Rec_2101039,Human_Splice_Rec_2101064,Human_Splice_Rec_2101065,Human_Splice_Rec_2101088,Human_Splice_Rec_2101089,Human_Splice_Rec_2101114,Human_Splice_Rec_2101115,Human_Splice_Rec_2101144,Human_Splice_Rec_2101145,Human_Splice_Rec_2101168,Human_Splice_Rec_2101169,Human_Splice_Rec_2101196,Human_Splice_Rec_2101197,Human_Splice_Rec_2101218,Human_Splice_Rec_2101219,Human_Splice_Rec_2101250,Human_Splice_Rec_2101251,Human_Splice_Rec_2101270,Human_Splice_Rec_2101271,Human_Splice_Rec_2101292,Human_Splice_Rec_2101293,Human_Splice_Rec_2101316,Human_Splice_Rec_2101317,Human_Splice_Rec_2101340,Human_Splice_Rec_2101341,Human_Splice_Rec_2101382,Human_Splice_Rec_2101383,Human_Splice_Rec_2101406,Human_Splice_Rec_2101407,Human_Splice_Rec_2101427 RMVar_hsa_circ_117547,RMVar_hsa_circ_211176,RMVar_hsa_circ_80889,RMVar_hsa_circ_211178,RMVar_hsa_circ_88991,RMVar_hsa_circ_211183,RMVar_hsa_circ_20315,RMVar_hsa_circ_211185,RMVar_hsa_circ_74283,RMVar_hsa_circ_316799,RMVar_hsa_circ_211187,RMVar_hsa_circ_315672 83388 RMVar_ID_83388 Human_SNP_ID_686652415 m1A Human chr20 - 62291795 62291795 62291795 CTGCCCCAGCCTGCGTGGCTACCACAGTACTCACCTCGTCTGCCACTCTGCCTCCTCCTTGGCCC CTGCCCCAGCCTGCGTGGCTACCACAGTACTCCCCTCGTCTGCCACTCTGCCTCCTCCTTGGCCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:62291751..62291800 32194978 MeRIP-seq:(Medium) rs917860058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1241830 83389 RMVar_ID_83389 Human_SNP_ID_686655395 m1A Human chr20 - 62302478 62302478 62302478 GCGGGAGCTGGAGTCCACGCGTCCGGGAGAGCAGGGGTCCGGGAGGGTAGAGCGAGGGTGAGAAC GCGGGAGCTGGAGTCCACGCGTCCGGGAGAGCGGGGGTCCGGGAGGGTAGAGCGAGGGTGAGAAC T C lnc-LAMA5-3 RNACentral:URS0000D5A901 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62302466..62302568 26863196 MeRIP-seq:(Medium) rs927451754 Functional Loss SNV dbSNP153 33..33 33 - - - 83390 RMVar_ID_83390 Human_SNP_ID_686655584 m1A Human chr20 - 62303025 62303025 62303025 TCCCGCACCTGCCTCGCGCCCACACTCGTTCGAGAGGCGCCGTCCGGGCTCGCTCTTCCTCCTCG TCCCGCACCTGCCTCGCGCCCACACTCGTTCGGGAGGCGCCGTCCGGGCTCGCTCTTCCTCCTCG T C lnc-LAMA5-3 RNACentral:URS0000D5A901 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62302951..62303146 26863196 MeRIP-seq:(Medium) rs538006763 Functional Loss SNV dbSNP153 33..33 33 - - - 83391 RMVar_ID_83391 Human_SNP_ID_686655597 m1A Human chr20 + 62303044 62303044 62303044 CGGACGGCGCCTCTCGAACGAGTGTGGGCGCGAGGCAGGTGCGGGAGTCGCCGGGCCTGGGGCGG CGGACGGCGCCTCTCGAACGAGTGTGGGCGCGGGGCAGGTGCGGGAGTCGCCGGGCCTGGGGCGG A G ADRM1 Ensembl:ENSG00000130706 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr20:62302951..62303199;chr20:62302951..62303162;chr20:62302976..62303050 26863196,32194978 MeRIP-seq:(Medium) rs1473473268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659512,Human_RBP_ID_23915159 Human_Splice_Rec_2101431,Human_Splice_Rec_2101449,Human_Splice_Rec_2101465 RMVar_hsa_circ_111727,RMVar_hsa_circ_211190 83392 RMVar_ID_83392 Human_SNP_ID_686656741 m1A Human chr20 + 62306179 62306179 62306179 CTGGGTGAGCTGGCGCCAGCTCCTGCCCTTACATGCCCTTCCTCTTGCAGGAACCCAAGACAGAC CTGGGTGAGCTGGCGCCAGCTCCTGCCCTTACGTGCCCTTCCTCTTGCAGGAACCCAAGACAGAC A G ADRM1 Ensembl:ENSG00000130706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62306176..62306325 26863196 MeRIP-seq:(Medium) rs373438307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22549453,Human_RBP_ID_22601516,Human_RBP_ID_22671090 RMVar_hsa_circ_101576,RMVar_hsa_circ_111727,RMVar_hsa_circ_211190,RMVar_hsa_circ_211191 83393 RMVar_ID_83393 Human_SNP_ID_686656742 m1A Human chr20 - 62306180 62306180 62306180 GGTCTGTCTTGGGTTCCTGCAAGAGGAAGGGCATGTAAGGGCAGGAGCTGGCGCCAGCTCACCCA GGTCTGTCTTGGGTTCCTGCAAGAGGAAGGGCGTGTAAGGGCAGGAGCTGGCGCCAGCTCACCCA T C AL354836.1 Ensembl:ENSG00000226332 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62306176..62306275 26863196 MeRIP-seq:(Medium) rs760800805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926408,Human_RBP_ID_5595445 83394 RMVar_ID_83394 Human_SNP_ID_686657385 m1A Human chr20 - 62307627 62307627 62307627 TGGGGTGGCACGGGTGGAAGAGGTGGTGGATGACGGGGTGACCGCTGCCGACTGGCTCCGGGAGC TGGGGTGGCACGGGTGGAAGAGGTGGTGGATGGCGGGGTGACCGCTGCCGACTGGCTCCGGGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62307326..62307850 26863196 MeRIP-seq:(Medium) rs1020715949 Functional Loss SNV dbSNP153 33..33 33 - - - 83395 RMVar_ID_83395 Human_SNP_ID_686657794 m1A Human chr20 + 62308442 62308442 62308442 GGCCCCCTCATGTGCCAGTTCGGTCTGCCTGCAGAGGCTGTGGAGGCCGCCAACAAGGGCGGTAA GGCCCCCTCATGTGCCAGTTCGGTCTGCCTGCGGAGGCTGTGGAGGCCGCCAACAAGGGCGGTAA A G ADRM1 Ensembl:ENSG00000130706 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62306176..62308910 32194978 MeRIP-seq:(Medium) rs1275696467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244489,Human_RBP_ID_1600166,Human_RBP_ID_3960368,Human_RBP_ID_5383106,Human_RBP_ID_19004503,Human_RBP_ID_22452816,Human_RBP_ID_23915169,Human_RBP_ID_27159028 Human_Splice_Rec_2101446,Human_Splice_Rec_2101447,Human_Splice_Rec_2101462,Human_Splice_Rec_2101463,Human_Splice_Rec_2101480,Human_Splice_Rec_2101481 RMVar_hsa_circ_101576,RMVar_hsa_circ_111727,RMVar_hsa_circ_211190,RMVar_hsa_circ_211191,RMVar_hsa_circ_94931,RMVar_hsa_circ_211197,RMVar_hsa_circ_87881,RMVar_hsa_circ_103573,RMVar_hsa_circ_211199,RMVar_hsa_circ_97223,RMVar_hsa_circ_211200,RMVar_hsa_circ_211201 83396 RMVar_ID_83396 Human_SNP_ID_686657935 m1A Human chr20 + 62308721 62308713 62308722 CGCCAAGCCCGAGCAGAAAGAGGGCGACACGAAGGACAAGAAGGACGAAGAGGAGGACATGAGCC CGCCAAGCCCGAGCAGAAAGAGGGC_________GACAAGAAGGACGAAGAGGAGGACATGAGCC CGACACGAAG C ADRM1 Ensembl:ENSG00000130706 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62308642..62308811 26863196 MeRIP-seq:(Medium) rs202079747 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_1600167,Human_RBP_ID_1932563,Human_RBP_ID_5597075,Human_RBP_ID_27489065 Human_Splice_Rec_2101448,Human_Splice_Rec_2101464,Human_Splice_Rec_2101482 Human_miRNA_ID_2255769 RMVar_hsa_circ_101576,RMVar_hsa_circ_111727,RMVar_hsa_circ_211190,RMVar_hsa_circ_211191,RMVar_hsa_circ_94931,RMVar_hsa_circ_211197,RMVar_hsa_circ_87881,RMVar_hsa_circ_103573,RMVar_hsa_circ_211199,RMVar_hsa_circ_97223,RMVar_hsa_circ_211200,RMVar_hsa_circ_211201 83397 RMVar_ID_83397 Human_SNP_ID_686658270 m1A Human chr20 - 62309345 62309345 62309345 GTCCACGGGGCAGTGGGGGCCAGTGGCTGCCCAGCCGCCTAGGACACAGCCAACCCCGGCCCCTG GTCCACGGGGCAGTGGGGGCCAGTGGCTGCCCCGCCGCCTAGGACACAGCCAACCCCGGCCCCTG T G LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62309295..62309415 26863196 MeRIP-seq:(Medium) rs1282080576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119055,Human_RBP_ID_5472291,Human_RBP_ID_17659091,Human_RBP_ID_22767410 83398 RMVar_ID_83398 Human_SNP_ID_686658287 m1A Human chr20 - 62309366 62309366 62309366 GCCATGACTCGCTCTGTGGAGGTCCACGGGGCAGTGGGGGCCAGTGGCTGCCCAGCCGCCTAGGA GCCATGACTCGCTCTGTGGAGGTCCACGGGGCGGTGGGGGCCAGTGGCTGCCCAGCCGCCTAGGA T C LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62309351..62309375 26863196 MeRIP-seq:(Medium) rs897320081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119055,Human_RBP_ID_5472291,Human_RBP_ID_17659091,Human_RBP_ID_22767410 83399 RMVar_ID_83399 Human_SNP_ID_686659079 m1A Human chr20 - 62310545 62310545 62310545 TATAGGTGACCGTCGGGTTCAGCGGCTGTGTGAAGAGACTGAGGCTGCACGGGAGGCCCCTGGGG TATAGGTGACCGTCGGGTTCAGCGGCTGTGTGGAGAGACTGAGGCTGCACGGGAGGCCCCTGGGG T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62310392..62310564 26863196 MeRIP-seq:(Medium) rs78109712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62865,Human_RBP_ID_5119418,Human_RBP_ID_5529205,Human_RBP_ID_18167729,Human_RBP_ID_18471157,Human_RBP_ID_19006154,Human_RBP_ID_23258208 Human_Splice_Rec_2101674 RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203 83400 RMVar_ID_83400 Human_SNP_ID_686659350 m1A Human chr20 - 62311027 62311027 62311027 CCCGAGGCCTCCTCCTCTTCACTGCCCGTCTGAGGCCCGGCAGCCCCTCCCTGGCGCTCTTCCTG CCCGAGGCCTCCTCCTCTTCACTGCCCGTCTGTGGCCCGGCAGCCCCTCCCTGGCGCTCTTCCTG T A LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62310976..62311100 26863196 MeRIP-seq:(Medium) rs762191283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779030,Human_RBP_ID_4655844 Human_Splice_Rec_2101516,Human_Splice_Rec_2101670 Human_miRNA_ID_2391390,Human_miRNA_ID_2592636,Human_miRNA_ID_2691243,Human_miRNA_ID_2694577 RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_365302,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_310338,RMVar_hsa_circ_211205 83401 RMVar_ID_83401 Human_SNP_ID_686659495 m1A Human chr20 + 62311272 62311272 62311272 GTGGTCCTGAGGTGTGGGGGCAGCATGCAGGCAGGATGCCGGGCGGGCTGACGGCTGCGGCGGGA GTGGTCCTGAGGTGTGGGGGCAGCATGCAGGCTGGATGCCGGGCGGGCTGACGGCTGCGGCGGGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr20:62310676..62311796;chr20:62311067..62311450 26863196 MeRIP-seq:(Medium) rs1568890182 Functional Loss SNV dbSNP153 33..33 33 - - - 83402 RMVar_ID_83402 Human_SNP_ID_686659751 m1A Human chr20 - 62311730 62311730 62311730 CAGCTCCAGCAGATGAAGCCCCACCGGGGACCACCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC CAGCTCCAGCAGATGAAGCCCCACCGGGGACCGCCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC T C LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62311680..62311774 26863196 MeRIP-seq:(Medium) rs1014927606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779031,Human_RBP_ID_18167736 Human_Splice_Rec_2101510,Human_Splice_Rec_2101664,Human_Splice_Rec_2101690 RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_211205 83403 RMVar_ID_83403 Human_SNP_ID_686659752 m1A Human chr20 - 62311730 62311730 62311730 CAGCTCCAGCAGATGAAGCCCCACCGGGGACCACCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC CAGCTCCAGCAGATGAAGCCCCACCGGGGACCCCCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC T G LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62311680..62311774 26863196 MeRIP-seq:(Medium) rs1014927606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779031,Human_RBP_ID_18167736 Human_Splice_Rec_2101510,Human_Splice_Rec_2101664,Human_Splice_Rec_2101690 RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_211205 83404 RMVar_ID_83404 Human_SNP_ID_686660176 m1A Human chr20 + 62312458 62312458 62312458 TCACGCCTGTCGTGTTCAGCCGCTTGAGGTCCACATACTTGCCCAGGGCCTTGATGCCTTTGACG TCACGCCTGTCGTGTTCAGCCGCTTGAGGTCCGCATACTTGCCCAGGGCCTTGATGCCTTTGACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62312399..62312533 26863196 MeRIP-seq:(Medium) rs755292595 Functional Loss SNV dbSNP153 33..33 33 - - - 83405 RMVar_ID_83405 Human_SNP_ID_686660369 m1A Human chr20 - 62312780 62312780 62312780 AGCTGGCCCTGGAGCCCCCACTGGTCCTGTAGATCCAGGTGTTCCTGCTGGGGGGCAGCCGCAAG AGCTGGCCCTGGAGCCCCCACTGGTCCTGTAGGTCCAGGTGTTCCTGCTGGGGGGCAGCCGCAAG T C LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62312768..62312871 26863196 MeRIP-seq:(Medium) rs1387763042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62879,Human_RBP_ID_5385563 Human_Splice_Rec_2101502,Human_Splice_Rec_2101656 RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_211205,RMVar_hsa_circ_26378,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_80201,RMVar_hsa_circ_211210,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211213,RMVar_hsa_circ_94807 83406 RMVar_ID_83406 Human_SNP_ID_686660470 m1A Human chr20 - 62312977 62312977 62312977 GCCAGTTCCTGTGCTTGGCCGTGCAAGAAGGCAGCCTCGTGCTGTTGTATGACTTTGGGGCTGGC GCCAGTTCCTGTGCTTGGCCGTGCAAGAAGGCGGCCTCGTGCTGTTGTATGACTTTGGGGCTGGC T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62312926..62313499 32194978 MeRIP-seq:(Medium) rs1423264080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62880,Human_RBP_ID_5384042,Human_RBP_ID_9389659,Human_RBP_ID_18167746,Human_RBP_ID_19110087,Human_RBP_ID_23212366 Human_Splice_Rec_2101654,Human_Splice_Rec_2101655 RMVar_hsa_circ_127731,RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_211205,RMVar_hsa_circ_26378,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_80201,RMVar_hsa_circ_211210,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211213,RMVar_hsa_circ_94807,RMVar_hsa_circ_320648,RMVar_hsa_circ_211214,RMVar_hsa_circ_211215 83407 RMVar_ID_83407 Human_SNP_ID_686660846 m1A Human chr20 - 62313718 62313718 62313718 GAAACCAAGGGTGACACGGTGGCCCCTGGGGCAGAGGGGCTGCTCAACCTGCGGCCAGACGACTT GAAACCAAGGGTGACACGGTGGCCCCTGGGGCCGAGGGGCTGCTCAACCTGCGGCCAGACGACTT T G LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62313628..62313829 26863196 MeRIP-seq:(Medium) rs781109539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62883 Human_Splice_Rec_2101496,Human_Splice_Rec_2101497,Human_Splice_Rec_2101648,Human_Splice_Rec_2101649 RMVar_hsa_circ_127731,RMVar_hsa_circ_51024,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218 83408 RMVar_ID_83408 Human_SNP_ID_686660953 m1A Human chr20 + 62313923 62313921 62313923 ACGGAGAGATGAGGGGTGGCGAGTGGGCACGGAGAGACGAGGGGTGGCGAGTGGGCATGGAGAGA ACGGAGAGATGAGGGGTGGCGAGTGGGCACG__GAGACGAGGGGTGGCGAGTGGGCATGGAGAGA GGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62313919..62314064 26863196 MeRIP-seq:(Medium) rs1167822625 Functional Loss DEL dbSNP153 32..33 33 - - - 83409 RMVar_ID_83409 Human_SNP_ID_686661272 m1A Human chr20 + 62314375 62314375 62314375 TCATCGATGCTTAGGACTGCAGGGCCCGCCTCACCCAGCTGATACACCCAGTGCACCTTCTTGTC TCATCGATGCTTAGGACTGCAGGGCCCGCCTCCCCCAGCTGATACACCCAGTGCACCTTCTTGTC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62314326..62314425 26863196 MeRIP-seq:(Medium) rs1568899217 Functional Loss SNV dbSNP153 33..33 33 - - - 83410 RMVar_ID_83410 Human_SNP_ID_686661847 m1A Human chr20 + 62315591 62315591 62315591 CCAAGCCTCTCAGGGTGGGAGCCCTGGTCCTCACCGCCCAAGGTCTTGCCAGCCCCTTGGTTCCA CCAAGCCTCTCAGGGTGGGAGCCCTGGTCCTCGCCGCCCAAGGTCTTGCCAGCCCCTTGGTTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62315590..62315661 26863196 MeRIP-seq:(Medium) rs1240078735 Functional Loss SNV dbSNP153 33..33 33 - - - 83411 RMVar_ID_83411 Human_SNP_ID_686662449 m1A Human chr20 - 62316988 62316988 62316988 CATCCTGGACGTCAACCAGGACCGCCTCACCCAGAGGGCCATCGAGGCCTCCAACGCCTACAGCC CATCCTGGACGTCAACCAGGACCGCCTCACCCGGAGGGCCATCGAGGCCTCCAACGCCTACAGCC T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62316940..62317021 26863196 MeRIP-seq:(Medium) rs776082651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62896,Human_RBP_ID_9391106,Human_RBP_ID_23115477 Human_Splice_Rec_2101634 Human_miRNA_ID_2425813,Human_miRNA_ID_2427833,Human_miRNA_ID_2435483 RMVar_hsa_circ_127731,RMVar_hsa_circ_51024,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_26149 83412 RMVar_ID_83412 Human_SNP_ID_686662672 m1A Human chr20 + 62317432 62317429 62317432 CCACTAGACGCAGCTTGCTGCCCGCCGGGGAGAAGGTCTGCATCCTCTGCAGCAGTGGGGTCCGA CCACTAGACGCAGCTTGCTGCCCGCCGGGG___AGGTCTGCATCCTCTGCAGCAGTGGGGTCCGA GAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62317348..62317515 26863196 MeRIP-seq:(Medium) rs1190536191 Functional Loss DEL dbSNP153 31..33 33 - - - 83413 RMVar_ID_83413 Human_SNP_ID_686662673 m1A Human chr20 + 62317432 62317432 62317432 CCACTAGACGCAGCTTGCTGCCCGCCGGGGAGAAGGTCTGCATCCTCTGCAGCAGTGGGGTCCGA CCACTAGACGCAGCTTGCTGCCCGCCGGGGAGGAGGTCTGCATCCTCTGCAGCAGTGGGGTCCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62317348..62317515 26863196 MeRIP-seq:(Medium) rs1568906517 Functional Loss SNV dbSNP153 33..33 33 - - - 83414 RMVar_ID_83414 Human_SNP_ID_686663411 m1A Human chr20 - 62318476 62318476 62318476 ACGGGAGGCCCAGGAGCTCAACAGCCGCAACCAGGAGCGCCTGGAGGAAGCCCTGGTGAGGACCC ACGGGAGGCCCAGGAGCTCAACAGCCGCAACCCGGAGCGCCTGGAGGAAGCCCTGGTGAGGACCC T G LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62318451..62318475 26863196 MeRIP-seq:(Medium) rs1207699472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831852,Human_RBP_ID_19006179 Human_Splice_Rec_2101629 RMVar_hsa_circ_127731,RMVar_hsa_circ_51024,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_26149,RMVar_hsa_circ_265778 83415 RMVar_ID_83415 Human_SNP_ID_686663475 m1A Human chr20 + 62318572 62318572 62318572 GCAGGTCCATGAGGCCGGCCTCGTGCTGGGCCAGCCGGTCGCGGGTTTGTGTGGCCAGTGCCTGG GCAGGTCCATGAGGCCGGCCTCGTGCTGGGCCGGCCGGTCGCGGGTTTGTGTGGCCAGTGCCTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62318521..62318936 26863196 MeRIP-seq:(Medium) rs1368343307 Functional Loss SNV dbSNP153 33..33 33 - - - 83416 RMVar_ID_83416 Human_SNP_ID_686663500 m1A Human chr20 - 62318602 62318599 62318602 GGAGCAGCTGAGCAGCCTCTGGGAGGAGAACCAGGCACTGGCCACACAAACCCGCGACCGGCTGG GGAGCAGCTGAGCAGCCTCTGGGAGGAGAACC___CACTGGCCACACAAACCCGCGACCGGCTGG GCCT G LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62318432..62318688 26863196 MeRIP-seq:(Medium) rs1217019865 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_62900,Human_RBP_ID_779040,Human_RBP_ID_9389667,Human_RBP_ID_18193806,Human_RBP_ID_24553481,Human_RBP_ID_26343836 Human_Splice_Rec_2101628,Human_Splice_Rec_2101706 RMVar_hsa_circ_127731,RMVar_hsa_circ_51024,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_26149,RMVar_hsa_circ_265778 83417 RMVar_ID_83417 Human_SNP_ID_686663741 m1A Human chr20 - 62319040 62319040 62319040 GCAGGCAGAGGTGCACTAGTACGGGCGGCCCCAGGCTCTGACGAACCCCTGCCCCACAGAGCTCA GCAGGCAGAGGTGCACTAGTACGGGCGGCCCCGGGCTCTGACGAACCCCTGCCCCACAGAGCTCA T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62318799..62319050 26863196 MeRIP-seq:(Medium) rs1209289875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5384048,Human_RBP_ID_8537786,Human_RBP_ID_9431700,Human_RBP_ID_22549464,Human_RBP_ID_22671103 RMVar_hsa_circ_127731,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_106659,RMVar_hsa_circ_265778,RMVar_hsa_circ_211220 83418 RMVar_ID_83418 Human_SNP_ID_686663790 m1A Human chr20 + 62319185 62319185 62319185 TAGAGCACCTGGCGAAAGGCCACAGCTGCCTCACCTGCCCGGCCCTCACCTCCTGCAGTGCCTCC TAGAGCACCTGGCGAAAGGCCACAGCTGCCTCGCCTGCCCGGCCCTCACCTCCTGCAGTGCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62319182..62319658 26863196 MeRIP-seq:(Medium) rs1173812631 Functional Loss SNV dbSNP153 33..33 33 - - - 83419 RMVar_ID_83419 Human_SNP_ID_686664036 m1A Human chr20 - 62319742 62319742 62319742 GCGAGCCAATTGCTGGCCGGCACCGAGGCCACACTGGGCCATGCGAAGACGCTGTTGGCGGCCAT GCGAGCCAATTGCTGGCCGGCACCGAGGCCACGCTGGGCCATGCGAAGACGCTGTTGGCGGCCAT T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62319147..62319794 26863196 MeRIP-seq:(Medium) rs995169744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9875 Human_Splice_Rec_2101625 RMVar_hsa_circ_127731,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_106659,RMVar_hsa_circ_265778,RMVar_hsa_circ_211220 83420 RMVar_ID_83420 Human_SNP_ID_686664045 m1A Human chr20 + 62319764 62319764 62319764 CATGGCCCAGTGTGGCCTCGGTGCCGGCCAGCAATTGGCTCGCCTGGTCTCGGGTCCCCACGGCC CATGGCCCAGTGTGGCCTCGGTGCCGGCCAGCCATTGGCTCGCCTGGTCTCGGGTCCCCACGGCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62319713..62322124 32194978 MeRIP-seq:(Medium) rs776411595 Functional Loss SNV dbSNP153 33..33 33 - - - 83421 RMVar_ID_83421 Human_SNP_ID_686665582 m1A Human chr20 - 62322376 62322376 62322376 GTGTGCTTGTGGACCGGCCGCCGAGGGCTCCGAGTGCCACCCCCAGAGCGGACAGTGCCACTGCC GTGTGCTTGTGGACCGGCCGCCGAGGGCTCCGCGTGCCACCCCCAGAGCGGACAGTGCCACTGCC T G LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62322327..62322572 26863196 MeRIP-seq:(Medium) rs758276838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62915,Human_RBP_ID_927061,Human_RBP_ID_3960405,Human_RBP_ID_19004542,Human_RBP_ID_21983372,Human_RBP_ID_22672203,Human_RBP_ID_23005243,Human_RBP_ID_26343213 Human_Splice_Rec_2101618 Human_miRNA_ID_2425814,Human_miRNA_ID_2435484 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_112429,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778 83422 RMVar_ID_83422 Human_SNP_ID_686665639 m1A Human chr20 - 62322463 62322463 62322463 GACAGTCTTGAGGGCTGGGCAGGGCAGTGACCAGCCTGTGCCACAGGAGGGACATTTTGGTTTCG GACAGTCTTGAGGGCTGGGCAGGGCAGTGACCGGCCTGTGCCACAGGAGGGACATTTTGGTTTCG T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62322460..62322547 26863196 MeRIP-seq:(Medium) rs1469717878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62916,Human_RBP_ID_2692780,Human_RBP_ID_5383117,Human_RBP_ID_18950886,Human_RBP_ID_19106974,Human_RBP_ID_22549465,Human_RBP_ID_22671108 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_112429,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778 83423 RMVar_ID_83423 Human_SNP_ID_686665841 m1A Human chr20 + 62322877 62322877 62322877 GCCTCCTGCTGTGTCTCCTCCAGGCCGCCCGGACCACCCGGCTACCCACTCGTGTCCCAGCCTGG GCCTCCTGCTGTGTCTCCTCCAGGCCGCCCGGGCCACCCGGCTACCCACTCGTGTCCCAGCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr20:62322726..62323050;chr20:62322676..62323025;chr20:62322701..62323025 26863196 MeRIP-seq:(Medium) rs1465931713 Functional Loss SNV dbSNP153 33..33 33 - - - 83424 RMVar_ID_83424 Human_SNP_ID_686666780 m1A Human chr20 + 62325148 62325148 62325148 GACGAGGGGCAGGCAGACAGGCAGCAGGGGACAGGCAGGCCCATGAGTTGGCCAGCAGCCTGTGA GACGAGGGGCAGGCAGACAGGCAGCAGGGGACGGGCAGGCCCATGAGTTGGCCAGCAGCCTGTGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62325101..62325150 26863196 MeRIP-seq:(Medium) rs1328727945 Functional Loss SNV dbSNP153 33..33 33 - - - 83425 RMVar_ID_83425 Human_SNP_ID_686666930 m1A Human chr20 + 62325476 62325476 62325476 GTGAGAAGAGGGCACGGATCTGCAGCTGCTCCAGGCTGGCCAGCACCATCATGAGCTCCTCGCGG GTGAGAAGAGGGCACGGATCTGCAGCTGCTCCGGGCTGGCCAGCACCATCATGAGCTCCTCGCGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62325451..62325475 26863196 MeRIP-seq:(Medium) rs757727996 Functional Loss SNV dbSNP153 33..33 33 - - - 83426 RMVar_ID_83426 Human_SNP_ID_686667257 m1A Human chr20 - 62326613 62326613 62326613 CTCATGGACCTCAGCTCATCTGGGAAGGCCGGAAGGGGTCCCAGTGCTGCTGTGCCCATTCTCCG CTCATGGACCTCAGCTCATCTGGGAAGGCCGGGAGGGGTCCCAGTGCTGCTGTGCCCATTCTCCG T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62326611..62326730 26863196 MeRIP-seq:(Medium) rs45596640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5383123,Human_RBP_ID_19109672,Human_RBP_ID_21983092 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778,RMVar_hsa_circ_344560,RMVar_hsa_circ_114824,RMVar_hsa_circ_211221,RMVar_hsa_circ_31782,RMVar_hsa_circ_211222 83427 RMVar_ID_83427 Human_SNP_ID_686667860 m1A Human chr20 + 62327968 62327968 62327968 GGGCGGCAGCGGGGGTAGCCATGGAAGCCCGGAGAGCAGGTATCACAGCGGCGCCCAGTCACGTT GGGCGGCAGCGGGGGTAGCCATGGAAGCCCGGGGAGCAGGTATCACAGCGGCGCCCAGTCACGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62327885..62328034 26863196 MeRIP-seq:(Medium) rs143224228 Functional Loss SNV dbSNP153 33..33 33 - - - 83428 RMVar_ID_83428 Human_SNP_ID_686668622 m1A Human chr20 + 62329841 62329841 62329841 CGGTCACAGTGAGCTCGCTGTGGGTCACGTCCAGCAGGGCCTGGCCCTCACACACCACCAGGGTG CGGTCACAGTGAGCTCGCTGTGGGTCACGTCCTGCAGGGCCTGGCCCTCACACACCACCAGGGTG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62329826..62329875 26863196 MeRIP-seq:(Medium) rs982861517 Functional Loss SNV dbSNP153 33..33 33 - - - 83429 RMVar_ID_83429 Human_SNP_ID_686668928 m1A Human chr20 + 62330565 62330565 62330565 TGGGGTGGGCTGGCTGGTAGCCGTGCAGCAGGAAGGCATAGCGGCCCAGCGTGGGCACATGGGTG TGGGGTGGGCTGGCTGGTAGCCGTGCAGCAGGCAGGCATAGCGGCCCAGCGTGGGCACATGGGTG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62330526..62331050 26863196 MeRIP-seq:(Medium) rs1246816343 Functional Loss SNV dbSNP153 33..33 33 - - - 83430 RMVar_ID_83430 Human_SNP_ID_686668948 m1A Human chr20 + 62330607 62330607 62330607 GGCCCAGCGTGGGCACATGGGTGGTGAAGACCACGGTGGCCTGCAGGGATAGGCCCTAGTGAGCA GGCCCAGCGTGGGCACATGGGTGGTGAAGACCGCGGTGGCCTGCAGGGATAGGCCCTAGTGAGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62330462..62330645 26863196 MeRIP-seq:(Medium) rs746914020 Functional Loss SNV dbSNP153 33..33 33 - - - 83431 RMVar_ID_83431 Human_SNP_ID_686669387 m1A Human chr20 - 62331380 62331380 62331380 AGGGCATCTTGGAAAGAGCAGGGCTCGGTCGGACGCCTGGGTTTGCAGTTTCCTGGGTCTGAGCT AGGGCATCTTGGAAAGAGCAGGGCTCGGTCGGTCGCCTGGGTTTGCAGTTTCCTGGGTCTGAGCT T A LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62331344..62331582 26863196 MeRIP-seq:(Medium) rs999764698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18495346,Human_RBP_ID_23005244 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778,RMVar_hsa_circ_78215,RMVar_hsa_circ_114824,RMVar_hsa_circ_211222,RMVar_hsa_circ_124058,RMVar_hsa_circ_211223,RMVar_hsa_circ_211225,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226 83432 RMVar_ID_83432 Human_SNP_ID_686669388 m1A Human chr20 - 62331380 62331380 62331380 AGGGCATCTTGGAAAGAGCAGGGCTCGGTCGGACGCCTGGGTTTGCAGTTTCCTGGGTCTGAGCT AGGGCATCTTGGAAAGAGCAGGGCTCGGTCGGGCGCCTGGGTTTGCAGTTTCCTGGGTCTGAGCT T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62331344..62331582 26863196 MeRIP-seq:(Medium) rs999764698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18495346,Human_RBP_ID_23005244 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778,RMVar_hsa_circ_78215,RMVar_hsa_circ_114824,RMVar_hsa_circ_211222,RMVar_hsa_circ_124058,RMVar_hsa_circ_211223,RMVar_hsa_circ_211225,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226 83433 RMVar_ID_83433 Human_SNP_ID_686669632 m1A Human chr20 - 62332155 62332155 62332155 GACGTACCCCCGAGCTGTTCCATGTGCTCAGGAAAGCACCTGCAGTCACAGCTCCCTGGCCCCAG GACGTACCCCCGAGCTGTTCCATGTGCTCAGGGAAGCACCTGCAGTCACAGCTCCCTGGCCCCAG T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62332121..62332251 26863196 MeRIP-seq:(Medium) rs1028553528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14162277,Human_RBP_ID_19110092,Human_RBP_ID_22478902 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778,RMVar_hsa_circ_78215,RMVar_hsa_circ_114824,RMVar_hsa_circ_211222,RMVar_hsa_circ_124058,RMVar_hsa_circ_211223,RMVar_hsa_circ_211225,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226 83434 RMVar_ID_83434 Human_SNP_ID_686670269 m1A Human chr20 - 62333525 62333523 62333525 CAGGGGCCAGAGTGAGGGCTGGGGGCCGGGTCAGGGGGTGGGGCCCACCACTCTCAGCACCACCT CAGGGGCCAGAGTGAGGGCTGGGGGCCGGGTC__GGGGTGGGGCCCACCACTCTCAGCACCACCT CCT C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62333344..62333685 26863196 MeRIP-seq:(Medium) rs758812952 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_62963,Human_RBP_ID_924185,Human_RBP_ID_2692794,Human_RBP_ID_5382765,Human_RBP_ID_19106995,Human_RBP_ID_22549480,Human_RBP_ID_22671127,Human_RBP_ID_27840577 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_265778,RMVar_hsa_circ_78215,RMVar_hsa_circ_114824,RMVar_hsa_circ_211222,RMVar_hsa_circ_124058,RMVar_hsa_circ_211223,RMVar_hsa_circ_211225,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226,RMVar_hsa_circ_127052,RMVar_hsa_circ_211229 83435 RMVar_ID_83435 Human_SNP_ID_686670539 m1A Human chr20 - 62334017 62334017 62334017 GCCCACCCAGCCCAGGATCGTGGCCAGGCTGAACCTGACCTCCCCTGACCTTTTCTGGCTCGTCT GCCCACCCAGCCCAGGATCGTGGCCAGGCTGAGCCTGACCTCCCCTGACCTTTTCTGGCTCGTCT T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62333890..62334040 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2101570 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_265778,RMVar_hsa_circ_78215,RMVar_hsa_circ_124058,RMVar_hsa_circ_211223,RMVar_hsa_circ_211225,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226,RMVar_hsa_circ_127052,RMVar_hsa_circ_211229,RMVar_hsa_circ_97168,RMVar_hsa_circ_211230 83436 RMVar_ID_83436 Human_SNP_ID_686671588 m1A Human chr20 - 62336311 62336310 62336311 ACCCGTGAGTGTGCCCTGGAGTATTGGGGTACAGGGGTTCCTTGGGGAACTGTGCCCACAAGTAT ACCCGTGAGTGTGCCCTGGAGTATTGGGGTAC_GGGGTTCCTTGGGGAACTGTGCCCACAAGTAT CT C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62336309..62336435 26863196 MeRIP-seq:(Medium) rs1484577991 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226,RMVar_hsa_circ_127052,RMVar_hsa_circ_211229 83437 RMVar_ID_83437 Human_SNP_ID_686671589 m1A Human chr20 - 62336311 62336311 62336311 ACCCGTGAGTGTGCCCTGGAGTATTGGGGTACAGGGGTTCCTTGGGGAACTGTGCCCACAAGTAT ACCCGTGAGTGTGCCCTGGAGTATTGGGGTACGGGGGTTCCTTGGGGAACTGTGCCCACAAGTAT T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62336309..62336435 26863196 MeRIP-seq:(Medium) rs191313800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_80387,RMVar_hsa_circ_211226,RMVar_hsa_circ_127052,RMVar_hsa_circ_211229 83438 RMVar_ID_83438 Human_SNP_ID_686674833 m1A Human chr20 - 62345776 62345776 62345776 CTTGAGGCCCCCAGGTCCCCGGCCTGCCCTGGAGCCATGGGGGCGGCTTCACAGAAAGTTCCTGG CTTGAGGCCCCCAGGTCCCCGGCCTGCCCTGGGGCCATGGGGGCGGCTTCACAGAAAGTTCCTGG T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62345774..62345913 26863196 MeRIP-seq:(Medium) rs1351807208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19109089 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_104880,RMVar_hsa_circ_211232 83439 RMVar_ID_83439 Human_SNP_ID_686675145 m1A Human chr20 + 62346524 62346524 62346524 CTGAGCCCACTCACGGCGGCAGACGTGGGGCGAGTCGAGAGGGTGGTTGGGAGAGCGGTAGAAGC CTGAGCCCACTCACGGCGGCAGACGTGGGGCGCGTCGAGAGGGTGGTTGGGAGAGCGGTAGAAGC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62346501..62346575 26863196 MeRIP-seq:(Medium) rs1275371427 Functional Loss SNV dbSNP153 33..33 33 - - - 83440 RMVar_ID_83440 Human_SNP_ID_686675351 m1A Human chr20 + 62346900 62346897 62346900 GCCAGGGTGTGGGCAGGACACACGTGTGTGGGAGGAGGCACTCACACTGGCACTCGTTGGCACTG GCCAGGGTGTGGGCAGGACACACGTGTGTG___GGAGGCACTCACACTGGCACTCGTTGGCACTG GGGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62346897..62346997 26863196 MeRIP-seq:(Medium) rs753836583 Functional Loss DEL dbSNP153 31..33 33 - - - 83441 RMVar_ID_83441 Human_SNP_ID_686677060 m1A Human chr20 - 62351774 62351774 62351774 TGCAGTATTATTACAGCATCAAGGATATCAGCATCGGAGGCCGCTGTGTCTGCCACGGCCACGCG TGCAGTATTATTACAGCATCAAGGATATCAGCGTCGGAGGCCGCTGTGTCTGCCACGGCCACGCG T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62351751..62351775 26863196 MeRIP-seq:(Medium) rs370349638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5595360,Human_RBP_ID_9391122,Human_RBP_ID_19004600,Human_RBP_ID_25624410 Human_Splice_Rec_2101536,Human_Splice_Rec_2101537,Human_Splice_Rec_2101734,Human_Splice_Rec_2101735,Human_Splice_Rec_2101748,Human_Splice_Rec_2101749 RMVar_hsa_circ_265237,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_84077,RMVar_hsa_circ_104880,RMVar_hsa_circ_211232,RMVar_hsa_circ_211237,RMVar_hsa_circ_211236,RMVar_hsa_circ_293798 83442 RMVar_ID_83442 Human_SNP_ID_686677381 m1A Human chr20 - 62352326 62352326 62352326 TCCAAGAGGGACTGTCTGGAGCGGTTCGGGCCACAGACGCTGGAGCGCATCACACGGGACGACGC TCCAAGAGGGACTGTCTGGAGCGGTTCGGGCCGCAGACGCTGGAGCGCATCACACGGGACGACGC T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62352179..62352381 26863196 MeRIP-seq:(Medium) rs747093531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63002,Human_RBP_ID_5595363 Human_Splice_Rec_2101532,Human_Splice_Rec_2101533,Human_Splice_Rec_2101730,Human_Splice_Rec_2101731 RMVar_hsa_circ_265237,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_84077,RMVar_hsa_circ_104880,RMVar_hsa_circ_211232,RMVar_hsa_circ_32274,RMVar_hsa_circ_211237,RMVar_hsa_circ_211236,RMVar_hsa_circ_293798,RMVar_hsa_circ_49508,RMVar_hsa_circ_92484,RMVar_hsa_circ_375621,RMVar_hsa_circ_211239,RMVar_hsa_circ_211240 83443 RMVar_ID_83443 Human_SNP_ID_686678012 m1A Human chr20 - 62354097 62354095 62354097 GGGCTGTCCCTGGGTGGAGGTCAGGCTGACACACGGGGAGAAAGTAGGCAGAGCCAAGGTGGGGC GGGCTGTCCCTGGGTGGAGGTCAGGCTGACAC__GGGGAGAAAGTAGGCAGAGCCAAGGTGGGGC CGT C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62354088..62354283 26863196 MeRIP-seq:(Medium) rs1309582638 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_265237,RMVar_hsa_circ_84077,RMVar_hsa_circ_104880,RMVar_hsa_circ_211232,RMVar_hsa_circ_211236,RMVar_hsa_circ_375621,RMVar_hsa_circ_211240 83444 RMVar_ID_83444 Human_SNP_ID_686680824 m1A Human chr20 + 62361984 62361984 62361984 GCCACCTCGGCACAGGTATCCCAGGAATGTCCACTTGCGCCAGCCTCCTCTGCATTCCTGCAGCC GCCACCTCGGCACAGGTATCCCAGGAATGTCCTCTTGCGCCAGCCTCCTCTGCATTCCTGCAGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62361975..62362175 26863196 MeRIP-seq:(Medium) rs1296046685 Functional Loss SNV dbSNP153 33..33 33 - - - 83445 RMVar_ID_83445 Human_SNP_ID_686682479 m1A Human chr20 + 62367175 62367175 62367175 CCCGCGCCGCGCCCAGCAGCGCCAGCCCGACCAGCAGCAGCGGCGCGGGGCCCCGGGGGCCGCGA CCCGCGCCGCGCCCAGCAGCGCCAGCCCGACCGGCAGCAGCGGCGCGGGGCCCCGGGGGCCGCGA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:62367126..62367325 26863196 MeRIP-seq:(Medium) rs956688861 Functional Loss SNV dbSNP153 33..33 33 - - - 83446 RMVar_ID_83446 Human_SNP_ID_686687625 m1A Human chr20 - 62382143 62382143 62382143 TCATCGTCACCACCATTGTCATCACCATCATCATCATCTTCACCATCATCTTCACTATCACCGTC TCATCGTCACCACCATTGTCATCACCATCATCTTCATCTTCACCATCATCTTCACTATCACCGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62382108..62382318 26863196 MeRIP-seq:(Medium) rs866588455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8537836,Human_RBP_ID_17396394,Human_RBP_ID_18534585,Human_RBP_ID_22260297 83447 RMVar_ID_83447 Human_SNP_ID_686689565 m1A Human chr20 + 62387135 62387135 62387135 CCTTTCTCTCTCGCGCGCGGTGTGGTGGCAGCAGGTGTGGCGCGCGGCGCGGGCTTCGGGCTCAG CCTTTCTCTCTCGCGCGCGGTGTGGTGGCAGCGGGTGTGGCGCGCGGCGCGGGCTTCGGGCTCAG A G RPS21 Ensembl:ENSG00000171858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEK293T,ALKBH3 KO chr20:62387101..62387150;chr20:62387076..62387150;chr20:62387101..62387175;chr20:62387076..62387175 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1002849670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244594,Human_RBP_ID_568171,Human_RBP_ID_779227,Human_RBP_ID_831547,Human_RBP_ID_4659519,Human_RBP_ID_17659094,Human_RBP_ID_22453178,Human_RBP_ID_23915228 Human_Splice_Rec_2101769,Human_Splice_Rec_2101779 RMVar_hsa_circ_211242,RMVar_hsa_circ_117978 83448 RMVar_ID_83448 Human_SNP_ID_686689680 m1A Human chr20 + 62387386 62387386 62387386 GGCGAGTTCGTGGACCTGTACGTGCCGCGGAAATGGTAAGCGCCCCCCACATGCCTCTCTTCCGT GGCGAGTTCGTGGACCTGTACGTGCCGCGGAAGTGGTAAGCGCCCCCCACATGCCTCTCTTCCGT A G RPS21 Ensembl:ENSG00000171858 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62387301..62387580 26863196 MeRIP-seq:(Medium) rs374417217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568174,Human_RBP_ID_779228,Human_RBP_ID_4659521,Human_RBP_ID_9118927,Human_RBP_ID_9331662,Human_RBP_ID_17659100,Human_RBP_ID_17976617,Human_RBP_ID_22452821,Human_RBP_ID_23212372,Human_RBP_ID_23915231 Human_Splice_Rec_2101770,Human_Splice_Rec_2101771,Human_Splice_Rec_2101780,Human_Splice_Rec_2101781,Human_Splice_Rec_2101787,Human_Splice_Rec_2101789,Human_Splice_Rec_2101795 RMVar_hsa_circ_101007,RMVar_hsa_circ_211242,RMVar_hsa_circ_117978,RMVar_hsa_circ_372104,RMVar_hsa_circ_211244,RMVar_hsa_circ_93426,RMVar_hsa_circ_211245,RMVar_hsa_circ_211243 83449 RMVar_ID_83449 Human_SNP_ID_686689698 m1A Human chr20 + 62387402 62387402 62387402 TGTACGTGCCGCGGAAATGGTAAGCGCCCCCCACATGCCTCTCTTCCGTCCTTACCTAACCACCA TGTACGTGCCGCGGAAATGGTAAGCGCCCCCCCCATGCCTCTCTTCCGTCCTTACCTAACCACCA A C RPS21 Ensembl:ENSG00000171858 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:62387396..62387602 26863196 MeRIP-seq:(Medium) rs1326178016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19109103 Human_Splice_Rec_2101770,Human_Splice_Rec_2101780 RMVar_hsa_circ_101007,RMVar_hsa_circ_211242,RMVar_hsa_circ_117978,RMVar_hsa_circ_372104,RMVar_hsa_circ_211244,RMVar_hsa_circ_211243 83450 RMVar_ID_83450 Human_SNP_ID_686689840 m1A Human chr20 - 62387604 62387604 62387604 CACCGATGATGCGATTGCTAGCGGAGCTGTGGAGAAAGGGCGCAGTGAGCAGAGGGGACTTGGGC CACCGATGATGCGATTGCTAGCGGAGCTGTGGGGAAAGGGCGCAGTGAGCAGAGGGGACTTGGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62387601..62387650 26863196 MeRIP-seq:(Medium) rs1332402222 Functional Loss SNV dbSNP153 33..33 33 - - - 83451 RMVar_ID_83451 Human_SNP_ID_686690292 m1A Human chr20 - 62388504 62388504 62388504 AATGAACCTGCACAGGTAGGTTTTCATTATTTATTTATGACAAATATTCCACATCTGTGATTCTC AATGAACCTGCACAGGTAGGTTTTCATTATTTGTTTATGACAAATATTCCACATCTGTGATTCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62388501..62388525 32194978 MeRIP-seq:(Medium) rs1404114209 Functional Loss SNV dbSNP153 33..33 33 - - - 83452 RMVar_ID_83452 Human_SNP_ID_686693611 m1A Human chr20 - 62398023 62398014 62398023 CCATCACCACCATCACCATCACTGTCACCACCACCACCACCGCCATAACCATCACCATCATCACC CCATCACCACCATCACCATCACTGTCACCACC_________GCCATAACCATCACCATCATCACC CGGTGGTGGT C CABLES2 Ensembl:ENSG00000149679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62397973..62398169 26863196 MeRIP-seq:(Medium) rs113048661 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_206727 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83453 RMVar_ID_83453 Human_SNP_ID_686693612 m1A Human chr20 - 62398023 62398014 62398023 CCATCACCACCATCACCATCACTGTCACCACCACCACCACCGCCATAACCATCACCATCATCACC CCATCACCACCATCACCATCACTGTCACCACC______ACCGCCATAACCATCACCATCATCACC CGGTGGTGGT CGGT CABLES2 Ensembl:ENSG00000149679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62397973..62398169 26863196 MeRIP-seq:(Medium) rs113048661 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_206727 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83454 RMVar_ID_83454 Human_SNP_ID_686693613 m1A Human chr20 - 62398023 62398014 62398023 CCATCACCACCATCACCATCACTGTCACCACCACCACCACCGCCATAACCATCACCATCATCACC CCATCACCACCATCACCATCACTGTCACCACC___ACCACCGCCATAACCATCACCATCATCACC CGGTGGTGGT CGGTGGT CABLES2 Ensembl:ENSG00000149679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62397973..62398169 26863196 MeRIP-seq:(Medium) rs113048661 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_206727 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83455 RMVar_ID_83455 Human_SNP_ID_686693631 m1A Human chr20 - 62398023 62398023 62398023 CCATCACCACCATCACCATCACTGTCACCACCACCACCACCGCCATAACCATCACCATCATCACC CCATCACCACCATCACCATCACTGTCACCACCTCCACCACCGCCATAACCATCACCATCATCACC T A CABLES2 Ensembl:ENSG00000149679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62397973..62398169 26863196 MeRIP-seq:(Medium) rs1228404829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206727 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83456 RMVar_ID_83456 Human_SNP_ID_686694126 m1A Human chr20 + 62398249 62398246 62398249 TGGTGGTGGTGGTGACGGTGGTGATGATGGTGATGGTGGTGGTGATGGTGATGGCGGTGGTGGTG TGGTGGTGGTGGTGACGGTGGTGATGATGG___TGGTGGTGGTGATGGTGATGGCGGTGGTGGTG GTGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62398242..62398399 26863196 MeRIP-seq:(Medium) rs1427969356 Functional Loss DEL dbSNP153 31..33 33 - - - 83457 RMVar_ID_83457 Human_SNP_ID_686694128 m1A Human chr20 + 62398249 62398249 62398249 TGGTGGTGGTGGTGACGGTGGTGATGATGGTGATGGTGGTGGTGATGGTGATGGCGGTGGTGGTG TGGTGGTGGTGGTGACGGTGGTGATGATGGTGGTGGTGGTGGTGATGGTGATGGCGGTGGTGGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62398242..62398399 26863196 MeRIP-seq:(Medium) rs1043213459 Functional Loss SNV dbSNP153 33..33 33 - - - 83458 RMVar_ID_83458 Human_SNP_ID_686696675 m1A Human chr20 - 62406954 62406954 62406954 CCCCGCGCCCCAGGGCCTGCTCAGCCCCACGCAGGTGCCCACCGGCCTCGGCCTGGATGGGCAGC CCCCGCGCCCCAGGGCCTGCTCAGCCCCACGCGGGTGCCCACCGGCCTCGGCCTGGATGGGCAGC T C CABLES2 Ensembl:ENSG00000149679 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62406891..62407078 26863196 MeRIP-seq:(Medium) rs770166252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5200530 Human_Splice_Rec_2101799 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83459 RMVar_ID_83459 Human_SNP_ID_686696676 m1A Human chr20 - 62406954 62406954 62406954 CCCCGCGCCCCAGGGCCTGCTCAGCCCCACGCAGGTGCCCACCGGCCTCGGCCTGGATGGGCAGC CCCCGCGCCCCAGGGCCTGCTCAGCCCCACGCCGGTGCCCACCGGCCTCGGCCTGGATGGGCAGC T G CABLES2 Ensembl:ENSG00000149679 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62406891..62407078 26863196 MeRIP-seq:(Medium) rs770166252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5200530 Human_Splice_Rec_2101799 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83460 RMVar_ID_83460 Human_SNP_ID_686696726 m1A Human chr20 - 62407090 62407090 62407090 TCAACAACATCTCCCTGGACGGGCGGCCCCCGAGCCTGGGCCCGGGCGGAGAGAAGCCCCCGCCG TCAACAACATCTCCCTGGACGGGCGGCCCCCGGGCCTGGGCCCGGGCGGAGAGAAGCCCCCGCCG T C CABLES2 Ensembl:ENSG00000149679 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62406925..62407235 26863196 MeRIP-seq:(Medium) rs1465921472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659987,Human_RBP_ID_22722652 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83461 RMVar_ID_83461 Human_SNP_ID_686696772 m1A Human chr20 - 62407201 62407201 62407201 GCCCCGCCGGGCCCCCGCCACCCGCCGCGCCGACCTCGGCCGCTCGGGCCCCGCCGCAGGCGCTG GCCCCGCCGGGCCCCCGCCACCCGCCGCGCCGCCCTCGGCCGCTCGGGCCCCGCCGCAGGCGCTG T G CABLES2 Ensembl:ENSG00000149679 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr20:62407152..62407282;chr20:62406985..62407285 26863196,26863410 MeRIP-seq:(Medium) rs981469111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659524,Human_RBP_ID_18422941,Human_RBP_ID_26788618 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83462 RMVar_ID_83462 Human_SNP_ID_686696782 m1A Human chr20 - 62407214 62407214 62407214 GGCCCGGCCCCCGGCCCCGCCGGGCCCCCGCCACCCGCCGCGCCGACCTCGGCCGCTCGGGCCCC GGCCCGGCCCCCGGCCCCGCCGGGCCCCCGCCCCCCGCCGCGCCGACCTCGGCCGCTCGGGCCCC T G CABLES2 Ensembl:ENSG00000149679 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:62406998..62407285 26863410 MeRIP-seq:(Medium) rs926875503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659524,Human_RBP_ID_18422941,Human_RBP_ID_26788618 RMVar_hsa_circ_91901,RMVar_hsa_circ_211250 83463 RMVar_ID_83463 Human_SNP_ID_686754080 m1A Human chr20 + 62594834 62594813 62594835 CCCTCATGCACGCCCTGCTGACCATCCCACTCACCCCTGCTGACCGTCCCGCTCACCCCTGCTGA CCCTCATGCACG______________________CCCTGCTGACCGTCCCGCTCACCCCTGCTGA GCCCTGCTGACCATCCCACTCAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62594826..62594895 26863196 MeRIP-seq:(Medium) rs1329290899 Functional Loss DEL dbSNP153 13..34 33 - - - 83464 RMVar_ID_83464 Human_SNP_ID_686754095 m1A Human chr20 + 62594834 62594834 62594834 CCCTCATGCACGCCCTGCTGACCATCCCACTCACCCCTGCTGACCGTCCCGCTCACCCCTGCTGA CCCTCATGCACGCCCTGCTGACCATCCCACTCTCCCCTGCTGACCGTCCCGCTCACCCCTGCTGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62594826..62594895 26863196 MeRIP-seq:(Medium) rs1039656947 Functional Loss SNV dbSNP153 33..33 33 - - - 83465 RMVar_ID_83465 Human_SNP_ID_686756343 m1A Human chr20 - 62603018 62603018 62603018 CTCAGATCCACATGGCAACACAAGCAGCTAAAACGCAGATAGAAACCCCAACCTGGGAAAAGGAG CTCAGATCCACATGGCAACACAAGCAGCTAAAGCGCAGATAGAAACCCCAACCTGGGAAAAGGAG T C BX640514.2 Ensembl:ENSG00000273812 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62602692..62603159 26863196 MeRIP-seq:(Medium) rs1290390605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2101919,Human_Splice_Rec_2101921,Human_Splice_Rec_2101923 83466 RMVar_ID_83466 Human_SNP_ID_686756345 m1A Human chr20 - 62603029 62603029 62603029 CAAGCCCCACTCTCAGATCCACATGGCAACACAAGCAGCTAAAACGCAGATAGAAACCCCAACCT CAAGCCCCACTCTCAGATCCACATGGCAACACCAGCAGCTAAAACGCAGATAGAAACCCCAACCT T G BX640514.2 Ensembl:ENSG00000273812 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62602861..62603152 26863196 MeRIP-seq:(Medium) rs1355336842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2101919,Human_Splice_Rec_2101921,Human_Splice_Rec_2101923 83467 RMVar_ID_83467 Human_SNP_ID_686756348 m1A Human chr20 - 62603041 62603041 62603041 TTGTCTGGAGGGCAAGCCCCACTCTCAGATCCACATGGCAACACAAGCAGCTAAAACGCAGATAG TTGTCTGGAGGGCAAGCCCCACTCTCAGATCCCCATGGCAACACAAGCAGCTAAAACGCAGATAG T G BX640514.2 Ensembl:ENSG00000273812 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62603029..62603115 26863196 MeRIP-seq:(Medium) rs1335714831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2101919,Human_Splice_Rec_2101921,Human_Splice_Rec_2101923 83468 RMVar_ID_83468 Human_SNP_ID_686761145 m1A Human chr20 - 62620922 62620922 62620922 GTGACGGCTTTTGCATGGGTCCTCCGGGCAGCAGGCAGGGCTTGCACAGGGGTATGGGGCTTGGG GTGACGGCTTTTGCATGGGTCCTCCGGGCAGCTGGCAGGGCTTGCACAGGGGTATGGGGCTTGGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62620829..62621052 26863196 MeRIP-seq:(Medium) rs1467560066 Functional Loss SNV dbSNP153 33..33 33 - - - 83469 RMVar_ID_83469 Human_SNP_ID_686766703 m1A Human chr20 + 62642545 62642542 62642546 GCGCTGCGCGGCGCGGCGGCCGGGCCCTCGAGACGGGGACGGTGAGTGCGCGGGGAGCGGGGAGC GCGCTGCGCGGCGCGGCGGCCGGGCCCTCG____GGGGACGGTGAGTGCGCGGGGAGCGGGGAGC GAGAC G SLCO4A1 Ensembl:ENSG00000101187 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62642494..62643161 26863196 MeRIP-seq:(Medium) rs1481660432 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4659525,Human_RBP_ID_18422942 Human_Splice_Rec_2101935,Human_Splice_Rec_2101957 83470 RMVar_ID_83470 Human_SNP_ID_686766707 m1A Human chr20 + 62642551 62642551 62642551 CGCGGCGCGGCGGCCGGGCCCTCGAGACGGGGACGGTGAGTGCGCGGGGAGCGGGGAGCTGGCGC CGCGGCGCGGCGGCCGGGCCCTCGAGACGGGGGCGGTGAGTGCGCGGGGAGCGGGGAGCTGGCGC A G SLCO4A1 Ensembl:ENSG00000101187 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:62642353..62643205;chr20:62642353..62643145 26863196 MeRIP-seq:(Medium) rs1157803228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659525,Human_RBP_ID_18422942 Human_Splice_Rec_2101935,Human_Splice_Rec_2101957 83471 RMVar_ID_83471 Human_SNP_ID_686766718 m1A Human chr20 + 62642575 62642575 62642575 AGACGGGGACGGTGAGTGCGCGGGGAGCGGGGAGCTGGCGCGGGTGCACAGGGCCCGACCTGCTG AGACGGGGACGGTGAGTGCGCGGGGAGCGGGGCGCTGGCGCGGGTGCACAGGGCCCGACCTGCTG A C SLCO4A1 Ensembl:ENSG00000101187 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62642569..62642738 26863196 MeRIP-seq:(Medium) rs1402751413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3655299,Human_RBP_ID_8204266,Human_RBP_ID_8729230,Human_RBP_ID_18422943,Human_RBP_ID_19107006,Human_RBP_ID_22417739,Human_RBP_ID_22743709,Human_RBP_ID_24553488,Human_RBP_ID_26788619 83472 RMVar_ID_83472 Human_SNP_ID_686766898 m1A Human chr20 + 62643058 62643058 62643058 CTGCTGCCGAGTCAAGGAGGAAACCTTCATGCACGGAAGTTTCTCGGGGGCGGCCGGGCTTTGTT CTGCTGCCGAGTCAAGGAGGAAACCTTCATGCCCGGAAGTTTCTCGGGGGCGGCCGGGCTTTGTT A C SLCO4A1 Ensembl:ENSG00000101187 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62643055..62643155 26863196 MeRIP-seq:(Medium) rs1339605226 Functional Loss SNV dbSNP153 33..33 33 - - - 83473 RMVar_ID_83473 Human_SNP_ID_686770795 m1A Human chr20 - 62656595 62656591 62656596 GGCTGCTTGCTGGTGTCCAGGGGGCTATGGGCAGCGGAGCGGAGGGAGCCGGGGCTCAGGGGTGT GGCTGCTTGCTGGTGTCCAGGGGGCTATGGG_____GAGCGGAGGGAGCCGGGGCTCAGGGGTGT CCGCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62656333..62656729 26863196 MeRIP-seq:(Medium) rs1569127900 Functional Loss DEL dbSNP153 32..36 33 - - - 83474 RMVar_ID_83474 Human_SNP_ID_686770883 m1A Human chr20 + 62656730 62656730 62656730 CAGAGCGTGGCGTGCGGCTGGTGGGCCTTCGCACCGCCGTGCCTGCAGGTCCTCAACACGCCCAA CAGAGCGTGGCGTGCGGCTGGTGGGCCTTCGCGCCGCCGTGCCTGCAGGTCCTCAACACGCCCAA A G SLCO4A1 Ensembl:ENSG00000101187 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62656685..62656757 26863196 MeRIP-seq:(Medium) rs758408429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18463506,Human_RBP_ID_22453186,Human_RBP_ID_27488021 RMVar_hsa_circ_5755,RMVar_hsa_circ_284567 83475 RMVar_ID_83475 Human_SNP_ID_686770970 m1A Human chr20 + 62656893 62656893 62656893 ACCTGCACAGCTACCAGAGCGGGCTCATCGCCAGCTCCTACGACATTGCCGCCTGCCTCTGCCTC ACCTGCACAGCTACCAGAGCGGGCTCATCGCCGGCTCCTACGACATTGCCGCCTGCCTCTGCCTC A G SLCO4A1 Ensembl:ENSG00000101187 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62656845..62656975 26863196 MeRIP-seq:(Medium) rs768271436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_724231 RMVar_hsa_circ_5755,RMVar_hsa_circ_284567 83476 RMVar_ID_83476 Human_SNP_ID_686771672 m1A Human chr20 + 62658751 62658751 62658751 ACCTGATTGGAGGTGCCCTGCTGAATATCTACACGGAAATGGGCCGACGGTGAGTGGCCGCGCAC ACCTGATTGGAGGTGCCCTGCTGAATATCTACGCGGAAATGGGCCGACGGTGAGTGGCCGCGCAC A G SLCO4A1 Ensembl:ENSG00000101187 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62658701..62658750 32194978 MeRIP-seq:(Medium) rs527382829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1932581,Human_RBP_ID_19006261,Human_RBP_ID_19109110 Human_Splice_Rec_2101938,Human_Splice_Rec_2101939,Human_Splice_Rec_2101960,Human_Splice_Rec_2101961,Human_Splice_Rec_2101976,Human_Splice_Rec_2101977 RMVar_hsa_circ_90950,RMVar_hsa_circ_5755,RMVar_hsa_circ_284567,RMVar_hsa_circ_211251 83477 RMVar_ID_83477 Human_SNP_ID_686773749 m1A Human chr20 - 62665046 62665046 62665046 GGCAGCTTCTGAGGCACTCAGGCTGAACTGGGACTCCAAGAACTTGGGGCTGAACGTGGACATGC GGCAGCTTCTGAGGCACTCAGGCTGAACTGGGCCTCCAAGAACTTGGGGCTGAACGTGGACATGC T G SLCO4A1-AS1 Ensembl:ENSG00000232803 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:62664998..62665098 32194978 MeRIP-seq:(Medium) rs772635184 Functional Loss SNV dbSNP153 33..33 33 - - - 83478 RMVar_ID_83478 Human_SNP_ID_686775874 m1A Human chr20 - 62670814 62670814 62670814 GGACAAAGTGGAATGCGAGGGTGTTTATAAGGAGACACCGTGTGCTCCCCCGCTACAATTAACAT GGACAAAGTGGAATGCGAGGGTGTTTATAAGGCGACACCGTGTGCTCCCCCGCTACAATTAACAT T G HSALNG0131555 RNACentral:URS0000EB7CF2 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62670776..62670875 32194978 MeRIP-seq:(Medium) rs1320323448 Functional Loss SNV dbSNP153 33..33 33 - - - 83479 RMVar_ID_83479 Human_SNP_ID_686799518 m1A Human chr20 - 62755298 62755298 62755298 AGGGAGGAAGGAAGGGAGGGAGAGGTAGAGGAATGAATGGAGGGAAGGAGGGAGAGAGGGATGGA AGGGAGGAAGGAAGGGAGGGAGAGGTAGAGGAGTGAATGGAGGGAAGGAGGGAGAGAGGGATGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62755250..62755351 26863196 MeRIP-seq:(Medium) rs867329508 Functional Loss SNV dbSNP153 33..33 33 - - - 83480 RMVar_ID_83480 Human_SNP_ID_686812063 m1A Human chr20 - 62796525 62796525 62796525 CGGCGCCCCCGCCGCCCACCTCGGCCTCTCCCATGGCCGCGGCCCGGCCGAGCAAGGAGCCCCCG CGGCGCCCCCGCCGCCCACCTCGGCCTCTCCCGTGGCCGCGGCCCGGCCGAGCAAGGAGCCCCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62796476..62796693 26863196 MeRIP-seq:(Medium) rs1216828562 Functional Loss SNV dbSNP153 33..33 33 - - - 83481 RMVar_ID_83481 Human_SNP_ID_686812093 m1A Human chr20 + 62796579 62796579 62796579 CGGGGGCGCCGCAGGCGACAAGGGCCCGGGGGAGGCGGCCACCAGCCCGGCGGAGGAGACAGTGG CGGGGGCGCCGCAGGCGACAAGGGCCCGGGGGGGGCGGCCACCAGCCCGGCGGAGGAGACAGTGG A G MRGBP Ensembl:ENSG00000101189 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62796451..62796650 26863196 MeRIP-seq:(Medium) rs1438489055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831523,Human_RBP_ID_4659533,Human_RBP_ID_8942853,Human_RBP_ID_9354045,Human_RBP_ID_18423228,Human_RBP_ID_26342548 Human_Splice_Rec_2102093 RMVar_hsa_circ_86323,RMVar_hsa_circ_211262 83482 RMVar_ID_83482 Human_SNP_ID_686812525 m1A Human chr20 + 62797745 62797745 62797745 GGTGAATTTGGTGACTTCTGTGGGAGTCAGACAAGTAGAGTTCCAGTCCTCGCAGAGCTTGGAGC GGTGAATTTGGTGACTTCTGTGGGAGTCAGACCAGTAGAGTTCCAGTCCTCGCAGAGCTTGGAGC A C MRGBP Ensembl:ENSG00000101189 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62797740..62797906 26863196 MeRIP-seq:(Medium) rs1448716738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281569 RMVar_hsa_circ_86323,RMVar_hsa_circ_27300,RMVar_hsa_circ_96834,RMVar_hsa_circ_211262,RMVar_hsa_circ_211263 83483 RMVar_ID_83483 Human_SNP_ID_686812813 m1A Human chr20 + 62798697 62798697 62798697 GAAGGTGAGGCTCGGGAAAGGTTGGGCTTGGGATTCAGAAAAGGCCAGACCCTGGCCAAGGGCAG GAAGGTGAGGCTCGGGAAAGGTTGGGCTTGGGGTTCAGAAAAGGCCAGACCCTGGCCAAGGGCAG A G MRGBP Ensembl:ENSG00000101189 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62798651..62798984 26863196 MeRIP-seq:(Medium) rs1448789383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9391128,Human_RBP_ID_19004609,Human_RBP_ID_19107014,Human_RBP_ID_21983115,Human_RBP_ID_27819972 RMVar_hsa_circ_86323,RMVar_hsa_circ_105407,RMVar_hsa_circ_96834,RMVar_hsa_circ_211262,RMVar_hsa_circ_211263,RMVar_hsa_circ_211264 83484 RMVar_ID_83484 Human_SNP_ID_686812822 m1A Human chr20 + 62798722 62798717 62798723 GCTTGGGATTCAGAAAAGGCCAGACCCTGGCCAAGGGCAGGGAGGTGAGGGTGAGGACCCCGGGC GCTTGGGATTCAGAAAAGGCCAGACCCT______GGGCAGGGAGGTGAGGGTGAGGACCCCGGGC TGGCCAA T MRGBP Ensembl:ENSG00000101189 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62798672..62798965 26863196 MeRIP-seq:(Medium) rs1568731735 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_924197,Human_RBP_ID_5385661,Human_RBP_ID_9389684,Human_RBP_ID_19004609,Human_RBP_ID_21983115,Human_RBP_ID_27819972 RMVar_hsa_circ_86323,RMVar_hsa_circ_105407,RMVar_hsa_circ_96834,RMVar_hsa_circ_211262,RMVar_hsa_circ_211263,RMVar_hsa_circ_211264 83485 RMVar_ID_83485 Human_SNP_ID_686814753 m1A Human chr20 + 62804894 62804894 62804894 GGACGACCCCGACTGCGACTCCACCTGGGAGGAGGACGAGGAGGATGCGGAGGACGCGGAGGACG GGACGACCCCGACTGCGACTCCACCTGGGAGGCGGACGAGGAGGATGCGGAGGACGCGGAGGACG A C OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:62804801..62805996;chr20:62804801..62805888 26863196 MeRIP-seq:(Medium) rs1437407922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779597,Human_RBP_ID_4665629,Human_RBP_ID_9389686,Human_RBP_ID_23004800 83486 RMVar_ID_83486 Human_SNP_ID_686814754 m1A Human chr20 + 62804894 62804894 62804894 GGACGACCCCGACTGCGACTCCACCTGGGAGGAGGACGAGGAGGATGCGGAGGACGCGGAGGACG GGACGACCCCGACTGCGACTCCACCTGGGAGGGGGACGAGGAGGATGCGGAGGACGCGGAGGACG A G OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:62804801..62805996;chr20:62804801..62805888 26863196 MeRIP-seq:(Medium) rs1437407922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779597,Human_RBP_ID_4665629,Human_RBP_ID_9389686,Human_RBP_ID_23004800 83487 RMVar_ID_83487 Human_SNP_ID_686814771 m1A Human chr20 - 62804932 62804924 62804933 GTCCCTCGCGCCGGCGGCCTCGCCGTCCTCGCAGTCCTCGTCCTCCGCGTCCTCCGCATCCTCCT GTCCCTCGCGCCGGCGGCCTCGCCGTCCTCG_________TCCTCCGCGTCCTCCGCATCCTCCT ACGAGGACTG A OGFR-AS1 Ensembl:ENSG00000229873 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62804883..62806284 32194978 MeRIP-seq:(Medium) rs931231817 Functional Loss DEL dbSNP153 32..40 33 - - - 83488 RMVar_ID_83488 Human_SNP_ID_686814776 m1A Human chr20 - 62804932 62804932 62804932 GTCCCTCGCGCCGGCGGCCTCGCCGTCCTCGCAGTCCTCGTCCTCCGCGTCCTCCGCATCCTCCT GTCCCTCGCGCCGGCGGCCTCGCCGTCCTCGCCGTCCTCGTCCTCCGCGTCCTCCGCATCCTCCT T G OGFR-AS1 Ensembl:ENSG00000229873 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62804883..62806284 32194978 MeRIP-seq:(Medium) rs773789963 Functional Loss SNV dbSNP153 33..33 33 - - - 83489 RMVar_ID_83489 Human_SNP_ID_686815213 m1A Human chr20 + 62806139 62806139 62806139 GTGGGCTGACTGTGTGGCCACATCCAGTCAGGACCCAGCCTCCAGAACTGACCCAGGGAGGCTCC GTGGGCTGACTGTGTGGCCACATCCAGTCAGGTCCCAGCCTCCAGAACTGACCCAGGGAGGCTCC A T OGFR Ensembl:ENSG00000060491 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62806135..62806291 26863196 MeRIP-seq:(Medium) rs1433907363 Functional Loss SNV dbSNP153 33..33 33 - - - 83490 RMVar_ID_83490 Human_SNP_ID_686815310 m1A Human chr20 - 62806477 62806470 62806477 CTCCACCTCCCAGGCAATCTCCACTCACTGCAACCTCCACCTCCCAGGTTTAAGCGATTCTCCTG CTCCACCTCCCAGGCAATCTCCACTCACTGCA_______CCTCCCAGGTTTAAGCGATTCTCCTG GTGGAGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62806471..62806740 26863196 MeRIP-seq:(Medium) rs542094487 Functional Loss DEL dbSNP153 33..39 33 - - - 83491 RMVar_ID_83491 Human_SNP_ID_686815312 m1A Human chr20 - 62806478 62806478 62806478 CCTCCACCTCCCAGGCAATCTCCACTCACTGCAACCTCCACCTCCCAGGTTTAAGCGATTCTCCT CCTCCACCTCCCAGGCAATCTCCACTCACTGCGACCTCCACCTCCCAGGTTTAAGCGATTCTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62806476..62806611 26863196 MeRIP-seq:(Medium) rs1297601010 Functional Loss SNV dbSNP153 33..33 33 - - - 83492 RMVar_ID_83492 Human_SNP_ID_686815489 m1A Human chr20 + 62807115 62807114 62807115 GAACACAGCCTGGTGACTTTAGTGTACAAAGCAGGGGGAGTCTCCAGGGGCACAGAACAGAGGCT GAACACAGCCTGGTGACTTTAGTGTACAAAGC_GGGGGAGTCTCCAGGGGCACAGAACAGAGGCT CA C OGFR Ensembl:ENSG00000060491 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62807113..62807249 26863196 MeRIP-seq:(Medium) rs1208854280 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2693020 83493 RMVar_ID_83493 Human_SNP_ID_686815588 m1A Human chr20 - 62807497 62807488 62807497 GAAAAGAGATGGGATTAGGACCCCCATGGGAGACCCCCAAGTGAGTCCCAACGTGGTGAGGGCTG GAAAAGAGATGGGATTAGGACCCCCATGGGAG_________TGAGTCCCAACGTGGTGAGGGCTG ACTTGGGGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62807494..62807626 26863196 MeRIP-seq:(Medium) rs1397160835 Functional Loss DEL dbSNP153 33..41 33 - - - 83494 RMVar_ID_83494 Human_SNP_ID_686815600 m1A Human chr20 - 62807504 62807504 62807504 CTGGGAAGAAAAGAGATGGGATTAGGACCCCCATGGGAGACCCCCAAGTGAGTCCCAACGTGGTG CTGGGAAGAAAAGAGATGGGATTAGGACCCCCCTGGGAGACCCCCAAGTGAGTCCCAACGTGGTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62807502..62807635 26863196 MeRIP-seq:(Medium) rs1448283484 Functional Loss SNV dbSNP153 33..33 33 - - - 83495 RMVar_ID_83495 Human_SNP_ID_686816298 m1A Human chr20 + 62809372 62809372 62809372 TTTGCCGCCAGCCAGCAACAAGGGTCCAGGTCACAGATGGCAGCAGGGCAAGGGCTGTGCATCGG TTTGCCGCCAGCCAGCAACAAGGGTCCAGGTCGCAGATGGCAGCAGGGCAAGGGCTGTGCATCGG A G OGFR Ensembl:ENSG00000060491 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62809368..62809457 26863196 MeRIP-seq:(Medium) rs1376031027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59386 83496 RMVar_ID_83496 Human_SNP_ID_686816300 m1A Human chr20 + 62809374 62809373 62809375 TGCCGCCAGCCAGCAACAAGGGTCCAGGTCACAGATGGCAGCAGGGCAAGGGCTGTGCATCGGAG TGCCGCCAGCCAGCAACAAGGGTCCAGGTCAC__ATGGCAGCAGGGCAAGGGCTGTGCATCGGAG CAG C OGFR Ensembl:ENSG00000060491 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62809371..62809471 26863196 MeRIP-seq:(Medium) rs1446728929 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_59386 83497 RMVar_ID_83497 Human_SNP_ID_686816660 m1A Human chr20 - 62810478 62810478 62810478 AGAGGAAACAGCCTGCAGGAGAAGAGATGCTCAGGCAAGGGATTAGGAGAGCCGCTTCCAGACCT AGAGGAAACAGCCTGCAGGAGAAGAGATGCTCGGGCAAGGGATTAGGAGAGCCGCTTCCAGACCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62810476..62810575 26863196 MeRIP-seq:(Medium) rs1448618673 Functional Loss SNV dbSNP153 33..33 33 - - - 83498 RMVar_ID_83498 Human_SNP_ID_686817527 m1A Human chr20 - 62812745 62812745 62812745 CCAGCTTCCTCTTCTTGCTCTCTTTGGGGCTTAAGGGCTCCGGCCTATCTTCCCCGTGGCCCCCT CCAGCTTCCTCTTCTTGCTCTCTTTGGGGCTTGAGGGCTCCGGCCTATCTTCCCCGTGGCCCCCT T C lnc-TCFL5-6 RNACentral:URS00008C27C3 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62811451..62813450 26863196 MeRIP-seq:(Medium) rs1412092717 Functional Loss SNV dbSNP153 33..33 33 - - - 83499 RMVar_ID_83499 Human_SNP_ID_686817529 m1A Human chr20 + 62812747 62812747 62812747 GGGGCCACGGGGAAGATAGGCCGGAGCCCTTAAGCCCCAAAGAGAGCAAGAAGAGGAAGCTGGAG GGGGCCACGGGGAAGATAGGCCGGAGCCCTTACGCCCCAAAGAGAGCAAGAAGAGGAAGCTGGAG A C OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:62812226..62813300;chr20:62811500..62813450 26863196 MeRIP-seq:(Medium) rs1482292388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831086,Human_RBP_ID_5147970,Human_RBP_ID_8234902,Human_RBP_ID_22081449,Human_RBP_ID_22722385 RMVar_hsa_circ_211266,RMVar_hsa_circ_88239 83500 RMVar_ID_83500 Human_SNP_ID_686817628 m1A Human chr20 + 62812973 62812973 62812973 CTGCCGCCAACCCCTGGGAGCCAGGGTGGCCGACAAGGTGAGGAAGCGGAGGAAGGTGGATGAGG CTGCCGCCAACCCCTGGGAGCCAGGGTGGCCGGCAAGGTGAGGAAGCGGAGGAAGGTGGATGAGG A G OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62812851..62813150 26863196 MeRIP-seq:(Medium) rs1012608913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4656321,Human_RBP_ID_5148533,Human_RBP_ID_9354140,Human_RBP_ID_19004613,Human_RBP_ID_20681561,Human_RBP_ID_22453625,Human_RBP_ID_26343234 Human_miRNA_ID_2999969 RMVar_hsa_circ_211266,RMVar_hsa_circ_88239 83501 RMVar_ID_83501 Human_SNP_ID_686817879 m1A Human chr20 - 62813391 62813331 62813391 CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTCATCCCTTGTAGGTCCTGCCGGGCTGGGGCCTGG CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTC_________________________________ CGAGCCAGCCGAGAGCCCATCGGAGACCCCAGGCCCCAGCCCGGCAGGACCTACAAGGGAT C lnc-TCFL5-6 RNACentral:URS00008C27C3 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62813351..62813450 26863196 MeRIP-seq:(Medium) rs1568741771 Functional Loss DEL dbSNP153 33..65 33 - - - 83502 RMVar_ID_83502 Human_SNP_ID_686817909 m1A Human chr20 - 62813391 62813391 62813391 CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTCATCCCTTGTAGGTCCTGCCGGGCTGGGGCCTGG CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTCTTCCCTTGTAGGTCCTGCCGGGCTGGGGCCTGG T A lnc-TCFL5-6 RNACentral:URS00008C27C3 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62813351..62813450 26863196 MeRIP-seq:(Medium) rs202064940 Functional Loss SNV dbSNP153 33..33 33 - - - 83503 RMVar_ID_83503 Human_SNP_ID_686817910 m1A Human chr20 - 62813391 62813391 62813391 CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTCATCCCTTGTAGGTCCTGCCGGGCTGGGGCCTGG CCTGGGGTCTCCGATGGGCTCTCGGCTGGCTCGTCCCTTGTAGGTCCTGCCGGGCTGGGGCCTGG T C lnc-TCFL5-6 RNACentral:URS00008C27C3 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62813351..62813450 26863196 MeRIP-seq:(Medium) rs202064940 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 83504 RMVar_ID_83504 Human_SNP_ID_686817943 m1A Human chr20 + 62813453 62813453 62813453 AGGCCCCCGCCCGGCAGGACCTGCAGGGGACGAGCCAGCCGAGAGCCCATCGGAGACCCCAGGCC AGGCCCCCGCCCGGCAGGACCTGCAGGGGACGCGCCAGCCGAGAGCCCATCGGAGACCCCAGGCC A C OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:62813353..62813468 26863410 MeRIP-seq:(Medium) rs562078272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211266,RMVar_hsa_circ_88239 83505 RMVar_ID_83505 Human_SNP_ID_686818032 m1A Human chr20 + 62813598 62813598 62813598 AGGGATGAGCCAGCCAAGGCGGGGGAGGCAGCAGAGTTGCAGGACGCAGAGGTGGAGTCTTCTGC AGGGATGAGCCAGCCAAGGCGGGGGAGGCAGCGGAGTTGCAGGACGCAGAGGTGGAGTCTTCTGC A G OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:62813526..62813975 26863196 MeRIP-seq:(Medium) rs777434114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4656330,Human_RBP_ID_22080169,Human_RBP_ID_27024002 RMVar_hsa_circ_211266,RMVar_hsa_circ_88239 83506 RMVar_ID_83506 Human_SNP_ID_686820683 m1A Human chr20 - 62821464 62821464 62821464 AAACATGGGGTCAGAGCCTGCCAGGCACAAGAAGGGCTGCGCCTCACCCCTCCCTAAGATGGCTC AAACATGGGGTCAGAGCCTGCCAGGCACAAGAGGGGCTGCGCCTCACCCCTCCCTAAGATGGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62821459..62821581 26863196 MeRIP-seq:(Medium) rs761358563 Functional Loss SNV dbSNP153 33..33 33 - - - 83507 RMVar_ID_83507 Human_SNP_ID_686820838 m1A Human chr20 - 62821812 62821812 62821812 GCACACTCTGAGGGGCTCTGGGACAGCCACTCACCGGGGGGCCGCGGAGGCCGATCCCACCTGGG GCACACTCTGAGGGGCTCTGGGACAGCCACTCGCCGGGGGGCCGCGGAGGCCGATCCCACCTGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62821706..62821854 26863196 MeRIP-seq:(Medium) rs776565960 Functional Loss SNV dbSNP153 33..33 33 - - - 83508 RMVar_ID_83508 Human_SNP_ID_686822066 m1A Human chr20 + 62825017 62825017 62825017 AGGCGAGCAGGGGGAAGTCGGCAAGGACGGCGAGAAGGTGAAGCTGCCGCACAGCAGCTGGGGAG AGGCGAGCAGGGGGAAGTCGGCAAGGACGGCGGGAAGGTGAAGCTGCCGCACAGCAGCTGGGGAG A G COL9A3 Ensembl:ENSG00000092758 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62824929..62825071 26863196 MeRIP-seq:(Medium) rs1056439745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18471191,Human_RBP_ID_19006287,Human_RBP_ID_22767500 Human_Splice_Rec_2102164,Human_Splice_Rec_2102186,Human_Splice_Rec_2102187,Human_Splice_Rec_2102246,Human_Splice_Rec_2102247,Human_Splice_Rec_2102272,Human_Splice_Rec_2102273,Human_Splice_Rec_2102278,Human_Splice_Rec_2102279 RMVar_hsa_circ_267262 83509 RMVar_ID_83509 Human_SNP_ID_686822211 m1A Human chr20 + 62825206 62825206 62825206 CGGGAGGGAGGGGCTGGGCTCCGGCGGTGGGGAGGGACCGTTTCATGGGTGCACCTGCACTGGCA CGGGAGGGAGGGGCTGGGCTCCGGCGGTGGGGCGGGACCGTTTCATGGGTGCACCTGCACTGGCA A C COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62825202..62825593 26863196 MeRIP-seq:(Medium) rs1367801069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3655364,Human_RBP_ID_8204308,Human_RBP_ID_9431737,Human_RBP_ID_18463129,Human_RBP_ID_18950943,Human_RBP_ID_19107038,Human_RBP_ID_21983124,Human_RBP_ID_22722725,Human_RBP_ID_26787998 RMVar_hsa_circ_267262 83510 RMVar_ID_83510 Human_SNP_ID_686822212 m1A Human chr20 + 62825206 62825206 62825206 CGGGAGGGAGGGGCTGGGCTCCGGCGGTGGGGAGGGACCGTTTCATGGGTGCACCTGCACTGGCA CGGGAGGGAGGGGCTGGGCTCCGGCGGTGGGGGGGGACCGTTTCATGGGTGCACCTGCACTGGCA A G COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62825202..62825593 26863196 MeRIP-seq:(Medium) rs1367801069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3655364,Human_RBP_ID_8204308,Human_RBP_ID_9431737,Human_RBP_ID_18463129,Human_RBP_ID_18950943,Human_RBP_ID_19107038,Human_RBP_ID_21983124,Human_RBP_ID_22722725,Human_RBP_ID_26787998 RMVar_hsa_circ_267262 83511 RMVar_ID_83511 Human_SNP_ID_686822886 m1A Human chr20 + 62826817 62826817 62826817 GGGCCGCCTGGGATCCCAGGAGCGCCTGGGAAAGCGGTACGTGTGTCAGTGGACGGTGGGCGCCA GGGCCGCCTGGGATCCCAGGAGCGCCTGGGAAGGCGGTACGTGTGTCAGTGGACGGTGGGCGCCA A G COL9A3 Ensembl:ENSG00000092758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62826724..62826878 26863196 MeRIP-seq:(Medium) rs752486948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354142,Human_RBP_ID_19004634,Human_RBP_ID_22453204,Human_RBP_ID_22767506,Human_RBP_ID_23005023 Human_Splice_Rec_2102192,Human_Splice_Rec_2102193,Human_Splice_Rec_2102252,Human_Splice_Rec_2102284,Human_Splice_Rec_2102285 RMVar_hsa_circ_267262 83512 RMVar_ID_83512 Human_SNP_ID_686823824 m1A Human chr20 - 62829476 62829476 62829476 GCCACATACCCGTTCTCCCTTCTCGCCTTTGGACCCCGCTCGTCCAGGGAGGCCCTGCCAGGAGA GCCACATACCCGTTCTCCCTTCTCGCCTTTGGTCCCCGCTCGTCCAGGGAGGCCCTGCCAGGAGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62827901..62831151 26863196 MeRIP-seq:(Medium) rs1337762367 Functional Loss SNV dbSNP153 33..33 33 - - - 83513 RMVar_ID_83513 Human_SNP_ID_686824217 m1A Human chr20 - 62830395 62830373 62830396 CCAACCTCACCCACCTGGAAGCCTCGGACACCAGGGGCTCCGGGAGGGCCTTGTGGGCCGAGGGC CCAACCTCACCCACCTGGAAGCCTCGGACAC_______________________GGGCCGAGGGC CACAAGGCCCTCCCGGAGCCCCTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62829806..62831151 32194978 MeRIP-seq:(Medium) rs606231470 Functional Loss DEL dbSNP153 32..54 33 - - - 83514 RMVar_ID_83514 Human_SNP_ID_686824231 m1A Human chr20 - 62830395 62830395 62830395 CCAACCTCACCCACCTGGAAGCCTCGGACACCAGGGGCTCCGGGAGGGCCTTGTGGGCCGAGGGC CCAACCTCACCCACCTGGAAGCCTCGGACACCTGGGGCTCCGGGAGGGCCTTGTGGGCCGAGGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62829806..62831151 32194978 MeRIP-seq:(Medium) rs1318592878 Functional Loss SNV dbSNP153 33..33 33 - - - 83515 RMVar_ID_83515 Human_SNP_ID_686824232 m1A Human chr20 - 62830395 62830395 62830395 CCAACCTCACCCACCTGGAAGCCTCGGACACCAGGGGCTCCGGGAGGGCCTTGTGGGCCGAGGGC CCAACCTCACCCACCTGGAAGCCTCGGACACCGGGGGCTCCGGGAGGGCCTTGTGGGCCGAGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62829806..62831151 32194978 MeRIP-seq:(Medium) rs1318592878 Functional Loss SNV dbSNP153 33..33 33 - - - 83516 RMVar_ID_83516 Human_SNP_ID_686824280 m1A Human chr20 + 62830493 62830493 62830493 GACGGGCCAGACCCGACAGGGTATGGGCACTGACGAGCCAGGACCTCCTTCCCCAGGGCCAGAAG GACGGGCCAGACCCGACAGGGTATGGGCACTGGCGAGCCAGGACCTCCTTCCCCAGGGCCAGAAG A G COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62830482..62830637 26863196 MeRIP-seq:(Medium) rs1221349900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2102211 83517 RMVar_ID_83517 Human_SNP_ID_686824530 m1A Human chr20 - 62830919 62830919 62830919 AGGAACACCACGTGGAAGGTCAGAGGGGCCAAAGGCGCCACAGTCGGGGCCCTGATGCCACTGCC AGGAACACCACGTGGAAGGTCAGAGGGGCCAACGGCGCCACAGTCGGGGCCCTGATGCCACTGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62830913..62831001 26863196 MeRIP-seq:(Medium) rs1398106774 Functional Loss SNV dbSNP153 33..33 33 - - - 83518 RMVar_ID_83518 Human_SNP_ID_686824898 m1A Human chr20 - 62832105 62832105 62832105 GGCTCTGGATTAGAGGAATGGCAGGAATCCCTAAAGTGAGCCTGCCCTGGGCCCAGGAATGGTAA GGCTCTGGATTAGAGGAATGGCAGGAATCCCTGAAGTGAGCCTGCCCTGGGCCCAGGAATGGTAA T C lnc-TCFL5-5 RNACentral:URS00008B25AA lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62832102..62832221 26863196 MeRIP-seq:(Medium) rs1204775431 Functional Loss SNV dbSNP153 33..33 33 - - - 83519 RMVar_ID_83519 Human_SNP_ID_686825166 m1A Human chr20 + 62832923 62832923 62832923 CCTGGGCTTTTGGCCTCGACCTTAAGATGAACATTACACCTACGGAGGCTTGAGAGCAGGGACTT CCTGGGCTTTTGGCCTCGACCTTAAGATGAACCTTACACCTACGGAGGCTTGAGAGCAGGGACTT A C COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62832918..62833007 26863196 MeRIP-seq:(Medium) rs184865274 Functional Loss SNV dbSNP153 33..33 33 - - - 83520 RMVar_ID_83520 Human_SNP_ID_686825167 m1A Human chr20 + 62832923 62832923 62832923 CCTGGGCTTTTGGCCTCGACCTTAAGATGAACATTACACCTACGGAGGCTTGAGAGCAGGGACTT CCTGGGCTTTTGGCCTCGACCTTAAGATGAACGTTACACCTACGGAGGCTTGAGAGCAGGGACTT A G COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62832918..62833007 26863196 MeRIP-seq:(Medium) rs184865274 Functional Loss SNV dbSNP153 33..33 33 - - - 83521 RMVar_ID_83521 Human_SNP_ID_686826234 m1A Human chr20 - 62835955 62835955 62835955 GATGGTGTCATCGGAACAGTCGCCGGGCACTCACCTCTCCTTTGGGTCCGACCAGGCCGCTGGGA GATGGTGTCATCGGAACAGTCGCCGGGCACTCGCCTCTCCTTTGGGTCCGACCAGGCCGCTGGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:62832850..62836006 26863196 MeRIP-seq:(Medium) rs1479738561 Functional Loss SNV dbSNP153 33..33 33 - - - 83522 RMVar_ID_83522 Human_SNP_ID_686826490 m1A Human chr20 + 62836430 62836430 62836430 GTTACTTTGCGGGGTGACGGTGGGAATGCCTCACCGAGGCTGCCGCCCCCATGCTGACGAATGTG GTTACTTTGCGGGGTGACGGTGGGAATGCCTCGCCGAGGCTGCCGCCCCCATGCTGACGAATGTG A G COL9A3 Ensembl:ENSG00000092758 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62836427..62836561 26863196 MeRIP-seq:(Medium) rs1349731756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22417766,Human_RBP_ID_22671661,Human_RBP_ID_22743726 83523 RMVar_ID_83523 Human_SNP_ID_686826738 m1A Human chr20 - 62837039 62837039 62837039 CAAGGGTGCAGGCGTTTACTCGAGAGAGGATCATCAGAAGTATTGTTACGTAAAGCATAAAATAT CAAGGGTGCAGGCGTTTACTCGAGAGAGGATCGTCAGAAGTATTGTTACGTAAAGCATAAAATAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62837036..62837116 26863196 MeRIP-seq:(Medium) rs755750138 Functional Loss SNV dbSNP153 33..33 33 - - - 83524 RMVar_ID_83524 Human_SNP_ID_686826891 m1A Human chr20 + 62837264 62837264 62837264 CCCACTGGGGAGCTGGGAGACCCCGGGCCCAGAGGTGAGTGTTTGACCCCATGACACGGTCACCC CCCACTGGGGAGCTGGGAGACCCCGGGCCCAGGGGTGAGTGTTTGACCCCATGACACGGTCACCC A G COL9A3 Ensembl:ENSG00000092758 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:62837163..62838732 26863410 MeRIP-seq:(Medium) rs1414767175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19006323,Human_RBP_ID_22767534 Human_Splice_Rec_2102223,Human_Splice_Rec_2102303,Human_Splice_Rec_2102337,Human_Splice_Rec_2102343,Human_Splice_Rec_2102347 83525 RMVar_ID_83525 Human_SNP_ID_686827441 m1A Human chr20 + 62838750 62838750 62838750 AGGAGCAGGGCTGGACGGGCCTGAAGGAGACCAGGGGCCCCAAGGTACGAGTCCACGGCCAGCAA AGGAGCAGGGCTGGACGGGCCTGAAGGAGACCCGGGGCCCCAAGGTACGAGTCCACGGCCAGCAA A C COL9A3 Ensembl:ENSG00000092758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62838648..62838799 26863196 MeRIP-seq:(Medium) rs1467744959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18167774,Human_RBP_ID_22767536 Human_Splice_Rec_2102224,Human_Splice_Rec_2102225,Human_Splice_Rec_2102304,Human_Splice_Rec_2102305,Human_Splice_Rec_2102338,Human_Splice_Rec_2102339,Human_Splice_Rec_2102344,Human_Splice_Rec_2102345,Human_Splice_Rec_2102348,Human_Splice_Rec_2102349 83526 RMVar_ID_83526 Human_SNP_ID_686828106 m1A Human chr20 - 62840554 62840553 62840554 CACCGTCCTGGCCGTCCTTGCTGGTGCCGGGCACGCCTTGGGGTCCTTGGGACAGAGCAGAAAGG CACCGTCCTGGCCGTCCTTGCTGGTGCCGGGC_CGCCTTGGGGTCCTTGGGACAGAGCAGAAAGG GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62840542..62840669 26863196 MeRIP-seq:(Medium) rs1568768774 Functional Loss DEL dbSNP153 33..33 33 - - - 83527 RMVar_ID_83527 Human_SNP_ID_686828197 m1A Human chr20 - 62840712 62840712 62840712 TCACGTTGAATTTTATGAGCTTCGAGAGCCTGATTTCTCCCCGACCCCTCCTAACACGGCTCCTT TCACGTTGAATTTTATGAGCTTCGAGAGCCTGGTTTCTCCCCGACCCCTCCTAACACGGCTCCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62840610..62840711 32194978 MeRIP-seq:(Medium) rs774339334 Functional Loss SNV dbSNP153 33..33 33 - - - 83528 RMVar_ID_83528 Human_SNP_ID_686828537 m1A Human chr20 - 62841586 62841585 62841586 TACACGGCTTTTTACTTATTTACCTTTTAAATATGCCCCTTTAGCAATTGGAACAAGTTAAATTG TACACGGCTTTTTACTTATTTACCTTTTAAAT_TGCCCCTTTAGCAATTGGAACAAGTTAAATTG AT A TCFL5 Ensembl:ENSG00000101190 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs202214865 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7019051,Human_RBP_ID_17019082,Human_RBP_ID_18324263 RMVar_hsa_circ_98382,RMVar_hsa_circ_269156,RMVar_hsa_circ_211267 83529 RMVar_ID_83529 Human_SNP_ID_686828538 m1A Human chr20 - 62841586 62841586 62841587 TACACGGCTTTTTACTTATTTACCTTTTAAATATGCCCCTTTAGCAATTGGAACAAGTTAAATTG TACACGGCTTTTTACTTATTTACCTTTTAAAATTGCCCCTTTAGCAATTGGAACAAGTTAAATTG TA AT TCFL5 Ensembl:ENSG00000101190 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs796466547 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_7019051,Human_RBP_ID_17019082,Human_RBP_ID_18324263 RMVar_hsa_circ_98382,RMVar_hsa_circ_269156,RMVar_hsa_circ_211267 83530 RMVar_ID_83530 Human_SNP_ID_686828539 m1A Human chr20 - 62841586 62841586 62841586 TACACGGCTTTTTACTTATTTACCTTTTAAATATGCCCCTTTAGCAATTGGAACAAGTTAAATTG TACACGGCTTTTTACTTATTTACCTTTTAAATTTGCCCCTTTAGCAATTGGAACAAGTTAAATTG T A TCFL5 Ensembl:ENSG00000101190 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12625609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7019051,Human_RBP_ID_17019082,Human_RBP_ID_18324263 GWAS_ID_10084,GWAS_ID_10085,GWAS_ID_10086,GWAS_ID_10087,GWAS_ID_10088 RMVar_hsa_circ_98382,RMVar_hsa_circ_269156,RMVar_hsa_circ_211267 83531 RMVar_ID_83531 Human_SNP_ID_686828540 m1A Human chr20 - 62841586 62841586 62841586 TACACGGCTTTTTACTTATTTACCTTTTAAATATGCCCCTTTAGCAATTGGAACAAGTTAAATTG TACACGGCTTTTTACTTATTTACCTTTTAAATCTGCCCCTTTAGCAATTGGAACAAGTTAAATTG T G TCFL5 Ensembl:ENSG00000101190 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12625609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7019051,Human_RBP_ID_17019082,Human_RBP_ID_18324263 GWAS_ID_10084,GWAS_ID_10085,GWAS_ID_10086,GWAS_ID_10087,GWAS_ID_10088 RMVar_hsa_circ_98382,RMVar_hsa_circ_269156,RMVar_hsa_circ_211267 83532 RMVar_ID_83532 Human_SNP_ID_686828653 m1A Human chr20 + 62841968 62841968 62841968 AATGGCTGTTCACCCCCCGAGGATTCCTGTTCAGTCCGATCACTTGATCTCCATCGAGGGGCTGC AATGGCTGTTCACCCCCCGAGGATTCCTGTTCGGTCCGATCACTTGATCTCCATCGAGGGGCTGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:62841918..62842069 26863196 MeRIP-seq:(Medium) rs753447877 Functional Loss SNV dbSNP153 33..33 33 - - - 83533 RMVar_ID_83533 Human_SNP_ID_686831364 m1A Human chr20 - 62850969 62850967 62850969 AAGATAGAGGCATGTCTGGCATGGAGGGAGGCAGGGGACGAGTAAACGTGAAGACAGTGGGAGCA AAGATAGAGGCATGTCTGGCATGGAGGGAGGC__GGGACGAGTAAACGTGAAGACAGTGGGAGCA CCT C TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:62850821..62850970 26863196 MeRIP-seq:(Medium) rs1265769101 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_98382,RMVar_hsa_circ_211267 83534 RMVar_ID_83534 Human_SNP_ID_686831584 m1A Human chr20 - 62851801 62851801 62851801 CATCTCAAAAGAAGGGCTCCTGTGTCTACGTCATGGTGGGGCTAGAGAGAGGTCCCCGCAGCTGG CATCTCAAAAGAAGGGCTCCTGTGTCTACGTCCTGGTGGGGCTAGAGAGAGGTCCCCGCAGCTGG T G TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62851750..62851868 26863196 MeRIP-seq:(Medium) rs1016303409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568326,Human_RBP_ID_4665654,Human_RBP_ID_8537973,Human_RBP_ID_22507027 Human_miRNA_ID_1968920 RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_211268 83535 RMVar_ID_83535 Human_SNP_ID_686831878 m1A Human chr20 + 62852767 62852767 62852767 AGCATAGTCACCTGGTCCGCAGAAGTATATTCACCCATTCCACAGAAGCACGGTCACCCGGTCCG AGCATAGTCACCTGGTCCGCAGAAGTATATTCCCCCATTCCACAGAAGCACGGTCACCCGGTCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62852719..62852824 26863196 MeRIP-seq:(Medium) rs1025649665 Functional Loss SNV dbSNP153 33..33 33 - - - 83536 RMVar_ID_83536 Human_SNP_ID_686831988 m1A Human chr20 - 62853015 62853015 62853015 CGGGTGACTATGCTTCTGTGGACCGGGTGACTATACTTCTGCGGACTGGGTGAATGTACTTCAGC CGGGTGACTATGCTTCTGTGGACCGGGTGACTGTACTTCTGCGGACTGGGTGAATGTACTTCAGC T C TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62852997..62853123 26863196 MeRIP-seq:(Medium) rs560952484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568340,Human_RBP_ID_5652620,Human_RBP_ID_8113605,Human_RBP_ID_8537977,Human_RBP_ID_8856757,Human_RBP_ID_18324275,Human_RBP_ID_18950952,Human_RBP_ID_20681562,Human_RBP_ID_23915345 RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_211269,RMVar_hsa_circ_211268,RMVar_hsa_circ_211270 83537 RMVar_ID_83537 Human_SNP_ID_686831989 m1A Human chr20 - 62853015 62853015 62853015 CGGGTGACTATGCTTCTGTGGACCGGGTGACTATACTTCTGCGGACTGGGTGAATGTACTTCAGC CGGGTGACTATGCTTCTGTGGACCGGGTGACTCTACTTCTGCGGACTGGGTGAATGTACTTCAGC T G TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62852997..62853123 26863196 MeRIP-seq:(Medium) rs560952484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568340,Human_RBP_ID_5652620,Human_RBP_ID_8113605,Human_RBP_ID_8537977,Human_RBP_ID_8856757,Human_RBP_ID_18324275,Human_RBP_ID_18950952,Human_RBP_ID_20681562,Human_RBP_ID_23915345 RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_211269,RMVar_hsa_circ_211268,RMVar_hsa_circ_211270 83538 RMVar_ID_83538 Human_SNP_ID_686834940 m1A Human chr20 - 62861404 62861393 62861405 TCGGCGCTGCTGGCGGCGGCGGGCCCGGGCGCAGGCGCGGGCGGCTTCGCGGCGGGCGGTCAGGG TCGGCGCTGCTGGCGGCGGCGGGCCCGGGCG____________GCTTCGCGGCGGGCGGTCAGGG CCGCCCGCGCCTG C TCFL5 Ensembl:ENSG00000101190 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:62861314..62861779 26863410 MeRIP-seq:(Medium) rs750257529 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_244238,Human_RBP_ID_23258361 RMVar_hsa_circ_121977,RMVar_hsa_circ_211268 83539 RMVar_ID_83539 Human_SNP_ID_686835055 m1A Human chr20 - 62861648 62861648 62861648 CCGCGCCGCCATGTCGGGCCCCGGACCGCGGGAGCCGCCGCCGGAGGCAGGCGCGGCAGGCGGCG CCGCGCCGCCATGTCGGGCCCCGGACCGCGGGTGCCGCCGCCGGAGGCAGGCGCGGCAGGCGGCG T A TCFL5 Ensembl:ENSG00000101190 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62861601..62861675 26863196 MeRIP-seq:(Medium) rs1232352362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5472306,Human_RBP_ID_26787815 RMVar_hsa_circ_121977,RMVar_hsa_circ_211268 83540 RMVar_ID_83540 Human_SNP_ID_686840625 m1A Human chr20 - 62879447 62879447 62879447 AGAGCGCGAGGCCGACCGGGGCAAGGAGTGGGACCGCAGCCGGGAGCGGAGCAGGAACCGAGAGC AGAGCGCGAGGCCGACCGGGGCAAGGAGTGGGGCCGCAGCCGGGAGCGGAGCAGGAACCGAGAGC T C DIDO1 Ensembl:ENSG00000101191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:62879301..62879750;chr20:62879263..62879876 26863196 MeRIP-seq:(Medium) rs1349957428 Functional Loss SNV dbSNP153 33..33 33 - - - 83541 RMVar_ID_83541 Human_SNP_ID_686840724 m1A Human chr20 - 62879639 62879639 62879639 CAAAGAGAAGCCGCTGGAGGAGCCCGACGCCCAGGGCCGGGCGTCCGAGGACAGGAGGAGAGAGC CAAAGAGAAGCCGCTGGAGGAGCCCGACGCCCGGGGCCGGGCGTCCGAGGACAGGAGGAGAGAGC T C DIDO1 Ensembl:ENSG00000101191 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:62879546..62879671 26863196 MeRIP-seq:(Medium) rs773333280 Functional Loss SNV dbSNP153 33..33 33 - - - 83542 RMVar_ID_83542 Human_SNP_ID_686841932 m1A Human chr20 - 62882085 62882067 62882085 AACCTGCAGCCCCCAGCCCAGCCACAGCAGCCACAACAGCAGCGGCAGCCTCCACGGCAGCTTCC AACCTGCAGCCCCCAGCCCAGCCACAGCAGCC__________________TCCACGGCAGCTTCC AGGCTGCCGCTGCTGTTGT A DIDO1 Ensembl:ENSG00000101191 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62882036..62882253 26863196 MeRIP-seq:(Medium) rs1231473624 Functional Loss DEL dbSNP153 33..50 33 - - - 83543 RMVar_ID_83543 Human_SNP_ID_686841934 m1A Human chr20 - 62882085 62882074 62882086 AACCTGCAGCCCCCAGCCCAGCCACAGCAGCCACAACAGCAGCGGCAGCCTCCACGGCAGCTTCC AACCTGCAGCCCCCAGCCCAGCCACAGCAGC____________GGCAGCCTCCACGGCAGCTTCC CGCTGCTGTTGTG C DIDO1 Ensembl:ENSG00000101191 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62882036..62882253 26863196 MeRIP-seq:(Medium) rs374696200 Functional Loss DEL dbSNP153 32..43 33 - - - 83544 RMVar_ID_83544 Human_SNP_ID_686851209 m1A Human chr20 + 62910978 62910978 62910978 GATCGTTCTCGGGCTCCTGCTTACTGGGCAGGACGCCCTCCACAGTGTCACTGGCCTCGGAGCCC GATCGTTCTCGGGCTCCTGCTTACTGGGCAGGTCGCCCTCCACAGTGTCACTGGCCTCGGAGCCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62909988..62911141 32194978 MeRIP-seq:(Medium) rs754098928 Functional Loss SNV dbSNP153 33..33 33 - - - 83545 RMVar_ID_83545 Human_SNP_ID_686855894 m1A Human chr20 - 62926020 62926020 62926020 GTAGCTGGCTTGTAAGCGCAGCTGGTTTCCCTAGGCATTCTCGGGGACCTCGGCGCTTCCTCCCG GTAGCTGGCTTGTAAGCGCAGCTGGTTTCCCTGGGCATTCTCGGGGACCTCGGCGCTTCCTCCCG T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62926015..62926461 26863196 MeRIP-seq:(Medium) rs1252477871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5384175 RMVar_hsa_circ_118515,RMVar_hsa_circ_211281 83546 RMVar_ID_83546 Human_SNP_ID_686855895 m1A Human chr20 - 62926020 62926020 62926020 GTAGCTGGCTTGTAAGCGCAGCTGGTTTCCCTAGGCATTCTCGGGGACCTCGGCGCTTCCTCCCG GTAGCTGGCTTGTAAGCGCAGCTGGTTTCCCTCGGCATTCTCGGGGACCTCGGCGCTTCCTCCCG T G DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62926015..62926461 26863196 MeRIP-seq:(Medium) rs1252477871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5384175 RMVar_hsa_circ_118515,RMVar_hsa_circ_211281 83547 RMVar_ID_83547 Human_SNP_ID_686859509 m1A Human chr20 - 62937841 62937841 62937841 AGATGGCTGCTGCGGAGGCGTTGGAGCGCGGAAATCTGGAACCGGGATGGCGACGTCTACACTGA AGATGGCTGCTGCGGAGGCGTTGGAGCGCGGAGATCTGGAACCGGGATGGCGACGTCTACACTGA T C DIDO1 Ensembl:ENSG00000101191 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:62937675..62937875 26863196 MeRIP-seq:(Medium) rs943806759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244763,Human_RBP_ID_926257,Human_RBP_ID_3653200,Human_RBP_ID_4656701,Human_RBP_ID_9389710,Human_RBP_ID_14164825,Human_RBP_ID_18412877,Human_RBP_ID_18776831,Human_RBP_ID_19006336,Human_RBP_ID_23005034,Human_RBP_ID_26342555 Human_Splice_Rec_2102371,Human_Splice_Rec_2102455 83548 RMVar_ID_83548 Human_SNP_ID_686859650 m1A Human chr20 - 62938151 62938149 62938152 AGAGGTGGCGGCCGCCGGGGCGCCCGAGTAGAAGGAGGCAGAGGTGGGGGCCGCGGCGGAGGCGG AGAGGTGGCGGCCGCCGGGGCGCCCGAGTAG___GAGGCAGAGGTGGGGGCCGCGGCGGAGGCGG CCTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62938101..62938298 26863196 MeRIP-seq:(Medium) rs1299978346 Functional Loss DEL dbSNP153 32..34 33 - - - 83549 RMVar_ID_83549 Human_SNP_ID_686862087 m1A Human chr20 + 62946036 62946033 62946036 CTGCGTGCATTGCCTGCGAGTCGGGACAGTTGATGGGCACATGGCCTTGTAGCTCTGGGCACAGA CTGCGTGCATTGCCTGCGAGTCGGGACAGT___TGGGCACATGGCCTTGTAGCTCTGGGCACAGA TTGA T GID8 Ensembl:ENSG00000101193 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62945741..62946040 32194978 MeRIP-seq:(Medium) rs1568904520 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8856998,Human_RBP_ID_14165120 Human_miRNA_ID_2658979 RMVar_hsa_circ_82141,RMVar_hsa_circ_117884,RMVar_hsa_circ_211284,RMVar_hsa_circ_211286,RMVar_hsa_circ_211287,RMVar_hsa_circ_80037 83550 RMVar_ID_83550 Human_SNP_ID_686862088 m1A Human chr20 + 62946036 62946036 62946036 CTGCGTGCATTGCCTGCGAGTCGGGACAGTTGATGGGCACATGGCCTTGTAGCTCTGGGCACAGA CTGCGTGCATTGCCTGCGAGTCGGGACAGTTGGTGGGCACATGGCCTTGTAGCTCTGGGCACAGA A G GID8 Ensembl:ENSG00000101193 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62945741..62946040 32194978 MeRIP-seq:(Medium) rs1171240135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8856998,Human_RBP_ID_14165120 Human_miRNA_ID_2658979 RMVar_hsa_circ_82141,RMVar_hsa_circ_117884,RMVar_hsa_circ_211284,RMVar_hsa_circ_211286,RMVar_hsa_circ_211287,RMVar_hsa_circ_80037 83551 RMVar_ID_83551 Human_SNP_ID_686862445 m1A Human chr20 - 62947168 62947168 62947168 GCTGGATGCTGGCACTGGCTTATCATGAAGGGAAGGAGAGCAGTAACGCTGGAGACTTCCCAGTC GCTGGATGCTGGCACTGGCTTATCATGAAGGGGAGGAGAGCAGTAACGCTGGAGACTTCCCAGTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62947029..62947200 26863196 MeRIP-seq:(Medium) rs953313705 Functional Loss SNV dbSNP153 33..33 33 - - - 83552 RMVar_ID_83552 Human_SNP_ID_686862470 m1A Human chr20 - 62947256 62947256 62947256 TCACAAGAAAAGCAAGTGCAGCCCCTCACACGAAAGGAAGGCAGGCAGTAACATCGGAGACTTCC TCACAAGAAAAGCAAGTGCAGCCCCTCACACGCAAGGAAGGCAGGCAGTAACATCGGAGACTTCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:62947079..62947294 26863196 MeRIP-seq:(Medium) rs886315793 Functional Loss SNV dbSNP153 33..33 33 - - - 83553 RMVar_ID_83553 Human_SNP_ID_686922747 m1A Human chr20 - 63154823 63154823 63154823 AGGGGGAGGAGGGTGGGAAAGGGGGGAGGAGGAGGAAGGGAGAGGGAGGAGGAAAGAGGAGAGGG AGGGGGAGGAGGGTGGGAAAGGGGGGAGGAGGGGGAAGGGAGAGGGAGGAGGAAAGAGGAGAGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:63154801..63154850 26863196 MeRIP-seq:(Medium) rs1208981044 Functional Loss SNV dbSNP153 33..33 33 - - - 83554 RMVar_ID_83554 Human_SNP_ID_686934549 m1A Human chr20 - 63195930 63195921 63195930 TTTAAATTTTACACCTTTTCTTAAGAATTCTAATGCCGTCTTAAGTTTTTATACCAATAATGCTG TTTAAATTTTACACCTTTTCTTAAGAATTCTA_________TAAGTTTTTATACCAATAATGCTG AAGACGGCAT A YTHDF1 Ensembl:ENSG00000149658 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:63195894..63196100 26863196 MeRIP-seq:(Medium) rs1385211380 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_7026366,Human_RBP_ID_14165281,Human_RBP_ID_17283717,Human_RBP_ID_17396453,Human_RBP_ID_17512673,Human_RBP_ID_17975642,Human_RBP_ID_22422996 Human_miRNA_ID_855173,Human_miRNA_ID_2198313,Human_miRNA_ID_2198314,Human_miRNA_ID_2198544,Human_miRNA_ID_2198545 RMVar_hsa_circ_211295,RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_379001 83555 RMVar_ID_83555 Human_SNP_ID_686940165 m1A Human chr20 - 63215533 63215533 63215533 CCCGGGACGGCCGGCGCGGGCTGGAGTGGAGGAGGACGGGGAAGGAACGGTCCAGGAAGCTGCGT CCCGGGACGGCCGGCGCGGGCTGGAGTGGAGGGGGACGGGGAAGGAACGGTCCAGGAAGCTGCGT T C YTHDF1 Ensembl:ENSG00000149658 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63215524..63215697 26863196 MeRIP-seq:(Medium) rs775904179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924212,Human_RBP_ID_5323372,Human_RBP_ID_5382789,Human_RBP_ID_9347937,Human_RBP_ID_19107072,Human_RBP_ID_22671152,Human_RBP_ID_26787738 Human_Splice_Rec_2102664,Human_Splice_Rec_2102672 RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_112497,RMVar_hsa_circ_211298 83556 RMVar_ID_83556 Human_SNP_ID_686946515 m1A Human chr20 - 63235702 63235702 63235702 GCTGTGGGGGAGGGGTTGGGGAGCTGGAGATGATGGCTCCAAGGTCAGGCGCCCAGGGCAGCCTC GCTGTGGGGGAGGGGTTGGGGAGCTGGAGATGCTGGCTCCAAGGTCAGGCGCCCAGGGCAGCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63235667..63235795 26863196 MeRIP-seq:(Medium) rs1315356389 Functional Loss SNV dbSNP153 33..33 33 - - - 83557 RMVar_ID_83557 Human_SNP_ID_686958393 m1A Human chr20 + 63272858 63272858 63272858 GGCTGGTGGGCGACCGGGCGCATCCTCATTGCAGTGCGGCGGCCCTACCTCGGCCCTGGCCTGAC GGCTGGTGGGCGACCGGGCGCATCCTCATTGCGGTGCGGCGGCCCTACCTCGGCCCTGGCCTGAC A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63272801..63272962 26863196 MeRIP-seq:(Medium) rs1368539130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4657022,Human_RBP_ID_27024307 Human_Splice_Rec_2102777,Human_Splice_Rec_2102801,Human_Splice_Rec_2102823,Human_Splice_Rec_2102831,Human_Splice_Rec_2102855,Human_Splice_Rec_2102861,Human_Splice_Rec_2102883,Human_Splice_Rec_2102891,Human_Splice_Rec_2102915,Human_Splice_Rec_2102937,Human_Splice_Rec_2102947,Human_Splice_Rec_2102963,Human_Splice_Rec_2102989,Human_Splice_Rec_2103011 RMVar_hsa_circ_94309,RMVar_hsa_circ_211300 83558 RMVar_ID_83558 Human_SNP_ID_686958419 m1A Human chr20 + 63272919 63272919 63272919 TGACCCCGGCGGCCCTGCCCGCCCCTCCCTCCAGGTAAGCGCGCGGCTCGGCGGCGCGGGCTCGG TGACCCCGGCGGCCCTGCCCGCCCCTCCCTCCCGGTAAGCGCGCGGCTCGGCGGCGCGGGCTCGG A C ARFGAP1 Ensembl:ENSG00000101199 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63272868..63272975 26863196 MeRIP-seq:(Medium) rs1251751396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659998,Human_RBP_ID_19109179 Human_Splice_Rec_2102777,Human_Splice_Rec_2102801,Human_Splice_Rec_2102823,Human_Splice_Rec_2102831,Human_Splice_Rec_2102855,Human_Splice_Rec_2102861,Human_Splice_Rec_2102883,Human_Splice_Rec_2102891,Human_Splice_Rec_2102915,Human_Splice_Rec_2102937,Human_Splice_Rec_2102947,Human_Splice_Rec_2102963,Human_Splice_Rec_2102989,Human_Splice_Rec_2103011 RMVar_hsa_circ_94309,RMVar_hsa_circ_211300 83559 RMVar_ID_83559 Human_SNP_ID_686959337 m1A Human chr20 + 63275630 63275630 63275630 CAGGAAGGTTCTTAAAGAAGTCAGGGTGCAGGATGAGAACAACGTAAGCCTCTGCCCCCCACCCC CAGGAAGGTTCTTAAAGAAGTCAGGGTGCAGGGTGAGAACAACGTAAGCCTCTGCCCCCCACCCC A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63275531..63275678 26863196 MeRIP-seq:(Medium) rs756094701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1932843,Human_RBP_ID_5423923,Human_RBP_ID_7019941,Human_RBP_ID_14166338,Human_RBP_ID_23915861 Human_Splice_Rec_2102778,Human_Splice_Rec_2102779,Human_Splice_Rec_2102802,Human_Splice_Rec_2102803,Human_Splice_Rec_2102826,Human_Splice_Rec_2102827,Human_Splice_Rec_2102832,Human_Splice_Rec_2102833,Human_Splice_Rec_2102856,Human_Splice_Rec_2102857,Human_Splice_Rec_2102862,Human_Splice_Rec_2102863,Human_Splice_Rec_2102884,Human_Splice_Rec_2102892,Human_Splice_Rec_2102893,Human_Splice_Rec_2102916,Human_Splice_Rec_2102917,Human_Splice_Rec_2102938,Human_Splice_Rec_2102939,Human_Splice_Rec_2102948,Human_Splice_Rec_2102949,Human_Splice_Rec_2102964,Human_Splice_Rec_2102965,Human_Splice_Rec_2102990,Human_Splice_Rec_2102991,Human_Splice_Rec_2103012,Human_Splice_Rec_2103013,Human_Splice_Rec_2103038,Human_Splice_Rec_2103039,Human_Splice_Rec_2103058,Human_Splice_Rec_2103059 RMVar_hsa_circ_53220,RMVar_hsa_circ_94309,RMVar_hsa_circ_211300,RMVar_hsa_circ_367891,RMVar_hsa_circ_12971 83560 RMVar_ID_83560 Human_SNP_ID_686960230 m1A Human chr20 + 63278225 63278225 63278225 TCCTATCAAGGGTAAGGACTTGAGAGCTGGGGACGCCTGGCGTGGGCCAGGCCCACAGGGTTCAG TCCTATCAAGGGTAAGGACTTGAGAGCTGGGGGCGCCTGGCGTGGGCCAGGCCCACAGGGTTCAG A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63278176..63278350 26863196 MeRIP-seq:(Medium) rs769160674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924218,Human_RBP_ID_5382794,Human_RBP_ID_19107081,Human_RBP_ID_22601557 RMVar_hsa_circ_94309,RMVar_hsa_circ_211300,RMVar_hsa_circ_12971,RMVar_hsa_circ_211301,RMVar_hsa_circ_125696 83561 RMVar_ID_83561 Human_SNP_ID_686962566 m1A Human chr20 + 63284918 63284918 63284918 CCTGAACGAGAACGTCCTCAAGCCTGCGCAGGAGAAGGTAACGGGCAGCTCCGGGTGGTTGTGCC CCTGAACGAGAACGTCCTCAAGCCTGCGCAGGGGAAGGTAACGGGCAGCTCCGGGTGGTTGTGCC A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63284588..63284940 26863196 MeRIP-seq:(Medium) rs202096342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19006407,Human_RBP_ID_23115492,Human_RBP_ID_27840598 Human_Splice_Rec_2102794,Human_Splice_Rec_2102795,Human_Splice_Rec_2102816,Human_Splice_Rec_2102817,Human_Splice_Rec_2102848,Human_Splice_Rec_2102849,Human_Splice_Rec_2102876,Human_Splice_Rec_2102877,Human_Splice_Rec_2102908,Human_Splice_Rec_2102909,Human_Splice_Rec_2102930,Human_Splice_Rec_2102931,Human_Splice_Rec_2102980,Human_Splice_Rec_2102981,Human_Splice_Rec_2103006,Human_Splice_Rec_2103007,Human_Splice_Rec_2103030,Human_Splice_Rec_2103031,Human_Splice_Rec_2103054,Human_Splice_Rec_2103055,Human_Splice_Rec_2103065,Human_Splice_Rec_2103072,Human_Splice_Rec_2103073,Human_Splice_Rec_2103080,Human_Splice_Rec_2103081,Human_Splice_Rec_2103083 RMVar_hsa_circ_12971,RMVar_hsa_circ_54411 83562 RMVar_ID_83562 Human_SNP_ID_686962844 m1A Human chr20 + 63285665 63285665 63285665 CCGCTGTCTTCATCCGTGCAGGTGAAGGAGGGAAAGATTTTTGATGATGTCTCCAGTGGGGTCTC CCGCTGTCTTCATCCGTGCAGGTGAAGGAGGGGAAGATTTTTGATGATGTCTCCAGTGGGGTCTC A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63285636..63285737 26863196 MeRIP-seq:(Medium) rs1485802807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19006409,Human_RBP_ID_24560962,Human_RBP_ID_25627351 Human_Splice_Rec_2102796,Human_Splice_Rec_2102797,Human_Splice_Rec_2102818,Human_Splice_Rec_2102819,Human_Splice_Rec_2102850,Human_Splice_Rec_2102851,Human_Splice_Rec_2102878,Human_Splice_Rec_2102879,Human_Splice_Rec_2102886,Human_Splice_Rec_2102887,Human_Splice_Rec_2102910,Human_Splice_Rec_2102911,Human_Splice_Rec_2102932,Human_Splice_Rec_2102933,Human_Splice_Rec_2102982,Human_Splice_Rec_2102983,Human_Splice_Rec_2103008,Human_Splice_Rec_2103009,Human_Splice_Rec_2103032,Human_Splice_Rec_2103033,Human_Splice_Rec_2103056,Human_Splice_Rec_2103066,Human_Splice_Rec_2103067,Human_Splice_Rec_2103074,Human_Splice_Rec_2103075,Human_Splice_Rec_2103082,Human_Splice_Rec_2103084 RMVar_hsa_circ_12971,RMVar_hsa_circ_54411 83563 RMVar_ID_83563 Human_SNP_ID_686963652 m1A Human chr20 + 63287676 63287676 63287676 CCTTTGGAAGTGCTGAGCCCACCAAGACCCGCAAGTCCCCGAGCAGCGACAGCTGGACGTGCGCG CCTTTGGAAGTGCTGAGCCCACCAAGACCCGCGAGTCCCCGAGCAGCGACAGCTGGACGTGCGCG A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63287544..63288137 26863196 MeRIP-seq:(Medium) rs1328251437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529247,Human_RBP_ID_9391193,Human_RBP_ID_19004750,Human_RBP_ID_23004815,Human_RBP_ID_27488346 Human_Splice_Rec_2103093 83564 RMVar_ID_83564 Human_SNP_ID_686964171 m1A Human chr20 - 63288839 63288839 63288839 CATGCATGGCTGGCCAAGACTGAGGGTCACACAGGGCAGACAAGGGAGACGAGTCACACGTGGCA CATGCATGGCTGGCCAAGACTGAGGGTCACACGGGGCAGACAAGGGAGACGAGTCACACGTGGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:63288676..63288900 26863196 MeRIP-seq:(Medium) rs1348276346 Functional Loss SNV dbSNP153 33..33 33 - - - 83565 RMVar_ID_83565 Human_SNP_ID_686964464 m1A Human chr20 + 63289686 63289686 63289686 GGTGATGGCCTTTCCCTTCTGCAGGTGCGGGCAGGTGGGCCTGGGACCGGTGCTGGGGCCTCTCC GGTGATGGCCTTTCCCTTCTGCAGGTGCGGGCGGGTGGGCCTGGGACCGGTGCTGGGGCCTCTCC A G ARFGAP1 Ensembl:ENSG00000101199 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63289636..63289739 26863196 MeRIP-seq:(Medium) rs1340126576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568549,Human_RBP_ID_5529265,Human_RBP_ID_7019959,Human_RBP_ID_22081783,Human_RBP_ID_22371439,Human_RBP_ID_26493232,Human_RBP_ID_27488401 Human_Splice_Rec_2103092 Human_miRNA_ID_928554 83566 RMVar_ID_83566 Human_SNP_ID_687016692 m1A Human chr20 + 63442874 63442872 63442875 CCATCACCATCACCACCACCATCACCATCACCATTATCACCACCACCATCACCACCATCACCACC CCATCACCATCACCACCACCATCACCATCAC___TATCACCACCACCATCACCACCATCACCACC CCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63442864..63442995 26863196 MeRIP-seq:(Medium) rs1568934925 Functional Loss DEL dbSNP153 32..34 33 - - - 83567 RMVar_ID_83567 Human_SNP_ID_687016698 m1A Human chr20 + 63442874 63442874 63442874 CCATCACCATCACCACCACCATCACCATCACCATTATCACCACCACCATCACCACCATCACCACC CCATCACCATCACCACCACCATCACCATCACCCTTATCACCACCACCATCACCACCATCACCACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63442864..63442995 26863196 MeRIP-seq:(Medium) rs935033581 Functional Loss SNV dbSNP153 33..33 33 - - - 83568 RMVar_ID_83568 Human_SNP_ID_687030966 m1A Human chr20 + 63486991 63486953 63486991 GCATCCTCAGGGAGCCTGCCCACCCTCCACCCAGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC _________________________________GACCCTCCTCTGCATCCTCAGGGAAGCTGCCC TCCTCCGCATCCTCAGGGAGCCTGCCCACCCTCCACCCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63486990..63487073 26863196 MeRIP-seq:(Medium) rs1568993363 Functional Loss DEL dbSNP153 1..33 33 - - - 83569 RMVar_ID_83569 Human_SNP_ID_687030991 m1A Human chr20 + 63486991 63486990 63486991 GCATCCTCAGGGAGCCTGCCCACCCTCCACCCAGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC GCATCCTCAGGGAGCCTGCCCACCCTCCACCC_GACCCTCCTCTGCATCCTCAGGGAAGCTGCCC CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63486990..63487073 26863196 MeRIP-seq:(Medium) rs1331673863 Functional Loss DEL dbSNP153 33..33 33 - - - 83570 RMVar_ID_83570 Human_SNP_ID_687030992 m1A Human chr20 + 63486991 63486991 63486991 GCATCCTCAGGGAGCCTGCCCACCCTCCACCCAGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC GCATCCTCAGGGAGCCTGCCCACCCTCCACCCCGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63486990..63487073 26863196 MeRIP-seq:(Medium) rs113522989 Functional Loss SNV dbSNP153 33..33 33 - - - 83571 RMVar_ID_83571 Human_SNP_ID_687030993 m1A Human chr20 + 63486991 63486991 63486991 GCATCCTCAGGGAGCCTGCCCACCCTCCACCCAGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC GCATCCTCAGGGAGCCTGCCCACCCTCCACCCTGACCCTCCTCTGCATCCTCAGGGAAGCTGCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63486990..63487073 26863196 MeRIP-seq:(Medium) rs113522989 Functional Loss SNV dbSNP153 33..33 33 - - - 83572 RMVar_ID_83572 Human_SNP_ID_687031458 m1A Human chr20 + 63488205 63488205 63488205 GACATGCGCCTGGCGGGGGTGCGGGGCGCCGGACCGGCGCGCGGGGCGGGGGCGGGGCGGGGGCC GACATGCGCCTGGCGGGGGTGCGGGGCGCCGGGCCGGCGCGCGGGGCGGGGGCGGGGCGGGGGCC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:63488138..63488355 26863410 MeRIP-seq:(Medium) rs1185729856 Functional Loss SNV dbSNP153 33..33 33 - - - 83573 RMVar_ID_83573 Human_SNP_ID_687031578 m1A Human chr20 - 63488427 63488426 63488427 CGGCCCCGCCCACACGCCGCCCCCCGCCCCCCAGGCCGCTTCGCCGTGCGCGACATGAGGCAGAC CGGCCCCGCCCACACGCCGCCCCCCGCCCCCC_GGCCGCTTCGCCGTGCGCGACATGAGGCAGAC CT C EEF1A2 Ensembl:ENSG00000101210 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:63488401..63488450 32194978 MeRIP-seq:(Medium) rs750253697 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_63495 Human_Splice_Rec_2103935 83574 RMVar_ID_83574 Human_SNP_ID_687031798 m1A Human chr20 - 63489052 63489052 63489052 CCACATCGCCTGCAAGTTTGCGGAGCTGAAGGAGAAGATTGACCGGCGCTCTGGCAAGAAGCTGG CCACATCGCCTGCAAGTTTGCGGAGCTGAAGGGGAAGATTGACCGGCGCTCTGGCAAGAAGCTGG T C EEF1A2 Ensembl:ENSG00000101210 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:63489026..63489216 26863196 MeRIP-seq:(Medium) rs756386330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63496,Human_RBP_ID_568642,Human_RBP_ID_23916033,Human_RBP_ID_27488433 83575 RMVar_ID_83575 Human_SNP_ID_687031799 m1A Human chr20 - 63489052 63489052 63489052 CCACATCGCCTGCAAGTTTGCGGAGCTGAAGGAGAAGATTGACCGGCGCTCTGGCAAGAAGCTGG CCACATCGCCTGCAAGTTTGCGGAGCTGAAGGCGAAGATTGACCGGCGCTCTGGCAAGAAGCTGG T G EEF1A2 Ensembl:ENSG00000101210 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:63489026..63489216 26863196 MeRIP-seq:(Medium) rs756386330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63496,Human_RBP_ID_568642,Human_RBP_ID_23916033,Human_RBP_ID_27488433 83576 RMVar_ID_83576 Human_SNP_ID_687034930 m1A Human chr20 - 63497800 63497800 63497800 TCACTGCAGCCCCCCTCGCCCTGAGCCAGAGCACCCCGGGTCCCGCCAGCCCCTCACACTCCCAG TCACTGCAGCCCCCCTCGCCCTGAGCCAGAGCCCCCCGGGTCCCGCCAGCCCCTCACACTCCCAG T G EEF1A2 Ensembl:ENSG00000101210 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63497569..63499300 26863196 MeRIP-seq:(Medium) rs966647711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63501,Human_RBP_ID_244774,Human_RBP_ID_568657,Human_RBP_ID_779778,Human_RBP_ID_4660000,Human_RBP_ID_27488449 Human_Splice_Rec_2103908,Human_Splice_Rec_2103922,Human_Splice_Rec_2103950,Human_Splice_Rec_2103960 83577 RMVar_ID_83577 Human_SNP_ID_687035393 m1A Human chr20 + 63499209 63499209 63499209 TGCGGAACCGCGCGGGAGGGGGCGGGGCGCGGACGCGCGCGGGCGGGCGCCACGGGGACGCGAGG TGCGGAACCGCGCGGGAGGGGGCGGGGCGCGGGCGCGCGCGGGCGGGCGCCACGGGGACGCGAGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63497776..63499275 26863410 MeRIP-seq:(Medium) rs1290376646 Functional Loss SNV dbSNP153 33..33 33 - - - 83578 RMVar_ID_83578 Human_SNP_ID_687041665 m1A Human chr20 + 63520818 63520751 63520818 CGTGGCGCGGCTTCCCGCGGTCTTCTCTGCAAATGGGCTCCGTGGCCTAGCGCCCCCGTCCCCGC _________________________________TGGGCTCCGTGGCCTAGCGCCCCCGTCCCCGC GTCCGCGCGTGCGCACCCCGCGCGCGCCTCTCTGTCGTGGCGCGGCTTCCCGCGGTCTTCTCTGCAAA G PPDPF Ensembl:ENSG00000125534 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63520751..63520970 26863196 MeRIP-seq:(Medium) rs1569004777 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_568661,Human_RBP_ID_778461,Human_RBP_ID_1380800,Human_RBP_ID_4657300,Human_RBP_ID_5119443,Human_RBP_ID_5132287,Human_RBP_ID_5323058,Human_RBP_ID_5445882,Human_RBP_ID_5472120,Human_RBP_ID_9331684,Human_RBP_ID_17086375,Human_RBP_ID_17282617,Human_RBP_ID_17396666,Human_RBP_ID_17572318,Human_RBP_ID_18193703,Human_RBP_ID_18951861,Human_RBP_ID_22533632,Human_RBP_ID_26494230,Human_RBP_ID_27024417,Human_RBP_ID_27299821,Human_RBP_ID_27488451 Human_Splice_Rec_2103963,Human_Splice_Rec_2103965,Human_Splice_Rec_2103971,Human_Splice_Rec_2103975 RMVar_hsa_circ_89309,RMVar_hsa_circ_109010,RMVar_hsa_circ_127425,RMVar_hsa_circ_106053,RMVar_hsa_circ_211314,RMVar_hsa_circ_211316,RMVar_hsa_circ_211317,RMVar_hsa_circ_211315 83579 RMVar_ID_83579 Human_SNP_ID_687041764 m1A Human chr20 + 63520870 63520870 63520870 CCCCCGTCCCCGCCACCCGTGATCGTGCGCCGAGGCCCGCGAGGGGTCGCCGCCCAGGTGAGGGG CCCCCGTCCCCGCCACCCGTGATCGTGCGCCGGGGCCCGCGAGGGGTCGCCGCCCAGGTGAGGGG A G PPDPF Ensembl:ENSG00000125534 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:63520726..63521625;chr20:63520781..63520883 26863410 MeRIP-seq:(Medium) rs1417376779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244404,Human_RBP_ID_568664,Human_RBP_ID_778461,Human_RBP_ID_4660004,Human_RBP_ID_5119443,Human_RBP_ID_5132287,Human_RBP_ID_5323058,Human_RBP_ID_9331684,Human_RBP_ID_17086517,Human_RBP_ID_17396667,Human_RBP_ID_17572318,Human_RBP_ID_18193705,Human_RBP_ID_18951862,Human_RBP_ID_26821100 Human_Splice_Rec_2103963,Human_Splice_Rec_2103965,Human_Splice_Rec_2103971,Human_Splice_Rec_2103975 Human_miRNA_ID_2018123 RMVar_hsa_circ_89309,RMVar_hsa_circ_109010,RMVar_hsa_circ_127425,RMVar_hsa_circ_106053,RMVar_hsa_circ_211314,RMVar_hsa_circ_211316,RMVar_hsa_circ_211317,RMVar_hsa_circ_211315 83580 RMVar_ID_83580 Human_SNP_ID_687041933 m1A Human chr20 - 63521337 63521337 63521337 ACTCACGCCGGTAGTAGTCGTGGGTGGCCACGAGCGAGCCGCTGGAGGGGATGGCCGCCATGCTT ACTCACGCCGGTAGTAGTCGTGGGTGGCCACGGGCGAGCCGCTGGAGGGGATGGCCGCCATGCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63521254..63521385 26863196 MeRIP-seq:(Medium) rs1487398907 Functional Loss SNV dbSNP153 33..33 33 - - - 83581 RMVar_ID_83581 Human_SNP_ID_687042052 m1A Human chr20 - 63521518 63521518 63521518 TGCTGCAGGAGCTGTTGCTGGAAGTGGAACCCAGGCGGCCTGGAGAGGAGAGGTCCCGTCAGCAA TGCTGCAGGAGCTGTTGCTGGAAGTGGAACCCGGGCGGCCTGGAGAGGAGAGGTCCCGTCAGCAA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63521501..63521550 26863196 MeRIP-seq:(Medium) rs201721055 Functional Loss SNV dbSNP153 33..33 33 - - - 83582 RMVar_ID_83582 Human_SNP_ID_687042172 m1A Human chr20 + 63521692 63521692 63521692 TCTCTCAGGTCTCCCCAAGGCTGACCCGGGTCATTGGTGGGCCAGCTTCTTTTTCGGGAAGTCCA TCTCTCAGGTCTCCCCAAGGCTGACCCGGGTCGTTGGTGGGCCAGCTTCTTTTTCGGGAAGTCCA A G PPDPF Ensembl:ENSG00000125534 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63521501..63521950 26863196 MeRIP-seq:(Medium) rs766832150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568672,Human_RBP_ID_4657310,Human_RBP_ID_5423928,Human_RBP_ID_5445883,Human_RBP_ID_17975719,Human_RBP_ID_18444713,Human_RBP_ID_18951863,Human_RBP_ID_25625048,Human_RBP_ID_26821113,Human_RBP_ID_27299828 Human_Splice_Rec_2103970,Human_Splice_Rec_2103978 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83583 RMVar_ID_83583 Human_SNP_ID_687042302 m1A Human chr20 + 63521897 63521897 63521897 GGGCCCCCGTCCTGACCTGAGCGGTTACCACCAGCCCCAGGCCTGCGGAGGCGCTAGTCCACCAG GGGCCCCCGTCCTGACCTGAGCGGTTACCACCGGCCCCAGGCCTGCGGAGGCGCTAGTCCACCAG A G PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:63521676..63522100 26863410 MeRIP-seq:(Medium) rs1160918821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568679,Human_RBP_ID_18193714,Human_RBP_ID_23916046,Human_RBP_ID_26494233 Human_miRNA_ID_2052976 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83584 RMVar_ID_83584 Human_SNP_ID_687042338 m1A Human chr20 - 63521946 63521946 63521946 GGGGAGGGGGGCGAGGGATGCGGAGTGGGGAGAGGGGCGGGGAGGGGCTCTGGTGGACTAGCGCC GGGGAGGGGGGCGAGGGATGCGGAGTGGGGAGGGGGGCGGGGAGGGGCTCTGGTGGACTAGCGCC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:63521855..63521953 26863410 MeRIP-seq:(Medium) rs754893938 Functional Loss SNV dbSNP153 33..33 33 - - - 83585 RMVar_ID_83585 Human_SNP_ID_687042342 m1A Human chr20 + 63521960 63521952 63521961 AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGCATCCCTCGCCCCCCTCCCCACCTCCCACCCCCC AGAGCCCCTCCCCGCCCCTCTCCCC_________CCCTCGCCCCCCTCCCCACCTCCCACCCCCC CACTCCGCAT C PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:63521861..63521968 26863410 MeRIP-seq:(Medium) rs751250456 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_568680,Human_RBP_ID_17086983,Human_RBP_ID_18950970 Human_miRNA_ID_2368441,Human_miRNA_ID_2726753 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83586 RMVar_ID_83586 Human_SNP_ID_687042342 m1A Human chr20 - 63521961 63521952 63521961 TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGGATGCGGAGTGGGGAGAGGGGCGGGGAGGGGCTC TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGG_________GGGGAGAGGGGCGGGGAGGGGCTC CACTCCGCAT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:63521701..63522075 32194978 MeRIP-seq:(Medium) rs751250456 Functional Loss DEL dbSNP153 33..41 33 - - - 83587 RMVar_ID_83587 Human_SNP_ID_687042347 m1A Human chr20 + 63521960 63521957 63521961 AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGCATCCCTCGCCCCCCTCCCCACCTCCCACCCCCC AGAGCCCCTCCCCGCCCCTCTCCCCACTCC____CCCTCGCCCCCCTCCCCACCTCCCACCCCCC CGCAT C PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:63521861..63521968 26863410 MeRIP-seq:(Medium) rs757733692 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_568680,Human_RBP_ID_17086983,Human_RBP_ID_18950970 Human_miRNA_ID_2368441,Human_miRNA_ID_2726753 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83588 RMVar_ID_83588 Human_SNP_ID_687042347 m1A Human chr20 - 63521961 63521957 63521961 TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGGATGCGGAGTGGGGAGAGGGGCGGGGAGGGGCTC TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGG____GGAGTGGGGAGAGGGGCGGGGAGGGGCTC CGCAT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:63521701..63522075 32194978 MeRIP-seq:(Medium) rs757733692 Functional Loss DEL dbSNP153 33..36 33 - - - 83589 RMVar_ID_83589 Human_SNP_ID_687042351 m1A Human chr20 + 63521960 63521959 63521961 AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGCATCCCTCGCCCCCCTCCCCACCTCCCACCCCCC AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGC__CCCTCGCCCCCCTCCCCACCTCCCACCCCCC CAT C PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:63521861..63521968 26863410 MeRIP-seq:(Medium) rs1477149031 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_568680,Human_RBP_ID_17086983,Human_RBP_ID_18950970 Human_miRNA_ID_2368441,Human_miRNA_ID_2726753 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83590 RMVar_ID_83590 Human_SNP_ID_687042351 m1A Human chr20 - 63521961 63521959 63521961 TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGGATGCGGAGTGGGGAGAGGGGCGGGGAGGGGCTC TGGGGGGTGGGAGGTGGGGAGGGGGGCGAGGG__GCGGAGTGGGGAGAGGGGCGGGGAGGGGCTC CAT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:63521701..63522075 32194978 MeRIP-seq:(Medium) rs1477149031 Functional Loss DEL dbSNP153 33..34 33 - - - 83591 RMVar_ID_83591 Human_SNP_ID_687042352 m1A Human chr20 + 63521960 63521960 63521960 AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGCATCCCTCGCCCCCCTCCCCACCTCCCACCCCCC AGAGCCCCTCCCCGCCCCTCTCCCCACTCCGCCTCCCTCGCCCCCCTCCCCACCTCCCACCCCCC A C PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:63521861..63521968 26863410 MeRIP-seq:(Medium) rs1167871058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568680,Human_RBP_ID_17086983,Human_RBP_ID_18950970 Human_miRNA_ID_2368441,Human_miRNA_ID_2726753 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83592 RMVar_ID_83592 Human_SNP_ID_687042435 m1A Human chr20 + 63522050 63522049 63522050 AAGCAGACCTTCGCATCAACACAGCAGACACCAAAAACCAGTGAGAGCCCCGCTCTCTACCGCCC AAGCAGACCTTCGCATCAACACAGCAGACACC_AAAACCAGTGAGAGCCCCGCTCTCTACCGCCC CA C PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63522001..63522175 26863196 MeRIP-seq:(Medium) rs1157846805 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_568682,Human_RBP_ID_4665860,Human_RBP_ID_17086376,Human_RBP_ID_17282618,Human_RBP_ID_17396672,Human_RBP_ID_17512692,Human_RBP_ID_17571309,Human_RBP_ID_17659477,Human_RBP_ID_26492541,Human_RBP_ID_27299832 Human_miRNA_ID_184386,Human_miRNA_ID_3066478 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83593 RMVar_ID_83593 Human_SNP_ID_687042447 m1A Human chr20 + 63522076 63522076 63522076 GACACCAAAAACCAGTGAGAGCCCCGCTCTCTACCGCCCGGCCCCAGCACTCGCTAGCTTTCCTG GACACCAAAAACCAGTGAGAGCCCCGCTCTCTGCCGCCCGGCCCCAGCACTCGCTAGCTTTCCTG A G PPDPF Ensembl:ENSG00000125534 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63522030..63522113 26863196 MeRIP-seq:(Medium) rs1314882757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568686,Human_RBP_ID_5132290,Human_RBP_ID_17086519,Human_RBP_ID_17282618,Human_RBP_ID_17396673,Human_RBP_ID_17512912,Human_RBP_ID_17571309,Human_RBP_ID_17659477,Human_RBP_ID_23916048,Human_RBP_ID_26821645,Human_RBP_ID_27299832 Human_miRNA_ID_1166587,Human_miRNA_ID_2686506,Human_miRNA_ID_2775927 RMVar_hsa_circ_106053,RMVar_hsa_circ_211317 83594 RMVar_ID_83594 Human_SNP_ID_687046082 m1A Human chr20 - 63532124 63532123 63532125 ACACTGATCCAGACACACACACAGACACACACAGATCACATTGGCTCAAAGACTTCATCCTCTCT ACACTGATCCAGACACACACACAGACACACA__GATCACATTGGCTCAAAGACTTCATCCTCTCT CTG C PTK6 Ensembl:ENSG00000101213 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63532119..63532252 26863196 MeRIP-seq:(Medium) rs1423640588 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2693577 RMVar_hsa_circ_211319,RMVar_hsa_circ_86063 83595 RMVar_ID_83595 Human_SNP_ID_687047947 m1A Human chr20 - 63536195 63536195 63536195 CTGAGAACTCGCCCAGGTGAGAAGTGGGGAGGAGGCCAGGTGAGGAGGGGGTGGGAGGCCAGGTG CTGAGAACTCGCCCAGGTGAGAAGTGGGGAGGGGGCCAGGTGAGGAGGGGGTGGGAGGCCAGGTG T C PTK6 Ensembl:ENSG00000101213 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63536187..63536410 26863196 MeRIP-seq:(Medium) rs1158561468 Functional Loss SNV dbSNP153 33..33 33 - - - 83596 RMVar_ID_83596 Human_SNP_ID_687048223 m1A Human chr20 - 63537033 63537033 63537033 GGGAGCTTTGGCACAGGCCACCCTCTAGGCACAGGGGAGGGACAGGGCTCTGGGCTGCTCAGGGA GGGAGCTTTGGCACAGGCCACCCTCTAGGCACGGGGGAGGGACAGGGCTCTGGGCTGCTCAGGGA T C PTK6 Ensembl:ENSG00000101213 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63537021..63537331 26863196 MeRIP-seq:(Medium) rs1424530856 Functional Loss SNV dbSNP153 33..33 33 - - - 83597 RMVar_ID_83597 Human_SNP_ID_687055796 m1A Human chr20 - 63559227 63559227 63559227 CTATGCCTTCCTGAAGAGCCCTCTCCACCTGCAAGGTGCCAGGACTGGGAGGGAAAGTCCAGGGC CTATGCCTTCCTGAAGAGCCCTCTCCACCTGCCAGGTGCCAGGACTGGGAGGGAAAGTCCAGGGC T G HELZ2 Ensembl:ENSG00000130589 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63559082..63559989 32194978 MeRIP-seq:(Medium) rs983131222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211320,RMVar_hsa_circ_119617,RMVar_hsa_circ_122266,RMVar_hsa_circ_211321 83598 RMVar_ID_83598 Human_SNP_ID_687057000 m1A Human chr20 - 63561386 63561386 63561386 GTCGGAAATCAAGGCCTTTGACACCCGGCTGCAGAGAGGGGAGCTCTTCTCCAGGGAGGACCTGG GTCGGAAATCAAGGCCTTTGACACCCGGCTGCTGAGAGGGGAGCTCTTCTCCAGGGAGGACCTGG T A HELZ2 Ensembl:ENSG00000130589 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63561261..63562083 32194978 MeRIP-seq:(Medium) rs1343677441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17975735 Human_Splice_Rec_2104036,Human_Splice_Rec_2104037,Human_Splice_Rec_2104050,Human_Splice_Rec_2104051,Human_Splice_Rec_2104080,Human_Splice_Rec_2104081 RMVar_hsa_circ_211320,RMVar_hsa_circ_119617,RMVar_hsa_circ_211322,RMVar_hsa_circ_76546 83599 RMVar_ID_83599 Human_SNP_ID_687058384 m1A Human chr20 + 63564095 63564094 63564095 CGCCGTGCAGGTGGTGGCCGAGGTGCAGTGACAGGGGCACCCGGTCCCCATGCTTCTCACACAGG CGCCGTGCAGGTGGTGGCCGAGGTGCAGTGAC_GGGGCACCCGGTCCCCATGCTTCTCACACAGG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63563999..63564448 32194978 MeRIP-seq:(Medium) rs1342948720 Functional Loss DEL dbSNP153 33..33 33 - - - 83600 RMVar_ID_83600 Human_SNP_ID_687059935 m1A Human chr20 + 63567088 63567088 63567088 TGGCGTGGATGGGGTTGCCCTTGGCCACGTAGAAGTGCCGCGAGATGAAGCTGACAATGGCGTCC TGGCGTGGATGGGGTTGCCCTTGGCCACGTAGCAGTGCCGCGAGATGAAGCTGACAATGGCGTCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63564547..63567676 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 83601 RMVar_ID_83601 Human_SNP_ID_687060486 m1A Human chr20 + 63568480 63568480 63568480 CCAAAGGGGCCATAGATGAGTAGCGGGGGGACACGCCTCCCATCCCCAGGGCCCCAGCCCGCGAT CCAAAGGGGCCATAGATGAGTAGCGGGGGGACTCGCCTCCCATCCCCAGGGCCCCAGCCCGCGAT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63568407..63569653 32194978 MeRIP-seq:(Medium) rs1431349527 Functional Loss SNV dbSNP153 33..33 33 - - - 83602 RMVar_ID_83602 Human_SNP_ID_687066937 m1A Human chr20 - 63589705 63589702 63589705 CCAGGTGCCGAGCGCGACCCTGCAGGTGCTGGACGCGGTGCAGCAGGTCACGAGGCCCCCATGTC CCAGGTGCCGAGCGCGACCCTGCAGGTGCTGG___CGGTGCAGCAGGTCACGAGGCCCCCATGTC GCGT G GMEB2 Ensembl:ENSG00000101216 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63589675..63589768 26863196 MeRIP-seq:(Medium) rs1284198317 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_101160,RMVar_hsa_circ_211325 83603 RMVar_ID_83603 Human_SNP_ID_687066941 m1A Human chr20 - 63589705 63589704 63589706 CCAGGTGCCGAGCGCGACCCTGCAGGTGCTGGACGCGGTGCAGCAGGTCACGAGGCCCCCATGTC CCAGGTGCCGAGCGCGACCCTGCAGGTGCTG__CGCGGTGCAGCAGGTCACGAGGCCCCCATGTC GTC G GMEB2 Ensembl:ENSG00000101216 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63589675..63589768 26863196 MeRIP-seq:(Medium) rs1414643289 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_101160,RMVar_hsa_circ_211325 83604 RMVar_ID_83604 Human_SNP_ID_687067011 m1A Human chr20 - 63589965 63589964 63589966 GGGCAGGTGGGTCACGTGGTCTGCAGAACCAAAGAGAGGAATCGCCAAAACAAATCACGAGAAGA GGGCAGGTGGGTCACGTGGTCTGCAGAACCA__GAGAGGAATCGCCAAAACAAATCACGAGAAGA CTT C GMEB2 Ensembl:ENSG00000101216 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63589914..63590068 26863196 MeRIP-seq:(Medium) rs908031665 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9885,Human_RBP_ID_14166962,Human_RBP_ID_18777055 RMVar_hsa_circ_101160,RMVar_hsa_circ_211325 83605 RMVar_ID_83605 Human_SNP_ID_687067202 m1A Human chr20 + 63590409 63590409 63590409 GGCCAAGACTGTGTATCCCCCGAGCAGCGGGGAGGCCGGGGAGCTGGCGGGGGGCGCCTGAAGGG GGCCAAGACTGTGTATCCCCCGAGCAGCGGGGCGGCCGGGGAGCTGGCGGGGGGCGCCTGAAGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63590360..63590663 26863196 MeRIP-seq:(Medium) rs1475341422 Functional Loss SNV dbSNP153 33..33 33 - - - 83606 RMVar_ID_83606 Human_SNP_ID_687067209 m1A Human chr20 - 63590421 63590421 63590421 TGGGCAAGGGTTCCCTTCAGGCGCCCCCCGCCAGCTCCCCGGCCTCCCCGCTGCTCGGGGGATAC TGGGCAAGGGTTCCCTTCAGGCGCCCCCCGCCGGCTCCCCGGCCTCCCCGCTGCTCGGGGGATAC T C GMEB2 Ensembl:ENSG00000101216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63590370..63590448 26863196 MeRIP-seq:(Medium) rs1416892016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22260736 Human_miRNA_ID_2147550,Human_miRNA_ID_2988977,Human_miRNA_ID_3022679 RMVar_hsa_circ_101160,RMVar_hsa_circ_211325 83607 RMVar_ID_83607 Human_SNP_ID_687071464 m1A Human chr20 - 63604825 63604825 63604825 TCCCTTCACTTCACCAGGGGCGACCTGACGGAAGATAACATGGAGACAGAAAATGCAGCGGCAGC TCCCTTCACTTCACCAGGGGCGACCTGACGGATGATAACATGGAGACAGAAAATGCAGCGGCAGC T A GMEB2 Ensembl:ENSG00000101216 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:63604806..63604934 26863196 MeRIP-seq:(Medium) rs1412529326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926294,Human_RBP_ID_19004751,Human_RBP_ID_25627352 Human_Splice_Rec_2104105,Human_Splice_Rec_2104120,Human_Splice_Rec_2104121,Human_Splice_Rec_2104138,Human_Splice_Rec_2104139 RMVar_hsa_circ_46540,RMVar_hsa_circ_101160,RMVar_hsa_circ_211325,RMVar_hsa_circ_12895,RMVar_hsa_circ_284008,RMVar_hsa_circ_376558,RMVar_hsa_circ_211326,RMVar_hsa_circ_14457 83608 RMVar_ID_83608 Human_SNP_ID_687078315 m1A Human chr20 - 63627011 63626985 63627012 CCGCGGCCGCCGCCGCCGCCCGCCGCCGCCGCAGCTCCCGACGCCGCCGCCCCCGCCGGGTGCCT CCGCGGCCGCCGCCGCCGCCCGCCGCCGCCG___________________________GGTGCCT CCGGCGGGGGCGGCGGCGTCGGGAGCTG C GMEB2 Ensembl:ENSG00000101216 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63619862..63627119 26863196 MeRIP-seq:(Medium) rs1376607352 Functional Loss DEL dbSNP153 32..58 33 - - - Human_RBP_ID_4665869 Human_Splice_Rec_2104135 83609 RMVar_ID_83609 Human_SNP_ID_687078516 m1A Human chr20 + 63627353 63627353 63627353 CGATGGTCAGTGGACGGACGGCGCCAGGGAGCAGTGCCCACGCGCGGCAGGGCGGTACCTTCAGG CGATGGTCAGTGGACGGACGGCGCCAGGGAGCGGTGCCCACGCGCGGCAGGGCGGTACCTTCAGG A G MHENCR Ensembl:ENSG00000232442 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63627272..63628259 26863196 MeRIP-seq:(Medium) rs905874853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831235,Human_RBP_ID_3657068,Human_RBP_ID_5100648 Human_Splice_Rec_2104153,Human_Splice_Rec_2104155 83610 RMVar_ID_83610 Human_SNP_ID_687078619 m1A Human chr20 + 63627687 63627687 63627687 CACAGCCGACACCCCGATCCCACCCCTGCCCAACAGCCGGCACCCACCCCAATCCCATAGCTAAC CACAGCCGACACCCCGATCCCACCCCTGCCCACCAGCCGGCACCCACCCCAATCCCATAGCTAAC A C MHENCR Ensembl:ENSG00000232442 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63627592..63627704 26863410 MeRIP-seq:(Medium) rs561685163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132293,Human_RBP_ID_8261176,Human_RBP_ID_17086206,Human_RBP_ID_26788671 83611 RMVar_ID_83611 Human_SNP_ID_687078620 m1A Human chr20 + 63627687 63627687 63627687 CACAGCCGACACCCCGATCCCACCCCTGCCCAACAGCCGGCACCCACCCCAATCCCATAGCTAAC CACAGCCGACACCCCGATCCCACCCCTGCCCATCAGCCGGCACCCACCCCAATCCCATAGCTAAC A T MHENCR Ensembl:ENSG00000232442 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63627592..63627704 26863410 MeRIP-seq:(Medium) rs561685163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132293,Human_RBP_ID_8261176,Human_RBP_ID_17086206,Human_RBP_ID_26788671 83612 RMVar_ID_83612 Human_SNP_ID_687078699 m1A Human chr20 - 63627901 63627877 63627901 CGGGGTATCAGCTATGCTATGCGATCGGGGTGAGTGCCGGCTGTGGGATCGGGGTGCCGGCTGCG CGGGGTATCAGCTATGCTATGCGATCGGGGTG________________________CCGGCTGCG GCACCCCGATCCCACAGCCGGCACT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:63627801..63628000 26863410 MeRIP-seq:(Medium) rs1303984180 Functional Loss DEL dbSNP153 33..56 33 - - - 83613 RMVar_ID_83613 Human_SNP_ID_687078711 m1A Human chr20 - 63627901 63627901 63627901 CGGGGTATCAGCTATGCTATGCGATCGGGGTGAGTGCCGGCTGTGGGATCGGGGTGCCGGCTGCG CGGGGTATCAGCTATGCTATGCGATCGGGGTGGGTGCCGGCTGTGGGATCGGGGTGCCGGCTGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:63627801..63628000 26863410 MeRIP-seq:(Medium) rs1165116084 Functional Loss SNV dbSNP153 33..33 33 - - - 83614 RMVar_ID_83614 Human_SNP_ID_687078735 m1A Human chr20 - 63627993 63627962 63627993 GGGGCGGGATCGGGGTGTCATCTATGGGATCGAGGTGCTGGCTATGGGACTGGGGTGGGATCGGG GGGGCGGGATCGGGGTGTCATCTATGGGATCG_______________________________GG CCGATCCCACCCCAGTCCCATAGCCAGCACCT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63627899..63627994 26863410 MeRIP-seq:(Medium) rs1198668305 Functional Loss DEL dbSNP153 33..63 33 - - - 83615 RMVar_ID_83615 Human_SNP_ID_687078745 m1A Human chr20 - 63627993 63627993 63627993 GGGGCGGGATCGGGGTGTCATCTATGGGATCGAGGTGCTGGCTATGGGACTGGGGTGGGATCGGG GGGGCGGGATCGGGGTGTCATCTATGGGATCGGGGTGCTGGCTATGGGACTGGGGTGGGATCGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63627899..63627994 26863410 MeRIP-seq:(Medium) rs568913322 Functional Loss SNV dbSNP153 33..33 33 - - - 83616 RMVar_ID_83616 Human_SNP_ID_687084038 m1A Human chr20 - 63644234 63644234 63644234 CTGCTCCTGCTTCTACACACAGCCGCACCCCAATACCGTCTACCAGTACGGGGGTGAGTGCCTGG CTGCTCCTGCTTCTACACACAGCCGCACCCCAGTACCGTCTACCAGTACGGGGGTGAGTGCCTGG T C STMN3 Ensembl:ENSG00000197457 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:63644201..63644325 32194978 MeRIP-seq:(Medium) rs1259958971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568756,Human_RBP_ID_5472308,Human_RBP_ID_9389726,Human_RBP_ID_19004753 Human_Splice_Rec_2104158,Human_Splice_Rec_2104159,Human_Splice_Rec_2104164,Human_Splice_Rec_2104165,Human_Splice_Rec_2104170,Human_Splice_Rec_2104171,Human_Splice_Rec_2104176,Human_Splice_Rec_2104177,Human_Splice_Rec_2104180,Human_Splice_Rec_2104181 RMVar_hsa_circ_321641 83617 RMVar_ID_83617 Human_SNP_ID_687088581 m1A Human chr20 - 63658379 63658379 63658379 CCGACTCCAGTCGAGGGCCGCCACCCGTCCCCAGCTGTCAGCCAGCTCAGAGTTTTCGCGGGCAG CCGACTCCAGTCGAGGGCCGCCACCCGTCCCCTGCTGTCAGCCAGCTCAGAGTTTTCGCGGGCAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63658331..63658475 26863196 MeRIP-seq:(Medium) rs962756179 Functional Loss SNV dbSNP153 33..33 33 - - - 83618 RMVar_ID_83618 Human_SNP_ID_687092235 m1A Human chr20 + 63668474 63668474 63668474 GAGTAAGCACGTGAGCTGATGATACTGAAGGGAAATAGAGCAGAGGGAGGAGGCGGAGACCGAGC GAGTAAGCACGTGAGCTGATGATACTGAAGGGCAATAGAGCAGAGGGAGGAGGCGGAGACCGAGC A C RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63668464..63668632 26863196 MeRIP-seq:(Medium) rs984442610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14167310,Human_RBP_ID_21984179,Human_RBP_ID_22479223,Human_RBP_ID_22722395 RMVar_hsa_circ_91497,RMVar_hsa_circ_82069,RMVar_hsa_circ_211329,RMVar_hsa_circ_69882,RMVar_hsa_circ_116044,RMVar_hsa_circ_211330,RMVar_hsa_circ_211331,RMVar_hsa_circ_211333,RMVar_hsa_circ_348649 83619 RMVar_ID_83619 Human_SNP_ID_687092277 m1A Human chr20 - 63668613 63668613 63668613 TTCTGCTACAGCTTCCCAGGAGTCGGCCCCCCAGCCGCCCCCACTCACCTCTTCCCTTGCTCTGC TTCTGCTACAGCTTCCCAGGAGTCGGCCCCCCTGCCGCCCCCACTCACCTCTTCCCTTGCTCTGC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63668487..63668616 26863196 MeRIP-seq:(Medium) rs1209205180 Functional Loss SNV dbSNP153 33..33 33 - - - 83620 RMVar_ID_83620 Human_SNP_ID_687095566 m1A Human chr20 + 63678620 63678620 63678620 ACAGCACACACACTCCCACGAACAGCACACACACTCCCACGAACAGCACACACACTCCCACGGAA ACAGCACACACACTCCCACGAACAGCACACACCCTCCCACGAACAGCACACACACTCCCACGGAA A C RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63678573..63678719 26863196 MeRIP-seq:(Medium) rs1371142699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206741 RMVar_hsa_circ_91497,RMVar_hsa_circ_69882,RMVar_hsa_circ_116044,RMVar_hsa_circ_211330,RMVar_hsa_circ_211331,RMVar_hsa_circ_317360,RMVar_hsa_circ_43156,RMVar_hsa_circ_211336,RMVar_hsa_circ_124436,RMVar_hsa_circ_76354,RMVar_hsa_circ_211335 83621 RMVar_ID_83621 Human_SNP_ID_687095567 m1A Human chr20 + 63678620 63678620 63678620 ACAGCACACACACTCCCACGAACAGCACACACACTCCCACGAACAGCACACACACTCCCACGGAA ACAGCACACACACTCCCACGAACAGCACACACTCTCCCACGAACAGCACACACACTCCCACGGAA A T RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63678573..63678719 26863196 MeRIP-seq:(Medium) rs1371142699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206741 RMVar_hsa_circ_91497,RMVar_hsa_circ_69882,RMVar_hsa_circ_116044,RMVar_hsa_circ_211330,RMVar_hsa_circ_211331,RMVar_hsa_circ_317360,RMVar_hsa_circ_43156,RMVar_hsa_circ_211336,RMVar_hsa_circ_124436,RMVar_hsa_circ_76354,RMVar_hsa_circ_211335 83622 RMVar_ID_83622 Human_SNP_ID_687095661 m1A Human chr20 - 63678785 63678741 63678785 GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGGAGAGTGTGCTGTTCCGTGGGAGAGTGTGCCGTT GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGG_________________________________ ACACTCCCACGGAACGGCACACTCTCCCACGGAACAGCACACTCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63678783..63678908 26863196 MeRIP-seq:(Medium) rs1569095786 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_23916174 83623 RMVar_ID_83623 Human_SNP_ID_687095668 m1A Human chr20 - 63678785 63678749 63678785 GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGGAGAGTGTGCTGTTCCGTGGGAGAGTGTGCCGTT GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGG_________________________________ ACGGAACGGCACACTCTCCCACGGAACAGCACACTCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63678783..63678908 26863196 MeRIP-seq:(Medium) rs1370725123 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_23916174 83624 RMVar_ID_83624 Human_SNP_ID_687095696 m1A Human chr20 - 63678785 63678785 63678785 GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGGAGAGTGTGCTGTTCCGTGGGAGAGTGTGCCGTT GTTCCGTGGGAGTGTGTGTGCTGTTCCGTGGGGGAGTGTGCTGTTCCGTGGGAGAGTGTGCCGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63678783..63678908 26863196 MeRIP-seq:(Medium) rs1398186115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23916174 83625 RMVar_ID_83625 Human_SNP_ID_687100110 m1A Human chr20 - 63690376 63690373 63690376 GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAGAAGGGGCCAGGCGACTTGGCCTCGCTGACAGCA GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAG___GGGCCAGGCGACTTGGCCTCGCTGACAGCA CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63690104..63690388 32194978 MeRIP-seq:(Medium) rs771771098 Functional Loss DEL dbSNP153 33..35 33 - - - Clinvar_Rec_432 83626 RMVar_ID_83626 Human_SNP_ID_687100114 m1A Human chr20 - 63690376 63690376 63690376 GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAGAAGGGGCCAGGCGACTTGGCCTCGCTGACAGCA GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAGGAGGGGCCAGGCGACTTGGCCTCGCTGACAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63690104..63690388 32194978 MeRIP-seq:(Medium) rs757763356 Functional Loss SNV dbSNP153 33..33 33 - - - 83627 RMVar_ID_83627 Human_SNP_ID_687101340 m1A Human chr20 - 63692935 63692934 63692936 AGAGGGGGCCGAGACAGGCGGCCAGGGCGGCGAAGTCATCGGAACCCTTGTAGTCCTGCAGGGCC AGAGGGGGCCGAGACAGGCGGCCAGGGCGGC__AGTCATCGGAACCCTTGTAGTCCTGCAGGGCC TTC T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63692792..63692943 32194978 MeRIP-seq:(Medium) rs1568717529 Functional Loss DEL dbSNP153 32..33 33 - - - 83628 RMVar_ID_83628 Human_SNP_ID_687101941 m1A Human chr20 - 63693510 63693453 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGG_________________________________ ACCTCCACCTCCACCTCCACCTCCACCTCCACCACCACCTCCACCTCCACCACCACCT A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1568719895 Functional Loss DEL dbSNP153 33..65 33 - - - 83629 RMVar_ID_83629 Human_SNP_ID_687102025 m1A Human chr20 - 63693510 63693489 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGG_____________________TGGTGGTGGAGG ACCTCCACCTCCACCACCACCT A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1568720278 Functional Loss DEL dbSNP153 33..53 33 - - - 83630 RMVar_ID_83630 Human_SNP_ID_687102036 m1A Human chr20 - 63693510 63693495 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGG_______________TGGAGGTGGTGGTGGAGG ACCTCCACCACCACCT A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1568720322 Functional Loss DEL dbSNP153 33..47 33 - - - 83631 RMVar_ID_83631 Human_SNP_ID_687102052 m1A Human chr20 - 63693510 63693501 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGG_________TGGAGGTGGAGGTGGTGGTGGAGG ACCACCACCT A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1281496330 Functional Loss DEL dbSNP153 33..41 33 - - - 83632 RMVar_ID_83632 Human_SNP_ID_687102059 m1A Human chr20 - 63693510 63693504 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGG______TGGTGGAGGTGGAGGTGGTGGTGGAGG ACCACCT A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1568720423 Functional Loss DEL dbSNP153 33..38 33 - - - 83633 RMVar_ID_83633 Human_SNP_ID_687102071 m1A Human chr20 - 63693510 63693510 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG T A piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1384566118 Functional Loss SNV dbSNP153 33..33 33 - - - 83634 RMVar_ID_83634 Human_SNP_ID_687102072 m1A Human chr20 - 63693510 63693510 63693510 GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGAGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG GGTGGTGGTGGTGGAGGTGGTGGTGGTGGAGGGGGTGGTGGTGGAGGTGGAGGTGGTGGTGGAGG T C piR-36365 RNACentral:URS0000213C1D piRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63693499..63693571 26863196 MeRIP-seq:(Medium) rs1384566118 Functional Loss SNV dbSNP153 33..33 33 - - - 83635 RMVar_ID_83635 Human_SNP_ID_687103513 m1A Human chr20 + 63695388 63695388 63695388 GACCCAGAGCAAGATCTCGTCCTTCCTTAGACAGAGGCCAGCAGGGACTGTGGGGGCGGGCGGTG GACCCAGAGCAAGATCTCGTCCTTCCTTAGACGGAGGCCAGCAGGGACTGTGGGGGCGGGCGGTG A G RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63693180..63696143 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18167808 Human_Splice_Rec_2104246,Human_Splice_Rec_2104247,Human_Splice_Rec_2104312,Human_Splice_Rec_2104313,Human_Splice_Rec_2104384,Human_Splice_Rec_2104448,Human_Splice_Rec_2104449,Human_Splice_Rec_2104584,Human_Splice_Rec_2104602,Human_Splice_Rec_2104662,Human_Splice_Rec_2104663,Human_Splice_Rec_2104700,Human_Splice_Rec_2104701,Human_Splice_Rec_2104728 Human_miRNA_ID_2210970,Human_miRNA_ID_2513397,Human_miRNA_ID_3056216 RMVar_hsa_circ_91497,RMVar_hsa_circ_211330,RMVar_hsa_circ_340566 83636 RMVar_ID_83636 Human_SNP_ID_687104359 m1A Human chr20 + 63697022 63697022 63697022 CCGCGCCACTACACGCAGTTCTGGAACTACCTAGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG CCGCGCCACTACACGCAGTTCTGGAACTACCTGGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG A G RTEL1-TNFRSF6B,TNFRSF6B Ensembl:ENSG00000026036,Ensembl:ENSG00000243509 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63697009..63697156 26863196 MeRIP-seq:(Medium) rs2738787 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_433 GWAS_ID_10089,GWAS_ID_10090,GWAS_ID_10091,GWAS_ID_10092,GWAS_ID_10093,GWAS_ID_10094,GWAS_ID_10095 RMVar_hsa_circ_91497,RMVar_hsa_circ_211330 83637 RMVar_ID_83637 Human_SNP_ID_687104360 m1A Human chr20 + 63697022 63697022 63697022 CCGCGCCACTACACGCAGTTCTGGAACTACCTAGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG CCGCGCCACTACACGCAGTTCTGGAACTACCTTGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG A T RTEL1-TNFRSF6B,TNFRSF6B Ensembl:ENSG00000026036,Ensembl:ENSG00000243509 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63697009..63697156 26863196 MeRIP-seq:(Medium) rs2738787 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_433 GWAS_ID_10089,GWAS_ID_10090,GWAS_ID_10091,GWAS_ID_10092,GWAS_ID_10093,GWAS_ID_10094,GWAS_ID_10095 RMVar_hsa_circ_91497,RMVar_hsa_circ_211330 83638 RMVar_ID_83638 Human_SNP_ID_687104378 m1A Human chr20 - 63697048 63697048 63697048 AAGCCCGTGCCTCCTCCTCACGCTCCCCGCAGAGGACGTTGCAGTAGCGGCAGCGCTCTAGGTAG AAGCCCGTGCCTCCTCCTCACGCTCCCCGCAGGGGACGTTGCAGTAGCGGCAGCGCTCTAGGTAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63696742..63697390 32194978 MeRIP-seq:(Medium) rs748292712 Functional Loss SNV dbSNP153 33..33 33 - - - 83639 RMVar_ID_83639 Human_SNP_ID_687105850 m1A Human chr20 + 63699878 63699878 63699878 GGCCCAGGCGTGGGGTATAGGTCTTCCCCCGCAGGCCTCAGCCCTGTCCCGAGGCTGCATCACAA GGCCCAGGCGTGGGGTATAGGTCTTCCCCCGCGGGCCTCAGCCCTGTCCCGAGGCTGCATCACAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63699831..63700070 26863196 MeRIP-seq:(Medium) rs1355908102 Functional Loss SNV dbSNP153 33..33 33 - - - 83640 RMVar_ID_83640 Human_SNP_ID_687105851 m1A Human chr20 + 63699878 63699878 63699878 GGCCCAGGCGTGGGGTATAGGTCTTCCCCCGCAGGCCTCAGCCCTGTCCCGAGGCTGCATCACAA GGCCCAGGCGTGGGGTATAGGTCTTCCCCCGCTGGCCTCAGCCCTGTCCCGAGGCTGCATCACAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63699831..63700070 26863196 MeRIP-seq:(Medium) rs1355908102 Functional Loss SNV dbSNP153 33..33 33 - - - 83641 RMVar_ID_83641 Human_SNP_ID_687106131 m1A Human chr20 + 63700486 63700486 63700486 CCCTCTGCCGCGGCGGCCGGTGCACATTCCGCACGACACACTTCACCATCCACTCGATGCCCTCG CCCTCTGCCGCGGCGGCCGGTGCACATTCCGCCCGACACACTTCACCATCCACTCGATGCCCTCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63700413..63700574 26863196 MeRIP-seq:(Medium) rs778964903 Functional Loss SNV dbSNP153 33..33 33 - - - 83642 RMVar_ID_83642 Human_SNP_ID_687106143 m1A Human chr20 + 63700498 63700498 63700498 GCGGCCGGTGCACATTCCGCACGACACACTTCACCATCCACTCGATGCCCTCGCGCACCCCTTTG GCGGCCGGTGCACATTCCGCACGACACACTTCCCCATCCACTCGATGCCCTCGCGCACCCCTTTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63699538..63700735 32194978 MeRIP-seq:(Medium) rs759983214 Functional Loss SNV dbSNP153 33..33 33 - - - 83643 RMVar_ID_83643 Human_SNP_ID_687106248 m1A Human chr20 - 63700681 63700681 63700681 ACCTCCCCCAGACGTGCCTCTCAATCCCTGACATCAAGACGGCCTTCAGCGACTGCACCAGCAAG ACCTCCCCCAGACGTGCCTCTCAATCCCTGACGTCAAGACGGCCTTCAGCGACTGCACCAGCAAG T C ARFRP1 Ensembl:ENSG00000101246 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63700559..63700725 26863196 MeRIP-seq:(Medium) rs1187518396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1600802,Human_RBP_ID_9389753,Human_RBP_ID_18495453,Human_RBP_ID_19004794,Human_RBP_ID_26343263,Human_RBP_ID_27299919 Human_Splice_Rec_2104748,Human_Splice_Rec_2104749,Human_Splice_Rec_2104762,Human_Splice_Rec_2104763,Human_Splice_Rec_2104774,Human_Splice_Rec_2104786,Human_Splice_Rec_2104787,Human_Splice_Rec_2104789,Human_Splice_Rec_2104792,Human_Splice_Rec_2104793,Human_Splice_Rec_2104806,Human_Splice_Rec_2104807,Human_Splice_Rec_2104820,Human_Splice_Rec_2104830,Human_Splice_Rec_2104831,Human_Splice_Rec_2104836,Human_Splice_Rec_2104848,Human_Splice_Rec_2104849 RMVar_hsa_circ_314627 83644 RMVar_ID_83644 Human_SNP_ID_687106714 m1A Human chr20 - 63701897 63701895 63701898 TGAGGCGCTGCCTCTCCTGCCCTCCCCAGAGAAGGTGGTGACCAGCGAGGCGCTGTGCGGTGTCC TGAGGCGCTGCCTCTCCTGCCCTCCCCAGAG___GTGGTGACCAGCGAGGCGCTGTGCGGTGTCC CCTT C ARFRP1 Ensembl:ENSG00000101246 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63701826..63701955 26863196 MeRIP-seq:(Medium) rs1313304125 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1068217,Human_RBP_ID_5385829,Human_RBP_ID_19006498 Human_Splice_Rec_2104746,Human_Splice_Rec_2104747,Human_Splice_Rec_2104760,Human_Splice_Rec_2104761,Human_Splice_Rec_2104784,Human_Splice_Rec_2104785,Human_Splice_Rec_2104804,Human_Splice_Rec_2104805,Human_Splice_Rec_2104818,Human_Splice_Rec_2104819,Human_Splice_Rec_2104834,Human_Splice_Rec_2104835,Human_Splice_Rec_2104846,Human_Splice_Rec_2104847,Human_Splice_Rec_2104856 RMVar_hsa_circ_314627 83645 RMVar_ID_83645 Human_SNP_ID_687106896 m1A Human chr20 - 63702148 63702138 63702149 ACTCCACCGACGAGGAGAGGCTGGCTGAGTCCAAGCAGGCGTTTGGTGAGTGCGGCCTGGCTGCT ACTCCACCGACGAGGAGAGGCTGGCTGAGTC___________TTGGTGAGTGCGGCCTGGCTGCT AACGCCTGCTTG A ARFRP1 Ensembl:ENSG00000101246 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63701296..63702438 32194978 MeRIP-seq:(Medium) rs1436984308 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_19006500,Human_RBP_ID_26343265 Human_Splice_Rec_2104744,Human_Splice_Rec_2104745,Human_Splice_Rec_2104758,Human_Splice_Rec_2104759,Human_Splice_Rec_2104772,Human_Splice_Rec_2104773,Human_Splice_Rec_2104782,Human_Splice_Rec_2104783,Human_Splice_Rec_2104802,Human_Splice_Rec_2104803,Human_Splice_Rec_2104816,Human_Splice_Rec_2104817,Human_Splice_Rec_2104828,Human_Splice_Rec_2104829,Human_Splice_Rec_2104833,Human_Splice_Rec_2104844,Human_Splice_Rec_2104845,Human_Splice_Rec_2104854,Human_Splice_Rec_2104855 RMVar_hsa_circ_314627 83646 RMVar_ID_83646 Human_SNP_ID_687106902 m1A Human chr20 - 63702148 63702148 63702148 ACTCCACCGACGAGGAGAGGCTGGCTGAGTCCAAGCAGGCGTTTGGTGAGTGCGGCCTGGCTGCT ACTCCACCGACGAGGAGAGGCTGGCTGAGTCCCAGCAGGCGTTTGGTGAGTGCGGCCTGGCTGCT T G ARFRP1 Ensembl:ENSG00000101246 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63701296..63702438 32194978 MeRIP-seq:(Medium) rs759998328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19006500,Human_RBP_ID_26343265 Human_Splice_Rec_2104744,Human_Splice_Rec_2104745,Human_Splice_Rec_2104758,Human_Splice_Rec_2104759,Human_Splice_Rec_2104772,Human_Splice_Rec_2104773,Human_Splice_Rec_2104782,Human_Splice_Rec_2104783,Human_Splice_Rec_2104802,Human_Splice_Rec_2104803,Human_Splice_Rec_2104816,Human_Splice_Rec_2104817,Human_Splice_Rec_2104828,Human_Splice_Rec_2104829,Human_Splice_Rec_2104833,Human_Splice_Rec_2104844,Human_Splice_Rec_2104845,Human_Splice_Rec_2104854,Human_Splice_Rec_2104855 RMVar_hsa_circ_314627 83647 RMVar_ID_83647 Human_SNP_ID_687107812 m1A Human chr20 - 63704963 63704951 63704963 GGCAGCAGGATCCACAGAGCTGTGGTTGGCCCAGCAGGGAGCCCTGGAGGAGAACTGGCTATGCT GGCAGCAGGATCCACAGAGCTGTGGTTGGCCC____________TGGAGGAGAACTGGCTATGCT AGGGCTCCCTGCT A ARFRP1 Ensembl:ENSG00000101246 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63704960..63705130 26863196 MeRIP-seq:(Medium) rs1213101333 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_264788,Human_RBP_ID_3654501,Human_RBP_ID_5384272,Human_RBP_ID_8113644,Human_RBP_ID_9431413,Human_RBP_ID_18423304,Human_RBP_ID_18495464,Human_RBP_ID_20681254,Human_RBP_ID_22601581,Human_RBP_ID_22722405,Human_RBP_ID_22743573,Human_RBP_ID_23005290 RMVar_hsa_circ_314627 83648 RMVar_ID_83648 Human_SNP_ID_687108253 m1A Human chr20 + 63706426 63706426 63706426 AAGTCCCAGAACATGAGCCGAGCCTTTCCCACATCCACAGTGCCGACTGGGGAGAGGAGGAAACA AAGTCCCAGAACATGAGCCGAGCCTTTCCCACGTCCACAGTGCCGACTGGGGAGAGGAGGAAACA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63706376..63706425 32194978 MeRIP-seq:(Medium) rs879127624 Functional Loss SNV dbSNP153 33..33 33 - - - 83649 RMVar_ID_83649 Human_SNP_ID_687113383 m1A Human chr20 - 63723021 63723021 63723021 AGGGAGGATGGAACTATGTCAGAGGAAAAGGGAGGTTGGGACTGTGCTATAGGAAAATGGAGGGG AGGGAGGATGGAACTATGTCAGAGGAAAAGGGCGGTTGGGACTGTGCTATAGGAAAATGGAGGGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63722995..63723252 26863196 MeRIP-seq:(Medium) rs991615295 Functional Loss SNV dbSNP153 33..33 33 - - - 83650 RMVar_ID_83650 Human_SNP_ID_687116463 m1A Human chr20 + 63732382 63732381 63732383 GTGTGTGCATGTGTCAGGGTGTGTGTGCGCGCATGTGTGTGGGTGAGGGCCTGTGTGTGCGTGTG GTGTGTGCATGTGTCAGGGTGTGTGTGCGCGC__GTGTGTGGGTGAGGGCCTGTGTGTGCGTGTG CAT C AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63732212..63732479 26863196 MeRIP-seq:(Medium) rs1309035488 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5296841,Human_RBP_ID_5652441,Human_RBP_ID_8204383,Human_RBP_ID_9354158,Human_RBP_ID_17282873,Human_RBP_ID_17670883,Human_RBP_ID_21983224,Human_RBP_ID_23115381,Human_RBP_ID_23916337,Human_RBP_ID_27840610 83651 RMVar_ID_83651 Human_SNP_ID_687117333 m1A Human chr20 + 63733672 63733672 63733672 GCCGTGGTGGAGGGGGACGGCATCCTGCCCCCACTGCGCACAGAGGCCACAGAGTCCGACTCAGA GCCGTGGTGGAGGGGGACGGCATCCTGCCCCCGCTGCGCACAGAGGCCACAGAGTCCGACTCAGA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63733585..63733674 26863196 MeRIP-seq:(Medium) rs374194625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18777196 Human_Splice_Rec_2104866,Human_Splice_Rec_2104867,Human_Splice_Rec_2104878,Human_Splice_Rec_2104879,Human_Splice_Rec_2104890,Human_Splice_Rec_2104900,Human_Splice_Rec_2104901,Human_Splice_Rec_2104914,Human_Splice_Rec_2104915,Human_Splice_Rec_2104926,Human_Splice_Rec_2104927,Human_Splice_Rec_2104936,Human_Splice_Rec_2104942,Human_Splice_Rec_2104943,Human_Splice_Rec_2104948,Human_Splice_Rec_2104954,Human_Splice_Rec_2104955,Human_Splice_Rec_2104972 RMVar_hsa_circ_3494,RMVar_hsa_circ_52097 83652 RMVar_ID_83652 Human_SNP_ID_687117342 m1A Human chr20 + 63733690 63733690 63733690 GGCATCCTGCCCCCACTGCGCACAGAGGCCACAGAGTCCGACTCAGACAGCGACGGTACGGGTGA GGCATCCTGCCCCCACTGCGCACAGAGGCCACGGAGTCCGACTCAGACAGCGACGGTACGGGTGA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63733641..63734529 26863196 MeRIP-seq:(Medium) rs751104448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18777196 Human_Splice_Rec_2104867,Human_Splice_Rec_2104879,Human_Splice_Rec_2104901,Human_Splice_Rec_2104915,Human_Splice_Rec_2104927,Human_Splice_Rec_2104937,Human_Splice_Rec_2104943,Human_Splice_Rec_2104955,Human_Splice_Rec_2104973 RMVar_hsa_circ_3494,RMVar_hsa_circ_52097 83653 RMVar_ID_83653 Human_SNP_ID_687118696 m1A Human chr20 + 63737437 63737437 63737437 CTGTGCTGAGTCAGAGCTGGAACGGGAGACGCAGGAGCCCCGCAGCCGCGGGAGGTGCAGATTTG CTGTGCTGAGTCAGAGCTGGAACGGGAGACGCGGGAGCCCCGCAGCCGCGGGAGGTGCAGATTTG A G AL121845.3,LIME1 Ensembl:ENSG00000273154,Ensembl:ENSG00000203896 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63737387..63737592 26863196 MeRIP-seq:(Medium) rs1318047769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22672870 RMVar_hsa_circ_18652 83654 RMVar_ID_83654 Human_SNP_ID_687119130 m1A Human chr20 + 63738255 63738255 63738255 GCTGGAGGTGTCCAGGGACATCACCGGACCGCAGGCAGCCCCCTCTGCCTTCCCACACCAGGAGC GCTGGAGGTGTCCAGGGACATCACCGGACCGCGGGCAGCCCCCTCTGCCTTCCCACACCAGGAGC A G AL121845.3,LIME1 Ensembl:ENSG00000273154,Ensembl:ENSG00000203896 Protein coding,Protein coding 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63738204..63738904 32194978 MeRIP-seq:(Medium) rs1055096436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778456,Human_RBP_ID_4660638,Human_RBP_ID_18422956 Human_Splice_Rec_2104968,Human_Splice_Rec_2104980,Human_Splice_Rec_2104986,Human_Splice_Rec_2104994,Human_Splice_Rec_2105010,Human_Splice_Rec_2105020,Human_Splice_Rec_2105030,Human_Splice_Rec_2105038,Human_Splice_Rec_2105048 Human_miRNA_ID_2274169,Human_miRNA_ID_2933162 RMVar_hsa_circ_211338,RMVar_hsa_circ_116229 83655 RMVar_ID_83655 Human_SNP_ID_687119337 m1A Human chr20 - 63738710 63738710 63738710 CCAGGGCCCTGAGCGGGAGGGTCTGGTAGGCCAGGTCACCCGCCAGGGCCAGAATCGCTCCCTGG CCAGGGCCCTGAGCGGGAGGGTCTGGTAGGCCCGGTCACCCGCCAGGGCCAGAATCGCTCCCTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63738661..63739042 26863196 MeRIP-seq:(Medium) rs140720564 Functional Loss SNV dbSNP153 33..33 33 - - - 83656 RMVar_ID_83656 Human_SNP_ID_687119644 m1A Human chr20 - 63739579 63739579 63739579 CCCCTCCGGGTCGCTCCCGCGCTGGCCTAGGGAGGGAGGCCCGGCCCGGCACAGCTCCGAGGCCT CCCCTCCGGGTCGCTCCCGCGCTGGCCTAGGGTGGGAGGCCCGGCCCGGCACAGCTCCGAGGCCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63739353..63739690 26863196 MeRIP-seq:(Medium) rs1167746642 Functional Loss SNV dbSNP153 33..33 33 - - - 83657 RMVar_ID_83657 Human_SNP_ID_687119825 m1A Human chr20 - 63739871 63739871 63739871 GCCGGGCGCCGAGGCTGCAGCGGCGAGGGCTGACTCTCAGGACGCGGCCCCGGGCCGGGCCGGGC GCCGGGCGCCGAGGCTGCAGCGGCGAGGGCTGTCTCTCAGGACGCGGCCCCGGGCCGGGCCGGGC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:63739801..63739925 26863410 MeRIP-seq:(Medium) rs1568810785 Functional Loss SNV dbSNP153 33..33 33 - - - 83658 RMVar_ID_83658 Human_SNP_ID_687119865 m1A Human chr20 - 63739976 63739976 63739976 GGCGCGCGGCCCCGGACCCTCCGCGCGCAGCCACGGCGCCTCGGCCCGCAGCGCACTGGGGTCCC GGCGCGCGGCCCCGGACCCTCCGCGCGCAGCCTCGGCGCCTCGGCCCGCAGCGCACTGGGGTCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:63739776..63740091;chr20:63739810..63740092 26863196 MeRIP-seq:(Medium) rs1015743280 Functional Loss SNV dbSNP153 33..33 33 - - - 83659 RMVar_ID_83659 Human_SNP_ID_687120364 m1A Human chr20 - 63741393 63741393 63741393 TTGTAAGGGCAGCGGCAGCCATGACCTCGTCCAGCCGGGCTTTTCCTGGGGTGGCTCTGGAGGAG TTGTAAGGGCAGCGGCAGCCATGACCTCGTCCGGCCGGGCTTTTCCTGGGGTGGCTCTGGAGGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63738854..63741489 26863196 MeRIP-seq:(Medium) rs1333383475 Functional Loss SNV dbSNP153 33..33 33 - - - 83660 RMVar_ID_83660 Human_SNP_ID_687120848 m1A Human chr20 + 63742374 63742374 63742374 GGCAGAGCCTGAGCAGAGTGATGGTGAGGAGGACTTCTACTACACAGAGCTGGATGTTGGTGTGG GGCAGAGCCTGAGCAGAGTGATGGTGAGGAGGGCTTCTACTACACAGAGCTGGATGTTGGTGTGG A G SLC2A4RG Ensembl:ENSG00000125520 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63742047..63743150 26863196 MeRIP-seq:(Medium) rs889133526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568798,Human_RBP_ID_924242,Human_RBP_ID_1600833,Human_RBP_ID_1932955,Human_RBP_ID_3653403,Human_RBP_ID_8538539,Human_RBP_ID_14168329,Human_RBP_ID_18777237,Human_RBP_ID_26821131 Human_Splice_Rec_2105066,Human_Splice_Rec_2105082,Human_Splice_Rec_2105086,Human_Splice_Rec_2105094,Human_Splice_Rec_2105098 83661 RMVar_ID_83661 Human_SNP_ID_687120916 m1A Human chr20 + 63742510 63742510 63742510 CGCCTGGAGCTGCCAGAGCTGCTGGAGCCCCCAGCCCTGCCTAGTCCCCTGCGGCCGCCTGCCCC CGCCTGGAGCTGCCAGAGCTGCTGGAGCCCCCGGCCCTGCCTAGTCCCCTGCGGCCGCCTGCCCC A G SLC2A4RG Ensembl:ENSG00000125520 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:63742376..63742669 26863410 MeRIP-seq:(Medium) rs1166921914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568802,Human_RBP_ID_5132708,Human_RBP_ID_5200554,Human_RBP_ID_5385871 83662 RMVar_ID_83662 Human_SNP_ID_687120945 m1A Human chr20 - 63742548 63742548 63742548 TAGCAACGGTGCTCAGGACAGGGGGCGGGGGCAGGGGCGGGGCAGGCGGCCGCAGGGGACTAGGC TAGCAACGGTGCTCAGGACAGGGGGCGGGGGCGGGGGCGGGGCAGGCGGCCGCAGGGGACTAGGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr20:63742458..63742547;chr20:63742468..63742555 26863410 MeRIP-seq:(Medium) rs749550960 Functional Loss SNV dbSNP153 33..33 33 - - - 83663 RMVar_ID_83663 Human_SNP_ID_687122542 m1A Human chr20 - 63746850 63746850 63746850 GTGTGTGTCCGGTGGGTCTCCACTGCGGGGCCAGGGCCACGCTCACCCCTCTCGCGGCCCCTCCT GTGTGTGTCCGGTGGGTCTCCACTGCGGGGCCCGGGCCACGCTCACCCCTCTCGCGGCCCCTCCT T G ZBTB46 Ensembl:ENSG00000130584 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63746842..63747197 26863196 MeRIP-seq:(Medium) rs531188495 Functional Loss SNV dbSNP153 33..33 33 - - - 83664 RMVar_ID_83664 Human_SNP_ID_687126354 m1A Human chr20 - 63758147 63758147 63758147 GAGCTCTGGACGGGGCGGGTGGAGGGAGTGTGAGCTCTGGATGGGGCGGGTGGAGGGAGTGTGAG GAGCTCTGGACGGGGCGGGTGGAGGGAGTGTGCGCTCTGGATGGGGCGGGTGGAGGGAGTGTGAG T G ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63758138..63758508 26863196 MeRIP-seq:(Medium) rs190753955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83651,RMVar_hsa_circ_211341,RMVar_hsa_circ_269700,RMVar_hsa_circ_211340,RMVar_hsa_circ_344970 83665 RMVar_ID_83665 Human_SNP_ID_687126391 m1A Human chr20 - 63758245 63758245 63758245 CAGGGGTGATTAGGGGAGGGGATACTGGCTGTAGTGTGAGAACCTATGGAGCAGGAGGAGGGAGT CAGGGGTGATTAGGGGAGGGGATACTGGCTGTGGTGTGAGAACCTATGGAGCAGGAGGAGGGAGT T C ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63758238..63758420 26863196 MeRIP-seq:(Medium) rs1343976255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83651,RMVar_hsa_circ_211341,RMVar_hsa_circ_269700,RMVar_hsa_circ_211340,RMVar_hsa_circ_344970 83666 RMVar_ID_83666 Human_SNP_ID_687149460 m1A Human chr20 - 63831158 63831128 63831158 CCGGACGCAGCGCCCTCCCGGCGGCGGCGGCGATCACCGGCGCCGGCCCGGCGGCCGCGGCGCCC CCGGACGCAGCGCCCTCCCGGCGGCGGCGGCG______________________________CCC GCGCCGCGGCCGCCGGGCCGGCGCCGGTGAT G ZBTB46 Ensembl:ENSG00000130584 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63831123..63831263 26863196 MeRIP-seq:(Medium) rs1257597366 Functional Loss DEL dbSNP153 33..62 33 - - - Human_RBP_ID_4657814 Human_Splice_Rec_2105107,Human_Splice_Rec_2105121 83667 RMVar_ID_83667 Human_SNP_ID_687149462 m1A Human chr20 - 63831158 63831135 63831159 CCGGACGCAGCGCCCTCCCGGCGGCGGCGGCGATCACCGGCGCCGGCCCGGCGGCCGCGGCGCCC CCGGACGCAGCGCCCTCCCGGCGGCGGCGGC________________________CGCGGCGCCC GGCCGCCGGGCCGGCGCCGGTGATC G ZBTB46 Ensembl:ENSG00000130584 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63831123..63831263 26863196 MeRIP-seq:(Medium) rs1480075291 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_4657814 Human_Splice_Rec_2105107,Human_Splice_Rec_2105121 83668 RMVar_ID_83668 Human_SNP_ID_687151085 m1A Human chr20 - 63835761 63835760 63835761 CGGCAGGTGTGGCCTGGCCTCTGTCCCAGGGAAGGTCTGGAATGCAGATCCCTGGTGTGGTGGCC CGGCAGGTGTGGCCTGGCCTCTGTCCCAGGGA_GGTCTGGAATGCAGATCCCTGGTGTGGTGGCC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63835759..63835872 26863196 MeRIP-seq:(Medium) rs1466996615 Functional Loss DEL dbSNP153 33..33 33 - - - 83669 RMVar_ID_83669 Human_SNP_ID_687154378 m1A Human chr20 + 63847144 63847137 63847145 GCAGAGACACACACACAGACACTGACACACACAGACACACAGACACTGACACACACACATGCAGA GCAGAGACACACACACAGACACTGAC________ACACACAGACACTGACACACACACATGCAGA CACACACAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63846909..63847300 26863196 MeRIP-seq:(Medium) rs1328992010 Functional Loss DEL dbSNP153 27..34 33 - - - 83670 RMVar_ID_83670 Human_SNP_ID_687154380 m1A Human chr20 + 63847144 63847141 63847145 GCAGAGACACACACACAGACACTGACACACACAGACACACAGACACTGACACACACACATGCAGA GCAGAGACACACACACAGACACTGACACAC____ACACACAGACACTGACACACACACATGCAGA CACAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63846909..63847300 26863196 MeRIP-seq:(Medium) rs1259340749 Functional Loss DEL dbSNP153 31..34 33 - - - 83671 RMVar_ID_83671 Human_SNP_ID_687155826 m1A Human chr20 - 63851077 63851077 63851077 GCAGTTGCACCACAGAGGGGGAAACTGCAAGTAGTCATTTCAGAGTGCGTGGGTTTTGGTGACAG GCAGTTGCACCACAGAGGGGGAAACTGCAAGTCGTCATTTCAGAGTGCGTGGGTTTTGGTGACAG T G HSALNG0131698 RNACentral:URS0000EBB54B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63851028..63851223 26863196 MeRIP-seq:(Medium) rs994444552 Functional Loss SNV dbSNP153 33..33 33 - - - 83672 RMVar_ID_83672 Human_SNP_ID_687156589 m1A Human chr20 - 63853799 63853799 63853799 CAGGAGGGTGAGGTTGGATGACCTGAGTGGAGACAGGGACCAGGAGGGTGAGGGTGGATGACCTG CAGGAGGGTGAGGTTGGATGACCTGAGTGGAGGCAGGGACCAGGAGGGTGAGGGTGGATGACCTG T C HSALNG0131698 RNACentral:URS0000EBB54B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63853797..63853896 26863196 MeRIP-seq:(Medium) rs1341843098 Functional Loss SNV dbSNP153 33..33 33 - - - 83673 RMVar_ID_83673 Human_SNP_ID_687159783 m1A Human chr20 + 63863020 63863020 63863020 CTGGCCTTCTTGGTTCACCTCCCCATACCGCCAACCATTGCAGGGGGCCGGCGCCGACGCGGGGC CTGGCCTTCTTGGTTCACCTCCCCATACCGCCCACCATTGCAGGGGGCCGGCGCCGACGCGGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63862982..63863269 26863196 MeRIP-seq:(Medium) rs1350963598 Functional Loss SNV dbSNP153 33..33 33 - - - 83674 RMVar_ID_83674 Human_SNP_ID_687159866 m1A Human chr20 - 63863162 63863162 63863162 AGAAAGGAGGGGACAGAGCTAGGAAGAATGGGAGGACGGTCAGAACGCCCCTGTGAAGGAAGGAG AGAAAGGAGGGGACAGAGCTAGGAAGAATGGGCGGACGGTCAGAACGCCCCTGTGAAGGAAGGAG T G AL118506.1 Ensembl:ENSG00000268858 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63863122..63863208 26863196 MeRIP-seq:(Medium) rs1232340042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264792,Human_RBP_ID_4657831,Human_RBP_ID_5596338,Human_RBP_ID_18471285,Human_RBP_ID_22361633,Human_RBP_ID_22722783,Human_RBP_ID_24553527,Human_RBP_ID_27573422 83675 RMVar_ID_83675 Human_SNP_ID_687160107 m1A Human chr20 - 63864267 63864267 63864267 ACCAGCGCTGCGCCCTCCCCACTCCACAGATGAGGAAGCTGAGGTTAAAGTCACTTGCCCCAGGT ACCAGCGCTGCGCCCTCCCCACTCCACAGATGGGGAAGCTGAGGTTAAAGTCACTTGCCCCAGGT T C AL118506.1 Ensembl:ENSG00000268858 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63864192..63864324 32194978 MeRIP-seq:(Medium) rs575940129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27024780 Human_miRNA_ID_3202675,Human_miRNA_ID_3208922,Human_miRNA_ID_3210979 83676 RMVar_ID_83676 Human_SNP_ID_687160506 m1A Human chr20 - 63865372 63865372 63865372 GGGCCGGGCCCGGCAGGTACCTTGGCCGGCGGAGTCCATGTTCGGGCGGCGTCCGGACCGCTGTC GGGCCGGGCCCGGCAGGTACCTTGGCCGGCGGGGTCCATGTTCGGGCGGCGTCCGGACCGCTGTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr20:63865276..63865400;chr20:63865327..63873714 26863410,32194978 MeRIP-seq:(Medium) rs1468829200 Functional Loss SNV dbSNP153 33..33 33 - - - 83677 RMVar_ID_83677 Human_SNP_ID_687160507 m1A Human chr20 - 63865372 63865372 63865372 GGGCCGGGCCCGGCAGGTACCTTGGCCGGCGGAGTCCATGTTCGGGCGGCGTCCGGACCGCTGTC GGGCCGGGCCCGGCAGGTACCTTGGCCGGCGGCGTCCATGTTCGGGCGGCGTCCGGACCGCTGTC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr20:63865276..63865400;chr20:63865327..63873714 26863410,32194978 MeRIP-seq:(Medium) rs1468829200 Functional Loss SNV dbSNP153 33..33 33 - - - 83678 RMVar_ID_83678 Human_SNP_ID_687163971 m1A Human chr20 - 63875803 63875803 63875803 TCTCAGAAGTTTTCACATAGCTAAAAACAGAAAGTCTACAGTGAATTATTTAGAAGAACAATTTT TCTCAGAAGTTTTCACATAGCTAAAAACAGAAGGTCTACAGTGAATTATTTAGAAGAACAATTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63875801..63875825 26863196 MeRIP-seq:(Medium) rs201180118 Functional Loss SNV dbSNP153 33..33 33 - - - 83679 RMVar_ID_83679 Human_SNP_ID_687164694 m1A Human chr20 + 63877945 63877945 63877945 GGTTTCTGGTGGGAAGGCCCAGGCCGAGGGCGATGGTTTCTGCCGGGACGGCCGAGGCCGAGGGC GGTTTCTGGTGGGAAGGCCCAGGCCGAGGGCGGTGGTTTCTGCCGGGACGGCCGAGGCCGAGGGC A G TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63877930..63878155 26863196 MeRIP-seq:(Medium) rs1341159804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8204404,Human_RBP_ID_17143379,Human_RBP_ID_23119745 RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 83680 RMVar_ID_83680 Human_SNP_ID_687165820 m1A Human chr20 + 63882380 63882380 63882380 GCGTGTTCTCTGTAGTCAGAGGGGCTGTGAGAAGACAGGAAAGCGAGCTTAGTGGGTATCAGGCA GCGTGTTCTCTGTAGTCAGAGGGGCTGTGAGAGGACAGGAAAGCGAGCTTAGTGGGTATCAGGCA A G TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63882378..63882464 26863196 MeRIP-seq:(Medium) rs1255091525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5323425,Human_RBP_ID_14168843 RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 83681 RMVar_ID_83681 Human_SNP_ID_687165916 m1A Human chr20 - 63882687 63882687 63882687 GCTGGAAGACACACCAGTTAAATCAACCAGACAGCATGGGCGGGTCACCACCCACAGCCAAGCAA GCTGGAAGACACACCAGTTAAATCAACCAGACGGCATGGGCGGGTCACCACCCACAGCCAAGCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63882685..63882794 26863196 MeRIP-seq:(Medium) rs1229786909 Functional Loss SNV dbSNP153 33..33 33 - - - 83682 RMVar_ID_83682 Human_SNP_ID_687168684 m1A Human chr20 + 63891371 63891371 63891371 CCCTTGGGGATGGCACTCCACACACGACAGAGATGCAGGGGCCAGGGAAGCCCAGCGCTCGGTGC CCCTTGGGGATGGCACTCCACACACGACAGAGGTGCAGGGGCCAGGGAAGCCCAGCGCTCGGTGC A G TPD52L2 Ensembl:ENSG00000101150 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63891321..63891492 26863196 MeRIP-seq:(Medium) rs1405415423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568894,Human_RBP_ID_8205272,Human_RBP_ID_26493768 83683 RMVar_ID_83683 Human_SNP_ID_687169803 m1A Human chr20 - 63895176 63895176 63895176 GCGGCGGCGGCGGCAGAGGGCGCGGGTGCGGCACCGGCAGCGGCAGCGGCAGCGGCAGCGGAGAC GCGGCGGCGGCGGCAGAGGGCGCGGGTGCGGCTCCGGCAGCGGCAGCGGCAGCGGCAGCGGAGAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63895139..63895272 26863196 MeRIP-seq:(Medium) rs1043057997 Functional Loss SNV dbSNP153 33..33 33 - - - 83684 RMVar_ID_83684 Human_SNP_ID_687169809 m1A Human chr20 + 63895182 63895182 63895182 GCTGCCGCTGCCGCTGCCGCTGCCGGTGCCGCACCCGCGCCCTCTGCCGCCGCCGCCGCCGCCGC GCTGCCGCTGCCGCTGCCGCTGCCGGTGCCGCGCCCGCGCCCTCTGCCGCCGCCGCCGCCGCCGC A G DNAJC5 Ensembl:ENSG00000101152 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr20:63895180..63895314;chr20:63895143..63895271 26863196 MeRIP-seq:(Medium) rs1347975109 Functional Loss SNV dbSNP153 33..33 33 - - - 83685 RMVar_ID_83685 Human_SNP_ID_687169844 m1A Human chr20 + 63895226 63895226 63895226 TGCCGCCGCCGCCGCCGCCGCCCGGGGTCTCCAGGCTGAGGAGTGCGTCGGCCGCTGCCCAGCAG TGCCGCCGCCGCCGCCGCCGCCCGGGGTCTCCGGGCTGAGGAGTGCGTCGGCCGCTGCCCAGCAG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:63895217..63895661 26863196 MeRIP-seq:(Medium) rs750302498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659570,Human_RBP_ID_5385888,Human_RBP_ID_9331717,Human_RBP_ID_22723039,Human_RBP_ID_23258252,Human_RBP_ID_24424704,Human_RBP_ID_26788733 Human_Splice_Rec_2105263,Human_Splice_Rec_2105271 Clinvar_Rec_434 83686 RMVar_ID_83686 Human_SNP_ID_687169924 m1A Human chr20 + 63895437 63895437 63895437 GGGGCGGCACTCCAGAGCCGGAAATGGCGGCGACCCCCGGGCCGGGGCTGCGCGGGCGCTCGGGG GGGGCGGCACTCCAGAGCCGGAAATGGCGGCGGCCCCCGGGCCGGGGCTGCGCGGGCGCTCGGGG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63895435..63895546 26863196 MeRIP-seq:(Medium) rs1405118684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264796,Human_RBP_ID_3654527,Human_RBP_ID_5240337,Human_RBP_ID_5323091,Human_RBP_ID_5384306,Human_RBP_ID_8204409,Human_RBP_ID_8729064,Human_RBP_ID_9331718,Human_RBP_ID_9430937,Human_RBP_ID_18423259,Human_RBP_ID_18463560,Human_RBP_ID_18951006,Human_RBP_ID_22361635,Human_RBP_ID_22549600,Human_RBP_ID_22700956,Human_RBP_ID_22722275,Human_RBP_ID_22743771,Human_RBP_ID_26788736 83687 RMVar_ID_83687 Human_SNP_ID_687175833 m1A Human chr20 - 63915119 63915116 63915119 GATACGGACCAGCTCCTATCTGCCTGAGGCCCACCCAGTGCCCCAGGTCCCAGGAGCATCCATGG GATACGGACCAGCTCCTATCTGCCTGAGGCCC___CAGTGCCCCAGGTCCCAGGAGCATCCATGG GGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:63915114..63915240 26863196 MeRIP-seq:(Medium) rs1186820529 Functional Loss DEL dbSNP153 33..35 33 - - - 83688 RMVar_ID_83688 Human_SNP_ID_687179460 m1A Human chr20 - 63926607 63926607 63926607 CTGTTATTATCCCACTGCTTTCCTCAATCTTCAGCAAATGGCAGAGCATGAGATTCCGTCTCCAT CTGTTATTATCCCACTGCTTTCCTCAATCTTCGGCAAATGGCAGAGCATGAGATTCCGTCTCCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63926605..63926699 26863196 MeRIP-seq:(Medium) rs1438768365 Functional Loss SNV dbSNP153 33..33 33 - - - 83689 RMVar_ID_83689 Human_SNP_ID_687181600 m1A Human chr20 + 63933267 63933267 63933267 TTGCCCTCAGCAGCCACCCGAGGCTGTGCAGAAGGGTAGGTTCAGGTTGACCAGGAAGCTGCCAA TTGCCCTCAGCAGCCACCCGAGGCTGTGCAGATGGGTAGGTTCAGGTTGACCAGGAAGCTGCCAA A T DNAJC5 Ensembl:ENSG00000101152 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63933219..63933291 26863196 MeRIP-seq:(Medium) rs538696522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568924,Human_RBP_ID_7020514,Human_RBP_ID_14170390 RMVar_hsa_circ_76610,RMVar_hsa_circ_79675,RMVar_hsa_circ_211352,RMVar_hsa_circ_211353 83690 RMVar_ID_83690 Human_SNP_ID_687183900 m1A Human chr20 - 63940201 63940199 63940202 CCTATGCATTTCCGCGAGTGAGAATCATCACCACGGCGGTGGACAAGCGGGTCAATGACCTTTTC CCTATGCATTTCCGCGAGTGAGAATCATCAC___GGCGGTGGACAAGCGGGTCAATGACCTTTTC CGTG C UCKL1 Ensembl:ENSG00000198276 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63940176..63940200 32194978 MeRIP-seq:(Medium) rs1183971513 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9119125 Human_Splice_Rec_2105307,Human_Splice_Rec_2105331,Human_Splice_Rec_2105359 83691 RMVar_ID_83691 Human_SNP_ID_687184548 m1A Human chr20 + 63941550 63941550 63941550 GGGCCGGGCACAGGGCGGGCTCACACGTGCTGATAGGTGTCATACCCCAGAATGGGTAGCTTGTC GGGCCGGGCACAGGGCGGGCTCACACGTGCTGGTAGGTGTCATACCCCAGAATGGGTAGCTTGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63941501..63941594 26863196 MeRIP-seq:(Medium) rs1163186114 Functional Loss SNV dbSNP153 33..33 33 - - - 83692 RMVar_ID_83692 Human_SNP_ID_687184617 m1A Human chr20 - 63941711 63941711 63941711 ATCCCCAGGCTTGGGCAGCGGGGCGGGACGGGACAGCCAAGAGACACTGAGCCAGCTTTGCCCCC ATCCCCAGGCTTGGGCAGCGGGGCGGGACGGGGCAGCCAAGAGACACTGAGCCAGCTTTGCCCCC T C UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs817370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132313,Human_RBP_ID_17571998 GWAS_ID_10096 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83693 RMVar_ID_83693 Human_SNP_ID_687184730 m1A Human chr20 + 63941957 63941957 63941957 GTGGCAGGGGAAGGAAAGAGGCAGGGCACGGAATTGGGTGTGGCAGGGCAGAAAAGAGGCGTGAC GTGGCAGGGGAAGGAAAGAGGCAGGGCACGGAGTTGGGTGTGGCAGGGCAGAAAAGAGGCGTGAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63941758..63941989 26863196 MeRIP-seq:(Medium) rs960546180 Functional Loss SNV dbSNP153 33..33 33 - - - 83694 RMVar_ID_83694 Human_SNP_ID_687184731 m1A Human chr20 - 63941959 63941959 63941959 CTGTCACGCCTCTTTTCTGCCCTGCCACACCCAATTCCGTGCCCTGCCTCTTTCCTTCCCCTGCC CTGTCACGCCTCTTTTCTGCCCTGCCACACCCCATTCCGTGCCCTGCCTCTTTCCTTCCCCTGCC T G UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:63941585..63942025;chr20:63941768..63942000;chr20:63941780..63941994 26863196 MeRIP-seq:(Medium) rs544718357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132319,Human_RBP_ID_5323435,Human_RBP_ID_17086237,Human_RBP_ID_17659504,Human_RBP_ID_18951017,Human_RBP_ID_20680586,Human_RBP_ID_21983259,Human_RBP_ID_22507083,Human_RBP_ID_25631892 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83695 RMVar_ID_83695 Human_SNP_ID_687184824 m1A Human chr20 + 63942321 63942321 63942321 CGTGACAGCGGCAGGGAAAGGGGCGGGGCCGGAAATGGGGTGTGGCAGGGCAGAAAAGAGGCGTG CGTGACAGCGGCAGGGAAAGGGGCGGGGCCGGGAATGGGGTGTGGCAGGGCAGAAAAGAGGCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:63942276..63942649;chr20:63942276..63942626;chr20:63942276..63942489;chr20:63942271..63942456 26863196 MeRIP-seq:(Medium) rs2427570 Functional Loss SNV dbSNP153 33..33 33 - - - 83696 RMVar_ID_83696 Human_SNP_ID_687184827 m1A Human chr20 - 63942324 63942324 63942324 TGTCACGCCTCTTTTCTGCCCTGCCACACCCCATTTCCGGCCCCGCCCCTTTCCCTGCCGCTGTC TGTCACGCCTCTTTTCTGCCCTGCCACACCCCTTTTCCGGCCCCGCCCCTTTCCCTGCCGCTGTC T A UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63942228..63942433 26863196 MeRIP-seq:(Medium) rs1464200645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132320,Human_RBP_ID_17086238,Human_RBP_ID_18951018,Human_RBP_ID_27840628 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83697 RMVar_ID_83697 Human_SNP_ID_687184828 m1A Human chr20 - 63942324 63942324 63942324 TGTCACGCCTCTTTTCTGCCCTGCCACACCCCATTTCCGGCCCCGCCCCTTTCCCTGCCGCTGTC TGTCACGCCTCTTTTCTGCCCTGCCACACCCCCTTTCCGGCCCCGCCCCTTTCCCTGCCGCTGTC T G UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:63942228..63942433 26863196 MeRIP-seq:(Medium) rs1464200645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132320,Human_RBP_ID_17086238,Human_RBP_ID_18951018,Human_RBP_ID_27840628 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83698 RMVar_ID_83698 Human_SNP_ID_687184829 m1A Human chr20 - 63942329 63942328 63942329 GCCGCTGTCACGCCTCTTTTCTGCCCTGCCACACCCCATTTCCGGCCCCGCCCCTTTCCCTGCCG GCCGCTGTCACGCCTCTTTTCTGCCCTGCCAC_CCCCATTTCCGGCCCCGCCCCTTTCCCTGCCG GT G UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63942217..63942431 26863196 MeRIP-seq:(Medium) rs1330068653 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5132320,Human_RBP_ID_17086238,Human_RBP_ID_18951018,Human_RBP_ID_27840628 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83699 RMVar_ID_83699 Human_SNP_ID_687184830 m1A Human chr20 - 63942329 63942329 63942329 GCCGCTGTCACGCCTCTTTTCTGCCCTGCCACACCCCATTTCCGGCCCCGCCCCTTTCCCTGCCG GCCGCTGTCACGCCTCTTTTCTGCCCTGCCACCCCCCATTTCCGGCCCCGCCCCTTTCCCTGCCG T G UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:63942217..63942431 26863196 MeRIP-seq:(Medium) rs1379339773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132320,Human_RBP_ID_17086238,Human_RBP_ID_18951018,Human_RBP_ID_27840628 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 83700 RMVar_ID_83700 Human_SNP_ID_687185282 m1A Human chr20 + 63943667 63943667 63943667 CAGCTGTGCAAGTCTTACCTGACGCTGAGTTCACGCTGTGGCAGCAACACAGGAAGACACAAGGG CAGCTGTGCAAGTCTTACCTGACGCTGAGTTCTCGCTGTGGCAGCAACACAGGAAGACACAAGGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63943627..63943778 26863196 MeRIP-seq:(Medium) rs772335925 Functional Loss SNV dbSNP153 33..33 33 - - - 83701 RMVar_ID_83701 Human_SNP_ID_687185661 m1A Human chr20 - 63944684 63944684 63944684 TTTGTGGACACAGACTCCGACATCCGCCTGGTACGGCGGCTGCGCCGGGACATCAGTGAGCGCGG TTTGTGGACACAGACTCCGACATCCGCCTGGTCCGGCGGCTGCGCCGGGACATCAGTGAGCGCGG T G UCKL1 Ensembl:ENSG00000198276 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63944551..63944750 26863196 MeRIP-seq:(Medium) rs749443798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63258,Human_RBP_ID_568980,Human_RBP_ID_926767,Human_RBP_ID_3961112,Human_RBP_ID_9389784,Human_RBP_ID_18412967,Human_RBP_ID_18471227,Human_RBP_ID_22261074,Human_RBP_ID_23004914,Human_RBP_ID_26342580,Human_RBP_ID_27024943,Human_RBP_ID_27820003 Human_Splice_Rec_2105290,Human_Splice_Rec_2105318,Human_Splice_Rec_2105342,Human_Splice_Rec_2105368 Human_miRNA_ID_3011091,Human_miRNA_ID_3011092 RMVar_hsa_circ_35993,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_106331,RMVar_hsa_circ_122248,RMVar_hsa_circ_90432,RMVar_hsa_circ_211359,RMVar_hsa_circ_211360,RMVar_hsa_circ_211361 83702 RMVar_ID_83702 Human_SNP_ID_687185985 m1A Human chr20 + 63945617 63945616 63945617 CACCTCATGGACAGGGCGGCCAGGGCTGAGATACCAGCGGGGTGGGTATTCCCGGCGGGTGCTTA CACCTCATGGACAGGGCGGCCAGGGCTGAGAT_CCAGCGGGGTGGGTATTCCCGGCGGGTGCTTA TA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63945615..63946016 26863196 MeRIP-seq:(Medium) rs1236594458 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14170657 83703 RMVar_ID_83703 Human_SNP_ID_687185986 m1A Human chr20 + 63945617 63945617 63945617 CACCTCATGGACAGGGCGGCCAGGGCTGAGATACCAGCGGGGTGGGTATTCCCGGCGGGTGCTTA CACCTCATGGACAGGGCGGCCAGGGCTGAGATGCCAGCGGGGTGGGTATTCCCGGCGGGTGCTTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63945615..63946016 26863196 MeRIP-seq:(Medium) rs769154414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14170657 83704 RMVar_ID_83704 Human_SNP_ID_687186274 m1A Human chr20 - 63946223 63946223 63946223 GCAGTGCCTCTGGGAAGACCACTGTGGCCAGAATGATCATCGAGGCCCTGGATGTGCCCTGGGTG GCAGTGCCTCTGGGAAGACCACTGTGGCCAGAGTGATCATCGAGGCCCTGGATGTGCCCTGGGTG T C UCKL1 Ensembl:ENSG00000198276 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63945989..63946473 32194978 MeRIP-seq:(Medium) rs896195670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63262,Human_RBP_ID_8538704,Human_RBP_ID_27820511 Human_Splice_Rec_2105284,Human_Splice_Rec_2105285,Human_Splice_Rec_2105312,Human_Splice_Rec_2105313,Human_Splice_Rec_2105336,Human_Splice_Rec_2105337,Human_Splice_Rec_2105362,Human_Splice_Rec_2105363,Human_Splice_Rec_2105396 RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_106331,RMVar_hsa_circ_122248,RMVar_hsa_circ_105055,RMVar_hsa_circ_211359,RMVar_hsa_circ_211360,RMVar_hsa_circ_112425,RMVar_hsa_circ_302175,RMVar_hsa_circ_344523,RMVar_hsa_circ_211362,RMVar_hsa_circ_211363 83705 RMVar_ID_83705 Human_SNP_ID_687187327 m1A Human chr20 + 63948568 63948566 63948568 TGCGCCTCGGTGTGAGGAGGGAGGCGTGTGTGAGAGGGAGGGGATGTGTGTGAGAGGGAGGGGGC TGCGCCTCGGTGTGAGGAGGGAGGCGTGTGT__GAGGGAGGGGATGTGTGTGAGAGGGAGGGGGC TGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63948565..63948694 26863196 MeRIP-seq:(Medium) rs200573159 Functional Loss DEL dbSNP153 32..33 33 - - - 83706 RMVar_ID_83706 Human_SNP_ID_687187330 m1A Human chr20 + 63948568 63948568 63948568 TGCGCCTCGGTGTGAGGAGGGAGGCGTGTGTGAGAGGGAGGGGATGTGTGTGAGAGGGAGGGGGC TGCGCCTCGGTGTGAGGAGGGAGGCGTGTGTGTGAGGGAGGGGATGTGTGTGAGAGGGAGGGGGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63948565..63948694 26863196 MeRIP-seq:(Medium) rs6062596 Functional Loss SNV dbSNP153 33..33 33 - - - 83707 RMVar_ID_83707 Human_SNP_ID_687187432 m1A Human chr20 - 63948641 63948632 63948641 CTCCCTCTCACACACGCCCCTCCCTCTCACACACGCCCCTTCCCTCTCACACACGCCCCTCCCTC CTCCCTCTCACACACGCCCCTCCCTCTCACAC_________CCCTCTCACACACGCCCCTCCCTC GAAGGGGCGT G UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63948514..63948734 26863196 MeRIP-seq:(Medium) rs1569123506 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_206510,Human_RBP_ID_244626,Human_RBP_ID_264800,Human_RBP_ID_5132335,Human_RBP_ID_17086246,Human_RBP_ID_18951026,Human_RBP_ID_24553537,Human_RBP_ID_26761502,Human_RBP_ID_26788747,Human_RBP_ID_27840635 RMVar_hsa_circ_122248,RMVar_hsa_circ_211359,RMVar_hsa_circ_112425,RMVar_hsa_circ_211362 83708 RMVar_ID_83708 Human_SNP_ID_687189107 m1A Human chr20 + 63954224 63954224 63954224 CTTCCCTCAGCAGGACCTGCCCTGCACAGATCATGGGCAGCCTCCCTCTGCTCCCCACTTCCACA CTTCCCTCAGCAGGACCTGCCCTGCACAGATCGTGGGCAGCCTCCCTCTGCTCCCCACTTCCACA A G UCKL1-AS1 Ensembl:ENSG00000280213 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63954222..63954371 26863196 MeRIP-seq:(Medium) rs1477881616 Functional Loss SNV dbSNP153 33..33 33 - - - 83709 RMVar_ID_83709 Human_SNP_ID_687190387 m1A Human chr20 - 63957939 63957939 63957939 GCGTGACCCAGCGTCAGAGGGTCGGGGGAGGCATTCCTTCCTGTGTCCCAGAGCTTCACTGGTGG GCGTGACCCAGCGTCAGAGGGTCGGGGGAGGCGTTCCTTCCTGTGTCCCAGAGCTTCACTGGTGG T C ZNF512B Ensembl:ENSG00000196700 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:63957891..63958020;chr20:63957888..63958045 26863196 MeRIP-seq:(Medium) rs1214771156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3655485,Human_RBP_ID_17976630,Human_RBP_ID_27488668 Human_miRNA_ID_31392,Human_miRNA_ID_553236,Human_miRNA_ID_1068492,Human_miRNA_ID_1698197 83710 RMVar_ID_83710 Human_SNP_ID_687190396 m1A Human chr20 + 63957950 63957950 63957950 GCTCTGGGACACAGGAAGGAATGCCTCCCCCGACCCTCTGACGCTGGGTCACGCCCATCTCTGCC GCTCTGGGACACAGGAAGGAATGCCTCCCCCGGCCCTCTGACGCTGGGTCACGCCCATCTCTGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:63957899..63958099;chr20:63957899..63958014 26863196 MeRIP-seq:(Medium) rs988945816 Functional Loss SNV dbSNP153 33..33 33 - - - 83711 RMVar_ID_83711 Human_SNP_ID_687190427 m1A Human chr20 + 63958044 63958044 63958044 TGTGCGTGGGTGGGGGGAGTCCGGGTCTCCACACCCACTCCCTGGCACATCTGGCAAGGGCTGCT TGTGCGTGGGTGGGGGGAGTCCGGGTCTCCACGCCCACTCCCTGGCACATCTGGCAAGGGCTGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63957994..63958194 32194978 MeRIP-seq:(Medium) rs1326786884 Functional Loss SNV dbSNP153 33..33 33 - - - 83712 RMVar_ID_83712 Human_SNP_ID_687190766 m1A Human chr20 + 63959256 63959255 63959256 CACAGCAGGGATCGCACTGACAAAGGAGGAGCAGGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT CACAGCAGGGATCGCACTGACAAAGGAGGAGC_GGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:63959208..63959492;chr20:63959208..63959443 26863196 MeRIP-seq:(Medium) rs994993104 Functional Loss DEL dbSNP153 33..33 33 - - - 83713 RMVar_ID_83713 Human_SNP_ID_687190767 m1A Human chr20 + 63959256 63959256 63959256 CACAGCAGGGATCGCACTGACAAAGGAGGAGCAGGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT CACAGCAGGGATCGCACTGACAAAGGAGGAGCGGGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:63959208..63959492;chr20:63959208..63959443 26863196 MeRIP-seq:(Medium) rs1404421826 Functional Loss SNV dbSNP153 33..33 33 - - - 83714 RMVar_ID_83714 Human_SNP_ID_687190768 m1A Human chr20 + 63959256 63959256 63959256 CACAGCAGGGATCGCACTGACAAAGGAGGAGCAGGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT CACAGCAGGGATCGCACTGACAAAGGAGGAGCTGGGGTGGGGGTAGTGGGCAGGCCTGGAGAGGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:63959208..63959492;chr20:63959208..63959443 26863196 MeRIP-seq:(Medium) rs1404421826 Functional Loss SNV dbSNP153 33..33 33 - - - 83715 RMVar_ID_83715 Human_SNP_ID_687192862 m1A Human chr20 - 63964753 63964753 63964753 GCCACGGCCTGGGGGTAATGGGGCCCACAGTTAGGCCCTCCTGGCCCTCACCTCACCTGCTCCCT GCCACGGCCTGGGGGTAATGGGGCCCACAGTTTGGCCCTCCTGGCCCTCACCTCACCTGCTCCCT T A ZNF512B Ensembl:ENSG00000196700 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63964747..63964855 26863196 MeRIP-seq:(Medium) rs547085697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924253,Human_RBP_ID_1068226,Human_RBP_ID_5382812,Human_RBP_ID_22549618,Human_RBP_ID_22671761,Human_RBP_ID_22743778 RMVar_hsa_circ_22312 83716 RMVar_ID_83716 Human_SNP_ID_687193309 m1A Human chr20 + 63966332 63966332 63966332 TTGGTGACCGGCACGGGTTTCGTAACTGTCACAAGCTTTGTTACCGTAATGGGTTTGGTGACAGG TTGGTGACCGGCACGGGTTTCGTAACTGTCACGAGCTTTGTTACCGTAATGGGTTTGGTGACAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63966282..63966631 32194978 MeRIP-seq:(Medium) rs759111039 Functional Loss SNV dbSNP153 33..33 33 - - - 83717 RMVar_ID_83717 Human_SNP_ID_687193310 m1A Human chr20 + 63966332 63966332 63966332 TTGGTGACCGGCACGGGTTTCGTAACTGTCACAAGCTTTGTTACCGTAATGGGTTTGGTGACAGG TTGGTGACCGGCACGGGTTTCGTAACTGTCACTAGCTTTGTTACCGTAATGGGTTTGGTGACAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63966282..63966631 32194978 MeRIP-seq:(Medium) rs759111039 Functional Loss SNV dbSNP153 33..33 33 - - - 83718 RMVar_ID_83718 Human_SNP_ID_687194318 m1A Human chr20 - 63969580 63969580 63969580 CACTGCCTTCGCCCCCCCACCCCGCGCCCGCGATCGGCCCTGCCCGGCCAGGCCGAGGCCCGCGC CACTGCCTTCGCCCCCCCACCCCGCGCCCGCGGTCGGCCCTGCCCGGCCAGGCCGAGGCCCGCGC T C ZNF512B Ensembl:ENSG00000196700 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63969543..63969633 26863196 MeRIP-seq:(Medium) rs1442968757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244939 83719 RMVar_ID_83719 Human_SNP_ID_687194369 m1A Human chr20 - 63969682 63969682 63969682 GCCCGGAGCCCCCCCGCCCCCCGCCGCGCCCGAGCCCCCGCGCCCCGCGCCGGCGCCGTCTTCCT GCCCGGAGCCCCCCCGCCCCCCGCCGCGCCCGCGCCCCCGCGCCCCGCGCCGGCGCCGTCTTCCT T G ZNF512B Ensembl:ENSG00000196700 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:63969659..63969836 26863196 MeRIP-seq:(Medium) rs1246735031 Functional Loss SNV dbSNP153 33..33 33 - - - 83720 RMVar_ID_83720 Human_SNP_ID_687196118 m1A Human chr20 - 63974822 63974819 63974822 ATTGACCAAGCGCCAGAGACAAAATGTGGCACAACGAGAACCCCAGCCCTGTCCAGGTGGCTCCG ATTGACCAAGCGCCAGAGACAAAATGTGGCAC___GAGAACCCCAGCCCTGTCCAGGTGGCTCCG CGTT C SAMD10 Ensembl:ENSG00000130590 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63974772..63974882 26863196 MeRIP-seq:(Medium) rs879889813 Functional Loss DEL dbSNP153 33..35 33 - - - 83721 RMVar_ID_83721 Human_SNP_ID_687197535 m1A Human chr20 + 63979271 63979271 63979271 CCGTTGAGCCGAGACATCCGCCGAATACCCCCAGCCACCGCCGCTCGAAGCCCGCCGGGTCCCGC CCGTTGAGCCGAGACATCCGCCGAATACCCCCCGCCACCGCCGCTCGAAGCCCGCCGGGTCCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63979267..63979572 26863196 MeRIP-seq:(Medium) rs1433468150 Functional Loss SNV dbSNP153 33..33 33 - - - 83722 RMVar_ID_83722 Human_SNP_ID_687198455 m1A Human chr20 + 63981937 63981937 63981937 GCTTAATGGAGAGTAGCATTGGAGCCAAGTTTAGTAAGAGAGCTGGACTTAGGGCTGTAGAAACG GCTTAATGGAGAGTAGCATTGGAGCCAAGTTTGGTAAGAGAGCTGGACTTAGGGCTGTAGAAACG A G PRPF6 Ensembl:ENSG00000101161 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63981934..63982106 26863196 MeRIP-seq:(Medium) rs890255550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14171009 83723 RMVar_ID_83723 Human_SNP_ID_687208090 m1A Human chr20 - 64016772 64016772 64016772 CCTCAATCCCAATCCCAATCACGGCACGCATGACGGCCTGGCAGGTGGCCACACTCCCAGCCCTG CCTCAATCCCAATCCCAATCACGGCACGCATGGCGGCCTGGCAGGTGGCCACACTCCCAGCCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:64016669..64016899 26863196 MeRIP-seq:(Medium) rs756558140 Functional Loss SNV dbSNP153 33..33 33 - - - 83724 RMVar_ID_83724 Human_SNP_ID_687211194 m1A Human chr20 + 64027032 64027032 64027032 AAGCTGGAGTGGGTGCAAGACAACATCAGGGCAGCCCAAGATCTGTGCGAGGAGGCCCTGCGGCA AAGCTGGAGTGGGTGCAAGACAACATCAGGGCCGCCCAAGATCTGTGCGAGGAGGCCCTGCGGCA A C PRPF6 Ensembl:ENSG00000101161 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:64026941..64027187;chr20:64026948..64027175;chr20:64026949..64027098 26863196 MeRIP-seq:(Medium) rs774301488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2105494 Human_miRNA_ID_3091388 RMVar_hsa_circ_933,RMVar_hsa_circ_45960,RMVar_hsa_circ_123569,RMVar_hsa_circ_211371,RMVar_hsa_circ_77707,RMVar_hsa_circ_211372,RMVar_hsa_circ_88388,RMVar_hsa_circ_211377,RMVar_hsa_circ_211374,RMVar_hsa_circ_211375,RMVar_hsa_circ_79542,RMVar_hsa_circ_121424,RMVar_hsa_circ_25340,RMVar_hsa_circ_211381,RMVar_hsa_circ_87852,RMVar_hsa_circ_24322,RMVar_hsa_circ_211384,RMVar_hsa_circ_106583,RMVar_hsa_circ_349041,RMVar_hsa_circ_90956,RMVar_hsa_circ_211386,RMVar_hsa_circ_211385,RMVar_hsa_circ_125386,RMVar_hsa_circ_211391 83725 RMVar_ID_83725 Human_SNP_ID_687213003 m1A Human chr20 + 64032997 64032997 64032997 TGGCCGGCCGCATCAAGAACACCTTCTGATTGAGCGGTTGCCATGGCCGGTCTCCGTGGGGCAGG TGGCCGGCCGCATCAAGAACACCTTCTGATTGGGCGGTTGCCATGGCCGGTCTCCGTGGGGCAGG A G PRPF6 Ensembl:ENSG00000101161 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:64032951..64033000 32194978 MeRIP-seq:(Medium) rs1299238942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62344,Human_RBP_ID_17659141,Human_RBP_ID_21983930,Human_RBP_ID_22507095,Human_RBP_ID_23004632 RMVar_hsa_circ_77707,RMVar_hsa_circ_211372,RMVar_hsa_circ_88388,RMVar_hsa_circ_211377,RMVar_hsa_circ_211375,RMVar_hsa_circ_79542,RMVar_hsa_circ_121424,RMVar_hsa_circ_211381,RMVar_hsa_circ_87852,RMVar_hsa_circ_211384,RMVar_hsa_circ_106583,RMVar_hsa_circ_211385,RMVar_hsa_circ_123547,RMVar_hsa_circ_125386,RMVar_hsa_circ_211391,RMVar_hsa_circ_211393,RMVar_hsa_circ_211394,RMVar_hsa_circ_128130 83726 RMVar_ID_83726 Human_SNP_ID_687217437 m1A Human chr20 + 64048095 64048095 64048095 AAACATACACGCGTATGAGAGAGCAGAGCGGCAGCGACGCGGTCGGATCGGTCGCGGGGGCTGCG AAACATACACGCGTATGAGAGAGCAGAGCGGCGGCGACGCGGTCGGATCGGTCGCGGGGGCTGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:64047957..64048203 26863196 MeRIP-seq:(Medium) rs1314708171 Functional Loss SNV dbSNP153 33..33 33 - - - 83727 RMVar_ID_83727 Human_SNP_ID_687217496 m1A Human chr20 - 64048209 64048209 64048209 AGAGGAGAGCAGCCTGATCTCCGCGCTGTCGGACGCCAGCAGCGCGGTCTATTACAGCGCGTGCA AGAGGAGAGCAGCCTGATCTCCGCGCTGTCGGCCGCCAGCAGCGCGGTCTATTACAGCGCGTGCA T G SOX18 Ensembl:ENSG00000203883 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:64048120..64048366 26863410 MeRIP-seq:(Medium) rs1368939952 Functional Loss SNV dbSNP153 33..33 33 - - - 83728 RMVar_ID_83728 Human_SNP_ID_687217819 m1A Human chr20 + 64048885 64048885 64048885 CGGCCGGTACTTGTAGTTGGGGTGGTCGCGCAAGTGCTGCACGCGCAGCCGTTCGGCTTCCTCCA CGGCCGGTACTTGTAGTTGGGGTGGTCGCGCAGGTGCTGCACGCGCAGCCGTTCGGCTTCCTCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:64048807..64048906 26863410 MeRIP-seq:(Medium) rs780769626 Functional Loss SNV dbSNP153 33..33 33 - - - 83729 RMVar_ID_83729 Human_SNP_ID_687218007 m1A Human chr20 - 64049146 64049146 64049146 GGTGCTCAGCAAGATGCTGGGTGAGCGGCGGGAGGGCGGCAGAGAAGGGGGAGAGGGCGGGGGGG GGTGCTCAGCAAGATGCTGGGTGAGCGGCGGGGGGGCGGCAGAGAAGGGGGAGAGGGCGGGGGGG T C SOX18 Ensembl:ENSG00000203883 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:64049144..64049249 26863196 MeRIP-seq:(Medium) rs748024342 Functional Loss SNV dbSNP153 33..33 33 - - - 83730 RMVar_ID_83730 Human_SNP_ID_687218008 m1A Human chr20 - 64049146 64049146 64049146 GGTGCTCAGCAAGATGCTGGGTGAGCGGCGGGAGGGCGGCAGAGAAGGGGGAGAGGGCGGGGGGG GGTGCTCAGCAAGATGCTGGGTGAGCGGCGGGCGGGCGGCAGAGAAGGGGGAGAGGGCGGGGGGG T G SOX18 Ensembl:ENSG00000203883 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:64049144..64049249 26863196 MeRIP-seq:(Medium) rs748024342 Functional Loss SNV dbSNP153 33..33 33 - - - 83731 RMVar_ID_83731 Human_SNP_ID_687219297 m1A Human chr20 - 64053490 64053489 64053490 GACACCTGACACCACACGACGACTGGCACATCACCCCTTAGACTACAAAAGCACCCCACTCACAC GACACCTGACACCACACGACGACTGGCACATC_CCCCTTAGACTACAAAAGCACCCCACTCACAC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:64053485..64053564 26863196 MeRIP-seq:(Medium) rs1327129843 Functional Loss DEL dbSNP153 33..33 33 - - - 83732 RMVar_ID_83732 Human_SNP_ID_687222207 m1A Human chr20 - 64063314 64063314 64063314 CGATCCGCGCAATCTCCTCTTCCTTGCCCATCATCGCCTCAGGAGCAGCGACCCCCGCGCCCGTC CGATCCGCGCAATCTCCTCTTCCTTGCCCATCCTCGCCTCAGGAGCAGCGACCCCCGCGCCCGTC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:64063215..64063427 26863196 MeRIP-seq:(Medium) rs1316342529 Functional Loss SNV dbSNP153 33..33 33 - - - 83733 RMVar_ID_83733 Human_SNP_ID_687222322 m1A Human chr20 + 64063587 64063587 64063587 GCCCCGGGCCAGCCCTGCCGTTCACTCCCGCAACCCCGGCAGAGGCCGCGATCAGGCCTGGACCT GCCCCGGGCCAGCCCTGCCGTTCACTCCCGCAGCCCCGGCAGAGGCCGCGATCAGGCCTGGACCT A G TCEA2 Ensembl:ENSG00000171703 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:64063434..64063818 26863196 MeRIP-seq:(Medium) rs1170843453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116610,RMVar_hsa_circ_211396 83734 RMVar_ID_83734 Human_SNP_ID_687223491 m1A Human chr20 + 64067342 64067342 64067342 CTGACAGCACTGAGAGACTGGGGTGAGTTGGGAGGTCACACAGAGGGGAAGGTCATGGCCAGGAG CTGACAGCACTGAGAGACTGGGGTGAGTTGGGGGGTCACACAGAGGGGAAGGTCATGGCCAGGAG A G TCEA2 Ensembl:ENSG00000171703 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:64067239..64067454 26863196 MeRIP-seq:(Medium) rs957974017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10122,RMVar_hsa_circ_116610,RMVar_hsa_circ_3498,RMVar_hsa_circ_211396,RMVar_hsa_circ_52318,RMVar_hsa_circ_79154,RMVar_hsa_circ_109578,RMVar_hsa_circ_211397,RMVar_hsa_circ_211398 83735 RMVar_ID_83735 Human_SNP_ID_687224362 m1A Human chr20 - 64070186 64070186 64070186 CCCTCCACCTACCACCTGCCCCGCTGGGGGCCATGTTGGGGTGGGGGCTGGAAAGGTTCTGCCCA CCCTCCACCTACCACCTGCCCCGCTGGGGGCCGTGTTGGGGTGGGGGCTGGAAAGGTTCTGCCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:64070184..64070284 32194978 MeRIP-seq:(Medium) rs182345558 Functional Loss SNV dbSNP153 33..33 33 - - - 83736 RMVar_ID_83736 Human_SNP_ID_687224501 m1A Human chr20 + 64070582 64070582 64070582 AGCACCAGATGGCCCGCACTGGCGGCACGCAGACAGACCTGTTCACCTGCGGCAAGTGCAGGAAA AGCACCAGATGGCCCGCACTGGCGGCACGCAGGCAGACCTGTTCACCTGCGGCAAGTGCAGGAAA A G TCEA2 Ensembl:ENSG00000171703 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:64070481..64070581 32194978 MeRIP-seq:(Medium) rs1275639853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569032 Human_Splice_Rec_2105542,Human_Splice_Rec_2105543,Human_Splice_Rec_2105567,Human_Splice_Rec_2105584,Human_Splice_Rec_2105585,Human_Splice_Rec_2105602,Human_Splice_Rec_2105620,Human_Splice_Rec_2105638,Human_Splice_Rec_2105639,Human_Splice_Rec_2105654,Human_Splice_Rec_2105655,Human_Splice_Rec_2105660,Human_Splice_Rec_2105661,Human_Splice_Rec_2105666,Human_Splice_Rec_2105667,Human_Splice_Rec_2105671,Human_Splice_Rec_2105675,Human_Splice_Rec_2105678,Human_Splice_Rec_2105679 RMVar_hsa_circ_10122,RMVar_hsa_circ_116610,RMVar_hsa_circ_3498,RMVar_hsa_circ_211396,RMVar_hsa_circ_26251,RMVar_hsa_circ_52318,RMVar_hsa_circ_79154,RMVar_hsa_circ_109578,RMVar_hsa_circ_211397,RMVar_hsa_circ_114434,RMVar_hsa_circ_211398,RMVar_hsa_circ_105050,RMVar_hsa_circ_211399,RMVar_hsa_circ_120265,RMVar_hsa_circ_211400,RMVar_hsa_circ_110736,RMVar_hsa_circ_211401,RMVar_hsa_circ_211402 83737 RMVar_ID_83737 Human_SNP_ID_687226359 m1A Human chr20 + 64076609 64076609 64076609 GGGCCGCTGGAGAGGCTGTATCATGACTGGACATTGAAGGGGGCCGGTCCGCCTCCTCTGGCCCT GGGCCGCTGGAGAGGCTGTATCATGACTGGACGTTGAAGGGGGCCGGTCCGCCTCCTCTGGCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:64076570..64076667 26863196 MeRIP-seq:(Medium) rs1375975193 Functional Loss SNV dbSNP153 33..33 33 - - - 83738 RMVar_ID_83738 Human_SNP_ID_687232631 m1A Human chr20 + 64096727 64096719 64096728 TCATCATCACAATCATCACCATCACCACCATCATCACCACTATCATCATCACCACTATCACCACC TCATCATCACAATCATCACCATCAC_________CACCACTATCATCATCACCACTATCACCACC CCACCATCAT C OPRL1 Ensembl:ENSG00000125510 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:64096721..64096817 26863196 MeRIP-seq:(Medium) rs1268455893 Functional Loss DEL dbSNP153 26..34 33 - - - 83739 RMVar_ID_83739 Human_SNP_ID_687232638 m1A Human chr20 + 64096727 64096727 64096727 TCATCATCACAATCATCACCATCACCACCATCATCACCACTATCATCATCACCACTATCACCACC TCATCATCACAATCATCACCATCACCACCATCGTCACCACTATCATCATCACCACTATCACCACC A G OPRL1 Ensembl:ENSG00000125510 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:64096721..64096817 26863196 MeRIP-seq:(Medium) rs1309982751 Functional Loss SNV dbSNP153 33..33 33 - - - 83740 RMVar_ID_83740 Human_SNP_ID_687278041 m1A Human chr20 + 64256013 64256013 64256013 GGAGCTCTCCTCTGGGGGCGTCGCTCCTCCCCACCTCGGGCACCCTCACCTCCCCCCAGCGGCCT GGAGCTCTCCTCTGGGGGCGTCGCTCCTCCCCCCCTCGGGCACCCTCACCTCCCCCCAGCGGCCT A C PCMTD2 Ensembl:ENSG00000203880 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:64255919..64256097 26863196 MeRIP-seq:(Medium) rs1415499005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244628,Human_RBP_ID_1199192,Human_RBP_ID_5132352,Human_RBP_ID_5503724,Human_RBP_ID_9331730,Human_RBP_ID_17086260,Human_RBP_ID_18951933,Human_RBP_ID_23917012,Human_RBP_ID_27488740 RMVar_hsa_circ_211406,RMVar_hsa_circ_115537 83741 RMVar_ID_83741 Human_SNP_ID_687281953 m1A Human chr20 + 64270337 64270337 64270337 GGGATCGTGTGAGTGCACAGTGGGTTGTGTGGACGTGCACGGTGTGGCGTCGTGAGTTCAGGCAT GGGATCGTGTGAGTGCACAGTGGGTTGTGTGGGCGTGCACGGTGTGGCGTCGTGAGTTCAGGCAT A G PCMTD2 Ensembl:ENSG00000203880 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:64270064..64270415 26863196 MeRIP-seq:(Medium) rs1442253844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830953,Human_RBP_ID_3656584,Human_RBP_ID_5296862,Human_RBP_ID_5652471,Human_RBP_ID_8113692,Human_RBP_ID_8204458,Human_RBP_ID_17283259,Human_RBP_ID_21983300,Human_RBP_ID_22478960,Human_RBP_ID_23115394,Human_RBP_ID_23918069,Human_RBP_ID_26770566 RMVar_hsa_circ_211407 83742 RMVar_ID_83742 Human_SNP_ID_687282765 m1A Human chr20 - 64273406 64273406 64273406 GTCATCTGAGGGGTTGGAAATCCGACTGGCAAAGACTTCTTTGTCCAAAAAGACAATCGTTTCCA GTCATCTGAGGGGTTGGAAATCCGACTGGCAAGGACTTCTTTGTCCAAAAAGACAATCGTTTCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:64273355..64273600 26863196 MeRIP-seq:(Medium) rs772040163 Functional Loss SNV dbSNP153 33..33 33 - - - 83743 RMVar_ID_83743 Human_SNP_ID_479182617 m1A Human chr11 - 100879697 100879697 100879697 GGTGATTAGGGACAGTGAAGAAAGGTAAGAACAGGGTAGATGAGGCAGGGAGGTCGCAGCTCACA GGTGATTAGGGACAGTGAAGAAAGGTAAGAACGGGGTAGATGAGGCAGGGAGGTCGCAGCTCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:100879551..100879802;chr11:100879647..100879778 26863196 MeRIP-seq:(Medium) rs891436056 Functional Loss SNV dbSNP153 33..33 33 - - - 83744 RMVar_ID_83744 Human_SNP_ID_479444343 m1A Human chr11 + 101889248 101889244 101889248 AAAGAAGAAAAAGAAAGAAAGGAAGAAAGAGGAAGGAAGGAAGGGAGGGAGGGAAAGGAAAGAAA AAAGAAGAAAAAGAAAGAAAGGAAGAAAG____AGGAAGGAAGGGAGGGAGGGAAAGGAAAGAAA GAGGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:101889213..101889374 26863196 MeRIP-seq:(Medium) rs367648222 Functional Loss DEL dbSNP153 30..33 33 - - - 83745 RMVar_ID_83745 Human_SNP_ID_479444431 m1A Human chr11 + 101889365 101889365 101889365 AGAGAAAGAAAGAAGAAAAAAGAAAGAAAGAAAAAAGAAAGGAAGAGAAAGAAAGAAAGAAAAAA AGAGAAAGAAAGAAGAAAAAAGAAAGAAAGAAGAAAGAAAGGAAGAGAAAGAAAGAAAGAAAAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:101889152..101889468 26863196 MeRIP-seq:(Medium) rs58807837 Functional Loss SNV dbSNP153 33..33 33 - - - 83746 RMVar_ID_83746 Human_SNP_ID_479444433 m1A Human chr11 + 101889368 101889365 101889369 GAAAGAAAGAAGAAAAAAGAAAGAAAGAAAAAAGAAAGGAAGAGAAAGAAAGAAAGAAAAAAGAG GAAAGAAAGAAGAAAAAAGAAAGAAAGAAA____AAAGGAAGAGAAAGAAAGAAAGAAAAAAGAG AAAAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:101889149..101889472 26863196 MeRIP-seq:(Medium) rs1183017084 Functional Loss DEL dbSNP153 31..34 33 - - - 83747 RMVar_ID_83747 Human_SNP_ID_479444435 m1A Human chr11 + 101889368 101889366 101889369 GAAAGAAAGAAGAAAAAAGAAAGAAAGAAAAAAGAAAGGAAGAGAAAGAAAGAAAGAAAAAAGAG GAAAGAAAGAAGAAAAAAGAAAGAAAGAAAA___AAAGGAAGAGAAAGAAAGAAAGAAAAAAGAG AAAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:101889149..101889472 26863196 MeRIP-seq:(Medium) rs1369720271 Functional Loss DEL dbSNP153 32..34 33 - - - 83748 RMVar_ID_83748 Human_SNP_ID_479451256 m1A Human chr11 + 101915265 101915265 101915265 TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACAGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACCGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA A C CEP126 Ensembl:ENSG00000110318 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:101915172..101915358 26863196 MeRIP-seq:(Medium) rs368939235 Functional Loss SNV dbSNP153 33..33 33 - - - 83749 RMVar_ID_83749 Human_SNP_ID_479451257 m1A Human chr11 + 101915265 101915265 101915265 TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACAGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACGGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA A G CEP126 Ensembl:ENSG00000110318 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:101915172..101915358 26863196 MeRIP-seq:(Medium) rs368939235 Functional Loss SNV dbSNP153 33..33 33 - - - 83750 RMVar_ID_83750 Human_SNP_ID_479451258 m1A Human chr11 + 101915265 101915265 101915265 TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACAGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA TGCCATGAGGGAGGTTCTGGGGGCGAGCAGACTGGCGGCGCTGAAGTGAAGGATGCTGGCGGGGA A T CEP126 Ensembl:ENSG00000110318 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:101915172..101915358 26863196 MeRIP-seq:(Medium) rs368939235 Functional Loss SNV dbSNP153 33..33 33 - - - 83751 RMVar_ID_83751 Human_SNP_ID_479453116 m1A Human chr11 + 101922692 101922692 101922692 GAGAAAAATTTAGAAGAAGAGCGCCAGATATTACTGCAGCAACAAAAAATATGTCGAAATCGAGC GAGAAAAATTTAGAAGAAGAGCGCCAGATATTCCTGCAGCAACAAAAAATATGTCGAAATCGAGC A C CEP126 Ensembl:ENSG00000110318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:101922603..101922705 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1291090,Human_Splice_Rec_1291091,Human_Splice_Rec_1291110,Human_Splice_Rec_1291111,Human_Splice_Rec_1291132,Human_Splice_Rec_1291133 83752 RMVar_ID_83752 Human_SNP_ID_479498394 m1A Human chr11 - 102110322 102110322 102110322 TGCGCGCCCGCCCGCACCGCGGCCCGGCCGGCAGCGCAGGGAAACTTTTCGCTGCAAGTTGCTAC TGCGCGCCCGCCCGCACCGCGGCCCGGCCGGCCGCGCAGGGAAACTTTTCGCTGCAAGTTGCTAC T G AP001527.2 Ensembl:ENSG00000277459 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:102110276..102110425 26863196 MeRIP-seq:(Medium) rs1295986983 Functional Loss SNV dbSNP153 33..33 33 - - - 83753 RMVar_ID_83753 Human_SNP_ID_479498709 m1A Human chr11 + 102111003 102111003 102111003 CCAGGCGGCGCCGCAGGCACCCCCCGCCGGGCATCAGATCGTGCACGTCCGCGGGGACTCGGAGA CCAGGCGGCGCCGCAGGCACCCCCCGCCGGGCCTCAGATCGTGCACGTCCGCGGGGACTCGGAGA A C YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:102110451..102111270 26863196 MeRIP-seq:(Medium) rs1489749556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109018,Human_RBP_ID_4145378 83754 RMVar_ID_83754 Human_SNP_ID_479498710 m1A Human chr11 + 102111003 102111003 102111003 CCAGGCGGCGCCGCAGGCACCCCCCGCCGGGCATCAGATCGTGCACGTCCGCGGGGACTCGGAGA CCAGGCGGCGCCGCAGGCACCCCCCGCCGGGCTTCAGATCGTGCACGTCCGCGGGGACTCGGAGA A T YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:102110451..102111270 26863196 MeRIP-seq:(Medium) rs1489749556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109018,Human_RBP_ID_4145378 83755 RMVar_ID_83755 Human_SNP_ID_479499775 m1A Human chr11 + 102114158 102114158 102114158 CTTAATATTCCCTAATAGGCCAGTACTGATGCAGGCACTGCAGGAGCCCTGACTCCACAGCATGT CTTAATATTCCCTAATAGGCCAGTACTGATGCGGGCACTGCAGGAGCCCTGACTCCACAGCATGT A G YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:102114126..102114200 26863196 MeRIP-seq:(Medium) rs776181734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_869777,Human_RBP_ID_9362880,Human_RBP_ID_17467144 Human_Splice_Rec_1291218,Human_Splice_Rec_1291234,Human_Splice_Rec_1291246,Human_Splice_Rec_1291260,Human_Splice_Rec_1291276,Human_Splice_Rec_1291290,Human_Splice_Rec_1291302,Human_Splice_Rec_1291316 Human_miRNA_ID_2353668 RMVar_hsa_circ_72538,RMVar_hsa_circ_317338,RMVar_hsa_circ_326089,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_152659 83756 RMVar_ID_83756 Human_SNP_ID_479522293 m1A Human chr11 - 102199015 102199015 102199015 TCTCCTTCTCCTCCACAAACACATAGACATACACATACATTCTCTCTCTCCCTCCTCCTATTTTA TCTCCTTCTCCTCCACAAACACATAGACATACTCATACATTCTCTCTCTCCCTCCTCCTATTTTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:102199011..102199089 26863196 MeRIP-seq:(Medium) rs1432142296 Functional Loss SNV dbSNP153 33..33 33 - - - 83757 RMVar_ID_83757 Human_SNP_ID_479527701 m1A Human chr11 - 102220607 102220604 102220607 AGTCTAGTCTATTGGCTGTCTTTTGGTATCTTATTTTTTTTTCTCCTTCCCTACAAGCTTAAATT AGTCTAGTCTATTGGCTGTCTTTTGGTATCTT___TTTTTTTCTCCTTCCCTACAAGCTTAAATT AAAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:102220601..102220822 26863196 MeRIP-seq:(Medium) rs1021225401 Functional Loss DEL dbSNP153 33..35 33 - - - 83758 RMVar_ID_83758 Human_SNP_ID_479527707 m1A Human chr11 + 102220613 102220613 102220613 AGCTTGTAGGGAAGGAGAAAAAAAAATAAGATACCAAAAGACAGCCAATAGACTAGACTAGTAAG AGCTTGTAGGGAAGGAGAAAAAAAAATAAGATGCCAAAAGACAGCCAATAGACTAGACTAGTAAG A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102220608..102220851 26863196 MeRIP-seq:(Medium) rs967609598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337147,RMVar_hsa_circ_367842,RMVar_hsa_circ_339348,RMVar_hsa_circ_43277,RMVar_hsa_circ_313881,RMVar_hsa_circ_283650,RMVar_hsa_circ_152663,RMVar_hsa_circ_152662 83759 RMVar_ID_83759 Human_SNP_ID_479529024 m1A Human chr11 + 102225586 102225586 102225586 TATTCCTTAAGCTCTAAATACTTTTTGCCCCAACTTGCCTTGGCATTGACTCTTAGTAGTAATGC TATTCCTTAAGCTCTAAATACTTTTTGCCCCAGCTTGCCTTGGCATTGACTCTTAGTAGTAATGC A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:102225551..102225775 26863196 MeRIP-seq:(Medium) rs532688129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43277,RMVar_hsa_circ_313881,RMVar_hsa_circ_340944,RMVar_hsa_circ_152662,RMVar_hsa_circ_152667 83760 RMVar_ID_83760 Human_SNP_ID_479529026 m1A Human chr11 - 102225600 102225600 102225600 ACTAAGGGAACTCAGCATTACTACTAAGAGTCAATGCCAAGGCAAGTTGGGGCAAAAAGTATTTA ACTAAGGGAACTCAGCATTACTACTAAGAGTCTATGCCAAGGCAAGTTGGGGCAAAAAGTATTTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:102225551..102225625 26863196 MeRIP-seq:(Medium) rs573308640 Functional Loss SNV dbSNP153 33..33 33 - - - 83761 RMVar_ID_83761 Human_SNP_ID_479530070 m1A Human chr11 + 102229751 102229751 102229751 AGCACCCTGCCCTCACAGCAGAACCGTTTCCCAGACTACCTTGAAGCCATTCCTGGGACAAATGT AGCACCCTGCCCTCACAGCAGAACCGTTTCCCGGACTACCTTGAAGCCATTCCTGGGACAAATGT A G YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:102229680..102229773 26863196 MeRIP-seq:(Medium) rs201530575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17235315 Human_Splice_Rec_1291232,Human_Splice_Rec_1291244,Human_Splice_Rec_1291258,Human_Splice_Rec_1291274,Human_Splice_Rec_1291288,Human_Splice_Rec_1291300,Human_Splice_Rec_1291314,Human_Splice_Rec_1291330,Human_Splice_Rec_1291342,Human_Splice_Rec_1291346 Human_miRNA_ID_2043244,Human_miRNA_ID_2045394,Human_miRNA_ID_2168427,Human_miRNA_ID_2169950 83762 RMVar_ID_83762 Human_SNP_ID_479530071 m1A Human chr11 + 102229751 102229751 102229751 AGCACCCTGCCCTCACAGCAGAACCGTTTCCCAGACTACCTTGAAGCCATTCCTGGGACAAATGT AGCACCCTGCCCTCACAGCAGAACCGTTTCCCTGACTACCTTGAAGCCATTCCTGGGACAAATGT A T YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:102229680..102229773 26863196 MeRIP-seq:(Medium) rs201530575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17235315 Human_Splice_Rec_1291232,Human_Splice_Rec_1291244,Human_Splice_Rec_1291258,Human_Splice_Rec_1291274,Human_Splice_Rec_1291288,Human_Splice_Rec_1291300,Human_Splice_Rec_1291314,Human_Splice_Rec_1291330,Human_Splice_Rec_1291342,Human_Splice_Rec_1291346 Human_miRNA_ID_2043244,Human_miRNA_ID_2045394,Human_miRNA_ID_2168427,Human_miRNA_ID_2169950 83763 RMVar_ID_83763 Human_SNP_ID_479533698 m1A Human chr11 + 102243640 102243640 102243640 AGAAGGAAGGGAAGGAAGAGAAAAAGAGAAAGAGAAGAAAGAAAGGAAGAAAGAAAGAGAAAGGA AGAAGGAAGGGAAGGAAGAGAAAAAGAGAAAGCGAAGAAAGAAAGGAAGAAAGAAAGAGAAAGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:102243590..102243687 26863196 MeRIP-seq:(Medium) rs754840049 Functional Loss SNV dbSNP153 33..33 33 - - - 83764 RMVar_ID_83764 Human_SNP_ID_479552001 m1A Human chr11 - 102317594 102317588 102317594 ATACACACACACACACGCACACACACACACACACACACCAGCCTTCCTTGCCCACCTGCTGCCCA ATACACACACACACACGCACACACACACACAC______CAGCCTTCCTTGCCCACCTGCTGCCCA GGTGTGT G AP000942.5 Ensembl:ENSG00000288528 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102317574..102317734 26863196 MeRIP-seq:(Medium) rs57970279 Functional Loss DEL dbSNP153 33..38 33 - - - 83765 RMVar_ID_83765 Human_SNP_ID_479552002 m1A Human chr11 - 102317594 102317588 102317594 ATACACACACACACACGCACACACACACACACACACACCAGCCTTCCTTGCCCACCTGCTGCCCA ATACACACACACACACGCACACACACACACAC____ACCAGCCTTCCTTGCCCACCTGCTGCCCA GGTGTGT GGT AP000942.5 Ensembl:ENSG00000288528 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102317574..102317734 26863196 MeRIP-seq:(Medium) rs57970279 Functional Loss DEL dbSNP153 33..36 33 - - - 83766 RMVar_ID_83766 Human_SNP_ID_479552003 m1A Human chr11 - 102317594 102317588 102317594 ATACACACACACACACGCACACACACACACACACACACCAGCCTTCCTTGCCCACCTGCTGCCCA ATACACACACACACACGCACACACACACACAC__ACACCAGCCTTCCTTGCCCACCTGCTGCCCA GGTGTGT GGTGT AP000942.5 Ensembl:ENSG00000288528 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102317574..102317734 26863196 MeRIP-seq:(Medium) rs57970279 Functional Loss DEL dbSNP153 33..34 33 - - - 83767 RMVar_ID_83767 Human_SNP_ID_479553340 m1A Human chr11 - 102322907 102322907 102322907 AAAATAATAAATTTACCATTTCAACAGCAGAGACCTTGTCAAAATTCAGAATTTCTCAATTATGA AAAATAATAAATTTACCATTTCAACAGCAGAGTCCTTGTCAAAATTCAGAATTTCTCAATTATGA T A AP000942.5 Ensembl:ENSG00000288528 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:102322863..102322943 32194978 MeRIP-seq:(Medium) rs17879707 Functional Loss SNV dbSNP153 33..33 33 - - - 83768 RMVar_ID_83768 Human_SNP_ID_479553341 m1A Human chr11 - 102322907 102322907 102322907 AAAATAATAAATTTACCATTTCAACAGCAGAGACCTTGTCAAAATTCAGAATTTCTCAATTATGA AAAATAATAAATTTACCATTTCAACAGCAGAGGCCTTGTCAAAATTCAGAATTTCTCAATTATGA T C AP000942.5 Ensembl:ENSG00000288528 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:102322863..102322943 32194978 MeRIP-seq:(Medium) rs17879707 Functional Loss SNV dbSNP153 33..33 33 - - - 83769 RMVar_ID_83769 Human_SNP_ID_479559473 m1A Human chr11 + 102347275 102347275 102347275 CGGCGGGCTTCGGGAGCGCCCGGGCTGATCCGAGCCGAGCGGGCCGTATCTCCTTGTCGGCGCCG CGGCGGGCTTCGGGAGCGCCCGGGCTGATCCGTGCCGAGCGGGCCGTATCTCCTTGTCGGCGCCG A T BIRC2 Ensembl:ENSG00000110330 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:102347226..102347397 26863196 MeRIP-seq:(Medium) rs927017612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184389,Human_RBP_ID_5435946,Human_RBP_ID_18416655,Human_RBP_ID_22895599,Human_RBP_ID_23117988 RMVar_hsa_circ_75948,RMVar_hsa_circ_152670 83770 RMVar_ID_83770 Human_SNP_ID_479559493 m1A Human chr11 - 102347296 102347296 102347296 CTCCGCAGAGCCGGGAATCAGCGGCGCCGACAAGGAGATACGGCCCGCTCGGCTCGGATCAGCCC CTCCGCAGAGCCGGGAATCAGCGGCGCCGACATGGAGATACGGCCCGCTCGGCTCGGATCAGCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:102347246..102347376;chr11:102347247..102347360 26863196 MeRIP-seq:(Medium) rs1039822426 Functional Loss SNV dbSNP153 33..33 33 - - - 83771 RMVar_ID_83771 Human_SNP_ID_479575818 m1A Human chr11 - 102402120 102402120 102402120 TGAAACCACCAACTTCAGTTGCCTCAGACTCCAGTAATACAACGGTCACCACCATGAAACCTACA TGAAACCACCAACTTCAGTTGCCTCAGACTCCGGTAATACAACGGTCACCACCATGAAACCTACA T C TMEM123 Ensembl:ENSG00000152558 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:102402070..102402160 26863196 MeRIP-seq:(Medium) rs780939258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32441,Human_RBP_ID_1774608,Human_RBP_ID_6036801,Human_RBP_ID_11504259,Human_RBP_ID_17183931,Human_RBP_ID_17230645,Human_RBP_ID_17467029,Human_RBP_ID_24458531,Human_RBP_ID_26804051,Human_RBP_ID_27197266 Human_Splice_Rec_1291588,Human_Splice_Rec_1291594,Human_Splice_Rec_1291602,Human_Splice_Rec_1291610,Human_Splice_Rec_1291618,Human_Splice_Rec_1291622,Human_Splice_Rec_1291626,Human_Splice_Rec_1291632 RMVar_hsa_circ_361869 83772 RMVar_ID_83772 Human_SNP_ID_479575851 m1A Human chr11 + 102402200 102402200 102402200 TTTCATTTGTATGGTCAGAAGGCACATGTTGGAGAGTCTCTGCAATAATATCAAGAAACATTAAA TTTCATTTGTATGGTCAGAAGGCACATGTTGGGGAGTCTCTGCAATAATATCAAGAAACATTAAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:102402176..102402200 26863196 MeRIP-seq:(Medium) rs1177009147 Functional Loss SNV dbSNP153 33..33 33 - - - 83773 RMVar_ID_83773 Human_SNP_ID_479588225 m1A Human chr11 - 102448827 102448827 102448827 ACATAGAGAATTCTGGGCTTCCACACAACTCCAGTGCTAACTCAACAGGTGAGTTTTAAAAGATT ACATAGAGAATTCTGGGCTTCCACACAACTCCGGTGCTAACTCAACAGGTGAGTTTTAAAAGATT T C TMEM123 Ensembl:ENSG00000152558 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:102448826..102448875 26863196 MeRIP-seq:(Medium) rs1251416421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_387482,Human_RBP_ID_1453499,Human_RBP_ID_1774612,Human_RBP_ID_3366615,Human_RBP_ID_4145596,Human_RBP_ID_6036899,Human_RBP_ID_8343493,Human_RBP_ID_8766153,Human_RBP_ID_17183933,Human_RBP_ID_17230649,Human_RBP_ID_17347127,Human_RBP_ID_17462492,Human_RBP_ID_17681130,Human_RBP_ID_17788492,Human_RBP_ID_18602023,Human_RBP_ID_22433918,Human_RBP_ID_22642007 Human_Splice_Rec_1291586,Human_Splice_Rec_1291587,Human_Splice_Rec_1291600,Human_Splice_Rec_1291601,Human_Splice_Rec_1291608,Human_Splice_Rec_1291609,Human_Splice_Rec_1291616,Human_Splice_Rec_1291617,Human_Splice_Rec_1291620,Human_Splice_Rec_1291621,Human_Splice_Rec_1291624,Human_Splice_Rec_1291625,Human_Splice_Rec_1291628,Human_Splice_Rec_1291629 RMVar_hsa_circ_38796 83774 RMVar_ID_83774 Human_SNP_ID_479591380 m1A Human chr11 + 102461628 102461628 102461628 GGTGGGAAGAAAGAAGGAATAGAAGCCAAAGGAAGGGGGATGAAAAGCAAAACCAAGAATCACAA GGTGGGAAGAAAGAAGGAATAGAAGCCAAAGGCAGGGGGATGAAAAGCAAAACCAAGAATCACAA A C AP001830.1 Ensembl:ENSG00000255337 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:102461593..102461659 26863196 MeRIP-seq:(Medium) rs1385330590 Functional Loss SNV dbSNP153 33..33 33 - - - 83775 RMVar_ID_83775 Human_SNP_ID_479693685 m1A Human chr11 - 102843553 102843553 102843553 GGCATAGAGACAACATAGAGCTAAGTAAAGCCAGTGGAAATGAAGAGTCTTCCAATCCTACTGTT GGCATAGAGACAACATAGAGCTAAGTAAAGCCGGTGGAAATGAAGAGTCTTCCAATCCTACTGTT T C MMP3 Ensembl:ENSG00000149968 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102843505..102843588 26863196 MeRIP-seq:(Medium) rs368234859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1291907 83776 RMVar_ID_83776 Human_SNP_ID_479693686 m1A Human chr11 - 102843553 102843553 102843553 GGCATAGAGACAACATAGAGCTAAGTAAAGCCAGTGGAAATGAAGAGTCTTCCAATCCTACTGTT GGCATAGAGACAACATAGAGCTAAGTAAAGCCCGTGGAAATGAAGAGTCTTCCAATCCTACTGTT T G MMP3 Ensembl:ENSG00000149968 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:102843505..102843588 26863196 MeRIP-seq:(Medium) rs368234859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1291907 83777 RMVar_ID_83777 Human_SNP_ID_480213839 m1A Human chr11 - 104968473 104968472 104968474 TGACTAGGAGTTTGGGAGTAGGAACTTAGAAAACACTTGATTTATTGCTCTGAAATAAACACAAG TGACTAGGAGTTTGGGAGTAGGAACTTAGAA__CACTTGATTTATTGCTCTGAAATAAACACAAG GTT G CASP4 Ensembl:ENSG00000196954 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:104968471..104968547 26863196 MeRIP-seq:(Medium) rs762541912 Functional Loss DEL dbSNP153 32..33 33 - - - 83778 RMVar_ID_83778 Human_SNP_ID_480213840 m1A Human chr11 - 104968473 104968473 104968473 TGACTAGGAGTTTGGGAGTAGGAACTTAGAAAACACTTGATTTATTGCTCTGAAATAAACACAAG TGACTAGGAGTTTGGGAGTAGGAACTTAGAAAGCACTTGATTTATTGCTCTGAAATAAACACAAG T C CASP4 Ensembl:ENSG00000196954 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:104968471..104968547 26863196 MeRIP-seq:(Medium) rs760952282 Functional Loss SNV dbSNP153 33..33 33 - - - 83779 RMVar_ID_83779 Human_SNP_ID_480469613 m1A Human chr11 - 106009786 106009786 106009786 TAGAGAAGGAGCGGCTGCAGATTGAAAGAGAAAAGTTGAGGTTACAGATAGTCAATTCAGAGAAA TAGAGAAGGAGCGGCTGCAGATTGAAAGAGAACAGTTGAGGTTACAGATAGTCAATTCAGAGAAA T G MSANTD4 Ensembl:ENSG00000170903 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:106009735..106009884 32194978 MeRIP-seq:(Medium) rs1394452700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23483929 RMVar_hsa_circ_152759 83780 RMVar_ID_83780 Human_SNP_ID_480472504 m1A Human chr11 - 106022164 106022164 106022164 AGGTGAGCGGTTCTATGCTGGAGGAGGCGGCCAGGGAAGCGGCGGCTCCGTGACCAGTGGGTGCC AGGTGAGCGGTTCTATGCTGGAGGAGGCGGCCGGGGAAGCGGCGGCTCCGTGACCAGTGGGTGCC T C MSANTD4 Ensembl:ENSG00000170903 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:106021887..106022215;chr11:106021923..106022209 26863196 MeRIP-seq:(Medium) rs955298644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416656 Human_Splice_Rec_1293765 83781 RMVar_ID_83781 Human_SNP_ID_480485150 m1A Human chr11 - 106077738 106077738 106077738 GGCCCAGCGCACGCCCTCCATGGATGGCACCAAGCAGAACCGTTTGGCAGGGAAAACCATACACT GGCCCAGCGCACGCCCTCCATGGATGGCACCAGGCAGAACCGTTTGGCAGGGAAAACCATACACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:106077688..106077833 26863196 MeRIP-seq:(Medium) rs748434117 Functional Loss SNV dbSNP153 33..33 33 - - - 83782 RMVar_ID_83782 Human_SNP_ID_480714408 m1A Human chr11 + 107018114 107018087 107018114 GGCGGTGGCGGCGAGGACGCGAGCGGCGGCGGAGGCGGCGGTGGCGGGACCGGCAAGCGACAACG GGCGGT___________________________GGCGGCGGTGGCGGGACCGGCAAGCGACAACG TGGCGGCGAGGACGCGAGCGGCGGCGGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:107018067..107018212 26863196 MeRIP-seq:(Medium) rs763140292 Functional Loss DEL dbSNP153 7..33 33 - - - 83783 RMVar_ID_83783 Human_SNP_ID_480714422 m1A Human chr11 + 107018114 107018105 107018114 GGCGGTGGCGGCGAGGACGCGAGCGGCGGCGGAGGCGGCGGTGGCGGGACCGGCAAGCGACAACG GGCGGTGGCGGCGAGGACGCGAGC_________GGCGGCGGTGGCGGGACCGGCAAGCGACAACG CGGCGGCGGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:107018067..107018212 26863196 MeRIP-seq:(Medium) rs1165050537 Functional Loss DEL dbSNP153 25..33 33 - - - 83784 RMVar_ID_83784 Human_SNP_ID_480714425 m1A Human chr11 - 107018123 107018108 107018123 CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCCACCGCCGCCTCCGCCGCCGCTCGCGTCCTCGCC CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCC_______________GCCGCTCGCGTCCTCGCC CGGCGGAGGCGGCGGT C GUCY1A2 Ensembl:ENSG00000152402 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:107018076..107018220 26863196 MeRIP-seq:(Medium) rs1474277534 Functional Loss DEL dbSNP153 33..47 33 - - - 83785 RMVar_ID_83785 Human_SNP_ID_480714428 m1A Human chr11 - 107018123 107018114 107018123 CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCCACCGCCGCCTCCGCCGCCGCTCGCGTCCTCGCC CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCC_________TCCGCCGCCGCTCGCGTCCTCGCC AGGCGGCGGT A GUCY1A2 Ensembl:ENSG00000152402 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:107018076..107018220 26863196 MeRIP-seq:(Medium) rs1460573963 Functional Loss DEL dbSNP153 33..41 33 - - - 83786 RMVar_ID_83786 Human_SNP_ID_480714431 m1A Human chr11 - 107018123 107018123 107018123 CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCCACCGCCGCCTCCGCCGCCGCTCGCGTCCTCGCC CGCGCTTAACGTTGTCGCTTGCCGGTCCCGCCCCCGCCGCCTCCGCCGCCGCTCGCGTCCTCGCC T G GUCY1A2 Ensembl:ENSG00000152402 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:107018076..107018220 26863196 MeRIP-seq:(Medium) rs1046943710 Functional Loss SNV dbSNP153 33..33 33 - - - 83787 RMVar_ID_83787 Human_SNP_ID_480714530 m1A Human chr11 + 107018403 107018403 107018403 CGCCGCGCTCCCGCTCACGGGGAGGCTCCGAGAGTGTGTGACCGCGGTCGGCGGGGCGGGGAGGG CGCCGCGCTCCCGCTCACGGGGAGGCTCCGAGTGTGTGTGACCGCGGTCGGCGGGGCGGGGAGGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:107018352..107018438 26863196 MeRIP-seq:(Medium) rs918695258 Functional Loss SNV dbSNP153 33..33 33 - - - 83788 RMVar_ID_83788 Human_SNP_ID_480789323 m1A Human chr11 - 107317901 107317901 107317901 AACACCTATATCGAAAAAGAAGAAAGACTGTGAACCATCTAACTTTATATCTTAGGGAACTAGAA AACACCTATATCGAAAAAGAAGAAAGACTGTGTACCATCTAACTTTATATCTTAGGGAACTAGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:107317853..107317918 26863196 MeRIP-seq:(Medium) rs1277490759 Functional Loss SNV dbSNP153 33..33 33 - - - 83789 RMVar_ID_83789 Human_SNP_ID_480817407 m1A Human chr11 - 107429349 107429349 107429349 GGGAACGGTGGAGGAAACCCACATATTCAGATAAAGCACAAAATTGTCAAGAAAGTAGAGAATCA GGGAACGGTGGAGGAAACCCACATATTCAGATGAAGCACAAAATTGTCAAGAAAGTAGAGAATCA T C CWF19L2 Ensembl:ENSG00000152404 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:107429298..107429413 26863196 MeRIP-seq:(Medium) rs745441606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2247911,Human_RBP_ID_24542590 RMVar_hsa_circ_272,RMVar_hsa_circ_61831,RMVar_hsa_circ_337231,RMVar_hsa_circ_19692,RMVar_hsa_circ_308968,RMVar_hsa_circ_365904,RMVar_hsa_circ_365599,RMVar_hsa_circ_99418,RMVar_hsa_circ_152787,RMVar_hsa_circ_152788,RMVar_hsa_circ_152789,RMVar_hsa_circ_71609,RMVar_hsa_circ_339132,RMVar_hsa_circ_366344,RMVar_hsa_circ_71495,RMVar_hsa_circ_54859,RMVar_hsa_circ_60145,RMVar_hsa_circ_324299,RMVar_hsa_circ_50685,RMVar_hsa_circ_376815,RMVar_hsa_circ_152791,RMVar_hsa_circ_352985,RMVar_hsa_circ_152792 83790 RMVar_ID_83790 Human_SNP_ID_480824669 m1A Human chr11 - 107457765 107457765 107457765 CTGCTAGTGGTAGATTTGAAAGTGCGAAGAGTATCGAAGAGCGGAAAGAACAGACCCGGAATGCC CTGCTAGTGGTAGATTTGAAAGTGCGAAGAGTGTCGAAGAGCGGAAAGAACAGACCCGGAATGCC T C CWF19L2 Ensembl:ENSG00000152404 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:107457667..107457786 26863196 MeRIP-seq:(Medium) rs770289453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520937,Human_RBP_ID_9364257,Human_RBP_ID_11511153,Human_RBP_ID_23484254,Human_RBP_ID_24364437,Human_RBP_ID_24542592,Human_RBP_ID_27803982 Human_Splice_Rec_1293899 83791 RMVar_ID_83791 Human_SNP_ID_480848146 m1A Human chr11 - 107560880 107560880 107560880 TGTTTTTTTACAGTTTGCTATGGACAGCAACCATCAAAGTAATTACAAACTCAGTAAAACTGAGA TGTTTTTTTACAGTTTGCTATGGACAGCAACCGTCAAAGTAATTACAAACTCAGTAAAACTGAGA T C ALKBH8 Ensembl:ENSG00000137760 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:107560831..107560967 26863196 MeRIP-seq:(Medium) rs958389377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1293994,Human_Splice_Rec_1294014,Human_Splice_Rec_1294032,Human_Splice_Rec_1294052,Human_Splice_Rec_1294068,Human_Splice_Rec_1294088,Human_Splice_Rec_1294102 RMVar_hsa_circ_33926,RMVar_hsa_circ_61795 83792 RMVar_ID_83792 Human_SNP_ID_480849189 m1A Human chr11 - 107565690 107565690 107565690 ATGGCCGCGCCCAGGGGAGATGGCGTGCAAGTATCCGCTGCGGTGTTCTGGTGCTAGAGTGGAGA ATGGCCGCGCCCAGGGGAGATGGCGTGCAAGTGTCCGCTGCGGTGTTCTGGTGCTAGAGTGGAGA T C ALKBH8 Ensembl:ENSG00000137760 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:107565569..107565719 26863196 MeRIP-seq:(Medium) rs533567283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4146248,Human_RBP_ID_5415559 Human_Splice_Rec_1293993,Human_Splice_Rec_1294013,Human_Splice_Rec_1294051,Human_Splice_Rec_1294067,Human_Splice_Rec_1294087,Human_Splice_Rec_1294101 83793 RMVar_ID_83793 Human_SNP_ID_480903550 m1A Human chr11 - 107792102 107792102 107792102 TTGGGTACAGATGAGGCCTTGGGGCTGACTGCATGTGGCAGAAAACGGGTGGGTCAGCCCTTGAA TTGGGTACAGATGAGGCCTTGGGGCTGACTGCGTGTGGCAGAAAACGGGTGGGTCAGCCCTTGAA T C SLC35F2 Ensembl:ENSG00000110660 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:107792053..107792119 26863196 MeRIP-seq:(Medium) rs1051376243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_388045,Human_RBP_ID_6039639,Human_RBP_ID_8176046,Human_RBP_ID_8997848,Human_RBP_ID_22490645,Human_RBP_ID_23484372,Human_RBP_ID_26409930 RMVar_hsa_circ_152808,RMVar_hsa_circ_93410 83794 RMVar_ID_83794 Human_SNP_ID_480921157 m1A Human chr11 - 107858750 107858750 107858750 CGCGCAAGGGCGCCGATGGAGGCAGACTCGCCAGCGGGCCCCGGCGCCCCAGAGCCCCTCGCGGA CGCGCAAGGGCGCCGATGGAGGCAGACTCGCCCGCGGGCCCCGGCGCCCCAGAGCCCCTCGCGGA T G SLC35F2 Ensembl:ENSG00000110660 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:107858582..107858767 26863196 MeRIP-seq:(Medium) rs373270254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184399 Human_Splice_Rec_1294195,Human_Splice_Rec_1294213,Human_Splice_Rec_1294227,Human_Splice_Rec_1294253,Human_Splice_Rec_1294265 RMVar_hsa_circ_1886,RMVar_hsa_circ_152809,RMVar_hsa_circ_333002,RMVar_hsa_circ_152818 83795 RMVar_ID_83795 Human_SNP_ID_480984701 m1A Human chr11 + 108105699 108105699 108105699 TGAGGACGTGAACAACTTGAAAGAGAAAATTGATTCCCCTTGAGGAAAGAATGGCTCAACGTGGA TGAGGACGTGAACAACTTGAAAGAGAAAATTGTTTCCCCTTGAGGAAAGAATGGCTCAACGTGGA A T CUL5 Ensembl:ENSG00000166266 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs73000543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93465,RMVar_hsa_circ_152841,RMVar_hsa_circ_108111,RMVar_hsa_circ_152856,RMVar_hsa_circ_152855 83796 RMVar_ID_83796 Human_SNP_ID_480989107 m1A Human chr11 - 108121671 108121671 108121671 TGCTGTGGGGACGAACCCCGCTCACCTGCACCAGCCTCCGGAGCAGGGGGCTGCGGCTGCGGGCG TGCTGTGGGGACGAACCCCGCTCACCTGCACCGGCCTCCGGAGCAGGGGGCTGCGGCTGCGGGCG T C AP002433.1 Ensembl:ENSG00000255467 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:108121576..108121700 32194978 MeRIP-seq:(Medium) rs1429772457 Functional Loss SNV dbSNP153 33..33 33 - - - 83797 RMVar_ID_83797 Human_SNP_ID_480991666 m1A Human chr11 + 108131910 108131910 108131910 TTATAACATTATAAATATTTATATTACAGGAAATAAGATATGTGGAACGGAGTTATGTATCAAAA TTATAACATTATAAATATTTATATTACAGGAAGTAAGATATGTGGAACGGAGTTATGTATCAAAA A G ACAT1 Ensembl:ENSG00000075239 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:108131901..108131950 26863196 MeRIP-seq:(Medium) rs1352801361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185363 Human_Splice_Rec_1294376,Human_Splice_Rec_1294377,Human_Splice_Rec_1294398,Human_Splice_Rec_1294399,Human_Splice_Rec_1294418,Human_Splice_Rec_1294419,Human_Splice_Rec_1294424,Human_Splice_Rec_1294425,Human_Splice_Rec_1294434,Human_Splice_Rec_1294435,Human_Splice_Rec_1294456,Human_Splice_Rec_1294457,Human_Splice_Rec_1294478,Human_Splice_Rec_1294479,Human_Splice_Rec_1294508,Human_Splice_Rec_1294509,Human_Splice_Rec_1294530,Human_Splice_Rec_1294531,Human_Splice_Rec_1294552,Human_Splice_Rec_1294553,Human_Splice_Rec_1294566,Human_Splice_Rec_1294567,Human_Splice_Rec_1294580,Human_Splice_Rec_1294581,Human_Splice_Rec_1294586,Human_Splice_Rec_1294587,Human_Splice_Rec_1294596,Human_Splice_Rec_1294600,Human_Splice_Rec_1294601,Human_Splice_Rec_1294622,Human_Splice_Rec_1294623 RMVar_hsa_circ_152862,RMVar_hsa_circ_334173,RMVar_hsa_circ_355286,RMVar_hsa_circ_358713,RMVar_hsa_circ_364357,RMVar_hsa_circ_335382,RMVar_hsa_circ_297234,RMVar_hsa_circ_306143,RMVar_hsa_circ_152863,RMVar_hsa_circ_152861 83798 RMVar_ID_83798 Human_SNP_ID_481092107 m1A Human chr11 + 108498382 108498382 108498382 CGCGGGAGGCGGCGCATGGTCGGCGGGGCACAACTGCGGTCCAGCTCCGCGGCGGCGAGGAGGGG CGCGGGAGGCGGCGCATGGTCGGCGGGGCACAGCTGCGGTCCAGCTCCGCGGCGGCGAGGAGGGG A G lnc-ATM-1 RNACentral:URS00008B2405 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:108498281..108498497 26863410 MeRIP-seq:(Medium) rs1249540737 Functional Loss SNV dbSNP153 33..33 33 - - - 83799 RMVar_ID_83799 Human_SNP_ID_481109960 m1A Human chr11 + 108569105 108569103 108569105 ACTCTGGTGACATTCACTACGATGGTGTCTGCATCTCCCTGTAGTCTTTCACATCTTTATGGCTT ACTCTGGTGACATTCACTACGATGGTGTCTG__TCTCCCTGTAGTCTTTCACATCTTTATGGCTT GCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:108568828..108569126 26863196 MeRIP-seq:(Medium) rs1440880282 Functional Loss DEL dbSNP153 32..33 33 - - - 83800 RMVar_ID_83800 Human_SNP_ID_481109961 m1A Human chr11 + 108569105 108569105 108569105 ACTCTGGTGACATTCACTACGATGGTGTCTGCATCTCCCTGTAGTCTTTCACATCTTTATGGCTT ACTCTGGTGACATTCACTACGATGGTGTCTGCGTCTCCCTGTAGTCTTTCACATCTTTATGGCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:108568828..108569126 26863196 MeRIP-seq:(Medium) rs1238178765 Functional Loss SNV dbSNP153 33..33 33 - - - 83801 RMVar_ID_83801 Human_SNP_ID_481133292 m1A Human chr11 - 108665137 108665119 108665138 TGGCCGTTTTGCCCATTGCGGCGGCGGCGGCGACAGCTCGGATCAACCCCAGACACGAGACACCT TGGCCGTTTTGCCCATTGCGGCGGCGGCGGC___________________AGACACGAGACACCT TGGGGTTGATCCGAGCTGTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:108665100..108665285 26863196 MeRIP-seq:(Medium) rs763385721 Functional Loss DEL dbSNP153 32..50 33 - - - 83802 RMVar_ID_83802 Human_SNP_ID_481133321 m1A Human chr11 + 108665161 108665161 108665161 CCGAGCTGTCGCCGCCGCCGCCGCAATGGGCAAAACGGCCAACTCTCCGGGTTCGGGAGCCCGAC CCGAGCTGTCGCCGCCGCCGCCGCAATGGGCAGAACGGCCAACTCTCCGGGTTCGGGAGCCCGAC A G DDX10 Ensembl:ENSG00000178105 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:108665110..108665287 26863196 MeRIP-seq:(Medium) rs1434996444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185367,Human_RBP_ID_5520963,Human_RBP_ID_9276686,Human_RBP_ID_9364272,Human_RBP_ID_18416660 83803 RMVar_ID_83803 Human_SNP_ID_481133328 m1A Human chr11 - 108665172 108665170 108665173 CACCGGGTCGGGTCGGGCTCCCGAACCCGGAGAGTTGGCCGTTTTGCCCATTGCGGCGGCGGCGG CACCGGGTCGGGTCGGGCTCCCGAACCCGGA___TTGGCCGTTTTGCCCATTGCGGCGGCGGCGG ACTC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:108665126..108665286 26863196 MeRIP-seq:(Medium) rs1382720334 Functional Loss DEL dbSNP153 32..34 33 - - - 83804 RMVar_ID_83804 Human_SNP_ID_481176642 m1A Human chr11 + 108841424 108841424 108841424 CTTACATAAAGCAAAGGAAAGACTTCAGGAAGAGGACAAATTTGACAAAGAAGAATATAGGAAAA CTTACATAAAGCAAAGGAAAGACTTCAGGAAGTGGACAAATTTGACAAAGAAGAATATAGGAAAA A T DDX10 Ensembl:ENSG00000178105 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:108841374..108841530 26863196 MeRIP-seq:(Medium) rs143913148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2249241,Human_RBP_ID_6041707,Human_RBP_ID_27804003 Human_Splice_Rec_1295537,Human_Splice_Rec_1295571,Human_Splice_Rec_1295609 RMVar_hsa_circ_52793,RMVar_hsa_circ_361652,RMVar_hsa_circ_153012,RMVar_hsa_circ_373408,RMVar_hsa_circ_87577,RMVar_hsa_circ_95251,RMVar_hsa_circ_153015,RMVar_hsa_circ_50471,RMVar_hsa_circ_153018,RMVar_hsa_circ_77867,RMVar_hsa_circ_153017,RMVar_hsa_circ_292664,RMVar_hsa_circ_353665,RMVar_hsa_circ_368924,RMVar_hsa_circ_116539,RMVar_hsa_circ_153020 83805 RMVar_ID_83805 Human_SNP_ID_481176656 m1A Human chr11 + 108841472 108841472 108841472 AGAAGAATATAGGAAAAAAATTAAGGCAAAGCATCGGGTAAGCTTTCCATCTTGAATTCATACTG AGAAGAATATAGGAAAAAAATTAAGGCAAAGCGTCGGGTAAGCTTTCCATCTTGAATTCATACTG A G DDX10 Ensembl:ENSG00000178105 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:108838525..108852200 32194978 MeRIP-seq:(Medium) rs1156858089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26319202 Human_Splice_Rec_1295537,Human_Splice_Rec_1295571,Human_Splice_Rec_1295609 RMVar_hsa_circ_52793,RMVar_hsa_circ_361652,RMVar_hsa_circ_153012,RMVar_hsa_circ_373408,RMVar_hsa_circ_87577,RMVar_hsa_circ_95251,RMVar_hsa_circ_153015,RMVar_hsa_circ_50471,RMVar_hsa_circ_153018,RMVar_hsa_circ_77867,RMVar_hsa_circ_153017,RMVar_hsa_circ_292664,RMVar_hsa_circ_353665,RMVar_hsa_circ_368924,RMVar_hsa_circ_116539,RMVar_hsa_circ_153020 83806 RMVar_ID_83806 Human_SNP_ID_481194964 m1A Human chr11 - 108917929 108917929 108917929 GGATCTGGGAGTGTGCTTGGATCAAATCCATCATCATCATCATCATCATCATCACTCCAATCCAG GGATCTGGGAGTGTGCTTGGATCAAATCCATCGTCATCATCATCATCATCATCACTCCAATCCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:108917818..108917956 26863196 MeRIP-seq:(Medium) rs759776612 Functional Loss SNV dbSNP153 33..33 33 - - - 83807 RMVar_ID_83807 Human_SNP_ID_481194965 m1A Human chr11 + 108917931 108917931 108917931 GGATTGGAGTGATGATGATGATGATGATGATGATGGATTTGATCCAAGCACACTCCCAGATCCAG GGATTGGAGTGATGATGATGATGATGATGATGGTGGATTTGATCCAAGCACACTCCCAGATCCAG A G DDX10 Ensembl:ENSG00000178105 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:108917823..108917957 26863196 MeRIP-seq:(Medium) rs946127791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17805384,Human_RBP_ID_26319205 Human_Splice_Rec_1295540,Human_Splice_Rec_1295541,Human_Splice_Rec_1295574,Human_Splice_Rec_1295575,Human_Splice_Rec_1295612,Human_Splice_Rec_1295622,Human_Splice_Rec_1295624,Human_Splice_Rec_1295625 RMVar_hsa_circ_87577,RMVar_hsa_circ_50471,RMVar_hsa_circ_153018,RMVar_hsa_circ_368924,RMVar_hsa_circ_153021,RMVar_hsa_circ_323391,RMVar_hsa_circ_319707 83808 RMVar_ID_83808 Human_SNP_ID_663057549 m1A Human chr19 + 30011208 30011208 30011208 CTGGCAGTGGCCACTCTGCCCAGGAGCTGCCGACCATCAGGACGCCTGCAGACATTTACAGGTGG CTGGCAGTGGCCACTCTGCCCAGGAGCTGCCGTCCATCAGGACGCCTGCAGACATTTACAGGTGG A T URI1 Ensembl:ENSG00000105176 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:30011101..30011250 32194978 MeRIP-seq:(Medium) rs755058946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518687,Human_RBP_ID_6737879,Human_RBP_ID_8831499,Human_RBP_ID_9294375,Human_RBP_ID_9380873,Human_RBP_ID_17919539,Human_RBP_ID_26334897 Human_Splice_Rec_1987853,Human_Splice_Rec_1987895,Human_Splice_Rec_1987913,Human_Splice_Rec_1987959 RMVar_hsa_circ_193819,RMVar_hsa_circ_287690,RMVar_hsa_circ_80027,RMVar_hsa_circ_193818,RMVar_hsa_circ_193825,RMVar_hsa_circ_278693,RMVar_hsa_circ_193826,RMVar_hsa_circ_193823,RMVar_hsa_circ_193824,RMVar_hsa_circ_356083,RMVar_hsa_circ_67468,RMVar_hsa_circ_278882,RMVar_hsa_circ_193827,RMVar_hsa_circ_193828,RMVar_hsa_circ_59159,RMVar_hsa_circ_333992 83809 RMVar_ID_83809 Human_SNP_ID_663130127 m1A Human chr19 + 30287399 30287399 30287399 GTGAATGGATGGATGCATAAATAAATGGATAAATGAATGGATGGATGGATAGATGAATAGACGGA GTGAATGGATGGATGCATAAATAAATGGATAAGTGAATGGATGGATGGATAGATGAATAGACGGA A G ZNF536 Ensembl:ENSG00000198597 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:30287396..30287509 26863196 MeRIP-seq:(Medium) rs1186209895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23790699 RMVar_hsa_circ_193831,RMVar_hsa_circ_193833,RMVar_hsa_circ_275457,RMVar_hsa_circ_318480,RMVar_hsa_circ_193832 83810 RMVar_ID_83810 Human_SNP_ID_663409530 m1A Human chr19 - 31350127 31350127 31350127 CCCCGGCCCGGGGACCACGCTGGGGGCTCCGGAGTCGGCGGGTGGAGAGGAGTGCGAGCCGGGTG CCCCGGCCCGGGGACCACGCTGGGGGCTCCGGGGTCGGCGGGTGGAGAGGAGTGCGAGCCGGGTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:31350082..31350195 26863196 MeRIP-seq:(Medium) rs1431842910 Functional Loss SNV dbSNP153 33..33 33 - - - 83811 RMVar_ID_83811 Human_SNP_ID_663672566 m1A Human chr19 + 32345682 32345682 32345682 TGAGGAGGGGGAAACCGGGGGAAAAGAGGGAAAAGAGCCGGGAGAGAGGTGGGCAAGGACGAGGG TGAGGAGGGGGAAACCGGGGGAAAAGAGGGAAGAGAGCCGGGAGAGAGGTGGGCAAGGACGAGGG A G ZNF507 Ensembl:ENSG00000168813 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:32345626..32352958 26863196 MeRIP-seq:(Medium) rs1478571999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772818,Human_RBP_ID_4516913,Human_RBP_ID_5526956,Human_RBP_ID_8233639,Human_RBP_ID_18421337 83812 RMVar_ID_83812 Human_SNP_ID_663672574 m1A Human chr19 + 32345694 32345694 32345694 AACCGGGGGAAAAGAGGGAAAAGAGCCGGGAGAGAGGTGGGCAAGGACGAGGGCGAGGGCACGGC AACCGGGGGAAAAGAGGGAAAAGAGCCGGGAGGGAGGTGGGCAAGGACGAGGGCGAGGGCACGGC A G ZNF507 Ensembl:ENSG00000168813 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:32345645..32345825 26863196 MeRIP-seq:(Medium) rs1033577703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772818,Human_RBP_ID_4516913,Human_RBP_ID_5376334,Human_RBP_ID_5526956,Human_RBP_ID_8233639,Human_RBP_ID_18421337 Human_Splice_Rec_1988845,Human_Splice_Rec_1988855,Human_Splice_Rec_1988867,Human_Splice_Rec_1988873 83813 RMVar_ID_83813 Human_SNP_ID_663687668 m1A Human chr19 - 32405830 32405813 32405830 CCGACGGGGCTAGGCGGGAACGGGGCCGCGCCACGGGCCGCAGCGCGCCGCGGGTACAAGGAGGG CCGACGGGGCTAGGCGGGAACGGGGCCGCGCC_________________GCGGGTACAAGGAGGG CGGCGCGCTGCGGCCCGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:32405791..32405909;chr19:32405780..32406094 26863196 MeRIP-seq:(Medium) rs1270254947 Functional Loss DEL dbSNP153 33..49 33 - - - 83814 RMVar_ID_83814 Human_SNP_ID_663687678 m1A Human chr19 - 32405830 32405830 32405830 CCGACGGGGCTAGGCGGGAACGGGGCCGCGCCACGGGCCGCAGCGCGCCGCGGGTACAAGGAGGG CCGACGGGGCTAGGCGGGAACGGGGCCGCGCCCCGGGCCGCAGCGCGCCGCGGGTACAAGGAGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:32405791..32405909;chr19:32405780..32406094 26863196 MeRIP-seq:(Medium) rs1378844102 Functional Loss SNV dbSNP153 33..33 33 - - - 83815 RMVar_ID_83815 Human_SNP_ID_663687679 m1A Human chr19 - 32405859 32405834 32405859 TCACGCGCGGCTCCGGGAGGGGAAGGAGGCCGACGGGGCTAGGCGGGAACGGGGCCGCGCCACGG TCACGCGCGGCTCCGGGAGGGGAAGGAGGCCG_________________________CGCCACGG GCGGCCCCGTTCCCGCCTAGCCCCGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:32405808..32406218 26863196 MeRIP-seq:(Medium) rs1309820649 Functional Loss DEL dbSNP153 33..57 33 - - - 83816 RMVar_ID_83816 Human_SNP_ID_663687806 m1A Human chr19 - 32406179 32406179 32406179 CTCCCAAGACCGCGAGCGGCCGCCGGGGTCGCAGCCCAGGCCCTGCCTCGCCGCACGGCCGACGA CTCCCAAGACCGCGAGCGGCCGCCGGGGTCGCGGCCCAGGCCCTGCCTCGCCGCACGGCCGACGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32406163..32406230 26863196 MeRIP-seq:(Medium) rs1316818916 Functional Loss SNV dbSNP153 33..33 33 - - - 83817 RMVar_ID_83817 Human_SNP_ID_663688539 m1A Human chr19 + 32408271 32408271 32408271 TGTAAGTCTGACATCATGATGTCCATCCGGCAAAGAAGAGAAATAAGAGCCACAGAAGTTTCTGA TGTAAGTCTGACATCATGATGTCCATCCGGCAGAGAAGAGAAATAAGAGCCACAGAAGTTTCTGA A G DPY19L3 Ensembl:ENSG00000178904 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:32408144..32408270 26863196 MeRIP-seq:(Medium) rs766874594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913412,Human_RBP_ID_3956691,Human_RBP_ID_4517150,Human_RBP_ID_9380880,Human_RBP_ID_18997400,Human_RBP_ID_23791616 Human_Splice_Rec_1988894,Human_Splice_Rec_1988895,Human_Splice_Rec_1988898,Human_Splice_Rec_1988899,Human_Splice_Rec_1988904,Human_Splice_Rec_1988905,Human_Splice_Rec_1988940,Human_Splice_Rec_1988941,Human_Splice_Rec_1988978,Human_Splice_Rec_1988979,Human_Splice_Rec_1989014,Human_Splice_Rec_1989015 RMVar_hsa_circ_22940,RMVar_hsa_circ_117874,RMVar_hsa_circ_282965,RMVar_hsa_circ_193851,RMVar_hsa_circ_121877,RMVar_hsa_circ_193852,RMVar_hsa_circ_193853 83818 RMVar_ID_83818 Human_SNP_ID_663733728 m1A Human chr19 + 32581281 32581281 32581281 CTGACGCCGAGCCATGGCGGACGAGGAGCTTGAGGCGCTGAGGAGACAGAGGCTGGCCGAGCTGC CTGACGCCGAGCCATGGCGGACGAGGAGCTTGGGGCGCTGAGGAGACAGAGGCTGGCCGAGCTGC A G PDCD5 Ensembl:ENSG00000105185 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:32581116..32581370;chr19:32581108..32581366;chr19:32581116..32581377;chr19:32581116..32581619 26863196 MeRIP-seq:(Medium) rs1344025213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519049,Human_RBP_ID_825966,Human_RBP_ID_1188513,Human_RBP_ID_1559321,Human_RBP_ID_4558327,Human_RBP_ID_6740488,Human_RBP_ID_8482848,Human_RBP_ID_8831851,Human_RBP_ID_9329964,Human_RBP_ID_9380885,Human_RBP_ID_13425710,Human_RBP_ID_18727500,Human_RBP_ID_22502229,Human_RBP_ID_23130992,Human_RBP_ID_23211238,Human_RBP_ID_26987932 Human_Splice_Rec_1989101,Human_Splice_Rec_1989111,Human_Splice_Rec_1989117,Human_Splice_Rec_1989127,Human_Splice_Rec_1989135 RMVar_hsa_circ_76035,RMVar_hsa_circ_95095,RMVar_hsa_circ_193864,RMVar_hsa_circ_193865 83819 RMVar_ID_83819 Human_SNP_ID_663733749 m1A Human chr19 - 32581329 32581329 32581329 GAGGGCCAAGCCTGGCGGGGGCTGATGCGCTCACCCCGTGTTTGGCCTGCAGCTCGGCCAGCCTC GAGGGCCAAGCCTGGCGGGGGCTGATGCGCTCCCCCCGTGTTTGGCCTGCAGCTCGGCCAGCCTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:32581263..32581560 32194978 MeRIP-seq:(Medium) rs1040271604 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 83820 RMVar_ID_83820 Human_SNP_ID_663733825 m1A Human chr19 - 32581479 32581456 32581479 GGGCCCCTCGCGACGAGGAAAGCGACGAGGCCACCTCTGAGCCGGCCACGAGGCCGCCAGGGCAG GGGCCCCTCGCGACGAGGAAAGCGACGAGGCC_______________________GCCAGGGCAG CGGCCTCGTGGCCGGCTCAGAGGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:32581476..32581583 26863196 MeRIP-seq:(Medium) rs1004109428 Functional Loss DEL dbSNP153 33..55 33 - - - 83821 RMVar_ID_83821 Human_SNP_ID_663733827 m1A Human chr19 - 32581461 32581461 32581461 AAAGCGACGAGGCCACCTCTGAGCCGGCCACGAGGCCGCCAGGGCAGCGCAGGGGACCGGGGCCC AAAGCGACGAGGCCACCTCTGAGCCGGCCACGTGGCCGCCAGGGCAGCGCAGGGGACCGGGGCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32581455..32581629 26863196 MeRIP-seq:(Medium) rs1414925800 Functional Loss SNV dbSNP153 33..33 33 - - - 83822 RMVar_ID_83822 Human_SNP_ID_663733836 m1A Human chr19 - 32581479 32581479 32581479 GGGCCCCTCGCGACGAGGAAAGCGACGAGGCCACCTCTGAGCCGGCCACGAGGCCGCCAGGGCAG GGGCCCCTCGCGACGAGGAAAGCGACGAGGCCTCCTCTGAGCCGGCCACGAGGCCGCCAGGGCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:32581476..32581583 26863196 MeRIP-seq:(Medium) rs1048758220 Functional Loss SNV dbSNP153 33..33 33 - - - 83823 RMVar_ID_83823 Human_SNP_ID_663734074 m1A Human chr19 + 32582179 32582175 32582180 CCGCCTCCCGTGAAATTTCTCTATTAAATTTAAGTTTTTTTTTTCCAGGATCCTGGTGATGCGGC CCGCCTCCCGTGAAATTTCTCTATTAAAT_____TTTTTTTTTTCCAGGATCCTGGTGATGCGGC TTTAAG T PDCD5 Ensembl:ENSG00000105185 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:32582176..32582250 26863196 MeRIP-seq:(Medium) rs771737633 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_25399237 Human_Splice_Rec_1989103,Human_Splice_Rec_1989113,Human_Splice_Rec_1989119,Human_Splice_Rec_1989129,Human_Splice_Rec_1989137,Human_Splice_Rec_1989141 RMVar_hsa_circ_76035,RMVar_hsa_circ_95095,RMVar_hsa_circ_193864,RMVar_hsa_circ_193865 83824 RMVar_ID_83824 Human_SNP_ID_663734078 m1A Human chr19 + 32582178 32582178 32582178 GCCGCCTCCCGTGAAATTTCTCTATTAAATTTAAGTTTTTTTTTTCCAGGATCCTGGTGATGCGG GCCGCCTCCCGTGAAATTTCTCTATTAAATTTGAGTTTTTTTTTTCCAGGATCCTGGTGATGCGG A G PDCD5 Ensembl:ENSG00000105185 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:32582176..32582250;chr19:32582176..32582200 26863196 MeRIP-seq:(Medium) rs947903250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25399237 Human_Splice_Rec_1989103,Human_Splice_Rec_1989113,Human_Splice_Rec_1989119,Human_Splice_Rec_1989129,Human_Splice_Rec_1989137,Human_Splice_Rec_1989141 RMVar_hsa_circ_76035,RMVar_hsa_circ_95095,RMVar_hsa_circ_193864,RMVar_hsa_circ_193865 83825 RMVar_ID_83825 Human_SNP_ID_663734079 m1A Human chr19 + 32582179 32582179 32582179 CCGCCTCCCGTGAAATTTCTCTATTAAATTTAAGTTTTTTTTTTCCAGGATCCTGGTGATGCGGC CCGCCTCCCGTGAAATTTCTCTATTAAATTTACGTTTTTTTTTTCCAGGATCCTGGTGATGCGGC A C PDCD5 Ensembl:ENSG00000105185 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:32582176..32582250 26863196 MeRIP-seq:(Medium) rs1176378062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25399237 Human_Splice_Rec_1989103,Human_Splice_Rec_1989113,Human_Splice_Rec_1989119,Human_Splice_Rec_1989129,Human_Splice_Rec_1989137,Human_Splice_Rec_1989141 RMVar_hsa_circ_76035,RMVar_hsa_circ_95095,RMVar_hsa_circ_193864,RMVar_hsa_circ_193865 83826 RMVar_ID_83826 Human_SNP_ID_663734810 m1A Human chr19 + 32584956 32584956 32584956 GTGTTTGACCTATGTTTTCGTTGTAGGGAAGCAGAAATGAGAAACAGTATCTTAGCCCAAGTTCT GTGTTTGACCTATGTTTTCGTTGTAGGGAAGCGGAAATGAGAAACAGTATCTTAGCCCAAGTTCT A G PDCD5 Ensembl:ENSG00000105185 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32584951..32584975 26863196 MeRIP-seq:(Medium) rs750678059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769579,Human_RBP_ID_1559357,Human_RBP_ID_1883437,Human_RBP_ID_4517289,Human_RBP_ID_6740563,Human_RBP_ID_13425882,Human_RBP_ID_22545895,Human_RBP_ID_27272308,Human_RBP_ID_27816364 Human_Splice_Rec_1989104,Human_Splice_Rec_1989105,Human_Splice_Rec_1989114,Human_Splice_Rec_1989115,Human_Splice_Rec_1989120,Human_Splice_Rec_1989121,Human_Splice_Rec_1989130,Human_Splice_Rec_1989131,Human_Splice_Rec_1989142,Human_Splice_Rec_1989143,Human_Splice_Rec_1989149 Human_miRNA_ID_2648638,Human_miRNA_ID_2671234,Human_miRNA_ID_3101885 RMVar_hsa_circ_2497,RMVar_hsa_circ_76035,RMVar_hsa_circ_97698,RMVar_hsa_circ_193864,RMVar_hsa_circ_89835,RMVar_hsa_circ_193866,RMVar_hsa_circ_193867 83827 RMVar_ID_83827 Human_SNP_ID_663760307 m1A Human chr19 + 32674547 32674547 32674547 ATCTCTCGGTGCTTAAGAGTTTTCCTTTAACAATCTTTACCTGTGGGAATGCAGAGACCCCCCCG ATCTCTCGGTGCTTAAGAGTTTTCCTTTAACAGTCTTTACCTGTGGGAATGCAGAGACCCCCCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:32674536..32674799 26863196 MeRIP-seq:(Medium) rs1277666201 Functional Loss SNV dbSNP153 33..33 33 - - - 83828 RMVar_ID_83828 Human_SNP_ID_663760522 m1A Human chr19 - 32675127 32675127 32675127 GGTGGTGGGCATCGAGGTCCCAGCAGCGGACGAGGGAGGTGCCGCCGTCGCCCAGGATGGGCTGG GGTGGTGGGCATCGAGGTCCCAGCAGCGGACGGGGGAGGTGCCGCCGTCGCCCAGGATGGGCTGG T C ANKRD27 Ensembl:ENSG00000105186 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:32675016..32675149;chr19:32675035..32675149 26863196 MeRIP-seq:(Medium) rs1368397826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4517413,Human_RBP_ID_18421339 Human_Splice_Rec_1989157,Human_Splice_Rec_1989231,Human_Splice_Rec_1989257,Human_Splice_Rec_1989269,Human_Splice_Rec_1989283 RMVar_hsa_circ_91625,RMVar_hsa_circ_193910,RMVar_hsa_circ_105519,RMVar_hsa_circ_193932,RMVar_hsa_circ_81924,RMVar_hsa_circ_193942 83829 RMVar_ID_83829 Human_SNP_ID_663760527 m1A Human chr19 - 32675130 32675130 32675130 GAGGGTGGTGGGCATCGAGGTCCCAGCAGCGGACGAGGGAGGTGCCGCCGTCGCCCAGGATGGGC GAGGGTGGTGGGCATCGAGGTCCCAGCAGCGGGCGAGGGAGGTGCCGCCGTCGCCCAGGATGGGC T C ANKRD27 Ensembl:ENSG00000105186 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:32675069..32675155 26863196 MeRIP-seq:(Medium) rs543330636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558333,Human_RBP_ID_18421339 Human_Splice_Rec_1989157,Human_Splice_Rec_1989231,Human_Splice_Rec_1989257,Human_Splice_Rec_1989269,Human_Splice_Rec_1989283 RMVar_hsa_circ_91625,RMVar_hsa_circ_193910,RMVar_hsa_circ_105519,RMVar_hsa_circ_193932,RMVar_hsa_circ_81924,RMVar_hsa_circ_193942 83830 RMVar_ID_83830 Human_SNP_ID_663765140 m1A Human chr19 - 32691890 32691890 32691890 AGCTCCACGGCAGGTGGCCCGGCCCTGCAGGGACCCCAGCACCTCCGGGGGCCTCGCGGGAATTG AGCTCCACGGCAGGTGGCCCGGCCCTGCAGGGCCCCCAGCACCTCCGGGGGCCTCGCGGGAATTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:32691851..32692001 26863196 MeRIP-seq:(Medium) rs1048338948 Functional Loss SNV dbSNP153 33..33 33 - - - 83831 RMVar_ID_83831 Human_SNP_ID_663765155 m1A Human chr19 - 32691916 32691916 32691916 CCCGGATCCGATTCTGGCGCGGCCTGAGCTCCACGGCAGGTGGCCCGGCCCTGCAGGGACCCCAG CCCGGATCCGATTCTGGCGCGGCCTGAGCTCCGCGGCAGGTGGCCCGGCCCTGCAGGGACCCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:32691866..32691996 26863196 MeRIP-seq:(Medium) rs1245209640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27466753 83832 RMVar_ID_83832 Human_SNP_ID_663765400 m1A Human chr19 - 32692262 32692262 32692262 TCTTGTGGTCATCGGTGTCGGGCAGCGACGGGAAAGCGGTGCGGCTGAATGGCGCCGGGCCCAGG TCTTGTGGTCATCGGTGTCGGGCAGCGACGGGCAAGCGGTGCGGCTGAATGGCGCCGGGCCCAGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32691840..32692325 26863196 MeRIP-seq:(Medium) rs781040551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6740797 83833 RMVar_ID_83833 Human_SNP_ID_663765619 m1A Human chr19 + 32692490 32692490 32692490 CTGGCGCGACCGCGTGCGCCAGGACCCGCGCCACTTCCTGCGGCTGTGCGCCCACCTCGACTGCA CTGGCGCGACCGCGTGCGCCAGGACCCGCGCCGCTTCCTGCGGCTGTGCGCCCACCTCGACTGCA A G NUDT19 Ensembl:ENSG00000213965 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:32692326..32692500 26863196 MeRIP-seq:(Medium) rs1309657182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558334,Human_RBP_ID_8482936,Human_RBP_ID_8831905,Human_RBP_ID_27466757 83834 RMVar_ID_83834 Human_SNP_ID_663826987 m1A Human chr19 + 32928459 32928459 32928459 ATGCTTCTGAGGCTTGTTTTTTCACCCTGGTCATGGTAGGTCTGTAGTAACCTTTCCTAAAAAGC ATGCTTCTGAGGCTTGTTTTTTCACCCTGGTCGTGGTAGGTCTGTAGTAACCTTTCCTAAAAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32928306..32928520 26863196 MeRIP-seq:(Medium) rs1473855673 Functional Loss SNV dbSNP153 33..33 33 - - - 83835 RMVar_ID_83835 Human_SNP_ID_663829761 m1A Human chr19 - 32940403 32940403 32940403 GAGGAGTGTTGGAAGGAGAGGAGGAGCCCGGCATGGGAAGATGTGTAGAGCGTGATGGGGAGGAG GAGGAGTGTTGGAAGGAGAGGAGGAGCCCGGCCTGGGAAGATGTGTAGAGCGTGATGGGGAGGAG T G CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32940356..32940511 26863196 MeRIP-seq:(Medium) rs1568571374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85219,RMVar_hsa_circ_128097,RMVar_hsa_circ_193957,RMVar_hsa_circ_193956,RMVar_hsa_circ_266203,RMVar_hsa_circ_97923,RMVar_hsa_circ_193976,RMVar_hsa_circ_30355,RMVar_hsa_circ_345891,RMVar_hsa_circ_362838,RMVar_hsa_circ_66502,RMVar_hsa_circ_193978,RMVar_hsa_circ_337959,RMVar_hsa_circ_299591,RMVar_hsa_circ_21345,RMVar_hsa_circ_94804,RMVar_hsa_circ_193985,RMVar_hsa_circ_193986,RMVar_hsa_circ_326449,RMVar_hsa_circ_77872,RMVar_hsa_circ_193987,RMVar_hsa_circ_193988 83836 RMVar_ID_83836 Human_SNP_ID_663834871 m1A Human chr19 + 32959974 32959974 32959974 CTGTCCTGTTCAACACTGCTCACATCACTCTCAGACCGGGACCTCTGGCGAGGCTGAGGAATAGC CTGTCCTGTTCAACACTGCTCACATCACTCTCGGACCGGGACCTCTGGCGAGGCTGAGGAATAGC A G lnc-GPATCH1-2 RNACentral:URS00009BE8A7 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:32959923..32960024 32194978 MeRIP-seq:(Medium) rs1265905657 Functional Loss SNV dbSNP153 33..33 33 - - - 83837 RMVar_ID_83837 Human_SNP_ID_663837113 m1A Human chr19 - 32969113 32969113 32969113 TCCGCTGAAAGCTACAGAGACCACCTGCCAGCAGAGAGGAGCTACACTCTGCTGCGAGCTTCAGA TCCGCTGAAAGCTACAGAGACCACCTGCCAGCGGAGAGGAGCTACACTCTGCTGCGAGCTTCAGA T C CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:32969065..32969366 32194978 MeRIP-seq:(Medium) rs1352057653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85219,RMVar_hsa_circ_193956,RMVar_hsa_circ_97923,RMVar_hsa_circ_193976,RMVar_hsa_circ_101142,RMVar_hsa_circ_126929,RMVar_hsa_circ_193989,RMVar_hsa_circ_193990 83838 RMVar_ID_83838 Human_SNP_ID_663837167 m1A Human chr19 + 32969320 32969320 32969320 CCCAGGGTTTTTATGGACCTCAGCGGGGAAGAAGTGTGTGCTGATTGGGCCATTGGCAGGCCCAG CCCAGGGTTTTTATGGACCTCAGCGGGGAAGAGGTGTGTGCTGATTGGGCCATTGGCAGGCCCAG A G lnc-GPATCH1-2 RNACentral:URS00009BE8A7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:32969272..32969371 26863196 MeRIP-seq:(Medium) rs933075557 Functional Loss SNV dbSNP153 33..33 33 - - - 83839 RMVar_ID_83839 Human_SNP_ID_663837385 m1A Human chr19 - 32970165 32970165 32970165 CTGGAGAGTTGGCCTGGGCCTGGCAGGGAGTAAGGAAAGAATTCTGGGTGCAGAAGACAGCAAAT CTGGAGAGTTGGCCTGGGCCTGGCAGGGAGTAGGGAAAGAATTCTGGGTGCAGAAGACAGCAAAT T C CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:32970063..32970164 32194978 MeRIP-seq:(Medium) rs566424846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4517688,Human_RBP_ID_6741232,Human_RBP_ID_13427246 RMVar_hsa_circ_85219,RMVar_hsa_circ_193956,RMVar_hsa_circ_97923,RMVar_hsa_circ_193976,RMVar_hsa_circ_101142,RMVar_hsa_circ_126929,RMVar_hsa_circ_193989,RMVar_hsa_circ_193990 83840 RMVar_ID_83840 Human_SNP_ID_663837477 m1A Human chr19 - 32970564 32970564 32970564 TAAACCCGAGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGCGACA TAAACCCGAGAGGCAGAGGTTGCAGTGAGCCAGGATTGTGCCACTGCACTCCAGCCTGGGCGACA T C CEP89 Ensembl:ENSG00000121289 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1035834329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85219,RMVar_hsa_circ_193956,RMVar_hsa_circ_97923,RMVar_hsa_circ_193976,RMVar_hsa_circ_101142,RMVar_hsa_circ_126929,RMVar_hsa_circ_193989,RMVar_hsa_circ_193990 83841 RMVar_ID_83841 Human_SNP_ID_663845253 m1A Human chr19 - 33000603 33000603 33000603 TGTGCAGGCCCGCAGAGGGGTGCAGGCCGGGCATGACAGGGTCTGGGCTATGCCAGGAGGTTCTG TGTGCAGGCCCGCAGAGGGGTGCAGGCCGGGCGTGACAGGGTCTGGGCTATGCCAGGAGGTTCTG T C RHPN2 Ensembl:ENSG00000131941 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33000557..33000745 26863196 MeRIP-seq:(Medium) rs1469142006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39358,RMVar_hsa_circ_92468,RMVar_hsa_circ_376314,RMVar_hsa_circ_193994,RMVar_hsa_circ_193995,RMVar_hsa_circ_369946,RMVar_hsa_circ_79432,RMVar_hsa_circ_193999,RMVar_hsa_circ_194000,RMVar_hsa_circ_359062 83842 RMVar_ID_83842 Human_SNP_ID_663859772 m1A Human chr19 - 33059210 33059210 33059210 GAAGGTGAGCTGGGGATGGGGCCCAGGAGTCGAGGCGGGGGGTGAAGATTGCCAACAGCTGCTGC GAAGGTGAGCTGGGGATGGGGCCCAGGAGTCGGGGCGGGGGGTGAAGATTGCCAACAGCTGCTGC T C RHPN2 Ensembl:ENSG00000131941 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33059189..33059254 26863196 MeRIP-seq:(Medium) rs1046093314 Functional Loss SNV dbSNP153 33..33 33 - - - 83843 RMVar_ID_83843 Human_SNP_ID_663865623 m1A Human chr19 - 33081258 33081258 33081258 TCCGCCGGCCCACGCGGCCCGCACCTTCTTCCAGAGGCTCCAGCCCGGTCCCATAGCTGACCAGA TCCGCCGGCCCACGCGGCCCGCACCTTCTTCCTGAGGCTCCAGCCCGGTCCCATAGCTGACCAGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33081207..33081788 26863196 MeRIP-seq:(Medium) rs1253546752 Functional Loss SNV dbSNP153 33..33 33 - - - 83844 RMVar_ID_83844 Human_SNP_ID_663865713 m1A Human chr19 + 33081611 33081611 33081611 GCTCAGACTTGAAACCGAGGAAGAAAACAACCATGAGCAAATCTGGAGGGAAAGCATTTCAGGCA GCTCAGACTTGAAACCGAGGAAGAAAACAACCCTGAGCAAATCTGGAGGGAAAGCATTTCAGGCA A C GPATCH1 Ensembl:ENSG00000076650 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:33081608..33081744 26863196 MeRIP-seq:(Medium) rs200533332 Functional Loss SNV dbSNP153 33..33 33 - - - 83845 RMVar_ID_83845 Human_SNP_ID_663887936 m1A Human chr19 - 33167740 33167737 33167740 AGAGGAGAGAGGAGGAGAGGAGAGAAGAGAAAAGAGGAGGGAAGGCAGGAAGGAAGGATTGAAGG AGAGGAGAGAGGAGGAGAGGAGAGAAGAGAAA___GGAGGGAAGGCAGGAAGGAAGGATTGAAGG CTCT C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33167689..33167887 26863196 MeRIP-seq:(Medium) rs1028664361 Functional Loss DEL dbSNP153 33..35 33 - - - 83846 RMVar_ID_83846 Human_SNP_ID_663888989 m1A Human chr19 - 33172244 33172243 33172244 AATCAAAAGACATGGGCTGTCAAGGCACAAAAAGACAGAGGAACCTTCAATGCACATTGTTATGC AATCAAAAGACATGGGCTGTCAAGGCACAAAA_GACAGAGGAACCTTCAATGCACATTGTTATGC CT C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33172164..33172247 26863196 MeRIP-seq:(Medium) rs1319187670 Functional Loss DEL dbSNP153 33..33 33 - - - 83847 RMVar_ID_83847 Human_SNP_ID_663895010 m1A Human chr19 + 33194635 33194635 33194635 CGCACAAAGACGCCTCGGGAGCCGCCGCCTGCACCCGGGCCGCAGCAGCCACGCCAGCCGGAGCC CGCACAAAGACGCCTCGGGAGCCGCCGCCTGCCCCCGGGCCGCAGCAGCCACGCCAGCCGGAGCC A C LRP3 Ensembl:ENSG00000130881 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:33194536..33194648 26863410 MeRIP-seq:(Medium) rs1464926183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557405 83848 RMVar_ID_83848 Human_SNP_ID_663895051 m1A Human chr19 + 33194700 33194700 33194700 CGAGCCCTAGCCCGAGCCCGAGCCCGAGCCGCAGCCAGAGCCAGAGCCGGAGCCGCAGCCGGAAC CGAGCCCTAGCCCGAGCCCGAGCCCGAGCCGCCGCCAGAGCCAGAGCCGGAGCCGCAGCCGGAAC A C LRP3 Ensembl:ENSG00000130881 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33194523..33194883 26863196 MeRIP-seq:(Medium) rs1425457407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557405 83849 RMVar_ID_83849 Human_SNP_ID_663897781 m1A Human chr19 - 33204726 33204726 33204726 GGCAGGTGGGATGGCGGAGCCACAGAGGCGGAAGGCCTCCTGGCGGGGTGGGGCTGCTGGGCCCA GGCAGGTGGGATGGCGGAGCCACAGAGGCGGAGGGCCTCCTGGCGGGGTGGGGCTGCTGGGCCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:33204628..33204779 32194978 MeRIP-seq:(Medium) rs1427699098 Functional Loss SNV dbSNP153 33..33 33 - - - 83850 RMVar_ID_83850 Human_SNP_ID_663897786 m1A Human chr19 - 33204733 33204733 33204733 AGATGAAGGCAGGTGGGATGGCGGAGCCACAGAGGCGGAAGGCCTCCTGGCGGGGTGGGGCTGCT AGATGAAGGCAGGTGGGATGGCGGAGCCACAGCGGCGGAAGGCCTCCTGGCGGGGTGGGGCTGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33204683..33204794 26863196 MeRIP-seq:(Medium) rs1432397374 Functional Loss SNV dbSNP153 33..33 33 - - - 83851 RMVar_ID_83851 Human_SNP_ID_663898027 m1A Human chr19 - 33205343 33205343 33205343 GCCGAGCAGTTGCCCTCATCAGAGCCGTCTCCACACTCGTCCACCGTGTTGCACTGCCACGGGCC GCCGAGCAGTTGCCCTCATCAGAGCCGTCTCCGCACTCGTCCACCGTGTTGCACTGCCACGGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:33205294..33205398 26863196 MeRIP-seq:(Medium) rs1256370062 Functional Loss SNV dbSNP153 33..33 33 - - - 83852 RMVar_ID_83852 Human_SNP_ID_663898933 m1A Human chr19 + 33207119 33207119 33207119 AACCGGCTCTTTCACCGGCCGCGGGCGCCCCGAGGCCAGATCCCACTGCTGACCGCAGCACGCCC AACCGGCTCTTTCACCGGCCGCGGGCGCCCCGGGGCCAGATCCCACTGCTGACCGCAGCACGCCC A G LRP3 Ensembl:ENSG00000130881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:33207068..33207209 26863196 MeRIP-seq:(Medium) rs1466507992 Functional Loss SNV dbSNP153 33..33 33 - - - 83853 RMVar_ID_83853 Human_SNP_ID_663898936 m1A Human chr19 + 33207124 33207124 33207124 GCTCTTTCACCGGCCGCGGGCGCCCCGAGGCCAGATCCCACTGCTGACCGCAGCACGCCCCTCAC GCTCTTTCACCGGCCGCGGGCGCCCCGAGGCCCGATCCCACTGCTGACCGCAGCACGCCCCTCAC A C LRP3 Ensembl:ENSG00000130881 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33207074..33207234 26863196 MeRIP-seq:(Medium) rs1242093376 Functional Loss SNV dbSNP153 33..33 33 - - - 83854 RMVar_ID_83854 Human_SNP_ID_663925985 m1A Human chr19 - 33301763 33301763 33301763 AGTTCCAGATCGCGCACTGCGGCCAGACCACCATGCACCTGCAGCCCGGTCACCCCACGCCGCCG AGTTCCAGATCGCGCACTGCGGCCAGACCACCGTGCACCTGCAGCCCGGTCACCCCACGCCGCCG T C CEBPA Ensembl:ENSG00000245848 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33301615..33301986 26863196 MeRIP-seq:(Medium) rs1378898437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27466845 83855 RMVar_ID_83855 Human_SNP_ID_663926109 m1A Human chr19 - 33302023 33302023 33302023 GCCCGGGGGAGCGCACGGGCCCCCGCCCGGCTACGGCTGCGCGGCCGCCGGCTACCTGGACGGCA GCCCGGGGGAGCGCACGGGCCCCCGCCCGGCTTCGGCTGCGCGGCCGCCGGCTACCTGGACGGCA T A CEBPA Ensembl:ENSG00000245848 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:33301984..33302095 26863196 MeRIP-seq:(Medium) rs1300977671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772573,Human_RBP_ID_912247,Human_RBP_ID_4565826,Human_RBP_ID_17502746,Human_RBP_ID_27466847 Clinvar_Rec_435 83856 RMVar_ID_83856 Human_SNP_ID_663926225 m1A Human chr19 + 33302277 33302277 33302277 TCGCAGATGCCGCCCAGCGGCTCCGGGGCGGCAGGTGGGGCGGGAGGCTGCGCGGGGCCCGCGCC TCGCAGATGCCGCCCAGCGGCTCCGGGGCGGCGGGTGGGGCGGGAGGCTGCGCGGGGCCCGCGCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:33302226..33302450 26863196 MeRIP-seq:(Medium) rs1387400759 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_436 83857 RMVar_ID_83857 Human_SNP_ID_663926226 m1A Human chr19 + 33302277 33302277 33302277 TCGCAGATGCCGCCCAGCGGCTCCGGGGCGGCAGGTGGGGCGGGAGGCTGCGCGGGGCCCGCGCC TCGCAGATGCCGCCCAGCGGCTCCGGGGCGGCTGGTGGGGCGGGAGGCTGCGCGGGGCCCGCGCC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:33302226..33302450 26863196 MeRIP-seq:(Medium) rs1387400759 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_436 83858 RMVar_ID_83858 Human_SNP_ID_663926275 m1A Human chr19 + 33302359 33302359 33302359 CGGCGCTGCTGGGCGCGTGCGGGGGGCTCTGCAGGTGGCTGCTCATCGGGGGCCGCGGCTCCGCC CGGCGCTGCTGGGCGCGTGCGGGGGGCTCTGCTGGTGGCTGCTCATCGGGGGCCGCGGCTCCGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33302113..33302492 26863196 MeRIP-seq:(Medium) rs1315626965 Functional Loss SNV dbSNP153 33..33 33 - - - 83859 RMVar_ID_83859 Human_SNP_ID_663943850 m1A Human chr19 - 33373799 33373799 33373799 CGAGCCGACCCAGGCCTCACAGCCCGCGAGTCAGCGAGGAGGAGCGACGGTTACGAAACCGGCAG CGAGCCGACCCAGGCCTCACAGCCCGCGAGTCGGCGAGGAGGAGCGACGGTTACGAAACCGGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33373748..33373947 26863196 MeRIP-seq:(Medium) rs916279754 Functional Loss SNV dbSNP153 33..33 33 - - - 83860 RMVar_ID_83860 Human_SNP_ID_663943851 m1A Human chr19 - 33373799 33373799 33373799 CGAGCCGACCCAGGCCTCACAGCCCGCGAGTCAGCGAGGAGGAGCGACGGTTACGAAACCGGCAG CGAGCCGACCCAGGCCTCACAGCCCGCGAGTCCGCGAGGAGGAGCGACGGTTACGAAACCGGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33373748..33373947 26863196 MeRIP-seq:(Medium) rs916279754 Functional Loss SNV dbSNP153 33..33 33 - - - 83861 RMVar_ID_83861 Human_SNP_ID_663943880 m1A Human chr19 - 33373870 33373870 33373870 TCCTTACCTGCTCCTCTAGCCCGCCTGCCCCCAGGCGGCCTCCACTCCGAGCGGCCCCGCGCGGT TCCTTACCTGCTCCTCTAGCCCGCCTGCCCCCGGGCGGCCTCCACTCCGAGCGGCCCCGCGCGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:33373729..33373925 26863410 MeRIP-seq:(Medium) rs1053771227 Functional Loss SNV dbSNP153 33..33 33 - - - 83862 RMVar_ID_83862 Human_SNP_ID_663949662 m1A Human chr19 - 33394862 33394862 33394862 GGGCAGGTGCAGGGGTGCTTCGGGAAAGCCAGAATGAGGTTTGGTGCTTGCTGGGGGTTGGGGCA GGGCAGGTGCAGGGGTGCTTCGGGAAAGCCAGCATGAGGTTTGGTGCTTGCTGGGGGTTGGGGCA T G PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33394856..33394983 26863196 MeRIP-seq:(Medium) rs1344974470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83041,RMVar_hsa_circ_114883,RMVar_hsa_circ_194021,RMVar_hsa_circ_194022 83863 RMVar_ID_83863 Human_SNP_ID_663954904 m1A Human chr19 + 33413582 33413582 33413582 AGGGGAGCCAGGGTGCCCCGCTTACCTGCCGCAGATGCAGGTGTAGGAGCTGTGGCGCATGCCGC AGGGGAGCCAGGGTGCCCCGCTTACCTGCCGCGGATGCAGGTGTAGGAGCTGTGGCGCATGCCGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:33411676..33462952 32194978 MeRIP-seq:(Medium) rs1455265714 Functional Loss SNV dbSNP153 33..33 33 - - - 83864 RMVar_ID_83864 Human_SNP_ID_663957200 m1A Human chr19 - 33422358 33422358 33422358 GATGGGTAGATGGATGATAAGTAGGTAGATATAGGCAGATGATTGATTGATTGATTGATGGGATA GATGGGTAGATGGATGATAAGTAGGTAGATATGGGCAGATGATTGATTGATTGATTGATGGGATA T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33422355..33423101 26863196 MeRIP-seq:(Medium) rs1487910063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114883,RMVar_hsa_circ_194022 83865 RMVar_ID_83865 Human_SNP_ID_663960200 m1A Human chr19 - 33434138 33434138 33434138 CAGGGACACGAACAGCGCTGAAAGTGATGTCTAGCAAAAGAAGCCAGGCTCAGAAAGGCACGTAC CAGGGACACGAACAGCGCTGAAAGTGATGTCTGGCAAAAGAAGCCAGGCTCAGAAAGGCACGTAC T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33434134..33434217 26863196 MeRIP-seq:(Medium) rs985708987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13428124 RMVar_hsa_circ_114883,RMVar_hsa_circ_194022 83866 RMVar_ID_83866 Human_SNP_ID_663961742 m1A Human chr19 - 33440330 33440330 33440330 GCAGGCCCTGGGTAGGTTGTGAAGGCAGAGCCAGCAGGACTCAGCAGCCCATCAGGGCTGGGTGT GCAGGCCCTGGGTAGGTTGTGAAGGCAGAGCCGGCAGGACTCAGCAGCCCATCAGGGCTGGGTGT T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33440315..33440676 26863196 MeRIP-seq:(Medium) rs1252200767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26785578 RMVar_hsa_circ_114883,RMVar_hsa_circ_194022 83867 RMVar_ID_83867 Human_SNP_ID_663965925 m1A Human chr19 + 33456917 33456917 33456917 GCATCTCCAGGACCTCCCGGAGGAAGACGGGGACCTCCTAGTGACTTCCCTCTCCAGTGAAACCT GCATCTCCAGGACCTCCCGGAGGAAGACGGGGCCCTCCTAGTGACTTCCCTCTCCAGTGAAACCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33456911..33457035 26863196 MeRIP-seq:(Medium) rs1345335922 Functional Loss SNV dbSNP153 33..33 33 - - - 83868 RMVar_ID_83868 Human_SNP_ID_663969305 m1A Human chr19 - 33469535 33469535 33469535 AGGACAGATGGGGAGTCCTGGGAGTTTGGAGGAGGAGAGGTGAGAGTGGACCCATCTGCTGGCTG AGGACAGATGGGGAGTCCTGGGAGTTTGGAGGGGGAGAGGTGAGAGTGGACCCATCTGCTGGCTG T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:33469495..33469645 26863196 MeRIP-seq:(Medium) rs552214227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114883,RMVar_hsa_circ_194022,RMVar_hsa_circ_194024,RMVar_hsa_circ_353639,RMVar_hsa_circ_374786,RMVar_hsa_circ_194025,RMVar_hsa_circ_373394 83869 RMVar_ID_83869 Human_SNP_ID_663969330 m1A Human chr19 + 33469641 33469641 33469641 GCTCACACGCCCACCTGGGGATCCCAGCTCCAACCTCCACCAGCTCCTGCTAGAAGCTCCATGGC GCTCACACGCCCACCTGGGGATCCCAGCTCCACCCTCCACCAGCTCCTGCTAGAAGCTCCATGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33469628..33469833 26863196 MeRIP-seq:(Medium) rs1352957228 Functional Loss SNV dbSNP153 33..33 33 - - - 83870 RMVar_ID_83870 Human_SNP_ID_663969427 m1A Human chr19 - 33470043 33470043 33470043 TAGGATGACGCCCGGGTCTCTGCTGAAGCAGCAGGAAGATGGCAGAGCCTCATTGAGATGGGGGC TAGGATGACGCCCGGGTCTCTGCTGAAGCAGCGGGAAGATGGCAGAGCCTCATTGAGATGGGGGC T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33470040..33470167 26863196 MeRIP-seq:(Medium) rs1447629126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114883,RMVar_hsa_circ_194022,RMVar_hsa_circ_194024,RMVar_hsa_circ_353639,RMVar_hsa_circ_374786,RMVar_hsa_circ_194025,RMVar_hsa_circ_373394 83871 RMVar_ID_83871 Human_SNP_ID_663974507 m1A Human chr19 - 33490045 33490045 33490045 TCTGTGTTCTCTCTCCCCAGCGTGGCGTCAACACGGACAGCGGCAGTGTCTGCAGGGAGGCCTCC TCTGTGTTCTCTCTCCCCAGCGTGGCGTCAACGCGGACAGCGGCAGTGTCTGCAGGGAGGCCTCC T C PEPD Ensembl:ENSG00000124299 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:33489976..33490075 32194978 MeRIP-seq:(Medium) rs757112748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4518518,Human_RBP_ID_23792293 Human_Splice_Rec_1990100,Human_Splice_Rec_1990101,Human_Splice_Rec_1990128,Human_Splice_Rec_1990129,Human_Splice_Rec_1990164,Human_Splice_Rec_1990165,Human_Splice_Rec_1990184,Human_Splice_Rec_1990185,Human_Splice_Rec_1990212,Human_Splice_Rec_1990213,Human_Splice_Rec_1990250,Human_Splice_Rec_1990251,Human_Splice_Rec_1990284,Human_Splice_Rec_1990285,Human_Splice_Rec_1990292,Human_Splice_Rec_1990293,Human_Splice_Rec_1990304,Human_Splice_Rec_1990305 RMVar_hsa_circ_194024,RMVar_hsa_circ_353639,RMVar_hsa_circ_374786,RMVar_hsa_circ_194025,RMVar_hsa_circ_373394,RMVar_hsa_circ_359445 83872 RMVar_ID_83872 Human_SNP_ID_663978618 m1A Human chr19 + 33505699 33505699 33505699 ACAACACACCCTCATCACAAACACCCTACACAACACACACACCTGCACACAACACGGCACACTCA ACAACACACCCTCATCACAAACACCCTACACACCACACACACCTGCACACAACACGGCACACTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33505649..33505754 26863196 MeRIP-seq:(Medium) rs1462975514 Functional Loss SNV dbSNP153 33..33 33 - - - 83873 RMVar_ID_83873 Human_SNP_ID_664053928 m1A Human chr19 + 33795676 33795676 33795676 GAGGAGGAGGAGGCACGGGCGGGGCGCAAAGGAAACAGGAGGAAGAGGAAGGGGAGGAGGAGTGG GAGGAGGAGGAGGCACGGGCGGGGCGCAAAGGTAACAGGAGGAAGAGGAAGGGGAGGAGGAGTGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:33795625..33795722 26863196 MeRIP-seq:(Medium) rs1448576022 Functional Loss SNV dbSNP153 33..33 33 - - - 83874 RMVar_ID_83874 Human_SNP_ID_664053936 m1A Human chr19 - 33795706 33795701 33795707 CGGCCGCCCCTTCCTCCTTTTCTCCCACTCCCACTCCTCCTCCCCTTCCTCTTCCTCCTGTTTCC CGGCCGCCCCTTCCTCCTTTTCTCCCACTCC______TCCTCCCCTTCCTCTTCCTCCTGTTTCC AGGAGTG A lnc-PEPD-4,lnc-PEPD-4:2 RNACentral:URS0000D59B8B,RNACentral:URS0000D58BD5 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33795611..33795764 26863196 MeRIP-seq:(Medium) rs1462524396 Functional Loss DEL dbSNP153 32..37 33 - - - 83875 RMVar_ID_83875 Human_SNP_ID_664054779 m1A Human chr19 + 33797618 33797618 33797618 CCTGCAGATCCGGTTCCCCGCTGCCCGCCCGCACCCCCTGACCTGGACGCGCGCACCCGGCACAC CCTGCAGATCCGGTTCCCCGCTGCCCGCCCGCGCCCCCTGACCTGGACGCGCGCACCCGGCACAC A G KCTD15 Ensembl:ENSG00000153885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:33797614..33797710;chr19:33797608..33797771 26863196 MeRIP-seq:(Medium) rs987147565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583526,Human_RBP_ID_3954840,Human_RBP_ID_5650076,Human_RBP_ID_8728401,Human_RBP_ID_18490622 RMVar_hsa_circ_194029,RMVar_hsa_circ_85565 83876 RMVar_ID_83876 Human_SNP_ID_664054780 m1A Human chr19 + 33797618 33797618 33797618 CCTGCAGATCCGGTTCCCCGCTGCCCGCCCGCACCCCCTGACCTGGACGCGCGCACCCGGCACAC CCTGCAGATCCGGTTCCCCGCTGCCCGCCCGCTCCCCCTGACCTGGACGCGCGCACCCGGCACAC A T KCTD15 Ensembl:ENSG00000153885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:33797614..33797710;chr19:33797608..33797771 26863196 MeRIP-seq:(Medium) rs987147565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583526,Human_RBP_ID_3954840,Human_RBP_ID_5650076,Human_RBP_ID_8728401,Human_RBP_ID_18490622 RMVar_hsa_circ_194029,RMVar_hsa_circ_85565 83877 RMVar_ID_83877 Human_SNP_ID_664055651 m1A Human chr19 - 33800488 33800487 33800488 CGCGGTGCCGGTGCTGCCGTGTGTGTGAAGCGAGGACCCGCTCGGCCGCTCCTTGCGGTGAGGCA CGCGGTGCCGGTGCTGCCGTGTGTGTGAAGCG_GGACCCGCTCGGCCGCTCCTTGCGGTGAGGCA CT C lnc-PEPD-2 RNACentral:URS00008B8CDA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33800370..33800563 26863196 MeRIP-seq:(Medium) rs768656764 Functional Loss DEL dbSNP153 33..33 33 - - - 83878 RMVar_ID_83878 Human_SNP_ID_664058638 m1A Human chr19 - 33811539 33811539 33811539 GGCAGCGTGCAGCCCTCACCTGTACCGAGTTGAGCCGGCAGTAGCCATTGAGCGGGAAGCGGATG GGCAGCGTGCAGCCCTCACCTGTACCGAGTTGGGCCGGCAGTAGCCATTGAGCGGGAAGCGGATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:33811488..33811645 26863196 MeRIP-seq:(Medium) rs1046191598 Functional Loss SNV dbSNP153 33..33 33 - - - 83879 RMVar_ID_83879 Human_SNP_ID_664059093 m1A Human chr19 + 33812890 33812890 33812890 CCAGTTCAGCGAGTATGTGCTTTGCCGGGAGGAGCGGCGGCCGCAGCCCACCCCCACTGCTGTTC CCAGTTCAGCGAGTATGTGCTTTGCCGGGAGGGGCGGCGGCCGCAGCCCACCCCCACTGCTGTTC A G KCTD15 Ensembl:ENSG00000153885 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33812842..33812919 26863196 MeRIP-seq:(Medium) rs977621155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526961,Human_RBP_ID_23792390 Human_miRNA_ID_2874207,Human_miRNA_ID_2982168 RMVar_hsa_circ_194029,RMVar_hsa_circ_85565 83880 RMVar_ID_83880 Human_SNP_ID_664059392 m1A Human chr19 + 33813566 33813566 33813566 GATGCAGGGATGTGTGCTGCAGGGCTGCTGGGAGGAGAGTGGTGGGGGCCTGAGGGCTGAGTGAT GATGCAGGGATGTGTGCTGCAGGGCTGCTGGGGGGAGAGTGGTGGGGGCCTGAGGGCTGAGTGAT A G KCTD15 Ensembl:ENSG00000153885 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33813517..33813624 26863196 MeRIP-seq:(Medium) rs1058374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4518708,Human_RBP_ID_6742347,Human_RBP_ID_8832126,Human_RBP_ID_17920692,Human_RBP_ID_23792391 RMVar_hsa_circ_194029,RMVar_hsa_circ_85565 83881 RMVar_ID_83881 Human_SNP_ID_664059398 m1A Human chr19 - 33813576 33813576 33813576 TGGTTACAGAATCACTCAGCCCTCAGGCCCCCACCACTCTCCTCCCAGCAGCCCTGCAGCACACA TGGTTACAGAATCACTCAGCCCTCAGGCCCCCGCCACTCTCCTCCCAGCAGCCCTGCAGCACACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:33813527..33813626 26863196 MeRIP-seq:(Medium) rs1046242140 Functional Loss SNV dbSNP153 33..33 33 - - - 83882 RMVar_ID_83882 Human_SNP_ID_664150429 m1A Human chr19 - 34172607 34172605 34172607 GCCGCCGCCGCCGCTCCCAGCTGCTCGCAGAGAGGCAGATCCCACGCCACTGTCGCCCGCTCCGC GCCGCCGCCGCCGCTCCCAGCTGCTCGCAGAG__GCAGATCCCACGCCACTGTCGCCCGCTCCGC CCT C lnc-SCGB2B2-4 RNACentral:URS00008BEEDB lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:34172526..34172675 26863196 MeRIP-seq:(Medium) rs1262476119 Functional Loss DEL dbSNP153 33..34 33 - - - 83883 RMVar_ID_83883 Human_SNP_ID_664150430 m1A Human chr19 - 34172607 34172607 34172607 GCCGCCGCCGCCGCTCCCAGCTGCTCGCAGAGAGGCAGATCCCACGCCACTGTCGCCCGCTCCGC GCCGCCGCCGCCGCTCCCAGCTGCTCGCAGAGGGGCAGATCCCACGCCACTGTCGCCCGCTCCGC T C lnc-SCGB2B2-4 RNACentral:URS00008BEEDB lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:34172526..34172675 26863196 MeRIP-seq:(Medium) rs1243188117 Functional Loss SNV dbSNP153 33..33 33 - - - 83884 RMVar_ID_83884 Human_SNP_ID_664150437 m1A Human chr19 + 34172618 34172618 34172618 GACAGTGGCGTGGGATCTGCCTCTCTGCGAGCAGCTGGGAGCGGCGGCGGCGGCGCCATGAGCGG GACAGTGGCGTGGGATCTGCCTCTCTGCGAGCTGCTGGGAGCGGCGGCGGCGGCGCCATGAGCGG A T LSM14A Ensembl:ENSG00000257103 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:34172518..34172631 26863410 MeRIP-seq:(Medium) rs773970764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519419,Human_RBP_ID_4518925,Human_RBP_ID_6742493,Human_RBP_ID_8832166,Human_RBP_ID_9328882,Human_RBP_ID_9382390,Human_RBP_ID_18420907,Human_RBP_ID_22071137 RMVar_hsa_circ_194031,RMVar_hsa_circ_103512 83885 RMVar_ID_83885 Human_SNP_ID_664153682 m1A Human chr19 + 34185368 34185368 34185368 GGGTGTTAAGTTCGTAGTGGGTTCAGGAAGAGATGGTGGAGGCTGAGGGACAGATGTTTTCATTC GGGTGTTAAGTTCGTAGTGGGTTCAGGAAGAGGTGGTGGAGGCTGAGGGACAGATGTTTTCATTC A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34185366..34185455 26863196 MeRIP-seq:(Medium) rs1362858481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825272,Human_RBP_ID_6742686,Human_RBP_ID_9930845,Human_RBP_ID_25401147 RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_194032 83886 RMVar_ID_83886 Human_SNP_ID_664163207 m1A Human chr19 - 34221672 34221672 34221672 CGACCTCCTCTGAATCCACCGCGAAATCCTCGAGGGGCAGTGAAGGTACCACCTCTGCCACCACC CGACCTCCTCTGAATCCACCGCGAAATCCTCGGGGGGCAGTGAAGGTACCACCTCTGCCACCACC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:34221593..34221714 26863196 MeRIP-seq:(Medium) rs138875917 Functional Loss SNV dbSNP153 33..33 33 - - - 83887 RMVar_ID_83887 Human_SNP_ID_664164726 m1A Human chr19 + 34227830 34227802 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTG____________________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1218677556 Functional Loss DEL dbSNP153 6..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83888 RMVar_ID_83888 Human_SNP_ID_664164727 m1A Human chr19 + 34227830 34227804 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTG__________________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1351496284 Functional Loss DEL dbSNP153 8..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83889 RMVar_ID_83889 Human_SNP_ID_664164729 m1A Human chr19 + 34227830 34227808 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTG______________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs985955306 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83890 RMVar_ID_83890 Human_SNP_ID_664164730 m1A Human chr19 + 34227830 34227810 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTG____________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1378159300 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83891 RMVar_ID_83891 Human_SNP_ID_664164731 m1A Human chr19 + 34227830 34227812 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTG__________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs910283422 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83892 RMVar_ID_83892 Human_SNP_ID_664164732 m1A Human chr19 + 34227830 34227814 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTG________________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1313229898 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83893 RMVar_ID_83893 Human_SNP_ID_664164733 m1A Human chr19 + 34227830 34227816 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTG______________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs966161652 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83894 RMVar_ID_83894 Human_SNP_ID_664164734 m1A Human chr19 + 34227830 34227818 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTG____________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1174954741 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83895 RMVar_ID_83895 Human_SNP_ID_664164737 m1A Human chr19 + 34227830 34227820 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTG__________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1229338462 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83896 RMVar_ID_83896 Human_SNP_ID_664164740 m1A Human chr19 + 34227830 34227822 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTG________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1438954605 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83897 RMVar_ID_83897 Human_SNP_ID_664164742 m1A Human chr19 + 34227830 34227824 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTG______TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755853924 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83898 RMVar_ID_83898 Human_SNP_ID_664164748 m1A Human chr19 + 34227830 34227826 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTG____TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs61483260 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83899 RMVar_ID_83899 Human_SNP_ID_664164754 m1A Human chr19 + 34227830 34227828 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG__TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1491413946 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83900 RMVar_ID_83900 Human_SNP_ID_664164756 m1A Human chr19 + 34227830 34227830 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG A G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs74404860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 83901 RMVar_ID_83901 Human_SNP_ID_664172031 m1A Human chr19 + 34255013 34255013 34255013 TGGCGCCAGGACCCGCTCCCGGAAGCCCGCGGAGGGAGGGCGGCCTGCTGGCGGCAGGGGTCCGC TGGCGCCAGGACCCGCTCCCGGAAGCCCGCGGTGGGAGGGCGGCCTGCTGGCGGCAGGGGTCCGC A T KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:34254591..34255332 26863196 MeRIP-seq:(Medium) rs1048924810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581132,Human_RBP_ID_8196390 83902 RMVar_ID_83902 Human_SNP_ID_664173879 m1A Human chr19 + 34261655 34261655 34261655 ACAGCAAGAGGGGAGGACTCTTGGGCAGGGGCATGACACGTCCAAAGGTGTGGAGGTGAGAGCAA ACAGCAAGAGGGGAGGACTCTTGGGCAGGGGCGTGACACGTCCAAAGGTGTGGAGGTGAGAGCAA A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34261649..34261730 26863196 MeRIP-seq:(Medium) rs145145907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6743813 83903 RMVar_ID_83903 Human_SNP_ID_664173880 m1A Human chr19 + 34261655 34261655 34261655 ACAGCAAGAGGGGAGGACTCTTGGGCAGGGGCATGACACGTCCAAAGGTGTGGAGGTGAGAGCAA ACAGCAAGAGGGGAGGACTCTTGGGCAGGGGCTTGACACGTCCAAAGGTGTGGAGGTGAGAGCAA A T KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34261649..34261730 26863196 MeRIP-seq:(Medium) rs145145907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6743813 83904 RMVar_ID_83904 Human_SNP_ID_664176506 m1A Human chr19 + 34271995 34271995 34271995 AAGCTGAGTAGTGCAAGGGTAAGGAGGAAATGAGAAACATTTAGGATATAATAATAATAGGTAAC AAGCTGAGTAGTGCAAGGGTAAGGAGGAAATGGGAAACATTTAGGATATAATAATAATAGGTAAC A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34271988..34272110 26863196 MeRIP-seq:(Medium) rs1267009761 Functional Loss SNV dbSNP153 33..33 33 - - - 83905 RMVar_ID_83905 Human_SNP_ID_664176887 m1A Human chr19 + 34273767 34273767 34273767 TCAAAGTGGTTTCTCAGAAGAAGTGATGCCTAAGTTAGACATCCAAGAGGAATGAGAGTGAGCCA TCAAAGTGGTTTCTCAGAAGAAGTGATGCCTAGGTTAGACATCCAAGAGGAATGAGAGTGAGCCA A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:34273763..34273929 26863196 MeRIP-seq:(Medium) rs752351751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6743900 83906 RMVar_ID_83906 Human_SNP_ID_664177617 m1A Human chr19 - 34277068 34277066 34277068 GCCTCTATCCAGAAAGCTCCTGCCTCCCTCCTACTCATGATGCTCCTCCCGTTCATCCTTTAGCT GCCTCTATCCAGAAAGCTCCTGCCTCCCTCCT__TCATGATGCTCCTCCCGTTCATCCTTTAGCT AGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34277062..34277162 26863196 MeRIP-seq:(Medium) rs147729181 Functional Loss DEL dbSNP153 33..34 33 - - - 83907 RMVar_ID_83907 Human_SNP_ID_664183527 m1A Human chr19 + 34299772 34299769 34299772 GGGCCAGCCCAGTCTGGAAGCATCTCTTATTAATGTTACAAGGAAACCGCTACCTCAGCAAACAA GGGCCAGCCCAGTCTGGAAGCATCTCTTAT___TGTTACAAGGAAACCGCTACCTCAGCAAACAA TTAA T KIAA0355 Ensembl:ENSG00000166398 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34299722..34299788 26863196 MeRIP-seq:(Medium) rs1324012588 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5526963,Human_RBP_ID_17271814,Human_RBP_ID_17920966,Human_RBP_ID_27677186 Human_Splice_Rec_1990554,Human_Splice_Rec_1990560,Human_Splice_Rec_1990586,Human_Splice_Rec_1990590,Human_Splice_Rec_1990598,Human_Splice_Rec_1990602 RMVar_hsa_circ_194052,RMVar_hsa_circ_344249,RMVar_hsa_circ_366010 83908 RMVar_ID_83908 Human_SNP_ID_664183529 m1A Human chr19 + 34299772 34299772 34299772 GGGCCAGCCCAGTCTGGAAGCATCTCTTATTAATGTTACAAGGAAACCGCTACCTCAGCAAACAA GGGCCAGCCCAGTCTGGAAGCATCTCTTATTAGTGTTACAAGGAAACCGCTACCTCAGCAAACAA A G KIAA0355 Ensembl:ENSG00000166398 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34299722..34299788 26863196 MeRIP-seq:(Medium) rs970709860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526963,Human_RBP_ID_17271814,Human_RBP_ID_17920966,Human_RBP_ID_27677186 Human_Splice_Rec_1990554,Human_Splice_Rec_1990560,Human_Splice_Rec_1990586,Human_Splice_Rec_1990590,Human_Splice_Rec_1990598,Human_Splice_Rec_1990602 RMVar_hsa_circ_194052,RMVar_hsa_circ_344249,RMVar_hsa_circ_366010 83909 RMVar_ID_83909 Human_SNP_ID_664196341 m1A Human chr19 - 34349718 34349718 34349718 CTTCGAGTGCCTGGGAGCCCTGCGTGCCCTCTACTCCTGCCCATGGTCCTTAGTCTGCCACCCTG CTTCGAGTGCCTGGGAGCCCTGCGTGCCCTCTGCTCCTGCCCATGGTCCTTAGTCTGCCACCCTG T C AC010504.1 Ensembl:ENSG00000267219 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34349711..34349848 26863196 MeRIP-seq:(Medium) rs1316915077 Functional Loss SNV dbSNP153 33..33 33 - - - 83910 RMVar_ID_83910 Human_SNP_ID_664197155 m1A Human chr19 + 34352707 34352707 34352707 AAGCACCCTGGCAGCACCCTTCCCCGCTTCCCAGCACGCTGCCCAGCCCCAGCGCACCACTCTAT AAGCACCCTGGCAGCACCCTTCCCCGCTTCCCTGCACGCTGCCCAGCCCCAGCGCACCACTCTAT A T KIAA0355 Ensembl:ENSG00000166398 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:34352657..34352804;chr19:34352624..34352859 26863196 MeRIP-seq:(Medium) rs574884474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1990584,Human_Splice_Rec_1990596,Human_Splice_Rec_1990606 Human_miRNA_ID_2686201 RMVar_hsa_circ_112029,RMVar_hsa_circ_194067 83911 RMVar_ID_83911 Human_SNP_ID_664200612 m1A Human chr19 + 34365246 34365246 34365246 GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCAGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCTGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC A T GPI Ensembl:ENSG00000105220 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:34365226..34365250 26863196 MeRIP-seq:(Medium) rs1393746378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1293368,Human_RBP_ID_4557424,Human_RBP_ID_5442970,Human_RBP_ID_8483647,Human_RBP_ID_8832271,Human_RBP_ID_17267923,Human_RBP_ID_17386767,Human_RBP_ID_18192165,Human_RBP_ID_18728291,Human_RBP_ID_22447645,Human_RBP_ID_22533378,Human_RBP_ID_26467227,Human_RBP_ID_26988232,Human_RBP_ID_27272616 RMVar_hsa_circ_76576,RMVar_hsa_circ_86454,RMVar_hsa_circ_119814,RMVar_hsa_circ_194069,RMVar_hsa_circ_194070,RMVar_hsa_circ_194071 83912 RMVar_ID_83912 Human_SNP_ID_664200613 m1A Human chr19 + 34365246 34365246 34365246 GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCAGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCCGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:34365226..34365250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1293368,Human_RBP_ID_4557424,Human_RBP_ID_5442970,Human_RBP_ID_8483647,Human_RBP_ID_8832271,Human_RBP_ID_17267923,Human_RBP_ID_17386767,Human_RBP_ID_18192165,Human_RBP_ID_18728291,Human_RBP_ID_22447645,Human_RBP_ID_22533378,Human_RBP_ID_26467227,Human_RBP_ID_26988232,Human_RBP_ID_27272616 RMVar_hsa_circ_76576,RMVar_hsa_circ_86454,RMVar_hsa_circ_119814,RMVar_hsa_circ_194069,RMVar_hsa_circ_194070,RMVar_hsa_circ_194071 83913 RMVar_ID_83913 Human_SNP_ID_664200614 m1A Human chr19 + 34365246 34365246 34365246 GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCAGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC GCGCTCCTTCCTCCTCGGCTCGCGTCTCACTCGGTGTACCTTCTAGTCCCGCCATGGCCGCTCTC A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:34365226..34365250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1293368,Human_RBP_ID_4557424,Human_RBP_ID_5442970,Human_RBP_ID_8483647,Human_RBP_ID_8832271,Human_RBP_ID_17267923,Human_RBP_ID_17386767,Human_RBP_ID_18192165,Human_RBP_ID_18728291,Human_RBP_ID_22447645,Human_RBP_ID_22533378,Human_RBP_ID_26467227,Human_RBP_ID_26988232,Human_RBP_ID_27272616 RMVar_hsa_circ_76576,RMVar_hsa_circ_86454,RMVar_hsa_circ_119814,RMVar_hsa_circ_194069,RMVar_hsa_circ_194070,RMVar_hsa_circ_194071 83914 RMVar_ID_83914 Human_SNP_ID_664200632 m1A Human chr19 - 34365275 34365275 34365275 TGCAGCTTCTGGAACTGGGGGTCCCGGGTGAGAGCGGCCATGGCGGGACTAGAAGGTACACTGAG TGCAGCTTCTGGAACTGGGGGTCCCGGGTGAGGGCGGCCATGGCGGGACTAGAAGGTACACTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:34365176..34365400;chr19:34365176..34365375 26863196 MeRIP-seq:(Medium) rs762697901 Functional Loss SNV dbSNP153 33..33 33 - - - 83915 RMVar_ID_83915 Human_SNP_ID_664201777 m1A Human chr19 + 34368662 34368662 34368662 CATCCTGGTAGACGGCAAGGATGTGATGCCAGAGGTCAACAAGGTTCTGGACAAGATGAAGTCTT CATCCTGGTAGACGGCAAGGATGTGATGCCAGGGGTCAACAAGGTTCTGGACAAGATGAAGTCTT A G GPI Ensembl:ENSG00000105220 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs760550832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53148,Human_RBP_ID_1014815,Human_RBP_ID_1560177,Human_RBP_ID_1883983,Human_RBP_ID_3568224,Human_RBP_ID_3956731,Human_RBP_ID_4566108,Human_RBP_ID_5585589,Human_RBP_ID_8483658,Human_RBP_ID_13431527,Human_RBP_ID_17498974,Human_RBP_ID_18192173,Human_RBP_ID_18728306,Human_RBP_ID_18997438,Human_RBP_ID_22446637,Human_RBP_ID_22533379 Human_Splice_Rec_1990626,Human_Splice_Rec_1990636,Human_Splice_Rec_1990646,Human_Splice_Rec_1990654,Human_Splice_Rec_1990655,Human_Splice_Rec_1990690,Human_Splice_Rec_1990691,Human_Splice_Rec_1990724,Human_Splice_Rec_1990725,Human_Splice_Rec_1990736,Human_Splice_Rec_1990744,Human_Splice_Rec_1990745,Human_Splice_Rec_1990756,Human_Splice_Rec_1990757,Human_Splice_Rec_1990772,Human_Splice_Rec_1990773,Human_Splice_Rec_1990782,Human_Splice_Rec_1990783,Human_Splice_Rec_1990816,Human_Splice_Rec_1990817,Human_Splice_Rec_1990848,Human_Splice_Rec_1990849,Human_Splice_Rec_1990878,Human_Splice_Rec_1990879 RMVar_hsa_circ_76576,RMVar_hsa_circ_86454,RMVar_hsa_circ_119814,RMVar_hsa_circ_194069,RMVar_hsa_circ_194072,RMVar_hsa_circ_194070,RMVar_hsa_circ_194071,RMVar_hsa_circ_308218,RMVar_hsa_circ_319235,RMVar_hsa_circ_348972,RMVar_hsa_circ_371428,RMVar_hsa_circ_117285,RMVar_hsa_circ_79762,RMVar_hsa_circ_98226,RMVar_hsa_circ_78645,RMVar_hsa_circ_194074,RMVar_hsa_circ_194076,RMVar_hsa_circ_194077,RMVar_hsa_circ_194078,RMVar_hsa_circ_194075,RMVar_hsa_circ_108733,RMVar_hsa_circ_88571,RMVar_hsa_circ_194079,RMVar_hsa_circ_194080,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_194082,RMVar_hsa_circ_194083 83916 RMVar_ID_83916 Human_SNP_ID_664204216 m1A Human chr19 - 34377570 34377570 34377570 GCAGTTTTCTCCTCACCAGGTCGGAGCCGCCAATGCCAATGTTGATGACGTCCGTGATGGTCTTG GCAGTTTTCTCCTCACCAGGTCGGAGCCGCCAGTGCCAATGTTGATGACGTCCGTGATGGTCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34377455..34377636 26863196 MeRIP-seq:(Medium) rs1318491793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194084 83917 RMVar_ID_83917 Human_SNP_ID_664204313 m1A Human chr19 + 34377820 34377820 34377820 CGTCTGGTATGTCTCCAACATTGATGGAACTCACATTGCCAAAACCCTGGCCCAGCTGAACCCCG CGTCTGGTATGTCTCCAACATTGATGGAACTCGCATTGCCAAAACCCTGGCCCAGCTGAACCCCG A G GPI Ensembl:ENSG00000105220 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:34377770..34377942 26863196 MeRIP-seq:(Medium) rs758281551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519571,Human_RBP_ID_1188701,Human_RBP_ID_1560187,Human_RBP_ID_1883997,Human_RBP_ID_3568233,Human_RBP_ID_4519311,Human_RBP_ID_8483680,Human_RBP_ID_8832277,Human_RBP_ID_13431689,Human_RBP_ID_17267929,Human_RBP_ID_17386769,Human_RBP_ID_17498976,Human_RBP_ID_22448598,Human_RBP_ID_22533380,Human_RBP_ID_22969794,Human_RBP_ID_26467235,Human_RBP_ID_27473442 Human_Splice_Rec_1990658,Human_Splice_Rec_1990659,Human_Splice_Rec_1990692,Human_Splice_Rec_1990693,Human_Splice_Rec_1990728,Human_Splice_Rec_1990758,Human_Splice_Rec_1990766,Human_Splice_Rec_1990786,Human_Splice_Rec_1990787,Human_Splice_Rec_1990820,Human_Splice_Rec_1990821,Human_Splice_Rec_1990852,Human_Splice_Rec_1990853,Human_Splice_Rec_1990882,Human_Splice_Rec_1990883 Human_miRNA_ID_2133024,Human_miRNA_ID_2133025,Human_miRNA_ID_2663606,Human_miRNA_ID_2663607,Human_miRNA_ID_2682062,Human_miRNA_ID_2682063 RMVar_hsa_circ_76576,RMVar_hsa_circ_119814,RMVar_hsa_circ_194072,RMVar_hsa_circ_194070,RMVar_hsa_circ_194071,RMVar_hsa_circ_308218,RMVar_hsa_circ_348972,RMVar_hsa_circ_371428,RMVar_hsa_circ_117285,RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_98226,RMVar_hsa_circ_78645,RMVar_hsa_circ_194076,RMVar_hsa_circ_194077,RMVar_hsa_circ_194078,RMVar_hsa_circ_194075,RMVar_hsa_circ_88571,RMVar_hsa_circ_194080,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_194087,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_194083,RMVar_hsa_circ_372336,RMVar_hsa_circ_372500,RMVar_hsa_circ_372003,RMVar_hsa_circ_124060,RMVar_hsa_circ_294352,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_194085,RMVar_hsa_circ_194086,RMVar_hsa_circ_81935,RMVar_hsa_circ_194092,RMVar_hsa_circ_46951,RMVar_hsa_circ_194091 83918 RMVar_ID_83918 Human_SNP_ID_664204334 m1A Human chr19 - 34377883 34377883 34377883 GGGCCAGGGGCCGGGCAGTTTTCGGCACTCATACCTTGGAGGCAATGATGAACAGGGAGGACTCG GGGCCAGGGGCCGGGCAGTTTTCGGCACTCATGCCTTGGAGGCAATGATGAACAGGGAGGACTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34377691..34379057 26863196 MeRIP-seq:(Medium) rs879182695 Functional Loss SNV dbSNP153 33..33 33 - - - 83919 RMVar_ID_83919 Human_SNP_ID_664205396 m1A Human chr19 + 34381479 34381479 34381479 TTTGTTTTTTTTTTTGTAGACCAAAGTGAAGGAGTTTGGAATTGACCCTCAAAACATGTTCGAGT TTTGTTTTTTTTTTTGTAGACCAAAGTGAAGGCGTTTGGAATTGACCCTCAAAACATGTTCGAGT A C GPI Ensembl:ENSG00000105220 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1475031143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_913437,Human_RBP_ID_1560216,Human_RBP_ID_1884002,Human_RBP_ID_6744260,Human_RBP_ID_8832278,Human_RBP_ID_17271817,Human_RBP_ID_18728337,Human_RBP_ID_18997443,Human_RBP_ID_22810423,Human_RBP_ID_23792729 Human_Splice_Rec_1990664,Human_Splice_Rec_1990665,Human_Splice_Rec_1990698,Human_Splice_Rec_1990699,Human_Splice_Rec_1990792,Human_Splice_Rec_1990793,Human_Splice_Rec_1990826,Human_Splice_Rec_1990858,Human_Splice_Rec_1990859,Human_Splice_Rec_1990890,Human_Splice_Rec_1990891 RMVar_hsa_circ_119814,RMVar_hsa_circ_194072,RMVar_hsa_circ_194070,RMVar_hsa_circ_308218,RMVar_hsa_circ_371428,RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194077,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_194087,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_372336,RMVar_hsa_circ_372003,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_81935,RMVar_hsa_circ_80452,RMVar_hsa_circ_194092,RMVar_hsa_circ_46951,RMVar_hsa_circ_194091,RMVar_hsa_circ_102405,RMVar_hsa_circ_194094,RMVar_hsa_circ_194093 83920 RMVar_ID_83920 Human_SNP_ID_664205413 m1A Human chr19 + 34381518 34381518 34381518 AATTGACCCTCAAAACATGTTCGAGTTCTGGGATGTAAGTACAAGCACTTCTGCACTGGGTGAAT AATTGACCCTCAAAACATGTTCGAGTTCTGGGGTGTAAGTACAAGCACTTCTGCACTGGGTGAAT A G GPI Ensembl:ENSG00000105220 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr19:34381501..34381525;chr19:34381476..34381525;chr19:34379852..34392227 26863196,32194978 MeRIP-seq:(Medium) rs747547577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1560218,Human_RBP_ID_1884002,Human_RBP_ID_2563381,Human_RBP_ID_6744261,Human_RBP_ID_9086499,Human_RBP_ID_13431831,Human_RBP_ID_17386770,Human_RBP_ID_18997443,Human_RBP_ID_19089902,Human_RBP_ID_22446640 Human_Splice_Rec_1990664,Human_Splice_Rec_1990665,Human_Splice_Rec_1990698,Human_Splice_Rec_1990699,Human_Splice_Rec_1990792,Human_Splice_Rec_1990793,Human_Splice_Rec_1990826,Human_Splice_Rec_1990827,Human_Splice_Rec_1990858,Human_Splice_Rec_1990859,Human_Splice_Rec_1990890,Human_Splice_Rec_1990891 RMVar_hsa_circ_119814,RMVar_hsa_circ_194072,RMVar_hsa_circ_194070,RMVar_hsa_circ_308218,RMVar_hsa_circ_371428,RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194077,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_194087,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_372336,RMVar_hsa_circ_372003,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_81935,RMVar_hsa_circ_80452,RMVar_hsa_circ_194092,RMVar_hsa_circ_46951,RMVar_hsa_circ_194091,RMVar_hsa_circ_102405,RMVar_hsa_circ_194094,RMVar_hsa_circ_194093 83921 RMVar_ID_83921 Human_SNP_ID_664205498 m1A Human chr19 + 34381900 34381900 34381900 ATCTGTAAAGGCCAAGGGCAGGGTGAGGCATGAGGTATGACCGGGTAGGCCTGGAAAGGAGCAAC ATCTGTAAAGGCCAAGGGCAGGGTGAGGCATGCGGTATGACCGGGTAGGCCTGGAAAGGAGCAAC A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34381897..34381988 26863196 MeRIP-seq:(Medium) rs1357285099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6744265,Human_RBP_ID_13431854,Human_RBP_ID_22810426 RMVar_hsa_circ_119814,RMVar_hsa_circ_194070,RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_372336,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_194092,RMVar_hsa_circ_46951,RMVar_hsa_circ_102405,RMVar_hsa_circ_194093,RMVar_hsa_circ_194096 83922 RMVar_ID_83922 Human_SNP_ID_664205737 m1A Human chr19 - 34382914 34382914 34382914 TATCACCTTCTTGATTCAGCAGGATACACTCTAGTAACTCAGGCAGGTCCCTCCTCCAGCCGTTG TATCACCTTCTTGATTCAGCAGGATACACTCTGGTAACTCAGGCAGGTCCCTCCTCCAGCCGTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:34382912..34383027 32194978 MeRIP-seq:(Medium) rs934994833 Functional Loss SNV dbSNP153 33..33 33 - - - 83923 RMVar_ID_83923 Human_SNP_ID_664205858 m1A Human chr19 + 34383378 34383378 34383378 GTCAGGTGAAGTCTGAGGAGCCAAAGCTATGTATGTGCATATGTCAGCCGGGCTCTGTGGGAGGT GTCAGGTGAAGTCTGAGGAGCCAAAGCTATGTCTGTGCATATGTCAGCCGGGCTCTGTGGGAGGT A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:34383376..34383525 26863196 MeRIP-seq:(Medium) rs536078770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53163,Human_RBP_ID_2563394,Human_RBP_ID_6803064,Human_RBP_ID_9086521,Human_RBP_ID_13431923,Human_RBP_ID_17131198,Human_RBP_ID_22969826,Human_RBP_ID_23792732 RMVar_hsa_circ_119814,RMVar_hsa_circ_194070,RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_372336,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_194092,RMVar_hsa_circ_46951,RMVar_hsa_circ_102405,RMVar_hsa_circ_194093 83924 RMVar_ID_83924 Human_SNP_ID_664206481 m1A Human chr19 - 34385949 34385938 34385950 CTCTACCTACCTGTAGTTGACCTTGGCTCCTTAAACCACACCTGAAAGACTATCTCTACCTACCT CTCTACCTACCTGTAGTTGACCTTGGCTCCT____________GAAAGACTATCTCTACCTACCT CAGGTGTGGTTTA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:34385947..34386177 26863196 MeRIP-seq:(Medium) rs774384349 Functional Loss DEL dbSNP153 32..43 33 - - - 83925 RMVar_ID_83925 Human_SNP_ID_664206642 m1A Human chr19 - 34386704 34386704 34386704 CTTGAGAGAGATACATCTACCTACCCACGTCTAACTTAGGGGCCACAGACCTCCTAGGAAACCCA CTTGAGAGAGATACATCTACCTACCCACGTCTCACTTAGGGGCCACAGACCTCCTAGGAAACCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:34386702..34386852 26863196 MeRIP-seq:(Medium) rs1475128469 Functional Loss SNV dbSNP153 33..33 33 - - - 83926 RMVar_ID_83926 Human_SNP_ID_664208595 m1A Human chr19 - 34392428 34392428 34392428 ACCAGGGCCAGATCCAACCACTTCAGACACTGACAGACTCAGGTCTTCATACCTGTATCAGATGC ACCAGGGCCAGATCCAACCACTTCAGACACTGGCAGACTCAGGTCTTCATACCTGTATCAGATGC T C lnc-SCGB2B2-12,lnc-SCGB2B2-12:2,lnc-SCGB2B2-12:3,lnc-SCGB2B2-12:4,lnc-SCGB2B2-12:5 RNACentral:URS0000D5A658,RNACentral:URS0000D571B2,RNACentral:URS0000D59B24,RNACentral:URS0000D5853B,RNACentral:URS0000D5A519 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34392426..34392975 26863196 MeRIP-seq:(Medium) rs1460417527 Functional Loss SNV dbSNP153 33..33 33 - - - 83927 RMVar_ID_83927 Human_SNP_ID_664208643 m1A Human chr19 - 34392520 34392520 34392520 CAGATCCTACTTCTTCAGACACTAGAAGACACAGACCCTCCTACCAGGGACAGATCCTACCTCCT CAGATCCTACTTCTTCAGACACTAGAAGACACCGACCCTCCTACCAGGGACAGATCCTACCTCCT T G lnc-SCGB2B2-12,lnc-SCGB2B2-12:2,lnc-SCGB2B2-12:3,lnc-SCGB2B2-12:4,lnc-SCGB2B2-12:5 RNACentral:URS0000D5A658,RNACentral:URS0000D571B2,RNACentral:URS0000D59B24,RNACentral:URS0000D5853B,RNACentral:URS0000D5A519 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:34392517..34392922 26863196 MeRIP-seq:(Medium) rs1280115874 Functional Loss SNV dbSNP153 33..33 33 - - - 83928 RMVar_ID_83928 Human_SNP_ID_664208922 m1A Human chr19 - 34393294 34393294 34393294 ACACAGAAACACACTCACCCACGTGCAGGGCAATGGAGAGTCCGATGGCCGACCACAGCGAGTAG ACACAGAAACACACTCACCCACGTGCAGGGCAGTGGAGAGTCCGATGGCCGACCACAGCGAGTAG T C lnc-SCGB2B2-12,lnc-SCGB2B2-12:2,lnc-SCGB2B2-12:3,lnc-SCGB2B2-12:4,lnc-SCGB2B2-12:5 RNACentral:URS0000D5A658,RNACentral:URS0000D571B2,RNACentral:URS0000D59B24,RNACentral:URS0000D5853B,RNACentral:URS0000D5A519 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:34393226..34393300 26863196 MeRIP-seq:(Medium) rs368458579 Functional Loss SNV dbSNP153 33..33 33 - - - 83929 RMVar_ID_83929 Human_SNP_ID_664209034 m1A Human chr19 - 34393693 34393693 34393693 GTGACACAAAAGCAGAGTCAACAGAAGTGGCCACACCCTGCGTCCTGTGGGCAGTGGGCACAGCT GTGACACAAAAGCAGAGTCAACAGAAGTGGCCGCACCCTGCGTCCTGTGGGCAGTGGGCACAGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34393690..34393802 26863196 MeRIP-seq:(Medium) rs772422583 Functional Loss SNV dbSNP153 33..33 33 - - - 83930 RMVar_ID_83930 Human_SNP_ID_664209187 m1A Human chr19 - 34394059 34394059 34394059 CAAGGCCTGGCTTGGCAGCTGGTACCTGCTGGAAGTACGCAGCAAAGCGGTGCAGGTACTGGTCA CAAGGCCTGGCTTGGCAGCTGGTACCTGCTGGTAGTACGCAGCAAAGCGGTGCAGGTACTGGTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34393869..34394107 26863196 MeRIP-seq:(Medium) rs755460923 Functional Loss SNV dbSNP153 33..33 33 - - - 83931 RMVar_ID_83931 Human_SNP_ID_664209191 m1A Human chr19 + 34394065 34394065 34394065 GTACCTGCACCGCTTTGCTGCGTACTTCCAGCAGGTACCAGCTGCCAAGCCAGGCCTTGGAGTCA GTACCTGCACCGCTTTGCTGCGTACTTCCAGCGGGTACCAGCTGCCAAGCCAGGCCTTGGAGTCA A G GPI Ensembl:ENSG00000105220 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:34393901..34394075 32194978 MeRIP-seq:(Medium) rs1324662373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9258998,Human_RBP_ID_9293616,Human_RBP_ID_17386772,Human_RBP_ID_18192178,Human_RBP_ID_19093072,Human_RBP_ID_22446646,Human_RBP_ID_22762915 Human_Splice_Rec_1990671,Human_Splice_Rec_1990705,Human_Splice_Rec_1990799,Human_Splice_Rec_1990833,Human_Splice_Rec_1990865,Human_Splice_Rec_1990897,Human_Splice_Rec_1990915,Human_Splice_Rec_1990919 RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_372336,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_194088,RMVar_hsa_circ_20222,RMVar_hsa_circ_194092,RMVar_hsa_circ_102405,RMVar_hsa_circ_86030,RMVar_hsa_circ_194093,RMVar_hsa_circ_84855,RMVar_hsa_circ_194097,RMVar_hsa_circ_101618,RMVar_hsa_circ_123589,RMVar_hsa_circ_194098,RMVar_hsa_circ_194099,RMVar_hsa_circ_194100 83932 RMVar_ID_83932 Human_SNP_ID_664209804 m1A Human chr19 + 34396540 34396540 34396540 GTGCCCTCCTCTAGGCCATATGGCTAGCTCCCATGGGCTGGGGTCATGTGGGTGACCACAGTGCC GTGCCCTCCTCTAGGCCATATGGCTAGCTCCCGTGGGCTGGGGTCATGTGGGTGACCACAGTGCC A G AC092073.1,GPI Ensembl:ENSG00000266953,Ensembl:ENSG00000105220 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34396536..34396694 26863196 MeRIP-seq:(Medium) rs1243832814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22359211,Human_RBP_ID_22545910,Human_RBP_ID_22591720 RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_297012,RMVar_hsa_circ_194082,RMVar_hsa_circ_124060,RMVar_hsa_circ_194089,RMVar_hsa_circ_194090,RMVar_hsa_circ_20222,RMVar_hsa_circ_194092,RMVar_hsa_circ_102405,RMVar_hsa_circ_86030,RMVar_hsa_circ_194093,RMVar_hsa_circ_194097,RMVar_hsa_circ_123589,RMVar_hsa_circ_194100,RMVar_hsa_circ_194101,RMVar_hsa_circ_273272 83933 RMVar_ID_83933 Human_SNP_ID_664210461 m1A Human chr19 + 34399261 34399261 34399261 CCCAGACAGAGGCCCTGATGAGGGGAAAATCGACGGAGGAGGCCCGAAAGGAGCTCCAGGCTGCG CCCAGACAGAGGCCCTGATGAGGGGAAAATCGGCGGAGGAGGCCCGAAAGGAGCTCCAGGCTGCG A G AC092073.1,GPI Ensembl:ENSG00000266953,Ensembl:ENSG00000105220 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34399181..34399348 26863196 MeRIP-seq:(Medium) rs1568351469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53184,Human_RBP_ID_913448,Human_RBP_ID_1560339,Human_RBP_ID_1884048,Human_RBP_ID_3954859,Human_RBP_ID_4519498,Human_RBP_ID_5117440,Human_RBP_ID_8483788,Human_RBP_ID_17271819,Human_RBP_ID_17386775,Human_RBP_ID_18192184,Human_RBP_ID_18728421,Human_RBP_ID_18997445,Human_RBP_ID_22446648 Human_Splice_Rec_1990676,Human_Splice_Rec_1990677,Human_Splice_Rec_1990710,Human_Splice_Rec_1990711,Human_Splice_Rec_1990804,Human_Splice_Rec_1990805,Human_Splice_Rec_1990836,Human_Splice_Rec_1990837,Human_Splice_Rec_1990902,Human_Splice_Rec_1990903,Human_Splice_Rec_1990924,Human_Splice_Rec_1990925 RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,RMVar_hsa_circ_88571,RMVar_hsa_circ_194081,RMVar_hsa_circ_120296,RMVar_hsa_circ_194082,RMVar_hsa_circ_124060,RMVar_hsa_circ_194090,RMVar_hsa_circ_194092,RMVar_hsa_circ_86030,RMVar_hsa_circ_194097,RMVar_hsa_circ_127789,RMVar_hsa_circ_123589,RMVar_hsa_circ_194100,RMVar_hsa_circ_104537,RMVar_hsa_circ_194102,RMVar_hsa_circ_194103 83934 RMVar_ID_83934 Human_SNP_ID_664210547 m1A Human chr19 - 34399557 34399557 34399557 CAATAGAGTTGGTTGGGCGATTTCCTTCAAAGACCTGCAGAAAACACCAAGGAATGTCTCCAAGA CAATAGAGTTGGTTGGGCGATTTCCTTCAAAGCCCTGCAGAAAACACCAAGGAATGTCTCCAAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:34399551..34399816 32194978 MeRIP-seq:(Medium) rs1358310553 Functional Loss SNV dbSNP153 33..33 33 - - - 83935 RMVar_ID_83935 Human_SNP_ID_664210749 m1A Human chr19 - 34400147 34400147 34400147 CCTTCCCTGCTAAGGGCTCGTGGTCCAAGCCCACAACCAGAGGGTGCTCTGGGTGGTGTCCAGGA CCTTCCCTGCTAAGGGCTCGTGGTCCAAGCCCGCAACCAGAGGGTGCTCTGGGTGGTGTCCAGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:34400100..34400213 26863196 MeRIP-seq:(Medium) rs980518904 Functional Loss SNV dbSNP153 33..33 33 - - - 83936 RMVar_ID_83936 Human_SNP_ID_664212249 m1A Human chr19 - 34404941 34404941 34404941 CTCTCTCTGGCACCTGCAGGCACTGGGAGCGGAACACCTTCCAGCTTCGGGGTGAAGACAAAGGG CTCTCTCTGGCACCTGCAGGCACTGGGAGCGGCACACCTTCCAGCTTCGGGGTGAAGACAAAGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:34404937..34409195 32194978 MeRIP-seq:(Medium) rs1568356756 Functional Loss SNV dbSNP153 33..33 33 - - - 83937 RMVar_ID_83937 Human_SNP_ID_664213424 m1A Human chr19 - 34409223 34409223 34409223 AAGGTAAACTGTGGTGAAGGCCCCTCCTCAGTATCACTTCCCCAGTCATCAGCACCTTCACACCA AAGGTAAACTGTGGTGAAGGCCCCTCCTCAGTGTCACTTCCCCAGTCATCAGCACCTTCACACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34409172..34409323 26863196 MeRIP-seq:(Medium) rs750174555 Functional Loss SNV dbSNP153 33..33 33 - - - 83938 RMVar_ID_83938 Human_SNP_ID_664220413 m1A Human chr19 - 34434959 34434959 34434959 AAAAAAATAAAACTTTTCTTTACCTTTTTGATAGTAGTTACTTGTCCAAGATACCCAGCTGTTCC AAAAAAATAAAACTTTTCTTTACCTTTTTGATTGTAGTTACTTGTCCAAGATACCCAGCTGTTCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:34434937..34450319 32194978 MeRIP-seq:(Medium) rs1449070289 Functional Loss SNV dbSNP153 33..33 33 - - - 83939 RMVar_ID_83939 Human_SNP_ID_664225420 m1A Human chr19 - 34452106 34452106 34452106 TATGAGCTCAGCTCCATCCCCCTTTTCTGCTAAATGAACTCTCAAAGTCTCGATGCTCTTTGAAA TATGAGCTCAGCTCCATCCCCCTTTTCTGCTACATGAACTCTCAAAGTCTCGATGCTCTTTGAAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34451976..34452150 26863196 MeRIP-seq:(Medium) rs770234024 Functional Loss SNV dbSNP153 33..33 33 - - - 83940 RMVar_ID_83940 Human_SNP_ID_664236282 m1A Human chr19 + 34490328 34490328 34490328 CGGTGTCAAGACGGGGAGTCCGTCGGTGTGGCATAGGCTGTGGCGCTAACCCCTGCTCTCTCCTG CGGTGTCAAGACGGGGAGTCCGTCGGTGTGGCGTAGGCTGTGGCGCTAACCCCTGCTCTCTCCTG A G WTIP Ensembl:ENSG00000142279 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34490325..34490401 26863196 MeRIP-seq:(Medium) rs1266100595 Functional Loss SNV dbSNP153 33..33 33 - - - 83941 RMVar_ID_83941 Human_SNP_ID_664239285 m1A Human chr19 - 34500211 34500211 34500211 GTGAGGGAAGAGGCCCAGGTTGGAGGCGCCGCAGGTGGCAACGACGACACAGTAGGTGGCCCGCC GTGAGGGAAGAGGCCCAGGTTGGAGGCGCCGCCGGTGGCAACGACGACACAGTAGGTGGCCCGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:34500162..34500408 26863196 MeRIP-seq:(Medium) rs1201645197 Functional Loss SNV dbSNP153 33..33 33 - - - 83942 RMVar_ID_83942 Human_SNP_ID_664239292 m1A Human chr19 + 34500224 34500224 34500224 CTGTGTCGTCGTTGCCACCTGCGGCGCCTCCAACCTGGGCCTCTTCCCTCACCCACTGTGCACGT CTGTGTCGTCGTTGCCACCTGCGGCGCCTCCAGCCTGGGCCTCTTCCCTCACCCACTGTGCACGT A G WTIP Ensembl:ENSG00000142279 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34500175..34500467 26863196 MeRIP-seq:(Medium) rs1412764169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519718,Human_RBP_ID_17921140 Human_Splice_Rec_1991132 RMVar_hsa_circ_125764,RMVar_hsa_circ_194182 83943 RMVar_ID_83943 Human_SNP_ID_664239509 m1A Human chr19 - 34500804 34500804 34500804 TGCAGGCCCCCTCCCCAAGGGTGTCACCCCTCACCCCCTCCTGGGACCCCGCCTAAACCAGGCAC TGCAGGCCCCCTCCCCAAGGGTGTCACCCCTCGCCCCCTCCTGGGACCCCGCCTAAACCAGGCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34500768..34500869 26863196 MeRIP-seq:(Medium) rs1353165388 Functional Loss SNV dbSNP153 33..33 33 - - - 83944 RMVar_ID_83944 Human_SNP_ID_664239539 m1A Human chr19 - 34500924 34500924 34500924 GGGGGGCCCAAGCCAGGAGCCCTGGAAGAGGGAGCAGGGCGGCAACTGGGGCCGCAAACACCCAT GGGGGGCCCAAGCCAGGAGCCCTGGAAGAGGGGGCAGGGCGGCAACTGGGGCCGCAAACACCCAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:34500875..34501064 26863196 MeRIP-seq:(Medium) rs1400102545 Functional Loss SNV dbSNP153 33..33 33 - - - 83945 RMVar_ID_83945 Human_SNP_ID_664240572 m1A Human chr19 + 34504213 34504213 34504213 ACTGAGTGACTCCGAGAATGAGGGGGAAAGATACGGAGACAGGATAAGCTGCAGAGAGAGAGGGA ACTGAGTGACTCCGAGAATGAGGGGGAAAGATCCGGAGACAGGATAAGCTGCAGAGAGAGAGGGA A C WTIP Ensembl:ENSG00000142279 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:34504164..34504265 32194978 MeRIP-seq:(Medium) rs1011663871 Functional Loss SNV dbSNP153 33..33 33 - - - 83946 RMVar_ID_83946 Human_SNP_ID_664240579 m1A Human chr19 + 34504235 34504232 34504236 GGGGAAAGATACGGAGACAGGATAAGCTGCAGAGAGAGAGGGAGAGAGGGATTGAACTGGAGCGA GGGGAAAGATACGGAGACAGGATAAGCTGC____AGAGAGGGAGAGAGGGATTGAACTGGAGCGA CAGAG C WTIP Ensembl:ENSG00000142279 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34504214..34504314 26863196 MeRIP-seq:(Medium) rs35854681 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_23793003 83947 RMVar_ID_83947 Human_SNP_ID_664240580 m1A Human chr19 + 34504235 34504232 34504236 GGGGAAAGATACGGAGACAGGATAAGCTGCAGAGAGAGAGGGAGAGAGGGATTGAACTGGAGCGA GGGGAAAGATACGGAGACAGGATAAGCTGCAG__AGAGAGGGAGAGAGGGATTGAACTGGAGCGA CAGAG CAG WTIP Ensembl:ENSG00000142279 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:34504214..34504314 26863196 MeRIP-seq:(Medium) rs35854681 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23793003 83948 RMVar_ID_83948 Human_SNP_ID_664306925 m1A Human chr19 - 34773167 34773167 34773167 TCCGCCGTTAGGTTGCGGCTGCTGTGGTTGCCAACGCTACACTGGGTAGAACGCCAGACAGGGGC TCCGCCGTTAGGTTGCGGCTGCTGTGGTTGCCGACGCTACACTGGGTAGAACGCCAGACAGGGGC T C ZNF599 Ensembl:ENSG00000153896 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34773116..34773184 26863196 MeRIP-seq:(Medium) rs1361102595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4520078,Human_RBP_ID_23793135 83949 RMVar_ID_83949 Human_SNP_ID_664352343 m1A Human chr19 - 34964086 34964086 34964086 GCAACTCTCCCGGCCGCCACGGTGGGGGCCGGAACTTCCTGCACTGCAGCCTCGCAGGTCATTTC GCAACTCTCCCGGCCGCCACGGTGGGGGCCGGGACTTCCTGCACTGCAGCCTCGCAGGTCATTTC T C ZNF792 Ensembl:ENSG00000180884 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34964055..34964213 26863196 MeRIP-seq:(Medium) rs1215729125 Functional Loss SNV dbSNP153 33..33 33 - - - 83950 RMVar_ID_83950 Human_SNP_ID_664352344 m1A Human chr19 - 34964086 34964086 34964086 GCAACTCTCCCGGCCGCCACGGTGGGGGCCGGAACTTCCTGCACTGCAGCCTCGCAGGTCATTTC GCAACTCTCCCGGCCGCCACGGTGGGGGCCGGCACTTCCTGCACTGCAGCCTCGCAGGTCATTTC T G ZNF792 Ensembl:ENSG00000180884 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:34964055..34964213 26863196 MeRIP-seq:(Medium) rs1215729125 Functional Loss SNV dbSNP153 33..33 33 - - - 83951 RMVar_ID_83951 Human_SNP_ID_664361441 m1A Human chr19 - 35000427 35000427 35000427 CGCCCCGGGCGCAGGGCAGGGCAGGGCAGGGCAGGGCTGGGCTGCGCGGGGCTGGGCTGCGCTGG CGCCCCGGGCGCAGGGCAGGGCAGGGCAGGGCTGGGCTGGGCTGCGCGGGGCTGGGCTGCGCTGG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:35000326..35000525;chr19:35000326..35001149 26863410 MeRIP-seq:(Medium) rs1423988132 Functional Loss SNV dbSNP153 33..33 33 - - - 83952 RMVar_ID_83952 Human_SNP_ID_664361473 m1A Human chr19 + 35000486 35000486 35000486 GGGGCGCGCCCACCGCGCCGCATCCATGTTCGAGTAAGGACCGGGCGACTAGAGCTCAGGGACCG GGGGCGCGCCCACCGCGCCGCATCCATGTTCGGGTAAGGACCGGGCGACTAGAGCTCAGGGACCG A G GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:35000395..35001199 26863410 MeRIP-seq:(Medium) rs1295131460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560168,Human_RBP_ID_5116848,Human_RBP_ID_13435274,Human_RBP_ID_17386782,Human_RBP_ID_18420909,Human_RBP_ID_19089914,Human_RBP_ID_23793243,Human_RBP_ID_26817386 Human_Splice_Rec_1991709,Human_Splice_Rec_1991747,Human_Splice_Rec_1991781,Human_Splice_Rec_1991789,Human_Splice_Rec_1991823 RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_194194,RMVar_hsa_circ_98872 83953 RMVar_ID_83953 Human_SNP_ID_664361584 m1A Human chr19 - 35000853 35000853 35000853 CTGGTCCCGATCCTGTCTCCATCCCAGGCCGGAGCCCCAGTTCGGCCTCGCGCTCACCCCTGGCT CTGGTCCCGATCCTGTCTCCATCCCAGGCCGGCGCCCCAGTTCGGCCTCGCGCTCACCCCTGGCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35000821..35000948 26863196 MeRIP-seq:(Medium) rs920923885 Functional Loss SNV dbSNP153 33..33 33 - - - 83954 RMVar_ID_83954 Human_SNP_ID_664362889 m1A Human chr19 + 35005866 35005866 35005866 CACGCATGAGCCAAAGTCCTGAAGGACAAATAAGGATTTGCTAGGCAAAGAAGAACTACGATCTG CACGCATGAGCCAAAGTCCTGAAGGACAAATACGGATTTGCTAGGCAAAGAAGAACTACGATCTG A C GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35005864..35005936 26863196 MeRIP-seq:(Medium) rs973542373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1560846,Human_RBP_ID_1884462,Human_RBP_ID_9916842 RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_194194,RMVar_hsa_circ_98872 83955 RMVar_ID_83955 Human_SNP_ID_664363129 m1A Human chr19 + 35006829 35006829 35006829 TAAACAAACAGTAAACAAGCAGGACACTCCAGATAGCCTGGGGTGTGGCGACAGAGGTGCCTGCC TAAACAAACAGTAAACAAGCAGGACACTCCAGGTAGCCTGGGGTGTGGCGACAGAGGTGCCTGCC A G GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35006826..35007075 26863196 MeRIP-seq:(Medium) rs1401459068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093988,Human_RBP_ID_6746110 RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_194194,RMVar_hsa_circ_98872 83956 RMVar_ID_83956 Human_SNP_ID_664363143 m1A Human chr19 - 35006862 35006862 35006862 TCAAATGCTCTCCTTCCGCATCATCCAGCCTAAGGCAGGCACCTCTGTCGCCACACCCCAGGCTA TCAAATGCTCTCCTTCCGCATCATCCAGCCTATGGCAGGCACCTCTGTCGCCACACCCCAGGCTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35006859..35006947 26863196 MeRIP-seq:(Medium) rs1032752348 Functional Loss SNV dbSNP153 33..33 33 - - - 83957 RMVar_ID_83957 Human_SNP_ID_664363706 m1A Human chr19 - 35009229 35009229 35009229 TCTCTGAGGAGCTATCTGATCCCTTCTCCACCATGGTGCCTGGTTCTGGCTCAGGTGGGGGCCGG TCTCTGAGGAGCTATCTGATCCCTTCTCCACCGTGGTGCCTGGTTCTGGCTCAGGTGGGGGCCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35009119..35009325 32194978 MeRIP-seq:(Medium) rs1205247273 Functional Loss SNV dbSNP153 33..33 33 - - - 83958 RMVar_ID_83958 Human_SNP_ID_664364935 m1A Human chr19 - 35013184 35013184 35013184 CAGCCAGAGCCCGGCCCGCCAGATTCCCCACCAGCCCTCGGCCTCCGCAGTTCCCCTGGCTTCCA CAGCCAGAGCCCGGCCCGCCAGATTCCCCACCGGCCCTCGGCCTCCGCAGTTCCCCTGGCTTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35013162..35013227 26863196 MeRIP-seq:(Medium) rs529891328 Functional Loss SNV dbSNP153 33..33 33 - - - 83959 RMVar_ID_83959 Human_SNP_ID_664365039 m1A Human chr19 + 35013409 35013409 35013409 GAGGTCAAAGGAGGTTGAAGGGTTCGGGGGAGAACAGGACGGTCGGCGTGCAGAGTTCCTGGAGT GAGGTCAAAGGAGGTTGAAGGGTTCGGGGGAGTACAGGACGGTCGGCGTGCAGAGTTCCTGGAGT A T GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35013360..35013532 26863196 MeRIP-seq:(Medium) rs780521482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911188,Human_RBP_ID_3956758,Human_RBP_ID_5117443,Human_RBP_ID_5371640,Human_RBP_ID_17695323,Human_RBP_ID_22416850,Human_RBP_ID_22662526 RMVar_hsa_circ_24218,RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_33948,RMVar_hsa_circ_101524,RMVar_hsa_circ_126536,RMVar_hsa_circ_194197,RMVar_hsa_circ_327218,RMVar_hsa_circ_51732,RMVar_hsa_circ_95906,RMVar_hsa_circ_194198,RMVar_hsa_circ_194199 83960 RMVar_ID_83960 Human_SNP_ID_664365139 m1A Human chr19 + 35013657 35013657 35013657 AGTGGGTTCGCGCCGTGGCCATGTCACGCCCAACCTTTCCCGAGCCAGCAGCGACGCAGACCATG AGTGGGTTCGCGCCGTGGCCATGTCACGCCCAGCCTTTCCCGAGCCAGCAGCGACGCAGACCATG A G GRAMD1A Ensembl:ENSG00000089351 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35013608..35013715 26863196 MeRIP-seq:(Medium) rs372725667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770269,Human_RBP_ID_5116850,Human_RBP_ID_18997467 Human_Splice_Rec_1991679,Human_Splice_Rec_1991725,Human_Splice_Rec_1991761,Human_Splice_Rec_1991803,Human_Splice_Rec_1991849,Human_Splice_Rec_1991851 Human_miRNA_ID_2084389 RMVar_hsa_circ_24218,RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_33948,RMVar_hsa_circ_101524,RMVar_hsa_circ_126536,RMVar_hsa_circ_194197,RMVar_hsa_circ_327218,RMVar_hsa_circ_51732,RMVar_hsa_circ_95906,RMVar_hsa_circ_194198,RMVar_hsa_circ_194199 83961 RMVar_ID_83961 Human_SNP_ID_664365349 m1A Human chr19 + 35014350 35014350 35014350 TTGGATCTGCTGCCCAGTGAGGAGCTATTGACAGACACAAGTAACTCCTCTTCATCCACTGGGGA TTGGATCTGCTGCCCAGTGAGGAGCTATTGACGGACACAAGTAACTCCTCTTCATCCACTGGGGA A G GRAMD1A Ensembl:ENSG00000089351 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:35014257..35014358 26863410 MeRIP-seq:(Medium) rs1334428022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1884479,Human_RBP_ID_27467149 Human_Splice_Rec_1991681,Human_Splice_Rec_1991727,Human_Splice_Rec_1991763,Human_Splice_Rec_1991805 Human_miRNA_ID_2930442 RMVar_hsa_circ_24218,RMVar_hsa_circ_25137,RMVar_hsa_circ_335962,RMVar_hsa_circ_33948,RMVar_hsa_circ_101524,RMVar_hsa_circ_126536,RMVar_hsa_circ_194197,RMVar_hsa_circ_327218,RMVar_hsa_circ_51732,RMVar_hsa_circ_95906,RMVar_hsa_circ_194198,RMVar_hsa_circ_194199 83962 RMVar_ID_83962 Human_SNP_ID_664367582 m1A Human chr19 - 35022035 35022035 35022035 TGTGGCCACTGCTCCTGTCTCTTACTCACACAATGCTGATGAGAACCAGGGCACTGGGGATGCCT TGTGGCCACTGCTCCTGTCTCTTACTCACACAGTGCTGATGAGAACCAGGGCACTGGGGATGCCT T C AC020907.4 Ensembl:ENSG00000271032 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35021986..35023429 26863196 MeRIP-seq:(Medium) rs369953090 Functional Loss SNV dbSNP153 33..33 33 - - - 83963 RMVar_ID_83963 Human_SNP_ID_664367583 m1A Human chr19 - 35022035 35022035 35022035 TGTGGCCACTGCTCCTGTCTCTTACTCACACAATGCTGATGAGAACCAGGGCACTGGGGATGCCT TGTGGCCACTGCTCCTGTCTCTTACTCACACACTGCTGATGAGAACCAGGGCACTGGGGATGCCT T G AC020907.4 Ensembl:ENSG00000271032 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35021986..35023429 26863196 MeRIP-seq:(Medium) rs369953090 Functional Loss SNV dbSNP153 33..33 33 - - - 83964 RMVar_ID_83964 Human_SNP_ID_664367727 m1A Human chr19 + 35022570 35022570 35022570 CAGCGGCGGCTTCCTCCCAGGCCAGAGGGGGCAGTCAGGATGGGCGTCCTGAGAGAGTGGAGACC CAGCGGCGGCTTCCTCCCAGGCCAGAGGGGGCGGTCAGGATGGGCGTCCTGAGAGAGTGGAGACC A G GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35022566..35022680 26863196 MeRIP-seq:(Medium) rs1289396797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239331,Human_RBP_ID_907664,Human_RBP_ID_3956763,Human_RBP_ID_8196412,Human_RBP_ID_8728403,Human_RBP_ID_8942437,Human_RBP_ID_9425289,Human_RBP_ID_18945336,Human_RBP_ID_22593856,Human_RBP_ID_22662530,Human_RBP_ID_25404469,Human_RBP_ID_26336156 RMVar_hsa_circ_24218,RMVar_hsa_circ_33948,RMVar_hsa_circ_101524,RMVar_hsa_circ_126536,RMVar_hsa_circ_194197,RMVar_hsa_circ_194198 83965 RMVar_ID_83965 Human_SNP_ID_664368312 m1A Human chr19 + 35024408 35024408 35024408 ATTCCCTCAGGCCCCAGTAGACTCAGGCCAGCAGTTGCGGTGGGTCAGAGCAAGTGTCAGGCCAG ATTCCCTCAGGCCCCAGTAGACTCAGGCCAGCGGTTGCGGTGGGTCAGAGCAAGTGTCAGGCCAG A G GRAMD1A Ensembl:ENSG00000089351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35024403..35024591 26863196 MeRIP-seq:(Medium) rs1025928591 Functional Loss SNV dbSNP153 33..33 33 - - - 83966 RMVar_ID_83966 Human_SNP_ID_664368724 m1A Human chr19 + 35026074 35026074 35026074 CCCGCAGATGAAGTTCTCGCTGGAGAAGCTGCACCAAGGCATCACAGTCTCAGACCCTCCCTTTG CCCGCAGATGAAGTTCTCGCTGGAGAAGCTGCGCCAAGGCATCACAGTCTCAGACCCTCCCTTTG A G GRAMD1A Ensembl:ENSG00000089351 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35026071..35026271 32194978 MeRIP-seq:(Medium) rs1370762276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1560877,Human_RBP_ID_8832451,Human_RBP_ID_13435503,Human_RBP_ID_18728905 Human_Splice_Rec_1991698,Human_Splice_Rec_1991746,Human_Splice_Rec_1991780,Human_Splice_Rec_1991822,Human_Splice_Rec_1991868 83967 RMVar_ID_83967 Human_SNP_ID_664405465 m1A Human chr19 + 35155531 35155531 35155531 AGGTCGGTCTCACTGACATCATGGCTGACCCCAGCATCGCCTGGTCCCACAGATGTCGCCCTCTG AGGTCGGTCTCACTGACATCATGGCTGACCCCGGCATCGCCTGGTCCCACAGATGTCGCCCTCTG A G FXYD5 Ensembl:ENSG00000089327 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:35155527..35156860 32194978 MeRIP-seq:(Medium) rs773974002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1992611,Human_Splice_Rec_1992619,Human_Splice_Rec_1992633,Human_Splice_Rec_1992649,Human_Splice_Rec_1992665,Human_Splice_Rec_1992681,Human_Splice_Rec_1992697,Human_Splice_Rec_1992713,Human_Splice_Rec_1992729,Human_Splice_Rec_1992745 RMVar_hsa_circ_77352,RMVar_hsa_circ_194214 83968 RMVar_ID_83968 Human_SNP_ID_664405479 m1A Human chr19 - 35155562 35155562 35155562 AGGCCAACGATGGTGAGAAGACACAGGCGACCAGAGGGCGACATCTGTGGGACCAGGCGATGCTG AGGCCAACGATGGTGAGAAGACACAGGCGACCTGAGGGCGACATCTGTGGGACCAGGCGATGCTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:35155551..35155625 26863196 MeRIP-seq:(Medium) rs766174267 Functional Loss SNV dbSNP153 33..33 33 - - - 83969 RMVar_ID_83969 Human_SNP_ID_664405502 m1A Human chr19 + 35155610 35155610 35155610 CTCACCATCGTTGGCCTGATTCTCCCCACCAGAGGTAAGACCCATCTCTGGCCTCCACCCTGCCC CTCACCATCGTTGGCCTGATTCTCCCCACCAGCGGTAAGACCCATCTCTGGCCTCCACCCTGCCC A C FXYD5 Ensembl:ENSG00000089327 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35155601..35155625 26863196 MeRIP-seq:(Medium) rs576135682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769561,Human_RBP_ID_4558356,Human_RBP_ID_17386790,Human_RBP_ID_26815684 Human_Splice_Rec_1992610,Human_Splice_Rec_1992611,Human_Splice_Rec_1992618,Human_Splice_Rec_1992619,Human_Splice_Rec_1992632,Human_Splice_Rec_1992633,Human_Splice_Rec_1992648,Human_Splice_Rec_1992649,Human_Splice_Rec_1992664,Human_Splice_Rec_1992665,Human_Splice_Rec_1992680,Human_Splice_Rec_1992681,Human_Splice_Rec_1992696,Human_Splice_Rec_1992697,Human_Splice_Rec_1992713,Human_Splice_Rec_1992728,Human_Splice_Rec_1992729,Human_Splice_Rec_1992744,Human_Splice_Rec_1992745 RMVar_hsa_circ_77352,RMVar_hsa_circ_194214 83970 RMVar_ID_83970 Human_SNP_ID_664406297 m1A Human chr19 + 35158378 35158378 35158378 GCAGTCTACACAGAACTCCAGCCCACCTCTCCAACCCCAACCTGGCCTGCTGATGGTGAGTAGTG GCAGTCTACACAGAACTCCAGCCCACCTCTCCGACCCCAACCTGGCCTGCTGATGGTGAGTAGTG A G FXYD5 Ensembl:ENSG00000089327 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35157365..35159546;chr19:35155483..35159546 26863196 MeRIP-seq:(Medium) rs1128882 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_770258,Human_RBP_ID_17268023,Human_RBP_ID_17386794,Human_RBP_ID_18728925,Human_RBP_ID_26817396 Human_Splice_Rec_1992614,Human_Splice_Rec_1992615,Human_Splice_Rec_1992622,Human_Splice_Rec_1992623,Human_Splice_Rec_1992636,Human_Splice_Rec_1992637,Human_Splice_Rec_1992652,Human_Splice_Rec_1992653,Human_Splice_Rec_1992668,Human_Splice_Rec_1992669,Human_Splice_Rec_1992684,Human_Splice_Rec_1992685,Human_Splice_Rec_1992702,Human_Splice_Rec_1992703,Human_Splice_Rec_1992716,Human_Splice_Rec_1992717,Human_Splice_Rec_1992732,Human_Splice_Rec_1992733,Human_Splice_Rec_1992748,Human_Splice_Rec_1992749 Human_miRNA_ID_2223908,Human_miRNA_ID_2223909,Human_miRNA_ID_2486978,Human_miRNA_ID_2486979,Human_miRNA_ID_3075343,Human_miRNA_ID_3075344 RMVar_hsa_circ_77352,RMVar_hsa_circ_122291,RMVar_hsa_circ_105676,RMVar_hsa_circ_194214,RMVar_hsa_circ_194215,RMVar_hsa_circ_194216 83971 RMVar_ID_83971 Human_SNP_ID_664406859 m1A Human chr19 + 35160716 35160716 35160716 CTCCTTGCTCTCCTGACCTGAATAGAAACACCACAACCCCAGACCCAGACCCAGCAACTGGAAGG CTCCTTGCTCTCCTGACCTGAATAGAAACACCGCAACCCCAGACCCAGACCCAGCAACTGGAAGG A G FXYD5 Ensembl:ENSG00000089327 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35160701..35160800 26863196 MeRIP-seq:(Medium) rs1369307976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52813,Human_RBP_ID_17271829,Human_RBP_ID_17386796,Human_RBP_ID_26336157,Human_RBP_ID_26817398 Human_Splice_Rec_1992624,Human_Splice_Rec_1992625,Human_Splice_Rec_1992638,Human_Splice_Rec_1992639,Human_Splice_Rec_1992654,Human_Splice_Rec_1992655,Human_Splice_Rec_1992670,Human_Splice_Rec_1992671,Human_Splice_Rec_1992686,Human_Splice_Rec_1992687,Human_Splice_Rec_1992704,Human_Splice_Rec_1992705,Human_Splice_Rec_1992718,Human_Splice_Rec_1992719,Human_Splice_Rec_1992734,Human_Splice_Rec_1992735,Human_Splice_Rec_1992750,Human_Splice_Rec_1992751,Human_Splice_Rec_1992759,Human_Splice_Rec_1992765 RMVar_hsa_circ_122291,RMVar_hsa_circ_194216 83972 RMVar_ID_83972 Human_SNP_ID_664407751 m1A Human chr19 + 35164154 35164154 35164154 CTCCTGCCCTCCACTGATCTGGCCACTCTCTCAGCTCATCCCACTGATGACACCACGACGCTCTC CTCCTGCCCTCCACTGATCTGGCCACTCTCTCGGCTCATCCCACTGATGACACCACGACGCTCTC A G FXYD5 Ensembl:ENSG00000089327 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:35164151..35164200 26863196 MeRIP-seq:(Medium) rs374770117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4520534,Human_RBP_ID_13435607 Human_Splice_Rec_1992627,Human_Splice_Rec_1992641,Human_Splice_Rec_1992657,Human_Splice_Rec_1992673,Human_Splice_Rec_1992689,Human_Splice_Rec_1992707,Human_Splice_Rec_1992721,Human_Splice_Rec_1992737,Human_Splice_Rec_1992753,Human_Splice_Rec_1992761,Human_Splice_Rec_1992769 RMVar_hsa_circ_122291,RMVar_hsa_circ_89205,RMVar_hsa_circ_194216,RMVar_hsa_circ_374057 83973 RMVar_ID_83973 Human_SNP_ID_664407763 m1A Human chr19 - 35164183 35164183 35164183 GGACGTCTGTGCTTGGGGATGGTCTCTCAGAGAGCGTCGTGGTGTCATCAGTGGGATGAGCTGAG GGACGTCTGTGCTTGGGGATGGTCTCTCAGAGGGCGTCGTGGTGTCATCAGTGGGATGAGCTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:35164151..35164250;chr19:35164176..35164200 26863196 MeRIP-seq:(Medium) rs981201088 Functional Loss SNV dbSNP153 33..33 33 - - - 83974 RMVar_ID_83974 Human_SNP_ID_664407784 m1A Human chr19 - 35164244 35164244 35164244 CTGTTTCCAGTCTGGGGAGGCAGTTACTAACCAGATGGCTTGAGGGTCTGGGGGTCTGTCTGGAC CTGTTTCCAGTCTGGGGAGGCAGTTACTAACCTGATGGCTTGAGGGTCTGGGGGTCTGTCTGGAC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:35164226..35164250 26863196 MeRIP-seq:(Medium) rs377234356 Functional Loss SNV dbSNP153 33..33 33 - - - 83975 RMVar_ID_83975 Human_SNP_ID_664409184 m1A Human chr19 + 35169851 35169851 35169851 TGGGGGCTGTCCCTCAAGTTATCTCCTCTGCTAAGACAAAAAGTAAAGCACTGTGGTCTTTGCCC TGGGGGCTGTCCCTCAAGTTATCTCCTCTGCTGAGACAAAAAGTAAAGCACTGTGGTCTTTGCCC A G FXYD5 Ensembl:ENSG00000089327 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35169801..35169850 26863196 MeRIP-seq:(Medium) rs1343106924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54974,Human_RBP_ID_17921373,Human_RBP_ID_26474818 Human_miRNA_ID_1121863 83976 RMVar_ID_83976 Human_SNP_ID_664428330 m1A Human chr19 + 35248811 35248811 35248811 AGTGTGGCTCGGAGGACCGCGGCGGGTCAAGCACCTTTCTCCCCCATATCTGAAAGCATGCCCTT AGTGTGGCTCGGAGGACCGCGGCGGGTCAAGCCCCTTTCTCCCCCATATCTGAAAGCATGCCCTT A C LSR Ensembl:ENSG00000105699 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35248760..35248900 26863196 MeRIP-seq:(Medium) rs964042030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5421430,Human_RBP_ID_5442985,Human_RBP_ID_5469647,Human_RBP_ID_5499399,Human_RBP_ID_27467160 83977 RMVar_ID_83977 Human_SNP_ID_664428335 m1A Human chr19 - 35248825 35248825 35248825 AAACGACGTGGACAAAGGGCATGCTTTCAGATATGGGGGAGAAAGGTGCTTGACCCGCCGCGGTC AAACGACGTGGACAAAGGGCATGCTTTCAGATGTGGGGGAGAAAGGTGCTTGACCCGCCGCGGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35248787..35248877 26863196 MeRIP-seq:(Medium) rs1420718566 Functional Loss SNV dbSNP153 33..33 33 - - - 83978 RMVar_ID_83978 Human_SNP_ID_664428489 m1A Human chr19 + 35249066 35249066 35249066 GGCCGGCGGGCTCTCCAGAGGGCTGGGCTCCCACCCGGCCGCCGCAGGCCGGGACGCGGTCGTCT GGCCGGCGGGCTCTCCAGAGGGCTGGGCTCCCCCCCGGCCGCCGCAGGCCGGGACGCGGTCGTCT A C LSR Ensembl:ENSG00000105699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35249018..35249147 26863196 MeRIP-seq:(Medium) rs1242239545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773723,Human_RBP_ID_4557446,Human_RBP_ID_5321608,Human_RBP_ID_22447676 Human_Splice_Rec_1992785,Human_Splice_Rec_1992801,Human_Splice_Rec_1992819,Human_Splice_Rec_1992839,Human_Splice_Rec_1992853,Human_Splice_Rec_1992885,Human_Splice_Rec_1992897,Human_Splice_Rec_1992915 83979 RMVar_ID_83979 Human_SNP_ID_664433822 m1A Human chr19 + 35267367 35267366 35267367 CGCCGAGTCAGGGAGCAGGTCTCCCACGAGTAATGGTGGGAGAAGCCGGGCCTACATGCCCCCGC CGCCGAGTCAGGGAGCAGGTCTCCCACGAGTGGTGGTGGGAGAAGCCGGGCCTACATGCCCCCGC AA GG LSR Ensembl:ENSG00000105699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35267316..35267400 26863196 MeRIP-seq:(Medium) rs865879834 Functional Loss MNV dbSNP153 32..33 33 - - - Human_miRNA_ID_2868808,Human_miRNA_ID_3096224 RMVar_hsa_circ_113935,RMVar_hsa_circ_125886,RMVar_hsa_circ_194221,RMVar_hsa_circ_194222 83980 RMVar_ID_83980 Human_SNP_ID_664433824 m1A Human chr19 + 35267367 35267367 35267367 CGCCGAGTCAGGGAGCAGGTCTCCCACGAGTAATGGTGGGAGAAGCCGGGCCTACATGCCCCCGC CGCCGAGTCAGGGAGCAGGTCTCCCACGAGTAGTGGTGGGAGAAGCCGGGCCTACATGCCCCCGC A G LSR Ensembl:ENSG00000105699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35267316..35267400 26863196 MeRIP-seq:(Medium) rs1568449511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2868808,Human_miRNA_ID_3096224 RMVar_hsa_circ_113935,RMVar_hsa_circ_125886,RMVar_hsa_circ_194221,RMVar_hsa_circ_194222 83981 RMVar_ID_83981 Human_SNP_ID_664433982 m1A Human chr19 - 35267602 35267601 35267603 CTCCTCCTCTCCTCCGACCCCTTCTTCCTCACAGCCTCCTCCAGTAGCCGCCCATCATAGGGGAG CTCCTCCTCTCCTCCGACCCCTTCTTCCTCA__GCCTCCTCCAGTAGCCGCCCATCATAGGGGAG CTG C HSALNG0125590 RNACentral:URS0000E99CF9 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35267551..35267686 26863196 MeRIP-seq:(Medium) rs774853932 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22233886 83982 RMVar_ID_83982 Human_SNP_ID_664434321 m1A Human chr19 + 35268174 35268150 35268175 CGCCCGCCTGCGTGCGCGCCCCGGCCCCGCCCAGGCGTGCGCATGCGCCCCGGCCCTCCGCCTTC CGCCCGCCT_________________________GCGTGCGCATGCGCCCCGGCCCTCCGCCTTC TGCGTGCGCGCCCCGGCCCCGCCCAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35268124..35268238 26863196 MeRIP-seq:(Medium) rs1337434035 Functional Loss DEL dbSNP153 10..34 33 - - - 83983 RMVar_ID_83983 Human_SNP_ID_664434583 m1A Human chr19 + 35268659 35268659 35268659 GCCAAGCCGGGCGGCGGCCGCGCGAGCCGGCGATCCAGGGCACTGGCGGCGGCCAGCCAGGGCGG GCCAAGCCGGGCGGCGGCCGCGCGAGCCGGCGGTCCAGGGCACTGGCGGCGGCCAGCCAGGGCGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:35268575..35268665 26863410 MeRIP-seq:(Medium) rs1438092179 Functional Loss SNV dbSNP153 33..33 33 - - - 83984 RMVar_ID_83984 Human_SNP_ID_664434680 m1A Human chr19 - 35268888 35268876 35268888 ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGCAGCCGCCGCCGCTCCTGCAGCCGCTGCAGCCGC ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGC____________TCCTGCAGCCGCTGCAGCCGC AGCGGCGGCGGCT A lnc-FAM187B-5 RNACentral:URS0000D57012 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:35268798..35268967 26863196 MeRIP-seq:(Medium) rs901349494 Functional Loss DEL dbSNP153 33..44 33 - - - 83985 RMVar_ID_83985 Human_SNP_ID_664434687 m1A Human chr19 - 35268888 35268879 35268888 ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGCAGCCGCCGCCGCTCCTGCAGCCGCTGCAGCCGC ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGC_________CGCTCCTGCAGCCGCTGCAGCCGC GGCGGCGGCT G lnc-FAM187B-5 RNACentral:URS0000D57012 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:35268798..35268967 26863196 MeRIP-seq:(Medium) rs1252884787 Functional Loss DEL dbSNP153 33..41 33 - - - 83986 RMVar_ID_83986 Human_SNP_ID_664434694 m1A Human chr19 - 35268888 35268888 35268888 ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGCAGCCGCCGCCGCTCCTGCAGCCGCTGCAGCCGC ATGTGAGGAGGAGATGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTCCTGCAGCCGCTGCAGCCGC T G lnc-FAM187B-5 RNACentral:URS0000D57012 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:35268798..35268967 26863196 MeRIP-seq:(Medium) rs1228190680 Functional Loss SNV dbSNP153 33..33 33 - - - 83987 RMVar_ID_83987 Human_SNP_ID_664434787 m1A Human chr19 - 35269061 35269061 35269061 CGGGGGCGGGGGGGGCGCGGGGCCCGGGGGGGAGGGGAGGGGAGGGGAGGGAGGGAGGGGAGGGG CGGGGGCGGGGGGGGCGCGGGGCCCGGGGGGGGGGGGAGGGGAGGGGAGGGAGGGAGGGGAGGGG T C lnc-FAM187B-3 RNACentral:URS00009BF8ED lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35269051..35269100 26863196 MeRIP-seq:(Medium) rs1296402100 Functional Loss SNV dbSNP153 33..33 33 - - - 83988 RMVar_ID_83988 Human_SNP_ID_664434998 m1A Human chr19 + 35269451 35269451 35269451 CCCTGCTCCCTCCTGTGCCCCTGGCAGCCACGACAAGGGACCCGAGGCGGAGGAGGGCGTCGAGC CCCTGCTCCCTCCTGTGCCCCTGGCAGCCACGGCAAGGGACCCGAGGCGGAGGAGGGCGTCGAGC A G USF2 Ensembl:ENSG00000105698 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35269426..35269450 26863196 MeRIP-seq:(Medium) rs1291617505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3956766,Human_RBP_ID_4558360,Human_RBP_ID_9328893 Human_Splice_Rec_1992942,Human_Splice_Rec_1992943,Human_Splice_Rec_1992960,Human_Splice_Rec_1992961,Human_Splice_Rec_1992976,Human_Splice_Rec_1992977,Human_Splice_Rec_1992994,Human_Splice_Rec_1992995,Human_Splice_Rec_1993008,Human_Splice_Rec_1993014,Human_Splice_Rec_1993015,Human_Splice_Rec_1993030,Human_Splice_Rec_1993031,Human_Splice_Rec_1993036,Human_Splice_Rec_1993037 RMVar_hsa_circ_194223,RMVar_hsa_circ_372147,RMVar_hsa_circ_373592,RMVar_hsa_circ_194224 83989 RMVar_ID_83989 Human_SNP_ID_664435092 m1A Human chr19 + 35269587 35269587 35269587 CGTGCCCCGACCCTCCTCGGCCCCAGGCGGGGACGGCCCAGGAGCGGAGGAGCAGACAGCGGTGG CGTGCCCCGACCCTCCTCGGCCCCAGGCGGGGGCGGCCCAGGAGCGGAGGAGCAGACAGCGGTGG A G USF2 Ensembl:ENSG00000105698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:35268523..35270000;chr19:35269076..35269738 26863196 MeRIP-seq:(Medium) rs767127112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825845,Human_RBP_ID_914031,Human_RBP_ID_4520704,Human_RBP_ID_5145735,Human_RBP_ID_9328894,Human_RBP_ID_18192196 Human_Splice_Rec_1992944,Human_Splice_Rec_1992962,Human_Splice_Rec_1992978,Human_Splice_Rec_1992996,Human_Splice_Rec_1993016,Human_Splice_Rec_1993032,Human_Splice_Rec_1993038 Human_miRNA_ID_2041477,Human_miRNA_ID_3020459 RMVar_hsa_circ_99001,RMVar_hsa_circ_194223,RMVar_hsa_circ_372147,RMVar_hsa_circ_373592,RMVar_hsa_circ_194224,RMVar_hsa_circ_117584,RMVar_hsa_circ_194226,RMVar_hsa_circ_98702,RMVar_hsa_circ_194227,RMVar_hsa_circ_194225 83990 RMVar_ID_83990 Human_SNP_ID_664435844 m1A Human chr19 + 35271110 35271110 35271110 TGTAGAAAAATTGATGGAACCAGAACACCCCGAGATGAGAGGAGAAGAGCCCAGCACAACGAAGG TGTAGAAAAATTGATGGAACCAGAACACCCCGTGATGAGAGGAGAAGAGCCCAGCACAACGAAGG A T USF2 Ensembl:ENSG00000105698 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35270701..35275120 26863196 MeRIP-seq:(Medium) rs143155018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1560920,Human_RBP_ID_1884513,Human_RBP_ID_8484271,Human_RBP_ID_13435746,Human_RBP_ID_17499083,Human_RBP_ID_18728969,Human_RBP_ID_26336162 Human_Splice_Rec_1992952,Human_Splice_Rec_1992953,Human_Splice_Rec_1992968,Human_Splice_Rec_1992969,Human_Splice_Rec_1992986,Human_Splice_Rec_1992987,Human_Splice_Rec_1993000,Human_Splice_Rec_1993001,Human_Splice_Rec_1993024,Human_Splice_Rec_1993025,Human_Splice_Rec_1993044,Human_Splice_Rec_1993045,Human_Splice_Rec_1993054,Human_Splice_Rec_1993055,Human_Splice_Rec_1993060,Human_Splice_Rec_1993061,Human_Splice_Rec_1993068,Human_Splice_Rec_1993069,Human_Splice_Rec_1993073,Human_Splice_Rec_1993079 Human_miRNA_ID_1358469 RMVar_hsa_circ_99001,RMVar_hsa_circ_373592,RMVar_hsa_circ_194224,RMVar_hsa_circ_27947,RMVar_hsa_circ_194226,RMVar_hsa_circ_98702,RMVar_hsa_circ_194227 83991 RMVar_ID_83991 Human_SNP_ID_664435855 m1A Human chr19 + 35271133 35271133 35271133 AACACCCCGAGATGAGAGGAGAAGAGCCCAGCACAACGAAGGTGAGGACAAGGTGTGGCTCCGGG AACACCCCGAGATGAGAGGAGAAGAGCCCAGCGCAACGAAGGTGAGGACAAGGTGTGGCTCCGGG A G USF2 Ensembl:ENSG00000105698 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35271053..35275120 26863196 MeRIP-seq:(Medium) rs1315462178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769641,Human_RBP_ID_825851,Human_RBP_ID_1560921,Human_RBP_ID_26336162 Human_Splice_Rec_1992952,Human_Splice_Rec_1992953,Human_Splice_Rec_1992968,Human_Splice_Rec_1992969,Human_Splice_Rec_1992986,Human_Splice_Rec_1992987,Human_Splice_Rec_1993000,Human_Splice_Rec_1993001,Human_Splice_Rec_1993024,Human_Splice_Rec_1993025,Human_Splice_Rec_1993044,Human_Splice_Rec_1993045,Human_Splice_Rec_1993054,Human_Splice_Rec_1993055,Human_Splice_Rec_1993060,Human_Splice_Rec_1993061,Human_Splice_Rec_1993068,Human_Splice_Rec_1993069,Human_Splice_Rec_1993073,Human_Splice_Rec_1993079 Human_miRNA_ID_1358469 RMVar_hsa_circ_99001,RMVar_hsa_circ_373592,RMVar_hsa_circ_194224,RMVar_hsa_circ_27947,RMVar_hsa_circ_194226,RMVar_hsa_circ_98702,RMVar_hsa_circ_194227 83992 RMVar_ID_83992 Human_SNP_ID_664446962 m1A Human chr19 - 35309881 35309881 35309881 GCTGCCGCGCAGTGGGACTCCAGGAGGAGCACAGGGGCGACTGCAGGGGCAAAATCAGGTCTGAG GCTGCCGCGCAGTGGGACTCCAGGAGGAGCACCGGGGCGACTGCAGGGGCAAAATCAGGTCTGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35309681..35309896 26863196 MeRIP-seq:(Medium) rs746129230 Functional Loss SNV dbSNP153 33..33 33 - - - 83993 RMVar_ID_83993 Human_SNP_ID_664447568 m1A Human chr19 - 35311963 35311963 35311963 GAGATGCGGAAGTCGCTGCTGAACAGGACGGGAGGGTTGTCCCCTGCCGAGAAGCTGGGGCTCTC GAGATGCGGAAGTCGCTGCTGAACAGGACGGGGGGGTTGTCCCCTGCCGAGAAGCTGGGGCTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35311874..35311970 26863196 MeRIP-seq:(Medium) rs983693393 Functional Loss SNV dbSNP153 33..33 33 - - - 83994 RMVar_ID_83994 Human_SNP_ID_664457215 m1A Human chr19 - 35346912 35346912 35346912 GGGTAGCAAGGAGAGTGGAAGAGAACAGGGGCAGGAGTTTTGGAGGTTTGGGGTTACCCTCACCA GGGTAGCAAGGAGAGTGGAAGAGAACAGGGGCCGGAGTTTTGGAGGTTTGGGGTTACCCTCACCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35346910..35347142 26863196 MeRIP-seq:(Medium) rs1425271125 Functional Loss SNV dbSNP153 33..33 33 - - - 83995 RMVar_ID_83995 Human_SNP_ID_664497373 m1A Human chr19 + 35500070 35500068 35500071 GAAGTGGGCATGGCGGTTAGAACAGACGGACGAAGGCCATTTTGCTCTGGAATAAACATCCCACC GAAGTGGGCATGGCGGTTAGAACAGACGGAC___GGCCATTTTGCTCTGGAATAAACATCCCACC CGAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35500063..35500218 26863196 MeRIP-seq:(Medium) rs1568560898 Functional Loss DEL dbSNP153 32..34 33 - - - 83996 RMVar_ID_83996 Human_SNP_ID_664499265 m1A Human chr19 - 35506187 35506186 35506187 GCCTTGGACATCGGTCCCCCTTTTCCCCACCCAGGGGCAAGGGTCGAGCTGGGGCAGTGGAGGAG GCCTTGGACATCGGTCCCCCTTTTCCCCACCC_GGGGCAAGGGTCGAGCTGGGGCAGTGGAGGAG CT C DMKN Ensembl:ENSG00000161249 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35506181..35506296 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 33..33 33 - - - Human_RBP_ID_240464,Human_RBP_ID_5373735,Human_RBP_ID_25404779 Human_Splice_Rec_1993909,Human_Splice_Rec_1993945,Human_Splice_Rec_1993993,Human_Splice_Rec_1994117,Human_Splice_Rec_1994141,Human_Splice_Rec_1994211,Human_Splice_Rec_1994253,Human_Splice_Rec_1994275,Human_Splice_Rec_1994353,Human_Splice_Rec_1994379,Human_Splice_Rec_1994495,Human_Splice_Rec_1994519,Human_Splice_Rec_1994585 RMVar_hsa_circ_110986,RMVar_hsa_circ_194230,RMVar_hsa_circ_377738 83997 RMVar_ID_83997 Human_SNP_ID_664500408 m1A Human chr19 + 35510449 35510449 35510449 ATTCCGAGCATGGAGAAGGCCAGGTGTGGCCGAGGGTATTCGGAACTACGCAATGATTTGGAGAA ATTCCGAGCATGGAGAAGGCCAGGTGTGGCCGTGGGTATTCGGAACTACGCAATGATTTGGAGAA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:35510284..35510450 26863196 MeRIP-seq:(Medium) rs761604228 Functional Loss SNV dbSNP153 33..33 33 - - - 83998 RMVar_ID_83998 Human_SNP_ID_664510696 m1A Human chr19 + 35545723 35545723 35545723 AGACGCCGCCTCGCGATCCCCGCGCGGGCGGGACCGGGCGGCCGGCATCATGACCCTGTTTCACT AGACGCCGCCTCGCGATCCCCGCGCGGGCGGGGCCGGGCGGCCGGCATCATGACCCTGTTTCACT A G TMEM147 Ensembl:ENSG00000105677 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Wild Type;HTR8/Svneo,Normoxia chr19:35545626..35545800;chr19:35545651..35545991 26863410,32194978 MeRIP-seq:(Medium) rs1376192323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825535,Human_RBP_ID_4521058,Human_RBP_ID_18420912,Human_RBP_ID_22066629 Human_Splice_Rec_1994699,Human_Splice_Rec_1994707,Human_Splice_Rec_1994729,Human_Splice_Rec_1994739,Human_Splice_Rec_1994743,Human_Splice_Rec_1994747,Human_Splice_Rec_1994755 Human_miRNA_ID_2618295 RMVar_hsa_circ_86463,RMVar_hsa_circ_194237 83999 RMVar_ID_83999 Human_SNP_ID_664518921 m1A Human chr19 + 35575668 35575668 35575668 ATATAGACAGCAGGACGGTGGCCATGGAAGTCAGAATCCACTAAGGAGTGTGTAACAACTCACCT ATATAGACAGCAGGACGGTGGCCATGGAAGTCGGAATCCACTAAGGAGTGTGTAACAACTCACCT A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12461385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270099,Human_RBP_ID_1064019,Human_RBP_ID_1094881,Human_RBP_ID_2563908,Human_RBP_ID_4566598,Human_RBP_ID_5193934,Human_RBP_ID_5293490,Human_RBP_ID_5588335,Human_RBP_ID_6803195,Human_RBP_ID_8255983,Human_RBP_ID_9086862,Human_RBP_ID_9917015,Human_RBP_ID_10483790,Human_RBP_ID_17063374,Human_RBP_ID_17068515,Human_RBP_ID_17131334,Human_RBP_ID_17191053,Human_RBP_ID_17695345,Human_RBP_ID_18179870,Human_RBP_ID_22391199,Human_RBP_ID_23310171,Human_RBP_ID_25404981,Human_RBP_ID_26474835 Human_Splice_Rec_1994838 84000 RMVar_ID_84000 Human_SNP_ID_664518936 m1A Human chr19 + 35575732 35575732 35575732 TGCCGAATCAACTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCC TGCCGAATCAACTAGCCCTGAAAATGGATGGCGCTGGAGCATCAGGCCCATACCCGGCCATCGCC A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62109965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064019,Human_RBP_ID_5190631,Human_RBP_ID_5293555,Human_RBP_ID_5421445,Human_RBP_ID_5443003,Human_RBP_ID_5499418,Human_RBP_ID_8096729,Human_RBP_ID_17063375,Human_RBP_ID_17921490,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26467462,Human_RBP_ID_26749474,Human_RBP_ID_27157562 84001 RMVar_ID_84001 Human_SNP_ID_664518980 m1A Human chr19 + 35575852 35575852 35575852 CTATTCTCAAACTTTAAATGGGCAAGAAGCCCAGCTAGCTCAGTCGGTAGAGCATAAGACTCTTA CTATTCTCAAACTTTAAATGGGCAAGAAGCCCGGCTAGCTCAGTCGGTAGAGCATAAGACTCTTA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEK293T cells, from four datasets;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr19:35575804..35575930;chr19:35575801..35575932 29072297,26863196 m1A-MAP:(High) rs79125255 Functional Loss SNV dbSNP153 33..33 33 - - - 84002 RMVar_ID_84002 Human_SNP_ID_664528013 m1A Human chr19 + 35612795 35612795 35612795 GAGGGAGGCGGTGTCGCCGCCGCGGCGCTGTCATGGAGCTAGCGCAGGAAGCGCGGGAACTGGGT GAGGGAGGCGGTGTCGCCGCCGCGGCGCTGTCGTGGAGCTAGCGCAGGAAGCGCGGGAACTGGGT A G HAUS5 Ensembl:ENSG00000249115 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35612726..35612947 26863196 MeRIP-seq:(Medium) rs1319571858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558366,Human_RBP_ID_17921496,Human_RBP_ID_18420913,Human_RBP_ID_26334901 Human_Splice_Rec_1994907,Human_Splice_Rec_1994943,Human_Splice_Rec_1994975,Human_Splice_Rec_1994977,Human_Splice_Rec_1995011,Human_Splice_Rec_1995047,Human_Splice_Rec_1995057 84003 RMVar_ID_84003 Human_SNP_ID_664528017 m1A Human chr19 - 35612802 35612802 35612802 CCCAGCAACCCAGTTCCCGCGCTTCCTGCGCTAGCTCCATGACAGCGCCGCGGCGGCGACACCGC CCCAGCAACCCAGTTCCCGCGCTTCCTGCGCTGGCTCCATGACAGCGCCGCGGCGGCGACACCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:35612751..35612951;chr19:35612751..35612943 26863196 MeRIP-seq:(Medium) rs1008063144 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 84004 RMVar_ID_84004 Human_SNP_ID_664528298 m1A Human chr19 + 35613791 35613790 35613791 GGGCCTACATCTTGCAGCATGTGCACAGTCAGAGGTAAGCTGGGCTAGAGCAGGGGAGGGGGCAC GGGCCTACATCTTGCAGCATGTGCACAGTCAG_GGTAAGCTGGGCTAGAGCAGGGGAGGGGGCAC GA G HAUS5 Ensembl:ENSG00000249115 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35613768..35613918 32194978 MeRIP-seq:(Medium) rs1265144825 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3956772,Human_RBP_ID_5370285,Human_RBP_ID_18729104,Human_RBP_ID_18997514,Human_RBP_ID_19089953 Human_Splice_Rec_1994908,Human_Splice_Rec_1994909,Human_Splice_Rec_1994944,Human_Splice_Rec_1994945,Human_Splice_Rec_1994976,Human_Splice_Rec_1994978,Human_Splice_Rec_1994979,Human_Splice_Rec_1995012,Human_Splice_Rec_1995013,Human_Splice_Rec_1995049,Human_Splice_Rec_1995058,Human_Splice_Rec_1995059 84005 RMVar_ID_84005 Human_SNP_ID_664530122 m1A Human chr19 - 35619900 35619900 35619900 TTCAAGGTGGGTCTGGGGACTAGGATGCCAAGACCAGGGCTGCTGACCCAAGGGTGAGGTCTGGC TTCAAGGTGGGTCTGGGGACTAGGATGCCAAGGCCAGGGCTGCTGACCCAAGGGTGAGGTCTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35619894..35620027 26863196 MeRIP-seq:(Medium) rs1160171700 Functional Loss SNV dbSNP153 33..33 33 - - - 84006 RMVar_ID_84006 Human_SNP_ID_664532561 m1A Human chr19 + 35629121 35629121 35629121 ACAGCAGAACCAGCGGCGGCGGCTAAGCAGAGACTGTAGTAGCGGCGACAGCGACGACGGCAGCG ACAGCAGAACCAGCGGCGGCGGCTAAGCAGAGGCTGTAGTAGCGGCGACAGCGACGACGGCAGCG A G RBM42 Ensembl:ENSG00000126254 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35629051..35629314 26863196 MeRIP-seq:(Medium) rs1431630081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139969,Human_RBP_ID_241494,Human_RBP_ID_4521232,Human_RBP_ID_5117466,Human_RBP_ID_9329985,Human_RBP_ID_13436580,Human_RBP_ID_26988715 84007 RMVar_ID_84007 Human_SNP_ID_664532562 m1A Human chr19 - 35629125 35629125 35629125 CCATCGCTGCCGTCGTCGCTGTCGCCGCTACTACAGTCTCTGCTTAGCCGCCGCCGCTGGTTCTG CCATCGCTGCCGTCGTCGCTGTCGCCGCTACTGCAGTCTCTGCTTAGCCGCCGCCGCTGGTTCTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:35629069..35629242 26863196 MeRIP-seq:(Medium) rs996320214 Functional Loss SNV dbSNP153 33..33 33 - - - 84008 RMVar_ID_84008 Human_SNP_ID_664532576 m1A Human chr19 + 35629171 35629171 35629171 GCGACGACGGCAGCGATGGCTGGGGCGGGGCCAGCCCCGGGACTCCCGGGTGCAGGAGGACCCGT GCGACGACGGCAGCGATGGCTGGGGCGGGGCCGGCCCCGGGACTCCCGGGTGCAGGAGGACCCGT A G RBM42 Ensembl:ENSG00000126254 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:35629076..35629250 26863410 MeRIP-seq:(Medium) rs1277287927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139969,Human_RBP_ID_241494,Human_RBP_ID_773798,Human_RBP_ID_4557457,Human_RBP_ID_5117466,Human_RBP_ID_8839975,Human_RBP_ID_9329985,Human_RBP_ID_17921522,Human_RBP_ID_22446654 84009 RMVar_ID_84009 Human_SNP_ID_664532662 m1A Human chr19 - 35629480 35629480 35629480 AGTAGAACAGACATCAGCGCTCAGGACCTCGTACCAATTTTGGAACTGTGGGTATATCGCGAGGG AGTAGAACAGACATCAGCGCTCAGGACCTCGTGCCAATTTTGGAACTGTGGGTATATCGCGAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35629477..35629675 26863196 MeRIP-seq:(Medium) rs747736261 Functional Loss SNV dbSNP153 33..33 33 - - - 84010 RMVar_ID_84010 Human_SNP_ID_664532698 m1A Human chr19 - 35629579 35629579 35629579 CTTCTACTGTGGGGACCGTGGGGACAGTGGGCACCGCAGGCACAGCAGTTGGGATTCCAGGTACT CTTCTACTGTGGGGACCGTGGGGACAGTGGGCCCCGCAGGCACAGCAGTTGGGATTCCAGGTACT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:35629501..35629660 32194978 MeRIP-seq:(Medium) rs747782038 Functional Loss SNV dbSNP153 33..33 33 - - - 84011 RMVar_ID_84011 Human_SNP_ID_664533619 m1A Human chr19 + 35633012 35633012 35633012 CCCCACGTGCTACAGAGAGCAGGTGAGGGGCCAGGGTCATCATCCCTGCCACATAACTCCCCCCA CCCCACGTGCTACAGAGAGCAGGTGAGGGGCCGGGGTCATCATCCCTGCCACATAACTCCCCCCA A G RBM42 Ensembl:ENSG00000126254 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35633006..35633089 26863196 MeRIP-seq:(Medium) rs1330942309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1995124 RMVar_hsa_circ_75560,RMVar_hsa_circ_113838,RMVar_hsa_circ_194252,RMVar_hsa_circ_194253 84012 RMVar_ID_84012 Human_SNP_ID_664533878 m1A Human chr19 - 35633833 35633833 35633833 AGGGCCAGCGGCAGGCTGGGCCCAATGACTGCAGGGCCAGCTGGGGCACCTCCTGCCCCCACGGC AGGGCCAGCGGCAGGCTGGGCCCAATGACTGCCGGGCCAGCTGGGGCACCTCCTGCCCCCACGGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35633784..35633939 26863196 MeRIP-seq:(Medium) rs1442714651 Functional Loss SNV dbSNP153 33..33 33 - - - 84013 RMVar_ID_84013 Human_SNP_ID_664538095 m1A Human chr19 + 35648402 35648402 35648402 ATTGAGCTGCAGGTTGAATCCGGGGTGCCTTTAGGTGAGTGTGGAGGGTTCTGTAACCTGGGACC ATTGAGCTGCAGGTTGAATCCGGGGTGCCTTTCGGTGAGTGTGGAGGGTTCTGTAACCTGGGACC A C COX6B1 Ensembl:ENSG00000126267 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:35648351..35648472 26863410 MeRIP-seq:(Medium) rs1378592267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1014955,Human_RBP_ID_4557458,Human_RBP_ID_5145182,Human_RBP_ID_5320323,Human_RBP_ID_9086877,Human_RBP_ID_9328897,Human_RBP_ID_19093146,Human_RBP_ID_23211245 Human_Splice_Rec_1995265 RMVar_hsa_circ_125126,RMVar_hsa_circ_194257 84014 RMVar_ID_84014 Human_SNP_ID_664556585 m1A Human chr19 - 35716440 35716440 35716440 GCGGTCGGAAGGGGAGGCCGGTGAAGGAAGGAAGAAGGCGGCGAAAGCTGGCCAAGTTAGGGGTG GCGGTCGGAAGGGGAGGCCGGTGAAGGAAGGAGGAAGGCGGCGAAAGCTGGCCAAGTTAGGGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35716264..35716801 26863196 MeRIP-seq:(Medium) rs928844453 Functional Loss SNV dbSNP153 33..33 33 - - - 84015 RMVar_ID_84015 Human_SNP_ID_664557181 m1A Human chr19 - 35718171 35718171 35718171 CCGGGCTCGGCTCCGCCCGGCCCCGTCGCGCCACCGCCGCGCCGCAGAGCTACCCGCACTCTTTC CCGGGCTCGGCTCCGCCCGGCCCCGTCGCGCCCCCGCCGCGCCGCAGAGCTACCCGCACTCTTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:35718026..35718466;chr19:35718026..35720096;chr19:35718056..35720098 26863196 MeRIP-seq:(Medium) rs189776176 Functional Loss SNV dbSNP153 33..33 33 - - - 84016 RMVar_ID_84016 Human_SNP_ID_664557745 m1A Human chr19 - 35719778 35719777 35719778 TGCGACCCCGACCTCGGGGCGCTCGACCTAAAAGGAGAATAGTTGTGGGGAGATGGATCAAGCCA TGCGACCCCGACCTCGGGGCGCTCGACCTAAA_GGAGAATAGTTGTGGGGAGATGGATCAAGCCA CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35719776..35719925 26863196 MeRIP-seq:(Medium) rs765159714 Functional Loss DEL dbSNP153 33..33 33 - - - 84017 RMVar_ID_84017 Human_SNP_ID_664557747 m1A Human chr19 - 35719778 35719778 35719778 TGCGACCCCGACCTCGGGGCGCTCGACCTAAAAGGAGAATAGTTGTGGGGAGATGGATCAAGCCA TGCGACCCCGACCTCGGGGCGCTCGACCTAAAGGGAGAATAGTTGTGGGGAGATGGATCAAGCCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35719776..35719925 26863196 MeRIP-seq:(Medium) rs753578199 Functional Loss SNV dbSNP153 33..33 33 - - - 84018 RMVar_ID_84018 Human_SNP_ID_664557893 m1A Human chr19 + 35720070 35720070 35720070 TGCAGGAGGAAGCAGCAAGCAGTAGTGGTGGCAGAAGCAGCTGTGACAATCCCCAAACCTGAGCC TGCAGGAGGAAGCAGCAAGCAGTAGTGGTGGCTGAAGCAGCTGTGACAATCCCCAAACCTGAGCC A T KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35719786..35720071 26863196 MeRIP-seq:(Medium) rs759362058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26336173,Human_RBP_ID_26770037,Human_RBP_ID_27815371 Human_miRNA_ID_2239821,Human_miRNA_ID_3017117 RMVar_hsa_circ_125026,RMVar_hsa_circ_194262 84019 RMVar_ID_84019 Human_SNP_ID_664558265 m1A Human chr19 - 35720802 35720802 35720802 GTGGGAGGAGAGGTGCCCTCTGGCCCTGCCCGAGCAGCTTCCCGCTCCGCCCGCTGGCTGGGAGT GTGGGAGGAGAGGTGCCCTCTGGCCCTGCCCGGGCAGCTTCCCGCTCCGCCCGCTGGCTGGGAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35720752..35721124 26863196 MeRIP-seq:(Medium) rs1376226885 Functional Loss SNV dbSNP153 33..33 33 - - - 84020 RMVar_ID_84020 Human_SNP_ID_664558435 m1A Human chr19 + 35721121 35721121 35721121 CCTCTCCACCACGTGCCCCAACTCCTCCATCTACCCCAGTTCCACTCCCTGAGAAGAGACGGTCC CCTCTCCACCACGTGCCCCAACTCCTCCATCTCCCCCAGTTCCACTCCCTGAGAAGAGACGGTCC A C KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:35721036..35721209 26863196 MeRIP-seq:(Medium) rs1235952423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54771,Human_RBP_ID_915141,Human_RBP_ID_1884669,Human_RBP_ID_5130360,Human_RBP_ID_5320327,Human_RBP_ID_9328902,Human_RBP_ID_17081810,Human_RBP_ID_18945348,Human_RBP_ID_22071955 RMVar_hsa_circ_125026,RMVar_hsa_circ_194262 84021 RMVar_ID_84021 Human_SNP_ID_664558571 m1A Human chr19 + 35721336 35721336 35721336 ACCCCAAGCGAAGCCCACCTGAAGATCTACGAATCGGTGCTTACTCCTCCTCCTCTTGGGGCTCC ACCCCAAGCGAAGCCCACCTGAAGATCTACGAGTCGGTGCTTACTCCTCCTCCTCTTGGGGCTCC A G KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35721285..35721385 32194978 MeRIP-seq:(Medium) rs1365644925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1884670,Human_RBP_ID_5130361,Human_RBP_ID_6746845,Human_RBP_ID_8840584,Human_RBP_ID_17010221,Human_RBP_ID_17083131,Human_RBP_ID_17268067,Human_RBP_ID_18532383,Human_RBP_ID_22970625 RMVar_hsa_circ_125026,RMVar_hsa_circ_194262 84022 RMVar_ID_84022 Human_SNP_ID_664558728 m1A Human chr19 - 35721626 35721626 35721626 GAGGCATCTGCTGTGGTGACGGCGGTGGCTGCAGCTGTGGCTGTGGTGGCGGTAGTGCCTGGGGC GAGGCATCTGCTGTGGTGACGGCGGTGGCTGCGGCTGTGGCTGTGGTGGCGGTAGTGCCTGGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35721540..35721629;chr19:35721502..35721730 26863196 MeRIP-seq:(Medium) rs1453478048 Functional Loss SNV dbSNP153 33..33 33 - - - 84023 RMVar_ID_84023 Human_SNP_ID_664559088 m1A Human chr19 + 35722472 35722472 35722472 GAGTCGGTGGAAGCTAAGAGAGAGCGGCCCTCAGTATGCATCGGGAGGAGGGCCCTGAAGAAGAC GAGTCGGTGGAAGCTAAGAGAGAGCGGCCCTCCGTATGCATCGGGAGGAGGGCCCTGAAGAAGAC A C KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35722443..35722553 26863196 MeRIP-seq:(Medium) rs757864454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911243 Human_Splice_Rec_1995395,Human_Splice_Rec_1995467 RMVar_hsa_circ_125026,RMVar_hsa_circ_39808,RMVar_hsa_circ_194262 84024 RMVar_ID_84024 Human_SNP_ID_664559089 m1A Human chr19 + 35722472 35722472 35722472 GAGTCGGTGGAAGCTAAGAGAGAGCGGCCCTCAGTATGCATCGGGAGGAGGGCCCTGAAGAAGAC GAGTCGGTGGAAGCTAAGAGAGAGCGGCCCTCGGTATGCATCGGGAGGAGGGCCCTGAAGAAGAC A G KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35722443..35722553 26863196 MeRIP-seq:(Medium) rs757864454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911243 Human_Splice_Rec_1995395,Human_Splice_Rec_1995467 RMVar_hsa_circ_125026,RMVar_hsa_circ_39808,RMVar_hsa_circ_194262 84025 RMVar_ID_84025 Human_SNP_ID_664559624 m1A Human chr19 + 35723859 35723859 35723859 GGGGGGCCCCGGGAGGAGGTGGTGGCCCACCCAGGGCCCGAGGAGCAGGACTCCCTCCTGCAGCG GGGGGGCCCCGGGAGGAGGTGGTGGCCCACCCGGGGCCCGAGGAGCAGGACTCCCTCCTGCAGCG A G KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35723814..35723949 26863196 MeRIP-seq:(Medium) rs933436092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773226,Human_RBP_ID_909558,Human_RBP_ID_4521513,Human_RBP_ID_5373755,Human_RBP_ID_9294390,Human_RBP_ID_18729249,Human_RBP_ID_24559896,Human_RBP_ID_27839538 RMVar_hsa_circ_1554,RMVar_hsa_circ_39808,RMVar_hsa_circ_14568 84026 RMVar_ID_84026 Human_SNP_ID_664562445 m1A Human chr19 + 35731584 35731584 35731584 CGGGGCGGGCGGGAGCGTCTGATGTGGCTTGGATGCACCAGGCAAGTAAGAAAGTGGTAGGACTG CGGGGCGGGCGGGAGCGTCTGATGTGGCTTGGGTGCACCAGGCAAGTAAGAAAGTGGTAGGACTG A G KMT2B Ensembl:ENSG00000272333 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35731568..35731712 26863196 MeRIP-seq:(Medium) rs904152395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196415 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84027 RMVar_ID_84027 Human_SNP_ID_664562446 m1A Human chr19 + 35731584 35731584 35731584 CGGGGCGGGCGGGAGCGTCTGATGTGGCTTGGATGCACCAGGCAAGTAAGAAAGTGGTAGGACTG CGGGGCGGGCGGGAGCGTCTGATGTGGCTTGGTTGCACCAGGCAAGTAAGAAAGTGGTAGGACTG A T KMT2B Ensembl:ENSG00000272333 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35731568..35731712 26863196 MeRIP-seq:(Medium) rs904152395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196415 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84028 RMVar_ID_84028 Human_SNP_ID_664563170 m1A Human chr19 - 35733086 35733086 35733086 TTGGATGTGGCGGGTTTGGGGGGCTCAGGGGCAGGGCCAAGGCTTAACACCCGGACCCCTGGGGC TTGGATGTGGCGGGTTTGGGGGGCTCAGGGGCCGGGCCAAGGCTTAACACCCGGACCCCTGGGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35733035..35733335 32194978 MeRIP-seq:(Medium) rs754415548 Functional Loss SNV dbSNP153 33..33 33 - - - 84029 RMVar_ID_84029 Human_SNP_ID_664563288 m1A Human chr19 + 35733290 35733290 35733290 GGCCCCCTCCTCGGCGTGCTGCCCGTGGTCGGAGTGGTCCGCCCTGCCCCGCCCCCGCCACCCCC GGCCCCCTCCTCGGCGTGCTGCCCGTGGTCGGTGTGGTCCGCCCTGCCCCGCCCCCGCCACCCCC A T KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:35733286..35733450 26863196 MeRIP-seq:(Medium) rs1359689959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_520153,Human_RBP_ID_17081813 Human_miRNA_ID_3066388 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84030 RMVar_ID_84030 Human_SNP_ID_664563322 m1A Human chr19 + 35733330 35733330 35733330 GCCCTGCCCCGCCCCCGCCACCCCCTCCCCTGACGCTGGTGCTGAGCAGTGGGCCAGCCAGCCCG GCCCTGCCCCGCCCCCGCCACCCCCTCCCCTGCCGCTGGTGCTGAGCAGTGGGCCAGCCAGCCCG A C KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35733319..35733549 26863196 MeRIP-seq:(Medium) rs1377293557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240893,Human_RBP_ID_520153 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84031 RMVar_ID_84031 Human_SNP_ID_664563323 m1A Human chr19 + 35733330 35733330 35733330 GCCCTGCCCCGCCCCCGCCACCCCCTCCCCTGACGCTGGTGCTGAGCAGTGGGCCAGCCAGCCCG GCCCTGCCCCGCCCCCGCCACCCCCTCCCCTGGCGCTGGTGCTGAGCAGTGGGCCAGCCAGCCCG A G KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35733319..35733549 26863196 MeRIP-seq:(Medium) rs1377293557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240893,Human_RBP_ID_520153 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84032 RMVar_ID_84032 Human_SNP_ID_664563333 m1A Human chr19 + 35733345 35733345 35733345 CGCCACCCCCTCCCCTGACGCTGGTGCTGAGCAGTGGGCCAGCCAGCCCGCCCCGCCAGGCCATC CGCCACCCCCTCCCCTGACGCTGGTGCTGAGCGGTGGGCCAGCCAGCCCGCCCCGCCAGGCCATC A G KMT2B Ensembl:ENSG00000272333 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:35733285..35733385 26863410 MeRIP-seq:(Medium) rs948721320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240893,Human_RBP_ID_1372858 RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84033 RMVar_ID_84033 Human_SNP_ID_664563602 m1A Human chr19 - 35733869 35733869 35733869 AGGAGGGAGAGGGCAAGGCCGGTCCCTACCTGAATAGTGGTGCCACTGGGACTCAAGCAGCAGGT AGGAGGGAGAGGGCAAGGCCGGTCCCTACCTGCATAGTGGTGCCACTGGGACTCAAGCAGCAGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35733634..35735257 32194978 MeRIP-seq:(Medium) rs1257830103 Functional Loss SNV dbSNP153 33..33 33 - - - 84034 RMVar_ID_84034 Human_SNP_ID_664563773 m1A Human chr19 + 35734395 35734395 35734395 GTGGCACAGGGTGGGGCGTTGTGTCCAAGTCCAGAATTGAGACCATGGTTGAAGAAGGCAAAACA GTGGCACAGGGTGGGGCGTTGTGTCCAAGTCCGGAATTGAGACCATGGTTGAAGAAGGCAAAACA A G KMT2B Ensembl:ENSG00000272333 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35734366..35734753;chr19:35734384..35734745 26863196 MeRIP-seq:(Medium) rs550115004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1554,RMVar_hsa_circ_194265,RMVar_hsa_circ_128079 84035 RMVar_ID_84035 Human_SNP_ID_664564616 m1A Human chr19 - 35737256 35737256 35737256 AGGCATCACACCCCAGACCTCTCACCGGAGATAGACCTCTGCCCGAGCAGCCCCATGGGGATTCA AGGCATCACACCCCAGACCTCTCACCGGAGATGGACCTCTGCCCGAGCAGCCCCATGGGGATTCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35736953..35737506 32194978 MeRIP-seq:(Medium) rs759465949 Functional Loss SNV dbSNP153 33..33 33 - - - 84036 RMVar_ID_84036 Human_SNP_ID_664565079 m1A Human chr19 - 35738624 35738624 35738624 TGAGATGCTCTGGGAGGGGCTAGGGAGCCCCCAGGCTAGGGGCAAGATGGCAGCGACGGCAGCAG TGAGATGCTCTGGGAGGGGCTAGGGAGCCCCCGGGCTAGGGGCAAGATGGCAGCGACGGCAGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35738578..35738728 32194978 MeRIP-seq:(Medium) rs893252735 Functional Loss SNV dbSNP153 33..33 33 - - - 84037 RMVar_ID_84037 Human_SNP_ID_664565320 m1A Human chr19 + 35739344 35739344 35739344 TGGACAGCACCCGCAATGCATCTGCCCGCCCTAGCTGGGCGAGGTGTGTGCCAAGCTGGCCCAGG TGGACAGCACCCGCAATGCATCTGCCCGCCCTGGCTGGGCGAGGTGTGTGCCAAGCTGGCCCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35739300..35739400 32194978 MeRIP-seq:(Medium) rs754681421 Functional Loss SNV dbSNP153 33..33 33 - - - 84038 RMVar_ID_84038 Human_SNP_ID_664565449 m1A Human chr19 + 35739548 35739548 35739548 CCATACCCCCACCTGGCCCAGGCTCAGGGTCCAGCAGTACAATCAGCTCTTCCAGCACCTCCAGC CCATACCCCCACCTGGCCCAGGCTCAGGGTCCGGCAGTACAATCAGCTCTTCCAGCACCTCCAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35739498..35739779 32194978 MeRIP-seq:(Medium) rs199514116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18729312 84039 RMVar_ID_84039 Human_SNP_ID_664565450 m1A Human chr19 + 35739548 35739548 35739548 CCATACCCCCACCTGGCCCAGGCTCAGGGTCCAGCAGTACAATCAGCTCTTCCAGCACCTCCAGC CCATACCCCCACCTGGCCCAGGCTCAGGGTCCTGCAGTACAATCAGCTCTTCCAGCACCTCCAGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35739498..35739779 32194978 MeRIP-seq:(Medium) rs199514116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18729312 84040 RMVar_ID_84040 Human_SNP_ID_664565898 m1A Human chr19 - 35740454 35740454 35740454 GGCAGTGCAACCCCGACGGCGCGGAGCTATGTAGCCCCTGCGGCGGCGGAGCCGTGACCCCTACT GGCAGTGCAACCCCGACGGCGCGGAGCTATGTGGCCCCTGCGGCGGCGGAGCCGTGACCCCTACT T C AD000671.2,IGFLR1 Ensembl:ENSG00000267120,Ensembl:ENSG00000126246 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:35740057..35740545;chr19:35740422..35740536 26863196 MeRIP-seq:(Medium) rs1403564106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1995641,Human_Splice_Rec_1995657,Human_Splice_Rec_1995665,Human_Splice_Rec_1995669,Human_Splice_Rec_1995677,Human_Splice_Rec_1995681,Human_Splice_Rec_1995703 84041 RMVar_ID_84041 Human_SNP_ID_664567637 m1A Human chr19 - 35744670 35744670 35744670 TTCTGTGCAGACCATAGTGCTGCTCAACCTGTACCGGAATCCACAGAACACAGCCCAAACTGCAG TTCTGTGCAGACCATAGTGCTGCTCAACCTGTGCCGGAATCCACAGAACACAGCCCAAACTGCAG T C AD000671.2,U2AF1L4 Ensembl:ENSG00000267120,Ensembl:ENSG00000161265 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:35744663..35745198 32194978 MeRIP-seq:(Medium) rs1454612982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1561270,Human_RBP_ID_1884714,Human_RBP_ID_3568836,Human_RBP_ID_13436911 Human_Splice_Rec_1995690,Human_Splice_Rec_1995691,Human_Splice_Rec_1995717,Human_Splice_Rec_1995739,Human_Splice_Rec_1995756,Human_Splice_Rec_1995757,Human_Splice_Rec_1995774,Human_Splice_Rec_1995775,Human_Splice_Rec_1995784,Human_Splice_Rec_1995785,Human_Splice_Rec_1995796,Human_Splice_Rec_1995797,Human_Splice_Rec_1995807,Human_Splice_Rec_1995830,Human_Splice_Rec_1995831,Human_Splice_Rec_1995860,Human_Splice_Rec_1995861,Human_Splice_Rec_1995870,Human_Splice_Rec_1995874,Human_Splice_Rec_1995875 RMVar_hsa_circ_8090,RMVar_hsa_circ_194271 84042 RMVar_ID_84042 Human_SNP_ID_664567713 m1A Human chr19 + 35744883 35744883 35744883 GAGGGGACTGGCAAGGATGAACAGCGGGATGGAAGGGACTGGCAAAGATGAACAGCCGCCGTGTG GAGGGGACTGGCAAGGATGAACAGCGGGATGGTAGGGACTGGCAAAGATGAACAGCCGCCGTGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35744881..35744977 26863196 MeRIP-seq:(Medium) rs975983683 Functional Loss SNV dbSNP153 33..33 33 - - - 84043 RMVar_ID_84043 Human_SNP_ID_664567822 m1A Human chr19 - 35745147 35745147 35745147 CTGCCGGCACGGGGACCGGTGCTCCCGGCTTCACAACAAGCCGACATTCAGCCAGGTGAGACCCG CTGCCGGCACGGGGACCGGTGCTCCCGGCTTCTCAACAAGCCGACATTCAGCCAGGTGAGACCCG T A AD000671.2,U2AF1L4 Ensembl:ENSG00000267120,Ensembl:ENSG00000161265 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35745113..35745413 26863196 MeRIP-seq:(Medium) rs1433440809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4521788,Human_RBP_ID_17921623,Human_RBP_ID_25444625 Human_Splice_Rec_1995688,Human_Splice_Rec_1995689,Human_Splice_Rec_1995708,Human_Splice_Rec_1995709,Human_Splice_Rec_1995730,Human_Splice_Rec_1995731,Human_Splice_Rec_1995744,Human_Splice_Rec_1995745,Human_Splice_Rec_1995754,Human_Splice_Rec_1995755,Human_Splice_Rec_1995773,Human_Splice_Rec_1995783,Human_Splice_Rec_1995794,Human_Splice_Rec_1995795,Human_Splice_Rec_1995820,Human_Splice_Rec_1995828,Human_Splice_Rec_1995829,Human_Splice_Rec_1995838,Human_Splice_Rec_1995839,Human_Splice_Rec_1995848,Human_Splice_Rec_1995852,Human_Splice_Rec_1995858,Human_Splice_Rec_1995859,Human_Splice_Rec_1995868,Human_Splice_Rec_1995869,Human_Splice_Rec_1995878,Human_Splice_Rec_1995879,Human_Splice_Rec_1995881 RMVar_hsa_circ_8090,RMVar_hsa_circ_194271 84044 RMVar_ID_84044 Human_SNP_ID_664568090 m1A Human chr19 - 35745699 35745699 35745699 ACTAGGGTGGGCGAAACGACCCCCAACTCACCAGGAGAGCTCACTTCCTCCGGCTGGGGTGCCTT ACTAGGGTGGGCGAAACGACCCCCAACTCACCGGGAGAGCTCACTTCCTCCGGCTGGGGTGCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35745611..35745946;chr19:35745611..35746000;chr19:35745661..35745960 26863196 MeRIP-seq:(Medium) rs1399211770 Functional Loss SNV dbSNP153 33..33 33 - - - 84045 RMVar_ID_84045 Human_SNP_ID_664568311 m1A Human chr19 - 35746486 35746486 35746486 TTGATTTGGCTCTGTTCTGTGTAGGCTGGGACAAGGAAGGCCTCTCGGAAGAACCAGAAGATGTT TTGATTTGGCTCTGTTCTGTGTAGGCTGGGACGAGGAAGGCCTCTCGGAAGAACCAGAAGATGTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:35746435..35752187 32194978 MeRIP-seq:(Medium) rs1256573314 Functional Loss SNV dbSNP153 33..33 33 - - - 84046 RMVar_ID_84046 Human_SNP_ID_664568431 m1A Human chr19 - 35746804 35746804 35746804 CCAGGGGTATGGTGAAGGAGAGGTAGTCCCCAAGGGCACCCCAGCGGGGCCGGTAGATCTGGAAG CCAGGGGTATGGTGAAGGAGAGGTAGTCCCCAGGGGCACCCCAGCGGGGCCGGTAGATCTGGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35746701..35746871 32194978 MeRIP-seq:(Medium) rs1196358066 Functional Loss SNV dbSNP153 33..33 33 - - - 84047 RMVar_ID_84047 Human_SNP_ID_664569337 m1A Human chr19 - 35749955 35749955 35749955 AACAAACCTGACCCTGATCTTCCCTTGCTTGGAAACTTCCATGACTCCACAGCACCCAGGGGTGG AACAAACCTGACCCTGATCTTCCCTTGCTTGGCAACTTCCATGACTCCACAGCACCCAGGGGTGG T G AD000671.3 Ensembl:ENSG00000267439 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35749945..35750076 26863196 MeRIP-seq:(Medium) rs771753736 Functional Loss SNV dbSNP153 33..33 33 - - - 84048 RMVar_ID_84048 Human_SNP_ID_664570769 m1A Human chr19 - 35755270 35755270 35755270 CACCGACAACTCCCCGGCTTCCAGACCCTACCAGCACTACCCTAACCCTCAGCCGACAGTCTCAG CACCGACAACTCCCCGGCTTCCAGACCCTACCGGCACTACCCTAACCCTCAGCCGACAGTCTCAG T C HSPB6 Ensembl:ENSG00000004776 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35755207..35755396 26863196 MeRIP-seq:(Medium) rs1472072834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126744,RMVar_hsa_circ_194282,RMVar_hsa_circ_110709,RMVar_hsa_circ_194281 84049 RMVar_ID_84049 Human_SNP_ID_664571149 m1A Human chr19 - 35756208 35756208 35756208 AGGGACCCGGGGCTCTGAGGAGGGAGCTGGGGAATCAGTGCCCTGGGGGGCACGATGACTTCGGA AGGGACCCGGGGCTCTGAGGAGGGAGCTGGGGGATCAGTGCCCTGGGGGGCACGATGACTTCGGA T C HSPB6 Ensembl:ENSG00000004776 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35756179..35756301 26863196 MeRIP-seq:(Medium) rs1226740341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126744,RMVar_hsa_circ_194282 84050 RMVar_ID_84050 Human_SNP_ID_664571866 m1A Human chr19 + 35758225 35758214 35758225 GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCAGGTGAGGCCGATCGCTCTTCCAGGGACTACAG GGAAGCGCGGAGGGAGCCGCGG___________GGTGAGGCCGATCGCTCTTCCAGGGACTACAG GGATGGACCGCA G PROSER3 Ensembl:ENSG00000167595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35758209..35758314;chr19:35758199..35758352 26863196 MeRIP-seq:(Medium) rs1285208667 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_240509,Human_RBP_ID_1561307,Human_RBP_ID_5373777,Human_RBP_ID_6746984,Human_RBP_ID_19089987 Human_Splice_Rec_1996005,Human_Splice_Rec_1996013,Human_Splice_Rec_1996033,Human_Splice_Rec_1996045,Human_Splice_Rec_1996049,Human_Splice_Rec_1996057,Human_Splice_Rec_1996075,Human_Splice_Rec_1996083 84051 RMVar_ID_84051 Human_SNP_ID_664571875 m1A Human chr19 + 35758225 35758225 35758225 GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCAGGTGAGGCCGATCGCTCTTCCAGGGACTACAG GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCCGGTGAGGCCGATCGCTCTTCCAGGGACTACAG A C PROSER3 Ensembl:ENSG00000167595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35758209..35758314;chr19:35758199..35758352 26863196 MeRIP-seq:(Medium) rs752035115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240509,Human_RBP_ID_1561307,Human_RBP_ID_5373777,Human_RBP_ID_6746984,Human_RBP_ID_19089987 Human_Splice_Rec_1996005,Human_Splice_Rec_1996013,Human_Splice_Rec_1996033,Human_Splice_Rec_1996045,Human_Splice_Rec_1996049,Human_Splice_Rec_1996057,Human_Splice_Rec_1996075,Human_Splice_Rec_1996083 84052 RMVar_ID_84052 Human_SNP_ID_664571876 m1A Human chr19 + 35758225 35758225 35758225 GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCAGGTGAGGCCGATCGCTCTTCCAGGGACTACAG GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCGGGTGAGGCCGATCGCTCTTCCAGGGACTACAG A G PROSER3 Ensembl:ENSG00000167595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35758209..35758314;chr19:35758199..35758352 26863196 MeRIP-seq:(Medium) rs752035115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240509,Human_RBP_ID_1561307,Human_RBP_ID_5373777,Human_RBP_ID_6746984,Human_RBP_ID_19089987 Human_Splice_Rec_1996005,Human_Splice_Rec_1996013,Human_Splice_Rec_1996033,Human_Splice_Rec_1996045,Human_Splice_Rec_1996049,Human_Splice_Rec_1996057,Human_Splice_Rec_1996075,Human_Splice_Rec_1996083 84053 RMVar_ID_84053 Human_SNP_ID_664571877 m1A Human chr19 + 35758225 35758225 35758225 GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCAGGTGAGGCCGATCGCTCTTCCAGGGACTACAG GGAAGCGCGGAGGGAGCCGCGGGATGGACCGCTGGTGAGGCCGATCGCTCTTCCAGGGACTACAG A T PROSER3 Ensembl:ENSG00000167595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35758209..35758314;chr19:35758199..35758352 26863196 MeRIP-seq:(Medium) rs752035115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240509,Human_RBP_ID_1561307,Human_RBP_ID_5373777,Human_RBP_ID_6746984,Human_RBP_ID_19089987 Human_Splice_Rec_1996005,Human_Splice_Rec_1996013,Human_Splice_Rec_1996033,Human_Splice_Rec_1996045,Human_Splice_Rec_1996049,Human_Splice_Rec_1996057,Human_Splice_Rec_1996075,Human_Splice_Rec_1996083 84054 RMVar_ID_84054 Human_SNP_ID_664574427 m1A Human chr19 - 35767350 35767350 35767350 GAGGCCGGGGGTTCGAGGGTGGAGGCCAGGGAAGCCGGGGGCGCGAGGGTAGAGCCCAGATGTGC GAGGCCGGGGGTTCGAGGGTGGAGGCCAGGGAGGCCGGGGGCGCGAGGGTAGAGCCCAGATGTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35767272..35767517 26863196 MeRIP-seq:(Medium) rs1044112585 Functional Loss SNV dbSNP153 33..33 33 - - - 84055 RMVar_ID_84055 Human_SNP_ID_664579314 m1A Human chr19 - 35783420 35783420 35783420 TTAGTGCAGTCTTCCTCACCCACTTTATTCAAAACTGTACACTCCCTTCTCTGTACCCCTGGCCT TTAGTGCAGTCTTCCTCACCCACTTTATTCAAGACTGTACACTCCCTTCTCTGTACCCCTGGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35783139..35783983 26863196 MeRIP-seq:(Medium) rs1476072697 Functional Loss SNV dbSNP153 33..33 33 - - - 84056 RMVar_ID_84056 Human_SNP_ID_664579676 m1A Human chr19 - 35784598 35784598 35784598 GGCCGGGGCGGGGTCAAGTCTGGGGACCTCCCACCTCCTCCCAGGTGGACCCATGGCCCCAAGCG GGCCGGGGCGGGGTCAAGTCTGGGGACCTCCCCCCTCCTCCCAGGTGGACCCATGGCCCCAAGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35784548..35784637 26863196 MeRIP-seq:(Medium) rs534615652 Functional Loss SNV dbSNP153 33..33 33 - - - 84057 RMVar_ID_84057 Human_SNP_ID_664580422 m1A Human chr19 + 35786800 35786800 35786800 TGCCTCTGCCTTCCCACCCAGGGTGACCCCCCAGGCCATCTCGCCCCGGGGGCCCACCAGCCCCG TGCCTCTGCCTTCCCACCCAGGGTGACCCCCCCGGCCATCTCGCCCCGGGGGCCCACCAGCCCCG A C ARHGAP33 Ensembl:ENSG00000004777 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35786751..35786966 26863196 MeRIP-seq:(Medium) rs1264884889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5130366,Human_RBP_ID_5373781,Human_RBP_ID_17083137,Human_RBP_ID_24552837 84058 RMVar_ID_84058 Human_SNP_ID_664580680 m1A Human chr19 + 35787332 35787332 35787332 CCGAGCAACAGAGCCAGCAGGAGTGTGGGGGCACCCCACCTGCTTCCCAATCCCCCTTCCACCGC CCGAGCAACAGAGCCAGCAGGAGTGTGGGGGCGCCCCACCTGCTTCCCAATCCCCCTTCCACCGC A G ARHGAP33 Ensembl:ENSG00000004777 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35787283..35787539 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_miRNA_ID_1504308 84059 RMVar_ID_84059 Human_SNP_ID_664580851 m1A Human chr19 - 35787683 35787677 35787683 TGGCTTGGGGACCCCGAGGAAGGGTGGCAGGCACTCCCTGGGGGCTGGGGAGAAGAAGCCGGGGG TGGCTTGGGGACCCCGAGGAAGGGTGGCAGGC______TGGGGGCTGGGGAGAAGAAGCCGGGGG AGGGAGT A LINC01529 Ensembl:ENSG00000225872 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35787648..35787738 26863196 MeRIP-seq:(Medium) rs1318910533 Functional Loss DEL dbSNP153 33..38 33 - - - 84060 RMVar_ID_84060 Human_SNP_ID_664580907 m1A Human chr19 + 35787811 35787810 35787811 TCTCTGGGCCCCCCTGCACCACTCGACAGGGGAGAGAACCTGTACTATGAGATCGGGGCAAGTGA TCTCTGGGCCCCCCTGCACCACTCGACAGGGG_GAGAACCTGTACTATGAGATCGGGGCAAGTGA GA G ARHGAP33 Ensembl:ENSG00000004777 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35787581..35788028 32194978 MeRIP-seq:(Medium) rs1224047179 Functional Loss DEL dbSNP153 33..33 33 - - - 84061 RMVar_ID_84061 Human_SNP_ID_664580957 m1A Human chr19 - 35787917 35787917 35787917 GAGTGGGGGTGATTGGCCAAGCATGCCGTAGGAGGCATTGAGCCTGTCGGGGGGCATGGAGCGAA GAGTGGGGGTGATTGGCCAAGCATGCCGTAGGCGGCATTGAGCCTGTCGGGGGGCATGGAGCGAA T G LINC01529 Ensembl:ENSG00000225872 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35787868..35788150 26863196 MeRIP-seq:(Medium) rs189751869 Functional Loss SNV dbSNP153 33..33 33 - - - 84062 RMVar_ID_84062 Human_SNP_ID_664604683 m1A Human chr19 + 35868613 35868613 35868613 CGCTGGGGCCGGGCCGGGCGGGAGTGCAGGGGACGTGAGGGCGCAAGGGCCGGGACATGGGGCCC CGCTGGGGCCGGGCCGGGCGGGAGTGCAGGGGGCGTGAGGGCGCAAGGGCCGGGACATGGGGCCC A G APLP1 Ensembl:ENSG00000105290 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:35868537..35868633 26863410 MeRIP-seq:(Medium) rs1278463195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4522149 84063 RMVar_ID_84063 Human_SNP_ID_664604710 m1A Human chr19 - 35868695 35868686 35868695 GAAGCAGCAGCAATAGTGGCAGCAGCAGCGGCAGCGGCGGCTGGCCCGGGCGGCGACTTAGACCG GAAGCAGCAGCAATAGTGGCAGCAGCAGCGGC_________TGGCCCGGGCGGCGACTTAGACCG AGCCGCCGCT A NPHS1 Ensembl:ENSG00000161270 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35868540..35868804 26863196 MeRIP-seq:(Medium) rs1210473529 Functional Loss DEL dbSNP153 33..41 33 - - - 84064 RMVar_ID_84064 Human_SNP_ID_664604718 m1A Human chr19 + 35868711 35868711 35868711 CCGGGCCAGCCGCCGCTGCCGCTGCTGCTGCCACTATTGCTGCTGCTTCTGCGCGCGCAGCCCGC CCGGGCCAGCCGCCGCTGCCGCTGCTGCTGCCCCTATTGCTGCTGCTTCTGCGCGCGCAGCCCGC A C APLP1 Ensembl:ENSG00000105290 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:35868533..35868804;chr19:35868537..35868791 26863196 MeRIP-seq:(Medium) rs1029662234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4522155 Human_Splice_Rec_1996765,Human_Splice_Rec_1996797,Human_Splice_Rec_1996829 84065 RMVar_ID_84065 Human_SNP_ID_664605047 m1A Human chr19 + 35869747 35869747 35869747 CACCGGGACCTGCGCACCGGCCGCTGGGAACCAGACCCACAGCGCTCTCGACGCTGTCTCCGGGA CACCGGGACCTGCGCACCGGCCGCTGGGAACCGGACCCACAGCGCTCTCGACGCTGTCTCCGGGA A G APLP1 Ensembl:ENSG00000105290 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35869696..35870219 32194978 MeRIP-seq:(Medium) rs778721019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241346 Human_Splice_Rec_1996734,Human_Splice_Rec_1996735,Human_Splice_Rec_1996767,Human_Splice_Rec_1996798,Human_Splice_Rec_1996799,Human_Splice_Rec_1996830,Human_Splice_Rec_1996831,Human_Splice_Rec_1996861 84066 RMVar_ID_84066 Human_SNP_ID_664607160 m1A Human chr19 - 35876540 35876540 35876540 AGCAGGCCCAGGCTCTGATTCACCCTCTCCTCAATCACTTGAAGGTGGGTATGCACCTGTGGGTG AGCAGGCCCAGGCTCTGATTCACCCTCTCCTCCATCACTTGAAGGTGGGTATGCACCTGTGGGTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35872535..35878534 32194978 MeRIP-seq:(Medium) rs1290989727 Functional Loss SNV dbSNP153 33..33 33 - - - 84067 RMVar_ID_84067 Human_SNP_ID_664610948 m1A Human chr19 + 35890084 35890084 35890084 GGCCTGGAAAAGTAAGGGGAGGGCTGGTGGGGATCTGGGCTCAGCTGGCCCAGGCCTCTAAACTG GGCCTGGAAAAGTAAGGGGAGGGCTGGTGGGGGTCTGGGCTCAGCTGGCCCAGGCCTCTAAACTG A G lnc-APLP1-2 RNACentral:URS00008BD804 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35890079..35890150 26863196 MeRIP-seq:(Medium) rs1415603820 Functional Loss SNV dbSNP153 33..33 33 - - - 84068 RMVar_ID_84068 Human_SNP_ID_664613976 m1A Human chr19 - 35900404 35900404 35900404 GGGCGCGGGCAGGACGCGTTCGGCCCCCTAAGAGAGTGAGGGACTGAGGATCGAAAGACTCCCGA GGGCGCGGGCAGGACGCGTTCGGCCCCCTAAGCGAGTGAGGGACTGAGGATCGAAAGACTCCCGA T G NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35900402..35900518 26863196 MeRIP-seq:(Medium) rs1203691165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437405 RMVar_hsa_circ_120027,RMVar_hsa_circ_194302 84069 RMVar_ID_84069 Human_SNP_ID_664623895 m1A Human chr19 - 35936533 35936533 35936533 ACAGACTGGGACACGCGGGATGGGGGCACCGCAGCGCAGGCGGGGGCGCAGGGGGGAGGGGCCGC ACAGACTGGGACACGCGGGATGGGGGCACCGCGGCGCAGGCGGGGGCGCAGGGGGGAGGGGCCGC T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:35936401..35936650 26863410 MeRIP-seq:(Medium) rs1312192481 Functional Loss SNV dbSNP153 33..33 33 - - - 84070 RMVar_ID_84070 Human_SNP_ID_664623913 m1A Human chr19 - 35936613 35936613 35936613 ACCGGCTGCGGTGGGGAGGGGGGCGACCGGGCAGCCCCAGGGCCGGGTGGGGCGAGGCCTGGGAG ACCGGCTGCGGTGGGGAGGGGGGCGACCGGGCCGCCCCAGGGCCGGGTGGGGCGAGGCCTGGGAG T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35936453..35936741 26863196 MeRIP-seq:(Medium) rs1484258422 Functional Loss SNV dbSNP153 33..33 33 - - - 84071 RMVar_ID_84071 Human_SNP_ID_664623947 m1A Human chr19 + 35936709 35936709 35936709 CCAGGAAGCCAGCCGGGACGCCGCCGCCCCGGACCCCGCGCCCTAACCTCCACCTCGGGGGCCTG CCAGGAAGCCAGCCGGGACGCCGCCGCCCCGGGCCCCGCGCCCTAACCTCCACCTCGGGGGCCTG A G LRFN3 Ensembl:ENSG00000126243 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35936659..35936743 26863196 MeRIP-seq:(Medium) rs1232876213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557463 Human_Splice_Rec_1997158 84072 RMVar_ID_84072 Human_SNP_ID_664624559 m1A Human chr19 + 35939506 35939506 35939506 TCATCCCCACCCCAGTCAGCCACACCCAGCCCATGTCCCCGCCGCTGCCGCTGCCAGACACAGTC TCATCCCCACCCCAGTCAGCCACACCCAGCCCGTGTCCCCGCCGCTGCCGCTGCCAGACACAGTC A G LRFN3 Ensembl:ENSG00000126243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:35939469..35939548 26863196 MeRIP-seq:(Medium) rs750737092 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_241493,Human_RBP_ID_18946780 Human_Splice_Rec_1997162,Human_Splice_Rec_1997168 Human_miRNA_ID_1358483 84073 RMVar_ID_84073 Human_SNP_ID_664625770 m1A Human chr19 + 35943613 35943613 35943613 ATTTGGCATAGGCTGCAGGAAATAGGGGAACCAGAGGGAAATTGGCAAGCGTCTGGAGGAGACTG ATTTGGCATAGGCTGCAGGAAATAGGGGAACCGGAGGGAAATTGGCAAGCGTCTGGAGGAGACTG A G LRFN3 Ensembl:ENSG00000126243 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:35943575..35943735 26863196 MeRIP-seq:(Medium) rs916141303 Functional Loss SNV dbSNP153 33..33 33 - - - 84074 RMVar_ID_84074 Human_SNP_ID_664625803 m1A Human chr19 - 35943765 35943764 35943765 CCCAATCCTCTGCCTGATTTCACTCTGGTCCCACTGCCAGTCATCTCTCCAGTTCACCACCCAAT CCCAATCCTCTGCCTGATTTCACTCTGGTCCC_CTGCCAGTCATCTCTCCAGTTCACCACCCAAT GT G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35943464..35943845 26863196 MeRIP-seq:(Medium) rs147375991 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_437 84075 RMVar_ID_84075 Human_SNP_ID_664625918 m1A Human chr19 - 35944278 35944278 35944278 CGTCCTCATAGCCTGCTGCCCATTTTCACTCTAGTCCCACCACCCAATTTCTCTAACAGCTCACC CGTCCTCATAGCCTGCTGCCCATTTTCACTCTCGTCCCACCACCCAATTTCTCTAACAGCTCACC T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:35944232..35944431 26863196 MeRIP-seq:(Medium) rs1391824344 Functional Loss SNV dbSNP153 33..33 33 - - - 84076 RMVar_ID_84076 Human_SNP_ID_664639382 m1A Human chr19 + 35995278 35995278 35995278 TCGCTGAGCGTCTCTGCTTAGCCGCGGTCATGAGCCGGCACAGCCGGCTGCAGAGGCAGGTTCTG TCGCTGAGCGTCTCTGCTTAGCCGCGGTCATGCGCCGGCACAGCCGGCTGCAGAGGCAGGTTCTG A C SDHAF1 Ensembl:ENSG00000205138 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35995232..35995312 26863196 MeRIP-seq:(Medium) rs863224198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558380,Human_RBP_ID_8942209,Human_RBP_ID_18421358 84077 RMVar_ID_84077 Human_SNP_ID_664639383 m1A Human chr19 + 35995278 35995278 35995278 TCGCTGAGCGTCTCTGCTTAGCCGCGGTCATGAGCCGGCACAGCCGGCTGCAGAGGCAGGTTCTG TCGCTGAGCGTCTCTGCTTAGCCGCGGTCATGGGCCGGCACAGCCGGCTGCAGAGGCAGGTTCTG A G SDHAF1 Ensembl:ENSG00000205138 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35995232..35995312 26863196 MeRIP-seq:(Medium) rs863224198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558380,Human_RBP_ID_8942209,Human_RBP_ID_18421358 84078 RMVar_ID_84078 Human_SNP_ID_664641422 m1A Human chr19 + 36003438 36003438 36003438 GCAGCAGGGGCCTCCTGACGCGGGCAGGAGAAACATGGCACCCACCAGGAGGAGGAAGAGGAGGA GCAGCAGGGGCCTCCTGACGCGGGCAGGAGAAGCATGGCACCCACCAGGAGGAGGAAGAGGAGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36003387..36003493 26863196 MeRIP-seq:(Medium) rs1461316920 Functional Loss SNV dbSNP153 33..33 33 - - - 84079 RMVar_ID_84079 Human_SNP_ID_664643614 m1A Human chr19 - 36010679 36010677 36010680 CTGCCCAGCCCTGGTGCCCACTCCCTAGCCCCACGAGGACGGACCACTGTACTACCCGACTGTCA CTGCCCAGCCCTGGTGCCCACTCCCTAGCCC___GAGGACGGACCACTGTACTACCCGACTGTCA CGTG C AC002116.1,ALKBH6 Ensembl:ENSG00000248101,Ensembl:ENSG00000239382 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36010654..36010805 26863196 MeRIP-seq:(Medium) rs1568534645 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_139119,Human_RBP_ID_911267,Human_RBP_ID_5088893,Human_RBP_ID_5586894,Human_RBP_ID_5651238,Human_RBP_ID_17082427,Human_RBP_ID_22066745 Human_Splice_Rec_1997262,Human_Splice_Rec_1997272,Human_Splice_Rec_1997284,Human_Splice_Rec_1997310,Human_Splice_Rec_1997338,Human_Splice_Rec_1997348 84080 RMVar_ID_84080 Human_SNP_ID_664643616 m1A Human chr19 - 36010679 36010679 36010679 CTGCCCAGCCCTGGTGCCCACTCCCTAGCCCCACGAGGACGGACCACTGTACTACCCGACTGTCA CTGCCCAGCCCTGGTGCCCACTCCCTAGCCCCCCGAGGACGGACCACTGTACTACCCGACTGTCA T G AC002116.1,ALKBH6 Ensembl:ENSG00000248101,Ensembl:ENSG00000239382 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36010654..36010805 26863196 MeRIP-seq:(Medium) rs565721671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139119,Human_RBP_ID_911267,Human_RBP_ID_5088893,Human_RBP_ID_5586894,Human_RBP_ID_5651238,Human_RBP_ID_17082427,Human_RBP_ID_22066745 Human_Splice_Rec_1997262,Human_Splice_Rec_1997272,Human_Splice_Rec_1997284,Human_Splice_Rec_1997310,Human_Splice_Rec_1997338,Human_Splice_Rec_1997348 84081 RMVar_ID_84081 Human_SNP_ID_664643651 m1A Human chr19 + 36010824 36010824 36010824 GAGATGTGGCTGCCTAATGAGTGAGGGTGGGTACAGAGTCCCCTGCCCCAGCACAGCTCAGAAGT GAGATGTGGCTGCCTAATGAGTGAGGGTGGGTGCAGAGTCCCCTGCCCCAGCACAGCTCAGAAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36010820..36010905 26863196 MeRIP-seq:(Medium) rs1350098441 Functional Loss SNV dbSNP153 33..33 33 - - - 84082 RMVar_ID_84082 Human_SNP_ID_664650094 m1A Human chr19 + 36035675 36035675 36035675 GAGAGACAGACAGATAACGGTGAGGAACAGGGAGGCAAAGGTGGCAGGAGGGCGTGTCAGGAAAC GAGAGACAGACAGATAACGGTGAGGAACAGGGCGGCAAAGGTGGCAGGAGGGCGTGTCAGGAAAC A C AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36035639..36035741 26863196 MeRIP-seq:(Medium) rs528841714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249134 84083 RMVar_ID_84083 Human_SNP_ID_664655328 m1A Human chr19 + 36054972 36054972 36054972 GGATGTAACGGTCGCCCGCCTCCGGCGTGACGATGGCGGCCGTAGGGTCCGGAGGCTATGCGCGG GGATGTAACGGTCGCCCGCCTCCGGCGTGACGGTGGCGGCCGTAGGGTCCGGAGGCTATGCGCGG A G WDR62 Ensembl:ENSG00000075702 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36054922..36055076 26863196 MeRIP-seq:(Medium) rs1421840721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6747374,Human_RBP_ID_9293630,Human_RBP_ID_18421361 RMVar_hsa_circ_94904,RMVar_hsa_circ_194315,RMVar_hsa_circ_78063,RMVar_hsa_circ_194314 84084 RMVar_ID_84084 Human_SNP_ID_664663541 m1A Human chr19 - 36083591 36083591 36083591 TATCCCACCCTCATAGCCCCTCTCCCAGAGCCACCAGGACCCTCCTCCAGCTGGCATCTTCGGTG TATCCCACCCTCATAGCCCCTCTCCCAGAGCCTCCAGGACCCTCCTCCAGCTGGCATCTTCGGTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:36083586..36083687 26863196 MeRIP-seq:(Medium) rs886543378 Functional Loss SNV dbSNP153 33..33 33 - - - 84085 RMVar_ID_84085 Human_SNP_ID_664669143 m1A Human chr19 - 36103195 36103195 36103195 TCTGGGACTGGGGCACTCACGTGGTGGGCGCCAGGCCTCCAGGGTCTCTTCAGCCTTCCCTGCAG TCTGGGACTGGGGCACTCACGTGGTGGGCGCCTGGCCTCCAGGGTCTCTTCAGCCTTCCCTGCAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36103064..36103481 32194978 MeRIP-seq:(Medium) rs778923974 Functional Loss SNV dbSNP153 33..33 33 - - - 84086 RMVar_ID_84086 Human_SNP_ID_664669144 m1A Human chr19 - 36103195 36103195 36103195 TCTGGGACTGGGGCACTCACGTGGTGGGCGCCAGGCCTCCAGGGTCTCTTCAGCCTTCCCTGCAG TCTGGGACTGGGGCACTCACGTGGTGGGCGCCCGGCCTCCAGGGTCTCTTCAGCCTTCCCTGCAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36103064..36103481 32194978 MeRIP-seq:(Medium) rs778923974 Functional Loss SNV dbSNP153 33..33 33 - - - 84087 RMVar_ID_84087 Human_SNP_ID_664669347 m1A Human chr19 + 36103673 36103673 36103673 GACAACACCCAGTTTGGACAGTGAGGGCCAAGAGCCTGCCCTGCGTTCCTGGGGCAACCACGAGG GACAACACCCAGTTTGGACAGTGAGGGCCAAGTGCCTGCCCTGCGTTCCTGGGGCAACCACGAGG A T WDR62 Ensembl:ENSG00000075702 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36103629..36103929 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1884886,Human_RBP_ID_18729648 Human_miRNA_ID_1194949,Human_miRNA_ID_3089185 RMVar_hsa_circ_95975,RMVar_hsa_circ_194325,RMVar_hsa_circ_100446,RMVar_hsa_circ_194331,RMVar_hsa_circ_127227,RMVar_hsa_circ_194343,RMVar_hsa_circ_91392,RMVar_hsa_circ_194350 84088 RMVar_ID_84088 Human_SNP_ID_664669407 m1A Human chr19 + 36103801 36103801 36103801 ATACCCAGCCTGGCGTCACCGTCCCTGCAGTGAGCTTCCCAGCCCCTAGCCCTGTGGAAGAGAGC ATACCCAGCCTGGCGTCACCGTCCCTGCAGTGCGCTTCCCAGCCCCTAGCCCTGTGGAAGAGAGC A C WDR62 Ensembl:ENSG00000075702 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36103751..36103950 26863196 MeRIP-seq:(Medium) rs764653633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23793800 Human_miRNA_ID_1194950,Human_miRNA_ID_1358488 RMVar_hsa_circ_95975,RMVar_hsa_circ_194325,RMVar_hsa_circ_100446,RMVar_hsa_circ_194331,RMVar_hsa_circ_127227,RMVar_hsa_circ_194343,RMVar_hsa_circ_91392,RMVar_hsa_circ_194350 84089 RMVar_ID_84089 Human_SNP_ID_664669457 m1A Human chr19 - 36103890 36103878 36103891 AGCTGGGGGTTACTGGGGTGGGCAGGAAGGCCAGGGGACTCAGGAGCTGGGAGACTTGGGCGAAA AGCTGGGGGTTACTGGGGTGGGCAGGAAGGC_____________AGCTGGGAGACTTGGGCGAAA TCCTGAGTCCCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36103840..36103917 26863196 MeRIP-seq:(Medium) rs1167066971 Functional Loss DEL dbSNP153 32..44 33 - - - 84090 RMVar_ID_84090 Human_SNP_ID_664669795 m1A Human chr19 + 36104856 36104856 36104856 CTCCACCTTCCTGTGGATCCACAGCCAGCTGGAGGCTGAATGCCTGGTGGGGACTAGTGTGGCCC CTCCACCTTCCTGTGGATCCACAGCCAGCTGGGGGCTGAATGCCTGGTGGGGACTAGTGTGGCCC A G WDR62 Ensembl:ENSG00000075702 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36104806..36105056 32194978 MeRIP-seq:(Medium) rs1184558830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1561605,Human_RBP_ID_18729654 Human_Splice_Rec_1997584,Human_Splice_Rec_1997644,Human_Splice_Rec_1997704 84091 RMVar_ID_84091 Human_SNP_ID_664672654 m1A Human chr19 - 36114180 36114180 36114180 CACGTTGCCGCGGACCGAGGACCACCCGTGCCAAAAGTGAGCGTTCAGCTGGTACTGGGGAGGTA CACGTTGCCGCGGACCGAGGACCACCCGTGCCGAAAGTGAGCGTTCAGCTGGTACTGGGGAGGTA T C POLR2I Ensembl:ENSG00000105258 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36114176..36114250 32194978 MeRIP-seq:(Medium) rs1207047058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_520377,Human_RBP_ID_770754,Human_RBP_ID_8484770,Human_RBP_ID_8832683,Human_RBP_ID_18729674,Human_RBP_ID_26336197,Human_RBP_ID_26467513,Human_RBP_ID_26815721 Human_Splice_Rec_1997762,Human_Splice_Rec_1997763,Human_Splice_Rec_1997770,Human_Splice_Rec_1997771,Human_Splice_Rec_1997778,Human_Splice_Rec_1997779,Human_Splice_Rec_1997788,Human_Splice_Rec_1997789,Human_Splice_Rec_1997796,Human_Splice_Rec_1997797,Human_Splice_Rec_1997806,Human_Splice_Rec_1997807,Human_Splice_Rec_1997812 Human_miRNA_ID_1987180,Human_miRNA_ID_3123697 RMVar_hsa_circ_101538,RMVar_hsa_circ_123799,RMVar_hsa_circ_105411,RMVar_hsa_circ_194362,RMVar_hsa_circ_194363,RMVar_hsa_circ_194361,RMVar_hsa_circ_297221 84092 RMVar_ID_84092 Human_SNP_ID_664672928 m1A Human chr19 - 36114834 36114829 36114834 GCGCGTCGCCATGGAGCCCGACGGGACTTACGAGCCGGGCTTCGTGGGTATTCGCTTCTGCCAGG GCGCGTCGCCATGGAGCCCGACGGGACTTACG_____GGCTTCGTGGGTATTCGCTTCTGCCAGG CCGGCT C POLR2I Ensembl:ENSG00000105258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:36114701..36114900 26863196 MeRIP-seq:(Medium) rs766955849 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_520383,Human_RBP_ID_1561618,Human_RBP_ID_1884898,Human_RBP_ID_4522622,Human_RBP_ID_5320331,Human_RBP_ID_8832685,Human_RBP_ID_9328909,Human_RBP_ID_17695383,Human_RBP_ID_18729675,Human_RBP_ID_23793813 Human_Splice_Rec_1997757,Human_Splice_Rec_1997775,Human_Splice_Rec_1997783,Human_Splice_Rec_1997793,Human_Splice_Rec_1997801 Human_miRNA_ID_2577642 RMVar_hsa_circ_123799,RMVar_hsa_circ_194363 84093 RMVar_ID_84093 Human_SNP_ID_664672984 m1A Human chr19 + 36114885 36114885 36114885 CCATGGCGACGCGCAGCCCGCGCAGCCCTCCCAGCCTTCCGCGCTTGCTCCGCCGCGCTACAGGT CCATGGCGACGCGCAGCCCGCGCAGCCCTCCCTGCCTTCCGCGCTTGCTCCGCCGCGCTACAGGT A T AD001527.2,TBCB Ensembl:ENSG00000279504,Ensembl:ENSG00000105254 Other,Protein coding exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:36114751..36114925 32194978 MeRIP-seq:(Medium) rs1234067396 Functional Loss SNV dbSNP153 33..33 33 - - - 84094 RMVar_ID_84094 Human_SNP_ID_664673061 m1A Human chr19 - 36115086 36115086 36115086 CTGGCACCAGATCCATACTATTCTGTAAACTGAGGCGGCGATGCCCAAAAATTGGAAGCAATTAC CTGGCACCAGATCCATACTATTCTGTAAACTGGGGCGGCGATGCCCAAAAATTGGAAGCAATTAC T C POLR2I Ensembl:ENSG00000105258 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:36115035..36115135 32194978 MeRIP-seq:(Medium) rs1384233103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4522639,Human_RBP_ID_5499451,Human_RBP_ID_22502482 RMVar_hsa_circ_123799,RMVar_hsa_circ_194363 84095 RMVar_ID_84095 Human_SNP_ID_664673504 m1A Human chr19 + 36116163 36116163 36116163 CAAGAGGATGCGCTCCTGGGCTCCTACCCTGTAGATGACGGCTGCCGCATCCACGTGAGGACTCT CAAGAGGATGCGCTCCTGGGCTCCTACCCTGTTGATGACGGCTGCCGCATCCACGTGAGGACTCT A T TBCB Ensembl:ENSG00000105254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:36116113..36116214 32194978 MeRIP-seq:(Medium) rs924649210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1561629,Human_RBP_ID_19093228,Human_RBP_ID_23793817 Human_Splice_Rec_1997817,Human_Splice_Rec_1997821,Human_Splice_Rec_1997833,Human_Splice_Rec_1997839,Human_Splice_Rec_1997851,Human_Splice_Rec_1997861,Human_Splice_Rec_1997865,Human_Splice_Rec_1997873,Human_Splice_Rec_1997879,Human_Splice_Rec_1997885,Human_Splice_Rec_1997893 RMVar_hsa_circ_103645,RMVar_hsa_circ_106961,RMVar_hsa_circ_2254,RMVar_hsa_circ_109094,RMVar_hsa_circ_194364,RMVar_hsa_circ_194365,RMVar_hsa_circ_86386,RMVar_hsa_circ_194366,RMVar_hsa_circ_194367 84096 RMVar_ID_84096 Human_SNP_ID_664674917 m1A Human chr19 - 36121084 36121084 36121084 ACCGCCCCATGCCCCCATCTGACCCTGACAACACCCAGCCCCCACACCTACCCCTCAACTCCCTC ACCGCCCCATGCCCCCATCTGACCCTGACAACTCCCAGCCCCCACACCTACCCCTCAACTCCCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36121080..36121340 26863196 MeRIP-seq:(Medium) rs1302844356 Functional Loss SNV dbSNP153 33..33 33 - - - 84097 RMVar_ID_84097 Human_SNP_ID_664675105 m1A Human chr19 + 36121578 36121578 36121578 GAAGCGCAGCAAGCTCGGCCGGTACAACGAGGAGGAGCGGGCTCAGCAGGAGGCCGAGGCCGCCC GAAGCGCAGCAAGCTCGGCCGGTACAACGAGGGGGAGCGGGCTCAGCAGGAGGCCGAGGCCGCCC A G TBCB Ensembl:ENSG00000105254 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36121494..36121595 26863196 MeRIP-seq:(Medium) rs745664823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6747642,Human_RBP_ID_18997658,Human_RBP_ID_22447699,Human_RBP_ID_26815732 Human_Splice_Rec_1997824,Human_Splice_Rec_1997836,Human_Splice_Rec_1997842,Human_Splice_Rec_1997854,Human_Splice_Rec_1997855,Human_Splice_Rec_1997868,Human_Splice_Rec_1997882,Human_Splice_Rec_1997888,Human_Splice_Rec_1997898 RMVar_hsa_circ_103645,RMVar_hsa_circ_106961,RMVar_hsa_circ_2254,RMVar_hsa_circ_109094,RMVar_hsa_circ_194364,RMVar_hsa_circ_194365,RMVar_hsa_circ_86386,RMVar_hsa_circ_54005,RMVar_hsa_circ_194366,RMVar_hsa_circ_194367,RMVar_hsa_circ_115472,RMVar_hsa_circ_307621,RMVar_hsa_circ_125659,RMVar_hsa_circ_194368,RMVar_hsa_circ_194369 84098 RMVar_ID_84098 Human_SNP_ID_664675178 m1A Human chr19 - 36121710 36121710 36121710 GGACCGGGCCCGCGAGCCACGCACCTACATACATGACGGTGCCCCGGCGAGGGGATTGTCCCGCC GGACCGGGCCCGCGAGCCACGCACCTACATACGTGACGGTGCCCCGGCGAGGGGATTGTCCCGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:36121551..36121774;chr19:36121526..36121725 32194978 MeRIP-seq:(Medium) rs1269772114 Functional Loss SNV dbSNP153 33..33 33 - - - 84099 RMVar_ID_84099 Human_SNP_ID_664675318 m1A Human chr19 + 36122021 36122021 36122021 AAGCGTGGGGCAGTGTCAGTCGCGGTGGGGAAACGGGCGGCGTGACCAAGGCAGGAGTGAGGGAA AAGCGTGGGGCAGTGTCAGTCGCGGTGGGGAAGCGGGCGGCGTGACCAAGGCAGGAGTGAGGGAA A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36122016..36122155 26863196 MeRIP-seq:(Medium) rs1364993736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103645,RMVar_hsa_circ_2254,RMVar_hsa_circ_109094,RMVar_hsa_circ_194365,RMVar_hsa_circ_54005,RMVar_hsa_circ_194367,RMVar_hsa_circ_115472,RMVar_hsa_circ_194368 84100 RMVar_ID_84100 Human_SNP_ID_664676264 m1A Human chr19 + 36125466 36125466 36125466 TTCTCTTCTGTTGGCAGGTCTCACAGATTTCAAGCCTGGCTACTGGATTGGTGTCCGCTATGATG TTCTCTTCTGTTGGCAGGTCTCACAGATTTCAGGCCTGGCTACTGGATTGGTGTCCGCTATGATG A G TBCB Ensembl:ENSG00000105254 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36125451..36125525 32194978 MeRIP-seq:(Medium) rs967028606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911283,Human_RBP_ID_6747646,Human_RBP_ID_17657004,Human_RBP_ID_17921819,Human_RBP_ID_18729686,Human_RBP_ID_18994892,Human_RBP_ID_22545974,Human_RBP_ID_23793828 Human_Splice_Rec_1997826,Human_Splice_Rec_1997827,Human_Splice_Rec_1997846,Human_Splice_Rec_1997847,Human_Splice_Rec_1997856,Human_Splice_Rec_1997857,Human_Splice_Rec_1997870,Human_Splice_Rec_1997871,Human_Splice_Rec_1997890,Human_Splice_Rec_1997891,Human_Splice_Rec_1997894,Human_Splice_Rec_1997895,Human_Splice_Rec_1997900,Human_Splice_Rec_1997901,Human_Splice_Rec_1997904,Human_Splice_Rec_1997905 RMVar_hsa_circ_103645,RMVar_hsa_circ_79101,RMVar_hsa_circ_2254,RMVar_hsa_circ_109094,RMVar_hsa_circ_194365,RMVar_hsa_circ_54005,RMVar_hsa_circ_194367,RMVar_hsa_circ_115472,RMVar_hsa_circ_194368,RMVar_hsa_circ_194370 84101 RMVar_ID_84101 Human_SNP_ID_664680118 m1A Human chr19 - 36140151 36140140 36140151 GGAGGGGGTACGGGCCGGGCGCTTACCGCCGCACACGTCCGGAGTTCTGGGAGTCGGTTCCACTG GGAGGGGGTACGGGCCGGGCGCTTACCGCCGC___________GTTCTGGGAGTCGGTTCCACTG CTCCGGACGTGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:36140101..36140268 26863196 MeRIP-seq:(Medium) rs1274107901 Functional Loss DEL dbSNP153 33..43 33 - - - 84102 RMVar_ID_84102 Human_SNP_ID_664680123 m1A Human chr19 - 36140159 36140159 36140159 CGGGGTGCGGAGGGGGTACGGGCCGGGCGCTTACCGCCGCACACGTCCGGAGTTCTGGGAGTCGG CGGGGTGCGGAGGGGGTACGGGCCGGGCGCTTGCCGCCGCACACGTCCGGAGTTCTGGGAGTCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEPG2 cell line,total RNA Untreated chr19:36140071..36140250;chr19:36140076..36140265;chr19:36140132..36140254;chr19:36140132..36140227 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1568388994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1239875 84103 RMVar_ID_84103 Human_SNP_ID_664680390 m1A Human chr19 - 36141085 36141085 36141085 CCCCGCTGATCAGGCCTCCAAGCACATTTCCCAGGCCCCCACCCAGGCCCCCGCCTCCCCCGCCG CCCCGCTGATCAGGCCTCCAAGCACATTTCCCGGGCCCCCACCCAGGCCCCCGCCTCCCCCGCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:36140995..36141151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 84104 RMVar_ID_84104 Human_SNP_ID_664680391 m1A Human chr19 - 36141085 36141085 36141085 CCCCGCTGATCAGGCCTCCAAGCACATTTCCCAGGCCCCCACCCAGGCCCCCGCCTCCCCCGCCG CCCCGCTGATCAGGCCTCCAAGCACATTTCCCCGGCCCCCACCCAGGCCCCCGCCTCCCCCGCCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:36140995..36141151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 84105 RMVar_ID_84105 Human_SNP_ID_664680392 m1A Human chr19 - 36141097 36141088 36141097 CGCCGCCCCCGGCCCCGCTGATCAGGCCTCCAAGCACATTTCCCAGGCCCCCACCCAGGCCCCCG CGCCGCCCCCGGCCCCGCTGATCAGGCCTCCA_________CCCAGGCCCCCACCCAGGCCCCCG GAAATGTGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36140964..36141339 26863196 MeRIP-seq:(Medium) rs1317466417 Functional Loss DEL dbSNP153 33..41 33 - - - 84106 RMVar_ID_84106 Human_SNP_ID_664680432 m1A Human chr19 - 36141155 36141137 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACC__________________GCCGCCGCCGCCGCC CGGCGGCGGCGGCGGCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs1288534936 Functional Loss DEL dbSNP153 33..50 33 - - - 84107 RMVar_ID_84107 Human_SNP_ID_664680439 m1A Human chr19 - 36141155 36141143 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACC____________GCCGCCGCCGCCGCCGCCGCC CGGCGGCGGCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs1414461543 Functional Loss DEL dbSNP153 33..44 33 - - - 84108 RMVar_ID_84108 Human_SNP_ID_664680448 m1A Human chr19 - 36141155 36141149 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACC______GCCGCCGCCGCCGCCGCCGCCGCCGCC CGGCGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs758160197 Functional Loss DEL dbSNP153 33..38 33 - - - 84109 RMVar_ID_84109 Human_SNP_ID_664680452 m1A Human chr19 - 36141155 36141152 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACC___GCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs747187044 Functional Loss DEL dbSNP153 33..35 33 - - - 84110 RMVar_ID_84110 Human_SNP_ID_664680457 m1A Human chr19 - 36141155 36141155 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACCTCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs538969591 Functional Loss SNV dbSNP153 33..33 33 - - - 84111 RMVar_ID_84111 Human_SNP_ID_664680458 m1A Human chr19 - 36141155 36141155 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs538969591 Functional Loss SNV dbSNP153 33..33 33 - - - 84112 RMVar_ID_84112 Human_SNP_ID_664680459 m1A Human chr19 - 36141155 36141155 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs538969591 Functional Loss SNV dbSNP153 33..33 33 - - - 84113 RMVar_ID_84113 Human_SNP_ID_664680466 m1A Human chr19 - 36141158 36141158 36141158 CGCATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCATGGCCGTTCCACCGCCACCGCCGCCTCCTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,H2O2 treatment;HEK293T,untreat control chr19:36140976..36141302;chr19:36140976..36141339;chr19:36141001..36141236;chr19:36141058..36141158;chr19:36141046..36141250 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs11084845 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 84114 RMVar_ID_84114 Human_SNP_ID_664680467 m1A Human chr19 - 36141158 36141158 36141158 CGCATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCATGGCCGTTCCACCGCCACCGCCGCCTCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,H2O2 treatment;HEK293T,untreat control chr19:36140976..36141302;chr19:36140976..36141339;chr19:36141001..36141236;chr19:36141058..36141158;chr19:36141046..36141250 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs11084845 Functional Loss SNV dbSNP153 33..33 33 - - - 84115 RMVar_ID_84115 Human_SNP_ID_664680468 m1A Human chr19 - 36141158 36141158 36141158 CGCATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCATGGCCGTTCCACCGCCACCGCCGCCTCCCCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,H2O2 treatment;HEK293T,untreat control chr19:36140976..36141302;chr19:36140976..36141339;chr19:36141001..36141236;chr19:36141058..36141158;chr19:36141046..36141250 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs11084845 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 84116 RMVar_ID_84116 Human_SNP_ID_664680495 m1A Human chr19 + 36141186 36141186 36141186 GTGGTGGAGGCGGCGGTGGCGGTGGAACGGCCATGCGCATCCTAGGCGGAGTCATCAGCGCCATC GTGGTGGAGGCGGCGGTGGCGGTGGAACGGCCGTGCGCATCCTAGGCGGAGTCATCAGCGCCATC A G CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36140976..36141339 26863196 MeRIP-seq:(Medium) rs779024915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53609,Human_RBP_ID_769659,Human_RBP_ID_912599,Human_RBP_ID_4558388,Human_RBP_ID_5117473,Human_RBP_ID_6747669,Human_RBP_ID_9328911,Human_RBP_ID_17656097,Human_RBP_ID_18441163,Human_RBP_ID_22447701,Human_RBP_ID_22502489 Human_Splice_Rec_1997919,Human_Splice_Rec_1997937,Human_Splice_Rec_1997957,Human_Splice_Rec_1997977,Human_Splice_Rec_1997997,Human_Splice_Rec_1998001,Human_Splice_Rec_1998019,Human_Splice_Rec_1998039,Human_Splice_Rec_1998049,Human_Splice_Rec_1998075,Human_Splice_Rec_1998091,Human_Splice_Rec_1998109 RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_97622,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194374,RMVar_hsa_circ_194375,RMVar_hsa_circ_118129,RMVar_hsa_circ_118214,RMVar_hsa_circ_194376,RMVar_hsa_circ_194377,RMVar_hsa_circ_194378 84117 RMVar_ID_84117 Human_SNP_ID_664680500 m1A Human chr19 + 36141192 36141192 36141192 GAGGCGGCGGTGGCGGTGGAACGGCCATGCGCATCCTAGGCGGAGTCATCAGCGCCATCAGGTAA GAGGCGGCGGTGGCGGTGGAACGGCCATGCGCCTCCTAGGCGGAGTCATCAGCGCCATCAGGTAA A C CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:36140976..36141275 26863410 MeRIP-seq:(Medium) rs773120912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769659,Human_RBP_ID_912599,Human_RBP_ID_4558388,Human_RBP_ID_5117473,Human_RBP_ID_6747669,Human_RBP_ID_9330002,Human_RBP_ID_17656097,Human_RBP_ID_18441163,Human_RBP_ID_22447701,Human_RBP_ID_22502489 Human_Splice_Rec_1997919,Human_Splice_Rec_1997937,Human_Splice_Rec_1997957,Human_Splice_Rec_1997977,Human_Splice_Rec_1997997,Human_Splice_Rec_1998001,Human_Splice_Rec_1998019,Human_Splice_Rec_1998039,Human_Splice_Rec_1998049,Human_Splice_Rec_1998075,Human_Splice_Rec_1998091,Human_Splice_Rec_1998109 RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_97622,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194374,RMVar_hsa_circ_194375,RMVar_hsa_circ_118129,RMVar_hsa_circ_118214,RMVar_hsa_circ_194376,RMVar_hsa_circ_194377,RMVar_hsa_circ_194378 84118 RMVar_ID_84118 Human_SNP_ID_664680504 m1A Human chr19 + 36141197 36141197 36141197 GGCGGTGGCGGTGGAACGGCCATGCGCATCCTAGGCGGAGTCATCAGCGCCATCAGGTAAGGCGG GGCGGTGGCGGTGGAACGGCCATGCGCATCCTTGGCGGAGTCATCAGCGCCATCAGGTAAGGCGG A T CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:36141176..36141200 26863196 MeRIP-seq:(Medium) rs1281448157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769659,Human_RBP_ID_912599,Human_RBP_ID_4558388,Human_RBP_ID_5117473,Human_RBP_ID_6747669,Human_RBP_ID_9330002,Human_RBP_ID_17656097,Human_RBP_ID_18441163,Human_RBP_ID_22447701,Human_RBP_ID_22502489 Human_Splice_Rec_1997919,Human_Splice_Rec_1997937,Human_Splice_Rec_1997957,Human_Splice_Rec_1997977,Human_Splice_Rec_1997997,Human_Splice_Rec_1998001,Human_Splice_Rec_1998019,Human_Splice_Rec_1998039,Human_Splice_Rec_1998049,Human_Splice_Rec_1998075,Human_Splice_Rec_1998091,Human_Splice_Rec_1998109 RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_97622,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194374,RMVar_hsa_circ_194375,RMVar_hsa_circ_118129,RMVar_hsa_circ_118214,RMVar_hsa_circ_194376,RMVar_hsa_circ_194377,RMVar_hsa_circ_194378 84119 RMVar_ID_84119 Human_SNP_ID_664680914 m1A Human chr19 - 36142592 36142592 36142592 GGGGAGGGGAACCCGGCCAGGACGGCTCCCCAAACCCAGGTACCCTGGGTGGGGAAGTCAGAGTG GGGGAGGGGAACCCGGCCAGGACGGCTCCCCAGACCCAGGTACCCTGGGTGGGGAAGTCAGAGTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:36142588..36142890 26863410 MeRIP-seq:(Medium) rs1382366572 Functional Loss SNV dbSNP153 33..33 33 - - - 84120 RMVar_ID_84120 Human_SNP_ID_664680915 m1A Human chr19 - 36142592 36142592 36142592 GGGGAGGGGAACCCGGCCAGGACGGCTCCCCAAACCCAGGTACCCTGGGTGGGGAAGTCAGAGTG GGGGAGGGGAACCCGGCCAGGACGGCTCCCCACACCCAGGTACCCTGGGTGGGGAAGTCAGAGTG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:36142588..36142890 26863410 MeRIP-seq:(Medium) rs1382366572 Functional Loss SNV dbSNP153 33..33 33 - - - 84121 RMVar_ID_84121 Human_SNP_ID_664680918 m1A Human chr19 - 36142603 36142603 36142603 GCTCAGAGCAGGGGGAGGGGAACCCGGCCAGGACGGCTCCCCAAACCCAGGTACCCTGGGTGGGG GCTCAGAGCAGGGGGAGGGGAACCCGGCCAGGGCGGCTCCCCAAACCCAGGTACCCTGGGTGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36142598..36142772 26863196 MeRIP-seq:(Medium) rs1001134137 Functional Loss SNV dbSNP153 33..33 33 - - - 84122 RMVar_ID_84122 Human_SNP_ID_664680950 m1A Human chr19 + 36142657 36142657 36142657 CTGCTCTGAGCTCTCCTCCCTTTGCAGCCCCCACGCACACATTACTCCAACATTGAGGCCAACGA CTGCTCTGAGCTCTCCTCCCTTTGCAGCCCCCGCGCACACATTACTCCAACATTGAGGCCAACGA A G CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:36142651..36142725 26863196 MeRIP-seq:(Medium) rs116114216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825114,Human_RBP_ID_17921829,Human_RBP_ID_23210938,Human_RBP_ID_26817439 Human_Splice_Rec_1997940,Human_Splice_Rec_1997941,Human_Splice_Rec_1997960,Human_Splice_Rec_1997961,Human_Splice_Rec_1997980,Human_Splice_Rec_1997981,Human_Splice_Rec_1998022,Human_Splice_Rec_1998023,Human_Splice_Rec_1998042,Human_Splice_Rec_1998043,Human_Splice_Rec_1998052,Human_Splice_Rec_1998053,Human_Splice_Rec_1998078,Human_Splice_Rec_1998079,Human_Splice_Rec_1998094,Human_Splice_Rec_1998095,Human_Splice_Rec_1998112,Human_Splice_Rec_1998116,Human_Splice_Rec_1998117,Human_Splice_Rec_1998130,Human_Splice_Rec_1998131 Human_miRNA_ID_2206059,Human_miRNA_ID_2206060 RMVar_hsa_circ_82142,RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_97622,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194374,RMVar_hsa_circ_194375,RMVar_hsa_circ_118129,RMVar_hsa_circ_97348,RMVar_hsa_circ_118214,RMVar_hsa_circ_194376,RMVar_hsa_circ_194377,RMVar_hsa_circ_99443,RMVar_hsa_circ_194378,RMVar_hsa_circ_93918,RMVar_hsa_circ_83183,RMVar_hsa_circ_117523,RMVar_hsa_circ_194379,RMVar_hsa_circ_194381,RMVar_hsa_circ_194382,RMVar_hsa_circ_194380,RMVar_hsa_circ_126124,RMVar_hsa_circ_372891,RMVar_hsa_circ_113563,RMVar_hsa_circ_194384,RMVar_hsa_circ_194386,RMVar_hsa_circ_194387,RMVar_hsa_circ_194385,RMVar_hsa_circ_194383 84123 RMVar_ID_84123 Human_SNP_ID_664681035 m1A Human chr19 + 36142912 36142912 36142912 CCTGACCTGCCCCTAACTTCCGCCCGCAGGACATGGAGGTCAGCGCCACAGAACTCATGAACATT CCTGACCTGCCCCTAACTTCCGCCCGCAGGACCTGGAGGTCAGCGCCACAGAACTCATGAACATT A C CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:36142901..36142925 32194978 MeRIP-seq:(Medium) rs1354142497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825115,Human_RBP_ID_911285,Human_RBP_ID_1188970,Human_RBP_ID_3954949,Human_RBP_ID_8484798,Human_RBP_ID_17921830,Human_RBP_ID_18994893,Human_RBP_ID_22448646 Human_Splice_Rec_1997922,Human_Splice_Rec_1997923,Human_Splice_Rec_1997942,Human_Splice_Rec_1997943,Human_Splice_Rec_1997962,Human_Splice_Rec_1997963,Human_Splice_Rec_1997982,Human_Splice_Rec_1997983,Human_Splice_Rec_1998004,Human_Splice_Rec_1998005,Human_Splice_Rec_1998024,Human_Splice_Rec_1998025,Human_Splice_Rec_1998044,Human_Splice_Rec_1998045,Human_Splice_Rec_1998054,Human_Splice_Rec_1998055,Human_Splice_Rec_1998080,Human_Splice_Rec_1998081,Human_Splice_Rec_1998096,Human_Splice_Rec_1998097,Human_Splice_Rec_1998118,Human_Splice_Rec_1998119,Human_Splice_Rec_1998132,Human_Splice_Rec_1998133 RMVar_hsa_circ_82142,RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194375,RMVar_hsa_circ_118129,RMVar_hsa_circ_97348,RMVar_hsa_circ_118214,RMVar_hsa_circ_194376,RMVar_hsa_circ_194377,RMVar_hsa_circ_99443,RMVar_hsa_circ_194378,RMVar_hsa_circ_93918,RMVar_hsa_circ_122560,RMVar_hsa_circ_83183,RMVar_hsa_circ_117523,RMVar_hsa_circ_194379,RMVar_hsa_circ_194381,RMVar_hsa_circ_194382,RMVar_hsa_circ_194380,RMVar_hsa_circ_126124,RMVar_hsa_circ_113563,RMVar_hsa_circ_194384,RMVar_hsa_circ_194386,RMVar_hsa_circ_194387,RMVar_hsa_circ_194385,RMVar_hsa_circ_194388,RMVar_hsa_circ_77612,RMVar_hsa_circ_94745,RMVar_hsa_circ_194389,RMVar_hsa_circ_194390 84124 RMVar_ID_84124 Human_SNP_ID_664681088 m1A Human chr19 + 36143078 36143078 36143078 TCAACCTGTTACCCACAGACCCTGATCTGAAGACTGATGGTTTTGGCATTGACACATGTCGCAGC TCAACCTGTTACCCACAGACCCTGATCTGAAGGCTGATGGTTTTGGCATTGACACATGTCGCAGC A G CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36142862..36143180 26863196 MeRIP-seq:(Medium) rs778193447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53611,Human_RBP_ID_1561644,Human_RBP_ID_1884910,Human_RBP_ID_5190640,Human_RBP_ID_5370319,Human_RBP_ID_9086921,Human_RBP_ID_13438845,Human_RBP_ID_22665342,Human_RBP_ID_22762935,Human_RBP_ID_23793843 Human_Splice_Rec_1997924,Human_Splice_Rec_1997925,Human_Splice_Rec_1997944,Human_Splice_Rec_1997945,Human_Splice_Rec_1997964,Human_Splice_Rec_1997965,Human_Splice_Rec_1997984,Human_Splice_Rec_1997985,Human_Splice_Rec_1998006,Human_Splice_Rec_1998007,Human_Splice_Rec_1998026,Human_Splice_Rec_1998027,Human_Splice_Rec_1998046,Human_Splice_Rec_1998047,Human_Splice_Rec_1998056,Human_Splice_Rec_1998057,Human_Splice_Rec_1998082,Human_Splice_Rec_1998083,Human_Splice_Rec_1998098,Human_Splice_Rec_1998099,Human_Splice_Rec_1998120,Human_Splice_Rec_1998121,Human_Splice_Rec_1998134,Human_Splice_Rec_1998135 RMVar_hsa_circ_82142,RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194375,RMVar_hsa_circ_97348,RMVar_hsa_circ_118214,RMVar_hsa_circ_194377,RMVar_hsa_circ_99443,RMVar_hsa_circ_194378,RMVar_hsa_circ_122560,RMVar_hsa_circ_117523,RMVar_hsa_circ_194379,RMVar_hsa_circ_194381,RMVar_hsa_circ_194380,RMVar_hsa_circ_126124,RMVar_hsa_circ_113563,RMVar_hsa_circ_194386,RMVar_hsa_circ_194387,RMVar_hsa_circ_194385,RMVar_hsa_circ_194388,RMVar_hsa_circ_77612,RMVar_hsa_circ_94745,RMVar_hsa_circ_194389,RMVar_hsa_circ_194390,RMVar_hsa_circ_90264,RMVar_hsa_circ_112986,RMVar_hsa_circ_194391,RMVar_hsa_circ_194392 84125 RMVar_ID_84125 Human_SNP_ID_664681818 m1A Human chr19 + 36145760 36145760 36145760 TATCACCATCGTGTCCACAGTGCATGTGATGCATGCATCTGGGTGTAGCTGTCACTCTTCTTAAC TATCACCATCGTGTCCACAGTGCATGTGATGCGTGCATCTGGGTGTAGCTGTCACTCTTCTTAAC A G CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:36145756..36145991 26863196 MeRIP-seq:(Medium) rs913717710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82142,RMVar_hsa_circ_92302,RMVar_hsa_circ_80600,RMVar_hsa_circ_126013,RMVar_hsa_circ_194372,RMVar_hsa_circ_194373,RMVar_hsa_circ_101323,RMVar_hsa_circ_194375,RMVar_hsa_circ_97348,RMVar_hsa_circ_118214,RMVar_hsa_circ_194377,RMVar_hsa_circ_99443,RMVar_hsa_circ_194378,RMVar_hsa_circ_122560,RMVar_hsa_circ_117523,RMVar_hsa_circ_194379,RMVar_hsa_circ_194381,RMVar_hsa_circ_194380,RMVar_hsa_circ_113563,RMVar_hsa_circ_194386,RMVar_hsa_circ_194387,RMVar_hsa_circ_194388,RMVar_hsa_circ_77612,RMVar_hsa_circ_94745,RMVar_hsa_circ_194389,RMVar_hsa_circ_194390,RMVar_hsa_circ_90264,RMVar_hsa_circ_112986,RMVar_hsa_circ_194391,RMVar_hsa_circ_194392 84126 RMVar_ID_84126 Human_SNP_ID_664681852 m1A Human chr19 - 36145876 36145876 36145876 CTGGGTGCCAGGGATTTCAGAGGTTTCTACACACCTGCCACCTTTTGATGTTGTTCCACAAGTAC CTGGGTGCCAGGGATTTCAGAGGTTTCTACACGCCTGCCACCTTTTGATGTTGTTCCACAAGTAC T C AD001527.1 Ensembl:ENSG00000270760 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36145866..36145964 26863196 MeRIP-seq:(Medium) rs112192701 Functional Loss SNV dbSNP153 33..33 33 - - - 84127 RMVar_ID_84127 Human_SNP_ID_664683048 m1A Human chr19 - 36150120 36150119 36150120 GGCATCACAAGTGCTAGGCTTGGCACAGGTACAGGGGAGAGGTTACGGAGTGGGTGTGTGCAGGG GGCATCACAAGTGCTAGGCTTGGCACAGGTAC_GGGGAGAGGTTACGGAGTGGGTGTGTGCAGGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:36149957..36150269 26863196 MeRIP-seq:(Medium) rs1367503237 Functional Loss DEL dbSNP153 33..33 33 - - - 84128 RMVar_ID_84128 Human_SNP_ID_664683085 m1A Human chr19 - 36150284 36150284 36150284 GGCCTGGCAGGCTGGGAGCAGAATATAGACAAAGGCACTGGGGCACCTGGGTCTGGCACGGTCTG GGCCTGGCAGGCTGGGAGCAGAATATAGACAAGGGCACTGGGGCACCTGGGTCTGGCACGGTCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:36149801..36150350 32194978 MeRIP-seq:(Medium) rs1402494310 Functional Loss SNV dbSNP153 33..33 33 - - - 84129 RMVar_ID_84129 Human_SNP_ID_664685213 m1A Human chr19 - 36157232 36157232 36157232 ATGACTGCATCTCTGTGATCCACCTGATGTTCATCCCATTTCCCCACATTTCCTTCTTCCCTGTT ATGACTGCATCTCTGTGATCCACCTGATGTTCTTCCCATTTCCCCACATTTCCTTCTTCCCTGTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:36157213..36157311 26863196 MeRIP-seq:(Medium) rs896289919 Functional Loss SNV dbSNP153 33..33 33 - - - 84130 RMVar_ID_84130 Human_SNP_ID_664685214 m1A Human chr19 - 36157232 36157232 36157232 ATGACTGCATCTCTGTGATCCACCTGATGTTCATCCCATTTCCCCACATTTCCTTCTTCCCTGTT ATGACTGCATCTCTGTGATCCACCTGATGTTCGTCCCATTTCCCCACATTTCCTTCTTCCCTGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:36157213..36157311 26863196 MeRIP-seq:(Medium) rs896289919 Functional Loss SNV dbSNP153 33..33 33 - - - 84131 RMVar_ID_84131 Human_SNP_ID_664685222 m1A Human chr19 + 36157255 36157255 36157255 GAAATGGGATGAACATCAGGTGGATCACAGAGATGCAGTCATGGGGGTCAGGTGTGGTATCCGGA GAAATGGGATGAACATCAGGTGGATCACAGAGTTGCAGTCATGGGGGTCAGGTGTGGTATCCGGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36157231..36157317 26863196 MeRIP-seq:(Medium) rs1380932533 Functional Loss SNV dbSNP153 33..33 33 - - - 84132 RMVar_ID_84132 Human_SNP_ID_664686355 m1A Human chr19 + 36160781 36160776 36160782 AAATTACAGTCAAAGGGGGTTCTCTGGTGGGCAGGGGCAGGGGGTCACAAAGTGCTCAGTGGGGG AAATTACAGTCAAAGGGGGTTCTCTGGT______GGGCAGGGGGTCACAAAGTGCTCAGTGGGGG TGGGCAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36160762..36160827 26863196 MeRIP-seq:(Medium) rs1005389387 Functional Loss DEL dbSNP153 29..34 33 - - - 84133 RMVar_ID_84133 Human_SNP_ID_664700928 m1A Human chr19 + 36213902 36213902 36213902 AGTCACAATCACACACCCGCTAAGACACACCCAGTCACACAATCTACTCTCCACTGTGATACAGT AGTCACAATCACACACCCGCTAAGACACACCCGGTCACACAATCTACTCTCCACTGTGATACAGT A G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36213851..36213980 26863196 MeRIP-seq:(Medium) rs777953156 Functional Loss SNV dbSNP153 33..33 33 - - - 84134 RMVar_ID_84134 Human_SNP_ID_664705441 m1A Human chr19 + 36230433 36230433 36230433 ACTTAAAAAATGTATACTATCAGATAGTGATAAGTGCTATGGAAAAGAATAAAGTAAGGGAAAAC ACTTAAAAAATGTATACTATCAGATAGTGATACGTGCTATGGAAAAGAATAAAGTAAGGGAAAAC A C ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36230430..36230591 26863196 MeRIP-seq:(Medium) rs376908897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1885028,Human_RBP_ID_3569118,Human_RBP_ID_9917560 84135 RMVar_ID_84135 Human_SNP_ID_664706907 m1A Human chr19 - 36235678 36235678 36235678 CCTCTCAAGTCCTGGTGCCTCTCTATCTGTGCATCATCTTCTCAGGCTTCTTCTAAAATGGAGTA CCTCTCAAGTCCTGGTGCCTCTCTATCTGTGCCTCATCTTCTCAGGCTTCTTCTAAAATGGAGTA T G ZNF565 Ensembl:ENSG00000196357 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:36235651..36235700 26863196 MeRIP-seq:(Medium) rs1419431439 Functional Loss SNV dbSNP153 33..33 33 - - - 84136 RMVar_ID_84136 Human_SNP_ID_664729796 m1A Human chr19 - 36331625 36331625 36331625 CGTGCCTGCCGGACATGGGACGCTGGAGGGTCAGCAGCGTGGAGTCCTGGCCTTTTGCGTCCACG CGTGCCTGCCGGACATGGGACGCTGGAGGGTCGGCAGCGTGGAGTCCTGGCCTTTTGCGTCCACG T C LINC00665 Ensembl:ENSG00000232677 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:36331528..36331725 26863196 MeRIP-seq:(Medium) rs1265356016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1133452,Human_RBP_ID_1562149,Human_RBP_ID_4567167,Human_RBP_ID_6748896,Human_RBP_ID_8257149,Human_RBP_ID_23278131 84137 RMVar_ID_84137 Human_SNP_ID_664768697 m1A Human chr19 + 36489707 36489707 36489707 TGTCCGCGCCTTGCGTCAGCCCCGCCGAAAGGATCGCCCCCCCTAGTCAAACCGCTCGCGCCCCA TGTCCGCGCCTTGCGTCAGCCCCGCCGAAAGGGTCGCCCCCCCTAGTCAAACCGCTCGCGCCCCA A G AC092295.2 Ensembl:ENSG00000267309 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:36489663..36489798 26863196 MeRIP-seq:(Medium) rs1357205031 Functional Loss SNV dbSNP153 33..33 33 - - - 84138 RMVar_ID_84138 Human_SNP_ID_664966963 m1A Human chr19 + 37317985 37317985 37317985 TCCGCAGTCTTGGGCTGTTCGGCCAAGCGCCCACCGGACGTGGGACGCTGGAGGGTCAGCAGCGT TCCGCAGTCTTGGGCTGTTCGGCCAAGCGCCCGCCGGACGTGGGACGCTGGAGGGTCAGCAGCGT A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:37317938..37318055 26863196 MeRIP-seq:(Medium) rs1422229793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420920 RMVar_hsa_circ_96977,RMVar_hsa_circ_194473 84139 RMVar_ID_84139 Human_SNP_ID_664979181 m1A Human chr19 - 37363698 37363698 37363698 ACTAAAGCCCCGTCCACACTTTCTGCAAATATAAGGCTTCTCTCCTGAATGTGTCCTCTGGTGTC ACTAAAGCCCCGTCCACACTTTCTGCAAATATGAGGCTTCTCTCCTGAATGTGTCCTCTGGTGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:37363648..37363897 32194978 MeRIP-seq:(Medium) rs1464313970 Functional Loss SNV dbSNP153 33..33 33 - - - 84140 RMVar_ID_84140 Human_SNP_ID_665048105 m1A Human chr19 + 37655406 37655406 37655406 AAAAGCAGCGGCCACAGTGGCGCCCGGCTCCCAGCCCCAGCCTCACCCGACTCAGAGGATAGCCC AAAAGCAGCGGCCACAGTGGCGCCCGGCTCCCGGCCCCAGCCTCACCCGACTCAGAGGATAGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:37655221..37655418;chr19:37655300..37655420 26863196 MeRIP-seq:(Medium) rs1288217461 Functional Loss SNV dbSNP153 33..33 33 - - - 84141 RMVar_ID_84141 Human_SNP_ID_665075408 m1A Human chr19 - 37768368 37768368 37768368 AGAGAGAGCTATGTGAGTTTGAGGAGCACCAAAGTAGACCAGAATAGAGATCCTAAGAGGAGAGT AGAGAGAGCTATGTGAGTTTGAGGAGCACCAACGTAGACCAGAATAGAGATCCTAAGAGGAGAGT T G ZNF573 Ensembl:ENSG00000189144 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:37768319..37768496 26863196 MeRIP-seq:(Medium) rs1306518846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13447118 RMVar_hsa_circ_43629 84142 RMVar_ID_84142 Human_SNP_ID_665081283 m1A Human chr19 + 37792613 37792613 37792613 TATCCATCTCAGATACCAGCAACTCCCCCATCATATGAATCTGTAGATGACATTAATGCTGATAA TATCCATCTCAGATACCAGCAACTCCCCCATCGTATGAATCTGTAGATGACATTAATGCTGATAA A G AC016582.2 Ensembl:ENSG00000267422 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879202738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23796028 84143 RMVar_ID_84143 Human_SNP_ID_665108693 m1A Human chr19 - 37907290 37907290 37907290 ATCGCGGCGTCCAGCTCCGCGCCGCTCGCTGGAGACGCCGCCAGCTCCGGTGGCCCGAGTGACTT ATCGCGGCGTCCAGCTCCGCGCCGCTCGCTGGGGACGCCGCCAGCTCCGGTGGCCCGAGTGACTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:37907241..37907411 26863196 MeRIP-seq:(Medium) rs921589751 Functional Loss SNV dbSNP153 33..33 33 - - - 84144 RMVar_ID_84144 Human_SNP_ID_665117444 m1A Human chr19 + 37942242 37942235 37942243 GGGACACAGTCAAGGAAGAAGTAAACAGATTAATAAGATAATTCCAGATGGGGATGAATAATGCT GGGACACAGTCAAGGAAGAAGTAAAC________AAGATAATTCCAGATGGGGATGAATAATGCT CAGATTAAT C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:37942240..37942473 26863196 MeRIP-seq:(Medium) rs1166561573 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 84145 RMVar_ID_84145 Human_SNP_ID_665117445 m1A Human chr19 + 37942242 37942242 37942242 GGGACACAGTCAAGGAAGAAGTAAACAGATTAATAAGATAATTCCAGATGGGGATGAATAATGCT GGGACACAGTCAAGGAAGAAGTAAACAGATTATTAAGATAATTCCAGATGGGGATGAATAATGCT A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:37942240..37942473 26863196 MeRIP-seq:(Medium) rs916840089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 84146 RMVar_ID_84146 Human_SNP_ID_665117540 m1A Human chr19 + 37942566 37942566 37942566 AGGGGGAGGGCAGGAGACGGGGGTGGCGGGGGAGCCTGGTGAGGGTGTGGGTTTGATTCAGAGTG AGGGGGAGGGCAGGAGACGGGGGTGGCGGGGGGGCCTGGTGAGGGTGTGGGTTTGATTCAGAGTG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:37942562..37942801 26863196 MeRIP-seq:(Medium) rs1228672566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8196430,Human_RBP_ID_9425297 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 84147 RMVar_ID_84147 Human_SNP_ID_665140822 m1A Human chr19 - 38037296 38037296 38037296 AAGGTCTACTTATCCTTCAGGCCTCCTCCCAAACGTCAGTCCTTATGACAGACGTTCCCTGACCT AAGGTCTACTTATCCTTCAGGCCTCCTCCCAAGCGTCAGTCCTTATGACAGACGTTCCCTGACCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38037294..38037565 26863196 MeRIP-seq:(Medium) rs1039493971 Functional Loss SNV dbSNP153 33..33 33 - - - 84148 RMVar_ID_84148 Human_SNP_ID_665142537 m1A Human chr19 + 38044362 38044362 38044362 AAAAGTAGGGGTCCCCAGCACAGAGGTGTTGAAATCACGAGGAGAGCCGTGTGGATGGGGAAGAG AAAAGTAGGGGTCCCCAGCACAGAGGTGTTGATATCACGAGGAGAGCCGTGTGGATGGGGAAGAG A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38044112..38044574 26863196 MeRIP-seq:(Medium) rs1223505606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27690,RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 84149 RMVar_ID_84149 Human_SNP_ID_665142574 m1A Human chr19 + 38044491 38044491 38044491 AGGGAGGAGACCTGGAGAGTATGGACCCCTGCAGTGAGGCAGGAGGTTGATGAGGGCCCGAGGTG AGGGAGGAGACCTGGAGAGTATGGACCCCTGCGGTGAGGCAGGAGGTTGATGAGGGCCCGAGGTG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38044224..38044536 26863196 MeRIP-seq:(Medium) rs938166909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27690,RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 84150 RMVar_ID_84150 Human_SNP_ID_665146676 m1A Human chr19 - 38061605 38061605 38061605 TCTCTCCACGGCCCTGTCCTTGTCTGTCTCTCATTCTGTTTTTCTCTATATCTCTTGCACACGTG TCTCTCCACGGCCCTGTCCTTGTCTGTCTCTCTTTCTGTTTTTCTCTATATCTCTTGCACACGTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38061593..38061750 26863196 MeRIP-seq:(Medium) rs987637315 Functional Loss SNV dbSNP153 33..33 33 - - - 84151 RMVar_ID_84151 Human_SNP_ID_665173659 m1A Human chr19 - 38162335 38162335 38162335 GAATGCCTGTTGGGGGAATCTTTGCCTGCTGCATCCTGCCTGGACGGGTGCTTGTTCCCGCTGCT GAATGCCTGTTGGGGGAATCTTTGCCTGCTGCTTCCTGCCTGGACGGGTGCTTGTTCCCGCTGCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38152948..38162334 32194978 MeRIP-seq:(Medium) rs971723936 Functional Loss SNV dbSNP153 33..33 33 - - - 84152 RMVar_ID_84152 Human_SNP_ID_665182937 m1A Human chr19 + 38196504 38196486 38196505 GGGCAGAGTGTGGATGTCAAGGCGGAGCAAGGAGGTCAAGGGAGGAGCATGGAGGTCAAGGGCAG GGGCAGAGTGTGGAT___________________GTCAAGGGAGGAGCATGGAGGTCAAGGGCAG TGTCAAGGCGGAGCAAGGAG T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:38196276..38196856;chr19:38196306..38196837 26863196 MeRIP-seq:(Medium) rs550301874 Functional Loss DEL dbSNP153 16..34 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_105140,RMVar_hsa_circ_39807,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_87100,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_194532,RMVar_hsa_circ_194542,RMVar_hsa_circ_122454,RMVar_hsa_circ_14232,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543,RMVar_hsa_circ_194549,RMVar_hsa_circ_104007,RMVar_hsa_circ_52344,RMVar_hsa_circ_363638,RMVar_hsa_circ_332786 84153 RMVar_ID_84153 Human_SNP_ID_665182951 m1A Human chr19 + 38196504 38196504 38196504 GGGCAGAGTGTGGATGTCAAGGCGGAGCAAGGAGGTCAAGGGAGGAGCATGGAGGTCAAGGGCAG GGGCAGAGTGTGGATGTCAAGGCGGAGCAAGGGGGTCAAGGGAGGAGCATGGAGGTCAAGGGCAG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:38196276..38196856;chr19:38196306..38196837 26863196 MeRIP-seq:(Medium) rs1212471425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_105140,RMVar_hsa_circ_39807,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_87100,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_194532,RMVar_hsa_circ_194542,RMVar_hsa_circ_122454,RMVar_hsa_circ_14232,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543,RMVar_hsa_circ_194549,RMVar_hsa_circ_104007,RMVar_hsa_circ_52344,RMVar_hsa_circ_363638,RMVar_hsa_circ_332786 84154 RMVar_ID_84154 Human_SNP_ID_665184547 m1A Human chr19 + 38201993 38201993 38201993 GGGGACCCCCGACCCCCAGGACCACCCCTACCATGAGGTGAGGTTTCCCTGGGAACACCCGGGTT GGGGACCCCCGACCCCCAGGACCACCCCTACCGTGAGGTGAGGTTTCCCTGGGAACACCCGGGTT A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38201943..38203738 32194978 MeRIP-seq:(Medium) rs371048037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2000659 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_105140,RMVar_hsa_circ_39807,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_87100,RMVar_hsa_circ_194532,RMVar_hsa_circ_122454,RMVar_hsa_circ_14232,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543,RMVar_hsa_circ_52344,RMVar_hsa_circ_363638,RMVar_hsa_circ_48291,RMVar_hsa_circ_367959 84155 RMVar_ID_84155 Human_SNP_ID_665187210 m1A Human chr19 + 38211501 38211501 38211501 ACCGTGGGCACCAGGAGGGGCGGGTGGACACCACGCCCACCGCCCTGGGCACAAGAGGGGAAGGC ACCGTGGGCACCAGGAGGGGCGGGTGGACACCTCGCCCACCGCCCTGGGCACAAGAGGGGAAGGC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38211455..38211556 32194978 MeRIP-seq:(Medium) rs960595644 Functional Loss SNV dbSNP153 33..33 33 - - - 84156 RMVar_ID_84156 Human_SNP_ID_665197070 m1A Human chr19 - 38246263 38246263 38246263 GCCTTTTCTCACTCTCACCCTAACCTCCATCCACCCTGTTCTCTCTTCCTCTTTCCTCCAAAGGT GCCTTTTCTCACTCTCACCCTAACCTCCATCCGCCCTGTTCTCTCTTCCTCTTTCCTCCAAAGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38246251..38246393 26863196 MeRIP-seq:(Medium) rs1042407504 Functional Loss SNV dbSNP153 33..33 33 - - - 84157 RMVar_ID_84157 Human_SNP_ID_665197096 m1A Human chr19 + 38246376 38246376 38246376 GGAGCCAGCTGGGTGGGGAGGCTAGTGTGGCTACAAGGCGGGGAGGGCGGCGCATGGTGGGTTAA GGAGCCAGCTGGGTGGGGAGGCTAGTGTGGCTGCAAGGCGGGGAGGGCGGCGCATGGTGGGTTAA A G SPINT2 Ensembl:ENSG00000167642 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38246277..38246392 26863196 MeRIP-seq:(Medium) rs984021007 Functional Loss SNV dbSNP153 33..33 33 - - - 84158 RMVar_ID_84158 Human_SNP_ID_665203270 m1A Human chr19 + 38268135 38268134 38268136 AGGCCCCACCGTGTGAGAGTGAGGGTTAACTCAGGGGTCGGGGCTTCTTGTGAGAAGCATCATGT AGGCCCCACCGTGTGAGAGTGAGGGTTAACTC__GGGTCGGGGCTTCTTGTGAGAAGCATCATGT CAG C SPINT2 Ensembl:ENSG00000167642 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38268131..38268196 26863196 MeRIP-seq:(Medium) rs1271522201 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6758838 84159 RMVar_ID_84159 Human_SNP_ID_665213145 m1A Human chr19 + 38304646 38304646 38304646 CTCCATCCAGCAAGGACACCACAGCTCTTCCGACTCCAGCAGCAGCTCCAGCGATTCGGACACGG CTCCATCCAGCAAGGACACCACAGCTCTTCCGCCTCCAGCAGCAGCTCCAGCGATTCGGACACGG A C AC011479.2,C19orf33 Ensembl:ENSG00000267748,Ensembl:ENSG00000167644 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38304429..38304914 32194978 MeRIP-seq:(Medium) rs755675161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55530 Human_Splice_Rec_2001070,Human_Splice_Rec_2001071,Human_Splice_Rec_2001080,Human_Splice_Rec_2001081,Human_Splice_Rec_2001248,Human_Splice_Rec_2001249,Human_Splice_Rec_2001252,Human_Splice_Rec_2001253,Human_Splice_Rec_2001258,Human_Splice_Rec_2001259,Human_Splice_Rec_2001262,Human_Splice_Rec_2001263 84160 RMVar_ID_84160 Human_SNP_ID_665213271 m1A Human chr19 + 38304912 38304906 38304912 CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAGAAGAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA CCCGGGCAAGGCCAAGAAGCCCAAAGT______GAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA TGAAGAA T C19orf33 Ensembl:ENSG00000167644 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38304809..38305025 26863196 MeRIP-seq:(Medium) rs139805446 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_55531 Human_Splice_Rec_2001072,Human_Splice_Rec_2001082,Human_Splice_Rec_2001250,Human_Splice_Rec_2001254,Human_Splice_Rec_2001260,Human_Splice_Rec_2001264 84161 RMVar_ID_84161 Human_SNP_ID_665213272 m1A Human chr19 + 38304912 38304906 38304912 CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAGAAGAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA CCCGGGCAAGGCCAAGAAGCCCAAAGTGAA___GAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA TGAAGAA TGAA C19orf33 Ensembl:ENSG00000167644 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38304809..38305025 26863196 MeRIP-seq:(Medium) rs139805446 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_55531 Human_Splice_Rec_2001072,Human_Splice_Rec_2001082,Human_Splice_Rec_2001250,Human_Splice_Rec_2001254,Human_Splice_Rec_2001260,Human_Splice_Rec_2001264 84162 RMVar_ID_84162 Human_SNP_ID_665213275 m1A Human chr19 + 38304912 38304910 38304912 CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAGAAGAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAG__GAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA GAA G C19orf33 Ensembl:ENSG00000167644 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38304809..38305025 26863196 MeRIP-seq:(Medium) rs745359062 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_55531 Human_Splice_Rec_2001072,Human_Splice_Rec_2001082,Human_Splice_Rec_2001250,Human_Splice_Rec_2001254,Human_Splice_Rec_2001260,Human_Splice_Rec_2001264 84163 RMVar_ID_84163 Human_SNP_ID_665213283 m1A Human chr19 + 38304912 38304912 38304912 CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAGAAGAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA CCCGGGCAAGGCCAAGAAGCCCAAAGTGAAGAGGAAGGAGAAGGGCAAGAAGGAGAAGGGCAAGA A G C19orf33 Ensembl:ENSG00000167644 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38304809..38305025 26863196 MeRIP-seq:(Medium) rs577046967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55531 Human_Splice_Rec_2001072,Human_Splice_Rec_2001082,Human_Splice_Rec_2001250,Human_Splice_Rec_2001254,Human_Splice_Rec_2001260,Human_Splice_Rec_2001264 84164 RMVar_ID_84164 Human_SNP_ID_665213353 m1A Human chr19 - 38304996 38304996 38304996 GGCACCACGCTGACCAGTCGCAGAAGGCAGAGAGGAAGGTTTAATGAGCCCTGTCCAGGGCCCTT GGCACCACGCTGACCAGTCGCAGAAGGCAGAGTGGAAGGTTTAATGAGCCCTGTCCAGGGCCCTT T A YIF1B Ensembl:ENSG00000167645 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38304791..38305025 26863196 MeRIP-seq:(Medium) rs1432398890 Functional Loss SNV dbSNP153 33..33 33 - - - 84165 RMVar_ID_84165 Human_SNP_ID_665213462 m1A Human chr19 - 38305306 38305306 38305306 ACCTCCCGCTGCTGCTGCTGCTGCTGGGGGCCACTGTGGCCGCCGAACTCATCTCCTGCCTGCAG ACCTCCCGCTGCTGCTGCTGCTGCTGGGGGCCGCTGTGGCCGCCGAACTCATCTCCTGCCTGCAG T C YIF1B Ensembl:ENSG00000167645 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:38305153..38305403;chr19:38305153..38306742 32194978 MeRIP-seq:(Medium) rs1387718952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521084,Human_RBP_ID_772791,Human_RBP_ID_1015629,Human_RBP_ID_5116236,Human_RBP_ID_17386806,Human_RBP_ID_17656103,Human_RBP_ID_18945381,Human_RBP_ID_22446667,Human_RBP_ID_22764069 Human_miRNA_ID_161611,Human_miRNA_ID_939868 84166 RMVar_ID_84166 Human_SNP_ID_665213473 m1A Human chr19 + 38305323 38305323 38305323 GTTCGGCGGCCACAGTGGCCCCCAGCAGCAGCAGCAGCAGCGGGAGGTTCAGCGGGCGCGCTCAC GTTCGGCGGCCACAGTGGCCCCCAGCAGCAGCGGCAGCAGCGGGAGGTTCAGCGGGCGCGCTCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38305272..38305446 26863196 MeRIP-seq:(Medium) rs1259232323 Functional Loss SNV dbSNP153 33..33 33 - - - 84167 RMVar_ID_84167 Human_SNP_ID_665214615 m1A Human chr19 + 38309047 38309047 38309047 GGGGGGCCACCGGGGTGTCCTGTTGGTACTGCACTTCCCAGTCCTGCGGGGATGGGGAGACGGGC GGGGGGCCACCGGGGTGTCCTGTTGGTACTGCGCTTCCCAGTCCTGCGGGGATGGGGAGACGGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38308976..38309127 32194978 MeRIP-seq:(Medium) rs946114298 Functional Loss SNV dbSNP153 33..33 33 - - - 84168 RMVar_ID_84168 Human_SNP_ID_665214797 m1A Human chr19 + 38309526 38309526 38309526 CATGGGGCGTGGGAGAGGCTGCAGGATAACTCAGGCCACCAGGTGCCCGCTGGGCCCCATAGCCC CATGGGGCGTGGGAGAGGCTGCAGGATAACTCTGGCCACCAGGTGCCCGCTGGGCCCCATAGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38309476..38309660 26863196 MeRIP-seq:(Medium) rs199853490 Functional Loss SNV dbSNP153 33..33 33 - - - 84169 RMVar_ID_84169 Human_SNP_ID_665214812 m1A Human chr19 + 38309572 38309572 38309572 CCGCTGGGCCCCATAGCCCCGGCTCTGGGCTGAACTTGTGTCATCGAAAAGCTGGTGGGGGTCGG CCGCTGGGCCCCATAGCCCCGGCTCTGGGCTGCACTTGTGTCATCGAAAAGCTGGTGGGGGTCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38309521..38309666 26863196 MeRIP-seq:(Medium) rs967388675 Functional Loss SNV dbSNP153 33..33 33 - - - 84170 RMVar_ID_84170 Human_SNP_ID_665215880 m1A Human chr19 + 38313769 38313769 38313769 CAGGCCCCGACTCTGCCAAGCTCCTTGCCCCCACTGGCTTTTGAATATGCAGAGCTTTCATCCTG CAGGCCCCGACTCTGCCAAGCTCCTTGCCCCCCCTGGCTTTTGAATATGCAGAGCTTTCATCCTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38313763..38313850 26863196 MeRIP-seq:(Medium) rs936838468 Functional Loss SNV dbSNP153 33..33 33 - - - 84171 RMVar_ID_84171 Human_SNP_ID_665215881 m1A Human chr19 + 38313769 38313769 38313769 CAGGCCCCGACTCTGCCAAGCTCCTTGCCCCCACTGGCTTTTGAATATGCAGAGCTTTCATCCTG CAGGCCCCGACTCTGCCAAGCTCCTTGCCCCCGCTGGCTTTTGAATATGCAGAGCTTTCATCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38313763..38313850 26863196 MeRIP-seq:(Medium) rs936838468 Functional Loss SNV dbSNP153 33..33 33 - - - 84172 RMVar_ID_84172 Human_SNP_ID_665222194 m1A Human chr19 + 38336974 38336950 38336974 GGGGCAGGGCCAGGAGCAAGAGCAGGGGCGGGACCAGGAGCAAGTGCAGAGGCGGAGCCAGGAAC GGGGCAGGG________________________CCAGGAGCAAGTGCAGAGGCGGAGCCAGGAAC GCCAGGAGCAAGAGCAGGGGCGGGA G CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38336851..38336995 26863196 MeRIP-seq:(Medium) rs1214921418 Functional Loss DEL dbSNP153 10..33 33 - - - 84173 RMVar_ID_84173 Human_SNP_ID_665223335 m1A Human chr19 - 38341104 38341104 38341104 CCTGACCTCTCCTCCCACACTCCCTCTCACTCACTCTGCTCCAGCCACAAAGTCCTCTTCATAGT CCTGACCTCTCCTCCCACACTCCCTCTCACTCGCTCTGCTCCAGCCACAAAGTCCTCTTCATAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38341054..38341159 26863196 MeRIP-seq:(Medium) rs1457642205 Functional Loss SNV dbSNP153 33..33 33 - - - 84174 RMVar_ID_84174 Human_SNP_ID_665223336 m1A Human chr19 - 38341104 38341104 38341104 CCTGACCTCTCCTCCCACACTCCCTCTCACTCACTCTGCTCCAGCCACAAAGTCCTCTTCATAGT CCTGACCTCTCCTCCCACACTCCCTCTCACTCCCTCTGCTCCAGCCACAAAGTCCTCTTCATAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38341054..38341159 26863196 MeRIP-seq:(Medium) rs1457642205 Functional Loss SNV dbSNP153 33..33 33 - - - 84175 RMVar_ID_84175 Human_SNP_ID_665233427 m1A Human chr19 + 38374848 38374848 38374848 CGGCAGGCTTCTCGAGCTCCGGGCCCGCGGCAACCTCGGGCGCTGTTCTGCAGGCCGCGACCGGC CGGCAGGCTTCTCGAGCTCCGGGCCCGCGGCATCCTCGGGCGCTGTTCTGCAGGCCGCGACCGGC A T PSMD8 Ensembl:ENSG00000099341 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38374797..38374880 26863196 MeRIP-seq:(Medium) rs772319675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139505,Human_RBP_ID_241172,Human_RBP_ID_773446,Human_RBP_ID_1563846,Human_RBP_ID_4525730,Human_RBP_ID_5320336,Human_RBP_ID_8486343,Human_RBP_ID_8833506,Human_RBP_ID_9330006,Human_RBP_ID_17923954,Human_RBP_ID_22446677 84176 RMVar_ID_84176 Human_SNP_ID_665233446 m1A Human chr19 + 38374875 38374875 38374875 CGGCAACCTCGGGCGCTGTTCTGCAGGCCGCGACCGGCATGTACGAGCAACTCAAGGGCGAGTGG CGGCAACCTCGGGCGCTGTTCTGCAGGCCGCGGCCGGCATGTACGAGCAACTCAAGGGCGAGTGG A G PSMD8 Ensembl:ENSG00000099341 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:38374732..38375026 26863410 MeRIP-seq:(Medium) rs1259073199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139505,Human_RBP_ID_1015639,Human_RBP_ID_1563847,Human_RBP_ID_4525730,Human_RBP_ID_5320336,Human_RBP_ID_8486343,Human_RBP_ID_9330006,Human_RBP_ID_17268847,Human_RBP_ID_18731503,Human_RBP_ID_22446677,Human_RBP_ID_23796301 Human_Splice_Rec_2001621,Human_Splice_Rec_2001633,Human_Splice_Rec_2001645,Human_Splice_Rec_2001649,Human_Splice_Rec_2001661,Human_Splice_Rec_2001665,Human_Splice_Rec_2001675 84177 RMVar_ID_84177 Human_SNP_ID_665233452 m1A Human chr19 - 38374882 38374882 38374882 TACGGTTCCACTCGCCCTTGAGTTGCTCGTACATGCCGGTCGCGGCCTGCAGAACAGCGCCCGAG TACGGTTCCACTCGCCCTTGAGTTGCTCGTACCTGCCGGTCGCGGCCTGCAGAACAGCGCCCGAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38374831..38375026 32194978 MeRIP-seq:(Medium) rs759581453 Functional Loss SNV dbSNP153 33..33 33 - - - 84178 RMVar_ID_84178 Human_SNP_ID_665233594 m1A Human chr19 + 38375345 38375345 38375345 ACCCACGCGGGGGTGGTGGGGGAATGATTGGAAGACTTATGGCAGAACTGAGTGAGGGGTTAGAT ACCCACGCGGGGGTGGTGGGGGAATGATTGGAGGACTTATGGCAGAACTGAGTGAGGGGTTAGAT A G PSMD8 Ensembl:ENSG00000099341 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38375343..38375594 26863196 MeRIP-seq:(Medium) rs984841688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194558,RMVar_hsa_circ_105002 84179 RMVar_ID_84179 Human_SNP_ID_665235489 m1A Human chr19 - 38382106 38382106 38382106 GATGCACCCAGCGATCTCATCCCTGGGGGAAGATGAGAAGCTCCTCATTACTGAGCATCAACAAC GATGCACCCAGCGATCTCATCCCTGGGGGAAGGTGAGAAGCTCCTCATTACTGAGCATCAACAAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38382101..38382250 32194978 MeRIP-seq:(Medium) rs1451698952 Functional Loss SNV dbSNP153 33..33 33 - - - 84180 RMVar_ID_84180 Human_SNP_ID_665235927 m1A Human chr19 - 38383427 38383427 38383427 TTGGGCGAAACCCTGCAGTGTAACTGTTTTAAATAACTCGTGCCCTGCCCCACCCAGTGCCCGGG TTGGGCGAAACCCTGCAGTGTAACTGTTTTAAGTAACTCGTGCCCTGCCCCACCCAGTGCCCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38383376..38383475 32194978 MeRIP-seq:(Medium) rs758497238 Functional Loss SNV dbSNP153 33..33 33 - - - 84181 RMVar_ID_84181 Human_SNP_ID_665236442 m1A Human chr19 - 38385369 38385367 38385369 AGGAGGGTGCCGAACCCCAGACTGCTGGATAGAGTCCTACTCAGCCCTTTGGCTTCCTGACCCTA AGGAGGGTGCCGAACCCCAGACTGCTGGATAG__TCCTACTCAGCCCTTTGGCTTCCTGACCCTA ACT A GGN Ensembl:ENSG00000179168 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38385318..38385423 26863196 MeRIP-seq:(Medium) rs1386271529 Functional Loss DEL dbSNP153 33..34 33 - - - 84182 RMVar_ID_84182 Human_SNP_ID_665237357 m1A Human chr19 + 38386951 38386951 38386951 CGGGCTTTTGCCATTTAGACGGGCCGGGCAGCAGAGTCCCCGCGGGGGCCGGGGGTGGTGCAGAG CGGGCTTTTGCCATTTAGACGGGCCGGGCAGCGGAGTCCCCGCGGGGGCCGGGGGTGGTGCAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38386901..38387111 26863196 MeRIP-seq:(Medium) rs1342120401 Functional Loss SNV dbSNP153 33..33 33 - - - 84183 RMVar_ID_84183 Human_SNP_ID_665238335 m1A Human chr19 + 38390074 38390071 38390074 GGTGGGTACAGAGAGAAAGGGCAGACATGGAGAAGAAGATAGAGGTGAGAGAGAAGAGATGGCAT GGTGGGTACAGAGAGAAAGGGCAGACATGG___AGAAGATAGAGGTGAGAGAGAAGAGATGGCAT GAGA G SPRED3 Ensembl:ENSG00000188766 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38390024..38390611 26863196 MeRIP-seq:(Medium) rs1168072058 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_263918,Human_RBP_ID_9427252,Human_RBP_ID_22665353 Human_Splice_Rec_2001745 84184 RMVar_ID_84184 Human_SNP_ID_665241913 m1A Human chr19 + 38403200 38403200 38403200 GGCGGAAGCGTGGGAGGGGGCCGCGGTGGCCCAGGACCTGCTGGCTCTGGGGTAAAAGGGTGTGC GGCGGAAGCGTGGGAGGGGGCCGCGGTGGCCCGGGACCTGCTGGCTCTGGGGTAAAAGGGTGTGC A G FAM98C Ensembl:ENSG00000130244 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:38403126..38403546;chr19:38403126..38403585 26863196 MeRIP-seq:(Medium) rs776960731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2001777,Human_Splice_Rec_2001785,Human_Splice_Rec_2001799,Human_Splice_Rec_2001809,Human_Splice_Rec_2001825 84185 RMVar_ID_84185 Human_SNP_ID_665242681 m1A Human chr19 - 38405611 38405611 38405611 CACCACACCTCTGCCCGGTCACTCCAGTGGAAAGCAGATGTAGTGAGGTCAAGGCGCTTGAGGAG CACCACACCTCTGCCCGGTCACTCCAGTGGAACGCAGATGTAGTGAGGTCAAGGCGCTTGAGGAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38405342..38405647 26863196 MeRIP-seq:(Medium) rs928999588 Functional Loss SNV dbSNP153 33..33 33 - - - 84186 RMVar_ID_84186 Human_SNP_ID_665243658 m1A Human chr19 - 38408880 38408875 38408880 GACCCCCCGCCCCCGACCACCAGTCCCCCTTTACTTCTTCTTCTTCTTCTTGCGACCCCAACACT GACCCCCCGCCCCCGACCACCAGTCCCCCTTT_____TTCTTCTTCTTCTTGCGACCCCAACACT AGAAGT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38408837..38408988 32194978 MeRIP-seq:(Medium) rs1233548941 Functional Loss DEL dbSNP153 33..37 33 - - - 84187 RMVar_ID_84187 Human_SNP_ID_665243662 m1A Human chr19 - 38408880 38408880 38408880 GACCCCCCGCCCCCGACCACCAGTCCCCCTTTACTTCTTCTTCTTCTTCTTGCGACCCCAACACT GACCCCCCGCCCCCGACCACCAGTCCCCCTTTCCTTCTTCTTCTTCTTCTTGCGACCCCAACACT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38408837..38408988 32194978 MeRIP-seq:(Medium) rs1481125245 Functional Loss SNV dbSNP153 33..33 33 - - - 84188 RMVar_ID_84188 Human_SNP_ID_665243707 m1A Human chr19 + 38408985 38408985 38408985 CCGTTTAAGGCTTTCCTTGGTATTTGGCACCCAAGCCCCCCATCTCCTATTCCTGAGTCCCCAAA CCGTTTAAGGCTTTCCTTGGTATTTGGCACCCTAGCCCCCCATCTCCTATTCCTGAGTCCCCAAA A T FAM98C Ensembl:ENSG00000130244 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38408940..38409013 26863196 MeRIP-seq:(Medium) rs1231783785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521132,Human_RBP_ID_1015659,Human_RBP_ID_5116875,Human_RBP_ID_5145745,Human_RBP_ID_17657022,Human_RBP_ID_17924000,Human_RBP_ID_18946800,Human_RBP_ID_26472455,Human_RBP_ID_26817464 RMVar_hsa_circ_114987,RMVar_hsa_circ_194566 84189 RMVar_ID_84189 Human_SNP_ID_665289417 m1A Human chr19 + 38565509 38565509 38565509 AGGCATGCCCGACCCCACCAGCGACGAGGTGCACGGCGAGCAGCCGGCCGGGCCGGGCGGAGACG AGGCATGCCCGACCCCACCAGCGACGAGGTGCGCGGCGAGCAGCCGGCCGGGCCGGGCGGAGACG A G RYR1 Ensembl:ENSG00000196218 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38565499..38565656 26863196 MeRIP-seq:(Medium) rs1408526429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75754,RMVar_hsa_circ_194567,RMVar_hsa_circ_98080,RMVar_hsa_circ_194575,RMVar_hsa_circ_78119,RMVar_hsa_circ_194576,RMVar_hsa_circ_82620,RMVar_hsa_circ_194579,RMVar_hsa_circ_80741,RMVar_hsa_circ_86726,RMVar_hsa_circ_266169,RMVar_hsa_circ_194581,RMVar_hsa_circ_93276,RMVar_hsa_circ_194582,RMVar_hsa_circ_194583 84190 RMVar_ID_84190 Human_SNP_ID_665289489 m1A Human chr19 + 38565602 38565602 38565602 TGGAGACGCCGCGGAGGGCGCTGGAGACGAGGAGGAGGCGGTGCACGAGGCCGGGCCGGGCGGTG TGGAGACGCCGCGGAGGGCGCTGGAGACGAGGCGGAGGCGGTGCACGAGGCCGGGCCGGGCGGTG A C RYR1 Ensembl:ENSG00000196218 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38565199..38567773 26863196 MeRIP-seq:(Medium) rs1358394495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75754,RMVar_hsa_circ_194567,RMVar_hsa_circ_98080,RMVar_hsa_circ_194575,RMVar_hsa_circ_78119,RMVar_hsa_circ_194576,RMVar_hsa_circ_82620,RMVar_hsa_circ_194579,RMVar_hsa_circ_80741,RMVar_hsa_circ_86726,RMVar_hsa_circ_266169,RMVar_hsa_circ_194581,RMVar_hsa_circ_93276,RMVar_hsa_circ_194582,RMVar_hsa_circ_194583 84191 RMVar_ID_84191 Human_SNP_ID_665289490 m1A Human chr19 + 38565602 38565602 38565602 TGGAGACGCCGCGGAGGGCGCTGGAGACGAGGAGGAGGCGGTGCACGAGGCCGGGCCGGGCGGTG TGGAGACGCCGCGGAGGGCGCTGGAGACGAGGGGGAGGCGGTGCACGAGGCCGGGCCGGGCGGTG A G RYR1 Ensembl:ENSG00000196218 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38565199..38567773 26863196 MeRIP-seq:(Medium) rs1358394495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75754,RMVar_hsa_circ_194567,RMVar_hsa_circ_98080,RMVar_hsa_circ_194575,RMVar_hsa_circ_78119,RMVar_hsa_circ_194576,RMVar_hsa_circ_82620,RMVar_hsa_circ_194579,RMVar_hsa_circ_80741,RMVar_hsa_circ_86726,RMVar_hsa_circ_266169,RMVar_hsa_circ_194581,RMVar_hsa_circ_93276,RMVar_hsa_circ_194582,RMVar_hsa_circ_194583 84192 RMVar_ID_84192 Human_SNP_ID_665308894 m1A Human chr19 + 38629714 38629714 38629714 ACCACAGACCTAACCTTTGAGCAGAAATCTGAAGGAGGTGAGGGTGGTAGCCATGGAGGAGAATT ACCACAGACCTAACCTTTGAGCAGAAATCTGAGGGAGGTGAGGGTGGTAGCCATGGAGGAGAATT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38629710..38629911 26863196 MeRIP-seq:(Medium) rs1290562876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6759280,Human_RBP_ID_13448804 RMVar_hsa_circ_9628,RMVar_hsa_circ_115504,RMVar_hsa_circ_87615,RMVar_hsa_circ_194620,RMVar_hsa_circ_83285,RMVar_hsa_circ_81561,RMVar_hsa_circ_194621,RMVar_hsa_circ_194622,RMVar_hsa_circ_331256,RMVar_hsa_circ_111904,RMVar_hsa_circ_15078,RMVar_hsa_circ_194628,RMVar_hsa_circ_194629,RMVar_hsa_circ_194627,RMVar_hsa_circ_85236,RMVar_hsa_circ_194630 84193 RMVar_ID_84193 Human_SNP_ID_665309750 m1A Human chr19 + 38632480 38632480 38632480 ATGGACCTCTTGGAAGGTATAACTGGCTTTGAAGACTCTGTCCGAAAGTGTAAGTCCCTCTCTGA ATGGACCTCTTGGAAGGTATAACTGGCTTTGAGGACTCTGTCCGAAAGTGTAAGTCCCTCTCTGA A G EIF3K Ensembl:ENSG00000178982 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38632419..38632520 32194978 MeRIP-seq:(Medium) rs369298575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521152,Human_RBP_ID_1015670,Human_RBP_ID_1563993,Human_RBP_ID_1886976,Human_RBP_ID_4525856,Human_RBP_ID_6759308,Human_RBP_ID_8486455,Human_RBP_ID_9380961,Human_RBP_ID_19093268,Human_RBP_ID_23796361 Human_Splice_Rec_2003314,Human_Splice_Rec_2003315,Human_Splice_Rec_2003328,Human_Splice_Rec_2003329,Human_Splice_Rec_2003354,Human_Splice_Rec_2003355,Human_Splice_Rec_2003374,Human_Splice_Rec_2003375,Human_Splice_Rec_2003388,Human_Splice_Rec_2003389,Human_Splice_Rec_2003412,Human_Splice_Rec_2003413,Human_Splice_Rec_2003424,Human_Splice_Rec_2003425,Human_Splice_Rec_2003430,Human_Splice_Rec_2003431 RMVar_hsa_circ_9628,RMVar_hsa_circ_115504,RMVar_hsa_circ_87615,RMVar_hsa_circ_194620,RMVar_hsa_circ_83285,RMVar_hsa_circ_31485,RMVar_hsa_circ_81561,RMVar_hsa_circ_194621,RMVar_hsa_circ_194622,RMVar_hsa_circ_331256,RMVar_hsa_circ_111904,RMVar_hsa_circ_15078,RMVar_hsa_circ_194628,RMVar_hsa_circ_194629,RMVar_hsa_circ_194627,RMVar_hsa_circ_85236,RMVar_hsa_circ_278329,RMVar_hsa_circ_194630,RMVar_hsa_circ_90957,RMVar_hsa_circ_194631,RMVar_hsa_circ_194632 84194 RMVar_ID_84194 Human_SNP_ID_665310558 m1A Human chr19 + 38635031 38635031 38635031 AGCTAAAGGTGTGGATGAGCAAATACGGCTGGAGTGCCGACGAGTCGGGGCAGATCTTCATCTGT AGCTAAAGGTGTGGATGAGCAAATACGGCTGGGGTGCCGACGAGTCGGGGCAGATCTTCATCTGT A G EIF3K Ensembl:ENSG00000178982 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38634976..38635075 26863196 MeRIP-seq:(Medium) rs77863139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521154,Human_RBP_ID_909578,Human_RBP_ID_4525862,Human_RBP_ID_9330009,Human_RBP_ID_9382474,Human_RBP_ID_13448908,Human_RBP_ID_17655608,Human_RBP_ID_17695561,Human_RBP_ID_17924020,Human_RBP_ID_22446686,Human_RBP_ID_23210942 Human_Splice_Rec_2003318,Human_Splice_Rec_2003319,Human_Splice_Rec_2003332,Human_Splice_Rec_2003333,Human_Splice_Rec_2003358,Human_Splice_Rec_2003378,Human_Splice_Rec_2003379,Human_Splice_Rec_2003392,Human_Splice_Rec_2003416,Human_Splice_Rec_2003426,Human_Splice_Rec_2003427,Human_Splice_Rec_2003434,Human_Splice_Rec_2003435 Human_miRNA_ID_2152290,Human_miRNA_ID_2975025,Human_miRNA_ID_3008222 RMVar_hsa_circ_115504,RMVar_hsa_circ_87615,RMVar_hsa_circ_194620,RMVar_hsa_circ_31485,RMVar_hsa_circ_81561,RMVar_hsa_circ_194621,RMVar_hsa_circ_15078,RMVar_hsa_circ_194629,RMVar_hsa_circ_85236,RMVar_hsa_circ_194630,RMVar_hsa_circ_90957,RMVar_hsa_circ_124726,RMVar_hsa_circ_194632,RMVar_hsa_circ_92925,RMVar_hsa_circ_194633,RMVar_hsa_circ_194635 84195 RMVar_ID_84195 Human_SNP_ID_665314271 m1A Human chr19 + 38647734 38647734 38647734 GAGGCGGGAGCGGACAGGCTGGTGGGCGAGCGAGAGGCGGCGGAATGGTGGACTACCACGCGGCG GAGGCGGGAGCGGACAGGCTGGTGGGCGAGCGGGAGGCGGCGGAATGGTGGACTACCACGCGGCG A G ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38647576..38649444 26863196 MeRIP-seq:(Medium) rs765202375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53949,Human_RBP_ID_771613,Human_RBP_ID_826016,Human_RBP_ID_914336,Human_RBP_ID_1067516,Human_RBP_ID_3954959,Human_RBP_ID_4525879,Human_RBP_ID_5320338,Human_RBP_ID_6759369,Human_RBP_ID_8839986,Human_RBP_ID_8942213,Human_RBP_ID_9259002,Human_RBP_ID_9293633,Human_RBP_ID_9328917,Human_RBP_ID_9380962,Human_RBP_ID_9426145,Human_RBP_ID_18193040,Human_RBP_ID_18420924,Human_RBP_ID_22070169,Human_RBP_ID_22446687,Human_RBP_ID_22533395,Human_RBP_ID_22971702,Human_RBP_ID_26336217,Human_RBP_ID_26989339,Human_RBP_ID_27573108 RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637 84196 RMVar_ID_84196 Human_SNP_ID_665314277 m1A Human chr19 - 38647750 38647750 38647750 ACTGGTACGACTGGTTCGCCGCGTGGTAGTCCACCATTCCGCCGCCTCTCGCTCGCCCACCAGCC ACTGGTACGACTGGTTCGCCGCGTGGTAGTCCTCCATTCCGCCGCCTCTCGCTCGCCCACCAGCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type chr19:38647676..38647968;chr19:38647650..38647850 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 84197 RMVar_ID_84197 Human_SNP_ID_665314278 m1A Human chr19 - 38647750 38647750 38647750 ACTGGTACGACTGGTTCGCCGCGTGGTAGTCCACCATTCCGCCGCCTCTCGCTCGCCCACCAGCC ACTGGTACGACTGGTTCGCCGCGTGGTAGTCCCCCATTCCGCCGCCTCTCGCTCGCCCACCAGCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type chr19:38647676..38647968;chr19:38647650..38647850 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 84198 RMVar_ID_84198 Human_SNP_ID_665317585 m1A Human chr19 + 38660926 38660926 38660926 GAGGGGAGGAGTGTGCAGTGCAGGTACTTCAGATGGAGAGGAAGGTCTCAAAGAGGTGGCATTTC GAGGGGAGGAGTGTGCAGTGCAGGTACTTCAGCTGGAGAGGAAGGTCTCAAAGAGGTGGCATTTC A C ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38660924..38661031 26863196 MeRIP-seq:(Medium) rs988865395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9425306,Human_RBP_ID_13449371,Human_RBP_ID_17190828 RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637 84199 RMVar_ID_84199 Human_SNP_ID_665318216 m1A Human chr19 + 38663401 38663401 38663401 GAGAGAAACCGGAGACCTGGTCCGTGCTCTCAAAGAGCTCGCGGTGTAGCTGGGGAGAGAGCAAG GAGAGAAACCGGAGACCTGGTCCGTGCTCTCACAGAGCTCGCGGTGTAGCTGGGGAGAGAGCAAG A C ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38663399..38663615 26863196 MeRIP-seq:(Medium) rs536355699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6759558 RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637 84200 RMVar_ID_84200 Human_SNP_ID_665321482 m1A Human chr19 - 38674194 38674194 38674194 TGAGGTTGGCTCTAACTCTCCCTCCAGGCCTCACTTCACTGTCATCATCTTGGAAAGTCTCCCCT TGAGGTTGGCTCTAACTCTCCCTCCAGGCCTCGCTTCACTGTCATCATCTTGGAAAGTCTCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38674192..38674347 26863196 MeRIP-seq:(Medium) rs560194373 Functional Loss SNV dbSNP153 33..33 33 - - - 84201 RMVar_ID_84201 Human_SNP_ID_665328325 m1A Human chr19 + 38700638 38700638 38700638 ACGGCATGGTGCAACTCCCACCTGCGGAAGGCAGGCACACAGATCGAGAACATTGATGAGGACTT ACGGCATGGTGCAACTCCCACCTGCGGAAGGCGGGCACACAGATCGAGAACATTGATGAGGACTT A G ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38700601..38700650 26863196 MeRIP-seq:(Medium) rs772894941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53961,Human_RBP_ID_521163,Human_RBP_ID_1015675,Human_RBP_ID_1564031,Human_RBP_ID_1887024,Human_RBP_ID_8839317,Human_RBP_ID_9293636,Human_RBP_ID_22449408 Human_Splice_Rec_2003438,Human_Splice_Rec_2003439,Human_Splice_Rec_2003460,Human_Splice_Rec_2003461,Human_Splice_Rec_2003526,Human_Splice_Rec_2003527,Human_Splice_Rec_2003530,Human_Splice_Rec_2003548,Human_Splice_Rec_2003549 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_301913,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_194639 84202 RMVar_ID_84202 Human_SNP_ID_665328326 m1A Human chr19 + 38700644 38700644 38700644 TGGTGCAACTCCCACCTGCGGAAGGCAGGCACACAGATCGAGAACATTGATGAGGACTTCCGAGA TGGTGCAACTCCCACCTGCGGAAGGCAGGCACGCAGATCGAGAACATTGATGAGGACTTCCGAGA A G ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38647726..38701060 32194978 MeRIP-seq:(Medium) rs111387742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53961,Human_RBP_ID_521163,Human_RBP_ID_1564031,Human_RBP_ID_1887024,Human_RBP_ID_3571298,Human_RBP_ID_5190647,Human_RBP_ID_5585656,Human_RBP_ID_8486533,Human_RBP_ID_13450029,Human_RBP_ID_18532436,Human_RBP_ID_18731665,Human_RBP_ID_20349360,Human_RBP_ID_22449408,Human_RBP_ID_22810651,Human_RBP_ID_27273757,Human_RBP_ID_27467706 Human_Splice_Rec_2003438,Human_Splice_Rec_2003439,Human_Splice_Rec_2003460,Human_Splice_Rec_2003461,Human_Splice_Rec_2003526,Human_Splice_Rec_2003527,Human_Splice_Rec_2003530,Human_Splice_Rec_2003548,Human_Splice_Rec_2003549 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_301913,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_194639 84203 RMVar_ID_84203 Human_SNP_ID_665328482 m1A Human chr19 + 38701109 38701109 38701109 TTATTGCCAGCAAAGGCGTCAAGCTGGTCTCCATCGGGGCAGAAGGTGAGCTGGAGGTGGGGCAG TTATTGCCAGCAAAGGCGTCAAGCTGGTCTCCGTCGGGGCAGAAGGTGAGCTGGAGGTGGGGCAG A G ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38700966..38701115 26863196 MeRIP-seq:(Medium) rs761068296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769491,Human_RBP_ID_1015677,Human_RBP_ID_8833524,Human_RBP_ID_9292099,Human_RBP_ID_9380963,Human_RBP_ID_17924050,Human_RBP_ID_26334906,Human_RBP_ID_26815789,Human_RBP_ID_27815408 Human_Splice_Rec_2003441,Human_Splice_Rec_2003463,Human_Splice_Rec_2003551 Human_miRNA_ID_2152292,Human_miRNA_ID_2420756 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_301913,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_94201,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_194639,RMVar_hsa_circ_194642 84204 RMVar_ID_84204 Human_SNP_ID_665329315 m1A Human chr19 + 38704372 38704372 38704372 TGGATTATGGGCGGGAAGGGTACATAGGAGGCAGCCGCATTGAGCTCTGGAGATGACAGTGGCTT TGGATTATGGGCGGGAAGGGTACATAGGAGGCGGCCGCATTGAGCTCTGGAGATGACAGTGGCTT A G ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38704367..38704460 26863196 MeRIP-seq:(Medium) rs1218148211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6759759,Human_RBP_ID_9346961,Human_RBP_ID_13450096 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_94201,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_194642 84205 RMVar_ID_84205 Human_SNP_ID_665329516 m1A Human chr19 + 38705061 38705060 38705061 CACCTGTACTGCCCCCGCTTCCCACCTGAGTCAGGGCGGGTTAGAGGAGAGCTGAAGTGTGATCT CACCTGTACTGCCCCCGCTTCCCACCTGAGTC_GGGCGGGTTAGAGGAGAGCTGAAGTGTGATCT CA C ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38705059..38705163 32194978 MeRIP-seq:(Medium) rs1287727198 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_19090056,Human_RBP_ID_22359001 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_88533,RMVar_hsa_circ_94201,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_269306,RMVar_hsa_circ_194642,RMVar_hsa_circ_194644,RMVar_hsa_circ_35918,RMVar_hsa_circ_194645 84206 RMVar_ID_84206 Human_SNP_ID_665329517 m1A Human chr19 + 38705061 38705061 38705061 CACCTGTACTGCCCCCGCTTCCCACCTGAGTCAGGGCGGGTTAGAGGAGAGCTGAAGTGTGATCT CACCTGTACTGCCCCCGCTTCCCACCTGAGTCCGGGCGGGTTAGAGGAGAGCTGAAGTGTGATCT A C ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38705059..38705163 32194978 MeRIP-seq:(Medium) rs771501637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090056,Human_RBP_ID_22359001 RMVar_hsa_circ_24110,RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_357674,RMVar_hsa_circ_274277,RMVar_hsa_circ_88533,RMVar_hsa_circ_94201,RMVar_hsa_circ_194640,RMVar_hsa_circ_194641,RMVar_hsa_circ_269306,RMVar_hsa_circ_194642,RMVar_hsa_circ_194644,RMVar_hsa_circ_35918,RMVar_hsa_circ_194645 84207 RMVar_ID_84207 Human_SNP_ID_665330769 m1A Human chr19 + 38710210 38710210 38710210 GGAGCCCGTGGATCCCAGTGAGTGACGCCTCCACCCCCCGCCCTACTCGGGCAGTTTAACCCTTG GGAGCCCGTGGATCCCAGTGAGTGACGCCTCCCCCCCCCGCCCTACTCGGGCAGTTTAACCCTTG A C ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38710208..38710288 26863196 MeRIP-seq:(Medium) rs747236797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_373386,RMVar_hsa_circ_194637,RMVar_hsa_circ_24682,RMVar_hsa_circ_88533,RMVar_hsa_circ_94201,RMVar_hsa_circ_194641,RMVar_hsa_circ_194642,RMVar_hsa_circ_74933,RMVar_hsa_circ_194645,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_61196,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_83803,RMVar_hsa_circ_194650,RMVar_hsa_circ_194651 84208 RMVar_ID_84208 Human_SNP_ID_665330948 m1A Human chr19 - 38710731 38710731 38710731 CATCTAGCAGCTCCTGCTGCAAGTACCTGCTCACTTCACCCCTCCACATTGACAGCACCAGCTGA CATCTAGCAGCTCCTGCTGCAAGTACCTGCTCTCTTCACCCCTCCACATTGACAGCACCAGCTGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38710723..38710849 26863196 MeRIP-seq:(Medium) rs1387168336 Functional Loss SNV dbSNP153 33..33 33 - - - 84209 RMVar_ID_84209 Human_SNP_ID_665332650 m1A Human chr19 + 38717275 38717275 38717275 TCAACACGCTGCAGACCAAGCTGCGCCTCAGCAACCGGCCCGCCTTCATGCCCTCCGAGGGCAAG TCAACACGCTGCAGACCAAGCTGCGCCTCAGCTACCGGCCCGCCTTCATGCCCTCCGAGGGCAAG A T ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:38717158..38717350;chr19:38717154..38717325 26863196 MeRIP-seq:(Medium) rs1252156542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8833540,Human_RBP_ID_9294417,Human_RBP_ID_9382481,Human_RBP_ID_22447717 Human_Splice_Rec_2003455,Human_Splice_Rec_2003477,Human_Splice_Rec_2003503 RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637,RMVar_hsa_circ_5546,RMVar_hsa_circ_94201,RMVar_hsa_circ_194642,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_83803,RMVar_hsa_circ_45985,RMVar_hsa_circ_194650,RMVar_hsa_circ_194651,RMVar_hsa_circ_63039,RMVar_hsa_circ_23347,RMVar_hsa_circ_125866,RMVar_hsa_circ_324742,RMVar_hsa_circ_67041,RMVar_hsa_circ_194653,RMVar_hsa_circ_194654 84210 RMVar_ID_84210 Human_SNP_ID_665333854 m1A Human chr19 + 38721589 38721589 38721589 GCACCGGGACTACGAGACGGCCACACTATCGGACATCAAAGCCCTCATTCGCAAGCACGAGGCCT GCACCGGGACTACGAGACGGCCACACTATCGGCCATCAAAGCCCTCATTCGCAAGCACGAGGCCT A C ACTN4 Ensembl:ENSG00000130402 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38721501..38721724 26863196 MeRIP-seq:(Medium) rs775858826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53981,Human_RBP_ID_1564121,Human_RBP_ID_1887057,Human_RBP_ID_8486581,Human_RBP_ID_8833545,Human_RBP_ID_17268869,Human_RBP_ID_18532440,Human_RBP_ID_27467712 Human_Splice_Rec_2003458,Human_Splice_Rec_2003480,Human_Splice_Rec_2003481,Human_Splice_Rec_2003506,Human_Splice_Rec_2003507 RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637,RMVar_hsa_circ_94201,RMVar_hsa_circ_194642,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_83803,RMVar_hsa_circ_194650,RMVar_hsa_circ_194651,RMVar_hsa_circ_63039,RMVar_hsa_circ_105793,RMVar_hsa_circ_23347,RMVar_hsa_circ_125866,RMVar_hsa_circ_194654,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_194655,RMVar_hsa_circ_123111,RMVar_hsa_circ_194656 84211 RMVar_ID_84211 Human_SNP_ID_665334461 m1A Human chr19 + 38723700 38723700 38723700 TGACCAGTGGGACGCCCTCGGCTCTCTGACACATAGTCGCAGGGAAGCCCTGGAGGTGAGGAGGG TGACCAGTGGGACGCCCTCGGCTCTCTGACACGTAGTCGCAGGGAAGCCCTGGAGGTGAGGAGGG A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38723626..38723725 32194978 MeRIP-seq:(Medium) rs1215605858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1015686,Human_RBP_ID_6759830,Human_RBP_ID_8833549,Human_RBP_ID_9293651,Human_RBP_ID_22446700,Human_RBP_ID_22971831 Human_Splice_Rec_2003482,Human_Splice_Rec_2003483,Human_Splice_Rec_2003508,Human_Splice_Rec_2003509,Human_Splice_Rec_2003531 RMVar_hsa_circ_194638,RMVar_hsa_circ_77110,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_194651,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_124372,RMVar_hsa_circ_194657 84212 RMVar_ID_84212 Human_SNP_ID_665334656 m1A Human chr19 + 38724190 38724190 38724190 GCCTGATCTCAGCCCATGACCAGTTCAAGTCCACCCTGCCGGACGCCGATAGGGAGCGCGAGGCC GCCTGATCTCAGCCCATGACCAGTTCAAGTCCGCCCTGCCGGACGCCGATAGGGAGCGCGAGGCC A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:38723926..38724225 26863196 MeRIP-seq:(Medium) rs781208908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53985,Human_RBP_ID_1564123,Human_RBP_ID_1887060,Human_RBP_ID_3956857,Human_RBP_ID_8833553,Human_RBP_ID_9259010,Human_RBP_ID_9293654,Human_RBP_ID_9380973,Human_RBP_ID_18192227,Human_RBP_ID_18441251,Human_RBP_ID_18731732,Human_RBP_ID_22447722,Human_RBP_ID_24484270,Human_RBP_ID_26336225,Human_RBP_ID_26989399 Human_Splice_Rec_2003486,Human_Splice_Rec_2003512,Human_Splice_Rec_2003534 RMVar_hsa_circ_194638,RMVar_hsa_circ_77110,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_194651,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_89445,RMVar_hsa_circ_124372,RMVar_hsa_circ_194657,RMVar_hsa_circ_194658 84213 RMVar_ID_84213 Human_SNP_ID_665334772 m1A Human chr19 + 38724435 38724435 38724435 CGCTCCCACACCGCGTCTCCTCTGCCAGGTGCAGCAGCTGGTGCCAAAACGGGACCATGCCCTCC CGCTCCCACACCGCGTCTCCTCTGCCAGGTGCTGCAGCTGGTGCCAAAACGGGACCATGCCCTCC A T ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs780698414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914349,Human_RBP_ID_4526001,Human_RBP_ID_5373828,Human_RBP_ID_9294421,Human_RBP_ID_9380976,Human_RBP_ID_18192229,Human_RBP_ID_18470725,Human_RBP_ID_22449417,Human_RBP_ID_22663889,Human_RBP_ID_22719209,Human_RBP_ID_26334910,Human_RBP_ID_26815805 Human_Splice_Rec_2003488,Human_Splice_Rec_2003514,Human_Splice_Rec_2003536,Human_Splice_Rec_2003572 Human_miRNA_ID_1987185,Human_miRNA_ID_3123702 RMVar_hsa_circ_194638,RMVar_hsa_circ_77110,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_194651,RMVar_hsa_circ_101860,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_89445,RMVar_hsa_circ_124372,RMVar_hsa_circ_194657,RMVar_hsa_circ_120378,RMVar_hsa_circ_194658,RMVar_hsa_circ_194660,RMVar_hsa_circ_84839,RMVar_hsa_circ_194661,RMVar_hsa_circ_194659 84214 RMVar_ID_84214 Human_SNP_ID_665335194 m1A Human chr19 + 38725878 38725878 38725878 CCAGCTCATCCAGGAGGCCCTCATCTTCGACAACAAGCACACCAACTATACCATGGAGGTGCGCG CCAGCTCATCCAGGAGGCCCTCATCTTCGACAGCAAGCACACCAACTATACCATGGAGGTGCGCG A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38725828..38727883 32194978 MeRIP-seq:(Medium) rs751899053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9259012,Human_RBP_ID_9380979,Human_RBP_ID_18441253,Human_RBP_ID_18532443,Human_RBP_ID_24484272 Human_Splice_Rec_2003491,Human_Splice_Rec_2003517,Human_Splice_Rec_2003539,Human_Splice_Rec_2003575 Human_miRNA_ID_2237782 RMVar_hsa_circ_194638,RMVar_hsa_circ_77110,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_194651,RMVar_hsa_circ_101860,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_89445,RMVar_hsa_circ_124372,RMVar_hsa_circ_194657,RMVar_hsa_circ_120378,RMVar_hsa_circ_194658,RMVar_hsa_circ_67106,RMVar_hsa_circ_194660,RMVar_hsa_circ_194661,RMVar_hsa_circ_42055 84215 RMVar_ID_84215 Human_SNP_ID_665336433 m1A Human chr19 + 38729326 38729326 38729326 GCTGCGGAGAGAGCTGCCCCCCGACCAGGCCGAGTACTGCATCGCCCGCATGGCGCCATACCAGG GCTGCGGAGAGAGCTGCCCCCCGACCAGGCCGGGTACTGCATCGCCCGCATGGCGCCATACCAGG A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:38729301..38729325;chr19:38729251..38729325 26863196 MeRIP-seq:(Medium) rs945344270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5145195,Human_RBP_ID_6759851,Human_RBP_ID_8486602,Human_RBP_ID_8833572,Human_RBP_ID_22446711,Human_RBP_ID_22533396,Human_RBP_ID_22764077,Human_RBP_ID_24484274,Human_RBP_ID_26989417 Human_Splice_Rec_2003498,Human_Splice_Rec_2003524,Human_Splice_Rec_2003546,Human_Splice_Rec_2003582,Human_Splice_Rec_2003586,Human_Splice_Rec_2003590 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 84216 RMVar_ID_84216 Human_SNP_ID_665336461 m1A Human chr19 - 38729378 38729378 38729378 AAGGCCGTGGAGAAGGACTTGTAGTCGAGGGCACCGGGCACGGCGTCAGGGCCCTGGTATGGCGC AAGGCCGTGGAGAAGGACTTGTAGTCGAGGGCCCCGGGCACGGCGTCAGGGCCCTGGTATGGCGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38729327..38729550 26863196 MeRIP-seq:(Medium) rs1330055694 Functional Loss SNV dbSNP153 33..33 33 - - - 84217 RMVar_ID_84217 Human_SNP_ID_665336465 m1A Human chr19 - 38729394 38729394 38729394 GTCGCTCTCGCCATACAAGGCCGTGGAGAAGGACTTGTAGTCGAGGGCACCGGGCACGGCGTCAG GTCGCTCTCGCCATACAAGGCCGTGGAGAAGGTCTTGTAGTCGAGGGCACCGGGCACGGCGTCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38729343..38729494 26863196 MeRIP-seq:(Medium) rs748619848 Functional Loss SNV dbSNP153 33..33 33 - - - 84218 RMVar_ID_84218 Human_SNP_ID_665336494 m1A Human chr19 + 38729453 38729453 38729453 AGCGACCTGTGAGGCCCCAGAGACCTGACCCAACACCCCCGACGGCCTCCAGGAGGGGCCTGGGC AGCGACCTGTGAGGCCCCAGAGACCTGACCCAGCACCCCCGACGGCCTCCAGGAGGGGCCTGGGC A G ACTN4 Ensembl:ENSG00000130402 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38729290..38729550 26863196 MeRIP-seq:(Medium) rs755767012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53996,Human_RBP_ID_1189512,Human_RBP_ID_6759857,Human_RBP_ID_17657025,Human_RBP_ID_22446712,Human_RBP_ID_22502697 Human_miRNA_ID_1091033 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 84219 RMVar_ID_84219 Human_SNP_ID_665336632 m1A Human chr19 - 38729675 38729675 38729675 GCCCCTCCTTGGTTAAAAAAGCACAACACATCATACATATTTACCAGACCAGAAGCGCTGGCCCC GCCCCTCCTTGGTTAAAAAAGCACAACACATCGTACATATTTACCAGACCAGAAGCGCTGGCCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:38729651..38729675 26863196 MeRIP-seq:(Medium) rs1032290348 Functional Loss SNV dbSNP153 33..33 33 - - - 84220 RMVar_ID_84220 Human_SNP_ID_665336666 m1A Human chr19 + 38729797 38729797 38729797 CCAGGTCTCTTCCTTTGCTCTGAGGTCCCTTCAAGGCCTCCCCAATCCAGGCCAAAGCCCCATGT CCAGGTCTCTTCCTTTGCTCTGAGGTCCCTTCCAGGCCTCCCCAATCCAGGCCAAAGCCCCATGT A C ACTN4 Ensembl:ENSG00000130402 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38729776..38729800 26863196 MeRIP-seq:(Medium) rs1257437389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53999,Human_RBP_ID_521181,Human_RBP_ID_1189519,Human_RBP_ID_1564151,Human_RBP_ID_8486614,Human_RBP_ID_17383973,Human_RBP_ID_17499807,Human_RBP_ID_17695568,Human_RBP_ID_17924078,Human_RBP_ID_18192232,Human_RBP_ID_23210946,Human_RBP_ID_24484282,Human_RBP_ID_26472459 Human_miRNA_ID_109714,Human_miRNA_ID_837248,Human_miRNA_ID_1966646,Human_miRNA_ID_2362105,Human_miRNA_ID_2368294,Human_miRNA_ID_3016077 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 84221 RMVar_ID_84221 Human_SNP_ID_665336719 m1A Human chr19 - 38729940 38729940 38729940 GTGCTTGTTGGGGCCATCTCCTGGCAATGGCAAGTGAGTCTGGAGCAGAGAGGGGAGAGGGGCTG GTGCTTGTTGGGGCCATCTCCTGGCAATGGCAGGTGAGTCTGGAGCAGAGAGGGGAGAGGGGCTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:38729601..38730026 26863196 MeRIP-seq:(Medium) rs1360518984 Functional Loss SNV dbSNP153 33..33 33 - - - 84222 RMVar_ID_84222 Human_SNP_ID_665336723 m1A Human chr19 + 38729951 38729951 38729951 CCCTCTCTGCTCCAGACTCACTTGCCATTGCCAGGAGATGGCCCCAACAAGCACCCCGCTTTTGC CCCTCTCTGCTCCAGACTCACTTGCCATTGCCGGGAGATGGCCCCAACAAGCACCCCGCTTTTGC A G ACTN4 Ensembl:ENSG00000130402 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38729586..38730031 26863196 MeRIP-seq:(Medium) rs1172750355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521183,Human_RBP_ID_1015693,Human_RBP_ID_3571318,Human_RBP_ID_4526065,Human_RBP_ID_6759869,Human_RBP_ID_8486616,Human_RBP_ID_17657031,Human_RBP_ID_17924079,Human_RBP_ID_18731757,Human_RBP_ID_23796476,Human_RBP_ID_24484289,Human_RBP_ID_26472461 Human_miRNA_ID_254481 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 84223 RMVar_ID_84223 Human_SNP_ID_665336979 m1A Human chr19 + 38730300 38730300 38730300 TCTCTCCTGCTCTCATAATGAAGACATAGCCGATTCTCTGCCCGGGCCCCTTGCTGATGCTCCTC TCTCTCCTGCTCTCATAATGAAGACATAGCCGGTTCTCTGCCCGGGCCCCTTGCTGATGCTCCTC A G ACTN4 Ensembl:ENSG00000130402 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38730205..38730370 26863196 MeRIP-seq:(Medium) rs1012720237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54003,Human_RBP_ID_521190,Human_RBP_ID_1015698,Human_RBP_ID_1239956,Human_RBP_ID_1294156,Human_RBP_ID_1373204,Human_RBP_ID_1564156,Human_RBP_ID_1887080,Human_RBP_ID_3571320,Human_RBP_ID_4526077,Human_RBP_ID_5116241,Human_RBP_ID_6759880,Human_RBP_ID_8486623,Human_RBP_ID_8833581,Human_RBP_ID_9292121,Human_RBP_ID_13450331,Human_RBP_ID_17268883,Human_RBP_ID_17383977,Human_RBP_ID_17499812,Human_RBP_ID_17657033,Human_RBP_ID_17695570,Human_RBP_ID_18304979,Human_RBP_ID_22971852,Human_RBP_ID_23177633,Human_RBP_ID_24418715,Human_RBP_ID_24484296,Human_RBP_ID_27273805,Human_RBP_ID_27467732,Human_RBP_ID_27679689 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 84224 RMVar_ID_84224 Human_SNP_ID_665339936 m1A Human chr19 - 38736085 38736085 38736085 ACGGCCGTGTGAGCCCCGGGCACCCAAATCCGACCCCATCCCTGCCTAGACAGGCCCCGAGACCC ACGGCCGTGTGAGCCCCGGGCACCCAAATCCGGCCCCATCCCTGCCTAGACAGGCCCCGAGACCC T C CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38736054..38736188 26863196 MeRIP-seq:(Medium) rs1230291538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911318 84225 RMVar_ID_84225 Human_SNP_ID_665340395 m1A Human chr19 + 38736618 38736618 38736618 GCGTCGGGGCAGGGGAGAGGTGGCCGCCGCTCAGGGTCTCCTCCCTGCCCCTTCTCACCTCTGTG GCGTCGGGGCAGGGGAGAGGTGGCCGCCGCTCGGGGTCTCCTCCCTGCCCCTTCTCACCTCTGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38736582..38736790 26863196 MeRIP-seq:(Medium) rs1460543262 Functional Loss SNV dbSNP153 33..33 33 - - - 84226 RMVar_ID_84226 Human_SNP_ID_665340425 m1A Human chr19 + 38736715 38736715 38736715 TTATTGAACCTTTGCCCCGCAGTCCCCGACCCAGGCCCTCGCCGACCCCTCCCCAACTCTTCCTT TTATTGAACCTTTGCCCCGCAGTCCCCGACCCTGGCCCTCGCCGACCCCTCCCCAACTCTTCCTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38736708..38736799 26863196 MeRIP-seq:(Medium) rs1463154579 Functional Loss SNV dbSNP153 33..33 33 - - - 84227 RMVar_ID_84227 Human_SNP_ID_665340458 m1A Human chr19 - 38736816 38736789 38736816 GGACAGACAGAGGGACGAGGTTAGGGACAGAGAGAGGCTGGGGGTTAGAAGGGCCAGAGGGGACC GGACAGACAGAGGGACGAGGTTAGGGACAGAG___________________________GGGACC CCTCTGGCCCTTCTAACCCCCAGCCTCT C CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38736671..38736970 26863196 MeRIP-seq:(Medium) rs1191164591 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_3581176,Human_RBP_ID_5320347,Human_RBP_ID_8196449,Human_RBP_ID_8942214,Human_RBP_ID_9425310,Human_RBP_ID_9929733,Human_RBP_ID_18421371,Human_RBP_ID_21979232,Human_RBP_ID_26472467 84228 RMVar_ID_84228 Human_SNP_ID_665340470 m1A Human chr19 - 38736816 38736812 38736816 GGACAGACAGAGGGACGAGGTTAGGGACAGAGAGAGGCTGGGGGTTAGAAGGGCCAGAGGGGACC GGACAGACAGAGGGACGAGGTTAGGGACAGAG____GCTGGGGGTTAGAAGGGCCAGAGGGGACC CCTCT C CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38736671..38736970 26863196 MeRIP-seq:(Medium) rs537026543 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3581176,Human_RBP_ID_5320347,Human_RBP_ID_8196449,Human_RBP_ID_8942214,Human_RBP_ID_9425310,Human_RBP_ID_9929733,Human_RBP_ID_18421371,Human_RBP_ID_21979232,Human_RBP_ID_26472467 84229 RMVar_ID_84229 Human_SNP_ID_665340471 m1A Human chr19 - 38736816 38736812 38736816 GGACAGACAGAGGGACGAGGTTAGGGACAGAGAGAGGCTGGGGGTTAGAAGGGCCAGAGGGGACC GGACAGACAGAGGGACGAGGTTAGGGACAGAG__AGGCTGGGGGTTAGAAGGGCCAGAGGGGACC CCTCT CCT CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38736671..38736970 26863196 MeRIP-seq:(Medium) rs537026543 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3581176,Human_RBP_ID_5320347,Human_RBP_ID_8196449,Human_RBP_ID_8942214,Human_RBP_ID_9425310,Human_RBP_ID_9929733,Human_RBP_ID_18421371,Human_RBP_ID_21979232,Human_RBP_ID_26472467 84230 RMVar_ID_84230 Human_SNP_ID_665341028 m1A Human chr19 - 38737871 38737871 38737871 GGGTCTTGCTATTTGGGGGTTGGTGGCAATTTAACGATATTTGGGGGCAGCTTGTGAATCTTGGC GGGTCTTGCTATTTGGGGGTTGGTGGCAATTTGACGATATTTGGGGGCAGCTTGTGAATCTTGGC T C CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38737830..38737980 26863196 MeRIP-seq:(Medium) rs1243144278 Functional Loss SNV dbSNP153 33..33 33 - - - 84231 RMVar_ID_84231 Human_SNP_ID_665363331 m1A Human chr19 + 38815960 38815960 38815960 CCACGGGGCTCTTGCTGGAAATCTCGGCCGCCAGCGCTAAGGCAGCATCCAGCATGACCTCTTTG CCACGGGGCTCTTGCTGGAAATCTCGGCCGCCGGCGCTAAGGCAGCATCCAGCATGACCTCTTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38815501..38816054 32194978 MeRIP-seq:(Medium) rs778594450 Functional Loss SNV dbSNP153 33..33 33 - - - 84232 RMVar_ID_84232 Human_SNP_ID_665363711 m1A Human chr19 + 38817056 38817056 38817056 CACTGCCCAGCTCTAAGCAGGAGCTCGGGAGGATGACTCACCTTCACCTGGAAGAAAGCATCCTG CACTGCCCAGCTCTAAGCAGGAGCTCGGGAGGCTGACTCACCTTCACCTGGAAGAAAGCATCCTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38817054..38817154 32194978 MeRIP-seq:(Medium) rs769343039 Functional Loss SNV dbSNP153 33..33 33 - - - 84233 RMVar_ID_84233 Human_SNP_ID_665367711 m1A Human chr19 - 38831146 38831146 38831146 GTTGCTTCACAGAGAGATGGTAGAGTGCTTCAACAAGATTTCGAGAGACGCTGACTGTCGGGCGG GTTGCTTCACAGAGAGATGGTAGAGTGCTTCAGCAAGATTTCGAGAGACGCTGACTGTCGGGCGG T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38831051..38831212 26863196 MeRIP-seq:(Medium) rs770996341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52961,Human_RBP_ID_17934978,Human_RBP_ID_18997710 Human_Splice_Rec_2003842,Human_Splice_Rec_2003843,Human_Splice_Rec_2003868,Human_Splice_Rec_2003869,Human_Splice_Rec_2003882,Human_Splice_Rec_2003883,Human_Splice_Rec_2003896,Human_Splice_Rec_2003897,Human_Splice_Rec_2003908,Human_Splice_Rec_2003909,Human_Splice_Rec_2003914,Human_Splice_Rec_2003915,Human_Splice_Rec_2003922,Human_Splice_Rec_2003923,Human_Splice_Rec_2003930,Human_Splice_Rec_2003931,Human_Splice_Rec_2003936,Human_Splice_Rec_2003938,Human_Splice_Rec_2003940,Human_Splice_Rec_2003942,Human_Splice_Rec_2003944,Human_Splice_Rec_2003948,Human_Splice_Rec_2003962,Human_Splice_Rec_2003963 Human_miRNA_ID_2977863 RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 84234 RMVar_ID_84234 Human_SNP_ID_665367847 m1A Human chr19 - 38831414 38831414 38831414 GGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGACCACAGCTATGAGTCCCTTCGTGTGACGTCTG GGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGCCCACAGCTATGAGTCCCTTCGTGTGACGTCTG T G AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38831363..38831512 32194978 MeRIP-seq:(Medium) rs1408831825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770489,Human_RBP_ID_825575,Human_RBP_ID_1564173,Human_RBP_ID_1887091,Human_RBP_ID_4567855,Human_RBP_ID_8486653,Human_RBP_ID_8839344,Human_RBP_ID_18731783,Human_RBP_ID_22446719 Human_Splice_Rec_2003937 RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 84235 RMVar_ID_84235 Human_SNP_ID_665367850 m1A Human chr19 - 38831416 38831416 38831416 GAGGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGACCACAGCTATGAGTCCCTTCGTGTGACGTC GAGGCTTCCGGAGTAGCCCTCGGTGAAGCCCCGGACCACAGCTATGAGTCCCTTCGTGTGACGTC T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:38831369..38831525 26863196 MeRIP-seq:(Medium) rs149384635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770489,Human_RBP_ID_825575,Human_RBP_ID_1564173,Human_RBP_ID_1887091,Human_RBP_ID_4567855,Human_RBP_ID_8486653,Human_RBP_ID_8839344,Human_RBP_ID_18731783,Human_RBP_ID_22448692 Human_Splice_Rec_2003937 RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 84236 RMVar_ID_84236 Human_SNP_ID_665367851 m1A Human chr19 - 38831416 38831416 38831416 GAGGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGACCACAGCTATGAGTCCCTTCGTGTGACGTC GAGGCTTCCGGAGTAGCCCTCGGTGAAGCCCCCGACCACAGCTATGAGTCCCTTCGTGTGACGTC T G AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:38831369..38831525 26863196 MeRIP-seq:(Medium) rs149384635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770489,Human_RBP_ID_825575,Human_RBP_ID_1564173,Human_RBP_ID_1887091,Human_RBP_ID_4567855,Human_RBP_ID_8486653,Human_RBP_ID_8839344,Human_RBP_ID_18731783,Human_RBP_ID_22448692 Human_Splice_Rec_2003937 RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 84237 RMVar_ID_84237 Human_SNP_ID_665367987 m1A Human chr19 + 38831702 38831702 38831702 TATAACAGCACGACAGCGCGACGCACCCCCATAAGGCAAGAGGTGACTCACGCCGGGTCAGTAGG TATAACAGCACGACAGCGCGACGCACCCCCATGAGGCAAGAGGTGACTCACGCCGGGTCAGTAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:38831701..38831775;chr19:38831701..38831800 26863196 MeRIP-seq:(Medium) rs931087608 Functional Loss SNV dbSNP153 33..33 33 - - - 84238 RMVar_ID_84238 Human_SNP_ID_665369527 m1A Human chr19 - 38836537 38836537 38836537 CCTTAATGGAAACGCTGGAAATCTGCAGGGGGAGGGAGAGGGGAACTGTTATCTCCCAAGATTAA CCTTAATGGAAACGCTGGAAATCTGCAGGGGGGGGGAGAGGGGAACTGTTATCTCCCAAGATTAA T C AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:38836487..38836587 32194978 MeRIP-seq:(Medium) rs1478060173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239442,Human_RBP_ID_521222,Human_RBP_ID_770490,Human_RBP_ID_1564180,Human_RBP_ID_1887094,Human_RBP_ID_2565145,Human_RBP_ID_3571344,Human_RBP_ID_5116243,Human_RBP_ID_5145200,Human_RBP_ID_6759944,Human_RBP_ID_8486665,Human_RBP_ID_13450505,Human_RBP_ID_17068332,Human_RBP_ID_17657040,Human_RBP_ID_18731793,Human_RBP_ID_20349376,Human_RBP_ID_22810664,Human_RBP_ID_22971860,Human_RBP_ID_23131148,Human_RBP_ID_23210950,Human_RBP_ID_23796500,Human_RBP_ID_24420049,Human_RBP_ID_24484315,Human_RBP_ID_26474905 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_194675 84239 RMVar_ID_84239 Human_SNP_ID_665369639 m1A Human chr19 + 38836776 38836776 38836776 GAGAAACACAACTTCAGAGTGTAAGGGTATGGACCATCTGCAAAGGAGAGACAAGTTTGGTTGGT GAGAAACACAACTTCAGAGTGTAAGGGTATGGGCCATCTGCAAAGGAGAGACAAGTTTGGTTGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38836727..38836815 26863196 MeRIP-seq:(Medium) rs1461394671 Functional Loss SNV dbSNP153 33..33 33 - - - 84240 RMVar_ID_84240 Human_SNP_ID_665369727 m1A Human chr19 + 38836989 38836989 38836989 CCTTCTCTTCCTTCATTCCCATAGAGAATCCCATTCCTATCTCCTTCGCCAGCCCAAGGCAATGG CCTTCTCTTCCTTCATTCCCATAGAGAATCCCTTTCCTATCTCCTTCGCCAGCCCAAGGCAATGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38836984..38837334 32194978 MeRIP-seq:(Medium) rs1352553215 Functional Loss SNV dbSNP153 33..33 33 - - - 84241 RMVar_ID_84241 Human_SNP_ID_665369864 m1A Human chr19 - 38837425 38837425 38837425 GCTGGAGTGGGAATCCAAGAGCGATGCCCTGGAGACTCTGGGCTTCCTGAACCATTACCAGATGA GCTGGAGTGGGAATCCAAGAGCGATGCCCTGGGGACTCTGGGCTTCCTGAACCATTACCAGATGA T C AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38837376..38837425 32194978 MeRIP-seq:(Medium) rs1015279604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521233,Human_RBP_ID_770491,Human_RBP_ID_911322,Human_RBP_ID_1015721,Human_RBP_ID_1564208,Human_RBP_ID_1887104,Human_RBP_ID_3571351,Human_RBP_ID_6759980,Human_RBP_ID_8486675,Human_RBP_ID_9293666,Human_RBP_ID_13450541,Human_RBP_ID_17268897,Human_RBP_ID_17499825,Human_RBP_ID_17924111,Human_RBP_ID_18731804,Human_RBP_ID_22446722,Human_RBP_ID_22977916 Human_Splice_Rec_2003958,Human_Splice_Rec_2003959,Human_Splice_Rec_2003968,Human_Splice_Rec_2003969,Human_Splice_Rec_2003988,Human_Splice_Rec_2003989,Human_Splice_Rec_2004010,Human_Splice_Rec_2004011,Human_Splice_Rec_2004018,Human_Splice_Rec_2004019,Human_Splice_Rec_2004040,Human_Splice_Rec_2004041,Human_Splice_Rec_2004064,Human_Splice_Rec_2004065,Human_Splice_Rec_2004076,Human_Splice_Rec_2004077,Human_Splice_Rec_2004086,Human_Splice_Rec_2004087,Human_Splice_Rec_2004108,Human_Splice_Rec_2004109 Human_miRNA_ID_3004861 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194675,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676 84242 RMVar_ID_84242 Human_SNP_ID_665369870 m1A Human chr19 - 38837441 38837441 38837441 GCAGCTCCTCTGGACTGCTGGAGTGGGAATCCAAGAGCGATGCCCTGGAGACTCTGGGCTTCCTG GCAGCTCCTCTGGACTGCTGGAGTGGGAATCCCAGAGCGATGCCCTGGAGACTCTGGGCTTCCTG T G AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38837376..38837450 32194978 MeRIP-seq:(Medium) rs1568366146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521233,Human_RBP_ID_770491,Human_RBP_ID_1564210,Human_RBP_ID_1887104,Human_RBP_ID_3571351,Human_RBP_ID_4567876,Human_RBP_ID_6759980,Human_RBP_ID_8486675,Human_RBP_ID_8833596,Human_RBP_ID_9087744,Human_RBP_ID_9293666,Human_RBP_ID_13450541,Human_RBP_ID_17268898,Human_RBP_ID_22447739,Human_RBP_ID_22977916,Human_RBP_ID_25445736 Human_Splice_Rec_2003958,Human_Splice_Rec_2003959,Human_Splice_Rec_2003968,Human_Splice_Rec_2003969,Human_Splice_Rec_2003988,Human_Splice_Rec_2003989,Human_Splice_Rec_2004010,Human_Splice_Rec_2004011,Human_Splice_Rec_2004018,Human_Splice_Rec_2004019,Human_Splice_Rec_2004040,Human_Splice_Rec_2004041,Human_Splice_Rec_2004064,Human_Splice_Rec_2004065,Human_Splice_Rec_2004076,Human_Splice_Rec_2004077,Human_Splice_Rec_2004086,Human_Splice_Rec_2004087,Human_Splice_Rec_2004108,Human_Splice_Rec_2004109 Human_miRNA_ID_2696266 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194675,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676 84243 RMVar_ID_84243 Human_SNP_ID_665369871 m1A Human chr19 - 38837441 38837441 38837441 GCAGCTCCTCTGGACTGCTGGAGTGGGAATCCAAGAGCGATGCCCTGGAGACTCTGGGCTTCCTG GCAGCTCCTCTGGACTGCTGGAGTGGGAATCCGAGAGCGATGCCCTGGAGACTCTGGGCTTCCTG T C AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38837376..38837450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_521233,Human_RBP_ID_770491,Human_RBP_ID_1564210,Human_RBP_ID_1887104,Human_RBP_ID_3571351,Human_RBP_ID_4567876,Human_RBP_ID_6759980,Human_RBP_ID_8486675,Human_RBP_ID_8833596,Human_RBP_ID_9087744,Human_RBP_ID_9293666,Human_RBP_ID_13450541,Human_RBP_ID_17268898,Human_RBP_ID_22447739,Human_RBP_ID_22977916,Human_RBP_ID_25445736 Human_Splice_Rec_2003958,Human_Splice_Rec_2003959,Human_Splice_Rec_2003968,Human_Splice_Rec_2003969,Human_Splice_Rec_2003988,Human_Splice_Rec_2003989,Human_Splice_Rec_2004010,Human_Splice_Rec_2004011,Human_Splice_Rec_2004018,Human_Splice_Rec_2004019,Human_Splice_Rec_2004040,Human_Splice_Rec_2004041,Human_Splice_Rec_2004064,Human_Splice_Rec_2004065,Human_Splice_Rec_2004076,Human_Splice_Rec_2004077,Human_Splice_Rec_2004086,Human_Splice_Rec_2004087,Human_Splice_Rec_2004108,Human_Splice_Rec_2004109 Human_miRNA_ID_2696266 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194675,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676 84244 RMVar_ID_84244 Human_SNP_ID_665370215 m1A Human chr19 + 38838419 38838419 38838419 CGGCACACACCTCAAAGAAGTTCTCCTCGGTCACCTCCAGCGGGGCGTTGAAGAAGTGCAGCACG CGGCACACACCTCAAAGAAGTTCTCCTCGGTCGCCTCCAGCGGGGCGTTGAAGAAGTGCAGCACG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38837582..38838514 32194978 MeRIP-seq:(Medium) rs770290428 Functional Loss SNV dbSNP153 33..33 33 - - - 84245 RMVar_ID_84245 Human_SNP_ID_665370844 m1A Human chr19 - 38840213 38840213 38840213 CAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCACGCCGACAGCCCTGT CAGTATGGGCACCCCCCACCCCCTCCCCCACCTCCCGAGTATGGCCCTCACGCCGACAGCCCTGT T A HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38840163..38840263 32194978 MeRIP-seq:(Medium) rs752851856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84246 RMVar_ID_84246 Human_SNP_ID_665370845 m1A Human chr19 - 38840213 38840213 38840213 CAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCACGCCGACAGCCCTGT CAGTATGGGCACCCCCCACCCCCTCCCCCACCGCCCGAGTATGGCCCTCACGCCGACAGCCCTGT T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38840163..38840263 32194978 MeRIP-seq:(Medium) rs752851856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84247 RMVar_ID_84247 Human_SNP_ID_665370846 m1A Human chr19 - 38840213 38840213 38840213 CAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCACGCCGACAGCCCTGT CAGTATGGGCACCCCCCACCCCCTCCCCCACCCCCCGAGTATGGCCCTCACGCCGACAGCCCTGT T G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38840163..38840263 32194978 MeRIP-seq:(Medium) rs752851856 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84248 RMVar_ID_84248 Human_SNP_ID_665370847 m1A Human chr19 - 38840216 38840216 38840216 CCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCACGCCGACAGCCC CCCCAGTATGGGCACCCCCCACCCCCTCCCCCCCCACCCGAGTATGGCCCTCACGCCGACAGCCC T G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1441410370 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84249 RMVar_ID_84249 Human_SNP_ID_665370851 m1A Human chr19 + 38840222 38840221 38840222 TCGGCGTGAGGGCCATACTCGGGTGGTGGGGGAGGGGGTGGGGGGTGCCCATACTGGGGGCCGTA TCGGCGTGAGGGCCATACTCGGGTGGTGGGGG_GGGGGTGGGGGGTGCCCATACTGGGGGCCGTA GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:38840201..38840225;chr19:38840176..38840225 26863196 MeRIP-seq:(Medium) rs1228299246 Functional Loss DEL dbSNP153 33..33 33 - - - 84250 RMVar_ID_84250 Human_SNP_ID_665370852 m1A Human chr19 + 38840222 38840222 38840222 TCGGCGTGAGGGCCATACTCGGGTGGTGGGGGAGGGGGTGGGGGGTGCCCATACTGGGGGCCGTA TCGGCGTGAGGGCCATACTCGGGTGGTGGGGGGGGGGGTGGGGGGTGCCCATACTGGGGGCCGTA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:38840201..38840225;chr19:38840176..38840225 26863196 MeRIP-seq:(Medium) rs747010552 Functional Loss SNV dbSNP153 33..33 33 - - - 84251 RMVar_ID_84251 Human_SNP_ID_665370856 m1A Human chr19 - 38840228 38840226 38840228 AGTCGCTACGGCCCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCA AGTCGCTACGGCCCCCAGTATGGGCACCCCCC__CCCCTCCCCCACCACCCGAGTATGGCCCTCA GGT G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1298871667 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1560578,Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84252 RMVar_ID_84252 Human_SNP_ID_665370859 m1A Human chr19 - 38840228 38840227 38840228 AGTCGCTACGGCCCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCA AGTCGCTACGGCCCCCAGTATGGGCACCCCCC_CCCCCTCCCCCACCACCCGAGTATGGCCCTCA GT G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1344721703 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_1560578,Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84253 RMVar_ID_84253 Human_SNP_ID_665370860 m1A Human chr19 - 38840228 38840228 38840228 AGTCGCTACGGCCCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCA AGTCGCTACGGCCCCCAGTATGGGCACCCCCCCCCCCCTCCCCCACCACCCGAGTATGGCCCTCA T G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs757247424 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1560578,Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84254 RMVar_ID_84254 Human_SNP_ID_665370925 m1A Human chr19 - 38840353 38840353 38840353 ACCCCCCAGGAGGGCCCCACGGTGGGTACCACAGCCATTACCATGATGAGGGCTACGGGCCCCCC ACCCCCCAGGAGGGCCCCACGGTGGGTACCACGGCCATTACCATGATGAGGGCTACGGGCCCCCC T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:38840351..38840375 26863196 MeRIP-seq:(Medium) rs1333989786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52966,Human_RBP_ID_239446,Human_RBP_ID_770496,Human_RBP_ID_913624,Human_RBP_ID_9330017,Human_RBP_ID_17655612,Human_RBP_ID_18441263,Human_RBP_ID_22234537,Human_RBP_ID_22446729,Human_RBP_ID_24484328 Human_Splice_Rec_2004002,Human_Splice_Rec_2004032,Human_Splice_Rec_2004056,Human_Splice_Rec_2004068,Human_Splice_Rec_2004100 Human_miRNA_ID_2277219 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 84255 RMVar_ID_84255 Human_SNP_ID_665371076 m1A Human chr19 - 38840660 38840660 38840660 GCCCCACAGCCCTCGAGGAAGGGAGGGCTTGCAGTTGGCAGGAGCTGGGGGCTCAGATCAGCCTG GCCCCACAGCCCTCGAGGAAGGGAGGGCTTGCGGTTGGCAGGAGCTGGGGGCTCAGATCAGCCTG T C HNRNPL Ensembl:ENSG00000104824 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38840611..38840960 32194978 MeRIP-seq:(Medium) rs1293210803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6760049 Human_miRNA_ID_2469989 RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_103339,RMVar_hsa_circ_194680 84256 RMVar_ID_84256 Human_SNP_ID_665372211 m1A Human chr19 + 38844266 38844266 38844266 CTGCCCAGCCACTAGCCTCAGGTTAAGAGACCAAAACGGTGTTGATGGACTCAACGCTGCCCCGG CTGCCCAGCCACTAGCCTCAGGTTAAGAGACCGAAACGGTGTTGATGGACTCAACGCTGCCCCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38844263..38844655 26863196 MeRIP-seq:(Medium) rs1388531251 Functional Loss SNV dbSNP153 33..33 33 - - - 84257 RMVar_ID_84257 Human_SNP_ID_665372325 m1A Human chr19 - 38844592 38844592 38844592 AAGGTTGTAAAGTCAGAAGGAGCTTGTGTTGGATGGAGAAATTGAAAGACCTGAGGATTGCAAAG AAGGTTGTAAAGTCAGAAGGAGCTTGTGTTGGGTGGAGAAATTGAAAGACCTGAGGATTGCAAAG T C HNRNPL Ensembl:ENSG00000104824 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38844590..38844666 26863196 MeRIP-seq:(Medium) rs568321843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1564339,Human_RBP_ID_6760161,Human_RBP_ID_9921058,Human_RBP_ID_13450815,Human_RBP_ID_22971993,Human_RBP_ID_23796530,Human_RBP_ID_27679708 RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_313839,RMVar_hsa_circ_322096,RMVar_hsa_circ_117856,RMVar_hsa_circ_194682,RMVar_hsa_circ_194683 84258 RMVar_ID_84258 Human_SNP_ID_665372861 m1A Human chr19 - 38846018 38846018 38846018 GAGTTTGAAGATGTGTTGGGGGCTTGCAACGCAGTGAACTACGCAGCCGACAACCAAATATACAT GAGTTTGAAGATGTGTTGGGGGCTTGCAACGCGGTGAACTACGCAGCCGACAACCAAATATACAT T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38845976..38846050 26863196 MeRIP-seq:(Medium) rs746203577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1564354,Human_RBP_ID_1887165,Human_RBP_ID_3571382,Human_RBP_ID_4526251,Human_RBP_ID_8486741,Human_RBP_ID_8840023,Human_RBP_ID_9087758,Human_RBP_ID_9380984,Human_RBP_ID_13450854,Human_RBP_ID_17695579,Human_RBP_ID_18731894,Human_RBP_ID_22070173,Human_RBP_ID_22448703,Human_RBP_ID_23796537,Human_RBP_ID_26334914,Human_RBP_ID_26815838,Human_RBP_ID_26989518,Human_RBP_ID_27273843 Human_Splice_Rec_2003974,Human_Splice_Rec_2003994,Human_Splice_Rec_2004024,Human_Splice_Rec_2004046,Human_Splice_Rec_2004092,Human_Splice_Rec_2004116,Human_Splice_Rec_2004126,Human_Splice_Rec_2004134,Human_Splice_Rec_2004142,Human_Splice_Rec_2004146 RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_58914,RMVar_hsa_circ_313839,RMVar_hsa_circ_322096,RMVar_hsa_circ_194683,RMVar_hsa_circ_194684,RMVar_hsa_circ_372195,RMVar_hsa_circ_194685 84259 RMVar_ID_84259 Human_SNP_ID_665372869 m1A Human chr19 + 38846037 38846037 38846037 CTGCGTAGTTCACTGCGTTGCAAGCCCCCAACACATCTTCAAACTCCACCAGTGCTTGTCTCTTT CTGCGTAGTTCACTGCGTTGCAAGCCCCCAACGCATCTTCAAACTCCACCAGTGCTTGTCTCTTT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:38845851..38846144 26863410 MeRIP-seq:(Medium) rs1305949412 Functional Loss SNV dbSNP153 33..33 33 - - - 84260 RMVar_ID_84260 Human_SNP_ID_665373318 m1A Human chr19 + 38847372 38847372 38847372 GCCTCCACAAGGTCTGCTTCCACCACACCGTCAATCAGGCCCCTGATGTGGACAACTGGGGAGGC GCCTCCACAAGGTCTGCTTCCACCACACCGTCTATCAGGCCCCTGATGTGGACAACTGGGGAGGC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38847301..38847425 32194978 MeRIP-seq:(Medium) rs1278641816 Functional Loss SNV dbSNP153 33..33 33 - - - 84261 RMVar_ID_84261 Human_SNP_ID_665373319 m1A Human chr19 - 38847374 38847374 38847374 CTGCCTCCCCAGTTGTCCACATCAGGGGCCTGATTGACGGTGTGGTGGAAGCAGACCTTGTGGAG CTGCCTCCCCAGTTGTCCACATCAGGGGCCTGGTTGACGGTGTGGTGGAAGCAGACCTTGTGGAG T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38847301..38847450 32194978 MeRIP-seq:(Medium) rs764828228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55002,Human_RBP_ID_1015736,Human_RBP_ID_1564362,Human_RBP_ID_1887170,Human_RBP_ID_3571384,Human_RBP_ID_3954979,Human_RBP_ID_4526257,Human_RBP_ID_6760215,Human_RBP_ID_8486746,Human_RBP_ID_8833614,Human_RBP_ID_9293672,Human_RBP_ID_9330018,Human_RBP_ID_18441267,Human_RBP_ID_18731901,Human_RBP_ID_22446733,Human_RBP_ID_23114776,Human_RBP_ID_23796540 Human_Splice_Rec_2003973,Human_Splice_Rec_2003992,Human_Splice_Rec_2003993,Human_Splice_Rec_2004022,Human_Splice_Rec_2004023,Human_Splice_Rec_2004044,Human_Splice_Rec_2004045,Human_Splice_Rec_2004090,Human_Splice_Rec_2004091,Human_Splice_Rec_2004114,Human_Splice_Rec_2004115,Human_Splice_Rec_2004124,Human_Splice_Rec_2004125,Human_Splice_Rec_2004132,Human_Splice_Rec_2004133,Human_Splice_Rec_2004140,Human_Splice_Rec_2004141,Human_Splice_Rec_2004145 RMVar_hsa_circ_69090,RMVar_hsa_circ_58914,RMVar_hsa_circ_313839,RMVar_hsa_circ_194683,RMVar_hsa_circ_194684,RMVar_hsa_circ_301935,RMVar_hsa_circ_194686 84262 RMVar_ID_84262 Human_SNP_ID_665373335 m1A Human chr19 - 38847433 38847431 38847434 AAATAATTCTTGTTTTTGCTTCCTTTCTCAGGAGAACTACGATGACCCGCACAAAACCCCTGCCT AAATAATTCTTGTTTTTGCTTCCTTTCTCAG___AACTACGATGACCCGCACAAAACCCCTGCCT TCTC T HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,Starvation treatment;HEK293T,untreat control;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr19:38847395..38847523;chr19:38847326..38847505;chr19:38847371..38847471;chr19:38847321..38847506;chr19:38845876..38847485;chr19:38847401..38847450 26863196,26863410,26863410,26863410,26863196,26863196 MeRIP-seq:(Medium) rs772852709 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_55002,Human_RBP_ID_1564365,Human_RBP_ID_3954979,Human_RBP_ID_5191538,Human_RBP_ID_8840024,Human_RBP_ID_9293673,Human_RBP_ID_9330019,Human_RBP_ID_22446734,Human_RBP_ID_23114776,Human_RBP_ID_25445779,Human_RBP_ID_26336233,Human_RBP_ID_26989524 Human_Splice_Rec_2003992,Human_Splice_Rec_2004022,Human_Splice_Rec_2004044,Human_Splice_Rec_2004090,Human_Splice_Rec_2004114,Human_Splice_Rec_2004124,Human_Splice_Rec_2004132,Human_Splice_Rec_2004140 Human_miRNA_ID_2077278 RMVar_hsa_circ_69090,RMVar_hsa_circ_58914,RMVar_hsa_circ_313839,RMVar_hsa_circ_194683,RMVar_hsa_circ_194684,RMVar_hsa_circ_301935,RMVar_hsa_circ_194686 84263 RMVar_ID_84263 Human_SNP_ID_665374326 m1A Human chr19 + 38849835 38849835 38849835 CCGCCCTCACTGCCGCCGCCGTAGTAGCGGCCACCGCCGCCTCCGCCGCCCGCCGCCGCCATCTT CCGCCCTCACTGCCGCCGCCGTAGTAGCGGCCGCCGCCGCCTCCGCCGCCCGCCGCCGCCATCTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:38849701..38849950 26863410 MeRIP-seq:(Medium) rs1484311732 Functional Loss SNV dbSNP153 33..33 33 - - - 84264 RMVar_ID_84264 Human_SNP_ID_665374327 m1A Human chr19 - 38849844 38849835 38849844 GCGATGGTGAAGATGGCGGCGGCGGGCGGCGGAGGCGGCGGTGGCCGCTACTACGGCGGCGGCAG GCGATGGTGAAGATGGCGGCGGCGGGCGGCGG_________TGGCCGCTACTACGGCGGCGGCAG ACCGCCGCCT A HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr19:38849638..38849975;chr19:38849650..38849950;chr19:38849687..38849925 26863196,26863410,26863410 MeRIP-seq:(Medium) rs759845330 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_55004,Human_RBP_ID_241194,Human_RBP_ID_773494,Human_RBP_ID_3956870,Human_RBP_ID_4526270,Human_RBP_ID_5320351,Human_RBP_ID_8840025,Human_RBP_ID_9328923,Human_RBP_ID_22448707,Human_RBP_ID_22533160,Human_RBP_ID_26336235 84265 RMVar_ID_84265 Human_SNP_ID_665374350 m1A Human chr19 + 38849882 38849882 38849882 GCCCGCCGCCGCCATCTTCACCATCGCTCCCGACCGCCTCCGCTGCTCGTCCGGCTGCTGCCTCT GCCCGCCGCCGCCATCTTCACCATCGCTCCCGGCCGCCTCCGCTGCTCGTCCGGCTGCTGCCTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:38849345..38850000;chr19:38849635..38849975;chr19:38849596..38850000;chr19:38849437..38850000;chr19:38849345..38850025;chr19:38849637..38849975 26863196 MeRIP-seq:(Medium) rs772828935 Functional Loss SNV dbSNP153 33..33 33 - - - 84266 RMVar_ID_84266 Human_SNP_ID_665374398 m1A Human chr19 - 38849908 38849908 38849908 GGAGAAGCGGCGTCGGCGGCTGGAGCAGAGGCAGCAGCCGGACGAGCAGCGGAGGCGGTCGGGAG GGAGAAGCGGCGTCGGCGGCTGGAGCAGAGGCGGCAGCCGGACGAGCAGCGGAGGCGGTCGGGAG T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs775793833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55004,Human_RBP_ID_3956870,Human_RBP_ID_4558415,Human_RBP_ID_5320352,Human_RBP_ID_6760291,Human_RBP_ID_8840026,Human_RBP_ID_9293674,Human_RBP_ID_9328923,Human_RBP_ID_22446736,Human_RBP_ID_22533399,Human_RBP_ID_26336235 Human_Splice_Rec_2004139 84267 RMVar_ID_84267 Human_SNP_ID_665384931 m1A Human chr19 - 38883682 38883682 38883682 GACTTGGTGGAGGCGCACGGCACCTTCTACACATCACACTGCGTCAGCGCCAGCTGCCGGCACGA GACTTGGTGGAGGCGCACGGCACCTTCTACACGTCACACTGCGTCAGCGCCAGCTGCCGGCACGA T C SIRT2 Ensembl:ENSG00000068903 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38881426..38889191 32194978 MeRIP-seq:(Medium) rs1281628438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1015742,Human_RBP_ID_3954981,Human_RBP_ID_5499531,Human_RBP_ID_17936377,Human_RBP_ID_18997714,Human_RBP_ID_26337862,Human_RBP_ID_27467761,Human_RBP_ID_27562451 Human_Splice_Rec_2004252,Human_Splice_Rec_2004253,Human_Splice_Rec_2004266,Human_Splice_Rec_2004267,Human_Splice_Rec_2004280,Human_Splice_Rec_2004281,Human_Splice_Rec_2004308,Human_Splice_Rec_2004309,Human_Splice_Rec_2004338,Human_Splice_Rec_2004339,Human_Splice_Rec_2004366,Human_Splice_Rec_2004367,Human_Splice_Rec_2004402,Human_Splice_Rec_2004403,Human_Splice_Rec_2004424,Human_Splice_Rec_2004425,Human_Splice_Rec_2004444,Human_Splice_Rec_2004445,Human_Splice_Rec_2004462 Human_miRNA_ID_2772848,Human_miRNA_ID_2772849 RMVar_hsa_circ_82356,RMVar_hsa_circ_86708,RMVar_hsa_circ_194688,RMVar_hsa_circ_121319,RMVar_hsa_circ_111339,RMVar_hsa_circ_118908,RMVar_hsa_circ_194689,RMVar_hsa_circ_194690,RMVar_hsa_circ_194691,RMVar_hsa_circ_311338,RMVar_hsa_circ_194692,RMVar_hsa_circ_194693 84268 RMVar_ID_84268 Human_SNP_ID_665387662 m1A Human chr19 + 38893527 38893527 38893527 GCGTCTGGGAGAATAAGTTCCGCAGGAAGTCCACTGACCGGAAAGAAGAGAGACAGCGGCAGGAC GCGTCTGGGAGAATAAGTTCCGCAGGAAGTCCGCTGACCGGAAAGAAGAGAGACAGCGGCAGGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38893511..38893595 26863196 MeRIP-seq:(Medium) rs1172707908 Functional Loss SNV dbSNP153 33..33 33 - - - 84269 RMVar_ID_84269 Human_SNP_ID_665388050 m1A Human chr19 - 38894846 38894846 38894846 GTATCATGAGTGACGAGGCAGAGGTCATTGGCATGGATGAGACAGGTAACCCCAGGAAAGTGGAA GTATCATGAGTGACGAGGCAGAGGTCATTGGCTTGGATGAGACAGGTAACCCCAGGAAAGTGGAA T A SIRT2 Ensembl:ENSG00000068903 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38894662..38895337 26863196 MeRIP-seq:(Medium) rs894980754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13451003 84270 RMVar_ID_84270 Human_SNP_ID_665389187 m1A Human chr19 - 38899561 38899560 38899561 GTGACGGGACACAGTGGTTGGTGACGGGACAGAGCGGTCGGTGACAGCCTCAAGGGCTTCAGCAC GTGACGGGACACAGTGGTTGGTGACGGGACAG_GCGGTCGGTGACAGCCTCAAGGGCTTCAGCAC CT C SIRT2 Ensembl:ENSG00000068903 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38899316..38899627 26863196 MeRIP-seq:(Medium) rs1368919513 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_521276,Human_RBP_ID_773329,Human_RBP_ID_4558419,Human_RBP_ID_18420927 Human_Splice_Rec_2004239,Human_Splice_Rec_2004295,Human_Splice_Rec_2004323,Human_Splice_Rec_2004385,Human_Splice_Rec_2004409,Human_Splice_Rec_2004429,Human_Splice_Rec_2004447,Human_Splice_Rec_2004473,Human_Splice_Rec_2004485,Human_Splice_Rec_2004495,Human_Splice_Rec_2004505,Human_Splice_Rec_2004515,Human_Splice_Rec_2004523,Human_Splice_Rec_2004531 84271 RMVar_ID_84271 Human_SNP_ID_665389381 m1A Human chr19 - 38900038 38900025 38900038 GCGTCGGCAGCTTTTCCCAAGCACGCGACCCCAGCCATGGCCCCCGCCGCCTCAGGGGCCCCCCG GCGTCGGCAGCTTTTCCCAAGCACGCGACCCC_____________GCCGCCTCAGGGGCCCCCCG CGGGGGCCATGGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38899995..38900130 26863196 MeRIP-seq:(Medium) rs1304569724 Functional Loss DEL dbSNP153 33..45 33 - - - 84272 RMVar_ID_84272 Human_SNP_ID_665390720 m1A Human chr19 - 38905277 38905277 38905277 CAGCGCCGTGTGGCCCCTACGCTCCGCCACACACAGCCCGGCGCCTGCTGCGTACAGCTTCTCCA CAGCGCCGTGTGGCCCCTACGCTCCGCCACACGCAGCCCGGCGCCTGCTGCGTACAGCTTCTCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:38905226..38907272 26863196 MeRIP-seq:(Medium) rs1209494671 Functional Loss SNV dbSNP153 33..33 33 - - - 84273 RMVar_ID_84273 Human_SNP_ID_665390804 m1A Human chr19 - 38905438 38905438 38905438 AAGTCGGAATCGGGGTACAAGGCGACAGGGGTATGGTTGGTGTCGGGAGTACGGTCAGGGCCCTG AAGTCGGAATCGGGGTACAAGGCGACAGGGGTGTGGTTGGTGTCGGGAGTACGGTCAGGGCCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38905388..38907272 26863196 MeRIP-seq:(Medium) rs374441253 Functional Loss SNV dbSNP153 33..33 33 - - - 84274 RMVar_ID_84274 Human_SNP_ID_665391572 m1A Human chr19 + 38907637 38907632 38907638 CGAGAAATCCGGCCCCTGCAGCAGCAGTAGCGACAGCGACAGCGGAGACGAGGGCGTGAGTCAGG CGAGAAATCCGGCCCCTGCAGCAGCAGT______AGCGACAGCGGAGACGAGGGCGTGAGTCAGG TAGCGAC T NFKBIB Ensembl:ENSG00000104825 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38907586..38908201 26863196 MeRIP-seq:(Medium) rs756150498 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_4526436 Human_Splice_Rec_2004549,Human_Splice_Rec_2004567 RMVar_hsa_circ_90770,RMVar_hsa_circ_194695 84275 RMVar_ID_84275 Human_SNP_ID_665391577 m1A Human chr19 + 38907637 38907637 38907637 CGAGAAATCCGGCCCCTGCAGCAGCAGTAGCGACAGCGACAGCGGAGACGAGGGCGTGAGTCAGG CGAGAAATCCGGCCCCTGCAGCAGCAGTAGCGTCAGCGACAGCGGAGACGAGGGCGTGAGTCAGG A T NFKBIB Ensembl:ENSG00000104825 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38907586..38908201 26863196 MeRIP-seq:(Medium) rs1324551653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4526436 Human_Splice_Rec_2004549,Human_Splice_Rec_2004567 RMVar_hsa_circ_90770,RMVar_hsa_circ_194695 84276 RMVar_ID_84276 Human_SNP_ID_665391907 m1A Human chr19 - 38908631 38908631 38908631 ATAGAGCACCCTAAGAATTAGGTCTCGCCTCAAAGCCCAAGTTCCCCTGCTCCTGGCTCAACCTC ATAGAGCACCCTAAGAATTAGGTCTCGCCTCAGAGCCCAAGTTCCCCTGCTCCTGGCTCAACCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38908595..38908844 32194978 MeRIP-seq:(Medium) rs1201705468 Functional Loss SNV dbSNP153 33..33 33 - - - 84277 RMVar_ID_84277 Human_SNP_ID_665392155 m1A Human chr19 - 38909318 38909315 38909318 ACTACCCCGTTTCTGACCCCACCAGGAAAAGGAGGTGGAGCAGCTGGAGCACTTGAGAGACGAAC ACTACCCCGTTTCTGACCCCACCAGGAAAAGG___TGGAGCAGCTGGAGCACTTGAGAGACGAAC ACCT A CCER2 Ensembl:ENSG00000262484 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:38909315..38911081 26863196 MeRIP-seq:(Medium) rs1313200630 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1294194 Human_Splice_Rec_2004584,Human_Splice_Rec_2004585,Human_Splice_Rec_2004594 RMVar_hsa_circ_194696 84278 RMVar_ID_84278 Human_SNP_ID_665392649 m1A Human chr19 + 38910821 38910821 38910821 CCATTCTCTAGATGCCGCTGCCACAGGTCCTCAAAGGTCTCCATGGGCCCCCTCTTCCTCTCCTC CCATTCTCTAGATGCCGCTGCCACAGGTCCTCCAAGGTCTCCATGGGCCCCCTCTTCCTCTCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:38909262..38910986 26863196 MeRIP-seq:(Medium) rs1400054910 Functional Loss SNV dbSNP153 33..33 33 - - - 84279 RMVar_ID_84279 Human_SNP_ID_665399962 m1A Human chr19 - 38932471 38932471 38932471 TGGGCTTCTTCGGCTTGCGGGTAAACGTGCACAGGACCACACCCTTCAGCTGCGGCCGGCCTTCC TGGGCTTCTTCGGCTTGCGGGTAAACGTGCACGGGACCACACCCTTCAGCTGCGGCCGGCCTTCC T C AC011455.2 Ensembl:ENSG00000269547 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38932324..38932548 26863196 MeRIP-seq:(Medium) rs1287203542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106956,RMVar_hsa_circ_194702 84280 RMVar_ID_84280 Human_SNP_ID_665402580 m1A Human chr19 + 38942739 38942739 38942739 TACGTAGCGGATGCCCTTGCCAAAGTTGGTGAAGACGTGGGAGACCTGCAGGGGGAAGGGGAGTG TACGTAGCGGATGCCCTTGCCAAAGTTGGTGAGGACGTGGGAGACCTGCAGGGGGAAGGGGAGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38942689..38944766 32194978 MeRIP-seq:(Medium) rs772597473 Functional Loss SNV dbSNP153 33..33 33 - - - 84281 RMVar_ID_84281 Human_SNP_ID_665403336 m1A Human chr19 + 38945337 38945325 38945338 GGTGGTCCTGGGGAGGAGCCAGAGCCTGGGGGAGGAGCCTGGGTGGTCCTGGGGTGGAGCCAGAG GGTGGTCCTGGGGAGGAGCCA_____________GAGCCTGGGTGGTCCTGGGGTGGAGCCAGAG AGAGCCTGGGGGAG A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:38945286..38945860 26863196 MeRIP-seq:(Medium) rs1413167100 Functional Loss DEL dbSNP153 22..34 33 - - - 84282 RMVar_ID_84282 Human_SNP_ID_665403339 m1A Human chr19 + 38945340 38945340 38945340 GGTCCTGGGGAGGAGCCAGAGCCTGGGGGAGGAGCCTGGGTGGTCCTGGGGTGGAGCCAGAGCCT GGTCCTGGGGAGGAGCCAGAGCCTGGGGGAGGGGCCTGGGTGGTCCTGGGGTGGAGCCAGAGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38945318..38945502 26863196 MeRIP-seq:(Medium) rs1231826466 Functional Loss SNV dbSNP153 33..33 33 - - - 84283 RMVar_ID_84283 Human_SNP_ID_665403448 m1A Human chr19 - 38945646 38945646 38945646 GCCCCTCCCCCAGGCTCTGGTTCCACCCCAGGACCACCCAGGCTCCTCCCCCAGGACCACCCAGG GCCCCTCCCCCAGGCTCTGGTTCCACCCCAGGGCCACCCAGGCTCCTCCCCCAGGACCACCCAGG T C AC011455.2,FBXO17 Ensembl:ENSG00000269547,Ensembl:ENSG00000269190 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38945625..38945763 26863196 MeRIP-seq:(Medium) rs1224639715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17081836 RMVar_hsa_circ_91641,RMVar_hsa_circ_194709 84284 RMVar_ID_84284 Human_SNP_ID_665403514 m1A Human chr19 - 38945857 38945857 38945857 CTACCTACCCAAAAGCCTCCAGAATCAACCGCAGGACCACCCAGGCTCCTCCCCCAGGACCACCC CTACCTACCCAAAAGCCTCCAGAATCAACCGCCGGACCACCCAGGCTCCTCCCCCAGGACCACCC T G AC011455.2,FBXO17 Ensembl:ENSG00000269547,Ensembl:ENSG00000269190 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38945855..38946055 32194978 MeRIP-seq:(Medium) rs1441887173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17083956 RMVar_hsa_circ_91641,RMVar_hsa_circ_194709 84285 RMVar_ID_84285 Human_SNP_ID_665411089 m1A Human chr19 + 38975684 38975684 38975684 AGTCGAGGGGCTCCCCGTGATCGGCGTGGCCCAGGGGGCCCCGGGACCGGCGGTCTGGGCGGTCG AGTCGAGGGGCTCCCCGTGATCGGCGTGGCCCGGGGGGCCCCGGGACCGGCGGTCTGGGCGGTCG A G AC011455.6 Ensembl:ENSG00000287271 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38975589..38975717 26863196 MeRIP-seq:(Medium) rs1264854852 Functional Loss SNV dbSNP153 33..33 33 - - - 84286 RMVar_ID_84286 Human_SNP_ID_665425571 m1A Human chr19 - 39031107 39031107 39031107 CTCCTGCATTCCCAGCTGGTGTTGCAAGAAGCAGGTCTTGGACCTAGAGGAGGAGGGTCTGTGGC CTCCTGCATTCCCAGCTGGTGTTGCAAGAAGCGGGTCTTGGACCTAGAGGAGGAGGGTCTGTGGC T C FBXO27 Ensembl:ENSG00000161243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39026968..39031141 26863196 MeRIP-seq:(Medium) rs756786324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4568044 Human_Splice_Rec_2004886,Human_Splice_Rec_2004887,Human_Splice_Rec_2004896,Human_Splice_Rec_2004897,Human_Splice_Rec_2004906,Human_Splice_Rec_2004907,Human_Splice_Rec_2004913,Human_Splice_Rec_2004918,Human_Splice_Rec_2004919 RMVar_hsa_circ_84056,RMVar_hsa_circ_94461,RMVar_hsa_circ_87169,RMVar_hsa_circ_194711,RMVar_hsa_circ_194712,RMVar_hsa_circ_97164,RMVar_hsa_circ_77676,RMVar_hsa_circ_194713,RMVar_hsa_circ_194715,RMVar_hsa_circ_194714 84287 RMVar_ID_84287 Human_SNP_ID_665425572 m1A Human chr19 - 39031107 39031107 39031107 CTCCTGCATTCCCAGCTGGTGTTGCAAGAAGCAGGTCTTGGACCTAGAGGAGGAGGGTCTGTGGC CTCCTGCATTCCCAGCTGGTGTTGCAAGAAGCCGGTCTTGGACCTAGAGGAGGAGGGTCTGTGGC T G FBXO27 Ensembl:ENSG00000161243 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39026968..39031141 26863196 MeRIP-seq:(Medium) rs756786324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4568044 Human_Splice_Rec_2004886,Human_Splice_Rec_2004887,Human_Splice_Rec_2004896,Human_Splice_Rec_2004897,Human_Splice_Rec_2004906,Human_Splice_Rec_2004907,Human_Splice_Rec_2004913,Human_Splice_Rec_2004918,Human_Splice_Rec_2004919 RMVar_hsa_circ_84056,RMVar_hsa_circ_94461,RMVar_hsa_circ_87169,RMVar_hsa_circ_194711,RMVar_hsa_circ_194712,RMVar_hsa_circ_97164,RMVar_hsa_circ_77676,RMVar_hsa_circ_194713,RMVar_hsa_circ_194715,RMVar_hsa_circ_194714 84288 RMVar_ID_84288 Human_SNP_ID_665425659 m1A Human chr19 + 39031289 39031289 39031289 GTCCTGTTTTCCTCCACCACCCAGCCGTCCCCACCGTGTTGCACCATCCACTTTCGGAGGCCTTC GTCCTGTTTTCCTCCACCACCCAGCCGTCCCCCCCGTGTTGCACCATCCACTTTCGGAGGCCTTC A C AC010605.1 Ensembl:ENSG00000267992 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39031240..39031340 26863196 MeRIP-seq:(Medium) rs758880405 Functional Loss SNV dbSNP153 33..33 33 - - - 84289 RMVar_ID_84289 Human_SNP_ID_665425660 m1A Human chr19 + 39031289 39031289 39031289 GTCCTGTTTTCCTCCACCACCCAGCCGTCCCCACCGTGTTGCACCATCCACTTTCGGAGGCCTTC GTCCTGTTTTCCTCCACCACCCAGCCGTCCCCGCCGTGTTGCACCATCCACTTTCGGAGGCCTTC A G AC010605.1 Ensembl:ENSG00000267992 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39031240..39031340 26863196 MeRIP-seq:(Medium) rs758880405 Functional Loss SNV dbSNP153 33..33 33 - - - 84290 RMVar_ID_84290 Human_SNP_ID_665451528 m1A Human chr19 - 39125881 39125881 39125881 GGCGCCGCAGTCGCTCGCGGCCTAACTGCTCGACCTGGAACTCCGCGCCCTCGCGCCTCCCTCAG GGCGCCGCAGTCGCTCGCGGCCTAACTGCTCGGCCTGGAACTCCGCGCCCTCGCGCCTCCCTCAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:39125801..39125943 26863410 MeRIP-seq:(Medium) rs4803206 Functional Loss SNV dbSNP153 33..33 33 - - - 84291 RMVar_ID_84291 Human_SNP_ID_665453000 m1A Human chr19 - 39130328 39130328 39130328 CCAATCCCTCTCTGTGCCCCTCCCCACCATCCAGCCCCAACCCCTCTGCCTGGGTTTCCCCATCC CCAATCCCTCTCTGTGCCCCTCCCCACCATCCCGCCCCAACCCCTCTGCCTGGGTTTCCCCATCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:39130322..39130451 26863196 MeRIP-seq:(Medium) rs12980781 Functional Loss SNV dbSNP153 33..33 33 - - - 84292 RMVar_ID_84292 Human_SNP_ID_665464327 m1A Human chr19 - 39169648 39169648 39169648 TCAGGCTCTGCCACTGGCGGGGCAGCCCCGTGAACTTCTGCTCGTGCTGGTCGAAGCCCGTGTGC TCAGGCTCTGCCACTGGCGGGGCAGCCCCGTGGACTTCTGCTCGTGCTGGTCGAAGCCCGTGTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39169597..39169697 32194978 MeRIP-seq:(Medium) rs1369491877 Functional Loss SNV dbSNP153 33..33 33 - - - 84293 RMVar_ID_84293 Human_SNP_ID_665465701 m1A Human chr19 - 39173609 39173609 39173609 GGAGGACTGGGGGATGGCCAGGCCCCCCGCTGATGGCCCGTTAGGGGCCACGTCATGAGGCTCCC GGAGGACTGGGGGATGGCCAGGCCCCCCGCTGGTGGCCCGTTAGGGGCCACGTCATGAGGCTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39173599..39173802 26863196 MeRIP-seq:(Medium) rs757380530 Functional Loss SNV dbSNP153 33..33 33 - - - 84294 RMVar_ID_84294 Human_SNP_ID_665466850 m1A Human chr19 + 39176714 39176714 39176714 AGAGCTCATCTCCCGCCTTCCCTACGGGCCAGAGGTGAGCCCCGGGGTGGCTTGGTTGTCCCGCC AGAGCTCATCTCCCGCCTTCCCTACGGGCCAGGGGTGAGCCCCGGGGTGGCTTGGTTGTCCCGCC A G PAK4 Ensembl:ENSG00000130669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39176665..39177725 26863196 MeRIP-seq:(Medium) rs775346914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1015796 Human_Splice_Rec_2005019,Human_Splice_Rec_2005035,Human_Splice_Rec_2005059,Human_Splice_Rec_2005081,Human_Splice_Rec_2005097,Human_Splice_Rec_2005119,Human_Splice_Rec_2005125,Human_Splice_Rec_2005129 RMVar_hsa_circ_269730 84295 RMVar_ID_84295 Human_SNP_ID_665467188 m1A Human chr19 - 39177770 39177770 39177770 AGGTTCTTCAGTCGGGGTGGCAGGTTGTCCCGAATCATCTTCATGGCTTTGAGGGGTGGCTCGTT AGGTTCTTCAGTCGGGGTGGCAGGTTGTCCCGGATCATCTTCATGGCTTTGAGGGGTGGCTCGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39177721..39177832 26863196 MeRIP-seq:(Medium) rs1203252048 Functional Loss SNV dbSNP153 33..33 33 - - - 84296 RMVar_ID_84296 Human_SNP_ID_665467694 m1A Human chr19 + 39179139 39179139 39179139 TGCGCCCCCTTTCTGTGGCTGGATGGGGAGACAGGTCAGGGCCCCCCACCCTCTCCAGCCCCTGC TGCGCCCCCTTTCTGTGGCTGGATGGGGAGACCGGTCAGGGCCCCCCACCCTCTCCAGCCCCTGC A C PAK4 Ensembl:ENSG00000130669 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39179089..39179237 26863196 MeRIP-seq:(Medium) rs559205146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521388,Human_RBP_ID_5145205,Human_RBP_ID_5650975,Human_RBP_ID_6760857,Human_RBP_ID_17656117,Human_RBP_ID_17924312,Human_RBP_ID_23796745,Human_RBP_ID_26472486,Human_RBP_ID_27273945 Human_miRNA_ID_730382 84297 RMVar_ID_84297 Human_SNP_ID_665472745 m1A Human chr19 + 39197032 39197032 39197032 GGGACACGCGCTCGGTGGCGGGATGGAAGCCGATGGGCCCGCGAGCCTCCAGGAGCTGCCTCCCT GGGACACGCGCTCGGTGGCGGGATGGAAGCCGGTGGGCCCGCGAGCCTCCAGGAGCTGCCTCCCT A G NCCRP1 Ensembl:ENSG00000188505 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39196985..39197221 26863196 MeRIP-seq:(Medium) rs1324632700 Functional Loss SNV dbSNP153 33..33 33 - - - 84298 RMVar_ID_84298 Human_SNP_ID_665472769 m1A Human chr19 - 39197109 39197082 39197109 CGGGGCTGCGGGCGATGGCAGCGACGGCGGCGAGGGCAGTGGTGGCGGCGACGGCGGCGGTGAAG CGGGGCTGCGGGCGATGGCAGCGACGGCGGCG___________________________GTGAAG CCGCCGCCGTCGCCGCCACCACTGCCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39196984..39197136 26863196 MeRIP-seq:(Medium) rs968189354 Functional Loss DEL dbSNP153 33..59 33 - - - 84299 RMVar_ID_84299 Human_SNP_ID_665502340 m1A Human chr19 + 39307045 39307045 39307045 CCGAGGGACAAGAGACGACAGGACAGAGAGAAAGGAGAGGCAAATAGGGAAAGACAGGCACTACA CCGAGGGACAAGAGACGACAGGACAGAGAGAAGGGAGAGGCAAATAGGGAAAGACAGGCACTACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39306995..39307129 26863196 MeRIP-seq:(Medium) rs1052560002 Functional Loss SNV dbSNP153 33..33 33 - - - 84300 RMVar_ID_84300 Human_SNP_ID_665504277 m1A Human chr19 - 39314270 39314270 39314270 CCGGACCCGGGTCCGGGGGGACGGGACGCTGGATGTGACCATCACCACCTTGAGGGACAGTGGCA CCGGACCCGGGTCCGGGGGGACGGGACGCTGGGTGTGACCATCACCACCTTGAGGGACAGTGGCA T C LRFN1 Ensembl:ENSG00000128011 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39314268..39314415 26863196 MeRIP-seq:(Medium) rs775608969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1294252,Human_RBP_ID_8833772 Human_miRNA_ID_2697965 RMVar_hsa_circ_117745,RMVar_hsa_circ_194718 84301 RMVar_ID_84301 Human_SNP_ID_665504728 m1A Human chr19 + 39315320 39315320 39315320 CAGCGGGCGGCGGCGAGAGGAGGGCCGAGGAGAAGGGTCCTGGAGCCATGGTGCAGTGGGAAGGC CAGCGGGCGGCGGCGAGAGGAGGGCCGAGGAGGAGGGTCCTGGAGCCATGGTGCAGTGGGAAGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:39315224..39315390 26863196 MeRIP-seq:(Medium) rs1253871543 Functional Loss SNV dbSNP153 33..33 33 - - - 84302 RMVar_ID_84302 Human_SNP_ID_665506030 m1A Human chr19 - 39320831 39320831 39320831 GGCCCTCCCCCCACCATGGCGCGGAGCGAGGCAGCGGCGGCGGGGCCGGGCCCGGGGCCCCCCCG GGCCCTCCCCCCACCATGGCGCGGAGCGAGGCGGCGGCGGCGGGGCCGGGCCCGGGGCCCCCCCG T C AC011445.1 Ensembl:ENSG00000268262 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39320748..39320856 26863196 MeRIP-seq:(Medium) rs866839667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2005217 RMVar_hsa_circ_114797,RMVar_hsa_circ_194719 84303 RMVar_ID_84303 Human_SNP_ID_665511702 m1A Human chr19 + 39342516 39342516 39342516 GGGAGGGGAGCTTGCGGGCCCGAGAGGGGGCGACGGCGGCGGCGGTGGCCTGAGGAGGCCCGAGC GGGAGGGGAGCTTGCGGGCCCGAGAGGGGGCGGCGGCGGCGGCGGTGGCCTGAGGAGGCCCGAGC A G SAMD4B Ensembl:ENSG00000179134 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:39342470..39342632 26863196 MeRIP-seq:(Medium) rs1197446300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241871,Human_RBP_ID_3954988,Human_RBP_ID_4557480,Human_RBP_ID_5130405,Human_RBP_ID_5320362,Human_RBP_ID_8196480,Human_RBP_ID_8840029,Human_RBP_ID_9328930,Human_RBP_ID_9425324,Human_RBP_ID_18420929,Human_RBP_ID_18461939,Human_RBP_ID_18997742,Human_RBP_ID_22070179,Human_RBP_ID_23796954,Human_RBP_ID_24552843,Human_RBP_ID_26783766,Human_RBP_ID_27839546 Human_Splice_Rec_2005331,Human_Splice_Rec_2005337,Human_Splice_Rec_2005361 84304 RMVar_ID_84304 Human_SNP_ID_665515247 m1A Human chr19 - 39356657 39356657 39356657 CCTGAAAAAGGAAGCAAAGGGGTCAAACAGAAAGAAGGGGCTGAAACTTGCCTGGTGAGTGTGGG CCTGAAAAAGGAAGCAAAGGGGTCAAACAGAAGGAAGGGGCTGAAACTTGCCTGGTGAGTGTGGG T C lnc-LRFN1-2 RNACentral:URS00008BA9A0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39356653..39356800 26863196 MeRIP-seq:(Medium) rs1289341027 Functional Loss SNV dbSNP153 33..33 33 - - - 84305 RMVar_ID_84305 Human_SNP_ID_665515293 m1A Human chr19 - 39356798 39356798 39356798 CCCGGCTCTGGCCTCCTGTTACCTTTCCCCTGAGGGCCAGGGCTTAAGGACGTTTCTGGGCGTGG CCCGGCTCTGGCCTCCTGTTACCTTTCCCCTGCGGGCCAGGGCTTAAGGACGTTTCTGGGCGTGG T G lnc-LRFN1-2 RNACentral:URS00008BA9A0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:39356751..39356925 26863196 MeRIP-seq:(Medium) rs531735341 Functional Loss SNV dbSNP153 33..33 33 - - - 84306 RMVar_ID_84306 Human_SNP_ID_665515336 m1A Human chr19 + 39356891 39356891 39356891 CGCCGTCCCCCGACCCTGGCCCCAGGCCCGGCACCATGATGTTCCGAGACCAGGTGGGCATCCTC CGCCGTCCCCCGACCCTGGCCCCAGGCCCGGCCCCATGATGTTCCGAGACCAGGTGGGCATCCTC A C SAMD4B Ensembl:ENSG00000179134 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:39356676..39356925 26863196 MeRIP-seq:(Medium) rs1172094087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559592,Human_RBP_ID_22591871 RMVar_hsa_circ_2889,RMVar_hsa_circ_282463,RMVar_hsa_circ_333351,RMVar_hsa_circ_339646,RMVar_hsa_circ_310231,RMVar_hsa_circ_49018,RMVar_hsa_circ_93073,RMVar_hsa_circ_22957,RMVar_hsa_circ_23402,RMVar_hsa_circ_338453,RMVar_hsa_circ_194721,RMVar_hsa_circ_65374 84307 RMVar_ID_84307 Human_SNP_ID_665515361 m1A Human chr19 - 39356991 39356991 39356991 AGAGCTGCAGGAAGCGGGCCTGGGTACGGGTGACCCGTTTCAGAAGTGACAGGAGGGCCACTGTC AGAGCTGCAGGAAGCGGGCCTGGGTACGGGTGGCCCGTTTCAGAAGTGACAGGAGGGCCACTGTC T C lnc-LRFN1-2 RNACentral:URS00008BA9A0 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39356878..39357029 32194978 MeRIP-seq:(Medium) rs760368661 Functional Loss SNV dbSNP153 33..33 33 - - - 84308 RMVar_ID_84308 Human_SNP_ID_665518573 m1A Human chr19 + 39370077 39370077 39370077 GGGAAAATGGACACGTGCCCTTCCACCCATCCAGCTCAGTGCCGCCAGCCATCAACAGTATTGGG GGGAAAATGGACACGTGCCCTTCCACCCATCCGGCTCAGTGCCGCCAGCCATCAACAGTATTGGG A G SAMD4B Ensembl:ENSG00000179134 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:39370026..39370148;chr19:39370026..39370160 26863196 MeRIP-seq:(Medium) rs777616036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6761376,Human_RBP_ID_17269009,Human_RBP_ID_17924442,Human_RBP_ID_18192242,Human_RBP_ID_27274076 Human_Splice_Rec_2005341,Human_Splice_Rec_2005371,Human_Splice_Rec_2005397,Human_Splice_Rec_2005419,Human_Splice_Rec_2005443,Human_Splice_Rec_2005447,Human_Splice_Rec_2005449 Human_miRNA_ID_2000829 RMVar_hsa_circ_2889,RMVar_hsa_circ_333351,RMVar_hsa_circ_310231,RMVar_hsa_circ_49018,RMVar_hsa_circ_93073,RMVar_hsa_circ_22957,RMVar_hsa_circ_40388,RMVar_hsa_circ_338453,RMVar_hsa_circ_194721,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_194722 84309 RMVar_ID_84309 Human_SNP_ID_665519382 m1A Human chr19 + 39373514 39373514 39373514 GAGGGAGGCTAGTGAGGAGGGCAGCAAGCGCCAGGCCTGAGGCAGCAGCAGAGGGGTACATGACC GAGGGAGGCTAGTGAGGAGGGCAGCAAGCGCCGGGCCTGAGGCAGCAGCAGAGGGGTACATGACC A G SAMD4B Ensembl:ENSG00000179134 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39373513..39373628 26863196 MeRIP-seq:(Medium) rs976850072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6761409 RMVar_hsa_circ_2889,RMVar_hsa_circ_333351,RMVar_hsa_circ_49018,RMVar_hsa_circ_93073,RMVar_hsa_circ_22957,RMVar_hsa_circ_40388,RMVar_hsa_circ_194721,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_194722 84310 RMVar_ID_84310 Human_SNP_ID_665519886 m1A Human chr19 + 39375706 39375706 39375706 GCCCACTGAAGCGCTCCATGTCACTCATCCCTACAAGCCCCCAGGTCCCTGGTGAGTGGCCGAGT GCCCACTGAAGCGCTCCATGTCACTCATCCCTGCAAGCCCCCAGGTCCCTGGTGAGTGGCCGAGT A G SAMD4B Ensembl:ENSG00000179134 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39375629..39375803 26863196 MeRIP-seq:(Medium) rs772296491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1015892,Human_RBP_ID_9293675,Human_RBP_ID_9328932,Human_RBP_ID_17269012,Human_RBP_ID_17384061,Human_RBP_ID_17924447 Human_Splice_Rec_2005342,Human_Splice_Rec_2005372,Human_Splice_Rec_2005398,Human_Splice_Rec_2005420,Human_Splice_Rec_2005444,Human_Splice_Rec_2005448 RMVar_hsa_circ_2889,RMVar_hsa_circ_333351,RMVar_hsa_circ_49018,RMVar_hsa_circ_93073,RMVar_hsa_circ_22957,RMVar_hsa_circ_40388,RMVar_hsa_circ_194721,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_194723,RMVar_hsa_circ_194722,RMVar_hsa_circ_347309 84311 RMVar_ID_84311 Human_SNP_ID_665520420 m1A Human chr19 + 39377716 39377716 39377716 GCACCGAGGCCAAGGACCCTCCAGCTGTGGAGAACTACCCACCTCCACCAGCTCCAGCTCCCACT GCACCGAGGCCAAGGACCCTCCAGCTGTGGAGGACTACCCACCTCCACCAGCTCCAGCTCCCACT A G SAMD4B Ensembl:ENSG00000179134 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:39377701..39377725 26863196 MeRIP-seq:(Medium) rs1203895786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521577,Human_RBP_ID_8487126,Human_RBP_ID_17269017,Human_RBP_ID_17384064,Human_RBP_ID_17499946,Human_RBP_ID_18732296,Human_RBP_ID_27468002 Human_miRNA_ID_2052764 RMVar_hsa_circ_2889,RMVar_hsa_circ_333351,RMVar_hsa_circ_49018,RMVar_hsa_circ_39316,RMVar_hsa_circ_40388,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_126420,RMVar_hsa_circ_194723,RMVar_hsa_circ_194722,RMVar_hsa_circ_347309,RMVar_hsa_circ_127033,RMVar_hsa_circ_194726,RMVar_hsa_circ_124151,RMVar_hsa_circ_194727,RMVar_hsa_circ_194725 84312 RMVar_ID_84312 Human_SNP_ID_665521338 m1A Human chr19 + 39381026 39381026 39381026 TGTGGTTTGCCAACCCTGGAGGCAGCAACAGCATGCCCAGTCAGAGCCGCAGCTCTGTGCAGCGC TGTGGTTTGCCAACCCTGGAGGCAGCAACAGCCTGCCCAGTCAGAGCCGCAGCTCTGTGCAGCGC A C SAMD4B Ensembl:ENSG00000179134 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39380715..39381168 32194978 MeRIP-seq:(Medium) rs1206542309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521587,Human_RBP_ID_18732300 Human_Splice_Rec_2005356,Human_Splice_Rec_2005357,Human_Splice_Rec_2005386,Human_Splice_Rec_2005387,Human_Splice_Rec_2005412,Human_Splice_Rec_2005413,Human_Splice_Rec_2005434,Human_Splice_Rec_2005435,Human_Splice_Rec_2005456,Human_Splice_Rec_2005458,Human_Splice_Rec_2005459 Human_miRNA_ID_3070150 RMVar_hsa_circ_49018,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_194722,RMVar_hsa_circ_124151,RMVar_hsa_circ_194725,RMVar_hsa_circ_89518,RMVar_hsa_circ_194729 84313 RMVar_ID_84313 Human_SNP_ID_665521986 m1A Human chr19 - 39383558 39383558 39383558 GTTGGGGGTTGGCCCCCGCCCGCCGCCCAGGGAGCCTATGGGTGCGCTGGGCTGTGGGTCCCGTC GTTGGGGGTTGGCCCCCGCCCGCCGCCCAGGGGGCCTATGGGTGCGCTGGGCTGTGGGTCCCGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39383526..39383875 32194978 MeRIP-seq:(Medium) rs750887873 Functional Loss SNV dbSNP153 33..33 33 - - - 84314 RMVar_ID_84314 Human_SNP_ID_665522094 m1A Human chr19 - 39383839 39383836 39383839 TGGGGAGAGGCAGGTGGTCAGCGGTCTGGAGGAGGCAGGGGTGGGATGGGACCAGGTGGGGATGA TGGGGAGAGGCAGGTGGTCAGCGGTCTGGAGG___CAGGGGTGGGATGGGACCAGGTGGGGATGA GCCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39383788..39383951 26863196 MeRIP-seq:(Medium) rs1436867107 Functional Loss DEL dbSNP153 33..35 33 - - - 84315 RMVar_ID_84315 Human_SNP_ID_665522096 m1A Human chr19 - 39383839 39383839 39383839 TGGGGAGAGGCAGGTGGTCAGCGGTCTGGAGGAGGCAGGGGTGGGATGGGACCAGGTGGGGATGA TGGGGAGAGGCAGGTGGTCAGCGGTCTGGAGGCGGCAGGGGTGGGATGGGACCAGGTGGGGATGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39383788..39383951 26863196 MeRIP-seq:(Medium) rs1409811251 Functional Loss SNV dbSNP153 33..33 33 - - - 84316 RMVar_ID_84316 Human_SNP_ID_665522705 m1A Human chr19 - 39386001 39386001 39386001 TGCAGCTTCTGATTCCAGTGAAGCTGATAGTGACAGTGACTGAGTCCCAGGGCATTCAGGGCTGG TGCAGCTTCTGATTCCAGTGAAGCTGATAGTGCCAGTGACTGAGTCCCAGGGCATTCAGGGCTGG T G PAF1 Ensembl:ENSG00000006712 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39385950..39387221 32194978 MeRIP-seq:(Medium) rs1386771175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521667,Human_RBP_ID_1564806,Human_RBP_ID_1887428,Human_RBP_ID_3571610,Human_RBP_ID_6761526,Human_RBP_ID_8487157,Human_RBP_ID_8833887,Human_RBP_ID_18732330 Human_miRNA_ID_3091293 RMVar_hsa_circ_96937,RMVar_hsa_circ_194731,RMVar_hsa_circ_93122,RMVar_hsa_circ_194730 84317 RMVar_ID_84317 Human_SNP_ID_665522839 m1A Human chr19 + 39386354 39386354 39386354 TCCTCCCGTTCACTCTCGCTGCCCGAGTGCTCATCTTCACTGCCCTCCTTCTCACTGCTGCTGCC TCCTCCCGTTCACTCTCGCTGCCCGAGTGCTCGTCTTCACTGCCCTCCTTCTCACTGCTGCTGCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr19:39386201..39386575;chr19:39386253..39386500 26863196 MeRIP-seq:(Medium) rs769715236 Functional Loss SNV dbSNP153 33..33 33 - - - 84318 RMVar_ID_84318 Human_SNP_ID_665524235 m1A Human chr19 + 39390939 39390911 39390939 CGAAGGGGGACGCAGAGGGGCGTGCCGACTTCAGGGGACGCCTGATCCGAGGAAGGCCCAGCTTG CGAAG____________________________GGGGACGCCTGATCCGAGGAAGGCCCAGCTTG GGGGGACGCAGAGGGGCGTGCCGACTTCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39390890..39391096 26863196 MeRIP-seq:(Medium) rs1164640876 Functional Loss DEL dbSNP153 6..33 33 - - - 84319 RMVar_ID_84319 Human_SNP_ID_665524578 m1A Human chr19 + 39391577 39391577 39391577 TGCCCAGAGCGGCCTCCTGCAGCAACAGCAACAGGACTTCGATCCTGTGCAGCGTTATAAGATGC TGCCCAGAGCGGCCTCCTGCAGCAACAGCAACCGGACTTCGATCCTGTGCAGCGTTATAAGATGC A C MED29 Ensembl:ENSG00000063322 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39391526..39391600 32194978 MeRIP-seq:(Medium) rs1356688952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4527523 Human_Splice_Rec_2005553,Human_Splice_Rec_2005557,Human_Splice_Rec_2005563,Human_Splice_Rec_2005569,Human_Splice_Rec_2005575,Human_Splice_Rec_2005581 84320 RMVar_ID_84320 Human_SNP_ID_665526058 m1A Human chr19 - 39396019 39396019 39396019 ACTCAGTTTCCACCTCTGCACTAATGGCGCCCACACTGTCGCTGGCCTCCCCCTGACATTTGTAG ACTCAGTTTCCACCTCTGCACTAATGGCGCCCGCACTGTCGCTGGCCTCCCCCTGACATTTGTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39396015..39396105 26863196 MeRIP-seq:(Medium) rs747136903 Functional Loss SNV dbSNP153 33..33 33 - - - 84321 RMVar_ID_84321 Human_SNP_ID_665527199 m1A Human chr19 - 39400196 39400196 39400196 TTTTGAATTTTTTGCAGATAAGGGCTTTTGCTATGTTGCTCGGACTGGTCTTGAATTCCTGGGCT TTTTGAATTTTTTGCAGATAAGGGCTTTTGCTGTGTTGCTCGGACTGGTCTTGAATTCCTGGGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39400147..39400254 26863196 MeRIP-seq:(Medium) rs112947797 Functional Loss SNV dbSNP153 33..33 33 - - - 84322 RMVar_ID_84322 Human_SNP_ID_665529028 m1A Human chr19 - 39406869 39406869 39406869 GTAACGGTTGGCCATGAGGGGTGTCGGCCGAGAGTGGGAGCGCTGAAGTCAGGCTGAGGCTGGCA GTAACGGTTGGCCATGAGGGGTGTCGGCCGAGGGTGGGAGCGCTGAAGTCAGGCTGAGGCTGGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:39406851..39407100 26863196 MeRIP-seq:(Medium) rs777494175 Functional Loss SNV dbSNP153 33..33 33 - - - 84323 RMVar_ID_84323 Human_SNP_ID_665529056 m1A Human chr19 - 39406906 39406906 39406906 GGGGACTCACCTCGTAGATGGCAGTCAGATCCATGGTGTAACGGTTGGCCATGAGGGGTGTCGGC GGGGACTCACCTCGTAGATGGCAGTCAGATCCGTGGTGTAACGGTTGGCCATGAGGGGTGTCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39406901..39406998 26863196 MeRIP-seq:(Medium) rs1253840217 Functional Loss SNV dbSNP153 33..33 33 - - - 84324 RMVar_ID_84324 Human_SNP_ID_665529062 m1A Human chr19 + 39406924 39406924 39406924 CAACCGTTACACCATGGATCTGACTGCCATCTACGAGGTGAGTCCCCGCCGCACGGCATCCCCGG CAACCGTTACACCATGGATCTGACTGCCATCTGCGAGGTGAGTCCCCGCCGCACGGCATCCCCGG A G ZFP36 Ensembl:ENSG00000128016 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39406875..39407065 26863196 MeRIP-seq:(Medium) rs1381523453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090123 Human_Splice_Rec_2005587,Human_Splice_Rec_2005589,Human_Splice_Rec_2005593 84325 RMVar_ID_84325 Human_SNP_ID_665529383 m1A Human chr19 - 39407872 39407872 39407872 CACTAGGCTGGTGGAGCGGCCAGGCAGGCGGGAGGTGACCCCAGACGGGCTGGAGTCGGAGGGGC CACTAGGCTGGTGGAGCGGCCAGGCAGGCGGGGGGTGACCCCAGACGGGCTGGAGTCGGAGGGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:39407860..39407987 26863196 MeRIP-seq:(Medium) rs1466516327 Functional Loss SNV dbSNP153 33..33 33 - - - 84326 RMVar_ID_84326 Human_SNP_ID_665529428 m1A Human chr19 - 39407958 39407958 39407958 GGTGAGGGTGACAGCTCAGGGCCCAGGCGGGGAGCCAGCGGTGCGAAGCCAGGGGGTGGGGGCAC GGTGAGGGTGACAGCTCAGGGCCCAGGCGGGGCGCCAGCGGTGCGAAGCCAGGGGGTGGGGGCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39407907..39408036 26863196 MeRIP-seq:(Medium) rs759746703 Functional Loss SNV dbSNP153 33..33 33 - - - 84327 RMVar_ID_84327 Human_SNP_ID_665530649 m1A Human chr19 - 39412183 39412183 39412183 GCGAGCGGAGCAATGCCGAGGTTGTGAGTTCGATCCTCACCTGGAGCACTTTTTTTCCCCATCAG GCGAGCGGAGCAATGCCGAGGTTGTGAGTTCGGTCCTCACCTGGAGCACTTTTTTTCCCCATCAG T C tRNA-Ile-TAT-1-1,TRI-TAT1-1,lnc-RPS16-3 RNACentral:URS0000757938,RNACentral:URS00006CAA11,RNACentral:URS0000D573E3 tRNA,tRNA,lincRNA exon,intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs921395547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521692,Human_RBP_ID_1189749,Human_RBP_ID_1294291,Human_RBP_ID_1373310,Human_RBP_ID_1564850,Human_RBP_ID_1887472,Human_RBP_ID_3571646,Human_RBP_ID_4568383,Human_RBP_ID_5261529,Human_RBP_ID_5275314,Human_RBP_ID_5468783,Human_RBP_ID_6761670,Human_RBP_ID_8256109,Human_RBP_ID_8487212,Human_RBP_ID_8833910,Human_RBP_ID_9087856,Human_RBP_ID_13453597,Human_RBP_ID_17010466,Human_RBP_ID_17388328,Human_RBP_ID_17695683,Human_RBP_ID_17924560,Human_RBP_ID_18200640,Human_RBP_ID_18208552,Human_RBP_ID_18441334,Human_RBP_ID_18732371,Human_RBP_ID_20390636,Human_RBP_ID_22005476,Human_RBP_ID_22234867,Human_RBP_ID_22810795,Human_RBP_ID_23131249,Human_RBP_ID_23797057,Human_RBP_ID_24420237,Human_RBP_ID_24485353,Human_RBP_ID_26653716,Human_RBP_ID_27679795 84328 RMVar_ID_84328 Human_SNP_ID_665530941 m1A Human chr19 - 39412660 39412660 39412660 TGTGACGGCGGCGGCGCCACATCTGGGGCGGGAGAGTCCGATCCCAGCTGTGAGGCGGGGGGCGG TGTGACGGCGGCGGCGCCACATCTGGGGCGGGGGAGTCCGATCCCAGCTGTGAGGCGGGGGGCGG T C lnc-RPS16-3 RNACentral:URS0000D573E3 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39412610..39412780 26863196 MeRIP-seq:(Medium) rs1434760709 Functional Loss SNV dbSNP153 33..33 33 - - - 84329 RMVar_ID_84329 Human_SNP_ID_665532683 m1A Human chr19 - 39417949 39417949 39417949 AACGCGCCCTCCAACACCAGTTCCCCAAAAGCACTGAGCTCTGGTCCGGTCCAGCCACCCAGCCG AACGCGCCCTCCAACACCAGTTCCCCAAAAGCGCTGAGCTCTGGTCCGGTCCAGCCACCCAGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39417818..39418039 26863196 MeRIP-seq:(Medium) rs1354112675 Functional Loss SNV dbSNP153 33..33 33 - - - 84330 RMVar_ID_84330 Human_SNP_ID_665538525 m1A Human chr19 - 39435517 39435517 39435517 TGTAGCTCTTGAAAGCTGGGGGGGCTGGCATCAGCAACGGGATGTTTAGAAGTTGTGTTGGGTGT TGTAGCTCTTGAAAGCTGGGGGGGCTGGCATCGGCAACGGGATGTTTAGAAGTTGTGTTGGGTGT T C RPS16 Ensembl:ENSG00000105193 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:39435514..39435882 26863196 MeRIP-seq:(Medium) rs1430030173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5373883,Human_RBP_ID_6761778,Human_RBP_ID_13453748,Human_RBP_ID_22502835,Human_RBP_ID_22810818,Human_RBP_ID_25415927,Human_RBP_ID_27679810 RMVar_hsa_circ_79650,RMVar_hsa_circ_88795,RMVar_hsa_circ_194750,RMVar_hsa_circ_194749,RMVar_hsa_circ_34356 84331 RMVar_ID_84331 Human_SNP_ID_665538598 m1A Human chr19 - 39435663 39435663 39435663 CTGTGGCGCACTGCAAACGCGGCAATGGTCTCATCAAGGTGAACGGGCGGCCCCTGGAGATGATT CTGTGGCGCACTGCAAACGCGGCAATGGTCTCCTCAAGGTGAACGGGCGGCCCCTGGAGATGATT T G RPS16 Ensembl:ENSG00000105193 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:39435522..39435868 26863196 MeRIP-seq:(Medium) rs772779579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521735,Human_RBP_ID_1189765,Human_RBP_ID_1564921,Human_RBP_ID_1887504,Human_RBP_ID_4527771,Human_RBP_ID_9087872,Human_RBP_ID_9330029,Human_RBP_ID_17656132,Human_RBP_ID_17934983,Human_RBP_ID_18192254,Human_RBP_ID_18732441,Human_RBP_ID_22447749,Human_RBP_ID_26468202,Human_RBP_ID_26817547,Human_RBP_ID_26989858,Human_RBP_ID_27274190 Human_Splice_Rec_2005788,Human_Splice_Rec_2005789,Human_Splice_Rec_2005796,Human_Splice_Rec_2005797,Human_Splice_Rec_2005804,Human_Splice_Rec_2005805,Human_Splice_Rec_2005810,Human_Splice_Rec_2005811,Human_Splice_Rec_2005820,Human_Splice_Rec_2005827 RMVar_hsa_circ_79650,RMVar_hsa_circ_88795,RMVar_hsa_circ_194750,RMVar_hsa_circ_194749,RMVar_hsa_circ_34356,RMVar_hsa_circ_94339,RMVar_hsa_circ_24237,RMVar_hsa_circ_194756 84332 RMVar_ID_84332 Human_SNP_ID_665538627 m1A Human chr19 + 39435721 39435721 39435721 GCCACAGCTGTCGCTGTCTTCTGTAAGATACAAGAGAAACAGGGGCCCCGTGAGCTCCGGCTCCA GCCACAGCTGTCGCTGTCTTCTGTAAGATACATGAGAAACAGGGGCCCCGTGAGCTCCGGCTCCA A T - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:39435714..39435856 26863410 MeRIP-seq:(Medium) rs1320443767 Functional Loss SNV dbSNP153 33..33 33 - - - 84333 RMVar_ID_84333 Human_SNP_ID_665538695 m1A Human chr19 + 39435830 39435830 39435830 GACCCTGGCCTTCTCCTTCCCCTCCCCTTCCCATCCGGCGTCTGGCTCACCTTGCGTCCGAAGAC GACCCTGGCCTTCTCCTTCCCCTCCCCTTCCCCTCCGGCGTCTGGCTCACCTTGCGTCCGAAGAC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:39435826..39435850 26863196 MeRIP-seq:(Medium) rs564071684 Functional Loss SNV dbSNP153 33..33 33 - - - 84334 RMVar_ID_84334 Human_SNP_ID_665538726 m1A Human chr19 - 39435885 39435885 39435885 TGTCTAGTCCACGCTCGGAGCCATGCCGTCCAAGGGCCCGCTGCAGTCTGTGCAGGTCTTCGGAC TGTCTAGTCCACGCTCGGAGCCATGCCGTCCATGGGCCCGCTGCAGTCTGTGCAGGTCTTCGGAC T A RPS16 Ensembl:ENSG00000105193 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr19:39435563..39435903;chr19:39435651..39435900 26863410 MeRIP-seq:(Medium) rs750866168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55654,Human_RBP_ID_239611,Human_RBP_ID_521737,Human_RBP_ID_770666,Human_RBP_ID_825162,Human_RBP_ID_912738,Human_RBP_ID_1015964,Human_RBP_ID_1189767,Human_RBP_ID_1373316,Human_RBP_ID_1564929,Human_RBP_ID_1887507,Human_RBP_ID_3571673,Human_RBP_ID_4527773,Human_RBP_ID_5145212,Human_RBP_ID_5443100,Human_RBP_ID_5468784,Human_RBP_ID_6761787,Human_RBP_ID_8256113,Human_RBP_ID_8487264,Human_RBP_ID_8833944,Human_RBP_ID_9328934,Human_RBP_ID_13453761,Human_RBP_ID_17269088,Human_RBP_ID_17386829,Human_RBP_ID_17656135,Human_RBP_ID_17695696,Human_RBP_ID_18192256,Human_RBP_ID_18732444,Human_RBP_ID_22447751,Human_RBP_ID_22972532,Human_RBP_ID_23131266,Human_RBP_ID_23797106,Human_RBP_ID_26468203,Human_RBP_ID_26815858,Human_RBP_ID_26989861 Human_Splice_Rec_2005787,Human_Splice_Rec_2005795,Human_Splice_Rec_2005803,Human_Splice_Rec_2005809,Human_Splice_Rec_2005819 RMVar_hsa_circ_88795,RMVar_hsa_circ_194749,RMVar_hsa_circ_34356,RMVar_hsa_circ_24237 84335 RMVar_ID_84335 Human_SNP_ID_665538727 m1A Human chr19 - 39435885 39435885 39435885 TGTCTAGTCCACGCTCGGAGCCATGCCGTCCAAGGGCCCGCTGCAGTCTGTGCAGGTCTTCGGAC TGTCTAGTCCACGCTCGGAGCCATGCCGTCCAGGGGCCCGCTGCAGTCTGTGCAGGTCTTCGGAC T C RPS16 Ensembl:ENSG00000105193 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr19:39435563..39435903;chr19:39435651..39435900 26863410 MeRIP-seq:(Medium) rs750866168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55654,Human_RBP_ID_239611,Human_RBP_ID_521737,Human_RBP_ID_770666,Human_RBP_ID_825162,Human_RBP_ID_912738,Human_RBP_ID_1015964,Human_RBP_ID_1189767,Human_RBP_ID_1373316,Human_RBP_ID_1564929,Human_RBP_ID_1887507,Human_RBP_ID_3571673,Human_RBP_ID_4527773,Human_RBP_ID_5145212,Human_RBP_ID_5443100,Human_RBP_ID_5468784,Human_RBP_ID_6761787,Human_RBP_ID_8256113,Human_RBP_ID_8487264,Human_RBP_ID_8833944,Human_RBP_ID_9328934,Human_RBP_ID_13453761,Human_RBP_ID_17269088,Human_RBP_ID_17386829,Human_RBP_ID_17656135,Human_RBP_ID_17695696,Human_RBP_ID_18192256,Human_RBP_ID_18732444,Human_RBP_ID_22447751,Human_RBP_ID_22972532,Human_RBP_ID_23131266,Human_RBP_ID_23797106,Human_RBP_ID_26468203,Human_RBP_ID_26815858,Human_RBP_ID_26989861 Human_Splice_Rec_2005787,Human_Splice_Rec_2005795,Human_Splice_Rec_2005803,Human_Splice_Rec_2005809,Human_Splice_Rec_2005819 RMVar_hsa_circ_88795,RMVar_hsa_circ_194749,RMVar_hsa_circ_34356,RMVar_hsa_circ_24237 84336 RMVar_ID_84336 Human_SNP_ID_665542014 m1A Human chr19 + 39445937 39445937 39445937 GGACAGCAACTTTTCCGAGGAGGAGGACAGCGAGCGCAGCAGTGACGGCGAGGAGGCCGAGGTCT GGACAGCAACTTTTCCGAGGAGGAGGACAGCGGGCGCAGCAGTGACGGCGAGGAGGCCGAGGTCT A G SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:39445801..39445975 26863196 MeRIP-seq:(Medium) rs754205658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238935,Human_RBP_ID_825777,Human_RBP_ID_913941,Human_RBP_ID_5585700,Human_RBP_ID_6761810,Human_RBP_ID_9328935,Human_RBP_ID_9380996,Human_RBP_ID_13453783,Human_RBP_ID_22977918,Human_RBP_ID_24545481,Human_RBP_ID_26336256 Human_Splice_Rec_2005839,Human_Splice_Rec_2005849,Human_Splice_Rec_2005907,Human_Splice_Rec_2005962,Human_Splice_Rec_2005963,Human_Splice_Rec_2005969,Human_Splice_Rec_2005975,Human_Splice_Rec_2006032,Human_Splice_Rec_2006033,Human_Splice_Rec_2006038,Human_Splice_Rec_2006039,Human_Splice_Rec_2006043,Human_Splice_Rec_2006097 RMVar_hsa_circ_26207,RMVar_hsa_circ_194757,RMVar_hsa_circ_34531,RMVar_hsa_circ_371417 84337 RMVar_ID_84337 Human_SNP_ID_665543907 m1A Human chr19 + 39453260 39453260 39453260 TATATGCAGAGCAAAGTGGGCTATGATTGGCCAGGCCAATCTGAGGTCAGATTTAGGGTGAGGAA TATATGCAGAGCAAAGTGGGCTATGATTGGCCGGGCCAATCTGAGGTCAGATTTAGGGTGAGGAA A G SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:39453257..39453491 26863196 MeRIP-seq:(Medium) rs1465448735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194757,RMVar_hsa_circ_34531,RMVar_hsa_circ_371417 84338 RMVar_ID_84338 Human_SNP_ID_665543911 m1A Human chr19 - 39453306 39453306 39453306 GGTTGTAGCACCAGAATTCTGCTACCCCAAAAATCCAAAAACCAAGTTCCTCACCCTAAATCTGA GGTTGTAGCACCAGAATTCTGCTACCCCAAAAGTCCAAAAACCAAGTTCCTCACCCTAAATCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39453304..39453558 26863196 MeRIP-seq:(Medium) rs1224351025 Functional Loss SNV dbSNP153 33..33 33 - - - 84339 RMVar_ID_84339 Human_SNP_ID_665543937 m1A Human chr19 + 39453363 39453363 39453363 CTACAACCCTGCCTGACCCCTGTAGGTAGACGAAGAGCGGCGGAGTGCAGCGGGCAGTGAGAAAG CTACAACCCTGCCTGACCCCTGTAGGTAGACGTAGAGCGGCGGAGTGCAGCGGGCAGTGAGAAAG A T SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr19:39445576..39457782;chr19:39453351..39453525;chr19:39445576..39457799 26863196 MeRIP-seq:(Medium) rs1396685982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238936,Human_RBP_ID_825687,Human_RBP_ID_6761826,Human_RBP_ID_22977473,Human_RBP_ID_24545483,Human_RBP_ID_26336258,Human_RBP_ID_27816428 Human_Splice_Rec_2005840,Human_Splice_Rec_2005850,Human_Splice_Rec_2005908,Human_Splice_Rec_2005964,Human_Splice_Rec_2005970,Human_Splice_Rec_2005976,Human_Splice_Rec_2006034,Human_Splice_Rec_2006040,Human_Splice_Rec_2006044,Human_Splice_Rec_2006098 RMVar_hsa_circ_194759,RMVar_hsa_circ_85628,RMVar_hsa_circ_194757,RMVar_hsa_circ_34531,RMVar_hsa_circ_371417,RMVar_hsa_circ_295682,RMVar_hsa_circ_54251,RMVar_hsa_circ_194758 84340 RMVar_ID_84340 Human_SNP_ID_665545245 m1A Human chr19 + 39457631 39457631 39457631 CAGAGGAGATGCTTCGTGTCCTGGGAGCTGTTATGAGGTCACCTTTGCCACTTACCACTTGGCCT CAGAGGAGATGCTTCGTGTCCTGGGAGCTGTTGTGAGGTCACCTTTGCCACTTACCACTTGGCCT A G SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39457628..39457796 26863196 MeRIP-seq:(Medium) rs376588225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194759,RMVar_hsa_circ_85628,RMVar_hsa_circ_194757,RMVar_hsa_circ_34531,RMVar_hsa_circ_371417,RMVar_hsa_circ_54251,RMVar_hsa_circ_194760 84341 RMVar_ID_84341 Human_SNP_ID_665545246 m1A Human chr19 + 39457631 39457631 39457631 CAGAGGAGATGCTTCGTGTCCTGGGAGCTGTTATGAGGTCACCTTTGCCACTTACCACTTGGCCT CAGAGGAGATGCTTCGTGTCCTGGGAGCTGTTTTGAGGTCACCTTTGCCACTTACCACTTGGCCT A T SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39457628..39457796 26863196 MeRIP-seq:(Medium) rs376588225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194759,RMVar_hsa_circ_85628,RMVar_hsa_circ_194757,RMVar_hsa_circ_34531,RMVar_hsa_circ_371417,RMVar_hsa_circ_54251,RMVar_hsa_circ_194760 84342 RMVar_ID_84342 Human_SNP_ID_665545507 m1A Human chr19 - 39458279 39458277 39458279 TCTTACCTTCAATCTCTTCTACTTGGAGGAAGAGGAGGTGGTGGTGGTGGTGGTGGTGGTGGTGG TCTTACCTTCAATCTCTTCTACTTGGAGGAAG__GAGGTGGTGGTGGTGGTGGTGGTGGTGGTGG CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:39458276..39458325 26863196 MeRIP-seq:(Medium) rs752871750 Functional Loss DEL dbSNP153 33..34 33 - - - 84343 RMVar_ID_84343 Human_SNP_ID_665548734 m1A Human chr19 + 39470185 39470185 39470185 AATACTTCAAGATGGGGGACCACGTGAAGGTGATTGCTGGCCGATTCGAGGGCGACACAGGCCTC AATACTTCAAGATGGGGGACCACGTGAAGGTGGTTGCTGGCCGATTCGAGGGCGACACAGGCCTC A G SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39470088..39470184 26863196 MeRIP-seq:(Medium) rs1425785145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54670,Human_RBP_ID_772276,Human_RBP_ID_907739,Human_RBP_ID_1373326,Human_RBP_ID_1887548,Human_RBP_ID_3571687,Human_RBP_ID_3955015,Human_RBP_ID_6761910,Human_RBP_ID_8833975,Human_RBP_ID_9087873,Human_RBP_ID_9293677,Human_RBP_ID_18732499,Human_RBP_ID_23797149,Human_RBP_ID_24374929,Human_RBP_ID_26989898,Human_RBP_ID_27815436 Human_Splice_Rec_2005878,Human_Splice_Rec_2005879,Human_Splice_Rec_2005934,Human_Splice_Rec_2005935,Human_Splice_Rec_2006004,Human_Splice_Rec_2006005,Human_Splice_Rec_2006070,Human_Splice_Rec_2006071,Human_Splice_Rec_2006126,Human_Splice_Rec_2006127,Human_Splice_Rec_2006202,Human_Splice_Rec_2006203,Human_Splice_Rec_2006225 RMVar_hsa_circ_106071,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763,RMVar_hsa_circ_65966,RMVar_hsa_circ_122015,RMVar_hsa_circ_103437,RMVar_hsa_circ_194765,RMVar_hsa_circ_123595,RMVar_hsa_circ_194767,RMVar_hsa_circ_194769,RMVar_hsa_circ_113545,RMVar_hsa_circ_194768 84344 RMVar_ID_84344 Human_SNP_ID_665549054 m1A Human chr19 + 39471421 39471421 39471421 CAGACATCAGGCTGTGACCCGGAAGAAGGACAACCGCTTTGCTGTGGCCTTGGACTCAGAGCAGA CAGACATCAGGCTGTGACCCGGAAGAAGGACAGCCGCTTTGCTGTGGCCTTGGACTCAGAGCAGA A G SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39471371..39471472 32194978 MeRIP-seq:(Medium) rs758041067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280167,Human_RBP_ID_1564998,Human_RBP_ID_1887554,Human_RBP_ID_3955020,Human_RBP_ID_5585709,Human_RBP_ID_6761917,Human_RBP_ID_8833988,Human_RBP_ID_9293679,Human_RBP_ID_13454008,Human_RBP_ID_17269090,Human_RBP_ID_18732506,Human_RBP_ID_22071629 Human_Splice_Rec_2005882,Human_Splice_Rec_2005883,Human_Splice_Rec_2005938,Human_Splice_Rec_2005939,Human_Splice_Rec_2006008,Human_Splice_Rec_2006009,Human_Splice_Rec_2006074,Human_Splice_Rec_2006075,Human_Splice_Rec_2006130,Human_Splice_Rec_2006131,Human_Splice_Rec_2006206,Human_Splice_Rec_2006207,Human_Splice_Rec_2006227 Human_miRNA_ID_2255687,Human_miRNA_ID_2883490 RMVar_hsa_circ_106071,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763,RMVar_hsa_circ_65966,RMVar_hsa_circ_122015,RMVar_hsa_circ_103437,RMVar_hsa_circ_194765,RMVar_hsa_circ_123595,RMVar_hsa_circ_194767,RMVar_hsa_circ_194769,RMVar_hsa_circ_113545,RMVar_hsa_circ_194768 84345 RMVar_ID_84345 Human_SNP_ID_665549600 m1A Human chr19 + 39473265 39473244 39473265 GACCTATGGGAGGACGCCCATGTATGGCTCCCAGACGCCCATGTATGGCTCTGGCTCCCGAACAC GACCTATGGGAG_____________________GACGCCCATGTATGGCTCTGGCTCCCGAACAC GGACGCCCATGTATGGCTCCCA G SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39473132..39473350 26863196 MeRIP-seq:(Medium) rs1486206860 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_54678,Human_RBP_ID_240771,Human_RBP_ID_8487305,Human_RBP_ID_9294424,Human_RBP_ID_18732516,Human_RBP_ID_22810835 Human_Splice_Rec_2005892,Human_Splice_Rec_2005893,Human_Splice_Rec_2005948,Human_Splice_Rec_2005949,Human_Splice_Rec_2006018,Human_Splice_Rec_2006019,Human_Splice_Rec_2006084,Human_Splice_Rec_2006085,Human_Splice_Rec_2006140,Human_Splice_Rec_2006141,Human_Splice_Rec_2006216,Human_Splice_Rec_2006217 RMVar_hsa_circ_106071,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763,RMVar_hsa_circ_122015,RMVar_hsa_circ_103437,RMVar_hsa_circ_194765,RMVar_hsa_circ_123595,RMVar_hsa_circ_194767,RMVar_hsa_circ_194769,RMVar_hsa_circ_113545,RMVar_hsa_circ_194768,RMVar_hsa_circ_119853,RMVar_hsa_circ_194771 84346 RMVar_ID_84346 Human_SNP_ID_665549618 m1A Human chr19 + 39473293 39473293 39473293 TCCCAGACGCCCATGTATGGCTCTGGCTCCCGAACACCCATGTACGGCTCACAGACACCCCTCCA TCCCAGACGCCCATGTATGGCTCTGGCTCCCGGACACCCATGTACGGCTCACAGACACCCCTCCA A G SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39473168..39473300 26863196 MeRIP-seq:(Medium) rs778281382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521751,Human_RBP_ID_1565006,Human_RBP_ID_6761926,Human_RBP_ID_8833998,Human_RBP_ID_9294424,Human_RBP_ID_13454011 Human_Splice_Rec_2005892,Human_Splice_Rec_2005893,Human_Splice_Rec_2005948,Human_Splice_Rec_2005949,Human_Splice_Rec_2006018,Human_Splice_Rec_2006019,Human_Splice_Rec_2006084,Human_Splice_Rec_2006085,Human_Splice_Rec_2006140,Human_Splice_Rec_2006141,Human_Splice_Rec_2006216,Human_Splice_Rec_2006217 RMVar_hsa_circ_106071,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763,RMVar_hsa_circ_122015,RMVar_hsa_circ_103437,RMVar_hsa_circ_194765,RMVar_hsa_circ_123595,RMVar_hsa_circ_194767,RMVar_hsa_circ_194769,RMVar_hsa_circ_113545,RMVar_hsa_circ_194768,RMVar_hsa_circ_119853,RMVar_hsa_circ_194771 84347 RMVar_ID_84347 Human_SNP_ID_665549624 m1A Human chr19 + 39473311 39473311 39473311 GGCTCTGGCTCCCGAACACCCATGTACGGCTCACAGACACCCCTCCAGGATGGTGAGTGCCCGCA GGCTCTGGCTCCCGAACACCCATGTACGGCTCCCAGACACCCCTCCAGGATGGTGAGTGCCCGCA A C SUPT5H Ensembl:ENSG00000196235 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:39473186..39473404 26863196 MeRIP-seq:(Medium) rs145017682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521751,Human_RBP_ID_913970,Human_RBP_ID_1015978,Human_RBP_ID_5370377,Human_RBP_ID_6761926,Human_RBP_ID_9294424 Human_Splice_Rec_2005893,Human_Splice_Rec_2005949,Human_Splice_Rec_2006019,Human_Splice_Rec_2006085,Human_Splice_Rec_2006141,Human_Splice_Rec_2006217 Human_miRNA_ID_2153905,Human_miRNA_ID_2673457,Human_miRNA_ID_2801781,Human_miRNA_ID_3009913 RMVar_hsa_circ_106071,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763,RMVar_hsa_circ_122015,RMVar_hsa_circ_103437,RMVar_hsa_circ_194765,RMVar_hsa_circ_123595,RMVar_hsa_circ_194767,RMVar_hsa_circ_194769,RMVar_hsa_circ_113545,RMVar_hsa_circ_194768,RMVar_hsa_circ_119853,RMVar_hsa_circ_194771 84348 RMVar_ID_84348 Human_SNP_ID_665549826 m1A Human chr19 - 39474023 39474023 39474023 TAGCCAGGTGTTTGGGGATTGGGGGTTCCCCCATAGGCCTGCGGGGACGGGGTGGGCTCATCATC TAGCCAGGTGTTTGGGGATTGGGGGTTCCCCCGTAGGCCTGCGGGGACGGGGTGGGCTCATCATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39473975..39474548 26863196 MeRIP-seq:(Medium) rs768699106 Functional Loss SNV dbSNP153 33..33 33 - - - 84349 RMVar_ID_84349 Human_SNP_ID_665550271 m1A Human chr19 - 39475375 39475375 39475375 ATTTTTTTTTTTTTGAGGAGTCTTGCTCTGTCACCCAGACTGGGGCGCAGTGGCACGATCTCGGC ATTTTTTTTTTTTTGAGGAGTCTTGCTCTGTCCCCCAGACTGGGGCGCAGTGGCACGATCTCGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39475373..39475841 26863196 MeRIP-seq:(Medium) rs1208757357 Functional Loss SNV dbSNP153 33..33 33 - - - 84350 RMVar_ID_84350 Human_SNP_ID_665552141 m1A Human chr19 + 39480889 39480889 39480889 GCGGCCTCGGCAGCGGTGTTCTCGCGCTTGCGAAGCGGGCTCCGGCTCGGCTCGCGGGGACTGTG GCGGCCTCGGCAGCGGTGTTCTCGCGCTTGCGGAGCGGGCTCCGGCTCGGCTCGCGGGGACTGTG A G TIMM50 Ensembl:ENSG00000105197 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39480826..39481004 26863196 MeRIP-seq:(Medium) rs112385179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280186,Human_RBP_ID_4558441,Human_RBP_ID_5117489,Human_RBP_ID_5376665,Human_RBP_ID_22448724 Human_Splice_Rec_2006231,Human_Splice_Rec_2006251,Human_Splice_Rec_2006269,Human_Splice_Rec_2006289,Human_Splice_Rec_2006295,Human_Splice_Rec_2006299,Human_Splice_Rec_2006311,Human_Splice_Rec_2006323,Human_Splice_Rec_2006335,Human_Splice_Rec_2006341,Human_Splice_Rec_2006351,Human_Splice_Rec_2006365 84351 RMVar_ID_84351 Human_SNP_ID_665552146 m1A Human chr19 - 39480897 39480897 39480897 ACCTCGTGCACAGTCCCCGCGAGCCGAGCCGGAGCCCGCTTCGCAAGCGCGAGAACACCGCTGCC ACCTCGTGCACAGTCCCCGCGAGCCGAGCCGGGGCCCGCTTCGCAAGCGCGAGAACACCGCTGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:39480851..39480993;chr19:39480851..39481015 26863196 MeRIP-seq:(Medium) rs544975086 Functional Loss SNV dbSNP153 33..33 33 - - - 84352 RMVar_ID_84352 Human_SNP_ID_665552147 m1A Human chr19 - 39480897 39480897 39480897 ACCTCGTGCACAGTCCCCGCGAGCCGAGCCGGAGCCCGCTTCGCAAGCGCGAGAACACCGCTGCC ACCTCGTGCACAGTCCCCGCGAGCCGAGCCGGCGCCCGCTTCGCAAGCGCGAGAACACCGCTGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:39480851..39480993;chr19:39480851..39481015 26863196 MeRIP-seq:(Medium) rs544975086 Functional Loss SNV dbSNP153 33..33 33 - - - 84353 RMVar_ID_84353 Human_SNP_ID_665567704 m1A Human chr19 - 39532751 39532751 39532751 TGTTGGAGATGTCCGAGCTCCCCGGAGATAGCAGTGTCCCACAGGTGGGCACCGCGAGTGGCGTC TGTTGGAGATGTCCGAGCTCCCCGGAGATAGCCGTGTCCCACAGGTGGGCACCGCGAGTGGCGTC T G EID2B Ensembl:ENSG00000176401 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39532705..39532789 26863196 MeRIP-seq:(Medium) rs1313287098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565081,Human_RBP_ID_4528174 Human_Splice_Rec_2006497 84354 RMVar_ID_84354 Human_SNP_ID_665567711 m1A Human chr19 + 39532765 39532765 39532765 TGCCCACCTGTGGGACACTGCTATCTCCGGGGAGCTCGGACATCTCCAACAGCCCAGTCGGCTCC TGCCCACCTGTGGGACACTGCTATCTCCGGGGTGCTCGGACATCTCCAACAGCCCAGTCGGCTCC A T AC011500.3 Ensembl:ENSG00000269792 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39532714..39532790 26863196 MeRIP-seq:(Medium) rs1254173064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2006499 84355 RMVar_ID_84355 Human_SNP_ID_665567723 m1A Human chr19 - 39532790 39532790 39532790 TCCGTAGAAACGCTGGGACTATGGCGGAGCCGACTGGGCTGTTGGAGATGTCCGAGCTCCCCGGA TCCGTAGAAACGCTGGGACTATGGCGGAGCCGCCTGGGCTGTTGGAGATGTCCGAGCTCCCCGGA T G EID2B Ensembl:ENSG00000176401 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39532608..39532810 26863196 MeRIP-seq:(Medium) rs1433927657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2006497 84356 RMVar_ID_84356 Human_SNP_ID_665569519 m1A Human chr19 + 39539830 39539809 39539830 GCTTTCCCTGCCCGCCGCGGCTGCCCTGGCCAACGCCGCCGCTGCCACCGGGGCTCCCCTGGCTG GCTTTCCCTGCC_____________________CGCCGCCGCTGCCACCGGGGCTCCCCTGGCTG CCGCCGCGGCTGCCCTGGCCAA C lnc-SELENOV-4 RNACentral:URS00008B786B lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:39539780..39540050 26863196 MeRIP-seq:(Medium) rs767335073 Functional Loss DEL dbSNP153 13..33 33 - - - 84357 RMVar_ID_84357 Human_SNP_ID_665569534 m1A Human chr19 + 39539830 39539830 39539830 GCTTTCCCTGCCCGCCGCGGCTGCCCTGGCCAACGCCGCCGCTGCCACCGGGGCTCCCCTGGCTG GCTTTCCCTGCCCGCCGCGGCTGCCCTGGCCATCGCCGCCGCTGCCACCGGGGCTCCCCTGGCTG A T lnc-SELENOV-4 RNACentral:URS00008B786B lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:39539780..39540050 26863196 MeRIP-seq:(Medium) rs756864090 Functional Loss SNV dbSNP153 33..33 33 - - - 84358 RMVar_ID_84358 Human_SNP_ID_665569590 m1A Human chr19 - 39539929 39539929 39539929 AGGAGGCCGGGGAAGGCGCGATGGCGGCGGCCAGGGGAGGCCCGGTGCCGGCGGCCAGGGAAGGT AGGAGGCCGGGGAAGGCGCGATGGCGGCGGCCGGGGGAGGCCCGGTGCCGGCGGCCAGGGAAGGT T C EID2 Ensembl:ENSG00000176396 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39539660..39540134 26863196 MeRIP-seq:(Medium) rs773534199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9353729,Human_RBP_ID_22447754 84359 RMVar_ID_84359 Human_SNP_ID_665640487 m1A Human chr19 - 39818103 39818103 39818103 GGTTGGGGCCAGGATAGGGGAGCCACAGGGGGACTGTGGGAGCCAGAGGCAGCTCCTGACCCAGT GGTTGGGGCCAGGATAGGGGAGCCACAGGGGGGCTGTGGGAGCCAGAGGCAGCTCCTGACCCAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39818092..39818184 26863196 MeRIP-seq:(Medium) rs1385272029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6762351,Human_RBP_ID_8834065,Human_RBP_ID_18732629 84360 RMVar_ID_84360 Human_SNP_ID_665640729 m1A Human chr19 + 39819076 39819076 39819076 CTCACGGGCCTCCCTGCTCTCATTCTCAGCCCACACTTCCATCTATACACCCTCCCTTAGTGATC CTCACGGGCCTCCCTGCTCTCATTCTCAGCCCCCACTTCCATCTATACACCCTCCCTTAGTGATC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39818907..39819213 26863196 MeRIP-seq:(Medium) rs1165887471 Functional Loss SNV dbSNP153 33..33 33 - - - 84361 RMVar_ID_84361 Human_SNP_ID_665640841 m1A Human chr19 - 39819574 39819574 39819574 AGGTCAGGTGGGACCGGGAGGCCATGGGAAGGACTTGAATTTGAAGCTGATGAGATGTGTGGCAG AGGTCAGGTGGGACCGGGAGGCCATGGGAAGGGCTTGAATTTGAAGCTGATGAGATGTGTGGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39819523..39819666 26863196 MeRIP-seq:(Medium) rs984925255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6762409,Human_RBP_ID_13454824,Human_RBP_ID_17924801,Human_RBP_ID_18305226,Human_RBP_ID_25416335 84362 RMVar_ID_84362 Human_SNP_ID_665642729 m1A Human chr19 - 39825874 39825874 39825874 AGCCTGGTGGGCGGCCCTGCTGACTGCTCCCCACCTCACCCAGCGCCTGCCCCCCAGCACCCGGC AGCCTGGTGGGCGGCCCTGCTGACTGCTCCCCGCCTCACCCAGCGCCTGCCCCCCAGCACCCGGC T C DYRK1B Ensembl:ENSG00000105204 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:39825775..39826009 26863196 MeRIP-seq:(Medium) rs1033741194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521861,Human_RBP_ID_27468131 Human_miRNA_ID_842982,Human_miRNA_ID_2007808,Human_miRNA_ID_2007809,Human_miRNA_ID_2368303,Human_miRNA_ID_2368304,Human_miRNA_ID_2726633,Human_miRNA_ID_2726634,Human_miRNA_ID_3016086,Human_miRNA_ID_3016087 RMVar_hsa_circ_99259,RMVar_hsa_circ_124930,RMVar_hsa_circ_108767,RMVar_hsa_circ_194780,RMVar_hsa_circ_194782,RMVar_hsa_circ_89255,RMVar_hsa_circ_194781,RMVar_hsa_circ_194779 84363 RMVar_ID_84363 Human_SNP_ID_665645163 m1A Human chr19 - 39833144 39833142 39833144 GTCGTGGAGTGGCAAGGCATGGAATAGGAGAAAGGGATTTGACATGGGGGAGAGAGTGGCCCATG GTCGTGGAGTGGCAAGGCATGGAATAGGAGAA__GGATTTGACATGGGGGAGAGAGTGGCCCATG CCT C DYRK1B Ensembl:ENSG00000105204 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39833094..39833246 26863196 MeRIP-seq:(Medium) rs1464839970 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22591891 84364 RMVar_ID_84364 Human_SNP_ID_665645549 m1A Human chr19 + 39834089 39834089 39834089 GGGAGCCCGAGCTCAGACCTGCCCACTGGCTGAGGGTATCCGGCGGACGCGGCAAGCCAGGGCCC GGGAGCCCGAGCTCAGACCTGCCCACTGGCTGCGGGTATCCGGCGGACGCGGCAAGCCAGGGCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39834038..39834114 26863196 MeRIP-seq:(Medium) rs1204176404 Functional Loss SNV dbSNP153 33..33 33 - - - 84365 RMVar_ID_84365 Human_SNP_ID_665645719 m1A Human chr19 + 39834527 39834527 39834527 CAGTATCAACACACATCTCTCGCAATCCTGACAGCGCTGAACTTCAGTTCTTCACCTTGGGGGGT CAGTATCAACACACATCTCTCGCAATCCTGACGGCGCTGAACTTCAGTTCTTCACCTTGGGGGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39834476..39834855 26863196 MeRIP-seq:(Medium) rs779293864 Functional Loss SNV dbSNP153 33..33 33 - - - 84366 RMVar_ID_84366 Human_SNP_ID_665645720 m1A Human chr19 + 39834527 39834527 39834527 CAGTATCAACACACATCTCTCGCAATCCTGACAGCGCTGAACTTCAGTTCTTCACCTTGGGGGGT CAGTATCAACACACATCTCTCGCAATCCTGACTGCGCTGAACTTCAGTTCTTCACCTTGGGGGGT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:39834476..39834855 26863196 MeRIP-seq:(Medium) rs779293864 Functional Loss SNV dbSNP153 33..33 33 - - - 84367 RMVar_ID_84367 Human_SNP_ID_665645730 m1A Human chr19 + 39834548 39834548 39834548 GCAATCCTGACAGCGCTGAACTTCAGTTCTTCACCTTGGGGGGTGGCCTGTGAGAGGAAGATAGG GCAATCCTGACAGCGCTGAACTTCAGTTCTTCGCCTTGGGGGGTGGCCTGTGAGAGGAAGATAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39834476..39834575 32194978 MeRIP-seq:(Medium) rs1006839040 Functional Loss SNV dbSNP153 33..33 33 - - - 84368 RMVar_ID_84368 Human_SNP_ID_665645815 m1A Human chr19 + 39834720 39834720 39834720 GGCATGGTCTCTTTCATATGGCTCAAGGGTCAACTGCTCCTGCGGCTTCATGTTCTCCTGTTGCA GGCATGGTCTCTTTCATATGGCTCAAGGGTCAGCTGCTCCTGCGGCTTCATGTTCTCCTGTTGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39834651..39834750 32194978 MeRIP-seq:(Medium) rs1346481870 Functional Loss SNV dbSNP153 33..33 33 - - - 84369 RMVar_ID_84369 Human_SNP_ID_665646574 m1A Human chr19 - 39837845 39837845 39837845 GCATCACTGTTCATTAATTTTTAATTTATTTTAGGATGGTCTAGTCTATGCAGTCGAGTTCTCCC GCATCACTGTTCATTAATTTTTAATTTATTTTCGGATGGTCTAGTCTATGCAGTCGAGTTCTCCC T G FBL Ensembl:ENSG00000105202 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39837801..39837850 32194978 MeRIP-seq:(Medium) rs112828701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6762661,Human_RBP_ID_13455288 RMVar_hsa_circ_112647,RMVar_hsa_circ_89668,RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_85011,RMVar_hsa_circ_194788,RMVar_hsa_circ_194787,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_80056,RMVar_hsa_circ_194796,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194798 84370 RMVar_ID_84370 Human_SNP_ID_665646875 m1A Human chr19 - 39838967 39838967 39838967 AGGCTGCCTCCCTTCTGCCAACCTGGAATATCAGGGTTTGACTGCTTGCCTGCGCTGTGTGACTT AGGCTGCCTCCCTTCTGCCAACCTGGAATATCGGGGTTTGACTGCTTGCCTGCGCTGTGTGACTT T C FBL Ensembl:ENSG00000105202 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:39838962..39839098 26863196 MeRIP-seq:(Medium) rs1241918233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565313,Human_RBP_ID_6762681,Human_RBP_ID_13455327,Human_RBP_ID_23797423 RMVar_hsa_circ_112647,RMVar_hsa_circ_89668,RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_85011,RMVar_hsa_circ_194788,RMVar_hsa_circ_194787,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_80056,RMVar_hsa_circ_194796,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194798 84371 RMVar_ID_84371 Human_SNP_ID_665646940 m1A Human chr19 - 39839126 39839126 39839126 CAAGCTAGCAGCAGCAATCCTGGGTGGTGTGGACCAGATCCACATCAAACCGGGGGCTAAGGTTC CAAGCTAGCAGCAGCAATCCTGGGTGGTGTGGGCCAGATCCACATCAAACCGGGGGCTAAGGTTC T C FBL Ensembl:ENSG00000105202 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:39839076..39839150;chr19:39839026..39839200 26863196 MeRIP-seq:(Medium) rs749684178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521889,Human_RBP_ID_1016107,Human_RBP_ID_1565318,Human_RBP_ID_1887712,Human_RBP_ID_6762685,Human_RBP_ID_8834180,Human_RBP_ID_18441381,Human_RBP_ID_18732740,Human_RBP_ID_22446749,Human_RBP_ID_22502897 Human_Splice_Rec_2006748,Human_Splice_Rec_2006749,Human_Splice_Rec_2006762,Human_Splice_Rec_2006763,Human_Splice_Rec_2006782,Human_Splice_Rec_2006783,Human_Splice_Rec_2006796,Human_Splice_Rec_2006797,Human_Splice_Rec_2006808,Human_Splice_Rec_2006809,Human_Splice_Rec_2006820,Human_Splice_Rec_2006821,Human_Splice_Rec_2006832,Human_Splice_Rec_2006833,Human_Splice_Rec_2006842,Human_Splice_Rec_2006850,Human_Splice_Rec_2006858 RMVar_hsa_circ_112647,RMVar_hsa_circ_89668,RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_85011,RMVar_hsa_circ_194788,RMVar_hsa_circ_194787,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_80056,RMVar_hsa_circ_194796,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194798,RMVar_hsa_circ_32874 84372 RMVar_ID_84372 Human_SNP_ID_665647289 m1A Human chr19 - 39840438 39840438 39840438 GAAAAAGAGGAAACCAGTCGGGGAAGAATGTGATGGTGGAGCCGCATCGGCATGAGGGTGAGTGA GAAAAAGAGGAAACCAGTCGGGGAAGAATGTGGTGGTGGAGCCGCATCGGCATGAGGGTGAGTGA T C FBL Ensembl:ENSG00000105202 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:39840251..39846315 26863410 MeRIP-seq:(Medium) rs1447588322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521896,Human_RBP_ID_913609,Human_RBP_ID_1016111,Human_RBP_ID_1189854,Human_RBP_ID_1294368,Human_RBP_ID_1565326,Human_RBP_ID_1887716,Human_RBP_ID_3571824,Human_RBP_ID_3955029,Human_RBP_ID_4528423,Human_RBP_ID_5116259,Human_RBP_ID_5320367,Human_RBP_ID_6762694,Human_RBP_ID_8487562,Human_RBP_ID_9330036,Human_RBP_ID_9353731,Human_RBP_ID_17655353,Human_RBP_ID_18412539,Human_RBP_ID_18441383,Human_RBP_ID_18470727,Human_RBP_ID_18732747,Human_RBP_ID_18997822,Human_RBP_ID_22071972,Human_RBP_ID_22449463,Human_RBP_ID_22978107,Human_RBP_ID_23131306,Human_RBP_ID_23797428,Human_RBP_ID_26336288,Human_RBP_ID_26989999 Human_Splice_Rec_2006745,Human_Splice_Rec_2006758,Human_Splice_Rec_2006759,Human_Splice_Rec_2006780,Human_Splice_Rec_2006781,Human_Splice_Rec_2006792,Human_Splice_Rec_2006793,Human_Splice_Rec_2006805,Human_Splice_Rec_2006817,Human_Splice_Rec_2006828,Human_Splice_Rec_2006829,Human_Splice_Rec_2006838,Human_Splice_Rec_2006839,Human_Splice_Rec_2006846,Human_Splice_Rec_2006847,Human_Splice_Rec_2006854,Human_Splice_Rec_2006855 Human_miRNA_ID_2023057,Human_miRNA_ID_2023058,Human_miRNA_ID_2261593,Human_miRNA_ID_2261594,Human_miRNA_ID_2264647,Human_miRNA_ID_2264648,Human_miRNA_ID_2267712,Human_miRNA_ID_2267713 RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_30690,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194801,RMVar_hsa_circ_375114,RMVar_hsa_circ_194802,RMVar_hsa_circ_376972 84373 RMVar_ID_84373 Human_SNP_ID_665647301 m1A Human chr19 - 39840463 39840463 39840463 GGCAACCGGGGTCGTGGTCGGGGAGGAAAAAGAGGAAACCAGTCGGGGAAGAATGTGATGGTGGA GGCAACCGGGGTCGTGGTCGGGGAGGAAAAAGGGGAAACCAGTCGGGGAAGAATGTGATGGTGGA T C FBL Ensembl:ENSG00000105202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:39840197..39846375;chr19:39840401..39840525;chr19:39838990..39846375;chr19:39839026..39846400 26863196 MeRIP-seq:(Medium) rs1208436601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521897,Human_RBP_ID_825600,Human_RBP_ID_907750,Human_RBP_ID_1132947,Human_RBP_ID_1565326,Human_RBP_ID_1887716,Human_RBP_ID_3571825,Human_RBP_ID_3955029,Human_RBP_ID_5117738,Human_RBP_ID_5320367,Human_RBP_ID_6762697,Human_RBP_ID_8487562,Human_RBP_ID_8942446,Human_RBP_ID_9087919,Human_RBP_ID_9353597,Human_RBP_ID_17655353,Human_RBP_ID_17695737,Human_RBP_ID_17924897,Human_RBP_ID_18470727,Human_RBP_ID_18997822,Human_RBP_ID_22071972,Human_RBP_ID_22446751,Human_RBP_ID_22978107,Human_RBP_ID_23131306,Human_RBP_ID_23797428,Human_RBP_ID_26336289,Human_RBP_ID_26468286,Human_RBP_ID_26990000 Human_Splice_Rec_2006745,Human_Splice_Rec_2006758,Human_Splice_Rec_2006759,Human_Splice_Rec_2006780,Human_Splice_Rec_2006781,Human_Splice_Rec_2006793,Human_Splice_Rec_2006805,Human_Splice_Rec_2006817,Human_Splice_Rec_2006828,Human_Splice_Rec_2006829,Human_Splice_Rec_2006838,Human_Splice_Rec_2006839,Human_Splice_Rec_2006846,Human_Splice_Rec_2006847,Human_Splice_Rec_2006854,Human_Splice_Rec_2006855 RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_30690,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194801,RMVar_hsa_circ_375114,RMVar_hsa_circ_194802,RMVar_hsa_circ_376972 84374 RMVar_ID_84374 Human_SNP_ID_665647327 m1A Human chr19 + 39840514 39840514 39840514 CGACCCCGGTTGCCACCAGAATGGAAGCCTCCACCTATAAAGGAGAGGTACAACAGGAGAGAAAG CGACCCCGGTTGCCACCAGAATGGAAGCCTCCCCCTATAAAGGAGAGGTACAACAGGAGAGAAAG A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr19:39840351..39846365 26863410 MeRIP-seq:(Medium) rs1296321775 Functional Loss SNV dbSNP153 33..33 33 - - - 84375 RMVar_ID_84375 Human_SNP_ID_665647461 m1A Human chr19 + 39840764 39840762 39840765 ACCACGGTCACCAAAGCCCCCTCGGCCGCCAAAGCCACCCCCACGGGGACTGAATCCTGTGGGGG ACCACGGTCACCAAAGCCCCCTCGGCCGCCA___CCACCCCCACGGGGACTGAATCCTGTGGGGG AAAG A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:39840713..39846315 32194978 MeRIP-seq:(Medium) rs1392147812 Functional Loss DEL dbSNP153 32..34 33 - - - 84376 RMVar_ID_84376 Human_SNP_ID_665648747 m1A Human chr19 - 39846140 39846140 39846140 CAGTCTCCTGTGGGAAGGGGGATTCTGATTCCAGCAGGTCTAGGGGTTTGTGACTGGCTTCAGAG CAGTCTCCTGTGGGAAGGGGGATTCTGATTCCGGCAGGTCTAGGGGTTTGTGACTGGCTTCAGAG T C FBL Ensembl:ENSG00000105202 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:39846128..39846350 26863196 MeRIP-seq:(Medium) rs1194643287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581200,Human_RBP_ID_5320371,Human_RBP_ID_5370391,Human_RBP_ID_9425329 RMVar_hsa_circ_92207,RMVar_hsa_circ_194784 84377 RMVar_ID_84377 Human_SNP_ID_665648841 m1A Human chr19 - 39846339 39846339 39846339 CGTGCGAAAGCCCCGGACTCGTGGAGTTGTGAACGCCGCGGACTCCGGAGCCGCACAAACCAGGG CGTGCGAAAGCCCCGGACTCGTGGAGTTGTGAGCGCCGCGGACTCCGGAGCCGCACAAACCAGGG T C FBL Ensembl:ENSG00000105202 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr19:39846192..39846375;chr19:39846219..39846375 26863196 MeRIP-seq:(Medium) rs1179477839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521907,Human_RBP_ID_1565332,Human_RBP_ID_3571832,Human_RBP_ID_4557487,Human_RBP_ID_5443109,Human_RBP_ID_8487577,Human_RBP_ID_8834188,Human_RBP_ID_22235016,Human_RBP_ID_23210963 Human_Splice_Rec_2006755,Human_Splice_Rec_2006779,Human_Splice_Rec_2006803,Human_Splice_Rec_2006815,Human_Splice_Rec_2006825,Human_Splice_Rec_2006835,Human_Splice_Rec_2006843,Human_Splice_Rec_2006851 RMVar_hsa_circ_92207,RMVar_hsa_circ_194784 84378 RMVar_ID_84378 Human_SNP_ID_665677230 m1A Human chr19 - 39943691 39943691 39943691 AAGCCCAGGCGGCGGTGGAAAGGCTGGAGGACACACCTAAACATGTGGAATCCCAATGCCGGGCA AAGCCCAGGCGGCGGTGGAAAGGCTGGAGGACGCACCTAAACATGTGGAATCCCAATGCCGGGCA T C lnc-FCGBP-1,lnc-FCGBP-1:2 RNACentral:URS0000D5A1A6,RNACentral:URS00008B50DC lincRNA,lincRNA intron,exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:39943603..39943729 26863410 MeRIP-seq:(Medium) rs1163742590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4568645 84379 RMVar_ID_84379 Human_SNP_ID_665686429 m1A Human chr19 - 39979996 39979996 39979996 ACAAGCCTGTCCAAGACCCCGGGCCTTGTTTCAGCATCACTTACCCCCTGTCTGAGCATCGAATC ACAAGCCTGTCCAAGACCCCGGGCCTTGTTTCGGCATCACTTACCCCCTGTCTGAGCATCGAATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39979994..39980086 26863196 MeRIP-seq:(Medium) rs748637129 Functional Loss SNV dbSNP153 33..33 33 - - - 84380 RMVar_ID_84380 Human_SNP_ID_665686732 m1A Human chr19 - 39981178 39981178 39981178 GGACAGCCAACATTCCACTCTGTTGAAGGATGAGAGTTAAAATCTACTTCCTGTGGCAGGGCACA GGACAGCCAACATTCCACTCTGTTGAAGGATGGGAGTTAAAATCTACTTCCTGTGGCAGGGCACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39981176..39981400 32194978 MeRIP-seq:(Medium) rs765532549 Functional Loss SNV dbSNP153 33..33 33 - - - 84381 RMVar_ID_84381 Human_SNP_ID_665701997 m1A Human chr19 - 40047431 40047431 40047431 CATTTCTAAGCCAGATGTGATTACATTACTAGAGCAAGAGAAAGAGCCCTGGATTGTTGTAAGTA CATTTCTAAGCCAGATGTGATTACATTACTAGGGCAAGAGAAAGAGCCCTGGATTGTTGTAAGTA T C ZNF780B Ensembl:ENSG00000128000 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40047417..40047489 26863196 MeRIP-seq:(Medium) rs1313629841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_912650,Human_RBP_ID_1887956,Human_RBP_ID_13456306,Human_RBP_ID_18997826,Human_RBP_ID_19090167 Human_Splice_Rec_2007124,Human_Splice_Rec_2007125,Human_Splice_Rec_2007132,Human_Splice_Rec_2007133,Human_Splice_Rec_2007142,Human_Splice_Rec_2007143,Human_Splice_Rec_2007150,Human_Splice_Rec_2007151,Human_Splice_Rec_2007158,Human_Splice_Rec_2007159,Human_Splice_Rec_2007166,Human_Splice_Rec_2007174 RMVar_hsa_circ_114747,RMVar_hsa_circ_194813,RMVar_hsa_circ_194817,RMVar_hsa_circ_194814,RMVar_hsa_circ_347697 84382 RMVar_ID_84382 Human_SNP_ID_665736583 m1A Human chr19 + 40191595 40191595 40191595 CGGCCCGGGGCGGCCGCCCCAGGGGCCCCGCCACCCCCGCCCGGCCCGGCAGTCGTGGCCCGGGA CGGCCCGGGGCGGCCGCCCCAGGGGCCCCGCCCCCCCCGCCCGGCCCGGCAGTCGTGGCCCGGGA A C MAP3K10 Ensembl:ENSG00000130758 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr19:40191501..40191675;chr19:40191494..40191754 26863410 MeRIP-seq:(Medium) rs934390273 Functional Loss SNV dbSNP153 33..33 33 - - - 84383 RMVar_ID_84383 Human_SNP_ID_665736644 m1A Human chr19 - 40191807 40191807 40191807 TTGGCTGTACGGGCGGGGCGGGGCGGGGTGGGAGTGGGGCGGCAGGTTCACCCGTGCCCCCCAAA TTGGCTGTACGGGCGGGGCGGGGCGGGGTGGGGGTGGGGCGGCAGGTTCACCCGTGCCCCCCAAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:40191690..40191822 26863196 MeRIP-seq:(Medium) rs911562422 Functional Loss SNV dbSNP153 33..33 33 - - - 84384 RMVar_ID_84384 Human_SNP_ID_665736669 m1A Human chr19 + 40191853 40191853 40191853 GCCCCGCCCGTACAGCCAAATCGGAAGGGACGAGCCTGCCCTTTGAAAGGGTTTTTTTTCTTGCT GCCCCGCCCGTACAGCCAAATCGGAAGGGACGCGCCTGCCCTTTGAAAGGGTTTTTTTTCTTGCT A C MAP3K10 Ensembl:ENSG00000130758 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40191690..40191863 32194978 MeRIP-seq:(Medium) rs1028050294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82002,RMVar_hsa_circ_194828 84385 RMVar_ID_84385 Human_SNP_ID_665736708 m1A Human chr19 + 40192000 40192000 40192000 CGCCCTCTGCATCCCGCGGGCAGCCTGTGTGAAGCGGCCTCCCGCAGCCCCCGGCCCCTCCCCCA CGCCCTCTGCATCCCGCGGGCAGCCTGTGTGAGGCGGCCTCCCGCAGCCCCCGGCCCCTCCCCCA A G MAP3K10 Ensembl:ENSG00000130758 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40191955..40192020 26863196 MeRIP-seq:(Medium) rs1297521660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82002,RMVar_hsa_circ_194828 84386 RMVar_ID_84386 Human_SNP_ID_665739570 m1A Human chr19 + 40203921 40203921 40203921 TTACACAAGGGAAGAGTGTTCTCCACAAAGGGAACAGCATGTGTGAAGGCCAGAGGTTAGAAAGC TTACACAAGGGAAGAGTGTTCTCCACAAAGGGGACAGCATGTGTGAAGGCCAGAGGTTAGAAAGC A G MAP3K10 Ensembl:ENSG00000130758 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40203915..40204063 26863196 MeRIP-seq:(Medium) rs1447514732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117982,RMVar_hsa_circ_194829 84387 RMVar_ID_84387 Human_SNP_ID_665740078 m1A Human chr19 + 40205990 40205990 40205990 GCGCTTCCAGGAGGAGCAGCTGCGGCGGCGGGAGCAGGAGCTGGCAGAACGTGAGATGGACATCG GCGCTTCCAGGAGGAGCAGCTGCGGCGGCGGGGGCAGGAGCTGGCAGAACGTGAGATGGACATCG A G MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40205945..40206025 26863196 MeRIP-seq:(Medium) rs1221522549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18997833 Human_Splice_Rec_2007302,Human_Splice_Rec_2007322,Human_Splice_Rec_2007348,Human_Splice_Rec_2007350 RMVar_hsa_circ_117982,RMVar_hsa_circ_127469,RMVar_hsa_circ_194829,RMVar_hsa_circ_338457,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831,RMVar_hsa_circ_377282 84388 RMVar_ID_84388 Human_SNP_ID_665740086 m1A Human chr19 + 40206017 40206017 40206017 GCGGGAGCAGGAGCTGGCAGAACGTGAGATGGACATCGTGGAACGGGAGCTGCACCTGCTCATGT GCGGGAGCAGGAGCTGGCAGAACGTGAGATGGGCATCGTGGAACGGGAGCTGCACCTGCTCATGT A G MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40205966..40206052 26863196 MeRIP-seq:(Medium) rs1347852085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825697,Human_RBP_ID_1888064 Human_miRNA_ID_2014006 RMVar_hsa_circ_117982,RMVar_hsa_circ_127469,RMVar_hsa_circ_194829,RMVar_hsa_circ_338457,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831,RMVar_hsa_circ_377282 84389 RMVar_ID_84389 Human_SNP_ID_665741989 m1A Human chr19 - 40212898 40212898 40212898 CCCACGTTCGTCCCTTCTTCTTGCCCCCGACCAGTTCTTCCTTCTTTGGGGGCCCACCGCGGCTC CCCACGTTCGTCCCTTCTTCTTGCCCCCGACCCGTTCTTCCTTCTTTGGGGGCCCACCGCGGCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40212847..40213153 26863196 MeRIP-seq:(Medium) rs1458756531 Functional Loss SNV dbSNP153 33..33 33 - - - 84390 RMVar_ID_84390 Human_SNP_ID_665742073 m1A Human chr19 + 40213101 40213101 40213101 CCCGCAGGCTGAAGGGGCTGGGGGAAGGAAGCAAACAGTGGTCATCAAGTGCCCCCAACCTGGGC CCCGCAGGCTGAAGGGGCTGGGGGAAGGAAGCCAACAGTGGTCATCAAGTGCCCCCAACCTGGGC A C MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40212820..40213172 26863196 MeRIP-seq:(Medium) rs1357294830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18733042 Human_Splice_Rec_2007308,Human_Splice_Rec_2007309,Human_Splice_Rec_2007332,Human_Splice_Rec_2007342,Human_Splice_Rec_2007343,Human_Splice_Rec_2007354 Human_miRNA_ID_1343908,Human_miRNA_ID_2648654,Human_miRNA_ID_2671250,Human_miRNA_ID_3101901 RMVar_hsa_circ_49061,RMVar_hsa_circ_127469,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831 84391 RMVar_ID_84391 Human_SNP_ID_665742143 m1A Human chr19 - 40213273 40213273 40213273 CCCAGGAAGGCCTTCCACTCACTGGCCCAGTGAAACCTGGTCTCTTCGCTCAGCCCCAGGAGGCT CCCAGGAAGGCCTTCCACTCACTGGCCCAGTGGAACCTGGTCTCTTCGCTCAGCCCCAGGAGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40213229..40213311 26863196 MeRIP-seq:(Medium) rs1443244344 Functional Loss SNV dbSNP153 33..33 33 - - - 84392 RMVar_ID_84392 Human_SNP_ID_665742511 m1A Human chr19 + 40214054 40214054 40214054 CGCGCCCACACCCACGCCCTCGCCCAGCACCAACCCCCTGGTGGACCTGGAGCTGGAGAGCTTCA CGCGCCCACACCCACGCCCTCGCCCAGCACCACCCCCCTGGTGGACCTGGAGCTGGAGAGCTTCA A C MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40213889..40214164 26863196 MeRIP-seq:(Medium) rs538403826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522013 RMVar_hsa_circ_127469,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831 84393 RMVar_ID_84393 Human_SNP_ID_665742535 m1A Human chr19 + 40214110 40214110 40214110 AGAGCTTCAAGAAGGACCCCCGCCAGTCGCTCACGCCCACCCACGTCACGGCTGCATGCGCTGTG AGAGCTTCAAGAAGGACCCCCGCCAGTCGCTCGCGCCCACCCACGTCACGGCTGCATGCGCTGTG A G MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40214062..40214204 26863196 MeRIP-seq:(Medium) rs1338533135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1373407,Human_RBP_ID_17925260 RMVar_hsa_circ_127469,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831 84394 RMVar_ID_84394 Human_SNP_ID_665748085 m1A Human chr19 - 40232051 40232049 40232051 CTCCAGGCCCTCAGTGCTGCTTAGGCTAAGAGAGGTGGGGTGGAGGGACAGGGCTGGAAGATCTG CTCCAGGCCCTCAGTGCTGCTTAGGCTAAGAG__GTGGGGTGGAGGGACAGGGCTGGAAGATCTG CCT C AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40232004..40232115 26863196 MeRIP-seq:(Medium) rs1015020094 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7695,Human_RBP_ID_3586393,Human_RBP_ID_6763999,Human_RBP_ID_8102980,Human_RBP_ID_8233147,Human_RBP_ID_13457010,Human_RBP_ID_21977964,Human_RBP_ID_23797800 84395 RMVar_ID_84395 Human_SNP_ID_665748289 m1A Human chr19 - 40232751 40232751 40232751 CGTGCCTCGGACTGCGTGTGTCGGCGGGACGCAGGCACACGTGGGTGTGTGTGCATGTGTGTTTG CGTGCCTCGGACTGCGTGTGTCGGCGGGACGCTGGCACACGTGGGTGTGTGTGCATGTGTGTTTG T A AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40232711..40232840 26863196 MeRIP-seq:(Medium) rs999658585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241314,Human_RBP_ID_522061,Human_RBP_ID_5292816,Human_RBP_ID_17925289,Human_RBP_ID_23797813 84396 RMVar_ID_84396 Human_SNP_ID_665748290 m1A Human chr19 - 40232751 40232751 40232751 CGTGCCTCGGACTGCGTGTGTCGGCGGGACGCAGGCACACGTGGGTGTGTGTGCATGTGTGTTTG CGTGCCTCGGACTGCGTGTGTCGGCGGGACGCGGGCACACGTGGGTGTGTGTGCATGTGTGTTTG T C AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40232711..40232840 26863196 MeRIP-seq:(Medium) rs999658585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241314,Human_RBP_ID_522061,Human_RBP_ID_5292816,Human_RBP_ID_17925289,Human_RBP_ID_23797813 84397 RMVar_ID_84397 Human_SNP_ID_665748621 m1A Human chr19 - 40233684 40233678 40233685 AGCGGCCCCTGCAGCCCCTGCCTCCAGCCTCCAGCCTCACCTTTGTGCCCAGACTCGCATTTGGA AGCGGCCCCTGCAGCCCCTGCCTCCAGCCTC_______ACCTTTGTGCCCAGACTCGCATTTGGA TGAGGCTG T AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:40233635..40233848;chr19:40233635..40233719 26863196 MeRIP-seq:(Medium) rs756792297 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_522079,Human_RBP_ID_1373415,Human_RBP_ID_17925303,Human_RBP_ID_18733087,Human_RBP_ID_22972924,Human_RBP_ID_26474986 Human_miRNA_ID_172698 84398 RMVar_ID_84398 Human_SNP_ID_665748624 m1A Human chr19 - 40233684 40233684 40233684 AGCGGCCCCTGCAGCCCCTGCCTCCAGCCTCCAGCCTCACCTTTGTGCCCAGACTCGCATTTGGA AGCGGCCCCTGCAGCCCCTGCCTCCAGCCTCCGGCCTCACCTTTGTGCCCAGACTCGCATTTGGA T C AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:40233635..40233848;chr19:40233635..40233719 26863196 MeRIP-seq:(Medium) rs1300271878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522079,Human_RBP_ID_1373415,Human_RBP_ID_17925303,Human_RBP_ID_18733087,Human_RBP_ID_22972924,Human_RBP_ID_26474986 Human_miRNA_ID_172698 84399 RMVar_ID_84399 Human_SNP_ID_665748644 m1A Human chr19 - 40233716 40233716 40233716 GTTCTTCTTCAGGCCCCTCCCAGACGCACCCCAGCGGCCCCTGCAGCCCCTGCCTCCAGCCTCCA GTTCTTCTTCAGGCCCCTCCCAGACGCACCCCTGCGGCCCCTGCAGCCCCTGCCTCCAGCCTCCA T A AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40233433..40233902 26863196 MeRIP-seq:(Medium) rs1484456059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241315,Human_RBP_ID_4529175,Human_RBP_ID_5116890,Human_RBP_ID_18946857,Human_RBP_ID_22502943,Human_RBP_ID_24485481 Human_miRNA_ID_1358189 84400 RMVar_ID_84400 Human_SNP_ID_665749539 m1A Human chr19 + 40236401 40236401 40236401 AGCATGAGGTTTTCCAGCTGTTGGAAAAGTCAACGGATCTCAGGTGCATGCTCCCAAGGCTTCCT AGCATGAGGTTTTCCAGCTGTTGGAAAAGTCAGCGGATCTCAGGTGCATGCTCCCAAGGCTTCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40236395..40236595 32194978 MeRIP-seq:(Medium) rs1053438779 Functional Loss SNV dbSNP153 33..33 33 - - - 84401 RMVar_ID_84401 Human_SNP_ID_665750546 m1A Human chr19 - 40240095 40240095 40240095 CCGCAGTCTGTCTGCAGGATGAAGTCGCTCACACAGTCACCGAGAGCCGGGTCCTCCAGAACACC CCGCAGTCTGTCTGCAGGATGAAGTCGCTCACGCAGTCACCGAGAGCCGGGTCCTCCAGAACACC T C AKT2 Ensembl:ENSG00000105221 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40239994..40240095 32194978 MeRIP-seq:(Medium) rs1568526119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565704,Human_RBP_ID_3955043,Human_RBP_ID_13457164,Human_RBP_ID_18997847,Human_RBP_ID_19090179,Human_RBP_ID_22546050,Human_RBP_ID_22665451 Human_Splice_Rec_2007404,Human_Splice_Rec_2007405,Human_Splice_Rec_2007430,Human_Splice_Rec_2007431,Human_Splice_Rec_2007456,Human_Splice_Rec_2007457,Human_Splice_Rec_2007486,Human_Splice_Rec_2007487,Human_Splice_Rec_2007526,Human_Splice_Rec_2007527,Human_Splice_Rec_2007550,Human_Splice_Rec_2007551,Human_Splice_Rec_2007580,Human_Splice_Rec_2007581,Human_Splice_Rec_2007612,Human_Splice_Rec_2007613,Human_Splice_Rec_2007635,Human_Splice_Rec_2007656,Human_Splice_Rec_2007657,Human_Splice_Rec_2007670,Human_Splice_Rec_2007671,Human_Splice_Rec_2007684,Human_Splice_Rec_2007692 Human_miRNA_ID_2038004,Human_miRNA_ID_2348704,Human_miRNA_ID_3115294 RMVar_hsa_circ_2264,RMVar_hsa_circ_112632,RMVar_hsa_circ_96737,RMVar_hsa_circ_369843,RMVar_hsa_circ_194833,RMVar_hsa_circ_194834,RMVar_hsa_circ_194835,RMVar_hsa_circ_324315,RMVar_hsa_circ_372277,RMVar_hsa_circ_282994,RMVar_hsa_circ_62426,RMVar_hsa_circ_194837,RMVar_hsa_circ_194838,RMVar_hsa_circ_194839,RMVar_hsa_circ_100928,RMVar_hsa_circ_77340,RMVar_hsa_circ_194840,RMVar_hsa_circ_106401,RMVar_hsa_circ_194841,RMVar_hsa_circ_194842 84402 RMVar_ID_84402 Human_SNP_ID_665751226 m1A Human chr19 - 40242574 40242574 40242574 GTGTGGCTCCCCCAGTGACTCCTCCACGACTGAGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG GTGTGGCTCCCCCAGTGACTCCTCCACGACTGTGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG T A AKT2 Ensembl:ENSG00000105221 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40242473..40242574 32194978 MeRIP-seq:(Medium) rs1028818887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239645,Human_RBP_ID_3955044,Human_RBP_ID_9346745,Human_RBP_ID_18733132,Human_RBP_ID_18994984,Human_RBP_ID_22977760,Human_RBP_ID_26336304,Human_RBP_ID_26770045,Human_RBP_ID_27815446 Human_Splice_Rec_2007401,Human_Splice_Rec_2007427,Human_Splice_Rec_2007453,Human_Splice_Rec_2007483,Human_Splice_Rec_2007523,Human_Splice_Rec_2007547,Human_Splice_Rec_2007577,Human_Splice_Rec_2007597,Human_Splice_Rec_2007653,Human_Splice_Rec_2007667,Human_Splice_Rec_2007681,Human_Splice_Rec_2007689,Human_Splice_Rec_2007699,Human_Splice_Rec_2007709,Human_Splice_Rec_2007717,Human_Splice_Rec_2007727,Human_Splice_Rec_2007735 RMVar_hsa_circ_2264,RMVar_hsa_circ_112632,RMVar_hsa_circ_369843,RMVar_hsa_circ_194834,RMVar_hsa_circ_194835,RMVar_hsa_circ_324315,RMVar_hsa_circ_372277,RMVar_hsa_circ_194838,RMVar_hsa_circ_194839,RMVar_hsa_circ_100928,RMVar_hsa_circ_77340,RMVar_hsa_circ_194840,RMVar_hsa_circ_194841,RMVar_hsa_circ_194843,RMVar_hsa_circ_291433,RMVar_hsa_circ_291922,RMVar_hsa_circ_126465,RMVar_hsa_circ_194844,RMVar_hsa_circ_194845 84403 RMVar_ID_84403 Human_SNP_ID_665751227 m1A Human chr19 - 40242574 40242574 40242574 GTGTGGCTCCCCCAGTGACTCCTCCACGACTGAGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG GTGTGGCTCCCCCAGTGACTCCTCCACGACTGCGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG T G AKT2 Ensembl:ENSG00000105221 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40242473..40242574 32194978 MeRIP-seq:(Medium) rs1028818887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239645,Human_RBP_ID_3955044,Human_RBP_ID_9346745,Human_RBP_ID_18733132,Human_RBP_ID_18994984,Human_RBP_ID_22977760,Human_RBP_ID_26336304,Human_RBP_ID_26770045,Human_RBP_ID_27815446 Human_Splice_Rec_2007401,Human_Splice_Rec_2007427,Human_Splice_Rec_2007453,Human_Splice_Rec_2007483,Human_Splice_Rec_2007523,Human_Splice_Rec_2007547,Human_Splice_Rec_2007577,Human_Splice_Rec_2007597,Human_Splice_Rec_2007653,Human_Splice_Rec_2007667,Human_Splice_Rec_2007681,Human_Splice_Rec_2007689,Human_Splice_Rec_2007699,Human_Splice_Rec_2007709,Human_Splice_Rec_2007717,Human_Splice_Rec_2007727,Human_Splice_Rec_2007735 RMVar_hsa_circ_2264,RMVar_hsa_circ_112632,RMVar_hsa_circ_369843,RMVar_hsa_circ_194834,RMVar_hsa_circ_194835,RMVar_hsa_circ_324315,RMVar_hsa_circ_372277,RMVar_hsa_circ_194838,RMVar_hsa_circ_194839,RMVar_hsa_circ_100928,RMVar_hsa_circ_77340,RMVar_hsa_circ_194840,RMVar_hsa_circ_194841,RMVar_hsa_circ_194843,RMVar_hsa_circ_291433,RMVar_hsa_circ_291922,RMVar_hsa_circ_126465,RMVar_hsa_circ_194844,RMVar_hsa_circ_194845 84404 RMVar_ID_84404 Human_SNP_ID_665753073 m1A Human chr19 + 40250064 40250063 40250064 ATGTTTAAGGAACAGCAAGGAGACACGTGGCTAAGTGAGGGTGCTTGTGGTAGGAAATGCTTCTG ATGTTTAAGGAACAGCAAGGAGACACGTGGCT_AGTGAGGGTGCTTGTGGTAGGAAATGCTTCTG TA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40250062..40250159 26863196 MeRIP-seq:(Medium) rs1254573901 Functional Loss DEL dbSNP153 33..33 33 - - - 84405 RMVar_ID_84405 Human_SNP_ID_665756831 m1A Human chr19 + 40264556 40264556 40264556 CTCCCCCAGCTCGCCCTAGCTCACACTGCTCCAGCCACGCTGTTACCAGAAAACACCAGGCACAT CTCCCCCAGCTCGCCCTAGCTCACACTGCTCCGGCCACGCTGTTACCAGAAAACACCAGGCACAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40264551..40264708 26863196 MeRIP-seq:(Medium) rs907913517 Functional Loss SNV dbSNP153 33..33 33 - - - 84406 RMVar_ID_84406 Human_SNP_ID_665757442 m1A Human chr19 - 40267007 40267007 40267007 GGGAGAGATGGTCACGTTAGAGGTTGACACACAGAACAGTGGGAGATACAGAAATACATACATAT GGGAGAGATGGTCACGTTAGAGGTTGACACACGGAACAGTGGGAGATACAGAAATACATACATAT T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40267005..40267533 26863196 MeRIP-seq:(Medium) rs1031690321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9425332 RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 84407 RMVar_ID_84407 Human_SNP_ID_665757525 m1A Human chr19 - 40267366 40267366 40267366 ATGGAGAGTCAGGTAGGGCGGAGAGGCTGGAGAGGTGCAATAGTCAACGTCATGGTCCTTAGCCT ATGGAGAGTCAGGTAGGGCGGAGAGGCTGGAGGGGTGCAATAGTCAACGTCATGGTCCTTAGCCT T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40267362..40267536 26863196 MeRIP-seq:(Medium) rs1225853700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9922248 RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 84408 RMVar_ID_84408 Human_SNP_ID_665760337 m1A Human chr19 - 40277467 40277467 40277467 GACACAGGTGGGTGGGGAGGGACCTGTGTGGGAGAGAGCTGGCTGGATTCAGGTGGCAGCCAGGG GACACAGGTGGGTGGGGAGGGACCTGTGTGGGGGAGAGCTGGCTGGATTCAGGTGGCAGCCAGGG T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40277465..40277811 26863196 MeRIP-seq:(Medium) rs904864759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825627,Human_RBP_ID_3583633,Human_RBP_ID_4529350,Human_RBP_ID_5145759,Human_RBP_ID_6764310,Human_RBP_ID_8100621,Human_RBP_ID_9426163,Human_RBP_ID_17207562,Human_RBP_ID_18421381 RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 84409 RMVar_ID_84409 Human_SNP_ID_665760369 m1A Human chr19 - 40277603 40277603 40277603 ATATCTGGATGTGCTGGTGGAACAGCAGGCCCATGTAGCTGGAGCCGGGGGAGTGGGTGAGGGGG ATATCTGGATGTGCTGGTGGAACAGCAGGCCCGTGTAGCTGGAGCCGGGGGAGTGGGTGAGGGGG T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:40277503..40277798 26863196 MeRIP-seq:(Medium) rs890753209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23797997 RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 84410 RMVar_ID_84410 Human_SNP_ID_665761147 m1A Human chr19 + 40280616 40280616 40280616 CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCAGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCCGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40280613..40280801 26863196 MeRIP-seq:(Medium) rs8102171 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10097,GWAS_ID_10098,GWAS_ID_10099,GWAS_ID_10100,GWAS_ID_10101,GWAS_ID_10102,GWAS_ID_10103,GWAS_ID_10104,GWAS_ID_10105,GWAS_ID_10106,GWAS_ID_10107,GWAS_ID_10108,GWAS_ID_10109,GWAS_ID_10110 84411 RMVar_ID_84411 Human_SNP_ID_665761148 m1A Human chr19 + 40280616 40280616 40280616 CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCAGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCTGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40280613..40280801 26863196 MeRIP-seq:(Medium) rs8102171 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10097,GWAS_ID_10098,GWAS_ID_10099,GWAS_ID_10100,GWAS_ID_10101,GWAS_ID_10102,GWAS_ID_10103,GWAS_ID_10104,GWAS_ID_10105,GWAS_ID_10106,GWAS_ID_10107,GWAS_ID_10108,GWAS_ID_10109,GWAS_ID_10110 84412 RMVar_ID_84412 Human_SNP_ID_665761168 m1A Human chr19 + 40280720 40280720 40280720 CACCAAGCTCTGTCCTCCCTTCAGACCTTTGCACTGTGGTTCCCTCCACCTGGAGGGCTGTTCCT CACCAAGCTCTGTCCTCCCTTCAGACCTTTGCGCTGTGGTTCCCTCCACCTGGAGGGCTGTTCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40280684..40280814 26863196 MeRIP-seq:(Medium) rs1040736351 Functional Loss SNV dbSNP153 33..33 33 - - - 84413 RMVar_ID_84413 Human_SNP_ID_665761537 m1A Human chr19 - 40282243 40282243 40282243 GTTGTGAGGATTAAATGAATTAATCCACGAGAAGCTCCTAGAATGGTGCCTGGTACTGTGTAAGT GTTGTGAGGATTAAATGAATTAATCCACGAGATGCTCCTAGAATGGTGCCTGGTACTGTGTAAGT T A AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40282240..40282441 32194978 MeRIP-seq:(Medium) rs1377725277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565757,Human_RBP_ID_1888156,Human_RBP_ID_6764389,Human_RBP_ID_13457835,Human_RBP_ID_23798030 Human_Splice_Rec_2007783,Human_Splice_Rec_2007800,Human_Splice_Rec_2007801 RMVar_hsa_circ_23550 84414 RMVar_ID_84414 Human_SNP_ID_665762035 m1A Human chr19 + 40284137 40284137 40284137 GTTACTCCAGCCCAGGCGTCTTGCTGAGCCCCAAGAGGTCTCCAAATGAGAGGAAGAGGTCCTCA GTTACTCCAGCCCAGGCGTCTTGCTGAGCCCCTAGAGGTCTCCAAATGAGAGGAAGAGGTCCTCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40284132..40284234 32194978 MeRIP-seq:(Medium) rs554916649 Functional Loss SNV dbSNP153 33..33 33 - - - 84415 RMVar_ID_84415 Human_SNP_ID_665762133 m1A Human chr19 + 40284495 40284495 40284495 TGACGTTCCCTCCAGAGTCGTTAAGAAGTTCAATAAAGGCTGAGATCAGTGTAAACCCCCAACGC TGACGTTCCCTCCAGAGTCGTTAAGAAGTTCAGTAAAGGCTGAGATCAGTGTAAACCCCCAACGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40284493..40284746 26863196 MeRIP-seq:(Medium) rs1246277060 Functional Loss SNV dbSNP153 33..33 33 - - - 84416 RMVar_ID_84416 Human_SNP_ID_665762135 m1A Human chr19 - 40284503 40284503 40284503 CGTGTGTGGCGTTGGGGGTTTACACTGATCTCAGCCTTTATTGAACTTCTTAACGACTCTGGAGG CGTGTGTGGCGTTGGGGGTTTACACTGATCTCGGCCTTTATTGAACTTCTTAACGACTCTGGAGG T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40284501..40285008 26863196 MeRIP-seq:(Medium) rs879584869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378,Human_RBP_ID_1094077,Human_RBP_ID_2566039,Human_RBP_ID_3588245,Human_RBP_ID_8103000,Human_RBP_ID_17131922,Human_RBP_ID_18490680,Human_RBP_ID_22973030,Human_RBP_ID_23798044,Human_RBP_ID_26653917,Human_RBP_ID_27680313 84417 RMVar_ID_84417 Human_SNP_ID_665762205 m1A Human chr19 + 40284821 40284821 40284821 GCTTCCACAGCGCCAAAAAGGTACAGCCCTCTACACTTGATGCGGCGCGCCCCCTCGATAGCTTA GCTTCCACAGCGCCAAAAAGGTACAGCCCTCTGCACTTGATGCGGCGCGCCCCCTCGATAGCTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40284817..40285004 26863196 MeRIP-seq:(Medium) rs1199327971 Functional Loss SNV dbSNP153 33..33 33 - - - 84418 RMVar_ID_84418 Human_SNP_ID_665762218 m1A Human chr19 + 40284853 40284853 40284853 ACACTTGATGCGGCGCGCCCCCTCGATAGCTTAGCCCGCGCACGCCAGGCTCGATCTGCCCGCCG ACACTTGATGCGGCGCGCCCCCTCGATAGCTTGGCCCGCGCACGCCAGGCTCGATCTGCCCGCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40284789..40285032 26863196 MeRIP-seq:(Medium) rs1020586134 Functional Loss SNV dbSNP153 33..33 33 - - - 84419 RMVar_ID_84419 Human_SNP_ID_665762389 m1A Human chr19 + 40285290 40285267 40285291 TTGTGTTTCCCGGCAGCGGCAACGGCGCCGGCAGCGGCAGCGGCGGCGGCGACGCCTCCTCCGAG TTGTGTTTCC________________________CGGCAGCGGCGGCGGCGACGCCTCCTCCGAG CCGGCAGCGGCAACGGCGCCGGCAG C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr19:40285266..40285356;chr19:40285262..40285353 26863410 MeRIP-seq:(Medium) rs926671678 Functional Loss DEL dbSNP153 11..34 33 - - - 84420 RMVar_ID_84420 Human_SNP_ID_665762403 m1A Human chr19 + 40285290 40285285 40285291 TTGTGTTTCCCGGCAGCGGCAACGGCGCCGGCAGCGGCAGCGGCGGCGGCGACGCCTCCTCCGAG TTGTGTTTCCCGGCAGCGGCAACGGCGC______CGGCAGCGGCGGCGGCGACGCCTCCTCCGAG CCGGCAG C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr19:40285266..40285356;chr19:40285262..40285353 26863410 MeRIP-seq:(Medium) rs938886418 Functional Loss DEL dbSNP153 29..34 33 - - - 84421 RMVar_ID_84421 Human_SNP_ID_665762408 m1A Human chr19 + 40285296 40285296 40285296 TTCCCGGCAGCGGCAACGGCGCCGGCAGCGGCAGCGGCGGCGGCGACGCCTCCTCCGAGGCAGGC TTCCCGGCAGCGGCAACGGCGCCGGCAGCGGCGGCGGCGGCGGCGACGCCTCCTCCGAGGCAGGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:40285260..40285347 26863410 MeRIP-seq:(Medium) rs948489785 Functional Loss SNV dbSNP153 33..33 33 - - - 84422 RMVar_ID_84422 Human_SNP_ID_665771335 m1A Human chr19 + 40321336 40321336 40321336 GGCCGGAGGTACAGGAGGGTCGGGCAGGACGCAGCGGACAGTCGGGCCTTGCCACGGGGACAGAA GGCCGGAGGTACAGGAGGGTCGGGCAGGACGCCGCGGACAGTCGGGCCTTGCCACGGGGACAGAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40321127..40321478 26863196 MeRIP-seq:(Medium) rs1279898983 Functional Loss SNV dbSNP153 33..33 33 - - - 84423 RMVar_ID_84423 Human_SNP_ID_665772754 m1A Human chr19 + 40326422 40326422 40326422 GGCATGTTGATGACGTACTTCCCCTCCATCTCAGCAGTGACCCGGCGCCGCTTGGCAGGAACAGC GGCATGTTGATGACGTACTTCCCCTCCATCTCCGCAGTGACCCGGCGCCGCTTGGCAGGAACAGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40326344..40332541 32194978 MeRIP-seq:(Medium) rs1440034867 Functional Loss SNV dbSNP153 33..33 33 - - - 84424 RMVar_ID_84424 Human_SNP_ID_665783244 m1A Human chr19 + 40365899 40365899 40365899 CAGAAGCTGGGGCCCACCGGAGGTAGCTGCAGACGCCTGAGAGCGAGGCCGAGGCCCCTCAGGGG CAGAAGCTGGGGCCCACCGGAGGTAGCTGCAGCCGCCTGAGAGCGAGGCCGAGGCCCCTCAGGGG A C PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40365851..40365950 26863196 MeRIP-seq:(Medium) rs924061518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557494 Human_Splice_Rec_2007939,Human_Splice_Rec_2007945,Human_Splice_Rec_2007955,Human_Splice_Rec_2007983,Human_Splice_Rec_2008007,Human_Splice_Rec_2008019,Human_Splice_Rec_2008043,Human_Splice_Rec_2008097,Human_Splice_Rec_2008119 RMVar_hsa_circ_266679 84425 RMVar_ID_84425 Human_SNP_ID_665783403 m1A Human chr19 - 40366464 40366464 40366464 GTTTAGGCTTCATCTTCCCTCAAGGCTGGGGGATACGCAGAGCCCAGGTGAGAAGGTGGGTGTGT GTTTAGGCTTCATCTTCCCTCAAGGCTGGGGGGTACGCAGAGCCCAGGTGAGAAGGTGGGTGTGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40366401..40366525 26863196 MeRIP-seq:(Medium) rs1555794404 Functional Loss SNV dbSNP153 33..33 33 - - - 84426 RMVar_ID_84426 Human_SNP_ID_665783408 m1A Human chr19 + 40366470 40366470 40366470 CCACCTTCTCACCTGGGCTCTGCGTATCCCCCAGCCTTGAGGGAAGATGAAGCCTAAACTGATGT CCACCTTCTCACCTGGGCTCTGCGTATCCCCCGGCCTTGAGGGAAGATGAAGCCTAAACTGATGT A G PLD3 Ensembl:ENSG00000105223 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40366401..40366500 26863196 MeRIP-seq:(Medium) rs1462600962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53199,Human_RBP_ID_770736,Human_RBP_ID_1565809,Human_RBP_ID_4529713,Human_RBP_ID_9293684,Human_RBP_ID_9330047,Human_RBP_ID_18193067,Human_RBP_ID_22446758,Human_RBP_ID_26990312 Human_Splice_Rec_2007932,Human_Splice_Rec_2007933,Human_Splice_Rec_2007940,Human_Splice_Rec_2007946,Human_Splice_Rec_2007947,Human_Splice_Rec_2007956,Human_Splice_Rec_2007957,Human_Splice_Rec_2007960,Human_Splice_Rec_2007961,Human_Splice_Rec_2007984,Human_Splice_Rec_2007985,Human_Splice_Rec_2008008,Human_Splice_Rec_2008010,Human_Splice_Rec_2008011,Human_Splice_Rec_2008020,Human_Splice_Rec_2008021,Human_Splice_Rec_2008044,Human_Splice_Rec_2008045,Human_Splice_Rec_2008052,Human_Splice_Rec_2008053,Human_Splice_Rec_2008076,Human_Splice_Rec_2008077,Human_Splice_Rec_2008084,Human_Splice_Rec_2008085,Human_Splice_Rec_2008098,Human_Splice_Rec_2008099,Human_Splice_Rec_2008120,Human_Splice_Rec_2008121,Human_Splice_Rec_2008126,Human_Splice_Rec_2008127,Human_Splice_Rec_2008135,Human_Splice_Rec_2008137 Human_miRNA_ID_2653699,Human_miRNA_ID_2686252,Human_miRNA_ID_2754897 RMVar_hsa_circ_194854,RMVar_hsa_circ_56363,RMVar_hsa_circ_371584,RMVar_hsa_circ_266679,RMVar_hsa_circ_103537,RMVar_hsa_circ_194855 84427 RMVar_ID_84427 Human_SNP_ID_665783411 m1A Human chr19 - 40366502 40366502 40366502 TGCTGAGCCCCCCAATCCACCTACCTCCTGGTACATCAGTTTAGGCTTCATCTTCCCTCAAGGCT TGCTGAGCCCCCCAATCCACCTACCTCCTGGTTCATCAGTTTAGGCTTCATCTTCCCTCAAGGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:40366401..40366525 26863196 MeRIP-seq:(Medium) rs1419132847 Functional Loss SNV dbSNP153 33..33 33 - - - 84428 RMVar_ID_84428 Human_SNP_ID_665783553 m1A Human chr19 - 40366846 40366846 40366846 GCCCAAAGAGATGCAAGTCGCCGTATTCCCATAGAAACAGCTGAGTCATCAGGGCTCCGAAGCCC GCCCAAAGAGATGCAAGTCGCCGTATTCCCATGGAAACAGCTGAGTCATCAGGGCTCCGAAGCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40366626..40366945 32194978 MeRIP-seq:(Medium) rs1432371577 Functional Loss SNV dbSNP153 33..33 33 - - - 84429 RMVar_ID_84429 Human_SNP_ID_665785710 m1A Human chr19 - 40374632 40374632 40374632 CCTGGCCAACTGCAGCGGCTCCCTATCTCCACACCCAGCAGTACCTGTGAGGGTGGGAGAACTCC CCTGGCCAACTGCAGCGGCTCCCTATCTCCACGCCCAGCAGTACCTGTGAGGGTGGGAGAACTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40374627..40374836 26863196 MeRIP-seq:(Medium) rs750221216 Functional Loss SNV dbSNP153 33..33 33 - - - 84430 RMVar_ID_84430 Human_SNP_ID_665786907 m1A Human chr19 - 40378240 40378240 40378240 GGGCAGACAGAAGCGGGGGCGCGGGGACAGGGACCGTGACCCAGAGCACCTGGGTCCGCGGGGGC GGGCAGACAGAAGCGGGGGCGCGGGGACAGGGGCCGTGACCCAGAGCACCTGGGTCCGCGGGGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:40378195..40378375 26863196 MeRIP-seq:(Medium) rs1303677968 Functional Loss SNV dbSNP153 33..33 33 - - - 84431 RMVar_ID_84431 Human_SNP_ID_665791605 m1A Human chr19 + 40394678 40394678 40394678 CCTCGCCCGCCTGTGCCTCTCGGCTTAGCCCCACGTCCAGCTCAAGCTGGGGCACTGTCACGGTG CCTCGCCCGCCTGTGCCTCTCGGCTTAGCCCCGCGTCCAGCTCAAGCTGGGGCACTGTCACGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40394154..40394867 26863196 MeRIP-seq:(Medium) rs1329396084 Functional Loss SNV dbSNP153 33..33 33 - - - 84432 RMVar_ID_84432 Human_SNP_ID_665791796 m1A Human chr19 - 40395084 40395084 40395084 ATCGTGCCAGCCCGGGGGAAAAGGCTGAGTCCACCGCTGTGCAGCTTAAGATCCCCGAGGTGGAG ATCGTGCCAGCCCGGGGGAAAAGGCTGAGTCCCCCGCTGTGCAGCTTAAGATCCCCGAGGTGGAG T G PRX Ensembl:ENSG00000105227 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40395035..40395267 26863196 MeRIP-seq:(Medium) rs1489716811 Functional Loss SNV dbSNP153 33..33 33 - - - 84433 RMVar_ID_84433 Human_SNP_ID_665794402 m1A Human chr19 - 40401666 40401666 40401666 AACAGACAGCAAAAATGCCCCAAGGTGGGACCATGCCTAGCTTGTGGTAGAAACAGTGAGGAAGC AACAGACAGCAAAAATGCCCCAAGGTGGGACCGTGCCTAGCTTGTGGTAGAAACAGTGAGGAAGC T C PRX Ensembl:ENSG00000105227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40401631..40401728 26863196 MeRIP-seq:(Medium) rs928394881 Functional Loss SNV dbSNP153 33..33 33 - - - 84434 RMVar_ID_84434 Human_SNP_ID_665800835 m1A Human chr19 - 40425447 40425447 40425447 GCCAGAATCCCCGGGGGAAAGCCGGCCTGGGCACCGCTAGGGGGCGCCGGGACCCGGGGGCGGAG GCCAGAATCCCCGGGGGAAAGCCGGCCTGGGCGCCGCTAGGGGGCGCCGGGACCCGGGGGCGGAG T C SERTAD1 Ensembl:ENSG00000197019 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40425444..40425577 26863196 MeRIP-seq:(Medium) rs982027419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105194,RMVar_hsa_circ_194860 84435 RMVar_ID_84435 Human_SNP_ID_665800963 m1A Human chr19 + 40425801 40425801 40425801 GCAGCCCCGGCGGGCACCTGTCGGACCCAGGGATCGAACTCTGTGAAGGACCCGGCCGCTGGTAG GCAGCCCCGGCGGGCACCTGTCGGACCCAGGGTTCGAACTCTGTGAAGGACCCGGCCGCTGGTAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40425798..40425948 26863196 MeRIP-seq:(Medium) rs1201348920 Functional Loss SNV dbSNP153 33..33 33 - - - 84436 RMVar_ID_84436 Human_SNP_ID_665805509 m1A Human chr19 + 40441090 40441090 40441090 AGCCCCTCCCACCCCCTCAAGGTGCAAGAGGCAGAGCCTGGGTTTCTATAGCAACCTGGCAGCAC AGCCCCTCCCACCCCCTCAAGGTGCAAGAGGCGGAGCCTGGGTTTCTATAGCAACCTGGCAGCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:40441040..40441287 32194978 MeRIP-seq:(Medium) rs572125420 Functional Loss SNV dbSNP153 33..33 33 - - - 84437 RMVar_ID_84437 Human_SNP_ID_665806551 m1A Human chr19 + 40444267 40444267 40444267 CGACCACCTCCTGGAACGCCCACAGCGTTGCGACCCGCCAGTGCCAGGACCCACCAGTGACCGGT CGACCACCTCCTGGAACGCCCACAGCGTTGCGCCCCGCCAGTGCCAGGACCCACCAGTGACCGGT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:40444144..40444279 26863196 MeRIP-seq:(Medium) rs915076715 Functional Loss SNV dbSNP153 33..33 33 - - - 84438 RMVar_ID_84438 Human_SNP_ID_665808779 m1A Human chr19 - 40451987 40451987 40451987 GGTAACAGTGGACAGGACCAGGCGGAGTGAGAAGAGGTCAGATTTGGAATTATTGTGATCAGCAG GGTAACAGTGGACAGGACCAGGCGGAGTGAGAGGAGGTCAGATTTGGAATTATTGTGATCAGCAG T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40451982..40452220 26863196 MeRIP-seq:(Medium) rs925374811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_345649 84439 RMVar_ID_84439 Human_SNP_ID_665810478 m1A Human chr19 + 40458530 40458530 40458530 CTGATGGCAGCCTGGAGGAGTCCCGCACCAGCACTGTCACTTCGTAACCTGTGGGCAAAGAGGAG CTGATGGCAGCCTGGAGGAGTCCCGCACCAGCGCTGTCACTTCGTAACCTGTGGGCAAAGAGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40458344..40458580 26863196 MeRIP-seq:(Medium) rs138251638 Functional Loss SNV dbSNP153 33..33 33 - - - 84440 RMVar_ID_84440 Human_SNP_ID_665811905 m1A Human chr19 - 40463622 40463618 40463623 CTCCAGCCTGGGTGACACAGCAAGATGAAAGGAAAGAAGGAAGGAAGAAAAGGAGGGAGGGATGG CTCCAGCCTGGGTGACACAGCAAGATGAAAG_____AAGGAAGGAAGAAAAGGAGGGAGGGATGG TCTTTC T BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40463620..40463799 26863196 MeRIP-seq:(Medium) rs1240141009 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84441 RMVar_ID_84441 Human_SNP_ID_665812425 m1A Human chr19 + 40465561 40465561 40465561 CCTCGGCCCGACCCCATGGTGCCCCTTCCTAAAGTTCTGCCCGTCTGTCCCGTGACATGCCCCGC CCTCGGCCCGACCCCATGGTGCCCCTTCCTAAGGTTCTGCCCGTCTGTCCCGTGACATGCCCCGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:40465555..40465742 26863196 MeRIP-seq:(Medium) rs763813647 Functional Loss SNV dbSNP153 33..33 33 - - - 84442 RMVar_ID_84442 Human_SNP_ID_665812426 m1A Human chr19 + 40465561 40465561 40465561 CCTCGGCCCGACCCCATGGTGCCCCTTCCTAAAGTTCTGCCCGTCTGTCCCGTGACATGCCCCGC CCTCGGCCCGACCCCATGGTGCCCCTTCCTAATGTTCTGCCCGTCTGTCCCGTGACATGCCCCGC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:40465555..40465742 26863196 MeRIP-seq:(Medium) rs763813647 Functional Loss SNV dbSNP153 33..33 33 - - - 84443 RMVar_ID_84443 Human_SNP_ID_665812461 m1A Human chr19 - 40465611 40465611 40465611 GGGCTCACCACCCTGGCGCAGGCGGTGCAAGCAGGCATGAGCCGGGGCGGGCGGGGCATGTCACG GGGCTCACCACCCTGGCGCAGGCGGTGCAAGCGGGCATGAGCCGGGGCGGGCGGGGCATGTCACG T C BLVRB Ensembl:ENSG00000090013 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:40465599..40465775 26863196 MeRIP-seq:(Medium) rs778304380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558464,Human_RBP_ID_5320390 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84444 RMVar_ID_84444 Human_SNP_ID_665812467 m1A Human chr19 - 40465624 40465624 40465624 CACTGGCCAGACCGGGCTCACCACCCTGGCGCAGGCGGTGCAAGCAGGCATGAGCCGGGGCGGGC CACTGGCCAGACCGGGCTCACCACCCTGGCGCTGGCGGTGCAAGCAGGCATGAGCCGGGGCGGGC T A BLVRB Ensembl:ENSG00000090013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40458401..40465775 26863196 MeRIP-seq:(Medium) rs148777635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824237,Human_RBP_ID_4558464,Human_RBP_ID_5320390,Human_RBP_ID_22446773 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84445 RMVar_ID_84445 Human_SNP_ID_665812468 m1A Human chr19 - 40465624 40465624 40465624 CACTGGCCAGACCGGGCTCACCACCCTGGCGCAGGCGGTGCAAGCAGGCATGAGCCGGGGCGGGC CACTGGCCAGACCGGGCTCACCACCCTGGCGCGGGCGGTGCAAGCAGGCATGAGCCGGGGCGGGC T C BLVRB Ensembl:ENSG00000090013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40458401..40465775 26863196 MeRIP-seq:(Medium) rs148777635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824237,Human_RBP_ID_4558464,Human_RBP_ID_5320390,Human_RBP_ID_22446773 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84446 RMVar_ID_84446 Human_SNP_ID_665812498 m1A Human chr19 - 40465673 40465673 40465673 CCCCACGATCCCGTACGATGGCCGTCAAGAAGATCGCGATCTTCGGCGCCACTGGCCAGACCGGG CCCCACGATCCCGTACGATGGCCGTCAAGAAGGTCGCGATCTTCGGCGCCACTGGCCAGACCGGG T C BLVRB Ensembl:ENSG00000090013 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:40458432..40465791 26863410 MeRIP-seq:(Medium) rs753037038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4529993,Human_RBP_ID_5320390,Human_RBP_ID_22449483,Human_RBP_ID_22533167,Human_RBP_ID_23798165 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84447 RMVar_ID_84447 Human_SNP_ID_665812524 m1A Human chr19 - 40465716 40465716 40465716 GCCAGTGGGTTCCCGCGCGTGCCGAGACTCTGAGGCCTTGCACCCCCACGATCCCGTACGATGGC GCCAGTGGGTTCCCGCGCGTGCCGAGACTCTGTGGCCTTGCACCCCCACGATCCCGTACGATGGC T A BLVRB Ensembl:ENSG00000090013 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40465406..40465775 26863196 MeRIP-seq:(Medium) rs901064225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770296,Human_RBP_ID_4529998,Human_RBP_ID_5320390,Human_RBP_ID_9328943,Human_RBP_ID_22446774 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84448 RMVar_ID_84448 Human_SNP_ID_665812525 m1A Human chr19 - 40465716 40465716 40465716 GCCAGTGGGTTCCCGCGCGTGCCGAGACTCTGAGGCCTTGCACCCCCACGATCCCGTACGATGGC GCCAGTGGGTTCCCGCGCGTGCCGAGACTCTGGGGCCTTGCACCCCCACGATCCCGTACGATGGC T C BLVRB Ensembl:ENSG00000090013 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40465406..40465775 26863196 MeRIP-seq:(Medium) rs901064225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770296,Human_RBP_ID_4529998,Human_RBP_ID_5320390,Human_RBP_ID_9328943,Human_RBP_ID_22446774 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 84449 RMVar_ID_84449 Human_SNP_ID_665841858 m1A Human chr19 - 40576962 40576962 40576962 CACACTCACCTCTTGCCTCCCACATTCAGATGAATGACTTCCCCGGGAGGCCCCCGACTGGGGAC CACACTCACCTCTTGCCTCCCACATTCAGATGGATGACTTCCCCGGGAGGCCCCCGACTGGGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40576912..40577014 26863196 MeRIP-seq:(Medium) rs16974365 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_10111 84450 RMVar_ID_84450 Human_SNP_ID_665843650 m1A Human chr19 - 40582626 40582626 40582626 CCTCCTCCAGGAAGGCTTCCCTGGTGCTCCTTAGGCCTTTATCACAGACATCCCCAGGCTCTGGC CCTCCTCCAGGAAGGCTTCCCTGGTGCTCCTTGGGCCTTTATCACAGACATCCCCAGGCTCTGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40582621..40582940 26863196 MeRIP-seq:(Medium) rs138004365 Functional Loss SNV dbSNP153 33..33 33 - - - 84451 RMVar_ID_84451 Human_SNP_ID_665846133 m1A Human chr19 + 40591129 40591129 40591129 CGGAGTGGGCCAGACCTCCGACGGCCACCCACACCAGCCCCGTGGCCCTCCAGCGGTCTCGGCAC CGGAGTGGGCCAGACCTCCGACGGCCACCCACCCCAGCCCCGTGGCCCTCCAGCGGTCTCGGCAC A C SHKBP1 Ensembl:ENSG00000160410 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40591079..40591178 26863196 MeRIP-seq:(Medium) rs373745964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387366,Human_RBP_ID_17656143 RMVar_hsa_circ_94986,RMVar_hsa_circ_92136,RMVar_hsa_circ_88101,RMVar_hsa_circ_112407,RMVar_hsa_circ_105436,RMVar_hsa_circ_194877,RMVar_hsa_circ_194878,RMVar_hsa_circ_194882,RMVar_hsa_circ_83542,RMVar_hsa_circ_194885,RMVar_hsa_circ_194889,RMVar_hsa_circ_95192,RMVar_hsa_circ_194890,RMVar_hsa_circ_194891,RMVar_hsa_circ_83815,RMVar_hsa_circ_194892,RMVar_hsa_circ_194893 84452 RMVar_ID_84452 Human_SNP_ID_665846134 m1A Human chr19 + 40591129 40591129 40591129 CGGAGTGGGCCAGACCTCCGACGGCCACCCACACCAGCCCCGTGGCCCTCCAGCGGTCTCGGCAC CGGAGTGGGCCAGACCTCCGACGGCCACCCACGCCAGCCCCGTGGCCCTCCAGCGGTCTCGGCAC A G SHKBP1 Ensembl:ENSG00000160410 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40591079..40591178 26863196 MeRIP-seq:(Medium) rs373745964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387366,Human_RBP_ID_17656143 RMVar_hsa_circ_94986,RMVar_hsa_circ_92136,RMVar_hsa_circ_88101,RMVar_hsa_circ_112407,RMVar_hsa_circ_105436,RMVar_hsa_circ_194877,RMVar_hsa_circ_194878,RMVar_hsa_circ_194882,RMVar_hsa_circ_83542,RMVar_hsa_circ_194885,RMVar_hsa_circ_194889,RMVar_hsa_circ_95192,RMVar_hsa_circ_194890,RMVar_hsa_circ_194891,RMVar_hsa_circ_83815,RMVar_hsa_circ_194892,RMVar_hsa_circ_194893 84453 RMVar_ID_84453 Human_SNP_ID_665847773 m1A Human chr19 + 40597250 40597250 40597250 ACTCGGCGCCCGACACGATGCCGAGGCCTGGCACCAGCGGCCGCCGCCCCCTCCTGCTGGTGCTG ACTCGGCGCCCGACACGATGCCGAGGCCTGGCGCCAGCGGCCGCCGCCCCCTCCTGCTGGTGCTG A G LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40597201..40597393 26863196 MeRIP-seq:(Medium) rs1568399241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558473 Human_miRNA_ID_2052772,Human_miRNA_ID_2387422,Human_miRNA_ID_2388894,Human_miRNA_ID_3031103 RMVar_hsa_circ_116068,RMVar_hsa_circ_194894 84454 RMVar_ID_84454 Human_SNP_ID_665847785 m1A Human chr19 - 40597278 40597278 40597278 AGGTGGCGGCTGCGAAGAGCGGCAGCAACAGCACCAGCAGGAGGGGGCGGCGGCCGCTGGTGCCA AGGTGGCGGCTGCGAAGAGCGGCAGCAACAGCGCCAGCAGGAGGGGGCGGCGGCCGCTGGTGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40597228..40597386 26863196 MeRIP-seq:(Medium) rs1190392252 Functional Loss SNV dbSNP153 33..33 33 - - - 84455 RMVar_ID_84455 Human_SNP_ID_665847788 m1A Human chr19 - 40597284 40597284 40597284 CGGCGGAGGTGGCGGCTGCGAAGAGCGGCAGCAACAGCACCAGCAGGAGGGGGCGGCGGCCGCTG CGGCGGAGGTGGCGGCTGCGAAGAGCGGCAGCGACAGCACCAGCAGGAGGGGGCGGCGGCCGCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40597236..40597325 26863196 MeRIP-seq:(Medium) rs1418650138 Functional Loss SNV dbSNP153 33..33 33 - - - 84456 RMVar_ID_84456 Human_SNP_ID_665847828 m1A Human chr19 + 40597379 40597379 40597379 TCGAGGTCCCGGGGGTCCCCAGCCGCCCGGCCAGGTAAGCCCCCTGCTTCCTTGTGCCCCTTCCA TCGAGGTCCCGGGGGTCCCCAGCCGCCCGGCCGGGTAAGCCCCCTGCTTCCTTGTGCCCCTTCCA A G LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40597306..40598550 32194978 MeRIP-seq:(Medium) rs1435107298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2009103 RMVar_hsa_circ_116068,RMVar_hsa_circ_194894 84457 RMVar_ID_84457 Human_SNP_ID_665849007 m1A Human chr19 + 40601556 40601556 40601556 TCCATGGGCCGACCGGCTCCCGCTGTACCCCGACCTGCGCGCCCCGCAACGCCACCAGCGTGGAC TCCATGGGCCGACCGGCTCCCGCTGTACCCCGGCCTGCGCGCCCCGCAACGCCACCAGCGTGGAC A G LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:40601431..40601637 26863196 MeRIP-seq:(Medium) rs1049456552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4560220 Human_Splice_Rec_2009183 RMVar_hsa_circ_116068,RMVar_hsa_circ_194894 84458 RMVar_ID_84458 Human_SNP_ID_665849920 m1A Human chr19 - 40605121 40605115 40605121 CGGGGGCCGGGCGCCCGAGGAGTGCAACTGGCAGAACTTGCCAGCGAAGTCCGGGGGACAGAGGC CGGGGGCCGGGCGCCCGAGGAGTGCAACTGGC______TGCCAGCGAAGTCCGGGGGACAGAGGC AAGTTCT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40605073..40606276 32194978 MeRIP-seq:(Medium) rs1427367611 Functional Loss DEL dbSNP153 33..38 33 - - - 84459 RMVar_ID_84459 Human_SNP_ID_665849931 m1A Human chr19 - 40605136 40605136 40605136 TGGTACAGCCGGGGCCGGGGGCCGGGCGCCCGAGGAGTGCAACTGGCAGAACTTGCCAGCGAAGT TGGTACAGCCGGGGCCGGGGGCCGGGCGCCCGGGGAGTGCAACTGGCAGAACTTGCCAGCGAAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40605085..40605249 26863196 MeRIP-seq:(Medium) rs1280152516 Functional Loss SNV dbSNP153 33..33 33 - - - 84460 RMVar_ID_84460 Human_SNP_ID_665850064 m1A Human chr19 - 40605508 40605508 40605508 CGCGCCGCCGCTTCCGCCCGCGCCACCGCCTCAGCGTCCGCCTCCTCCCAAGGGCCAGACACACG CGCGCCGCCGCTTCCGCCCGCGCCACCGCCTCGGCGTCCGCCTCCTCCCAAGGGCCAGACACACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40605387..40605625 26863196 MeRIP-seq:(Medium) rs773622227 Functional Loss SNV dbSNP153 33..33 33 - - - 84461 RMVar_ID_84461 Human_SNP_ID_665850934 m1A Human chr19 - 40608031 40608031 40608031 AGAATGTCTTAGAGGCTACAGGTGGGGCCAAGAGCGTTTTCCCACATTTGGGATGGTGGTAGGAA AGAATGTCTTAGAGGCTACAGGTGGGGCCAAGTGCGTTTTCCCACATTTGGGATGGTGGTAGGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40608026..40608113 26863196 MeRIP-seq:(Medium) rs767354968 Functional Loss SNV dbSNP153 33..33 33 - - - 84462 RMVar_ID_84462 Human_SNP_ID_665851047 m1A Human chr19 + 40608339 40608339 40608339 AGCCACCCCGAGTGTCACTCAGCCAGCCTCGTACCCTGCCAGCCACCTCTCGGCCATCTGCAGGT AGCCACCCCGAGTGTCACTCAGCCAGCCTCGTGCCCTGCCAGCCACCTCTCGGCCATCTGCAGGT A G LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40608217..40608396 26863196 MeRIP-seq:(Medium) rs376979408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955072,Human_RBP_ID_22533171 Human_Splice_Rec_2009049,Human_Splice_Rec_2009123,Human_Splice_Rec_2009197,Human_Splice_Rec_2009245 RMVar_hsa_circ_311235,RMVar_hsa_circ_194895 84463 RMVar_ID_84463 Human_SNP_ID_665851144 m1A Human chr19 - 40608533 40608521 40608533 CTGGGCAAGGGAAGCTCAGGGCCGGGCCGGGGATCGGGCCGGGGTTCAGGCCGGGGCTCCAGGCG CTGGGCAAGGGAAGCTCAGGGCCGGGCCGGGG____________TTCAGGCCGGGGCTCCAGGCG ACCCCGGCCCGAT A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:40608325..40608625;chr19:40608454..40608609 26863196 MeRIP-seq:(Medium) rs529188563 Functional Loss DEL dbSNP153 33..44 33 - - - 84464 RMVar_ID_84464 Human_SNP_ID_665851154 m1A Human chr19 - 40608533 40608533 40608533 CTGGGCAAGGGAAGCTCAGGGCCGGGCCGGGGATCGGGCCGGGGTTCAGGCCGGGGCTCCAGGCG CTGGGCAAGGGAAGCTCAGGGCCGGGCCGGGGTTCGGGCCGGGGTTCAGGCCGGGGCTCCAGGCG T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:40608325..40608625;chr19:40608454..40608609 26863196 MeRIP-seq:(Medium) rs537084913 Functional Loss SNV dbSNP153 33..33 33 - - - 84465 RMVar_ID_84465 Human_SNP_ID_665851475 m1A Human chr19 + 40609654 40609654 40609654 TCTGGCTTCCGGCTCAGCCCCCAGGGCACCCGATGCATTGGTGAGCAAGACGGAGGGCGCGGAAG TCTGGCTTCCGGCTCAGCCCCCAGGGCACCCGTTGCATTGGTGAGCAAGACGGAGGGCGCGGAAG A T LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40609526..40610195 32194978 MeRIP-seq:(Medium) rs1203378168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23798224 Human_Splice_Rec_2009053,Human_Splice_Rec_2009127,Human_Splice_Rec_2009201 84466 RMVar_ID_84466 Human_SNP_ID_665851524 m1A Human chr19 - 40609767 40609767 40609767 TCTCGCAGCGCCCGGGAGCACAGGGCGGGGGCACGCGGCGACATTCGTCCACATCTGAGGACACG TCTCGCAGCGCCCGGGAGCACAGGGCGGGGGCGCGCGGCGACATTCGTCCACATCTGAGGACACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40609500..40609850 26863196 MeRIP-seq:(Medium) rs749578668 Functional Loss SNV dbSNP153 33..33 33 - - - 84467 RMVar_ID_84467 Human_SNP_ID_665851709 m1A Human chr19 + 40610241 40610241 40610241 CAACCAATCTCCTGACCGCGACCCCGATTCCAACCCTGCCACACCAGAGCCCTATCCCCAAACTG CAACCAATCTCCTGACCGCGACCCCGATTCCACCCCTGCCACACCAGAGCCCTATCCCCAAACTG A C LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40610203..40610515 26863196 MeRIP-seq:(Medium) rs899257195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082477 84468 RMVar_ID_84468 Human_SNP_ID_665851710 m1A Human chr19 + 40610241 40610241 40610241 CAACCAATCTCCTGACCGCGACCCCGATTCCAACCCTGCCACACCAGAGCCCTATCCCCAAACTG CAACCAATCTCCTGACCGCGACCCCGATTCCAGCCCTGCCACACCAGAGCCCTATCCCCAAACTG A G LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40610203..40610515 26863196 MeRIP-seq:(Medium) rs899257195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17082477 84469 RMVar_ID_84469 Human_SNP_ID_665852271 m1A Human chr19 + 40611956 40611956 40611956 AGCTTCCAGTGTGTCTGCCCCATGGGCTTCCAACCCAACACTGCTGGCTCCGAGTGCGAGGGTGA AGCTTCCAGTGTGTCTGCCCCATGGGCTTCCAGCCCAACACTGCTGGCTCCGAGTGCGAGGGTGA A G LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40611847..40612023 26863196 MeRIP-seq:(Medium) rs1388582769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955081,Human_RBP_ID_8840058,Human_RBP_ID_9293710,Human_RBP_ID_22763392 Human_Splice_Rec_2009060,Human_Splice_Rec_2009061,Human_Splice_Rec_2009134,Human_Splice_Rec_2009135,Human_Splice_Rec_2009176,Human_Splice_Rec_2009177,Human_Splice_Rec_2009208,Human_Splice_Rec_2009209,Human_Splice_Rec_2009250,Human_Splice_Rec_2009251,Human_Splice_Rec_2009284,Human_Splice_Rec_2009285,Human_Splice_Rec_2009294,Human_Splice_Rec_2009296,Human_Splice_Rec_2009297,Human_Splice_Rec_2009303 RMVar_hsa_circ_364450 84470 RMVar_ID_84470 Human_SNP_ID_665852909 m1A Human chr19 + 40613802 40613802 40613802 CGGTGTTTGCAGGGAGGGAAGTAGCGTGAGGCAGGTTGGGGAAGGCGTGAGAGGCCTAGGAGAGC CGGTGTTTGCAGGGAGGGAAGTAGCGTGAGGCCGGTTGGGGAAGGCGTGAGAGGCCTAGGAGAGC A C LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:40613696..40613893 26863196 MeRIP-seq:(Medium) rs1042376545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8390,Human_RBP_ID_263270,Human_RBP_ID_907789,Human_RBP_ID_3588264,Human_RBP_ID_3955086,Human_RBP_ID_8233155,Human_RBP_ID_9426176,Human_RBP_ID_21979919,Human_RBP_ID_22426374,Human_RBP_ID_26336317,Human_RBP_ID_26783777,Human_RBP_ID_27815454,Human_RBP_ID_27839554 RMVar_hsa_circ_4906 84471 RMVar_ID_84471 Human_SNP_ID_665852962 m1A Human chr19 - 40613927 40613927 40613927 GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCACTCGTCAACGTCTGCGGGACAGGGCGTCCGAA GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCTCTCGTCAACGTCTGCGGGACAGGGCGTCCGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40613377..40613955 26863196 MeRIP-seq:(Medium) rs781603521 Functional Loss SNV dbSNP153 33..33 33 - - - 84472 RMVar_ID_84472 Human_SNP_ID_665852963 m1A Human chr19 - 40613927 40613927 40613927 GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCACTCGTCAACGTCTGCGGGACAGGGCGTCCGAA GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCCCTCGTCAACGTCTGCGGGACAGGGCGTCCGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40613377..40613955 26863196 MeRIP-seq:(Medium) rs781603521 Functional Loss SNV dbSNP153 33..33 33 - - - 84473 RMVar_ID_84473 Human_SNP_ID_665854666 m1A Human chr19 - 40619448 40619448 40619448 TGGGGGAACACAGCGTCCAGTCATGGGGTCAAACTCTTCCGGGCTGTTGGGGCAGACACAGAGGA TGGGGGAACACAGCGTCCAGTCATGGGGTCAAGCTCTTCCGGGCTGTTGGGGCAGACACAGAGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40619313..40619528 26863196 MeRIP-seq:(Medium) rs773660352 Functional Loss SNV dbSNP153 33..33 33 - - - 84474 RMVar_ID_84474 Human_SNP_ID_665854667 m1A Human chr19 - 40619448 40619448 40619448 TGGGGGAACACAGCGTCCAGTCATGGGGTCAAACTCTTCCGGGCTGTTGGGGCAGACACAGAGGA TGGGGGAACACAGCGTCCAGTCATGGGGTCAACCTCTTCCGGGCTGTTGGGGCAGACACAGAGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40619313..40619528 26863196 MeRIP-seq:(Medium) rs773660352 Functional Loss SNV dbSNP153 33..33 33 - - - 84475 RMVar_ID_84475 Human_SNP_ID_665855563 m1A Human chr19 + 40622690 40622690 40622690 ACCGAGACAGGTGGGCATGGGCTGATGGGGACACAGGGCTGAGGGCTTGGGTGGAAATACTGGGT ACCGAGACAGGTGGGCATGGGCTGATGGGGACCCAGGGCTGAGGGCTTGGGTGGAAATACTGGGT A C LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:40622641..40622770 26863196 MeRIP-seq:(Medium) rs762041595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31515,RMVar_hsa_circ_194897,RMVar_hsa_circ_67123,RMVar_hsa_circ_194898 84476 RMVar_ID_84476 Human_SNP_ID_665856990 m1A Human chr19 + 40627019 40627004 40627019 CCCTGTGCAATGTGCTACGCCCCCCCGCATATAGCCCCCCGCGACCAGGTGGCTTTGGACTCCCC CCCTGTGCAATGTGCTAC_______________GCCCCCCGCGACCAGGTGGCTTTGGACTCCCC CGCCCCCCCGCATATA C LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40626940..40627209 26863196 MeRIP-seq:(Medium) rs1568415393 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_522255,Human_RBP_ID_8840074,Human_RBP_ID_9293734 Human_Splice_Rec_2009088,Human_Splice_Rec_2009162,Human_Splice_Rec_2009236,Human_Splice_Rec_2009278,Human_Splice_Rec_2009326,Human_Splice_Rec_2009406,Human_Splice_Rec_2009444 RMVar_hsa_circ_31515 84477 RMVar_ID_84477 Human_SNP_ID_665857056 m1A Human chr19 + 40627113 40627113 40627113 TTACCAGGGCCTCCCATATGGGCCTGAGTTGTACCCACCACCTGCGCTACCCTACGACCCCTACC TTACCAGGGCCTCCCATATGGGCCTGAGTTGTGCCCACCACCTGCGCTACCCTACGACCCCTACC A G LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:40627076..40627150 26863196 MeRIP-seq:(Medium) rs773452069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522257,Human_RBP_ID_22973177 RMVar_hsa_circ_31515 84478 RMVar_ID_84478 Human_SNP_ID_665857288 m1A Human chr19 - 40627707 40627707 40627707 CGCCTCCAGCTCCTCGTAGGGCTCAGCCAGGGAACCTGTGGGAAATGCGGGGACCCTATGACTTG CGCCTCCAGCTCCTCGTAGGGCTCAGCCAGGGGACCTGTGGGAAATGCGGGGACCCTATGACTTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:40627701..40627852 26863196 MeRIP-seq:(Medium) rs1183941540 Functional Loss SNV dbSNP153 33..33 33 - - - 84479 RMVar_ID_84479 Human_SNP_ID_665857790 m1A Human chr19 - 40629441 40629441 40629441 AGGAGCCATCCGTGTTGAGGCAACGCGCGTTGACGCACAGCGGGGAGGCAGCCTCGGCCTCATCA AGGAGCCATCCGTGTTGAGGCAACGCGCGTTGGCGCACAGCGGGGAGGCAGCCTCGGCCTCATCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40627167..40629768 32194978 MeRIP-seq:(Medium) rs112507489 Functional Loss SNV dbSNP153 33..33 33 - - - 84480 RMVar_ID_84480 Human_SNP_ID_665857834 m1A Human chr19 + 40629513 40629513 40629513 CATCTGCCGCCCGGGATTCGCACCCACGCACCAGCCGCACCACTGTGCGCCCGCACGGCCCCGGG CATCTGCCGCCCGGGATTCGCACCCACGCACCGGCCGCACCACTGTGCGCCCGCACGGCCCCGGG A G LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40629464..40629708 26863196 MeRIP-seq:(Medium) rs958238783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522267,Human_RBP_ID_5116897 Human_miRNA_ID_272567 84481 RMVar_ID_84481 Human_SNP_ID_665867855 m1A Human chr19 - 40666854 40666854 40666854 GGGCCCAGGAGGCGGGGAGGGAGGAGGAGGAGAAGATGCGCAGTTACCTCATGTCGGTGCCCGCT GGGCCCAGGAGGCGGGGAGGGAGGAGGAGGAGGAGATGCGCAGTTACCTCATGTCGGTGCCCGCT T C NUMBL Ensembl:ENSG00000105245 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40666804..40666875 26863196 MeRIP-seq:(Medium) rs1280884782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22502967 84482 RMVar_ID_84482 Human_SNP_ID_665867951 m1A Human chr19 - 40667249 40667240 40667249 AATTCAGGGACGGACCCAGCCTGGCTAAGGGAACCATTTCACTGCCGGACTTAGGCTGGCAATGC AATTCAGGGACGGACCCAGCCTGGCTAAGGGA_________CTGCCGGACTTAGGCTGGCAATGC GTGAAATGGT G NUMBL Ensembl:ENSG00000105245 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40667198..40667298 32194978 MeRIP-seq:(Medium) rs1568425281 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_5468806,Human_RBP_ID_17384340,Human_RBP_ID_17500339,Human_RBP_ID_17925570,Human_RBP_ID_27274630,Human_RBP_ID_27468360 Human_miRNA_ID_1658228 84483 RMVar_ID_84483 Human_SNP_ID_665871986 m1A Human chr19 - 40682928 40682928 40682928 TCACGTGGAGGTAGAGGAGTCCCGGGGAATGCACGTGTGTGAAGATGCGGTGAAGAAGCTGAAGG TCACGTGGAGGTAGAGGAGTCCCGGGGAATGCTCGTGTGTGAAGATGCGGTGAAGAAGCTGAAGG T A NUMBL Ensembl:ENSG00000105245 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40682791..40683012 26863196 MeRIP-seq:(Medium) rs199917873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957004,Human_RBP_ID_6765190,Human_RBP_ID_26336319 Human_Splice_Rec_2009510,Human_Splice_Rec_2009511,Human_Splice_Rec_2009526,Human_Splice_Rec_2009527,Human_Splice_Rec_2009542,Human_Splice_Rec_2009543,Human_Splice_Rec_2009555,Human_Splice_Rec_2009574,Human_Splice_Rec_2009575,Human_Splice_Rec_2009586,Human_Splice_Rec_2009587,Human_Splice_Rec_2009592,Human_Splice_Rec_2009593,Human_Splice_Rec_2009602,Human_Splice_Rec_2009603 RMVar_hsa_circ_24238,RMVar_hsa_circ_57324 84484 RMVar_ID_84484 Human_SNP_ID_665874006 m1A Human chr19 - 40690170 40690170 40690170 ACAGGGGTACAGAGATTCTAGGTACAACTCCTAGAACTAGATGGGGATGGAGATGGGGTCGGGGA ACAGGGGTACAGAGATTCTAGGTACAACTCCTTGAACTAGATGGGGATGGAGATGGGGTCGGGGA T A NUMBL Ensembl:ENSG00000105245 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40690119..40690228 32194978 MeRIP-seq:(Medium) rs1418902370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8100651 84485 RMVar_ID_84485 Human_SNP_ID_665874062 m1A Human chr19 - 40690392 40690392 40690392 GCGGCGCCGCTGCTGATGTGGCGGAGGGTGGGAGGCGGCCGCGGCGCCCGGATGGAGAGAGGGTG GCGGCGCCGCTGCTGATGTGGCGGAGGGTGGGGGGCGGCCGCGGCGCCCGGATGGAGAGAGGGTG T C NUMBL Ensembl:ENSG00000105245 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:40690379..40690511 26863196 MeRIP-seq:(Medium) rs968875848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_263932,Human_RBP_ID_3581243,Human_RBP_ID_5239373,Human_RBP_ID_5650192,Human_RBP_ID_8100652,Human_RBP_ID_8196499,Human_RBP_ID_9330063,Human_RBP_ID_9426184,Human_RBP_ID_18461290,Human_RBP_ID_24419939,Human_RBP_ID_26784068 84486 RMVar_ID_84486 Human_SNP_ID_665877019 m1A Human chr19 + 40700167 40700167 40700167 ACAGCTCCCGCAGACACAGCGTCAGGAGCTGGAAGCAAATCTGGGGTGGGGAGAATTAACAGGCA ACAGCTCCCGCAGACACAGCGTCAGGAGCTGGTAGCAAATCTGGGGTGGGGAGAATTAACAGGCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40700116..40700401 32194978 MeRIP-seq:(Medium) rs375860406 Functional Loss SNV dbSNP153 33..33 33 - - - 84487 RMVar_ID_84487 Human_SNP_ID_665877812 m1A Human chr19 - 40703096 40703093 40703096 GATGCAGTGAGCAACGTGAGAGTCAGTATGAAAAGGAGACAGAATAGAGGCAGGCGTGACTCTGA GATGCAGTGAGCAACGTGAGAGTCAGTATGAA___GAGACAGAATAGAGGCAGGCGTGACTCTGA CCTT C COQ8B Ensembl:ENSG00000123815 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40703093..40703269 26863196 MeRIP-seq:(Medium) rs1463727805 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_194908,RMVar_hsa_circ_84628 84488 RMVar_ID_84488 Human_SNP_ID_665877884 m1A Human chr19 + 40703351 40703351 40703351 GCTCCCGTCTCTCTAAGGCTCTGTTAAAATCCATAAGGCTTTTCCCACACCTGCTCATGCTCCCT GCTCCCGTCTCTCTAAGGCTCTGTTAAAATCCGTAAGGCTTTTCCCACACCTGCTCATGCTCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40703349..40703446 26863196 MeRIP-seq:(Medium) rs116796128 Functional Loss SNV dbSNP153 33..33 33 - - - 84489 RMVar_ID_84489 Human_SNP_ID_665878369 m1A Human chr19 - 40705130 40705130 40705130 TCAGCTGCAGCACATCTTTGAGCGGGTCCGCCAGAGCGCCGACTTCATGCCCCGCTGGCAGATGC TCAGCTGCAGCACATCTTTGAGCGGGTCCGCCGGAGCGCCGACTTCATGCCCCGCTGGCAGATGC T C COQ8B Ensembl:ENSG00000123815 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40705112..40705213 32194978 MeRIP-seq:(Medium) rs1453601297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18994989,Human_RBP_ID_19090188 Human_Splice_Rec_2009630,Human_Splice_Rec_2009631,Human_Splice_Rec_2009658,Human_Splice_Rec_2009659,Human_Splice_Rec_2009684,Human_Splice_Rec_2009685,Human_Splice_Rec_2009701,Human_Splice_Rec_2009714,Human_Splice_Rec_2009715,Human_Splice_Rec_2009728,Human_Splice_Rec_2009729,Human_Splice_Rec_2009742,Human_Splice_Rec_2009743,Human_Splice_Rec_2009764 RMVar_hsa_circ_194908,RMVar_hsa_circ_84628,RMVar_hsa_circ_194909,RMVar_hsa_circ_284656,RMVar_hsa_circ_330581 84490 RMVar_ID_84490 Human_SNP_ID_665880839 m1A Human chr19 + 40714606 40714606 40714606 ACAGTCTGGCCCAGCTGTCCACCGGTCCCCCGAAGTAGGCCCCCCACCTTCAGCCACATTGCCTG ACAGTCTGGCCCAGCTGTCCACCGGTCCCCCGCAGTAGGCCCCCCACCTTCAGCCACATTGCCTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40714513..40714671 26863196 MeRIP-seq:(Medium) rs923684465 Functional Loss SNV dbSNP153 33..33 33 - - - 84491 RMVar_ID_84491 Human_SNP_ID_665881074 m1A Human chr19 + 40715376 40715375 40715377 GACAGACCCTTCTGTTCCCTACACTTTCTTGCAAAGTCTCCCTTACAAACCTGACGCCTCTCTTC GACAGACCCTTCTGTTCCCTACACTTTCTTGC__AGTCTCCCTTACAAACCTGACGCCTCTCTTC CAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40715358..40715693 26863196 MeRIP-seq:(Medium) rs1321349980 Functional Loss DEL dbSNP153 33..34 33 - - - 84492 RMVar_ID_84492 Human_SNP_ID_665881075 m1A Human chr19 + 40715376 40715376 40715376 GACAGACCCTTCTGTTCCCTACACTTTCTTGCAAAGTCTCCCTTACAAACCTGACGCCTCTCTTC GACAGACCCTTCTGTTCCCTACACTTTCTTGCGAAGTCTCCCTTACAAACCTGACGCCTCTCTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40715358..40715693 26863196 MeRIP-seq:(Medium) rs1205354315 Functional Loss SNV dbSNP153 33..33 33 - - - 84493 RMVar_ID_84493 Human_SNP_ID_665881105 m1A Human chr19 - 40715544 40715544 40715544 TATATGCACAAGGAAGGAGGTTGGGTGCCAGAATGTGGGTGTTTGTGCAAAGTGGAGGGGCTCCA TATATGCACAAGGAAGGAGGTTGGGTGCCAGAGTGTGGGTGTTTGTGCAAAGTGGAGGGGCTCCA T C COQ8B Ensembl:ENSG00000123815 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40715542..40715631 26863196 MeRIP-seq:(Medium) rs1217874267 Functional Loss SNV dbSNP153 33..33 33 - - - 84494 RMVar_ID_84494 Human_SNP_ID_665881606 m1A Human chr19 - 40717188 40717188 40717188 GCGCCTCCAGTCCCATGCGGGCCGCCGCGGGCAGCGCCCCGGCCTCCGCCTCGTTCAGGCTCCCA GCGCCTCCAGTCCCATGCGGGCCGCCGCGGGCGGCGCCCCGGCCTCCGCCTCGTTCAGGCTCCCA T C COQ8B Ensembl:ENSG00000123815 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:40717151..40717288 26863196 MeRIP-seq:(Medium) rs1377501076 Functional Loss SNV dbSNP153 33..33 33 - - - 84495 RMVar_ID_84495 Human_SNP_ID_665891003 m1A Human chr19 - 40750939 40750939 40750939 CCTGCCGCCGATGGTCGTTTGCACCGGAGGTTACCTTCCGACAGGGCCGTAGTTCTCTCAACCGG CCTGCCGCCGATGGTCGTTTGCACCGGAGGTTTCCTTCCGACAGGGCCGTAGTTCTCTCAACCGG T A C19orf54 Ensembl:ENSG00000188493 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:40750894..40751015;chr19:40750897..40751012 26863196 MeRIP-seq:(Medium) rs111978082 Functional Loss SNV dbSNP153 33..33 33 - - - 84496 RMVar_ID_84496 Human_SNP_ID_665891041 m1A Human chr19 - 40751051 40751051 40751051 CGGATGTGGGAGCCAGTATAGAAAAAAGGGACAGGTCCTAGGCAGCCTGGCCTCGAGCAGCAAGT CGGATGTGGGAGCCAGTATAGAAAAAAGGGACGGGTCCTAGGCAGCCTGGCCTCGAGCAGCAAGT T C C19orf54 Ensembl:ENSG00000188493 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:40751026..40751050 32194978 MeRIP-seq:(Medium) rs952425069 Functional Loss SNV dbSNP153 33..33 33 - - - 84497 RMVar_ID_84497 Human_SNP_ID_665891085 m1A Human chr19 - 40751174 40751174 40751174 AGAGAACTCTCGAGAGATTTACTACGACTTCCAGGATGCTCTACGCGACCCGGTGGGCGGAGCAC AGAGAACTCTCGAGAGATTTACTACGACTTCCGGGATGCTCTACGCGACCCGGTGGGCGGAGCAC T C C19orf54 Ensembl:ENSG00000188493 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:40751151..40751175 32194978 MeRIP-seq:(Medium) rs796553797 Functional Loss SNV dbSNP153 33..33 33 - - - 84498 RMVar_ID_84498 Human_SNP_ID_665891105 m1A Human chr19 - 40751231 40751231 40751231 GAGGCAAAGCGCGACAACAAAGCGTGCGTAGGACCCGCTTCTCCAGCCCGCGTGCGGAGAGAACT GAGGCAAAGCGCGACAACAAAGCGTGCGTAGGCCCCGCTTCTCCAGCCCGCGTGCGGAGAGAACT T G C19orf54 Ensembl:ENSG00000188493 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:40751201..40751357 26863196 MeRIP-seq:(Medium) rs1307480687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6765289 84499 RMVar_ID_84499 Human_SNP_ID_665891190 m1A Human chr19 + 40751422 40751422 40751422 TACCTCAACACTTCACTCCATGGCAGTTCCCGAGACCCGCCCTAACCACACTATTTATATCAACA TACCTCAACACTTCACTCCATGGCAGTTCCCGGGACCCGCCCTAACCACACTATTTATATCAACA A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40751201..40751423 26863196 MeRIP-seq:(Medium) rs528661832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522361,Human_RBP_ID_914270,Human_RBP_ID_1565956,Human_RBP_ID_8256151,Human_RBP_ID_9381040,Human_RBP_ID_13459760,Human_RBP_ID_17269388,Human_RBP_ID_17384368,Human_RBP_ID_17500364,Human_RBP_ID_17925642,Human_RBP_ID_18533192,Human_RBP_ID_26990444 Human_Splice_Rec_2009938,Human_Splice_Rec_2009939,Human_Splice_Rec_2009944,Human_Splice_Rec_2009945,Human_Splice_Rec_2009952,Human_Splice_Rec_2009953,Human_Splice_Rec_2009957,Human_Splice_Rec_2009961,Human_Splice_Rec_2009971,Human_Splice_Rec_2009981,Human_Splice_Rec_2009987 RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 84500 RMVar_ID_84500 Human_SNP_ID_665893647 m1A Human chr19 + 40759531 40759531 40759531 CCGCAAGCGGGAGAAGAGGAAGCCCAAGAGCCAGGAGACCCCGGCCACCAAGAAGGCTGTGCAAG CCGCAAGCGGGAGAAGAGGAAGCCCAAGAGCCCGGAGACCCCGGCCACCAAGAAGGCTGTGCAAG A C SNRPA Ensembl:ENSG00000077312 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40759482..40759561 26863196 MeRIP-seq:(Medium) rs1387887876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823849,Human_RBP_ID_911419,Human_RBP_ID_8233652,Human_RBP_ID_9381042,Human_RBP_ID_18470729,Human_RBP_ID_18997892,Human_RBP_ID_22448748,Human_RBP_ID_26334922,Human_RBP_ID_27815456 Human_Splice_Rec_2009931,Human_Splice_Rec_2009942,Human_Splice_Rec_2009949,Human_Splice_Rec_2009965,Human_Splice_Rec_2009975,Human_Splice_Rec_2009985 Human_miRNA_ID_2084403 RMVar_hsa_circ_112871,RMVar_hsa_circ_91364,RMVar_hsa_circ_194923,RMVar_hsa_circ_272071,RMVar_hsa_circ_194924,RMVar_hsa_circ_111605,RMVar_hsa_circ_194925,RMVar_hsa_circ_120194,RMVar_hsa_circ_194926 84501 RMVar_ID_84501 Human_SNP_ID_665895209 m1A Human chr19 - 40765082 40765082 40765082 CCTGCAGGGCATCGCGAGCTGCCCCTGCCTGTACCTCATTGTCAAACTCCACGAAGGCGATGTCA CCTGCAGGGCATCGCGAGCTGCCCCTGCCTGTTCCTCATTGTCAAACTCCACGAAGGCGATGTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40764980..40765312 26863196 MeRIP-seq:(Medium) rs1418631226 Functional Loss SNV dbSNP153 33..33 33 - - - 84502 RMVar_ID_84502 Human_SNP_ID_665895242 m1A Human chr19 - 40765199 40765199 40765199 TGAGCCAAGGGGGAAAGGGGTGGCCCCAGAACAGGGGAAGGGGCAGGCATGGGGGGAAAAGGTGC TGAGCCAAGGGGGAAAGGGGTGGCCCCAGAACGGGGGAAGGGGCAGGCATGGGGGGAAAAGGTGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:40765176..40765200 26863196 MeRIP-seq:(Medium) rs13108 Functional Loss SNV dbSNP153 33..33 33 - - - 84503 RMVar_ID_84503 Human_SNP_ID_665895276 m1A Human chr19 + 40765298 40765298 40765298 CTTGGAGCCGTGTGTGAGTGAGTGGTCGCCACACAGCATTGTACCCAGAGTCTGTCCCCAGACAT CTTGGAGCCGTGTGTGAGTGAGTGGTCGCCACGCAGCATTGTACCCAGAGTCTGTCCCCAGACAT A G SNRPA Ensembl:ENSG00000077312 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40765248..40765317 26863196 MeRIP-seq:(Medium) rs527486727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522374,Human_RBP_ID_1565991,Human_RBP_ID_1888309,Human_RBP_ID_3572302,Human_RBP_ID_5116272,Human_RBP_ID_8488215,Human_RBP_ID_9088129,Human_RBP_ID_9328955,Human_RBP_ID_17081865,Human_RBP_ID_17655357,Human_RBP_ID_17925657,Human_RBP_ID_18192274,Human_RBP_ID_18441461,Human_RBP_ID_18946880,Human_RBP_ID_23798529,Human_RBP_ID_25418879 Human_miRNA_ID_322856,Human_miRNA_ID_2076642,Human_miRNA_ID_2425655,Human_miRNA_ID_2435323 RMVar_hsa_circ_80426,RMVar_hsa_circ_112871,RMVar_hsa_circ_91364,RMVar_hsa_circ_194923,RMVar_hsa_circ_194925,RMVar_hsa_circ_120194,RMVar_hsa_circ_194926,RMVar_hsa_circ_124527,RMVar_hsa_circ_122642,RMVar_hsa_circ_194927,RMVar_hsa_circ_194928,RMVar_hsa_circ_194929 84504 RMVar_ID_84504 Human_SNP_ID_665898840 m1A Human chr19 + 40778305 40778305 40778305 GTAGGAAGGAGCCGGGGCTGTAGCCGGAGTGGAGCGGCTGCCAGCCGAGGAGCAGGCGCGGCCGC GTAGGAAGGAGCCGGGGCTGTAGCCGGAGTGGCGCGGCTGCCAGCCGAGGAGCAGGCGCGGCCGC A C RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding 5'UTR,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40778258..40779111 26863196 MeRIP-seq:(Medium) rs1316684618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3586430,Human_RBP_ID_4558475 Human_Splice_Rec_2010055,Human_Splice_Rec_2010069,Human_Splice_Rec_2010083,Human_Splice_Rec_2010091,Human_Splice_Rec_2010097,Human_Splice_Rec_2010109,Human_Splice_Rec_2010135,Human_Splice_Rec_2010141 84505 RMVar_ID_84505 Human_SNP_ID_665898841 m1A Human chr19 + 40778305 40778305 40778305 GTAGGAAGGAGCCGGGGCTGTAGCCGGAGTGGAGCGGCTGCCAGCCGAGGAGCAGGCGCGGCCGC GTAGGAAGGAGCCGGGGCTGTAGCCGGAGTGGGGCGGCTGCCAGCCGAGGAGCAGGCGCGGCCGC A G RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding 5'UTR,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40778258..40779111 26863196 MeRIP-seq:(Medium) rs1316684618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3586430,Human_RBP_ID_4558475 Human_Splice_Rec_2010055,Human_Splice_Rec_2010069,Human_Splice_Rec_2010083,Human_Splice_Rec_2010091,Human_Splice_Rec_2010097,Human_Splice_Rec_2010109,Human_Splice_Rec_2010135,Human_Splice_Rec_2010141 84506 RMVar_ID_84506 Human_SNP_ID_665898847 m1A Human chr19 + 40778323 40778323 40778323 TGTAGCCGGAGTGGAGCGGCTGCCAGCCGAGGAGCAGGCGCGGCCGCGGCGCCATATTGCGGCCC TGTAGCCGGAGTGGAGCGGCTGCCAGCCGAGGGGCAGGCGCGGCCGCGGCGCCATATTGCGGCCC A G RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding 5'UTR,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40778273..40778573 26863196 MeRIP-seq:(Medium) rs867963271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3586430,Human_RBP_ID_4558475 Human_Splice_Rec_2010055,Human_Splice_Rec_2010069,Human_Splice_Rec_2010083,Human_Splice_Rec_2010091,Human_Splice_Rec_2010097,Human_Splice_Rec_2010109,Human_Splice_Rec_2010135,Human_Splice_Rec_2010141 84507 RMVar_ID_84507 Human_SNP_ID_665899472 m1A Human chr19 - 40780510 40780510 40780510 TCACTCTCTCTCCCCATCACCCTTGGGAGCCCAGCCCACCTACCGAAACCGCTCCTGGCCAGCCG TCACTCTCTCTCCCCATCACCCTTGGGAGCCCTGCCCACCTACCGAAACCGCTCCTGGCCAGCCG T A AC008537.4 Ensembl:ENSG00000282951 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40780462..40783840 26863196 MeRIP-seq:(Medium) rs1235395287 Functional Loss SNV dbSNP153 33..33 33 - - - 84508 RMVar_ID_84508 Human_SNP_ID_665901030 m1A Human chr19 + 40785849 40785849 40785849 GTGAGGGTGGAAGGACAGACCCACTTCCAGACAGTGACACCTCAGGAAGGTCAGGGCTTGATGGT GTGAGGGTGGAAGGACAGACCCACTTCCAGACGGTGACACCTCAGGAAGGTCAGGGCTTGATGGT A G RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40785843..40786011 26863196 MeRIP-seq:(Medium) rs1216797092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13460173 RMVar_hsa_circ_194931,RMVar_hsa_circ_324458,RMVar_hsa_circ_272845,RMVar_hsa_circ_194932 84509 RMVar_ID_84509 Human_SNP_ID_665901171 m1A Human chr19 + 40786337 40786337 40786337 TGGGATGGGGACCCAGGCAGAGGGTTGGGGCCAGGATGAGGAAGCACAAGCAGTGGGGTCAGGGC TGGGATGGGGACCCAGGCAGAGGGTTGGGGCCGGGATGAGGAAGCACAAGCAGTGGGGTCAGGGC A G RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40786322..40786522 26863196 MeRIP-seq:(Medium) rs1013388856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9427322 RMVar_hsa_circ_194931,RMVar_hsa_circ_324458,RMVar_hsa_circ_272845,RMVar_hsa_circ_194932 84510 RMVar_ID_84510 Human_SNP_ID_665904966 m1A Human chr19 - 40799260 40799260 40799260 CGCTCCCTTCTCGCCCCGCGACCTCCTCACCGAGCTTTTTCCTCCGGCCCCGGCGCCGCCGTTTG CGCTCCCTTCTCGCCCCGCGACCTCCTCACCGCGCTTTTTCCTCCGGCCCCGGCGCCGCCGTTTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:40799201..40799323;chr19:40799176..40799495 26863196 MeRIP-seq:(Medium) rs1275952133 Functional Loss SNV dbSNP153 33..33 33 - - - 84511 RMVar_ID_84511 Human_SNP_ID_665905484 m1A Human chr19 + 40800577 40800577 40800577 ATGCCCGGGGGATGAAGACACTGCTGCCATGGACAGCCCGTGCCAGCCGCAGCCCCTAAGTCAGG ATGCCCGGGGGATGAAGACACTGCTGCCATGGGCAGCCCGTGCCAGCCGCAGCCCCTAAGTCAGG A G EGLN2,RAB4B-EGLN2 Ensembl:ENSG00000269858,Ensembl:ENSG00000171570 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40800326..40801434 26863196 MeRIP-seq:(Medium) rs1228124095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908705,Human_RBP_ID_13460329,Human_RBP_ID_18165763,Human_RBP_ID_18733553,Human_RBP_ID_27468405 RMVar_hsa_circ_93768,RMVar_hsa_circ_194934,RMVar_hsa_circ_194935,RMVar_hsa_circ_83680 84512 RMVar_ID_84512 Human_SNP_ID_665905573 m1A Human chr19 + 40800735 40800735 40800735 TGCTCCCCTCCTACCACTGTCCAGGAGTGCCTAGTGAGGCCTCGGCAGGGAGTGGGACCCCCAGA TGCTCCCCTCCTACCACTGTCCAGGAGTGCCTGGTGAGGCCTCGGCAGGGAGTGGGACCCCCAGA A G EGLN2,RAB4B-EGLN2 Ensembl:ENSG00000269858,Ensembl:ENSG00000171570 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40786977..40892015 32194978 MeRIP-seq:(Medium) rs970787709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240618,Human_RBP_ID_522389,Human_RBP_ID_1566085,Human_RBP_ID_4530844,Human_RBP_ID_5146313,Human_RBP_ID_5321671,Human_RBP_ID_8488288,Human_RBP_ID_9330067,Human_RBP_ID_17925678,Human_RBP_ID_23798595,Human_RBP_ID_27274714 RMVar_hsa_circ_93768,RMVar_hsa_circ_194934,RMVar_hsa_circ_194935,RMVar_hsa_circ_83680 84513 RMVar_ID_84513 Human_SNP_ID_665905720 m1A Human chr19 + 40801051 40801051 40801051 CATGAGCTGCAGCTGCAGCAGTGGCAGTGGTGAGGCCAGTGCTGGGCTGATGGAGGAGGCGCTGC CATGAGCTGCAGCTGCAGCAGTGGCAGTGGTGGGGCCAGTGCTGGGCTGATGGAGGAGGCGCTGC A G EGLN2,RAB4B-EGLN2 Ensembl:ENSG00000269858,Ensembl:ENSG00000171570 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40801004..40801325 26863196 MeRIP-seq:(Medium) rs201258123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581248,Human_RBP_ID_3955100,Human_RBP_ID_5320401,Human_RBP_ID_8834401,Human_RBP_ID_27468417,Human_RBP_ID_27562521 Human_miRNA_ID_2156413,Human_miRNA_ID_2156414,Human_miRNA_ID_2159973,Human_miRNA_ID_2159974,Human_miRNA_ID_2172528,Human_miRNA_ID_2172529 Clinvar_Rec_438,Clinvar_Rec_3866 RMVar_hsa_circ_93768,RMVar_hsa_circ_194934,RMVar_hsa_circ_194935,RMVar_hsa_circ_83680 84514 RMVar_ID_84514 Human_SNP_ID_665906979 m1A Human chr19 + 40805158 40805158 40805158 TTATCTTGGGACTGTCTTGCTGGGCCGGGCCCATAGGTGTAGCTGAGCATTCGTGGGGAATGGAC TTATCTTGGGACTGTCTTGCTGGGCCGGGCCCGTAGGTGTAGCTGAGCATTCGTGGGGAATGGAC A G EGLN2,RAB4B-EGLN2,AC008537.1 Ensembl:ENSG00000269858,Ensembl:ENSG00000171570,Ensembl:ENSG00000268797 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40805152..40805217 26863196 MeRIP-seq:(Medium) rs1030195178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588288,Human_RBP_ID_6765608,Human_RBP_ID_8103026,Human_RBP_ID_13460432,Human_RBP_ID_17132584,Human_RBP_ID_27680393 RMVar_hsa_circ_93768,RMVar_hsa_circ_194934,RMVar_hsa_circ_194935,RMVar_hsa_circ_83680 84515 RMVar_ID_84515 Human_SNP_ID_665912101 m1A Human chr19 - 40823866 40823866 40823866 TGCACAAGCCAACCTTTCGCCCTCACTGACCCACTTCCTCCCAGGCCCTGGCTAACTCTTTTTTT TGCACAAGCCAACCTTTCGCCCTCACTGACCCCCTTCCTCCCAGGCCCTGGCTAACTCTTTTTTT T G CYP2F2P Ensembl:ENSG00000237118 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40823842..40824276 26863196 MeRIP-seq:(Medium) rs987001182 Functional Loss SNV dbSNP153 33..33 33 - - - 84516 RMVar_ID_84516 Human_SNP_ID_665919596 m1A Human chr19 + 40849009 40849009 40849009 AAGAGAGAGAGGAGAGAGAGAGAGAGAGAGAGAGAAGAGAGAGAGGAGAGAGAGAGAGAAGAGAG AAGAGAGAGAGGAGAGAGAGAGAGAGAGAGAGCGAAGAGAGAGAGGAGAGAGAGAGAGAAGAGAG A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40848897..40849204 26863196 MeRIP-seq:(Medium) rs989068215 Functional Loss SNV dbSNP153 33..33 33 - - - 84517 RMVar_ID_84517 Human_SNP_ID_665919597 m1A Human chr19 + 40849009 40849009 40849009 AAGAGAGAGAGGAGAGAGAGAGAGAGAGAGAGAGAAGAGAGAGAGGAGAGAGAGAGAGAAGAGAG AAGAGAGAGAGGAGAGAGAGAGAGAGAGAGAGGGAAGAGAGAGAGGAGAGAGAGAGAGAAGAGAG A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40848897..40849204 26863196 MeRIP-seq:(Medium) rs989068215 Functional Loss SNV dbSNP153 33..33 33 - - - 84518 RMVar_ID_84518 Human_SNP_ID_665919757 m1A Human chr19 + 40849128 40849124 40849128 TTAAAGAATAAGACAATCAGAAAAGAAACAGAAAGGCCAGACAGAGAGATGCACATAGAAACAGA TTAAAGAATAAGACAATCAGAAAAGAAAC____AGGCCAGACAGAGAGATGCACATAGAAACAGA CAGAA C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40848837..40849212 26863196 MeRIP-seq:(Medium) rs1011727602 Functional Loss DEL dbSNP153 30..33 33 - - - 84519 RMVar_ID_84519 Human_SNP_ID_665919807 m1A Human chr19 + 40849321 40849321 40849321 AGATTCTTAAGCTGAGCTGGAGAAGAGAGAAAAATATTGAGATAGAAACAGAGAGGGTCTGGAAG AGATTCTTAAGCTGAGCTGGAGAAGAGAGAAATATATTGAGATAGAAACAGAGAGGGTCTGGAAG A T AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40849270..40849518 26863196 MeRIP-seq:(Medium) rs1468137152 Functional Loss SNV dbSNP153 33..33 33 - - - 84520 RMVar_ID_84520 Human_SNP_ID_665919822 m1A Human chr19 + 40849374 40849374 40849374 AGGGTCTGGAAGGAAGAGAGACTGTTACCAGGAGATGGAGGCTGAAGATGTGGAAGTAGGAATAC AGGGTCTGGAAGGAAGAGAGACTGTTACCAGGTGATGGAGGCTGAAGATGTGGAAGTAGGAATAC A T AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40849324..40849563 26863196 MeRIP-seq:(Medium) rs1323211883 Functional Loss SNV dbSNP153 33..33 33 - - - 84521 RMVar_ID_84521 Human_SNP_ID_665929207 m1A Human chr19 - 40881436 40881436 40881436 ATCTCCCCATCTCCCTTCACTGTGGCCTCTCCATGTGTATCCCTCACCTGTCTCCAGCGTCCCTG ATCTCCCCATCTCCCTTCACTGTGGCCTCTCCCTGTGTATCCCTCACCTGTCTCCAGCGTCCCTG T G CYP2A7 Ensembl:ENSG00000198077 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40881404..40881469 26863196 MeRIP-seq:(Medium) rs1189304530 Functional Loss SNV dbSNP153 33..33 33 - - - 84522 RMVar_ID_84522 Human_SNP_ID_665950411 m1A Human chr19 + 40959688 40959688 40959688 CTTTCTGTCTCTCTCTCTTCTCTCTCTCTCTTAATCTGTCTCAACACCCCATGTCTCCCTGGTGC CTTTCTGTCTCTCTCTCTTCTCTCTCTCTCTTCATCTGTCTCAACACCCCATGTCTCCCTGGTGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40959538..40959949 26863196 MeRIP-seq:(Medium) rs1446283960 Functional Loss SNV dbSNP153 33..33 33 - - - 84523 RMVar_ID_84523 Human_SNP_ID_665950571 m1A Human chr19 - 40960084 40960084 40960084 AGAGAAAGACAGAGACAGAGAGGGAGAGAGAGAGAAGACAGACAGAGATGGACAGAGAGAGAAAG AGAGAAAGACAGAGACAGAGAGGGAGAGAGAGTGAAGACAGACAGAGATGGACAGAGAGAGAAAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40959682..40960441 26863196 MeRIP-seq:(Medium) rs1047313161 Functional Loss SNV dbSNP153 33..33 33 - - - 84524 RMVar_ID_84524 Human_SNP_ID_666016830 m1A Human chr19 + 41193102 41193102 41193102 CCCGACATCAGGCGGCGGCGGTGGTCCGGGAGAAACCCGGCGGCGGGGAGATAAGCCTGCCCAGG CCCGACATCAGGCGGCGGCGGTGGTCCGGGAGTAACCCGGCGGCGGGGAGATAAGCCTGCCCAGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41193065..41193207 26863196 MeRIP-seq:(Medium) rs1415515686 Functional Loss SNV dbSNP153 33..33 33 - - - 84525 RMVar_ID_84525 Human_SNP_ID_666016936 m1A Human chr19 - 41193311 41193311 41193311 TGGTCCCGGACAGCGCCAGCGTCAGCAGCAGGAGCAGCGCCAGCGCCAGCAGCAGCGCCCAGGTG TGGTCCCGGACAGCGCCAGCGTCAGCAGCAGGCGCAGCGCCAGCGCCAGCAGCAGCGCCCAGGTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41193260..41193498 26863196 MeRIP-seq:(Medium) rs889471733 Functional Loss SNV dbSNP153 33..33 33 - - - 84526 RMVar_ID_84526 Human_SNP_ID_666017352 m1A Human chr19 + 41194689 41194689 41194689 GTTCAGCGGCCGGGGAACCGTAGCGATGCTGGAAGGGACTTTTGATGGCCATGGTAAGTCAAGGG GTTCAGCGGCCGGGGAACCGTAGCGATGCTGGGAGGGACTTTTGATGGCCATGGTAAGTCAAGGG A G CYP2S1 Ensembl:ENSG00000167600 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41193225..41197921 26863196 MeRIP-seq:(Medium) rs1295892454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2010587,Human_Splice_Rec_2010603,Human_Splice_Rec_2010613,Human_Splice_Rec_2010619 RMVar_hsa_circ_113894,RMVar_hsa_circ_194939 84527 RMVar_ID_84527 Human_SNP_ID_666024324 m1A Human chr19 - 41219450 41219450 41219450 CTCACCCCTGGGGGCCATGCACGCCCAGCCGCACAGCGCCAAGCACCAGGCCAGCGGGACCCTGC CTCACCCCTGGGGGCCATGCACGCCCAGCCGCGCAGCGCCAAGCACCAGGCCAGCGGGACCCTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41219401..41219500 32194978 MeRIP-seq:(Medium) rs753148751 Functional Loss SNV dbSNP153 33..33 33 - - - 84528 RMVar_ID_84528 Human_SNP_ID_666030102 m1A Human chr19 - 41240049 41240049 41240049 CATCCATCTACCCATCCATTTATCCACTCGACATCCAGTCATTTATCTGTTCACCCGCCTATCCA CATCCATCTACCCATCCATTTATCCACTCGACTTCCAGTCATTTATCTGTTCACCCGCCTATCCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41240045..41240188 26863196 MeRIP-seq:(Medium) rs1295084930 Functional Loss SNV dbSNP153 33..33 33 - - - 84529 RMVar_ID_84529 Human_SNP_ID_666036419 m1A Human chr19 + 41264504 41264504 41264504 CGGGCTCGGGGGCCACCCCGGGGGCCCGGGCCATGGATGTGCGCCGTCTGAAGGTGAACGAACTT CGGGCTCGGGGGCCACCCCGGGGGCCCGGGCCGTGGATGTGCGCCGTCTGAAGGTGAACGAACTT A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:41264401..41264575 26863410 MeRIP-seq:(Medium) rs771866921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1566119,Human_RBP_ID_1888372,Human_RBP_ID_4530986,Human_RBP_ID_5469605,Human_RBP_ID_8834414,Human_RBP_ID_9294431,Human_RBP_ID_9328960,Human_RBP_ID_9381046,Human_RBP_ID_22811000,Human_RBP_ID_23798732 84530 RMVar_ID_84530 Human_SNP_ID_666036511 m1A Human chr19 + 41264691 41264691 41264691 CGAACCGGGGCGACCCGGGCACATCAACGAGGAGGTCGAGACCGAGGGGGGCTCCGAGCTGGAGG CGAACCGGGGCGACCCGGGCACATCAACGAGGTGGTCGAGACCGAGGGGGGCTCCGAGCTGGAGG A T HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41264351..41265335 26863196 MeRIP-seq:(Medium) rs748306861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241356,Human_RBP_ID_4560224,Human_RBP_ID_6765725,Human_RBP_ID_8834419,Human_RBP_ID_9381048,Human_RBP_ID_18441472,Human_RBP_ID_18733611,Human_RBP_ID_22502996,Human_RBP_ID_26334925,Human_RBP_ID_27468459,Human_RBP_ID_27562537 Human_Splice_Rec_2010911,Human_Splice_Rec_2010939 84531 RMVar_ID_84531 Human_SNP_ID_666036670 m1A Human chr19 + 41265151 41265151 41265151 GAGGTTTTCCGTTTGGGTTGGGGAGGGTCTCGAAAATGGGGATCCTAGGGTACGGAGCTCCGTGG GAGGTTTTCCGTTTGGGTTGGGGAGGGTCTCGGAAATGGGGATCCTAGGGTACGGAGCTCCGTGG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:41265105..41265350 26863196 MeRIP-seq:(Medium) rs117710350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3581265,Human_RBP_ID_5320406,Human_RBP_ID_6765730,Human_RBP_ID_8100664,Human_RBP_ID_8196508,Human_RBP_ID_9425339,Human_RBP_ID_17190832,Human_RBP_ID_18490715,Human_RBP_ID_18945484,Human_RBP_ID_21977982 Human_Splice_Rec_2010981 84532 RMVar_ID_84532 Human_SNP_ID_666036783 m1A Human chr19 - 41265528 41265528 41265528 CAACCAGAAAGTCCCCAGATCTCCCAGCACCTAATGTCCAGGCTGTGCCTGCTTCAAGGGTGGCC CAACCAGAAAGTCCCCAGATCTCCCAGCACCTGATGTCCAGGCTGTGCCTGCTTCAAGGGTGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41265525..41266008 26863196 MeRIP-seq:(Medium) rs1010242714 Functional Loss SNV dbSNP153 33..33 33 - - - 84533 RMVar_ID_84533 Human_SNP_ID_666036784 m1A Human chr19 - 41265528 41265528 41265528 CAACCAGAAAGTCCCCAGATCTCCCAGCACCTAATGTCCAGGCTGTGCCTGCTTCAAGGGTGGCC CAACCAGAAAGTCCCCAGATCTCCCAGCACCTCATGTCCAGGCTGTGCCTGCTTCAAGGGTGGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41265525..41266008 26863196 MeRIP-seq:(Medium) rs1010242714 Functional Loss SNV dbSNP153 33..33 33 - - - 84534 RMVar_ID_84534 Human_SNP_ID_666037420 m1A Human chr19 + 41268280 41268280 41268280 GAACCAATTCTACGATACCCAAGTCATCAAACAAGAAAACGAGTCAGGCTACGAGAGGAGACCAC GAACCAATTCTACGATACCCAAGTCATCAAACGAGAAAACGAGTCAGGCTACGAGAGGAGACCAC A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:41268201..41268300 26863196 MeRIP-seq:(Medium) rs1377934972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914778,Human_RBP_ID_1016318,Human_RBP_ID_1566149,Human_RBP_ID_1888385,Human_RBP_ID_4531022,Human_RBP_ID_6765797,Human_RBP_ID_8834425,Human_RBP_ID_9381049,Human_RBP_ID_13460764,Human_RBP_ID_17269398,Human_RBP_ID_17925737,Human_RBP_ID_18305474,Human_RBP_ID_18532511,Human_RBP_ID_24545594,Human_RBP_ID_26336325,Human_RBP_ID_26990508 Human_Splice_Rec_2010768,Human_Splice_Rec_2010769,Human_Splice_Rec_2010796,Human_Splice_Rec_2010797,Human_Splice_Rec_2010834,Human_Splice_Rec_2010835,Human_Splice_Rec_2010852,Human_Splice_Rec_2010853,Human_Splice_Rec_2010860,Human_Splice_Rec_2010861,Human_Splice_Rec_2010884,Human_Splice_Rec_2010885,Human_Splice_Rec_2010912,Human_Splice_Rec_2010913,Human_Splice_Rec_2010944,Human_Splice_Rec_2010945,Human_Splice_Rec_2010974,Human_Splice_Rec_2010975,Human_Splice_Rec_2010982,Human_Splice_Rec_2010983,Human_Splice_Rec_2011010,Human_Splice_Rec_2011011,Human_Splice_Rec_2011022,Human_Splice_Rec_2011023,Human_Splice_Rec_2011049,Human_Splice_Rec_2011051 Human_miRNA_ID_2454613 RMVar_hsa_circ_194998,RMVar_hsa_circ_327105,RMVar_hsa_circ_340117,RMVar_hsa_circ_348795,RMVar_hsa_circ_351270,RMVar_hsa_circ_347393,RMVar_hsa_circ_331084,RMVar_hsa_circ_276078,RMVar_hsa_circ_308631,RMVar_hsa_circ_311027,RMVar_hsa_circ_306334,RMVar_hsa_circ_195000,RMVar_hsa_circ_195001,RMVar_hsa_circ_194999 84535 RMVar_ID_84535 Human_SNP_ID_666038523 m1A Human chr19 + 41272195 41272195 41272195 AATTCCAGAGTCGAAAGAGGCCTTATGAAGAAAACCGGGGACGGGGGTACTTTGAGCACCGAGAG AATTCCAGAGTCGAAAGAGGCCTTATGAAGAAGACCGGGGACGGGGGTACTTTGAGCACCGAGAG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41272176..41272200 26863196 MeRIP-seq:(Medium) rs1209277520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279681,Human_RBP_ID_1016320,Human_RBP_ID_1566158,Human_RBP_ID_1888387,Human_RBP_ID_3957010,Human_RBP_ID_4531031,Human_RBP_ID_6765813,Human_RBP_ID_8840610,Human_RBP_ID_9292308,Human_RBP_ID_9381054,Human_RBP_ID_13460843,Human_RBP_ID_17269401,Human_RBP_ID_17925740,Human_RBP_ID_18441474,Human_RBP_ID_23131370,Human_RBP_ID_26336327,Human_RBP_ID_27815461 Human_Splice_Rec_2010771,Human_Splice_Rec_2010799,Human_Splice_Rec_2010825,Human_Splice_Rec_2010837,Human_Splice_Rec_2010855,Human_Splice_Rec_2010863,Human_Splice_Rec_2010887,Human_Splice_Rec_2010915,Human_Splice_Rec_2010947,Human_Splice_Rec_2010977,Human_Splice_Rec_2010985,Human_Splice_Rec_2011013,Human_Splice_Rec_2011025,Human_Splice_Rec_2011053 Human_miRNA_ID_1967501 RMVar_hsa_circ_194998,RMVar_hsa_circ_340117,RMVar_hsa_circ_348795,RMVar_hsa_circ_351270,RMVar_hsa_circ_347393,RMVar_hsa_circ_331084,RMVar_hsa_circ_276078,RMVar_hsa_circ_308631,RMVar_hsa_circ_311027,RMVar_hsa_circ_306334,RMVar_hsa_circ_195000,RMVar_hsa_circ_194999,RMVar_hsa_circ_279473,RMVar_hsa_circ_354097,RMVar_hsa_circ_375137,RMVar_hsa_circ_195002 84536 RMVar_ID_84536 Human_SNP_ID_666038990 m1A Human chr19 - 41274021 41274021 41274021 GTGTCAATAGCAACAAGGGTATCATCAAAGTCATCTTCATCCTCTTCAGCAGGAGGCTGAGGAGA GTGTCAATAGCAACAAGGGTATCATCAAAGTCGTCTTCATCCTCTTCAGCAGGAGGCTGAGGAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41273976..41274025 26863196 MeRIP-seq:(Medium) rs750031273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195003 84537 RMVar_ID_84537 Human_SNP_ID_666044277 m1A Human chr19 + 41294311 41294299 41294312 CCGAGCCAAGTGGTGCCATACCACCATGCCGCAACACCTTCCCTGTCTTGTTCTTGTAGATTCTG CCGAGCCAAGTGGTGCCATAC_____________CACCTTCCCTGTCTTGTTCTTGTAGATTCTG CCACCATGCCGCAA C HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41294306..41294405 26863196 MeRIP-seq:(Medium) rs780818495 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_194998,RMVar_hsa_circ_348795,RMVar_hsa_circ_331084,RMVar_hsa_circ_306334,RMVar_hsa_circ_24100,RMVar_hsa_circ_364694 84538 RMVar_ID_84538 Human_SNP_ID_666044309 m1A Human chr19 + 41294473 41294473 41294473 CCATCATGGATAAGATGCGGGTAAGGCCAGCCACTGGACTCTCCTTACTCACCTCCAACCTACTG CCATCATGGATAAGATGCGGGTAAGGCCAGCCGCTGGACTCTCCTTACTCACCTCCAACCTACTG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41294469..41294536 26863196 MeRIP-seq:(Medium) rs771359373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090208 RMVar_hsa_circ_194998,RMVar_hsa_circ_348795,RMVar_hsa_circ_331084,RMVar_hsa_circ_306334,RMVar_hsa_circ_24100,RMVar_hsa_circ_364694 84539 RMVar_ID_84539 Human_SNP_ID_666046235 m1A Human chr19 + 41302751 41302751 41302751 AGCTGCAGCGGGAGGAAGCGGACAAGCTAGTGAGGCAGTACAACGAGGAAGGCCGCAAGGCTGGG AGCTGCAGCGGGAGGAAGCGGACAAGCTAGTGGGGCAGTACAACGAGGAAGGCCGCAAGGCTGGG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:41302701..41302991;chr19:41302701..41302899 26863196 MeRIP-seq:(Medium) rs948549590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53240,Human_RBP_ID_1016345,Human_RBP_ID_1888434,Human_RBP_ID_5373935,Human_RBP_ID_6766000,Human_RBP_ID_8488427,Human_RBP_ID_8839370,Human_RBP_ID_9293751,Human_RBP_ID_13461572,Human_RBP_ID_18441485,Human_RBP_ID_26336337 Human_Splice_Rec_2010788,Human_Splice_Rec_2010816,Human_Splice_Rec_2010876,Human_Splice_Rec_2010904,Human_Splice_Rec_2010932,Human_Splice_Rec_2010964,Human_Splice_Rec_2011002,Human_Splice_Rec_2011042,Human_Splice_Rec_2011070 Human_miRNA_ID_2477901 RMVar_hsa_circ_331084,RMVar_hsa_circ_115787,RMVar_hsa_circ_33023,RMVar_hsa_circ_195007 84540 RMVar_ID_84540 Human_SNP_ID_666046247 m1A Human chr19 + 41302786 41302786 41302786 CAGTACAACGAGGAAGGCCGCAAGGCTGGGCCACCCCCTGAAAAGCGCTTTGACAACCGAGGTGG CAGTACAACGAGGAAGGCCGCAAGGCTGGGCCGCCCCCTGAAAAGCGCTTTGACAACCGAGGTGG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:41302736..41302850 26863196 MeRIP-seq:(Medium) rs1277561188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239683,Human_RBP_ID_1190129,Human_RBP_ID_6766003,Human_RBP_ID_8839370,Human_RBP_ID_9293751,Human_RBP_ID_18733699,Human_RBP_ID_26336337 Human_miRNA_ID_1551317,Human_miRNA_ID_2795881,Human_miRNA_ID_2796711,Human_miRNA_ID_2797128,Human_miRNA_ID_2799475 RMVar_hsa_circ_331084,RMVar_hsa_circ_115787,RMVar_hsa_circ_33023,RMVar_hsa_circ_195007 84541 RMVar_ID_84541 Human_SNP_ID_666046654 m1A Human chr19 + 41304128 41304128 41304128 GCAGCCTCCGCCACCACAGCCACCACCCCAGCAGCCACCGCCACCACCCAGCTACAGCCCTGCTC GCAGCCTCCGCCACCACAGCCACCACCCCAGCGGCCACCGCCACCACCCAGCTACAGCCCTGCTC A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr19:41304077..41306450;chr19:41304026..41304312 26863196,26863410 MeRIP-seq:(Medium) rs756376502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8256167,Human_RBP_ID_17386852,Human_RBP_ID_20349440 Human_miRNA_ID_2686262 RMVar_hsa_circ_15032,RMVar_hsa_circ_331084,RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 84542 RMVar_ID_84542 Human_SNP_ID_666047050 m1A Human chr19 + 41305735 41305735 41305735 CAGGGAGGTTACAGCCAGGGCTACACAGCCCCACCGCCTCCACCTCCACCACCACCTGCCTACAA CAGGGAGGTTACAGCCAGGGCTACACAGCCCCCCCGCCTCCACCTCCACCACCACCTGCCTACAA A C HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:41305650..41305839 26863196 MeRIP-seq:(Medium) rs1204030073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4531140,Human_RBP_ID_6766023,Human_RBP_ID_8488436,Human_RBP_ID_17269419,Human_RBP_ID_17384386,Human_RBP_ID_22973410,Human_RBP_ID_26468449,Human_RBP_ID_27815463 Human_Splice_Rec_2010792,Human_Splice_Rec_2010820,Human_Splice_Rec_2010880,Human_Splice_Rec_2010908,Human_Splice_Rec_2010936,Human_Splice_Rec_2010942,Human_Splice_Rec_2011006,Human_Splice_Rec_2011046,Human_Splice_Rec_2011090 RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 84543 RMVar_ID_84543 Human_SNP_ID_666047110 m1A Human chr19 + 41305851 41305851 41305851 CCCCACTGCACAGACCTACCCTCAGCCCAGCTATAACCAGTATCAGCAGGTAGGTGCCAGACTGG CCCCACTGCACAGACCTACCCTCAGCCCAGCTTTAACCAGTATCAGCAGGTAGGTGCCAGACTGG A T HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:41305801..41305875 26863196 MeRIP-seq:(Medium) rs746897314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522441,Human_RBP_ID_6766026,Human_RBP_ID_17269422,Human_RBP_ID_17386855,Human_RBP_ID_17500393,Human_RBP_ID_18946890,Human_RBP_ID_27468466 Human_Splice_Rec_2010793,Human_Splice_Rec_2010821,Human_Splice_Rec_2010881,Human_Splice_Rec_2010909,Human_Splice_Rec_2010937,Human_Splice_Rec_2010968,Human_Splice_Rec_2010969,Human_Splice_Rec_2010971,Human_Splice_Rec_2011007,Human_Splice_Rec_2011047,Human_Splice_Rec_2011091 RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 84544 RMVar_ID_84544 Human_SNP_ID_666047296 m1A Human chr19 - 41306597 41306597 41306597 GGCCGAGGCAGGCGCTGGTGGAGGAAGCCGGCAGGGGCCTCCGGGAGCCTCTGGGTCACACTGGC GGCCGAGGCAGGCGCTGGTGGAGGAAGCCGGCCGGGGCCTCCGGGAGCCTCTGGGTCACACTGGC T G TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41306459..41306939 26863196 MeRIP-seq:(Medium) rs746159786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195008 84545 RMVar_ID_84545 Human_SNP_ID_666047301 m1A Human chr19 + 41306611 41306611 41306611 GAGGCTCCCGGAGGCCCCTGCCGGCTTCCTCCACCAGCGCCTGCCTCGGCCCCTCCTCTGCCCCC GAGGCTCCCGGAGGCCCCTGCCGGCTTCCTCCCCCAGCGCCTGCCTCGGCCCCTCCTCTGCCCCC A C HNRNPUL1 Ensembl:ENSG00000105323 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:41306526..41306744 26863196 MeRIP-seq:(Medium) rs753129898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522447,Human_RBP_ID_4531148,Human_RBP_ID_6766033,Human_RBP_ID_8488441,Human_RBP_ID_13461658,Human_RBP_ID_17657086,Human_RBP_ID_17935403,Human_RBP_ID_18733720,Human_RBP_ID_27274794 Human_miRNA_ID_272570 84546 RMVar_ID_84546 Human_SNP_ID_666048236 m1A Human chr19 - 41310269 41310269 41310269 CTCGGACTTTTCAACCGCCCGGCGGGCCCCGCACACTAACCTCCGGCCCACGCACGCAAGAGACA CTCGGACTTTTCAACCGCCCGGCGGGCCCCGCGCACTAACCTCCGGCCCACGCACGCAAGAGACA T C AC011462.5,TGFB1 Ensembl:ENSG00000286177,Ensembl:ENSG00000105329 lincRNA,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:41310218..41310381;chr19:41310225..41310388 26863196 MeRIP-seq:(Medium) rs1346302816 Functional Loss SNV dbSNP153 33..33 33 - - - 84547 RMVar_ID_84547 Human_SNP_ID_666048258 m1A Human chr19 + 41310302 41310302 41310302 GCGGGGCCCGCCGGGCGGTTGAAAAGTCCGAGAGAATCAGGATGGAGGCCGTGGCGACGGCGACG GCGGGGCCCGCCGGGCGGTTGAAAAGTCCGAGGGAATCAGGATGGAGGCCGTGGCGACGGCGACG A G CCDC97 Ensembl:ENSG00000142039 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41310252..41310375 26863196 MeRIP-seq:(Medium) rs945871524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1566287,Human_RBP_ID_4558480 Human_Splice_Rec_2011121 84548 RMVar_ID_84548 Human_SNP_ID_666051903 m1A Human chr19 - 41322977 41322960 41322978 GGGAGCGGGGGTAGGGAGAGAGACAGAAAGACAGAAAGAGACAGAAAGAAGCCCAGACAGACACC GGGAGCGGGGGTAGGGAGAGAGACAGAAAGA__________________AGCCCAGACAGACACC TTCTTTCTGTCTCTTTCTG T TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41322928..41322994 26863196 MeRIP-seq:(Medium) rs1240230427 Functional Loss DEL dbSNP153 32..49 33 - - - 84549 RMVar_ID_84549 Human_SNP_ID_666051906 m1A Human chr19 - 41322969 41322969 41322969 GGGTAGGGAGAGAGACAGAAAGACAGAAAGAGACAGAAAGAAGCCCAGACAGACACCAAGAAAGA GGGTAGGGAGAGAGACAGAAAGACAGAAAGAGGCAGAAAGAAGCCCAGACAGACACCAAGAAAGA T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41322919..41323480 26863196 MeRIP-seq:(Medium) rs1055854062 Functional Loss SNV dbSNP153 33..33 33 - - - 84550 RMVar_ID_84550 Human_SNP_ID_666052089 m1A Human chr19 + 41323596 41323596 41323596 ATCACGGGGCCTGCCAGCTTGAGTGTAGAGGGAGGGGGGACTCTACCCTTCTCAGCCCCACCAGC ATCACGGGGCCTGCCAGCTTGAGTGTAGAGGGTGGGGGGACTCTACCCTTCTCAGCCCCACCAGC A T CCDC97 Ensembl:ENSG00000142039 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41323549..41323707 26863196 MeRIP-seq:(Medium) rs1489515427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3572455,Human_RBP_ID_6766168,Human_RBP_ID_13461905,Human_RBP_ID_17081868,Human_RBP_ID_22503013 84551 RMVar_ID_84551 Human_SNP_ID_666052617 m1A Human chr19 - 41325434 41325434 41325434 GACAGAGCAGTGGCGGTGAGGGAGGAAGGCAGAGGGCTGGAAAGAAACGCACAGAAGCAGGGAGA GACAGAGCAGTGGCGGTGAGGGAGGAAGGCAGGGGGCTGGAAAGAAACGCACAGAAGCAGGGAGA T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41325323..41325494 26863196 MeRIP-seq:(Medium) rs1414871026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7717 84552 RMVar_ID_84552 Human_SNP_ID_666052618 m1A Human chr19 - 41325434 41325434 41325434 GACAGAGCAGTGGCGGTGAGGGAGGAAGGCAGAGGGCTGGAAAGAAACGCACAGAAGCAGGGAGA GACAGAGCAGTGGCGGTGAGGGAGGAAGGCAGCGGGCTGGAAAGAAACGCACAGAAGCAGGGAGA T G TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41325323..41325494 26863196 MeRIP-seq:(Medium) rs1414871026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7717 84553 RMVar_ID_84553 Human_SNP_ID_666054246 m1A Human chr19 + 41331123 41331123 41331123 CTGCTCCACCTTGGGCTTGCGGCCCACGTAGTACACGATGGGCAGCGGCTCCAGCGCCTGCGGCA CTGCTCCACCTTGGGCTTGCGGCCCACGTAGTGCACGATGGGCAGCGGCTCCAGCGCCTGCGGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41331072..41331146 26863196 MeRIP-seq:(Medium) rs1427369996 Functional Loss SNV dbSNP153 33..33 33 - - - 84554 RMVar_ID_84554 Human_SNP_ID_666054473 m1A Human chr19 - 41331799 41331798 41331800 AGAGACAAAATGAGAGAGACAGATACAGACACAGAGTTAGGCCAAGGAGAGACAAAGACAGATAC AGAGACAAAATGAGAGAGACAGATACAGACA__GAGTTAGGCCAAGGAGAGACAAAGACAGATAC CTG C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41331793..41331931 26863196 MeRIP-seq:(Medium) rs1331278063 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_7718 RMVar_hsa_circ_195011,RMVar_hsa_circ_105511 84555 RMVar_ID_84555 Human_SNP_ID_666057188 m1A Human chr19 + 41342028 41342028 41342028 GGTGGCCAGGTCACCTCGGCGGCCGGTAGTGAACCCTGCTTTGGTGTGGGAGTCAGGGGATAGGG GGTGGCCAGGTCACCTCGGCGGCCGGTAGTGATCCCTGCTTTGGTGTGGGAGTCAGGGGATAGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41331011..41342055 32194978 MeRIP-seq:(Medium) rs569594975 Functional Loss SNV dbSNP153 33..33 33 - - - 84556 RMVar_ID_84556 Human_SNP_ID_666060408 m1A Human chr19 - 41353410 41353409 41353411 GCCGACCCGGCCTCCCGCAAAGACTTTTCCCCAGACCTCGGGCGCACCCCCTGCACGCCGCCTTC GCCGACCCGGCCTCCCGCAAAGACTTTTCCC__GACCTCGGGCGCACCCCCTGCACGCCGCCTTC CTG C TGFB1 Ensembl:ENSG00000105329 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41353362..41353562 32194978 MeRIP-seq:(Medium) rs1491234345 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17386865,Human_RBP_ID_18192287,Human_RBP_ID_27468495,Human_RBP_ID_27562542 84557 RMVar_ID_84557 Human_SNP_ID_666060472 m1A Human chr19 + 41353655 41353655 41353655 GTCTCAAAAGTTTTTTTCCTCTTCTCCCGACCAGCTCGTCCCTCCTCCCGCTCCTCCTCCCCCTC GTCTCAAAAGTTTTTTTCCTCTTCTCCCGACCGGCTCGTCCCTCCTCCCGCTCCTCCTCCCCCTC A G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41353605..41353709 32194978 MeRIP-seq:(Medium) rs1448220113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566330,Human_RBP_ID_3583676 84558 RMVar_ID_84558 Human_SNP_ID_666063279 m1A Human chr19 - 41364027 41364024 41364027 AGCCAGGCCTGGTCGGCGCCCGCGGAGAAAAGAAGCAGTCAAGCCCATGAACTACAACCCCGGTT AGCCAGGCCTGGTCGGCGCCCGCGGAGAAAAG___CAGTCAAGCCCATGAACTACAACCCCGGTT GCTT G B9D2 Ensembl:ENSG00000123810 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41363976..41364150 26863196 MeRIP-seq:(Medium) rs1168437330 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4531412 Human_Splice_Rec_2011225,Human_Splice_Rec_2011231,Human_Splice_Rec_2011239 RMVar_hsa_circ_195021 84559 RMVar_ID_84559 Human_SNP_ID_666063291 m1A Human chr19 - 41364055 41364055 41364055 CAGCCAGGCGGGTCCTGGGAGAGGCGCGAGCCAGGCCTGGTCGGCGCCCGCGGAGAAAAGAAGCA CAGCCAGGCGGGTCCTGGGAGAGGCGCGAGCCCGGCCTGGTCGGCGCCCGCGGAGAAAAGAAGCA T G B9D2 Ensembl:ENSG00000123810 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41364004..41364130 26863196 MeRIP-seq:(Medium) rs1218548435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558491 Human_Splice_Rec_2011225,Human_Splice_Rec_2011231,Human_Splice_Rec_2011239 RMVar_hsa_circ_195021 84560 RMVar_ID_84560 Human_SNP_ID_666067049 m1A Human chr19 - 41377544 41377544 41377544 CAGGCCCAGGCACCCCTCCCAGTCACACACACACCCATCCCCTACCCCCAGTGCTGCCTGGAACT CAGGCCCAGGCACCCCTCCCAGTCACACACACGCCCATCCCCTACCCCCAGTGCTGCCTGGAACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41377507..41377689 26863196 MeRIP-seq:(Medium) rs760450848 Functional Loss SNV dbSNP153 33..33 33 - - - 84561 RMVar_ID_84561 Human_SNP_ID_666067299 m1A Human chr19 - 41378406 41378406 41378406 GGACTCGGCAAAGGCTATCTCTCTTAAGGGGGACCCCAGCTCATGCCTGCCAGGCTTCTGGGCAG GGACTCGGCAAAGGCTATCTCTCTTAAGGGGGGCCCCAGCTCATGCCTGCCAGGCTTCTGGGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41378283..41382985 32194978 MeRIP-seq:(Medium) rs1374888927 Functional Loss SNV dbSNP153 33..33 33 - - - 84562 RMVar_ID_84562 Human_SNP_ID_666067659 m1A Human chr19 + 41379554 41379550 41379554 GAAAGAAAGAAAAAGAGAGGGAGAGGGGGGAGAGAGAGAGAGAGAGAAAGAGAGAGGGAGGGAGG GAAAGAAAGAAAAAGAGAGGGAGAGGGGG____GAGAGAGAGAGAGAAAGAGAGAGGGAGGGAGG GGAGA G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41379548..41379668 26863196 MeRIP-seq:(Medium) rs904015109 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_22973445 RMVar_hsa_circ_322622 84563 RMVar_ID_84563 Human_SNP_ID_666067660 m1A Human chr19 + 41379554 41379550 41379554 GAAAGAAAGAAAAAGAGAGGGAGAGGGGGGAGAGAGAGAGAGAGAGAAAGAGAGAGGGAGGGAGG GAAAGAAAGAAAAAGAGAGGGAGAGGGGGGA__GAGAGAGAGAGAGAAAGAGAGAGGGAGGGAGG GGAGA GGA TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41379548..41379668 26863196 MeRIP-seq:(Medium) rs904015109 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22973445 RMVar_hsa_circ_322622 84564 RMVar_ID_84564 Human_SNP_ID_666080966 m1A Human chr19 + 41427890 41427889 41427890 AGGGTGAGGTGGGGGGAACGGGGCTGGTGAGGAGAAGGAGAGACAGAGACATTGTGGAGAGGGAA AGGGTGAGGTGGGGGGAACGGGGCTGGTGAGAGGAAGGAGAGACAGAGACATTGTGGAGAGGGAA GA AG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41427683..41428040 26863196 MeRIP-seq:(Medium) rs765936286 Functional Loss MNV dbSNP153 32..33 33 - - - 84565 RMVar_ID_84565 Human_SNP_ID_666082168 m1A Human chr19 + 41432310 41432310 41432310 CTGACTTCAGGCCCTCAGCCCAGTCGACTCCCACAACCTCGCAATTGGGCAGCATCTCCTCCACC CTGACTTCAGGCCCTCAGCCCAGTCGACTCCCCCAACCTCGCAATTGGGCAGCATCTCCTCCACC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41432213..41432313 32194978 MeRIP-seq:(Medium) rs1555769207 Functional Loss SNV dbSNP153 33..33 33 - - - 84566 RMVar_ID_84566 Human_SNP_ID_666082771 m1A Human chr19 - 41433335 41433335 41433335 CCGCCTCTACCCACTGGCCGACTCGTTGCAGGAGCTCTCGCTGGCCGGTTGCCCCCGCATCTCCG CCGCCTCTACCCACTGGCCGACTCGTTGCAGGGGCTCTCGCTGGCCGGTTGCCCCCGCATCTCCG T C DMAC2 Ensembl:ENSG00000105341 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:41433308..41433463 32194978 MeRIP-seq:(Medium) rs1555770053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137594 Human_Splice_Rec_2011362,Human_Splice_Rec_2011370,Human_Splice_Rec_2011371,Human_Splice_Rec_2011378,Human_Splice_Rec_2011379,Human_Splice_Rec_2011384,Human_Splice_Rec_2011385,Human_Splice_Rec_2011412,Human_Splice_Rec_2011413,Human_Splice_Rec_2011420,Human_Splice_Rec_2011424,Human_Splice_Rec_2011436,Human_Splice_Rec_2011444 RMVar_hsa_circ_104341,RMVar_hsa_circ_114588,RMVar_hsa_circ_126774,RMVar_hsa_circ_120294,RMVar_hsa_circ_104392,RMVar_hsa_circ_195038,RMVar_hsa_circ_195040,RMVar_hsa_circ_195041,RMVar_hsa_circ_195042,RMVar_hsa_circ_195039 84567 RMVar_ID_84567 Human_SNP_ID_666084197 m1A Human chr19 + 41438347 41438347 41438347 TCCTTTTCTTCTTCTGATTGCCCTCTGGGGCCACTGCCGCACCCAGGCGATGGATGCCCCTGATA TCCTTTTCTTCTTCTGATTGCCCTCTGGGGCCTCTGCCGCACCCAGGCGATGGATGCCCCTGATA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41438296..41438369 26863196 MeRIP-seq:(Medium) rs781958030 Functional Loss SNV dbSNP153 33..33 33 - - - 84568 RMVar_ID_84568 Human_SNP_ID_666084485 m1A Human chr19 - 41439313 41439313 41439313 AGATATTCTTTCAGAGGATTTAAAATCAAGGAATGAATTTAGGGAAAATTAAAGAGGTTGGCAGC AGATATTCTTTCAGAGGATTTAAAATCAAGGATTGAATTTAGGGAAAATTAAAGAGGTTGGCAGC T A DMAC2 Ensembl:ENSG00000105341 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41439308..41439873 26863196 MeRIP-seq:(Medium) rs1199083987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114588,RMVar_hsa_circ_195042 84569 RMVar_ID_84569 Human_SNP_ID_666193378 m1A Human chr19 + 41861162 41861162 41861162 CCCCGAATGGGTGGATACCGTCAAGCTGGCCAAGCACAAAGAGCTTGCTCCCTACGATGAGAACT CCCCGAATGGGTGGATACCGTCAAGCTGGCCACGCACAAAGAGCTTGCTCCCTACGATGAGAACT A C RPS19 Ensembl:ENSG00000105372 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41861067..41861264 26863196 MeRIP-seq:(Medium) rs199882057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239703,Human_RBP_ID_522587,Human_RBP_ID_1016409,Human_RBP_ID_1190200,Human_RBP_ID_1566358,Human_RBP_ID_1888514,Human_RBP_ID_3572527,Human_RBP_ID_4569388,Human_RBP_ID_8488610,Human_RBP_ID_9088207,Human_RBP_ID_13462773,Human_RBP_ID_17657098,Human_RBP_ID_18733848,Human_RBP_ID_22070239,Human_RBP_ID_22446806,Human_RBP_ID_23131395,Human_RBP_ID_23799109,Human_RBP_ID_26475011,Human_RBP_ID_26815929,Human_RBP_ID_27274882,Human_RBP_ID_27468531 Human_Splice_Rec_2012090,Human_Splice_Rec_2012094,Human_Splice_Rec_2012095,Human_Splice_Rec_2012100,Human_Splice_Rec_2012101,Human_Splice_Rec_2012110,Human_Splice_Rec_2012111,Human_Splice_Rec_2012120,Human_Splice_Rec_2012121,Human_Splice_Rec_2012130,Human_Splice_Rec_2012131,Human_Splice_Rec_2012136,Human_Splice_Rec_2012137,Human_Splice_Rec_2012144,Human_Splice_Rec_2012145 Human_miRNA_ID_2237789 RMVar_hsa_circ_292084 84570 RMVar_ID_84570 Human_SNP_ID_666194175 m1A Human chr19 + 41863645 41863645 41863645 CTTAATCCTGGGGTTTGGGGGTAAAGAGGCCCATGGTAGAAGATGGGGCCCTCTTGAGGGTGGTC CTTAATCCTGGGGTTTGGGGGTAAAGAGGCCCGTGGTAGAAGATGGGGCCCTCTTGAGGGTGGTC A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41863642..41863786 26863196 MeRIP-seq:(Medium) rs782009432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568634 84571 RMVar_ID_84571 Human_SNP_ID_666196124 m1A Human chr19 + 41869651 41869651 41869651 CTGGCTCACAGCCAGGAGGGAAGGGGCTGAGAACAGGACCTGTGCTCACTGGGGCCTGCATGACC CTGGCTCACAGCCAGGAGGGAAGGGGCTGAGACCAGGACCTGTGCTCACTGGGGCCTGCATGACC A C MIR6797,RPS19 Ensembl:ENSG00000276926,Ensembl:ENSG00000105372 miRNA,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41869648..41869780 26863196 MeRIP-seq:(Medium) rs1555841524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5261565,Human_RBP_ID_8488634,Human_RBP_ID_22503037 RMVar_hsa_circ_323257 84572 RMVar_ID_84572 Human_SNP_ID_666196181 m1A Human chr19 - 41869755 41869755 41869755 AGGGACCCAGCCCCACCCCAAACGCAGGCCTTACCTGTCCGGCGATTCTGTCCAGATCTCTTTGT AGGGACCCAGCCCCACCCCAAACGCAGGCCTTGCCTGTCCGGCGATTCTGTCCAGATCTCTTTGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:41869751..41869775 32194978 MeRIP-seq:(Medium) rs1555841598 Functional Loss SNV dbSNP153 33..33 33 - - - 84573 RMVar_ID_84573 Human_SNP_ID_666196922 m1A Human chr19 + 41871939 41871939 41871939 GGTAGAAAAGGACAGACCACCAGGGAGCCTCCACCGCAAACTGACCTGTGCTGCCTACACACTAA GGTAGAAAAGGACAGACCACCAGGGAGCCTCCCCCGCAAACTGACCTGTGCTGCCTACACACTAA A C RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41871888..41872037 32194978 MeRIP-seq:(Medium) rs1408200789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566434,Human_RBP_ID_8488659 84574 RMVar_ID_84574 Human_SNP_ID_666196923 m1A Human chr19 + 41871939 41871939 41871939 GGTAGAAAAGGACAGACCACCAGGGAGCCTCCACCGCAAACTGACCTGTGCTGCCTACACACTAA GGTAGAAAAGGACAGACCACCAGGGAGCCTCCTCCGCAAACTGACCTGTGCTGCCTACACACTAA A T RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41871888..41872037 32194978 MeRIP-seq:(Medium) rs1408200789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566434,Human_RBP_ID_8488659 84575 RMVar_ID_84575 Human_SNP_ID_666197207 m1A Human chr19 + 41872774 41872774 41872774 AAAATTAGTTGGGCATGGTGGCGCGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAAGA AAAATTAGTTGGGCATGGTGGCGCGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGAAGA A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1555842289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566438,Human_RBP_ID_26468576 84576 RMVar_ID_84576 Human_SNP_ID_666200378 m1A Human chr19 - 41884023 41884023 41884023 GGGACCCGCTGAATTTCCAATCCTCGTACATCAATCCCCTCCGTCTCCCACCCCCAGCCCCTTCC GGGACCCGCTGAATTTCCAATCCTCGTACATCGATCCCCTCCGTCTCCCACCCCCAGCCCCTTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41884016..41884544 26863196 MeRIP-seq:(Medium) rs1372363424 Functional Loss SNV dbSNP153 33..33 33 - - - 84577 RMVar_ID_84577 Human_SNP_ID_666202329 m1A Human chr19 + 41891921 41891921 41891921 GTGCTTCCCAGAGGAAGTGGCAGTTGAGTCCCACAGCCATAGGATGGCCAGGAGGTGAGGAAGGC GTGCTTCCCAGAGGAAGTGGCAGTTGAGTCCCCCAGCCATAGGATGGCCAGGAGGTGAGGAAGGC A C ARHGEF1 Ensembl:ENSG00000076928 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:41891918..41892042 26863196 MeRIP-seq:(Medium) rs1385838802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17670245,Human_RBP_ID_18412543 84578 RMVar_ID_84578 Human_SNP_ID_666202565 m1A Human chr19 + 41892639 41892639 41892639 CACTAGGGCTGACCTCATCTCCGAGGATGTCCAGCGGCGGTTCGTGCAGGAGGTGGTGCAAAGCC CACTAGGGCTGACCTCATCTCCGAGGATGTCCCGCGGCGGTTCGTGCAGGAGGTGGTGCAAAGCC A C ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41892635..41893225 32194978 MeRIP-seq:(Medium) rs782320477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_909622,Human_RBP_ID_3957021,Human_RBP_ID_5469606,Human_RBP_ID_8839376,Human_RBP_ID_9293763,Human_RBP_ID_9382579,Human_RBP_ID_18995012,Human_RBP_ID_27815464 Human_Splice_Rec_2012186,Human_Splice_Rec_2012242,Human_Splice_Rec_2012300,Human_Splice_Rec_2012356,Human_Splice_Rec_2012410,Human_Splice_Rec_2012464 84579 RMVar_ID_84579 Human_SNP_ID_666202619 m1A Human chr19 - 41892767 41892767 41892767 GGCCTCGTAGCTGGCTCGGTCCCGCCCAACCCAAGCCTCCAGCTGGGCCAGCTCCTGCTCCCAGG GGCCTCGTAGCTGGCTCGGTCCCGCCCAACCCGAGCCTCCAGCTGGGCCAGCTCCTGCTCCCAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41892717..41892888 26863196 MeRIP-seq:(Medium) rs1555846542 Functional Loss SNV dbSNP153 33..33 33 - - - 84580 RMVar_ID_84580 Human_SNP_ID_666203282 m1A Human chr19 + 41894301 41894300 41894301 GAGACAAGAAGTCGGGGAGGAACTTCTTCCGGAAAAAGGTGCTTCCCTCAGTGCCCCGTCCTGAC GAGACAAGAAGTCGGGGAGGAACTTCTTCCGG_AAAAGGTGCTTCCCTCAGTGCCCCGTCCTGAC GA G ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41894251..41894440 26863196 MeRIP-seq:(Medium) rs781910454 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2012190,Human_Splice_Rec_2012191,Human_Splice_Rec_2012246,Human_Splice_Rec_2012247,Human_Splice_Rec_2012304,Human_Splice_Rec_2012305,Human_Splice_Rec_2012360,Human_Splice_Rec_2012361,Human_Splice_Rec_2012414,Human_Splice_Rec_2012415,Human_Splice_Rec_2012468,Human_Splice_Rec_2012469,Human_Splice_Rec_2012512,Human_Splice_Rec_2012513,Human_Splice_Rec_2012519 RMVar_hsa_circ_20405,RMVar_hsa_circ_376999 84581 RMVar_ID_84581 Human_SNP_ID_666203332 m1A Human chr19 + 41894460 41894460 41894460 TCTTCCTCCCCGCCCTCTCACAGGTGATGGGGAACCGGCGGTCGGACGAGCCTGCCAAGACCAAG TCTTCCTCCCCGCCCTCTCACAGGTGATGGGGTACCGGCGGTCGGACGAGCCTGCCAAGACCAAG A T ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41894451..41894550 26863196 MeRIP-seq:(Medium) rs1555847072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824390,Human_RBP_ID_3955114,Human_RBP_ID_9293765,Human_RBP_ID_9381072,Human_RBP_ID_17935420,Human_RBP_ID_18995015 Human_Splice_Rec_2012192,Human_Splice_Rec_2012193,Human_Splice_Rec_2012248,Human_Splice_Rec_2012249,Human_Splice_Rec_2012306,Human_Splice_Rec_2012307,Human_Splice_Rec_2012362,Human_Splice_Rec_2012363,Human_Splice_Rec_2012416,Human_Splice_Rec_2012417,Human_Splice_Rec_2012470,Human_Splice_Rec_2012471,Human_Splice_Rec_2012514,Human_Splice_Rec_2012515,Human_Splice_Rec_2012520,Human_Splice_Rec_2012521,Human_Splice_Rec_2012533 RMVar_hsa_circ_20405,RMVar_hsa_circ_376999 84582 RMVar_ID_84582 Human_SNP_ID_666203338 m1A Human chr19 - 41894469 41894469 41894469 CAGCCCCTTCTTGGTCTTGGCAGGCTCGTCCGACCGCCGGTTCCCCATCACCTGTGAGAGGGCGG CAGCCCCTTCTTGGTCTTGGCAGGCTCGTCCGCCCGCCGGTTCCCCATCACCTGTGAGAGGGCGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:41894276..41894525 26863196 MeRIP-seq:(Medium) rs782545099 Functional Loss SNV dbSNP153 33..33 33 - - - 84583 RMVar_ID_84583 Human_SNP_ID_666204602 m1A Human chr19 + 41897584 41897584 41897584 TCCATCCTGGGTTCCCCATCCCTTCCCCCATCAAATTTCAGTATCCCCCCTCCCCCAAGACCCCC TCCATCCTGGGTTCCCCATCCCTTCCCCCATCCAATTTCAGTATCCCCCCTCCCCCAAGACCCCC A C ARHGEF1 Ensembl:ENSG00000076928 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41897579..41897868 26863196 MeRIP-seq:(Medium) rs1555848111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131264,Human_RBP_ID_17081879 84584 RMVar_ID_84584 Human_SNP_ID_666205803 m1A Human chr19 + 41901950 41901950 41901950 CATGCTGCGGGTGCTGCACGACCTCTTCTTCCAGCCCATGGCAGAATGCCTGTTCTTCCCCTTGG CATGCTGCGGGTGCTGCACGACCTCTTCTTCCTGCCCATGGCAGAATGCCTGTTCTTCCCCTTGG A T ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41901901..41902000 32194978 MeRIP-seq:(Medium) rs781999337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2012202,Human_Splice_Rec_2012203,Human_Splice_Rec_2012260,Human_Splice_Rec_2012261,Human_Splice_Rec_2012316,Human_Splice_Rec_2012317,Human_Splice_Rec_2012372,Human_Splice_Rec_2012373,Human_Splice_Rec_2012426,Human_Splice_Rec_2012427,Human_Splice_Rec_2012480,Human_Splice_Rec_2012481,Human_Splice_Rec_2012532,Human_Splice_Rec_2012548,Human_Splice_Rec_2012549,Human_Splice_Rec_2012580,Human_Splice_Rec_2012581,Human_Splice_Rec_2012612,Human_Splice_Rec_2012613,Human_Splice_Rec_2012622,Human_Splice_Rec_2012623 84585 RMVar_ID_84585 Human_SNP_ID_666207036 m1A Human chr19 + 41905718 41905718 41905718 AGCTCTCTGTCTCCCTGCCCCTGCGGCCCCCCAGGGCCAGGGGTGTGGGGTCACCCAGCACTTCC AGCTCTCTGTCTCCCTGCCCCTGCGGCCCCCCGGGGCCAGGGGTGTGGGGTCACCCAGCACTTCC A G ARHGEF1 Ensembl:ENSG00000076928 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41905712..41906073 32194978 MeRIP-seq:(Medium) rs1555850001 Functional Loss SNV dbSNP153 33..33 33 - - - 84586 RMVar_ID_84586 Human_SNP_ID_666207139 m1A Human chr19 + 41905985 41905985 41905985 ATCCTCAGTGACCTCCTGCCCTTCTGCAGACCAGGCCCCGAGGGCCAGCTCGCTGCCACGGCCCT ATCCTCAGTGACCTCCTGCCCTTCTGCAGACCGGGCCCCGAGGGCCAGCTCGCTGCCACGGCCCT A G ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:41905826..41906000 26863196 MeRIP-seq:(Medium) rs782189573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_907804,Human_RBP_ID_8839386,Human_RBP_ID_9293780,Human_RBP_ID_9381080,Human_RBP_ID_18995030 Human_Splice_Rec_2012224,Human_Splice_Rec_2012225,Human_Splice_Rec_2012282,Human_Splice_Rec_2012283,Human_Splice_Rec_2012338,Human_Splice_Rec_2012339,Human_Splice_Rec_2012394,Human_Splice_Rec_2012395,Human_Splice_Rec_2012448,Human_Splice_Rec_2012449,Human_Splice_Rec_2012502,Human_Splice_Rec_2012503,Human_Splice_Rec_2012570,Human_Splice_Rec_2012571,Human_Splice_Rec_2012602,Human_Splice_Rec_2012603,Human_Splice_Rec_2012644,Human_Splice_Rec_2012645,Human_Splice_Rec_2012652,Human_Splice_Rec_2012654,Human_Splice_Rec_2012656 84587 RMVar_ID_84587 Human_SNP_ID_666222058 m1A Human chr19 - 41958850 41958850 41958850 CATCCGGCCCTGGAGCACCTTCGTGGACCAGCAGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC CATCCGGCCCTGGAGCACCTTCGTGGACCAGCGGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:41958801..41958989;chr19:41958801..41958990 26863196 MeRIP-seq:(Medium) rs112970995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_522641,Human_RBP_ID_1566407,Human_RBP_ID_8488705,Human_RBP_ID_9088231,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_3066403 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84588 RMVar_ID_84588 Human_SNP_ID_666222059 m1A Human chr19 - 41958850 41958850 41958850 CATCCGGCCCTGGAGCACCTTCGTGGACCAGCAGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC CATCCGGCCCTGGAGCACCTTCGTGGACCAGCCGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC T G RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:41958801..41958989;chr19:41958801..41958990 26863196 MeRIP-seq:(Medium) rs112970995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_522641,Human_RBP_ID_1566407,Human_RBP_ID_8488705,Human_RBP_ID_9088231,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_3066403 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84589 RMVar_ID_84589 Human_SNP_ID_666222061 m1A Human chr19 - 41958853 41958853 41958853 GACCATCCGGCCCTGGAGCACCTTCGTGGACCAGCAGCGCTTCTCACGGCCCCGCAACCTGGGAG GACCATCCGGCCCTGGAGCACCTTCGTGGACCGGCAGCGCTTCTCACGGCCCCGCAACCTGGGAG T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:41958288..41958990 32194978 MeRIP-seq:(Medium) rs1370394555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_1566407,Human_RBP_ID_8488705,Human_RBP_ID_9088231,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84590 RMVar_ID_84590 Human_SNP_ID_666222075 m1A Human chr19 - 41958884 41958884 41958884 CAGGCCGGGAGTGGCTGGAGCGGCGCCGCGCGACCATCCGGCCCTGGAGCACCTTCGTGGACCAG CAGGCCGGGAGTGGCTGGAGCGGCGCCGCGCGTCCATCCGGCCCTGGAGCACCTTCGTGGACCAG T A RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41958723..41958994 26863196 MeRIP-seq:(Medium) rs782792807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_238920,Human_RBP_ID_522642,Human_RBP_ID_769621,Human_RBP_ID_4557522,Human_RBP_ID_5116921,Human_RBP_ID_17925972,Human_RBP_ID_22447786,Human_RBP_ID_26990714 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_1957727,Human_miRNA_ID_2575050 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84591 RMVar_ID_84591 Human_SNP_ID_666222080 m1A Human chr19 - 41958898 41958897 41958898 GATTCCCTCCGGTGCAGGCCGGGAGTGGCTGGAGCGGCGCCGCGCGACCATCCGGCCCTGGAGCA GATTCCCTCCGGTGCAGGCCGGGAGTGGCTGG_GCGGCGCCGCGCGACCATCCGGCCCTGGAGCA CT C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:41958776..41959000 26863410 MeRIP-seq:(Medium) rs1555857231 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_238920,Human_RBP_ID_522643,Human_RBP_ID_769621,Human_RBP_ID_914617,Human_RBP_ID_4557522,Human_RBP_ID_5116921,Human_RBP_ID_17925973,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_1957727,Human_miRNA_ID_2975044,Human_miRNA_ID_3008241 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84592 RMVar_ID_84592 Human_SNP_ID_666222081 m1A Human chr19 - 41958898 41958898 41958898 GATTCCCTCCGGTGCAGGCCGGGAGTGGCTGGAGCGGCGCCGCGCGACCATCCGGCCCTGGAGCA GATTCCCTCCGGTGCAGGCCGGGAGTGGCTGGGGCGGCGCCGCGCGACCATCCGGCCCTGGAGCA T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:41958776..41959000 26863410 MeRIP-seq:(Medium) rs201138159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137626,Human_RBP_ID_238920,Human_RBP_ID_522643,Human_RBP_ID_769621,Human_RBP_ID_914617,Human_RBP_ID_4557522,Human_RBP_ID_5116921,Human_RBP_ID_17925973,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_1957727,Human_miRNA_ID_2975044,Human_miRNA_ID_3008241 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84593 RMVar_ID_84593 Human_SNP_ID_666222257 m1A Human chr19 - 41959287 41959287 41959287 AGCAGCTCTACCCCTCACGACGCAGACATGGCAGCGCAGAAGGACCAGCAGAAAGATGCCGAGGC AGCAGCTCTACCCCTCACGACGCAGACATGGCGGCGCAGAAGGACCAGCAGAAAGATGCCGAGGC T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:41959189..41959350;chr19:41959197..41959375;chr19:41959188..41959375;chr19:41959187..41959350 26863196 MeRIP-seq:(Medium) rs1555857382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116922 Human_Splice_Rec_2012677,Human_Splice_Rec_2012685,Human_Splice_Rec_2012691,Human_Splice_Rec_2012717 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84594 RMVar_ID_84594 Human_SNP_ID_666222258 m1A Human chr19 - 41959287 41959287 41959287 AGCAGCTCTACCCCTCACGACGCAGACATGGCAGCGCAGAAGGACCAGCAGAAAGATGCCGAGGC AGCAGCTCTACCCCTCACGACGCAGACATGGCCGCGCAGAAGGACCAGCAGAAAGATGCCGAGGC T G RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:41959189..41959350;chr19:41959197..41959375;chr19:41959188..41959375;chr19:41959187..41959350 26863196 MeRIP-seq:(Medium) rs1555857382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116922 Human_Splice_Rec_2012677,Human_Splice_Rec_2012685,Human_Splice_Rec_2012691,Human_Splice_Rec_2012717 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84595 RMVar_ID_84595 Human_SNP_ID_666222267 m1A Human chr19 - 41959300 41959300 41959300 CCGGGCTGGTTACAGCAGCTCTACCCCTCACGACGCAGACATGGCAGCGCAGAAGGACCAGCAGA CCGGGCTGGTTACAGCAGCTCTACCCCTCACGGCGCAGACATGGCAGCGCAGAAGGACCAGCAGA T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:41959251..41959325 26863196 MeRIP-seq:(Medium) rs782499764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558506,Human_RBP_ID_5116922,Human_RBP_ID_26990717 Human_Splice_Rec_2012677,Human_Splice_Rec_2012685,Human_Splice_Rec_2012691,Human_Splice_Rec_2012717 Human_miRNA_ID_2979950 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 84596 RMVar_ID_84596 Human_SNP_ID_666252268 m1A Human chr19 + 42075708 42075708 42075708 CTCGGGGAAACCACAAAGGTTCCCGTGCCTCCATTCCCCCGCTCCAGCCCTCAAGGTGCCGCGTG CTCGGGGAAACCACAAAGGTTCCCGTGCCTCCGTTCCCCCGCTCCAGCCCTCAAGGTGCCGCGTG A G ZNF574 Ensembl:ENSG00000105732 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:42075685..42075798 26863196 MeRIP-seq:(Medium) rs560498788 Functional Loss SNV dbSNP153 33..33 33 - - - 84597 RMVar_ID_84597 Human_SNP_ID_666252458 m1A Human chr19 + 42076190 42076190 42076190 CTGGGGGCGAGAGCGAGGCTACGGAGCAGGCGAGAGGCGACGGCGAGAGCTAGAGCGGGCGCAGC CTGGGGGCGAGAGCGAGGCTACGGAGCAGGCGGGAGGCGACGGCGAGAGCTAGAGCGGGCGCAGC A G ZNF574 Ensembl:ENSG00000105732 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:42076139..42078625;chr19:42076126..42078621 26863196 MeRIP-seq:(Medium) rs1024601443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4531886,Human_RBP_ID_18421388 Human_Splice_Rec_2013189 84598 RMVar_ID_84598 Human_SNP_ID_666252462 m1A Human chr19 + 42076197 42076197 42076197 CGAGAGCGAGGCTACGGAGCAGGCGAGAGGCGACGGCGAGAGCTAGAGCGGGCGCAGCGTTAGGG CGAGAGCGAGGCTACGGAGCAGGCGAGAGGCGGCGGCGAGAGCTAGAGCGGGCGCAGCGTTAGGG A G ZNF574 Ensembl:ENSG00000105732 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42076151..42076300 26863196 MeRIP-seq:(Medium) rs1041110636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4531886,Human_RBP_ID_18421388 Human_Splice_Rec_2013189 84599 RMVar_ID_84599 Human_SNP_ID_666253111 m1A Human chr19 - 42078515 42078515 42078515 CGATTCCTCAGCTCTTCCCTTCATCACTCTCCACTCCTAATACCTTAGATCTACACCCCCTTAAG CGATTCCTCAGCTCTTCCCTTCATCACTCTCCTCTCCTAATACCTTAGATCTACACCCCCTTAAG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42078514..42078634 26863196 MeRIP-seq:(Medium) rs1423769430 Functional Loss SNV dbSNP153 33..33 33 - - - 84600 RMVar_ID_84600 Human_SNP_ID_666253170 m1A Human chr19 + 42078671 42078671 42078671 CATTGAGCACCGCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTTA CATTGAGCACCGCTATGTCTGCTCTGAGTGCACCCAGCTGTATGGATCACTGGAAGAGGTGCTTA A C ZNF574 Ensembl:ENSG00000105732 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42076221..42078671 32194978 MeRIP-seq:(Medium) rs1391219080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1566412,Human_RBP_ID_1888568,Human_RBP_ID_18733915,Human_RBP_ID_21892745,Human_RBP_ID_23799316 Human_Splice_Rec_2013182,Human_Splice_Rec_2013184,Human_Splice_Rec_2013188,Human_Splice_Rec_2013190 84601 RMVar_ID_84601 Human_SNP_ID_666253171 m1A Human chr19 + 42078671 42078671 42078671 CATTGAGCACCGCTATGTCTGCTCTGAGTGCAACCAGCTGTATGGATCACTGGAAGAGGTGCTTA CATTGAGCACCGCTATGTCTGCTCTGAGTGCAGCCAGCTGTATGGATCACTGGAAGAGGTGCTTA A G ZNF574 Ensembl:ENSG00000105732 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42076221..42078671 32194978 MeRIP-seq:(Medium) rs1391219080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1566412,Human_RBP_ID_1888568,Human_RBP_ID_18733915,Human_RBP_ID_21892745,Human_RBP_ID_23799316 Human_Splice_Rec_2013182,Human_Splice_Rec_2013184,Human_Splice_Rec_2013188,Human_Splice_Rec_2013190 84602 RMVar_ID_84602 Human_SNP_ID_666262990 m1A Human chr19 + 42116793 42116791 42116794 GGCTGGCTGGCAGGCTGTGGTGGTGGCAGGTCACCCCCCCCAGAGGAGGCTGGGGGCTGTGAGGT GGCTGGCTGGCAGGCTGTGGTGGTGGCAGGT___CCCCCCCAGAGGAGGCTGGGGGCTGTGAGGT TCAC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42116776..42116825 26863196 MeRIP-seq:(Medium) rs1345629246 Functional Loss DEL dbSNP153 32..34 33 - - - 84603 RMVar_ID_84603 Human_SNP_ID_666276697 m1A Human chr19 + 42177056 42177052 42177056 GGGCGGGCAGGGGCTGCGAGGGGAGAGGGAGGAAGGGAGGGCAGGCGGGCGGGCGCGCAGGCGAG GGGCGGGCAGGGGCTGCGAGGGGAGAGGG____AGGGAGGGCAGGCGGGCGGGCGCGCAGGCGAG GAGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42177051..42177100 26863196 MeRIP-seq:(Medium) rs1051615367 Functional Loss DEL dbSNP153 30..33 33 - - - 84604 RMVar_ID_84604 Human_SNP_ID_666276699 m1A Human chr19 + 42177056 42177056 42177056 GGGCGGGCAGGGGCTGCGAGGGGAGAGGGAGGAAGGGAGGGCAGGCGGGCGGGCGCGCAGGCGAG GGGCGGGCAGGGGCTGCGAGGGGAGAGGGAGGGAGGGAGGGCAGGCGGGCGGGCGCGCAGGCGAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42177051..42177100 26863196 MeRIP-seq:(Medium) rs888983153 Functional Loss SNV dbSNP153 33..33 33 - - - 84605 RMVar_ID_84605 Human_SNP_ID_666282379 m1A Human chr19 - 42199413 42199413 42199413 CCTCCTGATCCAGGACTGGCAGGATTGATCCCACCTCCAAGTCTCCGGGCCACCTTCTCCTGGGA CCTCCTGATCCAGGACTGGCAGGATTGATCCCCCCTCCAAGTCTCCGGGCCACCTTCTCCTGGGA T G DEDD2 Ensembl:ENSG00000160570 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42199363..42199604 26863196 MeRIP-seq:(Medium) rs1359187795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116924,Human_RBP_ID_17926046,Human_RBP_ID_22070256,Human_RBP_ID_26472571,Human_RBP_ID_27468608 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84606 RMVar_ID_84606 Human_SNP_ID_666282384 m1A Human chr19 - 42199422 42199422 42199422 CGACAGAGGCCTCCTGATCCAGGACTGGCAGGATTGATCCCACCTCCAAGTCTCCGGGCCACCTT CGACAGAGGCCTCCTGATCCAGGACTGGCAGGGTTGATCCCACCTCCAAGTCTCCGGGCCACCTT T C DEDD2 Ensembl:ENSG00000160570 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42199412..42199577 26863196 MeRIP-seq:(Medium) rs1200118252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4532038,Human_RBP_ID_5116924 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84607 RMVar_ID_84607 Human_SNP_ID_666282398 m1A Human chr19 - 42199452 42199452 42199452 TGCTGATGGAGGAGGAAGGGGGGCGGCGCCCGACAGAGGCCTCCTGATCCAGGACTGGCAGGATT TGCTGATGGAGGAGGAAGGGGGGCGGCGCCCGGCAGAGGCCTCCTGATCCAGGACTGGCAGGATT T C DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:42199451..42199475 26863196 MeRIP-seq:(Medium) rs1246627165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771841,Human_RBP_ID_4532039,Human_RBP_ID_22067212,Human_RBP_ID_26472572 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84608 RMVar_ID_84608 Human_SNP_ID_666282411 m1A Human chr19 - 42199468 42199468 42199468 GGCCGGCGCCGCCTGTTGCTGATGGAGGAGGAAGGGGGGCGGCGCCCGACAGAGGCCTCCTGATC GGCCGGCGCCGCCTGTTGCTGATGGAGGAGGAGGGGGGGCGGCGCCCGACAGAGGCCTCCTGATC T C DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42199451..42199525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4532039,Human_RBP_ID_22070257,Human_RBP_ID_26472572,Human_RBP_ID_27468611 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84609 RMVar_ID_84609 Human_SNP_ID_666282551 m1A Human chr19 + 42199854 42199854 42199854 CCGGATGTCTGCAGGGGAAGGAGGGATTTGTCAGGGAGGGGGCCAACACTAGACACACTTATGGG CCGGATGTCTGCAGGGGAAGGAGGGATTTGTCGGGGAGGGGGCCAACACTAGACACACTTATGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42199851..42199900 26863196 MeRIP-seq:(Medium) rs1307836867 Functional Loss SNV dbSNP153 33..33 33 - - - 84610 RMVar_ID_84610 Human_SNP_ID_666282552 m1A Human chr19 + 42199854 42199854 42199854 CCGGATGTCTGCAGGGGAAGGAGGGATTTGTCAGGGAGGGGGCCAACACTAGACACACTTATGGG CCGGATGTCTGCAGGGGAAGGAGGGATTTGTCTGGGAGGGGGCCAACACTAGACACACTTATGGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42199851..42199900 26863196 MeRIP-seq:(Medium) rs1307836867 Functional Loss SNV dbSNP153 33..33 33 - - - 84611 RMVar_ID_84611 Human_SNP_ID_666284595 m1A Human chr19 - 42208321 42208318 42208321 TGGAGAGGGTGAGGAGAAGTGACCTAGGAAATAAGGAAGGGCACTGGCCATAGGGCTGACTGTAG TGGAGAGGGTGAGGAGAAGTGACCTAGGAAAT___GAAGGGCACTGGCCATAGGGCTGACTGTAG CCTT C DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42208316..42208429 26863196 MeRIP-seq:(Medium) rs949692423 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84612 RMVar_ID_84612 Human_SNP_ID_666285017 m1A Human chr19 - 42209829 42209829 42209829 GCCCCATTTTTTTCCCCTCAGGCTCCCCCCCAACCAAGCGGCAGCGGCGGAGTCGGGGCCGGCCC GCCCCATTTTTTTCCCCTCAGGCTCCCCCCCAGCCAAGCGGCAGCGGCGGAGTCGGGGCCGGCCC T C DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:42209747..42209850;chr19:42209779..42209893 26863410,26863196 MeRIP-seq:(Medium) rs1431014334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18997949,Human_RBP_ID_22662749 Human_Splice_Rec_2013546,Human_Splice_Rec_2013554,Human_Splice_Rec_2013562,Human_Splice_Rec_2013568,Human_Splice_Rec_2013574,Human_Splice_Rec_2013582,Human_Splice_Rec_2013598,Human_Splice_Rec_2013604,Human_Splice_Rec_2013614,Human_Splice_Rec_2013620,Human_Splice_Rec_2013626 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84613 RMVar_ID_84613 Human_SNP_ID_666285018 m1A Human chr19 - 42209829 42209829 42209829 GCCCCATTTTTTTCCCCTCAGGCTCCCCCCCAACCAAGCGGCAGCGGCGGAGTCGGGGCCGGCCC GCCCCATTTTTTTCCCCTCAGGCTCCCCCCCACCCAAGCGGCAGCGGCGGAGTCGGGGCCGGCCC T G DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:42209747..42209850;chr19:42209779..42209893 26863410,26863196 MeRIP-seq:(Medium) rs1431014334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18997949,Human_RBP_ID_22662749 Human_Splice_Rec_2013546,Human_Splice_Rec_2013554,Human_Splice_Rec_2013562,Human_Splice_Rec_2013568,Human_Splice_Rec_2013574,Human_Splice_Rec_2013582,Human_Splice_Rec_2013598,Human_Splice_Rec_2013604,Human_Splice_Rec_2013614,Human_Splice_Rec_2013620,Human_Splice_Rec_2013626 RMVar_hsa_circ_104137,RMVar_hsa_circ_195073 84614 RMVar_ID_84614 Human_SNP_ID_666286700 m1A Human chr19 - 42215937 42215936 42215937 GGTAAGAAGTTATGTCATGAAGGGGCTTGCAGAGAACGTAGCTGGGAAGTGTGGGAGCCAGGATT GGTAAGAAGTTATGTCATGAAGGGGCTTGCAG_GAACGTAGCTGGGAAGTGTGGGAGCCAGGATT CT C DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42215934..42216118 26863196 MeRIP-seq:(Medium) rs1249809723 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13463508 84615 RMVar_ID_84615 Human_SNP_ID_666287008 m1A Human chr19 + 42216919 42216919 42216919 CGCACTCGGTCAGTTGCCCGCCCACCACCTCGAACATACGGTGAAGCGACAGCATCCCGTAGTAG CGCACTCGGTCAGTTGCCCGCCCACCACCTCGTACATACGGTGAAGCGACAGCATCCCGTAGTAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42216916..42217025 26863196 MeRIP-seq:(Medium) rs34087334 Functional Loss SNV dbSNP153 33..33 33 - - - 84616 RMVar_ID_84616 Human_SNP_ID_666287011 m1A Human chr19 - 42216923 42216923 42216923 TGGACTACTACGGGATGCTGTCGCTTCACCGTATGTTCGAGGTGGTGGGCGGGCAACTGACCGAG TGGACTACTACGGGATGCTGTCGCTTCACCGTTTGTTCGAGGTGGTGGGCGGGCAACTGACCGAG T A DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42215189..42217014 32194978 MeRIP-seq:(Medium) rs373486854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4532072,Human_RBP_ID_27274965 84617 RMVar_ID_84617 Human_SNP_ID_666287012 m1A Human chr19 - 42216923 42216923 42216923 TGGACTACTACGGGATGCTGTCGCTTCACCGTATGTTCGAGGTGGTGGGCGGGCAACTGACCGAG TGGACTACTACGGGATGCTGTCGCTTCACCGTGTGTTCGAGGTGGTGGGCGGGCAACTGACCGAG T C DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42215189..42217014 32194978 MeRIP-seq:(Medium) rs373486854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4532072,Human_RBP_ID_27274965 84618 RMVar_ID_84618 Human_SNP_ID_666287013 m1A Human chr19 - 42216923 42216923 42216923 TGGACTACTACGGGATGCTGTCGCTTCACCGTATGTTCGAGGTGGTGGGCGGGCAACTGACCGAG TGGACTACTACGGGATGCTGTCGCTTCACCGTCTGTTCGAGGTGGTGGGCGGGCAACTGACCGAG T G DEDD2 Ensembl:ENSG00000160570 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42215189..42217014 32194978 MeRIP-seq:(Medium) rs373486854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4532072,Human_RBP_ID_27274965 84619 RMVar_ID_84619 Human_SNP_ID_666287127 m1A Human chr19 - 42217175 42217174 42217175 CGGGCGGGACCATTCCCTCCCGGGGGAGGGGGAGGCCGAGGCGGTTGGGGGTGCGGGAGCGGCCC CGGGCGGGACCATTCCCTCCCGGGGGAGGGGG_GGCCGAGGCGGTTGGGGGTGCGGGAGCGGCCC CT C DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42217168..42217725 26863196 MeRIP-seq:(Medium) rs1011972666 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3583694,Human_RBP_ID_8196537,Human_RBP_ID_8728071 84620 RMVar_ID_84620 Human_SNP_ID_666287298 m1A Human chr19 - 42217682 42217682 42217682 GCGTAATAATAGAGAAGGTGCCAGAAAGATCCAAAACAAGTGGCTGCGGCCGTCGCCCAGGAGTC GCGTAATAATAGAGAAGGTGCCAGAAAGATCCGAAACAAGTGGCTGCGGCCGTCGCCCAGGAGTC T C DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42217387..42217795 26863196 MeRIP-seq:(Medium) rs1358942582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2013541,Human_Splice_Rec_2013549,Human_Splice_Rec_2013565,Human_Splice_Rec_2013571,Human_Splice_Rec_2013579,Human_Splice_Rec_2013587,Human_Splice_Rec_2013595,Human_Splice_Rec_2013601,Human_Splice_Rec_2013609,Human_Splice_Rec_2013623,Human_Splice_Rec_2013629 84621 RMVar_ID_84621 Human_SNP_ID_666289027 m1A Human chr19 - 42224192 42224192 42224192 CCACGGCAGCCTGCAGGAGAGAAACACCACTCAGCCCAGCCTCTTTTTTTTTTTTTTTTTTCTTC CCACGGCAGCCTGCAGGAGAGAAACACCACTCGGCCCAGCCTCTTTTTTTTTTTTTTTTTTCTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:42224190..42224300;chr19:42224188..42224441 26863196 MeRIP-seq:(Medium) rs555378117 Functional Loss SNV dbSNP153 33..33 33 - - - 84622 RMVar_ID_84622 Human_SNP_ID_666289347 m1A Human chr19 - 42225153 42225150 42225153 GCATCATCACCGACCTCTGCCATGGCCTCCTCATCCTCCATCTCTTCATCATCTTCTTCATCCTC GCATCATCACCGACCTCTGCCATGGCCTCCTC___CTCCATCTCTTCATCATCTTCTTCATCCTC GGAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42225046..42225212 26863196 MeRIP-seq:(Medium) rs587780524 Functional Loss DEL dbSNP153 33..35 33 - - - 84623 RMVar_ID_84623 Human_SNP_ID_666290850 m1A Human chr19 - 42230244 42230244 42230244 GAGTGGAGAGAGCTCCTGATGTCTTAGTTTCCACAGTAAGGTTTGCCTGTGTACAGACCTCCGTT GAGTGGAGAGAGCTCCTGATGTCTTAGTTTCCCCAGTAAGGTTTGCCTGTGTACAGACCTCCGTT T G GSK3A Ensembl:ENSG00000105723 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42230232..42230475 26863196 MeRIP-seq:(Medium) rs1054371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53453,Human_RBP_ID_522686,Human_RBP_ID_1566430,Human_RBP_ID_1888576,Human_RBP_ID_4532152,Human_RBP_ID_8488747,Human_RBP_ID_9088254,Human_RBP_ID_17272153,Human_RBP_ID_17568651,Human_RBP_ID_18946935,Human_RBP_ID_23799373,Human_RBP_ID_26474046 RMVar_hsa_circ_110054,RMVar_hsa_circ_195075,RMVar_hsa_circ_93168,RMVar_hsa_circ_195074 84624 RMVar_ID_84624 Human_SNP_ID_666290983 m1A Human chr19 - 42230687 42230687 42230687 AAGCTCCTGCCCTGGCTGGGCCCCTAGACTAGAGGGCAGAGGTAAATGAGTCCCTGTCCCCACCT AAGCTCCTGCCCTGGCTGGGCCCCTAGACTAGTGGGCAGAGGTAAATGAGTCCCTGTCCCCACCT T A GSK3A Ensembl:ENSG00000105723 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs924007280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522706,Human_RBP_ID_1888580,Human_RBP_ID_3581314,Human_RBP_ID_8197785 Human_Splice_Rec_2013699 RMVar_hsa_circ_110054,RMVar_hsa_circ_3786,RMVar_hsa_circ_195075,RMVar_hsa_circ_93168,RMVar_hsa_circ_195074 84625 RMVar_ID_84625 Human_SNP_ID_666290984 m1A Human chr19 - 42230687 42230687 42230687 AAGCTCCTGCCCTGGCTGGGCCCCTAGACTAGAGGGCAGAGGTAAATGAGTCCCTGTCCCCACCT AAGCTCCTGCCCTGGCTGGGCCCCTAGACTAGCGGGCAGAGGTAAATGAGTCCCTGTCCCCACCT T G GSK3A Ensembl:ENSG00000105723 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs924007280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522706,Human_RBP_ID_1888580,Human_RBP_ID_3581314,Human_RBP_ID_8197785 Human_Splice_Rec_2013699 RMVar_hsa_circ_110054,RMVar_hsa_circ_3786,RMVar_hsa_circ_195075,RMVar_hsa_circ_93168,RMVar_hsa_circ_195074 84626 RMVar_ID_84626 Human_SNP_ID_666291004 m1A Human chr19 - 42230779 42230779 42230779 CTCACTAACTCCTCCTGAGGGCCCCACCAAGCACCCTTCCACTTCCATCTGGGAGCCCCAAGAGG CTCACTAACTCCTCCTGAGGGCCCCACCAAGCGCCCTTCCACTTCCATCTGGGAGCCCCAAGAGG T C GSK3A Ensembl:ENSG00000105723 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42230384..42230832 32194978 MeRIP-seq:(Medium) rs1476760986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522711,Human_RBP_ID_1016448,Human_RBP_ID_5116927,Human_RBP_ID_17272696,Human_RBP_ID_17387399,Human_RBP_ID_17568653,Human_RBP_ID_18192296,Human_RBP_ID_26815960 Human_Splice_Rec_2013658,Human_Splice_Rec_2013678,Human_Splice_Rec_2013698,Human_Splice_Rec_2013704 RMVar_hsa_circ_110054,RMVar_hsa_circ_3786,RMVar_hsa_circ_195075,RMVar_hsa_circ_93168,RMVar_hsa_circ_195074 84627 RMVar_ID_84627 Human_SNP_ID_666291475 m1A Human chr19 - 42232477 42232473 42232477 CTTCAGTGCTGGTGGTGAGGGCATAGCCTGGGATCTGGGGAGTGGGGCGGGGTAGGGGGGCAGCC CTTCAGTGCTGGTGGTGAGGGCATAGCCTGGG____GGGGAGTGGGGCGGGGTAGGGGGGCAGCC CAGAT C GSK3A Ensembl:ENSG00000105723 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42232475..42232650 26863196 MeRIP-seq:(Medium) rs1470523787 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_25420261 RMVar_hsa_circ_110054,RMVar_hsa_circ_3786,RMVar_hsa_circ_195075,RMVar_hsa_circ_59626,RMVar_hsa_circ_374115,RMVar_hsa_circ_195076 84628 RMVar_ID_84628 Human_SNP_ID_666293429 m1A Human chr19 - 42240053 42240053 42240053 CCCAAGAAGTGGCTTACACGGACATCAAAGTGATTGGCAATGGCTCATTTGGGGTCGTGTACCAG CCCAAGAAGTGGCTTACACGGACATCAAAGTGGTTGGCAATGGCTCATTTGGGGTCGTGTACCAG T C GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42240051..42240250 26863196 MeRIP-seq:(Medium) rs1472502410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1016458,Human_RBP_ID_1566450,Human_RBP_ID_1888591,Human_RBP_ID_4560234,Human_RBP_ID_8488769,Human_RBP_ID_8834570,Human_RBP_ID_13463648,Human_RBP_ID_18733973 Human_Splice_Rec_2013641,Human_Splice_Rec_2013660,Human_Splice_Rec_2013661,Human_Splice_Rec_2013680,Human_Splice_Rec_2013681,Human_Splice_Rec_2013706,Human_Splice_Rec_2013707 RMVar_hsa_circ_12496,RMVar_hsa_circ_3786,RMVar_hsa_circ_59626,RMVar_hsa_circ_280591,RMVar_hsa_circ_195081,RMVar_hsa_circ_21518 84629 RMVar_ID_84629 Human_SNP_ID_666293440 m1A Human chr19 - 42240093 42240093 42240093 ACCACAGTCGTAGCCACTCTAGGCCAAGGCCCAGAGCGCTCCCAAGAAGTGGCTTACACGGACAT ACCACAGTCGTAGCCACTCTAGGCCAAGGCCCGGAGCGCTCCCAAGAAGTGGCTTACACGGACAT T C GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42240001..42240202 26863196 MeRIP-seq:(Medium) rs1244801063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522733,Human_RBP_ID_3955131,Human_RBP_ID_4560234 Human_Splice_Rec_2013660,Human_Splice_Rec_2013680,Human_Splice_Rec_2013706 RMVar_hsa_circ_12496,RMVar_hsa_circ_3786,RMVar_hsa_circ_59626,RMVar_hsa_circ_280591,RMVar_hsa_circ_195081,RMVar_hsa_circ_21518 84630 RMVar_ID_84630 Human_SNP_ID_666293983 m1A Human chr19 - 42242159 42242159 42242159 AGCTGGGCCGTGAGTACTAGTGGCGCCCGTGTAGGGTGGTGATTAGGGTTCCCAAAGCTCCTCAG AGCTGGGCCGTGAGTACTAGTGGCGCCCGTGTGGGGTGGTGATTAGGGTTCCCAAAGCTCCTCAG T C GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42242154..42242605 26863196 MeRIP-seq:(Medium) rs1275654493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090242 84631 RMVar_ID_84631 Human_SNP_ID_666294169 m1A Human chr19 - 42242576 42242576 42242576 GCGGGCGCTGGGCCGGAGCCGGAGCCCAAGCCAGAGCGGCGCGGCCTGGAAGAGGCCAGGGCCCG GCGGGCGCTGGGCCGGAGCCGGAGCCCAAGCCTGAGCGGCGCGGCCTGGAAGAGGCCAGGGCCCG T A GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:42242475..42242575 26863410 MeRIP-seq:(Medium) rs896733051 Functional Loss SNV dbSNP153 33..33 33 - - - 84632 RMVar_ID_84632 Human_SNP_ID_666294170 m1A Human chr19 - 42242576 42242576 42242576 GCGGGCGCTGGGCCGGAGCCGGAGCCCAAGCCAGAGCGGCGCGGCCTGGAAGAGGCCAGGGCCCG GCGGGCGCTGGGCCGGAGCCGGAGCCCAAGCCGGAGCGGCGCGGCCTGGAAGAGGCCAGGGCCCG T C GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:42242475..42242575 26863410 MeRIP-seq:(Medium) rs896733051 Functional Loss SNV dbSNP153 33..33 33 - - - 84633 RMVar_ID_84633 Human_SNP_ID_666296135 m1A Human chr19 - 42248778 42248778 42248778 GTCGGAGGAGGTAGAGGTGACTGACATCAGTGATGAGGATGAGGAAGACGGGGAGGTGTTCAAGA GTCGGAGGAGGTAGAGGTGACTGACATCAGTGGTGAGGATGAGGAAGACGGGGAGGTGTTCAAGA T C ERF,AC006486.1 Ensembl:ENSG00000105722,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42248776..42248875 26863196 MeRIP-seq:(Medium) rs768716522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6766966,Human_RBP_ID_13463680,Human_RBP_ID_23799401,Human_RBP_ID_27468676 Human_miRNA_ID_208481 84634 RMVar_ID_84634 Human_SNP_ID_666296290 m1A Human chr19 + 42249063 42249063 42249063 GGACCGGTGGGGTCTCGGGTGCCATGGGCGGCAGCGGGCACTTGTCAGGGCGCTGGGGCTGGGGC GGACCGGTGGGGTCTCGGGTGCCATGGGCGGCCGCGGGCACTTGTCAGGGCGCTGGGGCTGGGGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:42240076..42255083 26863410 MeRIP-seq:(Medium) rs1421470935 Functional Loss SNV dbSNP153 33..33 33 - - - 84635 RMVar_ID_84635 Human_SNP_ID_666296510 m1A Human chr19 - 42249557 42249557 42249557 GCTGTGGTGGCCCGCCGCCTGGGCCGAGGCTCAGTCAGTGACTGTAGTGATGGCACGTCAGAGCT GCTGTGGTGGCCCGCCGCCTGGGCCGAGGCTCTGTCAGTGACTGTAGTGATGGCACGTCAGAGCT T A ERF,AC006486.1 Ensembl:ENSG00000105722,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42249551..42249625 26863196 MeRIP-seq:(Medium) rs372627614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241435,Human_RBP_ID_27275027 84636 RMVar_ID_84636 Human_SNP_ID_666298167 m1A Human chr19 + 42254115 42254108 42254115 GGGGAGTTAATCCCGCTGCCCCCCGCCCGCCGACCGAGGGGGAGGGGAACCTTGGCCCCTTAAGG GGGGAGTTAATCCCGCTGCCCCCCGC_______CCGAGGGGGAGGGGAACCTTGGCCCCTTAAGG CCCGCCGA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42254101..42254316 26863196 MeRIP-seq:(Medium) rs1338173204 Functional Loss DEL dbSNP153 27..33 33 - - - 84637 RMVar_ID_84637 Human_SNP_ID_666303387 m1A Human chr19 + 42271905 42271903 42271906 GCGGCGAGGGGCTGGGGAGGGTGACAAGCCAGAGGAGGAGGATGACGAGGCACAGCAGCCGCAAC GCGGCGAGGGGCTGGGGAGGGTGACAAGCCA___GAGGAGGATGACGAGGCACAGCAGCCGCAAC AGAG A CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42269291..42272265 26863196 MeRIP-seq:(Medium) rs1398849295 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5527023 RMVar_hsa_circ_33021 84638 RMVar_ID_84638 Human_SNP_ID_666306332 m1A Human chr19 + 42284070 42284070 42284070 GGAGGGGAGCGCGTAGTAGTGGCGGGGCGGGGAGGCGGTGGTGGTTCGGCGCGGGGCTCGCTCGG GGAGGGGAGCGCGTAGTAGTGGCGGGGCGGGGGGGCGGTGGTGGTTCGGCGCGGGGCTCGCTCGG A G CIC Ensembl:ENSG00000079432 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42284065..42286900 26863196 MeRIP-seq:(Medium) rs187522860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8416,Human_RBP_ID_241129,Human_RBP_ID_263287,Human_RBP_ID_824364,Human_RBP_ID_3581343,Human_RBP_ID_4532479,Human_RBP_ID_5191909,Human_RBP_ID_5320423,Human_RBP_ID_8103079,Human_RBP_ID_8196583,Human_RBP_ID_8728083,Human_RBP_ID_8942461,Human_RBP_ID_9328989,Human_RBP_ID_9425358,Human_RBP_ID_18420940,Human_RBP_ID_18461316,Human_RBP_ID_18492845,Human_RBP_ID_21978014,Human_RBP_ID_22371177,Human_RBP_ID_22718371,Human_RBP_ID_26783787 84639 RMVar_ID_84639 Human_SNP_ID_666306337 m1A Human chr19 - 42284079 42284079 42284079 CCGTGCGCTCCGAGCGAGCCCCGCGCCGAACCACCACCGCCTCCCCGCCCCGCCACTACTACGCG CCGTGCGCTCCGAGCGAGCCCCGCGCCGAACCGCCACCGCCTCCCCGCCCCGCCACTACTACGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42284076..42284379 26863196 MeRIP-seq:(Medium) rs184104469 Functional Loss SNV dbSNP153 33..33 33 - - - 84640 RMVar_ID_84640 Human_SNP_ID_666306338 m1A Human chr19 - 42284079 42284079 42284079 CCGTGCGCTCCGAGCGAGCCCCGCGCCGAACCACCACCGCCTCCCCGCCCCGCCACTACTACGCG CCGTGCGCTCCGAGCGAGCCCCGCGCCGAACCCCCACCGCCTCCCCGCCCCGCCACTACTACGCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42284076..42284379 26863196 MeRIP-seq:(Medium) rs184104469 Functional Loss SNV dbSNP153 33..33 33 - - - 84641 RMVar_ID_84641 Human_SNP_ID_666306386 m1A Human chr19 + 42284211 42284202 42284211 GGGGCCCGGAAAGGCGGGGCGGCGGCGCCGGCAGCCGGGACGCGCGGGGCCAGAGCCGTTACCCG GGGGCCCGGAAAGGCGGGGCGGCG_________GCCGGGACGCGCGGGGCCAGAGCCGTTACCCG GGCGCCGGCA G CIC Ensembl:ENSG00000079432 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:42284110..42284337 26863410 MeRIP-seq:(Medium) rs972766638 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_3583754,Human_RBP_ID_8196584,Human_RBP_ID_21978015,Human_RBP_ID_24375968 84642 RMVar_ID_84642 Human_SNP_ID_666306394 m1A Human chr19 + 42284218 42284218 42284218 GGAAAGGCGGGGCGGCGGCGCCGGCAGCCGGGACGCGCGGGGCCAGAGCCGTTACCCGCCGGAGC GGAAAGGCGGGGCGGCGGCGCCGGCAGCCGGGTCGCGCGGGGCCAGAGCCGTTACCCGCCGGAGC A T CIC Ensembl:ENSG00000079432 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:42284051..42284472;chr19:42284051..42287019 26863196 MeRIP-seq:(Medium) rs946890060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4532486,Human_RBP_ID_8196584,Human_RBP_ID_21978015 84643 RMVar_ID_84643 Human_SNP_ID_666307088 m1A Human chr19 + 42286074 42286074 42286074 GGACTACAGATAAGCCGAGGGGCTGATGGGGAAGGGAGGCTGGGAGGCCGATTTCTGGATGGTGC GGACTACAGATAAGCCGAGGGGCTGATGGGGAGGGGAGGCTGGGAGGCCGATTTCTGGATGGTGC A G CIC Ensembl:ENSG00000079432 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42286068..42286365 26863196 MeRIP-seq:(Medium) rs1213718050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5321708,Human_RBP_ID_17190837,Human_RBP_ID_18492846,Human_RBP_ID_18733996 RMVar_hsa_circ_195084,RMVar_hsa_circ_80743 84644 RMVar_ID_84644 Human_SNP_ID_666308719 m1A Human chr19 + 42290313 42290313 42290313 CACTGCCGCCCCCCACTGGACCCTGAGCCCCCAGGGCCCCCGGATCCTCCTGTAGCCTTTGGCAA CACTGCCGCCCCCCACTGGACCCTGAGCCCCCCGGGCCCCCGGATCCTCCTGTAGCCTTTGGCAA A C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42290306..42290405 26863196 MeRIP-seq:(Medium) rs1265184268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239247,Human_RBP_ID_522768 Human_Splice_Rec_2013762,Human_Splice_Rec_2013802,Human_Splice_Rec_2013840 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_96147,RMVar_hsa_circ_78643,RMVar_hsa_circ_114435,RMVar_hsa_circ_195088,RMVar_hsa_circ_195089,RMVar_hsa_circ_119989,RMVar_hsa_circ_195090,RMVar_hsa_circ_195091 84645 RMVar_ID_84645 Human_SNP_ID_666308746 m1A Human chr19 - 42290352 42290352 42290352 GGCGAGGACGCAGAGGAGGATGGGGCGGAACCATAGCCTTTGCCAAAGGCTACAGGAGGATCCGG GGCGAGGACGCAGAGGAGGATGGGGCGGAACCGTAGCCTTTGCCAAAGGCTACAGGAGGATCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42290344..42290532 26863196 MeRIP-seq:(Medium) rs1487314557 Functional Loss SNV dbSNP153 33..33 33 - - - 84646 RMVar_ID_84646 Human_SNP_ID_666308766 m1A Human chr19 - 42290385 42290385 42290385 AAGGAGGTGGCTGCCGAGGCTGAGGAGGAAGCAGGCGAGGACGCAGAGGAGGATGGGGCGGAACC AAGGAGGTGGCTGCCGAGGCTGAGGAGGAAGCCGGCGAGGACGCAGAGGAGGATGGGGCGGAACC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42290376..42290425 26863196 MeRIP-seq:(Medium) rs750645309 Functional Loss SNV dbSNP153 33..33 33 - - - 84647 RMVar_ID_84647 Human_SNP_ID_666309056 m1A Human chr19 - 42290929 42290929 42290929 GTCCGAATACACTAAGCTGACACCCAGCGGGGAGCCCCCAGGCACCCGAGACCCAGTGCCCATTT GTCCGAATACACTAAGCTGACACCCAGCGGGGGGCCCCCAGGCACCCGAGACCCAGTGCCCATTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42289866..42291397 32194978 MeRIP-seq:(Medium) rs765947900 Functional Loss SNV dbSNP153 33..33 33 - - - 84648 RMVar_ID_84648 Human_SNP_ID_666309057 m1A Human chr19 - 42290929 42290929 42290929 GTCCGAATACACTAAGCTGACACCCAGCGGGGAGCCCCCAGGCACCCGAGACCCAGTGCCCATTT GTCCGAATACACTAAGCTGACACCCAGCGGGGCGCCCCCAGGCACCCGAGACCCAGTGCCCATTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42289866..42291397 32194978 MeRIP-seq:(Medium) rs765947900 Functional Loss SNV dbSNP153 33..33 33 - - - 84649 RMVar_ID_84649 Human_SNP_ID_666309236 m1A Human chr19 - 42291336 42291336 42291336 GGGAGGGTGAAACGGATGCTGGTGGTGGGTGCAGGGCCGCTGGGAGCCGCTGCCTTGGTCCCAGG GGGAGGGTGAAACGGATGCTGGTGGTGGGTGCGGGGCCGCTGGGAGCCGCTGCCTTGGTCCCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:42291325..42291455;chr19:42291287..42291421 26863196 MeRIP-seq:(Medium) rs1202908082 Functional Loss SNV dbSNP153 33..33 33 - - - 84650 RMVar_ID_84650 Human_SNP_ID_666309472 m1A Human chr19 - 42291717 42291717 42291717 TCACCTTGCTGGGGGGCTGGGCACCATTCTGCACAGGTACTGAGAAGGGCGGGCTCACCAGTGGC TCACCTTGCTGGGGGGCTGGGCACCATTCTGCTCAGGTACTGAGAAGGGCGGGCTCACCAGTGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42291587..42292128 32194978 MeRIP-seq:(Medium) rs775981157 Functional Loss SNV dbSNP153 33..33 33 - - - 84651 RMVar_ID_84651 Human_SNP_ID_666309674 m1A Human chr19 + 42292154 42292154 42292154 AGCGGCCTGGTGCCGCCCCTGAGCCCAGCCACACTCCCTGGACCCACCTCTCAGCCTCAGAAGGT AGCGGCCTGGTGCCGCCCCTGAGCCCAGCCACGCTCCCTGGACCCACCTCTCAGCCTCAGAAGGT A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42292151..42292478 26863196 MeRIP-seq:(Medium) rs1278011643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957045 Human_Splice_Rec_2013766,Human_Splice_Rec_2013767,Human_Splice_Rec_2013806,Human_Splice_Rec_2013807,Human_Splice_Rec_2013844,Human_Splice_Rec_2013845 Human_miRNA_ID_1961040,Human_miRNA_ID_2910774 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_96147,RMVar_hsa_circ_78643,RMVar_hsa_circ_114435,RMVar_hsa_circ_195088,RMVar_hsa_circ_195089,RMVar_hsa_circ_119989,RMVar_hsa_circ_195090,RMVar_hsa_circ_195091,RMVar_hsa_circ_84540,RMVar_hsa_circ_195092 84652 RMVar_ID_84652 Human_SNP_ID_666309773 m1A Human chr19 + 42292329 42292329 42292329 CAGAATCACCTATGTGCAGTCAGCGGGCGGGCACGCGCTGCCCCTGGGTACCAGCCCTGCGTCCA CAGAATCACCTATGTGCAGTCAGCGGGCGGGCGCGCGCTGCCCCTGGGTACCAGCCCTGCGTCCA A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42292326..42292819 26863196 MeRIP-seq:(Medium) rs1199168755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3955148,Human_RBP_ID_5373976,Human_RBP_ID_17272157,Human_RBP_ID_18997973,Human_RBP_ID_23210976,Human_RBP_ID_23257537 Human_Splice_Rec_2013768,Human_Splice_Rec_2013808,Human_Splice_Rec_2013846 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_96147,RMVar_hsa_circ_114435,RMVar_hsa_circ_195088,RMVar_hsa_circ_195089,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091,RMVar_hsa_circ_84540,RMVar_hsa_circ_195092 84653 RMVar_ID_84653 Human_SNP_ID_666309822 m1A Human chr19 + 42292418 42292418 42292418 ACGGGCCCACGAGCTCTGTAGCTCTAGGCTTCACCTCGCTGGGGCCCAGCGGCCCCGCCTTCGTG ACGGGCCCACGAGCTCTGTAGCTCTAGGCTTCGCCTCGCTGGGGCCCAGCGGCCCCGCCTTCGTG A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42292369..42292619 32194978 MeRIP-seq:(Medium) rs778905836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26815970 Human_Splice_Rec_2013769,Human_Splice_Rec_2013809,Human_Splice_Rec_2013847 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_96147,RMVar_hsa_circ_114435,RMVar_hsa_circ_195088,RMVar_hsa_circ_195089,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091,RMVar_hsa_circ_84540,RMVar_hsa_circ_195092 84654 RMVar_ID_84654 Human_SNP_ID_666309918 m1A Human chr19 + 42292609 42292609 42292609 CCACTGCTGGCTCCCGGTCAGGTGGGCGTGTCACCTGTGCCCAGTCCCCAGCTGCCGCCTGCCTG CCACTGCTGGCTCCCGGTCAGGTGGGCGTGTCCCCTGTGCCCAGTCCCCAGCTGCCGCCTGCCTG A C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:42292601..42292625;chr19:42292601..42292850 26863196 MeRIP-seq:(Medium) rs970136849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25440808 Human_Splice_Rec_2013770,Human_Splice_Rec_2013810,Human_Splice_Rec_2013848 Human_miRNA_ID_2686266,Human_miRNA_ID_2891253 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_114435,RMVar_hsa_circ_195089,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84655 RMVar_ID_84655 Human_SNP_ID_666310182 m1A Human chr19 + 42293135 42293135 42293135 AGCCTCTGGAGCCTGGCCCAGTCCGAGAGCCAACTGCCCCAGAGTCTGAGCTTGAGGGGCAGCCC AGCCTCTGGAGCCTGGCCCAGTCCGAGAGCCACCTGCCCCAGAGTCTGAGCTTGAGGGGCAGCCC A C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42293014..42293214 32194978 MeRIP-seq:(Medium) rs1480783036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957048,Human_RBP_ID_18734015 Human_miRNA_ID_936024,Human_miRNA_ID_2425664,Human_miRNA_ID_2435332,Human_miRNA_ID_2784743 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84656 RMVar_ID_84656 Human_SNP_ID_666310183 m1A Human chr19 + 42293135 42293135 42293135 AGCCTCTGGAGCCTGGCCCAGTCCGAGAGCCAACTGCCCCAGAGTCTGAGCTTGAGGGGCAGCCC AGCCTCTGGAGCCTGGCCCAGTCCGAGAGCCAGCTGCCCCAGAGTCTGAGCTTGAGGGGCAGCCC A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42293014..42293214 32194978 MeRIP-seq:(Medium) rs1480783036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957048,Human_RBP_ID_18734015 Human_miRNA_ID_936024,Human_miRNA_ID_2425664,Human_miRNA_ID_2435332,Human_miRNA_ID_2784743 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84657 RMVar_ID_84657 Human_SNP_ID_666310447 m1A Human chr19 + 42293712 42293709 42293712 CGGCCCCAGCTCCAGCTGTAGCCCCTGGTGGCAGCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG CGGCCCCAGCTCCAGCTGTAGCCCCTGGTG___GCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG GGCA G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42293703..42293768 26863196 MeRIP-seq:(Medium) rs753719289 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84658 RMVar_ID_84658 Human_SNP_ID_666310451 m1A Human chr19 + 42293712 42293712 42293712 CGGCCCCAGCTCCAGCTGTAGCCCCTGGTGGCAGCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG CGGCCCCAGCTCCAGCTGTAGCCCCTGGTGGCGGCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42293703..42293768 26863196 MeRIP-seq:(Medium) rs779189227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84659 RMVar_ID_84659 Human_SNP_ID_666310452 m1A Human chr19 + 42293712 42293712 42293712 CGGCCCCAGCTCCAGCTGTAGCCCCTGGTGGCAGCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG CGGCCCCAGCTCCAGCTGTAGCCCCTGGTGGCTGCAGCGAGAGCAGCAGTGGGCGGGCAGCCGGG A T CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42293703..42293768 26863196 MeRIP-seq:(Medium) rs779189227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84660 RMVar_ID_84660 Human_SNP_ID_666310582 m1A Human chr19 + 42293962 42293962 42293962 TCCAGCAGGGTCCTGTCAGAAGTGGACTTCGAAGAGCGCTTTGCTGAGTTGCCTGAGTTTCGGCC TCCAGCAGGGTCCTGTCAGAAGTGGACTTCGAGGAGCGCTTTGCTGAGTTGCCTGAGTTTCGGCC A G CIC Ensembl:ENSG00000079432 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42293673..42294022 32194978 MeRIP-seq:(Medium) rs1450332075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1566466,Human_RBP_ID_1888602,Human_RBP_ID_3572614,Human_RBP_ID_8488800,Human_RBP_ID_8834620,Human_RBP_ID_26336359 Human_Splice_Rec_2013776,Human_Splice_Rec_2013816,Human_Splice_Rec_2013854,Human_Splice_Rec_2013862,Human_Splice_Rec_2013870,Human_Splice_Rec_2013878 Human_miRNA_ID_2795882,Human_miRNA_ID_2796298,Human_miRNA_ID_2796712,Human_miRNA_ID_2797129,Human_miRNA_ID_2799476,Human_miRNA_ID_2883498 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_79125,RMVar_hsa_circ_195087,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84661 RMVar_ID_84661 Human_SNP_ID_666310912 m1A Human chr19 + 42294913 42294910 42294913 GTCTGCAGTTGAAGATCCGTGAGGTGCGCCAGAAGATCATGCAGGCTGCCACTCCCACGGAGCAG GTCTGCAGTTGAAGATCCGTGAGGTGCGCC___AGATCATGCAGGCTGCCACTCCCACGGAGCAG CAGA C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42294904..42295124 26863196 MeRIP-seq:(Medium) rs751580245 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_522775 Human_Splice_Rec_2013782,Human_Splice_Rec_2013822,Human_Splice_Rec_2013860,Human_Splice_Rec_2013868,Human_Splice_Rec_2013876,Human_Splice_Rec_2013884,Human_Splice_Rec_2013886 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84662 RMVar_ID_84662 Human_SNP_ID_666310927 m1A Human chr19 + 42294954 42294954 42294954 CAGGCTGCCACTCCCACGGAGCAGCCCCCTGGAGCTGAGGCTCCTCTCCCTGTACCGCCCCCCAC CAGGCTGCCACTCCCACGGAGCAGCCCCCTGGCGCTGAGGCTCCTCTCCCTGTACCGCCCCCCAC A C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42294903..42295037 26863196 MeRIP-seq:(Medium) rs1447804915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522777,Human_RBP_ID_18945582 Human_miRNA_ID_2209535,Human_miRNA_ID_3034141 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 84663 RMVar_ID_84663 Human_SNP_ID_666311686 m1A Human chr19 - 42297121 42297121 42297121 TCTGCACTCCCTGCTTCTGCGTCTGCTGGCCCAAGACCAGGGCCAAGGTGCTCCCCTGCTGGAGC TCTGCACTCCCTGCTTCTGCGTCTGCTGGCCCGAGACCAGGGCCAAGGTGCTCCCCTGCTGGAGC T C PAFAH1B3 Ensembl:ENSG00000079462 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42297051..42297325 32194978 MeRIP-seq:(Medium) rs763739992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522784,Human_RBP_ID_5116289,Human_RBP_ID_17656174,Human_RBP_ID_18166067,Human_RBP_ID_18192304,Human_RBP_ID_22448771,Human_RBP_ID_22762998 Human_miRNA_ID_594212,Human_miRNA_ID_1265201,Human_miRNA_ID_1336808,Human_miRNA_ID_1353716,Human_miRNA_ID_2218798,Human_miRNA_ID_2427766,Human_miRNA_ID_2663658,Human_miRNA_ID_2682113 RMVar_hsa_circ_195093,RMVar_hsa_circ_115880,RMVar_hsa_circ_119464,RMVar_hsa_circ_195094 84664 RMVar_ID_84664 Human_SNP_ID_666312638 m1A Human chr19 + 42300272 42300272 42300272 AATGCCAAAGTTAAGTGCATGCAGAGGAGAGAAGAGCTCGCGCCAGATCTGTGGGCAAGAAGTGG AATGCCAAAGTTAAGTGCATGCAGAGGAGAGACGAGCTCGCGCCAGATCTGTGGGCAAGAAGTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42300251..42302625 26863196 MeRIP-seq:(Medium) rs1234681660 Functional Loss SNV dbSNP153 33..33 33 - - - 84665 RMVar_ID_84665 Human_SNP_ID_666313006 m1A Human chr19 + 42301855 42301852 42301855 AGAGCCTCGGGCTGCCTGAGGCCAATCTGGGTACTCTCATAATACCTCACCTGGCCTGGGTTCTG AGAGCCTCGGGCTGCCTGAGGCCAATCTGG___CTCTCATAATACCTCACCTGGCCTGGGTTCTG GGTA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:42301852..42302584 26863196 MeRIP-seq:(Medium) rs1460990518 Functional Loss DEL dbSNP153 31..33 33 - - - 84666 RMVar_ID_84666 Human_SNP_ID_666313174 m1A Human chr19 - 42302299 42302299 42302299 CTGCAGGAGCTGCGGCGCCAAGATGAGTGGAGAGGAGAACCCAGCCAGCAAGCCCACGCCGGTGC CTGCAGGAGCTGCGGCGCCAAGATGAGTGGAGTGGAGAACCCAGCCAGCAAGCCCACGCCGGTGC T A PAFAH1B3 Ensembl:ENSG00000079462 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42300001..42306992 26863196 MeRIP-seq:(Medium) rs1203158458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4559656,Human_RBP_ID_5145784 Human_Splice_Rec_2013887,Human_Splice_Rec_2013896,Human_Splice_Rec_2013897,Human_Splice_Rec_2013905,Human_Splice_Rec_2013914,Human_Splice_Rec_2013915,Human_Splice_Rec_2013924,Human_Splice_Rec_2013925,Human_Splice_Rec_2013933,Human_Splice_Rec_2013938,Human_Splice_Rec_2013939,Human_Splice_Rec_2013946,Human_Splice_Rec_2013947 Human_miRNA_ID_2333381,Human_miRNA_ID_2966465 RMVar_hsa_circ_195093,RMVar_hsa_circ_119464,RMVar_hsa_circ_32344,RMVar_hsa_circ_39126 84667 RMVar_ID_84667 Human_SNP_ID_666316295 m1A Human chr19 + 42313344 42313344 42313344 CGCTCTCGCCTCCATTGCCGGGCCAGTGCGGGAGCCGGAGCGGAGCCGGGGCCGGAGCGGGCGGA CGCTCTCGCCTCCATTGCCGGGCCAGTGCGGGGGCCGGAGCGGAGCCGGGGCCGGAGCGGGCGGA A G TMEM145 Ensembl:ENSG00000167619 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42313341..42313442 26863196 MeRIP-seq:(Medium) rs901485189 Functional Loss SNV dbSNP153 33..33 33 - - - 84668 RMVar_ID_84668 Human_SNP_ID_666319901 m1A Human chr19 - 42325678 42325676 42325678 GGACCCCACAGACCCAATCCCTTTGCTCACCCACCCTCGCCTCCCTCCGAAGCCGGATGGGCCAG GGACCCCACAGACCCAATCCCTTTGCTCACCC__CCTCGCCTCCCTCCGAAGCCGGATGGGCCAG GGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr19:42325673..42325799;chr19:42325671..42325869 26863196 MeRIP-seq:(Medium) rs1288540111 Functional Loss DEL dbSNP153 33..34 33 - - - 84669 RMVar_ID_84669 Human_SNP_ID_666319906 m1A Human chr19 + 42325693 42325693 42325693 TCGGAGGGAGGCGAGGGTGGGTGAGCAAAGGGATTGGGTCTGTGGGGTCCAGGCCCGAACCCCTG TCGGAGGGAGGCGAGGGTGGGTGAGCAAAGGGGTTGGGTCTGTGGGGTCCAGGCCCGAACCCCTG A G MEGF8 Ensembl:ENSG00000105429 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42325688..42325859 26863196 MeRIP-seq:(Medium) rs987519039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_770858,Human_RBP_ID_825581,Human_RBP_ID_4532728,Human_RBP_ID_18421415,Human_RBP_ID_26990879 Human_miRNA_ID_2142642,Human_miRNA_ID_2193767,Human_miRNA_ID_2207976,Human_miRNA_ID_2509901,Human_miRNA_ID_3046451 RMVar_hsa_circ_123052,RMVar_hsa_circ_195101 84670 RMVar_ID_84670 Human_SNP_ID_666319909 m1A Human chr19 + 42325719 42325698 42325720 AAAGGGATTGGGTCTGTGGGGTCCAGGCCCGAACCCCTGAAGACGGGCTCCGCCCCCGGCACCCG AAAGGGATTGGG______________________CCCTGAAGACGGGCTCCGCCCCCGGCACCCG GTCTGTGGGGTCCAGGCCCGAAC G MEGF8 Ensembl:ENSG00000105429 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42325711..42325859 26863196 MeRIP-seq:(Medium) rs1430011637 Functional Loss DEL dbSNP153 13..34 33 - - - Human_RBP_ID_825581,Human_RBP_ID_913574,Human_RBP_ID_4557536,Human_RBP_ID_18421415 RMVar_hsa_circ_123052,RMVar_hsa_circ_195101 84671 RMVar_ID_84671 Human_SNP_ID_666324513 m1A Human chr19 + 42343670 42343670 42343670 ACTGGGGTGACAGGGAAAGGGTGGCTGGGGGGAGGAGGTAGCAGGGTTTCCACAGGTGAGGGGAA ACTGGGGTGACAGGGAAAGGGTGGCTGGGGGGGGGAGGTAGCAGGGTTTCCACAGGTGAGGGGAA A G MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42343661..42343792 26863196 MeRIP-seq:(Medium) rs1049991746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825586,Human_RBP_ID_21978027 RMVar_hsa_circ_85175,RMVar_hsa_circ_123052,RMVar_hsa_circ_102022,RMVar_hsa_circ_195101,RMVar_hsa_circ_195103,RMVar_hsa_circ_117248,RMVar_hsa_circ_195104,RMVar_hsa_circ_304768,RMVar_hsa_circ_128071,RMVar_hsa_circ_195107,RMVar_hsa_circ_195108,RMVar_hsa_circ_95674,RMVar_hsa_circ_195109,RMVar_hsa_circ_332188,RMVar_hsa_circ_272419,RMVar_hsa_circ_335618,RMVar_hsa_circ_195110,RMVar_hsa_circ_195111 84672 RMVar_ID_84672 Human_SNP_ID_666330704 m1A Human chr19 - 42363421 42363421 42363421 ACAGGGACCCTCATGAGGCAACGAGGGAGGAAAGAGATGGTGGCACGAGAAGGAAGCACGACTGC ACAGGGACCCTCATGAGGCAACGAGGGAGGAAGGAGATGGTGGCACGAGAAGGAAGCACGACTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42363411..42363512 26863196 MeRIP-seq:(Medium) rs1172037239 Functional Loss SNV dbSNP153 33..33 33 - - - 84673 RMVar_ID_84673 Human_SNP_ID_666332785 m1A Human chr19 + 42370882 42370882 42370882 GGGGGGGGGGGGGGGGGGGGGGGAGGCCGGGGATCCCACCCTTCTCACTGGGAGTAGCTCTGGAG GGGGGGGGGGGGGGGGGGGGGGGAGGCCGGGGGTCCCACCCTTCTCACTGGGAGTAGCTCTGGAG A G MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:42370814..42370888;chr19:42370749..42370900 26863196 MeRIP-seq:(Medium) rs563391903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86381,RMVar_hsa_circ_122934,RMVar_hsa_circ_195115,RMVar_hsa_circ_195114,RMVar_hsa_circ_85774,RMVar_hsa_circ_195126,RMVar_hsa_circ_344687,RMVar_hsa_circ_25054,RMVar_hsa_circ_195134 84674 RMVar_ID_84674 Human_SNP_ID_666332786 m1A Human chr19 + 42370882 42370882 42370882 GGGGGGGGGGGGGGGGGGGGGGGAGGCCGGGGATCCCACCCTTCTCACTGGGAGTAGCTCTGGAG GGGGGGGGGGGGGGGGGGGGGGGAGGCCGGGGTTCCCACCCTTCTCACTGGGAGTAGCTCTGGAG A T MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:42370814..42370888;chr19:42370749..42370900 26863196 MeRIP-seq:(Medium) rs563391903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86381,RMVar_hsa_circ_122934,RMVar_hsa_circ_195115,RMVar_hsa_circ_195114,RMVar_hsa_circ_85774,RMVar_hsa_circ_195126,RMVar_hsa_circ_344687,RMVar_hsa_circ_25054,RMVar_hsa_circ_195134 84675 RMVar_ID_84675 Human_SNP_ID_666332787 m1A Human chr19 - 42370883 42370883 42370883 GCTCCAGAGCTACTCCCAGTGAGAAGGGTGGGATCCCCGGCCTCCCCCCCCCCCCCCCCCCCCCC GCTCCAGAGCTACTCCCAGTGAGAAGGGTGGGGTCCCCGGCCTCCCCCCCCCCCCCCCCCCCCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:42370747..42370900;chr19:42370826..42370900 26863196 MeRIP-seq:(Medium) rs1214416279 Functional Loss SNV dbSNP153 33..33 33 - - - 84676 RMVar_ID_84676 Human_SNP_ID_666333833 m1A Human chr19 + 42374822 42374822 42374822 CGCTAAGGAAAGTTAAGTAGGAAGCGGGGGCTAGGGCTGTTGGGGAGTGGGAATGGTAGACGCAG CGCTAAGGAAAGTTAAGTAGGAAGCGGGGGCTGGGGCTGTTGGGGAGTGGGAATGGTAGACGCAG A G MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42374788..42374933 26863196 MeRIP-seq:(Medium) rs1022902471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_824722 RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 84677 RMVar_ID_84677 Human_SNP_ID_666334667 m1A Human chr19 + 42377327 42377323 42377327 CTTGTTTTATTGGAAGGACCAGAAAACTGGTAAGTGTGACCCAGATCAAGTGTGAGGAGATGAGG CTTGTTTTATTGGAAGGACCAGAAAACTG____GTGTGACCCAGATCAAGTGTGAGGAGATGAGG GGTAA G MEGF8 Ensembl:ENSG00000105429 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:42377172..42377622;chr19:42377280..42377372 26863196 MeRIP-seq:(Medium) rs1375782056 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_9353600,Human_RBP_ID_13463957,Human_RBP_ID_17935936,Human_RBP_ID_20397487 RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 84678 RMVar_ID_84678 Human_SNP_ID_666334694 m1A Human chr19 - 42377447 42377438 42377448 GATCCTGTCACTCCCCTTCATCAAACCATCCAACAGCTTCCCATTGCCCTGAGAATAAAACCCAA GATCCTGTCACTCCCCTTCATCAAACCATCC__________CATTGCCCTGAGAATAAAACCCAA GGGAAGCTGTT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:42377329..42377577 26863196 MeRIP-seq:(Medium) rs1462197130 Functional Loss DEL dbSNP153 32..41 33 - - - 84679 RMVar_ID_84679 Human_SNP_ID_666334696 m1A Human chr19 - 42377447 42377447 42377447 GATCCTGTCACTCCCCTTCATCAAACCATCCAACAGCTTCCCATTGCCCTGAGAATAAAACCCAA GATCCTGTCACTCCCCTTCATCAAACCATCCAGCAGCTTCCCATTGCCCTGAGAATAAAACCCAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:42377329..42377577 26863196 MeRIP-seq:(Medium) rs1165653101 Functional Loss SNV dbSNP153 33..33 33 - - - 84680 RMVar_ID_84680 Human_SNP_ID_666334818 m1A Human chr19 + 42377891 42377891 42377891 GCAGGGATGGTGGGCTGGAGTAGGGTGCTGGCAATGAGGGAGTCTGGCTCAGATGTGGGATGTGT GCAGGGATGGTGGGCTGGAGTAGGGTGCTGGCCATGAGGGAGTCTGGCTCAGATGTGGGATGTGT A C MEGF8 Ensembl:ENSG00000105429 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42377721..42378134 26863196 MeRIP-seq:(Medium) rs1303277784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4569664,Human_RBP_ID_5443176,Human_RBP_ID_6767091,Human_RBP_ID_8198867,Human_RBP_ID_9353743,Human_RBP_ID_18305535,Human_RBP_ID_22979447,Human_RBP_ID_23799473 Human_miRNA_ID_2404575 RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 84681 RMVar_ID_84681 Human_SNP_ID_666334819 m1A Human chr19 + 42377891 42377891 42377891 GCAGGGATGGTGGGCTGGAGTAGGGTGCTGGCAATGAGGGAGTCTGGCTCAGATGTGGGATGTGT GCAGGGATGGTGGGCTGGAGTAGGGTGCTGGCGATGAGGGAGTCTGGCTCAGATGTGGGATGTGT A G MEGF8 Ensembl:ENSG00000105429 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42377721..42378134 26863196 MeRIP-seq:(Medium) rs1303277784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4569664,Human_RBP_ID_5443176,Human_RBP_ID_6767091,Human_RBP_ID_8198867,Human_RBP_ID_9353743,Human_RBP_ID_18305535,Human_RBP_ID_22979447,Human_RBP_ID_23799473 Human_miRNA_ID_2404575 RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 84682 RMVar_ID_84682 Human_SNP_ID_666334828 m1A Human chr19 + 42377932 42377932 42377932 GTCTGGCTCAGATGTGGGATGTGTATGGAAGAATATAAATGATGGTGTGGATGTCAGGGTGAGGG GTCTGGCTCAGATGTGGGATGTGTATGGAAGAGTATAAATGATGGTGTGGATGTCAGGGTGAGGG A G MEGF8 Ensembl:ENSG00000105429 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42377771..42378061 26863196 MeRIP-seq:(Medium) rs191355802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1888621,Human_RBP_ID_2566525,Human_RBP_ID_9353743,Human_RBP_ID_18305536,Human_RBP_ID_22973612,Human_RBP_ID_23799473,Human_RBP_ID_26468627 RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 84683 RMVar_ID_84683 Human_SNP_ID_666337273 m1A Human chr19 + 42387408 42387408 42387408 GGAGTGCAGGCCTCCGGGCAGGTAGGGCGCGCAGCAGCACTCGCCAAAGTCGTCGGAGATGCGGC GGAGTGCAGGCCTCCGGGCAGGTAGGGCGCGCTGCAGCACTCGCCAAAGTCGTCGGAGATGCGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:42387062..42387440;chr19:42387122..42387421 26863196 MeRIP-seq:(Medium) rs758089800 Functional Loss SNV dbSNP153 33..33 33 - - - 84684 RMVar_ID_84684 Human_SNP_ID_666337709 m1A Human chr19 - 42388711 42388711 42388711 GATACTACCTCATGCCTTCCCACACTCAACTTATCAGGCCCTCAACCTCCCCTTTGCATGCTCAG GATACTACCTCATGCCTTCCCACACTCAACTTCTCAGGCCCTCAACCTCCCCTTTGCATGCTCAG T G CNFN Ensembl:ENSG00000105427 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42388662..42388772 26863196 MeRIP-seq:(Medium) rs12165114 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10112,GWAS_ID_10113,GWAS_ID_10114 84685 RMVar_ID_84685 Human_SNP_ID_666337715 m1A Human chr19 + 42388750 42388750 42388750 AGTGTGGGAAGGCATGAGGTAGTATCCTAAGGAGTGTTGGGGGTCTGAGGAAAGGGTGACTGTTA AGTGTGGGAAGGCATGAGGTAGTATCCTAAGGGGTGTTGGGGGTCTGAGGAAAGGGTGACTGTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42388645..42388832 26863196 MeRIP-seq:(Medium) rs549162284 Functional Loss SNV dbSNP153 33..33 33 - - - 84686 RMVar_ID_84686 Human_SNP_ID_666339813 m1A Human chr19 - 42397216 42397216 42397216 CTAGGCGTGCTGGAAAGGGCTTACCCGGCCAGACTCGGAGAACCCGTTCCCTCGCGAGCCCGCTC CTAGGCGTGCTGGAAAGGGCTTACCCGGCCAGGCTCGGAGAACCCGTTCCCTCGCGAGCCCGCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:42397180..42397281 26863196 MeRIP-seq:(Medium) rs902571882 Functional Loss SNV dbSNP153 33..33 33 - - - 84687 RMVar_ID_84687 Human_SNP_ID_666339843 m1A Human chr19 + 42397325 42397325 42397325 AGTGAGGCTTGAGGCGGAGGGGGGAGGAGCTCAGTCCCGGCGAACCCATCTTGCTTTCTTGGAGA AGTGAGGCTTGAGGCGGAGGGGGGAGGAGCTCGGTCCCGGCGAACCCATCTTGCTTTCTTGGAGA A G LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42397321..42397437 26863196 MeRIP-seq:(Medium) rs375278890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20397514 84688 RMVar_ID_84688 Human_SNP_ID_666340209 m1A Human chr19 - 42398849 42398849 42398849 ATGCTGGACAACCCCTTGTCCCATAGCCCATCAATCCCCACTTTCTGTTCTCTCTGCCTCCTGAA ATGCTGGACAACCCCTTGTCCCATAGCCCATCGATCCCCACTTTCTGTTCTCTCTGCCTCCTGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42398807..42399016 26863196 MeRIP-seq:(Medium) rs1165985638 Functional Loss SNV dbSNP153 33..33 33 - - - 84689 RMVar_ID_84689 Human_SNP_ID_666376403 m1A Human chr19 + 42546972 42546972 42546972 CCAGGCTGCAGCTGGGGAGGGAAGATGTGGGGAGTAGTGGGTGAAGGGAGAAGCAGACTGTGATT CCAGGCTGCAGCTGGGGAGGGAAGATGTGGGGTGTAGTGGGTGAAGGGAGAAGCAGACTGTGATT A T LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42546928..42546993 26863196 MeRIP-seq:(Medium) rs971028538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5587772 84690 RMVar_ID_84690 Human_SNP_ID_666636445 m1A Human chr19 + 43324178 43324178 43324178 GGGGTTGTTAGAAGAAACATTTGTCATATAGTATGATTGGTGATGGCCTGGATACAGTTTTGTGT GGGGTTGTTAGAAGAAACATTTGTCATATAGTGTGATTGGTGATGGCCTGGATACAGTTTTGTGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:43324066..43324193 26863196 MeRIP-seq:(Medium) rs896692667 Functional Loss SNV dbSNP153 33..33 33 - - - 84691 RMVar_ID_84691 Human_SNP_ID_666636916 m1A Human chr19 + 43325526 43325526 43325526 AGAAAATAGATTTTGGAAGTTGAGAAATGTAGAGAGTGAGTTGAGCATAGTTTGTGATTTTCAGG AGAAAATAGATTTTGGAAGTTGAGAAATGTAGGGAGTGAGTTGAGCATAGTTTGTGATTTTCAGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:43325476..43325550 26863196 MeRIP-seq:(Medium) rs954747164 Functional Loss SNV dbSNP153 33..33 33 - - - 84692 RMVar_ID_84692 Human_SNP_ID_666637291 m1A Human chr19 + 43326456 43326456 43326456 GCTGTAGTCCAGGAATAGTCAGGGAAGCAGATAATTTACTTAAAGTGCCTCAGCCTAATAAGGGA GCTGTAGTCCAGGAATAGTCAGGGAAGCAGATGATTTACTTAAAGTGCCTCAGCCTAATAAGGGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:43326401..43326475 26863196 MeRIP-seq:(Medium) rs1262024103 Functional Loss SNV dbSNP153 33..33 33 - - - 84693 RMVar_ID_84693 Human_SNP_ID_666637465 m1A Human chr19 - 43326869 43326869 43326869 AAGCCGCGTCCCATCTGTGTGGGACCCCACTGAAAATCGGACTGTTCAACTCACCTGGCAGCCAC AAGCCGCGTCCCATCTGTGTGGGACCCCACTGGAAATCGGACTGTTCAACTCACCTGGCAGCCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:43326851..43326875 26863196 MeRIP-seq:(Medium) rs1216138153 Functional Loss SNV dbSNP153 33..33 33 - - - 84694 RMVar_ID_84694 Human_SNP_ID_666637525 m1A Human chr19 + 43327006 43327006 43327006 GGGAGGAGGTTCTGGAGGAACGCCTGGTTGCTATGGTTCAGGCGTTTGGAAGTTCTTGTGTGCTG GGGAGGAGGTTCTGGAGGAACGCCTGGTTGCTGTGGTTCAGGCGTTTGGAAGTTCTTGTGTGCTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:43327001..43327050 26863196 MeRIP-seq:(Medium) rs1030823745 Functional Loss SNV dbSNP153 33..33 33 - - - 84695 RMVar_ID_84695 Human_SNP_ID_666637910 m1A Human chr19 + 43328087 43328087 43328087 GGGATTGGGGTGCAGACATAAGAGGTTGGGGCATGGAAGTAAGGGATTGGGGCACAGAGATAACA GGGATTGGGGTGCAGACATAAGAGGTTGGGGCGTGGAAGTAAGGGATTGGGGCACAGAGATAACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43327976..43328281 26863196 MeRIP-seq:(Medium) rs1207674123 Functional Loss SNV dbSNP153 33..33 33 - - - 84696 RMVar_ID_84696 Human_SNP_ID_666638051 m1A Human chr19 + 43328401 43328401 43328401 CCCGGAAAAGCAGAGAAGGGGTAGAGACAAGGAGAGAAGGGTTGGGGTACTTGCCCCTTCCCCAG CCCGGAAAAGCAGAGAAGGGGTAGAGACAAGGGGAGAAGGGTTGGGGTACTTGCCCCTTCCCCAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:43328376..43328400 26863196 MeRIP-seq:(Medium) rs1195989229 Functional Loss SNV dbSNP153 33..33 33 - - - 84697 RMVar_ID_84697 Human_SNP_ID_666672940 m1A Human chr19 + 43461679 43461679 43461679 CAGTCGTGGGCTCTGGAGGGGGCAGCCGGACAAGGGGTGGGATTCGAGGGGAGAAGTAGGTCTTG CAGTCGTGGGCTCTGGAGGGGGCAGCCGGACAGGGGGTGGGATTCGAGGGGAGAAGTAGGTCTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43461629..43461765 26863196 MeRIP-seq:(Medium) rs1379671280 Functional Loss SNV dbSNP153 33..33 33 - - - 84698 RMVar_ID_84698 Human_SNP_ID_666674230 m1A Human chr19 - 43465556 43465556 43465556 GGGAGCAGGACGGAGCCATGGACCCCGCCAGGAAAGCAGGTGCCCAGGCCATGATCTGGACTGCA GGGAGCAGGACGGAGCCATGGACCCCGCCAGGGAAGCAGGTGCCCAGGCCATGATCTGGACTGCA T C LYPD3 Ensembl:ENSG00000124466 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:43464326..43465655 26863196 MeRIP-seq:(Medium) rs776589153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2015331,Human_Splice_Rec_2015339,Human_Splice_Rec_2015349 RMVar_hsa_circ_195141,RMVar_hsa_circ_106514 84699 RMVar_ID_84699 Human_SNP_ID_666674238 m1A Human chr19 - 43465567 43465567 43465567 GGGGACGCCAAGGGAGCAGGACGGAGCCATGGACCCCGCCAGGAAAGCAGGTGCCCAGGCCATGA GGGGACGCCAAGGGAGCAGGACGGAGCCATGGGCCCCGCCAGGAAAGCAGGTGCCCAGGCCATGA T C LYPD3 Ensembl:ENSG00000124466 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43465498..43465583 26863196 MeRIP-seq:(Medium) rs766605659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2015331,Human_Splice_Rec_2015339,Human_Splice_Rec_2015349 RMVar_hsa_circ_195141,RMVar_hsa_circ_106514 84700 RMVar_ID_84700 Human_SNP_ID_666676559 m1A Human chr19 + 43475250 43475250 43475250 GTCGGGGGCAAGGCACCTGCAACCCAGAACGCAGCAGCTCAGGCCAGCTGAACTGCCGCGCCTGC GTCGGGGGCAAGGCACCTGCAACCCAGAACGCGGCAGCTCAGGCCAGCTGAACTGCCGCGCCTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43475200..43475399 32194978 MeRIP-seq:(Medium) rs1174912983 Functional Loss SNV dbSNP153 33..33 33 - - - 84701 RMVar_ID_84701 Human_SNP_ID_666682550 m1A Human chr19 - 43497279 43497279 43497279 GGCCTCCACCCTTTTTGTGTTCCGACCTATAGATGAGGGAACAACTGGATGTGGCCCAACGTGCC GGCCTCCACCCTTTTTGTGTTCCGACCTATAGGTGAGGGAACAACTGGATGTGGCCCAACGTGCC T C PHLDB3 Ensembl:ENSG00000176531 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43497254..43497872 32194978 MeRIP-seq:(Medium) rs1486258910 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_908734,Human_RBP_ID_18995056,Human_RBP_ID_27816488 Human_Splice_Rec_2015378,Human_Splice_Rec_2015400,Human_Splice_Rec_2015432 RMVar_hsa_circ_293108,RMVar_hsa_circ_361383 84702 RMVar_ID_84702 Human_SNP_ID_666683887 m1A Human chr19 - 43501861 43501861 43501861 AGCCCTGGCATTCTCTCCGCAGATGGAGGTGGAGGTGGCCTTGCTGCGGGGTGAGCTGGCTGGGG AGCCCTGGCATTCTCTCCGCAGATGGAGGTGGGGGTGGCCTTGCTGCGGGGTGAGCTGGCTGGGG T C PHLDB3 Ensembl:ENSG00000176531 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43501722..43504130 26863196 MeRIP-seq:(Medium) rs758248549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908735,Human_RBP_ID_9353601,Human_RBP_ID_9382604,Human_RBP_ID_18998008,Human_RBP_ID_22662765 Human_Splice_Rec_2015374,Human_Splice_Rec_2015428,Human_Splice_Rec_2015438 RMVar_hsa_circ_100384,RMVar_hsa_circ_195144 84703 RMVar_ID_84703 Human_SNP_ID_666684624 m1A Human chr19 - 43504017 43504017 43504017 CAGCCCCAGGGCCATCCCGAGGAGTCCCGGGAACAGGAGGCATCCGAAGTCCTGGCGGAACCTTC CAGCCCCAGGGCCATCCCGAGGAGTCCCGGGAGCAGGAGGCATCCGAAGTCCTGGCGGAACCTTC T C PHLDB3 Ensembl:ENSG00000176531 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43503968..43504217 32194978 MeRIP-seq:(Medium) rs1230228460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24375982 84704 RMVar_ID_84704 Human_SNP_ID_666685440 m1A Human chr19 + 43506818 43506818 43506818 ATTGCCGCCCTCTCCTCCCACCTAGTGCATTAATAGTGGATGGGAGCATCTGACAGAAGTGAGAT ATTGCCGCCCTCTCCTCCCACCTAGTGCATTAGTAGTGGATGGGAGCATCTGACAGAAGTGAGAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:43506767..43507638 32194978 MeRIP-seq:(Medium) rs770386105 Functional Loss SNV dbSNP153 33..33 33 - - - 84705 RMVar_ID_84705 Human_SNP_ID_666685621 m1A Human chr19 - 43507237 43507237 43507237 ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGACTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGTCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG T A ETHE1 Ensembl:ENSG00000105755 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:43507154..43507335 26863196 MeRIP-seq:(Medium) rs12977609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89520,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_99105,RMVar_hsa_circ_195146,RMVar_hsa_circ_195148,RMVar_hsa_circ_89009,RMVar_hsa_circ_195149,RMVar_hsa_circ_195147,RMVar_hsa_circ_195151,RMVar_hsa_circ_195145,RMVar_hsa_circ_377331 84706 RMVar_ID_84706 Human_SNP_ID_666685622 m1A Human chr19 - 43507237 43507237 43507237 ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGACTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGGCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG T C ETHE1 Ensembl:ENSG00000105755 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:43507154..43507335 26863196 MeRIP-seq:(Medium) rs12977609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89520,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_99105,RMVar_hsa_circ_195146,RMVar_hsa_circ_195148,RMVar_hsa_circ_89009,RMVar_hsa_circ_195149,RMVar_hsa_circ_195147,RMVar_hsa_circ_195151,RMVar_hsa_circ_195145,RMVar_hsa_circ_377331 84707 RMVar_ID_84707 Human_SNP_ID_666685623 m1A Human chr19 - 43507237 43507237 43507237 ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGACTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG ACTCCTGAGTCTGAGGGAGGAGGGGCTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCTG T G ETHE1 Ensembl:ENSG00000105755 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:43507154..43507335 26863196 MeRIP-seq:(Medium) rs12977609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89520,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_99105,RMVar_hsa_circ_195146,RMVar_hsa_circ_195148,RMVar_hsa_circ_89009,RMVar_hsa_circ_195149,RMVar_hsa_circ_195147,RMVar_hsa_circ_195151,RMVar_hsa_circ_195145,RMVar_hsa_circ_377331 84708 RMVar_ID_84708 Human_SNP_ID_666685728 m1A Human chr19 - 43507486 43507486 43507486 CTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGAACTGGGGGCCTGGACTCCTGGATCTGAGG CTGGGGGCCTGGACTCCTGGGTCTGAGGGAGGGGGAACTGGGGGCCTGGACTCCTGGATCTGAGG T C ETHE1 Ensembl:ENSG00000105755 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43507139..43507768 26863196 MeRIP-seq:(Medium) rs1177551943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21978028 RMVar_hsa_circ_89520,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_99105,RMVar_hsa_circ_195146,RMVar_hsa_circ_195148,RMVar_hsa_circ_89009,RMVar_hsa_circ_195149,RMVar_hsa_circ_195147,RMVar_hsa_circ_195151,RMVar_hsa_circ_195145,RMVar_hsa_circ_377331 84709 RMVar_ID_84709 Human_SNP_ID_666690781 m1A Human chr19 + 43526558 43526558 43526558 AGCCGCAGCCCCAGCTCCTTGATCAGCTGGGCATCCCGAGGCGCTGTTTCCAGGACTGGGTCGAT AGCCGCAGCCCCAGCTCCTTGATCAGCTGGGCTTCCCGAGGCGCTGTTTCCAGGACTGGGTCGAT A T ZNF575 Ensembl:ENSG00000176472 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43526526..43527147 32194978 MeRIP-seq:(Medium) rs766622906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2015495 84710 RMVar_ID_84710 Human_SNP_ID_666690806 m1A Human chr19 - 43526628 43526628 43526628 GATGTTCGAGCCTGTGAGCTGCACCTTCACGTACCTGCTGGGTGACAGAGAGTCCCGGGAGGCCG GATGTTCGAGCCTGTGAGCTGCACCTTCACGTGCCTGCTGGGTGACAGAGAGTCCCGGGAGGCCG T C ETHE1 Ensembl:ENSG00000105755 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43526577..43526953 26863196 MeRIP-seq:(Medium) rs1555765564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558518 Human_Splice_Rec_2015446,Human_Splice_Rec_2015458,Human_Splice_Rec_2015468,Human_Splice_Rec_2015478,Human_Splice_Rec_2015486,Human_Splice_Rec_2015492 Human_miRNA_ID_2223976,Human_miRNA_ID_2487046,Human_miRNA_ID_3075412 Clinvar_Rec_439 GWAS_ID_10115 RMVar_hsa_circ_8764,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_195146,RMVar_hsa_circ_195145,RMVar_hsa_circ_273510,RMVar_hsa_circ_90710,RMVar_hsa_circ_195152,RMVar_hsa_circ_195153 84711 RMVar_ID_84711 Human_SNP_ID_666693395 m1A Human chr19 + 43535187 43535187 43535187 ACAAGGCCTTCTCGTACCCGTCCAAGCTGGCCACGCACCGCTTAGCACACGGAGGCGCCCGACCC ACAAGGCCTTCTCGTACCCGTCCAAGCTGGCCGCGCACCGCTTAGCACACGGAGGCGCCCGACCC A G ZNF575 Ensembl:ENSG00000176472 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43534413..43535585 26863196 MeRIP-seq:(Medium) rs866347256 Functional Loss SNV dbSNP153 33..33 33 - - - 84712 RMVar_ID_84712 Human_SNP_ID_666693455 m1A Human chr19 - 43535281 43535281 43535281 GGCACGGGTGCGGGCGGGCGCCGCTGTGCGTGAGGCGGTGGGCTGCCAGCTTGGAGGGGTAGGAG GGCACGGGTGCGGGCGGGCGCCGCTGTGCGTGTGGCGGTGGGCTGCCAGCTTGGAGGGGTAGGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:43535088..43535549 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 84713 RMVar_ID_84713 Human_SNP_ID_666696290 m1A Human chr19 - 43545901 43545900 43545901 ACTGCCCCCTGGCCAGGAGGAGAATGGGGAAGACCCGTATGCAGGCTCCACGGATGAGAACACGG ACTGCCCCCTGGCCAGGAGGAGAATGGGGAAG_CCCGTATGCAGGCTCCACGGATGAGAACACGG GT G XRCC1 Ensembl:ENSG00000073050 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43545851..43546125 26863196 MeRIP-seq:(Medium) rs1381635867 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1888652,Human_RBP_ID_3955155,Human_RBP_ID_4533403,Human_RBP_ID_18998010,Human_RBP_ID_22973662 Human_Splice_Rec_2015544,Human_Splice_Rec_2015545,Human_Splice_Rec_2015574,Human_Splice_Rec_2015575 Human_miRNA_ID_2158124 RMVar_hsa_circ_108246,RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195155,RMVar_hsa_circ_195159,RMVar_hsa_circ_195158,RMVar_hsa_circ_326144 84714 RMVar_ID_84714 Human_SNP_ID_666696297 m1A Human chr19 + 43545924 43545924 43545924 GCATACGGGTCTTCCCCATTCTCCTCCTGGCCAGGGGGCAGTCTGTGTTCCTTCTGCTCTGCCAC GCATACGGGTCTTCCCCATTCTCCTCCTGGCCGGGGGGCAGTCTGTGTTCCTTCTGCTCTGCCAC A G lnc-PINLYP-4 RNACentral:URS00009C5D69 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43545876..43546043 26863196 MeRIP-seq:(Medium) rs773481172 Functional Loss SNV dbSNP153 33..33 33 - - - 84715 RMVar_ID_84715 Human_SNP_ID_666696298 m1A Human chr19 + 43545924 43545924 43545924 GCATACGGGTCTTCCCCATTCTCCTCCTGGCCAGGGGGCAGTCTGTGTTCCTTCTGCTCTGCCAC GCATACGGGTCTTCCCCATTCTCCTCCTGGCCTGGGGGCAGTCTGTGTTCCTTCTGCTCTGCCAC A T lnc-PINLYP-4 RNACentral:URS00009C5D69 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43545876..43546043 26863196 MeRIP-seq:(Medium) rs773481172 Functional Loss SNV dbSNP153 33..33 33 - - - 84716 RMVar_ID_84716 Human_SNP_ID_666696548 m1A Human chr19 - 43546644 43546644 43546644 CAGAAGCCCCCAACCCCTGAAGAGACCAAAGCAGCCTCACCAGTGCTCCAGGAAGATATAGACAT CAGAAGCCCCCAACCCCTGAAGAGACCAAAGCTGCCTCACCAGTGCTCCAGGAAGATATAGACAT T A XRCC1 Ensembl:ENSG00000073050 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:43546560..43546725 26863196 MeRIP-seq:(Medium) rs920813182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522969 Human_Splice_Rec_2015540,Human_Splice_Rec_2015541,Human_Splice_Rec_2015570,Human_Splice_Rec_2015571 Human_miRNA_ID_2716375,Human_miRNA_ID_3052360 RMVar_hsa_circ_108246,RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195155,RMVar_hsa_circ_195159,RMVar_hsa_circ_195158,RMVar_hsa_circ_326144 84717 RMVar_ID_84717 Human_SNP_ID_666696642 m1A Human chr19 - 43546906 43546906 43546906 TGAGGCCTCTCACAGCGGTGGCAGCGGAGATGAAGCCCCCAAGCTTCCTCAGAAGGTCTGATGCC TGAGGCCTCTCACAGCGGTGGCAGCGGAGATGGAGCCCCCAAGCTTCCTCAGAAGGTCTGATGCC T C XRCC1 Ensembl:ENSG00000073050 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43546655..43552228 32194978 MeRIP-seq:(Medium) rs1287459280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5371852,Human_RBP_ID_18998013 Human_Splice_Rec_2015538,Human_Splice_Rec_2015539,Human_Splice_Rec_2015568,Human_Splice_Rec_2015569 RMVar_hsa_circ_18280,RMVar_hsa_circ_108246,RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195155,RMVar_hsa_circ_195159,RMVar_hsa_circ_195158,RMVar_hsa_circ_326144,RMVar_hsa_circ_119776,RMVar_hsa_circ_195160 84718 RMVar_ID_84718 Human_SNP_ID_666698257 m1A Human chr19 - 43552229 43552229 43552229 CGTACCCCAGCCACAGCCCCAGTCCCTGCCCGAGCACAGGGGGCAGTGACAGGCAAACCCCGAGG CGTACCCCAGCCACAGCCCCAGTCCCTGCCCGCGCACAGGGGGCAGTGACAGGCAAACCCCGAGG T G XRCC1 Ensembl:ENSG00000073050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:43552178..43552897 32194978 MeRIP-seq:(Medium) rs1198109417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2015534,Human_Splice_Rec_2015564,Human_Splice_Rec_2015590,Human_Splice_Rec_2015606,Human_Splice_Rec_2015614,Human_Splice_Rec_2015630 RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_59391,RMVar_hsa_circ_115456,RMVar_hsa_circ_195161 84719 RMVar_ID_84719 Human_SNP_ID_666698513 m1A Human chr19 - 43552858 43552858 43552858 GGGAAGAGGAAGTTGGATTTGAACCAAGAAGAAAAGAAGACCCCCAGCAAACCACCAGCCCAGCT GGGAAGAGGAAGTTGGATTTGAACCAAGAAGAGAAGAAGACCCCCAGCAAACCACCAGCCCAGCT T C XRCC1 Ensembl:ENSG00000073050 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43552792..43553037 26863196 MeRIP-seq:(Medium) rs200575088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911505,Human_RBP_ID_1566539,Human_RBP_ID_1888656,Human_RBP_ID_3572739,Human_RBP_ID_8256187 Human_Splice_Rec_2015532,Human_Splice_Rec_2015533,Human_Splice_Rec_2015562,Human_Splice_Rec_2015563,Human_Splice_Rec_2015589,Human_Splice_Rec_2015605,Human_Splice_Rec_2015612,Human_Splice_Rec_2015613,Human_Splice_Rec_2015628,Human_Splice_Rec_2015629 Human_miRNA_ID_2158125,Human_miRNA_ID_2686271 RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_59391,RMVar_hsa_circ_115456,RMVar_hsa_circ_195161,RMVar_hsa_circ_99505,RMVar_hsa_circ_195162 84720 RMVar_ID_84720 Human_SNP_ID_666701424 m1A Human chr19 - 43563660 43563660 43563660 AGCTATGGATATGTTTGAGGGAAGAGTGGTCTAGGCAGGGGGATTGGCAGGTGCAGAGGCCCTGA AGCTATGGATATGTTTGAGGGAAGAGTGGTCTGGGCAGGGGGATTGGCAGGTGCAGAGGCCCTGA T C L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43563656..43563845 26863196 MeRIP-seq:(Medium) rs976371121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13466638 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 84721 RMVar_ID_84721 Human_SNP_ID_666703258 m1A Human chr19 + 43571052 43571052 43571052 GATTGTCAACATGGAGCCAGCAGGATCCTGTGAAGGCCTAAGGCAGATCCTGTCCCTCCTCTGCT GATTGTCAACATGGAGCCAGCAGGATCCTGTGGAGGCCTAAGGCAGATCCTGTCCCTCCTCTGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43571050..43571273 26863196 MeRIP-seq:(Medium) rs934223377 Functional Loss SNV dbSNP153 33..33 33 - - - 84722 RMVar_ID_84722 Human_SNP_ID_666703447 m1A Human chr19 - 43571995 43571995 43571995 GACTTTGGGACATTCTAGGGGTGGCATCCAGGAGGCAGTTGGGGATCACATGTGGAGCTGAAGAC GACTTTGGGACATTCTAGGGGTGGCATCCAGGCGGCAGTTGGGGATCACATGTGGAGCTGAAGAC T G L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43571994..43572131 26863196 MeRIP-seq:(Medium) rs797008604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6767780,Human_RBP_ID_13466855 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 84723 RMVar_ID_84723 Human_SNP_ID_666704155 m1A Human chr19 - 43574969 43574969 43574969 CTCACTGTGCAGAAAATCTTCTCAAGGCAGACACTTACCGAAAATGGCGGGCAGCCAAGGCAGGC CTCACTGTGCAGAAAATCTTCTCAAGGCAGACGCTTACCGAAAATGGCGGGCAGCCAAGGCAGGC T C L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:43574919..43575473 32194978 MeRIP-seq:(Medium) rs775976174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908738,Human_RBP_ID_1888675,Human_RBP_ID_9088326 Human_Splice_Rec_2015520,Human_Splice_Rec_2015521,Human_Splice_Rec_2015594,Human_Splice_Rec_2015595,Human_Splice_Rec_2015616,Human_Splice_Rec_2015617,Human_Splice_Rec_2015642,Human_Splice_Rec_2015643,Human_Splice_Rec_2015652 Human_miRNA_ID_2455898 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 84724 RMVar_ID_84724 Human_SNP_ID_666704156 m1A Human chr19 - 43574969 43574969 43574969 CTCACTGTGCAGAAAATCTTCTCAAGGCAGACACTTACCGAAAATGGCGGGCAGCCAAGGCAGGC CTCACTGTGCAGAAAATCTTCTCAAGGCAGACCCTTACCGAAAATGGCGGGCAGCCAAGGCAGGC T G L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:43574919..43575473 32194978 MeRIP-seq:(Medium) rs775976174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908738,Human_RBP_ID_1888675,Human_RBP_ID_9088326 Human_Splice_Rec_2015520,Human_Splice_Rec_2015521,Human_Splice_Rec_2015594,Human_Splice_Rec_2015595,Human_Splice_Rec_2015616,Human_Splice_Rec_2015617,Human_Splice_Rec_2015642,Human_Splice_Rec_2015643,Human_Splice_Rec_2015652 Human_miRNA_ID_2455898 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 84725 RMVar_ID_84725 Human_SNP_ID_666708104 m1A Human chr19 - 43590980 43590980 43590980 GGTGGTCCCACAAAAATGAGGTGAGGTGGGTAAGAGGTCTGGGCATGGTGGGCTCTGGGAGTAGC GGTGGTCCCACAAAAATGAGGTGAGGTGGGTAGGAGGTCTGGGCATGGTGGGCTCTGGGAGTAGC T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43590930..43591056 26863196 MeRIP-seq:(Medium) rs973658792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5321710,Human_RBP_ID_6767947,Human_RBP_ID_8198881,Human_RBP_ID_8834732,Human_RBP_ID_9353744,Human_RBP_ID_13467182,Human_RBP_ID_17926335,Human_RBP_ID_22477498,Human_RBP_ID_26472588 RMVar_hsa_circ_195166 84726 RMVar_ID_84726 Human_SNP_ID_666708375 m1A Human chr19 + 43591994 43591993 43591995 GCACCCAGGATTAAGCCCAGGCATCCCCTGTCAGAGTCTGGACTCCCAAGCCCCCTCCCACTCCT GCACCCAGGATTAAGCCCAGGCATCCCCTGTC__AGTCTGGACTCCCAAGCCCCCTCCCACTCCT CAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43591943..43592094 32194978 MeRIP-seq:(Medium) rs769347037 Functional Loss DEL dbSNP153 33..34 33 - - - 84727 RMVar_ID_84727 Human_SNP_ID_666708475 m1A Human chr19 - 43592224 43592224 43592224 CCAGGCCCGGTGACGCGCGCCGAGGTGGAAGCAAGACTGGGCGCCTGGGCGGGCGAGGGCACTGC CCAGGCCCGGTGACGCGCGCCGAGGTGGAAGCGAGACTGGGCGCCTGGGCGGGCGAGGGCACTGC T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43592099..43592464 26863196 MeRIP-seq:(Medium) rs1568527358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773088,Human_RBP_ID_4533641,Human_RBP_ID_5088824,Human_RBP_ID_18461969 Human_miRNA_ID_1265203 84728 RMVar_ID_84728 Human_SNP_ID_666708485 m1A Human chr19 - 43592244 43592244 43592244 TGGCAGCGCGCGCTCATTTCCCAGGCCCGGTGACGCGCGCCGAGGTGGAAGCAAGACTGGGCGCC TGGCAGCGCGCGCTCATTTCCCAGGCCCGGTGGCGCGCGCCGAGGTGGAAGCAAGACTGGGCGCC T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43592193..43592692 32194978 MeRIP-seq:(Medium) rs1476165945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5088824,Human_RBP_ID_18441544 Human_miRNA_ID_1265203 84729 RMVar_ID_84729 Human_SNP_ID_666708746 m1A Human chr19 - 43592734 43592734 43592734 CAGAAAGCAGGCAGCGGGGAAGGTCCTGGGAAAGCTGGCAGCGAGGGTTTGCAGCAGGTTGTCGG CAGAAAGCAGGCAGCGGGGAAGGTCCTGGGAAGGCTGGCAGCGAGGGTTTGCAGCAGGTTGTCGG T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43592686..43593041 26863196 MeRIP-seq:(Medium) rs766377558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5320428,Human_RBP_ID_6767990,Human_RBP_ID_18461319,Human_RBP_ID_27275281 84730 RMVar_ID_84730 Human_SNP_ID_666709456 m1A Human chr19 - 43594980 43594980 43594980 GCTACTGGCTGTGCGGAACCTCCGTCCTGGGGATTCACAGACTGCCGCCCAGGCCCGTGATCAGA GCTACTGGCTGTGCGGAACCTCCGTCCTGGGGGTTCACAGACTGCCGCCCAGGCCCGTGATCAGA T C IRGQ Ensembl:ENSG00000167378 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43594929..43595279 32194978 MeRIP-seq:(Medium) rs1293549702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1016524,Human_RBP_ID_6768005,Human_RBP_ID_9293794 Human_miRNA_ID_657799 84731 RMVar_ID_84731 Human_SNP_ID_666709555 m1A Human chr19 - 43595211 43595211 43595211 GGAGACGCTCGAGGCCCCCGAGGGACGGCCGGACTCCGGGGTTCCCAGCCTAAGAGCTGCGGGCC GGAGACGCTCGAGGCCCCCGAGGGACGGCCGGGCTCCGGGGTTCCCAGCCTAAGAGCTGCGGGCC T C IRGQ Ensembl:ENSG00000167378 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43595167..43595294 26863196 MeRIP-seq:(Medium) rs1377820437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9293796,Human_RBP_ID_27275290 84732 RMVar_ID_84732 Human_SNP_ID_666712889 m1A Human chr19 - 43607746 43607746 43607746 GAGGAACCACCTCGGGCTGGGGAGGGCCGACCAGCTGGGCGGGAGGAGGAGGAGGAAGAGGAGGA GAGGAACCACCTCGGGCTGGGGAGGGCCGACCCGCTGGGCGGGAGGAGGAGGAGGAAGAGGAGGA T G ZNF428 Ensembl:ENSG00000131116 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43596601..43612207 26863196 MeRIP-seq:(Medium) rs1177613611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4533806,Human_RBP_ID_5116943,Human_RBP_ID_6768121,Human_RBP_ID_8199528,Human_RBP_ID_8256189,Human_RBP_ID_17068366 RMVar_hsa_circ_117824,RMVar_hsa_circ_195168 84733 RMVar_ID_84733 Human_SNP_ID_666713011 m1A Human chr19 - 43608018 43608018 43608018 AAGAAGATGAGGAGGAGGAGGAAGAGGAGACCACTGACGATCCTGAATATGATCCTGGCTACAAG AAGAAGATGAGGAGGAGGAGGAAGAGGAGACCCCTGACGATCCTGAATATGATCCTGGCTACAAG T G ZNF428 Ensembl:ENSG00000131116 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:43596601..43612150;chr19:43596601..43612050 26863196 MeRIP-seq:(Medium) rs749440602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240324,Human_RBP_ID_523039,Human_RBP_ID_1190358,Human_RBP_ID_1566636,Human_RBP_ID_1888716,Human_RBP_ID_4569835,Human_RBP_ID_6768124,Human_RBP_ID_13467496,Human_RBP_ID_23800031,Human_RBP_ID_26336366 Human_Splice_Rec_2015742,Human_Splice_Rec_2015748 Human_miRNA_ID_2766113 RMVar_hsa_circ_117824,RMVar_hsa_circ_195168 84734 RMVar_ID_84734 Human_SNP_ID_666716369 m1A Human chr19 - 43619583 43619583 43619583 CGCAGAGGCTGGGCGTGCAGCCGCCGCCGCAGAGCCGGAGCGGGGGCCGCCGGCGCCGGTGAGTG CGCAGAGGCTGGGCGTGCAGCCGCCGCCGCAGGGCCGGAGCGGGGGCCGCCGGCGCCGGTGAGTG T C ZNF428 Ensembl:ENSG00000131116 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:43619481..43619678 26863196 MeRIP-seq:(Medium) rs941025200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240326,Human_RBP_ID_4533855 Human_Splice_Rec_2015739,Human_Splice_Rec_2015743,Human_Splice_Rec_2015749 RMVar_hsa_circ_117824,RMVar_hsa_circ_195168 84735 RMVar_ID_84735 Human_SNP_ID_666716426 m1A Human chr19 - 43619698 43619698 43619698 CCGACGCGCATAGCCCCTCTTCCCACAGCGCTACAGGACTAGTCCGTCTCGCCGCGCAAGCGCCC CCGACGCGCATAGCCCCTCTTCCCACAGCGCTCCAGGACTAGTCCGTCTCGCCGCGCAAGCGCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43619647..43619868 26863196 MeRIP-seq:(Medium) rs181582435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5421610 RMVar_hsa_circ_117824,RMVar_hsa_circ_195168 84736 RMVar_ID_84736 Human_SNP_ID_666717633 m1A Human chr19 - 43624059 43624059 43624059 TCTACGGTTGGTTGGTTGTAGGGCTCGGAAAGAGGCGGGGCCTAGAGCCAGGGTAACGAGAGGGC TCTACGGTTGGTTGGTTGTAGGGCTCGGAAAGGGGCGGGGCCTAGAGCCAGGGTAACGAGAGGGC T C CADM4 Ensembl:ENSG00000105767 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43624053..43624138 26863196 MeRIP-seq:(Medium) rs1261357318 Functional Loss SNV dbSNP153 33..33 33 - - - 84737 RMVar_ID_84737 Human_SNP_ID_666726074 m1A Human chr19 - 43656762 43656762 43656762 GATTCTAGAAAGATTCAGCAGGCAGAATAGGCAGGGCTCAATGACTGGCTGCAGGGTGGGATAAG GATTCTAGAAAGATTCAGCAGGCAGAATAGGCGGGGCTCAATGACTGGCTGCAGGGTGGGATAAG T C PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43656760..43656913 26863196 MeRIP-seq:(Medium) rs1054714491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103041,RMVar_hsa_circ_327308,RMVar_hsa_circ_195169,RMVar_hsa_circ_119663,RMVar_hsa_circ_195174,RMVar_hsa_circ_195175,RMVar_hsa_circ_375520,RMVar_hsa_circ_195177 84738 RMVar_ID_84738 Human_SNP_ID_666726075 m1A Human chr19 - 43656762 43656762 43656762 GATTCTAGAAAGATTCAGCAGGCAGAATAGGCAGGGCTCAATGACTGGCTGCAGGGTGGGATAAG GATTCTAGAAAGATTCAGCAGGCAGAATAGGCCGGGCTCAATGACTGGCTGCAGGGTGGGATAAG T G PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43656760..43656913 26863196 MeRIP-seq:(Medium) rs1054714491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103041,RMVar_hsa_circ_327308,RMVar_hsa_circ_195169,RMVar_hsa_circ_119663,RMVar_hsa_circ_195174,RMVar_hsa_circ_195175,RMVar_hsa_circ_375520,RMVar_hsa_circ_195177 84739 RMVar_ID_84739 Human_SNP_ID_666726539 m1A Human chr19 + 43658840 43658840 43658840 CCCCTCAAAGAAAAATAACTACAAGGCCACCCACGTCTTCTCACACAAACTTCCATGAAAATGAA CCCCTCAAAGAAAAATAACTACAAGGCCACCCGCGTCTTCTCACACAAACTTCCATGAAAATGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43658837..43659004 26863196 MeRIP-seq:(Medium) rs746371289 Functional Loss SNV dbSNP153 33..33 33 - - - 84740 RMVar_ID_84740 Human_SNP_ID_666726547 m1A Human chr19 + 43658895 43658895 43658895 TGAAAATGAAAACACAAATTCTCACCATTGCCAACATAGCTGTTCATACCTAGAACACCTTTTCC TGAAAATGAAAACACAAATTCTCACCATTGCCTACATAGCTGTTCATACCTAGAACACCTTTTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43658893..43659030 26863196 MeRIP-seq:(Medium) rs1003940190 Functional Loss SNV dbSNP153 33..33 33 - - - 84741 RMVar_ID_84741 Human_SNP_ID_666728858 m1A Human chr19 + 43667632 43667632 43667632 CGTGGTCCTGCAGAGGTCCTGTCCCAGGGCGCACTCTTCCACACGGCAATCCCCGTTGGTCTTAC CGTGGTCCTGCAGAGGTCCTGTCCCAGGGCGCCCTCTTCCACACGGCAATCCCCGTTGGTCTTAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43667555..43667686 26863196 MeRIP-seq:(Medium) rs772169129 Functional Loss SNV dbSNP153 33..33 33 - - - 84742 RMVar_ID_84742 Human_SNP_ID_666729022 m1A Human chr19 + 43668158 43668158 43668158 TATACCGTCACTCCCAGTGCCCTAATGGAACTATCCCTCCACTCACTCCCCCTGGTTCTACCCGG TATACCGTCACTCCCAGTGCCCTAATGGAACTGTCCCTCCACTCACTCCCCCTGGTTCTACCCGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:43668037..43668166 26863196 MeRIP-seq:(Medium) rs1222196793 Functional Loss SNV dbSNP153 33..33 33 - - - 84743 RMVar_ID_84743 Human_SNP_ID_666729601 m1A Human chr19 + 43670119 43670119 43670119 GCAGCAGCAGCGGCAGCAGCGGCGGGTGACCCATGTCGCGAGGGCAGCTCCTGTGCGCGGGGTCC GCAGCAGCAGCGGCAGCAGCGGCGGGTGACCCGTGTCGCGAGGGCAGCTCCTGTGCGCGGGGTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43667676..43670379 26863196 MeRIP-seq:(Medium) rs1209692404 Functional Loss SNV dbSNP153 33..33 33 - - - 84744 RMVar_ID_84744 Human_SNP_ID_666729612 m1A Human chr19 - 43670140 43670140 43670140 AGAAGGAGAGAAGACGTGCAGGGACCCCGCGCACAGGAGCTGCCCTCGCGACATGGGTCACCCGC AGAAGGAGAGAAGACGTGCAGGGACCCCGCGCGCAGGAGCTGCCCTCGCGACATGGGTCACCCGC T C PLAUR Ensembl:ENSG00000011422 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:43668207..43670159 26863196 MeRIP-seq:(Medium) rs1220497931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2015771,Human_Splice_Rec_2015787,Human_Splice_Rec_2015797,Human_Splice_Rec_2015809,Human_Splice_Rec_2015843,Human_Splice_Rec_2015865,Human_Splice_Rec_2015873 Human_miRNA_ID_2250376 RMVar_hsa_circ_103041,RMVar_hsa_circ_195175 84745 RMVar_ID_84745 Human_SNP_ID_666747123 m1A Human chr19 - 43736859 43736859 43736859 ATCTCCTCAGACTCTCGCCCTCGTGCCATTCGAGTCAACTTCAGGCCTTCCCTGACCATCTAACA ATCTCCTCAGACTCTCGCCCTCGTGCCATTCGCGTCAACTTCAGGCCTTCCCTGACCATCTAACA T G SMG9 Ensembl:ENSG00000105771 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:43736851..43736984 26863196 MeRIP-seq:(Medium) rs1308913463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1888764,Human_RBP_ID_17082514,Human_RBP_ID_20400253,Human_RBP_ID_22973798 RMVar_hsa_circ_118945,RMVar_hsa_circ_56515,RMVar_hsa_circ_98178,RMVar_hsa_circ_195182,RMVar_hsa_circ_195181,RMVar_hsa_circ_101862,RMVar_hsa_circ_34652,RMVar_hsa_circ_195188 84746 RMVar_ID_84746 Human_SNP_ID_666750138 m1A Human chr19 + 43748050 43748050 43748050 TGCATGACGGAAGTGCTTGTCTCTTCGCTGGCATCCTGTGGTGAGGGAGGGCAGTTACTCATGAA TGCATGACGGAAGTGCTTGTCTCTTCGCTGGCTTCCTGTGGTGAGGGAGGGCAGTTACTCATGAA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43748005..43750695 32194978 MeRIP-seq:(Medium) rs1267010000 Functional Loss SNV dbSNP153 33..33 33 - - - 84747 RMVar_ID_84747 Human_SNP_ID_666750828 m1A Human chr19 - 43750558 43750558 43750558 TGAGTGTCTGGACCCAGGAGCAGCATTCATGTATCTATTTGGTTCCACGCACCTGCCATGTGCCA TGAGTGTCTGGACCCAGGAGCAGCATTCATGTGTCTATTTGGTTCCACGCACCTGCCATGTGCCA T C SMG9 Ensembl:ENSG00000105771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43750556..43750679 26863196 MeRIP-seq:(Medium) rs908365316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5261580 RMVar_hsa_circ_118945,RMVar_hsa_circ_195181,RMVar_hsa_circ_195190,RMVar_hsa_circ_83060,RMVar_hsa_circ_308652,RMVar_hsa_circ_195192,RMVar_hsa_circ_195193,RMVar_hsa_circ_307067 84748 RMVar_ID_84748 Human_SNP_ID_666752065 m1A Human chr19 + 43754836 43754836 43754836 CACTCCGAAACCGGCCTCGGCGTCCGGGTTGCAGCCCCTAAGGAAAGCTGGGCCGAAGGAAGAAG CACTCCGAAACCGGCCTCGGCGTCCGGGTTGCGGCCCCTAAGGAAAGCTGGGCCGAAGGAAGAAG A G lnc-IRGC-5 RNACentral:URS0000D5D3B9 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:43754790..43754909 26863196 MeRIP-seq:(Medium) rs1019264955 Functional Loss SNV dbSNP153 33..33 33 - - - 84749 RMVar_ID_84749 Human_SNP_ID_666755047 m1A Human chr19 - 43766644 43766644 43766644 GGGCGGGGCTGGAGGTGGCGCCCCCTGGTGGGACAACAAAGAGGACACCATTTTTCCAGAGCTGC GGGCGGGGCTGGAGGTGGCGCCCCCTGGTGGGTCAACAAAGAGGACACCATTTTTCCAGAGCTGC T A KCNN4 Ensembl:ENSG00000104783 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43766593..43766788 26863196 MeRIP-seq:(Medium) rs201018803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330118,Human_RBP_ID_18165780,Human_RBP_ID_26472595 84750 RMVar_ID_84750 Human_SNP_ID_666755048 m1A Human chr19 - 43766644 43766644 43766644 GGGCGGGGCTGGAGGTGGCGCCCCCTGGTGGGACAACAAAGAGGACACCATTTTTCCAGAGCTGC GGGCGGGGCTGGAGGTGGCGCCCCCTGGTGGGGCAACAAAGAGGACACCATTTTTCCAGAGCTGC T C KCNN4 Ensembl:ENSG00000104783 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43766593..43766788 26863196 MeRIP-seq:(Medium) rs201018803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9330118,Human_RBP_ID_18165780,Human_RBP_ID_26472595 84751 RMVar_ID_84751 Human_SNP_ID_666755333 m1A Human chr19 - 43767709 43767709 43767709 GCCCCGACACCTCTGATCCTCTCCTCCCACCCAGATGCACATGATCCTGTATGACCTGCAGCAGA GCCCCGACACCTCTGATCCTCTCCTCCCACCCGGATGCACATGATCCTGTATGACCTGCAGCAGA T C KCNN4 Ensembl:ENSG00000104783 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43767678..43769083 32194978 MeRIP-seq:(Medium) rs1418457934 Functional Loss SNV dbSNP153 33..33 33 - - - 84752 RMVar_ID_84752 Human_SNP_ID_666757142 m1A Human chr19 + 43774589 43774589 43774589 CGCCGCCTGCCGCCCGGTCAGCGCCACGCGCCAGTCCCGCAGCCCGTTGTCGGTCATGAACAGCT CGCCGCCTGCCGCCCGGTCAGCGCCACGCGCCGGTCCCGCAGCCCGTTGTCGGTCATGAACAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43774538..43774641 26863196 MeRIP-seq:(Medium) rs772222937 Functional Loss SNV dbSNP153 33..33 33 - - - 84753 RMVar_ID_84753 Human_SNP_ID_666758332 m1A Human chr19 - 43778549 43778548 43778549 ACCAGTGAGAGATACACACACAGCGTTAGAAAAGACAATAGAGGGCCGGGCGCGGTGGCTCACGC ACCAGTGAGAGATACACACACAGCGTTAGAAA_GACAATAGAGGGCCGGGCGCGGTGGCTCACGC CT C KCNN4 Ensembl:ENSG00000104783 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43778547..43778722 26863196 MeRIP-seq:(Medium) rs770038155 Functional Loss DEL dbSNP153 33..33 33 - - - 84754 RMVar_ID_84754 Human_SNP_ID_666758333 m1A Human chr19 - 43778549 43778549 43778549 ACCAGTGAGAGATACACACACAGCGTTAGAAAAGACAATAGAGGGCCGGGCGCGGTGGCTCACGC ACCAGTGAGAGATACACACACAGCGTTAGAAATGACAATAGAGGGCCGGGCGCGGTGGCTCACGC T A KCNN4 Ensembl:ENSG00000104783 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43778547..43778722 26863196 MeRIP-seq:(Medium) rs139025582 Functional Loss SNV dbSNP153 33..33 33 - - - 84755 RMVar_ID_84755 Human_SNP_ID_666759124 m1A Human chr19 + 43780931 43780931 43780931 CAGGGTCCCCCACCTCGCAGCACGCACAGGGCAGCCACTGTGGCTTGCAGGTCGTCAGCCTGCTC CAGGGTCCCCCACCTCGCAGCACGCACAGGGCGGCCACTGTGGCTTGCAGGTCGTCAGCCTGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:43780658..43781000;chr19:43780635..43780975 26863196 MeRIP-seq:(Medium) rs199972422 Functional Loss SNV dbSNP153 33..33 33 - - - 84756 RMVar_ID_84756 Human_SNP_ID_666759128 m1A Human chr19 - 43780937 43780937 43780937 CCAGCAGAGCAGGCTGACGACCTGCAAGCCACAGTGGCTGCCCTGTGCGTGCTGCGAGGTGGGGG CCAGCAGAGCAGGCTGACGACCTGCAAGCCACGGTGGCTGCCCTGTGCGTGCTGCGAGGTGGGGG T C KCNN4 Ensembl:ENSG00000104783 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43780672..43780975 26863196 MeRIP-seq:(Medium) rs980563068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4558528,Human_RBP_ID_18421582 84757 RMVar_ID_84757 Human_SNP_ID_666759208 m1A Human chr19 - 43781214 43781214 43781214 TCTGGGTGTGGTGAGTAGAGGTGTGTGTCACAAAGTACAGACCATTGTGTGTGACAAAGCCCATC TCTGGGTGTGGTGAGTAGAGGTGTGTGTCACAGAGTACAGACCATTGTGTGTGACAAAGCCCATC T C KCNN4 Ensembl:ENSG00000104783 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43781164..43781264 26863196 MeRIP-seq:(Medium) rs199522968 Functional Loss SNV dbSNP153 33..33 33 - - - 84758 RMVar_ID_84758 Human_SNP_ID_666759240 m1A Human chr19 + 43781325 43781324 43781325 GCACACAACACAACCTACACAGAGTGACTCACAACTCCCAGCAAGCTCTGAAACCCACAGCCACA GCACACAACACAACCTACACAGAGTGACTCAC_ACTCCCAGCAAGCTCTGAAACCCACAGCCACA CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43781274..43781403 26863196 MeRIP-seq:(Medium) rs942833679 Functional Loss DEL dbSNP153 33..33 33 - - - 84759 RMVar_ID_84759 Human_SNP_ID_666759626 m1A Human chr19 + 43782866 43782866 43782866 CACTGCCCTTGGCCTCATGCACACCCCTCTGCAAGGAACCTGCGGACACAACCCTCCCCCTCCTT CACTGCCCTTGGCCTCATGCACACCCCTCTGCGAGGAACCTGCGGACACAACCCTCCCCCTCCTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43782776..43782980 26863196 MeRIP-seq:(Medium) rs1332113001 Functional Loss SNV dbSNP153 33..33 33 - - - 84760 RMVar_ID_84760 Human_SNP_ID_666759896 m1A Human chr19 - 43783740 43783739 43783741 TGGAGAAAGGGACAGAGCGATGAGAGAGACACAGAGAGGCTAAGAGAGGCAGAGACAGAGAGACA TGGAGAAAGGGACAGAGCGATGAGAGAGACA__GAGAGGCTAAGAGAGGCAGAGACAGAGAGACA CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43783695..43783857 26863196 MeRIP-seq:(Medium) rs1188818835 Functional Loss DEL dbSNP153 32..33 33 - - - 84761 RMVar_ID_84761 Human_SNP_ID_666762922 m1A Human chr19 - 43796129 43796129 43796129 GCCTTTGGGAGGTGGTGAGATCATGAGGGTGGAGCCCCCATGAATAGGATTAGTGCCCTTATAAA GCCTTTGGGAGGTGGTGAGATCATGAGGGTGGGGCCCCCATGAATAGGATTAGTGCCCTTATAAA T C LYPD5 Ensembl:ENSG00000159871 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43796078..43796179 32194978 MeRIP-seq:(Medium) rs977613543 Functional Loss SNV dbSNP153 33..33 33 - - - 84762 RMVar_ID_84762 Human_SNP_ID_666763319 m1A Human chr19 - 43797793 43797793 43797793 TTTCTCAGTCCCTGTGTACATCAGAACCTGCCACCGGCCCTCCTGCACCACCGAGGGCACCACCA TTTCTCAGTCCCTGTGTACATCAGAACCTGCCGCCGGCCCTCCTGCACCACCGAGGGCACCACCA T C LYPD5 Ensembl:ENSG00000159871 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43797709..43798640 32194978 MeRIP-seq:(Medium) rs1251070845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2016112,Human_Splice_Rec_2016122,Human_Splice_Rec_2016130,Human_Splice_Rec_2016136,Human_Splice_Rec_2016138,Human_Splice_Rec_2016142 84763 RMVar_ID_84763 Human_SNP_ID_666763835 m1A Human chr19 - 43798928 43798928 43798928 GAAGGGCTGCTGGACCGGGCCTCCTGCGGGCCAGACGCAATCGAACGCGGACGCGCTGCCGCCAG GAAGGGCTGCTGGACCGGGCCTCCTGCGGGCCGGACGCAATCGAACGCGGACGCGCTGCCGCCAG T C LYPD5 Ensembl:ENSG00000159871 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43798888..43799010 32194978 MeRIP-seq:(Medium) rs536675872 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_2016108,Human_Splice_Rec_2016118,Human_Splice_Rec_2016126,Human_Splice_Rec_2016132,Human_Splice_Rec_2016146,Human_Splice_Rec_2016152 84764 RMVar_ID_84764 Human_SNP_ID_666848795 m1A Human chr19 + 44165141 44165141 44165141 AGCAGCCATCTTTTCCCTGGCTTTGGTGATTCAGGTCAGCTTCTCAGGAACCTTTCAAACTTCCC AGCAGCCATCTTTTCCCTGGCTTTGGTGATTCGGGTCAGCTTCTCAGGAACCTTTCAAACTTCCC A G ZNF226 Ensembl:ENSG00000167380 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44165137..44165265 26863196 MeRIP-seq:(Medium) rs1487186354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18735129,Human_RBP_ID_19093580 Human_Splice_Rec_2016673,Human_Splice_Rec_2016683,Human_Splice_Rec_2016693,Human_Splice_Rec_2016703,Human_Splice_Rec_2016711,Human_Splice_Rec_2016721,Human_Splice_Rec_2016731,Human_Splice_Rec_2016739,Human_Splice_Rec_2016749,Human_Splice_Rec_2016761,Human_Splice_Rec_2016771,Human_Splice_Rec_2016781,Human_Splice_Rec_2016789,Human_Splice_Rec_2016801,Human_Splice_Rec_2016809 84765 RMVar_ID_84765 Human_SNP_ID_666851777 m1A Human chr19 + 44176325 44176325 44176325 TCAGTCGTAGATCAGCACTTAATGTTCATTGCAAGGTCCACACGGCAGAGAAACCTTATAATTGT TCAGTCGTAGATCAGCACTTAATGTTCATTGCCAGGTCCACACGGCAGAGAAACCTTATAATTGT A C ZNF226 Ensembl:ENSG00000167380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:44176299..44176420 32194978 MeRIP-seq:(Medium) rs1406513830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1567714,Human_RBP_ID_1889567,Human_RBP_ID_18735185,Human_RBP_ID_25423118 84766 RMVar_ID_84766 Human_SNP_ID_666851778 m1A Human chr19 + 44176325 44176325 44176325 TCAGTCGTAGATCAGCACTTAATGTTCATTGCAAGGTCCACACGGCAGAGAAACCTTATAATTGT TCAGTCGTAGATCAGCACTTAATGTTCATTGCGAGGTCCACACGGCAGAGAAACCTTATAATTGT A G ZNF226 Ensembl:ENSG00000167380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:44176299..44176420 32194978 MeRIP-seq:(Medium) rs1406513830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1567714,Human_RBP_ID_1889567,Human_RBP_ID_18735185,Human_RBP_ID_25423118 84767 RMVar_ID_84767 Human_SNP_ID_666860441 m1A Human chr19 - 44212587 44212587 44212587 CAAGAGGGGTCGTGGGGGTGCAGGGCTGACTCACCTCCCGGACCCAAAAGATGGTGGCGGCCTCG CAAGAGGGGTCGTGGGGGTGCAGGGCTGACTCCCCTCCCGGACCCAAAAGATGGTGGCGGCCTCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44212578..44212649 26863196 MeRIP-seq:(Medium) rs1023736756 Functional Loss SNV dbSNP153 33..33 33 - - - 84768 RMVar_ID_84768 Human_SNP_ID_666860567 m1A Human chr19 - 44213072 44213069 44213072 CCCGATGACTCAATCCTTCTTAAAAAAAAAAAAGATCTGTAAAAGTTCGGGAAGAGCTCGGTCTC CCCGATGACTCAATCCTTCTTAAAAAAAAAAA___TCTGTAAAAGTTCGGGAAGAGCTCGGTCTC ATCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44213069..44213186 26863196 MeRIP-seq:(Medium) rs757413910 Functional Loss DEL dbSNP153 33..35 33 - - - 84769 RMVar_ID_84769 Human_SNP_ID_666860570 m1A Human chr19 - 44213072 44213071 44213072 CCCGATGACTCAATCCTTCTTAAAAAAAAAAAAGATCTGTAAAAGTTCGGGAAGAGCTCGGTCTC CCCGATGACTCAATCCTTCTTAAAAAAAAAAA_GATCTGTAAAAGTTCGGGAAGAGCTCGGTCTC CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44213069..44213186 26863196 MeRIP-seq:(Medium) rs113556930 Functional Loss DEL dbSNP153 33..33 33 - - - 84770 RMVar_ID_84770 Human_SNP_ID_666933426 m1A Human chr19 - 44495501 44495501 44495501 TGTGTTGGGGGTCAGGTGCAGCCTGGTGTGGCATGTCAGAGCATGAGCATGTTGAGGGCATCATG TGTGTTGGGGGTCAGGTGCAGCCTGGTGTGGCGTGTCAGAGCATGAGCATGTTGAGGGCATCATG T C ZNF180 Ensembl:ENSG00000167384 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44495092..44495645 26863196 MeRIP-seq:(Medium) rs146132981 Functional Loss SNV dbSNP153 33..33 33 - - - 84771 RMVar_ID_84771 Human_SNP_ID_666934690 m1A Human chr19 - 44500478 44500478 44500478 ATTGTCCCGCGCGCGGACGCTTGCTGTCGCCGAGCAGCTCGGCCCTTCAGACTTAACCCCCAGCG ATTGTCCCGCGCGCGGACGCTTGCTGTCGCCGGGCAGCTCGGCCCTTCAGACTTAACCCCCAGCG T C ZNF180 Ensembl:ENSG00000167384 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44500428..44500493 26863196 MeRIP-seq:(Medium) rs1359412510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4570178 84772 RMVar_ID_84772 Human_SNP_ID_666971711 m1A Human chr19 - 44642493 44642493 44642493 ACACACTCAGAGATAAGGGCTGGGAGACAGAGACAGAGAGATTGAAAGAGATAGAGACACAGCAT ACACACTCAGAGATAAGGGCTGGGAGACAGAGTCAGAGAGATTGAAAGAGATAGAGACACAGCAT T A AC243964.3 Ensembl:ENSG00000266903 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44642453..44642567 26863196 MeRIP-seq:(Medium) rs557583003 Functional Loss SNV dbSNP153 33..33 33 - - - 84773 RMVar_ID_84773 Human_SNP_ID_666975287 m1A Human chr19 + 44654215 44654215 44654215 GGGAAGAGGGGCTGGGGGTCTGGACCCCTGGGACTGAGAGAGGAGGGGCTGGGCCTGGACCCCTG GGGAAGAGGGGCTGGGGGTCTGGACCCCTGGGTCTGAGAGAGGAGGGGCTGGGCCTGGACCCCTG A T PVR Ensembl:ENSG00000073008 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44654047..44654345 26863196 MeRIP-seq:(Medium) rs1246870227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5376843 RMVar_hsa_circ_3719 84774 RMVar_ID_84774 Human_SNP_ID_666977615 m1A Human chr19 + 44663426 44663426 44663426 GAACAGAGAAGTGTGGGGAAGAGATAGGAACCAGCAGGATGGCAGGGGCAAAGGGCTCAAGGGTG GAACAGAGAAGTGTGGGGAAGAGATAGGAACCTGCAGGATGGCAGGGGCAAAGGGCTCAAGGGTG A T PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:44663276..44663512;chr19:44663251..44663522;chr19:44663276..44663515 26863196 MeRIP-seq:(Medium) rs753774122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241110,Human_RBP_ID_772957,Human_RBP_ID_6772824,Human_RBP_ID_8489886,Human_RBP_ID_22718375 Human_miRNA_ID_272579 84775 RMVar_ID_84775 Human_SNP_ID_666991628 m1A Human chr19 - 44713276 44713276 44713276 GGGAAAGTGAGTACCTGACATTTTCAGCTTCTAGAGAGGGAGGCAGTGCGTGTGTCATGGAAGCA GGGAAAGTGAGTACCTGACATTTTCAGCTTCTGGAGAGGGAGGCAGTGCGTGTGTCATGGAAGCA T C AC243964.3 Ensembl:ENSG00000266903 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44713260..44713335 26863196 MeRIP-seq:(Medium) rs575908797 Functional Loss SNV dbSNP153 33..33 33 - - - 84776 RMVar_ID_84776 Human_SNP_ID_667001471 m1A Human chr19 + 44748240 44748240 44748240 AGAGGCAGAGAGATGGTGACAGACACAAAGAGACAAAAGAGAGAGACAGAGACGGAACAGAGCAC AGAGGCAGAGAGATGGTGACAGACACAAAGAGGCAAAAGAGAGAGACAGAGACGGAACAGAGCAC A G BCL3 Ensembl:ENSG00000069399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44748161..44748339 26863196 MeRIP-seq:(Medium) rs1005818408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585761 84777 RMVar_ID_84777 Human_SNP_ID_667001474 m1A Human chr19 + 44748263 44748252 44748263 CACAAAGAGACAAAAGAGAGAGACAGAGACGGAACAGAGCACACAGAGACAAACGCGGGGTTGCG CACAAAGAGACAAAAGAGAGAG___________ACAGAGCACACAGAGACAAACGCGGGGTTGCG GACAGAGACGGA G BCL3 Ensembl:ENSG00000069399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44748058..44748370 26863196 MeRIP-seq:(Medium) rs1184520742 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_5585761 84778 RMVar_ID_84778 Human_SNP_ID_667001663 m1A Human chr19 - 44748792 44748792 44748792 CCTCGTCCATGGCCCCCGCGGGGCATCGGGGCATGGGGCCGCCGGGGACGGCGGCCGGAGAGCGG CCTCGTCCATGGCCCCCGCGGGGCATCGGGGCCTGGGGCCGCCGGGGACGGCGGCCGGAGAGCGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44748743..44748934 26863196 MeRIP-seq:(Medium) rs1018435742 Functional Loss SNV dbSNP153 33..33 33 - - - 84779 RMVar_ID_84779 Human_SNP_ID_667002324 m1A Human chr19 + 44751284 44751284 44751284 TCGGGCCATGGGCTCCCCGTTTCCTCTGGTGAACCTGCCTACACCCCTATACCCCATGATGTGCC TCGGGCCATGGGCTCCCCGTTTCCTCTGGTGAGCCTGCCTACACCCCTATACCCCATGATGTGCC A G BCL3 Ensembl:ENSG00000069399 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:44748515..44751413 26863196 MeRIP-seq:(Medium) rs1175941368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18946993 Human_Splice_Rec_2017592,Human_Splice_Rec_2017593,Human_Splice_Rec_2017608,Human_Splice_Rec_2017609,Human_Splice_Rec_2017623 RMVar_hsa_circ_84901,RMVar_hsa_circ_126736,RMVar_hsa_circ_195226,RMVar_hsa_circ_195228,RMVar_hsa_circ_106781,RMVar_hsa_circ_195227 84780 RMVar_ID_84780 Human_SNP_ID_667002336 m1A Human chr19 + 44751307 44751307 44751307 CTCTGGTGAACCTGCCTACACCCCTATACCCCATGATGTGCCCCATGGAACACCCCCTTTCTGCT CTCTGGTGAACCTGCCTACACCCCTATACCCCCTGATGTGCCCCATGGAACACCCCCTTTCTGCT A C BCL3 Ensembl:ENSG00000069399 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:44751177..44751375 26863196 MeRIP-seq:(Medium) rs768087111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18946993 Human_Splice_Rec_2017592,Human_Splice_Rec_2017593,Human_Splice_Rec_2017608,Human_Splice_Rec_2017609,Human_Splice_Rec_2017623 Human_miRNA_ID_2277224 RMVar_hsa_circ_84901,RMVar_hsa_circ_126736,RMVar_hsa_circ_195226,RMVar_hsa_circ_195228,RMVar_hsa_circ_106781,RMVar_hsa_circ_195227 84781 RMVar_ID_84781 Human_SNP_ID_667002337 m1A Human chr19 + 44751307 44751307 44751307 CTCTGGTGAACCTGCCTACACCCCTATACCCCATGATGTGCCCCATGGAACACCCCCTTTCTGCT CTCTGGTGAACCTGCCTACACCCCTATACCCCGTGATGTGCCCCATGGAACACCCCCTTTCTGCT A G BCL3 Ensembl:ENSG00000069399 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:44751177..44751375 26863196 MeRIP-seq:(Medium) rs768087111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18946993 Human_Splice_Rec_2017592,Human_Splice_Rec_2017593,Human_Splice_Rec_2017608,Human_Splice_Rec_2017609,Human_Splice_Rec_2017623 Human_miRNA_ID_2277224 RMVar_hsa_circ_84901,RMVar_hsa_circ_126736,RMVar_hsa_circ_195226,RMVar_hsa_circ_195228,RMVar_hsa_circ_106781,RMVar_hsa_circ_195227 84782 RMVar_ID_84782 Human_SNP_ID_667002348 m1A Human chr19 - 44751333 44751333 44751333 TCTGCACGGGTGGCCATGGCGATGTCAGCAGAAAGGGGGTGTTCCATGGGGCACATCATGGGGTA TCTGCACGGGTGGCCATGGCGATGTCAGCAGATAGGGGGTGTTCCATGGGGCACATCATGGGGTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:44751176..44751375 26863196 MeRIP-seq:(Medium) rs755444152 Functional Loss SNV dbSNP153 33..33 33 - - - 84783 RMVar_ID_84783 Human_SNP_ID_667004264 m1A Human chr19 + 44758436 44758436 44758436 CAGCCGCAGGGTGAGCCGGGGCAGCTGTGGACATGCCCCTTGCACACGTGTGTCCGCGGGCTGGT CAGCCGCAGGGTGAGCCGGGGCAGCTGTGGACGTGCCCCTTGCACACGTGTGTCCGCGGGCTGGT A G BCL3 Ensembl:ENSG00000069399 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44758431..44758535 26863196 MeRIP-seq:(Medium) rs1184683549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19090313 RMVar_hsa_circ_84901,RMVar_hsa_circ_99535,RMVar_hsa_circ_126736,RMVar_hsa_circ_195226,RMVar_hsa_circ_195228,RMVar_hsa_circ_106781,RMVar_hsa_circ_195227,RMVar_hsa_circ_362280,RMVar_hsa_circ_195229,RMVar_hsa_circ_116272,RMVar_hsa_circ_108665,RMVar_hsa_circ_113181,RMVar_hsa_circ_195230,RMVar_hsa_circ_89796,RMVar_hsa_circ_195231,RMVar_hsa_circ_195232,RMVar_hsa_circ_195233,RMVar_hsa_circ_94999,RMVar_hsa_circ_195234 84784 RMVar_ID_84784 Human_SNP_ID_667004678 m1A Human chr19 - 44759497 44759497 44759497 ATGGGGAAGGAAGGAAGAAATTGGGAGGAGCCATGGGGAATCCAGGGGGGTCCCTGGGGGGAGAC ATGGGGAAGGAAGGAAGAAATTGGGAGGAGCCGTGGGGAATCCAGGGGGGTCCCTGGGGGGAGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:44758701..44759625 26863196 MeRIP-seq:(Medium) rs150051050 Functional Loss SNV dbSNP153 33..33 33 - - - 84785 RMVar_ID_84785 Human_SNP_ID_667018500 m1A Human chr19 + 44809150 44809150 44809150 CGTGAACATGGAGCCCCCGGACGCACCGGCCCAGGCGCGCGGGGCCCCGCGGCTGCTGTTGCTCG CGTGAACATGGAGCCCCCGGACGCACCGGCCCTGGCGCGCGGGGCCCCGCGGCTGCTGTTGCTCG A T BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:44809101..44809240;chr19:44809101..44809239;chr19:44809119..44809223 26863196 MeRIP-seq:(Medium) rs1217592022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772960,Human_RBP_ID_4559681,Human_RBP_ID_18470599,Human_RBP_ID_22447806 Human_Splice_Rec_2017701,Human_Splice_Rec_2017727,Human_Splice_Rec_2017755,Human_Splice_Rec_2017757,Human_Splice_Rec_2017769 84786 RMVar_ID_84786 Human_SNP_ID_667019044 m1A Human chr19 + 44811280 44811280 44811280 TCTGTACCCCCGCTGGTGGAGGTGATGCGAGGAAAGTCTGTCATTCTGGACTGCACCCCTACGGG TCTGTACCCCCGCTGGTGGAGGTGATGCGAGGGAAGTCTGTCATTCTGGACTGCACCCCTACGGG A G BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44811195..44811395 26863196 MeRIP-seq:(Medium) rs1434388523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772961,Human_RBP_ID_4557554,Human_RBP_ID_18470600,Human_RBP_ID_22448783 Human_Splice_Rec_2017702,Human_Splice_Rec_2017703,Human_Splice_Rec_2017728,Human_Splice_Rec_2017729,Human_Splice_Rec_2017756,Human_Splice_Rec_2017758,Human_Splice_Rec_2017759,Human_Splice_Rec_2017770,Human_Splice_Rec_2017771 84787 RMVar_ID_84787 Human_SNP_ID_667019428 m1A Human chr19 - 44812393 44812392 44812393 TGCCTCCCTTCGGGGGATGCCCGAGGACACTTACCAAACACGTTGAGCCGCGCAGTGGCCTCAGC TGCCTCCCTTCGGGGGATGCCCGAGGACACTT_CCAAACACGTTGAGCCGCGCAGTGGCCTCAGC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44812385..44812482 26863196 MeRIP-seq:(Medium) rs764347755 Functional Loss DEL dbSNP153 33..33 33 - - - 84788 RMVar_ID_84788 Human_SNP_ID_667019429 m1A Human chr19 - 44812393 44812393 44812393 TGCCTCCCTTCGGGGGATGCCCGAGGACACTTACCAAACACGTTGAGCCGCGCAGTGGCCTCAGC TGCCTCCCTTCGGGGGATGCCCGAGGACACTTGCCAAACACGTTGAGCCGCGCAGTGGCCTCAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44812385..44812482 26863196 MeRIP-seq:(Medium) rs1318540634 Functional Loss SNV dbSNP153 33..33 33 - - - 84789 RMVar_ID_84789 Human_SNP_ID_667019750 m1A Human chr19 + 44813295 44813295 44813295 ACAGCCGGAACGGGAACCCGGCCCCCAAGATCACGTGGTATCGCAACGGGCAGCGCCTGGAGGTG ACAGCCGGAACGGGAACCCGGCCCCCAAGATCGCGTGGTATCGCAACGGGCAGCGCCTGGAGGTG A G BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44813251..44818600 32194978 MeRIP-seq:(Medium) rs1397120071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2017708,Human_Splice_Rec_2017709,Human_Splice_Rec_2017734,Human_Splice_Rec_2017735,Human_Splice_Rec_2017764,Human_Splice_Rec_2017765,Human_Splice_Rec_2017775 84790 RMVar_ID_84790 Human_SNP_ID_667020113 m1A Human chr19 + 44814210 44814210 44814210 GTGGGCAGCCCGTCCACCCCAGCAGGCTGGGTACGCGAGGGTGACACTGTCCAGCTGCTCTGCCG GTGGGCAGCCCGTCCACCCCAGCAGGCTGGGTTCGCGAGGGTGACACTGTCCAGCTGCTCTGCCG A T BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:44814136..44814213 26863196 MeRIP-seq:(Medium) rs1232533108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18470601,Human_RBP_ID_22447807 Human_Splice_Rec_2017712,Human_Splice_Rec_2017713,Human_Splice_Rec_2017738,Human_Splice_Rec_2017739,Human_Splice_Rec_2017768 84791 RMVar_ID_84791 Human_SNP_ID_667021239 m1A Human chr19 - 44818600 44818600 44818600 TCCAGCGTAGGGCAGGGGTGGGCAGGCCGTGCACGGAGCAGTTCACGACTGCACTGCTGTTTAGA TCCAGCGTAGGGCAGGGGTGGGCAGGCCGTGCCCGGAGCAGTTCACGACTGCACTGCTGTTTAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44818499..44818657 26863196 MeRIP-seq:(Medium) rs1346629942 Functional Loss SNV dbSNP153 33..33 33 - - - 84792 RMVar_ID_84792 Human_SNP_ID_667021372 m1A Human chr19 - 44818847 44818847 44818847 GGACCAGCAGCGTGAAGTTCTGGGTGCGGCTGAGGACCGGGACTGTGGGCAGGGAGGCCTCACAT GGACCAGCAGCGTGAAGTTCTGGGTGCGGCTGGGGACCGGGACTGTGGGCAGGGAGGCCTCACAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44818796..44818946 32194978 MeRIP-seq:(Medium) rs1472682112 Functional Loss SNV dbSNP153 33..33 33 - - - 84793 RMVar_ID_84793 Human_SNP_ID_667022155 m1A Human chr19 - 44820954 44820954 44820954 AGCAGGGCTGGTTCTCTGATGCCTGCAGCTCCAGGTCCAGGGACAGCCTCTAGGAGGTTCTTGGC AGCAGGGCTGGTTCTCTGATGCCTGCAGCTCCCGGTCCAGGGACAGCCTCTAGGAGGTTCTTGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:44820811..44821050;chr19:44820812..44821012 26863196 MeRIP-seq:(Medium) rs1196490474 Functional Loss SNV dbSNP153 33..33 33 - - - 84794 RMVar_ID_84794 Human_SNP_ID_667022265 m1A Human chr19 + 44821273 44821273 44821273 TTTTACCTCCCGCCTCCCCTGCTGGTCCCCCCACCTGACGTCTTGCTGCAGAGTCTGACACTGGA TTTTACCTCCCGCCTCCCCTGCTGGTCCCCCCCCCTGACGTCTTGCTGCAGAGTCTGACACTGGA A C BCAM Ensembl:ENSG00000187244 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44821170..44821370 32194978 MeRIP-seq:(Medium) rs1415545469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523362,Human_RBP_ID_772981,Human_RBP_ID_17656184,Human_RBP_ID_18945618 Human_miRNA_ID_1419767,Human_miRNA_ID_1703965 84795 RMVar_ID_84795 Human_SNP_ID_667022266 m1A Human chr19 + 44821273 44821273 44821273 TTTTACCTCCCGCCTCCCCTGCTGGTCCCCCCACCTGACGTCTTGCTGCAGAGTCTGACACTGGA TTTTACCTCCCGCCTCCCCTGCTGGTCCCCCCGCCTGACGTCTTGCTGCAGAGTCTGACACTGGA A G BCAM Ensembl:ENSG00000187244 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44821170..44821370 32194978 MeRIP-seq:(Medium) rs1415545469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523362,Human_RBP_ID_772981,Human_RBP_ID_17656184,Human_RBP_ID_18945618 Human_miRNA_ID_1419767,Human_miRNA_ID_1703965 84796 RMVar_ID_84796 Human_SNP_ID_667029019 m1A Human chr19 + 44845106 44845106 44845106 CGCAGAGACAAGAGACGCCGAGAGGGAGACACAGAGAAAGAGACAGGGACAGAGAGACACAGATA CGCAGAGACAAGAGACGCCGAGAGGGAGACACGGAGAAAGAGACAGGGACAGAGAGACACAGATA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44845057..44845168 26863196 MeRIP-seq:(Medium) rs1225389712 Functional Loss SNV dbSNP153 33..33 33 - - - 84797 RMVar_ID_84797 Human_SNP_ID_667029452 m1A Human chr19 + 44846474 44846474 44846474 CACCTACTAAACCGCCCAGCCGATCGGCCCCCACAGAGTGGCCCGCGGGCCTCCGGCCGGGCCCA CACCTACTAAACCGCCCAGCCGATCGGCCCCCCCAGAGTGGCCCGCGGGCCTCCGGCCGGGCCCA A C NECTIN2 Ensembl:ENSG00000130202 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:44846351..44865325 26863410 MeRIP-seq:(Medium) rs893711346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557559,Human_RBP_ID_22447819,Human_RBP_ID_26815975 RMVar_hsa_circ_122951,RMVar_hsa_circ_195240 84798 RMVar_ID_84798 Human_SNP_ID_667035666 m1A Human chr19 - 44870330 44870330 44870330 CTTCTCCCCTGACCATCGTGGAGCATCCAACAAGCCTCCCCACATCCTCCTGGCCGCCCTCCAAG CTTCTCCCCTGACCATCGTGGAGCATCCAACAGGCCTCCCCACATCCTCCTGGCCGCCCTCCAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44870324..44870458 26863196 MeRIP-seq:(Medium) rs569702662 Functional Loss SNV dbSNP153 33..33 33 - - - 84799 RMVar_ID_84799 Human_SNP_ID_667036114 m1A Human chr19 - 44872056 44872056 44872056 GCAGGTGACCGTGACACCATCTGCTCGGCCCGAGGGCACCAAGGTGAAGCGGCTGGTGACAGTGA GCAGGTGACCGTGACACCATCTGCTCGGCCCGCGGGCACCAAGGTGAAGCGGCTGGTGACAGTGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44846424..44874534 32194978 MeRIP-seq:(Medium) rs1233393837 Functional Loss SNV dbSNP153 33..33 33 - - - 84800 RMVar_ID_84800 Human_SNP_ID_667037786 m1A Human chr19 - 44878319 44878319 44878319 TCCTCCTCCTCACCCTCAGCAGGATGAAGGCCAAGGACCCCCCAGCCAGAAGCAGCAGCACCAGC TCCTCCTCCTCACCCTCAGCAGGATGAAGGCCCAGGACCCCCCAGCCAGAAGCAGCAGCACCAGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44878276..44878650 26863196 MeRIP-seq:(Medium) rs1376950657 Functional Loss SNV dbSNP153 33..33 33 - - - 84801 RMVar_ID_84801 Human_SNP_ID_667037916 m1A Human chr19 + 44878613 44878613 44878613 GGACGGCTCCCTCATCTCACGGCGGGCAGTTTATGTGTGACCTGGACACAGACAGAGACAGAGCC GGACGGCTCCCTCATCTCACGGCGGGCAGTTTGTGTGTGACCTGGACACAGACAGAGACAGAGCC A G NECTIN2 Ensembl:ENSG00000130202 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44878316..44878875 32194978 MeRIP-seq:(Medium) rs1431355538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23800805,Human_RBP_ID_27275485 Human_Splice_Rec_2017818 Human_miRNA_ID_2515382,Human_miRNA_ID_2540668 RMVar_hsa_circ_116355,RMVar_hsa_circ_10259,RMVar_hsa_circ_122951,RMVar_hsa_circ_195240,RMVar_hsa_circ_77435,RMVar_hsa_circ_108054,RMVar_hsa_circ_195242,RMVar_hsa_circ_118252,RMVar_hsa_circ_195244,RMVar_hsa_circ_195243,RMVar_hsa_circ_195247 84802 RMVar_ID_84802 Human_SNP_ID_667040886 m1A Human chr19 + 44888961 44888961 44888961 GGGTCCAGACCCTTCCCTGAGCCCCCACCCCCACCCCAATTCCTGCCTACCAAGCAAGCAGCCCC GGGTCCAGACCCTTCCCTGAGCCCCCACCCCCCCCCCAATTCCTGCCTACCAAGCAAGCAGCCCC A C NECTIN2 Ensembl:ENSG00000130202 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1447955029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_523388,Human_RBP_ID_8198905 Human_miRNA_ID_1419771,Human_miRNA_ID_1703969 RMVar_hsa_circ_122951,RMVar_hsa_circ_195240,RMVar_hsa_circ_118252,RMVar_hsa_circ_195243,RMVar_hsa_circ_118992,RMVar_hsa_circ_195248 84803 RMVar_ID_84803 Human_SNP_ID_667041644 m1A Human chr19 + 44891301 44891301 44891301 CACGGGGTGGGAGCGGAGCCCAGGCCGGGAGCAGGCGCCGCCGCCAGTGAGAACCGGGGCCGGAG CACGGGGTGGGAGCGGAGCCCAGGCCGGGAGCCGGCGCCGCCGCCAGTGAGAACCGGGGCCGGAG A C TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:44891291..44891425 26863196 MeRIP-seq:(Medium) rs1312663118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773871,Human_RBP_ID_4557567,Human_RBP_ID_5117522,Human_RBP_ID_18421417,Human_RBP_ID_22533426 Human_Splice_Rec_2017829,Human_Splice_Rec_2017847,Human_Splice_Rec_2017865,Human_Splice_Rec_2017881 84804 RMVar_ID_84804 Human_SNP_ID_667041645 m1A Human chr19 + 44891301 44891301 44891301 CACGGGGTGGGAGCGGAGCCCAGGCCGGGAGCAGGCGCCGCCGCCAGTGAGAACCGGGGCCGGAG CACGGGGTGGGAGCGGAGCCCAGGCCGGGAGCTGGCGCCGCCGCCAGTGAGAACCGGGGCCGGAG A T TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:44891291..44891425 26863196 MeRIP-seq:(Medium) rs1312663118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773871,Human_RBP_ID_4557567,Human_RBP_ID_5117522,Human_RBP_ID_18421417,Human_RBP_ID_22533426 Human_Splice_Rec_2017829,Human_Splice_Rec_2017847,Human_Splice_Rec_2017865,Human_Splice_Rec_2017881 84805 RMVar_ID_84805 Human_SNP_ID_667041713 m1A Human chr19 + 44891460 44891460 44891460 TTGGCTGCCAGCTCGCCGCCCGCAGGGCCGCCACCGCCGCCTGCGCCGGCCCTCGTGGGGCTGCC TTGGCTGCCAGCTCGCCGCCCGCAGGGCCGCCGCCGCCGCCTGCGCCGGCCCTCGTGGGGCTGCC A G TOMM40 Ensembl:ENSG00000130204 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:44891226..44891525 26863410 MeRIP-seq:(Medium) rs1032590721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_908752,Human_RBP_ID_4557568,Human_RBP_ID_5116301,Human_RBP_ID_5374014,Human_RBP_ID_9329003 Human_Splice_Rec_2017828,Human_Splice_Rec_2017830,Human_Splice_Rec_2017848,Human_Splice_Rec_2017866,Human_Splice_Rec_2017882 84806 RMVar_ID_84806 Human_SNP_ID_667042474 m1A Human chr19 + 44893826 44893826 44893826 GGTGGGTGACATGGACAACAGTGGCAGTCTCAACGCTCAGGTCATTCACCAGCTGGGCCCCGGTC GGTGGGTGACATGGACAACAGTGGCAGTCTCAGCGCTCAGGTCATTCACCAGCTGGGCCCCGGTC A G TOMM40 Ensembl:ENSG00000130204 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:44893740..44893832;chr19:44893776..44893875 26863196 MeRIP-seq:(Medium) rs1431746988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1568190 Human_Splice_Rec_2017836,Human_Splice_Rec_2017837,Human_Splice_Rec_2017854,Human_Splice_Rec_2017855,Human_Splice_Rec_2017872,Human_Splice_Rec_2017873,Human_Splice_Rec_2017888,Human_Splice_Rec_2017889,Human_Splice_Rec_2017896,Human_Splice_Rec_2017897,Human_Splice_Rec_2017907 Human_miRNA_ID_2052792 RMVar_hsa_circ_12420,RMVar_hsa_circ_53813,RMVar_hsa_circ_98061,RMVar_hsa_circ_195250 84807 RMVar_ID_84807 Human_SNP_ID_667045324 m1A Human chr19 - 44903274 44903274 44903274 GTCCCTCCTTTCCAATGTCCCCCCCGACCCCCAAGGGGGGAGGGAAGGGAGGGGGGCTCAGGTCT GTCCCTCCTTTCCAATGTCCCCCCCGACCCCCCAGGGGGGAGGGAAGGGAGGGGGGCTCAGGTCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:44903226..44903275 26863196 MeRIP-seq:(Medium) rs878965943 Functional Loss SNV dbSNP153 33..33 33 - - - 84808 RMVar_ID_84808 Human_SNP_ID_667047445 m1A Human chr19 - 44909198 44909198 44909198 CAGGGGCGGCGCTGGTGCCCACGGCAGCCTGCACCTTCTCCACCAGCCCGGCCCACTGGCGCTGC CAGGGGCGGCGCTGGTGCCCACGGCAGCCTGCCCCTTCTCCACCAGCCCGGCCCACTGGCGCTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44908894..44909343 32194978 MeRIP-seq:(Medium) rs1418673754 Functional Loss SNV dbSNP153 33..33 33 - - - 84809 RMVar_ID_84809 Human_SNP_ID_667063394 m1A Human chr19 + 44962009 44962009 44962009 CAGCATCGGGAGGGACCCGCCAGCGGAGACCCAGCCTCAGAACCCACCGGCCCAGCCGGCACCCA CAGCATCGGGAGGGACCCGCCAGCGGAGACCCGGCCTCAGAACCCACCGGCCCAGCCGGCACCCA A G CLPTM1 Ensembl:ENSG00000104853 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:44961909..44962126;chr19:44961875..44962164;chr19:44961916..44962122;chr19:44955830..44974500 26863196 MeRIP-seq:(Medium) rs754110120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_911549,Human_RBP_ID_4536123,Human_RBP_ID_9381098,Human_RBP_ID_22447866,Human_RBP_ID_26336376,Human_RBP_ID_27815475 Human_Splice_Rec_2018066,Human_Splice_Rec_2018067,Human_Splice_Rec_2018080,Human_Splice_Rec_2018081,Human_Splice_Rec_2018105,Human_Splice_Rec_2018130,Human_Splice_Rec_2018131,Human_Splice_Rec_2018156,Human_Splice_Rec_2018157,Human_Splice_Rec_2018164,Human_Splice_Rec_2018165 RMVar_hsa_circ_59809,RMVar_hsa_circ_57961 84810 RMVar_ID_84810 Human_SNP_ID_667066694 m1A Human chr19 + 44973159 44973159 44973159 GGGCCGGCCCCTCAGGACCAGGCGGGCCCCGGAGGAGCTCCACGCGTCGCCAGCCGCAACCTGTT GGGCCGGCCCCTCAGGACCAGGCGGGCCCCGGCGGAGCTCCACGCGTCGCCAGCCGCAACCTGTT A C CLPTM1 Ensembl:ENSG00000104853 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:44973031..44973264;chr19:44973031..44973304 26863196 MeRIP-seq:(Medium) rs763110769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8427,Human_RBP_ID_239463,Human_RBP_ID_22447867,Human_RBP_ID_26468925 Human_Splice_Rec_2018068,Human_Splice_Rec_2018069,Human_Splice_Rec_2018082,Human_Splice_Rec_2018083,Human_Splice_Rec_2018106,Human_Splice_Rec_2018107,Human_Splice_Rec_2018132,Human_Splice_Rec_2018133,Human_Splice_Rec_2018158,Human_Splice_Rec_2018159,Human_Splice_Rec_2018166,Human_Splice_Rec_2018167 RMVar_hsa_circ_7756,RMVar_hsa_circ_59809,RMVar_hsa_circ_374212,RMVar_hsa_circ_57961,RMVar_hsa_circ_320125,RMVar_hsa_circ_195257,RMVar_hsa_circ_195258 84811 RMVar_ID_84811 Human_SNP_ID_667067092 m1A Human chr19 + 44974485 44974485 44974485 CATCTCAGAGCACGAGCACTTTACAGACTTCAACGCCACGTCGGCACTCTTCTGGGAACAGCACG CATCTCAGAGCACGAGCACTTTACAGACTTCACCGCCACGTCGGCACTCTTCTGGGAACAGCACG A C CLPTM1 Ensembl:ENSG00000104853 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:44974346..44974575 26863196 MeRIP-seq:(Medium) rs750258939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52980,Human_RBP_ID_1240067,Human_RBP_ID_1568206,Human_RBP_ID_1890015,Human_RBP_ID_3573707,Human_RBP_ID_4536132,Human_RBP_ID_8489973,Human_RBP_ID_13473007,Human_RBP_ID_17387416,Human_RBP_ID_21892291,Human_RBP_ID_22763038,Human_RBP_ID_24532949,Human_RBP_ID_26654440,Human_RBP_ID_26991453 Human_Splice_Rec_2018070,Human_Splice_Rec_2018084,Human_Splice_Rec_2018108,Human_Splice_Rec_2018134,Human_Splice_Rec_2018168 Human_miRNA_ID_2515980 RMVar_hsa_circ_7756,RMVar_hsa_circ_59809,RMVar_hsa_circ_374212,RMVar_hsa_circ_57961,RMVar_hsa_circ_320125,RMVar_hsa_circ_195259,RMVar_hsa_circ_42763,RMVar_hsa_circ_195257,RMVar_hsa_circ_195258,RMVar_hsa_circ_288833,RMVar_hsa_circ_195260 84812 RMVar_ID_84812 Human_SNP_ID_667067093 m1A Human chr19 + 44974485 44974485 44974485 CATCTCAGAGCACGAGCACTTTACAGACTTCAACGCCACGTCGGCACTCTTCTGGGAACAGCACG CATCTCAGAGCACGAGCACTTTACAGACTTCAGCGCCACGTCGGCACTCTTCTGGGAACAGCACG A G CLPTM1 Ensembl:ENSG00000104853 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:44974346..44974575 26863196 MeRIP-seq:(Medium) rs750258939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52980,Human_RBP_ID_1240067,Human_RBP_ID_1568206,Human_RBP_ID_1890015,Human_RBP_ID_3573707,Human_RBP_ID_4536132,Human_RBP_ID_8489973,Human_RBP_ID_13473007,Human_RBP_ID_17387416,Human_RBP_ID_21892291,Human_RBP_ID_22763038,Human_RBP_ID_24532949,Human_RBP_ID_26654440,Human_RBP_ID_26991453 Human_Splice_Rec_2018070,Human_Splice_Rec_2018084,Human_Splice_Rec_2018108,Human_Splice_Rec_2018134,Human_Splice_Rec_2018168 Human_miRNA_ID_2515980 RMVar_hsa_circ_7756,RMVar_hsa_circ_59809,RMVar_hsa_circ_374212,RMVar_hsa_circ_57961,RMVar_hsa_circ_320125,RMVar_hsa_circ_195259,RMVar_hsa_circ_42763,RMVar_hsa_circ_195257,RMVar_hsa_circ_195258,RMVar_hsa_circ_288833,RMVar_hsa_circ_195260 84813 RMVar_ID_84813 Human_SNP_ID_667071973 m1A Human chr19 + 44992317 44992317 44992317 GGCCCACCTTCCCTGGCGCATGCTCACCTACAAGGCCCTCAACACATTCATCGACGACCTGTTCG GGCCCACCTTCCCTGGCGCATGCTCACCTACACGGCCCTCAACACATTCATCGACGACCTGTTCG A C CLPTM1 Ensembl:ENSG00000104853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:44992268..44992341 26863196 MeRIP-seq:(Medium) rs778814856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139539,Human_RBP_ID_17269944,Human_RBP_ID_17384888,Human_RBP_ID_26815992,Human_RBP_ID_27469003 Human_Splice_Rec_2018102,Human_Splice_Rec_2018103,Human_Splice_Rec_2018126,Human_Splice_Rec_2018127,Human_Splice_Rec_2018152,Human_Splice_Rec_2018153,Human_Splice_Rec_2018192,Human_Splice_Rec_2018193,Human_Splice_Rec_2018199 84814 RMVar_ID_84814 Human_SNP_ID_667072192 m1A Human chr19 - 44992840 44992840 44992840 GGCTTTGGAGGGGCTTCCTGGGGCTCGCTGGCAGAGCTGGCCCCCTGGGTGGGCTTGGTGGGCAG GGCTTTGGAGGGGCTTCCTGGGGCTCGCTGGCGGAGCTGGCCCCCTGGGTGGGCTTGGTGGGCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:44992792..44992943 32194978 MeRIP-seq:(Medium) rs773267075 Functional Loss SNV dbSNP153 33..33 33 - - - 84815 RMVar_ID_84815 Human_SNP_ID_667072239 m1A Human chr19 + 44992939 44992939 44992939 GTCCTCACCTGCTCCGGCTCCTGGCGACCACTACCCCTGCGTCCCGGCCCCCTCGCCTCCCCTCC GTCCTCACCTGCTCCGGCTCCTGGCGACCACTGCCCCTGCGTCCCGGCCCCCTCGCCTCCCCTCC A G CLPTM1 Ensembl:ENSG00000104853 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44992892..44993042 32194978 MeRIP-seq:(Medium) rs1568391421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241222,Human_RBP_ID_523439,Human_RBP_ID_8256214,Human_RBP_ID_18945640,Human_RBP_ID_22592086,Human_RBP_ID_22764170,Human_RBP_ID_26991483 Human_miRNA_ID_291983 84816 RMVar_ID_84816 Human_SNP_ID_111268145 m1A Human chr2 + 210002680 210002680 210002680 TGGGAGCCAGCGGTATGGCGTCGGGCTGCAAGATTGGCCCGTCCATCCTCAACAGCGACCTGGCC TGGGAGCCAGCGGTATGGCGTCGGGCTGCAAGGTTGGCCCGTCCATCCTCAACAGCGACCTGGCC A G RPE Ensembl:ENSG00000197713 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:210002647..210002733 26863410 MeRIP-seq:(Medium) rs750802630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244009,Human_RBP_ID_18422010,Human_RBP_ID_23119504 Human_Splice_Rec_352701,Human_Splice_Rec_352709 84817 RMVar_ID_84817 Human_SNP_ID_111268146 m1A Human chr2 + 210002680 210002680 210002680 TGGGAGCCAGCGGTATGGCGTCGGGCTGCAAGATTGGCCCGTCCATCCTCAACAGCGACCTGGCC TGGGAGCCAGCGGTATGGCGTCGGGCTGCAAGTTTGGCCCGTCCATCCTCAACAGCGACCTGGCC A T RPE Ensembl:ENSG00000197713 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:210002647..210002733 26863410 MeRIP-seq:(Medium) rs750802630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244009,Human_RBP_ID_18422010,Human_RBP_ID_23119504 Human_Splice_Rec_352701,Human_Splice_Rec_352709 84818 RMVar_ID_84818 Human_SNP_ID_111268175 m1A Human chr2 - 210002728 210002723 210002728 ATAATCGGCCCCAGAGTCTAGCATCCGGAGGCACTCGGCCCCTAAATTGGCCAGGTCGCTGTTGA ATAATCGGCCCCAGAGTCTAGCATCCGGAGGC_____GCCCCTAAATTGGCCAGGTCGCTGTTGA CCGAGT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:210002663..210003467 32194978 MeRIP-seq:(Medium) rs1471154086 Functional Loss DEL dbSNP153 33..37 33 - - - 84819 RMVar_ID_84819 Human_SNP_ID_111271950 m1A Human chr2 + 210017519 210017519 210017519 GACCCAGTTCCCATCTTTGGATATAGAGGTCGATGGTGGAGTAGGTCCTGACACTGTCCATAAAT GACCCAGTTCCCATCTTTGGATATAGAGGTCGTTGGTGGAGTAGGTCCTGACACTGTCCATAAAT A T RPE Ensembl:ENSG00000197713 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:210016070..210017540 32194978 MeRIP-seq:(Medium) rs769009455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923154,Human_RBP_ID_1909149,Human_RBP_ID_8510763,Human_RBP_ID_13758490,Human_RBP_ID_17965010,Human_RBP_ID_19098623,Human_RBP_ID_23851237 Human_Splice_Rec_352584,Human_Splice_Rec_352585,Human_Splice_Rec_352594,Human_Splice_Rec_352595,Human_Splice_Rec_352604,Human_Splice_Rec_352605,Human_Splice_Rec_352616,Human_Splice_Rec_352617,Human_Splice_Rec_352636,Human_Splice_Rec_352637,Human_Splice_Rec_352648,Human_Splice_Rec_352649,Human_Splice_Rec_352658,Human_Splice_Rec_352659,Human_Splice_Rec_352670,Human_Splice_Rec_352676,Human_Splice_Rec_352677,Human_Splice_Rec_352688,Human_Splice_Rec_352689,Human_Splice_Rec_352698,Human_Splice_Rec_352699,Human_Splice_Rec_352716,Human_Splice_Rec_352717,Human_Splice_Rec_352726,Human_Splice_Rec_352727 RMVar_hsa_circ_206528,RMVar_hsa_circ_359665,RMVar_hsa_circ_206530,RMVar_hsa_circ_342865,RMVar_hsa_circ_377913,RMVar_hsa_circ_206529 84820 RMVar_ID_84820 Human_SNP_ID_111384013 m1A Human chr2 - 210476677 210476677 210476677 GGCCGAGAAGGGCTTCAGGACGCGGGAGGCGCACTTGCTTCAAGTCGCGGGCGTGGGAACGGGGT GGCCGAGAAGGGCTTCAGGACGCGGGAGGCGCGCTTGCTTCAAGTCGCGGGCGTGGGAACGGGGT T C LANCL1 Ensembl:ENSG00000115365 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:210476584..210476725;chr2:210476474..210476725;chr2:210476522..210476725 26863196 MeRIP-seq:(Medium) rs765290197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623827,Human_RBP_ID_6882435,Human_RBP_ID_22505027,Human_RBP_ID_22670380 Human_Splice_Rec_353001,Human_Splice_Rec_353019,Human_Splice_Rec_353071 84821 RMVar_ID_84821 Human_SNP_ID_111396875 m1A Human chr2 - 210525729 210525729 210525729 TTAAGCAAATTTCTACTTGTTTCCTAAGGCTCAGCCCAGCTATCCTCTCCTGCAAGCCATCACTG TTAAGCAAATTTCTACTTGTTTCCTAAGGCTCGGCCCAGCTATCCTCTCCTGCAAGCCATCACTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:210525722..210526011 26863196 MeRIP-seq:(Medium) rs1034680583 Functional Loss SNV dbSNP153 33..33 33 - - - 84822 RMVar_ID_84822 Human_SNP_ID_111411104 m1A Human chr2 - 210588128 210588128 210588128 ACAAATTACTTACCTTTACTAGCAGGCGGATTACATTGTTTTTAATCCCACAGTCTACAGCTACC ACAAATTACTTACCTTTACTAGCAGGCGGATTGCATTGTTTTTAATCCCACAGTCTACAGCTACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210588007..210588200 26863196 MeRIP-seq:(Medium) rs1308610893 Functional Loss SNV dbSNP153 33..33 33 - - - 84823 RMVar_ID_84823 Human_SNP_ID_111411739 m1A Human chr2 + 210590766 210590766 210590766 GTTCATTCAGAAGCAACATTTTTTGGAACTGTACTAATTGGTTAATAAAAATTCTCCCTGATTTA GTTCATTCAGAAGCAACATTTTTTGGAACTGTGCTAATTGGTTAATAAAAATTCTCCCTGATTTA A G CPS1 Ensembl:ENSG00000021826 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210590762..210590889 26863196 MeRIP-seq:(Medium) rs368879550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_206565,RMVar_hsa_circ_120897,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_348714,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_71417,RMVar_hsa_circ_31823,RMVar_hsa_circ_21428,RMVar_hsa_circ_56740,RMVar_hsa_circ_54386,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_72435,RMVar_hsa_circ_63497,RMVar_hsa_circ_68775,RMVar_hsa_circ_59196,RMVar_hsa_circ_69514,RMVar_hsa_circ_70421,RMVar_hsa_circ_100412,RMVar_hsa_circ_369618,RMVar_hsa_circ_70074,RMVar_hsa_circ_60244,RMVar_hsa_circ_55652,RMVar_hsa_circ_73167,RMVar_hsa_circ_206566,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_60939,RMVar_hsa_circ_361168,RMVar_hsa_circ_69154,RMVar_hsa_circ_69776 84824 RMVar_ID_84824 Human_SNP_ID_111412336 m1A Human chr2 + 210592928 210592928 210592928 CAAACCCTTCTTCGCTGTGCAGTTCCACCCAGAGGTCACCCCGGGGCCAATAGACACTGAGGTAC CAAACCCTTCTTCGCTGTGCAGTTCCACCCAGTGGTCACCCCGGGGCCAATAGACACTGAGGTAC A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210592846..210592954 26863196 MeRIP-seq:(Medium) rs756428203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55907,Human_RBP_ID_304446,Human_RBP_ID_8511007 Human_Splice_Rec_353102,Human_Splice_Rec_353103,Human_Splice_Rec_353180,Human_Splice_Rec_353181,Human_Splice_Rec_353256,Human_Splice_Rec_353257,Human_Splice_Rec_353332,Human_Splice_Rec_353333,Human_Splice_Rec_353406,Human_Splice_Rec_353407,Human_Splice_Rec_353480,Human_Splice_Rec_353481 Human_miRNA_ID_2423322,Human_miRNA_ID_2432982 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_348714,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_31823,RMVar_hsa_circ_21428,RMVar_hsa_circ_22952,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_72435,RMVar_hsa_circ_68775,RMVar_hsa_circ_59196,RMVar_hsa_circ_69514,RMVar_hsa_circ_70421,RMVar_hsa_circ_100412,RMVar_hsa_circ_70074,RMVar_hsa_circ_60244,RMVar_hsa_circ_55652,RMVar_hsa_circ_73167,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_60939,RMVar_hsa_circ_361168,RMVar_hsa_circ_69154,RMVar_hsa_circ_69776,RMVar_hsa_circ_80365,RMVar_hsa_circ_58119,RMVar_hsa_circ_70790,RMVar_hsa_circ_74265,RMVar_hsa_circ_84316,RMVar_hsa_circ_206568,RMVar_hsa_circ_206569,RMVar_hsa_circ_74078,RMVar_hsa_circ_366254 84825 RMVar_ID_84825 Human_SNP_ID_111413892 m1A Human chr2 + 210599548 210599548 210599548 GATGGGTTAATTCTGGGCATGGGTGGCCAGACAGCTCTGAACTGTGGTGAGTTCTTATAAGCTTA GATGGGTTAATTCTGGGCATGGGTGGCCAGACGGCTCTGAACTGTGGTGAGTTCTTATAAGCTTA A G CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210599411..210599608 26863196 MeRIP-seq:(Medium) rs369446664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921666 Human_Splice_Rec_353109,Human_Splice_Rec_353187,Human_Splice_Rec_353263,Human_Splice_Rec_353339,Human_Splice_Rec_353413,Human_Splice_Rec_353495,Human_Splice_Rec_353549,Human_Splice_Rec_353597 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_21428,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_72435,RMVar_hsa_circ_69514,RMVar_hsa_circ_100412,RMVar_hsa_circ_70074,RMVar_hsa_circ_55652,RMVar_hsa_circ_73167,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_60939,RMVar_hsa_circ_69154,RMVar_hsa_circ_69776,RMVar_hsa_circ_80365,RMVar_hsa_circ_58119,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_74078,RMVar_hsa_circ_73146,RMVar_hsa_circ_24212,RMVar_hsa_circ_58944,RMVar_hsa_circ_86182,RMVar_hsa_circ_102148,RMVar_hsa_circ_75386,RMVar_hsa_circ_206570,RMVar_hsa_circ_206571 84826 RMVar_ID_84826 Human_SNP_ID_111415381 m1A Human chr2 - 210605765 210605761 210605765 ACAGTTTCCAGTGTCTTTGTATCAACTTATTTATTTCTATTTTATTTCTTAAATTCCATCTCCAC ACAGTTTCCAGTGTCTTTGTATCAACTTATTT____CTATTTTATTTCTTAAATTCCATCTCCAC GAAAT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:210605762..210605919 26863196 MeRIP-seq:(Medium) rs1288626899 Functional Loss DEL dbSNP153 33..36 33 - - - 84827 RMVar_ID_84827 Human_SNP_ID_111422026 m1A Human chr2 + 210634512 210634512 210634512 CTCTCTTTTTCTTGAAAGTAAAAGTAACCACAAACTTTGGTGTTTCCAAGGCTCTCTGAAGCTCT CTCTCTTTTTCTTGAAAGTAAAAGTAACCACAGACTTTGGTGTTTCCAAGGCTCTCTGAAGCTCT A G CPS1 Ensembl:ENSG00000021826 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:210634509..210634650 26863196 MeRIP-seq:(Medium) rs548440237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2620639 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_72954,RMVar_hsa_circ_100412,RMVar_hsa_circ_206567,RMVar_hsa_circ_80365,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_86182,RMVar_hsa_circ_206571,RMVar_hsa_circ_81683,RMVar_hsa_circ_206572,RMVar_hsa_circ_75142,RMVar_hsa_circ_352319,RMVar_hsa_circ_206575 84828 RMVar_ID_84828 Human_SNP_ID_111422751 m1A Human chr2 + 210637803 210637803 210637803 ATGCCTTGGGCTCACTGAGGCCCAGACAAGGGAGCTGAGGTTAAAGAAAAACATCCACCCTTGGG ATGCCTTGGGCTCACTGAGGCCCAGACAAGGGGGCTGAGGTTAAAGAAAAACATCCACCCTTGGG A G CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210637752..210637886 26863196 MeRIP-seq:(Medium) rs771770670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55962 Human_Splice_Rec_353125,Human_Splice_Rec_353203,Human_Splice_Rec_353279,Human_Splice_Rec_353355,Human_Splice_Rec_353429,Human_Splice_Rec_353511,Human_Splice_Rec_353565,Human_Splice_Rec_353613,Human_Splice_Rec_353651 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_72954,RMVar_hsa_circ_100412,RMVar_hsa_circ_206567,RMVar_hsa_circ_80365,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_86182,RMVar_hsa_circ_206571,RMVar_hsa_circ_81683,RMVar_hsa_circ_206572,RMVar_hsa_circ_75142,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_365144,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_367818,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_66380,RMVar_hsa_circ_123166,RMVar_hsa_circ_65057,RMVar_hsa_circ_206576 84829 RMVar_ID_84829 Human_SNP_ID_111422752 m1A Human chr2 + 210637803 210637803 210637803 ATGCCTTGGGCTCACTGAGGCCCAGACAAGGGAGCTGAGGTTAAAGAAAAACATCCACCCTTGGG ATGCCTTGGGCTCACTGAGGCCCAGACAAGGGTGCTGAGGTTAAAGAAAAACATCCACCCTTGGG A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210637752..210637886 26863196 MeRIP-seq:(Medium) rs771770670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55962 Human_Splice_Rec_353125,Human_Splice_Rec_353203,Human_Splice_Rec_353279,Human_Splice_Rec_353355,Human_Splice_Rec_353429,Human_Splice_Rec_353511,Human_Splice_Rec_353565,Human_Splice_Rec_353613,Human_Splice_Rec_353651 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_72954,RMVar_hsa_circ_100412,RMVar_hsa_circ_206567,RMVar_hsa_circ_80365,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_86182,RMVar_hsa_circ_206571,RMVar_hsa_circ_81683,RMVar_hsa_circ_206572,RMVar_hsa_circ_75142,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_365144,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_367818,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_66380,RMVar_hsa_circ_123166,RMVar_hsa_circ_65057,RMVar_hsa_circ_206576 84830 RMVar_ID_84830 Human_SNP_ID_111426250 m1A Human chr2 - 210653101 210653101 210653101 CAAATCTCAACTCACCCTTCAAGGCCTAGGTCATATGCTATCTCCTCCCTGAATCCTTCTCTGAA CAAATCTCAACTCACCCTTCAAGGCCTAGGTCGTATGCTATCTCCTCCCTGAATCCTTCTCTGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210653099..210653174 26863196 MeRIP-seq:(Medium) rs542275296 Functional Loss SNV dbSNP153 33..33 33 - - - 84831 RMVar_ID_84831 Human_SNP_ID_111426495 m1A Human chr2 + 210654080 210654080 210654080 ATTTGTTGAAGGGGCCCGAGAAGTAGAAATGGACGCTGTTGGCAAAGATGGAAGGGTAAGTGCTT ATTTGTTGAAGGGGCCCGAGAAGTAGAAATGGCCGCTGTTGGCAAAGATGGAAGGGTAAGTGCTT A C CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210653990..210654148 26863196 MeRIP-seq:(Medium) rs1437722789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55997,Human_RBP_ID_921673 Human_Splice_Rec_353138,Human_Splice_Rec_353139,Human_Splice_Rec_353216,Human_Splice_Rec_353217,Human_Splice_Rec_353292,Human_Splice_Rec_353293,Human_Splice_Rec_353368,Human_Splice_Rec_353369,Human_Splice_Rec_353442,Human_Splice_Rec_353443,Human_Splice_Rec_353524,Human_Splice_Rec_353525,Human_Splice_Rec_353578,Human_Splice_Rec_353579,Human_Splice_Rec_353628,Human_Splice_Rec_353629 RMVar_hsa_circ_297846,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_6014,RMVar_hsa_circ_56320,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_66380,RMVar_hsa_circ_103202,RMVar_hsa_circ_360360,RMVar_hsa_circ_368273,RMVar_hsa_circ_63118,RMVar_hsa_circ_355151,RMVar_hsa_circ_353791,RMVar_hsa_circ_55792,RMVar_hsa_circ_56784,RMVar_hsa_circ_69366,RMVar_hsa_circ_206577,RMVar_hsa_circ_55863,RMVar_hsa_circ_6227,RMVar_hsa_circ_56999 84832 RMVar_ID_84832 Human_SNP_ID_111427010 m1A Human chr2 + 210656528 210656528 210656528 TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTATCTCTCATGCCATCTCTGAACATGTTGAAGAT TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTGTCTCTCATGCCATCTCTGAACATGTTGAAGAT A G CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210656526..210656654 26863196 MeRIP-seq:(Medium) rs779559626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56002,Human_RBP_ID_2620884,Human_RBP_ID_8511123 Human_Splice_Rec_353140,Human_Splice_Rec_353218,Human_Splice_Rec_353294,Human_Splice_Rec_353370,Human_Splice_Rec_353444,Human_Splice_Rec_353526,Human_Splice_Rec_353580,Human_Splice_Rec_353630 RMVar_hsa_circ_297846,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_6014,RMVar_hsa_circ_56320,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_103202,RMVar_hsa_circ_360360,RMVar_hsa_circ_368273,RMVar_hsa_circ_355151,RMVar_hsa_circ_353791,RMVar_hsa_circ_55792,RMVar_hsa_circ_56784,RMVar_hsa_circ_69366,RMVar_hsa_circ_206577,RMVar_hsa_circ_55863,RMVar_hsa_circ_6227,RMVar_hsa_circ_56999,RMVar_hsa_circ_57477 84833 RMVar_ID_84833 Human_SNP_ID_111427011 m1A Human chr2 + 210656528 210656528 210656528 TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTATCTCTCATGCCATCTCTGAACATGTTGAAGAT TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTTTCTCTCATGCCATCTCTGAACATGTTGAAGAT A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210656526..210656654 26863196 MeRIP-seq:(Medium) rs779559626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56002,Human_RBP_ID_2620884,Human_RBP_ID_8511123 Human_Splice_Rec_353140,Human_Splice_Rec_353218,Human_Splice_Rec_353294,Human_Splice_Rec_353370,Human_Splice_Rec_353444,Human_Splice_Rec_353526,Human_Splice_Rec_353580,Human_Splice_Rec_353630 RMVar_hsa_circ_297846,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_6014,RMVar_hsa_circ_56320,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_103202,RMVar_hsa_circ_360360,RMVar_hsa_circ_368273,RMVar_hsa_circ_355151,RMVar_hsa_circ_353791,RMVar_hsa_circ_55792,RMVar_hsa_circ_56784,RMVar_hsa_circ_69366,RMVar_hsa_circ_206577,RMVar_hsa_circ_55863,RMVar_hsa_circ_6227,RMVar_hsa_circ_56999,RMVar_hsa_circ_57477 84834 RMVar_ID_84834 Human_SNP_ID_111431762 m1A Human chr2 - 210674955 210674955 210674955 AAACAACTTAAAACTAATGAACATACCTTGAAACCTTCATTGTGTAATTGTTCAGCCACACCAAG AAACAACTTAAAACTAATGAACATACCTTGAAGCCTTCATTGTGTAATTGTTCAGCCACACCAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210674863..210675006 26863196 MeRIP-seq:(Medium) rs1200099747 Functional Loss SNV dbSNP153 33..33 33 - - - 84835 RMVar_ID_84835 Human_SNP_ID_111434288 m1A Human chr2 - 210685183 210685183 210685183 TCCCTCCTTCTCTTTCTTCCTCCTGTATCATTATAATGGCTTCCTAACTAGTCTCTCTGCCTCCA TCCCTCCTTCTCTTTCTTCCTCCTGTATCATTGTAATGGCTTCCTAACTAGTCTCTCTGCCTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:210685132..210685382 26863196 MeRIP-seq:(Medium) rs1291728424 Functional Loss SNV dbSNP153 33..33 33 - - - 84836 RMVar_ID_84836 Human_SNP_ID_111434573 m1A Human chr2 + 210686567 210686567 210686567 ACAGAGGTGAAGGGAGGAAGTGTAGAGAAGCAATGAGTCTGCAGCAGCAGGGGAAAGAGTAAACA ACAGAGGTGAAGGGAGGAAGTGTAGAGAAGCAGTGAGTCTGCAGCAGCAGGGGAAAGAGTAAACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:210686516..210686655 26863196 MeRIP-seq:(Medium) rs1314211510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2621426 84837 RMVar_ID_84837 Human_SNP_ID_111824269 m1A Human chr2 + 212171653 212171653 212171653 CTTCCCCCATGCTGTTCTTATAATAGTGAGCTAGTTCTCATGAGATATGATGGTTTTATAAGGGT CTTCCCCCATGCTGTTCTTATAATAGTGAGCTGGTTCTCATGAGATATGATGGTTTTATAAGGGT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:212171638..212171751 26863196 MeRIP-seq:(Medium) rs1226547217 Functional Loss SNV dbSNP153 33..33 33 - - - 84838 RMVar_ID_84838 Human_SNP_ID_112065258 m1A Human chr2 + 213151954 213151954 213151954 GGCAATCGATTACAGGACAAGTGCTGCCCCGGAGGCTCCGCGACGCGCGCACTCCCTCGCGCCCA GGCAATCGATTACAGGACAAGTGCTGCCCCGGTGGCTCCGCGACGCGCGCACTCCCTCGCGCCCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:213151945..213152106 26863196 MeRIP-seq:(Medium) rs1221125471 Functional Loss SNV dbSNP153 33..33 33 - - - 84839 RMVar_ID_84839 Human_SNP_ID_112097551 m1A Human chr2 + 213284482 213284482 213284482 GGCCTGCTGGGGGTGGGGGCCCGAAGCGCCAGAGATGGCTGCTCAGCGAGGGATGCCCAGCTCCG GGCCTGCTGGGGGTGGGGGCCCGAAGCGCCAGCGATGGCTGCTCAGCGAGGGATGCCCAGCTCCG A C SPAG16 Ensembl:ENSG00000144451 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:213284413..213284660 26863196 MeRIP-seq:(Medium) rs1236147543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830752,Human_RBP_ID_5380049,Human_RBP_ID_9353823,Human_RBP_ID_9387898,Human_RBP_ID_18422012,Human_RBP_ID_22997511 RMVar_hsa_circ_117031,RMVar_hsa_circ_206634 84840 RMVar_ID_84840 Human_SNP_ID_112474749 m1A Human chr2 - 214798454 214798454 214798454 AGCTTGCCACGAAATAGAATTCAGTACACTTGATGGGGAAAAGGAGGTTAGGTTTGCTAGGTCAA AGCTTGCCACGAAATAGAATTCAGTACACTTGGTGGGGAAAAGGAGGTTAGGTTTGCTAGGTCAA T C BARD1 Ensembl:ENSG00000138376 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:214798448..214798521 26863196 MeRIP-seq:(Medium) rs1398064191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13764682 84841 RMVar_ID_84841 Human_SNP_ID_112487300 m1A Human chr2 + 214847285 214847285 214847285 CCTGCGCAGGGCCAAGTTCAAGCTTCCTGGCCACCAGAAGATCCACATCTCAAAGAAGTGGGGCT CCTGCGCAGGGCCAAGTTCAAGCTTCCTGGCCGCCAGAAGATCCACATCTCAAAGAAGTGGGGCT A G SNHG31,RPL10P6 Ensembl:ENSG00000229267,Ensembl:ENSG00000230076 lincRNA,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs928716168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393733 RMVar_hsa_circ_206682 84842 RMVar_ID_84842 Human_SNP_ID_112487349 m1A Human chr2 + 214847503 214847502 214847503 TTAATACTCACCAATAAATTCTACTTCCTGTCAAAAAAATGTCACTAATGTACCCTAAATTTTCT TTAATACTCACCAATAAATTCTACTTCCTGTC_AAAAAATGTCACTAATGTACCCTAAATTTTCT CA C SNHG31 Ensembl:ENSG00000229267 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1448274769 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_543850,Human_RBP_ID_1240885,Human_RBP_ID_3615403,Human_RBP_ID_26488197 RMVar_hsa_circ_206682 84843 RMVar_ID_84843 Human_SNP_ID_112487350 m1A Human chr2 + 214847503 214847503 214847503 TTAATACTCACCAATAAATTCTACTTCCTGTCAAAAAAATGTCACTAATGTACCCTAAATTTTCT TTAATACTCACCAATAAATTCTACTTCCTGTCCAAAAAATGTCACTAATGTACCCTAAATTTTCT A C SNHG31 Ensembl:ENSG00000229267 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879029686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_543850,Human_RBP_ID_1240885,Human_RBP_ID_3615403,Human_RBP_ID_26488197 RMVar_hsa_circ_206682 84844 RMVar_ID_84844 Human_SNP_ID_112487351 m1A Human chr2 + 214847503 214847503 214847503 TTAATACTCACCAATAAATTCTACTTCCTGTCAAAAAAATGTCACTAATGTACCCTAAATTTTCT TTAATACTCACCAATAAATTCTACTTCCTGTCGAAAAAATGTCACTAATGTACCCTAAATTTTCT A G SNHG31 Ensembl:ENSG00000229267 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879029686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_543850,Human_RBP_ID_1240885,Human_RBP_ID_3615403,Human_RBP_ID_26488197 RMVar_hsa_circ_206682 84845 RMVar_ID_84845 Human_SNP_ID_112602852 m1A Human chr2 - 215312441 215312441 215312441 ATGATTCGCAGCACATTGCACTGTGTTCTGCAAGGCCTTGGGAGGGTCTGGGGGAGGAGATTCTC ATGATTCGCAGCACATTGCACTGTGTTCTGCATGGCCTTGGGAGGGTCTGGGGGAGGAGATTCTC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:215312432..215312575 26863410 MeRIP-seq:(Medium) rs983166180 Functional Loss SNV dbSNP153 33..33 33 - - - 84846 RMVar_ID_84846 Human_SNP_ID_112617332 m1A Human chr2 - 215364987 215364987 215364987 CTTATGCGTGCATCTGTCTTGTGTCTATATGCAGATGAGGCAACGTGTTATGATGATGGGAAGAC CTTATGCGTGCATCTGTCTTGTGTCTATATGCTGATGAGGCAACGTGTTATGATGATGGGAAGAC T A FN1 Ensembl:ENSG00000115414 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:215364942..215365025 26863196 MeRIP-seq:(Medium) rs111376415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102121,RMVar_hsa_circ_64309,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_364530,RMVar_hsa_circ_206714 84847 RMVar_ID_84847 Human_SNP_ID_112619352 m1A Human chr2 - 215372017 215372017 215372017 CACGGTCCGGGACTCAATCCAAATGCCTCTACAGGACAAGAAGCTCTCTCTCAGACAACCATCTC CACGGTCCGGGACTCAATCCAAATGCCTCTACGGGACAAGAAGCTCTCTCTCAGACAACCATCTC T C FN1 Ensembl:ENSG00000115414 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:215372001..215372025 32194978 MeRIP-seq:(Medium) rs753952665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142808 Human_miRNA_ID_2254160 RMVar_hsa_circ_21977,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_107531,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_67479,RMVar_hsa_circ_206715,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_71814,RMVar_hsa_circ_358568,RMVar_hsa_circ_63624,RMVar_hsa_circ_66833,RMVar_hsa_circ_61636,RMVar_hsa_circ_55828,RMVar_hsa_circ_325049,RMVar_hsa_circ_334043,RMVar_hsa_circ_355425,RMVar_hsa_circ_115444,RMVar_hsa_circ_265376,RMVar_hsa_circ_106084,RMVar_hsa_circ_206719,RMVar_hsa_circ_206720 84848 RMVar_ID_84848 Human_SNP_ID_112619408 m1A Human chr2 - 215372145 215372145 215372145 GGCGGACCACACCGCCCACAACGGCCACCCCCATAAGGCATAGGCCAAGACCATACCCGCCGAAT GGCGGACCACACCGCCCACAACGGCCACCCCCGTAAGGCATAGGCCAAGACCATACCCGCCGAAT T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215371976..215372400 32194978 MeRIP-seq:(Medium) rs1286651800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142808,Human_RBP_ID_775151,Human_RBP_ID_921705,Human_RBP_ID_8852186,Human_RBP_ID_17279235,Human_RBP_ID_17392865,Human_RBP_ID_17510212,Human_RBP_ID_22450666,Human_RBP_ID_22765236 Human_Splice_Rec_355101,Human_Splice_Rec_355283,Human_Splice_Rec_355373,Human_Splice_Rec_355583,Human_Splice_Rec_355673,Human_Splice_Rec_355761,Human_Splice_Rec_356003 Human_miRNA_ID_2869343,Human_miRNA_ID_2869344 RMVar_hsa_circ_21977,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_107531,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_67479,RMVar_hsa_circ_206715,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_71814,RMVar_hsa_circ_358568,RMVar_hsa_circ_63624,RMVar_hsa_circ_66833,RMVar_hsa_circ_61636,RMVar_hsa_circ_79478,RMVar_hsa_circ_55828,RMVar_hsa_circ_325049,RMVar_hsa_circ_334043,RMVar_hsa_circ_355425,RMVar_hsa_circ_115444,RMVar_hsa_circ_265376,RMVar_hsa_circ_106084,RMVar_hsa_circ_122684,RMVar_hsa_circ_206719,RMVar_hsa_circ_206720,RMVar_hsa_circ_88845,RMVar_hsa_circ_206721,RMVar_hsa_circ_206722,RMVar_hsa_circ_206723 84849 RMVar_ID_84849 Human_SNP_ID_112619748 m1A Human chr2 - 215373393 215373393 215373393 TATTCTCCCTTCAGGCCTGGAACCGGGAACCGAATATACAATTTATGTCATTGCCCTGAAGAATA TATTCTCCCTTCAGGCCTGGAACCGGGAACCGGATATACAATTTATGTCATTGCCCTGAAGAATA T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:215373268..215373468 26863196 MeRIP-seq:(Medium) rs1369574351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775153,Human_RBP_ID_829285,Human_RBP_ID_921708,Human_RBP_ID_5239700,Human_RBP_ID_17279251,Human_RBP_ID_17509816,Human_RBP_ID_17965685,Human_RBP_ID_22766131 Human_Splice_Rec_355098,Human_Splice_Rec_355099,Human_Splice_Rec_355190,Human_Splice_Rec_355191,Human_Splice_Rec_355280,Human_Splice_Rec_355281,Human_Splice_Rec_355370,Human_Splice_Rec_355371,Human_Splice_Rec_355458,Human_Splice_Rec_355459,Human_Splice_Rec_355546,Human_Splice_Rec_355547,Human_Splice_Rec_355580,Human_Splice_Rec_355581,Human_Splice_Rec_355670,Human_Splice_Rec_355671,Human_Splice_Rec_355758,Human_Splice_Rec_355759,Human_Splice_Rec_355848,Human_Splice_Rec_355849,Human_Splice_Rec_355936,Human_Splice_Rec_355937,Human_Splice_Rec_355976,Human_Splice_Rec_355977,Human_Splice_Rec_356012,Human_Splice_Rec_356013,Human_Splice_Rec_356018,Human_Splice_Rec_356019 RMVar_hsa_circ_21977,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_107531,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_67479,RMVar_hsa_circ_206715,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_71814,RMVar_hsa_circ_358568,RMVar_hsa_circ_63624,RMVar_hsa_circ_61636,RMVar_hsa_circ_79478,RMVar_hsa_circ_55828,RMVar_hsa_circ_325049,RMVar_hsa_circ_355425,RMVar_hsa_circ_115444,RMVar_hsa_circ_265376,RMVar_hsa_circ_106084,RMVar_hsa_circ_122684,RMVar_hsa_circ_206719,RMVar_hsa_circ_206720,RMVar_hsa_circ_88845,RMVar_hsa_circ_103151,RMVar_hsa_circ_354220,RMVar_hsa_circ_206721,RMVar_hsa_circ_206722,RMVar_hsa_circ_206723,RMVar_hsa_circ_355578,RMVar_hsa_circ_364716,RMVar_hsa_circ_301923,RMVar_hsa_circ_352011,RMVar_hsa_circ_119789,RMVar_hsa_circ_53921,RMVar_hsa_circ_81432,RMVar_hsa_circ_206725,RMVar_hsa_circ_206727,RMVar_hsa_circ_31332,RMVar_hsa_circ_206726,RMVar_hsa_circ_206724 84850 RMVar_ID_84850 Human_SNP_ID_112623838 m1A Human chr2 - 215388301 215388301 215388301 AGTTTTAAAATAAGCCCCATTTGCCCCTACAGATCTCCTGCCTGGTACAGAATATGTAGTGAGTG AGTTTTAAAATAAGCCCCATTTGCCCCTACAGGTCTCCTGCCTGGTACAGAATATGTAGTGAGTG T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215388260..215391840 32194978 MeRIP-seq:(Medium) rs781729898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921726,Human_RBP_ID_5239708,Human_RBP_ID_5528787,Human_RBP_ID_22451795,Human_RBP_ID_22670391 Human_Splice_Rec_355076,Human_Splice_Rec_355077,Human_Splice_Rec_355166,Human_Splice_Rec_355167,Human_Splice_Rec_355256,Human_Splice_Rec_355257,Human_Splice_Rec_355346,Human_Splice_Rec_355347,Human_Splice_Rec_355436,Human_Splice_Rec_355437,Human_Splice_Rec_355522,Human_Splice_Rec_355523,Human_Splice_Rec_355562,Human_Splice_Rec_355563,Human_Splice_Rec_355646,Human_Splice_Rec_355647,Human_Splice_Rec_355736,Human_Splice_Rec_355737,Human_Splice_Rec_355826,Human_Splice_Rec_355827,Human_Splice_Rec_355914,Human_Splice_Rec_355915,Human_Splice_Rec_355954,Human_Splice_Rec_355955 RMVar_hsa_circ_23898,RMVar_hsa_circ_3650,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_107531,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_67479,RMVar_hsa_circ_206715,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_63624,RMVar_hsa_circ_79478,RMVar_hsa_circ_265376,RMVar_hsa_circ_106084,RMVar_hsa_circ_122684,RMVar_hsa_circ_206720,RMVar_hsa_circ_88845,RMVar_hsa_circ_103151,RMVar_hsa_circ_206721,RMVar_hsa_circ_206722,RMVar_hsa_circ_206723,RMVar_hsa_circ_301923,RMVar_hsa_circ_53921,RMVar_hsa_circ_81432,RMVar_hsa_circ_206725,RMVar_hsa_circ_206727,RMVar_hsa_circ_206726,RMVar_hsa_circ_380,RMVar_hsa_circ_120836,RMVar_hsa_circ_93135,RMVar_hsa_circ_121202,RMVar_hsa_circ_99058,RMVar_hsa_circ_206728,RMVar_hsa_circ_206730,RMVar_hsa_circ_206729,RMVar_hsa_circ_123745,RMVar_hsa_circ_82975,RMVar_hsa_circ_113512,RMVar_hsa_circ_23850,RMVar_hsa_circ_206733,RMVar_hsa_circ_206734,RMVar_hsa_circ_206735,RMVar_hsa_circ_206732,RMVar_hsa_circ_37635,RMVar_hsa_circ_112126,RMVar_hsa_circ_53090,RMVar_hsa_circ_56306,RMVar_hsa_circ_72390,RMVar_hsa_circ_206738,RMVar_hsa_circ_375352,RMVar_hsa_circ_45854,RMVar_hsa_circ_51496,RMVar_hsa_circ_30025,RMVar_hsa_circ_206740,RMVar_hsa_circ_110836,RMVar_hsa_circ_101080,RMVar_hsa_circ_74032,RMVar_hsa_circ_268941,RMVar_hsa_circ_206741,RMVar_hsa_circ_269134,RMVar_hsa_circ_266791,RMVar_hsa_circ_60027,RMVar_hsa_circ_206742,RMVar_hsa_circ_100587,RMVar_hsa_circ_116298,RMVar_hsa_circ_361649,RMVar_hsa_circ_206744,RMVar_hsa_circ_1348,RMVar_hsa_circ_64680,RMVar_hsa_circ_206745,RMVar_hsa_circ_61971,RMVar_hsa_circ_206743,RMVar_hsa_circ_364051,RMVar_hsa_circ_56153 84851 RMVar_ID_84851 Human_SNP_ID_112626074 m1A Human chr2 - 215397188 215397188 215397188 TGTCTCCACCAACAAACTTGCATCTGGAGGCAAACCCTGACACTGGAGTGCTCACAGTCTCCTGG TGTCTCCACCAACAAACTTGCATCTGGAGGCAGACCCTGACACTGGAGTGCTCACAGTCTCCTGG T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215394541..215399272 32194978 MeRIP-seq:(Medium) rs746992481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142813,Human_RBP_ID_775175,Human_RBP_ID_829302,Human_RBP_ID_921731,Human_RBP_ID_5239710,Human_RBP_ID_17279313,Human_RBP_ID_17698346,Human_RBP_ID_17965699,Human_RBP_ID_22450725,Human_RBP_ID_22765242 Human_Splice_Rec_355070,Human_Splice_Rec_355071,Human_Splice_Rec_355158,Human_Splice_Rec_355159,Human_Splice_Rec_355248,Human_Splice_Rec_355249,Human_Splice_Rec_355340,Human_Splice_Rec_355341,Human_Splice_Rec_355430,Human_Splice_Rec_355431,Human_Splice_Rec_355516,Human_Splice_Rec_355517,Human_Splice_Rec_355640,Human_Splice_Rec_355641,Human_Splice_Rec_355730,Human_Splice_Rec_355731,Human_Splice_Rec_355818,Human_Splice_Rec_355819,Human_Splice_Rec_355908,Human_Splice_Rec_355909 Human_miRNA_ID_2174461,Human_miRNA_ID_2174462,Human_miRNA_ID_2177905,Human_miRNA_ID_2177906 RMVar_hsa_circ_23898,RMVar_hsa_circ_3650,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_63624,RMVar_hsa_circ_79478,RMVar_hsa_circ_265376,RMVar_hsa_circ_122684,RMVar_hsa_circ_88845,RMVar_hsa_circ_206721,RMVar_hsa_circ_206722,RMVar_hsa_circ_206723,RMVar_hsa_circ_53921,RMVar_hsa_circ_81432,RMVar_hsa_circ_206727,RMVar_hsa_circ_380,RMVar_hsa_circ_120836,RMVar_hsa_circ_93135,RMVar_hsa_circ_121202,RMVar_hsa_circ_206728,RMVar_hsa_circ_206729,RMVar_hsa_circ_123745,RMVar_hsa_circ_113512,RMVar_hsa_circ_23850,RMVar_hsa_circ_206733,RMVar_hsa_circ_206734,RMVar_hsa_circ_206735,RMVar_hsa_circ_37635,RMVar_hsa_circ_112126,RMVar_hsa_circ_56306,RMVar_hsa_circ_206738,RMVar_hsa_circ_45854,RMVar_hsa_circ_51496,RMVar_hsa_circ_30025,RMVar_hsa_circ_110836,RMVar_hsa_circ_39583,RMVar_hsa_circ_101080,RMVar_hsa_circ_268941,RMVar_hsa_circ_206741,RMVar_hsa_circ_269134,RMVar_hsa_circ_266791,RMVar_hsa_circ_206742,RMVar_hsa_circ_100587,RMVar_hsa_circ_116298,RMVar_hsa_circ_206744,RMVar_hsa_circ_64680,RMVar_hsa_circ_206745,RMVar_hsa_circ_61971,RMVar_hsa_circ_375535,RMVar_hsa_circ_63479,RMVar_hsa_circ_358981,RMVar_hsa_circ_117625,RMVar_hsa_circ_206747,RMVar_hsa_circ_206748,RMVar_hsa_circ_370112,RMVar_hsa_circ_330683,RMVar_hsa_circ_206750,RMVar_hsa_circ_66168,RMVar_hsa_circ_85394,RMVar_hsa_circ_64362,RMVar_hsa_circ_206751,RMVar_hsa_circ_53859 84852 RMVar_ID_84852 Human_SNP_ID_112629467 m1A Human chr2 + 215409600 215409600 215409600 TACTGTGGCTCATCTCCCTCCTCACTCAGCTCATATTCCACCCGGAATCCCGACACGGTGTCGGA TACTGTGGCTCATCTCCCTCCTCACTCAGCTCGTATTCCACCCGGAATCCCGACACGGTGTCGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215407155..215409777 32194978 MeRIP-seq:(Medium) rs1236701823 Functional Loss SNV dbSNP153 33..33 33 - - - 84853 RMVar_ID_84853 Human_SNP_ID_112629668 m1A Human chr2 + 215410169 215410168 215410170 ACACACACACACACACGTGTTTACAAGGATGAACATTTGAAGATGATGTTCAGTAATCTTCAAAG ACACACACACACACACGTGTTTACAAGGATGA__ATTTGAAGATGATGTTCAGTAATCTTCAAAG AAC A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215409926..215414722 32194978 MeRIP-seq:(Medium) rs368396154 Functional Loss DEL dbSNP153 33..34 33 - - - 84854 RMVar_ID_84854 Human_SNP_ID_112636451 m1A Human chr2 - 215436004 215436004 215436004 GAGGGAACCCCAGGCGCGAGCGGGAAGAGGGGACCTGCAGCCACAACTTCTCTGGTCCTCTGCAT GAGGGAACCCCAGGCGCGAGCGGGAAGAGGGGCCCTGCAGCCACAACTTCTCTGGTCCTCTGCAT T G FN1 Ensembl:ENSG00000115414 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:215435956..215436041 26863196 MeRIP-seq:(Medium) rs973946206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142827,Human_RBP_ID_778001,Human_RBP_ID_4595664,Human_RBP_ID_5528179,Human_RBP_ID_6886179,Human_RBP_ID_22450820 Human_miRNA_ID_2566255 RMVar_hsa_circ_116298,RMVar_hsa_circ_206745,RMVar_hsa_circ_88129,RMVar_hsa_circ_206757,RMVar_hsa_circ_87667,RMVar_hsa_circ_206764,RMVar_hsa_circ_79733,RMVar_hsa_circ_206775 84855 RMVar_ID_84855 Human_SNP_ID_112775976 m1A Human chr2 - 216013537 216013537 216013537 GGGAAAAAAAGCCCGAAGAAAACTCACGCCCCAAACAAAACGCAAGGAGAGGAGGGCGCGCGGCC GGGAAAAAAAGCCCGAAGAAAACTCACGCCCCGAACAAAACGCAAGGAGAGGAGGGCGCGCGGCC T C MREG,PECR Ensembl:ENSG00000118242,Ensembl:ENSG00000115425 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:216013415..216013553 26863196 MeRIP-seq:(Medium) rs1368000736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9385406 RMVar_hsa_circ_93943,RMVar_hsa_circ_206796 84856 RMVar_ID_84856 Human_SNP_ID_112793574 m1A Human chr2 - 216081725 216081725 216081725 GCACCCCGCTGCAGGGATGGCCTCCTGGGCTAAGGGCAGGAGCTACCTGGCGCCTGGTTTGCTGC GCACCCCGCTGCAGGGATGGCCTCCTGGGCTAGGGGCAGGAGCTACCTGGCGCCTGGTTTGCTGC T C PECR Ensembl:ENSG00000115425 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:216081674..216081770 26863196 MeRIP-seq:(Medium) rs1418019720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9064,Human_RBP_ID_4622858,Human_RBP_ID_18422014,Human_RBP_ID_22451892,Human_RBP_ID_23852489 84857 RMVar_ID_84857 Human_SNP_ID_112800382 m1A Human chr2 + 216109456 216109456 216109456 GAGGACCGGCAACATGGTGCGGTCGGGGAATAAGGTATAAAGAAAGCCATGGACTTGGGCTTTAC GAGGACCGGCAACATGGTGCGGTCGGGGAATACGGTATAAAGAAAGCCATGGACTTGGGCTTTAC A C XRCC5 Ensembl:ENSG00000079246 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:216109430..216109608 26863196 MeRIP-seq:(Medium) rs76527766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_145778,Human_RBP_ID_4623833,Human_RBP_ID_5381947,Human_RBP_ID_8852188,Human_RBP_ID_13766073,Human_RBP_ID_19102660,Human_RBP_ID_26338775 Human_Splice_Rec_356441,Human_Splice_Rec_356481,Human_Splice_Rec_356489,Human_Splice_Rec_356493,Human_Splice_Rec_356533 84858 RMVar_ID_84858 Human_SNP_ID_112801345 m1A Human chr2 + 216113002 216113002 216113002 TCTTACGACTTATTTTCTCAAACACTCTTTGGAACTTTGTTTCCAGGCAGCTGTTGTGCTGTGTA TCTTACGACTTATTTTCTCAAACACTCTTTGGGACTTTGTTTCCAGGCAGCTGTTGTGCTGTGTA A G XRCC5 Ensembl:ENSG00000079246 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:216113001..216113050 26863196 MeRIP-seq:(Medium) rs1162610789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4630043 84859 RMVar_ID_84859 Human_SNP_ID_112808657 m1A Human chr2 - 216141316 216141316 216141316 ATATGACTTGTTCATCCTTCTTCTCTTACCTGAAATAATCTCTGAAATCGAGGATTTGGGATTTT ATATGACTTGTTCATCCTTCTTCTCTTACCTGGAATAATCTCTGAAATCGAGGATTTGGGATTTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:216141301..216141325 26863196 MeRIP-seq:(Medium) rs41257924 Functional Loss SNV dbSNP153 33..33 33 - - - 84860 RMVar_ID_84860 Human_SNP_ID_112824697 m1A Human chr2 + 216204392 216204392 216204392 AGCTGTATTTGAAGAAGGTGGTGATGTGGACGATTTAGTAAGTACTTTTAATATGCACCTGGTGT AGCTGTATTTGAAGAAGGTGGTGATGTGGACGGTTTAGTAAGTACTTTTAATATGCACCTGGTGT A G XRCC5 Ensembl:ENSG00000079246 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:216204281..216204449 26863196 MeRIP-seq:(Medium) rs1361665582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1910988,Human_RBP_ID_5118130,Human_RBP_ID_6887103,Human_RBP_ID_8512129,Human_RBP_ID_9385455,Human_RBP_ID_22452638,Human_RBP_ID_23852799,Human_RBP_ID_26340272 Human_Splice_Rec_356478,Human_Splice_Rec_356479,Human_Splice_Rec_356530,Human_Splice_Rec_356531,Human_Splice_Rec_356580,Human_Splice_Rec_356581,Human_Splice_Rec_356595 RMVar_hsa_circ_119223,RMVar_hsa_circ_206819,RMVar_hsa_circ_84306,RMVar_hsa_circ_206824,RMVar_hsa_circ_98557,RMVar_hsa_circ_206827,RMVar_hsa_circ_89378,RMVar_hsa_circ_206829,RMVar_hsa_circ_90117,RMVar_hsa_circ_206833,RMVar_hsa_circ_206837,RMVar_hsa_circ_101558,RMVar_hsa_circ_206839,RMVar_hsa_circ_371941,RMVar_hsa_circ_206844 84861 RMVar_ID_84861 Human_SNP_ID_112824931 m1A Human chr2 + 216205298 216205298 216205298 ACAAGTTGGATGCGGCCATTCAAGGGGAGCCAAAATCTCAAGAAATTCCCAGCAGGTTACCTGGA ACAAGTTGGATGCGGCCATTCAAGGGGAGCCAGAATCTCAAGAAATTCCCAGCAGGTTACCTGGA A G XRCC5 Ensembl:ENSG00000079246 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:216204319..216205509 32194978 MeRIP-seq:(Medium) rs547874427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_543986,Human_RBP_ID_1021921,Human_RBP_ID_1910992,Human_RBP_ID_5118131,Human_RBP_ID_5197848,Human_RBP_ID_9102891,Human_RBP_ID_9385457,Human_RBP_ID_17275012,Human_RBP_ID_17390240,Human_RBP_ID_17505936,Human_RBP_ID_17658214,Human_RBP_ID_17950300,Human_RBP_ID_20437132,Human_RBP_ID_22505053,Human_RBP_ID_26338796,Human_RBP_ID_26819204,Human_RBP_ID_27286442,Human_RBP_ID_27692602 Human_miRNA_ID_2864793 RMVar_hsa_circ_84306,RMVar_hsa_circ_206824,RMVar_hsa_circ_98557,RMVar_hsa_circ_206827,RMVar_hsa_circ_89378,RMVar_hsa_circ_206829,RMVar_hsa_circ_90117,RMVar_hsa_circ_206833,RMVar_hsa_circ_206837,RMVar_hsa_circ_101558,RMVar_hsa_circ_206844,RMVar_hsa_circ_206845,RMVar_hsa_circ_117022 84862 RMVar_ID_84862 Human_SNP_ID_112896654 m1A Human chr2 + 216498875 216498875 216498875 CCTTTCTGGGCTCGGACCTAGGTCGCGGCGACATGGTGAGTGTGGGTCTCTGTGCGGCCTAGAAC CCTTTCTGGGCTCGGACCTAGGTCGCGGCGACGTGGTGAGTGTGGGTCTCTGTGCGGCCTAGAAC A G RPL37A Ensembl:ENSG00000197756 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:216498826..216498900 26863196 MeRIP-seq:(Medium) rs1487469004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242140,Human_RBP_ID_776628,Human_RBP_ID_828667,Human_RBP_ID_923249,Human_RBP_ID_1299559,Human_RBP_ID_4622859,Human_RBP_ID_5146678,Human_RBP_ID_5197850,Human_RBP_ID_5444472,Human_RBP_ID_17657489,Human_RBP_ID_19102681,Human_RBP_ID_22450077,Human_RBP_ID_26819208 Human_Splice_Rec_356765,Human_Splice_Rec_356769,Human_Splice_Rec_356771,Human_Splice_Rec_356777,Human_Splice_Rec_356783,Human_Splice_Rec_356789 RMVar_hsa_circ_84542,RMVar_hsa_circ_206860 84863 RMVar_ID_84863 Human_SNP_ID_112896657 m1A Human chr2 - 216498879 216498879 216498879 TAGAGTTCTAGGCCGCACAGAGACCCACACTCACCATGTCGCCGCGACCTAGGTCCGAGCCCAGA TAGAGTTCTAGGCCGCACAGAGACCCACACTCTCCATGTCGCCGCGACCTAGGTCCGAGCCCAGA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr2:216498851..216498993;chr2:216498851..216498900 26863196,32194978 MeRIP-seq:(Medium) rs112080422 Functional Loss SNV dbSNP153 33..33 33 - - - 84864 RMVar_ID_84864 Human_SNP_ID_112896658 m1A Human chr2 - 216498879 216498879 216498879 TAGAGTTCTAGGCCGCACAGAGACCCACACTCACCATGTCGCCGCGACCTAGGTCCGAGCCCAGA TAGAGTTCTAGGCCGCACAGAGACCCACACTCGCCATGTCGCCGCGACCTAGGTCCGAGCCCAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr2:216498851..216498993;chr2:216498851..216498900 26863196,32194978 MeRIP-seq:(Medium) rs112080422 Functional Loss SNV dbSNP153 33..33 33 - - - 84865 RMVar_ID_84865 Human_SNP_ID_112896659 m1A Human chr2 - 216498879 216498879 216498879 TAGAGTTCTAGGCCGCACAGAGACCCACACTCACCATGTCGCCGCGACCTAGGTCCGAGCCCAGA TAGAGTTCTAGGCCGCACAGAGACCCACACTCCCCATGTCGCCGCGACCTAGGTCCGAGCCCAGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr2:216498851..216498993;chr2:216498851..216498900 26863196,32194978 MeRIP-seq:(Medium) rs112080422 Functional Loss SNV dbSNP153 33..33 33 - - - 84866 RMVar_ID_84866 Human_SNP_ID_112896858 m1A Human chr2 + 216499356 216499356 216499356 GCCTCCCTCCGGAAAATGGTGAAGAAAATTGAAATCAGCCAGCACGCCAAGTACACTTGCTCTTT GCCTCCCTCCGGAAAATGGTGAAGAAAATTGAGATCAGCCAGCACGCCAAGTACACTTGCTCTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:216499251..216499400 32194978 MeRIP-seq:(Medium) rs770037592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243226,Human_RBP_ID_544041,Human_RBP_ID_828670,Human_RBP_ID_923550,Human_RBP_ID_1194820,Human_RBP_ID_1299560,Human_RBP_ID_1583409,Human_RBP_ID_1911031,Human_RBP_ID_2623156,Human_RBP_ID_3615842,Human_RBP_ID_4630111,Human_RBP_ID_5146681,Human_RBP_ID_8512190,Human_RBP_ID_9102940,Human_RBP_ID_13769991,Human_RBP_ID_17275047,Human_RBP_ID_17392869,Human_RBP_ID_18754534,Human_RBP_ID_22073894,Human_RBP_ID_22505057,Human_RBP_ID_22814726,Human_RBP_ID_26479682,Human_RBP_ID_27006838,Human_RBP_ID_27286471,Human_RBP_ID_27477547 Human_Splice_Rec_356763,Human_Splice_Rec_356766,Human_Splice_Rec_356767,Human_Splice_Rec_356770,Human_Splice_Rec_356772,Human_Splice_Rec_356773,Human_Splice_Rec_356778,Human_Splice_Rec_356779,Human_Splice_Rec_356784,Human_Splice_Rec_356785,Human_Splice_Rec_356790,Human_Splice_Rec_356791,Human_Splice_Rec_356797,Human_Splice_Rec_356802,Human_Splice_Rec_356803,Human_Splice_Rec_356807,Human_Splice_Rec_356815,Human_Splice_Rec_356822,Human_Splice_Rec_356823 Human_miRNA_ID_2330427,Human_miRNA_ID_2963507 RMVar_hsa_circ_103123,RMVar_hsa_circ_84542,RMVar_hsa_circ_330535,RMVar_hsa_circ_206860,RMVar_hsa_circ_267564,RMVar_hsa_circ_206861 84867 RMVar_ID_84867 Human_SNP_ID_112896859 m1A Human chr2 + 216499356 216499356 216499356 GCCTCCCTCCGGAAAATGGTGAAGAAAATTGAAATCAGCCAGCACGCCAAGTACACTTGCTCTTT GCCTCCCTCCGGAAAATGGTGAAGAAAATTGATATCAGCCAGCACGCCAAGTACACTTGCTCTTT A T RPL37A Ensembl:ENSG00000197756 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:216499251..216499400 32194978 MeRIP-seq:(Medium) rs770037592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243226,Human_RBP_ID_544041,Human_RBP_ID_828670,Human_RBP_ID_923550,Human_RBP_ID_1194820,Human_RBP_ID_1299560,Human_RBP_ID_1583409,Human_RBP_ID_1911031,Human_RBP_ID_2623156,Human_RBP_ID_3615842,Human_RBP_ID_4630111,Human_RBP_ID_5146681,Human_RBP_ID_8512190,Human_RBP_ID_9102940,Human_RBP_ID_13769991,Human_RBP_ID_17275047,Human_RBP_ID_17392869,Human_RBP_ID_18754534,Human_RBP_ID_22073894,Human_RBP_ID_22505057,Human_RBP_ID_22814726,Human_RBP_ID_26479682,Human_RBP_ID_27006838,Human_RBP_ID_27286471,Human_RBP_ID_27477547 Human_Splice_Rec_356763,Human_Splice_Rec_356766,Human_Splice_Rec_356767,Human_Splice_Rec_356770,Human_Splice_Rec_356772,Human_Splice_Rec_356773,Human_Splice_Rec_356778,Human_Splice_Rec_356779,Human_Splice_Rec_356784,Human_Splice_Rec_356785,Human_Splice_Rec_356790,Human_Splice_Rec_356791,Human_Splice_Rec_356797,Human_Splice_Rec_356802,Human_Splice_Rec_356803,Human_Splice_Rec_356807,Human_Splice_Rec_356815,Human_Splice_Rec_356822,Human_Splice_Rec_356823 Human_miRNA_ID_2330427,Human_miRNA_ID_2963507 RMVar_hsa_circ_103123,RMVar_hsa_circ_84542,RMVar_hsa_circ_330535,RMVar_hsa_circ_206860,RMVar_hsa_circ_267564,RMVar_hsa_circ_206861 84868 RMVar_ID_84868 Human_SNP_ID_112897075 m1A Human chr2 + 216499928 216499928 216499928 TGTAAGAGAAAATACTTACTTGGTTCATAGTGAAAATTGGTTCTCTTTTATAGACCAAGATGAAG TGTAAGAGAAAATACTTACTTGGTTCATAGTGCAAATTGGTTCTCTTTTATAGACCAAGATGAAG A C RPL37A Ensembl:ENSG00000197756 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:216499926..216499975;chr2:216499926..216499950 26863196 MeRIP-seq:(Medium) rs111309414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_356792 RMVar_hsa_circ_103123,RMVar_hsa_circ_84542,RMVar_hsa_circ_330535,RMVar_hsa_circ_206860,RMVar_hsa_circ_206861 84869 RMVar_ID_84869 Human_SNP_ID_112897076 m1A Human chr2 + 216499928 216499928 216499928 TGTAAGAGAAAATACTTACTTGGTTCATAGTGAAAATTGGTTCTCTTTTATAGACCAAGATGAAG TGTAAGAGAAAATACTTACTTGGTTCATAGTGGAAATTGGTTCTCTTTTATAGACCAAGATGAAG A G RPL37A Ensembl:ENSG00000197756 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:216499926..216499975;chr2:216499926..216499950 26863196 MeRIP-seq:(Medium) rs111309414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_356792 RMVar_hsa_circ_103123,RMVar_hsa_circ_84542,RMVar_hsa_circ_330535,RMVar_hsa_circ_206860,RMVar_hsa_circ_206861 84870 RMVar_ID_84870 Human_SNP_ID_112897135 m1A Human chr2 - 216500033 216500033 216500033 CACACTTCCAAATACCACAAGGAACTAGACTCACTTGTACGTCCAGGCACCGCCAGCCACTGTCT CACACTTCCAAATACCACAAGGAACTAGACTCCCTTGTACGTCCAGGCACCGCCAGCCACTGTCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:216499890..216500083 26863410 MeRIP-seq:(Medium) rs1559145038 Functional Loss SNV dbSNP153 33..33 33 - - - 84871 RMVar_ID_84871 Human_SNP_ID_112897701 m1A Human chr2 + 216501857 216501857 216501857 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGCACCACCATACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCACGCACCACCATACCTGGCTAATTTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1344705061 Functional Loss SNV dbSNP153 33..33 33 - - - 84872 RMVar_ID_84872 Human_SNP_ID_112929658 m1A Human chr2 - 216633552 216633552 216633552 GCAGCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGCGCGGGGCAGCCCACTCTCGGCAGCATGCTG GCAGCGGCAGCAGCGGCGGCGGCGGCAGCGGCGGCGCGGGGCAGCCCACTCTCGGCAGCATGCTG T C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr2:216633455..216633655 26863410 MeRIP-seq:(Medium) rs370345120 Functional Loss SNV dbSNP153 33..33 33 - - - 84873 RMVar_ID_84873 Human_SNP_ID_112929709 m1A Human chr2 - 216633582 216633582 216633582 CGCCGCCACTCGCGCCCAGTAGCAGCAGCAGCAGCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGC CGCCGCCACTCGCGCCCAGTAGCAGCAGCAGCGGCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:216633421..216633655 26863410 MeRIP-seq:(Medium) rs757848711 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 84874 RMVar_ID_84874 Human_SNP_ID_112940896 m1A Human chr2 - 216676432 216676432 216676432 GAAGAGAAGGGAAGGAAGTGTTTGTGTAGAAGAGAGAGAAAGACGAATAGAGTTAGGAAAAGGAA GAAGAGAAGGGAAGGAAGTGTTTGTGTAGAAGGGAGAGAAAGACGAATAGAGTTAGGAAAAGGAA T C IGFBP5 Ensembl:ENSG00000115461 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:216676341..216676473 26863196 MeRIP-seq:(Medium) rs1022065308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17698474 RMVar_hsa_circ_102467,RMVar_hsa_circ_119356,RMVar_hsa_circ_206867,RMVar_hsa_circ_206868 84875 RMVar_ID_84875 Human_SNP_ID_113115065 m1A Human chr2 - 217364438 217364438 217364438 TGGTGAAGATGATGATGGTGGTGATGATGGTGATGGTGATGATGATGATGATGACAATGGTGATG TGGTGAAGATGATGATGGTGGTGATGATGGTGTTGGTGATGATGATGATGATGACAATGGTGATG T A DIRC3 Ensembl:ENSG00000231672 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217364388..217364464 26863196 MeRIP-seq:(Medium) rs1006164150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71298 84876 RMVar_ID_84876 Human_SNP_ID_113115066 m1A Human chr2 - 217364438 217364438 217364438 TGGTGAAGATGATGATGGTGGTGATGATGGTGATGGTGATGATGATGATGATGACAATGGTGATG TGGTGAAGATGATGATGGTGGTGATGATGGTGGTGGTGATGATGATGATGATGACAATGGTGATG T C DIRC3 Ensembl:ENSG00000231672 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217364388..217364464 26863196 MeRIP-seq:(Medium) rs1006164150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71298 84877 RMVar_ID_84877 Human_SNP_ID_113218517 m1A Human chr2 + 217801356 217801356 217801356 ACGTGGAGCTCACTGGGCCCCTCCCCCAGCTGAAGGGACATGACCCTCCTCTGCCCTCTTCCCTC ACGTGGAGCTCACTGGGCCCCTCCCCCAGCTGCAGGGACATGACCCTCCTCTGCCCTCTTCCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:217801307..217801462 26863196 MeRIP-seq:(Medium) rs76591402 Functional Loss SNV dbSNP153 33..33 33 - - - 84878 RMVar_ID_84878 Human_SNP_ID_113219214 m1A Human chr2 - 217804249 217804249 217804249 AGAGAGAGAGAGAGAGAGAGAGAGAAAGATGGAGGAGAAGAACTTGGATTCCCCTGGGTAGATGG AGAGAGAGAGAGAGAGAGAGAGAGAAAGATGGCGGAGAAGAACTTGGATTCCCCTGGGTAGATGG T G TNS1 Ensembl:ENSG00000079308 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217804198..217804325 26863196 MeRIP-seq:(Medium) rs1199688044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146944 RMVar_hsa_circ_206876,RMVar_hsa_circ_113737 84879 RMVar_ID_84879 Human_SNP_ID_113219217 m1A Human chr2 - 217804255 217804252 217804256 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGATGGAGGAGAAGAACTTGGATTCCCCTGGGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA____TGGAGGAGAAGAACTTGGATTCCCCTGGGT ATCTT A TNS1 Ensembl:ENSG00000079308 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:217804206..217804346 26863196 MeRIP-seq:(Medium) rs1215451079 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5147212 RMVar_hsa_circ_206876,RMVar_hsa_circ_113737 84880 RMVar_ID_84880 Human_SNP_ID_113219816 m1A Human chr2 + 217805681 217805678 217805682 CACACACAACACACATATCACCACACACATACACACCATCACACACATCACCACATGCATACACC CACACACAACACACATATCACCACACACAT____ACCATCACACACATCACCACATGCATACACC TACAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217805524..217805873 26863196 MeRIP-seq:(Medium) rs1270469127 Functional Loss DEL dbSNP153 31..34 33 - - - 84881 RMVar_ID_84881 Human_SNP_ID_113229834 m1A Human chr2 - 217843634 217843634 217843634 CAGCCTGAAGAGATCATGAGGAGGACTGAGAAAAATCCACTGGGCTTGCAAATTAGGCAGCCCTG CAGCCTGAAGAGATCATGAGGAGGACTGAGAAGAATCCACTGGGCTTGCAAATTAGGCAGCCCTG T C TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217843632..217844037 26863196 MeRIP-seq:(Medium) rs1016870756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206876,RMVar_hsa_circ_113737,RMVar_hsa_circ_65689,RMVar_hsa_circ_364142 84882 RMVar_ID_84882 Human_SNP_ID_113233029 m1A Human chr2 - 217855232 217855232 217855232 AGCATATGAAGAGTTGAGTAGGAGTAGAGTGGAGGGTGTTCTGGGTATGGAGGACAAGGAAGTGA AGCATATGAAGAGTTGAGTAGGAGTAGAGTGGTGGGTGTTCTGGGTATGGAGGACAAGGAAGTGA T A TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:217855230..217855343 26863196 MeRIP-seq:(Medium) rs910477527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206876,RMVar_hsa_circ_113737,RMVar_hsa_circ_118357,RMVar_hsa_circ_206879 84883 RMVar_ID_84883 Human_SNP_ID_113234004 m1A Human chr2 + 217858962 217858962 217858962 GCCCAGTCCAACTCCAGCCCCAACCCCAGCCCAGCCCCAGCCCCAGCCCCAGCCCCTGCTCAACT GCCCAGTCCAACTCCAGCCCCAACCCCAGCCCCGCCCCAGCCCCAGCCCCAGCCCCTGCTCAACT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:217858946..217859075 26863196 MeRIP-seq:(Medium) rs1386909502 Functional Loss SNV dbSNP153 33..33 33 - - - 84884 RMVar_ID_84884 Human_SNP_ID_113234678 m1A Human chr2 - 217861831 217861831 217861831 TACTGCTCAGGGGGCACAGGGCTAGGGAAGGGAGACGGGGAAGCCCACGCTGCACTACTCGTGTT TACTGCTCAGGGGGCACAGGGCTAGGGAAGGGGGACGGGGAAGCCCACGCTGCACTACTCGTGTT T C TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217861824..217861960 26863196 MeRIP-seq:(Medium) rs1434361981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206876,RMVar_hsa_circ_113737,RMVar_hsa_circ_118357,RMVar_hsa_circ_206879 84885 RMVar_ID_84885 Human_SNP_ID_113245114 m1A Human chr2 - 217904450 217904450 217904450 ACCTAATTTGTAAGGCTCCTGTCACCTGTCTCAGGTTGGGTTGGCTCCAGGGTCATTGAGCCAGT ACCTAATTTGTAAGGCTCCTGTCACCTGTCTCGGGTTGGGTTGGCTCCAGGGTCATTGAGCCAGT T C TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217904421..217904594 26863196 MeRIP-seq:(Medium) rs976753025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118357,RMVar_hsa_circ_354231,RMVar_hsa_circ_206879,RMVar_hsa_circ_365632,RMVar_hsa_circ_8652,RMVar_hsa_circ_320366,RMVar_hsa_circ_67307,RMVar_hsa_circ_9741,RMVar_hsa_circ_206883,RMVar_hsa_circ_96893 84886 RMVar_ID_84886 Human_SNP_ID_113245509 m1A Human chr2 + 217906037 217906037 217906037 AGCCCTCGGTTTCCCTTGCTGTGGTTTTGCGCATTTCCCCTTGATCCCCATGGCCACTCATCACA AGCCCTCGGTTTCCCTTGCTGTGGTTTTGCGCCTTTCCCCTTGATCCCCATGGCCACTCATCACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217906009..217906082 26863196 MeRIP-seq:(Medium) rs1158967236 Functional Loss SNV dbSNP153 33..33 33 - - - 84887 RMVar_ID_84887 Human_SNP_ID_113260746 m1A Human chr2 + 217965781 217965781 217965781 TAGCCAGCTCAACGGGCACCACAGACCCCCCGAGCTAGAAGCCAGAAGCAGCCAGGGTGGCTGGT TAGCCAGCTCAACGGGCACCACAGACCCCCCGGGCTAGAAGCCAGAAGCAGCCAGGGTGGCTGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:217965776..217966060 26863196 MeRIP-seq:(Medium) rs1380804544 Functional Loss SNV dbSNP153 33..33 33 - - - 84888 RMVar_ID_84888 Human_SNP_ID_113263220 m1A Human chr2 + 217975943 217975943 217975943 GGCCAGAGTGGCCTTCTCAGAGTGGAAATCCAATCGCGTCCCTCCAGCCCAAACTCCCCAGCACT GGCCAGAGTGGCCTTCTCAGAGTGGAAATCCACTCGCGTCCCTCCAGCCCAAACTCCCCAGCACT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:217975941..217976172 26863196 MeRIP-seq:(Medium) rs1019416393 Functional Loss SNV dbSNP153 33..33 33 - - - 84889 RMVar_ID_84889 Human_SNP_ID_113263221 m1A Human chr2 + 217975943 217975943 217975943 GGCCAGAGTGGCCTTCTCAGAGTGGAAATCCAATCGCGTCCCTCCAGCCCAAACTCCCCAGCACT GGCCAGAGTGGCCTTCTCAGAGTGGAAATCCAGTCGCGTCCCTCCAGCCCAAACTCCCCAGCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:217975941..217976172 26863196 MeRIP-seq:(Medium) rs1019416393 Functional Loss SNV dbSNP153 33..33 33 - - - 84890 RMVar_ID_84890 Human_SNP_ID_113266165 m1A Human chr2 + 217988037 217988037 217988037 CCTGGAGATCCCAGTCCCTTTGCTGAGGCTGCACACATGACCTATAGAGTCAGGAGTCTTCCTCC CCTGGAGATCCCAGTCCCTTTGCTGAGGCTGCGCACATGACCTATAGAGTCAGGAGTCTTCCTCC A G AC010136.1 Ensembl:ENSG00000223923 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217988006..217988212 26863196 MeRIP-seq:(Medium) rs1177734702 Functional Loss SNV dbSNP153 33..33 33 - - - 84891 RMVar_ID_84891 Human_SNP_ID_113266327 m1A Human chr2 + 217988746 217988746 217988746 TGATTTTGGTATTGCAAAAGTCCTGGTTAGCCACTTTCCCTCCCCCTGAGAGCCCACGTCCTGAA TGATTTTGGTATTGCAAAAGTCCTGGTTAGCCCCTTTCCCTCCCCCTGAGAGCCCACGTCCTGAA A C AC010136.1 Ensembl:ENSG00000223923 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:217988742..217988821 26863196 MeRIP-seq:(Medium) rs1296891401 Functional Loss SNV dbSNP153 33..33 33 - - - 84892 RMVar_ID_84892 Human_SNP_ID_113269324 m1A Human chr2 - 218001458 218001458 218001458 CAAGAAGGATGGCAGGTAGACCTCCAGGGGTGACGAGCTGCTGTGACTGGAGAGAGGGCTCTATA CAAGAAGGATGGCAGGTAGACCTCCAGGGGTGTCGAGCTGCTGTGACTGGAGAGAGGGCTCTATA T A TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218001455..218001848 26863196 MeRIP-seq:(Medium) rs1025747785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126758,RMVar_hsa_circ_206886 84893 RMVar_ID_84893 Human_SNP_ID_113269758 m1A Human chr2 - 218002958 218002908 218002958 CTGGCGGAGCCGGAGCAGCCGCGGACTCAGAGAGCCCTTCTGCCAGCGCCGCGGGGACTCTAGCT CTGGCGGAGCCGGAGCAGCCGCGGACTCAGAG_________________________________ CCTGTGAAGAGCCCCTGAAGCTAGAGTCCCCGCGGCGCTGGCAGAAGGGCT C TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218002908..218002993 26863196 MeRIP-seq:(Medium) rs1318033629 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_126758,RMVar_hsa_circ_206886 84894 RMVar_ID_84894 Human_SNP_ID_113270009 m1A Human chr2 + 218003663 218003663 218003663 TTTTCCCCCTTCTTTCTTTCTTTCCTGCAAACATCTGTCCCAGCCTTTCCTGCCCTTCTGAAAGG TTTTCCCCCTTCTTTCTTTCTTTCCTGCAAACGTCTGTCCCAGCCTTTCCTGCCCTTCTGAAAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218003613..218003720 26863196 MeRIP-seq:(Medium) rs367784635 Functional Loss SNV dbSNP153 33..33 33 - - - 84895 RMVar_ID_84895 Human_SNP_ID_113270010 m1A Human chr2 - 218003666 218003666 218003666 CTCCCTTTCAGAAGGGCAGGAAAGGCTGGGACAGATGTTTGCAGGAAAGAAAGAAAGAAGGGGGA CTCCCTTTCAGAAGGGCAGGAAAGGCTGGGACGGATGTTTGCAGGAAAGAAAGAAAGAAGGGGGA T C TNS1 Ensembl:ENSG00000079308 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:218003615..218003699 26863196 MeRIP-seq:(Medium) rs1425794368 Functional Loss SNV dbSNP153 33..33 33 - - - 84896 RMVar_ID_84896 Human_SNP_ID_113324424 m1A Human chr2 - 218216543 218216543 218216543 GAGAGGATCAGAGTAGGGATGCGGAAGCAGCGAGTGGTCAGGAGTGTGCGTGCCAAAAGGCAGGA GAGAGGATCAGAGTAGGGATGCGGAAGCAGCGGGTGGTCAGGAGTGTGCGTGCCAAAAGGCAGGA T C lnc-AAMP-2,lnc-AAMP-2:2,lnc-AAMP-2:3,lnc-AAMP-2:4,lnc-AAMP-2:5,lnc-AAMP-2:6,lnc-AAMP-2:7,lnc-AAMP-2:8,lnc-AAMP-2:9 RNACentral:URS0000D59B7A,RNACentral:URS0000D5771B,RNACentral:URS00008B53C5,RNACentral:URS0000D5A23D,RNACentral:URS00009B0001,RNACentral:URS0000D5AD7D,RNACentral:URS0000D56E85,RNACentral:URS00009C47B2,RNACentral:URS0000D5DA6E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon,exon,exon,intron,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218216497..218216589 26863196 MeRIP-seq:(Medium) rs1186457981 Functional Loss SNV dbSNP153 33..33 33 - - - 84897 RMVar_ID_84897 Human_SNP_ID_113324524 m1A Human chr2 + 218216979 218216979 218216979 CGCGGGGGACGCACTGGTAGGCGGTAGACGTAAGCGGGGTCGGTGGGAAAGTAGACGGTGGGGCG CGCGGGGGACGCACTGGTAGGCGGTAGACGTAGGCGGGGTCGGTGGGAAAGTAGACGGTGGGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218216930..218217008 26863196 MeRIP-seq:(Medium) rs1300468784 Functional Loss SNV dbSNP153 33..33 33 - - - 84898 RMVar_ID_84898 Human_SNP_ID_113324675 m1A Human chr2 - 218217269 218217269 218217269 CTGGCCCACGCACGCAGACTGTGGAGACACCCACCCACCCAACCGACCTGGCCCCCGAAGCCTGA CTGGCCCACGCACGCAGACTGTGGAGACACCCCCCCACCCAACCGACCTGGCCCCCGAAGCCTGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:218217248..218217430 26863196 MeRIP-seq:(Medium) rs1270986089 Functional Loss SNV dbSNP153 33..33 33 - - - 84899 RMVar_ID_84899 Human_SNP_ID_113331699 m1A Human chr2 + 218245380 218245380 218245380 AACCCTATAGCTTGAGTTGCCACTCATCTTACACCCACTTCTCTTCTGGTTGCTTTTGCTTTGTC AACCCTATAGCTTGAGTTGCCACTCATCTTACTCCCACTTCTCTTCTGGTTGCTTTTGCTTTGTC A T ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218245377..218245591 26863196 MeRIP-seq:(Medium) rs779005609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22547778 RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_47512,RMVar_hsa_circ_206892,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_337918,RMVar_hsa_circ_21239,RMVar_hsa_circ_278921,RMVar_hsa_circ_206893,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_374102,RMVar_hsa_circ_206895 84900 RMVar_ID_84900 Human_SNP_ID_113332764 m1A Human chr2 - 218249353 218249353 218249353 TTGGTGTGACGAGGGAACAGCACTGAAGGCGGAAGACACAAACAAGGCGTCAGGACACGACACAA TTGGTGTGACGAGGGAACAGCACTGAAGGCGGTAGACACAAACAAGGCGTCAGGACACGACACAA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:218249351..218249475;chr2:218249351..218249450 32194978 MeRIP-seq:(Medium) rs1350113111 Functional Loss SNV dbSNP153 33..33 33 - - - 84901 RMVar_ID_84901 Human_SNP_ID_113338604 m1A Human chr2 + 218269918 218269918 218269918 AGGGGAGCGGGGAAAAGCAGGAGTCAGAGGCCAGGGGTGAGCGTCTCCTGTCCCATGGCCTGAGG AGGGGAGCGGGGAAAAGCAGGAGTCAGAGGCCGGGGGTGAGCGTCTCCTGTCCCATGGCCTGAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:218269916..218270150 26863196 MeRIP-seq:(Medium) rs1309938807 Functional Loss SNV dbSNP153 33..33 33 - - - 84902 RMVar_ID_84902 Human_SNP_ID_113338900 m1A Human chr2 + 218270567 218270567 218270567 CATGGCGGCGGTGGTAGCTGCTACGGCGCTGAAGGGCCGGGGGGCGAGAAATGCCCGCGTCCTCC CATGGCGGCGGTGGTAGCTGCTACGGCGCTGAGGGGCCGGGGGGCGAGAAATGCCCGCGTCCTCC A G PNKD Ensembl:ENSG00000127838 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:218270526..218270633;chr2:218270501..218270630;chr2:218270526..218270637;chr2:218270476..218270651 26863196 MeRIP-seq:(Medium) rs1159488054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242704,Human_RBP_ID_544282,Human_RBP_ID_4623845,Human_RBP_ID_5118369,Human_RBP_ID_22450081 Human_Splice_Rec_358157,Human_Splice_Rec_358161 RMVar_hsa_circ_206902,RMVar_hsa_circ_110861 84903 RMVar_ID_84903 Human_SNP_ID_113339140 m1A Human chr2 + 218271461 218271457 218271462 GGGCCCTGCAAAGCCACAGCTCCCCAGAGGGCAAGGAGGAACCTGAACCCCTATCCCCGGAGCTG GGGCCCTGCAAAGCCACAGCTCCCCAGAG_____GGAGGAACCTGAACCCCTATCCCCGGAGCTG GGGCAA G PNKD Ensembl:ENSG00000127838 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218271365..218271550 26863196 MeRIP-seq:(Medium) rs747278532 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_544283,Human_RBP_ID_17658704 Human_Splice_Rec_358158,Human_Splice_Rec_358159,Human_Splice_Rec_358162,Human_Splice_Rec_358163,Human_Splice_Rec_358179,Human_Splice_Rec_358181 RMVar_hsa_circ_206902,RMVar_hsa_circ_110861,RMVar_hsa_circ_100101,RMVar_hsa_circ_206903 84904 RMVar_ID_84904 Human_SNP_ID_113339142 m1A Human chr2 + 218271461 218271461 218271461 GGGCCCTGCAAAGCCACAGCTCCCCAGAGGGCAAGGAGGAACCTGAACCCCTATCCCCGGAGCTG GGGCCCTGCAAAGCCACAGCTCCCCAGAGGGCTAGGAGGAACCTGAACCCCTATCCCCGGAGCTG A T PNKD Ensembl:ENSG00000127838 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218271365..218271550 26863196 MeRIP-seq:(Medium) rs780594684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544283,Human_RBP_ID_17658704 Human_Splice_Rec_358158,Human_Splice_Rec_358159,Human_Splice_Rec_358162,Human_Splice_Rec_358163,Human_Splice_Rec_358179,Human_Splice_Rec_358181 Clinvar_Rec_440 RMVar_hsa_circ_206902,RMVar_hsa_circ_110861,RMVar_hsa_circ_100101,RMVar_hsa_circ_206903 84905 RMVar_ID_84905 Human_SNP_ID_113339568 m1A Human chr2 + 218272875 218272875 218272875 ACCAGAGGGCGCATGAAGCCCAGGCTGTTGCCAAACCCTACCCTGCCCCACACCAAGGAGCCAGC ACCAGAGGGCGCATGAAGCCCAGGCTGTTGCCGAACCCTACCCTGCCCCACACCAAGGAGCCAGC A G PNKD Ensembl:ENSG00000127838 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218272765..218272884 26863196 MeRIP-seq:(Medium) rs751019194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544292,Human_RBP_ID_9103037,Human_RBP_ID_17658234,Human_RBP_ID_17950535,Human_RBP_ID_26488214 Human_miRNA_ID_139924,Human_miRNA_ID_416871,Human_miRNA_ID_2131391 RMVar_hsa_circ_206902,RMVar_hsa_circ_110861,RMVar_hsa_circ_100101,RMVar_hsa_circ_206903 84906 RMVar_ID_84906 Human_SNP_ID_113342359 m1A Human chr2 - 218282129 218282129 218282129 CCCTCAGCCCGTGAGCAGCCATGTCCAACCCCAGCGCCCCACCACCATATGAAGACCGCAACCCC CCCTCAGCCCGTGAGCAGCCATGTCCAACCCCCGCGCCCCACCACCATATGAAGACCGCAACCCC T G TMBIM1 Ensembl:ENSG00000135926 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:218282082..218282185 26863196 MeRIP-seq:(Medium) rs1318799737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775705,Human_RBP_ID_830687,Human_RBP_ID_4622866,Human_RBP_ID_5322726,Human_RBP_ID_17392879,Human_RBP_ID_22451920 Human_Splice_Rec_358258,Human_Splice_Rec_358282,Human_Splice_Rec_358360,Human_Splice_Rec_358402,Human_Splice_Rec_358412,Human_Splice_Rec_358418,Human_Splice_Rec_358424,Human_Splice_Rec_358430,Human_Splice_Rec_358434,Human_Splice_Rec_358440,Human_Splice_Rec_358446,Human_Splice_Rec_358448,Human_Splice_Rec_358450 Human_miRNA_ID_2683242 RMVar_hsa_circ_3735,RMVar_hsa_circ_95188,RMVar_hsa_circ_62963,RMVar_hsa_circ_109314,RMVar_hsa_circ_206905,RMVar_hsa_circ_206907,RMVar_hsa_circ_81704,RMVar_hsa_circ_206910,RMVar_hsa_circ_123186,RMVar_hsa_circ_53293,RMVar_hsa_circ_206911,RMVar_hsa_circ_351357 84907 RMVar_ID_84907 Human_SNP_ID_113352208 m1A Human chr2 - 218323341 218323341 218323341 GCGCTCGGCAGCCGCGGGGGCTCACAAGTAGGACGAGGACAAGGACGAGGAGGAGCCAGCAGCCG GCGCTCGGCAGCCGCGGGGGCTCACAAGTAGGGCGAGGACAAGGACGAGGAGGAGCCAGCAGCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:218323293..218323376 26863196 MeRIP-seq:(Medium) rs781485673 Functional Loss SNV dbSNP153 33..33 33 - - - 84908 RMVar_ID_84908 Human_SNP_ID_113356439 m1A Human chr2 - 218340143 218340143 218340143 TCCAGGCACCCCCTGCTCCCTGCCCTCCCCTCACCTGCACAGCCCGAGGGTCTGAAGGGTCCACA TCCAGGCACCCCCTGCTCCCTGCCCTCCCCTCGCCTGCACAGCCCGAGGGTCTGAAGGGTCCACA T C CATIP-AS2 Ensembl:ENSG00000237281 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:218340107..218341537 32194978 MeRIP-seq:(Medium) rs1230004320 Functional Loss SNV dbSNP153 33..33 33 - - - 84909 RMVar_ID_84909 Human_SNP_ID_113356440 m1A Human chr2 - 218340143 218340143 218340143 TCCAGGCACCCCCTGCTCCCTGCCCTCCCCTCACCTGCACAGCCCGAGGGTCTGAAGGGTCCACA TCCAGGCACCCCCTGCTCCCTGCCCTCCCCTCCCCTGCACAGCCCGAGGGTCTGAAGGGTCCACA T G CATIP-AS2 Ensembl:ENSG00000237281 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:218340107..218341537 32194978 MeRIP-seq:(Medium) rs1230004320 Functional Loss SNV dbSNP153 33..33 33 - - - 84910 RMVar_ID_84910 Human_SNP_ID_113373359 m1A Human chr2 - 218398773 218398773 218398773 CTTTTCACTCGTCGTTACTATTTTGTAAGTTCACCATTTAAAAATTAATAATGCCAAGCCCGACA CTTTTCACTCGTCGTTACTATTTTGTAAGTTCGCCATTTAAAAATTAATAATGCCAAGCCCGACA T C AC021016.2 Ensembl:ENSG00000273361 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218398723..218398902 26863196 MeRIP-seq:(Medium) rs1297039585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3148661,Human_miRNA_ID_3164146,Human_miRNA_ID_3200158 84911 RMVar_ID_84911 Human_SNP_ID_113374091 m1A Human chr2 + 218400071 218400071 218400071 GAGGCCGGGCGCCCGGGCCAGAGTCCGGCCGGAGCGGAGCGCGCCCGGCCCCATGGACAGCTCGG GAGGCCGGGCGCCCGGGCCAGAGTCCGGCCGGGGCGGAGCGCGCCCGGCCCCATGGACAGCTCGG A G CTDSP1 Ensembl:ENSG00000144579 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218399881..218400108 26863196 MeRIP-seq:(Medium) rs1161636775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623851 Human_Splice_Rec_358765,Human_Splice_Rec_358777,Human_Splice_Rec_358787,Human_Splice_Rec_358793 RMVar_hsa_circ_96993,RMVar_hsa_circ_268733,RMVar_hsa_circ_98997,RMVar_hsa_circ_206917,RMVar_hsa_circ_206918 84912 RMVar_ID_84912 Human_SNP_ID_113374109 m1A Human chr2 + 218400109 218400109 218400109 GCGCGCCCGGCCCCATGGACAGCTCGGCCGTCATTACTCAGATCAGCAAGGAGGAGGCTCGGGGC GCGCGCCCGGCCCCATGGACAGCTCGGCCGTCGTTACTCAGATCAGCAAGGAGGAGGCTCGGGGC A G CTDSP1 Ensembl:ENSG00000144579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:218400058..218400437 26863196 MeRIP-seq:(Medium) rs919485493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1583480,Human_RBP_ID_4623851,Human_RBP_ID_5422766,Human_RBP_ID_8845695,Human_RBP_ID_26487617,Human_RBP_ID_27477639 Human_Splice_Rec_358765,Human_Splice_Rec_358777,Human_Splice_Rec_358787,Human_Splice_Rec_358793 Human_miRNA_ID_2403156 RMVar_hsa_circ_96993,RMVar_hsa_circ_268733,RMVar_hsa_circ_98997,RMVar_hsa_circ_206917,RMVar_hsa_circ_206918 84913 RMVar_ID_84913 Human_SNP_ID_113374142 m1A Human chr2 + 218400154 218400154 218400154 GCAAGGAGGAGGCTCGGGGCCCGCTGCGGGGCAAAGGTACCGGGGCTGCGGGGAGGGGGCCGAAG GCAAGGAGGAGGCTCGGGGCCCGCTGCGGGGCCAAGGTACCGGGGCTGCGGGGAGGGGGCCGAAG A C CTDSP1 Ensembl:ENSG00000144579 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:218400073..218400373 32194978 MeRIP-seq:(Medium) rs1001911108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776186,Human_RBP_ID_830499,Human_RBP_ID_4623851,Human_RBP_ID_18470895,Human_RBP_ID_19000630,Human_RBP_ID_19102719,Human_RBP_ID_26487617,Human_RBP_ID_26787353 Human_Splice_Rec_358765,Human_Splice_Rec_358777,Human_Splice_Rec_358787,Human_Splice_Rec_358793 RMVar_hsa_circ_96993,RMVar_hsa_circ_268733,RMVar_hsa_circ_98997,RMVar_hsa_circ_206917,RMVar_hsa_circ_206918 84914 RMVar_ID_84914 Human_SNP_ID_113376060 m1A Human chr2 + 218404299 218404299 218404299 CCCCTCATCTTCCTACACCCACTTCCCCAGGTACCGGTGGCCTCGTGGTTTGACAACATGAGTGA CCCCTCATCTTCCTACACCCACTTCCCCAGGTGCCGGTGGCCTCGTGGTTTGACAACATGAGTGA A G CTDSP1 Ensembl:ENSG00000144579 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:218404298..218405046 32194978 MeRIP-seq:(Medium) rs573257676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4596432,Human_RBP_ID_19098703,Human_RBP_ID_23853354 Human_Splice_Rec_358728,Human_Splice_Rec_358740,Human_Splice_Rec_358776,Human_Splice_Rec_358804,Human_Splice_Rec_358816,Human_Splice_Rec_358834,Human_Splice_Rec_358854 RMVar_hsa_circ_96993,RMVar_hsa_circ_206917,RMVar_hsa_circ_120609,RMVar_hsa_circ_206920,RMVar_hsa_circ_115103,RMVar_hsa_circ_112105,RMVar_hsa_circ_125268,RMVar_hsa_circ_206922,RMVar_hsa_circ_206923,RMVar_hsa_circ_206924 84915 RMVar_ID_84915 Human_SNP_ID_113376164 m1A Human chr2 + 218404534 218404534 218404534 GTTAGGAAAACCCATGGGCCGCCGCCACACTCAGTGCCATGGGGAAGCGGGCGTCTCCCCCACCA GTTAGGAAAACCCATGGGCCGCCGCCACACTCGGTGCCATGGGGAAGCGGGCGTCTCCCCCACCA A G CTDSP1 Ensembl:ENSG00000144579 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218404485..218404580 26863196 MeRIP-seq:(Medium) rs562166979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17085533,Human_RBP_ID_20617497 Human_miRNA_ID_2133553,Human_miRNA_ID_2909786 RMVar_hsa_circ_96993,RMVar_hsa_circ_206917,RMVar_hsa_circ_120609,RMVar_hsa_circ_206920,RMVar_hsa_circ_115103,RMVar_hsa_circ_112105,RMVar_hsa_circ_125268,RMVar_hsa_circ_206922,RMVar_hsa_circ_206923,RMVar_hsa_circ_206924 84916 RMVar_ID_84916 Human_SNP_ID_113376551 m1A Human chr2 + 218405573 218405573 218405573 GGACCTTCTGTGGGGTTTGGGGATCTCCAGGAAGCCCGACCAAGCTGTCCCCTTCCCCTGTGCCA GGACCTTCTGTGGGGTTTGGGGATCTCCAGGAGGCCCGACCAAGCTGTCCCCTTCCCCTGTGCCA A G CTDSP1 Ensembl:ENSG00000144579 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:218405526..218405684 26863196 MeRIP-seq:(Medium) rs1559139952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544350,Human_RBP_ID_8201756,Human_RBP_ID_8512357,Human_RBP_ID_17084711 Human_miRNA_ID_869630,Human_miRNA_ID_1200901,Human_miRNA_ID_2579509 RMVar_hsa_circ_96993,RMVar_hsa_circ_206917,RMVar_hsa_circ_120609,RMVar_hsa_circ_206920,RMVar_hsa_circ_115103,RMVar_hsa_circ_112105,RMVar_hsa_circ_125268,RMVar_hsa_circ_206922,RMVar_hsa_circ_206923,RMVar_hsa_circ_206924 84917 RMVar_ID_84917 Human_SNP_ID_113376587 m1A Human chr2 + 218405662 218405662 218405662 TGATCCCCTGCTGGCTGGGGGCAGCTCCCAGGATATCCTGCCTTCCAACTGTTTCTGAAGCCCCT TGATCCCCTGCTGGCTGGGGGCAGCTCCCAGGGTATCCTGCCTTCCAACTGTTTCTGAAGCCCCT A G CTDSP1 Ensembl:ENSG00000144579 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:218405526..218405700 26863196 MeRIP-seq:(Medium) rs1277015388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17084711,Human_RBP_ID_17280071,Human_RBP_ID_24378828 Human_miRNA_ID_254705,Human_miRNA_ID_2038808,Human_miRNA_ID_2931067,Human_miRNA_ID_3017790 RMVar_hsa_circ_96993,RMVar_hsa_circ_206917,RMVar_hsa_circ_120609,RMVar_hsa_circ_206920,RMVar_hsa_circ_115103,RMVar_hsa_circ_112105,RMVar_hsa_circ_125268,RMVar_hsa_circ_206922,RMVar_hsa_circ_206923,RMVar_hsa_circ_206924 84918 RMVar_ID_84918 Human_SNP_ID_113417286 m1A Human chr2 - 218568911 218568901 218568912 CCGCCGCTCTCTTCCACAGCCGGACGCGTCCGACCCGCGTCCCCCCTTCAGCACCCCTGCAGCGG CCGCCGCTCTCTTCCACAGCCGGACGCGTCC___________CCCCTTCAGCACCCCTGCAGCGG GGGACGCGGGTC G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:218568865..218569025 26863196 MeRIP-seq:(Medium) rs1005377278 Functional Loss DEL dbSNP153 32..42 33 - - - 84919 RMVar_ID_84919 Human_SNP_ID_113420246 m1A Human chr2 + 218580646 218580646 218580646 CAATGAGCTGTCCAGTCCTGAGACTAGGGAAAATGCTTTGCTGGAGCTAAGTAAGAAGCGAGAAT CAATGAGCTGTCCAGTCCTGAGACTAGGGAAAGTGCTTTGCTGGAGCTAAGTAAGAAGCGAGAAT A G CNOT9 Ensembl:ENSG00000144580 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218580595..218580750 32194978 MeRIP-seq:(Medium) rs1170015272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1911206,Human_RBP_ID_4623855,Human_RBP_ID_5147219,Human_RBP_ID_13774808,Human_RBP_ID_23853524,Human_RBP_ID_26342225 Human_Splice_Rec_359208,Human_Splice_Rec_359209,Human_Splice_Rec_359224,Human_Splice_Rec_359225,Human_Splice_Rec_359238,Human_Splice_Rec_359239,Human_Splice_Rec_359254,Human_Splice_Rec_359256,Human_Splice_Rec_359257,Human_Splice_Rec_359264,Human_Splice_Rec_359265 Human_miRNA_ID_2430139,Human_miRNA_ID_2530904,Human_miRNA_ID_2881082 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206988,RMVar_hsa_circ_294262,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984,RMVar_hsa_circ_324181,RMVar_hsa_circ_331783,RMVar_hsa_circ_374052,RMVar_hsa_circ_301127,RMVar_hsa_circ_93825,RMVar_hsa_circ_289426,RMVar_hsa_circ_206989,RMVar_hsa_circ_206986,RMVar_hsa_circ_206987,RMVar_hsa_circ_206985 84920 RMVar_ID_84920 Human_SNP_ID_113423901 m1A Human chr2 - 218594885 218594885 218594885 TGATGCAGCTATTGGCCTGCCAGAGGGGATGTAATGCCCAGACCAACTTTTTATTGAGCTTATGC TGATGCAGCTATTGGCCTGCCAGAGGGGATGTGATGCCCAGACCAACTTTTTATTGAGCTTATGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218594834..218594935 32194978 MeRIP-seq:(Medium) rs1386282400 Functional Loss SNV dbSNP153 33..33 33 - - - 84921 RMVar_ID_84921 Human_SNP_ID_113423944 m1A Human chr2 - 218595085 218595081 218595085 AAGTTTAATAGAAGGGAAGTTCAAAAAGGGAAAGCACTGAGATTTGGGAAAACTAGCAGCTAAAG AAGTTTAATAGAAGGGAAGTTCAAAAAGGGAA____CTGAGATTTGGGAAAACTAGCAGCTAAAG GTGCT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218595034..218595234 32194978 MeRIP-seq:(Medium) rs140782358 Functional Loss DEL dbSNP153 33..36 33 - - - 84922 RMVar_ID_84922 Human_SNP_ID_113424234 m1A Human chr2 - 218596180 218596180 218596180 ATGGCCAATGCACCGAAAGATGGAGAGAAGAGAATTTCCCAGGGAGCAAGGCCCTGGGCCTCAGC ATGGCCAATGCACCGAAAGATGGAGAGAAGAGGATTTCCCAGGGAGCAAGGCCCTGGGCCTCAGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218595832..218596182 32194978 MeRIP-seq:(Medium) rs950626694 Functional Loss SNV dbSNP153 33..33 33 - - - 84923 RMVar_ID_84923 Human_SNP_ID_113437176 m1A Human chr2 - 218644483 218644483 218644483 ACAGGAGGGCAGTGAGGCTCCCCATGGGGGTGACCTGGGTGGCAGTCCCAGCCCAGCAGAGGTGG ACAGGAGGGCAGTGAGGCTCCCCATGGGGGTGCCCTGGGTGGCAGTCCCAGCCCAGCAGAGGTGG T G ZNF142 Ensembl:ENSG00000115568 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218644439..218644514 26863196 MeRIP-seq:(Medium) rs1313532280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828877,Human_RBP_ID_5528203,Human_RBP_ID_17950696,Human_RBP_ID_22360171 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_365865,RMVar_hsa_circ_207001 84924 RMVar_ID_84924 Human_SNP_ID_113441156 m1A Human chr2 - 218659745 218659745 218659745 TGGTTTGGGGTAACCCGTCACTCAGCCCTCTCACCGCCGTGACTCTCTGGCCCTCCGTCTCGATG TGGTTTGGGGTAACCCGTCACTCAGCCCTCTCCCCGCCGTGACTCTCTGGCCCTCCGTCTCGATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:218659724..218659942;chr2:218659277..218659955;chr2:218659052..218660539;chr2:218659061..218660191 26863196 MeRIP-seq:(Medium) rs1553595166 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_441 84925 RMVar_ID_84925 Human_SNP_ID_113442196 m1A Human chr2 + 218663245 218663245 218663245 CAGATGTTCCAGAGGTTCTATCCAGGGCAGGCACCTTCCTTAGCTGAGAACTTTGCAGAACATGT CAGATGTTCCAGAGGTTCTATCCAGGGCAGGCGCCTTCCTTAGCTGAGAACTTTGCAGAACATGT A G BCS1L Ensembl:ENSG00000074582 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218663194..218663294 32194978 MeRIP-seq:(Medium) rs199661869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544493,Human_RBP_ID_1022023,Human_RBP_ID_1911285,Human_RBP_ID_3616159,Human_RBP_ID_8512506,Human_RBP_ID_13775538,Human_RBP_ID_17950721,Human_RBP_ID_18443076,Human_RBP_ID_23853628 Human_Splice_Rec_359766 Human_miRNA_ID_2143029,Human_miRNA_ID_2144563,Human_miRNA_ID_2687067 RMVar_hsa_circ_120762,RMVar_hsa_circ_84748,RMVar_hsa_circ_207011,RMVar_hsa_circ_207012 84926 RMVar_ID_84926 Human_SNP_ID_113442559 m1A Human chr2 - 218664356 218664356 218664356 GAGAAGATTCCAGGGACCAGGTCAAATCAGCAAAGGTTGGGCGAAACCCAGAAAGCTATGCTAGA GAGAAGATTCCAGGGACCAGGTCAAATCAGCACAGGTTGGGCGAAACCCAGAAAGCTATGCTAGA T G RNF25 Ensembl:ENSG00000163481 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218664306..218664462 26863196 MeRIP-seq:(Medium) rs1384537403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1377183,Human_RBP_ID_1583574,Human_RBP_ID_5146690 84927 RMVar_ID_84927 Human_SNP_ID_113442833 m1A Human chr2 + 218665227 218665227 218665227 AGATCATACACGAGGGGCTCTCTGCACACTGGACACTGCACACCGACTGCCTTCTAAAAAAGAGA AGATCATACACGAGGGGCTCTCTGCACACTGGGCACTGCACACCGACTGCCTTCTAAAAAAGAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218665151..218665975 32194978 MeRIP-seq:(Medium) rs768365662 Functional Loss SNV dbSNP153 33..33 33 - - - 84928 RMVar_ID_84928 Human_SNP_ID_113493465 m1A Human chr2 + 218865529 218865529 218865529 GTCCAATATTTTCACTTACATGTGAGGGCAGCAAGGTCACAGACAGGCGGTGAGAAGATGACTTG GTCCAATATTTTCACTTACATGTGAGGGCAGCGAGGTCACAGACAGGCGGTGAGAAGATGACTTG A G WNT6 Ensembl:ENSG00000115596 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:218865525..218865648 26863196 MeRIP-seq:(Medium) rs1227275443 Functional Loss SNV dbSNP153 33..33 33 - - - 84929 RMVar_ID_84929 Human_SNP_ID_113493684 m1A Human chr2 + 218866386 218866386 218866386 AAGAGGAGGGTCCTAGAGGGTGCATTTGGTCCAGGAGCAGGGCTGGATGGAGGAGGAGGAGACAC AAGAGGAGGGTCCTAGAGGGTGCATTTGGTCCTGGAGCAGGGCTGGATGGAGGAGGAGGAGACAC A T WNT6 Ensembl:ENSG00000115596 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:218866384..218866532 26863196 MeRIP-seq:(Medium) rs948428233 Functional Loss SNV dbSNP153 33..33 33 - - - 84930 RMVar_ID_84930 Human_SNP_ID_113494759 m1A Human chr2 - 218871106 218871106 218871106 CTCTGCCACCACTTCCGGCTCAGCCTGGCACAACTCGGCCTGCCGCCCGGCCAGCCGCCGTGCCT CTCTGCCACCACTTCCGGCTCAGCCTGGCACAGCTCGGCCTGCCGCCCGGCCAGCCGCCGTGCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218871010..218871197 26863196 MeRIP-seq:(Medium) rs201848970 Functional Loss SNV dbSNP153 33..33 33 - - - 84931 RMVar_ID_84931 Human_SNP_ID_113495023 m1A Human chr2 + 218871725 218871725 218871725 AGGCTGCGGCGACGACGTGGACTTCGGGGACGAGAAGTCGAGGCTCTTTATGGACGCGCGGCACA AGGCTGCGGCGACGACGTGGACTTCGGGGACGGGAAGTCGAGGCTCTTTATGGACGCGCGGCACA A G WNT6 Ensembl:ENSG00000115596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:218871701..218871725 26863196 MeRIP-seq:(Medium) rs1487121889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_360537 84932 RMVar_ID_84932 Human_SNP_ID_113495188 m1A Human chr2 - 218872184 218872183 218872184 TGTTTTATTCTCCTGCCCCTGCCTAGGCATCCAGACCTCCTACCCACTGCAAGCTTTGCTTCACC TGTTTTATTCTCCTGCCCCTGCCTAGGCATCC_GACCTCCTACCCACTGCAAGCTTTGCTTCACC CT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:218871992..218872308 26863196 MeRIP-seq:(Medium) rs1193220934 Functional Loss DEL dbSNP153 33..33 33 - - - 84933 RMVar_ID_84933 Human_SNP_ID_113495189 m1A Human chr2 - 218872184 218872184 218872184 TGTTTTATTCTCCTGCCCCTGCCTAGGCATCCAGACCTCCTACCCACTGCAAGCTTTGCTTCACC TGTTTTATTCTCCTGCCCCTGCCTAGGCATCCGGACCTCCTACCCACTGCAAGCTTTGCTTCACC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:218871992..218872308 26863196 MeRIP-seq:(Medium) rs551190254 Functional Loss SNV dbSNP153 33..33 33 - - - 84934 RMVar_ID_84934 Human_SNP_ID_113495548 m1A Human chr2 + 218873434 218873434 218873434 CGCACCGAGTGCAAATGCCACGGGCTGTCGGGATCATGCGCGCTGCGCACCTGCTGGCAGAAGCT CGCACCGAGTGCAAATGCCACGGGCTGTCGGGTTCATGCGCGCTGCGCACCTGCTGGCAGAAGCT A T WNT6 Ensembl:ENSG00000115596 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218873359..218873495 26863196 MeRIP-seq:(Medium) rs1365829285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_360538 84935 RMVar_ID_84935 Human_SNP_ID_113495644 m1A Human chr2 + 218873637 218873637 218873637 CGCCGCCGATTCGCCCGACTTCTGCGCCCCCAACCGACGCACCGGCTCCCCCGGCACGCGCGGTC CGCCGCCGATTCGCCCGACTTCTGCGCCCCCACCCGACGCACCGGCTCCCCCGGCACGCGCGGTC A C WNT6 Ensembl:ENSG00000115596 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218873587..218873701 26863196 MeRIP-seq:(Medium) rs778620463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544531,Human_RBP_ID_27477779 84936 RMVar_ID_84936 Human_SNP_ID_113495645 m1A Human chr2 + 218873637 218873637 218873637 CGCCGCCGATTCGCCCGACTTCTGCGCCCCCAACCGACGCACCGGCTCCCCCGGCACGCGCGGTC CGCCGCCGATTCGCCCGACTTCTGCGCCCCCAGCCGACGCACCGGCTCCCCCGGCACGCGCGGTC A G WNT6 Ensembl:ENSG00000115596 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:218873587..218873701 26863196 MeRIP-seq:(Medium) rs778620463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544531,Human_RBP_ID_27477779 84937 RMVar_ID_84937 Human_SNP_ID_113501049 m1A Human chr2 - 218894223 218894223 218894223 CACACGATGTGACCTTTGCCCACCCTCTGAACACCTCTCCTGCTAGTCTGTCCCTTGATTTCTTC CACACGATGTGACCTTTGCCCACCCTCTGAACGCCTCTCCTGCTAGTCTGTCCCTTGATTTCTTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:218894173..218894297 26863196 MeRIP-seq:(Medium) rs1416641529 Functional Loss SNV dbSNP153 33..33 33 - - - 84938 RMVar_ID_84938 Human_SNP_ID_113571671 m1A Human chr2 - 219176886 219176886 219176886 CAGGTGGACAGGCGGGCAAGGACAGCTCCGCGAGCCCCCTACAACTCGTTTCCTTCCGTTCACCT CAGGTGGACAGGCGGGCAAGGACAGCTCCGCGGGCCCCCTACAACTCGTTTCCTTCCGTTCACCT T C CNPPD1 Ensembl:ENSG00000115649 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:219176814..219176911 26863410 MeRIP-seq:(Medium) rs1025811320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830360,Human_RBP_ID_4622889,Human_RBP_ID_5147704,Human_RBP_ID_22668168 RMVar_hsa_circ_110115,RMVar_hsa_circ_105828,RMVar_hsa_circ_207057,RMVar_hsa_circ_207056 84939 RMVar_ID_84939 Human_SNP_ID_113572354 m1A Human chr2 - 219178391 219178391 219178391 AGGCCCAGGCTCAGGCCCATCCCCGGCCCCCCACCCGCGCCAGTGTTACCCCCGCCACCGCCGCT AGGCCCAGGCTCAGGCCCATCCCCGGCCCCCCCCCCGCGCCAGTGTTACCCCCGCCACCGCCGCT T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:219178297..219178431 26863410 MeRIP-seq:(Medium) rs1242941894 Functional Loss SNV dbSNP153 33..33 33 - - - 84940 RMVar_ID_84940 Human_SNP_ID_113572386 m1A Human chr2 + 219178446 219178446 219178446 GCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCATGAGTGAGGCCACCAGTGAGGCAGAGGAGGAG GCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCCTGAGTGAGGCCACCAGTGAGGCAGAGGAGGAG A C RETREG2 Ensembl:ENSG00000144567 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr2:219178342..219178541;chr2:219178312..219178556 26863196 MeRIP-seq:(Medium) rs1411755610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544565,Human_RBP_ID_778251,Human_RBP_ID_4622891,Human_RBP_ID_5322288,Human_RBP_ID_5378949,Human_RBP_ID_8942623,Human_RBP_ID_9331285,Human_RBP_ID_9353831,Human_RBP_ID_22450085,Human_RBP_ID_26341747,Human_RBP_ID_26770435 84941 RMVar_ID_84941 Human_SNP_ID_113572387 m1A Human chr2 + 219178446 219178446 219178446 GCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCATGAGTGAGGCCACCAGTGAGGCAGAGGAGGAG GCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCTTGAGTGAGGCCACCAGTGAGGCAGAGGAGGAG A T RETREG2 Ensembl:ENSG00000144567 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr2:219178342..219178541;chr2:219178312..219178556 26863196 MeRIP-seq:(Medium) rs1411755610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544565,Human_RBP_ID_778251,Human_RBP_ID_4622891,Human_RBP_ID_5322288,Human_RBP_ID_5378949,Human_RBP_ID_8942623,Human_RBP_ID_9331285,Human_RBP_ID_9353831,Human_RBP_ID_22450085,Human_RBP_ID_26341747,Human_RBP_ID_26770435 84942 RMVar_ID_84942 Human_SNP_ID_113573856 m1A Human chr2 - 219182522 219182522 219182522 ATCAGGGGGTTTTGGCGGTGTCTCTGGCTCCAAGCCCAGCTCTGCATTCAGCTGCTCCAGCTCCC ATCAGGGGGTTTTGGCGGTGTCTCTGGCTCCATGCCCAGCTCTGCATTCAGCTGCTCCAGCTCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219182472..219182604 26863196 MeRIP-seq:(Medium) rs1197573713 Functional Loss SNV dbSNP153 33..33 33 - - - 84943 RMVar_ID_84943 Human_SNP_ID_113574051 m1A Human chr2 - 219183081 219183081 219183081 GTTGAGCTGCTAAGGACAGGACACAGCAGGGAAATAAAGCAGAAAGGAACACAAGACAAGAGAAA GTTGAGCTGCTAAGGACAGGACACAGCAGGGAGATAAAGCAGAAAGGAACACAAGACAAGAGAAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219183033..219183234 32194978 MeRIP-seq:(Medium) rs1139922 Functional Loss SNV dbSNP153 33..33 33 - - - 84944 RMVar_ID_84944 Human_SNP_ID_113574151 m1A Human chr2 + 219183446 219183446 219183446 CCCCCTACTAGGGTCAGGAAGTGGACACTAACATCTGTGCAGGTGTTGACTTGAAAAATAAAGTG CCCCCTACTAGGGTCAGGAAGTGGACACTAACGTCTGTGCAGGTGTTGACTTGAAAAATAAAGTG A G RETREG2 Ensembl:ENSG00000144567 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:219183183..219183500 32194978 MeRIP-seq:(Medium) rs1479727456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544606,Human_RBP_ID_1583600,Human_RBP_ID_17965760,Human_RBP_ID_20530735,Human_RBP_ID_23853892 84945 RMVar_ID_84945 Human_SNP_ID_113581459 m1A Human chr2 - 219208350 219208350 219208350 GAAAAAGGGGGAGCAGGGAAACGGGCAGGCCTACCTGCTGGGAGAGGTACAGGAAGGCATGGTTT GAAAAAGGGGGAGCAGGGAAACGGGCAGGCCTGCCTGCTGGGAGAGGTACAGGAAGGCATGGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219208338..219208403 26863196 MeRIP-seq:(Medium) rs1411586033 Functional Loss SNV dbSNP153 33..33 33 - - - 84946 RMVar_ID_84946 Human_SNP_ID_113581681 m1A Human chr2 + 219208992 219208992 219208992 CTGTTTCTCCCTCCCAGTTGTCAGGAGGAAGAAGACCTAGCTTTAGCACAAGCACTGTCAGCCAG CTGTTTCTCCCTCCCAGTTGTCAGGAGGAAGACGACCTAGCTTTAGCACAAGCACTGTCAGCCAG A C ZFAND2B Ensembl:ENSG00000158552 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219208976..219209102 32194978 MeRIP-seq:(Medium) rs760888970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1911357,Human_RBP_ID_3616300,Human_RBP_ID_18167311,Human_RBP_ID_22248025,Human_RBP_ID_25578933 Human_Splice_Rec_361330,Human_Splice_Rec_361331,Human_Splice_Rec_361358,Human_Splice_Rec_361359,Human_Splice_Rec_361374,Human_Splice_Rec_361375,Human_Splice_Rec_361436,Human_Splice_Rec_361437,Human_Splice_Rec_361514,Human_Splice_Rec_361515 RMVar_hsa_circ_100093,RMVar_hsa_circ_367776,RMVar_hsa_circ_207068,RMVar_hsa_circ_118842,RMVar_hsa_circ_207071 84947 RMVar_ID_84947 Human_SNP_ID_113581682 m1A Human chr2 + 219208992 219208992 219208992 CTGTTTCTCCCTCCCAGTTGTCAGGAGGAAGAAGACCTAGCTTTAGCACAAGCACTGTCAGCCAG CTGTTTCTCCCTCCCAGTTGTCAGGAGGAAGAGGACCTAGCTTTAGCACAAGCACTGTCAGCCAG A G ZFAND2B Ensembl:ENSG00000158552 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219208976..219209102 32194978 MeRIP-seq:(Medium) rs760888970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1911357,Human_RBP_ID_3616300,Human_RBP_ID_18167311,Human_RBP_ID_22248025,Human_RBP_ID_25578933 Human_Splice_Rec_361330,Human_Splice_Rec_361331,Human_Splice_Rec_361358,Human_Splice_Rec_361359,Human_Splice_Rec_361374,Human_Splice_Rec_361375,Human_Splice_Rec_361436,Human_Splice_Rec_361437,Human_Splice_Rec_361514,Human_Splice_Rec_361515 RMVar_hsa_circ_100093,RMVar_hsa_circ_367776,RMVar_hsa_circ_207068,RMVar_hsa_circ_118842,RMVar_hsa_circ_207071 84948 RMVar_ID_84948 Human_SNP_ID_113581822 m1A Human chr2 + 219209390 219209390 219209390 ACCTCTAGGGTACACAGGGAGAGGAGGCCCGGAGCACCCTGGAGGGCAGAGACAAGCGGGAGTGA ACCTCTAGGGTACACAGGGAGAGGAGGCCCGGGGCACCCTGGAGGGCAGAGACAAGCGGGAGTGA A G ZFAND2B Ensembl:ENSG00000158552 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219209251..219209625 32194978 MeRIP-seq:(Medium) rs1282991518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9430286,Human_RBP_ID_18167313,Human_RBP_ID_26786644 RMVar_hsa_circ_100093,RMVar_hsa_circ_207068 84949 RMVar_ID_84949 Human_SNP_ID_113585202 m1A Human chr2 + 219218899 219218899 219218899 CACGCACTCACGCAGGGCACGTACGCCGTCTCAGCACGGCCCCGCTGGCTCTGGGCCCGGGACCC CACGCACTCACGCAGGGCACGTACGCCGTCTCTGCACGGCCCCGCTGGCTCTGGGCCCGGGACCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219218710..219218950 26863196 MeRIP-seq:(Medium) rs1323879320 Functional Loss SNV dbSNP153 33..33 33 - - - 84950 RMVar_ID_84950 Human_SNP_ID_113585891 m1A Human chr2 + 219220880 219220880 219220880 GCAGCCGAGAGAAATGAGAGGGAACCCTGGGCACTGTGCCAGGATCTGGAGAGACAAGTAAGAGT GCAGCCGAGAGAAATGAGAGGGAACCCTGGGCCCTGTGCCAGGATCTGGAGAGACAAGTAAGAGT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:219220726..219220900 26863196 MeRIP-seq:(Medium) rs749288489 Functional Loss SNV dbSNP153 33..33 33 - - - 84951 RMVar_ID_84951 Human_SNP_ID_113586571 m1A Human chr2 - 219222726 219222726 219222726 TTCCTCAAGGAGCAGGTTCAGCGGGATGGAGCAGCTGCTAGCCTCGCCCAAGGGGGTCTGCTCCC TTCCTCAAGGAGCAGGTTCAGCGGGATGGAGCGGCTGCTAGCCTCGCCCAAGGGGGTCTGCTCCC T C AC068946.2,ATG9A Ensembl:ENSG00000284820,Ensembl:ENSG00000198925 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219222676..219222750 32194978 MeRIP-seq:(Medium) rs1312866876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17279357 Human_Splice_Rec_361689,Human_Splice_Rec_361749,Human_Splice_Rec_361777,Human_Splice_Rec_361803,Human_Splice_Rec_361831,Human_Splice_Rec_361861,Human_Splice_Rec_361875 Human_miRNA_ID_2649193,Human_miRNA_ID_2651140 RMVar_hsa_circ_22301,RMVar_hsa_circ_82742,RMVar_hsa_circ_207084,RMVar_hsa_circ_79724,RMVar_hsa_circ_43229,RMVar_hsa_circ_207085 84952 RMVar_ID_84952 Human_SNP_ID_113588600 m1A Human chr2 - 219229582 219229573 219229582 CGCCGCGGGTCGCGCCGAGCCGAGCCGAGCCGAGCGGAGCCGGCGGAGCCTCTGGAATCACCCGG CGCCGCGGGTCGCGCCGAGCCGAGCCGAGCCG_________GGCGGAGCCTCTGGAATCACCCGG CGGCTCCGCT C ATG9A Ensembl:ENSG00000198925 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219229365..219229586 26863196 MeRIP-seq:(Medium) rs1452709505 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4623870 Human_Splice_Rec_361731,Human_Splice_Rec_361759,Human_Splice_Rec_361787,Human_Splice_Rec_361847,Human_Splice_Rec_361879,Human_Splice_Rec_361885,Human_Splice_Rec_361899,Human_Splice_Rec_361909,Human_Splice_Rec_361919,Human_Splice_Rec_361935,Human_Splice_Rec_361945,Human_Splice_Rec_361955,Human_Splice_Rec_361963,Human_Splice_Rec_361967 84953 RMVar_ID_84953 Human_SNP_ID_113588611 m1A Human chr2 - 219229582 219229582 219229582 CGCCGCGGGTCGCGCCGAGCCGAGCCGAGCCGAGCGGAGCCGGCGGAGCCTCTGGAATCACCCGG CGCCGCGGGTCGCGCCGAGCCGAGCCGAGCCGGGCGGAGCCGGCGGAGCCTCTGGAATCACCCGG T C ATG9A Ensembl:ENSG00000198925 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219229365..219229586 26863196 MeRIP-seq:(Medium) rs917911692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623870 Human_Splice_Rec_361731,Human_Splice_Rec_361759,Human_Splice_Rec_361787,Human_Splice_Rec_361847,Human_Splice_Rec_361879,Human_Splice_Rec_361885,Human_Splice_Rec_361899,Human_Splice_Rec_361909,Human_Splice_Rec_361919,Human_Splice_Rec_361935,Human_Splice_Rec_361945,Human_Splice_Rec_361955,Human_Splice_Rec_361963,Human_Splice_Rec_361967 84954 RMVar_ID_84954 Human_SNP_ID_113588742 m1A Human chr2 - 219229898 219229898 219229898 TAAACTCGCCCACGCCCTTAGAAGACGCACCAAACGTCCCGGGAGCTGAGCGGCTCGCAAGTCCT TAAACTCGCCCACGCCCTTAGAAGACGCACCAGACGTCCCGGGAGCTGAGCGGCTCGCAAGTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219229863..219229939 26863196 MeRIP-seq:(Medium) rs1387452952 Functional Loss SNV dbSNP153 33..33 33 - - - 84955 RMVar_ID_84955 Human_SNP_ID_113589834 m1A Human chr2 - 219233373 219233373 219233373 CTCAGGTTGGCTCCAGCAGAGTGTGATGGCCCACCTCGGGCATCCCGAAGCCCCTGGGCTGTGCC CTCAGGTTGGCTCCAGCAGAGTGTGATGGCCCCCCTCGGGCATCCCGAAGCCCCTGGGCTGTGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219233326..219233425 32194978 MeRIP-seq:(Medium) rs745362383 Functional Loss SNV dbSNP153 33..33 33 - - - 84956 RMVar_ID_84956 Human_SNP_ID_113590348 m1A Human chr2 + 219234924 219234924 219234924 CTCTGGATCTTTGTGAGTCTGAAGTATTGCCCAAGCGGAGGAGGAGAAAAAGGAATAAGAAGGAG CTCTGGATCTTTGTGAGTCTGAAGTATTGCCCGAGCGGAGGAGGAGAAAAAGGAATAAGAAGGAG A G ANKZF1 Ensembl:ENSG00000163516 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:219234808..219235025;chr2:219234780..219234952 26863196 MeRIP-seq:(Medium) rs1413476202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919327,Human_RBP_ID_2623562,Human_RBP_ID_3958499,Human_RBP_ID_18470921,Human_RBP_ID_19003132,Human_RBP_ID_22076843,Human_RBP_ID_22417267,Human_RBP_ID_23119346,Human_RBP_ID_23853980,Human_RBP_ID_26341755 Human_Splice_Rec_362010,Human_Splice_Rec_362060,Human_Splice_Rec_362148 RMVar_hsa_circ_8897 84957 RMVar_ID_84957 Human_SNP_ID_113590641 m1A Human chr2 + 219235642 219235642 219235642 CAGAGTGGGAAGGCATCACAGATCCTGGCTAGATCCTTTCTACTTCTTGCAGTTTTACCAAAGAT CAGAGTGGGAAGGCATCACAGATCCTGGCTAGGTCCTTTCTACTTCTTGCAGTTTTACCAAAGAT A G ANKZF1 Ensembl:ENSG00000163516 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:219235639..219235739 32194978 MeRIP-seq:(Medium) rs1295053784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22417276,Human_RBP_ID_22547840,Human_RBP_ID_22670458,Human_RBP_ID_25515549 RMVar_hsa_circ_8897 84958 RMVar_ID_84958 Human_SNP_ID_113590691 m1A Human chr2 + 219235768 219235768 219235768 AGGCACGGCAGGCTACACGGAAAAGGGAGCAGAAGGCAGCCCGGCGGCAACGGGAGGAACAGCAG AGGCACGGCAGGCTACACGGAAAAGGGAGCAGGAGGCAGCCCGGCGGCAACGGGAGGAACAGCAG A G ANKZF1 Ensembl:ENSG00000163516 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219235717..219235826 26863196 MeRIP-seq:(Medium) rs938592227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919334,Human_RBP_ID_3958500,Human_RBP_ID_9388018,Human_RBP_ID_19003136,Human_RBP_ID_24545939,Human_RBP_ID_27818002 Human_Splice_Rec_362014,Human_Splice_Rec_362064,Human_Splice_Rec_362086,Human_Splice_Rec_362152,Human_Splice_Rec_362198 RMVar_hsa_circ_8897 84959 RMVar_ID_84959 Human_SNP_ID_113590692 m1A Human chr2 + 219235768 219235768 219235768 AGGCACGGCAGGCTACACGGAAAAGGGAGCAGAAGGCAGCCCGGCGGCAACGGGAGGAACAGCAG AGGCACGGCAGGCTACACGGAAAAGGGAGCAGTAGGCAGCCCGGCGGCAACGGGAGGAACAGCAG A T ANKZF1 Ensembl:ENSG00000163516 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219235717..219235826 26863196 MeRIP-seq:(Medium) rs938592227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919334,Human_RBP_ID_3958500,Human_RBP_ID_9388018,Human_RBP_ID_19003136,Human_RBP_ID_24545939,Human_RBP_ID_27818002 Human_Splice_Rec_362014,Human_Splice_Rec_362064,Human_Splice_Rec_362086,Human_Splice_Rec_362152,Human_Splice_Rec_362198 RMVar_hsa_circ_8897 84960 RMVar_ID_84960 Human_SNP_ID_113590748 m1A Human chr2 + 219235861 219235861 219235861 AACGAGAAGAGCAGCGGCGATTTGCCGCCCTCAGTGACCGAGAGAAGGTGAGGCTGGAGGTTCTC AACGAGAAGAGCAGCGGCGATTTGCCGCCCTCGGTGACCGAGAGAAGGTGAGGCTGGAGGTTCTC A G ANKZF1 Ensembl:ENSG00000163516 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219235688..219236072 32194978 MeRIP-seq:(Medium) rs771456010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_916832,Human_RBP_ID_3958501,Human_RBP_ID_9388019,Human_RBP_ID_18470923,Human_RBP_ID_19003137,Human_RBP_ID_26340298 Human_Splice_Rec_362015,Human_Splice_Rec_362065,Human_Splice_Rec_362087,Human_Splice_Rec_362119,Human_Splice_Rec_362153,Human_Splice_Rec_362199 RMVar_hsa_circ_8897 84961 RMVar_ID_84961 Human_SNP_ID_113595497 m1A Human chr2 + 219250805 219250805 219250805 TGCCGGGGATCACACTTTACCATCTGGTTGGCAGGCTCAAAGCAGGCATTGGTGATCTCTGCCAC TGCCGGGGATCACACTTTACCATCTGGTTGGCCGGCTCAAAGCAGGCATTGGTGATCTCTGCCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219250754..219250822 26863196 MeRIP-seq:(Medium) rs1559276075 Functional Loss SNV dbSNP153 33..33 33 - - - 84962 RMVar_ID_84962 Human_SNP_ID_113602567 m1A Human chr2 + 219279430 219279430 219279430 CGCACAGCTGGGCCGGGCGCGTCCTACGCAGCAGCCGCGAGCCGGGCTGCGGGTGCCAGACGGTT CGCACAGCTGGGCCGGGCGCGTCCTACGCAGCCGCCGCGAGCCGGGCTGCGGGTGCCAGACGGTT A C DNAJB2 Ensembl:ENSG00000135924 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219279380..219279567 26863196 MeRIP-seq:(Medium) rs1020887628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625123,Human_RBP_ID_18422488 Human_Splice_Rec_362537,Human_Splice_Rec_362553,Human_Splice_Rec_362569,Human_Splice_Rec_362587,Human_Splice_Rec_362595,Human_Splice_Rec_362603,Human_Splice_Rec_362613,Human_Splice_Rec_362615 84963 RMVar_ID_84963 Human_SNP_ID_113602600 m1A Human chr2 - 219279520 219279520 219279520 GGGCCCCCAGCCTGACCCGGGCCCCCGGCCGCACCTCCTCCGCCAGGAGTCCCGGCCTCCTGCGG GGGCCCCCAGCCTGACCCGGGCCCCCGGCCGCCCCTCCTCCGCCAGGAGTCCCGGCCTCCTGCGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219279416..219279566 32194978 MeRIP-seq:(Medium) rs952854988 Functional Loss SNV dbSNP153 33..33 33 - - - 84964 RMVar_ID_84964 Human_SNP_ID_113602696 m1A Human chr2 + 219279806 219279806 219279806 CGCCTGACTCCTTCTCTTCTGCAGCCCCAAGGAGGCCCGCCTGACGACTGACCAGTTGCCATGGC CGCCTGACTCCTTCTCTTCTGCAGCCCCAAGGCGGCCCGCCTGACGACTGACCAGTTGCCATGGC A C DNAJB2 Ensembl:ENSG00000135924 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219279366..219279915 26863196 MeRIP-seq:(Medium) rs1188760272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4597355,Human_RBP_ID_22670461,Human_RBP_ID_22743077 Human_Splice_Rec_362538,Human_Splice_Rec_362539,Human_Splice_Rec_362554,Human_Splice_Rec_362555,Human_Splice_Rec_362570,Human_Splice_Rec_362571,Human_Splice_Rec_362588,Human_Splice_Rec_362589,Human_Splice_Rec_362596,Human_Splice_Rec_362597,Human_Splice_Rec_362604,Human_Splice_Rec_362605,Human_Splice_Rec_362614,Human_Splice_Rec_362616,Human_Splice_Rec_362617,Human_Splice_Rec_362629,Human_Splice_Rec_362638,Human_Splice_Rec_362639,Human_Splice_Rec_362647 RMVar_hsa_circ_445,RMVar_hsa_circ_2732 84965 RMVar_ID_84965 Human_SNP_ID_113603230 m1A Human chr2 + 219281724 219281724 219281724 TGAAATGATCTGGTCTCTTTTTGCAGAGCACAAGCGGGAGATTTACGACCGCTATGGCCGGGAAG TGAAATGATCTGGTCTCTTTTTGCAGAGCACAGGCGGGAGATTTACGACCGCTATGGCCGGGAAG A G DNAJB2 Ensembl:ENSG00000135924 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219281701..219281725 26863196 MeRIP-seq:(Medium) rs778291801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19003145 Human_Splice_Rec_362542,Human_Splice_Rec_362543,Human_Splice_Rec_362558,Human_Splice_Rec_362559,Human_Splice_Rec_362574,Human_Splice_Rec_362575,Human_Splice_Rec_362592,Human_Splice_Rec_362593,Human_Splice_Rec_362600,Human_Splice_Rec_362601,Human_Splice_Rec_362607,Human_Splice_Rec_362620,Human_Splice_Rec_362621,Human_Splice_Rec_362632,Human_Splice_Rec_362633,Human_Splice_Rec_362642,Human_Splice_Rec_362643,Human_Splice_Rec_362654,Human_Splice_Rec_362655,Human_Splice_Rec_362666,Human_Splice_Rec_362667 RMVar_hsa_circ_2732,RMVar_hsa_circ_2964 84966 RMVar_ID_84966 Human_SNP_ID_113603817 m1A Human chr2 - 219283474 219283472 219283475 GGGGAGCTGCTCCTCACCATTGATTGTGACTGACTTCAGCTGCCCATCCTCCTCCACTTCCACCC GGGGAGCTGCTCCTCACCATTGATTGTGACT___TTCAGCTGCCCATCCTCCTCCACTTCCACCC AGTC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:219283363..219284775;chr2:219283384..219284947 26863196 MeRIP-seq:(Medium) rs762959655 Functional Loss DEL dbSNP153 32..34 33 - - - 84967 RMVar_ID_84967 Human_SNP_ID_113604466 m1A Human chr2 + 219285687 219285687 219285687 ATCTTCTGGGGAGGCTAGCCGGGTGGGGCGGGAGCCTCTCAGCTGTCCAGATTCAGAACTGGAGC ATCTTCTGGGGAGGCTAGCCGGGTGGGGCGGGGGCCTCTCAGCTGTCCAGATTCAGAACTGGAGC A G DNAJB2 Ensembl:ENSG00000135924 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219285649..219285755 26863196 MeRIP-seq:(Medium) rs914316370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21980882 Human_Splice_Rec_362689 84968 RMVar_ID_84968 Human_SNP_ID_113629255 m1A Human chr2 + 219374963 219374963 219374963 CTGCCTAAATCCAGCACCCGCAGCCCCAGCCGAGAAGCCAAGATAGGTCCAATGGTGGTTCCACA CTGCCTAAATCCAGCACCCGCAGCCCCAGCCGGGAAGCCAAGATAGGTCCAATGGTGGTTCCACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:219374854..219375005 32194978 MeRIP-seq:(Medium) rs772183526 Functional Loss SNV dbSNP153 33..33 33 - - - 84969 RMVar_ID_84969 Human_SNP_ID_113632294 m1A Human chr2 + 219386058 219386058 219386058 CCAGGTGTGGGATGCGAAGAATGGGCCGCTCCACGTGCACCAGCTGCTGCTCCAGCCGACCTGAG CCAGGTGTGGGATGCGAAGAATGGGCCGCTCCGCGTGCACCAGCTGCTGCTCCAGCCGACCTGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:219385831..219386064 32194978 MeRIP-seq:(Medium) rs1459757180 Functional Loss SNV dbSNP153 33..33 33 - - - 84970 RMVar_ID_84970 Human_SNP_ID_113632980 m1A Human chr2 + 219387821 219387821 219387821 GCTCATCTGGCCTCCGGGCTCGGCCCGCCCCCACCGCGCCGCCTGCCCCGCCCCTCACTAGCTTT GCTCATCTGGCCTCCGGGCTCGGCCCGCCCCCCCCGCGCCGCCTGCCCCGCCCCTCACTAGCTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219387602..219387925 26863196 MeRIP-seq:(Medium) rs933057081 Functional Loss SNV dbSNP153 33..33 33 - - - 84971 RMVar_ID_84971 Human_SNP_ID_113632997 m1A Human chr2 + 219387856 219387855 219387856 GCGCCGCCTGCCCCGCCCCTCACTAGCTTTGCAGGTCCCCCGCGTGCCCCTTCAGGCCGCGCCGC GCGCCGCCTGCCCCGCCCCTCACTAGCTTTGC_GGTCCCCCGCGTGCCCCTTCAGGCCGCGCCGC CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219387704..219387908 26863196 MeRIP-seq:(Medium) rs1232036253 Functional Loss DEL dbSNP153 33..33 33 - - - 84972 RMVar_ID_84972 Human_SNP_ID_113646465 m1A Human chr2 + 219443140 219443140 219443140 AAAACCGGCCATTCCCGCCGGGCCTTTGGCCGACTCACCCATGGTGCGTGGACCGTGGGCGTCCT AAAACCGGCCATTCCCGCCGGGCCTTTGGCCGGCTCACCCATGGTGCGTGGACCGTGGGCGTCCT A G SPEG Ensembl:ENSG00000072195 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219443132..219443317 26863196 MeRIP-seq:(Medium) rs779189448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26340304 Human_Splice_Rec_363432,Human_Splice_Rec_363452,Human_Splice_Rec_363453,Human_Splice_Rec_363460,Human_Splice_Rec_363468,Human_Splice_Rec_363469,Human_Splice_Rec_363476,Human_Splice_Rec_363477,Human_Splice_Rec_363496,Human_Splice_Rec_363497,Human_Splice_Rec_363504 84973 RMVar_ID_84973 Human_SNP_ID_113647191 m1A Human chr2 - 219445812 219445812 219445812 ATGAGAGAAATCATTGCAAGCCCCCTGCCACCATCACTCCCGCCCTCTCCCTCTGGCCTGGCCCC ATGAGAGAAATCATTGCAAGCCCCCTGCCACCGTCACTCCCGCCCTCTCCCTCTGGCCTGGCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219445810..219446167 26863196 MeRIP-seq:(Medium) rs1228450819 Functional Loss SNV dbSNP153 33..33 33 - - - 84974 RMVar_ID_84974 Human_SNP_ID_113647221 m1A Human chr2 + 219445941 219445941 219445941 AGGTGTTGGAGGCACTGGAGCCATTTTTGGAGATTTGGGGCTCGCAGATACAGGAGGGAGTGCTA AGGTGTTGGAGGCACTGGAGCCATTTTTGGAGGTTTGGGGCTCGCAGATACAGGAGGGAGTGCTA A G SPEG Ensembl:ENSG00000072195 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:219445892..219446098 26863196 MeRIP-seq:(Medium) rs1161973153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207103,RMVar_hsa_circ_111047 84975 RMVar_ID_84975 Human_SNP_ID_113647834 m1A Human chr2 + 219448138 219448138 219448138 CGGGAAGCGGTCCCCGCCGGGACCCCCGGCCCAGCCCGCGGCCACCCCCACGTCGCCCCACCGTC CGGGAAGCGGTCCCCGCCGGGACCCCCGGCCCCGCCCGCGGCCACCCCCACGTCGCCCCACCGTC A C SPEG Ensembl:ENSG00000072195 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219448092..219448180 26863196 MeRIP-seq:(Medium) rs1445263629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207103,RMVar_hsa_circ_111047,RMVar_hsa_circ_336806,RMVar_hsa_circ_377962 84976 RMVar_ID_84976 Human_SNP_ID_113648133 m1A Human chr2 + 219448846 219448846 219448846 CGCCCAGCCGCCCTCTCCGAGCAGCGCGGAGAAGCCGGGGGACGAGCCTGGGAGGCCCAGGAGCC CGCCCAGCCGCCCTCTCCGAGCAGCGCGGAGAGGCCGGGGGACGAGCCTGGGAGGCCCAGGAGCC A G SPEG Ensembl:ENSG00000072195 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219448801..219449111 26863196 MeRIP-seq:(Medium) rs1454784472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207103,RMVar_hsa_circ_111047,RMVar_hsa_circ_336806,RMVar_hsa_circ_377962 84977 RMVar_ID_84977 Human_SNP_ID_113652899 m1A Human chr2 + 219466386 219466386 219466386 TCTCTCCCTGAAGGGGAGCACCGGGCGAGTGCATGTGCTACTGCTGCTACAGGCCTGTCTATCTG TCTCTCCCTGAAGGGGAGCACCGGGCGAGTGCGTGTGCTACTGCTGCTACAGGCCTGTCTATCTG A G SPEG Ensembl:ENSG00000072195 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219466026..219466426 32194978 MeRIP-seq:(Medium) rs1207121143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544740,Human_RBP_ID_23854097 RMVar_hsa_circ_207103,RMVar_hsa_circ_111047,RMVar_hsa_circ_121599,RMVar_hsa_circ_92943,RMVar_hsa_circ_207105,RMVar_hsa_circ_207106,RMVar_hsa_circ_100655,RMVar_hsa_circ_207109 84978 RMVar_ID_84978 Human_SNP_ID_113657480 m1A Human chr2 - 219482833 219482833 219482833 CTGCCACACTTACCTGCCACCTCCGCCGGGAGAGGAATAGCTTCAGGTGATCCGTGCTCACCTCT CTGCCACACTTACCTGCCACCTCCGCCGGGAGTGGAATAGCTTCAGGTGATCCGTGCTCACCTCT T A ASIC4-AS1 Ensembl:ENSG00000227432 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219482824..219483170 32194978 MeRIP-seq:(Medium) rs1401743049 Functional Loss SNV dbSNP153 33..33 33 - - - 84979 RMVar_ID_84979 Human_SNP_ID_113657681 m1A Human chr2 + 219483314 219483314 219483314 AGCCCGAGTTCTCTGGCTCCCGGGTGTCCCTCACAGACATTCCCACTGAGGATGAGGCCCTGGGG AGCCCGAGTTCTCTGGCTCCCGGGTGTCCCTCCCAGACATTCCCACTGAGGATGAGGCCCTGGGG A C SPEG Ensembl:ENSG00000072195 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219483269..219483370 32194978 MeRIP-seq:(Medium) rs1453598899 Functional Loss SNV dbSNP153 33..33 33 - - - 84980 RMVar_ID_84980 Human_SNP_ID_113658033 m1A Human chr2 - 219484093 219484093 219484093 TCTGGCCTGGGCTCTGGAGCCTTGTCTTGGGCAGGCTGGGGTGCGGGGGGCTGCGGAGCATCACT TCTGGCCTGGGCTCTGGAGCCTTGTCTTGGGCGGGCTGGGGTGCGGGGGGCTGCGGAGCATCACT T C ASIC4-AS1 Ensembl:ENSG00000227432 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219484045..219484185 26863196 MeRIP-seq:(Medium) rs1408728338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258074 84981 RMVar_ID_84981 Human_SNP_ID_113660284 m1A Human chr2 - 219490634 219490634 219490634 CCTAGAATTCCCAGCTACCTGTCACTGAGCCCACAGAGGAGTTCCCGGTTGCCACAGCTCTCAGC CCTAGAATTCCCAGCTACCTGTCACTGAGCCCCCAGAGGAGTTCCCGGTTGCCACAGCTCTCAGC T G ASIC4-AS1 Ensembl:ENSG00000227432 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219490585..219492630 32194978 MeRIP-seq:(Medium) rs991875217 Functional Loss SNV dbSNP153 33..33 33 - - - 84982 RMVar_ID_84982 Human_SNP_ID_113661082 m1A Human chr2 + 219493270 219493270 219493270 CACAGATACAGTGGCAGGGGCCCAGGGCTGGGACATGAGAGAAGGCAGCGAGGCGGCAGAGGGAG CACAGATACAGTGGCAGGGGCCCAGGGCTGGGTCATGAGAGAAGGCAGCGAGGCGGCAGAGGGAG A T AC053503.6,SPEG Ensembl:ENSG00000286143,Ensembl:ENSG00000072195 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:219493133..219493309 26863196 MeRIP-seq:(Medium) rs377226202 Functional Loss SNV dbSNP153 33..33 33 - - - 84983 RMVar_ID_84983 Human_SNP_ID_113662628 m1A Human chr2 - 219498934 219498934 219498934 CCGCCACCCCTCCACCAGCTCCCTTTACCACTAGCTCCCTTCACTCCAGCTCTGCCGCCCGCTAC CCGCCACCCCTCCACCAGCTCCCTTTACCACTCGCTCCCTTCACTCCAGCTCTGCCGCCCGCTAC T G ASIC4-AS1 Ensembl:ENSG00000227432 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219498884..219499040 26863196 MeRIP-seq:(Medium) rs180718165 Functional Loss SNV dbSNP153 33..33 33 - - - 84984 RMVar_ID_84984 Human_SNP_ID_113663465 m1A Human chr2 + 219502006 219502006 219502006 CTTGAGTGCTATGTTGGAAGCCCACCGACGCCAGCGTCACCCTTTCTTACTCCTTGGCACTACGG CTTGAGTGCTATGTTGGAAGCCCACCGACGCCCGCGTCACCCTTTCTTACTCCTTGGCACTACGG A C GMPPA Ensembl:ENSG00000144591 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219501958..219502069 26863196 MeRIP-seq:(Medium) rs746623283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_363693,Human_Splice_Rec_363703,Human_Splice_Rec_363725,Human_Splice_Rec_363757,Human_Splice_Rec_363781,Human_Splice_Rec_363805,Human_Splice_Rec_363829,Human_Splice_Rec_363839,Human_Splice_Rec_363855,Human_Splice_Rec_363873,Human_Splice_Rec_363885 RMVar_hsa_circ_207113,RMVar_hsa_circ_207111,RMVar_hsa_circ_116886,RMVar_hsa_circ_76900,RMVar_hsa_circ_329357,RMVar_hsa_circ_207112 84985 RMVar_ID_84985 Human_SNP_ID_113664100 m1A Human chr2 - 219504437 219504437 219504437 CTCAGGGCTTAGGAGAAATGGACCAGAAGGGGAGTGGGCAGGCAGTGACAGAGGAGGAACTGGGA CTCAGGGCTTAGGAGAAATGGACCAGAAGGGGTGTGGGCAGGCAGTGACAGAGGAGGAACTGGGA T A ASIC4-AS1 Ensembl:ENSG00000227432 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:219504334..219504461 26863196 MeRIP-seq:(Medium) rs1050035361 Functional Loss SNV dbSNP153 33..33 33 - - - 84986 RMVar_ID_84986 Human_SNP_ID_113664747 m1A Human chr2 + 219506348 219506348 219506348 CGTGGAGGGTACCCCCAGTGACCCTAACCCCAACGATCCCCGAGCCCGCATGGACAGTGAGAGCC CGTGGAGGGTACCCCCAGTGACCCTAACCCCAGCGATCCCCGAGCCCGCATGGACAGTGAGAGCC A G GMPPA Ensembl:ENSG00000144591 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219505960..219506400 32194978 MeRIP-seq:(Medium) rs1559449288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243027,Human_RBP_ID_22450093 Human_Splice_Rec_363714,Human_Splice_Rec_363715,Human_Splice_Rec_363738,Human_Splice_Rec_363739,Human_Splice_Rec_363770,Human_Splice_Rec_363771,Human_Splice_Rec_363794,Human_Splice_Rec_363795,Human_Splice_Rec_363818,Human_Splice_Rec_363819,Human_Splice_Rec_363868,Human_Splice_Rec_363869,Human_Splice_Rec_363878,Human_Splice_Rec_363898,Human_Splice_Rec_363899,Human_Splice_Rec_363904,Human_Splice_Rec_363906 RMVar_hsa_circ_207111,RMVar_hsa_circ_116886,RMVar_hsa_circ_127693,RMVar_hsa_circ_120141,RMVar_hsa_circ_207117,RMVar_hsa_circ_79233,RMVar_hsa_circ_207119,RMVar_hsa_circ_207121 84987 RMVar_ID_84987 Human_SNP_ID_113674216 m1A Human chr2 + 219539786 219539786 219539786 GGGCCACAGCTGGGTGGAAGGCTTGGAAATGCATGGGAAAGAAGGCCTGCCAGCCGGAGATGGCA GGGCCACAGCTGGGTGGAAGGCTTGGAAATGCGTGGGAAAGAAGGCCTGCCAGCCGGAGATGGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219539735..219539884 32194978 MeRIP-seq:(Medium) rs964671223 Functional Loss SNV dbSNP153 33..33 33 - - - 84988 RMVar_ID_84988 Human_SNP_ID_113676709 m1A Human chr2 + 219547312 219547312 219547312 TATGTTTGCCTTCCCATTGACCACCAACAGCCATATCTCTCTAACCTCCCCTGACCTCAATGGCC TATGTTTGCCTTCCCATTGACCACCAACAGCCCTATCTCTCTAACCTCCCCTGACCTCAATGGCC A C TMEM198 Ensembl:ENSG00000188760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219547261..219547478 26863196 MeRIP-seq:(Medium) rs930679232 Functional Loss SNV dbSNP153 33..33 33 - - - 84989 RMVar_ID_84989 Human_SNP_ID_113676710 m1A Human chr2 + 219547312 219547312 219547312 TATGTTTGCCTTCCCATTGACCACCAACAGCCATATCTCTCTAACCTCCCCTGACCTCAATGGCC TATGTTTGCCTTCCCATTGACCACCAACAGCCGTATCTCTCTAACCTCCCCTGACCTCAATGGCC A G TMEM198 Ensembl:ENSG00000188760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219547261..219547478 26863196 MeRIP-seq:(Medium) rs930679232 Functional Loss SNV dbSNP153 33..33 33 - - - 84990 RMVar_ID_84990 Human_SNP_ID_113676711 m1A Human chr2 + 219547312 219547312 219547312 TATGTTTGCCTTCCCATTGACCACCAACAGCCATATCTCTCTAACCTCCCCTGACCTCAATGGCC TATGTTTGCCTTCCCATTGACCACCAACAGCCTTATCTCTCTAACCTCCCCTGACCTCAATGGCC A T TMEM198 Ensembl:ENSG00000188760 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219547261..219547478 26863196 MeRIP-seq:(Medium) rs930679232 Functional Loss SNV dbSNP153 33..33 33 - - - 84991 RMVar_ID_84991 Human_SNP_ID_113678100 m1A Human chr2 - 219551556 219551556 219551556 AAGGCACTTACTGCTGCCAGGCCGGCCAGGACAGCACCCACACACGGCTGCTGGTAGAGGGTGAG AAGGCACTTACTGCTGCCAGGCCGGCCAGGACGGCACCCACACACGGCTGCTGGTAGAGGGTGAG T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219551525..219552287 32194978 MeRIP-seq:(Medium) rs1474277264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_364041,Human_Splice_Rec_364045,Human_Splice_Rec_364051,Human_Splice_Rec_364119 RMVar_hsa_circ_118749,RMVar_hsa_circ_207128,RMVar_hsa_circ_97076,RMVar_hsa_circ_207127 84992 RMVar_ID_84992 Human_SNP_ID_113678355 m1A Human chr2 - 219552114 219552099 219552114 GCCCGCCCAGTCCCTGGCTCTACTGGAAGTGGAGGGTAAGCACCTGGGGTGGGAGCGACAGAGAG GCCCGCCCAGTCCCTGGCTCTACTGGAAGTGG_______________GGTGGGAGCGACAGAGAG CCCAGGTGCTTACCCT C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219552104..219552354 26863196 MeRIP-seq:(Medium) rs748781346 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_4622929 Human_Splice_Rec_364039,Human_Splice_Rec_364043,Human_Splice_Rec_364049,Human_Splice_Rec_364081,Human_Splice_Rec_364117 RMVar_hsa_circ_118749,RMVar_hsa_circ_207128,RMVar_hsa_circ_97076,RMVar_hsa_circ_207127 84993 RMVar_ID_84993 Human_SNP_ID_113678460 m1A Human chr2 - 219552318 219552318 219552318 GCATCCCTGTTCCGCCCACCCTAGCATACACTAACGGCGTCCGAACCGACCCAGGGGCCTGCTGG GCATCCCTGTTCCGCCCACCCTAGCATACACTTACGGCGTCCGAACCGACCCAGGGGCCTGCTGG T A OBSL1 Ensembl:ENSG00000124006 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219551574..219552632 26863196 MeRIP-seq:(Medium) rs937332803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118749,RMVar_hsa_circ_207128,RMVar_hsa_circ_97076,RMVar_hsa_circ_207127 84994 RMVar_ID_84994 Human_SNP_ID_113680319 m1A Human chr2 - 219557442 219557442 219557442 AGGGGCGGGTGCAGCTGGAGCAGGCCGGGGCCAGGCAGGTGCTGCGGGTGCAGGGGGCACGGAGC AGGGGCGGGTGCAGCTGGAGCAGGCCGGGGCCGGGCAGGTGCTGCGGGTGCAGGGGGCACGGAGC T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219557401..219557520 26863196 MeRIP-seq:(Medium) rs1197708190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067761,Human_RBP_ID_5382109,Human_RBP_ID_21980895,Human_RBP_ID_22417280 Human_Splice_Rec_364025,Human_Splice_Rec_364073,Human_Splice_Rec_364143 84995 RMVar_ID_84995 Human_SNP_ID_113680520 m1A Human chr2 - 219557883 219557883 219557883 AGGCTGCAGGCCCAGCCCATGCAGGGCTCTACACCTGCCAGTCTGGAGCAGCCCCCGGAGCCCCA AGGCTGCAGGCCCAGCCCATGCAGGGCTCTACCCCTGCCAGTCTGGAGCAGCCCCCGGAGCCCCA T G OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219557832..219558205 32194978 MeRIP-seq:(Medium) rs745987417 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_364023,Human_Splice_Rec_364071,Human_Splice_Rec_364103,Human_Splice_Rec_364141,Human_Splice_Rec_364151,Human_Splice_Rec_364159 RMVar_hsa_circ_69046 84996 RMVar_ID_84996 Human_SNP_ID_113681072 m1A Human chr2 - 219559325 219559325 219559325 AGCGAGGCCCTGGTGCTGGAGAGGGATGGGCCACGCTGCCGCCTGGTGCTACCTGCTGCTCAGCC AGCGAGGCCCTGGTGCTGGAGAGGGATGGGCCGCGCTGCCGCCTGGTGCTACCTGCTGCTCAGCC T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219559276..219559437 26863196 MeRIP-seq:(Medium) rs1343544868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544794 Human_miRNA_ID_740031,Human_miRNA_ID_744048,Human_miRNA_ID_748054,Human_miRNA_ID_2299416,Human_miRNA_ID_2302688,Human_miRNA_ID_2305951 RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_207130 84997 RMVar_ID_84997 Human_SNP_ID_113681082 m1A Human chr2 + 219559344 219559344 219559344 CCAGGCGGCAGCGTGGCCCATCCCTCTCCAGCACCAGGGCCTCGCTCTCCTCCACTTCCAGCCCA CCAGGCGGCAGCGTGGCCCATCCCTCTCCAGCTCCAGGGCCTCGCTCTCCTCCACTTCCAGCCCA A T AC009955.4 Ensembl:ENSG00000269068 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219559294..219559420 26863196 MeRIP-seq:(Medium) rs770244571 Functional Loss SNV dbSNP153 33..33 33 - - - 84998 RMVar_ID_84998 Human_SNP_ID_113681749 m1A Human chr2 + 219561831 219561831 219561831 GGCTGAAGCAGTCTGGGGAGAGGCAAAAAGCAATGGCAGGGAGGTGGGACAGAGGAATGTGGGCC GGCTGAAGCAGTCTGGGGAGAGGCAAAAAGCAGTGGCAGGGAGGTGGGACAGAGGAATGTGGGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:219561781..219561975 26863196 MeRIP-seq:(Medium) rs548372807 Functional Loss SNV dbSNP153 33..33 33 - - - 84999 RMVar_ID_84999 Human_SNP_ID_113681803 m1A Human chr2 - 219561948 219561948 219561948 TAACAATCCGGAGTTATGCGTCCTCTTGAAAAAGCCGAAGACCCGGCGGCTCTGGTCCCGCTTCC TAACAATCCGGAGTTATGCGTCCTCTTGAAAACGCCGAAGACCCGGCGGCTCTGGTCCCGCTTCC T G OBSL1 Ensembl:ENSG00000124006 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219561791..219562025 26863196 MeRIP-seq:(Medium) rs1362910452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_364180,Human_Splice_Rec_364196 Human_miRNA_ID_3010249 RMVar_hsa_circ_108853,RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_117390,RMVar_hsa_circ_207132,RMVar_hsa_circ_207134,RMVar_hsa_circ_80760,RMVar_hsa_circ_207133,RMVar_hsa_circ_207131 85000 RMVar_ID_85000 Human_SNP_ID_113681815 m1A Human chr2 - 219561975 219561975 219561975 GTCTTACCAAAGTCAGGACAGTTCAAATAACAATCCGGAGTTATGCGTCCTCTTGAAAAAGCCGA GTCTTACCAAAGTCAGGACAGTTCAAATAACAGTCCGGAGTTATGCGTCCTCTTGAAAAAGCCGA T C OBSL1 Ensembl:ENSG00000124006 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:219561926..219561975 26863196 MeRIP-seq:(Medium) rs1415226063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_364180,Human_Splice_Rec_364196 RMVar_hsa_circ_108853,RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_117390,RMVar_hsa_circ_207132,RMVar_hsa_circ_207134,RMVar_hsa_circ_80760,RMVar_hsa_circ_207133,RMVar_hsa_circ_207131 85001 RMVar_ID_85001 Human_SNP_ID_113682359 m1A Human chr2 - 219563453 219563453 219563453 TGACTTCGTGGTGCTGGAGAATGAGGGGCCCCATCGCCGCCTGGTGCTGCCCGCCACCCAGCCCT TGACTTCGTGGTGCTGGAGAATGAGGGGCCCCTTCGCCGCCTGGTGCTGCCCGCCACCCAGCCCT T A OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219563402..219563556 26863196 MeRIP-seq:(Medium) rs1278666318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242677,Human_RBP_ID_919352,Human_RBP_ID_8845898,Human_RBP_ID_9297579,Human_RBP_ID_19000791 Human_Splice_Rec_364015,Human_Splice_Rec_364065,Human_Splice_Rec_364095,Human_Splice_Rec_364133,Human_Splice_Rec_364177,Human_Splice_Rec_364193 RMVar_hsa_circ_61289,RMVar_hsa_circ_108853,RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_207132,RMVar_hsa_circ_207134,RMVar_hsa_circ_80760,RMVar_hsa_circ_207133,RMVar_hsa_circ_373329,RMVar_hsa_circ_207135 85002 RMVar_ID_85002 Human_SNP_ID_113682841 m1A Human chr2 - 219565231 219565231 219565231 TTCTTCGGCGTCACTGTCCAAGGTCAGGAAGCATGCCAGCCTGGGCTCCTCCAGCCAAGGCTGAT TTCTTCGGCGTCACTGTCCAAGGTCAGGAAGCGTGCCAGCCTGGGCTCCTCCAGCCAAGGCTGAT T C OBSL1 Ensembl:ENSG00000124006 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:219565226..219565275 26863196 MeRIP-seq:(Medium) rs62191613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19102895 RMVar_hsa_circ_108853,RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_207132,RMVar_hsa_circ_207134,RMVar_hsa_circ_80760,RMVar_hsa_circ_207133,RMVar_hsa_circ_373329,RMVar_hsa_circ_207135 85003 RMVar_ID_85003 Human_SNP_ID_113682842 m1A Human chr2 - 219565231 219565231 219565231 TTCTTCGGCGTCACTGTCCAAGGTCAGGAAGCATGCCAGCCTGGGCTCCTCCAGCCAAGGCTGAT TTCTTCGGCGTCACTGTCCAAGGTCAGGAAGCCTGCCAGCCTGGGCTCCTCCAGCCAAGGCTGAT T G OBSL1 Ensembl:ENSG00000124006 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:219565226..219565275 26863196 MeRIP-seq:(Medium) rs62191613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19102895 RMVar_hsa_circ_108853,RMVar_hsa_circ_65527,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_207132,RMVar_hsa_circ_207134,RMVar_hsa_circ_80760,RMVar_hsa_circ_207133,RMVar_hsa_circ_373329,RMVar_hsa_circ_207135 85004 RMVar_ID_85004 Human_SNP_ID_113684764 m1A Human chr2 - 219570710 219570710 219570710 ACGGGATGGCCCTGGACGAAGTGTGGGACAGCAGCCACTTCGCGCTCCAGCCGGGCCGCGCCGAG ACGGGATGGCCCTGGACGAAGTGTGGGACAGCGGCCACTTCGCGCTCCAGCCGGGCCGCGCCGAG T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:219570659..219570759 32194978 MeRIP-seq:(Medium) rs758138350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775544,Human_RBP_ID_919366,Human_RBP_ID_3958516,Human_RBP_ID_18470938,Human_RBP_ID_22078375,Human_RBP_ID_22450911 RMVar_hsa_circ_108853,RMVar_hsa_circ_207134,RMVar_hsa_circ_116258,RMVar_hsa_circ_207140 85005 RMVar_ID_85005 Human_SNP_ID_113684780 m1A Human chr2 - 219570748 219570748 219570748 GGGGGGCCTCCCCGAGCCCACACTGTACTGGGAGAAGGACGGGATGGCCCTGGACGAAGTGTGGG GGGGGGCCTCCCCGAGCCCACACTGTACTGGGGGAAGGACGGGATGGCCCTGGACGAAGTGTGGG T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:219570726..219570750 26863196 MeRIP-seq:(Medium) rs1385390265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58472,Human_RBP_ID_775544,Human_RBP_ID_829081,Human_RBP_ID_919367,Human_RBP_ID_3958516,Human_RBP_ID_5196621,Human_RBP_ID_18470938,Human_RBP_ID_21980899,Human_RBP_ID_22078375,Human_RBP_ID_22450912,Human_RBP_ID_22743079 Human_miRNA_ID_342052,Human_miRNA_ID_1967011,Human_miRNA_ID_1967012 RMVar_hsa_circ_108853,RMVar_hsa_circ_207134,RMVar_hsa_circ_116258,RMVar_hsa_circ_207140 85006 RMVar_ID_85006 Human_SNP_ID_113684781 m1A Human chr2 + 219570752 219570752 219570752 CACTTCGTCCAGGGCCATCCCGTCCTTCTCCCAGTACAGTGTGGGCTCGGGGAGGCCCCCCGCCC CACTTCGTCCAGGGCCATCCCGTCCTTCTCCCTGTACAGTGTGGGCTCGGGGAGGCCCCCCGCCC A T INHA Ensembl:ENSG00000123999 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:219570701..219570907 26863196 MeRIP-seq:(Medium) rs772283203 Functional Loss SNV dbSNP153 33..33 33 - - - 85007 RMVar_ID_85007 Human_SNP_ID_113684915 m1A Human chr2 - 219571058 219571058 219571058 GCGGGCAGCAGCTGGCGGCCTCGGAACGCCTGAGCTTCCCGGCGGACGGCGCGGAGCACGGCCTG GCGGGCAGCAGCTGGCGGCCTCGGAACGCCTGCGCTTCCCGGCGGACGGCGCGGAGCACGGCCTG T G OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:219570957..219571108 26863410 MeRIP-seq:(Medium) rs866729003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921277,Human_RBP_ID_4597655,Human_RBP_ID_5196622,Human_RBP_ID_20619144,Human_RBP_ID_22078377,Human_RBP_ID_22450914,Human_RBP_ID_22721589,Human_RBP_ID_22743080 RMVar_hsa_circ_108853,RMVar_hsa_circ_207134,RMVar_hsa_circ_116258,RMVar_hsa_circ_207140 85008 RMVar_ID_85008 Human_SNP_ID_113685081 m1A Human chr2 - 219571358 219571358 219571358 AGGAGGCGAGCCGGGAGCGGGAGGCCCGGGAGAGCTCCGCGGGTCCCCGCGCCCAGTCCCCAGCC AGGAGGCGAGCCGGGAGCGGGAGGCCCGGGAGGGCTCCGCGGGTCCCCGCGCCCAGTCCCCAGCC T C OBSL1 Ensembl:ENSG00000124006 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:219571256..219571461 26863410 MeRIP-seq:(Medium) rs942796420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242690,Human_RBP_ID_828337,Human_RBP_ID_4597672,Human_RBP_ID_5196625,Human_RBP_ID_18422026,Human_RBP_ID_18470939,Human_RBP_ID_22078380,Human_RBP_ID_24560269 RMVar_hsa_circ_108853,RMVar_hsa_circ_207134,RMVar_hsa_circ_116258,RMVar_hsa_circ_207140 85009 RMVar_ID_85009 Human_SNP_ID_113685082 m1A Human chr2 - 219571360 219571360 219571360 TAAGGAGGCGAGCCGGGAGCGGGAGGCCCGGGAGAGCTCCGCGGGTCCCCGCGCCCAGTCCCCAG TAAGGAGGCGAGCCGGGAGCGGGAGGCCCGGGGGAGCTCCGCGGGTCCCCGCGCCCAGTCCCCAG T C OBSL1 Ensembl:ENSG00000124006 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:219571272..219571418 26863410 MeRIP-seq:(Medium) rs1160570826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242690,Human_RBP_ID_828337,Human_RBP_ID_4622934,Human_RBP_ID_5196625,Human_RBP_ID_18422026,Human_RBP_ID_18470939,Human_RBP_ID_22078380,Human_RBP_ID_24560269 RMVar_hsa_circ_108853,RMVar_hsa_circ_207134,RMVar_hsa_circ_116258,RMVar_hsa_circ_207140 85010 RMVar_ID_85010 Human_SNP_ID_113685425 m1A Human chr2 + 219572325 219572325 219572325 GAGTGGAAAGGCCCTGGGCAGACCCTGGCAGAAGGGGCACGGGGCAGGGTGTGAGTTCCCCACTA GAGTGGAAAGGCCCTGGGCAGACCCTGGCAGAGGGGGCACGGGGCAGGGTGTGAGTTCCCCACTA A G INHA Ensembl:ENSG00000123999 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219572188..219572566 26863196 MeRIP-seq:(Medium) rs772889298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622936,Human_RBP_ID_5197962,Human_RBP_ID_5294054,Human_RBP_ID_5471311,Human_RBP_ID_18422494,Human_RBP_ID_18462690,Human_RBP_ID_22450915,Human_RBP_ID_24553176 85011 RMVar_ID_85011 Human_SNP_ID_113686269 m1A Human chr2 - 219574984 219574984 219574984 CAGCAGCACCAGGACGGGGTGGGTCAGCAGAGAGAGAGCAGAGGTGGCCAGGTGCAGCACGGCCC CAGCAGCACCAGGACGGGGTGGGTCAGCAGAGGGAGAGCAGAGGTGGCCAGGTGCAGCACGGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219574887..219575055 26863196 MeRIP-seq:(Medium) rs935096572 Functional Loss SNV dbSNP153 33..33 33 - - - 85012 RMVar_ID_85012 Human_SNP_ID_113686344 m1A Human chr2 - 219575160 219575160 219575160 GGTTCCTCCGGAGGCCTCTGCAGCAGGCGCAGAGCAGAGGGAGACCAAGGCCAGGACATCAGGGG GGTTCCTCCGGAGGCCTCTGCAGCAGGCGCAGGGCAGAGGGAGACCAAGGCCAGGACATCAGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219575115..219575226 32194978 MeRIP-seq:(Medium) rs1250573913 Functional Loss SNV dbSNP153 33..33 33 - - - 85013 RMVar_ID_85013 Human_SNP_ID_113692140 m1A Human chr2 + 219597911 219597911 219597911 GCGCCGGGCAGCTGAGCTGGTAGGAGGACCAGACGGGGAGGTTCGGTATGTCTGACCAGGACTTA GCGCCGGGCAGCTGAGCTGGTAGGAGGACCAGCCGGGGAGGTTCGGTATGTCTGACCAGGACTTA A C STK11IP Ensembl:ENSG00000144589 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:219597884..219598013 26863196 MeRIP-seq:(Medium) rs1445975826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422028,Human_RBP_ID_19003203 Human_Splice_Rec_364207,Human_Splice_Rec_364255 RMVar_hsa_circ_85360,RMVar_hsa_circ_207144 85014 RMVar_ID_85014 Human_SNP_ID_113692147 m1A Human chr2 - 219597925 219597925 219597925 CCTTTCGAGGAACATAAGTCCTGGTCAGACATACCGAACCTCCCCGTCTGGTCCTCCTACCAGCT CCTTTCGAGGAACATAAGTCCTGGTCAGACATGCCGAACCTCCCCGTCTGGTCCTCCTACCAGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:219597883..219597983;chr2:219597892..219598180;chr2:219597903..219598243 26863196 MeRIP-seq:(Medium) rs762236974 Functional Loss SNV dbSNP153 33..33 33 - - - 85015 RMVar_ID_85015 Human_SNP_ID_113694947 m1A Human chr2 - 219607128 219607127 219607128 TTAGTGGGATGAAGCTGACTTACCAGCCGGAGAGGGGTTCAGAGTTCGGGGCTCCGGGTCCGTAT TTAGTGGGATGAAGCTGACTTACCAGCCGGAG_GGGGTTCAGAGTTCGGGGCTCCGGGTCCGTAT CT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:219607095..219607227 26863196 MeRIP-seq:(Medium) rs1353390994 Functional Loss DEL dbSNP153 33..33 33 - - - 85016 RMVar_ID_85016 Human_SNP_ID_113695377 m1A Human chr2 + 219608398 219608397 219608398 GGAACAGGGAGAAGAGGAGGCAGGAGAGGAGGAAGAAGAGGAGCAGGACCAGAAGGAAGTGGAAG GGAACAGGGAGAAGAGGAGGCAGGAGAGGAGG_AGAAGAGGAGCAGGACCAGAAGGAAGTGGAAG GA G STK11IP Ensembl:ENSG00000144589 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219608192..219608645 26863196 MeRIP-seq:(Medium) rs746386751 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_830315,Human_RBP_ID_3958518,Human_RBP_ID_5382118,Human_RBP_ID_19000807 Human_Splice_Rec_364233,Human_Splice_Rec_364291,Human_Splice_Rec_364333 RMVar_hsa_circ_85360,RMVar_hsa_circ_113867,RMVar_hsa_circ_207144,RMVar_hsa_circ_77797,RMVar_hsa_circ_207145,RMVar_hsa_circ_125946,RMVar_hsa_circ_207146,RMVar_hsa_circ_97664,RMVar_hsa_circ_207151,RMVar_hsa_circ_331975,RMVar_hsa_circ_207152,RMVar_hsa_circ_207153 85017 RMVar_ID_85017 Human_SNP_ID_113695378 m1A Human chr2 + 219608398 219608398 219608398 GGAACAGGGAGAAGAGGAGGCAGGAGAGGAGGAAGAAGAGGAGCAGGACCAGAAGGAAGTGGAAG GGAACAGGGAGAAGAGGAGGCAGGAGAGGAGGGAGAAGAGGAGCAGGACCAGAAGGAAGTGGAAG A G STK11IP Ensembl:ENSG00000144589 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219608192..219608645 26863196 MeRIP-seq:(Medium) rs1169588875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830315,Human_RBP_ID_3958518,Human_RBP_ID_5382118,Human_RBP_ID_19000807 Human_Splice_Rec_364233,Human_Splice_Rec_364291,Human_Splice_Rec_364333 RMVar_hsa_circ_85360,RMVar_hsa_circ_113867,RMVar_hsa_circ_207144,RMVar_hsa_circ_77797,RMVar_hsa_circ_207145,RMVar_hsa_circ_125946,RMVar_hsa_circ_207146,RMVar_hsa_circ_97664,RMVar_hsa_circ_207151,RMVar_hsa_circ_331975,RMVar_hsa_circ_207152,RMVar_hsa_circ_207153 85018 RMVar_ID_85018 Human_SNP_ID_113695382 m1A Human chr2 + 219608404 219608402 219608405 GGGAGAAGAGGAGGCAGGAGAGGAGGAAGAAGAGGAGCAGGACCAGAAGGAAGTGGAAGGTGAGC GGGAGAAGAGGAGGCAGGAGAGGAGGAAGAA___GAGCAGGACCAGAAGGAAGTGGAAGGTGAGC AGAG A STK11IP Ensembl:ENSG00000144589 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219608190..219608708 26863196 MeRIP-seq:(Medium) rs747730877 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_830315,Human_RBP_ID_3958518,Human_RBP_ID_19000807 Human_Splice_Rec_364233,Human_Splice_Rec_364291,Human_Splice_Rec_364333 RMVar_hsa_circ_85360,RMVar_hsa_circ_113867,RMVar_hsa_circ_207144,RMVar_hsa_circ_77797,RMVar_hsa_circ_207145,RMVar_hsa_circ_125946,RMVar_hsa_circ_207146,RMVar_hsa_circ_97664,RMVar_hsa_circ_207151,RMVar_hsa_circ_331975,RMVar_hsa_circ_207152,RMVar_hsa_circ_207153 85019 RMVar_ID_85019 Human_SNP_ID_113695511 m1A Human chr2 + 219608695 219608695 219608695 ACTTCTGCCCACCTGTTTGAGGTGGAACTCCAAGCAGCTCGCACCTTGGAGCGACTGGAGCTCCA ACTTCTGCCCACCTGTTTGAGGTGGAACTCCAGGCAGCTCGCACCTTGGAGCGACTGGAGCTCCA A G STK11IP Ensembl:ENSG00000144589 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219608644..219609153 32194978 MeRIP-seq:(Medium) rs1413699463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_364235,Human_Splice_Rec_364293,Human_Splice_Rec_364335 RMVar_hsa_circ_85360,RMVar_hsa_circ_113867,RMVar_hsa_circ_207144,RMVar_hsa_circ_77797,RMVar_hsa_circ_207145,RMVar_hsa_circ_125946,RMVar_hsa_circ_207146,RMVar_hsa_circ_97664,RMVar_hsa_circ_207151,RMVar_hsa_circ_331975,RMVar_hsa_circ_207152,RMVar_hsa_circ_207153 85020 RMVar_ID_85020 Human_SNP_ID_113696780 m1A Human chr2 + 219612652 219612650 219612652 GGTAAAGGAAGCCGCAAATGCATGGAGGCCCGAGAGTGTCGCTGGTGGGGAGAACTGCCCAGGAT GGTAAAGGAAGCCGCAAATGCATGGAGGCCC__GAGTGTCGCTGGTGGGGAGAACTGCCCAGGAT CGA C STK11IP Ensembl:ENSG00000144589 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219612615..219612712 26863196 MeRIP-seq:(Medium) rs1553546289 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_85360,RMVar_hsa_circ_113867,RMVar_hsa_circ_207144,RMVar_hsa_circ_77797,RMVar_hsa_circ_207145,RMVar_hsa_circ_207146,RMVar_hsa_circ_90246,RMVar_hsa_circ_118509,RMVar_hsa_circ_207154,RMVar_hsa_circ_207155 85021 RMVar_ID_85021 Human_SNP_ID_113700691 m1A Human chr2 + 219627574 219627574 219627574 GCGGCGGCGGCGGCGGCGGAGGTGCGGAGCGGAGCGCGAGGAGGTGGAGCCGCGGGCTGCGGGCT GCGGCGGCGGCGGCGGCGGAGGTGCGGAGCGGGGCGCGAGGAGGTGGAGCCGCGGGCTGCGGGCT A G SLC4A3 Ensembl:ENSG00000114923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219627528..219627685 26863196 MeRIP-seq:(Medium) rs1411514789 Functional Loss SNV dbSNP153 33..33 33 - - - 85022 RMVar_ID_85022 Human_SNP_ID_113700728 m1A Human chr2 + 219627686 219627686 219627686 CCGGACGGCAGTCGCGGCTGCGCTCGGGAGAGAGCGCGGGGGACATGGGGCGCGGCGGCCCGCCT CCGGACGGCAGTCGCGGCTGCGCTCGGGAGAGGGCGCGGGGGACATGGGGCGCGGCGGCCCGCCT A G SLC4A3 Ensembl:ENSG00000114923 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219627527..219627716 26863196 MeRIP-seq:(Medium) rs978968381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_364413,Human_Splice_Rec_364457,Human_Splice_Rec_364501,Human_Splice_Rec_364545 85023 RMVar_ID_85023 Human_SNP_ID_114421974 m1A Human chr2 - 222559186 222559185 222559187 AGATCCAAAGCCCGTGCAACAGCGAGAGGAGCAGGGGCCGGGCGGGGGGGGGGGGGGCGCGGTGT AGATCCAAAGCCCGTGCAACAGCGAGAGGAG__GGGGCCGGGCGGGGGGGGGGGGGGCGCGGTGT CTG C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:222559156..222559283 26863196 MeRIP-seq:(Medium) rs1323232865 Functional Loss DEL dbSNP153 32..33 33 - - - 85024 RMVar_ID_85024 Human_SNP_ID_114421975 m1A Human chr2 - 222559186 222559186 222559186 AGATCCAAAGCCCGTGCAACAGCGAGAGGAGCAGGGGCCGGGCGGGGGGGGGGGGGGCGCGGTGT AGATCCAAAGCCCGTGCAACAGCGAGAGGAGCGGGGGCCGGGCGGGGGGGGGGGGGGCGCGGTGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:222559156..222559283 26863196 MeRIP-seq:(Medium) rs1204742257 Functional Loss SNV dbSNP153 33..33 33 - - - 85025 RMVar_ID_85025 Human_SNP_ID_114423192 m1A Human chr2 + 222564103 222564103 222564103 TCTGCCATCTCTGCACGCACAGCGTCATTCCCATCCTTCTTGTTCCTCTCTTGGCAGACATGACC TCTGCCATCTCTGCACGCACAGCGTCATTCCCTTCCTTCTTGTTCCTCTCTTGGCAGACATGACC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:222564060..222564137 26863196 MeRIP-seq:(Medium) rs1255999835 Functional Loss SNV dbSNP153 33..33 33 - - - 85026 RMVar_ID_85026 Human_SNP_ID_114494148 m1A Human chr2 - 222861075 222861075 222861075 CGCCTCCTCGTCCCGGCCCCGGCCGCGTAGACAACTGCAGTGTCGCAGCCCGGCGCAGCCACAGC CGCCTCCTCGTCCCGGCCCCGGCCGCGTAGACGACTGCAGTGTCGCAGCCCGGCGCAGCCACAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:222861037..222861229;chr2:222861026..222861275;chr2:222861026..222861250;chr2:222861026..222861216 26863196 MeRIP-seq:(Medium) rs556711558 Functional Loss SNV dbSNP153 33..33 33 - - - 85027 RMVar_ID_85027 Human_SNP_ID_114494149 m1A Human chr2 - 222861075 222861075 222861075 CGCCTCCTCGTCCCGGCCCCGGCCGCGTAGACAACTGCAGTGTCGCAGCCCGGCGCAGCCACAGC CGCCTCCTCGTCCCGGCCCCGGCCGCGTAGACCACTGCAGTGTCGCAGCCCGGCGCAGCCACAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:222861037..222861229;chr2:222861026..222861275;chr2:222861026..222861250;chr2:222861026..222861216 26863196 MeRIP-seq:(Medium) rs556711558 Functional Loss SNV dbSNP153 33..33 33 - - - 85028 RMVar_ID_85028 Human_SNP_ID_114494213 m1A Human chr2 + 222861291 222861269 222861291 GTGAGTGCGGCGCCGGTTGTGGGAGCGGCGGGAGCCGGTTGGCGGCGCGGCCTCCGCGTGCGGTT GTGAGTGCGGC______________________GCCGGTTGGCGGCGCGGCCTCCGCGTGCGGTT CGCCGGTTGTGGGAGCGGCGGGA C ACSL3 Ensembl:ENSG00000123983 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:222861283..222861765 26863196 MeRIP-seq:(Medium) rs1207888395 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_919378,Human_RBP_ID_5196626,Human_RBP_ID_5380251,Human_RBP_ID_9330825,Human_RBP_ID_17137964,Human_RBP_ID_19098836,Human_RBP_ID_21980902,Human_RBP_ID_22599525 85029 RMVar_ID_85029 Human_SNP_ID_114495028 m1A Human chr2 - 222864377 222864377 222864377 GCCTCCTTCTCTTCTTATTCTATAGCCTCCCCACAGGCAATCTCACCCATACCCATGGTTTGAGC GCCTCCTTCTCTTCTTATTCTATAGCCTCCCCGCAGGCAATCTCACCCATACCCATGGTTTGAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:222864374..222864508 26863196 MeRIP-seq:(Medium) rs1026544710 Functional Loss SNV dbSNP153 33..33 33 - - - 85030 RMVar_ID_85030 Human_SNP_ID_114553229 m1A Human chr2 - 223099638 223099638 223099638 TGATGGATGGCATGATCGCCTTTTCCCATCCCAGCAGCCAGATAAACCATGCCTTATCCCAGGGA TGATGGATGGCATGATCGCCTTTTCCCATCCCGGCAGCCAGATAAACCATGCCTTATCCCAGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:223099592..223099711 26863196 MeRIP-seq:(Medium) rs183950084 Functional Loss SNV dbSNP153 33..33 33 - - - 85031 RMVar_ID_85031 Human_SNP_ID_114734180 m1A Human chr2 - 223837655 223837655 223837655 GCGGGGGGAGCGGGGAGGAGGGCGCGGGGAGGAGGCAGCGGGGAGGAGCGTGCAGGGAGGAGGCA GCGGGGGGAGCGGGGAGGAGGGCGCGGGGAGGCGGCAGCGGGGAGGAGCGTGCAGGGAGGAGGCA T G AP1S3,AC093884.1 Ensembl:ENSG00000152056,Ensembl:ENSG00000286239 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:223837605..223837677 26863196 MeRIP-seq:(Medium) rs376632048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200803 85032 RMVar_ID_85032 Human_SNP_ID_114743204 m1A Human chr2 - 223877328 223877328 223877328 ATAGCAACAGTATCTTTGCTAATCTTACTAATAGATATTGATTAAAAAAAAAAAACCTCAGTACT ATAGCAACAGTATCTTTGCTAATCTTACTAATGGATATTGATTAAAAAAAAAAAACCTCAGTACT T C WDFY1,AC093884.1 Ensembl:ENSG00000085449,Ensembl:ENSG00000286239 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26488235 GWAS_ID_10116,GWAS_ID_10117,GWAS_ID_10118,GWAS_ID_10119,GWAS_ID_10120,GWAS_ID_10121,GWAS_ID_10122,GWAS_ID_10123,GWAS_ID_10124,GWAS_ID_10125,GWAS_ID_10126,GWAS_ID_10127,GWAS_ID_10128,GWAS_ID_10129,GWAS_ID_10130,GWAS_ID_10131,GWAS_ID_10132,GWAS_ID_10133,GWAS_ID_10134,GWAS_ID_10135,GWAS_ID_10136,GWAS_ID_10137,GWAS_ID_10138,GWAS_ID_10139,GWAS_ID_10140,GWAS_ID_10141,GWAS_ID_10142,GWAS_ID_10143,GWAS_ID_10144,GWAS_ID_10145,GWAS_ID_10146,GWAS_ID_10147,GWAS_ID_10148,GWAS_ID_10149,GWAS_ID_10150 RMVar_hsa_circ_100226,RMVar_hsa_circ_207233 85033 RMVar_ID_85033 Human_SNP_ID_114747443 m1A Human chr2 - 223894337 223894337 223894337 ACAAGTGACTGTTGTGTGTGCTGTTTGCAGTGACAAGGTGCAGTCGCTGTGCTACCTTCAGCTCA ACAAGTGACTGTTGTGTGTGCTGTTTGCAGTGGCAAGGTGCAGTCGCTGTGCTACCTTCAGCTCA T C WDFY1,AC093884.1 Ensembl:ENSG00000085449,Ensembl:ENSG00000286239 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:223894301..223894350 32194978 MeRIP-seq:(Medium) rs1432443155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22548688,Human_RBP_ID_22670475 Human_Splice_Rec_365290,Human_Splice_Rec_365324,Human_Splice_Rec_365338,Human_Splice_Rec_365348 Human_miRNA_ID_2750107,Human_miRNA_ID_2750108,Human_miRNA_ID_2750109 RMVar_hsa_circ_29738,RMVar_hsa_circ_100226,RMVar_hsa_circ_119298,RMVar_hsa_circ_207234,RMVar_hsa_circ_378334,RMVar_hsa_circ_207233,RMVar_hsa_circ_377422,RMVar_hsa_circ_207235,RMVar_hsa_circ_302542,RMVar_hsa_circ_207238,RMVar_hsa_circ_207239,RMVar_hsa_circ_296036,RMVar_hsa_circ_374218,RMVar_hsa_circ_207245,RMVar_hsa_circ_107078,RMVar_hsa_circ_207241,RMVar_hsa_circ_207242,RMVar_hsa_circ_271917,RMVar_hsa_circ_348741,RMVar_hsa_circ_285703,RMVar_hsa_circ_121919,RMVar_hsa_circ_207249,RMVar_hsa_circ_84115,RMVar_hsa_circ_207250,RMVar_hsa_circ_207247,RMVar_hsa_circ_207248,RMVar_hsa_circ_207246,RMVar_hsa_circ_207254,RMVar_hsa_circ_279883,RMVar_hsa_circ_335758,RMVar_hsa_circ_207244,RMVar_hsa_circ_353723,RMVar_hsa_circ_307036,RMVar_hsa_circ_109679,RMVar_hsa_circ_276683,RMVar_hsa_circ_207255,RMVar_hsa_circ_207256,RMVar_hsa_circ_207252,RMVar_hsa_circ_207253 85034 RMVar_ID_85034 Human_SNP_ID_114760300 m1A Human chr2 - 223944592 223944592 223944592 CAGCCCGGGAACTCTGTCCCACCGCGCCACTCAAGCCCGGGACCCCGGTTCCAGTGCGCCCCAAC CAGCCCGGGAACTCTGTCCCACCGCGCCACTCTAGCCCGGGACCCCGGTTCCAGTGCGCCCCAAC T A WDFY1,AC093884.1 Ensembl:ENSG00000085449,Ensembl:ENSG00000286239 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:223944588..223944971 26863196 MeRIP-seq:(Medium) rs1392272192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131715,Human_RBP_ID_17084719 RMVar_hsa_circ_109679,RMVar_hsa_circ_207256 85035 RMVar_ID_85035 Human_SNP_ID_114761282 m1A Human chr2 - 223948039 223948039 223948039 GGCTGTCTCTACAAAACCCCTGGCATGTGCTCACCTCAATGCCTTAACACGTGCTCTTTTCTTTT GGCTGTCTCTACAAAACCCCTGGCATGTGCTCCCCTCAATGCCTTAACACGTGCTCTTTTCTTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:223947989..223948122 26863196 MeRIP-seq:(Medium) rs898485131 Functional Loss SNV dbSNP153 33..33 33 - - - 85036 RMVar_ID_85036 Human_SNP_ID_114763456 m1A Human chr2 - 223957531 223957531 223957531 CTCCCCGAACCGGAGGGACCAGCTTGGGGGCGACTGGAGCCAGGAGGCAGCGATGTCCCTGCTGC CTCCCCGAACCGGAGGGACCAGCTTGGGGGCGTCTGGAGCCAGGAGGCAGCGATGTCCCTGCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:223957481..223957650;chr2:223957484..223957604;chr2:223957481..223957641 26863196 MeRIP-seq:(Medium) rs1213464838 Functional Loss SNV dbSNP153 33..33 33 - - - 85037 RMVar_ID_85037 Human_SNP_ID_114763457 m1A Human chr2 - 223957531 223957531 223957531 CTCCCCGAACCGGAGGGACCAGCTTGGGGGCGACTGGAGCCAGGAGGCAGCGATGTCCCTGCTGC CTCCCCGAACCGGAGGGACCAGCTTGGGGGCGGCTGGAGCCAGGAGGCAGCGATGTCCCTGCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:223957481..223957650;chr2:223957484..223957604;chr2:223957481..223957641 26863196 MeRIP-seq:(Medium) rs1213464838 Functional Loss SNV dbSNP153 33..33 33 - - - 85038 RMVar_ID_85038 Human_SNP_ID_114763467 m1A Human chr2 - 223957546 223957546 223957546 GGAATCCCTTCTTCACTCCCCGAACCGGAGGGACCAGCTTGGGGGCGACTGGAGCCAGGAGGCAG GGAATCCCTTCTTCACTCCCCGAACCGGAGGGGCCAGCTTGGGGGCGACTGGAGCCAGGAGGCAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:223957501..223957699 26863196 MeRIP-seq:(Medium) rs754177649 Functional Loss SNV dbSNP153 33..33 33 - - - 85039 RMVar_ID_85039 Human_SNP_ID_114766533 m1A Human chr2 - 223969549 223969548 223969549 CACTATTTAGCGGGGGGGGGGGGGGGGCGGGGAGGGGGAAGAAAAGGATTACTGGGTTTGCAAAT CACTATTTAGCGGGGGGGGGGGGGGGGCGGGG_GGGGGAAGAAAAGGATTACTGGGTTTGCAAAT CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:223969526..223969575 26863196 MeRIP-seq:(Medium) rs1372347351 Functional Loss DEL dbSNP153 33..33 33 - - - 85040 RMVar_ID_85040 Human_SNP_ID_114766537 m1A Human chr2 - 223969549 223969549 223969549 CACTATTTAGCGGGGGGGGGGGGGGGGCGGGGAGGGGGAAGAAAAGGATTACTGGGTTTGCAAAT CACTATTTAGCGGGGGGGGGGGGGGGGCGGGGGGGGGGAAGAAAAGGATTACTGGGTTTGCAAAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:223969526..223969575 26863196 MeRIP-seq:(Medium) rs868547435 Functional Loss SNV dbSNP153 33..33 33 - - - 85041 RMVar_ID_85041 Human_SNP_ID_114784337 m1A Human chr2 + 224039541 224039541 224039541 CCGGAACGCGCCGGGGAGACGCGCAGACCCCGAGGTGCGGCGCCAGCCCGGGCCCAGCTGCACGT CCGGAACGCGCCGGGGAGACGCGCAGACCCCGCGGTGCGGCGCCAGCCCGGGCCCAGCTGCACGT A C lnc-MRPL44-1,lnc-MRPL44-1:2,lnc-MRPL44-1:3 RNACentral:URS00008BCE61,RNACentral:URS0000D5C5D6,RNACentral:URS0000D5D11B lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:224039386..224039561 26863196 MeRIP-seq:(Medium) rs1303819646 Functional Loss SNV dbSNP153 33..33 33 - - - 85042 RMVar_ID_85042 Human_SNP_ID_114918400 m1A Human chr2 - 224585201 224585195 224585201 CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCGAGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGC CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCG______CGCCGCCGCCGCCGCCGCCCCCGCCGC GGCGGCT G CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,Starvation treatment chr2:224584948..224585425;chr2:224585037..224585289;chr2:224585051..224585291;chr2:224585032..224585350;chr2:224585110..224585349 26863196,26863410 MeRIP-seq:(Medium) rs1428627934 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4625152 85043 RMVar_ID_85043 Human_SNP_ID_114918403 m1A Human chr2 - 224585201 224585201 224585201 CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCGAGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGC CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCGCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGC T G CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,Starvation treatment chr2:224584948..224585425;chr2:224585037..224585289;chr2:224585051..224585291;chr2:224585032..224585350;chr2:224585110..224585349 26863196,26863410 MeRIP-seq:(Medium) rs1344350897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625152 85044 RMVar_ID_85044 Human_SNP_ID_114918456 m1A Human chr2 - 224585288 224585288 224585288 CGCCGCCGCCGCCATCGCGGAGGAGCGCGATAAAGGGAGCCGAGCCGGACGTGAGGGGGACCCCG CGCCGCCGCCGCCATCGCGGAGGAGCGCGATAGAGGGAGCCGAGCCGGACGTGAGGGGGACCCCG T C CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:224585251..224585392 26863196 MeRIP-seq:(Medium) rs1175181995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4598458,Human_RBP_ID_5197977,Human_RBP_ID_17951418,Human_RBP_ID_18422030,Human_RBP_ID_22076864,Human_RBP_ID_27819334 85045 RMVar_ID_85045 Human_SNP_ID_114918457 m1A Human chr2 - 224585288 224585288 224585288 CGCCGCCGCCGCCATCGCGGAGGAGCGCGATAAAGGGAGCCGAGCCGGACGTGAGGGGGACCCCG CGCCGCCGCCGCCATCGCGGAGGAGCGCGATACAGGGAGCCGAGCCGGACGTGAGGGGGACCCCG T G CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:224585251..224585392 26863196 MeRIP-seq:(Medium) rs1175181995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4598458,Human_RBP_ID_5197977,Human_RBP_ID_17951418,Human_RBP_ID_18422030,Human_RBP_ID_22076864,Human_RBP_ID_27819334 85046 RMVar_ID_85046 Human_SNP_ID_114918488 m1A Human chr2 + 224585353 224585353 224585353 GCGACGGACAAACATCTCACTGCGCAGGCCGAACGTCGTCCTCCTCCTCCTCCTTCTCCTCCTCC GCGACGGACAAACATCTCACTGCGCAGGCCGAGCGTCGTCCTCCTCCTCCTCCTTCTCCTCCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:224584951..224585400 26863196 MeRIP-seq:(Medium) rs970186610 Functional Loss SNV dbSNP153 33..33 33 - - - 85047 RMVar_ID_85047 Human_SNP_ID_114918493 m1A Human chr2 - 224585356 224585356 224585356 GGCGGAGGAGGAGAAGGAGGAGGAGGAGGACGACGTTCGGCCTGCGCAGTGAGATGTTTGTCCGT GGCGGAGGAGGAGAAGGAGGAGGAGGAGGACGGCGTTCGGCCTGCGCAGTGAGATGTTTGTCCGT T C CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:224584951..224585425;chr2:224584930..224585425 26863196 MeRIP-seq:(Medium) rs1013625134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6891530,Human_RBP_ID_18422030,Human_RBP_ID_18755275 85048 RMVar_ID_85048 Human_SNP_ID_115001740 m1A Human chr2 - 224931666 224931666 224931666 TGATTAATACCATATTTTCTTTTTCTACAGCAAGAAAAGCCTAGGCTTCTCGAGCCTTTGGATTA TGATTAATACCATATTTTCTTTTTCTACAGCAGGAAAAGCCTAGGCTTCTCGAGCCTTTGGATTA T C DOCK10 Ensembl:ENSG00000135905 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:224931641..224931728 26863196 MeRIP-seq:(Medium) rs939536702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_365658,Human_Splice_Rec_365768,Human_Splice_Rec_365878,Human_Splice_Rec_365990,Human_Splice_Rec_366138,Human_Splice_Rec_366170,Human_Splice_Rec_366178 RMVar_hsa_circ_49937,RMVar_hsa_circ_69828,RMVar_hsa_circ_313600,RMVar_hsa_circ_353199 85049 RMVar_ID_85049 Human_SNP_ID_599395622 m1A Human chr16 - 30000962 30000962 30000962 CCTGTTGAAGGAGGCAGGGAGAGGCTGGAGGGAGAGGGGGCGCCCCCCAGCGGAGGGCTTCTCTT CCTGTTGAAGGAGGCAGGGAGAGGCTGGAGGGGGAGGGGGCGCCCCCCAGCGGAGGGCTTCTCTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30000926..30001050 26863196 MeRIP-seq:(Medium) rs1164598069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85050 RMVar_ID_85050 Human_SNP_ID_599395629 m1A Human chr16 - 30000975 30000975 30000975 CTGAAGGGGAAACCCTGTTGAAGGAGGCAGGGAGAGGCTGGAGGGAGAGGGGGCGCCCCCCAGCG CTGAAGGGGAAACCCTGTTGAAGGAGGCAGGGGGAGGCTGGAGGGAGAGGGGGCGCCCCCCAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:30000833..30001551;chr16:30000832..30001651 26863196 MeRIP-seq:(Medium) rs1321181563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85051 RMVar_ID_85051 Human_SNP_ID_599395857 m1A Human chr16 + 30001451 30001451 30001451 CTCCTCCCGCTACCCCCCATTCCCTTCTGACTACCTGGCCCTGCAGCTGCCCGAGCCCAGTCCCC CTCCTCCCGCTACCCCCCATTCCCTTCTGACTGCCTGGCCCTGCAGCTGCCCGAGCCCAGTCCCC A G INO80E Ensembl:ENSG00000169592 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30001426..30001475 26863196 MeRIP-seq:(Medium) rs1311078005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235091,Human_RBP_ID_762872,Human_RBP_ID_4398701,Human_RBP_ID_5113908,Human_RBP_ID_8431942,Human_RBP_ID_12716269,Human_RBP_ID_17078194,Human_RBP_ID_17875150,Human_RBP_ID_18939002,Human_RBP_ID_26440687,Human_RBP_ID_27441208 Human_Splice_Rec_1700972,Human_Splice_Rec_1700973,Human_Splice_Rec_1700988,Human_Splice_Rec_1700999,Human_Splice_Rec_1701011,Human_Splice_Rec_1701025,Human_Splice_Rec_1701036,Human_Splice_Rec_1701037,Human_Splice_Rec_1701072,Human_Splice_Rec_1701073 Human_miRNA_ID_491234,Human_miRNA_ID_494492,Human_miRNA_ID_1194335 85052 RMVar_ID_85052 Human_SNP_ID_599396189 m1A Human chr16 + 30002602 30002602 30002602 GTTCCTGGAGGACCTGGTGTGGGCTGTGCGGGAGAGAGGCCAGGATGCCTCCAGGGCTTTAGTCT GTTCCTGGAGGACCTGGTGTGGGCTGTGCGGGTGAGAGGCCAGGATGCCTCCAGGGCTTTAGTCT A T INO80E Ensembl:ENSG00000169592 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30002078..30002894 26863196 MeRIP-seq:(Medium) rs1355598966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235093,Human_RBP_ID_762878,Human_RBP_ID_1281722,Human_RBP_ID_5142442,Human_RBP_ID_6507312,Human_RBP_ID_12716326,Human_RBP_ID_17188782 85053 RMVar_ID_85053 Human_SNP_ID_599396301 m1A Human chr16 + 30003041 30003041 30003041 CAGAGGTGACAGTACTGGCCCTGGTTCTTAGCAGGGGGGTGGCGGGCAGGGTAGGGGGTGGCGCA CAGAGGTGACAGTACTGGCCCTGGTTCTTAGCGGGGGGGTGGCGGGCAGGGTAGGGGGTGGCGCA A G INO80E Ensembl:ENSG00000169592 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30003038..30003510 26863196 MeRIP-seq:(Medium) rs1370785052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277419 85054 RMVar_ID_85054 Human_SNP_ID_599401902 m1A Human chr16 - 30021189 30021189 30021189 CGTGTGAGGTGCTCTGCCGCAACCCTATGCAGAGAGCAGGTGGGCTAGGACTCGGGGTACTTGCC CGTGTGAGGTGCTCTGCCGCAACCCTATGCAGGGAGCAGGTGGGCTAGGACTCGGGGTACTTGCC T C DOC2A Ensembl:ENSG00000149927 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30021181..30021275 26863196 MeRIP-seq:(Medium) rs1039129436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1701249,Human_Splice_Rec_1701267 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85055 RMVar_ID_85055 Human_SNP_ID_599410673 m1A Human chr16 + 30053715 30053712 30053716 CTGGTATTCCTGGCAAGATAAGGAGTTGACTAAGTAATCCACGAGAAAAGGCATTTCCGGCAGAG CTGGTATTCCTGGCAAGATAAGGAGTTGAC____TAATCCACGAGAAAAGGCATTTCCGGCAGAG CTAAG C AC093512.2 Ensembl:ENSG00000285043 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30053712..30053866 26863196 MeRIP-seq:(Medium) rs951129134 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_80629,RMVar_hsa_circ_88608,RMVar_hsa_circ_90538,RMVar_hsa_circ_177808,RMVar_hsa_circ_104800,RMVar_hsa_circ_177809,RMVar_hsa_circ_177810,RMVar_hsa_circ_177811 85056 RMVar_ID_85056 Human_SNP_ID_599413346 m1A Human chr16 - 30064507 30064507 30064507 CCTATTGATGGGGAGGGAGCCCCTGCCCACTCACCGGTGCTTCAGAGGAAATTCTTCCTTGGAAA CCTATTGATGGGGAGGGAGCCCCTGCCCACTCTCCGGTGCTTCAGAGGAAATTCTTCCTTGGAAA T A AC093512.1 Ensembl:ENSG00000274904 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr16:30064409..30064548;chr16:30064176..30064544;chr16:30064399..30064561;chr16:30064447..30064542 26863410,26863196,26863196,32194978 MeRIP-seq:(Medium) rs112378450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85057 RMVar_ID_85057 Human_SNP_ID_599413839 m1A Human chr16 - 30065888 30065876 30065889 AGGAGAGGGGCGGGTGTGCAGGGTGCGGCGGCAGAGGGCGGCGGGCTGGCGAGTGGATTCAAGGA AGGAGAGGGGCGGGTGTGCAGGGTGCGGCGG_____________GCTGGCGAGTGGATTCAAGGA CCCGCCGCCCTCTG C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:30065789..30065915 26863410 MeRIP-seq:(Medium) rs1242569875 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85058 RMVar_ID_85058 Human_SNP_ID_599413862 m1A Human chr16 + 30065926 30065926 30065926 CGCACCCTGCACACCCGCCCCTCTCCTGTGCCAGGTGAGCGCCCCTCTTCACGTGCGGGGACCAG CGCACCCTGCACACCCGCCCCTCTCCTGTGCCTGGTGAGCGCCCCTCTTCACGTGCGGGGACCAG A T ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30065827..30065980 26863196 MeRIP-seq:(Medium) rs1430310495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760320,Human_RBP_ID_894281,Human_RBP_ID_4393740,Human_RBP_ID_5182687,Human_RBP_ID_9256953,Human_RBP_ID_17371398,Human_RBP_ID_19074055,Human_RBP_ID_22532690,Human_RBP_ID_26811222 Human_Splice_Rec_1701482,Human_Splice_Rec_1701483,Human_Splice_Rec_1701544,Human_Splice_Rec_1701545,Human_Splice_Rec_1701553,Human_Splice_Rec_1701571,Human_Splice_Rec_1701587,Human_Splice_Rec_1701589,Human_Splice_Rec_1701603,Human_Splice_Rec_1701619,Human_Splice_Rec_1701625 RMVar_hsa_circ_85201,RMVar_hsa_circ_80629,RMVar_hsa_circ_88608,RMVar_hsa_circ_90538,RMVar_hsa_circ_177808,RMVar_hsa_circ_104800,RMVar_hsa_circ_177809,RMVar_hsa_circ_123478,RMVar_hsa_circ_177810,RMVar_hsa_circ_177811,RMVar_hsa_circ_177813,RMVar_hsa_circ_102202,RMVar_hsa_circ_177812,RMVar_hsa_circ_76811,RMVar_hsa_circ_101568,RMVar_hsa_circ_15760,RMVar_hsa_circ_177814,RMVar_hsa_circ_104381,RMVar_hsa_circ_177815,RMVar_hsa_circ_177816,RMVar_hsa_circ_177817 85059 RMVar_ID_85059 Human_SNP_ID_599414376 m1A Human chr16 - 30067200 30067200 30067200 TGGATACAGGAAACAGAGGGGAAGGACTAGTTAGCTAGGGTTTCCCATCATCTCCCGATGACCAG TGGATACAGGAAACAGAGGGGAAGGACTAGTTCGCTAGGGTTTCCCATCATCTCCCGATGACCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30067197..30067603 26863196 MeRIP-seq:(Medium) rs762779941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2065815,Human_miRNA_ID_2065816,Human_miRNA_ID_2065817 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85060 RMVar_ID_85060 Human_SNP_ID_599414412 m1A Human chr16 + 30067249 30067249 30067249 CTGTTTCCTGTATCCAGGAACTTGCTACTACCAGCACCATGCCCTACCAATATCCAGCACTGACC CTGTTTCCTGTATCCAGGAACTTGCTACTACCGGCACCATGCCCTACCAATATCCAGCACTGACC A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30067226..30067250 26863196 MeRIP-seq:(Medium) rs371602498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44991,Human_RBP_ID_233805,Human_RBP_ID_472426,Human_RBP_ID_761544,Human_RBP_ID_894283,Human_RBP_ID_1365489,Human_RBP_ID_1516430,Human_RBP_ID_1841241,Human_RBP_ID_4362611,Human_RBP_ID_5419180,Human_RBP_ID_5495470,Human_RBP_ID_8431973,Human_RBP_ID_17253884,Human_RBP_ID_17371400,Human_RBP_ID_17486056,Human_RBP_ID_17875171,Human_RBP_ID_18189949,Human_RBP_ID_18207378,Human_RBP_ID_18677393,Human_RBP_ID_22441933,Human_RBP_ID_22532691,Human_RBP_ID_26810230,Human_RBP_ID_26942590,Human_RBP_ID_27240261,Human_RBP_ID_27441221 Human_Splice_Rec_1701356,Human_Splice_Rec_1701382,Human_Splice_Rec_1701410,Human_Splice_Rec_1701434,Human_Splice_Rec_1701458,Human_Splice_Rec_1701474,Human_Splice_Rec_1701484,Human_Splice_Rec_1701500,Human_Splice_Rec_1701516,Human_Splice_Rec_1701528,Human_Splice_Rec_1701546,Human_Splice_Rec_1701556,Human_Splice_Rec_1701572,Human_Splice_Rec_1701588,Human_Splice_Rec_1701590,Human_Splice_Rec_1701604,Human_Splice_Rec_1701620,Human_Splice_Rec_1701626,Human_Splice_Rec_1701634 Human_miRNA_ID_2493665,Human_miRNA_ID_2493666,Human_miRNA_ID_2493667,Human_miRNA_ID_2696032,Human_miRNA_ID_2696033,Human_miRNA_ID_2696034 RMVar_hsa_circ_85201,RMVar_hsa_circ_80629,RMVar_hsa_circ_88608,RMVar_hsa_circ_90538,RMVar_hsa_circ_177808,RMVar_hsa_circ_104800,RMVar_hsa_circ_177809,RMVar_hsa_circ_123478,RMVar_hsa_circ_177810,RMVar_hsa_circ_177811,RMVar_hsa_circ_177813,RMVar_hsa_circ_102202,RMVar_hsa_circ_177812,RMVar_hsa_circ_76811,RMVar_hsa_circ_101568,RMVar_hsa_circ_15760,RMVar_hsa_circ_177814,RMVar_hsa_circ_104381,RMVar_hsa_circ_177815,RMVar_hsa_circ_177816,RMVar_hsa_circ_324530,RMVar_hsa_circ_348983,RMVar_hsa_circ_376102,RMVar_hsa_circ_177817,RMVar_hsa_circ_371557,RMVar_hsa_circ_345997,RMVar_hsa_circ_96135,RMVar_hsa_circ_297649,RMVar_hsa_circ_177819,RMVar_hsa_circ_177820,RMVar_hsa_circ_177818 85061 RMVar_ID_85061 Human_SNP_ID_599414441 m1A Human chr16 - 30067314 30067314 30067314 AGGATGCCCTTGCCAGGTGCCACGATGCGGTGAGCGATGTCAGACAGCTCCTTCTTCTGCTCCGG AGGATGCCCTTGCCAGGTGCCACGATGCGGTGGGCGATGTCAGACAGCTCCTTCTTCTGCTCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30067214..30067707;chr16:30067187..30067709 26863196 MeRIP-seq:(Medium) rs911754348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2292638,Human_miRNA_ID_2292639,Human_miRNA_ID_2292640,Human_miRNA_ID_2357985,Human_miRNA_ID_2357986,Human_miRNA_ID_2357987,Human_miRNA_ID_2722485,Human_miRNA_ID_2722486,Human_miRNA_ID_2722487,Human_miRNA_ID_3060425,Human_miRNA_ID_3060426,Human_miRNA_ID_3060427 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85062 RMVar_ID_85062 Human_SNP_ID_599414467 m1A Human chr16 - 30067368 30067368 30067368 TGCACCCTCCACCCATTCTGTCTCCTGCCCGCACCAGTGGACTCATCTGCAGCCAGGATGCCCTT TGCACCCTCCACCCATTCTGTCTCCTGCCCGCCCCAGTGGACTCATCTGCAGCCAGGATGCCCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30067326..30067375 32194978 MeRIP-seq:(Medium) rs879193147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2969400,Human_miRNA_ID_2969401,Human_miRNA_ID_2969402 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85063 RMVar_ID_85063 Human_SNP_ID_599414593 m1A Human chr16 + 30067625 30067625 30067625 CAGAAGGCGGATGATGGGCGTCCCTTCCCCCAAGTTATCAAATCCAAGGGCGGTGTTGTGGGCAT CAGAAGGCGGATGATGGGCGTCCCTTCCCCCAGGTTATCAAATCCAAGGGCGGTGTTGTGGGCAT A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30067576..30067625 32194978 MeRIP-seq:(Medium) rs765436514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233807,Human_RBP_ID_472437,Human_RBP_ID_761545,Human_RBP_ID_1003968,Human_RBP_ID_4398736,Human_RBP_ID_6507380,Human_RBP_ID_9061719,Human_RBP_ID_9256957,Human_RBP_ID_17253888,Human_RBP_ID_17369470,Human_RBP_ID_17486060,Human_RBP_ID_17690068,Human_RBP_ID_17875178,Human_RBP_ID_18189965,Human_RBP_ID_18677399,Human_RBP_ID_19071331,Human_RBP_ID_22441437,Human_RBP_ID_22497682,Human_RBP_ID_22532694,Human_RBP_ID_23128114,Human_RBP_ID_26810254,Human_RBP_ID_27155891,Human_RBP_ID_27240268 Human_Splice_Rec_1701359,Human_Splice_Rec_1701385,Human_Splice_Rec_1701413,Human_Splice_Rec_1701437,Human_Splice_Rec_1701475,Human_Splice_Rec_1701487,Human_Splice_Rec_1701503,Human_Splice_Rec_1701531,Human_Splice_Rec_1701549,Human_Splice_Rec_1701559,Human_Splice_Rec_1701575,Human_Splice_Rec_1701593,Human_Splice_Rec_1701607,Human_Splice_Rec_1701623,Human_Splice_Rec_1701627,Human_Splice_Rec_1701637,Human_Splice_Rec_1701645 Human_miRNA_ID_1967884,Human_miRNA_ID_1967885,Human_miRNA_ID_1967886 RMVar_hsa_circ_105537,RMVar_hsa_circ_85201,RMVar_hsa_circ_80629,RMVar_hsa_circ_88608,RMVar_hsa_circ_104800,RMVar_hsa_circ_177809,RMVar_hsa_circ_123478,RMVar_hsa_circ_177810,RMVar_hsa_circ_177811,RMVar_hsa_circ_177813,RMVar_hsa_circ_102202,RMVar_hsa_circ_177812,RMVar_hsa_circ_76811,RMVar_hsa_circ_101568,RMVar_hsa_circ_15760,RMVar_hsa_circ_177814,RMVar_hsa_circ_104381,RMVar_hsa_circ_177815,RMVar_hsa_circ_177816,RMVar_hsa_circ_324530,RMVar_hsa_circ_348983,RMVar_hsa_circ_376102,RMVar_hsa_circ_177817,RMVar_hsa_circ_345997,RMVar_hsa_circ_96135,RMVar_hsa_circ_297649,RMVar_hsa_circ_177819,RMVar_hsa_circ_177820,RMVar_hsa_circ_177822,RMVar_hsa_circ_105294,RMVar_hsa_circ_177821 85064 RMVar_ID_85064 Human_SNP_ID_599414976 m1A Human chr16 - 30068716 30068715 30068716 AACCTGCTCTGGTTGGGTTCGTAGGGCAGAGAATCAAACAGTTCTCACCTTGGGTGGTAGTCTCG AACCTGCTCTGGTTGGGTTCGTAGGGCAGAGA_TCAAACAGTTCTCACCTTGGGTGGTAGTCTCG AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:30068713..30068806;chr16:30068714..30068828 26863196 MeRIP-seq:(Medium) rs886051891 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_442 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85065 RMVar_ID_85065 Human_SNP_ID_599415318 m1A Human chr16 + 30069587 30069587 30069587 CTTGCTGAAGCCCAACATGGTCACCCCAGGCCATGCTTGCACTCAGAAGTTTTCTCATGAGGAGA CTTGCTGAAGCCCAACATGGTCACCCCAGGCCGTGCTTGCACTCAGAAGTTTTCTCATGAGGAGA A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30069537..30069850 26863196 MeRIP-seq:(Medium) rs770093075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45003,Human_RBP_ID_472452,Human_RBP_ID_760321,Human_RBP_ID_1516453,Human_RBP_ID_1841253,Human_RBP_ID_3494093,Human_RBP_ID_4362640,Human_RBP_ID_6507393,Human_RBP_ID_8431994,Human_RBP_ID_17253892,Human_RBP_ID_17690071,Human_RBP_ID_18677415,Human_RBP_ID_22440955,Human_RBP_ID_22760245 Human_Splice_Rec_1701366,Human_Splice_Rec_1701367,Human_Splice_Rec_1701392,Human_Splice_Rec_1701393,Human_Splice_Rec_1701420,Human_Splice_Rec_1701421,Human_Splice_Rec_1701444,Human_Splice_Rec_1701445,Human_Splice_Rec_1701494,Human_Splice_Rec_1701495,Human_Splice_Rec_1701510,Human_Splice_Rec_1701511,Human_Splice_Rec_1701522,Human_Splice_Rec_1701523,Human_Splice_Rec_1701538,Human_Splice_Rec_1701539,Human_Splice_Rec_1701566,Human_Splice_Rec_1701567,Human_Splice_Rec_1701582,Human_Splice_Rec_1701583,Human_Splice_Rec_1701600,Human_Splice_Rec_1701601,Human_Splice_Rec_1701614,Human_Splice_Rec_1701615,Human_Splice_Rec_1701644,Human_Splice_Rec_1701650,Human_Splice_Rec_1701651,Human_Splice_Rec_1701656,Human_Splice_Rec_1701657,Human_Splice_Rec_1701661 Human_miRNA_ID_2019913,Human_miRNA_ID_2019914,Human_miRNA_ID_2025008,Human_miRNA_ID_2025009,Human_miRNA_ID_2311625,Human_miRNA_ID_2311626,Human_miRNA_ID_2313642,Human_miRNA_ID_2313643,Human_miRNA_ID_2499738,Human_miRNA_ID_2499739,Human_miRNA_ID_2607521,Human_miRNA_ID_2607522,Human_miRNA_ID_2655429,Human_miRNA_ID_2655430 RMVar_hsa_circ_38019,RMVar_hsa_circ_15760,RMVar_hsa_circ_104381,RMVar_hsa_circ_177816,RMVar_hsa_circ_324530,RMVar_hsa_circ_96135,RMVar_hsa_circ_297649,RMVar_hsa_circ_177820,RMVar_hsa_circ_373226,RMVar_hsa_circ_177823,RMVar_hsa_circ_116494,RMVar_hsa_circ_76386,RMVar_hsa_circ_177824,RMVar_hsa_circ_177825,RMVar_hsa_circ_114630,RMVar_hsa_circ_365512,RMVar_hsa_circ_82249,RMVar_hsa_circ_177828,RMVar_hsa_circ_177829,RMVar_hsa_circ_177830 85066 RMVar_ID_85066 Human_SNP_ID_599415346 m1A Human chr16 + 30069639 30069639 30069639 TCTCATGAGGAGATTGCCATGGCGACCGTCACAGCGCTGCGCCGCACAGTGCCCCCCGCTGTCAC TCTCATGAGGAGATTGCCATGGCGACCGTCACGGCGCTGCGCCGCACAGTGCCCCCCGCTGTCAC A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30069491..30069676 26863196 MeRIP-seq:(Medium) rs1448266956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233814,Human_RBP_ID_472453,Human_RBP_ID_761551,Human_RBP_ID_817125,Human_RBP_ID_894291,Human_RBP_ID_1516454,Human_RBP_ID_1841253,Human_RBP_ID_4362640,Human_RBP_ID_9061723,Human_RBP_ID_9256972,Human_RBP_ID_18189987,Human_RBP_ID_22440956,Human_RBP_ID_22532697,Human_RBP_ID_22800954,Human_RBP_ID_23686353,Human_RBP_ID_26942610,Human_RBP_ID_27240280,Human_RBP_ID_27441246 Human_Splice_Rec_1701367,Human_Splice_Rec_1701393,Human_Splice_Rec_1701421,Human_Splice_Rec_1701445,Human_Splice_Rec_1701495,Human_Splice_Rec_1701511,Human_Splice_Rec_1701523,Human_Splice_Rec_1701539,Human_Splice_Rec_1701567,Human_Splice_Rec_1701583,Human_Splice_Rec_1701601,Human_Splice_Rec_1701615,Human_Splice_Rec_1701651,Human_Splice_Rec_1701657,Human_Splice_Rec_1701661 Human_miRNA_ID_2077194,Human_miRNA_ID_2077195 RMVar_hsa_circ_38019,RMVar_hsa_circ_15760,RMVar_hsa_circ_104381,RMVar_hsa_circ_177816,RMVar_hsa_circ_324530,RMVar_hsa_circ_96135,RMVar_hsa_circ_297649,RMVar_hsa_circ_177820,RMVar_hsa_circ_373226,RMVar_hsa_circ_177823,RMVar_hsa_circ_116494,RMVar_hsa_circ_76386,RMVar_hsa_circ_177824,RMVar_hsa_circ_177825,RMVar_hsa_circ_114630,RMVar_hsa_circ_365512,RMVar_hsa_circ_82249,RMVar_hsa_circ_177828,RMVar_hsa_circ_177829,RMVar_hsa_circ_177830 85067 RMVar_ID_85067 Human_SNP_ID_599415368 m1A Human chr16 - 30069675 30069675 30069675 ACTGCATAGAGATCAAGATGAGTGTGGGCCTCACCAGTGACAGCGGGGGGCACTGTGCGGCGCAG ACTGCATAGAGATCAAGATGAGTGTGGGCCTCTCCAGTGACAGCGGGGGGCACTGTGCGGCGCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30069501..30069900 26863410 MeRIP-seq:(Medium) rs113222518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85068 RMVar_ID_85068 Human_SNP_ID_599415369 m1A Human chr16 - 30069675 30069675 30069675 ACTGCATAGAGATCAAGATGAGTGTGGGCCTCACCAGTGACAGCGGGGGGCACTGTGCGGCGCAG ACTGCATAGAGATCAAGATGAGTGTGGGCCTCCCCAGTGACAGCGGGGGGCACTGTGCGGCGCAG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30069501..30069900 26863410 MeRIP-seq:(Medium) rs113222518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85069 RMVar_ID_85069 Human_SNP_ID_599415546 m1A Human chr16 - 30070031 30070031 30070031 CCAGGCACCCTGCCCACCTCCTGCCTATCCTTACCAGGGCTCGCTTGACATACTCCTCCTGCGCA CCAGGCACCCTGCCCACCTCCTGCCTATCCTTGCCAGGGCTCGCTTGACATACTCCTCCTGCGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30069980..30070334 26863196 MeRIP-seq:(Medium) rs878921000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85070 RMVar_ID_85070 Human_SNP_ID_599415643 m1A Human chr16 + 30070212 30070212 30070212 GAGTCCCTCTTCGTCTCTAACCACGCCTATTAAGCGGAGGTGTTCCCAGGCTGCCCCCAACACTC GAGTCCCTCTTCGTCTCTAACCACGCCTATTAGGCGGAGGTGTTCCCAGGCTGCCCCCAACACTC A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding stop codon,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30070101..30070400 32194978 MeRIP-seq:(Medium) rs1158197949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45005,Human_RBP_ID_472461,Human_RBP_ID_1516459,Human_RBP_ID_1841260,Human_RBP_ID_3494094,Human_RBP_ID_4398763,Human_RBP_ID_6507402,Human_RBP_ID_8432006,Human_RBP_ID_8806819,Human_RBP_ID_9061724,Human_RBP_ID_17253896,Human_RBP_ID_17486063,Human_RBP_ID_17652986,Human_RBP_ID_18190004,Human_RBP_ID_18677421,Human_RBP_ID_22441459,Human_RBP_ID_22532700,Human_RBP_ID_22800958,Human_RBP_ID_22938330,Human_RBP_ID_23686357,Human_RBP_ID_24413107,Human_RBP_ID_24476094,Human_RBP_ID_26440718,Human_RBP_ID_26811273,Human_RBP_ID_26942616,Human_RBP_ID_27240287,Human_RBP_ID_27441252 Human_Splice_Rec_1701370,Human_Splice_Rec_1701396,Human_Splice_Rec_1701424,Human_Splice_Rec_1701448,Human_Splice_Rec_1701498,Human_Splice_Rec_1701514,Human_Splice_Rec_1701526,Human_Splice_Rec_1701542,Human_Splice_Rec_1701570,Human_Splice_Rec_1701586,Human_Splice_Rec_1701618,Human_Splice_Rec_1701660,Human_Splice_Rec_1701664,Human_Splice_Rec_1701665 Human_miRNA_ID_2016706,Human_miRNA_ID_2016707 RMVar_hsa_circ_104381,RMVar_hsa_circ_177816,RMVar_hsa_circ_96135,RMVar_hsa_circ_177820,RMVar_hsa_circ_116494,RMVar_hsa_circ_177824,RMVar_hsa_circ_114630,RMVar_hsa_circ_82249,RMVar_hsa_circ_177829,RMVar_hsa_circ_67646,RMVar_hsa_circ_177830,RMVar_hsa_circ_92516,RMVar_hsa_circ_177831 85071 RMVar_ID_85071 Human_SNP_ID_599415732 m1A Human chr16 + 30070383 30070383 30070383 CTGTGAATGCTAAGTCCATCACCCTTTCCGGCACACTGCCAAATAAACAGCTATTTAAGGGGGAG CTGTGAATGCTAAGTCCATCACCCTTTCCGGCCCACTGCCAAATAAACAGCTATTTAAGGGGGAG A C ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30070376..30070425 26863196 MeRIP-seq:(Medium) rs1223292215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45007,Human_RBP_ID_472462,Human_RBP_ID_1003986,Human_RBP_ID_1238034,Human_RBP_ID_1841261,Human_RBP_ID_8806821,Human_RBP_ID_9061728,Human_RBP_ID_17253898,Human_RBP_ID_17369473,Human_RBP_ID_17486066,Human_RBP_ID_17875189,Human_RBP_ID_18190505,Human_RBP_ID_18199854,Human_RBP_ID_18207379,Human_RBP_ID_23209324,Human_RBP_ID_23686360,Human_RBP_ID_26636919,Human_RBP_ID_26748956,Human_RBP_ID_26810272,Human_RBP_ID_27441258 Human_miRNA_ID_2457983,Human_miRNA_ID_2457984,Human_miRNA_ID_2462908,Human_miRNA_ID_2462909,Human_miRNA_ID_2635548,Human_miRNA_ID_2635549,Human_miRNA_ID_2638235,Human_miRNA_ID_2638236 RMVar_hsa_circ_104381,RMVar_hsa_circ_177816,RMVar_hsa_circ_96135,RMVar_hsa_circ_177820,RMVar_hsa_circ_116494,RMVar_hsa_circ_177824,RMVar_hsa_circ_114630,RMVar_hsa_circ_82249,RMVar_hsa_circ_177829,RMVar_hsa_circ_177830,RMVar_hsa_circ_92516,RMVar_hsa_circ_177831 85072 RMVar_ID_85072 Human_SNP_ID_599417534 m1A Human chr16 + 30076058 30076058 30076058 CGGCGGTCGAAAGCGGAGTGAAAGAGGGAGGCAGGGAGCCGGAGAGCCGGAACCGGAGTCGCAGC CGGCGGTCGAAAGCGGAGTGAAAGAGGGAGGCGGGGAGCCGGAGAGCCGGAACCGGAGTCGCAGC A G PPP4C Ensembl:ENSG00000149923 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:30075976..30076167;chr16:30075976..30076200;chr16:30075976..30076185;chr16:30075975..30076548 26863196 MeRIP-seq:(Medium) rs1000492029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817807,Human_RBP_ID_893664,Human_RBP_ID_1516461,Human_RBP_ID_3947565,Human_RBP_ID_4362662,Human_RBP_ID_5316637,Human_RBP_ID_6507423,Human_RBP_ID_22442498,Human_RBP_ID_22532813,Human_RBP_ID_23686364,Human_RBP_ID_26328881 Human_Splice_Rec_1701667,Human_Splice_Rec_1701679,Human_Splice_Rec_1701695,Human_Splice_Rec_1701705,Human_Splice_Rec_1701713,Human_Splice_Rec_1701725,Human_Splice_Rec_1701731,Human_Splice_Rec_1701745,Human_Splice_Rec_1701761,Human_Splice_Rec_1701775,Human_Splice_Rec_1701793,Human_Splice_Rec_1701797 RMVar_hsa_circ_102602,RMVar_hsa_circ_177832,RMVar_hsa_circ_89826,RMVar_hsa_circ_177833 85073 RMVar_ID_85073 Human_SNP_ID_599417549 m1A Human chr16 - 30076096 30076096 30076096 AGGACGGTGACTTAGAGGAGTCTCGCACTATTACCGCCGCTGCGACTCCGGTTCCGGCTCTCCGG AGGACGGTGACTTAGAGGAGTCTCGCACTATTTCCGCCGCTGCGACTCCGGTTCCGGCTCTCCGG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEK293T,untreat control chr16:30076001..30076155;chr16:30076001..30076156;chr16:30076025..30076129;chr16:30076001..30076144 26863410 MeRIP-seq:(Medium) rs112397270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85074 RMVar_ID_85074 Human_SNP_ID_599417634 m1A Human chr16 + 30076280 30076280 30076280 GAATCGAGTTGTCCGCTCCGAGCCCCGGACGGACACTGATCCGCGGGCTCGTCTTGGCCTTTCCC GAATCGAGTTGTCCGCTCCGAGCCCCGGACGGCCACTGATCCGCGGGCTCGTCTTGGCCTTTCCC A C PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:30076276..30076405 26863410 MeRIP-seq:(Medium) rs1161299945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5360113,Human_RBP_ID_5440391,Human_RBP_ID_22473822 RMVar_hsa_circ_102602,RMVar_hsa_circ_177832,RMVar_hsa_circ_89826,RMVar_hsa_circ_177833 85075 RMVar_ID_85075 Human_SNP_ID_599417687 m1A Human chr16 + 30076400 30076400 30076400 GGGGTGGGCCATGGCGGAGATCAGCGACCTGGACCGGCAGATCGAGCAGCTGCGTCGCTGCGAGC GGGGTGGGCCATGGCGGAGATCAGCGACCTGGTCCGGCAGATCGAGCAGCTGCGTCGCTGCGAGC A T PPP4C Ensembl:ENSG00000149923 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30076376..30076400 26863196 MeRIP-seq:(Medium) rs1426663705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472473,Human_RBP_ID_817808,Human_RBP_ID_1516462,Human_RBP_ID_4362668,Human_RBP_ID_5317514,Human_RBP_ID_5357948,Human_RBP_ID_6507427,Human_RBP_ID_8432020,Human_RBP_ID_8806823,Human_RBP_ID_9061729,Human_RBP_ID_12716633,Human_RBP_ID_17652991,Human_RBP_ID_17875197,Human_RBP_ID_18986019,Human_RBP_ID_22441461,Human_RBP_ID_22497687,Human_RBP_ID_26328130 Human_Splice_Rec_1701668,Human_Splice_Rec_1701669,Human_Splice_Rec_1701680,Human_Splice_Rec_1701681,Human_Splice_Rec_1701696,Human_Splice_Rec_1701697,Human_Splice_Rec_1701706,Human_Splice_Rec_1701707,Human_Splice_Rec_1701714,Human_Splice_Rec_1701715,Human_Splice_Rec_1701726,Human_Splice_Rec_1701727,Human_Splice_Rec_1701732,Human_Splice_Rec_1701733,Human_Splice_Rec_1701746,Human_Splice_Rec_1701747,Human_Splice_Rec_1701762,Human_Splice_Rec_1701763,Human_Splice_Rec_1701776,Human_Splice_Rec_1701777,Human_Splice_Rec_1701789,Human_Splice_Rec_1701794,Human_Splice_Rec_1701795,Human_Splice_Rec_1701798,Human_Splice_Rec_1701799,Human_Splice_Rec_1701809 RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177832,RMVar_hsa_circ_89826,RMVar_hsa_circ_177833,RMVar_hsa_circ_125702,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177837,RMVar_hsa_circ_177835 85076 RMVar_ID_85076 Human_SNP_ID_599417886 m1A Human chr16 + 30077049 30077049 30077049 TGCAAAAAGGTGGAGTTGGATCATTCACGTTCAGGGTGGGAGCCTGAGAAATCGTAGCAAGTAAG TGCAAAAAGGTGGAGTTGGATCATTCACGTTCGGGGTGGGAGCCTGAGAAATCGTAGCAAGTAAG A G PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30077046..30077121 26863196 MeRIP-seq:(Medium) rs558408717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12716646 RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177833,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177835 85077 RMVar_ID_85077 Human_SNP_ID_599418945 m1A Human chr16 + 30080991 30080991 30080991 GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGAGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGCGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA A C PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30080982..30081300 26863196 MeRIP-seq:(Medium) rs200223896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177833,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177835 85078 RMVar_ID_85078 Human_SNP_ID_599418946 m1A Human chr16 + 30080991 30080991 30080991 GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGAGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGGGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA A G PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30080982..30081300 26863196 MeRIP-seq:(Medium) rs200223896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177833,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177835 85079 RMVar_ID_85079 Human_SNP_ID_599418947 m1A Human chr16 + 30080991 30080991 30080991 GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGAGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGTGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA A T PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30080982..30081300 26863196 MeRIP-seq:(Medium) rs200223896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177833,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177835 85080 RMVar_ID_85080 Human_SNP_ID_599419448 m1A Human chr16 - 30082487 30082487 30082487 GAGGTCATAGAATTGTCCATGGATGTCGCCGCACACCTGGGGAACAGGAAGAGTGGGGTTGGAAC GAGGTCATAGAATTGTCCATGGATGTCGCCGCCCACCTGGGGAACAGGAAGAGTGGGGTTGGAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30082476..30082550 26863196 MeRIP-seq:(Medium) rs866464372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85081 RMVar_ID_85081 Human_SNP_ID_599419665 m1A Human chr16 - 30083154 30083151 30083155 ATGAACCTAATGGCTCTTCTTTCACCTACCAGACACAGACCGGGTCCCTAGCAAGGCACCCAGGC ATGAACCTAATGGCTCTTCTTTCACCTACCA____CAGACCGGGTCCCTAGCAAGGCACCCAGGC GTGTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30083148..30083374 26863196 MeRIP-seq:(Medium) rs1023904237 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85082 RMVar_ID_85082 Human_SNP_ID_599419684 m1A Human chr16 - 30083244 30083244 30083244 GCACCTCTTGCCTGAATCGTGTGGCATCAGCCACCTCCCAGGCCCACACGACCCCTCCAGAGAAT GCACCTCTTGCCTGAATCGTGTGGCATCAGCCGCCTCCCAGGCCCACACGACCCCTCCAGAGAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30083238..30083372 26863196 MeRIP-seq:(Medium) rs1170936193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85083 RMVar_ID_85083 Human_SNP_ID_599420140 m1A Human chr16 - 30084769 30084769 30084769 CACTTGTAACCTTCCATCACCAGTTGGTGGGCACGGCAGATCATGTCAATGTCATTGGCTGCGTT CACTTGTAACCTTCCATCACCAGTTGGTGGGCGCGGCAGATCATGTCAATGTCATTGGCTGCGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:30084718..30084817;chr16:30084718..30084917 26863196 MeRIP-seq:(Medium) rs1386724083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85084 RMVar_ID_85084 Human_SNP_ID_599420236 m1A Human chr16 - 30085077 30085077 30085077 GTGGTGCGAGGGCCAGAAGGGTTGGAGGGGGCAGGGGCCGGGCGGGGTCACAGGAAGTAGTCGGC GTGGTGCGAGGGCCAGAAGGGTTGGAGGGGGCGGGGGCCGGGCGGGGTCACAGGAAGTAGTCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr16:30084951..30085275;chr16:30084980..30085278 26863196,26863410 MeRIP-seq:(Medium) rs1160943070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85085 RMVar_ID_85085 Human_SNP_ID_599422762 m1A Human chr16 - 30092660 30092660 30092660 CATGTGGCTCCAGCCCGGCCTGGCCGCCAGGGAGCGCCACTGGCTTCCCGCCACCCGAAGGGAGC CATGTGGCTCCAGCCCGGCCTGGCCGCCAGGGGGCGCCACTGGCTTCCCGCCACCCGAAGGGAGC T C YPEL3 Ensembl:ENSG00000090238 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30092611..30092711 32194978 MeRIP-seq:(Medium) rs751615939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472522,Human_RBP_ID_5114210,Human_RBP_ID_5524310,Human_RBP_ID_21889207 Human_miRNA_ID_3004515,Human_miRNA_ID_3004516,Human_miRNA_ID_3004517,Human_miRNA_ID_3004518 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_78580,RMVar_hsa_circ_112040,RMVar_hsa_circ_109141,RMVar_hsa_circ_177842,RMVar_hsa_circ_177843,RMVar_hsa_circ_177844 85086 RMVar_ID_85086 Human_SNP_ID_599423809 m1A Human chr16 - 30096172 30096172 30096172 TCCAGGCGCCTGCGAACCCGGGCCCGGGGGGGACGGCGCCCGCCAGGAGCGCCCCCCACTCCCAG TCCAGGCGCCTGCGAACCCGGGCCCGGGGGGGGCGGCGCCCGCCAGGAGCGCCCCCCACTCCCAG T C YPEL3 Ensembl:ENSG00000090238 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30096050..30096193 26863196 MeRIP-seq:(Medium) rs1019074249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393000,Human_RBP_ID_5114212,Human_RBP_ID_5142214 Human_Splice_Rec_1701887,Human_Splice_Rec_1701901,Human_Splice_Rec_1701907,Human_Splice_Rec_1701939,Human_Splice_Rec_1701953 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_109141,RMVar_hsa_circ_177844 85087 RMVar_ID_85087 Human_SNP_ID_599428418 m1A Human chr16 + 30113196 30113196 30113196 GCCTCACCTCCCCAGCCAGCCCAGGCTGCGCCAGCATCTTCTTCCTCGTCCACACCCTGCCCTGC GCCTCACCTCCCCAGCCAGCCCAGGCTGCGCCGGCATCTTCTTCCTCGTCCACACCCTGCCCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30113194..30113302 26863196 MeRIP-seq:(Medium) rs1467743422 Functional Loss SNV dbSNP153 33..33 33 - - - 85088 RMVar_ID_85088 Human_SNP_ID_599428744 m1A Human chr16 - 30114268 30114268 30114268 TTAGTCTCAAGGGCTAGCATCCCTGAGGAGCCAGGCCGGGCCGAATCCCCTCCCTGTCAAAGCTG TTAGTCTCAAGGGCTAGCATCCCTGAGGAGCCGGGCCGGGCCGAATCCCCTCCCTGTCAAAGCTG T C MAPK3 Ensembl:ENSG00000102882 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30114154..30114502 26863196 MeRIP-seq:(Medium) rs1402183035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472534,Human_RBP_ID_894030,Human_RBP_ID_5113465,Human_RBP_ID_17256021,Human_RBP_ID_17371409,Human_RBP_ID_17652999,Human_RBP_ID_18940194,Human_RBP_ID_23209615 Human_miRNA_ID_335689,Human_miRNA_ID_2083986,Human_miRNA_ID_2083987,Human_miRNA_ID_2083988,Human_miRNA_ID_2690584,Human_miRNA_ID_2690585,Human_miRNA_ID_2690586 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85089 RMVar_ID_85089 Human_SNP_ID_599429336 m1A Human chr16 - 30116612 30116612 30116612 TGGGGCCTGGTGAGTGTCTCCATGGCCCACACATGGACACCCTGATACTAAATATCTATATCTGT TGGGGCCTGGTGAGTGTCTCCATGGCCCACACGTGGACACCCTGATACTAAATATCTATATCTGT T C MAPK3 Ensembl:ENSG00000102882 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30116610..30116729 26863196 MeRIP-seq:(Medium) rs1328161024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2076405,Human_miRNA_ID_2076406,Human_miRNA_ID_2076407 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85090 RMVar_ID_85090 Human_SNP_ID_599429369 m1A Human chr16 - 30116693 30116693 30116693 GGAGCTCATCTTCCAGGAGACAGCACGCTTCCAGCCCGGAGTGCTGGAGGCCCCCTAGCCCAGAC GGAGCTCATCTTCCAGGAGACAGCACGCTTCCGGCCCGGAGTGCTGGAGGCCCCCTAGCCCAGAC T C MAPK3 Ensembl:ENSG00000102882 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30116626..30116775 26863196 MeRIP-seq:(Medium) rs754705731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817316,Human_RBP_ID_894032 Human_Splice_Rec_1702020,Human_Splice_Rec_1702021,Human_Splice_Rec_1702036,Human_Splice_Rec_1702037,Human_Splice_Rec_1702050,Human_Splice_Rec_1702051,Human_Splice_Rec_1702064,Human_Splice_Rec_1702065,Human_Splice_Rec_1702080,Human_Splice_Rec_1702081,Human_Splice_Rec_1702083,Human_Splice_Rec_1702088,Human_Splice_Rec_1702089,Human_Splice_Rec_1702096,Human_Splice_Rec_1702108,Human_Splice_Rec_1702120,Human_Splice_Rec_1702132 Human_miRNA_ID_171993 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_49841,RMVar_hsa_circ_66784,RMVar_hsa_circ_177848,RMVar_hsa_circ_177849 85091 RMVar_ID_85091 Human_SNP_ID_599429375 m1A Human chr16 - 30116701 30116701 30116701 CGGCTGAAGGAGCTCATCTTCCAGGAGACAGCACGCTTCCAGCCCGGAGTGCTGGAGGCCCCCTA CGGCTGAAGGAGCTCATCTTCCAGGAGACAGCCCGCTTCCAGCCCGGAGTGCTGGAGGCCCCCTA T G MAPK3 Ensembl:ENSG00000102882 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30116651..30116766 32194978 MeRIP-seq:(Medium) rs748781238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817316,Human_RBP_ID_894032,Human_RBP_ID_4362802 Human_Splice_Rec_1702020,Human_Splice_Rec_1702021,Human_Splice_Rec_1702036,Human_Splice_Rec_1702037,Human_Splice_Rec_1702050,Human_Splice_Rec_1702051,Human_Splice_Rec_1702064,Human_Splice_Rec_1702065,Human_Splice_Rec_1702080,Human_Splice_Rec_1702081,Human_Splice_Rec_1702083,Human_Splice_Rec_1702088,Human_Splice_Rec_1702089,Human_Splice_Rec_1702096,Human_Splice_Rec_1702108,Human_Splice_Rec_1702120,Human_Splice_Rec_1702132 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_49841,RMVar_hsa_circ_66784,RMVar_hsa_circ_177848,RMVar_hsa_circ_177849 85092 RMVar_ID_85092 Human_SNP_ID_599431181 m1A Human chr16 - 30123130 30123130 30123130 AACCGAGGGGGTCGGCCCGGGGGTCCCGGGGGAGGTGGAGATGGTGAAGGGGCAGCCGTTCGACG AACCGAGGGGGTCGGCCCGGGGGTCCCGGGGGGGGTGGAGATGGTGAAGGGGCAGCCGTTCGACG T C MAPK3 Ensembl:ENSG00000102882 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30123041..30123201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5754,Human_RBP_ID_233306,Human_RBP_ID_816965,Human_RBP_ID_888657,Human_RBP_ID_3947567,Human_RBP_ID_4362847,Human_RBP_ID_5113916,Human_RBP_ID_5141887,Human_RBP_ID_9419798,Human_RBP_ID_18419386,Human_RBP_ID_21973059,Human_RBP_ID_22441968,Human_RBP_ID_22584106,Human_RBP_ID_22654120,Human_RBP_ID_26328882,Human_RBP_ID_26769122,Human_RBP_ID_27811034 Human_Splice_Rec_1702007,Human_Splice_Rec_1702023,Human_Splice_Rec_1702053,Human_Splice_Rec_1702067,Human_Splice_Rec_1702097,Human_Splice_Rec_1702109,Human_Splice_Rec_1702133,Human_Splice_Rec_1702145 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 85093 RMVar_ID_85093 Human_SNP_ID_599431225 m1A Human chr16 + 30123192 30123189 30123193 GTTCTACGGGGCTCCCCGCCCCCGCCCCCCTGAGCCGCCGCCGCCGCCATCTCCACTCCTCCCCT GTTCTACGGGGCTCCCCGCCCCCGCCCCCC____CCGCCGCCGCCGCCATCTCCACTCCTCCCCT CTGAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr16:30123026..30123250;chr16:30123004..30123236 26863196 MeRIP-seq:(Medium) rs1336045165 Functional Loss DEL dbSNP153 31..34 33 - - - 85094 RMVar_ID_85094 Human_SNP_ID_599431228 m1A Human chr16 + 30123192 30123192 30123192 GTTCTACGGGGCTCCCCGCCCCCGCCCCCCTGAGCCGCCGCCGCCGCCATCTCCACTCCTCCCCT GTTCTACGGGGCTCCCCGCCCCCGCCCCCCTGTGCCGCCGCCGCCGCCATCTCCACTCCTCCCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr16:30123026..30123250;chr16:30123004..30123236 26863196 MeRIP-seq:(Medium) rs1415742359 Functional Loss SNV dbSNP153 33..33 33 - - - 85095 RMVar_ID_85095 Human_SNP_ID_599470307 m1A Human chr16 + 30335264 30335264 30335264 GAGCGGCGCGGTGAGAGAGGCGGATGAAGGCGAGGCGACGTCTCTTCCAGGGCCGTGCGCGGCCC GAGCGGCGCGGTGAGAGAGGCGGATGAAGGCGGGGCGACGTCTCTTCCAGGGCCGTGCGCGGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr16:30335223..30335324;chr16:30335218..30335341 26863196 MeRIP-seq:(Medium) rs1320613725 Functional Loss SNV dbSNP153 33..33 33 - - - 85096 RMVar_ID_85096 Human_SNP_ID_599474450 m1A Human chr16 - 30350996 30350996 30350996 ATGGGGGCCCTTATAAGGGAAGGGGAGTCACGAGGGTCTGCGCATGAAGCAAGGAAGCTTCTGGC ATGGGGGCCCTTATAAGGGAAGGGGAGTCACGGGGGTCTGCGCATGAAGCAAGGAAGCTTCTGGC T C CD2BP2 Ensembl:ENSG00000169217 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30350948..30351063 26863196 MeRIP-seq:(Medium) rs1029959735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277429,Human_RBP_ID_762864,Human_RBP_ID_5317517,Human_RBP_ID_6507611,Human_RBP_ID_18437509,Human_RBP_ID_26445049,Human_RBP_ID_27240398 85097 RMVar_ID_85097 Human_SNP_ID_599474466 m1A Human chr16 + 30351044 30351044 30351044 CTTATAAGGGCCCCCATGATTACTCAGGGCCCACCTCAACCATCCACGGTCATCTCCCCACCACG CTTATAAGGGCCCCCATGATTACTCAGGGCCCCCCTCAACCATCCACGGTCATCTCCCCACCACG A C lnc-MYLPF-3 RNACentral:URS00009B35BB lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30350897..30351163 26863196 MeRIP-seq:(Medium) rs1160027118 Functional Loss SNV dbSNP153 33..33 33 - - - 85098 RMVar_ID_85098 Human_SNP_ID_599475189 m1A Human chr16 - 30353252 30353252 30353252 CAGAGTCGCGGGGAGATGGTCTGGTGGATGTGATGTGGGAATATAAGTGGGAGAACACGGGGGAT CAGAGTCGCGGGGAGATGGTCTGGTGGATGTGGTGTGGGAATATAAGTGGGAGAACACGGGGGAT T C CD2BP2 Ensembl:ENSG00000169217 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30353201..30353300 26863196 MeRIP-seq:(Medium) rs780870231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762866,Human_RBP_ID_4363228,Human_RBP_ID_22945745,Human_RBP_ID_23686480,Human_RBP_ID_25205500 Human_Splice_Rec_1702740,Human_Splice_Rec_1702741,Human_Splice_Rec_1702750,Human_Splice_Rec_1702751 85099 RMVar_ID_85099 Human_SNP_ID_599475279 m1A Human chr16 + 30353427 30353427 30353427 CCAGTTCCTCCTCCGCCAACTCCTCAGCGAACATGTCCAGGGAGGGTGGGGGTGTGGGATTGTGG CCAGTTCCTCCTCCGCCAACTCCTCAGCGAACGTGTCCAGGGAGGGTGGGGGTGTGGGATTGTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr16:30353376..30353475;chr16:30353376..30353500 26863196,32194978 MeRIP-seq:(Medium) rs1398546550 Functional Loss SNV dbSNP153 33..33 33 - - - 85100 RMVar_ID_85100 Human_SNP_ID_599475406 m1A Human chr16 + 30353660 30353660 30353660 CCTCCTCGGGCCCCCAGACGCCTCAGTGCCCCAGCCACTGTCTCTCTAGGCAATAGGAGCTCCAA CCTCCTCGGGCCCCCAGACGCCTCAGTGCCCCCGCCACTGTCTCTCTAGGCAATAGGAGCTCCAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30352800..30354059 32194978 MeRIP-seq:(Medium) rs1180200406 Functional Loss SNV dbSNP153 33..33 33 - - - 85101 RMVar_ID_85101 Human_SNP_ID_599475592 m1A Human chr16 + 30354057 30354057 30354057 CCCCCCTCGCTGGGGAGTGTGGCTGCCTCCTGACCTGCACCAAAGACACAGGTGCCCTTTTCCAG CCCCCCTCGCTGGGGAGTGTGGCTGCCTCCTGCCCTGCACCAAAGACACAGGTGCCCTTTTCCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30353926..30354108 26863196 MeRIP-seq:(Medium) rs567323721 Functional Loss SNV dbSNP153 33..33 33 - - - 85102 RMVar_ID_85102 Human_SNP_ID_599475691 m1A Human chr16 - 30354252 30354252 30354252 CCGCTTTAAAGGCAAACACTCTTTGGATAGCGATGAGGAGGAGGATGATGATGATGGGGGGTCCA CCGCTTTAAAGGCAAACACTCTTTGGATAGCGCTGAGGAGGAGGATGATGATGATGGGGGGTCCA T G CD2BP2 Ensembl:ENSG00000169217 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30354201..30354325 26863196 MeRIP-seq:(Medium) rs755942758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1841327,Human_RBP_ID_3494139,Human_RBP_ID_4363258,Human_RBP_ID_6507657,Human_RBP_ID_12717577,Human_RBP_ID_17653381,Human_RBP_ID_18677547,Human_RBP_ID_22200183,Human_RBP_ID_23686484,Human_RBP_ID_24551917,Human_RBP_ID_25205511,Human_RBP_ID_26329988 Human_Splice_Rec_1702734,Human_Splice_Rec_1702735,Human_Splice_Rec_1702744,Human_Splice_Rec_1702745,Human_Splice_Rec_1702756 85103 RMVar_ID_85103 Human_SNP_ID_599475702 m1A Human chr16 - 30354275 30354275 30354275 GCTGGGTCAGGGGGTCCTGGGAGCCGCTTTAAAGGCAAACACTCTTTGGATAGCGATGAGGAGGA GCTGGGTCAGGGGGTCCTGGGAGCCGCTTTAAGGGCAAACACTCTTTGGATAGCGATGAGGAGGA T C CD2BP2 Ensembl:ENSG00000169217 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:30354183..30354331;chr16:30353951..30354725 26863196 MeRIP-seq:(Medium) rs377500973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12717578,Human_RBP_ID_17653381,Human_RBP_ID_17875317,Human_RBP_ID_24551917,Human_RBP_ID_26329988 Human_Splice_Rec_1702734,Human_Splice_Rec_1702735,Human_Splice_Rec_1702744,Human_Splice_Rec_1702745,Human_Splice_Rec_1702756 85104 RMVar_ID_85104 Human_SNP_ID_599477267 m1A Human chr16 - 30358485 30358485 30358485 CAAGAAGTGGCGGGAAACGCGGGGGGAGCTGCAGTATCGGCCCTCACGGCGACTGCATGGGTCCC CAAGAAGTGGCGGGAAACGCGGGGGGAGCTGCGGTATCGGCCCTCACGGCGACTGCATGGGTCCC T C TBC1D10B Ensembl:ENSG00000169221 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30358434..30358508 26863196 MeRIP-seq:(Medium) rs769218324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8806882,Human_RBP_ID_17875329,Human_RBP_ID_27240467 Human_Splice_Rec_1702760,Human_Splice_Rec_1702776,Human_Splice_Rec_1702788,Human_Splice_Rec_1702798 RMVar_hsa_circ_102223,RMVar_hsa_circ_121300,RMVar_hsa_circ_103789,RMVar_hsa_circ_177872,RMVar_hsa_circ_88798,RMVar_hsa_circ_91005,RMVar_hsa_circ_177874,RMVar_hsa_circ_82023,RMVar_hsa_circ_177873,RMVar_hsa_circ_177870,RMVar_hsa_circ_177871,RMVar_hsa_circ_177869 85105 RMVar_ID_85105 Human_SNP_ID_599478608 m1A Human chr16 - 30363141 30363132 30363141 AGAGGGGAGTAGGGTTTTTGGCCTGAGAAATGAGAAGAATGGAGTTGCTGTTTACTAATACAGAT AGAGGGGAGTAGGGTTTTTGGCCTGAGAAATG_________GAGTTGCTGTTTACTAATACAGAT CCATTCTTCT C TBC1D10B Ensembl:ENSG00000169221 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30363130..30363289 26863196 MeRIP-seq:(Medium) rs1165776907 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_12717695 RMVar_hsa_circ_103789,RMVar_hsa_circ_57718,RMVar_hsa_circ_82023,RMVar_hsa_circ_177870,RMVar_hsa_circ_177869 85106 RMVar_ID_85106 Human_SNP_ID_599479179 m1A Human chr16 - 30365499 30365499 30365499 TAACTGGGATAAGTGGCTGTCACGGCGATTCCAGAAGGTTTGAGGGCTGAATGGTGGGCAGGGCA TAACTGGGATAAGTGGCTGTCACGGCGATTCCGGAAGGTTTGAGGGCTGAATGGTGGGCAGGGCA T C TBC1D10B Ensembl:ENSG00000169221 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30365494..30365645 32194978 MeRIP-seq:(Medium) rs763542500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8806895,Human_RBP_ID_12717759 Human_Splice_Rec_1702762,Human_Splice_Rec_1702763,Human_Splice_Rec_1702777,Human_Splice_Rec_1702807 RMVar_hsa_circ_177875,RMVar_hsa_circ_98163 85107 RMVar_ID_85107 Human_SNP_ID_599480572 m1A Human chr16 - 30370348 30370348 30370348 TCGAGAGAGACCCCGGCGCGCGGCGCCCCCCGACCCCTGCCCCGCCTCTGCGCGCCCAGCGGCCG TCGAGAGAGACCCCGGCGCGCGGCGCCCCCCGCCCCCTGCCCCGCCTCTGCGCGCCCAGCGGCCG T G TBC1D10B Ensembl:ENSG00000169221 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEPG2 cell line,total RNA Untreated chr16:30370101..30370400;chr16:30370257..30370417 26863410,26863196 MeRIP-seq:(Medium) rs976655830 Functional Loss SNV dbSNP153 33..33 33 - - - 85108 RMVar_ID_85108 Human_SNP_ID_599480585 m1A Human chr16 - 30370371 30370371 30370371 AGCGCGCGAGGGGGTGAGAGGGCTCGAGAGAGACCCCGGCGCGCGGCGCCCCCCGACCCCTGCCC AGCGCGCGAGGGGGTGAGAGGGCTCGAGAGAGCCCCCGGCGCGCGGCGCCCCCCGACCCCTGCCC T G TBC1D10B Ensembl:ENSG00000169221 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30369963..30370493 26863196 MeRIP-seq:(Medium) rs929841484 Functional Loss SNV dbSNP153 33..33 33 - - - 85109 RMVar_ID_85109 Human_SNP_ID_599482723 m1A Human chr16 - 30378221 30378221 30378221 AGACACCGCCCACTTCCCGGCCCGGGGCCTGCACAATCTCCGACCGCATCACTGTCTTCCGGAGT AGACACCGCCCACTTCCCGGCCCGGGGCCTGCGCAATCTCCGACCGCATCACTGTCTTCCGGAGT T C SEPTIN1 Ensembl:ENSG00000180096 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30378181..30378339 26863196 MeRIP-seq:(Medium) rs931532839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472686,Human_RBP_ID_5128108,Human_RBP_ID_5464970 Human_miRNA_ID_629576,Human_miRNA_ID_1502572 85110 RMVar_ID_85110 Human_SNP_ID_599482795 m1A Human chr16 + 30378384 30378384 30378384 GCGCTGGGCAGTGTGGGGCGCGGGGATTGGACAAGAGGCCGACTGAAGGCGGAGCCGAGGTAAGG GCGCTGGGCAGTGTGGGGCGCGGGGATTGGACCAGAGGCCGACTGAAGGCGGAGCCGAGGTAAGG A C ZNF48 Ensembl:ENSG00000180035 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30378182..30378430 26863196 MeRIP-seq:(Medium) rs1181064379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1702863,Human_Splice_Rec_1702867 85111 RMVar_ID_85111 Human_SNP_ID_599489210 m1A Human chr16 + 30399136 30399136 30399136 ATGACGCGGTCCAGGGAGGGCGGAGGCCCAGGAGACCAAAGGGAGGGGCTCTGCCGCTTAGCAGA ATGACGCGGTCCAGGGAGGGCGGAGGCCCAGGTGACCAAAGGGAGGGGCTCTGCCGCTTAGCAGA A T ZNF48 Ensembl:ENSG00000180035 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30399009..30399285 26863196 MeRIP-seq:(Medium) rs997404885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2040899,Human_miRNA_ID_2193562,Human_miRNA_ID_2207772,Human_miRNA_ID_3019883,Human_miRNA_ID_3107712 RMVar_hsa_circ_77856,RMVar_hsa_circ_177877 85112 RMVar_ID_85112 Human_SNP_ID_599489213 m1A Human chr16 + 30399142 30399142 30399142 CGGTCCAGGGAGGGCGGAGGCCCAGGAGACCAAAGGGAGGGGCTCTGCCGCTTAGCAGAGAAGAA CGGTCCAGGGAGGGCGGAGGCCCAGGAGACCACAGGGAGGGGCTCTGCCGCTTAGCAGAGAAGAA A C ZNF48 Ensembl:ENSG00000180035 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30399042..30399165 26863196 MeRIP-seq:(Medium) rs769230301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_245710,Human_miRNA_ID_248218,Human_miRNA_ID_543895,Human_miRNA_ID_579128,Human_miRNA_ID_2193562,Human_miRNA_ID_2207772,Human_miRNA_ID_3107712 RMVar_hsa_circ_77856,RMVar_hsa_circ_177877 85113 RMVar_ID_85113 Human_SNP_ID_599491714 m1A Human chr16 - 30407663 30407663 30407663 CGGAAACCCCGGGGAGGGGGTGCGCACTCACCAGCCGAAGGTTCGGCACTCGCGGTGCCCCAGGC CGGAAACCCCGGGGAGGGGGTGCGCACTCACCCGCCGAAGGTTCGGCACTCGCGGTGCCCCAGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:30407625..30413604;chr16:30407576..30407953 26863196 MeRIP-seq:(Medium) rs1331091628 Functional Loss SNV dbSNP153 33..33 33 - - - 85114 RMVar_ID_85114 Human_SNP_ID_599492453 m1A Human chr16 + 30410510 30410509 30410510 GGATTGAAGACAAACGACTCAAGGCAGTGGGGAAGGCTTCCCAGAGGAGATGATTTTTGACTTGG GGATTGAAGACAAACGACTCAAGGCAGTGGGG_AGGCTTCCCAGAGGAGATGATTTTTGACTTGG GA G ZNF771 Ensembl:ENSG00000179965 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30410505..30410735 26863196 MeRIP-seq:(Medium) rs1214978433 Functional Loss DEL dbSNP153 33..33 33 - - - 85115 RMVar_ID_85115 Human_SNP_ID_599495953 m1A Human chr16 - 30424373 30424373 30424373 TGCCGCTAGCAGTGCTCTCCAAAATGGACATCAACCGGCGACGCTACCCAGCCCATCTGGCCCGC TGCCGCTAGCAGTGCTCTCCAAAATGGACATCGACCGGCGACGCTACCCAGCCCATCTGGCCCGC T C DCTPP1 Ensembl:ENSG00000179958 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30424322..30424481 26863196 MeRIP-seq:(Medium) rs1401805447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472736,Human_RBP_ID_1004079,Human_RBP_ID_1516652,Human_RBP_ID_1841364,Human_RBP_ID_4363612,Human_RBP_ID_12718415,Human_RBP_ID_17253927,Human_RBP_ID_17369493,Human_RBP_ID_17486085,Human_RBP_ID_27240549 Human_Splice_Rec_1703036 RMVar_hsa_circ_80015,RMVar_hsa_circ_122935,RMVar_hsa_circ_177879,RMVar_hsa_circ_177880 85116 RMVar_ID_85116 Human_SNP_ID_599495966 m1A Human chr16 - 30424408 30424408 30424408 CCTGGTGGCATTAGCAGCCCGCTGCCGTGTGGATCTGCCGCTAGCAGTGCTCTCCAAAATGGACA CCTGGTGGCATTAGCAGCCCGCTGCCGTGTGGCTCTGCCGCTAGCAGTGCTCTCCAAAATGGACA T G DCTPP1 Ensembl:ENSG00000179958 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:30424359..30424458;chr16:30424161..30424409 32194978 MeRIP-seq:(Medium) rs773589795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472738,Human_RBP_ID_1516652,Human_RBP_ID_17875386,Human_RBP_ID_22441970,Human_RBP_ID_22801063,Human_RBP_ID_23686573,Human_RBP_ID_26810289,Human_RBP_ID_27240550 Human_Splice_Rec_1703036 RMVar_hsa_circ_80015,RMVar_hsa_circ_122935,RMVar_hsa_circ_177879,RMVar_hsa_circ_177880 85117 RMVar_ID_85117 Human_SNP_ID_599497396 m1A Human chr16 + 30429859 30429848 30429860 ACGCGGGAGAAAGGGGCGACTTCCCCACCCCGAGCTGGGCCAGGCCTGCTTACATGTCCTCGAGC ACGCGGGAGAAAGGGGCGACTT____________CTGGGCCAGGCCTGCTTACATGTCCTCGAGC TCCCCACCCCGAG T ZNF771 Ensembl:ENSG00000179965 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30429853..30430011 26863410 MeRIP-seq:(Medium) rs532394112 Functional Loss DEL dbSNP153 23..34 33 - - - 85118 RMVar_ID_85118 Human_SNP_ID_599497464 m1A Human chr16 + 30429966 30429966 30429966 TCCTCTCCCCCCGTGTCCCCACGAATCTCCCCACCGGCCACAGACATGCCGCCCACCGCTGCACC TCCTCTCCCCCCGTGTCCCCACGAATCTCCCCCCCGGCCACAGACATGCCGCCCACCGCTGCACC A C ZNF771 Ensembl:ENSG00000179965 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30429813..30430025 26863196 MeRIP-seq:(Medium) rs767784123 Functional Loss SNV dbSNP153 33..33 33 - - - 85119 RMVar_ID_85119 Human_SNP_ID_599501012 m1A Human chr16 + 30444459 30444459 30444459 ACAGCAGCTGTGGCCCCACGAGGCAGGACTTCAATAACTCGCGGCTTGTCAATGATCCGGGCCGT ACAGCAGCTGTGGCCCCACGAGGCAGGACTTCTATAACTCGCGGCTTGTCAATGATCCGGGCCGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30444408..30444551 26863196 MeRIP-seq:(Medium) rs1473027549 Functional Loss SNV dbSNP153 33..33 33 - - - 85120 RMVar_ID_85120 Human_SNP_ID_599501512 m1A Human chr16 - 30445768 30445767 30445768 TTTGCTTCATATTAATCTGAGTGGAAAATAAAAGGGCCCTCTTCTCCTCTCGCTTCCCTGCCGGG TTTGCTTCATATTAATCTGAGTGGAAAATAAA_GGGCCCTCTTCTCCTCTCGCTTCCCTGCCGGG CT C SEPHS2 Ensembl:ENSG00000179918 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30445655..30445801 26863196 MeRIP-seq:(Medium) rs1413104022 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1281771,Human_RBP_ID_4393759,Human_RBP_ID_5440410,Human_RBP_ID_5464979,Human_RBP_ID_9325070,Human_RBP_ID_26942951 85121 RMVar_ID_85121 Human_SNP_ID_599522470 m1A Human chr16 + 30525126 30525126 30525126 TGTGGGCACTTGTAGGGCTTCTGGCCAGAGTGAGTGCGCTGGTGGCGAAGCAGGTAAGAGCTGTC TGTGGGCACTTGTAGGGCTTCTGGCCAGAGTGCGTGCGCTGGTGGCGAAGCAGGTAAGAGCTGTC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30525027..30525151 26863196 MeRIP-seq:(Medium) rs1219976650 Functional Loss SNV dbSNP153 33..33 33 - - - 85122 RMVar_ID_85122 Human_SNP_ID_599522471 m1A Human chr16 + 30525126 30525126 30525126 TGTGGGCACTTGTAGGGCTTCTGGCCAGAGTGAGTGCGCTGGTGGCGAAGCAGGTAAGAGCTGTC TGTGGGCACTTGTAGGGCTTCTGGCCAGAGTGGGTGCGCTGGTGGCGAAGCAGGTAAGAGCTGTC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30525027..30525151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 85123 RMVar_ID_85123 Human_SNP_ID_599522968 m1A Human chr16 - 30526347 30526345 30526348 CCCAGGATGTGCAGAGTTCTGACGAAATGAGGAGCCCCGAAGGGTACCTCAGAGGTGAGGAGGGA CCCAGGATGTGCAGAGTTCTGACGAAATGAG___CCCCGAAGGGTACCTCAGAGGTGAGGAGGGA GCTC G AC002310.4,ZNF768 Ensembl:ENSG00000261459,Ensembl:ENSG00000169957 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30524399..30532345 32194978 MeRIP-seq:(Medium) rs752073679 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1516727,Human_RBP_ID_1841399,Human_RBP_ID_4393761,Human_RBP_ID_5142220,Human_RBP_ID_5317521,Human_RBP_ID_8186955,Human_RBP_ID_8941339,Human_RBP_ID_9325957,Human_RBP_ID_12718577,Human_RBP_ID_18677642,Human_RBP_ID_22053141,Human_RBP_ID_23686631,Human_RBP_ID_26943007 Human_Splice_Rec_1703305 85124 RMVar_ID_85124 Human_SNP_ID_599522995 m1A Human chr16 - 30526403 30526403 30526403 GCTGCACTGGGAGCCCGCGGGGATGGAGCGGGAGGCGTTGCCGTGGGGCCTCGAGCCCCAGGATG GCTGCACTGGGAGCCCGCGGGGATGGAGCGGGCGGCGTTGCCGTGGGGCCTCGAGCCCCAGGATG T G AC002310.4,ZNF768 Ensembl:ENSG00000261459,Ensembl:ENSG00000169957 Protein coding,Protein coding intron,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs373129815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234514,Human_RBP_ID_3502684,Human_RBP_ID_3947571,Human_RBP_ID_4393019,Human_RBP_ID_5113925,Human_RBP_ID_5142781,Human_RBP_ID_5316644,Human_RBP_ID_5495510,Human_RBP_ID_8186955,Human_RBP_ID_8811867,Human_RBP_ID_8941339,Human_RBP_ID_9325072,Human_RBP_ID_9419803,Human_RBP_ID_18940201,Human_RBP_ID_21971235,Human_RBP_ID_22053141,Human_RBP_ID_22497742,Human_RBP_ID_23686633 Human_Splice_Rec_1703305 85125 RMVar_ID_85125 Human_SNP_ID_599523013 m1A Human chr16 + 30526446 30526441 30526447 CCCCGCGGGCTCCCAGTGCAGCGGCGGCGGCGATGGCGGCCGATCCCGCGACCCGGCCTCGGTTG CCCCGCGGGCTCCCAGTGCAGCGGCGGC______GGCGGCCGATCCCGCGACCCGGCCTCGGTTG CGGCGAT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr16:30526336..30526747;chr16:30526351..30526500 26863196,26863410 MeRIP-seq:(Medium) rs1353860350 Functional Loss DEL dbSNP153 29..34 33 - - - 85126 RMVar_ID_85126 Human_SNP_ID_599523028 m1A Human chr16 + 30526464 30526464 30526464 CAGCGGCGGCGGCGATGGCGGCCGATCCCGCGACCCGGCCTCGGTTGCCCCGAGCCGCGGGCCCC CAGCGGCGGCGGCGATGGCGGCCGATCCCGCGCCCCGGCCTCGGTTGCCCCGAGCCGCGGGCCCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr16:30526326..30526766;chr16:30526326..30526724 26863196,26863410 MeRIP-seq:(Medium) rs778129091 Functional Loss SNV dbSNP153 33..33 33 - - - 85127 RMVar_ID_85127 Human_SNP_ID_599523072 m1A Human chr16 - 30526566 30526566 30526566 GGGGCCCGGCGCGCTGGAGAGGCGCGGGGTCAAGACGTCCGGCCTCGGGGGCCCGGGCTGGGCCG GGGGCCCGGCGCGCTGGAGAGGCGCGGGGTCAGGACGTCCGGCCTCGGGGGCCCGGGCTGGGCCG T C AC002310.4,ZNF768 Ensembl:ENSG00000261459,Ensembl:ENSG00000169957 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972533,GSM1972534 HEK293T,H2O2 treatment;HEPG2 cell line,total RNA Untreated chr16:30526469..30526569;chr16:30526526..30526750 26863410,26863196 MeRIP-seq:(Medium) rs1266302485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235105,Human_RBP_ID_472803,Human_RBP_ID_1004109,Human_RBP_ID_3502686,Human_RBP_ID_4393021,Human_RBP_ID_5141897,Human_RBP_ID_5316645,Human_RBP_ID_8184513,Human_RBP_ID_9325073,Human_RBP_ID_9353115,Human_RBP_ID_9419189,Human_RBP_ID_17669668,Human_RBP_ID_18418991,Human_RBP_ID_22714335,Human_RBP_ID_26779694 85128 RMVar_ID_85128 Human_SNP_ID_599531948 m1A Human chr16 - 30558070 30558068 30558070 CTTCGCGGACGTGGCCGTGTACTTCTGCCGGGAGGAGTGGGGCTGCTTGCGGCCAGCGCAGAGGG CTTCGCGGACGTGGCCGTGTACTTCTGCCGGG__GAGTGGGGCTGCTTGCGGCCAGCGCAGAGGG CCT C ZNF764 Ensembl:ENSG00000169951 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30557906..30558075 26863196 MeRIP-seq:(Medium) rs1370604807 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_763092,Human_RBP_ID_6507963,Human_RBP_ID_9374186,Human_RBP_ID_22049841,Human_RBP_ID_27560060 Human_Splice_Rec_1703329,Human_Splice_Rec_1703333 85129 RMVar_ID_85129 Human_SNP_ID_599532055 m1A Human chr16 - 30558222 30558222 30558222 GCGCAGGAGGTTCCGCAGGCCCAGGCCAGGCCAGGGGAGGCAGCCGATCCGTCGTCGGGGTTGAC GCGCAGGAGGTTCCGCAGGCCCAGGCCAGGCCGGGGGAGGCAGCCGATCCGTCGTCGGGGTTGAC T C ZNF764 Ensembl:ENSG00000169951 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30558174..30558371 26863196 MeRIP-seq:(Medium) rs1270602356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762885,Human_RBP_ID_4364052,Human_RBP_ID_5142785,Human_RBP_ID_17875466 85130 RMVar_ID_85130 Human_SNP_ID_599535158 m1A Human chr16 - 30570263 30570263 30570263 CACAGCCACCCAAAAATGCTGCCTGGGACCCGACCACAGGAGCACAGCCCCCGGCACCCATACCC CACAGCCACCCAAAAATGCTGCCTGGGACCCGGCCACAGGAGCACAGCCCCCGGCACCCATACCC T C ZNF688 Ensembl:ENSG00000229809 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30570181..30570277 26863410 MeRIP-seq:(Medium) rs771164003 Functional Loss SNV dbSNP153 33..33 33 - - - 85131 RMVar_ID_85131 Human_SNP_ID_599539392 m1A Human chr16 - 30585623 30585623 30585623 ACCTTCCCCGGAAGCCTCCCTTTGCCAGGCAGAAAGGGTTTCCCATGGGGCCGCCCCTGGCGCCG ACCTTCCCCGGAAGCCTCCCTTTGCCAGGCAGTAAGGGTTTCCCATGGGGCCGCCCCTGGCGCCG T A ZNF785 Ensembl:ENSG00000197162 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30585572..30585735 26863196 MeRIP-seq:(Medium) rs1339035091 Functional Loss SNV dbSNP153 33..33 33 - - - 85132 RMVar_ID_85132 Human_SNP_ID_599556247 m1A Human chr16 + 30651630 30651630 30651630 CGCAGCCTGGGATTCCCCAGGGACCCCCCCGGAGCCGCCGCGTCTCCCATGGACTTGCCCGGGGA CGCAGCCTGGGATTCCCCAGGGACCCCCCCGGCGCCGCCGCGTCTCCCATGGACTTGCCCGGGGA A C PRR14 Ensembl:ENSG00000156858 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30651580..30651730 32194978 MeRIP-seq:(Medium) rs759410335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888662,Human_RBP_ID_22582415 Human_Splice_Rec_1703414,Human_Splice_Rec_1703415,Human_Splice_Rec_1703420,Human_Splice_Rec_1703421,Human_Splice_Rec_1703434,Human_Splice_Rec_1703435,Human_Splice_Rec_1703442,Human_Splice_Rec_1703443,Human_Splice_Rec_1703448,Human_Splice_Rec_1703466,Human_Splice_Rec_1703467,Human_Splice_Rec_1703488,Human_Splice_Rec_1703489,Human_Splice_Rec_1703494,Human_Splice_Rec_1703495,Human_Splice_Rec_1703513 RMVar_hsa_circ_101127,RMVar_hsa_circ_117914,RMVar_hsa_circ_177902,RMVar_hsa_circ_177903 85133 RMVar_ID_85133 Human_SNP_ID_599556248 m1A Human chr16 + 30651630 30651630 30651630 CGCAGCCTGGGATTCCCCAGGGACCCCCCCGGAGCCGCCGCGTCTCCCATGGACTTGCCCGGGGA CGCAGCCTGGGATTCCCCAGGGACCCCCCCGGGGCCGCCGCGTCTCCCATGGACTTGCCCGGGGA A G PRR14 Ensembl:ENSG00000156858 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30651580..30651730 32194978 MeRIP-seq:(Medium) rs759410335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888662,Human_RBP_ID_22582415 Human_Splice_Rec_1703414,Human_Splice_Rec_1703415,Human_Splice_Rec_1703420,Human_Splice_Rec_1703421,Human_Splice_Rec_1703434,Human_Splice_Rec_1703435,Human_Splice_Rec_1703442,Human_Splice_Rec_1703443,Human_Splice_Rec_1703448,Human_Splice_Rec_1703466,Human_Splice_Rec_1703467,Human_Splice_Rec_1703488,Human_Splice_Rec_1703489,Human_Splice_Rec_1703494,Human_Splice_Rec_1703495,Human_Splice_Rec_1703513 RMVar_hsa_circ_101127,RMVar_hsa_circ_117914,RMVar_hsa_circ_177902,RMVar_hsa_circ_177903 85134 RMVar_ID_85134 Human_SNP_ID_599557279 m1A Human chr16 - 30654723 30654723 30654723 TCAGCAAAGCTCTCCAGCTTGGAGCGGACGGAACGGAAGAGCGGGGCCAAGCCCCAGGGACTGAG TCAGCAAAGCTCTCCAGCTTGGAGCGGACGGAGCGGAAGAGCGGGGCCAAGCCCCAGGGACTGAG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:30654606..30654763 26863410 MeRIP-seq:(Medium) rs1228277715 Functional Loss SNV dbSNP153 33..33 33 - - - 85135 RMVar_ID_85135 Human_SNP_ID_599557332 m1A Human chr16 + 30654808 30654808 30654808 AAACCCCACAGCCCCCACCCCCGTCCCCCCCAATGAAGCTGGAGTTGAAGATCGCCATCTCAGAG AAACCCCACAGCCCCCACCCCCGTCCCCCCCACTGAAGCTGGAGTTGAAGATCGCCATCTCAGAG A C PRR14 Ensembl:ENSG00000156858 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30654626..30654881 26863196 MeRIP-seq:(Medium) rs140826259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472876,Human_RBP_ID_5128594,Human_RBP_ID_17077472 RMVar_hsa_circ_83847,RMVar_hsa_circ_117914,RMVar_hsa_circ_177903,RMVar_hsa_circ_177905,RMVar_hsa_circ_62512,RMVar_hsa_circ_177904,RMVar_hsa_circ_372460,RMVar_hsa_circ_121285,RMVar_hsa_circ_177906,RMVar_hsa_circ_93669,RMVar_hsa_circ_177909,RMVar_hsa_circ_82503,RMVar_hsa_circ_103261,RMVar_hsa_circ_177910,RMVar_hsa_circ_177912 85136 RMVar_ID_85136 Human_SNP_ID_599557333 m1A Human chr16 + 30654808 30654808 30654808 AAACCCCACAGCCCCCACCCCCGTCCCCCCCAATGAAGCTGGAGTTGAAGATCGCCATCTCAGAG AAACCCCACAGCCCCCACCCCCGTCCCCCCCAGTGAAGCTGGAGTTGAAGATCGCCATCTCAGAG A G PRR14 Ensembl:ENSG00000156858 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30654626..30654881 26863196 MeRIP-seq:(Medium) rs140826259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472876,Human_RBP_ID_5128594,Human_RBP_ID_17077472 RMVar_hsa_circ_83847,RMVar_hsa_circ_117914,RMVar_hsa_circ_177903,RMVar_hsa_circ_177905,RMVar_hsa_circ_62512,RMVar_hsa_circ_177904,RMVar_hsa_circ_372460,RMVar_hsa_circ_121285,RMVar_hsa_circ_177906,RMVar_hsa_circ_93669,RMVar_hsa_circ_177909,RMVar_hsa_circ_82503,RMVar_hsa_circ_103261,RMVar_hsa_circ_177910,RMVar_hsa_circ_177912 85137 RMVar_ID_85137 Human_SNP_ID_599557438 m1A Human chr16 - 30655076 30655076 30655076 GACAGGGCCGAGGGGGTGGCGGGGCTCGGGCCATTTCCCCACCACCCACAGTGTGCCGCCGCGGC GACAGGGCCGAGGGGGTGGCGGGGCTCGGGCCGTTTCCCCACCACCCACAGTGTGCCGCCGCGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30655051..30655200 26863196 MeRIP-seq:(Medium) rs1238108144 Functional Loss SNV dbSNP153 33..33 33 - - - 85138 RMVar_ID_85138 Human_SNP_ID_599558644 m1A Human chr16 - 30658570 30658570 30658570 CCTCCGTCTCTGTCCGACTTGGGCCTTAGGGGATCCGGAACGGCCGATGGGCAGCGGGGGAGCTC CCTCCGTCTCTGTCCGACTTGGGCCTTAGGGGCTCCGGAACGGCCGATGGGCAGCGGGGGAGCTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30658456..30658601 26863196 MeRIP-seq:(Medium) rs553063564 Functional Loss SNV dbSNP153 33..33 33 - - - 85139 RMVar_ID_85139 Human_SNP_ID_599559229 m1A Human chr16 + 30659777 30659777 30659777 CTGGGGGCCCGAGACGCCGGCGGCCCCGTCCGAGACCTCGACCCCCGCGACCCCGAGCTCGGAAG CTGGGGGCCCGAGACGCCGGCGGCCCCGTCCGCGACCTCGACCCCCGCGACCCCGAGCTCGGAAG A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr16:30659735..30659925;chr16:30659077..30660458 26863196 MeRIP-seq:(Medium) rs1341215808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762701 85140 RMVar_ID_85140 Human_SNP_ID_599559316 m1A Human chr16 + 30659889 30659889 30659889 GGAGGAGGGGGGCGCAGACGACGGCGAAGCCGAGGAGGAGCCTGAGGAGGAGGAAGAGGAGGAGG GGAGGAGGGGGGCGCAGACGACGGCGAAGCCGGGGAGGAGCCTGAGGAGGAGGAAGAGGAGGAGG A G FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:30659177..30660309;chr16:30659136..30659977 26863196 MeRIP-seq:(Medium) rs951667158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9285755 Human_Splice_Rec_1703549,Human_Splice_Rec_1703583,Human_Splice_Rec_1703585,Human_Splice_Rec_1703603 85141 RMVar_ID_85141 Human_SNP_ID_599559317 m1A Human chr16 + 30659889 30659889 30659889 GGAGGAGGGGGGCGCAGACGACGGCGAAGCCGAGGAGGAGCCTGAGGAGGAGGAAGAGGAGGAGG GGAGGAGGGGGGCGCAGACGACGGCGAAGCCGTGGAGGAGCCTGAGGAGGAGGAAGAGGAGGAGG A T FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:30659177..30660309;chr16:30659136..30659977 26863196 MeRIP-seq:(Medium) rs951667158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9285755 Human_Splice_Rec_1703549,Human_Splice_Rec_1703583,Human_Splice_Rec_1703585,Human_Splice_Rec_1703603 85142 RMVar_ID_85142 Human_SNP_ID_599559490 m1A Human chr16 - 30660316 30660316 30660316 GCCCCACTGGAGCCCCCCCTTTTCCGCTTCCCAGAATGCTTCAGCCGATGTTCCAGTCGCTCTGG GCCCCACTGGAGCCCCCCCTTTTCCGCTTCCCTGAATGCTTCAGCCGATGTTCCAGTCGCTCTGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30660247..30660401 26863196 MeRIP-seq:(Medium) rs972579734 Functional Loss SNV dbSNP153 33..33 33 - - - 85143 RMVar_ID_85143 Human_SNP_ID_599559491 m1A Human chr16 - 30660316 30660316 30660316 GCCCCACTGGAGCCCCCCCTTTTCCGCTTCCCAGAATGCTTCAGCCGATGTTCCAGTCGCTCTGG GCCCCACTGGAGCCCCCCCTTTTCCGCTTCCCCGAATGCTTCAGCCGATGTTCCAGTCGCTCTGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30660247..30660401 26863196 MeRIP-seq:(Medium) rs972579734 Functional Loss SNV dbSNP153 33..33 33 - - - 85144 RMVar_ID_85144 Human_SNP_ID_599559701 m1A Human chr16 - 30660930 30660930 30660930 TCCCCGTGTCTTTTCTTAGCAAACTTCTGACTATACTTCAGGACCTGACTAAGACATCCTAGGGG TCCCCGTGTCTTTTCTTAGCAAACTTCTGACTCTACTTCAGGACCTGACTAAGACATCCTAGGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30660925..30661078 26863196 MeRIP-seq:(Medium) rs1000762037 Functional Loss SNV dbSNP153 33..33 33 - - - 85145 RMVar_ID_85145 Human_SNP_ID_599560267 m1A Human chr16 + 30662664 30662664 30662664 GGAGCGGAGCCAAGAACAGCCCCCGGGGCCCGACCCGCTGCTAGTGCCTTTCCCCCCAAAGGAAC GGAGCGGAGCCAAGAACAGCCCCCGGGGCCCGCCCCGCTGCTAGTGCCTTTCCCCCCAAAGGAAC A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30662551..30662765 26863196 MeRIP-seq:(Medium) rs1335757393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761600,Human_RBP_ID_817413,Human_RBP_ID_27441625 Human_miRNA_ID_1964637,Human_miRNA_ID_2650387,Human_miRNA_ID_2652339,Human_miRNA_ID_2756912,Human_miRNA_ID_2764089 RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915 85146 RMVar_ID_85146 Human_SNP_ID_599560284 m1A Human chr16 + 30662691 30662691 30662691 GCCCGACCCGCTGCTAGTGCCTTTCCCCCCAAAGGAACCACCGCCTCCACCGGTCCCTCGGCCTC GCCCGACCCGCTGCTAGTGCCTTTCCCCCCAAGGGAACCACCGCCTCCACCGGTCCCTCGGCCTC A G FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr16:30662551..30662818;chr16:30662651..30662800 26863196 MeRIP-seq:(Medium) rs1181839271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128597,Human_RBP_ID_26943208,Human_RBP_ID_27441625 RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915 85147 RMVar_ID_85147 Human_SNP_ID_599560300 m1A Human chr16 - 30662712 30662712 30662712 GGGGTGCAGGGGGTGAGACAGGAGGCCGAGGGACCGGTGGAGGCGGTGGTTCCTTTGGGGGGAAA GGGGTGCAGGGGGTGAGACAGGAGGCCGAGGGGCCGGTGGAGGCGGTGGTTCCTTTGGGGGGAAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:30662664..30662850 26863196 MeRIP-seq:(Medium) rs1378470784 Functional Loss SNV dbSNP153 33..33 33 - - - 85148 RMVar_ID_85148 Human_SNP_ID_599560318 m1A Human chr16 + 30662740 30662740 30662740 CCGGTCCCTCGGCCTCCTGTCTCACCCCCTGCACCCCTGCCGGCCACTCCCAGTCTGCCACCCCC CCGGTCCCTCGGCCTCCTGTCTCACCCCCTGCCCCCCTGCCGGCCACTCCCAGTCTGCCACCCCC A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30662484..30665362 26863196 MeRIP-seq:(Medium) rs1024401908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761601,Human_RBP_ID_5128598,Human_RBP_ID_17371418,Human_RBP_ID_18939021,Human_RBP_ID_22532703,Human_RBP_ID_27441626 RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915 85149 RMVar_ID_85149 Human_SNP_ID_599560854 m1A Human chr16 - 30664364 30664364 30664364 GCAGCCCGGGAGGGGGAAAGCTGTGGGTGGACAAAGGCAGGGGCAGTGAGGGCGTCGGGGGCCGG GCAGCCCGGGAGGGGGAAAGCTGTGGGTGGACGAAGGCAGGGGCAGTGAGGGCGTCGGGGGCCGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:30664276..30664426 26863410 MeRIP-seq:(Medium) rs1248329555 Functional Loss SNV dbSNP153 33..33 33 - - - 85150 RMVar_ID_85150 Human_SNP_ID_599560893 m1A Human chr16 + 30664418 30664418 30664418 TCCCGGGCTGCGGCCCCCCCCACCACCCCACCACCCCTCCTTGTTCTCCCCTGGCCCCACCCTGC TCCCGGGCTGCGGCCCCCCCCACCACCCCACCCCCCCTCCTTGTTCTCCCCTGGCCCCACCCTGC A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:30664331..30664513 26863196 MeRIP-seq:(Medium) rs1230417859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17078676 Human_Splice_Rec_1703561,Human_Splice_Rec_1703615 RMVar_hsa_circ_5600,RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915,RMVar_hsa_circ_338639,RMVar_hsa_circ_177918 85151 RMVar_ID_85151 Human_SNP_ID_599561367 m1A Human chr16 + 30665644 30665644 30665644 CTGATCCCTCCACTCCCCTTTCCCAGAGCACGAACCCTGAGCTGCCACCACGACTGGGGCCGGTG CTGATCCCTCCACTCCCCTTTCCCAGAGCACGTACCCTGAGCTGCCACCACGACTGGGGCCGGTG A T FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30665311..30666065 32194978 MeRIP-seq:(Medium) rs1212856115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8806993,Human_RBP_ID_17371421 Human_Splice_Rec_1703568,Human_Splice_Rec_1703569,Human_Splice_Rec_1703622,Human_Splice_Rec_1703623 RMVar_hsa_circ_5600,RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915,RMVar_hsa_circ_338639,RMVar_hsa_circ_11729,RMVar_hsa_circ_177918 85152 RMVar_ID_85152 Human_SNP_ID_599562493 m1A Human chr16 - 30668954 30668954 30668954 GGCACACCTGTCCTTCTCCTCCTTGGTGATGGAGGGCTCCCTCCGCTCCACAGGCCGCTCCTTGT GGCACACCTGTCCTTCTCCTCCTTGGTGATGGTGGGCTCCCTCCGCTCCACAGGCCGCTCCTTGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30668783..30669420 32194978 MeRIP-seq:(Medium) rs753001934 Functional Loss SNV dbSNP153 33..33 33 - - - 85153 RMVar_ID_85153 Human_SNP_ID_599562494 m1A Human chr16 - 30668954 30668954 30668954 GGCACACCTGTCCTTCTCCTCCTTGGTGATGGAGGGCTCCCTCCGCTCCACAGGCCGCTCCTTGT GGCACACCTGTCCTTCTCCTCCTTGGTGATGGGGGGCTCCCTCCGCTCCACAGGCCGCTCCTTGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30668783..30669420 32194978 MeRIP-seq:(Medium) rs753001934 Functional Loss SNV dbSNP153 33..33 33 - - - 85154 RMVar_ID_85154 Human_SNP_ID_599562617 m1A Human chr16 + 30669191 30669191 30669191 ATCTGTGCGGGTAAAGGAAGAGCGGAAGGAGGAGGCTGCCGCCGCCGCTGCCGCTGCTGCTGCCG ATCTGTGCGGGTAAAGGAAGAGCGGAAGGAGGCGGCTGCCGCCGCCGCTGCCGCTGCTGCTGCCG A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30669141..30669261 26863196 MeRIP-seq:(Medium) rs1419725463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233865,Human_RBP_ID_894238,Human_RBP_ID_5114219,Human_RBP_ID_8231066,Human_RBP_ID_18469738 RMVar_hsa_circ_85133,RMVar_hsa_circ_177915 85155 RMVar_ID_85155 Human_SNP_ID_599562618 m1A Human chr16 + 30669191 30669191 30669191 ATCTGTGCGGGTAAAGGAAGAGCGGAAGGAGGAGGCTGCCGCCGCCGCTGCCGCTGCTGCTGCCG ATCTGTGCGGGTAAAGGAAGAGCGGAAGGAGGGGGCTGCCGCCGCCGCTGCCGCTGCTGCTGCCG A G FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30669141..30669261 26863196 MeRIP-seq:(Medium) rs1419725463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233865,Human_RBP_ID_894238,Human_RBP_ID_5114219,Human_RBP_ID_8231066,Human_RBP_ID_18469738 RMVar_hsa_circ_85133,RMVar_hsa_circ_177915 85156 RMVar_ID_85156 Human_SNP_ID_599562823 m1A Human chr16 - 30669507 30669507 30669507 CTGAGAAGGTGAGGGGTTCCCGGGGCCGCAGCAGGTGGTGGTGGAGGAGCCAAGCGGCTGTAGAG CTGAGAAGGTGAGGGGTTCCCGGGGCCGCAGCTGGTGGTGGTGGAGGAGCCAAGCGGCTGTAGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30669457..30669580 26863196 MeRIP-seq:(Medium) rs985411167 Functional Loss SNV dbSNP153 33..33 33 - - - 85157 RMVar_ID_85157 Human_SNP_ID_599562875 m1A Human chr16 + 30669627 30669627 30669627 CGGCCCAGTTCCCCACCTAGGGGCCCTGGCCCAGCTCGGGCTGACAGGTGAGGGGAACGGGGGGG CGGCCCAGTTCCCCACCTAGGGGCCCTGGCCCTGCTCGGGCTGACAGGTGAGGGGAACGGGGGGG A T FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30669526..30669769 26863410 MeRIP-seq:(Medium) rs754286168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2663025,Human_miRNA_ID_2681476 RMVar_hsa_circ_85133,RMVar_hsa_circ_177915 85158 RMVar_ID_85158 Human_SNP_ID_599571105 m1A Human chr16 - 30698237 30698237 30698237 CAGCGAACCGCCGCTGCCGCTCCCGAGGCCTCACCAAAATGGCCGCCGCCGTCTCGGCCGCCACC CAGCGAACCGCCGCTGCCGCTCCCGAGGCCTCCCCAAAATGGCCGCCGCCGTCTCGGCCGCCACC T G AC093249.6 Ensembl:ENSG00000261840 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30698190..30698360 26863196 MeRIP-seq:(Medium) rs1207280498 Functional Loss SNV dbSNP153 33..33 33 - - - 85159 RMVar_ID_85159 Human_SNP_ID_599571128 m1A Human chr16 + 30698272 30698272 30698272 GGCCTCGGGAGCGGCAGCGGCGGTTCGCTGGGAGTAGCGTCTGCCCTTTTTCCCACCCACCGTCC GGCCTCGGGAGCGGCAGCGGCGGTTCGCTGGGCGTAGCGTCTGCCCTTTTTCCCACCCACCGTCC A C SRCAP Ensembl:ENSG00000080603 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30698226..30698388 26863196 MeRIP-seq:(Medium) rs1464966259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4364467,Human_RBP_ID_18418716,Human_RBP_ID_27837832 85160 RMVar_ID_85160 Human_SNP_ID_599571226 m1A Human chr16 + 30698456 30698456 30698456 CGGGAGGGGGGGTGGTGCGCACGCCCCCGAGGACGCAGGTAAGGAGAGGGAGACAAGATGGCGAA CGGGAGGGGGGGTGGTGCGCACGCCCCCGAGGTCGCAGGTAAGGAGAGGGAGACAAGATGGCGAA A T SRCAP Ensembl:ENSG00000080603 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30698359..30698509 26863410 MeRIP-seq:(Medium) rs1045121286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1703657 85161 RMVar_ID_85161 Human_SNP_ID_599571369 m1A Human chr16 - 30698701 30698701 30698701 CTCGCTCGCTCGCTCAGGCACGCGTGCGCAGAAGGGCGGGAAGGGAGAGGAGACACGCCGGGGCC CTCGCTCGCTCGCTCAGGCACGCGTGCGCAGACGGGCGGGAAGGGAGAGGAGACACGCCGGGGCC T G AC093249.6 Ensembl:ENSG00000261840 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30698651..30698797 26863196 MeRIP-seq:(Medium) rs1457201863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393028 85162 RMVar_ID_85162 Human_SNP_ID_599571605 m1A Human chr16 + 30699169 30699169 30699169 TGGCAACTTGGGCAGAGGTCAGGGGTCACGCGAGGTCAGTCCGTCGGGAGGGCTAGGGAGATGGT TGGCAACTTGGGCAGAGGTCAGGGGTCACGCGCGGTCAGTCCGTCGGGAGGGCTAGGGAGATGGT A C SRCAP Ensembl:ENSG00000080603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30699166..30699252 26863196 MeRIP-seq:(Medium) rs1376202576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261002,Human_RBP_ID_4364499,Human_RBP_ID_5087943,Human_RBP_ID_12719397,Human_RBP_ID_18677717,Human_RBP_ID_21971244,Human_RBP_ID_26769126 Human_Splice_Rec_1703663 85163 RMVar_ID_85163 Human_SNP_ID_599571606 m1A Human chr16 + 30699169 30699169 30699169 TGGCAACTTGGGCAGAGGTCAGGGGTCACGCGAGGTCAGTCCGTCGGGAGGGCTAGGGAGATGGT TGGCAACTTGGGCAGAGGTCAGGGGTCACGCGTGGTCAGTCCGTCGGGAGGGCTAGGGAGATGGT A T SRCAP Ensembl:ENSG00000080603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30699166..30699252 26863196 MeRIP-seq:(Medium) rs1376202576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261002,Human_RBP_ID_4364499,Human_RBP_ID_5087943,Human_RBP_ID_12719397,Human_RBP_ID_18677717,Human_RBP_ID_21971244,Human_RBP_ID_26769126 Human_Splice_Rec_1703663 85164 RMVar_ID_85164 Human_SNP_ID_599572062 m1A Human chr16 + 30700708 30700708 30700708 TGGAAGGCGGGTCCCGGTGGCCGGTGGCCCAGAATGAGGCCAGCTCCCAGCATGCCCTGCAGCCG TGGAAGGCGGGTCCCGGTGGCCGGTGGCCCAGGATGAGGCCAGCTCCCAGCATGCCCTGCAGCCG A G SRCAP Ensembl:ENSG00000080603 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30700660..30700771 26863196 MeRIP-seq:(Medium) rs1319217497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472927,Human_RBP_ID_1177799,Human_RBP_ID_4394636,Human_RBP_ID_5236602,Human_RBP_ID_8811868,Human_RBP_ID_22801090,Human_RBP_ID_24558863,Human_RBP_ID_27240806 Human_Splice_Rec_1703660,Human_Splice_Rec_1703666 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_177919,RMVar_hsa_circ_370724,RMVar_hsa_circ_269023,RMVar_hsa_circ_102603,RMVar_hsa_circ_177920,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922 85165 RMVar_ID_85165 Human_SNP_ID_599574247 m1A Human chr16 - 30707344 30707344 30707344 AGACCTACCTTCCGGGCCACACCCCGTTTCCAACGGCGCTCCTGAGCAAAGTCAGCAGAGAGCCA AGACCTACCTTCCGGGCCACACCCCGTTTCCAGCGGCGCTCCTGAGCAAAGTCAGCAGAGAGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30707293..30707391 26863196 MeRIP-seq:(Medium) rs768944874 Functional Loss SNV dbSNP153 33..33 33 - - - 85166 RMVar_ID_85166 Human_SNP_ID_599574355 m1A Human chr16 + 30707621 30707621 30707621 CCGGCACCACGAGGAGCAGCGGCAGAAAGAGGAACGGGCCCGGAGGGAGGAGCAGGCCAAGCTGC CCGGCACCACGAGGAGCAGCGGCAGAAAGAGGGACGGGCCCGGAGGGAGGAGCAGGCCAAGCTGC A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:30707552..30707676;chr16:30707541..30707748 26863196 MeRIP-seq:(Medium) rs1415823021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816148,Human_RBP_ID_889653,Human_RBP_ID_4399324,Human_RBP_ID_5141901,Human_RBP_ID_5524331,Human_RBP_ID_9372652,Human_RBP_ID_26328894,Human_RBP_ID_26943265 Human_Splice_Rec_1703672,Human_Splice_Rec_1703673,Human_Splice_Rec_1703730,Human_Splice_Rec_1703731,Human_Splice_Rec_1703824,Human_Splice_Rec_1703825 RMVar_hsa_circ_98594,RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_105422,RMVar_hsa_circ_114545,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_177932,RMVar_hsa_circ_57072,RMVar_hsa_circ_89405,RMVar_hsa_circ_177933,RMVar_hsa_circ_177930,RMVar_hsa_circ_177931,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_368130,RMVar_hsa_circ_69571,RMVar_hsa_circ_177938,RMVar_hsa_circ_177936,RMVar_hsa_circ_362027 85167 RMVar_ID_85167 Human_SNP_ID_599575074 m1A Human chr16 + 30710092 30710092 30710092 TCTCATGATAGTGACACCCGAGATGGGCCTGAAGAAGGTGCTGAAGAAGAGCCCCCTCAGGTGTT TCTCATGATAGTGACACCCGAGATGGGCCTGACGAAGGTGCTGAAGAAGAGCCCCCTCAGGTGTT A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30709688..30710778 32194978 MeRIP-seq:(Medium) rs749346607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004143,Human_RBP_ID_1516804,Human_RBP_ID_1841458,Human_RBP_ID_3949106,Human_RBP_ID_5524336,Human_RBP_ID_6508172,Human_RBP_ID_8252082,Human_RBP_ID_8811871,Human_RBP_ID_9372657,Human_RBP_ID_17883807,Human_RBP_ID_18677761,Human_RBP_ID_26328897 Human_Splice_Rec_1703677,Human_Splice_Rec_1703735,Human_Splice_Rec_1703785,Human_Splice_Rec_1703829 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_105422,RMVar_hsa_circ_114545,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_177932,RMVar_hsa_circ_57072,RMVar_hsa_circ_89405,RMVar_hsa_circ_177930,RMVar_hsa_circ_177931,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_36082,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_69571,RMVar_hsa_circ_177936,RMVar_hsa_circ_351892 85168 RMVar_ID_85168 Human_SNP_ID_599575075 m1A Human chr16 + 30710092 30710092 30710092 TCTCATGATAGTGACACCCGAGATGGGCCTGAAGAAGGTGCTGAAGAAGAGCCCCCTCAGGTGTT TCTCATGATAGTGACACCCGAGATGGGCCTGAGGAAGGTGCTGAAGAAGAGCCCCCTCAGGTGTT A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30709688..30710778 32194978 MeRIP-seq:(Medium) rs749346607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004143,Human_RBP_ID_1516804,Human_RBP_ID_1841458,Human_RBP_ID_3949106,Human_RBP_ID_5524336,Human_RBP_ID_6508172,Human_RBP_ID_8252082,Human_RBP_ID_8811871,Human_RBP_ID_9372657,Human_RBP_ID_17883807,Human_RBP_ID_18677761,Human_RBP_ID_26328897 Human_Splice_Rec_1703677,Human_Splice_Rec_1703735,Human_Splice_Rec_1703785,Human_Splice_Rec_1703829 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_105422,RMVar_hsa_circ_114545,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_177932,RMVar_hsa_circ_57072,RMVar_hsa_circ_89405,RMVar_hsa_circ_177930,RMVar_hsa_circ_177931,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_36082,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_69571,RMVar_hsa_circ_177936,RMVar_hsa_circ_351892 85169 RMVar_ID_85169 Human_SNP_ID_599575739 m1A Human chr16 + 30711962 30711962 30711962 GAGTCTGAGGATGCCCAATCACAGAGCCAAGCAGATGAAGAGGAGGAAGATGATGATTTTGGGGT GAGTCTGAGGATGCCCAATCACAGAGCCAAGCCGATGAAGAGGAGGAAGATGATGATTTTGGGGT A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30711830..30712013 26863196 MeRIP-seq:(Medium) rs377073679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199724,Human_RBP_ID_1004145,Human_RBP_ID_1841471,Human_RBP_ID_3947586,Human_RBP_ID_4364681,Human_RBP_ID_6508189,Human_RBP_ID_8807039,Human_RBP_ID_18677781,Human_RBP_ID_21973071,Human_RBP_ID_22938504,Human_RBP_ID_23686803,Human_RBP_ID_26328903 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_57072,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_69571,RMVar_hsa_circ_177936,RMVar_hsa_circ_351892,RMVar_hsa_circ_97114,RMVar_hsa_circ_80443,RMVar_hsa_circ_96560,RMVar_hsa_circ_177939,RMVar_hsa_circ_120667,RMVar_hsa_circ_177940,RMVar_hsa_circ_117833,RMVar_hsa_circ_177941,RMVar_hsa_circ_177942,RMVar_hsa_circ_177944 85170 RMVar_ID_85170 Human_SNP_ID_599575740 m1A Human chr16 + 30711962 30711962 30711962 GAGTCTGAGGATGCCCAATCACAGAGCCAAGCAGATGAAGAGGAGGAAGATGATGATTTTGGGGT GAGTCTGAGGATGCCCAATCACAGAGCCAAGCGGATGAAGAGGAGGAAGATGATGATTTTGGGGT A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30711830..30712013 26863196 MeRIP-seq:(Medium) rs377073679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199724,Human_RBP_ID_1004145,Human_RBP_ID_1841471,Human_RBP_ID_3947586,Human_RBP_ID_4364681,Human_RBP_ID_6508189,Human_RBP_ID_8807039,Human_RBP_ID_18677781,Human_RBP_ID_21973071,Human_RBP_ID_22938504,Human_RBP_ID_23686803,Human_RBP_ID_26328903 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_57072,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_69571,RMVar_hsa_circ_177936,RMVar_hsa_circ_351892,RMVar_hsa_circ_97114,RMVar_hsa_circ_80443,RMVar_hsa_circ_96560,RMVar_hsa_circ_177939,RMVar_hsa_circ_120667,RMVar_hsa_circ_177940,RMVar_hsa_circ_117833,RMVar_hsa_circ_177941,RMVar_hsa_circ_177942,RMVar_hsa_circ_177944 85171 RMVar_ID_85171 Human_SNP_ID_599578394 m1A Human chr16 + 30720296 30720296 30720296 CTGTTAGAAGTGGCTACTGCTCCTGACCCCCCACCCCGGCCCAAGCCAGTCAAGATGAAGGTCAA CTGTTAGAAGTGGCTACTGCTCCTGACCCCCCCCCCCGGCCCAAGCCAGTCAAGATGAAGGTCAA A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30720249..30720881 32194978 MeRIP-seq:(Medium) rs145842115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233183,Human_RBP_ID_895757,Human_RBP_ID_5465890,Human_RBP_ID_5524352,Human_RBP_ID_8807078,Human_RBP_ID_12720101,Human_RBP_ID_18983659,Human_RBP_ID_20114827,Human_RBP_ID_24370664,Human_RBP_ID_26328909 Human_Splice_Rec_1703699,Human_Splice_Rec_1703757,Human_Splice_Rec_1703807,Human_Splice_Rec_1703851 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_120311,RMVar_hsa_circ_117166,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_9612,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_112480,RMVar_hsa_circ_83042,RMVar_hsa_circ_115989,RMVar_hsa_circ_177949,RMVar_hsa_circ_177948,RMVar_hsa_circ_177953,RMVar_hsa_circ_80195,RMVar_hsa_circ_177954 85172 RMVar_ID_85172 Human_SNP_ID_599578618 m1A Human chr16 - 30720926 30720926 30720926 TTGGGCTGCAGTGGAGGCAAGAGGACAGGGCCAGGAGGCCGAGATGCAGGAATAAGCGGGGGCCC TTGGGCTGCAGTGGAGGCAAGAGGACAGGGCCGGGAGGCCGAGATGCAGGAATAAGCGGGGGCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30720876..30720950 26863196 MeRIP-seq:(Medium) rs140807165 Functional Loss SNV dbSNP153 33..33 33 - - - 85173 RMVar_ID_85173 Human_SNP_ID_599579380 m1A Human chr16 - 30723189 30723189 30723189 TCAGGTGAAGGACTGTGGACCAGCTTGAGAAGAGGCCTCACCAGAGTGGGTGTGGGCATGGGGGC TCAGGTGAAGGACTGTGGACCAGCTTGAGAAGGGGCCTCACCAGAGTGGGTGTGGGCATGGGGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr16:30723151..30723225;chr16:30723101..30723250 26863196 MeRIP-seq:(Medium) rs755835433 Functional Loss SNV dbSNP153 33..33 33 - - - 85174 RMVar_ID_85174 Human_SNP_ID_599579381 m1A Human chr16 - 30723189 30723189 30723189 TCAGGTGAAGGACTGTGGACCAGCTTGAGAAGAGGCCTCACCAGAGTGGGTGTGGGCATGGGGGC TCAGGTGAAGGACTGTGGACCAGCTTGAGAAGCGGCCTCACCAGAGTGGGTGTGGGCATGGGGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr16:30723151..30723225;chr16:30723101..30723250 26863196 MeRIP-seq:(Medium) rs755835433 Functional Loss SNV dbSNP153 33..33 33 - - - 85175 RMVar_ID_85175 Human_SNP_ID_599579587 m1A Human chr16 + 30723799 30723799 30723799 CTGCCCCAGCCTCGGCTCCACTCACCATCCCCATCTCAGCCCCCTTGACTGTTTCTGCTTCGGGC CTGCCCCAGCCTCGGCTCCACTCACCATCCCCCTCTCAGCCCCCTTGACTGTTTCTGCTTCGGGC A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30723626..30723912 26863196 MeRIP-seq:(Medium) rs1198863848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472955,Human_RBP_ID_1238045,Human_RBP_ID_3949117,Human_RBP_ID_5128118,Human_RBP_ID_17077478,Human_RBP_ID_17256661,Human_RBP_ID_17369542,Human_RBP_ID_17486155,Human_RBP_ID_18190021,Human_RBP_ID_18939032,Human_RBP_ID_20114929,Human_RBP_ID_22200683,Human_RBP_ID_22421751,Human_RBP_ID_22801164,Human_RBP_ID_26943372,Human_RBP_ID_27240860,Human_RBP_ID_27441690 Human_miRNA_ID_2026596 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171 85176 RMVar_ID_85176 Human_SNP_ID_599579610 m1A Human chr16 + 30723861 30723861 30723861 GGCCCAGCTCTGTTGACCAGTGTGACTCCACCATTGGCACCTGTTGTCCCAGCGGCTCCTGGACC GGCCCAGCTCTGTTGACCAGTGTGACTCCACCGTTGGCACCTGTTGTCCCAGCGGCTCCTGGACC A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30723519..30723945 26863196 MeRIP-seq:(Medium) rs1161911847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_472957,Human_RBP_ID_1516854,Human_RBP_ID_1841511,Human_RBP_ID_3947589,Human_RBP_ID_4399375,Human_RBP_ID_5128118,Human_RBP_ID_6508246,Human_RBP_ID_12720179,Human_RBP_ID_17077909,Human_RBP_ID_17254000,Human_RBP_ID_17369543,Human_RBP_ID_17486156,Human_RBP_ID_18940227,Human_RBP_ID_20114933,Human_RBP_ID_22054057,Human_RBP_ID_22200684,Human_RBP_ID_22801166,Human_RBP_ID_23686849,Human_RBP_ID_25206277,Human_RBP_ID_27240860 Human_miRNA_ID_2890915 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171 85177 RMVar_ID_85177 Human_SNP_ID_599579759 m1A Human chr16 - 30724191 30724191 30724191 GGAGCCAGAATTGCTGTCTGTGGAGCCGCCATAGGAGCCAGAGGGGTGGCTAGAGCCTGAGATGC GGAGCCAGAATTGCTGTCTGTGGAGCCGCCATGGGAGCCAGAGGGGTGGCTAGAGCCTGAGATGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30724151..30724250 26863196 MeRIP-seq:(Medium) rs1416806403 Functional Loss SNV dbSNP153 33..33 33 - - - 85178 RMVar_ID_85178 Human_SNP_ID_599579866 m1A Human chr16 + 30724402 30724402 30724402 CAGCTCCAACCCCTGTGTTGGCTCCATCATCAACTCAAACTATGCTACCAGCCCCGGTTCCGTCA CAGCTCCAACCCCTGTGTTGGCTCCATCATCAGCTCAAACTATGCTACCAGCCCCGGTTCCGTCA A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30724351..30724525 26863196 MeRIP-seq:(Medium) rs767680249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004158,Human_RBP_ID_9284780,Human_RBP_ID_17254011,Human_RBP_ID_17369553,Human_RBP_ID_17486164,Human_RBP_ID_20114957,Human_RBP_ID_22200694,Human_RBP_ID_22938558,Human_RBP_ID_26943379,Human_RBP_ID_27240870,Human_RBP_ID_27441711 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171 85179 RMVar_ID_85179 Human_SNP_ID_599579884 m1A Human chr16 + 30724444 30724444 30724444 TGCTACCAGCCCCGGTTCCGTCACCTCTCCCGAGCCCGGCTTCTACGCAGACACTGGCCCTAGCC TGCTACCAGCCCCGGTTCCGTCACCTCTCCCGCGCCCGGCTTCTACGCAGACACTGGCCCTAGCC A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30724351..30724650 26863196 MeRIP-seq:(Medium) rs770273248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17254013,Human_RBP_ID_17369555,Human_RBP_ID_17486166,Human_RBP_ID_18677849,Human_RBP_ID_20170222,Human_RBP_ID_26328912 Human_miRNA_ID_3011698 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171 85180 RMVar_ID_85180 Human_SNP_ID_599579890 m1A Human chr16 - 30724452 30724452 30724452 AAAGCTGGGGCTAGGGCCAGTGTCTGCGTAGAAGCCGGGCTCGGGAGAGGTGACGGAACCGGGGC AAAGCTGGGGCTAGGGCCAGTGTCTGCGTAGACGCCGGGCTCGGGAGAGGTGACGGAACCGGGGC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30724401..30724525 26863196 MeRIP-seq:(Medium) rs1294469072 Functional Loss SNV dbSNP153 33..33 33 - - - 85181 RMVar_ID_85181 Human_SNP_ID_599580013 m1A Human chr16 + 30724721 30724721 30724721 TCCAGCTTCTCCAGTGGGCCCAGCCCCAGCTCACACGCTGACTTTGGCTCCAGCATCGTCATCTG TCCAGCTTCTCCAGTGGGCCCAGCCCCAGCTCCCACGCTGACTTTGGCTCCAGCATCGTCATCTG A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30724672..30725056 26863196 MeRIP-seq:(Medium) rs1264427741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17254019,Human_RBP_ID_17369560,Human_RBP_ID_17486172,Human_RBP_ID_20170225,Human_RBP_ID_22200700,Human_RBP_ID_22801178,Human_RBP_ID_27240875,Human_RBP_ID_27441715 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171 85182 RMVar_ID_85182 Human_SNP_ID_599581430 m1A Human chr16 - 30729473 30729473 30729473 AGGACGAGCCCGGGGCCAGAGCTCAGAGGCCAATTGCTCCTGGAAGGCTGCCTGACGTGGGGCCA AGGACGAGCCCGGGGCCAGAGCTCAGAGGCCAGTTGCTCCTGGAAGGCTGCCTGACGTGGGGCCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:30729284..30729500 26863196 MeRIP-seq:(Medium) rs376501621 Functional Loss SNV dbSNP153 33..33 33 - - - 85183 RMVar_ID_85183 Human_SNP_ID_599581455 m1A Human chr16 + 30729561 30729561 30729561 GCGCACCCAGTTCCCTGACTTAAGACTCATCCAGTATGATTGCGGTGAGTTTGTTGGCCAGTGTA GCGCACCCAGTTCCCTGACTTAAGACTCATCCGGTATGATTGCGGTGAGTTTGTTGGCCAGTGTA A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30729511..30733369 32194978 MeRIP-seq:(Medium) rs1350590124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1841540,Human_RBP_ID_3494285,Human_RBP_ID_6508310,Human_RBP_ID_8807122,Human_RBP_ID_9284782,Human_RBP_ID_12720501,Human_RBP_ID_18437559,Human_RBP_ID_18677888,Human_RBP_ID_19074149 Human_Splice_Rec_1703715,Human_Splice_Rec_1703771,Human_Splice_Rec_1703863 Human_miRNA_ID_2094530,Human_miRNA_ID_2718596 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_115989,RMVar_hsa_circ_177954,RMVar_hsa_circ_42150,RMVar_hsa_circ_177955,RMVar_hsa_circ_113171,RMVar_hsa_circ_273386,RMVar_hsa_circ_314412,RMVar_hsa_circ_360349,RMVar_hsa_circ_302438,RMVar_hsa_circ_272815,RMVar_hsa_circ_177956,RMVar_hsa_circ_177957 85184 RMVar_ID_85184 Human_SNP_ID_599583515 m1A Human chr16 + 30736593 30736593 30736593 TGCCATGAAATTCCTGGAGGCCTCACTGGAGGAGGTGAGCCGAGAGGAGCTCAAACAGGCAGAAG TGCCATGAAATTCCTGGAGGCCTCACTGGAGGGGGTGAGCCGAGAGGAGCTCAAACAGGCAGAAG A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30736347..30736594 32194978 MeRIP-seq:(Medium) rs1028295006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816153,Human_RBP_ID_5465716,Human_RBP_ID_5524375,Human_RBP_ID_6508352,Human_RBP_ID_8083152,Human_RBP_ID_8807151,Human_RBP_ID_9286260,Human_RBP_ID_18677903,Human_RBP_ID_18986079,Human_RBP_ID_22200757,Human_RBP_ID_22944848 Human_Splice_Rec_1703726,Human_Splice_Rec_1703727,Human_Splice_Rec_1703782,Human_Splice_Rec_1703783,Human_Splice_Rec_1703874,Human_Splice_Rec_1703875 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_63796,RMVar_hsa_circ_42150,RMVar_hsa_circ_360349,RMVar_hsa_circ_105032,RMVar_hsa_circ_21056,RMVar_hsa_circ_177962 85185 RMVar_ID_85185 Human_SNP_ID_599584468 m1A Human chr16 + 30738911 30738911 30738911 GATTTGCCCATCCCTGGGACCATTTCCTCTGCAGGGGATGGCAACTCCGAAAGTCGGACACAGCC GATTTGCCCATCCCTGGGACCATTTCCTCTGCGGGGGATGGCAACTCCGAAAGTCGGACACAGCC A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30738864..30739067 26863196 MeRIP-seq:(Medium) rs1423505888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43874,Human_RBP_ID_4365020,Human_RBP_ID_12720736,Human_RBP_ID_17371736,Human_RBP_ID_18940239,Human_RBP_ID_22050002,Human_RBP_ID_22200791,Human_RBP_ID_26636953,Human_RBP_ID_26943473,Human_RBP_ID_27240932,Human_RBP_ID_27441821 Human_miRNA_ID_2273557 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_42150,RMVar_hsa_circ_105032,RMVar_hsa_circ_177962 85186 RMVar_ID_85186 Human_SNP_ID_599584483 m1A Human chr16 + 30738944 30738944 30738944 GGGGATGGCAACTCCGAAAGTCGGACACAGCCACCCCCACACCCATCACCCCTAACCCCACTCCC GGGGATGGCAACTCCGAAAGTCGGACACAGCCTCCCCCACACCCATCACCCCTAACCCCACTCCC A T AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30738896..30739093 26863196 MeRIP-seq:(Medium) rs745919757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5465018,Human_RBP_ID_17371736,Human_RBP_ID_22938627,Human_RBP_ID_27240932,Human_RBP_ID_27441822 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_42150,RMVar_hsa_circ_105032,RMVar_hsa_circ_177962 85187 RMVar_ID_85187 Human_SNP_ID_599584501 m1A Human chr16 - 30738973 30738973 30738973 CAGTAGCAGTGGGACAAACTAGCAGTGGTGGGAGTGGGGTTAGGGGTGATGGGTGTGGGGGTGGC CAGTAGCAGTGGGACAAACTAGCAGTGGTGGGTGTGGGGTTAGGGGTGATGGGTGTGGGGGTGGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30738925..30739045 26863196 MeRIP-seq:(Medium) rs764905020 Functional Loss SNV dbSNP153 33..33 33 - - - 85188 RMVar_ID_85188 Human_SNP_ID_599584505 m1A Human chr16 + 30738977 30738977 30738977 CCCCCACACCCATCACCCCTAACCCCACTCCCACCACTGCTAGTTTGTCCCACTGCTACTGTTGC CCCCCACACCCATCACCCCTAACCCCACTCCCGCCACTGCTAGTTTGTCCCACTGCTACTGTTGC A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:30738875..30739024 26863410 MeRIP-seq:(Medium) rs765814249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5465018,Human_RBP_ID_12720739,Human_RBP_ID_17078688,Human_RBP_ID_18677937,Human_RBP_ID_18940240,Human_RBP_ID_22497765,Human_RBP_ID_27441822 Human_miRNA_ID_1702634,Human_miRNA_ID_1702635 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_42150,RMVar_hsa_circ_105032,RMVar_hsa_circ_177962 85189 RMVar_ID_85189 Human_SNP_ID_599584814 m1A Human chr16 - 30739613 30739613 30739613 TGGTTGGTGGTCCCAACAAGCCGGCGGGGGCCAGGACGTCGGCGTGGGGTCCCATCCCCTTCCTC TGGTTGGTGGTCCCAACAAGCCGGCGGGGGCCGGGACGTCGGCGTGGGGTCCCATCCCCTTCCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30739562..30739812 32194978 MeRIP-seq:(Medium) rs1252538188 Functional Loss SNV dbSNP153 33..33 33 - - - 85190 RMVar_ID_85190 Human_SNP_ID_599588401 m1A Human chr16 + 30751323 30751323 30751323 TCTTCCTTGCTCCTGTTAGCAGACGACCCCCCACCTCCTGCTGGCCCTGCCCATAGCCCACTTCC TCTTCCTTGCTCCTGTTAGCAGACGACCCCCCGCCTCCTGCTGGCCCTGCCCATAGCCCACTTCC A G PHKG2,AC106886.2 Ensembl:ENSG00000156873,Ensembl:ENSG00000260899 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30751291..30751418 26863196 MeRIP-seq:(Medium) rs1320063952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_893051,Human_RBP_ID_3510095,Human_RBP_ID_5128627,Human_RBP_ID_5184187,Human_RBP_ID_8188857,Human_RBP_ID_17077482,Human_RBP_ID_18162964,Human_RBP_ID_19071408,Human_RBP_ID_24413737 Human_miRNA_ID_3162845,Human_miRNA_ID_3178439,Human_miRNA_ID_3183636,Human_miRNA_ID_3188793,Human_miRNA_ID_3189857,Human_miRNA_ID_3213557 RMVar_hsa_circ_94559,RMVar_hsa_circ_126266,RMVar_hsa_circ_177963,RMVar_hsa_circ_38687,RMVar_hsa_circ_177964,RMVar_hsa_circ_177965 85191 RMVar_ID_85191 Human_SNP_ID_599588414 m1A Human chr16 - 30751344 30751344 30751344 AGGTGTGGAGGCAATGTTGGCGGAAGTGGGCTATGGGCAGGGCCAGCAGGAGGTGGGGGGTCGTC AGGTGTGGAGGCAATGTTGGCGGAAGTGGGCTGTGGGCAGGGCCAGCAGGAGGTGGGGGGTCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30751293..30751544 26863196 MeRIP-seq:(Medium) rs771481793 Functional Loss SNV dbSNP153 33..33 33 - - - 85192 RMVar_ID_85192 Human_SNP_ID_599591402 m1A Human chr16 - 30760504 30760504 30760504 GAATGGCTGACTCCAAAGCATGTGGTGGGTGTAGGGTGATGAAAGGAGGCCCAGTTGTCACTCAC GAATGGCTGACTCCAAAGCATGTGGTGGGTGTGGGGTGATGAAAGGAGGCCCAGTTGTCACTCAC T C CCDC189 Ensembl:ENSG00000196118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30760465..30760593 26863196 MeRIP-seq:(Medium) rs918656175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890538,Human_RBP_ID_5360186,Human_RBP_ID_22541525,Human_RBP_ID_22651980 RMVar_hsa_circ_25560 85193 RMVar_ID_85193 Human_SNP_ID_599591661 m1A Human chr16 + 30761254 30761254 30761254 AGCGGCGGCTGCGGAAAGAAAGCGAATTGGGGAAGGCAGCTGCGGTGTCCTGGCCCGTAGCGAAT AGCGGCGGCTGCGGAAAGAAAGCGAATTGGGGCAGGCAGCTGCGGTGTCCTGGCCCGTAGCGAAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30761251..30761319 26863196 MeRIP-seq:(Medium) rs369677903 Functional Loss SNV dbSNP153 33..33 33 - - - 85194 RMVar_ID_85194 Human_SNP_ID_599591887 m1A Human chr16 + 30761656 30761656 30761656 GTCCGCGCGGCCGACCCATGCACTGAGCTGCGATCCTTCCCCGCTTCCCGCCGCAGCTCGGAGAG GTCCGCGCGGCCGACCCATGCACTGAGCTGCGCTCCTTCCCCGCTTCCCGCCGCAGCTCGGAGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30761543..30761847 26863196 MeRIP-seq:(Medium) rs1477885972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5495558 85195 RMVar_ID_85195 Human_SNP_ID_599592014 m1A Human chr16 - 30762033 30762033 30762033 CTCGTATTAGCAACCTGGAAGAGAGGGCGCCCAGGTGGGCACTCGCAACTTCTCACGTATCTGCG CTCGTATTAGCAACCTGGAAGAGAGGGCGCCCGGGTGGGCACTCGCAACTTCTCACGTATCTGCG T C CCDC189 Ensembl:ENSG00000196118 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30761493..30762064 26863196 MeRIP-seq:(Medium) rs899179841 Functional Loss SNV dbSNP153 33..33 33 - - - 85196 RMVar_ID_85196 Human_SNP_ID_599594681 m1A Human chr16 + 30769401 30769401 30769401 GGCGAGCAGGTCCTTGGCCTCAAGTCCCAGGTATGGCCGCCGCCAGCTTGCAGACTGGAGCTGGA GGCGAGCAGGTCCTTGGCCTCAAGTCCCAGGTGTGGCCGCCGCCAGCTTGCAGACTGGAGCTGGA A G RNF40 Ensembl:ENSG00000103549 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30769398..30769498 32194978 MeRIP-seq:(Medium) rs908633448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889673,Human_RBP_ID_19074192,Human_RBP_ID_22053185,Human_RBP_ID_26328927 RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970 85197 RMVar_ID_85197 Human_SNP_ID_599594729 m1A Human chr16 + 30769507 30769507 30769507 GTGGATGCCCAGCTGCTGACTGTGCAGAAGCTAGAGGAGAAGGAGCGAGCCTTGCAGGGCAGCCT GTGGATGCCCAGCTGCTGACTGTGCAGAAGCTGGAGGAGAAGGAGCGAGCCTTGCAGGGCAGCCT A G RNF40 Ensembl:ENSG00000103549 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30769381..30769523 26863196 MeRIP-seq:(Medium) rs4889506 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_761145,Human_RBP_ID_891990,Human_RBP_ID_5114226,Human_RBP_ID_8812362,Human_RBP_ID_18419472,Human_RBP_ID_19071419,Human_RBP_ID_26328139,Human_RBP_ID_27811797 Human_Splice_Rec_1704174,Human_Splice_Rec_1704175,Human_Splice_Rec_1704226,Human_Splice_Rec_1704227,Human_Splice_Rec_1704260,Human_Splice_Rec_1704261,Human_Splice_Rec_1704303,Human_Splice_Rec_1704320,Human_Splice_Rec_1704321 Clinvar_Rec_443,Clinvar_Rec_444 RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970,RMVar_hsa_circ_177973,RMVar_hsa_circ_344728 85198 RMVar_ID_85198 Human_SNP_ID_599595474 m1A Human chr16 + 30771926 30771926 30771926 GGCTGCGGGAGATCCAGCCCTGCCTGGCAGAGAGCCGGGCTGCTCGTGAGAAAGAGAGCTTCAAC GGCTGCGGGAGATCCAGCCCTGCCTGGCAGAGGGCCGGGCTGCTCGTGAGAAAGAGAGCTTCAAC A G RNF40 Ensembl:ENSG00000103549 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30769597..30771929 32194978 MeRIP-seq:(Medium) rs1184977818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1841646,Human_RBP_ID_5524385,Human_RBP_ID_18437584,Human_RBP_ID_26330024 Human_Splice_Rec_1704176,Human_Splice_Rec_1704177,Human_Splice_Rec_1704228,Human_Splice_Rec_1704229,Human_Splice_Rec_1704262,Human_Splice_Rec_1704263,Human_Splice_Rec_1704304,Human_Splice_Rec_1704305,Human_Splice_Rec_1704322,Human_Splice_Rec_1704323 RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970,RMVar_hsa_circ_325877 85199 RMVar_ID_85199 Human_SNP_ID_599596247 m1A Human chr16 - 30774677 30774677 30774677 AAGCAAGTGATGCCCCCATCTGCCAAGAGGGTACCTCCTTCAGCCCTTGGCACAAGAGCCAGACC AAGCAAGTGATGCCCCCATCTGCCAAGAGGGTGCCTCCTTCAGCCCTTGGCACAAGAGCCAGACC T C AC106886.5 Ensembl:ENSG00000280211 Other exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:30774626..30774800 32194978 MeRIP-seq:(Medium) rs1056988095 Functional Loss SNV dbSNP153 33..33 33 - - - 85200 RMVar_ID_85200 Human_SNP_ID_599599824 m1A Human chr16 + 30787071 30787057 30787071 CTGGGAAAAGCCGGAAGGCGGAATCCAGCCCCAGGGGACTTAACCCCTTCAGTGCCCTGCCTCGG CTGGGAAAAGCCGGAAGGC______________GGGGACTTAACCCCTTCAGTGCCCTGCCTCGG CGGAATCCAGCCCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30787068..30787156 26863196 MeRIP-seq:(Medium) rs1006066330 Functional Loss DEL dbSNP153 20..33 33 - - - 85201 RMVar_ID_85201 Human_SNP_ID_599599853 m1A Human chr16 + 30787155 30787155 30787155 GGACTCTGGGGTCCTTCTCAAGGGGTGATTCCAGGCTGAGGACCCGGGGACCAGTTCAGGGTGAC GGACTCTGGGGTCCTTCTCAAGGGGTGATTCCGGGCTGAGGACCCGGGGACCAGTTCAGGGTGAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30787050..30787165 26863196 MeRIP-seq:(Medium) rs959693048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6508668,Human_RBP_ID_12721832 85202 RMVar_ID_85202 Human_SNP_ID_599611836 m1A Human chr16 + 30834450 30834450 30834450 GTGCACGGGCCTCAACATATGCATGGACGTCCAGGTGCCACGTGGGCATCTCGTGGTGCTGCAGA GTGCACGGGCCTCAACATATGCATGGACGTCCCGGTGCCACGTGGGCATCTCGTGGTGCTGCAGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30834325..30834625 32194978 MeRIP-seq:(Medium) rs1261193462 Functional Loss SNV dbSNP153 33..33 33 - - - 85203 RMVar_ID_85203 Human_SNP_ID_599617849 m1A Human chr16 + 30860732 30860732 30860732 ACACATCAGTCCCTCCCTAGTCTCTGCTCCCAATGTGACTCGTCCCAAATCTTTCCTCTTTCTCT ACACATCAGTCCCTCCCTAGTCTCTGCTCCCAGTGTGACTCGTCCCAAATCTTTCCTCTTTCTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30860719..30860968 26863196 MeRIP-seq:(Medium) rs1029312028 Functional Loss SNV dbSNP153 33..33 33 - - - 85204 RMVar_ID_85204 Human_SNP_ID_599618071 m1A Human chr16 + 30861727 30861727 30861727 CAGTGGAGGGTAACTCCGTCCCCTTCTTAATCAATATGGAGGCTACCCACTCCACATTACCTTCT CAGTGGAGGGTAACTCCGTCCCCTTCTTAATCCATATGGAGGCTACCCACTCCACATTACCTTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30861725..30861818 26863196 MeRIP-seq:(Medium) rs1469120495 Functional Loss SNV dbSNP153 33..33 33 - - - 85205 RMVar_ID_85205 Human_SNP_ID_599618590 m1A Human chr16 - 30863638 30863637 30863638 GGGAGAGTAGGTGGGCGTGACCGATGAGAAGGAGAAAAACTAGCCGTGAGGGACAGAAGTTGGAA GGGAGAGTAGGTGGGCGTGACCGATGAGAAGG_GAAAAACTAGCCGTGAGGGACAGAAGTTGGAA CT C BCL7C Ensembl:ENSG00000099385 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30863632..30863791 26863196 MeRIP-seq:(Medium) rs747892984 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23687021 85206 RMVar_ID_85206 Human_SNP_ID_599618593 m1A Human chr16 - 30863647 30863647 30863647 AGTTTCAGTGGGAGAGTAGGTGGGCGTGACCGATGAGAAGGAGAAAAACTAGCCGTGAGGGACAG AGTTTCAGTGGGAGAGTAGGTGGGCGTGACCGGTGAGAAGGAGAAAAACTAGCCGTGAGGGACAG T C BCL7C Ensembl:ENSG00000099385 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30863642..30863732;chr16:30863638..30863742 26863196 MeRIP-seq:(Medium) rs927928084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23687021 85207 RMVar_ID_85207 Human_SNP_ID_599618660 m1A Human chr16 - 30864021 30864021 30864021 AGAGAGTCAGTGAGATTGATAGTGTGATGGAGATAGCTGGGGAGAGGTAGAGGGTGACGTAAGAA AGAGAGTCAGTGAGATTGATAGTGTGATGGAGGTAGCTGGGGAGAGGTAGAGGGTGACGTAAGAA T C BCL7C Ensembl:ENSG00000099385 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30863984..30864068 26863196 MeRIP-seq:(Medium) rs1049365497 Functional Loss SNV dbSNP153 33..33 33 - - - 85208 RMVar_ID_85208 Human_SNP_ID_599626238 m1A Human chr16 - 30893911 30893911 30893911 TGGCCGGCCGGACTGTACGGGCCGAGACCCGGAGCCGGGCCAAGGATGACATCAAGAAGGTGATG TGGCCGGCCGGACTGTACGGGCCGAGACCCGGCGCCGGGCCAAGGATGACATCAAGAAGGTGATG T G AC135048.2,BCL7C Ensembl:ENSG00000262721,Ensembl:ENSG00000099385 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30893876..30894050 26863196 MeRIP-seq:(Medium) rs867885079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473161,Human_RBP_ID_4393036,Human_RBP_ID_5180676,Human_RBP_ID_8941343,Human_RBP_ID_17653011 Human_Splice_Rec_1704333,Human_Splice_Rec_1704343,Human_Splice_Rec_1704353,Human_Splice_Rec_1704363 85209 RMVar_ID_85209 Human_SNP_ID_599626245 m1A Human chr16 - 30893927 30893927 30893927 CCCAGCCCCGCCAGCATGGCCGGCCGGACTGTACGGGCCGAGACCCGGAGCCGGGCCAAGGATGA CCCAGCCCCGCCAGCATGGCCGGCCGGACTGTGCGGGCCGAGACCCGGAGCCGGGCCAAGGATGA T C AC135048.2,BCL7C Ensembl:ENSG00000262721,Ensembl:ENSG00000099385 lincRNA,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30893876..30894050 26863196 MeRIP-seq:(Medium) rs1312966935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393036,Human_RBP_ID_8941343,Human_RBP_ID_17653011 Human_Splice_Rec_1704333,Human_Splice_Rec_1704343,Human_Splice_Rec_1704353,Human_Splice_Rec_1704363 85210 RMVar_ID_85210 Human_SNP_ID_599626290 m1A Human chr16 + 30894018 30894018 30894018 GCCTCCCGTCCGGCGGGCTCAGGCTCCGCGCCAGGCCCGGGCGCCGCGCTCTCGGCCTGCCGTCC GCCTCCCGTCCGGCGGGCTCAGGCTCCGCGCCGGGCCCGGGCGCCGCGCTCTCGGCCTGCCGTCC A G MIR762HG Ensembl:ENSG00000260083 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30892744..30894111;chr16:30887801..30894583;chr16:30887801..30894161 26863196 MeRIP-seq:(Medium) rs1383548311 Functional Loss SNV dbSNP153 33..33 33 - - - 85211 RMVar_ID_85211 Human_SNP_ID_599632000 m1A Human chr16 - 30917269 30917269 30917269 AACTGGGTATGGTGGTGCCCACGTGTAGTACCAGCTACTCGGGAGGCTGGGGTAGGAGATTGAGC AACTGGGTATGGTGGTGCCCACGTGTAGTACCGGCTACTCGGGAGGCTGGGGTAGGAGATTGAGC T C FBXL19-AS1,FBXL19-AS1:2 RNACentral:URS0000D5770D,RNACentral:URS0000D5C8FD lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30917228..30917391 26863196 MeRIP-seq:(Medium) rs1326830094 Functional Loss SNV dbSNP153 33..33 33 - - - 85212 RMVar_ID_85212 Human_SNP_ID_599632481 m1A Human chr16 - 30918818 30918815 30918818 AGGAGAAGAAGAAGAAAGAAGAAGGAAGGAAGAAAGAAGAAGGAAGGAGAAGAGGAAGAAAGAAG AGGAGAAGAAGAAGAAAGAAGAAGGAAGGAAG___GAAGAAGGAAGGAGAAGAGGAAGAAAGAAG CTTT C FBXL19-AS1,FBXL19-AS1:2 RNACentral:URS0000D5770D,RNACentral:URS0000D5C8FD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30918611..30919100 26863196 MeRIP-seq:(Medium) rs1446958309 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_25206752 85213 RMVar_ID_85213 Human_SNP_ID_599632481 m1A Human chr16 - 30918817 30918815 30918818 GGAGAAGAAGAAGAAAGAAGAAGGAAGGAAGAAAGAAGAAGGAAGGAGAAGAGGAAGAAAGAAGA GGAGAAGAAGAAGAAAGAAGAAGGAAGGAAG___GAAGAAGGAAGGAGAAGAGGAAGAAAGAAGA CTTT C FBXL19-AS1,FBXL19-AS1:2 RNACentral:URS0000D5770D,RNACentral:URS0000D5C8FD lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30918425..30919084;chr16:30918572..30919090 26863196 MeRIP-seq:(Medium) rs1446958309 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_25206752 85214 RMVar_ID_85214 Human_SNP_ID_599632483 m1A Human chr16 - 30918818 30918818 30918818 AGGAGAAGAAGAAGAAAGAAGAAGGAAGGAAGAAAGAAGAAGGAAGGAGAAGAGGAAGAAAGAAG AGGAGAAGAAGAAGAAAGAAGAAGGAAGGAAGGAAGAAGAAGGAAGGAGAAGAGGAAGAAAGAAG T C FBXL19-AS1,FBXL19-AS1:2 RNACentral:URS0000D5770D,RNACentral:URS0000D5C8FD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30918611..30919100 26863196 MeRIP-seq:(Medium) rs770497602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25206752 85215 RMVar_ID_85215 Human_SNP_ID_599634305 m1A Human chr16 + 30924244 30924244 30924244 AGCAGGACCTCCCCCTGGAAGGGCCGCGCCGCAGCCCGTGGGAGGGCCTCGCCCCCGGCGCCCCC AGCAGGACCTCCCCCTGGAAGGGCCGCGCCGCCGCCCGTGGGAGGGCCTCGCCCCCGGCGCCCCC A C FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr16:30924193..30924432;chr16:30924146..30924390 26863196 MeRIP-seq:(Medium) rs1407162505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3507148,Human_RBP_ID_9325092 85216 RMVar_ID_85216 Human_SNP_ID_599634351 m1A Human chr16 - 30924399 30924390 30924400 CCTTCTCGGCAGCTCCCGGCGGGTCGGCGGCCATCGGCGGCGGGGGGGCCGGGCGGCGCGGGGCG CCTTCTCGGCAGCTCCCGGCGGGTCGGCGGC__________GGGGGGGCCGGGCGGCGCGGGGCG CGCCGCCGATG C FBXL19-AS1 RNACentral:URS00009B83FC lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:30924076..30924475 26863410 MeRIP-seq:(Medium) rs934319365 Functional Loss DEL dbSNP153 32..41 33 - - - 85217 RMVar_ID_85217 Human_SNP_ID_599634708 m1A Human chr16 + 30925670 30925669 30925671 GCTCTAGCTGCCTGTAGGTGGAGGGACCTGTCAGGGGTCTCCCAGGCCAGGGCCCCAGTGGGCCC GCTCTAGCTGCCTGTAGGTGGAGGGACCTGTC__GGGTCTCCCAGGCCAGGGCCCCAGTGGGCCC CAG C FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30925669..30927319 26863410 MeRIP-seq:(Medium) rs1468508601 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22542362 85218 RMVar_ID_85218 Human_SNP_ID_599635329 m1A Human chr16 + 30927782 30927782 30927782 AGGTGAGGGGCCTGGCCGCCGTAGGGCCGACAACGGCGAGGAGGGCGCCAGCTTGGGGAGCGGAT AGGTGAGGGGCCTGGCCGCCGTAGGGCCGACAGCGGCGAGGAGGGCGCCAGCTTGGGGAGCGGAT A G FBXL19 Ensembl:ENSG00000099364 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30927647..30927870 26863196 MeRIP-seq:(Medium) rs1435960218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5763,Human_RBP_ID_5142797,Human_RBP_ID_18986135 Human_Splice_Rec_1704416,Human_Splice_Rec_1704436,Human_Splice_Rec_1704456,Human_Splice_Rec_1704476,Human_Splice_Rec_1704510 RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 85219 RMVar_ID_85219 Human_SNP_ID_599635347 m1A Human chr16 - 30927840 30927831 30927840 AGGGGGCCCTTGCGCCTGGGCGGGGGCGGTGGAAGCGGTGGCTCCTCTGTCAGCTTCCATCCGCT AGGGGGCCCTTGCGCCTGGGCGGGGGCGGTGG_________CTCCTCTGTCAGCTTCCATCCGCT GCCACCGCTT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30927675..30927899 26863196 MeRIP-seq:(Medium) rs200068009 Functional Loss DEL dbSNP153,HGVD 33..41 33 - - - 85220 RMVar_ID_85220 Human_SNP_ID_599636148 m1A Human chr16 + 30930213 30930212 30930214 GTGCCTGACACCTCCTCTTCCTCCTCGGACTCAGACTCCGACTCCGACTCTTCGGGCACATCGCT GTGCCTGACACCTCCTCTTCCTCCTCGGACTC__ACTCCGACTCCGACTCTTCGGGCACATCGCT CAG C FBXL19 Ensembl:ENSG00000099364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30930162..30930327 26863196 MeRIP-seq:(Medium) rs1491348766 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_473179,Human_RBP_ID_8807311,Human_RBP_ID_9374237,Human_RBP_ID_27447969 RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 85221 RMVar_ID_85221 Human_SNP_ID_599636149 m1A Human chr16 + 30930213 30930213 30930213 GTGCCTGACACCTCCTCTTCCTCCTCGGACTCAGACTCCGACTCCGACTCTTCGGGCACATCGCT GTGCCTGACACCTCCTCTTCCTCCTCGGACTCGGACTCCGACTCCGACTCTTCGGGCACATCGCT A G FBXL19 Ensembl:ENSG00000099364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30930162..30930327 26863196 MeRIP-seq:(Medium) rs779042030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473179,Human_RBP_ID_8807311,Human_RBP_ID_9374237,Human_RBP_ID_27447969 RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 85222 RMVar_ID_85222 Human_SNP_ID_599636185 m1A Human chr16 + 30930285 30930285 30930285 GACGAAGCCCCCGGCGAGGCCCGGAATGGGCGACGGCCAGCCCGGGGCAGCTCTGGCGAGAAGGA GACGAAGCCCCCGGCGAGGCCCGGAATGGGCGTCGGCCAGCCCGGGGCAGCTCTGGCGAGAAGGA A T FBXL19 Ensembl:ENSG00000099364 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30930051..30930575 26863196 MeRIP-seq:(Medium) rs757484824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_894213,Human_RBP_ID_9374237 Human_miRNA_ID_632374,Human_miRNA_ID_2151953,Human_miRNA_ID_2242025 RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 85223 RMVar_ID_85223 Human_SNP_ID_599637538 m1A Human chr16 - 30935409 30935407 30935410 TCTTAAGGGATCACTTCCCTTTCAGTTCCAAGAAAAGATGGAAGCCACCAGACAGGAAAGCCTGC TCTTAAGGGATCACTTCCCTTTCAGTTCCAA___AAGATGGAAGCCACCAGACAGGAAAGCCTGC TTTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30935405..30935631 26863196 MeRIP-seq:(Medium) rs548472628 Functional Loss DEL dbSNP153 32..34 33 - - - 85224 RMVar_ID_85224 Human_SNP_ID_599640406 m1A Human chr16 - 30946824 30946824 30946824 CTCAGGTCCAGGGCGCTCAGCTGGGGTGCGTGACGCAGCAGGAGACGCAGGGAGGCATCTGTCAG CTCAGGTCCAGGGCGCTCAGCTGGGGTGCGTGTCGCAGCAGGAGACGCAGGGAGGCATCTGTCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30946773..30947174 26863196 MeRIP-seq:(Medium) rs765683789 Functional Loss SNV dbSNP153 33..33 33 - - - 85225 RMVar_ID_85225 Human_SNP_ID_599640529 m1A Human chr16 - 30947182 30947182 30947182 AGCAGCTTCTCCTCAGGGCAGCGGAAGGGGCCAGGGGGCCCGGCAGCTGCCAGCCGGGCACAAGC AGCAGCTTCTCCTCAGGGCAGCGGAAGGGGCCGGGGGGCCCGGCAGCTGCCAGCCGGGCACAAGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30946826..30947370 26863410 MeRIP-seq:(Medium) rs1257541277 Functional Loss SNV dbSNP153 33..33 33 - - - 85226 RMVar_ID_85226 Human_SNP_ID_599640696 m1A Human chr16 - 30947777 30947777 30947777 GTATTGCTGTCCCCACACCTGCTCTCATCCCCACCTCCAGCTCAGCCCCAGCTTGCCCCTGGTTC GTATTGCTGTCCCCACACCTGCTCTCATCCCCCCCTCCAGCTCAGCCCCAGCTTGCCCCTGGTTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30947727..30947980 26863196 MeRIP-seq:(Medium) rs946302463 Functional Loss SNV dbSNP153 33..33 33 - - - 85227 RMVar_ID_85227 Human_SNP_ID_599640861 m1A Human chr16 - 30948243 30948243 30948243 TGACGATGAAAGAGTGGGAAGAGCCAGGCTGGAGGAGTCCCATGGTCCCCATTCTTGGGCTGGCG TGACGATGAAAGAGTGGGAAGAGCCAGGCTGGTGGAGTCCCATGGTCCCCATTCTTGGGCTGGCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30948119..30948283 26863196 MeRIP-seq:(Medium) rs1033213497 Functional Loss SNV dbSNP153 33..33 33 - - - 85228 RMVar_ID_85228 Human_SNP_ID_599641191 m1A Human chr16 - 30949186 30949186 30949186 CAAGCCCGGGGGCGGCCCCATTCCCAGACAGGACGAGCAGGATGCAGGCGGCGGGCGCCCAGGAA CAAGCCCGGGGGCGGCCCCATTCCCAGACAGGGCGAGCAGGATGCAGGCGGCGGGCGCCCAGGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30949135..30949214 26863196 MeRIP-seq:(Medium) rs4889582 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10151,GWAS_ID_10152 85229 RMVar_ID_85229 Human_SNP_ID_599643648 m1A Human chr16 - 30957845 30957829 30957845 TTCGCCTCGGCCGGCGCCCTGGGAGGCTCGGAAGTTGCGGCCCAGGGAGCTTGGAGATTGGCCGC TTCGCCTCGGCCGGCGCCCTGGGAGGCTCGGA________________GCTTGGAGATTGGCCGC CTCCCTGGGCCGCAACT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30957794..30957897 26863196 MeRIP-seq:(Medium) rs1181810579 Functional Loss DEL dbSNP153 33..48 33 - - - 85230 RMVar_ID_85230 Human_SNP_ID_599643764 m1A Human chr16 + 30958090 30958090 30958090 GCCGCCGCCTCGCGCCGCTGAGGTGCCGCGCGAGGTGGGGGGAGGGGGAGCCGCTCGCCGGGAGC GCCGCCGCCTCGCGCCGCTGAGGTGCCGCGCGTGGTGGGGGGAGGGGGAGCCGCTCGCCGGGAGC A T SETD1A Ensembl:ENSG00000099381 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:30958007..30958096 26863410 MeRIP-seq:(Medium) rs1384126373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394656,Human_RBP_ID_5358023,Human_RBP_ID_18419002,Human_RBP_ID_26779471 RMVar_hsa_circ_127545,RMVar_hsa_circ_177984 85231 RMVar_ID_85231 Human_SNP_ID_599645939 m1A Human chr16 - 30964313 30964313 30964313 CCAGGCGGGGTCTGCTCTGTACCTGCTGGAGTAGGCAGAGTCCTGAGAGTAGGGGGTGCTGCCCC CCAGGCGGGGTCTGCTCTGTACCTGCTGGAGTGGGCAGAGTCCTGAGAGTAGGGGGTGCTGCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30964163..30964336 26863196 MeRIP-seq:(Medium) rs1398021779 Functional Loss SNV dbSNP153 33..33 33 - - - 85232 RMVar_ID_85232 Human_SNP_ID_599646145 m1A Human chr16 - 30964760 30964760 30964760 TGACGAGGAGGACGAGGACAATGAGGAGGAAGAGGCGGAGGATGAGGCAGTGGCTGCAGTGGTGG TGACGAGGAGGACGAGGACAATGAGGAGGAAGTGGCGGAGGATGAGGCAGTGGCTGCAGTGGTGG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:30964710..30964850 26863196 MeRIP-seq:(Medium) rs762628420 Functional Loss SNV dbSNP153 33..33 33 - - - 85233 RMVar_ID_85233 Human_SNP_ID_599646335 m1A Human chr16 - 30965116 30965116 30965116 CCAGAGCGGGCAGGGGAGGCTGGGCGGGGGGAAGTCCGAACTTCTTCTCTCTCAGGGCTGGGCCC CCAGAGCGGGCAGGGGAGGCTGGGCGGGGGGATGTCCGAACTTCTTCTCTCTCAGGGCTGGGCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30964894..30965175 26863196 MeRIP-seq:(Medium) rs774823415 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 85234 RMVar_ID_85234 Human_SNP_ID_599650783 m1A Human chr16 - 30979236 30979236 30979236 GGTGGGGGCAGGAGGGGGATGGGAGAAGAGGGACGCTCATCGGGGCGTGGGGCAGGGGCCGGGGG GGTGGGGGCAGGAGGGGGATGGGAGAAGAGGGGCGCTCATCGGGGCGTGGGGCAGGGGCCGGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr16:30979130..30979336;chr16:30979137..30979307 26863196 MeRIP-seq:(Medium) rs1411988373 Functional Loss SNV dbSNP153 33..33 33 - - - 85235 RMVar_ID_85235 Human_SNP_ID_599651017 m1A Human chr16 - 30979653 30979653 30979653 TGCTCCAGGAGGATGTGGCTGAGCAGGGGCCTAGGGCGCTCGGCCTCGTCCGATGTCTCTGTGGC TGCTCCAGGAGGATGTGGCTGAGCAGGGGCCTGGGGCGCTCGGCCTCGTCCGATGTCTCTGTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30979536..30979964 26863196 MeRIP-seq:(Medium) rs1372502226 Functional Loss SNV dbSNP153 33..33 33 - - - 85236 RMVar_ID_85236 Human_SNP_ID_599651128 m1A Human chr16 + 30979865 30979864 30979865 CAAGCCGCAGCAACTGCAGCAGCAGCGGGAGGAGGGCGAAGAGGAGGGGGAGGAAGAGGGGGAGG CAAGCCGCAGCAACTGCAGCAGCAGCGGGAGG_GGGCGAAGAGGAGGGGGAGGAAGAGGGGGAGG GA G SETD1A Ensembl:ENSG00000099381 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30979741..30979900 26863196 MeRIP-seq:(Medium) rs372816613 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_43974 RMVar_hsa_circ_85722,RMVar_hsa_circ_177987 85237 RMVar_ID_85237 Human_SNP_ID_599651429 m1A Human chr16 - 30980462 30980462 30980462 AGGTTGGTGAGTGCAGGGTGTTAAGGAAGAGAACGGCTCCTCTCTGGCCACCTGCGTCCCAGCCA AGGTTGGTGAGTGCAGGGTGTTAAGGAAGAGAGCGGCTCCTCTCTGGCCACCTGCGTCCCAGCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30980456..30980578 26863196 MeRIP-seq:(Medium) rs1226410136 Functional Loss SNV dbSNP153 33..33 33 - - - 85238 RMVar_ID_85238 Human_SNP_ID_599651450 m1A Human chr16 + 30980505 30980505 30980505 AACACCCTGCACTCACCAACCTGACCACCCCAAAACGCAAGCGGCGGCCCCAGGATGGGCCCCGG AACACCCTGCACTCACCAACCTGACCACCCCAGAACGCAAGCGGCGGCCCCAGGATGGGCCCCGG A G SETD1A Ensembl:ENSG00000099381 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30980481..30980647 26863196 MeRIP-seq:(Medium) rs1234989678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43977,Human_RBP_ID_18469749 RMVar_hsa_circ_85722,RMVar_hsa_circ_177987 85239 RMVar_ID_85239 Human_SNP_ID_599651451 m1A Human chr16 + 30980505 30980505 30980505 AACACCCTGCACTCACCAACCTGACCACCCCAAAACGCAAGCGGCGGCCCCAGGATGGGCCCCGG AACACCCTGCACTCACCAACCTGACCACCCCACAACGCAAGCGGCGGCCCCAGGATGGGCCCCGG A C SETD1A Ensembl:ENSG00000099381 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30980481..30980647 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_43977,Human_RBP_ID_18469749 RMVar_hsa_circ_85722,RMVar_hsa_circ_177987 85240 RMVar_ID_85240 Human_SNP_ID_599652891 m1A Human chr16 - 30985272 30985272 30985272 TGCCTACCTGCAGCCGCTATCCCAGGGTGCCCAGACTGGCCTGGAGGGGCCCTCTTCTTTCGTCC TGCCTACCTGCAGCCGCTATCCCAGGGTGCCCCGACTGGCCTGGAGGGGCCCTCTTCTTTCGTCC T G AC135048.4 Ensembl:ENSG00000279196 Other exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30985225..30985365 26863196 MeRIP-seq:(Medium) rs1326336540 Functional Loss SNV dbSNP153 33..33 33 - - - 85241 RMVar_ID_85241 Human_SNP_ID_599653033 m1A Human chr16 - 30985613 30985613 30985613 AGAGACCTTGGCTCATCCAGGGGCTGGCTGCCACCTGCTGCAACCACCTGTTACTGCTGGAGGTG AGAGACCTTGGCTCATCCAGGGGCTGGCTGCCGCCTGCTGCAACCACCTGTTACTGCTGGAGGTG T C AC135048.4 Ensembl:ENSG00000279196 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30985608..30985781 26863196 MeRIP-seq:(Medium) rs540673827 Functional Loss SNV dbSNP153 33..33 33 - - - 85242 RMVar_ID_85242 Human_SNP_ID_599653122 m1A Human chr16 + 30985771 30985771 30985771 AATGCTGCTGCAGCGGGAGCCCCGGCTCGGGGAGCTGCGGGTCTTTGACCAACACCTGGGTCCCT AATGCTGCTGCAGCGGGAGCCCCGGCTCGGGGTGCTGCGGGTCTTTGACCAACACCTGGGTCCCT A T HSD3B7 Ensembl:ENSG00000099377 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30985676..30985777 32194978 MeRIP-seq:(Medium) rs1178555016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393048,Human_RBP_ID_18986155 Human_Splice_Rec_1704591,Human_Splice_Rec_1704601,Human_Splice_Rec_1704621 RMVar_hsa_circ_126485,RMVar_hsa_circ_177992 85243 RMVar_ID_85243 Human_SNP_ID_599656650 m1A Human chr16 + 30997140 30997140 30997140 CAGGGAGGGAGTCAGGGAGCAGAGACCGAGGCAGGTGAGGAGGCAGTGCATGGGCGGAATAAGGA CAGGGAGGGAGTCAGGGAGCAGAGACCGAGGCCGGTGAGGAGGCAGTGCATGGGCGGAATAAGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30997137..30997257 26863196 MeRIP-seq:(Medium) rs1184182060 Functional Loss SNV dbSNP153 33..33 33 - - - 85244 RMVar_ID_85244 Human_SNP_ID_599666284 m1A Human chr16 + 31035031 31035031 31035031 GAGAACTATAACTCCGTCAACACAAGAATGAGAAAAACCCAGGTGGGTTTTTTTTCTCAGAAATG GAGAACTATAACTCCGTCAACACAAGAATGAGGAAAACCCAGGTGGGTTTTTTTTCTCAGAAATG A G STX4 Ensembl:ENSG00000103496 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31034863..31038175 26863196 MeRIP-seq:(Medium) rs751049136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3494400,Human_RBP_ID_18983704 Human_Splice_Rec_1704674,Human_Splice_Rec_1704682,Human_Splice_Rec_1704683,Human_Splice_Rec_1704706,Human_Splice_Rec_1704707,Human_Splice_Rec_1704724,Human_Splice_Rec_1704725,Human_Splice_Rec_1704742,Human_Splice_Rec_1704743,Human_Splice_Rec_1704754,Human_Splice_Rec_1704755,Human_Splice_Rec_1704766,Human_Splice_Rec_1704767,Human_Splice_Rec_1704784,Human_Splice_Rec_1704785 RMVar_hsa_circ_367300,RMVar_hsa_circ_353508 85245 RMVar_ID_85245 Human_SNP_ID_599666285 m1A Human chr16 + 31035031 31035031 31035031 GAGAACTATAACTCCGTCAACACAAGAATGAGAAAAACCCAGGTGGGTTTTTTTTCTCAGAAATG GAGAACTATAACTCCGTCAACACAAGAATGAGTAAAACCCAGGTGGGTTTTTTTTCTCAGAAATG A T STX4 Ensembl:ENSG00000103496 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31034863..31038175 26863196 MeRIP-seq:(Medium) rs751049136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3494400,Human_RBP_ID_18983704 Human_Splice_Rec_1704674,Human_Splice_Rec_1704682,Human_Splice_Rec_1704683,Human_Splice_Rec_1704706,Human_Splice_Rec_1704707,Human_Splice_Rec_1704724,Human_Splice_Rec_1704725,Human_Splice_Rec_1704742,Human_Splice_Rec_1704743,Human_Splice_Rec_1704754,Human_Splice_Rec_1704755,Human_Splice_Rec_1704766,Human_Splice_Rec_1704767,Human_Splice_Rec_1704784,Human_Splice_Rec_1704785 RMVar_hsa_circ_367300,RMVar_hsa_circ_353508 85246 RMVar_ID_85246 Human_SNP_ID_599673025 m1A Human chr16 - 31061289 31061289 31061289 GCTCACACCCGGAGCTCCGGCCCTTCCCCTGCACCCAGTGCGGCAAGAGCTTCTCTGACCGGGCT GCTCACACCCGGAGCTCCGGCCCTTCCCCTGCGCCCAGTGCGGCAAGAGCTTCTCTGACCGGGCT T C ZNF668 Ensembl:ENSG00000167394 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31061240..31061556 32194978 MeRIP-seq:(Medium) rs1331709721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111739,RMVar_hsa_circ_178001,RMVar_hsa_circ_99732,RMVar_hsa_circ_178002 85247 RMVar_ID_85247 Human_SNP_ID_599673102 m1A Human chr16 + 31061446 31061446 31061446 CCCGCCTCGCCTGCCCCTTCCAAGGGACCAGGAGCCTCCCGGACACCAGCATCTTGGCATTCCAC CCCGCCTCGCCTGCCCCTTCCAAGGGACCAGGGGCCTCCCGGACACCAGCATCTTGGCATTCCAC A G AC135050.1 Ensembl:ENSG00000232748 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:31061397..31061593 26863196 MeRIP-seq:(Medium) rs776628449 Functional Loss SNV dbSNP153 33..33 33 - - - 85248 RMVar_ID_85248 Human_SNP_ID_599674185 m1A Human chr16 - 31064221 31064221 31064221 CAGTGGGGAGAAGGTGTCAGGCTCCGCGGCCAAGCCTAGGCCCTATGCGTGTCCGCTATGCCCCA CAGTGGGGAGAAGGTGTCAGGCTCCGCGGCCAGGCCTAGGCCCTATGCGTGTCCGCTATGCCCCA T C ZNF668 Ensembl:ENSG00000167394 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31064178..31064249 26863196 MeRIP-seq:(Medium) rs1228113391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2008937 RMVar_hsa_circ_99732,RMVar_hsa_circ_178002 85249 RMVar_ID_85249 Human_SNP_ID_599676878 m1A Human chr16 - 31073632 31073632 31073632 CATCAGGTAGGAAACGTCGGCGGGAAGCCGCGAGGGCCCCGGGCAGCTCCCACGCGGCCACGATC CATCAGGTAGGAAACGTCGGCGGGAAGCCGCGGGGGCCCCGGGCAGCTCCCACGCGGCCACGATC T C ZNF668 Ensembl:ENSG00000167394 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31073623..31073813 26863196 MeRIP-seq:(Medium) rs1239981248 Functional Loss SNV dbSNP153 33..33 33 - - - 85250 RMVar_ID_85250 Human_SNP_ID_599677260 m1A Human chr16 - 31074722 31074722 31074722 ATCTCGTCTGCCAATTTCCTCTCAGGACGCCTACCTCGCACCGGCGGCCCCCTCTCCTTCCCGCC ATCTCGTCTGCCAATTTCCTCTCAGGACGCCTGCCTCGCACCGGCGGCCCCCTCTCCTTCCCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31074719..31074971 26863196 MeRIP-seq:(Medium) rs969799113 Functional Loss SNV dbSNP153 33..33 33 - - - 85251 RMVar_ID_85251 Human_SNP_ID_599678574 m1A Human chr16 - 31078541 31078541 31078541 CCCTGGAAATGGGTCTCATCCCTCTCAAGCCCACATTTGTCCCCTTCAGATTCAGCCTGCAAACA CCCTGGAAATGGGTCTCATCCCTCTCAAGCCCGCATTTGTCCCCTTCAGATTCAGCCTGCAAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31078492..31078657 26863196 MeRIP-seq:(Medium) rs1009935207 Functional Loss SNV dbSNP153 33..33 33 - - - 85252 RMVar_ID_85252 Human_SNP_ID_599679261 m1A Human chr16 + 31080196 31080196 31080196 CATGGAACGGCGTGGGGGTGGGGGCACCCGAAAGGCGACTCGGGAAGATCGGCCCTTCCGCTGTG CATGGAACGGCGTGGGGGTGGGGGCACCCGAACGGCGACTCGGGAAGATCGGCCCTTCCGCTGTG A C ZNF646 Ensembl:ENSG00000167395 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31080149..31080254 32194978 MeRIP-seq:(Medium) rs946919593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22712225 85253 RMVar_ID_85253 Human_SNP_ID_599679262 m1A Human chr16 + 31080196 31080196 31080196 CATGGAACGGCGTGGGGGTGGGGGCACCCGAAAGGCGACTCGGGAAGATCGGCCCTTCCGCTGTG CATGGAACGGCGTGGGGGTGGGGGCACCCGAAGGGCGACTCGGGAAGATCGGCCCTTCCGCTGTG A G ZNF646 Ensembl:ENSG00000167395 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31080149..31080254 32194978 MeRIP-seq:(Medium) rs946919593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22712225 85254 RMVar_ID_85254 Human_SNP_ID_599679484 m1A Human chr16 + 31080654 31080654 31080654 TCCCAAGGCCAGGGGAGCGCAGTCAGAGCCCCATCAGGGCAGCAAGCTCAGAAGCCCCAGAGCCA TCCCAAGGCCAGGGGAGCGCAGTCAGAGCCCCGTCAGGGCAGCAAGCTCAGAAGCCCCAGAGCCA A G ZNF646 Ensembl:ENSG00000167395 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31080605..31080732 26863196 MeRIP-seq:(Medium) rs1480821022 Functional Loss SNV dbSNP153 33..33 33 - - - 85255 RMVar_ID_85255 Human_SNP_ID_599679950 m1A Human chr16 + 31081758 31081758 31081758 AGGAGGTGGGCACACAGTGGAGGGGGAAGTCCAGCCCCAAAGTCGGTGGGGGAGCAAGGAGTGAG AGGAGGTGGGCACACAGTGGAGGGGGAAGTCCCGCCCCAAAGTCGGTGGGGGAGCAAGGAGTGAG A C ZNF646 Ensembl:ENSG00000167395 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:31081708..31081922;chr16:31081707..31081916 26863196 MeRIP-seq:(Medium) rs766444959 Functional Loss SNV dbSNP153 33..33 33 - - - 85256 RMVar_ID_85256 Human_SNP_ID_599679953 m1A Human chr16 + 31081764 31081764 31081764 TGGGCACACAGTGGAGGGGGAAGTCCAGCCCCAAAGTCGGTGGGGGAGCAAGGAGTGAGAGGAGA TGGGCACACAGTGGAGGGGGAAGTCCAGCCCCGAAGTCGGTGGGGGAGCAAGGAGTGAGAGGAGA A G ZNF646 Ensembl:ENSG00000167395 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:31081719..31081911 26863196 MeRIP-seq:(Medium) rs1289849302 Functional Loss SNV dbSNP153 33..33 33 - - - 85257 RMVar_ID_85257 Human_SNP_ID_599682899 m1A Human chr16 + 31091249 31091249 31091249 TGATACAAACAATGCAGAAATCATAGAGCACGAAGAACAGGATCCAGGCCAGGTAGACAGAACCA TGATACAAACAATGCAGAAATCATAGAGCACGGAGAACAGGATCCAGGCCAGGTAGACAGAACCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31090904..31091297 26863196 MeRIP-seq:(Medium) rs1022061765 Functional Loss SNV dbSNP153 33..33 33 - - - 85258 RMVar_ID_85258 Human_SNP_ID_599684012 m1A Human chr16 - 31094723 31094723 31094723 GGCGCCTCGGGCGGAACCTGGAGATAATGGGCAGCACCTGGGGGAGCCCTGGCTGGGTGCGGCTC GGCGCCTCGGGCGGAACCTGGAGATAATGGGCCGCACCTGGGGGAGCCCTGGCTGGGTGCGGCTC T G VKORC1,AC135050.2 Ensembl:ENSG00000167397,Ensembl:ENSG00000255439 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1464695762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233994,Human_RBP_ID_473329,Human_RBP_ID_761783,Human_RBP_ID_818786,Human_RBP_ID_1517248,Human_RBP_ID_4366486,Human_RBP_ID_5141909,Human_RBP_ID_5236608,Human_RBP_ID_5465060,Human_RBP_ID_9325099,Human_RBP_ID_17371434,Human_RBP_ID_17653020,Human_RBP_ID_17875942,Human_RBP_ID_18469908,Human_RBP_ID_22440983,Human_RBP_ID_22497805 Human_miRNA_ID_2469562 RMVar_hsa_circ_78397,RMVar_hsa_circ_178009 85259 RMVar_ID_85259 Human_SNP_ID_599684016 m1A Human chr16 + 31094728 31094728 31094728 GCACCCAGCCAGGGCTCCCCCAGGTGCTGCCCATTATCTCCAGGTTCCGCCCGAGGCGCCCGCGG GCACCCAGCCAGGGCTCCCCCAGGTGCTGCCCGTTATCTCCAGGTTCCGCCCGAGGCGCCCGCGG A G AC135050.7 Ensembl:ENSG00000280160 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31094416..31094959 26863196 MeRIP-seq:(Medium) rs778819991 Functional Loss SNV dbSNP153 33..33 33 - - - 85260 RMVar_ID_85260 Human_SNP_ID_599684031 m1A Human chr16 + 31094749 31094749 31094749 AGGTGCTGCCCATTATCTCCAGGTTCCGCCCGAGGCGCCCGCGGAGAAAACCAGCCACGGAGCAG AGGTGCTGCCCATTATCTCCAGGTTCCGCCCGCGGCGCCCGCGGAGAAAACCAGCCACGGAGCAG A C AC135050.7 Ensembl:ENSG00000280160 Other exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:31094701..31094900;chr16:31094701..31094925 26863196 MeRIP-seq:(Medium) rs1181905560 Functional Loss SNV dbSNP153 33..33 33 - - - 85261 RMVar_ID_85261 Human_SNP_ID_599684045 m1A Human chr16 + 31094769 31094769 31094769 AGGTTCCGCCCGAGGCGCCCGCGGAGAAAACCAGCCACGGAGCAGGGGCCGGGCGGCGAATGGCC AGGTTCCGCCCGAGGCGCCCGCGGAGAAAACCGGCCACGGAGCAGGGGCCGGGCGGCGAATGGCC A G AC135050.7 Ensembl:ENSG00000280160 Other exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:31094718..31094896 26863196 MeRIP-seq:(Medium) rs1438476889 Functional Loss SNV dbSNP153 33..33 33 - - - 85262 RMVar_ID_85262 Human_SNP_ID_599684053 m1A Human chr16 + 31094777 31094777 31094777 CCCGAGGCGCCCGCGGAGAAAACCAGCCACGGAGCAGGGGCCGGGCGGCGAATGGCCGCGCCCCT CCCGAGGCGCCCGCGGAGAAAACCAGCCACGGCGCAGGGGCCGGGCGGCGAATGGCCGCGCCCCT A C AC135050.7 Ensembl:ENSG00000280160 Other exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:31094726..31094925 26863196 MeRIP-seq:(Medium) rs1271265836 Functional Loss SNV dbSNP153 33..33 33 - - - 85263 RMVar_ID_85263 Human_SNP_ID_599687948 m1A Human chr16 + 31109116 31109116 31109116 CCTCGACGCACCCTGGTCCCTGAAGTCGGAGAAGAGCCCCTACCCACCCACACCCCCTTGCCCCA CCTCGACGCACCCTGGTCCCTGAAGTCGGAGAGGAGCCCCTACCCACCCACACCCCCTTGCCCCA A G BCKDK Ensembl:ENSG00000103507 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31109026..31109354 26863196 MeRIP-seq:(Medium) rs894643593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1517253,Human_RBP_ID_4366509 Human_Splice_Rec_1704980,Human_Splice_Rec_1705002,Human_Splice_Rec_1705022,Human_Splice_Rec_1705042,Human_Splice_Rec_1705060,Human_Splice_Rec_1705082,Human_Splice_Rec_1705098 RMVar_hsa_circ_96965,RMVar_hsa_circ_178010 85264 RMVar_ID_85264 Human_SNP_ID_599687980 m1A Human chr16 + 31109211 31109211 31109211 GGATCCTCAGTCCTAGCGGCCACCGGGTCTGAAAGGAGCAAGACGATGATCCTGGCGTCGGTGCT GGATCCTCAGTCCTAGCGGCCACCGGGTCTGAGAGGAGCAAGACGATGATCCTGGCGTCGGTGCT A G BCKDK Ensembl:ENSG00000103507 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:31109160..31109310;chr16:31109160..31109409 32194978 MeRIP-seq:(Medium) rs1288581478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1517254,Human_RBP_ID_4394673,Human_RBP_ID_23687313 Human_miRNA_ID_1264931,Human_miRNA_ID_2611594 RMVar_hsa_circ_96965,RMVar_hsa_circ_178010 85265 RMVar_ID_85265 Human_SNP_ID_599688145 m1A Human chr16 - 31109549 31109549 31109549 ACCAGAAGGTGGCTGCCGTCCTGAGAGCGGCCAGCGTAGAGCATCATGGTGGGCGTTAGGCGGAC ACCAGAAGGTGGCTGCCGTCCTGAGAGCGGCCGGCGTAGAGCATCATGGTGGGCGTTAGGCGGAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31109408..31109842 32194978 MeRIP-seq:(Medium) rs777686530 Functional Loss SNV dbSNP153 33..33 33 - - - 85266 RMVar_ID_85266 Human_SNP_ID_599688226 m1A Human chr16 + 31109779 31109779 31109779 TTTCATCATTGGCTGCAACCCCACCATACTGCACGTGGTAAGGTAGAGAGGACCTTAGGTCAGCG TTTCATCATTGGCTGCAACCCCACCATACTGCGCGTGGTAAGGTAGAGAGGACCTTAGGTCAGCG A G BCKDK Ensembl:ENSG00000103507 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31109660..31109800 26863196 MeRIP-seq:(Medium) rs1440367751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_890553,Human_RBP_ID_18986182,Human_RBP_ID_19074244,Human_RBP_ID_26810307 Human_Splice_Rec_1704985,Human_Splice_Rec_1705007,Human_Splice_Rec_1705027,Human_Splice_Rec_1705047,Human_Splice_Rec_1705065,Human_Splice_Rec_1705105 RMVar_hsa_circ_17173,RMVar_hsa_circ_96965,RMVar_hsa_circ_178010,RMVar_hsa_circ_33165,RMVar_hsa_circ_69910,RMVar_hsa_circ_370764,RMVar_hsa_circ_178011 85267 RMVar_ID_85267 Human_SNP_ID_599688426 m1A Human chr16 - 31110326 31110326 31110326 CCAGCAGGCCCGGCCTCTCCTTTGCTGCCCCAACCTCTATGTGCTTCCGGCTCTCACGTAGGCCC CCAGCAGGCCCGGCCTCTCCTTTGCTGCCCCATCCTCTATGTGCTTCCGGCTCTCACGTAGGCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31110219..31110445 32194978 MeRIP-seq:(Medium) rs1567428829 Functional Loss SNV dbSNP153 33..33 33 - - - 85268 RMVar_ID_85268 Human_SNP_ID_599689204 m1A Human chr16 - 31112642 31112642 31112642 GCAGGTAAGAGACTGGGACACGAACCAGTTCAACCCAAGGGCTCAGTGAACCTGAATGGGGGCAG GCAGGTAAGAGACTGGGACACGAACCAGTTCATCCCAAGGGCTCAGTGAACCTGAATGGGGGCAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31112591..31112692 32194978 MeRIP-seq:(Medium) rs761995044 Functional Loss SNV dbSNP153 33..33 33 - - - 85269 RMVar_ID_85269 Human_SNP_ID_599690773 m1A Human chr16 + 31117781 31117781 31117781 CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGACCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGCCCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG A C KAT8 Ensembl:ENSG00000103510 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31117732..31117846 26863196 MeRIP-seq:(Medium) rs1030164303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393063,Human_RBP_ID_9325101,Human_RBP_ID_22441490,Human_RBP_ID_22532818,Human_RBP_ID_24552072,Human_RBP_ID_26769135 RMVar_hsa_circ_64374 85270 RMVar_ID_85270 Human_SNP_ID_599690774 m1A Human chr16 + 31117781 31117781 31117781 CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGACCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGGCCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG A G KAT8 Ensembl:ENSG00000103510 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31117732..31117846 26863196 MeRIP-seq:(Medium) rs1030164303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393063,Human_RBP_ID_9325101,Human_RBP_ID_22441490,Human_RBP_ID_22532818,Human_RBP_ID_24552072,Human_RBP_ID_26769135 RMVar_hsa_circ_64374 85271 RMVar_ID_85271 Human_SNP_ID_599690833 m1A Human chr16 + 31117927 31117927 31117927 GAGGGCGGGGCCCAGGGCTGGGGGCGGGGCGGAGCTCAGGGCCAGGGGGTGGGGCGGGGCCTGAG GAGGGCGGGGCCCAGGGCTGGGGGCGGGGCGGGGCTCAGGGCCAGGGGGTGGGGCGGGGCCTGAG A G KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31117923..31118045 26863196 MeRIP-seq:(Medium) rs1337048430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8184540,Human_RBP_ID_9419210,Human_RBP_ID_26780396 RMVar_hsa_circ_64374 85272 RMVar_ID_85272 Human_SNP_ID_599693131 m1A Human chr16 + 31126187 31126187 31126187 TGCTGGCAGTGAGAGAAGGAAGGGCATTCTCCAGGTAGAAGGAGCTGTTTGTGCAGAAGCATGAA TGCTGGCAGTGAGAGAAGGAAGGGCATTCTCCCGGTAGAAGGAGCTGTTTGTGCAGAAGCATGAA A C KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:31126186..31126364 26863196 MeRIP-seq:(Medium) rs1028458557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509128,Human_RBP_ID_12724116 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 85273 RMVar_ID_85273 Human_SNP_ID_599693176 m1A Human chr16 + 31126371 31126371 31126371 AGAGAGGAGAATTCCAGAGAGGGCCCAATTCCAGAGATGTCAGAAGTAGACTCGACATCCACTGT AGAGAGGAGAATTCCAGAGAGGGCCCAATTCCGGAGATGTCAGAAGTAGACTCGACATCCACTGT A G KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31126369..31126467 26863196 MeRIP-seq:(Medium) rs112491351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12724121 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 85274 RMVar_ID_85274 Human_SNP_ID_599694579 m1A Human chr16 + 31131212 31131212 31131212 CCCTTCTCCCCACAGTGGACTCCGTCTGCCTCAAGTGGGCACCCCCCAAGCACAAGCAAGTCAAG CCCTTCTCCCCACAGTGGACTCCGTCTGCCTCGAGTGGGCACCCCCCAAGCACAAGCAAGTCAAG A G KAT8 Ensembl:ENSG00000103510 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31131193..31131293 32194978 MeRIP-seq:(Medium) rs1291615619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473390,Human_RBP_ID_892040,Human_RBP_ID_22497813 Human_Splice_Rec_1705142,Human_Splice_Rec_1705180,Human_Splice_Rec_1705198,Human_Splice_Rec_1705208 Human_miRNA_ID_1038956 85275 RMVar_ID_85275 Human_SNP_ID_599694997 m1A Human chr16 + 31132543 31132543 31132543 TCGATGTTGTACAGGCAGTTACACGTCTCACGACTGATCAGAGGCACCTCGAGTTGCTGCAGTGG TCGATGTTGTACAGGCAGTTACACGTCTCACGGCTGATCAGAGGCACCTCGAGTTGCTGCAGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31132492..31132568 26863196 MeRIP-seq:(Medium) rs750425055 Functional Loss SNV dbSNP153 33..33 33 - - - 85276 RMVar_ID_85276 Human_SNP_ID_599708561 m1A Human chr16 + 31180161 31180161 31180161 AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTACTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTGCTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG A G FUS Ensembl:ENSG00000089280 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs929867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473397,Human_RBP_ID_763399,Human_RBP_ID_816457,Human_RBP_ID_1517294,Human_RBP_ID_1841782,Human_RBP_ID_4393799,Human_RBP_ID_5180679,Human_RBP_ID_5419257,Human_RBP_ID_5440470,Human_RBP_ID_5465893,Human_RBP_ID_8432726,Human_RBP_ID_9372734,Human_RBP_ID_18678318,Human_RBP_ID_22440986,Human_RBP_ID_26440974,Human_RBP_ID_26944095,Human_RBP_ID_27658010 Human_Splice_Rec_1705375,Human_Splice_Rec_1705401,Human_Splice_Rec_1705405,Human_Splice_Rec_1705433,Human_Splice_Rec_1705461,Human_Splice_Rec_1705485 Clinvar_Rec_445 85277 RMVar_ID_85277 Human_SNP_ID_599708562 m1A Human chr16 + 31180161 31180161 31180161 AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTACTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTTCTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG A T FUS Ensembl:ENSG00000089280 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs929867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473397,Human_RBP_ID_763399,Human_RBP_ID_816457,Human_RBP_ID_1517294,Human_RBP_ID_1841782,Human_RBP_ID_4393799,Human_RBP_ID_5180679,Human_RBP_ID_5419257,Human_RBP_ID_5440470,Human_RBP_ID_5465893,Human_RBP_ID_8432726,Human_RBP_ID_9372734,Human_RBP_ID_18678318,Human_RBP_ID_22440986,Human_RBP_ID_26440974,Human_RBP_ID_26944095,Human_RBP_ID_27658010 Human_Splice_Rec_1705375,Human_Splice_Rec_1705401,Human_Splice_Rec_1705405,Human_Splice_Rec_1705433,Human_Splice_Rec_1705461,Human_Splice_Rec_1705485 Clinvar_Rec_445 85278 RMVar_ID_85278 Human_SNP_ID_599708619 m1A Human chr16 - 31180196 31180196 31180196 CCGTTTGAGGCCATGTCCGCGCACGCGCGCACAGGCAAGCAAGCAACGAAGTTCCAACACCGCTG CCGTTTGAGGCCATGTCCGCGCACGCGCGCACGGGCAAGCAAGCAACGAAGTTCCAACACCGCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31180151..31180350 26863196 MeRIP-seq:(Medium) rs1567467403 Functional Loss SNV dbSNP153 33..33 33 - - - 85279 RMVar_ID_85279 Human_SNP_ID_599708774 m1A Human chr16 - 31180537 31180537 31180537 CTCGAGCGCGGGGCCGGGAGTTGGGGGAGGCGAGGCCACGGAGAATGGGCGTTTTCCACCCTCAC CTCGAGCGCGGGGCCGGGAGTTGGGGGAGGCGGGGCCACGGAGAATGGGCGTTTTCCACCCTCAC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31180501..31180700 26863196 MeRIP-seq:(Medium) rs1195804060 Functional Loss SNV dbSNP153 33..33 33 - - - 85280 RMVar_ID_85280 Human_SNP_ID_599709585 m1A Human chr16 - 31182564 31182564 31182564 TAACCACTGTAACTCTGCTGTCCGTAGGGCTGACTGCTCTGCTGGGAATAGCCCTGCCCGGGCTG TAACCACTGTAACTCTGCTGTCCGTAGGGCTGGCTGCTCTGCTGGGAATAGCCCTGCCCGGGCTG T C AC009088.2 Ensembl:ENSG00000260304 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr16:31182429..31182575;chr16:31182429..31182566;chr16:31182501..31182575;chr16:31182458..31182717;chr16:31180151..31182675 26863196,32194978 MeRIP-seq:(Medium) rs1485377976 Functional Loss SNV dbSNP153 33..33 33 - - - 85281 RMVar_ID_85281 Human_SNP_ID_599709605 m1A Human chr16 + 31182618 31182618 31182618 TACAGTGGTTATAGCCAGTCCACGGACACTTCAGGCTATGGCCAGAGCAGCTATTCTTCTTATGG TACAGTGGTTATAGCCAGTCCACGGACACTTCGGGCTATGGCCAGAGCAGCTATTCTTCTTATGG A G FUS Ensembl:ENSG00000089280 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31182487..31182707 26863196 MeRIP-seq:(Medium) rs80060438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1177916,Human_RBP_ID_1517314,Human_RBP_ID_4394680,Human_RBP_ID_5184254,Human_RBP_ID_6509168,Human_RBP_ID_9374263,Human_RBP_ID_12873870,Human_RBP_ID_18437614,Human_RBP_ID_18678328,Human_RBP_ID_22201395,Human_RBP_ID_22421640,Human_RBP_ID_22442511,Human_RBP_ID_26446723,Human_RBP_ID_26810318,Human_RBP_ID_26944106,Human_RBP_ID_27241386 Human_Splice_Rec_1705379,Human_Splice_Rec_1705409,Human_Splice_Rec_1705437,Human_Splice_Rec_1705465,Human_Splice_Rec_1705489 Human_miRNA_ID_2393606,Human_miRNA_ID_2908264,Human_miRNA_ID_3027103 GWAS_ID_10153,GWAS_ID_10154 RMVar_hsa_circ_10497,RMVar_hsa_circ_178021,RMVar_hsa_circ_376384,RMVar_hsa_circ_375552,RMVar_hsa_circ_178022 85282 RMVar_ID_85282 Human_SNP_ID_599710264 m1A Human chr16 + 31184305 31184305 31184305 CCTAGCTATGGTGGACAGCAGCAAAGCTATGGACAGCAGCAAAGCTATAATCCCCCTCAGGGCTA CCTAGCTATGGTGGACAGCAGCAAAGCTATGGGCAGCAGCAAAGCTATAATCCCCCTCAGGGCTA A G FUS Ensembl:ENSG00000089280 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31184255..31184406 26863196 MeRIP-seq:(Medium) rs779527448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43897,Human_RBP_ID_1517336,Human_RBP_ID_1841805,Human_RBP_ID_3494454,Human_RBP_ID_4366713,Human_RBP_ID_6509206,Human_RBP_ID_12724405,Human_RBP_ID_18678342,Human_RBP_ID_22759843,Human_RBP_ID_26328141,Human_RBP_ID_27241397,Human_RBP_ID_27811075 Human_Splice_Rec_1705382,Human_Splice_Rec_1705383,Human_Splice_Rec_1705412,Human_Splice_Rec_1705413,Human_Splice_Rec_1705440,Human_Splice_Rec_1705441,Human_Splice_Rec_1705468,Human_Splice_Rec_1705469,Human_Splice_Rec_1705492,Human_Splice_Rec_1705493,Human_Splice_Rec_1705514 RMVar_hsa_circ_18715,RMVar_hsa_circ_103740,RMVar_hsa_circ_69719,RMVar_hsa_circ_178023,RMVar_hsa_circ_178024,RMVar_hsa_circ_377993 85283 RMVar_ID_85283 Human_SNP_ID_599710644 m1A Human chr16 + 31185038 31185038 31185038 AGACCAGAGTGGTGGAGGTGGCAGCGGTGGCTATGGACAGCAGGACCGTGGAGGCCGCGGCAGGG AGACCAGAGTGGTGGAGGTGGCAGCGGTGGCTGTGGACAGCAGGACCGTGGAGGCCGCGGCAGGG A G FUS Ensembl:ENSG00000089280 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:31184170..31185361;chr16:31184301..31185231 26863196 MeRIP-seq:(Medium) rs1424075127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234605,Human_RBP_ID_816614,Human_RBP_ID_894064,Human_RBP_ID_2473371,Human_RBP_ID_3947613,Human_RBP_ID_4366720,Human_RBP_ID_8432749,Human_RBP_ID_9353213,Human_RBP_ID_12724418,Human_RBP_ID_18986209,Human_RBP_ID_22421647,Human_RBP_ID_22426232,Human_RBP_ID_22441998,Human_RBP_ID_22801375,Human_RBP_ID_22945053,Human_RBP_ID_23128166,Human_RBP_ID_26328957,Human_RBP_ID_26944128,Human_RBP_ID_27837844 Human_Splice_Rec_1705384,Human_Splice_Rec_1705414,Human_Splice_Rec_1705442,Human_Splice_Rec_1705470,Human_Splice_Rec_1705494 Human_miRNA_ID_2512748,Human_miRNA_ID_3055571 RMVar_hsa_circ_18715,RMVar_hsa_circ_69719,RMVar_hsa_circ_178025,RMVar_hsa_circ_178027,RMVar_hsa_circ_376838 85284 RMVar_ID_85284 Human_SNP_ID_599710668 m1A Human chr16 - 31185078 31185075 31185078 TAACCACCACCGCCGCCGCCGCCGCCGCCACCACTGCCACCCCTGCCGCGGCCTCCACGGTCCTG TAACCACCACCGCCGCCGCCGCCGCCGCCACC___GCCACCCCTGCCGCGGCCTCCACGGTCCTG CAGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:31185000..31185212 26863196 MeRIP-seq:(Medium) rs746633090 Functional Loss DEL dbSNP153 33..35 33 - - - Clinvar_Rec_446 85285 RMVar_ID_85285 Human_SNP_ID_599710672 m1A Human chr16 - 31185078 31185076 31185079 TAACCACCACCGCCGCCGCCGCCGCCGCCACCACTGCCACCCCTGCCGCGGCCTCCACGGTCCTG TAACCACCACCGCCGCCGCCGCCGCCGCCAC___TGCCACCCCTGCCGCGGCCTCCACGGTCCTG AGTG A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:31185000..31185212 26863196 MeRIP-seq:(Medium) rs774111102 Functional Loss DEL dbSNP153 32..34 33 - - - 85286 RMVar_ID_85286 Human_SNP_ID_599710757 m1A Human chr16 + 31185175 31185175 31185175 GTCGTGGAGGTGGCCGTGGAGGCAGAGGTGGCATGGGGTAGGTGTCTCATGAGCCAGGGAGTATC GTCGTGGAGGTGGCCGTGGAGGCAGAGGTGGCGTGGGGTAGGTGTCTCATGAGCCAGGGAGTATC A G FUS Ensembl:ENSG00000089280 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31184951..31185255 26863196 MeRIP-seq:(Medium) rs752076094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473401,Human_RBP_ID_763152,Human_RBP_ID_816804,Human_RBP_ID_2492180,Human_RBP_ID_5355827,Human_RBP_ID_8086960,Human_RBP_ID_8432750,Human_RBP_ID_9353217,Human_RBP_ID_12724426,Human_RBP_ID_17652635,Human_RBP_ID_18544345,Human_RBP_ID_19074261,Human_RBP_ID_21973081,Human_RBP_ID_22440990,Human_RBP_ID_22474157,Human_RBP_ID_22801378,Human_RBP_ID_22945054,Human_RBP_ID_26328958,Human_RBP_ID_27837845 Human_Splice_Rec_1705385,Human_Splice_Rec_1705415,Human_Splice_Rec_1705443,Human_Splice_Rec_1705495,Human_Splice_Rec_1705515 GWAS_ID_10155,GWAS_ID_10156 RMVar_hsa_circ_18715,RMVar_hsa_circ_69719,RMVar_hsa_circ_178025 85287 RMVar_ID_85287 Human_SNP_ID_599711987 m1A Human chr16 - 31189103 31189101 31189103 GAATTATCCTGTTCTGCTTGTTGAACAGAGAAAATGCAAATGTGAAAAGGTAAAATAAAAAACAC GAATTATCCTGTTCTGCTTGTTGAACAGAGAA__TGCAAATGTGAAAAGGTAAAATAAAAAACAC ATT A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:31189101..31189125;chr16:31189101..31189250;chr16:31189101..31189150 26863196 MeRIP-seq:(Medium) rs760802136 Functional Loss DEL dbSNP153 33..34 33 - - - 85288 RMVar_ID_85288 Human_SNP_ID_599712014 m1A Human chr16 - 31189228 31189228 31189228 CTGACAGAAAGCTCCCACTCCTCTCCACAAGTACCTTAATAATACCAATCTGCTTGAAGTAATCA CTGACAGAAAGCTCCCACTCCTCTCCACAAGTTCCTTAATAATACCAATCTGCTTGAAGTAATCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31189201..31189250 26863196 MeRIP-seq:(Medium) rs112462091 Functional Loss SNV dbSNP153 33..33 33 - - - 85289 RMVar_ID_85289 Human_SNP_ID_599712015 m1A Human chr16 - 31189228 31189228 31189228 CTGACAGAAAGCTCCCACTCCTCTCCACAAGTACCTTAATAATACCAATCTGCTTGAAGTAATCA CTGACAGAAAGCTCCCACTCCTCTCCACAAGTGCCTTAATAATACCAATCTGCTTGAAGTAATCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31189201..31189250 26863196 MeRIP-seq:(Medium) rs112462091 Functional Loss SNV dbSNP153 33..33 33 - - - 85290 RMVar_ID_85290 Human_SNP_ID_599712161 m1A Human chr16 + 31189715 31189715 31189715 CAGCCCATGATTAATTTGTACACAGACAGGGAAACTGGCAAGCTGAAGGGAGAGGCAACGGTCTC CAGCCCATGATTAATTTGTACACAGACAGGGACACTGGCAAGCTGAAGGGAGAGGCAACGGTCTC A C FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31189638..31189804 26863196 MeRIP-seq:(Medium) rs1452330341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46015,Human_RBP_ID_1517465,Human_RBP_ID_1841866,Human_RBP_ID_3494491,Human_RBP_ID_4366819,Human_RBP_ID_5576721,Human_RBP_ID_6509362,Human_RBP_ID_8432831,Human_RBP_ID_9061930,Human_RBP_ID_9372741,Human_RBP_ID_12724734,Human_RBP_ID_18162975,Human_RBP_ID_22421652,Human_RBP_ID_22801409,Human_RBP_ID_22939016,Human_RBP_ID_25207549,Human_RBP_ID_26944200 Human_Splice_Rec_1705390,Human_Splice_Rec_1705391,Human_Splice_Rec_1705422,Human_Splice_Rec_1705423,Human_Splice_Rec_1705450,Human_Splice_Rec_1705451,Human_Splice_Rec_1705474,Human_Splice_Rec_1705475,Human_Splice_Rec_1705502,Human_Splice_Rec_1705503,Human_Splice_Rec_1705524,Human_Splice_Rec_1705525,Human_Splice_Rec_1705536,Human_Splice_Rec_1705537,Human_Splice_Rec_1705540 RMVar_hsa_circ_5336,RMVar_hsa_circ_37053 85291 RMVar_ID_85291 Human_SNP_ID_599712323 m1A Human chr16 + 31190140 31190140 31190140 GGTGGCAATGGTCGTGGAGGCCGAGGGCGAGGAGGTGAGGAGCTACCTGCTAGTGGTGCAGAGGG GGTGGCAATGGTCGTGGAGGCCGAGGGCGAGGTGGTGAGGAGCTACCTGCTAGTGGTGCAGAGGG A T FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr16:31190051..31190428;chr16:31190101..31190150 26863196 MeRIP-seq:(Medium) rs1381085895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816617,Human_RBP_ID_5358066,Human_RBP_ID_9286281,Human_RBP_ID_9353218,Human_RBP_ID_9372744,Human_RBP_ID_18986210,Human_RBP_ID_22440994,Human_RBP_ID_23118463,Human_RBP_ID_27837850 Human_Splice_Rec_1705393,Human_Splice_Rec_1705425,Human_Splice_Rec_1705453,Human_Splice_Rec_1705477,Human_Splice_Rec_1705505,Human_Splice_Rec_1705527 RMVar_hsa_circ_5336,RMVar_hsa_circ_37053,RMVar_hsa_circ_267053 85292 RMVar_ID_85292 Human_SNP_ID_599712400 m1A Human chr16 + 31190340 31190340 31190340 GCAGTGGTGGTGGTGGCCGAGGAGGATTTCCCAGTGGAGGTGGTGGCGGTGGAGGACAGCAGCGA GCAGTGGTGGTGGTGGCCGAGGAGGATTTCCCGGTGGAGGTGGTGGCGGTGGAGGACAGCAGCGA A G FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:31190156..31190400 26863196 MeRIP-seq:(Medium) rs771912107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5772,Human_RBP_ID_46018,Human_RBP_ID_234616,Human_RBP_ID_473409,Human_RBP_ID_763414,Human_RBP_ID_816805,Human_RBP_ID_1004275,Human_RBP_ID_3947615,Human_RBP_ID_4399825,Human_RBP_ID_5524428,Human_RBP_ID_5571717,Human_RBP_ID_6509376,Human_RBP_ID_8807446,Human_RBP_ID_9353220,Human_RBP_ID_9372745,Human_RBP_ID_17652645,Human_RBP_ID_17876007,Human_RBP_ID_18162979,Human_RBP_ID_18437631,Human_RBP_ID_18983721,Human_RBP_ID_19071484,Human_RBP_ID_22421655,Human_RBP_ID_22440996,Human_RBP_ID_22739373,Human_RBP_ID_22801414,Human_RBP_ID_22939029,Human_RBP_ID_23128174,Human_RBP_ID_23687590,Human_RBP_ID_26328963,Human_RBP_ID_26944205,Human_RBP_ID_27241432,Human_RBP_ID_27811076,Human_RBP_ID_27837852 Human_Splice_Rec_1705394,Human_Splice_Rec_1705395,Human_Splice_Rec_1705426,Human_Splice_Rec_1705427,Human_Splice_Rec_1705454,Human_Splice_Rec_1705455,Human_Splice_Rec_1705478,Human_Splice_Rec_1705479,Human_Splice_Rec_1705506,Human_Splice_Rec_1705507,Human_Splice_Rec_1705528,Human_Splice_Rec_1705529,Human_Splice_Rec_1705541 Human_miRNA_ID_208276,Human_miRNA_ID_2969415 RMVar_hsa_circ_5336,RMVar_hsa_circ_377725,RMVar_hsa_circ_267053,RMVar_hsa_circ_178029 85293 RMVar_ID_85293 Human_SNP_ID_599712408 m1A Human chr16 + 31190363 31190363 31190363 GGATTTCCCAGTGGAGGTGGTGGCGGTGGAGGACAGCAGCGAGCTGGTGACTGGAAGTGTCCTAA GGATTTCCCAGTGGAGGTGGTGGCGGTGGAGGGCAGCAGCGAGCTGGTGACTGGAAGTGTCCTAA A G FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:31190133..31190374;chr16:31189101..31190433;chr16:31190051..31190450 26863196 MeRIP-seq:(Medium) rs1405307150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5772,Human_RBP_ID_46018,Human_RBP_ID_234616,Human_RBP_ID_473409,Human_RBP_ID_763414,Human_RBP_ID_816805,Human_RBP_ID_3947615,Human_RBP_ID_4399825,Human_RBP_ID_5524428,Human_RBP_ID_6509376,Human_RBP_ID_8807447,Human_RBP_ID_9353220,Human_RBP_ID_9372745,Human_RBP_ID_17002159,Human_RBP_ID_17652645,Human_RBP_ID_18162980,Human_RBP_ID_18983721,Human_RBP_ID_19071484,Human_RBP_ID_22421655,Human_RBP_ID_22440996,Human_RBP_ID_22739373,Human_RBP_ID_22939030,Human_RBP_ID_23128175,Human_RBP_ID_23687590,Human_RBP_ID_26328963,Human_RBP_ID_27811076,Human_RBP_ID_27837853 Human_Splice_Rec_1705394,Human_Splice_Rec_1705395,Human_Splice_Rec_1705426,Human_Splice_Rec_1705427,Human_Splice_Rec_1705454,Human_Splice_Rec_1705455,Human_Splice_Rec_1705478,Human_Splice_Rec_1705479,Human_Splice_Rec_1705506,Human_Splice_Rec_1705507,Human_Splice_Rec_1705528,Human_Splice_Rec_1705529,Human_Splice_Rec_1705541 RMVar_hsa_circ_5336,RMVar_hsa_circ_267053 85294 RMVar_ID_85294 Human_SNP_ID_599712717 m1A Human chr16 + 31191100 31191100 31191100 GTGGGGACAGAGGTGGCTTTGGCCCTGGCAAGATGGATTCCAGGTAAGACTTTAAATCAGAATAA GTGGGGACAGAGGTGGCTTTGGCCCTGGCAAGGTGGATTCCAGGTAAGACTTTAAATCAGAATAA A G FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:31191001..31191152 26863410 MeRIP-seq:(Medium) rs771109274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5773,Human_RBP_ID_234619,Human_RBP_ID_763418,Human_RBP_ID_816621,Human_RBP_ID_3947619,Human_RBP_ID_5113500,Human_RBP_ID_5141912,Human_RBP_ID_5317547,Human_RBP_ID_5524430,Human_RBP_ID_8432845,Human_RBP_ID_9353221,Human_RBP_ID_9444026,Human_RBP_ID_12724779,Human_RBP_ID_17652647,Human_RBP_ID_17690197,Human_RBP_ID_18162112,Human_RBP_ID_18983725,Human_RBP_ID_19071487,Human_RBP_ID_22426233,Human_RBP_ID_22442006,Human_RBP_ID_22654200,Human_RBP_ID_24369438,Human_RBP_ID_24551923,Human_RBP_ID_26328967,Human_RBP_ID_26769136,Human_RBP_ID_27837855 Human_Splice_Rec_1705399,Human_Splice_Rec_1705431,Human_Splice_Rec_1705459,Human_Splice_Rec_1705483,Human_Splice_Rec_1705511,Human_Splice_Rec_1705545,Human_Splice_Rec_1705549 RMVar_hsa_circ_29352,RMVar_hsa_circ_178030 85295 RMVar_ID_85295 Human_SNP_ID_599712720 m1A Human chr16 + 31191109 31191109 31191109 GAGGTGGCTTTGGCCCTGGCAAGATGGATTCCAGGTAAGACTTTAAATCAGAATAAAAAAGTAGA GAGGTGGCTTTGGCCCTGGCAAGATGGATTCCCGGTAAGACTTTAAATCAGAATAAAAAAGTAGA A C FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr16:31190951..31191125;chr16:31190940..31191150 26863196 MeRIP-seq:(Medium) rs1555509609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816621,Human_RBP_ID_3947619,Human_RBP_ID_5113500,Human_RBP_ID_5141912,Human_RBP_ID_5317547,Human_RBP_ID_5524430,Human_RBP_ID_9353221,Human_RBP_ID_9444026,Human_RBP_ID_12724779,Human_RBP_ID_17653025,Human_RBP_ID_17690197,Human_RBP_ID_17883480,Human_RBP_ID_18162112,Human_RBP_ID_18983725,Human_RBP_ID_19071487,Human_RBP_ID_22426233,Human_RBP_ID_22442006,Human_RBP_ID_22654200,Human_RBP_ID_24369438,Human_RBP_ID_24551923,Human_RBP_ID_26328968,Human_RBP_ID_26769136,Human_RBP_ID_27658062 Human_Splice_Rec_1705399,Human_Splice_Rec_1705431,Human_Splice_Rec_1705459,Human_Splice_Rec_1705483,Human_Splice_Rec_1705511,Human_Splice_Rec_1705545,Human_Splice_Rec_1705549 RMVar_hsa_circ_29352,RMVar_hsa_circ_178030 85296 RMVar_ID_85296 Human_SNP_ID_599712721 m1A Human chr16 + 31191109 31191109 31191109 GAGGTGGCTTTGGCCCTGGCAAGATGGATTCCAGGTAAGACTTTAAATCAGAATAAAAAAGTAGA GAGGTGGCTTTGGCCCTGGCAAGATGGATTCCGGGTAAGACTTTAAATCAGAATAAAAAAGTAGA A G FUS Ensembl:ENSG00000089280 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr16:31190951..31191125;chr16:31190940..31191150 26863196 MeRIP-seq:(Medium) rs1555509609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816621,Human_RBP_ID_3947619,Human_RBP_ID_5113500,Human_RBP_ID_5141912,Human_RBP_ID_5317547,Human_RBP_ID_5524430,Human_RBP_ID_9353221,Human_RBP_ID_9444026,Human_RBP_ID_12724779,Human_RBP_ID_17653025,Human_RBP_ID_17690197,Human_RBP_ID_17883480,Human_RBP_ID_18162112,Human_RBP_ID_18983725,Human_RBP_ID_19071487,Human_RBP_ID_22426233,Human_RBP_ID_22442006,Human_RBP_ID_22654200,Human_RBP_ID_24369438,Human_RBP_ID_24551923,Human_RBP_ID_26328968,Human_RBP_ID_26769136,Human_RBP_ID_27658062 Human_Splice_Rec_1705399,Human_Splice_Rec_1705431,Human_Splice_Rec_1705459,Human_Splice_Rec_1705483,Human_Splice_Rec_1705511,Human_Splice_Rec_1705545,Human_Splice_Rec_1705549 RMVar_hsa_circ_29352,RMVar_hsa_circ_178030 85297 RMVar_ID_85297 Human_SNP_ID_599712841 m1A Human chr16 - 31191378 31191376 31191378 CTGTGCTCACCCCTGCAAAAAAAAAAAAAAAAATTAAGTATCCATTATATTTGAGTTACCAGCCT CTGTGCTCACCCCTGCAAAAAAAAAAAAAAAA__TAAGTATCCATTATATTTGAGTTACCAGCCT AAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31191376..31191425 26863196 MeRIP-seq:(Medium) rs1567478963 Functional Loss DEL dbSNP153 33..34 33 - - - 85298 RMVar_ID_85298 Human_SNP_ID_599712843 m1A Human chr16 - 31191381 31191377 31191381 TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAAAAAATTAAGTATCCATTATATTTGAGTTACCAG TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAA____TTAAGTATCCATTATATTTGAGTTACCAG ATTTT A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31191376..31191400 26863196 MeRIP-seq:(Medium) rs371057360 Functional Loss DEL dbSNP153 33..36 33 - - - 85299 RMVar_ID_85299 Human_SNP_ID_599712844 m1A Human chr16 - 31191381 31191377 31191381 TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAAAAAATTAAGTATCCATTATATTTGAGTTACCAG TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAA___ATTAAGTATCCATTATATTTGAGTTACCAG ATTTT AT - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31191376..31191400 26863196 MeRIP-seq:(Medium) rs371057360 Functional Loss DEL dbSNP153 33..35 33 - - - 85300 RMVar_ID_85300 Human_SNP_ID_599712845 m1A Human chr16 - 31191381 31191377 31191381 TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAAAAAATTAAGTATCCATTATATTTGAGTTACCAG TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAA__AATTAAGTATCCATTATATTTGAGTTACCAG ATTTT ATT - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31191376..31191400 26863196 MeRIP-seq:(Medium) rs371057360 Functional Loss DEL dbSNP153 33..34 33 - - - 85301 RMVar_ID_85301 Human_SNP_ID_599712846 m1A Human chr16 - 31191381 31191377 31191381 TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAAAAAATTAAGTATCCATTATATTTGAGTTACCAG TGTCTGTGCTCACCCCTGCAAAAAAAAAAAAA_AAATTAAGTATCCATTATATTTGAGTTACCAG ATTTT ATTT - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31191376..31191400 26863196 MeRIP-seq:(Medium) rs371057360 Functional Loss DEL dbSNP153 33..33 33 - - - 85302 RMVar_ID_85302 Human_SNP_ID_599712935 m1A Human chr16 - 31191501 31191501 31191501 CCTTGGGTGATCAGGAATTGGAAGGTTACAAAATAACGAGGGTAACACTGGGTACAGGACAAAAA CCTTGGGTGATCAGGAATTGGAAGGTTACAAAGTAACGAGGGTAACACTGGGTACAGGACAAAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31191451..31191500 32194978 MeRIP-seq:(Medium) rs746723164 Functional Loss SNV dbSNP153 33..33 33 - - - 85303 RMVar_ID_85303 Human_SNP_ID_599712936 m1A Human chr16 - 31191502 31191502 31191502 CCCTTGGGTGATCAGGAATTGGAAGGTTACAAAATAACGAGGGTAACACTGGGTACAGGACAAAA CCCTTGGGTGATCAGGAATTGGAAGGTTACAAGATAACGAGGGTAACACTGGGTACAGGACAAAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31191401..31191527 32194978 MeRIP-seq:(Medium) rs756928637 Functional Loss SNV dbSNP153 33..33 33 - - - 85304 RMVar_ID_85304 Human_SNP_ID_599712937 m1A Human chr16 - 31191502 31191502 31191502 CCCTTGGGTGATCAGGAATTGGAAGGTTACAAAATAACGAGGGTAACACTGGGTACAGGACAAAA CCCTTGGGTGATCAGGAATTGGAAGGTTACAACATAACGAGGGTAACACTGGGTACAGGACAAAA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31191401..31191527 32194978 MeRIP-seq:(Medium) rs756928637 Functional Loss SNV dbSNP153 33..33 33 - - - 85305 RMVar_ID_85305 Human_SNP_ID_599778146 m1A Human chr16 + 31427816 31427816 31427816 TCGTAGCCCGTGGGCAGAGGGTTCACGTGGCTATTGTGGAACAGAGTGTGGTTGCCGTCCCCCCA TCGTAGCCCGTGGGCAGAGGGTTCACGTGGCTGTTGTGGAACAGAGTGTGGTTGCCGTCCCCCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31427765..31427867 26863196 MeRIP-seq:(Medium) rs780096153 Functional Loss SNV dbSNP153 33..33 33 - - - 85306 RMVar_ID_85306 Human_SNP_ID_599782268 m1A Human chr16 + 31443096 31443096 31443096 CCAACCCCTCCACTCCCTGACCAGGATGAGGGAGTCCGCGCCATGCGCATGCACACACGCGGGCC CCAACCCCTCCACTCCCTGACCAGGATGAGGGGGTCCGCGCCATGCGCATGCACACACGCGGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31443070..31443292 26863196 MeRIP-seq:(Medium) rs1199128615 Functional Loss SNV dbSNP153 33..33 33 - - - 85307 RMVar_ID_85307 Human_SNP_ID_599786795 m1A Human chr16 - 31459142 31459142 31459142 CGTGCCCCGCCCCCGGCGTGCACTCGGCGGGGACCGCCTTTTCTCCTCTAGGCTCGCTTCGCTGC CGTGCCCCGCCCCCGGCGTGCACTCGGCGGGGGCCGCCTTTTCTCCTCTAGGCTCGCTTCGCTGC T C AC026471.1 Ensembl:ENSG00000260267 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:31459058..31459252 26863196 MeRIP-seq:(Medium) rs1411281396 Functional Loss SNV dbSNP153 33..33 33 - - - 85308 RMVar_ID_85308 Human_SNP_ID_599787056 m1A Human chr16 - 31459604 31459604 31459604 TCTCGTTGGTCGCTGGGTCCTTTTCCCCACCCAGAGCCTCCCCGGCCGCCGCCGCGAGCTGCGCG TCTCGTTGGTCGCTGGGTCCTTTTCCCCACCCGGAGCCTCCCCGGCCGCCGCCGCGAGCTGCGCG T C AC026471.1 Ensembl:ENSG00000260267 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31459555..31459621 26863196 MeRIP-seq:(Medium) rs753738233 Functional Loss SNV dbSNP153 33..33 33 - - - 85309 RMVar_ID_85309 Human_SNP_ID_599790982 m1A Human chr16 - 31472203 31472203 31472203 GGGGCCACGGACCCGGGGATCCGGCCCCACTCACCCAGGTCCTCCATGGCGGGGCGCGGGCCGGT GGGGCCACGGACCCGGGGATCCGGCCCCACTCCCCCAGGTCCTCCATGGCGGGGCGCGGGCCGGT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:31472180..31472325 26863196 MeRIP-seq:(Medium) rs1220048430 Functional Loss SNV dbSNP153 33..33 33 - - - 85310 RMVar_ID_85310 Human_SNP_ID_599791340 m1A Human chr16 + 31473524 31473524 31473524 GGGCTCCCAAAGAGCGCCCTGCGGAGCCTCTCACCCCTCCCCCATCCTATGGCCACCAGCCACAG GGGCTCCCAAAGAGCGCCCTGCGGAGCCTCTCCCCCCTCCCCCATCCTATGGCCACCAGCCACAG A C TGFB1I1 Ensembl:ENSG00000140682 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31473477..31473775 32194978 MeRIP-seq:(Medium) rs775993447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1706074,Human_Splice_Rec_1706075,Human_Splice_Rec_1706104,Human_Splice_Rec_1706106,Human_Splice_Rec_1706107,Human_Splice_Rec_1706126,Human_Splice_Rec_1706127,Human_Splice_Rec_1706144,Human_Splice_Rec_1706145,Human_Splice_Rec_1706148,Human_Splice_Rec_1706154,Human_Splice_Rec_1706155,Human_Splice_Rec_1706164,Human_Splice_Rec_1706165,Human_Splice_Rec_1706169,Human_Splice_Rec_1706180,Human_Splice_Rec_1706181,Human_Splice_Rec_1706194,Human_Splice_Rec_1706195,Human_Splice_Rec_1706213,Human_Splice_Rec_1706218,Human_Splice_Rec_1706219,Human_Splice_Rec_1706237,Human_Splice_Rec_1706255,Human_Splice_Rec_1706267 RMVar_hsa_circ_104017,RMVar_hsa_circ_100940,RMVar_hsa_circ_178044,RMVar_hsa_circ_108410,RMVar_hsa_circ_178045,RMVar_hsa_circ_325906,RMVar_hsa_circ_178046 85311 RMVar_ID_85311 Human_SNP_ID_599791341 m1A Human chr16 + 31473524 31473524 31473524 GGGCTCCCAAAGAGCGCCCTGCGGAGCCTCTCACCCCTCCCCCATCCTATGGCCACCAGCCACAG GGGCTCCCAAAGAGCGCCCTGCGGAGCCTCTCGCCCCTCCCCCATCCTATGGCCACCAGCCACAG A G TGFB1I1 Ensembl:ENSG00000140682 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31473477..31473775 32194978 MeRIP-seq:(Medium) rs775993447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1706074,Human_Splice_Rec_1706075,Human_Splice_Rec_1706104,Human_Splice_Rec_1706106,Human_Splice_Rec_1706107,Human_Splice_Rec_1706126,Human_Splice_Rec_1706127,Human_Splice_Rec_1706144,Human_Splice_Rec_1706145,Human_Splice_Rec_1706148,Human_Splice_Rec_1706154,Human_Splice_Rec_1706155,Human_Splice_Rec_1706164,Human_Splice_Rec_1706165,Human_Splice_Rec_1706169,Human_Splice_Rec_1706180,Human_Splice_Rec_1706181,Human_Splice_Rec_1706194,Human_Splice_Rec_1706195,Human_Splice_Rec_1706213,Human_Splice_Rec_1706218,Human_Splice_Rec_1706219,Human_Splice_Rec_1706237,Human_Splice_Rec_1706255,Human_Splice_Rec_1706267 RMVar_hsa_circ_104017,RMVar_hsa_circ_100940,RMVar_hsa_circ_178044,RMVar_hsa_circ_108410,RMVar_hsa_circ_178045,RMVar_hsa_circ_325906,RMVar_hsa_circ_178046 85312 RMVar_ID_85312 Human_SNP_ID_599797456 m1A Human chr16 - 31492249 31492249 31492249 ACACATGGGCTGATGCTTGGGGCCCTGCAGGGAGATGGACCCCTTCCAGCAGAGCTGGAGGAGCT ACACATGGGCTGATGCTTGGGGCCCTGCAGGGTGATGGACCCCTTCCAGCAGAGCTGGAGGAGCT T A C16orf58 Ensembl:ENSG00000140688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31492090..31492285 26863196 MeRIP-seq:(Medium) rs758198355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818773,Human_RBP_ID_18986227,Human_RBP_ID_26330041,Human_RBP_ID_26446085 Human_Splice_Rec_1706382,Human_Splice_Rec_1706383,Human_Splice_Rec_1706406,Human_Splice_Rec_1706407,Human_Splice_Rec_1706412,Human_Splice_Rec_1706413,Human_Splice_Rec_1706436,Human_Splice_Rec_1706437,Human_Splice_Rec_1706462,Human_Splice_Rec_1706463 Human_miRNA_ID_2385485 RMVar_hsa_circ_11795,RMVar_hsa_circ_299524,RMVar_hsa_circ_59505,RMVar_hsa_circ_115697,RMVar_hsa_circ_116899,RMVar_hsa_circ_178056,RMVar_hsa_circ_178057 85313 RMVar_ID_85313 Human_SNP_ID_599797749 m1A Human chr16 - 31493195 31493195 31493195 GGATACAGGAAGAAAGGATGGATTTGGTGTGTATGGGTAATGGCTGAGGGAGAGAGGAAGCGAGG GGATACAGGAAGAAAGGATGGATTTGGTGTGTGTGGGTAATGGCTGAGGGAGAGAGGAAGCGAGG T C C16orf58 Ensembl:ENSG00000140688 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:31493061..31493318 26863196 MeRIP-seq:(Medium) rs771096658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5776,Human_RBP_ID_261005,Human_RBP_ID_888705,Human_RBP_ID_3947625,Human_RBP_ID_5317550,Human_RBP_ID_5355838,Human_RBP_ID_5646853,Human_RBP_ID_8231262,Human_RBP_ID_9345636,Human_RBP_ID_17256340,Human_RBP_ID_18163238,Human_RBP_ID_18419474,Human_RBP_ID_19071496,Human_RBP_ID_22652020,Human_RBP_ID_22739374,Human_RBP_ID_23687808,Human_RBP_ID_26328971 RMVar_hsa_circ_11795,RMVar_hsa_circ_299524,RMVar_hsa_circ_59505,RMVar_hsa_circ_101404,RMVar_hsa_circ_116899,RMVar_hsa_circ_178057,RMVar_hsa_circ_178058 85314 RMVar_ID_85314 Human_SNP_ID_599797756 m1A Human chr16 - 31493213 31493212 31493213 TGGGGAAGTTGGATGACTGGATACAGGAAGAAAGGATGGATTTGGTGTGTATGGGTAATGGCTGA TGGGGAAGTTGGATGACTGGATACAGGAAGAA_GGATGGATTTGGTGTGTATGGGTAATGGCTGA CT C C16orf58 Ensembl:ENSG00000140688 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31493042..31493346 26863196 MeRIP-seq:(Medium) rs771779417 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_888705,Human_RBP_ID_3947626,Human_RBP_ID_5355838,Human_RBP_ID_8231262,Human_RBP_ID_22739374,Human_RBP_ID_23687808,Human_RBP_ID_26328971 RMVar_hsa_circ_11795,RMVar_hsa_circ_299524,RMVar_hsa_circ_59505,RMVar_hsa_circ_101404,RMVar_hsa_circ_116899,RMVar_hsa_circ_178057,RMVar_hsa_circ_178058 85315 RMVar_ID_85315 Human_SNP_ID_599797767 m1A Human chr16 + 31493237 31493237 31493237 ATCCATCCTTTCTTCCTGTATCCAGTCATCCAACTTCCCCATCTACCCATCCTTCCTTCACCCAT ATCCATCCTTTCTTCCTGTATCCAGTCATCCAGCTTCCCCATCTACCCATCCTTCCTTCACCCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31493211..31493318 26863196 MeRIP-seq:(Medium) rs1426923098 Functional Loss SNV dbSNP153 33..33 33 - - - 85316 RMVar_ID_85316 Human_SNP_ID_599797975 m1A Human chr16 + 31493725 31493725 31493725 CTTCGTTCAAGGTCTCCATGACCAGGGCTCGGACCGCGCGGTAGTTGGCGTAGATGTGGAGGGCA CTTCGTTCAAGGTCTCCATGACCAGGGCTCGGTCCGCGCGGTAGTTGGCGTAGATGTGGAGGGCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31493676..31493775 32194978 MeRIP-seq:(Medium) rs767617953 Functional Loss SNV dbSNP153 33..33 33 - - - 85317 RMVar_ID_85317 Human_SNP_ID_599801862 m1A Human chr16 - 31508349 31508349 31508349 AGCTCGGCATGGCTGACGACGCGGGTTTGGAGACCCCGCTGTGTTCCGAGCAGTTCGGCTCCGGG AGCTCGGCATGGCTGACGACGCGGGTTTGGAGGCCCCGCTGTGTTCCGAGCAGTTCGGCTCCGGG T C C16orf58 Ensembl:ENSG00000140688 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:31508201..31508400;chr16:31508197..31508400 26863196 MeRIP-seq:(Medium) rs1306701868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393804,Human_RBP_ID_18418727,Human_RBP_ID_22441497 Human_Splice_Rec_1706441 85318 RMVar_ID_85318 Human_SNP_ID_600160798 m1A Human chr16 - 32885666 32885666 32885666 GACTGCTTCTGACTGCGCCGCCTGTGACCCGCACCCCGCCGCTCTCCCGCCGCCCCGTCCCCCGG GACTGCTTCTGACTGCGCCGCCTGTGACCCGCCCCCCGCCGCTCTCCCGCCGCCCCGTCCCCCGG T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:32885575..32885668 26863410 MeRIP-seq:(Medium) rs1311777002 Functional Loss SNV dbSNP153 33..33 33 - - - 85319 RMVar_ID_85319 Human_SNP_ID_600422165 m1A Human chr16 + 34097402 34097402 34097402 CCATGCCATGCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATGCCATTCCATT CCATGCCATGCCATTCCATTCCATTCCATTCCGTTCCATTCCATTCCATTCCATGCCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:34097354..34097446 26863196 MeRIP-seq:(Medium) rs796588838 Functional Loss SNV dbSNP153 33..33 33 - - - 85320 RMVar_ID_85320 Human_SNP_ID_600458667 m1A Human chr16 + 34160735 34160735 34160735 AGCTCCTAGTTGGATCTTGGGAGCGGGCGGGCAGTCCGCCATGAGGCGAGCCACTGCCCGTCCCC AGCTCCTAGTTGGATCTTGGGAGCGGGCGGGCGGTCCGCCATGAGGCGAGCCACTGCCCGTCCCC A G RF01960-006,RF01960-006:2,RF01960-006:3,RF01960-006:4,lnc-TP53TG3F-20,lnc-TP53TG3F-20:2,RF01960-006:5,lnc-TP53TG3F-20:3,RF01960-006:6,RF01960-006:7,RF01960-006:8,RF01960-006:9,RF01960-006:10 RNACentral:URS00008CFB1A,RNACentral:URS00008C6B98,RNACentral:URS00008C8E54,RNACentral:URS00006383AF,RNACentral:URS00009C475F,RNACentral:URS00009BBBDD,RNACentral:URS00008C8AE2,RNACentral:URS00009B5DA0,RNACentral:URS00008CE4EF,RNACentral:URS00008CEF8F,RNACentral:URS00006D484A,RNACentral:URS00008CFDE8,RNACentral:URS00008CFFF7 rRNA,rRNA,rRNA,rRNA,lincRNA,lincRNA,rRNA,lincRNA,rRNA,rRNA,rRNA,rRNA,rRNA exon,exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs405629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269691,Human_RBP_ID_277498,Human_RBP_ID_482760,Human_RBP_ID_1004373,Human_RBP_ID_1088624,Human_RBP_ID_1178007,Human_RBP_ID_1281982,Human_RBP_ID_1365651,Human_RBP_ID_1517982,Human_RBP_ID_2473851,Human_RBP_ID_4400007,Human_RBP_ID_5180700,Human_RBP_ID_5274668,Human_RBP_ID_5419281,Human_RBP_ID_5440510,Human_RBP_ID_5465095,Human_RBP_ID_5495633,Human_RBP_ID_5571725,Human_RBP_ID_6511013,Human_RBP_ID_8253160,Human_RBP_ID_8433206,Human_RBP_ID_8812874,Human_RBP_ID_9062050,Human_RBP_ID_10483087,Human_RBP_ID_17063007,Human_RBP_ID_17067752,Human_RBP_ID_17188547,Human_RBP_ID_17486333,Human_RBP_ID_17690238,Human_RBP_ID_17884715,Human_RBP_ID_18178567,Human_RBP_ID_18200037,Human_RBP_ID_18207395,Human_RBP_ID_18437671,Human_RBP_ID_18512992,Human_RBP_ID_18529779,Human_RBP_ID_18678859,Human_RBP_ID_20093839,Human_RBP_ID_22388762,Human_RBP_ID_22497869,Human_RBP_ID_22801508,Human_RBP_ID_22945957,Human_RBP_ID_23128296,Human_RBP_ID_23164100,Human_RBP_ID_23274002,Human_RBP_ID_23307547,Human_RBP_ID_23688167,Human_RBP_ID_24413175,Human_RBP_ID_24477577,Human_RBP_ID_25208149,Human_RBP_ID_26441050,Human_RBP_ID_26637107,Human_RBP_ID_26748751,Human_RBP_ID_26944534,Human_RBP_ID_27156317,Human_RBP_ID_27241678,Human_RBP_ID_27442392 85321 RMVar_ID_85321 Human_SNP_ID_600458750 m1A Human chr16 + 34160865 34160865 34160865 TTTGAAAAAATTAGAGTGTTCAAAGCAGGTCCAAGCCGCCTGGATACCGCAGCTAGGAATAATGG TTTGAAAAAATTAGAGTGTTCAAAGCAGGTCCGAGCCGCCTGGATACCGCAGCTAGGAATAATGG A G RF01960-006,RF01960-006:2,RF01960-006:3,RF01960-006:4,lnc-TP53TG3F-20,lnc-TP53TG3F-20:2,RF01960-006:5,lnc-TP53TG3F-20:3,RF01960-006:6,RF01960-006:7,RF01960-006:8,RF01960-006:9,RF01960-006:10 RNACentral:URS00008CFB1A,RNACentral:URS00008C6B98,RNACentral:URS00008C8E54,RNACentral:URS00006383AF,RNACentral:URS00009C475F,RNACentral:URS00009BBBDD,RNACentral:URS00008C8AE2,RNACentral:URS00009B5DA0,RNACentral:URS00008CE4EF,RNACentral:URS00008CEF8F,RNACentral:URS00006D484A,RNACentral:URS00008CFDE8,RNACentral:URS00008CFFF7 rRNA,rRNA,rRNA,rRNA,lincRNA,lincRNA,rRNA,lincRNA,rRNA,rRNA,rRNA,rRNA,rRNA exon,exon,exon,exon,intron,exon,exon,intron,exon,exon,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62028831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269755,Human_RBP_ID_277501,Human_RBP_ID_473698,Human_RBP_ID_1004378,Human_RBP_ID_1088629,Human_RBP_ID_1130662,Human_RBP_ID_1178020,Human_RBP_ID_1238079,Human_RBP_ID_1281994,Human_RBP_ID_1365660,Human_RBP_ID_1527442,Human_RBP_ID_1842111,Human_RBP_ID_2473859,Human_RBP_ID_3494762,Human_RBP_ID_4400019,Human_RBP_ID_5184272,Human_RBP_ID_5274816,Human_RBP_ID_5419300,Human_RBP_ID_5440517,Human_RBP_ID_5466017,Human_RBP_ID_5495641,Human_RBP_ID_5571730,Human_RBP_ID_6511023,Human_RBP_ID_8088615,Human_RBP_ID_8252144,Human_RBP_ID_8433217,Human_RBP_ID_8807524,Human_RBP_ID_9062059,Human_RBP_ID_9256763,Human_RBP_ID_9284864,Human_RBP_ID_9825554,Human_RBP_ID_10483089,Human_RBP_ID_12728509,Human_RBP_ID_17002206,Human_RBP_ID_17063013,Human_RBP_ID_17067755,Human_RBP_ID_17121100,Human_RBP_ID_17188550,Human_RBP_ID_17254209,Human_RBP_ID_17369701,Human_RBP_ID_17486341,Human_RBP_ID_17690250,Human_RBP_ID_17876389,Human_RBP_ID_18178832,Human_RBP_ID_18199872,Human_RBP_ID_18207404,Human_RBP_ID_18437675,Human_RBP_ID_18529784,Human_RBP_ID_18688682,Human_RBP_ID_19031008,Human_RBP_ID_20093841,Human_RBP_ID_21888565,Human_RBP_ID_21925429,Human_RBP_ID_22201829,Human_RBP_ID_22388764,Human_RBP_ID_22421665,Human_RBP_ID_22497873,Human_RBP_ID_22802976,Human_RBP_ID_22945963,Human_RBP_ID_23128304,Human_RBP_ID_23164103,Human_RBP_ID_23274007,Human_RBP_ID_23307553,Human_RBP_ID_23688176,Human_RBP_ID_24531095,Human_RBP_ID_25208157,Human_RBP_ID_26446759,Human_RBP_ID_26637115,Human_RBP_ID_26748770,Human_RBP_ID_26944536,Human_RBP_ID_27155987,Human_RBP_ID_27241683,Human_RBP_ID_27442404,Human_RBP_ID_27560126,Human_RBP_ID_27658267 85322 RMVar_ID_85322 Human_SNP_ID_600459080 m1A Human chr16 + 34161524 34161524 34161524 GCCTTCAGCCACCCGAAATTGAGCAATAACAGATCTGTGATGCCCTTAGATGTCCGGGACTGCAC GCCTTCAGCCACCCGAAATTGAGCAATAACAGGTCTGTGATGCCCTTAGATGTCCGGGACTGCAC A G RF01960-006,lnc-TP53TG3F-19,RF01960-006:2,lnc-TP53TG3F-20,RF01960-006:3,RF01960-006:4,RF01960-006:5,RF01960-006:6,RF01960-006:7,RF01960-006:8,RF01960-006:9,RF01960-006:10 RNACentral:URS00008C8AE2,RNACentral:URS00009B9EA5,RNACentral:URS00008CFB1A,RNACentral:URS00009B5DA0,RNACentral:URS00008C6B98,RNACentral:URS00008C8E54,RNACentral:URS00006383AF,RNACentral:URS00008CE4EF,RNACentral:URS00008CEF8F,RNACentral:URS00006D484A,RNACentral:URS00008CFDE8,RNACentral:URS00008CFFF7 rRNA,lincRNA,rRNA,lincRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA exon,exon,exon,intron,exon,exon,exon,exon,exon,exon,exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62030466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269701,Human_RBP_ID_277512,Human_RBP_ID_1004386,Human_RBP_ID_1178035,Human_RBP_ID_1527451,Human_RBP_ID_1842124,Human_RBP_ID_2492259,Human_RBP_ID_3494771,Human_RBP_ID_4400042,Human_RBP_ID_5180712,Human_RBP_ID_5259265,Human_RBP_ID_5419324,Human_RBP_ID_5440539,Human_RBP_ID_5465124,Human_RBP_ID_5495665,Human_RBP_ID_5571743,Human_RBP_ID_6554819,Human_RBP_ID_8083254,Human_RBP_ID_8253165,Human_RBP_ID_8433234,Human_RBP_ID_8807541,Human_RBP_ID_9062086,Human_RBP_ID_12728537,Human_RBP_ID_17003120,Human_RBP_ID_17063027,Human_RBP_ID_17121109,Human_RBP_ID_17189300,Human_RBP_ID_17254223,Human_RBP_ID_17369710,Human_RBP_ID_17486366,Human_RBP_ID_17690268,Human_RBP_ID_17876410,Human_RBP_ID_18178576,Human_RBP_ID_18199883,Human_RBP_ID_18285486,Human_RBP_ID_18437685,Human_RBP_ID_18513003,Human_RBP_ID_18529796,Human_RBP_ID_18678883,Human_RBP_ID_20169510,Human_RBP_ID_21925438,Human_RBP_ID_22201843,Human_RBP_ID_22389127,Human_RBP_ID_22421762,Human_RBP_ID_22801538,Human_RBP_ID_23128316,Human_RBP_ID_23275023,Human_RBP_ID_23307877,Human_RBP_ID_23709882,Human_RBP_ID_24413186,Human_RBP_ID_24476269,Human_RBP_ID_24539975,Human_RBP_ID_25208170,Human_RBP_ID_26441081,Human_RBP_ID_26637125,Human_RBP_ID_26748786,Human_RBP_ID_26944550,Human_RBP_ID_27156006,Human_RBP_ID_27241705,Human_RBP_ID_27560145 85323 RMVar_ID_85323 Human_SNP_ID_718685137 m1A Human chrX - 63351181 63351181 63351181 CGTCGTCTCCTCTGCCGCCGTGCCGCAGCCGCACCAGCATCGACAACAGCTAAGTGGCCGATTCG CGTCGTCTCCTCTGCCGCCGTGCCGCAGCCGCGCCAGCATCGACAACAGCTAAGTGGCCGATTCG T C LINC01278,SPIN4 Ensembl:ENSG00000235437,Ensembl:ENSG00000186767 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:63351103..63351275 26863196 MeRIP-seq:(Medium) rs1399478110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931956,Human_RBP_ID_5069420,Human_RBP_ID_5107993,Human_RBP_ID_27150001,Human_RBP_ID_27552881 85324 RMVar_ID_85324 Human_SNP_ID_718685147 m1A Human chrX + 63351236 63351236 63351236 GGAGACGACGGGGACGAAAGGCAAGGAGTAAGAGGGATGGCTGCAGCGGCAAAGGCGCAGGCGGC GGAGACGACGGGGACGAAAGGCAAGGAGTAAGTGGGATGGCTGCAGCGGCAAAGGCGCAGGCGGC A T SPIN4-AS1 Ensembl:ENSG00000233661 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:63351185..63351303 26863196 MeRIP-seq:(Medium) rs782469806 Functional Loss SNV dbSNP153 33..33 33 - - - 85325 RMVar_ID_85325 Human_SNP_ID_718685149 m1A Human chrX + 63351248 63351248 63351248 GACGAAAGGCAAGGAGTAAGAGGGATGGCTGCAGCGGCAAAGGCGCAGGCGGCGGCAAGTCTCTG GACGAAAGGCAAGGAGTAAGAGGGATGGCTGCCGCGGCAAAGGCGCAGGCGGCGGCAAGTCTCTG A C SPIN4-AS1 Ensembl:ENSG00000233661 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:63351199..63351295 26863196 MeRIP-seq:(Medium) rs1487304676 Functional Loss SNV dbSNP153 33..33 33 - - - 85326 RMVar_ID_85326 Human_SNP_ID_718685150 m1A Human chrX + 63351248 63351248 63351248 GACGAAAGGCAAGGAGTAAGAGGGATGGCTGCAGCGGCAAAGGCGCAGGCGGCGGCAAGTCTCTG GACGAAAGGCAAGGAGTAAGAGGGATGGCTGCTGCGGCAAAGGCGCAGGCGGCGGCAAGTCTCTG A T SPIN4-AS1 Ensembl:ENSG00000233661 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:63351199..63351295 26863196 MeRIP-seq:(Medium) rs1487304676 Functional Loss SNV dbSNP153 33..33 33 - - - 85327 RMVar_ID_85327 Human_SNP_ID_718736359 m1A Human chrX + 63560899 63560899 63560899 CCACTTCGCCACGGTCTGAACTCTTGGCCACAAGATCTAAGCCTTCCGGATGCCCCAGCCAGTTC CCACTTCGCCACGGTCTGAACTCTTGGCCACACGATCTAAGCCTTCCGGATGCCCCAGCCAGTTC A C lnc-ZC3H12B-12 RNACentral:URS00008B3AEC lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:63560851..63561034 26863196 MeRIP-seq:(Medium) rs1401134335 Functional Loss SNV dbSNP153 33..33 33 - - - 85328 RMVar_ID_85328 Human_SNP_ID_718736382 m1A Human chrX + 63560989 63560989 63560989 CCTTTGCCGAGGTAGTCGGCTTACTTGATGCCAGCACACCAGGCCCCCCACCACCCGCTGGAAGC CCTTTGCCGAGGTAGTCGGCTTACTTGATGCCGGCACACCAGGCCCCCCACCACCCGCTGGAAGC A G lnc-ZC3H12B-12 RNACentral:URS00008B3AEC lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:63560785..63561017 26863196 MeRIP-seq:(Medium) rs1358111772 Functional Loss SNV dbSNP153 33..33 33 - - - 85329 RMVar_ID_85329 Human_SNP_ID_719255743 m1A Human chrX - 65518199 65518199 65518199 TAATGATGTCAAGGAAGAGGAGAAGGAGGAGAAAGAGGTCTTGCCAGACCAGGTAGAGGAGGAGG TAATGATGTCAAGGAAGAGGAGAAGGAGGAGAGAGAGGTCTTGCCAGACCAGGTAGAGGAGGAGG T C LAS1L Ensembl:ENSG00000001497 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:65518014..65518275 32194978 MeRIP-seq:(Medium) rs1325565712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1719925,Human_RBP_ID_5069573,Human_RBP_ID_8013404,Human_RBP_ID_22122827,Human_RBP_ID_23107495,Human_RBP_ID_24549929,Human_RBP_ID_26362981 RMVar_hsa_circ_91590,RMVar_hsa_circ_104698,RMVar_hsa_circ_121718,RMVar_hsa_circ_99995,RMVar_hsa_circ_66050,RMVar_hsa_circ_262745,RMVar_hsa_circ_262747,RMVar_hsa_circ_262748,RMVar_hsa_circ_262746,RMVar_hsa_circ_68469 85330 RMVar_ID_85330 Human_SNP_ID_719256181 m1A Human chrX - 65520918 65520918 65520918 CAGGAGAAAGAATAAAGCAAGTTTCAAAGTCCAGAAGGAACATGGCATGTGTATATAATGGGAGG CAGGAGAAAGAATAAAGCAAGTTTCAAAGTCCGGAAGGAACATGGCATGTGTATATAATGGGAGG T C LAS1L Ensembl:ENSG00000001497 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:65520903..65521030 26863196 MeRIP-seq:(Medium) rs780943528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_737340 RMVar_hsa_circ_91590,RMVar_hsa_circ_104698,RMVar_hsa_circ_121718,RMVar_hsa_circ_99995,RMVar_hsa_circ_66050,RMVar_hsa_circ_262745,RMVar_hsa_circ_262747,RMVar_hsa_circ_262748,RMVar_hsa_circ_262746,RMVar_hsa_circ_68469 85331 RMVar_ID_85331 Human_SNP_ID_719258696 m1A Human chrX - 65534574 65534574 65534574 CGGCCCACGGCATCGTGGTCGCCTGGCTCAGCAGGGCCGAGTGGGACCAGGTGACGGTTTATCTG CGGCCCACGGCATCGTGGTCGCCTGGCTCAGCGGGGCCGAGTGGGACCAGGTGACGGTTTATCTG T C LAS1L Ensembl:ENSG00000001497 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:65534525..65534725 32194978 MeRIP-seq:(Medium) rs984616739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5084003,Human_RBP_ID_8013446,Human_RBP_ID_18152993,Human_RBP_ID_24348820,Human_RBP_ID_26362992 Human_Splice_Rec_2213011,Human_Splice_Rec_2213035,Human_Splice_Rec_2213061,Human_Splice_Rec_2213082 RMVar_hsa_circ_104698,RMVar_hsa_circ_262748 85332 RMVar_ID_85332 Human_SNP_ID_719258714 m1A Human chrX - 65534640 65534640 65534640 GGATGGATCTCGTGTGGAGTGCGTGGTACGGAAAGTGCGTTAAAGGGAAAGGGTCGTTGCCACTC GGATGGATCTCGTGTGGAGTGCGTGGTACGGAGAGTGCGTTAAAGGGAAAGGGTCGTTGCCACTC T C LAS1L Ensembl:ENSG00000001497 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:65534601..65534775 26863196 MeRIP-seq:(Medium) rs771216409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063086,Human_RBP_ID_1716790,Human_RBP_ID_5076177,Human_RBP_ID_5330490,Human_RBP_ID_8013447,Human_RBP_ID_9316948,Human_RBP_ID_9339981,Human_RBP_ID_21997420,Human_RBP_ID_22468386,Human_RBP_ID_23103536,Human_RBP_ID_24348821,Human_RBP_ID_26362992,Human_RBP_ID_27834533 RMVar_hsa_circ_104698,RMVar_hsa_circ_262748 85333 RMVar_ID_85333 Human_SNP_ID_719258718 m1A Human chrX + 65534646 65534646 65534646 CAACGACCCTTTCCCTTTAACGCACTTTCCGTACCACGCACTCCACACGAGATCCATCCCCTGGG CAACGACCCTTTCCCTTTAACGCACTTTCCGTCCCACGCACTCCACACGAGATCCATCCCCTGGG A C lnc-ZC3H12B-2 RNACentral:URS00008B38C1 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:65534596..65534800 26863196 MeRIP-seq:(Medium) rs777149132 Functional Loss SNV dbSNP153 33..33 33 - - - 85334 RMVar_ID_85334 Human_SNP_ID_719258773 m1A Human chrX - 65534750 65534750 65534750 GAGGGTAGCACGCTGAGCTGAAGGCTGTGCGGAGCGGCGCGGCACAGAGCCTGTTGTTGAGCTCA GAGGGTAGCACGCTGAGCTGAAGGCTGTGCGGGGCGGCGCGGCACAGAGCCTGTTGTTGAGCTCA T C LAS1L Ensembl:ENSG00000001497 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:65534601..65534800 26863196 MeRIP-seq:(Medium) rs761244443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076178,Human_RBP_ID_17718593 RMVar_hsa_circ_104698,RMVar_hsa_circ_262748 85335 RMVar_ID_85335 Human_SNP_ID_719258774 m1A Human chrX - 65534750 65534750 65534750 GAGGGTAGCACGCTGAGCTGAAGGCTGTGCGGAGCGGCGCGGCACAGAGCCTGTTGTTGAGCTCA GAGGGTAGCACGCTGAGCTGAAGGCTGTGCGGCGCGGCGCGGCACAGAGCCTGTTGTTGAGCTCA T G LAS1L Ensembl:ENSG00000001497 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:65534601..65534800 26863196 MeRIP-seq:(Medium) rs761244443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076178,Human_RBP_ID_17718593 RMVar_hsa_circ_104698,RMVar_hsa_circ_262748 85336 RMVar_ID_85336 Human_SNP_ID_719285572 m1A Human chrX - 65667821 65667821 65667821 CGTTTTGGGCATGGTGGCGGCAAAGGCAGCGGAGTTGGCGAAGTTTAGCTAGGACTGTCGGGCAG CGTTTTGGGCATGGTGGCGGCAAAGGCAGCGGGGTTGGCGAAGTTTAGCTAGGACTGTCGGGCAG T C RF00017-1500 RNACentral:URS00009030E0 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:65667728..65667821 26863410 MeRIP-seq:(Medium) rs762712691 Functional Loss SNV dbSNP153 33..33 33 - - - 85337 RMVar_ID_85337 Human_SNP_ID_719285573 m1A Human chrX - 65667821 65667821 65667821 CGTTTTGGGCATGGTGGCGGCAAAGGCAGCGGAGTTGGCGAAGTTTAGCTAGGACTGTCGGGCAG CGTTTTGGGCATGGTGGCGGCAAAGGCAGCGGCGTTGGCGAAGTTTAGCTAGGACTGTCGGGCAG T G RF00017-1500 RNACentral:URS00009030E0 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:65667728..65667821 26863410 MeRIP-seq:(Medium) rs762712691 Functional Loss SNV dbSNP153 33..33 33 - - - 85338 RMVar_ID_85338 Human_SNP_ID_719297011 m1A Human chrX + 65735280 65735280 65735280 ATTGCTGATTTCCCACCAGGACTTCGTCTTCTATGCTCCCCGGCTGCGGATTAACAAGCGGATCT ATTGCTGATTTCCCACCAGGACTTCGTCTTCTGTGCTCCCCGGCTGCGGATTAACAAGCGGATCT A G MSN Ensembl:ENSG00000147065 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:65735276..65735325 26863196 MeRIP-seq:(Medium) rs746416059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94009,Human_RBP_ID_8937005,Human_RBP_ID_9339982,Human_RBP_ID_22122831,Human_RBP_ID_22468825,Human_RBP_ID_26362999,Human_RBP_ID_26835543 Human_Splice_Rec_2213143 RMVar_hsa_circ_40509,RMVar_hsa_circ_104004,RMVar_hsa_circ_128107,RMVar_hsa_circ_107842,RMVar_hsa_circ_262753,RMVar_hsa_circ_91745,RMVar_hsa_circ_262755,RMVar_hsa_circ_262756,RMVar_hsa_circ_262754,RMVar_hsa_circ_124391,RMVar_hsa_circ_113149,RMVar_hsa_circ_262762,RMVar_hsa_circ_262766,RMVar_hsa_circ_81296,RMVar_hsa_circ_262764,RMVar_hsa_circ_109605,RMVar_hsa_circ_372559,RMVar_hsa_circ_262767,RMVar_hsa_circ_116994,RMVar_hsa_circ_262765,RMVar_hsa_circ_367271,RMVar_hsa_circ_262768 85339 RMVar_ID_85339 Human_SNP_ID_719297039 m1A Human chrX + 65735427 65735427 65735427 GGCCCGGGAGGAGAAGCACCAGAAGCAGATGGAGCGGTAGGTGCTGCACACTGATGTGGGGGGCC GGCCCGGGAGGAGAAGCACCAGAAGCAGATGGGGCGGTAGGTGCTGCACACTGATGTGGGGGGCC A G MSN Ensembl:ENSG00000147065 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:65735323..65735484;chrX:65735325..65735455;chrX:65735213..65735472;chrX:65735326..65735476 26863196 MeRIP-seq:(Medium) rs150023347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24549931,Human_RBP_ID_26363001,Human_RBP_ID_27834536 Human_Splice_Rec_2213144 RMVar_hsa_circ_40509,RMVar_hsa_circ_104004,RMVar_hsa_circ_128107,RMVar_hsa_circ_107842,RMVar_hsa_circ_262753,RMVar_hsa_circ_91745,RMVar_hsa_circ_262755,RMVar_hsa_circ_262756,RMVar_hsa_circ_262754,RMVar_hsa_circ_124391,RMVar_hsa_circ_113149,RMVar_hsa_circ_262762,RMVar_hsa_circ_262766,RMVar_hsa_circ_81296,RMVar_hsa_circ_262764,RMVar_hsa_circ_109605,RMVar_hsa_circ_372559,RMVar_hsa_circ_262767,RMVar_hsa_circ_116994,RMVar_hsa_circ_262765,RMVar_hsa_circ_367271,RMVar_hsa_circ_262768 85340 RMVar_ID_85340 Human_SNP_ID_719297293 m1A Human chrX - 65736854 65736854 65736854 GCCTCTCCATCAGCTCCTCCTTCTCCCGTTCAATCTTCTCTTTCTCCTTCTCTGCCATTTCACGC GCCTCTCCATCAGCTCCTCCTTCTCCCGTTCAGTCTTCTCTTTCTCCTTCTCTGCCATTTCACGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:65736776..65736961 26863196 MeRIP-seq:(Medium) rs374474374 Functional Loss SNV dbSNP153 33..33 33 - - - 85341 RMVar_ID_85341 Human_SNP_ID_719297833 m1A Human chrX - 65739926 65739926 65739926 AGTTAGGTGTAGGAGTGTGGGGACAAGGAAAAAGGGAGGAGGGGTCCCTAGAGGCTGGGTGCCCA AGTTAGGTGTAGGAGTGTGGGGACAAGGAAAAGGGGAGGAGGGGTCCCTAGAGGCTGGGTGCCCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:65739876..65740075 26863196 MeRIP-seq:(Medium) rs1295199712 Functional Loss SNV dbSNP153 33..33 33 - - - 85342 RMVar_ID_85342 Human_SNP_ID_719298064 m1A Human chrX + 65741626 65741626 65741626 CCATGCAGTGCCCCTAGCTTAGAGCCTCCCTCAATTCCCCCTGGCCACCACCCCCCACTCTGTGC CCATGCAGTGCCCCTAGCTTAGAGCCTCCCTCGATTCCCCCTGGCCACCACCCCCCACTCTGTGC A G MSN Ensembl:ENSG00000147065 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:65741601..65741625 26863196 MeRIP-seq:(Medium) rs1196013690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94029,Human_RBP_ID_737380,Human_RBP_ID_5069761,Human_RBP_ID_17442736,Human_RBP_ID_21765765,Human_RBP_ID_24527199,Human_RBP_ID_26572568 Human_miRNA_ID_628977,Human_miRNA_ID_2946533 RMVar_hsa_circ_124391,RMVar_hsa_circ_113149,RMVar_hsa_circ_262762,RMVar_hsa_circ_262764,RMVar_hsa_circ_116994,RMVar_hsa_circ_100672,RMVar_hsa_circ_262768,RMVar_hsa_circ_262769,RMVar_hsa_circ_125185,RMVar_hsa_circ_108216,RMVar_hsa_circ_262771,RMVar_hsa_circ_109122,RMVar_hsa_circ_262772,RMVar_hsa_circ_262773 85343 RMVar_ID_85343 Human_SNP_ID_719298068 m1A Human chrX - 65741635 65741634 65741635 CAAGGTCAGGCACAGAGTGGGGGGTGGTGGCCAGGGGGAATTGAGGGAGGCTCTAAGCTAGGGGC CAAGGTCAGGCACAGAGTGGGGGGTGGTGGCC_GGGGGAATTGAGGGAGGCTCTAAGCTAGGGGC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:65741588..65741739 26863196 MeRIP-seq:(Medium) rs1204718630 Functional Loss DEL dbSNP153 33..33 33 - - - 85344 RMVar_ID_85344 Human_SNP_ID_719810983 m1A Human chrX - 67546514 67546514 67546514 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCACCCCCACCACCACCACACGGTCCATACAA CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCCCCACCACCACCACACGGTCCATACAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:67546441..67546634 26863196 MeRIP-seq:(Medium) rs866187574 Functional Loss SNV dbSNP153 33..33 33 - - - 85345 RMVar_ID_85345 Human_SNP_ID_719810984 m1A Human chrX - 67546514 67546514 67546514 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCACCCCCACCACCACCACACGGTCCATACAA CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCACCCCCACCACCACCACACGGTCCATACAA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:67546441..67546634 26863196 MeRIP-seq:(Medium) rs866187574 Functional Loss SNV dbSNP153 33..33 33 - - - 85346 RMVar_ID_85346 Human_SNP_ID_719811044 m1A Human chrX + 67546567 67546567 67546567 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGAGGCGGGAGCTGTAGCCCCCTACGGCTACACTC CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGCGGCGGGAGCTGTAGCCCCCTACGGCTACACTC A C AR Ensembl:ENSG00000169083 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chrX:67546494..67546575;chrX:67546501..67546575;chrX:67546444..67546621;chrX:67546505..67546572 26863196 MeRIP-seq:(Medium) rs1441671810 Functional Loss SNV dbSNP153 33..33 33 - - - 85347 RMVar_ID_85347 Human_SNP_ID_719811045 m1A Human chrX + 67546567 67546567 67546567 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGAGGCGGGAGCTGTAGCCCCCTACGGCTACACTC CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGCGGGAGCTGTAGCCCCCTACGGCTACACTC A G AR Ensembl:ENSG00000169083 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chrX:67546494..67546575;chrX:67546501..67546575;chrX:67546444..67546621;chrX:67546505..67546572 26863196 MeRIP-seq:(Medium) rs1441671810 Functional Loss SNV dbSNP153 33..33 33 - - - 85348 RMVar_ID_85348 Human_SNP_ID_719951137 m1A Human chrX - 68208054 68208051 68208055 GAAAGAATGAAAGAAAGAAAAGAAAAGAAAGAAAGGAAAGAAAAAGGAAAGAAAGAAAGGAAAGA GAAAGAATGAAAGAAAGAAAAGAAAAGAAAG____GAAAGAAAAAGGAAAGAAAGAAAGGAAAGA CCTTT C OPHN1 Ensembl:ENSG00000079482 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:68208003..68208078 26863196 MeRIP-seq:(Medium) rs1181148298 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_15711,RMVar_hsa_circ_337421,RMVar_hsa_circ_51524,RMVar_hsa_circ_337907,RMVar_hsa_circ_25428,RMVar_hsa_circ_16083,RMVar_hsa_circ_28822,RMVar_hsa_circ_262816,RMVar_hsa_circ_262821,RMVar_hsa_circ_17587,RMVar_hsa_circ_313949,RMVar_hsa_circ_341219,RMVar_hsa_circ_44826,RMVar_hsa_circ_9388,RMVar_hsa_circ_19364,RMVar_hsa_circ_262826,RMVar_hsa_circ_324800,RMVar_hsa_circ_28017,RMVar_hsa_circ_68401,RMVar_hsa_circ_262828,RMVar_hsa_circ_9973 85349 RMVar_ID_85349 Human_SNP_ID_719985442 m1A Human chrX - 68399156 68399156 68399156 GAACTGTATTAATGGGATATTTAGGAGTTTACATAAATCGGACTTGGTGATAAATTGGATATGGA GAACTGTATTAATGGGATATTTAGGAGTTTACGTAAATCGGACTTGGTGATAAATTGGATATGGA T C OPHN1 Ensembl:ENSG00000079482 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:68399114..68399228 26863196 MeRIP-seq:(Medium) rs920311386 Functional Loss SNV dbSNP153 33..33 33 - - - 85350 RMVar_ID_85350 Human_SNP_ID_720032992 m1A Human chrX + 68649854 68649854 68649854 ACTCCAGCAGTAGTGGGCAGGGATGGTGTGGAAGGGCCCAAGTGGAGATGCAGAGGCCAGGAAGG ACTCCAGCAGTAGTGGGCAGGGATGGTGTGGACGGGCCCAAGTGGAGATGCAGAGGCCAGGAAGG A C STARD8 Ensembl:ENSG00000130052 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:68649836..68649956 26863196 MeRIP-seq:(Medium) rs1009087613 Functional Loss SNV dbSNP153 33..33 33 - - - 85351 RMVar_ID_85351 Human_SNP_ID_720032993 m1A Human chrX - 68649870 68649870 68649870 TCCACTGCAGCTGCCTCCTTCCTGGCCTCTGCATCTCCACTTGGGCCCTTCCACACCATCCCTGC TCCACTGCAGCTGCCTCCTTCCTGGCCTCTGCCTCTCCACTTGGGCCCTTCCACACCATCCCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:68649838..68649922 26863196 MeRIP-seq:(Medium) rs1428898661 Functional Loss SNV dbSNP153 33..33 33 - - - 85352 RMVar_ID_85352 Human_SNP_ID_720069404 m1A Human chrX - 68838619 68838619 68838619 TCGGATAGATCACCAAGCCCTTCCCACTCAGGAACCTGCCCAGAAGGAAGAAGATGGTCAGCCTC TCGGATAGATCACCAAGCCCTTCCCACTCAGGGACCTGCCCAGAAGGAAGAAGATGGTCAGCCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:68829086..68840762 32194978 MeRIP-seq:(Medium) rs1556105849 Functional Loss SNV dbSNP153 33..33 33 - - - 85353 RMVar_ID_85353 Human_SNP_ID_720127208 m1A Human chrX + 69163108 69163108 69163108 GGACTTCGGAGTTCGTCTTTCTCTGGCTGGCAATCCTTTCCCGCTGGCTCGTGGGTGGCCTGAAA GGACTTCGGAGTTCGTCTTTCTCTGGCTGGCAGTCCTTTCCCGCTGGCTCGTGGGTGGCCTGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:69162878..69163176 32194978 MeRIP-seq:(Medium) rs1349064638 Functional Loss SNV dbSNP153 33..33 33 - - - 85354 RMVar_ID_85354 Human_SNP_ID_720225849 m1A Human chrX + 69702448 69702446 69702449 GAATTGTCCTGAGGAGGGGAAGGTGTAGGAAAAGAAGTGGATACTGCTGATTGGGAAGATGGTGG GAATTGTCCTGAGGAGGGGAAGGTGTAGGAA___AAGTGGATACTGCTGATTGGGAAGATGGTGG AAAG A EDA Ensembl:ENSG00000158813 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:69702412..69702560 26863196 MeRIP-seq:(Medium) rs1382869931 Functional Loss DEL dbSNP153 32..34 33 - - - 85355 RMVar_ID_85355 Human_SNP_ID_720300474 m1A Human chrX + 70137198 70137198 70137198 GAGGGTTGAATCTACAGGAAACCTGGTGATCAATTGGTTGTGGGAGGTGAGATAGAAGGAAGCAG GAGGGTTGAATCTACAGGAAACCTGGTGATCAGTTGGTTGTGGGAGGTGAGATAGAAGGAAGCAG A G IGBP1 Ensembl:ENSG00000089289 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:70137192..70137419 26863196 MeRIP-seq:(Medium) rs1475087103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77551,RMVar_hsa_circ_262844 85356 RMVar_ID_85356 Human_SNP_ID_720332129 m1A Human chrX + 70320724 70320724 70320724 GAGGGGAAGAAGAGAGAGGTTGATTAATGGGTATAAACATACAGTTAGATGGAATAAGTTCTAAT GAGGGGAAGAAGAGAGAGGTTGATTAATGGGTGTAAACATACAGTTAGATGGAATAAGTTCTAAT A G KIF4A Ensembl:ENSG00000090889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:70320676..70320760 26863196 MeRIP-seq:(Medium) rs1223887557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17844,RMVar_hsa_circ_92644,RMVar_hsa_circ_73513,RMVar_hsa_circ_114916,RMVar_hsa_circ_262849,RMVar_hsa_circ_262851 85357 RMVar_ID_85357 Human_SNP_ID_720342122 m1A Human chrX + 70374226 70374226 70374226 AGGAAAAGGAAGAATTGGTTCTTGAACTTCAGACAGCAAAGAAGGATGCCAACCAAGCCAAGTAA AGGAAAAGGAAGAATTGGTTCTTGAACTTCAGGCAGCAAAGAAGGATGCCAACCAAGCCAAGTAA A G KIF4A Ensembl:ENSG00000090889 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:70374151..70375300 32194978 MeRIP-seq:(Medium) rs375947276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93264,Human_RBP_ID_2076684,Human_RBP_ID_26363930 Human_Splice_Rec_2214267,Human_Splice_Rec_2214268 RMVar_hsa_circ_12332,RMVar_hsa_circ_107558,RMVar_hsa_circ_92644,RMVar_hsa_circ_114916,RMVar_hsa_circ_262849,RMVar_hsa_circ_262851,RMVar_hsa_circ_86188,RMVar_hsa_circ_262854,RMVar_hsa_circ_262856,RMVar_hsa_circ_342325,RMVar_hsa_circ_362772,RMVar_hsa_circ_262860,RMVar_hsa_circ_111193,RMVar_hsa_circ_274251,RMVar_hsa_circ_100960,RMVar_hsa_circ_262861,RMVar_hsa_circ_262858,RMVar_hsa_circ_262859,RMVar_hsa_circ_350541 85358 RMVar_ID_85358 Human_SNP_ID_720347372 m1A Human chrX + 70407041 70407041 70407041 TGAGGGGGATGACGAGGAATGGAAGCCAACAAAATTAGTTAAGGTGTCCAGGAAGAACATCCAAG TGAGGGGGATGACGAGGAATGGAAGCCAACAAGATTAGTTAAGGTGTCCAGGAAGAACATCCAAG A G KIF4A Ensembl:ENSG00000090889 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:70406940..70407040 32194978 MeRIP-seq:(Medium) rs1200236367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8937067 Human_Splice_Rec_2214292 RMVar_hsa_circ_100960,RMVar_hsa_circ_262861,RMVar_hsa_circ_89286,RMVar_hsa_circ_262867,RMVar_hsa_circ_262868,RMVar_hsa_circ_277862 85359 RMVar_ID_85359 Human_SNP_ID_720355337 m1A Human chrX + 70452594 70452593 70452594 TGGCGGGCAGGCAGCAGTGGAGCCGGAAGGGTAGGCAGCCAGGGGAGAGAGAGAGGAGCTATGGA TGGCGGGCAGGCAGCAGTGGAGCCGGAAGGGT_GGCAGCCAGGGGAGAGAGAGAGGAGCTATGGA TA T DLG3 Ensembl:ENSG00000082458 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:70452512..70452613 26863196 MeRIP-seq:(Medium) rs1273478062 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107206,RMVar_hsa_circ_328357,RMVar_hsa_circ_262873,RMVar_hsa_circ_85373,RMVar_hsa_circ_262872 85360 RMVar_ID_85360 Human_SNP_ID_720355418 m1A Human chrX + 70452754 70452754 70452754 CGCTCCGCTCCCTGCGGCCCGGAGGGGATGCCAGGTAGGAGTGGAGGGCTAGGAGCAAGAGCATC CGCTCCGCTCCCTGCGGCCCGGAGGGGATGCCCGGTAGGAGTGGAGGGCTAGGAGCAAGAGCATC A C DLG3 Ensembl:ENSG00000082458 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:70452718..70452820 32194978 MeRIP-seq:(Medium) rs1051718631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2214547 RMVar_hsa_circ_107206,RMVar_hsa_circ_328357,RMVar_hsa_circ_262873,RMVar_hsa_circ_85373,RMVar_hsa_circ_262872 85361 RMVar_ID_85361 Human_SNP_ID_720355419 m1A Human chrX + 70452754 70452754 70452754 CGCTCCGCTCCCTGCGGCCCGGAGGGGATGCCAGGTAGGAGTGGAGGGCTAGGAGCAAGAGCATC CGCTCCGCTCCCTGCGGCCCGGAGGGGATGCCGGGTAGGAGTGGAGGGCTAGGAGCAAGAGCATC A G DLG3 Ensembl:ENSG00000082458 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:70452718..70452820 32194978 MeRIP-seq:(Medium) rs1051718631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2214547 RMVar_hsa_circ_107206,RMVar_hsa_circ_328357,RMVar_hsa_circ_262873,RMVar_hsa_circ_85373,RMVar_hsa_circ_262872 85362 RMVar_ID_85362 Human_SNP_ID_720355834 m1A Human chrX - 70455243 70455243 70455243 GCCCCACCTCACCTGGCGCCGGGTCGGAGTCCAGATCTAGTGCTGAGAAAGCGCCAGCTCCGGCC GCCCCACCTCACCTGGCGCCGGGTCGGAGTCCTGATCTAGTGCTGAGAAAGCGCCAGCTCCGGCC T A DLG3-AS1 Ensembl:ENSG00000231651 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:70455194..70455311 26863196 MeRIP-seq:(Medium) rs1159683149 Functional Loss SNV dbSNP153 33..33 33 - - - 85363 RMVar_ID_85363 Human_SNP_ID_720361988 m1A Human chrX - 70493410 70493410 70493410 CTTTGCTCTTGTAAAATGGAAACTTTCGAGAGAGGCGGAAACTCTTTTTACGTTTCGTTTTGATC CTTTGCTCTTGTAAAATGGAAACTTTCGAGAGTGGCGGAAACTCTTTTTACGTTTCGTTTTGATC T A RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:70493404..70495437 32194978 MeRIP-seq:(Medium) rs749326117 Functional Loss SNV dbSNP153 33..33 33 - - - 85364 RMVar_ID_85364 Human_SNP_ID_720363886 m1A Human chrX + 70504157 70504157 70504157 GGCAGTACAATGGCTTGAAGGCAAAAAGGGATAAAGTGACAGCCGACTGTGACTCTGGTGAGGAG GGCAGTACAATGGCTTGAAGGCAAAAAGGGATGAAGTGACAGCCGACTGTGACTCTGGTGAGGAG A G DLG3 Ensembl:ENSG00000082458 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:70504107..70504227 26863196 MeRIP-seq:(Medium) rs771300631 Functional Loss SNV dbSNP153 33..33 33 - - - 85365 RMVar_ID_85365 Human_SNP_ID_720465320 m1A Human chrX + 71059452 71059450 71059453 CTATAACAGAGGATACAAATCAAAAAGGCAGCAACAACAACATTGGCGAGGTGGGAAAGGGAGCA CTATAACAGAGGATACAAATCAAAAAGGCAG___CAACAACATTGGCGAGGTGGGAAAGGGAGCA GCAA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:71059401..71059501 32194978 MeRIP-seq:(Medium) rs1309490376 Functional Loss DEL dbSNP153 32..34 33 - - - 85366 RMVar_ID_85366 Human_SNP_ID_720465362 m1A Human chrX - 71059749 71059749 71059749 TGGTTTGTTTGCTGGGGCCCAACGTCTGTCCCAAGTGGTGGGGTGAGAGTAAGTTAACTTTGGTG TGGTTTGTTTGCTGGGGCCCAACGTCTGTCCCGAGTGGTGGGGTGAGAGTAAGTTAACTTTGGTG T C SNX12 Ensembl:ENSG00000147164 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71059699..71059770 26863196 MeRIP-seq:(Medium) rs1257952699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_737857,Human_RBP_ID_5070625,Human_RBP_ID_24349822,Human_RBP_ID_24394133 85367 RMVar_ID_85367 Human_SNP_ID_720466812 m1A Human chrX - 71068192 71068192 71068192 ACTTCCTGGAGATCGACATCTTTAATCCTCAGACGGTGGGCGTGGGACGCGCGCGCTTCACCACC ACTTCCTGGAGATCGACATCTTTAATCCTCAGGCGGTGGGCGTGGGACGCGCGCGCTTCACCACC T C SNX12 Ensembl:ENSG00000147164 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:71068094..71068363 26863196 MeRIP-seq:(Medium) rs1316036808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_737893,Human_RBP_ID_1063150,Human_RBP_ID_5070685,Human_RBP_ID_26835570 Human_Splice_Rec_2214901,Human_Splice_Rec_2214917,Human_Splice_Rec_2214925,Human_Splice_Rec_2214931,Human_Splice_Rec_2214934,Human_Splice_Rec_2214938 RMVar_hsa_circ_90188,RMVar_hsa_circ_262884 85368 RMVar_ID_85368 Human_SNP_ID_720472012 m1A Human chrX - 71096661 71096661 71096661 CCCCAGATCTGGCTCCACCTCGGGCGGCTCGGACGGCTGGTTAGCGATCTCTGGTCGGGGAAGGG CCCCAGATCTGGCTCCACCTCGGGCGGCTCGGGCGGCTGGTTAGCGATCTCTGGTCGGGGAAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71096465..71096726 26863196 MeRIP-seq:(Medium) rs752307791 Functional Loss SNV dbSNP153 33..33 33 - - - 85369 RMVar_ID_85369 Human_SNP_ID_720473063 m1A Human chrX + 71102771 71102771 71102771 TGAAGGCTTTGTGATAGTGACATGATACAAACACTACAGACAATAAATATTAGGAGACACAGGGA TGAAGGCTTTGTGATAGTGACATGATACAAACGCTACAGACAATAAATATTAGGAGACACAGGGA A G FOXO4 Ensembl:ENSG00000184481 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71102721..71102838 26863196 MeRIP-seq:(Medium) rs1029499178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5124761,Human_RBP_ID_26573833 Human_miRNA_ID_293042 85370 RMVar_ID_85370 Human_SNP_ID_720473140 m1A Human chrX - 71103273 71103273 71103273 AACCTGATCCACATCCCCCCCCATCCCTGCTCATTTCCCAGACCCTCAGCCAAGCTCCCCAGCTC AACCTGATCCACATCCCCCCCCATCCCTGCTCGTTTCCCAGACCCTCAGCCAAGCTCCCCAGCTC T C lnc-IL2RG-4,lnc-IL2RG-4:2 RNACentral:URS00008B237F,RNACentral:URS00008B3897 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71103223..71103310 26863196 MeRIP-seq:(Medium) rs1278790370 Functional Loss SNV dbSNP153 33..33 33 - - - 85371 RMVar_ID_85371 Human_SNP_ID_720476346 m1A Human chrX + 71118665 71118665 71118665 CTTGTTGTCTCTCGGCCGCCGTCCTCTCAACCACCGCCCCCCTTTTCGGCTCCCTCTCCCCCTTC CTTGTTGTCTCTCGGCCGCCGTCCTCTCAACCGCCGCCCCCCTTTTCGGCTCCCTCTCCCCCTTC A G MED12 Ensembl:ENSG00000184634 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:71118616..71118758 26863196 MeRIP-seq:(Medium) rs1341777506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5432298,Human_RBP_ID_5455681,Human_RBP_ID_5517943,Human_RBP_ID_17442740,Human_RBP_ID_18964022 85372 RMVar_ID_85372 Human_SNP_ID_720478565 m1A Human chrX + 71129790 71129790 71129790 GCAGTGGTGGTCGGAGGCAGGGTGGCCGCAACATCTCTGTGGAGACAGCCAGTCTGGATGTCTAT GCAGTGGTGGTCGGAGGCAGGGTGGCCGCAACGTCTCTGTGGAGACAGCCAGTCTGGATGTCTAT A G MED12 Ensembl:ENSG00000184634 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71129739..71129817 26863196 MeRIP-seq:(Medium) rs1258793313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257607,Human_RBP_ID_966947,Human_RBP_ID_5411827,Human_RBP_ID_9318061,Human_RBP_ID_19026742,Human_RBP_ID_27150399 Human_Splice_Rec_2215319,Human_Splice_Rec_2215405,Human_Splice_Rec_2215489 RMVar_hsa_circ_65981,RMVar_hsa_circ_28860,RMVar_hsa_circ_262890,RMVar_hsa_circ_120769 85373 RMVar_ID_85373 Human_SNP_ID_720501873 m1A Human chrX - 71249402 71249402 71249402 AGGGCTGTGGAAGGGGGTGTGGTTCTTGGGTTATAAATAAAGGTGGCTGATGGGTCAAGGGCTGG AGGGCTGTGGAAGGGGGTGTGGTTCTTGGGTTGTAAATAAAGGTGGCTGATGGGTCAAGGGCTGG T C ZMYM3 Ensembl:ENSG00000147130 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71249351..71249437 26863196 MeRIP-seq:(Medium) rs755669920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063161,Human_RBP_ID_8015351,Human_RBP_ID_24349938 RMVar_hsa_circ_96529,RMVar_hsa_circ_262905,RMVar_hsa_circ_40799,RMVar_hsa_circ_119672,RMVar_hsa_circ_262906 85374 RMVar_ID_85374 Human_SNP_ID_720503055 m1A Human chrX + 71254536 71254536 71254536 TCACACCCTGCTCGCCCTACCTCCTGGAGCCCACTCTACCCGTGATCCCCTCCTCTCATTCAAAT TCACACCCTGCTCGCCCTACCTCCTGGAGCCCCCTCTACCCGTGATCCCCTCCTCTCATTCAAAT A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:71254467..71254686;chrX:71254485..71254669 26863196 MeRIP-seq:(Medium) rs1003841742 Functional Loss SNV dbSNP153 33..33 33 - - - 85375 RMVar_ID_85375 Human_SNP_ID_720508367 m1A Human chrX + 71283700 71283700 71283700 GGGAGAGGCCGTGTAGCGTCGCCGTTACTCCGAGGAGATACCAGTCGGTAGAGGGTGAGTTTTGG GGGAGAGGCCGTGTAGCGTCGCCGTTACTCCGGGGAGATACCAGTCGGTAGAGGGTGAGTTTTGG A G NONO Ensembl:ENSG00000147140 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:71283651..71283804;chrX:71283651..71283725;chrX:71283651..71283826 26863196 MeRIP-seq:(Medium) rs1285405963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258044,Human_RBP_ID_737955,Human_RBP_ID_800117,Human_RBP_ID_1716966,Human_RBP_ID_2076797,Human_RBP_ID_3926282,Human_RBP_ID_5070977,Human_RBP_ID_8015358,Human_RBP_ID_8937184,Human_RBP_ID_9409330,Human_RBP_ID_16919739,Human_RBP_ID_18428045,Human_RBP_ID_18454579,Human_RBP_ID_18922771,Human_RBP_ID_22630890,Human_RBP_ID_26363037 Human_Splice_Rec_2215911,Human_Splice_Rec_2215928,Human_Splice_Rec_2215951,Human_Splice_Rec_2215971,Human_Splice_Rec_2215993,Human_Splice_Rec_2216001,Human_Splice_Rec_2216009,Human_Splice_Rec_2216013,Human_Splice_Rec_2216024 85376 RMVar_ID_85376 Human_SNP_ID_720508499 m1A Human chrX + 71284338 71284338 71284338 CTTAAATTTATGGATTTCGCATCGAGTATTTTATTTTCCAGTTTGAGAAACTCTTACCATAACCT CTTAAATTTATGGATTTCGCATCGAGTATTTTCTTTTCCAGTTTGAGAAACTCTTACCATAACCT A C NONO Ensembl:ENSG00000147140 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:71284336..71284504 26863410 MeRIP-seq:(Medium) rs1238065166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2216011 85377 RMVar_ID_85377 Human_SNP_ID_720509683 m1A Human chrX + 71290720 71290720 71290720 AAAGCATCATCAACATCACCACCAGCAGCAGCACCACCAGCAGCAACAGCAGCAGCCGCCACCAC AAAGCATCATCAACATCACCACCAGCAGCAGCCCCACCAGCAGCAACAGCAGCAGCCGCCACCAC A C NONO Ensembl:ENSG00000147140 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:71290626..71292019 32194978 MeRIP-seq:(Medium) rs1163981178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257442,Human_RBP_ID_848616,Human_RBP_ID_968234,Human_RBP_ID_9409334,Human_RBP_ID_17326938,Human_RBP_ID_17442033,Human_RBP_ID_17555281,Human_RBP_ID_18922779,Human_RBP_ID_23103662,Human_RBP_ID_26363042,Human_RBP_ID_26835575,Human_RBP_ID_27150441 Human_Splice_Rec_2215932,Human_Splice_Rec_2215933,Human_Splice_Rec_2215952,Human_Splice_Rec_2215953,Human_Splice_Rec_2215974,Human_Splice_Rec_2215975,Human_Splice_Rec_2216006,Human_Splice_Rec_2216007,Human_Splice_Rec_2216015,Human_Splice_Rec_2216016,Human_Splice_Rec_2216027,Human_Splice_Rec_2216028,Human_Splice_Rec_2216035,Human_Splice_Rec_2216036,Human_Splice_Rec_2216041,Human_Splice_Rec_2216042 Human_miRNA_ID_2053155 RMVar_hsa_circ_40206,RMVar_hsa_circ_8582,RMVar_hsa_circ_43043,RMVar_hsa_circ_118976,RMVar_hsa_circ_318066,RMVar_hsa_circ_262912 85378 RMVar_ID_85378 Human_SNP_ID_720510947 m1A Human chrX + 71297002 71297002 71297002 TCAAGGAGGCTCGTGAGAAGCTGGAGATGGAGATGGAAGCTGCACGCCATGAGCACCAGGTCATG TCAAGGAGGCTCGTGAGAAGCTGGAGATGGAGGTGGAAGCTGCACGCCATGAGCACCAGGTCATG A G NONO Ensembl:ENSG00000147140 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:71296951..71297096 26863196 MeRIP-seq:(Medium) rs1370808843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257444,Human_RBP_ID_799641,Human_RBP_ID_848620,Human_RBP_ID_968242,Human_RBP_ID_1716993,Human_RBP_ID_2076840,Human_RBP_ID_3261896,Human_RBP_ID_5071021,Human_RBP_ID_8015491,Human_RBP_ID_8277041,Human_RBP_ID_9409345,Human_RBP_ID_16920212,Human_RBP_ID_17555286,Human_RBP_ID_18156212,Human_RBP_ID_19027502,Human_RBP_ID_22519747,Human_RBP_ID_22841902,Human_RBP_ID_23103692,Human_RBP_ID_24549938,Human_RBP_ID_26363049,Human_RBP_ID_27833956 Human_Splice_Rec_2215919,Human_Splice_Rec_2215941,Human_Splice_Rec_2215961,Human_Splice_Rec_2215983,Human_Splice_Rec_2216022,Human_Splice_Rec_2216051,Human_Splice_Rec_2216060,Human_Splice_Rec_2216067,Human_Splice_Rec_2216076 Human_miRNA_ID_2014393,Human_miRNA_ID_2760794 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_348374,RMVar_hsa_circ_108414,RMVar_hsa_circ_117808,RMVar_hsa_circ_262915,RMVar_hsa_circ_262917,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_262916 85379 RMVar_ID_85379 Human_SNP_ID_720510949 m1A Human chrX + 71297007 71297007 71297007 GAGGCTCGTGAGAAGCTGGAGATGGAGATGGAAGCTGCACGCCATGAGCACCAGGTCATGCTAAT GAGGCTCGTGAGAAGCTGGAGATGGAGATGGAGGCTGCACGCCATGAGCACCAGGTCATGCTAAT A G NONO Ensembl:ENSG00000147140 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71296957..71297085 26863196 MeRIP-seq:(Medium) rs750904419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257444,Human_RBP_ID_288125,Human_RBP_ID_799641,Human_RBP_ID_848620,Human_RBP_ID_968242,Human_RBP_ID_1063168,Human_RBP_ID_1716993,Human_RBP_ID_2076840,Human_RBP_ID_3261896,Human_RBP_ID_5084256,Human_RBP_ID_8015491,Human_RBP_ID_8277041,Human_RBP_ID_9409346,Human_RBP_ID_16920212,Human_RBP_ID_17555286,Human_RBP_ID_18156212,Human_RBP_ID_19027502,Human_RBP_ID_22519747,Human_RBP_ID_22841902,Human_RBP_ID_23103692,Human_RBP_ID_24549938,Human_RBP_ID_26363049,Human_RBP_ID_27833957 Human_Splice_Rec_2215919,Human_Splice_Rec_2215941,Human_Splice_Rec_2215961,Human_Splice_Rec_2215983,Human_Splice_Rec_2216022,Human_Splice_Rec_2216051,Human_Splice_Rec_2216060,Human_Splice_Rec_2216067,Human_Splice_Rec_2216076 Human_miRNA_ID_2014393,Human_miRNA_ID_2760794 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_348374,RMVar_hsa_circ_108414,RMVar_hsa_circ_117808,RMVar_hsa_circ_262915,RMVar_hsa_circ_262917,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_262916 85380 RMVar_ID_85380 Human_SNP_ID_720510962 m1A Human chrX + 71297045 71297045 71297045 ACGCCATGAGCACCAGGTCATGCTAATGAGACAGGGTGAGTCTAGGCCTGTAAGTCTTAAAGCTG ACGCCATGAGCACCAGGTCATGCTAATGAGACGGGGTGAGTCTAGGCCTGTAAGTCTTAAAGCTG A G NONO Ensembl:ENSG00000147140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:71296816..71297093;chrX:71296952..71297076 26863196 MeRIP-seq:(Medium) rs752423735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_737980,Human_RBP_ID_9409987,Human_RBP_ID_23107651,Human_RBP_ID_24549938,Human_RBP_ID_26363050,Human_RBP_ID_27833958 Human_Splice_Rec_2215919,Human_Splice_Rec_2215941,Human_Splice_Rec_2215961,Human_Splice_Rec_2215983,Human_Splice_Rec_2216022,Human_Splice_Rec_2216051,Human_Splice_Rec_2216060,Human_Splice_Rec_2216067,Human_Splice_Rec_2216076 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_348374,RMVar_hsa_circ_108414,RMVar_hsa_circ_117808,RMVar_hsa_circ_262915,RMVar_hsa_circ_262917,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_262916 85381 RMVar_ID_85381 Human_SNP_ID_720511263 m1A Human chrX + 71298667 71298667 71298667 AATTGTTTCCTTTGGCATAGAAAGAGACTAACAATCTTTATCCCTTGTGCTGATCACACTACTCT AATTGTTTCCTTTGGCATAGAAAGAGACTAACGATCTTTATCCCTTGTGCTGATCACACTACTCT A G NONO Ensembl:ENSG00000147140 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71298665..71298783 26863196 MeRIP-seq:(Medium) rs1251978389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_737994,Human_RBP_ID_967409,Human_RBP_ID_1717022,Human_RBP_ID_2076860,Human_RBP_ID_3261916,Human_RBP_ID_16920266,Human_RBP_ID_18153474,Human_RBP_ID_18406544,Human_RBP_ID_22630894,Human_RBP_ID_22692577,Human_RBP_ID_26287690,Human_RBP_ID_27794692 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_117808,RMVar_hsa_circ_262915,RMVar_hsa_circ_262917,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_262919,RMVar_hsa_circ_125016 85382 RMVar_ID_85382 Human_SNP_ID_720511271 m1A Human chrX - 71298703 71298703 71298703 GGCACCTCTGTTGTTTATGCCCATAGCACCTAAGGCAGAGTAGTGTGATCAGCACAAGGGATAAA GGCACCTCTGTTGTTTATGCCCATAGCACCTACGGCAGAGTAGTGTGATCAGCACAAGGGATAAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:71298701..71298725 26863196 MeRIP-seq:(Medium) rs746334582 Functional Loss SNV dbSNP153 33..33 33 - - - 85383 RMVar_ID_85383 Human_SNP_ID_720511543 m1A Human chrX - 71300034 71300034 71300034 CGACGTTTGTTTGGGGCAAATTCAGCTCCAGGAGCTGCACGGTTGAATGCAGGAGGAGTTCCACC CGACGTTTGTTTGGGGCAAATTCAGCTCCAGGGGCTGCACGGTTGAATGCAGGAGGAGTTCCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71299985..71300143 26863196 MeRIP-seq:(Medium) rs1172043557 Functional Loss SNV dbSNP153 33..33 33 - - - 85384 RMVar_ID_85384 Human_SNP_ID_720511576 m1A Human chrX + 71300231 71300231 71300231 TACTCTAGGGAGTATGCTGGAGGCAGAGGGCAAGGGAGGGGTGGTATTAAACAAGTCAATTCTGT TACTCTAGGGAGTATGCTGGAGGCAGAGGGCAGGGGAGGGGTGGTATTAAACAAGTCAATTCTGT A G NONO Ensembl:ENSG00000147140 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:71300119..71300725 32194978 MeRIP-seq:(Medium) rs757365853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257450,Human_RBP_ID_738015,Human_RBP_ID_799645,Human_RBP_ID_1231265,Human_RBP_ID_2076871,Human_RBP_ID_3261933,Human_RBP_ID_3926335,Human_RBP_ID_8015568,Human_RBP_ID_8226772,Human_RBP_ID_8721464,Human_RBP_ID_16920356,Human_RBP_ID_18153489,Human_RBP_ID_18173987,Human_RBP_ID_18406560,Human_RBP_ID_18922852,Human_RBP_ID_22468837,Human_RBP_ID_22630895,Human_RBP_ID_22841930,Human_RBP_ID_26572778 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_262915,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_109623,RMVar_hsa_circ_262920 85385 RMVar_ID_85385 Human_SNP_ID_720511662 m1A Human chrX + 71300558 71300558 71300558 AGGTTGATCTTGAACTCCTGACCTCGTGATCTACCCACCTCGGCCTCCCAAAATGCTGGGATTAC AGGTTGATCTTGAACTCCTGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAATGCTGGGATTAC A G NONO Ensembl:ENSG00000147140 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:71300457..71300753 26863196 MeRIP-seq:(Medium) rs1422911397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_738028,Human_RBP_ID_2076875,Human_RBP_ID_16920377,Human_RBP_ID_18964035,Human_RBP_ID_27553082 Human_Splice_Rec_2216012 Human_miRNA_ID_1167499 RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_262915,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_109623,RMVar_hsa_circ_262920 85386 RMVar_ID_85386 Human_SNP_ID_720511672 m1A Human chrX - 71300620 71300620 71300620 TCTGGGGCTGGGGGAGTGTAAGGATAAGAAGCAAGTGAGGTTGGGCACGGTGGCTCACCCCTGTA TCTGGGGCTGGGGGAGTGTAAGGATAAGAAGCGAGTGAGGTTGGGCACGGTGGCTCACCCCTGTA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:71300426..71300752 26863410 MeRIP-seq:(Medium) rs904757904 Functional Loss SNV dbSNP153 33..33 33 - - - 85387 RMVar_ID_85387 Human_SNP_ID_720514648 m1A Human chrX - 71315138 71315137 71315138 CCTCCAAAGAAGAAAGAAAAAAAGAAAAAAAAAGAAAGCTCCTGAACCAGAAGAAATTGAGGAAG CCTCCAAAGAAGAAAGAAAAAAAGAAAAAAAA_GAAAGCTCCTGAACCAGAAGAAATTGAGGAAG CT C AL590762.3 Ensembl:ENSG00000224208 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71315051..71315141 26863196 MeRIP-seq:(Medium) rs1223723180 Functional Loss DEL dbSNP153 33..33 33 - - - 85388 RMVar_ID_85388 Human_SNP_ID_720524261 m1A Human chrX + 71366419 71366419 71366419 GACAGCGACGAAGATTCCGCTGGAGGCGGCCCATTTTCTTTAGCGGGTTTCCTTTTCGGCAACAT GACAGCGACGAAGATTCCGCTGGAGGCGGCCCGTTTTCTTTAGCGGGTTTCCTTTTCGGCAACAT A G TAF1 Ensembl:ENSG00000147133 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:71366370..71366479 26863196 MeRIP-seq:(Medium) rs1477984258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18427861,Human_RBP_ID_22349081 Human_Splice_Rec_2216138,Human_Splice_Rec_2216214,Human_Splice_Rec_2216288 85389 RMVar_ID_85389 Human_SNP_ID_720542882 m1A Human chrX + 71461416 71461416 71461416 AGTCATCAGTTTAAGGAAAAGGAAGTAACATCAAATTTGTATAACTTAGGACAATGTGGGACACA AGTCATCAGTTTAAGGAAAAGGAAGTAACATCGAATTTGTATAACTTAGGACAATGTGGGACACA A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71461406..71461617 26863196 MeRIP-seq:(Medium) rs1437031804 Functional Loss SNV dbSNP153 33..33 33 - - - 85390 RMVar_ID_85390 Human_SNP_ID_720543287 m1A Human chrX + 71463937 71463937 71463937 AGAGGAGGAAGAAGATGAGGAGGAGGAAGAGCAGCGCTCTGGGCCGAGCGTACTAAGCCAGGTCC AGAGGAGGAAGAAGATGAGGAGGAGGAAGAGCGGCGCTCTGGGCCGAGCGTACTAAGCCAGGTCC A G TAF1 Ensembl:ENSG00000147133 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71463886..71463995 26863196 MeRIP-seq:(Medium) rs772126195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257441,Human_RBP_ID_8016027,Human_RBP_ID_23107345,Human_RBP_ID_24549952,Human_RBP_ID_26363107 RMVar_hsa_circ_119158,RMVar_hsa_circ_262944 85391 RMVar_ID_85391 Human_SNP_ID_720543288 m1A Human chrX + 71463937 71463937 71463937 AGAGGAGGAAGAAGATGAGGAGGAGGAAGAGCAGCGCTCTGGGCCGAGCGTACTAAGCCAGGTCC AGAGGAGGAAGAAGATGAGGAGGAGGAAGAGCTGCGCTCTGGGCCGAGCGTACTAAGCCAGGTCC A T TAF1 Ensembl:ENSG00000147133 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:71463886..71463995 26863196 MeRIP-seq:(Medium) rs772126195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257441,Human_RBP_ID_8016027,Human_RBP_ID_23107345,Human_RBP_ID_24549952,Human_RBP_ID_26363107 RMVar_hsa_circ_119158,RMVar_hsa_circ_262944 85392 RMVar_ID_85392 Human_SNP_ID_720555480 m1A Human chrX - 71533197 71533197 71533197 TTTGGAGGTAGTAGTACAAGGGCAGCAGCCGTAGCAATGCTCTGGAGGGCTTGAGCGGCGGCAGC TTTGGAGGTAGTAGTACAAGGGCAGCAGCCGTGGCAATGCTCTGGAGGGCTTGAGCGGCGGCAGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:71533096..71533230 26863410 MeRIP-seq:(Medium) rs1359623398 Functional Loss SNV dbSNP153 33..33 33 - - - 85393 RMVar_ID_85393 Human_SNP_ID_720563243 m1A Human chrX - 71579051 71579051 71579051 CACCAGCGCTCCCACTTCCCCCAAGGCCGCCAATGGTGCCCCTACTTCTCCCCACACCGTCACTG CACCAGCGCTCCCACTTCCCCCAAGGCCGCCAGTGGTGCCCCTACTTCTCCCCACACCGTCACTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71579001..71579125 26863196 MeRIP-seq:(Medium) rs1443369854 Functional Loss SNV dbSNP153 33..33 33 - - - 85394 RMVar_ID_85394 Human_SNP_ID_720563244 m1A Human chrX - 71579051 71579051 71579051 CACCAGCGCTCCCACTTCCCCCAAGGCCGCCAATGGTGCCCCTACTTCTCCCCACACCGTCACTG CACCAGCGCTCCCACTTCCCCCAAGGCCGCCACTGGTGCCCCTACTTCTCCCCACACCGTCACTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71579001..71579125 26863196 MeRIP-seq:(Medium) rs1443369854 Functional Loss SNV dbSNP153 33..33 33 - - - 85395 RMVar_ID_85395 Human_SNP_ID_720646389 m1A Human chrX + 72130953 72130953 72130953 GTGACCGAGATGGCCCAGTCCTTGGCTTCGCCAGTGAAAAAGGAGATCAGAAAGGCCACCCGCTC GTGACCGAGATGGCCCAGTCCTTGGCTTCGCCGGTGAAAAAGGAGATCAGAAAGGCCACCCGCTC A G NHSL2 Ensembl:ENSG00000204131 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:72130904..72131018 32194978 MeRIP-seq:(Medium) rs1399249573 Functional Loss SNV dbSNP153 33..33 33 - - - 85396 RMVar_ID_85396 Human_SNP_ID_720657083 m1A Human chrX + 72183712 72183712 72183712 AAGCATGGAAATGGGATGGTAGATAGAGAAGGACAGAGGATTAAGAGAAAGTTTTATTTTCTTTG AAGCATGGAAATGGGATGGTAGATAGAGAAGGGCAGAGGATTAAGAGAAAGTTTTATTTTCTTTG A G PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:72183706..72183968 26863196 MeRIP-seq:(Medium) rs1280116383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8016896,Human_RBP_ID_16924535 85397 RMVar_ID_85397 Human_SNP_ID_720657128 m1A Human chrX - 72184117 72184117 72184117 TAACTGCCTAACAAAACCTCAACCATGGCTTAAGGCTGCACCTAGCTCTTTTCAATCCTATATTG TAACTGCCTAACAAAACCTCAACCATGGCTTAGGGCTGCACCTAGCTCTTTTCAATCCTATATTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:72184110..72184613 26863196 MeRIP-seq:(Medium) rs996442545 Functional Loss SNV dbSNP153 33..33 33 - - - 85398 RMVar_ID_85398 Human_SNP_ID_720657607 m1A Human chrX + 72186465 72186465 72186465 ATGAGTACCTGTCATCTCTTCTCTAAAGGGGGAGCAGCCTCTGGGAGTGACAGTGCTGACAAGAA ATGAGTACCTGTCATCTCTTCTCTAAAGGGGGGGCAGCCTCTGGGAGTGACAGTGCTGACAAGAA A G PIN4 Ensembl:ENSG00000102309 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chrX:72186451..72196943;chrX:72186451..72186550;chrX:72186451..72186525 26863196,32194978 MeRIP-seq:(Medium) rs771318018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5155322,Human_RBP_ID_8016904,Human_RBP_ID_9341914,Human_RBP_ID_22467692,Human_RBP_ID_26363112 Human_Splice_Rec_2216933,Human_Splice_Rec_2216936,Human_Splice_Rec_2216937,Human_Splice_Rec_2216940,Human_Splice_Rec_2216941,Human_Splice_Rec_2216946,Human_Splice_Rec_2216947,Human_Splice_Rec_2216952,Human_Splice_Rec_2216953,Human_Splice_Rec_2216958,Human_Splice_Rec_2216959,Human_Splice_Rec_2216964,Human_Splice_Rec_2216965,Human_Splice_Rec_2216970,Human_Splice_Rec_2216971,Human_Splice_Rec_2216980,Human_Splice_Rec_2216981 RMVar_hsa_circ_70826 85399 RMVar_ID_85399 Human_SNP_ID_720657625 m1A Human chrX + 72186533 72186533 72186533 TCAAGGTCCCAAAGGTGGTGGCAATGCAGTAAAGGTGAGTTACTGGTTCCTTTTTTTCCATGTTA TCAAGGTCCCAAAGGTGGTGGCAATGCAGTAACGGTGAGTTACTGGTTCCTTTTTTTCCATGTTA A C PIN4 Ensembl:ENSG00000102309 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:72186501..72186550 32194978 MeRIP-seq:(Medium) rs956775117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5155322 Human_Splice_Rec_2216933,Human_Splice_Rec_2216936,Human_Splice_Rec_2216937,Human_Splice_Rec_2216940,Human_Splice_Rec_2216941,Human_Splice_Rec_2216946,Human_Splice_Rec_2216947,Human_Splice_Rec_2216952,Human_Splice_Rec_2216953,Human_Splice_Rec_2216958,Human_Splice_Rec_2216959,Human_Splice_Rec_2216964,Human_Splice_Rec_2216965,Human_Splice_Rec_2216970,Human_Splice_Rec_2216971,Human_Splice_Rec_2216980,Human_Splice_Rec_2216981 RMVar_hsa_circ_70826 85400 RMVar_ID_85400 Human_SNP_ID_720659565 m1A Human chrX - 72196889 72196889 72196889 TAATAAGAGCAACATACCCCTTGCCTGGCTTTATCTTCACTATACTGTGCGGCCACTTCATTGAA TAATAAGAGCAACATACCCCTTGCCTGGCTTTCTCTTCACTATACTGTGCGGCCACTTCATTGAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:72196776..72196925 26863196 MeRIP-seq:(Medium) rs1327836879 Functional Loss SNV dbSNP153 33..33 33 - - - 85401 RMVar_ID_85401 Human_SNP_ID_720672036 m1A Human chrX + 72272660 72272660 72272660 TTAATTACGTACAAAGATCTGACATGTCACCCAGGGACCCATTTCACCCACTGCTCTGTTTGGCC TTAATTACGTACAAAGATCTGACATGTCACCCGGGGACCCATTTCACCCACTGCTCTGTTTGGCC A G PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:72272601..72272675 26863196 MeRIP-seq:(Medium) rs373139828 Functional Loss SNV dbSNP153 33..33 33 - - - 85402 RMVar_ID_85402 Human_SNP_ID_720672331 m1A Human chrX + 72274067 72274063 72274067 AGGAACCATGGGTTCCCTAACTGCTGCAGATTAATTGTGACGCTGATCGTTCTTTCCACCCTCAA AGGAACCATGGGTTCCCTAACTGCTGCAG____ATTGTGACGCTGATCGTTCTTTCCACCCTCAA GATTA G PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:72274065..72274233 26863196 MeRIP-seq:(Medium) rs756971490 Functional Loss DEL dbSNP153 30..33 33 - - - 85403 RMVar_ID_85403 Human_SNP_ID_720672967 m1A Human chrX - 72277124 72277124 72277124 CGCCTCCATCCTCCCCCGGCCGGGGCTGCCCGAGGTTTCGGGATTCCTACTGGGGATGGCCGGGC CGCCTCCATCCTCCCCCGGCCGGGGCTGCCCGTGGTTTCGGGATTCCTACTGGGGATGGCCGGGC T A RPS4X Ensembl:ENSG00000198034 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:72277123..72277250 26863410 MeRIP-seq:(Medium) rs1340329321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5517969,Human_RBP_ID_26797179 RMVar_hsa_circ_90232,RMVar_hsa_circ_105212,RMVar_hsa_circ_262976,RMVar_hsa_circ_262986 85404 RMVar_ID_85404 Human_SNP_ID_720683688 m1A Human chrX - 72337804 72337804 72337804 AGCAAGGAGGGTGGTGGTAGGAGACAGGAGGCAAGGGACCGGCCCCTGCAGGTGAGTAACTTAGA AGCAAGGAGGGTGGTGGTAGGAGACAGGAGGCCAGGGACCGGCCCCTGCAGGTGAGTAACTTAGA T G HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:72337787..72338036 26863196 MeRIP-seq:(Medium) rs1418908981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124992,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262991 85405 RMVar_ID_85405 Human_SNP_ID_720683696 m1A Human chrX - 72337840 72337840 72337840 TTTCTGTGCTCAAGCCACACAAAGAAGACTCAAGTGAGCAAGGAGGGTGGTGGTAGGAGACAGGA TTTCTGTGCTCAAGCCACACAAAGAAGACTCATGTGAGCAAGGAGGGTGGTGGTAGGAGACAGGA T A HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:72337792..72338017;chrX:72337796..72337963 26863196 MeRIP-seq:(Medium) rs1484024017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124992,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262991 85406 RMVar_ID_85406 Human_SNP_ID_720683753 m1A Human chrX - 72338136 72338136 72338136 GAGGAAGCCAACAGCGAGCAAATAAAGAAACAAACACACAAGATGTTTTCTGTGCGCTAAGTGGA GAGGAAGCCAACAGCGAGCAAATAAAGAAACAGACACACAAGATGTTTTCTGTGCGCTAAGTGGA T C HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:72338085..72338168 26863196 MeRIP-seq:(Medium) rs1249620078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124992,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262991 85407 RMVar_ID_85407 Human_SNP_ID_720719933 m1A Human chrX - 72568883 72568883 72568883 GACCTCTCTTTGTTCTCTCTGTTATTATTAGGATAGTTAAGCCTAAAGTGGCCTCCATGGAGGAG GACCTCTCTTTGTTCTCTCTGTTATTATTAGGGTAGTTAAGCCTAAAGTGGCCTCCATGGAGGAG T C HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:72568845..72568931 26863196 MeRIP-seq:(Medium) rs782012930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16929284 Human_Splice_Rec_2217072,Human_Splice_Rec_2217092,Human_Splice_Rec_2217113,Human_Splice_Rec_2217132,Human_Splice_Rec_2217161,Human_Splice_Rec_2217182,Human_Splice_Rec_2217202,Human_Splice_Rec_2217222,Human_Splice_Rec_2217250,Human_Splice_Rec_2217271,Human_Splice_Rec_2217322,Human_Splice_Rec_2217358,Human_Splice_Rec_2217402,Human_Splice_Rec_2217423,Human_Splice_Rec_2217440,Human_Splice_Rec_2217461,Human_Splice_Rec_2217494,Human_Splice_Rec_2217512,Human_Splice_Rec_2217528,Human_Splice_Rec_2217543,Human_Splice_Rec_2217554,Human_Splice_Rec_2217583,Human_Splice_Rec_2217611,Human_Splice_Rec_2217627,Human_Splice_Rec_2217643,Human_Splice_Rec_2217658,Human_Splice_Rec_2217674,Human_Splice_Rec_2217699,Human_Splice_Rec_2217711,Human_Splice_Rec_2217729,Human_Splice_Rec_2217764,Human_Splice_Rec_2217786,Human_Splice_Rec_2217798,Human_Splice_Rec_2217811,Human_Splice_Rec_2217846,Human_Splice_Rec_2217858,Human_Splice_Rec_2217866,Human_Splice_Rec_2217874,Human_Splice_Rec_2217881,Human_Splice_Rec_2217887 RMVar_hsa_circ_78337,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262999,RMVar_hsa_circ_266524,RMVar_hsa_circ_276136 85408 RMVar_ID_85408 Human_SNP_ID_720720679 m1A Human chrX + 72572784 72572784 72572784 GCTCCTCCATCTTCCGCTTAAAACCGTTCCGCAGCCACCTTCCAGATCTGGCTTTTTTCGGACTC GCTCCTCCATCTTCCGCTTAAAACCGTTCCGCGGCCACCTTCCAGATCTGGCTTTTTTCGGACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:72572651..72572851 26863196 MeRIP-seq:(Medium) rs782180811 Functional Loss SNV dbSNP153 33..33 33 - - - 85409 RMVar_ID_85409 Human_SNP_ID_720899150 m1A Human chrX + 73563356 73563356 73563356 ATCTCGGAACTGGAGGAGGAGGAGGAAGAAGAAGCGGCAACGTCGTCGTCGTCGCCGTCGTCGTC ATCTCGGAACTGGAGGAGGAGGAGGAAGAAGAGGCGGCAACGTCGTCGTCGTCGCCGTCGTCGTC A G CHIC1 Ensembl:ENSG00000204116 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:73563212..73563765;chrX:73563249..73563520 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_24351326 85410 RMVar_ID_85410 Human_SNP_ID_720899154 m1A Human chrX - 73563366 73563363 73563366 TACCGACGACGACGACGACGGCGACGACGACGACGTTGCCGCTTCTTCTTCCTCCTCCTCCTCCA TACCGACGACGACGACGACGGCGACGACGACG___TTGCCGCTTCTTCTTCCTCCTCCTCCTCCA ACGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:73563317..73563549 26863196 MeRIP-seq:(Medium) rs771438204 Functional Loss DEL dbSNP153 33..35 33 - - - 85411 RMVar_ID_85411 Human_SNP_ID_720899205 m1A Human chrX + 73563427 73563427 73563427 GGTATCTGGGCCCGACGATGACGAGGAGGATGAGGAGGAAGAGGAGGAAGAGGAGGAGGAGGAAG GGTATCTGGGCCCGACGATGACGAGGAGGATGGGGAGGAAGAGGAGGAAGAGGAGGAGGAGGAAG A G CHIC1 Ensembl:ENSG00000204116 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:73563319..73563428 32194978 MeRIP-seq:(Medium) rs1470944285 Functional Loss SNV dbSNP153 33..33 33 - - - 85412 RMVar_ID_85412 Human_SNP_ID_720952323 m1A Human chrX - 73827728 73827728 73827728 ACGCTTTATTTCATGTCTCCTTTTTGGGTCACATGCTGTGTGCTTTTTGTCCTTTTCTTGTTCTG ACGCTTTATTTCATGTCTCCTTTTTGGGTCACGTGCTGTGTGCTTTTTGTCCTTTTCTTGTTCTG T C XIST Ensembl:ENSG00000229807 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:73827384..73827878 26863410 MeRIP-seq:(Medium) rs1490435593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287983,Human_RBP_ID_738687,Human_RBP_ID_1064182,Human_RBP_ID_1231594,Human_RBP_ID_1343108,Human_RBP_ID_1406864,Human_RBP_ID_1717874,Human_RBP_ID_2077436,Human_RBP_ID_3927295,Human_RBP_ID_5252266,Human_RBP_ID_5272442,Human_RBP_ID_8019216,Human_RBP_ID_8722315,Human_RBP_ID_10469998,Human_RBP_ID_16931178,Human_RBP_ID_17066196,Human_RBP_ID_17178823,Human_RBP_ID_17327113,Human_RBP_ID_18454688,Human_RBP_ID_18923773,Human_RBP_ID_21859410,Human_RBP_ID_22519923,Human_RBP_ID_22842387,Human_RBP_ID_23104524,Human_RBP_ID_24351635,Human_RBP_ID_24445272,Human_RBP_ID_24527511,Human_RBP_ID_26290222,Human_RBP_ID_26745415,Human_RBP_ID_27150960 Human_miRNA_ID_3036333,Human_miRNA_ID_3211223 RMVar_hsa_circ_126677,RMVar_hsa_circ_48078,RMVar_hsa_circ_263006,RMVar_hsa_circ_337157,RMVar_hsa_circ_362289,RMVar_hsa_circ_317774,RMVar_hsa_circ_263010,RMVar_hsa_circ_263011,RMVar_hsa_circ_263009 85413 RMVar_ID_85413 Human_SNP_ID_720954964 m1A Human chrX - 73842745 73842745 73842745 TGACCAGACAAGGCCCTTTCTCTTGGACTTAAACAATTCTCAGTTGCACTTTCCTTGGTCCCACC TGACCAGACAAGGCCCTTTCTCTTGGACTTAAGCAATTCTCAGTTGCACTTTCCTTGGTCCCACC T C XIST Ensembl:ENSG00000229807 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:73842582..73843055 26863196 MeRIP-seq:(Medium) rs770654670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_738805,Human_RBP_ID_1231838,Human_RBP_ID_1343236,Human_RBP_ID_1406381,Human_RBP_ID_1718254,Human_RBP_ID_2077561,Human_RBP_ID_3927498,Human_RBP_ID_5072547,Human_RBP_ID_5230947,Human_RBP_ID_5311065,Human_RBP_ID_5517990,Human_RBP_ID_5536178,Human_RBP_ID_5659646,Human_RBP_ID_8020039,Human_RBP_ID_8227573,Human_RBP_ID_8722542,Human_RBP_ID_10470560,Human_RBP_ID_16931864,Human_RBP_ID_17066207,Human_RBP_ID_17095901,Human_RBP_ID_17178857,Human_RBP_ID_17203586,Human_RBP_ID_17327150,Human_RBP_ID_17442205,Human_RBP_ID_17555463,Human_RBP_ID_18157090,Human_RBP_ID_18407070,Human_RBP_ID_18924210,Human_RBP_ID_21859983,Human_RBP_ID_22842723,Human_RBP_ID_23105117,Human_RBP_ID_23204038,Human_RBP_ID_26290960,Human_RBP_ID_26572957,Human_RBP_ID_26745586,Human_RBP_ID_27151136,Human_RBP_ID_27384186,Human_RBP_ID_27795360 Human_miRNA_ID_3146677,Human_miRNA_ID_3151120,Human_miRNA_ID_3151397,Human_miRNA_ID_3156848,Human_miRNA_ID_3161647,Human_miRNA_ID_3161882,Human_miRNA_ID_3163756,Human_miRNA_ID_3167859,Human_miRNA_ID_3167981,Human_miRNA_ID_3179233,Human_miRNA_ID_3188381,Human_miRNA_ID_3197658,Human_miRNA_ID_3197947,Human_miRNA_ID_3201051,Human_miRNA_ID_3204315,Human_miRNA_ID_3215979 85414 RMVar_ID_85414 Human_SNP_ID_720955191 m1A Human chrX - 73843596 73843596 73843596 CCCCTTCTTTTGGACTTAATATGCATTAATGCAATTGTCCACCTCTTCTTTTAGACTAAGAGTTG CCCCTTCTTTTGGACTTAATATGCATTAATGCGATTGTCCACCTCTTCTTTTAGACTAAGAGTTG T C XIST Ensembl:ENSG00000229807 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs770386223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_738836,Human_RBP_ID_1231860,Human_RBP_ID_1343258,Human_RBP_ID_1406403,Human_RBP_ID_1718271,Human_RBP_ID_2077563,Human_RBP_ID_3927516,Human_RBP_ID_5230956,Human_RBP_ID_5272591,Human_RBP_ID_8020154,Human_RBP_ID_8722556,Human_RBP_ID_10470560,Human_RBP_ID_16931874,Human_RBP_ID_17060479,Human_RBP_ID_18407090,Human_RBP_ID_18924230,Human_RBP_ID_21859988,Human_RBP_ID_22349513,Human_RBP_ID_23105142,Human_RBP_ID_24527691,Human_RBP_ID_26290960,Human_RBP_ID_26745599,Human_RBP_ID_27151144,Human_RBP_ID_27384198,Human_RBP_ID_27795378 85415 RMVar_ID_85415 Human_SNP_ID_720955899 m1A Human chrX - 73845535 73845535 73845535 ATTTATCCCAGTTTCTGTGTAATAGACATGAAAGCCTCCCCTGCCACACCCCACCTCCAATCTTC ATTTATCCCAGTTTCTGTGTAATAGACATGAACGCCTCCCCTGCCACACCCCACCTCCAATCTTC T G XIST Ensembl:ENSG00000229807 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1429386324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258278,Human_RBP_ID_1343317,Human_RBP_ID_1718318,Human_RBP_ID_2077574,Human_RBP_ID_3927567,Human_RBP_ID_5230966,Human_RBP_ID_5252296,Human_RBP_ID_5659648,Human_RBP_ID_8020318,Human_RBP_ID_8722581,Human_RBP_ID_10470660,Human_RBP_ID_16931896,Human_RBP_ID_17095915,Human_RBP_ID_18924295,Human_RBP_ID_21859995,Human_RBP_ID_22122472,Human_RBP_ID_22842846,Human_RBP_ID_23105268,Human_RBP_ID_23204111,Human_RBP_ID_24351993,Human_RBP_ID_24527728,Human_RBP_ID_26291023,Human_RBP_ID_26745636,Human_RBP_ID_27151160,Human_RBP_ID_27384218 85416 RMVar_ID_85416 Human_SNP_ID_720956008 m1A Human chrX - 73845816 73845816 73845816 GACAAGGAAGCCTTCCCCCCGCCCCCACCCCCACTCCCAGTCTTCCTTTCCCTTCCAGCAGGGAG GACAAGGAAGCCTTCCCCCCGCCCCCACCCCCCCTCCCAGTCTTCCTTTCCCTTCCAGCAGGGAG T G XIST Ensembl:ENSG00000229807 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs779141323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_738890,Human_RBP_ID_5084974,Human_RBP_ID_8020339,Human_RBP_ID_10470673,Human_RBP_ID_16931896,Human_RBP_ID_21859998,Human_RBP_ID_22349547,Human_RBP_ID_22842860,Human_RBP_ID_23105268,Human_RBP_ID_23204115,Human_RBP_ID_23302003,Human_RBP_ID_26291032,Human_RBP_ID_26575241,Human_RBP_ID_27151163 Human_miRNA_ID_3212600 85417 RMVar_ID_85417 Human_SNP_ID_720956012 m1A Human chrX - 73845822 73845822 73845822 GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCACCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCCCCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC T G XIST Ensembl:ENSG00000229807 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs773896635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_738890,Human_RBP_ID_5084974,Human_RBP_ID_8020339,Human_RBP_ID_10470673,Human_RBP_ID_16931896,Human_RBP_ID_21859998,Human_RBP_ID_22349547,Human_RBP_ID_22842860,Human_RBP_ID_23105268,Human_RBP_ID_23204115,Human_RBP_ID_23302003,Human_RBP_ID_26291032,Human_RBP_ID_26575241,Human_RBP_ID_27151163 Human_miRNA_ID_3212600 85418 RMVar_ID_85418 Human_SNP_ID_720956585 m1A Human chrX + 73847420 73847418 73847420 CAGGGCAATTGTCTTACTTTTTTTTTTTTTTAATGTTGGCCAGGCTGGTCTCAAACTCCTGGCAG CAGGGCAATTGTCTTACTTTTTTTTTTTTTT__TGTTGGCCAGGCTGGTCTCAAACTCCTGGCAG TAA T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:73847331..73847468 26863410 MeRIP-seq:(Medium) rs1246384937 Functional Loss DEL dbSNP153 32..33 33 - - - 85419 RMVar_ID_85419 Human_SNP_ID_720956587 m1A Human chrX + 73847420 73847420 73847420 CAGGGCAATTGTCTTACTTTTTTTTTTTTTTAATGTTGGCCAGGCTGGTCTCAAACTCCTGGCAG CAGGGCAATTGTCTTACTTTTTTTTTTTTTTATTGTTGGCCAGGCTGGTCTCAAACTCCTGGCAG A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:73847331..73847468 26863410 MeRIP-seq:(Medium) rs1341384191 Functional Loss SNV dbSNP153 33..33 33 - - - 85420 RMVar_ID_85420 Human_SNP_ID_720957310 m1A Human chrX - 73849926 73849926 73849926 CTAGCATCCAGTTCCTCCCCAGCCCTGCTCCCAGCAAACCCCTAGTCTAGCCCCAGCCCTACTCC CTAGCATCCAGTTCCTCCCCAGCCCTGCTCCCGGCAAACCCCTAGTCTAGCCCCAGCCCTACTCC T C XIST Ensembl:ENSG00000229807 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:73849849..73849945 26863410 MeRIP-seq:(Medium) rs368263757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258224,Human_RBP_ID_800084,Human_RBP_ID_3927651,Human_RBP_ID_5072899,Human_RBP_ID_8020601,Human_RBP_ID_8278166,Human_RBP_ID_8722644,Human_RBP_ID_10470765,Human_RBP_ID_16932150,Human_RBP_ID_17095931,Human_RBP_ID_17178945,Human_RBP_ID_18924427,Human_RBP_ID_21860020,Human_RBP_ID_22843033,Human_RBP_ID_23105378,Human_RBP_ID_24527828,Human_RBP_ID_26291125,Human_RBP_ID_27384276,Human_RBP_ID_27795504 85421 RMVar_ID_85421 Human_SNP_ID_720957315 m1A Human chrX + 73849952 73849952 73849952 GTTTGCTGGGAGCAGGGCTGGGGAGGAACTGGATGCTAGGCAGGCAGGATACAACGAAAAATTGA GTTTGCTGGGAGCAGGGCTGGGGAGGAACTGGCTGCTAGGCAGGCAGGATACAACGAAAAATTGA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:73849549..73850043 26863410 MeRIP-seq:(Medium) rs1282617733 Functional Loss SNV dbSNP153 33..33 33 - - - 85422 RMVar_ID_85422 Human_SNP_ID_720957649 m1A Human chrX + 73850821 73850821 73850821 TAGGTGAGGCACCAATACAGAGGAATGGAGGGAGGTTCAGACCACACAGCCAGATATCCAGCACT TAGGTGAGGCACCAATACAGAGGAATGGAGGGCGGTTCAGACCACACAGCCAGATATCCAGCACT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:73850772..73850897 26863196 MeRIP-seq:(Medium) rs1258352547 Functional Loss SNV dbSNP153 33..33 33 - - - 85423 RMVar_ID_85423 Human_SNP_ID_720957855 m1A Human chrX + 73851471 73851471 73851471 CCATCATGATGTGGCCTTCCCGCCACTTGAACACTGCGACAGAACTGGATCCGCCATTTTGGACA CCATCATGATGTGGCCTTCCCGCCACTTGAACGCTGCGACAGAACTGGATCCGCCATTTTGGACA A G lnc-CHIC1-2 RNACentral:URS00008B6C3A lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:73851145..73851551 26863196 MeRIP-seq:(Medium) rs1159070400 Functional Loss SNV dbSNP153 33..33 33 - - - 85424 RMVar_ID_85424 Human_SNP_ID_720990548 m1A Human chrX + 74025098 74025098 74025098 TTAGCGATTTTCAAAGGGGAGAGAGTGTACGAATAGGGTGTGGATCACAGAGATCACATGCTTCA TTAGCGATTTTCAAAGGGGAGAGAGTGTACGAGTAGGGTGTGGATCACAGAGATCACATGCTTCA A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:74025013..74025098 26863196 MeRIP-seq:(Medium) rs1454389513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 85425 RMVar_ID_85425 Human_SNP_ID_721033608 m1A Human chrX - 74264146 74264146 74264146 GGTGTGTCAGGGTTGTTGCCAGGGGCCGGGGGAGGGGGAAAAGGGTCATTGTTTAATGGGAATAG GGTGTGTCAGGGTTGTTGCCAGGGGCCGGGGGGGGGGGAAAAGGGTCATTGTTTAATGGGAATAG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:74264100..74264185 26863196 MeRIP-seq:(Medium) rs1464960437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931860,Human_RBP_ID_8023377,Human_RBP_ID_8227492,Human_RBP_ID_9443183,Human_RBP_ID_18963593,Human_RBP_ID_26797337 85426 RMVar_ID_85426 Human_SNP_ID_721061448 m1A Human chrX + 74421281 74421281 74421281 AGGGTTCAGTAGTTTGGGAAGGGAGCTGGGGGAGGCAGTGGCGGCTGGAGTAGGTAGGCGAGTAA AGGGTTCAGTAGTTTGGGAAGGGAGCTGGGGGTGGCAGTGGCGGCTGGAGTAGGTAGGCGAGTAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:74421231..74421332 26863196 MeRIP-seq:(Medium) rs1360950830 Functional Loss SNV dbSNP153 33..33 33 - - - 85427 RMVar_ID_85427 Human_SNP_ID_721061481 m1A Human chrX + 74421416 74421416 74421416 GGTGTGGAGGAGGGGGAGGAGAGAGAGATGACATGGGGAGAGGAGGAGGGGGGTTGGACGTGGGA GGTGTGGAGGAGGGGGAGGAGAGAGAGATGACCTGGGGAGAGGAGGAGGGGGGTTGGACGTGGGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:74421229..74421607 26863196 MeRIP-seq:(Medium) rs201853949 Functional Loss SNV dbSNP153 33..33 33 - - - 85428 RMVar_ID_85428 Human_SNP_ID_721061482 m1A Human chrX + 74421416 74421416 74421416 GGTGTGGAGGAGGGGGAGGAGAGAGAGATGACATGGGGAGAGGAGGAGGGGGGTTGGACGTGGGA GGTGTGGAGGAGGGGGAGGAGAGAGAGATGACTTGGGGAGAGGAGGAGGGGGGTTGGACGTGGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:74421229..74421607 26863196 MeRIP-seq:(Medium) rs201853949 Functional Loss SNV dbSNP153 33..33 33 - - - 85429 RMVar_ID_85429 Human_SNP_ID_721061577 m1A Human chrX - 74421625 74421625 74421625 GCCTGGCTTTGCAGCGCCATCGCGGCGGGGGGACTGTGGCTGCTTGGGCCAGAGGAGCCGCTTTG GCCTGGCTTTGCAGCGCCATCGCGGCGGGGGGGCTGTGGCTGCTTGGGCCAGAGGAGCCGCTTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:74421579..74421692 32194978 MeRIP-seq:(Medium) rs1029290713 Functional Loss SNV dbSNP153 33..33 33 - - - 85430 RMVar_ID_85430 Human_SNP_ID_721090041 m1A Human chrX - 74583048 74583048 74583048 CAGGGACCACGAAAAGAAACTTGTGCTTCACCAAAGAAAAATATCTAAACATCGAAAAACTTAAA CAGGGACCACGAAAAGAAACTTGTGCTTCACCGAAGAAAAATATCTAAACATCGAAAAACTTAAA T C RLIM Ensembl:ENSG00000131263 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879222169 Functional Loss SNV dbSNP153 33..33 33 - - - 85431 RMVar_ID_85431 Human_SNP_ID_721090078 m1A Human chrX - 74583188 74583188 74583188 TCTTCATATGCTCAAGTCTCCAGAGTCACTCCATTCTAAGGTTGATGAAGCTGTAGCTGTACTAC TCTTCATATGCTCAAGTCTCCAGAGTCACTCCGTTCTAAGGTTGATGAAGCTGTAGCTGTACTAC T C RLIM,PABPC1P3 Ensembl:ENSG00000131263,Ensembl:ENSG00000230673 Protein coding,Pseudogene 3'UTR,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879005635 Functional Loss SNV dbSNP153 33..33 33 - - - 85432 RMVar_ID_85432 Human_SNP_ID_721091627 m1A Human chrX - 74591937 74591926 74591938 CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTCGAGTTCCAGTTCCAGTTCGAGTTCCAGTTCCAGT CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTC____________CAGTTCGAGTTCCAGTTCCAGT GGAACTGGAACTC G RLIM Ensembl:ENSG00000131263 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs763343499 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_16176,Human_RBP_ID_1719194 85433 RMVar_ID_85433 Human_SNP_ID_721091631 m1A Human chrX - 74591937 74591932 74591938 CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTCGAGTTCCAGTTCCAGTTCGAGTTCCAGTTCCAGT CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTC______CAGTTCCAGTTCGAGTTCCAGTTCCAGT GGAACTC G RLIM Ensembl:ENSG00000131263 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs764715887 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_16176,Human_RBP_ID_1719194 85434 RMVar_ID_85434 Human_SNP_ID_721091634 m1A Human chrX - 74591937 74591937 74591937 CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTCGAGTTCCAGTTCCAGTTCGAGTTCCAGTTCCAGT CTGGTGGTGGTAGTAGTTCTGGTTCCAGTTCGGGTTCCAGTTCCAGTTCGAGTTCCAGTTCCAGT T C RLIM Ensembl:ENSG00000131263 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs781417152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16176,Human_RBP_ID_1719194 85435 RMVar_ID_85435 Human_SNP_ID_498773668 m1A Human chr12 - 42084240 42084240 42084240 GTAAGAATGGGGATGGCAAAGGGCAGAGTAAGAGAAAAGATGGAATGAGTGTATGGAAAATTGAG GTAAGAATGGGGATGGCAAAGGGCAGAGTAAGGGAAAAGATGGAATGAGTGTATGGAAAATTGAG T C GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:42084191..42084309 26863196 MeRIP-seq:(Medium) rs1316118236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418897,Human_RBP_ID_6179366,Human_RBP_ID_11931291,Human_RBP_ID_23557926,Human_RBP_ID_24551208 85436 RMVar_ID_85436 Human_SNP_ID_498773681 m1A Human chr12 - 42084278 42084266 42084279 GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGAGAAAGGAGTAAGAATGGGGATGGCAAAGGGCAGA GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGA_____________ATGGGGATGGCAAAGGGCAGA TTCTTACTCCTTTC T GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:42084165..42084356 26863196 MeRIP-seq:(Medium) rs1447636033 Functional Loss DEL dbSNP153 32..44 33 - - - Human_RBP_ID_6179367,Human_RBP_ID_22903555,Human_RBP_ID_23557926,Human_RBP_ID_24551208 85437 RMVar_ID_85437 Human_SNP_ID_498773685 m1A Human chr12 - 42084278 42084274 42084278 GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGAGAAAGGAGTAAGAATGGGGATGGCAAAGGGCAGA GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGAG____GAGTAAGAATGGGGATGGCAAAGGGCAGA CCTTT C GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:42084165..42084356 26863196 MeRIP-seq:(Medium) rs1292976705 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6179367,Human_RBP_ID_22903555,Human_RBP_ID_23557926,Human_RBP_ID_24551208 85438 RMVar_ID_85438 Human_SNP_ID_498773687 m1A Human chr12 - 42084278 42084277 42084279 GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGAGAAAGGAGTAAGAATGGGGATGGCAAAGGGCAGA GAGAGGAAGTGAGAAAAGGGGTGAGGAAAGA__AAGGAGTAAGAATGGGGATGGCAAAGGGCAGA TTC T GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:42084165..42084356 26863196 MeRIP-seq:(Medium) rs1353897825 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6179367,Human_RBP_ID_22903555,Human_RBP_ID_23557926,Human_RBP_ID_24551208 85439 RMVar_ID_85439 Human_SNP_ID_498790742 m1A Human chr12 - 42144668 42144653 42144669 AGTTCGTCGGGGCGGGCGCGGCGGCGGCGGCGAAGGAGGAGCGCGGCCGGGGCGATGCGGCGCTA AGTTCGTCGGGGCGGGCGCGGCGGCGGCGGC________________CGGGGCGATGCGGCGCTA GGCCGCGCTCCTCCTTC G GXYLT1 Ensembl:ENSG00000151233 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:42144428..42144860 26863196 MeRIP-seq:(Medium) rs1381856478 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_4220800,Human_RBP_ID_22436972 85440 RMVar_ID_85440 Human_SNP_ID_498790751 m1A Human chr12 - 42144661 42144661 42144661 CGGGGCGGGCGCGGCGGCGGCGGCGAAGGAGGAGCGCGGCCGGGGCGATGCGGCGCTACCTGCGC CGGGGCGGGCGCGGCGGCGGCGGCGAAGGAGGGGCGCGGCCGGGGCGATGCGGCGCTACCTGCGC T C GXYLT1 Ensembl:ENSG00000151233 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:42144428..42144879 26863196 MeRIP-seq:(Medium) rs1235792165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247378,Human_RBP_ID_22436972 85441 RMVar_ID_85441 Human_SNP_ID_498790753 m1A Human chr12 - 42144667 42144667 42144667 GTTCGTCGGGGCGGGCGCGGCGGCGGCGGCGAAGGAGGAGCGCGGCCGGGGCGATGCGGCGCTAC GTTCGTCGGGGCGGGCGCGGCGGCGGCGGCGAGGGAGGAGCGCGGCCGGGGCGATGCGGCGCTAC T C GXYLT1 Ensembl:ENSG00000151233 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:42144428..42144879 26863196 MeRIP-seq:(Medium) rs539272285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246052,Human_RBP_ID_22436972 85442 RMVar_ID_85442 Human_SNP_ID_498790754 m1A Human chr12 - 42144667 42144667 42144667 GTTCGTCGGGGCGGGCGCGGCGGCGGCGGCGAAGGAGGAGCGCGGCCGGGGCGATGCGGCGCTAC GTTCGTCGGGGCGGGCGCGGCGGCGGCGGCGACGGAGGAGCGCGGCCGGGGCGATGCGGCGCTAC T G GXYLT1 Ensembl:ENSG00000151233 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:42144428..42144879 26863196 MeRIP-seq:(Medium) rs539272285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246052,Human_RBP_ID_22436972 85443 RMVar_ID_85443 Human_SNP_ID_498812990 m1A Human chr12 + 42235871 42235871 42235871 ACTCCCCTGTGTACTATATTCCTTCTTCTTCCAGGTGCCAGGTATTCAGCCTGTTTCTTCTCTTC ACTCCCCTGTGTACTATATTCCTTCTTCTTCCGGGTGCCAGGTATTCAGCCTGTTTCTTCTCTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:42235821..42235937 26863196 MeRIP-seq:(Medium) rs568963303 Functional Loss SNV dbSNP153 33..33 33 - - - 85444 RMVar_ID_85444 Human_SNP_ID_498813702 m1A Human chr12 + 42238198 42238198 42238198 CTTCTTGTCTCCCATGGCTTGGCTATCACCGCACGCCGAGAGTCGCCGCCGCGACCGCTCTGTTT CTTCTTGTCTCCCATGGCTTGGCTATCACCGCGCGCCGAGAGTCGCCGCCGCGACCGCTCTGTTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:42238089..42238352 26863196 MeRIP-seq:(Medium) rs773156618 Functional Loss SNV dbSNP153 33..33 33 - - - 85445 RMVar_ID_85445 Human_SNP_ID_498832663 m1A Human chr12 - 42313749 42313749 42313749 TTTTTCTTTATTTAAGTGAGGAAGTAGAAGAAAGTGAAGATGAAGGGGAGGATCCTGCTCTTGAC TTTTTCTTTATTTAAGTGAGGAAGTAGAAGAAGGTGAAGATGAAGGGGAGGATCCTGCTCTTGAC T C ZCRB1 Ensembl:ENSG00000139168 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:42313025..42317377 32194978 MeRIP-seq:(Medium) rs1224370693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194382,Human_RBP_ID_1479524,Human_RBP_ID_2335003,Human_RBP_ID_6179918,Human_RBP_ID_9344234,Human_RBP_ID_9364827,Human_RBP_ID_23113328,Human_RBP_ID_23558201,Human_RBP_ID_24543058,Human_RBP_ID_26321308,Human_RBP_ID_27806542 Human_Splice_Rec_1356618,Human_Splice_Rec_1356619,Human_Splice_Rec_1356632,Human_Splice_Rec_1356633,Human_Splice_Rec_1356644 Human_miRNA_ID_2195583 RMVar_hsa_circ_86483,RMVar_hsa_circ_60642,RMVar_hsa_circ_155940 85446 RMVar_ID_85446 Human_SNP_ID_498832731 m1A Human chr12 - 42313911 42313911 42313911 GAGAACGTGAGCCTCCAAAGAAGAAAGAAAAAAAGAAAAAAAAGAAAGCTCCTGAACCAGAAGAA GAGAACGTGAGCCTCCAAAGAAGAAAGAAAAAGAGAAAAAAAAGAAAGCTCCTGAACCAGAAGAA T C ZCRB1 Ensembl:ENSG00000139168 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:42313691..42313936;chr12:42313701..42314000 26863196 MeRIP-seq:(Medium) rs1466432981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1479526,Human_RBP_ID_22903609,Human_RBP_ID_24543060,Human_RBP_ID_26322781 Human_Splice_Rec_1356616,Human_Splice_Rec_1356617,Human_Splice_Rec_1356630,Human_Splice_Rec_1356631,Human_Splice_Rec_1356642,Human_Splice_Rec_1356643 Human_miRNA_ID_2292258,Human_miRNA_ID_2357603,Human_miRNA_ID_3060042 RMVar_hsa_circ_86483,RMVar_hsa_circ_60642,RMVar_hsa_circ_155940 85447 RMVar_ID_85447 Human_SNP_ID_498834049 m1A Human chr12 + 42319404 42319404 42319404 TTTGGTTCTGTAAGTTGCCTATTCTTTGTCCCACTGTCAGTATCCTTGATGATTTGGCTCCCATC TTTGGTTCTGTAAGTTGCCTATTCTTTGTCCCCCTGTCAGTATCCTTGATGATTTGGCTCCCATC A C PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:42319399..42319508 26863196 MeRIP-seq:(Medium) rs1044109579 Functional Loss SNV dbSNP153 33..33 33 - - - 85448 RMVar_ID_85448 Human_SNP_ID_498834050 m1A Human chr12 + 42319404 42319404 42319404 TTTGGTTCTGTAAGTTGCCTATTCTTTGTCCCACTGTCAGTATCCTTGATGATTTGGCTCCCATC TTTGGTTCTGTAAGTTGCCTATTCTTTGTCCCGCTGTCAGTATCCTTGATGATTTGGCTCCCATC A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:42319399..42319508 26863196 MeRIP-seq:(Medium) rs1044109579 Functional Loss SNV dbSNP153 33..33 33 - - - 85449 RMVar_ID_85449 Human_SNP_ID_498835640 m1A Human chr12 - 42326018 42326018 42326018 GCGCCTGACCCCTCCCAGGACTCGTGATGCCAAGGCCGCTGCGAGCGGCTACGAAGAGTCGGGGT GCGCCTGACCCCTCCCAGGACTCGTGATGCCAGGGCCGCTGCGAGCGGCTACGAAGAGTCGGGGT T C ZCRB1 Ensembl:ENSG00000139168 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:42325967..42326075 32194978 MeRIP-seq:(Medium) rs1005435506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246586,Human_RBP_ID_8374922,Human_RBP_ID_9323035,Human_RBP_ID_26321310,Human_RBP_ID_26806592,Human_RBP_ID_26905948 Human_Splice_Rec_1356607,Human_Splice_Rec_1356621,Human_Splice_Rec_1356635,Human_Splice_Rec_1356645,Human_Splice_Rec_1356647 85450 RMVar_ID_85450 Human_SNP_ID_498835641 m1A Human chr12 - 42326018 42326018 42326018 GCGCCTGACCCCTCCCAGGACTCGTGATGCCAAGGCCGCTGCGAGCGGCTACGAAGAGTCGGGGT GCGCCTGACCCCTCCCAGGACTCGTGATGCCACGGCCGCTGCGAGCGGCTACGAAGAGTCGGGGT T G ZCRB1 Ensembl:ENSG00000139168 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:42325967..42326075 32194978 MeRIP-seq:(Medium) rs1005435506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246586,Human_RBP_ID_8374922,Human_RBP_ID_9323035,Human_RBP_ID_26321310,Human_RBP_ID_26806592,Human_RBP_ID_26905948 Human_Splice_Rec_1356607,Human_Splice_Rec_1356621,Human_Splice_Rec_1356635,Human_Splice_Rec_1356645,Human_Splice_Rec_1356647 85451 RMVar_ID_85451 Human_SNP_ID_498835665 m1A Human chr12 - 42326061 42326061 42326061 AACAGTCGGGAAGAAGCACCGTGGCTGCTATTATCTGCTCTCCGCGCCTGACCCCTCCCAGGACT AACAGTCGGGAAGAAGCACCGTGGCTGCTATTGTCTGCTCTCCGCGCCTGACCCCTCCCAGGACT T C ZCRB1 Ensembl:ENSG00000139168 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:42325968..42326100 26863196 MeRIP-seq:(Medium) rs1396880927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_419027,Human_RBP_ID_1470895,Human_RBP_ID_4246586,Human_RBP_ID_5416992,Human_RBP_ID_5461776,Human_RBP_ID_5491465,Human_RBP_ID_6179957,Human_RBP_ID_17684325,Human_RBP_ID_18206325,Human_RBP_ID_26321310,Human_RBP_ID_27421583 85452 RMVar_ID_85452 Human_SNP_ID_498835743 m1A Human chr12 - 42326231 42326231 42326231 GCATCCATCTCTGGGAAAGGTAAAAAGCGCTCACCGACTCTGGCCCTCCGGGAGACCCCGTAAAT GCATCCATCTCTGGGAAAGGTAAAAAGCGCTCGCCGACTCTGGCCCTCCGGGAGACCCCGTAAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:42326176..42326275;chr12:42326176..42329872;chr12:42326176..42326297;chr12:42326176..42326250 26863196 MeRIP-seq:(Medium) rs1300121838 Functional Loss SNV dbSNP153 33..33 33 - - - 85453 RMVar_ID_85453 Human_SNP_ID_498838247 m1A Human chr12 - 42335878 42335877 42335878 GACCACATTTCGTCTCTTCTGTAAGCCACTAAAGAAAAAAAAAAGAATTATGGATTTTATACTAG GACCACATTTCGTCTCTTCTGTAAGCCACTAA_GAAAAAAAAAAGAATTATGGATTTTATACTAG CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:42335876..42335975 32194978 MeRIP-seq:(Medium) rs772455636 Functional Loss DEL dbSNP153 33..33 33 - - - 85454 RMVar_ID_85454 Human_SNP_ID_499184456 m1A Human chr12 - 43758703 43758703 43758703 ACCGAGGTAGACGGGGTCGAGTTTCTTGCGCGATGGTGGGCTTGTATGTGTGTGTGTGTGTGTGT ACCGAGGTAGACGGGGTCGAGTTTCTTGCGCGGTGGTGGGCTTGTATGTGTGTGTGTGTGTGTGT T C PUS7L Ensembl:ENSG00000129317 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:43758504..43758745 26863196 MeRIP-seq:(Medium) rs536892975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23558839 Human_Splice_Rec_1357173,Human_Splice_Rec_1357203,Human_Splice_Rec_1357229 RMVar_hsa_circ_104841,RMVar_hsa_circ_155975 85455 RMVar_ID_85455 Human_SNP_ID_499191645 m1A Human chr12 + 43789302 43789302 43789302 CTCAGTTCGTGTGAGATCTGGTGGCTTAAAAGAGTCTGCTCCCCCTTTGCCTTCCATTGTGATTG CTCAGTTCGTGTGAGATCTGGTGGCTTAAAAGCGTCTGCTCCCCCTTTGCCTTCCATTGTGATTG A C IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:43789174..43789347 26863196 MeRIP-seq:(Medium) rs948939629 Functional Loss SNV dbSNP153 33..33 33 - - - 85456 RMVar_ID_85456 Human_SNP_ID_499191646 m1A Human chr12 + 43789302 43789302 43789302 CTCAGTTCGTGTGAGATCTGGTGGCTTAAAAGAGTCTGCTCCCCCTTTGCCTTCCATTGTGATTG CTCAGTTCGTGTGAGATCTGGTGGCTTAAAAGGGTCTGCTCCCCCTTTGCCTTCCATTGTGATTG A G IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:43789174..43789347 26863196 MeRIP-seq:(Medium) rs948939629 Functional Loss SNV dbSNP153 33..33 33 - - - 85457 RMVar_ID_85457 Human_SNP_ID_499536808 m1A Human chr12 - 45215966 45215966 45215966 AGAGGGAGTAGTGCGATCCTGCGCGCGGGGGAACTAGCTGGAGGGCAAGGCGGGAACACGTGAGT AGAGGGAGTAGTGCGATCCTGCGCGCGGGGGATCTAGCTGGAGGGCAAGGCGGGAACACGTGAGT T A PLEKHA8P1 Ensembl:ENSG00000134297 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:45190865..45215996;chr12:45215889..45215986 26863196 MeRIP-seq:(Medium) rs778584302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4248572,Human_RBP_ID_5172958,Human_RBP_ID_5556002,Human_RBP_ID_9417073 Human_Splice_Rec_1358053,Human_Splice_Rec_1358057,Human_Splice_Rec_1358059 85458 RMVar_ID_85458 Human_SNP_ID_499536809 m1A Human chr12 - 45215966 45215966 45215966 AGAGGGAGTAGTGCGATCCTGCGCGCGGGGGAACTAGCTGGAGGGCAAGGCGGGAACACGTGAGT AGAGGGAGTAGTGCGATCCTGCGCGCGGGGGAGCTAGCTGGAGGGCAAGGCGGGAACACGTGAGT T C PLEKHA8P1 Ensembl:ENSG00000134297 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:45190865..45215996;chr12:45215889..45215986 26863196 MeRIP-seq:(Medium) rs778584302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4248572,Human_RBP_ID_5172958,Human_RBP_ID_5556002,Human_RBP_ID_9417073 Human_Splice_Rec_1358053,Human_Splice_Rec_1358057,Human_Splice_Rec_1358059 85459 RMVar_ID_85459 Human_SNP_ID_499536820 m1A Human chr12 + 45215987 45215987 45215987 CCTCCAGCTAGTTCCCCCGCGCGCAGGATCGCACTACTCCCTCTGCAGTCTCGCCTGCCGACTTC CCTCCAGCTAGTTCCCCCGCGCGCAGGATCGCCCTACTCCCTCTGCAGTCTCGCCTGCCGACTTC A C ANO6 Ensembl:ENSG00000177119 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:45190914..45216041 26863196 MeRIP-seq:(Medium) rs1469252072 Functional Loss SNV dbSNP153 33..33 33 - - - 85460 RMVar_ID_85460 Human_SNP_ID_499536911 m1A Human chr12 - 45216161 45216161 45216161 GAGCCCAGCCAGCGCCGGGGAAAGCCGAGCCGAGGCACCCACCGACCGGAGCCCAGAGCCGGAGG GAGCCCAGCCAGCGCCGGGGAAAGCCGAGCCGCGGCACCCACCGACCGGAGCCCAGAGCCGGAGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:45216086..45216375 26863196 MeRIP-seq:(Medium) rs1264838888 Functional Loss SNV dbSNP153 33..33 33 - - - 85461 RMVar_ID_85461 Human_SNP_ID_499536945 m1A Human chr12 + 45216284 45216284 45216284 AGCCGCGCCGTTCTGGAACCCGGGAGCCCCCAACTTCGCGCCAAGTTCGGAGCCGCCTTCTGAGG AGCCGCGCCGTTCTGGAACCCGGGAGCCCCCACCTTCGCGCCAAGTTCGGAGCCGCCTTCTGAGG A C ANO6 Ensembl:ENSG00000177119 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45216118..45216386 26863196 MeRIP-seq:(Medium) rs540609555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_419460,Human_RBP_ID_4246058,Human_RBP_ID_22436368 85462 RMVar_ID_85462 Human_SNP_ID_499536946 m1A Human chr12 + 45216284 45216284 45216284 AGCCGCGCCGTTCTGGAACCCGGGAGCCCCCAACTTCGCGCCAAGTTCGGAGCCGCCTTCTGAGG AGCCGCGCCGTTCTGGAACCCGGGAGCCCCCAGCTTCGCGCCAAGTTCGGAGCCGCCTTCTGAGG A G ANO6 Ensembl:ENSG00000177119 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45216118..45216386 26863196 MeRIP-seq:(Medium) rs540609555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_419460,Human_RBP_ID_4246058,Human_RBP_ID_22436368 85463 RMVar_ID_85463 Human_SNP_ID_499559077 m1A Human chr12 + 45307575 45307572 45307575 GGTGGAGAAGTCAGTATGCAGTGGGATATGTGAACCTGGAGTAAGAGTTAAAGAGGGGGGCCCAA GGTGGAGAAGTCAGTATGCAGTGGGATATG___ACCTGGAGTAAGAGTTAAAGAGGGGGGCCCAA GTGA G ANO6 Ensembl:ENSG00000177119 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45307573..45307851 26863196 MeRIP-seq:(Medium) rs1418036505 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_6505,RMVar_hsa_circ_47192,RMVar_hsa_circ_107033,RMVar_hsa_circ_5563,RMVar_hsa_circ_348963,RMVar_hsa_circ_72973,RMVar_hsa_circ_34990,RMVar_hsa_circ_156022 85464 RMVar_ID_85464 Human_SNP_ID_499584353 m1A Human chr12 + 45413249 45413249 45413249 TTTAGGAGGCTACAGCAGGTAACCCAGACAACAAGTGATAGGTGCCTAAATAGTGGGCATAGGAG TTTAGGAGGCTACAGCAGGTAACCCAGACAACCAGTGATAGGTGCCTAAATAGTGGGCATAGGAG A C ANO6 Ensembl:ENSG00000177119 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:45413201..45413353 26863196 MeRIP-seq:(Medium) rs1048416106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34990,RMVar_hsa_circ_68423,RMVar_hsa_circ_90302,RMVar_hsa_circ_156029,RMVar_hsa_circ_85655,RMVar_hsa_circ_97007,RMVar_hsa_circ_156030,RMVar_hsa_circ_340494,RMVar_hsa_circ_156032,RMVar_hsa_circ_156033,RMVar_hsa_circ_328966 85465 RMVar_ID_85465 Human_SNP_ID_499656379 m1A Human chr12 + 45726973 45726973 45726973 CATCGTCATCCCCGGCTCGGATCCCGGCCGCGACCCGCCAGGGCCGCCGGAGTCCGCGAATACCG CATCGTCATCCCCGGCTCGGATCCCGGCCGCGGCCCGCCAGGGCCGCCGGAGTCCGCGAATACCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:45726926..45727054 26863196 MeRIP-seq:(Medium) rs1324420788 Functional Loss SNV dbSNP153 33..33 33 - - - 85466 RMVar_ID_85466 Human_SNP_ID_499656383 m1A Human chr12 + 45726980 45726980 45726980 ATCCCCGGCTCGGATCCCGGCCGCGACCCGCCAGGGCCGCCGGAGTCCGCGAATACCGCCCGCTC ATCCCCGGCTCGGATCCCGGCCGCGACCCGCCGGGGCCGCCGGAGTCCGCGAATACCGCCCGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45726934..45727079 26863196 MeRIP-seq:(Medium) rs1222291673 Functional Loss SNV dbSNP153 33..33 33 - - - 85467 RMVar_ID_85467 Human_SNP_ID_499657202 m1A Human chr12 - 45729354 45729354 45729354 GCTGCCGGGGGCGCGCGAGCGGGCGACGGGCAAGGCGAGCCGATGGTGAGGGGTCTGGGCGGCCA GCTGCCGGGGGCGCGCGAGCGGGCGACGGGCAGGGCGAGCCGATGGTGAGGGGTCTGGGCGGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45729306..45729473 26863196 MeRIP-seq:(Medium) rs1285468121 Functional Loss SNV dbSNP153 33..33 33 - - - 85468 RMVar_ID_85468 Human_SNP_ID_499657377 m1A Human chr12 + 45729703 45729679 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCG________________________CCGCCGGCCCATGACTGAGCCCCGCCGCCGCC GCCGCCGCCGCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs1179851568 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_18417435 85469 RMVar_ID_85469 Human_SNP_ID_499657389 m1A Human chr12 + 45729703 45729694 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCG_________CCGCCGGCCCATGACTGAGCCCCGCCGCCGCC GCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs1197790098 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_18417435 85470 RMVar_ID_85470 Human_SNP_ID_499657395 m1A Human chr12 + 45729703 45729697 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCG______CCGCCGGCCCATGACTGAGCCCCGCCGCCGCC GCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs1170774909 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_18417435 85471 RMVar_ID_85471 Human_SNP_ID_499657400 m1A Human chr12 + 45729703 45729703 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGGCCCATGACTGAGCCCCGCCGCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs868266376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417435 85472 RMVar_ID_85472 Human_SNP_ID_499657401 m1A Human chr12 + 45729703 45729703 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGGCCCATGACTGAGCCCCGCCGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs868266376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417435 85473 RMVar_ID_85473 Human_SNP_ID_499657402 m1A Human chr12 + 45729703 45729703 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCGGCCCATGACTGAGCCCCGCCGCCGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs868266376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417435 85474 RMVar_ID_85474 Human_SNP_ID_499657410 m1A Human chr12 - 45729715 45729715 45729715 CATTCCTCGGCCGGCGGCGGCGGGGCTCAGTCATGGGCCGGCGGTGGCGGCGGCGGCGGCGGCGG CATTCCTCGGCCGGCGGCGGCGGGGCTCAGTCTTGGGCCGGCGGTGGCGGCGGCGGCGGCGGCGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45729664..45729836 26863196 MeRIP-seq:(Medium) rs1328339855 Functional Loss SNV dbSNP153 33..33 33 - - - 85475 RMVar_ID_85475 Human_SNP_ID_499657411 m1A Human chr12 - 45729715 45729715 45729715 CATTCCTCGGCCGGCGGCGGCGGGGCTCAGTCATGGGCCGGCGGTGGCGGCGGCGGCGGCGGCGG CATTCCTCGGCCGGCGGCGGCGGGGCTCAGTCGTGGGCCGGCGGTGGCGGCGGCGGCGGCGGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45729664..45729836 26863196 MeRIP-seq:(Medium) rs1328339855 Functional Loss SNV dbSNP153 33..33 33 - - - 85476 RMVar_ID_85476 Human_SNP_ID_499686278 m1A Human chr12 + 45851534 45851533 45851535 GTTCAGTTGGTCCCAAGTGCAATGCCACCCTCAGGGGGAGTACAAACTGTGCCCATTTCGAACTT GTTCAGTTGGTCCCAAGTGCAATGCCACCCTC__GGGGAGTACAAACTGTGCCCATTTCGAACTT CAG C ARID2 Ensembl:ENSG00000189079 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:45851448..45851535 32194978 MeRIP-seq:(Medium) rs1555155252 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1973263,Human_miRNA_ID_1975439,Human_miRNA_ID_2613242 Clinvar_Rec_447 RMVar_hsa_circ_10458,RMVar_hsa_circ_303407,RMVar_hsa_circ_363903,RMVar_hsa_circ_293483,RMVar_hsa_circ_327759,RMVar_hsa_circ_312092,RMVar_hsa_circ_88125,RMVar_hsa_circ_156056,RMVar_hsa_circ_156057,RMVar_hsa_circ_156058,RMVar_hsa_circ_108547,RMVar_hsa_circ_156059,RMVar_hsa_circ_156060,RMVar_hsa_circ_69773,RMVar_hsa_circ_58567,RMVar_hsa_circ_156062,RMVar_hsa_circ_127224,RMVar_hsa_circ_286363,RMVar_hsa_circ_74311,RMVar_hsa_circ_376615,RMVar_hsa_circ_156063 85477 RMVar_ID_85477 Human_SNP_ID_499686279 m1A Human chr12 + 45851534 45851534 45851534 GTTCAGTTGGTCCCAAGTGCAATGCCACCCTCAGGGGGAGTACAAACTGTGCCCATTTCGAACTT GTTCAGTTGGTCCCAAGTGCAATGCCACCCTCGGGGGGAGTACAAACTGTGCCCATTTCGAACTT A G ARID2 Ensembl:ENSG00000189079 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:45851448..45851535 32194978 MeRIP-seq:(Medium) rs766110823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1973263,Human_miRNA_ID_1975439,Human_miRNA_ID_2613242 RMVar_hsa_circ_10458,RMVar_hsa_circ_303407,RMVar_hsa_circ_363903,RMVar_hsa_circ_293483,RMVar_hsa_circ_327759,RMVar_hsa_circ_312092,RMVar_hsa_circ_88125,RMVar_hsa_circ_156056,RMVar_hsa_circ_156057,RMVar_hsa_circ_156058,RMVar_hsa_circ_108547,RMVar_hsa_circ_156059,RMVar_hsa_circ_156060,RMVar_hsa_circ_69773,RMVar_hsa_circ_58567,RMVar_hsa_circ_156062,RMVar_hsa_circ_127224,RMVar_hsa_circ_286363,RMVar_hsa_circ_74311,RMVar_hsa_circ_376615,RMVar_hsa_circ_156063 85478 RMVar_ID_85478 Human_SNP_ID_499697305 m1A Human chr12 - 45898295 45898295 45898295 TCATAATGGAACTCTCTACCCACTTAACAGTAACTCTCCATTCCTGAACTACCCCCAGCCCCAGT TCATAATGGAACTCTCTACCCACTTAACAGTAGCTCTCCATTCCTGAACTACCCCCAGCCCCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:45898245..45898328 26863196 MeRIP-seq:(Medium) rs754405171 Functional Loss SNV dbSNP153 33..33 33 - - - 85479 RMVar_ID_85479 Human_SNP_ID_499697306 m1A Human chr12 - 45898295 45898295 45898295 TCATAATGGAACTCTCTACCCACTTAACAGTAACTCTCCATTCCTGAACTACCCCCAGCCCCAGT TCATAATGGAACTCTCTACCCACTTAACAGTACCTCTCCATTCCTGAACTACCCCCAGCCCCAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:45898245..45898328 26863196 MeRIP-seq:(Medium) rs754405171 Functional Loss SNV dbSNP153 33..33 33 - - - 85480 RMVar_ID_85480 Human_SNP_ID_499708230 m1A Human chr12 - 45941598 45941598 45941598 TTGGGAGGGTATAATGAAGAATTCTCTTTTGGAAGTAGAATGGTGGTGGTTTTTGGGAGCGGGGA TTGGGAGGGTATAATGAAGAATTCTCTTTTGGGAGTAGAATGGTGGTGGTTTTTGGGAGCGGGGA T C SCAF11 Ensembl:ENSG00000139218 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:45941594..45941682 26863196 MeRIP-seq:(Medium) rs1261079393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9415854 RMVar_hsa_circ_10666,RMVar_hsa_circ_58541,RMVar_hsa_circ_288652,RMVar_hsa_circ_57793,RMVar_hsa_circ_57537,RMVar_hsa_circ_83703,RMVar_hsa_circ_156074,RMVar_hsa_circ_156078,RMVar_hsa_circ_270042,RMVar_hsa_circ_156077,RMVar_hsa_circ_59832,RMVar_hsa_circ_77242,RMVar_hsa_circ_156079,RMVar_hsa_circ_28415 85481 RMVar_ID_85481 Human_SNP_ID_499769088 m1A Human chr12 - 46184230 46184230 46184230 ATAACGAGATAAAGCTTTCAGGTACAAGCTGAAGGTGGGGTGTCTAACAACTAAAAACTATCACT ATAACGAGATAAAGCTTTCAGGTACAAGCTGATGGTGGGGTGTCTAACAACTAAAAACTATCACT T A SLC38A1 Ensembl:ENSG00000111371 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs924973668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6185714,Human_RBP_ID_11942590,Human_RBP_ID_17238295,Human_RBP_ID_17471139,Human_RBP_ID_22383102,Human_RBP_ID_23559916 Human_miRNA_ID_547158 RMVar_hsa_circ_156085,RMVar_hsa_circ_105387 85482 RMVar_ID_85482 Human_SNP_ID_499770151 m1A Human chr12 - 46188759 46188759 46188759 CTCCAAGATTTGAGATCAATTTAGGGATTGTGAAATTTTTTTTTCAAATTTCATACAATCATATT CTCCAAGATTTGAGATCAATTTAGGGATTGTGTAATTTTTTTTTCAAATTTCATACAATCATATT T A SLC38A1 Ensembl:ENSG00000111371 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61923107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_419779,Human_RBP_ID_1471560,Human_RBP_ID_2337721,Human_RBP_ID_6185899,Human_RBP_ID_8068135,Human_RBP_ID_8375845,Human_RBP_ID_11942891,Human_RBP_ID_17186126,Human_RBP_ID_17238349,Human_RBP_ID_17354214,Human_RBP_ID_17471206,Human_RBP_ID_17819305,Human_RBP_ID_23559962,Human_RBP_ID_24407067,Human_RBP_ID_27629238 Human_miRNA_ID_1522258 RMVar_hsa_circ_156085,RMVar_hsa_circ_105387 85483 RMVar_ID_85483 Human_SNP_ID_499770191 m1A Human chr12 - 46188954 46188954 46188954 GTGACGAAGGCCACTGAAACCCGCCGAGAAAAAGAAACATCCCTGTTGTCTGCTCAGTCAAGTCC GTGACGAAGGCCACTGAAACCCGCCGAGAAAAGGAAACATCCCTGTTGTCTGCTCAGTCAAGTCC T C SLC38A1 Ensembl:ENSG00000111371 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:46188905..46189032 26863196 MeRIP-seq:(Medium) rs1199519631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_419787,Human_RBP_ID_4254791,Human_RBP_ID_11942903,Human_RBP_ID_22757168,Human_RBP_ID_22912150,Human_RBP_ID_24971259 RMVar_hsa_circ_156085,RMVar_hsa_circ_105387 85484 RMVar_ID_85484 Human_SNP_ID_499771908 m1A Human chr12 + 46195265 46195265 46195265 TCCAGAATCTGTTTGCCTGGGTATCACCAGCAAAGGCTGCAGAATAGCAAATATTGCTGCCTGAT TCCAGAATCTGTTTGCCTGGGTATCACCAGCAGAGGCTGCAGAATAGCAAATATTGCTGCCTGAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:46195244..46195344 32194978 MeRIP-seq:(Medium) rs1402873336 Functional Loss SNV dbSNP153 33..33 33 - - - 85485 RMVar_ID_85485 Human_SNP_ID_499789476 m1A Human chr12 + 46268619 46268619 46268619 TTTACCCTCGGCAGTTTGATGTCCTTTGTGTCAAGGTCTGGCTGCGGAGGCCGGGAAAATGTGGC TTTACCCTCGGCAGTTTGATGTCCTTTGTGTCCAGGTCTGGCTGCGGAGGCCGGGAAAATGTGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:46268571..46269094;chr12:46268571..46268722 26863196 MeRIP-seq:(Medium) rs1473922167 Functional Loss SNV dbSNP153 33..33 33 - - - 85486 RMVar_ID_85486 Human_SNP_ID_499789541 m1A Human chr12 - 46268801 46268801 46268801 TGGGGGTTGGTGGTGAGGGGAGATTCTGATGCAATCGGCCCGGAAAGGAGGAGAGCCAGGCGAGC TGGGGGTTGGTGGTGAGGGGAGATTCTGATGCTATCGGCCCGGAAAGGAGGAGAGCCAGGCGAGC T A SLC38A1 Ensembl:ENSG00000111371 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:46268751..46269125 26863196 MeRIP-seq:(Medium) rs1039293550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4222501,Human_RBP_ID_23560120 RMVar_hsa_circ_82469,RMVar_hsa_circ_117672,RMVar_hsa_circ_156109,RMVar_hsa_circ_156110 85487 RMVar_ID_85487 Human_SNP_ID_499789612 m1A Human chr12 + 46268965 46268965 46268965 CCGCAACCATGGCTTGTGATGGTTTAACGCGGACAGGCCATTCCTCCCCGTCCCGCGCGCGGTCT CCGCAACCATGGCTTGTGATGGTTTAACGCGGCCAGGCCATTCCTCCCCGTCCCGCGCGCGGTCT A C lnc-ARID2-8 RNACentral:URS00008BCCFF lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:46268601..46269111 26863196 MeRIP-seq:(Medium) rs1413094830 Functional Loss SNV dbSNP153 33..33 33 - - - 85488 RMVar_ID_85488 Human_SNP_ID_499818655 m1A Human chr12 + 46372073 46372073 46372073 CGGAAAGAAAACTGATGCAATATCGATCGTCGATTGTCAAATGTTCCCAACTCGTCTTCCCCAAT CGGAAAGAAAACTGATGCAATATCGATCGTCGCTTGTCAAATGTTCCCAACTCGTCTTCCCCAAT A C AC025031.2 Ensembl:ENSG00000258096 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:46372070..46372194 26863196 MeRIP-seq:(Medium) rs1302688807 Functional Loss SNV dbSNP153 33..33 33 - - - 85489 RMVar_ID_85489 Human_SNP_ID_499818716 m1A Human chr12 + 46372242 46372242 46372242 AGACTTGCCGCAGCAGAGCCGCTGGCCGGGCTAGCTCCCCTCCCCCTAATGGGAAGATGCGGCTC AGACTTGCCGCAGCAGAGCCGCTGGCCGGGCTTGCTCCCCTCCCCCTAATGGGAAGATGCGGCTC A T AC025031.2 Ensembl:ENSG00000258096 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:46372234..46372457 26863196 MeRIP-seq:(Medium) rs972744697 Functional Loss SNV dbSNP153 33..33 33 - - - 85490 RMVar_ID_85490 Human_SNP_ID_499818756 m1A Human chr12 - 46372367 46372350 46372367 TTTCGAGGCGGGCGTTGTCGGTTGGGCTGGCCAGCCTTCCACCCTGGCCCGCCGCGCGGGTGTCG TTTCGAGGCGGGCGTTGTCGGTTGGGCTGGCC_________________CGCCGCGCGGGTGTCG GGGCCAGGGTGGAAGGCT G SLC38A2 Ensembl:ENSG00000134294 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:46372364..46372486 26863196 MeRIP-seq:(Medium) rs1565831573 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_874430,Human_RBP_ID_3420528,Human_RBP_ID_5347242,Human_RBP_ID_18457246,Human_RBP_ID_26776794 Human_Splice_Rec_1358931 RMVar_hsa_circ_124291,RMVar_hsa_circ_156129 85491 RMVar_ID_85491 Human_SNP_ID_499818766 m1A Human chr12 - 46372367 46372367 46372367 TTTCGAGGCGGGCGTTGTCGGTTGGGCTGGCCAGCCTTCCACCCTGGCCCGCCGCGCGGGTGTCG TTTCGAGGCGGGCGTTGTCGGTTGGGCTGGCCGGCCTTCCACCCTGGCCCGCCGCGCGGGTGTCG T C SLC38A2 Ensembl:ENSG00000134294 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:46372364..46372486 26863196 MeRIP-seq:(Medium) rs1163269558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874430,Human_RBP_ID_3420528,Human_RBP_ID_5347242,Human_RBP_ID_18457246,Human_RBP_ID_26776794 Human_Splice_Rec_1358931 RMVar_hsa_circ_124291,RMVar_hsa_circ_156129 85492 RMVar_ID_85492 Human_SNP_ID_499818880 m1A Human chr12 + 46372696 46372696 46372696 TCCGGCGTCCGCCGTGTCAAGGGAAAGGCGCGAGCGTGCGGTAACGCGTGGTCGGGCTGCTGCTA TCCGGCGTCCGCCGTGTCAAGGGAAAGGCGCGTGCGTGCGGTAACGCGTGGTCGGGCTGCTGCTA A T AC025031.2 Ensembl:ENSG00000258096 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:46372601..46372800 26863410 MeRIP-seq:(Medium) rs1226222513 Functional Loss SNV dbSNP153 33..33 33 - - - 85493 RMVar_ID_85493 Human_SNP_ID_499818893 m1A Human chr12 - 46372721 46372721 46372721 CCTTAGAACGCCTTTCCAGTACTGCTAGCAGCAGCCCGACCACGCGTTACCGCACGCTCGCGCCT CCTTAGAACGCCTTTCCAGTACTGCTAGCAGCTGCCCGACCACGCGTTACCGCACGCTCGCGCCT T A SLC38A2 Ensembl:ENSG00000134294 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:46372626..46372775;chr12:46372552..46372775;chr12:46372273..46372789;chr12:46372564..46372775 26863196 MeRIP-seq:(Medium) rs1384384764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810464,Human_RBP_ID_1471944,Human_RBP_ID_1795394,Human_RBP_ID_4222721,Human_RBP_ID_6187293,Human_RBP_ID_8376198,Human_RBP_ID_11946549,Human_RBP_ID_18626858,Human_RBP_ID_22039220 Human_miRNA_ID_2579776 RMVar_hsa_circ_124291,RMVar_hsa_circ_156129 85494 RMVar_ID_85494 Human_SNP_ID_499818894 m1A Human chr12 - 46372721 46372721 46372721 CCTTAGAACGCCTTTCCAGTACTGCTAGCAGCAGCCCGACCACGCGTTACCGCACGCTCGCGCCT CCTTAGAACGCCTTTCCAGTACTGCTAGCAGCGGCCCGACCACGCGTTACCGCACGCTCGCGCCT T C SLC38A2 Ensembl:ENSG00000134294 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:46372626..46372775;chr12:46372552..46372775;chr12:46372273..46372789;chr12:46372564..46372775 26863196 MeRIP-seq:(Medium) rs1384384764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810464,Human_RBP_ID_1471944,Human_RBP_ID_1795394,Human_RBP_ID_4222721,Human_RBP_ID_6187293,Human_RBP_ID_8376198,Human_RBP_ID_11946549,Human_RBP_ID_18626858,Human_RBP_ID_22039220 Human_miRNA_ID_2579776 RMVar_hsa_circ_124291,RMVar_hsa_circ_156129 85495 RMVar_ID_85495 Human_SNP_ID_499821564 m1A Human chr12 + 46383190 46383190 46383190 GCAAGGCCGCGTGGCGGCTTGGAGCCGCGCGAAGGAAGCGAGGGCTGGCGGCCCCAGGGCAAAGG GCAAGGCCGCGTGGCGGCTTGGAGCCGCGCGATGGAAGCGAGGGCTGGCGGCCCCAGGGCAAAGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:46383155..46383284 26863196 MeRIP-seq:(Medium) rs1483092144 Functional Loss SNV dbSNP153 33..33 33 - - - 85496 RMVar_ID_85496 Human_SNP_ID_499827442 m1A Human chr12 + 46405853 46405853 46405853 TGGCACGAGTTGGACGCCAGTTAGATGTGGGGAGGTGAGATGGATGTAGAGGAAGGAGAGGAAGA TGGCACGAGTTGGACGCCAGTTAGATGTGGGGTGGTGAGATGGATGTAGAGGAAGGAGAGGAAGA A T AC008014.1,AC025031.5 Ensembl:ENSG00000257261,Ensembl:ENSG00000278896 lincRNA,Other intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:46405805..46405888 26863196 MeRIP-seq:(Medium) rs925498280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5556635 RMVar_hsa_circ_60823,RMVar_hsa_circ_364476 85497 RMVar_ID_85497 Human_SNP_ID_499991773 m1A Human chr12 - 47079677 47079677 47079677 GAGGAACCCGGGAGAGCCCCCGGGAGCCAGCGAAGAGCTTGGCTGCTGCGTCCAGGGCTGCTGCT GAGGAACCCGGGAGAGCCCCCGGGAGCCAGCGGAGAGCTTGGCTGCTGCGTCCAGGGCTGCTGCT T C AMIGO2 Ensembl:ENSG00000139211 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47079639..47079704 26863196 MeRIP-seq:(Medium) rs1370037042 Functional Loss SNV dbSNP153 33..33 33 - - - 85498 RMVar_ID_85498 Human_SNP_ID_500150768 m1A Human chr12 - 47702811 47702811 47702811 ATAATGACTTCAGCAAATAAAGCAATCGAATTACAACTACAAGTGAAACAAAATGCAGAAGAATT ATAATGACTTCAGCAAATAAAGCAATCGAATTGCAACTACAAGTGAAACAAAATGCAGAAGAATT T C RPAP3 Ensembl:ENSG00000005175 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47702761..47702850 26863196 MeRIP-seq:(Medium) rs1316015105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246601,Human_RBP_ID_26906495,Human_RBP_ID_27805416 Human_Splice_Rec_1359254,Human_Splice_Rec_1359318,Human_Splice_Rec_1359354 RMVar_hsa_circ_350857,RMVar_hsa_circ_61937 85499 RMVar_ID_85499 Human_SNP_ID_500151582 m1A Human chr12 - 47705883 47705883 47705883 CGTAGGAGATCCTTGGGGTGGCCGGTGGGAGGAGGGGTAGCGGTTATGGGTACCGGTGAGGCGGG CGTAGGAGATCCTTGGGGTGGCCGGTGGGAGGGGGGGTAGCGGTTATGGGTACCGGTGAGGCGGG T C RPAP3 Ensembl:ENSG00000005175 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:47705832..47706007 26863196 MeRIP-seq:(Medium) rs1349417910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322472 85500 RMVar_ID_85500 Human_SNP_ID_500151583 m1A Human chr12 + 47705902 47705902 47705902 TAACCGCTACCCCTCCTCCCACCGGCCACCCCAAGGATCTCCTACGCTGCTCCGGGCAGCGAGAA TAACCGCTACCCCTCCTCCCACCGGCCACCCCGAGGATCTCCTACGCTGCTCCGGGCAGCGAGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47705899..47705985 26863196 MeRIP-seq:(Medium) rs1166871772 Functional Loss SNV dbSNP153 33..33 33 - - - 85501 RMVar_ID_85501 Human_SNP_ID_500162595 m1A Human chr12 + 47749118 47749118 47749118 CTTCCCTACCTTCCATGCATCCTGCCTCCCCCACAGCCTAGTCCCCCGCCCCCTGCATGCCCATC CTTCCCTACCTTCCATGCATCCTGCCTCCCCCCCAGCCTAGTCCCCCGCCCCCTGCATGCCCATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47749105..47749360 26863196 MeRIP-seq:(Medium) rs1436887005 Functional Loss SNV dbSNP153 33..33 33 - - - 85502 RMVar_ID_85502 Human_SNP_ID_500165264 m1A Human chr12 + 47759049 47759049 47759049 GGCAGGCTTTGGAGTCCGCACCCGGGGGTACCAGAGTGGACATCCGCCTGAGCCCAGAGTATCCC GGCAGGCTTTGGAGTCCGCACCCGGGGGTACCTGAGTGGACATCCGCCTGAGCCCAGAGTATCCC A T SLC48A1 Ensembl:ENSG00000211584 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:47759001..47759183;chr12:47758999..47759163 26863196 MeRIP-seq:(Medium) rs867512892 Functional Loss SNV dbSNP153 33..33 33 - - - 85503 RMVar_ID_85503 Human_SNP_ID_500168475 m1A Human chr12 - 47773306 47773306 47773306 CGCGGAGGCCGAGCTGCAGCCTGGACGGGGCCATGGGGCTGCGGCGCCGGGCGGGCCGAGGGCGA CGCGGAGGCCGAGCTGCAGCCTGGACGGGGCCCTGGGGCTGCGGCGCCGGGCGGGCCGAGGGCGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47773256..47773490 26863196 MeRIP-seq:(Medium) rs1486771895 Functional Loss SNV dbSNP153 33..33 33 - - - 85504 RMVar_ID_85504 Human_SNP_ID_500171137 m1A Human chr12 + 47783508 47783508 47783508 GTTTGCAGAGCCAGGAATAGTGGTTAAGGGTGAGCCCGACGGAGCCGGAGCCAGTCCTCCTCTGT GTTTGCAGAGCCAGGAATAGTGGTTAAGGGTGGGCCCGACGGAGCCGGAGCCAGTCCTCCTCTGT A G NONHSAG011023.2 RNACentral:URS00008B85A6 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47783460..47783675 26863196 MeRIP-seq:(Medium) rs1409046163 Functional Loss SNV dbSNP153 33..33 33 - - - 85505 RMVar_ID_85505 Human_SNP_ID_500171423 m1A Human chr12 - 47784465 47784462 47784466 TCAAAGGTGGCCTTGCAGCCACAGGGGATGAGAGAAAGGCTGGGCACCTGCTAGGACTCCCTCAC TCAAAGGTGGCCTTGCAGCCACAGGGGATGA____AAGGCTGGGCACCTGCTAGGACTCCCTCAC TTCTC T HDAC7 Ensembl:ENSG00000061273 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:47784459..47784560 32194978 MeRIP-seq:(Medium) rs1236087057 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_94527,RMVar_hsa_circ_122480,RMVar_hsa_circ_156144,RMVar_hsa_circ_156145 85506 RMVar_ID_85506 Human_SNP_ID_500174178 m1A Human chr12 + 47793453 47793453 47793453 GGCCTGGCTGGCAGGCTCTGGGGCTGACAGTGAGGCAGGTGCGGCTGGGGAAGACTGAGCCCGGG GGCCTGGCTGGCAGGCTCTGGGGCTGACAGTGGGGCAGGTGCGGCTGGGGAAGACTGAGCCCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47793403..47793529 26863196 MeRIP-seq:(Medium) rs1269535243 Functional Loss SNV dbSNP153 33..33 33 - - - 85507 RMVar_ID_85507 Human_SNP_ID_500175093 m1A Human chr12 - 47796288 47796288 47796288 TCCCTCTCTCCCCAACCCTCAGACTCCTCCCCAAGTAGTAGCAGCACGCCCGCATCAGGGTGCAG TCCCTCTCTCCCCAACCCTCAGACTCCTCCCCGAGTAGTAGCAGCACGCCCGCATCAGGGTGCAG T C HDAC7 Ensembl:ENSG00000061273 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:47796000..47796291 32194978 MeRIP-seq:(Medium) rs1249637464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1360044,Human_Splice_Rec_1360045,Human_Splice_Rec_1360092,Human_Splice_Rec_1360093,Human_Splice_Rec_1360182,Human_Splice_Rec_1360183,Human_Splice_Rec_1360252,Human_Splice_Rec_1360253,Human_Splice_Rec_1360298,Human_Splice_Rec_1360344,Human_Splice_Rec_1360345,Human_Splice_Rec_1360402,Human_Splice_Rec_1360403,Human_Splice_Rec_1360474,Human_Splice_Rec_1360475,Human_Splice_Rec_1360506,Human_Splice_Rec_1360507 Human_miRNA_ID_2367369,Human_miRNA_ID_3015166 RMVar_hsa_circ_94527,RMVar_hsa_circ_156145,RMVar_hsa_circ_362427,RMVar_hsa_circ_112146,RMVar_hsa_circ_24935,RMVar_hsa_circ_156147,RMVar_hsa_circ_156148,RMVar_hsa_circ_121539 85508 RMVar_ID_85508 Human_SNP_ID_500178380 m1A Human chr12 - 47808765 47808765 47808765 CCTAAGTGGGCAGAGCAGTGCAGGGGCAGGCCAGGCTATAAGCTGAAGGCCATGGGTAATAGGAA CCTAAGTGGGCAGAGCAGTGCAGGGGCAGGCCTGGCTATAAGCTGAAGGCCATGGGTAATAGGAA T A HDAC7 Ensembl:ENSG00000061273 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47808763..47809044 26863196 MeRIP-seq:(Medium) rs556992315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156148,RMVar_hsa_circ_121539 85509 RMVar_ID_85509 Human_SNP_ID_500179346 m1A Human chr12 + 47812864 47812864 47812864 TCTCTGGCGTCAGAATGGCACATTTCTTCCCTATTATCACACGATGCCCCTGGCTCACTCTCAAG TCTCTGGCGTCAGAATGGCACATTTCTTCCCTGTTATCACACGATGCCCCTGGCTCACTCTCAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:47812860..47813104 26863196 MeRIP-seq:(Medium) rs1396492284 Functional Loss SNV dbSNP153 33..33 33 - - - 85510 RMVar_ID_85510 Human_SNP_ID_500180754 m1A Human chr12 + 47818873 47818873 47818873 GCTGGGGAGGTCAGACCCAAACGGGCAGCCACAGCGGGAAGCAATGGGGGTGGGGCACTGGGTGG GCTGGGGAGGTCAGACCCAAACGGGCAGCCACGGCGGGAAGCAATGGGGGTGGGGCACTGGGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47818869..47819042 26863196 MeRIP-seq:(Medium) rs1416764622 Functional Loss SNV dbSNP153 33..33 33 - - - 85511 RMVar_ID_85511 Human_SNP_ID_500180755 m1A Human chr12 + 47818873 47818873 47818873 GCTGGGGAGGTCAGACCCAAACGGGCAGCCACAGCGGGAAGCAATGGGGGTGGGGCACTGGGTGG GCTGGGGAGGTCAGACCCAAACGGGCAGCCACTGCGGGAAGCAATGGGGGTGGGGCACTGGGTGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47818869..47819042 26863196 MeRIP-seq:(Medium) rs1416764622 Functional Loss SNV dbSNP153 33..33 33 - - - 85512 RMVar_ID_85512 Human_SNP_ID_500181055 m1A Human chr12 - 47819816 47819816 47819816 AGGCCGGCGCCCCAGCCCCCCGCCCCGCCATGAGCCCCCCGCTCTGAGGGCCCCGGCCCCTGGAT AGGCCGGCGCCCCAGCCCCCCGCCCCGCCATGGGCCCCCCGCTCTGAGGGCCCCGGCCCCTGGAT T C HDAC7 Ensembl:ENSG00000061273 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:47819712..47820000 26863196 MeRIP-seq:(Medium) rs1165940187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246609 Human_Splice_Rec_1360031,Human_Splice_Rec_1360079,Human_Splice_Rec_1360241,Human_Splice_Rec_1360483,Human_Splice_Rec_1360493,Human_Splice_Rec_1360519,Human_Splice_Rec_1360563,Human_Splice_Rec_1360573 RMVar_hsa_circ_156148,RMVar_hsa_circ_121539 85513 RMVar_ID_85513 Human_SNP_ID_500181056 m1A Human chr12 + 47819818 47819818 47819818 CCAGGGGCCGGGGCCCTCAGAGCGGGGGGCTCATGGCGGGGCGGGGGGCTGGGGCGCCGGCCTCA CCAGGGGCCGGGGCCCTCAGAGCGGGGGGCTCGTGGCGGGGCGGGGGGCTGGGGCGCCGGCCTCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:47819728..47819890 26863196 MeRIP-seq:(Medium) rs1565595693 Functional Loss SNV dbSNP153 33..33 33 - - - 85514 RMVar_ID_85514 Human_SNP_ID_500181077 m1A Human chr12 + 47819860 47819860 47819860 GGGGGGCTGGGGCGCCGGCCTCACATCCCCCCAGTCGCCGGAGGCTGCAGAGCGACTGTGAGACG GGGGGGCTGGGGCGCCGGCCTCACATCCCCCCTGTCGCCGGAGGCTGCAGAGCGACTGTGAGACG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:47819776..47819945;chr12:47819720..47819929 26863196 MeRIP-seq:(Medium) rs1441535243 Functional Loss SNV dbSNP153 33..33 33 - - - 85515 RMVar_ID_85515 Human_SNP_ID_500181098 m1A Human chr12 + 47819923 47819923 47819923 CGGCGAGAGGAAGGGAGGGGGCCGGGAGGGGGAGGGCCCTGGCAGCCCGGCCGGCCGGGTAGGAT CGGCGAGAGGAAGGGAGGGGGCCGGGAGGGGGGGGGCCCTGGCAGCCCGGCCGGCCGGGTAGGAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:47819876..47819925 26863196 MeRIP-seq:(Medium) rs1234764435 Functional Loss SNV dbSNP153 33..33 33 - - - 85516 RMVar_ID_85516 Human_SNP_ID_500187269 m1A Human chr12 - 47844900 47844897 47844900 CATCCGCTGCCGCCACCCGCCCCCGGGCAGCCACCTGCTCTATGCCAAGATGATCCAGAAGCTAG CATCCGCTGCCGCCACCCGCCCCCGGGCAGCC___TGCTCTATGCCAAGATGATCCAGAAGCTAG AGGT A VDR Ensembl:ENSG00000111424 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:47844852..47844971 26863196 MeRIP-seq:(Medium) rs1198279499 Functional Loss DEL dbSNP153 33..35 33 - - - 85517 RMVar_ID_85517 Human_SNP_ID_500202303 m1A Human chr12 - 47902867 47902867 47902867 CAGGTGTCCAAAGCCCAGGCTGTGAATGGAGAAAGGCCTGGGACCGAGTGGGCTACATCAGGTGG CAGGTGTCCAAAGCCCAGGCTGTGAATGGAGACAGGCCTGGGACCGAGTGGGCTACATCAGGTGG T G VDR Ensembl:ENSG00000111424 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:47902818..47902963 26863196 MeRIP-seq:(Medium) rs147955028 Functional Loss SNV dbSNP153 33..33 33 - - - 85518 RMVar_ID_85518 Human_SNP_ID_500202873 m1A Human chr12 + 47904977 47904977 47904977 GGGTTCGCACCTGGTCCGGCCGGCGGGTGGACAAGCTGTTCCGCGCTCCCGGCGCACACGGCTCC GGGTTCGCACCTGGTCCGGCCGGCGGGTGGACCAGCTGTTCCGCGCTCCCGGCGCACACGGCTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:47904842..47904985 26863196 MeRIP-seq:(Medium) rs947511815 Functional Loss SNV dbSNP153 33..33 33 - - - 85519 RMVar_ID_85519 Human_SNP_ID_500202874 m1A Human chr12 - 47904981 47904981 47904981 CAGCGGAGCCGTGTGCGCCGGGAGCGCGGAACAGCTTGTCCACCCGCCGGCCGGACCAGGTGCGA CAGCGGAGCCGTGTGCGCCGGGAGCGCGGAACGGCTTGTCCACCCGCCGGCCGGACCAGGTGCGA T C VDR Ensembl:ENSG00000111424 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47904780..47904982 26863196 MeRIP-seq:(Medium) rs1043299018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1360601,Human_Splice_Rec_1360669,Human_Splice_Rec_1360685,Human_Splice_Rec_1360703 85520 RMVar_ID_85520 Human_SNP_ID_500216593 m1A Human chr12 + 47964226 47964226 47964226 CTCTTTTCATCTTAGGACATGACACCAGTGGCATATCACGGCCATGGGGTCTCAGCATTCCGCTG CTCTTTTCATCTTAGGACATGACACCAGTGGCGTATCACGGCCATGGGGTCTCAGCATTCCGCTG A G TMEM106C Ensembl:ENSG00000134291 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:47963601..47964354 26863196 MeRIP-seq:(Medium) rs774564180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228923,Human_RBP_ID_420102,Human_RBP_ID_4223049,Human_RBP_ID_8376513,Human_RBP_ID_22493248,Human_RBP_ID_26906500 Human_Splice_Rec_1360720,Human_Splice_Rec_1360732,Human_Splice_Rec_1360742,Human_Splice_Rec_1360756,Human_Splice_Rec_1360760,Human_Splice_Rec_1360764,Human_Splice_Rec_1360778,Human_Splice_Rec_1360780,Human_Splice_Rec_1360804,Human_Splice_Rec_1360814,Human_Splice_Rec_1360828,Human_Splice_Rec_1360838,Human_Splice_Rec_1360852,Human_Splice_Rec_1360856 RMVar_hsa_circ_116629,RMVar_hsa_circ_46674,RMVar_hsa_circ_156157 85521 RMVar_ID_85521 Human_SNP_ID_500216616 m1A Human chr12 + 47964286 47964286 47964286 CGCTGCTGCTCGCCCCTCCTCCTGCAGGCGAAAGCAAGAAGATGACAGGGACGGTTTGCTGGCTG CGCTGCTGCTCGCCCCTCCTCCTGCAGGCGAACGCAAGAAGATGACAGGGACGGTTTGCTGGCTG A C TMEM106C Ensembl:ENSG00000134291 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:47964201..47964493 32194978 MeRIP-seq:(Medium) rs200250774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1795541,Human_RBP_ID_4246612,Human_RBP_ID_5555252,Human_RBP_ID_18976971,Human_RBP_ID_22436987 Human_Splice_Rec_1360720,Human_Splice_Rec_1360732,Human_Splice_Rec_1360742,Human_Splice_Rec_1360760,Human_Splice_Rec_1360764,Human_Splice_Rec_1360778,Human_Splice_Rec_1360780,Human_Splice_Rec_1360794,Human_Splice_Rec_1360804,Human_Splice_Rec_1360814,Human_Splice_Rec_1360828,Human_Splice_Rec_1360838,Human_Splice_Rec_1360852,Human_Splice_Rec_1360856 Human_miRNA_ID_2444145 RMVar_hsa_circ_116629,RMVar_hsa_circ_46674,RMVar_hsa_circ_156157 85522 RMVar_ID_85522 Human_SNP_ID_500216622 m1A Human chr12 - 47964296 47964296 47964296 TGCTCTCGTTCAGCCAGCAAACCGTCCCTGTCATCTTCTTGCTTTCGCCTGCAGGAGGAGGGGCG TGCTCTCGTTCAGCCAGCAAACCGTCCCTGTCGTCTTCTTGCTTTCGCCTGCAGGAGGAGGGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47964201..47964446 26863196 MeRIP-seq:(Medium) rs746440188 Functional Loss SNV dbSNP153 33..33 33 - - - 85523 RMVar_ID_85523 Human_SNP_ID_500216631 m1A Human chr12 + 47964323 47964323 47964323 GAAGATGACAGGGACGGTTTGCTGGCTGAACGAGAGCAGGAAGAAGCCATTGCTCAGTTCCCATA GAAGATGACAGGGACGGTTTGCTGGCTGAACGGGAGCAGGAAGAAGCCATTGCTCAGTTCCCATA A G TMEM106C Ensembl:ENSG00000134291 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47964201..47964370 26863196 MeRIP-seq:(Medium) rs1247427445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420106,Human_RBP_ID_876630,Human_RBP_ID_1472076,Human_RBP_ID_1795541,Human_RBP_ID_4246612,Human_RBP_ID_6188502,Human_RBP_ID_8376514,Human_RBP_ID_8940705,Human_RBP_ID_9017487,Human_RBP_ID_11949324,Human_RBP_ID_18434208,Human_RBP_ID_18976971,Human_RBP_ID_22436987,Human_RBP_ID_23560741 Human_Splice_Rec_1360794 RMVar_hsa_circ_116629,RMVar_hsa_circ_156157 85524 RMVar_ID_85524 Human_SNP_ID_500216632 m1A Human chr12 + 47964325 47964325 47964325 AGATGACAGGGACGGTTTGCTGGCTGAACGAGAGCAGGAAGAAGCCATTGCTCAGTTCCCATATG AGATGACAGGGACGGTTTGCTGGCTGAACGAGTGCAGGAAGAAGCCATTGCTCAGTTCCCATATG A T TMEM106C Ensembl:ENSG00000134291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:47964201..47964375 26863196 MeRIP-seq:(Medium) rs1447751142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420106,Human_RBP_ID_876630,Human_RBP_ID_1472076,Human_RBP_ID_1795541,Human_RBP_ID_4246612,Human_RBP_ID_6188502,Human_RBP_ID_8376514,Human_RBP_ID_8940705,Human_RBP_ID_9017487,Human_RBP_ID_11949324,Human_RBP_ID_18434208,Human_RBP_ID_18976971,Human_RBP_ID_22436987,Human_RBP_ID_23560741 Human_Splice_Rec_1360721,Human_Splice_Rec_1360733,Human_Splice_Rec_1360743,Human_Splice_Rec_1360757,Human_Splice_Rec_1360761,Human_Splice_Rec_1360765,Human_Splice_Rec_1360781,Human_Splice_Rec_1360794,Human_Splice_Rec_1360795,Human_Splice_Rec_1360815,Human_Splice_Rec_1360829,Human_Splice_Rec_1360839,Human_Splice_Rec_1360853,Human_Splice_Rec_1360871,Human_Splice_Rec_1360879 RMVar_hsa_circ_116629,RMVar_hsa_circ_156157 85525 RMVar_ID_85525 Human_SNP_ID_500217295 m1A Human chr12 - 47966734 47966734 47966734 TAGAGAGCACACACAGAGAGAACAGTGTCCTTACTACACATAGGAAAACGGTCCTCCCATCTCGG TAGAGAGCACACACAGAGAGAACAGTGTCCTTGCTACACATAGGAAAACGGTCCTCCCATCTCGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:47966676..47966801 32194978 MeRIP-seq:(Medium) rs775737747 Functional Loss SNV dbSNP153 33..33 33 - - - 85526 RMVar_ID_85526 Human_SNP_ID_500217438 m1A Human chr12 - 47967210 47967207 47967210 TGTGCACCAGGATCTCAGGTACCGTGCAGAAGAAGCTACCAAACAGCAAATATGGAAATAGTCAG TGTGCACCAGGATCTCAGGTACCGTGCAGAAG___CTACCAAACAGCAAATATGGAAATAGTCAG GCTT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:47967201..47967275 32194978 MeRIP-seq:(Medium) rs1444174424 Functional Loss DEL dbSNP153 33..35 33 - - - 85527 RMVar_ID_85527 Human_SNP_ID_500217439 m1A Human chr12 - 47967210 47967210 47967210 TGTGCACCAGGATCTCAGGTACCGTGCAGAAGAAGCTACCAAACAGCAAATATGGAAATAGTCAG TGTGCACCAGGATCTCAGGTACCGTGCAGAAGGAGCTACCAAACAGCAAATATGGAAATAGTCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:47967201..47967275 32194978 MeRIP-seq:(Medium) rs200676671 Functional Loss SNV dbSNP153 33..33 33 - - - 85528 RMVar_ID_85528 Human_SNP_ID_500217440 m1A Human chr12 - 47967210 47967210 47967210 TGTGCACCAGGATCTCAGGTACCGTGCAGAAGAAGCTACCAAACAGCAAATATGGAAATAGTCAG TGTGCACCAGGATCTCAGGTACCGTGCAGAAGCAGCTACCAAACAGCAAATATGGAAATAGTCAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:47967201..47967275 32194978 MeRIP-seq:(Medium) rs200676671 Functional Loss SNV dbSNP153 33..33 33 - - - 85529 RMVar_ID_85529 Human_SNP_ID_500252963 m1A Human chr12 + 48105953 48105953 48105953 CCGCTTCCGCCCAGTCCAGCCCGGGCCGGCTGACCGGGTCCGACACAGTCTCCTGGACCAGGCTC CCGCTTCCGCCCAGTCCAGCCCGGGCCGGCTGTCCGGGTCCGACACAGTCTCCTGGACCAGGCTC A T PFKM Ensembl:ENSG00000152556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48105906..48105994 26863196 MeRIP-seq:(Medium) rs1393750362 Functional Loss SNV dbSNP153 33..33 33 - - - 85530 RMVar_ID_85530 Human_SNP_ID_500254446 m1A Human chr12 + 48111757 48111757 48111757 GTGAATATCGGGTGGATCAAAGAGAGACAGTCATGGGGGTCAGGTGTGGTATCCAGAATAATGTG GTGAATATCGGGTGGATCAAAGAGAGACAGTCTTGGGGGTCAGGTGTGGTATCCAGAATAATGTG A T PFKM Ensembl:ENSG00000152556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48111751..48111858 26863196 MeRIP-seq:(Medium) rs1187679960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35316,RMVar_hsa_circ_60413 85531 RMVar_ID_85531 Human_SNP_ID_500256342 m1A Human chr12 + 48119405 48119405 48119405 GAAAGCAGCGGCGGAGGAGAGCTAAGACTAAAAGGCAAGAGGGGCCATTGAGTGAAGAGCAAGGG GAAAGCAGCGGCGGAGGAGAGCTAAGACTAAAGGGCAAGAGGGGCCATTGAGTGAAGAGCAAGGG A G PFKM Ensembl:ENSG00000152556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:48119351..48119565;chr12:48119393..48119497 26863196 MeRIP-seq:(Medium) rs1264087047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1361763 RMVar_hsa_circ_35316,RMVar_hsa_circ_60413 85532 RMVar_ID_85532 Human_SNP_ID_500257057 m1A Human chr12 - 48122756 48122756 48122756 TCTTCATGGGTCATGATCCACTCTAGAATTTAAGACAATGGTCAGTTAAGACACAGCAGGAATCA TCTTCATGGGTCATGATCCACTCTAGAATTTAGGACAATGGTCAGTTAAGACACAGCAGGAATCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48122751..48122825 26863196 MeRIP-seq:(Medium) rs781022441 Functional Loss SNV dbSNP153 33..33 33 - - - 85533 RMVar_ID_85533 Human_SNP_ID_500259650 m1A Human chr12 + 48133401 48133401 48133401 TGGTTGGGTCAATTGACAATGACTTCTGTGGCACCGATATGACCATTGGCACTGACTCTGCCCTG TGGTTGGGTCAATTGACAATGACTTCTGTGGCGCCGATATGACCATTGGCACTGACTCTGCCCTG A G PFKM Ensembl:ENSG00000152556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48133351..48133435 26863196 MeRIP-seq:(Medium) rs139800248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116526,Human_RBP_ID_1472126,Human_RBP_ID_11950083 Human_Splice_Rec_1361434,Human_Splice_Rec_1361435,Human_Splice_Rec_1361486,Human_Splice_Rec_1361487,Human_Splice_Rec_1361530,Human_Splice_Rec_1361531,Human_Splice_Rec_1361582,Human_Splice_Rec_1361583,Human_Splice_Rec_1361634,Human_Splice_Rec_1361635,Human_Splice_Rec_1361702,Human_Splice_Rec_1361703,Human_Splice_Rec_1361772,Human_Splice_Rec_1361773,Human_Splice_Rec_1361820,Human_Splice_Rec_1361821,Human_Splice_Rec_1361882,Human_Splice_Rec_1361890,Human_Splice_Rec_1361891,Human_Splice_Rec_1361942,Human_Splice_Rec_1361943,Human_Splice_Rec_1361984,Human_Splice_Rec_1361992,Human_Splice_Rec_1361993,Human_Splice_Rec_1362036,Human_Splice_Rec_1362037 RMVar_hsa_circ_35628,RMVar_hsa_circ_60413,RMVar_hsa_circ_31436 85534 RMVar_ID_85534 Human_SNP_ID_500260038 m1A Human chr12 - 48134814 48134814 48134814 AAATAAAGTGCAAGTACCTCGCTGAGTCGGCGACAAAGGTGTTCCTCCCAGTCGTCATCTGGTGG AAATAAAGTGCAAGTACCTCGCTGAGTCGGCGGCAAAGGTGTTCCTCCCAGTCGTCATCTGGTGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48133471..48134816 32194978 MeRIP-seq:(Medium) rs1406800853 Functional Loss SNV dbSNP153 33..33 33 - - - 85535 RMVar_ID_85535 Human_SNP_ID_500260085 m1A Human chr12 - 48134965 48134965 48134965 CAATTGCACCCTCAGCCACAATGATGATGTTGAGACGAGAACCACGGGTCCTTGTCTGGTTGAGA CAATTGCACCCTCAGCCACAATGATGATGTTGCGACGAGAACCACGGGTCCTTGTCTGGTTGAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48134951..48135000 32194978 MeRIP-seq:(Medium) rs1565891441 Functional Loss SNV dbSNP153 33..33 33 - - - 85536 RMVar_ID_85536 Human_SNP_ID_500260817 m1A Human chr12 + 48137775 48137775 48137775 CAGTGATGGCACTTTTGGAGGGGACCCCAGATACCCCAGCCTGTGTAGTGAGCCTCTCTGGTAAC CAGTGATGGCACTTTTGGAGGGGACCCCAGATCCCCCAGCCTGTGTAGTGAGCCTCTCTGGTAAC A C PFKM Ensembl:ENSG00000152556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48137679..48137885 26863196 MeRIP-seq:(Medium) rs753592471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3276 Human_Splice_Rec_1361444,Human_Splice_Rec_1361445,Human_Splice_Rec_1361496,Human_Splice_Rec_1361497,Human_Splice_Rec_1361538,Human_Splice_Rec_1361539,Human_Splice_Rec_1361592,Human_Splice_Rec_1361593,Human_Splice_Rec_1361642,Human_Splice_Rec_1361643,Human_Splice_Rec_1361712,Human_Splice_Rec_1361713,Human_Splice_Rec_1361782,Human_Splice_Rec_1361783,Human_Splice_Rec_1361828,Human_Splice_Rec_1361829,Human_Splice_Rec_1361866,Human_Splice_Rec_1361900,Human_Splice_Rec_1361901,Human_Splice_Rec_1361950,Human_Splice_Rec_1361951,Human_Splice_Rec_1362002,Human_Splice_Rec_1362003,Human_Splice_Rec_1362046,Human_Splice_Rec_1362047,Human_Splice_Rec_1362081,Human_Splice_Rec_1362089 Human_miRNA_ID_1356316 RMVar_hsa_circ_60413,RMVar_hsa_circ_31436,RMVar_hsa_circ_276685 85537 RMVar_ID_85537 Human_SNP_ID_500263313 m1A Human chr12 - 48148285 48148285 48148285 TCTCTTCCTGAGAAACAGTGTGTTCTAATGGGATTCCCAGGCAGTTCCTACACCTACGGTGTGTG TCTCTTCCTGAGAAACAGTGTGTTCTAATGGGCTTCCCAGGCAGTTCCTACACCTACGGTGTGTG T G ASB8 Ensembl:ENSG00000177981 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48148235..48148336 32194978 MeRIP-seq:(Medium) rs74089125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6188812,Human_RBP_ID_8376620,Human_RBP_ID_17471381,Human_RBP_ID_17684506,Human_RBP_ID_22493259 85538 RMVar_ID_85538 Human_SNP_ID_500263692 m1A Human chr12 - 48149679 48149679 48149679 CGCAGAGGTCAGAGTCATCAACCTAATAGGCCAGACACCCATCTCCCGCCTGGTGGCTCTGCTAG CGCAGAGGTCAGAGTCATCAACCTAATAGGCCGGACACCCATCTCCCGCCTGGTGGCTCTGCTAG T C ASB8 Ensembl:ENSG00000177981 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48149631..48150030 32194978 MeRIP-seq:(Medium) rs1459007961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4223362,Human_RBP_ID_6188826 85539 RMVar_ID_85539 Human_SNP_ID_500264653 m1A Human chr12 - 48153468 48153468 48153468 CTTGATGAGTTCCAGTATGTGGTATATTATGCAGAGCATTCAGAGCAAATACTCTCTCTCCGAGC CTTGATGAGTTCCAGTATGTGGTATATTATGCGGAGCATTCAGAGCAAATACTCTCTCTCCGAGC T C ASB8 Ensembl:ENSG00000177981 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48153419..48153526 26863196 MeRIP-seq:(Medium) rs188638799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1362118,Human_Splice_Rec_1362124,Human_Splice_Rec_1362134,Human_Splice_Rec_1362142,Human_Splice_Rec_1362148,Human_Splice_Rec_1362156,Human_Splice_Rec_1362164,Human_Splice_Rec_1362174,Human_Splice_Rec_1362180,Human_Splice_Rec_1362190,Human_Splice_Rec_1362198,Human_Splice_Rec_1362204,Human_Splice_Rec_1362212,Human_Splice_Rec_1362216,Human_Splice_Rec_1362222 Human_miRNA_ID_2395544,Human_miRNA_ID_2907810,Human_miRNA_ID_3026648 RMVar_hsa_circ_1020,RMVar_hsa_circ_30855,RMVar_hsa_circ_72518,RMVar_hsa_circ_86553,RMVar_hsa_circ_358749,RMVar_hsa_circ_156182 85540 RMVar_ID_85540 Human_SNP_ID_500264659 m1A Human chr12 - 48153487 48153487 48153487 GCATGTGAACACCTTGAGCCTTGATGAGTTCCAGTATGTGGTATATTATGCAGAGCATTCAGAGC GCATGTGAACACCTTGAGCCTTGATGAGTTCCTGTATGTGGTATATTATGCAGAGCATTCAGAGC T A ASB8 Ensembl:ENSG00000177981 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48153436..48153511 26863196 MeRIP-seq:(Medium) rs199904430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1472135,Human_RBP_ID_1795653,Human_RBP_ID_3406585,Human_RBP_ID_11950395 Human_Splice_Rec_1362118,Human_Splice_Rec_1362124,Human_Splice_Rec_1362134,Human_Splice_Rec_1362142,Human_Splice_Rec_1362148,Human_Splice_Rec_1362156,Human_Splice_Rec_1362164,Human_Splice_Rec_1362174,Human_Splice_Rec_1362180,Human_Splice_Rec_1362190,Human_Splice_Rec_1362198,Human_Splice_Rec_1362204,Human_Splice_Rec_1362212,Human_Splice_Rec_1362216,Human_Splice_Rec_1362222 RMVar_hsa_circ_1020,RMVar_hsa_circ_30855,RMVar_hsa_circ_72518,RMVar_hsa_circ_86553,RMVar_hsa_circ_358749,RMVar_hsa_circ_156182 85541 RMVar_ID_85541 Human_SNP_ID_500388567 m1A Human chr12 - 48654138 48654138 48654138 GATGCAGATGGCTGGAGATGGGTGCAGATCCCAGGGATCTCGAAATTCTGAGAAAGCCTCTGCAC GATGCAGATGGCTGGAGATGGGTGCAGATCCCGGGGATCTCGAAATTCTGAGAAAGCCTCTGCAC T C KANSL2 Ensembl:ENSG00000139620 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48653848..48654148 32194978 MeRIP-seq:(Medium) rs1218468459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420294,Human_RBP_ID_1472157,Human_RBP_ID_4223431,Human_RBP_ID_6189121,Human_RBP_ID_11950911,Human_RBP_ID_17819956 Human_Splice_Rec_1362470 RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 85542 RMVar_ID_85542 Human_SNP_ID_500419058 m1A Human chr12 - 48766524 48766524 48766524 CCAGCCATATCCCTGGATAGGAAGGGATAGGAAGAGACTACTTGGTGCCATGGGGTAGGGGTGAG CCAGCCATATCCCTGGATAGGAAGGGATAGGAGGAGACTACTTGGTGCCATGGGGTAGGGGTGAG T C ADCY6 Ensembl:ENSG00000174233 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:48766376..48766575 26863196 MeRIP-seq:(Medium) rs1339751320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6189715,Human_RBP_ID_8068280 Human_miRNA_ID_1188543 85543 RMVar_ID_85543 Human_SNP_ID_500419450 m1A Human chr12 + 48768483 48768483 48768483 CACAGCCTGCTGGGATGTTCCCTTTTGTGGTTAGCAGGGTCTGGAGGCTCAGTGCCCCCTGCCAC CACAGCCTGCTGGGATGTTCCCTTTTGTGGTTGGCAGGGTCTGGAGGCTCAGTGCCCCCTGCCAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48768432..48768952 32194978 MeRIP-seq:(Medium) rs1359155723 Functional Loss SNV dbSNP153 33..33 33 - - - 85544 RMVar_ID_85544 Human_SNP_ID_500421232 m1A Human chr12 + 48774538 48774538 48774538 CCTTAGGGAACAGCTAGAGGCATCAAGAGACCAAGAGTTGAAGGTTGTATCAGCCAAGGAGGAAT CCTTAGGGAACAGCTAGAGGCATCAAGAGACCGAGAGTTGAAGGTTGTATCAGCCAAGGAGGAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48774536..48774647 26863196 MeRIP-seq:(Medium) rs777525532 Functional Loss SNV dbSNP153 33..33 33 - - - 85545 RMVar_ID_85545 Human_SNP_ID_500422302 m1A Human chr12 - 48777735 48777735 48777735 TAGTGATGCCCTATTGGAACCACTGGGCTAGGAGCGGCTGCTGCTGTCGGTATTGCCCCAGCACG TAGTGATGCCCTATTGGAACCACTGGGCTAGGGGCGGCTGCTGCTGTCGGTATTGCCCCAGCACG T C ADCY6 Ensembl:ENSG00000174233 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48777653..48778274 32194978 MeRIP-seq:(Medium) rs1029439794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1362588,Human_Splice_Rec_1362628,Human_Splice_Rec_1362666,Human_Splice_Rec_1362736,Human_Splice_Rec_1362744 RMVar_hsa_circ_357853,RMVar_hsa_circ_377964,RMVar_hsa_circ_115446,RMVar_hsa_circ_156219 85546 RMVar_ID_85546 Human_SNP_ID_500423390 m1A Human chr12 - 48782388 48782388 48782388 GGTGGGAGGCTAGGGTTGAGGGGTCTGCCTCCATGTGGGATCTGGGGTAGAGGACACTGCTGAGG GGTGGGAGGCTAGGGTTGAGGGGTCTGCCTCCGTGTGGGATCTGGGGTAGAGGACACTGCTGAGG T C ADCY6 Ensembl:ENSG00000174233 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:48782381..48782480 26863196 MeRIP-seq:(Medium) rs1280721430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418932,Human_RBP_ID_5348248,Human_RBP_ID_8177350,Human_RBP_ID_17186533,Human_RBP_ID_18934399,Human_RBP_ID_19056071 RMVar_hsa_circ_357853,RMVar_hsa_circ_377964,RMVar_hsa_circ_115446,RMVar_hsa_circ_78936,RMVar_hsa_circ_156219,RMVar_hsa_circ_156220 85547 RMVar_ID_85547 Human_SNP_ID_500423391 m1A Human chr12 - 48782388 48782388 48782388 GGTGGGAGGCTAGGGTTGAGGGGTCTGCCTCCATGTGGGATCTGGGGTAGAGGACACTGCTGAGG GGTGGGAGGCTAGGGTTGAGGGGTCTGCCTCCCTGTGGGATCTGGGGTAGAGGACACTGCTGAGG T G ADCY6 Ensembl:ENSG00000174233 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:48782381..48782480 26863196 MeRIP-seq:(Medium) rs1280721430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418932,Human_RBP_ID_5348248,Human_RBP_ID_8177350,Human_RBP_ID_17186533,Human_RBP_ID_18934399,Human_RBP_ID_19056071 RMVar_hsa_circ_357853,RMVar_hsa_circ_377964,RMVar_hsa_circ_115446,RMVar_hsa_circ_78936,RMVar_hsa_circ_156219,RMVar_hsa_circ_156220 85548 RMVar_ID_85548 Human_SNP_ID_500423512 m1A Human chr12 + 48782729 48782729 48782729 GACAAAGAACACAGGGCACCAGAGGCCCGCAGAGGGGCTGCGCGGGTCTGCTGCGAGAGCGCCCC GACAAAGAACACAGGGCACCAGAGGCCCGCAGGGGGGCTGCGCGGGTCTGCTGCGAGAGCGCCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48782679..48782791 26863196 MeRIP-seq:(Medium) rs756705285 Functional Loss SNV dbSNP153 33..33 33 - - - 85549 RMVar_ID_85549 Human_SNP_ID_500424823 m1A Human chr12 + 48787653 48787653 48787653 TTGTCCAGCAACCCATCACTATGAGCCCTGGGAGCACAGACCACCTCCCTCCTCCCCAGAGTCAG TTGTCCAGCAACCCATCACTATGAGCCCTGGGGGCACAGACCACCTCCCTCCTCCCCAGAGTCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:48787645..48787784 26863196 MeRIP-seq:(Medium) rs888578742 Functional Loss SNV dbSNP153 33..33 33 - - - 85550 RMVar_ID_85550 Human_SNP_ID_500425145 m1A Human chr12 - 48788961 48788961 48788961 GAGGACCGCGGGACGGCCGGCCGGCCGGCCGGAGCCCGCGGGGGCGGCGGGGCGGGGGCCCAGGG GAGGACCGCGGGACGGCCGGCCGGCCGGCCGGGGCCCGCGGGGGCGGCGGGGCGGGGGCCCAGGG T C ADCY6 Ensembl:ENSG00000174233 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:48788805..48789100 26863196 MeRIP-seq:(Medium) rs1565654033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229272,Human_RBP_ID_4246069,Human_RBP_ID_18934408,Human_RBP_ID_26777283 Human_Splice_Rec_1362623 RMVar_hsa_circ_78936,RMVar_hsa_circ_156220 85551 RMVar_ID_85551 Human_SNP_ID_500425165 m1A Human chr12 - 48789009 48789009 48789009 ACGGCGGACGGCGGACGGCGGGCGGGACGGCCAGGACGCGCGGGCTCGGAGGACCGCGGGACGGC ACGGCGGACGGCGGACGGCGGGCGGGACGGCCGGGACGCGCGGGCTCGGAGGACCGCGGGACGGC T C ADCY6 Ensembl:ENSG00000174233 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:48788597..48789087;chr12:48788832..48789075;chr12:48788555..48789120;chr12:48788527..48789134;chr12:48788605..48789110 26863196 MeRIP-seq:(Medium) rs1484718184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810397,Human_RBP_ID_3418943,Human_RBP_ID_4246070,Human_RBP_ID_8177358,Human_RBP_ID_26777283 Human_miRNA_ID_2937473 RMVar_hsa_circ_78936,RMVar_hsa_circ_156220 85552 RMVar_ID_85552 Human_SNP_ID_500425177 m1A Human chr12 - 48789027 48789027 48789027 GGGGCGAGGGCCGGGCGGACGGCGGACGGCGGACGGCGGGCGGGACGGCCAGGACGCGCGGGCTC GGGGCGAGGGCCGGGCGGACGGCGGACGGCGGGCGGCGGGCGGGACGGCCAGGACGCGCGGGCTC T C ADCY6 Ensembl:ENSG00000174233 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:48788751..48789075 26863196 MeRIP-seq:(Medium) rs1021913427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246070 RMVar_hsa_circ_78936,RMVar_hsa_circ_156220 85553 RMVar_ID_85553 Human_SNP_ID_500431617 m1A Human chr12 + 48814954 48814953 48814954 GAGCTGAGACCCGCTGCACCAGAACCCAGGAGAGGGGGGAGACGGCAGAGACTCCGCGGGCGCGG GAGCTGAGACCCGCTGCACCAGAACCCAGGAG_GGGGGGAGACGGCAGAGACTCCGCGGGCGCGG GA G CACNB3 Ensembl:ENSG00000167535 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:48814917..48815007 26863196 MeRIP-seq:(Medium) rs772562279 Functional Loss DEL dbSNP153 33..33 33 - - - 85554 RMVar_ID_85554 Human_SNP_ID_500431762 m1A Human chr12 - 48815437 48815437 48815437 GTCAGTCTCTGGCTCTCCCTGCCTTTCAGCCCAGCCTCTCTCCACTTCCGTCTCTCCTGTCTAAG GTCAGTCTCTGGCTCTCCCTGCCTTTCAGCCCTGCCTCTCTCCACTTCCGTCTCTCCTGTCTAAG T A lnc-BBS5-6,lnc-ADCY6-1 RNACentral:URS0000E2127A,RNACentral:URS0000D56CD6 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:48815246..48815476 26863196 MeRIP-seq:(Medium) rs867980925 Functional Loss SNV dbSNP153 33..33 33 - - - 85555 RMVar_ID_85555 Human_SNP_ID_500432494 m1A Human chr12 - 48818412 48818412 48818412 AGAGATGCGGAGACAGAGACGCTCGGCAACCCAGGAACTACTCCGCCGGGAAACAAAGGGCTGCG AGAGATGCGGAGACAGAGACGCTCGGCAACCCTGGAACTACTCCGCCGGGAAACAAAGGGCTGCG T A lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48818411..48818598 26863196 MeRIP-seq:(Medium) rs1163174832 Functional Loss SNV dbSNP153 33..33 33 - - - 85556 RMVar_ID_85556 Human_SNP_ID_500432651 m1A Human chr12 - 48818770 48818770 48818770 GCGAGAGAGCGCGAAGGAGGGAGCGAGCCGCGAAGACCAGCTGCTCGGAGCTCAGATCACCGCTC GCGAGAGAGCGCGAAGGAGGGAGCGAGCCGCGTAGACCAGCTGCTCGGAGCTCAGATCACCGCTC T A lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48818768..48818919 26863196 MeRIP-seq:(Medium) rs1016172450 Functional Loss SNV dbSNP153 33..33 33 - - - 85557 RMVar_ID_85557 Human_SNP_ID_500432652 m1A Human chr12 - 48818770 48818770 48818770 GCGAGAGAGCGCGAAGGAGGGAGCGAGCCGCGAAGACCAGCTGCTCGGAGCTCAGATCACCGCTC GCGAGAGAGCGCGAAGGAGGGAGCGAGCCGCGGAGACCAGCTGCTCGGAGCTCAGATCACCGCTC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48818768..48818919 26863196 MeRIP-seq:(Medium) rs1016172450 Functional Loss SNV dbSNP153 33..33 33 - - - 85558 RMVar_ID_85558 Human_SNP_ID_500437732 m1A Human chr12 + 48838001 48838001 48838001 ACTGTTTCCTTTTCTTCCTCTCTTCTTCAAGCATCCTCTGCCGCTCTTCCACCTCCTGCTGCCGT ACTGTTTCCTTTTCTTCCTCTCTTCTTCAAGCGTCCTCTGCCGCTCTTCCACCTCCTGCTGCCGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:48837892..48838100;chr12:48837876..48838050;chr12:48837888..48838099 26863196 MeRIP-seq:(Medium) rs375814765 Functional Loss SNV dbSNP153 33..33 33 - - - 85559 RMVar_ID_85559 Human_SNP_ID_500437761 m1A Human chr12 - 48838065 48838065 48838065 TCCAATCTCTTTTGTAGCCCAAGTTCCTCTCTAAAGCAGAACGAGAGGCTGAAGCTCTAAAGCGA TCCAATCTCTTTTGTAGCCCAAGTTCCTCTCTCAAGCAGAACGAGAGGCTGAAGCTCTAAAGCGA T G DDX23 Ensembl:ENSG00000174243 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48837969..48838070 32194978 MeRIP-seq:(Medium) rs758437451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35499,Human_RBP_ID_878034,Human_RBP_ID_9364875,Human_RBP_ID_18977045,Human_RBP_ID_22644737,Human_RBP_ID_26321379,Human_RBP_ID_27806597 Human_Splice_Rec_1363066,Human_Splice_Rec_1363090,Human_Splice_Rec_1363132,Human_Splice_Rec_1363162,Human_Splice_Rec_1363174,Human_Splice_Rec_1363186 RMVar_hsa_circ_156227,RMVar_hsa_circ_96672,RMVar_hsa_circ_60951 85560 RMVar_ID_85560 Human_SNP_ID_500440298 m1A Human chr12 + 48845630 48845630 48845630 CGAGAGCGAGAACGGCTGCCTCCTCGACGTCTATCCCTTGAACGATGCCGCTTTCTATCTTTAGA CGAGAGCGAGAACGGCTGCCTCCTCGACGTCTGTCCCTTGAACGATGCCGCTTTCTATCTTTAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48839866..48845629 32194978 MeRIP-seq:(Medium) rs757833729 Functional Loss SNV dbSNP153 33..33 33 - - - 85561 RMVar_ID_85561 Human_SNP_ID_500440328 m1A Human chr12 - 48845714 48845714 48845714 GCATCACCTTCCAAGGAGGAAAGGAAGCGATCACGGACTCCTGACAGAGAGCGGGATAGAGACCG GCATCACCTTCCAAGGAGGAAAGGAAGCGATCGCGGACTCCTGACAGAGAGCGGGATAGAGACCG T C DDX23 Ensembl:ENSG00000174243 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48840118..48845800 32194978 MeRIP-seq:(Medium) rs763554389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4255208,Human_RBP_ID_6189778,Human_RBP_ID_8781864,Human_RBP_ID_26321389 Human_Splice_Rec_1363058,Human_Splice_Rec_1363124,Human_Splice_Rec_1363154,Human_Splice_Rec_1363166,Human_Splice_Rec_1363178,Human_Splice_Rec_1363188,Human_Splice_Rec_1363200,Human_Splice_Rec_1363206 RMVar_hsa_circ_156227,RMVar_hsa_circ_96672,RMVar_hsa_circ_69018,RMVar_hsa_circ_301014,RMVar_hsa_circ_361039 85562 RMVar_ID_85562 Human_SNP_ID_500441922 m1A Human chr12 + 48852105 48852105 48852105 CCGGGACTCACCACCCTGAGTCTGAACCGCCCAACGCGGCCTCAACGTCGCGGAGCCGTCGCCAT CCGGGACTCACCACCCTGAGTCTGAACCGCCCGACGCGGCCTCAACGTCGCGGAGCCGTCGCCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:48845532..48852175;chr12:48840026..48852175;chr12:48840069..48852175 26863196 MeRIP-seq:(Medium) rs1313752538 Functional Loss SNV dbSNP153 33..33 33 - - - 85563 RMVar_ID_85563 Human_SNP_ID_500441933 m1A Human chr12 + 48852126 48852126 48852126 CTGAACCGCCCAACGCGGCCTCAACGTCGCGGAGCCGTCGCCATCTTTCCCGTTTCCTGGTCGCG CTGAACCGCCCAACGCGGCCTCAACGTCGCGGCGCCGTCGCCATCTTTCCCGTTTCCTGGTCGCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48851926..48852175 26863196 MeRIP-seq:(Medium) rs1257053230 Functional Loss SNV dbSNP153 33..33 33 - - - 85564 RMVar_ID_85564 Human_SNP_ID_500460485 m1A Human chr12 - 48924650 48924650 48924650 CTAGATGTATGCTCTTGATGCTCTCTCCCCCCAGGGAAGCTTGGTAGATGGACGTATTATTGACA CTAGATGTATGCTCTTGATGCTCTCTCCCCCCGGGGAAGCTTGGTAGATGGACGTATTATTGACA T C AC073610.2,FKBP11 Ensembl:ENSG00000272822,Ensembl:ENSG00000134285 Protein coding,Protein coding intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48924649..48924849 32194978 MeRIP-seq:(Medium) rs112346538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810727,Human_RBP_ID_1269343,Human_RBP_ID_1795817,Human_RBP_ID_5349413,Human_RBP_ID_6189843,Human_RBP_ID_9017598,Human_RBP_ID_22538605,Human_RBP_ID_22645842,Human_RBP_ID_23561370,Human_RBP_ID_24973434 Human_Splice_Rec_1363305,Human_Splice_Rec_1363313,Human_Splice_Rec_1363319,Human_Splice_Rec_1363329,Human_Splice_Rec_1363335,Human_Splice_Rec_1363345,Human_Splice_Rec_1363355,Human_Splice_Rec_1363365,Human_Splice_Rec_1363371,Human_Splice_Rec_1363379,Human_Splice_Rec_1363385 RMVar_hsa_circ_110977,RMVar_hsa_circ_15433,RMVar_hsa_circ_114340,RMVar_hsa_circ_156234,RMVar_hsa_circ_156235 85565 RMVar_ID_85565 Human_SNP_ID_500460486 m1A Human chr12 - 48924650 48924650 48924650 CTAGATGTATGCTCTTGATGCTCTCTCCCCCCAGGGAAGCTTGGTAGATGGACGTATTATTGACA CTAGATGTATGCTCTTGATGCTCTCTCCCCCCCGGGAAGCTTGGTAGATGGACGTATTATTGACA T G AC073610.2,FKBP11 Ensembl:ENSG00000272822,Ensembl:ENSG00000134285 Protein coding,Protein coding intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48924649..48924849 32194978 MeRIP-seq:(Medium) rs112346538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810727,Human_RBP_ID_1269343,Human_RBP_ID_1795817,Human_RBP_ID_5349413,Human_RBP_ID_6189843,Human_RBP_ID_9017598,Human_RBP_ID_22538605,Human_RBP_ID_22645842,Human_RBP_ID_23561370,Human_RBP_ID_24973434 Human_Splice_Rec_1363305,Human_Splice_Rec_1363313,Human_Splice_Rec_1363319,Human_Splice_Rec_1363329,Human_Splice_Rec_1363335,Human_Splice_Rec_1363345,Human_Splice_Rec_1363355,Human_Splice_Rec_1363365,Human_Splice_Rec_1363371,Human_Splice_Rec_1363379,Human_Splice_Rec_1363385 RMVar_hsa_circ_110977,RMVar_hsa_circ_15433,RMVar_hsa_circ_114340,RMVar_hsa_circ_156234,RMVar_hsa_circ_156235 85566 RMVar_ID_85566 Human_SNP_ID_500460820 m1A Human chr12 + 48925372 48925372 48925372 TCGAGCCCAGCCTCAGCCCGGCACACCGCCGCACTGAGCAGCAGCAGCAGCAGCAGATGGAGCGG TCGAGCCCAGCCTCAGCCCGGCACACCGCCGCTCTGAGCAGCAGCAGCAGCAGCAGATGGAGCGG A T CCDC65 Ensembl:ENSG00000139537 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48925036..48925532 32194978 MeRIP-seq:(Medium) rs145495143 Functional Loss SNV dbSNP153 33..33 33 - - - 85567 RMVar_ID_85567 Human_SNP_ID_500461372 m1A Human chr12 + 48927195 48927195 48927195 CCCTATCTCCTGTTTCTGTTAGTGGCTCTGCTACCAGCATTCGTTCTTCTCTCATCTCCCACATC CCCTATCTCCTGTTTCTGTTAGTGGCTCTGCTGCCAGCATTCGTTCTTCTCTCATCTCCCACATC A G CCDC65 Ensembl:ENSG00000139537 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48927146..48927276 26863196 MeRIP-seq:(Medium) rs936822873 Functional Loss SNV dbSNP153 33..33 33 - - - 85568 RMVar_ID_85568 Human_SNP_ID_500464320 m1A Human chr12 + 48937846 48937846 48937846 GAAAATTCTGACCAAGGACAGATGACCCATCCAACCCCTAAGATCAGAAGGGTGGTGGGGCACTG GAAAATTCTGACCAAGGACAGATGACCCATCCGACCCCTAAGATCAGAAGGGTGGTGGGGCACTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48937653..48937852 32194978 MeRIP-seq:(Medium) rs1803047 Functional Loss SNV dbSNP153 33..33 33 - - - 85569 RMVar_ID_85569 Human_SNP_ID_500464680 m1A Human chr12 - 48938960 48938960 48938960 CGAAGGCCTGGACTGGCTGGCCAATCAGCTCAAAAACAAGAAGTGAAAGCCAGACAGCCCTAACA CGAAGGCCTGGACTGGCTGGCCAATCAGCTCAGAAACAAGAAGTGAAAGCCAGACAGCCCTAACA T C ARF3,AC073610.2 Ensembl:ENSG00000134287,Ensembl:ENSG00000272822 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48938594..48939050 32194978 MeRIP-seq:(Medium) rs1208366365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34698,Human_RBP_ID_4224207,Human_RBP_ID_18627359 Human_Splice_Rec_1363247 RMVar_hsa_circ_156239,RMVar_hsa_circ_102971,RMVar_hsa_circ_105792,RMVar_hsa_circ_97456,RMVar_hsa_circ_98247,RMVar_hsa_circ_81388,RMVar_hsa_circ_156240,RMVar_hsa_circ_156237,RMVar_hsa_circ_156238,RMVar_hsa_circ_156241,RMVar_hsa_circ_156236 85570 RMVar_ID_85570 Human_SNP_ID_500465173 m1A Human chr12 - 48941052 48941052 48941052 CTTTGGAAACCTTCTCAAGAGCCTGATTGGGAAGAAGGAGATGCGCATCCTGATGGTGGGCCTGG CTTTGGAAACCTTCTCAAGAGCCTGATTGGGAGGAAGGAGATGCGCATCCTGATGGTGGGCCTGG T C ARF3,AC073610.2 Ensembl:ENSG00000134287,Ensembl:ENSG00000272822 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48941001..48941150 32194978 MeRIP-seq:(Medium) rs1235370712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1166935,Human_RBP_ID_1472395,Human_RBP_ID_1795874,Human_RBP_ID_4255279,Human_RBP_ID_26906790 RMVar_hsa_circ_97456,RMVar_hsa_circ_81388,RMVar_hsa_circ_156237,RMVar_hsa_circ_156241,RMVar_hsa_circ_156236,RMVar_hsa_circ_156243,RMVar_hsa_circ_271325,RMVar_hsa_circ_156244 85571 RMVar_ID_85571 Human_SNP_ID_500468639 m1A Human chr12 + 48956176 48956173 48956176 TGTTGCACTGACCCAAGCAATCAGACTCTTGCAGCAGATCTCCTCCCAATAAAACTTTCATGCCA TGTTGCACTGACCCAAGCAATCAGACTCTT___GCAGATCTCCTCCCAATAAAACTTTCATGCCA TGCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:48956173..48956585 26863196 MeRIP-seq:(Medium) rs775270236 Functional Loss DEL dbSNP153 31..33 33 - - - 85572 RMVar_ID_85572 Human_SNP_ID_500468953 m1A Human chr12 - 48957322 48957322 48957322 GGGCAGAGGCGGCGGCCGCAGCGGCGCAGCTGATAGCAGGAACAGGTGAGAGGCTGGGAAGGGAA GGGCAGAGGCGGCGGCCGCAGCGGCGCAGCTGGTAGCAGGAACAGGTGAGAGGCTGGGAAGGGAA T C ARF3,AC073610.2 Ensembl:ENSG00000134287,Ensembl:ENSG00000272822 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:48957301..48957475 26863196 MeRIP-seq:(Medium) rs1345619418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4224245,Human_RBP_ID_8940706,Human_RBP_ID_9416788,Human_RBP_ID_22436996,Human_RBP_ID_22737023,Human_RBP_ID_26321392 Human_Splice_Rec_1363237,Human_Splice_Rec_1363389,Human_Splice_Rec_1363397,Human_Splice_Rec_1363399,Human_Splice_Rec_1363405,Human_Splice_Rec_1363421,Human_Splice_Rec_1363439 RMVar_hsa_circ_81388,RMVar_hsa_circ_156236 85573 RMVar_ID_85573 Human_SNP_ID_500468954 m1A Human chr12 + 48957324 48957324 48957324 CCCTTCCCAGCCTCTCACCTGTTCCTGCTATCAGCTGCGCCGCTGCGGCCGCCGCCTCTGCCCCG CCCTTCCCAGCCTCTCACCTGTTCCTGCTATCGGCTGCGCCGCTGCGGCCGCCGCCTCTGCCCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:48957301..48957325 26863196 MeRIP-seq:(Medium) rs1416647635 Functional Loss SNV dbSNP153 33..33 33 - - - 85574 RMVar_ID_85574 Human_SNP_ID_500472267 m1A Human chr12 - 48970249 48970249 48970249 TTGACGCTGTCCGGCCTGAGCAAGCGGCAGCTAGGCCTGTGCCTGCGCAACCCCGACGTGACGGC TTGACGCTGTCCGGCCTGAGCAAGCGGCAGCTGGGCCTGTGCCTGCGCAACCCCGACGTGACGGC T C WNT10B Ensembl:ENSG00000169884 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48970198..48970279 32194978 MeRIP-seq:(Medium) rs746771104 Functional Loss SNV dbSNP153 33..33 33 - - - 85575 RMVar_ID_85575 Human_SNP_ID_500472650 m1A Human chr12 + 48971692 48971692 48971692 ATCGAGAGAGCTAGCAAGCCGGCGAGCAAAGGACTGGGGGCTCTGGCTTTGCTCTCACCGAGCTC ATCGAGAGAGCTAGCAAGCCGGCGAGCAAAGGGCTGGGGGCTCTGGCTTTGCTCTCACCGAGCTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:48971646..48971807;chr12:48971582..48971724 26863196 MeRIP-seq:(Medium) rs1214227827 Functional Loss SNV dbSNP153 33..33 33 - - - 85576 RMVar_ID_85576 Human_SNP_ID_500472674 m1A Human chr12 + 48971783 48971783 48971783 CTGCAGCCCCTCCCCGAGCCTGGGGCTTCCCCACCCTACCCTCCACTCCCAGCCTTGACCAGGCG CTGCAGCCCCTCCCCGAGCCTGGGGCTTCCCCTCCCTACCCTCCACTCCCAGCCTTGACCAGGCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:48971656..48971786 26863196 MeRIP-seq:(Medium) rs1051881335 Functional Loss SNV dbSNP153 33..33 33 - - - 85577 RMVar_ID_85577 Human_SNP_ID_500479720 m1A Human chr12 - 48997496 48997496 48997496 GAAGGCGTCTTTGTCATTGACGCCACGTGCGTAGTGATACGATCCCAATATGTTCCAACCCCCCG GAAGGCGTCTTTGTCATTGACGCCACGTGCGTGGTGATACGATCCCAATATGTTCCAACCCCCCG T C DDN Ensembl:ENSG00000181418 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48997447..48997948 26863196 MeRIP-seq:(Medium) rs1173424766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18627387 85578 RMVar_ID_85578 Human_SNP_ID_500485310 m1A Human chr12 + 49018691 49018691 49018691 TCCCGGTCTCCTAAGGGTTGGGGGGGTGTCTTAGGCTCCACAGCGCCCCCGACCGCCCTCCTGCA TCCCGGTCTCCTAAGGGTTGGGGGGGTGTCTTTGGCTCCACAGCGCCCCCGACCGCCCTCCTGCA A T DDN-AS1 Ensembl:ENSG00000257913 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49018689..49018759 26863196 MeRIP-seq:(Medium) rs374002947 Functional Loss SNV dbSNP153 33..33 33 - - - 85579 RMVar_ID_85579 Human_SNP_ID_500486468 m1A Human chr12 - 49022768 49022768 49022768 CAGCAAGCAGTTTGTGCACTCCAAGTCATCTCAGTACCGGCGGCTGCGCACCGAATGGAAGAACA CAGCAAGCAGTTTGTGCACTCCAAGTCATCTCGGTACCGGCGGCTGCGCACCGAATGGAAGAACA T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49022667..49022863 26863196 MeRIP-seq:(Medium) rs750674319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992504,Human_RBP_ID_8781938,Human_RBP_ID_11954047,Human_RBP_ID_17238667,Human_RBP_ID_18434241,Human_RBP_ID_22174128 Human_miRNA_ID_300556,Human_miRNA_ID_1381421,Human_miRNA_ID_2065439,Human_miRNA_ID_2703304,Human_miRNA_ID_2934613,Human_miRNA_ID_3010676 RMVar_hsa_circ_29484,RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253 85580 RMVar_ID_85580 Human_SNP_ID_500487590 m1A Human chr12 - 49027122 49027122 49027122 ACCGAACCCTTGGCTGAGCCACCCGTCCCCTCACCTCTGCCACTGGCCTCATCCCCTGAATCAGC ACCGAACCCTTGGCTGAGCCACCCGTCCCCTCGCCTCTGCCACTGGCCTCATCCCCTGAATCAGC T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:49027076..49027231 26863196 MeRIP-seq:(Medium) rs763631585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877755,Human_RBP_ID_8787198,Human_RBP_ID_9278945,Human_RBP_ID_18188743,Human_RBP_ID_18935206,Human_RBP_ID_22040311,Human_RBP_ID_27214730,Human_RBP_ID_27422183 Human_miRNA_ID_873619,Human_miRNA_ID_1231709,Human_miRNA_ID_1559254,Human_miRNA_ID_2273006 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_88626,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_14104,RMVar_hsa_circ_156255 85581 RMVar_ID_85581 Human_SNP_ID_500487591 m1A Human chr12 - 49027122 49027122 49027122 ACCGAACCCTTGGCTGAGCCACCCGTCCCCTCACCTCTGCCACTGGCCTCATCCCCTGAATCAGC ACCGAACCCTTGGCTGAGCCACCCGTCCCCTCCCCTCTGCCACTGGCCTCATCCCCTGAATCAGC T G KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:49027076..49027231 26863196 MeRIP-seq:(Medium) rs763631585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877755,Human_RBP_ID_8787198,Human_RBP_ID_9278945,Human_RBP_ID_18188743,Human_RBP_ID_18935206,Human_RBP_ID_22040311,Human_RBP_ID_27214730,Human_RBP_ID_27422183 Human_miRNA_ID_873619,Human_miRNA_ID_1231709,Human_miRNA_ID_1559254,Human_miRNA_ID_2273006 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_88626,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_14104,RMVar_hsa_circ_156255 85582 RMVar_ID_85582 Human_SNP_ID_500487611 m1A Human chr12 - 49027154 49027154 49027154 GTCCCCCTACTGAGCCCTTGGTTGAACTTCCCACCGAACCCTTGGCTGAGCCACCCGTCCCCTCA GTCCCCCTACTGAGCCCTTGGTTGAACTTCCCGCCGAACCCTTGGCTGAGCCACCCGTCCCCTCA T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49027103..49027253 26863196 MeRIP-seq:(Medium) rs778051166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992509,Human_RBP_ID_4224529,Human_RBP_ID_11954098,Human_RBP_ID_18188743,Human_RBP_ID_18935206,Human_RBP_ID_22040311,Human_RBP_ID_23561695,Human_RBP_ID_27422183,Human_RBP_ID_27557993 Human_miRNA_ID_676261,Human_miRNA_ID_2269693 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_88626,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_14104,RMVar_hsa_circ_156255 85583 RMVar_ID_85583 Human_SNP_ID_500487612 m1A Human chr12 - 49027154 49027154 49027154 GTCCCCCTACTGAGCCCTTGGTTGAACTTCCCACCGAACCCTTGGCTGAGCCACCCGTCCCCTCA GTCCCCCTACTGAGCCCTTGGTTGAACTTCCCCCCGAACCCTTGGCTGAGCCACCCGTCCCCTCA T G KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49027103..49027253 26863196 MeRIP-seq:(Medium) rs778051166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992509,Human_RBP_ID_4224529,Human_RBP_ID_11954098,Human_RBP_ID_18188743,Human_RBP_ID_18935206,Human_RBP_ID_22040311,Human_RBP_ID_23561695,Human_RBP_ID_27422183,Human_RBP_ID_27557993 Human_miRNA_ID_676261,Human_miRNA_ID_2269693 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_88626,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_14104,RMVar_hsa_circ_156255 85584 RMVar_ID_85584 Human_SNP_ID_500489129 m1A Human chr12 - 49031657 49031657 49031657 CCCATCCAGGGACCCCCAAACCTCAGGGGCCAACCTTGGAGCCGCCTCCTGGGAGGGTCTCACCT CCCATCCAGGGACCCCCAAACCTCAGGGGCCAGCCTTGGAGCCGCCTCCTGGGAGGGTCTCACCT T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:49031626..49031700 26863196 MeRIP-seq:(Medium) rs1222329781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357556,Human_RBP_ID_18469308,Human_RBP_ID_22040570,Human_RBP_ID_27422199 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_82068,RMVar_hsa_circ_156260,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268 85585 RMVar_ID_85585 Human_SNP_ID_500492473 m1A Human chr12 + 49040653 49040653 49040653 CAATGGGGGCTGAGCATATGGGTCAGTGTAGGAGCCAGGGCGAAAGATGTCTGGGTGACTTGGAG CAATGGGGGCTGAGCATATGGGTCAGTGTAGGCGCCAGGGCGAAAGATGTCTGGGTGACTTGGAG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:49040493..49040716 26863410 MeRIP-seq:(Medium) rs1442137943 Functional Loss SNV dbSNP153 33..33 33 - - - 85586 RMVar_ID_85586 Human_SNP_ID_500492507 m1A Human chr12 - 49040746 49040719 49040746 TGACCCCTCGGGCATCTCAGGTAGAGCCCCAGAGCCCGGGCTTGGGCCTAAGGCCCCAGGAGCCA TGACCCCTCGGGCATCTCAGGTAGAGCCCCAG___________________________GAGCCA CCTGGGGCCTTAGGCCCAAGCCCGGGCT C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:49040726..49040750 26863196 MeRIP-seq:(Medium) rs1481442670 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_754089,Human_RBP_ID_11954180,Human_RBP_ID_17074815,Human_RBP_ID_22794175 Human_miRNA_ID_2424620,Human_miRNA_ID_2434282,Human_miRNA_ID_2577361,Human_miRNA_ID_3069310 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156269,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268,RMVar_hsa_circ_107500,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482 85587 RMVar_ID_85587 Human_SNP_ID_500492605 m1A Human chr12 - 49040915 49040915 49040915 CCCCCACCTTTTGGGGAGTCCCGGAAGGCCCTAGAGGTGAAGAAGGAAGAGCTTGGGGCATCCTC CCCCCACCTTTTGGGGAGTCCCGGAAGGCCCTGGAGGTGAAGAAGGAAGAGCTTGGGGCATCCTC T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49040864..49040969 32194978 MeRIP-seq:(Medium) rs1266537084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810448,Human_RBP_ID_1065455,Human_RBP_ID_5127107,Human_RBP_ID_22040580,Human_RBP_ID_24973870 Human_miRNA_ID_2008787 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156269,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268,RMVar_hsa_circ_107500,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482 85588 RMVar_ID_85588 Human_SNP_ID_500492690 m1A Human chr12 - 49041101 49041101 49041101 GGCGCCTCATCTCGTCCTGGGGCTGGCCAGCCAGGGGAATTCCACACTACCCCACCTGGCACCCC GGCGCCTCATCTCGTCCTGGGGCTGGCCAGCCGGGGGAATTCCACACTACCCCACCTGGCACCCC T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49041051..49041375 26863196 MeRIP-seq:(Medium) rs768256072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126851,Human_RBP_ID_6190392,Human_RBP_ID_8782152,Human_RBP_ID_11954196,Human_RBP_ID_17075275,Human_RBP_ID_17357567 Human_miRNA_ID_793237,Human_miRNA_ID_2061539,Human_miRNA_ID_2332141,Human_miRNA_ID_2436726,Human_miRNA_ID_2965226 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156269,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268,RMVar_hsa_circ_107500,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482 85589 RMVar_ID_85589 Human_SNP_ID_500492785 m1A Human chr12 - 49041249 49041249 49041249 CCCACCCCAGGTGCCCGCCCAAGTGCCTTCGCAGGACCCCTTTGGACTGGCCCCTGCCTATCCCC CCCACCCCAGGTGCCCGCCCAAGTGCCTTCGCGGGACCCCTTTGGACTGGCCCCTGCCTATCCCC T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:49041149..49041329 26863196 MeRIP-seq:(Medium) rs557789686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5127109,Human_RBP_ID_6190393,Human_RBP_ID_8782155,Human_RBP_ID_11954197,Human_RBP_ID_18160184,Human_RBP_ID_18627502,Human_RBP_ID_22572481,Human_RBP_ID_24973886,Human_RBP_ID_27558001 Human_miRNA_ID_1335968,Human_miRNA_ID_1352953,Human_miRNA_ID_2657149,Human_miRNA_ID_2662499 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156269,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268,RMVar_hsa_circ_107500,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482 85590 RMVar_ID_85590 Human_SNP_ID_500493902 m1A Human chr12 - 49044253 49044251 49044253 GCGACAGCGGAAATCCCACACACGCACGAAAAAGGGGCCTGCTGCACAGGCGGAGGTGTTGAGTG GCGACAGCGGAAATCCCACACACGCACGAAAA__GGGCCTGCTGCACAGGCGGAGGTGTTGAGTG CCT C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49043891..49044490 26863196 MeRIP-seq:(Medium) rs1555194236 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6190414,Human_RBP_ID_8782204 Human_Splice_Rec_1363826,Human_Splice_Rec_1363827,Human_Splice_Rec_1363914,Human_Splice_Rec_1363915 Clinvar_Rec_448 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_83103,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_74752,RMVar_hsa_circ_102062,RMVar_hsa_circ_107987,RMVar_hsa_circ_156275,RMVar_hsa_circ_156276,RMVar_hsa_circ_104332,RMVar_hsa_circ_156277,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279 85591 RMVar_ID_85591 Human_SNP_ID_500493903 m1A Human chr12 - 49044253 49044253 49044253 GCGACAGCGGAAATCCCACACACGCACGAAAAAGGGGCCTGCTGCACAGGCGGAGGTGTTGAGTG GCGACAGCGGAAATCCCACACACGCACGAAAAGGGGGCCTGCTGCACAGGCGGAGGTGTTGAGTG T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49043891..49044490 26863196 MeRIP-seq:(Medium) rs780141969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6190414,Human_RBP_ID_8782204 Human_Splice_Rec_1363826,Human_Splice_Rec_1363827,Human_Splice_Rec_1363914,Human_Splice_Rec_1363915 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_83103,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_74752,RMVar_hsa_circ_102062,RMVar_hsa_circ_107987,RMVar_hsa_circ_156275,RMVar_hsa_circ_156276,RMVar_hsa_circ_104332,RMVar_hsa_circ_156277,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279 85592 RMVar_ID_85592 Human_SNP_ID_500493970 m1A Human chr12 - 49044413 49044413 49044413 ACCGAGGAAAGCAAAAAACGCAAGCGTAAACCATATCGGCCTGGTGAGGTCCTGGGATGGGGTTG ACCGAGGAAAGCAAAAAACGCAAGCGTAAACCTTATCGGCCTGGTGAGGTCCTGGGATGGGGTTG T A KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49044406..49044481 26863196 MeRIP-seq:(Medium) rs768138617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942867,Human_RBP_ID_5555309 Human_Splice_Rec_1363825,Human_Splice_Rec_1363913 Human_miRNA_ID_2298543,Human_miRNA_ID_2923776 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_83103,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_74752,RMVar_hsa_circ_102062,RMVar_hsa_circ_107987,RMVar_hsa_circ_156275,RMVar_hsa_circ_156276,RMVar_hsa_circ_104332,RMVar_hsa_circ_156277,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279 85593 RMVar_ID_85593 Human_SNP_ID_500493971 m1A Human chr12 - 49044413 49044413 49044413 ACCGAGGAAAGCAAAAAACGCAAGCGTAAACCATATCGGCCTGGTGAGGTCCTGGGATGGGGTTG ACCGAGGAAAGCAAAAAACGCAAGCGTAAACCGTATCGGCCTGGTGAGGTCCTGGGATGGGGTTG T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49044406..49044481 26863196 MeRIP-seq:(Medium) rs768138617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942867,Human_RBP_ID_5555309 Human_Splice_Rec_1363825,Human_Splice_Rec_1363913 Human_miRNA_ID_2298543,Human_miRNA_ID_2923776 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_83103,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_74752,RMVar_hsa_circ_102062,RMVar_hsa_circ_107987,RMVar_hsa_circ_156275,RMVar_hsa_circ_156276,RMVar_hsa_circ_104332,RMVar_hsa_circ_156277,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279 85594 RMVar_ID_85594 Human_SNP_ID_500496441 m1A Human chr12 - 49051484 49051484 49051484 TCACCCCTGTTGCCACTACCTGAGGAGCCGCAACTCTGCCCCCGGTCCGAGGGGCCGCACCTGTC TCACCCCTGTTGCCACTACCTGAGGAGCCGCACCTCTGCCCCCGGTCCGAGGGGCCGCACCTGTC T G KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49051433..49051765 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_754108,Human_RBP_ID_877813,Human_RBP_ID_5521519,Human_RBP_ID_9364895,Human_RBP_ID_11954265,Human_RBP_ID_17356962,Human_RBP_ID_17650634,Human_RBP_ID_17820411,Human_RBP_ID_19825920,Human_RBP_ID_22039278,Human_RBP_ID_22794204,Human_RBP_ID_23208044,Human_RBP_ID_26321411 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_102062,RMVar_hsa_circ_156275,RMVar_hsa_circ_104332,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279,RMVar_hsa_circ_156280,RMVar_hsa_circ_85177 85595 RMVar_ID_85595 Human_SNP_ID_500496504 m1A Human chr12 - 49051607 49051607 49051607 CCTCCACCTGAGGCTTCACGCCTCTCCCCACCACCTGAGGACTCCCCCACATCCCCACCACCTGA CCTCCACCTGAGGCTTCACGCCTCTCCCCACCGCCTGAGGACTCCCCCACATCCCCACCACCTGA T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49051558..49052000 26863196 MeRIP-seq:(Medium) rs1183564910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1235992,Human_RBP_ID_5126861,Human_RBP_ID_17074821,Human_RBP_ID_17357574,Human_RBP_ID_18935221,Human_RBP_ID_22174290,Human_RBP_ID_27422329 Human_miRNA_ID_1701651,Human_miRNA_ID_2297509 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_102062,RMVar_hsa_circ_156275,RMVar_hsa_circ_104332,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279,RMVar_hsa_circ_156280,RMVar_hsa_circ_85177 85596 RMVar_ID_85596 Human_SNP_ID_500496556 m1A Human chr12 + 49051694 49051694 49051694 GGTGGGGACAAGGGAGATTCCTCAGGCGGTGGAGACAGGCGTGACACCACAGGCAGGGGGGATAG GGTGGGGACAAGGGAGATTCCTCAGGCGGTGGGGACAGGCGTGACACCACAGGCAGGGGGGATAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:49051393..49051825;chr12:49051676..49051700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 85597 RMVar_ID_85597 Human_SNP_ID_500496717 m1A Human chr12 + 49051973 49051973 49051973 ATGGGTGACTCCTCAGGTGGTGGAGACAGGCGAGATGCTTCAGGTGGCGGGGAAGTGGGCAATTC ATGGGTGACTCCTCAGGTGGTGGAGACAGGCGTGATGCTTCAGGTGGCGGGGAAGTGGGCAATTC A T NONHSAG011077.2 RNACentral:URS00008C15BB lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:49051431..49052294 26863196 MeRIP-seq:(Medium) rs1350370171 Functional Loss SNV dbSNP153 33..33 33 - - - 85598 RMVar_ID_85598 Human_SNP_ID_500496734 m1A Human chr12 + 49052001 49052001 49052001 GGCGAGATGCTTCAGGTGGCGGGGAAGTGGGCAATTCCTCAGGTGGCGGGGACAAAGGAGATTCT GGCGAGATGCTTCAGGTGGCGGGGAAGTGGGCGATTCCTCAGGTGGCGGGGACAAAGGAGATTCT A G NONHSAG011077.2 RNACentral:URS00008C15BB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49051882..49052572 26863196 MeRIP-seq:(Medium) rs1351651538 Functional Loss SNV dbSNP153 33..33 33 - - - 85599 RMVar_ID_85599 Human_SNP_ID_500499136 m1A Human chr12 - 49060387 49060387 49060387 AGCCGGCCAGGCCGGGGGCGGGGCAGCTCCCGAGGCCAGAGGGGAAGGGAGGCGAGCGCAGGGCC AGCCGGCCAGGCCGGGGGCGGGGCAGCTCCCGGGGCCAGAGGGGAAGGGAGGCGAGCGCAGGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49060066..49060731 26863196 MeRIP-seq:(Medium) rs969346850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26907066 85600 RMVar_ID_85600 Human_SNP_ID_500517149 m1A Human chr12 - 49128045 49128045 49128045 ATGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAAGATATGGCTGCCCTTGAGAAGGATTATGAGGA ATGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAGGATATGGCTGCCCTTGAGAAGGATTATGAGGA T C TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:49127889..49128129;chr12:49127854..49128107;chr12:49127949..49128108 26863196 MeRIP-seq:(Medium) rs747107430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228881,Human_RBP_ID_420803,Human_RBP_ID_878224,Human_RBP_ID_1472603,Human_RBP_ID_4255538,Human_RBP_ID_5111439,Human_RBP_ID_5256667,Human_RBP_ID_9017657,Human_RBP_ID_9278975,Human_RBP_ID_11954538,Human_RBP_ID_17820452,Human_RBP_ID_22039304,Human_RBP_ID_22435825,Human_RBP_ID_22493316,Human_RBP_ID_22756724,Human_RBP_ID_23561775,Human_RBP_ID_26768246,Human_RBP_ID_27214908 Human_miRNA_ID_2781390,Human_miRNA_ID_2786956 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 85601 RMVar_ID_85601 Human_SNP_ID_500517262 m1A Human chr12 - 49128795 49128795 49128795 AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCAGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCTGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC T A TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK-293T cells,m1A-quant-seq;HTR8/Svneo,Normoxia chr12:49128724..49129015 31548705,32194978 m1A-quant-seq:(High) rs1057725 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_420813,Human_RBP_ID_753565,Human_RBP_ID_878225,Human_RBP_ID_992560,Human_RBP_ID_1235996,Human_RBP_ID_1269398,Human_RBP_ID_1357654,Human_RBP_ID_1472606,Human_RBP_ID_1796026,Human_RBP_ID_3406908,Human_RBP_ID_4255543,Human_RBP_ID_5140265,Human_RBP_ID_6190547,Human_RBP_ID_8377113,Human_RBP_ID_11954544,Human_RBP_ID_17238736,Human_RBP_ID_17354536,Human_RBP_ID_17471580,Human_RBP_ID_17820454,Human_RBP_ID_18188768,Human_RBP_ID_18627625,Human_RBP_ID_22435827,Human_RBP_ID_22532421,Human_RBP_ID_22794225,Human_RBP_ID_23561779,Human_RBP_ID_26907086,Human_RBP_ID_27214911,Human_RBP_ID_27629902 Human_miRNA_ID_2723904 Clinvar_Rec_449,Clinvar_Rec_450 GWAS_ID_10157,GWAS_ID_10158,GWAS_ID_10159,GWAS_ID_10160,GWAS_ID_10161,GWAS_ID_10162,GWAS_ID_10163,GWAS_ID_10164,GWAS_ID_10165,GWAS_ID_10166,GWAS_ID_10167,GWAS_ID_10168,GWAS_ID_10169,GWAS_ID_10170,GWAS_ID_10171,GWAS_ID_10172,GWAS_ID_10173,GWAS_ID_10174,GWAS_ID_10175,GWAS_ID_10176,GWAS_ID_10177,GWAS_ID_10178,GWAS_ID_10179,GWAS_ID_10180,GWAS_ID_10181,GWAS_ID_10182,GWAS_ID_10183,GWAS_ID_10184,GWAS_ID_10185,GWAS_ID_10186,GWAS_ID_10187,GWAS_ID_10188,GWAS_ID_10189,GWAS_ID_10190,GWAS_ID_10191,GWAS_ID_10192,GWAS_ID_10193,GWAS_ID_10194,GWAS_ID_10195,GWAS_ID_10196,GWAS_ID_10197,GWAS_ID_10198,GWAS_ID_10199,GWAS_ID_10200 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 85602 RMVar_ID_85602 Human_SNP_ID_500517263 m1A Human chr12 - 49128795 49128795 49128795 AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCAGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCGGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC T C TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK-293T cells,m1A-quant-seq;HTR8/Svneo,Normoxia chr12:49128724..49129015 31548705,32194978 m1A-quant-seq:(High) rs1057725 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_420813,Human_RBP_ID_753565,Human_RBP_ID_878225,Human_RBP_ID_992560,Human_RBP_ID_1235996,Human_RBP_ID_1269398,Human_RBP_ID_1357654,Human_RBP_ID_1472606,Human_RBP_ID_1796026,Human_RBP_ID_3406908,Human_RBP_ID_4255543,Human_RBP_ID_5140265,Human_RBP_ID_6190547,Human_RBP_ID_8377113,Human_RBP_ID_11954544,Human_RBP_ID_17238736,Human_RBP_ID_17354536,Human_RBP_ID_17471580,Human_RBP_ID_17820454,Human_RBP_ID_18188768,Human_RBP_ID_18627625,Human_RBP_ID_22435827,Human_RBP_ID_22532421,Human_RBP_ID_22794225,Human_RBP_ID_23561779,Human_RBP_ID_26907086,Human_RBP_ID_27214911,Human_RBP_ID_27629902 Human_miRNA_ID_2723904 Clinvar_Rec_449,Clinvar_Rec_450 GWAS_ID_10157,GWAS_ID_10158,GWAS_ID_10159,GWAS_ID_10160,GWAS_ID_10161,GWAS_ID_10162,GWAS_ID_10163,GWAS_ID_10164,GWAS_ID_10165,GWAS_ID_10166,GWAS_ID_10167,GWAS_ID_10168,GWAS_ID_10169,GWAS_ID_10170,GWAS_ID_10171,GWAS_ID_10172,GWAS_ID_10173,GWAS_ID_10174,GWAS_ID_10175,GWAS_ID_10176,GWAS_ID_10177,GWAS_ID_10178,GWAS_ID_10179,GWAS_ID_10180,GWAS_ID_10181,GWAS_ID_10182,GWAS_ID_10183,GWAS_ID_10184,GWAS_ID_10185,GWAS_ID_10186,GWAS_ID_10187,GWAS_ID_10188,GWAS_ID_10189,GWAS_ID_10190,GWAS_ID_10191,GWAS_ID_10192,GWAS_ID_10193,GWAS_ID_10194,GWAS_ID_10195,GWAS_ID_10196,GWAS_ID_10197,GWAS_ID_10198,GWAS_ID_10199,GWAS_ID_10200 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 85603 RMVar_ID_85603 Human_SNP_ID_500518063 m1A Human chr12 - 49131106 49131106 49131106 CCTCGGTGTGTGTAAATAGCGGGGGCCCGGAAAGGTCGAGGGGCGCCAGGATTTCTTCTCGGACT CCTCGGTGTGTGTAAATAGCGGGGGCCCGGAAGGGTCGAGGGGCGCCAGGATTTCTTCTCGGACT T C TUBA1B Ensembl:ENSG00000123416 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49131100..49131292 26863196 MeRIP-seq:(Medium) rs770955588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3664,Human_RBP_ID_810460,Human_RBP_ID_18478997,Human_RBP_ID_22353806 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_46900,RMVar_hsa_circ_156305 85604 RMVar_ID_85604 Human_SNP_ID_500518076 m1A Human chr12 - 49131163 49131163 49131163 AGCCGTCCGTTTGGAGGGCGGAAAACGAGGCGAGAGGCCAGGGCGGGAGTGGTGAGACCTCGGTG AGCCGTCCGTTTGGAGGGCGGAAAACGAGGCGGGAGGCCAGGGCGGGAGTGGTGAGACCTCGGTG T C TUBA1B Ensembl:ENSG00000123416 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49131161..49131274 32194978 MeRIP-seq:(Medium) rs997537552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5348301,Human_RBP_ID_6190564,Human_RBP_ID_22353806 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_46900,RMVar_hsa_circ_156305 85605 RMVar_ID_85605 Human_SNP_ID_500518187 m1A Human chr12 - 49131354 49131354 49131354 CTTACCTCGACTCTTAGCTTGTCGGGGACGGTAACCGGGACCCGGTGTCTGCTCCTGTCGCCTTC CTTACCTCGACTCTTAGCTTGTCGGGGACGGTGACCGGGACCCGGTGTCTGCTCCTGTCGCCTTC T C TUBA1B Ensembl:ENSG00000123416 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49131351..49131400 26863196 MeRIP-seq:(Medium) rs199627080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228887,Human_RBP_ID_269467,Human_RBP_ID_420827,Human_RBP_ID_753568,Human_RBP_ID_992568,Human_RBP_ID_1166978,Human_RBP_ID_1269403,Human_RBP_ID_1472625,Human_RBP_ID_1796034,Human_RBP_ID_3406912,Human_RBP_ID_4246078,Human_RBP_ID_5257138,Human_RBP_ID_5273967,Human_RBP_ID_5314542,Human_RBP_ID_5417052,Human_RBP_ID_5437715,Human_RBP_ID_5461846,Human_RBP_ID_5491570,Human_RBP_ID_6190567,Human_RBP_ID_8377126,Human_RBP_ID_8782340,Human_RBP_ID_9322492,Human_RBP_ID_17356977,Human_RBP_ID_17471586,Human_RBP_ID_17820463,Human_RBP_ID_18188771,Human_RBP_ID_18417649,Human_RBP_ID_18627637,Human_RBP_ID_22174369,Human_RBP_ID_22435832,Human_RBP_ID_22493319,Human_RBP_ID_22532422,Human_RBP_ID_22794228,Human_RBP_ID_23207613,Human_RBP_ID_23561794,Human_RBP_ID_26907095,Human_RBP_ID_27154824,Human_RBP_ID_27214922,Human_RBP_ID_27629906 Human_Splice_Rec_1364339,Human_Splice_Rec_1364349,Human_Splice_Rec_1364357,Human_Splice_Rec_1364365,Human_Splice_Rec_1364371,Human_Splice_Rec_1364377 Human_miRNA_ID_2582263,Human_miRNA_ID_2582264 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_121306,RMVar_hsa_circ_46900,RMVar_hsa_circ_156305,RMVar_hsa_circ_156306 85606 RMVar_ID_85606 Human_SNP_ID_500518217 m1A Human chr12 + 49131389 49131389 49131389 CGTCCCCGACAAGCTAAGAGTCGAGGTAAGTAACGCACTAGGGCGGGGCCGGCGCTGGAGCCTCT CGTCCCCGACAAGCTAAGAGTCGAGGTAAGTAGCGCACTAGGGCGGGGCCGGCGCTGGAGCCTCT A G AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:49131376..49131400 26863196 MeRIP-seq:(Medium) rs1037825196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1364386 85607 RMVar_ID_85607 Human_SNP_ID_500522401 m1A Human chr12 - 49145505 49145505 49145505 CAACACGACCTCCCCTCTGCACTTTTTAACCAACTATTACTGCCTAATCAACATCTCTACTTATA CAACACGACCTCCCCTCTGCACTTTTTAACCACCTATTACTGCCTAATCAACATCTCTACTTATA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49145502..49145595 26863196 MeRIP-seq:(Medium) rs1170895468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121306,RMVar_hsa_circ_156305,RMVar_hsa_circ_156306 85608 RMVar_ID_85608 Human_SNP_ID_500532448 m1A Human chr12 - 49185359 49185359 49185359 CAAAGATGTCAATGCTGCCATTGCCACCATCAAGACCAAGCGTACCATCCAGTTTGTGGATTGGT CAAAGATGTCAATGCTGCCATTGCCACCATCAGGACCAAGCGTACCATCCAGTTTGTGGATTGGT T C TUBA1A Ensembl:ENSG00000167552 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49185291..49185400 32194978 MeRIP-seq:(Medium) rs1565627040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4225232,Human_RBP_ID_26805617 Human_miRNA_ID_1957194,Human_miRNA_ID_1957195 Clinvar_Rec_451 RMVar_hsa_circ_85539,RMVar_hsa_circ_113862,RMVar_hsa_circ_121306,RMVar_hsa_circ_156305,RMVar_hsa_circ_268750,RMVar_hsa_circ_156306,RMVar_hsa_circ_121025,RMVar_hsa_circ_91159,RMVar_hsa_circ_156308,RMVar_hsa_circ_156309,RMVar_hsa_circ_156310,RMVar_hsa_circ_156307 85609 RMVar_ID_85609 Human_SNP_ID_500551548 m1A Human chr12 - 49264795 49264786 49264795 AGGGGAGGAAGGGGAGGAAGGGGAGGAAGGGCAGGAAGGGCTCTGGGGCTGGAGAATGGGCCGGG AGGGGAGGAAGGGGAGGAAGGGGAGGAAGGGC_________TCTGGGGCTGGAGAATGGGCCGGG AGCCCTTCCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49264609..49264832 26863196 MeRIP-seq:(Medium) rs1253171550 Functional Loss DEL dbSNP153 33..41 33 - - - 85610 RMVar_ID_85610 Human_SNP_ID_500551745 m1A Human chr12 - 49265103 49265103 49265103 GGCAACAAGGATCTCCCACTAACAGACTACCAAGGAGTCCGGGGGAGAAGTAGTGAAAGGGTGGC GGCAACAAGGATCTCCCACTAACAGACTACCAGGGAGTCCGGGGGAGAAGTAGTGAAAGGGTGGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:49265070..49265169 26863410 MeRIP-seq:(Medium) rs1384882447 Functional Loss SNV dbSNP153 33..33 33 - - - 85611 RMVar_ID_85611 Human_SNP_ID_500551754 m1A Human chr12 - 49265114 49265114 49265114 GGCGAAGGGACGGCAACAAGGATCTCCCACTAACAGACTACCAAGGAGTCCGGGGGAGAAGTAGT GGCGAAGGGACGGCAACAAGGATCTCCCACTAGCAGACTACCAAGGAGTCCGGGGGAGAAGTAGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:49265045..49265242 26863410 MeRIP-seq:(Medium) rs549625036 Functional Loss SNV dbSNP153 33..33 33 - - - 85612 RMVar_ID_85612 Human_SNP_ID_500553119 m1A Human chr12 - 49269416 49269416 49269416 GGAAAATGTCAGGGTATAATACATCAGATGGGACATTTAGGAATGATTCACACCTAATGACTGAT GGAAAATGTCAGGGTATAATACATCAGATGGGGCATTTAGGAATGATTCACACCTAATGACTGAT T C AC125611.3 Ensembl:ENSG00000258232 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49269414..49269525 26863196 MeRIP-seq:(Medium) rs1565649997 Functional Loss SNV dbSNP153 33..33 33 - - - 85613 RMVar_ID_85613 Human_SNP_ID_500554035 m1A Human chr12 + 49272509 49272509 49272509 TGCCTTCATGGTAGACAATGAGGCCATCTATGACATCTGTCGTAGAAACCTCGATATCGAGCGCC TGCCTTCATGGTAGACAATGAGGCCATCTATGCCATCTGTCGTAGAAACCTCGATATCGAGCGCC A C TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1456989996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2534634,Human_miRNA_ID_2536366 RMVar_hsa_circ_118502,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156317,RMVar_hsa_circ_107279,RMVar_hsa_circ_83896,RMVar_hsa_circ_156318,RMVar_hsa_circ_156319 85614 RMVar_ID_85614 Human_SNP_ID_500554216 m1A Human chr12 + 49273169 49273169 49273169 GGCCCGTGAGGACATGGCTGCCCTTGAGAAGGATTATGAGGAGGTTGGAGCAGATAGTGCTGACG GGCCCGTGAGGACATGGCTGCCCTTGAGAAGGTTTATGAGGAGGTTGGAGCAGATAGTGCTGACG A T TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:49273087..49273250 26863196 MeRIP-seq:(Medium) rs1172120959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420873,Human_RBP_ID_1472655,Human_RBP_ID_1796060,Human_RBP_ID_2339968,Human_RBP_ID_3406956,Human_RBP_ID_4225287,Human_RBP_ID_5111441,Human_RBP_ID_6190730,Human_RBP_ID_8377178,Human_RBP_ID_11954999,Human_RBP_ID_17186180,Human_RBP_ID_17650359,Human_RBP_ID_17830273,Human_RBP_ID_19703237,Human_RBP_ID_22437013,Human_RBP_ID_23561898,Human_RBP_ID_26423658 Human_miRNA_ID_1473728 RMVar_hsa_circ_118502,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156317,RMVar_hsa_circ_107279,RMVar_hsa_circ_83896,RMVar_hsa_circ_156318,RMVar_hsa_circ_156319 85615 RMVar_ID_85615 Human_SNP_ID_500559660 m1A Human chr12 - 49293607 49293607 49293607 GGCTGGCCAGCTCCTCAGTATTGCAGGGCAGCAGCCCCCTCCCCCCTTTGTGCGTCCTGTGAGAT GGCTGGCCAGCTCCTCAGTATTGCAGGGCAGCCGCCCCCTCCCCCCTTTGTGCGTCCTGTGAGAT T G AC125611.4 Ensembl:ENSG00000258334 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49293572..49293722 26863196 MeRIP-seq:(Medium) rs980031371 Functional Loss SNV dbSNP153 33..33 33 - - - 85616 RMVar_ID_85616 Human_SNP_ID_500560125 m1A Human chr12 - 49295300 49295300 49295300 GCGGCTGCTGGAGAAGCGGGAGCTGGACGAGTAGGAGAAGGCCCCGGGGGATAGTGAGGGCGGTG GCGGCTGCTGGAGAAGCGGGAGCTGGACGAGTGGGAGAAGGCCCCGGGGGATAGTGAGGGCGGTG T C AC125611.4 Ensembl:ENSG00000258334 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49294520..49295393 26863196 MeRIP-seq:(Medium) rs765532063 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5558109 Human_Splice_Rec_1364501 85617 RMVar_ID_85617 Human_SNP_ID_500567851 m1A Human chr12 + 49323666 49323666 49323666 ATCCCCTCCTCCGGGGTGTATCTCCTACCCCTAGCAAGATTCCGGTACGCTCTCAGAAACGCACG ATCCCCTCCTCCGGGGTGTATCTCCTACCCCTGGCAAGATTCCGGTACGCTCTCAGAAACGCACG A G TROAP Ensembl:ENSG00000135451 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:49323578..49323721 26863196 MeRIP-seq:(Medium) rs372584414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420900,Human_RBP_ID_1472662,Human_RBP_ID_4246632,Human_RBP_ID_5555329,Human_RBP_ID_9017693,Human_RBP_ID_17820503,Human_RBP_ID_18627677,Human_RBP_ID_22794238,Human_RBP_ID_26806656 Human_Splice_Rec_1364564,Human_Splice_Rec_1364565,Human_Splice_Rec_1364568,Human_Splice_Rec_1364569,Human_Splice_Rec_1364594,Human_Splice_Rec_1364595,Human_Splice_Rec_1364600,Human_Splice_Rec_1364601,Human_Splice_Rec_1364606,Human_Splice_Rec_1364607,Human_Splice_Rec_1364620,Human_Splice_Rec_1364621,Human_Splice_Rec_1364648,Human_Splice_Rec_1364649,Human_Splice_Rec_1364658,Human_Splice_Rec_1364659,Human_Splice_Rec_1364662,Human_Splice_Rec_1364663,Human_Splice_Rec_1364680,Human_Splice_Rec_1364682,Human_Splice_Rec_1364683,Human_Splice_Rec_1364698,Human_Splice_Rec_1364699,Human_Splice_Rec_1364718,Human_Splice_Rec_1364719,Human_Splice_Rec_1364731 RMVar_hsa_circ_53245 85618 RMVar_ID_85618 Human_SNP_ID_500567886 m1A Human chr12 + 49323745 49323745 49323745 TACATCGTGCGCCGTGGACCAGGAGAACCAAGATCCAAGGGTAAGAGGGGCCTAATGGGGGAAGA TACATCGTGCGCCGTGGACCAGGAGAACCAAGTTCCAAGGGTAAGAGGGGCCTAATGGGGGAAGA A T TROAP Ensembl:ENSG00000135451 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:49323726..49323750 26863196 MeRIP-seq:(Medium) rs755810246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111698,Human_RBP_ID_18977094 Human_Splice_Rec_1364565,Human_Splice_Rec_1364569,Human_Splice_Rec_1364595,Human_Splice_Rec_1364601,Human_Splice_Rec_1364607,Human_Splice_Rec_1364621,Human_Splice_Rec_1364649,Human_Splice_Rec_1364659,Human_Splice_Rec_1364663,Human_Splice_Rec_1364683,Human_Splice_Rec_1364699,Human_Splice_Rec_1364719,Human_Splice_Rec_1364731 RMVar_hsa_circ_53245 85619 RMVar_ID_85619 Human_SNP_ID_500568092 m1A Human chr12 - 49324260 49324260 49324260 TCCAGTGATCCTCCTGCTTCAGCCTCCTGAGTAGCTGTGATTACAGGTACAAGCCATGGCACCTG TCCAGTGATCCTCCTGCTTCAGCCTCCTGAGTGGCTGTGATTACAGGTACAAGCCATGGCACCTG T C AC125611.4 Ensembl:ENSG00000258334 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49324210..49324282 26863196 MeRIP-seq:(Medium) rs1380244503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1364492 85620 RMVar_ID_85620 Human_SNP_ID_500569760 m1A Human chr12 - 49330076 49330076 49330076 ATGTGCGTTCAGTAGTCTACCCACACTGTCCTATTCCTGATCCCCCATCTCTTTTCCCTCTTCCT ATGTGCGTTCAGTAGTCTACCCACACTGTCCTGTTCCTGATCCCCCATCTCTTTTCCCTCTTCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49330026..49330144 26863196 MeRIP-seq:(Medium) rs925751408 Functional Loss SNV dbSNP153 33..33 33 - - - 85621 RMVar_ID_85621 Human_SNP_ID_500570197 m1A Human chr12 + 49331195 49331195 49331195 GGTGGAAGTATAGGACCCCAGACCTCCCTCTAAATTTTCCATGCCCCTCAGGCCTCAGCAATCTG GGTGGAAGTATAGGACCCCAGACCTCCCTCTATATTTTCCATGCCCCTCAGGCCTCAGCAATCTG A T TROAP Ensembl:ENSG00000135451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49331167..49331309 26863196 MeRIP-seq:(Medium) rs1351330541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34775,Human_RBP_ID_874523,Human_RBP_ID_18160190,Human_RBP_ID_19703240,Human_RBP_ID_22644780,Human_RBP_ID_27422415 RMVar_hsa_circ_91573,RMVar_hsa_circ_156322,RMVar_hsa_circ_87814,RMVar_hsa_circ_156325 85622 RMVar_ID_85622 Human_SNP_ID_500570212 m1A Human chr12 + 49331253 49331253 49331253 CAATCTGGCCCCTCGAACCCTAGCCCTGAGGGAGCGCCTCAAATCGTGTTTAACCGCCATCCACT CAATCTGGCCCCTCGAACCCTAGCCCTGAGGGTGCGCCTCAAATCGTGTTTAACCGCCATCCACT A T TROAP Ensembl:ENSG00000135451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49331207..49331407 26863196 MeRIP-seq:(Medium) rs1365284665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420918,Human_RBP_ID_18160027,Human_RBP_ID_18627697 Human_Splice_Rec_1364644,Human_Splice_Rec_1364756 RMVar_hsa_circ_91573,RMVar_hsa_circ_156322,RMVar_hsa_circ_87814,RMVar_hsa_circ_114566,RMVar_hsa_circ_156325,RMVar_hsa_circ_156326 85623 RMVar_ID_85623 Human_SNP_ID_500570651 m1A Human chr12 - 49332797 49332796 49332797 TCACCCGCACCCAAGTGCGCGCTGGACCCCATAGGGGCAGAGGTCGTGGCTTTCTCTTTTGTACA TCACCCGCACCCAAGTGCGCGCTGGACCCCAT_GGGGCAGAGGTCGTGGCTTTCTCTTTTGTACA CT C C1QL4 Ensembl:ENSG00000186897 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49332509..49332805 32194978 MeRIP-seq:(Medium) rs1277544223 Functional Loss DEL dbSNP153 33..33 33 - - - 85624 RMVar_ID_85624 Human_SNP_ID_500571977 m1A Human chr12 - 49336941 49336941 49336941 GAGCGCGGGGAGCAGTCCCCTCTCCATCAGGGAGTGGTCTATCTGGGCAGTCTGGGACCCAGGCA GAGCGCGGGGAGCAGTCCCCTCTCCATCAGGGGGTGGTCTATCTGGGCAGTCTGGGACCCAGGCA T C C1QL4 Ensembl:ENSG00000186897 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49336891..49336991 32194978 MeRIP-seq:(Medium) rs1232311240 Functional Loss SNV dbSNP153 33..33 33 - - - 85625 RMVar_ID_85625 Human_SNP_ID_500587852 m1A Human chr12 - 49400404 49400404 49400404 TTATCTCACTGAAAAAGATAAGCCATAACCCCAGTTTCCTCACCAGCTACTTATCCATTTCTCTG TTATCTCACTGAAAAAGATAAGCCATAACCCCGGTTTCCTCACCAGCTACTTATCCATTTCTCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49400403..49400481 26863196 MeRIP-seq:(Medium) rs1206791206 Functional Loss SNV dbSNP153 33..33 33 - - - 85626 RMVar_ID_85626 Human_SNP_ID_500618626 m1A Human chr12 - 49526116 49526116 49526116 TGGTCCCTGCAGAGTGAGTCTGGCCTCTTTCAATGGTGTTTCCTGGTGCCTGAGATGGAGCACTC TGGTCCCTGCAGAGTGAGTCTGGCCTCTTTCAGTGGTGTTTCCTGGTGCCTGAGATGGAGCACTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49526065..49526244 26863196 MeRIP-seq:(Medium) rs145898849 Functional Loss SNV dbSNP153 33..33 33 - - - 85627 RMVar_ID_85627 Human_SNP_ID_500627698 m1A Human chr12 - 49558873 49558873 49558873 ATCGATGGACGGCCGGTGCTCTGTGGCTCCAAATGGCGCCTCAGCAACAACTCTGTGGTGGAGGT ATCGATGGACGGCCGGTGCTCTGTGGCTCCAAGTGGCGCCTCAGCAACAACTCTGTGGTGGAGGT T C MCRS1 Ensembl:ENSG00000187778 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49558681..49558944 32194978 MeRIP-seq:(Medium) rs767081667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421005,Human_RBP_ID_8782373,Human_RBP_ID_19056118,Human_RBP_ID_27422453 Human_Splice_Rec_1365096,Human_Splice_Rec_1365097,Human_Splice_Rec_1365120,Human_Splice_Rec_1365121,Human_Splice_Rec_1365148,Human_Splice_Rec_1365149,Human_Splice_Rec_1365172,Human_Splice_Rec_1365173,Human_Splice_Rec_1365198,Human_Splice_Rec_1365199,Human_Splice_Rec_1365228,Human_Splice_Rec_1365229,Human_Splice_Rec_1365231,Human_Splice_Rec_1365238,Human_Splice_Rec_1365239,Human_Splice_Rec_1365252,Human_Splice_Rec_1365253,Human_Splice_Rec_1365278,Human_Splice_Rec_1365279 RMVar_hsa_circ_25652,RMVar_hsa_circ_156347,RMVar_hsa_circ_89336,RMVar_hsa_circ_114943,RMVar_hsa_circ_93318,RMVar_hsa_circ_83043,RMVar_hsa_circ_156348,RMVar_hsa_circ_156345,RMVar_hsa_circ_156346,RMVar_hsa_circ_107289,RMVar_hsa_circ_156349 85628 RMVar_ID_85628 Human_SNP_ID_500629846 m1A Human chr12 - 49566152 49566152 49566152 GGCATCAGGCACTGCCAGCCGCTCAGAGGATGAGGAGTCACTGGCAGGGCAGAAGCGAGCCTCCT GGCATCAGGCACTGCCAGCCGCTCAGAGGATGTGGAGTCACTGGCAGGGCAGAAGCGAGCCTCCT T A MCRS1 Ensembl:ENSG00000187778 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49566101..49566267 26863196 MeRIP-seq:(Medium) rs1180028767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421019,Human_RBP_ID_8377397,Human_RBP_ID_23562215 Human_Splice_Rec_1365126,Human_Splice_Rec_1365127,Human_Splice_Rec_1365177,Human_Splice_Rec_1365206,Human_Splice_Rec_1365207,Human_Splice_Rec_1365256,Human_Splice_Rec_1365257,Human_Splice_Rec_1365284,Human_Splice_Rec_1365285,Human_Splice_Rec_1365304,Human_Splice_Rec_1365305,Human_Splice_Rec_1365316,Human_Splice_Rec_1365317,Human_Splice_Rec_1365326,Human_Splice_Rec_1365327,Human_Splice_Rec_1365333 RMVar_hsa_circ_120368,RMVar_hsa_circ_156351,RMVar_hsa_circ_156352,RMVar_hsa_circ_117931 85629 RMVar_ID_85629 Human_SNP_ID_500630425 m1A Human chr12 - 49568078 49568078 49568078 CTTTGGCCCTGCGGCTGCTACCGTCGCCGCGGAGAAATTGTTGGATCTGGCAGTCTAGGAATGGT CTTTGGCCCTGCGGCTGCTACCGTCGCCGCGGGGAAATTGTTGGATCTGGCAGTCTAGGAATGGT T C MCRS1 Ensembl:ENSG00000187778 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49567995..49568083 26863196 MeRIP-seq:(Medium) rs926182998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421025,Human_RBP_ID_1472731,Human_RBP_ID_4246637,Human_RBP_ID_8377402,Human_RBP_ID_18417265,Human_RBP_ID_23562217 Human_Splice_Rec_1365099,Human_Splice_Rec_1365123,Human_Splice_Rec_1365151,Human_Splice_Rec_1365201,Human_Splice_Rec_1365281,Human_Splice_Rec_1365283,Human_Splice_Rec_1365331 85630 RMVar_ID_85630 Human_SNP_ID_500630515 m1A Human chr12 - 49568277 49568277 49568277 TCTCCGGTGCCTATAATCCTTAACGTTTCCCTATATGCTGTCCCAACTAGGAAAGCCTTTACTTT TCTCCGGTGCCTATAATCCTTAACGTTTCCCTGTATGCTGTCCCAACTAGGAAAGCCTTTACTTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49568229..49568640 26863196 MeRIP-seq:(Medium) rs1285980212 Functional Loss SNV dbSNP153 33..33 33 - - - 85631 RMVar_ID_85631 Human_SNP_ID_500631342 m1A Human chr12 + 49572053 49572053 49572053 GAGATATCCACTGGGGAGTCATCATCAGGAAGATCTGGATGTGGATGCTTAAGGAGAGAGTGTGG GAGATATCCACTGGGGAGTCATCATCAGGAAGGTCTGGATGTGGATGCTTAAGGAGAGAGTGTGG A G PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49572012..49572111 26863196 MeRIP-seq:(Medium) rs187775435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6191343,Human_RBP_ID_11957622 85632 RMVar_ID_85632 Human_SNP_ID_500632911 m1A Human chr12 + 49579447 49579447 49579447 CATGATGTCACTTCTCTGCTTAGAATTCTGCAATGGCTCCCATTGCATTCCGGGTGAACAGAGGT CATGATGTCACTTCTCTGCTTAGAATTCTGCAGTGGCTCCCATTGCATTCCGGGTGAACAGAGGT A G PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49579430..49579525 26863196 MeRIP-seq:(Medium) rs1181139119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11957771 85633 RMVar_ID_85633 Human_SNP_ID_500643041 m1A Human chr12 - 49622884 49622884 49622884 TGTGAGGTACATGCTTGCTGTGCGGCTGAGGAAACTGTAACCTGGAGCTCTGCGGGGAATGCGCT TGTGAGGTACATGCTTGCTGTGCGGCTGAGGAGACTGTAACCTGGAGCTCTGCGGGGAATGCGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49622775..49622887 26863196 MeRIP-seq:(Medium) rs1025173984 Functional Loss SNV dbSNP153 33..33 33 - - - 85634 RMVar_ID_85634 Human_SNP_ID_500643255 m1A Human chr12 + 49623491 49623491 49623491 AGCCACCGGAGCCCCGGCCACGAAGGGGTGCGACCCCCCGCCGGCCCCGCCCTCCCGGCTGCGGC AGCCACCGGAGCCCCGGCCACGAAGGGGTGCGCCCCCCCGCCGGCCCCGCCCTCCCGGCTGCGGC A C PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:49623453..49623537 26863410 MeRIP-seq:(Medium) rs866111935 Functional Loss SNV dbSNP153 33..33 33 - - - 85635 RMVar_ID_85635 Human_SNP_ID_500643324 m1A Human chr12 + 49623718 49623718 49623718 GGGGATAGCTGGGACCCCGGGGAGGGCGAGGGAGGCCAAGGGTGAGGGAAGAGAGCCCGGGAGGG GGGGATAGCTGGGACCCCGGGGAGGGCGAGGGCGGCCAAGGGTGAGGGAAGAGAGCCCGGGAGGG A C PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49623454..49623743 26863196 MeRIP-seq:(Medium) rs1243207070 Functional Loss SNV dbSNP153 33..33 33 - - - 85636 RMVar_ID_85636 Human_SNP_ID_500643473 m1A Human chr12 - 49624294 49624294 49624294 TTCCTTTGCTTCCCTACCAAACCCATTCTCCTAAACTTCCTCCTCAAAAACCTATTCATTTAGAC TTCCTTTGCTTCCCTACCAAACCCATTCTCCTGAACTTCCTCCTCAAAAACCTATTCATTTAGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49624286..49624532 26863196 MeRIP-seq:(Medium) rs1294421178 Functional Loss SNV dbSNP153 33..33 33 - - - 85637 RMVar_ID_85637 Human_SNP_ID_500644596 m1A Human chr12 + 49629880 49629880 49629880 CAAAGCCTACATCCACAGGGAGATAGTTCAGGATTTGTAGAGGAGGGGATGGACACCAAAAAGGG CAAAGCCTACATCCACAGGGAGATAGTTCAGGCTTTGTAGAGGAGGGGATGGACACCAAAAAGGG A C PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49629873..49630056 26863196 MeRIP-seq:(Medium) rs1047480417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6191438,Human_RBP_ID_11958073 85638 RMVar_ID_85638 Human_SNP_ID_500646759 m1A Human chr12 - 49637366 49637366 49637366 GGGAATGGCAGAGGAAGAGGCAGGGACAATCAAGATTGAGGAAATGCAGGCAAGAGAGGCAGAGA GGGAATGGCAGAGGAAGAGGCAGGGACAATCACGATTGAGGAAATGCAGGCAAGAGAGGCAGAGA T G FMNL3 Ensembl:ENSG00000161791 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49637256..49637440 26863196 MeRIP-seq:(Medium) rs1170817401 Functional Loss SNV dbSNP153 33..33 33 - - - 85639 RMVar_ID_85639 Human_SNP_ID_500648494 m1A Human chr12 + 49643881 49643881 49643881 GGACTCTTACAGAATAGTCCTGAGAGTGAGACAGACCCTGAGGAGAAAGCTGGCAAGGAGAGCGA GGACTCTTACAGAATAGTCCTGAGAGTGAGACGGACCCTGAGGAGAAAGCTGGCAAGGAGAGCGA A G PRPF40B Ensembl:ENSG00000110844 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49643871..49643971 32194978 MeRIP-seq:(Medium) rs1204354224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1365402,Human_Splice_Rec_1365464,Human_Splice_Rec_1365524,Human_Splice_Rec_1365550 85640 RMVar_ID_85640 Human_SNP_ID_500650887 m1A Human chr12 - 49652197 49652197 49652197 TGCTGTCTGCCTGCCAGGAGACATATGAGAACACAAGCCACCAGGTGCACACCCTGCGGAGGCTC TGCTGTCTGCCTGCCAGGAGACATATGAGAACGCAAGCCACCAGGTGCACACCCTGCGGAGGCTC T C FMNL3 Ensembl:ENSG00000161791 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49651982..49652249 26863196 MeRIP-seq:(Medium) rs1184093076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1365632,Human_Splice_Rec_1365682,Human_Splice_Rec_1365752 RMVar_hsa_circ_31844,RMVar_hsa_circ_28763,RMVar_hsa_circ_126265,RMVar_hsa_circ_82280,RMVar_hsa_circ_156357,RMVar_hsa_circ_156358 85641 RMVar_ID_85641 Human_SNP_ID_500675130 m1A Human chr12 - 49752980 49752980 49752980 TGCATAGACCTTCTTCAGGTGCTGCTGCGTTGACGGGGTTCTAAGAAAAGAATGTGAATAAGAGC TGCATAGACCTTCTTCAGGTGCTGCTGCGTTGGCGGGGTTCTAAGAAAAGAATGTGAATAAGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49752951..49753000 26863196 MeRIP-seq:(Medium) rs1425356544 Functional Loss SNV dbSNP153 33..33 33 - - - 85642 RMVar_ID_85642 Human_SNP_ID_500678175 m1A Human chr12 + 49763125 49763125 49763125 TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCAACCCCATCTGTAGCCTCTTCCTCTACTCAGGCA TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCACCCCCATCTGTAGCCTCTTCCTCTACTCAGGCA A C TMBIM6 Ensembl:ENSG00000139644 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49763076..49763125 26863196 MeRIP-seq:(Medium) rs74087196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269472,Human_RBP_ID_421080,Human_RBP_ID_1083022,Human_RBP_ID_1167052,Human_RBP_ID_1357710,Human_RBP_ID_1472799,Human_RBP_ID_1796193,Human_RBP_ID_2340699,Human_RBP_ID_3407208,Human_RBP_ID_4225776,Human_RBP_ID_6191737,Human_RBP_ID_8068354,Human_RBP_ID_8177894,Human_RBP_ID_8377505,Human_RBP_ID_11958940,Human_RBP_ID_17238788,Human_RBP_ID_17354574,Human_RBP_ID_17471625,Human_RBP_ID_17820682,Human_RBP_ID_18206345,Human_RBP_ID_18627870,Human_RBP_ID_18935236,Human_RBP_ID_19775946,Human_RBP_ID_22383294,Human_RBP_ID_22794297,Human_RBP_ID_22904704,Human_RBP_ID_23157703,Human_RBP_ID_23562356,Human_RBP_ID_24407208,Human_RBP_ID_24466552,Human_RBP_ID_24975166,Human_RBP_ID_26416492,Human_RBP_ID_26907317,Human_RBP_ID_27215020,Human_RBP_ID_27422480 Human_miRNA_ID_1531690 RMVar_hsa_circ_123454,RMVar_hsa_circ_156369,RMVar_hsa_circ_156372,RMVar_hsa_circ_125329 85643 RMVar_ID_85643 Human_SNP_ID_500678176 m1A Human chr12 + 49763125 49763125 49763125 TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCAACCCCATCTGTAGCCTCTTCCTCTACTCAGGCA TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCAGCCCCATCTGTAGCCTCTTCCTCTACTCAGGCA A G TMBIM6 Ensembl:ENSG00000139644 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49763076..49763125 26863196 MeRIP-seq:(Medium) rs74087196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269472,Human_RBP_ID_421080,Human_RBP_ID_1083022,Human_RBP_ID_1167052,Human_RBP_ID_1357710,Human_RBP_ID_1472799,Human_RBP_ID_1796193,Human_RBP_ID_2340699,Human_RBP_ID_3407208,Human_RBP_ID_4225776,Human_RBP_ID_6191737,Human_RBP_ID_8068354,Human_RBP_ID_8177894,Human_RBP_ID_8377505,Human_RBP_ID_11958940,Human_RBP_ID_17238788,Human_RBP_ID_17354574,Human_RBP_ID_17471625,Human_RBP_ID_17820682,Human_RBP_ID_18206345,Human_RBP_ID_18627870,Human_RBP_ID_18935236,Human_RBP_ID_19775946,Human_RBP_ID_22383294,Human_RBP_ID_22794297,Human_RBP_ID_22904704,Human_RBP_ID_23157703,Human_RBP_ID_23562356,Human_RBP_ID_24407208,Human_RBP_ID_24466552,Human_RBP_ID_24975166,Human_RBP_ID_26416492,Human_RBP_ID_26907317,Human_RBP_ID_27215020,Human_RBP_ID_27422480 Human_miRNA_ID_1531690 RMVar_hsa_circ_123454,RMVar_hsa_circ_156369,RMVar_hsa_circ_156372,RMVar_hsa_circ_125329 85644 RMVar_ID_85644 Human_SNP_ID_500678544 m1A Human chr12 - 49764401 49764401 49764401 CAACTTAGAAACAAATGATTTCGTAGGATAGCACAGTGACATGGTGCACTGTGAACCTGAGGCCA CAACTTAGAAACAAATGATTTCGTAGGATAGCTCAGTGACATGGTGCACTGTGAACCTGAGGCCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49764376..49764400 32194978 MeRIP-seq:(Medium) rs895327908 Functional Loss SNV dbSNP153 33..33 33 - - - 85645 RMVar_ID_85645 Human_SNP_ID_500685348 m1A Human chr12 + 49791290 49791288 49791291 GGGGGCTGGGCCAGGCGCTTCAATATATAAAAACAACAACAAAAAAGACGGACGAACAGACCCCA GGGGGCTGGGCCAGGCGCTTCAATATATAAA___AACAACAAAAAAGACGGACGAACAGACCCCA AAAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49791239..49791444 32194978 MeRIP-seq:(Medium) rs1381198641 Functional Loss DEL dbSNP153 32..34 33 - - - 85646 RMVar_ID_85646 Human_SNP_ID_500685349 m1A Human chr12 + 49791290 49791290 49791290 GGGGGCTGGGCCAGGCGCTTCAATATATAAAAACAACAACAAAAAAGACGGACGAACAGACCCCA GGGGGCTGGGCCAGGCGCTTCAATATATAAAAGCAACAACAAAAAAGACGGACGAACAGACCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49791239..49791444 32194978 MeRIP-seq:(Medium) rs1488330649 Functional Loss SNV dbSNP153 33..33 33 - - - 85647 RMVar_ID_85647 Human_SNP_ID_500685784 m1A Human chr12 - 49792535 49792535 49792535 CCACCCCTCCTGTCCAGCTGGCCAAGAACTGGACCTTCCCCAATACTAGGGCAGCCGGCAGCTCC CCACCCCTCCTGTCCAGCTGGCCAAGAACTGGGCCTTCCCCAATACTAGGGCAGCCGGCAGCTCC T C NCKAP5L Ensembl:ENSG00000167566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49792413..49792536 26863196 MeRIP-seq:(Medium) rs1289159989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8782407,Human_RBP_ID_17238840,Human_RBP_ID_27422526 Human_Splice_Rec_1366072,Human_Splice_Rec_1366094,Human_Splice_Rec_1366095 85648 RMVar_ID_85648 Human_SNP_ID_500689109 m1A Human chr12 + 49803020 49803020 49803020 GTTGGCAACCTGGGGACAGAAAGCCCCGAGGCAGAGCCATCAGCTGACCCCAGCTTCTGCCAGGA GTTGGCAACCTGGGGACAGAAAGCCCCGAGGCGGAGCCATCAGCTGACCCCAGCTTCTGCCAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49803017..49803083 26863196 MeRIP-seq:(Medium) rs1254767038 Functional Loss SNV dbSNP153 33..33 33 - - - 85649 RMVar_ID_85649 Human_SNP_ID_500698613 m1A Human chr12 + 49843010 49843010 49843010 TAATGAGGAAAATTTCCGAACGGGGCGGCGCCAGGTGCCAGAACTCGCGATTCCTCTTCCGCTGC TAATGAGGAAAATTTCCGAACGGGGCGGCGCCCGGTGCCAGAACTCGCGATTCCTCTTCCGCTGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49842972..49843073 26863196 MeRIP-seq:(Medium) rs566100522 Functional Loss SNV dbSNP153 33..33 33 - - - 85650 RMVar_ID_85650 Human_SNP_ID_500729760 m1A Human chr12 + 49960639 49960639 49960639 AGGATGAGAGAAATGAATAGAGAGAGACAGAGAGACTAAGACAGCAAAAGGCAGGAAGGAAAAAC AGGATGAGAGAAATGAATAGAGAGAGACAGAGGGACTAAGACAGCAAAAGGCAGGAAGGAAAAAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49960450..49960945 26863196 MeRIP-seq:(Medium) rs549522958 Functional Loss SNV dbSNP153 33..33 33 - - - 85651 RMVar_ID_85651 Human_SNP_ID_500733429 m1A Human chr12 + 49973178 49973178 49973178 AGGCAAGGAACGGCCAAGGCACCAGGACATGGATGCAGTGGAGCCAGGGGGACGTGGCTGGGCCA AGGCAAGGAACGGCCAAGGCACCAGGACATGGTTGCAGTGGAGCCAGGGGGACGTGGCTGGGCCA A T AQP6 Ensembl:ENSG00000086159 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49973128..49973201 26863196 MeRIP-seq:(Medium) rs1282454403 Functional Loss SNV dbSNP153 33..33 33 - - - 85652 RMVar_ID_85652 Human_SNP_ID_515538918 m1A Human chr12 + 110019248 110019248 110019248 ATGGAGCGCCTCACTCTGGACTTGATGAAGCCAAAAAGCAGGGAAGTTGAGCGGCGGCTCACAAG ATGGAGCGCCTCACTCTGGACTTGATGAAGCCGAAAAGCAGGGAAGTTGAGCGGCGGCTCACAAG A G ANKRD13A Ensembl:ENSG00000076513 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110019201..110021131 32194978 MeRIP-seq:(Medium) rs890748209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33421,Human_RBP_ID_228494,Human_RBP_ID_410050,Human_RBP_ID_873269,Human_RBP_ID_2302243,Human_RBP_ID_4199881,Human_RBP_ID_9366924 Human_Splice_Rec_1422629,Human_Splice_Rec_1422651,Human_Splice_Rec_1422663,Human_Splice_Rec_1422683 RMVar_hsa_circ_7541,RMVar_hsa_circ_48664,RMVar_hsa_circ_273070,RMVar_hsa_circ_367147,RMVar_hsa_circ_325300,RMVar_hsa_circ_294879,RMVar_hsa_circ_50784,RMVar_hsa_circ_327722,RMVar_hsa_circ_159760,RMVar_hsa_circ_343494,RMVar_hsa_circ_305479,RMVar_hsa_circ_58387,RMVar_hsa_circ_159764,RMVar_hsa_circ_102007,RMVar_hsa_circ_159762,RMVar_hsa_circ_159763,RMVar_hsa_circ_331321,RMVar_hsa_circ_324122,RMVar_hsa_circ_159766,RMVar_hsa_circ_159767,RMVar_hsa_circ_159765,RMVar_hsa_circ_285963,RMVar_hsa_circ_297015,RMVar_hsa_circ_313634,RMVar_hsa_circ_324480,RMVar_hsa_circ_296568,RMVar_hsa_circ_122593,RMVar_hsa_circ_159768,RMVar_hsa_circ_159770,RMVar_hsa_circ_159771,RMVar_hsa_circ_159772,RMVar_hsa_circ_159769,RMVar_hsa_circ_12837,RMVar_hsa_circ_366957 85653 RMVar_ID_85653 Human_SNP_ID_515543145 m1A Human chr12 + 110038266 110038266 110038266 AATAGTTTCACATCACCTCACTGCACGCATCGAAGGATCTGATTTGAATTTGTAAAGGCAATTCT AATAGTTTCACATCACCTCACTGCACGCATCGGAGGATCTGATTTGAATTTGTAAAGGCAATTCT A G ANKRD13A Ensembl:ENSG00000076513 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110038262..110038713 32194978 MeRIP-seq:(Medium) rs1226568443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_410070,Human_RBP_ID_11801786,Human_RBP_ID_17467878,Human_RBP_ID_26421618 Human_miRNA_ID_1056885 RMVar_hsa_circ_159764,RMVar_hsa_circ_102007,RMVar_hsa_circ_122593,RMVar_hsa_circ_159772,RMVar_hsa_circ_159780,RMVar_hsa_circ_92455 85654 RMVar_ID_85654 Human_SNP_ID_515574906 m1A Human chr12 + 110172276 110172275 110172276 ACGTGATGAAACCCTGTCTCCACTAAAAATAGAAAAATTTGCCTCTGCCTCTGCCTCTGCCTCTG ACGTGATGAAACCCTGTCTCCACTAAAAATAG_AAAATTTGCCTCTGCCTCTGCCTCTGCCTCTG GA G IFT81 Ensembl:ENSG00000122970 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110172256..110172354 26863196 MeRIP-seq:(Medium) rs1566140911 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_159793,RMVar_hsa_circ_326158,RMVar_hsa_circ_339487,RMVar_hsa_circ_324390,RMVar_hsa_circ_314763,RMVar_hsa_circ_316535,RMVar_hsa_circ_159784,RMVar_hsa_circ_159785,RMVar_hsa_circ_159783,RMVar_hsa_circ_26565,RMVar_hsa_circ_48293,RMVar_hsa_circ_334095,RMVar_hsa_circ_342917,RMVar_hsa_circ_324233,RMVar_hsa_circ_14206,RMVar_hsa_circ_15104,RMVar_hsa_circ_159797,RMVar_hsa_circ_159795,RMVar_hsa_circ_159796,RMVar_hsa_circ_159794,RMVar_hsa_circ_4923,RMVar_hsa_circ_159792,RMVar_hsa_circ_18096,RMVar_hsa_circ_26653,RMVar_hsa_circ_265767,RMVar_hsa_circ_323000 85655 RMVar_ID_85655 Human_SNP_ID_515599752 m1A Human chr12 + 110281361 110281361 110281361 GGCGCTGAGGGACCCGGGCGAGCGCGCCGCGCACCGCCCCGCCGGCTCGCCTCCCTCGCCGCGTT GGCGCTGAGGGACCCGGGCGAGCGCGCCGCGCCCCGCCCCGCCGGCTCGCCTCCCTCGCCGCGTT A C ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEK293T,untreat control chr12:110281251..110281450;chr12:110281251..110281475;chr12:110281275..110281363 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1019728962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230103,Human_RBP_ID_4246297,Human_RBP_ID_5437238,Human_RBP_ID_6129202,Human_RBP_ID_9322680,Human_RBP_ID_22436679,Human_RBP_ID_22532439 85656 RMVar_ID_85656 Human_SNP_ID_515599758 m1A Human chr12 - 110281375 110281375 110281375 ACCACTGAGGGCGGAACGCGGCGAGGGAGGCGAGCCGGCGGGGCGGTGCGCGGCGCGCTCGCCCG ACCACTGAGGGCGGAACGCGGCGAGGGAGGCGGGCCGGCGGGGCGGTGCGCGGCGCGCTCGCCCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:110281256..110281457 32194978 MeRIP-seq:(Medium) rs1422054845 Functional Loss SNV dbSNP153 33..33 33 - - - 85657 RMVar_ID_85657 Human_SNP_ID_515599771 m1A Human chr12 - 110281404 110281404 110281404 CCCGGGCCGGAGGAGGGGGCGCCCGGCAGACCACTGAGGGCGGAACGCGGCGAGGGAGGCGAGCC CCCGGGCCGGAGGAGGGGGCGCCCGGCAGACCCCTGAGGGCGGAACGCGGCGAGGGAGGCGAGCC T G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr12:110281306..110281407 26863410 MeRIP-seq:(Medium) rs1271203279 Functional Loss SNV dbSNP153 33..33 33 - - - 85658 RMVar_ID_85658 Human_SNP_ID_515599889 m1A Human chr12 - 110281706 110281706 110281706 TCCGCCTCGCACTCCGGCCGCGGGCTCGTGCCACCCCGGGAGCCCAGGCGCGGACGGGCTCTCCC TCCGCCTCGCACTCCGGCCGCGGGCTCGTGCCCCCCCGGGAGCCCAGGCGCGGACGGGCTCTCCC T G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr12:110281606..110281807 26863410 MeRIP-seq:(Medium) rs1333494119 Functional Loss SNV dbSNP153 33..33 33 - - - 85659 RMVar_ID_85659 Human_SNP_ID_515599900 m1A Human chr12 + 110281732 110281732 110281732 CCGGGGTGGCACGAGCCCGCGGCCGGAGTGCGAGGCGGAGGCGAGGAGGCCGCGGGGACGGGAGG CCGGGGTGGCACGAGCCCGCGGCCGGAGTGCGTGGCGGAGGCGAGGAGGCCGCGGGGACGGGAGG A T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:110281251..110281925 26863196 MeRIP-seq:(Medium) rs1157966692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37049,Human_RBP_ID_230105,Human_RBP_ID_755048,Human_RBP_ID_3943406,Human_RBP_ID_4246304,Human_RBP_ID_5315046,Human_RBP_ID_5521696,Human_RBP_ID_8940726,Human_RBP_ID_9322686,Human_RBP_ID_22436685,Human_RBP_ID_22532516,Human_RBP_ID_26323351,Human_RBP_ID_26900616 85660 RMVar_ID_85660 Human_SNP_ID_515599908 m1A Human chr12 + 110281746 110281746 110281746 GCCCGCGGCCGGAGTGCGAGGCGGAGGCGAGGAGGCCGCGGGGACGGGAGGCGAGGCCGGCCGGG GCCCGCGGCCGGAGTGCGAGGCGGAGGCGAGGGGGCCGCGGGGACGGGAGGCGAGGCCGGCCGGG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:110281652..110281795 26863410 MeRIP-seq:(Medium) rs1472237478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37049,Human_RBP_ID_230105,Human_RBP_ID_755048,Human_RBP_ID_4200001,Human_RBP_ID_5315047,Human_RBP_ID_5521696,Human_RBP_ID_8940726,Human_RBP_ID_9322686,Human_RBP_ID_22436685,Human_RBP_ID_22472050,Human_RBP_ID_26323351 85661 RMVar_ID_85661 Human_SNP_ID_515599937 m1A Human chr12 + 110281811 110281811 110281811 CCCCCGAAGCCATGGAGAACGCGCACACCAAGACGGTGGAGGAGGTGCTGGGCCACTTCGGCGTC CCCCCGAAGCCATGGAGAACGCGCACACCAAGTCGGTGGAGGAGGTGCTGGGCCACTTCGGCGTC A T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110281251..110281925 26863196 MeRIP-seq:(Medium) rs753488422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4200002,Human_RBP_ID_6245225,Human_RBP_ID_8775724,Human_RBP_ID_8940726,Human_RBP_ID_9010685,Human_RBP_ID_9255586,Human_RBP_ID_23536504 Human_Splice_Rec_1422941,Human_Splice_Rec_1422979 85662 RMVar_ID_85662 Human_SNP_ID_515609694 m1A Human chr12 - 110316832 110316832 110316832 GTCACCCTCTCACCTCCCTCTGAGCATCACACACTATGCTCTTCAGTTCCTCTAACTTGTTTCTG GTCACCCTCTCACCTCCCTCTGAGCATCACACCCTATGCTCTTCAGTTCCTCTAACTTGTTTCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:110316830..110316948 26863196 MeRIP-seq:(Medium) rs774396362 Functional Loss SNV dbSNP153 33..33 33 - - - 85663 RMVar_ID_85663 Human_SNP_ID_515612128 m1A Human chr12 - 110326475 110326475 110326475 GTAAATAAAAACACATTTCATAAAGTACTTACAGAAAACAGCATGTTCTTTTTATCTTGGTTGAC GTAAATAAAAACACATTTCATAAAGTACTTACGGAAAACAGCATGTTCTTTTTATCTTGGTTGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110326450..110326523 26863196 MeRIP-seq:(Medium) rs1182164216 Functional Loss SNV dbSNP153 33..33 33 - - - 85664 RMVar_ID_85664 Human_SNP_ID_515617352 m1A Human chr12 + 110347044 110347044 110347044 TCCGTTCACCCCACCCCACCCCACCTCTCCCCACCTTACCCCCGCCCCGCTTGGCTTCTTCTTTA TCCGTTCACCCCACCCCACCCCACCTCTCCCCCCCTTACCCCCGCCCCGCTTGGCTTCTTCTTTA A C ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:110346944..110347195;chr12:110346994..110347179 32194978 MeRIP-seq:(Medium) rs938507310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229287,Human_RBP_ID_410222,Human_RBP_ID_754248,Human_RBP_ID_4249709,Human_RBP_ID_6129581,Human_RBP_ID_9661340,Human_RBP_ID_17475073,Human_RBP_ID_18934740,Human_RBP_ID_23536646,Human_RBP_ID_24406381,Human_RBP_ID_24463950 Human_miRNA_ID_446941,Human_miRNA_ID_450821,Human_miRNA_ID_842092,Human_miRNA_ID_1417992,Human_miRNA_ID_1701906,Human_miRNA_ID_2146813,Human_miRNA_ID_2367465,Human_miRNA_ID_2386948,Human_miRNA_ID_2388423,Human_miRNA_ID_2725970,Human_miRNA_ID_2988241,Human_miRNA_ID_3015260,Human_miRNA_ID_3021940,Human_miRNA_ID_3030627,Human_miRNA_ID_3065969 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_267949,RMVar_hsa_circ_100996,RMVar_hsa_circ_159835 85665 RMVar_ID_85665 Human_SNP_ID_515617841 m1A Human chr12 + 110348692 110348692 110348692 CAGGTACTCAAACCAGCCTGGGCAACAGAGTGAGGCCCTGTCAAAAAAAAATCAGCCTTACTGTG CAGGTACTCAAACCAGCCTGGGCAACAGAGTGGGGCCCTGTCAAAAAAAAATCAGCCTTACTGTG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:110348643..110348744 32194978 MeRIP-seq:(Medium) rs1397637295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2573808 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_267949,RMVar_hsa_circ_100996,RMVar_hsa_circ_159835 85666 RMVar_ID_85666 Human_SNP_ID_515617842 m1A Human chr12 + 110348692 110348692 110348692 CAGGTACTCAAACCAGCCTGGGCAACAGAGTGAGGCCCTGTCAAAAAAAAATCAGCCTTACTGTG CAGGTACTCAAACCAGCCTGGGCAACAGAGTGTGGCCCTGTCAAAAAAAAATCAGCCTTACTGTG A T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:110348643..110348744 32194978 MeRIP-seq:(Medium) rs1397637295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2573808 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_267949,RMVar_hsa_circ_100996,RMVar_hsa_circ_159835 85667 RMVar_ID_85667 Human_SNP_ID_515625195 m1A Human chr12 - 110376028 110376028 110376028 CACTAGCCTCCCTTGGGGGAAGGCCACTGAGGAGGGTAGAGGAGGCAGTGAGCTGTGTCACAGGA CACTAGCCTCCCTTGGGGGAAGGCCACTGAGGGGGGTAGAGGAGGCAGTGAGCTGTGTCACAGGA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110376006..110376087 26863196 MeRIP-seq:(Medium) rs1566257475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6129816,Human_RBP_ID_11805105,Human_RBP_ID_21919307 RMVar_hsa_circ_97652,RMVar_hsa_circ_159836 85668 RMVar_ID_85668 Human_SNP_ID_515628125 m1A Human chr12 - 110385278 110385274 110385278 AAGCGGGGGCTGCGGAGAGGCAGTGATTTTTTATTTGTTTGTTTGAGACGGAGTTTCACTCTTGT AAGCGGGGGCTGCGGAGAGGCAGTGATTTTTT____GTTTGTTTGAGACGGAGTTTCACTCTTGT CAAAT C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:110385261..110385406 26863196 MeRIP-seq:(Medium) rs1048636795 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6129927,Human_RBP_ID_11805485,Human_RBP_ID_23536796 RMVar_hsa_circ_94210,RMVar_hsa_circ_113675,RMVar_hsa_circ_97652,RMVar_hsa_circ_159836,RMVar_hsa_circ_348195,RMVar_hsa_circ_32018,RMVar_hsa_circ_159838,RMVar_hsa_circ_159839,RMVar_hsa_circ_60766,RMVar_hsa_circ_282619,RMVar_hsa_circ_337009,RMVar_hsa_circ_350663,RMVar_hsa_circ_313132,RMVar_hsa_circ_159842,RMVar_hsa_circ_159844,RMVar_hsa_circ_159843,RMVar_hsa_circ_159848,RMVar_hsa_circ_341416,RMVar_hsa_circ_159841,RMVar_hsa_circ_271397 85669 RMVar_ID_85669 Human_SNP_ID_515628127 m1A Human chr12 - 110385278 110385278 110385278 AAGCGGGGGCTGCGGAGAGGCAGTGATTTTTTATTTGTTTGTTTGAGACGGAGTTTCACTCTTGT AAGCGGGGGCTGCGGAGAGGCAGTGATTTTTTGTTTGTTTGTTTGAGACGGAGTTTCACTCTTGT T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:110385261..110385406 26863196 MeRIP-seq:(Medium) rs1313330660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6129927,Human_RBP_ID_11805485,Human_RBP_ID_23536796 RMVar_hsa_circ_94210,RMVar_hsa_circ_113675,RMVar_hsa_circ_97652,RMVar_hsa_circ_159836,RMVar_hsa_circ_348195,RMVar_hsa_circ_32018,RMVar_hsa_circ_159838,RMVar_hsa_circ_159839,RMVar_hsa_circ_60766,RMVar_hsa_circ_282619,RMVar_hsa_circ_337009,RMVar_hsa_circ_350663,RMVar_hsa_circ_313132,RMVar_hsa_circ_159842,RMVar_hsa_circ_159844,RMVar_hsa_circ_159843,RMVar_hsa_circ_159848,RMVar_hsa_circ_341416,RMVar_hsa_circ_159841,RMVar_hsa_circ_271397 85670 RMVar_ID_85670 Human_SNP_ID_515640272 m1A Human chr12 + 110429305 110429305 110429305 TGCGGCCACAGTGAAGAGGGAGTAGGGGACTCACCCCTCCTGCCTTCCTGTAGCCGAAGGGGGCT TGCGGCCACAGTGAAGAGGGAGTAGGGGACTCCCCCCTCCTGCCTTCCTGTAGCCGAAGGGGGCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:110429276..110429350 32194978 MeRIP-seq:(Medium) rs1033284284 Functional Loss SNV dbSNP153 33..33 33 - - - 85671 RMVar_ID_85671 Human_SNP_ID_515642211 m1A Human chr12 - 110435178 110435177 110435178 CTTGCTTTGTGAAGAGACAGTTCATGAACAAGAGTCTTTCAGGACCTGGACAGTGAAGGGAGCCC CTTGCTTTGTGAAGAGACAGTTCATGAACAAG_GTCTTTCAGGACCTGGACAGTGAAGGGAGCCC CT C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs753018601 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_410350,Human_RBP_ID_3421375,Human_RBP_ID_11806485,Human_RBP_ID_22436694,Human_RBP_ID_23208224 Human_Splice_Rec_1423208,Human_Splice_Rec_1423212 85672 RMVar_ID_85672 Human_SNP_ID_515642622 m1A Human chr12 + 110436609 110436609 110436609 GGTTTGGCATAAATTGCGTTAAGTGGAAAACCAGGCTCTCCAGGAATGGGAAAATTAGTGATTCC GGTTTGGCATAAATTGCGTTAAGTGGAAAACCGGGCTCTCCAGGAATGGGAAAATTAGTGATTCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110436551..110436700 32194978 MeRIP-seq:(Medium) rs766886826 Functional Loss SNV dbSNP153 33..33 33 - - - 85673 RMVar_ID_85673 Human_SNP_ID_515645115 m1A Human chr12 + 110445496 110445496 110445496 CAGGTCCTTTGAATTGACTTCTGATAGGCAACAGTGCCATGTTTCCGATGAGTTTGGTATCAGGA CAGGTCCTTTGAATTGACTTCTGATAGGCAACTGTGCCATGTTTCCGATGAGTTTGGTATCAGGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:110445451..110445525 26863196 MeRIP-seq:(Medium) rs768969588 Functional Loss SNV dbSNP153 33..33 33 - - - 85674 RMVar_ID_85674 Human_SNP_ID_515648513 m1A Human chr12 - 110458893 110458893 110458893 TAAGGCACTGAAAAGGCCAGTGTGGCTGGAGCATAATAAACAAAGAGGCAATTGTCATGAGGTGT TAAGGCACTGAAAAGGCCAGTGTGGCTGGAGCGTAATAAACAAAGAGGCAATTGTCATGAGGTGT T C GPN3 Ensembl:ENSG00000111231 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110458889..110459034 26863196 MeRIP-seq:(Medium) rs1465702059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806756 RMVar_hsa_circ_10946,RMVar_hsa_circ_318080,RMVar_hsa_circ_159861 85675 RMVar_ID_85675 Human_SNP_ID_515650072 m1A Human chr12 - 110465199 110465199 110465199 GCCTTGTGACATTACAGAGCACCTACTGTGCCACCATGGTCCAGCACTGTGAAGCCCTCAACCGG GCCTTGTGACATTACAGAGCACCTACTGTGCCTCCATGGTCCAGCACTGTGAAGCCCTCAACCGG T A GPN3 Ensembl:ENSG00000111231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110465151..110465252 26863196 MeRIP-seq:(Medium) rs199875960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1355984,Human_RBP_ID_4200496,Human_RBP_ID_5315048,Human_RBP_ID_9279206,Human_RBP_ID_22438030 Human_Splice_Rec_1423246,Human_Splice_Rec_1423247,Human_Splice_Rec_1423260,Human_Splice_Rec_1423261,Human_Splice_Rec_1423274,Human_Splice_Rec_1423275,Human_Splice_Rec_1423298,Human_Splice_Rec_1423299,Human_Splice_Rec_1423308,Human_Splice_Rec_1423309,Human_Splice_Rec_1423312,Human_Splice_Rec_1423316 85676 RMVar_ID_85676 Human_SNP_ID_515650073 m1A Human chr12 - 110465199 110465199 110465199 GCCTTGTGACATTACAGAGCACCTACTGTGCCACCATGGTCCAGCACTGTGAAGCCCTCAACCGG GCCTTGTGACATTACAGAGCACCTACTGTGCCGCCATGGTCCAGCACTGTGAAGCCCTCAACCGG T C GPN3 Ensembl:ENSG00000111231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110465151..110465252 26863196 MeRIP-seq:(Medium) rs199875960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1355984,Human_RBP_ID_4200496,Human_RBP_ID_5315048,Human_RBP_ID_9279206,Human_RBP_ID_22438030 Human_Splice_Rec_1423246,Human_Splice_Rec_1423247,Human_Splice_Rec_1423260,Human_Splice_Rec_1423261,Human_Splice_Rec_1423274,Human_Splice_Rec_1423275,Human_Splice_Rec_1423298,Human_Splice_Rec_1423299,Human_Splice_Rec_1423308,Human_Splice_Rec_1423309,Human_Splice_Rec_1423312,Human_Splice_Rec_1423316 85677 RMVar_ID_85677 Human_SNP_ID_515650820 m1A Human chr12 - 110468210 110468210 110468210 AAGGCTAAGGGAGTGTGGCGGGCGGCTCCGGGAGCCAACATGCCTCGGTATGCGCAGCTGGTCAT AAGGCTAAGGGAGTGTGGCGGGCGGCTCCGGGGGCCAACATGCCTCGGTATGCGCAGCTGGTCAT T C GPN3 Ensembl:ENSG00000111231 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110468097..110468250 26863196 MeRIP-seq:(Medium) rs537105879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246983,Human_RBP_ID_5314658,Human_RBP_ID_9322691,Human_RBP_ID_22438031,Human_RBP_ID_26321991 Human_Splice_Rec_1423245,Human_Splice_Rec_1423273,Human_Splice_Rec_1423297,Human_Splice_Rec_1423311,Human_Splice_Rec_1423315 85678 RMVar_ID_85678 Human_SNP_ID_515651081 m1A Human chr12 + 110468900 110468900 110468900 GGGGAGGGATGCTGGGACAGCTGCTCCCGCACACGGCTCGCGGTCTCGGCGCCGCGGAGATGCCC GGGGAGGGATGCTGGGACAGCTGCTCCCGCACTCGGCTCGCGGTCTCGGCGCCGCGGAGATGCCC A T FAM216A Ensembl:ENSG00000204856 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:110468851..110473111;chr12:110468851..110485150 26863196 MeRIP-seq:(Medium) rs1288780405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229517,Human_RBP_ID_410386,Human_RBP_ID_4200524 Human_miRNA_ID_2077108 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 85679 RMVar_ID_85679 Human_SNP_ID_515655521 m1A Human chr12 - 110486589 110486582 110486590 TCCAGTTGATGTCGCCATGTAGTGCAAGGGTAATGCTGTTTCTGTGAGTAACGGGAGCTAAGGCG TCCAGTTGATGTCGCCATGTAGTGCAAGGGT________TTCTGTGAGTAACGGGAGCTAAGGCG AACAGCATT A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:110486459..110486629 26863196 MeRIP-seq:(Medium) rs1332215754 Functional Loss DEL dbSNP153 32..39 33 - - - 85680 RMVar_ID_85680 Human_SNP_ID_515655522 m1A Human chr12 - 110486589 110486589 110486589 TCCAGTTGATGTCGCCATGTAGTGCAAGGGTAATGCTGTTTCTGTGAGTAACGGGAGCTAAGGCG TCCAGTTGATGTCGCCATGTAGTGCAAGGGTAGTGCTGTTTCTGTGAGTAACGGGAGCTAAGGCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:110486459..110486629 26863196 MeRIP-seq:(Medium) rs770837675 Functional Loss SNV dbSNP153 33..33 33 - - - 85681 RMVar_ID_85681 Human_SNP_ID_515655554 m1A Human chr12 + 110486677 110486677 110486677 ATATCGCAGCTGCATCTGCACCTGAAATGCTCATACAGCATTCCCTTTGGCGGCCAGTGAGAAAC ATATCGCAGCTGCATCTGCACCTGAAATGCTCCTACAGCATTCCCTTTGGCGGCCAGTGAGAAAC A C FAM216A Ensembl:ENSG00000204856 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110486589..110486688 32194978 MeRIP-seq:(Medium) rs368343004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_989609,Human_RBP_ID_27805986 Human_Splice_Rec_1423343,Human_Splice_Rec_1423349 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783,RMVar_hsa_circ_329080,RMVar_hsa_circ_344126,RMVar_hsa_circ_32909,RMVar_hsa_circ_159865,RMVar_hsa_circ_280520,RMVar_hsa_circ_283953,RMVar_hsa_circ_159866,RMVar_hsa_circ_159864,RMVar_hsa_circ_98906,RMVar_hsa_circ_159867 85682 RMVar_ID_85682 Human_SNP_ID_515655555 m1A Human chr12 + 110486677 110486677 110486677 ATATCGCAGCTGCATCTGCACCTGAAATGCTCATACAGCATTCCCTTTGGCGGCCAGTGAGAAAC ATATCGCAGCTGCATCTGCACCTGAAATGCTCGTACAGCATTCCCTTTGGCGGCCAGTGAGAAAC A G FAM216A Ensembl:ENSG00000204856 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110486589..110486688 32194978 MeRIP-seq:(Medium) rs368343004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_989609,Human_RBP_ID_27805986 Human_Splice_Rec_1423343,Human_Splice_Rec_1423349 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783,RMVar_hsa_circ_329080,RMVar_hsa_circ_344126,RMVar_hsa_circ_32909,RMVar_hsa_circ_159865,RMVar_hsa_circ_280520,RMVar_hsa_circ_283953,RMVar_hsa_circ_159866,RMVar_hsa_circ_159864,RMVar_hsa_circ_98906,RMVar_hsa_circ_159867 85683 RMVar_ID_85683 Human_SNP_ID_515659348 m1A Human chr12 - 110501911 110501911 110501911 CCTCGGCGTCAGGGCCCAGGCGCTGGCCTGGGAAAGGCCCAGAAGAGGTCTAGGGAAGGAAGGGA CCTCGGCGTCAGGGCCCAGGCGCTGGCCTGGGGAAGGCCCAGAAGAGGTCTAGGGAAGGAAGGGA T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:110501902..110502028 26863196 MeRIP-seq:(Medium) rs1244635039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5348724,Human_RBP_ID_9416169,Human_RBP_ID_21919076 85684 RMVar_ID_85684 Human_SNP_ID_515675644 m1A Human chr12 + 110567464 110567464 110567464 TTCCTTTTGCATTTCCCACCCTAATTAATGGCAGCCCAGCTACCCATACATACTTCCAGGCTTAG TTCCTTTTGCATTTCCCACCCTAATTAATGGCGGCCCAGCTACCCATACATACTTCCAGGCTTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110567459..110567550 26863196 MeRIP-seq:(Medium) rs969697097 Functional Loss SNV dbSNP153 33..33 33 - - - 85685 RMVar_ID_85685 Human_SNP_ID_515679820 m1A Human chr12 + 110583054 110583054 110583054 CCGAGAACATCGCCGCCGCCGCCCCCCCGAGGAGGCGGGGGGCCGGGGGAGCAGGAGGACGCGGA CCGAGAACATCGCCGCCGCCGCCCCCCCGAGGCGGCGGGGGGCCGGGGGAGCAGGAGGACGCGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:110583018..110583149 32194978 MeRIP-seq:(Medium) rs1257933047 Functional Loss SNV dbSNP153 33..33 33 - - - 85686 RMVar_ID_85686 Human_SNP_ID_515679829 m1A Human chr12 + 110583071 110583071 110583071 GCCGCCCCCCCGAGGAGGCGGGGGGCCGGGGGAGCAGGAGGACGCGGAGGCCCGGAGCCGGCTCT GCCGCCCCCCCGAGGAGGCGGGGGGCCGGGGGGGCAGGAGGACGCGGAGGCCCGGAGCCGGCTCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:110582970..110583270 26863410 MeRIP-seq:(Medium) rs978275953 Functional Loss SNV dbSNP153 33..33 33 - - - 85687 RMVar_ID_85687 Human_SNP_ID_515695306 m1A Human chr12 + 110648833 110648833 110648833 TTTTATACAGTAGTTGTTTTATTTTATACAGTAGTTGTACAGTAATTGAGGAAAAATGTTGTCAG TTTTATACAGTAGTTGTTTTATTTTATACAGTGGTTGTACAGTAATTGAGGAAAAATGTTGTCAG A G TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:110648784..110648956 26863196 MeRIP-seq:(Medium) rs1413990535 Functional Loss SNV dbSNP153 33..33 33 - - - 85688 RMVar_ID_85688 Human_SNP_ID_515718043 m1A Human chr12 - 110742831 110742831 110742831 GAGGAAGTAGGGAGCGGGGTGGCAGGGGGGGGACCCGCCGCGGCTGCTGCCACCGCCGCCACCAC GAGGAAGTAGGGAGCGGGGTGGCAGGGGGGGGCCCCGCCGCGGCTGCTGCCACCGCCGCCACCAC T G PPP1CC Ensembl:ENSG00000186298 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:110742651..110742925;chr12:110742651..110742875;chr12:110742676..110742875;chr12:110742651..110742900;chr12:110734974..110742925;chr12:110742701..110742900 26863196 MeRIP-seq:(Medium) rs879027237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35861,Human_RBP_ID_229433,Human_RBP_ID_754428,Human_RBP_ID_811033,Human_RBP_ID_877588,Human_RBP_ID_4246309,Human_RBP_ID_5139704,Human_RBP_ID_5461375,Human_RBP_ID_8247469,Human_RBP_ID_8940728,Human_RBP_ID_9010921,Human_RBP_ID_9352773,Human_RBP_ID_9416173,Human_RBP_ID_17357352,Human_RBP_ID_18417336,Human_RBP_ID_23207846 RMVar_hsa_circ_82370,RMVar_hsa_circ_159902 85689 RMVar_ID_85689 Human_SNP_ID_515864790 m1A Human chr12 - 111361877 111361877 111361877 CTCCTTGACTGCATCCTTCAGTCTTGGCCCCTAGGCCTGGGGCCCCTTGGGAGCTTGCCTGACCT CTCCTTGACTGCATCCTTCAGTCTTGGCCCCTGGGCCTGGGGCCCCTTGGGAGCTTGCCTGACCT T C PHETA1 Ensembl:ENSG00000198324 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs874286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_109227,Human_miRNA_ID_836595 85690 RMVar_ID_85690 Human_SNP_ID_515864897 m1A Human chr12 - 111362255 111362255 111362255 AAGCAAATGCACAGTTAGTGCAGCTCCTGACCAGGCCTTCAGGGTGGACAGAGGGAGGATCGGTC AAGCAAATGCACAGTTAGTGCAGCTCCTGACCGGGCCTTCAGGGTGGACAGAGGGAGGATCGGTC T C PHETA1 Ensembl:ENSG00000198324 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10849938 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10201,GWAS_ID_10202,GWAS_ID_10203,GWAS_ID_10204 85691 RMVar_ID_85691 Human_SNP_ID_515878669 m1A Human chr12 + 111418387 111418387 111418387 CTTCCAGCGCTACTTCTGCCGCGAGGTGCGCGACGGACGGGCGCCGGGCCGCGACTACCGGGACA CTTCCAGCGCTACTTCTGCCGCGAGGTGCGCGGCGGACGGGCGCCGGGCCGCGACTACCGGGACA A G SH2B3 Ensembl:ENSG00000111252 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:111418336..111434869 32194978 MeRIP-seq:(Medium) rs746394261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_878123,Human_RBP_ID_9322693,Human_RBP_ID_17809244 Human_miRNA_ID_1967303 RMVar_hsa_circ_84142,RMVar_hsa_circ_159934,RMVar_hsa_circ_93319,RMVar_hsa_circ_286281,RMVar_hsa_circ_159932,RMVar_hsa_circ_96434,RMVar_hsa_circ_159935,RMVar_hsa_circ_159933 85692 RMVar_ID_85692 Human_SNP_ID_515880505 m1A Human chr12 - 111425182 111425182 111425182 CACAGAGTGCTCTCTCCCAGCGCAGCCCTCATAGTGCCCCTGGAGGTGCTACACCATCACCCTGC CACAGAGTGCTCTCTCCCAGCGCAGCCCTCATGGTGCCCCTGGAGGTGCTACACCATCACCCTGC T C RF00017-1272 RNACentral:URS0000939112 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:111425179..111425270 26863196 MeRIP-seq:(Medium) rs867842518 Functional Loss SNV dbSNP153 33..33 33 - - - 85693 RMVar_ID_85693 Human_SNP_ID_515903914 m1A Human chr12 + 111516326 111516326 111516326 TTGGGACCTGACTGGTAGCGAGAAGGTGGGCGAGAGGAAGGAGATGGGCAAGGCGATGGCCAGGG TTGGGACCTGACTGGTAGCGAGAAGGTGGGCGGGAGGAAGGAGATGGGCAAGGCGATGGCCAGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:111516301..111516325 26863196 MeRIP-seq:(Medium) rs763579875 Functional Loss SNV dbSNP153 33..33 33 - - - 85694 RMVar_ID_85694 Human_SNP_ID_515904378 m1A Human chr12 + 111518651 111518650 111518651 CTTAGATTCTGCTCCTAAGCACAAAGTTTAACAGATGCGTGCTCATTCTCATCCCACTTGACCTC CTTAGATTCTGCTCCTAAGCACAAAGTTTAAC_GATGCGTGCTCATTCTCATCCCACTTGACCTC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:111518646..111518751 26863196 MeRIP-seq:(Medium) rs1566038444 Functional Loss DEL dbSNP153 33..33 33 - - - 85695 RMVar_ID_85695 Human_SNP_ID_515917475 m1A Human chr12 - 111570687 111570687 111570687 GCCATGGGTGGGCAGTGAAGAAAAAGGGCTTCAAAATAATGAGAGTTGAGATGGATCTTCAAGGA GCCATGGGTGGGCAGTGAAGAAAAAGGGCTTCGAAATAATGAGAGTTGAGATGGATCTTCAAGGA T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:111570638..111570775 26863196 MeRIP-seq:(Medium) rs1170480237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11813916 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 85696 RMVar_ID_85696 Human_SNP_ID_515925393 m1A Human chr12 - 111597795 111597795 111597795 AACCCCCGCCCCAATTTCGGAAATGCTAGGAGAGAGAGATTGCAGCAGGGGACGTGGTCGGGTTC AACCCCCGCCCCAATTTCGGAAATGCTAGGAGGGAGAGATTGCAGCAGGGGACGTGGTCGGGTTC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:111597743..111598035 26863196 MeRIP-seq:(Medium) rs1202326814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418473,Human_RBP_ID_11815033,Human_RBP_ID_18479648 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 85697 RMVar_ID_85697 Human_SNP_ID_515926321 m1A Human chr12 - 111599543 111599543 111599543 GGTAAAGAGTCCCTATCCGCACCTCCGCTCCCACCCGGCGCCTCGGCGCGCCCGCCCTCCGATGC GGTAAAGAGTCCCTATCCGCACCTCCGCTCCCCCCCGGCGCCTCGGCGCGCCCGCCCTCCGATGC T G ATXN2 Ensembl:ENSG00000204842 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:111599493..111599600 26863196 MeRIP-seq:(Medium) rs564109877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 85698 RMVar_ID_85698 Human_SNP_ID_515926376 m1A Human chr12 - 111599638 111599638 111599638 GAGAAAGCAACCCAGCGCGCCGCCCGCTCCTCACGTGTCCCTCCCGGCCCCGGGGCCACCTCACG GAGAAAGCAACCCAGCGCGCCGCCCGCTCCTCGCGTGTCCCTCCCGGCCCCGGGGCCACCTCACG T C ATXN2 Ensembl:ENSG00000204842 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:111599439..111599645 26863196 MeRIP-seq:(Medium) rs1181778524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1425073,Human_Splice_Rec_1425113 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 85699 RMVar_ID_85699 Human_SNP_ID_515948073 m1A Human chr12 - 111685804 111685804 111685804 CTCGCCTGAGCCCGCCGGGGCCCGCGCCGGCCAGCGCCTGCCCTATGAGTGTGTCACTGGTTGTT CTCGCCTGAGCCCGCCGGGGCCCGCGCCGGCCCGCGCCTGCCCTATGAGTGTGTCACTGGTTGTT T G BRAP Ensembl:ENSG00000089234 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:111685781..111685907 26863196 MeRIP-seq:(Medium) rs1426159803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246997,Human_RBP_ID_5437255,Human_RBP_ID_23538196,Human_RBP_ID_24366015 Human_Splice_Rec_1425403 85700 RMVar_ID_85700 Human_SNP_ID_515948235 m1A Human chr12 + 111686127 111686127 111686127 GACGTCGTGGAGATTGCTTGCGCTGGGGTGCCACACTTAGGCTGAGCTGCAGGTTTTCGCACAGT GACGTCGTGGAGATTGCTTGCGCTGGGGTGCCGCACTTAGGCTGAGCTGCAGGTTTTCGCACAGT A G ACAD10 Ensembl:ENSG00000111271 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:111686084..111686202 26863196 MeRIP-seq:(Medium) rs956054030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8365591,Human_RBP_ID_27807173 Human_miRNA_ID_2013112 RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 85701 RMVar_ID_85701 Human_SNP_ID_515948257 m1A Human chr12 + 111686186 111686186 111686186 CACAGTCGCGAGTTAACCTCTGCTTGCTCCAGAGGCCTCGTCCTAATCCACCTCGGCTGACGGCG CACAGTCGCGAGTTAACCTCTGCTTGCTCCAGTGGCCTCGTCCTAATCCACCTCGGCTGACGGCG A T ACAD10 Ensembl:ENSG00000111271 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:111686114..111686296 26863196 MeRIP-seq:(Medium) rs1463115917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1425461,Human_Splice_Rec_1425501,Human_Splice_Rec_1425503,Human_Splice_Rec_1425509,Human_Splice_Rec_1425517,Human_Splice_Rec_1425551,Human_Splice_Rec_1425575,Human_Splice_Rec_1425617,Human_Splice_Rec_1425625,Human_Splice_Rec_1425637 Human_miRNA_ID_2793069 RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 85702 RMVar_ID_85702 Human_SNP_ID_515958434 m1A Human chr12 + 111724795 111724772 111724796 CGGCATGAGAGGGAGACCGTGGAAAGAGAGGGAGGGGAGACCGTGGAAAGAGAGGGAGAGGGAGA CGGCATGAGA________________________GGGAGACCGTGGAAAGAGAGGGAGAGGGAGA AGGGAGACCGTGGAAAGAGAGGGAG A ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:111724760..111724939 26863196 MeRIP-seq:(Medium) rs1566155737 Functional Loss DEL dbSNP153 11..34 33 - - - RMVar_hsa_circ_87833,RMVar_hsa_circ_296193,RMVar_hsa_circ_317305,RMVar_hsa_circ_160020,RMVar_hsa_circ_308726,RMVar_hsa_circ_55381,RMVar_hsa_circ_67355,RMVar_hsa_circ_160023,RMVar_hsa_circ_326304,RMVar_hsa_circ_44534,RMVar_hsa_circ_160025,RMVar_hsa_circ_376007,RMVar_hsa_circ_70361,RMVar_hsa_circ_160026,RMVar_hsa_circ_304780,RMVar_hsa_circ_313083,RMVar_hsa_circ_304077,RMVar_hsa_circ_160029,RMVar_hsa_circ_88262,RMVar_hsa_circ_160027,RMVar_hsa_circ_160028,RMVar_hsa_circ_116976,RMVar_hsa_circ_340070,RMVar_hsa_circ_160030 85703 RMVar_ID_85703 Human_SNP_ID_515969690 m1A Human chr12 - 111766986 111766986 111766986 CAGGCGGGGCCCGAAGCGGGCGGCAGCGCGCAACATCGCAGCGGGCTAGCGGACAGCGAGCGGAC CAGGCGGGGCCCGAAGCGGGCGGCAGCGCGCAGCATCGCAGCGGGCTAGCGGACAGCGAGCGGAC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:111766941..111767094 26863196 MeRIP-seq:(Medium) rs777511085 Functional Loss SNV dbSNP153 33..33 33 - - - 85704 RMVar_ID_85704 Human_SNP_ID_515969709 m1A Human chr12 - 111767017 111767017 111767017 GGGTGGCGGCGGCTGACAAGAGGCGGCGGCCCAGGCGGGGCCCGAAGCGGGCGGCAGCGCGCAAC GGGTGGCGGCGGCTGACAAGAGGCGGCGGCCCGGGCGGGGCCCGAAGCGGGCGGCAGCGCGCAAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr12:111766937..111767100;chr12:111766966..111767135 26863196 MeRIP-seq:(Medium) rs1215850690 Functional Loss SNV dbSNP153 33..33 33 - - - 85705 RMVar_ID_85705 Human_SNP_ID_515969715 m1A Human chr12 - 111767029 111767029 111767029 CAGGCACGGCCTGGGTGGCGGCGGCTGACAAGAGGCGGCGGCCCAGGCGGGGCCCGAAGCGGGCG CAGGCACGGCCTGGGTGGCGGCGGCTGACAAGCGGCGGCGGCCCAGGCGGGGCCCGAAGCGGGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:111766979..111767134 26863196 MeRIP-seq:(Medium) rs916384497 Functional Loss SNV dbSNP153 33..33 33 - - - 85706 RMVar_ID_85706 Human_SNP_ID_515969723 m1A Human chr12 + 111767050 111767050 111767050 GGGCCGCCGCCTCTTGTCAGCCGCCGCCACCCAGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGG GGGCCGCCGCCTCTTGTCAGCCGCCGCCACCCGGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGG A G AC002996.1,ALDH2 Ensembl:ENSG00000257767,Ensembl:ENSG00000111275 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:111766926..111767125 26863410 MeRIP-seq:(Medium) rs1330573776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_410825,Human_RBP_ID_4246999,Human_RBP_ID_8787366,Human_RBP_ID_9279212,Human_RBP_ID_17357375,Human_RBP_ID_22436110,Human_RBP_ID_26807070 Human_Splice_Rec_1425761,Human_Splice_Rec_1425783,Human_Splice_Rec_1425807 Human_miRNA_ID_2491534 RMVar_hsa_circ_121972,RMVar_hsa_circ_160040 85707 RMVar_ID_85707 Human_SNP_ID_515969739 m1A Human chr12 + 111767074 111767074 111767074 CGCCACCCAGGCCGTGCCTGCCCCCAACCAGCAGCCCGAGGTCTTCTGCAACCAGGTGAGCCCAC CGCCACCCAGGCCGTGCCTGCCCCCAACCAGCGGCCCGAGGTCTTCTGCAACCAGGTGAGCCCAC A G AC002996.1,ALDH2 Ensembl:ENSG00000257767,Ensembl:ENSG00000111275 Protein coding,Protein coding intron,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:111766970..111767100 26863196 MeRIP-seq:(Medium) rs1275543545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246999,Human_RBP_ID_9279212,Human_RBP_ID_17357375,Human_RBP_ID_22436110 Human_Splice_Rec_1425761,Human_Splice_Rec_1425783,Human_Splice_Rec_1425807 Human_miRNA_ID_2579797 RMVar_hsa_circ_121972,RMVar_hsa_circ_160040 85708 RMVar_ID_85708 Human_SNP_ID_515987059 m1A Human chr12 + 111841113 111841113 111841113 TCACCCTTTATCAGTCTCCTCCTACTCGATCTACTCCAGCTACAATGACCTTCTTGCTGATTCTT TCACCCTTTATCAGTCTCCTCCTACTCGATCTTCTCCAGCTACAATGACCTTCTTGCTGATTCTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:111841076..111841306 26863196 MeRIP-seq:(Medium) rs1224080956 Functional Loss SNV dbSNP153 33..33 33 - - - 85709 RMVar_ID_85709 Human_SNP_ID_515987328 m1A Human chr12 - 111842123 111842123 111842123 CCTGCCGCCCAGCTTCGTGACTCCACGGCCCCACGCGCCCCTTGCTGCCTTCCGCTGGGGTTTCC CCTGCCGCCCAGCTTCGTGACTCCACGGCCCCCCGCGCCCCTTGCTGCCTTCCGCTGGGGTTTCC T G MAPKAPK5-AS1 Ensembl:ENSG00000234608 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:111842026..111842746;chr12:111842026..111842726 26863196 MeRIP-seq:(Medium) rs1299114828 Functional Loss SNV dbSNP153 33..33 33 - - - 85710 RMVar_ID_85710 Human_SNP_ID_515987340 m1A Human chr12 - 111842166 111842166 111842166 CTCACGCACGCGCTGTGCCCCGCGGGAGCTCCAGGCCGCCCCTCCTGCCGCCCAGCTTCGTGACT CTCACGCACGCGCTGTGCCCCGCGGGAGCTCCTGGCCGCCCCTCCTGCCGCCCAGCTTCGTGACT T A MAPKAPK5-AS1 Ensembl:ENSG00000234608 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:111842111..111842251 26863196 MeRIP-seq:(Medium) rs891147331 Functional Loss SNV dbSNP153 33..33 33 - - - 85711 RMVar_ID_85711 Human_SNP_ID_516027991 m1A Human chr12 + 112013492 112013492 112013492 GGCGATATGGCTGCCGCTGTGCCCCGCGCCGCATTTCTCTCCCCGCTGCTTCCCCTTCTCCTGGG GGCGATATGGCTGCCGCTGTGCCCCGCGCCGCTTTTCTCTCCCCGCTGCTTCCCCTTCTCCTGGG A T ERP29 Ensembl:ENSG00000089248 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:112013426..112013625;chr12:112013396..112014595;chr12:112013414..112014595 26863196 MeRIP-seq:(Medium) rs762048210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229751,Human_RBP_ID_410946,Human_RBP_ID_4201331,Human_RBP_ID_5416662,Human_RBP_ID_5437262,Human_RBP_ID_5490892,Human_RBP_ID_17357376,Human_RBP_ID_18188887,Human_RBP_ID_22436113,Human_RBP_ID_27418507 85712 RMVar_ID_85712 Human_SNP_ID_516029501 m1A Human chr12 - 112019807 112019807 112019807 AAGACGCTTGAACTCATCCTGCTTCTCACCGTAGGGGTACTGGGTGTCGAACTTCACCAAGACGA AAGACGCTTGAACTCATCCTGCTTCTCACCGTGGGGGTACTGGGTGTCGAACTTCACCAAGACGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:112019696..112019878 26863196 MeRIP-seq:(Medium) rs757471812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18617967 85713 RMVar_ID_85713 Human_SNP_ID_516030248 m1A Human chr12 + 112022554 112022551 112022554 CAGAGATGACACGGATCGCCAGGCTGATTGAGAAGAACAAGATGAGTGACGGGAAGAAGGAGGAG CAGAGATGACACGGATCGCCAGGCTGATTG___AGAACAAGATGAGTGACGGGAAGAAGGAGGAG GAGA G ERP29 Ensembl:ENSG00000089248 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112022151..112023000 26863196 MeRIP-seq:(Medium) rs1354738782 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_410964,Human_RBP_ID_809953,Human_RBP_ID_1464698,Human_RBP_ID_1787182,Human_RBP_ID_2305093,Human_RBP_ID_3393502,Human_RBP_ID_6133798,Human_RBP_ID_9011250,Human_RBP_ID_11817377,Human_RBP_ID_18433542,Human_RBP_ID_18617976,Human_RBP_ID_23538541,Human_RBP_ID_26321018,Human_RBP_ID_26421629 Human_miRNA_ID_1527852 85714 RMVar_ID_85714 Human_SNP_ID_516030258 m1A Human chr12 + 112022575 112022573 112022576 GGCTGATTGAGAAGAACAAGATGAGTGACGGGAAGAAGGAGGAGCTCCAGAAGAGCTTAAACATC GGCTGATTGAGAAGAACAAGATGAGTGACGG___GAAGGAGGAGCTCCAGAAGAGCTTAAACATC GGAA G ERP29 Ensembl:ENSG00000089248 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:112022158..112022975 26863196 MeRIP-seq:(Medium) rs1352097022 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_410964,Human_RBP_ID_1464700,Human_RBP_ID_3393502,Human_RBP_ID_4201361,Human_RBP_ID_6133798,Human_RBP_ID_11817377,Human_RBP_ID_22757366,Human_RBP_ID_23538541,Human_RBP_ID_26321018,Human_RBP_ID_26421629 85715 RMVar_ID_85715 Human_SNP_ID_516049088 m1A Human chr12 + 112101032 112101032 112101032 CACTTCCTCACTCATTTCTTCATTCCAACTGCACAAGCCTTTGCTTACATCCTCAAGTGGACCAA CACTTCCTCACTCATTTCTTCATTCCAACTGCGCAAGCCTTTGCTTACATCCTCAAGTGGACCAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:112100982..112101179 26863196 MeRIP-seq:(Medium) rs998352202 Functional Loss SNV dbSNP153 33..33 33 - - - 85716 RMVar_ID_85716 Human_SNP_ID_516049736 m1A Human chr12 - 112103887 112103887 112103887 CTGTCAGATCAGCTCTTAGGAGTAGGAACACAAACCCTGTTGTGAACTATGCATGTGAGGAATCG CTGTCAGATCAGCTCTTAGGAGTAGGAACACACACCCTGTTGTGAACTATGCATGTGAGGAATCG T G NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:112103878..112104007 32194978 MeRIP-seq:(Medium) rs987346708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1787380,Human_RBP_ID_11820102 85717 RMVar_ID_85717 Human_SNP_ID_516054977 m1A Human chr12 - 112125613 112125613 112125613 CAGCCGCGTGCCGCCGCTACACCTCACCAGGGACGAGAGGAGAAACGCTGAGTTGACACACTAGC CAGCCGCGTGCCGCCGCTACACCTCACCAGGGGCGAGAGGAGAAACGCTGAGTTGACACACTAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:112125576..112125662 26863196 MeRIP-seq:(Medium) rs1425059472 Functional Loss SNV dbSNP153 33..33 33 - - - 85718 RMVar_ID_85718 Human_SNP_ID_516054978 m1A Human chr12 - 112125620 112125620 112125620 GGATCTCCAGCCGCGTGCCGCCGCTACACCTCACCAGGGACGAGAGGAGAAACGCTGAGTTGACA GGATCTCCAGCCGCGTGCCGCCGCTACACCTCCCCAGGGACGAGAGGAGAAACGCTGAGTTGACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr12:112125590..112125700;chr12:112125569..112125781;chr12:112125580..112125796 26863196 MeRIP-seq:(Medium) rs931609082 Functional Loss SNV dbSNP153 33..33 33 - - - 85719 RMVar_ID_85719 Human_SNP_ID_516054981 m1A Human chr12 - 112125627 112125626 112125627 CCACAGGGGATCTCCAGCCGCGTGCCGCCGCTACACCTCACCAGGGACGAGAGGAGAAACGCTGA CCACAGGGGATCTCCAGCCGCGTGCCGCCGCT_CACCTCACCAGGGACGAGAGGAGAAACGCTGA GT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:112125578..112125742 26863196 MeRIP-seq:(Medium) rs1217143285 Functional Loss DEL dbSNP153 33..33 33 - - - 85720 RMVar_ID_85720 Human_SNP_ID_516061042 m1A Human chr12 + 112151951 112151951 112151951 GAGATCAACATCAGGCCCCAGACCTGGGTGCCAGCCCAGCTCTCCTTGTGTGCCGAAGCTCAGCA GAGATCAACATCAGGCCCCAGACCTGGGTGCCGGCCCAGCTCTCCTTGTGTGCCGAAGCTCAGCA A G TRAFD1 Ensembl:ENSG00000135148 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:112151901..112152050 32194978 MeRIP-seq:(Medium) rs1273209887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8787371 Human_miRNA_ID_2554247,Human_miRNA_ID_2621291 RMVar_hsa_circ_26662,RMVar_hsa_circ_75980,RMVar_hsa_circ_86434,RMVar_hsa_circ_160125,RMVar_hsa_circ_92130,RMVar_hsa_circ_160127,RMVar_hsa_circ_160128,RMVar_hsa_circ_76049,RMVar_hsa_circ_61043,RMVar_hsa_circ_160130,RMVar_hsa_circ_376853 85721 RMVar_ID_85721 Human_SNP_ID_516061353 m1A Human chr12 + 112153203 112153203 112153203 TGTTGGGGCCTAAATTTGGGGGCTTTTGGGCAACCTCTCCGTGTACTGCGTCTGTCCACACTCGA TGTTGGGGCCTAAATTTGGGGGCTTTTGGGCAGCCTCTCCGTGTACTGCGTCTGTCCACACTCGA A G TRAFD1 Ensembl:ENSG00000135148 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:112152960..112153210 32194978 MeRIP-seq:(Medium) rs1307884219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5139710,Human_RBP_ID_8178153,Human_RBP_ID_17831120,Human_RBP_ID_24464102,Human_RBP_ID_26412043 RMVar_hsa_circ_86434,RMVar_hsa_circ_160125,RMVar_hsa_circ_160128,RMVar_hsa_circ_76049,RMVar_hsa_circ_96804,RMVar_hsa_circ_160132 85722 RMVar_ID_85722 Human_SNP_ID_516063639 m1A Human chr12 - 112163143 112163143 112163143 GCTGTGCAAGTTCATCAAGTTTGCCTGCAACCAGGAGCGCATCCCGTTCACCTGCCCCTGCAAAG GCTGTGCAAGTTCATCAAGTTTGCCTGCAACCTGGAGCGCATCCCGTTCACCTGCCCCTGCAAAG T A HECTD4 Ensembl:ENSG00000173064 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112163093..112163194 26863196 MeRIP-seq:(Medium) rs752271888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_265564 85723 RMVar_ID_85723 Human_SNP_ID_516092443 m1A Human chr12 - 112285764 112285764 112285764 ATGTCGGTGGGGAGGGTGAGGGGCAGTTAGAAAAGTGGAACTAGATCGTAGTAGCAAGGATGGGT ATGTCGGTGGGGAGGGTGAGGGGCAGTTAGAAGAGTGGAACTAGATCGTAGTAGCAAGGATGGGT T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112285713..112285802 26863196 MeRIP-seq:(Medium) rs533246617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96738,RMVar_hsa_circ_160136,RMVar_hsa_circ_92094,RMVar_hsa_circ_160156,RMVar_hsa_circ_92637,RMVar_hsa_circ_160206,RMVar_hsa_circ_114486,RMVar_hsa_circ_160208,RMVar_hsa_circ_160215,RMVar_hsa_circ_110740,RMVar_hsa_circ_266808,RMVar_hsa_circ_125121,RMVar_hsa_circ_160224,RMVar_hsa_circ_98406,RMVar_hsa_circ_160225,RMVar_hsa_circ_26948,RMVar_hsa_circ_59030,RMVar_hsa_circ_37936,RMVar_hsa_circ_29465,RMVar_hsa_circ_311075,RMVar_hsa_circ_24813 85724 RMVar_ID_85724 Human_SNP_ID_516095260 m1A Human chr12 - 112297169 112297169 112297169 GCACCTACATTCACTGCACCTACACCCTCTGCACCTACACCTTCTGCATCTACATCCACTGTACC GCACCTACATTCACTGCACCTACACCCTCTGCGCCTACACCTTCTGCATCTACATCCACTGTACC T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112297118..112297187 26863196 MeRIP-seq:(Medium) rs1202555373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194463,Human_RBP_ID_260100,Human_RBP_ID_2365604,Human_RBP_ID_9415939,Human_RBP_ID_24529957,Human_RBP_ID_26755630,Human_RBP_ID_26806082 RMVar_hsa_circ_96738,RMVar_hsa_circ_160136,RMVar_hsa_circ_92094,RMVar_hsa_circ_160156,RMVar_hsa_circ_92637,RMVar_hsa_circ_160206,RMVar_hsa_circ_114486,RMVar_hsa_circ_160208,RMVar_hsa_circ_160215,RMVar_hsa_circ_110740,RMVar_hsa_circ_266808,RMVar_hsa_circ_125121,RMVar_hsa_circ_160224,RMVar_hsa_circ_98406,RMVar_hsa_circ_160225,RMVar_hsa_circ_26948,RMVar_hsa_circ_59030,RMVar_hsa_circ_37936,RMVar_hsa_circ_29465,RMVar_hsa_circ_311075,RMVar_hsa_circ_24813 85725 RMVar_ID_85725 Human_SNP_ID_516114365 m1A Human chr12 + 112382302 112382302 112382302 CGCCCTAGGCGGTCCGAGTCGCCATACCCCCGACCCCGGCCCGGGAGACCCCGGCCCTGCCGCCG CGCCCTAGGCGGTCCGAGTCGCCATACCCCCGCCCCCGGCCCGGGAGACCCCGGCCCTGCCGCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:112381986..112382409 26863196 MeRIP-seq:(Medium) rs903541536 Functional Loss SNV dbSNP153 33..33 33 - - - 85726 RMVar_ID_85726 Human_SNP_ID_516114375 m1A Human chr12 - 112382327 112382325 112382328 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGGGCCGGGGTCTCCCGGGCCGGGGTCGGGGGT GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG___GGCCGGGGTCTCCCGGGCCGGGGTCGGGGGT CCTG C HECTD4 Ensembl:ENSG00000173064 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr12:112381951..112382400;chr12:112382210..112382355;chr12:112382250..112382360 26863196,26863410 MeRIP-seq:(Medium) rs1433130590 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4250094,Human_RBP_ID_5314668,Human_RBP_ID_5521761,Human_RBP_ID_9279236,Human_RBP_ID_9322707,Human_RBP_ID_11823553,Human_RBP_ID_18977839,Human_RBP_ID_22793048 85727 RMVar_ID_85727 Human_SNP_ID_516114378 m1A Human chr12 - 112382327 112382327 112382327 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGGGCCGGGGTCTCCCGGGCCGGGGTCGGGGGT GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGCCGGGGTCTCCCGGGCCGGGGTCGGGGGT T C HECTD4 Ensembl:ENSG00000173064 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Starvation treatment chr12:112381951..112382400;chr12:112382210..112382355;chr12:112382250..112382360 26863196,26863410 MeRIP-seq:(Medium) rs1364768447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4250094,Human_RBP_ID_5314668,Human_RBP_ID_5521761,Human_RBP_ID_9279236,Human_RBP_ID_9322707,Human_RBP_ID_11823553,Human_RBP_ID_18977839,Human_RBP_ID_22793048 85728 RMVar_ID_85728 Human_SNP_ID_516114413 m1A Human chr12 + 112382364 112382360 112382364 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCCTCAGGAGCAGGATCCGCCTCTGCCGCTCGGCAACC CCGCCGCCGCCGCCGCCGCCGCCGCCGCC____GGAGCAGGATCCGCCTCTGCCGCTCGGCAACC CCTCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112381946..112382407 26863196 MeRIP-seq:(Medium) rs1355824442 Functional Loss DEL dbSNP153 30..33 33 - - - 85729 RMVar_ID_85729 Human_SNP_ID_516114415 m1A Human chr12 + 112382373 112382365 112382374 CCGCCGCCGCCGCCGCCGCCCTCAGGAGCAGGATCCGCCTCTGCCGCTCGGCAACCAACTGTCAG CCGCCGCCGCCGCCGCCGCCCTCAG_________CCGCCTCTGCCGCTCGGCAACCAACTGTCAG GGAGCAGGAT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:112382221..112382456 26863196 MeRIP-seq:(Medium) rs1291009074 Functional Loss DEL dbSNP153 26..34 33 - - - 85730 RMVar_ID_85730 Human_SNP_ID_516120721 m1A Human chr12 + 112405976 112405976 112405976 ATTTTTACATTGCTGATATCGATTTTGGTTGAAGTGGCAATGACAAATTTCTGGTGTGTTCTTCG ATTTTTACATTGCTGATATCGATTTTGGTTGAGGTGGCAATGACAAATTTCTGGTGTGTTCTTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:112405933..112406012 26863196 MeRIP-seq:(Medium) rs17851812 Functional Loss SNV dbSNP153 33..33 33 - - - 85731 RMVar_ID_85731 Human_SNP_ID_516124255 m1A Human chr12 + 112418971 112418971 112418971 AGCTGCACAGTCTCCGGGATCCCCAGGCCTGGAGGGGGGTCTGTGCGCGGCCGGCTGGCTCTGCC AGCTGCACAGTCTCCGGGATCCCCAGGCCTGGTGGGGGGTCTGTGCGCGGCCGGCTGGCTCTGCC A T PTPN11 Ensembl:ENSG00000179295 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:112418926..112419125 26863196 MeRIP-seq:(Medium) rs1231875732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230172,Human_RBP_ID_411111,Human_RBP_ID_754701,Human_RBP_ID_4202008,Human_RBP_ID_5462458,Human_RBP_ID_5490909,Human_RBP_ID_8786922,Human_RBP_ID_9255592,Human_RBP_ID_9279237,Human_RBP_ID_9322709,Human_RBP_ID_18457298,Human_RBP_ID_26768419 85732 RMVar_ID_85732 Human_SNP_ID_516124287 m1A Human chr12 - 112419031 112419031 112419031 TCCGCTGGGCTCGGTCACATCGGGCTGGCCCGAGGGAGGCCCGCTCGGGACCGGACGCGGGGCAG TCCGCTGGGCTCGGTCACATCGGGCTGGCCCGGGGGAGGCCCGCTCGGGACCGGACGCGGGGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:112418985..112419081 32194978 MeRIP-seq:(Medium) rs1375203449 Functional Loss SNV dbSNP153 33..33 33 - - - 85733 RMVar_ID_85733 Human_SNP_ID_516139172 m1A Human chr12 - 112483762 112483762 112483762 TTCACTGAATCCCTGCATGTCTGCCTCCAGTCAGCTCTACTGGGTCCTCTTCTTTCAGGCACCCT TTCACTGAATCCCTGCATGTCTGCCTCCAGTCCGCTCTACTGGGTCCTCTTCTTTCAGGCACCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:112483759..112483891 26863196 MeRIP-seq:(Medium) rs537096208 Functional Loss SNV dbSNP153 33..33 33 - - - 85734 RMVar_ID_85734 Human_SNP_ID_516144434 m1A Human chr12 - 112508424 112508424 112508424 GAAACCACCTCTTTGGAACTTTCCTTTCCACAACTTTTTTTTTAAAACTTCACCTCGAGCTTTCT GAAACCACCTCTTTGGAACTTTCCTTTCCACAGCTTTTTTTTTAAAACTTCACCTCGAGCTTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:112508376..112508537 26863196 MeRIP-seq:(Medium) rs1199056710 Functional Loss SNV dbSNP153 33..33 33 - - - 85735 RMVar_ID_85735 Human_SNP_ID_516300115 m1A Human chr12 - 113158903 113158900 113158903 AGGGCGCCTTCGGCCGGGGTGCCCGCTCCAAGAAGGGCAAGATGCGGAAGAGGATGTGAGGACCA AGGGCGCCTTCGGCCGGGGTGCCCGCTCCAAG___GGCAAGATGCGGAAGAGGATGTGAGGACCA CCTT C DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:113158670..113159143 26863196 MeRIP-seq:(Medium) rs775014742 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_27557609 85736 RMVar_ID_85736 Human_SNP_ID_516300772 m1A Human chr12 + 113161292 113161292 113161292 TGGCTCTCACCTTGGCCACGGTCTCGCTTCCCACCTCTTCGCTCTGGGCCTCGCCGGTCAGATGC TGGCTCTCACCTTGGCCACGGTCTCGCTTCCCCCCTCTTCGCTCTGGGCCTCGCCGGTCAGATGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:113159076..113161416 26863196 MeRIP-seq:(Medium) rs1044817493 Functional Loss SNV dbSNP153 33..33 33 - - - 85737 RMVar_ID_85737 Human_SNP_ID_516300796 m1A Human chr12 + 113161339 113161339 113161339 GCCTCGCCGGTCAGATGCCCCTTCTTCGTCCGAGTCACGATCATCAATTTTCTGTTTCTGTTTCC GCCTCGCCGGTCAGATGCCCCTTCTTCGTCCGTGTCACGATCATCAATTTTCTGTTTCTGTTTCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:113161218..113161432 26863196 MeRIP-seq:(Medium) rs1435371355 Functional Loss SNV dbSNP153 33..33 33 - - - 85738 RMVar_ID_85738 Human_SNP_ID_516301060 m1A Human chr12 + 113161974 113161974 113161974 TCTTCTTCTTGTCTTCCTGTCCTGACTGTCCCACAAACCGCTTCTTCTTACGGTCCCTGCAGGAG TCTTCTTCTTGTCTTCCTGTCCTGACTGTCCCGCAAACCGCTTCTTCTTACGGTCCCTGCAGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:113161838..113162041;chr12:113161842..113162062;chr12:113161826..113162063;chr12:113161851..113169885 26863196 MeRIP-seq:(Medium) rs1177530419 Functional Loss SNV dbSNP153 33..33 33 - - - 85739 RMVar_ID_85739 Human_SNP_ID_516301688 m1A Human chr12 + 113164029 113164029 113164029 ATGGGCTGCTGGGACTTAGCCACCCCTTCCCCATACCCCAGGTCCAGGGTCCCCAGGGTGGAACC ATGGGCTGCTGGGACTTAGCCACCCCTTCCCCCTACCCCAGGTCCAGGGTCCCCAGGGTGGAACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113164025..113164324 26863196 MeRIP-seq:(Medium) rs750475044 Functional Loss SNV dbSNP153 33..33 33 - - - 85740 RMVar_ID_85740 Human_SNP_ID_516303244 m1A Human chr12 + 113169820 113169820 113169820 GTCGGGCGAGGGTGAGGGAGCGGCCCAGGAACAGGTGCAGATCCAGCAGGTAGGGGATTTCATCA GTCGGGCGAGGGTGAGGGAGCGGCCCAGGAACTGGTGCAGATCCAGCAGGTAGGGGATTTCATCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:113169721..113169925 26863196 MeRIP-seq:(Medium) rs1341941005 Functional Loss SNV dbSNP153 33..33 33 - - - 85741 RMVar_ID_85741 Human_SNP_ID_516304509 m1A Human chr12 - 113174645 113174645 113174645 TTGTGGCCACGAAGCACCACGCCGAGTACCTCACTGAGGTGAGCAGGGTCCTGAGTGGGAGGAGC TTGTGGCCACGAAGCACCACGCCGAGTACCTCGCTGAGGTGAGCAGGGTCCTGAGTGGGAGGAGC T C DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113162934..113177142 32194978 MeRIP-seq:(Medium) rs140924337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059230 Human_Splice_Rec_1428177,Human_Splice_Rec_1428215 Human_miRNA_ID_2007240 RMVar_hsa_circ_105766,RMVar_hsa_circ_373685,RMVar_hsa_circ_19945,RMVar_hsa_circ_111144,RMVar_hsa_circ_160306,RMVar_hsa_circ_160307,RMVar_hsa_circ_160308,RMVar_hsa_circ_355907,RMVar_hsa_circ_160311,RMVar_hsa_circ_120832,RMVar_hsa_circ_334607,RMVar_hsa_circ_13670,RMVar_hsa_circ_124474,RMVar_hsa_circ_160313,RMVar_hsa_circ_104211,RMVar_hsa_circ_160314,RMVar_hsa_circ_160312 85742 RMVar_ID_85742 Human_SNP_ID_516305717 m1A Human chr12 + 113179043 113179043 113179043 CAGTGAACTTGCCTAGCTGAGAAGAGAAAGTGATTGAGAGAGGGCAGGGGTGAGATGACAGCACA CAGTGAACTTGCCTAGCTGAGAAGAGAAAGTGGTTGAGAGAGGGCAGGGGTGAGATGACAGCACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113179041..113179134 26863196 MeRIP-seq:(Medium) rs1453229035 Functional Loss SNV dbSNP153 33..33 33 - - - 85743 RMVar_ID_85743 Human_SNP_ID_516305807 m1A Human chr12 - 113179225 113179225 113179225 CCTCCTCCCAATGTTCGAGCGGCTCAAGACCCACAGTGCCCAGACCGGGGCCCGCGCCCTCATCC CCTCCTCCCAATGTTCGAGCGGCTCAAGACCCCCAGTGCCCAGACCGGGGCCCGCGCCCTCATCC T G DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113179176..113179280 26863196 MeRIP-seq:(Medium) rs767660701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22793078,Human_RBP_ID_26901437 Human_Splice_Rec_1428165,Human_Splice_Rec_1428203,Human_Splice_Rec_1428265,Human_Splice_Rec_1428281 Human_miRNA_ID_2157699 RMVar_hsa_circ_2127,RMVar_hsa_circ_355907,RMVar_hsa_circ_160311,RMVar_hsa_circ_334607,RMVar_hsa_circ_13670,RMVar_hsa_circ_104211,RMVar_hsa_circ_160314,RMVar_hsa_circ_307837,RMVar_hsa_circ_295429,RMVar_hsa_circ_71574,RMVar_hsa_circ_160315,RMVar_hsa_circ_160316,RMVar_hsa_circ_160317,RMVar_hsa_circ_100572,RMVar_hsa_circ_272039,RMVar_hsa_circ_327108,RMVar_hsa_circ_160318 85744 RMVar_ID_85744 Human_SNP_ID_516307436 m1A Human chr12 - 113185225 113185225 113185225 CGCATGTTCGGGCCCGAGACCCGGCTCCGGGCAGCGCCTCGAGGCCTCAGTTTCCCCAGCTGGGG CGCATGTTCGGGCCCGAGACCCGGCTCCGGGCCGCGCCTCGAGGCCTCAGTTTCCCCAGCTGGGG T G DDX54 Ensembl:ENSG00000123064 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:113185223..113185383 26863196 MeRIP-seq:(Medium) rs1459927591 Functional Loss SNV dbSNP153 33..33 33 - - - 85745 RMVar_ID_85745 Human_SNP_ID_516307502 m1A Human chr12 - 113185337 113185337 113185337 AGCGCCGAGGCGCGGCCTCCCAGGCCCGCGGCAGCGACTCGGAGGACGGCGAGTTTGAGATCCAG AGCGCCGAGGCGCGGCCTCCCAGGCCCGCGGCGGCGACTCGGAGGACGGCGAGTTTGAGATCCAG T C DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:113180942..113185475 26863196 MeRIP-seq:(Medium) rs1409049845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4202405,Human_RBP_ID_17650234,Human_RBP_ID_26322053 Human_Splice_Rec_1428159,Human_Splice_Rec_1428197,Human_Splice_Rec_1428259 85746 RMVar_ID_85746 Human_SNP_ID_516307556 m1A Human chr12 - 113185410 113185408 113185410 GACAAGGGCCCGGCGGCTGGACCTCGGTCGCGAGCTGCCATGGCCCAGTGGAGGAAGAAGAAAGG GACAAGGGCCCGGCGGCTGGACCTCGGTCGCG__CTGCCATGGCCCAGTGGAGGAAGAAGAAAGG GCT G DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:113185276..113185450 26863196 MeRIP-seq:(Medium) rs753660481 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_411272,Human_RBP_ID_4247012,Human_RBP_ID_5416673,Human_RBP_ID_8786938,Human_RBP_ID_9322714,Human_RBP_ID_22573469 85747 RMVar_ID_85747 Human_SNP_ID_516307786 m1A Human chr12 - 113185776 113185776 113185776 GCACAGGCTACGTGTGAACGGCCCGCGAATCCAGAAACCCAGAACCCAGCACTTTGCACCCAGCA GCACAGGCTACGTGTGAACGGCCCGCGAATCCGGAAACCCAGAACCCAGCACTTTGCACCCAGCA T C AC089999.3 Ensembl:ENSG00000257286 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113185618..113185838 26863196 MeRIP-seq:(Medium) rs532443329 Functional Loss SNV dbSNP153 33..33 33 - - - 85748 RMVar_ID_85748 Human_SNP_ID_516308070 m1A Human chr12 + 113186786 113186786 113186786 CCCCCGTGGAGCTGGCCGTCAGTGGGATGCAGACCCTCGGCCTTCAGCACCGCTGCCGAGGTGGC CCCCCGTGGAGCTGGCCGTCAGTGGGATGCAGGCCCTCGGCCTTCAGCACCGCTGCCGAGGTGGC A G RITA1 Ensembl:ENSG00000139405 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113186735..113186935 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 85749 RMVar_ID_85749 Human_SNP_ID_516309350 m1A Human chr12 + 113191505 113191505 113191505 CCCAGGGAGGCACCACTGCGAGCCATTCACCCAGCTGGTCCCTCCAAGACAGAGCCGGGGCCAGC CCCAGGGAGGCACCACTGCGAGCCATTCACCCCGCTGGTCCCTCCAAGACAGAGCCGGGGCCAGC A C RITA1 Ensembl:ENSG00000139405 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:113191456..113191600 26863196 MeRIP-seq:(Medium) rs1401029956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17809953 85750 RMVar_ID_85750 Human_SNP_ID_516309507 m1A Human chr12 - 113191877 113191877 113191877 CCTGGGGTTCCCTGGGTGATGAATGTCCTCCTACCCTGGCAAGGGGCCATACCTGTCGCCGTGGC CCTGGGGTTCCCTGGGTGATGAATGTCCTCCTTCCCTGGCAAGGGGCCATACCTGTCGCCGTGGC T A AC089999.3 Ensembl:ENSG00000257286 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113191827..113191975 32194978 MeRIP-seq:(Medium) rs1290403251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160320 85751 RMVar_ID_85751 Human_SNP_ID_516310499 m1A Human chr12 - 113195780 113195780 113195780 GCTGGTGGGAGAGTTTGCGCAGATCCGGGAAGAGCGGGAGATCAACTCCAAGAAAAGGATGGAGG GCTGGTGGGAGAGTTTGCGCAGATCCGGGAAGCGCGGGAGATCAACTCCAAGAAAAGGATGGAGG T G IQCD Ensembl:ENSG00000166578 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113195624..113195852 26863196 MeRIP-seq:(Medium) rs1233424159 Functional Loss SNV dbSNP153 33..33 33 - - - 85752 RMVar_ID_85752 Human_SNP_ID_516316692 m1A Human chr12 + 113221534 113221534 113221534 GCGGCGGCTTCGGCGGCTGCGGCGGCTGCAACAGCTTCGGGCTCGGGGTTTTGGCGGCGGCGCCG GCGGCGGCTTCGGCGGCTGCGGCGGCTGCAACGGCTTCGGGCTCGGGGTTTTGGCGGCGGCGCCG A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113221484..113221685 26863196 MeRIP-seq:(Medium) rs1204717660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4202477,Human_RBP_ID_9322715,Human_RBP_ID_18417675,Human_RBP_ID_22436700,Human_RBP_ID_23125117 Human_Splice_Rec_1428349,Human_Splice_Rec_1428355,Human_Splice_Rec_1428361,Human_Splice_Rec_1428415,Human_Splice_Rec_1428421,Human_Splice_Rec_1428477,Human_Splice_Rec_1428483 85753 RMVar_ID_85753 Human_SNP_ID_516316720 m1A Human chr12 - 113221614 113221614 113221614 CGCATCCCTCGGATTCTTACACGCGCCGCCCCAGCAACCCGGACCGCGCGCCGGGGTCCGCACCG CGCATCCCTCGGATTCTTACACGCGCCGCCCCGGCAACCCGGACCGCGCGCCGGGGTCCGCACCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:113221517..113221630 26863410 MeRIP-seq:(Medium) rs980537022 Functional Loss SNV dbSNP153 33..33 33 - - - 85754 RMVar_ID_85754 Human_SNP_ID_516322063 m1A Human chr12 + 113244836 113244836 113244836 TGGATGAAGAAACTGAGGCTCTGGGGATTAAGATCGTGAACTGTGGGGAGTGGAGGAGGCACAGC TGGATGAAGAAACTGAGGCTCTGGGGATTAAGGTCGTGAACTGTGGGGAGTGGAGGAGGCACAGC A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:113244830..113244946 26863196 MeRIP-seq:(Medium) rs1459313774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17112383 RMVar_hsa_circ_47588,RMVar_hsa_circ_272643,RMVar_hsa_circ_160321 85755 RMVar_ID_85755 Human_SNP_ID_516323110 m1A Human chr12 - 113248545 113248541 113248545 TGGCTGCTTTGTCACACCTTCCAGTTTCCACAAACATTTTATCAGAGGCTACCCTTGGCCTCCCC TGGCTGCTTTGTCACACCTTCCAGTTTCCACA____TTTTATCAGAGGCTACCCTTGGCCTCCCC ATGTT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113248540..113248742 26863196 MeRIP-seq:(Medium) rs952467685 Functional Loss DEL dbSNP153 33..36 33 - - - 85756 RMVar_ID_85756 Human_SNP_ID_516329756 m1A Human chr12 + 113276971 113276971 113276971 CACCTTCAATGACATTGAGAAACGCAAGTTCAAGTCTTTGCTACTGCACAAGCGAACCGCTATCC CACCTTCAATGACATTGAGAAACGCAAGTTCAGGTCTTTGCTACTGCACAAGCGAACCGCTATCC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs760507745 Functional Loss SNV dbSNP153 33..33 33 - - - 85757 RMVar_ID_85757 Human_SNP_ID_516330276 m1A Human chr12 - 113278909 113278909 113278909 ACACACACACACCCCTCTGAACCTCTCCTCAGACGCTTATCTGTGGTCTCTGAAAACCTCCATCG ACACACACACACCCCTCTGAACCTCTCCTCAGTCGCTTATCTGTGGTCTCTGAAAACCTCCATCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113278858..113279024 26863196 MeRIP-seq:(Medium) rs1435923865 Functional Loss SNV dbSNP153 33..33 33 - - - 85758 RMVar_ID_85758 Human_SNP_ID_516334926 m1A Human chr12 + 113296047 113296047 113296047 GTGCAGCCCCCGCCGCCCAGCAGCCCCCAGGCAGCCGCCAGCGCTCCCAGACCGTTACCTAGCCC GTGCAGCCCCCGCCGCCCAGCAGCCCCCAGGCCGCCGCCAGCGCTCCCAGACCGTTACCTAGCCC A C TPCN1 Ensembl:ENSG00000186815 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113295960..113296047 26863196 MeRIP-seq:(Medium) rs752033068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19701763,Human_RBP_ID_26322063 Human_Splice_Rec_1428414,Human_Splice_Rec_1428476,Human_Splice_Rec_1428534,Human_Splice_Rec_1428588,Human_Splice_Rec_1428640,Human_Splice_Rec_1428734,Human_Splice_Rec_1428772 RMVar_hsa_circ_160348,RMVar_hsa_circ_123699,RMVar_hsa_circ_269763 85759 RMVar_ID_85759 Human_SNP_ID_516334927 m1A Human chr12 + 113296047 113296047 113296047 GTGCAGCCCCCGCCGCCCAGCAGCCCCCAGGCAGCCGCCAGCGCTCCCAGACCGTTACCTAGCCC GTGCAGCCCCCGCCGCCCAGCAGCCCCCAGGCGGCCGCCAGCGCTCCCAGACCGTTACCTAGCCC A G TPCN1 Ensembl:ENSG00000186815 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113295960..113296047 26863196 MeRIP-seq:(Medium) rs752033068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19701763,Human_RBP_ID_26322063 Human_Splice_Rec_1428414,Human_Splice_Rec_1428476,Human_Splice_Rec_1428534,Human_Splice_Rec_1428588,Human_Splice_Rec_1428640,Human_Splice_Rec_1428734,Human_Splice_Rec_1428772 RMVar_hsa_circ_160348,RMVar_hsa_circ_123699,RMVar_hsa_circ_269763 85760 RMVar_ID_85760 Human_SNP_ID_516334933 m1A Human chr12 + 113296054 113296054 113296054 CCCCGCCGCCCAGCAGCCCCCAGGCAGCCGCCAGCGCTCCCAGACCGTTACCTAGCCCAGCGCCC CCCCGCCGCCCAGCAGCCCCCAGGCAGCCGCCTGCGCTCCCAGACCGTTACCTAGCCCAGCGCCC A T TPCN1 Ensembl:ENSG00000186815 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:113295971..113296100 26863196 MeRIP-seq:(Medium) rs200966619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19701763,Human_RBP_ID_26322063 Human_Splice_Rec_1428414,Human_Splice_Rec_1428476,Human_Splice_Rec_1428534,Human_Splice_Rec_1428588,Human_Splice_Rec_1428640,Human_Splice_Rec_1428734,Human_Splice_Rec_1428772 RMVar_hsa_circ_160348,RMVar_hsa_circ_123699,RMVar_hsa_circ_269763 85761 RMVar_ID_85761 Human_SNP_ID_516337286 m1A Human chr12 - 113304385 113304385 113304385 ATTCCAGCAAAGCTTCCTGAGCTGGGCTGCAGACATCCTCGTGGGTGTGGGGCTGGGCTGCCTGC ATTCCAGCAAAGCTTCCTGAGCTGGGCTGCAGCCATCCTCGTGGGTGTGGGGCTGGGCTGCCTGC T G SLC8B1 Ensembl:ENSG00000089060 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113304334..113306544 32194978 MeRIP-seq:(Medium) rs757675280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1428800,Human_Splice_Rec_1428801,Human_Splice_Rec_1428828,Human_Splice_Rec_1428829,Human_Splice_Rec_1428844,Human_Splice_Rec_1428845,Human_Splice_Rec_1428864,Human_Splice_Rec_1428865,Human_Splice_Rec_1428872,Human_Splice_Rec_1428873,Human_Splice_Rec_1428876,Human_Splice_Rec_1428877,Human_Splice_Rec_1428900,Human_Splice_Rec_1428901 RMVar_hsa_circ_54881,RMVar_hsa_circ_334390,RMVar_hsa_circ_316078,RMVar_hsa_circ_160353 85762 RMVar_ID_85762 Human_SNP_ID_516340158 m1A Human chr12 - 113315449 113315449 113315449 GACAGCTGCCTGTGGAGTTCCTGCTGCTCCTCACAGTCCCCGTCGTGGACCCGGACAAGGATGAC GACAGCTGCCTGTGGAGTTCCTGCTGCTCCTCCCAGTCCCCGTCGTGGACCCGGACAAGGATGAC T G SLC8B1 Ensembl:ENSG00000089060 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113310321..113316599 32194978 MeRIP-seq:(Medium) rs1566233084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18977869 Human_Splice_Rec_1428792,Human_Splice_Rec_1428820,Human_Splice_Rec_1428836,Human_Splice_Rec_1428856,Human_Splice_Rec_1428892,Human_Splice_Rec_1428918,Human_Splice_Rec_1428930 RMVar_hsa_circ_16906,RMVar_hsa_circ_334390,RMVar_hsa_circ_109565,RMVar_hsa_circ_376109,RMVar_hsa_circ_160354,RMVar_hsa_circ_160355,RMVar_hsa_circ_160356,RMVar_hsa_circ_291640,RMVar_hsa_circ_326750,RMVar_hsa_circ_330011,RMVar_hsa_circ_160357 85763 RMVar_ID_85763 Human_SNP_ID_516341886 m1A Human chr12 + 113321085 113321085 113321085 CACAACTTGGCTGCGGTGACTCCCAGAATCAGAAACAGGTAGAGCAGCCAGGAAACCTGGGTGGG CACAACTTGGCTGCGGTGACTCCCAGAATCAGGAACAGGTAGAGCAGCCAGGAAACCTGGGTGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113320836..113332795 32194978 MeRIP-seq:(Medium) rs1250383809 Functional Loss SNV dbSNP153 33..33 33 - - - 85764 RMVar_ID_85764 Human_SNP_ID_516351182 m1A Human chr12 - 113358650 113358650 113358650 CCAGCACCAGGGCCAGCGCCAGCGCCCGCGTCAGCGCCCGGGCCAGGTGGCTGCCGGGGTAGCAG CCAGCACCAGGGCCAGCGCCAGCGCCCGCGTCGGCGCCCGGGCCAGGTGGCTGCCGGGGTAGCAG T C SLC8B1 Ensembl:ENSG00000089060 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113358607..113358754 26863196 MeRIP-seq:(Medium) rs1371452053 Functional Loss SNV dbSNP153 33..33 33 - - - 85765 RMVar_ID_85765 Human_SNP_ID_516351188 m1A Human chr12 - 113358662 113358656 113358662 CGACCAGCAGGGCCAGCACCAGGGCCAGCGCCAGCGCCCGCGTCAGCGCCCGGGCCAGGTGGCTG CGACCAGCAGGGCCAGCACCAGGGCCAGCGCC______CGCGTCAGCGCCCGGGCCAGGTGGCTG GGGCGCT G SLC8B1 Ensembl:ENSG00000089060 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113358612..113358797 26863196 MeRIP-seq:(Medium) rs774732020 Functional Loss DEL dbSNP153 33..38 33 - - - 85766 RMVar_ID_85766 Human_SNP_ID_516356753 m1A Human chr12 + 113380834 113380834 113380834 TCTTCTCCTGCGACGACTTCTACATCCTGGGCAGTGGGCTGGTGAGTCCCTTTCTCATGTCTCCT TCTTCTCCTGCGACGACTTCTACATCCTGGGCGGTGGGCTGGTGAGTCCCTTTCTCATGTCTCCT A G PLBD2 Ensembl:ENSG00000151176 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113380783..113384145 32194978 MeRIP-seq:(Medium) rs1167509311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11828135 Human_Splice_Rec_1428996,Human_Splice_Rec_1428997,Human_Splice_Rec_1429016,Human_Splice_Rec_1429017 RMVar_hsa_circ_14710,RMVar_hsa_circ_81123,RMVar_hsa_circ_123354,RMVar_hsa_circ_160368,RMVar_hsa_circ_160369,RMVar_hsa_circ_301276,RMVar_hsa_circ_98008,RMVar_hsa_circ_84820,RMVar_hsa_circ_87510,RMVar_hsa_circ_160371,RMVar_hsa_circ_160372,RMVar_hsa_circ_344949,RMVar_hsa_circ_160374,RMVar_hsa_circ_125550,RMVar_hsa_circ_108116,RMVar_hsa_circ_160375,RMVar_hsa_circ_160376,RMVar_hsa_circ_118353,RMVar_hsa_circ_160377,RMVar_hsa_circ_160378 85767 RMVar_ID_85767 Human_SNP_ID_516358755 m1A Human chr12 - 113387902 113387902 113387902 AGCTCAGGCCCTAGGGAGGAGGCAGCACCTTCACATCGATACCCCCATGGGAGCGCTGACGCAGG AGCTCAGGCCCTAGGGAGGAGGCAGCACCTTCGCATCGATACCCCCATGGGAGCGCTGACGCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:113387044..113388499 32194978 MeRIP-seq:(Medium) rs758498982 Functional Loss SNV dbSNP153 33..33 33 - - - 85768 RMVar_ID_85768 Human_SNP_ID_516359429 m1A Human chr12 - 113390324 113390317 113390325 TTGGATGGGTGATTGGATGGATGGATGGGTGGATGGGTGACAAATAGGTAGGTGGATGGGTGGAT TTGGATGGGTGATTGGATGGATGGATGGGTG________ACAAATAGGTAGGTGGATGGGTGGAT TCACCCATC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:113390274..113390422 26863196 MeRIP-seq:(Medium) rs957967330 Functional Loss DEL dbSNP153 32..39 33 - - - 85769 RMVar_ID_85769 Human_SNP_ID_516359635 m1A Human chr12 + 113391155 113391155 113391155 CATATTGTGGTATACAGACAGATACAAAAAAAAAGGCTCTCTCCCTGTCTGATCTCATGCAGCCT CATATTGTGGTATACAGACAGATACAAAAAAAGAGGCTCTCTCCCTGTCTGATCTCATGCAGCCT A G PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs911638436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194985,Human_RBP_ID_259934,Human_RBP_ID_2306617,Human_RBP_ID_4202627,Human_RBP_ID_17075372,Human_RBP_ID_17243004,Human_RBP_ID_17561287,Human_RBP_ID_22170168,Human_RBP_ID_22369790,Human_RBP_ID_24530000,Human_RBP_ID_26412228,Human_RBP_ID_26755649 85770 RMVar_ID_85770 Human_SNP_ID_516367882 m1A Human chr12 - 113422467 113422467 113422467 CAGCTGGCCCCAGACCCCTTACCTCCCTGCCCAACTATCCCAGACCAGCGTGGCCCCAGCTCCTG CAGCTGGCCCCAGACCCCTTACCTCCCTGCCCGACTATCCCAGACCAGCGTGGCCCCAGCTCCTG T C SDS Ensembl:ENSG00000135094 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113422417..113422714 26863196 MeRIP-seq:(Medium) rs891328405 Functional Loss SNV dbSNP153 33..33 33 - - - 85771 RMVar_ID_85771 Human_SNP_ID_516367890 m1A Human chr12 - 113422488 113422488 113422488 CACACTGAGCCCCAGGGGCCCCAGCTGGCCCCAGACCCCTTACCTCCCTGCCCAACTATCCCAGA CACACTGAGCCCCAGGGGCCCCAGCTGGCCCCGGACCCCTTACCTCCCTGCCCAACTATCCCAGA T C SDS Ensembl:ENSG00000135094 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:113422440..113422569 26863196 MeRIP-seq:(Medium) rs1280674037 Functional Loss SNV dbSNP153 33..33 33 - - - 85772 RMVar_ID_85772 Human_SNP_ID_516371046 m1A Human chr12 - 113434098 113434098 113434098 CAGAGAAACCAAGGGCCCTCAGAACAGCCGGGAGTGGGACTGCTATGGAGGCCGGAGCAGAGGCC CAGAGAAACCAAGGGCCCTCAGAACAGCCGGGGGTGGGACTGCTATGGAGGCCGGAGCAGAGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113434097..113434170 26863196 MeRIP-seq:(Medium) rs1407089478 Functional Loss SNV dbSNP153 33..33 33 - - - 85773 RMVar_ID_85773 Human_SNP_ID_516473018 m1A Human chr12 - 113823267 113823267 113823267 TGTGGTGTTGGACGAGATCCTGGAGCAGCTGGAAGGCAGTGACAGCGACAGCGAGGAGCAGACCC TGTGGTGTTGGACGAGATCCTGGAGCAGCTGGGAGGCAGTGACAGCGACAGCGAGGAGCAGACCC T C RBM19 Ensembl:ENSG00000122965 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:113823063..113823266 26863196 MeRIP-seq:(Medium) rs1231748122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875170,Human_RBP_ID_5560891,Human_RBP_ID_6137212,Human_RBP_ID_9365608,Human_RBP_ID_18976233,Human_RBP_ID_22911048,Human_RBP_ID_26323405 Human_Splice_Rec_1429262,Human_Splice_Rec_1429263,Human_Splice_Rec_1429310,Human_Splice_Rec_1429311,Human_Splice_Rec_1429358,Human_Splice_Rec_1429362 RMVar_hsa_circ_160390,RMVar_hsa_circ_93935,RMVar_hsa_circ_106154,RMVar_hsa_circ_116265,RMVar_hsa_circ_121814,RMVar_hsa_circ_160388,RMVar_hsa_circ_77868,RMVar_hsa_circ_87612,RMVar_hsa_circ_160392,RMVar_hsa_circ_160393,RMVar_hsa_circ_160394,RMVar_hsa_circ_160391,RMVar_hsa_circ_88809,RMVar_hsa_circ_160395 85774 RMVar_ID_85774 Human_SNP_ID_516506484 m1A Human chr12 - 113955211 113955211 113955211 GGCCACTTCTGTTTGTTTTTGTGATCACTCAGACAGAGAAACCAGCAAACCAGAAGGAACCCACC GGCCACTTCTGTTTGTTTTTGTGATCACTCAGGCAGAGAAACCAGCAAACCAGAAGGAACCCACC T C RBM19 Ensembl:ENSG00000122965 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:113955186..113955268;chr12:113955188..113955262 26863196 MeRIP-seq:(Medium) rs1566041292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1429228,Human_Splice_Rec_1429229,Human_Splice_Rec_1429276,Human_Splice_Rec_1429277,Human_Splice_Rec_1429324,Human_Splice_Rec_1429325 RMVar_hsa_circ_18309,RMVar_hsa_circ_93935,RMVar_hsa_circ_106154,RMVar_hsa_circ_116265,RMVar_hsa_circ_160388,RMVar_hsa_circ_87612,RMVar_hsa_circ_160392,RMVar_hsa_circ_160393,RMVar_hsa_circ_160394,RMVar_hsa_circ_105623,RMVar_hsa_circ_122373,RMVar_hsa_circ_160399,RMVar_hsa_circ_160401,RMVar_hsa_circ_90170,RMVar_hsa_circ_160400,RMVar_hsa_circ_269375 85775 RMVar_ID_85775 Human_SNP_ID_516509468 m1A Human chr12 - 113966244 113966244 113966244 AAGACGCTGACCAGTCGTGTTGGAATCAAAACAGCGGGGACCCTGCGCCATGTCGCGACTGATCG AAGACGCTGACCAGTCGTGTTGGAATCAAAACGGCGGGGACCCTGCGCCATGTCGCGACTGATCG T C RBM19 Ensembl:ENSG00000122965 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:113966147..113966248 26863196 MeRIP-seq:(Medium) rs1169695023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34437,Human_RBP_ID_4247024,Human_RBP_ID_9365625,Human_RBP_ID_22898935,Human_RBP_ID_26321022 Human_Splice_Rec_1429217,Human_Splice_Rec_1429265,Human_Splice_Rec_1429313 RMVar_hsa_circ_87612,RMVar_hsa_circ_160394,RMVar_hsa_circ_122373,RMVar_hsa_circ_160401 85776 RMVar_ID_85776 Human_SNP_ID_516696597 m1A Human chr12 - 114672173 114672173 114672173 TGCACCGCCACCCCTTCCTCAATCTGAACACCATGCGCCCGCGGCTGCGCTACAGCCCCTACTCC TGCACCGCCACCCCTTCCTCAATCTGAACACCGTGCGCCCGCGGCTGCGCTACAGCCCCTACTCC T C TBX3 Ensembl:ENSG00000135111 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:114672122..114672226 26863196 MeRIP-seq:(Medium) rs1382396799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810490,Human_RBP_ID_11829019,Human_RBP_ID_27418687 RMVar_hsa_circ_105025,RMVar_hsa_circ_120687,RMVar_hsa_circ_160405,RMVar_hsa_circ_160406 85777 RMVar_ID_85777 Human_SNP_ID_516696603 m1A Human chr12 + 114672181 114672181 114672181 GGCTGTAGCGCAGCCGCGGGCGCATGGTGTTCAGATTGAGGAAGGGGTGGCGGTGCACCGAGCTG GGCTGTAGCGCAGCCGCGGGCGCATGGTGTTCGGATTGAGGAAGGGGTGGCGGTGCACCGAGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:114672126..114672325 26863196 MeRIP-seq:(Medium) rs747894358 Functional Loss SNV dbSNP153 33..33 33 - - - 85778 RMVar_ID_85778 Human_SNP_ID_516696648 m1A Human chr12 - 114672251 114672251 114672251 TCGGAAGCCTGTTCCCTTACCCCTACACGTACATGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA TCGGAAGCCTGTTCCCTTACCCCTACACGTACTTGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA T A TBX3 Ensembl:ENSG00000135111 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:114672201..114672250 26863196 MeRIP-seq:(Medium) rs755321111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228939 Human_Splice_Rec_1429492,Human_Splice_Rec_1429504 RMVar_hsa_circ_105025,RMVar_hsa_circ_120687,RMVar_hsa_circ_160405,RMVar_hsa_circ_160406 85779 RMVar_ID_85779 Human_SNP_ID_516696649 m1A Human chr12 - 114672251 114672251 114672251 TCGGAAGCCTGTTCCCTTACCCCTACACGTACATGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA TCGGAAGCCTGTTCCCTTACCCCTACACGTACGTGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA T C TBX3 Ensembl:ENSG00000135111 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:114672201..114672250 26863196 MeRIP-seq:(Medium) rs755321111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228939 Human_Splice_Rec_1429492,Human_Splice_Rec_1429504 RMVar_hsa_circ_105025,RMVar_hsa_circ_120687,RMVar_hsa_circ_160405,RMVar_hsa_circ_160406 85780 RMVar_ID_85780 Human_SNP_ID_516696650 m1A Human chr12 - 114672251 114672251 114672251 TCGGAAGCCTGTTCCCTTACCCCTACACGTACATGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA TCGGAAGCCTGTTCCCTTACCCCTACACGTACCTGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA T G TBX3 Ensembl:ENSG00000135111 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:114672201..114672250 26863196 MeRIP-seq:(Medium) rs755321111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228939 Human_Splice_Rec_1429492,Human_Splice_Rec_1429504 RMVar_hsa_circ_105025,RMVar_hsa_circ_120687,RMVar_hsa_circ_160405,RMVar_hsa_circ_160406 85781 RMVar_ID_85781 Human_SNP_ID_516699997 m1A Human chr12 - 114683666 114683666 114683666 GACAGATAGGGGGCGGGGGAAGAAGAAAAAGAAAGGTAAAAAGTCTTCTAGGAGAACCTTTCACA GACAGATAGGGGGCGGGGGAAGAAGAAAAAGACAGGTAAAAAGTCTTCTAGGAGAACCTTTCACA T G TBX3 Ensembl:ENSG00000135111 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:114683616..114683752 26863196 MeRIP-seq:(Medium) rs1157164898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4250284,Human_RBP_ID_24934511 85782 RMVar_ID_85782 Human_SNP_ID_516700171 m1A Human chr12 + 114684099 114684099 114684099 GAGGGGAGAGAGAGAGAGAGAGAGAGAGACGGAGTCGGAGAGGGAGGGAGCGAGAGAAAGCGAGA GAGGGGAGAGAGAGAGAGAGAGAGAGAGACGGGGTCGGAGAGGGAGGGAGCGAGAGAAAGCGAGA A G AC026765.3 Ensembl:ENSG00000257817 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:114684026..114684155 26863410 MeRIP-seq:(Medium) rs1014454658 Functional Loss SNV dbSNP153 33..33 33 - - - 85783 RMVar_ID_85783 Human_SNP_ID_517020771 m1A Human chr12 - 115986369 115986369 115986369 GCCGTTTTGGGAGAGGCTCTTGTTGGACCCATATGGGGGCCACCGTGATGTTGCCTATATTGTGG GCCGTTTTGGGAGAGGCTCTTGTTGGACCCATTTGGGGGCCACCGTGATGTTGCCTATATTGTGG T A MED13L Ensembl:ENSG00000123066 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:115986318..115986419 32194978 MeRIP-seq:(Medium) rs1190857852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8776443,Human_RBP_ID_9279253,Human_RBP_ID_23539973,Human_RBP_ID_24530221 RMVar_hsa_circ_1572,RMVar_hsa_circ_110209,RMVar_hsa_circ_160409,RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_118763,RMVar_hsa_circ_160413,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_88447,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_160415,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_110434,RMVar_hsa_circ_160420,RMVar_hsa_circ_160421,RMVar_hsa_circ_367442,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_34741,RMVar_hsa_circ_28592,RMVar_hsa_circ_103341,RMVar_hsa_circ_57605,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,RMVar_hsa_circ_160424,RMVar_hsa_circ_92746,RMVar_hsa_circ_82590,RMVar_hsa_circ_160427,RMVar_hsa_circ_160428,RMVar_hsa_circ_119199,RMVar_hsa_circ_160429,RMVar_hsa_circ_160431,RMVar_hsa_circ_87013,RMVar_hsa_circ_160430,RMVar_hsa_circ_127121,RMVar_hsa_circ_160432 85784 RMVar_ID_85784 Human_SNP_ID_517020772 m1A Human chr12 - 115986369 115986369 115986369 GCCGTTTTGGGAGAGGCTCTTGTTGGACCCATATGGGGGCCACCGTGATGTTGCCTATATTGTGG GCCGTTTTGGGAGAGGCTCTTGTTGGACCCATGTGGGGGCCACCGTGATGTTGCCTATATTGTGG T C MED13L Ensembl:ENSG00000123066 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:115986318..115986419 32194978 MeRIP-seq:(Medium) rs1190857852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8776443,Human_RBP_ID_9279253,Human_RBP_ID_23539973,Human_RBP_ID_24530221 RMVar_hsa_circ_1572,RMVar_hsa_circ_110209,RMVar_hsa_circ_160409,RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_118763,RMVar_hsa_circ_160413,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_88447,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_160415,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_110434,RMVar_hsa_circ_160420,RMVar_hsa_circ_160421,RMVar_hsa_circ_367442,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_34741,RMVar_hsa_circ_28592,RMVar_hsa_circ_103341,RMVar_hsa_circ_57605,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,RMVar_hsa_circ_160424,RMVar_hsa_circ_92746,RMVar_hsa_circ_82590,RMVar_hsa_circ_160427,RMVar_hsa_circ_160428,RMVar_hsa_circ_119199,RMVar_hsa_circ_160429,RMVar_hsa_circ_160431,RMVar_hsa_circ_87013,RMVar_hsa_circ_160430,RMVar_hsa_circ_127121,RMVar_hsa_circ_160432 85785 RMVar_ID_85785 Human_SNP_ID_517021508 m1A Human chr12 - 115989386 115989386 115989386 GCGTGAGCCTATCAAGCAGAGAAGGAAGAACCATAGAGGGGGCTTTTGGAAGCCAGGGGTAGCCA GCGTGAGCCTATCAAGCAGAGAAGGAAGAACCGTAGAGGGGGCTTTTGGAAGCCAGGGGTAGCCA T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:115989377..115989447 26863196 MeRIP-seq:(Medium) rs1238656102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1572,RMVar_hsa_circ_110209,RMVar_hsa_circ_160409,RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_118763,RMVar_hsa_circ_160413,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_88447,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_160415,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_110434,RMVar_hsa_circ_160420,RMVar_hsa_circ_160421,RMVar_hsa_circ_367442,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_28592,RMVar_hsa_circ_103341,RMVar_hsa_circ_57605,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,RMVar_hsa_circ_160424,RMVar_hsa_circ_92746,RMVar_hsa_circ_82590,RMVar_hsa_circ_160427,RMVar_hsa_circ_160428,RMVar_hsa_circ_119199,RMVar_hsa_circ_95100,RMVar_hsa_circ_160431,RMVar_hsa_circ_160430,RMVar_hsa_circ_127121,RMVar_hsa_circ_160432,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_160433 85786 RMVar_ID_85786 Human_SNP_ID_517022100 m1A Human chr12 + 115991690 115991687 115991690 GTGGCGGGCTCCACAGAGTTGAGGGGCCGTGTAGTAGAGGGGGTGGAGGCTGGTGATCCTTGATC GTGGCGGGCTCCACAGAGTTGAGGGGCCGT___GTAGAGGGGGTGGAGGCTGGTGATCCTTGATC TGTA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:115991640..115991878 26863196 MeRIP-seq:(Medium) rs1255808844 Functional Loss DEL dbSNP153 31..33 33 - - - 85787 RMVar_ID_85787 Human_SNP_ID_517026179 m1A Human chr12 - 116008426 116008426 116008426 AGGGTGAGAGATGTGATGCCAAAATGGAGGTAAACTCAGAGAGCACTGCATTGCAAAGGTAAGAC AGGGTGAGAGATGTGATGCCAAAATGGAGGTAGACTCAGAGAGCACTGCATTGCAAAGGTAAGAC T C MED13L Ensembl:ENSG00000123066 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:116008407..116008757 32194978 MeRIP-seq:(Medium) rs1182473151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_989875,Human_RBP_ID_1465352,Human_RBP_ID_1787926,Human_RBP_ID_3394442,Human_RBP_ID_8776493,Human_RBP_ID_11829665 Human_Splice_Rec_1429607,Human_Splice_Rec_1429705,Human_Splice_Rec_1429747,Human_Splice_Rec_1429801,Human_Splice_Rec_1429961,Human_Splice_Rec_1430009,Human_Splice_Rec_1430037,Human_Splice_Rec_1430039 Human_miRNA_ID_2645513 RMVar_hsa_circ_110209,RMVar_hsa_circ_160409,RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_118763,RMVar_hsa_circ_160413,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_88447,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_160415,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_110434,RMVar_hsa_circ_160420,RMVar_hsa_circ_160421,RMVar_hsa_circ_367442,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_103341,RMVar_hsa_circ_57605,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,RMVar_hsa_circ_160424,RMVar_hsa_circ_92746,RMVar_hsa_circ_82590,RMVar_hsa_circ_160427,RMVar_hsa_circ_160428,RMVar_hsa_circ_119199,RMVar_hsa_circ_160431,RMVar_hsa_circ_160430,RMVar_hsa_circ_127121,RMVar_hsa_circ_160432,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_45511,RMVar_hsa_circ_334060,RMVar_hsa_circ_371921,RMVar_hsa_circ_160438,RMVar_hsa_circ_91541,RMVar_hsa_circ_160440,RMVar_hsa_circ_4066,RMVar_hsa_circ_119277,RMVar_hsa_circ_61494,RMVar_hsa_circ_99379,RMVar_hsa_circ_160442,RMVar_hsa_circ_160444,RMVar_hsa_circ_108776,RMVar_hsa_circ_160443 85788 RMVar_ID_85788 Human_SNP_ID_517070707 m1A Human chr12 - 116186041 116186041 116186041 CAGAAACGAAGAGGTAGCGTATTTGTTTCAGGAGAAGGGAATAGAATGAATAAAAGCATAGAGAA CAGAAACGAAGAGGTAGCGTATTTGTTTCAGGGGAAGGGAATAGAATGAATAAAAGCATAGAGAA T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:116186038..116186171 26863196 MeRIP-seq:(Medium) rs1259411120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2307447,Human_RBP_ID_9344744,Human_RBP_ID_11831809 RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_160412,RMVar_hsa_circ_160418,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_160421,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_160426,RMVar_hsa_circ_92746,RMVar_hsa_circ_160427,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_119277,RMVar_hsa_circ_160443,RMVar_hsa_circ_100853,RMVar_hsa_circ_97562,RMVar_hsa_circ_160446,RMVar_hsa_circ_160447,RMVar_hsa_circ_160449,RMVar_hsa_circ_105008,RMVar_hsa_circ_160452,RMVar_hsa_circ_76796,RMVar_hsa_circ_286545,RMVar_hsa_circ_119391,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987 85789 RMVar_ID_85789 Human_SNP_ID_517093444 m1A Human chr12 - 116277137 116277137 116277137 GACATGCCCCGCTCTGGCGGCCGGGCTCGCGGAGGATCATGACTGCGGCAGCGAACTGGGTGGCG GACATGCCCCGCTCTGGCGGCCGGGCTCGCGGGGGATCATGACTGCGGCAGCGAACTGGGTGGCG T C MED13L Ensembl:ENSG00000123066 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:116277059..116277227;chr12:116277051..116277227 26863196 MeRIP-seq:(Medium) rs1405857649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229904,Human_RBP_ID_811590,Human_RBP_ID_3942211,Human_RBP_ID_4246333,Human_RBP_ID_8776529,Human_RBP_ID_9279257,Human_RBP_ID_18188899,Human_RBP_ID_18977896,Human_RBP_ID_22910798 Human_Splice_Rec_1429589,Human_Splice_Rec_1429687,Human_Splice_Rec_1430057 Human_miRNA_ID_2617792 RMVar_hsa_circ_119391,RMVar_hsa_circ_160455,RMVar_hsa_circ_114989,RMVar_hsa_circ_160465 85790 RMVar_ID_85790 Human_SNP_ID_517093462 m1A Human chr12 + 116277172 116277172 116277172 GCGAGCCCGGCCGCCAGAGCGGGGCATGTCGGAGCGAGGCGTCCGAGGCGAGGCCGGGCCGGGCG GCGAGCCCGGCCGCCAGAGCGGGGCATGTCGGGGCGAGGCGTCCGAGGCGAGGCCGGGCCGGGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:116277140..116277284 26863196 MeRIP-seq:(Medium) rs889781088 Functional Loss SNV dbSNP153 33..33 33 - - - 85791 RMVar_ID_85791 Human_SNP_ID_517093572 m1A Human chr12 - 116277424 116277400 116277424 AGTCGGTGGCTGGAGATAAACAAGGCGGCGGCAGCGGCAGCAGCGGCGGCGGCGGCGGCTGAGGA AGTCGGTGGCTGGAGATAAACAAGGCGGCGGC________________________GGCTGAGGA CGCCGCCGCCGCCGCTGCTGCCGCT C MED13L Ensembl:ENSG00000123066 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr12:116277376..116277604;chr12:116277344..116277629 26863196 MeRIP-seq:(Medium) rs943317638 Functional Loss DEL dbSNP153 33..56 33 - - - 85792 RMVar_ID_85792 Human_SNP_ID_517093587 m1A Human chr12 - 116277424 116277424 116277424 AGTCGGTGGCTGGAGATAAACAAGGCGGCGGCAGCGGCAGCAGCGGCGGCGGCGGCGGCTGAGGA AGTCGGTGGCTGGAGATAAACAAGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCTGAGGA T C MED13L Ensembl:ENSG00000123066 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr12:116277376..116277604;chr12:116277344..116277629 26863196 MeRIP-seq:(Medium) rs1008607514 Functional Loss SNV dbSNP153 33..33 33 - - - 85793 RMVar_ID_85793 Human_SNP_ID_517093591 m1A Human chr12 - 116277437 116277433 116277437 GGGGCCGAGGGGGAGTCGGTGGCTGGAGATAAACAAGGCGGCGGCAGCGGCAGCAGCGGCGGCGG GGGGCCGAGGGGGAGTCGGTGGCTGGAGATAA____GGCGGCGGCAGCGGCAGCAGCGGCGGCGG CTTGT C MED13L Ensembl:ENSG00000123066 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:116277333..116277675;chr12:116277351..116277650 26863196 MeRIP-seq:(Medium) rs1379037260 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_17810295 85794 RMVar_ID_85794 Human_SNP_ID_517093602 m1A Human chr12 - 116277462 116277462 116277462 GCTCGCCTCCCCTCGCGCGCCGGCGGGGGCCGAGGGGGAGTCGGTGGCTGGAGATAAACAAGGCG GCTCGCCTCCCCTCGCGCGCCGGCGGGGGCCGGGGGGGAGTCGGTGGCTGGAGATAAACAAGGCG T C MED13L Ensembl:ENSG00000123066 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:116277378..116277612 26863196 MeRIP-seq:(Medium) rs1246249833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8776531 85795 RMVar_ID_85795 Human_SNP_ID_517093615 m1A Human chr12 + 116277500 116277500 116277500 CCCGCCGGCGCGCGAGGGGAGGCGAGCCCCGGAGCCGCCGCCGCCGCCTCGGAGCCGCCGCCGCC CCCGCCGGCGCGCGAGGGGAGGCGAGCCCCGGGGCCGCCGCCGCCGCCTCGGAGCCGCCGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:116277076..116277670 26863196 MeRIP-seq:(Medium) rs1228688906 Functional Loss SNV dbSNP153 33..33 33 - - - 85796 RMVar_ID_85796 Human_SNP_ID_517093666 m1A Human chr12 + 116277599 116277599 116277599 CGAAGCCAGCGGGCGACCCCGGCAGCCGAGCGACGTCCCCTCCTTCCTCTTCCTCCCCCACCCCC CGAAGCCAGCGGGCGACCCCGGCAGCCGAGCGGCGTCCCCTCCTTCCTCTTCCTCCCCCACCCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:116277376..116277650 26863196 MeRIP-seq:(Medium) rs1216161228 Functional Loss SNV dbSNP153 33..33 33 - - - 85797 RMVar_ID_85797 Human_SNP_ID_517159239 m1A Human chr12 - 116534081 116534081 116534081 GAGTAGATACATTCGGGAAAACCTGGGGGGAGAAGGAGGAGGAGGAGGGGAGGAGCGTGTGCAGG GAGTAGATACATTCGGGAAAACCTGGGGGGAGGAGGAGGAGGAGGAGGGGAGGAGCGTGTGCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:116534031..116534141 26863196 MeRIP-seq:(Medium) rs747198820 Functional Loss SNV dbSNP153 33..33 33 - - - 85798 RMVar_ID_85798 Human_SNP_ID_517205454 m1A Human chr12 + 116720272 116720272 116720272 TAAAACAGAGGCCGAAAGAAAAAAGGAGCCGCAGAACCAGGATCAACTCCCCATACCTTGTTGGG TAAAACAGAGGCCGAAAGAAAAAAGGAGCCGCCGAACCAGGATCAACTCCCCATACCTTGTTGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:116720266..116720364 26863196 MeRIP-seq:(Medium) rs780903919 Functional Loss SNV dbSNP153 33..33 33 - - - 85799 RMVar_ID_85799 Human_SNP_ID_517205455 m1A Human chr12 + 116720272 116720272 116720272 TAAAACAGAGGCCGAAAGAAAAAAGGAGCCGCAGAACCAGGATCAACTCCCCATACCTTGTTGGG TAAAACAGAGGCCGAAAGAAAAAAGGAGCCGCGGAACCAGGATCAACTCCCCATACCTTGTTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:116720266..116720364 26863196 MeRIP-seq:(Medium) rs780903919 Functional Loss SNV dbSNP153 33..33 33 - - - 85800 RMVar_ID_85800 Human_SNP_ID_517209631 m1A Human chr12 + 116737876 116737876 116737876 GAGCACCCACCTCTTCCGCAGAAGCCGGCGCCACACCATGGCCGCCAGGTTCACCATCCCGGCGC GAGCACCCACCTCTTCCGCAGAAGCCGGCGCCGCACCATGGCCGCCAGGTTCACCATCCCGGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:116737826..116738037 26863196 MeRIP-seq:(Medium) rs766670718 Functional Loss SNV dbSNP153 33..33 33 - - - 85801 RMVar_ID_85801 Human_SNP_ID_517209634 m1A Human chr12 - 116737882 116737882 116737882 ACGTCCGCGCCGGGATGGTGAACCTGGCGGCCATGGTGTGGCGCCGGCTTCTGCGGAAGAGGTGG ACGTCCGCGCCGGGATGGTGAACCTGGCGGCCGTGGTGTGGCGCCGGCTTCTGCGGAAGAGGTGG T C C12orf49 Ensembl:ENSG00000111412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:116737832..116738016 26863196 MeRIP-seq:(Medium) rs557048187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_411572,Human_RBP_ID_4203232,Human_RBP_ID_5437309 Human_Splice_Rec_1430131,Human_Splice_Rec_1430139,Human_Splice_Rec_1430147 85802 RMVar_ID_85802 Human_SNP_ID_517222632 m1A Human chr12 + 116789670 116789670 116789670 GATGGATGGATGGATGGATGGATGGATGGATAAATGGGAGGAGAGTAGAGGGATGGATGGGTGGA GATGGATGGATGGATGGATGGATGGATGGATAGATGGGAGGAGAGTAGAGGGATGGATGGGTGGA A G RNFT2 Ensembl:ENSG00000135119 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:116789649..116789862 26863196 MeRIP-seq:(Medium) rs1185566323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5644683 RMVar_hsa_circ_99691,RMVar_hsa_circ_160473,RMVar_hsa_circ_335007,RMVar_hsa_circ_32465,RMVar_hsa_circ_160479,RMVar_hsa_circ_49188,RMVar_hsa_circ_160481 85803 RMVar_ID_85803 Human_SNP_ID_517234731 m1A Human chr12 - 116839528 116839528 116839528 TTGCCCATCCATACAGTCACTCACCCCCTTATACCTCTGTCCACCTACCGTTCACTCACCCACCA TTGCCCATCCATACAGTCACTCACCCCCTTATTCCTCTGTCCACCTACCGTTCACTCACCCACCA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:116839484..116839630 26863196 MeRIP-seq:(Medium) rs1430045809 Functional Loss SNV dbSNP153 33..33 33 - - - 85804 RMVar_ID_85804 Human_SNP_ID_517245472 m1A Human chr12 - 116881413 116881413 116881413 AAACGCACAACACAAGGAGAAACTTGGTGTCCAGGGGAGGCCCCCGGCGGCTGGAGCGCGGCGGC AAACGCACAACACAAGGAGAAACTTGGTGTCCTGGGGAGGCCCCCGGCGGCTGGAGCGCGGCGGC T A HRK Ensembl:ENSG00000135116 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:116881352..116881441;chr12:116881256..116881423 26863196 MeRIP-seq:(Medium) rs564574409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203441 85805 RMVar_ID_85805 Human_SNP_ID_517245473 m1A Human chr12 - 116881413 116881413 116881413 AAACGCACAACACAAGGAGAAACTTGGTGTCCAGGGGAGGCCCCCGGCGGCTGGAGCGCGGCGGC AAACGCACAACACAAGGAGAAACTTGGTGTCCGGGGGAGGCCCCCGGCGGCTGGAGCGCGGCGGC T C HRK Ensembl:ENSG00000135116 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:116881352..116881441;chr12:116881256..116881423 26863196 MeRIP-seq:(Medium) rs564574409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203441 85806 RMVar_ID_85806 Human_SNP_ID_517252905 m1A Human chr12 - 116911054 116911054 116911054 GCTCCTCCTGCCAGCGCCGACGGAACTCATCCAGGCTGTAGTCGTCCATATTCGCCGCTCCCGGC GCTCCTCCTGCCAGCGCCGACGGAACTCATCCTGGCTGTAGTCGTCCATATTCGCCGCTCCCGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:116911005..116911304 32194978 MeRIP-seq:(Medium) rs774166467 Functional Loss SNV dbSNP153 33..33 33 - - - 85807 RMVar_ID_85807 Human_SNP_ID_517252909 m1A Human chr12 + 116911060 116911060 116911060 AGCGGCGAATATGGACGACTACAGCCTGGATGAGTTCCGTCGGCGCTGGCAGGAGGAGCTGGCGC AGCGGCGAATATGGACGACTACAGCCTGGATGGGTTCCGTCGGCGCTGGCAGGAGGAGCTGGCGC A G FBXW8 Ensembl:ENSG00000174989 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:116911009..116911168 26863196 MeRIP-seq:(Medium) rs1448359554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203455,Human_RBP_ID_9322721,Human_RBP_ID_11834027,Human_RBP_ID_18977898,Human_RBP_ID_22170275,Human_RBP_ID_22910911,Human_RBP_ID_27806059 Human_Splice_Rec_1430297 85808 RMVar_ID_85808 Human_SNP_ID_517270682 m1A Human chr12 + 116988820 116988820 116988820 GCCTGTCACATGTCTAGACGTCTCGGCCAACCAAGTTGCTTTTGGTGTACAGGGTCTGGGATGGG GCCTGTCACATGTCTAGACGTCTCGGCCAACCGAGTTGCTTTTGGTGTACAGGGTCTGGGATGGG A G FBXW8 Ensembl:ENSG00000174989 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:116988774..117010328 32194978 MeRIP-seq:(Medium) rs1192999072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1430289,Human_Splice_Rec_1430309,Human_Splice_Rec_1430329 RMVar_hsa_circ_107592,RMVar_hsa_circ_160489,RMVar_hsa_circ_353757,RMVar_hsa_circ_288492,RMVar_hsa_circ_160498,RMVar_hsa_circ_160499,RMVar_hsa_circ_160502,RMVar_hsa_circ_334919,RMVar_hsa_circ_291040,RMVar_hsa_circ_293302,RMVar_hsa_circ_22540,RMVar_hsa_circ_160505,RMVar_hsa_circ_287004,RMVar_hsa_circ_160504,RMVar_hsa_circ_278518,RMVar_hsa_circ_160508,RMVar_hsa_circ_160509 85809 RMVar_ID_85809 Human_SNP_ID_517280325 m1A Human chr12 + 117028069 117028069 117028069 GCTGATCCGCGCCTATGAGTTTGCGGTGGACCAGCTGGCCTTCCAGAGCCCTCTCCCTGTCTGCC GCTGATCCGCGCCTATGAGTTTGCGGTGGACCCGCTGGCCTTCCAGAGCCCTCTCCCTGTCTGCC A C FBXW8 Ensembl:ENSG00000174989 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:117028066..117028166 32194978 MeRIP-seq:(Medium) rs779815951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8366758 Human_Splice_Rec_1430296,Human_Splice_Rec_1430316,Human_Splice_Rec_1430336 85810 RMVar_ID_85810 Human_SNP_ID_517281267 m1A Human chr12 + 117031504 117031504 117031504 GGGAGACCGAGGCAGGCGTATCACCTGAGGTCAGGAGCTCAAGACCAGCCTGGCCAACATGGCAA GGGAGACCGAGGCAGGCGTATCACCTGAGGTCTGGAGCTCAAGACCAGCCTGGCCAACATGGCAA A T - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1163401140 Functional Loss SNV dbSNP153 33..33 33 - - - 85811 RMVar_ID_85811 Human_SNP_ID_517299357 m1A Human chr12 - 117099285 117099285 117099285 GGGACGCGCGCCCCGGGGCCCCCGCCGCGGGCACCATGGGCGCTGCCCACTCCGCGTCTGAGGAG GGGACGCGCGCCCCGGGGCCCCCGCCGCGGGCGCCATGGGCGCTGCCCACTCCGCGTCTGAGGAG T C TESC Ensembl:ENSG00000088992 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:117099261..117099367 26863196 MeRIP-seq:(Medium) rs1440104563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246340,Human_RBP_ID_22437444 Human_Splice_Rec_1430345,Human_Splice_Rec_1430359,Human_Splice_Rec_1430373,Human_Splice_Rec_1430389,Human_Splice_Rec_1430407 85812 RMVar_ID_85812 Human_SNP_ID_517299358 m1A Human chr12 - 117099285 117099285 117099285 GGGACGCGCGCCCCGGGGCCCCCGCCGCGGGCACCATGGGCGCTGCCCACTCCGCGTCTGAGGAG GGGACGCGCGCCCCGGGGCCCCCGCCGCGGGCCCCATGGGCGCTGCCCACTCCGCGTCTGAGGAG T G TESC Ensembl:ENSG00000088992 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:117099261..117099367 26863196 MeRIP-seq:(Medium) rs1440104563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246340,Human_RBP_ID_22437444 Human_Splice_Rec_1430345,Human_Splice_Rec_1430359,Human_Splice_Rec_1430373,Human_Splice_Rec_1430389,Human_Splice_Rec_1430407 85813 RMVar_ID_85813 Human_SNP_ID_517316026 m1A Human chr12 - 117162586 117162586 117162586 ATCAGCCGCCTTGGTCACTGTCACAGTAATGCAGGGTTATGACGGCTGTATGGACATAGAGAGGG ATCAGCCGCCTTGGTCACTGTCACAGTAATGCGGGGTTATGACGGCTGTATGGACATAGAGAGGG T C FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:117162584..117162696 26863196 MeRIP-seq:(Medium) rs1277182559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11835274 RMVar_hsa_circ_107764,RMVar_hsa_circ_376166,RMVar_hsa_circ_160515,RMVar_hsa_circ_77206,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_160516 85814 RMVar_ID_85814 Human_SNP_ID_517323197 m1A Human chr12 + 117190386 117190386 117190386 CCGGCAGGTTGACGAGGCAGCTGAGGCCCGCTACCTCCGGCGCGGCCTCCTCCGCCAGCGCCGGC CCGGCAGGTTGACGAGGCAGCTGAGGCCCGCTGCCTCCGGCGCGGCCTCCTCCGCCAGCGCCGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:117190296..117190413 26863410 MeRIP-seq:(Medium) rs1427796599 Functional Loss SNV dbSNP153 33..33 33 - - - 85815 RMVar_ID_85815 Human_SNP_ID_517323225 m1A Human chr12 - 117190429 117190429 117190429 ACAAGATGGCGGCGGCAGCAGTCGACAGCGCGATGGAGGTGGTGCCGGCGCTGGCGGAGGAGGCC ACAAGATGGCGGCGGCAGCAGTCGACAGCGCGTTGGAGGTGGTGCCGGCGCTGGCGGAGGAGGCC T A FBXO21 Ensembl:ENSG00000135108 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:117190275..117190493;chr12:117190316..117190448 26863196 MeRIP-seq:(Medium) rs1358558857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203612,Human_RBP_ID_18977905,Human_RBP_ID_23540973 85816 RMVar_ID_85816 Human_SNP_ID_517323226 m1A Human chr12 - 117190429 117190429 117190429 ACAAGATGGCGGCGGCAGCAGTCGACAGCGCGATGGAGGTGGTGCCGGCGCTGGCGGAGGAGGCC ACAAGATGGCGGCGGCAGCAGTCGACAGCGCGGTGGAGGTGGTGCCGGCGCTGGCGGAGGAGGCC T C FBXO21 Ensembl:ENSG00000135108 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:117190275..117190493;chr12:117190316..117190448 26863196 MeRIP-seq:(Medium) rs1358558857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203612,Human_RBP_ID_18977905,Human_RBP_ID_23540973 85817 RMVar_ID_85817 Human_SNP_ID_517525711 m1A Human chr12 - 118016837 118016837 118016837 CGCCGCGGGCTGCTCCTGCTGCTTGAGTGCTGAGGTCTCCATGGCGGGGAGACGAAGGTGACCAG CGCCGCGGGCTGCTCCTGCTGCTTGAGTGCTGCGGTCTCCATGGCGGGGAGACGAAGGTGACCAG T G lnc-WSB2-3 RNACentral:URS00008B7B9C lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:118016736..118016838 26863410 MeRIP-seq:(Medium) rs772023840 Functional Loss SNV dbSNP153 33..33 33 - - - 85818 RMVar_ID_85818 Human_SNP_ID_517528337 m1A Human chr12 - 118026904 118026904 118026904 GGTGTAGACAGTCTCCTCTGTCACCTTCCCAAAGGCCATATTGGTGCTCTGTGTAGACAGAGGGG GGTGTAGACAGTCTCCTCTGTCACCTTCCCAAGGGCCATATTGGTGCTCTGTGTAGACAGAGGGG T C lnc-WSB2-3 RNACentral:URS00008B7B9C lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:118024902..118027049 32194978 MeRIP-seq:(Medium) rs772892553 Functional Loss SNV dbSNP153 33..33 33 - - - 85819 RMVar_ID_85819 Human_SNP_ID_517529408 m1A Human chr12 + 118031396 118031395 118031396 CTGTGGGATGAATCAGTCACCCCGAATCTTGGAAAAACCCCCTTCCAGGAGAGGATGGGCAGGCA CTGTGGGATGAATCAGTCACCCCGAATCTTGG_AAAACCCCCTTCCAGGAGAGGATGGGCAGGCA GA G RFC5 Ensembl:ENSG00000111445 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:118031204..118031705 32194978 MeRIP-seq:(Medium) rs1427690936 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_411731,Human_RBP_ID_17357746,Human_RBP_ID_17810538,Human_RBP_ID_23207861,Human_RBP_ID_23541075 RMVar_hsa_circ_19318,RMVar_hsa_circ_21703 85820 RMVar_ID_85820 Human_SNP_ID_517530294 m1A Human chr12 + 118035060 118035060 118035060 AGCCCATTGGTCATAGGAGCAAATGCAATGGGAGTTTTCAGTTCCAGGGCCCAGATCCTGAGGAG AGCCCATTGGTCATAGGAGCAAATGCAATGGGCGTTTTCAGTTCCAGGGCCCAGATCCTGAGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:118035010..118035090 26863196 MeRIP-seq:(Medium) rs764416783 Functional Loss SNV dbSNP153 33..33 33 - - - 85821 RMVar_ID_85821 Human_SNP_ID_517530350 m1A Human chr12 - 118035249 118035249 118035249 ATTAGCTCACTGAGATCTGTGTGCTTCTCTCCAGAAGGCTTGTACCTTGCCACGGTGGCAGATGA ATTAGCTCACTGAGATCTGTGTGCTTCTCTCCGGAAGGCTTGTACCTTGCCACGGTGGCAGATGA T C WSB2 Ensembl:ENSG00000176871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9788041 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17810572 Human_Splice_Rec_1430962,Human_Splice_Rec_1430963,Human_Splice_Rec_1430978,Human_Splice_Rec_1430979,Human_Splice_Rec_1430994,Human_Splice_Rec_1430995,Human_Splice_Rec_1431006,Human_Splice_Rec_1431007,Human_Splice_Rec_1431020,Human_Splice_Rec_1431021,Human_Splice_Rec_1431036,Human_Splice_Rec_1431042,Human_Splice_Rec_1431043 Human_miRNA_ID_425520,Human_miRNA_ID_817483,Human_miRNA_ID_1261195,Human_miRNA_ID_1374285,Human_miRNA_ID_2136956,Human_miRNA_ID_2609599,Human_miRNA_ID_2665746,Human_miRNA_ID_2793077 GWAS_ID_10205,GWAS_ID_10206,GWAS_ID_10207,GWAS_ID_10208 RMVar_hsa_circ_14306,RMVar_hsa_circ_314695,RMVar_hsa_circ_160544,RMVar_hsa_circ_372187,RMVar_hsa_circ_26822,RMVar_hsa_circ_160545,RMVar_hsa_circ_160546,RMVar_hsa_circ_160547 85822 RMVar_ID_85822 Human_SNP_ID_517531120 m1A Human chr12 - 118038335 118038335 118038335 CGGGCCACCTGCAGTGGGTTTACTGCTGTTCCATCTCCCCAGACTGCAGCATGCTGTGCTCTGCA CGGGCCACCTGCAGTGGGTTTACTGCTGTTCCGTCTCCCCAGACTGCAGCATGCTGTGCTCTGCA T C WSB2 Ensembl:ENSG00000176871 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:118036508..118042502 32194978 MeRIP-seq:(Medium) rs1313613625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_989954,Human_RBP_ID_8776712,Human_RBP_ID_17236387,Human_RBP_ID_17352071,Human_RBP_ID_23541124 Human_Splice_Rec_1430958,Human_Splice_Rec_1430959,Human_Splice_Rec_1430974,Human_Splice_Rec_1430975,Human_Splice_Rec_1430990,Human_Splice_Rec_1430991,Human_Splice_Rec_1431002,Human_Splice_Rec_1431003,Human_Splice_Rec_1431016,Human_Splice_Rec_1431017,Human_Splice_Rec_1431032,Human_Splice_Rec_1431033,Human_Splice_Rec_1431038,Human_Splice_Rec_1431039,Human_Splice_Rec_1431060,Human_Splice_Rec_1431061 RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_314695,RMVar_hsa_circ_160546,RMVar_hsa_circ_305785,RMVar_hsa_circ_271036,RMVar_hsa_circ_160548,RMVar_hsa_circ_160549,RMVar_hsa_circ_160551,RMVar_hsa_circ_106798,RMVar_hsa_circ_377956,RMVar_hsa_circ_160550 85823 RMVar_ID_85823 Human_SNP_ID_517534441 m1A Human chr12 - 118052474 118052474 118052474 GTTTGAAGCATGTTGTCTCCTGCCCCAGAGGAACCGCTGCTGCTGGCCGAACTCAAGCCCGGGCG GTTTGAAGCATGTTGTCTCCTGCCCCAGAGGAGCCGCTGCTGCTGGCCGAACTCAAGCCCGGGCG T C WSB2 Ensembl:ENSG00000176871 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:118052437..118052537 26863410 MeRIP-seq:(Medium) rs1379075563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875213,Human_RBP_ID_4247875,Human_RBP_ID_5490970,Human_RBP_ID_22645430 Human_Splice_Rec_1430956,Human_Splice_Rec_1430968,Human_Splice_Rec_1430984,Human_Splice_Rec_1431000,Human_Splice_Rec_1431026,Human_Splice_Rec_1431046,Human_Splice_Rec_1431054,Human_Splice_Rec_1431064,Human_Splice_Rec_1431070 Human_miRNA_ID_2100973,Human_miRNA_ID_2106927,Human_miRNA_ID_2112870,Human_miRNA_ID_2165415,Human_miRNA_ID_2596662,Human_miRNA_ID_2739570,Human_miRNA_ID_2756719,Human_miRNA_ID_3040170 RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_22776,RMVar_hsa_circ_106798,RMVar_hsa_circ_160550 85824 RMVar_ID_85824 Human_SNP_ID_517534442 m1A Human chr12 - 118052474 118052474 118052474 GTTTGAAGCATGTTGTCTCCTGCCCCAGAGGAACCGCTGCTGCTGGCCGAACTCAAGCCCGGGCG GTTTGAAGCATGTTGTCTCCTGCCCCAGAGGACCCGCTGCTGCTGGCCGAACTCAAGCCCGGGCG T G WSB2 Ensembl:ENSG00000176871 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:118052437..118052537 26863410 MeRIP-seq:(Medium) rs1379075563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875213,Human_RBP_ID_4247875,Human_RBP_ID_5490970,Human_RBP_ID_22645430 Human_Splice_Rec_1430956,Human_Splice_Rec_1430968,Human_Splice_Rec_1430984,Human_Splice_Rec_1431000,Human_Splice_Rec_1431026,Human_Splice_Rec_1431046,Human_Splice_Rec_1431054,Human_Splice_Rec_1431064,Human_Splice_Rec_1431070 Human_miRNA_ID_2100973,Human_miRNA_ID_2106927,Human_miRNA_ID_2112870,Human_miRNA_ID_2165415,Human_miRNA_ID_2596662,Human_miRNA_ID_2739570,Human_miRNA_ID_2756719,Human_miRNA_ID_3040170 RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_22776,RMVar_hsa_circ_106798,RMVar_hsa_circ_160550 85825 RMVar_ID_85825 Human_SNP_ID_517536560 m1A Human chr12 - 118061088 118061074 118061088 GGCGGCATGAGGGCCCGCGGCCCGGGGGGCTGAGGCGCCCGCCGCCTGCCGCGGGGGCCGCTCGC GGCGGCATGAGGGCCCGCGGCCCGGGGGGCTG______________TGCCGCGGGGGCCGCTCGC AGGCGGCGGGCGCCT A WSB2 Ensembl:ENSG00000176871 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:118060995..118061150;chr12:118060981..118061150 26863196 MeRIP-seq:(Medium) rs1320951502 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_4246342,Human_RBP_ID_9322726,Human_RBP_ID_9352776 Human_Splice_Rec_1430955,Human_Splice_Rec_1430967,Human_Splice_Rec_1430999,Human_Splice_Rec_1431025,Human_Splice_Rec_1431045,Human_Splice_Rec_1431063 85826 RMVar_ID_85826 Human_SNP_ID_517536757 m1A Human chr12 + 118061632 118061632 118061632 AGAGCCGGGCTGAGAGAAAAACCAAGCAGGGGAAGCGGCGATCCGGGGAGAACGGAGAGAGGGAG AGAGCCGGGCTGAGAGAAAAACCAAGCAGGGGGAGCGGCGATCCGGGGAGAACGGAGAGAGGGAG A G lnc-RFC5-5 RNACentral:URS0000D59E62 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:118061208..118062122 26863196 MeRIP-seq:(Medium) rs1026619320 Functional Loss SNV dbSNP153 33..33 33 - - - 85827 RMVar_ID_85827 Human_SNP_ID_517538734 m1A Human chr12 - 118068478 118068476 118068479 AGGGGAACAGGAGGGAGCACGTGAGAGAGAGGAGTTGCCAAAAGAAATACCTAAGCAGGACCACA AGGGGAACAGGAGGGAGCACGTGAGAGAGAG___TTGCCAAAAGAAATACCTAAGCAGGACCACA ACTC A VSIG10 Ensembl:ENSG00000176834 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:118068428..118068562 26863196 MeRIP-seq:(Medium) rs770840994 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_95409,RMVar_hsa_circ_86207,RMVar_hsa_circ_104975,RMVar_hsa_circ_160555,RMVar_hsa_circ_160556,RMVar_hsa_circ_160557 85828 RMVar_ID_85828 Human_SNP_ID_517539173 m1A Human chr12 - 118069935 118069935 118069935 GGAGGCATCAGTGTGGTGTAGTAGGAAAAGGCACTGAGACCATTGGACCTGGGTTCAAATGACAG GGAGGCATCAGTGTGGTGTAGTAGGAAAAGGCGCTGAGACCATTGGACCTGGGTTCAAATGACAG T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:118069924..118070042 26863196 MeRIP-seq:(Medium) rs1277940859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95409,RMVar_hsa_circ_86207,RMVar_hsa_circ_104975,RMVar_hsa_circ_160555,RMVar_hsa_circ_160556,RMVar_hsa_circ_160557 85829 RMVar_ID_85829 Human_SNP_ID_517556942 m1A Human chr12 - 118136169 118136169 118136169 CAAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTAGGCCAGGCGCGGGCGACAGAGGCGACGCGGAG CAAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTGGGCCAGGCGCGGGCGACAGAGGCGACGCGGAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:118136101..118136300 26863196 MeRIP-seq:(Medium) rs1375676196 Functional Loss SNV dbSNP153 33..33 33 - - - 85830 RMVar_ID_85830 Human_SNP_ID_517556946 m1A Human chr12 + 118136178 118136178 118136178 GCCTCTGTCGCCCGCGCCTGGCCTACCGCGGCACTCCCGGCTGCACGCTCTGCTTGGCCTCGCCA GCCTCTGTCGCCCGCGCCTGGCCTACCGCGGCGCTCCCGGCTGCACGCTCTGCTTGGCCTCGCCA A G PEBP1 Ensembl:ENSG00000089220 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:118136101..118136375;chr12:118136076..118136451;chr12:118136101..118136429 26863196 MeRIP-seq:(Medium) rs1261585014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228554,Human_RBP_ID_411834,Human_RBP_ID_753089,Human_RBP_ID_809747,Human_RBP_ID_1465586,Human_RBP_ID_4203873,Human_RBP_ID_5314674,Human_RBP_ID_5416700,Human_RBP_ID_5437317,Human_RBP_ID_5461445,Human_RBP_ID_5490973,Human_RBP_ID_8247484,Human_RBP_ID_8366862,Human_RBP_ID_9012011,Human_RBP_ID_9322727,Human_RBP_ID_11836488,Human_RBP_ID_22436713,Human_RBP_ID_22492400,Human_RBP_ID_27418880,Human_RBP_ID_27557646 Human_miRNA_ID_2515833 RMVar_hsa_circ_121207,RMVar_hsa_circ_160564 85831 RMVar_ID_85831 Human_SNP_ID_517556957 m1A Human chr12 - 118136200 118136200 118136200 CACTTGCTGAGGTCCACCGGCATGGCGAGGCCAAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTAG CACTTGCTGAGGTCCACCGGCATGGCGAGGCCCAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTAG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:118136101..118138075 26863410 MeRIP-seq:(Medium) rs1350133769 Functional Loss SNV dbSNP153 33..33 33 - - - 85832 RMVar_ID_85832 Human_SNP_ID_517556974 m1A Human chr12 - 118136231 118136231 118136231 GTCCACTTCTTGCAGGCTCAAGGGCCCGGACCACTTGCTGAGGTCCACCGGCATGGCGAGGCCAA GTCCACTTCTTGCAGGCTCAAGGGCCCGGACCTCTTGCTGAGGTCCACCGGCATGGCGAGGCCAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:118136126..118136350 26863196 MeRIP-seq:(Medium) rs1049582379 Functional Loss SNV dbSNP153 33..33 33 - - - 85833 RMVar_ID_85833 Human_SNP_ID_517556975 m1A Human chr12 - 118136231 118136231 118136231 GTCCACTTCTTGCAGGCTCAAGGGCCCGGACCACTTGCTGAGGTCCACCGGCATGGCGAGGCCAA GTCCACTTCTTGCAGGCTCAAGGGCCCGGACCGCTTGCTGAGGTCCACCGGCATGGCGAGGCCAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:118136126..118136350 26863196 MeRIP-seq:(Medium) rs1049582379 Functional Loss SNV dbSNP153 33..33 33 - - - 85834 RMVar_ID_85834 Human_SNP_ID_517557511 m1A Human chr12 - 118138047 118138047 118138047 TCAAGACCATCCCACGAAATGCTGGTGGGTCTATTCTTAACCTGTATGAAGGAACCAGTTTGCAG TCAAGACCATCCCACGAAATGCTGGTGGGTCTGTTCTTAACCTGTATGAAGGAACCAGTTTGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:118138026..118138050 26863196 MeRIP-seq:(Medium) rs1166092275 Functional Loss SNV dbSNP153 33..33 33 - - - 85835 RMVar_ID_85835 Human_SNP_ID_517557529 m1A Human chr12 + 118138088 118138088 118138088 CAGCATTTCGTGGGATGGTCTTGATTCAGGGAAGCTCTACACCTTGGTCCTGACAGACCCGGATG CAGCATTTCGTGGGATGGTCTTGATTCAGGGAGGCTCTACACCTTGGTCCTGACAGACCCGGATG A G PEBP1 Ensembl:ENSG00000089220 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:118137975..118138175 26863196 MeRIP-seq:(Medium) rs779234877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_411840,Human_RBP_ID_1356218,Human_RBP_ID_1465590,Human_RBP_ID_9012013,Human_RBP_ID_11836498,Human_RBP_ID_17830579,Human_RBP_ID_22437449,Human_RBP_ID_22756150,Human_RBP_ID_26901735 Human_Splice_Rec_1431132,Human_Splice_Rec_1431133 Human_miRNA_ID_2697479,Human_miRNA_ID_3001599 RMVar_hsa_circ_110913,RMVar_hsa_circ_121207,RMVar_hsa_circ_374555,RMVar_hsa_circ_160564,RMVar_hsa_circ_301584,RMVar_hsa_circ_160565,RMVar_hsa_circ_160566,RMVar_hsa_circ_160567 85836 RMVar_ID_85836 Human_SNP_ID_517559289 m1A Human chr12 - 118144599 118144599 118144599 AGCGGCCTGTCCTGCTCGTAAACCAGCCAGACATAGCGGTGGAGGCCTGTGGGGAGAGGCAGAGG AGCGGCCTGTCCTGCTCGTAAACCAGCCAGACGTAGCGGTGGAGGCCTGTGGGGAGAGGCAGAGG T C lnc-TAOK3-9 RNACentral:URS00008C3066 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:118139451..118144975 32194978 MeRIP-seq:(Medium) rs775291216 Functional Loss SNV dbSNP153 33..33 33 - - - 85837 RMVar_ID_85837 Human_SNP_ID_517583669 m1A Human chr12 + 118246206 118246182 118246206 AGTGGCATCCGGGGCCGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGG AGTGGCATC________________________CGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGG CCGGGGCCGGGGTCGCGGCCGTGGA C RPS2P5 Ensembl:ENSG00000240342 Pseudogene exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,H2O2 treatment;HEK293T,untreat control chr12:118246132..118246230;chr12:118246105..118246252 26863410 MeRIP-seq:(Medium) rs1323419613 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_17358397,Human_RBP_ID_17673054,Human_RBP_ID_18926339,Human_RBP_ID_22369890 Human_miRNA_ID_1819910 85838 RMVar_ID_85838 Human_SNP_ID_517583692 m1A Human chr12 + 118246221 118246221 118246221 CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGGGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA A G RPS2P5 Ensembl:ENSG00000240342 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:118246126..118246412 26863410 MeRIP-seq:(Medium) rs1039581962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17673054,Human_RBP_ID_18926339 85839 RMVar_ID_85839 Human_SNP_ID_517583891 m1A Human chr12 + 118246858 118246858 118246858 ACAGCTACCTGACCCCCGACCTCTGGAAGGAGACTGTATTTACCAAGTCTCCCTATCAGGAATTC ACAGCTACCTGACCCCCGACCTCTGGAAGGAGGCTGTATTTACCAAGTCTCCCTATCAGGAATTC A G RPS2P5 Ensembl:ENSG00000240342 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1218570948 Functional Loss SNV dbSNP153 33..33 33 - - - 85840 RMVar_ID_85840 Human_SNP_ID_517583913 m1A Human chr12 + 118246943 118246943 118246943 CCACACCAGAGTCTCCGTGCAGCGGACTCAGGATCCAGCTGTGGCTACAACATAGGGTTTTTATA CCACACCAGAGTCTCCGTGCAGCGGACTCAGGCTCCAGCTGTGGCTACAACATAGGGTTTTTATA A C RPS2P5 Ensembl:ENSG00000240342 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs459229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1822427 85841 RMVar_ID_85841 Human_SNP_ID_517588402 m1A Human chr12 - 118266761 118266761 118266761 GATAATTATGTATTTTGTTCTTCTTTTTCTATAGGTTGCATCATAAATACAAAGGACTGAAGTTA GATAATTATGTATTTTGTTCTTCTTTTTCTATGGGTTGCATCATAAATACAAAGGACTGAAGTTA T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:118266731..118266826;chr12:118266740..118266824 26863196 MeRIP-seq:(Medium) rs750539695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9344379 RMVar_hsa_circ_350697 85842 RMVar_ID_85842 Human_SNP_ID_517612091 m1A Human chr12 + 118371344 118371344 118371344 TTTCATTAAGATCAGGAAGCCCCTCGCTTTCAAGACATCCACATCAGACTCTAAGGAACGAATGC TTTCATTAAGATCAGGAAGCCCCTCGCTTTCAGGACATCCACATCAGACTCTAAGGAACGAATGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:118371340..118371560 32194978 MeRIP-seq:(Medium) rs928366129 Functional Loss SNV dbSNP153 33..33 33 - - - 85843 RMVar_ID_85843 Human_SNP_ID_517613530 m1A Human chr12 + 118376736 118376736 118376736 GGGCTGCTGGCCCCGGCCCCGGCCCAGGCTGGAGCGCCGCCGGCCCCCGAGTACTACCCCGAGGA GGGCTGCTGGCCCCGGCCCCGGCCCAGGCTGGGGCGCCGCCGGCCCCCGAGTACTACCCCGAGGA A G SUDS3 Ensembl:ENSG00000111707 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:118376576..118376775 26863196 MeRIP-seq:(Medium) rs533642265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1431355 85844 RMVar_ID_85844 Human_SNP_ID_517627738 m1A Human chr12 + 118432783 118432783 118432783 GTCTCAAAAAAAAAAAAAGGTGGGGGTGGGGGAGATTGAAAAGAATGGATAATTCTGCCAAAATG GTCTCAAAAAAAAAAAAAGGTGGGGGTGGGGGGGATTGAAAAGAATGGATAATTCTGCCAAAATG A G lnc-SUDS3-1 RNACentral:URS00008B7E0D lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:118432699..118432786 26863410 MeRIP-seq:(Medium) rs1391623458 Functional Loss SNV dbSNP153 33..33 33 - - - 85845 RMVar_ID_85845 Human_SNP_ID_517805656 m1A Human chr12 - 119179384 119179384 119179384 AAGCCATCATCCAGCAGGCGAGAGGAGAGGGGAGAGTCCCGGAAGGGGTCTCGGCGCAGGCGGCT AAGCCATCATCCAGCAGGCGAGAGGAGAGGGGTGAGTCCCGGAAGGGGTCTCGGCGCAGGCGGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:119179334..119179476 26863196 MeRIP-seq:(Medium) rs1450980070 Functional Loss SNV dbSNP153 33..33 33 - - - 85846 RMVar_ID_85846 Human_SNP_ID_517876718 m1A Human chr12 + 119480601 119480599 119480602 TCATCATCACCATCATCCTCATCACCATCATCACCATCACCATCATCATCATCATCACCATCACC TCATCATCACCATCATCCTCATCACCATCAT___CATCACCATCATCATCATCATCACCATCACC TCAC T CCDC60 Ensembl:ENSG00000183273 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:119480518..119480649 26863196 MeRIP-seq:(Medium) rs1354089355 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_36599 85847 RMVar_ID_85847 Human_SNP_ID_517876877 m1A Human chr12 - 119480914 119480914 119480914 TGGTGGTGATGATGATGGTGATGATGATGGTGATGGTGAGGATGGTGGTGATGATGGTGGTGATG TGGTGGTGATGATGATGGTGATGATGATGGTGGTGGTGAGGATGGTGGTGATGATGGTGGTGATG T C AC002070.1 Ensembl:ENSG00000248636 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:119480815..119480960 26863196 MeRIP-seq:(Medium) rs1298873283 Functional Loss SNV dbSNP153 33..33 33 - - - 85848 RMVar_ID_85848 Human_SNP_ID_517925766 m1A Human chr12 - 119688235 119688235 119688235 TTTCACTCCTAGGTCTGGGACCAGTCTTCAGTATAAATCTCAGCCAGAAAAACCAACTCCTCATC TTTCACTCCTAGGTCTGGGACCAGTCTTCAGTGTAAATCTCAGCCAGAAAAACCAACTCCTCATC T C CIT Ensembl:ENSG00000122966 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:119688185..119690231 32194978 MeRIP-seq:(Medium) rs773882555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1431754,Human_Splice_Rec_1431848,Human_Splice_Rec_1431924,Human_Splice_Rec_1432020,Human_Splice_Rec_1432094 85849 RMVar_ID_85849 Human_SNP_ID_517937322 m1A Human chr12 - 119734215 119734215 119734215 GAGCGTCCTGGGTGATGAGAAATCCCAGTTTGAGTGTCGGGTTCGAGAGCTGCAGAGAATGCTGG GAGCGTCCTGGGTGATGAGAAATCCCAGTTTGGGTGTCGGGTTCGAGAGCTGCAGAGAATGCTGG T C CIT Ensembl:ENSG00000122966 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:119734102..119734277 26863196 MeRIP-seq:(Medium) rs748189048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113786,Human_RBP_ID_873905,Human_RBP_ID_8786947,Human_RBP_ID_22040116,Human_RBP_ID_22710109,Human_RBP_ID_26322126,Human_RBP_ID_27806084 Human_Splice_Rec_1431711,Human_Splice_Rec_1431805,Human_Splice_Rec_1431881,Human_Splice_Rec_1431977,Human_Splice_Rec_1432051,Human_Splice_Rec_1432139 RMVar_hsa_circ_101,RMVar_hsa_circ_73319,RMVar_hsa_circ_26394,RMVar_hsa_circ_34030,RMVar_hsa_circ_39016,RMVar_hsa_circ_26447,RMVar_hsa_circ_43973,RMVar_hsa_circ_19885,RMVar_hsa_circ_378973,RMVar_hsa_circ_58916,RMVar_hsa_circ_35344,RMVar_hsa_circ_342044,RMVar_hsa_circ_366785,RMVar_hsa_circ_16497,RMVar_hsa_circ_22067,RMVar_hsa_circ_311051,RMVar_hsa_circ_7120,RMVar_hsa_circ_344956,RMVar_hsa_circ_32815 85850 RMVar_ID_85850 Human_SNP_ID_517965546 m1A Human chr12 + 119856561 119856555 119856561 CTGAACCACTGAACACACACACACACCCACACACACACACTTGCATAGCATTCTAGTACTCCAGA CTGAACCACTGAACACACACACACACC______CACACACTTGCATAGCATTCTAGTACTCCAGA CCACACA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:119856559..119856737 26863196 MeRIP-seq:(Medium) rs765878824 Functional Loss DEL dbSNP153 28..33 33 - - - 85851 RMVar_ID_85851 Human_SNP_ID_517965547 m1A Human chr12 + 119856561 119856555 119856561 CTGAACCACTGAACACACACACACACCCACACACACACACTTGCATAGCATTCTAGTACTCCAGA CTGAACCACTGAACACACACACACACCCACA__CACACACTTGCATAGCATTCTAGTACTCCAGA CCACACA CCACA - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:119856559..119856737 26863196 MeRIP-seq:(Medium) rs765878824 Functional Loss DEL dbSNP153 32..33 33 - - - 85852 RMVar_ID_85852 Human_SNP_ID_713033913 m1A Human chrX - 30215657 30215657 30215657 GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCACCTTGACTGCCGACCAGTCCTGAGAATTCACC GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCTCCTTGACTGCCGACCAGTCCTGAGAATTCACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:30215614..30215712 26863196 MeRIP-seq:(Medium) rs113294066 Functional Loss SNV dbSNP153 33..33 33 - - - 85853 RMVar_ID_85853 Human_SNP_ID_713033914 m1A Human chrX - 30215657 30215657 30215657 GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCACCTTGACTGCCGACCAGTCCTGAGAATTCACC GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCGCCTTGACTGCCGACCAGTCCTGAGAATTCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:30215614..30215712 26863196 MeRIP-seq:(Medium) rs113294066 Functional Loss SNV dbSNP153 33..33 33 - - - 85854 RMVar_ID_85854 Human_SNP_ID_713033915 m1A Human chrX - 30215657 30215657 30215657 GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCACCTTGACTGCCGACCAGTCCTGAGAATTCACC GGTGGTCTCTTCAGTTTACACTCAGGGTCCTCCCCTTGACTGCCGACCAGTCCTGAGAATTCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:30215614..30215712 26863196 MeRIP-seq:(Medium) rs113294066 Functional Loss SNV dbSNP153 33..33 33 - - - 85855 RMVar_ID_85855 Human_SNP_ID_713208756 m1A Human chrX + 31190627 31190613 31190627 GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGAGGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGGGGGGGGGGGGGAG______________GGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGAGGGCGGGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:31190498..31190626 26863196 MeRIP-seq:(Medium) rs1353647821 Functional Loss DEL dbSNP153 20..33 33 - - - 85856 RMVar_ID_85856 Human_SNP_ID_713208761 m1A Human chrX + 31190627 31190620 31190627 GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGAGGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGGGGGGGGGGGGGAGGGGGAGG_______GGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGCGGGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:31190498..31190626 26863196 MeRIP-seq:(Medium) rs1213427749 Functional Loss DEL dbSNP153 27..33 33 - - - 85857 RMVar_ID_85857 Human_SNP_ID_713208764 m1A Human chrX + 31190627 31190625 31190627 GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGAGGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGG__GGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:31190498..31190626 26863196 MeRIP-seq:(Medium) rs1485989921 Functional Loss DEL dbSNP153 32..33 33 - - - 85858 RMVar_ID_85858 Human_SNP_ID_713208765 m1A Human chrX + 31190627 31190626 31190627 GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGAGGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGG_GGGGGTGCTACTAGCATTTAGTAGATAGAGGC GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:31190498..31190626 26863196 MeRIP-seq:(Medium) rs1209519869 Functional Loss DEL dbSNP153 33..33 33 - - - 85859 RMVar_ID_85859 Human_SNP_ID_713208767 m1A Human chrX + 31190627 31190627 31190627 GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGAGGGGGTGCTACTAGCATTTAGTAGATAGAGGC GGGGGGGGGGGGGGGGGAGGGGGAGGGCGGGGGGGGGGTGCTACTAGCATTTAGTAGATAGAGGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:31190498..31190626 26863196 MeRIP-seq:(Medium) rs893367880 Functional Loss SNV dbSNP153 33..33 33 - - - 85860 RMVar_ID_85860 Human_SNP_ID_713223619 m1A Human chrX + 31266886 31266886 31266886 TGTGGGTACGAGTGGAGGAGTGAGCTTCCCAGAGCCGCCGGGCTCCCCGAAAGTGGAGCGCCGCC TGTGGGTACGAGTGGAGGAGTGAGCTTCCCAGCGCCGCCGGGCTCCCCGAAAGTGGAGCGCCGCC A C NONHSAG054214.2 RNACentral:URS00008BD88B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:31266835..31266913 26863196 MeRIP-seq:(Medium) rs747119156 Functional Loss SNV dbSNP153 33..33 33 - - - 85861 RMVar_ID_85861 Human_SNP_ID_714350068 m1A Human chrX + 37480137 37480136 37480138 ACCAGCAGAGAGGAGAGAGACAGAGGAGGGAAAGAGAGAGAGAGGAAAAAGAGAGAGAGAGAGGA ACCAGCAGAGAGGAGAGAGACAGAGGAGGGAA__AGAGAGAGAGGAAAAAGAGAGAGAGAGAGGA AAG A AF241726.2 Ensembl:ENSG00000250349 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:37480087..37480194 26863196 MeRIP-seq:(Medium) rs781893565 Functional Loss DEL dbSNP153 33..34 33 - - - 85862 RMVar_ID_85862 Human_SNP_ID_714350127 m1A Human chrX + 37480248 37480248 37480248 GAGAGAGAGATAGAAGTAGTAAAGAGAAAACAATGTACCATATTCCTTTAAAGCCCAGGGTAAAT GAGAGAGAGATAGAAGTAGTAAAGAGAAAACAGTGTACCATATTCCTTTAAAGCCCAGGGTAAAT A G AF241726.2 Ensembl:ENSG00000250349 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:37480093..37480247 26863196 MeRIP-seq:(Medium) rs1459043740 Functional Loss SNV dbSNP153 33..33 33 - - - 85863 RMVar_ID_85863 Human_SNP_ID_714386172 m1A Human chrX - 37685854 37685854 37685854 GCCCGAGGGGCTCCCAGCATGCCCAGCCCCAAACCGCTCCCGCGCTCTGCGCAGCCCGCCGAGGG GCCCGAGGGGCTCCCAGCATGCCCAGCCCCAACCCGCTCCCGCGCTCTGCGCAGCCCGCCGAGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:37685803..37686017 26863196 MeRIP-seq:(Medium) rs1556439995 Functional Loss SNV dbSNP153 33..33 33 - - - 85864 RMVar_ID_85864 Human_SNP_ID_714386247 m1A Human chrX + 37686071 37686071 37686071 CACCTACCGCTCGGGCGGGGACCGCATGTGGCAGGCGCTGACGTTGCTTTTCTCGCTACTGCCTT CACCTACCGCTCGGGCGGGGACCGCATGTGGCCGGCGCTGACGTTGCTTTTCTCGCTACTGCCTT A C XK,AF241726.2 Ensembl:ENSG00000047597,Ensembl:ENSG00000250349 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:37686024..37686187 26863196 MeRIP-seq:(Medium) rs1187940445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103744,RMVar_hsa_circ_261970 85865 RMVar_ID_85865 Human_SNP_ID_714413733 m1A Human chrX + 37847434 37847434 37847434 CTGGGAGACCACCCGGCAAGAGCCCCGCGCAGAGGAAGGCGGGAGTGGGGGGCGCTCCCAGGTAG CTGGGAGACCACCCGGCAAGAGCCCCGCGCAGGGGAAGGCGGGAGTGGGGGGCGCTCCCAGGTAG A G AF241726.2 Ensembl:ENSG00000250349 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:37847433..37847571 26863196 MeRIP-seq:(Medium) rs772812431 Functional Loss SNV dbSNP153 33..33 33 - - - 85866 RMVar_ID_85866 Human_SNP_ID_714413734 m1A Human chrX + 37847434 37847434 37847434 CTGGGAGACCACCCGGCAAGAGCCCCGCGCAGAGGAAGGCGGGAGTGGGGGGCGCTCCCAGGTAG CTGGGAGACCACCCGGCAAGAGCCCCGCGCAGTGGAAGGCGGGAGTGGGGGGCGCTCCCAGGTAG A T AF241726.2 Ensembl:ENSG00000250349 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:37847433..37847571 26863196 MeRIP-seq:(Medium) rs772812431 Functional Loss SNV dbSNP153 33..33 33 - - - 85867 RMVar_ID_85867 Human_SNP_ID_714436617 m1A Human chrX + 37977327 37977327 37977327 GAAGCCATCCTACTCAGTACTAGGGATGGAAAAAAAACATTTTGTAGACATCAAGGAGAAAGAAG GAAGCCATCCTACTCAGTACTAGGGATGGAAAGAAAACATTTTGTAGACATCAAGGAGAAAGAAG A G AF241726.2 Ensembl:ENSG00000250349 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:37977296..37977491 26863196 MeRIP-seq:(Medium) rs973902423 Functional Loss SNV dbSNP153 33..33 33 - - - 85868 RMVar_ID_85868 Human_SNP_ID_714489125 m1A Human chrX - 38285772 38285770 38285773 AGAGGGGAAGTATCAGGAGACAGGCGAAGAAGAGAATGAAAGGCAGGATGGAGAGGAGTACAAAA AGAGGGGAAGTATCAGGAGACAGGCGAAGAA___AATGAAAGGCAGGATGGAGAGGAGTACAAAA TCTC T RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:38285722..38285943 26863196 MeRIP-seq:(Medium) rs1451816877 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5232106,Human_RBP_ID_8226495,Human_RBP_ID_24340586 RMVar_hsa_circ_47843 85869 RMVar_ID_85869 Human_SNP_ID_714489132 m1A Human chrX - 38285802 38285799 38285802 CAGGAGGAACAGAGAAGAGGAGGAGGAAGAAGAGGGGAAGTATCAGGAGACAGGCGAAGAAGAGA CAGGAGGAACAGAGAAGAGGAGGAGGAAGAAG___GGAAGTATCAGGAGACAGGCGAAGAAGAGA CCCT C RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:38285644..38285979 26863196 MeRIP-seq:(Medium) rs1184900573 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8226495,Human_RBP_ID_24340586 RMVar_hsa_circ_47843 85870 RMVar_ID_85870 Human_SNP_ID_714489145 m1A Human chrX - 38285833 38285833 38285833 AAAGGGAAAAGGAGGGGGAAGGAGAAGAAAACAGGAGGAACAGAGAAGAGGAGGAGGAAGAAGAG AAAGGGAAAAGGAGGGGGAAGGAGAAGAAAACTGGAGGAACAGAGAAGAGGAGGAGGAAGAAGAG T A RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:38285747..38285948 26863196 MeRIP-seq:(Medium) rs141583035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5231127,Human_RBP_ID_8226495 RMVar_hsa_circ_47843 85871 RMVar_ID_85871 Human_SNP_ID_714489155 m1A Human chrX - 38285865 38285863 38285866 AGAGGAAGAGGAAGGAGAGGAGGAAGGAGAAGAAAGGGAAAAGGAGGGGGAAGGAGAAGAAAACA AGAGGAAGAGGAAGGAGAGGAGGAAGGAGAA___AGGGAAAAGGAGGGGGAAGGAGAAGAAAACA TTTC T RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:38285781..38286068 26863196 MeRIP-seq:(Medium) rs781560777 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8226496 RMVar_hsa_circ_47843 85872 RMVar_ID_85872 Human_SNP_ID_714489480 m1A Human chrX - 38286296 38286296 38286296 GGAGAAGGGGAGGGAGAAGAGGAGGAAGGAGAAGGGGAGGGAGAAGAGGAAGGAGAAGGGGAGGG GGAGAAGGGGAGGGAGAAGAGGAGGAAGGAGAGGGGGAGGGAGAAGAGGAAGGAGAAGGGGAGGG T C RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:38286294..38286445 26863196 MeRIP-seq:(Medium) rs1368230530 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_47843 85873 RMVar_ID_85873 Human_SNP_ID_714489723 m1A Human chrX - 38286762 38286761 38286763 TGGAGAAGGAGAAGAAGAGGAGGGAGACAGAGAAGAGGAAGAAGAGAAGGAGGGAGAAGGGAAAG TGGAGAAGGAGAAGAAGAGGAGGGAGACAGA__AGAGGAAGAAGAGAAGGAGGGAGAAGGGAAAG TTC T RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:38286603..38286805 26863196 MeRIP-seq:(Medium) rs1555961852 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8226497 Clinvar_Rec_452 RMVar_hsa_circ_47843 85874 RMVar_ID_85874 Human_SNP_ID_714489737 m1A Human chrX - 38286785 38286785 38286785 GAGGAGGGAGGGGAGGAGGAGCATGGAGAAGGAGAAGAAGAGGAGGGAGACAGAGAAGAGGAAGA GAGGAGGGAGGGGAGGAGGAGCATGGAGAAGGGGAAGAAGAGGAGGGAGACAGAGAAGAGGAAGA T C RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:38286594..38287194 26863196 MeRIP-seq:(Medium) rs748570356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8226497 RMVar_hsa_circ_47843 85875 RMVar_ID_85875 Human_SNP_ID_714489777 m1A Human chrX - 38286937 38286937 38286937 GGGAGAAAGACAAGGGTAGAGGAGAAATGGAGAGGCCAGGAGAGGGAGAGAAGGAACTAGCAGAG GGGAGAAAGACAAGGGTAGAGGAGAAATGGAGTGGCCAGGAGAGGGAGAGAAGGAACTAGCAGAG T A RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:38286900..38287035 26863196 MeRIP-seq:(Medium) rs1427093009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16092,Human_RBP_ID_8226991 RMVar_hsa_circ_47843 85876 RMVar_ID_85876 Human_SNP_ID_714489781 m1A Human chrX - 38286947 38286947 38286947 AGGGAGAAGGGGGAGAAAGACAAGGGTAGAGGAGAAATGGAGAGGCCAGGAGAGGGAGAGAAGGA AGGGAGAAGGGGGAGAAAGACAAGGGTAGAGGGGAAATGGAGAGGCCAGGAGAGGGAGAGAAGGA T C RPGR Ensembl:ENSG00000156313 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:38286544..38286994 26863196 MeRIP-seq:(Medium) rs753818354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070869 RMVar_hsa_circ_47843 85877 RMVar_ID_85877 Human_SNP_ID_714556135 m1A Human chrX + 38688161 38688161 38688161 TGTCCATTTTGTGAAGCCCTGTTGTGCCACAGAGTGTAGCCAGGTCCCCCTGCAGCTAGTCCTAG TGTCCATTTTGTGAAGCCCTGTTGTGCCACAGGGTGTAGCCAGGTCCCCCTGCAGCTAGTCCTAG A G TSPAN7 Ensembl:ENSG00000156298 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:38688111..38688190 26863196 MeRIP-seq:(Medium) rs1216406493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_734329,Human_RBP_ID_5124865,Human_RBP_ID_8226992,Human_RBP_ID_17328232,Human_RBP_ID_18963876 85878 RMVar_ID_85878 Human_SNP_ID_714575799 m1A Human chrX + 38804947 38804947 38804947 CGTCCCTGCGCTCCAACGTCCGCGCGGCCACCATGATGCAAATCTGCGACACCTACAACCAGAAG CGTCCCTGCGCTCCAACGTCCGCGCGGCCACCGTGATGCAAATCTGCGACACCTACAACCAGAAG A G MID1IP1 Ensembl:ENSG00000165175 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:38804901..38804975 26863196 MeRIP-seq:(Medium) rs759263900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5432110,Human_RBP_ID_18919396,Human_RBP_ID_27551549 85879 RMVar_ID_85879 Human_SNP_ID_714575821 m1A Human chrX - 38805055 38805055 38805055 CCCGGGGTCAGCCAGGGGCACGTCGCGCAGCAAGCTGGGCACCATCACCGTCTGGTCCATGTTGT CCCGGGGTCAGCCAGGGGCACGTCGCGCAGCAGGCTGGGCACCATCACCGTCTGGTCCATGTTGT T C NONHSAG054249.2,LOC105373174 RNACentral:URS00009BE43E,RNACentral:URS00009B832B lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:38805005..38805199 26863196 MeRIP-seq:(Medium) rs368433423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261990 85880 RMVar_ID_85880 Human_SNP_ID_714576014 m1A Human chrX - 38805642 38805614 38805642 CTCACACGTGGCCCCCTCCTCCACGCAGCCCCACCGCGCCTCCTGCACGTACGCAGCCCCCCAGT CTCACACGTGGCCCCCTCCTCCACGCAGCCCC____________________________CCAGT GGGGGCTGCGTACGTGCAGGAGGCGCGGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:38805305..38805800;chrX:38805305..38806025;chrX:38805281..38805809 26863196 MeRIP-seq:(Medium) rs1286865023 Functional Loss DEL dbSNP153 33..60 33 - - - 85881 RMVar_ID_85881 Human_SNP_ID_714576022 m1A Human chrX - 38805642 38805642 38805642 CTCACACGTGGCCCCCTCCTCCACGCAGCCCCACCGCGCCTCCTGCACGTACGCAGCCCCCCAGT CTCACACGTGGCCCCCTCCTCCACGCAGCCCCCCCGCGCCTCCTGCACGTACGCAGCCCCCCAGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:38805305..38805800;chrX:38805305..38806025;chrX:38805281..38805809 26863196 MeRIP-seq:(Medium) rs772768826 Functional Loss SNV dbSNP153 33..33 33 - - - 85882 RMVar_ID_85882 Human_SNP_ID_714740753 m1A Human chrX - 39756023 39756023 39756023 TTTGTCAGCCTCCAGAGCTGCAGAAGGACACTATCTTGGGCATGAATATCCCACAGCAGCAGTGC TTTGTCAGCCTCCAGAGCTGCAGAAGGACACTGTCTTGGGCATGAATATCCCACAGCAGCAGTGC T C HSALNG0137369 RNACentral:URS0000EA336D lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:39755974..39756079 26863196 MeRIP-seq:(Medium) rs907386039 Functional Loss SNV dbSNP153 33..33 33 - - - 85883 RMVar_ID_85883 Human_SNP_ID_714787047 m1A Human chrX + 40014121 40014121 40014121 ACAGCGACTGAGAGCGCGCCCTCTCCACCCCCACCCCCGCCGTCGCCGCCTCTCCTGGGGAGCTC ACAGCGACTGAGAGCGCGCCCTCTCCACCCCCCCCCCCGCCGTCGCCGCCTCTCCTGGGGAGCTC A C lnc-ATP6AP2-16 RNACentral:URS0000D5C501 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:40014032..40014180 26863196 MeRIP-seq:(Medium) rs922350103 Functional Loss SNV dbSNP153 33..33 33 - - - 85884 RMVar_ID_85884 Human_SNP_ID_714796447 m1A Human chrX - 40062240 40062240 40062240 CACAGCTGCCATGCTCAAGTTCCCCTCAGGAGACCACCCAGTCTCGCCCTATGCCGCCGGAAGCA CACAGCTGCCATGCTCAAGTTCCCCTCAGGAGGCCACCCAGTCTCGCCCTATGCCGCCGGAAGCA T C BCOR Ensembl:ENSG00000183337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:40062189..40062392 26863196 MeRIP-seq:(Medium) rs759697698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94335,Human_RBP_ID_8935102,Human_RBP_ID_9317827,Human_RBP_ID_9409119,Human_RBP_ID_17326165,Human_RBP_ID_18150480,Human_RBP_ID_26835360 Human_miRNA_ID_3086969 RMVar_hsa_circ_18698,RMVar_hsa_circ_267549,RMVar_hsa_circ_330242,RMVar_hsa_circ_261991 85885 RMVar_ID_85885 Human_SNP_ID_714799124 m1A Human chrX + 40074312 40074312 40074312 CCGAGTAGGTGTCTGCAGCAGGCTGGGTGGGAAGGTGGACTCGGGGTGACGGCCGAGGCGAGGGG CCGAGTAGGTGTCTGCAGCAGGCTGGGTGGGATGGTGGACTCGGGGTGACGGCCGAGGCGAGGGG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:40074221..40074346 26863196 MeRIP-seq:(Medium) rs927300379 Functional Loss SNV dbSNP153 33..33 33 - - - 85886 RMVar_ID_85886 Human_SNP_ID_714799226 m1A Human chrX - 40074599 40074599 40074599 ACCAATGGGGAGCGCTTTCTCTACCTGCCGCCACCTCACTACGTCGGTCCCCACATCCCATCGTC ACCAATGGGGAGCGCTTTCTCTACCTGCCGCCCCCTCACTACGTCGGTCCCCACATCCCATCGTC T G BCOR Ensembl:ENSG00000183337 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:40074550..40074642 26863196 MeRIP-seq:(Medium) rs1206495071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1062413,Human_RBP_ID_3976367,Human_RBP_ID_5535598,Human_RBP_ID_9317280,Human_RBP_ID_17326193,Human_RBP_ID_17441408,Human_RBP_ID_17554344,Human_RBP_ID_18150518,Human_RBP_ID_18197271,Human_RBP_ID_18454316,Human_RBP_ID_22841305,Human_RBP_ID_26834636,Human_RBP_ID_27381607,Human_RBP_ID_27551652 RMVar_hsa_circ_267549,RMVar_hsa_circ_22908,RMVar_hsa_circ_365533 85887 RMVar_ID_85887 Human_SNP_ID_714803487 m1A Human chrX + 40096149 40096149 40096149 CGCCTTGGCCGAGGATCTTGCCCCGGTGCGCAAGTTCCTCTTCGCCTACAGCCTCCTTGCCACAC CGCCTTGGCCGAGGATCTTGCCCCGGTGCGCAGGTTCCTCTTCGCCTACAGCCTCCTTGCCACAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:40096147..40096247 26863196 MeRIP-seq:(Medium) rs1368652277 Functional Loss SNV dbSNP153 33..33 33 - - - 85888 RMVar_ID_85888 Human_SNP_ID_714803946 m1A Human chrX - 40097815 40097815 40097815 GAGAGCGGGAGCTAGGCGGGCGGCGGCGGCGGAGGGGGAGCCCGCGAGCCGCCGGGCGGAGAGCC GAGAGCGGGAGCTAGGCGGGCGGCGGCGGCGGGGGGGGAGCCCGCGAGCCGCCGGGCGGAGAGCC T C BCOR Ensembl:ENSG00000183337 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:40097726..40097950 26863410 MeRIP-seq:(Medium) rs1000594582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258161,Human_RBP_ID_5075775,Human_RBP_ID_8226516,Human_RBP_ID_9339916,Human_RBP_ID_22468265,Human_RBP_ID_22734246,Human_RBP_ID_26797271 85889 RMVar_ID_85889 Human_SNP_ID_714891791 m1A Human chrX - 40581071 40581071 40581071 CCCGCCACCAACGCCAGGAGCACGACAAACACAGCCATGGTGCCGCGGCGGCCGCAGCACTGCGG CCCGCCACCAACGCCAGGAGCACGACAAACACGGCCATGGTGCCGCGGCGGCCGCAGCACTGCGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:40581051..40581075 26863196 MeRIP-seq:(Medium) rs11553342 Functional Loss SNV dbSNP153 33..33 33 - - - 85890 RMVar_ID_85890 Human_SNP_ID_714918322 m1A Human chrX - 40735344 40735344 40735344 CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGACCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGGCCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG T C MED14 Ensembl:ENSG00000180182 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:40735252..40735346 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9317851 85891 RMVar_ID_85891 Human_SNP_ID_714918323 m1A Human chrX - 40735344 40735344 40735344 CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGACCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGCCCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG T G MED14 Ensembl:ENSG00000180182 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:40735252..40735346 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9317851 85892 RMVar_ID_85892 Human_SNP_ID_714979313 m1A Human chrX - 41085750 41085749 41085750 CGTCACCTCCTCCTGCTCCTCCTCCTGCAGCGACGGCTTCACCTTCCCCTAGTCGCCGCCTCTGT CGTCACCTCCTCCTGCTCCTCCTCCTGCAGCG_CGGCTTCACCTTCCCCTAGTCGCCGCCTCTGT GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:41085626..41086051;chrX:41085616..41085984;chrX:41085576..41086051 26863196 MeRIP-seq:(Medium) rs1194047128 Functional Loss DEL dbSNP153 33..33 33 - - - 85893 RMVar_ID_85893 Human_SNP_ID_714979314 m1A Human chrX - 41085750 41085750 41085750 CGTCACCTCCTCCTGCTCCTCCTCCTGCAGCGACGGCTTCACCTTCCCCTAGTCGCCGCCTCTGT CGTCACCTCCTCCTGCTCCTCCTCCTGCAGCGCCGGCTTCACCTTCCCCTAGTCGCCGCCTCTGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:41085626..41086051;chrX:41085616..41085984;chrX:41085576..41086051 26863196 MeRIP-seq:(Medium) rs1247653527 Functional Loss SNV dbSNP153 33..33 33 - - - 85894 RMVar_ID_85894 Human_SNP_ID_714979324 m1A Human chrX + 41085795 41085795 41085795 AGGAGCAGGAGGAGGTGACGCAGGAGAAACGCACCGCCCGGAGCCCGTCTGAGCTCAGCGAGAGC AGGAGCAGGAGGAGGTGACGCAGGAGAAACGCTCCGCCCGGAGCCCGTCTGAGCTCAGCGAGAGC A T USP9X Ensembl:ENSG00000124486 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:41085776..41085800 26863196 MeRIP-seq:(Medium) rs1026669782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257309,Human_RBP_ID_968033,Human_RBP_ID_3977156,Human_RBP_ID_5075783,Human_RBP_ID_5535600,Human_RBP_ID_8938607,Human_RBP_ID_9317285,Human_RBP_ID_18919546,Human_RBP_ID_19026533 Human_miRNA_ID_2710275 RMVar_hsa_circ_262025,RMVar_hsa_circ_79754 85895 RMVar_ID_85895 Human_SNP_ID_715026615 m1A Human chrX + 41333747 41333747 41333747 AAAAAAACAAAAACAAAAAAAACGAAAAACGAAAGCTGAGTGCATAGAGTTGGAAAGGGGAGCGA AAAAAAACAAAAACAAAAAAAACGAAAAACGAGAGCTGAGTGCATAGAGTTGGAAAGGGGAGCGA A G DDX3X Ensembl:ENSG00000215301 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:41333649..41333774 26863410 MeRIP-seq:(Medium) rs1489264014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24341452 Human_Splice_Rec_2197482 RMVar_hsa_circ_262124,RMVar_hsa_circ_81835 85896 RMVar_ID_85896 Human_SNP_ID_715026793 m1A Human chrX + 41334226 41334226 41334226 CGGTGGAACAAACACTCGCTTAGCAGCGGAAGACTCCGAGTTCTCGGTACTCTTCAGGGATGAGT CGGTGGAACAAACACTCGCTTAGCAGCGGAAGCCTCCGAGTTCTCGGTACTCTTCAGGGATGAGT A C DDX3X Ensembl:ENSG00000215301 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:41334176..41334346 26863196 MeRIP-seq:(Medium) rs369180129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1714861,Human_RBP_ID_2074384,Human_RBP_ID_3922371,Human_RBP_ID_5076088,Human_RBP_ID_8001766,Human_RBP_ID_8939100,Human_RBP_ID_16887046,Human_RBP_ID_19027206,Human_RBP_ID_23107590 Human_Splice_Rec_2197450,Human_Splice_Rec_2197489,Human_Splice_Rec_2197521,Human_Splice_Rec_2197557,Human_Splice_Rec_2197591,Human_Splice_Rec_2197626,Human_Splice_Rec_2197660,Human_Splice_Rec_2197694,Human_Splice_Rec_2197731,Human_Splice_Rec_2197766,Human_Splice_Rec_2197796,Human_Splice_Rec_2197800,Human_Splice_Rec_2197802,Human_Splice_Rec_2197804,Human_Splice_Rec_2197814,Human_Splice_Rec_2197830,Human_Splice_Rec_2197856,Human_Splice_Rec_2197886,Human_Splice_Rec_2197918,Human_Splice_Rec_2197950,Human_Splice_Rec_2197980,Human_Splice_Rec_2198007,Human_Splice_Rec_2198039,Human_Splice_Rec_2198069,Human_Splice_Rec_2198099,Human_Splice_Rec_2198131,Human_Splice_Rec_2198159,Human_Splice_Rec_2198189,Human_Splice_Rec_2198219,Human_Splice_Rec_2198250,Human_Splice_Rec_2198279,Human_Splice_Rec_2198309,Human_Splice_Rec_2198341,Human_Splice_Rec_2198373,Human_Splice_Rec_2198403,Human_Splice_Rec_2198437,Human_Splice_Rec_2198469,Human_Splice_Rec_2198477 Human_miRNA_ID_2073370,Human_miRNA_ID_2075053,Human_miRNA_ID_2150241,Human_miRNA_ID_3065213 RMVar_hsa_circ_262124,RMVar_hsa_circ_81835 85897 RMVar_ID_85897 Human_SNP_ID_715028735 m1A Human chrX + 41341551 41341551 41341551 AGCAAAGATAAGGATGCGTATAGCAGTTTTGGATCTCGTAGTGATTCAAGAGGGAAGTCTAGCTT AGCAAAGATAAGGATGCGTATAGCAGTTTTGGGTCTCGTAGTGATTCAAGAGGGAAGTCTAGCTT A G DDX3X Ensembl:ENSG00000215301 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:41341501..41341655 26863196 MeRIP-seq:(Medium) rs1401119888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95152,Human_RBP_ID_287796,Human_RBP_ID_734736,Human_RBP_ID_2074428,Human_RBP_ID_5063322,Human_RBP_ID_8001959,Human_RBP_ID_8718724,Human_RBP_ID_8935457,Human_RBP_ID_10462937,Human_RBP_ID_16887468,Human_RBP_ID_18919769,Human_RBP_ID_22519514,Human_RBP_ID_24341484,Human_RBP_ID_27147900 Human_Splice_Rec_2197455,Human_Splice_Rec_2197456,Human_Splice_Rec_2197487,Human_Splice_Rec_2197494,Human_Splice_Rec_2197495,Human_Splice_Rec_2197526,Human_Splice_Rec_2197527,Human_Splice_Rec_2197562,Human_Splice_Rec_2197563,Human_Splice_Rec_2197596,Human_Splice_Rec_2197597,Human_Splice_Rec_2197631,Human_Splice_Rec_2197632,Human_Splice_Rec_2197665,Human_Splice_Rec_2197666,Human_Splice_Rec_2197699,Human_Splice_Rec_2197700,Human_Splice_Rec_2197730,Human_Splice_Rec_2197736,Human_Splice_Rec_2197737,Human_Splice_Rec_2197769,Human_Splice_Rec_2197770,Human_Splice_Rec_2197803,Human_Splice_Rec_2197809,Human_Splice_Rec_2197810,Human_Splice_Rec_2197817,Human_Splice_Rec_2197818,Human_Splice_Rec_2197835,Human_Splice_Rec_2197836,Human_Splice_Rec_2197861,Human_Splice_Rec_2197862,Human_Splice_Rec_2197891,Human_Splice_Rec_2197892,Human_Splice_Rec_2197923,Human_Splice_Rec_2197924,Human_Splice_Rec_2197953,Human_Splice_Rec_2197954,Human_Splice_Rec_2197985,Human_Splice_Rec_2198012,Human_Splice_Rec_2198013,Human_Splice_Rec_2198044,Human_Splice_Rec_2198045,Human_Splice_Rec_2198074,Human_Splice_Rec_2198075,Human_Splice_Rec_2198104,Human_Splice_Rec_2198105,Human_Splice_Rec_2198136,Human_Splice_Rec_2198164,Human_Splice_Rec_2198165,Human_Splice_Rec_2198194,Human_Splice_Rec_2198195,Human_Splice_Rec_2198224,Human_Splice_Rec_2198225,Human_Splice_Rec_2198255,Human_Splice_Rec_2198284,Human_Splice_Rec_2198285,Human_Splice_Rec_2198314,Human_Splice_Rec_2198315,Human_Splice_Rec_2198346,Human_Splice_Rec_2198347,Human_Splice_Rec_2198378,Human_Splice_Rec_2198379,Human_Splice_Rec_2198410,Human_Splice_Rec_2198411,Human_Splice_Rec_2198442,Human_Splice_Rec_2198443,Human_Splice_Rec_2198476,Human_Splice_Rec_2198478,Human_Splice_Rec_2198479,Human_Splice_Rec_2198488,Human_Splice_Rec_2198489,Human_Splice_Rec_2198514,Human_Splice_Rec_2198515,Human_Splice_Rec_2198548,Human_Splice_Rec_2198549,Human_Splice_Rec_2198558,Human_Splice_Rec_2198559,Human_Splice_Rec_2198590,Human_Splice_Rec_2198591,Human_Splice_Rec_2198622,Human_Splice_Rec_2198623,Human_Splice_Rec_2198632,Human_Splice_Rec_2198633,Human_Splice_Rec_2198666,Human_Splice_Rec_2198667,Human_Splice_Rec_2198698,Human_Splice_Rec_2198699,Human_Splice_Rec_2198725,Human_Splice_Rec_2198743,Human_Splice_Rec_2198789,Human_Splice_Rec_2198855,Human_Splice_Rec_2198905 RMVar_hsa_circ_49732,RMVar_hsa_circ_16985,RMVar_hsa_circ_61066,RMVar_hsa_circ_267328,RMVar_hsa_circ_57106 85898 RMVar_ID_85898 Human_SNP_ID_715028952 m1A Human chrX - 41342460 41342460 41342460 GAACAGCACAAGCAATTAATCAGAATCATATCATTTAACCATTATCAGATTCTTATCCCTACTCT GAACAGCACAAGCAATTAATCAGAATCATATCCTTTAACCATTATCAGATTCTTATCCCTACTCT T G RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:41342457..41342593 26863196 MeRIP-seq:(Medium) rs750257027 Functional Loss SNV dbSNP153 33..33 33 - - - 85899 RMVar_ID_85899 Human_SNP_ID_715029136 m1A Human chrX + 41343287 41343287 41343287 ATTGAGCTTACTCGTTATACTCGCCCAACTCCAGTGCAAAAGCATGCTATTCCTATTATCAAAGA ATTGAGCTTACTCGTTATACTCGCCCAACTCCGGTGCAAAAGCATGCTATTCCTATTATCAAAGA A G DDX3X Ensembl:ENSG00000215301 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:41343240..41344243 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_94575,Human_RBP_ID_734738,Human_RBP_ID_1714934,Human_RBP_ID_2074450,Human_RBP_ID_3922406,Human_RBP_ID_5063336,Human_RBP_ID_8001975,Human_RBP_ID_8718735,Human_RBP_ID_8935461,Human_RBP_ID_9265253,Human_RBP_ID_9316709,Human_RBP_ID_16887553,Human_RBP_ID_18919789,Human_RBP_ID_26305462,Human_RBP_ID_27147913 Human_Splice_Rec_2197461,Human_Splice_Rec_2197462,Human_Splice_Rec_2197500,Human_Splice_Rec_2197501,Human_Splice_Rec_2197532,Human_Splice_Rec_2197533,Human_Splice_Rec_2197568,Human_Splice_Rec_2197569,Human_Splice_Rec_2197601,Human_Splice_Rec_2197602,Human_Splice_Rec_2197637,Human_Splice_Rec_2197638,Human_Splice_Rec_2197671,Human_Splice_Rec_2197672,Human_Splice_Rec_2197705,Human_Splice_Rec_2197706,Human_Splice_Rec_2197742,Human_Splice_Rec_2197743,Human_Splice_Rec_2197775,Human_Splice_Rec_2197776,Human_Splice_Rec_2197823,Human_Splice_Rec_2197824,Human_Splice_Rec_2197867,Human_Splice_Rec_2197868,Human_Splice_Rec_2197897,Human_Splice_Rec_2197898,Human_Splice_Rec_2197929,Human_Splice_Rec_2197930,Human_Splice_Rec_2197959,Human_Splice_Rec_2197960,Human_Splice_Rec_2198018,Human_Splice_Rec_2198019,Human_Splice_Rec_2198048,Human_Splice_Rec_2198049,Human_Splice_Rec_2198080,Human_Splice_Rec_2198081,Human_Splice_Rec_2198110,Human_Splice_Rec_2198111,Human_Splice_Rec_2198140,Human_Splice_Rec_2198141,Human_Splice_Rec_2198170,Human_Splice_Rec_2198171,Human_Splice_Rec_2198198,Human_Splice_Rec_2198199,Human_Splice_Rec_2198230,Human_Splice_Rec_2198231,Human_Splice_Rec_2198259,Human_Splice_Rec_2198260,Human_Splice_Rec_2198290,Human_Splice_Rec_2198291,Human_Splice_Rec_2198320,Human_Splice_Rec_2198321,Human_Splice_Rec_2198352,Human_Splice_Rec_2198353,Human_Splice_Rec_2198416,Human_Splice_Rec_2198417,Human_Splice_Rec_2198448,Human_Splice_Rec_2198449,Human_Splice_Rec_2198482,Human_Splice_Rec_2198494,Human_Splice_Rec_2198495,Human_Splice_Rec_2198520,Human_Splice_Rec_2198521,Human_Splice_Rec_2198564,Human_Splice_Rec_2198565,Human_Splice_Rec_2198596,Human_Splice_Rec_2198597,Human_Splice_Rec_2198638,Human_Splice_Rec_2198639,Human_Splice_Rec_2198672,Human_Splice_Rec_2198673,Human_Splice_Rec_2198704,Human_Splice_Rec_2198705,Human_Splice_Rec_2198748,Human_Splice_Rec_2198749,Human_Splice_Rec_2198768,Human_Splice_Rec_2198769,Human_Splice_Rec_2198794,Human_Splice_Rec_2198795,Human_Splice_Rec_2198818,Human_Splice_Rec_2198819,Human_Splice_Rec_2198840,Human_Splice_Rec_2198860,Human_Splice_Rec_2198861,Human_Splice_Rec_2198884,Human_Splice_Rec_2198885,Human_Splice_Rec_2198910,Human_Splice_Rec_2198911,Human_Splice_Rec_2198929,Human_Splice_Rec_2198951,Human_Splice_Rec_2198955 Human_miRNA_ID_2360471 RMVar_hsa_circ_16985,RMVar_hsa_circ_57106,RMVar_hsa_circ_124117,RMVar_hsa_circ_121232,RMVar_hsa_circ_262126,RMVar_hsa_circ_299878,RMVar_hsa_circ_370995,RMVar_hsa_circ_262129,RMVar_hsa_circ_77181,RMVar_hsa_circ_262130,RMVar_hsa_circ_262128 85900 RMVar_ID_85900 Human_SNP_ID_715030007 m1A Human chrX - 41346573 41346573 41346573 CCCGTACGACCAATACGATGTACATATTCTTCAATATCACTTGGCAAGTCAAAATTGATAACATG CCCGTACGACCAATACGATGTACATATTCTTCTATATCACTTGGCAAGTCAAAATTGATAACATG T A RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:41346329..41346574 32194978 MeRIP-seq:(Medium) rs1366730237 Functional Loss SNV dbSNP153 33..33 33 - - - 85901 RMVar_ID_85901 Human_SNP_ID_715030008 m1A Human chrX - 41346573 41346573 41346573 CCCGTACGACCAATACGATGTACATATTCTTCAATATCACTTGGCAAGTCAAAATTGATAACATG CCCGTACGACCAATACGATGTACATATTCTTCGATATCACTTGGCAAGTCAAAATTGATAACATG T C RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:41346329..41346574 32194978 MeRIP-seq:(Medium) rs1366730237 Functional Loss SNV dbSNP153 33..33 33 - - - 85902 RMVar_ID_85902 Human_SNP_ID_715030107 m1A Human chrX - 41346998 41346998 41346998 ATACTATTTATACCTCACCTCTTAGAACGTCCACGACTGCTACCCTTGTAGTGGTGTTCATAAGC ATACTATTTATACCTCACCTCTTAGAACGTCCGCGACTGCTACCCTTGTAGTGGTGTTCATAAGC T C RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:41346876..41347100 26863196 MeRIP-seq:(Medium) rs1420275893 Functional Loss SNV dbSNP153 33..33 33 - - - 85903 RMVar_ID_85903 Human_SNP_ID_715030110 m1A Human chrX - 41347007 41347007 41347007 CCTCATTATATACTATTTATACCTCACCTCTTAGAACGTCCACGACTGCTACCCTTGTAGTGGTG CCTCATTATATACTATTTATACCTCACCTCTTCGAACGTCCACGACTGCTACCCTTGTAGTGGTG T G RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:41346922..41347047;chrX:41346851..41347032 26863196 MeRIP-seq:(Medium) rs1376305594 Functional Loss SNV dbSNP153 33..33 33 - - - 85904 RMVar_ID_85904 Human_SNP_ID_715030276 m1A Human chrX - 41347629 41347628 41347630 TTGTAAAAGCCTCCATAGCCACCTAATGAGAGATTTAAAAAGAGAGAGAAATTAATGAAGTTATC TTGTAAAAGCCTCCATAGCCACCTAATGAGA__TTTAAAAAGAGAGAGAAATTAATGAAGTTATC ATC A RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:41347626..41347750 32194978 MeRIP-seq:(Medium) rs982471233 Functional Loss DEL dbSNP153 32..33 33 - - - 85905 RMVar_ID_85905 Human_SNP_ID_715112217 m1A Human chrX - 41823132 41823132 41823132 GTGGGAGGCAGAGCCACCTGCTGAGAGTAGGCATGGTGGTAGAGAGTAGAGAGATAAGAGAGTTA GTGGGAGGCAGAGCCACCTGCTGAGAGTAGGCGTGGTGGTAGAGAGTAGAGAGATAAGAGAGTTA T C CASK Ensembl:ENSG00000147044 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:41823131..41823245 26863196 MeRIP-seq:(Medium) rs776917139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262161,RMVar_hsa_circ_372506,RMVar_hsa_circ_74132 85906 RMVar_ID_85906 Human_SNP_ID_715127921 m1A Human chrX - 41923519 41923517 41923520 CCCGGGCGGGCGGTGGCGGCTGCGGGAGGAGGAGAAAGAGGAGGGAGCGTCTCTGCCGCCGCCTC CCCGGGCGGGCGGTGGCGGCTGCGGGAGGAG___AAAGAGGAGGGAGCGTCTCTGCCGCCGCCTC TCTC T CASK Ensembl:ENSG00000147044 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:41923328..41923550 26863196 MeRIP-seq:(Medium) rs771661033 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5063644 85907 RMVar_ID_85907 Human_SNP_ID_715450203 m1A Human chrX + 43843761 43843761 43843761 GTCCAGAGTCATGCAGAAGTTTGGCTGCTGCCATACCTGGGAGAAAAGACAGTAAGACATCAGGA GTCCAGAGTCATGCAGAAGTTTGGCTGCTGCCGTACCTGGGAGAAAAGACAGTAAGACATCAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:43843734..43843812 26863196 MeRIP-seq:(Medium) rs1332503515 Functional Loss SNV dbSNP153 33..33 33 - - - 85908 RMVar_ID_85908 Human_SNP_ID_715483458 m1A Human chrX + 44029473 44029473 44029473 AAAAGCAAGAGCAGAAGTCGTAGTCGTGAACGAAAGAGAAGCAAAAGTAAGGAACGGAAGCAAAG AAAAGCAAGAGCAGAAGTCGTAGTCGTGAACGGAAGAGAAGCAAAAGTAAGGAACGGAAGCAAAG A G AL034370.1 Ensembl:ENSG00000214019 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:44029461..44029526 26863196 MeRIP-seq:(Medium) rs995732174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1912450 85909 RMVar_ID_85909 Human_SNP_ID_715524595 m1A Human chrX + 44282664 44282664 44282664 GGGGGTGGGGGGGGGTGGGGGGGTGGGAGAGGAGGACAAAGAAAAAAACAAAAACAAAAAAAAAA GGGGGTGGGGGGGGGTGGGGGGGTGGGAGAGGGGGACAAAGAAAAAAACAAAAACAAAAAAAAAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chrX:44282601..44282675;chrX:44282525..44282675 26863196 MeRIP-seq:(Medium) rs1485755078 Functional Loss SNV dbSNP153 33..33 33 - - - 85910 RMVar_ID_85910 Human_SNP_ID_715570064 m1A Human chrX + 44542717 44542717 44542717 CCTTAAAAAAAAAATGGAGCTCGAAGAATCCTAGGGCAGGGGAAGGAAGAGGTGCCATAGGAGCA CCTTAAAAAAAAAATGGAGCTCGAAGAATCCTCGGGCAGGGGAAGGAAGAGGTGCCATAGGAGCA A C RF00017-1264 RNACentral:URS00009A773B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:44542714..44542982 26863196 MeRIP-seq:(Medium) rs780522836 Functional Loss SNV dbSNP153 33..33 33 - - - 85911 RMVar_ID_85911 Human_SNP_ID_715633805 m1A Human chrX - 44873280 44873272 44873281 CGGGGTTGGGCAGGGGGCAGCCACAGGCGGGGACGGCGGGAACGGCCGGAGCGCGCGGGGCTGGG CGGGGTTGGGCAGGGGGCAGCCACAGGCGGG_________AACGGCCGGAGCGCGCGGGGCTGGG TCCCGCCGTC T RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:44873213..44873340 26863196 MeRIP-seq:(Medium) rs937573583 Functional Loss DEL dbSNP153 32..40 33 - - - 85912 RMVar_ID_85912 Human_SNP_ID_715641209 m1A Human chrX + 44911333 44911333 44911333 CTTCTCAGACGGGGCGGCTGCCGGGCGGAGGGACTCCTCACTTCTCAGACGGGGTGGCCGGGCAG CTTCTCAGACGGGGCGGCTGCCGGGCGGAGGGCCTCCTCACTTCTCAGACGGGGTGGCCGGGCAG A C KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:44911322..44911408 26863196 MeRIP-seq:(Medium) rs1305471768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35166 85913 RMVar_ID_85913 Human_SNP_ID_715641210 m1A Human chrX + 44911333 44911333 44911333 CTTCTCAGACGGGGCGGCTGCCGGGCGGAGGGACTCCTCACTTCTCAGACGGGGTGGCCGGGCAG CTTCTCAGACGGGGCGGCTGCCGGGCGGAGGGGCTCCTCACTTCTCAGACGGGGTGGCCGGGCAG A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:44911322..44911408 26863196 MeRIP-seq:(Medium) rs1305471768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35166 85914 RMVar_ID_85914 Human_SNP_ID_715649101 m1A Human chrX + 44954742 44954742 44954742 ACTCACTGTTATAGGCAGTAGGAAATAATTGGAAGTTTAAGAGCTGGGAAGCATGACAATAAATA ACTCACTGTTATAGGCAGTAGGAAATAATTGGGAGTTTAAGAGCTGGGAAGCATGACAATAAATA A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:44954733..44954835 26863196 MeRIP-seq:(Medium) rs955766922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35166 85915 RMVar_ID_85915 Human_SNP_ID_715657573 m1A Human chrX + 44999529 44999529 44999529 TCAAAATGAGTCAGGGTAGAGTAGGTGATTGAATAAGGGTGGAGCAGGTAATTGAAAAAGGTTGC TCAAAATGAGTCAGGGTAGAGTAGGTGATTGAGTAAGGGTGGAGCAGGTAATTGAAAAAGGTTGC A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:44999312..44999572 26863196 MeRIP-seq:(Medium) rs1317914236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56424,RMVar_hsa_circ_35166,RMVar_hsa_circ_344285,RMVar_hsa_circ_289585,RMVar_hsa_circ_262177,RMVar_hsa_circ_262176,RMVar_hsa_circ_293030 85916 RMVar_ID_85916 Human_SNP_ID_732531034 m1A Human chrX - 135021734 135021734 135021734 CCCCCTCCTCCTCACCAGACTTCCAGACGACTACATCATGCTGCCCACAGACCTGCGCTGCCACT CCCCCTCCTCCTCACCAGACTTCCAGACGACTGCATCATGCTGCCCACAGACCTGCGCTGCCACT T C RTL8B Ensembl:ENSG00000212747 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:135021683..135021905 26863196 MeRIP-seq:(Medium) rs1414367396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5053315,Human_RBP_ID_27549852 85917 RMVar_ID_85917 Human_SNP_ID_732531136 m1A Human chrX + 135021995 135021995 135021995 ACTACGCGGGAGGGGACAGGAGCGCAGGGGACATCGTGGCGGCTCGAGGGGGAGGGAGGCGCGGA ACTACGCGGGAGGGGACAGGAGCGCAGGGGACGTCGTGGCGGCTCGAGGGGGAGGGAGGCGCGGA A G NONHSAG055369.2 RNACentral:URS00008C1347 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:135021984..135022087 26863196 MeRIP-seq:(Medium) rs765829206 Functional Loss SNV dbSNP153 33..33 33 - - - 85918 RMVar_ID_85918 Human_SNP_ID_732531137 m1A Human chrX + 135021995 135021995 135021995 ACTACGCGGGAGGGGACAGGAGCGCAGGGGACATCGTGGCGGCTCGAGGGGGAGGGAGGCGCGGA ACTACGCGGGAGGGGACAGGAGCGCAGGGGACTTCGTGGCGGCTCGAGGGGGAGGGAGGCGCGGA A T NONHSAG055369.2 RNACentral:URS00008C1347 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:135021984..135022087 26863196 MeRIP-seq:(Medium) rs765829206 Functional Loss SNV dbSNP153 33..33 33 - - - 85919 RMVar_ID_85919 Human_SNP_ID_732531322 m1A Human chrX - 135022479 135022479 135022479 CCGGCGAAGCCCAGCGCAGCTCAGCTAAACTCAGCGGAGCCAGCGCGGCGCGATGGAAGGTCGAG CCGGCGAAGCCCAGCGCAGCTCAGCTAAACTCGGCGGAGCCAGCGCGGCGCGATGGAAGGTCGAG T C RTL8B Ensembl:ENSG00000212747 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:135022326..135022550 26863196 MeRIP-seq:(Medium) rs1257786918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5053334 85920 RMVar_ID_85920 Human_SNP_ID_732532945 m1A Human chrX + 135032384 135032384 135032384 CCCATTGACGTCCAGCGAAGCGAGGAGCAGCGATGGACGGTCGGGTGCAGCTGATAAAGGCCCTC CCCATTGACGTCCAGCGAAGCGAGGAGCAGCGGTGGACGGTCGGGTGCAGCTGATAAAGGCCCTC A G RTL8C Ensembl:ENSG00000134590 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:135032351..135032525 26863196 MeRIP-seq:(Medium) rs757859781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258030,Human_RBP_ID_1341215,Human_RBP_ID_1711398,Human_RBP_ID_5076315,Human_RBP_ID_16828167,Human_RBP_ID_24330507 85921 RMVar_ID_85921 Human_SNP_ID_732533043 m1A Human chrX - 135032824 135032821 135032825 CAGGGGACATCGCGGCGGCTCGAGGGGGAGGGAGGCGCGGAGGGAGGGCGCCGGTGGCGACCCTG CAGGGGACATCGCGGCGGCTCGAGGGGGAGG____CGCGGAGGGAGGGCGCCGGTGGCGACCCTG GCCTC G lnc-RTL8B-1,lnc-RTL8B-1:2,lnc-RTL8B-1:3 RNACentral:URS00009BFDA6,RNACentral:URS00008BB198,RNACentral:URS00008C2490 lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:135032801..135032825 26863196 MeRIP-seq:(Medium) rs745600250 Functional Loss DEL dbSNP153 32..35 33 - - - 85922 RMVar_ID_85922 Human_SNP_ID_732533083 m1A Human chrX - 135033002 135033002 135033002 CAGGAGCCCAGCTTGCAGCTGGAGCGCAGGACAGCGTCCAAATGTACATGGGAGGGGCTGGCTGG CAGGAGCCCAGCTTGCAGCTGGAGCGCAGGACTGCGTCCAAATGTACATGGGAGGGGCTGGCTGG T A lnc-RTL8B-1,lnc-RTL8B-1:2,lnc-RTL8B-1:3 RNACentral:URS00009BFDA6,RNACentral:URS00008BB198,RNACentral:URS00008C2490 lincRNA,lincRNA,lincRNA exon,exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:135032951..135033075 32194978 MeRIP-seq:(Medium) rs1327249259 Functional Loss SNV dbSNP153 33..33 33 - - - 85923 RMVar_ID_85923 Human_SNP_ID_732533084 m1A Human chrX - 135033007 135033007 135033007 TGTAACAGGAGCCCAGCTTGCAGCTGGAGCGCAGGACAGCGTCCAAATGTACATGGGAGGGGCTG TGTAACAGGAGCCCAGCTTGCAGCTGGAGCGCCGGACAGCGTCCAAATGTACATGGGAGGGGCTG T G lnc-RTL8B-1,lnc-RTL8B-1:2,lnc-RTL8B-1:3 RNACentral:URS00009BFDA6,RNACentral:URS00008BB198,RNACentral:URS00008C2490 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:135032958..135033100 26863196 MeRIP-seq:(Medium) rs1485505953 Functional Loss SNV dbSNP153 33..33 33 - - - 85924 RMVar_ID_85924 Human_SNP_ID_732533103 m1A Human chrX + 135033149 135033149 135033149 GCCCACAGACCTGCGCTGCCACAGCCATCGCCATCCATCGCATCCCACCGACAGACTGCTGCTCC GCCCACAGACCTGCGCTGCCACAGCCATCGCCGTCCATCGCATCCCACCGACAGACTGCTGCTCC A G RTL8C Ensembl:ENSG00000134590 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:135032852..135033300 26863196 MeRIP-seq:(Medium) rs1453699816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258034,Human_RBP_ID_729054,Human_RBP_ID_17325110,Human_RBP_ID_17440366,Human_RBP_ID_17552987,Human_RBP_ID_22345008 Human_Splice_Rec_2237548 85925 RMVar_ID_85925 Human_SNP_ID_732535885 m1A Human chrX - 135051967 135051967 135051967 CCGACCGACTCCCGGAGTTCATCGTGCAGACGAGCTCCTACATGTTCGTGGACGAGAACACGTTC CCGACCGACTCCCGGAGTTCATCGTGCAGACGTGCTCCTACATGTTCGTGGACGAGAACACGTTC T A RTL8A Ensembl:ENSG00000203950 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2498776 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_2237551,Human_Splice_Rec_2237553,Human_Splice_Rec_2237555 85926 RMVar_ID_85926 Human_SNP_ID_732535886 m1A Human chrX - 135051967 135051967 135051967 CCGACCGACTCCCGGAGTTCATCGTGCAGACGAGCTCCTACATGTTCGTGGACGAGAACACGTTC CCGACCGACTCCCGGAGTTCATCGTGCAGACGGGCTCCTACATGTTCGTGGACGAGAACACGTTC T C RTL8A Ensembl:ENSG00000203950 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2498776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2237551,Human_Splice_Rec_2237553,Human_Splice_Rec_2237555 85927 RMVar_ID_85927 Human_SNP_ID_732535933 m1A Human chrX + 135052100 135052100 135052100 CCGGCCAGGAGGGCCTTCATCAGCTGCACCCGACCGTCCATCGTGCCGCGCGCGCTCCGCGGAGT CCGGCCAGGAGGGCCTTCATCAGCTGCACCCGGCCGTCCATCGTGCCGCGCGCGCTCCGCGGAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:135051976..135052175 26863196 MeRIP-seq:(Medium) rs1419687152 Functional Loss SNV dbSNP153 33..33 33 - - - 85928 RMVar_ID_85928 Human_SNP_ID_732573967 m1A Human chrX - 135338966 135338966 135338966 GGAGAGAAGGGAGAGGAGGACAAGAAGGAGAAAAGCAAGGAGAAGAAGTAAAGGAGGAAGAATAG GGAGAGAAGGGAGAGGAGGACAAGAAGGAGAAGAGCAAGGAGAAGAAGTAAAGGAGGAAGAATAG T C ZNF75D Ensembl:ENSG00000186376 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:135338830..135339103 26863196 MeRIP-seq:(Medium) rs1233203266 Functional Loss SNV dbSNP153 33..33 33 - - - 85929 RMVar_ID_85929 Human_SNP_ID_732664026 m1A Human chrX + 135973969 135973969 135973969 AACGGAGTCATAAACGAAGAGGCGAAAGCGGGAGCTACGGGGAAGCGAAGAGGAAGGGCGCCGGC AACGGAGTCATAAACGAAGAGGCGAAAGCGGGCGCTACGGGGAAGCGAAGAGGAAGGGCGCCGGC A C SLC9A6 Ensembl:ENSG00000198689 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:135973663..135974063 26863196 MeRIP-seq:(Medium) rs1556612964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2238117 85930 RMVar_ID_85930 Human_SNP_ID_732666131 m1A Human chrX + 135985569 135985569 135985569 GCCGTGGCGTCGGCAGCAGTCCCCGAGCCCGCAGGCTCATGCGGCCCCTTTGGTTGCTCCTCGCA GCCGTGGCGTCGGCAGCAGTCCCCGAGCCCGCGGGCTCATGCGGCCCCTTTGGTTGCTCCTCGCA A G SLC9A6 Ensembl:ENSG00000198689 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:135985518..135985713 26863196 MeRIP-seq:(Medium) rs796053277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076779 RMVar_hsa_circ_22004 85931 RMVar_ID_85931 Human_SNP_ID_732694764 m1A Human chrX + 136147577 136147577 136147577 CCGCCGCCACCGCCGCGCCTCGGCCTCGGTGCAGGCAGCGGCCGCCGCCGCCGAGACAGCTGCGC CCGCCGCCACCGCCGCGCCTCGGCCTCGGTGCGGGCAGCGGCCGCCGCCGCCGAGACAGCTGCGC A G FHL1 Ensembl:ENSG00000022267 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136147459..136147681 26863196 MeRIP-seq:(Medium) rs1395905044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257825,Human_RBP_ID_729381,Human_RBP_ID_5053758 Human_Splice_Rec_2238483,Human_Splice_Rec_2238495,Human_Splice_Rec_2238503,Human_Splice_Rec_2238509,Human_Splice_Rec_2238523,Human_Splice_Rec_2238537 85932 RMVar_ID_85932 Human_SNP_ID_732708507 m1A Human chrX - 136225967 136225967 136225967 AATAAAAGCTCAAGAGGAAGCTGACAAACGCAAGAAAGAACACGAGAGAATTATGTTACAAAATT AATAAAAGCTCAAGAGGAAGCTGACAAACGCAGGAAAGAACACGAGAGAATTATGTTACAAAATT T C MAP7D3 Ensembl:ENSG00000129680 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:136224851..136228694;chrX:136222471..136228647;chrX:136222471..136228715 26863196 MeRIP-seq:(Medium) rs377561911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3244886,Human_RBP_ID_5659599 Human_Splice_Rec_2238807,Human_Splice_Rec_2238808,Human_Splice_Rec_2238846,Human_Splice_Rec_2238847,Human_Splice_Rec_2238880,Human_Splice_Rec_2238881,Human_Splice_Rec_2238913,Human_Splice_Rec_2238914,Human_Splice_Rec_2238923,Human_Splice_Rec_2238924,Human_Splice_Rec_2238932,Human_Splice_Rec_2238933 RMVar_hsa_circ_357636,RMVar_hsa_circ_55401,RMVar_hsa_circ_66988,RMVar_hsa_circ_345858,RMVar_hsa_circ_46477 85933 RMVar_ID_85933 Human_SNP_ID_732711878 m1A Human chrX - 136244687 136244685 136244688 GAGAAAGCTGAAGGAGCGAAAAGAGAAAGAAGAACAACGGAGAATAGCTGCAGAAGAAAAAAGAC GAGAAAGCTGAAGGAGCGAAAAGAGAAAGAA___CAACGGAGAATAGCTGCAGAAGAAAAAAGAC GTTC G MAP7D3 Ensembl:ENSG00000129680 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:136241247..136246070 26863196 MeRIP-seq:(Medium) rs1237816839 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_26364258,Human_RBP_ID_27144251 Human_Splice_Rec_2238793,Human_Splice_Rec_2238831,Human_Splice_Rec_2238864,Human_Splice_Rec_2238898 RMVar_hsa_circ_53434,RMVar_hsa_circ_55401,RMVar_hsa_circ_345858,RMVar_hsa_circ_342756,RMVar_hsa_circ_46477,RMVar_hsa_circ_352871,RMVar_hsa_circ_344128,RMVar_hsa_circ_309520,RMVar_hsa_circ_264016,RMVar_hsa_circ_365780 85934 RMVar_ID_85934 Human_SNP_ID_732711886 m1A Human chrX - 136244720 136244717 136244721 GCTCCAATATGAAAAACAGATGGAGGAAAGACAGAGAAAGCTGAAGGAGCGAAAAGAGAAAGAAG GCTCCAATATGAAAAACAGATGGAGGAAAGA____GAAAGCTGAAGGAGCGAAAAGAGAAAGAAG CTCTG C MAP7D3 Ensembl:ENSG00000129680 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136244670..136244748 26863196 MeRIP-seq:(Medium) rs1375162206 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_94846,Human_RBP_ID_3244902,Human_RBP_ID_5053902,Human_RBP_ID_26364258 Human_Splice_Rec_2238792,Human_Splice_Rec_2238793,Human_Splice_Rec_2238830,Human_Splice_Rec_2238831,Human_Splice_Rec_2238863,Human_Splice_Rec_2238864,Human_Splice_Rec_2238897,Human_Splice_Rec_2238898 RMVar_hsa_circ_53434,RMVar_hsa_circ_55401,RMVar_hsa_circ_345858,RMVar_hsa_circ_342756,RMVar_hsa_circ_46477,RMVar_hsa_circ_352871,RMVar_hsa_circ_344128,RMVar_hsa_circ_309520,RMVar_hsa_circ_264016,RMVar_hsa_circ_365780 85935 RMVar_ID_85935 Human_SNP_ID_732712187 m1A Human chrX - 136246326 136246326 136246326 ATCTCCCTGTATTTTAGTTGCTGCAGCAAACGAGATTGCTAAGGAAAGGAGGAAGCAAGATGTGG ATCTCCCTGTATTTTAGTTGCTGCAGCAAACGTGATTGCTAAGGAAAGGAGGAAGCAAGATGTGG T A MAP7D3 Ensembl:ENSG00000129680 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136246276..136246382 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_16829951,Human_RBP_ID_18916045 Human_Splice_Rec_2238788,Human_Splice_Rec_2238789,Human_Splice_Rec_2238826,Human_Splice_Rec_2238827,Human_Splice_Rec_2238859,Human_Splice_Rec_2238860,Human_Splice_Rec_2238893,Human_Splice_Rec_2238894 RMVar_hsa_circ_53434,RMVar_hsa_circ_344128,RMVar_hsa_circ_265802,RMVar_hsa_circ_365780 85936 RMVar_ID_85936 Human_SNP_ID_732757685 m1A Human chrX - 136497337 136497337 136497337 CCGCCGCCGCCACCGCCGCCGCCGCCGACCGGATCTGAGGCGACTGCGGCTCCCTCGGCAACGTC CCGCCGCCGCCACCGCCGCCGCCGCCGACCGGCTCTGAGGCGACTGCGGCTCCCTCGGCAACGTC T G lnc-ARHGEF6-5 RNACentral:URS0000D5D5BF lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:136497288..136497378 26863196 MeRIP-seq:(Medium) rs1030784664 Functional Loss SNV dbSNP153 33..33 33 - - - 85937 RMVar_ID_85937 Human_SNP_ID_732815580 m1A Human chrX - 136842134 136842134 136842134 CTGTAGTCCATGCTACTTGGGAGGCTGAGGCAAGAGGATTGCTCGAGCCCAGGAGGTTAAGGCTG CTGTAGTCCATGCTACTTGGGAGGCTGAGGCAGGAGGATTGCTCGAGCCCAGGAGGTTAAGGCTG T C AL683813.2 Ensembl:ENSG00000232611 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3180318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931532 RMVar_hsa_circ_264020 85938 RMVar_ID_85938 Human_SNP_ID_732822122 m1A Human chrX + 136870153 136870151 136870153 TAAACAAAATGAAAGCCAAAGCTGTAAAATCTATGTGAAGAACCACAAGAACTTCCTGACTACCT TAAACAAAATGAAAGCCAAAGCTGTAAAATC__TGTGAAGAACCACAAGAACTTCCTGACTACCT CTA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:136870152..136872302 32194978 MeRIP-seq:(Medium) rs763812971 Functional Loss DEL dbSNP153 32..33 33 - - - 85939 RMVar_ID_85939 Human_SNP_ID_732822124 m1A Human chrX + 136870153 136870153 136870153 TAAACAAAATGAAAGCCAAAGCTGTAAAATCTATGTGAAGAACCACAAGAACTTCCTGACTACCT TAAACAAAATGAAAGCCAAAGCTGTAAAATCTGTGTGAAGAACCACAAGAACTTCCTGACTACCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:136870152..136872302 32194978 MeRIP-seq:(Medium) rs1342691100 Functional Loss SNV dbSNP153 33..33 33 - - - 85940 RMVar_ID_85940 Human_SNP_ID_732823250 m1A Human chrX - 136874344 136874344 136874344 CAGCTCACGTGACGGATATGGTGGAAGTCGAGACAGTTACTCAAGCAGCCGAAGTGATCTCTACT CAGCTCACGTGACGGATATGGTGGAAGTCGAGGCAGTTACTCAAGCAGCCGAAGTGATCTCTACT T C RBMX Ensembl:ENSG00000147274 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1180043380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257484 RMVar_hsa_circ_264024,RMVar_hsa_circ_286408,RMVar_hsa_circ_367785 85941 RMVar_ID_85941 Human_SNP_ID_732823581 m1A Human chrX - 136875575 136875575 136875575 AAAAATGATATTTTTCCTTAAGCTCCTGTATCACGTGGAAGAGATAGTTATGGAGGTCCACCTCG AAAAATGATATTTTTCCTTAAGCTCCTGTATCGCGTGGAAGAGATAGTTATGGAGGTCCACCTCG T C RBMX Ensembl:ENSG00000147274 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs781656874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8713872,Human_RBP_ID_24331349 Human_Splice_Rec_2239313,Human_Splice_Rec_2239333,Human_Splice_Rec_2239347,Human_Splice_Rec_2239361,Human_Splice_Rec_2239377,Human_Splice_Rec_2239393,Human_Splice_Rec_2239403 Human_miRNA_ID_267285 RMVar_hsa_circ_5043,RMVar_hsa_circ_264024,RMVar_hsa_circ_286408,RMVar_hsa_circ_367785,RMVar_hsa_circ_108334,RMVar_hsa_circ_57228,RMVar_hsa_circ_264026 85942 RMVar_ID_85942 Human_SNP_ID_732823950 m1A Human chrX + 136876564 136876564 136876564 ACTGGTCCTGAAGGTGCAGATCTCTTAGGAGGAGGACCCCCACTTCTTGGTGGTGGTCCTCTTTT ACTGGTCCTGAAGGTGCAGATCTCTTAGGAGGTGGACCCCCACTTCTTGGTGGTGGTCCTCTTTT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:136875142..136876635 32194978 MeRIP-seq:(Medium) rs769574898 Functional Loss SNV dbSNP153 33..33 33 - - - 85943 RMVar_ID_85943 Human_SNP_ID_732825015 m1A Human chrX - 136879449 136879449 136879449 GTGAGGTAATACTATTCCTTTTCAACAGACTCACCGGCCCAAAAAAAAAAAAACATGGTTGAAGC GTGAGGTAATACTATTCCTTTTCAACAGACTCCCCGGCCCAAAAAAAAAAAAACATGGTTGAAGC T G RBMX Ensembl:ENSG00000147274 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136879383..136879485 26863196 MeRIP-seq:(Medium) rs954385748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967565,Human_RBP_ID_5054209,Human_RBP_ID_22632369 Human_Splice_Rec_2239309,Human_Splice_Rec_2239327,Human_Splice_Rec_2239355,Human_Splice_Rec_2239369,Human_Splice_Rec_2239385,Human_Splice_Rec_2239411,Human_Splice_Rec_2239419,Human_Splice_Rec_2239425 RMVar_hsa_circ_108334,RMVar_hsa_circ_80118,RMVar_hsa_circ_264026,RMVar_hsa_circ_264027 85944 RMVar_ID_85944 Human_SNP_ID_732825224 m1A Human chrX - 136880280 136880280 136880280 GCATTGGTATGGCGCTGGCGCTAATGATGGGCATGTGGACTTCCATGCGGGCTGCGGGCTTCGTA GCATTGGTATGGCGCTGGCGCTAATGATGGGCTTGTGGACTTCCATGCGGGCTGCGGGCTTCGTA T A RBMX Ensembl:ENSG00000147274 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:136880278..136880470 26863196 MeRIP-seq:(Medium) rs907204634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16832013 85945 RMVar_ID_85945 Human_SNP_ID_732825316 m1A Human chrX + 136880618 136880618 136880618 GAGACACGTACCGGAGGGGTGACAATGGGTTCAAGCTCCAACGAGCTCGGCGATAGGGGCTTCCT GAGACACGTACCGGAGGGGTGACAATGGGTTCGAGCTCCAACGAGCTCGGCGATAGGGGCTTCCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:136880594..136880690 26863410 MeRIP-seq:(Medium) rs1283271650 Functional Loss SNV dbSNP153 33..33 33 - - - 85946 RMVar_ID_85946 Human_SNP_ID_732825328 m1A Human chrX - 136880650 136880650 136880650 CACCCGGCAGCCGCCACTGGTGCTGAGCTGCTAGGAAGCCCCTATCGCCGAGCTCGTTGGAGCTT CACCCGGCAGCCGCCACTGGTGCTGAGCTGCTGGGAAGCCCCTATCGCCGAGCTCGTTGGAGCTT T C RBMX Ensembl:ENSG00000147274 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:136879321..136880725 32194978 MeRIP-seq:(Medium) rs903679077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_729677,Human_RBP_ID_1711726,Human_RBP_ID_5054212,Human_RBP_ID_5431932,Human_RBP_ID_5455239,Human_RBP_ID_7981143,Human_RBP_ID_18916152,Human_RBP_ID_22843438,Human_RBP_ID_27379648 Human_Splice_Rec_2239308,Human_Splice_Rec_2239326,Human_Splice_Rec_2239354,Human_Splice_Rec_2239368,Human_Splice_Rec_2239384,Human_Splice_Rec_2239398,Human_Splice_Rec_2239410,Human_Splice_Rec_2239418,Human_Splice_Rec_2239424 85947 RMVar_ID_85947 Human_SNP_ID_732825334 m1A Human chrX - 136880667 136880667 136880667 TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCACTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCTCTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC T A RBMX Ensembl:ENSG00000147274 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136880542..136880725 26863196 MeRIP-seq:(Medium) rs1243195018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_729677,Human_RBP_ID_5054212,Human_RBP_ID_5431932,Human_RBP_ID_18428060,Human_RBP_ID_18916152,Human_RBP_ID_22468993,Human_RBP_ID_24331363,Human_RBP_ID_27379648 Human_Splice_Rec_2239308,Human_Splice_Rec_2239326,Human_Splice_Rec_2239354,Human_Splice_Rec_2239368,Human_Splice_Rec_2239384,Human_Splice_Rec_2239398,Human_Splice_Rec_2239410,Human_Splice_Rec_2239418,Human_Splice_Rec_2239424 85948 RMVar_ID_85948 Human_SNP_ID_732825335 m1A Human chrX - 136880667 136880667 136880667 TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCACTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCGCTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC T C RBMX Ensembl:ENSG00000147274 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136880542..136880725 26863196 MeRIP-seq:(Medium) rs1243195018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_729677,Human_RBP_ID_5054212,Human_RBP_ID_5431932,Human_RBP_ID_18428060,Human_RBP_ID_18916152,Human_RBP_ID_22468993,Human_RBP_ID_24331363,Human_RBP_ID_27379648 Human_Splice_Rec_2239308,Human_Splice_Rec_2239326,Human_Splice_Rec_2239354,Human_Splice_Rec_2239368,Human_Splice_Rec_2239384,Human_Splice_Rec_2239398,Human_Splice_Rec_2239410,Human_Splice_Rec_2239418,Human_Splice_Rec_2239424 85949 RMVar_ID_85949 Human_SNP_ID_732825387 m1A Human chrX + 136880713 136880713 136880713 TGCGAGGACCGAACCGCGAAGCCGCTAGCACTACTGCGCAACGAGGGCGAACAAAGGAGACAGCA TGCGAGGACCGAACCGCGAAGCCGCTAGCACTGCTGCGCAACGAGGGCGAACAAAGGAGACAGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:136880701..136880725 26863196 MeRIP-seq:(Medium) rs903772774 Functional Loss SNV dbSNP153 33..33 33 - - - 85950 RMVar_ID_85950 Human_SNP_ID_733358932 m1A Human chrX + 139932608 139932608 139932608 CAGCCCGACACTACTCCCCTGTCTCTGTCGGGAGCCACAGCCTCCCTCGCCCCGGCCCTAACTCG CAGCCCGACACTACTCCCCTGTCTCTGTCGGGGGCCACAGCCTCCCTCGCCCCGGCCCTAACTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:139932052..139933025 26863196 MeRIP-seq:(Medium) rs1478340575 Functional Loss SNV dbSNP153 33..33 33 - - - 85951 RMVar_ID_85951 Human_SNP_ID_733358984 m1A Human chrX + 139932827 139932827 139932827 GGGCGTGGTGGAGCCGGGCTCTGAGGCAGGGCACCGTGAAGACCCCAGCGCGGGAGGGGCGGGGC GGGCGTGGTGGAGCCGGGCTCTGAGGCAGGGCCCCGTGAAGACCCCAGCGCGGGAGGGGCGGGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:139932351..139932948 32194978 MeRIP-seq:(Medium) rs1203418142 Functional Loss SNV dbSNP153 33..33 33 - - - 85952 RMVar_ID_85952 Human_SNP_ID_733507338 m1A Human chrX + 140777213 140777213 140777213 CCTAATGCATACGGGGCTTAAAACCTAGATGAAGGGTTGATGGGTGCAGCGAACCACCATGGCAC CCTAATGCATACGGGGCTTAAAACCTAGATGACGGGTTGATGGGTGCAGCGAACCACCATGGCAC A C LINC00632 Ensembl:ENSG00000203930 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:140777193..140777278 26863410 MeRIP-seq:(Medium) rs1362235797 Functional Loss SNV dbSNP153 33..33 33 - - - 85953 RMVar_ID_85953 Human_SNP_ID_733507339 m1A Human chrX + 140777213 140777213 140777213 CCTAATGCATACGGGGCTTAAAACCTAGATGAAGGGTTGATGGGTGCAGCGAACCACCATGGCAC CCTAATGCATACGGGGCTTAAAACCTAGATGAGGGGTTGATGGGTGCAGCGAACCACCATGGCAC A G LINC00632 Ensembl:ENSG00000203930 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:140777193..140777278 26863410 MeRIP-seq:(Medium) rs1362235797 Functional Loss SNV dbSNP153 33..33 33 - - - 85954 RMVar_ID_85954 Human_SNP_ID_733575355 m1A Human chrX - 141176237 141176237 141176237 TGGCCAGGCCCCTGTTACAAACTGCGCAGACCACCCGTAGCCCTGCTGCTGCCACCTGCCCTGCT TGGCCAGGCCCCTGTTACAAACTGCGCAGACCGCCCGTAGCCCTGCTGCTGCCACCTGCCCTGCT T C LDOC1 Ensembl:ENSG00000182195 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:141176044..141176301 26863196 MeRIP-seq:(Medium) rs1373732580 Functional Loss SNV dbSNP153 33..33 33 - - - 85955 RMVar_ID_85955 Human_SNP_ID_733575415 m1A Human chrX + 141176493 141176493 141176493 CGGGTAGGTAAGGGGACCGGAGGGCAAGGGGGAGAGCAGTGGCTCCTGGCGGGGTGAGGGCTGCG CGGGTAGGTAAGGGGACCGGAGGGCAAGGGGGGGAGCAGTGGCTCCTGGCGGGGTGAGGGCTGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:141176476..141176500 26863196 MeRIP-seq:(Medium) rs1556283411 Functional Loss SNV dbSNP153 33..33 33 - - - 85956 RMVar_ID_85956 Human_SNP_ID_733575438 m1A Human chrX - 141176553 141176553 141176553 ATTAGGCCCTCGACCCTCGGGCCTCGGGGGGGAGGGCCCTGCACGCCGCCACCCCCTCCCCGCAG ATTAGGCCCTCGACCCTCGGGCCTCGGGGGGGGGGGCCCTGCACGCCGCCACCCCCTCCCCGCAG T C LDOC1 Ensembl:ENSG00000182195 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:141176451..141176600 26863410 MeRIP-seq:(Medium) rs1556283433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27144650 85957 RMVar_ID_85957 Human_SNP_ID_733575527 m1A Human chrX - 141176894 141176894 141176894 GCTGGTGTGCGAGAGGGCCAGCCTGCTGCGCCAGGTACGTCCGCCGAGCTGCCCGGTGCCCTTCC GCTGGTGTGCGAGAGGGCCAGCCTGCTGCGCCGGGTACGTCCGCCGAGCTGCCCGGTGCCCTTCC T C LDOC1 Ensembl:ENSG00000182195 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:141176846..141177106 26863196 MeRIP-seq:(Medium) rs782366727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_730005 Human_Splice_Rec_2240484,Human_Splice_Rec_2240488 85958 RMVar_ID_85958 Human_SNP_ID_733575554 m1A Human chrX - 141177033 141177033 141177033 CCGAGCCGAACCGAGCCGAGTCCTGTCCTTCCAGGCCGTTCGCAATGGTGGATGAGTTGGTGCTG CCGAGCCGAACCGAGCCGAGTCCTGTCCTTCCGGGCCGTTCGCAATGGTGGATGAGTTGGTGCTG T C LDOC1 Ensembl:ENSG00000182195 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:141176928..141177090 26863196 MeRIP-seq:(Medium) rs1463736633 Functional Loss SNV dbSNP153 33..33 33 - - - 85959 RMVar_ID_85959 Human_SNP_ID_734829615 m1A Human chrX + 147912020 147912020 147912020 CCGACGGCGAGCGCGGGCGGCGGCGGTGACGGAGGCGCCGCTGCCAGGGGGCGTGCGGCAGCGCG CCGACGGCGAGCGCGGGCGGCGGCGGTGACGGCGGCGCCGCTGCCAGGGGGCGTGCGGCAGCGCG A C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chrX:147911930..147912154;chrX:147911926..147912127 26863410 MeRIP-seq:(Medium) rs868967873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257796,Human_RBP_ID_5076788,Human_RBP_ID_5535989,Human_RBP_ID_18427891 85960 RMVar_ID_85960 Human_SNP_ID_734829706 m1A Human chrX + 147912081 147912051 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGC______________________________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1385705433 Functional Loss DEL dbSNP153 4..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85961 RMVar_ID_85961 Human_SNP_ID_734829709 m1A Human chrX + 147912081 147912054 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGC___________________________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1182875085 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85962 RMVar_ID_85962 Human_SNP_ID_734829717 m1A Human chrX + 147912081 147912057 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGC________________________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1481009486 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85963 RMVar_ID_85963 Human_SNP_ID_734829725 m1A Human chrX + 147912081 147912060 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGC_____________________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1339187510 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85964 RMVar_ID_85964 Human_SNP_ID_734829732 m1A Human chrX + 147912081 147912063 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGC__________________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1305791118 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85965 RMVar_ID_85965 Human_SNP_ID_734829736 m1A Human chrX + 147912081 147912066 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGC_______________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1162637856 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85966 RMVar_ID_85966 Human_SNP_ID_734829742 m1A Human chrX + 147912081 147912069 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGCGGC____________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1419747486 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85967 RMVar_ID_85967 Human_SNP_ID_734829747 m1A Human chrX + 147912081 147912072 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGCGGCGGC_________GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1490888144 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85968 RMVar_ID_85968 Human_SNP_ID_734829752 m1A Human chrX + 147912081 147912075 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGCGGCGGCGGC______GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGCGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1354701418 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85969 RMVar_ID_85969 Human_SNP_ID_734829755 m1A Human chrX + 147912081 147912078 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGCGGCGGCGGCGGC___GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGGA C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1302149259 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85970 RMVar_ID_85970 Human_SNP_ID_734829763 m1A Human chrX + 147912081 147912081 147912081 CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG CGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTG A C FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chrX:147911901..147912747;chrX:147911966..147912092;chrX:147911965..147912095;chrX:147911951..147912200;chrX:147912000..147912150;chrX:147911907..147912268 26863196,26863410,26863196 MeRIP-seq:(Medium) rs868919729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_187799,Human_RBP_ID_257796,Human_RBP_ID_19027678 85971 RMVar_ID_85971 Human_SNP_ID_734856370 m1A Human chrX + 148052272 148052272 148052272 GCCAGAACTACCACCAGGACTCAGAGGCGGCCATCAACCGCCAGATCAACCTGGAGCTCTACGCC GCCAGAACTACCACCAGGACTCAGAGGCGGCCGTCAACCGCCAGATCAACCTGGAGCTCTACGCC A G FTH1P8 Ensembl:ENSG00000219507 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:148052049..148052278 26863196 MeRIP-seq:(Medium) rs1362649879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17328509,Human_RBP_ID_17556286,Human_RBP_ID_18204292,Human_RBP_ID_18213461,Human_RBP_ID_26835086 85972 RMVar_ID_85972 Human_SNP_ID_734856380 m1A Human chrX + 148052309 148052309 148052309 CCGCCAGATCAACCTGGAGCTCTACGCCTCCTACGTTTACCTGTCCATGTCTTACTACTTTGACC CCGCCAGATCAACCTGGAGCTCTACGCCTCCTCCGTTTACCTGTCCATGTCTTACTACTTTGACC A C FTH1P8 Ensembl:ENSG00000219507 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:148052223..148052315 26863410 MeRIP-seq:(Medium) rs782315342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9250306,Human_RBP_ID_17328509,Human_RBP_ID_17443251,Human_RBP_ID_17556286,Human_RBP_ID_26835087 Human_miRNA_ID_1862736,Human_miRNA_ID_1899395 85973 RMVar_ID_85973 Human_SNP_ID_734856381 m1A Human chrX + 148052309 148052309 148052309 CCGCCAGATCAACCTGGAGCTCTACGCCTCCTACGTTTACCTGTCCATGTCTTACTACTTTGACC CCGCCAGATCAACCTGGAGCTCTACGCCTCCTGCGTTTACCTGTCCATGTCTTACTACTTTGACC A G FTH1P8 Ensembl:ENSG00000219507 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:148052223..148052315 26863410 MeRIP-seq:(Medium) rs782315342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9250306,Human_RBP_ID_17328509,Human_RBP_ID_17443251,Human_RBP_ID_17556286,Human_RBP_ID_26835087 Human_miRNA_ID_1862736,Human_miRNA_ID_1899395 85974 RMVar_ID_85974 Human_SNP_ID_734938569 m1A Human chrX - 148500685 148500643 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_________________________________ CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1557231536 Functional Loss DEL dbSNP153 33..65 33 - - - 85975 RMVar_ID_85975 Human_SNP_ID_734938574 m1A Human chrX - 148500685 148500646 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_________________________________ CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1287478585 Functional Loss DEL dbSNP153 33..65 33 - - - 85976 RMVar_ID_85976 Human_SNP_ID_734938580 m1A Human chrX - 148500685 148500649 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_________________________________ CGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1435158925 Functional Loss DEL dbSNP153 33..65 33 - - - 85977 RMVar_ID_85977 Human_SNP_ID_734938590 m1A Human chrX - 148500685 148500658 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC___________________________GGCGGC CGCCGCCGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1190501824 Functional Loss DEL dbSNP153 33..59 33 - - - 85978 RMVar_ID_85978 Human_SNP_ID_734938601 m1A Human chrX - 148500685 148500664 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_____________________GGCGGCGGCGGC CGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1437983175 Functional Loss DEL dbSNP153 33..53 33 - - - 85979 RMVar_ID_85979 Human_SNP_ID_734938605 m1A Human chrX - 148500685 148500667 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC__________________GGCGGCGGCGGCGGC CGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1361216977 Functional Loss DEL dbSNP153 33..50 33 - - - 85980 RMVar_ID_85980 Human_SNP_ID_734938609 m1A Human chrX - 148500685 148500670 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_______________GGCGGCGGCGGCGGCGGC CGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1177058713 Functional Loss DEL dbSNP153 33..47 33 - - - 85981 RMVar_ID_85981 Human_SNP_ID_734938612 m1A Human chrX - 148500685 148500673 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC____________GGCGGCGGCGGCGGCGGCGGC CGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1186553278 Functional Loss DEL dbSNP153 33..44 33 - - - 85982 RMVar_ID_85982 Human_SNP_ID_734938616 m1A Human chrX - 148500685 148500676 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC_________GGCGGCGGCGGCGGCGGCGGCGGC CGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1310067407 Functional Loss DEL dbSNP153 33..41 33 - - - 85983 RMVar_ID_85983 Human_SNP_ID_734938623 m1A Human chrX - 148500685 148500679 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC______GGCGGCGGCGGCGGCGGCGGCGGCGGC CGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1297546925 Functional Loss DEL dbSNP153 33..38 33 - - - 85984 RMVar_ID_85984 Human_SNP_ID_734938627 m1A Human chrX - 148500685 148500682 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGC___GGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs1226744000 Functional Loss DEL dbSNP153 33..35 33 - - - 85985 RMVar_ID_85985 Human_SNP_ID_734938631 m1A Human chrX - 148500685 148500685 148500685 AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC AGGCAGCGGCGCGGCGCGGCAGCCGGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:148500614..148500719 26863196 MeRIP-seq:(Medium) rs868949662 Functional Loss SNV dbSNP153 33..33 33 - - - 85986 RMVar_ID_85986 Human_SNP_ID_735113169 m1A Human chrX - 149486941 149486941 149486941 TTCCCTTACCTCGACCCTTTTGATTCCGCCTCACAGTTGATGGAGCCAGGTATAAAATATGCTGA TTCCCTTACCTCGACCCTTTTGATTCCGCCTCGCAGTTGATGGAGCCAGGTATAAAATATGCTGA T C AC244197.3,IDS Ensembl:ENSG00000241489,Ensembl:ENSG00000010404 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:149483085..149486941 32194978 MeRIP-seq:(Medium) rs782363616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2241339,Human_Splice_Rec_2241438,Human_Splice_Rec_2241454,Human_Splice_Rec_2241458 RMVar_hsa_circ_37447,RMVar_hsa_circ_344626 85987 RMVar_ID_85987 Human_SNP_ID_735120880 m1A Human chrX - 149528545 149528545 149528545 AGAGGGAAAGAGAGGAGGAGAGGGAGAGAGGGAGAGAGAGGAAGGGAGGAAGGGGAAAGGAGAGG AGAGGGAAAGAGAGGAGGAGAGGGAGAGAGGGGGAGAGAGGAAGGGAGGAAGGGGAAAGGAGAGG T C LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149528344..149528673 26863196 MeRIP-seq:(Medium) rs5980481 Functional Loss SNV dbSNP153 33..33 33 - - - 85988 RMVar_ID_85988 Human_SNP_ID_735122177 m1A Human chrX - 149535125 149535122 149535125 AGAAGGAGGAGAGGAAGAGAGAAGGAAATGAGAAGGAGAAAAGTAGGAAGAAGAGAGAAGAGGAG AGAAGGAGGAGAGGAAGAGAGAAGGAAATGAG___GAGAAAAGTAGGAAGAAGAGAGAAGAGGAG CCTT C LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:149535114..149535253 26863196 MeRIP-seq:(Medium) rs1485899210 Functional Loss DEL dbSNP153 33..35 33 - - - 85989 RMVar_ID_85989 Human_SNP_ID_735122442 m1A Human chrX - 149535817 149535817 149535817 GAGAAGGAGAGGAGGAGGAGATGAGACCAAGGACAAGAGGTGAAGGAAGAGAGGAGGACACAGAA GAGAAGGAGAGGAGGAGGAGATGAGACCAAGGTCAAGAGGTGAAGGAAGAGAGGAGGACACAGAA T A LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:149534698..149536061;chrX:149535312..149535991 26863196 MeRIP-seq:(Medium) rs1421334488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931997,Human_RBP_ID_5108053,Human_RBP_ID_5233288,Human_RBP_ID_8226620 85990 RMVar_ID_85990 Human_SNP_ID_735122443 m1A Human chrX - 149535817 149535817 149535817 GAGAAGGAGAGGAGGAGGAGATGAGACCAAGGACAAGAGGTGAAGGAAGAGAGGAGGACACAGAA GAGAAGGAGAGGAGGAGGAGATGAGACCAAGGGCAAGAGGTGAAGGAAGAGAGGAGGACACAGAA T C LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:149534698..149536061;chrX:149535312..149535991 26863196 MeRIP-seq:(Medium) rs1421334488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931997,Human_RBP_ID_5108053,Human_RBP_ID_5233288,Human_RBP_ID_8226620 85991 RMVar_ID_85991 Human_SNP_ID_735122451 m1A Human chrX - 149535858 149535848 149535859 AGGGGGAGGAGAGGGAGTGGGTTGGAGGAGGGAAGGAGGAGGAGAAGGAGAGGAGGAGGAGATGA AGGGGGAGGAGAGGGAGTGGGTTGGAGGAGG___________AGAAGGAGAGGAGGAGGAGATGA TCCTCCTCCTTC T LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:149535710..149535918 26863196 MeRIP-seq:(Medium) rs1557344858 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_848349,Human_RBP_ID_1720062,Human_RBP_ID_8226620 85992 RMVar_ID_85992 Human_SNP_ID_735122524 m1A Human chrX - 149536121 149536121 149536121 TGGAGTGTCCCACTGCCCCTCCATCTGGAGGCAGTGACCCCTCTCCCACAGAGGAGGTGCTCGCA TGGAGTGTCCCACTGCCCCTCCATCTGGAGGCTGTGACCCCTCTCCCACAGAGGAGGTGCTCGCA T A LINC00893,AC244197.3 Ensembl:ENSG00000241769,Ensembl:ENSG00000241489 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:149536080..149536164 26863196 MeRIP-seq:(Medium) rs1343609840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2241419,Human_Splice_Rec_2241530,Human_Splice_Rec_2241565 85993 RMVar_ID_85993 Human_SNP_ID_735123214 m1A Human chrX + 149539690 149539690 149539690 CTTTCCTCCAGCTCTGCACTAGCTCCTCCCCCACCATTCTCACCCGCCAGCCTTACTCCAGCTTG CTTTCCTCCAGCTCTGCACTAGCTCCTCCCCCCCCATTCTCACCCGCCAGCCTTACTCCAGCTTG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:149539662..149539791 26863196 MeRIP-seq:(Medium) rs1350771918 Functional Loss SNV dbSNP153 33..33 33 - - - 85994 RMVar_ID_85994 Human_SNP_ID_735123215 m1A Human chrX + 149539690 149539690 149539690 CTTTCCTCCAGCTCTGCACTAGCTCCTCCCCCACCATTCTCACCCGCCAGCCTTACTCCAGCTTG CTTTCCTCCAGCTCTGCACTAGCTCCTCCCCCGCCATTCTCACCCGCCAGCCTTACTCCAGCTTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:149539662..149539791 26863196 MeRIP-seq:(Medium) rs1350771918 Functional Loss SNV dbSNP153 33..33 33 - - - 85995 RMVar_ID_85995 Human_SNP_ID_735124312 m1A Human chrX + 149544477 149544477 149544477 CAAGGGTGGAGTTCAGGGCCGGGGGCGGGGCCACGGGCCTGAGGGGTGAGGGCAGCCACTATTTC CAAGGGTGGAGTTCAGGGCCGGGGGCGGGGCCCCGGGCCTGAGGGGTGAGGGCAGCCACTATTTC A C EOLA1 Ensembl:ENSG00000197620 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149544437..149544528 26863196 MeRIP-seq:(Medium) rs1266741889 Functional Loss SNV dbSNP153 33..33 33 - - - 85996 RMVar_ID_85996 Human_SNP_ID_735124313 m1A Human chrX + 149544477 149544477 149544477 CAAGGGTGGAGTTCAGGGCCGGGGGCGGGGCCACGGGCCTGAGGGGTGAGGGCAGCCACTATTTC CAAGGGTGGAGTTCAGGGCCGGGGGCGGGGCCGCGGGCCTGAGGGGTGAGGGCAGCCACTATTTC A G EOLA1 Ensembl:ENSG00000197620 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149544437..149544528 26863196 MeRIP-seq:(Medium) rs1266741889 Functional Loss SNV dbSNP153 33..33 33 - - - 85997 RMVar_ID_85997 Human_SNP_ID_735131358 m1A Human chrX + 149604601 149604601 149604601 CCTAGCAGCACAGAAATGACTCCTTCTCATTAAAAACAAAAGCCCCGAAACCAGATAAACCCACC CCTAGCAGCACAGAAATGACTCCTTCTCATTAGAAACAAAAGCCCCGAAACCAGATAAACCCACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149604598..149604696 26863196 MeRIP-seq:(Medium) rs1380472459 Functional Loss SNV dbSNP153 33..33 33 - - - 85998 RMVar_ID_85998 Human_SNP_ID_735131590 m1A Human chrX - 149605418 149605414 149605418 ATGGGAGGCCATAGTGACATGGGAGGCCATAGAAAGTGACATGGGAGGCTATAGAAAGTGACATG ATGGGAGGCCATAGTGACATGGGAGGCCATAG____TGACATGGGAGGCTATAGAAAGTGACATG ACTTT A TMEM185A Ensembl:ENSG00000269556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149605415..149605509 26863196 MeRIP-seq:(Medium) rs1167372921 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_336321 85999 RMVar_ID_85999 Human_SNP_ID_735131822 m1A Human chrX - 149606544 149606544 149606544 CGATTCAGATCCGACGGGAGCACAAGGTGGAAAGGAAGGAACTGTGGGAGTTGAGAAGAGAGGGA CGATTCAGATCCGACGGGAGCACAAGGTGGAAGGGAAGGAACTGTGGGAGTTGAGAAGAGAGGGA T C TMEM185A Ensembl:ENSG00000269556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149606526..149606604 26863196 MeRIP-seq:(Medium) rs782104255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336321 86000 RMVar_ID_86000 Human_SNP_ID_735135919 m1A Human chrX - 149631723 149631706 149631724 CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA CGGCGGCGGCGGCGGCGGCGACGGCGACGGC__________________AGCAGTAGCGGGAGCA TGCCGTCCCCGCTGCCGTC T TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:149631666..149631782 26863410 MeRIP-seq:(Medium) rs1557356693 Functional Loss DEL dbSNP153 32..49 33 - - - Human_RBP_ID_5076791 86001 RMVar_ID_86001 Human_SNP_ID_735135920 m1A Human chrX - 149631706 149631706 149631706 GCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCAGCAGCGTGGACGCGGCT GCGACGGCGACGGCGACGGCAGCGGGGACGGCGGCAGTAGCGGGAGCAGCAGCGTGGACGCGGCT T C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:149631549..149631790 26863196 MeRIP-seq:(Medium) rs1569561125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5055038 86002 RMVar_ID_86002 Human_SNP_ID_735135925 m1A Human chrX - 149631711 149631711 149631711 CGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCAGCAGCGTGGACG CGGCGGCGACGGCGACGGCGACGGCAGCGGGGTCGGCAGCAGTAGCGGGAGCAGCAGCGTGGACG T A TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149631515..149631791 26863196 MeRIP-seq:(Medium) rs868957337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5055038 86003 RMVar_ID_86003 Human_SNP_ID_735135926 m1A Human chrX - 149631711 149631711 149631711 CGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCAGCAGCGTGGACG CGGCGGCGACGGCGACGGCGACGGCAGCGGGGGCGGCAGCAGTAGCGGGAGCAGCAGCGTGGACG T C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149631515..149631791 26863196 MeRIP-seq:(Medium) rs868957337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5055038 86004 RMVar_ID_86004 Human_SNP_ID_735135932 m1A Human chrX - 149631735 149631714 149631735 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCA CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG_____________________GGGACGGCAGCA CCGCTGCCGTCGCCGTCGCCGT C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:149611336..149631805;chrX:149631637..149631750;chrX:149631726..149631800 26863196 MeRIP-seq:(Medium) rs1474320090 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_5076791 86005 RMVar_ID_86005 Human_SNP_ID_735135935 m1A Human chrX - 149631723 149631717 149631723 CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA CGGCGGCGGCGGCGGCGGCGACGGCGACGGCG______GCGGGGACGGCAGCAGTAGCGGGAGCA CTGCCGT C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:149631666..149631782 26863410 MeRIP-seq:(Medium) rs1206188015 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_5076791 86006 RMVar_ID_86006 Human_SNP_ID_735135947 m1A Human chrX - 149631723 149631723 149631723 CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGGCGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA T C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:149631666..149631782 26863410 MeRIP-seq:(Medium) rs868927082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076791 86007 RMVar_ID_86007 Human_SNP_ID_735135985 m1A Human chrX - 149631735 149631730 149631735 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCA CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG_____GACGGCGACGGCAGCGGGGACGGCAGCA CGCCGT C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:149611336..149631805;chrX:149631637..149631750;chrX:149631726..149631800 26863196 MeRIP-seq:(Medium) rs1557356752 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_5076791 86008 RMVar_ID_86008 Human_SNP_ID_735135986 m1A Human chrX - 149631735 149631732 149631735 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCA CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCG___GCGACGGCGACGGCAGCGGGGACGGCAGCA CCGT C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:149611336..149631805;chrX:149631637..149631750;chrX:149631726..149631800 26863196 MeRIP-seq:(Medium) rs1210075716 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5076791 86009 RMVar_ID_86009 Human_SNP_ID_735135990 m1A Human chrX - 149631735 149631735 149631735 CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCA CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGACGGCAGCGGGGACGGCAGCA T C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chrX:149611336..149631805;chrX:149631637..149631750;chrX:149631726..149631800 26863196 MeRIP-seq:(Medium) rs182166465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076791 86010 RMVar_ID_86010 Human_SNP_ID_735147608 m1A Human chrX - 149712140 149712140 149712140 CAGCTCTCACCTTGCCTCCTCATGGAGCCTGGACCCGCTGCCCTCTGCCACTCTCAAGACACCCC CAGCTCTCACCTTGCCTCCTCATGGAGCCTGGGCCCGCTGCCCTCTGCCACTCTCAAGACACCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:149712089..149713204 26863196 MeRIP-seq:(Medium) rs1203306939 Functional Loss SNV dbSNP153 33..33 33 - - - 86011 RMVar_ID_86011 Human_SNP_ID_735180465 m1A Human chrX - 149935041 149935040 149935041 GTAGGGGCAGCTCAAGGGTGGAGTTCAGGGCCAGGGGGCGGGGCCACGGGCCTGAGGGGTGAGGG GTAGGGGCAGCTCAAGGGTGGAGTTCAGGGCC_GGGGGCGGGGCCACGGGCCTGAGGGGTGAGGG CT C EOLA2 Ensembl:ENSG00000197021 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:149934947..149935093 26863196 MeRIP-seq:(Medium) rs782025249 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3930386,Human_RBP_ID_9443545 86012 RMVar_ID_86012 Human_SNP_ID_735180670 m1A Human chrX - 149935818 149935818 149935818 GGGCAGAGAGCAGCTAGGTCTGGGGCAGGAACACTGTAGCTGGTGATGCCACTCACAGAGGTGGA GGGCAGAGAGCAGCTAGGTCTGGGGCAGGAACGCTGTAGCTGGTGATGCCACTCACAGAGGTGGA T C EOLA2 Ensembl:ENSG00000197021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149935611..149935941 26863196 MeRIP-seq:(Medium) rs28412769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17203776,Human_RBP_ID_22631370 86013 RMVar_ID_86013 Human_SNP_ID_735182110 m1A Human chrX + 149940080 149940080 149940080 AGATGGGGCGGGGCTGCGGGAAAGAGCTGGAGAAGGAGGAGCCAAGCTGCACCAAGGCTGGCGGG AGATGGGGCGGGGCTGCGGGAAAGAGCTGGAGGAGGAGGAGCCAAGCTGCACCAAGGCTGGCGGG A G LINC00894 Ensembl:ENSG00000235703 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:149939893..149940079 26863196 MeRIP-seq:(Medium) rs782495019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930400,Human_RBP_ID_8164645,Human_RBP_ID_8226631,Human_RBP_ID_8944869,Human_RBP_ID_9443211,Human_RBP_ID_17203780,Human_RBP_ID_18963699 Human_Splice_Rec_2241980,Human_Splice_Rec_2241982 Human_miRNA_ID_3150799,Human_miRNA_ID_3194557 86014 RMVar_ID_86014 Human_SNP_ID_735182214 m1A Human chrX - 149940321 149940321 149940321 CTTGCAGGCGGCTCCTCCAGAAGCTCTGACCCAGTCCCCGCTGCAGCCACAGCCCCAGCTTCTTA CTTGCAGGCGGCTCCTCCAGAAGCTCTGACCCCGTCCCCGCTGCAGCCACAGCCCCAGCTTCTTA T G lnc-CXorf40B-4-002 RNACentral:URS00008B251E lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:149939737..149940600 26863196 MeRIP-seq:(Medium) rs781788490 Functional Loss SNV dbSNP153 33..33 33 - - - 86015 RMVar_ID_86015 Human_SNP_ID_735182239 m1A Human chrX - 149940407 149940389 149940407 GCCCCAGCTATTCCGACGCCAGCCCCTGCTCCACCCGGCACTTAACCATTTCCGCCCACAGCTCT GCCCCAGCTATTCCGACGCCAGCCCCTGCTCC__________________TCCGCCCACAGCTCT AAATGGTTAAGTGCCGGGT A lnc-CXorf40B-4-002 RNACentral:URS00008B251E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149939399..149940795 26863196 MeRIP-seq:(Medium) rs1557377543 Functional Loss DEL dbSNP153 33..50 33 - - - 86016 RMVar_ID_86016 Human_SNP_ID_735182245 m1A Human chrX - 149940407 149940404 149940407 GCCCCAGCTATTCCGACGCCAGCCCCTGCTCCACCCGGCACTTAACCATTTCCGCCCACAGCTCT GCCCCAGCTATTCCGACGCCAGCCCCTGCTCC___CGGCACTTAACCATTTCCGCCCACAGCTCT GGGT G lnc-CXorf40B-4-002 RNACentral:URS00008B251E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149939399..149940795 26863196 MeRIP-seq:(Medium) rs1557377554 Functional Loss DEL dbSNP153 33..35 33 - - - 86017 RMVar_ID_86017 Human_SNP_ID_735182246 m1A Human chrX - 149940407 149940407 149940407 GCCCCAGCTATTCCGACGCCAGCCCCTGCTCCACCCGGCACTTAACCATTTCCGCCCACAGCTCT GCCCCAGCTATTCCGACGCCAGCCCCTGCTCCCCCCGGCACTTAACCATTTCCGCCCACAGCTCT T G lnc-CXorf40B-4-002 RNACentral:URS00008B251E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149939399..149940795 26863196 MeRIP-seq:(Medium) rs1263515515 Functional Loss SNV dbSNP153 33..33 33 - - - 86018 RMVar_ID_86018 Human_SNP_ID_51854995 m1A Human chr1 + 225428019 225428019 225428019 CCCGGAGAATAGTCGCACAGCAACCCGGCGGCAGATCCACGCGCGCGACGCTACCCGGCCGCGCT CCCGGAGAATAGTCGCACAGCAACCCGGCGGCGGATCCACGCGCGCGACGCTACCCGGCCGCGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Wild Type;HEPG2 cell line,mRNA Glucose starvation 4h chr1:225427951..225428100;chr1:225427851..225428727 26863410,26863196 MeRIP-seq:(Medium) rs1193116880 Functional Loss SNV dbSNP153 33..33 33 - - - 86019 RMVar_ID_86019 Human_SNP_ID_51860512 m1A Human chr1 - 225451096 225451096 225451096 GCCCTGAGGTGGAATCCAACAGCACGGAGGCCACTGTGGCTAGAGCTGAGTGAGCAGAAGGAAGA GCCCTGAGGTGGAATCCAACAGCACGGAGGCCGCTGTGGCTAGAGCTGAGTGAGCAGAAGGAAGA T C LINC02765 Ensembl:ENSG00000234476 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:225451094..225451210 26863196 MeRIP-seq:(Medium) rs772343817 Functional Loss SNV dbSNP153 33..33 33 - - - 86020 RMVar_ID_86020 Human_SNP_ID_51875845 m1A Human chr1 - 225514840 225514840 225514840 ACCTCCTCCACCACTCCCACCAGGGCCTGCACAGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC ACCTCCTCCACCACTCCCACCAGGGCCTGCACTGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC T A ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225514652..225514919 26863196 MeRIP-seq:(Medium) rs745538039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072557,Human_RBP_ID_22420324,Human_RBP_ID_26854631 Human_Splice_Rec_192592,Human_Splice_Rec_192638,Human_Splice_Rec_192664 Human_miRNA_ID_1368411,Human_miRNA_ID_2688653,Human_miRNA_ID_2691816 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_49029,RMVar_hsa_circ_16234,RMVar_hsa_circ_15278,RMVar_hsa_circ_336099,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746 86021 RMVar_ID_86021 Human_SNP_ID_51875846 m1A Human chr1 - 225514840 225514840 225514840 ACCTCCTCCACCACTCCCACCAGGGCCTGCACAGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC ACCTCCTCCACCACTCCCACCAGGGCCTGCACGGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC T C ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225514652..225514919 26863196 MeRIP-seq:(Medium) rs745538039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072557,Human_RBP_ID_22420324,Human_RBP_ID_26854631 Human_Splice_Rec_192592,Human_Splice_Rec_192638,Human_Splice_Rec_192664 Human_miRNA_ID_1368411,Human_miRNA_ID_2688653,Human_miRNA_ID_2691816 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_49029,RMVar_hsa_circ_16234,RMVar_hsa_circ_15278,RMVar_hsa_circ_336099,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746 86022 RMVar_ID_86022 Human_SNP_ID_51875847 m1A Human chr1 - 225514840 225514840 225514840 ACCTCCTCCACCACTCCCACCAGGGCCTGCACAGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC ACCTCCTCCACCACTCCCACCAGGGCCTGCACCGGCTTCAGTAGCCCTCCCTCCTCCCCCAGGGC T G ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225514652..225514919 26863196 MeRIP-seq:(Medium) rs745538039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072557,Human_RBP_ID_22420324,Human_RBP_ID_26854631 Human_Splice_Rec_192592,Human_Splice_Rec_192638,Human_Splice_Rec_192664 Human_miRNA_ID_1368411,Human_miRNA_ID_2688653,Human_miRNA_ID_2691816 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_49029,RMVar_hsa_circ_16234,RMVar_hsa_circ_15278,RMVar_hsa_circ_336099,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746 86023 RMVar_ID_86023 Human_SNP_ID_51875852 m1A Human chr1 - 225514851 225514851 225514851 CTTGCACCTCCACCTCCTCCACCACTCCCACCAGGGCCTGCACAGGCTTCAGTAGCCCTCCCTCC CTTGCACCTCCACCTCCTCCACCACTCCCACCGGGGCCTGCACAGGCTTCAGTAGCCCTCCCTCC T C ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:225514801..225514973 26863196 MeRIP-seq:(Medium) rs773781396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21784,Human_RBP_ID_22420324,Human_RBP_ID_26854631,Human_RBP_ID_27394433 Human_Splice_Rec_192592,Human_Splice_Rec_192638,Human_Splice_Rec_192664 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_49029,RMVar_hsa_circ_16234,RMVar_hsa_circ_15278,RMVar_hsa_circ_336099,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746 86024 RMVar_ID_86024 Human_SNP_ID_51876978 m1A Human chr1 - 225519283 225519283 225519283 AGACAAGAACGAGAGAGGCTGGAGAGACTGGAACGGGAGAGGCAAGAAAGGGAGCGACAAGAGCA AGACAAGAACGAGAGAGGCTGGAGAGACTGGATCGGGAGAGGCAAGAAAGGGAGCGACAAGAGCA T A ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:225519161..225567312 32194978 MeRIP-seq:(Medium) rs201461224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21787,Human_RBP_ID_222446,Human_RBP_ID_5162205,Human_RBP_ID_5537411,Human_RBP_ID_5766968,Human_RBP_ID_8744070,Human_RBP_ID_9357574,Human_RBP_ID_10804459,Human_RBP_ID_18966443,Human_RBP_ID_23368192,Human_RBP_ID_27394436 Human_Splice_Rec_192589,Human_Splice_Rec_192635,Human_Splice_Rec_192661 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 86025 RMVar_ID_86025 Human_SNP_ID_51876983 m1A Human chr1 - 225519304 225519304 225519304 CTGGATCGGGAGAGGCAAGAAAGACAAGAACGAGAGAGGCTGGAGAGACTGGAACGGGAGAGGCA CTGGATCGGGAGAGGCAAGAAAGACAAGAACGTGAGAGGCTGGAGAGACTGGAACGGGAGAGGCA T A ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:225519176..225519575;chr1:225519162..225519550 26863196 MeRIP-seq:(Medium) rs747052251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21787,Human_RBP_ID_222446,Human_RBP_ID_1122853,Human_RBP_ID_5766968,Human_RBP_ID_8300132,Human_RBP_ID_9357574,Human_RBP_ID_10804459,Human_RBP_ID_18966443,Human_RBP_ID_22855967,Human_RBP_ID_23368192,Human_RBP_ID_24646126 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 86026 RMVar_ID_86026 Human_SNP_ID_51876989 m1A Human chr1 - 225519313 225519313 225519313 CAGGAACGCCTGGATCGGGAGAGGCAAGAAAGACAAGAACGAGAGAGGCTGGAGAGACTGGAACG CAGGAACGCCTGGATCGGGAGAGGCAAGAAAGGCAAGAACGAGAGAGGCTGGAGAGACTGGAACG T C ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:225519224..225519516 26863196 MeRIP-seq:(Medium) rs1426440713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21787,Human_RBP_ID_222446,Human_RBP_ID_1122853,Human_RBP_ID_8300132,Human_RBP_ID_9357574,Human_RBP_ID_10804460,Human_RBP_ID_18966443,Human_RBP_ID_22855967,Human_RBP_ID_23117582,Human_RBP_ID_23368192,Human_RBP_ID_24646126 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 86027 RMVar_ID_86027 Human_SNP_ID_51877031 m1A Human chr1 - 225519359 225519357 225519359 CCTGGAGCGGCAGGAACGCCTGGAGCGGCAGGAACGCCTGGAGCGGCAGGAACGCCTGGATCGGG CCTGGAGCGGCAGGAACGCCTGGAGCGGCAGG__CGCCTGGAGCGGCAGGAACGCCTGGATCGGG GTT G ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:225519261..225519512 26863410 MeRIP-seq:(Medium) rs1558744091 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9357575,Human_RBP_ID_23117582,Human_RBP_ID_23368192 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 86028 RMVar_ID_86028 Human_SNP_ID_51877084 m1A Human chr1 - 225519431 225519431 225519431 AAGGCTGGAGAGGGAGCGACTGGAACAAGAACAGCTGGAGAGAGAGAGACAAGAACGGGAACGGC AAGGCTGGAGAGGGAGCGACTGGAACAAGAACGGCTGGAGAGAGAGAGACAAGAACGGGAACGGC T C ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:225519111..225530650 26863196 MeRIP-seq:(Medium) rs767019161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21788,Human_RBP_ID_8300134,Human_RBP_ID_9357576,Human_RBP_ID_10804464,Human_RBP_ID_22855969,Human_RBP_ID_23117582,Human_RBP_ID_23368192,Human_RBP_ID_24541557 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 86029 RMVar_ID_86029 Human_SNP_ID_51888495 m1A Human chr1 - 225567358 225567358 225567358 AGCTGCTGTGATGGTTTATGATGATGCCAATAAGAAGTGGGTGCCAGCTGGTGGCTCAACTGGAT AGCTGCTGTGATGGTTTATGATGATGCCAATAGGAAGTGGGTGCCAGCTGGTGGCTCAACTGGAT T C ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:225567307..225567454 26863196 MeRIP-seq:(Medium) rs1386262906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21795,Human_RBP_ID_856943,Human_RBP_ID_1422179,Human_RBP_ID_1738389,Human_RBP_ID_4089790,Human_RBP_ID_9357577,Human_RBP_ID_17676706,Human_RBP_ID_22855986,Human_RBP_ID_23368272,Human_RBP_ID_27176580 Human_Splice_Rec_192582,Human_Splice_Rec_192626,Human_Splice_Rec_192654,Human_Splice_Rec_192698,Human_Splice_Rec_192706 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_365726,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688,RMVar_hsa_circ_285345,RMVar_hsa_circ_140048,RMVar_hsa_circ_140045,RMVar_hsa_circ_140047,RMVar_hsa_circ_292308,RMVar_hsa_circ_375143 86030 RMVar_ID_86030 Human_SNP_ID_51888500 m1A Human chr1 + 225567414 225567414 225567414 ACAGCAGCTCTTGCCTGACAGATACTCTGTTCACTGTAAAAAATAAAATAAAATATTCAAACTTG ACAGCAGCTCTTGCCTGACAGATACTCTGTTCGCTGTAAAAAATAAAATAAAATATTCAAACTTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:225567411..225652692 32194978 MeRIP-seq:(Medium) rs373018201 Functional Loss SNV dbSNP153 33..33 33 - - - 86031 RMVar_ID_86031 Human_SNP_ID_51909487 m1A Human chr1 - 225652978 225652978 225652978 CAGAGGGCGGCCGAGGAAGCTCCGGGAGGAGGAGCAGGACCACGAGGAGGTGGGAGGCGGCGGCC CAGAGGGCGGCCGAGGAAGCTCCGGGAGGAGGCGCAGGACCACGAGGAGGTGGGAGGCGGCGGCC T G ENAH Ensembl:ENSG00000154380 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:225652751..225653086 26863196 MeRIP-seq:(Medium) rs1369477685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273381,Human_RBP_ID_4073292,Human_RBP_ID_5767655,Human_RBP_ID_9357580,Human_RBP_ID_26854724 Human_miRNA_ID_2867067 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 86032 RMVar_ID_86032 Human_SNP_ID_51909500 m1A Human chr1 - 225653062 225653040 225653062 CGGTTGCACACGGCCTCGGCGGCGGCGCGGCGAGCGCGGGCCTGTGGAGCGGCGGCCGGGCGCGC CGGTTGCACACGGCCTCGGCGGCGGCGCGGCG______________________GCCGGGCGCGC CCGCCGCTCCACAGGCCCGCGCT C ENAH Ensembl:ENSG00000154380 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:225652741..225653125;chr1:225652741..225653142;chr1:225652751..225653173;chr1:225652758..225653125 26863196 MeRIP-seq:(Medium) rs1370736727 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_222451,Human_RBP_ID_743452,Human_RBP_ID_4076403,Human_RBP_ID_9357580 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 86033 RMVar_ID_86033 Human_SNP_ID_51909522 m1A Human chr1 + 225653091 225653091 225653091 CGCTCGCCGCGCCGCCGCCGAGGCCGTGTGCAACCGGCAGCTGCTGCAGCCGCGGGAGGAGAGTC CGCTCGCCGCGCCGCCGCCGAGGCCGTGTGCACCCGGCAGCTGCTGCAGCCGCGGGAGGAGAGTC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:225652991..225653092 26863410 MeRIP-seq:(Medium) rs1232587707 Functional Loss SNV dbSNP153 33..33 33 - - - 86034 RMVar_ID_86034 Human_SNP_ID_51944980 m1A Human chr1 + 225796517 225796517 225796517 TGGGAGGTGGAGGTTGTAGCGAGCCGAGATCAAGCCACTGCACTCCAGCCTAGGCAACACTGAGC TGGGAGGTGGAGGTTGTAGCGAGCCGAGATCATGCCACTGCACTCCAGCCTAGGCAACACTGAGC A T lnc-SRP9-3 RNACentral:URS0000D59787 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:225796506..225796651 26863196 MeRIP-seq:(Medium) rs1165360508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10808196 86035 RMVar_ID_86035 Human_SNP_ID_51948809 m1A Human chr1 + 225810152 225810152 225810152 AGCCGGAGAGATCGCGCGCCTGCCGCCGCCGGAGCCTGCGAGCCGAGACCGTAAGCGCCCGGGGC AGCCGGAGAGATCGCGCGCCTGCCGCCGCCGGGGCCTGCGAGCCGAGACCGTAAGCGCCCGGGGC A G EPHX1 Ensembl:ENSG00000143819 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:225810101..225810360 26863196 MeRIP-seq:(Medium) rs956849112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745129,Human_RBP_ID_4074781,Human_RBP_ID_22429995 Human_Splice_Rec_192783,Human_Splice_Rec_192789 86036 RMVar_ID_86036 Human_SNP_ID_51948816 m1A Human chr1 + 225810165 225810165 225810165 GCGCGCCTGCCGCCGCCGGAGCCTGCGAGCCGAGACCGTAAGCGCCCGGGGCCGGCCGGGCCCGC GCGCGCCTGCCGCCGCCGGAGCCTGCGAGCCGGGACCGTAAGCGCCCGGGGCCGGCCGGGCCCGC A G EPHX1 Ensembl:ENSG00000143819 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:225810101..225810553;chr1:225810101..225810337 26863196 MeRIP-seq:(Medium) rs1260151446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074781,Human_RBP_ID_22429995 Human_Splice_Rec_192783,Human_Splice_Rec_192789 86037 RMVar_ID_86037 Human_SNP_ID_51953312 m1A Human chr1 - 225828822 225828822 225828822 GCTGCGGACCTCGTGCCTGGCCCCCACCACCCATCTTCAAGTGGCAAAGTTTCCTCTTTGTCCCG GCTGCGGACCTCGTGCCTGGCCCCCACCACCCGTCTTCAAGTGGCAAAGTTTCCTCTTTGTCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225828726..225828925 26863196 MeRIP-seq:(Medium) rs1347161321 Functional Loss SNV dbSNP153 33..33 33 - - - 86038 RMVar_ID_86038 Human_SNP_ID_51953335 m1A Human chr1 - 225828872 225828872 225828872 CCTCATCTGACGTTTCCACCTTGAAAGGGCGGATGCTGTCGTCCTCCCTGGCTGCGGACCTCGTG CCTCATCTGACGTTTCCACCTTGAAAGGGCGGGTGCTGTCGTCCTCCCTGGCTGCGGACCTCGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:225828851..225828875 26863196 MeRIP-seq:(Medium) rs1001038471 Functional Loss SNV dbSNP153 33..33 33 - - - 86039 RMVar_ID_86039 Human_SNP_ID_51962644 m1A Human chr1 - 225861419 225861419 225861419 AGATGGTGAGGGTCGAGGTGGGAGCCCTGAGGAGGGAAGCTTGGGAACAGGCAATGTGTAACGTG AGATGGTGAGGGTCGAGGTGGGAGCCCTGAGGCGGGAAGCTTGGGAACAGGCAATGTGTAACGTG T G TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:225861370..225861526 26863196 MeRIP-seq:(Medium) rs1014767979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259070,Human_RBP_ID_803909,Human_RBP_ID_850878,Human_RBP_ID_1064349,Human_RBP_ID_3934572,Human_RBP_ID_5332308,Human_RBP_ID_9412160,Human_RBP_ID_19035956,Human_RBP_ID_22635051 RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_360817,RMVar_hsa_circ_339883 86040 RMVar_ID_86040 Human_SNP_ID_51966583 m1A Human chr1 - 225876136 225876131 225876136 GGTGGGTATTGTTGCAACAGTGTTGGCTGAGAAGAGAGTCACCCTCTATTGTGCTGCTGAAGGTG GGTGGGTATTGTTGCAACAGTGTTGGCTGAGA_____GTCACCCTCTATTGTGCTGCTGAAGGTG CTCTCT C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:225876133..225876267 26863196 MeRIP-seq:(Medium) rs1285899116 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_5768187 RMVar_hsa_circ_55460,RMVar_hsa_circ_78561,RMVar_hsa_circ_33471,RMVar_hsa_circ_104024,RMVar_hsa_circ_120656,RMVar_hsa_circ_140063,RMVar_hsa_circ_140064,RMVar_hsa_circ_140066,RMVar_hsa_circ_98200,RMVar_hsa_circ_20507,RMVar_hsa_circ_140068,RMVar_hsa_circ_43424 86041 RMVar_ID_86041 Human_SNP_ID_51977805 m1A Human chr1 - 225920088 225920088 225920088 GCTGAAGCCCGAGGCAGGGTTGGTGTGATGCCAAGGCAAAGTGGTGAGGAGAAAACAGGAAACGG GCTGAAGCCCGAGGCAGGGTTGGTGTGATGCCGAGGCAAAGTGGTGAGGAGAAAACAGGAAACGG T C PYCR2,AL117348.2 Ensembl:ENSG00000143811,Ensembl:ENSG00000255835 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:225919976..225920225;chr1:225919988..225920250 26863196 MeRIP-seq:(Medium) rs956524234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803826,Human_RBP_ID_3937418,Human_RBP_ID_4028187,Human_RBP_ID_5136477,Human_RBP_ID_5312844,Human_RBP_ID_5768250,Human_RBP_ID_17740836,Human_RBP_ID_18157860,Human_RBP_ID_18429609,Human_RBP_ID_23368806,Human_RBP_ID_26386946 Human_miRNA_ID_137765,Human_miRNA_ID_414439,Human_miRNA_ID_593424,Human_miRNA_ID_2170786,Human_miRNA_ID_2216777 RMVar_hsa_circ_97459,RMVar_hsa_circ_125322,RMVar_hsa_circ_125649,RMVar_hsa_circ_104901,RMVar_hsa_circ_140071,RMVar_hsa_circ_76389,RMVar_hsa_circ_96375,RMVar_hsa_circ_140073,RMVar_hsa_circ_140074,RMVar_hsa_circ_140072,RMVar_hsa_circ_140069,RMVar_hsa_circ_140070 86042 RMVar_ID_86042 Human_SNP_ID_51977909 m1A Human chr1 - 225920485 225920482 225920485 ACCCCCTCCAGCCCAGGGAAGCTCCTCACAAGAAGCCTGGCCCTGGGAGGCAAGAAGGACTAAGG ACCCCCTCCAGCCCAGGGAAGCTCCTCACAAG___CCTGGCCCTGGGAGGCAAGAAGGACTAAGG GCTT G PYCR2,AL117348.2 Ensembl:ENSG00000143811,Ensembl:ENSG00000255835 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:225920434..225920567 26863196 MeRIP-seq:(Medium) rs908126155 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_343727,Human_RBP_ID_22426021 Human_miRNA_ID_2571989,Human_miRNA_ID_2661027,Human_miRNA_ID_2679482 RMVar_hsa_circ_97459,RMVar_hsa_circ_125322,RMVar_hsa_circ_125649,RMVar_hsa_circ_104901,RMVar_hsa_circ_140071,RMVar_hsa_circ_76389,RMVar_hsa_circ_96375,RMVar_hsa_circ_140073,RMVar_hsa_circ_140074,RMVar_hsa_circ_140072,RMVar_hsa_circ_140069,RMVar_hsa_circ_140070 86043 RMVar_ID_86043 Human_SNP_ID_51978254 m1A Human chr1 + 225921623 225921623 225921623 TGGCAAACCCATCTTCACCCCACCATCAGCCAATGCGTCCAGAGCCATGAATGCCTGTGGAGACA TGGCAAACCCATCTTCACCCCACCATCAGCCACTGCGTCCAGAGCCATGAATGCCTGTGGAGACA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225921572..225921648 26863196 MeRIP-seq:(Medium) rs1297872248 Functional Loss SNV dbSNP153 33..33 33 - - - 86044 RMVar_ID_86044 Human_SNP_ID_51978260 m1A Human chr1 - 225921638 225921638 225921638 CTGGGGCTTAGTGAGTGTCTCCACAGGCATTCATGGCTCTGGACGCATTGGCTGATGGTGGGGTG CTGGGGCTTAGTGAGTGTCTCCACAGGCATTCGTGGCTCTGGACGCATTGGCTGATGGTGGGGTG T C PYCR2,AL117348.2 Ensembl:ENSG00000143811,Ensembl:ENSG00000255835 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:225921588..225924229 32194978 MeRIP-seq:(Medium) rs370300338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_343731,Human_RBP_ID_4028221,Human_RBP_ID_5768262,Human_RBP_ID_8744088,Human_RBP_ID_8963941,Human_RBP_ID_10809714 Human_Splice_Rec_192948,Human_Splice_Rec_192949,Human_Splice_Rec_192962,Human_Splice_Rec_192963,Human_Splice_Rec_192970,Human_Splice_Rec_192971,Human_Splice_Rec_192980,Human_Splice_Rec_192981,Human_Splice_Rec_192986,Human_Splice_Rec_192987,Human_Splice_Rec_192992,Human_Splice_Rec_192996,Human_Splice_Rec_192997,Human_Splice_Rec_193006 Human_miRNA_ID_2823775,Human_miRNA_ID_2857746 RMVar_hsa_circ_97459,RMVar_hsa_circ_125322,RMVar_hsa_circ_104901,RMVar_hsa_circ_140071,RMVar_hsa_circ_96375,RMVar_hsa_circ_140072,RMVar_hsa_circ_140069,RMVar_hsa_circ_140070,RMVar_hsa_circ_32822,RMVar_hsa_circ_348234 86045 RMVar_ID_86045 Human_SNP_ID_51979111 m1A Human chr1 + 225924135 225924135 225924135 ACGCTCATGGTCCGCGGTTCACGCCTCCTGGGAGCCGCACGAACCCCCTCAGCGAGGGACCGGAA ACGCTCATGGTCCGCGGTTCACGCCTCCTGGGGGCCGCACGAACCCCCTCAGCGAGGGACCGGAA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:225924089..225924219 26863196 MeRIP-seq:(Medium) rs887101759 Functional Loss SNV dbSNP153 33..33 33 - - - 86046 RMVar_ID_86046 Human_SNP_ID_51979135 m1A Human chr1 + 225924176 225924176 225924176 AACCCCCTCAGCGAGGGACCGGAAGTAACGCTAGGGGAAGGGCGGACAGCGCAGGGGCGAACGGG AACCCCCTCAGCGAGGGACCGGAAGTAACGCTGGGGGAAGGGCGGACAGCGCAGGGGCGAACGGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:225924129..225924229 32194978 MeRIP-seq:(Medium) rs1277870049 Functional Loss SNV dbSNP153 33..33 33 - - - 86047 RMVar_ID_86047 Human_SNP_ID_51995919 m1A Human chr1 - 225987988 225987988 225987988 CTGGACTGAATAAGGATAAAGAGACAGAAGAAAGGACTGATGGGGAAAGAGTTGCTGAGGTAGCA CTGGACTGAATAAGGATAAAGAGACAGAAGAAGGGACTGATGGGGAAAGAGTTGCTGAGGTAGCA T C SDE2 Ensembl:ENSG00000143751 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:225987937..225988272 26863196 MeRIP-seq:(Medium) rs752211409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21539,Human_RBP_ID_343815,Human_RBP_ID_1422402,Human_RBP_ID_5768477,Human_RBP_ID_8744111,Human_RBP_ID_8963967,Human_RBP_ID_10810006,Human_RBP_ID_22431286,Human_RBP_ID_23368882,Human_RBP_ID_26312777,Human_RBP_ID_27176692,Human_RBP_ID_27799307 Human_Splice_Rec_193039 RMVar_hsa_circ_109300,RMVar_hsa_circ_140078,RMVar_hsa_circ_86403,RMVar_hsa_circ_140077,RMVar_hsa_circ_70142,RMVar_hsa_circ_284145,RMVar_hsa_circ_366699,RMVar_hsa_circ_361905,RMVar_hsa_circ_110340,RMVar_hsa_circ_140080,RMVar_hsa_circ_140081 86048 RMVar_ID_86048 Human_SNP_ID_51995941 m1A Human chr1 - 225988051 225988051 225988051 CAGAAGAGACCCAGGAGAAGAAGGCAGAGAGTAAAGAACCCATAGAAGAGGAGCCCACTGGGGCT CAGAAGAGACCCAGGAGAAGAAGGCAGAGAGTGAAGAACCCATAGAAGAGGAGCCCACTGGGGCT T C SDE2 Ensembl:ENSG00000143751 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:225987954..225988303 32194978 MeRIP-seq:(Medium) rs1382938692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21539,Human_RBP_ID_1422403,Human_RBP_ID_5768477,Human_RBP_ID_10810008,Human_RBP_ID_24541371,Human_RBP_ID_26312778,Human_RBP_ID_27799308 RMVar_hsa_circ_109300,RMVar_hsa_circ_140078,RMVar_hsa_circ_86403,RMVar_hsa_circ_140077,RMVar_hsa_circ_70142,RMVar_hsa_circ_284145,RMVar_hsa_circ_366699,RMVar_hsa_circ_361905,RMVar_hsa_circ_110340,RMVar_hsa_circ_140080,RMVar_hsa_circ_140081 86049 RMVar_ID_86049 Human_SNP_ID_51995957 m1A Human chr1 - 225988082 225988082 225988082 GAGCACATGGAAAGCAGGATGGTTACAGAAACAGAAGAGACCCAGGAGAAGAAGGCAGAGAGTAA GAGCACATGGAAAGCAGGATGGTTACAGAAACGGAAGAGACCCAGGAGAAGAAGGCAGAGAGTAA T C SDE2 Ensembl:ENSG00000143751 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:225987926..225988175 26863196 MeRIP-seq:(Medium) rs1051113051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21539,Human_RBP_ID_5768477,Human_RBP_ID_10810010,Human_RBP_ID_17646732,Human_RBP_ID_18564669,Human_RBP_ID_24647632,Human_RBP_ID_26315475,Human_RBP_ID_27799308 Human_miRNA_ID_2038533,Human_miRNA_ID_3017515 RMVar_hsa_circ_109300,RMVar_hsa_circ_140078,RMVar_hsa_circ_86403,RMVar_hsa_circ_140077,RMVar_hsa_circ_70142,RMVar_hsa_circ_284145,RMVar_hsa_circ_366699,RMVar_hsa_circ_361905,RMVar_hsa_circ_110340,RMVar_hsa_circ_140080,RMVar_hsa_circ_140081 86050 RMVar_ID_86050 Human_SNP_ID_51997988 m1A Human chr1 + 225995373 225995373 225995373 GTGCTCCATTGCATTTCACAAAGAAGTTTTCCACTGGAACATTCTAGAGACAAATTTGTTTTTTT GTGCTCCATTGCATTTCACAAAGAAGTTTTCCGCTGGAACATTCTAGAGACAAATTTGTTTTTTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:225995322..225999281 32194978 MeRIP-seq:(Medium) rs1405445679 Functional Loss SNV dbSNP153 33..33 33 - - - 86051 RMVar_ID_86051 Human_SNP_ID_52014570 m1A Human chr1 + 226062358 226062358 226062358 TTCCCCTCCCCCCACTTCCCTCCGGGCGCCCCAAACCCGGGCTTCGGGGGTTCGACGCCGTGCGC TTCCCCTCCCCCCACTTCCCTCCGGGCGCCCCTAACCCGGGCTTCGGGGGTTCGACGCCGTGCGC A T H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:226062355..226062534 26863196 MeRIP-seq:(Medium) rs1004505424 Functional Loss SNV dbSNP153 33..33 33 - - - 86052 RMVar_ID_86052 Human_SNP_ID_52014597 m1A Human chr1 - 226062439 226062439 226062439 GGCCGCCGGCTCCCGCCGAGACTGCCGCCCGCACCCGGCCAGCCCCCGCCCCCGGCCCTGCACTC GGCCGCCGGCTCCCGCCGAGACTGCCGCCCGCTCCCGGCCAGCCCCCGCCCCCGGCCCTGCACTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226062258..226062546 26863196 MeRIP-seq:(Medium) rs1411538451 Functional Loss SNV dbSNP153 33..33 33 - - - 86053 RMVar_ID_86053 Human_SNP_ID_52015018 m1A Human chr1 - 226063290 226063285 226063290 ACGGGGGAAAAAATATGGTCGGTGACCAGAGAAGAGAGACAAGATGGTGAAGCTTAGCAACAACT ACGGGGGAAAAAATATGGTCGGTGACCAGAGA_____GACAAGATGGTGAAGCTTAGCAACAACT CTCTCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:226063169..226063326 26863196 MeRIP-seq:(Medium) rs769910141 Functional Loss DEL dbSNP153 33..37 33 - - - 86054 RMVar_ID_86054 Human_SNP_ID_52015367 m1A Human chr1 + 226064272 226064271 226064272 TCCAGATTTGGGGAGGGGGTGATCGTGGCAGGAAAAGTTGTATGTTTGGTAGTTGCATATGGTGA TCCAGATTTGGGGAGGGGGTGATCGTGGCAGG_AAAGTTGTATGTTTGGTAGTTGCATATGGTGA GA G H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:226064261..226064346 26863410 MeRIP-seq:(Medium) rs1013101777 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_743964,Human_RBP_ID_855850 RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 86055 RMVar_ID_86055 Human_SNP_ID_52015368 m1A Human chr1 + 226064272 226064272 226064272 TCCAGATTTGGGGAGGGGGTGATCGTGGCAGGAAAAGTTGTATGTTTGGTAGTTGCATATGGTGA TCCAGATTTGGGGAGGGGGTGATCGTGGCAGGGAAAGTTGTATGTTTGGTAGTTGCATATGGTGA A G H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:226064261..226064346 26863410 MeRIP-seq:(Medium) rs567867002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743964,Human_RBP_ID_855850 RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 86056 RMVar_ID_86056 Human_SNP_ID_52015369 m1A Human chr1 + 226064272 226064272 226064272 TCCAGATTTGGGGAGGGGGTGATCGTGGCAGGAAAAGTTGTATGTTTGGTAGTTGCATATGGTGA TCCAGATTTGGGGAGGGGGTGATCGTGGCAGGTAAAGTTGTATGTTTGGTAGTTGCATATGGTGA A T H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:226064261..226064346 26863410 MeRIP-seq:(Medium) rs567867002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743964,Human_RBP_ID_855850 RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 86057 RMVar_ID_86057 Human_SNP_ID_52037189 m1A Human chr1 + 226146666 226146666 226146666 GTAGACTGATTTTGACCGCCACAAAGAGTAGGAGTTGTCAAACTTGAGGAGATAGACTCCTCTCC GTAGACTGATTTTGACCGCCACAAAGAGTAGGGGTTGTCAAACTTGAGGAGATAGACTCCTCTCC A G ACBD3-AS1 RNACentral:URS0000D5DED7 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226146616..226146766 32194978 MeRIP-seq:(Medium) rs113333885 Functional Loss SNV dbSNP153 33..33 33 - - - 86058 RMVar_ID_86058 Human_SNP_ID_52042087 m1A Human chr1 - 226165994 226165994 226165994 TTTCTTTGTGTTTCTTTTTCTTATAGAAAAAGATGGCAAAGCATTTCATCCAACTTATGAAGAAA TTTCTTTGTGTTTCTTTTTCTTATAGAAAAAGTTGGCAAAGCATTTCATCCAACTTATGAAGAAA T A ACBD3 Ensembl:ENSG00000182827 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226161616..226165993 32194978 MeRIP-seq:(Medium) rs962346460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745681,Human_RBP_ID_853241,Human_RBP_ID_27801607 Human_Splice_Rec_193116 RMVar_hsa_circ_331804,RMVar_hsa_circ_356670,RMVar_hsa_circ_360675,RMVar_hsa_circ_352941 86059 RMVar_ID_86059 Human_SNP_ID_52042088 m1A Human chr1 - 226165994 226165994 226165994 TTTCTTTGTGTTTCTTTTTCTTATAGAAAAAGATGGCAAAGCATTTCATCCAACTTATGAAGAAA TTTCTTTGTGTTTCTTTTTCTTATAGAAAAAGGTGGCAAAGCATTTCATCCAACTTATGAAGAAA T C ACBD3 Ensembl:ENSG00000182827 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226161616..226165993 32194978 MeRIP-seq:(Medium) rs962346460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745681,Human_RBP_ID_853241,Human_RBP_ID_27801607 Human_Splice_Rec_193116 RMVar_hsa_circ_331804,RMVar_hsa_circ_356670,RMVar_hsa_circ_360675,RMVar_hsa_circ_352941 86060 RMVar_ID_86060 Human_SNP_ID_52047755 m1A Human chr1 - 226186655 226186655 226186655 CAGCAGCCGGAGATGGCGGCGGTGCTGAACGCAGAGCGACTCGAGGTGTCCGTCGACGGCCTCAC CAGCAGCCGGAGATGGCGGCGGTGCTGAACGCTGAGCGACTCGAGGTGTCCGTCGACGGCCTCAC T A ACBD3 Ensembl:ENSG00000182827 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:226165943..226186750;chr1:226186357..226186730;chr1:226186526..226186750 26863196 MeRIP-seq:(Medium) rs77797743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1422500,Human_RBP_ID_4028521,Human_RBP_ID_8744171,Human_RBP_ID_9270671,Human_RBP_ID_9359907,Human_RBP_ID_22871069 86061 RMVar_ID_86061 Human_SNP_ID_52072632 m1A Human chr1 - 226289846 226289834 226289847 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCC_____________GGAGGACTACTTAGTTGTCCT CGGGGGGGGGGGTG C LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs869208548 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86062 RMVar_ID_86062 Human_SNP_ID_52072633 m1A Human chr1 - 226289846 226289834 226289847 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCC____________CGGAGGACTACTTAGTTGTCCT CGGGGGGGGGGGTG CG LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs869208548 Functional Loss DEL dbSNP153 32..43 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86063 RMVar_ID_86063 Human_SNP_ID_52072653 m1A Human chr1 - 226289846 226289835 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC___________CGGAGGACTACTTAGTTGTCCT GGGGGGGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1262303075 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86064 RMVar_ID_86064 Human_SNP_ID_52072657 m1A Human chr1 - 226289846 226289836 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC__________CCGGAGGACTACTTAGTTGTCCT GGGGGGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1359945063 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86065 RMVar_ID_86065 Human_SNP_ID_52072664 m1A Human chr1 - 226289846 226289837 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC_________CCCGGAGGACTACTTAGTTGTCCT GGGGGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1402098321 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86066 RMVar_ID_86066 Human_SNP_ID_52072672 m1A Human chr1 - 226289846 226289838 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC________CCCCGGAGGACTACTTAGTTGTCCT GGGGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1228935565 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86067 RMVar_ID_86067 Human_SNP_ID_52072686 m1A Human chr1 - 226289846 226289839 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC_______CCCCCGGAGGACTACTTAGTTGTCCT GGGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1461193178 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86068 RMVar_ID_86068 Human_SNP_ID_52072693 m1A Human chr1 - 226289846 226289840 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC______CCCCCCGGAGGACTACTTAGTTGTCCT GGGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1176359562 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86069 RMVar_ID_86069 Human_SNP_ID_52072703 m1A Human chr1 - 226289846 226289841 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC_____CCCCCCCGGAGGACTACTTAGTTGTCCT GGGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1306777284 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86070 RMVar_ID_86070 Human_SNP_ID_52072712 m1A Human chr1 - 226289846 226289842 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC____CCCCCCCCGGAGGACTACTTAGTTGTCCT GGGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1421462925 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86071 RMVar_ID_86071 Human_SNP_ID_52072718 m1A Human chr1 - 226289846 226289843 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC___CCCCCCCCCGGAGGACTACTTAGTTGTCCT GGGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1490231776 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86072 RMVar_ID_86072 Human_SNP_ID_52072724 m1A Human chr1 - 226289846 226289844 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC__CCCCCCCCCCGGAGGACTACTTAGTTGTCCT GGT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1237407322 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86073 RMVar_ID_86073 Human_SNP_ID_52072731 m1A Human chr1 - 226289846 226289845 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCC_CCCCCCCCCCCGGAGGACTACTTAGTTGTCCT GT G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs1302333029 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86074 RMVar_ID_86074 Human_SNP_ID_52072734 m1A Human chr1 - 226289846 226289846 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCCTCCCCCCCCCCCGGAGGACTACTTAGTTGTCCT T A LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs12046522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86075 RMVar_ID_86075 Human_SNP_ID_52072735 m1A Human chr1 - 226289846 226289846 226289846 AAAATTGCAACCTAGCTTTCCCACCCCCCCCCACCCCCCCCCCCGGAGGACTACTTAGTTGTCCT AAAATTGCAACCTAGCTTTCCCACCCCCCCCCCCCCCCCCCCCCGGAGGACTACTTAGTTGTCCT T G LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226289826..226289875 26863196 MeRIP-seq:(Medium) rs12046522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_140101,RMVar_hsa_circ_51172,RMVar_hsa_circ_332002,RMVar_hsa_circ_349357 86076 RMVar_ID_86076 Human_SNP_ID_52094253 m1A Human chr1 - 226374353 226374353 226374353 GGTCTCTTAGCAATGTGCTTTTTTCCTGAAGGATGAAGAGGCAGTGAAGAAGCTGACAGTAAATC GGTCTCTTAGCAATGTGCTTTTTTCCTGAAGGGTGAAGAGGCAGTGAAGAAGCTGACAGTAAATC T C PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226374304..226377157 32194978 MeRIP-seq:(Medium) rs1457348947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850903,Human_RBP_ID_18187871,Human_RBP_ID_22638145,Human_RBP_ID_22749803 Human_Splice_Rec_193280 86077 RMVar_ID_86077 Human_SNP_ID_52094968 m1A Human chr1 + 226377302 226377302 226377302 ACCCACACGGCCCCAGGACCTGAATATCCAATACCTGCAGTGGGAAGGAGGGTGTCAGATACACA ACCCACACGGCCCCAGGACCTGAATATCCAATGCCTGCAGTGGGAAGGAGGGTGTCAGATACACA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:226377206..226379144 26863410 MeRIP-seq:(Medium) rs751561930 Functional Loss SNV dbSNP153 33..33 33 - - - 86078 RMVar_ID_86078 Human_SNP_ID_52096582 m1A Human chr1 - 226383093 226383093 226383093 TCCCCCCAGAAACCAGCGCCTCCGTGGCGGCCACGCCTCCGCCCTCCACAGCCTCGGCTCCTGCT TCCCCCCAGAAACCAGCGCCTCCGTGGCGGCCCCGCCTCCGCCCTCCACAGCCTCGGCTCCTGCT T G PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226383002..226383141 26863196 MeRIP-seq:(Medium) rs1393949279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222359,Human_RBP_ID_4090047,Human_RBP_ID_8744232,Human_RBP_ID_9270689,Human_RBP_ID_9357614,Human_RBP_ID_22427843,Human_RBP_ID_22782480,Human_RBP_ID_24528825,Human_RBP_ID_26376362,Human_RBP_ID_26855024,Human_RBP_ID_27176803 Human_Splice_Rec_193268,Human_Splice_Rec_193269 RMVar_hsa_circ_118459,RMVar_hsa_circ_140108 86079 RMVar_ID_86079 Human_SNP_ID_52098013 m1A Human chr1 + 226388726 226388726 226388726 CTTTTTTAGATTTCTTCTTCGCCACTTCATCCACTCCATCCACCTCATCGCCTTTTCTCTTTCTG CTTTTTTAGATTTCTTCTTCGCCACTTCATCCGCTCCATCCACCTCATCGCCTTTTCTCTTTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:226388676..226388775;chr1:226388676..226388819 26863196 MeRIP-seq:(Medium) rs144925873 Functional Loss SNV dbSNP153 33..33 33 - - - 86080 RMVar_ID_86080 Human_SNP_ID_52098410 m1A Human chr1 - 226390357 226390357 226390357 TTGCCCTGGGGGTTCAGTGAGGGGTTCAAGGGAGGCCCAAAGGCCCTACAGGTTCCATACCACTC TTGCCCTGGGGGTTCAGTGAGGGGTTCAAGGGGGGCCCAAAGGCCCTACAGGTTCCATACCACTC T C PARP1 Ensembl:ENSG00000143799 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:226390355..226390475 26863196 MeRIP-seq:(Medium) rs1443861629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22350973 RMVar_hsa_circ_118459,RMVar_hsa_circ_140108,RMVar_hsa_circ_59216 86081 RMVar_ID_86081 Human_SNP_ID_52098450 m1A Human chr1 - 226390462 226390462 226390462 CGAGTCAGCTCAAGGGCTTCAGCCTCCTTGCTACAGAGGATAAAGAAGCCCTGAAGAAGCAGCTC CGAGTCAGCTCAAGGGCTTCAGCCTCCTTGCTGCAGAGGATAAAGAAGCCCTGAAGAAGCAGCTC T C PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226390401..226392677 32194978 MeRIP-seq:(Medium) rs143482147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344032,Human_RBP_ID_975482,Human_RBP_ID_1738810,Human_RBP_ID_2127431,Human_RBP_ID_4090065,Human_RBP_ID_5769715,Human_RBP_ID_8300590,Human_RBP_ID_8744245,Human_RBP_ID_9253184,Human_RBP_ID_9271811,Human_RBP_ID_9357621,Human_RBP_ID_17741099,Human_RBP_ID_18564864,Human_RBP_ID_22018645,Human_RBP_ID_22782488,Human_RBP_ID_26312816,Human_RBP_ID_26855041 Human_Splice_Rec_193261,Human_Splice_Rec_193335 Human_miRNA_ID_2352656 RMVar_hsa_circ_118459,RMVar_hsa_circ_140108,RMVar_hsa_circ_59216 86082 RMVar_ID_86082 Human_SNP_ID_52098507 m1A Human chr1 - 226390602 226390602 226390602 TTTCCTGCAGGGCCAGGTGCGCCTGTCCAAGAAGATGGTGGACCCGGAGAAGCCACAGCTAGGCA TTTCCTGCAGGGCCAGGTGCGCCTGTCCAAGATGATGGTGGACCCGGAGAAGCCACAGCTAGGCA T A PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:226390551..226390625 26863196 MeRIP-seq:(Medium) rs749501376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222363,Human_RBP_ID_850907,Human_RBP_ID_1738813,Human_RBP_ID_4028749,Human_RBP_ID_5338935,Human_RBP_ID_5769719,Human_RBP_ID_8754411,Human_RBP_ID_9253185,Human_RBP_ID_9270695,Human_RBP_ID_9357623,Human_RBP_ID_17741101,Human_RBP_ID_24541868,Human_RBP_ID_26312818 Human_Splice_Rec_193260,Human_Splice_Rec_193334 RMVar_hsa_circ_118459,RMVar_hsa_circ_140108,RMVar_hsa_circ_59216 86083 RMVar_ID_86083 Human_SNP_ID_52098906 m1A Human chr1 - 226392180 226392180 226392180 AGAAGATAGAAAAGGTAAGATCTTGGGGGCCCAGATCCCTGAACTTTATGGATTGCTTGCAATGA AGAAGATAGAAAAGGTAAGATCTTGGGGGCCCGGATCCCTGAACTTTATGGATTGCTTGCAATGA T C PARP1 Ensembl:ENSG00000143799 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:226392176..226392225 26863196 MeRIP-seq:(Medium) rs762568850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118459,RMVar_hsa_circ_140108,RMVar_hsa_circ_59216 86084 RMVar_ID_86084 Human_SNP_ID_52098941 m1A Human chr1 + 226392262 226392262 226392262 GTACTTCTGTTGGACTTGGCATACTCTGCTGCAAAGTCACCCAGAGTCTTCTCTGCCTTGCTACC GTACTTCTGTTGGACTTGGCATACTCTGCTGCGAAGTCACCCAGAGTCTTCTCTGCCTTGCTACC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:226392176..226392363 26863410 MeRIP-seq:(Medium) rs61750986 Functional Loss SNV dbSNP153 33..33 33 - - - 86085 RMVar_ID_86085 Human_SNP_ID_52101520 m1A Human chr1 - 226402168 226402168 226402168 GGGGCAGCATGGGCATTCAGCCCCCACCCTGAAGCTCCCAGGAGGGCCTCGTCTCAGAGAGCAAA GGGGCAGCATGGGCATTCAGCCCCCACCCTGAGGCTCCCAGGAGGGCCTCGTCTCAGAGAGCAAA T C PARP1 Ensembl:ENSG00000143799 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226402164..226402326 26863196 MeRIP-seq:(Medium) rs768937503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19044505,Human_RBP_ID_22352015 86086 RMVar_ID_86086 Human_SNP_ID_52103105 m1A Human chr1 + 226407981 226407981 226407981 AAGCTCCGGAAGCCCGACGCCACGACCTAGAAACACGCTGCCGCCTCGCCGCCTCGCGTGCGCTC AAGCTCCGGAAGCCCGACGCCACGACCTAGAACCACGCTGCCGCCTCGCCGCCTCGCGTGCGCTC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:226407893..226408100 26863196 MeRIP-seq:(Medium) rs770686693 Functional Loss SNV dbSNP153 33..33 33 - - - 86087 RMVar_ID_86087 Human_SNP_ID_52103114 m1A Human chr1 - 226408012 226408012 226408012 GCTCTGGCCGCTCAGGCGCCTGCGGCTGGGTGAGCGCACGCGAGGCGGCGAGGCGGCAGCGTGTT GCTCTGGCCGCTCAGGCGCCTGCGGCTGGGTGGGCGCACGCGAGGCGGCGAGGCGGCAGCGTGTT T C PARP1 Ensembl:ENSG00000143799 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:226407826..226408100 26863410 MeRIP-seq:(Medium) rs1016012009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25228,Human_RBP_ID_344052,Human_RBP_ID_4028765,Human_RBP_ID_8754421,Human_RBP_ID_9270699,Human_RBP_ID_9320378,Human_RBP_ID_9357630,Human_RBP_ID_18564892,Human_RBP_ID_22735522,Human_RBP_ID_26855063 86088 RMVar_ID_86088 Human_SNP_ID_52103129 m1A Human chr1 + 226408054 226408054 226408054 GCAGGCGCCTGAGCGGCCAGAGCCGCCACCGAACACGCCGCACCGGCCACCGCCGTTCCCTGATA GCAGGCGCCTGAGCGGCCAGAGCCGCCACCGATCACGCCGCACCGGCCACCGCCGTTCCCTGATA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:226407876..226408100 26863196 MeRIP-seq:(Medium) rs1342071910 Functional Loss SNV dbSNP153 33..33 33 - - - 86089 RMVar_ID_86089 Human_SNP_ID_52181802 m1A Human chr1 - 226736318 226736318 226736318 GGAAGATGGGGAAAGGATATCTGCCCTGTGGCATGCCGGGCTCTGGGGAGCCTGAAGTGGGCAAA GGAAGATGGGGAAAGGATATCTGCCCTGTGGCCTGCCGGGCTCTGGGGAGCCTGAAGTGGGCAAA T G ITPKB Ensembl:ENSG00000143772 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:226736268..226736470 26863196 MeRIP-seq:(Medium) rs753362652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8744287,Human_RBP_ID_9267921 Human_miRNA_ID_2256168,Human_miRNA_ID_2576976 RMVar_hsa_circ_99743,RMVar_hsa_circ_140109,RMVar_hsa_circ_83555,RMVar_hsa_circ_140111 86090 RMVar_ID_86090 Human_SNP_ID_52181804 m1A Human chr1 + 226736324 226736324 226736324 CACTTCAGGCTCCCCAGAGCCCGGCATGCCACAGGGCAGATATCCTTTCCCCATCTTCCCAGGGG CACTTCAGGCTCCCCAGAGCCCGGCATGCCACCGGGCAGATATCCTTTCCCCATCTTCCCAGGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:226736275..226736499;chr1:226736273..226736473 26863196 MeRIP-seq:(Medium) rs936873356 Functional Loss SNV dbSNP153 33..33 33 - - - 86091 RMVar_ID_86091 Human_SNP_ID_52181805 m1A Human chr1 + 226736324 226736324 226736324 CACTTCAGGCTCCCCAGAGCCCGGCATGCCACAGGGCAGATATCCTTTCCCCATCTTCCCAGGGG CACTTCAGGCTCCCCAGAGCCCGGCATGCCACGGGGCAGATATCCTTTCCCCATCTTCCCAGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:226736275..226736499;chr1:226736273..226736473 26863196 MeRIP-seq:(Medium) rs936873356 Functional Loss SNV dbSNP153 33..33 33 - - - 86092 RMVar_ID_86092 Human_SNP_ID_52181931 m1A Human chr1 + 226736573 226736573 226736573 CACTTCCGTGGCCATCGTTAAGCTAGCTCCGAACAGCCCCAATGAGGGAGCTAGGCAGCTCCGAG CACTTCCGTGGCCATCGTTAAGCTAGCTCCGAGCAGCCCCAATGAGGGAGCTAGGCAGCTCCGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226736525..226736638 32194978 MeRIP-seq:(Medium) rs1483907427 Functional Loss SNV dbSNP153 33..33 33 - - - 86093 RMVar_ID_86093 Human_SNP_ID_52182331 m1A Human chr1 + 226737287 226737287 226737287 CTCCTCGGGGGACAGCGACTCGGCTGGGGGGAAGAGGAAAGAGGCGCCTCTCCCGGGGCTGAAAA CTCCTCGGGGGACAGCGACTCGGCTGGGGGGAGGAGGAAAGAGGCGCCTCTCCCGGGGCTGAAAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:226737243..226737398 26863196 MeRIP-seq:(Medium) rs1366143053 Functional Loss SNV dbSNP153 33..33 33 - - - 86094 RMVar_ID_86094 Human_SNP_ID_52183007 m1A Human chr1 - 226739156 226739156 226739156 CCTCTTTCGCACTCCTCTTTTTTGTCTTCCATAGCTTGTGAGAAAATAATTTCTGAGCATTTTTA CCTCTTTCGCACTCCTCTTTTTTGTCTTCCATTGCTTGTGAGAAAATAATTTCTGAGCATTTTTA T A ITPKB Ensembl:ENSG00000143772 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:226739112..226739404 26863196 MeRIP-seq:(Medium) rs1187285518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2778895,Human_miRNA_ID_3119712 RMVar_hsa_circ_99743,RMVar_hsa_circ_140109 86095 RMVar_ID_86095 Human_SNP_ID_52183018 m1A Human chr1 + 226739184 226739183 226739185 AAGCTATGGAAGACAAAAAAGAGGAGTGCGAAAGAGGGGGGAAAGCTCTTCGGTTCAGGGGCCCG AAGCTATGGAAGACAAAAAAGAGGAGTGCGAA__AGGGGGGAAAGCTCTTCGGTTCAGGGGCCCG AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:226739138..226739247 26863196 MeRIP-seq:(Medium) rs1292345901 Functional Loss DEL dbSNP153 33..34 33 - - - 86096 RMVar_ID_86096 Human_SNP_ID_52183044 m1A Human chr1 + 226739228 226739228 226739228 GCTCTTCGGTTCAGGGGCCCGGCGATCCCGGCAGTGGCGACGCCAAGCCGGCCCTGCACGCCCTT GCTCTTCGGTTCAGGGGCCCGGCGATCCCGGCGGTGGCGACGCCAAGCCGGCCCTGCACGCCCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:226739008..226739299 26863196 MeRIP-seq:(Medium) rs1333885628 Functional Loss SNV dbSNP153 33..33 33 - - - 86097 RMVar_ID_86097 Human_SNP_ID_52213392 m1A Human chr1 + 226870643 226870643 226870643 CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCAGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCGGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC A G PSEN2 Ensembl:ENSG00000143801 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12758915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_193405,Human_Splice_Rec_193413,Human_Splice_Rec_193437 Human_miRNA_ID_2394315,Human_miRNA_ID_2906249,Human_miRNA_ID_3025079 Clinvar_Rec_453,Clinvar_Rec_454,Clinvar_Rec_455,Clinvar_Rec_456 GWAS_ID_10209,GWAS_ID_10210,GWAS_ID_10211,GWAS_ID_10212,GWAS_ID_10213,GWAS_ID_10214,GWAS_ID_10215,GWAS_ID_10216,GWAS_ID_10217,GWAS_ID_10218,GWAS_ID_10219,GWAS_ID_10220,GWAS_ID_10221,GWAS_ID_10222,GWAS_ID_10223,GWAS_ID_10224,GWAS_ID_10225,GWAS_ID_10226,GWAS_ID_10227,GWAS_ID_10228,GWAS_ID_10229,GWAS_ID_10230,GWAS_ID_10231,GWAS_ID_10232,GWAS_ID_10233,GWAS_ID_10234,GWAS_ID_10235,GWAS_ID_10236,GWAS_ID_10237,GWAS_ID_10238,GWAS_ID_10239,GWAS_ID_10240,GWAS_ID_10241,GWAS_ID_10242,GWAS_ID_10243,GWAS_ID_10244,GWAS_ID_10245,GWAS_ID_10246,GWAS_ID_10247,GWAS_ID_10248,GWAS_ID_10249,GWAS_ID_10250,GWAS_ID_10251,GWAS_ID_10252,GWAS_ID_10253,GWAS_ID_10254,GWAS_ID_10255,GWAS_ID_10256,GWAS_ID_10257,GWAS_ID_10258,GWAS_ID_10259,GWAS_ID_10260,GWAS_ID_10261,GWAS_ID_10262,GWAS_ID_10263,GWAS_ID_10264,GWAS_ID_10265,GWAS_ID_10266,GWAS_ID_10267,GWAS_ID_10268,GWAS_ID_10269,GWAS_ID_10270,GWAS_ID_10271,GWAS_ID_10272,GWAS_ID_10273,GWAS_ID_10274,GWAS_ID_10275,GWAS_ID_10276,GWAS_ID_10277,GWAS_ID_10278,GWAS_ID_10279,GWAS_ID_10280,GWAS_ID_10281,GWAS_ID_10282,GWAS_ID_10283,GWAS_ID_10284,GWAS_ID_10285,GWAS_ID_10286,GWAS_ID_10287,GWAS_ID_10288,GWAS_ID_10289 RMVar_hsa_circ_77887,RMVar_hsa_circ_140112 86098 RMVar_ID_86098 Human_SNP_ID_52213393 m1A Human chr1 + 226870643 226870643 226870643 CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCAGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCTGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC A T PSEN2 Ensembl:ENSG00000143801 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12758915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_193405,Human_Splice_Rec_193413,Human_Splice_Rec_193437 Human_miRNA_ID_2394315,Human_miRNA_ID_2906249,Human_miRNA_ID_3025079 Clinvar_Rec_453,Clinvar_Rec_454,Clinvar_Rec_455,Clinvar_Rec_456 GWAS_ID_10209,GWAS_ID_10210,GWAS_ID_10211,GWAS_ID_10212,GWAS_ID_10213,GWAS_ID_10214,GWAS_ID_10215,GWAS_ID_10216,GWAS_ID_10217,GWAS_ID_10218,GWAS_ID_10219,GWAS_ID_10220,GWAS_ID_10221,GWAS_ID_10222,GWAS_ID_10223,GWAS_ID_10224,GWAS_ID_10225,GWAS_ID_10226,GWAS_ID_10227,GWAS_ID_10228,GWAS_ID_10229,GWAS_ID_10230,GWAS_ID_10231,GWAS_ID_10232,GWAS_ID_10233,GWAS_ID_10234,GWAS_ID_10235,GWAS_ID_10236,GWAS_ID_10237,GWAS_ID_10238,GWAS_ID_10239,GWAS_ID_10240,GWAS_ID_10241,GWAS_ID_10242,GWAS_ID_10243,GWAS_ID_10244,GWAS_ID_10245,GWAS_ID_10246,GWAS_ID_10247,GWAS_ID_10248,GWAS_ID_10249,GWAS_ID_10250,GWAS_ID_10251,GWAS_ID_10252,GWAS_ID_10253,GWAS_ID_10254,GWAS_ID_10255,GWAS_ID_10256,GWAS_ID_10257,GWAS_ID_10258,GWAS_ID_10259,GWAS_ID_10260,GWAS_ID_10261,GWAS_ID_10262,GWAS_ID_10263,GWAS_ID_10264,GWAS_ID_10265,GWAS_ID_10266,GWAS_ID_10267,GWAS_ID_10268,GWAS_ID_10269,GWAS_ID_10270,GWAS_ID_10271,GWAS_ID_10272,GWAS_ID_10273,GWAS_ID_10274,GWAS_ID_10275,GWAS_ID_10276,GWAS_ID_10277,GWAS_ID_10278,GWAS_ID_10279,GWAS_ID_10280,GWAS_ID_10281,GWAS_ID_10282,GWAS_ID_10283,GWAS_ID_10284,GWAS_ID_10285,GWAS_ID_10286,GWAS_ID_10287,GWAS_ID_10288,GWAS_ID_10289 RMVar_hsa_circ_77887,RMVar_hsa_circ_140112 86099 RMVar_ID_86099 Human_SNP_ID_52216379 m1A Human chr1 + 226881986 226881986 226881986 AGCGGACGTCCCTAATGTCGGCTGAGAGCCCCACGCCGCGCTCCTGCCAGGAGGGCAGGCAGGGC AGCGGACGTCCCTAATGTCGGCTGAGAGCCCCGCGCCGCGCTCCTGCCAGGAGGGCAGGCAGGGC A G PSEN2 Ensembl:ENSG00000143801 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:226881937..226882094 26863196 MeRIP-seq:(Medium) rs147326133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_193404,Human_Splice_Rec_193408,Human_Splice_Rec_193409,Human_Splice_Rec_193418,Human_Splice_Rec_193419,Human_Splice_Rec_193442,Human_Splice_Rec_193443,Human_Splice_Rec_193478,Human_Splice_Rec_193479,Human_Splice_Rec_193498,Human_Splice_Rec_193499 RMVar_hsa_circ_77887,RMVar_hsa_circ_127584,RMVar_hsa_circ_140112,RMVar_hsa_circ_118553,RMVar_hsa_circ_140113,RMVar_hsa_circ_34241,RMVar_hsa_circ_140114 86100 RMVar_ID_86100 Human_SNP_ID_52216888 m1A Human chr1 + 226883828 226883828 226883828 AGCTGACCCTCAAATACGGAGCGAAGCACGTGATCATGCTGTTTGTGCCTGTCACTCTGTGCATG AGCTGACCCTCAAATACGGAGCGAAGCACGTGTTCATGCTGTTTGTGCCTGTCACTCTGTGCATG A T PSEN2 Ensembl:ENSG00000143801 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226883777..226883876 32194978 MeRIP-seq:(Medium) rs1222893058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_193411,Human_Splice_Rec_193421,Human_Splice_Rec_193445,Human_Splice_Rec_193481,Human_Splice_Rec_193501 RMVar_hsa_circ_77887,RMVar_hsa_circ_127584,RMVar_hsa_circ_140112,RMVar_hsa_circ_75766,RMVar_hsa_circ_118553,RMVar_hsa_circ_140113,RMVar_hsa_circ_34241,RMVar_hsa_circ_140114,RMVar_hsa_circ_140115 86101 RMVar_ID_86101 Human_SNP_ID_52217263 m1A Human chr1 + 226885016 226885016 226885016 GCGCAGAACAGGTGAAAGCATGGAGAGAATGCAGCCAGCGGTTTGTTTGCAGCAGTCCAGGCTGG GCGCAGAACAGGTGAAAGCATGGAGAGAATGCGGCCAGCGGTTTGTTTGCAGCAGTCCAGGCTGG A G PSEN2 Ensembl:ENSG00000143801 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:226885014..226885099 26863196 MeRIP-seq:(Medium) rs1377050604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77887,RMVar_hsa_circ_127584,RMVar_hsa_circ_140112,RMVar_hsa_circ_75766,RMVar_hsa_circ_118553,RMVar_hsa_circ_140113,RMVar_hsa_circ_140114,RMVar_hsa_circ_140115 86102 RMVar_ID_86102 Human_SNP_ID_52220146 m1A Human chr1 - 226895440 226895440 226895440 GCAGCGCCTTCTTGAACACAGCAAGCAGCAGGAGGGTCAGACACAAGCCCTGCAGGACATGGAGG GCAGCGCCTTCTTGAACACAGCAAGCAGCAGGTGGGTCAGACACAAGCCCTGCAGGACATGGAGG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226891805..226895858 32194978 MeRIP-seq:(Medium) rs770838733 Functional Loss SNV dbSNP153 33..33 33 - - - 86103 RMVar_ID_86103 Human_SNP_ID_52230640 m1A Human chr1 + 226940356 226940356 226940356 GCGCGGTGGCCAGCGCGCAGAGGCGGGCGCGGAGGCGGCTAGAAGGTGACCGCGGATCCCAGCTT GCGCGGTGGCCAGCGCGCAGAGGCGGGCGCGGGGGCGGCTAGAAGGTGACCGCGGATCCCAGCTT A G COQ8A Ensembl:ENSG00000163050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:226940243..226940488 26863196 MeRIP-seq:(Medium) rs938134997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4076418,Human_RBP_ID_18415883,Human_RBP_ID_22428819 Human_Splice_Rec_193585,Human_Splice_Rec_193613,Human_Splice_Rec_193627 RMVar_hsa_circ_99597,RMVar_hsa_circ_140123 86104 RMVar_ID_86104 Human_SNP_ID_52237234 m1A Human chr1 + 226965095 226965095 226965095 TTCTCAGTCCCGCATGCAGCCGGAGCCTCCACAGACTTCTCTTCAGCCTCCGCTCCCGACCAGTC TTCTCAGTCCCGCATGCAGCCGGAGCCTCCACGGACTTCTCTTCAGCCTCCGCTCCCGACCAGTC A G COQ8A Ensembl:ENSG00000163050 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226965045..226965207 26863196 MeRIP-seq:(Medium) rs1314751036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_975495,Human_RBP_ID_3934593,Human_RBP_ID_4028942,Human_RBP_ID_8744300,Human_RBP_ID_18564931 Human_Splice_Rec_193558,Human_Splice_Rec_193588,Human_Splice_Rec_193630,Human_Splice_Rec_193658 Human_miRNA_ID_2712441,Human_miRNA_ID_3048424 RMVar_hsa_circ_21257,RMVar_hsa_circ_99597,RMVar_hsa_circ_281105,RMVar_hsa_circ_140123,RMVar_hsa_circ_344409,RMVar_hsa_circ_140124 86105 RMVar_ID_86105 Human_SNP_ID_52242176 m1A Human chr1 + 226982078 226982078 226982078 TTCCAGTCCTTTCCTGTCCGAGGCCAATGCAGAGCGGATCGTGCGCACGCTCTGCAAGGTGCGTG TTCCAGTCCTTTCCTGTCCGAGGCCAATGCAGGGCGGATCGTGCGCACGCTCTGCAAGGTGCGTG A G COQ8A Ensembl:ENSG00000163050 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:226982016..226982179 26863196 MeRIP-seq:(Medium) rs771143366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855868,Human_RBP_ID_9270704,Human_RBP_ID_18966460 Human_Splice_Rec_193564,Human_Splice_Rec_193565,Human_Splice_Rec_193594,Human_Splice_Rec_193595,Human_Splice_Rec_193616,Human_Splice_Rec_193636,Human_Splice_Rec_193637,Human_Splice_Rec_193666,Human_Splice_Rec_193667 RMVar_hsa_circ_99597,RMVar_hsa_circ_140123 86106 RMVar_ID_86106 Human_SNP_ID_52242179 m1A Human chr1 + 226982083 226982083 226982083 GTCCTTTCCTGTCCGAGGCCAATGCAGAGCGGATCGTGCGCACGCTCTGCAAGGTGCGTGGTGCG GTCCTTTCCTGTCCGAGGCCAATGCAGAGCGGTTCGTGCGCACGCTCTGCAAGGTGCGTGGTGCG A T COQ8A Ensembl:ENSG00000163050 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226977503..226982261 26863196 MeRIP-seq:(Medium) rs769965625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855868,Human_RBP_ID_9270704,Human_RBP_ID_18966460 Human_Splice_Rec_193564,Human_Splice_Rec_193565,Human_Splice_Rec_193594,Human_Splice_Rec_193595,Human_Splice_Rec_193616,Human_Splice_Rec_193636,Human_Splice_Rec_193637,Human_Splice_Rec_193666,Human_Splice_Rec_193667 RMVar_hsa_circ_99597,RMVar_hsa_circ_140123 86107 RMVar_ID_86107 Human_SNP_ID_52242423 m1A Human chr1 - 226982759 226982759 226982759 AGAGTGGGCAGAGCCCCTGGCTCCTCACCATCATCTGCTTCAGTGGCATGAAGTCCGCGCTCTGC AGAGTGGGCAGAGCCCCTGGCTCCTCACCATCGTCTGCTTCAGTGGCATGAAGTCCGCGCTCTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226982709..226983040 32194978 MeRIP-seq:(Medium) rs776413284 Functional Loss SNV dbSNP153 33..33 33 - - - 86108 RMVar_ID_86108 Human_SNP_ID_52242870 m1A Human chr1 - 226983814 226983812 226983814 GCGGGCACAGGCGGCCTCTCGCTGGTAGTCACACTCCAGGGCCAGCTCCCGCCTCAGCACGTCGA GCGGGCACAGGCGGCCTCTCGCTGGTAGTCAC__TCCAGGGCCAGCTCCCGCCTCAGCACGTCGA AGT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226983639..226983890 32194978 MeRIP-seq:(Medium) rs1453487075 Functional Loss DEL dbSNP153 33..34 33 - - - 86109 RMVar_ID_86109 Human_SNP_ID_52242872 m1A Human chr1 - 226983814 226983814 226983814 GCGGGCACAGGCGGCCTCTCGCTGGTAGTCACACTCCAGGGCCAGCTCCCGCCTCAGCACGTCGA GCGGGCACAGGCGGCCTCTCGCTGGTAGTCACGCTCCAGGGCCAGCTCCCGCCTCAGCACGTCGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226983639..226983890 32194978 MeRIP-seq:(Medium) rs760238739 Functional Loss SNV dbSNP153 33..33 33 - - - 86110 RMVar_ID_86110 Human_SNP_ID_52244094 m1A Human chr1 + 226986550 226986550 226986550 TTTTGATTTTGGCACTCAGAGCACCACCGAGAAGATCCACAACCTGATTCCCGTCATGCTGAGGC TTTTGATTTTGGCACTCAGAGCACCACCGAGAGGATCCACAACCTGATTCCCGTCATGCTGAGGC A G COQ8A Ensembl:ENSG00000163050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:226984601..226986595 32194978 MeRIP-seq:(Medium) rs113308613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1738843,Human_RBP_ID_3934599,Human_RBP_ID_10815264,Human_RBP_ID_17450433,Human_RBP_ID_22024301 Human_Splice_Rec_193582,Human_Splice_Rec_193612,Human_Splice_Rec_193626,Human_Splice_Rec_193654,Human_Splice_Rec_193684,Human_Splice_Rec_193696 RMVar_hsa_circ_140125,RMVar_hsa_circ_118585 86111 RMVar_ID_86111 Human_SNP_ID_52303644 m1A Human chr1 + 227220524 227220524 227220524 ATTAATTCTATCACTCTCAACAGAACTTTACTAATCTTCCAAAATGTCCTGTGCCACCCTGCCAC ATTAATTCTATCACTCTCAACAGAACTTTACTCATCTTCCAAAATGTCCTGTGCCACCCTGCCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227220520..227220735 26863196 MeRIP-seq:(Medium) rs1324680694 Functional Loss SNV dbSNP153 33..33 33 - - - 86112 RMVar_ID_86112 Human_SNP_ID_52303645 m1A Human chr1 + 227220524 227220524 227220524 ATTAATTCTATCACTCTCAACAGAACTTTACTAATCTTCCAAAATGTCCTGTGCCACCCTGCCAC ATTAATTCTATCACTCTCAACAGAACTTTACTGATCTTCCAAAATGTCCTGTGCCACCCTGCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227220520..227220735 26863196 MeRIP-seq:(Medium) rs1324680694 Functional Loss SNV dbSNP153 33..33 33 - - - 86113 RMVar_ID_86113 Human_SNP_ID_52329043 m1A Human chr1 - 227318354 227318354 227318354 GGGCTGGAAGGGAGAGGAAGGGAGTGGTTGGGAGCCGGGCTGCCGCAGCCTCTAGTCTCCTCAGC GGGCTGGAAGGGAGAGGAAGGGAGTGGTTGGGCGCCGGGCTGCCGCAGCCTCTAGTCTCCTCAGC T G CDC42BPA Ensembl:ENSG00000143776 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227318200..227318502 26863196 MeRIP-seq:(Medium) rs1327479448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073302,Human_RBP_ID_5158722,Human_RBP_ID_5311999,Human_RBP_ID_5485562,Human_RBP_ID_5519995,Human_RBP_ID_18415146,Human_RBP_ID_22024312,Human_RBP_ID_26855265 86114 RMVar_ID_86114 Human_SNP_ID_52351675 m1A Human chr1 - 227410914 227410914 227410914 CAGCAGCAATGAAGATTTCCTGATGGAAGATGATGACAATAGTGACTATGGCAATTCAAAAAAGA CAGCAGCAATGAAGATTTCCTGATGGAAGATGTTGACAATAGTGACTATGGCAATTCAAAAAAGA T A NUCKS1P1 Ensembl:ENSG00000232864 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227410895..227410960 26863196 MeRIP-seq:(Medium) rs949958532 Functional Loss SNV dbSNP153 33..33 33 - - - 86115 RMVar_ID_86115 Human_SNP_ID_52356310 m1A Human chr1 + 227431021 227431021 227431021 GGCCTTGTCTGTTAATAAATAGTTTATATACCAAAAAAAAAAAAAAATGCAGAGATAGTGTGGGA GGCCTTGTCTGTTAATAAATAGTTTATATACCCAAAAAAAAAAAAAATGCAGAGATAGTGTGGGA A C LINC01641 Ensembl:ENSG00000234277 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1245741140 Functional Loss SNV dbSNP153 33..33 33 - - - 86116 RMVar_ID_86116 Human_SNP_ID_52404452 m1A Human chr1 + 227638674 227638674 227638674 CCACAGGGGTCTAGGTGGATGTCTTGGGTACTATGGGAAATGTGGAAGTAGGGAGTAATGTGGAG CCACAGGGGTCTAGGTGGATGTCTTGGGTACTGTGGGAAATGTGGAAGTAGGGAGTAATGTGGAG A G ZNF678 Ensembl:ENSG00000181450 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227638624..227638841 26863196 MeRIP-seq:(Medium) rs1048638346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140201 86117 RMVar_ID_86117 Human_SNP_ID_52426953 m1A Human chr1 + 227732531 227732531 227732531 CCAAGGAGGCCAGCACCTCTGTGATGCGCCCAACATCAAAGGCTGCCTGTTCGAAACCCAACCCA CCAAGGAGGCCAGCACCTCTGTGATGCGCCCACCATCAAAGGCTGCCTGTTCGAAACCCAACCCA A C SNAP47 Ensembl:ENSG00000143740 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227732480..227732650 26863196 MeRIP-seq:(Medium) rs780847189 Functional Loss SNV dbSNP153 33..33 33 - - - 86118 RMVar_ID_86118 Human_SNP_ID_52426954 m1A Human chr1 + 227732531 227732531 227732531 CCAAGGAGGCCAGCACCTCTGTGATGCGCCCAACATCAAAGGCTGCCTGTTCGAAACCCAACCCA CCAAGGAGGCCAGCACCTCTGTGATGCGCCCAGCATCAAAGGCTGCCTGTTCGAAACCCAACCCA A G SNAP47 Ensembl:ENSG00000143740 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227732480..227732650 26863196 MeRIP-seq:(Medium) rs780847189 Functional Loss SNV dbSNP153 33..33 33 - - - 86119 RMVar_ID_86119 Human_SNP_ID_52427861 m1A Human chr1 - 227734862 227734862 227734862 CTGGAGAGTTCCTCTGCAGACGGTTTGGAGTGAGGACGGGGCCCAGGGAGATGGCATGGACCGTG CTGGAGAGTTCCTCTGCAGACGGTTTGGAGTGCGGACGGGGCCCAGGGAGATGGCATGGACCGTG T G JMJD4 Ensembl:ENSG00000081692 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:227734855..227734939 26863196 MeRIP-seq:(Medium) rs1558184186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5336268,Human_RBP_ID_10821466,Human_RBP_ID_22535693,Human_RBP_ID_22635841 86120 RMVar_ID_86120 Human_SNP_ID_52427990 m1A Human chr1 + 227735185 227735163 227735185 AGGAGAAGGCGCCCGGCTCCGAGACGAAGGCTACCCGGCCCGGAGCCTGGCCGACGCCGGGGACA AGGAGAAGGCG______________________CCCGGCCCGGAGCCTGGCCGACGCCGGGGACA GCCCGGCTCCGAGACGAAGGCTA G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227735144..227735241 26863196 MeRIP-seq:(Medium) rs751658546 Functional Loss DEL dbSNP153 12..33 33 - - - RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86121 RMVar_ID_86121 Human_SNP_ID_52428011 m1A Human chr1 + 227735196 227735196 227735196 CCCGGCTCCGAGACGAAGGCTACCCGGCCCGGAGCCTGGCCGACGCCGGGGACATCGACCCCCAG CCCGGCTCCGAGACGAAGGCTACCCGGCCCGGTGCCTGGCCGACGCCGGGGACATCGACCCCCAG A T SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227735153..227735228 26863196 MeRIP-seq:(Medium) rs778543835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86122 RMVar_ID_86122 Human_SNP_ID_52428030 m1A Human chr1 - 227735218 227735218 227735218 CGCCGACAGCCACTTCCGAGGCCTGGGGGTCGATGTCCCCGGCGTCGGCCAGGCTCCGGGCCGGG CGCCGACAGCCACTTCCGAGGCCTGGGGGTCGGTGTCCCCGGCGTCGGCCAGGCTCCGGGCCGGG T C JMJD4 Ensembl:ENSG00000081692 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs753572254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223591,Human_RBP_ID_4029552 86123 RMVar_ID_86123 Human_SNP_ID_52428361 m1A Human chr1 + 227735712 227735712 227735712 GGAGTGCGGCGGTGCGGGGGCGCCCAGGGATGATGGGACCCGGAGAGAACGGTGGGACCCAGAGG GGAGTGCGGCGGTGCGGGGGCGCCCAGGGATGCTGGGACCCGGAGAGAACGGTGGGACCCAGAGG A C SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227735667..227736239 26863196 MeRIP-seq:(Medium) rs1052174458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330557,Human_RBP_ID_8167341,Human_RBP_ID_18928955 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86124 RMVar_ID_86124 Human_SNP_ID_52428362 m1A Human chr1 + 227735712 227735712 227735712 GGAGTGCGGCGGTGCGGGGGCGCCCAGGGATGATGGGACCCGGAGAGAACGGTGGGACCCAGAGG GGAGTGCGGCGGTGCGGGGGCGCCCAGGGATGGTGGGACCCGGAGAGAACGGTGGGACCCAGAGG A G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227735667..227736239 26863196 MeRIP-seq:(Medium) rs1052174458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330557,Human_RBP_ID_8167341,Human_RBP_ID_18928955 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86125 RMVar_ID_86125 Human_SNP_ID_52428386 m1A Human chr1 + 227735819 227735819 227735819 GTAGGGTCCTGGAGGAGATGGTGGGGACCTGGAGAGGACGGTGGCACTTGGAGGGGATGGAGACG GTAGGGTCCTGGAGGAGATGGTGGGGACCTGGGGAGGACGGTGGCACTTGGAGGGGATGGAGACG A G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:227735672..227736240 26863196 MeRIP-seq:(Medium) rs1215158327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167342,Human_RBP_ID_9412175 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86126 RMVar_ID_86126 Human_SNP_ID_52429735 m1A Human chr1 + 227740739 227740739 227740739 GAGGGTGGGGACACAGCTGCCAGGACATGCTCATGGCATGTTTCTTGAGGGGGAGGAAGAGAGGA GAGGGTGGGGACACAGCTGCCAGGACATGCTCGTGGCATGTTTCTTGAGGGGGAGGAAGAGAGGA A G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227740728..227741394 26863196 MeRIP-seq:(Medium) rs150157594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804208 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86127 RMVar_ID_86127 Human_SNP_ID_52429736 m1A Human chr1 + 227740739 227740739 227740739 GAGGGTGGGGACACAGCTGCCAGGACATGCTCATGGCATGTTTCTTGAGGGGGAGGAAGAGAGGA GAGGGTGGGGACACAGCTGCCAGGACATGCTCTTGGCATGTTTCTTGAGGGGGAGGAAGAGAGGA A T SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227740728..227741394 26863196 MeRIP-seq:(Medium) rs150157594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804208 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86128 RMVar_ID_86128 Human_SNP_ID_52429991 m1A Human chr1 + 227741636 227741636 227741636 GGTCTGGGGGCTGAGAGAGAGAGGGTGGGATCAGGGCCCCGGGAGGAGGGTCTGGCCTTGGAGGT GGTCTGGGGGCTGAGAGAGAGAGGGTGGGATCGGGGCCCCGGGAGGAGGGTCTGGCCTTGGAGGT A G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227741628..227741732 26863196 MeRIP-seq:(Medium) rs1412744006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328859,Human_RBP_ID_8051905,Human_RBP_ID_8167345 RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 86129 RMVar_ID_86129 Human_SNP_ID_52442000 m1A Human chr1 + 227788582 227788582 227788582 GGGGAGATGCGGGCTCCTCCAGGTAGCGCAGGAGCCCCTCCGGCTGCCGGAGCCCCGCGAGGGCG GGGGAGATGCGGGCTCCTCCAGGTAGCGCAGGTGCCCCTCCGGCTGCCGGAGCCCCGCGAGGGCG A T AL731702.1 Ensembl:ENSG00000286389 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227788410..227788754 26863196 MeRIP-seq:(Medium) rs1362702015 Functional Loss SNV dbSNP153 33..33 33 - - - 86130 RMVar_ID_86130 Human_SNP_ID_52468803 m1A Human chr1 + 227899536 227899536 227899536 CTTGCAAAGTGGCAGGTGCAGGTGCTCACGCCAGGCTCGGCAGCCCCCAGTCTGCTTTGCGGCTC CTTGCAAAGTGGCAGGTGCAGGTGCTCACGCCCGGCTCGGCAGCCCCCAGTCTGCTTTGCGGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227899533..227899786 26863196 MeRIP-seq:(Medium) rs946112338 Functional Loss SNV dbSNP153 33..33 33 - - - 86131 RMVar_ID_86131 Human_SNP_ID_52468843 m1A Human chr1 - 227899634 227899632 227899634 GACAGAGGGGGGAAGCAGAGAGACAGAGACAGAGGGAGACAGAGAGTGGCAGAGAGGTAAGACAG GACAGAGGGGGGAAGCAGAGAGACAGAGACAG__GGAGACAGAGAGTGGCAGAGAGGTAAGACAG CCT C lnc-WNT9A-2,lnc-WNT9A-2:2,lnc-WNT9A-2:3 RNACentral:URS00008BFCB9,RNACentral:URS00008B6A1B,RNACentral:URS0000E91176 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227899532..227899738 26863196 MeRIP-seq:(Medium) rs970487384 Functional Loss DEL dbSNP153 33..34 33 - - - 86132 RMVar_ID_86132 Human_SNP_ID_52474244 m1A Human chr1 - 227918310 227918310 227918310 AGGAGGAGGACCCTGGGGAGGAGGGCCTGGGGAAAGAGGAGGACCTGGGGAGGAGAAGGGCCCTT AGGAGGAGGACCCTGGGGAGGAGGGCCTGGGGGAAGAGGAGGACCTGGGGAGGAGAAGGGCCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227918263..227918356 26863196 MeRIP-seq:(Medium) rs960234210 Functional Loss SNV dbSNP153 33..33 33 - - - 86133 RMVar_ID_86133 Human_SNP_ID_52474735 m1A Human chr1 + 227919854 227919853 227919855 ACACTGACCACGCCAGCACACACACTCTCACAACACACACACACACTACACCCTCAAACCAAGCC ACACTGACCACGCCAGCACACACACTCTCACA__ACACACACACACTACACCCTCAAACCAAGCC AAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227919803..227920070 26863196 MeRIP-seq:(Medium) rs71559823 Functional Loss DEL dbSNP153 33..34 33 - - - 86134 RMVar_ID_86134 Human_SNP_ID_52476126 m1A Human chr1 - 227924227 227924227 227924227 GGGGGGGCTGCGGAGACAACCTTAAGTACAGCAGCAAGTTCGTCAAGGAATTCCTGGGCAGACGG GGGGGGGCTGCGGAGACAACCTTAAGTACAGCCGCAAGTTCGTCAAGGAATTCCTGGGCAGACGG T G WNT9A Ensembl:ENSG00000143816 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227921881..227924267 26863196 MeRIP-seq:(Medium) rs147024660 Functional Loss SNV dbSNP153 33..33 33 - - - 86135 RMVar_ID_86135 Human_SNP_ID_52476545 m1A Human chr1 - 227925427 227925422 227925428 CCAGGCGCACTACAAGGCCTGCGACCGGCTGAAGCTGGAGCGGAAGCAGCGGCGCATGTGCCGCC CCAGGCGCACTACAAGGCCTGCGACCGGCTG______GAGCGGAAGCAGCGGCGCATGTGCCGCC CCAGCTT C WNT9A Ensembl:ENSG00000143816 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227925376..227947898 26863196 MeRIP-seq:(Medium) rs1422770955 Functional Loss DEL dbSNP153 32..37 33 - - - Human_Splice_Rec_194434 86136 RMVar_ID_86136 Human_SNP_ID_52476736 m1A Human chr1 + 227926046 227926046 227926046 TACAGTCCTGTGGCCCCCTGCAGCTTCCCAGCACTCCTGCAGTCTACGCATATGTCCCCAGGTTC TACAGTCCTGTGGCCCCCTGCAGCTTCCCAGCCCTCCTGCAGTCTACGCATATGTCCCCAGGTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227926044..227926546 26863196 MeRIP-seq:(Medium) rs1469706366 Functional Loss SNV dbSNP153 33..33 33 - - - 86137 RMVar_ID_86137 Human_SNP_ID_52483776 m1A Human chr1 + 227953149 227953146 227953149 AAAGATGAAGAGAGAGAATGAGAGGGAGACAAAAGAGACAGATGGAGAGAGATACGAAGACAGAG AAAGATGAAGAGAGAGAATGAGAGGGAGAC___AGAGACAGATGGAGAGAGATACGAAGACAGAG CAAA C LOC107985355-001 RNACentral:URS0000D5D986 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227953073..227953303 26863196 MeRIP-seq:(Medium) rs1043233105 Functional Loss DEL dbSNP153 31..33 33 - - - 86138 RMVar_ID_86138 Human_SNP_ID_52483777 m1A Human chr1 + 227953149 227953146 227953149 AAAGATGAAGAGAGAGAATGAGAGGGAGACAAAAGAGACAGATGGAGAGAGATACGAAGACAGAG AAAGATGAAGAGAGAGAATGAGAGGGAGACA__AGAGACAGATGGAGAGAGATACGAAGACAGAG CAAA CA LOC107985355-001 RNACentral:URS0000D5D986 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227953073..227953303 26863196 MeRIP-seq:(Medium) rs1043233105 Functional Loss DEL dbSNP153 32..33 33 - - - 86139 RMVar_ID_86139 Human_SNP_ID_52488499 m1A Human chr1 + 227971424 227971424 227971424 AATGGTCTCCGGTCGGTGGGCTCCTCCACGCCAAGCTTGGGCCTCCCGGCGACCTCTGCAGACCC AATGGTCTCCGGTCGGTGGGCTCCTCCACGCCCAGCTTGGGCCTCCCGGCGACCTCTGCAGACCC A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200489028 Functional Loss SNV dbSNP153 33..33 33 - - - 86140 RMVar_ID_86140 Human_SNP_ID_52516529 m1A Human chr1 + 228082756 228082756 228082756 GGGAGCAAAACCAACGCCTGGCTCGGAGCAGCAGCCTCTGAGGTGAGGGCGAGGGGCGCGGGCCG GGGAGCAAAACCAACGCCTGGCTCGGAGCAGCGGCCTCTGAGGTGAGGGCGAGGGGCGCGGGCCG A G ARF1 Ensembl:ENSG00000143761 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228082701..228083456 26863196 MeRIP-seq:(Medium) rs1033360171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423023,Human_RBP_ID_4074804,Human_RBP_ID_5312004,Human_RBP_ID_5413624,Human_RBP_ID_5773186,Human_RBP_ID_18187379,Human_RBP_ID_18565327,Human_RBP_ID_19036010,Human_RBP_ID_22430023,Human_RBP_ID_22532182 Human_Splice_Rec_194445,Human_Splice_Rec_194453,Human_Splice_Rec_194461,Human_Splice_Rec_194467,Human_Splice_Rec_194475,Human_Splice_Rec_194483 86141 RMVar_ID_86141 Human_SNP_ID_52516535 m1A Human chr1 - 228082762 228082762 228082762 CCACACCGGCCCGCGCCCCTCGCCCTCACCTCAGAGGCTGCTGCTCCGAGCCAGGCGTTGGTTTT CCACACCGGCCCGCGCCCCTCGCCCTCACCTCGGAGGCTGCTGCTCCGAGCCAGGCGTTGGTTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:228082701..228082954;chr1:228082701..228083482 26863196 MeRIP-seq:(Medium) rs1448707466 Functional Loss SNV dbSNP153 33..33 33 - - - 86142 RMVar_ID_86142 Human_SNP_ID_52516740 m1A Human chr1 - 228083309 228083309 228083309 GGGAGGCGAAGATGCAAGCCCCCACCACCTACATGACCTTGACGGCGTCTCAGGCCGCCCGAGCC GGGAGGCGAAGATGCAAGCCCCCACCACCTACGTGACCTTGACGGCGTCTCAGGCCGCCCGAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228083307..228083426 32194978 MeRIP-seq:(Medium) rs1009101631 Functional Loss SNV dbSNP153 33..33 33 - - - 86143 RMVar_ID_86143 Human_SNP_ID_52520298 m1A Human chr1 - 228097094 228097094 228097094 GATGTTCCCCATGCTTGTGGACAGGTGGAAGGACACTGGCCAGGGACACCTGGAGAGACAAGGTG GATGTTCCCCATGCTTGTGGACAGGTGGAAGGGCACTGGCCAGGGACACCTGGAGAGACAAGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228097076..228097189 26863196 MeRIP-seq:(Medium) rs377716619 Functional Loss SNV dbSNP153 33..33 33 - - - 86144 RMVar_ID_86144 Human_SNP_ID_52520327 m1A Human chr1 + 228097198 228097198 228097198 ATGCGCATCCTCATGGTGGGCCTGGATGCTGCAGGGAAGACCACGATCCTCTACAAGCTTAAGCT ATGCGCATCCTCATGGTGGGCCTGGATGCTGCGGGGAAGACCACGATCCTCTACAAGCTTAAGCT A G ARF1 Ensembl:ENSG00000143761 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:228097099..228097200 32194978 MeRIP-seq:(Medium) rs775417374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344462,Human_RBP_ID_743337,Human_RBP_ID_1423038,Human_RBP_ID_1739239,Human_RBP_ID_3300860,Human_RBP_ID_3937436,Human_RBP_ID_4029742,Human_RBP_ID_5773379,Human_RBP_ID_8301028,Human_RBP_ID_8964368,Human_RBP_ID_17216305,Human_RBP_ID_18187877,Human_RBP_ID_18565361,Human_RBP_ID_22430024,Human_RBP_ID_23370468,Human_RBP_ID_24361109,Human_RBP_ID_26855569 Human_Splice_Rec_194447,Human_Splice_Rec_194455,Human_Splice_Rec_194469,Human_Splice_Rec_194477,Human_Splice_Rec_194487,Human_Splice_Rec_194495,Human_Splice_Rec_194501,Human_Splice_Rec_194509,Human_Splice_Rec_194517,Human_Splice_Rec_194527,Human_Splice_Rec_194535,Human_Splice_Rec_194543 Human_miRNA_ID_1936052,Human_miRNA_ID_1947152 RMVar_hsa_circ_10532,RMVar_hsa_circ_110774,RMVar_hsa_circ_300880,RMVar_hsa_circ_140215,RMVar_hsa_circ_140216 86145 RMVar_ID_86145 Human_SNP_ID_52520558 m1A Human chr1 + 228097887 228097887 228097887 CTCCCCAACGCCATGAATGCGGCCGAGATCACAGACAAGCTGGGGCTGCACTCACTACGCCACAG CTCCCCAACGCCATGAATGCGGCCGAGATCACGGACAAGCTGGGGCTGCACTCACTACGCCACAG A G ARF1 Ensembl:ENSG00000143761 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:228097701..228098075 26863196 MeRIP-seq:(Medium) rs1182740197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344479,Human_RBP_ID_975602,Human_RBP_ID_1423050,Human_RBP_ID_1739247,Human_RBP_ID_4090296,Human_RBP_ID_5155952,Human_RBP_ID_5773397,Human_RBP_ID_8240552,Human_RBP_ID_8301039,Human_RBP_ID_10823248,Human_RBP_ID_17216310,Human_RBP_ID_17333788,Human_RBP_ID_17741628,Human_RBP_ID_18187384,Human_RBP_ID_18565373,Human_RBP_ID_22427850,Human_RBP_ID_22487218,Human_RBP_ID_22782591,Human_RBP_ID_23370476,Human_RBP_ID_26376424,Human_RBP_ID_26855575,Human_RBP_ID_27177125 Human_Splice_Rec_194452,Human_Splice_Rec_194460,Human_Splice_Rec_194466,Human_Splice_Rec_194474,Human_Splice_Rec_194482,Human_Splice_Rec_194492,Human_Splice_Rec_194506,Human_Splice_Rec_194514,Human_Splice_Rec_194522,Human_Splice_Rec_194532,Human_Splice_Rec_194540 Human_miRNA_ID_866440 RMVar_hsa_circ_110774,RMVar_hsa_circ_140216,RMVar_hsa_circ_94497,RMVar_hsa_circ_140217 86146 RMVar_ID_86146 Human_SNP_ID_52520780 m1A Human chr1 - 228098551 228098548 228098551 CAGAATTGATCGCAGTCTGCTGCGCCACCACCACCTCATGTTCCCGAGGGGAACAGCTGGGCTGG CAGAATTGATCGCAGTCTGCTGCGCCACCACC___TCATGTTCCCGAGGGGAACAGCTGGGCTGG AGGT A HSALNG0011193 RNACentral:URS0000EAC7E3 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228098501..228098950 32194978 MeRIP-seq:(Medium) rs1353977584 Functional Loss DEL dbSNP153 33..35 33 - - - 86147 RMVar_ID_86147 Human_SNP_ID_52520897 m1A Human chr1 + 228098839 228098839 228098839 CCCAACACTCGTGCTCGCTCAGACACTTTGGCAGGATGTCTGGGGCCTCACCAGCAGGAGCGCGT CCCAACACTCGTGCTCGCTCAGACACTTTGGCGGGATGTCTGGGGCCTCACCAGCAGGAGCGCGT A G ARF1 Ensembl:ENSG00000143761 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228098790..228098903 26863196 MeRIP-seq:(Medium) rs912353393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344483,Human_RBP_ID_1423077,Human_RBP_ID_1739257,Human_RBP_ID_3300873,Human_RBP_ID_5253329,Human_RBP_ID_5773446,Human_RBP_ID_8301067,Human_RBP_ID_10823305,Human_RBP_ID_17741649,Human_RBP_ID_18225537,Human_RBP_ID_18565391,Human_RBP_ID_22782605,Human_RBP_ID_23122241,Human_RBP_ID_23147382,Human_RBP_ID_26376472,Human_RBP_ID_27177141 RMVar_hsa_circ_110774,RMVar_hsa_circ_140216,RMVar_hsa_circ_94497,RMVar_hsa_circ_140217 86148 RMVar_ID_86148 Human_SNP_ID_52521841 m1A Human chr1 - 228101414 228101414 228101414 GGAGAAGAAGAAAAAGAAAAAGAGGAAACACAAGAAAGAGAAGAAGAAGAAAGACAAAGAGCACA GGAGAAGAAGAAAAAGAAAAAGAGGAAACACAGGAAAGAGAAGAAGAAGAAAGACAAAGAGCACA T C C1orf35 Ensembl:ENSG00000143793 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228101171..228101492 26863196 MeRIP-seq:(Medium) rs767052631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21567,Human_RBP_ID_850924,Human_RBP_ID_4090346,Human_RBP_ID_26312852,Human_RBP_ID_27799338 Human_Splice_Rec_194551,Human_Splice_Rec_194562,Human_Splice_Rec_194563,Human_Splice_Rec_194576,Human_Splice_Rec_194577,Human_Splice_Rec_194592,Human_Splice_Rec_194593,Human_Splice_Rec_194602 RMVar_hsa_circ_91663,RMVar_hsa_circ_140218 86149 RMVar_ID_86149 Human_SNP_ID_52522659 m1A Human chr1 - 228103178 228103178 228103178 TGGAGGCGTGCGCGGCGGGCAGGACCAGTTCAACTGGGAGGACGTGAAGACTGACAAGCAGCGGG TGGAGGCGTGCGCGGCGGGCAGGACCAGTTCAGCTGGGAGGACGTGAAGACTGACAAGCAGCGGG T C C1orf35 Ensembl:ENSG00000143793 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:228103126..228103308 26863196 MeRIP-seq:(Medium) rs1238161895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423106,Human_RBP_ID_1739270,Human_RBP_ID_4074807,Human_RBP_ID_5458566,Human_RBP_ID_5773488,Human_RBP_ID_10823384,Human_RBP_ID_18410008,Human_RBP_ID_18415723,Human_RBP_ID_18565423,Human_RBP_ID_22025667,Human_RBP_ID_23122244,Human_RBP_ID_23370522,Human_RBP_ID_26315531 Human_Splice_Rec_194545,Human_Splice_Rec_194553,Human_Splice_Rec_194565,Human_Splice_Rec_194579,Human_Splice_Rec_194613 86150 RMVar_ID_86150 Human_SNP_ID_52523700 m1A Human chr1 + 228106752 228106752 228106752 CTCCCATCTTAGCAATGTCCCGGGGTGGCTGGAGCCACGGTCACTTCTTGGTCCTGGTCCAGAAC CTCCCATCTTAGCAATGTCCCGGGGTGGCTGGGGCCACGGTCACTTCTTGGTCCTGGTCCAGAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:228106701..228106775 32194978 MeRIP-seq:(Medium) rs772608069 Functional Loss SNV dbSNP153 33..33 33 - - - 86151 RMVar_ID_86151 Human_SNP_ID_52523738 m1A Human chr1 - 228106840 228106840 228106840 GGCTGCGGAAGCGTGAGGCTCAGCTCCAGTCGAGGAAGGAGTACGAGCAGGAGCTCAGTGATGAC GGCTGCGGAAGCGTGAGGCTCAGCTCCAGTCGGGGAAGGAGTACGAGCAGGAGCTCAGTGATGAC T C MRPL55 Ensembl:ENSG00000162910 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228106728..228106900 32194978 MeRIP-seq:(Medium) rs976779603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344554,Human_RBP_ID_22782643,Human_RBP_ID_22871896 Human_Splice_Rec_194618,Human_Splice_Rec_194624,Human_Splice_Rec_194628,Human_Splice_Rec_194634,Human_Splice_Rec_194640,Human_Splice_Rec_194644,Human_Splice_Rec_194652,Human_Splice_Rec_194660,Human_Splice_Rec_194666,Human_Splice_Rec_194674,Human_Splice_Rec_194682,Human_Splice_Rec_194688,Human_Splice_Rec_194696,Human_Splice_Rec_194702,Human_Splice_Rec_194710,Human_Splice_Rec_194716,Human_Splice_Rec_194726,Human_Splice_Rec_194734,Human_Splice_Rec_194742,Human_Splice_Rec_194752,Human_Splice_Rec_194760,Human_Splice_Rec_194770 86152 RMVar_ID_86152 Human_SNP_ID_52524231 m1A Human chr1 - 228108286 228108286 228108286 GTTGCACGCCAGGGCCTGTACTGACCACCTCCACGTGCCACTGGGGCTGTAAGGAGGAATGGCGG GTTGCACGCCAGGGCCTGTACTGACCACCTCCTCGTGCCACTGGGGCTGTAAGGAGGAATGGCGG T A MRPL55 Ensembl:ENSG00000162910 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:228108220..228108320 32194978 MeRIP-seq:(Medium) rs1383927242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344558,Human_RBP_ID_850934,Human_RBP_ID_1347076,Human_RBP_ID_1423128,Human_RBP_ID_4074811,Human_RBP_ID_5338967,Human_RBP_ID_5458644,Human_RBP_ID_5485598,Human_RBP_ID_8301104,Human_RBP_ID_10823534,Human_RBP_ID_18565439,Human_RBP_ID_18966481,Human_RBP_ID_22782647,Human_RBP_ID_24749054 Human_Splice_Rec_194619,Human_Splice_Rec_194626,Human_Splice_Rec_194630,Human_Splice_Rec_194631,Human_Splice_Rec_194636,Human_Splice_Rec_194637,Human_Splice_Rec_194641,Human_Splice_Rec_194648,Human_Splice_Rec_194649,Human_Splice_Rec_194654,Human_Splice_Rec_194655,Human_Splice_Rec_194662,Human_Splice_Rec_194663,Human_Splice_Rec_194670,Human_Splice_Rec_194671,Human_Splice_Rec_194678,Human_Splice_Rec_194679,Human_Splice_Rec_194684,Human_Splice_Rec_194685,Human_Splice_Rec_194692,Human_Splice_Rec_194693,Human_Splice_Rec_194698,Human_Splice_Rec_194699,Human_Splice_Rec_194706,Human_Splice_Rec_194707,Human_Splice_Rec_194712,Human_Splice_Rec_194713,Human_Splice_Rec_194720,Human_Splice_Rec_194721,Human_Splice_Rec_194730,Human_Splice_Rec_194731,Human_Splice_Rec_194738,Human_Splice_Rec_194739,Human_Splice_Rec_194746,Human_Splice_Rec_194747,Human_Splice_Rec_194756,Human_Splice_Rec_194757,Human_Splice_Rec_194766,Human_Splice_Rec_194767,Human_Splice_Rec_194776,Human_Splice_Rec_194777,Human_Splice_Rec_194780,Human_Splice_Rec_194781,Human_Splice_Rec_194784,Human_Splice_Rec_194785,Human_Splice_Rec_194792,Human_Splice_Rec_194793,Human_Splice_Rec_194796,Human_Splice_Rec_194800,Human_Splice_Rec_194802,Human_Splice_Rec_194804,Human_Splice_Rec_194810,Human_Splice_Rec_194814,Human_Splice_Rec_194818 RMVar_hsa_circ_345814 86153 RMVar_ID_86153 Human_SNP_ID_52531613 m1A Human chr1 - 228140332 228140320 228140332 CCGTCCGGTGGGGCCCGGCCCAGGGCGGCCGCAGCCAGCCCGGCCAGCGGGCGCCGCAGCATCCG CCGTCCGGTGGGGCCCGGCCCAGGGCGGCCGC____________CAGCGGGCGCCGCAGCATCCG GGCCGGGCTGGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:228140251..228140468;chr1:228140226..228141240;chr1:228140022..228140470;chr1:228140251..228140498 26863196 MeRIP-seq:(Medium) rs1316312896 Functional Loss DEL dbSNP153 33..44 33 - - - 86154 RMVar_ID_86154 Human_SNP_ID_52531638 m1A Human chr1 + 228140356 228140356 228140356 GGGCTGGCTGCGGCCGCCCTGGGCCGGGCCCCACCGGACGGTGAGTACGACAAGCGCGATCGCGA GGGCTGGCTGCGGCCGCCCTGGGCCGGGCCCCCCCGGACGGTGAGTACGACAAGCGCGATCGCGA A C GUK1 Ensembl:ENSG00000143774 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:228140251..228141187 26863410 MeRIP-seq:(Medium) rs1218082931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073308,Human_RBP_ID_5109818,Human_RBP_ID_5136505,Human_RBP_ID_18415724,Human_RBP_ID_19040362,Human_RBP_ID_22024321,Human_RBP_ID_22871070 Human_Splice_Rec_194835,Human_Splice_Rec_194845,Human_Splice_Rec_194859,Human_Splice_Rec_194869,Human_Splice_Rec_194881,Human_Splice_Rec_194883,Human_Splice_Rec_194889,Human_Splice_Rec_194903,Human_Splice_Rec_194919,Human_Splice_Rec_194935,Human_Splice_Rec_194947,Human_Splice_Rec_194961,Human_Splice_Rec_194975,Human_Splice_Rec_194987,Human_Splice_Rec_195001,Human_Splice_Rec_195013,Human_Splice_Rec_195027 86155 RMVar_ID_86155 Human_SNP_ID_52532553 m1A Human chr1 + 228143673 228143673 228143673 GGCTCGCTGGCTGGGAGAAGCTGAATGGATAAAGAACCCTGGCCACTGCAGTGCGTGCTGATGGT GGCTCGCTGGCTGGGAGAAGCTGAATGGATAATGAACCCTGGCCACTGCAGTGCGTGCTGATGGT A T GUK1 Ensembl:ENSG00000143774 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228143670..228143766 26863196 MeRIP-seq:(Medium) rs1246058795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328891,Human_RBP_ID_5234418,Human_RBP_ID_5641917,Human_RBP_ID_8051949,Human_RBP_ID_8301122,Human_RBP_ID_10823661,Human_RBP_ID_18455251,Human_RBP_ID_18565450,Human_RBP_ID_21963360,Human_RBP_ID_23263322 RMVar_hsa_circ_128014,RMVar_hsa_circ_140219 86156 RMVar_ID_86156 Human_SNP_ID_52533596 m1A Human chr1 + 228147468 228147468 228147468 GAACCGCATCTGTGTGCTGGACGTGGACCTGCAGGGTGTGCGGAACATCAAGGCCACCGATCTGC GAACCGCATCTGTGTGCTGGACGTGGACCTGCTGGGTGTGCGGAACATCAAGGCCACCGATCTGC A T GUK1 Ensembl:ENSG00000143774 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1369476188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344599,Human_RBP_ID_1739287,Human_RBP_ID_3934619,Human_RBP_ID_5773555,Human_RBP_ID_8301133,Human_RBP_ID_9357645,Human_RBP_ID_18187882,Human_RBP_ID_22024323,Human_RBP_ID_23122249,Human_RBP_ID_26799540 Human_Splice_Rec_194828,Human_Splice_Rec_194829,Human_Splice_Rec_194842,Human_Splice_Rec_194843,Human_Splice_Rec_194852,Human_Splice_Rec_194853,Human_Splice_Rec_194876,Human_Splice_Rec_194877,Human_Splice_Rec_194896,Human_Splice_Rec_194897,Human_Splice_Rec_194912,Human_Splice_Rec_194913,Human_Splice_Rec_194928,Human_Splice_Rec_194929,Human_Splice_Rec_194942,Human_Splice_Rec_194943,Human_Splice_Rec_194954,Human_Splice_Rec_194955,Human_Splice_Rec_194968,Human_Splice_Rec_194969,Human_Splice_Rec_194994,Human_Splice_Rec_194995,Human_Splice_Rec_195010,Human_Splice_Rec_195011,Human_Splice_Rec_195022,Human_Splice_Rec_195023,Human_Splice_Rec_195034,Human_Splice_Rec_195035,Human_Splice_Rec_195056,Human_Splice_Rec_195057,Human_Splice_Rec_195070,Human_Splice_Rec_195078,Human_Splice_Rec_195079,Human_Splice_Rec_195090,Human_Splice_Rec_195091,Human_Splice_Rec_195098,Human_Splice_Rec_195099,Human_Splice_Rec_195108,Human_Splice_Rec_195109,Human_Splice_Rec_195120,Human_Splice_Rec_195126,Human_Splice_Rec_195132,Human_Splice_Rec_195133,Human_Splice_Rec_195142,Human_Splice_Rec_195143,Human_Splice_Rec_195150,Human_Splice_Rec_195151,Human_Splice_Rec_195158,Human_Splice_Rec_195159,Human_Splice_Rec_195162,Human_Splice_Rec_195165 RMVar_hsa_circ_3447,RMVar_hsa_circ_84116,RMVar_hsa_circ_140220,RMVar_hsa_circ_17856,RMVar_hsa_circ_140221 86157 RMVar_ID_86157 Human_SNP_ID_52533720 m1A Human chr1 - 228147712 228147712 228147712 TGACTCCCCTCCTGGCATTCCCTGGTGATCCCACGGCACACTCACTGCTCTCCATGTCGGCCTGG TGACTCCCCTCCTGGCATTCCCTGGTGATCCCTCGGCACACTCACTGCTCTCCATGTCGGCCTGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228147708..228148188 32194978 MeRIP-seq:(Medium) rs772063694 Functional Loss SNV dbSNP153 33..33 33 - - - 86158 RMVar_ID_86158 Human_SNP_ID_52533931 m1A Human chr1 - 228148338 228148338 228148338 CTGTGGGTGGGGCCTGGGGTCAGGGCACAGTGAGCCCATGCAGCCCCACCCCAGGTCCCACACGA CTGTGGGTGGGGCCTGGGGTCAGGGCACAGTGGGCCCATGCAGCCCCACCCCAGGTCCCACACGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228148336..228148483 26863196 MeRIP-seq:(Medium) rs1248087231 Functional Loss SNV dbSNP153 33..33 33 - - - 86159 RMVar_ID_86159 Human_SNP_ID_52534130 m1A Human chr1 + 228148863 228148863 228148863 TGGTTGGAACATCCTGGGGTGACCCCCGACCCAGCCTCGCTGGGCTGTCCCCTGTCCCTATCTCT TGGTTGGAACATCCTGGGGTGACCCCCGACCCGGCCTCGCTGGGCTGTCCCCTGTCCCTATCTCT A G GUK1 Ensembl:ENSG00000143774 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228148812..228148896 26863196 MeRIP-seq:(Medium) rs964424215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224188,Human_RBP_ID_258583,Human_RBP_ID_344617,Human_RBP_ID_745119,Human_RBP_ID_8240554,Human_RBP_ID_17647875,Human_RBP_ID_17741697,Human_RBP_ID_18565468,Human_RBP_ID_26312862,Human_RBP_ID_27177224 Human_miRNA_ID_1393862 86160 RMVar_ID_86160 Human_SNP_ID_52536376 m1A Human chr1 - 228157312 228157312 228157312 CCCCTCCAGCTCCCTAGCCCCCAAGCCCCTGCAGCCCCATCAGCCCTCAGTCCTTCACAGCCCCC CCCCTCCAGCTCCCTAGCCCCCAAGCCCCTGCTGCCCCATCAGCCCTCAGTCCTTCACAGCCCCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228157136..228157378 26863196 MeRIP-seq:(Medium) rs141093786 Functional Loss SNV dbSNP153 33..33 33 - - - 86161 RMVar_ID_86161 Human_SNP_ID_52536742 m1A Human chr1 - 228158198 228158198 228158198 CCTCCTCCTCCTCCTCCTCGCCCAGGCCCAGCATGGGCTCCTCCTCGCCCAGGTCGGCGGGCTCA CCTCCTCCTCCTCCTCCTCGCCCAGGCCCAGCGTGGGCTCCTCCTCGCCCAGGTCGGCGGGCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228158162..228158384 26863196 MeRIP-seq:(Medium) rs908269724 Functional Loss SNV dbSNP153 33..33 33 - - - 86162 RMVar_ID_86162 Human_SNP_ID_52537264 m1A Human chr1 - 228159191 228159191 228159191 CTTCCCTGAGCAGCCTGGCTGCCCCTCTGGGCAGAGTCTGCCTGAGGCCACCGGCTAAGGAGAAG CTTCCCTGAGCAGCCTGGCTGCCCCTCTGGGCGGAGTCTGCCTGAGGCCACCGGCTAAGGAGAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228159155..228159301 26863196 MeRIP-seq:(Medium) rs927432598 Functional Loss SNV dbSNP153 33..33 33 - - - 86163 RMVar_ID_86163 Human_SNP_ID_52542647 m1A Human chr1 + 228176802 228176802 228176802 AAAGGCAGCTCTGAGCTGCAGTGTAGTTTGTGATCACCCAGGAGGAGGGTGTAGAGCGGATGGAC AAAGGCAGCTCTGAGCTGCAGTGTAGTTTGTGGTCACCCAGGAGGAGGGTGTAGAGCGGATGGAC A G IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228176772..228176886 26863196 MeRIP-seq:(Medium) rs1432881114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_975646,Human_RBP_ID_5773621,Human_RBP_ID_10823921,Human_RBP_ID_26386992 86164 RMVar_ID_86164 Human_SNP_ID_52544324 m1A Human chr1 - 228182841 228182841 228182841 ACATCTGAGCTCCCAAATTCAGGACCCTCCAGACTGCCTACCCCCAGCTGGGCATCCAACTGCTA ACATCTGAGCTCCCAAATTCAGGACCCTCCAGGCTGCCTACCCCCAGCTGGGCATCCAACTGCTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228182790..228183009 26863196 MeRIP-seq:(Medium) rs970043676 Functional Loss SNV dbSNP153 33..33 33 - - - 86165 RMVar_ID_86165 Human_SNP_ID_52544660 m1A Human chr1 - 228184189 228184188 228184189 CTCACTTGGCCTTTACTCCCTGTGTGCACCCCAGGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT CTCACTTGGCCTTTACTCCCTGTGTGCACCCC_GGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228184151..228184302 32194978 MeRIP-seq:(Medium) rs67091456 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_10290,GWAS_ID_10291,GWAS_ID_10292,GWAS_ID_10293,GWAS_ID_10294,GWAS_ID_10295,GWAS_ID_10296,GWAS_ID_10297,GWAS_ID_10298,GWAS_ID_10299,GWAS_ID_10300,GWAS_ID_10301,GWAS_ID_10302,GWAS_ID_10303,GWAS_ID_10304,GWAS_ID_10305,GWAS_ID_10306,GWAS_ID_10307,GWAS_ID_10308 86166 RMVar_ID_86166 Human_SNP_ID_52544664 m1A Human chr1 - 228184189 228184189 228184189 CTCACTTGGCCTTTACTCCCTGTGTGCACCCCAGGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT CTCACTTGGCCTTTACTCCCTGTGTGCACCCCTGGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228184151..228184302 32194978 MeRIP-seq:(Medium) rs1059777 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10309,GWAS_ID_10310,GWAS_ID_10311,GWAS_ID_10312,GWAS_ID_10313,GWAS_ID_10314,GWAS_ID_10315,GWAS_ID_10316,GWAS_ID_10317,GWAS_ID_10318,GWAS_ID_10319,GWAS_ID_10320,GWAS_ID_10321,GWAS_ID_10322,GWAS_ID_10323 86167 RMVar_ID_86167 Human_SNP_ID_52544665 m1A Human chr1 - 228184189 228184189 228184189 CTCACTTGGCCTTTACTCCCTGTGTGCACCCCAGGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT CTCACTTGGCCTTTACTCCCTGTGTGCACCCCGGGGGGTCTTTTTGTGTGTCCAGATTTCTTCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228184151..228184302 32194978 MeRIP-seq:(Medium) rs1059777 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10309,GWAS_ID_10310,GWAS_ID_10311,GWAS_ID_10312,GWAS_ID_10313,GWAS_ID_10314,GWAS_ID_10315,GWAS_ID_10316,GWAS_ID_10317,GWAS_ID_10318,GWAS_ID_10319,GWAS_ID_10320,GWAS_ID_10321,GWAS_ID_10322,GWAS_ID_10323 86168 RMVar_ID_86168 Human_SNP_ID_52551544 m1A Human chr1 + 228212658 228212658 228212658 CCGGCGCCACGTGGTGTACGAGGACGCGCAGGAGAACTTCGTGCTCAAGATCCTCTTCTGCAAGC CCGGCGCCACGTGGTGTACGAGGACGCGCAGGGGAACTTCGTGCTCAAGATCCTCTTCTGCAAGC A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228212607..228212705 26863196 MeRIP-seq:(Medium) rs772783924 Functional Loss SNV dbSNP153 33..33 33 - - - 86169 RMVar_ID_86169 Human_SNP_ID_52551912 m1A Human chr1 - 228213507 228213507 228213507 CCTCAGTGGACGGCTGGGGCACCTCACATAGGAACGTGGCCGACTCCTTCTCCCGCACCTCCAGA CCTCAGTGGACGGCTGGGGCACCTCACATAGGCACGTGGCCGACTCCTTCTCCCGCACCTCCAGA T G OBSCN-AS1 Ensembl:ENSG00000162913 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228213456..228214292 32194978 MeRIP-seq:(Medium) rs1222675311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_195195,Human_Splice_Rec_195199,Human_Splice_Rec_195211,Human_Splice_Rec_195217,Human_Splice_Rec_195223 86170 RMVar_ID_86170 Human_SNP_ID_52553085 m1A Human chr1 - 228216433 228216433 228216433 GGGCAGCTGCGGCTGGCGGCTTGTTGGCAGTCAGCCCTGGGGCCGCTGGGGGCCAGGTATGCGTG GGGCAGCTGCGGCTGGCGGCTTGTTGGCAGTCGGCCCTGGGGCCGCTGGGGGCCAGGTATGCGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228216383..228216546 26863196 MeRIP-seq:(Medium) rs1212582692 Functional Loss SNV dbSNP153 33..33 33 - - - 86171 RMVar_ID_86171 Human_SNP_ID_52553363 m1A Human chr1 + 228217103 228217103 228217103 GGGCCCGGCGCAGTTTGAGTGTGAGACCTCCGAAGCCCACGTCCACGTGCACTGGTACAAGGATG GGGCCCGGCGCAGTTTGAGTGTGAGACCTCCGCAGCCCACGTCCACGTGCACTGGTACAAGGATG A C OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228217006..228217224 26863196 MeRIP-seq:(Medium) rs567470852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934625,Human_RBP_ID_18565513 Human_Splice_Rec_195236,Human_Splice_Rec_195394,Human_Splice_Rec_195600,Human_Splice_Rec_195826,Human_Splice_Rec_195886,Human_Splice_Rec_196102,Human_Splice_Rec_196328,Human_Splice_Rec_196532,Human_Splice_Rec_196732,Human_Splice_Rec_196744 RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_57992,RMVar_hsa_circ_34239 86172 RMVar_ID_86172 Human_SNP_ID_52559137 m1A Human chr1 + 228240332 228240332 228240332 AAAAAAAAGAAAAAAAAAACCAGAGGTGGAGCACAACAGAGTGGTGGCCAGGTGGGTTCAGGGTT AAAAAAAAGAAAAAAAAAACCAGAGGTGGAGCGCAACAGAGTGGTGGCCAGGTGGGTTCAGGGTT A G OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228240329..228240511 26863196 MeRIP-seq:(Medium) rs1420129870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_57992,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_67545 86173 RMVar_ID_86173 Human_SNP_ID_52560522 m1A Human chr1 + 228245542 228245542 228245542 CCAGACAGAGGTGACGTGGTACAAGGACGGGAAGAAGCTGAGCTCCAGCTCAAAAGTACGCATGG CCAGACAGAGGTGACGTGGTACAAGGACGGGAGGAAGCTGAGCTCCAGCTCAAAAGTACGCATGG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228245374..228245650 26863196 MeRIP-seq:(Medium) rs1200440854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_57992,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_67545,RMVar_hsa_circ_125472,RMVar_hsa_circ_43985,RMVar_hsa_circ_69478,RMVar_hsa_circ_140223 86174 RMVar_ID_86174 Human_SNP_ID_52560818 m1A Human chr1 + 228246548 228246548 228246548 GTCCACCCTCAGAGCCCAAGGCAGTGTTTGCCAAGGAGCAGTTGGTGCATAATGAGGTGCGGACT GTCCACCCTCAGAGCCCAAGGCAGTGTTTGCCGAGGAGCAGTTGGTGCATAATGAGGTGCGGACT A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228246536..228256807 32194978 MeRIP-seq:(Medium) rs373610594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22635112 Human_Splice_Rec_195246,Human_Splice_Rec_195404,Human_Splice_Rec_195612,Human_Splice_Rec_195836,Human_Splice_Rec_195896,Human_Splice_Rec_196114,Human_Splice_Rec_196338,Human_Splice_Rec_196542,Human_Splice_Rec_196740 RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_57992,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_67545,RMVar_hsa_circ_125472,RMVar_hsa_circ_69478,RMVar_hsa_circ_140224,RMVar_hsa_circ_140223 86175 RMVar_ID_86175 Human_SNP_ID_52563314 m1A Human chr1 + 228256752 228256752 228256752 CCACACTCAGCTGCGAGGTGGCTCAGGCCCAGACGGAGGTGATGTGGTACAAGGACGGGAAGAAG CCACACTCAGCTGCGAGGTGGCTCAGGCCCAGCCGGAGGTGATGTGGTACAAGGACGGGAAGAAG A C OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228256701..228256900 26863196 MeRIP-seq:(Medium) rs747985826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32576,RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_64814,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225 86176 RMVar_ID_86176 Human_SNP_ID_52563315 m1A Human chr1 + 228256752 228256752 228256752 CCACACTCAGCTGCGAGGTGGCTCAGGCCCAGACGGAGGTGATGTGGTACAAGGACGGGAAGAAG CCACACTCAGCTGCGAGGTGGCTCAGGCCCAGGCGGAGGTGATGTGGTACAAGGACGGGAAGAAG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228256701..228256900 26863196 MeRIP-seq:(Medium) rs747985826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32576,RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_64814,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225 86177 RMVar_ID_86177 Human_SNP_ID_52563349 m1A Human chr1 + 228256809 228256809 228256809 GGAAGAAGCTGAGCTTCAGCTCGAAAGTGCGCATGGAGGCTGTGGGCTGCACACGGAGGCTGGTG GGAAGAAGCTGAGCTTCAGCTCGAAAGTGCGCGTGGAGGCTGTGGGCTGCACACGGAGGCTGGTG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228256761..228256928 26863196 MeRIP-seq:(Medium) rs200775061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32576,RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_64814,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225 86178 RMVar_ID_86178 Human_SNP_ID_52563350 m1A Human chr1 + 228256809 228256809 228256809 GGAAGAAGCTGAGCTTCAGCTCGAAAGTGCGCATGGAGGCTGTGGGCTGCACACGGAGGCTGGTG GGAAGAAGCTGAGCTTCAGCTCGAAAGTGCGCTTGGAGGCTGTGGGCTGCACACGGAGGCTGGTG A T OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228256761..228256928 26863196 MeRIP-seq:(Medium) rs200775061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32576,RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_64814,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225 86179 RMVar_ID_86179 Human_SNP_ID_52565144 m1A Human chr1 - 228264256 228264256 228264256 GCCCACGGCCTCCATTCGCACTTTCGAGCTGGAGCTCAGTTTCTTCCCGTCCTTGTACCACGTCA GCCCACGGCCTCCATTCGCACTTTCGAGCTGGCGCTCAGTTTCTTCCCGTCCTTGTACCACGTCA T G AL353593.1 Ensembl:ENSG00000269934 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228264129..228264427 26863196 MeRIP-seq:(Medium) rs1012060930 Functional Loss SNV dbSNP153 33..33 33 - - - 86180 RMVar_ID_86180 Human_SNP_ID_52567128 m1A Human chr1 - 228272026 228272026 228272026 CATAACCTCCGTCTGGGCTTGGGCCACCTCGCAGCTCAGCATGGTGCTGGTCCCTGCCTCAGCCT CATAACCTCCGTCTGGGCTTGGGCCACCTCGCGGCTCAGCATGGTGCTGGTCCCTGCCTCAGCCT T C AL353593.1 Ensembl:ENSG00000269934 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228268757..228272127 32194978 MeRIP-seq:(Medium) rs764247208 Functional Loss SNV dbSNP153 33..33 33 - - - 86181 RMVar_ID_86181 Human_SNP_ID_52568062 m1A Human chr1 - 228274591 228274591 228274591 TCCTCTGCGACCACGGTGCTCAGCCCAGACATAAACTTCACCACTCGGGGCACTGCAGACAGGAG TCCTCTGCGACCACGGTGCTCAGCCCAGACATTAACTTCACCACTCGGGGCACTGCAGACAGGAG T A AL353593.1 Ensembl:ENSG00000269934 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228274554..228274653 26863196 MeRIP-seq:(Medium) rs989779395 Functional Loss SNV dbSNP153 33..33 33 - - - 86182 RMVar_ID_86182 Human_SNP_ID_52568170 m1A Human chr1 + 228274832 228274832 228274832 AGGCTGAGGGCGCCTCATCCTCTGCTGCCCTGAGGGTCCGAGGTGAGTGTGGGGGGCAGCAGGAT AGGCTGAGGGCGCCTCATCCTCTGCTGCCCTGTGGGTCCGAGGTGAGTGTGGGGGGCAGCAGGAT A T OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228274781..228274880 26863196 MeRIP-seq:(Medium) rs1395846035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_195261,Human_Splice_Rec_195419,Human_Splice_Rec_195633,Human_Splice_Rec_195851,Human_Splice_Rec_195911,Human_Splice_Rec_196135,Human_Splice_Rec_196353,Human_Splice_Rec_196557 RMVar_hsa_circ_363380,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_93687,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140226,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228 86183 RMVar_ID_86183 Human_SNP_ID_52568689 m1A Human chr1 - 228276256 228276256 228276256 CCCAACCCTACGGCCCTTCCAGAGGGCCCGCCACTCCCCTCAGTGTCCCACCTCGCTCCTCCCTC CCCAACCCTACGGCCCTTCCAGAGGGCCCGCCGCTCCCCTCAGTGTCCCACCTCGCTCCTCCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228276249..228276321 26863196 MeRIP-seq:(Medium) rs993744586 Functional Loss SNV dbSNP153 33..33 33 - - - 86184 RMVar_ID_86184 Human_SNP_ID_52568690 m1A Human chr1 - 228276256 228276256 228276256 CCCAACCCTACGGCCCTTCCAGAGGGCCCGCCACTCCCCTCAGTGTCCCACCTCGCTCCTCCCTC CCCAACCCTACGGCCCTTCCAGAGGGCCCGCCCCTCCCCTCAGTGTCCCACCTCGCTCCTCCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228276249..228276321 26863196 MeRIP-seq:(Medium) rs993744586 Functional Loss SNV dbSNP153 33..33 33 - - - 86185 RMVar_ID_86185 Human_SNP_ID_52568844 m1A Human chr1 + 228276534 228276534 228276534 GGGCACGGCTACCATGGAGGTGCAGCTGTCGCATGCGGACGTGGATGGCAGCTGGACTCGTGACG GGGCACGGCTACCATGGAGGTGCAGCTGTCGCCTGCGGACGTGGATGGCAGCTGGACTCGTGACG A C OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228276483..228276575 26863196 MeRIP-seq:(Medium) rs768308597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_195264,Human_Splice_Rec_195422,Human_Splice_Rec_195636,Human_Splice_Rec_195854,Human_Splice_Rec_195914,Human_Splice_Rec_196138,Human_Splice_Rec_196356,Human_Splice_Rec_196560,Human_Splice_Rec_196748 RMVar_hsa_circ_363380,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_93687,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140226,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228 86186 RMVar_ID_86186 Human_SNP_ID_52569437 m1A Human chr1 - 228277649 228277649 228277649 CGCCTGTCCTCGAACCTTCCTGGCGGATGCGCACGTTGTCAGTGGGCCGCAGTTTACTGCCCTCC CGCCTGTCCTCGAACCTTCCTGGCGGATGCGCGCGTTGTCAGTGGGCCGCAGTTTACTGCCCTCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:228277601..228277759 26863196 MeRIP-seq:(Medium) rs1439542586 Functional Loss SNV dbSNP153 33..33 33 - - - 86187 RMVar_ID_86187 Human_SNP_ID_52570551 m1A Human chr1 + 228280293 228280293 228280293 CCACGAGGATGAGGAGGTCGAGTGGTCGCTCAACGGGATGCCCCTGTACAACGACAGCTTCCATG CCACGAGGATGAGGAGGTCGAGTGGTCGCTCAGCGGGATGCCCCTGTACAACGACAGCTTCCATG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228280159..228280294 26863196 MeRIP-seq:(Medium) rs113202278 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_363380,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_93687,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140226,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228,RMVar_hsa_circ_102932,RMVar_hsa_circ_269226,RMVar_hsa_circ_268044,RMVar_hsa_circ_140229 86188 RMVar_ID_86188 Human_SNP_ID_52573634 m1A Human chr1 + 228288804 228288804 228288804 TGAGGCAGGACGGGGCTGTGTGCGAGCTGCAGATCTGTGGCCTGGCTGTGGCAGATGCTGGGGAG TGAGGCAGGACGGGGCTGTGTGCGAGCTGCAGGTCTGTGGCCTGGCTGTGGCAGATGCTGGGGAG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228288684..228292599 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5537461 Human_Splice_Rec_195297,Human_Splice_Rec_195455,Human_Splice_Rec_195671,Human_Splice_Rec_195947,Human_Splice_Rec_196173,Human_Splice_Rec_196389,Human_Splice_Rec_196593,Human_Splice_Rec_196783 RMVar_hsa_circ_363380,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_114219,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228,RMVar_hsa_circ_102932,RMVar_hsa_circ_269226,RMVar_hsa_circ_268044,RMVar_hsa_circ_269610,RMVar_hsa_circ_140229,RMVar_hsa_circ_267468,RMVar_hsa_circ_11932,RMVar_hsa_circ_47431,RMVar_hsa_circ_140230,RMVar_hsa_circ_140231,RMVar_hsa_circ_123534 86189 RMVar_ID_86189 Human_SNP_ID_52573809 m1A Human chr1 - 228289343 228289343 228289343 CTCCCCACAGTCACCCCCATCACCTCCTCTCCACAGTCACCCCCATCACCTCCTCCCCACAGTCA CTCCCCACAGTCACCCCCATCACCTCCTCTCCCCAGTCACCCCCATCACCTCCTCCCCACAGTCA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:228289308..228289437 26863196 MeRIP-seq:(Medium) rs1246804066 Functional Loss SNV dbSNP153 33..33 33 - - - 86190 RMVar_ID_86190 Human_SNP_ID_52576502 m1A Human chr1 + 228298591 228298591 228298591 AGAAGGGTCCTGAGACCCTCAGAGATGGGGGCAGATACAGCCTGAAGCAGGATGGGACGAGGTGT AGAAGGGTCCTGAGACCCTCAGAGATGGGGGCCGATACAGCCTGAAGCAGGATGGGACGAGGTGT A C OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228298553..228298652 26863196 MeRIP-seq:(Medium) rs1288553160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_114219,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228,RMVar_hsa_circ_102932,RMVar_hsa_circ_269226,RMVar_hsa_circ_268044,RMVar_hsa_circ_269610,RMVar_hsa_circ_140229,RMVar_hsa_circ_267468,RMVar_hsa_circ_10026,RMVar_hsa_circ_11932,RMVar_hsa_circ_140230,RMVar_hsa_circ_140231,RMVar_hsa_circ_123534,RMVar_hsa_circ_140232,RMVar_hsa_circ_115041,RMVar_hsa_circ_268744,RMVar_hsa_circ_26719,RMVar_hsa_circ_140233,RMVar_hsa_circ_26892,RMVar_hsa_circ_16610,RMVar_hsa_circ_35564,RMVar_hsa_circ_15849,RMVar_hsa_circ_61789,RMVar_hsa_circ_140234,RMVar_hsa_circ_35734 86191 RMVar_ID_86191 Human_SNP_ID_52582818 m1A Human chr1 - 228318929 228318929 228318929 GCAGGTCACCCTCCTGGGCTGCCTCGGGGGGCAAGCTGGGCTGAGGGGCCTCATCCACAGAGGCT GCAGGTCACCCTCCTGGGCTGCCTCGGGGGGCGAGCTGGGCTGAGGGGCCTCATCCACAGAGGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228318168..228319029 32194978 MeRIP-seq:(Medium) rs1382953259 Functional Loss SNV dbSNP153 33..33 33 - - - 86192 RMVar_ID_86192 Human_SNP_ID_52592872 m1A Human chr1 + 228353303 228353303 228353303 CCAGGCACAGGTCCCAGCCCCCTGCTGGAGGCAGCACCTGTGTGGGCTGGTGGAGGGTAGCCCCT CCAGGCACAGGTCCCAGCCCCCTGCTGGAGGCCGCACCTGTGTGGGCTGGTGGAGGGTAGCCCCT A C OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228353299..228353509 26863196 MeRIP-seq:(Medium) rs538850421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267772,RMVar_hsa_circ_324283 86193 RMVar_ID_86193 Human_SNP_ID_52594778 m1A Human chr1 + 228360184 228360183 228360184 GGAGGGCACCATGGAGGAGGCGGGAGAGGAAGAGGGGGAAGACGGAGACGCCTTTGTGACGGAGG GGAGGGCACCATGGAGGAGGCGGGAGAGGAAG_GGGGGAAGACGGAGACGCCTTTGTGACGGAGG GA G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228360026..228360257 26863196 MeRIP-seq:(Medium) rs1558396142 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_267772,RMVar_hsa_circ_324283 86194 RMVar_ID_86194 Human_SNP_ID_52607403 m1A Human chr1 - 228401082 228401082 228401082 GCTGCTGCAGAGGCTGGAGGAGGAGGAGCTGGAGGTGCTGCCCCGGCTGCGGGAGGGCGCAGCCC GCTGCTGCAGAGGCTGGAGGAGGAGGAGCTGGGGGTGCTGCCCCGGCTGCGGGAGGGCGCAGCCC T C TRIM11 Ensembl:ENSG00000154370 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228401031..228401228 26863196 MeRIP-seq:(Medium) rs1235990280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222434,Human_RBP_ID_802103,Human_RBP_ID_850960,Human_RBP_ID_5334253,Human_RBP_ID_8755416,Human_RBP_ID_9319424,Human_RBP_ID_18969701 Human_miRNA_ID_2014788 RMVar_hsa_circ_116416,RMVar_hsa_circ_122104,RMVar_hsa_circ_140247,RMVar_hsa_circ_112757,RMVar_hsa_circ_140245,RMVar_hsa_circ_140246,RMVar_hsa_circ_118557,RMVar_hsa_circ_292509,RMVar_hsa_circ_140251,RMVar_hsa_circ_326791 86195 RMVar_ID_86195 Human_SNP_ID_52607551 m1A Human chr1 - 228401584 228401584 228401584 AGGAGGGACCCTGGGTGGTAGATTTGTAGTCCAGCTGGCCCCAGGTGGTAGATGCAGGGTTCTAC AGGAGGGACCCTGGGTGGTAGATTTGTAGTCCGGCTGGCCCCAGGTGGTAGATGCAGGGTTCTAC T C TRIM11 Ensembl:ENSG00000154370 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228401582..228401686 26863196 MeRIP-seq:(Medium) rs1446967743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9411422,Human_RBP_ID_10825272,Human_RBP_ID_22561554 RMVar_hsa_circ_122104,RMVar_hsa_circ_112757,RMVar_hsa_circ_140245,RMVar_hsa_circ_140246,RMVar_hsa_circ_118557,RMVar_hsa_circ_292509,RMVar_hsa_circ_140251,RMVar_hsa_circ_326791 86196 RMVar_ID_86196 Human_SNP_ID_52607786 m1A Human chr1 - 228402432 228402432 228402432 GAACCCTTGAGGTAGCTTTGCAAAGGGGGGTGAGGCCTGGGCTAGGGTAGCAAGGTCGAGGACTA GAACCCTTGAGGTAGCTTTGCAAAGGGGGGTGGGGCCTGGGCTAGGGTAGCAAGGTCGAGGACTA T C TRIM11 Ensembl:ENSG00000154370 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:228402337..228402533 26863196 MeRIP-seq:(Medium) rs61827274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5334254,Human_RBP_ID_5774056 RMVar_hsa_circ_122104,RMVar_hsa_circ_140245 86197 RMVar_ID_86197 Human_SNP_ID_52608824 m1A Human chr1 - 228406593 228406593 228406593 AGCTGCCGAGGCCGCCCGCCGCCGCCCCGCGGACAGTACCGCCTTCCTCCCCTCTGTCCGCGCCA AGCTGCCGAGGCCGCCCGCCGCCGCCCCGCGGGCAGTACCGCCTTCCTCCCCTCTGTCCGCGCCA T C TRIM11 Ensembl:ENSG00000154370 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228406543..228406802 26863196 MeRIP-seq:(Medium) rs766089849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4030276,Human_RBP_ID_9320397,Human_RBP_ID_22427854 Human_miRNA_ID_3076471 RMVar_hsa_circ_122104,RMVar_hsa_circ_140245 86198 RMVar_ID_86198 Human_SNP_ID_52608833 m1A Human chr1 + 228406622 228406622 228406622 CTGTCCGCGGGGCGGCGGCGGGCGGCCTCGGCAGCTCGCGGGGACGCGGGGTATCCGGGTGCGGC CTGTCCGCGGGGCGGCGGCGGGCGGCCTCGGCGGCTCGCGGGGACGCGGGGTATCCGGGTGCGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:228406581..228406759 26863196 MeRIP-seq:(Medium) rs1360006052 Functional Loss SNV dbSNP153 33..33 33 - - - 86199 RMVar_ID_86199 Human_SNP_ID_52608837 m1A Human chr1 - 228406641 228406641 228406641 GAGTGCCCGAGCCTGCGCCGCCGCACCCGGATACCCCGCGTCCCCGCGAGCTGCCGAGGCCGCCC GAGTGCCCGAGCCTGCGCCGCCGCACCCGGATCCCCCGCGTCCCCGCGAGCTGCCGAGGCCGCCC T G TRIM11 Ensembl:ENSG00000154370 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:228406476..228406825 26863410 MeRIP-seq:(Medium) rs930627673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4030278,Human_RBP_ID_5338997,Human_RBP_ID_9320397 RMVar_hsa_circ_122104,RMVar_hsa_circ_140245 86200 RMVar_ID_86200 Human_SNP_ID_52608840 m1A Human chr1 - 228406649 228406649 228406649 GCGCCCCGGAGTGCCCGAGCCTGCGCCGCCGCACCCGGATACCCCGCGTCCCCGCGAGCTGCCGA GCGCCCCGGAGTGCCCGAGCCTGCGCCGCCGCCCCCGGATACCCCGCGTCCCCGCGAGCTGCCGA T G TRIM11 Ensembl:ENSG00000154370 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:228406551..228406800 26863410 MeRIP-seq:(Medium) rs941519706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5338997,Human_RBP_ID_9320397 RMVar_hsa_circ_122104,RMVar_hsa_circ_140245 86201 RMVar_ID_86201 Human_SNP_ID_52611846 m1A Human chr1 + 228416718 228416718 228416718 TGGCGTCAGCGGGGGCTGGGGGGCGGCGGGGGAGGGGAATGCTGGGCGAGGGAGTGTTCGGCGGC TGGCGTCAGCGGGGGCTGGGGGGCGGCGGGGGGGGGGAATGCTGGGCGAGGGAGTGTTCGGCGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228416460..228416871 26863196 MeRIP-seq:(Medium) rs1378078307 Functional Loss SNV dbSNP153 33..33 33 - - - 86202 RMVar_ID_86202 Human_SNP_ID_52611862 m1A Human chr1 - 228416782 228416782 228416782 CCCCTGCCGCCTTCCTTCCCCAAGCCACCCCCAACCTCTCCTAAGAGGCGCCGCCCCAGTCCCGG CCCCTGCCGCCTTCCTTCCCCAAGCCACCCCCCACCTCTCCTAAGAGGCGCCGCCCCAGTCCCGG T G TRIM17 Ensembl:ENSG00000162931 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228416732..228416915 26863196 MeRIP-seq:(Medium) rs1391479005 Functional Loss SNV dbSNP153 33..33 33 - - - 86203 RMVar_ID_86203 Human_SNP_ID_52611867 m1A Human chr1 - 228416793 228416793 228416793 GAGCCTTCCACCCCCTGCCGCCTTCCTTCCCCAAGCCACCCCCAACCTCTCCTAAGAGGCGCCGC GAGCCTTCCACCCCCTGCCGCCTTCCTTCCCCCAGCCACCCCCAACCTCTCCTAAGAGGCGCCGC T G TRIM17 Ensembl:ENSG00000162931 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228416746..228416892 26863196 MeRIP-seq:(Medium) rs1373101361 Functional Loss SNV dbSNP153 33..33 33 - - - 86204 RMVar_ID_86204 Human_SNP_ID_52611965 m1A Human chr1 - 228417120 228417119 228417120 CCCCTACCCCGACCAACTTAGCCCCTCACCTAACCCTCCAGCCTGGGGCTCGCGTGCCCTCCCGC CCCCTACCCCGACCAACTTAGCCCCTCACCTA_CCCTCCAGCCTGGGGCTCGCGTGCCCTCCCGC GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228417088..228417249 26863196 MeRIP-seq:(Medium) rs1394835092 Functional Loss DEL dbSNP153 33..33 33 - - - 86205 RMVar_ID_86205 Human_SNP_ID_52622645 m1A Human chr1 + 228458382 228458379 228458382 TCGCCAGCGAGGCCTCCCGCCTGGCACACTACAACAAGCGCTCCACCATCACGTCCCGCGAAGTG TCGCCAGCGAGGCCTCCCGCCTGGCACACT___ACAAGCGCTCCACCATCACGTCCCGCGAAGTG TACA T H2BU1 Ensembl:ENSG00000196890 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:228458181..228458464 26863196 MeRIP-seq:(Medium) rs754975292 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_272451,Human_RBP_ID_5433682,Human_RBP_ID_5457166,Human_RBP_ID_8744571,Human_RBP_ID_17216367,Human_RBP_ID_17333840,Human_RBP_ID_17450548,Human_RBP_ID_17741889,Human_RBP_ID_18187396,Human_RBP_ID_26376519,Human_RBP_ID_26799549,Human_RBP_ID_26855882,Human_RBP_ID_27177365 86206 RMVar_ID_86206 Human_SNP_ID_52630559 m1A Human chr1 - 228487500 228487500 228487500 CACAGGGCGCAGGCGGCCTCGGCGGGGCCCGCAGGGAGCGCCAGGGCTGCGGGCGGCGGGGCCGG CACAGGGCGCAGGCGGCCTCGGCGGGGCCCGCCGGGAGCGCCAGGGCTGCGGGCGGCGGGGCCGG T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:228487415..228487499 26863410 MeRIP-seq:(Medium) rs1328047211 Functional Loss SNV dbSNP153 33..33 33 - - - 86207 RMVar_ID_86207 Human_SNP_ID_52631100 m1A Human chr1 + 228488989 228488989 228488989 CAGGAGAACAAGGGGTCTGTGGAAATCATGAGAAAGGACTTGAATGACGCCCGGGACCTGCATGG CAGGAGAACAAGGGGTCTGTGGAAATCATGAGCAAGGACTTGAATGACGCCCGGGACCTGCATGG A C RNF187 Ensembl:ENSG00000168159 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:228488951..228489050 26863196 MeRIP-seq:(Medium) rs1324386246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423244,Human_RBP_ID_1739345,Human_RBP_ID_3301026,Human_RBP_ID_4090507,Human_RBP_ID_5162215,Human_RBP_ID_8301420,Human_RBP_ID_10825624,Human_RBP_ID_23370956 Human_Splice_Rec_197092,Human_Splice_Rec_197096,Human_Splice_Rec_197097 86208 RMVar_ID_86208 Human_SNP_ID_52631110 m1A Human chr1 + 228489028 228489027 228489029 TTGAATGACGCCCGGGACCTGCATGGCCAGGCAGAGTCAGCAGCTGCAGTGTGGAAGGCAAGTGG TTGAATGACGCCCGGGACCTGCATGGCCAGGC__AGTCAGCAGCTGCAGTGTGGAAGGCAAGTGG CAG C RNF187 Ensembl:ENSG00000168159 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:228488951..228489100;chr1:228488951..228489120;chr1:228488951..228489117;chr1:228488951..228489075 26863196,32194978 MeRIP-seq:(Medium) rs771234504 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_224519,Human_RBP_ID_5234107,Human_RBP_ID_17338696,Human_RBP_ID_22427861,Human_RBP_ID_26387000 Human_Splice_Rec_197092,Human_Splice_Rec_197096,Human_Splice_Rec_197097 Human_miRNA_ID_203600,Human_miRNA_ID_1488699 86209 RMVar_ID_86209 Human_SNP_ID_52632576 m1A Human chr1 - 228493886 228493886 228493886 CTCCAGCTCTGGGACTGCCACGGGTTGGCGCCATCACTGCATGGGAGGGGAGAGGGAAAGACAGA CTCCAGCTCTGGGACTGCCACGGGTTGGCGCCGTCACTGCATGGGAGGGGAGAGGGAAAGACAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228493876..228493925 26863196 MeRIP-seq:(Medium) rs1477063397 Functional Loss SNV dbSNP153 33..33 33 - - - 86210 RMVar_ID_86210 Human_SNP_ID_52632735 m1A Human chr1 - 228494426 228494424 228494426 GGATAAGGCTGGGCCGGGCCCACGCCCACCTCAAGAGGGGGGCCGCCTCCTCAGGAGGCATCAAG GGATAAGGCTGGGCCGGGCCCACGCCCACCTC__GAGGGGGGCCGCCTCCTCAGGAGGCATCAAG CTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228494376..228494650 32194978 MeRIP-seq:(Medium) rs1436010305 Functional Loss DEL dbSNP153 33..34 33 - - - 86211 RMVar_ID_86211 Human_SNP_ID_52632735 m1A Human chr1 - 228494425 228494424 228494426 GATAAGGCTGGGCCGGGCCCACGCCCACCTCAAGAGGGGGGCCGCCTCCTCAGGAGGCATCAAGG GATAAGGCTGGGCCGGGCCCACGCCCACCTC__GAGGGGGGCCGCCTCCTCAGGAGGCATCAAGG CTT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:228494376..228494675 26863196 MeRIP-seq:(Medium) rs1436010305 Functional Loss DEL dbSNP153 32..33 33 - - - 86212 RMVar_ID_86212 Human_SNP_ID_52633057 m1A Human chr1 + 228495438 228495438 228495438 AGGGCAAAGAGGGCCCTAGGAGAAGATTCCAGAGCCTGGCCAGAGTTTGGCCAAGTAGAGAATCT AGGGCAAAGAGGGCCCTAGGAGAAGATTCCAGGGCCTGGCCAGAGTTTGGCCAAGTAGAGAATCT A G RNF187 Ensembl:ENSG00000168159 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10916331 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10324,GWAS_ID_10325,GWAS_ID_10326 86213 RMVar_ID_86213 Human_SNP_ID_52650308 m1A Human chr1 + 228621067 228621067 228621067 GTAAAGGCGGAGCAGAGTCAGGGGAGGTTGGGAAGCATGGCGACTGTGGGGGGAAGGGAGGCAGC GTAAAGGCGGAGCAGAGTCAGGGGAGGTTGGGTAGCATGGCGACTGTGGGGGGAAGGGAGGCAGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:228621029..228621188;chr1:228620936..228621125;chr1:228621006..228621110;chr1:228620993..228621114 26863196 MeRIP-seq:(Medium) rs1209734778 Functional Loss SNV dbSNP153 33..33 33 - - - 86214 RMVar_ID_86214 Human_SNP_ID_52652153 m1A Human chr1 + 228635618 228635618 228635618 GCGCGCTCGCACGCGCGCGCGCGGACACACACACACACAGACACACACGCACACACGCACGCGCA GCGCGCTCGCACGCGCGCGCGCGGACACACACGCACACAGACACACACGCACACACGCACGCGCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr1:228635551..228635650;chr1:228635576..228635650;chr1:228635513..228635701 26863196 MeRIP-seq:(Medium) rs199818102 Functional Loss SNV dbSNP153 33..33 33 - - - 86215 RMVar_ID_86215 Human_SNP_ID_52652158 m1A Human chr1 + 228635622 228635622 228635622 GCTCGCACGCGCGCGCGCGGACACACACACACACAGACACACACGCACACACGCACGCGCACACG GCTCGCACGCGCGCGCGCGGACACACACACACGCAGACACACACGCACACACGCACGCGCACACG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228635577..228635671 26863196 MeRIP-seq:(Medium) rs1425911844 Functional Loss SNV dbSNP153 33..33 33 - - - 86216 RMVar_ID_86216 Human_SNP_ID_52653106 m1A Human chr1 + 228646878 228646869 228646879 GGAGAGCAAGGAGAAGATGGATGGAGAGATAGAAACCGAGGGAGGGAGAGAGACAGCGATCGAGA GGAGAGCAAGGAGAAGATGGATGG__________ACCGAGGGAGGGAGAGAGACAGCGATCGAGA GAGAGATAGAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228646832..228647109 26863196 MeRIP-seq:(Medium) rs1424581828 Functional Loss DEL dbSNP153 25..34 33 - - - 86217 RMVar_ID_86217 Human_SNP_ID_52653107 m1A Human chr1 + 228646870 228646870 228646870 GGCTTGAAGGAGAGCAAGGAGAAGATGGATGGAGAGATAGAAACCGAGGGAGGGAGAGAGACAGC GGCTTGAAGGAGAGCAAGGAGAAGATGGATGGCGAGATAGAAACCGAGGGAGGGAGAGAGACAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228646801..228647234 26863196 MeRIP-seq:(Medium) rs529124657 Functional Loss SNV dbSNP153 33..33 33 - - - 86218 RMVar_ID_86218 Human_SNP_ID_52653108 m1A Human chr1 + 228646870 228646870 228646870 GGCTTGAAGGAGAGCAAGGAGAAGATGGATGGAGAGATAGAAACCGAGGGAGGGAGAGAGACAGC GGCTTGAAGGAGAGCAAGGAGAAGATGGATGGGGAGATAGAAACCGAGGGAGGGAGAGAGACAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228646801..228647234 26863196 MeRIP-seq:(Medium) rs529124657 Functional Loss SNV dbSNP153 33..33 33 - - - 86219 RMVar_ID_86219 Human_SNP_ID_52653117 m1A Human chr1 + 228646878 228646878 228646878 GGAGAGCAAGGAGAAGATGGATGGAGAGATAGAAACCGAGGGAGGGAGAGAGACAGCGATCGAGA GGAGAGCAAGGAGAAGATGGATGGAGAGATAGTAACCGAGGGAGGGAGAGAGACAGCGATCGAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:228646832..228647109 26863196 MeRIP-seq:(Medium) rs1235241579 Functional Loss SNV dbSNP153 33..33 33 - - - 86220 RMVar_ID_86220 Human_SNP_ID_52653137 m1A Human chr1 + 228646900 228646900 228646900 GGAGAGATAGAAACCGAGGGAGGGAGAGAGACAGCGATCGAGAGAGACCGGAGAGGTGGAGAGGT GGAGAGATAGAAACCGAGGGAGGGAGAGAGACCGCGATCGAGAGAGACCGGAGAGGTGGAGAGGT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:228646862..228646993 26863196 MeRIP-seq:(Medium) rs551822662 Functional Loss SNV dbSNP153 33..33 33 - - - 86221 RMVar_ID_86221 Human_SNP_ID_52653160 m1A Human chr1 + 228646919 228646919 228646919 GAGGGAGAGAGACAGCGATCGAGAGAGACCGGAGAGGTGGAGAGGTAAAGAGAGAGAGGCTAAGA GAGGGAGAGAGACAGCGATCGAGAGAGACCGGGGAGGTGGAGAGGTAAAGAGAGAGAGGCTAAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:228646752..228647205;chr1:228646812..228647195 26863196 MeRIP-seq:(Medium) rs377316774 Functional Loss SNV dbSNP153 33..33 33 - - - 86222 RMVar_ID_86222 Human_SNP_ID_52653771 m1A Human chr1 - 228647822 228647822 228647822 ACCGTAAATCTGCTCCCTCTTTTCACACGCCCAAGCCCACACAACAGCCCGGGACCGCTTAGTGT ACCGTAAATCTGCTCCCTCTTTTCACACGCCCGAGCCCACACAACAGCCCGGGACCGCTTAGTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228647774..228647892 26863196 MeRIP-seq:(Medium) rs1260366142 Functional Loss SNV dbSNP153 33..33 33 - - - 86223 RMVar_ID_86223 Human_SNP_ID_52803498 m1A Human chr1 + 229271202 229271176 229271202 CTGGAGTCCGGCTGGGCCGCAGCCGCTGGGAGACCGGCGGTTGCCGTGGGGACCGGTCGGGCCCC CTGGAGT__________________________CCGGCGGTTGCCGTGGGGACCGGTCGGGCCCC TCCGGCTGGGCCGCAGCCGCTGGGAGA T RAB4A Ensembl:ENSG00000168118 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:229271151..229271350 26863196 MeRIP-seq:(Medium) rs1380327774 Functional Loss DEL dbSNP153 8..33 33 - - - Human_RBP_ID_224514,Human_RBP_ID_4073311,Human_RBP_ID_5457187,Human_RBP_ID_5485636,Human_RBP_ID_17742067,Human_RBP_ID_18415726 86224 RMVar_ID_86224 Human_SNP_ID_52807643 m1A Human chr1 + 229288783 229288783 229288783 AATAGGAGTGGAATTTGGTTCAAAGATAATAAATGTTGGTGGTAAATATGTAAAGTTACAAATAT AATAGGAGTGGAATTTGGTTCAAAGATAATAACTGTTGGTGGTAAATATGTAAAGTTACAAATAT A C RAB4A Ensembl:ENSG00000168118 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:229288732..229288881 32194978 MeRIP-seq:(Medium) rs1314499748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1739379,Human_RBP_ID_3301115,Human_RBP_ID_27589094 Human_Splice_Rec_197176,Human_Splice_Rec_197180,Human_Splice_Rec_197181,Human_Splice_Rec_197198,Human_Splice_Rec_197199 Human_miRNA_ID_1712820 RMVar_hsa_circ_140254,RMVar_hsa_circ_349871,RMVar_hsa_circ_358081,RMVar_hsa_circ_140255,RMVar_hsa_circ_140256 86225 RMVar_ID_86225 Human_SNP_ID_52808834 m1A Human chr1 + 229293677 229293677 229293677 CCTGCCCCATGGAGGGGAGGCAGGCAGCCAACACAGAGACAGAGACAGAAAGAGCATCCCACCAA CCTGCCCCATGGAGGGGAGGCAGGCAGCCAACGCAGAGACAGAGACAGAAAGAGCATCCCACCAA A G RAB4A Ensembl:ENSG00000168118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:229293671..229294026 26863196 MeRIP-seq:(Medium) rs919794843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140254,RMVar_hsa_circ_358081,RMVar_hsa_circ_140255,RMVar_hsa_circ_140256 86226 RMVar_ID_86226 Human_SNP_ID_52809019 m1A Human chr1 - 229294373 229294373 229294373 ACTCGCGCAGCCTCTGCGCCCTGCACTCTGCTAGTCTTCCTCCCGCTCACCAGCCACTTCTCTGG ACTCGCGCAGCCTCTGCGCCCTGCACTCTGCTCGTCTTCCTCCCGCTCACCAGCCACTTCTCTGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:229294365..229294480 26863196 MeRIP-seq:(Medium) rs1367773635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140257 86227 RMVar_ID_86227 Human_SNP_ID_52809825 m1A Human chr1 - 229297532 229297532 229297532 CACAAAGGATGATCACAATGTTCTGGCTCGCTAGCATTCGGGCATCTGTTAACCAATTAGTAAGC CACAAAGGATGATCACAATGTTCTGGCTCGCTGGCATTCGGGCATCTGTTAACCAATTAGTAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:229297447..229297550 26863196 MeRIP-seq:(Medium) rs752249758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140257 86228 RMVar_ID_86228 Human_SNP_ID_52811294 m1A Human chr1 + 229302905 229302905 229302905 CCAGAAAGAATGGGCTCAGGTATTCAGTACGGAGATGCTGCCTTGAGACAGCTGAGGTCACCGCG CCAGAAAGAATGGGCTCAGGTATTCAGTACGGGGATGCTGCCTTGAGACAGCTGAGGTCACCGCG A G RAB4A Ensembl:ENSG00000168118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:229299066..229303000 26863196 MeRIP-seq:(Medium) rs1161449155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_344953,Human_RBP_ID_1423313,Human_RBP_ID_1739388,Human_RBP_ID_4030656,Human_RBP_ID_5774576,Human_RBP_ID_8964472,Human_RBP_ID_10826574,Human_RBP_ID_23371148 Human_Splice_Rec_197170,Human_Splice_Rec_197171,Human_Splice_Rec_197186,Human_Splice_Rec_197187,Human_Splice_Rec_197194,Human_Splice_Rec_197195 Human_miRNA_ID_39819,Human_miRNA_ID_68539 RMVar_hsa_circ_140254,RMVar_hsa_circ_358081,RMVar_hsa_circ_140255,RMVar_hsa_circ_140256,RMVar_hsa_circ_140258 86229 RMVar_ID_86229 Human_SNP_ID_52820821 m1A Human chr1 - 229342504 229342504 229342504 GTGTCGTGTACCGGGTCCCGTAGGCTGCGGGCAGCGAGGAGCGGCTGGCGCTCGAGGCGGCGGAC GTGTCGTGTACCGGGTCCCGTAGGCTGCGGGCGGCGAGGAGCGGCTGGCGCTCGAGGCGGCGGAC T C CCSAP Ensembl:ENSG00000154429 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:229342069..229342946;chr1:229342056..229343005 26863196 MeRIP-seq:(Medium) rs1191110830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224259,Human_RBP_ID_745203,Human_RBP_ID_5086269,Human_RBP_ID_5312893,Human_RBP_ID_9319437,Human_RBP_ID_18969703,Human_RBP_ID_22871078,Human_RBP_ID_26312874,Human_RBP_ID_27801649 Human_Splice_Rec_197208,Human_Splice_Rec_197218 86230 RMVar_ID_86230 Human_SNP_ID_52844546 m1A Human chr1 - 229431626 229431626 229431626 ACGCGCTGTCTTGCAGATCATCGCCCCGCCGGAGCGCAAATACTCGGTGTGGATCGGCGGCTCCA ACGCGCTGTCTTGCAGATCATCGCCCCGCCGGGGCGCAAATACTCGGTGTGGATCGGCGGCTCCA T C ACTA1 Ensembl:ENSG00000143632 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:229431580..229431707 26863196 MeRIP-seq:(Medium) rs121909528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_197234,Human_Splice_Rec_197242 Clinvar_Rec_457 GWAS_ID_10327 86231 RMVar_ID_86231 Human_SNP_ID_52844547 m1A Human chr1 - 229431626 229431626 229431626 ACGCGCTGTCTTGCAGATCATCGCCCCGCCGGAGCGCAAATACTCGGTGTGGATCGGCGGCTCCA ACGCGCTGTCTTGCAGATCATCGCCCCGCCGGCGCGCAAATACTCGGTGTGGATCGGCGGCTCCA T G ACTA1 Ensembl:ENSG00000143632 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:229431580..229431707 26863196 MeRIP-seq:(Medium) rs121909528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_197234,Human_Splice_Rec_197242 Clinvar_Rec_457 GWAS_ID_10327 86232 RMVar_ID_86232 Human_SNP_ID_52875435 m1A Human chr1 + 229551234 229551232 229551234 AAAAATTGCTCTTGCCCCTCCTTAAGGTCTTTATAAAGTCCCCTCCCCAAAAAGGCCTGCTCTGA AAAAATTGCTCTTGCCCCTCCTTAAGGTCTT__TAAAGTCCCCTCCCCAAAAAGGCCTGCTCTGA TTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:229551232..229551311 26863196 MeRIP-seq:(Medium) rs1272015032 Functional Loss DEL dbSNP153 32..33 33 - - - 86233 RMVar_ID_86233 Human_SNP_ID_52877343 m1A Human chr1 - 229558652 229558652 229558652 CGGGCTGAGGCGTACGGGTCGCACGCAGCGCCATGCGAGGCCCCCCTGCCTGGCCGCTGCGGCTG CGGGCTGAGGCGTACGGGTCGCACGCAGCGCCTTGCGAGGCCCCCCTGCCTGGCCGCTGCGGCTG T A ABCB10 Ensembl:ENSG00000135776 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:229558551..229558724 26863410 MeRIP-seq:(Medium) rs1396033841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4031081,Human_RBP_ID_8755430,Human_RBP_ID_9319442,Human_RBP_ID_22428827 86234 RMVar_ID_86234 Human_SNP_ID_52877447 m1A Human chr1 - 229558832 229558832 229558832 GTGGGGCGGAGAGGCGCGGCACCGCGCGGACGAGGATGGGGCGGGGGCGGGCGCAGCCCGAGGGT GTGGGGCGGAGAGGCGCGGCACCGCGCGGACGGGGATGGGGCGGGGGCGGGCGCAGCCCGAGGGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:229558597..229558925 26863196 MeRIP-seq:(Medium) rs1558132222 Functional Loss SNV dbSNP153 33..33 33 - - - 86235 RMVar_ID_86235 Human_SNP_ID_52891349 m1A Human chr1 - 229614474 229614474 229614474 CTGTCGTTGCCTCCCTTGAAGGTCATGAAACGAGTGCGTACCGAGCAGATTCAGATGGCAGTGTC CTGTCGTTGCCTCCCTTGAAGGTCATGAAACGGGTGCGTACCGAGCAGATTCAGATGGCAGTGTC T C TAF5L Ensembl:ENSG00000135801 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:229614399..229626047 26863196 MeRIP-seq:(Medium) rs1260415887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_860939,Human_RBP_ID_4074835 Human_Splice_Rec_197356,Human_Splice_Rec_197364,Human_Splice_Rec_197370,Human_Splice_Rec_197378 Human_miRNA_ID_2589883,Human_miRNA_ID_2589884 RMVar_hsa_circ_114915,RMVar_hsa_circ_116953,RMVar_hsa_circ_140339,RMVar_hsa_circ_140340,RMVar_hsa_circ_111470,RMVar_hsa_circ_292872,RMVar_hsa_circ_348090,RMVar_hsa_circ_140341,RMVar_hsa_circ_140342 86236 RMVar_ID_86236 Human_SNP_ID_52894401 m1A Human chr1 + 229626277 229626244 229626278 CCGTACAGCGGCCTCCGCCGCACCGGGACAGCAGCCGCCGCCGCTGCCGCCGTCCTCCCCTGTCT __________________________________CCGCCGCCGCTGCCGCCGTCCTCCCCTGTCT CCCGTACAGCGGCCTCCGCCGCACCGGGACAGCAG C URB2 Ensembl:ENSG00000135763 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:229626232..229626320 26863196 MeRIP-seq:(Medium) rs1304860637 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_4074836 Human_Splice_Rec_197379 RMVar_hsa_circ_79586,RMVar_hsa_circ_140343 86237 RMVar_ID_86237 Human_SNP_ID_52894425 m1A Human chr1 + 229626272 229626272 229626272 GGGACCCGTACAGCGGCCTCCGCCGCACCGGGACAGCAGCCGCCGCCGCTGCCGCCGTCCTCCCC GGGACCCGTACAGCGGCCTCCGCCGCACCGGGCCAGCAGCCGCCGCCGCTGCCGCCGTCCTCCCC A C URB2 Ensembl:ENSG00000135763 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:229626221..229626348 26863196 MeRIP-seq:(Medium) rs999799177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074836 Human_Splice_Rec_197379 RMVar_hsa_circ_79586,RMVar_hsa_circ_140343 86238 RMVar_ID_86238 Human_SNP_ID_52894430 m1A Human chr1 + 229626277 229626277 229626277 CCGTACAGCGGCCTCCGCCGCACCGGGACAGCAGCCGCCGCCGCTGCCGCCGTCCTCCCCTGTCT CCGTACAGCGGCCTCCGCCGCACCGGGACAGCCGCCGCCGCCGCTGCCGCCGTCCTCCCCTGTCT A C URB2 Ensembl:ENSG00000135763 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:229626232..229626320 26863196 MeRIP-seq:(Medium) rs867958111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074836 Human_Splice_Rec_197379 RMVar_hsa_circ_79586,RMVar_hsa_circ_140343 86239 RMVar_ID_86239 Human_SNP_ID_52904747 m1A Human chr1 - 229664900 229664900 229664900 GATAGTCGAGGCCCTAGAGGATGCAGAGAGCCAGCGGGGGGTCCGACCAGCCAAGGGTGTCCAGC GATAGTCGAGGCCCTAGAGGATGCAGAGAGCCGGCGGGGGGTCCGACCAGCCAAGGGTGTCCAGC T C lnc-TAF5L-4,lnc-TAF5L-4:2 RNACentral:URS00008B399F,RNACentral:URS00008B900D lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:229664849..229664927 26863196 MeRIP-seq:(Medium) rs890439760 Functional Loss SNV dbSNP153 33..33 33 - - - 86240 RMVar_ID_86240 Human_SNP_ID_53004619 m1A Human chr1 - 230067367 230067367 230067367 CCGGCGCCGCCGCCCGCGCCCCCGGCCAGCGCAGAGCCGCCCCCCGAGTACATGTAGTAGGCGAT CCGGCGCCGCCGCCCGCGCCCCCGGCCAGCGCGGAGCCGCCCCCCGAGTACATGTAGTAGGCGAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:230067326..230067400 26863196 MeRIP-seq:(Medium) rs1489545398 Functional Loss SNV dbSNP153 33..33 33 - - - 86241 RMVar_ID_86241 Human_SNP_ID_53008560 m1A Human chr1 + 230082792 230082792 230082792 GGGATCCAGGCTGATACATCAGGGGAACTTGCAGAGAGAATAGGGGATCCAGGATGATAGAGCAG GGGATCCAGGCTGATACATCAGGGGAACTTGCGGAGAGAATAGGGGATCCAGGATGATAGAGCAG A G GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:230082786..230083582;chr1:230082786..230083583 26863196 MeRIP-seq:(Medium) rs1229441284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2129018,Human_RBP_ID_10832238 86242 RMVar_ID_86242 Human_SNP_ID_53008561 m1A Human chr1 + 230082792 230082792 230082792 GGGATCCAGGCTGATACATCAGGGGAACTTGCAGAGAGAATAGGGGATCCAGGATGATAGAGCAG GGGATCCAGGCTGATACATCAGGGGAACTTGCTGAGAGAATAGGGGATCCAGGATGATAGAGCAG A T GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:230082786..230083582;chr1:230082786..230083583 26863196 MeRIP-seq:(Medium) rs1229441284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2129018,Human_RBP_ID_10832238 86243 RMVar_ID_86243 Human_SNP_ID_53008993 m1A Human chr1 + 230084180 230084178 230084180 CCAGCACAGGCTTGGCCCCTCCCACAGCAGGGAGACAGTGGGGAGCCAGGCTAACATGGGCCCAG CCAGCACAGGCTTGGCCCCTCCCACAGCAGG__GACAGTGGGGAGCCAGGCTAACATGGGCCCAG GGA G GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:230084176..230084545;chr1:230084175..230084447 26863196 MeRIP-seq:(Medium) rs1221059911 Functional Loss DEL dbSNP153 32..33 33 - - - 86244 RMVar_ID_86244 Human_SNP_ID_53009006 m1A Human chr1 + 230084232 230084232 230084232 AACATGGGCCCAGGGATGTATATTCTGGAAGGAGGGCAGGCTGGGGGACGGTCACGCCAATATCA AACATGGGCCCAGGGATGTATATTCTGGAAGGTGGGCAGGCTGGGGGACGGTCACGCCAATATCA A T GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:230084228..230084561 26863196 MeRIP-seq:(Medium) rs960604480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800727,Human_RBP_ID_5776293,Human_RBP_ID_8051961,Human_RBP_ID_18474404 86245 RMVar_ID_86245 Human_SNP_ID_53040392 m1A Human chr1 - 230208405 230208405 230208405 TTAACATGTCCACATTTCCCTACACCTGCTCCACTCACAGCCTCCCTATATCTCAGCTGAGGAGA TTAACATGTCCACATTTCCCTACACCTGCTCCTCTCACAGCCTCCCTATATCTCAGCTGAGGAGA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:230208279..230208408 26863196 MeRIP-seq:(Medium) rs1427498823 Functional Loss SNV dbSNP153 33..33 33 - - - 86246 RMVar_ID_86246 Human_SNP_ID_53047242 m1A Human chr1 + 230236724 230236724 230236724 AAAGTGCGAGTTCTTAGAAATGATCGACGAGAAGGTAAGATTCTTCTTAATTCAGCGCCAAGACA AAAGTGCGAGTTCTTAGAAATGATCGACGAGACGGTAAGATTCTTCTTAATTCAGCGCCAAGACA A C GALNT2 Ensembl:ENSG00000143641 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230236701..230236750 26863196 MeRIP-seq:(Medium) rs1438859528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24450864 Human_Splice_Rec_197468,Human_Splice_Rec_197469,Human_Splice_Rec_197480,Human_Splice_Rec_197481 RMVar_hsa_circ_55429,RMVar_hsa_circ_361088,RMVar_hsa_circ_340437,RMVar_hsa_circ_72993,RMVar_hsa_circ_25884,RMVar_hsa_circ_140351,RMVar_hsa_circ_140355,RMVar_hsa_circ_289117,RMVar_hsa_circ_300936,RMVar_hsa_circ_336011,RMVar_hsa_circ_140356,RMVar_hsa_circ_140357,RMVar_hsa_circ_80205,RMVar_hsa_circ_315336,RMVar_hsa_circ_375741,RMVar_hsa_circ_267901,RMVar_hsa_circ_140358 86247 RMVar_ID_86247 Human_SNP_ID_53056872 m1A Human chr1 - 230274429 230274429 230274429 TTCGTCAAGGCCCATTCCTGGAACACAAAACCAGAAGTCAGAGGCGTGCTATGCACCGGGCTGTG TTCGTCAAGGCCCATTCCTGGAACACAAAACCGGAAGTCAGAGGCGTGCTATGCACCGGGCTGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230274426..230274525 26863196 MeRIP-seq:(Medium) rs199598467 Functional Loss SNV dbSNP153 33..33 33 - - - 86248 RMVar_ID_86248 Human_SNP_ID_53056931 m1A Human chr1 + 230274563 230274563 230274563 GCTGCAGGGCTGCCGAGAAAATGACAGCAGACAGGTACGGCTTGCAGGCACCCGTGGGTGCCCGT GCTGCAGGGCTGCCGAGAAAATGACAGCAGACGGGTACGGCTTGCAGGCACCCGTGGGTGCCCGT A G GALNT2 Ensembl:ENSG00000143641 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:230274538..230279427 32194978 MeRIP-seq:(Medium) rs544481491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9343281,Human_RBP_ID_19040416,Human_RBP_ID_26387031 Human_Splice_Rec_197499,Human_Splice_Rec_197511 RMVar_hsa_circ_140357,RMVar_hsa_circ_80205,RMVar_hsa_circ_118949,RMVar_hsa_circ_140368,RMVar_hsa_circ_42423,RMVar_hsa_circ_320443 86249 RMVar_ID_86249 Human_SNP_ID_53058654 m1A Human chr1 + 230279626 230279626 230279626 CTTCGGCAAGGCACGGACGACTGTGCAGACACAGCAGCGGCAAGAAGCGAGAACTGCCCTCCCCC CTTCGGCAAGGCACGGACGACTGTGCAGACACGGCAGCGGCAAGAAGCGAGAACTGCCCTCCCCC A G GALNT2 Ensembl:ENSG00000143641 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:230279576..230279876 32194978 MeRIP-seq:(Medium) rs146911682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17223594,Human_RBP_ID_17456595,Human_RBP_ID_24450891,Human_RBP_ID_27177726 86250 RMVar_ID_86250 Human_SNP_ID_53059099 m1A Human chr1 + 230281052 230281052 230281052 AGAGAGGCTGGCACGGCCTGGCAGTCTGAGAAAAGCGTCAGTTAGGCACACCTGCAGGCCCCTCG AGAGAGGCTGGCACGGCCTGGCAGTCTGAGAAGAGCGTCAGTTAGGCACACCTGCAGGCCCCTCG A G GALNT2 Ensembl:ENSG00000143641 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230281005..230281170 26863196 MeRIP-seq:(Medium) rs1469123513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101635,Human_RBP_ID_24450905 86251 RMVar_ID_86251 Human_SNP_ID_53097891 m1A Human chr1 + 230426236 230426224 230426236 GGCTGCGGCCGAGACCAGGCGCCGCCGCCGCCACCGCCGCCACCACCGCCACCACCGCCGCCGCT GGCTGCGGCCGAGACCAGGCG____________CCGCCGCCACCACCGCCACCACCGCCGCCGCT GCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230426010..230426324 26863196 MeRIP-seq:(Medium) rs1342663446 Functional Loss DEL dbSNP153 22..33 33 - - - 86252 RMVar_ID_86252 Human_SNP_ID_53097899 m1A Human chr1 + 230426236 230426227 230426236 GGCTGCGGCCGAGACCAGGCGCCGCCGCCGCCACCGCCGCCACCACCGCCACCACCGCCGCCGCT GGCTGCGGCCGAGACCAGGCGCCG_________CCGCCGCCACCACCGCCACCACCGCCGCCGCT GCCGCCGCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230426010..230426324 26863196 MeRIP-seq:(Medium) rs1246975200 Functional Loss DEL dbSNP153 25..33 33 - - - 86253 RMVar_ID_86253 Human_SNP_ID_53097906 m1A Human chr1 + 230426236 230426236 230426236 GGCTGCGGCCGAGACCAGGCGCCGCCGCCGCCACCGCCGCCACCACCGCCACCACCGCCGCCGCT GGCTGCGGCCGAGACCAGGCGCCGCCGCCGCCGCCGCCGCCACCACCGCCACCACCGCCGCCGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230426010..230426324 26863196 MeRIP-seq:(Medium) rs1218086379 Functional Loss SNV dbSNP153 33..33 33 - - - 86254 RMVar_ID_86254 Human_SNP_ID_53097922 m1A Human chr1 - 230426268 230426259 230426268 GGGCAGGGAGGCGGCGGGCGCCGAGGAGACGCAGCGGCGGCGGTGGTGGCGGTGGTGGCGGCGGT GGGCAGGGAGGCGGCGGGCGCCGAGGAGACGC_________GGTGGTGGCGGTGGTGGCGGCGGT CGCCGCCGCT C PGBD5 Ensembl:ENSG00000177614 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230425673..230426353 26863196 MeRIP-seq:(Medium) rs1008474027 Functional Loss DEL dbSNP153 33..41 33 - - - 86255 RMVar_ID_86255 Human_SNP_ID_53156352 m1A Human chr1 + 230669926 230669926 230669926 TTAAGCAGTGACAACACTGCAGTGTACGAGGAAGGTGCAGGGAGTGCTGTGAGTGTGGAAAGGTG TTAAGCAGTGACAACACTGCAGTGTACGAGGACGGTGCAGGGAGTGCTGTGAGTGTGGAAAGGTG A C COG2 Ensembl:ENSG00000135775 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:230669820..230670062 26863196 MeRIP-seq:(Medium) rs1039377018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_802021,Human_RBP_ID_5776632,Human_RBP_ID_23372096 RMVar_hsa_circ_140375,RMVar_hsa_circ_88053,RMVar_hsa_circ_284997,RMVar_hsa_circ_311899,RMVar_hsa_circ_287220,RMVar_hsa_circ_69685,RMVar_hsa_circ_140378,RMVar_hsa_circ_140379,RMVar_hsa_circ_8200,RMVar_hsa_circ_140384,RMVar_hsa_circ_277717,RMVar_hsa_circ_279716,RMVar_hsa_circ_288981,RMVar_hsa_circ_140385,RMVar_hsa_circ_140383,RMVar_hsa_circ_140387,RMVar_hsa_circ_359931,RMVar_hsa_circ_367591,RMVar_hsa_circ_355041 86256 RMVar_ID_86256 Human_SNP_ID_53199301 m1A Human chr1 + 230837265 230837264 230837265 AAAGAAAGGGAGGCTCTTCCTGAAATCCACACAGGGGGGTGCGGCTCAGACGGGTGACAGACCCC AAAGAAAGGGAGGCTCTTCCTGAAATCCACAC_GGGGGGTGCGGCTCAGACGGGTGACAGACCCC CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:230837217..230837367 32194978 MeRIP-seq:(Medium) rs1160600538 Functional Loss DEL dbSNP153 33..33 33 - - - 86257 RMVar_ID_86257 Human_SNP_ID_53199303 m1A Human chr1 + 230837265 230837264 230837266 AAAGAAAGGGAGGCTCTTCCTGAAATCCACACAGGGGGGTGCGGCTCAGACGGGTGACAGACCCC AAAGAAAGGGAGGCTCTTCCTGAAATCCACAC__GGGGGTGCGGCTCAGACGGGTGACAGACCCC CAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:230837217..230837367 32194978 MeRIP-seq:(Medium) rs1491302698 Functional Loss DEL dbSNP153 33..34 33 - - - 86258 RMVar_ID_86258 Human_SNP_ID_53199706 m1A Human chr1 - 230839028 230839028 230839028 GACCTGTTGGTTGTTCCCCGGACTGGGCACCTACAGGAGTCAGGGCAGACGGCAGATGTGGCTGG GACCTGTTGGTTGTTCCCCGGACTGGGCACCTGCAGGAGTCAGGGCAGACGGCAGATGTGGCTGG T C C1orf198 Ensembl:ENSG00000119280 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1202549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_345524,Human_RBP_ID_5776805,Human_RBP_ID_8168722,Human_RBP_ID_10834611,Human_RBP_ID_22782761,Human_RBP_ID_26376795 Human_miRNA_ID_1398432,Human_miRNA_ID_2453267,Human_miRNA_ID_2454896,Human_miRNA_ID_3089697 RMVar_hsa_circ_90485,RMVar_hsa_circ_140390 86259 RMVar_ID_86259 Human_SNP_ID_53200940 m1A Human chr1 - 230843770 230843770 230843770 AGGGCTCCCAGGCCCTCAAGTCCTCCCAAGGCAGCAGGTCCTCCAGCCTGGACGCCCTGGGCCCC AGGGCTCCCAGGCCCTCAAGTCCTCCCAAGGCGGCAGGTCCTCCAGCCTGGACGCCCTGGGCCCC T C C1orf198 Ensembl:ENSG00000119280 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:230843722..230843828 26863196 MeRIP-seq:(Medium) rs778638875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_197884 Human_miRNA_ID_2510601,Human_miRNA_ID_2510602,Human_miRNA_ID_2510603,Human_miRNA_ID_3053423,Human_miRNA_ID_3053424,Human_miRNA_ID_3053425 RMVar_hsa_circ_88564,RMVar_hsa_circ_90485,RMVar_hsa_circ_288792,RMVar_hsa_circ_140390,RMVar_hsa_circ_363802,RMVar_hsa_circ_106015,RMVar_hsa_circ_140391,RMVar_hsa_circ_140392,RMVar_hsa_circ_140393 86260 RMVar_ID_86260 Human_SNP_ID_53206661 m1A Human chr1 - 230868392 230868392 230868392 TCACTTACTTCTCGTCGCTGAGCCCCATGGCCAGGAAGATCATGCAGGACAAGGAGAAGATCCGC TCACTTACTTCTCGTCGCTGAGCCCCATGGCCTGGAAGATCATGCAGGACAAGGAGAAGATCCGC T A C1orf198 Ensembl:ENSG00000119280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230868234..230868550 26863196 MeRIP-seq:(Medium) rs369977427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423674,Human_RBP_ID_4074841,Human_RBP_ID_5776855,Human_RBP_ID_10834759 Human_Splice_Rec_197874 Human_miRNA_ID_2254009,Human_miRNA_ID_2392244 RMVar_hsa_circ_88564,RMVar_hsa_circ_140393 86261 RMVar_ID_86261 Human_SNP_ID_53206662 m1A Human chr1 - 230868392 230868392 230868392 TCACTTACTTCTCGTCGCTGAGCCCCATGGCCAGGAAGATCATGCAGGACAAGGAGAAGATCCGC TCACTTACTTCTCGTCGCTGAGCCCCATGGCCGGGAAGATCATGCAGGACAAGGAGAAGATCCGC T C C1orf198 Ensembl:ENSG00000119280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230868234..230868550 26863196 MeRIP-seq:(Medium) rs369977427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423674,Human_RBP_ID_4074841,Human_RBP_ID_5776855,Human_RBP_ID_10834759 Human_Splice_Rec_197874 Human_miRNA_ID_2254009,Human_miRNA_ID_2392244 RMVar_hsa_circ_88564,RMVar_hsa_circ_140393 86262 RMVar_ID_86262 Human_SNP_ID_53206696 m1A Human chr1 + 230868476 230868474 230868476 GTCCAGAGGCCGGTTCCCGCTCATGACCGCCGAGCGCGAAGCCGCGATCGCCGCCGCCATGGACG GTCCAGAGGCCGGTTCCCGCTCATGACCGCC__GCGCGAAGCCGCGATCGCCGCCGCCATGGACG CGA C AL118511.1 Ensembl:ENSG00000223393 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr1:230868306..230868525;chr1:230868401..230868525 26863196,26863410 MeRIP-seq:(Medium) rs752874359 Functional Loss DEL dbSNP153 32..33 33 - - - 86263 RMVar_ID_86263 Human_SNP_ID_53232501 m1A Human chr1 + 230978815 230978815 230978815 AGCGCCGCCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCAGGTGCCATCTTCCCTCAAGGCGCAT AGCGCCGCCCCAGAAGCAGCAGCAGCAGCAGCGGCCGGCAGGTGCCATCTTCCCTCAAGGCGCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230978736..230978820 26863196 MeRIP-seq:(Medium) rs1003233326 Functional Loss SNV dbSNP153 33..33 33 - - - 86264 RMVar_ID_86264 Human_SNP_ID_53232502 m1A Human chr1 + 230978815 230978815 230978815 AGCGCCGCCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCAGGTGCCATCTTCCCTCAAGGCGCAT AGCGCCGCCCCAGAAGCAGCAGCAGCAGCAGCTGCCGGCAGGTGCCATCTTCCCTCAAGGCGCAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230978736..230978820 26863196 MeRIP-seq:(Medium) rs1003233326 Functional Loss SNV dbSNP153 33..33 33 - - - 86265 RMVar_ID_86265 Human_SNP_ID_53232510 m1A Human chr1 + 230978822 230978822 230978822 CCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCAGGTGCCATCTTCCCTCAAGGCGCATGCGCGAC CCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCCGGTGCCATCTTCCCTCAAGGCGCATGCGCGAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:230978159..230978834 26863196 MeRIP-seq:(Medium) rs1328612292 Functional Loss SNV dbSNP153 33..33 33 - - - 86266 RMVar_ID_86266 Human_SNP_ID_53232511 m1A Human chr1 + 230978822 230978822 230978822 CCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCAGGTGCCATCTTCCCTCAAGGCGCATGCGCGAC CCCCAGAAGCAGCAGCAGCAGCAGCAGCCGGCGGGTGCCATCTTCCCTCAAGGCGCATGCGCGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:230978159..230978834 26863196 MeRIP-seq:(Medium) rs1328612292 Functional Loss SNV dbSNP153 33..33 33 - - - 86267 RMVar_ID_86267 Human_SNP_ID_53232679 m1A Human chr1 - 230979152 230979152 230979152 AGGCAGCAGTAGGAGTCGCTGCCACCCCATCCACGTTCCCCTTCCCCTGCTGCAGGCCGCTCCGC AGGCAGCAGTAGGAGTCGCTGCCACCCCATCCCCGTTCCCCTTCCCCTGCTGCAGGCCGCTCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:230979101..230979250;chr1:230979101..230979275 26863196 MeRIP-seq:(Medium) rs1281545093 Functional Loss SNV dbSNP153 33..33 33 - - - 86268 RMVar_ID_86268 Human_SNP_ID_53232690 m1A Human chr1 + 230979175 230979175 230979175 AGGGGAACGTGGATGGGGTGGCAGCGACTCCTACTGCTGCCTCGGCCTCCTGCCAGTACAGGTGC AGGGGAACGTGGATGGGGTGGCAGCGACTCCTGCTGCTGCCTCGGCCTCCTGCCAGTACAGGTGC A G ARV1 Ensembl:ENSG00000173409 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:230979126..230979228 26863196 MeRIP-seq:(Medium) rs762304664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224574,Human_RBP_ID_1423688,Human_RBP_ID_4074842,Human_RBP_ID_5312894,Human_RBP_ID_5457216,Human_RBP_ID_5485675,Human_RBP_ID_8745149,Human_RBP_ID_9320409,Human_RBP_ID_17742630,Human_RBP_ID_18415152,Human_RBP_ID_22427870 Human_Splice_Rec_198101 86269 RMVar_ID_86269 Human_SNP_ID_53232714 m1A Human chr1 + 230979224 230979224 230979224 CTGCCAGTACAGGTGCATCGAATGCAACCAGGAGGCCAAAGAGTTGTACCGAGACTATAACCACG CTGCCAGTACAGGTGCATCGAATGCAACCAGGGGGCCAAAGAGTTGTACCGAGACTATAACCACG A G ARV1 Ensembl:ENSG00000173409 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230979115..230979250 26863196 MeRIP-seq:(Medium) rs368325339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423690,Human_RBP_ID_4074842,Human_RBP_ID_5312894,Human_RBP_ID_18415728,Human_RBP_ID_18566099 Human_Splice_Rec_198083,Human_Splice_Rec_198091,Human_Splice_Rec_198101,Human_Splice_Rec_198111,Human_Splice_Rec_198121 86270 RMVar_ID_86270 Human_SNP_ID_53237104 m1A Human chr1 + 230997129 230997129 230997129 TATTGGCTGCCTTCTCCTTTCCAGTGACCCTAAACATCAACCGTAAGCTCTCCTTCTTGGCCGTG TATTGGCTGCCTTCTCCTTTCCAGTGACCCTATACATCAACCGTAAGCTCTCCTTCTTGGCCGTG A T ARV1 Ensembl:ENSG00000173409 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1352432790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_198082,Human_Splice_Rec_198088,Human_Splice_Rec_198098,Human_Splice_Rec_198108,Human_Splice_Rec_198118,Human_Splice_Rec_198130,Human_Splice_Rec_198132 RMVar_hsa_circ_328564,RMVar_hsa_circ_140424,RMVar_hsa_circ_360468 86271 RMVar_ID_86271 Human_SNP_ID_53242759 m1A Human chr1 - 231019935 231019935 231019935 GAGCAGAACTCCCTGCACGACAGGAGGGACCGAGGCCCTCCTCGGGACTTGTCACTGCCTGTCTC GAGCAGAACTCCCTGCACGACAGGAGGGACCGGGGCCCTCCTCGGGACTTGTCACTGCCTGTCTC T C FAM89A Ensembl:ENSG00000182118 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs200478626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_345645,Human_RBP_ID_22024358 86272 RMVar_ID_86272 Human_SNP_ID_53247821 m1A Human chr1 - 231040211 231040166 231040211 GCGGGGCAGGCGCGTGGCCGGGCCGCGGCGCGATGAGTGGGGCCCGGGCGGCGCCCGGGGCCGCG GCGGGGCAGGCGCGTGGCCGGGCCGCGGCGCG_________________________________ CCGCGCCGTTGCCCGCGGCCCCGGGCGCCGCCCGGGCCCCACTCAT C FAM89A Ensembl:ENSG00000182118 Protein coding start codon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:231040111..231040237;chr1:231039952..231040233;chr1:231039974..231040249 26863196 MeRIP-seq:(Medium) rs1387441261 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_224638,Human_RBP_ID_4074843 86273 RMVar_ID_86273 Human_SNP_ID_53247826 m1A Human chr1 - 231040174 231040174 231040174 TGGGGCCCGGGCGGCGCCCGGGGCCGCGGGCAACGGCGCGGTCCGGGGGCTGCGGGTGGACGGGC TGGGGCCCGGGCGGCGCCCGGGGCCGCGGGCAGCGGCGCGGTCCGGGGGCTGCGGGTGGACGGGC T C FAM89A Ensembl:ENSG00000182118 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:231040076..231040275 26863410 MeRIP-seq:(Medium) rs1167104704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224638,Human_RBP_ID_4032098 86274 RMVar_ID_86274 Human_SNP_ID_53247834 m1A Human chr1 + 231040206 231040195 231040207 TTGCCCGCGGCCCCGGGCGCCGCCCGGGCCCCACTCATCGCGCCGCGGCCCGGCCACGCGCCTGC TTGCCCGCGGCCCCGGGCGCCG____________TCATCGCGCCGCGGCCCGGCCACGCGCCTGC GCCCGGGCCCCAC G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:231040115..231040239 26863410 MeRIP-seq:(Medium) rs1207646761 Functional Loss DEL dbSNP153 23..34 33 - - - 86275 RMVar_ID_86275 Human_SNP_ID_53247845 m1A Human chr1 + 231040206 231040204 231040206 TTGCCCGCGGCCCCGGGCGCCGCCCGGGCCCCACTCATCGCGCCGCGGCCCGGCCACGCGCCTGC TTGCCCGCGGCCCCGGGCGCCGCCCGGGCCC__CTCATCGCGCCGCGGCCCGGCCACGCGCCTGC CCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:231040115..231040239 26863410 MeRIP-seq:(Medium) rs1434642713 Functional Loss DEL dbSNP153 32..33 33 - - - 86276 RMVar_ID_86276 Human_SNP_ID_53299019 m1A Human chr1 + 231239007 231239007 231239007 ATCTCTGGTCCTGTGGGGGTCCCAGAAGGAGCACAATGCCGCTCTTCTCTAAGTTCCTTGAAGAA ATCTCTGGTCCTGTGGGGGTCCCAGAAGGAGCGCAATGCCGCTCTTCTCTAAGTTCCTTGAAGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:231238957..231239038 32194978 MeRIP-seq:(Medium) rs775767325 Functional Loss SNV dbSNP153 33..33 33 - - - 86277 RMVar_ID_86277 Human_SNP_ID_53299679 m1A Human chr1 + 231241306 231241306 231241306 CCTAGGCGAAGTAGGGCCGTCCTGAGCGAAAGAACCGCCCCCAGCAGGAGCACCACCACGGCTTA CCTAGGCGAAGTAGGGCCGTCCTGAGCGAAAGCACCGCCCCCAGCAGGAGCACCACCACGGCTTA A C GNPAT Ensembl:ENSG00000116906 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:231241256..231241414 26863196 MeRIP-seq:(Medium) rs1351084022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074845,Human_RBP_ID_18415153,Human_RBP_ID_26856566 86278 RMVar_ID_86278 Human_SNP_ID_53323541 m1A Human chr1 - 231337801 231337801 231337801 AGGAGCTCGGTTGGCCTTGGGTGGGTCTAGACAGCCGCGGCGGCTGCGGCGCCGATAGTGACAGT AGGAGCTCGGTTGGCCTTGGGTGGGTCTAGACGGCCGCGGCGGCTGCGGCGCCGATAGTGACAGT T C EXOC8 Ensembl:ENSG00000116903 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr1:231337634..231337850;chr1:231337676..231337850 26863196 MeRIP-seq:(Medium) rs536539431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744691,Human_RBP_ID_4074846,Human_RBP_ID_8940211 86279 RMVar_ID_86279 Human_SNP_ID_53330952 m1A Human chr1 + 231366079 231366075 231366080 AATTCAAACTTGATATAAAAAAGGGAGAGATGAAATGAACTCAGCTAGATAACAGATCTGGCAAA AATTCAAACTTGATATAAAAAAGGGAGAG_____ATGAACTCAGCTAGATAACAGATCTGGCAAA GATGAA G lnc-SPRTN-4,lnc-SPRTN-4:2,lnc-SPRTN-2 RNACentral:URS00009B08A5,RNACentral:URS00008B40E8,RNACentral:URS00008B2803 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:231365989..231366189 32194978 MeRIP-seq:(Medium) rs1440104165 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_10837415 86280 RMVar_ID_86280 Human_SNP_ID_53345240 m1A Human chr1 - 231421225 231421225 231421225 ACGACTTCCTCGGCAAGGAGACCGGACAGCAGATCGGCGACGAGGTGCGCGCCCTGCACGACACC ACGACTTCCTCGGCAAGGAGACCGGACAGCAGGTCGGCGACGAGGTGCGCGCCCTGCACGACACC T C EGLN1,AL445524.2 Ensembl:ENSG00000135766,Ensembl:ENSG00000287856 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:231421175..231421440 26863196 MeRIP-seq:(Medium) rs1201877205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_345934,Human_RBP_ID_744883,Human_RBP_ID_8964819,Human_RBP_ID_22026567 86281 RMVar_ID_86281 Human_SNP_ID_53345261 m1A Human chr1 - 231421270 231421270 231421270 AGTACATCGTGCCGTGCATGAACAAGCACGGCATCTGTGTGGTGGACGACTTCCTCGGCAAGGAG AGTACATCGTGCCGTGCATGAACAAGCACGGCGTCTGTGTGGTGGACGACTTCCTCGGCAAGGAG T C EGLN1,AL445524.2 Ensembl:ENSG00000135766,Ensembl:ENSG00000287856 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:231421222..231421362 26863196 MeRIP-seq:(Medium) rs760962608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_345935,Human_RBP_ID_1423876,Human_RBP_ID_5778128,Human_RBP_ID_8745312,Human_RBP_ID_17742944,Human_RBP_ID_22025696,Human_RBP_ID_27835443 86282 RMVar_ID_86282 Human_SNP_ID_53345451 m1A Human chr1 - 231421614 231421614 231421614 TGCAGTGCCGCCGCCCAGGGCCGGGGCCCGGGAGCCCAGGAAGGCAGCGGCGCGCCGGGACAACG TGCAGTGCCGCCGCCCAGGGCCGGGGCCCGGGCGCCCAGGAAGGCAGCGGCGCGCCGGGACAACG T G EGLN1,AL445524.2 Ensembl:ENSG00000135766,Ensembl:ENSG00000287856 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:231421526..231421910 26863410 MeRIP-seq:(Medium) rs553659934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855939,Human_RBP_ID_8754477,Human_RBP_ID_9270743 86283 RMVar_ID_86283 Human_SNP_ID_53345604 m1A Human chr1 + 231421908 231421899 231421908 TGTCATTGGCCATGGCGGCGGCGGCGGCGGCGACGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG TGTCATTGGCCATGGCGGCGGCGG_________CGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG GCGGCGGCGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:231421862..231421961 26863196 MeRIP-seq:(Medium) rs1443135648 Functional Loss DEL dbSNP153 25..33 33 - - - 86284 RMVar_ID_86284 Human_SNP_ID_53345613 m1A Human chr1 + 231421908 231421908 231421908 TGTCATTGGCCATGGCGGCGGCGGCGGCGGCGACGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG TGTCATTGGCCATGGCGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:231421862..231421961 26863196 MeRIP-seq:(Medium) rs756211725 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_458 86285 RMVar_ID_86285 Human_SNP_ID_53376565 m1A Human chr1 + 231557320 231557320 231557320 GAAGACATGACTAGAGAGGTGGAAAAGTGGGAAATCAGGAGATGATGCTGTCAAAGGAATCAAAG GAAGACATGACTAGAGAGGTGGAAAAGTGGGATATCAGGAGATGATGCTGTCAAAGGAATCAAAG A T TSNAX,TSNAX-DISC1 Ensembl:ENSG00000116918,Ensembl:ENSG00000270106 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:231557292..231557373 26863196 MeRIP-seq:(Medium) rs1339335918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15158,RMVar_hsa_circ_78988,RMVar_hsa_circ_104896,RMVar_hsa_circ_121400,RMVar_hsa_circ_140447,RMVar_hsa_circ_140448,RMVar_hsa_circ_140449 86286 RMVar_ID_86286 Human_SNP_ID_53434680 m1A Human chr1 - 231799967 231799967 231799967 GATGAAAAGTAATTGGAAGACAATGTTCAAAAAGCAAGCAATGGAAAAAGAAAGACAAAGAAGAG GATGAAAAGTAATTGGAAGACAATGTTCAAAATGCAAGCAATGGAAAAAGAAAGACAAAGAAGAG T A AL136171.2 Ensembl:ENSG00000286071 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:231799924..231800028 26863196 MeRIP-seq:(Medium) rs570158436 Functional Loss SNV dbSNP153 33..33 33 - - - 86287 RMVar_ID_86287 Human_SNP_ID_53442116 m1A Human chr1 - 231832085 231832085 231832085 ATTACCACTGTTCCTGGCATGGACTTCAATCCAGCCTCCCACATTATTCTGGATACCACACCTGA ATTACCACTGTTCCTGGCATGGACTTCAATCCGGCCTCCCACATTATTCTGGATACCACACCTGA T C AL136171.2 Ensembl:ENSG00000286071 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:231832076..231832166 26863196 MeRIP-seq:(Medium) rs76903597 Functional Loss SNV dbSNP153 33..33 33 - - - 86288 RMVar_ID_86288 Human_SNP_ID_53442529 m1A Human chr1 + 231833298 231833298 231833298 TAAGAGGTTTAGAAGCCTGGCCGTCAATATCTACAACAGTTATGGAGGCAAGGGAAACAGGCCCT TAAGAGGTTTAGAAGCCTGGCCGTCAATATCTGCAACAGTTATGGAGGCAAGGGAAACAGGCCCT A G DISC1 Ensembl:ENSG00000162946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:231833176..231833356 26863196 MeRIP-seq:(Medium) rs1260308362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67679,RMVar_hsa_circ_62566 86289 RMVar_ID_86289 Human_SNP_ID_53444936 m1A Human chr1 + 231843268 231843268 231843268 GAGAGGTGATAGAGAAAAGCTTCCTTATGGGGACCGCAAGAAGTTTAGTGGGGCTGCGTTGTTCA GAGAGGTGATAGAGAAAAGCTTCCTTATGGGGGCCGCAAGAAGTTTAGTGGGGCTGCGTTGTTCA A G DISC1 Ensembl:ENSG00000162946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:231843249..231843723 26863196 MeRIP-seq:(Medium) rs80336062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67679,RMVar_hsa_circ_62566 86290 RMVar_ID_86290 Human_SNP_ID_53454333 m1A Human chr1 + 231883438 231883438 231883438 GTGAAAGGAACAGTGCCAGCTGTTGCACAGGGACTTGTGATGAGGTTGGTGTGAGTGGGTGGCCA GTGAAAGGAACAGTGCCAGCTGTTGCACAGGGTCTTGTGATGAGGTTGGTGTGAGTGGGTGGCCA A T DISC1 Ensembl:ENSG00000162946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:231883410..231883493 26863196 MeRIP-seq:(Medium) rs567029228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67679,RMVar_hsa_circ_62566 86291 RMVar_ID_86291 Human_SNP_ID_53659930 m1A Human chr1 + 232725286 232725286 232725286 GAAAGGGAGGGGAGGGGAGGGGAGGGGAGGGGAGGGGGGGAGGGGAGGGGGGGAGGGGGGGAGGG GAAAGGGAGGGGAGGGGAGGGGAGGGGAGGGGGGGGGGGGAGGGGAGGGGGGGAGGGGGGGAGGG A G LINC01745,LINC01745:2,LINC01745:3,LINC01745:4,LINC01745:5,LINC01745:6,LINC01745:7 RNACentral:URS00008B58E9,RNACentral:URS00008B891E,RNACentral:URS00009B2DFA,RNACentral:URS00009BF0C1,RNACentral:URS00008B7DC3,RNACentral:URS00008BD8F3,RNACentral:URS00008BCB15 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:232725202..232725330 26863196 MeRIP-seq:(Medium) rs1203044952 Functional Loss SNV dbSNP153 33..33 33 - - - 86292 RMVar_ID_86292 Human_SNP_ID_53659959 m1A Human chr1 + 232725362 232725362 232725362 GGGGGAGGGGAGGGGAGGGGGGAGGGGAGGGGAGGGGGGGAGGGGGGGAGGGGGGGAGGGGAGGG GGGGGAGGGGAGGGGAGGGGGGAGGGGAGGGGGGGGGGGGAGGGGGGGAGGGGGGGAGGGGAGGG A G LINC01745,LINC01745:2,LINC01745:3,LINC01745:4,LINC01745:5,LINC01745:6,LINC01745:7 RNACentral:URS00008B58E9,RNACentral:URS00008B891E,RNACentral:URS00009B2DFA,RNACentral:URS00009BF0C1,RNACentral:URS00008B7DC3,RNACentral:URS00008BD8F3,RNACentral:URS00008BCB15 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:232725260..232725365 26863196 MeRIP-seq:(Medium) rs1376255523 Functional Loss SNV dbSNP153 33..33 33 - - - 86293 RMVar_ID_86293 Human_SNP_ID_53715477 m1A Human chr1 + 232950683 232950683 232950683 GAATTGCGACCCCAACCTGGACTGCTCCCCTGACCGCAACCCCTACCCCCGCCCACCAGTATGGC GAATTGCGACCCCAACCTGGACTGCTCCCCTGGCCGCAACCCCTACCCCCGCCCACCAGTATGGC A G NTPCR Ensembl:ENSG00000135778 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:232950635..232950789 26863196 MeRIP-seq:(Medium) rs758192601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346094,Human_RBP_ID_4074855 Human_Splice_Rec_199257,Human_Splice_Rec_199263,Human_Splice_Rec_199271,Human_Splice_Rec_199277,Human_Splice_Rec_199281 Human_miRNA_ID_3021110 RMVar_hsa_circ_140484,RMVar_hsa_circ_106216 86294 RMVar_ID_86294 Human_SNP_ID_53740510 m1A Human chr1 + 233059009 233059009 233059009 CTATCACTCCACCCTTTGCTTTCTTTGCTCCAAGCCTGTTGGTTTTCCTTTTCCACCCCTTCAGC CTATCACTCCACCCTTTGCTTTCTTTGCTCCACGCCTGTTGGTTTTCCTTTTCCACCCCTTCAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:233058959..233059140 26863196 MeRIP-seq:(Medium) rs1031327893 Functional Loss SNV dbSNP153 33..33 33 - - - 86295 RMVar_ID_86295 Human_SNP_ID_53740511 m1A Human chr1 + 233059009 233059009 233059009 CTATCACTCCACCCTTTGCTTTCTTTGCTCCAAGCCTGTTGGTTTTCCTTTTCCACCCCTTCAGC CTATCACTCCACCCTTTGCTTTCTTTGCTCCAGGCCTGTTGGTTTTCCTTTTCCACCCCTTCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:233058959..233059140 26863196 MeRIP-seq:(Medium) rs1031327893 Functional Loss SNV dbSNP153 33..33 33 - - - 86296 RMVar_ID_86296 Human_SNP_ID_53796191 m1A Human chr1 - 233295590 233295578 233295590 GGAAGGAGGCGGCGGGGGCGACGGCGGCGGCGACGGCGGGGGCGCGGCCCGCGGGCCCGGGTGTT GGAAGGAGGCGGCGGGGGCGACGGCGGCGGCG____________CGGCCCGCGGGCCCGGGTGTT GCGCCCCCGCCGT G PCNX2,AL133380.1 Ensembl:ENSG00000135749,Ensembl:ENSG00000251508 Protein coding,Pseudogene 5'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:233295501..233295674 26863196 MeRIP-seq:(Medium) rs1488525156 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_346196,Human_RBP_ID_5160475,Human_RBP_ID_8241525,Human_RBP_ID_21963728 Human_Splice_Rec_199579 86297 RMVar_ID_86297 Human_SNP_ID_53796192 m1A Human chr1 - 233295602 233295578 233295602 CAAACGTGGGGTGGAAGGAGGCGGCGGGGGCGACGGCGGCGGCGACGGCGGGGGCGCGGCCCGCG CAAACGTGGGGTGGAAGGAGGCGGCGGGGGCG________________________CGGCCCGCG GCGCCCCCGCCGTCGCCGCCGCCGT G PCNX2,AL133380.1 Ensembl:ENSG00000135749,Ensembl:ENSG00000251508 Protein coding,Pseudogene 5'UTR,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:233295526..233295648;chr1:233295375..233295710 26863196 MeRIP-seq:(Medium) rs976539371 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_5160475,Human_RBP_ID_18429768 Human_Splice_Rec_199579 86298 RMVar_ID_86298 Human_SNP_ID_53796201 m1A Human chr1 - 233295590 233295590 233295590 GGAAGGAGGCGGCGGGGGCGACGGCGGCGGCGACGGCGGGGGCGCGGCCCGCGGGCCCGGGTGTT GGAAGGAGGCGGCGGGGGCGACGGCGGCGGCGGCGGCGGGGGCGCGGCCCGCGGGCCCGGGTGTT T C PCNX2,AL133380.1 Ensembl:ENSG00000135749,Ensembl:ENSG00000251508 Protein coding,Pseudogene 5'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:233295501..233295674 26863196 MeRIP-seq:(Medium) rs1219619885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346196,Human_RBP_ID_5160475,Human_RBP_ID_8241525,Human_RBP_ID_21963728 Human_Splice_Rec_199579 86299 RMVar_ID_86299 Human_SNP_ID_53803840 m1A Human chr1 + 233328658 233328658 233328658 CTGGAGTTCGCCCGCGGCGGAGCGCTCAACCGAGCGCTGGCCGCTGCCAACGCCGCCCCGGACCC CTGGAGTTCGCCCGCGGCGGAGCGCTCAACCGCGCGCTGGCCGCTGCCAACGCCGCCCCGGACCC A C MAP3K21 Ensembl:ENSG00000143674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:233328617..233328737 26863196 MeRIP-seq:(Medium) rs1447408567 Functional Loss SNV dbSNP153 33..33 33 - - - 86300 RMVar_ID_86300 Human_SNP_ID_53887915 m1A Human chr1 + 233666700 233666700 233666700 CTTCACCCTCCTGTTCCTGACGGCTGTGGTCCAGCGCATCACCGTGCACGTCACCCGCAGGCCGG CTTCACCCTCCTGTTCCTGACGGCTGTGGTCCGGCGCATCACCGTGCACGTCACCCGCAGGCCGG A G KCNK1 Ensembl:ENSG00000135750 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:233666652..233666788 26863196 MeRIP-seq:(Medium) rs1225010491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346322 86301 RMVar_ID_86301 Human_SNP_ID_53893614 m1A Human chr1 + 233688041 233688041 233688041 TACGAGGTCGTGGCATGGAAATAAGGGATCAGAGCACAGAGATATAAGAGGTTGGGGCACGGAAA TACGAGGTCGTGGCATGGAAATAAGGGATCAGGGCACAGAGATATAAGAGGTTGGGGCACGGAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:233687991..233688189 26863196 MeRIP-seq:(Medium) rs538286945 Functional Loss SNV dbSNP153 33..33 33 - - - 86302 RMVar_ID_86302 Human_SNP_ID_53893642 m1A Human chr1 - 233688110 233688110 233688110 TATATCTCTGTGCCCTGATCCTTTATTTCCGCACCCCGACCTCTTATATCTCTGTGCCCCGATCC TATATCTCTGTGCCCTGATCCTTTATTTCCGCGCCCCGACCTCTTATATCTCTGTGCCCCGATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:233687988..233688200 26863196 MeRIP-seq:(Medium) rs1440352474 Functional Loss SNV dbSNP153 33..33 33 - - - 86303 RMVar_ID_86303 Human_SNP_ID_53990375 m1A Human chr1 - 234097971 234097971 234097971 ACACCGTCACTACCACCACCATCTGAACTGCCACCACCAACACAGTCACCACCTCCACCATCACC ACACCGTCACTACCACCACCATCTGAACTGCCGCCACCAACACAGTCACCACCTCCACCATCACC T C lnc-TARBP1-7 RNACentral:URS00008B5E52 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:234097957..234098306 26863196 MeRIP-seq:(Medium) rs1303105291 Functional Loss SNV dbSNP153 33..33 33 - - - 86304 RMVar_ID_86304 Human_SNP_ID_53990414 m1A Human chr1 + 234098069 234098066 234098069 GTGGTGGTGGTGGCAGTTCAGATGGTGGTGGTAGTGATGGTGTCATAGGGTGATGATGGAGGTGG GTGGTGGTGGTGGCAGTTCAGATGGTGGTG___GTGATGGTGTCATAGGGTGATGATGGAGGTGG GGTA G SLC35F3 Ensembl:ENSG00000183780 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:234097970..234098174 26863196 MeRIP-seq:(Medium) rs1000142780 Functional Loss DEL dbSNP153 31..33 33 - - - 86305 RMVar_ID_86305 Human_SNP_ID_53990722 m1A Human chr1 - 234098805 234098805 234098805 AGTCACCACCTCCATCATGACCCTATAACACCATCACTACCACCGCCATCTGAACTGCCACCACC AGTCACCACCTCCATCATGACCCTATAACACCGTCACTACCACCGCCATCTGAACTGCCACCACC T C lnc-TARBP1-7 RNACentral:URS00008B5E52 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234098424..234099090 26863196 MeRIP-seq:(Medium) rs568662992 Functional Loss SNV dbSNP153 33..33 33 - - - 86306 RMVar_ID_86306 Human_SNP_ID_53998112 m1A Human chr1 + 234128417 234128417 234128417 TGAGGCTGACCAGGGGTGAAGCAGGGCTGAAGAGTCTCTGGGTTAGAAGGTGCTGGCCAGTTGCA TGAGGCTGACCAGGGGTGAAGCAGGGCTGAAGGGTCTCTGGGTTAGAAGGTGCTGGCCAGTTGCA A G SLC35F3 Ensembl:ENSG00000183780 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234128412..234128613 26863196 MeRIP-seq:(Medium) rs1282092719 Functional Loss SNV dbSNP153 33..33 33 - - - 86307 RMVar_ID_86307 Human_SNP_ID_54000147 m1A Human chr1 + 234137312 234137312 234137312 GAGGTGGCAGAAAAACCAGGTGGCAGGAGGGCAATTCAGAGATCAACAGTGGGCAAGCCTGAGAG GAGGTGGCAGAAAAACCAGGTGGCAGGAGGGCGATTCAGAGATCAACAGTGGGCAAGCCTGAGAG A G SLC35F3 Ensembl:ENSG00000183780 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:234137288..234137386;chr1:234137280..234137401 26863196 MeRIP-seq:(Medium) rs944840313 Functional Loss SNV dbSNP153 33..33 33 - - - 86308 RMVar_ID_86308 Human_SNP_ID_54000259 m1A Human chr1 + 234137778 234137777 234137778 GCACATGTCGCAGCAAGTAGCTGCAAATTAGCAGGAGAGACAGGGTCTCCACTGAAGACAGCAGC GCACATGTCGCAGCAAGTAGCTGCAAATTAGC_GGAGAGACAGGGTCTCCACTGAAGACAGCAGC CA C SLC35F3 Ensembl:ENSG00000183780 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234137774..234137874 26863196 MeRIP-seq:(Medium) rs1181463170 Functional Loss DEL dbSNP153 33..33 33 - - - 86309 RMVar_ID_86309 Human_SNP_ID_54053211 m1A Human chr1 - 234356978 234356978 234356978 GCTGAACCGGGGCCTGCGGCGGAAGCGGCACTACCTGCTGAAGCGCCTGCGCAAGGCCAAGAAGG GCTGAACCGGGGCCTGCGGCGGAAGCGGCACTCCCTGCTGAAGCGCCTGCGCAAGGCCAAGAAGG T G AL355472.1 Ensembl:ENSG00000235605 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879245217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1836648,Human_miRNA_ID_1836791,Human_miRNA_ID_1841302,Human_miRNA_ID_1862794,Human_miRNA_ID_1865494,Human_miRNA_ID_1908529 86310 RMVar_ID_86310 Human_SNP_ID_54057647 m1A Human chr1 + 234373677 234373677 234373677 ATCGAAAGGAAGCCGGACGTGGGCGGGCAGAGAGGTCGGCTTGCTGATGGGTCCGGGTGGGGCGC ATCGAAAGGAAGCCGGACGTGGGCGGGCAGAGGGGTCGGCTTGCTGATGGGTCCGGGTGGGGCGC A G COA6 Ensembl:ENSG00000168275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:234373449..234373726 26863196 MeRIP-seq:(Medium) rs760224357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855946,Human_RBP_ID_4077215 Human_Splice_Rec_199697,Human_Splice_Rec_199701 86311 RMVar_ID_86311 Human_SNP_ID_54057883 m1A Human chr1 + 234374251 234374251 234374251 TTGGCCAACAGCTTCATCGCAGTAGGAATGGCAGCCCCATCTATGAAGGAAAGACAGGTCTGCTG TTGGCCAACAGCTTCATCGCAGTAGGAATGGCGGCCCCATCTATGAAGGAAAGACAGGTCTGCTG A G COA6 Ensembl:ENSG00000168275 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234374226..234374330 26863196 MeRIP-seq:(Medium) rs766294438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22896,Human_RBP_ID_346417,Human_RBP_ID_1424378,Human_RBP_ID_4033753,Human_RBP_ID_8940055,Human_RBP_ID_23374404 Human_Splice_Rec_199698,Human_Splice_Rec_199702,Human_Splice_Rec_199706 Human_miRNA_ID_2194354,Human_miRNA_ID_2533784,Human_miRNA_ID_2535515 RMVar_hsa_circ_99846,RMVar_hsa_circ_140609 86312 RMVar_ID_86312 Human_SNP_ID_54065597 m1A Human chr1 + 234401910 234401910 234401910 GACAGGAGTGAGAGATCTTTCTTCTTCCTGCCACCTCCTTACCCACCTGTCCTCTTTTCTCCTTC GACAGGAGTGAGAGATCTTTCTTCTTCCTGCCGCCTCCTTACCCACCTGTCCTCTTTTCTCCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234401832..234401996 26863196 MeRIP-seq:(Medium) rs1030394293 Functional Loss SNV dbSNP153 33..33 33 - - - 86313 RMVar_ID_86313 Human_SNP_ID_54067299 m1A Human chr1 - 234408669 234408669 234408669 AATCATAAGGAATTGAGGTGTCCTTTTGTGCTAAGTCAGTTCCAGGGTGGGGGCCACGAGATCAG AATCATAAGGAATTGAGGTGTCCTTTTGTGCTGAGTCAGTTCCAGGGTGGGGGCCACGAGATCAG T C TARBP1 Ensembl:ENSG00000059588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:234408621..234408719 26863196 MeRIP-seq:(Medium) rs1242964928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8965205,Human_RBP_ID_10845701,Human_RBP_ID_18566981 RMVar_hsa_circ_10282,RMVar_hsa_circ_78447,RMVar_hsa_circ_83641,RMVar_hsa_circ_54777,RMVar_hsa_circ_140610,RMVar_hsa_circ_88691,RMVar_hsa_circ_115186,RMVar_hsa_circ_7872,RMVar_hsa_circ_140612,RMVar_hsa_circ_140613,RMVar_hsa_circ_78981,RMVar_hsa_circ_13205,RMVar_hsa_circ_140614,RMVar_hsa_circ_140616,RMVar_hsa_circ_355872,RMVar_hsa_circ_360091,RMVar_hsa_circ_363557,RMVar_hsa_circ_89482,RMVar_hsa_circ_113067,RMVar_hsa_circ_140617,RMVar_hsa_circ_335038,RMVar_hsa_circ_140618 86314 RMVar_ID_86314 Human_SNP_ID_54067307 m1A Human chr1 - 234408691 234408691 234408691 TGATTGGTTGGGTCGGAGATGAAATCATAAGGAATTGAGGTGTCCTTTTGTGCTAAGTCAGTTCC TGATTGGTTGGGTCGGAGATGAAATCATAAGGCATTGAGGTGTCCTTTTGTGCTAAGTCAGTTCC T G TARBP1 Ensembl:ENSG00000059588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:234408641..234408713 26863196 MeRIP-seq:(Medium) rs1161391718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9412212,Human_RBP_ID_10845702,Human_RBP_ID_23374455 RMVar_hsa_circ_10282,RMVar_hsa_circ_78447,RMVar_hsa_circ_83641,RMVar_hsa_circ_54777,RMVar_hsa_circ_140610,RMVar_hsa_circ_88691,RMVar_hsa_circ_115186,RMVar_hsa_circ_7872,RMVar_hsa_circ_140612,RMVar_hsa_circ_140613,RMVar_hsa_circ_78981,RMVar_hsa_circ_13205,RMVar_hsa_circ_140614,RMVar_hsa_circ_140616,RMVar_hsa_circ_355872,RMVar_hsa_circ_360091,RMVar_hsa_circ_363557,RMVar_hsa_circ_89482,RMVar_hsa_circ_113067,RMVar_hsa_circ_140617,RMVar_hsa_circ_335038,RMVar_hsa_circ_140618 86315 RMVar_ID_86315 Human_SNP_ID_54084899 m1A Human chr1 - 234478202 234478202 234478202 GGCGGTGGAGGTGTCGGCGGAGCTGGGGGCCGACTGCACCTGCGGGCCCCAGGAAGGAAACGGTA GGCGGTGGAGGTGTCGGCGGAGCTGGGGGCCGGCTGCACCTGCGGGCCCCAGGAAGGAAACGGTA T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:234472792..234478355 32194978 MeRIP-seq:(Medium) rs770335464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223534,Human_RBP_ID_5519400 Human_Splice_Rec_199711 86316 RMVar_ID_86316 Human_SNP_ID_54084959 m1A Human chr1 - 234478280 234478280 234478280 CTTCTGGAGGACGGTGCAGGCGGGGCTGGGCCAGGCGGACGCCCTGACGCGCAAGCGAGCGCGCT CTTCTGGAGGACGGTGCAGGCGGGGCTGGGCCGGGCGGACGCCCTGACGCGCAAGCGAGCGCGCT T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:234478226..234478400 26863196 MeRIP-seq:(Medium) rs761905583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879,Human_RBP_ID_223534,Human_RBP_ID_746167,Human_RBP_ID_3330589,Human_RBP_ID_5520015,Human_RBP_ID_8724706,Human_RBP_ID_17668331,Human_RBP_ID_18474425 86317 RMVar_ID_86317 Human_SNP_ID_54085051 m1A Human chr1 - 234478421 234478419 234478422 TGGGGCGTCCCTGGGGTCCGGCCGCGTAGAGGAGAAGCTGCTGGTCCTGAGCGCCCTGGCCGAGA TGGGGCGTCCCTGGGGTCCGGCCGCGTAGAG___AAGCTGCTGGTCCTGAGCGCCCTGGCCGAGA TCTC T TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:234478151..234478750;chr1:234478151..234479150 26863196 MeRIP-seq:(Medium) rs1271668374 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3328919,Human_RBP_ID_4033922,Human_RBP_ID_8724960,Human_RBP_ID_9412708,Human_RBP_ID_17101342,Human_RBP_ID_18415890,Human_RBP_ID_22707223 86318 RMVar_ID_86318 Human_SNP_ID_54085096 m1A Human chr1 - 234478501 234478501 234478501 GTGGCCGGGCGACTGCTGCCAGTGCTGGTCCAATGTGGCGGGGCGGCGCTGCGGGCCGTGTGGGG GTGGCCGGGCGACTGCTGCCAGTGCTGGTCCAGTGTGGCGGGGCGGCGCTGCGGGCCGTGTGGGG T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:234478453..234478703 26863196 MeRIP-seq:(Medium) rs1441129631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17099951,Human_RBP_ID_17743603,Human_RBP_ID_18474426 86319 RMVar_ID_86319 Human_SNP_ID_54085131 m1A Human chr1 - 234478574 234478574 234478574 CGCCGTCGCCCTGGCGCTGGGCGGGGGCGGGGACGGGGATGAGGCCGGGCCTGCCGAGGACGCGG CGCCGTCGCCCTGGCGCTGGGCGGGGGCGGGGGCGGGGATGAGGCCGGGCCTGCCGAGGACGCGG T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr1:234478275..234478625;chr1:234478151..234479140 26863196 MeRIP-seq:(Medium) rs1469394116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223537,Human_RBP_ID_801745,Human_RBP_ID_3328920,Human_RBP_ID_5312023,Human_RBP_ID_8724708,Human_RBP_ID_8754482,Human_RBP_ID_9319464,Human_RBP_ID_9410742,Human_RBP_ID_17099952,Human_RBP_ID_18455759,Human_RBP_ID_18474426,Human_RBP_ID_22026568 86320 RMVar_ID_86320 Human_SNP_ID_54085189 m1A Human chr1 - 234478657 234478657 234478657 GCTGCCGTGGAAGTGCTAGCAGCCGTCGGGCCATGTTTGCGGCCCCGCGAGGACGGGCCGCTACT GCTGCCGTGGAAGTGCTAGCAGCCGTCGGGCCCTGTTTGCGGCCCCGCGAGGACGGGCCGCTACT T G TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:234478498..234478703 26863196 MeRIP-seq:(Medium) rs1183889056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10846364,Human_RBP_ID_17099953,Human_RBP_ID_22026568 86321 RMVar_ID_86321 Human_SNP_ID_54085294 m1A Human chr1 + 234478909 234478909 234478909 AGGCTCCGCAGCAGTGGCACGAGGTACCCTGCAGCCACCTCGCGCGCCGCCTCCGGGAGCGCGCC AGGCTCCGCAGCAGTGGCACGAGGTACCCTGCGGCCACCTCGCGCGCCGCCTCCGGGAGCGCGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:234478906..234479130 26863196 MeRIP-seq:(Medium) rs1476880265 Functional Loss SNV dbSNP153 33..33 33 - - - 86322 RMVar_ID_86322 Human_SNP_ID_54118244 m1A Human chr1 - 234607372 234607372 234607372 AACCAGTGCCCCGCTGTGCTGCACCCTCTGCCACGAGCGGCTGGAGGACACCCATTTTGTGCAGT AACCAGTGCCCCGCTGTGCTGCACCCTCTGCCGCGAGCGGCTGGAGGACACCCATTTTGTGCAGT T C IRF2BP2 Ensembl:ENSG00000168264 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:234607326..234607375 26863196 MeRIP-seq:(Medium) rs760768510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4034057,Human_RBP_ID_8745744,Human_RBP_ID_9268201,Human_RBP_ID_10846583,Human_RBP_ID_17338706,Human_RBP_ID_17677044,Human_RBP_ID_17743663,Human_RBP_ID_22024385,Human_RBP_ID_22427875,Human_RBP_ID_26857306,Human_RBP_ID_27178379,Human_RBP_ID_27395574 86323 RMVar_ID_86323 Human_SNP_ID_54118435 m1A Human chr1 - 234607783 234607783 234607783 ACCAGAAGGTGAAGTCGGGCCCCCTAAGATCAACGGAGAGGCCCAGCCGTGGCTGTCCACATCCA ACCAGAAGGTGAAGTCGGGCCCCCTAAGATCATCGGAGAGGCCCAGCCGTGGCTGTCCACATCCA T A IRF2BP2 Ensembl:ENSG00000168264 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:234607599..234607799 32194978 MeRIP-seq:(Medium) rs765235768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745538,Human_RBP_ID_853303,Human_RBP_ID_1424448,Human_RBP_ID_4034074,Human_RBP_ID_5155977,Human_RBP_ID_9253192,Human_RBP_ID_10846605,Human_RBP_ID_17222123,Human_RBP_ID_17338712,Human_RBP_ID_18187892,Human_RBP_ID_26857315,Human_RBP_ID_27178384,Human_RBP_ID_27395594,Human_RBP_ID_27555086 Human_Splice_Rec_199856,Human_Splice_Rec_199858 86324 RMVar_ID_86324 Human_SNP_ID_54118459 m1A Human chr1 - 234607832 234607832 234607832 TTGTGTTTCCAGTTGCAAGAACAGCAAGGAAAAGGAAGCCCTCTCCAGAACCAGAAGGTGAAGTC TTGTGTTTCCAGTTGCAAGAACAGCAAGGAAACGGAAGCCCTCTCCAGAACCAGAAGGTGAAGTC T G IRF2BP2 Ensembl:ENSG00000168264 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:234607531..234607852 26863196 MeRIP-seq:(Medium) rs1171662395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853303,Human_RBP_ID_1424448,Human_RBP_ID_1740711,Human_RBP_ID_4034081,Human_RBP_ID_8302989,Human_RBP_ID_9253192,Human_RBP_ID_18187892,Human_RBP_ID_22025709,Human_RBP_ID_26312888 Human_Splice_Rec_199856,Human_Splice_Rec_199858 86325 RMVar_ID_86325 Human_SNP_ID_54118853 m1A Human chr1 - 234608557 234608557 234608557 CAAGACCGTGCGCGACACGCTGCTGGCGCTGCACCAGCACGGCCACTCGGGGCCCTTCGAGAGCA CAAGACCGTGCGCGACACGCTGCTGGCGCTGCCCCAGCACGGCCACTCGGGGCCCTTCGAGAGCA T G IRF2BP2 Ensembl:ENSG00000168264 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:234608506..234609072 26863196 MeRIP-seq:(Medium) rs1189622050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8755442,Human_RBP_ID_17743669 86326 RMVar_ID_86326 Human_SNP_ID_54119829 m1A Human chr1 + 234609964 234609964 234609964 GGGGGCAGGGGGCGGGGGGCGGCCGCCGGGGCAGGCTCAGCCCGAGCGGCGGGGCATGCCGCGCC GGGGGCAGGGGGCGGGGGGCGGCCGCCGGGGCTGGCTCAGCCCGAGCGGCGGGGCATGCCGCGCC A T HSALNG0011617 RNACentral:URS0000EA1E7E lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Starvation treatment chr1:234609701..234610156;chr1:234609725..234610128 26863196,26863410 MeRIP-seq:(Medium) rs1390125080 Functional Loss SNV dbSNP153 33..33 33 - - - 86327 RMVar_ID_86327 Human_SNP_ID_54119842 m1A Human chr1 - 234610001 234610001 234610001 GCGCCCGAGCTCCACGCCGCCCGGCCGCCGCCACCCCGGCGCGGCATGCCCCGCCGCTCGGGCTG GCGCCCGAGCTCCACGCCGCCCGGCCGCCGCCCCCCCGGCGCGGCATGCCCCGCCGCTCGGGCTG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr1:234609401..234610175;chr1:234609736..234610126 26863410 MeRIP-seq:(Medium) rs911639353 Functional Loss SNV dbSNP153 33..33 33 - - - 86328 RMVar_ID_86328 Human_SNP_ID_54119858 m1A Human chr1 - 234610049 234610049 234610049 GACGCCAGGAGCTGTGAGAGAGCGGCGGAGCGACCCGGGGCCCGCGCCGCGCCCGAGCTCCACGC GACGCCAGGAGCTGTGAGAGAGCGGCGGAGCGGCCCGGGGCCCGCGCCGCGCCCGAGCTCCACGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr1:234608821..234610200;chr1:234609839..234610175 26863196,26863410 MeRIP-seq:(Medium) rs1198422212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4034152 86329 RMVar_ID_86329 Human_SNP_ID_54244312 m1A Human chr1 - 235110799 235110799 235110799 TGTTGAACTGAGGAGCATTTCTCATTGTAAAGATTGCCTTTGTTCTGTCTAAAAGTCTGGAGAAA TGTTGAACTGAGGAGCATTTCTCATTGTAAAGGTTGCCTTTGTTCTGTCTAAAAGTCTGGAGAAA T C TOMM20 Ensembl:ENSG00000173726 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs752663031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346621,Human_RBP_ID_1424728,Human_RBP_ID_1740781,Human_RBP_ID_3303319,Human_RBP_ID_10848498,Human_RBP_ID_23374817 Human_miRNA_ID_1757644 RMVar_hsa_circ_97201,RMVar_hsa_circ_118777,RMVar_hsa_circ_126493,RMVar_hsa_circ_116089,RMVar_hsa_circ_140668,RMVar_hsa_circ_140669,RMVar_hsa_circ_140670,RMVar_hsa_circ_140667 86330 RMVar_ID_86330 Human_SNP_ID_54249253 m1A Human chr1 + 235128723 235128723 235128723 CGATGGCGCTGTTCCGACCCACCATCTTCTCTACAACGCTGAGCGTGGACGGTGGCGGCAGGGAC CGATGGCGCTGTTCCGACCCACCATCTTCTCTGCAACGCTGAGCGTGGACGGTGGCGGCAGGGAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:235128673..235128850 26863196 MeRIP-seq:(Medium) rs201689707 Functional Loss SNV dbSNP153 33..33 33 - - - 86331 RMVar_ID_86331 Human_SNP_ID_54249292 m1A Human chr1 + 235128779 235128779 235128779 GGCAGGGACCGCGAAGGAGCGGTGGGCCACGAACCCTCAGAGCGGTCGGCGCAGCTCACACCCGA GGCAGGGACCGCGAAGGAGCGGTGGGCCACGAGCCCTCAGAGCGGTCGGCGCAGCTCACACCCGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:235128576..235128825 26863196 MeRIP-seq:(Medium) rs1368622186 Functional Loss SNV dbSNP153 33..33 33 - - - 86332 RMVar_ID_86332 Human_SNP_ID_54249324 m1A Human chr1 + 235128824 235128824 235128824 TCGGCGCAGCTCACACCCGACGGCCGCGGGCCAGGAACACAGAAAGGCCGAGCACACGCCACTTC TCGGCGCAGCTCACACCCGACGGCCGCGGGCCGGGAACACAGAAAGGCCGAGCACACGCCACTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:235128776..235128825 32194978 MeRIP-seq:(Medium) rs1425895441 Functional Loss SNV dbSNP153 33..33 33 - - - 86333 RMVar_ID_86333 Human_SNP_ID_54251477 m1A Human chr1 - 235136069 235136069 235136069 ATTTTTATTAACTGTCTTTTTGTTTCAGAGAGACAAGAGATCGGTTTTTGTGGGGAATCTCCCTT ATTTTTATTAACTGTCTTTTTGTTTCAGAGAGTCAAGAGATCGGTTTTTGTGGGGAATCTCCCTT T A ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:235136035..235138096 32194978 MeRIP-seq:(Medium) rs778841894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855955,Human_RBP_ID_10849406,Human_RBP_ID_22639031 Human_Splice_Rec_200024,Human_Splice_Rec_200025,Human_Splice_Rec_200029,Human_Splice_Rec_200046,Human_Splice_Rec_200047,Human_Splice_Rec_200064,Human_Splice_Rec_200065,Human_Splice_Rec_200126,Human_Splice_Rec_200127 RMVar_hsa_circ_111668,RMVar_hsa_circ_140674,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_341333,RMVar_hsa_circ_304133,RMVar_hsa_circ_45021,RMVar_hsa_circ_140675,RMVar_hsa_circ_140673 86334 RMVar_ID_86334 Human_SNP_ID_54258539 m1A Human chr1 + 235160943 235160943 235160943 CACGGGTTGAATCTGGGGCTCCAGAGAACTGAAGAGGGACGCCAGCCGACCGGTGCCACCTCTGG CACGGGTTGAATCTGGGGCTCCAGAGAACTGACGAGGGACGCCAGCCGACCGGTGCCACCTCTGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:235160876..235160975 32194978 MeRIP-seq:(Medium) rs1467321662 Functional Loss SNV dbSNP153 33..33 33 - - - 86335 RMVar_ID_86335 Human_SNP_ID_54258540 m1A Human chr1 + 235160943 235160943 235160943 CACGGGTTGAATCTGGGGCTCCAGAGAACTGAAGAGGGACGCCAGCCGACCGGTGCCACCTCTGG CACGGGTTGAATCTGGGGCTCCAGAGAACTGAGGAGGGACGCCAGCCGACCGGTGCCACCTCTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:235160876..235160975 32194978 MeRIP-seq:(Medium) rs1467321662 Functional Loss SNV dbSNP153 33..33 33 - - - 86336 RMVar_ID_86336 Human_SNP_ID_54258566 m1A Human chr1 - 235161011 235161004 235161011 CGGGAGTCCGCCGGAAGACTACAGGCTTGGACAGGTCGCCAGTAGCTTATTTCGCGGCGAACACC CGGGAGTCCGCCGGAAGACTACAGGCTTGGAC_______CAGTAGCTTATTTCGCGGCGAACACC GGCGACCT G ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:235160876..235161109 32194978 MeRIP-seq:(Medium) rs1403037785 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_800994,Human_RBP_ID_4034386,Human_RBP_ID_10850119,Human_RBP_ID_17743845,Human_RBP_ID_18969735,Human_RBP_ID_22427879,Human_RBP_ID_22871080,Human_RBP_ID_26312893,Human_RBP_ID_26857425,Human_RBP_ID_27799370 Human_Splice_Rec_200010,Human_Splice_Rec_200034,Human_Splice_Rec_200052,Human_Splice_Rec_200068,Human_Splice_Rec_200080,Human_Splice_Rec_200090,Human_Splice_Rec_200094,Human_Splice_Rec_200112 RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_63868,RMVar_hsa_circ_339173 86337 RMVar_ID_86337 Human_SNP_ID_54272889 m1A Human chr1 - 235213999 235213993 235213999 TCAAGAGATGAAACGAATAAAGAAGAAGATGAAGATGATGAAGAAGCAGAAGAGGAGGAGGAGGA TCAAGAGATGAAACGAATAAAGAAGAAGATGA______TGAAGAAGCAGAAGAGGAGGAGGAGGA ATCATCT A ARID4B Ensembl:ENSG00000054267 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:235213831..235214064 26863196 MeRIP-seq:(Medium) rs1358835244 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_17049,Human_RBP_ID_190708,Human_RBP_ID_855961,Human_RBP_ID_1438254,Human_RBP_ID_2182527,Human_RBP_ID_5783478,Human_RBP_ID_8240603,Human_RBP_ID_17451097,Human_RBP_ID_22487414,Human_RBP_ID_22871083,Human_RBP_ID_23117584,Human_RBP_ID_24541385,Human_RBP_ID_26312906,Human_RBP_ID_27801675 Human_Splice_Rec_200162,Human_Splice_Rec_200252,Human_Splice_Rec_200298,Human_Splice_Rec_200382 RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_70320,RMVar_hsa_circ_59025,RMVar_hsa_circ_109816,RMVar_hsa_circ_347314,RMVar_hsa_circ_59555,RMVar_hsa_circ_20448,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_369816,RMVar_hsa_circ_37336,RMVar_hsa_circ_140688,RMVar_hsa_circ_140687,RMVar_hsa_circ_58307,RMVar_hsa_circ_140686,RMVar_hsa_circ_354232,RMVar_hsa_circ_364215,RMVar_hsa_circ_298639,RMVar_hsa_circ_58971,RMVar_hsa_circ_352368,RMVar_hsa_circ_74498,RMVar_hsa_circ_140689,RMVar_hsa_circ_355731,RMVar_hsa_circ_352984,RMVar_hsa_circ_368977,RMVar_hsa_circ_304182,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_140690,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692 86338 RMVar_ID_86338 Human_SNP_ID_54272892 m1A Human chr1 - 235213999 235213999 235213999 TCAAGAGATGAAACGAATAAAGAAGAAGATGAAGATGATGAAGAAGCAGAAGAGGAGGAGGAGGA TCAAGAGATGAAACGAATAAAGAAGAAGATGATGATGATGAAGAAGCAGAAGAGGAGGAGGAGGA T A ARID4B Ensembl:ENSG00000054267 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:235213831..235214064 26863196 MeRIP-seq:(Medium) rs1159818656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17049,Human_RBP_ID_190708,Human_RBP_ID_855961,Human_RBP_ID_1438254,Human_RBP_ID_2182527,Human_RBP_ID_5783478,Human_RBP_ID_8240603,Human_RBP_ID_17451097,Human_RBP_ID_22487414,Human_RBP_ID_22871083,Human_RBP_ID_23117584,Human_RBP_ID_24541385,Human_RBP_ID_26312906,Human_RBP_ID_27801675 Human_Splice_Rec_200162,Human_Splice_Rec_200252,Human_Splice_Rec_200298,Human_Splice_Rec_200382 RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_70320,RMVar_hsa_circ_59025,RMVar_hsa_circ_109816,RMVar_hsa_circ_347314,RMVar_hsa_circ_59555,RMVar_hsa_circ_20448,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_369816,RMVar_hsa_circ_37336,RMVar_hsa_circ_140688,RMVar_hsa_circ_140687,RMVar_hsa_circ_58307,RMVar_hsa_circ_140686,RMVar_hsa_circ_354232,RMVar_hsa_circ_364215,RMVar_hsa_circ_298639,RMVar_hsa_circ_58971,RMVar_hsa_circ_352368,RMVar_hsa_circ_74498,RMVar_hsa_circ_140689,RMVar_hsa_circ_355731,RMVar_hsa_circ_352984,RMVar_hsa_circ_368977,RMVar_hsa_circ_304182,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_140690,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692 86339 RMVar_ID_86339 Human_SNP_ID_54274485 m1A Human chr1 + 235219755 235219755 235219755 CACATACAAAGAGCAAATGATAAGAATCCATCAAGCTGAAATGCATCGTAACCAAAAACAATTTT CACATACAAAGAGCAAATGATAAGAATCCATCCAGCTGAAATGCATCGTAACCAAAAACAATTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:235219752..235219877 26863196 MeRIP-seq:(Medium) rs1378925429 Functional Loss SNV dbSNP153 33..33 33 - - - 86340 RMVar_ID_86340 Human_SNP_ID_54303758 m1A Human chr1 + 235328628 235328626 235328629 TGCACCAACTAATGCGGTGTCGCTGGCGGCTGAGGAGGGCGGAGAGTTCTGTGGTGAAATAGTGG TGCACCAACTAATGCGGTGTCGCTGGCGGCT___GAGGGCGGAGAGTTCTGTGGTGAAATAGTGG TGAG T GGPS1,TBCE Ensembl:ENSG00000152904,Ensembl:ENSG00000285053 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:235328496..235329066 26863196 MeRIP-seq:(Medium) rs1334982422 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1665,Human_RBP_ID_224214,Human_RBP_ID_346750,Human_RBP_ID_4074869,Human_RBP_ID_5413736,Human_RBP_ID_5433782,Human_RBP_ID_5457284,Human_RBP_ID_5485762,Human_RBP_ID_5784322,Human_RBP_ID_10853438,Human_RBP_ID_18415159,Human_RBP_ID_23375405 86341 RMVar_ID_86341 Human_SNP_ID_54304038 m1A Human chr1 + 235329399 235329399 235329399 GCGCCTGGTGAGACGGACAGATGCTGAACAAAACGATGTGAAATTACCGCAGTGGCAGTGCCCCA GCGCCTGGTGAGACGGACAGATGCTGAACAAAGCGATGTGAAATTACCGCAGTGGCAGTGCCCCA A G GGPS1,TBCE Ensembl:ENSG00000152904,Ensembl:ENSG00000285053 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:235329396..235329621 26863196 MeRIP-seq:(Medium) rs367668821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1425008 86342 RMVar_ID_86342 Human_SNP_ID_54307727 m1A Human chr1 + 235342960 235342957 235342961 CCTCTGTACAGATAATCAAAATTCAAAGTTGAAAGAATCAAAAGCAGCCACAGTTATGTAGGTCT CCTCTGTACAGATAATCAAAATTCAAAGTT____GAATCAAAAGCAGCCACAGTTATGTAGGTCT TGAAA T GGPS1,TBCE Ensembl:ENSG00000152904,Ensembl:ENSG00000285053 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:235342850..235342999 32194978 MeRIP-seq:(Medium) rs1316706338 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4034621,Human_RBP_ID_5784448,Human_RBP_ID_18567414,Human_RBP_ID_21879553 Human_miRNA_ID_2358822 RMVar_hsa_circ_140708,RMVar_hsa_circ_115113,RMVar_hsa_circ_266853,RMVar_hsa_circ_140711 86343 RMVar_ID_86343 Human_SNP_ID_54333077 m1A Human chr1 + 235437466 235437466 235437466 TCGCCAGCATTGGCCAGCTGAAGACGCTGAACAAATGTGAGGTGAGCACTGGCGTCATGACTAGA TCGCCAGCATTGGCCAGCTGAAGACGCTGAACTAATGTGAGGTGAGCACTGGCGTCATGACTAGA A T TBCE,TBCE:2 Ensembl:ENSG00000284770,Ensembl:ENSG00000285053 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:235436590..235438894 32194978 MeRIP-seq:(Medium) rs1450344942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19036081,Human_RBP_ID_23375578 Human_Splice_Rec_200511,Human_Splice_Rec_200549,Human_Splice_Rec_200591,Human_Splice_Rec_200635,Human_Splice_Rec_200671,Human_Splice_Rec_200707,Human_Splice_Rec_200745,Human_Splice_Rec_200783,Human_Splice_Rec_200815,Human_Splice_Rec_200849,Human_Splice_Rec_200907,Human_Splice_Rec_200963,Human_Splice_Rec_201005,Human_Splice_Rec_201041,Human_Splice_Rec_201075,Human_Splice_Rec_201107,Human_Splice_Rec_201133,Human_Splice_Rec_201167,Human_Splice_Rec_201199,Human_Splice_Rec_201231,Human_Splice_Rec_201263,Human_Splice_Rec_201293,Human_Splice_Rec_201323,Human_Splice_Rec_201373,Human_Splice_Rec_201403,Human_Splice_Rec_201435,Human_Splice_Rec_201499,Human_Splice_Rec_201531,Human_Splice_Rec_201563,Human_Splice_Rec_201593,Human_Splice_Rec_201625,Human_Splice_Rec_201657,Human_Splice_Rec_201687,Human_Splice_Rec_201715,Human_Splice_Rec_201741,Human_Splice_Rec_201775,Human_Splice_Rec_201805,Human_Splice_Rec_201831,Human_Splice_Rec_201863,Human_Splice_Rec_201893,Human_Splice_Rec_201921,Human_Splice_Rec_201945,Human_Splice_Rec_201967,Human_Splice_Rec_201989,Human_Splice_Rec_202011,Human_Splice_Rec_202031,Human_Splice_Rec_202057,Human_Splice_Rec_202087,Human_Splice_Rec_202123,Human_Splice_Rec_202147,Human_Splice_Rec_202175,Human_Splice_Rec_202189,Human_Splice_Rec_202211,Human_Splice_Rec_202229,Human_Splice_Rec_202243 RMVar_hsa_circ_25310,RMVar_hsa_circ_21744,RMVar_hsa_circ_314843,RMVar_hsa_circ_70967,RMVar_hsa_circ_331478,RMVar_hsa_circ_15289,RMVar_hsa_circ_319435,RMVar_hsa_circ_350466,RMVar_hsa_circ_317266,RMVar_hsa_circ_29401,RMVar_hsa_circ_140720,RMVar_hsa_circ_140721,RMVar_hsa_circ_11762,RMVar_hsa_circ_69609,RMVar_hsa_circ_342463,RMVar_hsa_circ_342105,RMVar_hsa_circ_73946,RMVar_hsa_circ_140724,RMVar_hsa_circ_321393,RMVar_hsa_circ_11683,RMVar_hsa_circ_336145,RMVar_hsa_circ_279972,RMVar_hsa_circ_140727,RMVar_hsa_circ_140728,RMVar_hsa_circ_140732,RMVar_hsa_circ_140736,RMVar_hsa_circ_324615,RMVar_hsa_circ_310284,RMVar_hsa_circ_140730,RMVar_hsa_circ_140731,RMVar_hsa_circ_351592,RMVar_hsa_circ_338646,RMVar_hsa_circ_298492,RMVar_hsa_circ_302904,RMVar_hsa_circ_275531,RMVar_hsa_circ_140734,RMVar_hsa_circ_140735,RMVar_hsa_circ_140733 86344 RMVar_ID_86344 Human_SNP_ID_54347110 m1A Human chr1 - 235489770 235489768 235489770 AAGGAAGGATGGAAGGTGAAGAGAATAATTAGAGTCAGGACTTTATCATGTTTGTAATGTGGAGG AAGGAAGGATGGAAGGTGAAGAGAATAATTAG__TCAGGACTTTATCATGTTTGTAATGTGGAGG ACT A B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:235489738..235489803 26863196 MeRIP-seq:(Medium) rs1228039024 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1153142,Human_RBP_ID_5785119,Human_RBP_ID_9560640,Human_RBP_ID_10856161,Human_RBP_ID_23375677 RMVar_hsa_circ_352347,RMVar_hsa_circ_357673,RMVar_hsa_circ_59735,RMVar_hsa_circ_297446,RMVar_hsa_circ_270881,RMVar_hsa_circ_281456,RMVar_hsa_circ_320504 86345 RMVar_ID_86345 Human_SNP_ID_54347612 m1A Human chr1 - 235491818 235491818 235491818 TAGGAGAGTAGAGAGGTGTATATAAAGAAAAGAGGGGGGAAGCATATGACTGTGAGAGGCAGACA TAGGAGAGTAGAGAGGTGTATATAAAGAAAAGGGGGGGGAAGCATATGACTGTGAGAGGCAGACA T C B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:235491776..235491858 26863196 MeRIP-seq:(Medium) rs969013002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8965533,Human_RBP_ID_9560654,Human_RBP_ID_22858003 RMVar_hsa_circ_352347,RMVar_hsa_circ_357673,RMVar_hsa_circ_59735,RMVar_hsa_circ_297446,RMVar_hsa_circ_270881,RMVar_hsa_circ_281456,RMVar_hsa_circ_320504 86346 RMVar_ID_86346 Human_SNP_ID_54351082 m1A Human chr1 - 235505330 235505330 235505330 TCGTTCTCATCCTTCTCTCCCATCCTCACCCCAGTGCCTTCACCGCCCCGTCCCCGCTTTCCGGC TCGTTCTCATCCTTCTCTCCCATCCTCACCCCGGTGCCTTCACCGCCCCGTCCCCGCTTTCCGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:235505045..235505395 26863196 MeRIP-seq:(Medium) rs369226688 Functional Loss SNV dbSNP153 33..33 33 - - - 86347 RMVar_ID_86347 Human_SNP_ID_54388556 m1A Human chr1 - 235649732 235649732 235649732 CCCGAGCCCGGCCCGCGCCCCGATGCGGAGCGATGCCGCTCGGCCTGGCCGCCCCCCGCGAGCAC CCCGAGCCCGGCCCGCGCCCCGATGCGGAGCGTTGCCGCTCGGCCTGGCCGCCCCCCGCGAGCAC T A GNG4 Ensembl:ENSG00000168243 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1465441497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347048,Human_RBP_ID_3330595,Human_RBP_ID_4076492 Human_Splice_Rec_202339 86348 RMVar_ID_86348 Human_SNP_ID_54388604 m1A Human chr1 + 235649855 235649855 235649855 GGCCCCGCCCCGCGCCGCGCCTCCCGCCCTGCAGGGCCCGACCACGCGGGCCTGGGGGCGCAGGC GGCCCCGCCCCGCGCCGCGCCTCCCGCCCTGCGGGGCCCGACCACGCGGGCCTGGGGGCGCAGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:235649808..235649998 26863196 MeRIP-seq:(Medium) rs1051690027 Functional Loss SNV dbSNP153 33..33 33 - - - 86349 RMVar_ID_86349 Human_SNP_ID_54509963 m1A Human chr1 + 236142691 236142691 236142691 CCCGGCCCGATGGAGACCCCGCCGTGGGACCCAGCCCGCAACGACTCGCTGCCGCCCACGCTGAC CCCGGCCCGATGGAGACCCCGCCGTGGGACCCGGCCCGCAACGACTCGCTGCCGCCCACGCTGAC A G GPR137B Ensembl:ENSG00000077585 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:236142595..236142751 26863410 MeRIP-seq:(Medium) rs925227661 Functional Loss SNV dbSNP153 33..33 33 - - - 86350 RMVar_ID_86350 Human_SNP_ID_54509999 m1A Human chr1 - 236142751 236142751 236142751 GCGTAGAACACGGTGTAGACGACGGTGAGGCCAAGCTTCACGTAGGGGGGCACGGCCGGGGTCAG GCGTAGAACACGGTGTAGACGACGGTGAGGCCCAGCTTCACGTAGGGGGGCACGGCCGGGGTCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:236142569..236142833 26863196 MeRIP-seq:(Medium) rs1051852177 Functional Loss SNV dbSNP153 33..33 33 - - - 86351 RMVar_ID_86351 Human_SNP_ID_54545469 m1A Human chr1 - 236281776 236281776 236281776 GGCCGCGGTGTGGGTAGAGGTCAGCATGAGCCAAGGGGTCCGCCGGGCAGGCGCTGGGCAGGGGG GGCCGCGGTGTGGGTAGAGGTCAGCATGAGCCGAGGGGTCCGCCGGGCAGGCGCTGGGCAGGGGG T C ERO1B Ensembl:ENSG00000086619 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:236281728..236281934 26863196 MeRIP-seq:(Medium) rs1248124877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347533,Human_RBP_ID_4073355 Human_Splice_Rec_202813 86352 RMVar_ID_86352 Human_SNP_ID_54616252 m1A Human chr1 - 236554626 236554626 236554626 TACCCAGCATTTTATAAGTAAAGAGAGAGCAGAAGCCTTGATGATGCCTCTGGTGGATCAGGTAA TACCCAGCATTTTATAAGTAAAGAGAGAGCAGGAGCCTTGATGATGCCTCTGGTGGATCAGGTAA T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2275687 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_853321,Human_RBP_ID_9271868 Human_Splice_Rec_203335,Human_Splice_Rec_203421 GWAS_ID_10328,GWAS_ID_10329,GWAS_ID_10330,GWAS_ID_10331,GWAS_ID_10332,GWAS_ID_10333,GWAS_ID_10334,GWAS_ID_10335,GWAS_ID_10336,GWAS_ID_10337,GWAS_ID_10338,GWAS_ID_10339,GWAS_ID_10340,GWAS_ID_10341,GWAS_ID_10342,GWAS_ID_10343,GWAS_ID_10344,GWAS_ID_10345,GWAS_ID_10346,GWAS_ID_10347,GWAS_ID_10348,GWAS_ID_10349,GWAS_ID_10350,GWAS_ID_10351,GWAS_ID_10352,GWAS_ID_10353,GWAS_ID_10354,GWAS_ID_10355,GWAS_ID_10356,GWAS_ID_10357,GWAS_ID_10358,GWAS_ID_10359,GWAS_ID_10360,GWAS_ID_10361,GWAS_ID_10362,GWAS_ID_10363,GWAS_ID_10364,GWAS_ID_10365,GWAS_ID_10366,GWAS_ID_10367,GWAS_ID_10368,GWAS_ID_10369,GWAS_ID_10370,GWAS_ID_10371,GWAS_ID_10372,GWAS_ID_10373,GWAS_ID_10374,GWAS_ID_10375,GWAS_ID_10376,GWAS_ID_10377,GWAS_ID_10378,GWAS_ID_10379,GWAS_ID_10380,GWAS_ID_10381,GWAS_ID_10382,GWAS_ID_10383,GWAS_ID_10384,GWAS_ID_10385,GWAS_ID_10386,GWAS_ID_10387,GWAS_ID_10388,GWAS_ID_10389,GWAS_ID_10390,GWAS_ID_10391,GWAS_ID_10392,GWAS_ID_10393,GWAS_ID_10394,GWAS_ID_10395,GWAS_ID_10396,GWAS_ID_10397,GWAS_ID_10398,GWAS_ID_10399,GWAS_ID_10400,GWAS_ID_10401,GWAS_ID_10402,GWAS_ID_10403,GWAS_ID_10404,GWAS_ID_10405,GWAS_ID_10406,GWAS_ID_10407,GWAS_ID_10408,GWAS_ID_10409,GWAS_ID_10410,GWAS_ID_10411,GWAS_ID_10412,GWAS_ID_10413,GWAS_ID_10414,GWAS_ID_10415,GWAS_ID_10416,GWAS_ID_10417,GWAS_ID_10418,GWAS_ID_10419,GWAS_ID_10420,GWAS_ID_10421,GWAS_ID_10422,GWAS_ID_10423,GWAS_ID_10424,GWAS_ID_10425,GWAS_ID_10426,GWAS_ID_10427,GWAS_ID_10428,GWAS_ID_10429,GWAS_ID_10430,GWAS_ID_10431,GWAS_ID_10432,GWAS_ID_10433,GWAS_ID_10434,GWAS_ID_10435,GWAS_ID_10436,GWAS_ID_10437,GWAS_ID_10438,GWAS_ID_10439,GWAS_ID_10440,GWAS_ID_10441,GWAS_ID_10442,GWAS_ID_10443,GWAS_ID_10444,GWAS_ID_10445,GWAS_ID_10446,GWAS_ID_10447,GWAS_ID_10448,GWAS_ID_10449,GWAS_ID_10450,GWAS_ID_10451,GWAS_ID_10452,GWAS_ID_10453,GWAS_ID_10454,GWAS_ID_10455,GWAS_ID_10456,GWAS_ID_10457,GWAS_ID_10458,GWAS_ID_10459,GWAS_ID_10460,GWAS_ID_10461,GWAS_ID_10462,GWAS_ID_10463,GWAS_ID_10464,GWAS_ID_10465,GWAS_ID_10466,GWAS_ID_10467,GWAS_ID_10468,GWAS_ID_10469,GWAS_ID_10470,GWAS_ID_10471,GWAS_ID_10472,GWAS_ID_10473,GWAS_ID_10474,GWAS_ID_10475,GWAS_ID_10476,GWAS_ID_10477,GWAS_ID_10478,GWAS_ID_10479,GWAS_ID_10480,GWAS_ID_10481,GWAS_ID_10482,GWAS_ID_10483,GWAS_ID_10484,GWAS_ID_10485,GWAS_ID_10486,GWAS_ID_10487,GWAS_ID_10488,GWAS_ID_10489,GWAS_ID_10490,GWAS_ID_10491,GWAS_ID_10492,GWAS_ID_10493,GWAS_ID_10494,GWAS_ID_10495,GWAS_ID_10496,GWAS_ID_10497,GWAS_ID_10498,GWAS_ID_10499,GWAS_ID_10500,GWAS_ID_10501,GWAS_ID_10502,GWAS_ID_10503,GWAS_ID_10504,GWAS_ID_10505,GWAS_ID_10506,GWAS_ID_10507,GWAS_ID_10508,GWAS_ID_10509,GWAS_ID_10510,GWAS_ID_10511,GWAS_ID_10512,GWAS_ID_10513,GWAS_ID_10514,GWAS_ID_10515,GWAS_ID_10516,GWAS_ID_10517,GWAS_ID_10518,GWAS_ID_10519,GWAS_ID_10520,GWAS_ID_10521,GWAS_ID_10522,GWAS_ID_10523,GWAS_ID_10524,GWAS_ID_10525,GWAS_ID_10526,GWAS_ID_10527,GWAS_ID_10528,GWAS_ID_10529,GWAS_ID_10530,GWAS_ID_10531,GWAS_ID_10532,GWAS_ID_10533,GWAS_ID_10534,GWAS_ID_10535,GWAS_ID_10536,GWAS_ID_10537,GWAS_ID_10538,GWAS_ID_10539,GWAS_ID_10540,GWAS_ID_10541,GWAS_ID_10542,GWAS_ID_10543,GWAS_ID_10544,GWAS_ID_10545,GWAS_ID_10546,GWAS_ID_10547,GWAS_ID_10548,GWAS_ID_10549 RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_61188,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840 86353 RMVar_ID_86353 Human_SNP_ID_54616628 m1A Human chr1 - 236555835 236555835 236555835 CATCAGTCTCAGCTAACCGCCTTTTTCCTGGAAGCCCTGGACTTCCGAGCCCAGCACTCTGAGGT CATCAGTCTCAGCTAACCGCCTTTTTCCTGGAGGCCCTGGACTTCCGAGCCCAGCACTCTGAGGT T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1885532 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_221621,Human_RBP_ID_3937516,Human_RBP_ID_8754489,Human_RBP_ID_9271869,Human_RBP_ID_9357684,Human_RBP_ID_18966545,Human_RBP_ID_26767646 Human_Splice_Rec_203329,Human_Splice_Rec_203415 RMVar_hsa_circ_4051,RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_61188,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840,RMVar_hsa_circ_336753,RMVar_hsa_circ_374278,RMVar_hsa_circ_120373,RMVar_hsa_circ_140843,RMVar_hsa_circ_140844,RMVar_hsa_circ_140845 86354 RMVar_ID_86354 Human_SNP_ID_54616664 m1A Human chr1 + 236555932 236555932 236555932 TATGCTCTTGCAAGATGCTCATAAACGGACCCATGTGATTCTACCAATAACACAGGAAAGAGATG TATGCTCTTGCAAGATGCTCATAAACGGACCCGTGTGATTCTACCAATAACACAGGAAAGAGATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:236555882..236555964 26863196 MeRIP-seq:(Medium) rs370868615 Functional Loss SNV dbSNP153 33..33 33 - - - 86355 RMVar_ID_86355 Human_SNP_ID_54619471 m1A Human chr1 - 236566007 236566007 236566007 ATTTTAGAAGCAGACACTGAATTTTGGTTTTCAGTCTGTTGTGAGTTTAGTGTCCAGCATCAGAT ATTTTAGAAGCAGACACTGAATTTTGGTTTTCGGTCTGTTGTGAGTTTAGTGTCCAGCATCAGAT T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:236564613..236566821 32194978 MeRIP-seq:(Medium) rs375051087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19053,Human_RBP_ID_1741708,Human_RBP_ID_3304432,Human_RBP_ID_18567897,Human_RBP_ID_23376561 Human_Splice_Rec_203312,Human_Splice_Rec_203313,Human_Splice_Rec_203398,Human_Splice_Rec_203399 RMVar_hsa_circ_275,RMVar_hsa_circ_4051,RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840,RMVar_hsa_circ_120373,RMVar_hsa_circ_17969,RMVar_hsa_circ_140845,RMVar_hsa_circ_21340,RMVar_hsa_circ_64336,RMVar_hsa_circ_140846,RMVar_hsa_circ_316425,RMVar_hsa_circ_336589,RMVar_hsa_circ_27638,RMVar_hsa_circ_4802 86356 RMVar_ID_86356 Human_SNP_ID_54622083 m1A Human chr1 - 236574806 236574806 236574806 AGCTGTGCTGAAAGATGAGGCCATGGTTCTGCATCTCACTCTGGGAAAGTATAATGAATTTTCAG AGCTGTGCTGAAAGATGAGGCCATGGTTCTGCGTCTCACTCTGGGAAAGTATAATGAATTTTCAG T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:236574755..236574833 32194978 MeRIP-seq:(Medium) rs1380599136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1741748,Human_RBP_ID_5787444,Human_RBP_ID_8303872,Human_RBP_ID_8746120,Human_RBP_ID_10861051,Human_RBP_ID_18567923,Human_RBP_ID_24663440,Human_RBP_ID_27590721 Human_Splice_Rec_203296 RMVar_hsa_circ_275,RMVar_hsa_circ_123102,RMVar_hsa_circ_140842,RMVar_hsa_circ_21340,RMVar_hsa_circ_64336,RMVar_hsa_circ_27638,RMVar_hsa_circ_53000,RMVar_hsa_circ_101371,RMVar_hsa_circ_47762,RMVar_hsa_circ_140848,RMVar_hsa_circ_332732,RMVar_hsa_circ_363266,RMVar_hsa_circ_125877,RMVar_hsa_circ_140851,RMVar_hsa_circ_97588,RMVar_hsa_circ_140853,RMVar_hsa_circ_140852,RMVar_hsa_circ_140849,RMVar_hsa_circ_140850,RMVar_hsa_circ_94604,RMVar_hsa_circ_32223,RMVar_hsa_circ_7905,RMVar_hsa_circ_49929,RMVar_hsa_circ_140855,RMVar_hsa_circ_54422,RMVar_hsa_circ_140856 86357 RMVar_ID_86357 Human_SNP_ID_54630386 m1A Human chr1 + 236604106 236604106 236604106 GCTGCTGGGCTAAGGACGTCATCTTTCACGCCAGCGGAGTTTTAATGACACGGGCTAAAAAAACG GCTGCTGGGCTAAGGACGTCATCTTTCACGCCTGCGGAGTTTTAATGACACGGGCTAAAAAAACG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:236604059..236604140 26863196 MeRIP-seq:(Medium) rs755825480 Functional Loss SNV dbSNP153 33..33 33 - - - 86358 RMVar_ID_86358 Human_SNP_ID_54679513 m1A Human chr1 + 236795485 236795485 236795485 GGCCGGGTACCCGGGAAGAAAGCACGTGCTCCAGCAGTTGCCGCGCCCAGCCCCGAGAGAGGCCC GGCCGGGTACCCGGGAAGAAAGCACGTGCTCCGGCAGTTGCCGCGCCCAGCCCCGAGAGAGGCCC A G MTR Ensembl:ENSG00000116984 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:236795369..236795502 26863196 MeRIP-seq:(Medium) rs1431838478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4035887,Human_RBP_ID_9271889,Human_RBP_ID_18429855,Human_RBP_ID_22026597,Human_RBP_ID_22431335 86359 RMVar_ID_86359 Human_SNP_ID_54691246 m1A Human chr1 + 236843808 236843808 236843808 CTGTTGGCTTGGGCAATTGAAAGGAAGGAGCTACTGAGGTAAGAAAGACTGAGAAGCAGGTTTGG CTGTTGGCTTGGGCAATTGAAAGGAAGGAGCTGCTGAGGTAAGAAAGACTGAGAAGCAGGTTTGG A G MTR Ensembl:ENSG00000116984 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:236843803..236843911 26863196 MeRIP-seq:(Medium) rs1293913547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10863151 RMVar_hsa_circ_15088,RMVar_hsa_circ_355569,RMVar_hsa_circ_373574,RMVar_hsa_circ_378083,RMVar_hsa_circ_339919,RMVar_hsa_circ_349142,RMVar_hsa_circ_308986,RMVar_hsa_circ_300103,RMVar_hsa_circ_55526,RMVar_hsa_circ_140886,RMVar_hsa_circ_28167,RMVar_hsa_circ_140887,RMVar_hsa_circ_140888,RMVar_hsa_circ_140885,RMVar_hsa_circ_317102,RMVar_hsa_circ_273935,RMVar_hsa_circ_59094,RMVar_hsa_circ_70698,RMVar_hsa_circ_16026,RMVar_hsa_circ_2641,RMVar_hsa_circ_21489,RMVar_hsa_circ_34150,RMVar_hsa_circ_140889,RMVar_hsa_circ_287899,RMVar_hsa_circ_372572,RMVar_hsa_circ_60763,RMVar_hsa_circ_140894,RMVar_hsa_circ_140895,RMVar_hsa_circ_362079,RMVar_hsa_circ_264935,RMVar_hsa_circ_140897,RMVar_hsa_circ_337849,RMVar_hsa_circ_140901,RMVar_hsa_circ_93058,RMVar_hsa_circ_35173,RMVar_hsa_circ_294017,RMVar_hsa_circ_312529,RMVar_hsa_circ_15701,RMVar_hsa_circ_140903,RMVar_hsa_circ_140902,RMVar_hsa_circ_9558,RMVar_hsa_circ_33168,RMVar_hsa_circ_346239,RMVar_hsa_circ_372369,RMVar_hsa_circ_8166,RMVar_hsa_circ_122385,RMVar_hsa_circ_47052,RMVar_hsa_circ_371125,RMVar_hsa_circ_140909,RMVar_hsa_circ_378890,RMVar_hsa_circ_320199,RMVar_hsa_circ_275108,RMVar_hsa_circ_140911,RMVar_hsa_circ_140913,RMVar_hsa_circ_140914,RMVar_hsa_circ_140912,RMVar_hsa_circ_140910,RMVar_hsa_circ_335432,RMVar_hsa_circ_140916,RMVar_hsa_circ_140915 86360 RMVar_ID_86360 Human_SNP_ID_54691255 m1A Human chr1 + 236843830 236843830 236843830 GGAAGGAGCTACTGAGGTAAGAAAGACTGAGAAGCAGGTTTGGGATGGGGTAAGGAGAAGTTTGG GGAAGGAGCTACTGAGGTAAGAAAGACTGAGAGGCAGGTTTGGGATGGGGTAAGGAGAAGTTTGG A G MTR Ensembl:ENSG00000116984 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:236843808..236843937 26863196 MeRIP-seq:(Medium) rs1407772864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23376883 RMVar_hsa_circ_15088,RMVar_hsa_circ_355569,RMVar_hsa_circ_373574,RMVar_hsa_circ_378083,RMVar_hsa_circ_339919,RMVar_hsa_circ_349142,RMVar_hsa_circ_308986,RMVar_hsa_circ_300103,RMVar_hsa_circ_55526,RMVar_hsa_circ_140886,RMVar_hsa_circ_28167,RMVar_hsa_circ_140887,RMVar_hsa_circ_140888,RMVar_hsa_circ_140885,RMVar_hsa_circ_317102,RMVar_hsa_circ_273935,RMVar_hsa_circ_59094,RMVar_hsa_circ_70698,RMVar_hsa_circ_16026,RMVar_hsa_circ_2641,RMVar_hsa_circ_21489,RMVar_hsa_circ_34150,RMVar_hsa_circ_140889,RMVar_hsa_circ_287899,RMVar_hsa_circ_372572,RMVar_hsa_circ_60763,RMVar_hsa_circ_140894,RMVar_hsa_circ_140895,RMVar_hsa_circ_362079,RMVar_hsa_circ_264935,RMVar_hsa_circ_140897,RMVar_hsa_circ_337849,RMVar_hsa_circ_140901,RMVar_hsa_circ_93058,RMVar_hsa_circ_35173,RMVar_hsa_circ_294017,RMVar_hsa_circ_312529,RMVar_hsa_circ_15701,RMVar_hsa_circ_140903,RMVar_hsa_circ_140902,RMVar_hsa_circ_9558,RMVar_hsa_circ_33168,RMVar_hsa_circ_346239,RMVar_hsa_circ_372369,RMVar_hsa_circ_8166,RMVar_hsa_circ_122385,RMVar_hsa_circ_47052,RMVar_hsa_circ_371125,RMVar_hsa_circ_140909,RMVar_hsa_circ_378890,RMVar_hsa_circ_320199,RMVar_hsa_circ_275108,RMVar_hsa_circ_140911,RMVar_hsa_circ_140913,RMVar_hsa_circ_140914,RMVar_hsa_circ_140912,RMVar_hsa_circ_140910,RMVar_hsa_circ_335432,RMVar_hsa_circ_140916,RMVar_hsa_circ_140915 86361 RMVar_ID_86361 Human_SNP_ID_54704806 m1A Human chr1 + 236897756 236897756 236897756 ACAAAAAACCTGTGTGCATCTGGCTGACACTTACCTGCTTCTGGTTTTCGAAGACTATTTAGTGG ACAAAAAACCTGTGTGCATCTGGCTGACACTTCCCTGCTTCTGGTTTTCGAAGACTATTTAGTGG A C MTR Ensembl:ENSG00000116984 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2853522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8746208,Human_RBP_ID_10864143,Human_RBP_ID_26377365,Human_RBP_ID_27178852 Human_miRNA_ID_821712 Clinvar_Rec_459,Clinvar_Rec_460,Clinvar_Rec_461,Clinvar_Rec_462 GWAS_ID_10550,GWAS_ID_10551,GWAS_ID_10552,GWAS_ID_10553,GWAS_ID_10554,GWAS_ID_10555,GWAS_ID_10556,GWAS_ID_10557,GWAS_ID_10558,GWAS_ID_10559,GWAS_ID_10560,GWAS_ID_10561,GWAS_ID_10562,GWAS_ID_10563,GWAS_ID_10564,GWAS_ID_10565,GWAS_ID_10566,GWAS_ID_10567,GWAS_ID_10568,GWAS_ID_10569,GWAS_ID_10570,GWAS_ID_10571,GWAS_ID_10572,GWAS_ID_10573,GWAS_ID_10574,GWAS_ID_10575,GWAS_ID_10576,GWAS_ID_10577,GWAS_ID_10578,GWAS_ID_10579,GWAS_ID_10580,GWAS_ID_10581,GWAS_ID_10582,GWAS_ID_10583,GWAS_ID_10584,GWAS_ID_10585,GWAS_ID_10586,GWAS_ID_10587,GWAS_ID_10588,GWAS_ID_10589,GWAS_ID_10590,GWAS_ID_10591,GWAS_ID_10592,GWAS_ID_10593,GWAS_ID_10594,GWAS_ID_10595,GWAS_ID_10596 86362 RMVar_ID_86362 Human_SNP_ID_54704807 m1A Human chr1 + 236897756 236897756 236897756 ACAAAAAACCTGTGTGCATCTGGCTGACACTTACCTGCTTCTGGTTTTCGAAGACTATTTAGTGG ACAAAAAACCTGTGTGCATCTGGCTGACACTTTCCTGCTTCTGGTTTTCGAAGACTATTTAGTGG A T MTR Ensembl:ENSG00000116984 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2853522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8746208,Human_RBP_ID_10864143,Human_RBP_ID_26377365,Human_RBP_ID_27178852 Human_miRNA_ID_821712 Clinvar_Rec_459,Clinvar_Rec_460,Clinvar_Rec_461,Clinvar_Rec_462 GWAS_ID_10550,GWAS_ID_10551,GWAS_ID_10552,GWAS_ID_10553,GWAS_ID_10554,GWAS_ID_10555,GWAS_ID_10556,GWAS_ID_10557,GWAS_ID_10558,GWAS_ID_10559,GWAS_ID_10560,GWAS_ID_10561,GWAS_ID_10562,GWAS_ID_10563,GWAS_ID_10564,GWAS_ID_10565,GWAS_ID_10566,GWAS_ID_10567,GWAS_ID_10568,GWAS_ID_10569,GWAS_ID_10570,GWAS_ID_10571,GWAS_ID_10572,GWAS_ID_10573,GWAS_ID_10574,GWAS_ID_10575,GWAS_ID_10576,GWAS_ID_10577,GWAS_ID_10578,GWAS_ID_10579,GWAS_ID_10580,GWAS_ID_10581,GWAS_ID_10582,GWAS_ID_10583,GWAS_ID_10584,GWAS_ID_10585,GWAS_ID_10586,GWAS_ID_10587,GWAS_ID_10588,GWAS_ID_10589,GWAS_ID_10590,GWAS_ID_10591,GWAS_ID_10592,GWAS_ID_10593,GWAS_ID_10594,GWAS_ID_10595,GWAS_ID_10596 86363 RMVar_ID_86363 Human_SNP_ID_54705461 m1A Human chr1 + 236900204 236900204 236900204 CTACAGGAAAATAGGTGAATAATTAGATATATATATTCATTCTACGGGATATTATTCAGTAGTGG CTACAGGAAAATAGGTGAATAATTAGATATATGTATTCATTCTACGGGATATTATTCAGTAGTGG A G MTR Ensembl:ENSG00000116984 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347687,Human_RBP_ID_2135032,Human_RBP_ID_26390671,Human_RBP_ID_27178886,Human_RBP_ID_27590812 Human_miRNA_ID_149554 Clinvar_Rec_463 86364 RMVar_ID_86364 Human_SNP_ID_54778468 m1A Human chr1 - 237194403 237194403 237194403 TCCCACACGGGAATCTCAGAGGCTGCACTATGAGCTCCTTGCCGCTGTTTCTCACTCATGTATAG TCCCACACGGGAATCTCAGAGGCTGCACTATGGGCTCCTTGCCGCTGTTTCTCACTCATGTATAG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:237194394..237194507 26863196 MeRIP-seq:(Medium) rs1422640143 Functional Loss SNV dbSNP153 33..33 33 - - - 86365 RMVar_ID_86365 Human_SNP_ID_54969361 m1A Human chr1 - 237944456 237944456 237944456 GAACTCTGCAAATCTTACTCGGCCTGTTTACCAAAAATATCTCCTCTAGCATTTCCAGTATTAGA GAACTCTGCAAATCTTACTCGGCCTGTTTACCGAAAATATCTCCTCTAGCATTTCCAGTATTAGA T C MTRNR2L11 Ensembl:ENSG00000270188 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:237944351..237944500 26863196 MeRIP-seq:(Medium) rs1320191371 Functional Loss SNV dbSNP153 33..33 33 - - - 86366 RMVar_ID_86366 Human_SNP_ID_54969373 m1A Human chr1 - 237944487 237944487 237944487 TGCTCTAAGGAAAGATTACAAAAAGTAAAAGGAACTCTGCAAATCTTACTCGGCCTGTTTACCAA TGCTCTAAGGAAAGATTACAAAAAGTAAAAGGTACTCTGCAAATCTTACTCGGCCTGTTTACCAA T A MTRNR2L11 Ensembl:ENSG00000270188 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:237944398..237944492 26863196 MeRIP-seq:(Medium) rs530361509 Functional Loss SNV dbSNP153 33..33 33 - - - 86367 RMVar_ID_86367 Human_SNP_ID_55297150 m1A Human chr1 - 239260739 239260739 239260739 GTGGTACATGCCTGTAATCCCAGCTAGTCAGGAGGCTGAGGAAGGAGAATCACTTGAACATGGAA GTGGTACATGCCTGTAATCCCAGCTAGTCAGGGGGCTGAGGAAGGAGAATCACTTGAACATGGAA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:239260711..239260798 26863410 MeRIP-seq:(Medium) rs983443153 Functional Loss SNV dbSNP153 33..33 33 - - - 86368 RMVar_ID_86368 Human_SNP_ID_107807781 m1A Human chr2 - 195657482 195657482 195657482 GAGGAGCCGCGGCGCCCAACACTCTGCCCACCACGCGCTCTGCTTCGGCTGGCCGCCGCCGACTG GAGGAGCCGCGGCGCCCAACACTCTGCCCACCGCGCGCTCTGCTTCGGCTGGCCGCCGCCGACTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:195657270..195657716 26863196 MeRIP-seq:(Medium) rs1416348968 Functional Loss SNV dbSNP153 33..33 33 - - - 86369 RMVar_ID_86369 Human_SNP_ID_107807982 m1A Human chr2 - 195657969 195657969 195657969 ACCGACCCGGCCCCACCCTCACCCTCAGCTCCAGGGACCCCCAGCAGGCCGAGATCTTCACACCC ACCGACCCGGCCCCACCCTCACCCTCAGCTCCGGGGACCCCCAGCAGGCCGAGATCTTCACACCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:195657951..195658150 26863196 MeRIP-seq:(Medium) rs1286660559 Functional Loss SNV dbSNP153 33..33 33 - - - 86370 RMVar_ID_86370 Human_SNP_ID_107808037 m1A Human chr2 + 195658106 195658106 195658106 ATGTGGGGCGCGGCAGGGGGATCGCGTAGAGGAACCTTCGCGCACCGCCTCTCCGGGTCTGGGAA ATGTGGGGCGCGGCAGGGGGATCGCGTAGAGGGACCTTCGCGCACCGCCTCTCCGGGTCTGGGAA A G SLC39A10 Ensembl:ENSG00000196950 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:195658058..195658229 26863196 MeRIP-seq:(Medium) rs1487431557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2612171,Human_RBP_ID_3638245,Human_RBP_ID_5196589,Human_RBP_ID_5322254,Human_RBP_ID_8110400,Human_RBP_ID_8200764 Human_Splice_Rec_340428 86371 RMVar_ID_86371 Human_SNP_ID_107821829 m1A Human chr2 + 195716852 195716852 195716852 ACCACCACGGCGAGAACAAAACTGTGCTGAGGAAGCATAATCACCAGTGGCACCACAAGCATTCT ACCACCACGGCGAGAACAAAACTGTGCTGAGGCAGCATAATCACCAGTGGCACCACAAGCATTCT A C SLC39A10 Ensembl:ENSG00000196950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:195716801..195716875 26863196 MeRIP-seq:(Medium) rs1178506077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17697946,Human_RBP_ID_26820345 Human_miRNA_ID_2997575 RMVar_hsa_circ_287823,RMVar_hsa_circ_283209,RMVar_hsa_circ_205461,RMVar_hsa_circ_205462,RMVar_hsa_circ_107070,RMVar_hsa_circ_205465,RMVar_hsa_circ_205473,RMVar_hsa_circ_295668,RMVar_hsa_circ_370253,RMVar_hsa_circ_349102,RMVar_hsa_circ_89162,RMVar_hsa_circ_205470,RMVar_hsa_circ_205471,RMVar_hsa_circ_205469,RMVar_hsa_circ_69253,RMVar_hsa_circ_121545,RMVar_hsa_circ_205472,RMVar_hsa_circ_374047,RMVar_hsa_circ_205474,RMVar_hsa_circ_300686,RMVar_hsa_circ_317483,RMVar_hsa_circ_374249,RMVar_hsa_circ_205475 86372 RMVar_ID_86372 Human_SNP_ID_108066272 m1A Human chr2 + 196726961 196726961 196726961 GCATGAGTTTAGGAAGGTTAATGTAACAGCAGAGGACAGTAGAGGATAATGAAGAGAAACTGGAG GCATGAGTTTAGGAAGGTTAATGTAACAGCAGGGGACAGTAGAGGATAATGAAGAGAAACTGGAG A G CCDC150 Ensembl:ENSG00000144395 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:196726818..196726973;chr2:196726838..196726999 26863196 MeRIP-seq:(Medium) rs1318124360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62561,RMVar_hsa_circ_60209,RMVar_hsa_circ_56950,RMVar_hsa_circ_9406,RMVar_hsa_circ_61061 86373 RMVar_ID_86373 Human_SNP_ID_108082234 m1A Human chr2 - 196793037 196793037 196793037 GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAAGAAACACCTGAGCAACCCACTGCGGGCGATGT GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAAACACCTGAGCAACCCACTGCGGGCGATGT T C GTF3C3 Ensembl:ENSG00000119041 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:196792929..196793182 26863196 MeRIP-seq:(Medium) rs1431679197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58340,Human_RBP_ID_242651,Human_RBP_ID_829972,Human_RBP_ID_923706,Human_RBP_ID_9385238,Human_RBP_ID_21982413,Human_RBP_ID_22997213,Human_RBP_ID_24546546,Human_RBP_ID_26340188,Human_RBP_ID_27817894 Human_Splice_Rec_341327,Human_Splice_Rec_341361,Human_Splice_Rec_341417,Human_Splice_Rec_341443 RMVar_hsa_circ_98334,RMVar_hsa_circ_46649,RMVar_hsa_circ_205547,RMVar_hsa_circ_23316,RMVar_hsa_circ_61581,RMVar_hsa_circ_276527,RMVar_hsa_circ_205555,RMVar_hsa_circ_74775 86374 RMVar_ID_86374 Human_SNP_ID_108082235 m1A Human chr2 - 196793037 196793037 196793037 GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAAGAAACACCTGAGCAACCCACTGCGGGCGATGT GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGACGAAACACCTGAGCAACCCACTGCGGGCGATGT T G GTF3C3 Ensembl:ENSG00000119041 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:196792929..196793182 26863196 MeRIP-seq:(Medium) rs1431679197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58340,Human_RBP_ID_242651,Human_RBP_ID_829972,Human_RBP_ID_923706,Human_RBP_ID_9385238,Human_RBP_ID_21982413,Human_RBP_ID_22997213,Human_RBP_ID_24546546,Human_RBP_ID_26340188,Human_RBP_ID_27817894 Human_Splice_Rec_341327,Human_Splice_Rec_341361,Human_Splice_Rec_341417,Human_Splice_Rec_341443 RMVar_hsa_circ_98334,RMVar_hsa_circ_46649,RMVar_hsa_circ_205547,RMVar_hsa_circ_23316,RMVar_hsa_circ_61581,RMVar_hsa_circ_276527,RMVar_hsa_circ_205555,RMVar_hsa_circ_74775 86375 RMVar_ID_86375 Human_SNP_ID_108082237 m1A Human chr2 - 196793041 196793041 196793041 GGAAGAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAAGAAACACCTGAGCAACCCACTGCGGGCG GGAAGAGGAAGAAGAGGAGGAGGAGGAGGAGGCGGAAGAAACACCTGAGCAACCCACTGCGGGCG T G GTF3C3 Ensembl:ENSG00000119041 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:196792931..196793149 26863196 MeRIP-seq:(Medium) rs1437765008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58340,Human_RBP_ID_242651,Human_RBP_ID_829972,Human_RBP_ID_9385238,Human_RBP_ID_21982413,Human_RBP_ID_22997213,Human_RBP_ID_24546546,Human_RBP_ID_26340188,Human_RBP_ID_27817894 Human_Splice_Rec_341327,Human_Splice_Rec_341361,Human_Splice_Rec_341417,Human_Splice_Rec_341443 RMVar_hsa_circ_98334,RMVar_hsa_circ_46649,RMVar_hsa_circ_205547,RMVar_hsa_circ_23316,RMVar_hsa_circ_61581,RMVar_hsa_circ_276527,RMVar_hsa_circ_205555,RMVar_hsa_circ_74775 86376 RMVar_ID_86376 Human_SNP_ID_108082273 m1A Human chr2 - 196793151 196793151 196793151 ACCCCTCCCCCATCAATGTCTCTTTTCTCAGGAGAAACATCAGATGGAGTGAGGAAGTCAGTTCA ACCCCTCCCCCATCAATGTCTCTTTTCTCAGGCGAAACATCAGATGGAGTGAGGAAGTCAGTTCA T G GTF3C3 Ensembl:ENSG00000119041 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:196793103..196797848 32194978 MeRIP-seq:(Medium) rs1466855158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26341674,Human_RBP_ID_27817895 Human_Splice_Rec_341326,Human_Splice_Rec_341360,Human_Splice_Rec_341416,Human_Splice_Rec_341442,Human_Splice_Rec_341450,Human_Splice_Rec_341454 RMVar_hsa_circ_98334,RMVar_hsa_circ_46649,RMVar_hsa_circ_205547,RMVar_hsa_circ_23316,RMVar_hsa_circ_61581,RMVar_hsa_circ_276527,RMVar_hsa_circ_205555,RMVar_hsa_circ_74775 86377 RMVar_ID_86377 Human_SNP_ID_108083762 m1A Human chr2 + 196799463 196799463 196799463 AGCGGTCGTCTGGGTCCCCCACACCTAAGGGTATGAAGGCAACAAGAGTGAAGGGCACCGTGGCC AGCGGTCGTCTGGGTCCCCCACACCTAAGGGTGTGAAGGCAACAAGAGTGAAGGGCACCGTGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:196799457..196799639 26863196 MeRIP-seq:(Medium) rs1012383310 Functional Loss SNV dbSNP153 33..33 33 - - - 86378 RMVar_ID_86378 Human_SNP_ID_108112642 m1A Human chr2 + 196926629 196926620 196926629 TTAACTGAGTGAAGAAACATGGTGCCGCCACCACCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC TTAACTGAGTGAAGAAACATGGTG_________CCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC GCCGCCACCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:196926580..196926733;chr2:196926601..196926725 26863196 MeRIP-seq:(Medium) rs1210657379 Functional Loss DEL dbSNP153 25..33 33 - - - 86379 RMVar_ID_86379 Human_SNP_ID_108112650 m1A Human chr2 + 196926629 196926629 196926629 TTAACTGAGTGAAGAAACATGGTGCCGCCACCACCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC TTAACTGAGTGAAGAAACATGGTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:196926580..196926733;chr2:196926601..196926725 26863196 MeRIP-seq:(Medium) rs963651695 Functional Loss SNV dbSNP153 33..33 33 - - - 86380 RMVar_ID_86380 Human_SNP_ID_108112688 m1A Human chr2 + 196926693 196926685 196926694 CTTCTCCGCCGCGGGGCCCCAAGCCCGGACTGAGCGTGCTAGACACTGTCCGACCGCCACCCCCG CTTCTCCGCCGCGGGGCCCCAAGCC_________CGTGCTAGACACTGTCCGACCGCCACCCCCG CCGGACTGAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:196926568..196926733 26863196 MeRIP-seq:(Medium) rs1320646825 Functional Loss DEL dbSNP153 26..34 33 - - - 86381 RMVar_ID_86381 Human_SNP_ID_108112698 m1A Human chr2 + 196926693 196926693 196926693 CTTCTCCGCCGCGGGGCCCCAAGCCCGGACTGAGCGTGCTAGACACTGTCCGACCGCCACCCCCG CTTCTCCGCCGCGGGGCCCCAAGCCCGGACTGGGCGTGCTAGACACTGTCCGACCGCCACCCCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:196926568..196926733 26863196 MeRIP-seq:(Medium) rs1272752800 Functional Loss SNV dbSNP153 33..33 33 - - - 86382 RMVar_ID_86382 Human_SNP_ID_108215925 m1A Human chr2 - 197379900 197379900 197379900 ACACCAAGATCAAAAGGACAAGAATCCTTCAAAAAACAGGAAAAAACTCCTAAAACACCTAAAAG ACACCAAGATCAAAAGGACAAGAATCCTTCAAGAAACAGGAAAAAACTCCTAAAACACCTAAAAG T C NPM1P46 Ensembl:ENSG00000213104 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879111961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6962126 86383 RMVar_ID_86383 Human_SNP_ID_108218867 m1A Human chr2 + 197392423 197392419 197392423 GAACCAATGTAGATGGAGTTGTAAATTTTCCAATATACATCTCTGACTTTCCGGGCTGGGTGAAA GAACCAATGTAGATGGAGTTGTAAATTTT____TATACATCTCTGACTTTCCGGGCTGGGTGAAA TCCAA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:197392373..197393033 32194978 MeRIP-seq:(Medium) rs776254147 Functional Loss DEL dbSNP153 30..33 33 - - - 86384 RMVar_ID_86384 Human_SNP_ID_108221002 m1A Human chr2 - 197400934 197400934 197400934 AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTAGTTGATACTACTGTGGAGTTGGCAAACAAAGT AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTTGTTGATACTACTGTGGAGTTGGCAAACAAAGT T A SF3B1 Ensembl:ENSG00000115524 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:197400901..197400950 26863196 MeRIP-seq:(Medium) rs780559382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57610,Human_RBP_ID_4591016,Human_RBP_ID_5528137,Human_RBP_ID_6868908,Human_RBP_ID_8844489,Human_RBP_ID_18752075 Human_Splice_Rec_342072,Human_Splice_Rec_342120,Human_Splice_Rec_342168,Human_Splice_Rec_342214 RMVar_hsa_circ_67972,RMVar_hsa_circ_101657,RMVar_hsa_circ_110410,RMVar_hsa_circ_111095,RMVar_hsa_circ_107983,RMVar_hsa_circ_93312,RMVar_hsa_circ_92499,RMVar_hsa_circ_205639,RMVar_hsa_circ_205643,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_127502,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636,RMVar_hsa_circ_120089,RMVar_hsa_circ_123680,RMVar_hsa_circ_104933,RMVar_hsa_circ_86592,RMVar_hsa_circ_205649,RMVar_hsa_circ_205651,RMVar_hsa_circ_205652,RMVar_hsa_circ_205650,RMVar_hsa_circ_346958,RMVar_hsa_circ_82724,RMVar_hsa_circ_205654,RMVar_hsa_circ_205655,RMVar_hsa_circ_79158,RMVar_hsa_circ_40892,RMVar_hsa_circ_205656,RMVar_hsa_circ_3015,RMVar_hsa_circ_268639 86385 RMVar_ID_86385 Human_SNP_ID_108221003 m1A Human chr2 - 197400934 197400934 197400934 AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTAGTTGATACTACTGTGGAGTTGGCAAACAAAGT AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTGGTTGATACTACTGTGGAGTTGGCAAACAAAGT T C SF3B1 Ensembl:ENSG00000115524 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:197400901..197400950 26863196 MeRIP-seq:(Medium) rs780559382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57610,Human_RBP_ID_4591016,Human_RBP_ID_5528137,Human_RBP_ID_6868908,Human_RBP_ID_8844489,Human_RBP_ID_18752075 Human_Splice_Rec_342072,Human_Splice_Rec_342120,Human_Splice_Rec_342168,Human_Splice_Rec_342214 RMVar_hsa_circ_67972,RMVar_hsa_circ_101657,RMVar_hsa_circ_110410,RMVar_hsa_circ_111095,RMVar_hsa_circ_107983,RMVar_hsa_circ_93312,RMVar_hsa_circ_92499,RMVar_hsa_circ_205639,RMVar_hsa_circ_205643,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_127502,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636,RMVar_hsa_circ_120089,RMVar_hsa_circ_123680,RMVar_hsa_circ_104933,RMVar_hsa_circ_86592,RMVar_hsa_circ_205649,RMVar_hsa_circ_205651,RMVar_hsa_circ_205652,RMVar_hsa_circ_205650,RMVar_hsa_circ_346958,RMVar_hsa_circ_82724,RMVar_hsa_circ_205654,RMVar_hsa_circ_205655,RMVar_hsa_circ_79158,RMVar_hsa_circ_40892,RMVar_hsa_circ_205656,RMVar_hsa_circ_3015,RMVar_hsa_circ_268639 86386 RMVar_ID_86386 Human_SNP_ID_108226181 m1A Human chr2 - 197420534 197420534 197420534 TAAGTGAGACATACCTCTTTTCAGTATGATCCATTTGCTGAGCACAGACCTCCAAAGATTGCAGA TAAGTGAGACATACCTCTTTTCAGTATGATCCGTTTGCTGAGCACAGACCTCCAAAGATTGCAGA T C SF3B1 Ensembl:ENSG00000115524 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:197420485..197421071 32194978 MeRIP-seq:(Medium) rs747647915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57629,Human_RBP_ID_923064,Human_RBP_ID_1906715,Human_RBP_ID_4591118,Human_RBP_ID_8508405,Human_RBP_ID_8844557,Human_RBP_ID_9295342,Human_RBP_ID_13726759,Human_RBP_ID_17947120,Human_RBP_ID_26342198 Human_Splice_Rec_342042,Human_Splice_Rec_342092,Human_Splice_Rec_342140,Human_Splice_Rec_342188,Human_Splice_Rec_342252,Human_Splice_Rec_342264,Human_Splice_Rec_342270,Human_Splice_Rec_342278 Human_miRNA_ID_2881059 RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_205662,RMVar_hsa_circ_205665,RMVar_hsa_circ_116708,RMVar_hsa_circ_329376,RMVar_hsa_circ_377880,RMVar_hsa_circ_277161,RMVar_hsa_circ_109069,RMVar_hsa_circ_205670,RMVar_hsa_circ_205671,RMVar_hsa_circ_205673 86387 RMVar_ID_86387 Human_SNP_ID_108229882 m1A Human chr2 + 197434924 197434924 197434924 AAAAAGGCAGAATCCTAGGAAAAAAGGCTTTTATTAGGCTAGCAACGAAGAAAACACGTAAGCAG AAAAAGGCAGAATCCTAGGAAAAAAGGCTTTTGTTAGGCTAGCAACGAAGAAAACACGTAAGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:197434922..197435025 26863196 MeRIP-seq:(Medium) rs779046825 Functional Loss SNV dbSNP153 33..33 33 - - - 86388 RMVar_ID_86388 Human_SNP_ID_108236505 m1A Human chr2 + 197459872 197459872 197459872 ACAAAGTGGATAATTACTTTATAGTTTCTATAATTTGTGCTTCCTTTTAATTTTTACTGTCACTC ACAAAGTGGATAATTACTTTATAGTTTCTATAGTTTGTGCTTCCTTTTAATTTTTACTGTCACTC A G COQ10B Ensembl:ENSG00000115520 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:197459871..197459964 26863196 MeRIP-seq:(Medium) rs1342301999 Functional Loss SNV dbSNP153 33..33 33 - - - 86389 RMVar_ID_86389 Human_SNP_ID_108244388 m1A Human chr2 - 197488963 197488963 197488963 TTCATTATTATGAATAAGTTTCTTGGGTTCTGAGTCCAAGAATGATTTTGCTTCTGTAGTATTCC TTCATTATTATGAATAAGTTTCTTGGGTTCTGTGTCCAAGAATGATTTTGCTTCTGTAGTATTCC T A HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:197488960..197489302 26863196 MeRIP-seq:(Medium) rs752285480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19102373,Human_RBP_ID_22361190 RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,RMVar_hsa_circ_92396,RMVar_hsa_circ_76261,RMVar_hsa_circ_205682,RMVar_hsa_circ_87075,RMVar_hsa_circ_205684,RMVar_hsa_circ_205685,RMVar_hsa_circ_205686,RMVar_hsa_circ_205683,RMVar_hsa_circ_205681,RMVar_hsa_circ_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_366810,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_205689 86390 RMVar_ID_86390 Human_SNP_ID_108244389 m1A Human chr2 - 197488963 197488963 197488963 TTCATTATTATGAATAAGTTTCTTGGGTTCTGAGTCCAAGAATGATTTTGCTTCTGTAGTATTCC TTCATTATTATGAATAAGTTTCTTGGGTTCTGGGTCCAAGAATGATTTTGCTTCTGTAGTATTCC T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:197488960..197489302 26863196 MeRIP-seq:(Medium) rs752285480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19102373,Human_RBP_ID_22361190 RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,RMVar_hsa_circ_92396,RMVar_hsa_circ_76261,RMVar_hsa_circ_205682,RMVar_hsa_circ_87075,RMVar_hsa_circ_205684,RMVar_hsa_circ_205685,RMVar_hsa_circ_205686,RMVar_hsa_circ_205683,RMVar_hsa_circ_205681,RMVar_hsa_circ_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_366810,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_205689 86391 RMVar_ID_86391 Human_SNP_ID_108246590 m1A Human chr2 + 197497201 197497201 197497201 TTGCTAATCTTCTCGAAGCCTTCCTTGGCTATAGAGCGTGCCAGTACAGTAGCAGTGGTAGTGCC TTGCTAATCTTCTCGAAGCCTTCCTTGGCTATTGAGCGTGCCAGTACAGTAGCAGTGGTAGTGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:197497151..197497275 32194978 MeRIP-seq:(Medium) rs1166759713 Functional Loss SNV dbSNP153 33..33 33 - - - 86392 RMVar_ID_86392 Human_SNP_ID_108246617 m1A Human chr2 - 197497294 197497294 197497294 GCAAAGTCAATTGACTTAAAAGATAAATACAAAAACATTGGAGCTAAACTTGTTCAAGATGTTGC GCAAAGTCAATTGACTTAAAAGATAAATACAAGAACATTGGAGCTAAACTTGTTCAAGATGTTGC T C HSPD1 Ensembl:ENSG00000144381 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8539 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - Human_RBP_ID_59507,Human_RBP_ID_1581866,Human_RBP_ID_1906812,Human_RBP_ID_22246517,Human_RBP_ID_26488131,Human_RBP_ID_27005323,Human_RBP_ID_27285241 Human_Splice_Rec_342306,Human_Splice_Rec_342326,Human_Splice_Rec_342354,Human_Splice_Rec_342368,Human_Splice_Rec_342376,Human_Splice_Rec_342384,Human_Splice_Rec_342390,Human_Splice_Rec_342394,Human_Splice_Rec_342400,Human_Splice_Rec_342406 Clinvar_Rec_464 GWAS_ID_10597,GWAS_ID_10598,GWAS_ID_10599,GWAS_ID_10600,GWAS_ID_10601,GWAS_ID_10602 RMVar_hsa_circ_115375,RMVar_hsa_circ_87075,RMVar_hsa_circ_205685,RMVar_hsa_circ_205686,RMVar_hsa_circ_126781,RMVar_hsa_circ_57034,RMVar_hsa_circ_205687,RMVar_hsa_circ_122492,RMVar_hsa_circ_205691,RMVar_hsa_circ_332331,RMVar_hsa_circ_205695,RMVar_hsa_circ_94462,RMVar_hsa_circ_281585,RMVar_hsa_circ_205698,RMVar_hsa_circ_345564 86393 RMVar_ID_86393 Human_SNP_ID_108247384 m1A Human chr2 - 197499741 197499741 197499741 CCTTCCCGCACCACCTCCCCCCGGCTCCTGCGACCCCCGAGTGGGCCTTCCTCCTCTGCGGTCCA CCTTCCCGCACCACCTCCCCCCGGCTCCTGCGGCCCCCGAGTGGGCCTTCCTCCTCTGCGGTCCA T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:197499737..197499900;chr2:197499734..197499951;chr2:197499736..197499925 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1201156016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19102383 RMVar_hsa_circ_115375,RMVar_hsa_circ_205686 86394 RMVar_ID_86394 Human_SNP_ID_108247648 m1A Human chr2 - 197500291 197500291 197500291 CAGCGGTCGCCGCTAGCCCCCTCGCCCCTCCCAGGGAGGGAGGGCGGTCGCCCCGACGCGCACCG CAGCGGTCGCCGCTAGCCCCCTCGCCCCTCCCCGGGAGGGAGGGCGGTCGCCCCGACGCGCACCG T G HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:197500191..197500290 26863410 MeRIP-seq:(Medium) rs996257279 Functional Loss SNV dbSNP153 33..33 33 - - - 86395 RMVar_ID_86395 Human_SNP_ID_108247695 m1A Human chr2 + 197500376 197500376 197500376 TGGGTGATTTTTTCACGTGTCGCCAGGGCCGGACTGCGAGTCTCTTTGCGGCGCTACACTAGAGC TGGGTGATTTTTTCACGTGTCGCCAGGGCCGGGCTGCGAGTCTCTTTGCGGCGCTACACTAGAGC A G HSPE1 Ensembl:ENSG00000115541 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:197500240..197500389 32194978 MeRIP-seq:(Medium) rs750052223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541456,Human_RBP_ID_776828,Human_RBP_ID_1021387,Human_RBP_ID_4591208,Human_RBP_ID_6869274,Human_RBP_ID_9330768,Human_RBP_ID_13727857,Human_RBP_ID_18442899,Human_RBP_ID_22246539,Human_RBP_ID_22450051,Human_RBP_ID_22504908,Human_RBP_ID_23845936,Human_RBP_ID_27005332 Human_Splice_Rec_342411,Human_Splice_Rec_342415,Human_Splice_Rec_342417,Human_Splice_Rec_342421,Human_Splice_Rec_342435 86396 RMVar_ID_86396 Human_SNP_ID_108247696 m1A Human chr2 + 197500376 197500376 197500376 TGGGTGATTTTTTCACGTGTCGCCAGGGCCGGACTGCGAGTCTCTTTGCGGCGCTACACTAGAGC TGGGTGATTTTTTCACGTGTCGCCAGGGCCGGTCTGCGAGTCTCTTTGCGGCGCTACACTAGAGC A T HSPE1 Ensembl:ENSG00000115541 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:197500240..197500389 32194978 MeRIP-seq:(Medium) rs750052223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541456,Human_RBP_ID_776828,Human_RBP_ID_1021387,Human_RBP_ID_4591208,Human_RBP_ID_6869274,Human_RBP_ID_9330768,Human_RBP_ID_13727857,Human_RBP_ID_18442899,Human_RBP_ID_22246539,Human_RBP_ID_22450051,Human_RBP_ID_22504908,Human_RBP_ID_23845936,Human_RBP_ID_27005332 Human_Splice_Rec_342411,Human_Splice_Rec_342415,Human_Splice_Rec_342417,Human_Splice_Rec_342421,Human_Splice_Rec_342435 86397 RMVar_ID_86397 Human_SNP_ID_108247740 m1A Human chr2 + 197500436 197500436 197500436 AGAGCAGAGTACGAGTCTGAGGCGGAGGGAGTAATGGTGAGTCCCGCGTGGCCCCGAGGCCTGCA AGAGCAGAGTACGAGTCTGAGGCGGAGGGAGTCATGGTGAGTCCCGCGTGGCCCCGAGGCCTGCA A C HSPE1-MOB4,HSPE1 Ensembl:ENSG00000270757,Ensembl:ENSG00000115541 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:197500175..197500488 26863196 MeRIP-seq:(Medium) rs1237138724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776828,Human_RBP_ID_1134326,Human_RBP_ID_4623784,Human_RBP_ID_5422658,Human_RBP_ID_9330768,Human_RBP_ID_13727863,Human_RBP_ID_19098529,Human_RBP_ID_22452575,Human_RBP_ID_23845938 Human_Splice_Rec_342411,Human_Splice_Rec_342415,Human_Splice_Rec_342417,Human_Splice_Rec_342421,Human_Splice_Rec_342435 86398 RMVar_ID_86398 Human_SNP_ID_108247950 m1A Human chr2 + 197501054 197501054 197501054 TGATAATGTGATTACATTTAGTTTTTGTTTCAAAACATTTCTCTTCCTACAGGCAGGACAAGCGT TGATAATGTGATTACATTTAGTTTTTGTTTCAGAACATTTCTCTTCCTACAGGCAGGACAAGCGT A G HSPE1-MOB4,HSPE1 Ensembl:ENSG00000270757,Ensembl:ENSG00000115541 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:197501051..197501150 26863196 MeRIP-seq:(Medium) rs755791347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1240773,Human_RBP_ID_25496847 86399 RMVar_ID_86399 Human_SNP_ID_108247982 m1A Human chr2 - 197501124 197501124 197501124 CCTTTGGTTACAGTTTCAGCAGCACTCCTTTCAACCAATACTCGGTCAAAGAGTGGAAGAAACTT CCTTTGGTTACAGTTTCAGCAGCACTCCTTTCCACCAATACTCGGTCAAAGAGTGGAAGAAACTT T G HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:197501051..197501150 26863196 MeRIP-seq:(Medium) rs372780408 Functional Loss SNV dbSNP153 33..33 33 - - - 86400 RMVar_ID_86400 Human_SNP_ID_108247997 m1A Human chr2 + 197501174 197501173 197501174 AACTGTAACCAAAGGAGGCATTATGCTTCCAGAAAAATCTCAAGGAAAAGTATTGCAAGCAACAG AACTGTAACCAAAGGAGGCATTATGCTTCCAG_AAAATCTCAAGGAAAAGTATTGCAAGCAACAG GA G HSPE1-MOB4,HSPE1 Ensembl:ENSG00000270757,Ensembl:ENSG00000115541 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:197501051..197501200 26863410 MeRIP-seq:(Medium) rs778457721 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_342419,Human_Splice_Rec_342423,Human_Splice_Rec_342433,Human_Splice_Rec_342437 86401 RMVar_ID_86401 Human_SNP_ID_108300241 m1A Human chr2 - 197705462 197705462 197705462 CTGTAGTAGCGTGGGCCGAAGTCCTCCAGGAGAGACAGCCTACTAGCCCCCGTGCGTCCTAGCAG CTGTAGTAGCGTGGGCCGAAGTCCTCCAGGAGGGACAGCCTACTAGCCCCCGTGCGTCCTAGCAG T C lnc-BOLL-1 RNACentral:URS0000D5D518 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:197705415..197705509 26863196 MeRIP-seq:(Medium) rs1364336331 Functional Loss SNV dbSNP153 33..33 33 - - - 86402 RMVar_ID_86402 Human_SNP_ID_108323200 m1A Human chr2 - 197804885 197804885 197804885 CGGGCAGAGACGTCCTCGGGCTTCGGTCTAGGAGGCTAGCAGTCCGGCGGGGGACGGTGGCGGGA CGGGCAGAGACGTCCTCGGGCTTCGGTCTAGGTGGCTAGCAGTCCGGCGGGGGACGGTGGCGGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:197804665..197804962 26863196 MeRIP-seq:(Medium) rs1217839839 Functional Loss SNV dbSNP153 33..33 33 - - - 86403 RMVar_ID_86403 Human_SNP_ID_108717419 m1A Human chr2 - 199458348 199458348 199458348 CTCCCCTTCCTCTTCCCTCCTCCCTGCCTCCCACCCGCCCCTCGCCTGTCCCTCTGCCTCCTTCG CTCCCCTTCCTCTTCCCTCCTCCCTGCCTCCCCCCCGCCCCTCGCCTGTCCCTCTGCCTCCTTCG T G SATB2 Ensembl:ENSG00000119042 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:199458165..199458564 26863196 MeRIP-seq:(Medium) rs958587661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638954,Human_RBP_ID_5131929,Human_RBP_ID_5444376,Human_RBP_ID_9330774,Human_RBP_ID_9429407,Human_RBP_ID_17085081,Human_RBP_ID_17392850,Human_RBP_ID_17569360,Human_RBP_ID_18948455,Human_RBP_ID_22721563,Human_RBP_ID_26787300,Human_RBP_ID_27476668 RMVar_hsa_circ_23032,RMVar_hsa_circ_47173 86404 RMVar_ID_86404 Human_SNP_ID_108717614 m1A Human chr2 + 199458729 199458729 199458729 CTGTTAACTGCGCGGAGTACTTTCGACTTTGGAGATAGGAGGGCGATCGCCTCCCCCACCCACCG CTGTTAACTGCGCGGAGTACTTTCGACTTTGGGGATAGGAGGGCGATCGCCTCCCCCACCCACCG A G SATB2-AS1 Ensembl:ENSG00000225953 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs114693875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17947414 GWAS_ID_10603,GWAS_ID_10604,GWAS_ID_10605 86405 RMVar_ID_86405 Human_SNP_ID_108717615 m1A Human chr2 + 199458729 199458729 199458729 CTGTTAACTGCGCGGAGTACTTTCGACTTTGGAGATAGGAGGGCGATCGCCTCCCCCACCCACCG CTGTTAACTGCGCGGAGTACTTTCGACTTTGGTGATAGGAGGGCGATCGCCTCCCCCACCCACCG A T SATB2-AS1 Ensembl:ENSG00000225953 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs114693875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17947414 GWAS_ID_10603,GWAS_ID_10604,GWAS_ID_10605 86406 RMVar_ID_86406 Human_SNP_ID_108717714 m1A Human chr2 - 199458907 199458907 199458907 CCCGACTATTGTTCCGGACTCGCGGCCGTGCCAGCTTTGAAGGAGAAGCGGCCTTCCCTGCGCGC CCCGACTATTGTTCCGGACTCGCGGCCGTGCCGGCTTTGAAGGAGAAGCGGCCTTCCCTGCGCGC T C SATB2 Ensembl:ENSG00000119042 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:199458859..199459051 26863196 MeRIP-seq:(Medium) rs539694739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541656 RMVar_hsa_circ_23032,RMVar_hsa_circ_47173 86407 RMVar_ID_86407 Human_SNP_ID_108717936 m1A Human chr2 + 199459596 199459581 199459596 TGAGGCCAGAGAATCCCCCCTCAACTGGTTGCACCTCATGTCCCTCCCGCACACGTTGACTCTCC TGAGGCCAGAGAATCCCC_______________CCTCATGTCCCTCCCGCACACGTTGACTCTCC CCCTCAACTGGTTGCA C SATB2-AS1 Ensembl:ENSG00000225953 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:199459546..199459649 26863196 MeRIP-seq:(Medium) rs1559069150 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_5652169,Human_RBP_ID_27476670 86408 RMVar_ID_86408 Human_SNP_ID_108821697 m1A Human chr2 - 199911396 199911396 199911396 CGCGAGAGCGGTTCGGAGGTGGAGGGTGGCGGAGGGGTTCCTGAGGGAGGGACTTCAGCAGGCGG CGCGAGAGCGGTTCGGAGGTGGAGGGTGGCGGGGGGGTTCCTGAGGGAGGGACTTCAGCAGGCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:199911333..199911422 26863196 MeRIP-seq:(Medium) rs557139782 Functional Loss SNV dbSNP153 33..33 33 - - - 86409 RMVar_ID_86409 Human_SNP_ID_108832790 m1A Human chr2 - 199955695 199955695 199955695 GTGTCGGAGAAAGAGACTGGAGAGCAAAGTGGACCTGTTGCTGCAGCCTCTGGTGAGTCGGCCCC GTGTCGGAGAAAGAGACTGGAGAGCAAAGTGGCCCTGTTGCTGCAGCCTCTGGTGAGTCGGCCCC T G TYW5 Ensembl:ENSG00000162971 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:199955634..199955735 26863410 MeRIP-seq:(Medium) rs1429619923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5470329 86410 RMVar_ID_86410 Human_SNP_ID_108832876 m1A Human chr2 - 199955879 199955877 199955880 GTGGCCGACGGCAGCCTCACCTCGGCCACAGCAGGAGTCCGGAGTCGGACGGCCCCGCAGGGCAG GTGGCCGACGGCAGCCTCACCTCGGCCACAG___GAGTCCGGAGTCGGACGGCCCCGCAGGGCAG CCTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:199955830..199955952 26863196 MeRIP-seq:(Medium) rs755372527 Functional Loss DEL dbSNP153 32..34 33 - - - 86411 RMVar_ID_86411 Human_SNP_ID_108912003 m1A Human chr2 + 200306750 200306750 200306750 CCGGGGGCCGAGCTGGCTGCGCCCTCCGCTGCAAGCGCCGGCAGCGCGGGGCGAGCTCCGGACGG CCGGGGGCCGAGCTGGCTGCGCCCTCCGCTGCCAGCGCCGGCAGCGCGGGGCGAGCTCCGGACGG A C SPATS2L Ensembl:ENSG00000196141 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:200306460..200306878;chr2:200306580..200306925;chr2:200306388..200306938 26863196 MeRIP-seq:(Medium) rs1263763569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622813,Human_RBP_ID_5381869,Human_RBP_ID_8728564,Human_RBP_ID_18421982,Human_RBP_ID_22721567,Human_RBP_ID_23212164,Human_RBP_ID_23257936 86412 RMVar_ID_86412 Human_SNP_ID_108944081 m1A Human chr2 + 200453084 200453084 200453084 TCAGGGTTAAATAAGAGTCAGTGGAAGTGGAGAGGTGCATGGGACAGACAGACATTTCTGGGGTA TCAGGGTTAAATAAGAGTCAGTGGAAGTGGAGGGGTGCATGGGACAGACAGACATTTCTGGGGTA A G SPATS2L Ensembl:ENSG00000196141 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:200453078..200453243 26863196 MeRIP-seq:(Medium) rs1358601877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59766,RMVar_hsa_circ_358282,RMVar_hsa_circ_107541,RMVar_hsa_circ_6883,RMVar_hsa_circ_205787,RMVar_hsa_circ_205791,RMVar_hsa_circ_331561,RMVar_hsa_circ_41486 86413 RMVar_ID_86413 Human_SNP_ID_108948479 m1A Human chr2 + 200472952 200472952 200472952 ACAGAGTAACTTTTCCCGAAAATCATCCACTCACAATAAGCCCTCTGAAGGCAAAGCGGCAAACC ACAGAGTAACTTTTCCCGAAAATCATCCACTCTCAATAAGCCCTCTGAAGGCAAAGCGGCAAACC A T SPATS2L Ensembl:ENSG00000196141 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:200472902..200473087 26863196 MeRIP-seq:(Medium) rs1228688147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8106443,Human_RBP_ID_9385292,Human_RBP_ID_17280028,Human_RBP_ID_21931119 Human_Splice_Rec_343757 RMVar_hsa_circ_107541,RMVar_hsa_circ_205787,RMVar_hsa_circ_32393 86414 RMVar_ID_86414 Human_SNP_ID_108962588 m1A Human chr2 + 200532936 200532936 200532936 AAAATGTATTTATCAGTTATACTTTTTCTTTTATTAATCAATACTATGATTTTTTTTTCTTTCAC AAAATGTATTTATCAGTTATACTTTTTCTTTTGTTAATCAATACTATGATTTTTTTTTCTTTCAC A G SGO2 Ensembl:ENSG00000163535 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:200532934..200533029 26863196 MeRIP-seq:(Medium) rs769365187 Functional Loss SNV dbSNP153 33..33 33 - - - 86415 RMVar_ID_86415 Human_SNP_ID_109027509 m1A Human chr2 + 200811639 200811639 200811639 CGAGACCGGCGGGGGCCGGCTCCGCTCTTCCAACCCCTCCATGTGTGAAGAGGGCGGACGACGCA CGAGACCGGCGGGGGCCGGCTCCGCTCTTCCAGCCCCTCCATGTGTGAAGAGGGCGGACGACGCA A G BZW1 Ensembl:ENSG00000082153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:200811591..200811741 26863196 MeRIP-seq:(Medium) rs1384259903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541834,Human_RBP_ID_1021487,Human_RBP_ID_4629279,Human_RBP_ID_9385294 Human_Splice_Rec_344257 86416 RMVar_ID_86416 Human_SNP_ID_109027519 m1A Human chr2 + 200811657 200811657 200811657 GCTCCGCTCTTCCAACCCCTCCATGTGTGAAGAGGGCGGACGACGCAGCGGGGGAAGAAAAATAA GCTCCGCTCTTCCAACCCCTCCATGTGTGAAGGGGGCGGACGACGCAGCGGGGGAAGAAAAATAA A G BZW1 Ensembl:ENSG00000082153 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:200811612..200811826 26863196 MeRIP-seq:(Medium) rs930947094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541834,Human_RBP_ID_4591804,Human_RBP_ID_6872000,Human_RBP_ID_9385294 Human_Splice_Rec_344257 86417 RMVar_ID_86417 Human_SNP_ID_109041247 m1A Human chr2 - 200859682 200859682 200859682 TTTGGAAAAGTTGTGGAGTGCATCGATCATAAAGCGTAAGTTTCCCATGTTGGGATTACTTTTAG TTTGGAAAAGTTGTGGAGTGCATCGATCATAACGCGTAAGTTTCCCATGTTGGGATTACTTTTAG T G CLK1 Ensembl:ENSG00000013441 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:200859676..200859700 26863196 MeRIP-seq:(Medium) rs754931982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919089,Human_RBP_ID_5146933,Human_RBP_ID_9100717,Human_RBP_ID_9347793,Human_RBP_ID_19002797,Human_RBP_ID_19098552,Human_RBP_ID_22599362,Human_RBP_ID_22668083,Human_RBP_ID_22743369,Human_RBP_ID_22814431,Human_RBP_ID_22996905,Human_RBP_ID_24546552,Human_RBP_ID_25498501,Human_RBP_ID_27691031 Human_Splice_Rec_344384,Human_Splice_Rec_344385,Human_Splice_Rec_344405,Human_Splice_Rec_344421,Human_Splice_Rec_344442,Human_Splice_Rec_344443,Human_Splice_Rec_344463,Human_Splice_Rec_344502,Human_Splice_Rec_344503,Human_Splice_Rec_344524,Human_Splice_Rec_344525 RMVar_hsa_circ_984,RMVar_hsa_circ_31004,RMVar_hsa_circ_1814,RMVar_hsa_circ_101138,RMVar_hsa_circ_274777,RMVar_hsa_circ_205819,RMVar_hsa_circ_205820,RMVar_hsa_circ_16527,RMVar_hsa_circ_49580,RMVar_hsa_circ_300277,RMVar_hsa_circ_205824,RMVar_hsa_circ_9441,RMVar_hsa_circ_291252,RMVar_hsa_circ_26549,RMVar_hsa_circ_205825,RMVar_hsa_circ_205826,RMVar_hsa_circ_344099 86418 RMVar_ID_86418 Human_SNP_ID_109042062 m1A Human chr2 - 200862378 200862378 200862378 CCTTCCTAAGGGTGGGGGAGATTACAAAGTATATTGATCAGTTAGGTTGGGGCAGAAATAAATCA CCTTCCTAAGGGTGGGGGAGATTACAAAGTATGTTGATCAGTTAGGTTGGGGCAGAAATAAATCA T C CLK1 Ensembl:ENSG00000013441 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:200862341..200862639 26863196 MeRIP-seq:(Medium) rs921643427 Functional Loss SNV dbSNP153 33..33 33 - - - 86419 RMVar_ID_86419 Human_SNP_ID_109042655 m1A Human chr2 + 200864193 200864193 200864193 CCCCCTCAACGGGGAGCCTCGCCTTTCCGGCCACAGGGCCGAAGCCGGCCTCCGCCCAGCCGCCA CCCCCTCAACGGGGAGCCTCGCCTTTCCGGCCGCAGGGCCGAAGCCGGCCTCCGCCCAGCCGCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:200864159..200864293 26863196 MeRIP-seq:(Medium) rs747479913 Functional Loss SNV dbSNP153 33..33 33 - - - 86420 RMVar_ID_86420 Human_SNP_ID_109042656 m1A Human chr2 + 200864193 200864193 200864193 CCCCCTCAACGGGGAGCCTCGCCTTTCCGGCCACAGGGCCGAAGCCGGCCTCCGCCCAGCCGCCA CCCCCTCAACGGGGAGCCTCGCCTTTCCGGCCTCAGGGCCGAAGCCGGCCTCCGCCCAGCCGCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:200864159..200864293 26863196 MeRIP-seq:(Medium) rs747479913 Functional Loss SNV dbSNP153 33..33 33 - - - 86421 RMVar_ID_86421 Human_SNP_ID_109044675 m1A Human chr2 - 200871389 200871389 200871389 ATTCATGCCAACCCATTTGCTCAGTAGCTATGATAGACCTGGACAAATAACTTGACAAATTGCTG ATTCATGCCAACCCATTTGCTCAGTAGCTATGGTAGACCTGGACAAATAACTTGACAAATTGCTG T C PPIL3 Ensembl:ENSG00000240344 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11892119 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_13735638,Human_RBP_ID_17278106,Human_RBP_ID_18752510,Human_RBP_ID_26661894 Human_miRNA_ID_1136263,Human_miRNA_ID_1138776 GWAS_ID_10606,GWAS_ID_10607,GWAS_ID_10608,GWAS_ID_10609,GWAS_ID_10610 86422 RMVar_ID_86422 Human_SNP_ID_109054179 m1A Human chr2 - 200909521 200909521 200909521 TTTTGAATTTTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCT TTTTGAATTTTTAGCAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAATTCCTGACCT T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1322159844 Functional Loss SNV dbSNP153 33..33 33 - - - 86423 RMVar_ID_86423 Human_SNP_ID_109066380 m1A Human chr2 - 200963571 200963571 200963571 GGAAATTGGCTTTTCCCGTTGGGGCCGAAGGTACCTTCCCTGCGGCGGCGACTCAGCGGGGTGTC GGAAATTGGCTTTTCCCGTTGGGGCCGAAGGTTCCTTCCCTGCGGCGGCGACTCAGCGGGGTGTC T A ORC2 Ensembl:ENSG00000115942 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:200963490..200963626 26863196 MeRIP-seq:(Medium) rs907892452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_541937,Human_RBP_ID_4591994,Human_RBP_ID_5470335,Human_RBP_ID_9331255,Human_RBP_ID_22077382,Human_RBP_ID_22504950 Human_Splice_Rec_344779,Human_Splice_Rec_344835 RMVar_hsa_circ_88925,RMVar_hsa_circ_205838 86424 RMVar_ID_86424 Human_SNP_ID_109091524 m1A Human chr2 - 201071569 201071569 201071569 CGGTGCTGTCTTTGGGGGAGGCAAAGTGCTAGATGAAGAGGGGTTTTCTTCTCCTTCGGCCGCGG CGGTGCTGTCTTTGGGGGAGGCAAAGTGCTAGTTGAAGAGGGGTTTTCTTCTCCTTCGGCCGCGG T A FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:201071154..201071639 26863196 MeRIP-seq:(Medium) rs905083353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777770,Human_RBP_ID_18421991,Human_RBP_ID_25499389 Human_Splice_Rec_344959 86425 RMVar_ID_86425 Human_SNP_ID_109091525 m1A Human chr2 - 201071569 201071569 201071569 CGGTGCTGTCTTTGGGGGAGGCAAAGTGCTAGATGAAGAGGGGTTTTCTTCTCCTTCGGCCGCGG CGGTGCTGTCTTTGGGGGAGGCAAAGTGCTAGGTGAAGAGGGGTTTTCTTCTCCTTCGGCCGCGG T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:201071154..201071639 26863196 MeRIP-seq:(Medium) rs905083353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777770,Human_RBP_ID_18421991,Human_RBP_ID_25499389 Human_Splice_Rec_344959 86426 RMVar_ID_86426 Human_SNP_ID_109094891 m1A Human chr2 - 201085507 201085507 201085507 CCCCATTTGAATCCTTTAAAGAATACATCAGAAAAGGAAACACTCTTTGCAAAGCCACCCATGTA CCCCATTTGAATCCTTTAAAGAATACATCAGACAAGGAAACACTCTTTGCAAAGCCACCCATGTA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:201078930..201085558 32194978 MeRIP-seq:(Medium) rs1366301117 Functional Loss SNV dbSNP153 33..33 33 - - - 86427 RMVar_ID_86427 Human_SNP_ID_109104078 m1A Human chr2 + 201124713 201124712 201124714 TTGGAGAGGGTGAGGTCTAAAGCAGGGGGAACAGAATGGCTAGGGGAATGAGTTTGGATGAGAGA TTGGAGAGGGTGAGGTCTAAAGCAGGGGGAAC__AATGGCTAGGGGAATGAGTTTGGATGAGAGA CAG C CFLAR Ensembl:ENSG00000003402 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:201124677..201125002 26863196 MeRIP-seq:(Medium) rs1476702810 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_205876,RMVar_hsa_circ_116078 86428 RMVar_ID_86428 Human_SNP_ID_109104192 m1A Human chr2 + 201125439 201125438 201125440 GCTTTATTTTTTAAGATGGAAGAGACTTGCACATGTTTACAAGCTGGGAGGAGCCGTCTCTGGAG GCTTTATTTTTTAAGATGGAAGAGACTTGCAC__GTTTACAAGCTGGGAGGAGCCGTCTCTGGAG CAT C CFLAR Ensembl:ENSG00000003402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:201125434..201125678 26863196 MeRIP-seq:(Medium) rs1056343653 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_205876,RMVar_hsa_circ_116078 86429 RMVar_ID_86429 Human_SNP_ID_109131286 m1A Human chr2 - 201238099 201238099 201238099 CTTGGAATACTCTTCCTCTTTGATATCTCCAAAGTGTGAATCCACACAACACTGTCCACTTCCTC CTTGGAATACTCTTCCTCTTTGATATCTCCAAGGTGTGAATCCACACAACACTGTCCACTTCCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:201238085..201238169 26863196 MeRIP-seq:(Medium) rs1370838821 Functional Loss SNV dbSNP153 33..33 33 - - - 86430 RMVar_ID_86430 Human_SNP_ID_109164116 m1A Human chr2 - 201380021 201380021 201380021 GTTTCCCCTGTTAATATCTGGTTAAATTATGTATCCATCAAATGGTATGCTCGCAGCATTAGCAA GTTTCCCCTGTTAATATCTGGTTAAATTATGTTTCCATCAAATGGTATGCTCGCAGCATTAGCAA T A TRAK2 Ensembl:ENSG00000115993 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:201379970..201380053 32194978 MeRIP-seq:(Medium) rs889293952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94151,RMVar_hsa_circ_115027,RMVar_hsa_circ_124257,RMVar_hsa_circ_205894,RMVar_hsa_circ_205895,RMVar_hsa_circ_205896 86431 RMVar_ID_86431 Human_SNP_ID_109164187 m1A Human chr2 + 201380405 201380405 201380405 CCTCCATTAGGGCTCATCCCAATTTTATTTCCATTCCTCCATTCCCCCTTTCACATTCACAACCC CCTCCATTAGGGCTCATCCCAATTTTATTTCCGTTCCTCCATTCCCCCTTTCACATTCACAACCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:201380354..201380451 26863196 MeRIP-seq:(Medium) rs1361096289 Functional Loss SNV dbSNP153 33..33 33 - - - 86432 RMVar_ID_86432 Human_SNP_ID_109180185 m1A Human chr2 - 201451873 201451873 201451873 GGCTGCCAGCGGTGCGGACAGGGGCGGGCGCCAGAGCCCTGCTCGCGGAGGGGCGAGGCGAGCGC GGCTGCCAGCGGTGCGGACAGGGGCGGGCGCCGGAGCCCTGCTCGCGGAGGGGCGAGGCGAGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:201451826..201452048 26863196 MeRIP-seq:(Medium) rs1275919630 Functional Loss SNV dbSNP153 33..33 33 - - - 86433 RMVar_ID_86433 Human_SNP_ID_109223701 m1A Human chr2 - 201642644 201642644 201642644 GGCGCCAGGTGCTTGGGGGCCGGCGGCCGCCGAGGCCGGCTAAACGCAGAATGGGGAAGAATCCT GGCGCCAGGTGCTTGGGGGCCGGCGGCCGCCGCGGCCGGCTAAACGCAGAATGGGGAAGAATCCT T G TMEM237 Ensembl:ENSG00000155755 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:201642556..201642665 26863196 MeRIP-seq:(Medium) rs1313979635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243082,Human_RBP_ID_920622,Human_RBP_ID_4624962,Human_RBP_ID_18421995 Human_Splice_Rec_346165,Human_Splice_Rec_346215,Human_Splice_Rec_346325 RMVar_hsa_circ_126400,RMVar_hsa_circ_205924 86434 RMVar_ID_86434 Human_SNP_ID_109254183 m1A Human chr2 + 201768911 201768911 201768911 AGTCCATCGGTCAGTGGGAACACTCCATCACCAAATCATTCCTTCTTTACAGAAAGTCTATCAAG AGTCCATCGGTCAGTGGGAACACTCCATCACCCAATCATTCCTTCTTTACAGAAAGTCTATCAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:201768827..201768911 26863196 MeRIP-seq:(Medium) rs758284102 Functional Loss SNV dbSNP153 33..33 33 - - - 86435 RMVar_ID_86435 Human_SNP_ID_109316929 m1A Human chr2 + 202034495 202034495 202034495 CGGCGCCTTCGCGGCGCGGGCACCCAGGCGGCAGCGCCCTTTGCTCCACGCCGCCCACGGCCCGG CGGCGCCTTCGCGGCGCGGGCACCCAGGCGGCCGCGCCCTTTGCTCCACGCCGCCCACGGCCCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:202034449..202034604 26863196 MeRIP-seq:(Medium) rs1046802213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542196 86436 RMVar_ID_86436 Human_SNP_ID_109365137 m1A Human chr2 + 202238430 202238430 202238430 AAGGCCCTGGCCACCGCCGTTGGATGGCTCCCAGCCCGGTACCTGGTCAGACATGATGACGGTGG AAGGCCCTGGCCACCGCCGTTGGATGGCTCCCGGCCCGGTACCTGGTCAGACATGATGACGGTGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:202238426..202238575 26863410 MeRIP-seq:(Medium) rs1342528057 Functional Loss SNV dbSNP153 33..33 33 - - - 86437 RMVar_ID_86437 Human_SNP_ID_109365179 m1A Human chr2 + 202238502 202238502 202238502 CGGGGGTCTCCGCACAGCAGCGGCCTCGGGTAAGCAGAACCTCGCTCCGGGGTTTACAAATCCTT CGGGGGTCTCCGCACAGCAGCGGCCTCGGGTAGGCAGAACCTCGCTCCGGGGTTTACAAATCCTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:202238451..202238550 32194978 MeRIP-seq:(Medium) rs1434272849 Functional Loss SNV dbSNP153 33..33 33 - - - 86438 RMVar_ID_86438 Human_SNP_ID_109365193 m1A Human chr2 - 202238522 202238522 202238522 TTGTGCTGTGGGGAAGGGAGAAGGATTTGTAAACCCCGGAGCGAGGTTCTGCTTACCCGAGGCCG TTGTGCTGTGGGGAAGGGAGAAGGATTTGTAACCCCCGGAGCGAGGTTCTGCTTACCCGAGGCCG T G SUMO1 Ensembl:ENSG00000116030 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202238442..202238600 26863196 MeRIP-seq:(Medium) rs1201987742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_146155,Human_RBP_ID_542256,Human_RBP_ID_1582277,Human_RBP_ID_3611118,Human_RBP_ID_4592585,Human_RBP_ID_5528775,Human_RBP_ID_8942714,Human_RBP_ID_9100902,Human_RBP_ID_13740695,Human_RBP_ID_17392851,Human_RBP_ID_18421996,Human_RBP_ID_22077818,Human_RBP_ID_22451690,Human_RBP_ID_27005832 Human_Splice_Rec_347235,Human_Splice_Rec_347243,Human_Splice_Rec_347251,Human_Splice_Rec_347261,Human_Splice_Rec_347267,Human_Splice_Rec_347273,Human_Splice_Rec_347289,Human_Splice_Rec_347297 RMVar_hsa_circ_50418 86439 RMVar_ID_86439 Human_SNP_ID_109365195 m1A Human chr2 + 202238529 202238529 202238529 GGGTAAGCAGAACCTCGCTCCGGGGTTTACAAATCCTTCTCCCTTCCCCACAGCACAACACCGCG GGGTAAGCAGAACCTCGCTCCGGGGTTTACAACTCCTTCTCCCTTCCCCACAGCACAACACCGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:202238426..202238575 26863196 MeRIP-seq:(Medium) rs1044107271 Functional Loss SNV dbSNP153 33..33 33 - - - 86440 RMVar_ID_86440 Human_SNP_ID_109372524 m1A Human chr2 + 202265998 202265998 202265998 GTGGGTTACGCCATCTTTAAGGTAGGTGGGAGAGCGAGCCGTTAAAGGGGGAAGGCGGATGCTGG GTGGGTTACGCCATCTTTAAGGTAGGTGGGAGGGCGAGCCGTTAAAGGGGGAAGGCGGATGCTGG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:202265992..202266092 26863196 MeRIP-seq:(Medium) rs777314567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5381897,Human_RBP_ID_19098583,Human_RBP_ID_26787327 RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 86441 RMVar_ID_86441 Human_SNP_ID_109383099 m1A Human chr2 - 202303380 202303376 202303380 TTTCTTTTTCTTCTTTTTCTCTGGACTCTGAAAATAGCCAACAAGAATGCTTTGAAAGAGCTGAA TTTCTTTTTCTTCTTTTTCTCTGGACTCTGAA____GCCAACAAGAATGCTTTGAAAGAGCTGAA CTATT C AC064836.3 Ensembl:ENSG00000286223 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202303376..202303475 26863196 MeRIP-seq:(Medium) rs781280871 Functional Loss DEL dbSNP153 33..36 33 - - - Human_Splice_Rec_347415 86442 RMVar_ID_86442 Human_SNP_ID_109383100 m1A Human chr2 + 202303378 202303378 202303378 ATTTCAGCTCTTTCAAAGCATTCTTGTTGGCTATTTTCAGAGTCCAGAGAAAAAGAAGAAAAAGA ATTTCAGCTCTTTCAAAGCATTCTTGTTGGCTGTTTTCAGAGTCCAGAGAAAAAGAAGAAAAAGA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:202303376..202303425 26863196 MeRIP-seq:(Medium) rs1559269139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919124,Human_RBP_ID_2614974,Human_RBP_ID_4592688,Human_RBP_ID_25584567 RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_125140,RMVar_hsa_circ_205965,RMVar_hsa_circ_102304,RMVar_hsa_circ_205972,RMVar_hsa_circ_205973,RMVar_hsa_circ_84719,RMVar_hsa_circ_205974 86443 RMVar_ID_86443 Human_SNP_ID_109401732 m1A Human chr2 - 202376427 202376427 202376427 GGGCGGGGGGCGGCGGGAGGGCGGATGAAGGTAGCCGGGGAAGGGGGTGGGCAGGGAGGCGGCGA GGGCGGGGGGCGGCGGGAGGGCGGATGAAGGTGGCCGGGGAAGGGGGTGGGCAGGGAGGCGGCGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:202376419..202376553 26863196 MeRIP-seq:(Medium) rs1340707846 Functional Loss SNV dbSNP153 33..33 33 - - - 86444 RMVar_ID_86444 Human_SNP_ID_109401784 m1A Human chr2 + 202376554 202376530 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCG________________________GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCGGCGGCGGCGGCGGCAGCAGCA G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs1196119221 Functional Loss DEL dbSNP153 10..33 33 - - - Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86445 RMVar_ID_86445 Human_SNP_ID_109401789 m1A Human chr2 + 202376554 202376536 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCG__________________GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCGGCGGCGGCAGCAGCA G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs1196827773 Functional Loss DEL dbSNP153 16..33 33 - - - Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86446 RMVar_ID_86446 Human_SNP_ID_109401796 m1A Human chr2 + 202376554 202376542 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCG____________GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCGGCAGCAGCA G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs1368674990 Functional Loss DEL dbSNP153 22..33 33 - - - Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86447 RMVar_ID_86447 Human_SNP_ID_109401803 m1A Human chr2 + 202376554 202376545 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCGGCG_________GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCAGCAGCA G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs568136148 Functional Loss DEL dbSNP153 25..33 33 - - - Human_miRNA_ID_3003275 Clinvar_Rec_465 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86448 RMVar_ID_86448 Human_SNP_ID_109401804 m1A Human chr2 + 202376554 202376545 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCGGCGGCA______GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCAGCAGCA GGCA BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs568136148 Functional Loss DEL dbSNP153 28..33 33 - - - Human_miRNA_ID_3003275 Clinvar_Rec_465 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86449 RMVar_ID_86449 Human_SNP_ID_109401805 m1A Human chr2 + 202376554 202376545 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCGGCGGCAGCA___GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GGCAGCAGCA GGCAGCA BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs568136148 Functional Loss DEL dbSNP153 31..33 33 - - - Human_miRNA_ID_3003275 Clinvar_Rec_465 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86450 RMVar_ID_86450 Human_SNP_ID_109401816 m1A Human chr2 + 202376554 202376549 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCGGCGGCAG_____GCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCAGCA G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs1330959055 Functional Loss DEL dbSNP153 29..33 33 - - - Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86451 RMVar_ID_86451 Human_SNP_ID_109401817 m1A Human chr2 + 202376551 202376551 202376551 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCT GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCT A G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:202376468..202376596 26863410 MeRIP-seq:(Medium) rs1231549120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4592731 Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86452 RMVar_ID_86452 Human_SNP_ID_109401819 m1A Human chr2 + 202376554 202376554 202376554 GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC GCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCTTCCTCGGGGGGTTGTGATTCGCTCAC A G BMPR2 Ensembl:ENSG00000204217 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:202376507..202376599 26863196 MeRIP-seq:(Medium) rs1258082627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3003275 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 86453 RMVar_ID_86453 Human_SNP_ID_109401827 m1A Human chr2 - 202376572 202376572 202376572 CTCCCGTCAATGGCTCCTGTGAGCGAATCACAACCCCCCGAGGAAGCCGCTGCTGCTGCCGCCGC CTCCCGTCAATGGCTCCTGTGAGCGAATCACACCCCCCCGAGGAAGCCGCTGCTGCTGCCGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:202376376..202376673 26863196 MeRIP-seq:(Medium) rs935220982 Functional Loss SNV dbSNP153 33..33 33 - - - 86454 RMVar_ID_86454 Human_SNP_ID_109467048 m1A Human chr2 - 202635092 202635092 202635092 GAGGATTCTCGAGGCCGGAGGGCAGGCCCCCCAAGACGGGGTGACGAAGCCGGACTCCGGGGTGC GAGGATTCTCGAGGCCGGAGGGCAGGCCCCCCGAGACGGGGTGACGAAGCCGGACTCCGGGGTGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr2:202635000..202635238;chr2:202635001..202635175 26863196,26863410 MeRIP-seq:(Medium) rs1228189999 Functional Loss SNV dbSNP153 33..33 33 - - - 86455 RMVar_ID_86455 Human_SNP_ID_109514399 m1A Human chr2 - 202828983 202828983 202828983 CACTCCATGGATTCCTTTGGGCAACCCAGACCAGAAGATAATCAGTCAGTAGTCAGAAGAATGCA CACTCCATGGATTCCTTTGGGCAACCCAGACCTGAAGATAATCAGTCAGTAGTCAGAAGAATGCA T A ICA1L Ensembl:ENSG00000163596 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:202828932..202829044 26863196 MeRIP-seq:(Medium) rs780586634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_347504,Human_Splice_Rec_347530,Human_Splice_Rec_347554,Human_Splice_Rec_347582,Human_Splice_Rec_347608,Human_Splice_Rec_347628,Human_Splice_Rec_347632,Human_Splice_Rec_347640,Human_Splice_Rec_347650,Human_Splice_Rec_347660,Human_Splice_Rec_347670,Human_Splice_Rec_347680,Human_Splice_Rec_347686,Human_Splice_Rec_347692,Human_Splice_Rec_347702,Human_Splice_Rec_347710,Human_Splice_Rec_347720,Human_Splice_Rec_347728,Human_Splice_Rec_347734 RMVar_hsa_circ_270936,RMVar_hsa_circ_265170,RMVar_hsa_circ_206037,RMVar_hsa_circ_378109,RMVar_hsa_circ_206038,RMVar_hsa_circ_206044,RMVar_hsa_circ_276091,RMVar_hsa_circ_24616,RMVar_hsa_circ_206047,RMVar_hsa_circ_310581,RMVar_hsa_circ_206048,RMVar_hsa_circ_37265,RMVar_hsa_circ_336865,RMVar_hsa_circ_206055,RMVar_hsa_circ_16061,RMVar_hsa_circ_206057,RMVar_hsa_circ_206059,RMVar_hsa_circ_297989,RMVar_hsa_circ_299585,RMVar_hsa_circ_317438,RMVar_hsa_circ_294659,RMVar_hsa_circ_206058,RMVar_hsa_circ_46858,RMVar_hsa_circ_206056,RMVar_hsa_circ_344517,RMVar_hsa_circ_32960,RMVar_hsa_circ_206060,RMVar_hsa_circ_206061 86456 RMVar_ID_86456 Human_SNP_ID_109558893 m1A Human chr2 + 203014924 203014924 203014924 GCTGCGGGGTGACACGGGGCTTCGCCTTGGGAAGGGGTCGAGGGAAGCAGTTAGACGGCTGCCGG GCTGCGGGGTGACACGGGGCTTCGCCTTGGGACGGGGTCGAGGGAAGCAGTTAGACGGCTGCCGG A C NBEAL1 Ensembl:ENSG00000144426 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203014915..203015044 26863196 MeRIP-seq:(Medium) rs998105510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776144,Human_RBP_ID_920814,Human_RBP_ID_18421999,Human_RBP_ID_19002834 Human_Splice_Rec_348103,Human_Splice_Rec_348123,Human_Splice_Rec_348231 RMVar_hsa_circ_206100,RMVar_hsa_circ_104425,RMVar_hsa_circ_116552,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101 86457 RMVar_ID_86457 Human_SNP_ID_109558894 m1A Human chr2 + 203014924 203014924 203014924 GCTGCGGGGTGACACGGGGCTTCGCCTTGGGAAGGGGTCGAGGGAAGCAGTTAGACGGCTGCCGG GCTGCGGGGTGACACGGGGCTTCGCCTTGGGAGGGGGTCGAGGGAAGCAGTTAGACGGCTGCCGG A G NBEAL1 Ensembl:ENSG00000144426 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203014915..203015044 26863196 MeRIP-seq:(Medium) rs998105510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776144,Human_RBP_ID_920814,Human_RBP_ID_18421999,Human_RBP_ID_19002834 Human_Splice_Rec_348103,Human_Splice_Rec_348123,Human_Splice_Rec_348231 RMVar_hsa_circ_206100,RMVar_hsa_circ_104425,RMVar_hsa_circ_116552,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101 86458 RMVar_ID_86458 Human_SNP_ID_109565211 m1A Human chr2 - 203043679 203043679 203043679 TGTCACCCAGGCTGGAGTGCAGTGGCACGATCACAGCACACTACAGCCTCAACTCTCTGGGCCAA TGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCAGCACACTACAGCCTCAACTCTCTGGGCCAA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203043677..203043806 26863196 MeRIP-seq:(Medium) rs1162837990 Functional Loss SNV dbSNP153 33..33 33 - - - 86459 RMVar_ID_86459 Human_SNP_ID_109621026 m1A Human chr2 - 203276480 203276480 203276480 TTCTATATTTCCTGTTGCCTGCCACTTGGTCCAAGCCACATTATCTCTCATGCCTGGTTTATTGC TTCTATATTTCCTGTTGCCTGCCACTTGGTCCTAGCCACATTATCTCTCATGCCTGGTTTATTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:203276476..203276563 26863196 MeRIP-seq:(Medium) rs1268101327 Functional Loss SNV dbSNP153 33..33 33 - - - 86460 RMVar_ID_86460 Human_SNP_ID_109621027 m1A Human chr2 - 203276480 203276480 203276480 TTCTATATTTCCTGTTGCCTGCCACTTGGTCCAAGCCACATTATCTCTCATGCCTGGTTTATTGC TTCTATATTTCCTGTTGCCTGCCACTTGGTCCGAGCCACATTATCTCTCATGCCTGGTTTATTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:203276476..203276563 26863196 MeRIP-seq:(Medium) rs1268101327 Functional Loss SNV dbSNP153 33..33 33 - - - 86461 RMVar_ID_86461 Human_SNP_ID_109659156 m1A Human chr2 + 203422419 203422419 203422419 TAAAGATGGGTGCACTAACTGGGGCGGTGACTATGATGATGGAGAGAAGTCGAGTGTTGGTATTT TAAAGATGGGTGCACTAACTGGGGCGGTGACTCTGATGATGGAGAGAAGTCGAGTGTTGGTATTT A C ABI2 Ensembl:ENSG00000138443 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:203422407..203422541 26863196 MeRIP-seq:(Medium) rs961235349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13745347 RMVar_hsa_circ_285491,RMVar_hsa_circ_206220,RMVar_hsa_circ_305778,RMVar_hsa_circ_307060,RMVar_hsa_circ_337208,RMVar_hsa_circ_206234,RMVar_hsa_circ_206229,RMVar_hsa_circ_266457,RMVar_hsa_circ_270550,RMVar_hsa_circ_206231,RMVar_hsa_circ_275955,RMVar_hsa_circ_206233,RMVar_hsa_circ_274972 86462 RMVar_ID_86462 Human_SNP_ID_109664049 m1A Human chr2 + 203440235 203440235 203440235 GAGGGTCTCTTGGGCTCGGGGTGCTCTGCACCACTGCTGGATTTAATGCTGGAGTTGCGCTGTGG GAGGGTCTCTTGGGCTCGGGGTGCTCTGCACCGCTGCTGGATTTAATGCTGGAGTTGCGCTGTGG A G ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:203440201..203440700 26863196 MeRIP-seq:(Medium) rs6756129 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_27691413 86463 RMVar_ID_86463 Human_SNP_ID_109664125 m1A Human chr2 - 203440400 203440400 203440400 CCTCCTGAAAGCAGCCTGGTGTTTCCTCCTCCACCCCCATCACCTGTCCCAGCCCCACCACCACC CCTCCTGAAAGCAGCCTGGTGTTTCCTCCTCCCCCCCCATCACCTGTCCCAGCCCCACCACCACC T G RAPH1 Ensembl:ENSG00000173166 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203440351..203440700 26863196 MeRIP-seq:(Medium) rs1425961684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638978,Human_RBP_ID_5131677,Human_RBP_ID_17085514,Human_RBP_ID_18948485,Human_RBP_ID_27483060 Human_miRNA_ID_1358748 86464 RMVar_ID_86464 Human_SNP_ID_109664347 m1A Human chr2 + 203440917 203440914 203440918 TAGGAGGAGGTGGGGGGGGTGTTGGGGGAGCCACCTGAGTAATATGCTGAACTTGATGGATCTTC TAGGAGGAGGTGGGGGGGGTGTTGGGGGAG____CTGAGTAATATGCTGAACTTGATGGATCTTC GCCAC G ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:203440868..203441111 26863196 MeRIP-seq:(Medium) rs764401153 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_9428910 86465 RMVar_ID_86465 Human_SNP_ID_109664362 m1A Human chr2 + 203440958 203440958 203440958 ATATGCTGAACTTGATGGATCTTCAGTGGAGGAGGCGGGGCACTGAACTGTGGAAGGGATGGGGC ATATGCTGAACTTGATGGATCTTCAGTGGAGGCGGCGGGGCACTGAACTGTGGAAGGGATGGGGC A C ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:203440908..203440977 26863196 MeRIP-seq:(Medium) rs375823077 Functional Loss SNV dbSNP153 33..33 33 - - - 86466 RMVar_ID_86466 Human_SNP_ID_109664523 m1A Human chr2 + 203441282 203441270 203441282 GGAGGAGGGGGTGGTGGAGGGGGTGGTGGAGGAGGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG GGAGGAGGGGGTGGTGGAGGG____________GGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG GGGTGGTGGAGGA G ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:203441233..203441384 26863196 MeRIP-seq:(Medium) rs770900288 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_8200773 86467 RMVar_ID_86467 Human_SNP_ID_109664534 m1A Human chr2 + 203441282 203441282 203441282 GGAGGAGGGGGTGGTGGAGGGGGTGGTGGAGGAGGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG GGAGGAGGGGGTGGTGGAGGGGGTGGTGGAGGGGGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG A G ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:203441233..203441384 26863196 MeRIP-seq:(Medium) rs777698648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200773 86468 RMVar_ID_86468 Human_SNP_ID_109932771 m1A Human chr2 + 204560738 204560737 204560738 GGAAGGAGTAAGGGTCAAAGCCAGAGTTAAGGAAGCATTTGGGGCAGGATGGAGATATTGTTGGA GGAAGGAGTAAGGGTCAAAGCCAGAGTTAAGG_AGCATTTGGGGCAGGATGGAGATATTGTTGGA GA G PARD3B Ensembl:ENSG00000116117 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:204560587..204560751 26863196 MeRIP-seq:(Medium) rs1215524608 Functional Loss DEL dbSNP153 33..33 33 - - - 86469 RMVar_ID_86469 Human_SNP_ID_110117639 m1A Human chr2 + 205301608 205301608 205301608 AAAAACGAAAGAGAAGGAGAAGAAAAAGGAAAAGGGCAAATTGAAAGTCAAGGAGAAAAAGCGCA AAAAACGAAAGAGAAGGAGAAGAAAAAGGAAAGGGGCAAATTGAAAGTCAAGGAGAAAAAGCGCA A G PARD3B Ensembl:ENSG00000116117 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:205301561..205301756 26863196 MeRIP-seq:(Medium) rs921926162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_349135,Human_Splice_Rec_349221,Human_Splice_Rec_349263,Human_Splice_Rec_349307,Human_Splice_Rec_349343,Human_Splice_Rec_349381,Human_Splice_Rec_349421 RMVar_hsa_circ_70859,RMVar_hsa_circ_53680,RMVar_hsa_circ_35182,RMVar_hsa_circ_118090,RMVar_hsa_circ_94854,RMVar_hsa_circ_85260,RMVar_hsa_circ_206266,RMVar_hsa_circ_109134,RMVar_hsa_circ_206267,RMVar_hsa_circ_206268,RMVar_hsa_circ_107827,RMVar_hsa_circ_206271,RMVar_hsa_circ_206276,RMVar_hsa_circ_81346,RMVar_hsa_circ_206274,RMVar_hsa_circ_99972,RMVar_hsa_circ_206277,RMVar_hsa_circ_206278,RMVar_hsa_circ_309422,RMVar_hsa_circ_345111 86470 RMVar_ID_86470 Human_SNP_ID_110212170 m1A Human chr2 + 205685574 205685574 205685574 GAGCAAATAACACGGCGGTCGCGGCGCGCGGCACCTTGGGCTGGCGCGTGGCTGGGAGGCCGCAT GAGCAAATAACACGGCGGTCGCGGCGCGCGGCTCCTTGGGCTGGCGCGTGGCTGGGAGGCCGCAT A T NRP2 Ensembl:ENSG00000118257 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:205685546..205685657 26863196 MeRIP-seq:(Medium) rs1220194379 Functional Loss SNV dbSNP153 33..33 33 - - - 86471 RMVar_ID_86471 Human_SNP_ID_110227708 m1A Human chr2 - 205751666 205751666 205751666 TAGGGGTGAGGAGGGCTCACCTCATGGGGGGCAGGGCACTGCTGGCGTCAGAGGGAGGAGGAAGA TAGGGGTGAGGAGGGCTCACCTCATGGGGGGCGGGGCACTGCTGGCGTCAGAGGGAGGAGGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:205751661..205751800 26863196 MeRIP-seq:(Medium) rs1208208424 Functional Loss SNV dbSNP153 33..33 33 - - - 86472 RMVar_ID_86472 Human_SNP_ID_110309755 m1A Human chr2 + 206084619 206084618 206084619 CCAAAAAGGAGGGGAAACTCCTACATCTGGGGACTGCTCCAGAAACCCTGCCTGATCCTGCCCCT CCAAAAAGGAGGGGAAACTCCTACATCTGGGG_CTGCTCCAGAAACCCTGCCTGATCCTGCCCCT GA G AC007383.1 Ensembl:ENSG00000227946 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:206084603..206084756 26863196 MeRIP-seq:(Medium) rs1472453099 Functional Loss DEL dbSNP153 33..33 33 - - - 86473 RMVar_ID_86473 Human_SNP_ID_110319222 m1A Human chr2 - 206122202 206122202 206122202 GGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCCTGGACTGCATAGCAA GGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCGGGAGTTCAAGACCAGCCTGGACTGCATAGCAA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1140904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479246 86474 RMVar_ID_86474 Human_SNP_ID_110324854 m1A Human chr2 - 206141952 206141952 206141952 CCACGTTTTGAGGCACCACTGTTTAATGCTAGAATTCGAAAGAGGTTGGTAATAGTATTTATTCA CCACGTTTTGAGGCACCACTGTTTAATGCTAGTATTCGAAAGAGGTTGGTAATAGTATTTATTCA T A NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1801318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3958449,Human_RBP_ID_5528780 Human_Splice_Rec_349795,Human_Splice_Rec_349831,Human_Splice_Rec_349865,Human_Splice_Rec_349893,Human_Splice_Rec_349927,Human_Splice_Rec_349963,Human_Splice_Rec_349993 Clinvar_Rec_466 GWAS_ID_10611,GWAS_ID_10612,GWAS_ID_10613,GWAS_ID_10614,GWAS_ID_10615,GWAS_ID_10616 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_30382,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_281500,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206310,RMVar_hsa_circ_206309,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_298623,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206320,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_325030,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_206321,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326 86475 RMVar_ID_86475 Human_SNP_ID_110324855 m1A Human chr2 - 206141952 206141952 206141952 CCACGTTTTGAGGCACCACTGTTTAATGCTAGAATTCGAAAGAGGTTGGTAATAGTATTTATTCA CCACGTTTTGAGGCACCACTGTTTAATGCTAGGATTCGAAAGAGGTTGGTAATAGTATTTATTCA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1801318 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3958449,Human_RBP_ID_5528780 Human_Splice_Rec_349795,Human_Splice_Rec_349831,Human_Splice_Rec_349865,Human_Splice_Rec_349893,Human_Splice_Rec_349927,Human_Splice_Rec_349963,Human_Splice_Rec_349993 Clinvar_Rec_466 GWAS_ID_10611,GWAS_ID_10612,GWAS_ID_10613,GWAS_ID_10614,GWAS_ID_10615,GWAS_ID_10616 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_30382,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_281500,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206310,RMVar_hsa_circ_206309,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_298623,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206320,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_325030,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_206321,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326 86476 RMVar_ID_86476 Human_SNP_ID_110324887 m1A Human chr2 - 206142052 206142052 206142052 ATATTGTATTTCTAGCACAGATTTGCGTTCCAATTATCTTCTTAATACTACAATTGCTGGTGTGG ATATTGTATTTCTAGCACAGATTTGCGTTCCATTTATCTTCTTAATACTACAATTGCTGGTGTGG T A NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:206142001..206142075 32194978 MeRIP-seq:(Medium) rs147185691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1021686,Human_RBP_ID_6878984,Human_RBP_ID_17505703,Human_RBP_ID_17948837 Human_Splice_Rec_349794,Human_Splice_Rec_349830,Human_Splice_Rec_349864,Human_Splice_Rec_349892,Human_Splice_Rec_349926,Human_Splice_Rec_349962,Human_Splice_Rec_349992 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_30382,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_281500,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206310,RMVar_hsa_circ_206309,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_298623,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206320,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_325030,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_206321,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326 86477 RMVar_ID_86477 Human_SNP_ID_110324888 m1A Human chr2 - 206142052 206142052 206142052 ATATTGTATTTCTAGCACAGATTTGCGTTCCAATTATCTTCTTAATACTACAATTGCTGGTGTGG ATATTGTATTTCTAGCACAGATTTGCGTTCCAGTTATCTTCTTAATACTACAATTGCTGGTGTGG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:206142001..206142075 32194978 MeRIP-seq:(Medium) rs147185691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1021686,Human_RBP_ID_6878984,Human_RBP_ID_17505703,Human_RBP_ID_17948837 Human_Splice_Rec_349794,Human_Splice_Rec_349830,Human_Splice_Rec_349864,Human_Splice_Rec_349892,Human_Splice_Rec_349926,Human_Splice_Rec_349962,Human_Splice_Rec_349992 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_30382,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_281500,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206310,RMVar_hsa_circ_206309,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_298623,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206320,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_325030,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_206321,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326 86478 RMVar_ID_86478 Human_SNP_ID_110325105 m1A Human chr2 - 206142802 206142802 206142802 TAGTTGCAGAGTTTTCAAGGCAAAGATGTGGCAGCAATTGCAGGTGGCTTGGTGGATGCTGAAGC TAGTTGCAGAGTTTTCAAGGCAAAGATGTGGCTGCAATTGCAGGTGGCTTGGTGGATGCTGAAGC T A NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:206142751..206142825 32194978 MeRIP-seq:(Medium) rs775765672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542966,Human_RBP_ID_922546,Human_RBP_ID_3958450,Human_RBP_ID_8851662,Human_RBP_ID_9296910,Human_RBP_ID_19000560,Human_RBP_ID_22078319,Human_RBP_ID_23850193 Human_Splice_Rec_349792,Human_Splice_Rec_349828,Human_Splice_Rec_349862,Human_Splice_Rec_349890,Human_Splice_Rec_349924,Human_Splice_Rec_349960,Human_Splice_Rec_349990 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_117775,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326,RMVar_hsa_circ_22132,RMVar_hsa_circ_41993,RMVar_hsa_circ_206332 86479 RMVar_ID_86479 Human_SNP_ID_110326380 m1A Human chr2 - 206147620 206147620 206147620 ATGATGTTTGGAAATGATAGGAGCCGATTTTTAGAGGGGAAGCGTGCTGTGGAAGACAAGAACAT ATGATGTTTGGAAATGATAGGAGCCGATTTTTGGAGGGGAAGCGTGCTGTGGAAGACAAGAACAT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:206147569..206147768 26863196 MeRIP-seq:(Medium) rs1424981998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542970,Human_RBP_ID_774479,Human_RBP_ID_827369,Human_RBP_ID_2617582,Human_RBP_ID_3958453,Human_RBP_ID_4593934,Human_RBP_ID_6879005,Human_RBP_ID_8845166,Human_RBP_ID_23850203 Human_Splice_Rec_349784,Human_Splice_Rec_349785,Human_Splice_Rec_349820,Human_Splice_Rec_349821,Human_Splice_Rec_349854,Human_Splice_Rec_349855,Human_Splice_Rec_349882,Human_Splice_Rec_349883,Human_Splice_Rec_349916,Human_Splice_Rec_349917,Human_Splice_Rec_349952,Human_Splice_Rec_349953,Human_Splice_Rec_349982,Human_Splice_Rec_349983,Human_Splice_Rec_350022 RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_268010,RMVar_hsa_circ_264782,RMVar_hsa_circ_305902,RMVar_hsa_circ_280997,RMVar_hsa_circ_206304,RMVar_hsa_circ_206306,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_267152,RMVar_hsa_circ_325297,RMVar_hsa_circ_337316,RMVar_hsa_circ_206317,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_65723,RMVar_hsa_circ_362125,RMVar_hsa_circ_206325,RMVar_hsa_circ_378442,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326,RMVar_hsa_circ_339323,RMVar_hsa_circ_22132,RMVar_hsa_circ_41993,RMVar_hsa_circ_355033,RMVar_hsa_circ_338998,RMVar_hsa_circ_206334,RMVar_hsa_circ_360036,RMVar_hsa_circ_370651,RMVar_hsa_circ_206335 86480 RMVar_ID_86480 Human_SNP_ID_110329477 m1A Human chr2 + 206158241 206158241 206158241 GCCTCGGCCTCCCAAAGTGGTGGGATTACAGGAGTGAGCCACCGCCTCCGGCCTTCAATAGCTTA GCCTCGGCCTCCCAAAGTGGTGGGATTACAGGCGTGAGCCACCGCCTCCGGCCTTCAATAGCTTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:206158238..206158339 26863196 MeRIP-seq:(Medium) rs1265349980 Functional Loss SNV dbSNP153 33..33 33 - - - 86481 RMVar_ID_86481 Human_SNP_ID_110330038 m1A Human chr2 - 206159938 206159938 206159938 TGTATCCGAGAGCTGGGGAGCAGCAGAAAGAGAGCGCGCAAATTGTGGGCGCCCCACGCTGAAGA TGTATCCGAGAGCTGGGGAGCAGCAGAAAGAGGGCGCGCAAATTGTGGGCGCCCCACGCTGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:206159901..206160042;chr2:206159901..206159975 26863196 MeRIP-seq:(Medium) rs1157327686 Functional Loss SNV dbSNP153 33..33 33 - - - 86482 RMVar_ID_86482 Human_SNP_ID_110330364 m1A Human chr2 + 206160709 206160709 206160709 ATCACATCAAGTCTTACGAAAAGGAAAAGGCCAGGTAAAATCATCTTTGTATAGAGCTGAAGAAT ATCACATCAAGTCTTACGAAAAGGAAAAGGCCCGGTAAAATCATCTTTGTATAGAGCTGAAGAAT A C EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:206160676..206160725 26863196 MeRIP-seq:(Medium) rs544198333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2617629 Human_Splice_Rec_350039,Human_Splice_Rec_350051,Human_Splice_Rec_350063,Human_Splice_Rec_350075,Human_Splice_Rec_350089,Human_Splice_Rec_350099,Human_Splice_Rec_350105,Human_Splice_Rec_350109 RMVar_hsa_circ_11942,RMVar_hsa_circ_104041,RMVar_hsa_circ_127163,RMVar_hsa_circ_206340,RMVar_hsa_circ_206341,RMVar_hsa_circ_94738,RMVar_hsa_circ_81688,RMVar_hsa_circ_98237,RMVar_hsa_circ_206342,RMVar_hsa_circ_206343,RMVar_hsa_circ_206344 86483 RMVar_ID_86483 Human_SNP_ID_110330365 m1A Human chr2 + 206160709 206160709 206160709 ATCACATCAAGTCTTACGAAAAGGAAAAGGCCAGGTAAAATCATCTTTGTATAGAGCTGAAGAAT ATCACATCAAGTCTTACGAAAAGGAAAAGGCCGGGTAAAATCATCTTTGTATAGAGCTGAAGAAT A G EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:206160676..206160725 26863196 MeRIP-seq:(Medium) rs544198333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2617629 Human_Splice_Rec_350039,Human_Splice_Rec_350051,Human_Splice_Rec_350063,Human_Splice_Rec_350075,Human_Splice_Rec_350089,Human_Splice_Rec_350099,Human_Splice_Rec_350105,Human_Splice_Rec_350109 RMVar_hsa_circ_11942,RMVar_hsa_circ_104041,RMVar_hsa_circ_127163,RMVar_hsa_circ_206340,RMVar_hsa_circ_206341,RMVar_hsa_circ_94738,RMVar_hsa_circ_81688,RMVar_hsa_circ_98237,RMVar_hsa_circ_206342,RMVar_hsa_circ_206343,RMVar_hsa_circ_206344 86484 RMVar_ID_86484 Human_SNP_ID_110330577 m1A Human chr2 + 206161465 206161465 206161465 TGATGATGACATTGACCTCTTTGGATCTGATGATGAGGAGGTATGGCGTCTTCTATAAAGAACAT TGATGATGACATTGACCTCTTTGGATCTGATGGTGAGGAGGTATGGCGTCTTCTATAAAGAACAT A G EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:206161366..206161469 26863410 MeRIP-seq:(Medium) rs766587437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921702,Human_RBP_ID_9385362,Human_RBP_ID_17965003,Human_RBP_ID_19098603,Human_RBP_ID_26787337 Human_Splice_Rec_350041,Human_Splice_Rec_350053,Human_Splice_Rec_350065,Human_Splice_Rec_350079,Human_Splice_Rec_350091,Human_Splice_Rec_350111 RMVar_hsa_circ_11942,RMVar_hsa_circ_104041,RMVar_hsa_circ_206340,RMVar_hsa_circ_94738,RMVar_hsa_circ_95655,RMVar_hsa_circ_81688,RMVar_hsa_circ_206342,RMVar_hsa_circ_206344,RMVar_hsa_circ_123653,RMVar_hsa_circ_206345,RMVar_hsa_circ_206346 86485 RMVar_ID_86485 Human_SNP_ID_110330578 m1A Human chr2 + 206161465 206161465 206161465 TGATGATGACATTGACCTCTTTGGATCTGATGATGAGGAGGTATGGCGTCTTCTATAAAGAACAT TGATGATGACATTGACCTCTTTGGATCTGATGTTGAGGAGGTATGGCGTCTTCTATAAAGAACAT A T EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:206161366..206161469 26863410 MeRIP-seq:(Medium) rs766587437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921702,Human_RBP_ID_9385362,Human_RBP_ID_17965003,Human_RBP_ID_19098603,Human_RBP_ID_26787337 Human_Splice_Rec_350041,Human_Splice_Rec_350053,Human_Splice_Rec_350065,Human_Splice_Rec_350079,Human_Splice_Rec_350091,Human_Splice_Rec_350111 RMVar_hsa_circ_11942,RMVar_hsa_circ_104041,RMVar_hsa_circ_206340,RMVar_hsa_circ_94738,RMVar_hsa_circ_95655,RMVar_hsa_circ_81688,RMVar_hsa_circ_206342,RMVar_hsa_circ_206344,RMVar_hsa_circ_123653,RMVar_hsa_circ_206345,RMVar_hsa_circ_206346 86486 RMVar_ID_86486 Human_SNP_ID_110330583 m1A Human chr2 + 206161471 206161471 206161471 TGACATTGACCTCTTTGGATCTGATGATGAGGAGGTATGGCGTCTTCTATAAAGAACATATCGGC TGACATTGACCTCTTTGGATCTGATGATGAGGTGGTATGGCGTCTTCTATAAAGAACATATCGGC A T EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:206161392..206161506 26863410 MeRIP-seq:(Medium) rs1178162075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921702,Human_RBP_ID_9385362,Human_RBP_ID_17965003,Human_RBP_ID_19098603,Human_RBP_ID_26787337 Human_Splice_Rec_350041,Human_Splice_Rec_350053,Human_Splice_Rec_350065,Human_Splice_Rec_350079,Human_Splice_Rec_350091,Human_Splice_Rec_350111 RMVar_hsa_circ_11942,RMVar_hsa_circ_104041,RMVar_hsa_circ_206340,RMVar_hsa_circ_94738,RMVar_hsa_circ_95655,RMVar_hsa_circ_81688,RMVar_hsa_circ_206342,RMVar_hsa_circ_206344,RMVar_hsa_circ_123653,RMVar_hsa_circ_206345,RMVar_hsa_circ_206346 86487 RMVar_ID_86487 Human_SNP_ID_110330992 m1A Human chr2 + 206162554 206162554 206162554 TAGATGTGAAACCTTGGGATGATGAGACAGATATGGCGAAATTAGAGGAGTGCGTCAGAAGCATT TAGATGTGAAACCTTGGGATGATGAGACAGATGTGGCGAAATTAGAGGAGTGCGTCAGAAGCATT A G EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:206162526..206162600 32194978 MeRIP-seq:(Medium) rs760925547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542986,Human_RBP_ID_1582744,Human_RBP_ID_1908763,Human_RBP_ID_3612768,Human_RBP_ID_9101403,Human_RBP_ID_13753281,Human_RBP_ID_23892928 Human_Splice_Rec_350044,Human_Splice_Rec_350045,Human_Splice_Rec_350056,Human_Splice_Rec_350057,Human_Splice_Rec_350082,Human_Splice_Rec_350083,Human_Splice_Rec_350094,Human_Splice_Rec_350095,Human_Splice_Rec_350114,Human_Splice_Rec_350115,Human_Splice_Rec_350117 Human_miRNA_ID_1388937,Human_miRNA_ID_2707895,Human_miRNA_ID_2707896 RMVar_hsa_circ_94738,RMVar_hsa_circ_95655,RMVar_hsa_circ_206342,RMVar_hsa_circ_206346 86488 RMVar_ID_86488 Human_SNP_ID_110565051 m1A Human chr2 - 207120733 207120733 207120733 AAGGTGTATGGAGATGGGAATTCAGGTTGGAAAGAGGCTGCTGATACAAGGACTGGAGTTGGGAG AAGGTGTATGGAGATGGGAATTCAGGTTGGAAGGAGGCTGCTGATACAAGGACTGGAGTTGGGAG T C KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:207120688..207120768 26863196 MeRIP-seq:(Medium) rs150397779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206387,RMVar_hsa_circ_302534,RMVar_hsa_circ_379046,RMVar_hsa_circ_206388 86489 RMVar_ID_86489 Human_SNP_ID_110571795 m1A Human chr2 + 207148819 207148819 207148819 ATACTGTGCCTTCCTCACTCACTGACATTACCAGGCTGACTCCCCGGGGCCATCTTTATGACTCC ATACTGTGCCTTCCTCACTCACTGACATTACCGGGCTGACTCCCCGGGGCCATCTTTATGACTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:207148790..207148915 26863196 MeRIP-seq:(Medium) rs759755414 Functional Loss SNV dbSNP153 33..33 33 - - - 86490 RMVar_ID_86490 Human_SNP_ID_110575948 m1A Human chr2 + 207165915 207165915 207165915 CGTGGATCAGGAAGGGGGATGCAAACTCACTGACACGAAGCTGCCATCTATTTCTGCAGCGCTGT CGTGGATCAGGAAGGGGGATGCAAACTCACTGGCACGAAGCTGCCATCTATTTCTGCAGCGCTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:207165592..207166003 26863196 MeRIP-seq:(Medium) rs1199427670 Functional Loss SNV dbSNP153 33..33 33 - - - 86491 RMVar_ID_86491 Human_SNP_ID_110575970 m1A Human chr2 - 207165974 207165970 207165975 TCGCGAGAGAAAAAAATGCAACCTCCCAAAATAAAGAGCAAAGATTGCATTAGGAGCGAACAGCG TCGCGAGAGAAAAAAATGCAACCTCCCAAAA_____AGCAAAGATTGCATTAGGAGCGAACAGCG TCTTTA T KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:207165688..207165997 26863196 MeRIP-seq:(Medium) rs1009749578 Functional Loss DEL dbSNP153 32..36 33 - - - Human_Splice_Rec_350743,Human_Splice_Rec_350751 86492 RMVar_ID_86492 Human_SNP_ID_110575971 m1A Human chr2 - 207165974 207165971 207165975 TCGCGAGAGAAAAAAATGCAACCTCCCAAAATAAAGAGCAAAGATTGCATTAGGAGCGAACAGCG TCGCGAGAGAAAAAAATGCAACCTCCCAAAA____GAGCAAAGATTGCATTAGGAGCGAACAGCG CTTTA C KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:207165688..207165997 26863196 MeRIP-seq:(Medium) rs1322271875 Functional Loss DEL dbSNP153 32..35 33 - - - Human_Splice_Rec_350743,Human_Splice_Rec_350751 86493 RMVar_ID_86493 Human_SNP_ID_110576309 m1A Human chr2 + 207166607 207166607 207166607 GGTCGGGAGGTGAAAGGCCGGAGTGCGGGGTCAGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGG GGTCGGGAGGTGAAAGGCCGGAGTGCGGGGTCGGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGG A G MYOSLID Ensembl:ENSG00000229647 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:207166557..207166850 26863196 MeRIP-seq:(Medium) rs1198087966 Functional Loss SNV dbSNP153 33..33 33 - - - 86494 RMVar_ID_86494 Human_SNP_ID_110576310 m1A Human chr2 + 207166607 207166607 207166607 GGTCGGGAGGTGAAAGGCCGGAGTGCGGGGTCAGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGG GGTCGGGAGGTGAAAGGCCGGAGTGCGGGGTCTGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGG A T MYOSLID Ensembl:ENSG00000229647 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:207166557..207166850 26863196 MeRIP-seq:(Medium) rs1198087966 Functional Loss SNV dbSNP153 33..33 33 - - - 86495 RMVar_ID_86495 Human_SNP_ID_110576316 m1A Human chr2 + 207166621 207166621 207166621 AGGCCGGAGTGCGGGGTCAGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGGGCCGCGGGGAAGCC AGGCCGGAGTGCGGGGTCAGGACGCCTCCTGGCGGGGGCGCGGCGCAGGGGGCCGCGGGGAAGCC A C MYOSLID Ensembl:ENSG00000229647 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:207166597..207166750 26863196 MeRIP-seq:(Medium) rs1170191075 Functional Loss SNV dbSNP153 33..33 33 - - - 86496 RMVar_ID_86496 Human_SNP_ID_110576322 m1A Human chr2 + 207166635 207166635 207166635 GGTCAGGACGCCTCCTGGAGGGGGCGCGGCGCAGGGGGCCGCGGGGAAGCCGCCGAGGGCGCGGA GGTCAGGACGCCTCCTGGAGGGGGCGCGGCGCGGGGGGCCGCGGGGAAGCCGCCGAGGGCGCGGA A G MYOSLID Ensembl:ENSG00000229647 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:207166407..207166845 26863196 MeRIP-seq:(Medium) rs1051745346 Functional Loss SNV dbSNP153 33..33 33 - - - 86497 RMVar_ID_86497 Human_SNP_ID_110576336 m1A Human chr2 + 207166674 207166674 207166674 CGCGGGGAAGCCGCCGAGGGCGCGGAGCGGGAAGGAAGGACAGTGGCCACCCCGCCTCCGCCTGG CGCGGGGAAGCCGCCGAGGGCGCGGAGCGGGAGGGAAGGACAGTGGCCACCCCGCCTCCGCCTGG A G MYOSLID Ensembl:ENSG00000229647 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:207166593..207166792 26863196 MeRIP-seq:(Medium) rs1007005593 Functional Loss SNV dbSNP153 33..33 33 - - - 86498 RMVar_ID_86498 Human_SNP_ID_110657048 m1A Human chr2 - 207530125 207530125 207530125 CCTCCTCCTCCTGCTCCTCTTACCGGTGGTACAAGCTCCTCCGTCACTGCTTTCGTTCACGGCCC CCTCCTCCTCCTGCTCCTCTTACCGGTGGTACGAGCTCCTCCGTCACTGCTTTCGTTCACGGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:207529951..207530375 26863196 MeRIP-seq:(Medium) rs1400840042 Functional Loss SNV dbSNP153 33..33 33 - - - 86499 RMVar_ID_86499 Human_SNP_ID_110663856 m1A Human chr2 - 207555629 207555629 207555629 TTCTCGGCTCCAGATTCCATGGTCATTTAGTTACCTATAATAATATGGAAGAGTGTTACAAGCAC TTCTCGGCTCCAGATTCCATGGTCATTTAGTTGCCTATAATAATATGGAAGAGTGTTACAAGCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:207555626..207555700 26863196 MeRIP-seq:(Medium) rs772288583 Functional Loss SNV dbSNP153 33..33 33 - - - 86500 RMVar_ID_86500 Human_SNP_ID_110679697 m1A Human chr2 + 207621823 207621823 207621823 ATGCATGACACTCACCCAGCAGGGCAGCCACTATGCCCACCAGCCCCGTGCCAGCACCCAGCTCC ATGCATGACACTCACCCAGCAGGGCAGCCACTGTGCCCACCAGCCCCGTGCCAGCACCCAGCTCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:207621801..207621900 32194978 MeRIP-seq:(Medium) rs1289083576 Functional Loss SNV dbSNP153 33..33 33 - - - 86501 RMVar_ID_86501 Human_SNP_ID_110680643 m1A Human chr2 - 207625169 207625169 207625169 GCTCACGGCGCCCCGTATGGCCTGGGGATCCTAAGAGGCCCTGTGACCCCCCTCGCCTGGTCTCC GCTCACGGCGCCCCGTATGGCCTGGGGATCCTGAGAGGCCCTGTGACCCCCCTCGCCTGGTCTCC T C METTL21A Ensembl:ENSG00000144401 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:207625158..207625247 26863410 MeRIP-seq:(Medium) rs1435391670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624991 86502 RMVar_ID_86502 Human_SNP_ID_110703926 m1A Human chr2 + 207711695 207711695 207711695 GCGGCGGCAGCGCGGCGGTGGGGGTGCGGCCGAGGCCCGAGCCCTGCCCGGGGCCGGGCCGCGGG GCGGCGGCAGCGCGGCGGTGGGGGTGCGGCCGGGGCCCGAGCCCTGCCCGGGGCCGGGCCGCGGG A G CCNYL1 Ensembl:ENSG00000163249 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:207711638..207711887 26863196 MeRIP-seq:(Medium) rs1450097455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777322,Human_RBP_ID_4622830,Human_RBP_ID_9428915,Human_RBP_ID_18422007,Human_RBP_ID_18470886,Human_RBP_ID_18948499,Human_RBP_ID_22451706 86503 RMVar_ID_86503 Human_SNP_ID_110718886 m1A Human chr2 - 207769750 207769750 207769750 GAGCGTCGCCACCGCCCCCAGGAGTCCACTGGAGCGCGGAGCCCCCTGCAGGGGAGGAGGCGAGC GAGCGTCGCCACCGCCCCCAGGAGTCCACTGGGGCGCGGAGCCCCCTGCAGGGGAGGAGGCGAGC T C FZD5 Ensembl:ENSG00000163251 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:207769700..207769899 26863196 MeRIP-seq:(Medium) rs1038068608 Functional Loss SNV dbSNP153 33..33 33 - - - 86504 RMVar_ID_86504 Human_SNP_ID_110718902 m1A Human chr2 - 207769796 207769796 207769796 AAGGGTGCGAGAGCGCGGGGGAGGAGCCGAGCAGGGCACGTCCCGAGAGCGTCGCCACCGCCCCC AAGGGTGCGAGAGCGCGGGGGAGGAGCCGAGCGGGGCACGTCCCGAGAGCGTCGCCACCGCCCCC T C FZD5 Ensembl:ENSG00000163251 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:207769753..207769844 26863196 MeRIP-seq:(Medium) rs1357463340 Functional Loss SNV dbSNP153 33..33 33 - - - 86505 RMVar_ID_86505 Human_SNP_ID_110769171 m1A Human chr2 - 207985116 207985116 207985116 GATGGAAAGATGGTGGAGTTAAGAGTGGCAGCACTGTGTGAGGGGTTCCTGAGGAAATTTATGAT GATGGAAAGATGGTGGAGTTAAGAGTGGCAGCGCTGTGTGAGGGGTTCCTGAGGAAATTTATGAT T C PLEKHM3 Ensembl:ENSG00000178385 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:207985114..207985185 26863196 MeRIP-seq:(Medium) rs1263857036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71363,RMVar_hsa_circ_360030 86506 RMVar_ID_86506 Human_SNP_ID_110772663 m1A Human chr2 - 208001950 208001950 208001950 TGTTATCCTGTTTATTTTCTTCCAGGAAATCAAGGATTGGCGTGGCATTGCTTTGACAAGTACTT TGTTATCCTGTTTATTTTCTTCCAGGAAATCACGGATTGGCGTGGCATTGCTTTGACAAGTACTT T G PLEKHM3 Ensembl:ENSG00000178385 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:208001871..208001988 26863196 MeRIP-seq:(Medium) rs978214650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22505011 Human_Splice_Rec_351134,Human_Splice_Rec_351162 RMVar_hsa_circ_71363,RMVar_hsa_circ_360030,RMVar_hsa_circ_206429,RMVar_hsa_circ_306224 86507 RMVar_ID_86507 Human_SNP_ID_110838133 m1A Human chr2 - 208255084 208255084 208255084 GACAAAGCCGGGAAGAGGAAAAGCTCGGACCTACCCTGTGGTCCCGGGTTTCTGCAGAGTCTACT GACAAAGCCGGGAAGAGGAAAAGCTCGGACCTGCCCTGTGGTCCCGGGTTTCTGCAGAGTCTACT T C IDH1 Ensembl:ENSG00000138413 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:208255024..208255106 26863410 MeRIP-seq:(Medium) rs753267741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5501596,Human_RBP_ID_9101581 86508 RMVar_ID_86508 Human_SNP_ID_110840800 m1A Human chr2 + 208266322 208266322 208266322 CCTGCCGCAACCGTCCGCGGCCTGAGGAGCCCACCGCCGCTCTCGGGGGCCGACTTCCGGGGGCT CCTGCCGCAACCGTCCGCGGCCTGAGGAGCCCGCCGCCGCTCTCGGGGGCCGACTTCCGGGGGCT A G PIKFYVE Ensembl:ENSG00000115020 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:208266274..208271612 26863196 MeRIP-seq:(Medium) rs1034797233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625010,Human_RBP_ID_8852182,Human_RBP_ID_9296922 Human_Splice_Rec_351361,Human_Splice_Rec_351443,Human_Splice_Rec_351461,Human_Splice_Rec_351497,Human_Splice_Rec_351519,Human_Splice_Rec_351539,Human_Splice_Rec_351551 RMVar_hsa_circ_84345,RMVar_hsa_circ_116175,RMVar_hsa_circ_206437,RMVar_hsa_circ_206438 86509 RMVar_ID_86509 Human_SNP_ID_110840821 m1A Human chr2 - 208266354 208266354 208266354 GCCCCCCGCCCCAGCCTCCGCTTCAACGGCTCAGCCCCCGGAAGTCGGCCCCCGAGAGCGGCGGT GCCCCCCGCCCCAGCCTCCGCTTCAACGGCTCGGCCCCCGGAAGTCGGCCCCCGAGAGCGGCGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:208266307..208266437 26863196 MeRIP-seq:(Medium) rs984542217 Functional Loss SNV dbSNP153 33..33 33 - - - 86510 RMVar_ID_86510 Human_SNP_ID_110842198 m1A Human chr2 + 208271476 208271476 208271476 CTGTTTGGAATCAACTTTTGAGCTTCCTGAGGAATTTAGATTTTTGCTTGTTTCTTTTGTTTTTC CTGTTTGGAATCAACTTTTGAGCTTCCTGAGGTATTTAGATTTTTGCTTGTTTCTTTTGTTTTTC A T PIKFYVE Ensembl:ENSG00000115020 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:208271472..208271569 26863196 MeRIP-seq:(Medium) rs749619705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84345,RMVar_hsa_circ_116175,RMVar_hsa_circ_206437,RMVar_hsa_circ_206438 86511 RMVar_ID_86511 Human_SNP_ID_484009566 m1A Human chr11 - 120111437 120111437 120111437 TTGCATATCAGGGTGCTCAAGGATTGGAGAGGAGACAAAACCAGGAGCAGCACAGTGGGGACATC TTGCATATCAGGGTGCTCAAGGATTGGAGAGGGGACAAAACCAGGAGCAGCACAGTGGGGACATC T C TRIM29 Ensembl:ENSG00000137699 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:120111388..120111467 26863196 MeRIP-seq:(Medium) rs1210648839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79737,RMVar_hsa_circ_86270,RMVar_hsa_circ_89155,RMVar_hsa_circ_83529,RMVar_hsa_circ_153565,RMVar_hsa_circ_153567,RMVar_hsa_circ_76042,RMVar_hsa_circ_153568,RMVar_hsa_circ_153566,RMVar_hsa_circ_153564 86512 RMVar_ID_86512 Human_SNP_ID_484011947 m1A Human chr11 + 120120460 120120460 120120460 GCCTGGACCCTCCACCCATCCTAGCTTCCCACATTCATCTCACACTGGGGTCCCAGCCCTGTGCC GCCTGGACCCTCCACCCATCCTAGCTTCCCACCTTCATCTCACACTGGGGTCCCAGCCCTGTGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:120120458..120120555 26863196 MeRIP-seq:(Medium) rs1043036580 Functional Loss SNV dbSNP153 33..33 33 - - - 86513 RMVar_ID_86513 Human_SNP_ID_484013594 m1A Human chr11 - 120125806 120125806 120125806 TATCATGTCCTGCTGGAGGGGGAGGGCCTGGGACAGTCACTAGGCAACTTCAAGGACGACCTGCT TATCATGTCCTGCTGGAGGGGGAGGGCCTGGGCCAGTCACTAGGCAACTTCAAGGACGACCTGCT T G TRIM29 Ensembl:ENSG00000137699 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:120125755..120125821 26863196 MeRIP-seq:(Medium) rs1441631896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1308962,Human_Splice_Rec_1309048,Human_Splice_Rec_1309066 Human_miRNA_ID_2037352,Human_miRNA_ID_2348056 RMVar_hsa_circ_86270,RMVar_hsa_circ_375657,RMVar_hsa_circ_153564,RMVar_hsa_circ_153569 86514 RMVar_ID_86514 Human_SNP_ID_484014032 m1A Human chr11 - 120127427 120127427 120127427 GGATGCTGTGGACCAAGTGAAGGTGATCATGGATGCTCTGGATGAGAGAGCCAAGGTGCTGCATG GGATGCTGTGGACCAAGTGAAGGTGATCATGGTTGCTCTGGATGAGAGAGCCAAGGTGCTGCATG T A TRIM29 Ensembl:ENSG00000137699 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:120127376..120128563 26863196 MeRIP-seq:(Medium) rs773903788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1308961,Human_Splice_Rec_1309047,Human_Splice_Rec_1309065 RMVar_hsa_circ_86270,RMVar_hsa_circ_153564 86515 RMVar_ID_86515 Human_SNP_ID_484014259 m1A Human chr11 + 120128351 120128351 120128351 AAATGGGAGCCAAGGCCTGCGTCTTTCCAGGCAGGCCAGGTCGGGTAAGGGAGCAGCAAGGTGAG AAATGGGAGCCAAGGCCTGCGTCTTTCCAGGCGGGCCAGGTCGGGTAAGGGAGCAGCAAGGTGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:120128348..120128433 26863196 MeRIP-seq:(Medium) rs1316891886 Functional Loss SNV dbSNP153 33..33 33 - - - 86516 RMVar_ID_86516 Human_SNP_ID_484014294 m1A Human chr11 - 120128416 120128416 120128416 GATTGAGGATGAAGCTGAGAAGTGGCAGAAGGAGAAGGACCGCATCAAGGTGAGCAGCCCCCAAG GATTGAGGATGAAGCTGAGAAGTGGCAGAAGGTGAAGGACCGCATCAAGGTGAGCAGCCCCCAAG T A TRIM29 Ensembl:ENSG00000137699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:120128401..120128500 26863196 MeRIP-seq:(Medium) rs144558232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1308958,Human_Splice_Rec_1308959,Human_Splice_Rec_1309044,Human_Splice_Rec_1309045,Human_Splice_Rec_1309062,Human_Splice_Rec_1309063,Human_Splice_Rec_1309089 RMVar_hsa_circ_86270,RMVar_hsa_circ_153564 86517 RMVar_ID_86517 Human_SNP_ID_484014295 m1A Human chr11 - 120128416 120128416 120128416 GATTGAGGATGAAGCTGAGAAGTGGCAGAAGGAGAAGGACCGCATCAAGGTGAGCAGCCCCCAAG GATTGAGGATGAAGCTGAGAAGTGGCAGAAGGGGAAGGACCGCATCAAGGTGAGCAGCCCCCAAG T C TRIM29 Ensembl:ENSG00000137699 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:120128401..120128500 26863196 MeRIP-seq:(Medium) rs144558232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1308958,Human_Splice_Rec_1308959,Human_Splice_Rec_1309044,Human_Splice_Rec_1309045,Human_Splice_Rec_1309062,Human_Splice_Rec_1309063,Human_Splice_Rec_1309089 RMVar_hsa_circ_86270,RMVar_hsa_circ_153564 86518 RMVar_ID_86518 Human_SNP_ID_484014383 m1A Human chr11 - 120128638 120128638 120128638 GCATGGTGCCTGGCATATCCGAGGTCCTGATGAATGTTTGCTGAATGAAGAGCTGAATAGATGAG GCATGGTGCCTGGCATATCCGAGGTCCTGATGGATGTTTGCTGAATGAAGAGCTGAATAGATGAG T C TRIM29 Ensembl:ENSG00000137699 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:120128597..120128787 26863196 MeRIP-seq:(Medium) rs913671421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86270,RMVar_hsa_circ_153564 86519 RMVar_ID_86519 Human_SNP_ID_484016419 m1A Human chr11 + 120137299 120137299 120137299 ATGATTCTTGTGCTCCTGGAACATGCAAAGGTAGCAGATGCAGGTCTGGTCGGTCTGGCAGAAGA ATGATTCTTGTGCTCCTGGAACATGCAAAGGTGGCAGATGCAGGTCTGGTCGGTCTGGCAGAAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:120137276..120137300 26863196 MeRIP-seq:(Medium) rs747222379 Functional Loss SNV dbSNP153 33..33 33 - - - 86520 RMVar_ID_86520 Human_SNP_ID_484034000 m1A Human chr11 + 120211037 120211037 120211037 GAAAAGTGCAAAACACAGGCTCGCAGCGCTGGAGCCCGGGGCCGCGGAGCCGGGCCGGGGCAGCG GAAAAGTGCAAAACACAGGCTCGCAGCGCTGGCGCCCGGGGCCGCGGAGCCGGGCCGGGGCAGCG A C OAF Ensembl:ENSG00000184232 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:120210986..120211174;chr11:120210935..120211195 26863196 MeRIP-seq:(Medium) rs1332854206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184473,Human_RBP_ID_5111269,Human_RBP_ID_22434033 86521 RMVar_ID_86521 Human_SNP_ID_484034027 m1A Human chr11 + 120211144 120211144 120211144 TACCCACGTGCGTCCGCGCCACCTCGCGGGCGACCCCGCGGCCAAGGCCCCCGGCGGAGCGGCTC TACCCACGTGCGTCCGCGCCACCTCGCGGGCGTCCCCGCGGCCAAGGCCCCCGGCGGAGCGGCTC A T OAF Ensembl:ENSG00000184232 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:120211044..120211186 26863410 MeRIP-seq:(Medium) rs1333133385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184474,Human_RBP_ID_22434034 86522 RMVar_ID_86522 Human_SNP_ID_484034472 m1A Human chr11 + 120212425 120212425 120212425 CAGGAAATGGGCCTGGATGGTGAGTGACTAACAGTGACCCAGCAGCAGGAAAGCTGGAGGAAAAG CAGGAAATGGGCCTGGATGGTGAGTGACTAACCGTGACCCAGCAGCAGGAAAGCTGGAGGAAAAG A C OAF Ensembl:ENSG00000184232 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:120212410..120212524 26863196 MeRIP-seq:(Medium) rs1306253308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9415702 86523 RMVar_ID_86523 Human_SNP_ID_484034502 m1A Human chr11 + 120212565 120212565 120212565 TCTGTCCCTGGGGGAGTGCAGGGGTGAAGCCGATTAGATAGCTGGGGGAGCCCGGGGCCCCGGGG TCTGTCCCTGGGGGAGTGCAGGGGTGAAGCCGTTTAGATAGCTGGGGGAGCCCGGGGCCCCGGGG A T OAF Ensembl:ENSG00000184232 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:120212561..120212670 26863196 MeRIP-seq:(Medium) rs1023470516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17185099 86524 RMVar_ID_86524 Human_SNP_ID_484065046 m1A Human chr11 + 120336794 120336794 120336794 ACGCTGCGGCCACGAGCAGCCGGCAGCCCCAGATAGAGAGCCGGGAGGGAGGGCCCCGGCCCTTG ACGCTGCGGCCACGAGCAGCCGGCAGCCCCAGTTAGAGAGCCGGGAGGGAGGGCCCCGGCCCTTG A T ARHGEF12 Ensembl:ENSG00000196914 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:120336456..120337050 26863196 MeRIP-seq:(Medium) rs950767445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4188512 86525 RMVar_ID_86525 Human_SNP_ID_484065062 m1A Human chr11 - 120336840 120336840 120336840 TCGGCTCCTCCTCCGGAGTCTCGGGGCCTCGAACTCCCCGCCGCGGCAAGGGCCGGGGCCCTCCC TCGGCTCCTCCTCCGGAGTCTCGGGGCCTCGACCTCCCCGCCGCGGCAAGGGCCGGGGCCCTCCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:120336479..120336938 26863410 MeRIP-seq:(Medium) rs1057469487 Functional Loss SNV dbSNP153 33..33 33 - - - 86526 RMVar_ID_86526 Human_SNP_ID_484091133 m1A Human chr11 - 120449201 120449201 120449201 ACTTCAAACTTCAACATACTTGCACTGTTGTCATGACGGCTTGGTCTCCGTGGGGGTCCCAGGAT ACTTCAAACTTCAACATACTTGCACTGTTGTCCTGACGGCTTGGTCTCCGTGGGGGTCCCAGGAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:120449151..120449225 32194978 MeRIP-seq:(Medium) rs766034313 Functional Loss SNV dbSNP153 33..33 33 - - - 86527 RMVar_ID_86527 Human_SNP_ID_484098672 m1A Human chr11 - 120480384 120480384 120480384 TTAACATCCTTCTCTTCCTTGTTAACTGCTCCATCACCTTCTGATGGATTCTCATCACTATGTGC TTAACATCCTTCTCTTCCTTGTTAACTGCTCCGTCACCTTCTGATGGATTCTCATCACTATGTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:120478377..120481326 32194978 MeRIP-seq:(Medium) rs909297728 Functional Loss SNV dbSNP153 33..33 33 - - - 86528 RMVar_ID_86528 Human_SNP_ID_484100119 m1A Human chr11 - 120485794 120485794 120485794 GTTGAGGATTCCTATTAATTGTGGTTGATCCCAGCTACAGAGAAGAGGTGCTTGCCTCAGGGCGG GTTGAGGATTCCTATTAATTGTGGTTGATCCCGGCTACAGAGAAGAGGTGCTTGCCTCAGGGCGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:120485743..120485844 32194978 MeRIP-seq:(Medium) rs1565522615 Functional Loss SNV dbSNP153 33..33 33 - - - 86529 RMVar_ID_86529 Human_SNP_ID_484100121 m1A Human chr11 + 120485802 120485802 120485802 AGGCAAGCACCTCTTCTCTGTAGCTGGGATCAACCACAATTAATAGGAATCCTCAACATACTAAA AGGCAAGCACCTCTTCTCTGTAGCTGGGATCAGCCACAATTAATAGGAATCCTCAACATACTAAA A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:120485751..120485825 32194978 MeRIP-seq:(Medium) rs1165122083 Functional Loss SNV dbSNP153 33..33 33 - - - 86530 RMVar_ID_86530 Human_SNP_ID_484100220 m1A Human chr11 + 120486266 120486266 120486266 CTGATGGTGCCAAAGGGCCCTGAGTCAAAAGGATAGCCAAGGGTGGAGTGGAAAAAGATATGGTG CTGATGGTGCCAAAGGGCCCTGAGTCAAAAGGGTAGCCAAGGGTGGAGTGGAAAAAGATATGGTG A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:120486142..120486343 32194978 MeRIP-seq:(Medium) rs550015084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8175378,Human_RBP_ID_26409084 Human_miRNA_ID_1056707 86531 RMVar_ID_86531 Human_SNP_ID_484232317 m1A Human chr11 + 121036480 121036480 121036480 TTTTGGTTGTTTTTGTTGCTGAAAGTATATGCAAAGTGTTTTTGTCTTATATTTCAGAATGTCTA TTTTGGTTGTTTTTGTTGCTGAAAGTATATGCTAAGTGTTTTTGTCTTATATTTCAGAATGTCTA A T TBCEL,AP000646.1 Ensembl:ENSG00000154114,Ensembl:ENSG00000285509 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:121036475..121045767 26863196 MeRIP-seq:(Medium) rs1015926007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23490756 RMVar_hsa_circ_153657,RMVar_hsa_circ_368741,RMVar_hsa_circ_296390 86532 RMVar_ID_86532 Human_SNP_ID_484490565 m1A Human chr11 - 122105752 122105752 122105752 GTGTTTAAGATTCCGATGGGGGAGGGAAAGCCATTGATTGGGCCTTTGAAACCATGCCAGGAACC GTGTTTAAGATTCCGATGGGGGAGGGAAAGCCGTTGATTGGGCCTTTGAAACCATGCCAGGAACC T C MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:122105595..122105823 26863196 MeRIP-seq:(Medium) rs940558182 Functional Loss SNV dbSNP153 33..33 33 - - - 86533 RMVar_ID_86533 Human_SNP_ID_484513304 m1A Human chr11 - 122202720 122202720 122202720 CAAGAGGACAGTCGTGACGGGGGGAGGAGCGGATGGAGCATTCACAAAAGGTGGTCAGCAGAGAT CAAGAGGACAGTCGTGACGGGGGGAGGAGCGGTTGGAGCATTCACAAAAGGTGGTCAGCAGAGAT T A MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:122202574..122202739 26863196 MeRIP-seq:(Medium) rs554025290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288329,RMVar_hsa_circ_363961,RMVar_hsa_circ_153741,RMVar_hsa_circ_153742,RMVar_hsa_circ_153747,RMVar_hsa_circ_308149,RMVar_hsa_circ_153746 86534 RMVar_ID_86534 Human_SNP_ID_484519986 m1A Human chr11 - 122232026 122232026 122232026 AAAGGAGAGCAAAAGGCAGACCGACGGAAAGAAGGAGAGCCAGGAGAAAGTGGCGTCTCAGAGAC AAAGGAGAGCAAAAGGCAGACCGACGGAAAGAGGGAGAGCCAGGAGAAAGTGGCGTCTCAGAGAC T C MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:122231979..122232077;chr11:122231977..122232122 26863196 MeRIP-seq:(Medium) rs1430751758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288329,RMVar_hsa_circ_363961,RMVar_hsa_circ_308149,RMVar_hsa_circ_360573 86535 RMVar_ID_86535 Human_SNP_ID_484542916 m1A Human chr11 - 122330305 122330305 122330305 CTGTGAACACAGTTATTCTCATAGACTTAGGAAGAAAGGAAGGATTCGGGGTGAACGGGTAGGGA CTGTGAACACAGTTATTCTCATAGACTTAGGAGGAAAGGAAGGATTCGGGGTGAACGGGTAGGGA T C MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:122330301..122330537 26863196 MeRIP-seq:(Medium) rs1001192351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2294716,Human_RBP_ID_5553827 86536 RMVar_ID_86536 Human_SNP_ID_484543537 m1A Human chr11 - 122333202 122333202 122333202 AGAAAGAAAGAAATGAAGAAGAAAAAAGTGAAAAACAGAATGAGGTGGGAAAGGAAAGAGAAGGG AGAAAGAAAGAAATGAAGAAGAAAAAAGTGAATAACAGAATGAGGTGGGAAAGGAAAGAGAAGGG T A MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:122333200..122333277 26863196 MeRIP-seq:(Medium) rs1016160734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2294723 86537 RMVar_ID_86537 Human_SNP_ID_484553139 m1A Human chr11 + 122372816 122372816 122372816 AATCAGAGTGAATATACTTCACCTCCCCTTCTATTACTATGGATGAACTGTCCATCCTCCCGCAG AATCAGAGTGAATATACTTCACCTCCCCTTCTGTTACTATGGATGAACTGTCCATCCTCCCGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:122372797..122372901 26863196 MeRIP-seq:(Medium) rs140443080 Functional Loss SNV dbSNP153 33..33 33 - - - 86538 RMVar_ID_86538 Human_SNP_ID_484556229 m1A Human chr11 + 122385547 122385547 122385547 GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCAGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCCGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:122385501..122385700;chr11:122385498..122385733 26863196 MeRIP-seq:(Medium) rs934066104 Functional Loss SNV dbSNP153 33..33 33 - - - 86539 RMVar_ID_86539 Human_SNP_ID_484556230 m1A Human chr11 + 122385547 122385547 122385547 GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCAGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCGGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:122385501..122385700;chr11:122385498..122385733 26863196 MeRIP-seq:(Medium) rs934066104 Functional Loss SNV dbSNP153 33..33 33 - - - 86540 RMVar_ID_86540 Human_SNP_ID_484556231 m1A Human chr11 + 122385547 122385547 122385547 GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCAGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA GCCAAAGTCCTTACTGTGTCCTACAAGGTCCCTGGTTCTCCCCTCTCTTTACCTTTCTTATCTCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:122385501..122385700;chr11:122385498..122385733 26863196 MeRIP-seq:(Medium) rs934066104 Functional Loss SNV dbSNP153 33..33 33 - - - 86541 RMVar_ID_86541 Human_SNP_ID_484556241 m1A Human chr11 + 122385603 122385600 122385604 CTTATCTCACTTCCTCCTAGTCCCCACTCCTCAGTCTTTCCATTTCTCTCATCCTGACCTCCTTG CTTATCTCACTTCCTCCTAGTCCCCACTCC____TCTTTCCATTTCTCTCATCCTGACCTCCTTG CTCAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:122385527..122385713 26863196 MeRIP-seq:(Medium) rs1301976650 Functional Loss DEL dbSNP153 31..34 33 - - - 86542 RMVar_ID_86542 Human_SNP_ID_484720633 m1A Human chr11 + 123058255 123058255 123058255 GAGGAAAAAAAAAAAAAAAAAACACAAACCTGATTCTTATCAAGCCAGTTGATAATTTCATTACA GAGGAAAAAAAAAAAAAAAAAACACAAACCTGTTTCTTATCAAGCCAGTTGATAATTTCATTACA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:123058251..123058521 32194978 MeRIP-seq:(Medium) rs1480815795 Functional Loss SNV dbSNP153 33..33 33 - - - 86543 RMVar_ID_86543 Human_SNP_ID_484720809 m1A Human chr11 + 123058619 123058619 123058619 AAATACCATTATCCCTGTCAAGACCAGATGACAGTGCCTCCTTACCCTTGTCATTAGTGATAGTA AAATACCATTATCCCTGTCAAGACCAGATGACGGTGCCTCCTTACCCTTGTCATTAGTGATAGTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:123058617..123058749 26863196 MeRIP-seq:(Medium) rs765230787 Functional Loss SNV dbSNP153 33..33 33 - - - 86544 RMVar_ID_86544 Human_SNP_ID_484720810 m1A Human chr11 + 123058619 123058619 123058619 AAATACCATTATCCCTGTCAAGACCAGATGACAGTGCCTCCTTACCCTTGTCATTAGTGATAGTA AAATACCATTATCCCTGTCAAGACCAGATGACTGTGCCTCCTTACCCTTGTCATTAGTGATAGTA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:123058617..123058749 26863196 MeRIP-seq:(Medium) rs765230787 Functional Loss SNV dbSNP153 33..33 33 - - - 86545 RMVar_ID_86545 Human_SNP_ID_484721679 m1A Human chr11 - 123060611 123060611 123060611 TCTATGGTTCTGACAAAGATGAAGGAAATTGCAGAAGCCTACCTTGGGAAGGTGAGGTTGGTTTT TCTATGGTTCTGACAAAGATGAAGGAAATTGCGGAAGCCTACCTTGGGAAGGTGAGGTTGGTTTT T C HSPA8 Ensembl:ENSG00000109971 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs769361497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22435695,Human_RBP_ID_22753909,Human_RBP_ID_24363264 Human_Splice_Rec_1311193,Human_Splice_Rec_1311223,Human_Splice_Rec_1311239,Human_Splice_Rec_1311255,Human_Splice_Rec_1311279,Human_Splice_Rec_1311315,Human_Splice_Rec_1311323,Human_Splice_Rec_1311331,Human_Splice_Rec_1311336,Human_Splice_Rec_1311337,Human_Splice_Rec_1311349,Human_Splice_Rec_1311355,Human_Splice_Rec_1311361,Human_Splice_Rec_1311367 RMVar_hsa_circ_69907,RMVar_hsa_circ_76803,RMVar_hsa_circ_153775,RMVar_hsa_circ_45331,RMVar_hsa_circ_104646,RMVar_hsa_circ_110331,RMVar_hsa_circ_153782,RMVar_hsa_circ_97307,RMVar_hsa_circ_153784,RMVar_hsa_circ_101424,RMVar_hsa_circ_153786,RMVar_hsa_circ_153785,RMVar_hsa_circ_45414,RMVar_hsa_circ_46909,RMVar_hsa_circ_63817,RMVar_hsa_circ_65069 86546 RMVar_ID_86546 Human_SNP_ID_484721937 m1A Human chr11 - 123061203 123061203 123061203 CAATGATCAGGGAAACCGAACCACTCCAAGCTATGTCGCCTTTACGGACACTGAACGGTTGATCG CAATGATCAGGGAAACCGAACCACTCCAAGCTGTGTCGCCTTTACGGACACTGAACGGTTGATCG T C HSPA8 Ensembl:ENSG00000109971 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123061153..123061253 26863196 MeRIP-seq:(Medium) rs765012279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29763,Human_RBP_ID_390954,Human_RBP_ID_1454842,Human_RBP_ID_1776484,Human_RBP_ID_2255333,Human_RBP_ID_3370168,Human_RBP_ID_4188678,Human_RBP_ID_8346169,Human_RBP_ID_8767828,Human_RBP_ID_9363087,Human_RBP_ID_11549341,Human_RBP_ID_17463540,Human_RBP_ID_18604313,Human_RBP_ID_19580896,Human_RBP_ID_22753917,Human_RBP_ID_23491241,Human_RBP_ID_24459054,Human_RBP_ID_26401834,Human_RBP_ID_26804208,Human_RBP_ID_26887102,Human_RBP_ID_27198960 Human_Splice_Rec_1311191,Human_Splice_Rec_1311207,Human_Splice_Rec_1311221,Human_Splice_Rec_1311237,Human_Splice_Rec_1311253,Human_Splice_Rec_1311277,Human_Splice_Rec_1311303,Human_Splice_Rec_1311313,Human_Splice_Rec_1311320,Human_Splice_Rec_1311321,Human_Splice_Rec_1311329,Human_Splice_Rec_1311335,Human_Splice_Rec_1311343,Human_Splice_Rec_1311347,Human_Splice_Rec_1311353,Human_Splice_Rec_1311359,Human_Splice_Rec_1311365,Human_Splice_Rec_1311371,Human_Splice_Rec_1311375 RMVar_hsa_circ_69907,RMVar_hsa_circ_76803,RMVar_hsa_circ_153775,RMVar_hsa_circ_45331,RMVar_hsa_circ_104646,RMVar_hsa_circ_110331,RMVar_hsa_circ_153782,RMVar_hsa_circ_97307,RMVar_hsa_circ_153784,RMVar_hsa_circ_101424,RMVar_hsa_circ_153786,RMVar_hsa_circ_153785,RMVar_hsa_circ_153788,RMVar_hsa_circ_45414,RMVar_hsa_circ_63817,RMVar_hsa_circ_65069,RMVar_hsa_circ_372970 86547 RMVar_ID_86547 Human_SNP_ID_484722398 m1A Human chr11 + 123062053 123062048 123062053 ACGCTCCCAGACCCACAACCCAACTCTTGAGCAGAGGTTTTACCTGGGGTGTAGGCCTGGCTCCA ACGCTCCCAGACCCACAACCCAACTCTT_____GAGGTTTTACCTGGGGTGTAGGCCTGGCTCCA TGAGCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123062051..123062150 26863196 MeRIP-seq:(Medium) rs1005371957 Functional Loss DEL dbSNP153 29..33 33 - - - 86548 RMVar_ID_86548 Human_SNP_ID_484722429 m1A Human chr11 - 123062078 123062078 123062078 GGTTTTTTGTGGCTTCCTTCGTTATTGGAGCCAGGCCTACACCCCAGGTAAAACCTCTGCTCAAG GGTTTTTTGTGGCTTCCTTCGTTATTGGAGCCGGGCCTACACCCCAGGTAAAACCTCTGCTCAAG T C HSPA8 Ensembl:ENSG00000109971 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:123062076..123062150 26863196 MeRIP-seq:(Medium) rs926737538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_390958,Human_RBP_ID_808598,Human_RBP_ID_871642,Human_RBP_ID_986176,Human_RBP_ID_1161204,Human_RBP_ID_1263666,Human_RBP_ID_1454847,Human_RBP_ID_4185460,Human_RBP_ID_5346340,Human_RBP_ID_8767833,Human_RBP_ID_9321810,Human_RBP_ID_9363091,Human_RBP_ID_17791489,Human_RBP_ID_19053323,Human_RBP_ID_22159312,Human_RBP_ID_22434906,Human_RBP_ID_23207133,Human_RBP_ID_24402893,Human_RBP_ID_24459055,Human_RBP_ID_26317891,Human_RBP_ID_26804213,Human_RBP_ID_26887109,Human_RBP_ID_27615529 Human_Splice_Rec_1311205,Human_Splice_Rec_1311219,Human_Splice_Rec_1311235,Human_Splice_Rec_1311301,Human_Splice_Rec_1311311,Human_Splice_Rec_1311319,Human_Splice_Rec_1311333,Human_Splice_Rec_1311341,Human_Splice_Rec_1311377 Human_miRNA_ID_2083520,Human_miRNA_ID_2083521 RMVar_hsa_circ_110331,RMVar_hsa_circ_153784,RMVar_hsa_circ_101424,RMVar_hsa_circ_153785,RMVar_hsa_circ_45414 86549 RMVar_ID_86549 Human_SNP_ID_484722430 m1A Human chr11 - 123062078 123062078 123062078 GGTTTTTTGTGGCTTCCTTCGTTATTGGAGCCAGGCCTACACCCCAGGTAAAACCTCTGCTCAAG GGTTTTTTGTGGCTTCCTTCGTTATTGGAGCCCGGCCTACACCCCAGGTAAAACCTCTGCTCAAG T G HSPA8 Ensembl:ENSG00000109971 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:123062076..123062150 26863196 MeRIP-seq:(Medium) rs926737538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_390958,Human_RBP_ID_808598,Human_RBP_ID_871642,Human_RBP_ID_986176,Human_RBP_ID_1161204,Human_RBP_ID_1263666,Human_RBP_ID_1454847,Human_RBP_ID_4185460,Human_RBP_ID_5346340,Human_RBP_ID_8767833,Human_RBP_ID_9321810,Human_RBP_ID_9363091,Human_RBP_ID_17791489,Human_RBP_ID_19053323,Human_RBP_ID_22159312,Human_RBP_ID_22434906,Human_RBP_ID_23207133,Human_RBP_ID_24402893,Human_RBP_ID_24459055,Human_RBP_ID_26317891,Human_RBP_ID_26804213,Human_RBP_ID_26887109,Human_RBP_ID_27615529 Human_Splice_Rec_1311205,Human_Splice_Rec_1311219,Human_Splice_Rec_1311235,Human_Splice_Rec_1311301,Human_Splice_Rec_1311311,Human_Splice_Rec_1311319,Human_Splice_Rec_1311333,Human_Splice_Rec_1311341,Human_Splice_Rec_1311377 Human_miRNA_ID_2083520,Human_miRNA_ID_2083521 RMVar_hsa_circ_110331,RMVar_hsa_circ_153784,RMVar_hsa_circ_101424,RMVar_hsa_circ_153785,RMVar_hsa_circ_45414 86550 RMVar_ID_86550 Human_SNP_ID_484748088 m1A Human chr11 - 123157942 123157942 123157942 AAAATAATGTAATAAAGAAATGGCTGTGGGGAAGGCAATGGGGCAGTACTGTGTTGGTTCCAAAA AAAATAATGTAATAAAGAAATGGCTGTGGGGAGGGCAATGGGGCAGTACTGTGTTGGTTCCAAAA T C CLMP Ensembl:ENSG00000166250 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:123157930..123158080 26863196 MeRIP-seq:(Medium) rs112840997 Functional Loss SNV dbSNP153 33..33 33 - - - 86551 RMVar_ID_86551 Human_SNP_ID_484816352 m1A Human chr11 + 123432628 123432628 123432628 GAAAACATACTGTGCTGTGTGGTACTGATTGTACTAGAAAAGAGAGAGTTCTGGAGAAGTAGAGG GAAAACATACTGTGCTGTGTGGTACTGATTGTTCTAGAAAAGAGAGAGTTCTGGAGAAGTAGAGG A T GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123432621..123432849 26863196 MeRIP-seq:(Medium) rs1379873628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153793,RMVar_hsa_circ_153794 86552 RMVar_ID_86552 Human_SNP_ID_484819891 m1A Human chr11 + 123446917 123446917 123446917 CAGAGTAAGACCCTGTCTCGGAAGAAAGAAAGAAAAGAAAAGAAAGGAAAGAAAGAAAAAGAAAG CAGAGTAAGACCCTGTCTCGGAAGAAAGAAAGGAAAGAAAAGAAAGGAAAGAAAGAAAAAGAAAG A G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:123446912..123447005 26863196 MeRIP-seq:(Medium) rs558225174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153793,RMVar_hsa_circ_153794 86553 RMVar_ID_86553 Human_SNP_ID_484824808 m1A Human chr11 + 123466323 123466316 123466324 AAAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGAAAGAAAGAAGGAAGGAAGGAAGGAAAGA AAAGAAAGAAAGAGAGAGAGAGAAAG________AGAAAGAAAGAAGGAAGGAAGGAAGGAAAGA GAGAAAGAA G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123466317..123466492 26863196 MeRIP-seq:(Medium) rs145728083 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_153793,RMVar_hsa_circ_153794 86554 RMVar_ID_86554 Human_SNP_ID_484824809 m1A Human chr11 + 123466323 123466316 123466324 AAAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGAAAGAAAGAAGGAAGGAAGGAAGGAAAGA AAAGAAAGAAAGAGAGAGAGAGAAAGAGAA____AGAAAGAAAGAAGGAAGGAAGGAAGGAAAGA GAGAAAGAA GAGAA GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123466317..123466492 26863196 MeRIP-seq:(Medium) rs145728083 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_153793,RMVar_hsa_circ_153794 86555 RMVar_ID_86555 Human_SNP_ID_484824843 m1A Human chr11 + 123466373 123466372 123466374 GGAAGGAAGGAAAGAAGGAAGGAAGGAAAAAGAAAGAGAGAGAGAAAGAAAGAAAAAGAAAGAAA GGAAGGAAGGAAAGAAGGAAGGAAGGAAAAAG__AGAGAGAGAGAAAGAAAGAAAAAGAAAGAAA GAA G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:123466371..123466496 26863196 MeRIP-seq:(Medium) rs35094476 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_153793,RMVar_hsa_circ_153794 86556 RMVar_ID_86556 Human_SNP_ID_484826548 m1A Human chr11 - 123472493 123472493 123472493 TCATGTGTGTCTGTGTCCTTAATTTTCTTGGCATGAGATGACGAACCTTGGGTATTACCCCAGAC TCATGTGTGTCTGTGTCCTTAATTTTCTTGGCGTGAGATGACGAACCTTGGGTATTACCCCAGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123472488..123472570 26863196 MeRIP-seq:(Medium) rs1487590920 Functional Loss SNV dbSNP153 33..33 33 - - - 86557 RMVar_ID_86557 Human_SNP_ID_484830896 m1A Human chr11 - 123490769 123490768 123490769 ATCTGACCCAACCTTCTCTTGCCTCCTCTAAAACTCTGCTTCCTTACCTTTCAATAGATGGCACC ATCTGACCCAACCTTCTCTTGCCTCCTCTAAA_CTCTGCTTCCTTACCTTTCAATAGATGGCACC GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:123490763..123490865 26863196 MeRIP-seq:(Medium) rs1012397143 Functional Loss DEL dbSNP153 33..33 33 - - - 86558 RMVar_ID_86558 Human_SNP_ID_484854243 m1A Human chr11 + 123586134 123586134 123586134 CCTTAGCCTCCGCCTGAGTACTCAGCATAGCGATGGGGTAGAAGCAGATGCTGTCTCTTGGCTGG CCTTAGCCTCCGCCTGAGTACTCAGCATAGCGGTGGGGTAGAAGCAGATGCTGTCTCTTGGCTGG A G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:123586133..123586283 26863196 MeRIP-seq:(Medium) rs1348973802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5167075 RMVar_hsa_circ_77125,RMVar_hsa_circ_371593,RMVar_hsa_circ_153797,RMVar_hsa_circ_342029,RMVar_hsa_circ_153798 86559 RMVar_ID_86559 Human_SNP_ID_484854734 m1A Human chr11 + 123588191 123588191 123588191 ACTGGTTTCTTCCTAGCTGAGATCAATGCCCCACCGAAATCCATCTGTTTTCTCCTGGGCTCCTC ACTGGTTTCTTCCTAGCTGAGATCAATGCCCCGCCGAAATCCATCTGTTTTCTCCTGGGCTCCTC A G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:123588154..123588241 26863410 MeRIP-seq:(Medium) rs757669302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77125,RMVar_hsa_circ_371593,RMVar_hsa_circ_153797,RMVar_hsa_circ_342029,RMVar_hsa_circ_153798 86560 RMVar_ID_86560 Human_SNP_ID_484864912 m1A Human chr11 - 123627504 123627504 123627504 TTGGGGCTGCTCCCTCTGCCTCACCCCACTCCACCCCACGTCAGGATTATCCAGGGGCCACTATG TTGGGGCTGCTCCCTCTGCCTCACCCCACTCCTCCCCACGTCAGGATTATCCAGGGGCCACTATG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:123627455..123627531 26863196 MeRIP-seq:(Medium) rs1482243482 Functional Loss SNV dbSNP153 33..33 33 - - - 86561 RMVar_ID_86561 Human_SNP_ID_484891236 m1A Human chr11 - 123732099 123732096 123732100 GTGGGAATAAAGACAAGACCCGTTAAAAAGAAAGAGAACACACCATGTAGCGTGGAAAGGAGAAG GTGGGAATAAAGACAAGACCCGTTAAAAAGA____GAACACACCATGTAGCGTGGAAAGGAGAAG CTCTT C ZNF202 Ensembl:ENSG00000166261 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:123732097..123732266 26863196 MeRIP-seq:(Medium) rs1458181515 Functional Loss DEL dbSNP153 32..35 33 - - - 86562 RMVar_ID_86562 Human_SNP_ID_484893577 m1A Human chr11 - 123741508 123741508 123741508 TGAGTGGGCTGGGCTGGGCCGGGCCGGGCTGGACCGGGCCGGACCAGATCGGGCAGAGCCGGGCA TGAGTGGGCTGGGCTGGGCCGGGCCGGGCTGGGCCGGGCCGGACCAGATCGGGCAGAGCCGGGCA T C ZNF202 Ensembl:ENSG00000166261 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:123741467..123741614 26863196 MeRIP-seq:(Medium) rs1459505701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88343,RMVar_hsa_circ_153815 86563 RMVar_ID_86563 Human_SNP_ID_485106630 m1A Human chr11 + 124622961 124622961 124622961 GCCCTGCGGTCAGCCCTGGGAACGTCCCGGAGAGCTAGATTCCTAGAGGCCCGATTCCGCTAGCC GCCCTGCGGTCAGCCCTGGGAACGTCCCGGAGGGCTAGATTCCTAGAGGCCCGATTCCGCTAGCC A G TBRG1 Ensembl:ENSG00000154144 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:124622910..124622994 26863196 MeRIP-seq:(Medium) rs372380543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1454862,Human_RBP_ID_4185465,Human_RBP_ID_9363093,Human_RBP_ID_18416680 86564 RMVar_ID_86564 Human_SNP_ID_485110232 m1A Human chr11 - 124636152 124636152 124636152 AATGAAAAGCAAGGGCCAGGTGGGAGTAGCCCAGCGAAGGCACTTGGGCTGCCAGGAACAGGAGG AATGAAAAGCAAGGGCCAGGTGGGAGTAGCCCGGCGAAGGCACTTGGGCTGCCAGGAACAGGAGG T C SIAE Ensembl:ENSG00000110013 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:124636105..124636186 26863196 MeRIP-seq:(Medium) rs140295401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153824,RMVar_hsa_circ_101927 86565 RMVar_ID_86565 Human_SNP_ID_485110235 m1A Human chr11 - 124636167 124636167 124636167 GTGACTGCCCTAAGGAATGAAAAGCAAGGGCCAGGTGGGAGTAGCCCAGCGAAGGCACTTGGGCT GTGACTGCCCTAAGGAATGAAAAGCAAGGGCCCGGTGGGAGTAGCCCAGCGAAGGCACTTGGGCT T G SIAE Ensembl:ENSG00000110013 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:124636118..124636192 26863196 MeRIP-seq:(Medium) rs892977879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153824,RMVar_hsa_circ_101927 86566 RMVar_ID_86566 Human_SNP_ID_485116058 m1A Human chr11 - 124660768 124660768 124660768 ACTCTGATACGTGGATGGTGGTACTGGATCCTATGAAGCCTGGAGGACCTTTCGAAGTGATGGCA ACTCTGATACGTGGATGGTGGTACTGGATCCTTTGAAGCCTGGAGGACCTTTCGAAGTGATGGCA T A SIAE Ensembl:ENSG00000110013 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78778622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1312342,Human_Splice_Rec_1312362,Human_Splice_Rec_1312384,Human_Splice_Rec_1312400,Human_Splice_Rec_1312406 Clinvar_Rec_467 GWAS_ID_10617,GWAS_ID_10618 RMVar_hsa_circ_33541 86567 RMVar_ID_86567 Human_SNP_ID_485116059 m1A Human chr11 - 124660768 124660768 124660768 ACTCTGATACGTGGATGGTGGTACTGGATCCTATGAAGCCTGGAGGACCTTTCGAAGTGATGGCA ACTCTGATACGTGGATGGTGGTACTGGATCCTGTGAAGCCTGGAGGACCTTTCGAAGTGATGGCA T C SIAE Ensembl:ENSG00000110013 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78778622 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1312342,Human_Splice_Rec_1312362,Human_Splice_Rec_1312384,Human_Splice_Rec_1312400,Human_Splice_Rec_1312406 Clinvar_Rec_467 GWAS_ID_10617,GWAS_ID_10618 RMVar_hsa_circ_33541 86568 RMVar_ID_86568 Human_SNP_ID_485119386 m1A Human chr11 + 124675263 124675263 124675263 TCTTTAGGTTCCATAGGCAGTTCTTACCAAGAAGATGTCGATTCCATTCTCCAACACCCACTACC TCTTTAGGTTCCATAGGCAGTTCTTACCAAGATGATGTCGATTCCATTCTCCAACACCCACTACC A T SPA17 Ensembl:ENSG00000064199 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:124675259..124675377;chr11:124675258..124675359 26863196 MeRIP-seq:(Medium) rs1565421901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_391058 Human_Splice_Rec_1312414,Human_Splice_Rec_1312428 86569 RMVar_ID_86569 Human_SNP_ID_485134081 m1A Human chr11 - 124739981 124739981 124739981 GTGGGGGCTCTGGGGCAGTCGGCCGCCAGCCGACCCGCGCCGAAACAGCAGCTCTGCTCTCGGGT GTGGGGGCTCTGGGGCAGTCGGCCGCCAGCCGCCCCGCGCCGAAACAGCAGCTCTGCTCTCGGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:124739926..124746749 26863196 MeRIP-seq:(Medium) rs1481432608 Functional Loss SNV dbSNP153 33..33 33 - - - 86570 RMVar_ID_86570 Human_SNP_ID_485135633 m1A Human chr11 - 124746919 124746919 124746919 GTGGGATAGGGACTTCTCTTCCGGTCAGAGCAAGGGTCGTCCGAAACCAAAACAACCCTCTTCCC GTGGGATAGGGACTTCTCTTCCGGTCAGAGCATGGGTCGTCCGAAACCAAAACAACCCTCTTCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:124746870..124747162 32194978 MeRIP-seq:(Medium) rs1351457268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18604401 86571 RMVar_ID_86571 Human_SNP_ID_485137828 m1A Human chr11 + 124753889 124753880 124753889 GGCCGGAGGGCTCGTGCGGAGGTGACAGAGGAAAGGGTCCCATTCTTGGAGATTGTGTCTGAGCT GGCCGGAGGGCTCGTGCGGAGGTG_________AGGGTCCCATTCTTGGAGATTGTGTCTGAGCT GACAGAGGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:124753786..124753888 26863196 MeRIP-seq:(Medium) rs1196046819 Functional Loss DEL dbSNP153 25..33 33 - - - 86572 RMVar_ID_86572 Human_SNP_ID_485143240 m1A Human chr11 - 124774927 124774927 124774927 TACAGTCGGGTGAAAGAACATGGTGTTGGGAAAAGAAAGAGCAGTTACACATTTGAACAGTTGGA TACAGTCGGGTGAAAGAACATGGTGTTGGGAAGAGAAAGAGCAGTTACACATTTGAACAGTTGGA T C MSANTD2 Ensembl:ENSG00000120458 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:124774817..124774989 26863196 MeRIP-seq:(Medium) rs1006914732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_391126,Human_RBP_ID_26887223 Human_Splice_Rec_1312546 RMVar_hsa_circ_14728 86573 RMVar_ID_86573 Human_SNP_ID_485149008 m1A Human chr11 - 124800013 124800013 124800013 CATCGCAGTGTGGGGCAACGAGCGGCTGGTGGAGGCGCGGTACCAGCAGCTGGAGGGAGCCGGCA CATCGCAGTGTGGGGCAACGAGCGGCTGGTGGGGGCGCGGTACCAGCAGCTGGAGGGAGCCGGCA T C MSANTD2 Ensembl:ENSG00000120458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:124799846..124800116;chr11:124799895..124800208 26863196 MeRIP-seq:(Medium) rs757831254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19605006 86574 RMVar_ID_86574 Human_SNP_ID_485149143 m1A Human chr11 - 124800273 124800273 124800273 GCTTCTCCTGGTGGCCTGAGCGACGGAAATCCATCGCTGTCCGACCCTTCCACGCCTCGGGGTGC GCTTCTCCTGGTGGCCTGAGCGACGGAAATCCGTCGCTGTCCGACCCTTCCACGCCTCGGGGTGC T C MSANTD2 Ensembl:ENSG00000120458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:124800222..124800354 26863196 MeRIP-seq:(Medium) rs1056346112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364400,Human_RBP_ID_17791620,Human_RBP_ID_22159408 86575 RMVar_ID_86575 Human_SNP_ID_485149144 m1A Human chr11 - 124800273 124800273 124800273 GCTTCTCCTGGTGGCCTGAGCGACGGAAATCCATCGCTGTCCGACCCTTCCACGCCTCGGGGTGC GCTTCTCCTGGTGGCCTGAGCGACGGAAATCCCTCGCTGTCCGACCCTTCCACGCCTCGGGGTGC T G MSANTD2 Ensembl:ENSG00000120458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:124800222..124800354 26863196 MeRIP-seq:(Medium) rs1056346112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364400,Human_RBP_ID_17791620,Human_RBP_ID_22159408 86576 RMVar_ID_86576 Human_SNP_ID_485149175 m1A Human chr11 + 124800344 124800344 124800344 AAGCACCTCCATCTTCGGAATTTTTAGCGGCGAGTTGGCGGGCAGCTCCGAGCCACAGGGCGCAG AAGCACCTCCATCTTCGGAATTTTTAGCGGCGGGTTGGCGGGCAGCTCCGAGCCACAGGGCGCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:124800293..124800385 26863196 MeRIP-seq:(Medium) rs1383067924 Functional Loss SNV dbSNP153 33..33 33 - - - 86577 RMVar_ID_86577 Human_SNP_ID_485169476 m1A Human chr11 - 124876545 124876545 124876545 AGGTGCGACCCCTTTCTCCCGACCCGGTCCTCACTCGCCAGCGGCTAAGCCCCTGCCCCTCCCCA AGGTGCGACCCCTTTCTCCCGACCCGGTCCTCCCTCGCCAGCGGCTAAGCCCCTGCCCCTCCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:124876498..124876581 26863196 MeRIP-seq:(Medium) rs1470856892 Functional Loss SNV dbSNP153 33..33 33 - - - 86578 RMVar_ID_86578 Human_SNP_ID_485170282 m1A Human chr11 + 124878642 124878642 124878642 CAATGCCTGAGAGAAGTCACCTGACGGAGCCCAGCTCCAGTGGAGGGTGCCTGGTCACCCCATCC CAATGCCTGAGAGAAGTCACCTGACGGAGCCCGGCTCCAGTGGAGGGTGCCTGGTCACCCCATCC A G ROBO3 Ensembl:ENSG00000154134 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:124878591..124878891 32194978 MeRIP-seq:(Medium) rs1357166145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1312728,Human_Splice_Rec_1312780,Human_Splice_Rec_1312802,Human_Splice_Rec_1312816,Human_Splice_Rec_1312830,Human_Splice_Rec_1312856,Human_Splice_Rec_1312870,Human_Splice_Rec_1312898,Human_Splice_Rec_1312904,Human_Splice_Rec_1312920,Human_Splice_Rec_1312950,Human_Splice_Rec_1312962 86579 RMVar_ID_86579 Human_SNP_ID_485339139 m1A Human chr11 - 125569502 125569502 125569502 CCACCGCAGGCCAGCTCCGCCGGGGCGCTTCCAGGGCCGGGGCCGCTGCGCCCGCACTGGGCATG CCACCGCAGGCCAGCTCCGCCGGGGCGCTTCCGGGGCCGGGGCCGCTGCGCCCGCACTGGGCATG T C FEZ1 Ensembl:ENSG00000149557 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:125569451..125569619 26863196 MeRIP-seq:(Medium) rs1402380004 Functional Loss SNV dbSNP153 33..33 33 - - - 86580 RMVar_ID_86580 Human_SNP_ID_485339153 m1A Human chr11 - 125569527 125569527 125569527 CCGCGGCTCCGGCCCTGCCCCTAGCCCACCGCAGGCCAGCTCCGCCGGGGCGCTTCCAGGGCCGG CCGCGGCTCCGGCCCTGCCCCTAGCCCACCGCGGGCCAGCTCCGCCGGGGCGCTTCCAGGGCCGG T C FEZ1 Ensembl:ENSG00000149557 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:125569476..125569877 26863196 MeRIP-seq:(Medium) rs3017281 Functional Loss SNV dbSNP153 33..33 33 - - - 86581 RMVar_ID_86581 Human_SNP_ID_485339797 m1A Human chr11 - 125572506 125572506 125572506 CTGTCAGCCATCTCTTCACCACCAAACTATCAACTACACACAGGAGAGAGAAGTGTCCCCAAATC CTGTCAGCCATCTCTTCACCACCAAACTATCAGCTACACACAGGAGAGAGAAGTGTCCCCAAATC T C FEZ1 Ensembl:ENSG00000149557 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:125572379..125572525 26863196 MeRIP-seq:(Medium) rs1449890036 Functional Loss SNV dbSNP153 33..33 33 - - - 86582 RMVar_ID_86582 Human_SNP_ID_485339812 m1A Human chr11 + 125572569 125572569 125572569 AGTGTCAAAACCTTTCTCCAGGACCTTGCCAGAGTGAGTACATCTTGTTTATAGGAATTCATCTC AGTGTCAAAACCTTTCTCCAGGACCTTGCCAGGGTGAGTACATCTTGTTTATAGGAATTCATCTC A G EI24 Ensembl:ENSG00000149547 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:125572526..125572575 32194978 MeRIP-seq:(Medium) rs757881648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185470 Human_Splice_Rec_1313765,Human_Splice_Rec_1313779,Human_Splice_Rec_1313797,Human_Splice_Rec_1313817,Human_Splice_Rec_1313835,Human_Splice_Rec_1313855,Human_Splice_Rec_1313865,Human_Splice_Rec_1313877,Human_Splice_Rec_1313899,Human_Splice_Rec_1313919,Human_Splice_Rec_1313937,Human_Splice_Rec_1313945 RMVar_hsa_circ_958,RMVar_hsa_circ_331485,RMVar_hsa_circ_342569,RMVar_hsa_circ_49738,RMVar_hsa_circ_308730,RMVar_hsa_circ_9521,RMVar_hsa_circ_153850 86583 RMVar_ID_86583 Human_SNP_ID_485345125 m1A Human chr11 + 125592917 125592917 125592917 GGAGCCCCGCGGATCGTTTAGGAAAGCCGGCCAGGTGAGAAGGCCGTAGAACGTAACTTGAAAAT GGAGCCCCGCGGATCGTTTAGGAAAGCCGGCCGGGTGAGAAGGCCGTAGAACGTAACTTGAAAAT A G STT3A Ensembl:ENSG00000134910 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr11:125592878..125592982;chr11:125592889..125592974;chr11:125592868..125593419 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1280254577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184490,Human_RBP_ID_5314477,Human_RBP_ID_9321812,Human_RBP_ID_17350401,Human_RBP_ID_17804831,Human_RBP_ID_19050604,Human_RBP_ID_19697677,Human_RBP_ID_22434060,Human_RBP_ID_26317893 Human_Splice_Rec_1313963,Human_Splice_Rec_1313981,Human_Splice_Rec_1314017,Human_Splice_Rec_1314051,Human_Splice_Rec_1314087 86584 RMVar_ID_86584 Human_SNP_ID_485345224 m1A Human chr11 + 125593281 125593281 125593281 GTGGGAAGAAGAGGGAGGTGGGACCCGCTGGAACGACCGGAAGGGAGAAGAGAGTAAAAGATCGT GTGGGAAGAAGAGGGAGGTGGGACCCGCTGGAGCGACCGGAAGGGAGAAGAGAGTAAAAGATCGT A G STT3A Ensembl:ENSG00000134910 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:125593254..125593383 26863196 MeRIP-seq:(Medium) rs1200508794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9415155 86585 RMVar_ID_86585 Human_SNP_ID_485353221 m1A Human chr11 - 125626729 125626729 125626729 CCGAGCACCTCGGCTGTAAAAGGCAGGAATCCAGAAAAGATGTAGAGTGTAAGATCACCAGTGAA CCGAGCACCTCGGCTGTAAAAGGCAGGAATCCTGAAAAGATGTAGAGTGTAAGATCACCAGTGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:125626726..125626850;chr11:125626726..125626877;chr11:125626726..125626895;chr11:125626726..125627702 26863196 MeRIP-seq:(Medium) rs762669601 Functional Loss SNV dbSNP153 33..33 33 - - - 86586 RMVar_ID_86586 Human_SNP_ID_485420029 m1A Human chr11 + 125896232 125896232 125896232 TAAGTCTTTGCACCTCTTGCTCCAGTTCTCGTACTCTTTTTAGGAGCTTCTCAGTCTGGTTTCTG TAAGTCTTTGCACCTCTTGCTCCAGTTCTCGTTCTCTTTTTAGGAGCTTCTCAGTCTGGTTTCTG A T HYLS1 Ensembl:ENSG00000198331 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:125896181..125896274 26863196 MeRIP-seq:(Medium) rs1454739839 Functional Loss SNV dbSNP153 33..33 33 - - - 86587 RMVar_ID_86587 Human_SNP_ID_485498218 m1A Human chr11 - 126205612 126205612 126205612 TGGGAATCATATCTTGATTTCTTTGGCTTCAGATGACATTGTCCCCGAGCTACCGCATGGACGAT TGGGAATCATATCTTGATTTCTTTGGCTTCAGGTGACATTGTCCCCGAGCTACCGCATGGACGAT T C RPUSD4 Ensembl:ENSG00000165526 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126205603..126205668 26863196 MeRIP-seq:(Medium) rs1197407222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866229,Human_RBP_ID_22537913,Human_RBP_ID_22642122 Human_Splice_Rec_1314862,Human_Splice_Rec_1314884,Human_Splice_Rec_1314890,Human_Splice_Rec_1314910 RMVar_hsa_circ_66073,RMVar_hsa_circ_82852,RMVar_hsa_circ_153934,RMVar_hsa_circ_153937,RMVar_hsa_circ_104908,RMVar_hsa_circ_153938 86588 RMVar_ID_86588 Human_SNP_ID_485512613 m1A Human chr11 - 126263460 126263460 126263460 CTCTCCCTAGGATACACAGCCTGCAGGTCCCCAGGACCTGGATGACACCCGCCTCACTGTGGCAG CTCTCCCTAGGATACACAGCCTGCAGGTCCCCGGGACCTGGATGACACCCGCCTCACTGTGGCAG T C SRPRA Ensembl:ENSG00000182934 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126263410..126263509 26863196 MeRIP-seq:(Medium) rs1404107518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_391623,Human_RBP_ID_17234443,Human_RBP_ID_17350429,Human_RBP_ID_22379481,Human_RBP_ID_22754474,Human_RBP_ID_27410044 RMVar_hsa_circ_269827 86589 RMVar_ID_86589 Human_SNP_ID_485512705 m1A Human chr11 - 126263722 126263722 126263722 GCCGCCATCTGCAAGGAAGGCCTAATCATGTTACAATCACTGCCCACTGACCCTCTCCCAGCGGG GCCGCCATCTGCAAGGAAGGCCTAATCATGTTGCAATCACTGCCCACTGACCCTCTCCCAGCGGG T C SRPRA Ensembl:ENSG00000182934 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126263672..126263887 26863196 MeRIP-seq:(Medium) rs990906810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1353822,Human_RBP_ID_17231397,Human_RBP_ID_17347840,Human_RBP_ID_17463679,Human_RBP_ID_17791900,Human_RBP_ID_24459090,Human_RBP_ID_26603119 Human_miRNA_ID_479569,Human_miRNA_ID_629270,Human_miRNA_ID_1502289 RMVar_hsa_circ_269827 86590 RMVar_ID_86590 Human_SNP_ID_485512722 m1A Human chr11 - 126263776 126263776 126263776 AGGCAGAGTGAGGGGGCTTGTGGCTCCTTCCAACCCCACTCCCCGTTCAGCACAGCCGCCATCTG AGGCAGAGTGAGGGGGCTTGTGGCTCCTTCCAGCCCCACTCCCCGTTCAGCACAGCCGCCATCTG T C SRPRA Ensembl:ENSG00000182934 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126263725..126263944 26863196 MeRIP-seq:(Medium) rs1038920486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228064,Human_RBP_ID_751888,Human_RBP_ID_4152573,Human_RBP_ID_17234447,Human_RBP_ID_17350434,Human_RBP_ID_17467057,Human_RBP_ID_17791901,Human_RBP_ID_18188643,Human_RBP_ID_18933053,Human_RBP_ID_23207147,Human_RBP_ID_26410352 RMVar_hsa_circ_269827 86591 RMVar_ID_86591 Human_SNP_ID_485513877 m1A Human chr11 - 126266846 126266846 126266846 AAGTCAGGTCTTCCAGTGGGTCCTGAGAACGGAGTAGAACTTTCCAAAGAGGAGCTGATCCGCAG AAGTCAGGTCTTCCAGTGGGTCCTGAGAACGGCGTAGAACTTTCCAAAGAGGAGCTGATCCGCAG T G SRPRA Ensembl:ENSG00000182934 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:126266745..126266876 26863196 MeRIP-seq:(Medium) rs1345164932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1776732,Human_RBP_ID_6053884,Human_RBP_ID_11554949 Human_Splice_Rec_1315031,Human_Splice_Rec_1315053 RMVar_hsa_circ_153949 86592 RMVar_ID_86592 Human_SNP_ID_485513999 m1A Human chr11 + 126267149 126267149 126267149 CCTTAGCACCGTGTTAACACCTTTCATGTCCCAGTATATCCAAAGAACTCAAACTTGCCTTCCTT CCTTAGCACCGTGTTAACACCTTTCATGTCCCGGTATATCCAAAGAACTCAAACTTGCCTTCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:126267147..126267262 26863196 MeRIP-seq:(Medium) rs1261551978 Functional Loss SNV dbSNP153 33..33 33 - - - 86593 RMVar_ID_86593 Human_SNP_ID_485514589 m1A Human chr11 + 126268822 126268814 126268822 GAAGAAGTCGAGCATGGCGGCAGCGGCAGAGGAGCTGGGGCCGGCGCCGGGAATTCAGGCCGCGT GAAGAAGTCGAGCATGGCGGCAGCG________GCTGGGGCCGGCGCCGGGAATTCAGGCCGCGT GGCAGAGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:126268650..126268872;chr11:126268663..126268860 26863196 MeRIP-seq:(Medium) rs748908902 Functional Loss DEL dbSNP153 26..33 33 - - - 86594 RMVar_ID_86594 Human_SNP_ID_485514791 m1A Human chr11 + 126269207 126269207 126269207 CAGCTTTCAGAGGGTCCGGGCTCAGAGGGGTTATGATTCGGAGGGTTCTGCCGCACGGCATGGGC CAGCTTTCAGAGGGTCCGGGCTCAGAGGGGTTGTGATTCGGAGGGTTCTGCCGCACGGCATGGGC A G FOXRED1 Ensembl:ENSG00000110074 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:126269158..126269289 26863196 MeRIP-seq:(Medium) rs1278923597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752030,Human_RBP_ID_4152657,Human_RBP_ID_8346612,Human_RBP_ID_11554969,Human_RBP_ID_17791920,Human_RBP_ID_18416683,Human_RBP_ID_22035808,Human_RBP_ID_23117994,Human_RBP_ID_23492693 Human_Splice_Rec_1315093,Human_Splice_Rec_1315099,Human_Splice_Rec_1315119,Human_Splice_Rec_1315139,Human_Splice_Rec_1315143,Human_Splice_Rec_1315159,Human_Splice_Rec_1315177,Human_Splice_Rec_1315195,Human_Splice_Rec_1315209 86595 RMVar_ID_86595 Human_SNP_ID_485515399 m1A Human chr11 + 126271396 126271395 126271397 GTGCCCATCCTCCAACCCCCCAACCATGTGGGAAGGAAATGTTTGGCCCTCTGACCCTAACTACA GTGCCCATCCTCCAACCCCCCAACCATGTGGG__GGAAATGTTTGGCCCTCTGACCCTAACTACA GAA G FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126271392..126271490 26863196 MeRIP-seq:(Medium) rs969329860 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1776738,Human_RBP_ID_22572004 86596 RMVar_ID_86596 Human_SNP_ID_485524460 m1A Human chr11 - 126304130 126304130 126304130 TTTCCTCTGTGCTGGCGGCGTGGGCCTCCTCCACGTCCAATTCGCGCTTCCTCTTGCCTAGTTGA TTTCCTCTGTGCTGGCGGCGTGGGCCTCCTCCCCGTCCAATTCGCGCTTCCTCTTGCCTAGTTGA T G AP001318.2 Ensembl:ENSG00000255062 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:126304080..126304200;chr11:126304080..126304209 26863196 MeRIP-seq:(Medium) rs1414440687 Functional Loss SNV dbSNP153 33..33 33 - - - 86597 RMVar_ID_86597 Human_SNP_ID_485524462 m1A Human chr11 + 126304133 126304133 126304133 ACTAGGCAAGAGGAAGCGCGAATTGGACGTGGAGGAGGCCCACGCCGCCAGCACAGAGGAAAAGG ACTAGGCAAGAGGAAGCGCGAATTGGACGTGGCGGAGGCCCACGCCGCCAGCACAGAGGAAAAGG A C DCPS Ensembl:ENSG00000110063 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:126304083..126304174;chr11:126304082..126304316 26863196 MeRIP-seq:(Medium) rs1400312363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185489 86598 RMVar_ID_86598 Human_SNP_ID_485531293 m1A Human chr11 + 126331488 126331488 126331488 ACCTGCGCCAGGACCTCCGCCTGATCCGAGAGACGGGAGATGACTACAGGAATATTACTTTACCC ACCTGCGCCAGGACCTCCGCCTGATCCGAGAGGCGGGAGATGACTACAGGAATATTACTTTACCC A G DCPS Ensembl:ENSG00000110063 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:126331437..126336449 32194978 MeRIP-seq:(Medium) rs759791956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32159,Human_RBP_ID_11555388,Human_RBP_ID_17350438 Human_Splice_Rec_1315334,Human_Splice_Rec_1315335,Human_Splice_Rec_1315346,Human_Splice_Rec_1315347,Human_Splice_Rec_1315353 86599 RMVar_ID_86599 Human_SNP_ID_485535420 m1A Human chr11 - 126348087 126348087 126348087 TCCCATCTCTCTTGCCCCTCAAACATTTATTTATCCGGTGTCAAATTCCTACCCACCTTCCTCCA TCCCATCTCTCTTGCCCCTCAAACATTTATTTCTCCGGTGTCAAATTCCTACCCACCTTCCTCCA T G GSEC Ensembl:ENSG00000280832 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126348054..126348198 26863196 MeRIP-seq:(Medium) rs1342267875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5552340 86600 RMVar_ID_86600 Human_SNP_ID_485537302 m1A Human chr11 - 126355534 126355534 126355534 GGGGAAGGGCGGGGGTGATGCCGCGCGGTCGCAGGCTTGGGATGGTGTTCGCGCCTCCGAGACCC GGGGAAGGGCGGGGGTGATGCCGCGCGGTCGCCGGCTTGGGATGGTGTTCGCGCCTCCGAGACCC T G GSEC Ensembl:ENSG00000280832 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:126355358..126355575 26863196 MeRIP-seq:(Medium) rs538530776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185490,Human_RBP_ID_18416684 Human_Splice_Rec_1315361,Human_Splice_Rec_1315363 86601 RMVar_ID_86601 Human_SNP_ID_485537577 m1A Human chr11 + 126356280 126356280 126356280 TTTGCGGGGTCCGCCTGTGTGCAGGAGTCGCAAGGTCGCTGAGCAGGACCCAAAGGTGGAGTTGT TTTGCGGGGTCCGCCTGTGTGCAGGAGTCGCAGGGTCGCTGAGCAGGACCCAAAGGTGGAGTTGT A G ST3GAL4 Ensembl:ENSG00000110080 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126356275..126356406 26863196 MeRIP-seq:(Medium) rs1270993481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1315431,Human_Splice_Rec_1315451 86602 RMVar_ID_86602 Human_SNP_ID_485542024 m1A Human chr11 - 126373644 126373644 126373644 ACAGCAAAAGAAGTCTCTCTGTTCCCACCCTCAGGCTCCACAGGCTACCCACCACGACCCCCTCC ACAGCAAAAGAAGTCTCTCTGTTCCCACCCTCGGGCTCCACAGGCTACCCACCACGACCCCCTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:126373534..126373673 26863196 MeRIP-seq:(Medium) rs149932521 Functional Loss SNV dbSNP153 33..33 33 - - - 86603 RMVar_ID_86603 Human_SNP_ID_485549140 m1A Human chr11 + 126401909 126401907 126401910 TGAGGGAAGGAGGGAGATGCAGGGGTAGCTTGAGGAGGAGATAGAGCAGAGAGAGGTTTGCTGTT TGAGGGAAGGAGGGAGATGCAGGGGTAGCTT___GAGGAGATAGAGCAGAGAGAGGTTTGCTGTT TGAG T ST3GAL4 Ensembl:ENSG00000110080 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:126401762..126402134 26863196 MeRIP-seq:(Medium) rs1301304740 Functional Loss DEL dbSNP153 32..34 33 - - - 86604 RMVar_ID_86604 Human_SNP_ID_485555362 m1A Human chr11 + 126425226 126425226 126425226 CAGGGGAAGAAGGACACTGAACAGGAGATGGCAGAAGGGGGACTGCGGACCCCAGGAGGGGAGGG CAGGGGAAGAAGGACACTGAACAGGAGATGGCGGAAGGGGGACTGCGGACCCCAGGAGGGGAGGG A G ST3GAL4 Ensembl:ENSG00000110080 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126425198..126425281 26863196 MeRIP-seq:(Medium) rs1324792494 Functional Loss SNV dbSNP153 33..33 33 - - - 86605 RMVar_ID_86605 Human_SNP_ID_485555984 m1A Human chr11 + 126427882 126427882 126427882 CATCCAGGGGAGCAATGATGAGGCCTGAAGTAAAGAAGTGATGGTGGAGGACAGGTGGGGCACAC CATCCAGGGGAGCAATGATGAGGCCTGAAGTACAGAAGTGATGGTGGAGGACAGGTGGGGCACAC A C ST3GAL4 Ensembl:ENSG00000110080 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126427850..126427930 26863196 MeRIP-seq:(Medium) rs1189639952 Functional Loss SNV dbSNP153 33..33 33 - - - 86606 RMVar_ID_86606 Human_SNP_ID_485559758 m1A Human chr11 - 126441555 126441555 126441555 GTATCTGCCATCTAAGTCCCAACTGTGACCCCAGGGATTGGAAAGGGAGCATGACAGTTTCCGTC GTATCTGCCATCTAAGTCCCAACTGTGACCCCCGGGATTGGAAAGGGAGCATGACAGTTTCCGTC T G KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126441505..126441622 26863196 MeRIP-seq:(Medium) rs1241761179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7917,RMVar_hsa_circ_26293 86607 RMVar_ID_86607 Human_SNP_ID_485562114 m1A Human chr11 - 126449077 126449077 126449077 CAGGACCACAGTGGACTACACGTACTTCTCAGAGCCCGTCTCCTGTGAGGTGACCAACGCCCTGG CAGGACCACAGTGGACTACACGTACTTCTCAGCGCCCGTCTCCTGTGAGGTGACCAACGCCCTGG T G KIRREL3 Ensembl:ENSG00000149571 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:126445062..126449087 32194978 MeRIP-seq:(Medium) rs1273562894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1315682,Human_Splice_Rec_1315683,Human_Splice_Rec_1315714,Human_Splice_Rec_1315715,Human_Splice_Rec_1315760,Human_Splice_Rec_1315761 RMVar_hsa_circ_14954,RMVar_hsa_circ_26293,RMVar_hsa_circ_11971,RMVar_hsa_circ_49755 86608 RMVar_ID_86608 Human_SNP_ID_485575625 m1A Human chr11 - 126497215 126497209 126497215 ACACTCACACTGTCTCACACACACTCACTCTCACACACTCACACTCACACACACTCACACTCTCA ACACTCACACTGTCTCACACACACTCACTCTC______TCACACTCACACACACTCACACTCTCA AGTGTGT A KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:126497153..126497282 26863196 MeRIP-seq:(Medium) rs57902579 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_371222,RMVar_hsa_circ_153965 86609 RMVar_ID_86609 Human_SNP_ID_485575626 m1A Human chr11 - 126497215 126497209 126497215 ACACTCACACTGTCTCACACACACTCACTCTCACACACTCACACTCACACACACTCACACTCTCA ACACTCACACTGTCTCACACACACTCACTCTC____ACTCACACTCACACACACTCACACTCTCA AGTGTGT AGT KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:126497153..126497282 26863196 MeRIP-seq:(Medium) rs57902579 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_371222,RMVar_hsa_circ_153965 86610 RMVar_ID_86610 Human_SNP_ID_485575627 m1A Human chr11 - 126497215 126497209 126497215 ACACTCACACTGTCTCACACACACTCACTCTCACACACTCACACTCACACACACTCACACTCTCA ACACTCACACTGTCTCACACACACTCACTCTC__ACACTCACACTCACACACACTCACACTCTCA AGTGTGT AGTGT KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:126497153..126497282 26863196 MeRIP-seq:(Medium) rs57902579 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_371222,RMVar_hsa_circ_153965 86611 RMVar_ID_86611 Human_SNP_ID_485575636 m1A Human chr11 - 126497215 126497215 126497215 ACACTCACACTGTCTCACACACACTCACTCTCACACACTCACACTCACACACACTCACACTCTCA ACACTCACACTGTCTCACACACACTCACTCTCTCACACTCACACTCACACACACTCACACTCTCA T A KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:126497153..126497282 26863196 MeRIP-seq:(Medium) rs57763849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371222,RMVar_hsa_circ_153965 86612 RMVar_ID_86612 Human_SNP_ID_485583162 m1A Human chr11 - 126526651 126526651 126526651 AGTCTATTCCTTCAGCCAGCAGCCCCAGGACCAGGTGGTGGTGTCGGGACAGCCAGTGACGCTAC AGTCTATTCCTTCAGCCAGCAGCCCCAGGACCGGGTGGTGGTGTCGGGACAGCCAGTGACGCTAC T C KIRREL3 Ensembl:ENSG00000149571 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:126526601..126549297 32194978 MeRIP-seq:(Medium) rs1237549156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1315672,Human_Splice_Rec_1315704,Human_Splice_Rec_1315750 RMVar_hsa_circ_371222,RMVar_hsa_circ_153965,RMVar_hsa_circ_286860,RMVar_hsa_circ_329097,RMVar_hsa_circ_153966 86613 RMVar_ID_86613 Human_SNP_ID_485679359 m1A Human chr11 - 126921845 126921845 126921845 TAGATAGATAGGATGACAGAAAGATAGATGATAGATAGATAATAGATAGGAAGGCAGGAAGATAG TAGATAGATAGGATGACAGAAAGATAGATGATGGATAGATAATAGATAGGAAGGCAGGAAGATAG T C KIRREL3,AP002833.1 Ensembl:ENSG00000149571,Ensembl:ENSG00000254938 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126921795..126922087 26863196 MeRIP-seq:(Medium) rs1162466861 Functional Loss SNV dbSNP153 33..33 33 - - - 86614 RMVar_ID_86614 Human_SNP_ID_485679841 m1A Human chr11 + 126923059 126923059 126923059 ATGCCCTCCTGGTTTTCCTCCTCCTTCTCTGGATGTTTCTGCTCAGCTTGCCTTGTGGATCTTCT ATGCCCTCCTGGTTTTCCTCCTCCTTCTCTGGTTGTTTCTGCTCAGCTTGCCTTGTGGATCTTCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126923031..126923192 26863196 MeRIP-seq:(Medium) rs1247640775 Functional Loss SNV dbSNP153 33..33 33 - - - 86615 RMVar_ID_86615 Human_SNP_ID_485679853 m1A Human chr11 - 126923103 126923092 126923104 AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAGGAGAAGAAGAAGAAGAAGATCCACAAGGCAAGCT AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAG____________AAGAAGATCCACAAGGCAAGCT TCTTCTTCTTCTC T KIRREL3,AP002833.1 Ensembl:ENSG00000149571,Ensembl:ENSG00000254938 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126923065..126923166 26863196 MeRIP-seq:(Medium) rs1422096539 Functional Loss DEL dbSNP153 32..43 33 - - - 86616 RMVar_ID_86616 Human_SNP_ID_485679861 m1A Human chr11 - 126923103 126923095 126923104 AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAGGAGAAGAAGAAGAAGAAGATCCACAAGGCAAGCT AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAG_________AAGAAGAAGATCCACAAGGCAAGCT TCTTCTTCTC T KIRREL3,AP002833.1 Ensembl:ENSG00000149571,Ensembl:ENSG00000254938 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126923065..126923166 26863196 MeRIP-seq:(Medium) rs1472148609 Functional Loss DEL dbSNP153 32..40 33 - - - 86617 RMVar_ID_86617 Human_SNP_ID_485679877 m1A Human chr11 - 126923103 126923101 126923104 AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAGGAGAAGAAGAAGAAGAAGATCCACAAGGCAAGCT AGAAGAGAAGAAGGAGAAGGAGAAGGAGAAG___AAGAAGAAGAAGAAGATCCACAAGGCAAGCT TCTC T KIRREL3,AP002833.1 Ensembl:ENSG00000149571,Ensembl:ENSG00000254938 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126923065..126923166 26863196 MeRIP-seq:(Medium) rs1388878602 Functional Loss DEL dbSNP153 32..34 33 - - - 86618 RMVar_ID_86618 Human_SNP_ID_485680418 m1A Human chr11 - 126923330 126923330 126923330 AGAAGGAGAAGGAAGAAGGAGAAGGAGAAGGAAGAAGAAGAAGGAAGAAGGAGAAGGAGAAGGAA AGAAGGAGAAGGAAGAAGGAGAAGGAGAAGGAGGAAGAAGAAGGAAGAAGGAGAAGGAGAAGGAA T C KIRREL3,AP002833.1 Ensembl:ENSG00000149571,Ensembl:ENSG00000254938 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:126923263..126923397 26863196 MeRIP-seq:(Medium) rs1473662653 Functional Loss SNV dbSNP153 33..33 33 - - - 86619 RMVar_ID_86619 Human_SNP_ID_486079529 m1A Human chr11 + 128522155 128522155 128522155 ATTCCCGCTGCCTTTCTTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCACTCCAGGGGAAGTTGG ATTCCCGCTGCCTTTCTTTCCCCCGCGCCCGGGCGGTGCGCGCCCGGCACTCCAGGGGAAGTTGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:128522126..128522349 26863196 MeRIP-seq:(Medium) rs1324748958 Functional Loss SNV dbSNP153 33..33 33 - - - 86620 RMVar_ID_86620 Human_SNP_ID_486079530 m1A Human chr11 + 128522171 128522156 128522171 TTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCACTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT TTTCCCCCGCGCCCGGAC_______________CTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT CGGTGCGCGCCCGGCA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:128522126..128522258 26863196 MeRIP-seq:(Medium) rs1343445502 Functional Loss DEL dbSNP153 19..33 33 - - - 86621 RMVar_ID_86621 Human_SNP_ID_486079539 m1A Human chr11 + 128522171 128522171 128522171 TTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCACTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT TTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCCCTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:128522126..128522258 26863196 MeRIP-seq:(Medium) rs1489327177 Functional Loss SNV dbSNP153 33..33 33 - - - 86622 RMVar_ID_86622 Human_SNP_ID_486079540 m1A Human chr11 + 128522171 128522171 128522171 TTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCACTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT TTTCCCCCGCGCCCGGACGGTGCGCGCCCGGCGCTCCAGGGGAAGTTGGCACTTTGCGGCGAAGT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:128522126..128522258 26863196 MeRIP-seq:(Medium) rs1489327177 Functional Loss SNV dbSNP153 33..33 33 - - - 86623 RMVar_ID_86623 Human_SNP_ID_486079561 m1A Human chr11 - 128522260 128522236 128522260 GGCAGCCGCCGGCGGAGAGGAGGGAGCGGGCGAGGGCCGGGCAGGAGGAGCGGGCGCGGCGCGGG GGCAGCCGCCGGCGGAGAGGAGGGAGCGGGCG________________________CGGCGCGGG GCGCCCGCTCCTCCTGCCCGGCCCT G ETS1 Ensembl:ENSG00000134954 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:128521939..128536441;chr11:128521958..128536441;chr11:128521989..128536441 26863196 MeRIP-seq:(Medium) rs1425455641 Functional Loss DEL dbSNP153 33..56 33 - - - RMVar_hsa_circ_84287,RMVar_hsa_circ_153974 86624 RMVar_ID_86624 Human_SNP_ID_486193870 m1A Human chr11 - 128967837 128967837 128967837 CATGTTTGTTTCTGTTCCTAAACCAGAGTACGAGGTCCCTGGGAATTTAAGTAGCTACGCATTAT CATGTTTGTTTCTGTTCCTAAACCAGAGTACGGGGTCCCTGGGAATTTAAGTAGCTACGCATTAT T C ARHGAP32 Ensembl:ENSG00000134909 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7949524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1263773,Human_RBP_ID_9000419 GWAS_ID_10619,GWAS_ID_10620,GWAS_ID_10621,GWAS_ID_10622,GWAS_ID_10623,GWAS_ID_10624,GWAS_ID_10625,GWAS_ID_10626,GWAS_ID_10627,GWAS_ID_10628,GWAS_ID_10629,GWAS_ID_10630,GWAS_ID_10631,GWAS_ID_10632,GWAS_ID_10633,GWAS_ID_10634,GWAS_ID_10635,GWAS_ID_10636,GWAS_ID_10637,GWAS_ID_10638,GWAS_ID_10639,GWAS_ID_10640,GWAS_ID_10641 86625 RMVar_ID_86625 Human_SNP_ID_486197041 m1A Human chr11 - 128978875 128978875 128978875 CTCAAAATAAGATGAAAAAGTCTCCTGTGGGTAGCTGGCGTTCCTTTTTCAACTTGGGGAAATCA CTCAAAATAAGATGAAAAAGTCTCCTGTGGGTGGCTGGCGTTCCTTTTTCAACTTGGGGAAATCA T C ARHGAP32 Ensembl:ENSG00000134909 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:128978804..128978905 26863196 MeRIP-seq:(Medium) rs752767333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1316548,Human_Splice_Rec_1316570,Human_Splice_Rec_1316592,Human_Splice_Rec_1316632,Human_Splice_Rec_1316650 RMVar_hsa_circ_1338,RMVar_hsa_circ_38460,RMVar_hsa_circ_265356,RMVar_hsa_circ_264994,RMVar_hsa_circ_18090 86626 RMVar_ID_86626 Human_SNP_ID_486225880 m1A Human chr11 - 129100664 129100664 129100664 CTCTGTGCAGTGTTAGTATAAGGGCAGGGTGCAGGCAGGGTTGGGGTTGGCTGGCTCTGCCCACC CTCTGTGCAGTGTTAGTATAAGGGCAGGGTGCGGGCAGGGTTGGGGTTGGCTGGCTCTGCCCACC T C ARHGAP32 Ensembl:ENSG00000134909 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:129100625..129100708 26863196 MeRIP-seq:(Medium) rs1324644183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38460,RMVar_hsa_circ_9611,RMVar_hsa_circ_41496,RMVar_hsa_circ_342798,RMVar_hsa_circ_270657,RMVar_hsa_circ_299465,RMVar_hsa_circ_295412,RMVar_hsa_circ_153993,RMVar_hsa_circ_153994,RMVar_hsa_circ_302956,RMVar_hsa_circ_105347,RMVar_hsa_circ_76898,RMVar_hsa_circ_153998,RMVar_hsa_circ_153999,RMVar_hsa_circ_41517,RMVar_hsa_circ_154000,RMVar_hsa_circ_154004,RMVar_hsa_circ_154001,RMVar_hsa_circ_107210,RMVar_hsa_circ_278015,RMVar_hsa_circ_154002,RMVar_hsa_circ_289494,RMVar_hsa_circ_154005,RMVar_hsa_circ_154003 86627 RMVar_ID_86627 Human_SNP_ID_486416378 m1A Human chr11 - 129869554 129869554 129869554 GGGGCTGCAAGCACCCCCATCAGCATCAGCACAGGAGCCCCCACCGTGCGGCAGGTCCCTGTCAG GGGGCTGCAAGCACCCCCATCAGCATCAGCACTGGAGCCCCCACCGTGCGGCAGGTCCCTGTCAG T A NFRKB Ensembl:ENSG00000170322 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:129869489..129869569 26863196 MeRIP-seq:(Medium) rs779105806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1316789,Human_Splice_Rec_1316837,Human_Splice_Rec_1316889 RMVar_hsa_circ_121082,RMVar_hsa_circ_19172,RMVar_hsa_circ_85437,RMVar_hsa_circ_91115,RMVar_hsa_circ_154014,RMVar_hsa_circ_154015,RMVar_hsa_circ_154013,RMVar_hsa_circ_154017,RMVar_hsa_circ_105574,RMVar_hsa_circ_276332,RMVar_hsa_circ_154016 86628 RMVar_ID_86628 Human_SNP_ID_486416379 m1A Human chr11 - 129869554 129869554 129869554 GGGGCTGCAAGCACCCCCATCAGCATCAGCACAGGAGCCCCCACCGTGCGGCAGGTCCCTGTCAG GGGGCTGCAAGCACCCCCATCAGCATCAGCACGGGAGCCCCCACCGTGCGGCAGGTCCCTGTCAG T C NFRKB Ensembl:ENSG00000170322 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:129869489..129869569 26863196 MeRIP-seq:(Medium) rs779105806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1316789,Human_Splice_Rec_1316837,Human_Splice_Rec_1316889 RMVar_hsa_circ_121082,RMVar_hsa_circ_19172,RMVar_hsa_circ_85437,RMVar_hsa_circ_91115,RMVar_hsa_circ_154014,RMVar_hsa_circ_154015,RMVar_hsa_circ_154013,RMVar_hsa_circ_154017,RMVar_hsa_circ_105574,RMVar_hsa_circ_276332,RMVar_hsa_circ_154016 86629 RMVar_ID_86629 Human_SNP_ID_486416924 m1A Human chr11 + 129871374 129871374 129871374 GCCTTCTCTTTTGAACCCATTCCCCAAAAGCCACCAATCCACTGGCCCAGTGAAGCCCACGCATT GCCTTCTCTTTTGAACCCATTCCCCAAAAGCCCCCAATCCACTGGCCCAGTGAAGCCCACGCATT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:129871324..129872017 26863196 MeRIP-seq:(Medium) rs936532914 Functional Loss SNV dbSNP153 33..33 33 - - - 86630 RMVar_ID_86630 Human_SNP_ID_486417807 m1A Human chr11 - 129874244 129874244 129874244 AGCCAGATGAGCCTCAGTGACTCCAGTATGCCACCCACCCCAGTCACACCTGTAACCCCCACCAC AGCCAGATGAGCCTCAGTGACTCCAGTATGCCTCCCACCCCAGTCACACCTGTAACCCCCACCAC T A NFRKB Ensembl:ENSG00000170322 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:129874193..129874282 26863196 MeRIP-seq:(Medium) rs145578616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1316782,Human_Splice_Rec_1316830,Human_Splice_Rec_1316882,Human_Splice_Rec_1316932 Human_miRNA_ID_2037356,Human_miRNA_ID_2348060,Human_miRNA_ID_2890489 RMVar_hsa_circ_8236,RMVar_hsa_circ_121082,RMVar_hsa_circ_19172,RMVar_hsa_circ_85437,RMVar_hsa_circ_154014,RMVar_hsa_circ_154015,RMVar_hsa_circ_105574,RMVar_hsa_circ_154016 86631 RMVar_ID_86631 Human_SNP_ID_486423235 m1A Human chr11 + 129892827 129892827 129892827 CTCCACACGGACCAAGTTCCAGAGGATCTGTCAGCATATGGTCTAAGGAATCCATTGTTTCTTCT CTCCACACGGACCAAGTTCCAGAGGATCTGTCGGCATATGGTCTAAGGAATCCATTGTTTCTTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:129892778..129892922;chr11:129892776..129892923 26863196 MeRIP-seq:(Medium) rs139713186 Functional Loss SNV dbSNP153 33..33 33 - - - 86632 RMVar_ID_86632 Human_SNP_ID_486423696 m1A Human chr11 - 129894382 129894382 129894382 AGGGAGGACCTGGTCCAGCTTCCCTTCCTCAAATAAGGAAATTGACACCTGGCGTGGTAAGATTT AGGGAGGACCTGGTCCAGCTTCCCTTCCTCAAGTAAGGAAATTGACACCTGGCGTGGTAAGATTT T C NFRKB Ensembl:ENSG00000170322 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:129894351..129894444 26863196 MeRIP-seq:(Medium) rs1565431115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185491,Human_RBP_ID_17598211,Human_RBP_ID_24912867 Human_Splice_Rec_1316745,Human_Splice_Rec_1316843,Human_Splice_Rec_1316895,Human_Splice_Rec_1316952,Human_Splice_Rec_1316953,Human_Splice_Rec_1316966,Human_Splice_Rec_1316967,Human_Splice_Rec_1316982,Human_Splice_Rec_1316983 86633 RMVar_ID_86633 Human_SNP_ID_486424015 m1A Human chr11 + 129895401 129895401 129895401 CCCCACGCCCCGCTCCCGCTCCCCACGCCCACACGGGCAGCGACCTCGCGGACCCAGCCGCCCGC CCCCACGCCCCGCTCCCGCTCCCCACGCCCACCCGGGCAGCGACCTCGCGGACCCAGCCGCCCGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:129895390..129895503 26863196 MeRIP-seq:(Medium) rs1172339577 Functional Loss SNV dbSNP153 33..33 33 - - - 86634 RMVar_ID_86634 Human_SNP_ID_486424063 m1A Human chr11 - 129895519 129895519 129895519 GGGAGCCCGCGGCCGGAGAAGGGCTGCGGGTTAGGGGGCCGGCGCCCGCGGTTCAGGTGAGGGCG GGGAGCCCGCGGCCGGAGAAGGGCTGCGGGTTGGGGGGCCGGCGCCCGCGGTTCAGGTGAGGGCG T C NFRKB Ensembl:ENSG00000170322 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:129895343..129895538;chr11:129895356..129895535;chr11:129894357..129895560 26863196 MeRIP-seq:(Medium) rs1305138449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185492,Human_RBP_ID_18416685,Human_RBP_ID_19050647,Human_RBP_ID_23117996 Human_Splice_Rec_1316941,Human_Splice_Rec_1316951,Human_Splice_Rec_1316965,Human_Splice_Rec_1316981 86635 RMVar_ID_86635 Human_SNP_ID_486424073 m1A Human chr11 - 129895535 129895535 129895535 GGGAGCGAGTGCGTCTGGGAGCCCGCGGCCGGAGAAGGGCTGCGGGTTAGGGGGCCGGCGCCCGC GGGAGCGAGTGCGTCTGGGAGCCCGCGGCCGGGGAAGGGCTGCGGGTTAGGGGGCCGGCGCCCGC T C NFRKB Ensembl:ENSG00000170322 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr11:129895417..129895544;chr11:129895368..129895537 26863196 MeRIP-seq:(Medium) rs555294624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4153092,Human_RBP_ID_18416685,Human_RBP_ID_19050647,Human_RBP_ID_23117996 Human_Splice_Rec_1316941,Human_Splice_Rec_1316951,Human_Splice_Rec_1316965,Human_Splice_Rec_1316981 86636 RMVar_ID_86636 Human_SNP_ID_486430299 m1A Human chr11 - 129920615 129920615 129920615 GAGTGGTGATGCCACGTTCGGGAGATTGGGAGAAGGGGACTGATGGAGGGTGTGGCAAGAGGAAG GAGTGGTGATGCCACGTTCGGGAGATTGGGAGTAGGGGACTGATGGAGGGTGTGGCAAGAGGAAG T A PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:129920581..129920717 26863196 MeRIP-seq:(Medium) rs1171915054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20464,RMVar_hsa_circ_14007,RMVar_hsa_circ_109588,RMVar_hsa_circ_35454,RMVar_hsa_circ_154020,RMVar_hsa_circ_265037,RMVar_hsa_circ_51370,RMVar_hsa_circ_91606,RMVar_hsa_circ_49780,RMVar_hsa_circ_107893,RMVar_hsa_circ_19745,RMVar_hsa_circ_154023,RMVar_hsa_circ_58650,RMVar_hsa_circ_154024 86637 RMVar_ID_86637 Human_SNP_ID_486436946 m1A Human chr11 + 129948303 129948303 129948303 CTGCCCAATTAGCACAAGGTCATACTCAAGCCATGTCCTATTCAATAAATAAAGCAAGTTTTTAA CTGCCCAATTAGCACAAGGTCATACTCAAGCCGTGTCCTATTCAATAAATAAAGCAAGTTTTTAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:129948284..129948512 26863196 MeRIP-seq:(Medium) rs185263969 Functional Loss SNV dbSNP153 33..33 33 - - - 86638 RMVar_ID_86638 Human_SNP_ID_477191459 m1A Human chr11 + 93185811 93185811 93185811 TCTGCTCATTTATCAAGGGCCTCATTACATCCATATCTTTAAAAAAGAAAAACAAAGTACTTCAC TCTGCTCATTTATCAAGGGCCTCATTACATCCGTATCTTTAAAAAAGAAAAACAAAGTACTTCAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:93185776..93185889 26863196 MeRIP-seq:(Medium) rs746309777 Functional Loss SNV dbSNP153 33..33 33 - - - 86639 RMVar_ID_86639 Human_SNP_ID_477191460 m1A Human chr11 - 93185812 93185812 93185812 AGTGAAGTACTTTGTTTTTCTTTTTTAAAGATATGGATGTAATGAGGCCCTTGATAAATGAGCAG AGTGAAGTACTTTGTTTTTCTTTTTTAAAGATGTGGATGTAATGAGGCCCTTGATAAATGAGCAG T C SLC36A4 Ensembl:ENSG00000180773 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:93185751..93197243;chr11:93185726..93197243 26863196 MeRIP-seq:(Medium) rs1200406845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23527130 Human_Splice_Rec_1287430,Human_Splice_Rec_1287452,Human_Splice_Rec_1287488,Human_Splice_Rec_1287500 RMVar_hsa_circ_300678,RMVar_hsa_circ_322788,RMVar_hsa_circ_304489,RMVar_hsa_circ_367629 86640 RMVar_ID_86640 Human_SNP_ID_477194238 m1A Human chr11 - 93197919 93197919 93197919 GAGGCGGGCACCAGGCGCGGGTCCCTCCGGGCAGGGGAGGTAGGCCTGGGCCTGACGCCGGCCAC GAGGCGGGCACCAGGCGCGGGTCCCTCCGGGCTGGGGAGGTAGGCCTGGGCCTGACGCCGGCCAC T A SLC36A4 Ensembl:ENSG00000180773 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:93197717..93197975;chr11:93197730..93197975 26863196 MeRIP-seq:(Medium) rs1251070141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228059,Human_RBP_ID_868273,Human_RBP_ID_4182014,Human_RBP_ID_5344397,Human_RBP_ID_18416643 86641 RMVar_ID_86641 Human_SNP_ID_477194239 m1A Human chr11 - 93197919 93197919 93197919 GAGGCGGGCACCAGGCGCGGGTCCCTCCGGGCAGGGGAGGTAGGCCTGGGCCTGACGCCGGCCAC GAGGCGGGCACCAGGCGCGGGTCCCTCCGGGCGGGGGAGGTAGGCCTGGGCCTGACGCCGGCCAC T C SLC36A4 Ensembl:ENSG00000180773 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:93197717..93197975;chr11:93197730..93197975 26863196 MeRIP-seq:(Medium) rs1251070141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228059,Human_RBP_ID_868273,Human_RBP_ID_4182014,Human_RBP_ID_5344397,Human_RBP_ID_18416643 86642 RMVar_ID_86642 Human_SNP_ID_477259530 m1A Human chr11 - 93479024 93479024 93479024 TCGTGGTGTTTGTGTACGTGGCCACGCGCCCCACCATCACCGAGTGAGCCCCGCAGCCGGCTGCG TCGTGGTGTTTGTGTACGTGGCCACGCGCCCCGCCATCACCGAGTGAGCCCCGCAGCCGGCTGCG T C SMCO4 Ensembl:ENSG00000166002 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:93478980..93479086;chr11:93478980..93479117 26863196 MeRIP-seq:(Medium) rs138064563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86643 RMVar_ID_86643 Human_SNP_ID_477259596 m1A Human chr11 - 93479191 93479190 93479191 TCTGGACACACCCTCCTAGCATCCTCTAGGAAAGATGCGGCAGCTCAAAGGGAAGCCCAAGAAGG TCTGGACACACCCTCCTAGCATCCTCTAGGAA_GATGCGGCAGCTCAAAGGGAAGCCCAAGAAGG CT C SMCO4 Ensembl:ENSG00000166002 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:93479141..93537855 26863196 MeRIP-seq:(Medium) rs773804914 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_406296,Human_RBP_ID_9362834,Human_RBP_ID_23527231 Human_Splice_Rec_1287690,Human_Splice_Rec_1287694,Human_Splice_Rec_1287698,Human_Splice_Rec_1287702,Human_Splice_Rec_1287706 RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86644 RMVar_ID_86644 Human_SNP_ID_477259597 m1A Human chr11 - 93479191 93479191 93479191 TCTGGACACACCCTCCTAGCATCCTCTAGGAAAGATGCGGCAGCTCAAAGGGAAGCCCAAGAAGG TCTGGACACACCCTCCTAGCATCCTCTAGGAAGGATGCGGCAGCTCAAAGGGAAGCCCAAGAAGG T C SMCO4 Ensembl:ENSG00000166002 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:93479141..93537855 26863196 MeRIP-seq:(Medium) rs1370176387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406296,Human_RBP_ID_9362834,Human_RBP_ID_23527231 Human_Splice_Rec_1287690,Human_Splice_Rec_1287694,Human_Splice_Rec_1287698,Human_Splice_Rec_1287702,Human_Splice_Rec_1287706 RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86645 RMVar_ID_86645 Human_SNP_ID_477271355 m1A Human chr11 - 93530682 93530682 93530682 CCTGAAGTGTAGGGACAGTACAATTTGAGTCCATTGTGTCAGGGGAGGAAAGGGAGAGGTTGGGA CCTGAAGTGTAGGGACAGTACAATTTGAGTCCGTTGTGTCAGGGGAGGAAAGGGAGAGGTTGGGA T C SMCO4 Ensembl:ENSG00000166002 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:93530680..93530788 26863196 MeRIP-seq:(Medium) rs1048253288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86646 RMVar_ID_86646 Human_SNP_ID_477271356 m1A Human chr11 - 93530682 93530682 93530682 CCTGAAGTGTAGGGACAGTACAATTTGAGTCCATTGTGTCAGGGGAGGAAAGGGAGAGGTTGGGA CCTGAAGTGTAGGGACAGTACAATTTGAGTCCCTTGTGTCAGGGGAGGAAAGGGAGAGGTTGGGA T G SMCO4 Ensembl:ENSG00000166002 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:93530680..93530788 26863196 MeRIP-seq:(Medium) rs1048253288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86647 RMVar_ID_86647 Human_SNP_ID_477274790 m1A Human chr11 - 93543343 93543343 93543343 GCGCCGAGAGGAGAGGCGAGGCGGGGAGCGCAAGCGGCGGCGGCCACTGCCACGTATTCCCGGCA GCGCCGAGAGGAGAGGCGAGGCGGGGAGCGCACGCGGCGGCGGCCACTGCCACGTATTCCCGGCA T G SMCO4 Ensembl:ENSG00000166002 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:93543228..93543380 26863196 MeRIP-seq:(Medium) rs1305040032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184372 Human_Splice_Rec_1287691,Human_Splice_Rec_1287703 RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 86648 RMVar_ID_86648 Human_SNP_ID_477303796 m1A Human chr11 - 93661735 93661735 93661735 CCCGGGGCCTGGACACAGTAACCGCAGCTCAGAGCAAGCCAGCCTGGTAAGCTCCTGCCCATCAG CCCGGGGCCTGGACACAGTAACCGCAGCTCAGGGCAAGCCAGCCTGGTAAGCTCCTGCCCATCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:93661642..93661808 26863196 MeRIP-seq:(Medium) rs1159433218 Functional Loss SNV dbSNP153 33..33 33 - - - 86649 RMVar_ID_86649 Human_SNP_ID_477305179 m1A Human chr11 + 93667806 93667806 93667806 TATGGGAGAGGGACATCGACAGGCCAAAGAAAATGTGAGTGAGATCTTATTTGACTACCCTGTTG TATGGGAGAGGGACATCGACAGGCCAAAGAAAGTGTGAGTGAGATCTTATTTGACTACCCTGTTG A G CEP295 Ensembl:ENSG00000166004 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:93667769..93667853 26863196 MeRIP-seq:(Medium) rs988038294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868275,Human_RBP_ID_3939797,Human_RBP_ID_9362836,Human_RBP_ID_18974858,Human_RBP_ID_26320537,Human_RBP_ID_27803899 Human_Splice_Rec_1287711 RMVar_hsa_circ_12356,RMVar_hsa_circ_89988,RMVar_hsa_circ_308170,RMVar_hsa_circ_307016,RMVar_hsa_circ_50583,RMVar_hsa_circ_65090,RMVar_hsa_circ_16993,RMVar_hsa_circ_152453,RMVar_hsa_circ_152454 86650 RMVar_ID_86650 Human_SNP_ID_477305180 m1A Human chr11 + 93667806 93667806 93667806 TATGGGAGAGGGACATCGACAGGCCAAAGAAAATGTGAGTGAGATCTTATTTGACTACCCTGTTG TATGGGAGAGGGACATCGACAGGCCAAAGAAATTGTGAGTGAGATCTTATTTGACTACCCTGTTG A T CEP295 Ensembl:ENSG00000166004 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:93667769..93667853 26863196 MeRIP-seq:(Medium) rs988038294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868275,Human_RBP_ID_3939797,Human_RBP_ID_9362836,Human_RBP_ID_18974858,Human_RBP_ID_26320537,Human_RBP_ID_27803899 Human_Splice_Rec_1287711 RMVar_hsa_circ_12356,RMVar_hsa_circ_89988,RMVar_hsa_circ_308170,RMVar_hsa_circ_307016,RMVar_hsa_circ_50583,RMVar_hsa_circ_65090,RMVar_hsa_circ_16993,RMVar_hsa_circ_152453,RMVar_hsa_circ_152454 86651 RMVar_ID_86651 Human_SNP_ID_477324123 m1A Human chr11 - 93739328 93739328 93739328 GTCATATTTACTAAATTTCATAATTTCAGAAAACTGTTTAAAACAAAGAGCAATTGATGGATAAA GTCATATTTACTAAATTTCATAATTTCAGAAAGCTGTTTAAAACAAAGAGCAATTGATGGATAAA T C TAF1D Ensembl:ENSG00000166012 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:93739251..93739350;chr11:93739251..93739389 26863196 MeRIP-seq:(Medium) rs766599519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406425,Human_RBP_ID_1783905,Human_RBP_ID_2292095,Human_RBP_ID_8062774,Human_RBP_ID_9008214,Human_RBP_ID_9362855,Human_RBP_ID_11750130,Human_RBP_ID_23207434,Human_RBP_ID_23268076,Human_RBP_ID_24909355,Human_RBP_ID_27620670 Human_Splice_Rec_1287836,Human_Splice_Rec_1287837,Human_Splice_Rec_1287858,Human_Splice_Rec_1287859,Human_Splice_Rec_1287960,Human_Splice_Rec_1287961,Human_Splice_Rec_1288006,Human_Splice_Rec_1288007,Human_Splice_Rec_1288018,Human_Splice_Rec_1288019,Human_Splice_Rec_1288024,Human_Splice_Rec_1288025,Human_Splice_Rec_1288030,Human_Splice_Rec_1288034 RMVar_hsa_circ_328217,RMVar_hsa_circ_23363,RMVar_hsa_circ_40960,RMVar_hsa_circ_53558 86652 RMVar_ID_86652 Human_SNP_ID_477324883 m1A Human chr11 - 93741431 93741431 93741431 TGGTTATCGGGAGTTGGAGGGCTGAGGTCGGGAGGGTGGTGTGTACAGAGCTCTAGGACACCAGG TGGTTATCGGGAGTTGGAGGGCTGAGGTCGGGGGGGTGGTGTGTACAGAGCTCTAGGACACCAGG T C TAF1D Ensembl:ENSG00000166012 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr11:93741301..93741475;chr11:93741331..93741467 26863196 MeRIP-seq:(Medium) rs571146220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226861,Human_RBP_ID_406436,Human_RBP_ID_750068,Human_RBP_ID_808715,Human_RBP_ID_1163894,Human_RBP_ID_2292118,Human_RBP_ID_3941192,Human_RBP_ID_4195505,Human_RBP_ID_5416459,Human_RBP_ID_5437044,Human_RBP_ID_5460986,Human_RBP_ID_5490562,Human_RBP_ID_6105978,Human_RBP_ID_8062779,Human_RBP_ID_8361609,Human_RBP_ID_8772653,Human_RBP_ID_9414339,Human_RBP_ID_11750298,Human_RBP_ID_18416646,Human_RBP_ID_18932875,Human_RBP_ID_22894700,Human_RBP_ID_23113143,Human_RBP_ID_23124916,Human_RBP_ID_23527532,Human_RBP_ID_24542991,Human_RBP_ID_26320549,Human_RBP_ID_26407893 Human_miRNA_ID_2428899,Human_miRNA_ID_2488700 RMVar_hsa_circ_93535,RMVar_hsa_circ_152485 86653 RMVar_ID_86653 Human_SNP_ID_477324884 m1A Human chr11 - 93741431 93741431 93741431 TGGTTATCGGGAGTTGGAGGGCTGAGGTCGGGAGGGTGGTGTGTACAGAGCTCTAGGACACCAGG TGGTTATCGGGAGTTGGAGGGCTGAGGTCGGGCGGGTGGTGTGTACAGAGCTCTAGGACACCAGG T G TAF1D Ensembl:ENSG00000166012 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr11:93741301..93741475;chr11:93741331..93741467 26863196 MeRIP-seq:(Medium) rs571146220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226861,Human_RBP_ID_406436,Human_RBP_ID_750068,Human_RBP_ID_808715,Human_RBP_ID_1163894,Human_RBP_ID_2292118,Human_RBP_ID_3941192,Human_RBP_ID_4195505,Human_RBP_ID_5416459,Human_RBP_ID_5437044,Human_RBP_ID_5460986,Human_RBP_ID_5490562,Human_RBP_ID_6105978,Human_RBP_ID_8062779,Human_RBP_ID_8361609,Human_RBP_ID_8772653,Human_RBP_ID_9414339,Human_RBP_ID_11750298,Human_RBP_ID_18416646,Human_RBP_ID_18932875,Human_RBP_ID_22894700,Human_RBP_ID_23113143,Human_RBP_ID_23124916,Human_RBP_ID_23527532,Human_RBP_ID_24542991,Human_RBP_ID_26320549,Human_RBP_ID_26407893 Human_miRNA_ID_2428899,Human_miRNA_ID_2488700 RMVar_hsa_circ_93535,RMVar_hsa_circ_152485 86654 RMVar_ID_86654 Human_SNP_ID_477324889 m1A Human chr11 + 93741436 93741436 93741436 TGTCCTAGAGCTCTGTACACACCACCCTCCCGACCTCAGCCCTCCAACTCCCGATAACCAGCCGA TGTCCTAGAGCTCTGTACACACCACCCTCCCGCCCTCAGCCCTCCAACTCCCGATAACCAGCCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:93739276..93741500;chr11:93741197..93741475;chr11:93741208..93741500;chr11:93739251..93741500;chr11:93741259..93741500 26863196 MeRIP-seq:(Medium) rs1490640135 Functional Loss SNV dbSNP153 33..33 33 - - - 86655 RMVar_ID_86655 Human_SNP_ID_477335949 m1A Human chr11 - 93784670 93784670 93784670 GGTCCCCGCCGCCTCCTCCTCCTCGGAGCCCGAACCCTGGCTGAAGTCTATCCGCTGGGCCAGAC GGTCCCCGCCGCCTCCTCCTCCTCGGAGCCCGGACCCTGGCTGAAGTCTATCCGCTGGGCCAGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:93784568..93788025 26863196 MeRIP-seq:(Medium) rs1290391031 Functional Loss SNV dbSNP153 33..33 33 - - - 86656 RMVar_ID_86656 Human_SNP_ID_477420804 m1A Human chr11 + 94128945 94128945 94128945 CCGCTTCGGCAGCCAGGGCGGCGCGGAGGGGCAGGGCCAGAGGGAAGCGCTTTGTTCCGCGCGTG CCGCTTCGGCAGCCAGGGCGGCGCGGAGGGGCCGGGCCAGAGGGAAGCGCTTTGTTCCGCGCGTG A C PANX1 Ensembl:ENSG00000110218 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:94128897..94129030 26863196 MeRIP-seq:(Medium) rs1249351852 Functional Loss SNV dbSNP153 33..33 33 - - - 86657 RMVar_ID_86657 Human_SNP_ID_477583117 m1A Human chr11 - 94768438 94768438 94768438 GGCTGCCGGGCAGCGCGGGGAAGTGGCGCCGGACAATCAACCCCATTCACACAGGGCTTCACCTC GGCTGCCGGGCAGCGCGGGGAAGTGGCGCCGGGCAATCAACCCCATTCACACAGGGCTTCACCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:94768394..94768492 26863196 MeRIP-seq:(Medium) rs1427951633 Functional Loss SNV dbSNP153 33..33 33 - - - 86658 RMVar_ID_86658 Human_SNP_ID_477583140 m1A Human chr11 - 94768475 94768475 94768475 CGATCATGGCTAGTTCAGTCCCTCGGCTGGGGAAGACGGCTGCCGGGCAGCGCGGGGAAGTGGCG CGATCATGGCTAGTTCAGTCCCTCGGCTGGGGGAGACGGCTGCCGGGCAGCGCGGGGAAGTGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:94768426..94768497 26863196 MeRIP-seq:(Medium) rs901087983 Functional Loss SNV dbSNP153 33..33 33 - - - 86659 RMVar_ID_86659 Human_SNP_ID_477590219 m1A Human chr11 + 94799751 94799751 94799751 CGGTCCACGCAGCCTCAGCAGAACAACGAGGAACTGCCCACTTACGAGGAGGCCAAAGCACAGTC CGGTCCACGCAGCCTCAGCAGAACAACGAGGAGCTGCCCACTTACGAGGAGGCCAAAGCACAGTC A G AMOTL1 Ensembl:ENSG00000166025 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:94799705..94799790 26863196 MeRIP-seq:(Medium) rs1242932692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8772763,Human_RBP_ID_17803641,Human_RBP_ID_18614826,Human_RBP_ID_26319137 RMVar_hsa_circ_937,RMVar_hsa_circ_23931,RMVar_hsa_circ_296682,RMVar_hsa_circ_324823,RMVar_hsa_circ_269958,RMVar_hsa_circ_152553,RMVar_hsa_circ_152554,RMVar_hsa_circ_274662,RMVar_hsa_circ_345633,RMVar_hsa_circ_51902,RMVar_hsa_circ_152555,RMVar_hsa_circ_152556 86660 RMVar_ID_86660 Human_SNP_ID_477590619 m1A Human chr11 + 94801200 94801200 94801200 TGACATTTGAGTTGGAACTTGAAGGATAAATCAGAGTTGTAGGGTAGAGATGAAGTAGCAGTATG TGACATTTGAGTTGGAACTTGAAGGATAAATCGGAGTTGTAGGGTAGAGATGAAGTAGCAGTATG A G AMOTL1 Ensembl:ENSG00000166025 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:94801194..94801485 26863196 MeRIP-seq:(Medium) rs1164944440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11753984,Human_RBP_ID_22570072 RMVar_hsa_circ_937,RMVar_hsa_circ_23931,RMVar_hsa_circ_296682,RMVar_hsa_circ_324823,RMVar_hsa_circ_152553,RMVar_hsa_circ_345633,RMVar_hsa_circ_51902,RMVar_hsa_circ_152556 86661 RMVar_ID_86661 Human_SNP_ID_477630078 m1A Human chr11 - 94970013 94970009 94970013 CTTCTTGCAGAACTGGAAAAAATTAAAAAAGAAAGAGCTGAAGAGCAGGCCAGGAAGGTAAAACC CTTCTTGCAGAACTGGAAAAAATTAAAAAAGA____GCTGAAGAGCAGGCCAGGAAGGTAAAACC CTCTT C CWC15 Ensembl:ENSG00000150316 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:94963310..94970109 32194978 MeRIP-seq:(Medium) rs1565414192 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_808930,Human_RBP_ID_988921,Human_RBP_ID_1462044,Human_RBP_ID_5342959,Human_RBP_ID_6107449,Human_RBP_ID_9362868,Human_RBP_ID_17466697,Human_RBP_ID_22643818,Human_RBP_ID_26319146,Human_RBP_ID_27805009 Human_Splice_Rec_1289260,Human_Splice_Rec_1289261,Human_Splice_Rec_1289265,Human_Splice_Rec_1289274,Human_Splice_Rec_1289275 RMVar_hsa_circ_69852,RMVar_hsa_circ_121401,RMVar_hsa_circ_152566 86662 RMVar_ID_86662 Human_SNP_ID_477630634 m1A Human chr11 - 94972121 94972121 94972121 TGCCAGAGGTGGAAGGGGAAAAGGAGAAGGTGATTTGAGCCAACTTTCAAAGCAGTATTCAAGCA TGCCAGAGGTGGAAGGGGAAAAGGAGAAGGTGGTTTGAGCCAACTTTCAAAGCAGTATTCAAGCA T C CWC15 Ensembl:ENSG00000150316 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:94971374..94972200 32194978 MeRIP-seq:(Medium) rs782246259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4183035,Human_RBP_ID_6107456,Human_RBP_ID_22034892,Human_RBP_ID_23528128,Human_RBP_ID_27805012 Human_Splice_Rec_1289254,Human_Splice_Rec_1289255,Human_Splice_Rec_1289270,Human_Splice_Rec_1289271,Human_Splice_Rec_1289280,Human_Splice_Rec_1289281,Human_Splice_Rec_1289286,Human_Splice_Rec_1289287,Human_Splice_Rec_1289292,Human_Splice_Rec_1289293 RMVar_hsa_circ_58097,RMVar_hsa_circ_69852,RMVar_hsa_circ_121401,RMVar_hsa_circ_152566 86663 RMVar_ID_86663 Human_SNP_ID_477631067 m1A Human chr11 - 94973514 94973514 94973514 ATGGCGTCTGTATGATCTTCGGAGCCTGCTGCATCGGACCTCGGCCAGTGTGAGCGGCAAGAGGA ATGGCGTCTGTATGATCTTCGGAGCCTGCTGCGTCGGACCTCGGCCAGTGTGAGCGGCAAGAGGA T C CWC15 Ensembl:ENSG00000150316 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:94972101..94973575 26863196 MeRIP-seq:(Medium) rs1555096580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_988925,Human_RBP_ID_1461598,Human_RBP_ID_1784228,Human_RBP_ID_3383196,Human_RBP_ID_4185338,Human_RBP_ID_5490577,Human_RBP_ID_6107465,Human_RBP_ID_8361928,Human_RBP_ID_8772950,Human_RBP_ID_11754981,Human_RBP_ID_18614922,Human_RBP_ID_22491997,Human_RBP_ID_23528130,Human_RBP_ID_26319148,Human_RBP_ID_27803952 Human_Splice_Rec_1289253,Human_Splice_Rec_1289269,Human_Splice_Rec_1289279 RMVar_hsa_circ_121401,RMVar_hsa_circ_152566 86664 RMVar_ID_86664 Human_SNP_ID_477631068 m1A Human chr11 + 94973517 94973517 94973517 TCTTGCCGCTCACACTGGCCGAGGTCCGATGCAGCAGGCTCCGAAGATCATACAGACGCCATTAC TCTTGCCGCTCACACTGGCCGAGGTCCGATGCGGCAGGCTCCGAAGATCATACAGACGCCATTAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:94972187..94973575 26863196 MeRIP-seq:(Medium) rs1191485863 Functional Loss SNV dbSNP153 33..33 33 - - - 86665 RMVar_ID_86665 Human_SNP_ID_477631077 m1A Human chr11 + 94973529 94973529 94973529 CACTGGCCGAGGTCCGATGCAGCAGGCTCCGAAGATCATACAGACGCCATTACCACTCTTGGCTC CACTGGCCGAGGTCCGATGCAGCAGGCTCCGACGATCATACAGACGCCATTACCACTCTTGGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:94973380..94973533 26863196 MeRIP-seq:(Medium) rs1303692095 Functional Loss SNV dbSNP153 33..33 33 - - - 86666 RMVar_ID_86666 Human_SNP_ID_477653265 m1A Human chr11 - 95067095 95067095 95067095 CGGGAAAGGCCGGGCGGAGAGGCGGGCGGCGGAGCTCCGCAGGGAGCGCCCTGGAGCAGCAACTT CGGGAAAGGCCGGGCGGAGAGGCGGGCGGCGGTGCTCCGCAGGGAGCGCCCTGGAGCAGCAACTT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95067052..95067119 26863196 MeRIP-seq:(Medium) rs1425596936 Functional Loss SNV dbSNP153 33..33 33 - - - 86667 RMVar_ID_86667 Human_SNP_ID_477691615 m1A Human chr11 + 95231038 95231038 95231038 CTGCCTGAAAGCTAGCGGCACTGCCAGAGGCGACCACCGCGGCAGCTGCCCCAGCGACGGCGGAG CTGCCTGAAAGCTAGCGGCACTGCCAGAGGCGGCCACCGCGGCAGCTGCCCCAGCGACGGCGGAG A G AP000787.1 Ensembl:ENSG00000245552 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:95230987..95231089 26863196 MeRIP-seq:(Medium) rs1290306929 Functional Loss SNV dbSNP153 33..33 33 - - - 86668 RMVar_ID_86668 Human_SNP_ID_477826923 m1A Human chr11 + 95789308 95789308 95789308 CAGACTCCCAAACCCCTGAGGCGCCGGCGAAGAGGGGCTGCAGTGCAGCGGCTACCCGGCCCCCT CAGACTCCCAAACCCCTGAGGCGCCGGCGAAGTGGGGCTGCAGTGCAGCGGCTACCCGGCCCCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95789300..95789377 26863196 MeRIP-seq:(Medium) rs1322776115 Functional Loss SNV dbSNP153 33..33 33 - - - 86669 RMVar_ID_86669 Human_SNP_ID_477827132 m1A Human chr11 + 95789621 95789621 95789621 CTGCCTCGCGCCCACCAGGGCCTCGCCGCGAGAGCCCAGGGCCCCGCGGACGACGCCACCGTCTC CTGCCTCGCGCCCACCAGGGCCTCGCCGCGAGCGCCCAGGGCCCCGCGGACGACGCCACCGTCTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:95789591..95789717 26863196 MeRIP-seq:(Medium) rs1370046616 Functional Loss SNV dbSNP153 33..33 33 - - - 86670 RMVar_ID_86670 Human_SNP_ID_477827133 m1A Human chr11 + 95789621 95789621 95789621 CTGCCTCGCGCCCACCAGGGCCTCGCCGCGAGAGCCCAGGGCCCCGCGGACGACGCCACCGTCTC CTGCCTCGCGCCCACCAGGGCCTCGCCGCGAGGGCCCAGGGCCCCGCGGACGACGCCACCGTCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:95789591..95789717 26863196 MeRIP-seq:(Medium) rs1370046616 Functional Loss SNV dbSNP153 33..33 33 - - - 86671 RMVar_ID_86671 Human_SNP_ID_477827205 m1A Human chr11 - 95789747 95789747 95789747 TCCACGGCCGCACAGCTAAACAGCAACCCCCTACCCGCTTCGTCTCCCTCCGCCGCTATCGGGGC TCCACGGCCGCACAGCTAAACAGCAACCCCCTCCCCGCTTCGTCTCCCTCCGCCGCTATCGGGGC T G FAM76B Ensembl:ENSG00000077458 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:95789547..95789784 26863196 MeRIP-seq:(Medium) rs1052459199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1289555 86672 RMVar_ID_86672 Human_SNP_ID_477827212 m1A Human chr11 - 95789754 95789753 95789754 AAGCGGATCCACGGCCGCACAGCTAAACAGCAACCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA AAGCGGATCCACGGCCGCACAGCTAAACAGCA_CCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA GT G FAM76B Ensembl:ENSG00000077458 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95789493..95789787 26863196 MeRIP-seq:(Medium) rs1464158278 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1289555 86673 RMVar_ID_86673 Human_SNP_ID_477827213 m1A Human chr11 - 95789754 95789754 95789754 AAGCGGATCCACGGCCGCACAGCTAAACAGCAACCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA AAGCGGATCCACGGCCGCACAGCTAAACAGCAGCCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA T C FAM76B Ensembl:ENSG00000077458 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95789493..95789787 26863196 MeRIP-seq:(Medium) rs890615498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1289555 86674 RMVar_ID_86674 Human_SNP_ID_477827214 m1A Human chr11 - 95789754 95789754 95789754 AAGCGGATCCACGGCCGCACAGCTAAACAGCAACCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA AAGCGGATCCACGGCCGCACAGCTAAACAGCACCCCCCTACCCGCTTCGTCTCCCTCCGCCGCTA T G FAM76B Ensembl:ENSG00000077458 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95789493..95789787 26863196 MeRIP-seq:(Medium) rs890615498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1289555 86675 RMVar_ID_86675 Human_SNP_ID_477827218 m1A Human chr11 - 95789758 95789758 95789758 AAGGAAGCGGATCCACGGCCGCACAGCTAAACAGCAACCCCCTACCCGCTTCGTCTCCCTCCGCC AAGGAAGCGGATCCACGGCCGCACAGCTAAACGGCAACCCCCTACCCGCTTCGTCTCCCTCCGCC T C FAM76B Ensembl:ENSG00000077458 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:95789170..95790159 26863196 MeRIP-seq:(Medium) rs367633419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1289555 86676 RMVar_ID_86676 Human_SNP_ID_477827495 m1A Human chr11 + 95790343 95790343 95790343 GGAGGAGGCCCGACCCTCCGTAGAATCCCCGCAGAGCCGGCCTGTAACCCCGGCGTTGTCTGCCC GGAGGAGGCCCGACCCTCCGTAGAATCCCCGCCGAGCCGGCCTGTAACCCCGGCGTTGTCTGCCC A C CEP57 Ensembl:ENSG00000166037 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95790223..95790361 26863196 MeRIP-seq:(Medium) rs1249211083 Functional Loss SNV dbSNP153 33..33 33 - - - 86677 RMVar_ID_86677 Human_SNP_ID_477828082 m1A Human chr11 - 95791814 95791814 95791814 ATCTCAAGTTTCCTAAAAGCACCTACTGTTCTAGCACATACTCCAAAATTCCCGCACTGCCTTTT ATCTCAAGTTTCCTAAAAGCACCTACTGTTCTGGCACATACTCCAAAATTCCCGCACTGCCTTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95791812..95791962 26863196 MeRIP-seq:(Medium) rs1277686517 Functional Loss SNV dbSNP153 33..33 33 - - - 86678 RMVar_ID_86678 Human_SNP_ID_477853704 m1A Human chr11 - 95892765 95892765 95892765 AAAACATTCAGATAAAGATTAGGAAGAGAATTAGTAGTTGAAGAAAGGCTTGGACAGAGAAAAGT AAAACATTCAGATAAAGATTAGGAAGAGAATTCGTAGTTGAAGAAAGGCTTGGACAGAGAAAAGT T G MTMR2 Ensembl:ENSG00000087053 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:95892762..95892861 26863196 MeRIP-seq:(Medium) rs1281650521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2293195 RMVar_hsa_circ_84825,RMVar_hsa_circ_152599,RMVar_hsa_circ_6139,RMVar_hsa_circ_331293,RMVar_hsa_circ_45953,RMVar_hsa_circ_152603,RMVar_hsa_circ_311418,RMVar_hsa_circ_311787,RMVar_hsa_circ_152604 86679 RMVar_ID_86679 Human_SNP_ID_477855860 m1A Human chr11 + 95902977 95902977 95902977 CACTCTCTCTCACTCCTTAAGACTTTAGCTTCAGGCTTACCATAATTCTTTCCAGTGCTGCCAAC CACTCTCTCTCACTCCTTAAGACTTTAGCTTCGGGCTTACCATAATTCTTTCCAGTGCTGCCAAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:95902973..95903096 26863196 MeRIP-seq:(Medium) rs1565382382 Functional Loss SNV dbSNP153 33..33 33 - - - 86680 RMVar_ID_86680 Human_SNP_ID_477860702 m1A Human chr11 + 95924003 95924003 95924003 CACAGGGAAAGGCTGAAGCAGTCTTCGCGGCTACAGGGCGGGAGAAGCGGAGGGCGGAGTGCTAC CACAGGGAAAGGCTGAAGCAGTCTTCGCGGCTGCAGGGCGGGAGAAGCGGAGGGCGGAGTGCTAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr11:95923953..95924089;chr11:95923876..95924100 26863196,26863410 MeRIP-seq:(Medium) rs1180826611 Functional Loss SNV dbSNP153 33..33 33 - - - 86681 RMVar_ID_86681 Human_SNP_ID_477916152 m1A Human chr11 + 96150771 96150771 96150771 CTGTGGTCACTACTCTAGTTCAGACCTGCTTTACCCTTGTAGGGCCACCATACTAACCCCTGCTT CTGTGGTCACTACTCTAGTTCAGACCTGCTTTCCCCTTGTAGGGCCACCATACTAACCCCTGCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:96150725..96150808 26863196 MeRIP-seq:(Medium) rs897274061 Functional Loss SNV dbSNP153 33..33 33 - - - 86682 RMVar_ID_86682 Human_SNP_ID_477973957 m1A Human chr11 - 96390075 96390075 96390075 AGTCCCTCAAAACCCGCCAGGCCCCTCTCCCCACCTCTCTTGCAACCAGGACCCGCACAGCTCCC AGTCCCTCAAAACCCGCCAGGCCCCTCTCCCCGCCTCTCTTGCAACCAGGACCCGCACAGCTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:96390028..96390646;chr11:96390032..96390735 26863196 MeRIP-seq:(Medium) rs937570688 Functional Loss SNV dbSNP153 33..33 33 - - - 86683 RMVar_ID_86683 Human_SNP_ID_222766843 m1A Human chr5 - 15928232 15928232 15928232 GGTCCACGTTGATGGTCTCGCCCGTCAGGCGGATAGTCCTCCAGAGCCGCGGGTCCCAGGCCAGG GGTCCACGTTGATGGTCTCGCCCGTCAGGCGGGTAGTCCTCCAGAGCCGCGGGTCCCAGGCCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:15928181..15928388 32194978 MeRIP-seq:(Medium) rs1332522562 Functional Loss SNV dbSNP153 33..33 33 - - - 86684 RMVar_ID_86684 Human_SNP_ID_222769076 m1A Human chr5 + 15936855 15936855 15936855 GGCCAAGTACTGCAGCAAGCTGCGCTACCTCAACGCGAGGGGCTGCGAGGGCATCACGGACCACG GGCCAAGTACTGCAGCAAGCTGCGCTACCTCAGCGCGAGGGGCTGCGAGGGCATCACGGACCACG A G FBXL7 Ensembl:ENSG00000183580 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:15936724..15936972 32194978 MeRIP-seq:(Medium) rs779828817 Functional Loss SNV dbSNP153 33..33 33 - - - 86685 RMVar_ID_86685 Human_SNP_ID_222892743 m1A Human chr5 - 16463643 16463643 16463643 GGAGCAGGATGCAGAGGAGGAAGAGGCTGAGGAAGGCCCACCCCTTGGTGCCATCCCTATCACGG GGAGCAGGATGCAGAGGAGGAAGAGGCTGAGGGAGGCCCACCCCTTGGTGCCATCCCTATCACGG T C ZNF622 Ensembl:ENSG00000173545 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:16463594..16465692 32194978 MeRIP-seq:(Medium) rs887640400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9306398 Human_Splice_Rec_636816 RMVar_hsa_circ_116922,RMVar_hsa_circ_230492 86686 RMVar_ID_86686 Human_SNP_ID_222893071 m1A Human chr5 - 16465074 16465074 16465074 CGAAGAAGTTGGCAAAGCAGCAGGAGGAGGACAGCGAGGAGGAGGAAGAGGACCTGGATGGAGAC CGAAGAAGTTGGCAAAGCAGCAGGAGGAGGACGGCGAGGAGGAGGAAGAGGACCTGGATGGAGAC T C ZNF622 Ensembl:ENSG00000173545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16463626..16465209 26863196 MeRIP-seq:(Medium) rs781425778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76839,Human_RBP_ID_840027,Human_RBP_ID_9306399,Human_RBP_ID_9397678,Human_RBP_ID_26350685,Human_RBP_ID_27826245 Human_Splice_Rec_636815 Human_miRNA_ID_2570268 RMVar_hsa_circ_116922,RMVar_hsa_circ_230492 86687 RMVar_ID_86687 Human_SNP_ID_222893077 m1A Human chr5 - 16465085 16465085 16465085 TGAACAGCAGGCGAAGAAGTTGGCAAAGCAGCAGGAGGAGGACAGCGAGGAGGAGGAAGAGGACC TGAACAGCAGGCGAAGAAGTTGGCAAAGCAGCGGGAGGAGGACAGCGAGGAGGAGGAAGAGGACC T C ZNF622 Ensembl:ENSG00000173545 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:16463526..16465800;chr5:16463551..16465800 26863196 MeRIP-seq:(Medium) rs748058936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76839,Human_RBP_ID_840027,Human_RBP_ID_9306399,Human_RBP_ID_9397678,Human_RBP_ID_27826245 Human_Splice_Rec_636815 Human_miRNA_ID_2511155,Human_miRNA_ID_3053978 RMVar_hsa_circ_116922,RMVar_hsa_circ_230492 86688 RMVar_ID_86688 Human_SNP_ID_222893179 m1A Human chr5 - 16465353 16465353 16465353 TGGAGAAGAAGGCCGTGCAGGCAGTGAATCGGAAAGTGGAGATGATGAATGAAAAGAACTTGGAG TGGAGAAGAAGGCCGTGCAGGCAGTGAATCGGCAAGTGGAGATGATGAATGAAAAGAACTTGGAG T G ZNF622 Ensembl:ENSG00000173545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16465303..16465800 26863196 MeRIP-seq:(Medium) rs1488059626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76841,Human_RBP_ID_1649499,Human_RBP_ID_4820980,Human_RBP_ID_24094461 RMVar_hsa_circ_116922,RMVar_hsa_circ_230492 86689 RMVar_ID_86689 Human_SNP_ID_222908009 m1A Human chr5 + 16528521 16528521 16528521 CAGCTCTGGATGACATGGAGGCCAGTCTCTTCAGGAGCAAAAGAAAGATTAGGGGGCCAAGGAGG CAGCTCTGGATGACATGGAGGCCAGTCTCTTCGGGAGCAAAAGAAAGATTAGGGGGCCAAGGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16528516..16528593 26863196 MeRIP-seq:(Medium) rs1179155614 Functional Loss SNV dbSNP153 33..33 33 - - - 86690 RMVar_ID_86690 Human_SNP_ID_222908010 m1A Human chr5 + 16528521 16528521 16528521 CAGCTCTGGATGACATGGAGGCCAGTCTCTTCAGGAGCAAAAGAAAGATTAGGGGGCCAAGGAGG CAGCTCTGGATGACATGGAGGCCAGTCTCTTCTGGAGCAAAAGAAAGATTAGGGGGCCAAGGAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16528516..16528593 26863196 MeRIP-seq:(Medium) rs1179155614 Functional Loss SNV dbSNP153 33..33 33 - - - 86691 RMVar_ID_86691 Human_SNP_ID_222908024 m1A Human chr5 - 16528537 16528537 16528537 TGGGACAGGTCTCACTCCTCCTTGGCCCCCTAATCTTTCTTTTGCTCCTGAAGAGACTGGCCTCC TGGGACAGGTCTCACTCCTCCTTGGCCCCCTAGTCTTTCTTTTGCTCCTGAAGAGACTGGCCTCC T C RETREG1 Ensembl:ENSG00000154153 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16528530..16528639 26863196 MeRIP-seq:(Medium) rs769754671 Functional Loss SNV dbSNP153 33..33 33 - - - 86692 RMVar_ID_86692 Human_SNP_ID_222923812 m1A Human chr5 + 16598090 16598090 16598090 CCTTCCATCTCCCCACCTCCCGACCACACGGAACTCTGTGCACATTTTTGGCAGTCCACACTCCT CCTTCCATCTCCCCACCTCCCGACCACACGGAGCTCTGTGCACATTTTTGGCAGTCCACACTCCT A G RF00017-4498 RNACentral:URS0000923951 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16598085..16598167 26863196 MeRIP-seq:(Medium) rs568121279 Functional Loss SNV dbSNP153 33..33 33 - - - 86693 RMVar_ID_86693 Human_SNP_ID_222928204 m1A Human chr5 - 16616949 16616949 16616949 ACAGCTGAAGATGGCGAGCCCGGCGCCTCCGGAGCACGCCGAGGAGGGATGCCCGGCTCCTGCCG ACAGCTGAAGATGGCGAGCCCGGCGCCTCCGGGGCACGCCGAGGAGGGATGCCCGGCTCCTGCCG T C RETREG1 Ensembl:ENSG00000154153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16616708..16617073 26863196 MeRIP-seq:(Medium) rs571527296 Functional Loss SNV dbSNP153 33..33 33 - - - 86694 RMVar_ID_86694 Human_SNP_ID_222928209 m1A Human chr5 + 16616954 16616952 16616954 GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGAGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC GGAGCCGGGCATCCCTCCTCGGCGTGCTCCG__GGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC GGA G AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:16616698..16617104;chr5:16616660..16617058 26863196 MeRIP-seq:(Medium) rs137852736 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_468 86695 RMVar_ID_86695 Human_SNP_ID_222928214 m1A Human chr5 + 16616954 16616954 16616954 GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGAGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGCGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC A C AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:16616698..16617104;chr5:16616660..16617058 26863196 MeRIP-seq:(Medium) rs773314283 Functional Loss SNV dbSNP153 33..33 33 - - - 86696 RMVar_ID_86696 Human_SNP_ID_222928215 m1A Human chr5 + 16616954 16616954 16616954 GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGAGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGGGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC A G AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:16616698..16617104;chr5:16616660..16617058 26863196 MeRIP-seq:(Medium) rs773314283 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 86697 RMVar_ID_86697 Human_SNP_ID_222942929 m1A Human chr5 + 16666101 16666101 16666101 AAAGTGTTGAGTTTATGAACACATGCACGAACAGGCAAGCACGTACACTTAAAAGATGAAACAAA AAAGTGTTGAGTTTATGAACACATGCACGAACGGGCAAGCACGTACACTTAAAAGATGAAACAAA A G AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:16666052..16666152 32194978 MeRIP-seq:(Medium) rs1384881389 Functional Loss SNV dbSNP153 33..33 33 - - - 86698 RMVar_ID_86698 Human_SNP_ID_222943034 m1A Human chr5 - 16666450 16666450 16666450 GTTTCCAAAGCTTTACTACTCTTAGAGGACACATGCCTTAAAAAAGGAGGGGAGGAACCACGCTG GTTTCCAAAGCTTTACTACTCTTAGAGGACACGTGCCTTAAAAAAGGAGGGGAGGAACCACGCTG T C MYO10 Ensembl:ENSG00000145555 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:16666401..16666551 32194978 MeRIP-seq:(Medium) rs1289257524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4821092 Human_miRNA_ID_1062334 86699 RMVar_ID_86699 Human_SNP_ID_222945392 m1A Human chr5 + 16673733 16673733 16673733 GAGTTGATGGTGATCTTGCAGGAGCCGCCGCCATGGCAATAGACCGTGGATGTCATTTCCTGCCT GAGTTGATGGTGATCTTGCAGGAGCCGCCGCCGTGGCAATAGACCGTGGATGTCATTTCCTGCCT A G AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16673701..16673775 26863196 MeRIP-seq:(Medium) rs1485232516 Functional Loss SNV dbSNP153 33..33 33 - - - 86700 RMVar_ID_86700 Human_SNP_ID_222945395 m1A Human chr5 - 16673740 16673740 16673740 GATCCACAGGCAGGAAATGACATCCACGGTCTATTGCCATGGCGGCGGCTCCTGCAAGATCACCA GATCCACAGGCAGGAAATGACATCCACGGTCTTTTGCCATGGCGGCGGCTCCTGCAAGATCACCA T A MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16673650..16673781 26863196 MeRIP-seq:(Medium) rs745877715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75534,Human_RBP_ID_4821124,Human_RBP_ID_8887649,Human_RBP_ID_9397681,Human_RBP_ID_27513558 Human_Splice_Rec_636953,Human_Splice_Rec_637033,Human_Splice_Rec_637075,Human_Splice_Rec_637117 Human_miRNA_ID_3010331 RMVar_hsa_circ_20763,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_29157,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230497,RMVar_hsa_circ_230494,RMVar_hsa_circ_266937,RMVar_hsa_circ_230498 86701 RMVar_ID_86701 Human_SNP_ID_222945396 m1A Human chr5 - 16673740 16673740 16673740 GATCCACAGGCAGGAAATGACATCCACGGTCTATTGCCATGGCGGCGGCTCCTGCAAGATCACCA GATCCACAGGCAGGAAATGACATCCACGGTCTGTTGCCATGGCGGCGGCTCCTGCAAGATCACCA T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16673650..16673781 26863196 MeRIP-seq:(Medium) rs745877715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75534,Human_RBP_ID_4821124,Human_RBP_ID_8887649,Human_RBP_ID_9397681,Human_RBP_ID_27513558 Human_Splice_Rec_636953,Human_Splice_Rec_637033,Human_Splice_Rec_637075,Human_Splice_Rec_637117 Human_miRNA_ID_3010331 RMVar_hsa_circ_20763,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_29157,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230497,RMVar_hsa_circ_230494,RMVar_hsa_circ_266937,RMVar_hsa_circ_230498 86702 RMVar_ID_86702 Human_SNP_ID_222945867 m1A Human chr5 - 16675120 16675120 16675120 AGTGCTCAAAGACAAAGGCTATACCACCCTTCAGGATGAGGCCATCAAGATATTCAATTCCCTGC AGTGCTCAAAGACAAAGGCTATACCACCCTTCGGGATGAGGCCATCAAGATATTCAATTCCCTGC T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16675069..16675186 26863196 MeRIP-seq:(Medium) rs746155942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75536,Human_RBP_ID_9398974 Human_Splice_Rec_636950,Human_Splice_Rec_637030,Human_Splice_Rec_637072,Human_Splice_Rec_637114 RMVar_hsa_circ_20763,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_29157,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230497,RMVar_hsa_circ_230494,RMVar_hsa_circ_266937,RMVar_hsa_circ_24729,RMVar_hsa_circ_230498 86703 RMVar_ID_86703 Human_SNP_ID_222945879 m1A Human chr5 - 16675152 16675152 16675152 CAGATGAGTTCCGTGTTTGTTTTGCTTGTCCTAGTGCTCAAAGACAAAGGCTATACCACCCTTCA CAGATGAGTTCCGTGTTTGTTTTGCTTGTCCTGGTGCTCAAAGACAAAGGCTATACCACCCTTCA T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16675126..16675175 26863196 MeRIP-seq:(Medium) rs1345708723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75536 RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_29157,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230497,RMVar_hsa_circ_230494,RMVar_hsa_circ_266937,RMVar_hsa_circ_24729,RMVar_hsa_circ_230498 86704 RMVar_ID_86704 Human_SNP_ID_222946092 m1A Human chr5 - 16676028 16676028 16676028 CCCTTCCGTATGGGGACATAAATCTCAACTGTAAGTCCAGAGCTCCACCCCGACTCCTCAGAGAC CCCTTCCGTATGGGGACATAAATCTCAACTGTGAGTCCAGAGCTCCACCCCGACTCCTCAGAGAC T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16676026..16676075 26863196 MeRIP-seq:(Medium) rs1471968460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124349 RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_29157,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230497,RMVar_hsa_circ_230494,RMVar_hsa_circ_266937,RMVar_hsa_circ_24729,RMVar_hsa_circ_230498 86705 RMVar_ID_86705 Human_SNP_ID_222953241 m1A Human chr5 - 16701364 16701364 16701364 ACGACGACGCCTTCAAGGACTCCCCCAACCCCAGCGAGCACGGCCACTCAGACCAGCGAACAAGT ACGACGACGCCTTCAAGGACTCCCCCAACCCCCGCGAGCACGGCCACTCAGACCAGCGAACAAGT T G MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:16701218..16701368 32194978 MeRIP-seq:(Medium) rs766304667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75551,Human_RBP_ID_4821184,Human_RBP_ID_8887678 Human_miRNA_ID_2683547 RMVar_hsa_circ_42338,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230498,RMVar_hsa_circ_264947,RMVar_hsa_circ_230499,RMVar_hsa_circ_126247,RMVar_hsa_circ_97329,RMVar_hsa_circ_107631,RMVar_hsa_circ_230501,RMVar_hsa_circ_110190,RMVar_hsa_circ_289935,RMVar_hsa_circ_230502,RMVar_hsa_circ_117125,RMVar_hsa_circ_95398,RMVar_hsa_circ_3584,RMVar_hsa_circ_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_74659,RMVar_hsa_circ_44006,RMVar_hsa_circ_120862,RMVar_hsa_circ_330089,RMVar_hsa_circ_230510 86706 RMVar_ID_86706 Human_SNP_ID_222953760 m1A Human chr5 - 16702975 16702975 16702975 CAATTGCTGGCAGAGAAAAGGGAGCAAGAAGAAAAGAAGAAACAGGAAGAGGAAGAAAAGAAGAA CAATTGCTGGCAGAGAAAAGGGAGCAAGAAGAGAAGAAGAAACAGGAAGAGGAAGAAAAGAAGAA T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:16702846..16703025 26863196 MeRIP-seq:(Medium) rs1301997006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75553,Human_RBP_ID_24548089 Human_Splice_Rec_636927,Human_Splice_Rec_637007,Human_Splice_Rec_637049,Human_Splice_Rec_637091 RMVar_hsa_circ_42338,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230498,RMVar_hsa_circ_264947,RMVar_hsa_circ_230499,RMVar_hsa_circ_126247,RMVar_hsa_circ_97329,RMVar_hsa_circ_107631,RMVar_hsa_circ_230501,RMVar_hsa_circ_110190,RMVar_hsa_circ_289935,RMVar_hsa_circ_230502,RMVar_hsa_circ_117125,RMVar_hsa_circ_95398,RMVar_hsa_circ_3584,RMVar_hsa_circ_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_74659,RMVar_hsa_circ_44006,RMVar_hsa_circ_120862,RMVar_hsa_circ_230510 86707 RMVar_ID_86707 Human_SNP_ID_222953761 m1A Human chr5 - 16702976 16702976 16702976 ACAATTGCTGGCAGAGAAAAGGGAGCAAGAAGAAAAGAAGAAACAGGAAGAGGAAGAAAAGAAGA ACAATTGCTGGCAGAGAAAAGGGAGCAAGAAGGAAAGAAGAAACAGGAAGAGGAAGAAAAGAAGA T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr5:16702871..16703090;chr5:16702868..16703125 26863196 MeRIP-seq:(Medium) rs927059709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75553,Human_RBP_ID_23042195,Human_RBP_ID_24548089 Human_Splice_Rec_636927,Human_Splice_Rec_637007,Human_Splice_Rec_637049,Human_Splice_Rec_637091 RMVar_hsa_circ_42338,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230498,RMVar_hsa_circ_264947,RMVar_hsa_circ_230499,RMVar_hsa_circ_126247,RMVar_hsa_circ_97329,RMVar_hsa_circ_107631,RMVar_hsa_circ_230501,RMVar_hsa_circ_110190,RMVar_hsa_circ_289935,RMVar_hsa_circ_230502,RMVar_hsa_circ_117125,RMVar_hsa_circ_95398,RMVar_hsa_circ_3584,RMVar_hsa_circ_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_74659,RMVar_hsa_circ_44006,RMVar_hsa_circ_120862,RMVar_hsa_circ_230510 86708 RMVar_ID_86708 Human_SNP_ID_222978769 m1A Human chr5 - 16794749 16794749 16794749 GGCTGTACGAGCCTGCCACCATGGAGCAGTACAGCCGGCGCCACCTGGGCGAGCTGCCCCCGCAC GGCTGTACGAGCCTGCCACCATGGAGCAGTACGGCCGGCGCCACCTGGGCGAGCTGCCCCCGCAC T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:16794699..16794873 26863196 MeRIP-seq:(Medium) rs928231962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_636890,Human_Splice_Rec_636968,Human_Splice_Rec_637132,Human_Splice_Rec_637200 RMVar_hsa_circ_83762,RMVar_hsa_circ_230526,RMVar_hsa_circ_126503,RMVar_hsa_circ_102206,RMVar_hsa_circ_119010,RMVar_hsa_circ_230533,RMVar_hsa_circ_314281,RMVar_hsa_circ_230538,RMVar_hsa_circ_19369,RMVar_hsa_circ_19021,RMVar_hsa_circ_230541,RMVar_hsa_circ_328441,RMVar_hsa_circ_337589,RMVar_hsa_circ_230542 86709 RMVar_ID_86709 Human_SNP_ID_222981386 m1A Human chr5 - 16804247 16804247 16804247 GGTGAGGCCCTGAGCAGACCAGGACAGCACAGATGAAGGGAGTGGGTGGGTCGCCCTGGAGTTAA GGTGAGGCCCTGAGCAGACCAGGACAGCACAGGTGAAGGGAGTGGGTGGGTCGCCCTGGAGTTAA T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16804245..16804318 26863196 MeRIP-seq:(Medium) rs1041570545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83762,RMVar_hsa_circ_230526,RMVar_hsa_circ_102206,RMVar_hsa_circ_119010,RMVar_hsa_circ_230538,RMVar_hsa_circ_230541,RMVar_hsa_circ_328441,RMVar_hsa_circ_337589,RMVar_hsa_circ_230542 86710 RMVar_ID_86710 Human_SNP_ID_222982941 m1A Human chr5 + 16810239 16810239 16810239 CCTAAAAAACACTTGTTCTCACTCTGCTCAGGAGCTTCCAGGACGGTGCCACGTTTTCACAGCCA CCTAAAAAACACTTGTTCTCACTCTGCTCAGGTGCTTCCAGGACGGTGCCACGTTTTCACAGCCA A T RF00017-4498 RNACentral:URS0000923951 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:16810236..16810448 26863196 MeRIP-seq:(Medium) rs779998057 Functional Loss SNV dbSNP153 33..33 33 - - - 86711 RMVar_ID_86711 Human_SNP_ID_222985062 m1A Human chr5 - 16818103 16818103 16818103 CCAGAAGGTGACTGCTATGCACCCCACGAACGAGGAGGGCGTGGATGACATGGCGTCCTTGACAG CCAGAAGGTGACTGCTATGCACCCCACGAACGGGGAGGGCGTGGATGACATGGCGTCCTTGACAG T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16818076..16818150 26863196 MeRIP-seq:(Medium) rs1421134308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_636888,Human_Splice_Rec_636889,Human_Splice_Rec_636966,Human_Splice_Rec_636967,Human_Splice_Rec_637130,Human_Splice_Rec_637131,Human_Splice_Rec_637198,Human_Splice_Rec_637199,Human_Splice_Rec_637210,Human_Splice_Rec_637211 RMVar_hsa_circ_83762,RMVar_hsa_circ_230526,RMVar_hsa_circ_230543,RMVar_hsa_circ_102206,RMVar_hsa_circ_119010,RMVar_hsa_circ_230538,RMVar_hsa_circ_230541,RMVar_hsa_circ_328441,RMVar_hsa_circ_337589,RMVar_hsa_circ_372634,RMVar_hsa_circ_230542,RMVar_hsa_circ_338452 86712 RMVar_ID_86712 Human_SNP_ID_222985075 m1A Human chr5 - 16818119 16818119 16818119 AGAGCACAATTACCCACCAGAAGGTGACTGCTATGCACCCCACGAACGAGGAGGGCGTGGATGAC AGAGCACAATTACCCACCAGAAGGTGACTGCTGTGCACCCCACGAACGAGGAGGGCGTGGATGAC T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16818068..16818208 26863196 MeRIP-seq:(Medium) rs1286922646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_637288,Human_RBP_ID_4821685 Human_Splice_Rec_636888,Human_Splice_Rec_636966,Human_Splice_Rec_637130,Human_Splice_Rec_637198,Human_Splice_Rec_637210 Human_miRNA_ID_2092914 RMVar_hsa_circ_83762,RMVar_hsa_circ_230526,RMVar_hsa_circ_230543,RMVar_hsa_circ_102206,RMVar_hsa_circ_119010,RMVar_hsa_circ_230538,RMVar_hsa_circ_230541,RMVar_hsa_circ_328441,RMVar_hsa_circ_337589,RMVar_hsa_circ_372634,RMVar_hsa_circ_230542,RMVar_hsa_circ_338452 86713 RMVar_ID_86713 Human_SNP_ID_223001329 m1A Human chr5 - 16877645 16877645 16877645 CAGCATTTTCCAAGTACTGTAAATTCCTGTGCAGAAGGCATCGTCGTCTTCCGGACAGACTATGG CAGCATTTTCCAAGTACTGTAAATTCCTGTGCGGAAGGCATCGTCGTCTTCCGGACAGACTATGG T C MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:16818080..16916118 32194978 MeRIP-seq:(Medium) rs771390616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75587,Human_RBP_ID_2914500,Human_RBP_ID_4821702,Human_RBP_ID_5610616,Human_RBP_ID_9174258,Human_RBP_ID_18837859 Human_Splice_Rec_636886,Human_Splice_Rec_636887,Human_Splice_Rec_636964,Human_Splice_Rec_636965,Human_Splice_Rec_637128,Human_Splice_Rec_637129,Human_Splice_Rec_637208,Human_Splice_Rec_637209 Human_miRNA_ID_2869503,Human_miRNA_ID_3057055 RMVar_hsa_circ_119010,RMVar_hsa_circ_230538,RMVar_hsa_circ_328441,RMVar_hsa_circ_230542,RMVar_hsa_circ_338452,RMVar_hsa_circ_292520 86714 RMVar_ID_86714 Human_SNP_ID_223007694 m1A Human chr5 + 16901117 16901117 16901117 CTGTGCATGATCTGGCTCCTGCCTGCCCCTCCAGCGTTGTCTCAGCCCCCCTCTCCCGAGACTCT CTGTGCATGATCTGGCTCCTGCCTGCCCCTCCGGCGTTGTCTCAGCCCCCCTCTCCCGAGACTCT A G RF00017-4498 RNACentral:URS0000923951 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:16901114..16901220 26863196 MeRIP-seq:(Medium) rs1358693979 Functional Loss SNV dbSNP153 33..33 33 - - - 86715 RMVar_ID_86715 Human_SNP_ID_223007705 m1A Human chr5 - 16901136 16901136 16901136 GCCTGGGTGAGAGCTGAGAAGAGTCTCGGGAGAGGGGGGCTGAGACAACGCTGGAGGGGCAGGCA GCCTGGGTGAGAGCTGAGAAGAGTCTCGGGAGTGGGGGGCTGAGACAACGCTGGAGGGGCAGGCA T A MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:16901130..16901341 26863196 MeRIP-seq:(Medium) rs903256189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75589 RMVar_hsa_circ_119010,RMVar_hsa_circ_230538 86716 RMVar_ID_86716 Human_SNP_ID_223007789 m1A Human chr5 - 16901511 16901511 16901511 ACGCGAAAGGTGAAGGTCATTGTTAATAGGGCAGGGCTGGTAAGAGACAAATACGCTCTTCTGGC ACGCGAAAGGTGAAGGTCATTGTTAATAGGGCGGGGCTGGTAAGAGACAAATACGCTCTTCTGGC T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:16901507..16901713 26863196 MeRIP-seq:(Medium) rs1327565333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7413982,Human_RBP_ID_15371864 RMVar_hsa_circ_119010,RMVar_hsa_circ_230538 86717 RMVar_ID_86717 Human_SNP_ID_223007790 m1A Human chr5 - 16901511 16901511 16901511 ACGCGAAAGGTGAAGGTCATTGTTAATAGGGCAGGGCTGGTAAGAGACAAATACGCTCTTCTGGC ACGCGAAAGGTGAAGGTCATTGTTAATAGGGCCGGGCTGGTAAGAGACAAATACGCTCTTCTGGC T G MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:16901507..16901713 26863196 MeRIP-seq:(Medium) rs1327565333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7413982,Human_RBP_ID_15371864 RMVar_hsa_circ_119010,RMVar_hsa_circ_230538 86718 RMVar_ID_86718 Human_SNP_ID_223072780 m1A Human chr5 - 17124920 17124907 17124921 AAGGAGAAAGGAAGGAAGGAACGAAGGAACAAAGGAAGGAAGGAAGAGGAAGGAAGGAAGGAAGA AAGGAGAAAGGAAGGAAGGAACGAAGGAACA______________GAGGAAGGAAGGAAGGAAGA CTTCCTTCCTTCCTT C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:17124912..17124977 26863196 MeRIP-seq:(Medium) rs1206133088 Functional Loss DEL dbSNP153 32..45 33 - - - 86719 RMVar_ID_86719 Human_SNP_ID_223092299 m1A Human chr5 + 17204086 17204086 17204086 CTAGCTAATGCTGCATTTCTCTGCTTCCTGTCACAATCAATAAAACTTCTGGAAAGTTTCGTCTG CTAGCTAATGCTGCATTTCTCTGCTTCCTGTCGCAATCAATAAAACTTCTGGAAAGTTTCGTCTG A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17203855..17204397 26863196 MeRIP-seq:(Medium) rs57900343 Functional Loss SNV dbSNP153 33..33 33 - - - 86720 RMVar_ID_86720 Human_SNP_ID_223093618 m1A Human chr5 - 17209013 17209013 17209013 GTCCAGACAGGCAACTTTGTGCTGGAGTTGACAGTGAGATTCTCCCTCCATGGGCTGGAGGGTGG GTCCAGACAGGCAACTTTGTGCTGGAGTTGACGGTGAGATTCTCCCTCCATGGGCTGGAGGGTGG T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:17208891..17209055 26863196 MeRIP-seq:(Medium) rs765461587 Functional Loss SNV dbSNP153 33..33 33 - - - 86721 RMVar_ID_86721 Human_SNP_ID_223095521 m1A Human chr5 + 17217085 17217085 17217085 GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGAGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGGGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17217080..17217282 26863196 MeRIP-seq:(Medium) rs1158852455 Functional Loss SNV dbSNP153 33..33 33 - - - 86722 RMVar_ID_86722 Human_SNP_ID_223095522 m1A Human chr5 + 17217085 17217085 17217085 GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGAGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGTGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT A T BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17217080..17217282 26863196 MeRIP-seq:(Medium) rs1158852455 Functional Loss SNV dbSNP153 33..33 33 - - - 86723 RMVar_ID_86723 Human_SNP_ID_223109022 m1A Human chr5 + 17275437 17275437 17275437 GGGCAAGGCCGAGGAGAAGGAGGGCGAGAAGGACGCGGCGGCTGCCAAGGAGGAGGCCCCGAAGG GGGCAAGGCCGAGGAGAAGGAGGGCGAGAAGGTCGCGGCGGCTGCCAAGGAGGAGGCCCCGAAGG A T BASP1 Ensembl:ENSG00000176788 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:17275266..17275563 26863196 MeRIP-seq:(Medium) rs964761897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4852824,Human_RBP_ID_24505350 86724 RMVar_ID_86724 Human_SNP_ID_223116960 m1A Human chr5 + 17306764 17306764 17306764 AGAAGGCCTGGGATACAACTCAGATGCAGAGCAAAAACGTGCTGAAGACCCGCCGGCAGAAGATG AGAAGGCCTGGGATACAACTCAGATGCAGAGCCAAAACGTGCTGAAGACCCGCCGGCAGAAGATG A C AC026785.1 Ensembl:ENSG00000185296 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:17306751..17306826 26863196 MeRIP-seq:(Medium) rs546044478 Functional Loss SNV dbSNP153 33..33 33 - - - 86725 RMVar_ID_86725 Human_SNP_ID_224141898 m1A Human chr5 - 21459549 21459549 21459549 CGCTGGGCCCAGAGCGCTCCATGGCTGGCCGCACGCCGCAGAACCAGCCACAGAGACAGCCCAAA CGCTGGGCCCAGAGCGCTCCATGGCTGGCCGCCCGCCGCAGAACCAGCCACAGAGACAGCCCAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:21459524..21459603;chr5:21459522..21459643 26863196 MeRIP-seq:(Medium) rs762432868 Functional Loss SNV dbSNP153 33..33 33 - - - 86726 RMVar_ID_86726 Human_SNP_ID_224141927 m1A Human chr5 + 21459582 21459582 21459582 GCGGCCAGCCATGGAGCGCTCTGGGCCCAGCGAAGGTGGGTTTCATGAAGCGAGTCCTGGCGGGG GCGGCCAGCCATGGAGCGCTCTGGGCCCAGCGCAGGTGGGTTTCATGAAGCGAGTCCTGGCGGGG A C GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:21459532..21459621 26863196 MeRIP-seq:(Medium) rs772793481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424934,Human_RBP_ID_19125389 Human_Splice_Rec_638705,Human_Splice_Rec_638709,Human_Splice_Rec_638715,Human_Splice_Rec_638723 RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 86727 RMVar_ID_86727 Human_SNP_ID_224141928 m1A Human chr5 + 21459582 21459582 21459582 GCGGCCAGCCATGGAGCGCTCTGGGCCCAGCGAAGGTGGGTTTCATGAAGCGAGTCCTGGCGGGG GCGGCCAGCCATGGAGCGCTCTGGGCCCAGCGTAGGTGGGTTTCATGAAGCGAGTCCTGGCGGGG A T GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:21459532..21459621 26863196 MeRIP-seq:(Medium) rs772793481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424934,Human_RBP_ID_19125389 Human_Splice_Rec_638705,Human_Splice_Rec_638709,Human_Splice_Rec_638715,Human_Splice_Rec_638723 RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 86728 RMVar_ID_86728 Human_SNP_ID_225729415 m1A Human chr5 + 27485375 27485375 27485375 GGAGATTTTGTTCAAAGGGGGAGCATAAGCTAAGGAATAAAGCCACAAACAATGATTAAATTAGG GGAGATTTTGTTCAAAGGGGGAGCATAAGCTAGGGAATAAAGCCACAAACAATGATTAAATTAGG A G PURPL Ensembl:ENSG00000250337 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:27485337..27485448 26863196 MeRIP-seq:(Medium) rs989102110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5615318 RMVar_hsa_circ_103994,RMVar_hsa_circ_51584,RMVar_hsa_circ_230600 86729 RMVar_ID_86729 Human_SNP_ID_297716746 m1A Human chr6 - 135316573 135316573 135316573 AAGGAAAAGGAAAAAAAGAAAAAATAATAAACAGAAAAAAGTGCCCTGGAAGCCAGAAGAGGTAG AAGGAAAAGGAAAAAAAGAAAAAATAATAAACGGAAAAAAGTGCCCTGGAAGCCAGAAGAGGTAG T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:135316524..135316613 26863196 MeRIP-seq:(Medium) rs1422033194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38246,RMVar_hsa_circ_295688,RMVar_hsa_circ_58003,RMVar_hsa_circ_291676,RMVar_hsa_circ_330785,RMVar_hsa_circ_358495,RMVar_hsa_circ_241631,RMVar_hsa_circ_339594,RMVar_hsa_circ_327263,RMVar_hsa_circ_72687,RMVar_hsa_circ_277369,RMVar_hsa_circ_70681,RMVar_hsa_circ_241633,RMVar_hsa_circ_241634,RMVar_hsa_circ_241632 86730 RMVar_ID_86730 Human_SNP_ID_297732232 m1A Human chr6 - 135379896 135379896 135379896 GGAGGGAGGAAGGAAGGAAGGAAAGGGAAGGGAGCTTGGAAAAAAGGAAGCTAGGAAGGAAGGAA GGAGGGAGGAAGGAAGGAAGGAAAGGGAAGGGGGCTTGGAAAAAAGGAAGCTAGGAAGGAAGGAA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:135379696..135379910 26863196 MeRIP-seq:(Medium) rs564808399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8215358,Human_RBP_ID_9438211,Human_RBP_ID_17069828 RMVar_hsa_circ_38246,RMVar_hsa_circ_291676,RMVar_hsa_circ_330785,RMVar_hsa_circ_327263,RMVar_hsa_circ_72687,RMVar_hsa_circ_70681,RMVar_hsa_circ_85462,RMVar_hsa_circ_11419,RMVar_hsa_circ_299373,RMVar_hsa_circ_241634,RMVar_hsa_circ_335844,RMVar_hsa_circ_95389,RMVar_hsa_circ_270586,RMVar_hsa_circ_64241,RMVar_hsa_circ_265840,RMVar_hsa_circ_241635,RMVar_hsa_circ_241636,RMVar_hsa_circ_241639,RMVar_hsa_circ_285958,RMVar_hsa_circ_279097,RMVar_hsa_circ_312581,RMVar_hsa_circ_100775,RMVar_hsa_circ_113106,RMVar_hsa_circ_95253,RMVar_hsa_circ_241641,RMVar_hsa_circ_7344,RMVar_hsa_circ_76425,RMVar_hsa_circ_84561,RMVar_hsa_circ_40036,RMVar_hsa_circ_241643,RMVar_hsa_circ_241645,RMVar_hsa_circ_241646,RMVar_hsa_circ_241647,RMVar_hsa_circ_241644,RMVar_hsa_circ_241642,RMVar_hsa_circ_241640 86731 RMVar_ID_86731 Human_SNP_ID_297732326 m1A Human chr6 - 135380088 135380088 135380088 GAGTGGTCAAGGAAAGCTTCACAAAGTAGCTGAGAATTAAGCAAAATTCAGATGACGACAAAGAA GAGTGGTCAAGGAAAGCTTCACAAAGTAGCTGTGAATTAAGCAAAATTCAGATGACGACAAAGAA T A AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:135380050..135380265 26863196 MeRIP-seq:(Medium) rs1246841472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38246,RMVar_hsa_circ_291676,RMVar_hsa_circ_330785,RMVar_hsa_circ_327263,RMVar_hsa_circ_72687,RMVar_hsa_circ_70681,RMVar_hsa_circ_85462,RMVar_hsa_circ_11419,RMVar_hsa_circ_299373,RMVar_hsa_circ_241634,RMVar_hsa_circ_335844,RMVar_hsa_circ_95389,RMVar_hsa_circ_270586,RMVar_hsa_circ_64241,RMVar_hsa_circ_265840,RMVar_hsa_circ_241635,RMVar_hsa_circ_241636,RMVar_hsa_circ_241639,RMVar_hsa_circ_285958,RMVar_hsa_circ_279097,RMVar_hsa_circ_312581,RMVar_hsa_circ_100775,RMVar_hsa_circ_113106,RMVar_hsa_circ_95253,RMVar_hsa_circ_241641,RMVar_hsa_circ_7344,RMVar_hsa_circ_76425,RMVar_hsa_circ_84561,RMVar_hsa_circ_40036,RMVar_hsa_circ_241643,RMVar_hsa_circ_241645,RMVar_hsa_circ_241646,RMVar_hsa_circ_241647,RMVar_hsa_circ_241644,RMVar_hsa_circ_241642,RMVar_hsa_circ_241640 86732 RMVar_ID_86732 Human_SNP_ID_297760866 m1A Human chr6 - 135497666 135497660 135497666 TTAGGTGGCTGCGTGGCCGCCTCACTTCGCGCACGCGCCGCTAGGCTGGGGGAGTTGATTTGCAC TTAGGTGGCTGCGTGGCCGCCTCACTTCGCGC______CGCTAGGCTGGGGGAGTTGATTTGCAC GGCGCGT G AHI1 Ensembl:ENSG00000135541 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:135497489..135497689 26863196 MeRIP-seq:(Medium) rs999588584 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4865026,Human_RBP_ID_18425728 Human_Splice_Rec_815249,Human_Splice_Rec_815305,Human_Splice_Rec_815357,Human_Splice_Rec_815495,Human_Splice_Rec_815543,Human_Splice_Rec_815591,Human_Splice_Rec_815599,Human_Splice_Rec_815615 RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_28256 86733 RMVar_ID_86733 Human_SNP_ID_297769842 m1A Human chr6 + 135532781 135532773 135532782 GGAGGAAGAGGAAGAGGAGGAGGAAGAGGAAGAGGAGGAGGAAGAGGAGGAAGAGGAAGAGGAGG GGAGGAAGAGGAAGAGGAGGAGGAA_________GAGGAGGAAGAGGAGGAAGAGGAAGAGGAGG AGAGGAAGAG A LINC00271 Ensembl:ENSG00000231028 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:135532735..135532869 26863196 MeRIP-seq:(Medium) rs1333694051 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_8271352 86734 RMVar_ID_86734 Human_SNP_ID_297869989 m1A Human chr6 + 135956944 135956944 135956944 ACGAAAAGAAAAGTCAGAAAGGCTGGTGGAGGATATGACAGTACCTCTCAAAGTCTGCCGTCAGG ACGAAAAGAAAAGTCAGAAAGGCTGGTGGAGGGTATGACAGTACCTCTCAAAGTCTGCCGTCAGG A G PDE7B Ensembl:ENSG00000171408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:135956739..135957138 26863196 MeRIP-seq:(Medium) rs1292165384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81862 RMVar_hsa_circ_71693 86735 RMVar_ID_86735 Human_SNP_ID_297873261 m1A Human chr6 + 135970841 135970841 135970841 TAGTGGGGCAGCGAGACGTTTGGATCCAGGCAATATTTTGAAGGTAGAGCTGATAATATTTGCCA TAGTGGGGCAGCGAGACGTTTGGATCCAGGCAGTATTTTGAAGGTAGAGCTGATAATATTTGCCA A G PDE7B Ensembl:ENSG00000171408 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:135970822..135970958 26863196 MeRIP-seq:(Medium) rs956766326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2976101 RMVar_hsa_circ_71693 86736 RMVar_ID_86736 Human_SNP_ID_297940196 m1A Human chr6 - 136248046 136248046 136248046 TTTTTTAAAGCAAAAGTAAGTTGAAGAATCATAGTACCATTATTATAAATGGGCATCTTAGTATG TTTTTTAAAGCAAAAGTAAGTTGAAGAATCATGGTACCATTATTATAAATGGGCATCTTAGTATG T C MTFR2 Ensembl:ENSG00000146410 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:136248044..136248127 26863196 MeRIP-seq:(Medium) rs1397403937 Functional Loss SNV dbSNP153 33..33 33 - - - 86737 RMVar_ID_86737 Human_SNP_ID_297945644 m1A Human chr6 - 136267127 136267127 136267127 GAGGAAGAGCCAGAGGAGTTTTTGCTGGGACAAATACTGGTCCAAACAACTCAAATACTACTTTT GAGGAAGAGCCAGAGGAGTTTTTGCTGGGACAGATACTGGTCCAAACAACTCAAATACTACTTTT T C BCLAF1 Ensembl:ENSG00000029363 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:136261416..136268254 32194978 MeRIP-seq:(Medium) rs1325041000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78908,Human_RBP_ID_4865236,Human_RBP_ID_7546253,Human_RBP_ID_8896564,Human_RBP_ID_17304767,Human_RBP_ID_17418219,Human_RBP_ID_17533753,Human_RBP_ID_22829601,Human_RBP_ID_24548493,Human_RBP_ID_27088353,Human_RBP_ID_27828048 Human_Splice_Rec_815978,Human_Splice_Rec_815979,Human_Splice_Rec_816006,Human_Splice_Rec_816007,Human_Splice_Rec_816082,Human_Splice_Rec_816083,Human_Splice_Rec_816106,Human_Splice_Rec_816107,Human_Splice_Rec_816130,Human_Splice_Rec_816131,Human_Splice_Rec_816158,Human_Splice_Rec_816159,Human_Splice_Rec_816218,Human_Splice_Rec_816219,Human_Splice_Rec_816228,Human_Splice_Rec_816229,Human_Splice_Rec_816252,Human_Splice_Rec_816253 RMVar_hsa_circ_366015,RMVar_hsa_circ_17134,RMVar_hsa_circ_55104,RMVar_hsa_circ_367097,RMVar_hsa_circ_241692 86738 RMVar_ID_86738 Human_SNP_ID_297969565 m1A Human chr6 - 136360787 136360785 136360788 ACGCCGACCTTCTGTTTTCAGAAAGAAGAAGAAGCTCGCGTTCGTGAAGAAGCAGAGAGGGTCCG ACGCCGACCTTCTGTTTTCAGAAAGAAGAAG___CTCGCGTTCGTGAAGAAGCAGAGAGGGTCCG GCTT G MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:136360652..136366031;chr6:136360665..136360833;chr6:136359801..136366025 26863196 MeRIP-seq:(Medium) rs143950846 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_816336,Human_Splice_Rec_816337,Human_Splice_Rec_816370,Human_Splice_Rec_816371,Human_Splice_Rec_816400,Human_Splice_Rec_816401,Human_Splice_Rec_816432,Human_Splice_Rec_816433,Human_Splice_Rec_816466,Human_Splice_Rec_816467,Human_Splice_Rec_816502,Human_Splice_Rec_816503,Human_Splice_Rec_816536,Human_Splice_Rec_816537,Human_Splice_Rec_816568,Human_Splice_Rec_816569,Human_Splice_Rec_816596,Human_Splice_Rec_816597 RMVar_hsa_circ_59035,RMVar_hsa_circ_269019,RMVar_hsa_circ_366845,RMVar_hsa_circ_266974,RMVar_hsa_circ_75044,RMVar_hsa_circ_241700,RMVar_hsa_circ_369188 86739 RMVar_ID_86739 Human_SNP_ID_297969688 m1A Human chr6 - 136361027 136361027 136361027 GGCGGAGGAGCGGGCGCTGCGCGAGCGGGAGGAGGCAGAGCGCGCCCAGAGGCAGGTGCGGCCGC GGCGGAGGAGCGGGCGCTGCGCGAGCGGGAGGGGGCAGAGCGCGCCCAGAGGCAGGTGCGGCCGC T C MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:136361001..136361075 26863196 MeRIP-seq:(Medium) rs758491463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_816335,Human_Splice_Rec_816369,Human_Splice_Rec_816399,Human_Splice_Rec_816431,Human_Splice_Rec_816465,Human_Splice_Rec_816501,Human_Splice_Rec_816535,Human_Splice_Rec_816567,Human_Splice_Rec_816595 RMVar_hsa_circ_59035,RMVar_hsa_circ_269019,RMVar_hsa_circ_366845,RMVar_hsa_circ_266974,RMVar_hsa_circ_75044,RMVar_hsa_circ_241700,RMVar_hsa_circ_369188,RMVar_hsa_circ_265139 86740 RMVar_ID_86740 Human_SNP_ID_297972347 m1A Human chr6 + 136372575 136372575 136372575 TGGTGTTACAAAGAGTTTTGGTCGATCCATCGAATTTCTAGAGTGTGCAGCTTTGTAGGGCATGA TGGTGTTACAAAGAGTTTTGGTCGATCCATCGGATTTCTAGAGTGTGCAGCTTTGTAGGGCATGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:136372447..136372673 26863196 MeRIP-seq:(Medium) rs1423525328 Functional Loss SNV dbSNP153 33..33 33 - - - 86741 RMVar_ID_86741 Human_SNP_ID_297976012 m1A Human chr6 - 136389476 136389476 136389476 AAATAGTGTGGTTAGAAAGAGAAGAGCGAGCCAGGCAGCACTACGAGAAGCACCTGGAAGAGCGG AAATAGTGTGGTTAGAAAGAGAAGAGCGAGCCCGGCAGCACTACGAGAAGCACCTGGAAGAGCGG T G MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:136389426..136389475 26863196 MeRIP-seq:(Medium) rs756769767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5617362 Human_Splice_Rec_816318,Human_Splice_Rec_816352,Human_Splice_Rec_816416,Human_Splice_Rec_816448,Human_Splice_Rec_816484,Human_Splice_Rec_816518,Human_Splice_Rec_816552 Human_miRNA_ID_2082886,Human_miRNA_ID_2774036 RMVar_hsa_circ_24411,RMVar_hsa_circ_59035,RMVar_hsa_circ_265139,RMVar_hsa_circ_266867,RMVar_hsa_circ_296571,RMVar_hsa_circ_297131,RMVar_hsa_circ_241705,RMVar_hsa_circ_241703,RMVar_hsa_circ_241702,RMVar_hsa_circ_285301,RMVar_hsa_circ_241706,RMVar_hsa_circ_296001 86742 RMVar_ID_86742 Human_SNP_ID_297983631 m1A Human chr6 + 136421750 136421750 136421750 TGGTTGTTATTTTGTCCTGAAATTGCAGAGGCAGGGCGGCTGGAGGCATTTTTCTTATCTTGCAC TGGTTGTTATTTTGTCCTGAAATTGCAGAGGCCGGGCGGCTGGAGGCATTTTTCTTATCTTGCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr6:136421644..136466785;chr6:136421701..136421775;chr6:136421655..136421845;chr6:136421620..136421862 26863196 MeRIP-seq:(Medium) rs200819156 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 86743 RMVar_ID_86743 Human_SNP_ID_298012562 m1A Human chr6 + 136550391 136550391 136550391 GCGCCGTCGCCGCCCCTGTGGCCGTCGCCGCCAGCTCCTAGCTCCGCCATGGTGCTCCGATGACG GCGCCGTCGCCGCCCCTGTGGCCGTCGCCGCCCGCTCCTAGCTCCGCCATGGTGCTCCGATGACG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:136526637..136550475 26863196 MeRIP-seq:(Medium) rs753680368 Functional Loss SNV dbSNP153 33..33 33 - - - 86744 RMVar_ID_86744 Human_SNP_ID_298012563 m1A Human chr6 - 136550394 136550394 136550394 GCGCGTCATCGGAGCACCATGGCGGAGCTAGGAGCTGGCGGCGACGGCCACAGGGGCGGCGACGG GCGCGTCATCGGAGCACCATGGCGGAGCTAGGTGCTGGCGGCGACGGCCACAGGGGCGGCGACGG T A MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:136526637..136550506;chr6:136526637..136550475 26863196 MeRIP-seq:(Medium) rs1490147803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81756 Human_Splice_Rec_816381,Human_Splice_Rec_816411,Human_Splice_Rec_816443 86745 RMVar_ID_86745 Human_SNP_ID_298068289 m1A Human chr6 + 136791911 136791910 136791911 CACCGTGGTCCGTCGGCTGCCCCCGCCAACAGAGCTGCCCCGGCCTCGGGTGGCACTGCTCGAGG CACCGTGGTCCGTCGGCTGCCCCCGCCAACAG_GCTGCCCCGGCCTCGGGTGGCACTGCTCGAGG GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:136791865..136791981 26863196 MeRIP-seq:(Medium) rs755168115 Functional Loss DEL dbSNP153 33..33 33 - - - 86746 RMVar_ID_86746 Human_SNP_ID_298068408 m1A Human chr6 - 136792189 136792189 136792189 GTGGCTGGCCAGGCGGTGCGGCTGGGCGGGGGACGCCGCCGCCGTTGCTGCCCGGCCCGGAGAGA GTGGCTGGCCAGGCGGTGCGGCTGGGCGGGGGTCGCCGCCGCCGTTGCTGCCCGGCCCGGAGAGA T A MAP3K5 Ensembl:ENSG00000197442 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:136792145..136792468 26863196 MeRIP-seq:(Medium) rs879218701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17161583 RMVar_hsa_circ_126949,RMVar_hsa_circ_241748,RMVar_hsa_circ_241753,RMVar_hsa_circ_76299 86747 RMVar_ID_86747 Human_SNP_ID_298068409 m1A Human chr6 - 136792189 136792189 136792189 GTGGCTGGCCAGGCGGTGCGGCTGGGCGGGGGACGCCGCCGCCGTTGCTGCCCGGCCCGGAGAGA GTGGCTGGCCAGGCGGTGCGGCTGGGCGGGGGGCGCCGCCGCCGTTGCTGCCCGGCCCGGAGAGA T C MAP3K5 Ensembl:ENSG00000197442 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:136792145..136792468 26863196 MeRIP-seq:(Medium) rs879218701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17161583 RMVar_hsa_circ_126949,RMVar_hsa_circ_241748,RMVar_hsa_circ_241753,RMVar_hsa_circ_76299 86748 RMVar_ID_86748 Human_SNP_ID_298068433 m1A Human chr6 - 136792279 136792259 136792280 GGCGCCGGAGAGGAGGCGGCGGCGCGGCGGCGAGGGCGCGGCGCGCGATGGCAGCTGCTTAGCCC GGCGCCGGAGAGGAGGCGGCGGCGCGGCGGC_____________________AGCTGCTTAGCCC TGCCATCGCGCGCCGCGCCCTC T MAP3K5 Ensembl:ENSG00000197442 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr6:136791830..136792518;chr6:136791823..136792427;chr6:136792121..136792518 26863196 MeRIP-seq:(Medium) rs1185660889 Functional Loss DEL dbSNP153 32..52 33 - - - RMVar_hsa_circ_126949,RMVar_hsa_circ_241748,RMVar_hsa_circ_241753,RMVar_hsa_circ_76299 86749 RMVar_ID_86749 Human_SNP_ID_298068629 m1A Human chr6 - 136792802 136792802 136792802 CGTCTGCAAGGAACGACGAGGCTGGCGCCGGGACCACGCGGCGGAGGCGATCGAAAGAGAAACGA CGTCTGCAAGGAACGACGAGGCTGGCGCCGGGGCCACGCGGCGGAGGCGATCGAAAGAGAAACGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:136792736..136793059 26863196 MeRIP-seq:(Medium) rs1171884157 Functional Loss SNV dbSNP153 33..33 33 - - - 86750 RMVar_ID_86750 Human_SNP_ID_298068666 m1A Human chr6 + 136792904 136792904 136792904 GTAGCGGCACCGAGGGTCAGGGCCAGCCCCCAAGGAGGGCGCTGCTAGGAAGCTCGAGCCCGGAC GTAGCGGCACCGAGGGTCAGGGCCAGCCCCCAGGGAGGGCGCTGCTAGGAAGCTCGAGCCCGGAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:136792810..136792947 26863196 MeRIP-seq:(Medium) rs1000988565 Functional Loss SNV dbSNP153 33..33 33 - - - 86751 RMVar_ID_86751 Human_SNP_ID_298068683 m1A Human chr6 - 136792982 136792982 136792982 GGTGAAGACTGGGACCCTATGCCACGCGCAGCACTCAGAGGAGGGCTGGGGTCCCAGGGCCGCAG GGTGAAGACTGGGACCCTATGCCACGCGCAGCCCTCAGAGGAGGGCTGGGGTCCCAGGGCCGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:136792760..136793059 26863196 MeRIP-seq:(Medium) rs529197842 Functional Loss SNV dbSNP153 33..33 33 - - - 86752 RMVar_ID_86752 Human_SNP_ID_298075497 m1A Human chr6 - 136822626 136822626 136822626 GCCGCCCCCGGCCCTCGCTGCCCCGGCCGCGGAAGCCGTTCCGAGTCGGAGGCACACTGGCGCGG GCCGCCCCCGGCCCTCGCTGCCCCGGCCGCGGTAGCCGTTCCGAGTCGGAGGCACACTGGCGCGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:136822582..136822734 26863196 MeRIP-seq:(Medium) rs1182038401 Functional Loss SNV dbSNP153 33..33 33 - - - 86753 RMVar_ID_86753 Human_SNP_ID_298168478 m1A Human chr6 + 137207077 137207069 137207078 AGGATTCAATTGTAACATTAGTTGGTGTAGGCACTGTAAGAAAATAAAAAAGTAAAAGGGACAAT AGGATTCAATTGTAACATTAGTTGG_________TGTAAGAAAATAAAAAAGTAAAAGGGACAAT GTGTAGGCAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:137207044..137207130 26863196 MeRIP-seq:(Medium) rs753213766 Functional Loss DEL dbSNP153 26..34 33 - - - 86754 RMVar_ID_86754 Human_SNP_ID_298171278 m1A Human chr6 - 137219346 137219346 137219346 GGCTGGTCCCGCAGGCGCTCGGGGTTGGAGCCAGCGACCGTCGGTAGCAGCATGGCTCTCCTCTT GGCTGGTCCCGCAGGCGCTCGGGGTTGGAGCCGGCGACCGTCGGTAGCAGCATGGCTCTCCTCTT T C IFNGR1 Ensembl:ENSG00000027697 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:137219211..137219373 26863196 MeRIP-seq:(Medium) rs372372230 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_791867,Human_RBP_ID_840790,Human_RBP_ID_4903519,Human_RBP_ID_22462237 86755 RMVar_ID_86755 Human_SNP_ID_298338103 m1A Human chr6 + 137879093 137879093 137879093 GCTTCAAAAGGACTACAGCAGAGGCCTCCTCCAGCCTCAGCACCAGCCTCCCTCCTTCCTGTCAC GCTTCAAAAGGACTACAGCAGAGGCCTCCTCCGGCCTCAGCACCAGCCTCCCTCCTTCCTGTCAC A G TNFAIP3 Ensembl:ENSG00000118503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:137879045..137879186 26863196 MeRIP-seq:(Medium) rs767130578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22105403 86756 RMVar_ID_86756 Human_SNP_ID_298394685 m1A Human chr6 + 138107300 138107300 138107300 AGGCGATGGCGCTGAGTAGGAGCAGGGGCAGGATCCAGCGGCAGCGCTCGCAGGCCAGGCCGCAG AGGCGATGGCGCTGAGTAGGAGCAGGGGCAGGTTCCAGCGGCAGCGCTCGCAGGCCAGGCCGCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:138096333..138107475;chr6:138096360..138107461;chr6:138107080..138107475;chr6:138096401..138107511 26863196 MeRIP-seq:(Medium) rs763927344 Functional Loss SNV dbSNP153 33..33 33 - - - 86757 RMVar_ID_86757 Human_SNP_ID_298394739 m1A Human chr6 + 138107378 138107378 138107378 CGGGCGGCGCGGGGCCGAGCGGAGCGGAGCGGAGCGGGTCGGAGGAGCGCGCGGGACGGGCGACA CGGGCGGCGCGGGGCCGAGCGGAGCGGAGCGGCGCGGGTCGGAGGAGCGCGCGGGACGGGCGACA A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:138107302..138107386 26863410 MeRIP-seq:(Medium) rs1053043867 Functional Loss SNV dbSNP153 33..33 33 - - - 86758 RMVar_ID_86758 Human_SNP_ID_298394747 m1A Human chr6 - 138107384 138107384 138107384 CTCTGCTGTCGCCCGTCCCGCGCGCTCCTCCGACCCGCTCCGCTCCGCTCCGCTCGGCCCCGCGC CTCTGCTGTCGCCCGTCCCGCGCGCTCCTCCGCCCCGCTCCGCTCCGCTCCGCTCGGCCCCGCGC T G PERP Ensembl:ENSG00000112378 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:138107276..138107500 26863410 MeRIP-seq:(Medium) rs757998269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252064,Human_RBP_ID_4865736,Human_RBP_ID_22461449 86759 RMVar_ID_86759 Human_SNP_ID_298466002 m1A Human chr6 + 138404359 138404359 138404359 GAGGCAGACGCATCGGGTGGGCTCGGGTCTCCAGCCCGGCCGGGAGGAGGGACCGGGTCTGCGGA GAGGCAGACGCATCGGGTGGGCTCGGGTCTCCGGCCCGGCCGGGAGGAGGGACCGGGTCTGCGGA A G HEBP2 Ensembl:ENSG00000051620 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr6:138404259..138404482;chr6:138404268..138404549 26863196,26863410 MeRIP-seq:(Medium) rs1346836756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903524,Human_RBP_ID_5427878,Human_RBP_ID_17671971,Human_RBP_ID_26354442 86760 RMVar_ID_86760 Human_SNP_ID_298466016 m1A Human chr6 - 138404386 138404386 138404386 CGCCCCGCCGAGGCCCCGAGTCCCCGCTCCGCAGACCCGGTCCCTCCTCCCGGCCGGGCTGGAGA CGCCCCGCCGAGGCCCCGAGTCCCCGCTCCGCCGACCCGGTCCCTCCTCCCGGCCGGGCTGGAGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:138404252..138404597 26863196 MeRIP-seq:(Medium) rs1377218181 Functional Loss SNV dbSNP153 33..33 33 - - - 86761 RMVar_ID_86761 Human_SNP_ID_298466040 m1A Human chr6 - 138404446 138404446 138404446 TGGGAGCCTGGTCAGCCGCGCAGAGGCCCCGCACCCCGGGCCGCCCCGCCTGCGTGTGCGCGCCC TGGGAGCCTGGTCAGCCGCGCAGAGGCCCCGCCCCCCGGGCCGCCCCGCCTGCGTGTGCGCGCCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:138404285..138404575 26863410 MeRIP-seq:(Medium) rs991765585 Functional Loss SNV dbSNP153 33..33 33 - - - 86762 RMVar_ID_86762 Human_SNP_ID_298466057 m1A Human chr6 + 138404496 138404496 138404496 CTGACCAGGCTCCCAGAGCGTCAGCGCCGCCCATGGCCGAGCCGCTCCAGCCAGACCCCGGGGCG CTGACCAGGCTCCCAGAGCGTCAGCGCCGCCCGTGGCCGAGCCGCTCCAGCCAGACCCCGGGGCG A G HEBP2 Ensembl:ENSG00000051620 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:138404283..138404625 26863410 MeRIP-seq:(Medium) rs1039969885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903524,Human_RBP_ID_26355596,Human_RBP_ID_26829948 86763 RMVar_ID_86763 Human_SNP_ID_298466091 m1A Human chr6 + 138404571 138404570 138404571 CGGCGGCCCAAGCTGTGGAGACGCCGGGCTGGAAGGCCCCGGAGGACGCCGGCCCCCAGGTAGGC CGGCGGCCCAAGCTGTGGAGACGCCGGGCTGG_AGGCCCCGGAGGACGCCGGCCCCCAGGTAGGC GA G HEBP2 Ensembl:ENSG00000051620 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1246750989 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_790768,Human_RBP_ID_4903524,Human_RBP_ID_17663432,Human_RBP_ID_22462241,Human_RBP_ID_26828804 Human_Splice_Rec_817249,Human_Splice_Rec_817255 86764 RMVar_ID_86764 Human_SNP_ID_298534218 m1A Human chr6 - 138692556 138692556 138692556 CGAGCTCGAGGGCCAGGCGGCCGCGCTGGGCCACCGCACCGCCGCGCTGCACCGCCGCCTCGACG CGAGCTCGAGGGCCAGGCGGCCGCGCTGGGCCGCCGCACCGCCGCGCTGCACCGCCGCCTCGACG T C NHSL1 Ensembl:ENSG00000135540 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:138692508..138694347;chr6:138692508..138692657;chr6:138692508..138692719 26863196 MeRIP-seq:(Medium) rs1401391400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_817305,Human_Splice_Rec_817325 86765 RMVar_ID_86765 Human_SNP_ID_298534237 m1A Human chr6 + 138692608 138692608 138692608 GCCCTCGAGCTCGCCGAAGATGTCCCCGGCGCAGCGCGACAGGTCGGCCAGCTGCGCCAGCAGGC GCCCTCGAGCTCGCCGAAGATGTCCCCGGCGCGGCGCGACAGGTCGGCCAGCTGCGCCAGCAGGC A G AL590617.2 Ensembl:ENSG00000225177 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:138692511..138692625 26863410 MeRIP-seq:(Medium) rs780946921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_817327 86766 RMVar_ID_86766 Human_SNP_ID_298534238 m1A Human chr6 + 138692608 138692608 138692608 GCCCTCGAGCTCGCCGAAGATGTCCCCGGCGCAGCGCGACAGGTCGGCCAGCTGCGCCAGCAGGC GCCCTCGAGCTCGCCGAAGATGTCCCCGGCGCTGCGCGACAGGTCGGCCAGCTGCGCCAGCAGGC A T AL590617.2 Ensembl:ENSG00000225177 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:138692511..138692625 26863410 MeRIP-seq:(Medium) rs780946921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_817327 86767 RMVar_ID_86767 Human_SNP_ID_298534348 m1A Human chr6 + 138692952 138692944 138692952 GAAGGACGGACGGACGGACGGGCGCGCGGGCGAGCGGGCACCCGGGCGGCGCGGGGCAGGAATGG GAAGGACGGACGGACGGACGGGCGC________GCGGGCACCCGGGCGGCGCGGGGCAGGAATGG CGCGGGCGA C AL590617.2 Ensembl:ENSG00000225177 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:138692726..138693366;chr6:138692783..138693357 26863196 MeRIP-seq:(Medium) rs947146050 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_950403,Human_RBP_ID_3821809,Human_RBP_ID_4903525,Human_RBP_ID_5218393,Human_RBP_ID_8215360,Human_RBP_ID_8270750,Human_RBP_ID_8730322,Human_RBP_ID_18465614,Human_RBP_ID_26793246 86768 RMVar_ID_86768 Human_SNP_ID_298554035 m1A Human chr6 - 138773842 138773842 138773842 TCCGCAACCCGCAAAGACCCGACAGCCTCAGAAGCCACCGCCGCAGCCACAAGCAGAGCCCCGGT TCCGCAACCCGCAAAGACCCGACAGCCTCAGACGCCACCGCCGCAGCCACAAGCAGAGCCCCGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:138773791..138776131 26863196 MeRIP-seq:(Medium) rs1427903901 Functional Loss SNV dbSNP153 33..33 33 - - - 86769 RMVar_ID_86769 Human_SNP_ID_298643494 m1A Human chr6 - 139135144 139135144 139135144 GCAGCCGCGCGGGCGCCGCGGGCCCGGGGCGCAAGCGAGACGCTCCCGAGCCGGAGGGAAAAGGC GCAGCCGCGCGGGCGCCGCGGGCCCGGGGCGCTAGCGAGACGCTCCCGAGCCGGAGGGAAAAGGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:139135110..139135523 26863196 MeRIP-seq:(Medium) rs1352202402 Functional Loss SNV dbSNP153 33..33 33 - - - 86770 RMVar_ID_86770 Human_SNP_ID_298643521 m1A Human chr6 + 139135231 139135231 139135231 GGCTCCAGGAAGCCGGAGAGGGCGCGGCGGCCAGGATGGCGCGGCACGGGCCGTGCGGCTAGACG GGCTCCAGGAAGCCGGAGAGGGCGCGGCGGCCGGGATGGCGCGGCACGGGCCGTGCGGCTAGACG A G HECA Ensembl:ENSG00000112406 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:139135137..139135250 26863410 MeRIP-seq:(Medium) rs971230670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18065643 86771 RMVar_ID_86771 Human_SNP_ID_298700220 m1A Human chr6 + 139373398 139373374 139373398 GCCGCTGTTGCTGCTGCCCGCGCCGCCGCCCGAGCTGCTGCCAGAGCCGCCGGGGGTGCTGCTGC GCCGCTGTT________________________GCTGCTGCCAGAGCCGCCGGGGGTGCTGCTGC TGCTGCTGCCCGCGCCGCCGCCCGA T AL592429.2 Ensembl:ENSG00000226571 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:139373348..139374172 26863196 MeRIP-seq:(Medium) rs780870084 Functional Loss DEL dbSNP153 10..33 33 - - - 86772 RMVar_ID_86772 Human_SNP_ID_298700239 m1A Human chr6 - 139373425 139373398 139373425 GCAGCAGCACCCCCGGCGGCTCGGGCGGCAGCAGCACCCCCGGCGGCTCTGGCAGCAGCTCGGGC GCAGCAGCACCCCCGGCGGCTCGGGCGGCAGC___________________________TCGGGC AGCTGCTGCCAGAGCCGCCGGGGGTGCT A CITED2 Ensembl:ENSG00000164442 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:139373375..139373605 26863196 MeRIP-seq:(Medium) rs1233484802 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_4866609,Human_RBP_ID_5242591,Human_RBP_ID_22461451 86773 RMVar_ID_86773 Human_SNP_ID_298700301 m1A Human chr6 - 139373469 139373469 139373469 GACAAACCAGCACTTCCGAGATTGCAACCCCAAGCACAGCGGCGGCAGCAGCACCCCCGGCGGCT GACAAACCAGCACTTCCGAGATTGCAACCCCACGCACAGCGGCGGCAGCAGCACCCCCGGCGGCT T G CITED2 Ensembl:ENSG00000164442 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:139373418..139374172 26863196 MeRIP-seq:(Medium) rs928813400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22105409,Human_RBP_ID_24138013 86774 RMVar_ID_86774 Human_SNP_ID_298700508 m1A Human chr6 - 139373791 139373791 139373791 AGCAGCAGCCCCAGCACGCCTTCAACGCCCTAATGGGCGAGCACATACACTACGGCGCGGGCAAC AGCAGCAGCCCCAGCACGCCTTCAACGCCCTAGTGGGCGAGCACATACACTACGGCGCGGGCAAC T C CITED2 Ensembl:ENSG00000164442 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:139373741..139373824 26863196 MeRIP-seq:(Medium) rs755079675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22101353 86775 RMVar_ID_86775 Human_SNP_ID_299379989 m1A Human chr6 - 142147307 142147307 142147307 GTATGCTCTTGAACTGTGCGGGGAGCGGGGGCAGCGGTGCAAGCGCGGCCATCTCTACTCCGAAC GTATGCTCTTGAACTGTGCGGGGAGCGGGGGCGGCGGTGCAAGCGCGGCCATCTCTACTCCGAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:142147256..142147432 26863196 MeRIP-seq:(Medium) rs1330730996 Functional Loss SNV dbSNP153 33..33 33 - - - 86776 RMVar_ID_86776 Human_SNP_ID_299380004 m1A Human chr6 - 142147316 142147316 142147316 GATGATGCTGTATGCTCTTGAACTGTGCGGGGAGCGGGGGCAGCGGTGCAAGCGCGGCCATCTCT GATGATGCTGTATGCTCTTGAACTGTGCGGGGTGCGGGGGCAGCGGTGCAAGCGCGGCCATCTCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:142147267..142147400 26863196 MeRIP-seq:(Medium) rs765716031 Functional Loss SNV dbSNP153 33..33 33 - - - 86777 RMVar_ID_86777 Human_SNP_ID_299380026 m1A Human chr6 + 142147361 142147361 142147361 CAAGAGCATACAGCATCATCTGAGGACGGCTCAGGAGCATGACAAGCGAGACCCTGTGGTGGCTT CAAGAGCATACAGCATCATCTGAGGACGGCTCGGGAGCATGACAAGCGAGACCCTGTGGTGGCTT A G VTA1 Ensembl:ENSG00000009844 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:142147310..142169565 32194978 MeRIP-seq:(Medium) rs770642122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2010042,Human_RBP_ID_4904288,Human_RBP_ID_7551653,Human_RBP_ID_9401186,Human_RBP_ID_15666921,Human_RBP_ID_18425499,Human_RBP_ID_19129758,Human_RBP_ID_26355600,Human_RBP_ID_27828064 Human_Splice_Rec_818303,Human_Splice_Rec_818313,Human_Splice_Rec_818325,Human_Splice_Rec_818337 86778 RMVar_ID_86778 Human_SNP_ID_299398547 m1A Human chr6 + 142220449 142220449 142220449 AGAAACTACGGAGTCCGCTGGTAGTGGGCTGCATGGTGTGACAGAGCCCTTCTCTGTAAAATGGA AGAAACTACGGAGTCCGCTGGTAGTGGGCTGCGTGGTGTGACAGAGCCCTTCTCTGTAAAATGGA A G VTA1 Ensembl:ENSG00000009844 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:142220361..142220611 32194978 MeRIP-seq:(Medium) rs979376400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_654420,Human_RBP_ID_8215773,Human_RBP_ID_8632976,Human_RBP_ID_24138254 86779 RMVar_ID_86779 Human_SNP_ID_299418424 m1A Human chr6 - 142301906 142301906 142301906 AGGTACTTGGGTCCCCCTCGCGGGCGCAGGCGACTCTCCCCGGACCCGTGCGCTCCGCCCGCGCT AGGTACTTGGGTCCCCCTCGCGGGCGCAGGCGTCTCTCCCCGGACCCGTGCGCTCCGCCCGCGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:142301811..142302134;chr6:142301742..142302141;chr6:142301856..142301974 26863196,32194978 MeRIP-seq:(Medium) rs113297468 Functional Loss SNV dbSNP153 33..33 33 - - - 86780 RMVar_ID_86780 Human_SNP_ID_299418425 m1A Human chr6 - 142301906 142301906 142301906 AGGTACTTGGGTCCCCCTCGCGGGCGCAGGCGACTCTCCCCGGACCCGTGCGCTCCGCCCGCGCT AGGTACTTGGGTCCCCCTCGCGGGCGCAGGCGGCTCTCCCCGGACCCGTGCGCTCCGCCCGCGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr6:142301811..142302134;chr6:142301742..142302141;chr6:142301856..142301974 26863196,32194978 MeRIP-seq:(Medium) rs113297468 Functional Loss SNV dbSNP153 33..33 33 - - - 86781 RMVar_ID_86781 Human_SNP_ID_299418484 m1A Human chr6 - 142302052 142302052 142302052 CTCGCAGGGAAGTTGGCAGGGTGAGGGCGAGAAGCTGAGGAAGTAGGGTGTGCGTGGGGCTGGTG CTCGCAGGGAAGTTGGCAGGGTGAGGGCGAGAGGCTGAGGAAGTAGGGTGTGCGTGGGGCTGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:142301758..142302096 26863196 MeRIP-seq:(Medium) rs1367153340 Functional Loss SNV dbSNP153 33..33 33 - - - 86782 RMVar_ID_86782 Human_SNP_ID_299428968 m1A Human chr6 + 142343671 142343671 142343671 TAATAGTAATAATTACCATTGCAAAAAAGAGCAAGAGTCAAATTGAAAAATAGATTTAATTTCCA TAATAGTAATAATTACCATTGCAAAAAAGAGCTAGAGTCAAATTGAAAAATAGATTTAATTTCCA A T ADGRG6 Ensembl:ENSG00000112414 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:142343655..142343742 26863410 MeRIP-seq:(Medium) rs1245132553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69318,RMVar_hsa_circ_103398,RMVar_hsa_circ_241865 86783 RMVar_ID_86783 Human_SNP_ID_299452545 m1A Human chr6 - 142445278 142445278 142445278 CTCAGTGACCTTAGATTTACTATCTTACTTAGAATCTCAGTGACCTTATATTTACTATTCTTTTT CTCAGTGACCTTAGATTTACTATCTTACTTAGGATCTCAGTGACCTTATATTTACTATTCTTTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:142445019..142445618 32194978 MeRIP-seq:(Medium) rs1406096152 Functional Loss SNV dbSNP153 33..33 33 - - - 86784 RMVar_ID_86784 Human_SNP_ID_299603948 m1A Human chr6 - 143060766 143060766 143060766 CGGGGGCGGGGGCGGGGCGCGCGCCCCCGGGGACTGGCGCGGCCGCGAGCGCCCGGGTGACCTGT CGGGGGCGGGGGCGGGGCGCGCGCCCCCGGGGTCTGGCGCGGCCGCGAGCGCCCGGGTGACCTGT T A RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:143060735..143060817 26863410 MeRIP-seq:(Medium) rs1159585245 Functional Loss SNV dbSNP153 33..33 33 - - - 86785 RMVar_ID_86785 Human_SNP_ID_299604123 m1A Human chr6 - 143060966 143060966 143060966 TGTAGTTACACAGGATAGAGCAGTAAGACAGCAGGATTGCCATCCGCAGCACCTGGCAGGGGACA TGTAGTTACACAGGATAGAGCAGTAAGACAGCCGGATTGCCATCCGCAGCACCTGGCAGGGGACA T G RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:143060916..143061048 26863196 MeRIP-seq:(Medium) rs752516493 Functional Loss SNV dbSNP153 33..33 33 - - - 86786 RMVar_ID_86786 Human_SNP_ID_299704313 m1A Human chr6 + 143495808 143495808 143495808 CAGTTCTACCATAATGCCATTTTGCTCCAAAGAAATCCAGTTAAGTGGCTGTCCATGGCCCAGTA CAGTTCTACCATAATGCCATTTTGCTCCAAAGGAATCCAGTTAAGTGGCTGTCCATGGCCCAGTA A G AL031320.2,VDAC1P8 Ensembl:ENSG00000278206,Ensembl:ENSG00000229036 lincRNA,Pseudogene intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:143495558..143497012 32194978 MeRIP-seq:(Medium) rs754694312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 86787 RMVar_ID_86787 Human_SNP_ID_299705621 m1A Human chr6 + 143501969 143501969 143501969 ATCTGGGGTGACAGTGTCATTCTGGGATCGCCAGGTATGGGTTTCATAAATAGCTTCTCCATTGA ATCTGGGGTGACAGTGTCATTCTGGGATCGCCGGGTATGGGTTTCATAAATAGCTTCTCCATTGA A G AL031320.2,VDAC1P8 Ensembl:ENSG00000278206,Ensembl:ENSG00000229036 lincRNA,Pseudogene intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:143497410..143501994 32194978 MeRIP-seq:(Medium) rs772074005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 86788 RMVar_ID_86788 Human_SNP_ID_299708023 m1A Human chr6 + 143511576 143511570 143511576 CGCTGTGGGCAGGGCACGGCGGCGGCGGCAGCAGCAGCAACAGCAACAGCAGCAACGGGAACGCG CGCTGTGGGCAGGGCACGGCGGCGGCG______GCAGCAACAGCAACAGCAGCAACGGGAACGCG GGCAGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:143511440..143511700 26863196 MeRIP-seq:(Medium) rs750441314 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_241906 86789 RMVar_ID_86789 Human_SNP_ID_299708028 m1A Human chr6 + 143511576 143511576 143511576 CGCTGTGGGCAGGGCACGGCGGCGGCGGCAGCAGCAGCAACAGCAACAGCAGCAACGGGAACGCG CGCTGTGGGCAGGGCACGGCGGCGGCGGCAGCGGCAGCAACAGCAACAGCAGCAACGGGAACGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:143511440..143511700 26863196 MeRIP-seq:(Medium) rs1007087949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 86790 RMVar_ID_86790 Human_SNP_ID_299708030 m1A Human chr6 + 143511589 143511577 143511589 GCACGGCGGCGGCGGCAGCAGCAGCAACAGCAACAGCAGCAACGGGAACGCGAGCCTGGGGAGCT GCACGGCGGCGGCGGCAGCAG____________CAGCAGCAACGGGAACGCGAGCCTGGGGAGCT GCAGCAACAGCAA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:143511539..143511640 32194978 MeRIP-seq:(Medium) rs781434054 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_241906 86791 RMVar_ID_86791 Human_SNP_ID_299708037 m1A Human chr6 + 143511589 143511589 143511589 GCACGGCGGCGGCGGCAGCAGCAGCAACAGCAACAGCAGCAACGGGAACGCGAGCCTGGGGAGCT GCACGGCGGCGGCGGCAGCAGCAGCAACAGCAGCAGCAGCAACGGGAACGCGAGCCTGGGGAGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:143511539..143511640 32194978 MeRIP-seq:(Medium) rs1333044384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 86792 RMVar_ID_86792 Human_SNP_ID_299708064 m1A Human chr6 - 143511658 143511658 143511658 CAGCGCTCCCGAGGCCGCGGGAGCCTGCAGAGAGGACAGCCGGCCTGCGCCGGGACATGCGGCCC CAGCGCTCCCGAGGCCGCGGGAGCCTGCAGAGCGGACAGCCGGCCTGCGCCGGGACATGCGGCCC T G FUCA2 Ensembl:ENSG00000001036 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:143511449..143511725;chr6:143511426..143511725;chr6:143511476..143511725;chr6:143511476..143511700;chr6:143511526..143511725 31548705,26863196 m1A-IP-seq:(High) rs1451935054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251910,Human_RBP_ID_791827,Human_RBP_ID_840721,Human_RBP_ID_4867227,Human_RBP_ID_24548826 86793 RMVar_ID_86793 Human_SNP_ID_299709373 m1A Human chr6 + 143516891 143516887 143516891 CTGGGCAAGAGGGAGAAAGGAGATGAAAGAAAAAAAGAAAGAAAAGAAAAGAAGGAAGGAAAAGA CTGGGCAAGAGGGAGAAAGGAGATGAAAG____AAAGAAAGAAAAGAAAAGAAGGAAGGAAAAGA GAAAA G HSALNG0054037 RNACentral:URS0000EBD54B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:143516840..143516954 26863196 MeRIP-seq:(Medium) rs939666073 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_241906 86794 RMVar_ID_86794 Human_SNP_ID_299709374 m1A Human chr6 + 143516891 143516887 143516891 CTGGGCAAGAGGGAGAAAGGAGATGAAAGAAAAAAAGAAAGAAAAGAAAAGAAGGAAGGAAAAGA CTGGGCAAGAGGGAGAAAGGAGATGAAAGAAA_AAAGAAAGAAAAGAAAAGAAGGAAGGAAAAGA GAAAA GAAA HSALNG0054037 RNACentral:URS0000EBD54B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:143516840..143516954 26863196 MeRIP-seq:(Medium) rs939666073 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 86795 RMVar_ID_86795 Human_SNP_ID_299709451 m1A Human chr6 + 143516974 143516962 143516974 GAAGGAAGGAAGGAAGGAAGGAAGGAGAAGGAAAGAAGGAAAGAAAAAAGAAAGAAAGGAAAGAA GAAGGAAGGAAGGAAGGAAGG____________AGAAGGAAAGAAAAAAGAAAGAAAGGAAAGAA GAAGGAGAAGGAA G HSALNG0054037 RNACentral:URS0000EBD54B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:143516924..143517011 26863196 MeRIP-seq:(Medium) rs1025185600 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_241906 86796 RMVar_ID_86796 Human_SNP_ID_299709454 m1A Human chr6 + 143516974 143516966 143516974 GAAGGAAGGAAGGAAGGAAGGAAGGAGAAGGAAAGAAGGAAAGAAAAAAGAAAGAAAGGAAAGAA GAAGGAAGGAAGGAAGGAAGGAAGG________AGAAGGAAAGAAAAAAGAAAGAAAGGAAAGAA GAGAAGGAA G HSALNG0054037 RNACentral:URS0000EBD54B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:143516924..143517011 26863196 MeRIP-seq:(Medium) rs1042841344 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_241906 86797 RMVar_ID_86797 Human_SNP_ID_299761900 m1A Human chr6 - 143744620 143744620 143744620 TGGGGCCCTGCATGGTGGCCTCTGTCCTTCCCAGGAGGCCATATCCCCAGACAACTGCTAGACTC TGGGGCCCTGCATGGTGGCCTCTGTCCTTCCCGGGAGGCCATATCCCCAGACAACTGCTAGACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:143744618..143744738 26863196 MeRIP-seq:(Medium) rs778099560 Functional Loss SNV dbSNP153 33..33 33 - - - 86798 RMVar_ID_86798 Human_SNP_ID_299790036 m1A Human chr6 + 143863435 143863431 143863435 TGTACTTATAACAGGAACGAAGAGTGGAGAAGAAAGCTAACAAATTAGCATTTAAACTGGAGAAA TGTACTTATAACAGGAACGAAGAGTGGAG____AAGCTAACAAATTAGCATTTAAACTGGAGAAA GAAGA G AL049844.3,LTV1 Ensembl:ENSG00000280148,Ensembl:ENSG00000135521 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:143863419..143863537 26863196 MeRIP-seq:(Medium) rs1323532060 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_950111,Human_RBP_ID_1678535,Human_RBP_ID_5532767,Human_RBP_ID_9350689,Human_RBP_ID_23067639,Human_RBP_ID_24139001,Human_RBP_ID_24548499,Human_RBP_ID_27828080 Human_Splice_Rec_819152 RMVar_hsa_circ_43707 86799 RMVar_ID_86799 Human_SNP_ID_299808225 m1A Human chr6 + 143941992 143941992 143941992 GGAGGGAGGCCAGGGACTCTGGCAGCGGCTGCATAGGCTGGGCGGCTTGTTCTGGGGGACTGAGG GGAGGGAGGCCAGGGACTCTGGCAGCGGCTGCTTAGGCTGGGCGGCTTGTTCTGGGGGACTGAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:143941845..143942074 26863196 MeRIP-seq:(Medium) rs1345314857 Functional Loss SNV dbSNP153 33..33 33 - - - 86800 RMVar_ID_86800 Human_SNP_ID_299812164 m1A Human chr6 + 143959123 143959123 143959123 CCCGTCGCCCCGGAGGCCGGCACCTTGCTCACAATAAGCCTCAATTTCCCACCGCTGCCTGCTCG CCCGTCGCCCCGGAGGCCGGCACCTTGCTCACGATAAGCCTCAATTTCCCACCGCTGCCTGCTCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:143959121..143959210 26863196 MeRIP-seq:(Medium) rs560005223 Functional Loss SNV dbSNP153 33..33 33 - - - 86801 RMVar_ID_86801 Human_SNP_ID_299843211 m1A Human chr6 + 144095075 144095072 144095075 CCCAGTGCTGTTCTAAGGGTCCACATGAAGGCAGGTCAGGCGGGACTCCCCGGGCAAGCACTTCT CCCAGTGCTGTTCTAAGGGTCCACATGAAG___GGTCAGGCGGGACTCCCCGGGCAAGCACTTCT GGCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:144095026..144095075 32194978 MeRIP-seq:(Medium) rs1163508449 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5450555,Human_RBP_ID_18066354 86802 RMVar_ID_86802 Human_SNP_ID_299843359 m1A Human chr6 + 144095485 144095485 144095485 CTGCAGGTGCTCCAGCTGGCTATGGATGGTGTAGCGGTCAGTCATCTCGCCGCTTTCCCCTTCGC CTGCAGGTGCTCCAGCTGGCTATGGATGGTGTGGCGGTCAGTCATCTCGCCGCTTTCCCCTTCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:144095437..144095575 26863196 MeRIP-seq:(Medium) rs1244626251 Functional Loss SNV dbSNP153 33..33 33 - - - 86803 RMVar_ID_86803 Human_SNP_ID_299843368 m1A Human chr6 - 144095513 144095513 144095513 GTTGTTACCTGCGTCCTCTGACCTGAGAGCGAAGGGGAAAGCGGCGAGATGACTGACCGCTACAC GTTGTTACCTGCGTCCTCTGACCTGAGAGCGAGGGGGAAAGCGGCGAGATGACTGACCGCTACAC T C SF3B5 Ensembl:ENSG00000169976 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:144095426..144095625 26863196 MeRIP-seq:(Medium) rs775661367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_654778,Human_RBP_ID_1665244,Human_RBP_ID_4867484,Human_RBP_ID_5427928,Human_RBP_ID_5478753,Human_RBP_ID_8633412,Human_RBP_ID_9336778,Human_RBP_ID_9401228,Human_RBP_ID_18855755,Human_RBP_ID_22462255,Human_RBP_ID_26771959,Human_RBP_ID_26828827,Human_RBP_ID_27341414 86804 RMVar_ID_86804 Human_SNP_ID_299843369 m1A Human chr6 - 144095514 144095514 144095514 AGTTGTTACCTGCGTCCTCTGACCTGAGAGCGAAGGGGAAAGCGGCGAGATGACTGACCGCTACA AGTTGTTACCTGCGTCCTCTGACCTGAGAGCGGAGGGGAAAGCGGCGAGATGACTGACCGCTACA T C SF3B5 Ensembl:ENSG00000169976 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:144095368..144095625 26863196 MeRIP-seq:(Medium) rs548673819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_654778,Human_RBP_ID_1665244,Human_RBP_ID_4867484,Human_RBP_ID_5427928,Human_RBP_ID_5478753,Human_RBP_ID_8633412,Human_RBP_ID_9336778,Human_RBP_ID_9401228,Human_RBP_ID_18855755,Human_RBP_ID_22462255,Human_RBP_ID_26771959,Human_RBP_ID_26828827,Human_RBP_ID_27341414 86805 RMVar_ID_86805 Human_SNP_ID_299888987 m1A Human chr6 + 144285002 144285002 144285002 ACCGCCGAGGCCCGGCAGACGCTGACCCGGGAACGTAGTGGGGCTGATCTTCCGGAACAAAGTTG ACCGCCGAGGCCCGGCAGACGCTGACCCGGGACCGTAGTGGGGCTGATCTTCCGGAACAAAGTTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:144284956..144285055 26863196 MeRIP-seq:(Medium) rs1294612646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18855762 86806 RMVar_ID_86806 Human_SNP_ID_299894028 m1A Human chr6 - 144306432 144306432 144306432 ACCACCACCATGTCCTATCAGGTCTGCCTCCTACCTAAAGCTTCTAAACTCTCCCCTCTCCTCCT ACCACCACCATGTCCTATCAGGTCTGCCTCCTCCCTAAAGCTTCTAAACTCTCCCCTCTCCTCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:144306329..144306528 26863196 MeRIP-seq:(Medium) rs1353813768 Functional Loss SNV dbSNP153 33..33 33 - - - 86807 RMVar_ID_86807 Human_SNP_ID_299955929 m1A Human chr6 + 144566197 144566197 144566197 TGGAAGATGAAAGGTTCTCCATGCAAGAACTGAGCTTTATGATCTATCGAGCACATTGTCAGTGA TGGAAGATGAAAGGTTCTCCATGCAAGAACTGTGCTTTATGATCTATCGAGCACATTGTCAGTGA A T UTRN Ensembl:ENSG00000152818 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:144566166..144566292 26863196 MeRIP-seq:(Medium) rs1321289867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58410,RMVar_hsa_circ_354446,RMVar_hsa_circ_113273,RMVar_hsa_circ_266103,RMVar_hsa_circ_241927,RMVar_hsa_circ_74259,RMVar_hsa_circ_122016,RMVar_hsa_circ_241933,RMVar_hsa_circ_265084,RMVar_hsa_circ_34125,RMVar_hsa_circ_53592,RMVar_hsa_circ_102797,RMVar_hsa_circ_69731,RMVar_hsa_circ_241937,RMVar_hsa_circ_64399,RMVar_hsa_circ_368526,RMVar_hsa_circ_266496,RMVar_hsa_circ_107311,RMVar_hsa_circ_63531,RMVar_hsa_circ_241950,RMVar_hsa_circ_353902,RMVar_hsa_circ_98765,RMVar_hsa_circ_108124,RMVar_hsa_circ_241954,RMVar_hsa_circ_241955,RMVar_hsa_circ_106954,RMVar_hsa_circ_61678,RMVar_hsa_circ_241959,RMVar_hsa_circ_309890,RMVar_hsa_circ_101489,RMVar_hsa_circ_111050,RMVar_hsa_circ_107129,RMVar_hsa_circ_88162,RMVar_hsa_circ_241964,RMVar_hsa_circ_8868,RMVar_hsa_circ_58460,RMVar_hsa_circ_241966,RMVar_hsa_circ_241965,RMVar_hsa_circ_71180,RMVar_hsa_circ_241962,RMVar_hsa_circ_241963,RMVar_hsa_circ_241973,RMVar_hsa_circ_91640,RMVar_hsa_circ_59537,RMVar_hsa_circ_108582,RMVar_hsa_circ_241975,RMVar_hsa_circ_355142,RMVar_hsa_circ_95859,RMVar_hsa_circ_241977,RMVar_hsa_circ_125753,RMVar_hsa_circ_63968,RMVar_hsa_circ_241979,RMVar_hsa_circ_33996,RMVar_hsa_circ_81705,RMVar_hsa_circ_100668,RMVar_hsa_circ_350193,RMVar_hsa_circ_70923,RMVar_hsa_circ_71317,RMVar_hsa_circ_241980,RMVar_hsa_circ_241983,RMVar_hsa_circ_77748,RMVar_hsa_circ_241984,RMVar_hsa_circ_347043,RMVar_hsa_circ_87648,RMVar_hsa_circ_107781,RMVar_hsa_circ_74391,RMVar_hsa_circ_28940,RMVar_hsa_circ_23581,RMVar_hsa_circ_241987,RMVar_hsa_circ_241988,RMVar_hsa_circ_90589,RMVar_hsa_circ_312401,RMVar_hsa_circ_73724,RMVar_hsa_circ_70114,RMVar_hsa_circ_80350,RMVar_hsa_circ_241989,RMVar_hsa_circ_241990,RMVar_hsa_circ_109685,RMVar_hsa_circ_241995,RMVar_hsa_circ_241996,RMVar_hsa_circ_96163,RMVar_hsa_circ_366326,RMVar_hsa_circ_126152,RMVar_hsa_circ_75063,RMVar_hsa_circ_101294,RMVar_hsa_circ_241997,RMVar_hsa_circ_241998,RMVar_hsa_circ_377213,RMVar_hsa_circ_310614,RMVar_hsa_circ_241999 86808 RMVar_ID_86808 Human_SNP_ID_300210017 m1A Human chr6 - 145625805 145625805 145625805 TATTTAGAAGGCGTGGGGGACAAGAAGGATACAAGGTAAGTTTCAGTGGAGCTCAGAGGACGGGG TATTTAGAAGGCGTGGGGGACAAGAAGGATACGAGGTAAGTTTCAGTGGAGCTCAGAGGACGGGG T C EPM2A Ensembl:ENSG00000112425 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:145625756..145625821 26863196 MeRIP-seq:(Medium) rs1337413598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7554410 86809 RMVar_ID_86809 Human_SNP_ID_300212264 m1A Human chr6 - 145634480 145634480 145634480 AATGGGTAAGAGAGGAGTGAGGACCGTGCTGGAGGAGGGTTATGCATGGGAAGAGCACATTCTGG AATGGGTAAGAGAGGAGTGAGGACCGTGCTGGCGGAGGGTTATGCATGGGAAGAGCACATTCTGG T G EPM2A Ensembl:ENSG00000112425 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:145634462..145634560 26863196 MeRIP-seq:(Medium) rs1438780388 Functional Loss SNV dbSNP153 33..33 33 - - - 86810 RMVar_ID_86810 Human_SNP_ID_300224724 m1A Human chr6 - 145686263 145686263 145686263 CAATGGACCTCATCATGACCGTTGCTGTACTTACAATGAAAACAACTTGGTGGATGGTGTGTATT CAATGGACCTCATCATGACCGTTGCTGTACTTGCAATGAAAACAACTTGGTGGATGGTGTGTATT T C EPM2A Ensembl:ENSG00000112425 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:145686212..145686334 26863196 MeRIP-seq:(Medium) rs757199020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_819700,Human_Splice_Rec_819714,Human_Splice_Rec_819722,Human_Splice_Rec_819728,Human_Splice_Rec_819734,Human_Splice_Rec_819740,Human_Splice_Rec_819748,Human_Splice_Rec_819754,Human_Splice_Rec_819760,Human_Splice_Rec_819766,Human_Splice_Rec_819772,Human_Splice_Rec_819776,Human_Splice_Rec_819784,Human_Splice_Rec_819790,Human_Splice_Rec_819800,Human_Splice_Rec_819804,Human_Splice_Rec_819810,Human_Splice_Rec_819820,Human_Splice_Rec_819828,Human_Splice_Rec_819836,Human_Splice_Rec_819837,Human_Splice_Rec_819846,Human_Splice_Rec_819850 RMVar_hsa_circ_22324,RMVar_hsa_circ_271742,RMVar_hsa_circ_242030,RMVar_hsa_circ_242029,RMVar_hsa_circ_296751,RMVar_hsa_circ_56415 86811 RMVar_ID_86811 Human_SNP_ID_300236906 m1A Human chr6 + 145735308 145735308 145735308 CGTCCTGCGCCGCCTCCTCGGCCGCCAGCTCCACCTCCCCGAGCCACAGGCCCGGCTCCTGCAGG CGTCCTGCGCCGCCTCCTCGGCCGCCAGCTCCCCCTCCCCGAGCCACAGGCCCGGCTCCTGCAGG A C LOC100507557,LOC100507557:2 RNACentral:URS000075AF0E,RNACentral:URS0000D5C1FD lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:145735197..145735488 26863196 MeRIP-seq:(Medium) rs773140460 Functional Loss SNV dbSNP153 33..33 33 - - - 86812 RMVar_ID_86812 Human_SNP_ID_300253019 m1A Human chr6 + 145806413 145806413 145806413 GGGAATGCTGCAGCTCCTCCTCCATAATGGCCAGTCCAGCTCTGGTTGATGAAATGGAAAAAGAT GGGAATGCTGCAGCTCCTCCTCCATAATGGCCGGTCCAGCTCTGGTTGATGAAATGGAAAAAGAT A G AL356599.1 Ensembl:ENSG00000235652 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:145806326..145806425 26863196 MeRIP-seq:(Medium) rs751783937 Functional Loss SNV dbSNP153 33..33 33 - - - 86813 RMVar_ID_86813 Human_SNP_ID_300254868 m1A Human chr6 + 145814699 145814699 145814699 GCTCTGTCCCGGCGACGCTCCGTACCCCACACAGCCGTCCGAACCGCCTCCTCCGCCCCTCTTCC GCTCTGTCCCGGCGACGCTCCGTACCCCACACGGCCGTCCGAACCGCCTCCTCCGCCCCTCTTCC A G AL356599.1 Ensembl:ENSG00000235652 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:145814516..145814775 26863196 MeRIP-seq:(Medium) rs560916806 Functional Loss SNV dbSNP153 33..33 33 - - - 86814 RMVar_ID_86814 Human_SNP_ID_300430645 m1A Human chr6 + 146549484 146549484 146549484 ATTTATGTCTAGGGCAGGAGCGATTTGGCAACATGACCCGAGTATACTACAAGGAAGCTGTTGGT ATTTATGTCTAGGGCAGGAGCGATTTGGCAACGTGACCCGAGTATACTACAAGGAAGCTGTTGGT A G RAB32 Ensembl:ENSG00000118508 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:146549472..146554759 32194978 MeRIP-seq:(Medium) rs1274470530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_820422 RMVar_hsa_circ_13662,RMVar_hsa_circ_111359,RMVar_hsa_circ_83631,RMVar_hsa_circ_242067,RMVar_hsa_circ_242068 86815 RMVar_ID_86815 Human_SNP_ID_300658022 m1A Human chr6 + 147508128 147508128 147508128 TCTGGGCTGCGTACGGGATCCGAGGAAGGGGGATTCAAACGCGGATCCGGAAGGAAGGGACACTG TCTGGGCTGCGTACGGGATCCGAGGAAGGGGGTTTCAAACGCGGATCCGGAAGGAAGGGACACTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:147508078..147508252 26863196 MeRIP-seq:(Medium) rs1166599827 Functional Loss SNV dbSNP153 33..33 33 - - - 86816 RMVar_ID_86816 Human_SNP_ID_300870574 m1A Human chr6 + 148390183 148390183 148390183 CATCGATGACCTGGCGCAGCAGTATGCAGATTATTACAACACCTGTTTCTCCGACGTGTGCGAGA CATCGATGACCTGGCGCAGCAGTATGCAGATTTTTACAACACCTGTTTCTCCGACGTGTGCGAGA A T SASH1 Ensembl:ENSG00000111961 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148390097..148390203 26863196 MeRIP-seq:(Medium) rs1562373828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4868183 Human_Splice_Rec_821670,Human_Splice_Rec_821671,Human_Splice_Rec_821676,Human_Splice_Rec_821677 Human_miRNA_ID_2889900 RMVar_hsa_circ_7257,RMVar_hsa_circ_100413,RMVar_hsa_circ_299914,RMVar_hsa_circ_334986,RMVar_hsa_circ_21665,RMVar_hsa_circ_242143,RMVar_hsa_circ_242145,RMVar_hsa_circ_242146,RMVar_hsa_circ_242144 86817 RMVar_ID_86817 Human_SNP_ID_300973789 m1A Human chr6 + 148808027 148808027 148808027 GTAGGCCACGAACAGAAGCCGGTGGGGAAGCCAGGGTGGGAGGCAGGGCTGGGGCTGGTTGGGGT GTAGGCCACGAACAGAAGCCGGTGGGGAAGCCTGGGTGGGAGGCAGGGCTGGGGCTGGTTGGGGT A T UST Ensembl:ENSG00000111962 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148808023..148808089 26863196 MeRIP-seq:(Medium) rs932930783 Functional Loss SNV dbSNP153 33..33 33 - - - 86818 RMVar_ID_86818 Human_SNP_ID_300989791 m1A Human chr6 - 148877306 148877306 148877306 CCCACACTTGTACACGATACCCACACTCATACACGACCCCCCGCACTCATACACAACTCCCCGCA CCCACACTTGTACACGATACCCACACTCATACGCGACCCCCCGCACTCATACACAACTCCCCGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148877295..148877360 26863196 MeRIP-seq:(Medium) rs1186367081 Functional Loss SNV dbSNP153 33..33 33 - - - 86819 RMVar_ID_86819 Human_SNP_ID_300990012 m1A Human chr6 - 148877658 148877658 148877658 ATGACCCCCTGCACTCATACATGACCCCTCGCACTCATACACGACCCCACACTCATACACGACCC ATGACCCCCTGCACTCATACATGACCCCTCGCGCTCATACACGACCCCACACTCATACACGACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:148877580..148877703 26863196 MeRIP-seq:(Medium) rs1445962022 Functional Loss SNV dbSNP153 33..33 33 - - - 86820 RMVar_ID_86820 Human_SNP_ID_300990481 m1A Human chr6 - 148878477 148878477 148878478 ACTCATACACAATCCCTGTACTCATACACGATACCCACACTCATACACGACACCCCACTCATACA ACTCATACACAATCCCTGTACTCATACACGACCCCCACACTCATACACGACACCCCACTCATACA TA GG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148878471..148878690 26863196 MeRIP-seq:(Medium) rs796720027 Functional Loss MNV dbSNP153 32..33 33 - - - 86821 RMVar_ID_86821 Human_SNP_ID_300990482 m1A Human chr6 - 148878477 148878477 148878477 ACTCATACACAATCCCTGTACTCATACACGATACCCACACTCATACACGACACCCCACTCATACA ACTCATACACAATCCCTGTACTCATACACGATCCCCACACTCATACACGACACCCCACTCATACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148878471..148878690 26863196 MeRIP-seq:(Medium) rs1008600260 Functional Loss SNV dbSNP153 33..33 33 - - - 86822 RMVar_ID_86822 Human_SNP_ID_300990546 m1A Human chr6 - 148878612 148878593 148878612 ACTCATACACGATCTCCACACTCATACACGACACCCACACTAATACACGACCCCCGCACTCATAC ACTCATACACGATCTCCACACTCATACACGAC___________________CCCCGCACTCATAC GGTCGTGTATTAGTGTGGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:148878593..148878720 26863196 MeRIP-seq:(Medium) rs1364823096 Functional Loss DEL dbSNP153 33..51 33 - - - 86823 RMVar_ID_86823 Human_SNP_ID_300990551 m1A Human chr6 - 148878621 148878603 148878622 ACCCCCCGCACTCATACACGATCTCCACACTCATACACGACACCCACACTAATACACGACCCCCG ACCCCCCGCACTCATACACGATCTCCACACT___________________AATACACGACCCCCG TAGTGTGGGTGTCGTGTATG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:148878601..148878691 26863196 MeRIP-seq:(Medium) rs1562286645 Functional Loss DEL dbSNP153 32..50 33 - - - 86824 RMVar_ID_86824 Human_SNP_ID_300990555 m1A Human chr6 - 148878612 148878605 148878612 ACTCATACACGATCTCCACACTCATACACGACACCCACACTAATACACGACCCCCGCACTCATAC ACTCATACACGATCTCCACACTCATACACGAC_______CTAATACACGACCCCCGCACTCATAC GTGTGGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:148878593..148878720 26863196 MeRIP-seq:(Medium) rs1437430092 Functional Loss DEL dbSNP153 33..39 33 - - - 86825 RMVar_ID_86825 Human_SNP_ID_300990558 m1A Human chr6 - 148878612 148878612 148878612 ACTCATACACGATCTCCACACTCATACACGACACCCACACTAATACACGACCCCCGCACTCATAC ACTCATACACGATCTCCACACTCATACACGACCCCCACACTAATACACGACCCCCGCACTCATAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:148878593..148878720 26863196 MeRIP-seq:(Medium) rs1279137921 Functional Loss SNV dbSNP153 33..33 33 - - - 86826 RMVar_ID_86826 Human_SNP_ID_301025977 m1A Human chr6 + 149032164 149032164 149032164 GTGGCGCAACCTGGCACTGAGTCACTCATACCAATCTCAGCGCCAGTGGCCAAGCCGCTGCTGCC GTGGCGCAACCTGGCACTGAGTCACTCATACCGATCTCAGCGCCAGTGGCCAAGCCGCTGCTGCC A G UST Ensembl:ENSG00000111962 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:149032123..149032255 26863196 MeRIP-seq:(Medium) rs1009096371 Functional Loss SNV dbSNP153 33..33 33 - - - 86827 RMVar_ID_86827 Human_SNP_ID_301026094 m1A Human chr6 - 149032579 149032579 149032579 GAAGAAGGCCAGGAAGAGCAGAGGATGGTGCCAGGAGGATGATGTCGGGGGACACAGGCAGCTCA GAAGAAGGCCAGGAAGAGCAGAGGATGGTGCCGGGAGGATGATGTCGGGGGACACAGGCAGCTCA T C LOC105378047 RNACentral:URS0000A776CA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149032392..149032646 26863196 MeRIP-seq:(Medium) rs1285409930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_821787 86828 RMVar_ID_86828 Human_SNP_ID_301093189 m1A Human chr6 + 149317699 149317699 149317699 AGCGAGCCGGAGCTGAGGATTGGGGAGCGGCGACGCCGCCCAGCCGTCGTTTTTGATCTGCTGCA AGCGAGCCGGAGCTGAGGATTGGGGAGCGGCGCCGCCGCCCAGCCGTCGTTTTTGATCTGCTGCA A C TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:149317655..149317963 26863196 MeRIP-seq:(Medium) rs969874153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791889,Human_RBP_ID_840734,Human_RBP_ID_3820930,Human_RBP_ID_4903544,Human_RBP_ID_5151979,Human_RBP_ID_5217417,Human_RBP_ID_5327550,Human_RBP_ID_7556661,Human_RBP_ID_8143659,Human_RBP_ID_8215368,Human_RBP_ID_8237150,Human_RBP_ID_8944083,Human_RBP_ID_9437571,Human_RBP_ID_17309245,Human_RBP_ID_17421878,Human_RBP_ID_18425506,Human_RBP_ID_18465620,Human_RBP_ID_18957738,Human_RBP_ID_21991177,Human_RBP_ID_26354500,Human_RBP_ID_26792514 86829 RMVar_ID_86829 Human_SNP_ID_301093202 m1A Human chr6 + 149317731 149317731 149317731 ACGCCGCCCAGCCGTCGTTTTTGATCTGCTGCAGCCGCCGGCGGGGCGACCCAGCCCGACCCCCT ACGCCGCCCAGCCGTCGTTTTTGATCTGCTGCCGCCGCCGGCGGGGCGACCCAGCCCGACCCCCT A C TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:149317643..149317730 26863410 MeRIP-seq:(Medium) rs1325025525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3820930,Human_RBP_ID_4903545,Human_RBP_ID_5151980,Human_RBP_ID_5217252,Human_RBP_ID_5242595,Human_RBP_ID_5327550,Human_RBP_ID_8215368,Human_RBP_ID_8237535,Human_RBP_ID_9438538,Human_RBP_ID_18066820,Human_RBP_ID_18425506,Human_RBP_ID_21991177,Human_RBP_ID_22106959,Human_RBP_ID_24140118 86830 RMVar_ID_86830 Human_SNP_ID_301093203 m1A Human chr6 + 149317731 149317731 149317731 ACGCCGCCCAGCCGTCGTTTTTGATCTGCTGCAGCCGCCGGCGGGGCGACCCAGCCCGACCCCCT ACGCCGCCCAGCCGTCGTTTTTGATCTGCTGCGGCCGCCGGCGGGGCGACCCAGCCCGACCCCCT A G TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:149317643..149317730 26863410 MeRIP-seq:(Medium) rs1325025525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3820930,Human_RBP_ID_4903545,Human_RBP_ID_5151980,Human_RBP_ID_5217252,Human_RBP_ID_5242595,Human_RBP_ID_5327550,Human_RBP_ID_8215368,Human_RBP_ID_8237535,Human_RBP_ID_9438538,Human_RBP_ID_18066820,Human_RBP_ID_18425506,Human_RBP_ID_21991177,Human_RBP_ID_22106959,Human_RBP_ID_24140118 86831 RMVar_ID_86831 Human_SNP_ID_301093260 m1A Human chr6 + 149317854 149317854 149317854 GCGGGCGAGCGGAGGGGGCTGAGCGGGGAGGGAGGGAGGGCTGAGGTGTCCCCCCTGCCGGGTGG GCGGGCGAGCGGAGGGGGCTGAGCGGGGAGGGGGGGAGGGCTGAGGTGTCCCCCCTGCCGGGTGG A G TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:149317632..149318020 26863196 MeRIP-seq:(Medium) rs914353998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3820931,Human_RBP_ID_4903546,Human_RBP_ID_5151981,Human_RBP_ID_5327551,Human_RBP_ID_5401193,Human_RBP_ID_8216219,Human_RBP_ID_8237151,Human_RBP_ID_9336318,Human_RBP_ID_9437572,Human_RBP_ID_17421879,Human_RBP_ID_17663486,Human_RBP_ID_17671972,Human_RBP_ID_22106197,Human_RBP_ID_22461463,Human_RBP_ID_26792515 86832 RMVar_ID_86832 Human_SNP_ID_301093279 m1A Human chr6 + 149317888 149317888 149317888 GGAGGGCTGAGGTGTCCCCCCTGCCGGGTGGAACCGGAGGCGGCGGCGGCGCTGGCGGCGGCCGT GGAGGGCTGAGGTGTCCCCCCTGCCGGGTGGATCCGGAGGCGGCGGCGGCGCTGGCGGCGGCCGT A T TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:149317645..149318610 26863196 MeRIP-seq:(Medium) rs968197350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251955,Human_RBP_ID_654973,Human_RBP_ID_3820931,Human_RBP_ID_4903546,Human_RBP_ID_5151981,Human_RBP_ID_5327551,Human_RBP_ID_8216219,Human_RBP_ID_8237151,Human_RBP_ID_8944037,Human_RBP_ID_9336318,Human_RBP_ID_9437572,Human_RBP_ID_17421879,Human_RBP_ID_17663486,Human_RBP_ID_17671972,Human_RBP_ID_22105447,Human_RBP_ID_22461463,Human_RBP_ID_26792515 86833 RMVar_ID_86833 Human_SNP_ID_301106005 m1A Human chr6 + 149369839 149369839 149369839 TAAGTGCTAAAGCACATATTCTTTTGTACTGAAATTTTAAATCCACAACAATATTCCTTCTATAA TAAGTGCTAAAGCACATATTCTTTTGTACTGAGATTTTAAATCCACAACAATATTCCTTCTATAA A G TAB2 Ensembl:ENSG00000055208 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149369837..149370039 26863196 MeRIP-seq:(Medium) rs887232396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_271885,RMVar_hsa_circ_277314,RMVar_hsa_circ_242176,RMVar_hsa_circ_242177 86834 RMVar_ID_86834 Human_SNP_ID_301108283 m1A Human chr6 + 149378950 149378950 149378950 AGAAATAATTCTTCAAAACTGCGTTCTTCTGGACCTCGAACCTCCAGCACTTCCTCTTCAGTCAA AGAAATAATTCTTCAAAACTGCGTTCTTCTGGGCCTCGAACCTCCAGCACTTCCTCTTCAGTCAA A G TAB2 Ensembl:ENSG00000055208 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:149378899..149379077 26863196 MeRIP-seq:(Medium) rs923428062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3797001,Human_RBP_ID_8897262,Human_RBP_ID_17305048,Human_RBP_ID_17418424,Human_RBP_ID_17534135 Human_miRNA_ID_2315182,Human_miRNA_ID_2318342,Human_miRNA_ID_2321499,Human_miRNA_ID_2324657,Human_miRNA_ID_2519037,Human_miRNA_ID_2522206,Human_miRNA_ID_2774047,Human_miRNA_ID_2821402,Human_miRNA_ID_2827532,Human_miRNA_ID_2830684,Human_miRNA_ID_2834803,Human_miRNA_ID_2840166 RMVar_hsa_circ_456,RMVar_hsa_circ_277314,RMVar_hsa_circ_242177,RMVar_hsa_circ_309788,RMVar_hsa_circ_242179,RMVar_hsa_circ_242180,RMVar_hsa_circ_279485 86835 RMVar_ID_86835 Human_SNP_ID_301126672 m1A Human chr6 - 149451386 149451386 149451386 GCAACTGGCGGTGGCCGACGAGCTCCGCGCCAAGACAGGGGCCCGGCCTGGCGCGGGCGCCGAGG GCAACTGGCGGTGGCCGACGAGCTCCGCGCCAGGACAGGGGCCCGGCCTGGCGCGGGCGCCGAGG T C ZC3H12D Ensembl:ENSG00000178199 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149451340..149451427 26863196 MeRIP-seq:(Medium) rs1417096889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_821904 RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 86836 RMVar_ID_86836 Human_SNP_ID_301149543 m1A Human chr6 - 149545994 149545994 149545994 AGCGGAGGAGGAGCGGGCGCCATGGCGGTTCTACTGGAGACCACTTTAGGCGACGTCGTCATCGA AGCGGAGGAGGAGCGGGCGCCATGGCGGTTCTGCTGGAGACCACTTTAGGCGACGTCGTCATCGA T C PPIL4 Ensembl:ENSG00000131013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149545904..149546012 26863196 MeRIP-seq:(Medium) rs373364423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792158,Human_RBP_ID_1665489,Human_RBP_ID_4868496,Human_RBP_ID_7557721,Human_RBP_ID_8905539,Human_RBP_ID_9309426,Human_RBP_ID_15681418,Human_RBP_ID_22105449,Human_RBP_ID_22306461 Human_Splice_Rec_821919 86837 RMVar_ID_86837 Human_SNP_ID_301149544 m1A Human chr6 - 149545994 149545994 149545994 AGCGGAGGAGGAGCGGGCGCCATGGCGGTTCTACTGGAGACCACTTTAGGCGACGTCGTCATCGA AGCGGAGGAGGAGCGGGCGCCATGGCGGTTCTCCTGGAGACCACTTTAGGCGACGTCGTCATCGA T G PPIL4 Ensembl:ENSG00000131013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149545904..149546012 26863196 MeRIP-seq:(Medium) rs373364423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792158,Human_RBP_ID_1665489,Human_RBP_ID_4868496,Human_RBP_ID_7557721,Human_RBP_ID_8905539,Human_RBP_ID_9309426,Human_RBP_ID_15681418,Human_RBP_ID_22105449,Human_RBP_ID_22306461 Human_Splice_Rec_821919 86838 RMVar_ID_86838 Human_SNP_ID_301157740 m1A Human chr6 + 149577444 149577442 149577445 CACTAGAGAGAGGAGCAGCGAGGGGCCAGATGAGGAGCCTGAGGAGGACCAGTGAGAGGACCGGG CACTAGAGAGAGGAGCAGCGAGGGGCCAGAT___GAGCCTGAGGAGGACCAGTGAGAGGACCGGG TGAG T GINM1 Ensembl:ENSG00000055211 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149577431..149577556 26863196 MeRIP-seq:(Medium) rs1216241036 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_7557761,Human_RBP_ID_15681636 RMVar_hsa_circ_93173,RMVar_hsa_circ_271899,RMVar_hsa_circ_335850,RMVar_hsa_circ_97233,RMVar_hsa_circ_102891,RMVar_hsa_circ_242200,RMVar_hsa_circ_242202,RMVar_hsa_circ_242203,RMVar_hsa_circ_242204,RMVar_hsa_circ_242201,RMVar_hsa_circ_242205 86839 RMVar_ID_86839 Human_SNP_ID_301194240 m1A Human chr6 - 149724612 149724612 149724612 GCCACTTCACTCCAGCCTGGGCAAAAGAGCAAAACGCCATCTCAAAAAATATACATATATAAGGA GCCACTTCACTCCAGCCTGGGCAAAAGAGCAAGACGCCATCTCAAAAAATATACATATATAAGGA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242237,RMVar_hsa_circ_104444,RMVar_hsa_circ_126820,RMVar_hsa_circ_125789,RMVar_hsa_circ_242235,RMVar_hsa_circ_377038,RMVar_hsa_circ_120261,RMVar_hsa_circ_77971,RMVar_hsa_circ_93960,RMVar_hsa_circ_242239,RMVar_hsa_circ_242240,RMVar_hsa_circ_242241,RMVar_hsa_circ_242238,RMVar_hsa_circ_242236 86840 RMVar_ID_86840 Human_SNP_ID_301194260 m1A Human chr6 - 149724682 149724682 149724682 CTACTTGGGAGGCTGAGGCAGGAGAATTGCTCAAACCCGGGAGGCAGAGGTTGCAGTGACCCAAG CTACTTGGGAGGCTGAGGCAGGAGAATTGCTCGAACCCGGGAGGCAGAGGTTGCAGTGACCCAAG T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3177640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22728415 RMVar_hsa_circ_242237,RMVar_hsa_circ_104444,RMVar_hsa_circ_126820,RMVar_hsa_circ_125789,RMVar_hsa_circ_242235,RMVar_hsa_circ_377038,RMVar_hsa_circ_120261,RMVar_hsa_circ_77971,RMVar_hsa_circ_93960,RMVar_hsa_circ_242239,RMVar_hsa_circ_242240,RMVar_hsa_circ_242241,RMVar_hsa_circ_242238,RMVar_hsa_circ_242236 86841 RMVar_ID_86841 Human_SNP_ID_301194294 m1A Human chr6 - 149724792 149724792 149724792 CTGAGGTCAAGAGTTCGAGATCAGCCTGGCCAACATGGCGAAACCCCGTCTCCACTAAAAATGCA CTGAGGTCAAGAGTTCGAGATCAGCCTGGCCAGCATGGCGAAACCCCGTCTCCACTAAAAATGCA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1129792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242237,RMVar_hsa_circ_104444,RMVar_hsa_circ_126820,RMVar_hsa_circ_125789,RMVar_hsa_circ_242235,RMVar_hsa_circ_377038,RMVar_hsa_circ_120261,RMVar_hsa_circ_77971,RMVar_hsa_circ_93960,RMVar_hsa_circ_242239,RMVar_hsa_circ_242240,RMVar_hsa_circ_242241,RMVar_hsa_circ_242238,RMVar_hsa_circ_242236 86842 RMVar_ID_86842 Human_SNP_ID_301195232 m1A Human chr6 - 149728761 149728761 149728761 CAGCAAATGCTGAGGGCCTGAGACAGGCAGAGAACTGCAAGGACACCACGGTTGGAGCTCAGGCA CAGCAAATGCTGAGGGCCTGAGACAGGCAGAGCACTGCAAGGACACCACGGTTGGAGCTCAGGCA T G NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149728710..149728959 26863196 MeRIP-seq:(Medium) rs1384821097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_655334,Human_RBP_ID_15683589,Human_RBP_ID_24140693 RMVar_hsa_circ_242237,RMVar_hsa_circ_104444,RMVar_hsa_circ_126820,RMVar_hsa_circ_125789,RMVar_hsa_circ_242235,RMVar_hsa_circ_377038,RMVar_hsa_circ_120261,RMVar_hsa_circ_77971,RMVar_hsa_circ_93960,RMVar_hsa_circ_242239,RMVar_hsa_circ_242240,RMVar_hsa_circ_242241,RMVar_hsa_circ_242238,RMVar_hsa_circ_242236 86843 RMVar_ID_86843 Human_SNP_ID_301195439 m1A Human chr6 + 149729663 149729663 149729663 CTATTACCTTTTGTTTTCCCAGCCCTTCTAACACATGTGAGACCAATTCCTTCTACATCTAAGGT CTATTACCTTTTGTTTTCCCAGCCCTTCTAACGCATGTGAGACCAATTCCTTCTACATCTAAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149729613..149729682 26863196 MeRIP-seq:(Medium) rs1038671425 Functional Loss SNV dbSNP153 33..33 33 - - - 86844 RMVar_ID_86844 Human_SNP_ID_301201213 m1A Human chr6 + 149749779 149749779 149749779 GCGGCAGCGGCGGCGACGGCAGTAACAGCGGCAGCTACAGCGGGGACGCGAGCGGGGCGGTGACG GCGGCAGCGGCGGCGACGGCAGTAACAGCGGCGGCTACAGCGGGGACGCGAGCGGGGCGGTGACG A G PCMT1 Ensembl:ENSG00000120265 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:149749722..149749925;chr6:149749726..149749940;chr6:149749726..149749900 26863196 MeRIP-seq:(Medium) rs1444865712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251399,Human_RBP_ID_655349,Human_RBP_ID_841419,Human_RBP_ID_4903550,Human_RBP_ID_9336321,Human_RBP_ID_22461465,Human_RBP_ID_22829780,Human_RBP_ID_27089443 RMVar_hsa_circ_119973,RMVar_hsa_circ_242250 86845 RMVar_ID_86845 Human_SNP_ID_301201259 m1A Human chr6 + 149749866 149749866 149749866 TGGGAAAACTGCTGGGCACCGTCGTCGCGCTGAAGGTGGTTCTGTACCTGCTCCGAGTGTGCTTA TGGGAAAACTGCTGGGCACCGTCGTCGCGCTGCAGGTGGTTCTGTACCTGCTCCGAGTGTGCTTA A C PCMT1 Ensembl:ENSG00000120265 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs539885843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_655350,Human_RBP_ID_841421,Human_RBP_ID_951247,Human_RBP_ID_1665642,Human_RBP_ID_2011260,Human_RBP_ID_3797324,Human_RBP_ID_4868814,Human_RBP_ID_5427958,Human_RBP_ID_5477478,Human_RBP_ID_5510662,Human_RBP_ID_7558517,Human_RBP_ID_8634144,Human_RBP_ID_8897419,Human_RBP_ID_9336321,Human_RBP_ID_15684006,Human_RBP_ID_17671924,Human_RBP_ID_18856408,Human_RBP_ID_22306584,Human_RBP_ID_22461465,Human_RBP_ID_23137691,Human_RBP_ID_27341727,Human_RBP_ID_27520232 Human_Splice_Rec_822219,Human_Splice_Rec_822233,Human_Splice_Rec_822245,Human_Splice_Rec_822257,Human_Splice_Rec_822271,Human_Splice_Rec_822285,Human_Splice_Rec_822297,Human_Splice_Rec_822309,Human_Splice_Rec_822315,Human_Splice_Rec_822323 RMVar_hsa_circ_119973,RMVar_hsa_circ_242250 86846 RMVar_ID_86846 Human_SNP_ID_301225048 m1A Human chr6 - 149842477 149842477 149842477 CCGGAGGAACAGGTTCTGGTGATCTGTTGCACAGCATGGTGACTATAGTTAATGATAATGTATTG CCGGAGGAACAGGTTCTGGTGATCTGTTGCACGGCATGGTGACTATAGTTAATGATAATGTATTG T C AL355312.6,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000120256 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149842475..149842674 26863196 MeRIP-seq:(Medium) rs1308495180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98949,RMVar_hsa_circ_275224,RMVar_hsa_circ_242272,RMVar_hsa_circ_293819,RMVar_hsa_circ_242275,RMVar_hsa_circ_242276,RMVar_hsa_circ_242281,RMVar_hsa_circ_242279,RMVar_hsa_circ_340788,RMVar_hsa_circ_272835,RMVar_hsa_circ_83499,RMVar_hsa_circ_298250,RMVar_hsa_circ_242280 86847 RMVar_ID_86847 Human_SNP_ID_301225261 m1A Human chr6 + 149843123 149843123 149843123 GGTGGGACAGCTTCAGGGTTCCTGATTGAGGCACCTGCCACACAGATGGGACACATCACGTCGAG GGTGGGACAGCTTCAGGGTTCCTGATTGAGGCCCCTGCCACACAGATGGGACACATCACGTCGAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:149843103..149864219 32194978 MeRIP-seq:(Medium) rs201369161 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 86848 RMVar_ID_86848 Human_SNP_ID_301230243 m1A Human chr6 + 149863551 149863547 149863551 GCGCCGTGCAGTTGAAGAGGTAGCAGCCGAGCACGGCTGCCGGGGGCGCGGGGCGCCGGGGCAGC GCGCCGTGCAGTTGAAGAGGTAGCAGCCG____CGGCTGCCGGGGGCGCGGGGCGCCGGGGCAGC GAGCA G AL355312.3 Ensembl:ENSG00000268592 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149863502..149863606 26863196 MeRIP-seq:(Medium) rs957812597 Functional Loss DEL dbSNP153 30..33 33 - - - 86849 RMVar_ID_86849 Human_SNP_ID_301230497 m1A Human chr6 + 149864049 149864049 149864049 CCATGGCGACGAGAGCCAAGGGCAGCGAGCCGAGGCGGGGCTGAGCGCGGGAGGAAGGCGGGGAC CCATGGCGACGAGAGCCAAGGGCAGCGAGCCGGGGCGGGGCTGAGCGCGGGAGGAAGGCGGGGAC A G AL355312.3 Ensembl:ENSG00000268592 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:149864001..149864350 26863196 MeRIP-seq:(Medium) rs1458790672 Functional Loss SNV dbSNP153 33..33 33 - - - 86850 RMVar_ID_86850 Human_SNP_ID_301230586 m1A Human chr6 - 149864295 149864295 149864295 CGAGGCCGACTCGTCGCCACCCAGCGCGCCGCAGGCCGGGGCGGAGAGGCGCAGGGCGCTGGGCA CGAGGCCGACTCGTCGCCACCCAGCGCGCCGCGGGCCGGGGCGGAGAGGCGCAGGGCGCTGGGCA T C AL355312.6,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000120256 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:149864191..149864325;chr6:149863407..149864350;chr6:149863918..149864350 26863196 MeRIP-seq:(Medium) rs1417577123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252814,Human_RBP_ID_842154 RMVar_hsa_circ_242281,RMVar_hsa_circ_83499 86851 RMVar_ID_86851 Human_SNP_ID_301235087 m1A Human chr6 - 149884003 149884003 149884003 GGAAATTGGGGGAATTAAACAGAGGGGAGGGCATGGATCCCCGGGAGTTAGAAGAGTAGCAGCTT GGAAATTGGGGGAATTAAACAGAGGGGAGGGCGTGGATCCCCGGGAGTTAGAAGAGTAGCAGCTT T C AL355312.6,RAET1E Ensembl:ENSG00000285991,Ensembl:ENSG00000164520 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:149883954..149884111 26863196 MeRIP-seq:(Medium) rs1429702353 Functional Loss SNV dbSNP153 33..33 33 - - - 86852 RMVar_ID_86852 Human_SNP_ID_301235090 m1A Human chr6 - 149884008 149884008 149884008 TAAGAGGAAATTGGGGGAATTAAACAGAGGGGAGGGCATGGATCCCCGGGAGTTAGAAGAGTAGC TAAGAGGAAATTGGGGGAATTAAACAGAGGGGTGGGCATGGATCCCCGGGAGTTAGAAGAGTAGC T A AL355312.6,RAET1E Ensembl:ENSG00000285991,Ensembl:ENSG00000164520 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149883959..149884090 26863196 MeRIP-seq:(Medium) rs377757685 Functional Loss SNV dbSNP153 33..33 33 - - - 86853 RMVar_ID_86853 Human_SNP_ID_301235100 m1A Human chr6 - 149884055 149884055 149884055 AGGGAGAAAAGAGAGATAAGCAAAGAACAGAGAGGAAAAATGGAAAATAAGAGGAAATTGGGGGA AGGGAGAAAAGAGAGATAAGCAAAGAACAGAGGGGAAAAATGGAAAATAAGAGGAAATTGGGGGA T C AL355312.6,RAET1E Ensembl:ENSG00000285991,Ensembl:ENSG00000164520 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149883966..149884098 26863196 MeRIP-seq:(Medium) rs1206101342 Functional Loss SNV dbSNP153 33..33 33 - - - 86854 RMVar_ID_86854 Human_SNP_ID_301244886 m1A Human chr6 - 149923019 149923019 149923019 CTGGGCTTCGCTTCTGCTGTCCCCTGCGATCCAACTCCCCAATGGCAGCGGCCGCCAGCCCCGCG CTGGGCTTCGCTTCTGCTGTCCCCTGCGATCCGACTCCCCAATGGCAGCGGCCGCCAGCCCCGCG T C RAET1G Ensembl:ENSG00000203722 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:149922970..149923071 26863196 MeRIP-seq:(Medium) rs1238715653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_822447,Human_Splice_Rec_822455,Human_Splice_Rec_822463 86855 RMVar_ID_86855 Human_SNP_ID_301250090 m1A Human chr6 - 149942061 149942061 149942061 GGTAGCGGCGGCTGCTGCCATTAAGGACCCAGAGCGCTAGGGATGAGAGACTTGATGGAAGGAGA GGTAGCGGCGGCTGCTGCCATTAAGGACCCAGGGCGCTAGGGATGAGAGACTTGATGGAAGGAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149941993..149942189 26863196 MeRIP-seq:(Medium) rs1417900819 Functional Loss SNV dbSNP153 33..33 33 - - - 86856 RMVar_ID_86856 Human_SNP_ID_301251055 m1A Human chr6 - 149945261 149945261 149945261 GGTGAGGGGTGGGTGGGGAGGAAAAGACCCCTAGTTAGCCCCCCTCCACGCTGTGTCAATAAGAG GGTGAGGGGTGGGTGGGGAGGAAAAGACCCCTGGTTAGCCCCCCTCCACGCTGTGTCAATAAGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149945257..149945323 26863196 MeRIP-seq:(Medium) rs1234846965 Functional Loss SNV dbSNP153 33..33 33 - - - 86857 RMVar_ID_86857 Human_SNP_ID_301256750 m1A Human chr6 - 149964023 149964023 149964023 TGCCATTGTAGACCTGGAGCTCCGTGGACAGGAGGCGCTGATGGTTCCCTTCGAGGCTCACACCA TGCCATTGTAGACCTGGAGCTCCGTGGACAGGTGGCGCTGATGGTTCCCTTCGAGGCTCACACCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:149963996..149964071 26863196 MeRIP-seq:(Medium) rs1374707237 Functional Loss SNV dbSNP153 33..33 33 - - - 86858 RMVar_ID_86858 Human_SNP_ID_301257138 m1A Human chr6 - 149964842 149964842 149964842 GGGGGGACCGCGATGTTCGGGGAGACCGCGTTACTCGGGGGGACGGCGATGTTCGGGGGGGATCA GGGGGGACCGCGATGTTCGGGGAGACCGCGTTGCTCGGGGGGACGGCGATGTTCGGGGGGGATCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:149964840..149964939 26863196 MeRIP-seq:(Medium) rs1435617417 Functional Loss SNV dbSNP153 33..33 33 - - - 86859 RMVar_ID_86859 Human_SNP_ID_301257158 m1A Human chr6 - 149964886 149964869 149964887 CAATGTACGGGGAGACGGCGATGTTCGGGGGTACCGCGATGTTCGGGGGGACCGCGATGTTCGGG CAATGTACGGGGAGACGGCGATGTTCGGGGG__________________GACCGCGATGTTCGGG CCCCCCGAACATCGCGGTA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:149964789..149964972 26863196 MeRIP-seq:(Medium) rs1472625814 Functional Loss DEL dbSNP153 32..49 33 - - - 86860 RMVar_ID_86860 Human_SNP_ID_361828670 m1A Human chr8 + 46829103 46829103 46829103 GAACACTCATGTGGCCATTCATACAAGTCCCTATTTGCGGAACAAGTGATTATTCTACCTTTGCA GAACACTCATGTGGCCATTCATACAAGTCCCTGTTTGCGGAACAAGTGATTATTCTACCTTTGCA A G LINC00293 Ensembl:ENSG00000253314 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:46829053..46829228 26863196 MeRIP-seq:(Medium) rs1258833242 Functional Loss SNV dbSNP153 33..33 33 - - - 86861 RMVar_ID_86861 Human_SNP_ID_361828679 m1A Human chr8 + 46829135 46829135 46829135 ATTTGCGGAACAAGTGATTATTCTACCTTTGCACTGTCAGGATACTGCGGCCATTGAACATATGT ATTTGCGGAACAAGTGATTATTCTACCTTTGCGCTGTCAGGATACTGCGGCCATTGAACATATGT A G LINC00293 Ensembl:ENSG00000253314 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:46829034..46829217 26863196 MeRIP-seq:(Medium) rs1397185011 Functional Loss SNV dbSNP153 33..33 33 - - - 86862 RMVar_ID_86862 Human_SNP_ID_361976471 m1A Human chr8 + 47398724 47398724 47398724 GAATGCGTAGACTGCAGTGTCCAGATCTTTTGAAGCATGAGCTAGGTCAGGTCACAGGAGATCCA GAATGCGTAGACTGCAGTGTCCAGATCTTTTGGAGCATGAGCTAGGTCAGGTCACAGGAGATCCA A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:47398720..47398984 26863196 MeRIP-seq:(Medium) rs1160629256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2664,RMVar_hsa_circ_13332,RMVar_hsa_circ_50885,RMVar_hsa_circ_302842,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_62226,RMVar_hsa_circ_45941,RMVar_hsa_circ_288740,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_291502,RMVar_hsa_circ_33506,RMVar_hsa_circ_40623,RMVar_hsa_circ_357413,RMVar_hsa_circ_334257,RMVar_hsa_circ_331439,RMVar_hsa_circ_318136,RMVar_hsa_circ_365661,RMVar_hsa_circ_73193,RMVar_hsa_circ_276139,RMVar_hsa_circ_288442,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895 86863 RMVar_ID_86863 Human_SNP_ID_361976479 m1A Human chr8 + 47398752 47398752 47398752 TTTGAAGCATGAGCTAGGTCAGGTCACAGGAGATCCAGTGCTGGGCGAGAGGAGAACCTGTCCAA TTTGAAGCATGAGCTAGGTCAGGTCACAGGAGTTCCAGTGCTGGGCGAGAGGAGAACCTGTCCAA A T SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:47398733..47398983 26863196 MeRIP-seq:(Medium) rs567482193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18390973 RMVar_hsa_circ_2664,RMVar_hsa_circ_13332,RMVar_hsa_circ_50885,RMVar_hsa_circ_302842,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_62226,RMVar_hsa_circ_45941,RMVar_hsa_circ_288740,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_291502,RMVar_hsa_circ_33506,RMVar_hsa_circ_40623,RMVar_hsa_circ_357413,RMVar_hsa_circ_334257,RMVar_hsa_circ_331439,RMVar_hsa_circ_318136,RMVar_hsa_circ_365661,RMVar_hsa_circ_73193,RMVar_hsa_circ_276139,RMVar_hsa_circ_288442,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895 86864 RMVar_ID_86864 Human_SNP_ID_361990255 m1A Human chr8 - 47449083 47449083 47449083 ATAGTCCAAAGCACCACCTTTTTCCACACTTGAGCTACTCCCACAGCCTCCGAGATGCATTTATT ATAGTCCAAAGCACCACCTTTTTCCACACTTGGGCTACTCCCACAGCCTCCGAGATGCATTTATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:47449063..47449161 26863196 MeRIP-seq:(Medium) rs1186631676 Functional Loss SNV dbSNP153 33..33 33 - - - 86865 RMVar_ID_86865 Human_SNP_ID_362056947 m1A Human chr8 - 47714097 47714097 47714097 CCTGGTGGGCCCACCAGCCTCAGCTTGGTCCCACCTCCATCTGGCTGCCTGTCCTGCCTCTTCCC CCTGGTGGGCCCACCAGCCTCAGCTTGGTCCCGCCTCCATCTGGCTGCCTGTCCTGCCTCTTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:47713978..47714241 26863196 MeRIP-seq:(Medium) rs1349638508 Functional Loss SNV dbSNP153 33..33 33 - - - 86866 RMVar_ID_86866 Human_SNP_ID_362062645 m1A Human chr8 - 47737246 47737246 47737246 ACCCATACCTCAGACCCGACGGCCCGGAGCGGAGCGCGCCCTGCCCTGGCGCAGCCAGAGCCGCC ACCCATACCTCAGACCCGACGGCCCGGAGCGGCGCGCGCCCTGCCCTGGCGCAGCCAGAGCCGCC T G CEBPD Ensembl:ENSG00000221869 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47737199..47737308 26863196 MeRIP-seq:(Medium) rs1230956761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264863 86867 RMVar_ID_86867 Human_SNP_ID_362062695 m1A Human chr8 - 47737355 47737355 47737355 CCGGCCTCCGGCAGTTCTTCAAGCAGCTGCCCAGCCCGCCCTTCCTGCCGGCCGCCGGGACAGCA CCGGCCTCCGGCAGTTCTTCAAGCAGCTGCCCGGCCCGCCCTTCCTGCCGGCCGCCGGGACAGCA T C CEBPD Ensembl:ENSG00000221869 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47737304..47738096 32194978 MeRIP-seq:(Medium) rs752703091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22114995 RMVar_hsa_circ_264863 86868 RMVar_ID_86868 Human_SNP_ID_362062696 m1A Human chr8 - 47737355 47737355 47737355 CCGGCCTCCGGCAGTTCTTCAAGCAGCTGCCCAGCCCGCCCTTCCTGCCGGCCGCCGGGACAGCA CCGGCCTCCGGCAGTTCTTCAAGCAGCTGCCCCGCCCGCCCTTCCTGCCGGCCGCCGGGACAGCA T G CEBPD Ensembl:ENSG00000221869 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47737304..47738096 32194978 MeRIP-seq:(Medium) rs752703091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22114995 RMVar_hsa_circ_264863 86869 RMVar_ID_86869 Human_SNP_ID_362062775 m1A Human chr8 - 47737502 47737502 47737502 AGCGGCGCGAGCGCAACAACATCGCCGTGCGCAAGAGCCGCGACAAGGCCAAGCGGCGCAACCAG AGCGGCGCGAGCGCAACAACATCGCCGTGCGCTAGAGCCGCGACAAGGCCAAGCGGCGCAACCAG T A CEBPD Ensembl:ENSG00000221869 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47737452..47737552 32194978 MeRIP-seq:(Medium) rs371024952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264863 86870 RMVar_ID_86870 Human_SNP_ID_362062979 m1A Human chr8 - 47737937 47737937 47737937 CCATGTACGACGACGAGAGCGCCATCGACTTCAGCGCCTACATCGACTCCATGGCCGCCGTGCCC CCATGTACGACGACGAGAGCGCCATCGACTTCCGCGCCTACATCGACTCCATGGCCGCCGTGCCC T G CEBPD Ensembl:ENSG00000221869 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:47737818..47738066 26863196 MeRIP-seq:(Medium) rs1339334572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264863 86871 RMVar_ID_86871 Human_SNP_ID_362063002 m1A Human chr8 + 47737996 47737979 47737997 ACATGGCGGGGGCGGCGGCGCCTGGCTCGCCTAGGGCCCCTGGCTCGGCCCCGCGGCCCGGCTTG ACATGGCGGGGGCGGC__________________GGCCCCTGGCTCGGCCCCGCGGCCCGGCTTG CGGCGCCTGGCTCGCCTAG C RF00017-4500,RF00017-4520 RNACentral:URS000099DB47,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47737947..47738096 32194978 MeRIP-seq:(Medium) rs748648042 Functional Loss DEL dbSNP153 17..34 33 - - - 86872 RMVar_ID_86872 Human_SNP_ID_362075439 m1A Human chr8 + 47783728 47783728 47783728 GAACGTTCATCAGGACAGGGACTGGGTCACACACCCTCACACCTACCCGCTCATCAAACCCGGCG GAACGTTCATCAGGACAGGGACTGGGTCACACCCCCTCACACCTACCCGCTCATCAAACCCGGCG A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47783726..47783800 32194978 MeRIP-seq:(Medium) rs764415768 Functional Loss SNV dbSNP153 33..33 33 - - - 86873 RMVar_ID_86873 Human_SNP_ID_362075440 m1A Human chr8 + 47783728 47783728 47783728 GAACGTTCATCAGGACAGGGACTGGGTCACACACCCTCACACCTACCCGCTCATCAAACCCGGCG GAACGTTCATCAGGACAGGGACTGGGTCACACGCCCTCACACCTACCCGCTCATCAAACCCGGCG A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47783726..47783800 32194978 MeRIP-seq:(Medium) rs764415768 Functional Loss SNV dbSNP153 33..33 33 - - - 86874 RMVar_ID_86874 Human_SNP_ID_362076777 m1A Human chr8 + 47788954 47788954 47788954 CTAAAGGCCCCCAGGCCTGGAGCCTTTGGGTCACCCAAGGCTGCATACATTCTTTCATACATTTT CTAAAGGCCCCCAGGCCTGGAGCCTTTGGGTCTCCCAAGGCTGCATACATTCTTTCATACATTTT A T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47788901..47789025 32194978 MeRIP-seq:(Medium) rs777767203 Functional Loss SNV dbSNP153 33..33 33 - - - 86875 RMVar_ID_86875 Human_SNP_ID_362080084 m1A Human chr8 - 47800927 47800927 47800927 GCAAAAATATTCTGGCTTTCCGTGACCAGAACATTCTCTTGGGTACAACTTACAGGATCATAGCG GCAAAAATATTCTGGCTTTCCGTGACCAGAACGTTCTCTTGGGTACAACTTACAGGATCATAGCG T C PRKDC Ensembl:ENSG00000253729 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47800876..47801000 32194978 MeRIP-seq:(Medium) rs752730508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89427,Human_RBP_ID_1056025,Human_RBP_ID_2055626,Human_RBP_ID_3879120,Human_RBP_ID_8687782,Human_RBP_ID_8920386,Human_RBP_ID_9338644,Human_RBP_ID_9405408,Human_RBP_ID_18391041,Human_RBP_ID_18897166,Human_RBP_ID_26359055 Human_Splice_Rec_975302,Human_Splice_Rec_975472 Human_miRNA_ID_2477487,Human_miRNA_ID_2566734 RMVar_hsa_circ_119878,RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_127310,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251808,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_7017,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_91632,RMVar_hsa_circ_251820,RMVar_hsa_circ_41710,RMVar_hsa_circ_87587,RMVar_hsa_circ_251821,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_76511,RMVar_hsa_circ_98268,RMVar_hsa_circ_85918,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_121529,RMVar_hsa_circ_251827,RMVar_hsa_circ_106499,RMVar_hsa_circ_251828,RMVar_hsa_circ_251829,RMVar_hsa_circ_251830,RMVar_hsa_circ_106825,RMVar_hsa_circ_104608,RMVar_hsa_circ_370867,RMVar_hsa_circ_251831,RMVar_hsa_circ_17562,RMVar_hsa_circ_251835,RMVar_hsa_circ_251836,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_310709,RMVar_hsa_circ_251837,RMVar_hsa_circ_21304,RMVar_hsa_circ_11362,RMVar_hsa_circ_34854,RMVar_hsa_circ_21551,RMVar_hsa_circ_348987,RMVar_hsa_circ_251839,RMVar_hsa_circ_251840,RMVar_hsa_circ_369394,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_58658,RMVar_hsa_circ_251841,RMVar_hsa_circ_251842,RMVar_hsa_circ_251843,RMVar_hsa_circ_279066,RMVar_hsa_circ_327943,RMVar_hsa_circ_374541,RMVar_hsa_circ_323281,RMVar_hsa_circ_103918,RMVar_hsa_circ_251844,RMVar_hsa_circ_251846,RMVar_hsa_circ_251848,RMVar_hsa_circ_5041,RMVar_hsa_circ_251847,RMVar_hsa_circ_251845,RMVar_hsa_circ_105650,RMVar_hsa_circ_292778,RMVar_hsa_circ_348321,RMVar_hsa_circ_372560,RMVar_hsa_circ_109579,RMVar_hsa_circ_59761,RMVar_hsa_circ_251849,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851 86876 RMVar_ID_86876 Human_SNP_ID_362081413 m1A Human chr8 - 47806066 47806066 47806066 GGGGGATGTGATTTAGGGTAGGCTTTATGGGCATGGAAGGATTTGGACATGGGATGGCACTGGGT GGGGGATGTGATTTAGGGTAGGCTTTATGGGCGTGGAAGGATTTGGACATGGGATGGCACTGGGT T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:47806064..47806150 26863196 MeRIP-seq:(Medium) rs896006313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119878,RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_127310,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251808,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_7017,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_91632,RMVar_hsa_circ_251820,RMVar_hsa_circ_41710,RMVar_hsa_circ_87587,RMVar_hsa_circ_251821,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_98268,RMVar_hsa_circ_251825,RMVar_hsa_circ_121529,RMVar_hsa_circ_106499,RMVar_hsa_circ_251828,RMVar_hsa_circ_251829,RMVar_hsa_circ_251830,RMVar_hsa_circ_106825,RMVar_hsa_circ_104608,RMVar_hsa_circ_370867,RMVar_hsa_circ_251831,RMVar_hsa_circ_17562,RMVar_hsa_circ_251835,RMVar_hsa_circ_251836,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_310709,RMVar_hsa_circ_251837,RMVar_hsa_circ_21304,RMVar_hsa_circ_11362,RMVar_hsa_circ_34854,RMVar_hsa_circ_21551,RMVar_hsa_circ_348987,RMVar_hsa_circ_251839,RMVar_hsa_circ_251840,RMVar_hsa_circ_369394,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_58658,RMVar_hsa_circ_251841,RMVar_hsa_circ_251842,RMVar_hsa_circ_251843,RMVar_hsa_circ_279066,RMVar_hsa_circ_327943,RMVar_hsa_circ_374541,RMVar_hsa_circ_323281,RMVar_hsa_circ_103918,RMVar_hsa_circ_251844,RMVar_hsa_circ_251846,RMVar_hsa_circ_251848,RMVar_hsa_circ_5041,RMVar_hsa_circ_251847,RMVar_hsa_circ_251845,RMVar_hsa_circ_105650,RMVar_hsa_circ_292778,RMVar_hsa_circ_372560,RMVar_hsa_circ_109579,RMVar_hsa_circ_59761,RMVar_hsa_circ_251853,RMVar_hsa_circ_124485,RMVar_hsa_circ_343403,RMVar_hsa_circ_251849,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851,RMVar_hsa_circ_357668,RMVar_hsa_circ_343665,RMVar_hsa_circ_272690,RMVar_hsa_circ_329165,RMVar_hsa_circ_127366,RMVar_hsa_circ_251855,RMVar_hsa_circ_251857,RMVar_hsa_circ_116027,RMVar_hsa_circ_251858,RMVar_hsa_circ_251856,RMVar_hsa_circ_251854,RMVar_hsa_circ_251852 86877 RMVar_ID_86877 Human_SNP_ID_362086842 m1A Human chr8 + 47826776 47826776 47826776 GGAGCAGAGCCTCCTCTAGCAGGCGGATGCCCACGGGCTGCTGTAGGCTGGCCAGGCAACCAGCG GGAGCAGAGCCTCCTCTAGCAGGCGGATGCCCGCGGGCTGCTGTAGGCTGGCCAGGCAACCAGCG A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:47826726..47826775 32194978 MeRIP-seq:(Medium) rs776949963 Functional Loss SNV dbSNP153 33..33 33 - - - 86878 RMVar_ID_86878 Human_SNP_ID_362087222 m1A Human chr8 - 47828251 47828251 47828251 ATAAATTTAAGACACTGTCTGAAAAAAACAACATCACTCAAAAGTTGCTTCAAGACTTCAATCGT ATAAATTTAAGACACTGTCTGAAAAAAACAACGTCACTCAAAAGTTGCTTCAAGACTTCAATCGT T C PRKDC Ensembl:ENSG00000253729 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47828201..47828250 32194978 MeRIP-seq:(Medium) rs948862967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2055650,Human_RBP_ID_4987522,Human_RBP_ID_8687806,Human_RBP_ID_17545887,Human_RBP_ID_18119506,Human_RBP_ID_23086312 Human_Splice_Rec_975284,Human_Splice_Rec_975285,Human_Splice_Rec_975454,Human_Splice_Rec_975455 RMVar_hsa_circ_119878,RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251808,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_251825,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_106825,RMVar_hsa_circ_104608,RMVar_hsa_circ_370867,RMVar_hsa_circ_251831,RMVar_hsa_circ_251835,RMVar_hsa_circ_251836,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_251837,RMVar_hsa_circ_11362,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_251843,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_109579,RMVar_hsa_circ_251853,RMVar_hsa_circ_124485,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851,RMVar_hsa_circ_127366,RMVar_hsa_circ_116027,RMVar_hsa_circ_251854,RMVar_hsa_circ_278197,RMVar_hsa_circ_112435,RMVar_hsa_circ_251852,RMVar_hsa_circ_361284,RMVar_hsa_circ_373300,RMVar_hsa_circ_251860,RMVar_hsa_circ_372942,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_71594,RMVar_hsa_circ_251863,RMVar_hsa_circ_31685,RMVar_hsa_circ_251864,RMVar_hsa_circ_251861,RMVar_hsa_circ_251862,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_266412,RMVar_hsa_circ_12669,RMVar_hsa_circ_56439,RMVar_hsa_circ_251867,RMVar_hsa_circ_85515,RMVar_hsa_circ_337032,RMVar_hsa_circ_355728,RMVar_hsa_circ_19420,RMVar_hsa_circ_251868,RMVar_hsa_circ_115271 86879 RMVar_ID_86879 Human_SNP_ID_362087789 m1A Human chr8 - 47830672 47830672 47830672 TGCCCAGGTCGTTCTGTACAGAAGCTACCGGCACGGAGACCTTCCTGACATTCAGATCAAGCACA TGCCCAGGTCGTTCTGTACAGAAGCTACCGGCGCGGAGACCTTCCTGACATTCAGATCAAGCACA T C PRKDC Ensembl:ENSG00000253729 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47830601..47830675 32194978 MeRIP-seq:(Medium) rs773153062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2055651,Human_RBP_ID_7840798,Human_RBP_ID_8920446,Human_RBP_ID_9313431,Human_RBP_ID_16427744,Human_RBP_ID_17545889,Human_RBP_ID_21905436 Human_Splice_Rec_975282,Human_Splice_Rec_975283,Human_Splice_Rec_975452,Human_Splice_Rec_975453 Human_miRNA_ID_2464828,Human_miRNA_ID_2727613 RMVar_hsa_circ_119878,RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251808,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_15990,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_251825,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_104608,RMVar_hsa_circ_370867,RMVar_hsa_circ_251831,RMVar_hsa_circ_251836,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_251837,RMVar_hsa_circ_11362,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_251843,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_109579,RMVar_hsa_circ_251853,RMVar_hsa_circ_124485,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851,RMVar_hsa_circ_127366,RMVar_hsa_circ_116027,RMVar_hsa_circ_251854,RMVar_hsa_circ_278197,RMVar_hsa_circ_112435,RMVar_hsa_circ_251852,RMVar_hsa_circ_361284,RMVar_hsa_circ_373300,RMVar_hsa_circ_251860,RMVar_hsa_circ_372942,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_71594,RMVar_hsa_circ_251863,RMVar_hsa_circ_31685,RMVar_hsa_circ_251864,RMVar_hsa_circ_251861,RMVar_hsa_circ_251862,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_266412,RMVar_hsa_circ_12669,RMVar_hsa_circ_56439,RMVar_hsa_circ_251867,RMVar_hsa_circ_85515,RMVar_hsa_circ_337032,RMVar_hsa_circ_355728,RMVar_hsa_circ_19420,RMVar_hsa_circ_34575,RMVar_hsa_circ_251868,RMVar_hsa_circ_115271,RMVar_hsa_circ_73006,RMVar_hsa_circ_367114 86880 RMVar_ID_86880 Human_SNP_ID_362088640 m1A Human chr8 + 47833650 47833650 47833650 CTTCCTAAAGCTGAAGTTCGACATACACCCCCACACCCACAAGACTGTCCTCACAGCACCCTTTG CTTCCTAAAGCTGAAGTTCGACATACACCCCCCCACCCACAAGACTGTCCTCACAGCACCCTTTG A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:47833626..47833880 26863196 MeRIP-seq:(Medium) rs1312233396 Functional Loss SNV dbSNP153 33..33 33 - - - 86881 RMVar_ID_86881 Human_SNP_ID_362088744 m1A Human chr8 + 47834146 47834146 47834146 CAGTCAGAAATGTCCCCAGACCTGAGCTCTGCAGTAATTTAGTGGGGAAGCTATTTTAAGCACAC CAGTCAGAAATGTCCCCAGACCTGAGCTCTGCCGTAATTTAGTGGGGAAGCTATTTTAAGCACAC A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47834142..47834346 26863196 MeRIP-seq:(Medium) rs764923974 Functional Loss SNV dbSNP153 33..33 33 - - - 86882 RMVar_ID_86882 Human_SNP_ID_362088745 m1A Human chr8 + 47834146 47834146 47834146 CAGTCAGAAATGTCCCCAGACCTGAGCTCTGCAGTAATTTAGTGGGGAAGCTATTTTAAGCACAC CAGTCAGAAATGTCCCCAGACCTGAGCTCTGCTGTAATTTAGTGGGGAAGCTATTTTAAGCACAC A T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47834142..47834346 26863196 MeRIP-seq:(Medium) rs764923974 Functional Loss SNV dbSNP153 33..33 33 - - - 86883 RMVar_ID_86883 Human_SNP_ID_362088754 m1A Human chr8 - 47834179 47834179 47834179 GATAACAAAGTGAAAGGTAAGCTGGGTTGCTGAGTGTGCTTAAAATAGCTTCCCCACTAAATTAC GATAACAAAGTGAAAGGTAAGCTGGGTTGCTGGGTGTGCTTAAAATAGCTTCCCCACTAAATTAC T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:47834176..47834225 26863196 MeRIP-seq:(Medium) rs751535581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19140168 RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_15990,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_251825,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_104608,RMVar_hsa_circ_251831,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_251837,RMVar_hsa_circ_11362,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_251843,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_109579,RMVar_hsa_circ_251853,RMVar_hsa_circ_124485,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851,RMVar_hsa_circ_127366,RMVar_hsa_circ_116027,RMVar_hsa_circ_251854,RMVar_hsa_circ_251852,RMVar_hsa_circ_361284,RMVar_hsa_circ_373300,RMVar_hsa_circ_372942,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_71594,RMVar_hsa_circ_251863,RMVar_hsa_circ_31685,RMVar_hsa_circ_251861,RMVar_hsa_circ_251862,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_266412,RMVar_hsa_circ_12669,RMVar_hsa_circ_56439,RMVar_hsa_circ_251867,RMVar_hsa_circ_85515,RMVar_hsa_circ_337032,RMVar_hsa_circ_355728,RMVar_hsa_circ_19420,RMVar_hsa_circ_84957,RMVar_hsa_circ_34575,RMVar_hsa_circ_251868,RMVar_hsa_circ_115271,RMVar_hsa_circ_73006,RMVar_hsa_circ_367114,RMVar_hsa_circ_109931,RMVar_hsa_circ_251869,RMVar_hsa_circ_251870 86884 RMVar_ID_86884 Human_SNP_ID_362095213 m1A Human chr8 + 47859635 47859635 47859635 GTGATCACCCGTCTCCGAAAACGACCAGTGGCAGGTCTAGGGTCTTGGGAGCTGTATGAATAGCT GTGATCACCCGTCTCCGAAAACGACCAGTGGCTGGTCTAGGGTCTTGGGAGCTGTATGAATAGCT A T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47859601..47859675 32194978 MeRIP-seq:(Medium) rs769146563 Functional Loss SNV dbSNP153 33..33 33 - - - 86885 RMVar_ID_86885 Human_SNP_ID_362102592 m1A Human chr8 + 47888503 47888503 47888503 ATCATACTAAAGCTAAAATAAATGTAAAAACAATAAGTTATAGTTACCTGAGACGGTAATATATT ATCATACTAAAGCTAAAATAAATGTAAAAACAGTAAGTTATAGTTACCTGAGACGGTAATATATT A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47888501..47888675 32194978 MeRIP-seq:(Medium) rs768782547 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 86886 RMVar_ID_86886 Human_SNP_ID_362102791 m1A Human chr8 + 47889069 47889069 47889069 CAGATGGGTCTCTAGGATATCTTTGTATGGGGACATCTTTAGAGCTTTCATCAGATTCACACAAA CAGATGGGTCTCTAGGATATCTTTGTATGGGGGCATCTTTAGAGCTTTCATCAGATTCACACAAA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47889001..47889100 32194978 MeRIP-seq:(Medium) rs1411156285 Functional Loss SNV dbSNP153 33..33 33 - - - 86887 RMVar_ID_86887 Human_SNP_ID_362103167 m1A Human chr8 + 47890394 47890394 47890394 TGTTCTGTTACCTGCTGCCCCAGTGCCAAAGCACTTTTCTGCTGCTATAATGTCATGCATGGCAA TGTTCTGTTACCTGCTGCCCCAGTGCCAAAGCGCTTTTCTGCTGCTATAATGTCATGCATGGCAA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47890251..47890400 32194978 MeRIP-seq:(Medium) rs760839353 Functional Loss SNV dbSNP153 33..33 33 - - - 86888 RMVar_ID_86888 Human_SNP_ID_362118234 m1A Human chr8 - 47946601 47946601 47946601 GTGTGAGCAAGATGAGGAGGGGGTGAGAGTGCAGAGACCAGGCGGAGGGTCTCAAGAGAGTGCTG GTGTGAGCAAGATGAGGAGGGGGTGAGAGTGCCGAGACCAGGCGGAGGGTCTCAAGAGAGTGCTG T G PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:47946360..47946696 26863196 MeRIP-seq:(Medium) rs904143392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845593,Human_RBP_ID_24260393 RMVar_hsa_circ_5464,RMVar_hsa_circ_75887,RMVar_hsa_circ_24652,RMVar_hsa_circ_61234,RMVar_hsa_circ_88681,RMVar_hsa_circ_92750,RMVar_hsa_circ_251902,RMVar_hsa_circ_251903,RMVar_hsa_circ_251901,RMVar_hsa_circ_97106,RMVar_hsa_circ_113996,RMVar_hsa_circ_251916,RMVar_hsa_circ_251917,RMVar_hsa_circ_98984,RMVar_hsa_circ_110167,RMVar_hsa_circ_251928,RMVar_hsa_circ_251929,RMVar_hsa_circ_267210,RMVar_hsa_circ_27732,RMVar_hsa_circ_369481,RMVar_hsa_circ_88331,RMVar_hsa_circ_251937,RMVar_hsa_circ_251938,RMVar_hsa_circ_110232,RMVar_hsa_circ_251949,RMVar_hsa_circ_58991,RMVar_hsa_circ_91368,RMVar_hsa_circ_251959,RMVar_hsa_circ_32533,RMVar_hsa_circ_30209,RMVar_hsa_circ_79236,RMVar_hsa_circ_251961,RMVar_hsa_circ_273855,RMVar_hsa_circ_82443,RMVar_hsa_circ_38403,RMVar_hsa_circ_112334,RMVar_hsa_circ_251966,RMVar_hsa_circ_251967,RMVar_hsa_circ_374965,RMVar_hsa_circ_251968,RMVar_hsa_circ_251969,RMVar_hsa_circ_374161,RMVar_hsa_circ_251972,RMVar_hsa_circ_113617,RMVar_hsa_circ_251976,RMVar_hsa_circ_350569,RMVar_hsa_circ_348819 86889 RMVar_ID_86889 Human_SNP_ID_362122267 m1A Human chr8 - 47960080 47960080 47960080 AGCCGGTGTGCGTTGCTCCCTGCTGCGGCTGCAGGAGACCTTGTCCGCTGCGGACCGCTGCGGTG AGCCGGTGTGCGTTGCTCCCTGCTGCGGCTGCGGGAGACCTTGTCCGCTGCGGACCGCTGCGGTG T C PRKDC Ensembl:ENSG00000253729 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:47960031..47960114 26863196 MeRIP-seq:(Medium) rs1320427747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255201,Human_RBP_ID_796259,Human_RBP_ID_4987905,Human_RBP_ID_5328853,Human_RBP_ID_5534519,Human_RBP_ID_8920682,Human_RBP_ID_9226268,Human_RBP_ID_9313496,Human_RBP_ID_9338266,Human_RBP_ID_18427101,Human_RBP_ID_22465563,Human_RBP_ID_26772342,Human_RBP_ID_27125478 Human_miRNA_ID_2942077 RMVar_hsa_circ_97106,RMVar_hsa_circ_251917,RMVar_hsa_circ_98984,RMVar_hsa_circ_251929,RMVar_hsa_circ_91368,RMVar_hsa_circ_251959,RMVar_hsa_circ_98802,RMVar_hsa_circ_251982 86890 RMVar_ID_86890 Human_SNP_ID_362122279 m1A Human chr8 + 47960096 47960096 47960096 AGCGGACAAGGTCTCCTGCAGCCGCAGCAGGGAGCAACGCACACCGGCTCCGGAGCCCGCCATGC AGCGGACAAGGTCTCCTGCAGCCGCAGCAGGGGGCAACGCACACCGGCTCCGGAGCCCGCCATGC A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:47959951..47960175 26863196 MeRIP-seq:(Medium) rs1476039385 Functional Loss SNV dbSNP153 33..33 33 - - - 86891 RMVar_ID_86891 Human_SNP_ID_362122294 m1A Human chr8 + 47960117 47960117 47960117 CCGCAGCAGGGAGCAACGCACACCGGCTCCGGAGCCCGCCATGCCGCCGAGTCCCGCTCCCGCGC CCGCAGCAGGGAGCAACGCACACCGGCTCCGGTGCCCGCCATGCCGCCGAGTCCCGCTCCCGCGC A T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47960034..47960124 26863196 MeRIP-seq:(Medium) rs1037483837 Functional Loss SNV dbSNP153 33..33 33 - - - 86892 RMVar_ID_86892 Human_SNP_ID_362122705 m1A Human chr8 + 47960996 47960996 47960996 AGGTGGACTCGGAGTCCGCGAGCGTCGTCGGCAAGCGGCCGCCTTTCCACGGTAACCGCGCGCCG AGGTGGACTCGGAGTCCGCGAGCGTCGTCGGCGAGCGGCCGCCTTTCCACGGTAACCGCGCGCCG A G MCM4 Ensembl:ENSG00000104738 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:47960951..47961062;chr8:47960951..47961155 26863196 MeRIP-seq:(Medium) rs1166597379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1336097,Human_RBP_ID_4987914,Human_RBP_ID_8923097,Human_RBP_ID_9313498,Human_RBP_ID_9338267,Human_RBP_ID_17714941,Human_RBP_ID_18119574,Human_RBP_ID_18426693,Human_RBP_ID_19022903,Human_RBP_ID_22465564,Human_RBP_ID_23088091 Human_Splice_Rec_975553,Human_Splice_Rec_975581,Human_Splice_Rec_975613,Human_Splice_Rec_975673,Human_Splice_Rec_975705,Human_Splice_Rec_975707,Human_Splice_Rec_975739 RMVar_hsa_circ_78876,RMVar_hsa_circ_107165,RMVar_hsa_circ_93440,RMVar_hsa_circ_251983,RMVar_hsa_circ_251984,RMVar_hsa_circ_251985 86893 RMVar_ID_86893 Human_SNP_ID_362122789 m1A Human chr8 + 47961163 47961163 47961163 GTACTCCGAGCACTATGTCGTCCCCGGCGTCGACCCCGAGCCGCCGCGGCAGCCGGCGTGGAAGG GTACTCCGAGCACTATGTCGTCCCCGGCGTCGCCCCCGAGCCGCCGCGGCAGCCGGCGTGGAAGG A C MCM4 Ensembl:ENSG00000104738 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:47960926..47961250 26863410 MeRIP-seq:(Medium) rs940419261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254809,Human_RBP_ID_4995490,Human_RBP_ID_5329114,Human_RBP_ID_8923098,Human_RBP_ID_9313501,Human_RBP_ID_9338268,Human_RBP_ID_19022904,Human_RBP_ID_22534376,Human_RBP_ID_23088092,Human_RBP_ID_26358727 Human_Splice_Rec_975546,Human_Splice_Rec_975547,Human_Splice_Rec_975554,Human_Splice_Rec_975555,Human_Splice_Rec_975582,Human_Splice_Rec_975583,Human_Splice_Rec_975643,Human_Splice_Rec_975674,Human_Splice_Rec_975675,Human_Splice_Rec_975706,Human_Splice_Rec_975708,Human_Splice_Rec_975740,Human_Splice_Rec_975741,Human_Splice_Rec_975747 RMVar_hsa_circ_78876,RMVar_hsa_circ_107165,RMVar_hsa_circ_93440,RMVar_hsa_circ_251983,RMVar_hsa_circ_251984,RMVar_hsa_circ_251985 86894 RMVar_ID_86894 Human_SNP_ID_362122790 m1A Human chr8 + 47961163 47961163 47961163 GTACTCCGAGCACTATGTCGTCCCCGGCGTCGACCCCGAGCCGCCGCGGCAGCCGGCGTGGAAGG GTACTCCGAGCACTATGTCGTCCCCGGCGTCGGCCCCGAGCCGCCGCGGCAGCCGGCGTGGAAGG A G MCM4 Ensembl:ENSG00000104738 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:47960926..47961250 26863410 MeRIP-seq:(Medium) rs940419261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254809,Human_RBP_ID_4995490,Human_RBP_ID_5329114,Human_RBP_ID_8923098,Human_RBP_ID_9313501,Human_RBP_ID_9338268,Human_RBP_ID_19022904,Human_RBP_ID_22534376,Human_RBP_ID_23088092,Human_RBP_ID_26358727 Human_Splice_Rec_975546,Human_Splice_Rec_975547,Human_Splice_Rec_975554,Human_Splice_Rec_975555,Human_Splice_Rec_975582,Human_Splice_Rec_975583,Human_Splice_Rec_975643,Human_Splice_Rec_975674,Human_Splice_Rec_975675,Human_Splice_Rec_975706,Human_Splice_Rec_975708,Human_Splice_Rec_975740,Human_Splice_Rec_975741,Human_Splice_Rec_975747 RMVar_hsa_circ_78876,RMVar_hsa_circ_107165,RMVar_hsa_circ_93440,RMVar_hsa_circ_251983,RMVar_hsa_circ_251984,RMVar_hsa_circ_251985 86895 RMVar_ID_86895 Human_SNP_ID_362126604 m1A Human chr8 + 47972952 47972952 47972952 CCACCTGGTCGCACTGTACTACCAGAGCGAGGAGCAGGCAGAGGAGGAGCTCCTGGACATGGCGG CCACCTGGTCGCACTGTACTACCAGAGCGAGGGGCAGGCAGAGGAGGAGCTCCTGGACATGGCGG A G MCM4 Ensembl:ENSG00000104738 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47972901..47973028 26863196 MeRIP-seq:(Medium) rs1255002943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254818,Human_RBP_ID_795533,Human_RBP_ID_2055888,Human_RBP_ID_7841523,Human_RBP_ID_8923117,Human_RBP_ID_9405460,Human_RBP_ID_16431629,Human_RBP_ID_22464941,Human_RBP_ID_23088094,Human_RBP_ID_26359072 Human_Splice_Rec_975578,Human_Splice_Rec_975606,Human_Splice_Rec_975636,Human_Splice_Rec_975666,Human_Splice_Rec_975698,Human_Splice_Rec_975732,Human_Splice_Rec_975766,Human_Splice_Rec_975800,Human_Splice_Rec_975818,Human_Splice_Rec_975826,Human_Splice_Rec_975842 Human_miRNA_ID_2357211,Human_miRNA_ID_3059652 RMVar_hsa_circ_107165,RMVar_hsa_circ_93440,RMVar_hsa_circ_251983,RMVar_hsa_circ_251984,RMVar_hsa_circ_40998,RMVar_hsa_circ_82868,RMVar_hsa_circ_251989,RMVar_hsa_circ_375596,RMVar_hsa_circ_35133,RMVar_hsa_circ_251993,RMVar_hsa_circ_335625,RMVar_hsa_circ_251992,RMVar_hsa_circ_251997,RMVar_hsa_circ_252000,RMVar_hsa_circ_375047,RMVar_hsa_circ_377519,RMVar_hsa_circ_290618,RMVar_hsa_circ_252001,RMVar_hsa_circ_251999,RMVar_hsa_circ_252004,RMVar_hsa_circ_329281,RMVar_hsa_circ_322599,RMVar_hsa_circ_252003 86896 RMVar_ID_86896 Human_SNP_ID_362127840 m1A Human chr8 + 47976788 47976788 47976788 GGAAGACCGTGCGCTTGCTCTGAAGCCTTGTGAGCAAGGAAGGCTCCCTGCATGTCCTGCTTGCT GGAAGACCGTGCGCTTGCTCTGAAGCCTTGTGGGCAAGGAAGGCTCCCTGCATGTCCTGCTTGCT A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47976739..47976856 26863196 MeRIP-seq:(Medium) rs1563837238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700763,Human_RBP_ID_1697755,Human_RBP_ID_2055910,Human_RBP_ID_5001839,Human_RBP_ID_8688057,Human_RBP_ID_9313520,Human_RBP_ID_16431753,Human_RBP_ID_17666112,Human_RBP_ID_18119600,Human_RBP_ID_18897478,Human_RBP_ID_21905443,Human_RBP_ID_22464943,Human_RBP_ID_22517174,Human_RBP_ID_22776065,Human_RBP_ID_27125546 Human_miRNA_ID_2779558 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983,RMVar_hsa_circ_251992,RMVar_hsa_circ_251997,RMVar_hsa_circ_377519,RMVar_hsa_circ_252001 86897 RMVar_ID_86897 Human_SNP_ID_362127860 m1A Human chr8 - 47976853 47976853 47976853 GACTTTAAGCTCTATTTACACTGATGGCGGCCAACTGAGATGCAGACCACACCCATGTGGCGTGC GACTTTAAGCTCTATTTACACTGATGGCGGCCGACTGAGATGCAGACCACACCCATGTGGCGTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47975701..47977000 32194978 MeRIP-seq:(Medium) rs1167626176 Functional Loss SNV dbSNP153 33..33 33 - - - 86898 RMVar_ID_86898 Human_SNP_ID_362128060 m1A Human chr8 + 47977576 47977576 47977576 TGGCTAGAGTACACTGGTACAATCACGGCTCAATGTAGGCTTAACCTCCTGGGCTCAGGTGTATG TGGCTAGAGTACACTGGTACAATCACGGCTCACTGTAGGCTTAACCTCCTGGGCTCAGGTGTATG A C MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47977526..47978011 32194978 MeRIP-seq:(Medium) rs756962896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700785,Human_RBP_ID_7841588,Human_RBP_ID_8688061,Human_RBP_ID_9226282,Human_RBP_ID_16431786,Human_RBP_ID_17318255,Human_RBP_ID_17545927,Human_RBP_ID_18391109,Human_RBP_ID_24260516 Human_Splice_Rec_975851 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 86899 RMVar_ID_86899 Human_SNP_ID_362128061 m1A Human chr8 + 47977576 47977576 47977576 TGGCTAGAGTACACTGGTACAATCACGGCTCAATGTAGGCTTAACCTCCTGGGCTCAGGTGTATG TGGCTAGAGTACACTGGTACAATCACGGCTCAGTGTAGGCTTAACCTCCTGGGCTCAGGTGTATG A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:47977526..47978011 32194978 MeRIP-seq:(Medium) rs756962896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700785,Human_RBP_ID_7841588,Human_RBP_ID_8688061,Human_RBP_ID_9226282,Human_RBP_ID_16431786,Human_RBP_ID_17318255,Human_RBP_ID_17545927,Human_RBP_ID_18391109,Human_RBP_ID_24260516 Human_Splice_Rec_975851 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 86900 RMVar_ID_86900 Human_SNP_ID_362133246 m1A Human chr8 + 47998008 47998008 47998008 GAGGATAATTTGAAAAGTAGAGCAAGACTGGCAGAGGGAAGGATGACTACAGAGAGTAAAGAAAG GAGGATAATTTGAAAAGTAGAGCAAGACTGGCGGAGGGAAGGATGACTACAGAGAGTAAAGAAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:47997842..47998044 26863196 MeRIP-seq:(Medium) rs1438747337 Functional Loss SNV dbSNP153 33..33 33 - - - 86901 RMVar_ID_86901 Human_SNP_ID_362136064 m1A Human chr8 + 48008467 48008467 48008467 GCGTCGGGCTGCAGGAGAAGATGGCGGTCTCCACAGGTCGGTTCCCGGGCCGGGCTGCGTGATTT GCGTCGGGCTGCAGGAGAAGATGGCGGTCTCCGCAGGTCGGTTCCCGGGCCGGGCTGCGTGATTT A G UBE2V2 Ensembl:ENSG00000169139 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:48008452..48008572 26863196 MeRIP-seq:(Medium) rs749329628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795972,Human_RBP_ID_845331,Human_RBP_ID_5223650 Human_Splice_Rec_975853,Human_Splice_Rec_975857,Human_Splice_Rec_975865,Human_Splice_Rec_975871 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 86902 RMVar_ID_86902 Human_SNP_ID_362136065 m1A Human chr8 - 48008472 48008472 48008472 GCGGAAAATCACGCAGCCCGGCCCGGGAACCGACCTGTGGAGACCGCCATCTTCTCCTGCAGCCC GCGGAAAATCACGCAGCCCGGCCCGGGAACCGCCCTGTGGAGACCGCCATCTTCTCCTGCAGCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:48008426..48008529 26863196 MeRIP-seq:(Medium) rs771019920 Functional Loss SNV dbSNP153 33..33 33 - - - 86903 RMVar_ID_86903 Human_SNP_ID_362136162 m1A Human chr8 - 48008678 48008678 48008678 CACCCCGCCCCCAGCCCGCCGGCGCGCGGCCGACGCGCGAGCACGACCCGCCAACCCGACGGCCG CACCCCGCCCCCAGCCCGCCGGCGCGCGGCCGTCGCGCGAGCACGACCCGCCAACCCGACGGCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:48008675..48008755 26863196 MeRIP-seq:(Medium) rs1449206248 Functional Loss SNV dbSNP153 33..33 33 - - - 86904 RMVar_ID_86904 Human_SNP_ID_362145247 m1A Human chr8 + 48043029 48043029 48043029 AGCTTTTTACATTTACACTGACGTTCTTTTGTATAGGAGTTAAAGTTCCTCGTAATTTTCGCTTG AGCTTTTTACATTTACACTGACGTTCTTTTGTGTAGGAGTTAAAGTTCCTCGTAATTTTCGCTTG A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:48043026..48043150 26863196 MeRIP-seq:(Medium) rs755986461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 86905 RMVar_ID_86905 Human_SNP_ID_362145275 m1A Human chr8 + 48043126 48043126 48043126 AGGCGACGGTACAGTTAGCTGGGGCCTTGAAGATGATGAAGATATGACACTTACAAGGTGGACAG AGGCGACGGTACAGTTAGCTGGGGCCTTGAAGGTGATGAAGATATGACACTTACAAGGTGGACAG A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:48043076..48043175 32194978 MeRIP-seq:(Medium) rs1243447037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89012,Human_RBP_ID_700814,Human_RBP_ID_960584,Human_RBP_ID_1697799,Human_RBP_ID_2055942,Human_RBP_ID_7841792,Human_RBP_ID_9405463,Human_RBP_ID_16432717,Human_RBP_ID_18124947,Human_RBP_ID_23140894,Human_RBP_ID_26359077,Human_RBP_ID_27831880 Human_Splice_Rec_975860,Human_Splice_Rec_975861,Human_Splice_Rec_975866,Human_Splice_Rec_975867,Human_Splice_Rec_975872,Human_Splice_Rec_975873,Human_Splice_Rec_975880,Human_Splice_Rec_975881,Human_Splice_Rec_975885,Human_Splice_Rec_975889 RMVar_hsa_circ_82333,RMVar_hsa_circ_252007,RMVar_hsa_circ_278115,RMVar_hsa_circ_252006,RMVar_hsa_circ_296655,RMVar_hsa_circ_252008 86906 RMVar_ID_86906 Human_SNP_ID_362364899 m1A Human chr8 + 48921301 48921301 48921301 GCCAGCGGGTCTGGCGGGCGCCCGGCGCGGATAACGGTCCGGCGGGAGGACACGGCGGTCCCTAC GCCAGCGGGTCTGGCGGGCGCCCGGCGCGGATGACGGTCCGGCGGGAGGACACGGCGGTCCCTAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:48921251..48921425 26863196 MeRIP-seq:(Medium) rs751125107 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_469 86907 RMVar_ID_86907 Human_SNP_ID_362364900 m1A Human chr8 + 48921301 48921301 48921301 GCCAGCGGGTCTGGCGGGCGCCCGGCGCGGATAACGGTCCGGCGGGAGGACACGGCGGTCCCTAC GCCAGCGGGTCTGGCGGGCGCCCGGCGCGGATTACGGTCCGGCGGGAGGACACGGCGGTCCCTAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:48921251..48921425 26863196 MeRIP-seq:(Medium) rs751125107 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_469 86908 RMVar_ID_86908 Human_SNP_ID_362364915 m1A Human chr8 - 48921327 48921327 48921327 GCCCGAGCCTGGCCCGCCGCGATGCTGTAGGGACCGCCGTGTCCTCCCGCCGGACCGTTATCCGC GCCCGAGCCTGGCCCGCCGCGATGCTGTAGGGGCCGCCGTGTCCTCCCGCCGGACCGTTATCCGC T C SNAI2 Ensembl:ENSG00000019549 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr8:48921279..48921378;chr8:48920436..48921427 26863196,26863410 MeRIP-seq:(Medium) rs1438936163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_180344 86909 RMVar_ID_86909 Human_SNP_ID_363148449 m1A Human chr8 - 51817881 51817881 51817881 CCTAGAACCGTGGCATGTTTTGCCTGAAACATACAGTGAGTTAGAGACAGGGCCTAAGATAGCTT CCTAGAACCGTGGCATGTTTTGCCTGAAACATGCAGTGAGTTAGAGACAGGGCCTAAGATAGCTT T C PCMTD1 Ensembl:ENSG00000168300 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24260791 GWAS_ID_10642,GWAS_ID_10643,GWAS_ID_10644 RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 86910 RMVar_ID_86910 Human_SNP_ID_363149062 m1A Human chr8 - 51819485 51819485 51819485 AAAAGCAAAACCATTGTTATGTGTGACTCTTGATAGGACACAGAACGAGTGAATGAGCATGAGTG AAAAGCAAAACCATTGTTATGTGTGACTCTTGGTAGGACACAGAACGAGTGAATGAGCATGAGTG T C PCMTD1 Ensembl:ENSG00000168300 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs34424720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3161669,Human_RBP_ID_3879444,Human_RBP_ID_7842351,Human_RBP_ID_16433498,Human_RBP_ID_17171809,Human_RBP_ID_24260810 Human_miRNA_ID_968012,Human_miRNA_ID_3013044 GWAS_ID_10645,GWAS_ID_10646,GWAS_ID_10647,GWAS_ID_10648,GWAS_ID_10649,GWAS_ID_10650,GWAS_ID_10651,GWAS_ID_10652,GWAS_ID_10653,GWAS_ID_10654,GWAS_ID_10655,GWAS_ID_10656,GWAS_ID_10657,GWAS_ID_10658,GWAS_ID_10659,GWAS_ID_10660,GWAS_ID_10661,GWAS_ID_10662,GWAS_ID_10663,GWAS_ID_10664,GWAS_ID_10665,GWAS_ID_10666,GWAS_ID_10667,GWAS_ID_10668,GWAS_ID_10669,GWAS_ID_10670,GWAS_ID_10671,GWAS_ID_10672,GWAS_ID_10673 RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 86911 RMVar_ID_86911 Human_SNP_ID_363149063 m1A Human chr8 - 51819485 51819485 51819485 AAAAGCAAAACCATTGTTATGTGTGACTCTTGATAGGACACAGAACGAGTGAATGAGCATGAGTG AAAAGCAAAACCATTGTTATGTGTGACTCTTGCTAGGACACAGAACGAGTGAATGAGCATGAGTG T G PCMTD1 Ensembl:ENSG00000168300 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs34424720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3161669,Human_RBP_ID_3879444,Human_RBP_ID_7842351,Human_RBP_ID_16433498,Human_RBP_ID_17171809,Human_RBP_ID_24260810 Human_miRNA_ID_968012,Human_miRNA_ID_3013044 GWAS_ID_10645,GWAS_ID_10646,GWAS_ID_10647,GWAS_ID_10648,GWAS_ID_10649,GWAS_ID_10650,GWAS_ID_10651,GWAS_ID_10652,GWAS_ID_10653,GWAS_ID_10654,GWAS_ID_10655,GWAS_ID_10656,GWAS_ID_10657,GWAS_ID_10658,GWAS_ID_10659,GWAS_ID_10660,GWAS_ID_10661,GWAS_ID_10662,GWAS_ID_10663,GWAS_ID_10664,GWAS_ID_10665,GWAS_ID_10666,GWAS_ID_10667,GWAS_ID_10668,GWAS_ID_10669,GWAS_ID_10670,GWAS_ID_10671,GWAS_ID_10672,GWAS_ID_10673 RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 86912 RMVar_ID_86912 Human_SNP_ID_363167972 m1A Human chr8 + 51892404 51892404 51892404 TACCCATCACCACTACCATCCCAACTCTTCCAACTCGATTGTCAACTATGGCTTCTAGCAAATGT TACCCATCACCACTACCATCCCAACTCTTCCAGCTCGATTGTCAACTATGGCTTCTAGCAAATGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:51892354..51892437 26863196 MeRIP-seq:(Medium) rs557932568 Functional Loss SNV dbSNP153 33..33 33 - - - 86913 RMVar_ID_86913 Human_SNP_ID_363169768 m1A Human chr8 + 51898742 51898742 51898742 AAGTCCTCCGCCCCCGGCCCGTCCTTCCCCCAACCTGCCCCGCAGCGCCTCAGTTTCCTGGCCCC AAGTCCTCCGCCCCCGGCCCGTCCTTCCCCCACCCTGCCCCGCAGCGCCTCAGTTTCCTGGCCCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:51898701..51899000 26863196 MeRIP-seq:(Medium) rs1447068329 Functional Loss SNV dbSNP153 33..33 33 - - - 86914 RMVar_ID_86914 Human_SNP_ID_363169769 m1A Human chr8 + 51898742 51898742 51898742 AAGTCCTCCGCCCCCGGCCCGTCCTTCCCCCAACCTGCCCCGCAGCGCCTCAGTTTCCTGGCCCC AAGTCCTCCGCCCCCGGCCCGTCCTTCCCCCAGCCTGCCCCGCAGCGCCTCAGTTTCCTGGCCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:51898701..51899000 26863196 MeRIP-seq:(Medium) rs1447068329 Functional Loss SNV dbSNP153 33..33 33 - - - 86915 RMVar_ID_86915 Human_SNP_ID_363169785 m1A Human chr8 - 51898789 51898789 51898789 GGCAGCCGAAGAGTCGGGGGCAGGGGGACTTAAGGGCGGGCAGGTCGGGGGCCAGGAAACTGAGG GGCAGCCGAAGAGTCGGGGGCAGGGGGACTTATGGGCGGGCAGGTCGGGGGCCAGGAAACTGAGG T A PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:51898594..51899057 26863196 MeRIP-seq:(Medium) rs1385834030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7842701,Human_RBP_ID_8221079,Human_RBP_ID_18960901,Human_RBP_ID_26795182 RMVar_hsa_circ_124656,RMVar_hsa_circ_252046 86916 RMVar_ID_86916 Human_SNP_ID_363169792 m1A Human chr8 + 51898808 51898808 51898808 GACCTGCCCGCCCTTAAGTCCCCCTGCCCCCGACTCTTCGGCTGCCGTCCCCCTGGCCCTCTGGC GACCTGCCCGCCCTTAAGTCCCCCTGCCCCCGTCTCTTCGGCTGCCGTCCCCCTGGCCCTCTGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:51898662..51899065 26863196 MeRIP-seq:(Medium) rs1344324266 Functional Loss SNV dbSNP153 33..33 33 - - - 86917 RMVar_ID_86917 Human_SNP_ID_363336589 m1A Human chr8 + 52565315 52565315 52565315 GAGACTCCGGGAGGATCCCGACGCAGGTCCGGAGGGTGCGCGGCCCAAGAGAAGGCCAGCGGGAC GAGACTCCGGGAGGATCCCGACGCAGGTCCGGCGGGTGCGCGGCCCAAGAGAAGGCCAGCGGGAC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:52565214..52565425 26863410 MeRIP-seq:(Medium) rs988163728 Functional Loss SNV dbSNP153 33..33 33 - - - 86918 RMVar_ID_86918 Human_SNP_ID_363336590 m1A Human chr8 + 52565315 52565315 52565315 GAGACTCCGGGAGGATCCCGACGCAGGTCCGGAGGGTGCGCGGCCCAAGAGAAGGCCAGCGGGAC GAGACTCCGGGAGGATCCCGACGCAGGTCCGGGGGGTGCGCGGCCCAAGAGAAGGCCAGCGGGAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:52565214..52565425 26863410 MeRIP-seq:(Medium) rs988163728 Functional Loss SNV dbSNP153 33..33 33 - - - 86919 RMVar_ID_86919 Human_SNP_ID_363375905 m1A Human chr8 + 52714401 52714401 52714401 GAGGCAACGCCGAGGGCTCGGCAGGGCCGCGGACACCGCCGCGGCTTGGTTTGTTATTGTCGACT GAGGCAACGCCGAGGGCTCGGCAGGGCCGCGGCCACCGCCGCGGCTTGGTTTGTTATTGTCGACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr8:52714223..52714433;chr8:52714226..52714425 26863196 MeRIP-seq:(Medium) rs1281571260 Functional Loss SNV dbSNP153 33..33 33 - - - 86920 RMVar_ID_86920 Human_SNP_ID_363655915 m1A Human chr8 + 53795660 53795660 53795660 ACCAACATAAAACACTTACACGAAATGCTGCAAGAATGATTCTTGTTACTTTCTCTTTGACAGAC ACCAACATAAAACACTTACACGAAATGCTGCAGGAATGATTCTTGTTACTTTCTCTTTGACAGAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:53795651..53801874 32194978 MeRIP-seq:(Medium) rs1448198632 Functional Loss SNV dbSNP153 33..33 33 - - - 86921 RMVar_ID_86921 Human_SNP_ID_363659437 m1A Human chr8 - 53811181 53811181 53811181 TGCGTGGTAGCGGTGTTGCTGTTGAAACAGGAACAGTCTCTTCAAGTGATGTAAGTATATTCCTT TGCGTGGTAGCGGTGTTGCTGTTGAAACAGGAGCAGTCTCTTCAAGTGATGTAAGTATATTCCTT T C ATP6V1H Ensembl:ENSG00000047249 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:53811173..53814718 32194978 MeRIP-seq:(Medium) rs761714701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19022030,Human_RBP_ID_24261406 Human_Splice_Rec_977656,Human_Splice_Rec_977657,Human_Splice_Rec_977710,Human_Splice_Rec_977711,Human_Splice_Rec_977740,Human_Splice_Rec_977741,Human_Splice_Rec_977766,Human_Splice_Rec_977767,Human_Splice_Rec_977794,Human_Splice_Rec_977795,Human_Splice_Rec_977802,Human_Splice_Rec_977803 RMVar_hsa_circ_3568,RMVar_hsa_circ_126032,RMVar_hsa_circ_273145,RMVar_hsa_circ_62306,RMVar_hsa_circ_252099,RMVar_hsa_circ_252100,RMVar_hsa_circ_320079,RMVar_hsa_circ_308096,RMVar_hsa_circ_40992,RMVar_hsa_circ_353185,RMVar_hsa_circ_291915,RMVar_hsa_circ_252107,RMVar_hsa_circ_340075,RMVar_hsa_circ_31897,RMVar_hsa_circ_290532,RMVar_hsa_circ_366128,RMVar_hsa_circ_274239,RMVar_hsa_circ_24747,RMVar_hsa_circ_66035,RMVar_hsa_circ_252110,RMVar_hsa_circ_252111,RMVar_hsa_circ_290070,RMVar_hsa_circ_361558,RMVar_hsa_circ_376898,RMVar_hsa_circ_110413,RMVar_hsa_circ_252112,RMVar_hsa_circ_55353,RMVar_hsa_circ_277218,RMVar_hsa_circ_353055,RMVar_hsa_circ_252113 86922 RMVar_ID_86922 Human_SNP_ID_363659438 m1A Human chr8 - 53811181 53811181 53811181 TGCGTGGTAGCGGTGTTGCTGTTGAAACAGGAACAGTCTCTTCAAGTGATGTAAGTATATTCCTT TGCGTGGTAGCGGTGTTGCTGTTGAAACAGGACCAGTCTCTTCAAGTGATGTAAGTATATTCCTT T G ATP6V1H Ensembl:ENSG00000047249 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:53811173..53814718 32194978 MeRIP-seq:(Medium) rs761714701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19022030,Human_RBP_ID_24261406 Human_Splice_Rec_977656,Human_Splice_Rec_977657,Human_Splice_Rec_977710,Human_Splice_Rec_977711,Human_Splice_Rec_977740,Human_Splice_Rec_977741,Human_Splice_Rec_977766,Human_Splice_Rec_977767,Human_Splice_Rec_977794,Human_Splice_Rec_977795,Human_Splice_Rec_977802,Human_Splice_Rec_977803 RMVar_hsa_circ_3568,RMVar_hsa_circ_126032,RMVar_hsa_circ_273145,RMVar_hsa_circ_62306,RMVar_hsa_circ_252099,RMVar_hsa_circ_252100,RMVar_hsa_circ_320079,RMVar_hsa_circ_308096,RMVar_hsa_circ_40992,RMVar_hsa_circ_353185,RMVar_hsa_circ_291915,RMVar_hsa_circ_252107,RMVar_hsa_circ_340075,RMVar_hsa_circ_31897,RMVar_hsa_circ_290532,RMVar_hsa_circ_366128,RMVar_hsa_circ_274239,RMVar_hsa_circ_24747,RMVar_hsa_circ_66035,RMVar_hsa_circ_252110,RMVar_hsa_circ_252111,RMVar_hsa_circ_290070,RMVar_hsa_circ_361558,RMVar_hsa_circ_376898,RMVar_hsa_circ_110413,RMVar_hsa_circ_252112,RMVar_hsa_circ_55353,RMVar_hsa_circ_277218,RMVar_hsa_circ_353055,RMVar_hsa_circ_252113 86923 RMVar_ID_86923 Human_SNP_ID_363667239 m1A Human chr8 - 53843182 53843182 53843182 GGTGCGGGACCCGCTTCACTTTCGGCTCCCGGAGTCTCCCTCCACTGCTCAGACCTCTGGACCTG GGTGCGGGACCCGCTTCACTTTCGGCTCCCGGGGTCTCCCTCCACTGCTCAGACCTCTGGACCTG T C ATP6V1H Ensembl:ENSG00000047249 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:53843134..53843227 26863196 MeRIP-seq:(Medium) rs927806546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255233,Human_RBP_ID_4995498,Human_RBP_ID_5481419,Human_RBP_ID_22115014 86924 RMVar_ID_86924 Human_SNP_ID_363732124 m1A Human chr8 - 54100936 54100936 54100936 TGCTTATTAATTTTCCTCTTCTCTTATAGGTGATTTTCCTGCATGGATTGGGAGATACTGGGTAG TGCTTATTAATTTTCCTCTTCTCTTATAGGTGGTTTTCCTGCATGGATTGGGAGATACTGGGTAG T C LYPLA1 Ensembl:ENSG00000120992 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:54100901..54101418 32194978 MeRIP-seq:(Medium) rs756705739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960118,Human_RBP_ID_4995508,Human_RBP_ID_5405337,Human_RBP_ID_9351571,Human_RBP_ID_19022917,Human_RBP_ID_19140186,Human_RBP_ID_22689187 Human_Splice_Rec_978054,Human_Splice_Rec_978055,Human_Splice_Rec_978070,Human_Splice_Rec_978071,Human_Splice_Rec_978086,Human_Splice_Rec_978087,Human_Splice_Rec_978100,Human_Splice_Rec_978101,Human_Splice_Rec_978114,Human_Splice_Rec_978115,Human_Splice_Rec_978128,Human_Splice_Rec_978129,Human_Splice_Rec_978140,Human_Splice_Rec_978141,Human_Splice_Rec_978154,Human_Splice_Rec_978155,Human_Splice_Rec_978166,Human_Splice_Rec_978167,Human_Splice_Rec_978176,Human_Splice_Rec_978177,Human_Splice_Rec_978188,Human_Splice_Rec_978189,Human_Splice_Rec_978196,Human_Splice_Rec_978197,Human_Splice_Rec_978208 RMVar_hsa_circ_94419,RMVar_hsa_circ_252142 86925 RMVar_ID_86925 Human_SNP_ID_363732533 m1A Human chr8 - 54101964 54101953 54101965 GGGCGGACCCTGGACGCGCGGGCGCGCGCGGAAGGTAGCGCGGGGCCGCGTTGGCGCGCACGCGC GGGCGGACCCTGGACGCGCGGGCGCGCGCGG____________GGCCGCGTTGGCGCGCACGCGC CCCGCGCTACCTT C LYPLA1 Ensembl:ENSG00000120992 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:54101866..54102017 26863410 MeRIP-seq:(Medium) rs1462498229 Functional Loss DEL dbSNP153 32..43 33 - - - RMVar_hsa_circ_94419,RMVar_hsa_circ_252142 86926 RMVar_ID_86926 Human_SNP_ID_363817737 m1A Human chr8 + 54458364 54458364 54458364 AGTCCCGTATCCGGCGGCCGATGAACGCTTTCATGGTGTGGGCTAAGGACGAGCGCAAGCGGCTG AGTCCCGTATCCGGCGGCCGATGAACGCTTTCCTGGTGTGGGCTAAGGACGAGCGCAAGCGGCTG A C SOX17 Ensembl:ENSG00000164736 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:54457930..54458376 26863196 MeRIP-seq:(Medium) rs747896231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_978235 86927 RMVar_ID_86927 Human_SNP_ID_364157989 m1A Human chr8 + 55785768 55785768 55785768 GAAGAGGAAGGTGGTTATTCCTGTGGTACTGCAGAATCACATGACAGCAAAGGCATAGGCCTGGA GAAGAGGAAGGTGGTTATTCCTGTGGTACTGCGGAATCACATGACAGCAAAGGCATAGGCCTGGA A G TGS1 Ensembl:ENSG00000137574 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:55785680..55785831 26863196 MeRIP-seq:(Medium) rs1327249392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2056138,Human_RBP_ID_9226836,Human_RBP_ID_18414275,Human_RBP_ID_26359084 Human_Splice_Rec_978540,Human_Splice_Rec_978560 RMVar_hsa_circ_4472,RMVar_hsa_circ_117047,RMVar_hsa_circ_117781,RMVar_hsa_circ_310354,RMVar_hsa_circ_326332,RMVar_hsa_circ_252160,RMVar_hsa_circ_332160,RMVar_hsa_circ_319355,RMVar_hsa_circ_283098,RMVar_hsa_circ_289451,RMVar_hsa_circ_269930,RMVar_hsa_circ_252163,RMVar_hsa_circ_51905,RMVar_hsa_circ_112537,RMVar_hsa_circ_252165,RMVar_hsa_circ_252167,RMVar_hsa_circ_252168,RMVar_hsa_circ_252166,RMVar_hsa_circ_252164,RMVar_hsa_circ_288557,RMVar_hsa_circ_252161,RMVar_hsa_circ_252162,RMVar_hsa_circ_308557,RMVar_hsa_circ_347086,RMVar_hsa_circ_293017,RMVar_hsa_circ_266157,RMVar_hsa_circ_285064,RMVar_hsa_circ_24599,RMVar_hsa_circ_252170,RMVar_hsa_circ_252171,RMVar_hsa_circ_252172,RMVar_hsa_circ_252169 86928 RMVar_ID_86928 Human_SNP_ID_364173588 m1A Human chr8 + 55842733 55842733 55842733 GAGTGTCCTCTGGCTTCGCCCTCCTCAGGCACAGTTCACCATCTTTGGGGTCCTAACACGTGCAC GAGTGTCCTCTGGCTTCGCCCTCCTCAGGCACCGTTCACCATCTTTGGGGTCCTAACACGTGCAC A C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr8:55842626..55842828;chr8:55842655..55842804 26863196 MeRIP-seq:(Medium) rs1202595791 Functional Loss SNV dbSNP153 33..33 33 - - - 86929 RMVar_ID_86929 Human_SNP_ID_364173599 m1A Human chr8 - 55842767 55842760 55842767 TGTTGGGAAATTGGTATGGGGGAGTGAAGCACAGGTGCACGTGTTAGGACCCCAAAGATGGTGAA TGTTGGGAAATTGGTATGGGGGAGTGAAGCAC_______CGTGTTAGGACCCCAAAGATGGTGAA GTGCACCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:55842719..55842809 26863196 MeRIP-seq:(Medium) rs922744262 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_3179016,Human_RBP_ID_24274944,Human_RBP_ID_24520647 86930 RMVar_ID_86930 Human_SNP_ID_364173605 m1A Human chr8 - 55842767 55842767 55842767 TGTTGGGAAATTGGTATGGGGGAGTGAAGCACAGGTGCACGTGTTAGGACCCCAAAGATGGTGAA TGTTGGGAAATTGGTATGGGGGAGTGAAGCACGGGTGCACGTGTTAGGACCCCAAAGATGGTGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:55842719..55842809 26863196 MeRIP-seq:(Medium) rs1006616299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3179016,Human_RBP_ID_24274944,Human_RBP_ID_24520647 86931 RMVar_ID_86931 Human_SNP_ID_364182655 m1A Human chr8 + 55879927 55879927 55879927 GGCCAGACGCGCTGCAGCCTCCAGCCCGCGGCAAGCGGGGCGGCCGCGCCACCCCCGGCCCCGCG GGCCAGACGCGCTGCAGCCTCCAGCCCGCGGCTAGCGGGGCGGCCGCGCCACCCCCGGCCCCGCG A T LYN Ensembl:ENSG00000254087 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr8:55879826..55880000;chr8:55879826..55880100 26863410 MeRIP-seq:(Medium) rs942061396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4988588 86932 RMVar_ID_86932 Human_SNP_ID_364182677 m1A Human chr8 - 55879971 55879971 55879971 GGCTGCTGGCCGGGAACGCTGGACGCGCGGCGAGGGGCTGCTGGCGCGGGGCCGGGGGTGGCGCG GGCTGCTGGCCGGGAACGCTGGACGCGCGGCGTGGGGCTGCTGGCGCGGGGCCGGGGGTGGCGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:55879841..55880045;chr8:55879852..55880074 26863196 MeRIP-seq:(Medium) rs1308834527 Functional Loss SNV dbSNP153 33..33 33 - - - 86933 RMVar_ID_86933 Human_SNP_ID_364182690 m1A Human chr8 - 55880004 55880004 55880004 ACGGGGCGGCCCAGCAGGACCTGCGTATGGGGAGGCTGCTGGCCGGGAACGCTGGACGCGCGGCG ACGGGGCGGCCCAGCAGGACCTGCGTATGGGGGGGCTGCTGGCCGGGAACGCTGGACGCGCGGCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:55879876..55880003 26863196 MeRIP-seq:(Medium) rs1213860710 Functional Loss SNV dbSNP153 33..33 33 - - - 86934 RMVar_ID_86934 Human_SNP_ID_364229982 m1A Human chr8 - 56073217 56073217 56073217 AACTCCTTGTGGTGAAGGTTCTAAGACGTGGGATCGTTTCCAGATGAGAATTCACAAGCGACTCA AACTCCTTGTGGTGAAGGTTCTAAGACGTGGGGTCGTTTCCAGATGAGAATTCACAAGCGACTCA T C RPS20 Ensembl:ENSG00000008988 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:56073151..56073302 32194978 MeRIP-seq:(Medium) rs1281349981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_701450,Human_RBP_ID_1698125,Human_RBP_ID_9226878,Human_RBP_ID_23216102 Human_Splice_Rec_978654,Human_Splice_Rec_978664,Human_Splice_Rec_978672,Human_Splice_Rec_978676,Human_Splice_Rec_978680,Human_Splice_Rec_978686,Human_Splice_Rec_978690,Human_Splice_Rec_978698,Human_Splice_Rec_978702 RMVar_hsa_circ_84778,RMVar_hsa_circ_96015,RMVar_hsa_circ_127905,RMVar_hsa_circ_252195,RMVar_hsa_circ_252196,RMVar_hsa_circ_252197 86935 RMVar_ID_86935 Human_SNP_ID_364230374 m1A Human chr8 + 56074043 56074043 56074043 TCGCTTTTCGCCCAATTCCCCCTCCCCCCCGCATAACGAATGCACTGACCCTTTTCCAAGGATTT TCGCTTTTCGCCCAATTCCCCCTCCCCCCCGCGTAACGAATGCACTGACCCTTTTCCAAGGATTT A G NONHSAG050272.2 RNACentral:URS00009B95B1 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:56074039..56074187 32194978 MeRIP-seq:(Medium) rs1450379932 Functional Loss SNV dbSNP153 33..33 33 - - - 86936 RMVar_ID_86936 Human_SNP_ID_364230375 m1A Human chr8 + 56074043 56074043 56074043 TCGCTTTTCGCCCAATTCCCCCTCCCCCCCGCATAACGAATGCACTGACCCTTTTCCAAGGATTT TCGCTTTTCGCCCAATTCCCCCTCCCCCCCGCTTAACGAATGCACTGACCCTTTTCCAAGGATTT A T NONHSAG050272.2 RNACentral:URS00009B95B1 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:56074039..56074187 32194978 MeRIP-seq:(Medium) rs1450379932 Functional Loss SNV dbSNP153 33..33 33 - - - 86937 RMVar_ID_86937 Human_SNP_ID_364230436 m1A Human chr8 - 56074147 56074147 56074147 TTTCATGTATCTAATAATAGGCTTTTAAGGATACCGGAAAAACACCCGTGGAGCCGGAGGTGGCA TTTCATGTATCTAATAATAGGCTTTTAAGGATGCCGGAAAAACACCCGTGGAGCCGGAGGTGGCA T C RPS20 Ensembl:ENSG00000008988 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:56074012..56074209 26863196 MeRIP-seq:(Medium) rs761123618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4988651,Human_RBP_ID_9226885,Human_RBP_ID_9405478,Human_RBP_ID_16442103,Human_RBP_ID_18124967,Human_RBP_ID_22332186,Human_RBP_ID_26832208,Human_RBP_ID_27366772 Human_Splice_Rec_978650,Human_Splice_Rec_978651,Human_Splice_Rec_978660,Human_Splice_Rec_978661,Human_Splice_Rec_978668,Human_Splice_Rec_978669,Human_Splice_Rec_978673,Human_Splice_Rec_978678,Human_Splice_Rec_978679,Human_Splice_Rec_978682,Human_Splice_Rec_978683,Human_Splice_Rec_978692,Human_Splice_Rec_978693,Human_Splice_Rec_978696,Human_Splice_Rec_978697,Human_Splice_Rec_978700,Human_Splice_Rec_978704,Human_Splice_Rec_978705,Human_Splice_Rec_978708 Human_miRNA_ID_2668786,Human_miRNA_ID_2668787 RMVar_hsa_circ_96015,RMVar_hsa_circ_127905,RMVar_hsa_circ_252195,RMVar_hsa_circ_118466,RMVar_hsa_circ_252197,RMVar_hsa_circ_363280,RMVar_hsa_circ_370472,RMVar_hsa_circ_252198,RMVar_hsa_circ_252200,RMVar_hsa_circ_101738,RMVar_hsa_circ_252199 86938 RMVar_ID_86938 Human_SNP_ID_364230437 m1A Human chr8 - 56074147 56074147 56074147 TTTCATGTATCTAATAATAGGCTTTTAAGGATACCGGAAAAACACCCGTGGAGCCGGAGGTGGCA TTTCATGTATCTAATAATAGGCTTTTAAGGATCCCGGAAAAACACCCGTGGAGCCGGAGGTGGCA T G RPS20 Ensembl:ENSG00000008988 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:56074012..56074209 26863196 MeRIP-seq:(Medium) rs761123618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4988651,Human_RBP_ID_9226885,Human_RBP_ID_9405478,Human_RBP_ID_16442103,Human_RBP_ID_18124967,Human_RBP_ID_22332186,Human_RBP_ID_26832208,Human_RBP_ID_27366772 Human_Splice_Rec_978650,Human_Splice_Rec_978651,Human_Splice_Rec_978660,Human_Splice_Rec_978661,Human_Splice_Rec_978668,Human_Splice_Rec_978669,Human_Splice_Rec_978673,Human_Splice_Rec_978678,Human_Splice_Rec_978679,Human_Splice_Rec_978682,Human_Splice_Rec_978683,Human_Splice_Rec_978692,Human_Splice_Rec_978693,Human_Splice_Rec_978696,Human_Splice_Rec_978697,Human_Splice_Rec_978700,Human_Splice_Rec_978704,Human_Splice_Rec_978705,Human_Splice_Rec_978708 Human_miRNA_ID_2668786,Human_miRNA_ID_2668787 RMVar_hsa_circ_96015,RMVar_hsa_circ_127905,RMVar_hsa_circ_252195,RMVar_hsa_circ_118466,RMVar_hsa_circ_252197,RMVar_hsa_circ_363280,RMVar_hsa_circ_370472,RMVar_hsa_circ_252198,RMVar_hsa_circ_252200,RMVar_hsa_circ_101738,RMVar_hsa_circ_252199 86939 RMVar_ID_86939 Human_SNP_ID_364230438 m1A Human chr8 + 56074148 56074148 56074148 GCCACCTCCGGCTCCACGGGTGTTTTTCCGGTATCCTTAAAAGCCTATTATTAGATACATGAAAA GCCACCTCCGGCTCCACGGGTGTTTTTCCGGTGTCCTTAAAAGCCTATTATTAGATACATGAAAA A G NONHSAG050272.2 RNACentral:URS00009B95B1 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:56074051..56074175 26863196 MeRIP-seq:(Medium) rs1804369 Functional Loss SNV dbSNP153 33..33 33 - - - 86940 RMVar_ID_86940 Human_SNP_ID_364230615 m1A Human chr8 - 56074405 56074405 56074405 GCTGTTCGCTCTCGCCGAGGAACAAGTCGGTCAGGAAGCCCGCGCGCAACAGCCATGGTGAGGCG GCTGTTCGCTCTCGCCGAGGAACAAGTCGGTCGGGAAGCCCGCGCGCAACAGCCATGGTGAGGCG T C RPS20 Ensembl:ENSG00000008988 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:56074034..56074532 26863410 MeRIP-seq:(Medium) rs917720796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87840,Human_RBP_ID_1698137,Human_RBP_ID_2056237,Human_RBP_ID_3879899,Human_RBP_ID_4988655,Human_RBP_ID_7844939,Human_RBP_ID_8688658,Human_RBP_ID_9338654,Human_RBP_ID_16442105,Human_RBP_ID_17665955,Human_RBP_ID_18897849,Human_RBP_ID_19141284,Human_RBP_ID_22465575,Human_RBP_ID_24262117,Human_RBP_ID_26556458,Human_RBP_ID_27125807,Human_RBP_ID_27366773 Human_Splice_Rec_978649,Human_Splice_Rec_978659,Human_Splice_Rec_978667,Human_Splice_Rec_978677,Human_Splice_Rec_978687,Human_Splice_Rec_978695,Human_Splice_Rec_978699,Human_Splice_Rec_978703,Human_Splice_Rec_978707 Human_miRNA_ID_2250049,Human_miRNA_ID_2250050 RMVar_hsa_circ_127905,RMVar_hsa_circ_118466,RMVar_hsa_circ_252197,RMVar_hsa_circ_363280,RMVar_hsa_circ_252200 86941 RMVar_ID_86941 Human_SNP_ID_364230616 m1A Human chr8 - 56074405 56074405 56074405 GCTGTTCGCTCTCGCCGAGGAACAAGTCGGTCAGGAAGCCCGCGCGCAACAGCCATGGTGAGGCG GCTGTTCGCTCTCGCCGAGGAACAAGTCGGTCCGGAAGCCCGCGCGCAACAGCCATGGTGAGGCG T G RPS20 Ensembl:ENSG00000008988 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:56074034..56074532 26863410 MeRIP-seq:(Medium) rs917720796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87840,Human_RBP_ID_1698137,Human_RBP_ID_2056237,Human_RBP_ID_3879899,Human_RBP_ID_4988655,Human_RBP_ID_7844939,Human_RBP_ID_8688658,Human_RBP_ID_9338654,Human_RBP_ID_16442105,Human_RBP_ID_17665955,Human_RBP_ID_18897849,Human_RBP_ID_19141284,Human_RBP_ID_22465575,Human_RBP_ID_24262117,Human_RBP_ID_26556458,Human_RBP_ID_27125807,Human_RBP_ID_27366773 Human_Splice_Rec_978649,Human_Splice_Rec_978659,Human_Splice_Rec_978667,Human_Splice_Rec_978677,Human_Splice_Rec_978687,Human_Splice_Rec_978695,Human_Splice_Rec_978699,Human_Splice_Rec_978703,Human_Splice_Rec_978707 Human_miRNA_ID_2250049,Human_miRNA_ID_2250050 RMVar_hsa_circ_127905,RMVar_hsa_circ_118466,RMVar_hsa_circ_252197,RMVar_hsa_circ_363280,RMVar_hsa_circ_252200 86942 RMVar_ID_86942 Human_SNP_ID_364230649 m1A Human chr8 + 56074452 56074452 56074452 TCGGCGAGAGCGAACAGCGGTGAGTCAGGAGCAGGAGCGTGCGGACCAAAAATCCTCAGCCCTTA TCGGCGAGAGCGAACAGCGGTGAGTCAGGAGCGGGAGCGTGCGGACCAAAAATCCTCAGCCCTTA A G NONHSAG050272.2 RNACentral:URS00009B95B1 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr8:56074276..56074500;chr8:56074101..56074500;chr8:56074191..56074500;chr8:56074126..56074532 26863196 MeRIP-seq:(Medium) rs1038847853 Functional Loss SNV dbSNP153 33..33 33 - - - 86943 RMVar_ID_86943 Human_SNP_ID_364230652 m1A Human chr8 + 56074455 56074455 56074455 GCGAGAGCGAACAGCGGTGAGTCAGGAGCAGGAGCGTGCGGACCAAAAATCCTCAGCCCTTACGA GCGAGAGCGAACAGCGGTGAGTCAGGAGCAGGGGCGTGCGGACCAAAAATCCTCAGCCCTTACGA A G NONHSAG050272.2 RNACentral:URS00009B95B1 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:56074126..56074500;chr8:56074101..56074500 26863196 MeRIP-seq:(Medium) rs777444985 Functional Loss SNV dbSNP153 33..33 33 - - - 86944 RMVar_ID_86944 Human_SNP_ID_364728502 m1A Human chr8 - 57994646 57994646 57994646 GTGTTCACGGTCGCCGCCGCGGGGCCGCGGGTAGAGAGCAGACGGGGCTGGCGGAACGGGCCCAG GTGTTCACGGTCGCCGCCGCGGGGCCGCGGGTTGAGAGCAGACGGGGCTGGCGGAACGGGCCCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:57994558..57994712 26863410 MeRIP-seq:(Medium) rs895023788 Functional Loss SNV dbSNP153 33..33 33 - - - 86945 RMVar_ID_86945 Human_SNP_ID_364763453 m1A Human chr8 + 58146684 58146684 58146684 CCCGCAACTGGCCGCCCCACCGGTCGGAAGCCACTGACCTGCACCGTCACTCCTTCGCGGAGTCC CCCGCAACTGGCCGCCCCACCGGTCGGAAGCCTCTGACCTGCACCGTCACTCCTTCGCGGAGTCC A T FAM110B Ensembl:ENSG00000169122 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:58146633..58146884 26863196 MeRIP-seq:(Medium) rs1200587504 Functional Loss SNV dbSNP153 33..33 33 - - - 86946 RMVar_ID_86946 Human_SNP_ID_364864120 m1A Human chr8 - 58553301 58553301 58553301 GCGTCCCTCCTTGCCCCCTTGGCCTCTCACCTAGCCCACAAGGAACCGCTCGCCGCCGCCGCCTC GCGTCCCTCCTTGCCCCCTTGGCCTCTCACCTGGCCCACAAGGAACCGCTCGCCGCCGCCGCCTC T C RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:58553251..58553384;chr8:58553251..58553379 26863196 MeRIP-seq:(Medium) rs1394307912 Functional Loss SNV dbSNP153 33..33 33 - - - 86947 RMVar_ID_86947 Human_SNP_ID_364864121 m1A Human chr8 + 58553302 58553302 58553302 AGGCGGCGGCGGCGAGCGGTTCCTTGTGGGCTAGGTGAGAGGCCAAGGGGGCAAGGAGGGACGCC AGGCGGCGGCGGCGAGCGGTTCCTTGTGGGCTCGGTGAGAGGCCAAGGGGGCAAGGAGGGACGCC A C SDCBP Ensembl:ENSG00000137575 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:58553251..58553391 26863196 MeRIP-seq:(Medium) rs1324318712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255347,Human_RBP_ID_4995536,Human_RBP_ID_17433857,Human_RBP_ID_22464947 Human_Splice_Rec_979735,Human_Splice_Rec_979739,Human_Splice_Rec_979755,Human_Splice_Rec_979771,Human_Splice_Rec_979787,Human_Splice_Rec_979805,Human_Splice_Rec_979819,Human_Splice_Rec_979829,Human_Splice_Rec_979845 86948 RMVar_ID_86948 Human_SNP_ID_364865906 m1A Human chr8 - 58560554 58560554 58560554 TGCTGCAAGCCACCCAGCTCTCTTGTTTTCAGAGGCCTCCAACCTGGTGCCCTTTCCCATCAGTG TGCTGCAAGCCACCCAGCTCTCTTGTTTTCAGTGGCCTCCAACCTGGTGCCCTTTCCCATCAGTG T A RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:58560550..58560650 32194978 MeRIP-seq:(Medium) rs549823124 Functional Loss SNV dbSNP153 33..33 33 - - - 86949 RMVar_ID_86949 Human_SNP_ID_364866786 m1A Human chr8 - 58565004 58565000 58565004 CATTTTTGCAGGATTCTTCTAAAGAAAAAAAGAAAGTTTTATTACTCTAATGTCATAGAAATTGA CATTTTTGCAGGATTCTTCTAAAGAAAAAAAG____TTTTATTACTCTAATGTCATAGAAATTGA ACTTT A RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:58565001..58565100 26863196 MeRIP-seq:(Medium) rs750444817 Functional Loss DEL dbSNP153 33..36 33 - - - 86950 RMVar_ID_86950 Human_SNP_ID_364866786 m1A Human chr8 - 58565003 58565000 58565004 ATTTTTGCAGGATTCTTCTAAAGAAAAAAAGAAAGTTTTATTACTCTAATGTCATAGAAATTGAA ATTTTTGCAGGATTCTTCTAAAGAAAAAAAG____TTTTATTACTCTAATGTCATAGAAATTGAA ACTTT A RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:58565001..58565100 26863196 MeRIP-seq:(Medium) rs750444817 Functional Loss DEL dbSNP153 32..35 33 - - - 86951 RMVar_ID_86951 Human_SNP_ID_364866787 m1A Human chr8 - 58565003 58565001 58565003 ATTTTTGCAGGATTCTTCTAAAGAAAAAAAGAAAGTTTTATTACTCTAATGTCATAGAAATTGAA ATTTTTGCAGGATTCTTCTAAAGAAAAAAAGA__GTTTTATTACTCTAATGTCATAGAAATTGAA CTT C RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:58565001..58565100 26863196 MeRIP-seq:(Medium) rs1249571345 Functional Loss DEL dbSNP153 33..34 33 - - - 86952 RMVar_ID_86952 Human_SNP_ID_364866788 m1A Human chr8 - 58565004 58565004 58565004 CATTTTTGCAGGATTCTTCTAAAGAAAAAAAGAAAGTTTTATTACTCTAATGTCATAGAAATTGA CATTTTTGCAGGATTCTTCTAAAGAAAAAAAGGAAGTTTTATTACTCTAATGTCATAGAAATTGA T C RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:58565001..58565100 26863196 MeRIP-seq:(Medium) rs1563507112 Functional Loss SNV dbSNP153 33..33 33 - - - 86953 RMVar_ID_86953 Human_SNP_ID_364868035 m1A Human chr8 + 58570825 58570825 58570825 TTCTTTTTGGAAGTACTGGATTTAGCTTATAAATTATATAAGAATATAAAGTAAGTATAGCATAT TTCTTTTTGGAAGTACTGGATTTAGCTTATAAGTTATATAAGAATATAAAGTAAGTATAGCATAT A G SDCBP Ensembl:ENSG00000137575 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:58570818..58570950 26863410 MeRIP-seq:(Medium) rs543059153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3163006 RMVar_hsa_circ_39845,RMVar_hsa_circ_25921,RMVar_hsa_circ_39496,RMVar_hsa_circ_313585,RMVar_hsa_circ_16726,RMVar_hsa_circ_252215 86954 RMVar_ID_86954 Human_SNP_ID_364870687 m1A Human chr8 - 58582260 58582260 58582260 AGAATCATCACAATCTCTTGAAACCTACATACACTGTTTAATGCTTACATGGAATGAAACCAGTG AGAATCATCACAATCTCTTGAAACCTACATACCCTGTTTAATGCTTACATGGAATGAAACCAGTG T G RF00017-4567 RNACentral:URS000094CDE3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:58582162..58582313 32194978 MeRIP-seq:(Medium) rs117089964 Functional Loss SNV dbSNP153 33..33 33 - - - 86955 RMVar_ID_86955 Human_SNP_ID_364882252 m1A Human chr8 - 58629101 58629101 58629101 AGAAAGAAACAGAAAGTGTATTTAAAGAGATAATGGCCCCAAACTTGCCAAAACAGAGGAAGGAG AGAAAGAAACAGAAAGTGTATTTAAAGAGATAGTGGCCCCAAACTTGCCAAAACAGAGGAAGGAG T C NSMAF Ensembl:ENSG00000035681 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:58629097..58629232 26863196 MeRIP-seq:(Medium) rs963375417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22530066,Human_RBP_ID_26359913 RMVar_hsa_circ_48015,RMVar_hsa_circ_252226,RMVar_hsa_circ_47908,RMVar_hsa_circ_252223,RMVar_hsa_circ_72090,RMVar_hsa_circ_77792,RMVar_hsa_circ_96922,RMVar_hsa_circ_265086,RMVar_hsa_circ_302278,RMVar_hsa_circ_292226,RMVar_hsa_circ_93228,RMVar_hsa_circ_252228,RMVar_hsa_circ_252229,RMVar_hsa_circ_252227,RMVar_hsa_circ_252224,RMVar_hsa_circ_252225,RMVar_hsa_circ_300023 86956 RMVar_ID_86956 Human_SNP_ID_364884278 m1A Human chr8 + 58638147 58638147 58638147 TTATAGCTCACTGCAGCCTCAAAATGGGCTCAATCAATCCTCCTGCTTCAGCTTTCCAAGTAGCT TTATAGCTCACTGCAGCCTCAAAATGGGCTCAGTCAATCCTCCTGCTTCAGCTTTCCAAGTAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:58638142..58638226 26863196 MeRIP-seq:(Medium) rs1203741807 Functional Loss SNV dbSNP153 33..33 33 - - - 86957 RMVar_ID_86957 Human_SNP_ID_364999423 m1A Human chr8 + 59118991 59118991 59118991 GCTGGAGGTGGATAAAATCTTACGTCCATTTCACTCTCACATCAAGCAACTCCTTTTCTTTTTCC GCTGGAGGTGGATAAAATCTTACGTCCATTTCGCTCTCACATCAAGCAACTCCTTTTCTTTTTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:59118948..59119090 26863196 MeRIP-seq:(Medium) rs747716822 Functional Loss SNV dbSNP153 33..33 33 - - - 86958 RMVar_ID_86958 Human_SNP_ID_364999507 m1A Human chr8 + 59119237 59119223 59119238 CACCCGTCGGCGCCGAGCGCGCAGCCTGCTCCACCGCCGCCTCTTGGTCCCGCCGCCGCCGCTGC CACCCGTCGGCGCCGAGCG_______________CGCCGCCTCTTGGTCCCGCCGCCGCCGCTGC GCGCAGCCTGCTCCAC G AC090152.1 Ensembl:ENSG00000167912 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:59119191..59119322 26863196 MeRIP-seq:(Medium) rs1374857070 Functional Loss DEL dbSNP153 20..34 33 - - - Human_Splice_Rec_980225,Human_Splice_Rec_980227,Human_Splice_Rec_980229 86959 RMVar_ID_86959 Human_SNP_ID_364999690 m1A Human chr8 + 59119623 59119620 59119623 GGGGACCGGAGAAAGGAGGAGCGGAGAAGGAGAAGGAGGAGAGCACGGCCTGGCTGGGACAGAAG GGGGACCGGAGAAAGGAGGAGCGGAGAAGG___AGGAGGAGAGCACGGCCTGGCTGGGACAGAAG GAGA G AC090152.1 Ensembl:ENSG00000167912 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:59119238..59119738 26863196 MeRIP-seq:(Medium) rs901210776 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_980226 86960 RMVar_ID_86960 Human_SNP_ID_364999691 m1A Human chr8 + 59119623 59119623 59119623 GGGGACCGGAGAAAGGAGGAGCGGAGAAGGAGAAGGAGGAGAGCACGGCCTGGCTGGGACAGAAG GGGGACCGGAGAAAGGAGGAGCGGAGAAGGAGGAGGAGGAGAGCACGGCCTGGCTGGGACAGAAG A G AC090152.1 Ensembl:ENSG00000167912 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:59119238..59119738 26863196 MeRIP-seq:(Medium) rs1024429048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_980226 86961 RMVar_ID_86961 Human_SNP_ID_364999815 m1A Human chr8 - 59119932 59119932 59119932 CACCTCCACTACGGGCCGGGAGTAGGGAGGGGAGCACAGTGACAGGGTTGGGGAACAGCCGAGGA CACCTCCACTACGGGCCGGGAGTAGGGAGGGGGGCACAGTGACAGGGTTGGGGAACAGCCGAGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:59119886..59119987 26863196 MeRIP-seq:(Medium) rs966929685 Functional Loss SNV dbSNP153 33..33 33 - - - 86962 RMVar_ID_86962 Human_SNP_ID_131413010 m1A Human chr3 - 45007529 45007529 45007529 AGATGCTCTCTGGGTCCAGGCTGCCCTTCCCCACTTTCCTCATGCACGTCACAACTCCCTTGCTG AGATGCTCTCTGGGTCCAGGCTGCCCTTCCCCGCTTTCCTCATGCACGTCACAACTCCCTTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:45007481..45007603 26863196 MeRIP-seq:(Medium) rs780882326 Functional Loss SNV dbSNP153 33..33 33 - - - 86963 RMVar_ID_86963 Human_SNP_ID_131413975 m1A Human chr3 + 45011351 45011351 45011351 AAAGTTGGATTCCTGGGATGATTTGCACATCAACTGCTCAACTGTGGATTGTTTTTTACTTTTCC AAAGTTGGATTCCTGGGATGATTTGCACATCAGCTGCTCAACTGTGGATTGTTTTTTACTTTTCC A G CLEC3B,EXOSC7 Ensembl:ENSG00000163815,Ensembl:ENSG00000075914 Protein coding,Protein coding intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:45011301..45011425 32194978 MeRIP-seq:(Medium) rs188532189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602502,Human_RBP_ID_1963245,Human_RBP_ID_2785640,Human_RBP_ID_9140969,Human_RBP_ID_14830081,Human_RBP_ID_17290286,Human_RBP_ID_17403635,Human_RBP_ID_17520063,Human_RBP_ID_18808790,Human_RBP_ID_22089647,Human_RBP_ID_24004012,Human_RBP_ID_26684916 Human_Splice_Rec_419003,Human_Splice_Rec_419049,Human_Splice_Rec_419065,Human_Splice_Rec_419077 RMVar_hsa_circ_368299,RMVar_hsa_circ_217386,RMVar_hsa_circ_78302,RMVar_hsa_circ_95227,RMVar_hsa_circ_217394,RMVar_hsa_circ_217395 86964 RMVar_ID_86964 Human_SNP_ID_131417659 m1A Human chr3 + 45026448 45026448 45026448 GGTCACCACCGAGCCACCAACCCAGAAGCCCAAGAAGATTGTAAATGCCAAGAAAGGTAAGGAGG GGTCACCACCGAGCCACCAACCCAGAAGCCCAGGAAGATTGTAAATGCCAAGAAAGGTAAGGAGG A G CLEC3B,EXOSC7 Ensembl:ENSG00000163815,Ensembl:ENSG00000075914 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:45026324..45026466 26863196 MeRIP-seq:(Medium) rs1168368782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_419085 86965 RMVar_ID_86965 Human_SNP_ID_131446255 m1A Human chr3 + 45146363 45146363 45146363 GAGCGGCGGCCCCAGGCGCCCAAGCCCGGCGCAGCTGCGCTCCGCCCTGGCTCACTCACCTGCGC GAGCGGCGGCCCCAGGCGCCCAAGCCCGGCGCGGCTGCGCTCCGCCCTGGCTCACTCACCTGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45146314..45146381 26863196 MeRIP-seq:(Medium) rs1280517644 Functional Loss SNV dbSNP153 33..33 33 - - - 86966 RMVar_ID_86966 Human_SNP_ID_131465358 m1A Human chr3 + 45225049 45225049 45225049 AAGAGGAACTAACGATAACTACAGCACGAAGCACACCGGCCGAGTCTCCGGCGGGAAAGGCACCC AAGAGGAACTAACGATAACTACAGCACGAAGCGCACCGGCCGAGTCTCCGGCGGGAAAGGCACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:45224998..45225260 26863196 MeRIP-seq:(Medium) rs970836753 Functional Loss SNV dbSNP153 33..33 33 - - - 86967 RMVar_ID_86967 Human_SNP_ID_131465702 m1A Human chr3 + 45225984 45225959 45225984 GCGCGTCCGCGGCCCCGCCGCGGACGGGCGGCAGCGGGCAGGCGGCGGCCAGGAGCGCGGCGAGC GCGCGTCC_________________________GCGGGCAGGCGGCGGCCAGGAGCGCGGCGAGC CGCGGCCCCGCCGCGGACGGGCGGCA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:45225934..45226194 32194978 MeRIP-seq:(Medium) rs971555614 Functional Loss DEL dbSNP153 9..33 33 - - - 86968 RMVar_ID_86968 Human_SNP_ID_131465735 m1A Human chr3 + 45226086 45226086 45226086 GAGGCCGGCGGCGGTTGCATGGCGAGCGGGCGACGGGCCGGCGAGCTCACGGTGGGACCGCGGGA GAGGCCGGCGGCGGTTGCATGGCGAGCGGGCGGCGGGCCGGCGAGCTCACGGTGGGACCGCGGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr3:45225818..45226287;chr3:45225918..45226273 26863196 MeRIP-seq:(Medium) rs1338941634 Functional Loss SNV dbSNP153 33..33 33 - - - 86969 RMVar_ID_86969 Human_SNP_ID_131503403 m1A Human chr3 + 45388679 45388658 45388679 AGTAGAGGAGCCGCAGGCCAGAGCCTGTGAGCAGGTAAACCCCCGGACCGGGCGCAGCGAGATGA AGTAGAGGAGCC_____________________GGTAAACCCCCGGACCGGGCGCAGCGAGATGA CGCAGGCCAGAGCCTGTGAGCA C LARS2 Ensembl:ENSG00000011376 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:45388640..45388739 26863196 MeRIP-seq:(Medium) rs1169996322 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_8874931,Human_RBP_ID_19010039,Human_RBP_ID_26346734 Human_Splice_Rec_419119,Human_Splice_Rec_419159,Human_Splice_Rec_419197,Human_Splice_Rec_419241,Human_Splice_Rec_419251,Human_Splice_Rec_419293,Human_Splice_Rec_419335,Human_Splice_Rec_419377 RMVar_hsa_circ_89849,RMVar_hsa_circ_217402,RMVar_hsa_circ_80401,RMVar_hsa_circ_217401 86970 RMVar_ID_86970 Human_SNP_ID_131549582 m1A Human chr3 + 45594216 45594216 45594216 CGCGCGCGCCGATCCGCCGCCGCCATCGGACAATGGGCCGCCAGCCCCAGCTGCCGTGAACTTCC CGCGCGCGCCGATCCGCCGCCGCCATCGGACAGTGGGCCGCCAGCCCCAGCTGCCGTGAACTTCC A G LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:45594137..45594429;chr3:45594168..45594400 26863196 MeRIP-seq:(Medium) rs886394091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757148,Human_RBP_ID_5530315,Human_RBP_ID_18808851 86971 RMVar_ID_86971 Human_SNP_ID_131555934 m1A Human chr3 - 45618496 45618495 45618496 ACACCCACATTCCACACACTGCACTTCACAAAACCTCCTGAGTTCTTCCCCAGGCCTCCCAGACT ACACCCACATTCCACACACTGCACTTCACAAA_CCTCCTGAGTTCTTCCCCAGGCCTCCCAGACT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45618475..45618606 26863196 MeRIP-seq:(Medium) rs144206464 Functional Loss DEL dbSNP153 33..33 33 - - - 86972 RMVar_ID_86972 Human_SNP_ID_131559037 m1A Human chr3 + 45631585 45631585 45631585 TCACGGTGGAGAGAAAGGATGTCAGCAGCCCGAAGGACTCAGCTGCAGGAACAGAAAGTGAGGGA TCACGGTGGAGAGAAAGGATGTCAGCAGCCCGGAGGACTCAGCTGCAGGAACAGAAAGTGAGGGA A G LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45631572..45631673 26863196 MeRIP-seq:(Medium) rs940126414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324991,RMVar_hsa_circ_346287 86973 RMVar_ID_86973 Human_SNP_ID_131564137 m1A Human chr3 + 45653239 45653239 45653239 AGAAGGAAGGAGTGATGTAGGGGATTTGGATGAGGAGGGAGAGAGGGTGGTGGTTATGATTCTTA AGAAGGAAGGAGTGATGTAGGGGATTTGGATGTGGAGGGAGAGAGGGTGGTGGTTATGATTCTTA A T LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45653236..45653367 26863196 MeRIP-seq:(Medium) rs1172273624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340076,RMVar_hsa_circ_346287,RMVar_hsa_circ_99368,RMVar_hsa_circ_217431,RMVar_hsa_circ_32682 86974 RMVar_ID_86974 Human_SNP_ID_131570423 m1A Human chr3 + 45680041 45680041 45680041 ATGGAATGATTGAGGAGGTCTGGTCACCCTCAAGCGCCGTCATCGCCTTGTTTCCATGGGCTTCT ATGGAATGATTGAGGAGGTCTGGTCACCCTCAGGCGCCGTCATCGCCTTGTTTCCATGGGCTTCT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:45679851..45680052 32194978 MeRIP-seq:(Medium) rs1186462098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8573138,Human_RBP_ID_17573402,Human_RBP_ID_18012788 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86975 RMVar_ID_86975 Human_SNP_ID_131570494 m1A Human chr3 + 45680344 45680340 45680344 TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG TTCTTTTCTTTTTTTTTTTGAGACAGGGC____CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG CCTCA C LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs566830328 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86976 RMVar_ID_86976 Human_SNP_ID_131570496 m1A Human chr3 + 45680344 45680344 45680344 TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1420439251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86977 RMVar_ID_86977 Human_SNP_ID_131570539 m1A Human chr3 + 45680497 45680497 45680497 ACTGGCTACGCCTGGCTAATTTTTGTATTTTTAATAGAGACGAGTTTCACCATGTTGCCCAGGAT ACTGGCTACGCCTGGCTAATTTTTGTATTTTTGATAGAGACGAGTTTCACCATGTTGCCCAGGAT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1475053982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14833726 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86978 RMVar_ID_86978 Human_SNP_ID_131570654 m1A Human chr3 + 45680916 45680916 45680916 CCTGTAATCCCAGCTACCTGAGAGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACCTGAGAGGTTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCAGAGGTT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1254048879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86979 RMVar_ID_86979 Human_SNP_ID_131570665 m1A Human chr3 + 45680938 45680937 45680938 AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA AGGTTGAGGCAGGAGAATCGCTTGAACCTGGG_GGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA GA G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1397969557 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86980 RMVar_ID_86980 Human_SNP_ID_131570666 m1A Human chr3 + 45680938 45680938 45680938 AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGGGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs944039583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 86981 RMVar_ID_86981 Human_SNP_ID_131573022 m1A Human chr3 + 45689463 45689463 45689463 GGGCGGAGAGAGAAGGAAGGAGGTGGTTGTGCAGGATGGCGACGGCGGCCTACGAGCAGCTGAAG GGGCGGAGAGAGAAGGAAGGAGGTGGTTGTGCGGGATGGCGACGGCGGCCTACGAGCAGCTGAAG A G SACM1L Ensembl:ENSG00000211456 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45689351..45689569 26863196 MeRIP-seq:(Medium) rs1225525733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248682,Human_RBP_ID_266406,Human_RBP_ID_3963845,Human_RBP_ID_4742942,Human_RBP_ID_5149673,Human_RBP_ID_5325200,Human_RBP_ID_9434842,Human_RBP_ID_18423958,Human_RBP_ID_23288114,Human_RBP_ID_24004303,Human_RBP_ID_26790288,Human_RBP_ID_27841376 Human_Splice_Rec_419555,Human_Splice_Rec_419591,Human_Splice_Rec_419601,Human_Splice_Rec_419635,Human_Splice_Rec_419667,Human_Splice_Rec_419673,Human_Splice_Rec_419683,Human_Splice_Rec_419717,Human_Splice_Rec_419725,Human_Splice_Rec_419737 86982 RMVar_ID_86982 Human_SNP_ID_131573030 m1A Human chr3 - 45689481 45689481 45689481 GGCCCGTGGGACTCACAGCTTCAGCTGCTCGTAGGCCGCCGTCGCCATCCTGCACAACCACCTCC GGCCCGTGGGACTCACAGCTTCAGCTGCTCGTGGGCCGCCGTCGCCATCCTGCACAACCACCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:45689351..45689653;chr3:45689333..45689653 26863196 MeRIP-seq:(Medium) rs763837572 Functional Loss SNV dbSNP153 33..33 33 - - - 86983 RMVar_ID_86983 Human_SNP_ID_131576528 m1A Human chr3 - 45703489 45703489 45703489 TCTGTGGACACACGGTCAATGGTAAGTACGTCATCTGCTCCATCATCACAAGCTTCCACATAAAA TCTGTGGACACACGGTCAATGGTAAGTACGTCGTCTGCTCCATCATCACAAGCTTCCACATAAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:45703395..45703525;chr3:45703393..45703550 26863196 MeRIP-seq:(Medium) rs768481910 Functional Loss SNV dbSNP153 33..33 33 - - - 86984 RMVar_ID_86984 Human_SNP_ID_131584539 m1A Human chr3 - 45737176 45737176 45737176 ATCCCTCAACTTCTTCACCCCTGAGTCACCCCAGCCTTACCCTCTGTCCCAGGGACCTTTAAGAA ATCCCTCAACTTCTTCACCCCTGAGTCACCCCGGCCTTACCCTCTGTCCCAGGGACCTTTAAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45736966..45737230 26863196 MeRIP-seq:(Medium) rs188646503 Functional Loss SNV dbSNP153 33..33 33 - - - 86985 RMVar_ID_86985 Human_SNP_ID_131606955 m1A Human chr3 + 45831786 45831786 45831786 ACAATTTAACTGGTCTTCATCCTTCAAGGCCCAGCTTAGGTACCCCTTTACCCAAGAGCCTGTTC ACAATTTAACTGGTCTTCATCCTTCAAGGCCCGGCTTAGGTACCCCTTTACCCAAGAGCCTGTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:45831738..45831824 26863196 MeRIP-seq:(Medium) rs1428130927 Functional Loss SNV dbSNP153 33..33 33 - - - 86986 RMVar_ID_86986 Human_SNP_ID_131606956 m1A Human chr3 + 45831786 45831786 45831786 ACAATTTAACTGGTCTTCATCCTTCAAGGCCCAGCTTAGGTACCCCTTTACCCAAGAGCCTGTTC ACAATTTAACTGGTCTTCATCCTTCAAGGCCCTGCTTAGGTACCCCTTTACCCAAGAGCCTGTTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:45831738..45831824 26863196 MeRIP-seq:(Medium) rs1428130927 Functional Loss SNV dbSNP153 33..33 33 - - - 86987 RMVar_ID_86987 Human_SNP_ID_131636849 m1A Human chr3 - 45966332 45966331 45966333 GAGCCTCCAAGAGGCTGCACACCAGGAGCTCAACACCCTCAAGTTCCAGCTGAGTGCTGAAATCA GAGCCTCCAAGAGGCTGCACACCAGGAGCTCGAAACCCTCAAGTTCCAGCTGAGTGCTGAAATCA GTT TTC FYCO1 Ensembl:ENSG00000163820 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:45964346..45966875 32194978 MeRIP-seq:(Medium) rs71622515 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_18808991 Human_Splice_Rec_420111,Human_Splice_Rec_420147 Clinvar_Rec_470 RMVar_hsa_circ_266342,RMVar_hsa_circ_113909,RMVar_hsa_circ_217458 86988 RMVar_ID_86988 Human_SNP_ID_131636995 m1A Human chr3 - 45966662 45966662 45966662 CAAATGCAGCTCCGAGGAAGCACAGCTGGAGCACGCTGAGCTGCAAGAGCAGCTGCACCGGGCCA CAAATGCAGCTCCGAGGAAGCACAGCTGGAGCGCGCTGAGCTGCAAGAGCAGCTGCACCGGGCCA T C FYCO1 Ensembl:ENSG00000163820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45966613..45966783 26863196 MeRIP-seq:(Medium) rs754392183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530326,Human_RBP_ID_26346745 Human_miRNA_ID_206090,Human_miRNA_ID_1490259,Human_miRNA_ID_2757999 RMVar_hsa_circ_266342,RMVar_hsa_circ_113909,RMVar_hsa_circ_217458 86989 RMVar_ID_86989 Human_SNP_ID_131637492 m1A Human chr3 + 45967874 45967874 45967874 GTTGCTGTTTTTTCTCCCGCCTCAACTCTGCTAGCTCCTCCTCCCAGGAGCTCGTGTGGGCCAGC GTTGCTGTTTTTTCTCCCGCCTCAACTCTGCTCGCTCCTCCTCCCAGGAGCTCGTGTGGGCCAGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:45967823..45968043 26863196 MeRIP-seq:(Medium) rs1168880899 Functional Loss SNV dbSNP153 33..33 33 - - - 86990 RMVar_ID_86990 Human_SNP_ID_131637716 m1A Human chr3 - 45968504 45968504 45968504 TGTCAGCCAGCAAGGGGAGCAACTGCAGACAGAGAGGGAGAGGGGGCGCACTGCAGCGGAGGACA TGTCAGCCAGCAAGGGGAGCAACTGCAGACAGGGAGGGAGAGGGGGCGCACTGCAGCGGAGGACA T C FYCO1 Ensembl:ENSG00000163820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45968453..45968591 26863196 MeRIP-seq:(Medium) rs777273112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836832,Human_RBP_ID_933035,Human_RBP_ID_5530332 RMVar_hsa_circ_266342,RMVar_hsa_circ_113909,RMVar_hsa_circ_217458 86991 RMVar_ID_86991 Human_SNP_ID_131637739 m1A Human chr3 + 45968567 45968567 45968567 CAGCTGCCCTCAGCTCCTGGTTCTCTCTGTCCAGCTGCTGCATGCGCTCCCGTAGCTGCTTCTCC CAGCTGCCCTCAGCTCCTGGTTCTCTCTGTCCTGCTGCTGCATGCGCTCCCGTAGCTGCTTCTCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:45968517..45968616 26863196 MeRIP-seq:(Medium) rs1274925377 Functional Loss SNV dbSNP153 33..33 33 - - - 86992 RMVar_ID_86992 Human_SNP_ID_131642726 m1A Human chr3 - 45991611 45991611 45991611 CCTCCTGTCCACACCAAACCCAGCGAGACTGGAGCAGCTGGCCAAAGGAAGGTGTAGGGAGCATG CCTCCTGTCCACACCAAACCCAGCGAGACTGGGGCAGCTGGCCAAAGGAAGGTGTAGGGAGCATG T C FYCO1 Ensembl:ENSG00000163820 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:45991609..45991738 26863196 MeRIP-seq:(Medium) rs1197336953 Functional Loss SNV dbSNP153 33..33 33 - - - 86993 RMVar_ID_86993 Human_SNP_ID_131681496 m1A Human chr3 - 46163544 46163544 46163544 GCAGACTCCTTCTTTAAGTGGGACCCTGATCCACTCCTGCTCACTGGGCTGGACTTCCCATCCGG GCAGACTCCTTCTTTAAGTGGGACCCTGATCCGCTCCTGCTCACTGGGCTGGACTTCCCATCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46163501..46163744 26863196 MeRIP-seq:(Medium) rs972975472 Functional Loss SNV dbSNP153 33..33 33 - - - 86994 RMVar_ID_86994 Human_SNP_ID_131681502 m1A Human chr3 - 46163572 46163572 46163572 ACAACACAGCTGCTTTACCAAAATGTGGGCAGACTCCTTCTTTAAGTGGGACCCTGATCCACTCC ACAACACAGCTGCTTTACCAAAATGTGGGCAGGCTCCTTCTTTAAGTGGGACCCTGATCCACTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:46163525..46163606 26863196 MeRIP-seq:(Medium) rs558839328 Functional Loss SNV dbSNP153 33..33 33 - - - 86995 RMVar_ID_86995 Human_SNP_ID_131809206 m1A Human chr3 - 46681327 46681327 46681327 GCACGGATTTGGGGTCCTTGAGAGTGGTCCGCAGGCCCCCCAGCCCTTCAGGTACACGGGCCACT GCACGGATTTGGGGTCCTTGAGAGTGGTCCGCCGGCCCCCCAGCCCTTCAGGTACACGGGCCACT T G ALS2CL Ensembl:ENSG00000178038 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46681280..46681362 26863196 MeRIP-seq:(Medium) rs369892563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_420562,Human_Splice_Rec_420563,Human_Splice_Rec_420628,Human_Splice_Rec_420629,Human_Splice_Rec_420678,Human_Splice_Rec_420679,Human_Splice_Rec_420748,Human_Splice_Rec_420790,Human_Splice_Rec_420826,Human_Splice_Rec_420827 RMVar_hsa_circ_57807,RMVar_hsa_circ_116435,RMVar_hsa_circ_217465 86996 RMVar_ID_86996 Human_SNP_ID_131809486 m1A Human chr3 - 46682096 46682096 46682096 GGCCTGAGGCTCGTGAACCTCCACTGTGTTCCAGGGGAACCCTGAAATGGCCGGATGGGCGGAAT GGCCTGAGGCTCGTGAACCTCCACTGTGTTCCGGGGGAACCCTGAAATGGCCGGATGGGCGGAAT T C ALS2CL Ensembl:ENSG00000178038 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:46682007..46682216 26863196 MeRIP-seq:(Medium) rs776375571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_420559,Human_Splice_Rec_420625,Human_Splice_Rec_420675,Human_Splice_Rec_420745,Human_Splice_Rec_420787,Human_Splice_Rec_420823 RMVar_hsa_circ_57807,RMVar_hsa_circ_116435,RMVar_hsa_circ_217465,RMVar_hsa_circ_217466,RMVar_hsa_circ_111852 86997 RMVar_ID_86997 Human_SNP_ID_131812545 m1A Human chr3 - 46693673 46693673 46693673 GGGTGGGGGTGCGAGCGAGGAGCCGCACAGGCAGTCCCGGCGCGGGGCAACCACAGCGCTCAGGT GGGTGGGGGTGCGAGCGAGGAGCCGCACAGGCCGTCCCGGCGCGGGGCAACCACAGCGCTCAGGT T G ALS2CL Ensembl:ENSG00000178038 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:46693605..46693690 26863196 MeRIP-seq:(Medium) rs1217708999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_420539,Human_Splice_Rec_420605,Human_Splice_Rec_420725,Human_Splice_Rec_420767 86998 RMVar_ID_86998 Human_SNP_ID_131854732 m1A Human chr3 - 46882060 46882060 46882060 AGTCTTACGGCGGCGGGATGTGAGTGCTGGGGAGACGGGGCGGGGGCAGCTGTAACATCGAGACC AGTCTTACGGCGGCGGGATGTGAGTGCTGGGGGGACGGGGCGGGGGCAGCTGTAACATCGAGACC T C MYL3 Ensembl:ENSG00000160808 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:46882037..46882164 26863196 MeRIP-seq:(Medium) rs1012354461 Functional Loss SNV dbSNP153 33..33 33 - - - 86999 RMVar_ID_86999 Human_SNP_ID_131857186 m1A Human chr3 - 46891732 46891732 46891732 ATCACCACCATCTGCACCATCACAACTGGTACATCACCAGCACCAGCACCACTGCCACCACCTCC ATCACCACCATCTGCACCATCACAACTGGTACCTCACCAGCACCAGCACCACTGCCACCACCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46891730..46891907 26863196 MeRIP-seq:(Medium) rs551899776 Functional Loss SNV dbSNP153 33..33 33 - - - 87000 RMVar_ID_87000 Human_SNP_ID_131865491 m1A Human chr3 + 46923359 46923359 46923359 ACCAGTCAGGCTTCCGAGGAGCGAGGTTGGCCAGGTCCTGGGAAGGGAGGAGACACACATCAGGG ACCAGTCAGGCTTCCGAGGAGCGAGGTTGGCCGGGTCCTGGGAAGGGAGGAGACACACATCAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46923326..46923375 26863196 MeRIP-seq:(Medium) rs1207022697 Functional Loss SNV dbSNP153 33..33 33 - - - 87001 RMVar_ID_87001 Human_SNP_ID_131869839 m1A Human chr3 - 46941061 46941061 46941061 GCTGGTGGTTTTCTCCCTTTCTTTGCAGGACAAGGAAGATGGGGAGCCAAAGACCAAGCATCTCA GCTGGTGGTTTTCTCCCTTTCTTTGCAGGACAGGGAAGATGGGGAGCCAAAGACCAAGCATCTCA T C CCDC12 Ensembl:ENSG00000160799 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:46940976..46941075 26863196 MeRIP-seq:(Medium) rs1207394612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68141,Human_RBP_ID_5654592,Human_RBP_ID_9394847,Human_RBP_ID_22677717,Human_RBP_ID_24547250,Human_RBP_ID_26346764,Human_RBP_ID_27822161 Human_Splice_Rec_421274,Human_Splice_Rec_421275,Human_Splice_Rec_421288,Human_Splice_Rec_421289,Human_Splice_Rec_421300,Human_Splice_Rec_421301,Human_Splice_Rec_421310,Human_Splice_Rec_421311,Human_Splice_Rec_421316,Human_Splice_Rec_421317,Human_Splice_Rec_421326,Human_Splice_Rec_421327,Human_Splice_Rec_421332,Human_Splice_Rec_421333,Human_Splice_Rec_421336,Human_Splice_Rec_421337,Human_Splice_Rec_421342,Human_Splice_Rec_421343,Human_Splice_Rec_421348,Human_Splice_Rec_421349,Human_Splice_Rec_421352 RMVar_hsa_circ_61217,RMVar_hsa_circ_86180,RMVar_hsa_circ_111160,RMVar_hsa_circ_217471,RMVar_hsa_circ_217472,RMVar_hsa_circ_53713 87002 RMVar_ID_87002 Human_SNP_ID_131874787 m1A Human chr3 - 46961061 46961061 46961061 TCCCTTAACCTCACAACACCACCACACACCCCAGGCCCTACCCCACACACTTCCCCCCACAATAG TCCCTTAACCTCACAACACCACCACACACCCCCGGCCCTACCCCACACACTTCCCCCCACAATAG T G CCDC12 Ensembl:ENSG00000160799 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:46961059..46961220 26863196 MeRIP-seq:(Medium) rs560697508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111160,RMVar_hsa_circ_217471 87003 RMVar_ID_87003 Human_SNP_ID_131878896 m1A Human chr3 - 46976547 46976546 46976548 GCGCTTGAGGAGAGCAAAGGGCTAATAAGGAAAGACAGCTGCCGAGGGCGCGCATGCGCGGGCGC GCGCTTGAGGAGAGCAAAGGGCTAATAAGGA__GACAGCTGCCGAGGGCGCGCATGCGCGGGCGC CTT C CCDC12 Ensembl:ENSG00000160799 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:46976545..46976700 26863196 MeRIP-seq:(Medium) rs1404578961 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8124544,Human_RBP_ID_14838284,Human_RBP_ID_18499664,Human_RBP_ID_23288081 RMVar_hsa_circ_111160,RMVar_hsa_circ_217471 87004 RMVar_ID_87004 Human_SNP_ID_131878904 m1A Human chr3 - 46976567 46976567 46976567 CAGCGTTCGGGGTCCGGGTCGCGCTTGAGGAGAGCAAAGGGCTAATAAGGAAAGACAGCTGCCGA CAGCGTTCGGGGTCCGGGTCGCGCTTGAGGAGCGCAAAGGGCTAATAAGGAAAGACAGCTGCCGA T G CCDC12 Ensembl:ENSG00000160799 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:46976565..46976750 26863196 MeRIP-seq:(Medium) rs1236895642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8124544,Human_RBP_ID_9348808,Human_RBP_ID_14838284,Human_RBP_ID_18499664,Human_RBP_ID_22363579,Human_RBP_ID_23288081 RMVar_hsa_circ_111160,RMVar_hsa_circ_217471 87005 RMVar_ID_87005 Human_SNP_ID_131878964 m1A Human chr3 - 46976698 46976698 46976698 GGAGGCAACTACGGCTGGTGTGGGCCGGCTAGAGGAAGAGGCGTTGCGGCGAAAGGAACGGCTGA GGAGGCAACTACGGCTGGTGTGGGCCGGCTAGTGGAAGAGGCGTTGCGGCGAAAGGAACGGCTGA T A CCDC12 Ensembl:ENSG00000160799 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46976364..46976793 26863196 MeRIP-seq:(Medium) rs1407025982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68143,Human_RBP_ID_836911,Human_RBP_ID_4743153,Human_RBP_ID_5390667,Human_RBP_ID_9393491,Human_RBP_ID_26346765,Human_RBP_ID_27822162 Human_Splice_Rec_421273,Human_Splice_Rec_421287,Human_Splice_Rec_421309,Human_Splice_Rec_421325,Human_Splice_Rec_421331,Human_Splice_Rec_421346,Human_Splice_Rec_421347,Human_Splice_Rec_421351,Human_Splice_Rec_421354 RMVar_hsa_circ_64316,RMVar_hsa_circ_111160,RMVar_hsa_circ_217471 87006 RMVar_ID_87006 Human_SNP_ID_131878981 m1A Human chr3 + 46976715 46976715 46976715 CGCAACGCCTCTTCCTCTAGCCGGCCCACACCAGCCGTAGTTGCCTCCATCTTGCCCGCGTACGC CGCAACGCCTCTTCCTCTAGCCGGCCCACACCCGCCGTAGTTGCCTCCATCTTGCCCGCGTACGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:46976517..46976750 26863196 MeRIP-seq:(Medium) rs948405833 Functional Loss SNV dbSNP153 33..33 33 - - - 87007 RMVar_ID_87007 Human_SNP_ID_131881304 m1A Human chr3 - 46986421 46986421 46986421 CACCTCTCCCCCTCTGTGGTTCACATCCTCCTATCCAGGCCTTTTCCCACCCTATGCCCCACTGC CACCTCTCCCCCTCTGTGGTTCACATCCTCCTGTCCAGGCCTTTTCCCACCCTATGCCCCACTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46986416..46986524 26863196 MeRIP-seq:(Medium) rs1304646868 Functional Loss SNV dbSNP153 33..33 33 - - - 87008 RMVar_ID_87008 Human_SNP_ID_131882750 m1A Human chr3 + 46991534 46991534 46991534 GTGCCACTGGCTCTAGAGGCACTGGTAGGTGCAGTCCATGTCTTGCATGCCAGCCGCGCACCTCC GTGCCACTGGCTCTAGAGGCACTGGTAGGTGCGGTCCATGTCTTGCATGCCAGCCGCGCACCTCC A G NBEAL2 Ensembl:ENSG00000160796 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:46991484..46991594 32194978 MeRIP-seq:(Medium) rs751816975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1627507,Human_RBP_ID_22281377,Human_RBP_ID_27053423 Human_miRNA_ID_2480407,Human_miRNA_ID_2951296 RMVar_hsa_circ_51411,RMVar_hsa_circ_217473,RMVar_hsa_circ_81823,RMVar_hsa_circ_118182,RMVar_hsa_circ_338737,RMVar_hsa_circ_217474,RMVar_hsa_circ_100952,RMVar_hsa_circ_217476 87009 RMVar_ID_87009 Human_SNP_ID_131885647 m1A Human chr3 + 47000054 47000054 47000054 AGTCACCTACCTCCCCCAAGCCAGCCCCACCCAAGCCACCCACTGAGTCACCTGCTGAGCCTTCA AGTCACCTACCTCCCCCAAGCCAGCCCCACCCCAGCCACCCACTGAGTCACCTGCTGAGCCTTCA A C NBEAL2 Ensembl:ENSG00000160796 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47000003..47000145 26863196 MeRIP-seq:(Medium) rs1344750380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17089010 RMVar_hsa_circ_123959,RMVar_hsa_circ_217480,RMVar_hsa_circ_89650,RMVar_hsa_circ_217482 87010 RMVar_ID_87010 Human_SNP_ID_131916245 m1A Human chr3 - 47120343 47120343 47120343 CTTCAGGACAGAAAGAAAGTTAGAGTGGAGGTAGAGCAGGGAGAGACATCAGTGCCCCCAGGTTC CTTCAGGACAGAAAGAAAGTTAGAGTGGAGGTGGAGCAGGGAGAGACATCAGTGCCCCCAGGTTC T C SETD2 Ensembl:ENSG00000181555 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47120292..47120400 26863196 MeRIP-seq:(Medium) rs746006058 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_784174,Human_RBP_ID_836431,Human_RBP_ID_5530347,Human_RBP_ID_7200225,Human_RBP_ID_8872445,Human_RBP_ID_14840319,Human_RBP_ID_17660859,Human_RBP_ID_19029064,Human_RBP_ID_22093009,Human_RBP_ID_22363113,Human_RBP_ID_23026497,Human_RBP_ID_24004926,Human_RBP_ID_26348029,Human_RBP_ID_27822184 RMVar_hsa_circ_117573,RMVar_hsa_circ_108279,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_86365,RMVar_hsa_circ_127672,RMVar_hsa_circ_217522,RMVar_hsa_circ_120152,RMVar_hsa_circ_217531,RMVar_hsa_circ_378001,RMVar_hsa_circ_217534,RMVar_hsa_circ_217533,RMVar_hsa_circ_337046,RMVar_hsa_circ_119859,RMVar_hsa_circ_80479,RMVar_hsa_circ_99340,RMVar_hsa_circ_217547,RMVar_hsa_circ_217548,RMVar_hsa_circ_217546,RMVar_hsa_circ_290604,RMVar_hsa_circ_217549,RMVar_hsa_circ_217550,RMVar_hsa_circ_217552,RMVar_hsa_circ_347111,RMVar_hsa_circ_217553 87011 RMVar_ID_87011 Human_SNP_ID_131927141 m1A Human chr3 + 47163929 47163905 47163929 GAGGCGGCTGCGGCTGCAGCTGCTTCATCGGGAGCGGCTGGAGACGGCGACGCGAGCCCCCTCCC GAGGCGGCT________________________GCGGCTGGAGACGGCGACGCGAGCCCCCTCCC TGCGGCTGCAGCTGCTTCATCGGGA T lnc-KLHL18-7 RNACentral:URS00008BAC0D lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47163881..47164085 26863196 MeRIP-seq:(Medium) rs746501547 Functional Loss DEL dbSNP153 10..33 33 - - - 87012 RMVar_ID_87012 Human_SNP_ID_131927148 m1A Human chr3 - 47163924 47163924 47163924 GGGGCTCGCGTCGCCGTCTCCAGCCGCTCCCGATGAAGCAGCTGCAGCCGCAGCCGCCTCCGAAG GGGGCTCGCGTCGCCGTCTCCAGCCGCTCCCGTTGAAGCAGCTGCAGCCGCAGCCGCCTCCGAAG T A SETD2 Ensembl:ENSG00000181555 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47163876..47164080 26863196 MeRIP-seq:(Medium) rs1003848255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757157,Human_RBP_ID_9333702,Human_RBP_ID_25738734 Human_Splice_Rec_421879 Human_miRNA_ID_2011644,Human_miRNA_ID_2758004 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 87013 RMVar_ID_87013 Human_SNP_ID_131955820 m1A Human chr3 - 47282718 47282718 47282718 CTTCGCATGTGCATCCGCCGAAGTCTTTCTAGATCAATCGGCCCCATCTCTCGTCTTCCCGATTC CTTCGCATGTGCATCCGCCGAAGTCTTTCTAGGTCAATCGGCCCCATCTCTCGTCTTCCCGATTC T C KIF9 Ensembl:ENSG00000088727 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:47282669..47282803;chr3:47282669..47282798 26863196 MeRIP-seq:(Medium) rs903793534 Functional Loss SNV dbSNP153 33..33 33 - - - 87014 RMVar_ID_87014 Human_SNP_ID_131955955 m1A Human chr3 - 47283011 47283011 47283011 GCCGTAGCCGCGACTAGGCAACTCAGACACGGAGAAGTGCACCAGATCCTCCAGCTCCTCCGCGC GCCGTAGCCGCGACTAGGCAACTCAGACACGGTGAAGTGCACCAGATCCTCCAGCTCCTCCGCGC T A KIF9 Ensembl:ENSG00000088727 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:47282960..47283065 26863196 MeRIP-seq:(Medium) rs746645415 Functional Loss SNV dbSNP153 33..33 33 - - - 87015 RMVar_ID_87015 Human_SNP_ID_131979100 m1A Human chr3 - 47381075 47381075 47381075 ACGGCCTCCATGGCGGCTGGCACCCGCCGGCCACCCGGCCACTCCCGTAGCTGCTGCAGCTGCTG ACGGCCTCCATGGCGGCTGGCACCCGCCGGCCCCCCGGCCACTCCCGTAGCTGCTGCAGCTGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47381032..47381139 26863196 MeRIP-seq:(Medium) rs764168368 Functional Loss SNV dbSNP153 33..33 33 - - - 87016 RMVar_ID_87016 Human_SNP_ID_131979139 m1A Human chr3 - 47381161 47381161 47381161 AAGGCAAGCTCACCTTCTTCACAGCTGGCTGGAAGTGAAAGTCACCGGCCTCCTTCAGGTCCAGC AAGGCAAGCTCACCTTCTTCACAGCTGGCTGGTAGTGAAAGTCACCGGCCTCCTTCAGGTCCAGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47381110..47396272 32194978 MeRIP-seq:(Medium) rs745537981 Functional Loss SNV dbSNP153 33..33 33 - - - 87017 RMVar_ID_87017 Human_SNP_ID_131979175 m1A Human chr3 - 47381222 47381222 47381222 GCAGGGGGGCGTCACGCGCTTGCAGACGACGGAGATACGCGGCGGATAGGGGGGAAGATGGAAGG GCAGGGGGGCGTCACGCGCTTGCAGACGACGGCGATACGCGGCGGATAGGGGGGAAGATGGAAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47381211..47381468 26863196 MeRIP-seq:(Medium) rs367949839 Functional Loss SNV dbSNP153 33..33 33 - - - 87018 RMVar_ID_87018 Human_SNP_ID_131979249 m1A Human chr3 - 47381471 47381471 47381471 AGGGGCGGGGCAGAACTGGGTCCGAGCGTCAGAAGGAGGAAGTGTGCTGCCTCAGTGGGAACAGC AGGGGCGGGGCAGAACTGGGTCCGAGCGTCAGGAGGAGGAAGTGTGCTGCCTCAGTGGGAACAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47381284..47381525 26863196 MeRIP-seq:(Medium) rs1476514792 Functional Loss SNV dbSNP153 33..33 33 - - - 87019 RMVar_ID_87019 Human_SNP_ID_131984852 m1A Human chr3 - 47405792 47405792 47405792 TGTTCCACTACTGCCCCTCTCCTCACCTCCTCAGACACCCGCTTGTCCATGGCCCCCAGCATGGA TGTTCCACTACTGCCCCTCTCCTCACCTCCTCGGACACCCGCTTGTCCATGGCCCCCAGCATGGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47405752..47407139 32194978 MeRIP-seq:(Medium) rs1435347247 Functional Loss SNV dbSNP153 33..33 33 - - - 87020 RMVar_ID_87020 Human_SNP_ID_131986345 m1A Human chr3 - 47409975 47409948 47409975 CCACTGCCTCACTCTCCTCCCTGCGGGGCAGCAGCGGCTTTGGGGCTGTGGGCCGTGGCGGCGGC CCACTGCCTCACTCTCCTCCCTGCGGGGCAGC___________________________GGCGGC CGCCACGGCCCACAGCCCCAAAGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47409831..47410251 26863196 MeRIP-seq:(Medium) rs1250723253 Functional Loss DEL dbSNP153 33..59 33 - - - 87021 RMVar_ID_87021 Human_SNP_ID_131986425 m1A Human chr3 - 47410056 47410056 47410056 CCAGGAAGGTGTCAGGCAGTCGTGGGCCAGCCACCATGTCAGGGGGGAGGCTGCGCAGCTCCTCA CCAGGAAGGTGTCAGGCAGTCGTGGGCCAGCCGCCATGTCAGGGGGGAGGCTGCGCAGCTCCTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:47410008..47410132 26863196 MeRIP-seq:(Medium) rs563506036 Functional Loss SNV dbSNP153 33..33 33 - - - 87022 RMVar_ID_87022 Human_SNP_ID_131986430 m1A Human chr3 - 47410071 47410071 47410071 GCGGGGTGGCACTTCCCAGGAAGGTGTCAGGCAGTCGTGGGCCAGCCACCATGTCAGGGGGGAGG GCGGGGTGGCACTTCCCAGGAAGGTGTCAGGCGGTCGTGGGCCAGCCACCATGTCAGGGGGGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47409938..47410469 26863196 MeRIP-seq:(Medium) rs1221216447 Functional Loss SNV dbSNP153 33..33 33 - - - 87023 RMVar_ID_87023 Human_SNP_ID_131986591 m1A Human chr3 - 47410393 47410390 47410393 GCCATGGCCAACTCGGGGCCTGAGAATTGAGGAGGTGGGGCCGAGGGGAGACCTGCAACTGGTGG GCCATGGCCAACTCGGGGCCTGAGAATTGAGG___TGGGGCCGAGGGGAGACCTGCAACTGGTGG ACCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47410344..47410475 26863196 MeRIP-seq:(Medium) rs1248669022 Functional Loss DEL dbSNP153 33..35 33 - - - 87024 RMVar_ID_87024 Human_SNP_ID_131986720 m1A Human chr3 + 47410600 47410595 47410600 TACCCTGCAGGGGCTAAGCAACCCATCCCGGCACAGCACCACTTCTCTTCTGGGATCCCCGCAGG TACCCTGCAGGGGCTAAGCAACCCATCC_____CAGCACCACTTCTCTTCTGGGATCCCCGCAGG CCGGCA C PTPN23 Ensembl:ENSG00000076201 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47410551..47410625 26863196 MeRIP-seq:(Medium) rs1314416228 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_4743622 87025 RMVar_ID_87025 Human_SNP_ID_131986728 m1A Human chr3 - 47410623 47410623 47410623 GCCCAATCCTTGGGGCTGGAAAACCTGCGGGGATCCCAGAAGAGAAGTGGTGCTGTGCCGGGATG GCCCAATCCTTGGGGCTGGAAAACCTGCGGGGGTCCCAGAAGAGAAGTGGTGCTGTGCCGGGATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:47410577..47410678 26863196 MeRIP-seq:(Medium) rs1183621421 Functional Loss SNV dbSNP153 33..33 33 - - - 87026 RMVar_ID_87026 Human_SNP_ID_131986757 m1A Human chr3 - 47410675 47410663 47410675 TGAGGCCCAAACGCTTGTGAAGGATGGGGCTGAGGATGGGGCTGGGGCTGGGGCCCAATCCTTGG TGAGGCCCAAACGCTTGTGAAGGATGGGGCTG____________GGGCTGGGGCCCAATCCTTGG CCAGCCCCATCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:47410627..47410775 26863196 MeRIP-seq:(Medium) rs760022693 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_5506423 87027 RMVar_ID_87027 Human_SNP_ID_131986769 m1A Human chr3 - 47410675 47410671 47410675 TGAGGCCCAAACGCTTGTGAAGGATGGGGCTGAGGATGGGGCTGGGGCTGGGGCCCAATCCTTGG TGAGGCCCAAACGCTTGTGAAGGATGGGGCTG____TGGGGCTGGGGCTGGGGCCCAATCCTTGG ATCCT A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:47410627..47410775 26863196 MeRIP-seq:(Medium) rs1481165461 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5506423 87028 RMVar_ID_87028 Human_SNP_ID_131986772 m1A Human chr3 - 47410675 47410674 47410675 TGAGGCCCAAACGCTTGTGAAGGATGGGGCTGAGGATGGGGCTGGGGCTGGGGCCCAATCCTTGG TGAGGCCCAAACGCTTGTGAAGGATGGGGCTG_GGATGGGGCTGGGGCTGGGGCCCAATCCTTGG CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:47410627..47410775 26863196 MeRIP-seq:(Medium) rs1559528548 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5506423 87029 RMVar_ID_87029 Human_SNP_ID_131986773 m1A Human chr3 - 47410675 47410675 47410675 TGAGGCCCAAACGCTTGTGAAGGATGGGGCTGAGGATGGGGCTGGGGCTGGGGCCCAATCCTTGG TGAGGCCCAAACGCTTGTGAAGGATGGGGCTGGGGATGGGGCTGGGGCTGGGGCCCAATCCTTGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:47410627..47410775 26863196 MeRIP-seq:(Medium) rs546578935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5506423 87030 RMVar_ID_87030 Human_SNP_ID_131986775 m1A Human chr3 + 47410677 47410677 47410677 AAGGATTGGGCCCCAGCCCCAGCCCCATCCTCAGCCCCATCCTTCACAAGCGTTTGGGCCTCAGC AAGGATTGGGCCCCAGCCCCAGCCCCATCCTCGGCCCCATCCTTCACAAGCGTTTGGGCCTCAGC A G PTPN23 Ensembl:ENSG00000076201 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:47410626..47411054 26863196 MeRIP-seq:(Medium) rs1032732779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5133205,Human_RBP_ID_17088560,Human_RBP_ID_17404569,Human_RBP_ID_18954307 87031 RMVar_ID_87031 Human_SNP_ID_131986802 m1A Human chr3 - 47410738 47410737 47410738 AGTCCTGGGGCCTGGGGTGGGAAGAGATGTGGATGCTGGAGTGGAAGGGGCTGCTGTGGGGGCTG AGTCCTGGGGCCTGGGGTGGGAAGAGATGTGG_TGCTGGAGTGGAAGGGGCTGCTGTGGGGGCTG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47410688..47411093 26863196 MeRIP-seq:(Medium) rs867075741 Functional Loss DEL dbSNP153 33..33 33 - - - 87032 RMVar_ID_87032 Human_SNP_ID_131986905 m1A Human chr3 + 47410942 47410942 47410942 AGCCCTGGGCCCCCTCAGCCTCCCCATCCCCCACTGGCATATGGTCCTGCCCCTTCTACCAGACC AGCCCTGGGCCCCCTCAGCCTCCCCATCCCCCCCTGGCATATGGTCCTGCCCCTTCTACCAGACC A C PTPN23 Ensembl:ENSG00000076201 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:47410858..47411000 26863196 MeRIP-seq:(Medium) rs1308366492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785130,Human_RBP_ID_1069143,Human_RBP_ID_3721262,Human_RBP_ID_5133208,Human_RBP_ID_17088564,Human_RBP_ID_17661366,Human_RBP_ID_18953488,Human_RBP_ID_20970705 87033 RMVar_ID_87033 Human_SNP_ID_131987911 m1A Human chr3 - 47413013 47413013 47413013 CCAGGGAGAAGGCCTCTGGGGTCAAGGAGGCCAGCAATTCCAGGGAGGAGGAGGGGGGCCCCGAG CCAGGGAGAAGGCCTCTGGGGTCAAGGAGGCCCGCAATTCCAGGGAGGAGGAGGGGGGCCCCGAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47412965..47413240 26863196 MeRIP-seq:(Medium) rs1390602510 Functional Loss SNV dbSNP153 33..33 33 - - - 87034 RMVar_ID_87034 Human_SNP_ID_131988277 m1A Human chr3 + 47413902 47413900 47413902 AGCACAGAGGGCACATACACCAGGCTGAGCTCACTGCCAAAGTTGCAGACAATGGCAGCGTTGTC AGCACAGAGGGCACATACACCAGGCTGAGCT__CTGCCAAAGTTGCAGACAATGGCAGCGTTGTC TCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47413851..47413925 32194978 MeRIP-seq:(Medium) rs1393786688 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1205575 87035 RMVar_ID_87035 Human_SNP_ID_131988295 m1A Human chr3 - 47413948 47413948 47413948 GGGGAAGAACAGTGAGGCCCAGCCTGCCCGCCAGATCCTGGTGCTGGACAACGCTGCCATTGTCT GGGGAAGAACAGTGAGGCCCAGCCTGCCCGCCTGATCCTGGTGCTGGACAACGCTGCCATTGTCT T A SCAP Ensembl:ENSG00000114650 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:47413901..47414000 32194978 MeRIP-seq:(Medium) rs1351671116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602987,Human_RBP_ID_5120697,Human_RBP_ID_5150328,Human_RBP_ID_5325533,Human_RBP_ID_9141155,Human_RBP_ID_18169282,Human_RBP_ID_18809262 Human_miRNA_ID_740501,Human_miRNA_ID_744514,Human_miRNA_ID_748515,Human_miRNA_ID_972376,Human_miRNA_ID_2299498,Human_miRNA_ID_2302771,Human_miRNA_ID_2306033 RMVar_hsa_circ_217573,RMVar_hsa_circ_125680 87036 RMVar_ID_87036 Human_SNP_ID_131988662 m1A Human chr3 - 47414942 47414942 47414942 TTCCCCTGCCTCTCCAGTGTACAGCAGCAGCGACACAGTGGCCTGTCACCTGACCCACACAGTGC TTCCCCTGCCTCTCCAGTGTACAGCAGCAGCGGCACAGTGGCCTGTCACCTGACCCACACAGTGC T C SCAP Ensembl:ENSG00000114650 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47414876..47414975 32194978 MeRIP-seq:(Medium) rs1272984976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19011812,Human_RBP_ID_22677763,Human_RBP_ID_24005198 Human_Splice_Rec_422442,Human_Splice_Rec_422482,Human_Splice_Rec_422516,Human_Splice_Rec_422554,Human_Splice_Rec_422580,Human_Splice_Rec_422626 RMVar_hsa_circ_127864,RMVar_hsa_circ_102906,RMVar_hsa_circ_106036,RMVar_hsa_circ_217573,RMVar_hsa_circ_125680,RMVar_hsa_circ_104489,RMVar_hsa_circ_217575,RMVar_hsa_circ_38384,RMVar_hsa_circ_217576,RMVar_hsa_circ_217574,RMVar_hsa_circ_265995,RMVar_hsa_circ_217578,RMVar_hsa_circ_81144,RMVar_hsa_circ_110377,RMVar_hsa_circ_217579,RMVar_hsa_circ_217580,RMVar_hsa_circ_109169,RMVar_hsa_circ_268127,RMVar_hsa_circ_269036,RMVar_hsa_circ_217581 87037 RMVar_ID_87037 Human_SNP_ID_131988663 m1A Human chr3 - 47414942 47414942 47414942 TTCCCCTGCCTCTCCAGTGTACAGCAGCAGCGACACAGTGGCCTGTCACCTGACCCACACAGTGC TTCCCCTGCCTCTCCAGTGTACAGCAGCAGCGCCACAGTGGCCTGTCACCTGACCCACACAGTGC T G SCAP Ensembl:ENSG00000114650 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47414876..47414975 32194978 MeRIP-seq:(Medium) rs1272984976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19011812,Human_RBP_ID_22677763,Human_RBP_ID_24005198 Human_Splice_Rec_422442,Human_Splice_Rec_422482,Human_Splice_Rec_422516,Human_Splice_Rec_422554,Human_Splice_Rec_422580,Human_Splice_Rec_422626 RMVar_hsa_circ_127864,RMVar_hsa_circ_102906,RMVar_hsa_circ_106036,RMVar_hsa_circ_217573,RMVar_hsa_circ_125680,RMVar_hsa_circ_104489,RMVar_hsa_circ_217575,RMVar_hsa_circ_38384,RMVar_hsa_circ_217576,RMVar_hsa_circ_217574,RMVar_hsa_circ_265995,RMVar_hsa_circ_217578,RMVar_hsa_circ_81144,RMVar_hsa_circ_110377,RMVar_hsa_circ_217579,RMVar_hsa_circ_217580,RMVar_hsa_circ_109169,RMVar_hsa_circ_268127,RMVar_hsa_circ_269036,RMVar_hsa_circ_217581 87038 RMVar_ID_87038 Human_SNP_ID_131996372 m1A Human chr3 + 47443026 47443026 47443026 CCTCAGCCGAAGTCACCTTGCTGCCATCCCGGAAAGTGACCATGGATCACCCTGGCACACACTTG CCTCAGCCGAAGTCACCTTGCTGCCATCCCGGGAAGTGACCATGGATCACCCTGGCACACACTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47442976..47443137 26863196 MeRIP-seq:(Medium) rs1278092216 Functional Loss SNV dbSNP153 33..33 33 - - - 87039 RMVar_ID_87039 Human_SNP_ID_132004283 m1A Human chr3 + 47475845 47475845 47475845 CCTCCCAAGCTGCGGCGGCGGCGGCGGCGGCGACGGGGGCGGCAGCAGGGGCGGAGCGCGGCGTG CCTCCCAAGCTGCGGCGGCGGCGGCGGCGGCGGCGGGGGCGGCAGCAGGGGCGGAGCGCGGCGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:47475748..47475988;chr3:47475735..47476006;chr3:47475742..47475976 26863196 MeRIP-seq:(Medium) rs1240635211 Functional Loss SNV dbSNP153 33..33 33 - - - 87040 RMVar_ID_87040 Human_SNP_ID_132011033 m1A Human chr3 - 47501741 47501741 47501741 TCGGTGGACGTACCCGGTGCTGTTGGTGGACGACCTCAGTGTGCTCCTGAGCCTGGGCATGGGGG TCGGTGGACGTACCCGGTGCTGTTGGTGGACGGCCTCAGTGTGCTCCTGAGCCTGGGCATGGGGG T C ELP6 Ensembl:ENSG00000163832 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47501691..47501840 32194978 MeRIP-seq:(Medium) rs752000466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603045,Human_RBP_ID_5325215,Human_RBP_ID_18006588 Human_Splice_Rec_422685,Human_Splice_Rec_422695,Human_Splice_Rec_422705,Human_Splice_Rec_422717,Human_Splice_Rec_422729,Human_Splice_Rec_422739,Human_Splice_Rec_422751 Human_miRNA_ID_678280 RMVar_hsa_circ_97615,RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_288489,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_346690,RMVar_hsa_circ_217621,RMVar_hsa_circ_319812,RMVar_hsa_circ_217625,RMVar_hsa_circ_217626,RMVar_hsa_circ_217624,RMVar_hsa_circ_316161,RMVar_hsa_circ_217627,RMVar_hsa_circ_217628 87041 RMVar_ID_87041 Human_SNP_ID_132013856 m1A Human chr3 - 47512832 47512832 47512832 AGGAGAGGGGAGTTCGTTTCGCCGCCGTCTTCATGGGCGAGCTTCCTAACCGCCACCTCGCCCCG AGGAGAGGGGAGTTCGTTTCGCCGCCGTCTTCTTGGGCGAGCTTCCTAACCGCCACCTCGCCCCG T A ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47512830..47512918 26863196 MeRIP-seq:(Medium) rs115562604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 87042 RMVar_ID_87042 Human_SNP_ID_132013857 m1A Human chr3 - 47512832 47512832 47512832 AGGAGAGGGGAGTTCGTTTCGCCGCCGTCTTCATGGGCGAGCTTCCTAACCGCCACCTCGCCCCG AGGAGAGGGGAGTTCGTTTCGCCGCCGTCTTCGTGGGCGAGCTTCCTAACCGCCACCTCGCCCCG T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47512830..47512918 26863196 MeRIP-seq:(Medium) rs115562604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 87043 RMVar_ID_87043 Human_SNP_ID_132013863 m1A Human chr3 - 47512861 47512861 47512861 CTCAGAGGAGACTGCAGAATAGGCCCGAGAGGAGAGGGGAGTTCGTTTCGCCGCCGTCTTCATGG CTCAGAGGAGACTGCAGAATAGGCCCGAGAGGTGAGGGGAGTTCGTTTCGCCGCCGTCTTCATGG T A ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:47512857..47512975 26863196 MeRIP-seq:(Medium) rs746274795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14845064 RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 87044 RMVar_ID_87044 Human_SNP_ID_132013959 m1A Human chr3 + 47513235 47513235 47513235 ACTTGTCTCGAACTCTTGACCTTAGATGATGCACCCGCCTCGGCCTCCCAAACTGCTGGGATTAC ACTTGTCTCGAACTCTTGACCTTAGATGATGCCCCCGCCTCGGCCTCCCAAACTGCTGGGATTAC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:47513181..47513290 26863410 MeRIP-seq:(Medium) rs936870409 Functional Loss SNV dbSNP153 33..33 33 - - - 87045 RMVar_ID_87045 Human_SNP_ID_132013964 m1A Human chr3 + 47513253 47513253 47513253 ACCTTAGATGATGCACCCGCCTCGGCCTCCCAAACTGCTGGGATTACAGGGGTGAGCCACCGCGC ACCTTAGATGATGCACCCGCCTCGGCCTCCCAGACTGCTGGGATTACAGGGGTGAGCCACCGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:47513100..47513314;chr3:47513006..47513347 26863196 MeRIP-seq:(Medium) rs1056237034 Functional Loss SNV dbSNP153 33..33 33 - - - 87046 RMVar_ID_87046 Human_SNP_ID_132029735 m1A Human chr3 - 47577089 47577089 47577089 TGCCCACTGGGAAGCCTGGTCTGGGGCCCGGGACAGGCCAGCCCACCAGTCGGTGGCATGCTGTC TGCCCACTGGGAAGCCTGGTCTGGGGCCCGGGGCAGGCCAGCCCACCAGTCGGTGGCATGCTGTC T C CSPG5 Ensembl:ENSG00000114646 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47577044..47577133 26863196 MeRIP-seq:(Medium) rs773713041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1313057 Human_miRNA_ID_2224923,Human_miRNA_ID_2872662,Human_miRNA_ID_2980629 RMVar_hsa_circ_103589,RMVar_hsa_circ_217635 87047 RMVar_ID_87047 Human_SNP_ID_132030010 m1A Human chr3 - 47577856 47577856 47577856 GAAGGGCAGCCCGGCGTGGGAGCCGCCTGCCAACGACACGCGGGAAGAAGCCGGCCCACCAGCGG GAAGGGCAGCCCGGCGTGGGAGCCGCCTGCCAGCGACACGCGGGAAGAAGCCGGCCCACCAGCGG T C CSPG5 Ensembl:ENSG00000114646 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47577501..47577951 26863196 MeRIP-seq:(Medium) rs1178981752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18006611 Human_Splice_Rec_422796,Human_Splice_Rec_422810,Human_Splice_Rec_422818,Human_Splice_Rec_422824 RMVar_hsa_circ_103589,RMVar_hsa_circ_217635,RMVar_hsa_circ_217638 87048 RMVar_ID_87048 Human_SNP_ID_132030357 m1A Human chr3 + 47578708 47578708 47578708 GCCCCCGGCTCGCCCCATGGCGCGGCGCCCCGACCGCTGTCCGCGGTCCGCCCGGCTGGCTGCGC GCCCCCGGCTCGCCCCATGGCGCGGCGCCCCGCCCGCTGTCCGCGGTCCGCCCGGCTGGCTGCGC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:47578604..47578736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 87049 RMVar_ID_87049 Human_SNP_ID_132030358 m1A Human chr3 + 47578708 47578708 47578708 GCCCCCGGCTCGCCCCATGGCGCGGCGCCCCGACCGCTGTCCGCGGTCCGCCCGGCTGGCTGCGC GCCCCCGGCTCGCCCCATGGCGCGGCGCCCCGTCCGCTGTCCGCGGTCCGCCCGGCTGGCTGCGC A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:47578604..47578736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 87050 RMVar_ID_87050 Human_SNP_ID_132032649 m1A Human chr3 + 47588299 47588299 47588299 GGTGGTGGTGGCGGTGGCTGCTGCTGTGGTGGAGGGGGATCTGCAAACATATCCAAGAGTAACTC GGTGGTGGTGGCGGTGGCTGCTGCTGTGGTGGGGGGGGATCTGCAAACATATCCAAGAGTAACTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47588251..47588325 26863196 MeRIP-seq:(Medium) rs368443987 Functional Loss SNV dbSNP153 33..33 33 - - - 87051 RMVar_ID_87051 Human_SNP_ID_132032650 m1A Human chr3 + 47588299 47588299 47588299 GGTGGTGGTGGCGGTGGCTGCTGCTGTGGTGGAGGGGGATCTGCAAACATATCCAAGAGTAACTC GGTGGTGGTGGCGGTGGCTGCTGCTGTGGTGGTGGGGGATCTGCAAACATATCCAAGAGTAACTC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47588251..47588325 26863196 MeRIP-seq:(Medium) rs368443987 Functional Loss SNV dbSNP153 33..33 33 - - - 87052 RMVar_ID_87052 Human_SNP_ID_132033232 m1A Human chr3 - 47590686 47590686 47590686 CCAATGCCAGGAAACATCTTAGGACCCCGGGTACCCCTGACAGCACCTAACGGCATGTGTAAGTA CCAATGCCAGGAAACATCTTAGGACCCCGGGTGCCCCTGACAGCACCTAACGGCATGTGTAAGTA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47590676..47590700 26863196 MeRIP-seq:(Medium) rs762541539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1963747,Human_RBP_ID_7201113,Human_RBP_ID_8573676,Human_RBP_ID_8872584,Human_RBP_ID_14845867 Human_Splice_Rec_422877,Human_Splice_Rec_422929 RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_266832,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_269577,RMVar_hsa_circ_38335,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641 87053 RMVar_ID_87053 Human_SNP_ID_132050467 m1A Human chr3 - 47661389 47661389 47661389 GGAATTGGTTGAAGCTCATGTCAAGAAAGTACAAGAAGCAGCACGAGCCTCTGGGAAAGTGGATC GGAATTGGTTGAAGCTCATGTCAAGAAAGTACGAGAAGCAGCACGAGCCTCTGGGAAAGTGGATC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47661214..47661450 26863196 MeRIP-seq:(Medium) rs768188371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68972,Human_RBP_ID_1627734,Human_RBP_ID_1963806,Human_RBP_ID_2787281,Human_RBP_ID_4744032,Human_RBP_ID_9393519,Human_RBP_ID_22281748,Human_RBP_ID_22823685,Human_RBP_ID_26823790 Human_Splice_Rec_422864,Human_Splice_Rec_422865,Human_Splice_Rec_422916,Human_Splice_Rec_422917 RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_41465,RMVar_hsa_circ_217644,RMVar_hsa_circ_217646,RMVar_hsa_circ_217647,RMVar_hsa_circ_217645,RMVar_hsa_circ_302167,RMVar_hsa_circ_323863,RMVar_hsa_circ_217643,RMVar_hsa_circ_355847,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_15213,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_217663,RMVar_hsa_circ_298792,RMVar_hsa_circ_342559,RMVar_hsa_circ_375152,RMVar_hsa_circ_308076,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217669,RMVar_hsa_circ_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665,RMVar_hsa_circ_112057,RMVar_hsa_circ_294805,RMVar_hsa_circ_318682,RMVar_hsa_circ_367020,RMVar_hsa_circ_217668,RMVar_hsa_circ_343286,RMVar_hsa_circ_317580,RMVar_hsa_circ_274119,RMVar_hsa_circ_276369,RMVar_hsa_circ_272889,RMVar_hsa_circ_217672,RMVar_hsa_circ_37658,RMVar_hsa_circ_64960,RMVar_hsa_circ_217674,RMVar_hsa_circ_217675,RMVar_hsa_circ_217673,RMVar_hsa_circ_217670,RMVar_hsa_circ_217671 87054 RMVar_ID_87054 Human_SNP_ID_132050473 m1A Human chr3 - 47661399 47661399 47661399 AGGTACCACTGGAATTGGTTGAAGCTCATGTCAAGAAAGTACAAGAAGCAGCACGAGCCTCTGGG AGGTACCACTGGAATTGGTTGAAGCTCATGTCGAGAAAGTACAAGAAGCAGCACGAGCCTCTGGG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47661276..47661400 32194978 MeRIP-seq:(Medium) rs1287968314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68972,Human_RBP_ID_1627734,Human_RBP_ID_1963806,Human_RBP_ID_2787281,Human_RBP_ID_9393519,Human_RBP_ID_14847815,Human_RBP_ID_22281749,Human_RBP_ID_24005531 Human_Splice_Rec_422864,Human_Splice_Rec_422916 RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_41465,RMVar_hsa_circ_217644,RMVar_hsa_circ_217646,RMVar_hsa_circ_217647,RMVar_hsa_circ_217645,RMVar_hsa_circ_302167,RMVar_hsa_circ_323863,RMVar_hsa_circ_217643,RMVar_hsa_circ_355847,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_15213,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_217663,RMVar_hsa_circ_298792,RMVar_hsa_circ_342559,RMVar_hsa_circ_375152,RMVar_hsa_circ_308076,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217669,RMVar_hsa_circ_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665,RMVar_hsa_circ_112057,RMVar_hsa_circ_294805,RMVar_hsa_circ_318682,RMVar_hsa_circ_367020,RMVar_hsa_circ_217668,RMVar_hsa_circ_343286,RMVar_hsa_circ_317580,RMVar_hsa_circ_274119,RMVar_hsa_circ_276369,RMVar_hsa_circ_272889,RMVar_hsa_circ_217672,RMVar_hsa_circ_37658,RMVar_hsa_circ_64960,RMVar_hsa_circ_217674,RMVar_hsa_circ_217675,RMVar_hsa_circ_217673,RMVar_hsa_circ_217670,RMVar_hsa_circ_217671 87055 RMVar_ID_87055 Human_SNP_ID_132050687 m1A Human chr3 - 47662293 47662293 47662293 TTCCCTAAACCATCTCCTCAACAGAAAAACTCAGTTTATCCCAATTTAAATATTACCAGCCGTTA TTCCCTAAACCATCTCCTCAACAGAAAAACTCCGTTTATCCCAATTTAAATATTACCAGCCGTTA T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47662286..47662364 26863196 MeRIP-seq:(Medium) rs1441178838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_318875,RMVar_hsa_circ_41465,RMVar_hsa_circ_217644,RMVar_hsa_circ_217646,RMVar_hsa_circ_217647,RMVar_hsa_circ_217645,RMVar_hsa_circ_323863,RMVar_hsa_circ_217643,RMVar_hsa_circ_355847,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_15213,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_358271,RMVar_hsa_circ_71489,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_217663,RMVar_hsa_circ_298792,RMVar_hsa_circ_342559,RMVar_hsa_circ_375152,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217669,RMVar_hsa_circ_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665,RMVar_hsa_circ_112057,RMVar_hsa_circ_294805,RMVar_hsa_circ_318682,RMVar_hsa_circ_367020,RMVar_hsa_circ_217668,RMVar_hsa_circ_343286,RMVar_hsa_circ_317580,RMVar_hsa_circ_274119,RMVar_hsa_circ_276369,RMVar_hsa_circ_272889,RMVar_hsa_circ_217672,RMVar_hsa_circ_64960,RMVar_hsa_circ_217674,RMVar_hsa_circ_217675,RMVar_hsa_circ_217673,RMVar_hsa_circ_217670,RMVar_hsa_circ_217671 87056 RMVar_ID_87056 Human_SNP_ID_132051115 m1A Human chr3 + 47663744 47663744 47663744 GAGTTTCAAGGAAAAGTTCCTTCACAAGACCCACGAGAACCCGGTGGTACCCATAGGTTGCCTGG GAGTTTCAAGGAAAAGTTCCTTCACAAGACCCGCGAGAACCCGGTGGTACCCATAGGTTGCCTGG A G AC130472.1 Ensembl:ENSG00000235695 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1286852520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1835569 87057 RMVar_ID_87057 Human_SNP_ID_132079597 m1A Human chr3 + 47772928 47772928 47772928 CCAGCCAGTGTTTTATTGGTAGGAGCATCCGCATGAACATACTGCAAGATAAAGACAGGCATTCA CCAGCCAGTGTTTTATTGGTAGGAGCATCCGCGTGAACATACTGCAAGATAAAGACAGGCATTCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47772926..47772950 26863196 MeRIP-seq:(Medium) rs546753729 Functional Loss SNV dbSNP153 33..33 33 - - - 87058 RMVar_ID_87058 Human_SNP_ID_132082189 m1A Human chr3 - 47781762 47781762 47781762 GCCGCAGCGGCGGGCGGCGGCGGGCCGGGGACAGCGGTAGGCGCCACGGGCTCGGGGATTGCGGC GCCGCAGCGGCGGGCGGCGGCGGGCCGGGGACGGCGGTAGGCGCCACGGGCTCGGGGATTGCGGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:47781702..47781898 26863410 MeRIP-seq:(Medium) rs1440195403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69008,Human_RBP_ID_247838,Human_RBP_ID_836040,Human_RBP_ID_3963923,Human_RBP_ID_8875451,Human_RBP_ID_9302239,Human_RBP_ID_9394882,Human_RBP_ID_18423962,Human_RBP_ID_18544776,Human_RBP_ID_22533861,Human_RBP_ID_23115859,Human_RBP_ID_26348071 Human_miRNA_ID_2027008,Human_miRNA_ID_2937212 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_122716,RMVar_hsa_circ_217741,RMVar_hsa_circ_99953,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_217764 87059 RMVar_ID_87059 Human_SNP_ID_132082208 m1A Human chr3 - 47781789 47781789 47781789 CTGTGGGGACGACGGGCTGCGACGATGGCCGCAGCGGCGGGCGGCGGCGGGCCGGGGACAGCGGT CTGTGGGGACGACGGGCTGCGACGATGGCCGCGGCGGCGGGCGGCGGCGGGCCGGGGACAGCGGT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr3:47781651..47781925;chr3:47772935..47781852 26863196,26863410 MeRIP-seq:(Medium) rs1226755865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247838,Human_RBP_ID_836040,Human_RBP_ID_938224,Human_RBP_ID_3963923,Human_RBP_ID_8875452,Human_RBP_ID_9302239,Human_RBP_ID_9354382,Human_RBP_ID_9394882,Human_RBP_ID_18423962,Human_RBP_ID_22533861,Human_RBP_ID_23115859,Human_RBP_ID_26346855 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_122716,RMVar_hsa_circ_217741,RMVar_hsa_circ_99953,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_217764 87060 RMVar_ID_87060 Human_SNP_ID_132082247 m1A Human chr3 - 47781846 47781846 47781846 CGCGGGGGTGCGCGCGGGAACGACCGGGAAACACCGCGAGGGCCGGGGTGGGCCAGGCTGTGGGG CGCGGGGGTGCGCGCGGGAACGACCGGGAAACGCCGCGAGGGCCGGGGTGGGCCAGGCTGTGGGG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:47781744..47781850 26863410 MeRIP-seq:(Medium) rs1407138374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4744144,Human_RBP_ID_8875452,Human_RBP_ID_9302239,Human_RBP_ID_9354382,Human_RBP_ID_18423962,Human_RBP_ID_23115859 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_122716,RMVar_hsa_circ_217741,RMVar_hsa_circ_99953,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_217764 87061 RMVar_ID_87061 Human_SNP_ID_132082249 m1A Human chr3 - 47781848 47781848 47781848 CGCGCGGGGGTGCGCGCGGGAACGACCGGGAAACACCGCGAGGGCCGGGGTGGGCCAGGCTGTGG CGCGCGGGGGTGCGCGCGGGAACGACCGGGAATCACCGCGAGGGCCGGGGTGGGCCAGGCTGTGG T A SMARCC1 Ensembl:ENSG00000173473 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:47781751..47781852 26863410 MeRIP-seq:(Medium) rs912356132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69009,Human_RBP_ID_8875452,Human_RBP_ID_9302239,Human_RBP_ID_9354382,Human_RBP_ID_18423962,Human_RBP_ID_23115859 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_122716,RMVar_hsa_circ_217741,RMVar_hsa_circ_99953,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_217764 87062 RMVar_ID_87062 Human_SNP_ID_132082250 m1A Human chr3 - 47781848 47781848 47781848 CGCGCGGGGGTGCGCGCGGGAACGACCGGGAAACACCGCGAGGGCCGGGGTGGGCCAGGCTGTGG CGCGCGGGGGTGCGCGCGGGAACGACCGGGAAGCACCGCGAGGGCCGGGGTGGGCCAGGCTGTGG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:47781751..47781852 26863410 MeRIP-seq:(Medium) rs912356132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69009,Human_RBP_ID_8875452,Human_RBP_ID_9302239,Human_RBP_ID_9354382,Human_RBP_ID_18423962,Human_RBP_ID_23115859 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_122716,RMVar_hsa_circ_217741,RMVar_hsa_circ_99953,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_217764 87063 RMVar_ID_87063 Human_SNP_ID_132088162 m1A Human chr3 + 47803199 47803199 47803199 GCTCATGCGCGGTGCACAGAGGCTTGTTTCACATCTGTAACAACAGGTGAATTGGGCTTTTTATT GCTCATGCGCGGTGCACAGAGGCTTGTTTCACCTCTGTAACAACAGGTGAATTGGGCTTTTTATT A C DHX30 Ensembl:ENSG00000132153 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47802972..47803251 26863196 MeRIP-seq:(Medium) rs1285176020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603183 Human_Splice_Rec_422977,Human_Splice_Rec_422983,Human_Splice_Rec_422993,Human_Splice_Rec_423005,Human_Splice_Rec_423015,Human_Splice_Rec_423059,Human_Splice_Rec_423075,Human_Splice_Rec_423117 87064 RMVar_ID_87064 Human_SNP_ID_132088619 m1A Human chr3 - 47805279 47805279 47805279 GCTGAGTCAATACAGTGGAGGCCCCATAGGGAAAGAAAGTTGCTCCAACCATCATTTACTAGCTC GCTGAGTCAATACAGTGGAGGCCCCATAGGGATAGAAAGTTGCTCCAACCATCATTTACTAGCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47805277..47805349 26863196 MeRIP-seq:(Medium) rs1401902681 Functional Loss SNV dbSNP153 33..33 33 - - - 87065 RMVar_ID_87065 Human_SNP_ID_132093579 m1A Human chr3 - 47825114 47825114 47825114 GAGAAGCCGCGCGAGCGACCCTGTCGCCCAGCAGCGCGGGGACCCAGCGGCTGCAGGCGCGGAGA GAGAAGCCGCGCGAGCGACCCTGTCGCCCAGCGGCGCGGGGACCCAGCGGCTGCAGGCGCGGAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47825063..47825184 26863196 MeRIP-seq:(Medium) rs1410832120 Functional Loss SNV dbSNP153 33..33 33 - - - 87066 RMVar_ID_87066 Human_SNP_ID_132094220 m1A Human chr3 - 47827462 47827462 47827462 GCCACCAGCAGAGTTACCTTTTTCTTCGGTCCATTTGTGTGCACGTAGACTAGTTTGTCTTTTGC GCCACCAGCAGAGTTACCTTTTTCTTCGGTCCGTTTGTGTGCACGTAGACTAGTTTGTCTTTTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47827413..47827515 26863196 MeRIP-seq:(Medium) rs1559700926 Functional Loss SNV dbSNP153 33..33 33 - - - 87067 RMVar_ID_87067 Human_SNP_ID_132097954 m1A Human chr3 + 47841085 47841085 47841085 ATCCCGCTCTTTAGGCCGGGAAGAAGAGGAGGACGAGGAGGAAGAGCTAGAAGAAGGGACCATAG ATCCCGCTCTTTAGGCCGGGAAGAAGAGGAGGGCGAGGAGGAAGAGCTAGAAGAAGGGACCATAG A G DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:47841035..47841154 26863196 MeRIP-seq:(Medium) rs1393728346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783289,Human_RBP_ID_933083,Human_RBP_ID_4756429,Human_RBP_ID_5602525,Human_RBP_ID_7202083,Human_RBP_ID_23026502 Human_Splice_Rec_423029,Human_Splice_Rec_423073,Human_Splice_Rec_423087,Human_Splice_Rec_423131,Human_Splice_Rec_423169,Human_Splice_Rec_423205,Human_Splice_Rec_423241 RMVar_hsa_circ_83828,RMVar_hsa_circ_40330,RMVar_hsa_circ_6033,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_12432,RMVar_hsa_circ_88259,RMVar_hsa_circ_277515,RMVar_hsa_circ_217769,RMVar_hsa_circ_374956,RMVar_hsa_circ_100492,RMVar_hsa_circ_217770,RMVar_hsa_circ_217772,RMVar_hsa_circ_217773,RMVar_hsa_circ_217771 87068 RMVar_ID_87068 Human_SNP_ID_132097961 m1A Human chr3 + 47841101 47841101 47841101 CGGGAAGAAGAGGAGGACGAGGAGGAAGAGCTAGAAGAAGGGACCATAGATGTTACCGACTTCTT CGGGAAGAAGAGGAGGACGAGGAGGAAGAGCTGGAAGAAGGGACCATAGATGTTACCGACTTCTT A G DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47841051..47841157 26863196 MeRIP-seq:(Medium) rs1464835988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933083,Human_RBP_ID_7202083,Human_RBP_ID_23026502 Human_Splice_Rec_423029,Human_Splice_Rec_423073,Human_Splice_Rec_423087,Human_Splice_Rec_423131,Human_Splice_Rec_423169,Human_Splice_Rec_423205,Human_Splice_Rec_423241 RMVar_hsa_circ_83828,RMVar_hsa_circ_40330,RMVar_hsa_circ_6033,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_12432,RMVar_hsa_circ_88259,RMVar_hsa_circ_277515,RMVar_hsa_circ_217769,RMVar_hsa_circ_374956,RMVar_hsa_circ_100492,RMVar_hsa_circ_217770,RMVar_hsa_circ_217772,RMVar_hsa_circ_217773,RMVar_hsa_circ_217771 87069 RMVar_ID_87069 Human_SNP_ID_132098183 m1A Human chr3 - 47841900 47841900 47841900 TCCCTGTGCTGCTGAGGCTTGACCTCCATTCCATCACACCTGCTGCTTTTCCTCCCAAGCAGGAG TCCCTGTGCTGCTGAGGCTTGACCTCCATTCCGTCACACCTGCTGCTTTTCCTCCCAAGCAGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47841882..47842006 26863196 MeRIP-seq:(Medium) rs1327864836 Functional Loss SNV dbSNP153 33..33 33 - - - 87070 RMVar_ID_87070 Human_SNP_ID_132099248 m1A Human chr3 + 47846266 47846266 47846266 AAGGACTCAGGGCCTCTGAGTGACCCTATCACAGGCAAGCCCTATGTGCCCCTGTTGGAAGCAGA AAGGACTCAGGGCCTCTGAGTGACCCTATCACGGGCAAGCCCTATGTGCCCCTGTTGGAAGCAGA A G DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47846218..47846366 26863196 MeRIP-seq:(Medium) rs1193223351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603202,Human_RBP_ID_8872641,Human_RBP_ID_18446657,Human_RBP_ID_27054052,Human_RBP_ID_27319021 RMVar_hsa_circ_83828,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_100492,RMVar_hsa_circ_124152,RMVar_hsa_circ_217772,RMVar_hsa_circ_217773,RMVar_hsa_circ_100897,RMVar_hsa_circ_217774,RMVar_hsa_circ_217775 87071 RMVar_ID_87071 Human_SNP_ID_132099411 m1A Human chr3 + 47846817 47846817 47846817 GCTGATCCTGCTCAAGGGCCTGCAGCGGCTCAACCCGGCCCTGCGGCTGGTGCTCATGAGTGCCA GCTGATCCTGCTCAAGGGCCTGCAGCGGCTCACCCCGGCCCTGCGGCTGGTGCTCATGAGTGCCA A C DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47846510..47846850 32194978 MeRIP-seq:(Medium) rs764277096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247303,Human_RBP_ID_8874979,Human_RBP_ID_9302865,Human_RBP_ID_22091656,Human_RBP_ID_24535548 Human_miRNA_ID_1195674,Human_miRNA_ID_2302776,Human_miRNA_ID_2572296 RMVar_hsa_circ_83828,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_100492,RMVar_hsa_circ_124152,RMVar_hsa_circ_217772,RMVar_hsa_circ_217773,RMVar_hsa_circ_100897,RMVar_hsa_circ_217774,RMVar_hsa_circ_217775 87072 RMVar_ID_87072 Human_SNP_ID_132099412 m1A Human chr3 + 47846817 47846817 47846817 GCTGATCCTGCTCAAGGGCCTGCAGCGGCTCAACCCGGCCCTGCGGCTGGTGCTCATGAGTGCCA GCTGATCCTGCTCAAGGGCCTGCAGCGGCTCAGCCCGGCCCTGCGGCTGGTGCTCATGAGTGCCA A G DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47846510..47846850 32194978 MeRIP-seq:(Medium) rs764277096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247303,Human_RBP_ID_8874979,Human_RBP_ID_9302865,Human_RBP_ID_22091656,Human_RBP_ID_24535548 Human_miRNA_ID_1195674,Human_miRNA_ID_2302776,Human_miRNA_ID_2572296 RMVar_hsa_circ_83828,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_100492,RMVar_hsa_circ_124152,RMVar_hsa_circ_217772,RMVar_hsa_circ_217773,RMVar_hsa_circ_100897,RMVar_hsa_circ_217774,RMVar_hsa_circ_217775 87073 RMVar_ID_87073 Human_SNP_ID_132099872 m1A Human chr3 + 47848333 47848333 47848333 TGGTCCCTTTCCAAGTGCCAGAGATCCTGCGCACACCTCTTGAGAACCTGGTGCTGCAAGCGAAA TGGTCCCTTTCCAAGTGCCAGAGATCCTGCGCTCACCTCTTGAGAACCTGGTGCTGCAAGCGAAA A T DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47848179..47848392 26863196 MeRIP-seq:(Medium) rs1441091270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3709503,Human_RBP_ID_5120699,Human_RBP_ID_8872679,Human_RBP_ID_18809531,Human_RBP_ID_19010107 Human_Splice_Rec_423045,Human_Splice_Rec_423103,Human_Splice_Rec_423147,Human_Splice_Rec_423185,Human_Splice_Rec_423221,Human_Splice_Rec_423257,Human_Splice_Rec_423281 Human_miRNA_ID_44119,Human_miRNA_ID_72834,Human_miRNA_ID_206246,Human_miRNA_ID_1490363,Human_miRNA_ID_2299504,Human_miRNA_ID_2302777,Human_miRNA_ID_2306039,Human_miRNA_ID_2780722,Human_miRNA_ID_2786289 RMVar_hsa_circ_15846,RMVar_hsa_circ_124152,RMVar_hsa_circ_100897,RMVar_hsa_circ_217774,RMVar_hsa_circ_115410,RMVar_hsa_circ_121322,RMVar_hsa_circ_217775,RMVar_hsa_circ_217776,RMVar_hsa_circ_217777,RMVar_hsa_circ_86193,RMVar_hsa_circ_217778 87074 RMVar_ID_87074 Human_SNP_ID_132100882 m1A Human chr3 - 47850960 47850960 47850960 GACAGGTTCCAGGTCCTTTCACTCCTTTGGCCAAAGGTTGGGGGTAGGTGGCCCAAGTGGCGTGC GACAGGTTCCAGGTCCTTTCACTCCTTTGGCCTAAGGTTGGGGGTAGGTGGCCCAAGTGGCGTGC T A MAP4 Ensembl:ENSG00000047849 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47850739..47851540 32194978 MeRIP-seq:(Medium) rs182304787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603231,Human_RBP_ID_3721935,Human_RBP_ID_5120528,Human_RBP_ID_8573874 RMVar_hsa_circ_217783,RMVar_hsa_circ_124585 87075 RMVar_ID_87075 Human_SNP_ID_132100889 m1A Human chr3 + 47851002 47851002 47851002 AGTGAAAGGACCTGGAACCTGTCGTCAACCTCAGCATCCTCATGACCCCAGGACAGACGCAGTGG AGTGAAAGGACCTGGAACCTGTCGTCAACCTCCGCATCCTCATGACCCCAGGACAGACGCAGTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47850951..47851210 26863196 MeRIP-seq:(Medium) rs1426375125 Functional Loss SNV dbSNP153 33..33 33 - - - 87076 RMVar_ID_87076 Human_SNP_ID_132100890 m1A Human chr3 + 47851002 47851002 47851002 AGTGAAAGGACCTGGAACCTGTCGTCAACCTCAGCATCCTCATGACCCCAGGACAGACGCAGTGG AGTGAAAGGACCTGGAACCTGTCGTCAACCTCGGCATCCTCATGACCCCAGGACAGACGCAGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47850951..47851210 26863196 MeRIP-seq:(Medium) rs1426375125 Functional Loss SNV dbSNP153 33..33 33 - - - 87077 RMVar_ID_87077 Human_SNP_ID_132100916 m1A Human chr3 - 47851082 47851082 47851082 TGAAAGTGGGAAGGAAACAGGGTTGCGTAGTCAGGAGACACCTCAGGGGCAACAGCACAGGCCCA TGAAAGTGGGAAGGAAACAGGGTTGCGTAGTCGGGAGACACCTCAGGGGCAACAGCACAGGCCCA T C MAP4 Ensembl:ENSG00000047849 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47850848..47851195 26863196 MeRIP-seq:(Medium) rs888134832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5120529,Human_RBP_ID_7202146,Human_RBP_ID_14852233,Human_RBP_ID_17404591,Human_RBP_ID_18169745,Human_RBP_ID_24005878 RMVar_hsa_circ_217783,RMVar_hsa_circ_124585 87078 RMVar_ID_87078 Human_SNP_ID_132100997 m1A Human chr3 - 47851340 47851340 47851340 TCTCCATGTGCAGGGAGGCTGTCCTGGGCCTGACAGGTCCTCCCCCTTTCTGAGGTAGCAGTGCC TCTCCATGTGCAGGGAGGCTGTCCTGGGCCTGGCAGGTCCTCCCCCTTTCTGAGGTAGCAGTGCC T C MAP4 Ensembl:ENSG00000047849 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:47851289..47851490 32194978 MeRIP-seq:(Medium) rs1283097899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782742,Human_RBP_ID_7202149,Human_RBP_ID_8209699,Human_RBP_ID_18006744,Human_RBP_ID_26510271 Human_miRNA_ID_1478886 RMVar_hsa_circ_114442,RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_376576,RMVar_hsa_circ_217784,RMVar_hsa_circ_217785 87079 RMVar_ID_87079 Human_SNP_ID_132101076 m1A Human chr3 + 47851674 47851674 47851674 TCCCGGGATTTCTCCTCACTGCAGCCATCCCAAGGCCTAGCTGGGATGCCCTCTGTGGGCCTTGC TCCCGGGATTTCTCCTCACTGCAGCCATCCCAGGGCCTAGCTGGGATGCCCTCTGTGGGCCTTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:47851601..47852139 32194978 MeRIP-seq:(Medium) rs1344360100 Functional Loss SNV dbSNP153 33..33 33 - - - 87080 RMVar_ID_87080 Human_SNP_ID_132101435 m1A Human chr3 - 47852877 47852877 47852877 AAATGCCAGGGCCCGCACCGACCACGGGGCCGACATTGTCTCCCGCCCCCCACACTTCCCTGGCG AAATGCCAGGGCCCGCACCGACCACGGGGCCGTCATTGTCTCCCGCCCCCCACACTTCCCTGGCG T A MAP4 Ensembl:ENSG00000047849 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr3:47852826..47853025;chr3:47852826..47853000 26863196 MeRIP-seq:(Medium) rs550682622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603273 Human_Splice_Rec_423304,Human_Splice_Rec_423338,Human_Splice_Rec_423428,Human_Splice_Rec_423444 Human_miRNA_ID_2386403,Human_miRNA_ID_2387876,Human_miRNA_ID_2399032,Human_miRNA_ID_3011314,Human_miRNA_ID_3030082 RMVar_hsa_circ_114442,RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_217785 87081 RMVar_ID_87081 Human_SNP_ID_132102757 m1A Human chr3 - 47857539 47857539 47857539 GGGTTGGCTCTGACAGTATACCTTCTCTCTGAATGAGTCTTTTGTGTCCTTCTCTTCAGGTTCAG GGGTTGGCTCTGACAGTATACCTTCTCTCTGAGTGAGTCTTTTGTGTCCTTCTCTTCAGGTTCAG T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:47857537..47857740 26863196 MeRIP-seq:(Medium) rs769875799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22676352 RMVar_hsa_circ_114442,RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_42607,RMVar_hsa_circ_81267,RMVar_hsa_circ_217785,RMVar_hsa_circ_274956,RMVar_hsa_circ_340061,RMVar_hsa_circ_98216,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,RMVar_hsa_circ_74012,RMVar_hsa_circ_217786,RMVar_hsa_circ_365906,RMVar_hsa_circ_90786,RMVar_hsa_circ_217788,RMVar_hsa_circ_217789 87082 RMVar_ID_87082 Human_SNP_ID_132106385 m1A Human chr3 - 47870875 47870875 47870875 GCCTGGCCACCAATACTTCTGCTCCTGATCTGAAGAATGTCCGCTCCAAGGTTGGCTCCACGGAA GCCTGGCCACCAATACTTCTGCTCCTGATCTGCAGAATGTCCGCTCCAAGGTTGGCTCCACGGAA T G MAP4 Ensembl:ENSG00000047849 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47870801..47871075 26863196 MeRIP-seq:(Medium) rs1257508256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603280,Human_RBP_ID_1964008,Human_RBP_ID_3965112,Human_RBP_ID_5133407,Human_RBP_ID_9261124,Human_RBP_ID_9394893,Human_RBP_ID_14852541,Human_RBP_ID_17292373,Human_RBP_ID_17404596,Human_RBP_ID_18194559,Human_RBP_ID_18809555 Human_Splice_Rec_423297,Human_Splice_Rec_423329,Human_Splice_Rec_423367,Human_Splice_Rec_423403,Human_Splice_Rec_423421,Human_Splice_Rec_423437,Human_Splice_Rec_423457 Human_miRNA_ID_2614575 RMVar_hsa_circ_114442,RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_217792,RMVar_hsa_circ_81267,RMVar_hsa_circ_217785,RMVar_hsa_circ_98216,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,RMVar_hsa_circ_74012,RMVar_hsa_circ_217786,RMVar_hsa_circ_365906,RMVar_hsa_circ_90786,RMVar_hsa_circ_217790,RMVar_hsa_circ_217788,RMVar_hsa_circ_217789,RMVar_hsa_circ_325660,RMVar_hsa_circ_271350,RMVar_hsa_circ_65727,RMVar_hsa_circ_289050,RMVar_hsa_circ_366697,RMVar_hsa_circ_305362,RMVar_hsa_circ_356960,RMVar_hsa_circ_77635,RMVar_hsa_circ_363190,RMVar_hsa_circ_217791 87083 RMVar_ID_87083 Human_SNP_ID_132117396 m1A Human chr3 - 47914897 47914897 47914897 AGGAACGGGGAAAAAGTGCAGCTTGCCGGCCGAGGAGGATTCTGTGTTAGAAAAACTAGGGGAAA AGGAACGGGGAAAAAGTGCAGCTTGCCGGCCGGGGAGGATTCTGTGTTAGAAAAACTAGGGGAAA T C MAP4 Ensembl:ENSG00000047849 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:47914849..47916011 32194978 MeRIP-seq:(Medium) rs142794330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834571,Human_RBP_ID_1069015,Human_RBP_ID_5120247,Human_RBP_ID_7202331,Human_RBP_ID_8573921,Human_RBP_ID_8872750,Human_RBP_ID_14853159 Human_Splice_Rec_423318,Human_Splice_Rec_423319,Human_Splice_Rec_423354,Human_Splice_Rec_423355,Human_Splice_Rec_423392,Human_Splice_Rec_423393 RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_81267,RMVar_hsa_circ_98216,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,RMVar_hsa_circ_217786,RMVar_hsa_circ_90786,RMVar_hsa_circ_217788,RMVar_hsa_circ_217789,RMVar_hsa_circ_65727,RMVar_hsa_circ_77635,RMVar_hsa_circ_217796,RMVar_hsa_circ_47328,RMVar_hsa_circ_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794,RMVar_hsa_circ_302228,RMVar_hsa_circ_354131,RMVar_hsa_circ_373027,RMVar_hsa_circ_376246,RMVar_hsa_circ_353045,RMVar_hsa_circ_282301,RMVar_hsa_circ_217798,RMVar_hsa_circ_217799,RMVar_hsa_circ_217800,RMVar_hsa_circ_217797 87084 RMVar_ID_87084 Human_SNP_ID_132118010 m1A Human chr3 - 47916855 47916855 47916855 GTGGCCCTGGTTAAGGATGTCAGATGGCCCACAGAAACAGATGTATCTTCAGCCAAGAATGTGGT GTGGCCCTGGTTAAGGATGTCAGATGGCCCACGGAAACAGATGTATCTTCAGCCAAGAATGTGGT T C MAP4 Ensembl:ENSG00000047849 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47916805..47916971 26863196 MeRIP-seq:(Medium) rs747715683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153962,Human_RBP_ID_938018,Human_RBP_ID_1627889,Human_RBP_ID_9261128,Human_RBP_ID_9302281,Human_RBP_ID_9393563,Human_RBP_ID_26346862,Human_RBP_ID_27823237 RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_81267,RMVar_hsa_circ_98216,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,RMVar_hsa_circ_217786,RMVar_hsa_circ_90786,RMVar_hsa_circ_217788,RMVar_hsa_circ_217789,RMVar_hsa_circ_77635,RMVar_hsa_circ_217796,RMVar_hsa_circ_47328,RMVar_hsa_circ_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_217794,RMVar_hsa_circ_302228,RMVar_hsa_circ_354131,RMVar_hsa_circ_376246,RMVar_hsa_circ_353045,RMVar_hsa_circ_282301,RMVar_hsa_circ_217798,RMVar_hsa_circ_217799,RMVar_hsa_circ_217797,RMVar_hsa_circ_25351,RMVar_hsa_circ_269105,RMVar_hsa_circ_331968 87085 RMVar_ID_87085 Human_SNP_ID_132137933 m1A Human chr3 - 47998802 47998802 47998802 ATTAACAGAACCATCTCCAGACATTGAGGGAGAGATAAAGCGGGACTTCATTGCCACACTAGAGG ATTAACAGAACCATCTCCAGACATTGAGGGAGGGATAAAGCGGGACTTCATTGCCACACTAGAGG T C MAP4 Ensembl:ENSG00000047849 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:47998751..47998949;chr3:47998751..47998958 26863196 MeRIP-seq:(Medium) rs1366354998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1964044,Human_RBP_ID_4757170,Human_RBP_ID_7202468,Human_RBP_ID_9302286,Human_RBP_ID_18013294,Human_RBP_ID_18809606,Human_RBP_ID_22457305,Human_RBP_ID_24006056 Human_Splice_Rec_423306,Human_Splice_Rec_423340,Human_Splice_Rec_423380,Human_Splice_Rec_423470,Human_Splice_Rec_423482,Human_Splice_Rec_423490,Human_Splice_Rec_423496,Human_Splice_Rec_423502 RMVar_hsa_circ_330,RMVar_hsa_circ_47328,RMVar_hsa_circ_217806,RMVar_hsa_circ_361472,RMVar_hsa_circ_39119,RMVar_hsa_circ_278026,RMVar_hsa_circ_217811,RMVar_hsa_circ_285467,RMVar_hsa_circ_346169,RMVar_hsa_circ_217812 87086 RMVar_ID_87086 Human_SNP_ID_132137957 m1A Human chr3 - 47998877 47998877 47998877 TACATGAAAGATCTTTTTCCTCTTCACCAGGCAGTTGCAGTGGTGCAGAATGGCTGACCTCAGTC TACATGAAAGATCTTTTTCCTCTTCACCAGGCGGTTGCAGTGGTGCAGAATGGCTGACCTCAGTC T C MAP4 Ensembl:ENSG00000047849 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr3:47998851..47998900;chr3:47998828..47998905 26863196 MeRIP-seq:(Medium) rs369521363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757170,Human_RBP_ID_8874996,Human_RBP_ID_9302287,Human_RBP_ID_9394906 Human_Splice_Rec_423306,Human_Splice_Rec_423340,Human_Splice_Rec_423380,Human_Splice_Rec_423470,Human_Splice_Rec_423482,Human_Splice_Rec_423490,Human_Splice_Rec_423496,Human_Splice_Rec_423502 RMVar_hsa_circ_330,RMVar_hsa_circ_47328,RMVar_hsa_circ_217806,RMVar_hsa_circ_361472,RMVar_hsa_circ_39119,RMVar_hsa_circ_278026,RMVar_hsa_circ_217811,RMVar_hsa_circ_285467,RMVar_hsa_circ_346169,RMVar_hsa_circ_217812 87087 RMVar_ID_87087 Human_SNP_ID_132155020 m1A Human chr3 - 48064338 48064338 48064338 TGTGCTGAGTCAGTTCCTGGGTGGGGGCCACAAGACAAGATAGGCCAGTTTATATCAGTCTGGGT TGTGCTGAGTCAGTTCCTGGGTGGGGGCCACAGGACAAGATAGGCCAGTTTATATCAGTCTGGGT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48064335..48064436 26863196 MeRIP-seq:(Medium) rs1260497213 Functional Loss SNV dbSNP153 33..33 33 - - - 87088 RMVar_ID_87088 Human_SNP_ID_132160907 m1A Human chr3 - 48087479 48087479 48087479 TAGACAGAGAAATGGGTGTGGTGAGGGAATACAGCTGCTCTAGGCCTTTGGGGTAACACTGCCCA TAGACAGAGAAATGGGTGTGGTGAGGGAATACGGCTGCTCTAGGCCTTTGGGGTAACACTGCCCA T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48087477..48087586 26863196 MeRIP-seq:(Medium) rs977579100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5325217,Human_RBP_ID_5654594,Human_RBP_ID_8124778,Human_RBP_ID_9435316,Human_RBP_ID_18500066,Human_RBP_ID_23287980,Human_RBP_ID_24006197 87089 RMVar_ID_87089 Human_SNP_ID_132160913 m1A Human chr3 - 48087502 48087501 48087503 AGGGTGCCGTCAGCTTGGCTGGGTAGACAGAGAAATGGGTGTGGTGAGGGAATACAGCTGCTCTA AGGGTGCCGTCAGCTTGGCTGGGTAGACAGA__AATGGGTGTGGTGAGGGAATACAGCTGCTCTA TTC T MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48087494..48087584 26863196 MeRIP-seq:(Medium) rs1477975903 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3720779,Human_RBP_ID_5654333,Human_RBP_ID_8124778,Human_RBP_ID_9435316,Human_RBP_ID_18500066,Human_RBP_ID_23287980,Human_RBP_ID_24006198 87090 RMVar_ID_87090 Human_SNP_ID_132161223 m1A Human chr3 - 48088241 48088241 48088241 GCGGGGCTCTTCCCCCTTGCAAAGGCCCCGACACTGTGTGGGGACTAAAGCGTGTGTCTGGCAGT GCGGGGCTCTTCCCCCTTGCAAAGGCCCCGACGCTGTGTGGGGACTAAAGCGTGTGTCTGGCAGT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48088238..48088614 26863196 MeRIP-seq:(Medium) rs1559931167 Functional Loss SNV dbSNP153 33..33 33 - - - 87091 RMVar_ID_87091 Human_SNP_ID_132161423 m1A Human chr3 + 48088855 48088855 48088855 GGAAGAGCCGTGAGGAGGTAGGAGACGTCGGGAGGAGCCGGGAGCCAGCGAGCTAGCCGGAGGGG GGAAGAGCCGTGAGGAGGTAGGAGACGTCGGGGGGAGCCGGGAGCCAGCGAGCTAGCCGGAGGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:48088700..48088875 26863196 MeRIP-seq:(Medium) rs1473131373 Functional Loss SNV dbSNP153 33..33 33 - - - 87092 RMVar_ID_87092 Human_SNP_ID_132186174 m1A Human chr3 - 48187922 48187922 48187922 CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCACCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCGCCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC T C CDC25A Ensembl:ENSG00000164045 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48187826..48188290 26863410 MeRIP-seq:(Medium) rs994319712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22456582 87093 RMVar_ID_87093 Human_SNP_ID_132186175 m1A Human chr3 - 48187922 48187922 48187922 CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCACCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCCCCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC T G CDC25A Ensembl:ENSG00000164045 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48187826..48188290 26863410 MeRIP-seq:(Medium) rs994319712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22456582 87094 RMVar_ID_87094 Human_SNP_ID_132207629 m1A Human chr3 - 48273270 48273270 48273270 GAATTGTTGGATATAAAATGCTCTAGGATGAAATGCTCGGTGCCATGAAGTAAAACCAGCACTCA GAATTGTTGGATATAAAATGCTCTAGGATGAACTGCTCGGTGCCATGAAGTAAAACCAGCACTCA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:48273192..48273392 26863196 MeRIP-seq:(Medium) rs1432506902 Functional Loss SNV dbSNP153 33..33 33 - - - 87095 RMVar_ID_87095 Human_SNP_ID_132207949 m1A Human chr3 + 48274544 48274544 48274544 CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCACCAGGTCGCTTTTGCTGGGCTAGTAACATCAA CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCGCCAGGTCGCTTTTGCTGGGCTAGTAACATCAA A G ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6442112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18006898 GWAS_ID_10674,GWAS_ID_10675,GWAS_ID_10676,GWAS_ID_10677,GWAS_ID_10678,GWAS_ID_10679,GWAS_ID_10680,GWAS_ID_10681 87096 RMVar_ID_87096 Human_SNP_ID_132207950 m1A Human chr3 + 48274544 48274544 48274544 CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCACCAGGTCGCTTTTGCTGGGCTAGTAACATCAA CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCTCCAGGTCGCTTTTGCTGGGCTAGTAACATCAA A T ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6442112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18006898 GWAS_ID_10674,GWAS_ID_10675,GWAS_ID_10676,GWAS_ID_10677,GWAS_ID_10678,GWAS_ID_10679,GWAS_ID_10680,GWAS_ID_10681 87097 RMVar_ID_87097 Human_SNP_ID_132213900 m1A Human chr3 + 48301317 48301317 48301317 CCTAAGCCCACCCCAGATTCTGGGTCATTCGGAGCCCCAGTGCAGCAGAAGTCCGGCTGCGGGTT CCTAAGCCCACCCCAGATTCTGGGTCATTCGGTGCCCCAGTGCAGCAGAAGTCCGGCTGCGGGTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48301085..48301320 26863196 MeRIP-seq:(Medium) rs1163383587 Functional Loss SNV dbSNP153 33..33 33 - - - 87098 RMVar_ID_87098 Human_SNP_ID_132213992 m1A Human chr3 + 48301519 48301519 48301519 TGTGAGTTGCCCTGGAGGGTGGCGGGTTTTCCAGGCGCATGCATTTGCCGCGGACGGGACGAGAG TGTGAGTTGCCCTGGAGGGTGGCGGGTTTTCCCGGCGCATGCATTTGCCGCGGACGGGACGAGAG A C HSALNG0025823 RNACentral:URS0000EB462F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48301436..48302180 26863196 MeRIP-seq:(Medium) rs1220622183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24498210 87099 RMVar_ID_87099 Human_SNP_ID_132213996 m1A Human chr3 + 48301525 48301525 48301525 TTGCCCTGGAGGGTGGCGGGTTTTCCAGGCGCATGCATTTGCCGCGGACGGGACGAGAGGATGAA TTGCCCTGGAGGGTGGCGGGTTTTCCAGGCGCGTGCATTTGCCGCGGACGGGACGAGAGGATGAA A G HSALNG0025823 RNACentral:URS0000EB462F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48301474..48302180 26863196 MeRIP-seq:(Medium) rs572916273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24498210 87100 RMVar_ID_87100 Human_SNP_ID_132238588 m1A Human chr3 + 48410962 48410962 48410962 AGCATCTTCTCCTTTGCCTGGGAGATGGTGTCACAGTCTAGGACCTTCACGGGCACGCCCTGGGC AGCATCTTCTCCTTTGCCTGGGAGATGGTGTCGCAGTCTAGGACCTTCACGGGCACGCCCTGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48410913..48411940 32194978 MeRIP-seq:(Medium) rs771949296 Functional Loss SNV dbSNP153 33..33 33 - - - 87101 RMVar_ID_87101 Human_SNP_ID_132239557 m1A Human chr3 + 48414015 48414015 48414015 TGCCGCGTCAGCGTCTTCACCACACAGGGGCCATCCCCTATCATAGCCACCACCTCCTCCTTGGA TGCCGCGTCAGCGTCTTCACCACACAGGGGCCGTCCCCTATCATAGCCACCACCTCCTCCTTGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48413753..48414831 32194978 MeRIP-seq:(Medium) rs368174574 Functional Loss SNV dbSNP153 33..33 33 - - - 87102 RMVar_ID_87102 Human_SNP_ID_132240969 m1A Human chr3 + 48418478 48418478 48418478 CACCATGCAGCCCCTCAGCACTGTCCACACGCAGACGGCCGGCCCGACGCAGAAACAGCCCCACA CACCATGCAGCCCCTCAGCACTGTCCACACGCGGACGGCCGGCCCGACGCAGAAACAGCCCCACA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48417934..48419323 32194978 MeRIP-seq:(Medium) rs970412716 Functional Loss SNV dbSNP153 33..33 33 - - - 87103 RMVar_ID_87103 Human_SNP_ID_132241540 m1A Human chr3 + 48419918 48419918 48419918 CACTGCTGCTACCTCTGAGGGTGACAGCGGGGAGGCCAAGAGGTCCTCAGGTGTGGCTGAGGGTC CACTGCTGCTACCTCTGAGGGTGACAGCGGGGGGGCCAAGAGGTCCTCAGGTGTGGCTGAGGGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48419869..48419980 26863196 MeRIP-seq:(Medium) rs1436614844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217846 87104 RMVar_ID_87104 Human_SNP_ID_132242817 m1A Human chr3 + 48423745 48423745 48423745 GCCGAGGAGAAAGCTGCAAAGAGCACCTCCCCATGCGCCACCTCCCTGGACGTGGCCACAGCTGC GCCGAGGAGAAAGCTGCAAAGAGCACCTCCCCTTGCGCCACCTCCCTGGACGTGGCCACAGCTGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48423694..48423795 32194978 MeRIP-seq:(Medium) rs746250691 Functional Loss SNV dbSNP153 33..33 33 - - - 87105 RMVar_ID_87105 Human_SNP_ID_132243992 m1A Human chr3 + 48427643 48427643 48427643 CTCTCCCACCCGATCCATGCCAGTGCTCCCCCACACATGCCCTTCGTTCCTGCCAGCCTGAACTG CTCTCCCACCCGATCCATGCCAGTGCTCCCCCGCACATGCCCTTCGTTCCTGCCAGCCTGAACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48427502..48427859 26863196 MeRIP-seq:(Medium) rs1417323382 Functional Loss SNV dbSNP153 33..33 33 - - - 87106 RMVar_ID_87106 Human_SNP_ID_132244018 m1A Human chr3 - 48427713 48427713 48427713 ATAGCGAGGGAGTGGGCATTCCAGGCAGCGGCAAGAGCCTGTGCAGCGGTTGGAGGAGCCAAGCA ATAGCGAGGGAGTGGGCATTCCAGGCAGCGGCCAGAGCCTGTGCAGCGGTTGGAGGAGCCAAGCA T G PLXNB1 Ensembl:ENSG00000164050 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48427662..48427837 26863196 MeRIP-seq:(Medium) rs891028272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3720782,Human_RBP_ID_3963954,Human_RBP_ID_5654341,Human_RBP_ID_8209261,Human_RBP_ID_8729833,Human_RBP_ID_9435323,Human_RBP_ID_18424193,Human_RBP_ID_18499674,Human_RBP_ID_24382257 87107 RMVar_ID_87107 Human_SNP_ID_132244187 m1A Human chr3 + 48428432 48428432 48428432 CTGGAGTCTCTTCTGGGGCCACCCTACTCTGAACCTTTTCAGGGGGCGCAAGACTGCCCAACTTC CTGGAGTCTCTTCTGGGGCCACCCTACTCTGAGCCTTTTCAGGGGGCGCAAGACTGCCCAACTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48428401..48428527 32194978 MeRIP-seq:(Medium) rs781719378 Functional Loss SNV dbSNP153 33..33 33 - - - 87108 RMVar_ID_87108 Human_SNP_ID_132244495 m1A Human chr3 - 48429469 48429469 48429469 GGGCAGCCCGGCAGGCGAGGGGGAAGGAGCGGAGACGAGCCCGGCCGACGCGGCTTTGTCTCCTT GGGCAGCCCGGCAGGCGAGGGGGAAGGAGCGGGGACGAGCCCGGCCGACGCGGCTTTGTCTCCTT T C PLXNB1 Ensembl:ENSG00000164050 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48429006..48429623 26863196 MeRIP-seq:(Medium) rs1252940454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266515,Human_RBP_ID_1069159,Human_RBP_ID_3721300,Human_RBP_ID_5391576,Human_RBP_ID_8209275,Human_RBP_ID_8236186,Human_RBP_ID_8729759,Human_RBP_ID_9434587,Human_RBP_ID_17208823,Human_RBP_ID_18424200,Human_RBP_ID_18464618,Human_RBP_ID_18953520,Human_RBP_ID_22418225,Human_RBP_ID_22725967,Human_RBP_ID_22745171,Human_RBP_ID_23115810,Human_RBP_ID_24553950,Human_RBP_ID_26790654 87109 RMVar_ID_87109 Human_SNP_ID_132244505 m1A Human chr3 - 48429497 48429497 48429497 GGCCTGGCCCGGGCGGCGGGCGGGGGGAGGGCAGCCCGGCAGGCGAGGGGGAAGGAGCGGAGACG GGCCTGGCCCGGGCGGCGGGCGGGGGGAGGGCGGCCCGGCAGGCGAGGGGGAAGGAGCGGAGACG T C PLXNB1 Ensembl:ENSG00000164050 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:48429454..48429591 26863196 MeRIP-seq:(Medium) rs1330481330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266515,Human_RBP_ID_1069159,Human_RBP_ID_3721301,Human_RBP_ID_5391576,Human_RBP_ID_8209276,Human_RBP_ID_8236186,Human_RBP_ID_8729759,Human_RBP_ID_9434587,Human_RBP_ID_18424200,Human_RBP_ID_18464618,Human_RBP_ID_18953520,Human_RBP_ID_22418225,Human_RBP_ID_22725967,Human_RBP_ID_22745171,Human_RBP_ID_24553950,Human_RBP_ID_26790654 87110 RMVar_ID_87110 Human_SNP_ID_132244674 m1A Human chr3 - 48430009 48430009 48430009 GCGCAGGGGAGAAACAAGGCGCCTTGGAGTTCAGGTAAAGAAAGTTGGGGAGGATGACCACCGGA GCGCAGGGGAGAAACAAGGCGCCTTGGAGTTCGGGTAAAGAAAGTTGGGGAGGATGACCACCGGA T C PLXNB1 Ensembl:ENSG00000164050 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48429853..48430096 26863196 MeRIP-seq:(Medium) rs1414759543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9434589,Human_RBP_ID_18423972,Human_RBP_ID_19115404 Human_Splice_Rec_423923 87111 RMVar_ID_87111 Human_SNP_ID_132245656 m1A Human chr3 - 48433807 48433807 48433807 TGTCCGAGAGGCTCGGGAGGACTTGGAAGTTCACCAGGCCAAGCTGAAGGAGGTGAGGGACCGCT TGTCCGAGAGGCTCGGGAGGACTTGGAAGTTCTCCAGGCCAAGCTGAAGGAGGTGAGGGACCGCT T A CCDC51 Ensembl:ENSG00000164051 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48433146..48433940 26863196 MeRIP-seq:(Medium) rs1479458195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_424282,Human_Splice_Rec_424288,Human_Splice_Rec_424294,Human_Splice_Rec_424306 RMVar_hsa_circ_123117,RMVar_hsa_circ_217850 87112 RMVar_ID_87112 Human_SNP_ID_132245679 m1A Human chr3 + 48433869 48433869 48433869 ACAAGCCCTCGAGCCACCATGAACACTTTCTCAGCCTGCAAAGAGAAAACCGGAGGCCATCTGCA ACAAGCCCTCGAGCCACCATGAACACTTTCTCGGCCTGCAAAGAGAAAACCGGAGGCCATCTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48433726..48433929 26863196 MeRIP-seq:(Medium) rs1268898646 Functional Loss SNV dbSNP153 33..33 33 - - - 87113 RMVar_ID_87113 Human_SNP_ID_132245872 m1A Human chr3 + 48434793 48434793 48434793 TTGGCACATTTCCCAAGTCAGAGGGCGGGGCCAGCCACCCCAGCTCCCCTCCTCACCTCTGTCAC TTGGCACATTTCCCAAGTCAGAGGGCGGGGCCGGCCACCCCAGCTCCCCTCCTCACCTCTGTCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48434782..48435145 26863196 MeRIP-seq:(Medium) rs372223794 Functional Loss SNV dbSNP153 33..33 33 - - - 87114 RMVar_ID_87114 Human_SNP_ID_132245901 m1A Human chr3 - 48434866 48434866 48434866 CACAGCCAAGACTTGGTGGGACAGATATGAAGAGTTTGTTGGACTCAACGAGGTTCGAGAGGCCC CACAGCCAAGACTTGGTGGGACAGATATGAAGGGTTTGTTGGACTCAACGAGGTTCGAGAGGCCC T C CCDC51 Ensembl:ENSG00000164051 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:48434785..48435163;chr3:48434774..48435117;chr3:48434766..48435130 26863196 MeRIP-seq:(Medium) rs781471796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1627959,Human_RBP_ID_8574120 Human_Splice_Rec_424281,Human_Splice_Rec_424287,Human_Splice_Rec_424293,Human_Splice_Rec_424299,Human_Splice_Rec_424305 Human_miRNA_ID_2732928,Human_miRNA_ID_2904094 RMVar_hsa_circ_123117,RMVar_hsa_circ_217850 87115 RMVar_ID_87115 Human_SNP_ID_132246802 m1A Human chr3 - 48438798 48438798 48438798 AAGTGGGGAACCATTGTAGAGGTTGAGCAGAGAGACAATGGTTCCACCTGTGTTTGGAAAGGAAC AAGTGGGGAACCATTGTAGAGGTTGAGCAGAGCGACAATGGTTCCACCTGTGTTTGGAAAGGAAC T G CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48438796..48439164 26863196 MeRIP-seq:(Medium) rs572711794 Functional Loss SNV dbSNP153 33..33 33 - - - 87116 RMVar_ID_87116 Human_SNP_ID_132247081 m1A Human chr3 - 48439919 48439919 48439919 AAGCTCGTCGCTTTCCTGGAACCAAGGAAAGCACAGCTTGGGTGGAGGGAGATTAGGCGGGGAGA AAGCTCGTCGCTTTCCTGGAACCAAGGAAAGCGCAGCTTGGGTGGAGGGAGATTAGGCGGGGAGA T C CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48439916..48440069 26863196 MeRIP-seq:(Medium) rs1209075725 Functional Loss SNV dbSNP153 33..33 33 - - - 87117 RMVar_ID_87117 Human_SNP_ID_132247271 m1A Human chr3 + 48440310 48440310 48440310 GGAAGCGGCGGCAGGCGCCATGTCCGGCCGCGAAGGTAAGTGTTCCGGAACCGTGAGGACTGCGG GGAAGCGGCGGCAGGCGCCATGTCCGGCCGCGCAGGTAAGTGTTCCGGAACCGTGAGGACTGCGG A C TMA7 Ensembl:ENSG00000232112 Protein coding exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:48440276..48440382 26863410 MeRIP-seq:(Medium) rs773665734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784914,Human_RBP_ID_4757179,Human_RBP_ID_5120254,Human_RBP_ID_17660869,Human_RBP_ID_19117348,Human_RBP_ID_22457307 Human_Splice_Rec_424309,Human_Splice_Rec_424311 87118 RMVar_ID_87118 Human_SNP_ID_132249464 m1A Human chr3 + 48446976 48446976 48446976 GGCCCGGGGCTTCTCCGCAGCCGCTGCCCCGGACCCTGACGACCCGTTCGGCGCGCATGGGGACT GGCCCGGGGCTTCTCCGCAGCCGCTGCCCCGGCCCCTGACGACCCGTTCGGCGCGCATGGGGACT A C ATRIP Ensembl:ENSG00000164053 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48446798..48447106 26863410 MeRIP-seq:(Medium) rs200647747 Functional Loss SNV dbSNP153 33..33 33 - - - 87119 RMVar_ID_87119 Human_SNP_ID_132253912 m1A Human chr3 + 48464643 48464643 48464643 GCAGAGCCCCTTGCCCCCAGTCACTGGCTCCAACTGCCAGTGTAATGTGGAGGTGAGTGGGTAGG GCAGAGCCCCTTGCCCCCAGTCACTGGCTCCAGCTGCCAGTGTAATGTGGAGGTGAGTGGGTAGG A G lnc-SHISA5-2 RNACentral:URS00009AD9C9 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1375106252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603453 87120 RMVar_ID_87120 Human_SNP_ID_132254420 m1A Human chr3 + 48466282 48466282 48466282 GCGAGAGCCGCGGGAGAGTGTGCAGCCGAGTCACTACTGCCTGCCTGCCTGCCTGCTACGGTGAG GCGAGAGCCGCGGGAGAGTGTGCAGCCGAGTCGCTACTGCCTGCCTGCCTGCCTGCTACGGTGAG A G TREX1,ATRIP Ensembl:ENSG00000213689,Ensembl:ENSG00000164053 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48466070..48466434 26863196 MeRIP-seq:(Medium) rs1448718323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_424465,Human_Splice_Rec_424507,Human_Splice_Rec_424514,Human_Splice_Rec_424515,Human_Splice_Rec_424519,Human_Splice_Rec_424521,Human_Splice_Rec_424523,Human_Splice_Rec_424525 Human_miRNA_ID_2173066,Human_miRNA_ID_2176510,Human_miRNA_ID_2279149,Human_miRNA_ID_2355004,Human_miRNA_ID_2459211,Human_miRNA_ID_2639447 RMVar_hsa_circ_217855,RMVar_hsa_circ_120796 87121 RMVar_ID_87121 Human_SNP_ID_132254432 m1A Human chr3 + 48466307 48466307 48466307 CCGAGTCACTACTGCCTGCCTGCCTGCCTGCTACGGTGAGTGTGGCCCCCACAATGGGATGGCGC CCGAGTCACTACTGCCTGCCTGCCTGCCTGCTGCGGTGAGTGTGGCCCCCACAATGGGATGGCGC A G TREX1,ATRIP Ensembl:ENSG00000213689,Ensembl:ENSG00000164053 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48466278..48466358 26863196 MeRIP-seq:(Medium) rs1438132078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_424465,Human_Splice_Rec_424507,Human_Splice_Rec_424514,Human_Splice_Rec_424515,Human_Splice_Rec_424519,Human_Splice_Rec_424521,Human_Splice_Rec_424523,Human_Splice_Rec_424525 RMVar_hsa_circ_217855,RMVar_hsa_circ_120796 87122 RMVar_ID_87122 Human_SNP_ID_132255348 m1A Human chr3 + 48468539 48468537 48468540 AACAGGCATGACAGGCTCCAGGGAGCAATGGGACATCTGCCCAAAGGATCAAAGTCCAACTTGGC AACAGGCATGACAGGCTCCAGGGAGCAATGG___ATCTGCCCAAAGGATCAAAGTCCAACTTGGC GGAC G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48468326..48469237 32194978 MeRIP-seq:(Medium) rs1208715700 Functional Loss DEL dbSNP153 32..34 33 - - - 87123 RMVar_ID_87123 Human_SNP_ID_132255588 m1A Human chr3 + 48469132 48469132 48469132 GGAATGCTCAGAGGGCCGCCTTCGGGGCATCCATGTAGGCCGGGTTGTAAGGAGGCTGGCTGGCG GGAATGCTCAGAGGGCCGCCTTCGGGGCATCCGTGTAGGCCGGGTTGTAAGGAGGCTGGCTGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48468991..48469286 26863196 MeRIP-seq:(Medium) rs1223513848 Functional Loss SNV dbSNP153 33..33 33 - - - 87124 RMVar_ID_87124 Human_SNP_ID_132255762 m1A Human chr3 - 48469554 48469554 48469554 ATTCTCTTTGCAGCGGTTGTCACCACCACCACATCCACCACTGTGGTGCATGCCCCTTATCCTCA ATTCTCTTTGCAGCGGTTGTCACCACCACCACGTCCACCACTGTGGTGCATGCCCCTTATCCTCA T C SHISA5 Ensembl:ENSG00000164054 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48469351..48469633 32194978 MeRIP-seq:(Medium) rs774741329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5474897,Human_RBP_ID_17290402,Human_RBP_ID_17403729,Human_RBP_ID_17520212,Human_RBP_ID_18006976,Human_RBP_ID_18953526,Human_RBP_ID_22423448,Human_RBP_ID_22509631 Human_Splice_Rec_424536,Human_Splice_Rec_424546,Human_Splice_Rec_424556,Human_Splice_Rec_424560,Human_Splice_Rec_424566,Human_Splice_Rec_424570,Human_Splice_Rec_424576,Human_Splice_Rec_424580,Human_Splice_Rec_424592,Human_Splice_Rec_424602,Human_Splice_Rec_424612,Human_Splice_Rec_424624,Human_Splice_Rec_424634 Human_miRNA_ID_1994718,Human_miRNA_ID_2054902,Human_miRNA_ID_2227214,Human_miRNA_ID_2503190,Human_miRNA_ID_2753264,Human_miRNA_ID_2755196 RMVar_hsa_circ_326333,RMVar_hsa_circ_351627 87125 RMVar_ID_87125 Human_SNP_ID_132256686 m1A Human chr3 - 48473058 48473057 48473058 AAACTGAGTGGCCCACGATGGGAAGAGGGGAAAGCCCAGGGGTACAGGAGGCCTCTGGGTGAAGG AAACTGAGTGGCCCACGATGGGAAGAGGGGAA_GCCCAGGGGTACAGGAGGCCTCTGGGTGAAGG CT C SHISA5 Ensembl:ENSG00000164054 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48472949..48473116 26863196 MeRIP-seq:(Medium) rs113670805 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_247662,Human_RBP_ID_783808,Human_RBP_ID_5120540,Human_RBP_ID_17291380,Human_RBP_ID_18194564,Human_RBP_ID_22455801 Human_Splice_Rec_424563,Human_Splice_Rec_424567,Human_Splice_Rec_424615,Human_Splice_Rec_424617 RMVar_hsa_circ_351627 87126 RMVar_ID_87126 Human_SNP_ID_132264907 m1A Human chr3 + 48504039 48504039 48504039 CCCCCGGCTCACCACCCGGAGGCGGCGTTAGCAGCAGCAGCAACAGCAACGGCAACAGGATCCGC CCCCCGGCTCACCACCCGGAGGCGGCGTTAGCGGCAGCAGCAACAGCAACGGCAACAGGATCCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48504027..48504122 26863196 MeRIP-seq:(Medium) rs1278340955 Functional Loss SNV dbSNP153 33..33 33 - - - 87127 RMVar_ID_87127 Human_SNP_ID_132264938 m1A Human chr3 - 48504098 48504098 48504098 GCGCTCGCGTCCGTCCGCCCGTCCGCCCGCCCAGCCATGACTGCGCCGGTCCCCGCGCCGCGGAT GCGCTCGCGTCCGTCCGCCCGTCCGCCCGCCCGGCCATGACTGCGCCGGTCCCCGCGCCGCGGAT T C SHISA5 Ensembl:ENSG00000164054 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48504048..48504133 26863196 MeRIP-seq:(Medium) rs914487944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757186 Human_Splice_Rec_424539,Human_Splice_Rec_424605,Human_Splice_Rec_424625,Human_Splice_Rec_424635,Human_Splice_Rec_424643,Human_Splice_Rec_424651 87128 RMVar_ID_87128 Human_SNP_ID_132268453 m1A Human chr3 + 48518426 48518426 48518426 AAGGACTTGGGATCCAGGGGCCTGGCTTCCCCAGAGTCCACCTGTGGACAGCAGGGCACCCGATT AAGGACTTGGGATCCAGGGGCCTGGCTTCCCCGGAGTCCACCTGTGGACAGCAGGGCACCCGATT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48518229..48518776 32194978 MeRIP-seq:(Medium) rs982353992 Functional Loss SNV dbSNP153 33..33 33 - - - 87129 RMVar_ID_87129 Human_SNP_ID_132277448 m1A Human chr3 + 48556449 48556449 48556449 GATGGTGGCCAGACCTAGCCACCGCCAAGCCGATATGCCCCCACACACCTGTCCCCGCCCCCTGC GATGGTGGCCAGACCTAGCCACCGCCAAGCCGGTATGCCCCCACACACCTGTCCCCGCCCCCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48556444..48556782 26863196 MeRIP-seq:(Medium) rs1198555829 Functional Loss SNV dbSNP153 33..33 33 - - - 87130 RMVar_ID_87130 Human_SNP_ID_132277557 m1A Human chr3 + 48556790 48556790 48556790 AATTCCCGTGGGGACGCCATCCCGGGGCCGGGATGAGTCGGACTGCGCCGCTTCCAACCCAGCAG AATTCCCGTGGGGACGCCATCCCGGGGCCGGGGTGAGTCGGACTGCGCCGCTTCCAACCCAGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48556744..48556945 26863196 MeRIP-seq:(Medium) rs1249880349 Functional Loss SNV dbSNP153 33..33 33 - - - 87131 RMVar_ID_87131 Human_SNP_ID_132279853 m1A Human chr3 - 48565159 48565159 48565159 CCCTGAGGATGATGAGTACTCTGAATACTCCGAGTATTCTGTGGAGGAGTACCAGGACCCTGAAG CCCTGAGGATGATGAGTACTCTGAATACTCCGCGTATTCTGTGGAGGAGTACCAGGACCCTGAAG T G COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48565101..48565200 26863196 MeRIP-seq:(Medium) rs1465940042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66956,Human_RBP_ID_5602549,Human_RBP_ID_8574234 Human_Splice_Rec_425066,Human_Splice_Rec_425067,Human_Splice_Rec_425298,Human_Splice_Rec_425299,Human_Splice_Rec_425303 RMVar_hsa_circ_102347,RMVar_hsa_circ_124934,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_217869,RMVar_hsa_circ_217875 87132 RMVar_ID_87132 Human_SNP_ID_132281481 m1A Human chr3 + 48569889 48569889 48569889 CAGGACCTTCCCCACGTTCCTACCTTCTCCCCACGCTCTCCCCTGCTGCCAGGGGGCCCCTGTGT CAGGACCTTCCCCACGTTCCTACCTTCTCCCCCCGCTCTCCCCTGCTGCCAGGGGGCCCCTGTGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48568760..48570525 26863196 MeRIP-seq:(Medium) rs886306814 Functional Loss SNV dbSNP153 33..33 33 - - - 87133 RMVar_ID_87133 Human_SNP_ID_132281607 m1A Human chr3 - 48570280 48570280 48570280 CTGGGCCCCGAGGCGAGCGTGGGGAGCCAGGCATCCGGGTACGTATGTCTTACTCCACAGCCGAA CTGGGCCCCGAGGCGAGCGTGGGGAGCCAGGCGTCCGGGTACGTATGTCTTACTCCACAGCCGAA T C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:48570126..48570350 26863196 MeRIP-seq:(Medium) rs1377514123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19011975 Human_Splice_Rec_425030,Human_Splice_Rec_425031,Human_Splice_Rec_425262,Human_Splice_Rec_425263,Human_Splice_Rec_425330,Human_Splice_Rec_425354,Human_Splice_Rec_425355 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_53352,RMVar_hsa_circ_217878,RMVar_hsa_circ_106133,RMVar_hsa_circ_82782,RMVar_hsa_circ_98848,RMVar_hsa_circ_217879,RMVar_hsa_circ_217880 87134 RMVar_ID_87134 Human_SNP_ID_132281622 m1A Human chr3 + 48570326 48570326 48570326 CGCTCGCCTCGGGGCCCAGGCAGCCCTACTCCAGGGTCTCCCTGGAGACCAACAGGACACCGGGG CGCTCGCCTCGGGGCCCAGGCAGCCCTACTCCCGGGTCTCCCTGGAGACCAACAGGACACCGGGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:48570276..48570421 26863196 MeRIP-seq:(Medium) rs763852342 Functional Loss SNV dbSNP153 33..33 33 - - - 87135 RMVar_ID_87135 Human_SNP_ID_132281623 m1A Human chr3 + 48570326 48570326 48570326 CGCTCGCCTCGGGGCCCAGGCAGCCCTACTCCAGGGTCTCCCTGGAGACCAACAGGACACCGGGG CGCTCGCCTCGGGGCCCAGGCAGCCCTACTCCGGGGTCTCCCTGGAGACCAACAGGACACCGGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:48570276..48570421 26863196 MeRIP-seq:(Medium) rs763852342 Functional Loss SNV dbSNP153 33..33 33 - - - 87136 RMVar_ID_87136 Human_SNP_ID_132281824 m1A Human chr3 + 48570830 48570830 48570830 AGGGCCCCCTCCTCACCCACCATGGATTCACCATGCCCCTACATGCTGTTCCCAGCCCCTCACCC AGGGCCCCCTCCTCACCCACCATGGATTCACCGTGCCCCTACATGCTGTTCCCAGCCCCTCACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48570826..48570971 26863196 MeRIP-seq:(Medium) rs763602386 Functional Loss SNV dbSNP153 33..33 33 - - - 87137 RMVar_ID_87137 Human_SNP_ID_132281825 m1A Human chr3 + 48570830 48570830 48570830 AGGGCCCCCTCCTCACCCACCATGGATTCACCATGCCCCTACATGCTGTTCCCAGCCCCTCACCC AGGGCCCCCTCCTCACCCACCATGGATTCACCTTGCCCCTACATGCTGTTCCCAGCCCCTCACCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48570826..48570971 26863196 MeRIP-seq:(Medium) rs763602386 Functional Loss SNV dbSNP153 33..33 33 - - - 87138 RMVar_ID_87138 Human_SNP_ID_132282059 m1A Human chr3 - 48571496 48571496 48571496 GCTCCCTGTGCCTGTGCCATGCCTGAACTCCCACCTGTCTATGGTAGTATCTGAGCGTCCCTCTG GCTCCCTGTGCCTGTGCCATGCCTGAACTCCCGCCTGTCTATGGTAGTATCTGAGCGTCCCTCTG T C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48571494..48571894 26863196 MeRIP-seq:(Medium) rs536561982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154371,Human_RBP_ID_8574247 Human_Splice_Rec_425343 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_217878,RMVar_hsa_circ_106133,RMVar_hsa_circ_82782,RMVar_hsa_circ_98848,RMVar_hsa_circ_217879,RMVar_hsa_circ_217880,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881 87139 RMVar_ID_87139 Human_SNP_ID_132282060 m1A Human chr3 - 48571496 48571496 48571496 GCTCCCTGTGCCTGTGCCATGCCTGAACTCCCACCTGTCTATGGTAGTATCTGAGCGTCCCTCTG GCTCCCTGTGCCTGTGCCATGCCTGAACTCCCCCCTGTCTATGGTAGTATCTGAGCGTCCCTCTG T G COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48571494..48571894 26863196 MeRIP-seq:(Medium) rs536561982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154371,Human_RBP_ID_8574247 Human_Splice_Rec_425343 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_217878,RMVar_hsa_circ_106133,RMVar_hsa_circ_82782,RMVar_hsa_circ_98848,RMVar_hsa_circ_217879,RMVar_hsa_circ_217880,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881 87140 RMVar_ID_87140 Human_SNP_ID_132282268 m1A Human chr3 - 48572128 48572126 48572129 TGACCGAGGACTGCCAGGGCCGCGAGGCGAGAAGGTGAGGTGGGTTGGCCCTGGGGCCTGACTAC TGACCGAGGACTGCCAGGGCCGCGAGGCGAG___GTGAGGTGGGTTGGCCCTGGGGCCTGACTAC CCTT C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:48571951..48575150;chr3:48571926..48574575;chr3:48571884..48573342 26863196 MeRIP-seq:(Medium) rs1560206805 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5602562,Human_RBP_ID_19011983 Human_Splice_Rec_425018,Human_Splice_Rec_425019,Human_Splice_Rec_425248,Human_Splice_Rec_425249 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_217878,RMVar_hsa_circ_106133,RMVar_hsa_circ_82782,RMVar_hsa_circ_98848,RMVar_hsa_circ_217879,RMVar_hsa_circ_217880,RMVar_hsa_circ_121182,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_217882 87141 RMVar_ID_87141 Human_SNP_ID_132285049 m1A Human chr3 - 48580618 48580617 48580618 GGCACCTGGAGTTCGGGGGCCTGTGGGTGAAAAGGGAGACCAGGGAGATCCTGGAGAGGATGGAC GGCACCTGGAGTTCGGGGGCCTGTGGGTGAAA_GGGAGACCAGGGAGATCCTGGAGAGGATGGAC CT C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:48578379..48581175;chr3:48576530..48582642;chr3:48576530..48583399 26863196 MeRIP-seq:(Medium) rs1064793499 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_424946,Human_Splice_Rec_424947,Human_Splice_Rec_425176,Human_Splice_Rec_425177 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_110617,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_217873,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_98848,RMVar_hsa_circ_217880,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_109527,RMVar_hsa_circ_126151,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_217888,RMVar_hsa_circ_101798,RMVar_hsa_circ_217889,RMVar_hsa_circ_217891,RMVar_hsa_circ_265171,RMVar_hsa_circ_84921,RMVar_hsa_circ_121184,RMVar_hsa_circ_217892,RMVar_hsa_circ_217893 87142 RMVar_ID_87142 Human_SNP_ID_132285050 m1A Human chr3 - 48580618 48580618 48580618 GGCACCTGGAGTTCGGGGGCCTGTGGGTGAAAAGGGAGACCAGGGAGATCCTGGAGAGGATGGAC GGCACCTGGAGTTCGGGGGCCTGTGGGTGAAAGGGGAGACCAGGGAGATCCTGGAGAGGATGGAC T C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:48578379..48581175;chr3:48576530..48582642;chr3:48576530..48583399 26863196 MeRIP-seq:(Medium) rs752784966 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_424946,Human_Splice_Rec_424947,Human_Splice_Rec_425176,Human_Splice_Rec_425177 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_110617,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_217873,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_98848,RMVar_hsa_circ_217880,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_109527,RMVar_hsa_circ_126151,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_217888,RMVar_hsa_circ_101798,RMVar_hsa_circ_217889,RMVar_hsa_circ_217891,RMVar_hsa_circ_265171,RMVar_hsa_circ_84921,RMVar_hsa_circ_121184,RMVar_hsa_circ_217892,RMVar_hsa_circ_217893 87143 RMVar_ID_87143 Human_SNP_ID_132287640 m1A Human chr3 - 48587929 48587929 48587929 CCCACCCTCACGCCTGCCCCAGGTGGCCAGGAACAGTCCCGGGTCCTGGGGCCCGAGCTCAGCAG CCCACCCTCACGCCTGCCCCAGGTGGCCAGGAGCAGTCCCGGGTCCTGGGGCCCGAGCTCAGCAG T C COL7A1 Ensembl:ENSG00000114270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48587796..48587955 26863196 MeRIP-seq:(Medium) rs201566458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_425110 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217898,RMVar_hsa_circ_86729,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909 87144 RMVar_ID_87144 Human_SNP_ID_132287692 m1A Human chr3 - 48588054 48588054 48588054 TAAAGTGGGCAGGGTCAGTGAGGATGAGGAAGATCAGTCAGGAGGGTGAACCCAGTTAACAGAGC TAAAGTGGGCAGGGTCAGTGAGGATGAGGAAGTTCAGTCAGGAGGGTGAACCCAGTTAACAGAGC T A COL7A1 Ensembl:ENSG00000114270 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48588042..48588191 26863196 MeRIP-seq:(Medium) rs188850256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858116,Human_RBP_ID_18809826 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217898,RMVar_hsa_circ_86729,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909 87145 RMVar_ID_87145 Human_SNP_ID_132287693 m1A Human chr3 - 48588054 48588054 48588054 TAAAGTGGGCAGGGTCAGTGAGGATGAGGAAGATCAGTCAGGAGGGTGAACCCAGTTAACAGAGC TAAAGTGGGCAGGGTCAGTGAGGATGAGGAAGGTCAGTCAGGAGGGTGAACCCAGTTAACAGAGC T C COL7A1 Ensembl:ENSG00000114270 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48588042..48588191 26863196 MeRIP-seq:(Medium) rs188850256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858116,Human_RBP_ID_18809826 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217898,RMVar_hsa_circ_86729,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909 87146 RMVar_ID_87146 Human_SNP_ID_132287836 m1A Human chr3 - 48588418 48588418 48588418 GGGCCATGGGGGCAGAGCCTCCCTGATTCCTGAGCTTTCTCTCCAGCGCCTGAGGCTCCGCCAGC GGGCCATGGGGGCAGAGCCTCCCTGATTCCTGGGCTTTCTCTCCAGCGCCTGAGGCTCCGCCAGC T C COL7A1 Ensembl:ENSG00000114270 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48588414..48588630 26863196 MeRIP-seq:(Medium) rs1357868765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67001,Human_RBP_ID_19115411,Human_RBP_ID_21986907,Human_RBP_ID_22678568 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_16984,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909 87147 RMVar_ID_87147 Human_SNP_ID_132287978 m1A Human chr3 - 48588773 48588773 48588773 TATGCCCACCTGGCCAGGCGGCCCCATGAGGCACCAGATACTCCCAGGAAACACAGACTCTGCAG TATGCCCACCTGGCCAGGCGGCCCCATGAGGCGCCAGATACTCCCAGGAAACACAGACTCTGCAG T C COL7A1 Ensembl:ENSG00000114270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48588492..48588775 26863196 MeRIP-seq:(Medium) rs1244085666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154374,Human_RBP_ID_22823839 Human_Splice_Rec_425106 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_16984,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909,RMVar_hsa_circ_217912,RMVar_hsa_circ_75728 87148 RMVar_ID_87148 Human_SNP_ID_132288068 m1A Human chr3 + 48588991 48588991 48588991 ATCTGCAGCCTCGACACACGACCCACAGGCTCAGGGGCTGGGGACAGAGGCAAGGTAAGGGGTCC ATCTGCAGCCTCGACACACGACCCACAGGCTCGGGGGCTGGGGACAGAGGCAAGGTAAGGGGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48588865..48589010 26863196 MeRIP-seq:(Medium) rs947119289 Functional Loss SNV dbSNP153 33..33 33 - - - 87149 RMVar_ID_87149 Human_SNP_ID_132289115 m1A Human chr3 + 48592134 48592134 48592134 CAGTGCGAGCCATCAGGGAAGTGGCGGGCCCCACACTGCGGCCAAATAGGGTGCTCACGGTCACC CAGTGCGAGCCATCAGGGAAGTGGCGGGCCCCCCACTGCGGCCAAATAGGGTGCTCACGGTCACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48591997..48592196 26863196 MeRIP-seq:(Medium) rs924073820 Functional Loss SNV dbSNP153 33..33 33 - - - 87150 RMVar_ID_87150 Human_SNP_ID_132290134 m1A Human chr3 - 48594982 48594982 48594982 TCGGCCTTCATCCCCAACACCCCCCGCCCACAACCCAGCCAACTCCACGACGCCCCGCGGATTCC TCGGCCTTCATCCCCAACACCCCCCGCCCACAGCCCAGCCAACTCCACGACGCCCCGCGGATTCC T C COL7A1 Ensembl:ENSG00000114270 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:48594975..48595202 26863196 MeRIP-seq:(Medium) rs1021344547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80543,RMVar_hsa_circ_217921 87151 RMVar_ID_87151 Human_SNP_ID_132292497 m1A Human chr3 - 48602897 48602897 48602897 GCAGGAGCAAGGGGGAGCAGTAGATGGACTCCAGGTGGTTTTATAGATGGAACCTGGTTGGGGTC GCAGGAGCAAGGGGGAGCAGTAGATGGACTCCCGGTGGTTTTATAGATGGAACCTGGTTGGGGTC T G UQCRC1 Ensembl:ENSG00000010256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:48602895..48603050;chr3:48602895..48603010 26863196 MeRIP-seq:(Medium) rs890798400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5150341 RMVar_hsa_circ_122197,RMVar_hsa_circ_116876,RMVar_hsa_circ_102894,RMVar_hsa_circ_111089,RMVar_hsa_circ_100636,RMVar_hsa_circ_217925,RMVar_hsa_circ_79147,RMVar_hsa_circ_217927,RMVar_hsa_circ_217926,RMVar_hsa_circ_217923,RMVar_hsa_circ_217924,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_107167,RMVar_hsa_circ_217934,RMVar_hsa_circ_118179,RMVar_hsa_circ_217937,RMVar_hsa_circ_217938,RMVar_hsa_circ_93335,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217941,RMVar_hsa_circ_217942 87152 RMVar_ID_87152 Human_SNP_ID_132292681 m1A Human chr3 - 48603614 48603614 48603614 TAGGAAGCTGTCTCGTGCAGACTTGACCGAGTACCTCAGCACACATTACAAGGCCCCTCGAATGG TAGGAAGCTGTCTCGTGCAGACTTGACCGAGTGCCTCAGCACACATTACAAGGCCCCTCGAATGG T C UQCRC1 Ensembl:ENSG00000010256 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48603524..48603662 26863196 MeRIP-seq:(Medium) rs1359683408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66324,Human_RBP_ID_282761,Human_RBP_ID_933111,Human_RBP_ID_1628023,Human_RBP_ID_18006989,Human_RBP_ID_18809857,Human_RBP_ID_22455808 Human_Splice_Rec_425382,Human_Splice_Rec_425383,Human_Splice_Rec_425410,Human_Splice_Rec_425411,Human_Splice_Rec_425425,Human_Splice_Rec_425438,Human_Splice_Rec_425439,Human_Splice_Rec_425450 Human_miRNA_ID_875764 RMVar_hsa_circ_122197,RMVar_hsa_circ_116876,RMVar_hsa_circ_102894,RMVar_hsa_circ_111089,RMVar_hsa_circ_100636,RMVar_hsa_circ_217925,RMVar_hsa_circ_79147,RMVar_hsa_circ_217927,RMVar_hsa_circ_217926,RMVar_hsa_circ_217923,RMVar_hsa_circ_217924,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_107167,RMVar_hsa_circ_217934,RMVar_hsa_circ_118179,RMVar_hsa_circ_217937,RMVar_hsa_circ_217938,RMVar_hsa_circ_93335,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217941,RMVar_hsa_circ_217942 87153 RMVar_ID_87153 Human_SNP_ID_132293060 m1A Human chr3 - 48604770 48604770 48604770 TCTGGTTGATATCTGGTTCCAGGGAACAAAGAATCGGCCTGGCAGTGCCCTGGAGAAGGAGGTGG TCTGGTTGATATCTGGTTCCAGGGAACAAAGATTCGGCCTGGCAGTGCCCTGGAGAAGGAGGTGG T A UQCRC1 Ensembl:ENSG00000010256 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48604619..48604820 26863196 MeRIP-seq:(Medium) rs1485379708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933113,Human_RBP_ID_3963973,Human_RBP_ID_5120541,Human_RBP_ID_7203240,Human_RBP_ID_8943483,Human_RBP_ID_14858244,Human_RBP_ID_18471789,Human_RBP_ID_22676377 Human_Splice_Rec_425378,Human_Splice_Rec_425406,Human_Splice_Rec_425446,Human_Splice_Rec_425456,Human_Splice_Rec_425462 RMVar_hsa_circ_122197,RMVar_hsa_circ_116876,RMVar_hsa_circ_102894,RMVar_hsa_circ_217925,RMVar_hsa_circ_79147,RMVar_hsa_circ_217923,RMVar_hsa_circ_217924,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_120659,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217942,RMVar_hsa_circ_126119,RMVar_hsa_circ_217944,RMVar_hsa_circ_76431,RMVar_hsa_circ_217945,RMVar_hsa_circ_217943 87154 RMVar_ID_87154 Human_SNP_ID_132294312 m1A Human chr3 - 48609244 48609244 48609244 GCGGAGTACGGCAACCTTCGCTCAGGCGCTCCAGTTCGTGCCGGAGACGCAGGTTAGCCTGCTGG GCGGAGTACGGCAACCTTCGCTCAGGCGCTCCGGTTCGTGCCGGAGACGCAGGTTAGCCTGCTGG T C UQCRC1 Ensembl:ENSG00000010256 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48605751..48609547 32194978 MeRIP-seq:(Medium) rs1377422713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603560,Human_RBP_ID_782674,Human_RBP_ID_1033526,Human_RBP_ID_4756438,Human_RBP_ID_5149708,Human_RBP_ID_8875006,Human_RBP_ID_8943484,Human_RBP_ID_22823884 Human_Splice_Rec_425374,Human_Splice_Rec_425375,Human_Splice_Rec_425442,Human_Splice_Rec_425443,Human_Splice_Rec_425452,Human_Splice_Rec_425453,Human_Splice_Rec_425460,Human_Splice_Rec_425461 RMVar_hsa_circ_102894,RMVar_hsa_circ_79147,RMVar_hsa_circ_217923,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_45708,RMVar_hsa_circ_120659,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217942,RMVar_hsa_circ_217944,RMVar_hsa_circ_76431,RMVar_hsa_circ_217943 87155 RMVar_ID_87155 Human_SNP_ID_132294336 m1A Human chr3 - 48609287 48609287 48609287 GCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGACGCCAGCCTTGCGGAGTACGGCAACCTTCGCT GCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGGCGCCAGCCTTGCGGAGTACGGCAACCTTCGCT T C UQCRC1 Ensembl:ENSG00000010256 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48609176..48609355 26863410 MeRIP-seq:(Medium) rs370111314 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_246970,Human_RBP_ID_603563,Human_RBP_ID_834490,Human_RBP_ID_4745011,Human_RBP_ID_8875497,Human_RBP_ID_8943485,Human_RBP_ID_9302304,Human_RBP_ID_22455810 Human_Splice_Rec_425374,Human_Splice_Rec_425442,Human_Splice_Rec_425452,Human_Splice_Rec_425460 RMVar_hsa_circ_102894,RMVar_hsa_circ_79147,RMVar_hsa_circ_217923,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_45708,RMVar_hsa_circ_120659,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217942,RMVar_hsa_circ_217944,RMVar_hsa_circ_76431,RMVar_hsa_circ_217943 87156 RMVar_ID_87156 Human_SNP_ID_132294346 m1A Human chr3 - 48609304 48609303 48609304 CCGAGTCCTCACTCGCGGCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGACGCCAGCCTTGCGGA CCGAGTCCTCACTCGCGGCTGTTCCCTTCCAC_GCCGGCCCTGCTGCGGACGCCAGCCTTGCGGA CT C UQCRC1 Ensembl:ENSG00000010256 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48609301..48609325 26863196 MeRIP-seq:(Medium) rs762805070 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4765793,Human_RBP_ID_8943485,Human_RBP_ID_27319295 RMVar_hsa_circ_102894,RMVar_hsa_circ_217922,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_120659,RMVar_hsa_circ_217943 87157 RMVar_ID_87157 Human_SNP_ID_132294351 m1A Human chr3 - 48609304 48609304 48609304 CCGAGTCCTCACTCGCGGCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGACGCCAGCCTTGCGGA CCGAGTCCTCACTCGCGGCTGTTCCCTTCCACCGCCGGCCCTGCTGCGGACGCCAGCCTTGCGGA T G UQCRC1 Ensembl:ENSG00000010256 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48609301..48609325 26863196 MeRIP-seq:(Medium) rs1319218440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4765793,Human_RBP_ID_8943485,Human_RBP_ID_27319295 RMVar_hsa_circ_102894,RMVar_hsa_circ_217922,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_120659,RMVar_hsa_circ_217943 87158 RMVar_ID_87158 Human_SNP_ID_132299288 m1A Human chr3 - 48627003 48627003 48627003 GATGGAAGATGCAACAGCCAATGGTCAAGAAGACTCCAAGGCCCCAGATGGGTCCACACTGAAGG GATGGAAGATGCAACAGCCAATGGTCAAGAAGTCTCCAAGGCCCCAGATGGGTCCACACTGAAGG T A SLC26A6 Ensembl:ENSG00000225697 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48626953..48627077 26863196 MeRIP-seq:(Medium) rs376236607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_935203,Human_RBP_ID_9394962,Human_RBP_ID_18471637,Human_RBP_ID_19010227,Human_RBP_ID_22769169,Human_RBP_ID_24547546,Human_RBP_ID_26346870,Human_RBP_ID_27822233 Human_Splice_Rec_425498,Human_Splice_Rec_425536,Human_Splice_Rec_425572,Human_Splice_Rec_425632,Human_Splice_Rec_425670,Human_Splice_Rec_425704,Human_Splice_Rec_425740,Human_Splice_Rec_425776,Human_Splice_Rec_425784 RMVar_hsa_circ_217951,RMVar_hsa_circ_75561 87159 RMVar_ID_87159 Human_SNP_ID_132299863 m1A Human chr3 - 48628824 48628824 48628824 TGGGAGGGCCTGGACTGCAGCCTGGGGAGCAGAGGGCTGGGCGGTGGCAGGCACTGGGCACACTA TGGGAGGGCCTGGACTGCAGCCTGGGGAGCAGGGGGCTGGGCGGTGGCAGGCACTGGGCACACTA T C SLC26A6 Ensembl:ENSG00000225697 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48628774..48629118 26863196 MeRIP-seq:(Medium) rs1263354841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721981 RMVar_hsa_circ_96399,RMVar_hsa_circ_217952 87160 RMVar_ID_87160 Human_SNP_ID_132300523 m1A Human chr3 + 48630798 48630798 48630798 TGGTCACTGTTCCACTGTATCTAGGCCTGTGCATCCCCAATCTCCATCCCCACCAAGTGGCCCCC TGGTCACTGTTCCACTGTATCTAGGCCTGTGCGTCCCCAATCTCCATCCCCACCAAGTGGCCCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48630787..48630964 26863196 MeRIP-seq:(Medium) rs1350027610 Functional Loss SNV dbSNP153 33..33 33 - - - 87161 RMVar_ID_87161 Human_SNP_ID_132301029 m1A Human chr3 - 48632082 48632082 48632082 CTTGCCCTGCGCTCCTCATTAGCAACCCCAGGACCCCTGCCTCTCCTGACTGCCCCTGGCCGCCC CTTGCCCTGCGCTCCTCATTAGCAACCCCAGGCCCCCTGCCTCTCCTGACTGCCCCTGGCCGCCC T G SLC26A6 Ensembl:ENSG00000225697 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48632064..48632163 26863196 MeRIP-seq:(Medium) rs760980882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17088861,Human_RBP_ID_18954341,Human_RBP_ID_25764463 Human_Splice_Rec_425754,Human_Splice_Rec_425886 RMVar_hsa_circ_96399,RMVar_hsa_circ_217952,RMVar_hsa_circ_352899,RMVar_hsa_circ_106787,RMVar_hsa_circ_217955 87162 RMVar_ID_87162 Human_SNP_ID_132301149 m1A Human chr3 - 48632353 48632353 48632353 GTCATGTCTGTGATGGTGGGCAGTGTGACAGAATCCCTGGCCCCGCAGGCCTTGAACGACTCCAT GTCATGTCTGTGATGGTGGGCAGTGTGACAGAGTCCCTGGCCCCGCAGGCCTTGAACGACTCCAT T C SLC26A6 Ensembl:ENSG00000225697 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48632302..48632393 26863196 MeRIP-seq:(Medium) rs1559469732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784286,Human_RBP_ID_936895,Human_RBP_ID_9394971 Human_Splice_Rec_425474,Human_Splice_Rec_425512,Human_Splice_Rec_425548,Human_Splice_Rec_425608,Human_Splice_Rec_425646,Human_Splice_Rec_425716,Human_Splice_Rec_425858 Human_miRNA_ID_2661322,Human_miRNA_ID_2679772,Human_miRNA_ID_3065450 RMVar_hsa_circ_96399,RMVar_hsa_circ_217952,RMVar_hsa_circ_352899,RMVar_hsa_circ_106787,RMVar_hsa_circ_16312,RMVar_hsa_circ_217955 87163 RMVar_ID_87163 Human_SNP_ID_132302019 m1A Human chr3 + 48635311 48635311 48635311 GAATGCCTGCTCCAGCGAGGCGTCGCAAGCGGAGAATGCCTGCTCCAGCGAGGCGCTCGCGCGGG GAATGCCTGCTCCAGCGAGGCGTCGCAAGCGGGGAATGCCTGCTCCAGCGAGGCGCTCGCGCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48635308..48635417 26863196 MeRIP-seq:(Medium) rs1419729977 Functional Loss SNV dbSNP153 33..33 33 - - - 87164 RMVar_ID_87164 Human_SNP_ID_132304262 m1A Human chr3 + 48642910 48642910 48642910 CAGGTCCCTGGGGGTGGTAGGGACAGAGTGTGAGCTAACCCTGAAGCAGCCTAAAACTCTGGCTT CAGGTCCCTGGGGGTGGTAGGGACAGAGTGTGGGCTAACCCTGAAGCAGCCTAAAACTCTGGCTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48642908..48643017 32194978 MeRIP-seq:(Medium) rs1404894041 Functional Loss SNV dbSNP153 33..33 33 - - - 87165 RMVar_ID_87165 Human_SNP_ID_132310418 m1A Human chr3 - 48662789 48662789 48662789 CGCACGCCGGAGGGGCTCCGGCCGCGGAGTAGATGGTGCCCAGAGGGCGGCGGGGGTGCGGAGAG CGCACGCCGGAGGGGCTCCGGCCGCGGAGTAGGTGGTGCCCAGAGGGCGGCGGGGGTGCGGAGAG T C CELSR3 Ensembl:ENSG00000008300 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:48662519..48662876;chr3:48662460..48662947 26863196 MeRIP-seq:(Medium) rs1340105959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2423424,Human_miRNA_ID_2433084 RMVar_hsa_circ_113259,RMVar_hsa_circ_217965 87166 RMVar_ID_87166 Human_SNP_ID_132313576 m1A Human chr3 - 48674263 48674263 48674263 CTTCAGCATGCCCCCCTCTTCACCCCACACCCATGTGTACACTCAGAGTCCTGCTGCCGCTCCAG CTTCAGCATGCCCCCCTCTTCACCCCACACCCGTGTGTACACTCAGAGTCCTGCTGCCGCTCCAG T C NCKIPSD Ensembl:ENSG00000213672 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48674217..48674305 26863196 MeRIP-seq:(Medium) rs776745390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17088598,Human_RBP_ID_18007022,Human_RBP_ID_22823936 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 87167 RMVar_ID_87167 Human_SNP_ID_132315562 m1A Human chr3 + 48680898 48680898 48680898 CTTACTGCCAAGGTCAGCAAGGCACTACCCTCACCCACGCCGTGTCCATTCCTTCCCTGCAGCCA CTTACTGCCAAGGTCAGCAAGGCACTACCCTCCCCCACGCCGTGTCCATTCCTTCCCTGCAGCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48680719..48681072 26863196 MeRIP-seq:(Medium) rs1218764271 Functional Loss SNV dbSNP153 33..33 33 - - - 87168 RMVar_ID_87168 Human_SNP_ID_132315860 m1A Human chr3 - 48681699 48681699 48681699 CTCAGTCAGCAGCACCTCCCTGGACACGCTCTATACCAGCTCCAGCCCATCTGAACCAGGCTCCA CTCAGTCAGCAGCACCTCCCTGGACACGCTCTGTACCAGCTCCAGCCCATCTGAACCAGGCTCCA T C NCKIPSD Ensembl:ENSG00000213672 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48681496..48681781 26863196 MeRIP-seq:(Medium) rs758246917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_425990,Human_Splice_Rec_426014,Human_Splice_Rec_426060,Human_Splice_Rec_426068,Human_Splice_Rec_426076,Human_Splice_Rec_426084 RMVar_hsa_circ_95303,RMVar_hsa_circ_103228,RMVar_hsa_circ_119856,RMVar_hsa_circ_217969,RMVar_hsa_circ_87516,RMVar_hsa_circ_217971,RMVar_hsa_circ_217972,RMVar_hsa_circ_217970 87169 RMVar_ID_87169 Human_SNP_ID_132316138 m1A Human chr3 + 48682373 48682373 48682373 CACACACCTGGTAGAGGCCTCCATCTGCCCCAAGATGCTCAGAACTGGGTAGGCTGTGCTGCCGC CACACACCTGGTAGAGGCCTCCATCTGCCCCAGGATGCTCAGAACTGGGTAGGCTGTGCTGCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48682350..48682443 26863196 MeRIP-seq:(Medium) rs1335863313 Functional Loss SNV dbSNP153 33..33 33 - - - 87170 RMVar_ID_87170 Human_SNP_ID_132317290 m1A Human chr3 + 48685818 48685818 48685818 ACGCGTACAGCGCGCGGTACATGAGGCCGGGCAGGGCAGGTGCAGGGAAGGTGGCAAGGGCTGCG ACGCGTACAGCGCGCGGTACATGAGGCCGGGCGGGGCAGGTGCAGGGAAGGTGGCAAGGGCTGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48685717..48685882 26863410 MeRIP-seq:(Medium) rs1388415421 Functional Loss SNV dbSNP153 33..33 33 - - - 87171 RMVar_ID_87171 Human_SNP_ID_132319442 m1A Human chr3 + 48693732 48693732 48693732 CACAGCACAAGACACCCTAGCAAAGGCTTCCCACAGTGCCCCCACACGGGTAGGCACCCAGGCCT CACAGCACAAGACACCCTAGCAAAGGCTTCCCGCAGTGCCCCCACACGGGTAGGCACCCAGGCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48693681..48693781 32194978 MeRIP-seq:(Medium) rs984705097 Functional Loss SNV dbSNP153 33..33 33 - - - 87172 RMVar_ID_87172 Human_SNP_ID_132319481 m1A Human chr3 - 48693900 48693900 48693900 ACTGTCTTAATTACTCATGGCAGGTTCTAGAGACTTAAGGGGAAAAGCTGCTTTCAAGGCCACCA ACTGTCTTAATTACTCATGGCAGGTTCTAGAGGCTTAAGGGGAAAAGCTGCTTTCAAGGCCACCA T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48693876..48693900 32194978 MeRIP-seq:(Medium) rs1019673686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603646,Human_RBP_ID_1628081,Human_RBP_ID_2788536,Human_RBP_ID_8574378,Human_RBP_ID_9141330,Human_RBP_ID_14858818,Human_RBP_ID_27319411 RMVar_hsa_circ_110457,RMVar_hsa_circ_82807,RMVar_hsa_circ_217975,RMVar_hsa_circ_217976 87173 RMVar_ID_87173 Human_SNP_ID_132319759 m1A Human chr3 + 48694881 48694881 48694881 TCTACCAAAATCAAACTCAAATCCACACAACAAAACAGAATTGAGCAATCTTACCAGGGATTGAA TCTACCAAAATCAAACTCAAATCCACACAACACAACAGAATTGAGCAATCTTACCAGGGATTGAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48694875..48695125 32194978 MeRIP-seq:(Medium) rs1269387316 Functional Loss SNV dbSNP153 33..33 33 - - - 87174 RMVar_ID_87174 Human_SNP_ID_132319760 m1A Human chr3 + 48694881 48694881 48694881 TCTACCAAAATCAAACTCAAATCCACACAACAAAACAGAATTGAGCAATCTTACCAGGGATTGAA TCTACCAAAATCAAACTCAAATCCACACAACAGAACAGAATTGAGCAATCTTACCAGGGATTGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48694875..48695125 32194978 MeRIP-seq:(Medium) rs1269387316 Functional Loss SNV dbSNP153 33..33 33 - - - 87175 RMVar_ID_87175 Human_SNP_ID_132319878 m1A Human chr3 + 48695189 48695189 48695189 GACCAGGGGCTTGCACAGGGTTGTCTCATTGAAGCGGAGCACGCATGAGTGCCCCCCGACCTGGT GACCAGGGGCTTGCACAGGGTTGTCTCATTGACGCGGAGCACGCATGAGTGCCCCCCGACCTGGT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:48695101..48695425 26863196 MeRIP-seq:(Medium) rs139349177 Functional Loss SNV dbSNP153 33..33 33 - - - 87176 RMVar_ID_87176 Human_SNP_ID_132319888 m1A Human chr3 - 48695202 48695202 48695202 GAGCCCTTTGTCCACCAGGTCGGGGGGCACTCATGCGTGCTCCGCTTCAATGAGACAACCCTGTG GAGCCCTTTGTCCACCAGGTCGGGGGGCACTCGTGCGTGCTCCGCTTCAATGAGACAACCCTGTG T C IP6K2 Ensembl:ENSG00000068745 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:48695076..48695425 26863196 MeRIP-seq:(Medium) rs747377400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_282762,Human_RBP_ID_933128,Human_RBP_ID_1628092,Human_RBP_ID_4745141,Human_RBP_ID_9394982,Human_RBP_ID_18182125,Human_RBP_ID_22091680,Human_RBP_ID_22282280,Human_RBP_ID_22509643,Human_RBP_ID_23119983,Human_RBP_ID_26346281 RMVar_hsa_circ_110457,RMVar_hsa_circ_14884,RMVar_hsa_circ_82807,RMVar_hsa_circ_217975,RMVar_hsa_circ_217976,RMVar_hsa_circ_17394 87177 RMVar_ID_87177 Human_SNP_ID_132319969 m1A Human chr3 - 48695401 48695399 48695402 GTTTGCTTCCAGCAGAGCATCCTGGCCAGAACAAGCCAAGGAGCCAAGACGAGAGGGACACACGG GTTTGCTTCCAGCAGAGCATCCTGGCCAGAA___GCCAAGGAGCCAAGACGAGAGGGACACACGG CTTG C IP6K2 Ensembl:ENSG00000068745 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:48695301..48695475 26863410 MeRIP-seq:(Medium) rs1410707152 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_247061,Human_RBP_ID_834657,Human_RBP_ID_9393595,Human_RBP_ID_22551518,Human_RBP_ID_26346883,Human_RBP_ID_27823253 Human_Splice_Rec_426086,Human_Splice_Rec_426106,Human_Splice_Rec_426112,Human_Splice_Rec_426118,Human_Splice_Rec_426124,Human_Splice_Rec_426130,Human_Splice_Rec_426136,Human_Splice_Rec_426140,Human_Splice_Rec_426144,Human_Splice_Rec_426162,Human_Splice_Rec_426166,Human_Splice_Rec_426174,Human_Splice_Rec_426176,Human_Splice_Rec_426180,Human_Splice_Rec_426184,Human_Splice_Rec_426190,Human_Splice_Rec_426192,Human_Splice_Rec_426198,Human_Splice_Rec_426204,Human_Splice_Rec_426208,Human_Splice_Rec_426212,Human_Splice_Rec_426216,Human_Splice_Rec_426222,Human_Splice_Rec_426228,Human_Splice_Rec_426234 RMVar_hsa_circ_110457,RMVar_hsa_circ_14884,RMVar_hsa_circ_82807,RMVar_hsa_circ_217975,RMVar_hsa_circ_217976,RMVar_hsa_circ_17394 87178 RMVar_ID_87178 Human_SNP_ID_132321727 m1A Human chr3 - 48702646 48702646 48702646 TGCCCCAGGGAGTGGCACTCACTTTTAGATAGAGTGGCTGAAGATCCCATTAAAGAGATGACATT TGCCCCAGGGAGTGGCACTCACTTTTAGATAGTGTGGCTGAAGATCCCATTAAAGAGATGACATT T A IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48702643..48702743 26863196 MeRIP-seq:(Medium) rs548761467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859155 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 87179 RMVar_ID_87179 Human_SNP_ID_132321728 m1A Human chr3 - 48702646 48702646 48702646 TGCCCCAGGGAGTGGCACTCACTTTTAGATAGAGTGGCTGAAGATCCCATTAAAGAGATGACATT TGCCCCAGGGAGTGGCACTCACTTTTAGATAGGGTGGCTGAAGATCCCATTAAAGAGATGACATT T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48702643..48702743 26863196 MeRIP-seq:(Medium) rs548761467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859155 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 87180 RMVar_ID_87180 Human_SNP_ID_132325380 m1A Human chr3 + 48717096 48717096 48717096 GACTCCAATGATCAGAGATCCCGTTTCCCAGTAGCCTGAAAAAATCTCCCTCAAAGCTCCTCGGG GACTCCAATGATCAGAGATCCCGTTTCCCAGTGGCCTGAAAAAATCTCCCTCAAAGCTCCTCGGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:48717082..48717204 26863410 MeRIP-seq:(Medium) rs978577178 Functional Loss SNV dbSNP153 33..33 33 - - - 87181 RMVar_ID_87181 Human_SNP_ID_132358039 m1A Human chr3 + 48847688 48847688 48847688 CACTCACGCCGGCCTTTCGCTCCGCGCCCGCGAGGTCTCTTCGCGCACGGCCCCGGCTCACGTCG CACTCACGCCGGCCTTTCGCTCCGCGCCCGCGGGGTCTCTTCGCGCACGGCCCCGGCTCACGTCG A G PRKAR2A-AS1 Ensembl:ENSG00000224424 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:48847346..48847850;chr3:48847312..48847834 26863196 MeRIP-seq:(Medium) rs996765423 Functional Loss SNV dbSNP153 33..33 33 - - - 87182 RMVar_ID_87182 Human_SNP_ID_132370144 m1A Human chr3 + 48898793 48898793 48898793 TGAGCGGGCTGATGGGTTTTGGCTGGTCGGCCATGGTCAGTCCGTCTGTCACTCCGTCTGTCAGT TGAGCGGGCTGATGGGTTTTGGCTGGTCGGCCGTGGTCAGTCCGTCTGTCACTCCGTCTGTCAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:48898742..48898868;chr3:48898753..48898852 26863196 MeRIP-seq:(Medium) rs1358429634 Functional Loss SNV dbSNP153 33..33 33 - - - 87183 RMVar_ID_87183 Human_SNP_ID_132370145 m1A Human chr3 - 48898794 48898794 48898794 AACTGACAGACGGAGTGACAGACGGACTGACCATGGCCGACCAGCCAAAACCCATCAGCCCGCTC AACTGACAGACGGAGTGACAGACGGACTGACCGTGGCCGACCAGCCAAAACCCATCAGCCCGCTC T C SLC25A20 Ensembl:ENSG00000178537 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48898743..48898842 26863196 MeRIP-seq:(Medium) rs745490594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785480,Human_RBP_ID_4757198,Human_RBP_ID_5602620 GWAS_ID_10682 87184 RMVar_ID_87184 Human_SNP_ID_132378129 m1A Human chr3 - 48927586 48927586 48927586 ATTTGGGTCATAGTCCTCTTCATTGCTGTCAGACCCCTGGCTATTCATGTCCACTGACATCTTAG ATTTGGGTCATAGTCCTCTTCATTGCTGTCAGGCCCCTGGCTATTCATGTCCACTGACATCTTAG T C lnc-NCKIPSD-1 RNACentral:URS00008B560A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:48927536..48927726 26863196 MeRIP-seq:(Medium) rs1251780705 Functional Loss SNV dbSNP153 33..33 33 - - - 87185 RMVar_ID_87185 Human_SNP_ID_132378138 m1A Human chr3 - 48927619 48927619 48927619 GTCGTCTTCTTCTTCTTCTTCCTCTTCCTCACAATTTGGGTCATAGTCCTCTTCATTGCTGTCAG GTCGTCTTCTTCTTCTTCTTCCTCTTCCTCACGATTTGGGTCATAGTCCTCTTCATTGCTGTCAG T C lnc-NCKIPSD-1 RNACentral:URS00008B560A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48927569..48927745 26863196 MeRIP-seq:(Medium) rs1172945432 Functional Loss SNV dbSNP153 33..33 33 - - - 87186 RMVar_ID_87186 Human_SNP_ID_132379321 m1A Human chr3 - 48932857 48932857 48932857 TTCTACACCACCTTCAAGGTCCTCTGGCCTCAACACAAAGCTCAGGTAGCTCACTACACCTCCTG TTCTACACCACCTTCAAGGTCCTCTGGCCTCAGCACAAAGCTCAGGTAGCTCACTACACCTCCTG T C lnc-NCKIPSD-1 RNACentral:URS00008B560A lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48932844..48932999 26863196 MeRIP-seq:(Medium) rs1383157131 Functional Loss SNV dbSNP153 33..33 33 - - - 87187 RMVar_ID_87187 Human_SNP_ID_132379408 m1A Human chr3 + 48933223 48933223 48933223 AGCCTCCCAAATAGCTGGGACCACAGGTGCGCACCACATGCCCGGGTGTGTGTGTGTGTGTGTGT AGCCTCCCAAATAGCTGGGACCACAGGTGCGCGCCACATGCCCGGGTGTGTGTGTGTGTGTGTGT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48933194..48933334 32194978 MeRIP-seq:(Medium) rs1319731057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5654344,Human_RBP_ID_24007324 RMVar_hsa_circ_218003,RMVar_hsa_circ_112434,RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_328585,RMVar_hsa_circ_316084,RMVar_hsa_circ_52938,RMVar_hsa_circ_305274 87188 RMVar_ID_87188 Human_SNP_ID_132381336 m1A Human chr3 + 48940387 48940383 48940387 AAAAAGATAGATAGATAGATTAGATAGATAAAAAGAGAGAGAGAGAGCGCACAAGTGAGCCAAGT AAAAAGATAGATAGATAGATTAGATAGAT____AGAGAGAGAGAGAGCGCACAAGTGAGCCAAGT TAAAA T ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48940349..48940553 26863196 MeRIP-seq:(Medium) rs1215243665 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_8574494 RMVar_hsa_circ_218003,RMVar_hsa_circ_112434,RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_328585,RMVar_hsa_circ_316084,RMVar_hsa_circ_52938,RMVar_hsa_circ_305274 87189 RMVar_ID_87189 Human_SNP_ID_132381339 m1A Human chr3 + 48940387 48940387 48940387 AAAAAGATAGATAGATAGATTAGATAGATAAAAAGAGAGAGAGAGAGCGCACAAGTGAGCCAAGT AAAAAGATAGATAGATAGATTAGATAGATAAAGAGAGAGAGAGAGAGCGCACAAGTGAGCCAAGT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48940349..48940553 26863196 MeRIP-seq:(Medium) rs996569195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8574494 RMVar_hsa_circ_218003,RMVar_hsa_circ_112434,RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_328585,RMVar_hsa_circ_316084,RMVar_hsa_circ_52938,RMVar_hsa_circ_305274 87190 RMVar_ID_87190 Human_SNP_ID_132389204 m1A Human chr3 + 48970683 48970683 48970683 ACAGGAGCCTAGAGCTCGCCGAGTACAGTGCAATCGGTGCAACGAGGTCTTCTGGTAAGAGTGAG ACAGGAGCCTAGAGCTCGCCGAGTACAGTGCAGTCGGTGCAACGAGGTCTTCTGGTAAGAGTGAG A G ARIH2 Ensembl:ENSG00000177479 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48970617..48970718 32194978 MeRIP-seq:(Medium) rs376123571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_935243,Human_RBP_ID_3965168,Human_RBP_ID_8875009,Human_RBP_ID_9348533,Human_RBP_ID_14862525,Human_RBP_ID_19117419 Human_Splice_Rec_426420,Human_Splice_Rec_426421,Human_Splice_Rec_426446,Human_Splice_Rec_426470,Human_Splice_Rec_426471,Human_Splice_Rec_426494,Human_Splice_Rec_426495,Human_Splice_Rec_426516,Human_Splice_Rec_426517,Human_Splice_Rec_426542,Human_Splice_Rec_426624,Human_Splice_Rec_426625,Human_Splice_Rec_426660,Human_Splice_Rec_426666 RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_99714,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_52938,RMVar_hsa_circ_8152,RMVar_hsa_circ_56438,RMVar_hsa_circ_43608,RMVar_hsa_circ_42850,RMVar_hsa_circ_109511,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_218012 87191 RMVar_ID_87191 Human_SNP_ID_132392038 m1A Human chr3 - 48981698 48981698 48981698 ACCAGCTTCTTCCTGGGTCCGGACTCCATGTAATATGCATATGGGTAGGTGTATTGCAGGGTGTA ACCAGCTTCTTCCTGGGTCCGGACTCCATGTAGTATGCATATGGGTAGGTGTATTGCAGGGTGTA T C AC137630.2 Ensembl:ENSG00000235236 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48979515..48981697 32194978 MeRIP-seq:(Medium) rs1309037363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1137975 87192 RMVar_ID_87192 Human_SNP_ID_132392801 m1A Human chr3 - 48985245 48985245 48985245 TGAGCACAGAAAACCCTCCAGCTCCAGCATCCAGGGCCACAGCTGGACACAAGTACAGAACCTGG TGAGCACAGAAAACCCTCCAGCTCCAGCATCCCGGGCCACAGCTGGACACAAGTACAGAACCTGG T G AC137630.1 Ensembl:ENSG00000223343 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48984838..48985244 32194978 MeRIP-seq:(Medium) rs1022583857 Functional Loss SNV dbSNP153 33..33 33 - - - 87193 RMVar_ID_87193 Human_SNP_ID_132394171 m1A Human chr3 + 48990476 48990476 48990476 TGCTGATGGTGTTCGTGCACCTGTACCTGGGTAACGTGCTGGCGCTGCTGCTCTTCGTGCACTAC TGCTGATGGTGTTCGTGCACCTGTACCTGGGTGACGTGCTGGCGCTGCTGCTCTTCGTGCACTAC A G P4HTM Ensembl:ENSG00000178467 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:48990329..48990515 26863196 MeRIP-seq:(Medium) rs1375495136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3710088,Human_RBP_ID_7204135,Human_RBP_ID_8574556,Human_RBP_ID_18810084 87194 RMVar_ID_87194 Human_SNP_ID_132397989 m1A Human chr3 + 49006761 49006759 49006762 GCCTGGTCACGCGCGGCACCAAGTGGATTGCCAACAACTGGATTAATGTGGACCCCAGCCGAGCG GCCTGGTCACGCGCGGCACCAAGTGGATTGC___CAACTGGATTAATGTGGACCCCAGCCGAGCG CCAA C P4HTM Ensembl:ENSG00000178467 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49006711..49006825 26863196 MeRIP-seq:(Medium) rs778025734 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1628225,Human_RBP_ID_1964402 Human_Splice_Rec_426694,Human_Splice_Rec_426708,Human_Splice_Rec_426714,Human_Splice_Rec_426728,Human_Splice_Rec_426756 87195 RMVar_ID_87195 Human_SNP_ID_132398005 m1A Human chr3 - 49006819 49006819 49006819 AGTCGGTGCCCCCTTCTCGGGCAAGGCGGGCCATCTCCTGTTGGAACAGCGCTTGCCGCGCTCGG AGTCGGTGCCCCCTTCTCGGGCAAGGCGGGCCGTCTCCTGTTGGAACAGCGCTTGCCGCGCTCGG T C lnc-DALRD3-6 RNACentral:URS0000D57F43 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49006801..49006825 32194978 MeRIP-seq:(Medium) rs766371758 Functional Loss SNV dbSNP153 33..33 33 - - - 87196 RMVar_ID_87196 Human_SNP_ID_132398475 m1A Human chr3 - 49007985 49007985 49007985 CCCTCTCCCGGCCCCGCCTTCCCCAAGAGGCCACACCCCCTGAGGGGCCGGGGCCGCCTCCGCCT CCCTCTCCCGGCCCCGCCTTCCCCAAGAGGCCGCACCCCCTGAGGGGCCGGGGCCGCCTCCGCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49007982..49008235 26863196 MeRIP-seq:(Medium) rs1434833231 Functional Loss SNV dbSNP153 33..33 33 - - - 87197 RMVar_ID_87197 Human_SNP_ID_132399754 m1A Human chr3 - 49012201 49012201 49012201 AACGCTTCGGTCTTCTGAAGCTGTAGCCAGCAATCCCTTGCTTTCCAGGTATGACATGCTGAAGA AACGCTTCGGTCTTCTGAAGCTGTAGCCAGCAGTCCCTTGCTTTCCAGGTATGACATGCTGAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49012150..49012940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 87198 RMVar_ID_87198 Human_SNP_ID_132399983 m1A Human chr3 + 49012798 49012798 49012798 CCAATGGGGAAGGTCGTGTCAAGGTTGTCCCCATCAACACTCCAACTGCTGCTGTGGACCAGACC CCAATGGGGAAGGTCGTGTCAAGGTTGTCCCCGTCAACACTCCAACTGCTGCTGTGGACCAGACC A G WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49012747..49012840 26863196 MeRIP-seq:(Medium) rs200956447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1205727,Human_RBP_ID_1628285,Human_RBP_ID_1964428,Human_RBP_ID_3710111,Human_RBP_ID_5150133,Human_RBP_ID_5207333,Human_RBP_ID_5474346,Human_RBP_ID_5530905,Human_RBP_ID_8123519,Human_RBP_ID_8574621,Human_RBP_ID_9435348,Human_RBP_ID_18499678,Human_RBP_ID_18810159,Human_RBP_ID_22093035,Human_RBP_ID_22282422,Human_RBP_ID_22824011,Human_RBP_ID_27319561,Human_RBP_ID_27502689 Human_miRNA_ID_1960170,Human_miRNA_ID_2098374,Human_miRNA_ID_2104321,Human_miRNA_ID_2110275,Human_miRNA_ID_2162820,Human_miRNA_ID_2594036,Human_miRNA_ID_3037586 RMVar_hsa_circ_78740,RMVar_hsa_circ_218022 87199 RMVar_ID_87199 Human_SNP_ID_132400260 m1A Human chr3 + 49013488 49013488 49013488 ACCCTCGGTCACACGAGAAGCTGCACATCGTCAACTGTGGTGGAGGGCACCGTTCGTGGGCATTC ACCCTCGGTCACACGAGAAGCTGCACATCGTCCACTGTGGTGGAGGGCACCGTTCGTGGGCATTC A C WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49013438..49013523 26863196 MeRIP-seq:(Medium) rs751925913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628296,Human_RBP_ID_1964437,Human_RBP_ID_2788974,Human_RBP_ID_3710116,Human_RBP_ID_8872964,Human_RBP_ID_14863238,Human_RBP_ID_18810177,Human_RBP_ID_23023506,Human_RBP_ID_27319571,Human_RBP_ID_27502697 Human_miRNA_ID_2054910 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 87200 RMVar_ID_87200 Human_SNP_ID_132400276 m1A Human chr3 + 49013517 49013517 49013517 GTCAACTGTGGTGGAGGGCACCGTTCGTGGGCATTCTCTGATACTGAGGCGGCCATGGCCTTTGC GTCAACTGTGGTGGAGGGCACCGTTCGTGGGCGTTCTCTGATACTGAGGCGGCCATGGCCTTTGC A G WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49013466..49013680 26863196 MeRIP-seq:(Medium) rs776180698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69263,Human_RBP_ID_836697,Human_RBP_ID_1628296,Human_RBP_ID_1964437,Human_RBP_ID_3720798,Human_RBP_ID_4745661,Human_RBP_ID_5207336,Human_RBP_ID_8872965,Human_RBP_ID_14863238,Human_RBP_ID_22090035,Human_RBP_ID_22282433,Human_RBP_ID_22824023,Human_RBP_ID_27054937 Human_miRNA_ID_1031895,Human_miRNA_ID_1068807,Human_miRNA_ID_2470649,Human_miRNA_ID_2495943,Human_miRNA_ID_2497169 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 87201 RMVar_ID_87201 Human_SNP_ID_132400486 m1A Human chr3 + 49014004 49014004 49014004 GCTTCAGCATCATGGTTACTCCGGACCCCAGCACCCCAAGCCGCCTCGCCTGCCATGTCATGCAC GCTTCAGCATCATGGTTACTCCGGACCCCAGCCCCCCAAGCCGCCTCGCCTGCCATGTCATGCAC A C WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49013954..49014204 26863196 MeRIP-seq:(Medium) rs914842097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247910,Human_RBP_ID_836700,Human_RBP_ID_1628324,Human_RBP_ID_3710121,Human_RBP_ID_7204192,Human_RBP_ID_8574647,Human_RBP_ID_8872978,Human_RBP_ID_9302906,Human_RBP_ID_9435350,Human_RBP_ID_14863266,Human_RBP_ID_18810193,Human_RBP_ID_22090039,Human_RBP_ID_22282441,Human_RBP_ID_22824036,Human_RBP_ID_23023509,Human_RBP_ID_23115936,Human_RBP_ID_26823839,Human_RBP_ID_27054945,Human_RBP_ID_27319577,Human_RBP_ID_27502710 Human_miRNA_ID_1359746,Human_miRNA_ID_2683356 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 87202 RMVar_ID_87202 Human_SNP_ID_132400491 m1A Human chr3 + 49014010 49014010 49014010 GCATCATGGTTACTCCGGACCCCAGCACCCCAAGCCGCCTCGCCTGCCATGTCATGCACCTTTCG GCATCATGGTTACTCCGGACCCCAGCACCCCAGGCCGCCTCGCCTGCCATGTCATGCACCTTTCG A G WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49013821..49014130 26863196 MeRIP-seq:(Medium) rs1233903912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247910,Human_RBP_ID_836700,Human_RBP_ID_3710121,Human_RBP_ID_7204192,Human_RBP_ID_8574647,Human_RBP_ID_9302906,Human_RBP_ID_14863266,Human_RBP_ID_22092370,Human_RBP_ID_23115936,Human_RBP_ID_26823839,Human_RBP_ID_27502710 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 87203 RMVar_ID_87203 Human_SNP_ID_132401076 m1A Human chr3 + 49015439 49015439 49015439 GGTTCCTGATGTCGGTGCAGGAGCTGAAGGTGAGTGGAGTGCTGCCAAGAATATGCCCGACTCCC GGTTCCTGATGTCGGTGCAGGAGCTGAAGGTGCGTGGAGTGCTGCCAAGAATATGCCCGACTCCC A C WDR6 Ensembl:ENSG00000178252 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49015097..49015482 26863196 MeRIP-seq:(Medium) rs925203661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69270,Human_RBP_ID_603932,Human_RBP_ID_1069032,Human_RBP_ID_1628350,Human_RBP_ID_1964458,Human_RBP_ID_3963998,Human_RBP_ID_5120545,Human_RBP_ID_5392969,Human_RBP_ID_5530427,Human_RBP_ID_8574661,Human_RBP_ID_9141403,Human_RBP_ID_14863302,Human_RBP_ID_18169294,Human_RBP_ID_18810224,Human_RBP_ID_19115462,Human_RBP_ID_22092743,Human_RBP_ID_22418254,Human_RBP_ID_24007642 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023,RMVar_hsa_circ_110285,RMVar_hsa_circ_218025 87204 RMVar_ID_87204 Human_SNP_ID_132401090 m1A Human chr3 + 49015476 49015476 49015476 AGTGCTGCCAAGAATATGCCCGACTCCCCATGACAAGACAGAACTTTGTAACAAACAGTACCAAT AGTGCTGCCAAGAATATGCCCGACTCCCCATGGCAAGACAGAACTTTGTAACAAACAGTACCAAT A G WDR6 Ensembl:ENSG00000178252 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49015426..49015525 32194978 MeRIP-seq:(Medium) rs1367575110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628353,Human_RBP_ID_1964458,Human_RBP_ID_2788985,Human_RBP_ID_3710129,Human_RBP_ID_5120263,Human_RBP_ID_14863303,Human_RBP_ID_18810225 Human_miRNA_ID_2837378,Human_miRNA_ID_2855256 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023,RMVar_hsa_circ_110285,RMVar_hsa_circ_218025 87205 RMVar_ID_87205 Human_SNP_ID_132401128 m1A Human chr3 - 49015603 49015603 49015603 CATACTGGCCTGGCTATGCTGGGTCTCCCTCCACTGAGCCACATTTAAGGCCACAGAGGCTCCAA CATACTGGCCTGGCTATGCTGGGTCTCCCTCCGCTGAGCCACATTTAAGGCCACAGAGGCTCCAA T C DALRD3 Ensembl:ENSG00000178149 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49015558..49015880 26863196 MeRIP-seq:(Medium) rs201468616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69256,Human_RBP_ID_603936 RMVar_hsa_circ_120338,RMVar_hsa_circ_218026 87206 RMVar_ID_87206 Human_SNP_ID_132401690 m1A Human chr3 - 49016846 49016846 49016846 CTAGGCTGAGCCCCTGACATCTTTCTGACAGAAGCACCTCATCTGTGGCCCTGTGAAAGTAGCTG CTAGGCTGAGCCCCTGACATCTTTCTGACAGACGCACCTCATCTGTGGCCCTGTGAAAGTAGCTG T G DALRD3 Ensembl:ENSG00000178149 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49016826..49016850 32194978 MeRIP-seq:(Medium) rs1248672463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19012121 Human_Splice_Rec_426916,Human_Splice_Rec_426917,Human_Splice_Rec_426936,Human_Splice_Rec_426937,Human_Splice_Rec_426956,Human_Splice_Rec_426957,Human_Splice_Rec_426970,Human_Splice_Rec_426971,Human_Splice_Rec_426992,Human_Splice_Rec_426993,Human_Splice_Rec_427012,Human_Splice_Rec_427013,Human_Splice_Rec_427036,Human_Splice_Rec_427037,Human_Splice_Rec_427048,Human_Splice_Rec_427049,Human_Splice_Rec_427070 RMVar_hsa_circ_218030,RMVar_hsa_circ_218028,RMVar_hsa_circ_357335,RMVar_hsa_circ_371172,RMVar_hsa_circ_86112,RMVar_hsa_circ_322586,RMVar_hsa_circ_218029 87207 RMVar_ID_87207 Human_SNP_ID_132401972 m1A Human chr3 + 49017604 49017604 49017604 CCCTCCTGCCTTTTCTGGCCCTGCTAGGCTTCAGGTCCTACCCAGACAGTTGTCCAGGTTGGGGT CCCTCCTGCCTTTTCTGGCCCTGCTAGGCTTCGGGTCCTACCCAGACAGTTGTCCAGGTTGGGGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49017601..49017650 32194978 MeRIP-seq:(Medium) rs1362559563 Functional Loss SNV dbSNP153 33..33 33 - - - 87208 RMVar_ID_87208 Human_SNP_ID_132402014 m1A Human chr3 - 49017723 49017723 49017723 GAGCCACGCCCTTGAAGAACTTACCTCTGCTAATGACGGGAGGACACTGTCCCCTGGCATCCTAG GAGCCACGCCCTTGAAGAACTTACCTCTGCTAGTGACGGGAGGACACTGTCCCCTGGCATCCTAG T C DALRD3 Ensembl:ENSG00000178149 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49017674..49017802 26863196 MeRIP-seq:(Medium) rs761345101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246912 RMVar_hsa_circ_218030,RMVar_hsa_circ_86112 87209 RMVar_ID_87209 Human_SNP_ID_132402232 m1A Human chr3 + 49018201 49018201 49018201 ATAGGCGGCCACGGCGCTGAGGACGCGCTCGAAGACGGCGGACCGCTGCAGTTGGAGAGACAGAC ATAGGCGGCCACGGCGCTGAGGACGCGCTCGAGGACGGCGGACCGCTGCAGTTGGAGAGACAGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49018151..49018250 32194978 MeRIP-seq:(Medium) rs1339446414 Functional Loss SNV dbSNP153 33..33 33 - - - 87210 RMVar_ID_87210 Human_SNP_ID_132402409 m1A Human chr3 + 49018530 49018530 49018530 CGCCTGGCCCCAGGGCCGCGTTGAGGGCCCCCAGCGTCTCCCCGACCCCAAGGCGCCTGGTCGCC CGCCTGGCCCCAGGGCCGCGTTGAGGGCCCCCCGCGTCTCCCCGACCCCAAGGCGCCTGGTCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49018401..49018575 26863196 MeRIP-seq:(Medium) rs947421816 Functional Loss SNV dbSNP153 33..33 33 - - - 87211 RMVar_ID_87211 Human_SNP_ID_132402410 m1A Human chr3 + 49018530 49018530 49018530 CGCCTGGCCCCAGGGCCGCGTTGAGGGCCCCCAGCGTCTCCCCGACCCCAAGGCGCCTGGTCGCC CGCCTGGCCCCAGGGCCGCGTTGAGGGCCCCCGGCGTCTCCCCGACCCCAAGGCGCCTGGTCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49018401..49018575 26863196 MeRIP-seq:(Medium) rs947421816 Functional Loss SNV dbSNP153 33..33 33 - - - 87212 RMVar_ID_87212 Human_SNP_ID_132403538 m1A Human chr3 - 49022146 49022146 49022146 GGTACAAGCTACGTAGCGCGAGAGCGGTGGCCATGGCTGACCAACGCGCGGCGAAGTCGTCACCG GGTACAAGCTACGTAGCGCGAGAGCGGTGGCCGTGGCTGACCAACGCGCGGCGAAGTCGTCACCG T C DALRD3 Ensembl:ENSG00000178149 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49021742..49022200 26863196 MeRIP-seq:(Medium) rs121918136 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_471 87213 RMVar_ID_87213 Human_SNP_ID_132403539 m1A Human chr3 - 49022146 49022146 49022146 GGTACAAGCTACGTAGCGCGAGAGCGGTGGCCATGGCTGACCAACGCGCGGCGAAGTCGTCACCG GGTACAAGCTACGTAGCGCGAGAGCGGTGGCCCTGGCTGACCAACGCGCGGCGAAGTCGTCACCG T G DALRD3 Ensembl:ENSG00000178149 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49021742..49022200 26863196 MeRIP-seq:(Medium) rs121918136 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_471 87214 RMVar_ID_87214 Human_SNP_ID_132403699 m1A Human chr3 + 49022435 49022435 49022435 GCGCATCTCTCTGCTGCAACGCGAGGCCGCTCAGGCAATGTACATCGACAGCTACAACAGCCGCG GCGCATCTCTCTGCTGCAACGCGAGGCCGCTCTGGCAATGTACATCGACAGCTACAACAGCCGCG A T NDUFAF3 Ensembl:ENSG00000178057 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49022385..49022550 26863196 MeRIP-seq:(Medium) rs1468909521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22768611 Human_Splice_Rec_427076,Human_Splice_Rec_427084,Human_Splice_Rec_427092,Human_Splice_Rec_427106,Human_Splice_Rec_427110 Human_miRNA_ID_2728983 RMVar_hsa_circ_95686,RMVar_hsa_circ_218031 87215 RMVar_ID_87215 Human_SNP_ID_132403752 m1A Human chr3 + 49022531 49022531 49022531 CCCCTGCGCTCTGCTCCCGCACTCGGTGGTGCAGTGGAACGTGAGTCCTGGCCCGCAGTGTGGAA CCCCTGCGCTCTGCTCCCGCACTCGGTGGTGCGGTGGAACGTGAGTCCTGGCCCGCAGTGTGGAA A G NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49021792..49022800 32194978 MeRIP-seq:(Medium) rs1490281636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603961,Human_RBP_ID_24007654 Human_Splice_Rec_427077,Human_Splice_Rec_427085,Human_Splice_Rec_427093,Human_Splice_Rec_427099,Human_Splice_Rec_427107,Human_Splice_Rec_427111 Human_miRNA_ID_2967728 RMVar_hsa_circ_95686,RMVar_hsa_circ_218031 87216 RMVar_ID_87216 Human_SNP_ID_132403853 m1A Human chr3 + 49022757 49022757 49022757 CGAAGACAGCTTTTCCCTCTTCTGGTTGCTGGAGCCCCGGATAGGTACTGGGGAAGGGGAGGGAG CGAAGACAGCTTTTCCCTCTTCTGGTTGCTGGCGCCCCGGATAGGTACTGGGGAAGGGGAGGGAG A C NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:49022101..49022775 26863196 MeRIP-seq:(Medium) rs1428089867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603962,Human_RBP_ID_18446709,Human_RBP_ID_19012124,Human_RBP_ID_22824064,Human_RBP_ID_27841414 Human_Splice_Rec_427078,Human_Splice_Rec_427079,Human_Splice_Rec_427086,Human_Splice_Rec_427087,Human_Splice_Rec_427094,Human_Splice_Rec_427095,Human_Splice_Rec_427100,Human_Splice_Rec_427101,Human_Splice_Rec_427108,Human_Splice_Rec_427112,Human_Splice_Rec_427113 RMVar_hsa_circ_95686,RMVar_hsa_circ_218031 87217 RMVar_ID_87217 Human_SNP_ID_132403859 m1A Human chr3 + 49022765 49022765 49022765 GCTTTTCCCTCTTCTGGTTGCTGGAGCCCCGGATAGGTACTGGGGAAGGGGAGGGAGAACAGAGG GCTTTTCCCTCTTCTGGTTGCTGGAGCCCCGGTTAGGTACTGGGGAAGGGGAGGGAGAACAGAGG A T NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49022288..49022800 26863196 MeRIP-seq:(Medium) rs775271762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603964,Human_RBP_ID_19012124,Human_RBP_ID_22824064,Human_RBP_ID_24561350,Human_RBP_ID_27841414 Human_Splice_Rec_427078,Human_Splice_Rec_427079,Human_Splice_Rec_427086,Human_Splice_Rec_427087,Human_Splice_Rec_427094,Human_Splice_Rec_427095,Human_Splice_Rec_427100,Human_Splice_Rec_427101,Human_Splice_Rec_427108,Human_Splice_Rec_427112,Human_Splice_Rec_427113 RMVar_hsa_circ_95686,RMVar_hsa_circ_218031 87218 RMVar_ID_87218 Human_SNP_ID_132403914 m1A Human chr3 + 49022876 49022876 49022876 ACTGTAGACTAGCCACACCCACCCTTCCCTAGAGATCGTGGTGGTGGGGACTGGAGACCGGACCG ACTGTAGACTAGCCACACCCACCCTTCCCTAGGGATCGTGGTGGTGGGGACTGGAGACCGGACCG A G NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1466360477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248613,Human_RBP_ID_603966,Human_RBP_ID_17704237,Human_RBP_ID_19010278,Human_RBP_ID_19115464 Human_Splice_Rec_427080,Human_Splice_Rec_427088,Human_Splice_Rec_427096,Human_Splice_Rec_427102,Human_Splice_Rec_427114 87219 RMVar_ID_87219 Human_SNP_ID_132404037 m1A Human chr3 + 49023168 49023168 49023168 GACTTCACTTACATCTTTGGGCCAAGCTGCTCAATGAACCGCCAGGAACTGACCTGCTGACTGCA GACTTCACTTACATCTTTGGGCCAAGCTGCTCGATGAACCGCCAGGAACTGACCTGCTGACTGCA A G NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49023117..49023207 26863196 MeRIP-seq:(Medium) rs886058668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603975,Human_RBP_ID_935257,Human_RBP_ID_1628376,Human_RBP_ID_1964468,Human_RBP_ID_9141411,Human_RBP_ID_9395000,Human_RBP_ID_14863353,Human_RBP_ID_17292037,Human_RBP_ID_17404942,Human_RBP_ID_17661393,Human_RBP_ID_18007176,Human_RBP_ID_24007656,Human_RBP_ID_26512111 Clinvar_Rec_472 87220 RMVar_ID_87220 Human_SNP_ID_132404644 m1A Human chr3 + 49024958 49024958 49024958 TTGTCCATGGCATCGAGAGAACCCATACCGCGATATTTCTTTAGCCGGATCCCATCGGAAAAGAA TTGTCCATGGCATCGAGAGAACCCATACCGCGGTATTTCTTTAGCCGGATCCCATCGGAAAAGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49024874..49024992 26863196 MeRIP-seq:(Medium) rs72553873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8574690 Clinvar_Rec_473 87221 RMVar_ID_87221 Human_SNP_ID_132404653 m1A Human chr3 + 49024990 49024990 49024990 ATATTTCTTTAGCCGGATCCCATCGGAAAAGAAGTATTCACCAGGGGCCTCAGTGGTGGCAGCCA ATATTTCTTTAGCCGGATCCCATCGGAAAAGACGTATTCACCAGGGGCCTCAGTGGTGGCAGCCA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49024876..49025050 32194978 MeRIP-seq:(Medium) rs866481725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628390,Human_RBP_ID_8574690,Human_RBP_ID_14863458 87222 RMVar_ID_87222 Human_SNP_ID_132404654 m1A Human chr3 + 49024990 49024990 49024990 ATATTTCTTTAGCCGGATCCCATCGGAAAAGAAGTATTCACCAGGGGCCTCAGTGGTGGCAGCCA ATATTTCTTTAGCCGGATCCCATCGGAAAAGATGTATTCACCAGGGGCCTCAGTGGTGGCAGCCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49024876..49025050 32194978 MeRIP-seq:(Medium) rs866481725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628390,Human_RBP_ID_8574690,Human_RBP_ID_14863458 87223 RMVar_ID_87223 Human_SNP_ID_132404742 m1A Human chr3 + 49025261 49025261 49025261 CTTGTACACTGCTGTTGCTTGGGGCCGCCCACAGGCCAGCACTGTTGAGATGGAGGAACACATGG CTTGTACACTGCTGTTGCTTGGGGCCGCCCACGGGCCAGCACTGTTGAGATGGAGGAACACATGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49025126..49025275 32194978 MeRIP-seq:(Medium) rs1173661177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604017,Human_RBP_ID_14863473,Human_RBP_ID_20786788 87224 RMVar_ID_87224 Human_SNP_ID_132405089 m1A Human chr3 + 49026309 49026309 49026309 GGCCTGAAACTGGGGTCTCTGTGGGCCCTATCAAAGTATATTCTTACCTTCCTGCGTAATGCAGA GGCCTGAAACTGGGGTCTCTGTGGGCCCTATCCAAGTATATTCTTACCTTCCTGCGTAATGCAGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49026301..49026350 26863196 MeRIP-seq:(Medium) rs747105993 Functional Loss SNV dbSNP153 33..33 33 - - - 87225 RMVar_ID_87225 Human_SNP_ID_132405090 m1A Human chr3 + 49026309 49026309 49026309 GGCCTGAAACTGGGGTCTCTGTGGGCCCTATCAAAGTATATTCTTACCTTCCTGCGTAATGCAGA GGCCTGAAACTGGGGTCTCTGTGGGCCCTATCGAAGTATATTCTTACCTTCCTGCGTAATGCAGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49026301..49026350 26863196 MeRIP-seq:(Medium) rs747105993 Functional Loss SNV dbSNP153 33..33 33 - - - 87226 RMVar_ID_87226 Human_SNP_ID_132405115 m1A Human chr3 - 49026374 49026374 49026374 CCAGGCCAAGAACCTCATTGATGCAGGTGTGGATGCCCTGCGGGTGGGCATGGGAAGTGGCTCCA CCAGGCCAAGAACCTCATTGATGCAGGTGTGGGTGCCCTGCGGGTGGGCATGGGAAGTGGCTCCA T C IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr3:49026292..49026429;chr3:49026301..49026425 26863196 MeRIP-seq:(Medium) rs752303460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69236,Human_RBP_ID_604020,Human_RBP_ID_1628395,Human_RBP_ID_5392975,Human_RBP_ID_8574696,Human_RBP_ID_8873020,Human_RBP_ID_9261133,Human_RBP_ID_9302320,Human_RBP_ID_9354321,Human_RBP_ID_17704241,Human_RBP_ID_18007195,Human_RBP_ID_22426544,Human_RBP_ID_22455433,Human_RBP_ID_22824085,Human_RBP_ID_24007672 Human_Splice_Rec_427136,Human_Splice_Rec_427137,Human_Splice_Rec_427164,Human_Splice_Rec_427165,Human_Splice_Rec_427192 Human_miRNA_ID_2695173 RMVar_hsa_circ_93264,RMVar_hsa_circ_113558,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218036,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_64720,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_371174,RMVar_hsa_circ_94815,RMVar_hsa_circ_26823,RMVar_hsa_circ_218039,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_218040 87227 RMVar_ID_87227 Human_SNP_ID_132405116 m1A Human chr3 + 49026377 49026377 49026377 AGCCACTTCCCATGCCCACCCGCAGGGCATCCACACCTGCATCAATGAGGTTCTTGGCCTGGGCA AGCCACTTCCCATGCCCACCCGCAGGGCATCCCCACCTGCATCAATGAGGTTCTTGGCCTGGGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:49026301..49026425;chr3:49026301..49026575 26863196 MeRIP-seq:(Medium) rs755742896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18810271 87228 RMVar_ID_87228 Human_SNP_ID_132405160 m1A Human chr3 + 49026504 49026504 49026504 CTTACCCACTCCCACCACACATCCTTCAGGGCACAATCTTGCCTTACCATTGCCTCCAATGACTT CTTACCCACTCCCACCACACATCCTTCAGGGCCCAATCTTGCCTTACCATTGCCTCCAATGACTT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49026501..49026525 32194978 MeRIP-seq:(Medium) rs374744612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18810272 87229 RMVar_ID_87229 Human_SNP_ID_132405161 m1A Human chr3 + 49026506 49026506 49026506 TACCCACTCCCACCACACATCCTTCAGGGCACAATCTTGCCTTACCATTGCCTCCAATGACTTGG TACCCACTCCCACCACACATCCTTCAGGGCACCATCTTGCCTTACCATTGCCTCCAATGACTTGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49026501..49026550 26863196 MeRIP-seq:(Medium) rs753419653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18810272 87230 RMVar_ID_87230 Human_SNP_ID_132405185 m1A Human chr3 - 49026576 49026576 49026576 ACTCTTCCCAGGGAAATTCCATCTTCCAGATCAATATGATCAAGTACATCAAAGACAAATACCCT ACTCTTCCCAGGGAAATTCCATCTTCCAGATCGATATGATCAAGTACATCAAAGACAAATACCCT T C IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49026551..49026575 32194978 MeRIP-seq:(Medium) rs368925413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69237,Human_RBP_ID_604024,Human_RBP_ID_933744,Human_RBP_ID_1033593,Human_RBP_ID_1964481,Human_RBP_ID_2789006,Human_RBP_ID_3965175,Human_RBP_ID_5390761,Human_RBP_ID_8873021,Human_RBP_ID_18535986,Human_RBP_ID_22456608 Human_Splice_Rec_427134,Human_Splice_Rec_427135,Human_Splice_Rec_427162,Human_Splice_Rec_427163,Human_Splice_Rec_427190,Human_Splice_Rec_427191,Human_Splice_Rec_427204,Human_Splice_Rec_427208 RMVar_hsa_circ_93264,RMVar_hsa_circ_113558,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218036,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_64720,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_371174,RMVar_hsa_circ_94815,RMVar_hsa_circ_26823,RMVar_hsa_circ_218039,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_218040,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043 87231 RMVar_ID_87231 Human_SNP_ID_132405190 m1A Human chr3 - 49026595 49026595 49026595 ACTTACTTCTTGTCCTAGGACTCTTCCCAGGGAAATTCCATCTTCCAGATCAATATGATCAAGTA ACTTACTTCTTGTCCTAGGACTCTTCCCAGGGCAATTCCATCTTCCAGATCAATATGATCAAGTA T G IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49026501..49027925 32194978 MeRIP-seq:(Medium) rs1168426638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69237,Human_RBP_ID_604024,Human_RBP_ID_933744,Human_RBP_ID_1033593,Human_RBP_ID_1069172,Human_RBP_ID_2789007,Human_RBP_ID_3965175,Human_RBP_ID_5390761,Human_RBP_ID_8873021,Human_RBP_ID_19120549,Human_RBP_ID_22456608,Human_RBP_ID_22745179 Human_Splice_Rec_427134,Human_Splice_Rec_427135,Human_Splice_Rec_427162,Human_Splice_Rec_427163,Human_Splice_Rec_427190,Human_Splice_Rec_427191,Human_Splice_Rec_427204,Human_Splice_Rec_427208 RMVar_hsa_circ_93264,RMVar_hsa_circ_113558,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218036,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_64720,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_371174,RMVar_hsa_circ_94815,RMVar_hsa_circ_26823,RMVar_hsa_circ_218039,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_218040,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043 87232 RMVar_ID_87232 Human_SNP_ID_132405238 m1A Human chr3 - 49026736 49026736 49026736 TGGGGCAGCCATTGGCACTCATGAGGATGACAAGTATAGGCTGGACTTGCTCGCCCAGGCTGGTG TGGGGCAGCCATTGGCACTCATGAGGATGACAGGTATAGGCTGGACTTGCTCGCCCAGGCTGGTG T C IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49026608..49027065 26863196 MeRIP-seq:(Medium) rs1219770046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604025,Human_RBP_ID_9302909,Human_RBP_ID_14863536,Human_RBP_ID_18169439,Human_RBP_ID_24007674 Human_Splice_Rec_427133,Human_Splice_Rec_427161,Human_Splice_Rec_427189,Human_Splice_Rec_427203,Human_Splice_Rec_427207 Human_miRNA_ID_2972614,Human_miRNA_ID_3005800 RMVar_hsa_circ_93264,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_64720,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_94815,RMVar_hsa_circ_26823,RMVar_hsa_circ_76880,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_218040,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043,RMVar_hsa_circ_218044,RMVar_hsa_circ_8095 87233 RMVar_ID_87233 Human_SNP_ID_132405819 m1A Human chr3 - 49028531 49028531 49028531 TTCCCACACTGGTTGACGTTTGTCTCCTCAGGACCTGACTTCTGCTCTGACCAAGAAAATCACTC TTCCCACACTGGTTGACGTTTGTCTCCTCAGGCCCTGACTTCTGCTCTGACCAAGAAAATCACTC T G IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49028226..49028566 32194978 MeRIP-seq:(Medium) rs977987012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247897,Human_RBP_ID_604049,Human_RBP_ID_784153,Human_RBP_ID_1033601,Human_RBP_ID_1313220,Human_RBP_ID_4765994,Human_RBP_ID_14863645,Human_RBP_ID_17291399,Human_RBP_ID_17404617,Human_RBP_ID_17521549,Human_RBP_ID_19010279,Human_RBP_ID_22551522,Human_RBP_ID_22824104 Human_Splice_Rec_427152,Human_Splice_Rec_427196,Human_Splice_Rec_427218 Human_miRNA_ID_2251201 RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218032,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_87805,RMVar_hsa_circ_76880,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043,RMVar_hsa_circ_50188,RMVar_hsa_circ_218044,RMVar_hsa_circ_331915,RMVar_hsa_circ_18783,RMVar_hsa_circ_114432,RMVar_hsa_circ_218047,RMVar_hsa_circ_218048,RMVar_hsa_circ_218046 87234 RMVar_ID_87234 Human_SNP_ID_132405888 m1A Human chr3 - 49028754 49028754 49028754 GGTACATCGACTTCACTGCAGACCAGGTGGTGAGTATGATCAGGAATTGGGTCCTGAACATCAAG GGTACATCGACTTCACTGCAGACCAGGTGGTGGGTATGATCAGGAATTGGGTCCTGAACATCAAG T C IMPDH2 Ensembl:ENSG00000178035 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49028751..49028825 32194978 MeRIP-seq:(Medium) rs1226719417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19012130,Human_RBP_ID_19117441,Human_RBP_ID_22824107,Human_RBP_ID_26346285 Human_Splice_Rec_427150,Human_Splice_Rec_427194,Human_Splice_Rec_427210,Human_Splice_Rec_427216 RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218032,RMVar_hsa_circ_108727,RMVar_hsa_circ_87805,RMVar_hsa_circ_76880,RMVar_hsa_circ_218042,RMVar_hsa_circ_218044,RMVar_hsa_circ_18783,RMVar_hsa_circ_114432,RMVar_hsa_circ_218047,RMVar_hsa_circ_218048 87235 RMVar_ID_87235 Human_SNP_ID_132406157 m1A Human chr3 + 49029360 49029360 49029360 CCACTAATCAGGTAGTCGGCCATGGCCAACACAGGACACCGCCGCGTGTCTCCGAGGACCGCGCC CCACTAATCAGGTAGTCGGCCATGGCCAACACCGGACACCGCCGCGTGTCTCCGAGGACCGCGCC A C AC137630.3 Ensembl:ENSG00000272434 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49029182..49029400 26863196 MeRIP-seq:(Medium) rs533465405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3172934 87236 RMVar_ID_87236 Human_SNP_ID_132406158 m1A Human chr3 + 49029360 49029360 49029360 CCACTAATCAGGTAGTCGGCCATGGCCAACACAGGACACCGCCGCGTGTCTCCGAGGACCGCGCC CCACTAATCAGGTAGTCGGCCATGGCCAACACGGGACACCGCCGCGTGTCTCCGAGGACCGCGCC A G AC137630.3 Ensembl:ENSG00000272434 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49029182..49029400 26863196 MeRIP-seq:(Medium) rs533465405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3172934 87237 RMVar_ID_87237 Human_SNP_ID_132414367 m1A Human chr3 + 49057737 49057737 49057737 TTGCAGCTGCGAGGGACTGGGACTCTGCAGAGACGGGGTCTGAATGGAGGGGGCTGCTGACTGTG TTGCAGCTGCGAGGGACTGGGACTCTGCAGAGCCGGGGTCTGAATGGAGGGGGCTGCTGACTGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:49057690..49057875;chr3:49057691..49057824 26863196 MeRIP-seq:(Medium) rs746921683 Functional Loss SNV dbSNP153 33..33 33 - - - 87238 RMVar_ID_87238 Human_SNP_ID_132414379 m1A Human chr3 - 49057766 49057766 49057766 GGTCCAGGTGCAGATCCAAGGCCAGGCACCACAGTCAGCAGCCCCCTCCATTCAGACCCCGTCTC GGTCCAGGTGCAGATCCAAGGCCAGGCACCACTGTCAGCAGCCCCCTCCATTCAGACCCCGTCTC T A QRICH1 Ensembl:ENSG00000198218 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49057627..49057900 26863196 MeRIP-seq:(Medium) rs1488328138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1313230,Human_RBP_ID_17404624 Human_miRNA_ID_2948524 RMVar_hsa_circ_10931,RMVar_hsa_circ_54028,RMVar_hsa_circ_308831,RMVar_hsa_circ_316508,RMVar_hsa_circ_218053,RMVar_hsa_circ_218054,RMVar_hsa_circ_71815,RMVar_hsa_circ_336678,RMVar_hsa_circ_308718,RMVar_hsa_circ_310788,RMVar_hsa_circ_218059,RMVar_hsa_circ_218057,RMVar_hsa_circ_218058,RMVar_hsa_circ_218060 87239 RMVar_ID_87239 Human_SNP_ID_132414381 m1A Human chr3 - 49057771 49057771 49057771 ATCCAGGTCCAGGTGCAGATCCAAGGCCAGGCACCACAGTCAGCAGCCCCCTCCATTCAGACCCC ATCCAGGTCCAGGTGCAGATCCAAGGCCAGGCGCCACAGTCAGCAGCCCCCTCCATTCAGACCCC T C QRICH1 Ensembl:ENSG00000198218 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:49057695..49057862 26863196 MeRIP-seq:(Medium) rs761287050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1313230,Human_RBP_ID_17404624 Human_miRNA_ID_2948524 RMVar_hsa_circ_10931,RMVar_hsa_circ_54028,RMVar_hsa_circ_308831,RMVar_hsa_circ_316508,RMVar_hsa_circ_218053,RMVar_hsa_circ_218054,RMVar_hsa_circ_71815,RMVar_hsa_circ_336678,RMVar_hsa_circ_308718,RMVar_hsa_circ_310788,RMVar_hsa_circ_218059,RMVar_hsa_circ_218057,RMVar_hsa_circ_218058,RMVar_hsa_circ_218060 87240 RMVar_ID_87240 Human_SNP_ID_132414389 m1A Human chr3 - 49057799 49057799 49057799 CACCGTTCACCAGCCTACTGAGCAACCCATCCAGGTCCAGGTGCAGATCCAAGGCCAGGCACCAC CACCGTTCACCAGCCTACTGAGCAACCCATCCGGGTCCAGGTGCAGATCCAAGGCCAGGCACCAC T C QRICH1 Ensembl:ENSG00000198218 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49057776..49057800 26863196 MeRIP-seq:(Medium) rs1420370590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17404624,Human_RBP_ID_27055149 Human_Splice_Rec_427224,Human_Splice_Rec_427246,Human_Splice_Rec_427266,Human_Splice_Rec_427297 Human_miRNA_ID_2508716,Human_miRNA_ID_2750139 RMVar_hsa_circ_10931,RMVar_hsa_circ_54028,RMVar_hsa_circ_308831,RMVar_hsa_circ_316508,RMVar_hsa_circ_218053,RMVar_hsa_circ_218054,RMVar_hsa_circ_71815,RMVar_hsa_circ_336678,RMVar_hsa_circ_308718,RMVar_hsa_circ_310788,RMVar_hsa_circ_218057,RMVar_hsa_circ_218058,RMVar_hsa_circ_218060 87241 RMVar_ID_87241 Human_SNP_ID_132419818 m1A Human chr3 - 49076675 49076675 49076675 TATATGGGAAATGCTGAGGTGCAGCCTGTTTAATGTACTTTATTTGTTGTCAGTGTTTTAGTTAG TATATGGGAAATGCTGAGGTGCAGCCTGTTTAGTGTACTTTATTTGTTGTCAGTGTTTTAGTTAG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49076672..49076831 26863196 MeRIP-seq:(Medium) rs1320776668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931,RMVar_hsa_circ_54028,RMVar_hsa_circ_308831,RMVar_hsa_circ_218053,RMVar_hsa_circ_71815,RMVar_hsa_circ_336678,RMVar_hsa_circ_308718,RMVar_hsa_circ_218058 87242 RMVar_ID_87242 Human_SNP_ID_132424931 m1A Human chr3 + 49093952 49093944 49093953 GTCACTGCCGCCGCCGCCGCCGCCTCCGCTGCACCCGCCGGCCCCGCCGCACCGCCAGGGACCCT GTCACTGCCGCCGCCGCCGCCGCCT_________CCGCCGGCCCCGCCGCACCGCCAGGGACCCT TCCGCTGCAC T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49093912..49094063 32194978 MeRIP-seq:(Medium) rs1173832067 Functional Loss DEL dbSNP153 26..34 33 - - - 87243 RMVar_ID_87243 Human_SNP_ID_132424935 m1A Human chr3 + 49093952 49093952 49093952 GTCACTGCCGCCGCCGCCGCCGCCTCCGCTGCACCCGCCGGCCCCGCCGCACCGCCAGGGACCCT GTCACTGCCGCCGCCGCCGCCGCCTCCGCTGCCCCCGCCGGCCCCGCCGCACCGCCAGGGACCCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49093912..49094063 32194978 MeRIP-seq:(Medium) rs918638543 Functional Loss SNV dbSNP153 33..33 33 - - - 87244 RMVar_ID_87244 Human_SNP_ID_132424961 m1A Human chr3 + 49094014 49094014 49094014 CCTGGTTCTGCCGTCGTCGCTCCAAGACCGACAGGGTTTTCTCCTCACAGCTCCCTGGGCGCCAT CCTGGTTCTGCCGTCGTCGCTCCAAGACCGACGGGGTTTTCTCCTCACAGCTCCCTGGGCGCCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49093847..49094213 26863196 MeRIP-seq:(Medium) rs1559962444 Functional Loss SNV dbSNP153 33..33 33 - - - 87245 RMVar_ID_87245 Human_SNP_ID_132424964 m1A Human chr3 - 49094018 49094018 49094018 TAAGATGGCGCCCAGGGAGCTGTGAGGAGAAAACCCTGTCGGTCTTGGAGCGACGACGGCAGAAC TAAGATGGCGCCCAGGGAGCTGTGAGGAGAAAGCCCTGTCGGTCTTGGAGCGACGACGGCAGAAC T C QRICH1 Ensembl:ENSG00000198218 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:49093775..49094075 26863196 MeRIP-seq:(Medium) rs1251085311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1313235,Human_RBP_ID_4758799,Human_RBP_ID_14865082,Human_RBP_ID_18810341,Human_RBP_ID_23026508 87246 RMVar_ID_87246 Human_SNP_ID_132426267 m1A Human chr3 - 49098196 49098196 49098196 TGAGGTGCCTGGTGGATTTTTAAGTGACCTGAACCTGGTAGGTTCATGAGGTTTGGGGTGAGGGA TGAGGTGCCTGGTGGATTTTTAAGTGACCTGAGCCTGGTAGGTTCATGAGGTTTGGGGTGAGGGA T C QARS1 Ensembl:ENSG00000172053 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs373642539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18013313,Human_RBP_ID_23213141,Human_RBP_ID_26823852 Human_Splice_Rec_427327,Human_Splice_Rec_427342,Human_Splice_Rec_427343,Human_Splice_Rec_427362,Human_Splice_Rec_427363,Human_Splice_Rec_427408,Human_Splice_Rec_427409,Human_Splice_Rec_427418,Human_Splice_Rec_427419,Human_Splice_Rec_427460,Human_Splice_Rec_427461,Human_Splice_Rec_427506,Human_Splice_Rec_427507,Human_Splice_Rec_427512,Human_Splice_Rec_427513,Human_Splice_Rec_427524,Human_Splice_Rec_427525,Human_Splice_Rec_427570,Human_Splice_Rec_427571,Human_Splice_Rec_427620,Human_Splice_Rec_427621,Human_Splice_Rec_427640,Human_Splice_Rec_427641,Human_Splice_Rec_427694,Human_Splice_Rec_427695,Human_Splice_Rec_427748,Human_Splice_Rec_427749,Human_Splice_Rec_427760,Human_Splice_Rec_427761 RMVar_hsa_circ_19993,RMVar_hsa_circ_97052,RMVar_hsa_circ_113013,RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_218064,RMVar_hsa_circ_80230,RMVar_hsa_circ_80291,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_218065,RMVar_hsa_circ_218062,RMVar_hsa_circ_218063 87247 RMVar_ID_87247 Human_SNP_ID_132426679 m1A Human chr3 + 49099122 49099122 49099122 ACATGTTGAGGCAGGCCCACCTTGGCAGCAGGAAAGTTGGTGATGATGACCCGTAGTGACTCCAG ACATGTTGAGGCAGGCCCACCTTGGCAGCAGGGAAGTTGGTGATGATGACCCGTAGTGACTCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49099109..49099246 26863196 MeRIP-seq:(Medium) rs762223639 Functional Loss SNV dbSNP153 33..33 33 - - - 87248 RMVar_ID_87248 Human_SNP_ID_132426878 m1A Human chr3 - 49099622 49099622 49099622 ACCCCAGACGCTCTTCCTACTTCTGGCTTTGCAATGCACTGGACGTCTATTGCCCTGTGCAGTGG ACCCCAGACGCTCTTCCTACTTCTGGCTTTGCGATGCACTGGACGTCTATTGCCCTGTGCAGTGG T C QARS1 Ensembl:ENSG00000172053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49099573..49099648 26863196 MeRIP-seq:(Medium) rs941153059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604104 Human_Splice_Rec_427350,Human_Splice_Rec_427396,Human_Splice_Rec_427448,Human_Splice_Rec_427494,Human_Splice_Rec_427558,Human_Splice_Rec_427608,Human_Splice_Rec_427628,Human_Splice_Rec_427682,Human_Splice_Rec_427736,Human_Splice_Rec_427770,Human_Splice_Rec_427778,Human_Splice_Rec_427788 Human_miRNA_ID_332617,Human_miRNA_ID_349682,Human_miRNA_ID_1195557,Human_miRNA_ID_2077901,Human_miRNA_ID_2080229,Human_miRNA_ID_2090766,Human_miRNA_ID_2444993,Human_miRNA_ID_2446379 RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_218064,RMVar_hsa_circ_80230,RMVar_hsa_circ_80291,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_218065,RMVar_hsa_circ_78406,RMVar_hsa_circ_218068,RMVar_hsa_circ_51937 87249 RMVar_ID_87249 Human_SNP_ID_132426880 m1A Human chr3 + 49099627 49099627 49099627 GCACAGGGCAATAGACGTCCAGTGCATTGCAAAGCCAGAAGTAGGAAGAGCGTCTGGGGTGGGAG GCACAGGGCAATAGACGTCCAGTGCATTGCAAGGCCAGAAGTAGGAAGAGCGTCTGGGGTGGGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49099501..49099650 32194978 MeRIP-seq:(Medium) rs1559967291 Functional Loss SNV dbSNP153 33..33 33 - - - 87250 RMVar_ID_87250 Human_SNP_ID_132427070 m1A Human chr3 - 49100043 49100043 49100043 AGTTTTCAGAGGGCGAGGCCACACTACGGATGAAGCTGGTGATGGAGGATGGCAAGATGGACCCT AGTTTTCAGAGGGCGAGGCCACACTACGGATGTAGCTGGTGATGGAGGATGGCAAGATGGACCCT T A QARS1 Ensembl:ENSG00000172053 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49099951..49100050 32194978 MeRIP-seq:(Medium) rs907202044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836192,Human_RBP_ID_938601,Human_RBP_ID_1205772,Human_RBP_ID_1964558,Human_RBP_ID_3964003,Human_RBP_ID_7204538,Human_RBP_ID_9302321,Human_RBP_ID_18194843,Human_RBP_ID_18810358,Human_RBP_ID_19012142,Human_RBP_ID_19115481,Human_RBP_ID_22457329,Human_RBP_ID_22824140,Human_RBP_ID_24007749,Human_RBP_ID_26346286,Human_RBP_ID_26790300,Human_RBP_ID_26824707,Human_RBP_ID_27055183 Human_Splice_Rec_427346,Human_Splice_Rec_427347,Human_Splice_Rec_427392,Human_Splice_Rec_427393,Human_Splice_Rec_427444,Human_Splice_Rec_427445,Human_Splice_Rec_427490,Human_Splice_Rec_427491,Human_Splice_Rec_427554,Human_Splice_Rec_427555,Human_Splice_Rec_427604,Human_Splice_Rec_427605,Human_Splice_Rec_427625,Human_Splice_Rec_427678,Human_Splice_Rec_427679,Human_Splice_Rec_427732,Human_Splice_Rec_427733,Human_Splice_Rec_427766,Human_Splice_Rec_427767,Human_Splice_Rec_427775,Human_Splice_Rec_427786,Human_Splice_Rec_427808 RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_218064,RMVar_hsa_circ_80230,RMVar_hsa_circ_80291,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_218065,RMVar_hsa_circ_121534,RMVar_hsa_circ_78406,RMVar_hsa_circ_218068,RMVar_hsa_circ_352926,RMVar_hsa_circ_218070,RMVar_hsa_circ_118368,RMVar_hsa_circ_218071,RMVar_hsa_circ_218069 87251 RMVar_ID_87251 Human_SNP_ID_132428330 m1A Human chr3 + 49103961 49103961 49103961 GTCGATGGGGTCCAAGGGGTGACTCCGCACATACTCAAGGGCAGCTGAGAAGAAAGAGCCCGTGA GTCGATGGGGTCCAAGGGGTGACTCCGCACATGCTCAAGGGCAGCTGAGAAGAAAGAGCCCGTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49103830..49103995 26863196 MeRIP-seq:(Medium) rs1205366710 Functional Loss SNV dbSNP153 33..33 33 - - - 87252 RMVar_ID_87252 Human_SNP_ID_132428331 m1A Human chr3 + 49103961 49103961 49103961 GTCGATGGGGTCCAAGGGGTGACTCCGCACATACTCAAGGGCAGCTGAGAAGAAAGAGCCCGTGA GTCGATGGGGTCCAAGGGGTGACTCCGCACATTCTCAAGGGCAGCTGAGAAGAAAGAGCCCGTGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49103830..49103995 26863196 MeRIP-seq:(Medium) rs1205366710 Functional Loss SNV dbSNP153 33..33 33 - - - 87253 RMVar_ID_87253 Human_SNP_ID_132428644 m1A Human chr3 + 49104701 49104701 49104701 TCGCGGGCCTTCTGCTCGCTCAGGCCGAGGCTAGTGAAGAGCGACAGGGAGTCTAGAGCCGCCAT TCGCGGGCCTTCTGCTCGCTCAGGCCGAGGCTGGTGAAGAGCGACAGGGAGTCTAGAGCCGCCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr3:49104601..49104750;chr3:49104301..49104750;chr3:49104616..49104750;chr3:49104651..49104725 26863196,32194978 MeRIP-seq:(Medium) rs754372622 Functional Loss SNV dbSNP153 33..33 33 - - - 87254 RMVar_ID_87254 Human_SNP_ID_132431855 m1A Human chr3 - 49115827 49115825 49115828 GACAGGCCAGGAGGAGGCCCGGGCTGTGGAGAAGGATAAATCCAAGGCACGATCTGAGGACACAG GACAGGCCAGGAGGAGGCCCGGGCTGTGGAG___GATAAATCCAAGGCACGATCTGAGGACACAG CCTT C USP19 Ensembl:ENSG00000172046 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49115780..49115879 26863196 MeRIP-seq:(Medium) rs1184211930 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18007253,Human_RBP_ID_19012164,Human_RBP_ID_27822254 RMVar_hsa_circ_104557,RMVar_hsa_circ_218076,RMVar_hsa_circ_101628,RMVar_hsa_circ_218077 87255 RMVar_ID_87255 Human_SNP_ID_132433060 m1A Human chr3 + 49119277 49119277 49119277 TCTTTGTGGCCAAATTCTCCAGCAAGGAACGGACAGCCTAATGGAAAGAAGCCAGTGATCACTGC TCTTTGTGGCCAAATTCTCCAGCAAGGAACGGGCAGCCTAATGGAAAGAAGCCAGTGATCACTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49119022..49120502 26863196 MeRIP-seq:(Medium) rs545811664 Functional Loss SNV dbSNP153 33..33 33 - - - 87256 RMVar_ID_87256 Human_SNP_ID_132433610 m1A Human chr3 + 49121251 49121251 49121251 GCAGGGGTCACTGGCAGGTGTTGTAGATCTGCACCTGCAAGTTGATGGCTTGAAGCACGCTGCGC GCAGGGGTCACTGGCAGGTGTTGTAGATCTGCGCCTGCAAGTTGATGGCTTGAAGCACGCTGCGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49121226..49121250 26863196 MeRIP-seq:(Medium) rs1403522839 Functional Loss SNV dbSNP153 33..33 33 - - - 87257 RMVar_ID_87257 Human_SNP_ID_132433820 m1A Human chr3 + 49121789 49121789 49121789 CCTGCCCGTTTCAATTTCAGAGCCTCCAGGAGAGCATCCAACTGCCGAGCCCTTTCACCTGCAGA CCTGCCCGTTTCAATTTCAGAGCCTCCAGGAGGGCATCCAACTGCCGAGCCCTTTCACCTGCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49121740..49121875 26863196 MeRIP-seq:(Medium) rs112981471 Functional Loss SNV dbSNP153 33..33 33 - - - 87258 RMVar_ID_87258 Human_SNP_ID_132433828 m1A Human chr3 - 49121799 49121799 49121799 GGCACTGAGCTCTGCAGGTGAAAGGGCTCGGCAGTTGGATGCTCTCCTGGAGGCTCTGAAATTGA GGCACTGAGCTCTGCAGGTGAAAGGGCTCGGCTGTTGGATGCTCTCCTGGAGGCTCTGAAATTGA T A LAMB2 Ensembl:ENSG00000172037 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49121748..49121860 26863196 MeRIP-seq:(Medium) rs544798374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5120272,Human_RBP_ID_9141438 Human_Splice_Rec_428432,Human_Splice_Rec_428492,Human_Splice_Rec_428554,Human_Splice_Rec_428564 Human_miRNA_ID_2992198 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_125114,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_109545,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218097,RMVar_hsa_circ_218096,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_361676,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099 87259 RMVar_ID_87259 Human_SNP_ID_132433941 m1A Human chr3 - 49122060 49122059 49122061 TCCCCAGGAGCTGGGCTGAGGATGAGAAACAGAAGGCAGAGACAGTACAGGCAGCACTGGAGGAG TCCCCAGGAGCTGGGCTGAGGATGAGAAACA__AGGCAGAGACAGTACAGGCAGCACTGGAGGAG TTC T LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49121926..49122110 26863196 MeRIP-seq:(Medium) rs1560066873 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5120731,Human_RBP_ID_9354322,Human_RBP_ID_17661106,Human_RBP_ID_19012172 Human_Splice_Rec_428490,Human_Splice_Rec_428552,Human_Splice_Rec_428562 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_125114,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_109545,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218097,RMVar_hsa_circ_218096,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_81098,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099,RMVar_hsa_circ_218100,RMVar_hsa_circ_218101 87260 RMVar_ID_87260 Human_SNP_ID_132433950 m1A Human chr3 - 49122084 49122082 49122085 CCTCCAGGTTCTGATTCCCCCTTCTCCCCAGGAGCTGGGCTGAGGATGAGAAACAGAAGGCAGAG CCTCCAGGTTCTGATTCCCCCTTCTCCCCAG___CTGGGCTGAGGATGAGAAACAGAAGGCAGAG GCTC G LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49121926..49122100 32194978 MeRIP-seq:(Medium) rs1299413522 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_783941,Human_RBP_ID_835950,Human_RBP_ID_19012172,Human_RBP_ID_22824169 Human_Splice_Rec_428490,Human_Splice_Rec_428552,Human_Splice_Rec_428562 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_125114,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_109545,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218097,RMVar_hsa_circ_218096,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_81098,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099,RMVar_hsa_circ_218100,RMVar_hsa_circ_218101 87261 RMVar_ID_87261 Human_SNP_ID_132434042 m1A Human chr3 + 49122273 49122273 49122273 TCTGCCAGGCTCCGGACTCGCTCTGCAATCGCACCCGCCAGGTGCTGGATCTGCTCAGCTGAAGC TCTGCCAGGCTCCGGACTCGCTCTGCAATCGCGCCCGCCAGGTGCTGGATCTGCTCAGCTGAAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr3:49122251..49122275;chr3:49122151..49122375;chr3:49122151..49122275;chr3:49122226..49122275 26863196,32194978 MeRIP-seq:(Medium) rs3209614 Functional Loss SNV dbSNP153 33..33 33 - - - 87262 RMVar_ID_87262 Human_SNP_ID_132434221 m1A Human chr3 + 49122847 49122847 49122847 GTGCCTCGCTTGCCTGCCGACGAGTCTCAGCCACTCTGCTGAGGATGCTACCACCTTCTGCCAGT GTGCCTCGCTTGCCTGCCGACGAGTCTCAGCCGCTCTGCTGAGGATGCTACCACCTTCTGCCAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49122796..49123109 26863196 MeRIP-seq:(Medium) rs1177406934 Functional Loss SNV dbSNP153 33..33 33 - - - 87263 RMVar_ID_87263 Human_SNP_ID_132434226 m1A Human chr3 - 49122854 49122854 49122854 AGCGGGCACTGGCAGAAGGTGGTAGCATCCTCAGCAGAGTGGCTGAGACTCGTCGGCAGGCAAGC AGCGGGCACTGGCAGAAGGTGGTAGCATCCTCTGCAGAGTGGCTGAGACTCGTCGGCAGGCAAGC T A LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49122804..49123001 26863196 MeRIP-seq:(Medium) rs1466623761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5120733,Human_RBP_ID_22455829,Human_RBP_ID_22676423 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_109545,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218096,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099 87264 RMVar_ID_87264 Human_SNP_ID_132434270 m1A Human chr3 - 49122933 49122933 49122933 GGGGGCCTCAGCTGCAATGGGGCAGCGGCTACAGCAGACCTAGCACTGGGCCGGGCCCGGCACAC GGGGGCCTCAGCTGCAATGGGGCAGCGGCTACGGCAGACCTAGCACTGGGCCGGGCCCGGCACAC T C LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49122704..49123101 26863196 MeRIP-seq:(Medium) rs1459289896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18471646,Human_RBP_ID_22455830 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_109545,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218096,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099 87265 RMVar_ID_87265 Human_SNP_ID_132434394 m1A Human chr3 - 49123229 49123227 49123230 GCATCGGACAGAGGCACTGATGGATGCTCAGAAGGAGGACTTCAACAGCAAACACATGGCCAACC GCATCGGACAGAGGCACTGATGGATGCTCAG___GAGGACTTCAACAGCAAACACATGGCCAACC CCTT C LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49123178..49123328 26863196 MeRIP-seq:(Medium) rs761768465 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_428485,Human_Splice_Rec_428547 Human_miRNA_ID_2976365 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099,RMVar_hsa_circ_218102,RMVar_hsa_circ_300227 87266 RMVar_ID_87266 Human_SNP_ID_132434439 m1A Human chr3 - 49123352 49123352 49123352 GCCCAATTTAGGTGCCTATGACAGCATCCGGCATGCCCATAGCCAGTCTGCAGAGGCAGAACGTC GCCCAATTTAGGTGCCTATGACAGCATCCGGCGTGCCCATAGCCAGTCTGCAGAGGCAGAACGTC T C LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:49123301..49123375 26863196 MeRIP-seq:(Medium) rs775944984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783947 Human_Splice_Rec_428484,Human_Splice_Rec_428546,Human_Splice_Rec_428572 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_112170,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_112293,RMVar_hsa_circ_111979,RMVar_hsa_circ_106531,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_88788,RMVar_hsa_circ_89494,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218091,RMVar_hsa_circ_218093,RMVar_hsa_circ_218095,RMVar_hsa_circ_218094,RMVar_hsa_circ_218092,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_19531,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099,RMVar_hsa_circ_218102,RMVar_hsa_circ_300227 87267 RMVar_ID_87267 Human_SNP_ID_132434642 m1A Human chr3 + 49123854 49123854 49123854 GCATGTGCCAGAAGCTGCTCTCAAAGGCACCCAGCACACCCGTCTGTTGCAACTCCTGCGCCCGC GCATGTGCCAGAAGCTGCTCTCAAAGGCACCCGGCACACCCGTCTGTTGCAACTCCTGCGCCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49123803..49123951 26863196 MeRIP-seq:(Medium) rs376037354 Functional Loss SNV dbSNP153 33..33 33 - - - 87268 RMVar_ID_87268 Human_SNP_ID_132435178 m1A Human chr3 + 49125327 49125327 49125327 CAAGCGCCTGTGTGGGTGTTGCACTCATCTGCATGCCCATTGCAGACACATGGCCGGCAGCTAGG CAAGCGCCTGTGTGGGTGTTGCACTCATCTGCTTGCCCATTGCAGACACATGGCCGGCAGCTAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49125276..49125350 32194978 MeRIP-seq:(Medium) rs1167544768 Functional Loss SNV dbSNP153 33..33 33 - - - 87269 RMVar_ID_87269 Human_SNP_ID_132435223 m1A Human chr3 - 49125452 49125452 49125452 CCTGCCAGTGCAGCCACGAGGGGGCACTCAGCAGTCTCTGTGAAAAGACCAGTGGGCAATGTCTC CCTGCCAGTGCAGCCACGAGGGGGCACTCAGCCGTCTCTGTGAAAAGACCAGTGGGCAATGTCTC T G LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49125401..49125475 32194978 MeRIP-seq:(Medium) rs950013669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18339284,Human_RBP_ID_20912797 Human_Splice_Rec_428470,Human_Splice_Rec_428532,Human_Splice_Rec_428606 Human_miRNA_ID_3085447 RMVar_hsa_circ_79926,RMVar_hsa_circ_105180,RMVar_hsa_circ_119644,RMVar_hsa_circ_122631,RMVar_hsa_circ_123103,RMVar_hsa_circ_121740,RMVar_hsa_circ_111979,RMVar_hsa_circ_89587,RMVar_hsa_circ_101301,RMVar_hsa_circ_97577,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218087,RMVar_hsa_circ_218089,RMVar_hsa_circ_218090,RMVar_hsa_circ_218088,RMVar_hsa_circ_218085,RMVar_hsa_circ_218086,RMVar_hsa_circ_218084,RMVar_hsa_circ_107963,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_32995,RMVar_hsa_circ_218099,RMVar_hsa_circ_113769,RMVar_hsa_circ_90590,RMVar_hsa_circ_92444,RMVar_hsa_circ_218103,RMVar_hsa_circ_218104,RMVar_hsa_circ_113035,RMVar_hsa_circ_218106,RMVar_hsa_circ_124446,RMVar_hsa_circ_218107,RMVar_hsa_circ_218109,RMVar_hsa_circ_88781,RMVar_hsa_circ_218108 87270 RMVar_ID_87270 Human_SNP_ID_132436449 m1A Human chr3 - 49129302 49129302 49129302 TTTCGTGCAGCCTGGCCACTGGGGCCTGAGCCACGACCTGCTCGGCTGCCGCCCCTGTGACTGCG TTTCGTGCAGCCTGGCCACTGGGGCCTGAGCCTCGACCTGCTCGGCTGCCGCCCCTGTGACTGCG T A LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49129251..49129325 32194978 MeRIP-seq:(Medium) rs1131788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937971,Human_RBP_ID_22455849,Human_RBP_ID_22769197 Human_Splice_Rec_428456,Human_Splice_Rec_428457,Human_Splice_Rec_428518,Human_Splice_Rec_428519,Human_Splice_Rec_428615 Human_miRNA_ID_2268621 RMVar_hsa_circ_122631,RMVar_hsa_circ_111979,RMVar_hsa_circ_89587,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_32995,RMVar_hsa_circ_113769,RMVar_hsa_circ_90590,RMVar_hsa_circ_218103,RMVar_hsa_circ_218104,RMVar_hsa_circ_113035,RMVar_hsa_circ_218106,RMVar_hsa_circ_107863,RMVar_hsa_circ_124446,RMVar_hsa_circ_218109,RMVar_hsa_circ_88781,RMVar_hsa_circ_218108,RMVar_hsa_circ_218111,RMVar_hsa_circ_104210,RMVar_hsa_circ_218110,RMVar_hsa_circ_77913,RMVar_hsa_circ_218112,RMVar_hsa_circ_113680,RMVar_hsa_circ_102379,RMVar_hsa_circ_218113,RMVar_hsa_circ_218114 87271 RMVar_ID_87271 Human_SNP_ID_132436450 m1A Human chr3 - 49129302 49129302 49129302 TTTCGTGCAGCCTGGCCACTGGGGCCTGAGCCACGACCTGCTCGGCTGCCGCCCCTGTGACTGCG TTTCGTGCAGCCTGGCCACTGGGGCCTGAGCCGCGACCTGCTCGGCTGCCGCCCCTGTGACTGCG T C LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49129251..49129325 32194978 MeRIP-seq:(Medium) rs1131788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937971,Human_RBP_ID_22455849,Human_RBP_ID_22769197 Human_Splice_Rec_428456,Human_Splice_Rec_428457,Human_Splice_Rec_428518,Human_Splice_Rec_428519,Human_Splice_Rec_428615 Human_miRNA_ID_2268621 RMVar_hsa_circ_122631,RMVar_hsa_circ_111979,RMVar_hsa_circ_89587,RMVar_hsa_circ_85105,RMVar_hsa_circ_218083,RMVar_hsa_circ_218081,RMVar_hsa_circ_218082,RMVar_hsa_circ_218080,RMVar_hsa_circ_32995,RMVar_hsa_circ_113769,RMVar_hsa_circ_90590,RMVar_hsa_circ_218103,RMVar_hsa_circ_218104,RMVar_hsa_circ_113035,RMVar_hsa_circ_218106,RMVar_hsa_circ_107863,RMVar_hsa_circ_124446,RMVar_hsa_circ_218109,RMVar_hsa_circ_88781,RMVar_hsa_circ_218108,RMVar_hsa_circ_218111,RMVar_hsa_circ_104210,RMVar_hsa_circ_218110,RMVar_hsa_circ_77913,RMVar_hsa_circ_218112,RMVar_hsa_circ_113680,RMVar_hsa_circ_102379,RMVar_hsa_circ_218113,RMVar_hsa_circ_218114 87272 RMVar_ID_87272 Human_SNP_ID_132437154 m1A Human chr3 + 49131438 49131438 49131438 GGATAGGGATGGCAGGGTCCAGCACACGATAGATGACCTGGAGAAGCAGGGAGTTCATAGTCACA GGATAGGGATGGCAGGGTCCAGCACACGATAGGTGACCTGGAGAAGCAGGGAGTTCATAGTCACA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49131426..49131450 26863196 MeRIP-seq:(Medium) rs1037588990 Functional Loss SNV dbSNP153 33..33 33 - - - 87273 RMVar_ID_87273 Human_SNP_ID_132437245 m1A Human chr3 + 49131664 49131664 49131664 GCCCCACAGTCATAGGAGAAATATCGGTACACATGCCAGGTGCGGCCAAAGTCTGCTGAGCGTTC GCCCCACAGTCATAGGAGAAATATCGGTACACGTGCCAGGTGCGGCCAAAGTCTGCTGAGCGTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49131526..49131675 32194978 MeRIP-seq:(Medium) rs1331458305 Functional Loss SNV dbSNP153 33..33 33 - - - 87274 RMVar_ID_87274 Human_SNP_ID_132437380 m1A Human chr3 + 49132188 49132187 49132188 TCCAGGTCCAGCTGGATGGTGACCGCAGGGATACCTGGGACAGGAATCGGAAGTCAAGGACTCAA TCCAGGTCCAGCTGGATGGTGACCGCAGGGAT_CCTGGGACAGGAATCGGAAGTCAAGGACTCAA TA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49132101..49132200 32194978 MeRIP-seq:(Medium) rs1299227355 Functional Loss DEL dbSNP153 33..33 33 - - - 87275 RMVar_ID_87275 Human_SNP_ID_132437542 m1A Human chr3 + 49132551 49132551 49132551 TGGGGGCCATTCAGGCCACAAGTGGATGAGGCAGTCAGTCTGTCAGCTCGGCCCACCAGCAGGTC TGGGGGCCATTCAGGCCACAAGTGGATGAGGCGGTCAGTCTGTCAGCTCGGCCCACCAGCAGGTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49132526..49132550 26863196 MeRIP-seq:(Medium) rs200171185 Functional Loss SNV dbSNP153 33..33 33 - - - 87276 RMVar_ID_87276 Human_SNP_ID_132437573 m1A Human chr3 + 49132624 49132624 49132624 CGGGGTAGCAGCTTCCCCTGGAACAGCCAGGCACATCCGGGGCAGGGGCCTGTGCCAGTGTGGCA CGGGGTAGCAGCTTCCCCTGGAACAGCCAGGCGCATCCGGGGCAGGGGCCTGTGCCAGTGTGGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49132501..49132677 26863196 MeRIP-seq:(Medium) rs577456934 Functional Loss SNV dbSNP153 33..33 33 - - - 87277 RMVar_ID_87277 Human_SNP_ID_132437574 m1A Human chr3 + 49132624 49132624 49132624 CGGGGTAGCAGCTTCCCCTGGAACAGCCAGGCACATCCGGGGCAGGGGCCTGTGCCAGTGTGGCA CGGGGTAGCAGCTTCCCCTGGAACAGCCAGGCTCATCCGGGGCAGGGGCCTGTGCCAGTGTGGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49132501..49132677 26863196 MeRIP-seq:(Medium) rs577456934 Functional Loss SNV dbSNP153 33..33 33 - - - 87278 RMVar_ID_87278 Human_SNP_ID_132437583 m1A Human chr3 + 49132635 49132635 49132635 CTTCCCCTGGAACAGCCAGGCACATCCGGGGCAGGGGCCTGTGCCAGTGTGGCAGCCAGCACTGG CTTCCCCTGGAACAGCCAGGCACATCCGGGGCGGGGGCCTGTGCCAGTGTGGCAGCCAGCACTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49132586..49132677 26863196 MeRIP-seq:(Medium) rs1179045927 Functional Loss SNV dbSNP153 33..33 33 - - - 87279 RMVar_ID_87279 Human_SNP_ID_132437686 m1A Human chr3 - 49132979 49132979 49132979 TGGACAGACCTGGGAACTGACAGAGGGCCTGGAGGGAAACAGGCCAAAGACCCACAGGCAGAGTT TGGACAGACCTGGGAACTGACAGAGGGCCTGGTGGGAAACAGGCCAAAGACCCACAGGCAGAGTT T A LAMB2 Ensembl:ENSG00000172037 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:49132801..49133050;chr3:49132826..49133050 26863196 MeRIP-seq:(Medium) rs546461860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783962,Human_RBP_ID_835971,Human_RBP_ID_9393629 Clinvar_Rec_474 RMVar_hsa_circ_85105,RMVar_hsa_circ_218080 87280 RMVar_ID_87280 Human_SNP_ID_132445581 m1A Human chr3 - 49163797 49163797 49163797 AAGCATCCACACCAGCCCTTGCCAAGCATGCTACCACCAACCTGCTGCTGAGCTCTCTGAAGCAA AAGCATCCACACCAGCCCTTGCCAAGCATGCTGCCACCAACCTGCTGCTGAGCTCTCTGAAGCAA T C CCDC71 Ensembl:ENSG00000177352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49163746..49163890 26863196 MeRIP-seq:(Medium) rs374351971 Functional Loss SNV dbSNP153 33..33 33 - - - 87281 RMVar_ID_87281 Human_SNP_ID_132445582 m1A Human chr3 - 49163797 49163797 49163797 AAGCATCCACACCAGCCCTTGCCAAGCATGCTACCACCAACCTGCTGCTGAGCTCTCTGAAGCAA AAGCATCCACACCAGCCCTTGCCAAGCATGCTCCCACCAACCTGCTGCTGAGCTCTCTGAAGCAA T G CCDC71 Ensembl:ENSG00000177352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49163746..49163890 26863196 MeRIP-seq:(Medium) rs374351971 Functional Loss SNV dbSNP153 33..33 33 - - - 87282 RMVar_ID_87282 Human_SNP_ID_132445704 m1A Human chr3 + 49164203 49164203 49164203 ACAGCTTTTTCCTCCACATGCTGAACCACCACACTCATGGCATTAGGCACTGCAGATCTGCCTGG ACAGCTTTTTCCTCCACATGCTGAACCACCACCCTCATGGCATTAGGCACTGCAGATCTGCCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49164153..49164241 26863196 MeRIP-seq:(Medium) rs1477458303 Functional Loss SNV dbSNP153 33..33 33 - - - 87283 RMVar_ID_87283 Human_SNP_ID_132446293 m1A Human chr3 + 49166287 49166287 49166287 GCTCCAACCTACCGGCGCCGCCGCGGGGACCCAAGACGCGCCTCTGCGCCGCCTCCGCTGCTCCA GCTCCAACCTACCGGCGCCGCCGCGGGGACCCCAGACGCGCCTCTGCGCCGCCTCCGCTGCTCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:49166190..49166296;chr3:49166200..49166290 26863196 MeRIP-seq:(Medium) rs1025809512 Functional Loss SNV dbSNP153 33..33 33 - - - 87284 RMVar_ID_87284 Human_SNP_ID_132447523 m1A Human chr3 + 49171670 49171670 49171670 AGGCGGAACGGCGGACCCCGTACCCTGGCAGCATCGGAGCACCGGCGGGTGAGTCCCGCGGGAAC AGGCGGAACGGCGGACCCCGTACCCTGGCAGCGTCGGAGCACCGGCGGGTGAGTCCCGCGGGAAC A G KLHDC8B Ensembl:ENSG00000185909 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49171619..49171699 26863196 MeRIP-seq:(Medium) rs1256429816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784850,Human_RBP_ID_4757225 Human_Splice_Rec_428633,Human_Splice_Rec_428643 87285 RMVar_ID_87285 Human_SNP_ID_132447526 m1A Human chr3 + 49171678 49171676 49171678 CGGCGGACCCCGTACCCTGGCAGCATCGGAGCACCGGCGGGTGAGTCCCGCGGGAACCGCGCTCA CGGCGGACCCCGTACCCTGGCAGCATCGGAG__CCGGCGGGTGAGTCCCGCGGGAACCGCGCTCA GCA G KLHDC8B Ensembl:ENSG00000185909 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49171628..49171707 26863196 MeRIP-seq:(Medium) rs908229010 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_784850,Human_RBP_ID_4757225 Human_Splice_Rec_428633,Human_Splice_Rec_428643 87286 RMVar_ID_87286 Human_SNP_ID_132474663 m1A Human chr3 - 49277103 49277085 49277103 GGCCAGCGGCCTGGGAGCCGCGGTGGGGCGGGAGGCAGCGGCGGGGCGGGCCAGGAAGCTGTGGG GGCCAGCGGCCTGGGAGCCGCGGTGGGGCGGG__________________CCAGGAAGCTGTGGG GCCCGCCCCGCCGCTGCCT G C3orf62 Ensembl:ENSG00000188315 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49277058..49277204 26863196 MeRIP-seq:(Medium) rs919800739 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_266520,Human_RBP_ID_8209294,Human_RBP_ID_22726131,Human_RBP_ID_26790679 87287 RMVar_ID_87287 Human_SNP_ID_132474737 m1A Human chr3 + 49277190 49277186 49277191 GAGTCGGCAGCCACGTCCTTGTCCTCACCCGCAGCGCAGTGACGCCGACCCATCCAACGGTCATC GAGTCGGCAGCCACGTCCTTGTCCTCACC_____CGCAGTGACGCCGACCCATCCAACGGTCATC CCGCAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49277081..49277262 26863196 MeRIP-seq:(Medium) rs771642653 Functional Loss DEL dbSNP153 30..34 33 - - - 87288 RMVar_ID_87288 Human_SNP_ID_132489665 m1A Human chr3 - 49335594 49335594 49335594 CTGCTACAGTAAATTTCTGTCTCTCTCTAGGTATCTTATTGACAGCCGGTGGTTCAAGCAGTGGA CTGCTACAGTAAATTTCTGTCTCTCTCTAGGTGTCTTATTGACAGCCGGTGGTTCAAGCAGTGGA T C USP4 Ensembl:ENSG00000114316 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49335551..49340170 26863196 MeRIP-seq:(Medium) rs202118743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393631,Human_RBP_ID_18423978,Human_RBP_ID_24382987,Human_RBP_ID_26346912 Human_Splice_Rec_428744,Human_Splice_Rec_428786,Human_Splice_Rec_428918,Human_Splice_Rec_428930,Human_Splice_Rec_428952 RMVar_hsa_circ_98939,RMVar_hsa_circ_218124,RMVar_hsa_circ_99739,RMVar_hsa_circ_218141,RMVar_hsa_circ_38739,RMVar_hsa_circ_310236,RMVar_hsa_circ_115969,RMVar_hsa_circ_359146,RMVar_hsa_circ_218159 87289 RMVar_ID_87289 Human_SNP_ID_132490842 m1A Human chr3 - 49340016 49340016 49340016 GGCTGGGCCGGGGCCGCGGAGGAGATGGCGGAAGGTGGAGGCTGCCGTGAGCGACCGGATGCGGA GGCTGGGCCGGGGCCGCGGAGGAGATGGCGGATGGTGGAGGCTGCCGTGAGCGACCGGATGCGGA T A USP4 Ensembl:ENSG00000114316 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49339926..49340159 26863196 MeRIP-seq:(Medium) rs764142259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247163,Human_RBP_ID_783055,Human_RBP_ID_836053,Human_RBP_ID_4757227,Human_RBP_ID_9393632,Human_RBP_ID_18424481,Human_RBP_ID_23026622,Human_RBP_ID_26348132 Human_Splice_Rec_428743,Human_Splice_Rec_428785,Human_Splice_Rec_428891,Human_Splice_Rec_428917,Human_Splice_Rec_428929,Human_Splice_Rec_428943 RMVar_hsa_circ_99739,RMVar_hsa_circ_218141 87290 RMVar_ID_87290 Human_SNP_ID_132490843 m1A Human chr3 - 49340016 49340016 49340016 GGCTGGGCCGGGGCCGCGGAGGAGATGGCGGAAGGTGGAGGCTGCCGTGAGCGACCGGATGCGGA GGCTGGGCCGGGGCCGCGGAGGAGATGGCGGAGGGTGGAGGCTGCCGTGAGCGACCGGATGCGGA T C USP4 Ensembl:ENSG00000114316 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49339926..49340159 26863196 MeRIP-seq:(Medium) rs764142259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247163,Human_RBP_ID_783055,Human_RBP_ID_836053,Human_RBP_ID_4757227,Human_RBP_ID_9393632,Human_RBP_ID_18424481,Human_RBP_ID_23026622,Human_RBP_ID_26348132 Human_Splice_Rec_428743,Human_Splice_Rec_428785,Human_Splice_Rec_428891,Human_Splice_Rec_428917,Human_Splice_Rec_428929,Human_Splice_Rec_428943 RMVar_hsa_circ_99739,RMVar_hsa_circ_218141 87291 RMVar_ID_87291 Human_SNP_ID_132495420 m1A Human chr3 - 49357287 49357287 49357287 GGGTGTTTCCTCTAAACCTACGAGGGAGGAACACCTGATCTTACAGAAAATACCACCTCGAGATG GGGTGTTTCCTCTAAACCTACGAGGGAGGAACCCCTGATCTTACAGAAAATACCACCTCGAGATG T G GPX1 Ensembl:ENSG00000233276 Pseudogene 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49357237..49357348 26863196 MeRIP-seq:(Medium) rs1050569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604156,Human_RBP_ID_1205788,Human_RBP_ID_1386209,Human_RBP_ID_1628516,Human_RBP_ID_1964612,Human_RBP_ID_2789134,Human_RBP_ID_8574868,Human_RBP_ID_17704257,Human_RBP_ID_18007314,Human_RBP_ID_18810457,Human_RBP_ID_22090174,Human_RBP_ID_22282835,Human_RBP_ID_25742212,Human_RBP_ID_26512114,Human_RBP_ID_27055357,Human_RBP_ID_27319831,Human_RBP_ID_27502881 RMVar_hsa_circ_83995,RMVar_hsa_circ_120331,RMVar_hsa_circ_218160,RMVar_hsa_circ_218161 87292 RMVar_ID_87292 Human_SNP_ID_132495449 m1A Human chr3 + 49357351 49357351 49357351 CTCATAGATGAAAACCCCCCCGAGACAGCAGCACTGCAACTGCCAAGCAGCCGGGGTAGGAGGGG CTCATAGATGAAAACCCCCCCGAGACAGCAGCCCTGCAACTGCCAAGCAGCCGGGGTAGGAGGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49357301..49357350 26863196 MeRIP-seq:(Medium) rs531711260 Functional Loss SNV dbSNP153 33..33 33 - - - 87293 RMVar_ID_87293 Human_SNP_ID_132495536 m1A Human chr3 - 49357506 49357506 49357506 GGTGTGTCGCAACGATGTTGCCTGGAACTTTGAGAAGTTCCTGGTGGGCCCTGACGGTGTGCCCC GGTGTGTCGCAACGATGTTGCCTGGAACTTTGTGAAGTTCCTGGTGGGCCCTGACGGTGTGCCCC T A GPX1 Ensembl:ENSG00000233276 Pseudogene CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs771810430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604164,Human_RBP_ID_8574872,Human_RBP_ID_22092747 Human_miRNA_ID_2352878,Human_miRNA_ID_2352879,Human_miRNA_ID_3087480,Human_miRNA_ID_3087481 RMVar_hsa_circ_83995,RMVar_hsa_circ_120331,RMVar_hsa_circ_218160,RMVar_hsa_circ_218161 87294 RMVar_ID_87294 Human_SNP_ID_132495901 m1A Human chr3 + 49358145 49358143 49358145 AGTCCCGGACCGTGGTGCCTCAGAGGGACGCCACATTCTCGATAAGTAGTACCTTGCCCCGCAGG AGTCCCGGACCGTGGTGCCTCAGAGGGACGC__CATTCTCGATAAGTAGTACCTTGCCCCGCAGG CCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr3:49358076..49358150;chr3:49358076..49358350 26863196 MeRIP-seq:(Medium) rs1236412278 Functional Loss DEL dbSNP153 32..33 33 - - - 87295 RMVar_ID_87295 Human_SNP_ID_132495909 m1A Human chr3 + 49358154 49358154 49358154 CCGTGGTGCCTCAGAGGGACGCCACATTCTCGATAAGTAGTACCTTGCCCCGCAGGGAGCCCAGG CCGTGGTGCCTCAGAGGGACGCCACATTCTCGGTAAGTAGTACCTTGCCCCGCAGGGAGCCCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49358089..49358350 26863196 MeRIP-seq:(Medium) rs778272154 Functional Loss SNV dbSNP153 33..33 33 - - - 87296 RMVar_ID_87296 Human_SNP_ID_132495968 m1A Human chr3 + 49358228 49358228 49358228 TCCCCGCCGGCCAGCGGGCGCGCCGAGAAGGCATACACCGACTGGGCCGCCGCCGCCGCCGCCGC TCCCCGCCGGCCAGCGGGCGCGCCGAGAAGGCGTACACCGACTGGGCCGCCGCCGCCGCCGCCGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49358201..49358250 26863196 MeRIP-seq:(Medium) rs1247384703 Functional Loss SNV dbSNP153 33..33 33 - - - 87297 RMVar_ID_87297 Human_SNP_ID_132495969 m1A Human chr3 + 49358228 49358228 49358228 TCCCCGCCGGCCAGCGGGCGCGCCGAGAAGGCATACACCGACTGGGCCGCCGCCGCCGCCGCCGC TCCCCGCCGGCCAGCGGGCGCGCCGAGAAGGCTTACACCGACTGGGCCGCCGCCGCCGCCGCCGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49358201..49358250 26863196 MeRIP-seq:(Medium) rs1247384703 Functional Loss SNV dbSNP153 33..33 33 - - - 87298 RMVar_ID_87298 Human_SNP_ID_132496481 m1A Human chr3 - 49359450 49359450 49359450 CGTTTTGTCACTTTTTCTGATAAAAGATGGCCATATTACCCCTTTTCGGCCCCATGTATCTCAGT CGTTTTGTCACTTTTTCTGATAAAAGATGGCCGTATTACCCCTTTTCGGCCCCATGTATCTCAGT T C RHOA Ensembl:ENSG00000067560 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49359401..49359500 32194978 MeRIP-seq:(Medium) rs1331050076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604184,Human_RBP_ID_1205791,Human_RBP_ID_3710299,Human_RBP_ID_4746419,Human_RBP_ID_7204735,Human_RBP_ID_8209722,Human_RBP_ID_14866351,Human_RBP_ID_17025307,Human_RBP_ID_17290476,Human_RBP_ID_17403787,Human_RBP_ID_17520297,Human_RBP_ID_18007322,Human_RBP_ID_18339323,Human_RBP_ID_20913019,Human_RBP_ID_22509675,Human_RBP_ID_22824181,Human_RBP_ID_23189611,Human_RBP_ID_24007910,Human_RBP_ID_24427988,Human_RBP_ID_24498332,Human_RBP_ID_26508418,Human_RBP_ID_26685317,Human_RBP_ID_27502898,Human_RBP_ID_27719292 Human_miRNA_ID_878845,Human_miRNA_ID_1811665,Human_miRNA_ID_2392489 RMVar_hsa_circ_86940,RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_103458,RMVar_hsa_circ_90043,RMVar_hsa_circ_218163,RMVar_hsa_circ_84516,RMVar_hsa_circ_86146,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218164,RMVar_hsa_circ_218162 87299 RMVar_ID_87299 Human_SNP_ID_132496556 m1A Human chr3 + 49359727 49359727 49359727 CACAGAACTGTAACTCTGCCACAGCTGCATGAACTTGGGCTTTTCTGGTTGAGCCCATTTTCAAA CACAGAACTGTAACTCTGCCACAGCTGCATGATCTTGGGCTTTTCTGGTTGAGCCCATTTTCAAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49359601..49359775 32194978 MeRIP-seq:(Medium) rs560386296 Functional Loss SNV dbSNP153 33..33 33 - - - 87300 RMVar_ID_87300 Human_SNP_ID_132499019 m1A Human chr3 + 49368542 49368542 49368542 ATCTTCCTGCCCAGCTGTGTCCCACAAAGCCAACTCTACCTGTAATGGGAAAAACAACCACAAGA ATCTTCCTGCCCAGCTGTGTCCCACAAAGCCAGCTCTACCTGTAATGGGAAAAACAACCACAAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr3:49368376..49368602;chr3:49368426..49368550 26863196,32194978 MeRIP-seq:(Medium) rs762006336 Functional Loss SNV dbSNP153 33..33 33 - - - 87301 RMVar_ID_87301 Human_SNP_ID_132512389 m1A Human chr3 + 49411887 49411887 49411887 CGGGGACGCCGGTCCGCGAGTCGCAAACTCGGAGACGAAGGCGGGTAGCTGAAGACCAGACCGTG CGGGGACGCCGGTCCGCGAGTCGCAAACTCGGCGACGAAGGCGGGTAGCTGAAGACCAGACCGTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49411801..49412000 26863196 MeRIP-seq:(Medium) rs979128821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5425814,Human_RBP_ID_5447667,Human_RBP_ID_5474376,Human_RBP_ID_5506521 87302 RMVar_ID_87302 Human_SNP_ID_132512399 m1A Human chr3 + 49411914 49411914 49411914 CTCGGAGACGAAGGCGGGTAGCTGAAGACCAGACCGTGGACTAACGAGAGAACCGACGGAGGACC CTCGGAGACGAAGGCGGGTAGCTGAAGACCAGGCCGTGGACTAACGAGAGAACCGACGGAGGACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49411865..49412025 26863196 MeRIP-seq:(Medium) rs1413889289 Functional Loss SNV dbSNP153 33..33 33 - - - 87303 RMVar_ID_87303 Human_SNP_ID_132512436 m1A Human chr3 + 49411970 49411968 49411970 CGGAGGACCGCGGGCGGCGGGAGGGTAGCGCGAGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG CGGAGGACCGCGGGCGGCGGGAGGGTAGCGC__GAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG CGA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:49411926..49412000 26863196 MeRIP-seq:(Medium) rs1407867472 Functional Loss DEL dbSNP153 32..33 33 - - - 87304 RMVar_ID_87304 Human_SNP_ID_132512439 m1A Human chr3 + 49411970 49411970 49411970 CGGAGGACCGCGGGCGGCGGGAGGGTAGCGCGAGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG CGGAGGACCGCGGGCGGCGGGAGGGTAGCGCGCGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:49411926..49412000 26863196 MeRIP-seq:(Medium) rs978554175 Functional Loss SNV dbSNP153 33..33 33 - - - 87305 RMVar_ID_87305 Human_SNP_ID_132512440 m1A Human chr3 + 49411970 49411970 49411970 CGGAGGACCGCGGGCGGCGGGAGGGTAGCGCGAGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG CGGAGGACCGCGGGCGGCGGGAGGGTAGCGCGTGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:49411926..49412000 26863196 MeRIP-seq:(Medium) rs978554175 Functional Loss SNV dbSNP153 33..33 33 - - - 87306 RMVar_ID_87306 Human_SNP_ID_132512449 m1A Human chr3 + 49411978 49411978 49411978 CGCGGGCGGCGGGAGGGTAGCGCGAGAGAGCGAGGGCGGGCGGCGGCGGGAGGGCGGGGAACGAC CGCGGGCGGCGGGAGGGTAGCGCGAGAGAGCGCGGGCGGGCGGCGGCGGGAGGGCGGGGAACGAC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:49411876..49412075 26863410 MeRIP-seq:(Medium) rs913448650 Functional Loss SNV dbSNP153 33..33 33 - - - 87307 RMVar_ID_87307 Human_SNP_ID_132512476 m1A Human chr3 + 49412006 49412006 49412006 AGCGAGGGCGGGCGGCGGCGGGAGGGCGGGGAACGACGTGCGCGCCTCCGAGTGCCCAGCGGGCT AGCGAGGGCGGGCGGCGGCGGGAGGGCGGGGACCGACGTGCGCGCCTCCGAGTGCCCAGCGGGCT A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:49411915..49412031 26863410 MeRIP-seq:(Medium) rs1005606653 Functional Loss SNV dbSNP153 33..33 33 - - - 87308 RMVar_ID_87308 Human_SNP_ID_132512697 m1A Human chr3 - 49412476 49412476 49412476 CCCGCAAGAACTCGCTGCCCAGCGCGCCCAGCACCGTGGCCGGCAGAGCCTGCAAGGCCTGCCCA CCCGCAAGAACTCGCTGCCCAGCGCGCCCAGCGCCGTGGCCGGCAGAGCCTGCAAGGCCTGCCCA T C RHOA Ensembl:ENSG00000067560 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49412430..49412563 26863196 MeRIP-seq:(Medium) rs768166136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_429003 87309 RMVar_ID_87309 Human_SNP_ID_132544553 m1A Human chr3 - 49531452 49531452 49531452 CAATGGCAGTGACAGGTGTGGGTGTAGCATGGATCTGCCTCCGGACGCGTTTGGGAAGAGGGGGC CAATGGCAGTGACAGGTGTGGGTGTAGCATGGTTCTGCCTCCGGACGCGTTTGGGAAGAGGGGGC T A BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49531402..49531603 26863196 MeRIP-seq:(Medium) rs1201828424 Functional Loss SNV dbSNP153 33..33 33 - - - 87310 RMVar_ID_87310 Human_SNP_ID_132544666 m1A Human chr3 + 49531751 49531751 49531751 CAACGATGACCATTCCTGGCTATGTGGAGCCTACTGCAGTTGCTACCCCTCCCACAACCACCACC CAACGATGACCATTCCTGGCTATGTGGAGCCTTCTGCAGTTGCTACCCCTCCCACAACCACCACC A T DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:49531701..49531775 26863196 MeRIP-seq:(Medium) rs768983113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1964675,Human_RBP_ID_7205051,Human_RBP_ID_17290504,Human_RBP_ID_17403807,Human_RBP_ID_17520326,Human_RBP_ID_18007381,Human_RBP_ID_27502974 Clinvar_Rec_475 87311 RMVar_ID_87311 Human_SNP_ID_132544685 m1A Human chr3 - 49531799 49531799 49531799 GTCAGTTGAAGGCGTTGCTGGTTTTGGTGTGGATACTCGTGGCTTCTTGGTGGTGGTTGTGGGAG GTCAGTTGAAGGCGTTGCTGGTTTTGGTGTGGGTACTCGTGGCTTCTTGGTGGTGGTTGTGGGAG T C BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:49531776..49531800 26863196 MeRIP-seq:(Medium) rs755602029 Functional Loss SNV dbSNP153 33..33 33 - - - 87312 RMVar_ID_87312 Human_SNP_ID_132544690 m1A Human chr3 + 49531817 49531817 49531817 AGAAGCCACGAGTATCCACACCAAAACCAGCAACGCCTTCAACTGACTCCACCACCACCACGACT AGAAGCCACGAGTATCCACACCAAAACCAGCAGCGCCTTCAACTGACTCCACCACCACCACGACT A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49531769..49531940 26863196 MeRIP-seq:(Medium) rs149838438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628593,Human_RBP_ID_17194907,Human_RBP_ID_17290505,Human_RBP_ID_17403808,Human_RBP_ID_18209901,Human_RBP_ID_27502979 Clinvar_Rec_476 87313 RMVar_ID_87313 Human_SNP_ID_132544694 m1A Human chr3 + 49531826 49531826 49531826 GAGTATCCACACCAAAACCAGCAACGCCTTCAACTGACTCCACCACCACCACGACTCGCAGGCCA GAGTATCCACACCAAAACCAGCAACGCCTTCAGCTGACTCCACCACCACCACGACTCGCAGGCCA A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:49531356..49532221;chr3:49531715..49531976;chr3:49531700..49531933 26863196 MeRIP-seq:(Medium) rs747370227 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_70267,Human_RBP_ID_1628593,Human_RBP_ID_17194907,Human_RBP_ID_17290505,Human_RBP_ID_17403808,Human_RBP_ID_18209901,Human_RBP_ID_27502979 87314 RMVar_ID_87314 Human_SNP_ID_132544712 m1A Human chr3 + 49531867 49531867 49531867 ACCACCACCACGACTCGCAGGCCAACCAAGAAACCACGGACACCCCGGCCAGTGCCCCGGGTCAC ACCACCACCACGACTCGCAGGCCAACCAAGAAGCCACGGACACCCCGGCCAGTGCCCCGGGTCAC A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:49531715..49531939 26863196 MeRIP-seq:(Medium) rs201720631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17292683,Human_RBP_ID_20786803,Human_RBP_ID_27502981 87315 RMVar_ID_87315 Human_SNP_ID_132545190 m1A Human chr3 - 49533051 49533051 49533051 GATCCTCATCCCGCAGGGGCGTGTACTCTCCCATGGTGTCCTGGTTCAGAGGAGTGGTCTCGGGC GATCCTCATCCCGCAGGGGCGTGTACTCTCCCTTGGTGTCCTGGTTCAGAGGAGTGGTCTCGGGC T A BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:49533026..49533050 26863196 MeRIP-seq:(Medium) rs1218884146 Functional Loss SNV dbSNP153 33..33 33 - - - 87316 RMVar_ID_87316 Human_SNP_ID_132545192 m1A Human chr3 + 49533055 49533055 49533055 GAGACCACTCCTCTGAACCAGGACACCATGGGAGAGTACACGCCCCTGCGGGATGAGGATCCCAA GAGACCACTCCTCTGAACCAGGACACCATGGGGGAGTACACGCCCCTGCGGGATGAGGATCCCAA A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:49533004..49533147 26863196 MeRIP-seq:(Medium) rs746855029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7205061,Human_RBP_ID_14868956,Human_RBP_ID_17292386,Human_RBP_ID_18954358,Human_RBP_ID_22455868,Human_RBP_ID_22769218,Human_RBP_ID_27319926,Human_RBP_ID_27503024 87317 RMVar_ID_87317 Human_SNP_ID_132545219 m1A Human chr3 + 49533099 49533099 49533099 CCTGCGGGATGAGGATCCCAATGCGCCTCCCTACCAGCCCCCACCGCCCTTCACAGCACCCATGG CCTGCGGGATGAGGATCCCAATGCGCCTCCCTGCCAGCCCCCACCGCCCTTCACAGCACCCATGG A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49533009..49533137 26863196 MeRIP-seq:(Medium) rs1436774690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248543,Human_RBP_ID_17292386,Human_RBP_ID_18007389,Human_RBP_ID_22769218,Human_RBP_ID_27319926,Human_RBP_ID_27503024 Clinvar_Rec_477 87318 RMVar_ID_87318 Human_SNP_ID_132545226 m1A Human chr3 + 49533121 49533121 49533121 GCGCCTCCCTACCAGCCCCCACCGCCCTTCACAGCACCCATGGAGGGCAAGGGCTCCCGTCCCAA GCGCCTCCCTACCAGCCCCCACCGCCCTTCACCGCACCCATGGAGGGCAAGGGCTCCCGTCCCAA A C DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49532920..49533360 26863196 MeRIP-seq:(Medium) rs779926178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17292686,Human_RBP_ID_22769219,Human_RBP_ID_24498362,Human_RBP_ID_27319926,Human_RBP_ID_27503024 87319 RMVar_ID_87319 Human_SNP_ID_132545252 m1A Human chr3 - 49533196 49533196 49533196 TACCCTGCCTCCACCCAGGCGCTTGCGGGTTAAGGTGGGACATAGGGAGGAGGTGACCGGTATGG TACCCTGCCTCCACCCAGGCGCTTGCGGGTTATGGTGGGACATAGGGAGGAGGTGACCGGTATGG T A BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:49533176..49533200 26863196 MeRIP-seq:(Medium) rs188360938 Functional Loss SNV dbSNP153 33..33 33 - - - 87320 RMVar_ID_87320 Human_SNP_ID_132545277 m1A Human chr3 - 49533251 49533251 49533251 TCTGCAGGCCACCGGTCTCCACAGACAACACCATGTCGTCTCCAGGCCCCTGCCCTACCCTGCCT TCTGCAGGCCACCGGTCTCCACAGACAACACCTTGTCGTCTCCAGGCCCCTGCCCTACCCTGCCT T A BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:49533226..49533250 26863196 MeRIP-seq:(Medium) rs935636075 Functional Loss SNV dbSNP153 33..33 33 - - - 87321 RMVar_ID_87321 Human_SNP_ID_132550307 m1A Human chr3 + 49554273 49554273 49554273 AGCGCGACGTCCCAGAGGCCGCTTCTAGTGGCAGGTGCCCCTCCTCACAGGGCCCTCGCAGCCCC AGCGCGACGTCCCAGAGGCCGCTTCTAGTGGCGGGTGCCCCTCCTCACAGGGCCCTCGCAGCCCC A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49554224..49554320 26863196 MeRIP-seq:(Medium) rs1459863839 Functional Loss SNV dbSNP153 33..33 33 - - - 87322 RMVar_ID_87322 Human_SNP_ID_132580466 m1A Human chr3 - 49675185 49675185 49675185 GTTCTCCATGCGTTCCAGGTCCCTCTGGGTCCACTCTGTGAGGGGAGGCATGAGACTGCTCACCT GTTCTCCATGCGTTCCAGGTCCCTCTGGGTCCGCTCTGTGAGGGGAGGCATGAGACTGCTCACCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49675176..49675250 26863196 MeRIP-seq:(Medium) rs1267813077 Functional Loss SNV dbSNP153 33..33 33 - - - 87323 RMVar_ID_87323 Human_SNP_ID_132580482 m1A Human chr3 + 49675235 49675235 49675235 GAACGCATGGAGAACATTCGATTCTGCCGCCAATACCTGGTGTTCCATGACGGGGACTCAGTGGT GAACGCATGGAGAACATTCGATTCTGCCGCCACTACCTGGTGTTCCATGACGGGGACTCAGTGGT A C APEH Ensembl:ENSG00000164062 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49675176..49675250 32194978 MeRIP-seq:(Medium) rs141512953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604341,Human_RBP_ID_18810565 Human_Splice_Rec_430024,Human_Splice_Rec_430032,Human_Splice_Rec_430033,Human_Splice_Rec_430118,Human_Splice_Rec_430119,Human_Splice_Rec_430172,Human_Splice_Rec_430173,Human_Splice_Rec_430202,Human_Splice_Rec_430203,Human_Splice_Rec_430208,Human_Splice_Rec_430209 RMVar_hsa_circ_49672,RMVar_hsa_circ_77835,RMVar_hsa_circ_111819,RMVar_hsa_circ_120196,RMVar_hsa_circ_95140,RMVar_hsa_circ_123247,RMVar_hsa_circ_218188,RMVar_hsa_circ_218189,RMVar_hsa_circ_218190,RMVar_hsa_circ_218187,RMVar_hsa_circ_108031,RMVar_hsa_circ_121880,RMVar_hsa_circ_91925,RMVar_hsa_circ_83852,RMVar_hsa_circ_218191,RMVar_hsa_circ_218193,RMVar_hsa_circ_218194,RMVar_hsa_circ_218192,RMVar_hsa_circ_112521,RMVar_hsa_circ_218195,RMVar_hsa_circ_218196 87324 RMVar_ID_87324 Human_SNP_ID_132580483 m1A Human chr3 + 49675235 49675235 49675235 GAACGCATGGAGAACATTCGATTCTGCCGCCAATACCTGGTGTTCCATGACGGGGACTCAGTGGT GAACGCATGGAGAACATTCGATTCTGCCGCCAGTACCTGGTGTTCCATGACGGGGACTCAGTGGT A G APEH Ensembl:ENSG00000164062 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49675176..49675250 32194978 MeRIP-seq:(Medium) rs141512953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604341,Human_RBP_ID_18810565 Human_Splice_Rec_430024,Human_Splice_Rec_430032,Human_Splice_Rec_430033,Human_Splice_Rec_430118,Human_Splice_Rec_430119,Human_Splice_Rec_430172,Human_Splice_Rec_430173,Human_Splice_Rec_430202,Human_Splice_Rec_430203,Human_Splice_Rec_430208,Human_Splice_Rec_430209 RMVar_hsa_circ_49672,RMVar_hsa_circ_77835,RMVar_hsa_circ_111819,RMVar_hsa_circ_120196,RMVar_hsa_circ_95140,RMVar_hsa_circ_123247,RMVar_hsa_circ_218188,RMVar_hsa_circ_218189,RMVar_hsa_circ_218190,RMVar_hsa_circ_218187,RMVar_hsa_circ_108031,RMVar_hsa_circ_121880,RMVar_hsa_circ_91925,RMVar_hsa_circ_83852,RMVar_hsa_circ_218191,RMVar_hsa_circ_218193,RMVar_hsa_circ_218194,RMVar_hsa_circ_218192,RMVar_hsa_circ_112521,RMVar_hsa_circ_218195,RMVar_hsa_circ_218196 87325 RMVar_ID_87325 Human_SNP_ID_132580643 m1A Human chr3 + 49675755 49675755 49675755 CCATGAAAGCTGTGCTGCGCAAGGCTGGAGGCACGGGCCCTGGGGAAGAGAAGCAGTTCCTGGAG CCATGAAAGCTGTGCTGCGCAAGGCTGGAGGCCCGGGCCCTGGGGAAGAGAAGCAGTTCCTGGAG A C APEH Ensembl:ENSG00000164062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr3:49675676..49675812;chr3:49675704..49675907 26863196,32194978 MeRIP-seq:(Medium) rs759386594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835872,Human_RBP_ID_19010345,Human_RBP_ID_27503093 Human_Splice_Rec_430010,Human_Splice_Rec_430011,Human_Splice_Rec_430025,Human_Splice_Rec_430034,Human_Splice_Rec_430035,Human_Splice_Rec_430072,Human_Splice_Rec_430073,Human_Splice_Rec_430090,Human_Splice_Rec_430091,Human_Splice_Rec_430098,Human_Splice_Rec_430099,Human_Splice_Rec_430120,Human_Splice_Rec_430121,Human_Splice_Rec_430160,Human_Splice_Rec_430161,Human_Splice_Rec_430174,Human_Splice_Rec_430175,Human_Splice_Rec_430184,Human_Splice_Rec_430185,Human_Splice_Rec_430204,Human_Splice_Rec_430205,Human_Splice_Rec_430210,Human_Splice_Rec_430211,Human_Splice_Rec_430221 RMVar_hsa_circ_11861,RMVar_hsa_circ_49672,RMVar_hsa_circ_77835,RMVar_hsa_circ_111819,RMVar_hsa_circ_120196,RMVar_hsa_circ_95140,RMVar_hsa_circ_123247,RMVar_hsa_circ_218188,RMVar_hsa_circ_218189,RMVar_hsa_circ_218190,RMVar_hsa_circ_218187,RMVar_hsa_circ_108031,RMVar_hsa_circ_121880,RMVar_hsa_circ_91925,RMVar_hsa_circ_103743,RMVar_hsa_circ_83852,RMVar_hsa_circ_218191,RMVar_hsa_circ_218193,RMVar_hsa_circ_218194,RMVar_hsa_circ_218192,RMVar_hsa_circ_112521,RMVar_hsa_circ_117751,RMVar_hsa_circ_218195,RMVar_hsa_circ_218196,RMVar_hsa_circ_120410,RMVar_hsa_circ_111423,RMVar_hsa_circ_87033,RMVar_hsa_circ_90040,RMVar_hsa_circ_81893,RMVar_hsa_circ_218198,RMVar_hsa_circ_218200,RMVar_hsa_circ_218202,RMVar_hsa_circ_218203,RMVar_hsa_circ_218201,RMVar_hsa_circ_218199,RMVar_hsa_circ_218197 87326 RMVar_ID_87326 Human_SNP_ID_132580815 m1A Human chr3 - 49676158 49676158 49676158 TGGCTATCTCATCATCGCTGGCACTGACGTCCAAGGCTTTGGTCTGAAAGAAGGACTCGGCCTTG TGGCTATCTCATCATCGCTGGCACTGACGTCCGAGGCTTTGGTCTGAAAGAAGGACTCGGCCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49676019..49676232 26863196 MeRIP-seq:(Medium) rs780876657 Functional Loss SNV dbSNP153 33..33 33 - - - 87327 RMVar_ID_87327 Human_SNP_ID_132580816 m1A Human chr3 - 49676158 49676158 49676158 TGGCTATCTCATCATCGCTGGCACTGACGTCCAAGGCTTTGGTCTGAAAGAAGGACTCGGCCTTG TGGCTATCTCATCATCGCTGGCACTGACGTCCCAGGCTTTGGTCTGAAAGAAGGACTCGGCCTTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49676019..49676232 26863196 MeRIP-seq:(Medium) rs780876657 Functional Loss SNV dbSNP153 33..33 33 - - - 87328 RMVar_ID_87328 Human_SNP_ID_132581029 m1A Human chr3 + 49676699 49676699 49676699 TCCGGTTGGGCATCCGCTTTTGCACCAATCGCAGGTGAGGGAGTGGGGCAAGGCAAGGGGCCTTG TCCGGTTGGGCATCCGCTTTTGCACCAATCGCGGGTGAGGGAGTGGGGCAAGGCAAGGGGCCTTG A G APEH Ensembl:ENSG00000164062 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49676426..49676725 32194978 MeRIP-seq:(Medium) rs1198956597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115530,Human_RBP_ID_22457346 Human_Splice_Rec_430018,Human_Splice_Rec_430019,Human_Splice_Rec_430042,Human_Splice_Rec_430043,Human_Splice_Rec_430078,Human_Splice_Rec_430079,Human_Splice_Rec_430106,Human_Splice_Rec_430107,Human_Splice_Rec_430128,Human_Splice_Rec_430129,Human_Splice_Rec_430166,Human_Splice_Rec_430167,Human_Splice_Rec_430190,Human_Splice_Rec_430191,Human_Splice_Rec_430216,Human_Splice_Rec_430217,Human_Splice_Rec_430226,Human_Splice_Rec_430227,Human_Splice_Rec_430235 RMVar_hsa_circ_49672,RMVar_hsa_circ_77835,RMVar_hsa_circ_95140,RMVar_hsa_circ_123247,RMVar_hsa_circ_218188,RMVar_hsa_circ_218187,RMVar_hsa_circ_108031,RMVar_hsa_circ_121880,RMVar_hsa_circ_91925,RMVar_hsa_circ_103743,RMVar_hsa_circ_83852,RMVar_hsa_circ_218191,RMVar_hsa_circ_218193,RMVar_hsa_circ_218194,RMVar_hsa_circ_218192,RMVar_hsa_circ_112521,RMVar_hsa_circ_218195,RMVar_hsa_circ_218196,RMVar_hsa_circ_120410,RMVar_hsa_circ_111423,RMVar_hsa_circ_87033,RMVar_hsa_circ_81893,RMVar_hsa_circ_90020,RMVar_hsa_circ_52285,RMVar_hsa_circ_218198,RMVar_hsa_circ_218200,RMVar_hsa_circ_218201,RMVar_hsa_circ_218199,RMVar_hsa_circ_122762,RMVar_hsa_circ_218197,RMVar_hsa_circ_79505,RMVar_hsa_circ_107435,RMVar_hsa_circ_218204,RMVar_hsa_circ_218205,RMVar_hsa_circ_218207,RMVar_hsa_circ_89088,RMVar_hsa_circ_374782,RMVar_hsa_circ_108228,RMVar_hsa_circ_218208,RMVar_hsa_circ_218209,RMVar_hsa_circ_110367,RMVar_hsa_circ_370191,RMVar_hsa_circ_99414,RMVar_hsa_circ_218213,RMVar_hsa_circ_81797,RMVar_hsa_circ_83835,RMVar_hsa_circ_218215,RMVar_hsa_circ_218217,RMVar_hsa_circ_80458,RMVar_hsa_circ_218216,RMVar_hsa_circ_218214,RMVar_hsa_circ_218211,RMVar_hsa_circ_218212,RMVar_hsa_circ_218210 87329 RMVar_ID_87329 Human_SNP_ID_132586007 m1A Human chr3 - 49691153 49691153 49691153 CCGGCCCCCTTGGATGCCATCCTTCATCTCTCATGGGCAGCCAGTGGTCCTGGGGGCTGAGCCAG CCGGCCCCCTTGGATGCCATCCTTCATCTCTCCTGGGCAGCCAGTGGTCCTGGGGGCTGAGCCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49691126..49691214 26863196 MeRIP-seq:(Medium) rs775340795 Functional Loss SNV dbSNP153 33..33 33 - - - 87330 RMVar_ID_87330 Human_SNP_ID_132594077 m1A Human chr3 + 49718825 49718825 49718825 AGTCGCAAGGCAAAGGGTTGTTGTGCAAGTAGAGGCCGTTCTTGAGGAAGGCCGGCAGCGCGGCC AGTCGCAAGGCAAAGGGTTGTTGTGCAAGTAGGGGCCGTTCTTGAGGAAGGCCGGCAGCGCGGCC A G RNF123 Ensembl:ENSG00000164068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49718822..49718926 26863196 MeRIP-seq:(Medium) rs751097518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115483,RMVar_hsa_circ_218254,RMVar_hsa_circ_100111,RMVar_hsa_circ_121749,RMVar_hsa_circ_218258,RMVar_hsa_circ_218259,RMVar_hsa_circ_218263,RMVar_hsa_circ_89934,RMVar_hsa_circ_37811,RMVar_hsa_circ_94106,RMVar_hsa_circ_83839,RMVar_hsa_circ_218267,RMVar_hsa_circ_218269,RMVar_hsa_circ_81902,RMVar_hsa_circ_218271 87331 RMVar_ID_87331 Human_SNP_ID_132595351 m1A Human chr3 + 49721854 49721854 49721854 AGGTAGAGCTCATCATTAACTATGACGTCCTCACCCAGCACTGTCACGTTCTCCATGCGTACCTC AGGTAGAGCTCATCATTAACTATGACGTCCTCGCCCAGCACTGTCACGTTCTCCATGCGTACCTC A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49721804..49721872 26863196 MeRIP-seq:(Medium) rs779167148 Functional Loss SNV dbSNP153 33..33 33 - - - 87332 RMVar_ID_87332 Human_SNP_ID_132595446 m1A Human chr3 - 49722035 49722035 49722035 TGTGTGTATCCGGCGGTGCACGGTGCTGCGGGATGCCCGGATCCGTTCCCATTCCTGGCTTGAGT TGTGTGTATCCGGCGGTGCACGGTGCTGCGGGGTGCCCGGATCCGTTCCCATTCCTGGCTTGAGT T C GMPPB Ensembl:ENSG00000173540 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49721986..49722777 32194978 MeRIP-seq:(Medium) rs1294974745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_430869,Human_Splice_Rec_430885 RMVar_hsa_circ_21442,RMVar_hsa_circ_106699,RMVar_hsa_circ_116065,RMVar_hsa_circ_218273,RMVar_hsa_circ_87617,RMVar_hsa_circ_218274,RMVar_hsa_circ_218272 87333 RMVar_ID_87333 Human_SNP_ID_132596201 m1A Human chr3 - 49723803 49723803 49723803 GTGAAGGGCGCGGGGCCGGGCACGGCGTTGGGAGTGCGCGGCAGGGACCGGCCAGGCGGGCTGCA GTGAAGGGCGCGGGGCCGGGCACGGCGTTGGGCGTGCGCGGCAGGGACCGGCCAGGCGGGCTGCA T G GMPPB Ensembl:ENSG00000173540 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:49723701..49723903 26863410 MeRIP-seq:(Medium) rs1443199547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156003,Human_RBP_ID_247839,Human_RBP_ID_939369,Human_RBP_ID_3965250,Human_RBP_ID_4746957,Human_RBP_ID_5325587,Human_RBP_ID_5390118,Human_RBP_ID_18424219 Human_miRNA_ID_2085264 RMVar_hsa_circ_106699,RMVar_hsa_circ_218274 87334 RMVar_ID_87334 Human_SNP_ID_132612593 m1A Human chr3 + 49786456 49786456 49786456 GCCCGCCCCCTGGCAGGCAGCACAGGTGGCTGAGCACCGCTACAGCGGCCTCTCACCGGCCGCTT GCCCGCCCCCTGGCAGGCAGCACAGGTGGCTGGGCACCGCTACAGCGGCCTCTCACCGGCCGCTT A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49786406..49786481 26863196 MeRIP-seq:(Medium) rs940190193 Functional Loss SNV dbSNP153 33..33 33 - - - 87335 RMVar_ID_87335 Human_SNP_ID_132617855 m1A Human chr3 + 49804429 49804429 49804429 CTGGACTGGGACTCTGGCTTCTCGGAGGTGTCAGGCAGCACATGGCGAGAGGAAGAACTGCCTGT CTGGACTGGGACTCTGGCTTCTCGGAGGTGTCGGGCAGCACATGGCGAGAGGAAGAACTGCCTGT A G INKA1 Ensembl:ENSG00000185614 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49804283..49804569 26863196 MeRIP-seq:(Medium) rs994314840 Functional Loss SNV dbSNP153 33..33 33 - - - 87336 RMVar_ID_87336 Human_SNP_ID_132618968 m1A Human chr3 + 49807998 49807998 49807998 AGGGCCAGGGTTTGCCCTCCACCTCCAGGCCCAAGCCTCAAGGGGTGGGGTTACCTGGGCACGGT AGGGCCAGGGTTTGCCCTCCACCTCCAGGCCCCAGCCTCAAGGGGTGGGGTTACCTGGGCACGGT A C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:49807900..49808013 26863196 MeRIP-seq:(Medium) rs2234388 Functional Loss SNV dbSNP153 33..33 33 - - - 87337 RMVar_ID_87337 Human_SNP_ID_132642946 m1A Human chr3 + 49903490 49903490 49903490 GCGGAGAAGCTGGGCACCACGTACTTCACGTCAAAGTCGCGAGAGGCCGCGTAGGGGGTGCGCGG GCGGAGAAGCTGGGCACCACGTACTTCACGTCCAAGTCGCGAGAGGCCGCGTAGGGGGTGCGCGG A C AC105935.2 Ensembl:ENSG00000230698 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49903446..49903833 26863196 MeRIP-seq:(Medium) rs570923795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_431706 87338 RMVar_ID_87338 Human_SNP_ID_132642947 m1A Human chr3 + 49903490 49903490 49903490 GCGGAGAAGCTGGGCACCACGTACTTCACGTCAAAGTCGCGAGAGGCCGCGTAGGGGGTGCGCGG GCGGAGAAGCTGGGCACCACGTACTTCACGTCGAAGTCGCGAGAGGCCGCGTAGGGGGTGCGCGG A G AC105935.2 Ensembl:ENSG00000230698 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49903446..49903833 26863196 MeRIP-seq:(Medium) rs570923795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_431706 87339 RMVar_ID_87339 Human_SNP_ID_132643001 m1A Human chr3 + 49903602 49903602 49903602 GCAACAGGAAGGACTGAGGCAGCGGCGGGAGGAGCTCCATCGAGGCGAGCTGGGACCCTAGAGGA GCAACAGGAAGGACTGAGGCAGCGGCGGGAGGCGCTCCATCGAGGCGAGCTGGGACCCTAGAGGA A C AC105935.2 Ensembl:ENSG00000230698 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:49903554..49903846;chr3:49903406..49903849 26863196 MeRIP-seq:(Medium) rs1352914420 Functional Loss SNV dbSNP153 33..33 33 - - - 87340 RMVar_ID_87340 Human_SNP_ID_132644242 m1A Human chr3 - 49909106 49909106 49909106 AGCTCTACATGTGTTACAGCCCCCTGGGGACCAAGGCGTCAGCCGTCAGTGCCATCCATAAGCTG AGCTCTACATGTGTTACAGCCCCCTGGGGACCGAGGCGTCAGCCGTCAGTGCCATCCATAAGCTG T C MON1A Ensembl:ENSG00000164077 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49909060..49909260 26863196 MeRIP-seq:(Medium) rs902338992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_431724,Human_Splice_Rec_431734,Human_Splice_Rec_431744,Human_Splice_Rec_431752,Human_Splice_Rec_431764 87341 RMVar_ID_87341 Human_SNP_ID_132644321 m1A Human chr3 - 49909297 49909297 49909297 ACAGTCGTGCCCACAATGCCTCTCGCCCACTCAAGACCATTTACTACACGGGCCCCAACGAGAAC ACAGTCGTGCCCACAATGCCTCTCGCCCACTCGAGACCATTTACTACACGGGCCCCAACGAGAAC T C MON1A Ensembl:ENSG00000164077 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:49909157..49909296 26863196 MeRIP-seq:(Medium) rs1384425206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27503209 Human_Splice_Rec_431723,Human_Splice_Rec_431733,Human_Splice_Rec_431743,Human_Splice_Rec_431751,Human_Splice_Rec_431763 RMVar_hsa_circ_16371 87342 RMVar_ID_87342 Human_SNP_ID_132644571 m1A Human chr3 - 49910354 49910352 49910354 AATTCAACGCAGCCGGCTTCTTCCACGCACACATCTCTTACCTAGAGCCTGACACTGACCTCTGC AATTCAACGCAGCCGGCTTCTTCCACGCACAC__CTCTTACCTAGAGCCTGACACTGACCTCTGC GAT G MON1A Ensembl:ENSG00000164077 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49910305..49910406 32194978 MeRIP-seq:(Medium) rs756790800 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14872248,Human_RBP_ID_27503212 RMVar_hsa_circ_16371 87343 RMVar_ID_87343 Human_SNP_ID_132644733 m1A Human chr3 + 49910695 49910695 49910695 GCAGGTTGTCGGTGATGCGCTCTGAGCCCGAGAGTAGGCGCCGCAAATCATAGTTCTGCTTCTGC GCAGGTTGTCGGTGATGCGCTCTGAGCCCGAGCGTAGGCGCCGCAAATCATAGTTCTGCTTCTGC A C AC105935.1 Ensembl:ENSG00000228008 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49910653..49910754 32194978 MeRIP-seq:(Medium) rs1455643711 Functional Loss SNV dbSNP153 33..33 33 - - - 87344 RMVar_ID_87344 Human_SNP_ID_132645187 m1A Human chr3 - 49911773 49911773 49911773 ATGCTGCCAGGAAGCTCTGAGGATTGGCTGGAACCCCCAGGGGCAGTTGGGCGACCAGCCACAGA ATGCTGCCAGGAAGCTCTGAGGATTGGCTGGAGCCCCCAGGGGCAGTTGGGCGACCAGCCACAGA T C MON1A Ensembl:ENSG00000164077 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49911722..49911993 26863196 MeRIP-seq:(Medium) rs1377369951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16371 87345 RMVar_ID_87345 Human_SNP_ID_132645191 m1A Human chr3 + 49911781 49911781 49911781 TGGTCGCCCAACTGCCCCTGGGGGTTCCAGCCAATCCTCAGAGCTTCCTGGCAGCATCTCCTCCT TGGTCGCCCAACTGCCCCTGGGGGTTCCAGCCGATCCTCAGAGCTTCCTGGCAGCATCTCCTCCT A G AC105935.1 Ensembl:ENSG00000228008 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49911730..49911944 26863196 MeRIP-seq:(Medium) rs1338966725 Functional Loss SNV dbSNP153 33..33 33 - - - 87346 RMVar_ID_87346 Human_SNP_ID_132658160 m1A Human chr3 + 49962638 49962637 49962639 AGGATTTACTTGTTGGGGCCCTCTTGATAAAAAGAGATGTGGGGGGATTCTCGACCTGCTAACAG AGGATTTACTTGTTGGGGCCCTCTTGATAAAA__AGATGTGGGGGGATTCTCGACCTGCTAACAG AAG A RBM6 Ensembl:ENSG00000004534 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49962530..49962650 26863196 MeRIP-seq:(Medium) rs1262514360 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1069175,Human_RBP_ID_2789452,Human_RBP_ID_4766278,Human_RBP_ID_5530466,Human_RBP_ID_8235921,Human_RBP_ID_8575148,Human_RBP_ID_18007539,Human_RBP_ID_18182142,Human_RBP_ID_18423985,Human_RBP_ID_18810714,Human_RBP_ID_19115575,Human_RBP_ID_22608162,Human_RBP_ID_23026511,Human_RBP_ID_27822265 Human_Splice_Rec_431780,Human_Splice_Rec_431781,Human_Splice_Rec_431812,Human_Splice_Rec_431813,Human_Splice_Rec_431852,Human_Splice_Rec_431853,Human_Splice_Rec_431882,Human_Splice_Rec_431883,Human_Splice_Rec_431914,Human_Splice_Rec_431916,Human_Splice_Rec_431917,Human_Splice_Rec_431952,Human_Splice_Rec_431953,Human_Splice_Rec_431990,Human_Splice_Rec_431991,Human_Splice_Rec_432030,Human_Splice_Rec_432031,Human_Splice_Rec_432044,Human_Splice_Rec_432045,Human_Splice_Rec_432084,Human_Splice_Rec_432085,Human_Splice_Rec_432088,Human_Splice_Rec_432089,Human_Splice_Rec_432091 RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_367482,RMVar_hsa_circ_368196,RMVar_hsa_circ_361486,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_218305 87347 RMVar_ID_87347 Human_SNP_ID_132658167 m1A Human chr3 + 49962659 49962659 49962659 TCTTGATAAAAAGAGATGTGGGGGGATTCTCGACCTGCTAACAGAACTGGACCTTTTCGGTAAGT TCTTGATAAAAAGAGATGTGGGGGGATTCTCGTCCTGCTAACAGAACTGGACCTTTTCGGTAAGT A T RBM6 Ensembl:ENSG00000004534 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:49962539..49962732;chr3:49962527..49962732 26863196 MeRIP-seq:(Medium) rs914800697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66263,Human_RBP_ID_1069175,Human_RBP_ID_1964765,Human_RBP_ID_5530466,Human_RBP_ID_8235921,Human_RBP_ID_14872527,Human_RBP_ID_18423985,Human_RBP_ID_18810714,Human_RBP_ID_19012338,Human_RBP_ID_19115575,Human_RBP_ID_22608162,Human_RBP_ID_23026511 Human_Splice_Rec_431780,Human_Splice_Rec_431781,Human_Splice_Rec_431812,Human_Splice_Rec_431813,Human_Splice_Rec_431852,Human_Splice_Rec_431853,Human_Splice_Rec_431882,Human_Splice_Rec_431883,Human_Splice_Rec_431914,Human_Splice_Rec_431916,Human_Splice_Rec_431917,Human_Splice_Rec_431952,Human_Splice_Rec_431953,Human_Splice_Rec_431990,Human_Splice_Rec_431991,Human_Splice_Rec_432030,Human_Splice_Rec_432031,Human_Splice_Rec_432044,Human_Splice_Rec_432045,Human_Splice_Rec_432084,Human_Splice_Rec_432085,Human_Splice_Rec_432088,Human_Splice_Rec_432089,Human_Splice_Rec_432091 RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_367482,RMVar_hsa_circ_368196,RMVar_hsa_circ_361486,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_218305 87348 RMVar_ID_87348 Human_SNP_ID_132659344 m1A Human chr3 - 49967853 49967853 49967853 TCATATGAGGTGCCTCCCTACCTCTATAATCCATAGAAGTACCATCTCCACCCCTATAGTCCATA TCATATGAGGTGCCTCCCTACCTCTATAATCCGTAGAAGTACCATCTCCACCCCTATAGTCCATA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49967601..49968263 26863196 MeRIP-seq:(Medium) rs773500078 Functional Loss SNV dbSNP153 33..33 33 - - - 87349 RMVar_ID_87349 Human_SNP_ID_132689897 m1A Human chr3 + 50090448 50090448 50090448 CTAAATCTTCAGTGGGACAATGGGTTCAGACAAAAGGTAAGTTACTACAGTACGTGGCTTTGATC CTAAATCTTCAGTGGGACAATGGGTTCAGACAGAAGGTAAGTTACTACAGTACGTGGCTTTGATC A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50090348..50090500 26863196 MeRIP-seq:(Medium) rs755910328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834356,Human_RBP_ID_1628813,Human_RBP_ID_4757247,Human_RBP_ID_15001232 Human_Splice_Rec_432076,Human_Splice_Rec_432077,Human_Splice_Rec_432144,Human_Splice_Rec_432145,Human_Splice_Rec_432152,Human_Splice_Rec_432153,Human_Splice_Rec_432164,Human_Splice_Rec_432165,Human_Splice_Rec_432212,Human_Splice_Rec_432213,Human_Splice_Rec_432220,Human_Splice_Rec_432221,Human_Splice_Rec_432228,Human_Splice_Rec_432229,Human_Splice_Rec_432238,Human_Splice_Rec_432239,Human_Splice_Rec_432284,Human_Splice_Rec_432285,Human_Splice_Rec_432290,Human_Splice_Rec_432291,Human_Splice_Rec_432295 RMVar_hsa_circ_37410,RMVar_hsa_circ_87115,RMVar_hsa_circ_218326,RMVar_hsa_circ_35608,RMVar_hsa_circ_218340,RMVar_hsa_circ_122540,RMVar_hsa_circ_86531,RMVar_hsa_circ_114466,RMVar_hsa_circ_353577,RMVar_hsa_circ_218339,RMVar_hsa_circ_356020,RMVar_hsa_circ_269516,RMVar_hsa_circ_57491,RMVar_hsa_circ_218341,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342 87350 RMVar_ID_87350 Human_SNP_ID_132690248 m1A Human chr3 + 50092156 50092156 50092156 GCGGAGGGACTCAGATTACAAAAGATCTAGTGATGATCGGAGGGGTGATAGATATGATGACTACC GCGGAGGGACTCAGATTACAAAAGATCTAGTGGTGATCGGAGGGGTGATAGATATGATGACTACC A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50092106..50092249 26863196 MeRIP-seq:(Medium) rs573048408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628818,Human_RBP_ID_1964935,Human_RBP_ID_2789729,Human_RBP_ID_3710722,Human_RBP_ID_5206124,Human_RBP_ID_7206130,Human_RBP_ID_14875797,Human_RBP_ID_24008846,Human_RBP_ID_26346945 Human_Splice_Rec_432079,Human_Splice_Rec_432147,Human_Splice_Rec_432155,Human_Splice_Rec_432167,Human_Splice_Rec_432215,Human_Splice_Rec_432223,Human_Splice_Rec_432231,Human_Splice_Rec_432241,Human_Splice_Rec_432287,Human_Splice_Rec_432293,Human_Splice_Rec_432297 RMVar_hsa_circ_37410,RMVar_hsa_circ_87115,RMVar_hsa_circ_218326,RMVar_hsa_circ_48362,RMVar_hsa_circ_35608,RMVar_hsa_circ_218340,RMVar_hsa_circ_122540,RMVar_hsa_circ_86531,RMVar_hsa_circ_114466,RMVar_hsa_circ_353577,RMVar_hsa_circ_218339,RMVar_hsa_circ_356020,RMVar_hsa_circ_269516,RMVar_hsa_circ_57491,RMVar_hsa_circ_96641,RMVar_hsa_circ_218341,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_346293,RMVar_hsa_circ_93262,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346 87351 RMVar_ID_87351 Human_SNP_ID_132690711 m1A Human chr3 - 50093678 50093677 50093678 AATAAACAAAATCACAATTAACATCACCCTGTACTCTTTGAAACAGACCCTCCACTCCTAGAAAT AATAAACAAAATCACAATTAACATCACCCTGT_CTCTTTGAAACAGACCCTCCACTCCTAGAAAT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50093675..50093809 26863196 MeRIP-seq:(Medium) rs759558165 Functional Loss DEL dbSNP153 33..33 33 - - - 87352 RMVar_ID_87352 Human_SNP_ID_132690758 m1A Human chr3 - 50093785 50093785 50093785 TCGTCACTGATGTCATGCCTATAGTCGTGCTCACCATAGTCACCATCTGAATGGTAGCCATCTTC TCGTCACTGATGTCATGCCTATAGTCGTGCTCCCCATAGTCACCATCTGAATGGTAGCCATCTTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50090389..50100045 32194978 MeRIP-seq:(Medium) rs769341522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5206132 87353 RMVar_ID_87353 Human_SNP_ID_132695582 m1A Human chr3 + 50112949 50112949 50112949 ATCTTGGCTCACTGCCACCTCCTCCATCTCCCAGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTG ATCTTGGCTCACTGCCACCTCCTCCATCTCCCGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTG A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1303146978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8277,RMVar_hsa_circ_92660,RMVar_hsa_circ_218352,RMVar_hsa_circ_61152,RMVar_hsa_circ_10258,RMVar_hsa_circ_60753,RMVar_hsa_circ_116714,RMVar_hsa_circ_218361,RMVar_hsa_circ_299080,RMVar_hsa_circ_106827,RMVar_hsa_circ_218367,RMVar_hsa_circ_113922,RMVar_hsa_circ_125560,RMVar_hsa_circ_96541,RMVar_hsa_circ_103720,RMVar_hsa_circ_81917,RMVar_hsa_circ_218368,RMVar_hsa_circ_218372,RMVar_hsa_circ_218373,RMVar_hsa_circ_218370,RMVar_hsa_circ_218371,RMVar_hsa_circ_218369,RMVar_hsa_circ_104630,RMVar_hsa_circ_218380,RMVar_hsa_circ_102706,RMVar_hsa_circ_107169,RMVar_hsa_circ_218383,RMVar_hsa_circ_218384 87354 RMVar_ID_87354 Human_SNP_ID_132696949 m1A Human chr3 - 50118444 50118444 50118444 TCTCTCTCTCTCTCTCTCTCTCACTCCATCTCAGTGAACCGGGCAAACATGGCTTTCCGGACAGC TCTCTCTCTCTCTCTCTCTCTCACTCCATCTCTGTGAACCGGGCAAACATGGCTTTCCGGACAGC T A SEMA3F-AS1 Ensembl:ENSG00000235016 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:50118330..50118728;chr3:50118394..50118625 26863196 MeRIP-seq:(Medium) rs778418794 Functional Loss SNV dbSNP153 33..33 33 - - - 87355 RMVar_ID_87355 Human_SNP_ID_132710664 m1A Human chr3 + 50173826 50173826 50173826 GCTGAAGGCCACAGGCACCGCCCACTTCTTCAACTTCCTGCTCAACACAACCGACTACCGAATCT GCTGAAGGCCACAGGCACCGCCCACTTCTTCAGCTTCCTGCTCAACACAACCGACTACCGAATCT A G SEMA3F Ensembl:ENSG00000001617 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:50173776..50173825 26863196 MeRIP-seq:(Medium) rs778564860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9395088,Human_RBP_ID_20786839 Human_Splice_Rec_432428,Human_Splice_Rec_432442,Human_Splice_Rec_432462,Human_Splice_Rec_432496,Human_Splice_Rec_432532,Human_Splice_Rec_432536 RMVar_hsa_circ_83785,RMVar_hsa_circ_218396,RMVar_hsa_circ_78858,RMVar_hsa_circ_218393,RMVar_hsa_circ_293787,RMVar_hsa_circ_371838,RMVar_hsa_circ_218394,RMVar_hsa_circ_304753,RMVar_hsa_circ_218397,RMVar_hsa_circ_218395 87356 RMVar_ID_87356 Human_SNP_ID_132710709 m1A Human chr3 - 50173952 50173952 50173952 CCCCACGTCCCACATCAGGGCCAGCCCTTACAATGAGGGGCTCGCGGTTGATGTCGTGCAGGTCC CCCCACGTCCCACATCAGGGCCAGCCCTTACACTGAGGGGCTCGCGGTTGATGTCGTGCAGGTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50173937..50174050 26863196 MeRIP-seq:(Medium) rs775729500 Functional Loss SNV dbSNP153 33..33 33 - - - 87357 RMVar_ID_87357 Human_SNP_ID_132724758 m1A Human chr3 - 50227178 50227178 50227178 AGCCGCCATCGGCTTACCCTCAGAACGTCCCCAGTGACACCCGCCTTTCTGCTTCGTCCAGCCTA AGCCGCCATCGGCTTACCCTCAGAACGTCCCCGGTGACACCCGCCTTTCTGCTTCGTCCAGCCTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50227054..50229113 26863196 MeRIP-seq:(Medium) rs1232517267 Functional Loss SNV dbSNP153 33..33 33 - - - 87358 RMVar_ID_87358 Human_SNP_ID_132726983 m1A Human chr3 - 50236337 50236337 50236337 CCGCCTTGTCCTCGGCGCTCACGGTGCAGCCCATCCCGCCGTCCGCCGGCCCGGCCGCCGCCCGG CCGCCTTGTCCTCGGCGCTCACGGTGCAGCCCCTCCCGCCGTCCGCCGGCCCGGCCGCCGCCCGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:50236201..50236475 26863196 MeRIP-seq:(Medium) rs782410056 Functional Loss SNV dbSNP153 33..33 33 - - - 87359 RMVar_ID_87359 Human_SNP_ID_132728415 m1A Human chr3 + 50242874 50242874 50242874 GGGGGCTCCAAGGCTGCTGACAGCCTCAGGATATGCAAAGGAGGTGATGGCAGCACCTACTGTGT GGGGGCTCCAAGGCTGCTGACAGCCTCAGGATGTGCAAAGGAGGTGATGGCAGCACCTACTGTGT A G GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50242872..50243072 26863196 MeRIP-seq:(Medium) rs1290458498 Functional Loss SNV dbSNP153 33..33 33 - - - 87360 RMVar_ID_87360 Human_SNP_ID_132730507 m1A Human chr3 + 50252362 50252362 50252362 GCCCCAGGCAGCCGTGGGAACTCCCAGTGCCCAGGGGACACTAACCTTCCTGGTCCCTGGCTATC GCCCCAGGCAGCCGTGGGAACTCCCAGTGCCCGGGGGACACTAACCTTCCTGGTCCCTGGCTATC A G GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50252359..50252550 26863196 MeRIP-seq:(Medium) rs1303786652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22551595 RMVar_hsa_circ_127577,RMVar_hsa_circ_117551,RMVar_hsa_circ_308775,RMVar_hsa_circ_218410,RMVar_hsa_circ_327248,RMVar_hsa_circ_304563,RMVar_hsa_circ_218412,RMVar_hsa_circ_218414,RMVar_hsa_circ_84841,RMVar_hsa_circ_218415,RMVar_hsa_circ_218413,RMVar_hsa_circ_218411 87361 RMVar_ID_87361 Human_SNP_ID_132731437 m1A Human chr3 + 50256177 50256176 50256177 GAAGCCCCATGCTGGCCCCCACTGACCCTCCCACCCCCCATCCCCAGCTACCTGAACGACCTGGA GAAGCCCCATGCTGGCCCCCACTGACCCTCCC_CCCCCCATCCCCAGCTACCTGAACGACCTGGA CA C GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50256176..50256200 32194978 MeRIP-seq:(Medium) rs1553703128 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127577,RMVar_hsa_circ_327248,RMVar_hsa_circ_218412,RMVar_hsa_circ_84841,RMVar_hsa_circ_218413,RMVar_hsa_circ_218411 87362 RMVar_ID_87362 Human_SNP_ID_132731438 m1A Human chr3 + 50256177 50256177 50256177 GAAGCCCCATGCTGGCCCCCACTGACCCTCCCACCCCCCATCCCCAGCTACCTGAACGACCTGGA GAAGCCCCATGCTGGCCCCCACTGACCCTCCCCCCCCCCATCCCCAGCTACCTGAACGACCTGGA A C GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50256176..50256200 32194978 MeRIP-seq:(Medium) rs782374342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127577,RMVar_hsa_circ_327248,RMVar_hsa_circ_218412,RMVar_hsa_circ_84841,RMVar_hsa_circ_218413,RMVar_hsa_circ_218411 87363 RMVar_ID_87363 Human_SNP_ID_132731816 m1A Human chr3 + 50257560 50257559 50257561 CTACATCCAGAGTAAGTTTGAGGACCTGAATAAGCGCAAAGACACCAAGGAGATCTACACGCACT CTACATCCAGAGTAAGTTTGAGGACCTGAATA__CGCAAAGACACCAAGGAGATCTACACGCACT AAG A GNAI2 Ensembl:ENSG00000114353 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50257511..50257736 26863196 MeRIP-seq:(Medium) rs1553703452 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1628959,Human_RBP_ID_3710813,Human_RBP_ID_18194603,Human_RBP_ID_26823890 Human_Splice_Rec_432738,Human_Splice_Rec_432756,Human_Splice_Rec_432772,Human_Splice_Rec_432788,Human_Splice_Rec_432804,Human_Splice_Rec_432820,Human_Splice_Rec_432834,Human_Splice_Rec_432850,Human_Splice_Rec_432862,Human_Splice_Rec_432872 RMVar_hsa_circ_327248,RMVar_hsa_circ_218411,RMVar_hsa_circ_354790,RMVar_hsa_circ_354757 87364 RMVar_ID_87364 Human_SNP_ID_132731819 m1A Human chr3 + 50257560 50257560 50257560 CTACATCCAGAGTAAGTTTGAGGACCTGAATAAGCGCAAAGACACCAAGGAGATCTACACGCACT CTACATCCAGAGTAAGTTTGAGGACCTGAATACGCGCAAAGACACCAAGGAGATCTACACGCACT A C GNAI2 Ensembl:ENSG00000114353 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50257511..50257736 26863196 MeRIP-seq:(Medium) rs1553703449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628959,Human_RBP_ID_3710813,Human_RBP_ID_18194603,Human_RBP_ID_26823890 Human_Splice_Rec_432738,Human_Splice_Rec_432756,Human_Splice_Rec_432772,Human_Splice_Rec_432788,Human_Splice_Rec_432804,Human_Splice_Rec_432820,Human_Splice_Rec_432834,Human_Splice_Rec_432850,Human_Splice_Rec_432862,Human_Splice_Rec_432872 RMVar_hsa_circ_327248,RMVar_hsa_circ_218411,RMVar_hsa_circ_354790,RMVar_hsa_circ_354757 87365 RMVar_ID_87365 Human_SNP_ID_132731828 m1A Human chr3 + 50257575 50257573 50257576 GTTTGAGGACCTGAATAAGCGCAAAGACACCAAGGAGATCTACACGCACTTCACGTGCGCCACCG GTTTGAGGACCTGAATAAGCGCAAAGACACC___GAGATCTACACGCACTTCACGTGCGCCACCG CAAG C GNAI2 Ensembl:ENSG00000114353 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50257526..50257754 26863196 MeRIP-seq:(Medium) rs1553703463 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18194603,Human_RBP_ID_26823890 Human_Splice_Rec_432738,Human_Splice_Rec_432756,Human_Splice_Rec_432772,Human_Splice_Rec_432788,Human_Splice_Rec_432804,Human_Splice_Rec_432820,Human_Splice_Rec_432834,Human_Splice_Rec_432850,Human_Splice_Rec_432862,Human_Splice_Rec_432872 Human_miRNA_ID_1112247 RMVar_hsa_circ_327248,RMVar_hsa_circ_218411,RMVar_hsa_circ_354790,RMVar_hsa_circ_354757 87366 RMVar_ID_87366 Human_SNP_ID_132731829 m1A Human chr3 + 50257575 50257575 50257575 GTTTGAGGACCTGAATAAGCGCAAAGACACCAAGGAGATCTACACGCACTTCACGTGCGCCACCG GTTTGAGGACCTGAATAAGCGCAAAGACACCACGGAGATCTACACGCACTTCACGTGCGCCACCG A C GNAI2 Ensembl:ENSG00000114353 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50257526..50257754 26863196 MeRIP-seq:(Medium) rs1406706731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18194603,Human_RBP_ID_26823890 Human_Splice_Rec_432738,Human_Splice_Rec_432756,Human_Splice_Rec_432772,Human_Splice_Rec_432788,Human_Splice_Rec_432804,Human_Splice_Rec_432820,Human_Splice_Rec_432834,Human_Splice_Rec_432850,Human_Splice_Rec_432862,Human_Splice_Rec_432872 Human_miRNA_ID_1112247 RMVar_hsa_circ_327248,RMVar_hsa_circ_218411,RMVar_hsa_circ_354790,RMVar_hsa_circ_354757 87367 RMVar_ID_87367 Human_SNP_ID_132732211 m1A Human chr3 + 50258965 50258965 50258965 AGAGAAAAACTATTTAAAACTGTCAGATCCTGACCAGCAAGCCCCCCCCCAGCCCCCCTTCCAAG AGAGAAAAACTATTTAAAACTGTCAGATCCTGTCCAGCAAGCCCCCCCCCAGCCCCCCTTCCAAG A T GNAI2 Ensembl:ENSG00000114353 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:50258926..50259000 26863196 MeRIP-seq:(Medium) rs910480787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604589,Human_RBP_ID_1105473,Human_RBP_ID_5133441,Human_RBP_ID_8209733,Human_RBP_ID_17520360,Human_RBP_ID_17661427,Human_RBP_ID_18954380,Human_RBP_ID_22509704,Human_RBP_ID_26510394,Human_RBP_ID_27503294 Human_miRNA_ID_273353 87368 RMVar_ID_87368 Human_SNP_ID_132733527 m1A Human chr3 - 50264241 50264241 50264241 CTCCTCTCTTGTCCCCTTTTGCTGTGCCCCTCACCCCAGTACTTTTTTTTTTCTTCTTTTTTTTG CTCCTCTCTTGTCCCCTTTTGCTGTGCCCCTCCCCCCAGTACTTTTTTTTTTCTTCTTTTTTTTG T G lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50264234..50264310 26863196 MeRIP-seq:(Medium) rs1222142362 Functional Loss SNV dbSNP153 33..33 33 - - - 87369 RMVar_ID_87369 Human_SNP_ID_132734340 m1A Human chr3 - 50267692 50267691 50267692 CTGCCTTCTCACACTCCACCGAGGACTTCCGCAGCAGCATCTCTCCACTCTGGCCCCTTCCCACC CTGCCTTCTCACACTCCACCGAGGACTTCCGC_GCAGCATCTCTCCACTCTGGCCCCTTCCCACC CT C lnc-HYAL3-1,SEMA3B-AS1 RNACentral:URS00008BE585,RNACentral:URS0000D5A37A lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50267598..50267769 26863196 MeRIP-seq:(Medium) rs1344543573 Functional Loss DEL dbSNP153 33..33 33 - - - 87370 RMVar_ID_87370 Human_SNP_ID_132734699 m1A Human chr3 - 50269229 50269229 50269229 GGCAGCCCCGGCCCGCCCCATCTCAGCAGCTCAGGGTGCTCAGGGTTCAGCGGGTGTGTGTGTGG GGCAGCCCCGGCCCGCCCCATCTCAGCAGCTCGGGGTGCTCAGGGTTCAGCGGGTGTGTGTGTGG T C lnc-HYAL3-1,SEMA3B-AS1 RNACentral:URS00008BE585,RNACentral:URS0000D5A37A lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:50269112..50269378;chr3:50269134..50269337;chr3:50269143..50269371 26863196 MeRIP-seq:(Medium) rs1553704913 Functional Loss SNV dbSNP153 33..33 33 - - - 87371 RMVar_ID_87371 Human_SNP_ID_132735174 m1A Human chr3 + 50270871 50270871 50270871 CCTCTTAAGGCTACGTCCCTGGGGGAAGCCTCACACCTCCAACCCTACTAGACTGAGTGCATGAA CCTCTTAAGGCTACGTCCCTGGGGGAAGCCTCGCACCTCCAACCCTACTAGACTGAGTGCATGAA A G SEMA3B Ensembl:ENSG00000012171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50270867..50270949 26863196 MeRIP-seq:(Medium) rs1553705214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933776,Human_RBP_ID_1069180,Human_RBP_ID_5393123,Human_RBP_ID_18953572,Human_RBP_ID_22551597,Human_RBP_ID_22677248 87372 RMVar_ID_87372 Human_SNP_ID_132735236 m1A Human chr3 + 50271013 50271013 50271013 CCTTTGTGGAAGTGGGCCACCGGGCAGAGGTAAGGCCGGATCTAGGCAGGGAGGGAGGTCAGGAG CCTTTGTGGAAGTGGGCCACCGGGCAGAGGTATGGCCGGATCTAGGCAGGGAGGGAGGTCAGGAG A T SEMA3B Ensembl:ENSG00000012171 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:50271010..50271100 26863196 MeRIP-seq:(Medium) rs782023960 Functional Loss SNV dbSNP153 33..33 33 - - - 87373 RMVar_ID_87373 Human_SNP_ID_132735289 m1A Human chr3 + 50271122 50271122 50271122 GCCCGTCCTCCGGCTGGACCCAGGAAGGATAGAGGATGGCAAGGGGAAGAGTCCTTATGACCCCA GCCCGTCCTCCGGCTGGACCCAGGAAGGATAGGGGATGGCAAGGGGAAGAGTCCTTATGACCCCA A G SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50270993..50271182 26863196 MeRIP-seq:(Medium) rs993504085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5602684,Human_RBP_ID_18014116,Human_RBP_ID_19012394 Human_Splice_Rec_432888,Human_Splice_Rec_432889,Human_Splice_Rec_432898,Human_Splice_Rec_432899,Human_Splice_Rec_432930,Human_Splice_Rec_432931,Human_Splice_Rec_432960,Human_Splice_Rec_432961,Human_Splice_Rec_432990,Human_Splice_Rec_432991,Human_Splice_Rec_433004,Human_Splice_Rec_433005,Human_Splice_Rec_433036,Human_Splice_Rec_433037,Human_Splice_Rec_433062,Human_Splice_Rec_433063 87374 RMVar_ID_87374 Human_SNP_ID_132735972 m1A Human chr3 + 50273433 50273433 50273433 ACTGGGACGCCTGTCCGTGTCCCGCGTTGGCCAGATCTGCCGGGTGAGGAGTCCCTGGGCCACAC ACTGGGACGCCTGTCCGTGTCCCGCGTTGGCCGGATCTGCCGGGTGAGGAGTCCCTGGGCCACAC A G SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50273393..50273493 32194978 MeRIP-seq:(Medium) rs781927780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393695,Human_RBP_ID_19010485,Human_RBP_ID_22455886 Human_Splice_Rec_432903,Human_Splice_Rec_432935,Human_Splice_Rec_432965,Human_Splice_Rec_432995,Human_Splice_Rec_433009,Human_Splice_Rec_433041,Human_Splice_Rec_433067,Human_Splice_Rec_433087,Human_Splice_Rec_433107,Human_Splice_Rec_433111 87375 RMVar_ID_87375 Human_SNP_ID_132736059 m1A Human chr3 + 50273638 50273638 50273638 GGTGCCCGGCGTCGAGGGCGACACCCACTTCGATCAGCTCCGTGAGTGCGGGAGTGGGTATGGGG GGTGCCCGGCGTCGAGGGCGACACCCACTTCGGTCAGCTCCGTGAGTGCGGGAGTGGGTATGGGG A G SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50273587..50273727 26863196 MeRIP-seq:(Medium) rs1307245634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_432905,Human_Splice_Rec_432967,Human_Splice_Rec_433011,Human_Splice_Rec_433043,Human_Splice_Rec_433069,Human_Splice_Rec_433089,Human_Splice_Rec_433109,Human_Splice_Rec_433117,Human_Splice_Rec_433131 87376 RMVar_ID_87376 Human_SNP_ID_132736309 m1A Human chr3 + 50274412 50274412 50274412 TGGCACCTTCAGTTCCACCAAGGACTTCCCAGACGATGTCATCCAGTTTGCGCGGAACCACCCCC TGGCACCTTCAGTTCCACCAAGGACTTCCCAGCCGATGTCATCCAGTTTGCGCGGAACCACCCCC A C SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:50274301..50274475 26863196 MeRIP-seq:(Medium) rs782730338 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9395104 Human_Splice_Rec_432910,Human_Splice_Rec_432940,Human_Splice_Rec_432972,Human_Splice_Rec_433016,Human_Splice_Rec_433048,Human_Splice_Rec_433074,Human_Splice_Rec_433094,Human_Splice_Rec_433110,Human_Splice_Rec_433118,Human_Splice_Rec_433136 Human_miRNA_ID_2721366 RMVar_hsa_circ_96619,RMVar_hsa_circ_218419 87377 RMVar_ID_87377 Human_SNP_ID_132736310 m1A Human chr3 + 50274412 50274412 50274412 TGGCACCTTCAGTTCCACCAAGGACTTCCCAGACGATGTCATCCAGTTTGCGCGGAACCACCCCC TGGCACCTTCAGTTCCACCAAGGACTTCCCAGGCGATGTCATCCAGTTTGCGCGGAACCACCCCC A G SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:50274301..50274475 26863196 MeRIP-seq:(Medium) rs782730338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9395104 Human_Splice_Rec_432910,Human_Splice_Rec_432940,Human_Splice_Rec_432972,Human_Splice_Rec_433016,Human_Splice_Rec_433048,Human_Splice_Rec_433074,Human_Splice_Rec_433094,Human_Splice_Rec_433110,Human_Splice_Rec_433118,Human_Splice_Rec_433136 Human_miRNA_ID_2721366 RMVar_hsa_circ_96619,RMVar_hsa_circ_218419 87378 RMVar_ID_87378 Human_SNP_ID_132736315 m1A Human chr3 + 50274424 50274424 50274424 TTCCACCAAGGACTTCCCAGACGATGTCATCCAGTTTGCGCGGAACCACCCCCTCATGTACAACT TTCCACCAAGGACTTCCCAGACGATGTCATCCGGTTTGCGCGGAACCACCCCCTCATGTACAACT A G SEMA3B Ensembl:ENSG00000012171 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50274373..50274576 26863196 MeRIP-seq:(Medium) rs1553706095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_938566,Human_RBP_ID_9395104 Human_Splice_Rec_432910,Human_Splice_Rec_432940,Human_Splice_Rec_432972,Human_Splice_Rec_433016,Human_Splice_Rec_433048,Human_Splice_Rec_433074,Human_Splice_Rec_433094,Human_Splice_Rec_433110,Human_Splice_Rec_433118,Human_Splice_Rec_433136 RMVar_hsa_circ_96619,RMVar_hsa_circ_218419 87379 RMVar_ID_87379 Human_SNP_ID_132736633 m1A Human chr3 - 50275347 50275347 50275347 GCAGACGCGGCCGTGGGCAGCGCAGCGGTGCAACGCGATCTGGGCCACCGCGCTCCGCGAGGCTA GCAGACGCGGCCGTGGGCAGCGCAGCGGTGCAGCGCGATCTGGGCCACCGCGCTCCGCGAGGCTA T C lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50275211..50275346 26863196 MeRIP-seq:(Medium) rs1553706327 Functional Loss SNV dbSNP153 33..33 33 - - - 87380 RMVar_ID_87380 Human_SNP_ID_132736728 m1A Human chr3 - 50275564 50275564 50275564 GGGGTCGCCATTCCTTACGTCTTGCCGCCGGAACCGCCTGTGGGGAACATCCGATCTTCTGTGAG GGGGTCGCCATTCCTTACGTCTTGCCGCCGGACCCGCCTGTGGGGAACATCCGATCTTCTGTGAG T G lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50275268..50275707 32194978 MeRIP-seq:(Medium) rs1553706431 Functional Loss SNV dbSNP153 33..33 33 - - - 87381 RMVar_ID_87381 Human_SNP_ID_132736858 m1A Human chr3 - 50275846 50275844 50275846 AGGAGCCTGGCGGGGAGGGCGGAGTAAGGCTCACCTGGGTGTGGGCTGTCACCCCTGCGCGCTGG AGGAGCCTGGCGGGGAGGGCGGAGTAAGGCTC__CTGGGTGTGGGCTGTCACCCCTGCGCGCTGG GGT G lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50275826..50275850 26863196 MeRIP-seq:(Medium) rs782687219 Functional Loss DEL dbSNP153 33..34 33 - - - 87382 RMVar_ID_87382 Human_SNP_ID_132736860 m1A Human chr3 - 50275846 50275846 50275846 AGGAGCCTGGCGGGGAGGGCGGAGTAAGGCTCACCTGGGTGTGGGCTGTCACCCCTGCGCGCTGG AGGAGCCTGGCGGGGAGGGCGGAGTAAGGCTCCCCTGGGTGTGGGCTGTCACCCCTGCGCGCTGG T G lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50275826..50275850 26863196 MeRIP-seq:(Medium) rs1380579581 Functional Loss SNV dbSNP153 33..33 33 - - - 87383 RMVar_ID_87383 Human_SNP_ID_132740421 m1A Human chr3 - 50288168 50288168 50288168 CATCCTGTGAAGCAGGACCTGCTGAAGAGGAGACTTTCTATGCCCTTGGTCCGTATTTTTAACAG CATCCTGTGAAGCAGGACCTGCTGAAGAGGAGGCTTTCTATGCCCTTGGTCCGTATTTTTAACAG T C IFRD2 Ensembl:ENSG00000214706 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50287998..50288209 26863196 MeRIP-seq:(Medium) rs1175290540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604630,Human_RBP_ID_1628976,Human_RBP_ID_4747537,Human_RBP_ID_7206461,Human_RBP_ID_14877357,Human_RBP_ID_18007643,Human_RBP_ID_22509707,Human_RBP_ID_26510398,Human_RBP_ID_27503315 87384 RMVar_ID_87384 Human_SNP_ID_132741362 m1A Human chr3 + 50290256 50290256 50290256 AGAAGTCGGGGAGTAGGCGGGACGCTAGGGCCAGGCGCAGGCTCTCAAGAGCACCCTGCCGGGTC AGAAGTCGGGGAGTAGGCGGGACGCTAGGGCCGGGCGCAGGCTCTCAAGAGCACCCTGCCGGGTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:50290151..50290304 26863196 MeRIP-seq:(Medium) rs374859692 Functional Loss SNV dbSNP153 33..33 33 - - - 87385 RMVar_ID_87385 Human_SNP_ID_132741368 m1A Human chr3 + 50290270 50290270 50290270 AGGCGGGACGCTAGGGCCAGGCGCAGGCTCTCAAGAGCACCCTGCCGGGTCTTGGCACTGGGGGA AGGCGGGACGCTAGGGCCAGGCGCAGGCTCTCCAGAGCACCCTGCCGGGTCTTGGCACTGGGGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50290219..50290700 26863196 MeRIP-seq:(Medium) rs1553709561 Functional Loss SNV dbSNP153 33..33 33 - - - 87386 RMVar_ID_87386 Human_SNP_ID_132741537 m1A Human chr3 - 50290573 50290573 50290573 AGTGAATGCCCCAGCCTTCTCAGCACCACTGCAGAGGACAGCCTTGGTGAGAGCGGGTGGAAGTT AGTGAATGCCCCAGCCTTCTCAGCACCACTGCGGAGGACAGCCTTGGTGAGAGCGGGTGGAAGTT T C IFRD2 Ensembl:ENSG00000214706 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50289991..50290708 26863196 MeRIP-seq:(Medium) rs782155853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247988,Human_RBP_ID_604658,Human_RBP_ID_836337,Human_RBP_ID_3964081,Human_RBP_ID_9393701,Human_RBP_ID_26511160 Human_Splice_Rec_433173,Human_Splice_Rec_433205,Human_Splice_Rec_433227,Human_Splice_Rec_433277,Human_Splice_Rec_433301,Human_Splice_Rec_433311 RMVar_hsa_circ_4582,RMVar_hsa_circ_87051,RMVar_hsa_circ_19795,RMVar_hsa_circ_45035,RMVar_hsa_circ_218420 87387 RMVar_ID_87387 Human_SNP_ID_132742005 m1A Human chr3 + 50292206 50292206 50292206 CCCGCCGCTCATACAGCTGTCCCGCGCCCCCCACCCCACTCACCTCCTCCACGGCGCTGACCACC CCCGCCGCTCATACAGCTGTCCCGCGCCCCCCCCCCCACTCACCTCCTCCACGGCGCTGACCACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50292196..50292425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 87388 RMVar_ID_87388 Human_SNP_ID_132742037 m1A Human chr3 + 50292260 50292260 50292260 CGCTGACCACCCTTCCGGAGCGTGTTGCCCTTACGGGCGCGAGGCATGCCGGGAACCGGGCGCGG CGCTGACCACCCTTCCGGAGCGTGTTGCCCTTCCGGGCGCGAGGCATGCCGGGAACCGGGCGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50292170..50292425 26863196 MeRIP-seq:(Medium) rs587703638 Functional Loss SNV dbSNP153 33..33 33 - - - 87389 RMVar_ID_87389 Human_SNP_ID_132743373 m1A Human chr3 - 50295882 50295882 50295882 TTGTGGGAGGACACAGTGGTGTATTGACAAAGACGGAACATGGGAGGGAATGTACCCTCAGCTCA TTGTGGGAGGACACAGTGGTGTATTGACAAAGGCGGAACATGGGAGGGAATGTACCCTCAGCTCA T C HYAL3 Ensembl:ENSG00000186792 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50295880..50295977 26863196 MeRIP-seq:(Medium) rs1224813934 Functional Loss SNV dbSNP153 33..33 33 - - - 87390 RMVar_ID_87390 Human_SNP_ID_132743796 m1A Human chr3 - 50297168 50297168 50297168 CTCCCGCCTGCACTCCCTGGGCCAGTCCTCAGATGCCTTCCCCCTCTGCCTGATGCTGCTAAGCC CTCCCGCCTGCACTCCCTGGGCCAGTCCTCAGGTGCCTTCCCCCTCTGCCTGATGCTGCTAAGCC T C HYAL3,NAA80 Ensembl:ENSG00000186792,Ensembl:ENSG00000243477 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50297147..50297297 26863196 MeRIP-seq:(Medium) rs1329152931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22092383 87391 RMVar_ID_87391 Human_SNP_ID_132743800 m1A Human chr3 - 50297189 50297189 50297189 TCAGTGGCCCCGCAGCCGCACCTCCCGCCTGCACTCCCTGGGCCAGTCCTCAGATGCCTTCCCCC TCAGTGGCCCCGCAGCCGCACCTCCCGCCTGCCCTCCCTGGGCCAGTCCTCAGATGCCTTCCCCC T G HYAL3,NAA80 Ensembl:ENSG00000186792,Ensembl:ENSG00000243477 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50297140..50297336 26863196 MeRIP-seq:(Medium) rs782290237 Functional Loss SNV dbSNP153 33..33 33 - - - 87392 RMVar_ID_87392 Human_SNP_ID_132743817 m1A Human chr3 - 50297234 50297234 50297234 CCGCCGACCCGAGCTCCTGGATGCTTGTGCTGACCTCATCAATGATCAGTGGCCCCGCAGCCGCA CCGCCGACCCGAGCTCCTGGATGCTTGTGCTGTCCTCATCAATGATCAGTGGCCCCGCAGCCGCA T A HYAL3,NAA80 Ensembl:ENSG00000186792,Ensembl:ENSG00000243477 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50297184..50297293 26863196 MeRIP-seq:(Medium) rs1553711463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604669,Human_RBP_ID_22093059,Human_RBP_ID_24009125 87393 RMVar_ID_87393 Human_SNP_ID_132744181 m1A Human chr3 - 50298680 50298679 50298680 GGAGGCCCCCTCTGGAGCAGGTGAGTAGAAGGAGGGGGCTCAGCTGCCCGCCCACGACTAGAAAA GGAGGCCCCCTCTGGAGCAGGTGAGTAGAAGG_GGGGGCTCAGCTGCCCGCCCACGACTAGAAAA CT C HYAL3,NAA80 Ensembl:ENSG00000186792,Ensembl:ENSG00000243477 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50298677..50298829 26863196 MeRIP-seq:(Medium) rs1408859370 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9334194 87394 RMVar_ID_87394 Human_SNP_ID_132744375 m1A Human chr3 - 50299352 50299352 50299352 CTGGGAGGCCTTAGAACGCCGTGGCGTGCCGCAGGACGCGACGGCTGCAGAACATCCGCCGCACC CTGGGAGGCCTTAGAACGCCGTGGCGTGCCGCCGGACGCGACGGCTGCAGAACATCCGCCGCACC T G HYAL3,NAA80 Ensembl:ENSG00000186792,Ensembl:ENSG00000243477 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50299066..50299371 26863196 MeRIP-seq:(Medium) rs1559813859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757250 87395 RMVar_ID_87395 Human_SNP_ID_132750475 m1A Human chr3 - 50318445 50318445 50318445 GTCCTGGGCCACCCAATATTGCAGCCGGGCCCAGTGCCATGGCCATGGGCGCTGTGTGCGCCGCA GTCCTGGGCCACCCAATATTGCAGCCGGGCCCCGTGCCATGGCCATGGGCGCTGTGTGCGCCGCA T G HYAL2 Ensembl:ENSG00000068001 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50318401..50318475 32194978 MeRIP-seq:(Medium) rs1474381196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834951,Human_RBP_ID_17661130,Human_RBP_ID_18014118,Human_RBP_ID_22455904 Human_Splice_Rec_433412,Human_Splice_Rec_433418,Human_Splice_Rec_433424,Human_Splice_Rec_433432 87396 RMVar_ID_87396 Human_SNP_ID_132750911 m1A Human chr3 + 50319709 50319709 50319709 ACGGAAGCTCACAAAGTTGCGGCCATGGCGGGAGGAAGCAAGTGTCTCGTCCAGGTAGACAGACG ACGGAAGCTCACAAAGTTGCGGCCATGGCGGGCGGAAGCAAGTGTCTCGTCCAGGTAGACAGACG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:50319659..50319810;chr3:50319659..50320174 32194978 MeRIP-seq:(Medium) rs1050073 Functional Loss SNV dbSNP153 33..33 33 - - - 87397 RMVar_ID_87397 Human_SNP_ID_132750912 m1A Human chr3 + 50319709 50319709 50319709 ACGGAAGCTCACAAAGTTGCGGCCATGGCGGGAGGAAGCAAGTGTCTCGTCCAGGTAGACAGACG ACGGAAGCTCACAAAGTTGCGGCCATGGCGGGGGGAAGCAAGTGTCTCGTCCAGGTAGACAGACG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:50319659..50319810;chr3:50319659..50320174 32194978 MeRIP-seq:(Medium) rs1050073 Functional Loss SNV dbSNP153 33..33 33 - - - 87398 RMVar_ID_87398 Human_SNP_ID_132751034 m1A Human chr3 - 50319960 50319960 50319960 GCCTCCAGACCGCATAGTCAAACAGGCACAATATGAGTTTGAGTTCGCAGCACAGCAGTTCATGC GCCTCCAGACCGCATAGTCAAACAGGCACAATGTGAGTTTGAGTTCGCAGCACAGCAGTTCATGC T C HYAL2 Ensembl:ENSG00000068001 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50319909..50320010 32194978 MeRIP-seq:(Medium) rs1553716316 Functional Loss SNV dbSNP153 33..33 33 - - - 87399 RMVar_ID_87399 Human_SNP_ID_132751238 m1A Human chr3 - 50320475 50320475 50320475 CCTCCTGCAGCCCCCAGCATGCGGGCAGGCCCAGGCCCCACCGTTACATTGGCCCTGGTGCTGGC CCTCCTGCAGCCCCCAGCATGCGGGCAGGCCCGGGCCCCACCGTTACATTGGCCCTGGTGCTGGC T C HYAL2,TUSC2 Ensembl:ENSG00000068001,Ensembl:ENSG00000114383 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50320426..50324938 26863196 MeRIP-seq:(Medium) rs1408518132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604683,Human_RBP_ID_4756494,Human_RBP_ID_22455907 Human_Splice_Rec_433414,Human_Splice_Rec_433420,Human_Splice_Rec_433428,Human_Splice_Rec_433434,Human_Splice_Rec_433438,Human_Splice_Rec_433440,Human_Splice_Rec_433442,Human_Splice_Rec_433446,Human_Splice_Rec_433448,Human_Splice_Rec_433452 87400 RMVar_ID_87400 Human_SNP_ID_132753251 m1A Human chr3 + 50328151 50328151 50328151 GGCGGGCCCCGTGGCCGCTCTGCTCACACCGCAGTCCGCACTACCATAACCTGCCCCAGCCGCTG GGCGGGCCCCGTGGCCGCTCTGCTCACACCGCGGTCCGCACTACCATAACCTGCCCCAGCCGCTG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr3:50328054..50328153 26863410 MeRIP-seq:(Medium) rs1013356687 Functional Loss SNV dbSNP153 33..33 33 - - - 87401 RMVar_ID_87401 Human_SNP_ID_132753266 m1A Human chr3 - 50328170 50328170 50328170 CGGCGGCGGCACCTGCGATCAGCGGCTGGGGCAGGTTATGGTAGTGCGGACTGCGGTGTGAGCAG CGGCGGCGGCACCTGCGATCAGCGGCTGGGGCGGGTTATGGTAGTGCGGACTGCGGTGTGAGCAG T C TUSC2 Ensembl:ENSG00000114383 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50327956..50328225 26863196 MeRIP-seq:(Medium) rs1471328467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247170,Human_RBP_ID_783076,Human_RBP_ID_4747757,Human_RBP_ID_18423988,Human_RBP_ID_22509711,Human_RBP_ID_24009168 Human_miRNA_ID_2150708,Human_miRNA_ID_2419198 RMVar_hsa_circ_85102,RMVar_hsa_circ_218425 87402 RMVar_ID_87402 Human_SNP_ID_132753773 m1A Human chr3 - 50329882 50329882 50329882 GTGCGTGAATGTATGTAATGTGTGGTGGCCTCAGCTGAATGCCTCCTGTGGGGAAAGGGGTTGGG GTGCGTGAATGTATGTAATGTGTGGTGGCCTCGGCTGAATGCCTCCTGTGGGGAAAGGGGTTGGG T C RASSF1 Ensembl:ENSG00000068028 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50329831..50329931 32194978 MeRIP-seq:(Medium) rs1001575032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604722,Human_RBP_ID_785089,Human_RBP_ID_1105476,Human_RBP_ID_5120555,Human_RBP_ID_5149720,Human_RBP_ID_5654349,Human_RBP_ID_8575408,Human_RBP_ID_17660880,Human_RBP_ID_18194604,Human_RBP_ID_22481104,Human_RBP_ID_22608186,Human_RBP_ID_23213162,Human_RBP_ID_24009169,Human_RBP_ID_26510402 Human_miRNA_ID_658325 87403 RMVar_ID_87403 Human_SNP_ID_132755718 m1A Human chr3 + 50337318 50337318 50337318 TCATTTCGAAAGAAGGCGCCTCCGCCTCGCCCATAGCCGTACCCGCCCGTCCCCCAGTCCTGCGC TCATTTCGAAAGAAGGCGCCTCCGCCTCGCCCGTAGCCGTACCCGCCCGTCCCCCAGTCCTGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:50337186..50337425;chr3:50337151..50337450;chr3:50336909..50337450 26863196 MeRIP-seq:(Medium) rs1434626010 Functional Loss SNV dbSNP153 33..33 33 - - - 87404 RMVar_ID_87404 Human_SNP_ID_132756661 m1A Human chr3 + 50340467 50340466 50340467 ACGGACCTAGTCCTCGGGAGCTGTCCCCGCCGACCCCCTCTGCCGCGACTTGACCCGCGGCGACT ACGGACCTAGTCCTCGGGAGCTGTCCCCGCCG_CCCCCTCTGCCGCGACTTGACCCGCGGCGACT GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50340458..50340538 26863196 MeRIP-seq:(Medium) rs747932172 Functional Loss DEL dbSNP153 33..33 33 - - - 87405 RMVar_ID_87405 Human_SNP_ID_132756662 m1A Human chr3 + 50340467 50340467 50340467 ACGGACCTAGTCCTCGGGAGCTGTCCCCGCCGACCCCCTCTGCCGCGACTTGACCCGCGGCGACT ACGGACCTAGTCCTCGGGAGCTGTCCCCGCCGCCCCCCTCTGCCGCGACTTGACCCGCGGCGACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50340458..50340538 26863196 MeRIP-seq:(Medium) rs916919483 Functional Loss SNV dbSNP153 33..33 33 - - - 87406 RMVar_ID_87406 Human_SNP_ID_132756766 m1A Human chr3 - 50340694 50340694 50340694 AGCGTGCCAACGCGCTGCGCATCGCGCGGGGCACCGCGTGCAACCCCACACGGCAGCTGGTCCCT AGCGTGCCAACGCGCTGCGCATCGCGCGGGGCGCCGCGTGCAACCCCACACGGCAGCTGGTCCCT T C RASSF1 Ensembl:ENSG00000068028 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50340651..50340812 26863196 MeRIP-seq:(Medium) rs1418003690 Functional Loss SNV dbSNP153 33..33 33 - - - 87407 RMVar_ID_87407 Human_SNP_ID_132758401 m1A Human chr3 + 50345601 50345601 50345601 AGGTCTCCCATATCGAGGCCGGGGTCCGGCGGATCCTGGGCAGCAGCCGGGGTGGGGATGCTGTC AGGTCTCCCATATCGAGGCCGGGGTCCGGCGGGTCCTGGGCAGCAGCCGGGGTGGGGATGCTGTC A G ZMYND10-AS1 Ensembl:ENSG00000235058 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:50345562..50345710;chr3:50345566..50345704 26863196 MeRIP-seq:(Medium) rs1376343411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5606127 Human_Splice_Rec_433544 87408 RMVar_ID_87408 Human_SNP_ID_132759113 m1A Human chr3 + 50348211 50348211 50348211 TAGTGCCAGGGCTCAGGCTGCAGTATAGCTGGAACACATCCCGGAGACTGGCCCTCTTGTGCCCT TAGTGCCAGGGCTCAGGCTGCAGTATAGCTGGGACACATCCCGGAGACTGGCCCTCTTGTGCCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50348109..50348210 32194978 MeRIP-seq:(Medium) rs1460309463 Functional Loss SNV dbSNP153 33..33 33 - - - 87409 RMVar_ID_87409 Human_SNP_ID_132759573 m1A Human chr3 + 50349651 50349651 50349651 CCCCAACTCTGCCTGTCGGTAAACCCAAGCCCATCTCATTGCAGACCTCTAGTGTGGTCAGATAG CCCCAACTCTGCCTGTCGGTAAACCCAAGCCCGTCTCATTGCAGACCTCTAGTGTGGTCAGATAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50349649..50349799 32194978 MeRIP-seq:(Medium) rs1003793255 Functional Loss SNV dbSNP153 33..33 33 - - - 87410 RMVar_ID_87410 Human_SNP_ID_132759721 m1A Human chr3 - 50350200 50350200 50350200 GGTAGAGGGAACAGCATATGCAGAAGCCAGGAAGGAGGTGAGATCATAGCGTATGTTTGGAAACA GGTAGAGGGAACAGCATATGCAGAAGCCAGGAGGGAGGTGAGATCATAGCGTATGTTTGGAAACA T C NPRL2 Ensembl:ENSG00000114388 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50350116..50350329 26863196 MeRIP-seq:(Medium) rs1559858174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76978,RMVar_hsa_circ_218436 87411 RMVar_ID_87411 Human_SNP_ID_132759833 m1A Human chr3 + 50350660 50350660 50350660 ATTCGATGCGGCAGCCGCTGCCCATGGCAATAACCGGGCCCAGGCCCGTAGCTCCTCGTTCCTCG ATTCGATGCGGCAGCCGCTGCCCATGGCAATAGCCGGGCCCAGGCCCGTAGCTCCTCGTTCCTCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50350627..50350706 26863196 MeRIP-seq:(Medium) rs1372306004 Functional Loss SNV dbSNP153 33..33 33 - - - 87412 RMVar_ID_87412 Human_SNP_ID_132759913 m1A Human chr3 - 50350942 50350942 50350942 CGCAGCGCAGATCTGATGCGGTGGTTTCCTCCAAAGAAAGCGGGATACTCCGGGCCCTGCCGCGC CGCAGCGCAGATCTGATGCGGTGGTTTCCTCCGAAGAAAGCGGGATACTCCGGGCCCTGCCGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50350891..50351018 26863196 MeRIP-seq:(Medium) rs1490914573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76978,RMVar_hsa_circ_218436 87413 RMVar_ID_87413 Human_SNP_ID_132759920 m1A Human chr3 - 50350971 50350971 50350971 CTCCACGCTAGGGACTTGCCTGCCTCTGCCGCAGCGCAGATCTGATGCGGTGGTTTCCTCCAAAG CTCCACGCTAGGGACTTGCCTGCCTCTGCCGCGGCGCAGATCTGATGCGGTGGTTTCCTCCAAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50350873..50351020 26863196 MeRIP-seq:(Medium) rs1364868060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76978,RMVar_hsa_circ_218436 87414 RMVar_ID_87414 Human_SNP_ID_132760015 m1A Human chr3 - 50351369 50351369 50351369 CATAGTAGCGTGGGCCAGGATCTCAGGTGCCCACTGTTCACTCCTCACTGGAGAAAAGGCTGCAA CATAGTAGCGTGGGCCAGGATCTCAGGTGCCCGCTGTTCACTCCTCACTGGAGAAAAGGCTGCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50351367..50351502 26863196 MeRIP-seq:(Medium) rs1559859195 Functional Loss SNV dbSNP153 33..33 33 - - - 87415 RMVar_ID_87415 Human_SNP_ID_132761204 m1A Human chr3 + 50355358 50355358 50355358 CTCAAGGTGGTCTGGAGTTACAGCGTCGGGGGAGCTGCCTCGAAGGTGATTAGACTGGATTCTGG CTCAAGGTGGTCTGGAGTTACAGCGTCGGGGGGGCTGCCTCGAAGGTGATTAGACTGGATTCTGG A G CYB561D2,Z84492.2 Ensembl:ENSG00000114395,Ensembl:ENSG00000272104 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50355309..50355493 26863196 MeRIP-seq:(Medium) rs776147967 Functional Loss SNV dbSNP153 33..33 33 - - - 87416 RMVar_ID_87416 Human_SNP_ID_132761218 m1A Human chr3 - 50355388 50355388 50355388 GCTCCCACACCCCCAGGGAAGGGGGCTGCCCCAGAATCCAGTCTAATCACCTTCGAGGCAGCTCC GCTCCCACACCCCCAGGGAAGGGGGCTGCCCCGGAATCCAGTCTAATCACCTTCGAGGCAGCTCC T C TMEM115 Ensembl:ENSG00000126062 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50355337..50355443 26863196 MeRIP-seq:(Medium) rs750592590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604760,Human_RBP_ID_18007702,Human_RBP_ID_27320398 Human_miRNA_ID_2087709 RMVar_hsa_circ_110098,RMVar_hsa_circ_218439 87417 RMVar_ID_87417 Human_SNP_ID_132762060 m1A Human chr3 + 50358662 50358662 50358662 ACGCCACCTAGGAAGCCCAAGGCGCCGTGGATACGGACAGTGAACAGGTAGACCAGGTTGAAGGA ACGCCACCTAGGAAGCCCAAGGCGCCGTGGATGCGGACAGTGAACAGGTAGACCAGGTTGAAGGA A G Z84492.2 Ensembl:ENSG00000272104 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50358611..50359061 32194978 MeRIP-seq:(Medium) rs1430368707 Functional Loss SNV dbSNP153 33..33 33 - - - 87418 RMVar_ID_87418 Human_SNP_ID_132763834 m1A Human chr3 + 50364694 50364694 50364694 GTGCTCAGAGGCGGCGAGAGGCGTGGACGAGGACTTGAGGCTGCGGCCGGGGCGGCAGGCCCAGG GTGCTCAGAGGCGGCGAGAGGCGTGGACGAGGGCTTGAGGCTGCGGCCGGGGCGGCAGGCCCAGG A G Z84492.2 Ensembl:ENSG00000272104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:50364649..50364737 26863196 MeRIP-seq:(Medium) rs1477373385 Functional Loss SNV dbSNP153 33..33 33 - - - 87419 RMVar_ID_87419 Human_SNP_ID_132815866 m1A Human chr3 + 50569561 50569561 50569561 GGCAGCTTCTCCGGCTGGTGGGTGGGTGGGGCAGCCTTTCAGGCAGGTATGCATGGGAGGTGGGG GGCAGCTTCTCCGGCTGGTGGGTGGGTGGGGCGGCCTTTCAGGCAGGTATGCATGGGAGGTGGGG A G HEMK1 Ensembl:ENSG00000114735 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:50569547..50569694 26863196 MeRIP-seq:(Medium) rs996899823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757267,Human_RBP_ID_9434625 Human_Splice_Rec_434491,Human_Splice_Rec_434511 87420 RMVar_ID_87420 Human_SNP_ID_132825745 m1A Human chr3 + 50611683 50611683 50611683 GTCCCCGCGGCAGCGGCGACTCCGGAGTGGGGACTCGGCTGGACGGCGGCGGCTGGAGGGAACCA GTCCCCGCGGCAGCGGCGACTCCGGAGTGGGGGCTCGGCTGGACGGCGGCGGCTGGAGGGAACCA A G MAPKAPK3 Ensembl:ENSG00000114738 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50611602..50611716 26863196 MeRIP-seq:(Medium) rs1461345580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_434589 87421 RMVar_ID_87421 Human_SNP_ID_132827080 m1A Human chr3 - 50617129 50617129 50617129 GGGCCGAGAGTCGCGCTGCCGGCGCCCACGTGACCTCCCCCCCCTCCCCACCCCCCCCTCCCCCA GGGCCGAGAGTCGCGCTGCCGGCGCCCACGTGCCCTCCCCCCCCTCCCCACCCCCCCCTCCCCCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:50617076..50617150 26863196 MeRIP-seq:(Medium) rs1296766431 Functional Loss SNV dbSNP153 33..33 33 - - - 87422 RMVar_ID_87422 Human_SNP_ID_132827110 m1A Human chr3 + 50617225 50617225 50617225 CGCCTCTCCTGCCCCTCGCCGGTACCTCAGCAAGGTGCGTTGCCGCCAGGTACGCCCTCGCTGGG CGCCTCTCCTGCCCCTCGCCGGTACCTCAGCAGGGTGCGTTGCCGCCAGGTACGCCCTCGCTGGG A G MAPKAPK3 Ensembl:ENSG00000114738 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:50617151..50617250 26863410 MeRIP-seq:(Medium) rs567781237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757271,Human_RBP_ID_5474421 Human_Splice_Rec_434623,Human_Splice_Rec_434641,Human_Splice_Rec_434661 RMVar_hsa_circ_83905,RMVar_hsa_circ_218446 87423 RMVar_ID_87423 Human_SNP_ID_132834180 m1A Human chr3 - 50648051 50648051 50648051 CAGGCTGAGAGGCCAGGCTCCTCCAAGGCCCCATGAGCTACTGGTTGTTGCAGCCCTGTGAGGCA CAGGCTGAGAGGCCAGGCTCCTCCAAGGCCCCGTGAGCTACTGGTTGTTGCAGCCCTGTGAGGCA T C HSALNG0026054 RNACentral:URS0000EA0141 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50648006..50648156 32194978 MeRIP-seq:(Medium) rs747943698 Functional Loss SNV dbSNP153 33..33 33 - - - 87424 RMVar_ID_87424 Human_SNP_ID_132840295 m1A Human chr3 + 50675270 50675270 50675270 CCCGCGGGGCCGCGCCCGGCACGGCCATGTGGACCCCCACGGAGGAGGAGAAATACGGCGTAGGT CCCGCGGGGCCGCGCCCGGCACGGCCATGTGGGCCCCCACGGAGGAGGAGAAATACGGCGTAGGT A G DOCK3 Ensembl:ENSG00000088538 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50675165..50675275 26863196 MeRIP-seq:(Medium) rs769279606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4748067,Human_RBP_ID_18446775 Human_Splice_Rec_434689 87425 RMVar_ID_87425 Human_SNP_ID_133007929 m1A Human chr3 - 51385355 51385337 51385355 AGCCAGCGCCACCGCCAGCCCCTGCGTGGCCCACATCCTCCTCATCCTCCTCATCCTCCTCCTCC AGCCAGCGCCACCGCCAGCCCCTGCGTGGCCC__________________TCATCCTCCTCCTCC AGGAGGATGAGGAGGATGT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:51385306..51385480 26863196 MeRIP-seq:(Medium) rs1163365289 Functional Loss DEL dbSNP153 33..50 33 - - - 87426 RMVar_ID_87426 Human_SNP_ID_133007953 m1A Human chr3 - 51385355 51385355 51385355 AGCCAGCGCCACCGCCAGCCCCTGCGTGGCCCACATCCTCCTCATCCTCCTCATCCTCCTCCTCC AGCCAGCGCCACCGCCAGCCCCTGCGTGGCCCTCATCCTCCTCATCCTCCTCATCCTCCTCCTCC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:51385306..51385480 26863196 MeRIP-seq:(Medium) rs1553620690 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 87427 RMVar_ID_87427 Human_SNP_ID_133007975 m1A Human chr3 + 51385406 51385398 51385406 CGGTGGCGCTGGCTCTGAGCGTGCTGCCGGGCAGCCGGGCGCTGCGGCCGGGCGACTGCGAAGGT CGGTGGCGCTGGCTCTGAGCGTGCT________GCCGGGCGCTGCGGCCGGGCGACTGCGAAGGT TGCCGGGCA T MANF Ensembl:ENSG00000145050 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:51385301..51385481 26863410 MeRIP-seq:(Medium) rs1553620707 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_248342,Human_RBP_ID_4748093,Human_RBP_ID_5149947,Human_RBP_ID_5325265,Human_RBP_ID_5530485,Human_RBP_ID_8943488,Human_RBP_ID_9348852,Human_RBP_ID_9434626,Human_RBP_ID_17660709,Human_RBP_ID_18194855,Human_RBP_ID_18424226,Human_RBP_ID_19117659,Human_RBP_ID_20971213,Human_RBP_ID_22455915,Human_RBP_ID_23026359,Human_RBP_ID_24553963,Human_RBP_ID_26346297 Human_Splice_Rec_434793,Human_Splice_Rec_434799 87428 RMVar_ID_87428 Human_SNP_ID_133008220 m1A Human chr3 - 51386159 51386159 51386159 CGGGAGATGCTCAGCAATCACCAAGCTGTTCCAATCCACCAGAAAAGAACTCCGCCAGCAATTTT CGGGAGATGCTCAGCAATCACCAAGCTGTTCCGATCCACCAGAAAAGAACTCCGCCAGCAATTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51386156..51386383 26863196 MeRIP-seq:(Medium) rs1478332038 Functional Loss SNV dbSNP153 33..33 33 - - - 87429 RMVar_ID_87429 Human_SNP_ID_133008228 m1A Human chr3 + 51386174 51386174 51386174 GTTCTTTTCTGGTGGATTGGAACAGCTTGGTGATTGCTGAGCATCTCCCGTCCCTCTCTTTTCCA GTTCTTTTCTGGTGGATTGGAACAGCTTGGTGTTTGCTGAGCATCTCCCGTCCCTCTCTTTTCCA A T MANF Ensembl:ENSG00000145050 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51386171..51386350 26863196 MeRIP-seq:(Medium) rs528848502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1629161,Human_RBP_ID_8575575,Human_RBP_ID_22551615,Human_RBP_ID_22676483,Human_RBP_ID_24009729 87430 RMVar_ID_87430 Human_SNP_ID_133008282 m1A Human chr3 + 51386286 51386286 51386286 AGATGTCACATTCTCACCAGCCACTATTGAAAACGAACTTATAAAGTTCTGCCGGGAAGCAAGAG AGATGTCACATTCTCACCAGCCACTATTGAAACCGAACTTATAAAGTTCTGCCGGGAAGCAAGAG A C MANF Ensembl:ENSG00000145050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:51386201..51386300;chr3:51386201..51386325 32194978 MeRIP-seq:(Medium) rs781878256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604870,Human_RBP_ID_1965194,Human_RBP_ID_4748098,Human_RBP_ID_8575576,Human_RBP_ID_9333755,Human_RBP_ID_9393707,Human_RBP_ID_17661448,Human_RBP_ID_27823297 Human_Splice_Rec_434794,Human_Splice_Rec_434795,Human_Splice_Rec_434800,Human_Splice_Rec_434801,Human_Splice_Rec_434807 RMVar_hsa_circ_31675 87431 RMVar_ID_87431 Human_SNP_ID_133008283 m1A Human chr3 + 51386286 51386286 51386286 AGATGTCACATTCTCACCAGCCACTATTGAAAACGAACTTATAAAGTTCTGCCGGGAAGCAAGAG AGATGTCACATTCTCACCAGCCACTATTGAAAGCGAACTTATAAAGTTCTGCCGGGAAGCAAGAG A G MANF Ensembl:ENSG00000145050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:51386201..51386300;chr3:51386201..51386325 32194978 MeRIP-seq:(Medium) rs781878256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604870,Human_RBP_ID_1965194,Human_RBP_ID_4748098,Human_RBP_ID_8575576,Human_RBP_ID_9333755,Human_RBP_ID_9393707,Human_RBP_ID_17661448,Human_RBP_ID_27823297 Human_Splice_Rec_434794,Human_Splice_Rec_434795,Human_Splice_Rec_434800,Human_Splice_Rec_434801,Human_Splice_Rec_434807 RMVar_hsa_circ_31675 87432 RMVar_ID_87432 Human_SNP_ID_133009025 m1A Human chr3 + 51389048 51389048 51389048 ACTACATCCGGAAGATAAATGAACTGATGCCTAAATATGCCCCCAAGGCAGCCAGTGCACGGACC ACTACATCCGGAAGATAAATGAACTGATGCCTGAATATGCCCCCAAGGCAGCCAGTGCACGGACC A G MANF Ensembl:ENSG00000145050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51387781..51389201 32194978 MeRIP-seq:(Medium) rs782155721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604876,Human_RBP_ID_1313481,Human_RBP_ID_1629170,Human_RBP_ID_7207710,Human_RBP_ID_14881177,Human_RBP_ID_17661452,Human_RBP_ID_22455467,Human_RBP_ID_22768907,Human_RBP_ID_24498485,Human_RBP_ID_27320486 Human_miRNA_ID_337584,Human_miRNA_ID_795046 87433 RMVar_ID_87433 Human_SNP_ID_133010046 m1A Human chr3 + 51392083 51392083 51392083 TACCTGCGTGGCGGCGGCGGGAGCAGTCGGCGAAGTAGCAGCAGCAGCGCCGCCGCTTCCACGCC TACCTGCGTGGCGGCGGCGGGAGCAGTCGGCGTAGTAGCAGCAGCAGCGCCGCCGCTTCCACGCC A T RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:51391938..51392150 26863196 MeRIP-seq:(Medium) rs1327539313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18007870,Human_RBP_ID_27503509 87434 RMVar_ID_87434 Human_SNP_ID_133010058 m1A Human chr3 - 51392116 51392116 51392116 AGCGGGTCGGCGGGCGCGGGCGGCCCTGGGGGAGGCGTGGAAGCGGCGGCGCTGCTGCTGCTACT AGCGGGTCGGCGGGCGCGGGCGGCCCTGGGGGGGGCGTGGAAGCGGCGGCGCTGCTGCTGCTACT T C lnc-DCAF1-1 RNACentral:URS0000D5C289 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51392066..51392266 32194978 MeRIP-seq:(Medium) rs1553621657 Functional Loss SNV dbSNP153 33..33 33 - - - 87435 RMVar_ID_87435 Human_SNP_ID_133010202 m1A Human chr3 + 51392359 51392359 51392359 TACGACGACCGTGGGCGCCCCTATGGCTACCCAGCTGTGTGTGAGGAGGACCTGATGCCCGAGGA TACGACGACCGTGGGCGCCCCTATGGCTACCCCGCTGTGTGTGAGGAGGACCTGATGCCCGAGGA A C RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51392116..51392366 32194978 MeRIP-seq:(Medium) rs782171550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4748159,Human_RBP_ID_7207721,Human_RBP_ID_8875046,Human_RBP_ID_14881199,Human_RBP_ID_27320512 87436 RMVar_ID_87436 Human_SNP_ID_133010203 m1A Human chr3 + 51392359 51392359 51392359 TACGACGACCGTGGGCGCCCCTATGGCTACCCAGCTGTGTGTGAGGAGGACCTGATGCCCGAGGA TACGACGACCGTGGGCGCCCCTATGGCTACCCGGCTGTGTGTGAGGAGGACCTGATGCCCGAGGA A G RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51392116..51392366 32194978 MeRIP-seq:(Medium) rs782171550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4748159,Human_RBP_ID_7207721,Human_RBP_ID_8875046,Human_RBP_ID_14881199,Human_RBP_ID_27320512 87437 RMVar_ID_87437 Human_SNP_ID_133010522 m1A Human chr3 + 51393251 51393251 51393251 CCCATTCACCATATGAGGAACGGAGTAGGACCAAGGGCAGTGGGCAGCAGTCAGAGCGGGGCTCC CCCATTCACCATATGAGGAACGGAGTAGGACCGAGGGCAGTGGGCAGCAGTCAGAGCGGGGCTCC A G RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51393200..51393368 26863196 MeRIP-seq:(Medium) rs1553621925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248712,Human_RBP_ID_784937,Human_RBP_ID_7207734,Human_RBP_ID_8873247,Human_RBP_ID_9302926,Human_RBP_ID_14881237,Human_RBP_ID_18811249 Human_miRNA_ID_246477,Human_miRNA_ID_248994 87438 RMVar_ID_87438 Human_SNP_ID_133010553 m1A Human chr3 + 51393315 51393315 51393315 CGACCGCACCCCTGAGCGCAGCCGCAAGGAGAACCACTCCAGTGAAGGGACCAAGGAGTCCAGCA CGACCGCACCCCTGAGCGCAGCCGCAAGGAGAGCCACTCCAGTGAAGGGACCAAGGAGTCCAGCA A G RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51393264..51393365 32194978 MeRIP-seq:(Medium) rs1553621941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1629184,Human_RBP_ID_3711375,Human_RBP_ID_8873248,Human_RBP_ID_14881239 87439 RMVar_ID_87439 Human_SNP_ID_133010623 m1A Human chr3 + 51393467 51393467 51393467 AGAAGGCAAGAGACAGCGAGCGCAATCACCGGACCACAGAGGCCGAGCCCAAGCCTCTGGAAGAG AGAAGGCAAGAGACAGCGAGCGCAATCACCGGGCCACAGAGGCCGAGCCCAAGCCTCTGGAAGAG A G RBM15B Ensembl:ENSG00000259956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51393093..51393508 26863196 MeRIP-seq:(Medium) rs782712843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7207740,Human_RBP_ID_8873251,Human_RBP_ID_9302927,Human_RBP_ID_17290548,Human_RBP_ID_27320531 87440 RMVar_ID_87440 Human_SNP_ID_133010875 m1A Human chr3 + 51394113 51394113 51394113 TGTCTTTCCCAGCGTCATGTTTGTGTCACAAAAGCAGTTATTTTAAAATCTGATCCCCTCTCTAC TGTCTTTCCCAGCGTCATGTTTGTGTCACAAAGGCAGTTATTTTAAAATCTGATCCCCTCTCTAC A G RBM15B Ensembl:ENSG00000259956 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51394063..51394164 32194978 MeRIP-seq:(Medium) rs782316284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7207761,Human_RBP_ID_8575599 87441 RMVar_ID_87441 Human_SNP_ID_133017657 m1A Human chr3 - 51420357 51420357 51420357 AAAGGGCTTGGAGAAACAGCAACCGTGCTGACAAAAGAGGCTGACCTGCCCATGACTGCTGCCTC AAAGGGCTTGGAGAAACAGCAACCGTGCTGACGAAAGAGGCTGACCTGCCCATGACTGCTGCCTC T C DCAF1 Ensembl:ENSG00000145041 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51420309..51420460 32194978 MeRIP-seq:(Medium) rs782723139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604929,Human_RBP_ID_14881611 RMVar_hsa_circ_2920,RMVar_hsa_circ_218498,RMVar_hsa_circ_59445,RMVar_hsa_circ_108208,RMVar_hsa_circ_50678,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_308353,RMVar_hsa_circ_265593,RMVar_hsa_circ_12936 87442 RMVar_ID_87442 Human_SNP_ID_133021195 m1A Human chr3 + 51435168 51435168 51435168 ACTCTACCACACTTCCACCCACTCCTTCTCCCAAGATGCAGCTAAACTGTGTGACACCCATTATA ACTCTACCACACTTCCACCCACTCCTTCTCCCTAGATGCAGCTAAACTGTGTGACACCCATTATA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51435142..51435215 26863196 MeRIP-seq:(Medium) rs1168844480 Functional Loss SNV dbSNP153 33..33 33 - - - 87443 RMVar_ID_87443 Human_SNP_ID_133034004 m1A Human chr3 - 51483825 51483825 51483825 TTTTTATTTTTGCTTCCTTAGGCAAAGCCATGACTACAGTAGTGGTACATGTGGACTCCAAAGCT TTTTTATTTTTGCTTCCTTAGGCAAAGCCATGGCTACAGTAGTGGTACATGTGGACTCCAAAGCT T C DCAF1 Ensembl:ENSG00000145041 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51483774..51483877 26863196 MeRIP-seq:(Medium) rs781971559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933796,Human_RBP_ID_1033744,Human_RBP_ID_3964094,Human_RBP_ID_5149949,Human_RBP_ID_5530926,Human_RBP_ID_7207970,Human_RBP_ID_9348537,Human_RBP_ID_14882146,Human_RBP_ID_18423992,Human_RBP_ID_19010516,Human_RBP_ID_22677941,Human_RBP_ID_24009850,Human_RBP_ID_25762796,Human_RBP_ID_27823301 Human_Splice_Rec_434818,Human_Splice_Rec_434864 RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_34996,RMVar_hsa_circ_310475,RMVar_hsa_circ_13970,RMVar_hsa_circ_218511,RMVar_hsa_circ_218512,RMVar_hsa_circ_45759,RMVar_hsa_circ_218519,RMVar_hsa_circ_14826,RMVar_hsa_circ_271332,RMVar_hsa_circ_39356,RMVar_hsa_circ_218515,RMVar_hsa_circ_300256,RMVar_hsa_circ_218516,RMVar_hsa_circ_361291,RMVar_hsa_circ_305308,RMVar_hsa_circ_295589,RMVar_hsa_circ_218517,RMVar_hsa_circ_218518,RMVar_hsa_circ_321888,RMVar_hsa_circ_339496,RMVar_hsa_circ_353200,RMVar_hsa_circ_218520 87444 RMVar_ID_87444 Human_SNP_ID_133038749 m1A Human chr3 + 51499906 51499904 51499906 GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCCGACCCCGCCAGTGGCCACAGTTCACACACACACA GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCC__CCCCGCCAGTGGCCACAGTTCACACACACACA CGA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:51499795..51499908 26863196 MeRIP-seq:(Medium) rs1553663456 Functional Loss DEL dbSNP153 32..33 33 - - - 87445 RMVar_ID_87445 Human_SNP_ID_133038753 m1A Human chr3 + 51499906 51499906 51499906 GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCCGACCCCGCCAGTGGCCACAGTTCACACACACACA GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCCGCCCCCGCCAGTGGCCACAGTTCACACACACACA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:51499795..51499908 26863196 MeRIP-seq:(Medium) rs782631822 Functional Loss SNV dbSNP153 33..33 33 - - - 87446 RMVar_ID_87446 Human_SNP_ID_133038754 m1A Human chr3 + 51499906 51499906 51499906 GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCCGACCCCGCCAGTGGCCACAGTTCACACACACACA GTCCGAGGCGGCTCCGCCGCTGCCCCCCCCCGGCCCCGCCAGTGGCCACAGTTCACACACACACA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:51499795..51499908 26863196 MeRIP-seq:(Medium) rs782631822 Functional Loss SNV dbSNP153 33..33 33 - - - 87447 RMVar_ID_87447 Human_SNP_ID_133048495 m1A Human chr3 + 51538805 51538805 51538805 GCGCCCGGGCCTGGCCGGCTGCTTCCCGCCTCAGCCGCCGCCCCCGCCTCCGCCGCCGCAGACTT GCGCCCGGGCCTGGCCGGCTGCTTCCCGCCTCCGCCGCCGCCCCCGCCTCCGCCGCCGCAGACTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:51538755..51538852 26863196 MeRIP-seq:(Medium) rs911445897 Functional Loss SNV dbSNP153 33..33 33 - - - 87448 RMVar_ID_87448 Human_SNP_ID_133048496 m1A Human chr3 + 51538805 51538805 51538805 GCGCCCGGGCCTGGCCGGCTGCTTCCCGCCTCAGCCGCCGCCCCCGCCTCCGCCGCCGCAGACTT GCGCCCGGGCCTGGCCGGCTGCTTCCCGCCTCGGCCGCCGCCCCCGCCTCCGCCGCCGCAGACTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:51538755..51538852 26863196 MeRIP-seq:(Medium) rs911445897 Functional Loss SNV dbSNP153 33..33 33 - - - 87449 RMVar_ID_87449 Human_SNP_ID_133060738 m1A Human chr3 - 51590458 51590458 51590458 CTTCCGCATCCTCCAGCTCCACGTCCGGGTCCAGGTCTGGATCGCTCCCTGAGGCAGATTCGTCT CTTCCGCATCCTCCAGCTCCACGTCCGGGTCCGGGTCTGGATCGCTCCCTGAGGCAGATTCGTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51590409..51590535 26863196 MeRIP-seq:(Medium) rs749894683 Functional Loss SNV dbSNP153 33..33 33 - - - 87450 RMVar_ID_87450 Human_SNP_ID_133078380 m1A Human chr3 - 51663917 51663917 51663917 ACAAACACACATACCTGGTCAGCTTCCTTCCCACCCCCTAAAAAGACCCCACTTCACATGGGATC ACAAACACACATACCTGGTCAGCTTCCTTCCCCCCCCCTAAAAAGACCCCACTTCACATGGGATC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51663869..51663958 26863196 MeRIP-seq:(Medium) rs1160313963 Functional Loss SNV dbSNP153 33..33 33 - - - 87451 RMVar_ID_87451 Human_SNP_ID_133078381 m1A Human chr3 + 51663922 51663922 51663922 CATGTGAAGTGGGGTCTTTTTAGGGGGTGGGAAGGAAGCTGACCAGGTATGTGTGTTTGTGAGTG CATGTGAAGTGGGGTCTTTTTAGGGGGTGGGAGGGAAGCTGACCAGGTATGTGTGTTTGTGAGTG A G RAD54L2,TEX264 Ensembl:ENSG00000164080,Ensembl:ENSG00000164081 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51663885..51663957 26863196 MeRIP-seq:(Medium) rs1474499887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604953,Human_RBP_ID_7208240,Human_RBP_ID_17194915,Human_RBP_ID_24010032 87452 RMVar_ID_87452 Human_SNP_ID_133080132 m1A Human chr3 + 51671686 51671686 51671686 CGTGGGGCTCCGTGAGGAGGTGGGCGAAGAGAAAGGCTCTGAGTAAATAGGCAAGGCCCGGGGTG CGTGGGGCTCCGTGAGGAGGTGGGCGAAGAGAGAGGCTCTGAGTAAATAGGCAAGGCCCGGGGTG A G TEX264 Ensembl:ENSG00000164081 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51671681..51671774 26863196 MeRIP-seq:(Medium) rs1335801775 Functional Loss SNV dbSNP153 33..33 33 - - - 87453 RMVar_ID_87453 Human_SNP_ID_133082400 m1A Human chr3 + 51681495 51681495 51681495 TTGGTGGAGAGCAACAGAAGGCTTTGAAGGGGAAAGTTGAGCTGAGTCTTGCAGGATGGGCAGGA TTGGTGGAGAGCAACAGAAGGCTTTGAAGGGGTAAGTTGAGCTGAGTCTTGCAGGATGGGCAGGA A T TEX264 Ensembl:ENSG00000164081 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51681492..51681696 26863196 MeRIP-seq:(Medium) rs1345392560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78692,RMVar_hsa_circ_218544,RMVar_hsa_circ_121003,RMVar_hsa_circ_126568,RMVar_hsa_circ_289538,RMVar_hsa_circ_218545,RMVar_hsa_circ_218546,RMVar_hsa_circ_218547 87454 RMVar_ID_87454 Human_SNP_ID_133087713 m1A Human chr3 + 51704240 51704240 51704240 GACTATTTTCTGCACCAGCCCCCAGGGCTGCCACCCCTGTTGTGTCTTTTTTTCAGACTCACAGT GACTATTTTCTGCACCAGCCCCCAGGGCTGCCCCCCCTGTTGTGTCTTTTTTTCAGACTCACAGT A C TEX264 Ensembl:ENSG00000164081 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937183,Human_RBP_ID_17661141,Human_RBP_ID_24010229 Human_miRNA_ID_1379153 GWAS_ID_10683,GWAS_ID_10684,GWAS_ID_10685,GWAS_ID_10686,GWAS_ID_10687,GWAS_ID_10688,GWAS_ID_10689,GWAS_ID_10690,GWAS_ID_10691,GWAS_ID_10692,GWAS_ID_10693,GWAS_ID_10694,GWAS_ID_10695,GWAS_ID_10696,GWAS_ID_10697,GWAS_ID_10698,GWAS_ID_10699,GWAS_ID_10700,GWAS_ID_10701,GWAS_ID_10702,GWAS_ID_10703,GWAS_ID_10704,GWAS_ID_10705,GWAS_ID_10706,GWAS_ID_10707,GWAS_ID_10708,GWAS_ID_10709,GWAS_ID_10710,GWAS_ID_10711,GWAS_ID_10712,GWAS_ID_10713,GWAS_ID_10714 RMVar_hsa_circ_218544,RMVar_hsa_circ_121003,RMVar_hsa_circ_126568,RMVar_hsa_circ_218545,RMVar_hsa_circ_76938,RMVar_hsa_circ_218549 87455 RMVar_ID_87455 Human_SNP_ID_133087714 m1A Human chr3 + 51704240 51704240 51704240 GACTATTTTCTGCACCAGCCCCCAGGGCTGCCACCCCTGTTGTGTCTTTTTTTCAGACTCACAGT GACTATTTTCTGCACCAGCCCCCAGGGCTGCCGCCCCTGTTGTGTCTTTTTTTCAGACTCACAGT A G TEX264 Ensembl:ENSG00000164081 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937183,Human_RBP_ID_17661141,Human_RBP_ID_24010229 Human_miRNA_ID_1379153 GWAS_ID_10683,GWAS_ID_10684,GWAS_ID_10685,GWAS_ID_10686,GWAS_ID_10687,GWAS_ID_10688,GWAS_ID_10689,GWAS_ID_10690,GWAS_ID_10691,GWAS_ID_10692,GWAS_ID_10693,GWAS_ID_10694,GWAS_ID_10695,GWAS_ID_10696,GWAS_ID_10697,GWAS_ID_10698,GWAS_ID_10699,GWAS_ID_10700,GWAS_ID_10701,GWAS_ID_10702,GWAS_ID_10703,GWAS_ID_10704,GWAS_ID_10705,GWAS_ID_10706,GWAS_ID_10707,GWAS_ID_10708,GWAS_ID_10709,GWAS_ID_10710,GWAS_ID_10711,GWAS_ID_10712,GWAS_ID_10713,GWAS_ID_10714 RMVar_hsa_circ_218544,RMVar_hsa_circ_121003,RMVar_hsa_circ_126568,RMVar_hsa_circ_218545,RMVar_hsa_circ_76938,RMVar_hsa_circ_218549 87456 RMVar_ID_87456 Human_SNP_ID_133087715 m1A Human chr3 + 51704240 51704240 51704240 GACTATTTTCTGCACCAGCCCCCAGGGCTGCCACCCCTGTTGTGTCTTTTTTTCAGACTCACAGT GACTATTTTCTGCACCAGCCCCCAGGGCTGCCTCCCCTGTTGTGTCTTTTTTTCAGACTCACAGT A T TEX264 Ensembl:ENSG00000164081 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937183,Human_RBP_ID_17661141,Human_RBP_ID_24010229 Human_miRNA_ID_1379153 GWAS_ID_10683,GWAS_ID_10684,GWAS_ID_10685,GWAS_ID_10686,GWAS_ID_10687,GWAS_ID_10688,GWAS_ID_10689,GWAS_ID_10690,GWAS_ID_10691,GWAS_ID_10692,GWAS_ID_10693,GWAS_ID_10694,GWAS_ID_10695,GWAS_ID_10696,GWAS_ID_10697,GWAS_ID_10698,GWAS_ID_10699,GWAS_ID_10700,GWAS_ID_10701,GWAS_ID_10702,GWAS_ID_10703,GWAS_ID_10704,GWAS_ID_10705,GWAS_ID_10706,GWAS_ID_10707,GWAS_ID_10708,GWAS_ID_10709,GWAS_ID_10710,GWAS_ID_10711,GWAS_ID_10712,GWAS_ID_10713,GWAS_ID_10714 RMVar_hsa_circ_218544,RMVar_hsa_circ_121003,RMVar_hsa_circ_126568,RMVar_hsa_circ_218545,RMVar_hsa_circ_76938,RMVar_hsa_circ_218549 87457 RMVar_ID_87457 Human_SNP_ID_133141198 m1A Human chr3 + 51935493 51935493 51935493 GTCCTGGTGTCCGAAGCTAGAGGGCCGGGCAGAGCAGGATAGTGGGGATAGGGGTACTGCATGAA GTCCTGGTGTCCGAAGCTAGAGGGCCGGGCAGGGCAGGATAGTGGGGATAGGGGTACTGCATGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51935492..51935576 26863196 MeRIP-seq:(Medium) rs1424472589 Functional Loss SNV dbSNP153 33..33 33 - - - 87458 RMVar_ID_87458 Human_SNP_ID_133141470 m1A Human chr3 - 51936306 51936306 51936306 CCGCAGCAAGCTCATTCTCATTTGGGAGGCCCAGAGCTGCCAGCACTTGTACACCTTCACAGGAC CCGCAGCAAGCTCATTCTCATTTGGGAGGCCCGGAGCTGCCAGCACTTGTACACCTTCACAGGAC T C RRP9 Ensembl:ENSG00000114767 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51936251..51936350 32194978 MeRIP-seq:(Medium) rs1421964190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4748655 Human_Splice_Rec_435404,Human_Splice_Rec_435405 Human_miRNA_ID_2314730,Human_miRNA_ID_2317890,Human_miRNA_ID_2321047,Human_miRNA_ID_2324202,Human_miRNA_ID_2423438,Human_miRNA_ID_2433098,Human_miRNA_ID_2518584,Human_miRNA_ID_2521754,Human_miRNA_ID_2773603,Human_miRNA_ID_2820949,Human_miRNA_ID_2827084,Human_miRNA_ID_2830233,Human_miRNA_ID_2834351,Human_miRNA_ID_2839719 RMVar_hsa_circ_218550,RMVar_hsa_circ_81058,RMVar_hsa_circ_86850,RMVar_hsa_circ_112552,RMVar_hsa_circ_104490,RMVar_hsa_circ_83171,RMVar_hsa_circ_218554,RMVar_hsa_circ_80303,RMVar_hsa_circ_218555,RMVar_hsa_circ_218552,RMVar_hsa_circ_218553,RMVar_hsa_circ_218551,RMVar_hsa_circ_82206,RMVar_hsa_circ_93475,RMVar_hsa_circ_218562,RMVar_hsa_circ_218563 87459 RMVar_ID_87459 Human_SNP_ID_133143503 m1A Human chr3 + 51943399 51943399 51943399 GCCGAAGCCCTGGGTACAGACTGAGGGCCCTGAGAAGAAGAAGGGCCGGCAGGCAGGAAGGGAGG GCCGAAGCCCTGGGTACAGACTGAGGGCCCTGTGAAGAAGAAGGGCCGGCAGGCAGGAAGGGAGG A T PARP3 Ensembl:ENSG00000041880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51943257..51943488 26863196 MeRIP-seq:(Medium) rs778869919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_435422,Human_Splice_Rec_435442,Human_Splice_Rec_435462,Human_Splice_Rec_435482,Human_Splice_Rec_435502 87460 RMVar_ID_87460 Human_SNP_ID_133147547 m1A Human chr3 + 51957592 51957592 51957592 CTGGCAGTGCCCCCTCTTTGGGGTGCCCCCTGACAAGCCCAGCCAGTTCATTCCAGTCAAAAGGG CTGGCAGTGCCCCCTCTTTGGGGTGCCCCCTGGCAAGCCCAGCCAGTTCATTCCAGTCAAAAGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51957543..51957693 26863196 MeRIP-seq:(Medium) rs1201338096 Functional Loss SNV dbSNP153 33..33 33 - - - 87461 RMVar_ID_87461 Human_SNP_ID_133147560 m1A Human chr3 + 51957644 51957643 51957644 CCAGTCAAAAGGGTATCAGTGGAAGCAGCAAGAAATCTGCAGGTGGTGGGGAGAGAAGCCTGGCC CCAGTCAAAAGGGTATCAGTGGAAGCAGCAAG_AATCTGCAGGTGGTGGGGAGAGAAGCCTGGCC GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51957553..51957803 32194978 MeRIP-seq:(Medium) rs1403955533 Functional Loss DEL dbSNP153 33..33 33 - - - 87462 RMVar_ID_87462 Human_SNP_ID_133147783 m1A Human chr3 + 51958349 51958349 51958349 GTCCCCCCAGAGGTAGACTTGGCCGTCTCTAGACTGGAGAGAGGGATATAGAGGGGAGACAAAGG GTCCCCCCAGAGGTAGACTTGGCCGTCTCTAGGCTGGAGAGAGGGATATAGAGGGGAGACAAAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51958300..51959077 32194978 MeRIP-seq:(Medium) rs201708744 Functional Loss SNV dbSNP153 33..33 33 - - - 87463 RMVar_ID_87463 Human_SNP_ID_133148734 m1A Human chr3 - 51961212 51961212 51961212 CAGAATGAGCGGCTCGGACGGGGGACTGGAGGAGGAGCCAGAGCTCAGCATCACCCTCACGCTGC CAGAATGAGCGGCTCGGACGGGGGACTGGAGGTGGAGCCAGAGCTCAGCATCACCCTCACGCTGC T A PCBP4,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000272762 Protein coding,lincRNA CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51961161..51961330 26863196 MeRIP-seq:(Medium) rs1274083663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758068,Human_RBP_ID_19012475 Human_Splice_Rec_435530,Human_Splice_Rec_435531,Human_Splice_Rec_435554,Human_Splice_Rec_435555,Human_Splice_Rec_435576,Human_Splice_Rec_435577,Human_Splice_Rec_435599,Human_Splice_Rec_435617,Human_Splice_Rec_435640,Human_Splice_Rec_435641,Human_Splice_Rec_435668,Human_Splice_Rec_435669,Human_Splice_Rec_435692,Human_Splice_Rec_435693,Human_Splice_Rec_435710,Human_Splice_Rec_435711,Human_Splice_Rec_435732,Human_Splice_Rec_435733,Human_Splice_Rec_435758,Human_Splice_Rec_435759,Human_Splice_Rec_435776,Human_Splice_Rec_435777,Human_Splice_Rec_435788,Human_Splice_Rec_435789,Human_Splice_Rec_435800,Human_Splice_Rec_435801,Human_Splice_Rec_435812,Human_Splice_Rec_435813,Human_Splice_Rec_435822,Human_Splice_Rec_435823,Human_Splice_Rec_435830,Human_Splice_Rec_435831,Human_Splice_Rec_435840,Human_Splice_Rec_435841,Human_Splice_Rec_435850 RMVar_hsa_circ_24116 87464 RMVar_ID_87464 Human_SNP_ID_133150053 m1A Human chr3 + 51966981 51966981 51966981 TGCGGAGGATGGGAAGGAGTGTGTGCCCAGCCAGGAGCTACAGGGGAGTGGCAAGTGAGGGCAGA TGCGGAGGATGGGAAGGAGTGTGTGCCCAGCCCGGAGCTACAGGGGAGTGGCAAGTGAGGGCAGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51966978..51967057 26863196 MeRIP-seq:(Medium) rs1029671892 Functional Loss SNV dbSNP153 33..33 33 - - - 87465 RMVar_ID_87465 Human_SNP_ID_133150147 m1A Human chr3 + 51967381 51967381 51967381 GCGGCGGCGGCGGCACGGCGGCTGGGCCGCTCAGTCCCACATTGTCCCCGGGAGAGGCGGCCGCT GCGGCGGCGGCGGCACGGCGGCTGGGCCGCTCCGTCCCACATTGTCCCCGGGAGAGGCGGCCGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:51967198..51967462;chr3:51967288..51967414 26863196 MeRIP-seq:(Medium) rs1267524992 Functional Loss SNV dbSNP153 33..33 33 - - - 87466 RMVar_ID_87466 Human_SNP_ID_133150365 m1A Human chr3 - 51967893 51967892 51967893 GCCGGAGCTCGGAGGGACGCGGGCCGGGAGCGAGGCGGAGCCGGGGCTGGCGGGGCCAAGGCGGG GCCGGAGCTCGGAGGGACGCGGGCCGGGAGCG_GGCGGAGCCGGGGCTGGCGGGGCCAAGGCGGG CT C PCBP4,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000272762 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:51967602..51968021 26863196 MeRIP-seq:(Medium) rs1389939750 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26790709 87467 RMVar_ID_87467 Human_SNP_ID_133150621 m1A Human chr3 - 51968757 51968757 51968757 CATGGGCCAGCCCTTGCAGGAGGCCCTTTTGCAAGGCTTAGGGTGTGGCCAGCCCTGAAAGCTAC CATGGGCCAGCCCTTGCAGGAGGCCCTTTTGCGAGGCTTAGGGTGTGGCCAGCCCTGAAAGCTAC T C PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,3'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51968558..51968875 32194978 MeRIP-seq:(Medium) rs994828169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605031,Human_RBP_ID_1104465,Human_RBP_ID_5120313,Human_RBP_ID_8211187,Human_RBP_ID_9434629,Human_RBP_ID_17404641,Human_RBP_ID_18169301 Human_miRNA_ID_2674276,Human_miRNA_ID_2674277,Human_miRNA_ID_2925027,Human_miRNA_ID_2925028 RMVar_hsa_circ_94939,RMVar_hsa_circ_218575,RMVar_hsa_circ_84364,RMVar_hsa_circ_218574 87468 RMVar_ID_87468 Human_SNP_ID_133150754 m1A Human chr3 - 51969326 51969326 51969326 CTCTCCCAGGCTCTGGCTCATGCACATGCAACAGGTGCGTCTGTCTATATGTCTGGGTTCTTGTC CTCTCCCAGGCTCTGGCTCATGCACATGCAACCGGTGCGTCTGTCTATATGTCTGGGTTCTTGTC T G PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,3'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51969276..51969646 32194978 MeRIP-seq:(Medium) rs981546207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605052,Human_RBP_ID_1104099,Human_RBP_ID_2790453,Human_RBP_ID_20920041 RMVar_hsa_circ_94939,RMVar_hsa_circ_218575,RMVar_hsa_circ_84364,RMVar_hsa_circ_218574 87469 RMVar_ID_87469 Human_SNP_ID_133151444 m1A Human chr3 - 51971674 51971672 51971675 AACCACAGGCCCTTCACCAGCACAGCAGCAGCAGGCATGGCAGCAAGCGTGGAGCAGCGCGAGGG AACCACAGGCCCTTCACCAGCACAGCAGCAG___GCATGGCAGCAAGCGTGGAGCAGCGCGAGGG CCTG C PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,5'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51971624..51971732 26863196 MeRIP-seq:(Medium) rs779430059 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1633169,Human_RBP_ID_5605291,Human_RBP_ID_9333762,Human_RBP_ID_18194608,Human_RBP_ID_26824748 Human_Splice_Rec_435846,Human_Splice_Rec_435854,Human_Splice_Rec_435860,Human_Splice_Rec_435878,Human_Splice_Rec_435884,Human_Splice_Rec_435894 RMVar_hsa_circ_218575,RMVar_hsa_circ_84364 87470 RMVar_ID_87470 Human_SNP_ID_133153205 m1A Human chr3 - 51977969 51977968 51977969 TTGGGGTCTCCCCAGAGGCAGGAAGTCTGCTCAGGGGGGCCTGGCAGCCCCACATACAGTAGGAG TTGGGGTCTCCCCAGAGGCAGGAAGTCTGCTC_GGGGGGCCTGGCAGCCCCACATACAGTAGGAG CT C ABHD14B Ensembl:ENSG00000114779 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51977919..51978027 32194978 MeRIP-seq:(Medium) rs776426753 Functional Loss DEL dbSNP153 33..33 33 - - - 87471 RMVar_ID_87471 Human_SNP_ID_133153218 m1A Human chr3 + 51978001 51978001 51978001 TGAGCAGACTTCCTGCCTCTGGGGAGACCCCAATGTCACAGTCCTGGCTGGTCTCACCCCTGGCA TGAGCAGACTTCCTGCCTCTGGGGAGACCCCAGTGTCACAGTCCTGGCTGGTCTCACCCCTGGCA A G ABHD14A-ACY1,ABHD14A Ensembl:ENSG00000114786,Ensembl:ENSG00000248487 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51975154..51980568 32194978 MeRIP-seq:(Medium) rs191551166 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22455922 Human_Splice_Rec_435897,Human_Splice_Rec_435903,Human_Splice_Rec_435909,Human_Splice_Rec_435917,Human_Splice_Rec_435925,Human_Splice_Rec_435929,Human_Splice_Rec_435933,Human_Splice_Rec_435951,Human_Splice_Rec_435971,Human_Splice_Rec_436003,Human_Splice_Rec_436019,Human_Splice_Rec_436057,Human_Splice_Rec_436087,Human_Splice_Rec_436117,Human_Splice_Rec_436145,Human_Splice_Rec_436167,Human_Splice_Rec_436185,Human_Splice_Rec_436207,Human_Splice_Rec_436227,Human_Splice_Rec_436253,Human_Splice_Rec_436275,Human_Splice_Rec_436327,Human_Splice_Rec_436369,Human_Splice_Rec_436393,Human_Splice_Rec_436425,Human_Splice_Rec_436449,Human_Splice_Rec_436473,Human_Splice_Rec_436499,Human_Splice_Rec_436521 RMVar_hsa_circ_77004,RMVar_hsa_circ_82951,RMVar_hsa_circ_218576,RMVar_hsa_circ_293619,RMVar_hsa_circ_218577,RMVar_hsa_circ_218578 87472 RMVar_ID_87472 Human_SNP_ID_133155083 m1A Human chr3 + 51984134 51984134 51984134 TGACGCTCTTCCGCCAGTACCTGCGTATCCGCACTGTCCAGCCCAAGCCTGACTATGGTGAGAAG TGACGCTCTTCCGCCAGTACCTGCGTATCCGCGCTGTCCAGCCCAAGCCTGACTATGGTGAGAAG A G ACY1,ABHD14A-ACY1 Ensembl:ENSG00000243989,Ensembl:ENSG00000114786 Protein coding,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr3:51984017..51984175;chr3:51984085..51984185 26863196,32194978 MeRIP-seq:(Medium) rs1257148621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783162,Human_RBP_ID_4757285,Human_RBP_ID_9393727 Human_Splice_Rec_435936,Human_Splice_Rec_435937,Human_Splice_Rec_435954,Human_Splice_Rec_435955,Human_Splice_Rec_435974,Human_Splice_Rec_435975,Human_Splice_Rec_436006,Human_Splice_Rec_436007,Human_Splice_Rec_436022,Human_Splice_Rec_436023,Human_Splice_Rec_436048,Human_Splice_Rec_436049,Human_Splice_Rec_436090,Human_Splice_Rec_436091,Human_Splice_Rec_436120,Human_Splice_Rec_436121,Human_Splice_Rec_436148,Human_Splice_Rec_436149,Human_Splice_Rec_436170,Human_Splice_Rec_436171,Human_Splice_Rec_436188,Human_Splice_Rec_436189,Human_Splice_Rec_436210,Human_Splice_Rec_436211,Human_Splice_Rec_436230,Human_Splice_Rec_436231,Human_Splice_Rec_436256,Human_Splice_Rec_436257,Human_Splice_Rec_436292,Human_Splice_Rec_436293,Human_Splice_Rec_436308,Human_Splice_Rec_436309,Human_Splice_Rec_436344,Human_Splice_Rec_436348,Human_Splice_Rec_436349,Human_Splice_Rec_436372,Human_Splice_Rec_436373,Human_Splice_Rec_436398,Human_Splice_Rec_436399,Human_Splice_Rec_436428,Human_Splice_Rec_436429,Human_Splice_Rec_436452,Human_Splice_Rec_436453,Human_Splice_Rec_436476,Human_Splice_Rec_436477,Human_Splice_Rec_436524,Human_Splice_Rec_436525,Human_Splice_Rec_436546,Human_Splice_Rec_436548,Human_Splice_Rec_436549,Human_Splice_Rec_436562,Human_Splice_Rec_436563,Human_Splice_Rec_436588,Human_Splice_Rec_436589,Human_Splice_Rec_436612,Human_Splice_Rec_436613,Human_Splice_Rec_436636,Human_Splice_Rec_436637,Human_Splice_Rec_436662,Human_Splice_Rec_436663,Human_Splice_Rec_436684,Human_Splice_Rec_436685,Human_Splice_Rec_436706,Human_Splice_Rec_436707,Human_Splice_Rec_436734,Human_Splice_Rec_436735,Human_Splice_Rec_436750,Human_Splice_Rec_436751,Human_Splice_Rec_436766,Human_Splice_Rec_436767,Human_Splice_Rec_436788,Human_Splice_Rec_436789,Human_Splice_Rec_436814,Human_Splice_Rec_436815,Human_Splice_Rec_436842,Human_Splice_Rec_436843,Human_Splice_Rec_436857,Human_Splice_Rec_436871 RMVar_hsa_circ_81474,RMVar_hsa_circ_82951,RMVar_hsa_circ_218578,RMVar_hsa_circ_104380,RMVar_hsa_circ_218580,RMVar_hsa_circ_218581 87473 RMVar_ID_87473 Human_SNP_ID_133155439 m1A Human chr3 - 51985388 51985388 51985388 GGAGAGTGTAGGGTTGGTGCCTGGCCAGGTCAACACGGTCACCACATAGCCAGGTGCCACCTGGA GGAGAGTGTAGGGTTGGTGCCTGGCCAGGTCAGCACGGTCACCACATAGCCAGGTGCCACCTGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51985376..51985400 32194978 MeRIP-seq:(Medium) rs774953551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7208673 87474 RMVar_ID_87474 Human_SNP_ID_133155854 m1A Human chr3 - 51986645 51986645 51986645 CCAAGCTCATACTTACACCAGGGACTCCGCTCACTATAAAAGACAGTGAAGGCATCAGTGGGATT CCAAGCTCATACTTACACCAGGGACTCCGCTCGCTATAAAAGACAGTGAAGGCATCAGTGGGATT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:51986606..51986706 32194978 MeRIP-seq:(Medium) rs1452178068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14886110,Human_RBP_ID_18008017 87475 RMVar_ID_87475 Human_SNP_ID_133155921 m1A Human chr3 - 51986975 51986975 51986975 AGTGCTGGTAACCCGCACCCCTGGGGAGGTGTAGGGGGAAGGCAGTGTCTTCAGCCTGAGGGGCT AGTGCTGGTAACCCGCACCCCTGGGGAGGTGTGGGGGGAAGGCAGTGTCTTCAGCCTGAGGGGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51986970..51987102 32194978 MeRIP-seq:(Medium) rs934369244 Functional Loss SNV dbSNP153 33..33 33 - - - 87476 RMVar_ID_87476 Human_SNP_ID_133156555 m1A Human chr3 + 51989020 51989020 51989020 TGAGGCTGTGTTCCTCCGTGGGGTGGACATATATACACGCCTGCTGCCTGCCCTTGCCAGTGTGC TGAGGCTGTGTTCCTCCGTGGGGTGGACATATGTACACGCCTGCTGCCTGCCCTTGCCAGTGTGC A G ACY1,ABHD14A-ACY1 Ensembl:ENSG00000243989,Ensembl:ENSG00000114786 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:51988969..51989101 26863196 MeRIP-seq:(Medium) rs560322527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605075,Human_RBP_ID_5120320,Human_RBP_ID_9302354,Human_RBP_ID_17661145 87477 RMVar_ID_87477 Human_SNP_ID_133158166 m1A Human chr3 - 51993866 51993866 51993866 CGTATTGCCAAGGGGCTCAGGCTGTGCCGGCCAAAGGCCAAGGCCAAGGCCAAGGCCAAGGATCA CGTATTGCCAAGGGGCTCAGGCTGTGCCGGCCGAAGGCCAAGGCCAAGGCCAAGGCCAAGGATCA T C RPL29 Ensembl:ENSG00000162244 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs766581795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247519,Human_RBP_ID_9334200,Human_RBP_ID_17404644,Human_RBP_ID_17661150,Human_RBP_ID_18194612,Human_RBP_ID_22455929,Human_RBP_ID_22533911,Human_RBP_ID_23213517,Human_RBP_ID_26823919 Human_miRNA_ID_2217058 RMVar_hsa_circ_94206,RMVar_hsa_circ_103686,RMVar_hsa_circ_94743,RMVar_hsa_circ_218586,RMVar_hsa_circ_218587,RMVar_hsa_circ_218585 87478 RMVar_ID_87478 Human_SNP_ID_133158390 m1A Human chr3 - 51994555 51994555 51994555 CCCTTTACTTTTGCTCTCTGTTCCGTGGAGTGAATCACAAACTCTGAGCCTCAGTTTCCCCATAT CCCTTTACTTTTGCTCTCTGTTCCGTGGAGTGTATCACAAACTCTGAGCCTCAGTTTCCCCATAT T A RPL29 Ensembl:ENSG00000162244 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51994504..51994603 32194978 MeRIP-seq:(Medium) rs1169068860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2790475,Human_RBP_ID_14886328 Human_miRNA_ID_2268630 RMVar_hsa_circ_94206,RMVar_hsa_circ_103686,RMVar_hsa_circ_94743,RMVar_hsa_circ_104771,RMVar_hsa_circ_218586,RMVar_hsa_circ_218587,RMVar_hsa_circ_218585,RMVar_hsa_circ_218588 87479 RMVar_ID_87479 Human_SNP_ID_133158677 m1A Human chr3 + 51995468 51995468 51995468 GTGGTGTGGTTCTTGGACTTGGCCATGTCTGCACCTGGAAGACAAAAGTGGAGATCAGGGTTAAG GTGGTGTGGTTCTTGGACTTGGCCATGTCTGCCCCTGGAAGACAAAAGTGGAGATCAGGGTTAAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51995435..51995795 32194978 MeRIP-seq:(Medium) rs1468035316 Functional Loss SNV dbSNP153 33..33 33 - - - 87480 RMVar_ID_87480 Human_SNP_ID_133173987 m1A Human chr3 + 52054075 52054075 52054075 GTTGGGTAGGTTGGGTGTGACATTGAGGATATACTTGATGCCATACTTGCCGAGCACGTCCAGGT GTTGGGTAGGTTGGGTGTGACATTGAGGATATGCTTGATGCCATACTTGCCGAGCACGTCCAGGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:52054024..52054253 26863196 MeRIP-seq:(Medium) rs1375383352 Functional Loss SNV dbSNP153 33..33 33 - - - 87481 RMVar_ID_87481 Human_SNP_ID_133174759 m1A Human chr3 - 52056463 52056463 52056463 AGGCCGGGGCGGCGGGCGCGCAGCTCGGCGGGAGGCGGGCGCCCGGAGACGCGGCTGGGGCCCGC AGGCCGGGGCGGCGGGCGCGCAGCTCGGCGGGGGGCGGGCGCCCGGAGACGCGGCTGGGGCCCGC T C DUSP7 Ensembl:ENSG00000164086 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:52056366..52056516 26863410 MeRIP-seq:(Medium) rs1025620321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248496,Human_RBP_ID_4758078,Human_RBP_ID_7208841,Human_RBP_ID_9334202 87482 RMVar_ID_87482 Human_SNP_ID_133174761 m1A Human chr3 + 52056471 52056471 52056471 CAGCCGCGTCTCCGGGCGCCCGCCTCCCGCCGAGCTGCGCGCCCGCCGCCCCGGCCTCCCGGCCT CAGCCGCGTCTCCGGGCGCCCGCCTCCCGCCGTGCTGCGCGCCCGCCGCCCCGGCCTCCCGGCCT A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr3:52056377..52056493;chr3:52056396..52056532 26863410 MeRIP-seq:(Medium) rs924523556 Functional Loss SNV dbSNP153 33..33 33 - - - 87483 RMVar_ID_87483 Human_SNP_ID_133174784 m1A Human chr3 - 52056511 52056509 52056511 CGCGCGGAGGGCCGGGCGGGCGGGCGGGACGGAGGCCGGGAGGCCGGGAGGCCGGGGCGGCGGGC CGCGCGGAGGGCCGGGCGGGCGGGCGGGACGG__GCCGGGAGGCCGGGAGGCCGGGGCGGCGGGC CCT C DUSP7 Ensembl:ENSG00000164086 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:52056349..52056550 26863410 MeRIP-seq:(Medium) rs1491484727 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_248496,Human_RBP_ID_4758078 87484 RMVar_ID_87484 Human_SNP_ID_133174786 m1A Human chr3 - 52056511 52056511 52056511 CGCGCGGAGGGCCGGGCGGGCGGGCGGGACGGAGGCCGGGAGGCCGGGAGGCCGGGGCGGCGGGC CGCGCGGAGGGCCGGGCGGGCGGGCGGGACGGCGGCCGGGAGGCCGGGAGGCCGGGGCGGCGGGC T G DUSP7 Ensembl:ENSG00000164086 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:52056349..52056550 26863410 MeRIP-seq:(Medium) rs942185546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248496,Human_RBP_ID_4758078 87485 RMVar_ID_87485 Human_SNP_ID_133181129 m1A Human chr3 + 52083384 52083384 52083384 TGACTGACCTGGCTGCACCTCACACCCCGTGGAGTGACGTACAGTCCCTCATGCCCACTTTCTCC TGACTGACCTGGCTGCACCTCACACCCCGTGGCGTGACGTACAGTCCCTCATGCCCACTTTCTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52083382..52083486 26863196 MeRIP-seq:(Medium) rs1034983009 Functional Loss SNV dbSNP153 33..33 33 - - - 87486 RMVar_ID_87486 Human_SNP_ID_133196994 m1A Human chr3 + 52154595 52154595 52154595 GGTCTCCGTGCCCAGTTCCCCAAGCCCAGACAACCCACAGACAGCGCAGCCAAAAGCCTCTGTCC GGTCTCCGTGCCCAGTTCCCCAAGCCCAGACAGCCCACAGACAGCGCAGCCAAAAGCCTCTGTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52154547..52154655 26863196 MeRIP-seq:(Medium) rs946670317 Functional Loss SNV dbSNP153 33..33 33 - - - 87487 RMVar_ID_87487 Human_SNP_ID_133208246 m1A Human chr3 + 52199240 52199240 52199240 AGTCTTTCCACAGGAGCCAGCATACTTCCTGAACATGGAGAGTGTTGTTCGCCGCTGCCCATTCT AGTCTTTCCACAGGAGCCAGCATACTTCCTGAGCATGGAGAGTGTTGTTCGCCGCTGCCCATTCT A G ALAS1 Ensembl:ENSG00000023330 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52199201..52199325 32194978 MeRIP-seq:(Medium) rs1223280467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605220,Human_RBP_ID_4748929,Human_RBP_ID_24010607 Human_Splice_Rec_437096,Human_Splice_Rec_437118,Human_Splice_Rec_437138,Human_Splice_Rec_437160 RMVar_hsa_circ_34967,RMVar_hsa_circ_86272,RMVar_hsa_circ_64595,RMVar_hsa_circ_64881,RMVar_hsa_circ_218599,RMVar_hsa_circ_63678 87488 RMVar_ID_87488 Human_SNP_ID_133211284 m1A Human chr3 - 52211401 52211401 52211401 CTCTTCAGGATCCGCACAGACTCCAGGGCTCCAGCCAGCAGCATGGGTGGCAGAGAGGTGGTGAA CTCTTCAGGATCCGCACAGACTCCAGGGCTCCTGCCAGCAGCATGGGTGGCAGAGAGGTGGTGAA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52211351..52211400 32194978 MeRIP-seq:(Medium) rs923169759 Functional Loss SNV dbSNP153 33..33 33 - - - 87489 RMVar_ID_87489 Human_SNP_ID_133211285 m1A Human chr3 - 52211401 52211401 52211401 CTCTTCAGGATCCGCACAGACTCCAGGGCTCCAGCCAGCAGCATGGGTGGCAGAGAGGTGGTGAA CTCTTCAGGATCCGCACAGACTCCAGGGCTCCGGCCAGCAGCATGGGTGGCAGAGAGGTGGTGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52211351..52211400 32194978 MeRIP-seq:(Medium) rs923169759 Functional Loss SNV dbSNP153 33..33 33 - - - 87490 RMVar_ID_87490 Human_SNP_ID_133211955 m1A Human chr3 - 52213991 52213991 52213991 TTCTCTGAGGAGAAACAGTTTTTAAATATTAAAGGGAGTAATATACACAAGAGAAATGAAAACAT TTCTCTGAGGAGAAACAGTTTTTAAATATTAACGGGAGTAATATACACAAGAGAAATGAAAACAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52213987..52214069 32194978 MeRIP-seq:(Medium) rs374072823 Functional Loss SNV dbSNP153 33..33 33 - - - 87491 RMVar_ID_87491 Human_SNP_ID_133216025 m1A Human chr3 - 52228729 52228729 52228729 GCCTCCCGGGGAGCTGAGACTAGGGTCCCAGCACAGCCCAGAAACCTTTGGCCACAAGAAGTGGG GCCTCCCGGGGAGCTGAGACTAGGGTCCCAGCGCAGCCCAGAAACCTTTGGCCACAAGAAGTGGG T C AC097637.1,TWF2 Ensembl:ENSG00000173366,Ensembl:ENSG00000247596 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52228679..52228800 26863196 MeRIP-seq:(Medium) rs557883075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605230,Human_RBP_ID_18008117,Human_RBP_ID_26510433 Human_miRNA_ID_625569,Human_miRNA_ID_1359614,Human_miRNA_ID_2552880,Human_miRNA_ID_2552881 RMVar_hsa_circ_93868,RMVar_hsa_circ_218610,RMVar_hsa_circ_85127,RMVar_hsa_circ_101212,RMVar_hsa_circ_218609,RMVar_hsa_circ_218611 87492 RMVar_ID_87492 Human_SNP_ID_133216073 m1A Human chr3 - 52228947 52228947 52228947 CCCTGCCACCATCCTCCTTCCTGGGCTCCAGGAAAGTGTTTCTGGGAGGTCAGGAGGGCTGGCAG CCCTGCCACCATCCTCCTTCCTGGGCTCCAGGGAAGTGTTTCTGGGAGGTCAGGAGGGCTGGCAG T C AC097637.1,TWF2 Ensembl:ENSG00000173366,Ensembl:ENSG00000247596 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52228897..52228966 26863196 MeRIP-seq:(Medium) rs1337122589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605233,Human_RBP_ID_17660715 RMVar_hsa_circ_93868,RMVar_hsa_circ_218610,RMVar_hsa_circ_85127,RMVar_hsa_circ_101212,RMVar_hsa_circ_218609,RMVar_hsa_circ_218611 87493 RMVar_ID_87493 Human_SNP_ID_133216721 m1A Human chr3 - 52230971 52230971 52230971 ACCCACAGGTGAAGACAGAGATCAGTGTGGAAAGCAAGCACCAGACCCTGCAGGGCCTCGCCTTC ACCCACAGGTGAAGACAGAGATCAGTGTGGAAGGCAAGCACCAGACCCTGCAGGGCCTCGCCTTC T C AC097637.1,TWF2 Ensembl:ENSG00000173366,Ensembl:ENSG00000247596 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52230847..52231028 26863196 MeRIP-seq:(Medium) rs748149583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9302355,Human_RBP_ID_22456703 Human_Splice_Rec_437190,Human_Splice_Rec_437210,Human_Splice_Rec_437226,Human_Splice_Rec_437236 RMVar_hsa_circ_40314,RMVar_hsa_circ_218610,RMVar_hsa_circ_85127,RMVar_hsa_circ_101212,RMVar_hsa_circ_218611,RMVar_hsa_circ_218612,RMVar_hsa_circ_104900 87494 RMVar_ID_87494 Human_SNP_ID_133217063 m1A Human chr3 - 52231929 52231929 52231929 TCGCCTGATAACTCCCCCGTGAGTCCTGGGCCAGTGGGAAGTGAGGAGGGGAGCTGGGGCTGAGC TCGCCTGATAACTCCCCCGTGAGTCCTGGGCCGGTGGGAAGTGAGGAGGGGAGCTGGGGCTGAGC T C TWF2 Ensembl:ENSG00000247596 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52231926..52232125 32194978 MeRIP-seq:(Medium) rs1456035407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115697 RMVar_hsa_circ_101212,RMVar_hsa_circ_218611 87495 RMVar_ID_87495 Human_SNP_ID_133219003 m1A Human chr3 - 52239032 52239032 52239032 GGTCAAGCGGAGGGCTCCGACGGCGCGGACGGAGCGAAGCGCCGAGCCATGGCGCACCAAACGGG GGTCAAGCGGAGGGCTCCGACGGCGCGGACGGGGCGAAGCGCCGAGCCATGGCGCACCAAACGGG T C TWF2 Ensembl:ENSG00000247596 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52238999..52239083 26863196 MeRIP-seq:(Medium) rs202101314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784925,Human_RBP_ID_4757293 Human_Splice_Rec_437201,Human_Splice_Rec_437217 87496 RMVar_ID_87496 Human_SNP_ID_133220613 m1A Human chr3 - 52245797 52245765 52245797 GACATGGCGCGGCGGCAGGGGGCTGCCCGCGGAGCGCGGGGCGCTAGGGCTGGGCCGCCCGCGGG GACATGGCGCGGCGGCAGGGGGCTGCCCGCGG________________________________G CCCGCGGGCGGCCCAGCCCTAGCGCCCCGCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52245752..52246005 26863196 MeRIP-seq:(Medium) rs1472521213 Functional Loss DEL dbSNP153 33..64 33 - - - 87497 RMVar_ID_87497 Human_SNP_ID_133220692 m1A Human chr3 + 52245951 52245951 52245951 GACGGCCCCGCTTCCTTCGCGGCTCCAGCTCCAGCCCCGGGGCGGCCGACGCCTCGCGCCGCCCA GACGGCCCCGCTTCCTTCGCGGCTCCAGCTCCGGCCCCGGGGCGGCCGACGCCTCGCGCCGCCCA A G PPM1M Ensembl:ENSG00000164088 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52245829..52245995 26863196 MeRIP-seq:(Medium) rs1344783237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_437241,Human_Splice_Rec_437259,Human_Splice_Rec_437271 RMVar_hsa_circ_85701,RMVar_hsa_circ_218614 87498 RMVar_ID_87498 Human_SNP_ID_133223232 m1A Human chr3 + 52255013 52255013 52255013 TGCCCAGGCCGGAGTGCAATGGCACGATCTCAACTCACCGCAACCTCCGCCTCCTGGGTTCAAGC TGCCCAGGCCGGAGTGCAATGGCACGATCTCATCTCACCGCAACCTCCGCCTCCTGGGTTCAAGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52254738..52255042 26863196 MeRIP-seq:(Medium) rs1435039416 Functional Loss SNV dbSNP153 33..33 33 - - - 87499 RMVar_ID_87499 Human_SNP_ID_133223634 m1A Human chr3 + 52256772 52256772 52256772 CTAAACCTTCCAGCCCTAGGAACTCACCTGCTACCCTCCCGCTACCCTCCCCTTTCCCTCCCTTT CTAAACCTTCCAGCCCTAGGAACTCACCTGCTCCCCTCCCGCTACCCTCCCCTTTCCCTCCCTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52256723..52256925 26863196 MeRIP-seq:(Medium) rs987760464 Functional Loss SNV dbSNP153 33..33 33 - - - 87500 RMVar_ID_87500 Human_SNP_ID_133229041 m1A Human chr3 + 52278392 52278392 52278392 ATGGCGGCGGCTGGGGAAGGCAGCGGCGGCGCAGGGCCGGGGCGGGGCCCGGCGGCGAGCGGGCG ATGGCGGCGGCTGGGGAAGGCAGCGGCGGCGCGGGGCCGGGGCGGGGCCCGGCGGCGAGCGGGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:52278276..52278500 26863410 MeRIP-seq:(Medium) rs747849761 Functional Loss SNV dbSNP153 33..33 33 - - - 87501 RMVar_ID_87501 Human_SNP_ID_133229076 m1A Human chr3 + 52278445 52278445 52278445 GGCGAGCGGGCGGGCTGCCGAGGGGCCAACCCAGGCGGGGCGGGCGCCGCGCCGGCGGCTAGCGG GGCGAGCGGGCGGGCTGCCGAGGGGCCAACCCGGGCGGGGCGGGCGCCGCGCCGGCGGCTAGCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52278395..52278625 26863196 MeRIP-seq:(Medium) rs1446413018 Functional Loss SNV dbSNP153 33..33 33 - - - 87502 RMVar_ID_87502 Human_SNP_ID_133245815 m1A Human chr3 + 52342911 52342911 52342911 AGATAGGTGTGAGGGTTCTGGCTGAATAGAACAGGTGGTGTTCAGAGTCCGAGGCTGGAGGAGCT AGATAGGTGTGAGGGTTCTGGCTGAATAGAACGGGTGGTGTTCAGAGTCCGAGGCTGGAGGAGCT A G DNAH1 Ensembl:ENSG00000114841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52342867..52343038 26863196 MeRIP-seq:(Medium) rs540983614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1104122 RMVar_hsa_circ_25719,RMVar_hsa_circ_123176,RMVar_hsa_circ_76208,RMVar_hsa_circ_99273,RMVar_hsa_circ_218629,RMVar_hsa_circ_218630,RMVar_hsa_circ_106842,RMVar_hsa_circ_119403,RMVar_hsa_circ_218632,RMVar_hsa_circ_218634,RMVar_hsa_circ_95815,RMVar_hsa_circ_218633,RMVar_hsa_circ_218631,RMVar_hsa_circ_266262,RMVar_hsa_circ_24614 87503 RMVar_ID_87503 Human_SNP_ID_133263608 m1A Human chr3 - 52402156 52402156 52402156 CCCAGCTGGAGAGTCCAGGCCCTGGGAATGGGAGGAACCAGGCCACATTCCTTCCATCGTGCCCT CCCAGCTGGAGAGTCCAGGCCCTGGGAATGGGTGGAACCAGGCCACATTCCTTCCATCGTGCCCT T A BAP1 Ensembl:ENSG00000163930 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402106..52402381 26863196 MeRIP-seq:(Medium) rs1420393402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248450,Human_RBP_ID_605382,Human_RBP_ID_5120770,Human_RBP_ID_26510446,Human_RBP_ID_27320904 Human_miRNA_ID_342714,Human_miRNA_ID_586896,Human_miRNA_ID_1695073 87504 RMVar_ID_87504 Human_SNP_ID_133263640 m1A Human chr3 + 52402268 52402268 52402268 CTGGTGAGGGCCACACGGCAAGAGTGGGCTGCAGAGTCAGGGCCAGCAGTCCTCACTGGCGCTTG CTGGTGAGGGCCACACGGCAAGAGTGGGCTGCGGAGTCAGGGCCAGCAGTCCTCACTGGCGCTTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:52402139..52402300 26863196 MeRIP-seq:(Medium) rs1559584490 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_478 87505 RMVar_ID_87505 Human_SNP_ID_133263806 m1A Human chr3 - 52402676 52402675 52402677 GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTACAGATTGATGACCAGAGAAGGACCCACAACTACG GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTA__GATTGATGACCAGAGAAGGACCCACAACTACG CTG C BAP1 Ensembl:ENSG00000163930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402626..52402675 26863196 MeRIP-seq:(Medium) rs1456503766 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_437913,Human_Splice_Rec_437919,Human_Splice_Rec_437951,Human_Splice_Rec_437959,Human_Splice_Rec_437965 87506 RMVar_ID_87506 Human_SNP_ID_133263868 m1A Human chr3 - 52402810 52402808 52402811 GGCTGAGATTGCAAACTATGAGGCGTGCCTCAAGGAGGAGGTAGAGAAGAGGAAGAAGTTCAAGG GGCTGAGATTGCAAACTATGAGGCGTGCCTC___GAGGAGGTAGAGAAGAGGAAGAAGTTCAAGG CCTT C BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52402801..52402825 26863196 MeRIP-seq:(Medium) rs1226165465 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_605389,Human_RBP_ID_1033814,Human_RBP_ID_17704363,Human_RBP_ID_18008232,Human_RBP_ID_19010554,Human_RBP_ID_19115716 Human_Splice_Rec_437910,Human_Splice_Rec_437911,Human_Splice_Rec_437917,Human_Splice_Rec_437948,Human_Splice_Rec_437949,Human_Splice_Rec_437957,Human_Splice_Rec_437963 Clinvar_Rec_479 87507 RMVar_ID_87507 Human_SNP_ID_133263880 m1A Human chr3 + 52402839 52402839 52402839 TCCTTGAGGCACGCCTCATAGTTTGCAATCTCAGCCTCCACACACTTCAGCAGTGCCAGCAGCTC TCCTTGAGGCACGCCTCATAGTTTGCAATCTCGGCCTCCACACACTTCAGCAGTGCCAGCAGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402771..52402889 26863196 MeRIP-seq:(Medium) rs753767419 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_480 87508 RMVar_ID_87508 Human_SNP_ID_133264007 m1A Human chr3 - 52403185 52403185 52403185 TGGAAGCCACGGACAGCAGAGAGAAGACGGGGATGGTGAGGCCTGGCGAGCCCTTGAGTGGGGAG TGGAAGCCACGGACAGCAGAGAGAAGACGGGGGTGGTGAGGCCTGGCGAGCCCTTGAGTGGGGAG T C BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52403126..52403250 26863196 MeRIP-seq:(Medium) rs1183229867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248454,Human_RBP_ID_5602707,Human_RBP_ID_7209590,Human_RBP_ID_19010555 Human_Splice_Rec_437909,Human_Splice_Rec_437947,Human_Splice_Rec_437955 Clinvar_Rec_481 87509 RMVar_ID_87509 Human_SNP_ID_133264023 m1A Human chr3 - 52403205 52403205 52403205 CCCAGTGGAGAAGGAGGTCGTGGAAGCCACGGACAGCAGAGAGAAGACGGGGATGGTGAGGCCTG CCCAGTGGAGAAGGAGGTCGTGGAAGCCACGGGCAGCAGAGAGAAGACGGGGATGGTGAGGCCTG T C BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:52403119..52403272;chr3:52403126..52403300 26863196 MeRIP-seq:(Medium) rs1391316596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_437908,Human_Splice_Rec_437909,Human_Splice_Rec_437946,Human_Splice_Rec_437947,Human_Splice_Rec_437954,Human_Splice_Rec_437955,Human_Splice_Rec_437962 87510 RMVar_ID_87510 Human_SNP_ID_133265965 m1A Human chr3 + 52408593 52408593 52408593 GCGCTCTTCGATCCATTTGAACAGGAAGATAAATCCATATACAGGGCTGGGGGAAGTAAGGGGCA GCGCTCTTCGATCCATTTGAACAGGAAGATAAGTCCATATACAGGGCTGGGGGAAGTAAGGGGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52408442..52408625 26863196 MeRIP-seq:(Medium) rs766998626 Functional Loss SNV dbSNP153 33..33 33 - - - 87511 RMVar_ID_87511 Human_SNP_ID_133266422 m1A Human chr3 - 52409881 52409881 52409881 CTGGACATGGCGCTGAGGGGCCGCCCCGCGGGAAGATGAATAAGGGCTGGCTGGAGCTGGAGAGC CTGGACATGGCGCTGAGGGGCCGCCCCGCGGGGAGATGAATAAGGGCTGGCTGGAGCTGGAGAGC T C BAP1 Ensembl:ENSG00000163930 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:52409630..52409925 26863196 MeRIP-seq:(Medium) rs1553646425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247607,Human_RBP_ID_936588,Human_RBP_ID_3964107,Human_RBP_ID_4756529,Human_RBP_ID_5120333,Human_RBP_ID_5393241,Human_RBP_ID_8236042,Human_RBP_ID_8576043,Human_RBP_ID_18423997,Human_RBP_ID_18953592,Human_RBP_ID_19012529 Human_Splice_Rec_437883,Human_Splice_Rec_437921,Human_Splice_Rec_437979,Human_Splice_Rec_437991 Human_miRNA_ID_2001295,Human_miRNA_ID_2002681,Human_miRNA_ID_2396968 Clinvar_Rec_482 RMVar_hsa_circ_95271,RMVar_hsa_circ_218645,RMVar_hsa_circ_115310,RMVar_hsa_circ_218648 87512 RMVar_ID_87512 Human_SNP_ID_133266440 m1A Human chr3 + 52409906 52409906 52409906 TTCATCTTCCCGCGGGGCGGCCCCTCAGCGCCATGTCCAGGCCCTCCCTCCCCACCGCTGCCCCC TTCATCTTCCCGCGGGGCGGCCCCTCAGCGCCCTGTCCAGGCCCTCCCTCCCCACCGCTGCCCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52409774..52409950 26863196 MeRIP-seq:(Medium) rs1202040640 Functional Loss SNV dbSNP153 33..33 33 - - - 87513 RMVar_ID_87513 Human_SNP_ID_133268025 m1A Human chr3 + 52415245 52415245 52415245 TGAGAACGGAGTCTCACTCTCTTGCCCAGGCTAGAGTGCAGTGGCGTGATCCCGGCTCACTGCAA TGAGAACGGAGTCTCACTCTCTTGCCCAGGCTGGAGTGCAGTGGCGTGATCCCGGCTCACTGCAA A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1453163087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115233,RMVar_hsa_circ_369935,RMVar_hsa_circ_218652,RMVar_hsa_circ_218654,RMVar_hsa_circ_76878,RMVar_hsa_circ_218653 87514 RMVar_ID_87514 Human_SNP_ID_133270169 m1A Human chr3 + 52423447 52423446 52423447 AGCAGGGCCAGCAGTGAGACTATGAGCCAAGCAAAGAGAAGTCTCAGTGGAGCATGAGGAGGGAG AGCAGGGCCAGCAGTGAGACTATGAGCCAAGC_AAGAGAAGTCTCAGTGGAGCATGAGGAGGGAG CA C PHF7 Ensembl:ENSG00000010318 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52423347..52423446 32194978 MeRIP-seq:(Medium) rs369376672 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_115233,RMVar_hsa_circ_218654,RMVar_hsa_circ_105765,RMVar_hsa_circ_218655 87515 RMVar_ID_87515 Human_SNP_ID_133272929 m1A Human chr3 + 52435645 52435645 52435645 TCCACCTCCCGGGGCGTCCGATTGTGCTCGGCATGCACCCGGCTCTTCATCTTCTTGCCTAGCTC TCCACCTCCCGGGGCGTCCGATTGTGCTCGGCGTGCACCCGGCTCTTCATCTTCTTGCCTAGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52435638..52435722 26863196 MeRIP-seq:(Medium) rs1298477697 Functional Loss SNV dbSNP153 33..33 33 - - - 87516 RMVar_ID_87516 Human_SNP_ID_133278867 m1A Human chr3 + 52455691 52455691 52455691 CTTCGGGCCCGAGCGGGAAGCCGAGCCGGCCAAGGAAGCGCGCGTCGTGGGCTCGGAGCTTGTGG CTTCGGGCCCGAGCGGGAAGCCGAGCCGGCCATGGAAGCGCGCGTCGTGGGCTCGGAGCTTGTGG A T NISCH Ensembl:ENSG00000010322 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:52455601..52455750 26863410 MeRIP-seq:(Medium) rs1159704460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782676,Human_RBP_ID_4757304,Human_RBP_ID_5206580,Human_RBP_ID_26763008 Human_Splice_Rec_438204,Human_Splice_Rec_438205,Human_Splice_Rec_438245,Human_Splice_Rec_438285,Human_Splice_Rec_438309 RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_218661 87517 RMVar_ID_87517 Human_SNP_ID_133278877 m1A Human chr3 - 52455731 52455731 52455731 CGCTTCGGGTGCCCGCGCCCCCAACACACCGTATAAGTGTCCACAAGCTCCGAGCCCACGACGCG CGCTTCGGGTGCCCGCGCCCCCAACACACCGTGTAAGTGTCCACAAGCTCCGAGCCCACGACGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:52455616..52455761 26863196 MeRIP-seq:(Medium) rs763465212 Functional Loss SNV dbSNP153 33..33 33 - - - 87518 RMVar_ID_87518 Human_SNP_ID_133286369 m1A Human chr3 + 52484451 52484451 52484451 CAGTAGCCTGAGGGGCCCAGCCCCACTTGTTGAACAGCCGCTCTCCCCGCCCCACCCACCCTGCC CAGTAGCCTGAGGGGCCCAGCCCCACTTGTTGCACAGCCGCTCTCCCCGCCCCACCCACCCTGCC A C NISCH Ensembl:ENSG00000010322 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52484419..52484551 26863196 MeRIP-seq:(Medium) rs1443149780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14891048 RMVar_hsa_circ_118954,RMVar_hsa_circ_218660,RMVar_hsa_circ_19804,RMVar_hsa_circ_124844,RMVar_hsa_circ_218672,RMVar_hsa_circ_113036,RMVar_hsa_circ_218675 87519 RMVar_ID_87519 Human_SNP_ID_133287215 m1A Human chr3 + 52487427 52487412 52487427 CAGGGCGAGGAGGAGGATGAGGAGGAGGAAGAAGAGGAGGACGTGGCTGAGAACCGCTACTTTGA CAGGGCGAGGAGGAGGAT_______________GAGGAGGACGTGGCTGAGAACCGCTACTTTGA TGAGGAGGAGGAAGAA T NISCH Ensembl:ENSG00000010322 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52487326..52487594 26863196 MeRIP-seq:(Medium) rs1226029843 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_5530499,Human_RBP_ID_14891093,Human_RBP_ID_22456707 RMVar_hsa_circ_118954,RMVar_hsa_circ_218660,RMVar_hsa_circ_19804,RMVar_hsa_circ_124844,RMVar_hsa_circ_218672,RMVar_hsa_circ_113036,RMVar_hsa_circ_81320,RMVar_hsa_circ_13236,RMVar_hsa_circ_218675,RMVar_hsa_circ_109418,RMVar_hsa_circ_218677,RMVar_hsa_circ_218678 87520 RMVar_ID_87520 Human_SNP_ID_133287215 m1A Human chr3 + 52487426 52487412 52487427 ACAGGGCGAGGAGGAGGATGAGGAGGAGGAAGAAGAGGAGGACGTGGCTGAGAACCGCTACTTTG ACAGGGCGAGGAGGAGGAT_______________GAGGAGGACGTGGCTGAGAACCGCTACTTTG TGAGGAGGAGGAAGAA T NISCH Ensembl:ENSG00000010322 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr3:52487310..52487601;chr3:52487401..52487551 26863196 MeRIP-seq:(Medium) rs1226029843 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_5530499,Human_RBP_ID_14891093,Human_RBP_ID_22456707 RMVar_hsa_circ_118954,RMVar_hsa_circ_218660,RMVar_hsa_circ_19804,RMVar_hsa_circ_124844,RMVar_hsa_circ_218672,RMVar_hsa_circ_113036,RMVar_hsa_circ_81320,RMVar_hsa_circ_13236,RMVar_hsa_circ_218675,RMVar_hsa_circ_109418,RMVar_hsa_circ_218677,RMVar_hsa_circ_218678 87521 RMVar_ID_87521 Human_SNP_ID_133287226 m1A Human chr3 + 52487427 52487427 52487427 CAGGGCGAGGAGGAGGATGAGGAGGAGGAAGAAGAGGAGGACGTGGCTGAGAACCGCTACTTTGA CAGGGCGAGGAGGAGGATGAGGAGGAGGAAGAGGAGGAGGACGTGGCTGAGAACCGCTACTTTGA A G NISCH Ensembl:ENSG00000010322 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52487326..52487594 26863196 MeRIP-seq:(Medium) rs767855101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530499,Human_RBP_ID_14891093,Human_RBP_ID_22456707 RMVar_hsa_circ_118954,RMVar_hsa_circ_218660,RMVar_hsa_circ_19804,RMVar_hsa_circ_124844,RMVar_hsa_circ_218672,RMVar_hsa_circ_113036,RMVar_hsa_circ_81320,RMVar_hsa_circ_13236,RMVar_hsa_circ_218675,RMVar_hsa_circ_109418,RMVar_hsa_circ_218677,RMVar_hsa_circ_218678 87522 RMVar_ID_87522 Human_SNP_ID_133287590 m1A Human chr3 - 52488223 52488223 52488223 CTTGATGACGTTGAGGTGCTGGGGCGTGAGCAACAGCCAGTAGGGGATGGCGGCGGACTTGACGG CTTGATGACGTTGAGGTGCTGGGGCGTGAGCACCAGCCAGTAGGGGATGGCGGCGGACTTGACGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52488173..52488400 26863196 MeRIP-seq:(Medium) rs200548649 Functional Loss SNV dbSNP153 33..33 33 - - - 87523 RMVar_ID_87523 Human_SNP_ID_133297709 m1A Human chr3 + 52519219 52519219 52519219 TCAACCTCCACCTCAGGCCCCGATAGCTTCCGAGCACCCCACCTATCTGCTTCATCAGCCCCGTG TCAACCTCCACCTCAGGCCCCGATAGCTTCCGGGCACCCCACCTATCTGCTTCATCAGCCCCGTG A G STAB1 Ensembl:ENSG00000010327 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52519190..52519290 26863196 MeRIP-seq:(Medium) rs1272291794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76704,RMVar_hsa_circ_218689,RMVar_hsa_circ_94714,RMVar_hsa_circ_218692,RMVar_hsa_circ_97809,RMVar_hsa_circ_90124,RMVar_hsa_circ_218698,RMVar_hsa_circ_218699 87524 RMVar_ID_87524 Human_SNP_ID_133300065 m1A Human chr3 - 52524487 52524487 52524487 CCGGCTGCATGAAGACCCCCTTCCTTGGTGACATGGCCCACATCCGCTGAGGGCACCTTTATTGT CCGGCTGCATGAAGACCCCCTTCCTTGGTGACGTGGCCCACATCCGCTGAGGGCACCTTTATTGT T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52524437..52524660 26863196 MeRIP-seq:(Medium) rs756366185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605486,Human_RBP_ID_4766734,Human_RBP_ID_5120334,Human_RBP_ID_17661483,Human_RBP_ID_27320981 Human_miRNA_ID_1337336,Human_miRNA_ID_1354202 87525 RMVar_ID_87525 Human_SNP_ID_133300082 m1A Human chr3 - 52524545 52524545 52524545 TACCCACGCCGTACGCCGCTGCAGCACGAGGCACCCCTCTGGATGGACCAGCTCTGCACCGGCTG TACCCACGCCGTACGCCGCTGCAGCACGAGGCGCCCCTCTGGATGGACCAGCTCTGCACCGGCTG T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52524426..52524750 26863196 MeRIP-seq:(Medium) rs367968712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605486,Human_RBP_ID_1965604,Human_RBP_ID_8873525,Human_RBP_ID_14891176,Human_RBP_ID_17403934,Human_RBP_ID_24428091,Human_RBP_ID_24498559,Human_RBP_ID_27056989,Human_RBP_ID_27320982 Human_Splice_Rec_438694,Human_Splice_Rec_438700 87526 RMVar_ID_87526 Human_SNP_ID_133300126 m1A Human chr3 + 52524635 52524635 52524635 AGCAGGCAGCTGAGGGAGGCCATGTAGAGGTCAGAGAAGCGCACGAGGCGCCTTGAGAAGTAGGT AGCAGGCAGCTGAGGGAGGCCATGTAGAGGTCGGAGAAGCGCACGAGGCGCCTTGAGAAGTAGGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:52524484..52524722 26863196 MeRIP-seq:(Medium) rs1423945901 Functional Loss SNV dbSNP153 33..33 33 - - - 87527 RMVar_ID_87527 Human_SNP_ID_133300340 m1A Human chr3 - 52525012 52525012 52525012 GATCCGCATCATCAACACGGAGCAGTACATGCACTCGCTGACGTGGCAGCAGGCGCTCACGGGGC GATCCGCATCATCAACACGGAGCAGTACATGCGCTCGCTGACGTGGCAGCAGGCGCTCACGGGGC T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52524882..52525047 26863196 MeRIP-seq:(Medium) rs754871503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605498,Human_RBP_ID_1965606,Human_RBP_ID_4749553,Human_RBP_ID_8873527,Human_RBP_ID_19012560 Human_Splice_Rec_438690,Human_Splice_Rec_438691,Human_Splice_Rec_438696,Human_Splice_Rec_438697,Human_Splice_Rec_438722,Human_Splice_Rec_438723,Human_Splice_Rec_438748,Human_Splice_Rec_438749,Human_Splice_Rec_438754,Human_Splice_Rec_438755,Human_Splice_Rec_438778,Human_Splice_Rec_438779,Human_Splice_Rec_438802,Human_Splice_Rec_438803,Human_Splice_Rec_438812,Human_Splice_Rec_438813,Human_Splice_Rec_438824 RMVar_hsa_circ_57122 87528 RMVar_ID_87528 Human_SNP_ID_133300391 m1A Human chr3 + 52525093 52525093 52525093 GGATGATGGCGCCTGTGCGCCAGCCGTGCCGCAGCATGAGATCCTGGTGGGTGGGGCGGCAGAAC GGATGATGGCGCCTGTGCGCCAGCCGTGCCGCGGCATGAGATCCTGGTGGGTGGGGCGGCAGAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52524966..52525270 32194978 MeRIP-seq:(Medium) rs1412630351 Functional Loss SNV dbSNP153 33..33 33 - - - 87529 RMVar_ID_87529 Human_SNP_ID_133301917 m1A Human chr3 - 52529277 52529277 52529277 TCTCCTGAACCCAGCAGCCATCTACGCCAACAACGAGATCAGCCTGCGTGACGTTGAGGTCTACG TCTCCTGAACCCAGCAGCCATCTACGCCAACAGCGAGATCAGCCTGCGTGACGTTGAGGTCTACG T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52529226..52529932 26863196 MeRIP-seq:(Medium) rs757803797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1965622,Human_RBP_ID_4766769,Human_RBP_ID_18811743,Human_RBP_ID_23189880 Human_Splice_Rec_438702,Human_Splice_Rec_438728,Human_Splice_Rec_438760,Human_Splice_Rec_438784,Human_Splice_Rec_438826,Human_Splice_Rec_438848,Human_Splice_Rec_438860,Human_Splice_Rec_438868 RMVar_hsa_circ_52261,RMVar_hsa_circ_57122,RMVar_hsa_circ_106353,RMVar_hsa_circ_332943,RMVar_hsa_circ_116525,RMVar_hsa_circ_218702,RMVar_hsa_circ_218703,RMVar_hsa_circ_218704,RMVar_hsa_circ_53188 87530 RMVar_ID_87530 Human_SNP_ID_133301926 m1A Human chr3 - 52529302 52529302 52529302 ACCTCCTGCCCCCCGAGGTCTGCAGTCTCCTGAACCCAGCAGCCATCTACGCCAACAACGAGATC ACCTCCTGCCCCCCGAGGTCTGCAGTCTCCTGCACCCAGCAGCCATCTACGCCAACAACGAGATC T G NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr3:52529201..52529417;chr3:52529251..52532199 26863196 MeRIP-seq:(Medium) rs1407580848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4766770,Human_RBP_ID_5209918,Human_RBP_ID_8576131 Human_Splice_Rec_438702,Human_Splice_Rec_438728,Human_Splice_Rec_438760,Human_Splice_Rec_438784,Human_Splice_Rec_438826,Human_Splice_Rec_438848,Human_Splice_Rec_438860,Human_Splice_Rec_438868 RMVar_hsa_circ_52261,RMVar_hsa_circ_57122,RMVar_hsa_circ_106353,RMVar_hsa_circ_332943,RMVar_hsa_circ_116525,RMVar_hsa_circ_218702,RMVar_hsa_circ_218703,RMVar_hsa_circ_218704,RMVar_hsa_circ_53188 87531 RMVar_ID_87531 Human_SNP_ID_133302974 m1A Human chr3 - 52533554 52533554 52533554 CCGCCCAGGCACCCACCAGCGGCGCCGACCTCAGCGCGCACCTATGGGCTCGCTACCAGGACATG CCGCCCAGGCACCCACCAGCGGCGCCGACCTCGGCGCGCACCTATGGGCTCGCTACCAGGACATG T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:52533445..52533825 26863196 MeRIP-seq:(Medium) rs1214815297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155781,Human_RBP_ID_605533,Human_RBP_ID_4758101,Human_RBP_ID_8873549,Human_RBP_ID_24011064 Human_Splice_Rec_438701,Human_Splice_Rec_438759,Human_Splice_Rec_438825 RMVar_hsa_circ_106353,RMVar_hsa_circ_116525,RMVar_hsa_circ_218703,RMVar_hsa_circ_218704 87532 RMVar_ID_87532 Human_SNP_ID_133302994 m1A Human chr3 + 52533601 52533601 52533601 TGGTGGGTGCCTGGGCGGGCGCGGAGCGCGGGACGCCGGGGCAGTGGGCGCCGGGACCCGGGGGG TGGTGGGTGCCTGGGCGGGCGCGGAGCGCGGGGCGCCGGGGCAGTGGGCGCCGGGACCCGGGGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr3:52533446..52533725;chr3:52533437..52534218 26863196 MeRIP-seq:(Medium) rs66782572 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10715,GWAS_ID_10716,GWAS_ID_10717,GWAS_ID_10718,GWAS_ID_10719,GWAS_ID_10720,GWAS_ID_10721,GWAS_ID_10722,GWAS_ID_10723,GWAS_ID_10724,GWAS_ID_10725,GWAS_ID_10726,GWAS_ID_10727,GWAS_ID_10728,GWAS_ID_10729,GWAS_ID_10730,GWAS_ID_10731,GWAS_ID_10732,GWAS_ID_10733,GWAS_ID_10734,GWAS_ID_10735,GWAS_ID_10736,GWAS_ID_10737,GWAS_ID_10738,GWAS_ID_10739,GWAS_ID_10740,GWAS_ID_10741,GWAS_ID_10742,GWAS_ID_10743,GWAS_ID_10744,GWAS_ID_10745,GWAS_ID_10746,GWAS_ID_10747,GWAS_ID_10748,GWAS_ID_10749,GWAS_ID_10750,GWAS_ID_10751,GWAS_ID_10752,GWAS_ID_10753,GWAS_ID_10754,GWAS_ID_10755,GWAS_ID_10756,GWAS_ID_10757 87533 RMVar_ID_87533 Human_SNP_ID_133303076 m1A Human chr3 - 52533767 52533767 52533767 GGCGGGCGGCGGGCGGCGGGCTGGCCGAGGGCAGCGCGGGCGGCGGGCGGCGCGCGGTGGGCATG GGCGGGCGGCGGGCGGCGGGCTGGCCGAGGGCTGCGCGGGCGGCGGGCGGCGCGCGGTGGGCATG T A NT5DC2 Ensembl:ENSG00000168268 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:52533576..52533850 26863196 MeRIP-seq:(Medium) rs1307199689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247736,Human_RBP_ID_783882,Human_RBP_ID_836828,Human_RBP_ID_4756537,Human_RBP_ID_5241702,Human_RBP_ID_5393265,Human_RBP_ID_8209323,Human_RBP_ID_8729775,Human_RBP_ID_9434636,Human_RBP_ID_18424235,Human_RBP_ID_18464418,Human_RBP_ID_19117774,Human_RBP_ID_21987008,Human_RBP_ID_22418279,Human_RBP_ID_24554031,Human_RBP_ID_26790144 RMVar_hsa_circ_106353,RMVar_hsa_circ_116525,RMVar_hsa_circ_218703,RMVar_hsa_circ_218704 87534 RMVar_ID_87534 Human_SNP_ID_133304014 m1A Human chr3 + 52536667 52536667 52536667 ACGGCGCTCGCTAGTCTCCCAGGTCGCGGTACACGGCGAGAACGGGCGGGGCGGTCTCGGCTGCG ACGGCGCTCGCTAGTCTCCCAGGTCGCGGTACTCGGCGAGAACGGGCGGGGCGGTCTCGGCTGCG A T SMIM4 Ensembl:ENSG00000168273 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1242109872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757305,Human_RBP_ID_5447752,Human_RBP_ID_5474465,Human_RBP_ID_5506637 87535 RMVar_ID_87535 Human_SNP_ID_133304644 m1A Human chr3 - 52539347 52539347 52539347 CCTCCTGTCCTTGGACCTCACGTTTCTTCCCCAGGTCCTTGGCCCCGTCTTACCCGCTCAGCCGC CCTCCTGTCCTTGGACCTCACGTTTCTTCCCCGGGTCCTTGGCCCCGTCTTACCCGCTCAGCCGC T C lnc-NT5DC2-1 RNACentral:URS00008B5074 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52539342..52539434 26863196 MeRIP-seq:(Medium) rs756376103 Functional Loss SNV dbSNP153 33..33 33 - - - 87536 RMVar_ID_87536 Human_SNP_ID_133304881 m1A Human chr3 + 52540406 52540406 52540406 AATTTTAAATATGTTTCTTAAACATCTGAGCAACTTTTTGTTTGATACAGATGATGTCTACCGTA AATTTTAAATATGTTTCTTAAACATCTGAGCAGCTTTTTGTTTGATACAGATGATGTCTACCGTA A G SMIM4 Ensembl:ENSG00000168273 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52540401..52540450 26863196 MeRIP-seq:(Medium) rs1444599835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15002355,Human_RBP_ID_25745385 87537 RMVar_ID_87537 Human_SNP_ID_133340194 m1A Human chr3 - 52679723 52679720 52679723 GTAAGAACATGGCTGATTATTTCTTATAGAAGAAGTTGGATTCCATGGGTTCCAAGAGAAGAAGA GTAAGAACATGGCTGATTATTTCTTATAGAAG___TTGGATTCCATGGGTTCCAAGAGAAGAAGA ACTT A PBRM1 Ensembl:ENSG00000163939 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52679699..52679780 26863196 MeRIP-seq:(Medium) rs1561149393 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_935453,Human_RBP_ID_2790891,Human_RBP_ID_3964127,Human_RBP_ID_8236047,Human_RBP_ID_9393756,Human_RBP_ID_14893200,Human_RBP_ID_19010595 Human_Splice_Rec_438938,Human_Splice_Rec_439486,Human_Splice_Rec_439500,Human_Splice_Rec_439508,Human_Splice_Rec_439516,Human_Splice_Rec_439526,Human_Splice_Rec_439532,Human_Splice_Rec_439540 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_352306,RMVar_hsa_circ_45061,RMVar_hsa_circ_14249,RMVar_hsa_circ_48261,RMVar_hsa_circ_111221,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_299690,RMVar_hsa_circ_218723,RMVar_hsa_circ_360476,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_309126,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_35685,RMVar_hsa_circ_33167,RMVar_hsa_circ_218764,RMVar_hsa_circ_218752,RMVar_hsa_circ_120215,RMVar_hsa_circ_332668,RMVar_hsa_circ_349510,RMVar_hsa_circ_318672,RMVar_hsa_circ_218750,RMVar_hsa_circ_218751,RMVar_hsa_circ_293106,RMVar_hsa_circ_298720,RMVar_hsa_circ_218753,RMVar_hsa_circ_218759,RMVar_hsa_circ_301757,RMVar_hsa_circ_317816,RMVar_hsa_circ_338034,RMVar_hsa_circ_309271,RMVar_hsa_circ_218760,RMVar_hsa_circ_218757,RMVar_hsa_circ_218758,RMVar_hsa_circ_46295,RMVar_hsa_circ_314612,RMVar_hsa_circ_325776,RMVar_hsa_circ_360628,RMVar_hsa_circ_218762,RMVar_hsa_circ_218763,RMVar_hsa_circ_293695,RMVar_hsa_circ_218761,RMVar_hsa_circ_279744,RMVar_hsa_circ_66719,RMVar_hsa_circ_282016,RMVar_hsa_circ_291508,RMVar_hsa_circ_309743,RMVar_hsa_circ_276964,RMVar_hsa_circ_218765,RMVar_hsa_circ_218767,RMVar_hsa_circ_218768,RMVar_hsa_circ_218766,RMVar_hsa_circ_12920 87538 RMVar_ID_87538 Human_SNP_ID_133341925 m1A Human chr3 + 52685866 52685866 52685866 CCTCCGGCCGCGGCCGCTGCCGTCGCTTCGGCACCCGCCGCCCTCACCTCCCTTACCCCTCCCGG CCTCCGGCCGCGGCCGCTGCCGTCGCTTCGGCCCCCGCCGCCCTCACCTCCCTTACCCCTCCCGG A C GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52685711..52685950 26863196 MeRIP-seq:(Medium) rs1182353621 Functional Loss SNV dbSNP153 33..33 33 - - - 87539 RMVar_ID_87539 Human_SNP_ID_133341926 m1A Human chr3 + 52685866 52685866 52685866 CCTCCGGCCGCGGCCGCTGCCGTCGCTTCGGCACCCGCCGCCCTCACCTCCCTTACCCCTCCCGG CCTCCGGCCGCGGCCGCTGCCGTCGCTTCGGCTCCCGCCGCCCTCACCTCCCTTACCCCTCCCGG A T GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52685711..52685950 26863196 MeRIP-seq:(Medium) rs1182353621 Functional Loss SNV dbSNP153 33..33 33 - - - 87540 RMVar_ID_87540 Human_SNP_ID_133341934 m1A Human chr3 - 52685877 52685877 52685877 TTGCGGCGGCACCGGGAGGGGTAAGGGAGGTGAGGGCGGCGGGTGCCGAAGCGACGGCAGCGGCC TTGCGGCGGCACCGGGAGGGGTAAGGGAGGTGCGGGCGGCGGGTGCCGAAGCGACGGCAGCGGCC T G PBRM1 Ensembl:ENSG00000163939 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:52685755..52685900 26863196 MeRIP-seq:(Medium) rs950739317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11487,Human_RBP_ID_4756539,Human_RBP_ID_8875540,Human_RBP_ID_9434637,Human_RBP_ID_18424414,Human_RBP_ID_18953597,Human_RBP_ID_22456708 87541 RMVar_ID_87541 Human_SNP_ID_133342059 m1A Human chr3 + 52686091 52686091 52686091 GGTTGATGTGTTTGTGCTTCCTTCTACAGCCAATATGAAAAGGCCTAGTAAGTGGGGTCGGGAGG GGTTGATGTGTTTGTGCTTCCTTCTACAGCCACTATGAAAAGGCCTAGTAAGTGGGGTCGGGAGG A C GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:52686026..52686161;chr3:52686026..52686160 26863196 MeRIP-seq:(Medium) rs1247340002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1629639,Human_RBP_ID_4757309 Human_Splice_Rec_439551,Human_Splice_Rec_439589,Human_Splice_Rec_439591,Human_Splice_Rec_439597,Human_Splice_Rec_439609,Human_Splice_Rec_439637 87542 RMVar_ID_87542 Human_SNP_ID_133344065 m1A Human chr3 - 52692917 52692915 52692917 GAATTAAGTGGAGATACGATGAAGCTCGGACTATCTATGATTGTGATCTGTTTGTCCAAGGGGAC GAATTAAGTGGAGATACGATGAAGCTCGGACT__CTATGATTGTGATCTGTTTGTCCAAGGGGAC GAT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:52692832..52693050 26863196 MeRIP-seq:(Medium) rs759360561 Functional Loss DEL dbSNP153 33..34 33 - - - 87543 RMVar_ID_87543 Human_SNP_ID_133344066 m1A Human chr3 - 52692917 52692917 52692917 GAATTAAGTGGAGATACGATGAAGCTCGGACTATCTATGATTGTGATCTGTTTGTCCAAGGGGAC GAATTAAGTGGAGATACGATGAAGCTCGGACTGTCTATGATTGTGATCTGTTTGTCCAAGGGGAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:52692832..52693050 26863196 MeRIP-seq:(Medium) rs753352133 Functional Loss SNV dbSNP153 33..33 33 - - - 87544 RMVar_ID_87544 Human_SNP_ID_133344076 m1A Human chr3 - 52692927 52692927 52692927 CGCAGAGGAGGAATTAAGTGGAGATACGATGAAGCTCGGACTATCTATGATTGTGATCTGTTTGT CGCAGAGGAGGAATTAAGTGGAGATACGATGATGCTCGGACTATCTATGATTGTGATCTGTTTGT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:52692807..52693052 26863196 MeRIP-seq:(Medium) rs1025140062 Functional Loss SNV dbSNP153 33..33 33 - - - 87545 RMVar_ID_87545 Human_SNP_ID_133344077 m1A Human chr3 - 52692927 52692927 52692927 CGCAGAGGAGGAATTAAGTGGAGATACGATGAAGCTCGGACTATCTATGATTGTGATCTGTTTGT CGCAGAGGAGGAATTAAGTGGAGATACGATGACGCTCGGACTATCTATGATTGTGATCTGTTTGT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:52692807..52693052 26863196 MeRIP-seq:(Medium) rs1025140062 Functional Loss SNV dbSNP153 33..33 33 - - - 87546 RMVar_ID_87546 Human_SNP_ID_133344227 m1A Human chr3 + 52693305 52693305 52693305 AGGTGGAATCCCAAATGTTGAAGGTGCTGCCAAACTGCTGTGGTCTGAGTGGACAGGGTAAGCTT AGGTGGAATCCCAAATGTTGAAGGTGCTGCCAGACTGCTGTGGTCTGAGTGGACAGGGTAAGCTT A G GNL3 Ensembl:ENSG00000163938 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52692973..52693394 32194978 MeRIP-seq:(Medium) rs1220550427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605697,Human_RBP_ID_1629729,Human_RBP_ID_1965810,Human_RBP_ID_2790960,Human_RBP_ID_3712007,Human_RBP_ID_7210348,Human_RBP_ID_8873712,Human_RBP_ID_14893807,Human_RBP_ID_17290678,Human_RBP_ID_18811904,Human_RBP_ID_22824684,Human_RBP_ID_23135397,Human_RBP_ID_24011359,Human_RBP_ID_26347000 Human_Splice_Rec_439581,Human_Splice_Rec_439629,Human_Splice_Rec_439655 RMVar_hsa_circ_326,RMVar_hsa_circ_71418,RMVar_hsa_circ_17945,RMVar_hsa_circ_348884,RMVar_hsa_circ_51460 87547 RMVar_ID_87547 Human_SNP_ID_133344413 m1A Human chr3 + 52693737 52693734 52693738 AAAGGACATACATGAAGAATTGCCAAAACGGAAAGAAAGGAAGCAGGAGGAGAGGGAGGATGACA AAAGGACATACATGAAGAATTGCCAAAACG____GAAAGGAAGCAGGAGGAGAGGGAGGATGACA GGAAA G GNL3 Ensembl:ENSG00000163938 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:52693686..52693829;chr3:52693686..52693825 26863196 MeRIP-seq:(Medium) rs1561259436 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_68568,Human_RBP_ID_1965814,Human_RBP_ID_2790976,Human_RBP_ID_4750004,Human_RBP_ID_7210358,Human_RBP_ID_9141927,Human_RBP_ID_9393763,Human_RBP_ID_14893833,Human_RBP_ID_17292048,Human_RBP_ID_21897539,Human_RBP_ID_22677965,Human_RBP_ID_23115893,Human_RBP_ID_24547406,Human_RBP_ID_25745799,Human_RBP_ID_26347002,Human_RBP_ID_27822327 Human_Splice_Rec_439585,Human_Splice_Rec_439633,Human_Splice_Rec_439659 RMVar_hsa_circ_71418,RMVar_hsa_circ_348884,RMVar_hsa_circ_310167,RMVar_hsa_circ_51460,RMVar_hsa_circ_218773 87548 RMVar_ID_87548 Human_SNP_ID_133347664 m1A Human chr3 + 52705645 52705645 52705645 TGCCAGCTCAGCGCCCGCGCCGCAGGCCCCGGAGCCCAGCCCGTTGTCTGGCCGCCCGCGTTCCC TGCCAGCTCAGCGCCCGCGCCGCAGGCCCCGGCGCCCAGCCCGTTGTCTGGCCGCCCGCGTTCCC A C SPCS1 Ensembl:ENSG00000114902 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52705463..52705750 26863196 MeRIP-seq:(Medium) rs1198488036 Functional Loss SNV dbSNP153 33..33 33 - - - 87549 RMVar_ID_87549 Human_SNP_ID_133347900 m1A Human chr3 + 52706152 52706152 52706152 CCCGGGCTTAGAAGGCCCGGCTACTGACGCGCAGTGCCAGACCTTACCCCTCACGGTCCTTAAGT CCCGGGCTTAGAAGGCCCGGCTACTGACGCGCGGTGCCAGACCTTACCCCTCACGGTCCTTAAGT A G SPCS1 Ensembl:ENSG00000114902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:52706101..52706300 26863196 MeRIP-seq:(Medium) rs981415507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157528,Human_RBP_ID_605764,Human_RBP_ID_4750068 87550 RMVar_ID_87550 Human_SNP_ID_133347930 m1A Human chr3 - 52706179 52706179 52706179 GCAGGCTGCGAGGCGAGGGCGACCGAGACTTAAGGACCGTGAGGGGTAAGGTCTGGCACTGCGCG GCAGGCTGCGAGGCGAGGGCGACCGAGACTTAGGGACCGTGAGGGGTAAGGTCTGGCACTGCGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52706078..52706178 32194978 MeRIP-seq:(Medium) rs1386614254 Functional Loss SNV dbSNP153 33..33 33 - - - 87551 RMVar_ID_87551 Human_SNP_ID_133347986 m1A Human chr3 + 52706278 52706278 52706278 CATGCTGGAGCATCTGAGCTCGCTGCCCACGCAGATGGTGAGGGCGCAACCCGGGGACCTCTGCA CATGCTGGAGCATCTGAGCTCGCTGCCCACGCGGATGGTGAGGGCGCAACCCGGGGACCTCTGCA A G SPCS1 Ensembl:ENSG00000114902 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52706227..52706327 32194978 MeRIP-seq:(Medium) rs1411726681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605765,Human_RBP_ID_4756544,Human_RBP_ID_8943555,Human_RBP_ID_17661484,Human_RBP_ID_19115758 Human_Splice_Rec_439845,Human_Splice_Rec_439851,Human_Splice_Rec_439857 87552 RMVar_ID_87552 Human_SNP_ID_133348195 m1A Human chr3 + 52706845 52706845 52706845 GTACGTGGCTGAACAGTTCGGGTGGACTGTCTATATAGTTATGGCCGGATTTGCTTTTTCATGTT GTACGTGGCTGAACAGTTCGGGTGGACTGTCTGTATAGTTATGGCCGGATTTGCTTTTTCATGTT A G SPCS1 Ensembl:ENSG00000114902 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52706776..52706914 32194978 MeRIP-seq:(Medium) rs778072787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_605773,Human_RBP_ID_784396,Human_RBP_ID_934410,Human_RBP_ID_4757318,Human_RBP_ID_14894099,Human_RBP_ID_22456710,Human_RBP_ID_22768630,Human_RBP_ID_24011410,Human_RBP_ID_24498613 Human_Splice_Rec_439842,Human_Splice_Rec_439843,Human_Splice_Rec_439848,Human_Splice_Rec_439849,Human_Splice_Rec_439854,Human_Splice_Rec_439855,Human_Splice_Rec_439860,Human_Splice_Rec_439862,Human_Splice_Rec_439863 87553 RMVar_ID_87553 Human_SNP_ID_133348464 m1A Human chr3 + 52707749 52707749 52707749 CGGCATCCTCTCAAGTGGTTACCTGTTCAAGAATCAAGCACAGACGACAAGAAACCAGGGGAAAG CGGCATCCTCTCAAGTGGTTACCTGTTCAAGAGTCAAGCACAGACGACAAGAAACCAGGGGAAAG A G SPCS1 Ensembl:ENSG00000114902 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52707660..52707787 26863196 MeRIP-seq:(Medium) rs773233169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67324,Human_RBP_ID_1629784,Human_RBP_ID_1965840,Human_RBP_ID_3712031,Human_RBP_ID_7210408,Human_RBP_ID_14894132,Human_RBP_ID_17290692,Human_RBP_ID_17704393,Human_RBP_ID_18811928,Human_RBP_ID_22769830,Human_RBP_ID_26823945,Human_RBP_ID_27321139 Human_Splice_Rec_439844,Human_Splice_Rec_439850,Human_Splice_Rec_439856,Human_Splice_Rec_439864 Human_miRNA_ID_2236207 RMVar_hsa_circ_117302,RMVar_hsa_circ_218782 87554 RMVar_ID_87554 Human_SNP_ID_133364648 m1A Human chr3 - 52770884 52770884 52770884 TATGGCAGCGGCGTCGTCGCGGGCCGGGCCCCAGCAATCCCGCCCGGGCCCGGCTGCCTCAACAG TATGGCAGCGGCGTCGTCGCGGGCCGGGCCCCCGCAATCCCGCCCGGGCCCGGCTGCCTCAACAG T G NEK4 Ensembl:ENSG00000114904 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:52770801..52770888 26863410 MeRIP-seq:(Medium) rs1052822211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757319 87555 RMVar_ID_87555 Human_SNP_ID_133421709 m1A Human chr3 - 52992097 52992097 52992097 ACAGCAATGGGCAGAAGCCATAGGGACTTTGCAGCAGGTTAAGGACAGGCTTTGTGGCGGAGCTG ACAGCAATGGGCAGAAGCCATAGGGACTTTGCCGCAGGTTAAGGACAGGCTTTGTGGCGGAGCTG T G SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52992095..52992239 26863196 MeRIP-seq:(Medium) rs956963482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 87556 RMVar_ID_87556 Human_SNP_ID_133428303 m1A Human chr3 + 53018499 53018499 53018499 TGTTCTACACCCCTATCTACCATAACAGTCCCATAAGATCAGCACACAAACAGGCTCTCATGTTG TGTTCTACACCCCTATCTACCATAACAGTCCCGTAAGATCAGCACACAAACAGGCTCTCATGTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53018495..53018666 26863196 MeRIP-seq:(Medium) rs898063872 Functional Loss SNV dbSNP153 33..33 33 - - - 87557 RMVar_ID_87557 Human_SNP_ID_133435294 m1A Human chr3 - 53046429 53046429 53046429 AGGTGAGGCGCAGGCTGGATCGGGGCTGGGCCAGGGCGGGCACTGGGTTCCCGGGGACGCGTCTC AGGTGAGGCGCAGGCTGGATCGGGGCTGGGCCCGGGCGGGCACTGGGTTCCCGGGGACGCGTCTC T G SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:53046410..53046655 26863196 MeRIP-seq:(Medium) rs1176788463 Functional Loss SNV dbSNP153 33..33 33 - - - 87558 RMVar_ID_87558 Human_SNP_ID_133445837 m1A Human chr3 + 53087361 53087361 53087361 TAGGCCAGGGATCATGCTGCCCCTGATTTCCCACTGTGAACTGAACTCCATCCATCCCAGAGGCC TAGGCCAGGGATCATGCTGCCCCTGATTTCCCTCTGTGAACTGAACTCCATCCATCCCAGAGGCC A T HSALNG0026210 RNACentral:URS0000EC115F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53087353..53087435 26863196 MeRIP-seq:(Medium) rs115063752 Functional Loss SNV dbSNP153 33..33 33 - - - 87559 RMVar_ID_87559 Human_SNP_ID_133454474 m1A Human chr3 - 53122395 53122395 53122395 CTAGGAGAGCCCTTTTGGGTCTTGGCACAAGCACATATGTTTGTGAAGCTCAAGGTCAGTGCACC CTAGGAGAGCCCTTTTGGGTCTTGGCACAAGCGCATATGTTTGTGAAGCTCAAGGTCAGTGCACC T C RFT1 Ensembl:ENSG00000163933 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:53122391..53122492 32194978 MeRIP-seq:(Medium) rs1388260881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7211291 Human_Splice_Rec_440853,Human_Splice_Rec_440875,Human_Splice_Rec_440907 Human_miRNA_ID_2236208 RMVar_hsa_circ_4791,RMVar_hsa_circ_78823,RMVar_hsa_circ_58649,RMVar_hsa_circ_93911,RMVar_hsa_circ_218858,RMVar_hsa_circ_218859,RMVar_hsa_circ_218861,RMVar_hsa_circ_97807,RMVar_hsa_circ_355379,RMVar_hsa_circ_22669 87560 RMVar_ID_87560 Human_SNP_ID_133456413 m1A Human chr3 - 53130394 53130394 53130394 TGGTGTCTGAGCCTGGCGCGGAGGCTATGGGCAGCCAGGAGGTGCTGGGCCACGCGGCCCGGCTG TGGTGTCTGAGCCTGGCGCGGAGGCTATGGGCGGCCAGGAGGTGCTGGGCCACGCGGCCCGGCTG T C RFT1 Ensembl:ENSG00000163933 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:53125968..53130412;chr3:53130229..53130396 26863196 MeRIP-seq:(Medium) rs1201237484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248460,Human_RBP_ID_4756554,Human_RBP_ID_19115771 Human_Splice_Rec_440847,Human_Splice_Rec_440871,Human_Splice_Rec_440901 87561 RMVar_ID_87561 Human_SNP_ID_133462446 m1A Human chr3 + 53156337 53156337 53156337 GACTCTCCCTCTTCCCCTCTCATCCCATATCCAGCCCCCAGTCCTCAAGGTCTTCTCAGAGGTTC GACTCTCCCTCTTCCCCTCTCATCCCATATCCTGCCCCCAGTCCTCAAGGTCTTCTCAGAGGTTC A T PRKCD Ensembl:ENSG00000163932 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53156335..53156403 26863196 MeRIP-seq:(Medium) rs1216392340 Functional Loss SNV dbSNP153 33..33 33 - - - 87562 RMVar_ID_87562 Human_SNP_ID_133463657 m1A Human chr3 - 53161311 53161311 53161311 GGCGCTGACTGGGATGGGCCAAGCGGCCAGTGAGGTGTGGCCCGGGCCTCCGCGCGGCGGGCGGG GGCGCTGACTGGGATGGGCCAAGCGGCCAGTGGGGTGTGGCCCGGGCCTCCGCGCGGCGGGCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53161261..53161397 26863196 MeRIP-seq:(Medium) rs1388472444 Functional Loss SNV dbSNP153 33..33 33 - - - 87563 RMVar_ID_87563 Human_SNP_ID_133463689 m1A Human chr3 - 53161412 53161412 53161412 CCCGGCCCTCACTTACCTCCCGTTGCAGGGGCAGGCGCCAAGGGTCGCGGCGGCAGCGGCGGGGG CCCGGCCCTCACTTACCTCCCGTTGCAGGGGCCGGCGCCAAGGGTCGCGGCGGCAGCGGCGGGGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:53161238..53161450 26863196 MeRIP-seq:(Medium) rs1553662923 Functional Loss SNV dbSNP153 33..33 33 - - - 87564 RMVar_ID_87564 Human_SNP_ID_133465566 m1A Human chr3 + 53168910 53168900 53168910 GAGGAGTCTGGGCTTGTCAGAGGGGCAATGGGAGGCACTGGGGGCTTGGGCAGGGGGTGACAAAA GAGGAGTCTGGGCTTGTCAGAGG__________GGCACTGGGGGCTTGGGCAGGGGGTGACAAAA GGGCAATGGGA G PRKCD Ensembl:ENSG00000163932 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53168906..53169038 26863196 MeRIP-seq:(Medium) rs1269274827 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_8209328,Human_RBP_ID_17195135 RMVar_hsa_circ_90673,RMVar_hsa_circ_23726,RMVar_hsa_circ_218862 87565 RMVar_ID_87565 Human_SNP_ID_133465628 m1A Human chr3 + 53169145 53169145 53169145 TGGGGAGCAGGGGGAGCTGTCTGGCCTGAGCCACTGCCTGAGCTCGTGCACTCCTAGTGGATGAG TGGGGAGCAGGGGGAGCTGTCTGGCCTGAGCCGCTGCCTGAGCTCGTGCACTCCTAGTGGATGAG A G PRKCD Ensembl:ENSG00000163932 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53169138..53169281 26863196 MeRIP-seq:(Medium) rs776295020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721354 RMVar_hsa_circ_90673,RMVar_hsa_circ_23726,RMVar_hsa_circ_218862 87566 RMVar_ID_87566 Human_SNP_ID_133471617 m1A Human chr3 + 53192288 53192288 53192288 TGGAAGATTGAGGTTCCTGGACAGATCAGGCTAGCCCTGCCCTCCACCCACACCTGCCCGCTCCC TGGAAGATTGAGGTTCCTGGACAGATCAGGCTGGCCCTGCCCTCCACCCACACCTGCCCGCTCCC A G PRKCD Ensembl:ENSG00000163932 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53192238..53192392 26863196 MeRIP-seq:(Medium) rs372770730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606015 87567 RMVar_ID_87567 Human_SNP_ID_133479943 m1A Human chr3 + 53225700 53225700 53225700 TATTTACCCCTCCTCTCAGTACATCTTTGAGCACCTTTCCCAGAATCTCAGGAATGTATAGACCC TATTTACCCCTCCTCTCAGTACATCTTTGAGCCCCTTTCCCAGAATCTCAGGAATGTATAGACCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:53225651..53225750 26863196 MeRIP-seq:(Medium) rs1444040046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14899728 87568 RMVar_ID_87568 Human_SNP_ID_133480449 m1A Human chr3 - 53227357 53227356 53227357 AGAGGAGTCCATCCCCAGGCAGGGGGAGACCCAGGGGGGTGAGCTTTAAGCAGGGCCTGGCAAGC AGAGGAGTCCATCCCCAGGCAGGGGGAGACCC_GGGGGGTGAGCTTTAAGCAGGGCCTGGCAAGC CT C TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53227356..53227506 26863196 MeRIP-seq:(Medium) rs1166491710 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5393299,Human_RBP_ID_22480639 RMVar_hsa_circ_12957,RMVar_hsa_circ_48712,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_62840,RMVar_hsa_circ_31013,RMVar_hsa_circ_218880 87569 RMVar_ID_87569 Human_SNP_ID_133480620 m1A Human chr3 - 53228015 53228015 53228015 AAGGGGCCTCCAAAGTCATCAACTGAGCGGCCACTGCATGCTAGGTCTTGGGGTTCTTTCTTTCG AAGGGGCCTCCAAAGTCATCAACTGAGCGGCCGCTGCATGCTAGGTCTTGGGGTTCTTTCTTTCG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:53228013..53228393 26863196 MeRIP-seq:(Medium) rs782444805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21987581 RMVar_hsa_circ_12957,RMVar_hsa_circ_48712,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_62840,RMVar_hsa_circ_31013,RMVar_hsa_circ_218880 87570 RMVar_ID_87570 Human_SNP_ID_133480659 m1A Human chr3 + 53228105 53228105 53228105 GCAGCGGCCAAGGCCTCGTGCAGGGTCACCCCAGCCCCGATAACGGTCACCTGGTCATCCTTGCT GCAGCGGCCAAGGCCTCGTGCAGGGTCACCCCTGCCCCGATAACGGTCACCTGGTCATCCTTGCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:53228051..53228150;chr3:53228041..53228150 32194978 MeRIP-seq:(Medium) rs1382742901 Functional Loss SNV dbSNP153 33..33 33 - - - 87571 RMVar_ID_87571 Human_SNP_ID_133481109 m1A Human chr3 - 53229374 53229374 53229374 AACAGGACGGTGCCCTTCTGCAGCACTTTTGCAGCCTTCTTCACGCGGGCCTTTGACCAGATTCG AACAGGACGGTGCCCTTCTGCAGCACTTTTGCGGCCTTCTTCACGCGGGCCTTTGACCAGATTCG T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs201588631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68518,Human_RBP_ID_606048,Human_RBP_ID_8576479,Human_RBP_ID_9334211,Human_RBP_ID_17290705,Human_RBP_ID_17404657,Human_RBP_ID_17704412,Human_RBP_ID_18194629,Human_RBP_ID_18812143,Human_RBP_ID_22455485,Human_RBP_ID_26823953 Human_Splice_Rec_441186,Human_Splice_Rec_441187,Human_Splice_Rec_441212,Human_Splice_Rec_441213,Human_Splice_Rec_441228,Human_Splice_Rec_441229,Human_Splice_Rec_441238,Human_Splice_Rec_441239,Human_Splice_Rec_441264,Human_Splice_Rec_441265,Human_Splice_Rec_441292,Human_Splice_Rec_441293,Human_Splice_Rec_441316,Human_Splice_Rec_441317,Human_Splice_Rec_441342,Human_Splice_Rec_441343,Human_Splice_Rec_441351 RMVar_hsa_circ_12957,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_62840,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_17364,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_50432 87572 RMVar_ID_87572 Human_SNP_ID_133481470 m1A Human chr3 + 53230551 53230551 53230551 CCGAGAAGGTGGAATTTTTGGTGTCCCCATCCAGGGCGATGATGCGGTCACTGGCATGGCCCAGC CCGAGAAGGTGGAATTTTTGGTGTCCCCATCCGGGGCGATGATGCGGTCACTGGCATGGCCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53230502..53230574 26863196 MeRIP-seq:(Medium) rs781908334 Functional Loss SNV dbSNP153 33..33 33 - - - 87573 RMVar_ID_87573 Human_SNP_ID_133481479 m1A Human chr3 - 53230566 53230566 53230566 GCAGGCACTGGCCAAGCTGGGCCATGCCAGTGACCGCATCATCGCCCTGGATGGGGACACCAAAA GCAGGCACTGGCCAAGCTGGGCCATGCCAGTGGCCGCATCATCGCCCTGGATGGGGACACCAAAA T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1336717440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68520,Human_RBP_ID_247612,Human_RBP_ID_606054,Human_RBP_ID_1033892,Human_RBP_ID_17290707,Human_RBP_ID_18008565,Human_RBP_ID_18194632,Human_RBP_ID_22455978,Human_RBP_ID_26824799,Human_RBP_ID_27057464,Human_RBP_ID_27503999 Human_Splice_Rec_441184,Human_Splice_Rec_441210,Human_Splice_Rec_441226,Human_Splice_Rec_441236,Human_Splice_Rec_441262,Human_Splice_Rec_441290,Human_Splice_Rec_441314,Human_Splice_Rec_441340 RMVar_hsa_circ_9067,RMVar_hsa_circ_12957,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_62840,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_17364,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_50432,RMVar_hsa_circ_371400,RMVar_hsa_circ_34164,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885 87574 RMVar_ID_87574 Human_SNP_ID_133481798 m1A Human chr3 + 53231533 53231533 53231533 CATGTTTTTGGGGAGGGGCTTCCCATGCCAAGACTCCTTATCTTCTACCCCTGCAGACCCAACAC CATGTTTTTGGGGAGGGGCTTCCCATGCCAAGGCTCCTTATCTTCTACCCCTGCAGACCCAACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:53231409..53231576;chr3:53231427..53231598 26863196 MeRIP-seq:(Medium) rs922835613 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_27057488 87575 RMVar_ID_87575 Human_SNP_ID_133482245 m1A Human chr3 - 53233095 53233095 53233095 CTTCACCCCTCGCCCAGACACTGTGGCTACGTAGCTCTGACCCGCACATCCAGGGAAACAGCCCT CTTCACCCCTCGCCCAGACACTGTGGCTACGTGGCTCTGACCCGCACATCCAGGGAAACAGCCCT T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53233092..53233176 26863196 MeRIP-seq:(Medium) rs1468688889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115791,Human_RBP_ID_22363909 RMVar_hsa_circ_9067,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_17364,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_371400,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_301729 87576 RMVar_ID_87576 Human_SNP_ID_133482851 m1A Human chr3 - 53235030 53235030 53235030 ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCACTGCAGCACCAGATGGACATCTACCAGAAGCG ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCGCTGCAGCACCAGATGGACATCTACCAGAAGCG T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:53234890..53235077 26863196 MeRIP-seq:(Medium) rs1051485 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_68527,Human_RBP_ID_606074,Human_RBP_ID_783770,Human_RBP_ID_835695,Human_RBP_ID_7211418,Human_RBP_ID_9302935,Human_RBP_ID_18194643,Human_RBP_ID_22456734,Human_RBP_ID_22769319,Human_RBP_ID_22824733,Human_RBP_ID_26823956,Human_RBP_ID_27057530 Human_Splice_Rec_441179,Human_Splice_Rec_441205,Human_Splice_Rec_441256,Human_Splice_Rec_441257,Human_Splice_Rec_441285,Human_Splice_Rec_441309,Human_Splice_Rec_441335,Human_Splice_Rec_441365,Human_Splice_Rec_441371 GWAS_ID_10758,GWAS_ID_10759,GWAS_ID_10760,GWAS_ID_10761,GWAS_ID_10762,GWAS_ID_10763,GWAS_ID_10764,GWAS_ID_10765,GWAS_ID_10766,GWAS_ID_10767,GWAS_ID_10768,GWAS_ID_10769,GWAS_ID_10770,GWAS_ID_10771,GWAS_ID_10772,GWAS_ID_10773,GWAS_ID_10774,GWAS_ID_10775,GWAS_ID_10776,GWAS_ID_10777,GWAS_ID_10778,GWAS_ID_10779,GWAS_ID_10780,GWAS_ID_10781,GWAS_ID_10782,GWAS_ID_10783,GWAS_ID_10784,GWAS_ID_10785,GWAS_ID_10786,GWAS_ID_10787,GWAS_ID_10788,GWAS_ID_10789,GWAS_ID_10790,GWAS_ID_10791,GWAS_ID_10792,GWAS_ID_10793,GWAS_ID_10794,GWAS_ID_10795,GWAS_ID_10796,GWAS_ID_10797,GWAS_ID_10798,GWAS_ID_10799,GWAS_ID_10800,GWAS_ID_10801,GWAS_ID_10802,GWAS_ID_10803,GWAS_ID_10804,GWAS_ID_10805,GWAS_ID_10806,GWAS_ID_10807,GWAS_ID_10808,GWAS_ID_10809,GWAS_ID_10810,GWAS_ID_10811,GWAS_ID_10812,GWAS_ID_10813,GWAS_ID_10814,GWAS_ID_10815 RMVar_hsa_circ_9067,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_371400,RMVar_hsa_circ_218886,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_281638,RMVar_hsa_circ_31346 87577 RMVar_ID_87577 Human_SNP_ID_133482852 m1A Human chr3 - 53235030 53235030 53235030 ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCACTGCAGCACCAGATGGACATCTACCAGAAGCG ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCCCTGCAGCACCAGATGGACATCTACCAGAAGCG T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:53234890..53235077 26863196 MeRIP-seq:(Medium) rs1051485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68527,Human_RBP_ID_606074,Human_RBP_ID_783770,Human_RBP_ID_835695,Human_RBP_ID_7211418,Human_RBP_ID_9302935,Human_RBP_ID_18194643,Human_RBP_ID_22456734,Human_RBP_ID_22769319,Human_RBP_ID_22824733,Human_RBP_ID_26823956,Human_RBP_ID_27057530 Human_Splice_Rec_441179,Human_Splice_Rec_441205,Human_Splice_Rec_441256,Human_Splice_Rec_441257,Human_Splice_Rec_441285,Human_Splice_Rec_441309,Human_Splice_Rec_441335,Human_Splice_Rec_441365,Human_Splice_Rec_441371 GWAS_ID_10758,GWAS_ID_10759,GWAS_ID_10760,GWAS_ID_10761,GWAS_ID_10762,GWAS_ID_10763,GWAS_ID_10764,GWAS_ID_10765,GWAS_ID_10766,GWAS_ID_10767,GWAS_ID_10768,GWAS_ID_10769,GWAS_ID_10770,GWAS_ID_10771,GWAS_ID_10772,GWAS_ID_10773,GWAS_ID_10774,GWAS_ID_10775,GWAS_ID_10776,GWAS_ID_10777,GWAS_ID_10778,GWAS_ID_10779,GWAS_ID_10780,GWAS_ID_10781,GWAS_ID_10782,GWAS_ID_10783,GWAS_ID_10784,GWAS_ID_10785,GWAS_ID_10786,GWAS_ID_10787,GWAS_ID_10788,GWAS_ID_10789,GWAS_ID_10790,GWAS_ID_10791,GWAS_ID_10792,GWAS_ID_10793,GWAS_ID_10794,GWAS_ID_10795,GWAS_ID_10796,GWAS_ID_10797,GWAS_ID_10798,GWAS_ID_10799,GWAS_ID_10800,GWAS_ID_10801,GWAS_ID_10802,GWAS_ID_10803,GWAS_ID_10804,GWAS_ID_10805,GWAS_ID_10806,GWAS_ID_10807,GWAS_ID_10808,GWAS_ID_10809,GWAS_ID_10810,GWAS_ID_10811,GWAS_ID_10812,GWAS_ID_10813,GWAS_ID_10814,GWAS_ID_10815 RMVar_hsa_circ_9067,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_371400,RMVar_hsa_circ_218886,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_281638,RMVar_hsa_circ_31346 87578 RMVar_ID_87578 Human_SNP_ID_133482914 m1A Human chr3 + 53235183 53235182 53235184 CCCAGCAAGCAATAGACTCGGTAGCTGTGGACAGAGAGTGAATCAGGCCAGTCCCTCTCACCTGG CCCAGCAAGCAATAGACTCGGTAGCTGTGGAC__AGAGTGAATCAGGCCAGTCCCTCTCACCTGG CAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:53235176..53235200 26863196 MeRIP-seq:(Medium) rs782573644 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14899950 87579 RMVar_ID_87579 Human_SNP_ID_133483873 m1A Human chr3 - 53238637 53238637 53238637 CTAGAGGAGGAAGGCCAGTGGGGCCAGCCCGCAGGGTGTGAGAAGGGCCCAGTTCTGCAGCTGAT CTAGAGGAGGAAGGCCAGTGGGGCCAGCCCGCGGGGTGTGAGAAGGGCCCAGTTCTGCAGCTGAT T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:53238635..53238706 26863196 MeRIP-seq:(Medium) rs1319333669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9067,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_218885,RMVar_hsa_circ_31346 87580 RMVar_ID_87580 Human_SNP_ID_133484246 m1A Human chr3 + 53240215 53240215 53240215 AAGGGTGGGTCACCCAAGGACCACTCCCCAAAACTACCCAGGTTGGGGGTGGGGAGTAGGTGTGT AAGGGTGGGTCACCCAAGGACCACTCCCCAAATCTACCCAGGTTGGGGGTGGGGAGTAGGTGTGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:53240213..53240284 26863196 MeRIP-seq:(Medium) rs1553679470 Functional Loss SNV dbSNP153 33..33 33 - - - 87581 RMVar_ID_87581 Human_SNP_ID_133484834 m1A Human chr3 - 53242208 53242208 53242208 ACCCCACGTCATGCTGCAGCGCCGCAGAGATCATGGCTGTCCTCTTTTTCCACACCATGCGCTAC ACCCCACGTCATGCTGCAGCGCCGCAGAGATCGTGGCTGTCCTCTTTTTCCACACCATGCGCTAC T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:53242126..53242279;chr3:53242069..53242304 26863196 MeRIP-seq:(Medium) rs782320926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68537,Human_RBP_ID_1033903,Human_RBP_ID_7211453,Human_RBP_ID_14900115,Human_RBP_ID_18194652,Human_RBP_ID_18209923,Human_RBP_ID_26824806,Human_RBP_ID_27504028 Human_Splice_Rec_441172,Human_Splice_Rec_441173,Human_Splice_Rec_441198,Human_Splice_Rec_441199,Human_Splice_Rec_441250,Human_Splice_Rec_441251,Human_Splice_Rec_441276,Human_Splice_Rec_441277,Human_Splice_Rec_441304,Human_Splice_Rec_441305,Human_Splice_Rec_441328,Human_Splice_Rec_441329,Human_Splice_Rec_441356,Human_Splice_Rec_441357,Human_Splice_Rec_441373,Human_Splice_Rec_441380 RMVar_hsa_circ_9067,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_48083,RMVar_hsa_circ_286595,RMVar_hsa_circ_31346,RMVar_hsa_circ_286431,RMVar_hsa_circ_218888,RMVar_hsa_circ_218887,RMVar_hsa_circ_357432,RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 87582 RMVar_ID_87582 Human_SNP_ID_133484848 m1A Human chr3 - 53242240 53242240 53242240 CCTGTGTCTGTCTTCTCTCCTGGGCCACAGCCACCCCACGTCATGCTGCAGCGCCGCAGAGATCA CCTGTGTCTGTCTTCTCTCCTGGGCCACAGCCCCCCCACGTCATGCTGCAGCGCCGCAGAGATCA T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr3:53242077..53242294;chr3:53242151..53242306 26863196,26863410 MeRIP-seq:(Medium) rs1553680078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68537,Human_RBP_ID_247624,Human_RBP_ID_937263,Human_RBP_ID_18194652,Human_RBP_ID_22456740,Human_RBP_ID_25746321,Human_RBP_ID_26823960 Human_Splice_Rec_441172,Human_Splice_Rec_441198,Human_Splice_Rec_441250,Human_Splice_Rec_441276,Human_Splice_Rec_441304,Human_Splice_Rec_441328,Human_Splice_Rec_441356,Human_Splice_Rec_441380 Human_miRNA_ID_1936412,Human_miRNA_ID_1947512 RMVar_hsa_circ_9067,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_48083,RMVar_hsa_circ_286595,RMVar_hsa_circ_31346,RMVar_hsa_circ_286431,RMVar_hsa_circ_218888,RMVar_hsa_circ_218887,RMVar_hsa_circ_357432,RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 87583 RMVar_ID_87583 Human_SNP_ID_133484850 m1A Human chr3 - 53242244 53242244 53242244 GATGCCTGTGTCTGTCTTCTCTCCTGGGCCACAGCCACCCCACGTCATGCTGCAGCGCCGCAGAG GATGCCTGTGTCTGTCTTCTCTCCTGGGCCACTGCCACCCCACGTCATGCTGCAGCGCCGCAGAG T A TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:53242226..53242250;chr3:53242199..53256002;chr3:53242199..53256025 26863196,32194978,32194978 MeRIP-seq:(Medium) rs113747453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68537,Human_RBP_ID_937263,Human_RBP_ID_25746321 RMVar_hsa_circ_48083,RMVar_hsa_circ_286431,RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 87584 RMVar_ID_87584 Human_SNP_ID_133484851 m1A Human chr3 - 53242244 53242244 53242244 GATGCCTGTGTCTGTCTTCTCTCCTGGGCCACAGCCACCCCACGTCATGCTGCAGCGCCGCAGAG GATGCCTGTGTCTGTCTTCTCTCCTGGGCCACGGCCACCCCACGTCATGCTGCAGCGCCGCAGAG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:53242226..53242250;chr3:53242199..53256002;chr3:53242199..53256025 26863196,32194978,32194978 MeRIP-seq:(Medium) rs113747453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68537,Human_RBP_ID_937263,Human_RBP_ID_25746321 RMVar_hsa_circ_48083,RMVar_hsa_circ_286431,RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 87585 RMVar_ID_87585 Human_SNP_ID_133488320 m1A Human chr3 - 53255884 53255884 53255884 GCAGAAGCTGCAGGCCTTGAAGGACACGGCCAACCGCCTACGTATCAGCTCCATCCAGGCCACCA GCAGAAGCTGCAGGCCTTGAAGGACACGGCCAGCCGCCTACGTATCAGCTCCATCCAGGCCACCA T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:53255743..53256025 26863196 MeRIP-seq:(Medium) rs782595403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606086,Human_RBP_ID_1629912,Human_RBP_ID_1966027,Human_RBP_ID_4767015,Human_RBP_ID_8576527,Human_RBP_ID_18194654,Human_RBP_ID_18812169,Human_RBP_ID_20786916,Human_RBP_ID_22456741,Human_RBP_ID_26823964 Human_Splice_Rec_441171,Human_Splice_Rec_441197,Human_Splice_Rec_441249,Human_Splice_Rec_441275,Human_Splice_Rec_441303,Human_Splice_Rec_441327,Human_Splice_Rec_441353,Human_Splice_Rec_441379 RMVar_hsa_circ_91143,RMVar_hsa_circ_107537,RMVar_hsa_circ_218889,RMVar_hsa_circ_218890 87586 RMVar_ID_87586 Human_SNP_ID_133488321 m1A Human chr3 - 53255885 53255885 53255885 AGCAGAAGCTGCAGGCCTTGAAGGACACGGCCAACCGCCTACGTATCAGCTCCATCCAGGCCACC AGCAGAAGCTGCAGGCCTTGAAGGACACGGCCCACCGCCTACGTATCAGCTCCATCCAGGCCACC T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:53255749..53256025 26863196 MeRIP-seq:(Medium) rs1366477714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68539,Human_RBP_ID_606086,Human_RBP_ID_1629913,Human_RBP_ID_1966027,Human_RBP_ID_4767015,Human_RBP_ID_8576527,Human_RBP_ID_18194654,Human_RBP_ID_22456741,Human_RBP_ID_26823964 Human_Splice_Rec_441171,Human_Splice_Rec_441197,Human_Splice_Rec_441249,Human_Splice_Rec_441275,Human_Splice_Rec_441303,Human_Splice_Rec_441327,Human_Splice_Rec_441353,Human_Splice_Rec_441379 RMVar_hsa_circ_91143,RMVar_hsa_circ_107537,RMVar_hsa_circ_218889,RMVar_hsa_circ_218890 87587 RMVar_ID_87587 Human_SNP_ID_133488326 m1A Human chr3 - 53255893 53255893 53255893 GCCTGACCAGCAGAAGCTGCAGGCCTTGAAGGACACGGCCAACCGCCTACGTATCAGCTCCATCC GCCTGACCAGCAGAAGCTGCAGGCCTTGAAGGCCACGGCCAACCGCCTACGTATCAGCTCCATCC T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:53255763..53256025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_68539,Human_RBP_ID_606086,Human_RBP_ID_1629913,Human_RBP_ID_1966027,Human_RBP_ID_4758837,Human_RBP_ID_8576527,Human_RBP_ID_18194654,Human_RBP_ID_22456741,Human_RBP_ID_26823964 Human_Splice_Rec_441171,Human_Splice_Rec_441197,Human_Splice_Rec_441249,Human_Splice_Rec_441275,Human_Splice_Rec_441303,Human_Splice_Rec_441327,Human_Splice_Rec_441353,Human_Splice_Rec_441379 RMVar_hsa_circ_91143,RMVar_hsa_circ_107537,RMVar_hsa_circ_218889,RMVar_hsa_circ_218890 87588 RMVar_ID_87588 Human_SNP_ID_133497452 m1A Human chr3 - 53292491 53292491 53292491 ACACAATCCCGTTGAGCCCTGTTCTCAGTCCCACTCTGCCAGCTGAAGCTCCTACTGCACAGGTT ACACAATCCCGTTGAGCCCTGTTCTCAGTCCCGCTCTGCCAGCTGAAGCTCCTACTGCACAGGTT T C DCP1A Ensembl:ENSG00000272886 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:53292442..53292554 26863196 MeRIP-seq:(Medium) rs782157688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606187,Human_RBP_ID_7211592,Human_RBP_ID_14900790,Human_RBP_ID_17290720,Human_RBP_ID_17404659 RMVar_hsa_circ_14455,RMVar_hsa_circ_320801,RMVar_hsa_circ_329185,RMVar_hsa_circ_23094,RMVar_hsa_circ_274359,RMVar_hsa_circ_376412,RMVar_hsa_circ_27487 87589 RMVar_ID_87589 Human_SNP_ID_133511324 m1A Human chr3 - 53347484 53347484 53347484 TGGAGGCGCTGAGTCGAGCTGGGCAGGAGATGAGCCTAGCGGCCCTGAAGCAACACGACCCCTAT TGGAGGCGCTGAGTCGAGCTGGGCAGGAGATGGGCCTAGCGGCCCTGAAGCAACACGACCCCTAT T C DCP1A Ensembl:ENSG00000272886 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:53347376..53347550;chr3:53347404..53347517 26863196 MeRIP-seq:(Medium) rs1449088491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248718,Human_RBP_ID_9395209,Human_RBP_ID_14901695,Human_RBP_ID_18008639 Human_Splice_Rec_441417 87590 RMVar_ID_87590 Human_SNP_ID_133511333 m1A Human chr3 - 53347492 53347492 53347492 ATTCAAGATGGAGGCGCTGAGTCGAGCTGGGCAGGAGATGAGCCTAGCGGCCCTGAAGCAACACG ATTCAAGATGGAGGCGCTGAGTCGAGCTGGGCTGGAGATGAGCCTAGCGGCCCTGAAGCAACACG T A DCP1A Ensembl:ENSG00000272886 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:53347424..53347509;chr3:53347391..53347508 26863196 MeRIP-seq:(Medium) rs1553693313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248718,Human_RBP_ID_7211757,Human_RBP_ID_9395209,Human_RBP_ID_14901696,Human_RBP_ID_18008639 Human_Splice_Rec_441417 87591 RMVar_ID_87591 Human_SNP_ID_133632559 m1A Human chr3 - 53846309 53846309 53846309 CCGCGCACACGTGCATGCAGTGAGCCAGGTGCATCAGCTGCACCCGCCCTCGGGCTTCGCGCGCC CCGCGCACACGTGCATGCAGTGAGCCAGGTGCGTCAGCTGCACCCGCCCTCGGGCTTCGCGCGCC T C CHDH Ensembl:ENSG00000016391 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53846260..53846385 26863196 MeRIP-seq:(Medium) rs1435124948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756559 RMVar_hsa_circ_116792,RMVar_hsa_circ_218917,RMVar_hsa_circ_86957,RMVar_hsa_circ_218918 87592 RMVar_ID_87592 Human_SNP_ID_133637693 m1A Human chr3 - 53866228 53866228 53866228 AGGCTTACACCATCACACTCAGCTAATTTTTTAAATCTTTTGTAGAGATGGAGGTCTCGCTTTGT AGGCTTACACCATCACACTCAGCTAATTTTTTTAATCTTTTGTAGAGATGGAGGTCTCGCTTTGT T A - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1156433023 Functional Loss SNV dbSNP153 33..33 33 - - - 87593 RMVar_ID_87593 Human_SNP_ID_133641300 m1A Human chr3 - 53880107 53880107 53880107 AAGTCACACATCTATGTTTTATATCTGCAGCAAATCCAGAGCAACTTCATCATTGTCATACATCC AAGTCACACATCTATGTTTTATATCTGCAGCAGATCCAGAGCAACTTCATCATTGTCATACATCC T C ACTR8 Ensembl:ENSG00000113812 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:53879979..53881734;chr3:53878458..53881784 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3712481 Human_Splice_Rec_442592,Human_Splice_Rec_442660 RMVar_hsa_circ_54334,RMVar_hsa_circ_218931,RMVar_hsa_circ_316890 87594 RMVar_ID_87594 Human_SNP_ID_133641831 m1A Human chr3 - 53882094 53882094 53882094 AGGTTGGTGGGTGTCTCCGGCCATAATGACCCAGGCTGAGAAGGGTGATACGGAGAACGGAAAGG AGGTTGGTGGGTGTCTCCGGCCATAATGACCCCGGCTGAGAAGGGTGATACGGAGAACGGAAAGG T G ACTR8 Ensembl:ENSG00000113812 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:53881939..53882150;chr3:53881914..53882150 26863196 MeRIP-seq:(Medium) rs1186550752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4750757,Human_RBP_ID_18812249 87595 RMVar_ID_87595 Human_SNP_ID_133641839 m1A Human chr3 + 53882103 53882103 53882103 TCTCCGTATCACCCTTCTCAGCCTGGGTCATTATGGCCGGAGACACCCACCAACCTCTCGCCTCA TCTCCGTATCACCCTTCTCAGCCTGGGTCATTCTGGCCGGAGACACCCACCAACCTCTCGCCTCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:53881993..53882152 26863196 MeRIP-seq:(Medium) rs2276845 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10816,GWAS_ID_10817,GWAS_ID_10818,GWAS_ID_10819,GWAS_ID_10820,GWAS_ID_10821,GWAS_ID_10822,GWAS_ID_10823,GWAS_ID_10824,GWAS_ID_10825,GWAS_ID_10826,GWAS_ID_10827,GWAS_ID_10828,GWAS_ID_10829,GWAS_ID_10830,GWAS_ID_10831,GWAS_ID_10832,GWAS_ID_10833,GWAS_ID_10834,GWAS_ID_10835,GWAS_ID_10836,GWAS_ID_10837,GWAS_ID_10838,GWAS_ID_10839,GWAS_ID_10840 87596 RMVar_ID_87596 Human_SNP_ID_133641840 m1A Human chr3 + 53882103 53882103 53882103 TCTCCGTATCACCCTTCTCAGCCTGGGTCATTATGGCCGGAGACACCCACCAACCTCTCGCCTCA TCTCCGTATCACCCTTCTCAGCCTGGGTCATTGTGGCCGGAGACACCCACCAACCTCTCGCCTCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:53881993..53882152 26863196 MeRIP-seq:(Medium) rs2276845 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - GWAS_ID_10816,GWAS_ID_10817,GWAS_ID_10818,GWAS_ID_10819,GWAS_ID_10820,GWAS_ID_10821,GWAS_ID_10822,GWAS_ID_10823,GWAS_ID_10824,GWAS_ID_10825,GWAS_ID_10826,GWAS_ID_10827,GWAS_ID_10828,GWAS_ID_10829,GWAS_ID_10830,GWAS_ID_10831,GWAS_ID_10832,GWAS_ID_10833,GWAS_ID_10834,GWAS_ID_10835,GWAS_ID_10836,GWAS_ID_10837,GWAS_ID_10838,GWAS_ID_10839,GWAS_ID_10840 87597 RMVar_ID_87597 Human_SNP_ID_133643393 m1A Human chr3 - 53888482 53888482 53888482 TCACTAAAGTTTCTTTAATTCTTATCTGTAGGACAAGTGTTGGACAGCCGGAGTCAGTCTCCATG TCACTAAAGTTTCTTTAATTCTTATCTGTAGGGCAAGTGTTGGACAGCCGGAGTCAGTCTCCATG T C SELENOK Ensembl:ENSG00000113811 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr3:53888443..53890984;chr3:53888393..53890984;chr3:53888393..53890935 26863196,32194978 MeRIP-seq:(Medium) rs1409716676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933230,Human_RBP_ID_4757324,Human_RBP_ID_8576612,Human_RBP_ID_14902205,Human_RBP_ID_22457375,Human_RBP_ID_26348192,Human_RBP_ID_26824812 Human_Splice_Rec_442668,Human_Splice_Rec_442669,Human_Splice_Rec_442676,Human_Splice_Rec_442677,Human_Splice_Rec_442684,Human_Splice_Rec_442685,Human_Splice_Rec_442692,Human_Splice_Rec_442696 RMVar_hsa_circ_313913 87598 RMVar_ID_87598 Human_SNP_ID_133699584 m1A Human chr3 - 54122673 54122671 54122673 CCCTCCGACGCGCCCGCTGCGGCGGCGACGAGAGCGGCCGCGGGGAGCTGCGCGGAGCGGGCGGT CCCTCCGACGCGCCCGCTGCGGCGGCGACGAG__CGGCCGCGGGGAGCTGCGCGGAGCGGGCGGT GCT G AC115282.1 Ensembl:ENSG00000286353 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:54122586..54122682 26863410 MeRIP-seq:(Medium) rs1055255977 Functional Loss DEL dbSNP153 33..34 33 - - - 87599 RMVar_ID_87599 Human_SNP_ID_133699586 m1A Human chr3 - 54122673 54122673 54122673 CCCTCCGACGCGCCCGCTGCGGCGGCGACGAGAGCGGCCGCGGGGAGCTGCGCGGAGCGGGCGGT CCCTCCGACGCGCCCGCTGCGGCGGCGACGAGGGCGGCCGCGGGGAGCTGCGCGGAGCGGGCGGT T C AC115282.1 Ensembl:ENSG00000286353 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:54122586..54122682 26863410 MeRIP-seq:(Medium) rs747389577 Functional Loss SNV dbSNP153 33..33 33 - - - 87600 RMVar_ID_87600 Human_SNP_ID_133699597 m1A Human chr3 + 54122688 54122688 54122688 CAGCTCCCCGCGGCCGCTCTCGTCGCCGCCGCAGCGGGCGCGTCGGAGGGAGCCCAGCATGGCCG CAGCTCCCCGCGGCCGCTCTCGTCGCCGCCGCGGCGGGCGCGTCGGAGGGAGCCCAGCATGGCCG A G CACNA2D3 Ensembl:ENSG00000157445 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:54122638..54122776;chr3:54122650..54122752 26863196 MeRIP-seq:(Medium) rs1005102331 Functional Loss SNV dbSNP153 33..33 33 - - - 87601 RMVar_ID_87601 Human_SNP_ID_133707023 m1A Human chr3 - 54150788 54150786 54150788 GTATTAAGCACCAATTCCACAGCTACACCAAGAGTTATCTCCTCTTAGAATACATCCTAATCCTC GTATTAAGCACCAATTCCACAGCTACACCAAG__TTATCTCCTCTTAGAATACATCCTAATCCTC ACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:54150778..54151402 26863196 MeRIP-seq:(Medium) rs1332949315 Functional Loss DEL dbSNP153 33..34 33 - - - 87602 RMVar_ID_87602 Human_SNP_ID_133723628 m1A Human chr3 + 54217900 54217900 54217900 GAGACAGAGAGAGAGAGAGACAGGTGTTAGGGAGAGAGGTGTGTTAGAGAGAAAGAGATGTGTTA GAGACAGAGAGAGAGAGAGACAGGTGTTAGGGGGAGAGGTGTGTTAGAGAGAAAGAGATGTGTTA A G CACNA2D3 Ensembl:ENSG00000157445 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:54217896..54218075 26863196 MeRIP-seq:(Medium) rs1363064361 Functional Loss SNV dbSNP153 33..33 33 - - - 87603 RMVar_ID_87603 Human_SNP_ID_134056244 m1A Human chr3 - 55467147 55467147 55467147 ACTGCAACTATTGCACCTCTCTATTTGAATTTACTGTGGACCATGTGTGGTGTCTCTATGCCCTT ACTGCAACTATTGCACCTCTCTATTTGAATTTGCTGTGGACCATGTGTGGTGTCTCTATGCCCTT T C WNT5A Ensembl:ENSG00000114251 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1829556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606309 Human_miRNA_ID_1081417,Human_miRNA_ID_2884291 Clinvar_Rec_483 GWAS_ID_10841,GWAS_ID_10842,GWAS_ID_10843,GWAS_ID_10844 RMVar_hsa_circ_218958,RMVar_hsa_circ_97111,RMVar_hsa_circ_99638,RMVar_hsa_circ_76776,RMVar_hsa_circ_218959,RMVar_hsa_circ_218957 87604 RMVar_ID_87604 Human_SNP_ID_134059917 m1A Human chr3 - 55481303 55481303 55481303 CCCAGGTTGGGGAGAGGACGGAGGGTGGCCGCAGCGGGTTCCTGAGTGAATTACCCAGGAGGGAC CCCAGGTTGGGGAGAGGACGGAGGGTGGCCGCGGCGGGTTCCTGAGTGAATTACCCAGGAGGGAC T C WNT5A Ensembl:ENSG00000114251 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:55481151..55481350 26863196 MeRIP-seq:(Medium) rs1323361544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218961,RMVar_hsa_circ_99638,RMVar_hsa_circ_218959,RMVar_hsa_circ_107912 87605 RMVar_ID_87605 Human_SNP_ID_134061636 m1A Human chr3 + 55487086 55487086 55487086 GCGACCGGGTTAAGCCTGGGGGGACGGTCAGGAGCAGGGCTGCGGAGTCCTCCGGCGCGCGTCCG GCGACCGGGTTAAGCCTGGGGGGACGGTCAGGGGCAGGGCTGCGGAGTCCTCCGGCGCGCGTCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr3:55487002..55487344;chr3:55487001..55487265;chr3:55487035..55487136 26863196 MeRIP-seq:(Medium) rs1351844292 Functional Loss SNV dbSNP153 33..33 33 - - - 87606 RMVar_ID_87606 Human_SNP_ID_134061988 m1A Human chr3 + 55488156 55488156 55488156 GGGTCCGAGGGGCGGGAGAGCGGGCCGGCGGGAGGCGGGCGGTCCCGGGCACAACGGCGGCGGCG GGGTCCGAGGGGCGGGAGAGCGGGCCGGCGGGGGGCGGGCGGTCCCGGGCACAACGGCGGCGGCG A G WNT5A-AS1 Ensembl:ENSG00000244586 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:55488019..55488274 26863196 MeRIP-seq:(Medium) rs1416255779 Functional Loss SNV dbSNP153 33..33 33 - - - 87607 RMVar_ID_87607 Human_SNP_ID_134062521 m1A Human chr3 - 55489776 55489773 55489776 ACTGTAAAATGCCCACAGGTCGGGAAGTGGTCAAGGTTTACAGAGGAGAAGGTTAGAGGAATGGA ACTGTAAAATGCCCACAGGTCGGGAAGTGGTC___GTTTACAGAGGAGAAGGTTAGAGGAATGGA CCTT C WNT5A Ensembl:ENSG00000114251 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:55489725..55489909 26863196 MeRIP-seq:(Medium) rs1270665230 Functional Loss DEL dbSNP153 33..35 33 - - - 87608 RMVar_ID_87608 Human_SNP_ID_134334578 m1A Human chr3 + 56613656 56613653 56613657 GAAGAAACAACTGGAGGAAGAGCAAAGAAAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTAGCAC GAAGAAACAACTGGAGGAAGAGCAAAGAAA____GAAGAACAAGAAGAGGAGCTTCGCTTAGCAC AGAAG A CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:56613607..56613709 26863196 MeRIP-seq:(Medium) rs1340499694 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_247921,Human_RBP_ID_935518,Human_RBP_ID_22284759,Human_RBP_ID_24547275,Human_RBP_ID_26348196 Human_Splice_Rec_443532,Human_Splice_Rec_443533,Human_Splice_Rec_443574,Human_Splice_Rec_443575,Human_Splice_Rec_443608,Human_Splice_Rec_443609,Human_Splice_Rec_443674,Human_Splice_Rec_443675,Human_Splice_Rec_443718,Human_Splice_Rec_443719,Human_Splice_Rec_443760,Human_Splice_Rec_443761,Human_Splice_Rec_443786,Human_Splice_Rec_443787 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_353235,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_59971,RMVar_hsa_circ_367613 87609 RMVar_ID_87609 Human_SNP_ID_134334579 m1A Human chr3 + 56613656 56613656 56613656 GAAGAAACAACTGGAGGAAGAGCAAAGAAAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTAGCAC GAAGAAACAACTGGAGGAAGAGCAAAGAAAGATGGAAGAACAAGAAGAGGAGCTTCGCTTAGCAC A T CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:56613607..56613709 26863196 MeRIP-seq:(Medium) rs776571183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247921,Human_RBP_ID_935518,Human_RBP_ID_22284759,Human_RBP_ID_24547275,Human_RBP_ID_26348196 Human_Splice_Rec_443532,Human_Splice_Rec_443533,Human_Splice_Rec_443574,Human_Splice_Rec_443575,Human_Splice_Rec_443608,Human_Splice_Rec_443609,Human_Splice_Rec_443674,Human_Splice_Rec_443675,Human_Splice_Rec_443718,Human_Splice_Rec_443719,Human_Splice_Rec_443760,Human_Splice_Rec_443761,Human_Splice_Rec_443786,Human_Splice_Rec_443787 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_353235,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_59971,RMVar_hsa_circ_367613 87610 RMVar_ID_87610 Human_SNP_ID_134334583 m1A Human chr3 + 56613666 56613664 56613667 CTGGAGGAAGAGCAAAGAAAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTAGCACAGGAACGTGA CTGGAGGAAGAGCAAAGAAAGAAGGAAGAAC___AAGAGGAGCTTCGCTTAGCACAGGAACGTGA CAAG C CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:56613616..56613711 26863196 MeRIP-seq:(Medium) rs767806017 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_247921,Human_RBP_ID_935518,Human_RBP_ID_22284759,Human_RBP_ID_24547275,Human_RBP_ID_26348196 Human_Splice_Rec_443532,Human_Splice_Rec_443533,Human_Splice_Rec_443574,Human_Splice_Rec_443575,Human_Splice_Rec_443608,Human_Splice_Rec_443609,Human_Splice_Rec_443674,Human_Splice_Rec_443675,Human_Splice_Rec_443718,Human_Splice_Rec_443719,Human_Splice_Rec_443760,Human_Splice_Rec_443761,Human_Splice_Rec_443786,Human_Splice_Rec_443787 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_353235,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_59971,RMVar_hsa_circ_367613 87611 RMVar_ID_87611 Human_SNP_ID_134334961 m1A Human chr3 + 56615171 56615171 56615171 TCTCAAGACAAATGAGCTATTCCAGACAATGCAGCGAGCACAGGAACTGGCACAGAGACTAAAAC TCTCAAGACAAATGAGCTATTCCAGACAATGCGGCGAGCACAGGAACTGGCACAGAGACTAAAAC A G CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:56615079..56615171 26863196 MeRIP-seq:(Medium) rs1441855123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69285,Human_RBP_ID_14904969 Human_Splice_Rec_443534,Human_Splice_Rec_443576,Human_Splice_Rec_443610,Human_Splice_Rec_443676,Human_Splice_Rec_443720,Human_Splice_Rec_443762,Human_Splice_Rec_443788 Human_miRNA_ID_980889,Human_miRNA_ID_985614,Human_miRNA_ID_2445002,Human_miRNA_ID_2446388 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_367613,RMVar_hsa_circ_52166 87612 RMVar_ID_87612 Human_SNP_ID_134353853 m1A Human chr3 + 56682722 56682722 56682722 CTCTTCCTGGGGATCTGAAAACTCCTCCTAACAGGCCTTTCGGGCTCTTCGGGGCCTCTGGGCAG CTCTTCCTGGGGATCTGAAAACTCCTCCTAACGGGCCTTTCGGGCTCTTCGGGGCCTCTGGGCAG A G HSALNG0026336 RNACentral:URS0000E97708 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:56682701..56682725 26863196 MeRIP-seq:(Medium) rs1305551096 Functional Loss SNV dbSNP153 33..33 33 - - - 87613 RMVar_ID_87613 Human_SNP_ID_134353984 m1A Human chr3 - 56682933 56682933 56682933 TGCGAGTTGGGAAAGTGGCGGCGGCGGAGACGACGAGATGAAGCAGGCGCTTCCGGAGCTTGAGT TGCGAGTTGGGAAAGTGGCGGCGGCGGAGACGGCGAGATGAAGCAGGCGCTTCCGGAGCTTGAGT T C TASOR Ensembl:ENSG00000163946 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:56682801..56683250 26863196 MeRIP-seq:(Medium) rs1052259496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247646,Human_RBP_ID_606466,Human_RBP_ID_937151,Human_RBP_ID_4757326,Human_RBP_ID_8875058,Human_RBP_ID_9302941,Human_RBP_ID_9395237,Human_RBP_ID_23026635,Human_RBP_ID_23119928,Human_RBP_ID_25748259,Human_RBP_ID_26348198 RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 87614 RMVar_ID_87614 Human_SNP_ID_134353996 m1A Human chr3 + 56682959 56682959 56682959 ATCTCGTCGTCTCCGCCGCCGCCACTTTCCCAACTCGCATCCGTCGGCTGACAGGCCTCCGTCTC ATCTCGTCGTCTCCGCCGCCGCCACTTTCCCAGCTCGCATCCGTCGGCTGACAGGCCTCCGTCTC A G HSALNG0026336 RNACentral:URS0000E97708 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:56682826..56683025 26863196 MeRIP-seq:(Medium) rs1201637478 Functional Loss SNV dbSNP153 33..33 33 - - - 87615 RMVar_ID_87615 Human_SNP_ID_134354063 m1A Human chr3 - 56683100 56683100 56683100 GGCCACGGGGGGAAGGGGGTGGGTGGGCTGAGAGCAGCTCGGCGGCGAGACTGGCCCGCCGCCCC GGCCACGGGGGGAAGGGGGTGGGTGGGCTGAGGGCAGCTCGGCGGCGAGACTGGCCCGCCGCCCC T C TASOR Ensembl:ENSG00000163946 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:56683051..56683100 26863196 MeRIP-seq:(Medium) rs1015745761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937152,Human_RBP_ID_4757327,Human_RBP_ID_8875059,Human_RBP_ID_9302359,Human_RBP_ID_9395237,Human_RBP_ID_22093082,Human_RBP_ID_22725768 RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 87616 RMVar_ID_87616 Human_SNP_ID_134354069 m1A Human chr3 + 56683113 56683113 56683113 AGTCTCGCCGCCGAGCTGCTCTCAGCCCACCCACCCCCTTCCCCCCGTGGCCTCAGGCTGCGCTC AGTCTCGCCGCCGAGCTGCTCTCAGCCCACCCCCCCCCTTCCCCCCGTGGCCTCAGGCTGCGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:56683062..56683233 26863196 MeRIP-seq:(Medium) rs1445620107 Functional Loss SNV dbSNP153 33..33 33 - - - 87617 RMVar_ID_87617 Human_SNP_ID_134354072 m1A Human chr3 - 56683119 56683119 56683119 GGTCGGGAGCGCAGCCTGAGGCCACGGGGGGAAGGGGGTGGGTGGGCTGAGAGCAGCTCGGCGGC GGTCGGGAGCGCAGCCTGAGGCCACGGGGGGAGGGGGGTGGGTGGGCTGAGAGCAGCTCGGCGGC T C TASOR Ensembl:ENSG00000163946 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:56683069..56683227 26863196 MeRIP-seq:(Medium) rs1292714275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758141,Human_RBP_ID_5506715,Human_RBP_ID_9302359,Human_RBP_ID_9395237,Human_RBP_ID_22725768,Human_RBP_ID_27504189 87618 RMVar_ID_87618 Human_SNP_ID_134384166 m1A Human chr3 - 56801814 56801814 56801814 CGCCTAGGGTCAGCGGTGACATCCCAAAGGGCAGGCCCGGCAGCCGCCATGGTGGCCAAGGATTA CGCCTAGGGTCAGCGGTGACATCCCAAAGGGCGGGCCCGGCAGCCGCCATGGTGGCCAAGGATTA T C ARHGEF3 Ensembl:ENSG00000163947 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:56801767..56801899 26863196 MeRIP-seq:(Medium) rs1242357158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9395238 RMVar_hsa_circ_17525,RMVar_hsa_circ_308921 87619 RMVar_ID_87619 Human_SNP_ID_134487282 m1A Human chr3 - 57227806 57227806 57227806 AGCTCCCCGCGCCGGCCCGCCCGCCGCAGCTGACCCCGGCCCGCCCTCTCCGGCAAGGGCTGCAG AGCTCCCCGCGCCGGCCCGCCCGCCGCAGCTGGCCCCGGCCCGCCCTCTCCGGCAAGGGCTGCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:57227770..57227950 26863196 MeRIP-seq:(Medium) rs1216674649 Functional Loss SNV dbSNP153 33..33 33 - - - 87620 RMVar_ID_87620 Human_SNP_ID_134487297 m1A Human chr3 + 57227835 57227835 57227835 GGGTCAGCTGCGGCGGGCGGGCCGGCGCGGGGAGCTGTGGGCGGCAGCTGCGTCTCCTGCCACCG GGGTCAGCTGCGGCGGGCGGGCCGGCGCGGGGCGCTGTGGGCGGCAGCTGCGTCTCCTGCCACCG A C APPL1 Ensembl:ENSG00000157500 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:57227786..57230762 26863196 MeRIP-seq:(Medium) rs769044973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248365,Human_RBP_ID_4756564,Human_RBP_ID_18424244 87621 RMVar_ID_87621 Human_SNP_ID_134487298 m1A Human chr3 + 57227835 57227835 57227835 GGGTCAGCTGCGGCGGGCGGGCCGGCGCGGGGAGCTGTGGGCGGCAGCTGCGTCTCCTGCCACCG GGGTCAGCTGCGGCGGGCGGGCCGGCGCGGGGGGCTGTGGGCGGCAGCTGCGTCTCCTGCCACCG A G APPL1 Ensembl:ENSG00000157500 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:57227786..57230762 26863196 MeRIP-seq:(Medium) rs769044973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248365,Human_RBP_ID_4756564,Human_RBP_ID_18424244 87622 RMVar_ID_87622 Human_SNP_ID_134571192 m1A Human chr3 + 57556598 57556597 57556598 ATGCAGCGCGACCAGAGCGAGCCGCTGGGTCGAGTCCTCAGCCGCATCGCTACCAATGCCCTAAA ATGCAGCGCGACCAGAGCGAGCCGCTGGGTCG_GTCCTCAGCCGCATCGCTACCAATGCCCTAAA GA G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs749859072 Functional Loss DEL dbSNP153 33..33 33 - - - 87623 RMVar_ID_87623 Human_SNP_ID_134581232 m1A Human chr3 - 57597181 57597181 57597181 AGCTTGAAAGGAGAAAGCACGGGGTCGCCCCAAACCCCTTCTGCTTCTGCCCATCACAAGTGCCA AGCTTGAAAGGAGAAAGCACGGGGTCGCCCCAGACCCCTTCTGCTTCTGCCCATCACAAGTGCCA T C ARF4 Ensembl:ENSG00000168374 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:57597131..57597400 26863196 MeRIP-seq:(Medium) rs750788612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68779,Human_RBP_ID_936567,Human_RBP_ID_4751396,Human_RBP_ID_5425592,Human_RBP_ID_5447806,Human_RBP_ID_5506723,Human_RBP_ID_5530951,Human_RBP_ID_8577134,Human_RBP_ID_27321634 Human_Splice_Rec_445016,Human_Splice_Rec_445032 Human_miRNA_ID_2383899 RMVar_hsa_circ_76920,RMVar_hsa_circ_219107,RMVar_hsa_circ_219108 87624 RMVar_ID_87624 Human_SNP_ID_134581233 m1A Human chr3 - 57597181 57597181 57597181 AGCTTGAAAGGAGAAAGCACGGGGTCGCCCCAAACCCCTTCTGCTTCTGCCCATCACAAGTGCCA AGCTTGAAAGGAGAAAGCACGGGGTCGCCCCACACCCCTTCTGCTTCTGCCCATCACAAGTGCCA T G ARF4 Ensembl:ENSG00000168374 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:57597131..57597400 26863196 MeRIP-seq:(Medium) rs750788612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68779,Human_RBP_ID_936567,Human_RBP_ID_4751396,Human_RBP_ID_5425592,Human_RBP_ID_5447806,Human_RBP_ID_5506723,Human_RBP_ID_5530951,Human_RBP_ID_8577134,Human_RBP_ID_27321634 Human_Splice_Rec_445016,Human_Splice_Rec_445032 Human_miRNA_ID_2383899 RMVar_hsa_circ_76920,RMVar_hsa_circ_219107,RMVar_hsa_circ_219108 87625 RMVar_ID_87625 Human_SNP_ID_134581246 m1A Human chr3 - 57597198 57597198 57597198 CGTTTAGTTTGCCTGGGAGCTTGAAAGGAGAAAGCACGGGGTCGCCCCAAACCCCTTCTGCTTCT CGTTTAGTTTGCCTGGGAGCTTGAAAGGAGAAGGCACGGGGTCGCCCCAAACCCCTTCTGCTTCT T C ARF4 Ensembl:ENSG00000168374 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:57597148..57597402 26863196 MeRIP-seq:(Medium) rs1385993075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68779,Human_RBP_ID_936567,Human_RBP_ID_4758148,Human_RBP_ID_5530951,Human_RBP_ID_7214545,Human_RBP_ID_8577135,Human_RBP_ID_14909365,Human_RBP_ID_20930193,Human_RBP_ID_22398755,Human_RBP_ID_22824795,Human_RBP_ID_24013831,Human_RBP_ID_27058018 Human_Splice_Rec_445016,Human_Splice_Rec_445032 RMVar_hsa_circ_76920,RMVar_hsa_circ_219107,RMVar_hsa_circ_219108 87626 RMVar_ID_87626 Human_SNP_ID_134605543 m1A Human chr3 - 57692911 57692910 57692911 GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGGAGGCGCGCCAGAGGACGATGAAGAGGACGATGG GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGG_GGCGCGCCAGAGGACGATGAAGAGGACGATGG CT C DENND6A Ensembl:ENSG00000174839 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:57692867..57693053 26863196 MeRIP-seq:(Medium) rs1369597885 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4758153,Human_RBP_ID_23026636 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219128 87627 RMVar_ID_87627 Human_SNP_ID_134605544 m1A Human chr3 - 57692911 57692911 57692911 GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGGAGGCGCGCCAGAGGACGATGAAGAGGACGATGG GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGGGGGCGCGCCAGAGGACGATGAAGAGGACGATGG T C DENND6A Ensembl:ENSG00000174839 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:57692867..57693053 26863196 MeRIP-seq:(Medium) rs61737717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758153,Human_RBP_ID_23026636 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219128 87628 RMVar_ID_87628 Human_SNP_ID_134605551 m1A Human chr3 + 57692921 57692921 57692921 CTTCATCGTCCTCTGGCGCGCCTCCCGCCGCCACAAGGGCCGGCGCCTCGCGGCCCTCGGCCCCT CTTCATCGTCCTCTGGCGCGCCTCCCGCCGCCGCAAGGGCCGGCGCCTCGCGGCCCTCGGCCCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:57692883..57693049 26863196 MeRIP-seq:(Medium) rs1296372688 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 87629 RMVar_ID_87629 Human_SNP_ID_134621598 m1A Human chr3 + 57756341 57756341 57756341 AGTCAGAGTCACTATGGCGGCCGGCGCTGGCAAGGTAAGCTGAGGCGGTGGTGGCGGCTAGGGAG AGTCAGAGTCACTATGGCGGCCGGCGCTGGCAGGGTAAGCTGAGGCGGTGGTGGCGGCTAGGGAG A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:57756325..57756412 26863196 MeRIP-seq:(Medium) rs1180474248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248420,Human_RBP_ID_18424002,Human_RBP_ID_22284969 Human_Splice_Rec_445117,Human_Splice_Rec_445159,Human_Splice_Rec_445203,Human_Splice_Rec_445247 87630 RMVar_ID_87630 Human_SNP_ID_134662525 m1A Human chr3 - 57925912 57925912 57925912 GTGCTTGTACCTTTCTCTACCACAATGGACCGAAACACCAAAACAGGAAAGCCAGGAATAGGCCG GTGCTTGTACCTTTCTCTACCACAATGGACCGCAACACCAAAACAGGAAAGCCAGGAATAGGCCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:57925863..57925964 32194978 MeRIP-seq:(Medium) rs1416199715 Functional Loss SNV dbSNP153 33..33 33 - - - 87631 RMVar_ID_87631 Human_SNP_ID_134694885 m1A Human chr3 - 58057557 58057557 58057557 CTGTTAGCTGCCTCTAAGTTGTTCCCTAGCCCAGCAGCCATCATCTAATGTCAGGCCCCTTTACT CTGTTAGCTGCCTCTAAGTTGTTCCCTAGCCCGGCAGCCATCATCTAATGTCAGGCCCCTTTACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:58057536..58057740 26863196 MeRIP-seq:(Medium) rs936369393 Functional Loss SNV dbSNP153 33..33 33 - - - 87632 RMVar_ID_87632 Human_SNP_ID_134700085 m1A Human chr3 - 58078766 58078766 58078766 CAGTCATCTGCCTGCTGCATGGCTTCTCGTGCATTATCCACAGGCTTCTGCGGGTCCCAGGATTC CAGTCATCTGCCTGCTGCATGGCTTCTCGTGCGTTATCCACAGGCTTCTGCGGGTCCCAGGATTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:58078701..58078825 32194978 MeRIP-seq:(Medium) rs1274950884 Functional Loss SNV dbSNP153 33..33 33 - - - 87633 RMVar_ID_87633 Human_SNP_ID_134704975 m1A Human chr3 + 58098759 58098759 58098759 CATTGGTGTGGAGGTGGAAGATCCCCAGGGGAAGAACACCGTGGAGTTGCTCGTGGAAGACAAAG CATTGGTGTGGAGGTGGAAGATCCCCAGGGGAGGAACACCGTGGAGTTGCTCGTGGAAGACAAAG A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:58098683..58098797 26863196 MeRIP-seq:(Medium) rs145673747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835741,Human_RBP_ID_937371,Human_RBP_ID_3964137,Human_RBP_ID_5602781,Human_RBP_ID_8236051,Human_RBP_ID_8875542,Human_RBP_ID_18471695,Human_RBP_ID_22455986,Human_RBP_ID_26347020 Human_Splice_Rec_445826,Human_Splice_Rec_445918,Human_Splice_Rec_446006,Human_Splice_Rec_446096,Human_Splice_Rec_446184 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_357220,RMVar_hsa_circ_90360,RMVar_hsa_circ_101694,RMVar_hsa_circ_111111,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_77314,RMVar_hsa_circ_112703,RMVar_hsa_circ_219171,RMVar_hsa_circ_219173,RMVar_hsa_circ_219174,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_89284,RMVar_hsa_circ_219178,RMVar_hsa_circ_219179,RMVar_hsa_circ_120138,RMVar_hsa_circ_85416,RMVar_hsa_circ_219180,RMVar_hsa_circ_219181,RMVar_hsa_circ_219182,RMVar_hsa_circ_119261,RMVar_hsa_circ_122972,RMVar_hsa_circ_219184,RMVar_hsa_circ_354872,RMVar_hsa_circ_51724,RMVar_hsa_circ_70629,RMVar_hsa_circ_15821,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_359080,RMVar_hsa_circ_91076,RMVar_hsa_circ_94256,RMVar_hsa_circ_122115,RMVar_hsa_circ_219188,RMVar_hsa_circ_219189,RMVar_hsa_circ_119463,RMVar_hsa_circ_87303,RMVar_hsa_circ_89259,RMVar_hsa_circ_80465,RMVar_hsa_circ_219191,RMVar_hsa_circ_219193,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_219194,RMVar_hsa_circ_219192,RMVar_hsa_circ_219190 87634 RMVar_ID_87634 Human_SNP_ID_134706027 m1A Human chr3 + 58102252 58102252 58102252 TGCCGGGCCAGTGGCCGAGGCCTACAACCCAAAGGCGTCCGTATCCGGGAGACCACAGATTTCAA TGCCGGGCCAGTGGCCGAGGCCTACAACCCAAGGGCGTCCGTATCCGGGAGACCACAGATTTCAA A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:58102201..58102350 32194978 MeRIP-seq:(Medium) rs776814664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247327,Human_RBP_ID_3965362,Human_RBP_ID_5530550,Human_RBP_ID_8875063,Human_RBP_ID_9302362 Human_Splice_Rec_445828,Human_Splice_Rec_445829,Human_Splice_Rec_445920,Human_Splice_Rec_445921,Human_Splice_Rec_446008,Human_Splice_Rec_446009,Human_Splice_Rec_446098,Human_Splice_Rec_446099,Human_Splice_Rec_446186,Human_Splice_Rec_446187 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_90360,RMVar_hsa_circ_101694,RMVar_hsa_circ_111111,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_77314,RMVar_hsa_circ_112703,RMVar_hsa_circ_219171,RMVar_hsa_circ_219173,RMVar_hsa_circ_219174,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_89284,RMVar_hsa_circ_219178,RMVar_hsa_circ_219179,RMVar_hsa_circ_120138,RMVar_hsa_circ_85416,RMVar_hsa_circ_219180,RMVar_hsa_circ_219181,RMVar_hsa_circ_219182,RMVar_hsa_circ_119261,RMVar_hsa_circ_122972,RMVar_hsa_circ_219184,RMVar_hsa_circ_51724,RMVar_hsa_circ_70629,RMVar_hsa_circ_15821,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_359080,RMVar_hsa_circ_91076,RMVar_hsa_circ_94256,RMVar_hsa_circ_219188,RMVar_hsa_circ_219189,RMVar_hsa_circ_119463,RMVar_hsa_circ_87303,RMVar_hsa_circ_89259,RMVar_hsa_circ_80465,RMVar_hsa_circ_98479,RMVar_hsa_circ_219191,RMVar_hsa_circ_219193,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_219194,RMVar_hsa_circ_219192,RMVar_hsa_circ_269448,RMVar_hsa_circ_3982,RMVar_hsa_circ_53706,RMVar_hsa_circ_219197 87635 RMVar_ID_87635 Human_SNP_ID_134706855 m1A Human chr3 - 58105200 58105200 58105200 AGCTGTGTCCACTTACCCAGAGACCCCACTTCAGAGCCAATGGATTCTACCACGAAGTCCGCTGA AGCTGTGTCCACTTACCCAGAGACCCCACTTCGGAGCCAATGGATTCTACCACGAAGTCCGCTGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:58105176..58105200 32194978 MeRIP-seq:(Medium) rs1157652143 Functional Loss SNV dbSNP153 33..33 33 - - - 87636 RMVar_ID_87636 Human_SNP_ID_134711606 m1A Human chr3 + 58123446 58123446 58123446 GAAGCTGGCCTCCTTAGCGTCGACTGCTCGGAAGCGGGACCGGGGGCCCTGGGCCTGGAAGCTGT GAAGCTGGCCTCCTTAGCGTCGACTGCTCGGAGGCGGGACCGGGGGCCCTGGGCCTGGAAGCTGT A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:58123400..58123503 26863196 MeRIP-seq:(Medium) rs774898478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937389,Human_RBP_ID_4751733,Human_RBP_ID_5530565,Human_RBP_ID_8875072,Human_RBP_ID_9302373,Human_RBP_ID_17292410,Human_RBP_ID_18194907,Human_RBP_ID_22456001 Human_miRNA_ID_731048,Human_miRNA_ID_2294990,Human_miRNA_ID_2572358 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_90360,RMVar_hsa_circ_111111,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_9008,RMVar_hsa_circ_112703,RMVar_hsa_circ_219171,RMVar_hsa_circ_219173,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_219178,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_70629,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_17572,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_53706,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_295896,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_126525,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219203,RMVar_hsa_circ_219206,RMVar_hsa_circ_115414,RMVar_hsa_circ_219207,RMVar_hsa_circ_219208,RMVar_hsa_circ_83988,RMVar_hsa_circ_219212,RMVar_hsa_circ_78034,RMVar_hsa_circ_219213,RMVar_hsa_circ_126764,RMVar_hsa_circ_65074,RMVar_hsa_circ_20161,RMVar_hsa_circ_219214,RMVar_hsa_circ_219215,RMVar_hsa_circ_276002,RMVar_hsa_circ_123318,RMVar_hsa_circ_45616,RMVar_hsa_circ_41743,RMVar_hsa_circ_62470,RMVar_hsa_circ_219216,RMVar_hsa_circ_219217,RMVar_hsa_circ_68638,RMVar_hsa_circ_362730,RMVar_hsa_circ_114091,RMVar_hsa_circ_356300,RMVar_hsa_circ_369422,RMVar_hsa_circ_353500,RMVar_hsa_circ_76358,RMVar_hsa_circ_219219,RMVar_hsa_circ_219220,RMVar_hsa_circ_219221 87637 RMVar_ID_87637 Human_SNP_ID_134712604 m1A Human chr3 + 58126713 58126712 58126713 GGCAGCTGCAGTGCTGAGTACATTCCTTTCGCACCGGGGGATTACGATGTTAATATCACATATGG GGCAGCTGCAGTGCTGAGTACATTCCTTTCGTGCCGGGGGATTACGATGTTAATATCACATATGG CA TG FLNB Ensembl:ENSG00000136068 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1559713654 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_67586,Human_RBP_ID_8874038,Human_RBP_ID_9261136 Human_Splice_Rec_445859,Human_Splice_Rec_445951,Human_Splice_Rec_446039,Human_Splice_Rec_446129,Human_Splice_Rec_446217 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_90360,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_9008,RMVar_hsa_circ_219171,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_295896,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_126525,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219203,RMVar_hsa_circ_219206,RMVar_hsa_circ_115414,RMVar_hsa_circ_219207,RMVar_hsa_circ_219208,RMVar_hsa_circ_83988,RMVar_hsa_circ_219212,RMVar_hsa_circ_78034,RMVar_hsa_circ_219213,RMVar_hsa_circ_126764,RMVar_hsa_circ_65074,RMVar_hsa_circ_20161,RMVar_hsa_circ_219214,RMVar_hsa_circ_219215,RMVar_hsa_circ_276002,RMVar_hsa_circ_123318,RMVar_hsa_circ_45616,RMVar_hsa_circ_128181,RMVar_hsa_circ_62470,RMVar_hsa_circ_219216,RMVar_hsa_circ_219217,RMVar_hsa_circ_362730,RMVar_hsa_circ_114091,RMVar_hsa_circ_356300,RMVar_hsa_circ_369422,RMVar_hsa_circ_353500,RMVar_hsa_circ_76358,RMVar_hsa_circ_219219,RMVar_hsa_circ_219220,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_287080,RMVar_hsa_circ_268944,RMVar_hsa_circ_219223,RMVar_hsa_circ_76324,RMVar_hsa_circ_92411,RMVar_hsa_circ_219225,RMVar_hsa_circ_219226,RMVar_hsa_circ_219224,RMVar_hsa_circ_85139,RMVar_hsa_circ_93933,RMVar_hsa_circ_219228,RMVar_hsa_circ_219229 87638 RMVar_ID_87638 Human_SNP_ID_134712605 m1A Human chr3 + 58126713 58126713 58126713 GGCAGCTGCAGTGCTGAGTACATTCCTTTCGCACCGGGGGATTACGATGTTAATATCACATATGG GGCAGCTGCAGTGCTGAGTACATTCCTTTCGCGCCGGGGGATTACGATGTTAATATCACATATGG A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2362903 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_67586,Human_RBP_ID_8874038,Human_RBP_ID_9261136 Human_Splice_Rec_445859,Human_Splice_Rec_445951,Human_Splice_Rec_446039,Human_Splice_Rec_446129,Human_Splice_Rec_446217 Clinvar_Rec_484 GWAS_ID_10845 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_90360,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_9008,RMVar_hsa_circ_219171,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_295896,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_126525,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219203,RMVar_hsa_circ_219206,RMVar_hsa_circ_115414,RMVar_hsa_circ_219207,RMVar_hsa_circ_219208,RMVar_hsa_circ_83988,RMVar_hsa_circ_219212,RMVar_hsa_circ_78034,RMVar_hsa_circ_219213,RMVar_hsa_circ_126764,RMVar_hsa_circ_65074,RMVar_hsa_circ_20161,RMVar_hsa_circ_219214,RMVar_hsa_circ_219215,RMVar_hsa_circ_276002,RMVar_hsa_circ_123318,RMVar_hsa_circ_45616,RMVar_hsa_circ_128181,RMVar_hsa_circ_62470,RMVar_hsa_circ_219216,RMVar_hsa_circ_219217,RMVar_hsa_circ_362730,RMVar_hsa_circ_114091,RMVar_hsa_circ_356300,RMVar_hsa_circ_369422,RMVar_hsa_circ_353500,RMVar_hsa_circ_76358,RMVar_hsa_circ_219219,RMVar_hsa_circ_219220,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_287080,RMVar_hsa_circ_268944,RMVar_hsa_circ_219223,RMVar_hsa_circ_76324,RMVar_hsa_circ_92411,RMVar_hsa_circ_219225,RMVar_hsa_circ_219226,RMVar_hsa_circ_219224,RMVar_hsa_circ_85139,RMVar_hsa_circ_93933,RMVar_hsa_circ_219228,RMVar_hsa_circ_219229 87639 RMVar_ID_87639 Human_SNP_ID_134715011 m1A Human chr3 - 58136076 58136072 58136076 GTGGGATGTCGTCACCCCCGTAGGTGACTCCAATCATATAGCGCCCAGTCTTGTCGGGGATGTAG GTGGGATGTCGTCACCCCCGTAGGTGACTCCA____TATAGCGCCCAGTCTTGTCGGGGATGTAG ATGAT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58135976..58136075 32194978 MeRIP-seq:(Medium) rs1553703909 Functional Loss DEL dbSNP153 33..36 33 - - - Clinvar_Rec_485 87640 RMVar_ID_87640 Human_SNP_ID_134717512 m1A Human chr3 - 58146019 58146019 58146019 ACCTTCTCCTGCATCCTCTGTGACGATGGTGAAGGTGGCAGTTTTGTTGGCCACTCCATACACGA ACCTTCTCCTGCATCCTCTGTGACGATGGTGAGGGTGGCAGTTTTGTTGGCCACTCCATACACGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58145901..58146050 32194978 MeRIP-seq:(Medium) rs1178860596 Functional Loss SNV dbSNP153 33..33 33 - - - 87641 RMVar_ID_87641 Human_SNP_ID_134718083 m1A Human chr3 + 58148326 58148326 58148326 GGCCAGCATTAAGGCCCCATCTGGCCGAGACGAGCCCTGTCTCCTGAAGAGGCTGCCCAACAACC GGCCAGCATTAAGGCCCCATCTGGCCGAGACGGGCCCTGTCTCCTGAAGAGGCTGCCCAACAACC A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58148301..58148325 32194978 MeRIP-seq:(Medium) rs111560302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8875089,Human_RBP_ID_22456031 Human_Splice_Rec_445883,Human_Splice_Rec_445971,Human_Splice_Rec_446061,Human_Splice_Rec_446151,Human_Splice_Rec_446237,Human_Splice_Rec_446275 RMVar_hsa_circ_92492,RMVar_hsa_circ_219168,RMVar_hsa_circ_96548,RMVar_hsa_circ_219169,RMVar_hsa_circ_116455,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_219186,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_123318,RMVar_hsa_circ_219235,RMVar_hsa_circ_219216,RMVar_hsa_circ_76358,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_93933,RMVar_hsa_circ_219229,RMVar_hsa_circ_104236,RMVar_hsa_circ_81753,RMVar_hsa_circ_285374,RMVar_hsa_circ_219230,RMVar_hsa_circ_267721,RMVar_hsa_circ_325376,RMVar_hsa_circ_370760,RMVar_hsa_circ_108769,RMVar_hsa_circ_99458,RMVar_hsa_circ_91283,RMVar_hsa_circ_78061,RMVar_hsa_circ_219237,RMVar_hsa_circ_219238,RMVar_hsa_circ_219236,RMVar_hsa_circ_7589,RMVar_hsa_circ_219231,RMVar_hsa_circ_219233,RMVar_hsa_circ_219234,RMVar_hsa_circ_219232,RMVar_hsa_circ_106405,RMVar_hsa_circ_219246,RMVar_hsa_circ_20324,RMVar_hsa_circ_219252,RMVar_hsa_circ_52027,RMVar_hsa_circ_46728,RMVar_hsa_circ_294460,RMVar_hsa_circ_369490,RMVar_hsa_circ_373307,RMVar_hsa_circ_312754,RMVar_hsa_circ_59015,RMVar_hsa_circ_219250,RMVar_hsa_circ_219251,RMVar_hsa_circ_219249,RMVar_hsa_circ_12780,RMVar_hsa_circ_93955,RMVar_hsa_circ_219253 87642 RMVar_ID_87642 Human_SNP_ID_134718084 m1A Human chr3 + 58148326 58148326 58148326 GGCCAGCATTAAGGCCCCATCTGGCCGAGACGAGCCCTGTCTCCTGAAGAGGCTGCCCAACAACC GGCCAGCATTAAGGCCCCATCTGGCCGAGACGTGCCCTGTCTCCTGAAGAGGCTGCCCAACAACC A T FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58148301..58148325 32194978 MeRIP-seq:(Medium) rs111560302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8875089,Human_RBP_ID_22456031 Human_Splice_Rec_445883,Human_Splice_Rec_445971,Human_Splice_Rec_446061,Human_Splice_Rec_446151,Human_Splice_Rec_446237,Human_Splice_Rec_446275 RMVar_hsa_circ_92492,RMVar_hsa_circ_219168,RMVar_hsa_circ_96548,RMVar_hsa_circ_219169,RMVar_hsa_circ_116455,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_219186,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_123318,RMVar_hsa_circ_219235,RMVar_hsa_circ_219216,RMVar_hsa_circ_76358,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_93933,RMVar_hsa_circ_219229,RMVar_hsa_circ_104236,RMVar_hsa_circ_81753,RMVar_hsa_circ_285374,RMVar_hsa_circ_219230,RMVar_hsa_circ_267721,RMVar_hsa_circ_325376,RMVar_hsa_circ_370760,RMVar_hsa_circ_108769,RMVar_hsa_circ_99458,RMVar_hsa_circ_91283,RMVar_hsa_circ_78061,RMVar_hsa_circ_219237,RMVar_hsa_circ_219238,RMVar_hsa_circ_219236,RMVar_hsa_circ_7589,RMVar_hsa_circ_219231,RMVar_hsa_circ_219233,RMVar_hsa_circ_219234,RMVar_hsa_circ_219232,RMVar_hsa_circ_106405,RMVar_hsa_circ_219246,RMVar_hsa_circ_20324,RMVar_hsa_circ_219252,RMVar_hsa_circ_52027,RMVar_hsa_circ_46728,RMVar_hsa_circ_294460,RMVar_hsa_circ_369490,RMVar_hsa_circ_373307,RMVar_hsa_circ_312754,RMVar_hsa_circ_59015,RMVar_hsa_circ_219250,RMVar_hsa_circ_219251,RMVar_hsa_circ_219249,RMVar_hsa_circ_12780,RMVar_hsa_circ_93955,RMVar_hsa_circ_219253 87643 RMVar_ID_87643 Human_SNP_ID_134718591 m1A Human chr3 - 58150018 58150018 58150018 TACAGAAAACCCAAGCATCCCACCTGGAGGGGAATGGAATGCACATACCAGGCACGTGCTCGTCA TACAGAAAACCCAAGCATCCCACCTGGAGGGGCATGGAATGCACATACCAGGCACGTGCTCGTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:58150016..58150083 26863196 MeRIP-seq:(Medium) rs747902703 Functional Loss SNV dbSNP153 33..33 33 - - - 87644 RMVar_ID_87644 Human_SNP_ID_134720242 m1A Human chr3 - 58156062 58156062 58156062 ATGCTTCCTTGCATCTCACCTGAAGGCTCATAACAGTGAGGCGGCGGGCGTCGTCGGAGGGTGCG ATGCTTCCTTGCATCTCACCTGAAGGCTCATAGCAGTGAGGCGGCGGGCGTCGTCGGAGGGTGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:58156011..58156116 26863196 MeRIP-seq:(Medium) rs1291684975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219259 87645 RMVar_ID_87645 Human_SNP_ID_134723081 m1A Human chr3 - 58168626 58168626 58168626 CTGTCACCTTGGCCTTGAAGGGACTGCCCACGATGTGGTTGGGCCCACCGTATTTGACGCTGATC CTGTCACCTTGGCCTTGAAGGGACTGCCCACGGTGTGGTTGGGCCCACCGTATTTGACGCTGATC T C FLNB-AS1 Ensembl:ENSG00000244161 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:58168576..58168675 32194978 MeRIP-seq:(Medium) rs1483188324 Functional Loss SNV dbSNP153 33..33 33 - - - 87646 RMVar_ID_87646 Human_SNP_ID_134723819 m1A Human chr3 + 58171298 58171298 58171298 CTGCTTTACCGCTCCTCATCGCCAACACCCCCATGCTCTGTGGCCTTCTTACACTTCTCAGAGGG CTGCTTTACCGCTCCTCATCGCCAACACCCCCGTGCTCTGTGGCCTTCTTACACTTCTCAGAGGG A G FLNB Ensembl:ENSG00000136068 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58170951..58171300 32194978 MeRIP-seq:(Medium) rs1023211438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606881,Human_RBP_ID_8577324,Human_RBP_ID_17292411,Human_RBP_ID_17521578 RMVar_hsa_circ_267721 87647 RMVar_ID_87647 Human_SNP_ID_134741082 m1A Human chr3 + 58237839 58237839 58237839 GCTGGGAGCGGCGCGGGTAGGAGCCCGGCGGCAGGTCCCAGCCCGGGGCTAGAGACCGAGGGCCG GCTGGGAGCGGCGCGGGTAGGAGCCCGGCGGCTGGTCCCAGCCCGGGGCTAGAGACCGAGGGCCG A T ABHD6 Ensembl:ENSG00000163686 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:58237552..58237946;chr3:58237580..58237930;chr3:58237557..58237930 26863196 MeRIP-seq:(Medium) rs1452434448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756571 Human_Splice_Rec_446401,Human_Splice_Rec_446417,Human_Splice_Rec_446435 RMVar_hsa_circ_219261,RMVar_hsa_circ_77795 87648 RMVar_ID_87648 Human_SNP_ID_134751893 m1A Human chr3 + 58283705 58283705 58283705 GATGGATGGATGGGAGGATATCTGGTTAATGCAGAGATGGAGGTTGGATGGATTGATGAATACAG GATGGATGGATGGGAGGATATCTGGTTAATGCTGAGATGGAGGTTGGATGGATTGATGAATACAG A T ABHD6 Ensembl:ENSG00000163686 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:58283693..58283871 26863196 MeRIP-seq:(Medium) rs1306679112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14914785 RMVar_hsa_circ_290823,RMVar_hsa_circ_267483,RMVar_hsa_circ_219262,RMVar_hsa_circ_374093,RMVar_hsa_circ_219266,RMVar_hsa_circ_327361,RMVar_hsa_circ_219270,RMVar_hsa_circ_219272,RMVar_hsa_circ_90029,RMVar_hsa_circ_294673,RMVar_hsa_circ_219271 87649 RMVar_ID_87649 Human_SNP_ID_134765292 m1A Human chr3 - 58332982 58332982 58332982 GCTGGCGGCTTCTCCATGAAGGCCATCCCGGGACGCCCGGCCGCCGCCGCCTAGGGACGCGAGGT GCTGGCGGCTTCTCCATGAAGGCCATCCCGGGCCGCCCGGCCGCCGCCGCCTAGGGACGCGAGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:58332932..58333060 26863196 MeRIP-seq:(Medium) rs1437056100 Functional Loss SNV dbSNP153 33..33 33 - - - 87650 RMVar_ID_87650 Human_SNP_ID_134788550 m1A Human chr3 + 58426896 58426893 58426896 GTTTTCTACCCACATTGACTTTTTTTTTTTCTATCTATCTTTTCTTTGTAGAGATGGGGTTTTGC GTTTTCTACCCACATTGACTTTTTTTTTTT___TCTATCTTTTCTTTGTAGAGATGGGGTTTTGC TCTA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:58426852..58427024 26863196 MeRIP-seq:(Medium) rs1276365653 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_7216124 87651 RMVar_ID_87651 Human_SNP_ID_134788555 m1A Human chr3 + 58426896 58426896 58426896 GTTTTCTACCCACATTGACTTTTTTTTTTTCTATCTATCTTTTCTTTGTAGAGATGGGGTTTTGC GTTTTCTACCCACATTGACTTTTTTTTTTTCTTTCTATCTTTTCTTTGTAGAGATGGGGTTTTGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:58426852..58427024 26863196 MeRIP-seq:(Medium) rs13076826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7216124 87652 RMVar_ID_87652 Human_SNP_ID_134788578 m1A Human chr3 - 58426949 58426949 58426949 GAGGTGGGTGGATCCCTTGAGTGTAGGAGTTCAGGACCAGCCTGGGGAACATGGCAAAACCCCAT GAGGTGGGTGGATCCCTTGAGTGTAGGAGTTCGGGACCAGCCTGGGGAACATGGCAAAACCCCAT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:58426910..58427048 26863196 MeRIP-seq:(Medium) rs1256461855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7216125,Human_RBP_ID_14916892,Human_RBP_ID_25771691 87653 RMVar_ID_87653 Human_SNP_ID_134789752 m1A Human chr3 - 58430927 58430927 58430927 CGTTTTTGATTTTACAGGCTGGGTTGCGGCCCATTTGTGAATTTATGACCTTCAATTTCTCCATG CGTTTTTGATTTTACAGGCTGGGTTGCGGCCCCTTTGTGAATTTATGACCTTCAATTTCTCCATG T G PDHB Ensembl:ENSG00000168291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:58430877..58430978 26863196 MeRIP-seq:(Medium) rs779872594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22456807,Human_RBP_ID_22678718,Human_RBP_ID_24014644 Human_Splice_Rec_446914,Human_Splice_Rec_446930,Human_Splice_Rec_446948,Human_Splice_Rec_446966,Human_Splice_Rec_446967,Human_Splice_Rec_446992,Human_Splice_Rec_447008,Human_Splice_Rec_447024 Human_miRNA_ID_1424172,Human_miRNA_ID_2727295 RMVar_hsa_circ_33368,RMVar_hsa_circ_309160,RMVar_hsa_circ_219287,RMVar_hsa_circ_45992,RMVar_hsa_circ_219286,RMVar_hsa_circ_86460 87654 RMVar_ID_87654 Human_SNP_ID_134790075 m1A Human chr3 - 58431959 58431957 58431959 GTGACAGGTGACAGTTCGTGATGCTATAAATCAGGGTATGGATGAGGAGCTGGAAAGAGATGAGA GTGACAGGTGACAGTTCGTGATGCTATAAATC__GGTATGGATGAGGAGCTGGAAAGAGATGAGA CCT C PDHB Ensembl:ENSG00000168291 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:58431751..58432032;chr3:58431726..58432020;chr3:58431576..58432031;chr3:58431601..58432040 26863196 MeRIP-seq:(Medium) rs778727916 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_607014,Human_RBP_ID_1034059,Human_RBP_ID_1313976,Human_RBP_ID_1966907,Human_RBP_ID_4757339,Human_RBP_ID_7216145,Human_RBP_ID_14916953,Human_RBP_ID_18812982,Human_RBP_ID_20971233,Human_RBP_ID_24014649,Human_RBP_ID_27822342 Human_Splice_Rec_446908,Human_Splice_Rec_446909,Human_Splice_Rec_446924,Human_Splice_Rec_446925,Human_Splice_Rec_446942,Human_Splice_Rec_446943,Human_Splice_Rec_446960,Human_Splice_Rec_446961,Human_Splice_Rec_446979,Human_Splice_Rec_446986,Human_Splice_Rec_446987,Human_Splice_Rec_447002,Human_Splice_Rec_447003,Human_Splice_Rec_447020,Human_Splice_Rec_447030,Human_Splice_Rec_447031,Human_Splice_Rec_447038,Human_Splice_Rec_447039 RMVar_hsa_circ_33368,RMVar_hsa_circ_219287,RMVar_hsa_circ_86460,RMVar_hsa_circ_219288,RMVar_hsa_circ_322520 87655 RMVar_ID_87655 Human_SNP_ID_134804529 m1A Human chr3 + 58492152 58492152 58492152 CGGCCGCGGGCATCTCCCGGCCCGGCCGCAGCAGCCGCCGCCGCCGCGCAGTGAGTGGGGCTGGC CGGCCGCGGGCATCTCCCGGCCCGGCCGCAGCCGCCGCCGCCGCCGCGCAGTGAGTGGGGCTGGC A C KCTD6 Ensembl:ENSG00000168301 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr3:58492117..58492204;chr3:58492088..58492571 26863410,26863196 MeRIP-seq:(Medium) rs1213763937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758170 Human_Splice_Rec_447041,Human_Splice_Rec_447045,Human_Splice_Rec_447051 87656 RMVar_ID_87656 Human_SNP_ID_134804530 m1A Human chr3 + 58492152 58492152 58492152 CGGCCGCGGGCATCTCCCGGCCCGGCCGCAGCAGCCGCCGCCGCCGCGCAGTGAGTGGGGCTGGC CGGCCGCGGGCATCTCCCGGCCCGGCCGCAGCGGCCGCCGCCGCCGCGCAGTGAGTGGGGCTGGC A G KCTD6 Ensembl:ENSG00000168301 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr3:58492117..58492204;chr3:58492088..58492571 26863410,26863196 MeRIP-seq:(Medium) rs1213763937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758170 Human_Splice_Rec_447041,Human_Splice_Rec_447045,Human_Splice_Rec_447051 87657 RMVar_ID_87657 Human_SNP_ID_134946385 m1A Human chr3 + 59049879 59049879 59049879 GCCTCCGCGGTGCCCGGGTCTGGGGAGGGCGCAGCTGCCTGGACGGACTCCGGGCCGTCCCTGGG GCCTCCGCGGTGCCCGGGTCTGGGGAGGGCGCGGCTGCCTGGACGGACTCCGGGCCGTCCCTGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:59049829..59049932 26863196 MeRIP-seq:(Medium) rs1269304285 Functional Loss SNV dbSNP153 33..33 33 - - - 87658 RMVar_ID_87658 Human_SNP_ID_510985778 m1A Human chr12 + 91182755 91182754 91182755 AAGTAAAAGAGTTTGCAGGTGTGGAAAGGAGGAGGGGGTAGGTGCTGCTCTGTGACTAGGTTGAA AAGTAAAAGAGTTTGCAGGTGTGGAAAGGAGG_GGGGGTAGGTGCTGCTCTGTGACTAGGTTGAA GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:91182592..91182755 26863196 MeRIP-seq:(Medium) rs1157433810 Functional Loss DEL dbSNP153 33..33 33 - - - 87659 RMVar_ID_87659 Human_SNP_ID_511211996 m1A Human chr12 - 92145546 92145546 92145546 GCCGAGCCCCAGCCGCCCCGGGCCGCCCCCGCACGCCGCCCCCATGCATCCCTTCTACACCCGGG GCCGAGCCCCAGCCGCCCCGGGCCGCCCCCGCGCGCCGCCCCCATGCATCCCTTCTACACCCGGG T C BTG1 Ensembl:ENSG00000133639 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr12:92145451..92145723;chr12:92145426..92145798 26863196,26863410 MeRIP-seq:(Medium) rs1173859899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755645,Human_RBP_ID_4246232,Human_RBP_ID_17357290,Human_RBP_ID_22532507 87660 RMVar_ID_87660 Human_SNP_ID_511211997 m1A Human chr12 - 92145546 92145546 92145546 GCCGAGCCCCAGCCGCCCCGGGCCGCCCCCGCACGCCGCCCCCATGCATCCCTTCTACACCCGGG GCCGAGCCCCAGCCGCCCCGGGCCGCCCCCGCCCGCCGCCCCCATGCATCCCTTCTACACCCGGG T G BTG1 Ensembl:ENSG00000133639 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr12:92145451..92145723;chr12:92145426..92145798 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_755645,Human_RBP_ID_4246232,Human_RBP_ID_17357290,Human_RBP_ID_22532507 87661 RMVar_ID_87661 Human_SNP_ID_511212039 m1A Human chr12 + 92145601 92145601 92145601 GGGGCTCGGCGGCGCGGCCCCGACGGCGGAGCAGCCACCCCGGGCTTCCTCACCGGGCGGAAGGC GGGGCTCGGCGGCGCGGCCCCGACGGCGGAGCTGCCACCCCGGGCTTCCTCACCGGGCGGAAGGC A T AC025164.2 Ensembl:ENSG00000245904 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:92145501..92145775 26863410 MeRIP-seq:(Medium) rs1169996694 Functional Loss SNV dbSNP153 33..33 33 - - - 87662 RMVar_ID_87662 Human_SNP_ID_511212075 m1A Human chr12 - 92145687 92145687 92145687 GCCTCCTGTCTCGAAAATAACTTTTTTAGTCTAAAGAAAGAAAGACAAAAGTAGTCGTCCGCCCC GCCTCCTGTCTCGAAAATAACTTTTTTAGTCTGAAGAAAGAAAGACAAAAGTAGTCGTCCGCCCC T C BTG1 Ensembl:ENSG00000133639 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:92145450..92145699 32194978 MeRIP-seq:(Medium) rs1252097823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4244046,Human_RBP_ID_18634600 87663 RMVar_ID_87663 Human_SNP_ID_511397261 m1A Human chr12 + 92922259 92922259 92922259 TATCTTCTTCCCCAACATTTTCTTCCTCCTCTACCCTTAATCTTACATCTATTCCACCACCCTCA TATCTTCTTCCCCAACATTTTCTTCCTCCTCTGCCCTTAATCTTACATCTATTCCACCACCCTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:92922137..92922292 26863196 MeRIP-seq:(Medium) rs1157362897 Functional Loss SNV dbSNP153 33..33 33 - - - 87664 RMVar_ID_87664 Human_SNP_ID_511398988 m1A Human chr12 - 92929131 92929114 92929131 CCCGGCCCAGTCCCTCCCGCCCGCGCACCCCGAGTAGTGAGTGGCCCCGCGCAGGGTCTGGAGAG CCCGGCCCAGTCCCTCCCGCCCGCGCACCCCG_________________CGCAGGGTCTGGAGAG GCGGGGCCACTCACTACT G EEA1 Ensembl:ENSG00000102189 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:92929083..92929278 26863196 MeRIP-seq:(Medium) rs747850635 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_4247697,Human_RBP_ID_8787338,Human_RBP_ID_9279160 Human_Splice_Rec_1407337,Human_Splice_Rec_1407393,Human_Splice_Rec_1407433,Human_Splice_Rec_1407441 87665 RMVar_ID_87665 Human_SNP_ID_511398996 m1A Human chr12 - 92929131 92929131 92929131 CCCGGCCCAGTCCCTCCCGCCCGCGCACCCCGAGTAGTGAGTGGCCCCGCGCAGGGTCTGGAGAG CCCGGCCCAGTCCCTCCCGCCCGCGCACCCCGCGTAGTGAGTGGCCCCGCGCAGGGTCTGGAGAG T G EEA1 Ensembl:ENSG00000102189 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:92929083..92929278 26863196 MeRIP-seq:(Medium) rs1413908906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247697,Human_RBP_ID_8787338,Human_RBP_ID_9279160 Human_Splice_Rec_1407337,Human_Splice_Rec_1407393,Human_Splice_Rec_1407433,Human_Splice_Rec_1407441 87666 RMVar_ID_87666 Human_SNP_ID_511505683 m1A Human chr12 - 93377939 93377939 93377939 ACAGTTGCGAAGACCCGCTCCCACTGAGCAGCAGCACCGCGGCGACCGCGCGCCGCCCCCTCTGC ACAGTTGCGAAGACCCGCTCCCACTGAGCAGCGGCACCGCGGCGACCGCGCGCCGCCCCCTCTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:93377899..93378066 26863196 MeRIP-seq:(Medium) rs1006449022 Functional Loss SNV dbSNP153 33..33 33 - - - 87667 RMVar_ID_87667 Human_SNP_ID_511511094 m1A Human chr12 + 93398711 93398711 93398711 AGCAGTATGCCAGACTAATTTTTTTCCCTTGGAAAATGTGTCCATGGCTAGCTCCTGTAGATTAA AGCAGTATGCCAGACTAATTTTTTTCCCTTGGGAAATGTGTCCATGGCTAGCTCCTGTAGATTAA A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:93398708..93398779 26863196 MeRIP-seq:(Medium) rs769903197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377729 87668 RMVar_ID_87668 Human_SNP_ID_511528889 m1A Human chr12 - 93467556 93467556 93467556 GTCCTCGACAGGAGGAGTAGAGGGAAGCGGTTACCTTGACGGCTTCTCACCACGAACCCGCCATC GTCCTCGACAGGAGGAGTAGAGGGAAGCGGTTCCCTTGACGGCTTCTCACCACGAACCCGCCATC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:93467526..93467600 26863410 MeRIP-seq:(Medium) rs900999311 Functional Loss SNV dbSNP153 33..33 33 - - - 87669 RMVar_ID_87669 Human_SNP_ID_511553953 m1A Human chr12 - 93571638 93571638 93571638 ATTGCCTCGACCCCATCCCCCACCGCGCGGCGACGCCCCCTACGGGCTGGGACACCTCCACTCTC ATTGCCTCGACCCCATCCCCCACCGCGCGGCGTCGCCCCCTACGGGCTGGGACACCTCCACTCTC T A SOCS2-AS1 Ensembl:ENSG00000246985 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:93571597..93571675 26863196 MeRIP-seq:(Medium) rs1268803450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1407709,Human_Splice_Rec_1407723 87670 RMVar_ID_87670 Human_SNP_ID_511723240 m1A Human chr12 + 94294208 94294208 94294208 TTCCAGGGCTTCCCACCTCCCATCTGTCCCACAGGGTCCTGGCCTCCACCTTCTGCGTACTACCC TTCCAGGGCTTCCCACCTCCCATCTGTCCCACGGGGTCCTGGCCTCCACCTTCTGCGTACTACCC A G PLXNC1 Ensembl:ENSG00000136040 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:94294158..94294251 26863196 MeRIP-seq:(Medium) rs1326578181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31216 87671 RMVar_ID_87671 Human_SNP_ID_511730176 m1A Human chr12 + 94325056 94325056 94325056 GCTATTCCCTCTGGAACACCCTTACCTTACATATAACAACATGGCATCCTCCCTCCTTTCCTTCA GCTATTCCCTCTGGAACACCCTTACCTTACATGTAACAACATGGCATCCTCCCTCCTTTCCTTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:94325017..94325131 26863196 MeRIP-seq:(Medium) rs890836754 Functional Loss SNV dbSNP153 33..33 33 - - - 87672 RMVar_ID_87672 Human_SNP_ID_511761992 m1A Human chr12 - 94459790 94459790 94459790 GCCGCCGCCGCCGCCCTCGGACCTCTCCCGGGATACTTCACATTTCCCTAGGGACGGGAGCCCGA GCCGCCGCCGCCGCCCTCGGACCTCTCCCGGGGTACTTCACATTTCCCTAGGGACGGGAGCCCGA T C CEP83 Ensembl:ENSG00000173588 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:94459697..94459824 26863196 MeRIP-seq:(Medium) rs939222582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5417417,Human_RBP_ID_5438175,Human_RBP_ID_5462247,Human_RBP_ID_5492373,Human_RBP_ID_17829171,Human_RBP_ID_22178214,Human_RBP_ID_27425578 RMVar_hsa_circ_89775,RMVar_hsa_circ_158800 87673 RMVar_ID_87673 Human_SNP_ID_511883638 m1A Human chr12 - 94971454 94971454 94971454 GAAAGAAGATTCAGGAGTGGATCCCACCTTCAACACCTTACAAGTAAAGACAATGAAGAACAGTT GAAAGAAGATTCAGGAGTGGATCCCACCTTCAGCACCTTACAAGTAAAGACAATGAAGAACAGTT T C NDUFA12 Ensembl:ENSG00000184752 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:94971401..94971600 26863196 MeRIP-seq:(Medium) rs1362157816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430369,Human_RBP_ID_811723,Human_RBP_ID_995043,Human_RBP_ID_1358885,Human_RBP_ID_1803194,Human_RBP_ID_4260658,Human_RBP_ID_8247898,Human_RBP_ID_9023720,Human_RBP_ID_9365309,Human_RBP_ID_17241117,Human_RBP_ID_17356635,Human_RBP_ID_17474387,Human_RBP_ID_17829232,Human_RBP_ID_18526831,Human_RBP_ID_22437951,Human_RBP_ID_23579356,Human_RBP_ID_26323233,Human_RBP_ID_26616318,Human_RBP_ID_27219079,Human_RBP_ID_27426244,Human_RBP_ID_27635094 Human_Splice_Rec_1408242 Human_miRNA_ID_2977341 RMVar_hsa_circ_83213,RMVar_hsa_circ_92643,RMVar_hsa_circ_111874,RMVar_hsa_circ_90566,RMVar_hsa_circ_158819,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822,RMVar_hsa_circ_158820 87674 RMVar_ID_87674 Human_SNP_ID_511883654 m1A Human chr12 - 94971481 94971481 94971481 AACAATATGTACCTTATTCTACCACTAGAAAGAAGATTCAGGAGTGGATCCCACCTTCAACACCT AACAATATGTACCTTATTCTACCACTAGAAAGGAGATTCAGGAGTGGATCCCACCTTCAACACCT T C NDUFA12 Ensembl:ENSG00000184752 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:94971431..94971535 26863196 MeRIP-seq:(Medium) rs1198036202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9365309,Human_RBP_ID_17241924,Human_RBP_ID_17831034,Human_RBP_ID_22437951,Human_RBP_ID_26323233,Human_RBP_ID_26912630 Human_Splice_Rec_1408242 Human_miRNA_ID_2708761 RMVar_hsa_circ_83213,RMVar_hsa_circ_92643,RMVar_hsa_circ_111874,RMVar_hsa_circ_90566,RMVar_hsa_circ_158819,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822,RMVar_hsa_circ_158820 87675 RMVar_ID_87675 Human_SNP_ID_511883667 m1A Human chr12 + 94971534 94971534 94971534 GTACATATTGTTCTGGGGTGCCAGTCACGTTGAATTTATGGTTCGTCCAAATGAATTTACGAGCA GTACATATTGTTCTGGGGTGCCAGTCACGTTGGATTTATGGTTCGTCCAAATGAATTTACGAGCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:94971401..94971600 26863196 MeRIP-seq:(Medium) rs748785747 Functional Loss SNV dbSNP153 33..33 33 - - - 87676 RMVar_ID_87676 Human_SNP_ID_511889089 m1A Human chr12 - 94994238 94994238 94994238 TCTTCCCACCCAGGCCGTCACCGATGGGTTGTATATACTACTGAAATGAATGGCAAAAACACATT TCTTCCCACCCAGGCCGTCACCGATGGGTTGTGTATACTACTGAAATGAATGGCAAAAACACATT T C NDUFA12 Ensembl:ENSG00000184752 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:94994151..94994275 32194978 MeRIP-seq:(Medium) rs570041029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1478882,Human_RBP_ID_1803200,Human_RBP_ID_9323182,Human_RBP_ID_9365311,Human_RBP_ID_12060690,Human_RBP_ID_17241927,Human_RBP_ID_21884722,Human_RBP_ID_23579379,Human_RBP_ID_25015819,Human_RBP_ID_26912632 Human_Splice_Rec_1408236,Human_Splice_Rec_1408237,Human_Splice_Rec_1408243,Human_Splice_Rec_1408250,Human_Splice_Rec_1408251,Human_Splice_Rec_1408256,Human_Splice_Rec_1408257,Human_Splice_Rec_1408266,Human_Splice_Rec_1408267 Human_miRNA_ID_2173680,Human_miRNA_ID_2177124,Human_miRNA_ID_2355620 RMVar_hsa_circ_83213,RMVar_hsa_circ_92643,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822,RMVar_hsa_circ_158820,RMVar_hsa_circ_33685 87677 RMVar_ID_87677 Human_SNP_ID_511891626 m1A Human chr12 - 95003691 95003691 95003691 GGTTTTGCTCGGCGCACCCGGGAGGCGGGGCCAGCGAGGCAAGATGGAGTTAGTGCAGGTCCTGA GGTTTTGCTCGGCGCACCCGGGAGGCGGGGCCGGCGAGGCAAGATGGAGTTAGTGCAGGTCCTGA T C NDUFA12 Ensembl:ENSG00000184752 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:95003676..95003700 26863196 MeRIP-seq:(Medium) rs200224620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246889 Human_Splice_Rec_1408223,Human_Splice_Rec_1408239,Human_Splice_Rec_1408245,Human_Splice_Rec_1408253,Human_Splice_Rec_1408259,Human_Splice_Rec_1408263 RMVar_hsa_circ_111874,RMVar_hsa_circ_158822 87678 RMVar_ID_87678 Human_SNP_ID_511891627 m1A Human chr12 - 95003691 95003691 95003691 GGTTTTGCTCGGCGCACCCGGGAGGCGGGGCCAGCGAGGCAAGATGGAGTTAGTGCAGGTCCTGA GGTTTTGCTCGGCGCACCCGGGAGGCGGGGCCCGCGAGGCAAGATGGAGTTAGTGCAGGTCCTGA T G NDUFA12 Ensembl:ENSG00000184752 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:95003676..95003700 26863196 MeRIP-seq:(Medium) rs200224620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246889 Human_Splice_Rec_1408223,Human_Splice_Rec_1408239,Human_Splice_Rec_1408245,Human_Splice_Rec_1408253,Human_Splice_Rec_1408259,Human_Splice_Rec_1408263 RMVar_hsa_circ_111874,RMVar_hsa_circ_158822 87679 RMVar_ID_87679 Human_SNP_ID_511909441 m1A Human chr12 + 95073482 95073482 95073482 ATTGGGGGGCGCTCCGGGAAGAGAGGTTGAAGAAAGCCGACGGGATGTGGGATCGAGATTCACGG ATTGGGGGGCGCTCCGGGAAGAGAGGTTGAAGCAAGCCGACGGGATGTGGGATCGAGATTCACGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:95073431..95073592 26863196 MeRIP-seq:(Medium) rs570032232 Functional Loss SNV dbSNP153 33..33 33 - - - 87680 RMVar_ID_87680 Human_SNP_ID_511909463 m1A Human chr12 - 95073545 95073545 95073545 GCCGAGAAAGAGGTCACGAACTCTGACCCCCCAGAAATACCCAAACACAGAAAGCTCTCTCCGCC GCCGAGAAAGAGGTCACGAACTCTGACCCCCCGGAAATACCCAAACACAGAAAGCTCTCTCCGCC T C NR2C1 Ensembl:ENSG00000120798 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:95073453..95073554 26863410 MeRIP-seq:(Medium) rs915450614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5462253,Human_RBP_ID_12061535 87681 RMVar_ID_87681 Human_SNP_ID_511909481 m1A Human chr12 - 95073559 95073559 95073559 TAGCGCGCCGCCGAGCCGAGAAAGAGGTCACGAACTCTGACCCCCCAGAAATACCCAAACACAGA TAGCGCGCCGCCGAGCCGAGAAAGAGGTCACGTACTCTGACCCCCCAGAAATACCCAAACACAGA T A NR2C1 Ensembl:ENSG00000120798 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:95073462..95073572 26863410 MeRIP-seq:(Medium) rs940488332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5462253,Human_RBP_ID_12061535 87682 RMVar_ID_87682 Human_SNP_ID_511945435 m1A Human chr12 - 95217277 95217277 95217277 GGAACAATGGACTGAAAGGGGAAGATGGATTGAGGGGCCGAGCGGGGAAGCGAGCTGCACCGGGG GGAACAATGGACTGAAAGGGGAAGATGGATTGGGGGGCCGAGCGGGGAAGCGAGCTGCACCGGGG T C FGD6 Ensembl:ENSG00000180263 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:95217185..95217397 26863196 MeRIP-seq:(Medium) rs1478145840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521676 Human_Splice_Rec_1408469,Human_Splice_Rec_1408515,Human_Splice_Rec_1408553,Human_Splice_Rec_1408607 87683 RMVar_ID_87683 Human_SNP_ID_511951554 m1A Human chr12 + 95242166 95242166 95242166 TTTGCTTTTTGTCGTATTCTCTTTCAATAGACATTAAAACTACCACTACTATGGAAGTACCACTA TTTGCTTTTTGTCGTATTCTCTTTCAATAGACGTTAAAACTACCACTACTATGGAAGTACCACTA A G VEZT Ensembl:ENSG00000028203 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:95242164..95242260 26863196 MeRIP-seq:(Medium) rs1047166098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17829341 Human_Splice_Rec_1408642,Human_Splice_Rec_1408710,Human_Splice_Rec_1408711,Human_Splice_Rec_1408818,Human_Splice_Rec_1408819,Human_Splice_Rec_1408856,Human_Splice_Rec_1408857,Human_Splice_Rec_1408958,Human_Splice_Rec_1408959 RMVar_hsa_circ_158868,RMVar_hsa_circ_67368,RMVar_hsa_circ_70131,RMVar_hsa_circ_355152,RMVar_hsa_circ_12442 87684 RMVar_ID_87684 Human_SNP_ID_511965072 m1A Human chr12 + 95300830 95300830 95300830 AGAACCCTGGTTTGAATAACTGATCTGAAATTAGTAGTTACCTGTAAATGGCAGATCTTTTAGGA AGAACCCTGGTTTGAATAACTGATCTGAAATTCGTAGTTACCTGTAAATGGCAGATCTTTTAGGA A C VEZT Ensembl:ENSG00000028203 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4468424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430459,Human_RBP_ID_9023794,Human_RBP_ID_22910132,Human_RBP_ID_23579611,Human_RBP_ID_25012233,Human_RBP_ID_26424107,Human_RBP_ID_26912706 GWAS_ID_10846,GWAS_ID_10847,GWAS_ID_10848,GWAS_ID_10849,GWAS_ID_10850 RMVar_hsa_circ_158889,RMVar_hsa_circ_158880,RMVar_hsa_circ_158890 87685 RMVar_ID_87685 Human_SNP_ID_512009302 m1A Human chr12 + 95474213 95474213 95474213 TGGCGGGTGTGGAGGAGGTAGCGGCCTCCGGGAGCCACCTGAATGGCGACCTGGATCCAGACGAC TGGCGGGTGTGGAGGAGGTAGCGGCCTCCGGGGGCCACCTGAATGGCGACCTGGATCCAGACGAC A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:95474101..95474372;chr12:95474101..95474389;chr12:95474101..95474392 26863196 MeRIP-seq:(Medium) rs1010928319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36483,Human_RBP_ID_430524,Human_RBP_ID_4246892,Human_RBP_ID_9323183,Human_RBP_ID_9365319,Human_RBP_ID_22040664,Human_RBP_ID_24543118,Human_RBP_ID_26320979,Human_RBP_ID_27805827 87686 RMVar_ID_87686 Human_SNP_ID_512009314 m1A Human chr12 + 95474235 95474235 95474235 GGCCTCCGGGAGCCACCTGAATGGCGACCTGGATCCAGACGACAGGGAAGAAGGAGCTGCCTCTA GGCCTCCGGGAGCCACCTGAATGGCGACCTGGGTCCAGACGACAGGGAAGAAGGAGCTGCCTCTA A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:95474126..95483260 32194978 MeRIP-seq:(Medium) rs917601026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36483,Human_RBP_ID_430525,Human_RBP_ID_1479049,Human_RBP_ID_1803397,Human_RBP_ID_2363365,Human_RBP_ID_4246892,Human_RBP_ID_8786115,Human_RBP_ID_9323183,Human_RBP_ID_9365320,Human_RBP_ID_17830477,Human_RBP_ID_22040664,Human_RBP_ID_24543119,Human_RBP_ID_26320980,Human_RBP_ID_27805828 Human_Splice_Rec_1409161,Human_Splice_Rec_1409179,Human_Splice_Rec_1409199,Human_Splice_Rec_1409217,Human_Splice_Rec_1409225,Human_Splice_Rec_1409235,Human_Splice_Rec_1409255,Human_Splice_Rec_1409273 Human_miRNA_ID_975477 87687 RMVar_ID_87687 Human_SNP_ID_512009340 m1A Human chr12 + 95474296 95474296 95474296 TCTACGGCTGAGGAAGCAGCCAAGAAAAAAAGACGAAAGAAGAAGAAGAGCAAAGGGCCTTCTGC TCTACGGCTGAGGAAGCAGCCAAGAAAAAAAGGCGAAAGAAGAAGAAGAGCAAAGGGCCTTCTGC A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:95474101..95476229 26863196 MeRIP-seq:(Medium) rs199912569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36483,Human_RBP_ID_1803398,Human_RBP_ID_2363366,Human_RBP_ID_4260708,Human_RBP_ID_9365320,Human_RBP_ID_17830478,Human_RBP_ID_19058858,Human_RBP_ID_22040664,Human_RBP_ID_24543119,Human_RBP_ID_26320980,Human_RBP_ID_27805828 Human_Splice_Rec_1409161,Human_Splice_Rec_1409179,Human_Splice_Rec_1409199,Human_Splice_Rec_1409217,Human_Splice_Rec_1409225,Human_Splice_Rec_1409235,Human_Splice_Rec_1409255,Human_Splice_Rec_1409273 87688 RMVar_ID_87688 Human_SNP_ID_512009783 m1A Human chr12 + 95476123 95476123 95476123 AAAGAATCAGGAGCCTCAGTGGATGAAGTAGCAAGACAGTTGGAAAGATCAGCATTGGAAGATAA AAAGAATCAGGAGCCTCAGTGGATGAAGTAGCGAGACAGTTGGAAAGATCAGCATTGGAAGATAA A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:95476022..95476222 26863196 MeRIP-seq:(Medium) rs769705278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33866,Human_RBP_ID_1803400,Human_RBP_ID_6235722,Human_RBP_ID_9344656,Human_RBP_ID_12063314,Human_RBP_ID_17474422,Human_RBP_ID_23579674,Human_RBP_ID_24543121,Human_RBP_ID_26321847,Human_RBP_ID_27805830 Human_Splice_Rec_1409162,Human_Splice_Rec_1409163,Human_Splice_Rec_1409180,Human_Splice_Rec_1409181,Human_Splice_Rec_1409200,Human_Splice_Rec_1409201,Human_Splice_Rec_1409218,Human_Splice_Rec_1409219,Human_Splice_Rec_1409227,Human_Splice_Rec_1409236,Human_Splice_Rec_1409237,Human_Splice_Rec_1409274,Human_Splice_Rec_1409275,Human_Splice_Rec_1409293 Human_miRNA_ID_1264508,Human_miRNA_ID_2611401 RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 87689 RMVar_ID_87689 Human_SNP_ID_512009795 m1A Human chr12 + 95476159 95476159 95476159 CAGTTGGAAAGATCAGCATTGGAAGATAAAGAAAGAGATGAAGATGATGAAGGTAAATGGTTAAT CAGTTGGAAAGATCAGCATTGGAAGATAAAGAGAGAGATGAAGATGATGAAGGTAAATGGTTAAT A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:95476001..95476240 26863196 MeRIP-seq:(Medium) rs770452136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194825,Human_RBP_ID_430526,Human_RBP_ID_878387,Human_RBP_ID_1479052,Human_RBP_ID_1803400,Human_RBP_ID_4244793,Human_RBP_ID_6235722,Human_RBP_ID_9344656,Human_RBP_ID_9365322,Human_RBP_ID_18434895,Human_RBP_ID_18635106,Human_RBP_ID_19058859,Human_RBP_ID_23581764,Human_RBP_ID_24543121,Human_RBP_ID_26321848,Human_RBP_ID_27805830 Human_Splice_Rec_1409162,Human_Splice_Rec_1409163,Human_Splice_Rec_1409180,Human_Splice_Rec_1409181,Human_Splice_Rec_1409200,Human_Splice_Rec_1409201,Human_Splice_Rec_1409218,Human_Splice_Rec_1409219,Human_Splice_Rec_1409226,Human_Splice_Rec_1409227,Human_Splice_Rec_1409236,Human_Splice_Rec_1409237,Human_Splice_Rec_1409274,Human_Splice_Rec_1409275,Human_Splice_Rec_1409293 RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 87690 RMVar_ID_87690 Human_SNP_ID_512011518 m1A Human chr12 - 95483204 95483204 95483204 CCATCTCCATCGCCATCTCCATCTAAGAAAAGACATTTCAAGTACATGTTCATTTAAACCTCATA CCATCTCCATCGCCATCTCCATCTAAGAAAAGTCATTTCAAGTACATGTTCATTTAAACCTCATA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:95483201..95483300 26863196 MeRIP-seq:(Medium) rs1416125013 Functional Loss SNV dbSNP153 33..33 33 - - - 87691 RMVar_ID_87691 Human_SNP_ID_512012207 m1A Human chr12 + 95485881 95485881 95485881 AGAAGTTAATGCTTTATTTGTATCTCACAGCAAAAGTTCAAACAGACCCTCCCTCAGTTCCAATA AGAAGTTAATGCTTTATTTGTATCTCACAGCAGAAGTTCAAACAGACCCTCCCTCAGTTCCAATA A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:95485876..95485925;chr12:95485876..95485975 26863196 MeRIP-seq:(Medium) rs200917784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194448,Human_RBP_ID_873208,Human_RBP_ID_1479552,Human_RBP_ID_9365325,Human_RBP_ID_22539330,Human_RBP_ID_23113346,Human_RBP_ID_24543124,Human_RBP_ID_26320981,Human_RBP_ID_27805836 Human_Splice_Rec_1409166,Human_Splice_Rec_1409202,Human_Splice_Rec_1409224,Human_Splice_Rec_1409230,Human_Splice_Rec_1409240,Human_Splice_Rec_1409258,Human_Splice_Rec_1409278,Human_Splice_Rec_1409296 Human_miRNA_ID_2690215,Human_miRNA_ID_2693483 RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_17588,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_158903,RMVar_hsa_circ_358878,RMVar_hsa_circ_32493,RMVar_hsa_circ_351610,RMVar_hsa_circ_284975,RMVar_hsa_circ_314076,RMVar_hsa_circ_268859,RMVar_hsa_circ_158904 87692 RMVar_ID_87692 Human_SNP_ID_512019173 m1A Human chr12 + 95512824 95512824 95512824 ATTTTTCAGGAAGGAGAAGTATATGCAATTGAAACCTTTGGTAGTACAGGAAAAGGTGTTGTTCA ATTTTTCAGGAAGGAGAAGTATATGCAATTGAGACCTTTGGTAGTACAGGAAAAGGTGTTGTTCA A G METAP2 Ensembl:ENSG00000111142 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs934573277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1803450,Human_RBP_ID_3417454,Human_RBP_ID_3942015,Human_RBP_ID_8229766,Human_RBP_ID_9344659,Human_RBP_ID_9365338,Human_RBP_ID_17650202,Human_RBP_ID_17829428,Human_RBP_ID_23579766,Human_RBP_ID_26321862,Human_RBP_ID_26768268,Human_RBP_ID_26912766,Human_RBP_ID_27805848 Human_Splice_Rec_1409176,Human_Splice_Rec_1409177,Human_Splice_Rec_1409196,Human_Splice_Rec_1409197,Human_Splice_Rec_1409214,Human_Splice_Rec_1409215,Human_Splice_Rec_1409252,Human_Splice_Rec_1409253,Human_Splice_Rec_1409270,Human_Splice_Rec_1409271,Human_Splice_Rec_1409290,Human_Splice_Rec_1409291 Human_miRNA_ID_1398913,Human_miRNA_ID_2717497 RMVar_hsa_circ_1938,RMVar_hsa_circ_17588,RMVar_hsa_circ_268859,RMVar_hsa_circ_74069,RMVar_hsa_circ_119507,RMVar_hsa_circ_158907 87693 RMVar_ID_87693 Human_SNP_ID_512078843 m1A Human chr12 - 95752009 95752009 95752009 GAGGACGCAAAGGAAGCTTTGGATTGGGAAGAAGGGCGGCAATGAGATATAGCTGTAGTCCAGGA GAGGACGCAAAGGAAGCTTTGGATTGGGAAGACGGGCGGCAATGAGATATAGCTGTAGTCCAGGA T G NTN4 Ensembl:ENSG00000074527 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:95751969..95752087 26863196 MeRIP-seq:(Medium) rs1317899696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43624,RMVar_hsa_circ_347496,RMVar_hsa_circ_50674,RMVar_hsa_circ_158924,RMVar_hsa_circ_121084,RMVar_hsa_circ_158925 87694 RMVar_ID_87694 Human_SNP_ID_512079149 m1A Human chr12 - 95752894 95752894 95752894 CATCAGGTATGAGGAAGAAAATAGATTTTGGAAGCTATGAGAAATGTAGAGAGTGAGTTGAGCAT CATCAGGTATGAGGAAGAAAATAGATTTTGGATGCTATGAGAAATGTAGAGAGTGAGTTGAGCAT T A NTN4 Ensembl:ENSG00000074527 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:95752891..95753173 26863196 MeRIP-seq:(Medium) rs1565908109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43624,RMVar_hsa_circ_347496,RMVar_hsa_circ_50674,RMVar_hsa_circ_158924,RMVar_hsa_circ_121084,RMVar_hsa_circ_158925 87695 RMVar_ID_87695 Human_SNP_ID_512087689 m1A Human chr12 - 95790633 95790633 95790633 CTCGCAAAGTTCAGCGGCGGCTGCGGGCGCCGAGCCCCGGGCTAGCGGCAGACGAGCCCGCAGGG CTCGCAAAGTTCAGCGGCGGCTGCGGGCGCCGGGCCCCGGGCTAGCGGCAGACGAGCCCGCAGGG T C NTN4 Ensembl:ENSG00000074527 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:95790516..95790690 26863196 MeRIP-seq:(Medium) rs950767448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430615,Human_RBP_ID_4246237 RMVar_hsa_circ_158924,RMVar_hsa_circ_121084,RMVar_hsa_circ_158925 87696 RMVar_ID_87696 Human_SNP_ID_512103204 m1A Human chr12 - 95859070 95859070 95859070 TCTCCCGCCGTTCTCTTTCTCCTTACCATCGTAACCACGGCCGAATGTTGCAGGCTACTCTCTGC TCTCCCGCCGTTCTCTTTCTCCTTACCATCGTGACCACGGCCGAATGTTGCAGGCTACTCTCTGC T C lnc-CCDC38-2 RNACentral:URS00008BE6CD lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:95858951..95859125 26863410 MeRIP-seq:(Medium) rs200504470 Functional Loss SNV dbSNP153 33..33 33 - - - 87697 RMVar_ID_87697 Human_SNP_ID_512139669 m1A Human chr12 + 96005225 96005225 96005225 GGATTCTTTACTGTCAACCCCTATAGCCAGTCAGTCACAGAGCTCTGTGCTTTCACCCTGTGTAA GGATTCTTTACTGTCAACCCCTATAGCCAGTCCGTCACAGAGCTCTGTGCTTTCACCCTGTGTAA A C AC007298.2 Ensembl:ENSG00000257878 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:96005223..96005378 26863196 MeRIP-seq:(Medium) rs1566001438 Functional Loss SNV dbSNP153 33..33 33 - - - 87698 RMVar_ID_87698 Human_SNP_ID_512146367 m1A Human chr12 + 96035509 96035509 96035509 AAGCCGGAGAGGCCAACGAACAGGTATCCACTATCTCGGGCATGGCTCTGGGGGATCACACAGCA AAGCCGGAGAGGCCAACGAACAGGTATCCACTGTCTCGGGCATGGCTCTGGGGGATCACACAGCA A G NONHSAG011990.2 RNACentral:URS00008B3E1C lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:96035459..96035549 26863196 MeRIP-seq:(Medium) rs79510571 Functional Loss SNV dbSNP153 33..33 33 - - - 87699 RMVar_ID_87699 Human_SNP_ID_512146583 m1A Human chr12 - 96036028 96036028 96036028 GCGTGACAGGCGGGGATACTCACCACTATACTAACGAGGAACCGCACGAAAGAAAGCCTTCTGAT GCGTGACAGGCGGGGATACTCACCACTATACTCACGAGGAACCGCACGAAAGAAAGCCTTCTGAT T G LTA4H Ensembl:ENSG00000111144 Protein coding intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1312266693 Functional Loss SNV dbSNP153 33..33 33 - - - 87700 RMVar_ID_87700 Human_SNP_ID_512146640 m1A Human chr12 + 96036077 96036077 96036077 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGCACAGTAATTGTTTTT TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGGCACAGTAATTGTTTTT A G tRNA-Asp-GTC-2-1,NONHSAG011990.2,NONHSAG011990.2:2,AB330774-001,AB330774-001:2,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00008B3E1C,RNACentral:URS00009C253D,RNACentral:URS00000711F0,RNACentral:URS00002B094D,RNACentral:URS00005EA0AD tRNA,lincRNA,lincRNA,misc_RNA,misc_RNA,tRNA exon,intron,intron,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs189963689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430687,Human_RBP_ID_1358935,Human_RBP_ID_1479151,Human_RBP_ID_1803529,Human_RBP_ID_6236623,Human_RBP_ID_8385853,Human_RBP_ID_9023900,Human_RBP_ID_17581824,Human_RBP_ID_17829538,Human_RBP_ID_18434910,Human_RBP_ID_18635225,Human_RBP_ID_19829548,Human_RBP_ID_22795594,Human_RBP_ID_23125981,Human_RBP_ID_23579945,Human_RBP_ID_26616474,Human_RBP_ID_27635285 87701 RMVar_ID_87701 Human_SNP_ID_512200091 m1A Human chr12 + 96247347 96247347 96247347 ACCAGGCCGGTGGTGTCCCTGCCTTCCACGTCAGAGGCTGCGGCGGCGTCCGCCTTCCTGGCCTC ACCAGGCCGGTGGTGTCCCTGCCTTCCACGTCCGAGGCTGCGGCGGCGTCCGCCTTCCTGGCCTC A C ELK3 Ensembl:ENSG00000111145 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:96247296..96247374 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - RMVar_hsa_circ_29031,RMVar_hsa_circ_100665,RMVar_hsa_circ_158936,RMVar_hsa_circ_335593 87702 RMVar_ID_87702 Human_SNP_ID_512200189 m1A Human chr12 + 96247529 96247529 96247529 ACACAGAAGCCTCTTCCTGGAGGCCGCCTGCCATGACTCCGATTCCCTGGAGCCCTTGAACCTGT ACACAGAAGCCTCTTCCTGGAGGCCGCCTGCCGTGACTCCGATTCCCTGGAGCCCTTGAACCTGT A G ELK3 Ensembl:ENSG00000111145 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:96247482..96247571 26863196 MeRIP-seq:(Medium) rs779142846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357702,Human_RBP_ID_18935606 RMVar_hsa_circ_29031,RMVar_hsa_circ_100665,RMVar_hsa_circ_158936,RMVar_hsa_circ_335593 87703 RMVar_ID_87703 Human_SNP_ID_512238761 m1A Human chr12 + 96400375 96400375 96400375 GCGGCTCTGCGGCGGCCCGCGGGGAGCTCAGGAGACTGCGGGCGGCCGCGTTCGCTCCTTGCGTG GCGGCTCTGCGGCGGCCCGCGGGGAGCTCAGGCGACTGCGGGCGGCCGCGTTCGCTCCTTGCGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:96400327..96400520 26863196 MeRIP-seq:(Medium) rs1052645421 Functional Loss SNV dbSNP153 33..33 33 - - - 87704 RMVar_ID_87704 Human_SNP_ID_512261941 m1A Human chr12 + 96489963 96489963 96489963 GCGCTGGCGGGGCACTGGGGAGGGCGCCGGCCAGAGGAGGGACCCCTGGAAAGGGCTGGAGGATG GCGCTGGCGGGGCACTGGGGAGGGCGCCGGCCGGAGGAGGGACCCCTGGAAAGGGCTGGAGGATG A G CFAP54 Ensembl:ENSG00000188596 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:96489958..96490023 26863196 MeRIP-seq:(Medium) rs998213591 Functional Loss SNV dbSNP153 33..33 33 - - - 87705 RMVar_ID_87705 Human_SNP_ID_512755320 m1A Human chr12 - 98503510 98503510 98503510 GCGTGACAGGCGGGGATACTAACCACTATACTAACGAGGAGTCGTTAGGCTGTGTATTTTCTCAG GCGTGACAGGCGGGGATACTAACCACTATACTCACGAGGAGTCGTTAGGCTGTGTATTTTCTCAG T G LINC02453 Ensembl:ENSG00000245017 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1374741912 Functional Loss SNV dbSNP153 33..33 33 - - - 87706 RMVar_ID_87706 Human_SNP_ID_512755321 m1A Human chr12 + 98503511 98503511 98503511 TGAGAAAATACACAGCCTAACGACTCCTCGTTAGTATAGTGGTTAGTATCCCCGCCTGTCACGCG TGAGAAAATACACAGCCTAACGACTCCTCGTTTGTATAGTGGTTAGTATCCCCGCCTGTCACGCG A T tRNA-Asp-GTC-1-1,lnc-TMPO-1 RNACentral:URS000013899F,RNACentral:URS00008BE31F tRNA,lincRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1178588403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269534,Human_RBP_ID_275733,Human_RBP_ID_431398,Human_RBP_ID_995159,Human_RBP_ID_1083337,Human_RBP_ID_1128010,Human_RBP_ID_1168780,Human_RBP_ID_1358966,Human_RBP_ID_1479280,Human_RBP_ID_2364236,Human_RBP_ID_3417928,Human_RBP_ID_4245288,Human_RBP_ID_5094810,Human_RBP_ID_5174132,Human_RBP_ID_5256972,Human_RBP_ID_5274033,Human_RBP_ID_5417509,Human_RBP_ID_5438258,Human_RBP_ID_5462267,Human_RBP_ID_5492273,Human_RBP_ID_5536082,Human_RBP_ID_6238040,Human_RBP_ID_8247913,Human_RBP_ID_8386043,Human_RBP_ID_8786270,Human_RBP_ID_9717126,Human_RBP_ID_12067592,Human_RBP_ID_16993416,Human_RBP_ID_17474515,Human_RBP_ID_17685625,Human_RBP_ID_17829816,Human_RBP_ID_18199346,Human_RBP_ID_18206470,Human_RBP_ID_18265628,Human_RBP_ID_18434916,Human_RBP_ID_18635414,Human_RBP_ID_19030570,Human_RBP_ID_19823112,Human_RBP_ID_22039056,Human_RBP_ID_22178369,Human_RBP_ID_22384559,Human_RBP_ID_22421053,Human_RBP_ID_22494168,Human_RBP_ID_22795605,Human_RBP_ID_23113462,Human_RBP_ID_23125990,Human_RBP_ID_23159402,Human_RBP_ID_23306338,Human_RBP_ID_23581211,Human_RBP_ID_24407823,Human_RBP_ID_24468231,Human_RBP_ID_26420775,Human_RBP_ID_26616608,Human_RBP_ID_26748125,Human_RBP_ID_26912879,Human_RBP_ID_27155044,Human_RBP_ID_27219222,Human_RBP_ID_27425687,Human_RBP_ID_27558377,Human_RBP_ID_27635442 87707 RMVar_ID_87707 Human_SNP_ID_512755797 m1A Human chr12 + 98504308 98504308 98504308 GTCTGACTCCAGATCAGAAGGCTGCGTGTTCGAATCACGTCGGGGTCAAACTTTTTTTTTTTCCT GTCTGACTCCAGATCAGAAGGCTGCGTGTTCGGATCACGTCGGGGTCAAACTTTTTTTTTTTCCT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1257079753 Functional Loss SNV dbSNP153 33..33 33 - - - 87708 RMVar_ID_87708 Human_SNP_ID_512755798 m1A Human chr12 + 98504308 98504308 98504308 GTCTGACTCCAGATCAGAAGGCTGCGTGTTCGAATCACGTCGGGGTCAAACTTTTTTTTTTTCCT GTCTGACTCCAGATCAGAAGGCTGCGTGTTCGTATCACGTCGGGGTCAAACTTTTTTTTTTTCCT A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1257079753 Functional Loss SNV dbSNP153 33..33 33 - - - 87709 RMVar_ID_87709 Human_SNP_ID_512759049 m1A Human chr12 + 98515935 98515935 98515935 AAAAGACAAGTTGAAGAGTGAGTTGGTCGCCAACAATGTGACGCTGCCGGCCGGGGAGCAGCGCA AAAAGACAAGTTGAAGAGTGAGTTGGTCGCCAGCAATGTGACGCTGCCGGCCGGGGAGCAGCGCA A G TMPO Ensembl:ENSG00000120802 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:98515884..98516126 32194978 MeRIP-seq:(Medium) rs1555201560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1479297,Human_RBP_ID_4245367,Human_RBP_ID_6238086,Human_RBP_ID_8386058,Human_RBP_ID_8786285,Human_RBP_ID_9322655,Human_RBP_ID_12067617,Human_RBP_ID_18635430,Human_RBP_ID_22039490,Human_RBP_ID_22494173,Human_RBP_ID_23581229,Human_RBP_ID_26424120 Human_miRNA_ID_216193,Human_miRNA_ID_660487,Human_miRNA_ID_666677,Human_miRNA_ID_672295,Human_miRNA_ID_2022246,Human_miRNA_ID_2260788,Human_miRNA_ID_2263833,Human_miRNA_ID_2266902 RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 87710 RMVar_ID_87710 Human_SNP_ID_512759111 m1A Human chr12 + 98516045 98516045 98516045 ACCGGCCGCCGCTCCCCGCCGGCACCAACAGCAAGGGGCCCCCGGACTTCTCCAGTGACGAAGAG ACCGGCCGCCGCTCCCCGCCGGCACCAACAGCGAGGGGCCCCCGGACTTCTCCAGTGACGAAGAG A G TMPO Ensembl:ENSG00000120802 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:98515637..98516126 32194978 MeRIP-seq:(Medium) rs758451979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_995168,Human_RBP_ID_3417946,Human_RBP_ID_4245376,Human_RBP_ID_6238090,Human_RBP_ID_8386060,Human_RBP_ID_8786287,Human_RBP_ID_9323190,Human_RBP_ID_27219241,Human_RBP_ID_27425702 Human_miRNA_ID_2295712 RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 87711 RMVar_ID_87711 Human_SNP_ID_512769006 m1A Human chr12 + 98549000 98549000 98549000 AAAATTAGCTGGGCGTGATGATGTGCGCCTGTAGTCCTGTCTACTAGGGAGACTGAGGCAGGAGA AAAATTAGCTGGGCGTGATGATGTGCGCCTGTGGTCCTGTCTACTAGGGAGACTGAGGCAGGAGA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:98548926..98549075 32194978 MeRIP-seq:(Medium) rs562809468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431041,Human_RBP_ID_2364452,Human_RBP_ID_6238668,Human_RBP_ID_8179350,Human_RBP_ID_12068721,Human_RBP_ID_18265703,Human_RBP_ID_23306187,Human_RBP_ID_23581369,Human_RBP_ID_24365864,Human_RBP_ID_26420847 87712 RMVar_ID_87712 Human_SNP_ID_512769017 m1A Human chr12 + 98549041 98549041 98549041 TACTAGGGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGA TACTAGGGAGACTGAGGCAGGAGAATCGTTTGGACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1380312362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25014605,Human_RBP_ID_26421546,Human_RBP_ID_27425735 87713 RMVar_ID_87713 Human_SNP_ID_512769036 m1A Human chr12 + 98549107 98549107 98549107 TACGTCACTGCACTGTAGCCTGGCGACAGAGCAAGACTCCATCTCAAAAAAAATAAAAAAGTACA TACGTCACTGCACTGTAGCCTGGCGACAGAGCGAGACTCCATCTCAAAAAAAATAAAAAAGTACA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs968204668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159472,Human_RBP_ID_26420849 87714 RMVar_ID_87714 Human_SNP_ID_512769100 m1A Human chr12 + 98549318 98549318 98549318 ACGATCTGGGCTCGATGCAACCTCTGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCGGCAGAGAC ACGATCTGGGCTCGATGCAACCTCTGCCTCCCGGGTTCAAGCAATTTTCCTGCCTCGGCAGAGAC A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1174498646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6238679,Human_RBP_ID_17561240 87715 RMVar_ID_87715 Human_SNP_ID_512769134 m1A Human chr12 + 98549423 98549423 98549423 ACCTCAAGTGATCAGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGATCCACTGCAC ACCTCAAGTGATCAGCCCACCTCAGCTTCCCAGAGTGCTGGGATTACAGGTGTGATCCACTGCAC A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3177180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431043,Human_RBP_ID_4245530,Human_RBP_ID_23159478,Human_RBP_ID_26421547 Human_miRNA_ID_1143786 87716 RMVar_ID_87716 Human_SNP_ID_512780462 m1A Human chr12 + 98593700 98593700 98593700 ACCCGGAGGACGTCCGGCCTCTGTGAGCCGCAACCTTTCCAAGGGAGTGGTTGTGTGATCGCCAT ACCCGGAGGACGTCCGGCCTCTGTGAGCCGCAGCCTTTCCAAGGGAGTGGTTGTGTGATCGCCAT A G SLC25A3 Ensembl:ENSG00000075415 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:98593676..98593700 26863196 MeRIP-seq:(Medium) rs1220025039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431088,Human_RBP_ID_4246241,Human_RBP_ID_8386199,Human_RBP_ID_17241951,Human_RBP_ID_18417668,Human_RBP_ID_22039495,Human_RBP_ID_22437368,Human_RBP_ID_22756085,Human_RBP_ID_23581402,Human_RBP_ID_26420883,Human_RBP_ID_26912966,Human_RBP_ID_27219311,Human_RBP_ID_27425740 Human_Splice_Rec_1411499,Human_Splice_Rec_1411525,Human_Splice_Rec_1411539,Human_Splice_Rec_1411553,Human_Splice_Rec_1411565,Human_Splice_Rec_1411571,Human_Splice_Rec_1411577,Human_Splice_Rec_1411583,Human_Splice_Rec_1411597,Human_Splice_Rec_1411611 87717 RMVar_ID_87717 Human_SNP_ID_512780647 m1A Human chr12 - 98594115 98594115 98594115 GTCTGATCTCACCTTCCACGGCGGCGGCTGCCAGGTTGCGAGGGCGGCGGGGCTGGCCCGTGGGC GTCTGATCTCACCTTCCACGGCGGCGGCTGCCCGGTTGCGAGGGCGGCGGGGCTGGCCCGTGGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:98593947..98594191;chr12:98593949..98594167 26863196 MeRIP-seq:(Medium) rs1220709884 Functional Loss SNV dbSNP153 33..33 33 - - - 87718 RMVar_ID_87718 Human_SNP_ID_512781167 m1A Human chr12 + 98595740 98595740 98595740 GTGTCTTCTCTTACTACAGAGTACAGTTGTGAATTTGGCTCCGCGAAGTATTATGCACTGTGTGG GTGTCTTCTCTTACTACAGAGTACAGTTGTGAGTTTGGCTCCGCGAAGTATTATGCACTGTGTGG A G SLC25A3 Ensembl:ENSG00000075415 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:98595726..98595750 26863196 MeRIP-seq:(Medium) rs761707071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431103,Human_RBP_ID_752968,Human_RBP_ID_995289,Human_RBP_ID_1168835,Human_RBP_ID_1271213,Human_RBP_ID_1359000,Human_RBP_ID_1803910,Human_RBP_ID_4260961,Human_RBP_ID_17600510,Human_RBP_ID_17650465,Human_RBP_ID_17685648,Human_RBP_ID_18635526,Human_RBP_ID_19058890,Human_RBP_ID_22437971,Human_RBP_ID_22646790,Human_RBP_ID_22756086,Human_RBP_ID_23207786,Human_RBP_ID_23581427,Human_RBP_ID_25014694,Human_RBP_ID_27219318 Human_Splice_Rec_1411502,Human_Splice_Rec_1411514,Human_Splice_Rec_1411580,Human_Splice_Rec_1411586,Human_Splice_Rec_1411600,Human_Splice_Rec_1411626 RMVar_hsa_circ_117595,RMVar_hsa_circ_45544,RMVar_hsa_circ_378784,RMVar_hsa_circ_159021,RMVar_hsa_circ_282329,RMVar_hsa_circ_362528,RMVar_hsa_circ_159020,RMVar_hsa_circ_284772,RMVar_hsa_circ_159022 87719 RMVar_ID_87719 Human_SNP_ID_512781168 m1A Human chr12 + 98595740 98595740 98595740 GTGTCTTCTCTTACTACAGAGTACAGTTGTGAATTTGGCTCCGCGAAGTATTATGCACTGTGTGG GTGTCTTCTCTTACTACAGAGTACAGTTGTGATTTTGGCTCCGCGAAGTATTATGCACTGTGTGG A T SLC25A3 Ensembl:ENSG00000075415 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:98595726..98595750 26863196 MeRIP-seq:(Medium) rs761707071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431103,Human_RBP_ID_752968,Human_RBP_ID_995289,Human_RBP_ID_1168835,Human_RBP_ID_1271213,Human_RBP_ID_1359000,Human_RBP_ID_1803910,Human_RBP_ID_4260961,Human_RBP_ID_17600510,Human_RBP_ID_17650465,Human_RBP_ID_17685648,Human_RBP_ID_18635526,Human_RBP_ID_19058890,Human_RBP_ID_22437971,Human_RBP_ID_22646790,Human_RBP_ID_22756086,Human_RBP_ID_23207786,Human_RBP_ID_23581427,Human_RBP_ID_25014694,Human_RBP_ID_27219318 Human_Splice_Rec_1411502,Human_Splice_Rec_1411514,Human_Splice_Rec_1411580,Human_Splice_Rec_1411586,Human_Splice_Rec_1411600,Human_Splice_Rec_1411626 RMVar_hsa_circ_117595,RMVar_hsa_circ_45544,RMVar_hsa_circ_378784,RMVar_hsa_circ_159021,RMVar_hsa_circ_282329,RMVar_hsa_circ_362528,RMVar_hsa_circ_159020,RMVar_hsa_circ_284772,RMVar_hsa_circ_159022 87720 RMVar_ID_87720 Human_SNP_ID_512781489 m1A Human chr12 + 98596874 98596874 98596874 GAAACCTCATCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTGGCGTGCCTGTAGTCGCAGC GAAACCTCATCTCTGCTAAAAATACAAAAATTGGCTGGGCATGGTGGCGTGCCTGTAGTCGCAGC A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs927656465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45544,RMVar_hsa_circ_378784,RMVar_hsa_circ_362528,RMVar_hsa_circ_284772,RMVar_hsa_circ_159022 87721 RMVar_ID_87721 Human_SNP_ID_512781799 m1A Human chr12 - 98597991 98597991 98597991 ATTGCTATACAAGACTTTAAAGACTTCATAAAAGCCAAACTTGCAGAGTCCCTGCATGGAGTAGC ATTGCTATACAAGACTTTAAAGACTTCATAAAGGCCAAACTTGCAGAGTCCCTGCATGGAGTAGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:98597851..98598050 32194978 MeRIP-seq:(Medium) rs11544643 Functional Loss SNV dbSNP153 33..33 33 - - - 87722 RMVar_ID_87722 Human_SNP_ID_512782472 m1A Human chr12 + 98600078 98600078 98600078 TACAAGTTTGTGGTTCCTAAGCCCCGCAGTGAATGTTCAAAGCCAGAGCAGCTGGTTGTAACATT TACAAGTTTGTGGTTCCTAAGCCCCGCAGTGATTGTTCAAAGCCAGAGCAGCTGGTTGTAACATT A T SLC25A3 Ensembl:ENSG00000075415 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:98600028..98600170 26863196 MeRIP-seq:(Medium) rs778247220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431119,Human_RBP_ID_995296,Human_RBP_ID_4260987,Human_RBP_ID_8386240,Human_RBP_ID_9279177,Human_RBP_ID_17241953,Human_RBP_ID_21885432,Human_RBP_ID_22436083,Human_RBP_ID_22756093,Human_RBP_ID_23207790,Human_RBP_ID_23581452,Human_RBP_ID_27219331 Human_Splice_Rec_1411509,Human_Splice_Rec_1411521,Human_Splice_Rec_1411535,Human_Splice_Rec_1411549,Human_Splice_Rec_1411561,Human_Splice_Rec_1411593,Human_Splice_Rec_1411607,Human_Splice_Rec_1411621,Human_Splice_Rec_1411633,Human_Splice_Rec_1411639 Human_miRNA_ID_793397,Human_miRNA_ID_2120036,Human_miRNA_ID_2123253,Human_miRNA_ID_2126471,Human_miRNA_ID_2129692,Human_miRNA_ID_2602316,Human_miRNA_ID_2879833,Human_miRNA_ID_2907865,Human_miRNA_ID_3026703 RMVar_hsa_circ_121482,RMVar_hsa_circ_45544,RMVar_hsa_circ_362528,RMVar_hsa_circ_299969,RMVar_hsa_circ_337988,RMVar_hsa_circ_159024 87723 RMVar_ID_87723 Human_SNP_ID_512786554 m1A Human chr12 + 98614340 98614340 98614340 CAATTGTTCCATGATAGCTTCAGATTTCTGCCACTATAAGAAAATATAATATCACAATGATTAAA CAATTGTTCCATGATAGCTTCAGATTTCTGCCGCTATAAGAAAATATAATATCACAATGATTAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:98614296..98624304 32194978 MeRIP-seq:(Medium) rs975433793 Functional Loss SNV dbSNP153 33..33 33 - - - 87724 RMVar_ID_87724 Human_SNP_ID_512789261 m1A Human chr12 - 98625652 98625652 98625652 TAATATTTTTAATGTTTTTTAAAGCATTAATGAACATCATCATTAATTTCACCTATTATATTGTA TAATATTTTTAATGTTTTTTAAAGCATTAATGGACATCATCATTAATTTCACCTATTATATTGTA T C IKBIP Ensembl:ENSG00000166130 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7962649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8070277,Human_RBP_ID_17356823,Human_RBP_ID_17474611,Human_RBP_ID_17830059,Human_RBP_ID_22384126,Human_RBP_ID_27635655 Human_miRNA_ID_359098 GWAS_ID_10851,GWAS_ID_10852,GWAS_ID_10853,GWAS_ID_10854,GWAS_ID_10855,GWAS_ID_10856,GWAS_ID_10857,GWAS_ID_10858,GWAS_ID_10859,GWAS_ID_10860,GWAS_ID_10861 RMVar_hsa_circ_90534,RMVar_hsa_circ_159025,RMVar_hsa_circ_159026 87725 RMVar_ID_87725 Human_SNP_ID_512794147 m1A Human chr12 + 98644539 98644539 98644539 CCTCGCGTCCACTTACCAGGCCAGGCCCAGGCACGTCCCCAGCGACAGCAGGCTCAGGCACGTTC CCTCGCGTCCACTTACCAGGCCAGGCCCAGGCCCGTCCCCAGCGACAGCAGGCTCAGGCACGTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr12:98644526..98644750;chr12:98644526..98644725 26863196,32194978 MeRIP-seq:(Medium) rs1404330090 Functional Loss SNV dbSNP153 33..33 33 - - - 87726 RMVar_ID_87726 Human_SNP_ID_512794194 m1A Human chr12 - 98644617 98644617 98644617 CGGAGCCCGGGAAGCGGAGCGAGGGCGGGAAGACCCCCGTGGCCCGGAGCAGCGGAGGCGGGGGC CGGAGCCCGGGAAGCGGAGCGAGGGCGGGAAGGCCCCCGTGGCCCGGAGCAGCGGAGGCGGGGGC T C IKBIP Ensembl:ENSG00000166130 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:98644523..98644725 26863410 MeRIP-seq:(Medium) rs752637333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246242,Human_RBP_ID_18417493,Human_RBP_ID_22436656,Human_RBP_ID_22911024,Human_RBP_ID_26321868 Human_Splice_Rec_1411645,Human_Splice_Rec_1411647,Human_Splice_Rec_1411651 87727 RMVar_ID_87727 Human_SNP_ID_512794489 m1A Human chr12 + 98645342 98645342 98645342 AGCGAGTGGACGTGACTGCTCTATCCCGGGCAAAAGGGATAGAACCAGAGGTGGGGAGTCTGGGC AGCGAGTGGACGTGACTGCTCTATCCCGGGCAGAAGGGATAGAACCAGAGGTGGGGAGTCTGGGC A G APAF1 Ensembl:ENSG00000120868 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:98645296..98645441;chr12:98645190..98645462 26863196 MeRIP-seq:(Medium) rs1400657014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872523,Human_RBP_ID_26323257,Human_RBP_ID_27805858 RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 87728 RMVar_ID_87728 Human_SNP_ID_512794518 m1A Human chr12 - 98645432 98645432 98645432 CCTTCCCCCGACGGCGGCTGCACCCCGGAGGGAGCCCGGCGCTACTCCGGATGCCGCTGCGGCAC CCTTCCCCCGACGGCGGCTGCACCCCGGAGGGTGCCCGGCGCTACTCCGGATGCCGCTGCGGCAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:98645389..98645489 32194978 MeRIP-seq:(Medium) rs1370778809 Functional Loss SNV dbSNP153 33..33 33 - - - 87729 RMVar_ID_87729 Human_SNP_ID_512794614 m1A Human chr12 - 98645760 98645760 98645760 CGGGACAAGACTGGGAGACTCCAGGCCGGTGGAGGGAAACGGCAACAGGAGTTTTCCACCGGGAA CGGGACAAGACTGGGAGACTCCAGGCCGGTGGCGGGAAACGGCAACAGGAGTTTTCCACCGGGAA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:98645588..98645787 32194978 MeRIP-seq:(Medium) rs1421370847 Functional Loss SNV dbSNP153 33..33 33 - - - 87730 RMVar_ID_87730 Human_SNP_ID_446697133 m1A Human chr10 - 109877862 109877862 109877862 ACTCTGCTTTCTGTCTTTCTGTTACAGGCAACAGGCAGACTTTGTGGACCTGAGCTTCCCAACAA ACTCTGCTTTCTGTCTTTCTGTTACAGGCAACCGGCAGACTTTGTGGACCTGAGCTTCCCAACAA T G XPNPEP1 Ensembl:ENSG00000108039 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:109877759..109878041 32194978 MeRIP-seq:(Medium) rs1455141283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11253946,Human_RBP_ID_18971261 Human_Splice_Rec_1174738,Human_Splice_Rec_1174772,Human_Splice_Rec_1174773,Human_Splice_Rec_1174812,Human_Splice_Rec_1174813,Human_Splice_Rec_1174852,Human_Splice_Rec_1174853,Human_Splice_Rec_1174886,Human_Splice_Rec_1174887,Human_Splice_Rec_1174898,Human_Splice_Rec_1174899,Human_Splice_Rec_1174914,Human_Splice_Rec_1174915,Human_Splice_Rec_1174926,Human_Splice_Rec_1174928,Human_Splice_Rec_1174936 RMVar_hsa_circ_105796,RMVar_hsa_circ_126279,RMVar_hsa_circ_146317,RMVar_hsa_circ_91698,RMVar_hsa_circ_95502,RMVar_hsa_circ_146315,RMVar_hsa_circ_146316,RMVar_hsa_circ_146314,RMVar_hsa_circ_88695,RMVar_hsa_circ_92522,RMVar_hsa_circ_146321,RMVar_hsa_circ_77047,RMVar_hsa_circ_146323,RMVar_hsa_circ_105539,RMVar_hsa_circ_338215,RMVar_hsa_circ_146324,RMVar_hsa_circ_146325 87731 RMVar_ID_87731 Human_SNP_ID_446703526 m1A Human chr10 - 109904261 109904261 109904261 TCAAGCTGGAATCGGGGTGGTGGCATGTGAGGAAGCCATGAGGCTGGGTGCATAACTGTTAGATC TCAAGCTGGAATCGGGGTGGTGGCATGTGAGGGAGCCATGAGGCTGGGTGCATAACTGTTAGATC T C XPNPEP1 Ensembl:ENSG00000108039 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:109904259..109904327 26863196 MeRIP-seq:(Medium) rs1017657978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328100,RMVar_hsa_circ_333206 87732 RMVar_ID_87732 Human_SNP_ID_446704321 m1A Human chr10 + 109907790 109907790 109907790 ATGGCTTGTCTCAGCTGCCGAAGCAGCTCTGAAGTCACCTTTGGAGGCATTCTGCCGTCTGCAAC ATGGCTTGTCTCAGCTGCCGAAGCAGCTCTGACGTCACCTTTGGAGGCATTCTGCCGTCTGCAAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:109907740..109915131 32194978 MeRIP-seq:(Medium) rs1216897206 Functional Loss SNV dbSNP153 33..33 33 - - - 87733 RMVar_ID_87733 Human_SNP_ID_446761337 m1A Human chr10 + 110134766 110134766 110134766 ATTTCTAAAATTCTGCTTCTCTGCCAAAAGCAATGTCTTTCTTGGTTGATATTTGAGTTTTAAAA ATTTCTAAAATTCTGCTTCTCTGCCAAAAGCAGTGTCTTTCTTGGTTGATATTTGAGTTTTAAAA A G ADD3 Ensembl:ENSG00000148700 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:110134716..110134797 32194978 MeRIP-seq:(Medium) rs1554848231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_369569,Human_RBP_ID_8325466 RMVar_hsa_circ_146350 87734 RMVar_ID_87734 Human_SNP_ID_446779820 m1A Human chr10 - 110207885 110207862 110207885 CCGGGGGCTGGGGCGCGGCCACGGCGGGGGGCACAGCCGGGGGCGCGGCGGGGGCCAGCCCCGCG CCGGGGGCTGGGGCGCGGCCACGGCGGGGGGC_______________________CAGCCCCGCG GGCCCCCGCCGCGCCCCCGGCTGT G AL360182.2 Ensembl:ENSG00000228417 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:110207835..110210248 32194978 MeRIP-seq:(Medium) rs1343762554 Functional Loss DEL dbSNP153 33..55 33 - - - Human_RBP_ID_3365530 87735 RMVar_ID_87735 Human_SNP_ID_446779832 m1A Human chr10 - 110207885 110207885 110207885 CCGGGGGCTGGGGCGCGGCCACGGCGGGGGGCACAGCCGGGGGCGCGGCGGGGGCCAGCCCCGCG CCGGGGGCTGGGGCGCGGCCACGGCGGGGGGCTCAGCCGGGGGCGCGGCGGGGGCCAGCCCCGCG T A AL360182.2 Ensembl:ENSG00000228417 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:110207835..110210248 32194978 MeRIP-seq:(Medium) rs770494068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3365530 87736 RMVar_ID_87736 Human_SNP_ID_446779928 m1A Human chr10 - 110208084 110208078 110208084 GGCGCCGAGGAAGAGCAGGGGCCCCCAAACTTACTTTTGTTTTCTTTCTCGATCTGCTCCAGGTA GGCGCCGAGGAAGAGCAGGGGCCCCCAAACTT______GTTTTCTTTCTCGATCTGCTCCAGGTA CAAAAGT C AL360182.2 Ensembl:ENSG00000228417 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:110207896..110210298 26863410 MeRIP-seq:(Medium) rs1231021310 Functional Loss DEL dbSNP153 33..38 33 - - - 87737 RMVar_ID_87737 Human_SNP_ID_446784560 m1A Human chr10 + 110226114 110226114 110226114 CGCGGCCGAGCTGGCCCGCCCGCCCGTCGCACATGTTCCGGAACGGCGCCCGGCCGTAGCCGCCT CGCGGCCGAGCTGGCCCGCCCGCCCGTCGCACGTGTTCCGGAACGGCGCCCGGCCGTAGCCGCCT A G MXI1 Ensembl:ENSG00000119950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:110226066..110226240 26863196 MeRIP-seq:(Medium) rs1449181529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4138757 87738 RMVar_ID_87738 Human_SNP_ID_446784622 m1A Human chr10 + 110226278 110226278 110226278 GCTGGAGGCTGCCGAGTTTTTGGAGCGCCGGGAGCGAGGTAATGGCTGGGCGCCGCTGCGTGAGC GCTGGAGGCTGCCGAGTTTTTGGAGCGCCGGGGGCGAGGTAATGGCTGGGCGCCGCTGCGTGAGC A G MXI1 Ensembl:ENSG00000119950 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:110226271..110227607 26863196 MeRIP-seq:(Medium) rs1267516098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1175357,Human_Splice_Rec_1175367,Human_Splice_Rec_1175377,Human_Splice_Rec_1175395 87739 RMVar_ID_87739 Human_SNP_ID_446803170 m1A Human chr10 + 110304398 110304398 110304398 GCTGCTCTCCTCCCCGCCACGCAGCACCTCAAAGCCCGCCACAACTCGATCATTCGGACGTGGAA GCTGCTCTCCTCCCCGCCACGCAGCACCTCAACGCCCGCCACAACTCGATCATTCGGACGTGGAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110304395..110304488 26863196 MeRIP-seq:(Medium) rs1432752330 Functional Loss SNV dbSNP153 33..33 33 - - - 87740 RMVar_ID_87740 Human_SNP_ID_446852917 m1A Human chr10 - 110498261 110498261 110498261 CGCCCCGGGCCCGCCGCAGCACCACCGAGTTGAGGTTGACGTTGAGCGAGCCGCGCACGTTCGAG CGCCCCGGGCCCGCCGCAGCACCACCGAGTTGGGGTTGACGTTGAGCGAGCCGCGCACGTTCGAG T C lnc-SMNDC1-3,lnc-SMNDC1-3:2 RNACentral:URS00009B9FBF,RNACentral:URS00008C1384 lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:110497936..110498434 26863196 MeRIP-seq:(Medium) rs867741891 Functional Loss SNV dbSNP153 33..33 33 - - - 87741 RMVar_ID_87741 Human_SNP_ID_446853073 m1A Human chr10 - 110498549 110498525 110498550 GGTGTAGGAGGGCGCCCCGGCGCAGGGAGGGGACCCGGGGGCGCCGGAGGGGCGAGCGTGGCAGG GGTGTAGGAGGGCGCCCCGGCGCAGGGAGGG_________________________CGTGGCAGG GCTCGCCCCTCCGGCGCCCCCGGGTC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:110498506..110498635 26863196 MeRIP-seq:(Medium) rs1224543042 Functional Loss DEL dbSNP153 32..56 33 - - - 87742 RMVar_ID_87742 Human_SNP_ID_446874530 m1A Human chr10 + 110583380 110583380 110583380 TAATTGCCTTATTTTCTGTTTAATACTTTTGAATAGGATATCGAACGCCAAGTTAGAGAATTGAA TAATTGCCTTATTTTCTGTTTAATACTTTTGAGTAGGATATCGAACGCCAAGTTAGAGAATTGAA A G SMC3 Ensembl:ENSG00000108055 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110583376..110583400 26863196 MeRIP-seq:(Medium) rs1331233382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9343653,Human_RBP_ID_11256125,Human_RBP_ID_24779478 RMVar_hsa_circ_6803,RMVar_hsa_circ_95002,RMVar_hsa_circ_123412,RMVar_hsa_circ_146358,RMVar_hsa_circ_87640,RMVar_hsa_circ_109538,RMVar_hsa_circ_312563,RMVar_hsa_circ_377570,RMVar_hsa_circ_146361,RMVar_hsa_circ_364824,RMVar_hsa_circ_146362,RMVar_hsa_circ_90844,RMVar_hsa_circ_146363,RMVar_hsa_circ_146364,RMVar_hsa_circ_146365,RMVar_hsa_circ_64678 87743 RMVar_ID_87743 Human_SNP_ID_446874544 m1A Human chr10 - 110583476 110583476 110583476 TTGGCTTTAAGCTCCAACTTAGTCCTCTGCTTAATCTGCTCTTGTCTTTCAGCACTAAGCTGTTC TTGGCTTTAAGCTCCAACTTAGTCCTCTGCTTTATCTGCTCTTGTCTTTCAGCACTAAGCTGTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110583426..110583475 26863196 MeRIP-seq:(Medium) rs967227703 Functional Loss SNV dbSNP153 33..33 33 - - - 87744 RMVar_ID_87744 Human_SNP_ID_446933156 m1A Human chr10 + 110821276 110821276 110821276 CCTCTGACCTCCATTCTGCATTTTTGTACAGGAACAAGATTGGGAGAGTGAAAGTGAGGCAGAGG CCTCTGACCTCCATTCTGCATTTTTGTACAGGGACAAGATTGGGAGAGTGAAAGTGAGGCAGAGG A G RBM20 Ensembl:ENSG00000203867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:110812736..110821444 26863196 MeRIP-seq:(Medium) rs1208328652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26316709 Human_Splice_Rec_1175854 87745 RMVar_ID_87745 Human_SNP_ID_446933196 m1A Human chr10 + 110821380 110821380 110821380 CAGTGGACGAGGTTGGGGAAGAAGAAGATTTTATCGTGGAACCAGACATCCCAGAGCTGGAAGAA CAGTGGACGAGGTTGGGGAAGAAGAAGATTTTGTCGTGGAACCAGACATCCCAGAGCTGGAAGAA A G RBM20 Ensembl:ENSG00000203867 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110821330..110821416 26863196 MeRIP-seq:(Medium) rs397516608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4106744,Human_RBP_ID_5925267,Human_RBP_ID_22029552,Human_RBP_ID_26316709,Human_RBP_ID_26874598,Human_RBP_ID_27803021 Clinvar_Rec_486,Clinvar_Rec_487 87746 RMVar_ID_87746 Human_SNP_ID_446933197 m1A Human chr10 + 110821380 110821380 110821380 CAGTGGACGAGGTTGGGGAAGAAGAAGATTTTATCGTGGAACCAGACATCCCAGAGCTGGAAGAA CAGTGGACGAGGTTGGGGAAGAAGAAGATTTTTTCGTGGAACCAGACATCCCAGAGCTGGAAGAA A T RBM20 Ensembl:ENSG00000203867 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110821330..110821416 26863196 MeRIP-seq:(Medium) rs397516608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4106744,Human_RBP_ID_5925267,Human_RBP_ID_22029552,Human_RBP_ID_26316709,Human_RBP_ID_26874598,Human_RBP_ID_27803021 Clinvar_Rec_486,Clinvar_Rec_487 87747 RMVar_ID_87747 Human_SNP_ID_446945608 m1A Human chr10 - 110872020 110872020 110872020 CCCGAGCGTGTGAGCCGCGCCTACTGGTACTGACCCCTCGGGCCCCCGCCGCTGCTCGCCCAGGT CCCGAGCGTGTGAGCCGCGCCTACTGGTACTGCCCCCTCGGGCCCCCGCCGCTGCTCGCCCAGGT T G PDCD4-AS1 Ensembl:ENSG00000203497 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr10:110871951..110872069;chr10:110871926..110872060 26863410 MeRIP-seq:(Medium) rs906557494 Functional Loss SNV dbSNP153 33..33 33 - - - 87748 RMVar_ID_87748 Human_SNP_ID_446946780 m1A Human chr10 + 110876016 110876016 110876016 CATTAGGTAATTTGTTTAATCAGTGCAAGCGAAATTAAGGGAAAATGGATGTAGAAAATGAGCAG CATTAGGTAATTTGTTTAATCAGTGCAAGCGAGATTAAGGGAAAATGGATGTAGAAAATGAGCAG A G PDCD4 Ensembl:ENSG00000150593 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:110875922..110876075 26863196 MeRIP-seq:(Medium) rs1439650120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28881,Human_RBP_ID_981431,Human_RBP_ID_1441429,Human_RBP_ID_1760063,Human_RBP_ID_3338356,Human_RBP_ID_4106822,Human_RBP_ID_5925380,Human_RBP_ID_8325735,Human_RBP_ID_8982524,Human_RBP_ID_11257773,Human_RBP_ID_18586748,Human_RBP_ID_23433722,Human_RBP_ID_27602661 Human_Splice_Rec_1175872,Human_Splice_Rec_1175873,Human_Splice_Rec_1175904,Human_Splice_Rec_1175905,Human_Splice_Rec_1175914,Human_Splice_Rec_1175915,Human_Splice_Rec_1175936,Human_Splice_Rec_1175937 RMVar_hsa_circ_287709,RMVar_hsa_circ_357041,RMVar_hsa_circ_367553,RMVar_hsa_circ_362745,RMVar_hsa_circ_355786,RMVar_hsa_circ_62268,RMVar_hsa_circ_72100 87749 RMVar_ID_87749 Human_SNP_ID_446948148 m1A Human chr10 + 110881330 110881330 110881330 AAGAATGAAATAAATGGAAATTGGATTTCAGCATCCTCCATTAACGAAGCTAGAATTAATGCCAA AAGAATGAAATAAATGGAAATTGGATTTCAGCCTCCTCCATTAACGAAGCTAGAATTAATGCCAA A C PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110881181..110883100 26863196 MeRIP-seq:(Medium) rs780026914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28884,Human_RBP_ID_1441438,Human_RBP_ID_1760071,Human_RBP_ID_5925419,Human_RBP_ID_8325741,Human_RBP_ID_27602662 Human_Splice_Rec_1175876,Human_Splice_Rec_1175896,Human_Splice_Rec_1175908,Human_Splice_Rec_1175916,Human_Splice_Rec_1175938,Human_Splice_Rec_1175946 RMVar_hsa_circ_146377,RMVar_hsa_circ_305214,RMVar_hsa_circ_287709,RMVar_hsa_circ_357041,RMVar_hsa_circ_367553,RMVar_hsa_circ_362745,RMVar_hsa_circ_355786,RMVar_hsa_circ_62268,RMVar_hsa_circ_72100,RMVar_hsa_circ_353845,RMVar_hsa_circ_354630,RMVar_hsa_circ_348239,RMVar_hsa_circ_64240,RMVar_hsa_circ_273239,RMVar_hsa_circ_146378,RMVar_hsa_circ_146379,RMVar_hsa_circ_361031,RMVar_hsa_circ_361921 87750 RMVar_ID_87750 Human_SNP_ID_446948149 m1A Human chr10 + 110881330 110881330 110881330 AAGAATGAAATAAATGGAAATTGGATTTCAGCATCCTCCATTAACGAAGCTAGAATTAATGCCAA AAGAATGAAATAAATGGAAATTGGATTTCAGCGTCCTCCATTAACGAAGCTAGAATTAATGCCAA A G PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:110881181..110883100 26863196 MeRIP-seq:(Medium) rs780026914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28884,Human_RBP_ID_1441438,Human_RBP_ID_1760071,Human_RBP_ID_5925419,Human_RBP_ID_8325741,Human_RBP_ID_27602662 Human_Splice_Rec_1175876,Human_Splice_Rec_1175896,Human_Splice_Rec_1175908,Human_Splice_Rec_1175916,Human_Splice_Rec_1175938,Human_Splice_Rec_1175946 RMVar_hsa_circ_146377,RMVar_hsa_circ_305214,RMVar_hsa_circ_287709,RMVar_hsa_circ_357041,RMVar_hsa_circ_367553,RMVar_hsa_circ_362745,RMVar_hsa_circ_355786,RMVar_hsa_circ_62268,RMVar_hsa_circ_72100,RMVar_hsa_circ_353845,RMVar_hsa_circ_354630,RMVar_hsa_circ_348239,RMVar_hsa_circ_64240,RMVar_hsa_circ_273239,RMVar_hsa_circ_146378,RMVar_hsa_circ_146379,RMVar_hsa_circ_361031,RMVar_hsa_circ_361921 87751 RMVar_ID_87751 Human_SNP_ID_446948217 m1A Human chr10 + 110881516 110881516 110881516 TTGCTGGATAGGCGATCCAGATCTGGGAAAGGAAGGGGACTACCAAAGAAAGGTTGGTATATATC TTGCTGGATAGGCGATCCAGATCTGGGAAAGGGAGGGGACTACCAAAGAAAGGTTGGTATATATC A G PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:110881197..110881579 26863196 MeRIP-seq:(Medium) rs1307252929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_981435,Human_RBP_ID_5925426,Human_RBP_ID_9360785 Human_Splice_Rec_1175877,Human_Splice_Rec_1175897,Human_Splice_Rec_1175909,Human_Splice_Rec_1175917,Human_Splice_Rec_1175939,Human_Splice_Rec_1175947 RMVar_hsa_circ_146377,RMVar_hsa_circ_305214,RMVar_hsa_circ_287709,RMVar_hsa_circ_357041,RMVar_hsa_circ_367553,RMVar_hsa_circ_362745,RMVar_hsa_circ_355786,RMVar_hsa_circ_62268,RMVar_hsa_circ_72100,RMVar_hsa_circ_353845,RMVar_hsa_circ_354630,RMVar_hsa_circ_348239,RMVar_hsa_circ_64240,RMVar_hsa_circ_273239,RMVar_hsa_circ_146378,RMVar_hsa_circ_146379,RMVar_hsa_circ_361031,RMVar_hsa_circ_361921 87752 RMVar_ID_87752 Human_SNP_ID_446951211 m1A Human chr10 + 110894130 110894129 110894131 TGCTGCTGAAAGAATATTTACTCTCTGGAGACATATCTGAAGCTGAACATTGCCTTAAGGAACTG TGCTGCTGAAAGAATATTTACTCTCTGGAGAC__ATCTGAAGCTGAACATTGCCTTAAGGAACTG CAT C PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1433945394 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_369843,Human_RBP_ID_1760083,Human_RBP_ID_5925526,Human_RBP_ID_8325746,Human_RBP_ID_8757671,Human_RBP_ID_11257947,Human_RBP_ID_17769353,Human_RBP_ID_24780778,Human_RBP_ID_27602677 Human_Splice_Rec_1175888,Human_Splice_Rec_1175889,Human_Splice_Rec_1175928,Human_Splice_Rec_1175929,Human_Splice_Rec_1175960,Human_Splice_Rec_1175966,Human_Splice_Rec_1175967,Human_Splice_Rec_1175982,Human_Splice_Rec_1175983 RMVar_hsa_circ_9667,RMVar_hsa_circ_362745,RMVar_hsa_circ_72100,RMVar_hsa_circ_353845,RMVar_hsa_circ_354630,RMVar_hsa_circ_146379,RMVar_hsa_circ_45335,RMVar_hsa_circ_146381,RMVar_hsa_circ_146382 87753 RMVar_ID_87753 Human_SNP_ID_446951212 m1A Human chr10 + 110894130 110894130 110894130 TGCTGCTGAAAGAATATTTACTCTCTGGAGACATATCTGAAGCTGAACATTGCCTTAAGGAACTG TGCTGCTGAAAGAATATTTACTCTCTGGAGACGTATCTGAAGCTGAACATTGCCTTAAGGAACTG A G PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1206764549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_369843,Human_RBP_ID_1760083,Human_RBP_ID_5925526,Human_RBP_ID_8325746,Human_RBP_ID_8757671,Human_RBP_ID_11257947,Human_RBP_ID_17769353,Human_RBP_ID_24780778,Human_RBP_ID_27602677 Human_Splice_Rec_1175888,Human_Splice_Rec_1175889,Human_Splice_Rec_1175928,Human_Splice_Rec_1175929,Human_Splice_Rec_1175960,Human_Splice_Rec_1175966,Human_Splice_Rec_1175967,Human_Splice_Rec_1175982,Human_Splice_Rec_1175983 RMVar_hsa_circ_9667,RMVar_hsa_circ_362745,RMVar_hsa_circ_72100,RMVar_hsa_circ_353845,RMVar_hsa_circ_354630,RMVar_hsa_circ_146379,RMVar_hsa_circ_45335,RMVar_hsa_circ_146381,RMVar_hsa_circ_146382 87754 RMVar_ID_87754 Human_SNP_ID_446957478 m1A Human chr10 - 110919085 110919085 110919085 AGTAAGCCCAAAGAGGTACCGTGGGTGACCACACATCCCATGTTAGACAAGTTAATTCATACTCC AGTAAGCCCAAAGAGGTACCGTGGGTGACCACTCATCCCATGTTAGACAAGTTAATTCATACTCC T A BBIP1 Ensembl:ENSG00000214413 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:110919080..110919286 26863196 MeRIP-seq:(Medium) rs1269227517 Functional Loss SNV dbSNP153 33..33 33 - - - 87755 RMVar_ID_87755 Human_SNP_ID_446957730 m1A Human chr10 - 110919650 110919650 110919650 CTCCGCCTCATCGGCCCCGAGTTACCGTCAGGAGCCCCGACTCCGCCATCCTCCTCGCTCGCCCT CTCCGCCTCATCGGCCCCGAGTTACCGTCAGGGGCCCCGACTCCGCCATCCTCCTCGCTCGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:110919574..110919922;chr10:110919576..110919935;chr10:110919601..110919905 26863196 MeRIP-seq:(Medium) rs912121117 Functional Loss SNV dbSNP153 33..33 33 - - - 87756 RMVar_ID_87756 Human_SNP_ID_446957731 m1A Human chr10 - 110919650 110919650 110919650 CTCCGCCTCATCGGCCCCGAGTTACCGTCAGGAGCCCCGACTCCGCCATCCTCCTCGCTCGCCCT CTCCGCCTCATCGGCCCCGAGTTACCGTCAGGCGCCCCGACTCCGCCATCCTCCTCGCTCGCCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:110919574..110919922;chr10:110919576..110919935;chr10:110919601..110919905 26863196 MeRIP-seq:(Medium) rs912121117 Functional Loss SNV dbSNP153 33..33 33 - - - 87757 RMVar_ID_87757 Human_SNP_ID_446957932 m1A Human chr10 - 110920184 110920184 110920184 AAGGGTTTTTAGGGAGAGGAGAACGGGAGAGCAAGGTGGACTCCAGGGAGGGGGCGAGAAGAGAC AAGGGTTTTTAGGGAGAGGAGAACGGGAGAGCGAGGTGGACTCCAGGGAGGGGGCGAGAAGAGAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:110920134..110920252 32194978 MeRIP-seq:(Medium) rs1253747506 Functional Loss SNV dbSNP153 33..33 33 - - - 87758 RMVar_ID_87758 Human_SNP_ID_447351710 m1A Human chr10 + 112447506 112447506 112447506 GCCTTGCCCGGCTGGACGAGGGTGCTGGGGAGAGCTGGGAGGGTGCGGGCGGTGGAACGCCGCCC GCCTTGCCCGGCTGGACGAGGGTGCTGGGGAGGGCTGGGAGGGTGCGGGCGGTGGAACGCCGCCC A G VTI1A Ensembl:ENSG00000151532 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:112447495..112447639 26863196 MeRIP-seq:(Medium) rs773276803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172353,Human_RBP_ID_19047415 87759 RMVar_ID_87759 Human_SNP_ID_447352262 m1A Human chr10 + 112449768 112449768 112449768 AGAGCGAAACTGTCTCAATAAATAAATAAATTAAAAAAAAACTATGTCTTTCCTTAGCTGTAGTA AGAGCGAAACTGTCTCAATAAATAAATAAATTTAAAAAAAACTATGTCTTTCCTTAGCTGTAGTA A T VTI1A Ensembl:ENSG00000151532 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs41292618 Functional Loss SNV dbSNP153 33..33 33 - - - 87760 RMVar_ID_87760 Human_SNP_ID_447374693 m1A Human chr10 + 112544760 112544760 112544760 ATGCCATCAGTAAGCTGGGACAGATGATTCTGAGAAGAGGGAAGAGCAAGCACAAAGGCTCTGGA ATGCCATCAGTAAGCTGGGACAGATGATTCTGGGAAGAGGGAAGAGCAAGCACAAAGGCTCTGGA A G VTI1A Ensembl:ENSG00000151532 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:112544757..112545019 26863196 MeRIP-seq:(Medium) rs1257372079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11260550 RMVar_hsa_circ_61558,RMVar_hsa_circ_37101,RMVar_hsa_circ_60793,RMVar_hsa_circ_301270,RMVar_hsa_circ_338856,RMVar_hsa_circ_123376,RMVar_hsa_circ_146420 87761 RMVar_ID_87761 Human_SNP_ID_447439683 m1A Human chr10 - 112820874 112820874 112820874 CTTGCTATCCCCTGGTGCTAGAAAAACCCTCCATCCCTCACCTGTCCACCCTCTGCTACCCAACC CTTGCTATCCCCTGGTGCTAGAAAAACCCTCCTTCCCTCACCTGTCCACCCTCTGCTACCCAACC T A AL158212.5 Ensembl:ENSG00000285676 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:112820743..112820878 26863196 MeRIP-seq:(Medium) rs1163489770 Functional Loss SNV dbSNP153 33..33 33 - - - 87762 RMVar_ID_87762 Human_SNP_ID_447471934 m1A Human chr10 - 112950327 112950327 112950327 AGTTGAAGTTAGACTGAGAGCTTTTCAGTTCAAAGGCGGCGCTGATTGACAGATAGAAAAAGGGG AGTTGAAGTTAGACTGAGAGCTTTTCAGTTCAGAGGCGGCGCTGATTGACAGATAGAAAAAGGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:112950276..112950496 26863196 MeRIP-seq:(Medium) rs908350765 Functional Loss SNV dbSNP153 33..33 33 - - - 87763 RMVar_ID_87763 Human_SNP_ID_447471944 m1A Human chr10 - 112950363 112950363 112950363 GATACAGGAGGTGCTCGTGCCGCTCGGATTTGAGTGAGTTGAAGTTAGACTGAGAGCTTTTCAGT GATACAGGAGGTGCTCGTGCCGCTCGGATTTGTGTGAGTTGAAGTTAGACTGAGAGCTTTTCAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:112950313..112950408 26863196 MeRIP-seq:(Medium) rs1282395091 Functional Loss SNV dbSNP153 33..33 33 - - - 87764 RMVar_ID_87764 Human_SNP_ID_447472445 m1A Human chr10 + 112951555 112951555 112951555 GTATCCCGGCTACCCCTTCATCATGATCCCCGACCTGACGAGCCCCTACCTCCCCAACGGATCGC GTATCCCGGCTACCCCTTCATCATGATCCCCGCCCTGACGAGCCCCTACCTCCCCAACGGATCGC A C TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:112951438..112951643 26863196 MeRIP-seq:(Medium) rs993289792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11263704,Human_RBP_ID_24782043 Human_Splice_Rec_1176796,Human_Splice_Rec_1176797,Human_Splice_Rec_1176822,Human_Splice_Rec_1176823,Human_Splice_Rec_1176842,Human_Splice_Rec_1176843,Human_Splice_Rec_1176868,Human_Splice_Rec_1176869,Human_Splice_Rec_1176892,Human_Splice_Rec_1176893,Human_Splice_Rec_1176920,Human_Splice_Rec_1176921,Human_Splice_Rec_1176948,Human_Splice_Rec_1176949,Human_Splice_Rec_1176974,Human_Splice_Rec_1176975,Human_Splice_Rec_1177000,Human_Splice_Rec_1177001,Human_Splice_Rec_1177024,Human_Splice_Rec_1177025,Human_Splice_Rec_1177052,Human_Splice_Rec_1177053,Human_Splice_Rec_1177080,Human_Splice_Rec_1177081,Human_Splice_Rec_1177108,Human_Splice_Rec_1177109,Human_Splice_Rec_1177132,Human_Splice_Rec_1177133 RMVar_hsa_circ_55138,RMVar_hsa_circ_51712 87765 RMVar_ID_87765 Human_SNP_ID_447472450 m1A Human chr10 + 112951570 112951570 112951570 CTTCATCATGATCCCCGACCTGACGAGCCCCTACCTCCCCAACGGATCGCTCTCGCCCACCGCCC CTTCATCATGATCCCCGACCTGACGAGCCCCTGCCTCCCCAACGGATCGCTCTCGCCCACCGCCC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:112951517..113089436;chr10:112951424..112964616 26863196 MeRIP-seq:(Medium) rs1431029741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11263704,Human_RBP_ID_24855392 Human_Splice_Rec_1176796,Human_Splice_Rec_1176797,Human_Splice_Rec_1176822,Human_Splice_Rec_1176823,Human_Splice_Rec_1176842,Human_Splice_Rec_1176843,Human_Splice_Rec_1176868,Human_Splice_Rec_1176869,Human_Splice_Rec_1176892,Human_Splice_Rec_1176893,Human_Splice_Rec_1176920,Human_Splice_Rec_1176921,Human_Splice_Rec_1176948,Human_Splice_Rec_1176949,Human_Splice_Rec_1176974,Human_Splice_Rec_1176975,Human_Splice_Rec_1177000,Human_Splice_Rec_1177001,Human_Splice_Rec_1177024,Human_Splice_Rec_1177025,Human_Splice_Rec_1177052,Human_Splice_Rec_1177053,Human_Splice_Rec_1177080,Human_Splice_Rec_1177081,Human_Splice_Rec_1177108,Human_Splice_Rec_1177109,Human_Splice_Rec_1177132,Human_Splice_Rec_1177133 RMVar_hsa_circ_55138,RMVar_hsa_circ_51712 87766 RMVar_ID_87766 Human_SNP_ID_447493277 m1A Human chr10 - 113032250 113032250 113032250 AGGTTAGTGGTTCTGCAGGGAGGCTATGGTACAGCAGCTCACACACGGACAATCGGTATGGAATT AGGTTAGTGGTTCTGCAGGGAGGCTATGGTACGGCAGCTCACACACGGACAATCGGTATGGAATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:113032247..113032349 26863196 MeRIP-seq:(Medium) rs1392675889 Functional Loss SNV dbSNP153 33..33 33 - - - 87767 RMVar_ID_87767 Human_SNP_ID_447495247 m1A Human chr10 + 113040121 113040121 113040121 TCAAGGATGCCCGGTCCCCATCACCGGCACACATTGTCGTAAGTAACCTCCCAGAGATGATGGCT TCAAGGATGCCCGGTCCCCATCACCGGCACACGTTGTCGTAAGTAACCTCCCAGAGATGATGGCT A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:113040071..113040168 26863196 MeRIP-seq:(Medium) rs143077353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18971307,Human_RBP_ID_19047421 Human_Splice_Rec_1176800,Human_Splice_Rec_1176801,Human_Splice_Rec_1176846,Human_Splice_Rec_1176847,Human_Splice_Rec_1176870,Human_Splice_Rec_1176871,Human_Splice_Rec_1176896,Human_Splice_Rec_1176897,Human_Splice_Rec_1176922,Human_Splice_Rec_1176923,Human_Splice_Rec_1176952,Human_Splice_Rec_1176953,Human_Splice_Rec_1176976,Human_Splice_Rec_1176977,Human_Splice_Rec_1177002,Human_Splice_Rec_1177003,Human_Splice_Rec_1177026,Human_Splice_Rec_1177027,Human_Splice_Rec_1177054,Human_Splice_Rec_1177055,Human_Splice_Rec_1177082,Human_Splice_Rec_1177083,Human_Splice_Rec_1177110,Human_Splice_Rec_1177111,Human_Splice_Rec_1177136,Human_Splice_Rec_1177137 RMVar_hsa_circ_146428,RMVar_hsa_circ_288183,RMVar_hsa_circ_51712,RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_352651,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146430,RMVar_hsa_circ_146431 87768 RMVar_ID_87768 Human_SNP_ID_447496444 m1A Human chr10 + 113045493 113045493 113045493 GTGGTGTGCCAAGAGCAGCTGGGAGCCCTGGGACCCCCAGGGAACCCCAGCCCCACCTGGGCATG GTGGTGTGCCAAGAGCAGCTGGGAGCCCTGGGCCCCCCAGGGAACCCCAGCCCCACCTGGGCATG A C TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:113045443..113045572 26863196 MeRIP-seq:(Medium) rs992648198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5280998,Human_RBP_ID_19471559,Human_RBP_ID_22537113 RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 87769 RMVar_ID_87769 Human_SNP_ID_447521210 m1A Human chr10 + 113141275 113141275 113141275 CACGTACAGCAATGAACACTTCACGCCGGGAAACCCACCTCCACACTTACCAGCCGACGTAGACC CACGTACAGCAATGAACACTTCACGCCGGGAAGCCCACCTCCACACTTACCAGCCGACGTAGACC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr10:113141226..113141325;chr10:113141168..113141382 26863196 MeRIP-seq:(Medium) rs987834408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11266307,Human_RBP_ID_17225517,Human_RBP_ID_17342275,Human_RBP_ID_17769918,Human_RBP_ID_27403967 Human_Splice_Rec_1176802,Human_Splice_Rec_1176803,Human_Splice_Rec_1176824,Human_Splice_Rec_1176825,Human_Splice_Rec_1176848,Human_Splice_Rec_1176849,Human_Splice_Rec_1176872,Human_Splice_Rec_1176873,Human_Splice_Rec_1176898,Human_Splice_Rec_1176899,Human_Splice_Rec_1176926,Human_Splice_Rec_1176927,Human_Splice_Rec_1176954,Human_Splice_Rec_1176955,Human_Splice_Rec_1176978,Human_Splice_Rec_1176979,Human_Splice_Rec_1177006,Human_Splice_Rec_1177007,Human_Splice_Rec_1177028,Human_Splice_Rec_1177029,Human_Splice_Rec_1177056,Human_Splice_Rec_1177057,Human_Splice_Rec_1177084,Human_Splice_Rec_1177085,Human_Splice_Rec_1177112,Human_Splice_Rec_1177113,Human_Splice_Rec_1177140,Human_Splice_Rec_1177142,Human_Splice_Rec_1177143,Human_Splice_Rec_1177148,Human_Splice_Rec_1177149,Human_Splice_Rec_1177156,Human_Splice_Rec_1177157,Human_Splice_Rec_1177166,Human_Splice_Rec_1177167,Human_Splice_Rec_1177176,Human_Splice_Rec_1177177,Human_Splice_Rec_1177184,Human_Splice_Rec_1177185,Human_Splice_Rec_1177190,Human_Splice_Rec_1177191,Human_Splice_Rec_1177198,Human_Splice_Rec_1177199,Human_Splice_Rec_1177210,Human_Splice_Rec_1177211 RMVar_hsa_circ_6201,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_146433,RMVar_hsa_circ_69001,RMVar_hsa_circ_120558,RMVar_hsa_circ_278455,RMVar_hsa_circ_146434 87770 RMVar_ID_87770 Human_SNP_ID_447527698 m1A Human chr10 - 113165642 113165641 113165642 GGAGGGGAGCCTAGCAGGTTCGGGGAGGGGGGAGGCGAATCTAGTAAGCTTCCATCTGAAGAGGG GGAGGGGAGCCTAGCAGGTTCGGGGAGGGGGG_GGCGAATCTAGTAAGCTTCCATCTGAAGAGGG CT C HSALNG0080727 RNACentral:URS0000EB990A lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:113165594..113166003 26863196 MeRIP-seq:(Medium) rs779651618 Functional Loss DEL dbSNP153 33..33 33 - - - 87771 RMVar_ID_87771 Human_SNP_ID_447527796 m1A Human chr10 - 113165755 113165755 113165755 CAGCGAGCAGGAGGGCGGGTGGCGGAGGCATCATGGACAGGTGGGCCAGGGGGTCGGGCTTCAGG CAGCGAGCAGGAGGGCGGGTGGCGGAGGCATCCTGGACAGGTGGGCCAGGGGGTCGGGCTTCAGG T G HSALNG0080727 RNACentral:URS0000EB990A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:113165582..113165882 26863196 MeRIP-seq:(Medium) rs756799314 Functional Loss SNV dbSNP153 33..33 33 - - - 87772 RMVar_ID_87772 Human_SNP_ID_447527819 m1A Human chr10 + 113165788 113165788 113165788 GATGCCTCCGCCACCCGCCCTCCTGCTCGCTGAGGCCACCCACAAGGCCTCCGCCCTCTGTCCCA GATGCCTCCGCCACCCGCCCTCCTGCTCGCTGGGGCCACCCACAAGGCCTCCGCCCTCTGTCCCA A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:113165740..113165855 26863196 MeRIP-seq:(Medium) rs962376634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_370255,Human_RBP_ID_5138402,Human_RBP_ID_18931263 87773 RMVar_ID_87773 Human_SNP_ID_447527838 m1A Human chr10 + 113165821 113165821 113165821 GGCCACCCACAAGGCCTCCGCCCTCTGTCCCAACGGGGCCCTGGACCTGCCCCCAGCCGCTTTGC GGCCACCCACAAGGCCTCCGCCCTCTGTCCCAGCGGGGCCCTGGACCTGCCCCCAGCCGCTTTGC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:113165801..113165825 26863196 MeRIP-seq:(Medium) rs762832310 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18931919 87774 RMVar_ID_87774 Human_SNP_ID_447527880 m1A Human chr10 + 113165873 113165873 113165873 CCAGCCGCTTTGCAGCCTGCCGCCCCCTCCTCATCAATTGCACAGCCGTCGACTTCTTCCTTACA CCAGCCGCTTTGCAGCCTGCCGCCCCCTCCTCGTCAATTGCACAGCCGTCGACTTCTTCCTTACA A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:113165681..113165983 26863196 MeRIP-seq:(Medium) rs1308135107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17225521,Human_RBP_ID_17457791,Human_RBP_ID_18931920,Human_RBP_ID_22420424 Human_Splice_Rec_1177260 87775 RMVar_ID_87775 Human_SNP_ID_447527893 m1A Human chr10 - 113165897 113165897 113165897 GTCCCGGCCAGGGAGCTGTGGGAATGTAAGGAAGAAGTCGACGGCTGTGCAATTGATGAGGAGGG GTCCCGGCCAGGGAGCTGTGGGAATGTAAGGAGGAAGTCGACGGCTGTGCAATTGATGAGGAGGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:113165695..113165950 26863196 MeRIP-seq:(Medium) rs1301880553 Functional Loss SNV dbSNP153 33..33 33 - - - 87776 RMVar_ID_87776 Human_SNP_ID_447661424 m1A Human chr10 - 113697584 113697584 113697584 TAAGCAAACTTACCTGAAGAGGGACGGTACAAACGAGGACCGGTCTGGCTTAGCATCCACTGAAT TAAGCAAACTTACCTGAAGAGGGACGGTACAATCGAGGACCGGTCTGGCTTAGCATCCACTGAAT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:113697534..113709375 32194978 MeRIP-seq:(Medium) rs1170301091 Functional Loss SNV dbSNP153 33..33 33 - - - 87777 RMVar_ID_87777 Human_SNP_ID_447668957 m1A Human chr10 + 113729328 113729328 113729328 TCTTTCCTGTTGAAGGCTATTACTCGTGGAGGAGCCCAGGAAGAGGCTCCTGGTTTGTGCAAGCC TCTTTCCTGTTGAAGGCTATTACTCGTGGAGGCGCCCAGGAAGAGGCTCCTGGTTTGTGCAAGCC A C CASP7 Ensembl:ENSG00000165806 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:113729316..113729466 32194978 MeRIP-seq:(Medium) rs200326742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1177650,Human_Splice_Rec_1177674,Human_Splice_Rec_1177688,Human_Splice_Rec_1177702,Human_Splice_Rec_1177714,Human_Splice_Rec_1177726,Human_Splice_Rec_1177740,Human_Splice_Rec_1177752,Human_Splice_Rec_1177762,Human_Splice_Rec_1177772,Human_Splice_Rec_1177784 RMVar_hsa_circ_146438 87778 RMVar_ID_87778 Human_SNP_ID_447699323 m1A Human chr10 + 113854172 113854172 113854172 TCACCGCCCCCCACCTGCCACTCGGCACCCCAAGGGAGCCGCTCCAGCTGCATCCGCTCCTCCCG TCACCGCCCCCCACCTGCCACTCGGCACCCCACGGGAGCCGCTCCAGCTGCATCCGCTCCTCCCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:113854066..113854273 26863196 MeRIP-seq:(Medium) rs904334556 Functional Loss SNV dbSNP153 33..33 33 - - - 87779 RMVar_ID_87779 Human_SNP_ID_447747626 m1A Human chr10 - 114044802 114044802 114044802 GTAGAAGGAGACTACGGACGAGGCGATGGCGTAGGCCCGGTTGGTGACGAAGTCGCAGCACTTGG GTAGAAGGAGACTACGGACGAGGCGATGGCGTCGGCCCGGTTGGTGACGAAGTCGCAGCACTTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:114044743..114044892 26863196 MeRIP-seq:(Medium) rs1307811699 Functional Loss SNV dbSNP153 33..33 33 - - - 87780 RMVar_ID_87780 Human_SNP_ID_447774022 m1A Human chr10 + 114149770 114149746 114149770 AAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA AAGGAAGGC________________________AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA CAGGAAGGCAGGAAGGAAGGAAGGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:114149760..114149847 26863196 MeRIP-seq:(Medium) rs1564912860 Functional Loss DEL dbSNP153 10..33 33 - - - 87781 RMVar_ID_87781 Human_SNP_ID_447774067 m1A Human chr10 + 114149770 114149770 114149770 AAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA AAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:114149760..114149847 26863196 MeRIP-seq:(Medium) rs536773237 Functional Loss SNV dbSNP153 33..33 33 - - - 87782 RMVar_ID_87782 Human_SNP_ID_447774068 m1A Human chr10 + 114149770 114149770 114149770 AAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA AAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGGAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:114149760..114149847 26863196 MeRIP-seq:(Medium) rs536773237 Functional Loss SNV dbSNP153 33..33 33 - - - 87783 RMVar_ID_87783 Human_SNP_ID_448121838 m1A Human chr10 - 115572372 115572372 115572372 TGACAATATATTTGACCTCAAAAACAAATCCTAAATTTTCCTCTGTCTCTCCACCTCTATTACCA TGACAATATATTTGACCTCAAAAACAAATCCTGAATTTTCCTCTGTCTCTCCACCTCTATTACCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:115572282..115572395 26863196 MeRIP-seq:(Medium) rs1204758151 Functional Loss SNV dbSNP153 33..33 33 - - - 87784 RMVar_ID_87784 Human_SNP_ID_448239234 m1A Human chr10 + 116062711 116062711 116062711 TTTCTGAAGGTGGAATCTCCTCCTCTTTACTTAATGTTGGAGAAAAGTGGCCACCAGTACTCGAT TTTCTGAAGGTGGAATCTCCTCCTCTTTACTTGATGTTGGAGAAAAGTGGCCACCAGTACTCGAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:116062660..116063011 32194978 MeRIP-seq:(Medium) rs1283024118 Functional Loss SNV dbSNP153 33..33 33 - - - 87785 RMVar_ID_87785 Human_SNP_ID_448255264 m1A Human chr10 + 116125298 116125298 116125298 TTGGGCTTCTCCCTCTCTTCATAGGAGCACACAGGCACGATGGTCTGTCGCCTCCGCTCTGTGCA TTGGGCTTCTCCCTCTCTTCATAGGAGCACACGGGCACGATGGTCTGTCGCCTCCGCTCTGTGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:116125250..116269530 32194978 MeRIP-seq:(Medium) rs1304881339 Functional Loss SNV dbSNP153 33..33 33 - - - 87786 RMVar_ID_87786 Human_SNP_ID_448396329 m1A Human chr10 - 116696869 116696869 116696869 TCACAGGCAGCAACTGGAAGGGTGGGTATTTCAAGCTGGTGGAATGGCACAGGCTCAGCTCAGAA TCACAGGCAGCAACTGGAAGGGTGGGTATTTCTAGCTGGTGGAATGGCACAGGCTCAGCTCAGAA T A HSPA12A Ensembl:ENSG00000165868 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:116696756..116697002 26863196 MeRIP-seq:(Medium) rs782363301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172358,Human_RBP_ID_11270894,Human_RBP_ID_18931268 RMVar_hsa_circ_83814,RMVar_hsa_circ_324406,RMVar_hsa_circ_10414,RMVar_hsa_circ_308770,RMVar_hsa_circ_146553,RMVar_hsa_circ_16074,RMVar_hsa_circ_146554 87787 RMVar_ID_87787 Human_SNP_ID_448407798 m1A Human chr10 + 116742504 116742504 116742504 TCGCGCAGCCCCGGACCGCGAGGGGAGCCTCCAGCGCAGCGCCCGTGCCCGTGCGGGTCTCTGTC TCGCGCAGCCCCGGACCGCGAGGGGAGCCTCCCGCGCAGCGCCCGTGCCCGTGCGGGTCTCTGTC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr10:116742449..116742540;chr10:116742454..116742538 26863410,26863196 MeRIP-seq:(Medium) rs1554887355 Functional Loss SNV dbSNP153 33..33 33 - - - 87788 RMVar_ID_87788 Human_SNP_ID_448407801 m1A Human chr10 + 116742509 116742509 116742509 CAGCCCCGGACCGCGAGGGGAGCCTCCAGCGCAGCGCCCGTGCCCGTGCGGGTCTCTGTCCGCGT CAGCCCCGGACCGCGAGGGGAGCCTCCAGCGCGGCGCCCGTGCCCGTGCGGGTCTCTGTCCGCGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:116742309..116742549 26863196 MeRIP-seq:(Medium) rs1554887358 Functional Loss SNV dbSNP153 33..33 33 - - - 87789 RMVar_ID_87789 Human_SNP_ID_448433052 m1A Human chr10 + 116849603 116849603 116849603 AGGAAGAAGGCGGCGGCCGCAGCTGTGGGACCACTAGGGAGCTGCAGAAGCTGAAGCAGCAGGCG AGGAAGAAGGCGGCGGCCGCAGCTGTGGGACCTCTAGGGAGCTGCAGAAGCTGAAGCAGCAGGCG A T ENO4 Ensembl:ENSG00000188316 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:116849581..116849695 26863196 MeRIP-seq:(Medium) rs1460279615 Functional Loss SNV dbSNP153 33..33 33 - - - 87790 RMVar_ID_87790 Human_SNP_ID_448433084 m1A Human chr10 + 116849669 116849669 116849669 TGGAGTACTACCGGGAGAACGACGTTCCGCGCAGGCTGGAAGAGCTGCTCAACTCCACCTTCTAC TGGAGTACTACCGGGAGAACGACGTTCCGCGCCGGCTGGAAGAGCTGCTCAACTCCACCTTCTAC A C ENO4 Ensembl:ENSG00000188316 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:116849533..116849756 26863196 MeRIP-seq:(Medium) rs1471637400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1180099,Human_Splice_Rec_1180125,Human_Splice_Rec_1180137 87791 RMVar_ID_87791 Human_SNP_ID_448560049 m1A Human chr10 - 117374894 117374891 117374894 CCATCCTATTCCTGTTCCGGGAGTTGCGGGACACCGCGCTGACCCGCCGCTGGGTCACCAAGAAG CCATCCTATTCCTGTTCCGGGAGTTGCGGGAC___GCGCTGACCCGCCGCTGGGTCACCAAGAAG CGGT C PDZD8 Ensembl:ENSG00000165650 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:117374843..117374918 26863196 MeRIP-seq:(Medium) rs759069982 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_371345,Human_RBP_ID_862902,Human_RBP_ID_8765470,Human_RBP_ID_9274266,Human_RBP_ID_9320719,Human_RBP_ID_18587693,Human_RBP_ID_22029566,Human_RBP_ID_23206750 87792 RMVar_ID_87792 Human_SNP_ID_448560278 m1A Human chr10 - 117375240 117375240 117375240 CGCTGTGGGCGCGGGAGTAGGGGCCCGGGCGGAGGCGGTGGCGGGATGGGGCTGCTGCTCATGAT CGCTGTGGGCGCGGGAGTAGGGGCCCGGGCGGGGGCGGTGGCGGGATGGGGCTGCTGCTCATGAT T C PDZD8 Ensembl:ENSG00000165650 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:117374981..117375406 26863196 MeRIP-seq:(Medium) rs1169173307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225908,Human_RBP_ID_4136061,Human_RBP_ID_5933274,Human_RBP_ID_8765472,Human_RBP_ID_9274268,Human_RBP_ID_17770764 87793 RMVar_ID_87793 Human_SNP_ID_448601034 m1A Human chr10 - 117542302 117542302 117542302 ACTCCCCCTCAGCCACCGCCTCCTCCTCCACCAGCACCACTCCCTCCGGGGCACCCCGGTCCCTG ACTCCCCCTCAGCCACCGCCTCCTCCTCCACCTGCACCACTCCCTCCGGGGCACCCCGGTCCCTG T A EMX2OS Ensembl:ENSG00000229847 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:117542210..117542329 26863196 MeRIP-seq:(Medium) rs1423503334 Functional Loss SNV dbSNP153 33..33 33 - - - 87794 RMVar_ID_87794 Human_SNP_ID_448722530 m1A Human chr10 - 118046608 118046608 118046608 GGGAGGAGGAGCCGGGCCGAGCCTGCGGACGAACGCCGGGCGGGCGGGAGGCGCGGAGGCAGCGG GGGAGGAGGAGCCGGGCCGAGCCTGCGGACGACCGCCGGGCGGGCGGGAGGCGCGGAGGCAGCGG T G RAB11FIP2 Ensembl:ENSG00000107560 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:118046532..118046648 26863196 MeRIP-seq:(Medium) rs1189372491 Functional Loss SNV dbSNP153 33..33 33 - - - 87795 RMVar_ID_87795 Human_SNP_ID_448888378 m1A Human chr10 - 118754693 118754690 118754693 ACGAGGCGATGATGGACGACCAGAACCACAACAACTGGGAGGCTGCGGTGGACGGCTTCCGGCAG ACGAGGCGATGATGGACGACCAGAACCACAAC___TGGGAGGCTGCGGTGGACGGCTTCCGGCAG AGTT A CACUL1 Ensembl:ENSG00000151893 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:118754676..118754700 26863196 MeRIP-seq:(Medium) rs776958575 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_225865,Human_RBP_ID_862905,Human_RBP_ID_3340603,Human_RBP_ID_4109102,Human_RBP_ID_9320721,Human_RBP_ID_9360833,Human_RBP_ID_17771072 87796 RMVar_ID_87796 Human_SNP_ID_448888403 m1A Human chr10 - 118754745 118754742 118754745 CCGGGGGCCAGCAGGATGGAGGAAAGCATGGAAGAGGAGGAGGGGGGCAGCTACGAGGCGATGAT CCGGGGGCCAGCAGGATGGAGGAAAGCATGGA___GGAGGAGGGGGGCAGCTACGAGGCGATGAT CTCT C CACUL1 Ensembl:ENSG00000151893 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:118754451..118755000 26863196 MeRIP-seq:(Medium) rs1370594886 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4136066,Human_RBP_ID_5935152,Human_RBP_ID_23438008 Human_miRNA_ID_460570,Human_miRNA_ID_631174 87797 RMVar_ID_87797 Human_SNP_ID_448888404 m1A Human chr10 - 118754745 118754745 118754745 CCGGGGGCCAGCAGGATGGAGGAAAGCATGGAAGAGGAGGAGGGGGGCAGCTACGAGGCGATGAT CCGGGGGCCAGCAGGATGGAGGAAAGCATGGAGGAGGAGGAGGGGGGCAGCTACGAGGCGATGAT T C CACUL1 Ensembl:ENSG00000151893 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:118754451..118755000 26863196 MeRIP-seq:(Medium) rs1292718696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136066,Human_RBP_ID_5935152,Human_RBP_ID_23438008 Human_miRNA_ID_460570,Human_miRNA_ID_631174 87798 RMVar_ID_87798 Human_SNP_ID_448888444 m1A Human chr10 - 118754870 118754870 118754870 CCCTGCGCACCGCAGCCCTCTCCGCTGCGCCCATTCCTGCCGCCGGCGATGTAACTCGGGGAGGC CCCTGCGCACCGCAGCCCTCTCCGCTGCGCCCTTTCCTGCCGCCGGCGATGTAACTCGGGGAGGC T A CACUL1 Ensembl:ENSG00000151893 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:118754774..118754957 26863410 MeRIP-seq:(Medium) rs547570266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371666,Human_RBP_ID_4109109,Human_RBP_ID_5434984,Human_RBP_ID_5487601 87799 RMVar_ID_87799 Human_SNP_ID_448954654 m1A Human chr10 + 119029793 119029786 119029793 CGCCGGCGGCGGGGAGGCGGCGCGCGGCCCGCAGCCCGCCCATGGAGGCTTTCCCCTGGGCGCCC CGCCGGCGGCGGGGAGGCGGCGCGCG_______GCCCGCCCATGGAGGCTTTCCCCTGGGCGCCC GGCCCGCA G NANOS1 Ensembl:ENSG00000188613 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119029749..119029842 26863196 MeRIP-seq:(Medium) rs1222425584 Functional Loss DEL dbSNP153 27..33 33 - - - 87800 RMVar_ID_87800 Human_SNP_ID_448954661 m1A Human chr10 + 119029793 119029793 119029793 CGCCGGCGGCGGGGAGGCGGCGCGCGGCCCGCAGCCCGCCCATGGAGGCTTTCCCCTGGGCGCCC CGCCGGCGGCGGGGAGGCGGCGCGCGGCCCGCGGCCCGCCCATGGAGGCTTTCCCCTGGGCGCCC A G NANOS1 Ensembl:ENSG00000188613 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119029749..119029842 26863196 MeRIP-seq:(Medium) rs1414969688 Functional Loss SNV dbSNP153 33..33 33 - - - 87801 RMVar_ID_87801 Human_SNP_ID_448954674 m1A Human chr10 - 119029817 119029817 119029817 GGCGCGGCCGCGGCGGGGCGAGCGGGGCGCCCAGGGGAAAGCCTCCATGGGCGGGCTGCGGGCCG GGCGCGGCCGCGGCGGGGCGAGCGGGGCGCCCTGGGGAAAGCCTCCATGGGCGGGCTGCGGGCCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119029777..119029909 26863196 MeRIP-seq:(Medium) rs1446848471 Functional Loss SNV dbSNP153 33..33 33 - - - 87802 RMVar_ID_87802 Human_SNP_ID_448956610 m1A Human chr10 + 119036264 119036264 119036264 TCATCTTTCCTGTCATCAGCACGTCTCCAAGAACTTACTAAAAAGTTTAATTAAAAAAAAAAAAT TCATCTTTCCTGTCATCAGCACGTCTCCAAGATCTTACTAAAAAGTTTAATTAAAAAAAAAAAAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119036091..119036301 26863196 MeRIP-seq:(Medium) rs1389706388 Functional Loss SNV dbSNP153 33..33 33 - - - 87803 RMVar_ID_87803 Human_SNP_ID_448957335 m1A Human chr10 - 119038381 119038381 119038381 AGAGAGGAGAGCTGGGGTCCACCTCGAGAATCAAGGCCATCAGAAGAACGTGAATGGGACAGAGA AGAGAGGAGAGCTGGGGTCCACCTCGAGAATCCAGGCCATCAGAAGAACGTGAATGGGACAGAGA T G EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:119036226..119042050 26863196 MeRIP-seq:(Medium) rs1220353948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26563,Human_RBP_ID_225076,Human_RBP_ID_981799,Human_RBP_ID_1442306,Human_RBP_ID_1761306,Human_RBP_ID_2193861,Human_RBP_ID_4109238,Human_RBP_ID_5935353,Human_RBP_ID_8758539,Human_RBP_ID_11278252,Human_RBP_ID_18431327,Human_RBP_ID_22150763,Human_RBP_ID_23438123,Human_RBP_ID_24542137,Human_RBP_ID_26316746 Human_Splice_Rec_1180966,Human_Splice_Rec_1181008 RMVar_hsa_circ_78605,RMVar_hsa_circ_61099,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_293765,RMVar_hsa_circ_313961,RMVar_hsa_circ_110011,RMVar_hsa_circ_146616,RMVar_hsa_circ_146617 87804 RMVar_ID_87804 Human_SNP_ID_448958276 m1A Human chr10 - 119042097 119042097 119042097 CGTGGTGCAGAGGATGACAGGGGCCCTTGGAGAAACATGGATGATGATCGCCTTTCAAGACGTGC CGTGGTGCAGAGGATGACAGGGGCCCTTGGAGTAACATGGATGATGATCGCCTTTCAAGACGTGC T A EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:119042076..119042100 26863196 MeRIP-seq:(Medium) rs770203283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371746,Human_RBP_ID_747168,Human_RBP_ID_981801,Human_RBP_ID_1761309,Human_RBP_ID_4109251,Human_RBP_ID_5643398,Human_RBP_ID_5935367,Human_RBP_ID_8327249,Human_RBP_ID_8758541,Human_RBP_ID_9254170,Human_RBP_ID_9274007,Human_RBP_ID_9352573,Human_RBP_ID_9360843,Human_RBP_ID_11278319,Human_RBP_ID_17786900,Human_RBP_ID_18238621,Human_RBP_ID_22029571,Human_RBP_ID_22878107,Human_RBP_ID_23438130,Human_RBP_ID_24542273,Human_RBP_ID_26315990,Human_RBP_ID_27190514,Human_RBP_ID_27603847,Human_RBP_ID_27802394 Human_miRNA_ID_1405206,Human_miRNA_ID_1538769,Human_miRNA_ID_1593000,Human_miRNA_ID_2789330,Human_miRNA_ID_2818944 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_61099,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_313961,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_49267,RMVar_hsa_circ_328467 87805 RMVar_ID_87805 Human_SNP_ID_448958376 m1A Human chr10 + 119042295 119042295 119042295 TCATCATCCATGCCTCGCCTGGGACCCCGATCATCATCCAACCCTCGCCTGGGACCCCGGTCATC TCATCATCCATGCCTCGCCTGGGACCCCGATCGTCATCCAACCCTCGCCTGGGACCCCGGTCATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119041959..119044195 26863196 MeRIP-seq:(Medium) rs754180203 Functional Loss SNV dbSNP153 33..33 33 - - - 87806 RMVar_ID_87806 Human_SNP_ID_448958377 m1A Human chr10 + 119042295 119042295 119042295 TCATCATCCATGCCTCGCCTGGGACCCCGATCATCATCCAACCCTCGCCTGGGACCCCGGTCATC TCATCATCCATGCCTCGCCTGGGACCCCGATCTTCATCCAACCCTCGCCTGGGACCCCGGTCATC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119041959..119044195 26863196 MeRIP-seq:(Medium) rs754180203 Functional Loss SNV dbSNP153 33..33 33 - - - 87807 RMVar_ID_87807 Human_SNP_ID_448958534 m1A Human chr10 + 119042675 119042675 119042675 CCGGGGAACCCGATCATCGTCTGGTCTAAGAGAGGGCTCTCTATCTTCATCATCCCCCAGACGCC CCGGGGAACCCGATCATCGTCTGGTCTAAGAGTGGGCTCTCTATCTTCATCATCCCCCAGACGCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:119042625..119044106 32194978 MeRIP-seq:(Medium) rs777796020 Functional Loss SNV dbSNP153 33..33 33 - - - 87808 RMVar_ID_87808 Human_SNP_ID_448958563 m1A Human chr10 - 119042740 119042740 119042740 GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGACAGGTCTCATAGAAGAGATGAAGAGCGGCCCC GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGTCAGGTCTCATAGAAGAGATGAAGAGCGGCCCC T A EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:119042640..119042756 26863196 MeRIP-seq:(Medium) rs369943865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225081,Human_RBP_ID_747172,Human_RBP_ID_805724,Human_RBP_ID_864046,Human_RBP_ID_4139356,Human_RBP_ID_5935383,Human_RBP_ID_8758564,Human_RBP_ID_9360850,Human_RBP_ID_11278338,Human_RBP_ID_18410350,Human_RBP_ID_22029576,Human_RBP_ID_22886834,Human_RBP_ID_23481380,Human_RBP_ID_24542041,Human_RBP_ID_26315993,Human_RBP_ID_27802398 Human_Splice_Rec_1180964,Human_Splice_Rec_1181006 Human_miRNA_ID_3079722 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_61099,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_313961,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_49267,RMVar_hsa_circ_328467 87809 RMVar_ID_87809 Human_SNP_ID_448958564 m1A Human chr10 - 119042740 119042740 119042740 GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGACAGGTCTCATAGAAGAGATGAAGAGCGGCCCC GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGGCAGGTCTCATAGAAGAGATGAAGAGCGGCCCC T C EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:119042640..119042756 26863196 MeRIP-seq:(Medium) rs369943865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225081,Human_RBP_ID_747172,Human_RBP_ID_805724,Human_RBP_ID_864046,Human_RBP_ID_4139356,Human_RBP_ID_5935383,Human_RBP_ID_8758564,Human_RBP_ID_9360850,Human_RBP_ID_11278338,Human_RBP_ID_18410350,Human_RBP_ID_22029576,Human_RBP_ID_22886834,Human_RBP_ID_23481380,Human_RBP_ID_24542041,Human_RBP_ID_26315993,Human_RBP_ID_27802398 Human_Splice_Rec_1180964,Human_Splice_Rec_1181006 Human_miRNA_ID_3079722 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_61099,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_313961,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_49267,RMVar_hsa_circ_328467 87810 RMVar_ID_87810 Human_SNP_ID_448958900 m1A Human chr10 + 119044007 119044007 119044007 AAAATGAACCAAATTTTAAAACCACTGATAAGATATTAACAGGAACTGGAGCGGCATTATTTTCC AAAATGAACCAAATTTTAAAACCACTGATAAGGTATTAACAGGAACTGGAGCGGCATTATTTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119044004..119044185 26863196 MeRIP-seq:(Medium) rs1368801470 Functional Loss SNV dbSNP153 33..33 33 - - - 87811 RMVar_ID_87811 Human_SNP_ID_448960836 m1A Human chr10 - 119051175 119051175 119051175 GTTTATGAGGTGAGCTTGCTGATTTTTGGGAAATGTTTATTCATGAGCTTTCTAGTATTGGCCTA GTTTATGAGGTGAGCTTGCTGATTTTTGGGAATTGTTTATTCATGAGCTTTCTAGTATTGGCCTA T A EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119051173..119051258 26863196 MeRIP-seq:(Medium) rs201530350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26575,Human_RBP_ID_5339737,Human_RBP_ID_11278618,Human_RBP_ID_19045901,Human_RBP_ID_24456324 RMVar_hsa_circ_78605,RMVar_hsa_circ_11358,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_73458,RMVar_hsa_circ_357663,RMVar_hsa_circ_77172,RMVar_hsa_circ_62931,RMVar_hsa_circ_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_146620 87812 RMVar_ID_87812 Human_SNP_ID_448960837 m1A Human chr10 - 119051175 119051175 119051175 GTTTATGAGGTGAGCTTGCTGATTTTTGGGAAATGTTTATTCATGAGCTTTCTAGTATTGGCCTA GTTTATGAGGTGAGCTTGCTGATTTTTGGGAAGTGTTTATTCATGAGCTTTCTAGTATTGGCCTA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119051173..119051258 26863196 MeRIP-seq:(Medium) rs201530350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26575,Human_RBP_ID_5339737,Human_RBP_ID_11278618,Human_RBP_ID_19045901,Human_RBP_ID_24456324 RMVar_hsa_circ_78605,RMVar_hsa_circ_11358,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_73458,RMVar_hsa_circ_357663,RMVar_hsa_circ_77172,RMVar_hsa_circ_62931,RMVar_hsa_circ_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_146620 87813 RMVar_ID_87813 Human_SNP_ID_448962432 m1A Human chr10 - 119057039 119057039 119057039 TTAACAATTGTGCATTTGTATTACCTTTCAGGACCTTGAGGAATTGGATCCAGATTTTATCATGG TTAACAATTGTGCATTTGTATTACCTTTCAGGGCCTTGAGGAATTGGATCCAGATTTTATCATGG T C EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119057001..119057050 26863196 MeRIP-seq:(Medium) rs765966923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26578,Human_RBP_ID_2193940,Human_RBP_ID_4109346,Human_RBP_ID_5163249 Human_Splice_Rec_1180952,Human_Splice_Rec_1180994,Human_Splice_Rec_1181016 RMVar_hsa_circ_148,RMVar_hsa_circ_78605,RMVar_hsa_circ_11358,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_73458,RMVar_hsa_circ_77172,RMVar_hsa_circ_62931,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_146619,RMVar_hsa_circ_371542,RMVar_hsa_circ_365659,RMVar_hsa_circ_308973,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_146622,RMVar_hsa_circ_302616,RMVar_hsa_circ_361372,RMVar_hsa_circ_334293,RMVar_hsa_circ_57897,RMVar_hsa_circ_71060,RMVar_hsa_circ_146626,RMVar_hsa_circ_34491 87814 RMVar_ID_87814 Human_SNP_ID_448969685 m1A Human chr10 - 119080721 119080721 119080721 GTTCCCCTTCGTCTCCTCTCCCGGCCCGGGCCACTAGAGAGTTCGCTGACGCCGGGTGAGCTGAG GTTCCCCTTCGTCTCCTCTCCCGGCCCGGGCCTCTAGAGAGTTCGCTGACGCCGGGTGAGCTGAG T A EIF3A Ensembl:ENSG00000107581 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:119080679..119080753;chr10:119080672..119080766 26863196 MeRIP-seq:(Medium) rs776786266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371777,Human_RBP_ID_4109439,Human_RBP_ID_5414873,Human_RBP_ID_5435116,Human_RBP_ID_5458996,Human_RBP_ID_8327323,Human_RBP_ID_8758640,Human_RBP_ID_9254190,Human_RBP_ID_9274025,Human_RBP_ID_9320722,Human_RBP_ID_17771171,Human_RBP_ID_18588035,Human_RBP_ID_22150827,Human_RBP_ID_26875497,Human_RBP_ID_27190546 Human_Splice_Rec_1180929,Human_Splice_Rec_1180971 RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 87815 RMVar_ID_87815 Human_SNP_ID_448976108 m1A Human chr10 - 119104174 119104174 119104174 CGTCCTCACCGATCAGCCCGACTCCAAGCATCAGCTGAGTGTCCGCCACCTCGGCCGCAGCCATC CGTCCTCACCGATCAGCCCGACTCCAAGCATCCGCTGAGTGTCCGCCACCTCGGCCGCAGCCATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119104124..119104272 26863196 MeRIP-seq:(Medium) rs1350925941 Functional Loss SNV dbSNP153 33..33 33 - - - 87816 RMVar_ID_87816 Human_SNP_ID_448976111 m1A Human chr10 - 119104186 119104186 119104186 GCAGGGCGCCTACGTCCTCACCGATCAGCCCGACTCCAAGCATCAGCTGAGTGTCCGCCACCTCG GCAGGGCGCCTACGTCCTCACCGATCAGCCCGGCTCCAAGCATCAGCTGAGTGTCCGCCACCTCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119104144..119104235 26863196 MeRIP-seq:(Medium) rs1286375232 Functional Loss SNV dbSNP153 33..33 33 - - - 87817 RMVar_ID_87817 Human_SNP_ID_448976262 m1A Human chr10 + 119104714 119104714 119104714 GGGCGGCCCCCATCGTGGGACCGGGCAGCTGGAGACTGCTGGGCCGGGTGCTGCGCGTTGTACAC GGGCGGCCCCCATCGTGGGACCGGGCAGCTGGTGACTGCTGGGCCGGGTGCTGCGCGTTGTACAC A T DENND10 Ensembl:ENSG00000119979 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119104711..119104848 26863196 MeRIP-seq:(Medium) rs1312355679 Functional Loss SNV dbSNP153 33..33 33 - - - 87818 RMVar_ID_87818 Human_SNP_ID_448986083 m1A Human chr10 - 119143152 119143152 119143152 GCCAGGCCAAGGAGCAGGGCAGCAGGTAAGTCATGCAAGGTTGGAAGGGGCAGAACTCCCAGAGG GCCAGGCCAAGGAGCAGGGCAGCAGGTAAGTCCTGCAAGGTTGGAAGGGGCAGAACTCCCAGAGG T G SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119143148..119143301 26863196 MeRIP-seq:(Medium) rs1289380923 Functional Loss SNV dbSNP153 33..33 33 - - - 87819 RMVar_ID_87819 Human_SNP_ID_448992177 m1A Human chr10 - 119165636 119165636 119165636 GGCCACTCTAACCAGCGCAAAATGTCCCTGGAACAGGAGGAGGAAACGCAACCTGGGCGGCTCCT GGCCACTCTAACCAGCGCAAAATGTCCCTGGAGCAGGAGGAGGAAACGCAACCTGGGCGGCTCCT T C SFXN4 Ensembl:ENSG00000183605 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119165585..119165652 26863196 MeRIP-seq:(Medium) rs1004556600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371823,Human_RBP_ID_4136533 Human_Splice_Rec_1181125,Human_Splice_Rec_1181155,Human_Splice_Rec_1181207 Human_miRNA_ID_1979039 RMVar_hsa_circ_83195,RMVar_hsa_circ_146661 87820 RMVar_ID_87820 Human_SNP_ID_448993206 m1A Human chr10 - 119169220 119169220 119169220 CTTGGTGAAGGCGTTCCAGTATGTAGAAACACATGGAGAAGTCTGCCCAGCGAACTGGACACCGG CTTGGTGAAGGCGTTCCAGTATGTAGAAACACGTGGAGAAGTCTGCCCAGCGAACTGGACACCGG T C PRDX3 Ensembl:ENSG00000165672 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:119168494..119169386 32194978 MeRIP-seq:(Medium) rs1254601675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371853,Human_RBP_ID_981830,Human_RBP_ID_1442402,Human_RBP_ID_1761439,Human_RBP_ID_3340764,Human_RBP_ID_4109553,Human_RBP_ID_5935789,Human_RBP_ID_8244526,Human_RBP_ID_8327357,Human_RBP_ID_8758653,Human_RBP_ID_8984019,Human_RBP_ID_11280010,Human_RBP_ID_21882475,Human_RBP_ID_22431605,Human_RBP_ID_23438348,Human_RBP_ID_26875536 Human_Splice_Rec_1181259,Human_Splice_Rec_1181261 Human_miRNA_ID_2745310 RMVar_hsa_circ_77866,RMVar_hsa_circ_119970,RMVar_hsa_circ_104059,RMVar_hsa_circ_146664,RMVar_hsa_circ_146665,RMVar_hsa_circ_146666,RMVar_hsa_circ_341785,RMVar_hsa_circ_146663,RMVar_hsa_circ_297891 87821 RMVar_ID_87821 Human_SNP_ID_448995395 m1A Human chr10 - 119177099 119177099 119177099 TTCCTTGGGGCATTTCTGCCACTGCAGCCCTCAGGCCTGCTGCATGTGGAAGAACGAGCTTGACA TTCCTTGGGGCATTTCTGCCACTGCAGCCCTCTGGCCTGCTGCATGTGGAAGAACGAGCTTGACA T A PRDX3 Ensembl:ENSG00000165672 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119177051..119177175 26863196 MeRIP-seq:(Medium) rs17850322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225385,Human_RBP_ID_371881,Human_RBP_ID_1442420,Human_RBP_ID_1761451,Human_RBP_ID_4136534,Human_RBP_ID_5313350,Human_RBP_ID_9320725,Human_RBP_ID_18455957,Human_RBP_ID_18588071,Human_RBP_ID_22431607,Human_RBP_ID_23438369 Human_Splice_Rec_1181250,Human_Splice_Rec_1181251 Human_miRNA_ID_2221759,Human_miRNA_ID_2484815,Human_miRNA_ID_3073192 RMVar_hsa_circ_77866,RMVar_hsa_circ_104059,RMVar_hsa_circ_146664,RMVar_hsa_circ_146665,RMVar_hsa_circ_322146,RMVar_hsa_circ_326749,RMVar_hsa_circ_146671 87822 RMVar_ID_87822 Human_SNP_ID_448995396 m1A Human chr10 - 119177099 119177099 119177099 TTCCTTGGGGCATTTCTGCCACTGCAGCCCTCAGGCCTGCTGCATGTGGAAGAACGAGCTTGACA TTCCTTGGGGCATTTCTGCCACTGCAGCCCTCGGGCCTGCTGCATGTGGAAGAACGAGCTTGACA T C PRDX3 Ensembl:ENSG00000165672 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119177051..119177175 26863196 MeRIP-seq:(Medium) rs17850322 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_225385,Human_RBP_ID_371881,Human_RBP_ID_1442420,Human_RBP_ID_1761451,Human_RBP_ID_4136534,Human_RBP_ID_5313350,Human_RBP_ID_9320725,Human_RBP_ID_18455957,Human_RBP_ID_18588071,Human_RBP_ID_22431607,Human_RBP_ID_23438369 Human_Splice_Rec_1181250,Human_Splice_Rec_1181251 Human_miRNA_ID_2221759,Human_miRNA_ID_2484815,Human_miRNA_ID_3073192 RMVar_hsa_circ_77866,RMVar_hsa_circ_104059,RMVar_hsa_circ_146664,RMVar_hsa_circ_146665,RMVar_hsa_circ_322146,RMVar_hsa_circ_326749,RMVar_hsa_circ_146671 87823 RMVar_ID_87823 Human_SNP_ID_449003401 m1A Human chr10 + 119206994 119206994 119206994 AGGAAACAAAGTGCATCTTTGTCCGCGGCCCGAGGCGCCGCGTGGGAGACGCTGGGCAGGGGCCA AGGAAACAAAGTGCATCTTTGTCCGCGGCCCGTGGCGCCGCGTGGGAGACGCTGGGCAGGGGCCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119206952..119207156 26863196 MeRIP-seq:(Medium) rs985215321 Functional Loss SNV dbSNP153 33..33 33 - - - 87824 RMVar_ID_87824 Human_SNP_ID_449003720 m1A Human chr10 - 119207740 119207739 119207741 TGCTCTCAGCCCAAGAGTTTCCCCCTCTGCAAAGAGGAGCCGCCGCCGCCGCCGCCGCCGCCGCC TGCTCTCAGCCCAAGAGTTTCCCCCTCTGCA__GAGGAGCCGCCGCCGCCGCCGCCGCCGCCGCC CTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119207691..119207845 26863196 MeRIP-seq:(Medium) rs1564847880 Functional Loss DEL dbSNP153 32..33 33 - - - 87825 RMVar_ID_87825 Human_SNP_ID_449003721 m1A Human chr10 - 119207742 119207742 119207742 CCTGCTCTCAGCCCAAGAGTTTCCCCCTCTGCAAAGAGGAGCCGCCGCCGCCGCCGCCGCCGCCG CCTGCTCTCAGCCCAAGAGTTTCCCCCTCTGCGAAGAGGAGCCGCCGCCGCCGCCGCCGCCGCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119207697..119207934 26863196 MeRIP-seq:(Medium) rs1450977336 Functional Loss SNV dbSNP153 33..33 33 - - - 87826 RMVar_ID_87826 Human_SNP_ID_449003728 m1A Human chr10 - 119207760 119207758 119207760 CTTGCCTACCGCATTATTCCTGCTCTCAGCCCAAGAGTTTCCCCCTCTGCAAAGAGGAGCCGCCG CTTGCCTACCGCATTATTCCTGCTCTCAGCCC__GAGTTTCCCCCTCTGCAAAGAGGAGCCGCCG CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119207682..119207925 26863196 MeRIP-seq:(Medium) rs1470197959 Functional Loss DEL dbSNP153 33..34 33 - - - 87827 RMVar_ID_87827 Human_SNP_ID_449023015 m1A Human chr10 + 119287405 119287405 119287405 GAGGGAGGAAGGAAGGGAAGAAGGAAGGGAGGAAAGAAGGGAGAAGGTAAGGAGGGAGGGAAGGA GAGGGAGGAAGGAAGGGAAGAAGGAAGGGAGGGAAGAAGGGAGAAGGTAAGGAGGGAGGGAAGGA A G GRK5 Ensembl:ENSG00000198873 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119287399..119287506 26863196 MeRIP-seq:(Medium) rs1229392253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172369 87828 RMVar_ID_87828 Human_SNP_ID_449029934 m1A Human chr10 - 119313389 119313389 119313389 ATACCTAGCACCTCATAGGTGCCACTAAATGTAGCCATTGCCACCACCACTCATTACCACCATCA ATACCTAGCACCTCATAGGTGCCACTAAATGTTGCCATTGCCACCACCACTCATTACCACCATCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119313385..119313571 26863196 MeRIP-seq:(Medium) rs555237662 Functional Loss SNV dbSNP153 33..33 33 - - - 87829 RMVar_ID_87829 Human_SNP_ID_449041125 m1A Human chr10 - 119360553 119360553 119360553 ACAGACTTTTCCCACTCACACAGGCTCCTTCCACTCACACAGGCTCTTCCCACTCACACAGGCTC ACAGACTTTTCCCACTCACACAGGCTCCTTCCTCTCACACAGGCTCTTCCCACTCACACAGGCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119360361..119360682 26863196 MeRIP-seq:(Medium) rs1251681206 Functional Loss SNV dbSNP153 33..33 33 - - - 87830 RMVar_ID_87830 Human_SNP_ID_449048835 m1A Human chr10 - 119393998 119393995 119393999 ACACAAACACACCCGCACCCCCCCAGACCCAGACACACACACACATACCCACACACACCTACACA ACACAAACACACCCGCACCCCCCCAGACCCA____CACACACACATACCCACACACACCTACACA GTGTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119393995..119394479 26863196 MeRIP-seq:(Medium) rs999318098 Functional Loss DEL dbSNP153 32..35 33 - - - 87831 RMVar_ID_87831 Human_SNP_ID_449048979 m1A Human chr10 + 119394169 119394154 119394169 TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGAGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT TCTGTGGGTATGTGTGTC_______________GTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT CTGTGTGTGGGTTTGA C GRK5 Ensembl:ENSG00000198873 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119394058..119394232 26863196 MeRIP-seq:(Medium) rs1564916679 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_5281168 RMVar_hsa_circ_354825,RMVar_hsa_circ_68284 87832 RMVar_ID_87832 Human_SNP_ID_449048993 m1A Human chr10 + 119394169 119394165 119394169 TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGAGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT TCTGTGGGTATGTGTGTCTGTGTGTGGGT____GTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT TTTGA T GRK5 Ensembl:ENSG00000198873 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119394058..119394232 26863196 MeRIP-seq:(Medium) rs1181666771 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5281168 RMVar_hsa_circ_354825,RMVar_hsa_circ_68284 87833 RMVar_ID_87833 Human_SNP_ID_449048996 m1A Human chr10 + 119394169 119394169 119394169 TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGAGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGGGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT A G GRK5 Ensembl:ENSG00000198873 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119394058..119394232 26863196 MeRIP-seq:(Medium) rs1477292426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5281168 RMVar_hsa_circ_354825,RMVar_hsa_circ_68284 87834 RMVar_ID_87834 Human_SNP_ID_449048997 m1A Human chr10 + 119394169 119394169 119394169 TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGAGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT TCTGTGGGTATGTGTGTCTGTGTGTGGGTTTGTGTGTGTGTGTGGGTGTCTGTGTATGGGGGTGT A T GRK5 Ensembl:ENSG00000198873 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119394058..119394232 26863196 MeRIP-seq:(Medium) rs1477292426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5281168 RMVar_hsa_circ_354825,RMVar_hsa_circ_68284 87835 RMVar_ID_87835 Human_SNP_ID_449087403 m1A Human chr10 + 119542613 119542613 119542613 GCCGCTTACCTGACGGCGGCCGCTTCCTGCTCAGCCGGCTCACGGCGCGGTTGAACATCGCCGCG GCCGCTTACCTGACGGCGGCCGCTTCCTGCTCTGCCGGCTCACGGCGCGGTTGAACATCGCCGCG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:119542576..119542725 26863410 MeRIP-seq:(Medium) rs1191184267 Functional Loss SNV dbSNP153 33..33 33 - - - 87836 RMVar_ID_87836 Human_SNP_ID_449098541 m1A Human chr10 - 119586059 119586059 119586059 AAGCTTGCAGTGGTATTTGAATCCATGAAGCCATGGGACTAGATGAGTTCACAGAGAGAGAATGA AAGCTTGCAGTGGTATTTGAATCCATGAAGCCGTGGGACTAGATGAGTTCACAGAGAGAGAATGA T C TIAL1 Ensembl:ENSG00000151923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119586058..119586207 26863196 MeRIP-seq:(Medium) rs934307454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1157454,Human_RBP_ID_11280908 RMVar_hsa_circ_21522,RMVar_hsa_circ_107151,RMVar_hsa_circ_146677,RMVar_hsa_circ_315402,RMVar_hsa_circ_103966,RMVar_hsa_circ_339523,RMVar_hsa_circ_36528,RMVar_hsa_circ_146685,RMVar_hsa_circ_146686,RMVar_hsa_circ_276890,RMVar_hsa_circ_290713,RMVar_hsa_circ_146687,RMVar_hsa_circ_56726,RMVar_hsa_circ_358140,RMVar_hsa_circ_358350 87837 RMVar_ID_87837 Human_SNP_ID_449098993 m1A Human chr10 + 119588203 119588203 119588203 CTTTTACAGGGTCCAATCTGACTGAACAACTGAAGTATAAGGACTTCTGTCACATCTCTGGAAAG CTTTTACAGGGTCCAATCTGACTGAACAACTGCAGTATAAGGACTTCTGTCACATCTCTGGAAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:119588151..119588250 32194978 MeRIP-seq:(Medium) rs1438914034 Functional Loss SNV dbSNP153 33..33 33 - - - 87838 RMVar_ID_87838 Human_SNP_ID_449101195 m1A Human chr10 + 119596492 119596492 119596492 CATCATGGTGGGTGCGACGGAGCGATCCCGGGACAAGGGGGAGGGCAGGGTTGGGGAGGGGAGGG CATCATGGTGGGTGCGACGGAGCGATCCCGGGTCAAGGGGGAGGGCAGGGTTGGGGAGGGGAGGG A T lnc-BAG3-4 RNACentral:URS0000D5879F lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:119596426..119596550 32194978 MeRIP-seq:(Medium) rs1377407090 Functional Loss SNV dbSNP153 33..33 33 - - - 87839 RMVar_ID_87839 Human_SNP_ID_449101226 m1A Human chr10 + 119596532 119596532 119596532 GAGGGCAGGGTTGGGGAGGGGAGGGGGTGGGGAGGAAGGGGAGGGGGGCTCTGGGCACCGGCTGG GAGGGCAGGGTTGGGGAGGGGAGGGGGTGGGGGGGAAGGGGAGGGGGGCTCTGGGCACCGGCTGG A G lnc-BAG3-4 RNACentral:URS0000D5879F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119596481..119596669 26863196 MeRIP-seq:(Medium) rs1487431262 Functional Loss SNV dbSNP153 33..33 33 - - - 87840 RMVar_ID_87840 Human_SNP_ID_449115263 m1A Human chr10 + 119651668 119651662 119651668 GCCCCGCACCCGCGCCCCAGCGGGCAGACCCCAACCCAGCATGAGCGCCGCCACCCACTCGCCCA GCCCCGCACCCGCGCCCCAGCGGGCAG______ACCCAGCATGAGCGCCGCCACCCACTCGCCCA GACCCCA G BAG3 Ensembl:ENSG00000151929 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119651425..119651726 26863196 MeRIP-seq:(Medium) rs982182318 Functional Loss DEL dbSNP153 28..33 33 - - - 87841 RMVar_ID_87841 Human_SNP_ID_449115268 m1A Human chr10 + 119651669 119651669 119651669 CCCCGCACCCGCGCCCCAGCGGGCAGACCCCAACCCAGCATGAGCGCCGCCACCCACTCGCCCAT CCCCGCACCCGCGCCCCAGCGGGCAGACCCCAGCCCAGCATGAGCGCCGCCACCCACTCGCCCAT A G BAG3 Ensembl:ENSG00000151929 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:119651519..119651819 32194978 MeRIP-seq:(Medium) rs1161318073 Functional Loss SNV dbSNP153 33..33 33 - - - 87842 RMVar_ID_87842 Human_SNP_ID_449121053 m1A Human chr10 - 119672360 119672360 119672360 GTTCTGCTCGTGTATCACCGGAATGGAGATGTACCCCCGCGGGAGCTGGTGACTGCCCAGGCTGC GTTCTGCTCGTGTATCACCGGAATGGAGATGTGCCCCCGCGGGAGCTGGTGACTGCCCAGGCTGC T C lnc-TIAL1-1,lnc-TIAL1-1:2,lnc-TIAL1-1:3,lnc-TIAL1-1:4 RNACentral:URS0000D5A908,RNACentral:URS00008C3BF0,RNACentral:URS0000D5973A,RNACentral:URS00009B8A32 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119672310..119672591 26863196 MeRIP-seq:(Medium) rs755456690 Functional Loss SNV dbSNP153 33..33 33 - - - 87843 RMVar_ID_87843 Human_SNP_ID_449122572 m1A Human chr10 - 119676721 119676721 119676721 GTGCTGGGGGCTGCCCTCTCTTCTGTAGCCACACTCTTGGGGGAAGAGGGGACAGCAGAAGGGCC GTGCTGGGGGCTGCCCTCTCTTCTGTAGCCACCCTCTTGGGGGAAGAGGGGACAGCAGAAGGGCC T G lnc-TIAL1-1,lnc-TIAL1-1:2,lnc-TIAL1-1:3,lnc-TIAL1-1:4 RNACentral:URS0000D5A908,RNACentral:URS00008C3BF0,RNACentral:URS0000D5973A,RNACentral:URS00009B8A32 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:119676670..119676920 32194978 MeRIP-seq:(Medium) rs777587890 Functional Loss SNV dbSNP153 33..33 33 - - - 87844 RMVar_ID_87844 Human_SNP_ID_449122710 m1A Human chr10 - 119677050 119677050 119677050 GTTCATAGACCTGGACTTGACCTGGGACATCAATGGCTTTCTGTTCAAGTTTTTCCAAGATGGTC GTTCATAGACCTGGACTTGACCTGGGACATCAGTGGCTTTCTGTTCAAGTTTTTCCAAGATGGTC T C lnc-TIAL1-1,lnc-TIAL1-1:2,lnc-TIAL1-1:3,lnc-TIAL1-1:4 RNACentral:URS0000D5A908,RNACentral:URS00008C3BF0,RNACentral:URS0000D5973A,RNACentral:URS00009B8A32 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119677000..119677233 26863196 MeRIP-seq:(Medium) rs1405717595 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_488 87845 RMVar_ID_87845 Human_SNP_ID_449122756 m1A Human chr10 + 119677147 119677147 119677147 CTGCAGGCAATCATGGAGATGGGTGCCGTGGCAGCAGACAAGGGCAAGAAAAATGCTGGAAATGC CTGCAGGCAATCATGGAGATGGGTGCCGTGGCGGCAGACAAGGGCAAGAAAAATGCTGGAAATGC A G BAG3 Ensembl:ENSG00000151929 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:119676917..119677262 26863196 MeRIP-seq:(Medium) rs1057521271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5936428,Human_RBP_ID_17771324 87846 RMVar_ID_87846 Human_SNP_ID_449122774 m1A Human chr10 + 119677191 119677191 119677191 CAAGAAAAATGCTGGAAATGCAGAAGATCCCCACACAGAAACCCAGCAGCCAGAAGCCACAGCAG CAAGAAAAATGCTGGAAATGCAGAAGATCCCCTCACAGAAACCCAGCAGCCAGAAGCCACAGCAG A T BAG3 Ensembl:ENSG00000151929 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119676457..119677274 26863196 MeRIP-seq:(Medium) rs1334550097 Functional Loss SNV dbSNP153 33..33 33 - - - 87847 RMVar_ID_87847 Human_SNP_ID_449151170 m1A Human chr10 + 119788290 119788290 119788290 CAGTCTTGAGATTAGGGGAAAAGAGTGGAGTTAGCAAAGGTAGTAGTAGTTAAAATTAGGAAAGA CAGTCTTGAGATTAGGGGAAAAGAGTGGAGTTCGCAAAGGTAGTAGTAGTTAAAATTAGGAAAGA A C INPP5F Ensembl:ENSG00000198825 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:119788239..119788374 26863196 MeRIP-seq:(Medium) rs1476060642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9702,RMVar_hsa_circ_325530,RMVar_hsa_circ_49019,RMVar_hsa_circ_146693,RMVar_hsa_circ_146692,RMVar_hsa_circ_337133,RMVar_hsa_circ_24977 87848 RMVar_ID_87848 Human_SNP_ID_449167263 m1A Human chr10 - 119847625 119847625 119847625 ACTGTCTGTGGATCCTGTGCTGAGTATACTGAATAATGATGAAAGGTGAGTCTGTGTGCTCTTTT ACTGTCTGTGGATCCTGTGCTGAGTATACTGATTAATGATGAAAGGTGAGTCTGTGTGCTCTTTT T A MCMBP Ensembl:ENSG00000197771 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs760025991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1076209,Human_RBP_ID_18970436,Human_RBP_ID_22489480,Human_RBP_ID_22878392,Human_RBP_ID_23438956 Human_Splice_Rec_1182104,Human_Splice_Rec_1182105,Human_Splice_Rec_1182132,Human_Splice_Rec_1182133,Human_Splice_Rec_1182162,Human_Splice_Rec_1182163,Human_Splice_Rec_1182182,Human_Splice_Rec_1182183 RMVar_hsa_circ_362178,RMVar_hsa_circ_363649,RMVar_hsa_circ_36202,RMVar_hsa_circ_313876,RMVar_hsa_circ_314087,RMVar_hsa_circ_101208,RMVar_hsa_circ_16674,RMVar_hsa_circ_146710,RMVar_hsa_circ_146711,RMVar_hsa_circ_146712,RMVar_hsa_circ_61897,RMVar_hsa_circ_50459,RMVar_hsa_circ_51236,RMVar_hsa_circ_265043,RMVar_hsa_circ_355269,RMVar_hsa_circ_318578,RMVar_hsa_circ_146715,RMVar_hsa_circ_308860,RMVar_hsa_circ_146716,RMVar_hsa_circ_14337,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718 87849 RMVar_ID_87849 Human_SNP_ID_449170514 m1A Human chr10 - 119859879 119859879 119859879 GCTTTGAAAAGTATATTTCTCTTTCAGCCCAAAATGGAGTTAATCCTGACTGGGAGAAGAAAGTA GCTTTGAAAAGTATATTTCTCTTTCAGCCCAAGATGGAGTTAATCCTGACTGGGAGAAGAAAGTA T C MCMBP Ensembl:ENSG00000197771 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:119859828..119872621 32194978 MeRIP-seq:(Medium) rs750591532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862928 Human_Splice_Rec_1182094,Human_Splice_Rec_1182095,Human_Splice_Rec_1182122,Human_Splice_Rec_1182123,Human_Splice_Rec_1182150,Human_Splice_Rec_1182151,Human_Splice_Rec_1182188,Human_Splice_Rec_1182189 RMVar_hsa_circ_36202,RMVar_hsa_circ_11496,RMVar_hsa_circ_146712,RMVar_hsa_circ_50459,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718,RMVar_hsa_circ_329119,RMVar_hsa_circ_146722 87850 RMVar_ID_87850 Human_SNP_ID_449173970 m1A Human chr10 - 119872792 119872792 119872792 AGGGGCCCGTACGCGCCCGCCTGACTGTCGCCAGCAGCTCCTCGGCGGCCCCACCGCAGCCGCCG AGGGGCCCGTACGCGCCCGCCTGACTGTCGCCGGCAGCTCCTCGGCGGCCCCACCGCAGCCGCCG T C MCMBP Ensembl:ENSG00000197771 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr10:119872526..119872850;chr10:119872601..119872850 26863196 MeRIP-seq:(Medium) rs943429153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226000,Human_RBP_ID_4136072,Human_RBP_ID_5435142,Human_RBP_ID_5459786,Human_RBP_ID_5520326,Human_RBP_ID_9274027,Human_RBP_ID_9320731,Human_RBP_ID_22432277 87851 RMVar_ID_87851 Human_SNP_ID_449179103 m1A Human chr10 - 119892822 119892822 119892822 GAAAAGTAAGTTAGTGCCCGATGAGGAAGTGGAGGCGCCGCCGCTGCCACCGTTAGGTTTTCTCT GAAAAGTAAGTTAGTGCCCGATGAGGAAGTGGCGGCGCCGCCGCTGCCACCGTTAGGTTTTCTCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:119892775..119892863;chr10:119892772..119892895 26863196 MeRIP-seq:(Medium) rs755848243 Functional Loss SNV dbSNP153 33..33 33 - - - 87852 RMVar_ID_87852 Human_SNP_ID_449180756 m1A Human chr10 - 119898726 119898726 119898726 AGGAGGGAGACTACTTGGCTGAGAAGGCAGATAAGAATTTATTCCCATCAGTGAGGAAGGTGGAG AGGAGGGAGACTACTTGGCTGAGAAGGCAGATGAGAATTTATTCCCATCAGTGAGGAAGGTGGAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:119898676..119898807 26863196 MeRIP-seq:(Medium) rs1295304116 Functional Loss SNV dbSNP153 33..33 33 - - - 87853 RMVar_ID_87853 Human_SNP_ID_449180784 m1A Human chr10 + 119898794 119898794 119898794 TATTTTGGGAACCAACCCCAAGGAATTCCCCAACCAGGATACAATCCATATCGCCATACCCCTGG TATTTTGGGAACCAACCCCAAGGAATTCCCCATCCAGGATACAATCCATATCGCCATACCCCTGG A T SEC23IP Ensembl:ENSG00000107651 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:119898679..119898825 26863196 MeRIP-seq:(Medium) rs36060726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17229549,Human_RBP_ID_17342622,Human_RBP_ID_22029974 Human_miRNA_ID_2766721 RMVar_hsa_circ_146725,RMVar_hsa_circ_306868,RMVar_hsa_circ_333640,RMVar_hsa_circ_352817,RMVar_hsa_circ_341509,RMVar_hsa_circ_313077,RMVar_hsa_circ_75225,RMVar_hsa_circ_76406,RMVar_hsa_circ_146727,RMVar_hsa_circ_37546,RMVar_hsa_circ_146726,RMVar_hsa_circ_146724 87854 RMVar_ID_87854 Human_SNP_ID_721205545 m1A Human chrX + 75156242 75156242 75156242 GCGCTTTTCGAAAGCAGCCGCCGCGGCCGCCCAGCGCCAAGAATGCATCGCGAGCAGCGCCATCT GCGCTTTTCGAAAGCAGCCGCCGCGGCCGCCCGGCGCCAAGAATGCATCGCGAGCAGCGCCATCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:75156162..75156250 26863196 MeRIP-seq:(Medium) rs914493590 Functional Loss SNV dbSNP153 33..33 33 - - - 87855 RMVar_ID_87855 Human_SNP_ID_721347307 m1A Human chrX + 75747119 75747098 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCC_____________________GCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC CGCCGCCGCGGCCGCCGCCGCA C lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs1353821898 Functional Loss DEL dbSNP153 13..33 33 - - - 87856 RMVar_ID_87856 Human_SNP_ID_721347333 m1A Human chrX + 75747119 75747104 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCCGCCGCC_______________GCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC CGCGGCCGCCGCCGCA C lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs1569450066 Functional Loss DEL dbSNP153 19..33 33 - - - 87857 RMVar_ID_87857 Human_SNP_ID_721347364 m1A Human chrX + 75747119 75747113 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCCGCCGCCGCGGCCGCC______GCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC CGCCGCA C lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs1467073140 Functional Loss DEL dbSNP153 28..33 33 - - - 87858 RMVar_ID_87858 Human_SNP_ID_721347377 m1A Human chrX + 75747119 75747119 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCCGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC A C lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs867705200 Functional Loss SNV dbSNP153 33..33 33 - - - 87859 RMVar_ID_87859 Human_SNP_ID_721347378 m1A Human chrX + 75747119 75747119 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCGGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC A G lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs867705200 Functional Loss SNV dbSNP153 33..33 33 - - - 87860 RMVar_ID_87860 Human_SNP_ID_721347379 m1A Human chrX + 75747119 75747119 75747119 GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCAGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC GCCACCGCCGCCGCCGCCGCGGCCGCCGCCGCTGCAGCCGCCGCTGCCGCCGCCGCCGCCGCTGC A T lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:75747038..75747120;chrX:75746987..75747202;chrX:75746996..75747186 26863196 MeRIP-seq:(Medium) rs867705200 Functional Loss SNV dbSNP153 33..33 33 - - - 87861 RMVar_ID_87861 Human_SNP_ID_721867971 m1A Human chrX - 77682006 77682006 77682006 GTTGTGACTCTTCAGAGGATAAAAAGAGTAAGAATGGAGCATATGGTAGAGAGAAGAAAAGGTGC GTTGTGACTCTTCAGAGGATAAAAAGAGTAAGCATGGAGCATATGGTAGAGAGAAGAAAAGGTGC T G ATRX Ensembl:ENSG00000085224 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:77681958..77682089 26863196 MeRIP-seq:(Medium) rs782060288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220784,Human_RBP_ID_3266922,Human_RBP_ID_8938222,Human_RBP_ID_16944068,Human_RBP_ID_23106513,Human_RBP_ID_24354461,Human_RBP_ID_24555737,Human_RBP_ID_26363174 RMVar_hsa_circ_439,RMVar_hsa_circ_28835,RMVar_hsa_circ_320678,RMVar_hsa_circ_71465,RMVar_hsa_circ_12638,RMVar_hsa_circ_43326,RMVar_hsa_circ_348656,RMVar_hsa_circ_358108,RMVar_hsa_circ_352386,RMVar_hsa_circ_66963,RMVar_hsa_circ_72041,RMVar_hsa_circ_330981,RMVar_hsa_circ_276175,RMVar_hsa_circ_306104,RMVar_hsa_circ_13270,RMVar_hsa_circ_355973,RMVar_hsa_circ_281242,RMVar_hsa_circ_108994,RMVar_hsa_circ_263091,RMVar_hsa_circ_263092,RMVar_hsa_circ_263093 87862 RMVar_ID_87862 Human_SNP_ID_721867976 m1A Human chrX - 77682023 77682023 77682023 AACAGGGAAAGGAGATAGTTGTGACTCTTCAGAGGATAAAAAGAGTAAGAATGGAGCATATGGTA AACAGGGAAAGGAGATAGTTGTGACTCTTCAGGGGATAAAAAGAGTAAGAATGGAGCATATGGTA T C ATRX Ensembl:ENSG00000085224 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:77681973..77682110 26863196 MeRIP-seq:(Medium) rs1417955952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8938223,Human_RBP_ID_23106514,Human_RBP_ID_24354461,Human_RBP_ID_26363174 RMVar_hsa_circ_439,RMVar_hsa_circ_28835,RMVar_hsa_circ_320678,RMVar_hsa_circ_71465,RMVar_hsa_circ_12638,RMVar_hsa_circ_43326,RMVar_hsa_circ_348656,RMVar_hsa_circ_358108,RMVar_hsa_circ_352386,RMVar_hsa_circ_66963,RMVar_hsa_circ_72041,RMVar_hsa_circ_330981,RMVar_hsa_circ_276175,RMVar_hsa_circ_306104,RMVar_hsa_circ_13270,RMVar_hsa_circ_355973,RMVar_hsa_circ_281242,RMVar_hsa_circ_108994,RMVar_hsa_circ_263091,RMVar_hsa_circ_263092,RMVar_hsa_circ_263093 87863 RMVar_ID_87863 Human_SNP_ID_721887448 m1A Human chrX + 77786072 77786072 77786072 GGGCGCCGATCTGCGCTCCCCCGCGCCCGGTTACGATAGAAATGCACTGGAGTCTTAGTCGTCAC GGGCGCCGATCTGCGCTCCCCCGCGCCCGGTTGCGATAGAAATGCACTGGAGTCTTAGTCGTCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:77786021..77786225 26863196 MeRIP-seq:(Medium) rs781792933 Functional Loss SNV dbSNP153 33..33 33 - - - 87864 RMVar_ID_87864 Human_SNP_ID_721887464 m1A Human chrX + 77786166 77786166 77786166 TCAAAGGCCGCTACCACTGCCACCGCCGCAGGAGCCGCGGAAACAAAGCGACACCGCTGCCGCCG TCAAAGGCCGCTACCACTGCCACCGCCGCAGGGGCCGCGGAAACAAAGCGACACCGCTGCCGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:77786001..77786225 26863196 MeRIP-seq:(Medium) rs1205071306 Functional Loss SNV dbSNP153 33..33 33 - - - 87865 RMVar_ID_87865 Human_SNP_ID_721908527 m1A Human chrX + 77899525 77899525 77899525 CTGAAGCGAATTGGCACCAAAGCAGCAGCTGTATTGCCGCAGTTCTAGCTTCACCTTCACGATGT CTGAAGCGAATTGGCACCAAAGCAGCAGCTGTGTTGCCGCAGTTCTAGCTTCACCTTCACGATGT A G COX7B Ensembl:ENSG00000131174 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:77899501..77899525 26863196 MeRIP-seq:(Medium) rs782568175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_739776,Human_RBP_ID_1719520,Human_RBP_ID_2079140,Human_RBP_ID_5074369,Human_RBP_ID_8723684,Human_RBP_ID_9339990,Human_RBP_ID_16946352,Human_RBP_ID_17327788,Human_RBP_ID_17442760,Human_RBP_ID_18428052,Human_RBP_ID_18925342,Human_RBP_ID_22349992,Human_RBP_ID_22426785,Human_RBP_ID_22467697,Human_RBP_ID_22520104,Human_RBP_ID_22843354,Human_RBP_ID_26297758,Human_RBP_ID_26573372,Human_RBP_ID_27152014,Human_RBP_ID_27384671 Human_Splice_Rec_2220914,Human_Splice_Rec_2220920,Human_Splice_Rec_2220922,Human_Splice_Rec_2220926 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 87866 RMVar_ID_87866 Human_SNP_ID_721908530 m1A Human chrX + 77899533 77899533 77899533 AATTGGCACCAAAGCAGCAGCTGTATTGCCGCAGTTCTAGCTTCACCTTCACGATGTTTCCCTTG AATTGGCACCAAAGCAGCAGCTGTATTGCCGCGGTTCTAGCTTCACCTTCACGATGTTTCCCTTG A G COX7B Ensembl:ENSG00000131174 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:77899451..77899630;chrX:77899451..77899646 26863196 MeRIP-seq:(Medium) rs11552077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_739776,Human_RBP_ID_1406742,Human_RBP_ID_1719520,Human_RBP_ID_2079141,Human_RBP_ID_5074369,Human_RBP_ID_8723684,Human_RBP_ID_9339990,Human_RBP_ID_17327788,Human_RBP_ID_17442761,Human_RBP_ID_18428052,Human_RBP_ID_18925342,Human_RBP_ID_22349992,Human_RBP_ID_22426785,Human_RBP_ID_22467697,Human_RBP_ID_22520104,Human_RBP_ID_22843354,Human_RBP_ID_26297758,Human_RBP_ID_26573372,Human_RBP_ID_27152014,Human_RBP_ID_27384671 Human_Splice_Rec_2220914,Human_Splice_Rec_2220920,Human_Splice_Rec_2220922,Human_Splice_Rec_2220926 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 87867 RMVar_ID_87867 Human_SNP_ID_721909026 m1A Human chrX - 77902643 77902643 77902643 TCTGCCTTGCCATTGTTTGCTGAATGCTTCGAACTTACAGGAAAACGAAAAAAGAATACAGAAGC TCTGCCTTGCCATTGTTTGCTGAATGCTTCGAGCTTACAGGAAAACGAAAAAAGAATACAGAAGC T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:77902626..77902700 26863196 MeRIP-seq:(Medium) rs781898266 Functional Loss SNV dbSNP153 33..33 33 - - - 87868 RMVar_ID_87868 Human_SNP_ID_721943805 m1A Human chrX + 78104302 78104302 78104302 GGAGCGCACGTCGGCAGTCGGCTCCCTCGTTGACCGAATCACCGACCTCTCTCCCCAGCTGTATT GGAGCGCACGTCGGCAGTCGGCTCCCTCGTTGGCCGAATCACCGACCTCTCTCCCCAGCTGTATT A G PGK1 Ensembl:ENSG00000102144 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:78104226..78104456;chrX:78104226..78104425;chrX:78104226..78104359;chrX:78104226..78104325;chrX:78104251..78104325 26863196 MeRIP-seq:(Medium) rs1557245913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94763,Human_RBP_ID_739834,Human_RBP_ID_1063626,Human_RBP_ID_1232331,Human_RBP_ID_1719543,Human_RBP_ID_2079151,Human_RBP_ID_3929431,Human_RBP_ID_3977564,Human_RBP_ID_5074433,Human_RBP_ID_5272466,Human_RBP_ID_5330514,Human_RBP_ID_5455727,Human_RBP_ID_5483539,Human_RBP_ID_8723721,Human_RBP_ID_8939278,Human_RBP_ID_9265352,Human_RBP_ID_9317572,Human_RBP_ID_9339991,Human_RBP_ID_18428011,Human_RBP_ID_18454758,Human_RBP_ID_18472936,Human_RBP_ID_18925372,Human_RBP_ID_22467992,Human_RBP_ID_22843366,Human_RBP_ID_26834921,Human_RBP_ID_27384688 87869 RMVar_ID_87869 Human_SNP_ID_721943815 m1A Human chrX + 78104314 78104314 78104314 GGCAGTCGGCTCCCTCGTTGACCGAATCACCGACCTCTCTCCCCAGCTGTATTTCCAAAATGTCG GGCAGTCGGCTCCCTCGTTGACCGAATCACCGGCCTCTCTCCCCAGCTGTATTTCCAAAATGTCG A G PGK1 Ensembl:ENSG00000102144 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:78104251..78104461 26863196 MeRIP-seq:(Medium) rs782223094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94763,Human_RBP_ID_739834,Human_RBP_ID_1063626,Human_RBP_ID_1719543,Human_RBP_ID_2079151,Human_RBP_ID_3929431,Human_RBP_ID_3977564,Human_RBP_ID_5074433,Human_RBP_ID_5272466,Human_RBP_ID_5330514,Human_RBP_ID_5432343,Human_RBP_ID_5455727,Human_RBP_ID_5483539,Human_RBP_ID_5518046,Human_RBP_ID_8026941,Human_RBP_ID_8723721,Human_RBP_ID_8938304,Human_RBP_ID_9317573,Human_RBP_ID_17555859,Human_RBP_ID_18428011,Human_RBP_ID_18454758,Human_RBP_ID_18472936,Human_RBP_ID_18925372,Human_RBP_ID_22349996,Human_RBP_ID_22467992,Human_RBP_ID_26834921,Human_RBP_ID_27152027,Human_RBP_ID_27384688,Human_RBP_ID_27553615 Human_Splice_Rec_2221110 87870 RMVar_ID_87870 Human_SNP_ID_721945026 m1A Human chrX - 78109882 78109882 78109882 TGGTTGTTTGTTATCTGGTTGTTCTTCATAGGAACATTGAAGTCGACTCTAAAAAAGAAAGATGC TGGTTGTTTGTTATCTGGTTGTTCTTCATAGGGACATTGAAGTCGACTCTAAAAAAGAAAGATGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:78109851..78109925 26863196 MeRIP-seq:(Medium) rs1569550772 Functional Loss SNV dbSNP153 33..33 33 - - - 87871 RMVar_ID_87871 Human_SNP_ID_721945030 m1A Human chrX + 78109895 78109895 78109895 TTAGAGTCGACTTCAATGTTCCTATGAAGAACAACCAGATAACAAACAACCAGAGGTAAGGTCCC TTAGAGTCGACTTCAATGTTCCTATGAAGAACGACCAGATAACAAACAACCAGAGGTAAGGTCCC A G PGK1 Ensembl:ENSG00000102144 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:78109851..78109925 26863196 MeRIP-seq:(Medium) rs782747270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967442,Human_RBP_ID_1719548,Human_RBP_ID_2079154,Human_RBP_ID_3976729,Human_RBP_ID_5075849,Human_RBP_ID_5535755,Human_RBP_ID_22468408,Human_RBP_ID_24354808,Human_RBP_ID_27553618 Human_Splice_Rec_2221073,Human_Splice_Rec_2221074,Human_Splice_Rec_2221095,Human_Splice_Rec_2221096,Human_Splice_Rec_2221099,Human_Splice_Rec_2221100,Human_Splice_Rec_2221111 RMVar_hsa_circ_27306,RMVar_hsa_circ_117074,RMVar_hsa_circ_375241,RMVar_hsa_circ_98137,RMVar_hsa_circ_263129,RMVar_hsa_circ_263130,RMVar_hsa_circ_263128 87872 RMVar_ID_87872 Human_SNP_ID_721945885 m1A Human chrX + 78114130 78114130 78114130 CTGGAGAACCTCCGCTTTCATGTGGAGGAAGAAGGGAAGGGAAAAGATGCTTCTGGGAACAAGGT CTGGAGAACCTCCGCTTTCATGTGGAGGAAGACGGGAAGGGAAAAGATGCTTCTGGGAACAAGGT A C PGK1 Ensembl:ENSG00000102144 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:78104251..78125157 32194978 MeRIP-seq:(Medium) rs5913638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93522,Human_RBP_ID_799299,Human_RBP_ID_967448,Human_RBP_ID_5074447,Human_RBP_ID_18472937,Human_RBP_ID_22467709 Human_Splice_Rec_2221078,Human_Splice_Rec_2221104,Human_Splice_Rec_2221114 RMVar_hsa_circ_100143,RMVar_hsa_circ_27306,RMVar_hsa_circ_117074,RMVar_hsa_circ_375241,RMVar_hsa_circ_98137,RMVar_hsa_circ_121586,RMVar_hsa_circ_122514,RMVar_hsa_circ_263129,RMVar_hsa_circ_263130,RMVar_hsa_circ_263128,RMVar_hsa_circ_263132,RMVar_hsa_circ_106537,RMVar_hsa_circ_263131,RMVar_hsa_circ_116016,RMVar_hsa_circ_263134,RMVar_hsa_circ_263135,RMVar_hsa_circ_263133 87873 RMVar_ID_87873 Human_SNP_ID_721946445 m1A Human chrX - 78117266 78117266 78117266 CAAAAACAGAAAATGTGATGGCTCCAAAGACAACTATAAAAGCATTTCATACACCAAGAGTCCTC CAAAAACAGAAAATGTGATGGCTCCAAAGACACCTATAAAAGCATTTCATACACCAAGAGTCCTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:78117262..78117457 26863196 MeRIP-seq:(Medium) rs1557247539 Functional Loss SNV dbSNP153 33..33 33 - - - 87874 RMVar_ID_87874 Human_SNP_ID_721946624 m1A Human chrX + 78118116 78118116 78118116 TGGTGGGTTTTTGATGAAGAAGGAGCTGAACTACTTTGCAAAGGCCTTGGAGAGCCCAGAGCGAC TGGTGGGTTTTTGATGAAGAAGGAGCTGAACTGCTTTGCAAAGGCCTTGGAGAGCCCAGAGCGAC A G PGK1 Ensembl:ENSG00000102144 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:78118065..78118220 26863196 MeRIP-seq:(Medium) rs1557247645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93524,Human_RBP_ID_739848,Human_RBP_ID_967453,Human_RBP_ID_1719552,Human_RBP_ID_2079160,Human_RBP_ID_5074456,Human_RBP_ID_8026974,Human_RBP_ID_9265357,Human_RBP_ID_16946826,Human_RBP_ID_18155931,Human_RBP_ID_19027550,Human_RBP_ID_22467715,Human_RBP_ID_22777713,Human_RBP_ID_22843531,Human_RBP_ID_23107655,Human_RBP_ID_26363183,Human_RBP_ID_27152043,Human_RBP_ID_27384699 Human_Splice_Rec_2221081,Human_Splice_Rec_2221082,Human_Splice_Rec_2221107,Human_Splice_Rec_2221108,Human_Splice_Rec_2221117,Human_Splice_Rec_2221118 Human_miRNA_ID_1966907,Human_miRNA_ID_2362364,Human_miRNA_ID_2646213,Human_miRNA_ID_2790606,Human_miRNA_ID_2820230 RMVar_hsa_circ_100143,RMVar_hsa_circ_27306,RMVar_hsa_circ_117074,RMVar_hsa_circ_375241,RMVar_hsa_circ_121586,RMVar_hsa_circ_122514,RMVar_hsa_circ_263129,RMVar_hsa_circ_263130,RMVar_hsa_circ_263132,RMVar_hsa_circ_106537,RMVar_hsa_circ_263131,RMVar_hsa_circ_116016,RMVar_hsa_circ_119614,RMVar_hsa_circ_263134,RMVar_hsa_circ_263135,RMVar_hsa_circ_292523,RMVar_hsa_circ_263133,RMVar_hsa_circ_324471,RMVar_hsa_circ_263136,RMVar_hsa_circ_263138,RMVar_hsa_circ_83016,RMVar_hsa_circ_263137 87875 RMVar_ID_87875 Human_SNP_ID_721948638 m1A Human chrX + 78128312 78128312 78128312 TTACGCCTGTAATCCCAGGACTTTGGGAGGCCAAGGCGGGCAGATCACCTGTCAGGAGTTTGGGA TTACGCCTGTAATCCCAGGACTTTGGGAGGCCGAGGCGGGCAGATCACCTGTCAGGAGTTTGGGA A G PGK1 Ensembl:ENSG00000102144 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2935001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18155938 GWAS_ID_10862,GWAS_ID_10863,GWAS_ID_10864,GWAS_ID_10865,GWAS_ID_10866,GWAS_ID_10867,GWAS_ID_10868,GWAS_ID_10869,GWAS_ID_10870,GWAS_ID_10871,GWAS_ID_10872,GWAS_ID_10873,GWAS_ID_10874,GWAS_ID_10875,GWAS_ID_10876,GWAS_ID_10877,GWAS_ID_10878,GWAS_ID_10879,GWAS_ID_10880,GWAS_ID_10881,GWAS_ID_10882,GWAS_ID_10883,GWAS_ID_10884,GWAS_ID_10885,GWAS_ID_10886,GWAS_ID_10887,GWAS_ID_10888,GWAS_ID_10889,GWAS_ID_10890,GWAS_ID_10891,GWAS_ID_10892,GWAS_ID_10893,GWAS_ID_10894,GWAS_ID_10895,GWAS_ID_10896,GWAS_ID_10897,GWAS_ID_10898,GWAS_ID_10899,GWAS_ID_10900,GWAS_ID_10901,GWAS_ID_10902,GWAS_ID_10903,GWAS_ID_10904 87876 RMVar_ID_87876 Human_SNP_ID_722230336 m1A Human chrX - 79363553 79363553 79363553 TTTGTTTTTGGTTTTGCTTTTTAATAAATAGGAGCTCCGAGTTGCCACCCAGGAAAAAGAGGGCT TTTGTTTTTGGTTTTGCTTTTTAATAAATAGGGGCTCCGAGTTGCCACCCAGGAAAAAGAGGGCT T C ITM2A Ensembl:ENSG00000078596 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:79362959..79363575 32194978 MeRIP-seq:(Medium) rs1360197652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2221221,Human_Splice_Rec_2221239 87877 RMVar_ID_87877 Human_SNP_ID_722516541 m1A Human chrX - 80676957 80676942 80676957 GGAAGATGGGGTAGATGGAGTAGAGGAGGCAGAGGAAGAGGAGGCAGGGGACGAGGGAGTCGAGG GGAAGATGGGGTAGATGGAGTAGAGGAGGCAG_______________GGGACGAGGGAGTCGAGG CCTGCCTCCTCTTCCT C BRWD3 Ensembl:ENSG00000165288 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:80676831..80677092 26863196 MeRIP-seq:(Medium) rs761235446 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_94990,Human_RBP_ID_8027266,Human_RBP_ID_17070889,Human_RBP_ID_26573860 87878 RMVar_ID_87878 Human_SNP_ID_722516544 m1A Human chrX - 80676957 80676957 80676957 GGAAGATGGGGTAGATGGAGTAGAGGAGGCAGAGGAAGAGGAGGCAGGGGACGAGGGAGTCGAGG GGAAGATGGGGTAGATGGAGTAGAGGAGGCAGTGGAAGAGGAGGCAGGGGACGAGGGAGTCGAGG T A BRWD3 Ensembl:ENSG00000165288 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:80676831..80677092 26863196 MeRIP-seq:(Medium) rs1055391282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94990,Human_RBP_ID_8027266,Human_RBP_ID_17070889,Human_RBP_ID_26573860 87879 RMVar_ID_87879 Human_SNP_ID_722516547 m1A Human chrX - 80676966 80676966 80676966 GGCAGATGGGGAAGATGGGGTAGATGGAGTAGAGGAGGCAGAGGAAGAGGAGGCAGGGGACGAGG GGCAGATGGGGAAGATGGGGTAGATGGAGTAGGGGAGGCAGAGGAAGAGGAGGCAGGGGACGAGG T C BRWD3 Ensembl:ENSG00000165288 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:80676831..80677107 26863196 MeRIP-seq:(Medium) rs769966904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8027266 87880 RMVar_ID_87880 Human_SNP_ID_722516548 m1A Human chrX - 80676968 80676968 80676968 GAGGCAGATGGGGAAGATGGGGTAGATGGAGTAGAGGAGGCAGAGGAAGAGGAGGCAGGGGACGA GAGGCAGATGGGGAAGATGGGGTAGATGGAGTGGAGGAGGCAGAGGAAGAGGAGGCAGGGGACGA T C BRWD3 Ensembl:ENSG00000165288 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:80676802..80677056 26863196 MeRIP-seq:(Medium) rs1208029358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5074597,Human_RBP_ID_8027266,Human_RBP_ID_26308938 87881 RMVar_ID_87881 Human_SNP_ID_722604679 m1A Human chrX - 81114931 81114931 81114931 GGTGAAGACGGAAAAGGAAATGGAGAAGATGGAAAAGAGAAAGGAGAAGATGAAAAAGAGGAAGA GGTGAAGACGGAAAAGGAAATGGAGAAGATGGTAAAGAGAAAGGAGAAGATGAAAAAGAGGAAGA T A HMGN5 Ensembl:ENSG00000198157 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:81114626..81116300 26863196 MeRIP-seq:(Medium) rs1227635204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95110,Human_RBP_ID_5074760,Human_RBP_ID_5231333,Human_RBP_ID_24355191 87882 RMVar_ID_87882 Human_SNP_ID_722604686 m1A Human chrX - 81114952 81114952 81114952 GAGAAAGAAGATGGAAAAAAAGGTGAAGACGGAAAAGGAAATGGAGAAGATGGAAAAGAGAAAGG GAGAAAGAAGATGGAAAAAAAGGTGAAGACGGCAAAGGAAATGGAGAAGATGGAAAAGAGAAAGG T G HMGN5 Ensembl:ENSG00000198157 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:81114856..81115016 26863196 MeRIP-seq:(Medium) rs374637006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95110,Human_RBP_ID_8027571,Human_RBP_ID_24355191 87883 RMVar_ID_87883 Human_SNP_ID_723306574 m1A Human chrX + 84188011 84188011 84188011 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGACCCCCAGCCCCGCCTTCAGCGAGCGCTGCCCT CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGCCCCCCAGCCCCGCCTTCAGCGAGCGCTGCCCT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:84187896..84188012 26863196 MeRIP-seq:(Medium) rs1307170618 Functional Loss SNV dbSNP153 33..33 33 - - - 87884 RMVar_ID_87884 Human_SNP_ID_723306575 m1A Human chrX + 84188011 84188011 84188011 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGACCCCCAGCCCCGCCTTCAGCGAGCGCTGCCCT CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGGCCCCCAGCCCCGCCTTCAGCGAGCGCTGCCCT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:84187896..84188012 26863196 MeRIP-seq:(Medium) rs1307170618 Functional Loss SNV dbSNP153 33..33 33 - - - 87885 RMVar_ID_87885 Human_SNP_ID_723510899 m1A Human chrX + 85244123 85244119 85244124 AGAGCGCGGTCACAGTCCGACTGGCGGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGG AGAGCGCGGTCACAGTCCGACTGGCGGCA_____GCGGCGGCGGCGGCGGCGGCGGCAGCGGCGG ACGGAG A ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:85244023..85244145 26863196 MeRIP-seq:(Medium) rs1224815408 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_5074864,Human_RBP_ID_9318304,Human_RBP_ID_21960909,Human_RBP_ID_27797215 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 Human_miRNA_ID_3134425 87886 RMVar_ID_87886 Human_SNP_ID_723510915 m1A Human chrX + 85244148 85244124 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAG________________________GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCGGCGGCGGCGGCGGCGGCGGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs1260835613 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87887 RMVar_ID_87887 Human_SNP_ID_723510917 m1A Human chrX + 85244148 85244127 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCG_____________________GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCGGCGGCGGCGGCGGCGGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs944048283 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87888 RMVar_ID_87888 Human_SNP_ID_723510923 m1A Human chrX + 85244148 85244133 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCGGCGGCG_______________GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCGGCGGCGGCGGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs1281882182 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87889 RMVar_ID_87889 Human_SNP_ID_723510935 m1A Human chrX + 85244148 85244139 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCGGCGGCGGCGGCG_________GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCGGCGGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs1178470769 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87890 RMVar_ID_87890 Human_SNP_ID_723510938 m1A Human chrX + 85244148 85244142 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCGGCGGCGGCGGCGGCG______GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCGGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs1430088851 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87891 RMVar_ID_87891 Human_SNP_ID_723510939 m1A Human chrX + 85244148 85244145 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCGGCGGCGGCGGCGGCGGCG___GCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCA G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs1182624792 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 87892 RMVar_ID_87892 Human_SNP_ID_723510945 m1A Human chrX + 85244148 85244148 85244148 GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC GGCACGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCTGTAGC A G ZNF711 Ensembl:ENSG00000147180 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:85244051..85244225 26863410 MeRIP-seq:(Medium) rs375972814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932153 Human_Splice_Rec_2221923,Human_Splice_Rec_2221939 Clinvar_Rec_489 87893 RMVar_ID_87893 Human_SNP_ID_723510971 m1A Human chrX - 85244177 85244177 85244177 CGTCAGGAGTCTCCTTACCTGCTGCTGCAGCTACAGCTGCCGCCGCCGCTGCCGCCGCCGCTGCC CGTCAGGAGTCTCCTTACCTGCTGCTGCAGCTGCAGCTGCCGCCGCCGCTGCCGCCGCCGCTGCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:85244101..85244225 26863410 MeRIP-seq:(Medium) rs1275844705 Functional Loss SNV dbSNP153 33..33 33 - - - 87894 RMVar_ID_87894 Human_SNP_ID_723516004 m1A Human chrX - 85272992 85272992 85272992 ATATGCATTACATTTATGAACAGGATTTTCATAAAATTTCCCTAAACCAGCTTTTAATATTAAGT ATATGCATTACATTTATGAACAGGATTTTCATGAAATTTCCCTAAACCAGCTTTTAATATTAAGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:85272942..85273060 32194978 MeRIP-seq:(Medium) rs1206245961 Functional Loss SNV dbSNP153 33..33 33 - - - 87895 RMVar_ID_87895 Human_SNP_ID_723656647 m1A Human chrX + 85869471 85869471 85869471 CTGTGGCTGGATCCCACACCACATACTTCCATATATCTTGTCATGCACCACCTGCCTCCTAAGAT CTGTGGCTGGATCCCACACCACATACTTCCATGTATCTTGTCATGCACCACCTGCCTCCTAAGAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:85869420..85869536 26863196 MeRIP-seq:(Medium) rs987999563 Functional Loss SNV dbSNP153 33..33 33 - - - 87896 RMVar_ID_87896 Human_SNP_ID_723664851 m1A Human chrX + 85914585 85914585 85914585 CTCCCCAAGCCACGCTGCCAGGGCCCACATGCATAAGAATCTACCACCACCACATCAGCGCCCAT CTCCCCAAGCCACGCTGCCAGGGCCCACATGCGTAAGAATCTACCACCACCACATCAGCGCCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:85914535..85914627 26863196 MeRIP-seq:(Medium) rs1012814437 Functional Loss SNV dbSNP153 33..33 33 - - - 87897 RMVar_ID_87897 Human_SNP_ID_323112152 m1A Human chr7 + 62402825 62402825 62402825 GGAATGGACTCGAATGGAATGGAATAGAATGGAATCAACATGAGTGCAATGGAATGGAGTGGAAT GGAATGGACTCGAATGGAATGGAATAGAATGGGATCAACATGAGTGCAATGGAATGGAGTGGAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:62402773..62402866 26863196 MeRIP-seq:(Medium) rs915065400 Functional Loss SNV dbSNP153 33..33 33 - - - 87898 RMVar_ID_87898 Human_SNP_ID_323721666 m1A Human chr7 + 64434217 64434217 64434217 CCTCATTCCAGCAGCTAACACTGGCGAGTCCAAAGTTTTCTATTATAAAATGAAAGGGGACTACC CCTCATTCCAGCAGCTAACACTGGCGAGTCCAGAGTTTTCTATTATAAAATGAAAGGGGACTACC A G YWHAEP1 Ensembl:ENSG00000232727 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs528546101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1866163,Human_miRNA_ID_1866371 87899 RMVar_ID_87899 Human_SNP_ID_323781805 m1A Human chr7 + 64680109 64680109 64680109 TCCCTATATCCCTTCTGTCCCTACTCTGCCCCATACCCGAACTGGCTGACAATTTGGTCCCACTT TCCCTATATCCCTTCTGTCCCTACTCTGCCCCGTACCCGAACTGGCTGACAATTTGGTCCCACTT A G ZNF107 Ensembl:ENSG00000196247 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:64679979..64680108 26863196 MeRIP-seq:(Medium) rs1243432055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134517,Human_RBP_ID_16187061,Human_RBP_ID_17092271,Human_RBP_ID_18959260 RMVar_hsa_circ_97353,RMVar_hsa_circ_269333,RMVar_hsa_circ_245265,RMVar_hsa_circ_371910,RMVar_hsa_circ_245266 87900 RMVar_ID_87900 Human_SNP_ID_323824613 m1A Human chr7 - 64838922 64838922 64838922 TCTCCGCCGCCATCTCCTTCTGCACCACTGCCATCTTACTACCTGCTTCCTCACCGCCGCCATCT TCTCCGCCGCCATCTCCTTCTGCACCACTGCCGTCTTACTACCTGCTTCCTCACCGCCGCCATCT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:64838829..64838990 26863196 MeRIP-seq:(Medium) rs191496343 Functional Loss SNV dbSNP153 33..33 33 - - - 87901 RMVar_ID_87901 Human_SNP_ID_323878623 m1A Human chr7 + 65038369 65038369 65038369 TGGAGGCGGAGGGAGGCGGTGGCGGCGGCGGCAGGATGGCGACGGCCGTCCTGCTGAGCGTGTCG TGGAGGCGGAGGGAGGCGGTGGCGGCGGCGGCCGGATGGCGACGGCCGTCCTGCTGAGCGTGTCG A C CCT6P3 Ensembl:ENSG00000234585 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:65038318..65038652 26863196 MeRIP-seq:(Medium) rs1472796365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860560,Human_RBP_ID_4946272,Human_RBP_ID_5403047,Human_RBP_ID_5533885,Human_RBP_ID_8218318,Human_RBP_ID_9439258,Human_RBP_ID_17429467,Human_RBP_ID_18426009,Human_RBP_ID_18466077,Human_RBP_ID_18505442,Human_RBP_ID_22622963 87902 RMVar_ID_87902 Human_SNP_ID_323878668 m1A Human chr7 - 65038471 65038470 65038471 GGGGTCCCGCTCCTTCTGCCTCTCCACATGGTAGGCGTAGATGGAGAGCAGGATTCCGGCAGCGC GGGGTCCCGCTCCTTCTGCCTCTCCACATGGT_GGCGTAGATGGAGAGCAGGATTCCGGCAGCGC CT C lnc-ERV3-1-3 RNACentral:URS00008B76FF lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65038282..65038511 26863196 MeRIP-seq:(Medium) rs1322442013 Functional Loss DEL dbSNP153 33..33 33 - - - 87903 RMVar_ID_87903 Human_SNP_ID_323878669 m1A Human chr7 - 65038471 65038471 65038471 GGGGTCCCGCTCCTTCTGCCTCTCCACATGGTAGGCGTAGATGGAGAGCAGGATTCCGGCAGCGC GGGGTCCCGCTCCTTCTGCCTCTCCACATGGTTGGCGTAGATGGAGAGCAGGATTCCGGCAGCGC T A lnc-ERV3-1-3 RNACentral:URS00008B76FF lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65038282..65038511 26863196 MeRIP-seq:(Medium) rs1435772273 Functional Loss SNV dbSNP153 33..33 33 - - - 87904 RMVar_ID_87904 Human_SNP_ID_323878728 m1A Human chr7 + 65038609 65038609 65038609 TGGGGAGTGGGCCGGGAGCGGCCGAGCGGGGCAAGGGCGGAGTCTCGGGGTGGGGAGCGCGCGGC TGGGGAGTGGGCCGGGAGCGGCCGAGCGGGGCGAGGGCGGAGTCTCGGGGTGGGGAGCGCGCGGC A G CCT6P3 Ensembl:ENSG00000234585 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65038570..65038690 26863196 MeRIP-seq:(Medium) rs907738196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267449,Human_RBP_ID_843098,Human_RBP_ID_3862375,Human_RBP_ID_5404041,Human_RBP_ID_5624039,Human_RBP_ID_5657805,Human_RBP_ID_8218319,Human_RBP_ID_8238086,Human_RBP_ID_17200293,Human_RBP_ID_18959266,Human_RBP_ID_19136455,Human_RBP_ID_26794486 87905 RMVar_ID_87905 Human_SNP_ID_323878816 m1A Human chr7 - 65038856 65038856 65038856 CCTCGCGCTCCTGCCCAGCCCGGCCCCGGCCCACCCGACCGCTCCGCGTCCGCCCCGGCCTCCCG CCTCGCGCTCCTGCCCAGCCCGGCCCCGGCCCGCCCGACCGCTCCGCGTCCGCCCCGGCCTCCCG T C lnc-ERV3-1-3 RNACentral:URS00008B76FF lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65038803..65039042 26863196 MeRIP-seq:(Medium) rs893771128 Functional Loss SNV dbSNP153 33..33 33 - - - 87906 RMVar_ID_87906 Human_SNP_ID_323878829 m1A Human chr7 + 65038886 65038886 65038886 GGTGGGCCGGGGCCGGGCTGGGCAGGAGCGCGAGGGGGCTGCGGAGGGTGGGTGCAGGCTGGCTT GGTGGGCCGGGGCCGGGCTGGGCAGGAGCGCGGGGGGGCTGCGGAGGGTGGGTGCAGGCTGGCTT A G CCT6P3 Ensembl:ENSG00000234585 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:65038810..65039066 26863196 MeRIP-seq:(Medium) rs1202538028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267450,Human_RBP_ID_843099,Human_RBP_ID_3860561,Human_RBP_ID_5090805,Human_RBP_ID_5327858,Human_RBP_ID_5403049,Human_RBP_ID_8149536,Human_RBP_ID_8218321,Human_RBP_ID_8237704,Human_RBP_ID_8730799,Human_RBP_ID_9337162,Human_RBP_ID_9438886,Human_RBP_ID_17170538,Human_RBP_ID_17316479,Human_RBP_ID_17543794,Human_RBP_ID_18959267,Human_RBP_ID_21994565,Human_RBP_ID_22731139,Human_RBP_ID_26772060,Human_RBP_ID_26793545 87907 RMVar_ID_87907 Human_SNP_ID_323884747 m1A Human chr7 - 65062240 65062240 65062240 CCACGAATGATGACAACCTTCCCTTCCTGCCAACCCCCATCTTGTCCTCCCAATTCTAAGACACC CCACGAATGATGACAACCTTCCCTTCCTGCCAGCCCCCATCTTGTCCTCCCAATTCTAAGACACC T C lnc-ERV3-1-3,lnc-ERV3-1-1 RNACentral:URS00008B76FF,RNACentral:URS00008C0E81 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:65062189..65062412 26863196 MeRIP-seq:(Medium) rs1253685561 Functional Loss SNV dbSNP153 33..33 33 - - - 87908 RMVar_ID_87908 Human_SNP_ID_323887303 m1A Human chr7 + 65073813 65073813 65073813 TGATTGCCACCAACATTCTCTTGGTTGATGAGATCATGCGAGCTGGAATGTCTTCTCTGAAAGGT TGATTGCCACCAACATTCTCTTGGTTGATGAGCTCATGCGAGCTGGAATGTCTTCTCTGAAAGGT A C CCT6P3 Ensembl:ENSG00000234585 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs561055417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429506 Human_Splice_Rec_870200,Human_Splice_Rec_870220,Human_Splice_Rec_870242 Human_miRNA_ID_1862647,Human_miRNA_ID_1899307,Human_miRNA_ID_2480837,Human_miRNA_ID_2480838,Human_miRNA_ID_2951724,Human_miRNA_ID_2951725 RMVar_hsa_circ_120185,RMVar_hsa_circ_245283 87909 RMVar_ID_87909 Human_SNP_ID_323898075 m1A Human chr7 + 65113154 65113154 65113154 AAAAGGAGGGAGGGAGGAAAGGAGAAAAGGAAAGAAAACAAGAAAGTGAGAAAGAAAGAATAAGA AAAAGGAGGGAGGGAGGAAAGGAGAAAAGGAAGGAAAACAAGAAAGTGAGAAAGAAAGAATAAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65113074..65113230 26863196 MeRIP-seq:(Medium) rs63749631 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_10905,GWAS_ID_10906 87910 RMVar_ID_87910 Human_SNP_ID_324042540 m1A Human chr7 - 65722457 65722457 65722457 CAACTGTGGGGTGACTGCTCCCCCTGGTGGCCATATATGGCTAAAGCAAGTAGAAGTCCAGACAC CAACTGTGGGGTGACTGCTCCCCCTGGTGGCCTTATATGGCTAAAGCAAGTAGAAGTCCAGACAC T A AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:65722413..65722491 32194978 MeRIP-seq:(Medium) rs1449169493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624178 87911 RMVar_ID_87911 Human_SNP_ID_324049912 m1A Human chr7 + 65751170 65751170 65751170 AGTTATGGCGGCGGCGAAGACCCTGAACCCCAAGGCCAAGGTGGCCGGAGCGCAGGCGGCGCTGG AGTTATGGCGGCGGCGAAGACCCTGAACCCCAGGGCCAAGGTGGCCGGAGCGCAGGCGGCGCTGG A G CCT6P1 Ensembl:ENSG00000228409 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:65751119..65751208 26863196 MeRIP-seq:(Medium) rs1234116060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624273,Human_RBP_ID_16192333,Human_RBP_ID_18426012,Human_RBP_ID_22111739 87912 RMVar_ID_87912 Human_SNP_ID_324081932 m1A Human chr7 - 65873284 65873248 65873284 CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCACCGCCGCCTCCGCCGCCGCCGCCACCACCGCC CGTCGGGGCCCGACCCAGCCGCCACCGCCGCC_________________________________ CGGCGGCGGTGGTGGCGGCGGCGGCGGAGGCGGCGGT C RF00017-4501,RF00017-4499 RNACentral:URS000097CADF,RNACentral:URS000098B860 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr7:65873180..65948672;chr7:65873152..65873613;chr7:65873146..65873300;chr7:65873177..65873377 26863196 MeRIP-seq:(Medium) rs1417896074 Functional Loss DEL dbSNP153 33..65 33 - - - 87913 RMVar_ID_87913 Human_SNP_ID_324081956 m1A Human chr7 - 65873284 65873266 65873284 CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCACCGCCGCCTCCGCCGCCGCCGCCACCACCGCC CGTCGGGGCCCGACCCAGCCGCCACCGCCGCC__________________GCCGCCACCACCGCC CGGCGGCGGAGGCGGCGGT C RF00017-4501,RF00017-4499 RNACentral:URS000097CADF,RNACentral:URS000098B860 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr7:65873180..65948672;chr7:65873152..65873613;chr7:65873146..65873300;chr7:65873177..65873377 26863196 MeRIP-seq:(Medium) rs960535374 Functional Loss DEL dbSNP153 33..50 33 - - - 87914 RMVar_ID_87914 Human_SNP_ID_324081983 m1A Human chr7 - 65873284 65873284 65873284 CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCACCGCCGCCTCCGCCGCCGCCGCCACCACCGCC CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCTCCGCCGCCTCCGCCGCCGCCGCCACCACCGCC T A RF00017-4501,RF00017-4499 RNACentral:URS000097CADF,RNACentral:URS000098B860 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr7:65873180..65948672;chr7:65873152..65873613;chr7:65873146..65873300;chr7:65873177..65873377 26863196 MeRIP-seq:(Medium) rs371974807 Functional Loss SNV dbSNP153 33..33 33 - - - 87915 RMVar_ID_87915 Human_SNP_ID_324081984 m1A Human chr7 - 65873284 65873284 65873284 CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCACCGCCGCCTCCGCCGCCGCCGCCACCACCGCC CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCGCCGCCGCCTCCGCCGCCGCCGCCACCACCGCC T C RF00017-4501,RF00017-4499 RNACentral:URS000097CADF,RNACentral:URS000098B860 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr7:65873180..65948672;chr7:65873152..65873613;chr7:65873146..65873300;chr7:65873177..65873377 26863196 MeRIP-seq:(Medium) rs371974807 Functional Loss SNV dbSNP153 33..33 33 - - - 87916 RMVar_ID_87916 Human_SNP_ID_324081985 m1A Human chr7 - 65873284 65873284 65873284 CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCACCGCCGCCTCCGCCGCCGCCGCCACCACCGCC CGTCGGGGCCCGACCCAGCCGCCACCGCCGCCCCCGCCGCCTCCGCCGCCGCCGCCACCACCGCC T G RF00017-4501,RF00017-4499 RNACentral:URS000097CADF,RNACentral:URS000098B860 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr7:65873180..65948672;chr7:65873152..65873613;chr7:65873146..65873300;chr7:65873177..65873377 26863196 MeRIP-seq:(Medium) rs371974807 Functional Loss SNV dbSNP153 33..33 33 - - - 87917 RMVar_ID_87917 Human_SNP_ID_324082023 m1A Human chr7 + 65873343 65873343 65873343 CCGACGGGCGGCGGCGGCTGAGGTGGAGGCGGAGGGAGGCGGCGGCGGCGGCGGCGGGAAGATGG CCGACGGGCGGCGGCGGCTGAGGTGGAGGCGGCGGGAGGCGGCGGCGGCGGCGGCGGGAAGATGG A C VKORC1L1 Ensembl:ENSG00000196715 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr7:65873262..65873417;chr7:65873226..65873467 26863410 MeRIP-seq:(Medium) rs1331224550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794551,Human_RBP_ID_3862380,Human_RBP_ID_4946478,Human_RBP_ID_5327860,Human_RBP_ID_8218324,Human_RBP_ID_8237705,Human_RBP_ID_8914394,Human_RBP_ID_8944162,Human_RBP_ID_9337163,Human_RBP_ID_17672184,Human_RBP_ID_18426013,Human_RBP_ID_26793806 87918 RMVar_ID_87918 Human_SNP_ID_324107018 m1A Human chr7 + 65974385 65974383 65974386 TCACGACCGCGGGGTGGTTCTTGTCCCTACGCACCACTTCTTCCATCACCTGCATGTGGTGATGC TCACGACCGCGGGGTGGTTCTTGTCCCTACG___CACTTCTTCCATCACCTGCATGTGGTGATGC GCAC G lnc-VKORC1L1-2,RF00017-4520,RF00017-4552 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:65974335..65974436 32194978 MeRIP-seq:(Medium) rs768543128 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_118631,RMVar_hsa_circ_245295 87919 RMVar_ID_87919 Human_SNP_ID_324107449 m1A Human chr7 - 65975657 65975657 65975657 TTGTAGCCTGGGCAGAGTGACTCATGCCTGTAATCTCAGCATTTTGGGAGGCTGAGGTGGGTGGA TTGTAGCCTGGGCAGAGTGACTCATGCCTGTACTCTCAGCATTTTGGGAGGCTGAGGTGGGTGGA T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1322432488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_348911,RMVar_hsa_circ_245302,RMVar_hsa_circ_109676,RMVar_hsa_circ_245308,RMVar_hsa_circ_285501,RMVar_hsa_circ_85572,RMVar_hsa_circ_245304,RMVar_hsa_circ_119821,RMVar_hsa_circ_280932,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_245311 87920 RMVar_ID_87920 Human_SNP_ID_324108846 m1A Human chr7 + 65979898 65979898 65979898 GGAGGTAGCCCCCCTCATGCTCTAGCGTGTCGACCCCATTCACCCACTGCAGACACAGGAGATAC GGAGGTAGCCCCCCTCATGCTCTAGCGTGTCGGCCCCATTCACCCACTGCAGACACAGGAGATAC A G lnc-VKORC1L1-2,RF00017-4520,RF00017-4552 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:65979848..65980792 32194978 MeRIP-seq:(Medium) rs928572623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118631,RMVar_hsa_circ_245295 87921 RMVar_ID_87921 Human_SNP_ID_324109603 m1A Human chr7 - 65982074 65982074 65982074 GATGCTGTACCCCCAGGAGAGCCCGTCGCGGGAGTGCAAGGAGCTGGACGGCCTCTGGAGCTTCC GATGCTGTACCCCCAGGAGAGCCCGTCGCGGGTGTGCAAGGAGCTGGACGGCCTCTGGAGCTTCC T A GUSB Ensembl:ENSG00000169919 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:65981962..65982164 32194978 MeRIP-seq:(Medium) rs910537902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957458,Human_RBP_ID_4955798,Human_RBP_ID_9337798,Human_RBP_ID_17169192,Human_RBP_ID_18426330,Human_RBP_ID_22464014,Human_RBP_ID_23080650,Human_RBP_ID_27842898 RMVar_hsa_circ_77148,RMVar_hsa_circ_245313 87922 RMVar_ID_87922 Human_SNP_ID_324109656 m1A Human chr7 + 65982171 65982171 65982171 CAACGGCCCGAGCGCCGCCCAGGCAACCGCCGACCCCCGGGCCATGCTTCCCGGTCCCCCGCTCG CAACGGCCCGAGCGCCGCCCAGGCAACCGCCGGCCCCCGGGCCATGCTTCCCGGTCCCCCGCTCG A G lnc-VKORC1L1-2,RF00017-4520,RF00017-4552 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:65981939..65982225 26863196 MeRIP-seq:(Medium) rs190496263 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_490 RMVar_hsa_circ_118631,RMVar_hsa_circ_245295 87923 RMVar_ID_87923 Human_SNP_ID_324109673 m1A Human chr7 - 65982183 65982183 65982183 GCAGACGGTGGCCGAGCGGGGGACCGGGAAGCATGGCCCGGGGGTCGGCGGTTGCCTGGGCGGCG GCAGACGGTGGCCGAGCGGGGGACCGGGAAGCCTGGCCCGGGGGTCGGCGGTTGCCTGGGCGGCG T G GUSB Ensembl:ENSG00000169919 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:65981976..65982225 26863196 MeRIP-seq:(Medium) rs1382654122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253742,Human_RBP_ID_793904,Human_RBP_ID_843389,Human_RBP_ID_4946678,Human_RBP_ID_9337164,Human_RBP_ID_17166851,Human_RBP_ID_18426332,Human_RBP_ID_22464499 RMVar_hsa_circ_77148,RMVar_hsa_circ_245313 87924 RMVar_ID_87924 Human_SNP_ID_324136212 m1A Human chr7 + 66087351 66087351 66087351 TCCCTGTCCCTGCAGTGGGGCCATTGCAGGCAATCCCCTGGGTGTGGACCGAGAGCTGCTCCGAG TCCCTGTCCCTGCAGTGGGGCCATTGCAGGCAGTCCCCTGGGTGTGGACCGAGAGCTGCTCCGAG A G ASL Ensembl:ENSG00000126522 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:66087346..66088868 32194978 MeRIP-seq:(Medium) rs763948849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954470,Human_RBP_ID_5403060,Human_RBP_ID_24221603,Human_RBP_ID_26356485 Human_Splice_Rec_870682,Human_Splice_Rec_870683,Human_Splice_Rec_870710,Human_Splice_Rec_870711,Human_Splice_Rec_870798,Human_Splice_Rec_870799,Human_Splice_Rec_870826,Human_Splice_Rec_870827,Human_Splice_Rec_870876,Human_Splice_Rec_870877,Human_Splice_Rec_870904,Human_Splice_Rec_870905,Human_Splice_Rec_870928,Human_Splice_Rec_870929,Human_Splice_Rec_870950,Human_Splice_Rec_870960,Human_Splice_Rec_870961 RMVar_hsa_circ_33843,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245323,RMVar_hsa_circ_118242,RMVar_hsa_circ_61514,RMVar_hsa_circ_350597,RMVar_hsa_circ_360166,RMVar_hsa_circ_342396,RMVar_hsa_circ_120280,RMVar_hsa_circ_245324 87925 RMVar_ID_87925 Human_SNP_ID_324154488 m1A Human chr7 + 66154255 66154255 66154255 AGGAGTGCAGTGGCACGATCTCTGCTCACTGCAACCTCTGCCTCCCAGATTCAAGCGATTCTGGT AGGAGTGCAGTGGCACGATCTCTGCTCACTGCGACCTCTGCCTCCCAGATTCAAGCGATTCTGGT A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1129542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26551346 87926 RMVar_ID_87926 Human_SNP_ID_324167988 m1A Human chr7 + 66210068 66210068 66210068 AAGACTAGGTGCACAAAGACCAATAGGTGGTCATTATAGGAATGTAGGTGAAAGATAATGAGGCC AAGACTAGGTGCACAAAGACCAATAGGTGGTCCTTATAGGAATGTAGGTGAAAGATAATGAGGCC A C TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66210063..66210152 26863196 MeRIP-seq:(Medium) rs1036816737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105457,RMVar_hsa_circ_245336 87927 RMVar_ID_87927 Human_SNP_ID_324167989 m1A Human chr7 + 66210068 66210068 66210068 AAGACTAGGTGCACAAAGACCAATAGGTGGTCATTATAGGAATGTAGGTGAAAGATAATGAGGCC AAGACTAGGTGCACAAAGACCAATAGGTGGTCGTTATAGGAATGTAGGTGAAAGATAATGAGGCC A G TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66210063..66210152 26863196 MeRIP-seq:(Medium) rs1036816737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105457,RMVar_hsa_circ_245336 87928 RMVar_ID_87928 Human_SNP_ID_324170993 m1A Human chr7 - 66222607 66222607 66222607 CTTTCTCTCTTTTACACATATCTCCTCAGTCAACCTGTCCCTGACTGCCTTTTTTCGTCTTTCCT CTTTCTCTCTTTTACACATATCTCCTCAGTCATCCTGTCCCTGACTGCCTTTTTTCGTCTTTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66222592..66222659 26863196 MeRIP-seq:(Medium) rs1043083718 Functional Loss SNV dbSNP153 33..33 33 - - - 87929 RMVar_ID_87929 Human_SNP_ID_324170994 m1A Human chr7 - 66222607 66222607 66222607 CTTTCTCTCTTTTACACATATCTCCTCAGTCAACCTGTCCCTGACTGCCTTTTTTCGTCTTTCCT CTTTCTCTCTTTTACACATATCTCCTCAGTCAGCCTGTCCCTGACTGCCTTTTTTCGTCTTTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66222592..66222659 26863196 MeRIP-seq:(Medium) rs1043083718 Functional Loss SNV dbSNP153 33..33 33 - - - 87930 RMVar_ID_87930 Human_SNP_ID_324206221 m1A Human chr7 - 66376677 66376677 66376677 TCGCCTCCCCTCACCTTGCCTCACCTCGCAGCAGCCTTTCCAGGCCCAGCTCCCGCCTCCCGGCG TCGCCTCCCCTCACCTTGCCTCACCTCGCAGCGGCCTTTCCAGGCCCAGCTCCCGCCTCCCGGCG T C LINC00174 Ensembl:ENSG00000179406 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:66376587..66376703 26863196 MeRIP-seq:(Medium) rs1025846881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22110797 87931 RMVar_ID_87931 Human_SNP_ID_324209024 m1A Human chr7 - 66385783 66385783 66385783 GTGTGTCTGAGGCTCTGGAAGGAGGCCAGTGGAGCAGGAGAGAGGGAGAGAATTAGGGCAGTAGG GTGTGTCTGAGGCTCTGGAAGGAGGCCAGTGGGGCAGGAGAGAGGGAGAGAATTAGGGCAGTAGG T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66385733..66385875 26863196 MeRIP-seq:(Medium) rs1189216196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843131,Human_RBP_ID_3867133,Human_RBP_ID_8220544 RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 87932 RMVar_ID_87932 Human_SNP_ID_324218816 m1A Human chr7 - 66423483 66423483 66423483 AAGGGGAAAACTCCTGAGGAGATTCGCAAGACATTCAATATCAAAAATGACTTTACTGAAGAGGA AAGGGGAAAACTCCTGAGGAGATTCGCAAGACTTTCAATATCAAAAATGACTTTACTGAAGAGGA T A SKP1P1,LINC00174 Ensembl:ENSG00000231234,Ensembl:ENSG00000179406 Pseudogene,lincRNA exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6947339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1873056 Clinvar_Rec_491,Clinvar_Rec_492,Clinvar_Rec_493,Clinvar_Rec_4319,Clinvar_Rec_4320,Clinvar_Rec_4321 GWAS_ID_10907,GWAS_ID_10908,GWAS_ID_10909,GWAS_ID_10910,GWAS_ID_10911,GWAS_ID_10912,GWAS_ID_10913,GWAS_ID_10914,GWAS_ID_10915,GWAS_ID_10916,GWAS_ID_10917,GWAS_ID_10918,GWAS_ID_10919,GWAS_ID_10920,GWAS_ID_10921,GWAS_ID_10922,GWAS_ID_10923,GWAS_ID_10924,GWAS_ID_10925,GWAS_ID_10926,GWAS_ID_10927,GWAS_ID_10928,GWAS_ID_10929,GWAS_ID_10930,GWAS_ID_10931,GWAS_ID_10932,GWAS_ID_10933,GWAS_ID_10934,GWAS_ID_10935,GWAS_ID_10936,GWAS_ID_10937,GWAS_ID_10938,GWAS_ID_10939,GWAS_ID_10940,GWAS_ID_10941,GWAS_ID_10942,GWAS_ID_10943,GWAS_ID_10944,GWAS_ID_10945,GWAS_ID_10946,GWAS_ID_10947,GWAS_ID_10948,GWAS_ID_10949,GWAS_ID_10950,GWAS_ID_10951,GWAS_ID_10952,GWAS_ID_10953,GWAS_ID_10954,GWAS_ID_10955,GWAS_ID_10956,GWAS_ID_10957,GWAS_ID_10958,GWAS_ID_10959,GWAS_ID_10960,GWAS_ID_10961,GWAS_ID_10962,GWAS_ID_10963,GWAS_ID_10964,GWAS_ID_10965,GWAS_ID_10966,GWAS_ID_10967,GWAS_ID_10968,GWAS_ID_10969,GWAS_ID_10970,GWAS_ID_10971,GWAS_ID_10972,GWAS_ID_10973,GWAS_ID_10974,GWAS_ID_10975,GWAS_ID_10976,GWAS_ID_10977,GWAS_ID_10978,GWAS_ID_10979,GWAS_ID_10980,GWAS_ID_10981,GWAS_ID_10982,GWAS_ID_10983,GWAS_ID_10984,GWAS_ID_10985,GWAS_ID_10986,GWAS_ID_10987,GWAS_ID_10988,GWAS_ID_10989,GWAS_ID_10990,GWAS_ID_10991,GWAS_ID_10992,GWAS_ID_10993,GWAS_ID_10994,GWAS_ID_10995,GWAS_ID_10996,GWAS_ID_10997,GWAS_ID_10998,GWAS_ID_10999,GWAS_ID_11000,GWAS_ID_11001,GWAS_ID_11002,GWAS_ID_11003,GWAS_ID_11004,GWAS_ID_11005,GWAS_ID_11006,GWAS_ID_11007,GWAS_ID_11008,GWAS_ID_11009,GWAS_ID_11010,GWAS_ID_11011,GWAS_ID_11012,GWAS_ID_11013,GWAS_ID_11014,GWAS_ID_11015,GWAS_ID_11016,GWAS_ID_11017,GWAS_ID_11018,GWAS_ID_11019,GWAS_ID_11020,GWAS_ID_11021,GWAS_ID_11022,GWAS_ID_11023,GWAS_ID_11024,GWAS_ID_11025,GWAS_ID_11026,GWAS_ID_11027 RMVar_hsa_circ_294985,RMVar_hsa_circ_19737,RMVar_hsa_circ_14245,RMVar_hsa_circ_23655,RMVar_hsa_circ_357908,RMVar_hsa_circ_359519,RMVar_hsa_circ_334088,RMVar_hsa_circ_307681,RMVar_hsa_circ_361020,RMVar_hsa_circ_355274,RMVar_hsa_circ_312481,RMVar_hsa_circ_41922,RMVar_hsa_circ_55341,RMVar_hsa_circ_343195,RMVar_hsa_circ_367505,RMVar_hsa_circ_14118,RMVar_hsa_circ_46127,RMVar_hsa_circ_320777,RMVar_hsa_circ_324009,RMVar_hsa_circ_364029,RMVar_hsa_circ_292333,RMVar_hsa_circ_25431 87933 RMVar_ID_87933 Human_SNP_ID_324218817 m1A Human chr7 - 66423483 66423483 66423483 AAGGGGAAAACTCCTGAGGAGATTCGCAAGACATTCAATATCAAAAATGACTTTACTGAAGAGGA AAGGGGAAAACTCCTGAGGAGATTCGCAAGACGTTCAATATCAAAAATGACTTTACTGAAGAGGA T C SKP1P1,LINC00174 Ensembl:ENSG00000231234,Ensembl:ENSG00000179406 Pseudogene,lincRNA exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6947339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1873056 Clinvar_Rec_491,Clinvar_Rec_492,Clinvar_Rec_493,Clinvar_Rec_4319,Clinvar_Rec_4320,Clinvar_Rec_4321 GWAS_ID_10907,GWAS_ID_10908,GWAS_ID_10909,GWAS_ID_10910,GWAS_ID_10911,GWAS_ID_10912,GWAS_ID_10913,GWAS_ID_10914,GWAS_ID_10915,GWAS_ID_10916,GWAS_ID_10917,GWAS_ID_10918,GWAS_ID_10919,GWAS_ID_10920,GWAS_ID_10921,GWAS_ID_10922,GWAS_ID_10923,GWAS_ID_10924,GWAS_ID_10925,GWAS_ID_10926,GWAS_ID_10927,GWAS_ID_10928,GWAS_ID_10929,GWAS_ID_10930,GWAS_ID_10931,GWAS_ID_10932,GWAS_ID_10933,GWAS_ID_10934,GWAS_ID_10935,GWAS_ID_10936,GWAS_ID_10937,GWAS_ID_10938,GWAS_ID_10939,GWAS_ID_10940,GWAS_ID_10941,GWAS_ID_10942,GWAS_ID_10943,GWAS_ID_10944,GWAS_ID_10945,GWAS_ID_10946,GWAS_ID_10947,GWAS_ID_10948,GWAS_ID_10949,GWAS_ID_10950,GWAS_ID_10951,GWAS_ID_10952,GWAS_ID_10953,GWAS_ID_10954,GWAS_ID_10955,GWAS_ID_10956,GWAS_ID_10957,GWAS_ID_10958,GWAS_ID_10959,GWAS_ID_10960,GWAS_ID_10961,GWAS_ID_10962,GWAS_ID_10963,GWAS_ID_10964,GWAS_ID_10965,GWAS_ID_10966,GWAS_ID_10967,GWAS_ID_10968,GWAS_ID_10969,GWAS_ID_10970,GWAS_ID_10971,GWAS_ID_10972,GWAS_ID_10973,GWAS_ID_10974,GWAS_ID_10975,GWAS_ID_10976,GWAS_ID_10977,GWAS_ID_10978,GWAS_ID_10979,GWAS_ID_10980,GWAS_ID_10981,GWAS_ID_10982,GWAS_ID_10983,GWAS_ID_10984,GWAS_ID_10985,GWAS_ID_10986,GWAS_ID_10987,GWAS_ID_10988,GWAS_ID_10989,GWAS_ID_10990,GWAS_ID_10991,GWAS_ID_10992,GWAS_ID_10993,GWAS_ID_10994,GWAS_ID_10995,GWAS_ID_10996,GWAS_ID_10997,GWAS_ID_10998,GWAS_ID_10999,GWAS_ID_11000,GWAS_ID_11001,GWAS_ID_11002,GWAS_ID_11003,GWAS_ID_11004,GWAS_ID_11005,GWAS_ID_11006,GWAS_ID_11007,GWAS_ID_11008,GWAS_ID_11009,GWAS_ID_11010,GWAS_ID_11011,GWAS_ID_11012,GWAS_ID_11013,GWAS_ID_11014,GWAS_ID_11015,GWAS_ID_11016,GWAS_ID_11017,GWAS_ID_11018,GWAS_ID_11019,GWAS_ID_11020,GWAS_ID_11021,GWAS_ID_11022,GWAS_ID_11023,GWAS_ID_11024,GWAS_ID_11025,GWAS_ID_11026,GWAS_ID_11027 RMVar_hsa_circ_294985,RMVar_hsa_circ_19737,RMVar_hsa_circ_14245,RMVar_hsa_circ_23655,RMVar_hsa_circ_357908,RMVar_hsa_circ_359519,RMVar_hsa_circ_334088,RMVar_hsa_circ_307681,RMVar_hsa_circ_361020,RMVar_hsa_circ_355274,RMVar_hsa_circ_312481,RMVar_hsa_circ_41922,RMVar_hsa_circ_55341,RMVar_hsa_circ_343195,RMVar_hsa_circ_367505,RMVar_hsa_circ_14118,RMVar_hsa_circ_46127,RMVar_hsa_circ_320777,RMVar_hsa_circ_324009,RMVar_hsa_circ_364029,RMVar_hsa_circ_292333,RMVar_hsa_circ_25431 87934 RMVar_ID_87934 Human_SNP_ID_324218818 m1A Human chr7 - 66423483 66423483 66423483 AAGGGGAAAACTCCTGAGGAGATTCGCAAGACATTCAATATCAAAAATGACTTTACTGAAGAGGA AAGGGGAAAACTCCTGAGGAGATTCGCAAGACCTTCAATATCAAAAATGACTTTACTGAAGAGGA T G SKP1P1,LINC00174 Ensembl:ENSG00000231234,Ensembl:ENSG00000179406 Pseudogene,lincRNA exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6947339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1873056 Clinvar_Rec_491,Clinvar_Rec_492,Clinvar_Rec_493,Clinvar_Rec_4319,Clinvar_Rec_4320,Clinvar_Rec_4321 GWAS_ID_10907,GWAS_ID_10908,GWAS_ID_10909,GWAS_ID_10910,GWAS_ID_10911,GWAS_ID_10912,GWAS_ID_10913,GWAS_ID_10914,GWAS_ID_10915,GWAS_ID_10916,GWAS_ID_10917,GWAS_ID_10918,GWAS_ID_10919,GWAS_ID_10920,GWAS_ID_10921,GWAS_ID_10922,GWAS_ID_10923,GWAS_ID_10924,GWAS_ID_10925,GWAS_ID_10926,GWAS_ID_10927,GWAS_ID_10928,GWAS_ID_10929,GWAS_ID_10930,GWAS_ID_10931,GWAS_ID_10932,GWAS_ID_10933,GWAS_ID_10934,GWAS_ID_10935,GWAS_ID_10936,GWAS_ID_10937,GWAS_ID_10938,GWAS_ID_10939,GWAS_ID_10940,GWAS_ID_10941,GWAS_ID_10942,GWAS_ID_10943,GWAS_ID_10944,GWAS_ID_10945,GWAS_ID_10946,GWAS_ID_10947,GWAS_ID_10948,GWAS_ID_10949,GWAS_ID_10950,GWAS_ID_10951,GWAS_ID_10952,GWAS_ID_10953,GWAS_ID_10954,GWAS_ID_10955,GWAS_ID_10956,GWAS_ID_10957,GWAS_ID_10958,GWAS_ID_10959,GWAS_ID_10960,GWAS_ID_10961,GWAS_ID_10962,GWAS_ID_10963,GWAS_ID_10964,GWAS_ID_10965,GWAS_ID_10966,GWAS_ID_10967,GWAS_ID_10968,GWAS_ID_10969,GWAS_ID_10970,GWAS_ID_10971,GWAS_ID_10972,GWAS_ID_10973,GWAS_ID_10974,GWAS_ID_10975,GWAS_ID_10976,GWAS_ID_10977,GWAS_ID_10978,GWAS_ID_10979,GWAS_ID_10980,GWAS_ID_10981,GWAS_ID_10982,GWAS_ID_10983,GWAS_ID_10984,GWAS_ID_10985,GWAS_ID_10986,GWAS_ID_10987,GWAS_ID_10988,GWAS_ID_10989,GWAS_ID_10990,GWAS_ID_10991,GWAS_ID_10992,GWAS_ID_10993,GWAS_ID_10994,GWAS_ID_10995,GWAS_ID_10996,GWAS_ID_10997,GWAS_ID_10998,GWAS_ID_10999,GWAS_ID_11000,GWAS_ID_11001,GWAS_ID_11002,GWAS_ID_11003,GWAS_ID_11004,GWAS_ID_11005,GWAS_ID_11006,GWAS_ID_11007,GWAS_ID_11008,GWAS_ID_11009,GWAS_ID_11010,GWAS_ID_11011,GWAS_ID_11012,GWAS_ID_11013,GWAS_ID_11014,GWAS_ID_11015,GWAS_ID_11016,GWAS_ID_11017,GWAS_ID_11018,GWAS_ID_11019,GWAS_ID_11020,GWAS_ID_11021,GWAS_ID_11022,GWAS_ID_11023,GWAS_ID_11024,GWAS_ID_11025,GWAS_ID_11026,GWAS_ID_11027 RMVar_hsa_circ_294985,RMVar_hsa_circ_19737,RMVar_hsa_circ_14245,RMVar_hsa_circ_23655,RMVar_hsa_circ_357908,RMVar_hsa_circ_359519,RMVar_hsa_circ_334088,RMVar_hsa_circ_307681,RMVar_hsa_circ_361020,RMVar_hsa_circ_355274,RMVar_hsa_circ_312481,RMVar_hsa_circ_41922,RMVar_hsa_circ_55341,RMVar_hsa_circ_343195,RMVar_hsa_circ_367505,RMVar_hsa_circ_14118,RMVar_hsa_circ_46127,RMVar_hsa_circ_320777,RMVar_hsa_circ_324009,RMVar_hsa_circ_364029,RMVar_hsa_circ_292333,RMVar_hsa_circ_25431 87935 RMVar_ID_87935 Human_SNP_ID_324245987 m1A Human chr7 + 66531543 66531543 66531543 CCCGCCACCAGCTCCCTGCAGCTCCTCCCTGCATATGGGCCCAGCTGCCCCTCTCCAGCTCCCTT CCCGCCACCAGCTCCCTGCAGCTCCTCCCTGCGTATGGGCCCAGCTGCCCCTCTCCAGCTCCCTT A G AC008267.3 Ensembl:ENSG00000234500 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:66531492..66531655 26863196 MeRIP-seq:(Medium) rs780740440 Functional Loss SNV dbSNP153 33..33 33 - - - 87936 RMVar_ID_87936 Human_SNP_ID_324247534 m1A Human chr7 + 66537010 66537010 66537010 CTTGCAGGGCCTGGTATTGCGCCTGCCCCTGCAGTGTTCTCAGCAGCTCTCTGAGGCGGTTCTCT CTTGCAGGGCCTGGTATTGCGCCTGCCCCTGCGGTGTTCTCAGCAGCTCTCTGAGGCGGTTCTCT A G AC008267.3 Ensembl:ENSG00000234500 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66536959..66537043 26863196 MeRIP-seq:(Medium) rs571984746 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_494 87937 RMVar_ID_87937 Human_SNP_ID_324249189 m1A Human chr7 + 66541632 66541629 66541632 AGAGGCATTACTCCATGAGATAGGGACACGGGAGGAGGACGTTGTCTGGAATGGCTGATATTTGC AGAGGCATTACTCCATGAGATAGGGACACG___GGAGGACGTTGTCTGGAATGGCTGATATTTGC GGGA G AC008267.3 Ensembl:ENSG00000234500 Pseudogene intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:66541560..66541673 26863196 MeRIP-seq:(Medium) rs10570041 Functional Loss DEL dbSNP153 31..33 33 - - - Clinvar_Rec_495,Clinvar_Rec_496,Clinvar_Rec_497 GWAS_ID_11028,GWAS_ID_11029,GWAS_ID_11030,GWAS_ID_11031,GWAS_ID_11032,GWAS_ID_11033,GWAS_ID_11034,GWAS_ID_11035,GWAS_ID_11036,GWAS_ID_11037,GWAS_ID_11038,GWAS_ID_11039,GWAS_ID_11040,GWAS_ID_11041,GWAS_ID_11042,GWAS_ID_11043,GWAS_ID_11044,GWAS_ID_11045,GWAS_ID_11046,GWAS_ID_11047,GWAS_ID_11048,GWAS_ID_11049,GWAS_ID_11050,GWAS_ID_11051,GWAS_ID_11052,GWAS_ID_11053,GWAS_ID_11054,GWAS_ID_11055,GWAS_ID_11056,GWAS_ID_11057,GWAS_ID_11058,GWAS_ID_11059,GWAS_ID_11060,GWAS_ID_11061,GWAS_ID_11062,GWAS_ID_11063,GWAS_ID_11064,GWAS_ID_11065,GWAS_ID_11066,GWAS_ID_11067,GWAS_ID_11068,GWAS_ID_11069,GWAS_ID_11070,GWAS_ID_11071,GWAS_ID_11072,GWAS_ID_11073,GWAS_ID_11074,GWAS_ID_11075,GWAS_ID_11076,GWAS_ID_11077,GWAS_ID_11078,GWAS_ID_11079,GWAS_ID_11080,GWAS_ID_11081,GWAS_ID_11082,GWAS_ID_11083,GWAS_ID_11084,GWAS_ID_11085,GWAS_ID_11086,GWAS_ID_11087,GWAS_ID_11088,GWAS_ID_11089,GWAS_ID_11090,GWAS_ID_11091,GWAS_ID_11092,GWAS_ID_11093,GWAS_ID_11094,GWAS_ID_11095,GWAS_ID_11096,GWAS_ID_11097,GWAS_ID_11098,GWAS_ID_11099,GWAS_ID_11100,GWAS_ID_11101,GWAS_ID_11102,GWAS_ID_11103,GWAS_ID_11104,GWAS_ID_11105,GWAS_ID_11106,GWAS_ID_11107,GWAS_ID_11108,GWAS_ID_11109,GWAS_ID_11110,GWAS_ID_11111,GWAS_ID_11112,GWAS_ID_11113,GWAS_ID_11114,GWAS_ID_11115,GWAS_ID_11116,GWAS_ID_11117,GWAS_ID_11118,GWAS_ID_11119,GWAS_ID_11120,GWAS_ID_11121,GWAS_ID_11122,GWAS_ID_11123,GWAS_ID_11124,GWAS_ID_11125,GWAS_ID_11126,GWAS_ID_11127,GWAS_ID_11128,GWAS_ID_11129,GWAS_ID_11130,GWAS_ID_11131,GWAS_ID_11132,GWAS_ID_11133,GWAS_ID_11134,GWAS_ID_11135,GWAS_ID_11136,GWAS_ID_11137,GWAS_ID_11138,GWAS_ID_11139,GWAS_ID_11140,GWAS_ID_11141,GWAS_ID_11142,GWAS_ID_11143,GWAS_ID_11144,GWAS_ID_11145,GWAS_ID_11146,GWAS_ID_11147,GWAS_ID_11148 87938 RMVar_ID_87938 Human_SNP_ID_324249192 m1A Human chr7 + 66541632 66541631 66541632 AGAGGCATTACTCCATGAGATAGGGACACGGGAGGAGGACGTTGTCTGGAATGGCTGATATTTGC AGAGGCATTACTCCATGAGATAGGGACACGGG_GGAGGACGTTGTCTGGAATGGCTGATATTTGC GA G AC008267.3 Ensembl:ENSG00000234500 Pseudogene intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:66541560..66541673 26863196 MeRIP-seq:(Medium) rs1554381240 Functional Loss DEL dbSNP153 33..33 33 - - - 87939 RMVar_ID_87939 Human_SNP_ID_324252775 m1A Human chr7 + 66554523 66554523 66554523 CATTCACCTGTCATGGGCCTGAGTGACCTATCACATCCCCAAAACCACCACCTTCCTAGTCCTTC CATTCACCTGTCATGGGCCTGAGTGACCTATCGCATCCCCAAAACCACCACCTTCCTAGTCCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:66554473..66554556 26863196 MeRIP-seq:(Medium) rs1211653317 Functional Loss SNV dbSNP153 33..33 33 - - - 87940 RMVar_ID_87940 Human_SNP_ID_324259271 m1A Human chr7 + 66576819 66576819 66576819 CTTCTGCCTGGCTTTGTGCTACTCTTCCCTCCAGCACTTGGAGCAGAAACCCTGCCAGGTAGGGT CTTCTGCCTGGCTTTGTGCTACTCTTCCCTCCGGCACTTGGAGCAGAAACCCTGCCAGGTAGGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66576817..66576962 26863196 MeRIP-seq:(Medium) rs777155609 Functional Loss SNV dbSNP153 33..33 33 - - - 87941 RMVar_ID_87941 Human_SNP_ID_324260769 m1A Human chr7 - 66582190 66582190 66582190 GAGATTTTTGAACATTTTTAAATAATAGAGACAGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGA GAGATTTTTGAACATTTTTAAATAATAGAGACCGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGA T G AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66582188..66582277 26863196 MeRIP-seq:(Medium) rs557524375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40521,RMVar_hsa_circ_26120,RMVar_hsa_circ_112926,RMVar_hsa_circ_107816,RMVar_hsa_circ_245361,RMVar_hsa_circ_245366,RMVar_hsa_circ_13427 87942 RMVar_ID_87942 Human_SNP_ID_324263803 m1A Human chr7 - 66592292 66592270 66592292 CGGAGTCGAGACCTACCCGAACGACGCGGGCGAGCGGGGCTTTGGACGCCGGTGGAGACGCAGGC CGGAGTCGAGACCTACCCGAACGACGCGGGCG______________________GAGACGCAGGC CCACCGGCGTCCAAAGCCCCGCT C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66592263..66592355 26863410 MeRIP-seq:(Medium) rs998957158 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_8272391,Human_RBP_ID_17431046 Human_Splice_Rec_871351,Human_Splice_Rec_871361,Human_Splice_Rec_871381,Human_Splice_Rec_871391 87943 RMVar_ID_87943 Human_SNP_ID_324274688 m1A Human chr7 + 66629036 66629036 66629036 AGTGCCCGGGGCCGCCGCCTCCGCCCGCCCGAAGCCGCGCCCACTGCCCAGAGCCAGAGGGATGG AGTGCCCGGGGCCGCCGCCTCCGCCCGCCCGAGGCCGCGCCCACTGCCCAGAGCCAGAGGGATGG A G AC027644.4,KCTD7 Ensembl:ENSG00000284461,Ensembl:ENSG00000243335 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:66628935..66629044 26863410 MeRIP-seq:(Medium) rs1277832683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956381 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367 87944 RMVar_ID_87944 Human_SNP_ID_324281815 m1A Human chr7 - 66654599 66654599 66654599 CGTACCTCGCCCGCGGCTTCGCCGACATCCACACAGCCGCTCGCCCGCGTGGCTGCAGTAGGTCT CGTACCTCGCCCGCGGCTTCGCCGACATCCACGCAGCCGCTCGCCCGCGTGGCTGCAGTAGGTCT T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66654548..66654971 26863196 MeRIP-seq:(Medium) rs921498451 Functional Loss SNV dbSNP153 33..33 33 - - - 87945 RMVar_ID_87945 Human_SNP_ID_324281816 m1A Human chr7 - 66654599 66654599 66654599 CGTACCTCGCCCGCGGCTTCGCCGACATCCACACAGCCGCTCGCCCGCGTGGCTGCAGTAGGTCT CGTACCTCGCCCGCGGCTTCGCCGACATCCACCCAGCCGCTCGCCCGCGTGGCTGCAGTAGGTCT T G RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66654548..66654971 26863196 MeRIP-seq:(Medium) rs921498451 Functional Loss SNV dbSNP153 33..33 33 - - - 87946 RMVar_ID_87946 Human_SNP_ID_324282243 m1A Human chr7 - 66655981 66655981 66655981 CCCGATCCCTTCCAGGCTCCACGCCCGACAGCACGGCCTAAATGCCCGACTCCCTCCTCGGTGCT CCCGATCCCTTCCAGGCTCCACGCCCGACAGCGCGGCCTAAATGCCCGACTCCCTCCTCGGTGCT T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66655957..66656144 26863196 MeRIP-seq:(Medium) rs1056452076 Functional Loss SNV dbSNP153 33..33 33 - - - 87947 RMVar_ID_87947 Human_SNP_ID_324285144 m1A Human chr7 - 66666075 66666075 66666075 TGACCATGGAGAACCACATAGGTTTCCCCAGCACACAACCACCTTCCCTCTTCAATAGCTGCTTC TGACCATGGAGAACCACATAGGTTTCCCCAGCGCACAACCACCTTCCCTCTTCAATAGCTGCTTC T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66666071..66666227 26863196 MeRIP-seq:(Medium) rs1358322309 Functional Loss SNV dbSNP153 33..33 33 - - - 87948 RMVar_ID_87948 Human_SNP_ID_324290202 m1A Human chr7 + 66685360 66685360 66685360 TGTCTTGTATTTTAATCTTCTCTGCTCTTTAGATGTTTGAAGTGAGGCCAGGCATGTTGGCTCAC TGTCTTGTATTTTAATCTTCTCTGCTCTTTAGGTGTTTGAAGTGAGGCCAGGCATGTTGGCTCAC A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66685323..66685398 26863196 MeRIP-seq:(Medium) rs1055345356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16196855 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 87949 RMVar_ID_87949 Human_SNP_ID_324290646 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA___________GCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..43 33 - - - 87950 RMVar_ID_87950 Human_SNP_ID_324290647 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA________AAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..40 33 - - - 87951 RMVar_ID_87951 Human_SNP_ID_324290648 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA_______AAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..39 33 - - - 87952 RMVar_ID_87952 Human_SNP_ID_324290649 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA______AAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..38 33 - - - 87953 RMVar_ID_87953 Human_SNP_ID_324290650 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA_____AAAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..37 33 - - - 87954 RMVar_ID_87954 Human_SNP_ID_324290651 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA____AAAAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..36 33 - - - 87955 RMVar_ID_87955 Human_SNP_ID_324290652 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA___AAAAAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..35 33 - - - 87956 RMVar_ID_87956 Human_SNP_ID_324290653 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA__AAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..34 33 - - - 87957 RMVar_ID_87957 Human_SNP_ID_324290654 m1A Human chr7 - 66687124 66687113 66687124 AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT AAGACTCCGTCTCAAAAAAAGAAAAAAAAAAA_AAAAAAAAAAGCCGGGCGTGGTGGCTCGTAAT CTTTTTTTTTTT CTTTTTTTTTT RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:66687113..66687200 26863410 MeRIP-seq:(Medium) rs71526570 Functional Loss DEL dbSNP153 33..33 33 - - - 87958 RMVar_ID_87958 Human_SNP_ID_324292814 m1A Human chr7 + 66695452 66695452 66695452 AGAGAGACCGTCATGGGCAGGGGCTTTGACGCAAGAGGTTCCACAGTGGCTTGGCCCACATGTCA AGAGAGACCGTCATGGGCAGGGGCTTTGACGCCAGAGGTTCCACAGTGGCTTGGCCCACATGTCA A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66695436..66695544 26863196 MeRIP-seq:(Medium) rs1002829189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3866682 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 87959 RMVar_ID_87959 Human_SNP_ID_324292815 m1A Human chr7 + 66695452 66695452 66695452 AGAGAGACCGTCATGGGCAGGGGCTTTGACGCAAGAGGTTCCACAGTGGCTTGGCCCACATGTCA AGAGAGACCGTCATGGGCAGGGGCTTTGACGCGAGAGGTTCCACAGTGGCTTGGCCCACATGTCA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66695436..66695544 26863196 MeRIP-seq:(Medium) rs1002829189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3866682 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 87960 RMVar_ID_87960 Human_SNP_ID_324300705 m1A Human chr7 - 66728706 66728686 66728707 GAGGTGAAGGTGGAGGTGAGGACAGAGCTGAAAGTTGAGGTGAGGATGATGAGGATGGAGGTGAA GAGGTGAAGGTGGAGGTGAGGACAGAGCTGA_____________________GGATGGAGGTGAA CTCATCATCCTCACCTCAACTT C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66728484..66728945 26863196 MeRIP-seq:(Medium) rs1403240252 Functional Loss DEL dbSNP153 32..52 33 - - - 87961 RMVar_ID_87961 Human_SNP_ID_324300717 m1A Human chr7 - 66728706 66728706 66728706 GAGGTGAAGGTGGAGGTGAGGACAGAGCTGAAAGTTGAGGTGAGGATGATGAGGATGGAGGTGAA GAGGTGAAGGTGGAGGTGAGGACAGAGCTGAAGGTTGAGGTGAGGATGATGAGGATGGAGGTGAA T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66728484..66728945 26863196 MeRIP-seq:(Medium) rs1023928270 Functional Loss SNV dbSNP153 33..33 33 - - - 87962 RMVar_ID_87962 Human_SNP_ID_324300729 m1A Human chr7 - 66728731 66728731 66728731 GGCGGTGAGGGTCGAGGTGAGGATGGAGGTGAAGGTGGAGGTGAGGACAGAGCTGAAAGTTGAGG GGCGGTGAGGGTCGAGGTGAGGATGGAGGTGAGGGTGGAGGTGAGGACAGAGCTGAAAGTTGAGG T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:66728716..66728799 26863196 MeRIP-seq:(Medium) rs796438189 Functional Loss SNV dbSNP153 33..33 33 - - - 87963 RMVar_ID_87963 Human_SNP_ID_324304123 m1A Human chr7 - 66740943 66740943 66740943 GGCGGCGCTGACGGAGACGGAATGTGGGACGAAGGACAGCGGGAGGCACCGACGCGCAACTGCCC GGCGGCGCTGACGGAGACGGAATGTGGGACGATGGACAGCGGGAGGCACCGACGCGCAACTGCCC T A RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66740941..66741154 26863196 MeRIP-seq:(Medium) rs1021230538 Functional Loss SNV dbSNP153 33..33 33 - - - 87964 RMVar_ID_87964 Human_SNP_ID_324304124 m1A Human chr7 - 66740943 66740943 66740943 GGCGGCGCTGACGGAGACGGAATGTGGGACGAAGGACAGCGGGAGGCACCGACGCGCAACTGCCC GGCGGCGCTGACGGAGACGGAATGTGGGACGAGGGACAGCGGGAGGCACCGACGCGCAACTGCCC T C RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66740941..66741154 26863196 MeRIP-seq:(Medium) rs1021230538 Functional Loss SNV dbSNP153 33..33 33 - - - 87965 RMVar_ID_87965 Human_SNP_ID_324312157 m1A Human chr7 + 66771837 66771837 66771837 ACTTTTTGTTCATAATTGGTAAGATTTTATTTAGTAGAATGATAATTCATTTTCAACAGCACTTT ACTTTTTGTTCATAATTGGTAAGATTTTATTTGGTAGAATGATAATTCATTTTCAACAGCACTTT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66771835..66772034 26863196 MeRIP-seq:(Medium) rs767951315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16071,RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384,RMVar_hsa_circ_307604,RMVar_hsa_circ_339490,RMVar_hsa_circ_67727,RMVar_hsa_circ_245371,RMVar_hsa_circ_12986 87966 RMVar_ID_87966 Human_SNP_ID_324348607 m1A Human chr7 - 66921112 66921112 66921112 ACAAGCTTCGTCAGAGGCAGGCGGCGGAGACCACGCTTCCGGGACGGGTAGCGTGCATGCGGACG ACAAGCTTCGTCAGAGGCAGGCGGCGGAGACCGCGCTTCCGGGACGGGTAGCGTGCATGCGGACG T C lnc-SBDS-30 RNACentral:URS0000D59F96 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:66920992..66921119 26863196 MeRIP-seq:(Medium) rs1434681682 Functional Loss SNV dbSNP153 33..33 33 - - - 87967 RMVar_ID_87967 Human_SNP_ID_324348706 m1A Human chr7 - 66921348 66921348 66921348 TCGTGGCGGCGCGTGGCGGGCCCGAGGCCGCTAGGCACCATCTTCTCCCCGCGCCGGGGGCAGCG TCGTGGCGGCGCGTGGCGGGCCCGAGGCCGCTCGGCACCATCTTCTCCCCGCGCCGGGGGCAGCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:66921248..66921517 26863196 MeRIP-seq:(Medium) rs2293350 Functional Loss SNV dbSNP153 33..33 33 - - - 87968 RMVar_ID_87968 Human_SNP_ID_324356901 m1A Human chr7 - 66952700 66952700 66952700 TCCCTAAGTCCTTGGATGAAAATGCTGAGATCATCCGTGATTCACTACCCTTTGACCTCCCACAT TCCCTAAGTCCTTGGATGAAAATGCTGAGATCGTCCGTGATTCACTACCCTTTGACCTCCCACAT T C lnc-SBDS-1,lnc-SBDS-1:2 RNACentral:URS00009BE925,RNACentral:URS00009B36E2 lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:66952655..66952981 26863196 MeRIP-seq:(Medium) rs931355224 Functional Loss SNV dbSNP153 33..33 33 - - - 87969 RMVar_ID_87969 Human_SNP_ID_324368467 m1A Human chr7 + 66995352 66995352 66995352 TTGTAGCAGGCGATTTCGAAGCGCTTCCCGGCACGCTTCATCCGTACCACGGCCACATTGGTTAG TTGTAGCAGGCGATTTCGAAGCGCTTCCCGGCGCGCTTCATCCGTACCACGGCCACATTGGTTAG A G TYW1 Ensembl:ENSG00000198874 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66995258..66995366 26863196 MeRIP-seq:(Medium) rs774593246 Functional Loss SNV dbSNP153 33..33 33 - - - 87970 RMVar_ID_87970 Human_SNP_ID_324368521 m1A Human chr7 + 66995452 66995452 66995452 CGGCTGTTCAAAGACCCAGAAGCCGGCGAACCAGGGCTGACCCGCGCCGTCCAGCCTGAAGGCCA CGGCTGTTCAAAGACCCAGAAGCCGGCGAACCCGGGCTGACCCGCGCCGTCCAGCCTGAAGGCCA A C TYW1 Ensembl:ENSG00000198874 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:66995401..66995552 32194978 MeRIP-seq:(Medium) rs772607723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_871775 87971 RMVar_ID_87971 Human_SNP_ID_324368533 m1A Human chr7 + 66995478 66995478 66995478 CGAACCAGGGCTGACCCGCGCCGTCCAGCCTGAAGGCCACCAGCGCCTCGCGGTAACGACCGATC CGAACCAGGGCTGACCCGCGCCGTCCAGCCTGTAGGCCACCAGCGCCTCGCGGTAACGACCGATC A T TYW1 Ensembl:ENSG00000198874 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:66995376..66995575 26863410 MeRIP-seq:(Medium) rs1448884859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_871775 87972 RMVar_ID_87972 Human_SNP_ID_324368550 m1A Human chr7 + 66995536 66995536 66995536 ACCGATCGGCGCGCGGCACTGACCCAACCACCAGTGCGCGGCGCCGCGACTCACTAGCTTCAGGC ACCGATCGGCGCGCGGCACTGACCCAACCACCTGTGCGCGGCGCCGCGACTCACTAGCTTCAGGC A T TYW1 Ensembl:ENSG00000198874 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66995401..66995600 26863196 MeRIP-seq:(Medium) rs879198009 Functional Loss SNV dbSNP153 33..33 33 - - - 87973 RMVar_ID_87973 Human_SNP_ID_324368551 m1A Human chr7 - 66995538 66995538 66995538 CTGCCTGAAGCTAGTGAGTCGCGGCGCCGCGCACTGGTGGTTGGGTCAGTGCCGCGCGCCGATCG CTGCCTGAAGCTAGTGAGTCGCGGCGCCGCGCGCTGGTGGTTGGGTCAGTGCCGCGCGCCGATCG T C SBDS Ensembl:ENSG00000126524 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:66995426..66995600 26863196 MeRIP-seq:(Medium) rs1410718042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173457,Human_RBP_ID_4956392,Human_RBP_ID_5327866,Human_RBP_ID_5513583,Human_RBP_ID_18103135 RMVar_hsa_circ_91735,RMVar_hsa_circ_81458,RMVar_hsa_circ_245409,RMVar_hsa_circ_245413 87974 RMVar_ID_87974 Human_SNP_ID_324376285 m1A Human chr7 - 67024852 67024844 67024852 TTCAGAAATACATTGTTCAAAGGGGCAAAGGCAAAGCTCTCTTACCCTCCCTCCCACACTGAGAA TTCAGAAATACATTGTTCAAAGGGGCAAAGGC________CTTACCCTCCCTCCCACACTGAGAA GAGAGCTTT G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:67024849..67024914 26863196 MeRIP-seq:(Medium) rs766972724 Functional Loss DEL dbSNP153 33..40 33 - - - 87975 RMVar_ID_87975 Human_SNP_ID_324376288 m1A Human chr7 - 67024852 67024848 67024852 TTCAGAAATACATTGTTCAAAGGGGCAAAGGCAAAGCTCTCTTACCCTCCCTCCCACACTGAGAA TTCAGAAATACATTGTTCAAAGGGGCAAAGGC____CTCTCTTACCCTCCCTCCCACACTGAGAA GCTTT G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:67024849..67024914 26863196 MeRIP-seq:(Medium) rs1562971085 Functional Loss DEL dbSNP153 33..36 33 - - - 87976 RMVar_ID_87976 Human_SNP_ID_324376351 m1A Human chr7 - 67025024 67025024 67025024 GAGCCAAGTGCAACATTTCCCAAAGTAACGGTACCTTTTCTTTCTTCACATGATCCATAATTTTG GAGCCAAGTGCAACATTTCCCAAAGTAACGGTGCCTTTTCTTTCTTCACATGATCCATAATTTTG T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:67024980..67025064 26863196 MeRIP-seq:(Medium) rs1332613958 Functional Loss SNV dbSNP153 33..33 33 - - - 87977 RMVar_ID_87977 Human_SNP_ID_324444731 m1A Human chr7 + 67309619 67309619 67309619 GTAAGAGTTGCCCTCCAACTGAGTCTGCACGAAGATATCAATCAGCGTCAGTATGAGGCTGAAAG GTAAGAGTTGCCCTCCAACTGAGTCTGCACGAGGATATCAATCAGCGTCAGTATGAGGCTGAAAG A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:67308998..67309619 32194978 MeRIP-seq:(Medium) rs768233837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955422,Human_RBP_ID_3867462,Human_RBP_ID_5104700,Human_RBP_ID_5623482,Human_RBP_ID_8272131 Human_Splice_Rec_871934,Human_Splice_Rec_871935,Human_Splice_Rec_871942,Human_Splice_Rec_871950,Human_Splice_Rec_871951,Human_Splice_Rec_871966 RMVar_hsa_circ_114448,RMVar_hsa_circ_82376,RMVar_hsa_circ_245446,RMVar_hsa_circ_245447,RMVar_hsa_circ_333990,RMVar_hsa_circ_245448 87978 RMVar_ID_87978 Human_SNP_ID_325329589 m1A Human chr7 + 70764883 70764883 70764883 CAGCCCCCTGCACAGCTTCACACCCACCCTCCAGCCCCCCGCACACTCACATCACCCCAATATGT CAGCCCCCTGCACAGCTTCACACCCACCCTCCCGCCCCCCGCACACTCACATCACCCCAATATGT A C AUTS2 Ensembl:ENSG00000158321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:70763064..70764973 26863196 MeRIP-seq:(Medium) rs1422934990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1114671,Human_RBP_ID_17313608,Human_RBP_ID_22424569 RMVar_hsa_circ_119594,RMVar_hsa_circ_245462,RMVar_hsa_circ_75596,RMVar_hsa_circ_245461,RMVar_hsa_circ_116770,RMVar_hsa_circ_288007,RMVar_hsa_circ_302584,RMVar_hsa_circ_316911,RMVar_hsa_circ_49339,RMVar_hsa_circ_67677,RMVar_hsa_circ_245493,RMVar_hsa_circ_245494,RMVar_hsa_circ_245492,RMVar_hsa_circ_245495 87979 RMVar_ID_87979 Human_SNP_ID_325329590 m1A Human chr7 + 70764883 70764883 70764883 CAGCCCCCTGCACAGCTTCACACCCACCCTCCAGCCCCCCGCACACTCACATCACCCCAATATGT CAGCCCCCTGCACAGCTTCACACCCACCCTCCGGCCCCCCGCACACTCACATCACCCCAATATGT A G AUTS2 Ensembl:ENSG00000158321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:70763064..70764973 26863196 MeRIP-seq:(Medium) rs1422934990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1114671,Human_RBP_ID_17313608,Human_RBP_ID_22424569 RMVar_hsa_circ_119594,RMVar_hsa_circ_245462,RMVar_hsa_circ_75596,RMVar_hsa_circ_245461,RMVar_hsa_circ_116770,RMVar_hsa_circ_288007,RMVar_hsa_circ_302584,RMVar_hsa_circ_316911,RMVar_hsa_circ_49339,RMVar_hsa_circ_67677,RMVar_hsa_circ_245493,RMVar_hsa_circ_245494,RMVar_hsa_circ_245492,RMVar_hsa_circ_245495 87980 RMVar_ID_87980 Human_SNP_ID_325330034 m1A Human chr7 - 70766309 70766309 70766309 TACGCACCATGGGAGGTGCTGGCGTCGGCATGATGGCGGTGGGTGGGATGGCGTGGGGGAACGGC TACGCACCATGGGAGGTGCTGGCGTCGGCATGGTGGCGGTGGGTGGGATGGCGTGGGGGAACGGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:70766209..70766331 26863196 MeRIP-seq:(Medium) rs772644555 Functional Loss SNV dbSNP153 33..33 33 - - - 87981 RMVar_ID_87981 Human_SNP_ID_325336820 m1A Human chr7 + 70790834 70790834 70790834 CGCATCAGCCCCACCGCGGGCAACCAGAACGGACTCCTCAACAAGACCCCTCCGACAGCAGCGCT CGCATCAGCCCCACCGCGGGCAACCAGAACGGCCTCCTCAACAAGACCCCTCCGACAGCAGCGCT A C AUTS2 Ensembl:ENSG00000158321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:70790724..70790875 26863196 MeRIP-seq:(Medium) rs1554489422 Functional Loss SNV dbSNP153 33..33 33 - - - 87982 RMVar_ID_87982 Human_SNP_ID_325888164 m1A Human chr7 + 72829550 72829550 72829550 GAGTCGCGGCGCCGCGCACTTGTGGTTGGGTCAGTGCCGCGCGCCGCTCGGTCGTTACCGCGAGG GAGTCGCGGCGCCGCGCACTTGTGGTTGGGTCGGTGCCGCGCGCCGCTCGGTCGTTACCGCGAGG A G SBDSP1 Ensembl:ENSG00000225648 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:72829501..72829675 26863196 MeRIP-seq:(Medium) rs1427909873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4947842,Human_RBP_ID_7779070,Human_RBP_ID_9216407,Human_RBP_ID_10485617,Human_RBP_ID_17171248,Human_RBP_ID_17674090,Human_RBP_ID_21960692,Human_RBP_ID_22372465,Human_RBP_ID_24225183 87983 RMVar_ID_87983 Human_SNP_ID_325901458 m1A Human chr7 + 72879588 72879588 72879588 CCGGAGCCAGCGGCGCTGGGGCCAGAGGGGCCAGGCGGGAGGTGGTGGCGGAGGCGAAGGGGCGA CCGGAGCCAGCGGCGCTGGGGCCAGAGGGGCCGGGCGGGAGGTGGTGGCGGAGGCGAAGGGGCGA A G POM121 Ensembl:ENSG00000196313 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:72879401..72879650 26863196 MeRIP-seq:(Medium) rs2072300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794024,Human_RBP_ID_4955808,Human_RBP_ID_5327867 GWAS_ID_11149,GWAS_ID_11150,GWAS_ID_11151 RMVar_hsa_circ_110500,RMVar_hsa_circ_245527 87984 RMVar_ID_87984 Human_SNP_ID_325901519 m1A Human chr7 + 72879798 72879797 72879798 CAGAACAGCCTTGGTGAGGTGGACGGGAGGGGACTTCGCGAGCAGACGCGCGCGCCAGCGACAGC CAGAACAGCCTTGGTGAGGTGGACGGGAGGGG_CTTCGCGAGCAGACGCGCGCGCCAGCGACAGC GA G POM121 Ensembl:ENSG00000196313 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:72879742..72879840 26863196 MeRIP-seq:(Medium) rs1191159796 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_86169,Human_RBP_ID_843794,Human_RBP_ID_4947887,Human_RBP_ID_5429719,Human_RBP_ID_5513633,Human_RBP_ID_16209590,Human_RBP_ID_22112328,Human_RBP_ID_26356503 Human_Splice_Rec_872695 RMVar_hsa_circ_110500,RMVar_hsa_circ_245527 87985 RMVar_ID_87985 Human_SNP_ID_325903911 m1A Human chr7 - 72890678 72890678 72890678 GTATGTTATCTTCTCATCAGGGTCCAGTTGCCACCACTCCTCCTGGGTGAAATCCACAGCCACAT GTATGTTATCTTCTCATCAGGGTCCAGTTGCCGCCACTCCTCCTGGGTGAAATCCACAGCCACAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:72890597..72890679;chr7:72890596..72890679 26863196 MeRIP-seq:(Medium) rs1463610393 Functional Loss SNV dbSNP153 33..33 33 - - - 87986 RMVar_ID_87986 Human_SNP_ID_325910069 m1A Human chr7 + 72917745 72917744 72917746 CCCTGTGTGCAGCGATGAGAGAGTGTAGAAAGAAAGACACAAGACAAAGAGATAAAAGAAAAGAC CCCTGTGTGCAGCGATGAGAGAGTGTAGAAAG__AGACACAAGACAAAGAGATAAAAGAAAAGAC GAA G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:72917700..72917787 26863196 MeRIP-seq:(Medium) rs1554495323 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16210200 RMVar_hsa_circ_312976 87987 RMVar_ID_87987 Human_SNP_ID_325912151 m1A Human chr7 + 72925548 72925548 72925548 CGGAACTGCTACTCATGGGCAGTTACCTGGGCAAGCCCGGGCCGCCGCAGCCCGCCGCCGCTCCG CGGAACTGCTACTCATGGGCAGTTACCTGGGCGAGCCCGGGCCGCCGCAGCCCGCCGCCGCTCCG A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:72925533..72925637 26863196 MeRIP-seq:(Medium) rs1457227348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26794506 RMVar_hsa_circ_312976 87988 RMVar_ID_87988 Human_SNP_ID_325912162 m1A Human chr7 + 72925564 72925564 72925564 GGGCAGTTACCTGGGCAAGCCCGGGCCGCCGCAGCCCGCCGCCGCTCCGGAGGGCCAGGACCTGC GGGCAGTTACCTGGGCAAGCCCGGGCCGCCGCGGCCCGCCGCCGCTCCGGAGGGCCAGGACCTGC A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:72925533..72925644 26863196 MeRIP-seq:(Medium) rs782333597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26794506 RMVar_hsa_circ_312976 87989 RMVar_ID_87989 Human_SNP_ID_325912192 m1A Human chr7 - 72925622 72925622 72925622 CGCGGCGGTGGGGAGCGCGGCGCCGGGCGGGCAGGTGGGCGGCGGCCAGGCCTATCCCGCAGGTC CGCGGCGGTGGGGAGCGCGGCGCCGGGCGGGCGGGTGGGCGGCGGCCAGGCCTATCCCGCAGGTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:72925526..72925750 26863410 MeRIP-seq:(Medium) rs1295052582 Functional Loss SNV dbSNP153 33..33 33 - - - 87990 RMVar_ID_87990 Human_SNP_ID_325912198 m1A Human chr7 + 72925661 72925632 72925662 CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CCGG______________________________CGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC GCGCCGCGCTCCCCACCGCCGCGCTCCCCAC G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:72925577..72925678 26863410 MeRIP-seq:(Medium) rs531690539 Functional Loss DEL dbSNP153 5..34 33 - - - RMVar_hsa_circ_312976 87991 RMVar_ID_87991 Human_SNP_ID_325912199 m1A Human chr7 + 72925661 72925632 72925662 CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CCGGCGCCGCGCTCCCCAC_______________CGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC GCGCCGCGCTCCCCACCGCCGCGCTCCCCAC GCGCCGCGCTCCCCAC POM121 Ensembl:ENSG00000196313 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:72925577..72925678 26863410 MeRIP-seq:(Medium) rs531690539 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_312976 87992 RMVar_ID_87992 Human_SNP_ID_325912221 m1A Human chr7 + 72925661 72925660 72925661 CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCC_CCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CA C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:72925577..72925678 26863410 MeRIP-seq:(Medium) rs1554497136 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_312976 87993 RMVar_ID_87993 Human_SNP_ID_325912222 m1A Human chr7 + 72925661 72925661 72925661 CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC A C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:72925577..72925678 26863410 MeRIP-seq:(Medium) rs1389469051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312976 87994 RMVar_ID_87994 Human_SNP_ID_325912266 m1A Human chr7 + 72925696 72925696 72925696 GCCGCGCTCCCCCCCGCCCTCCCCGCCGACCCATCGCGCTCACCACGTTTACCCCTCTCTGCCCA GCCGCGCTCCCCCCCGCCCTCCCCGCCGACCCCTCGCGCTCACCACGTTTACCCCTCTCTGCCCA A C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:72925583..72925715 26863196 MeRIP-seq:(Medium) rs1554497189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_872801 RMVar_hsa_circ_312976 87995 RMVar_ID_87995 Human_SNP_ID_325912267 m1A Human chr7 + 72925696 72925696 72925696 GCCGCGCTCCCCCCCGCCCTCCCCGCCGACCCATCGCGCTCACCACGTTTACCCCTCTCTGCCCA GCCGCGCTCCCCCCCGCCCTCCCCGCCGACCCGTCGCGCTCACCACGTTTACCCCTCTCTGCCCA A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:72925583..72925715 26863196 MeRIP-seq:(Medium) rs1554497189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_872801 RMVar_hsa_circ_312976 87996 RMVar_ID_87996 Human_SNP_ID_325917607 m1A Human chr7 + 72944818 72944818 72944818 AGGGGTCGGGGAGAGGAGGTCATGGGGGTGGCAGGGTTGAGGGGCTGAGAGGACCATCAGTCAGC AGGGGTCGGGGAGAGGAGGTCATGGGGGTGGCCGGGTTGAGGGGCTGAGAGGACCATCAGTCAGC A C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:72944805..72944895 26863196 MeRIP-seq:(Medium) rs1339180626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14411,Human_RBP_ID_843796,Human_RBP_ID_7756387,Human_RBP_ID_9439273,Human_RBP_ID_18959287,Human_RBP_ID_22110827,Human_RBP_ID_22730257 87997 RMVar_ID_87997 Human_SNP_ID_325920426 m1A Human chr7 + 72954595 72954595 72954595 CGTCCCACCCCACCCCGGGTTCCTCACCCCCCACCCCTACTTGTGGCGCGCGGGCCCGCTACCTG CGTCCCACCCCACCCCGGGTTCCTCACCCCCCCCCCCTACTTGTGGCGCGCGGGCCCGCTACCTG A C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:72954573..72954653 26863196 MeRIP-seq:(Medium) rs1339757737 Functional Loss SNV dbSNP153 33..33 33 - - - 87998 RMVar_ID_87998 Human_SNP_ID_325923234 m1A Human chr7 - 72969170 72969169 72969170 GCACAGTGGGAGCGCGTGGGGCATGATGGGACACATGGCGAGGCCGTCAGGGCACAGGGGAAGCA GCACAGTGGGAGCGCGTGGGGCATGATGGGAC_CATGGCGAGGCCGTCAGGGCACAGGGGAAGCA GT G TRIM74 Ensembl:ENSG00000155428 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:72969140..72969243 26863196 MeRIP-seq:(Medium) rs1397214543 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3864154,Human_RBP_ID_5152949,Human_RBP_ID_5327868,Human_RBP_ID_8730724,Human_RBP_ID_21951169,Human_RBP_ID_21992418,Human_RBP_ID_22482994,Human_RBP_ID_26793950 87999 RMVar_ID_87999 Human_SNP_ID_325928907 m1A Human chr7 - 72995807 72995807 72995807 TCTCCTCCAGGTAGCTGGGGTTACAGGTGTGCAGCACCACACCTGGCTAATTTTTTTATTTTTAG TCTCCTCCAGGTAGCTGGGGTTACAGGTGTGCTGCACCACACCTGGCTAATTTTTTTATTTTTAG T A STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1341534041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17430492,Human_RBP_ID_18409748 88000 RMVar_ID_88000 Human_SNP_ID_325928908 m1A Human chr7 - 72995807 72995807 72995807 TCTCCTCCAGGTAGCTGGGGTTACAGGTGTGCAGCACCACACCTGGCTAATTTTTTTATTTTTAG TCTCCTCCAGGTAGCTGGGGTTACAGGTGTGCCGCACCACACCTGGCTAATTTTTTTATTTTTAG T G STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1341534041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17430492,Human_RBP_ID_18409748 88001 RMVar_ID_88001 Human_SNP_ID_325931300 m1A Human chr7 + 73005823 73005823 73005823 AGACACCAACGCTCGGAAACCGCCAGACACCAACGCTCGGAAACCGCCAGACACCAAGGCTCGGA AGACACCAACGCTCGGAAACCGCCAGACACCAGCGCTCGGAAACCGCCAGACACCAAGGCTCGGA A G PMS2P7 Ensembl:ENSG00000229018 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:73005730..73005887 26863410 MeRIP-seq:(Medium) rs1237364631 Functional Loss SNV dbSNP153 33..33 33 - - - 88002 RMVar_ID_88002 Human_SNP_ID_325945672 m1A Human chr7 - 73155014 73155014 73155014 GGGAGCCGCGGGGCGAGGGAGGCAGCGCCGGCAGAGCAGCAGCCGAGGGGCCGAGCGGCGGAGCA GGGAGCCGCGGGGCGAGGGAGGCAGCGCCGGCGGAGCAGCAGCCGAGGGGCCGAGCGGCGGAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr7:73154966..73155059;chr7:73154934..73155110;chr7:73154965..73155047 26863196 MeRIP-seq:(Medium) rs231660 Functional Loss SNV dbSNP153 33..33 33 - - - 88003 RMVar_ID_88003 Human_SNP_ID_325975418 m1A Human chr7 + 73304329 73304329 73304329 GACCGCCAGGAAGTCCTCCTCAGCCAGTTCACAGCAAGAGACGCCAGCCCGGGCCAGCAGCGTGG GACCGCCAGGAAGTCCTCCTCAGCCAGTTCACGGCAAGAGACGCCAGCCCGGGCCAGCAGCGTGG A G RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:73304278..73304378 32194978 MeRIP-seq:(Medium) rs782647057 Functional Loss SNV dbSNP153 33..33 33 - - - 88004 RMVar_ID_88004 Human_SNP_ID_325976367 m1A Human chr7 + 73307669 73307669 73307669 GATGAACCTTGAGCCGAGCCAACTCAGCCTTGAGCCTCGCCTGGTGCCGGCCCAACAGAGCCTTC GATGAACCTTGAGCCGAGCCAACTCAGCCTTGGGCCTCGCCTGGTGCCGGCCCAACAGAGCCTTC A G RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:73307619..73307804 26863196 MeRIP-seq:(Medium) rs781847706 Functional Loss SNV dbSNP153 33..33 33 - - - 88005 RMVar_ID_88005 Human_SNP_ID_325976557 m1A Human chr7 - 73308378 73308378 73308378 GGGAAGTGAACCCCGACGGTCAGCGCTTTGTCATCTGGTCTCAGCTCTGCTGCCGTGCACGGCGG GGGAAGTGAACCCCGACGGTCAGCGCTTTGTCGTCTGGTCTCAGCTCTGCTGCCGTGCACGGCGG T C NSUN5 Ensembl:ENSG00000130305 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:73308376..73308768 32194978 MeRIP-seq:(Medium) rs1201226171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5402158,Human_RBP_ID_19134952 88006 RMVar_ID_88006 Human_SNP_ID_325976754 m1A Human chr7 + 73308750 73308750 73308750 CCAACCCCTTGATAGAGCCCTGGCGGCTCTCCACGCCGGCCAACACGCCTGCAGCTGCAGCATAC CCAACCCCTTGATAGAGCCCTGGCGGCTCTCCGCGCCGGCCAACACGCCTGCAGCTGCAGCATAC A G RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:73308671..73308825;chr7:73308656..73308800 26863196 MeRIP-seq:(Medium) rs782610569 Functional Loss SNV dbSNP153 33..33 33 - - - 88007 RMVar_ID_88007 Human_SNP_ID_325976765 m1A Human chr7 + 73308770 73308770 73308770 TGGCGGCTCTCCACGCCGGCCAACACGCCTGCAGCTGCAGCATACAGCCCCATGTTCCCGCGCGC TGGCGGCTCTCCACGCCGGCCAACACGCCTGCCGCTGCAGCATACAGCCCCATGTTCCCGCGCGC A C RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73308671..73308800 26863196 MeRIP-seq:(Medium) rs1554542413 Functional Loss SNV dbSNP153 33..33 33 - - - 88008 RMVar_ID_88008 Human_SNP_ID_325976766 m1A Human chr7 + 73308770 73308770 73308770 TGGCGGCTCTCCACGCCGGCCAACACGCCTGCAGCTGCAGCATACAGCCCCATGTTCCCGCGCGC TGGCGGCTCTCCACGCCGGCCAACACGCCTGCTGCTGCAGCATACAGCCCCATGTTCCCGCGCGC A T RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73308671..73308800 26863196 MeRIP-seq:(Medium) rs1554542413 Functional Loss SNV dbSNP153 33..33 33 - - - 88009 RMVar_ID_88009 Human_SNP_ID_326009517 m1A Human chr7 - 73433864 73433864 73433864 CGCCCACGTGTGTCCGGGCGCCCTGGGCAGCGAGCGGGCAGCCGCCCGAGGGACAGGAGCCGCCG CGCCCACGTGTGTCCGGGCGCCCTGGGCAGCGGGCGGGCAGCCGCCCGAGGGACAGGAGCCGCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:73433815..73433909 26863196 MeRIP-seq:(Medium) rs1218458703 Functional Loss SNV dbSNP153 33..33 33 - - - 88010 RMVar_ID_88010 Human_SNP_ID_326021462 m1A Human chr7 - 73477093 73477093 73477093 AACGGCTTGCTGTGTTGAAGGAAGAAAATGATAAGAAGAGAGCAGAGAAACAGAAACGGAAAGAA AACGGCTTGCTGTGTTGAAGGAAGAAAATGATCAGAAGAGAGCAGAGAAACAGAAACGGAAAGAA T G BAZ1B Ensembl:ENSG00000009954 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73476920..73477175 26863196 MeRIP-seq:(Medium) rs782392160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792737,Human_RBP_ID_2046619,Human_RBP_ID_4948208,Human_RBP_ID_24225471,Human_RBP_ID_24549116 RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,RMVar_hsa_circ_51151,RMVar_hsa_circ_245564,RMVar_hsa_circ_36970,RMVar_hsa_circ_127994,RMVar_hsa_circ_359696,RMVar_hsa_circ_113364,RMVar_hsa_circ_107344,RMVar_hsa_circ_245567,RMVar_hsa_circ_245569,RMVar_hsa_circ_245568,RMVar_hsa_circ_286407,RMVar_hsa_circ_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_245576,RMVar_hsa_circ_275942,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_281643,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490,RMVar_hsa_circ_245578 88011 RMVar_ID_88011 Human_SNP_ID_326021690 m1A Human chr7 + 73478042 73478042 73478042 TCTTTGTAGTATGCAATGAGGTGTAGGGCTGCAGGAGGCAGATGTTTATGAGGTTTACTAGAGGT TCTTTGTAGTATGCAATGAGGTGTAGGGCTGCGGGAGGCAGATGTTTATGAGGTTTACTAGAGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73477996..73478067 26863196 MeRIP-seq:(Medium) rs1554573135 Functional Loss SNV dbSNP153 33..33 33 - - - 88012 RMVar_ID_88012 Human_SNP_ID_326034024 m1A Human chr7 + 73521906 73521906 73521906 CTCCTCTCCGGGCAACGGCTTCACCAGCGGGAAGGGCTTGCGGCCCAGGAGCGGCGCCATCGCGG CTCCTCTCCGGGCAACGGCTTCACCAGCGGGACGGGCTTGCGGCCCAGGAGCGGCGCCATCGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73521826..73522269 26863196 MeRIP-seq:(Medium) rs994850356 Functional Loss SNV dbSNP153 33..33 33 - - - 88013 RMVar_ID_88013 Human_SNP_ID_326034048 m1A Human chr7 - 73521955 73521955 73521955 GCTGCGCCGCGGGGCCGGCCCCAGCAGCCGCCAGTCCCCACCGCCGCCGCCGCGATGGCGCCGCT GCTGCGCCGCGGGGCCGGCCCCAGCAGCCGCCGGTCCCCACCGCCGCCGCCGCGATGGCGCCGCT T C BAZ1B Ensembl:ENSG00000009954 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:73521873..73522000 26863410 MeRIP-seq:(Medium) rs1349849239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4948311,Human_RBP_ID_8914424,Human_RBP_ID_9311308,Human_RBP_ID_9403446,Human_RBP_ID_22534317 Human_miRNA_ID_2725340,Human_miRNA_ID_2725341 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 88014 RMVar_ID_88014 Human_SNP_ID_326038408 m1A Human chr7 - 73536701 73536701 73536701 GGTCCTACCTCTCACGGGCACCCTAGCTGCTGACAGCCCTTTGTGGCCGCCGTCCCCATCCCCTG GGTCCTACCTCTCACGGGCACCCTAGCTGCTGGCAGCCCTTTGTGGCCGCCGTCCCCATCCCCTG T C BCL7B Ensembl:ENSG00000106635 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:73536651..73536855 32194978 MeRIP-seq:(Medium) rs1179090053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17426959,Human_RBP_ID_26550575 88015 RMVar_ID_88015 Human_SNP_ID_326038516 m1A Human chr7 + 73537103 73537103 73537103 GCAAAAAAGACATGAGCGCTCCTCTTCTCGGGAGCAAGTAGACACAGGTGCCAGGGTCAGGAAGA GCAAAAAAGACATGAGCGCTCCTCTTCTCGGGTGCAAGTAGACACAGGTGCCAGGGTCAGGAAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73537052..73537391 26863196 MeRIP-seq:(Medium) rs756856634 Functional Loss SNV dbSNP153 33..33 33 - - - 88016 RMVar_ID_88016 Human_SNP_ID_326040327 m1A Human chr7 - 73543642 73543642 73543642 TGTCATATTCCTCTTTTTTTCCTTTTCTAGAAAGAAAAGTCAAAATCGAACAGTTCAGCAGCCCG TGTCATATTCCTCTTTTTTTCCTTTTCTAGAAGGAAAAGTCAAAATCGAACAGTTCAGCAGCCCG T C BCL7B Ensembl:ENSG00000106635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:73543526..73543712;chr7:73543570..73543715 26863196 MeRIP-seq:(Medium) rs782178370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_873646,Human_Splice_Rec_873647,Human_Splice_Rec_873656,Human_Splice_Rec_873657,Human_Splice_Rec_873664,Human_Splice_Rec_873665,Human_Splice_Rec_873682,Human_Splice_Rec_873683,Human_Splice_Rec_873702,Human_Splice_Rec_873703,Human_Splice_Rec_873709,Human_Splice_Rec_873730,Human_Splice_Rec_873731,Human_Splice_Rec_873733 RMVar_hsa_circ_245586,RMVar_hsa_circ_290418 88017 RMVar_ID_88017 Human_SNP_ID_326042856 m1A Human chr7 + 73553643 73553643 73553643 TGCAGTGAGCCGAGATTGCGCCAATGCACTCCAGCCTGGGTGACAGAGCGAGATTCCGTCTCAAA TGCAGTGAGCCGAGATTGCGCCAATGCACTCCGGCCTGGGTGACAGAGCGAGATTCCGTCTCAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73553640..73553711 26863196 MeRIP-seq:(Medium) rs530422652 Functional Loss SNV dbSNP153 33..33 33 - - - 88018 RMVar_ID_88018 Human_SNP_ID_326049691 m1A Human chr7 - 73578522 73578522 73578522 CCAACATGGAGCTCTCGCAGATGTCGGAGCTCATGGGGCTGTCGGTGTTGCTTGGGCTGCTGGCC CCAACATGGAGCTCTCGCAGATGTCGGAGCTCTTGGGGCTGTCGGTGTTGCTTGGGCTGCTGGCC T A TBL2 Ensembl:ENSG00000106638 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73578367..73578575 26863196 MeRIP-seq:(Medium) rs1300300981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4948450,Human_RBP_ID_18426026,Human_RBP_ID_22463540,Human_RBP_ID_23080321,Human_RBP_ID_24225573 Human_miRNA_ID_2893880,Human_miRNA_ID_2893881 88019 RMVar_ID_88019 Human_SNP_ID_326055478 m1A Human chr7 - 73597643 73597643 73597643 CTTCCTGAGTTCTGATTTCCTCCTTCCTGAAGACCCCAAGCCCCGGCTCCCACCCCCTCCTGTAC CTTCCTGAGTTCTGATTTCCTCCTTCCTGAAGGCCCCAAGCCCCGGCTCCCACCCCCTCCTGTAC T C MLXIPL Ensembl:ENSG00000009950 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:73597594..73597754 26863196 MeRIP-seq:(Medium) rs537011212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134542,Human_RBP_ID_9403460,Human_RBP_ID_17092303,Human_RBP_ID_18959291 Human_Splice_Rec_873932,Human_Splice_Rec_873962,Human_Splice_Rec_873994,Human_Splice_Rec_874026,Human_Splice_Rec_874056,Human_Splice_Rec_874086,Human_Splice_Rec_874114,Human_Splice_Rec_874122 88020 RMVar_ID_88020 Human_SNP_ID_326055496 m1A Human chr7 - 73597706 73597706 73597706 AGTGTCTGTCTGTCCCCCCAACCAGGCTCGGAACAGCTGCCCTGGCCCCTTGGACTCCAGCGCCT AGTGTCTGTCTGTCCCCCCAACCAGGCTCGGAGCAGCTGCCCTGGCCCCTTGGACTCCAGCGCCT T C MLXIPL Ensembl:ENSG00000009950 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73597472..73597744 26863196 MeRIP-seq:(Medium) rs782379940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134842,Human_RBP_ID_19020917,Human_RBP_ID_23080552,Human_RBP_ID_23120493 Human_Splice_Rec_873932,Human_Splice_Rec_873962,Human_Splice_Rec_873994,Human_Splice_Rec_874026,Human_Splice_Rec_874056,Human_Splice_Rec_874086,Human_Splice_Rec_874114,Human_Splice_Rec_874122 88021 RMVar_ID_88021 Human_SNP_ID_326056689 m1A Human chr7 + 73601970 73601970 73601970 CCCTCTGGGTGTCTGTCGCTCCGTCTGAGGCCATGTGAACCTGTCCTGCCATGATAGCATGGTGC CCCTCTGGGTGTCTGTCGCTCCGTCTGAGGCCCTGTGAACCTGTCCTGCCATGATAGCATGGTGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73601966..73602139 26863196 MeRIP-seq:(Medium) rs765442528 Functional Loss SNV dbSNP153 33..33 33 - - - 88022 RMVar_ID_88022 Human_SNP_ID_326075672 m1A Human chr7 + 73671670 73671670 73671670 TGATGGACCAGCCCCGTTAAAGAACTTGACTCAACTACAGGGGCCTGGGAAGATGCCTGGGTCCC TGATGGACCAGCCCCGTTAAAGAACTTGACTCGACTACAGGGGCCTGGGAAGATGCCTGGGTCCC A G VPS37D Ensembl:ENSG00000176428 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:73671619..73671718 32194978 MeRIP-seq:(Medium) rs1379151061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17713440,Human_RBP_ID_18103844 RMVar_hsa_circ_78313,RMVar_hsa_circ_245590 88023 RMVar_ID_88023 Human_SNP_ID_326078696 m1A Human chr7 + 73682989 73682989 73682989 CCGGGGGAGGCCCGAGAACCGTCGTGGGTCCGAGAGGTGGGCGGCGGGGTACGCGGCGAGCCGGG CCGGGGGAGGCCCGAGAACCGTCGTGGGTCCGGGAGGTGGGCGGCGGGGTACGCGGCGAGCCGGG A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:73682944..73683076 26863196 MeRIP-seq:(Medium) rs782457973 Functional Loss SNV dbSNP153 33..33 33 - - - 88024 RMVar_ID_88024 Human_SNP_ID_326078705 m1A Human chr7 - 73683006 73683006 73683006 GGACGCCCGCACCCGACCCCGGCTCGCCGCGTACCCCGCCGCCCACCTCTCGGACCCACGACGGT GGACGCCCGCACCCGACCCCGGCTCGCCGCGTCCCCCGCCGCCCACCTCTCGGACCCACGACGGT T G DNAJC30 Ensembl:ENSG00000176410 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:73682955..73683056;chr7:73682956..73683114 26863196 MeRIP-seq:(Medium) rs782206269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27533500 88025 RMVar_ID_88025 Human_SNP_ID_326078714 m1A Human chr7 - 73683023 73683023 73683023 TGGCGTCCGGCCCTCCAGGACGCCCGCACCCGACCCCGGCTCGCCGCGTACCCCGCCGCCCACCT TGGCGTCCGGCCCTCCAGGACGCCCGCACCCGCCCCCGGCTCGCCGCGTACCCCGCCGCCCACCT T G DNAJC30 Ensembl:ENSG00000176410 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:73682901..73683155 26863410 MeRIP-seq:(Medium) rs782033892 Functional Loss SNV dbSNP153 33..33 33 - - - 88026 RMVar_ID_88026 Human_SNP_ID_326080094 m1A Human chr7 - 73686686 73686686 73686686 GGTAACAGGGCTTATTCTCTGGCAGATAAAGAAGCTCCAATGCTCGCCCAGCCATCCTGGTCTGG GGTAACAGGGCTTATTCTCTGGCAGATAAAGACGCTCCAATGCTCGCCCAGCCATCCTGGTCTGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:73686626..73686725 26863196 MeRIP-seq:(Medium) rs1554613038 Functional Loss SNV dbSNP153 33..33 33 - - - 88027 RMVar_ID_88027 Human_SNP_ID_326080211 m1A Human chr7 + 73687021 73687021 73687021 TCTAATGTAGATGAGGCTGTGGACCGAGAGATAGAGGGAGACCTGCTGCTGGGGGATATGGGCCA TCTAATGTAGATGAGGCTGTGGACCGAGAGATTGAGGGAGACCTGCTGCTGGGGGATATGGGCCA A T BUD23 Ensembl:ENSG00000071462 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73686880..73687021 26863196 MeRIP-seq:(Medium) rs782289551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792565,Human_RBP_ID_3972009,Human_RBP_ID_4964922,Human_RBP_ID_9354833,Human_RBP_ID_16213627,Human_RBP_ID_19019724,Human_RBP_ID_22464509,Human_RBP_ID_24225633 Human_Splice_Rec_874154,Human_Splice_Rec_874214,Human_Splice_Rec_874215,Human_Splice_Rec_874236,Human_Splice_Rec_874237,Human_Splice_Rec_874248,Human_Splice_Rec_874249,Human_Splice_Rec_874282,Human_Splice_Rec_874283,Human_Splice_Rec_874302,Human_Splice_Rec_874303,Human_Splice_Rec_874324,Human_Splice_Rec_874325,Human_Splice_Rec_874348,Human_Splice_Rec_874349 Human_miRNA_ID_2099484,Human_miRNA_ID_2099485,Human_miRNA_ID_2099486,Human_miRNA_ID_2099487,Human_miRNA_ID_2105439,Human_miRNA_ID_2105440,Human_miRNA_ID_2105441,Human_miRNA_ID_2105442,Human_miRNA_ID_2111383,Human_miRNA_ID_2111384,Human_miRNA_ID_2111385,Human_miRNA_ID_2111386,Human_miRNA_ID_2163930,Human_miRNA_ID_2163931,Human_miRNA_ID_2163932,Human_miRNA_ID_2163933,Human_miRNA_ID_2220940,Human_miRNA_ID_2220941,Human_miRNA_ID_2220942,Human_miRNA_ID_2220943,Human_miRNA_ID_2483987,Human_miRNA_ID_2483988,Human_miRNA_ID_2483989,Human_miRNA_ID_2483990,Human_miRNA_ID_2595156,Human_miRNA_ID_2595157,Human_miRNA_ID_2595158,Human_miRNA_ID_2595159,Human_miRNA_ID_2738099,Human_miRNA_ID_2738100,Human_miRNA_ID_2738101,Human_miRNA_ID_2738102,Human_miRNA_ID_2955509,Human_miRNA_ID_2955510,Human_miRNA_ID_2955511,Human_miRNA_ID_2955512,Human_miRNA_ID_3038697,Human_miRNA_ID_3038698,Human_miRNA_ID_3038699,Human_miRNA_ID_3038700,Human_miRNA_ID_3072364,Human_miRNA_ID_3072365,Human_miRNA_ID_3072366,Human_miRNA_ID_3072367 RMVar_hsa_circ_245593,RMVar_hsa_circ_87453,RMVar_hsa_circ_299918,RMVar_hsa_circ_372258,RMVar_hsa_circ_272645,RMVar_hsa_circ_119564,RMVar_hsa_circ_245595,RMVar_hsa_circ_245596,RMVar_hsa_circ_245594,RMVar_hsa_circ_34847,RMVar_hsa_circ_60048,RMVar_hsa_circ_245592,RMVar_hsa_circ_94878,RMVar_hsa_circ_245598 88028 RMVar_ID_88028 Human_SNP_ID_326081149 m1A Human chr7 + 73690930 73690930 73690930 AGGTCCCTTCCTTTTTAGCATTTCTGCTGTGCAGTGGCTCTGTAATGCTAACAAGAAGTCTGAAA AGGTCCCTTCCTTTTTAGCATTTCTGCTGTGCGGTGGCTCTGTAATGCTAACAAGAAGTCTGAAA A G BUD23 Ensembl:ENSG00000071462 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:73690901..73691025 26863196 MeRIP-seq:(Medium) rs548278021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952523,Human_RBP_ID_1399446,Human_RBP_ID_2046704,Human_RBP_ID_3970946,Human_RBP_ID_16213707,Human_RBP_ID_22464510 Human_Splice_Rec_874162,Human_Splice_Rec_874163,Human_Splice_Rec_874198,Human_Splice_Rec_874199,Human_Splice_Rec_874216,Human_Splice_Rec_874217,Human_Splice_Rec_874238,Human_Splice_Rec_874239,Human_Splice_Rec_874284,Human_Splice_Rec_874285,Human_Splice_Rec_874304,Human_Splice_Rec_874305,Human_Splice_Rec_874326,Human_Splice_Rec_874327,Human_Splice_Rec_874365 RMVar_hsa_circ_245593,RMVar_hsa_circ_87453,RMVar_hsa_circ_299918,RMVar_hsa_circ_372258,RMVar_hsa_circ_119564,RMVar_hsa_circ_245595,RMVar_hsa_circ_245594,RMVar_hsa_circ_34847,RMVar_hsa_circ_60048,RMVar_hsa_circ_245592,RMVar_hsa_circ_94878,RMVar_hsa_circ_112075,RMVar_hsa_circ_122093,RMVar_hsa_circ_245598,RMVar_hsa_circ_245599,RMVar_hsa_circ_245600 88029 RMVar_ID_88029 Human_SNP_ID_326081151 m1A Human chr7 - 73690938 73690938 73690938 GGCAGGGTTTTCAGACTTCTTGTTAGCATTACAGAGCCACTGCACAGCAGAAATGCTAAAAAGGA GGCAGGGTTTTCAGACTTCTTGTTAGCATTACCGAGCCACTGCACAGCAGAAATGCTAAAAAGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73690901..73690975 26863196 MeRIP-seq:(Medium) rs781866736 Functional Loss SNV dbSNP153 33..33 33 - - - 88030 RMVar_ID_88030 Human_SNP_ID_326082010 m1A Human chr7 + 73694044 73694044 73694044 TGAAGTTGAACCCAGGGAGTCTGTGTTCACCAATGAGAGGTAAAGCAACTGCTGAAGCCTGCCCC TGAAGTTGAACCCAGGGAGTCTGTGTTCACCAGTGAGAGGTAAAGCAACTGCTGAAGCCTGCCCC A G BUD23 Ensembl:ENSG00000071462 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73693976..73694075 26863196 MeRIP-seq:(Medium) rs782259467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956449,Human_RBP_ID_5153210,Human_RBP_ID_5403090,Human_RBP_ID_17664273,Human_RBP_ID_19019725,Human_RBP_ID_19134985,Human_RBP_ID_22464513,Human_RBP_ID_22686933 Human_Splice_Rec_874170,Human_Splice_Rec_874184,Human_Splice_Rec_874185,Human_Splice_Rec_874206,Human_Splice_Rec_874224,Human_Splice_Rec_874225,Human_Splice_Rec_874256,Human_Splice_Rec_874270,Human_Splice_Rec_874271,Human_Splice_Rec_874290,Human_Splice_Rec_874291,Human_Splice_Rec_874312,Human_Splice_Rec_874313,Human_Splice_Rec_874334,Human_Splice_Rec_874335,Human_Splice_Rec_874360,Human_Splice_Rec_874361 RMVar_hsa_circ_245593,RMVar_hsa_circ_87453,RMVar_hsa_circ_372258,RMVar_hsa_circ_245592,RMVar_hsa_circ_122093,RMVar_hsa_circ_245600,RMVar_hsa_circ_65098 88031 RMVar_ID_88031 Human_SNP_ID_326082902 m1A Human chr7 + 73697645 73697645 73697645 TAAGGATGTCGAGGCGGGGAATGGTGAGGAAGAGTCGGGCATGGGTGCTGGAGAAGAAGGAGCGG TAAGGATGTCGAGGCGGGGAATGGTGAGGAAGGGTCGGGCATGGGTGCTGGAGAAGAAGGAGCGG A G BUD23 Ensembl:ENSG00000071462 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:73697601..73697700 26863196 MeRIP-seq:(Medium) rs782543202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83001,Human_RBP_ID_253025,Human_RBP_ID_687900,Human_RBP_ID_3970950,Human_RBP_ID_5152953,Human_RBP_ID_9403476,Human_RBP_ID_16213884,Human_RBP_ID_17665017,Human_RBP_ID_18171738,Human_RBP_ID_19020943,Human_RBP_ID_22464514,Human_RBP_ID_22774911,Human_RBP_ID_23140208,Human_RBP_ID_24225667 Human_Splice_Rec_874226,Human_Splice_Rec_874227,Human_Splice_Rec_874272,Human_Splice_Rec_874273,Human_Splice_Rec_874292,Human_Splice_Rec_874293,Human_Splice_Rec_874314,Human_Splice_Rec_874315,Human_Splice_Rec_874338,Human_Splice_Rec_874339,Human_Splice_Rec_874362,Human_Splice_Rec_874363,Human_Splice_Rec_874372,Human_Splice_Rec_874373,Human_Splice_Rec_874376,Human_Splice_Rec_874377,Human_Splice_Rec_874379 Human_miRNA_ID_973567 RMVar_hsa_circ_372258,RMVar_hsa_circ_245592,RMVar_hsa_circ_65098 88032 RMVar_ID_88032 Human_SNP_ID_326082907 m1A Human chr7 - 73697654 73697654 73697654 GCGCCTGTGCCGCTCCTTCTTCTCCAGCACCCATGCCCGACTCTTCCTCACCATTCCCCGCCTCG GCGCCTGTGCCGCTCCTTCTTCTCCAGCACCCGTGCCCGACTCTTCCTCACCATTCCCCGCCTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73697580..73697709 26863196 MeRIP-seq:(Medium) rs782504979 Functional Loss SNV dbSNP153 33..33 33 - - - 88033 RMVar_ID_88033 Human_SNP_ID_326083105 m1A Human chr7 + 73698138 73698137 73698138 GGCAACATAATGAAACTTCCTTTCCAGGGAGGAAAAAAAAAAAAAAAAAAAGCTCTGAGAGCATC GGCAACATAATGAAACTTCCTTTCCAGGGAGG_AAAAAAAAAAAAAAAAAAGCTCTGAGAGCATC GA G BUD23 Ensembl:ENSG00000071462 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11390617 Functional Loss DEL dbSNP153 33..33 33 - - - 88034 RMVar_ID_88034 Human_SNP_ID_326083110 m1A Human chr7 + 73698138 73698138 73698138 GGCAACATAATGAAACTTCCTTTCCAGGGAGGAAAAAAAAAAAAAAAAAAAGCTCTGAGAGCATC GGCAACATAATGAAACTTCCTTTCCAGGGAGGGAAAAAAAAAAAAAAAAAAGCTCTGAGAGCATC A G BUD23 Ensembl:ENSG00000071462 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs797044306 Functional Loss SNV dbSNP153 33..33 33 - - - 88035 RMVar_ID_88035 Human_SNP_ID_326085530 m1A Human chr7 + 73706619 73706619 73706619 GTGCATGACACCGCAGCAGGAGACGGTGCAGGAGGTGGCCTGCAGGAGCCCAAGGTGTGGAGCAG GTGCATGACACCGCAGCAGGAGACGGTGCAGGTGGTGGCCTGCAGGAGCCCAAGGTGTGGAGCAG A T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:73706617..73706780 26863196 MeRIP-seq:(Medium) rs1285357650 Functional Loss SNV dbSNP153 33..33 33 - - - 88036 RMVar_ID_88036 Human_SNP_ID_326093751 m1A Human chr7 + 73736618 73736618 73736618 TATGAAGTCCTGTGGGCGGTCAGCGTGGATCCAGTGGCCAGCGTTCGGCACCGTCTGCATCTGGG TATGAAGTCCTGTGGGCGGTCAGCGTGGATCCGGTGGCCAGCGTTCGGCACCGTCTGCATCTGGG A G NONHSAG047942.2,RF00017-4508 RNACentral:URS00008B7749,RNACentral:URS000093D619 lincRNA,SRP RNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73736571..73736674 26863196 MeRIP-seq:(Medium) rs782161769 Functional Loss SNV dbSNP153 33..33 33 - - - 88037 RMVar_ID_88037 Human_SNP_ID_326094630 m1A Human chr7 - 73738770 73738770 73738770 GTGAGATGCGAGCCGGCCAACAGCTTGCAAGCATGCTCCGCTGGACCCGAGCCTGGAGGCTCCCG GTGAGATGCGAGCCGGCCAACAGCTTGCAAGCGTGCTCCGCTGGACCCGAGCCTGGAGGCTCCCG T C ABHD11 Ensembl:ENSG00000106077 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73738720..73738796 26863196 MeRIP-seq:(Medium) rs782222712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956413,Human_RBP_ID_9404549,Human_RBP_ID_23080322,Human_RBP_ID_27829393 88038 RMVar_ID_88038 Human_SNP_ID_326099465 m1A Human chr7 + 73757532 73757532 73757532 AGCCTATGGTCCAGAGAGTGCAGGGAGAGTGCAGGGTTTTTGAGGAGAGAAAGGATGTCGAGTGG AGCCTATGGTCCAGAGAGTGCAGGGAGAGTGCGGGGTTTTTGAGGAGAGAAAGGATGTCGAGTGG A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:73757460..73757679 26863196 MeRIP-seq:(Medium) rs545936356 Functional Loss SNV dbSNP153 33..33 33 - - - 88039 RMVar_ID_88039 Human_SNP_ID_326184667 m1A Human chr7 + 74083816 74083816 74083816 CCGCCTCGGTCCGCCCCTCCGCTCGCTCCCCAAGCCGCCGCGGCGCCGAGCCGGTTTCCCCGCCG CCGCCTCGGTCCGCCCCTCCGCTCGCTCCCCAGGCCGCCGCGGCGCCGAGCCGGTTTCCCCGCCG A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:74083801..74083987 26863196 MeRIP-seq:(Medium) rs1554693656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110007,RMVar_hsa_circ_122578,RMVar_hsa_circ_245612,RMVar_hsa_circ_245613 88040 RMVar_ID_88040 Human_SNP_ID_326184703 m1A Human chr7 - 74083894 74083894 74083894 CCACCGCCGCCGGCCCGGGGAGGCGGGGGCGGAGGGCGCGGGCCGGGCCGGGCCGGGCCGGGGGC CCACCGCCGCCGGCCCGGGGAGGCGGGGGCGGGGGGCGCGGGCCGGGCCGGGCCGGGCCGGGGGC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:74083801..74083975 26863410 MeRIP-seq:(Medium) rs1554693686 Functional Loss SNV dbSNP153 33..33 33 - - - 88041 RMVar_ID_88041 Human_SNP_ID_326184726 m1A Human chr7 + 74083953 74083953 74083953 CGGTGGGCGAGCTCGCGGGCCCGGCCGCCCCCAGCCCCAGCCCCGCCGGGCCCCGCCCCCCGTCG CGGTGGGCGAGCTCGCGGGCCCGGCCGCCCCCCGCCCCAGCCCCGCCGGGCCCCGCCCCCCGTCG A C LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:74083829..74083956 26863196 MeRIP-seq:(Medium) rs1402366146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955815 Human_Splice_Rec_875837,Human_Splice_Rec_875867 Human_miRNA_ID_885906,Human_miRNA_ID_2146413,Human_miRNA_ID_2146414,Human_miRNA_ID_2146415,Human_miRNA_ID_2683956,Human_miRNA_ID_2683957,Human_miRNA_ID_2683958,Human_miRNA_ID_3021539,Human_miRNA_ID_3021540,Human_miRNA_ID_3021541,Human_miRNA_ID_3065657,Human_miRNA_ID_3065658,Human_miRNA_ID_3065659 RMVar_hsa_circ_110007,RMVar_hsa_circ_122578,RMVar_hsa_circ_245612,RMVar_hsa_circ_245613 88042 RMVar_ID_88042 Human_SNP_ID_326186211 m1A Human chr7 - 74089675 74089675 74089675 TAGCCCATGTCCCCTCCAGCTCAACACAGATGAGCATGTCTCCTCCCCAACATGACCCCCAATTC TAGCCCATGTCCCCTCCAGCTCAACACAGATGGGCATGTCTCCTCCCCAACATGACCCCCAATTC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74089671..74090037 26863196 MeRIP-seq:(Medium) rs1351593754 Functional Loss SNV dbSNP153 33..33 33 - - - 88043 RMVar_ID_88043 Human_SNP_ID_326194823 m1A Human chr7 + 74121248 74121248 74121248 AGCTGGAGCAGCTGGACAGAGGTTTCTGGGAGACCTACCGGCGCGGCGAGAGCGGACTGCCTGCC AGCTGGAGCAGCTGGACAGAGGTTTCTGGGAGGCCTACCGGCGCGGCGAGAGCGGACTGCCTGCC A G LIMK1 Ensembl:ENSG00000106683 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:74121119..74121307 26863196 MeRIP-seq:(Medium) rs782588250 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1052878,Human_RBP_ID_7757129 RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_98103,RMVar_hsa_circ_245622,RMVar_hsa_circ_264877 88044 RMVar_ID_88044 Human_SNP_ID_326195124 m1A Human chr7 + 74122226 74122226 74122226 TGCGTTTTTTCTGTGTAATCTATTTTTTAAGAAGAGTTTGTATTATTTTTTCATACGGCTGCAGC TGCGTTTTTTCTGTGTAATCTATTTTTTAAGAGGAGTTTGTATTATTTTTTCATACGGCTGCAGC A G LIMK1 Ensembl:ENSG00000106683 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:74122176..74122277 32194978 MeRIP-seq:(Medium) rs1312979174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2046719,Human_RBP_ID_3852341,Human_RBP_ID_21904065 Human_miRNA_ID_2507654,Human_miRNA_ID_2507655,Human_miRNA_ID_2507656,Human_miRNA_ID_2532255,Human_miRNA_ID_2532256,Human_miRNA_ID_2532257,Human_miRNA_ID_2983343,Human_miRNA_ID_2983344,Human_miRNA_ID_2983345 RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_98103,RMVar_hsa_circ_245622 88045 RMVar_ID_88045 Human_SNP_ID_326208958 m1A Human chr7 + 74174399 74174399 74174399 CGGAGCGGAGACGGCAAATGGCGGACTTCGACACCTACGACGATCGGGCCTACAGCAGCTTCGGC CGGAGCGGAGACGGCAAATGGCGGACTTCGACGCCTACGACGATCGGGCCTACAGCAGCTTCGGC A G EIF4H Ensembl:ENSG00000106682 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:74174351..74174568 26863196 MeRIP-seq:(Medium) rs1441368382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253268,Human_RBP_ID_687950,Human_RBP_ID_1688632,Human_RBP_ID_2046720,Human_RBP_ID_4956414,Human_RBP_ID_5623051,Human_RBP_ID_7757150,Human_RBP_ID_8912557,Human_RBP_ID_9337183,Human_RBP_ID_16214132,Human_RBP_ID_22464024 Human_Splice_Rec_875953,Human_Splice_Rec_875965,Human_Splice_Rec_875971,Human_Splice_Rec_875981 RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 88046 RMVar_ID_88046 Human_SNP_ID_326208969 m1A Human chr7 - 74174427 74174427 74174427 GCGCACGCCCGCCTCACCCTCTGCCGCCGCCGAAGCTGCTGTAGGCCCGATCGTCGTAGGTGTCG GCGCACGCCCGCCTCACCCTCTGCCGCCGCCGGAGCTGCTGTAGGCCCGATCGTCGTAGGTGTCG T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr7:74174376..74174450;chr7:74174344..74183823 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 88047 RMVar_ID_88047 Human_SNP_ID_326213237 m1A Human chr7 - 74190229 74190228 74190230 GAGAGCTACCCATTCCTGAGGATACACAAAAAAGATAAAGTTGAGGTCGTGTCATTACCTTGCTG GAGAGCTACCCATTCCTGAGGATACACAAAA__GATAAAGTTGAGGTCGTGTCATTACCTTGCTG CTT C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:74190226..74190275;chr7:74190226..74190325;chr7:74190226..74190300 26863196 MeRIP-seq:(Medium) rs781997743 Functional Loss DEL dbSNP153 32..33 33 - - - 88048 RMVar_ID_88048 Human_SNP_ID_326213239 m1A Human chr7 - 74190229 74190229 74190229 GAGAGCTACCCATTCCTGAGGATACACAAAAAAGATAAAGTTGAGGTCGTGTCATTACCTTGCTG GAGAGCTACCCATTCCTGAGGATACACAAAAAGGATAAAGTTGAGGTCGTGTCATTACCTTGCTG T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:74190226..74190275;chr7:74190226..74190325;chr7:74190226..74190300 26863196 MeRIP-seq:(Medium) rs368681152 Functional Loss SNV dbSNP153 33..33 33 - - - 88049 RMVar_ID_88049 Human_SNP_ID_326214610 m1A Human chr7 - 74194840 74194837 74194840 TGGGTTCTCTGAAATCCATGTTGGATCCACGGAGGGGAGGGCCATCTCTGAAGCGGCTGCCCATG TGGGTTCTCTGAAATCCATGTTGGATCCACGG___GGAGGGCCATCTCTGAAGCGGCTGCCCATG CCCT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:74194776..74195257;chr7:74194776..74194900 32194978 MeRIP-seq:(Medium) rs1274820067 Functional Loss DEL dbSNP153 33..35 33 - - - 88050 RMVar_ID_88050 Human_SNP_ID_326214614 m1A Human chr7 - 74194848 74194848 74194848 ACCTTCTGTGGGTTCTCTGAAATCCATGTTGGATCCACGGAGGGGAGGGCCATCTCTGAAGCGGC ACCTTCTGTGGGTTCTCTGAAATCCATGTTGGGTCCACGGAGGGGAGGGCCATCTCTGAAGCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:74194797..74194922 26863196 MeRIP-seq:(Medium) rs1554710477 Functional Loss SNV dbSNP153 33..33 33 - - - 88051 RMVar_ID_88051 Human_SNP_ID_326214848 m1A Human chr7 - 74195596 74195596 74195596 CGGCGGCCACCTCTGCTCCTCCGAGGAACCCCATGTGCTGCTGGGAAAACAAGGAGCAGGAGAAA CGGCGGCCACCTCTGCTCCTCCGAGGAACCCCGTGTGCTGCTGGGAAAACAAGGAGCAGGAGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:74195551..74195650 32194978 MeRIP-seq:(Medium) rs562848775 Functional Loss SNV dbSNP153 33..33 33 - - - 88052 RMVar_ID_88052 Human_SNP_ID_326215010 m1A Human chr7 - 74196120 74196118 74196120 ACCCGCTGGCCATTCACTGCACCCAGCCAGAGAGGCCAGCCTCCACCACGCACGGCGAAAGGAGT ACCCGCTGGCCATTCACTGCACCCAGCCAGAG__GCCAGCCTCCACCACGCACGGCGAAAGGAGT CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:74195971..74196260 26863196 MeRIP-seq:(Medium) rs1304402390 Functional Loss DEL dbSNP153 33..34 33 - - - 88053 RMVar_ID_88053 Human_SNP_ID_326231181 m1A Human chr7 - 74250611 74250609 74250612 GGATGGAGAGAAGTAAAGGACGCTGGAGACGAAGGAGGAGGATGGTGAAGCCCTGGTTATTGAAG GGATGGAGAGAAGTAAAGGACGCTGGAGACG___GAGGAGGATGGTGAAGCCCTGGTTATTGAAG CCTT C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74250607..74250741 26863196 MeRIP-seq:(Medium) rs1465109746 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_118181,RMVar_hsa_circ_315698,RMVar_hsa_circ_245653,RMVar_hsa_circ_265389,RMVar_hsa_circ_344571,RMVar_hsa_circ_245661 88054 RMVar_ID_88054 Human_SNP_ID_326231783 m1A Human chr7 - 74252485 74252485 74252485 TTATGCATTTTCTTAACAGGGTTGAAAAATATAGGCCAGTAAAGCTGAATGAAATTGTCGGGAAT TTATGCATTTTCTTAACAGGGTTGAAAAATATGGGCCAGTAAAGCTGAATGAAATTGTCGGGAAT T C RFC2 Ensembl:ENSG00000049541 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74252426..74252548 26863196 MeRIP-seq:(Medium) rs1554721319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2046775,Human_RBP_ID_16216000 Human_Splice_Rec_876182,Human_Splice_Rec_876183,Human_Splice_Rec_876200,Human_Splice_Rec_876201,Human_Splice_Rec_876220,Human_Splice_Rec_876221,Human_Splice_Rec_876258,Human_Splice_Rec_876259,Human_Splice_Rec_876274,Human_Splice_Rec_876275,Human_Splice_Rec_876288,Human_Splice_Rec_876289,Human_Splice_Rec_876304,Human_Splice_Rec_876305,Human_Splice_Rec_876319,Human_Splice_Rec_876335,Human_Splice_Rec_876346,Human_Splice_Rec_876347 Human_miRNA_ID_2155508,Human_miRNA_ID_2155509,Human_miRNA_ID_2155510,Human_miRNA_ID_2159070,Human_miRNA_ID_2159071,Human_miRNA_ID_2159072 RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_118181,RMVar_hsa_circ_315698,RMVar_hsa_circ_245653,RMVar_hsa_circ_265389,RMVar_hsa_circ_344571,RMVar_hsa_circ_245661 88055 RMVar_ID_88055 Human_SNP_ID_326231787 m1A Human chr7 - 74252493 74252493 74252493 CAGCATTTTTATGCATTTTCTTAACAGGGTTGAAAAATATAGGCCAGTAAAGCTGAATGAAATTG CAGCATTTTTATGCATTTTCTTAACAGGGTTGGAAAATATAGGCCAGTAAAGCTGAATGAAATTG T C RFC2 Ensembl:ENSG00000049541 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:74252426..74252565 26863410 MeRIP-seq:(Medium) rs782396570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_876182,Human_Splice_Rec_876183,Human_Splice_Rec_876200,Human_Splice_Rec_876201,Human_Splice_Rec_876220,Human_Splice_Rec_876221,Human_Splice_Rec_876258,Human_Splice_Rec_876259,Human_Splice_Rec_876274,Human_Splice_Rec_876275,Human_Splice_Rec_876288,Human_Splice_Rec_876289,Human_Splice_Rec_876304,Human_Splice_Rec_876305,Human_Splice_Rec_876319,Human_Splice_Rec_876335,Human_Splice_Rec_876346,Human_Splice_Rec_876347 Human_miRNA_ID_2155508,Human_miRNA_ID_2155509,Human_miRNA_ID_2155510,Human_miRNA_ID_2159070,Human_miRNA_ID_2159071,Human_miRNA_ID_2159072 RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_118181,RMVar_hsa_circ_315698,RMVar_hsa_circ_245653,RMVar_hsa_circ_265389,RMVar_hsa_circ_344571,RMVar_hsa_circ_245661 88056 RMVar_ID_88056 Human_SNP_ID_326232269 m1A Human chr7 - 74254311 74254311 74254311 AGGCCCAGGACTCTGACCCTGCCCCTGCCTTCAGCAAGGCCCCCGGCAGCGCCGGCCACTACGAA AGGCCCAGGACTCTGACCCTGCCCCTGCCTTCGGCAAGGCCCCCGGCAGCGCCGGCCACTACGAA T C RFC2 Ensembl:ENSG00000049541 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:74254276..74254375 32194978 MeRIP-seq:(Medium) rs1000134831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688011,Human_RBP_ID_4956416,Human_RBP_ID_5327878,Human_RBP_ID_18426031,Human_RBP_ID_19020951,Human_RBP_ID_22464520,Human_RBP_ID_23215535,Human_RBP_ID_26356561 Human_Splice_Rec_876181,Human_Splice_Rec_876199,Human_Splice_Rec_876219,Human_Splice_Rec_876257,Human_Splice_Rec_876273,Human_Splice_Rec_876287,Human_Splice_Rec_876303,Human_Splice_Rec_876333,Human_Splice_Rec_876345,Human_Splice_Rec_876359 RMVar_hsa_circ_118181,RMVar_hsa_circ_245653 88057 RMVar_ID_88057 Human_SNP_ID_326232299 m1A Human chr7 + 74254367 74254365 74254368 CCTGGGCCTCCACCTCGCCCGCGCCACCACAGACGGCCTCCACCTCCATTCTCGCGCCTCCTCTT CCTGGGCCTCCACCTCGCCCGCGCCACCACA___GGCCTCCACCTCCATTCTCGCGCCTCCTCTT AGAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74254114..74254425 26863196 MeRIP-seq:(Medium) rs1564004183 Functional Loss DEL dbSNP153 32..34 33 - - - 88058 RMVar_ID_88058 Human_SNP_ID_326232300 m1A Human chr7 + 74254365 74254365 74254365 GTCCTGGGCCTCCACCTCGCCCGCGCCACCACAGACGGCCTCCACCTCCATTCTCGCGCCTCCTC GTCCTGGGCCTCCACCTCGCCCGCGCCACCACCGACGGCCTCCACCTCCATTCTCGCGCCTCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:74254223..74254425;chr7:74254239..74254401;chr7:74254180..74254425;chr7:74249812..74254425 26863196 MeRIP-seq:(Medium) rs1168067660 Functional Loss SNV dbSNP153 33..33 33 - - - 88059 RMVar_ID_88059 Human_SNP_ID_326232301 m1A Human chr7 + 74254365 74254365 74254365 GTCCTGGGCCTCCACCTCGCCCGCGCCACCACAGACGGCCTCCACCTCCATTCTCGCGCCTCCTC GTCCTGGGCCTCCACCTCGCCCGCGCCACCACGGACGGCCTCCACCTCCATTCTCGCGCCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:74254223..74254425;chr7:74254239..74254401;chr7:74254180..74254425;chr7:74249812..74254425 26863196 MeRIP-seq:(Medium) rs1168067660 Functional Loss SNV dbSNP153 33..33 33 - - - 88060 RMVar_ID_88060 Human_SNP_ID_326241937 m1A Human chr7 - 74289722 74289722 74289722 GCCCCTCCAGCAGCCCCTACCTTCGTCCTTCCAGCATCAGGCTAAGCGGCGGGAGGCCCGGAGAG GCCCCTCCAGCAGCCCCTACCTTCGTCCTTCCGGCATCAGGCTAAGCGGCGGGAGGCCCGGAGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74289463..74289751 26863196 MeRIP-seq:(Medium) rs551677408 Functional Loss SNV dbSNP153 33..33 33 - - - 88061 RMVar_ID_88061 Human_SNP_ID_326258293 m1A Human chr7 + 74350923 74350914 74350923 AAGGAAGGAAGAAAGGAAGGAAAGGGAAGGGAAGGAAGGGAAGGAAAGGAAGGAAGGGAAAGAAA AAGGAAGGAAGAAAGGAAGGAAAG_________GGAAGGGAAGGAAAGGAAGGAAGGGAAAGAAA GGGAAGGGAA G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74350909..74351180 26863196 MeRIP-seq:(Medium) rs199529714 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_211,RMVar_hsa_circ_92919,RMVar_hsa_circ_245662,RMVar_hsa_circ_333961,RMVar_hsa_circ_107546,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_343656,RMVar_hsa_circ_245668,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_292121,RMVar_hsa_circ_299528,RMVar_hsa_circ_26978,RMVar_hsa_circ_83371,RMVar_hsa_circ_245673,RMVar_hsa_circ_245675,RMVar_hsa_circ_245674,RMVar_hsa_circ_245672,RMVar_hsa_circ_245670 88062 RMVar_ID_88062 Human_SNP_ID_326265639 m1A Human chr7 + 74376682 74376679 74376682 AGTTCCTCAAGGAGCAGATCTCGCTGGCCGAGAAGAAGATGTTGGACTACGAGCGGCTGCAGCGG AGTTCCTCAAGGAGCAGATCTCGCTGGCCG___AGAAGATGTTGGACTACGAGCGGCTGCAGCGG GAGA G CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74376632..74376749 26863196 MeRIP-seq:(Medium) rs1273300405 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_9403479 RMVar_hsa_circ_107546,RMVar_hsa_circ_2528,RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_83371,RMVar_hsa_circ_245672,RMVar_hsa_circ_103650,RMVar_hsa_circ_245670,RMVar_hsa_circ_245679,RMVar_hsa_circ_372481,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245685,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_8106,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245693,RMVar_hsa_circ_103611,RMVar_hsa_circ_282092,RMVar_hsa_circ_313787,RMVar_hsa_circ_245694,RMVar_hsa_circ_245692 88063 RMVar_ID_88063 Human_SNP_ID_326265640 m1A Human chr7 + 74376682 74376682 74376682 AGTTCCTCAAGGAGCAGATCTCGCTGGCCGAGAAGAAGATGTTGGACTACGAGCGGCTGCAGCGG AGTTCCTCAAGGAGCAGATCTCGCTGGCCGAGTAGAAGATGTTGGACTACGAGCGGCTGCAGCGG A T CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74376632..74376749 26863196 MeRIP-seq:(Medium) rs1215482907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9403479 RMVar_hsa_circ_107546,RMVar_hsa_circ_2528,RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_83371,RMVar_hsa_circ_245672,RMVar_hsa_circ_103650,RMVar_hsa_circ_245670,RMVar_hsa_circ_245679,RMVar_hsa_circ_372481,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245685,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_8106,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245693,RMVar_hsa_circ_103611,RMVar_hsa_circ_282092,RMVar_hsa_circ_313787,RMVar_hsa_circ_245694,RMVar_hsa_circ_245692 88064 RMVar_ID_88064 Human_SNP_ID_326273407 m1A Human chr7 + 74404698 74404694 74404698 AGTGGAGGCTCTAGGCAGGTTTGACAAAGGTCAGTAATACGGTTTCCCCTGGGGTTGACCAGATG AGTGGAGGCTCTAGGCAGGTTTGACAAAG____GTAATACGGTTTCCCCTGGGGTTGACCAGATG GGTCA G CLIP2 Ensembl:ENSG00000106665 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:74404648..74404749 32194978 MeRIP-seq:(Medium) rs1562736629 Functional Loss DEL dbSNP153 30..33 33 - - - 88065 RMVar_ID_88065 Human_SNP_ID_326286572 m1A Human chr7 - 74453991 74453991 74453991 AGGGAGGCGCGGGGAGGGGGCGCGGGGGGGGAATCGGCCGGCCGGGGGGCTGGCGCTCGGCGGCC AGGGAGGCGCGGGGAGGGGGCGCGGGGGGGGAGTCGGCCGGCCGGGGGGCTGGCGCTCGGCGGCC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:74453901..74454050 26863410 MeRIP-seq:(Medium) rs1324421841 Functional Loss SNV dbSNP153 33..33 33 - - - 88066 RMVar_ID_88066 Human_SNP_ID_326286642 m1A Human chr7 + 74454156 74454156 74454156 CCGCGGGCCGGGGCCGGGGCGCCGCTGGCAGGAGCGCTTGGGGATCCTCCAAGGTAGGAGAAACT CCGCGGGCCGGGGCCGGGGCGCCGCTGGCAGGGGCGCTTGGGGATCCTCCAAGGTAGGAGAAACT A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:74454106..74454215 26863196 MeRIP-seq:(Medium) rs1229809585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955823,Human_RBP_ID_5479815,Human_RBP_ID_9311312 Human_Splice_Rec_876451,Human_Splice_Rec_876503,Human_Splice_Rec_876555 88067 RMVar_ID_88067 Human_SNP_ID_326286994 m1A Human chr7 - 74455202 74455201 74455203 ATTCTCCATCCAAGAGTCAGTGCTCCCCTCACAGGCCCTGCAGCGAGACCCCTATGTCCCAGCAC ATTCTCCATCCAAGAGTCAGTGCTCCCCTCA__GGCCCTGCAGCGAGACCCCTATGTCCCAGCAC CTG C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74455200..74455620 26863196 MeRIP-seq:(Medium) rs555870752 Functional Loss DEL dbSNP153 32..33 33 - - - 88068 RMVar_ID_88068 Human_SNP_ID_326287062 m1A Human chr7 + 74455506 74455506 74455506 AAGCAGCTCATTTATTTCAGCAGTGTCATTCCAGAGGGGAAGGGCACCAGCATCGATTATTTATT AAGCAGCTCATTTATTTCAGCAGTGTCATTCCGGAGGGGAAGGGCACCAGCATCGATTATTTATT A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:74455322..74455542 26863196 MeRIP-seq:(Medium) rs1554326995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2051233,Human_miRNA_ID_2051234 88069 RMVar_ID_88069 Human_SNP_ID_326287733 m1A Human chr7 - 74458209 74458209 74458209 GTCACACTAAGGGTCCCTGTCCTAGCGGCCCCATATTATCCCGGAAGCCCCCCAATCAAAACTGA GTCACACTAAGGGTCCCTGTCCTAGCGGCCCCGTATTATCCCGGAAGCCCCCCAATCAAAACTGA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74458208..74458380 26863196 MeRIP-seq:(Medium) rs1002841231 Functional Loss SNV dbSNP153 33..33 33 - - - 88070 RMVar_ID_88070 Human_SNP_ID_326287734 m1A Human chr7 - 74458209 74458209 74458209 GTCACACTAAGGGTCCCTGTCCTAGCGGCCCCATATTATCCCGGAAGCCCCCCAATCAAAACTGA GTCACACTAAGGGTCCCTGTCCTAGCGGCCCCCTATTATCCCGGAAGCCCCCCAATCAAAACTGA T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74458208..74458380 26863196 MeRIP-seq:(Medium) rs1002841231 Functional Loss SNV dbSNP153 33..33 33 - - - 88071 RMVar_ID_88071 Human_SNP_ID_326288483 m1A Human chr7 + 74461144 74461144 74461144 GACTTGGTGTGACCCCGTGGGGATGCCACAGCATGGGTGTGTGGGACCCCCGGGGGCAGGTCTGT GACTTGGTGTGACCCCGTGGGGATGCCACAGCTTGGGTGTGTGGGACCCCCGGGGGCAGGTCTGT A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:74461138..74461254 26863196 MeRIP-seq:(Medium) rs1204951321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21992444 Human_miRNA_ID_2428629,Human_miRNA_ID_2428630,Human_miRNA_ID_2488427,Human_miRNA_ID_2488428 88072 RMVar_ID_88072 Human_SNP_ID_326297477 m1A Human chr7 - 74496534 74496534 74496534 TGTACACCCCCCAAACGCACACACCCACACATACATGCACACCCACACACGCACACCCACATGAA TGTACACCCCCCAAACGCACACACCCACACATGCATGCACACCCACACACGCACACCCACATGAA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:74496268..74496676 26863196 MeRIP-seq:(Medium) rs1304313976 Functional Loss SNV dbSNP153 33..33 33 - - - 88073 RMVar_ID_88073 Human_SNP_ID_326298211 m1A Human chr7 + 74499400 74499396 74499400 CTGAGGGTTCAAAAGTGTGCAAGGAAGGGAGGAAGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG CTGAGGGTTCAAAAGTGTGCAAGGAAGGG____AGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG GAGGA G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74499396..74499588 26863196 MeRIP-seq:(Medium) rs1426312605 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3099811,Human_RBP_ID_24226026 88074 RMVar_ID_88074 Human_SNP_ID_326298213 m1A Human chr7 + 74499400 74499400 74499400 CTGAGGGTTCAAAAGTGTGCAAGGAAGGGAGGAAGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG CTGAGGGTTCAAAAGTGTGCAAGGAAGGGAGGGAGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74499396..74499588 26863196 MeRIP-seq:(Medium) rs10224601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3099811,Human_RBP_ID_24226026 88075 RMVar_ID_88075 Human_SNP_ID_326303444 m1A Human chr7 - 74519519 74519519 74519519 AGGTGGCGGTTGGGGGCAGGTCCTGGGGTGGCACCTTGGGGGCCTGGCCATGCAGGCCACAGTCC AGGTGGCGGTTGGGGGCAGGTCCTGGGGTGGCTCCTTGGGGGCCTGGCCATGCAGGCCACAGTCC T A RF00017-049,RF00017-4503 RNACentral:URS000096B6E3,RNACentral:URS00009569F7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74519470..74519654 26863196 MeRIP-seq:(Medium) rs782175403 Functional Loss SNV dbSNP153 33..33 33 - - - 88076 RMVar_ID_88076 Human_SNP_ID_326303460 m1A Human chr7 + 74519576 74519564 74519576 CGCCACCTCCTCCTCCATGGCCAGCTTCCTGTACAGCACGGCGCTCCCCAACCACGCCATCCGAG CGCCACCTCCTCCTCCATGGC____________CAGCACGGCGCTCCCCAACCACGCCATCCGAG CCAGCTTCCTGTA C GTF2IRD1 Ensembl:ENSG00000006704 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:74519485..74519660 26863196 MeRIP-seq:(Medium) rs1554345416 Functional Loss DEL dbSNP153 22..33 33 - - - Human_miRNA_ID_2366729,Human_miRNA_ID_2366730,Human_miRNA_ID_2366731 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_362684,RMVar_hsa_circ_372103,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_23959,RMVar_hsa_circ_245704,RMVar_hsa_circ_245705,RMVar_hsa_circ_245703,RMVar_hsa_circ_245707,RMVar_hsa_circ_373383 88077 RMVar_ID_88077 Human_SNP_ID_326303499 m1A Human chr7 + 74519651 74519651 74519651 GGAAGCACCTTCCTGCCCCCTTGCCCCCAGCGACCTGGGCCTGAGTCGGCCCATGCCAGAGCCCA GGAAGCACCTTCCTGCCCCCTTGCCCCCAGCGGCCTGGGCCTGAGTCGGCCCATGCCAGAGCCCA A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:74519626..74519650 26863196 MeRIP-seq:(Medium) rs1554345468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_688026 Human_Splice_Rec_876461,Human_Splice_Rec_876513,Human_Splice_Rec_876565,Human_Splice_Rec_876617,Human_Splice_Rec_876665 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_362684,RMVar_hsa_circ_372103,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_23959,RMVar_hsa_circ_245704,RMVar_hsa_circ_245705,RMVar_hsa_circ_245703,RMVar_hsa_circ_245707,RMVar_hsa_circ_373383 88078 RMVar_ID_88078 Human_SNP_ID_326305968 m1A Human chr7 - 74528996 74528996 74528996 ATCCATCAGTCCGTCTATCCATCCATCCATCCATCCGTCTATCCATCCATCCATCCATCCATCCA ATCCATCAGTCCGTCTATCCATCCATCCATCCGTCCGTCTATCCATCCATCCATCCATCCATCCA T C RF00017-049,RF00017-4503 RNACentral:URS000096B6E3,RNACentral:URS00009569F7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:74528980..74529074 26863196 MeRIP-seq:(Medium) rs782420480 Functional Loss SNV dbSNP153 33..33 33 - - - 88079 RMVar_ID_88079 Human_SNP_ID_326308723 m1A Human chr7 + 74539967 74539967 74539967 GAGGATTCTGGTTATGGGATGGAGATGCTGACAGGTAAGAAATGGACCTGGGCTGGTGGTGCTTG GAGGATTCTGGTTATGGGATGGAGATGCTGACTGGTAAGAAATGGACCTGGGCTGGTGGTGCTTG A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74539954..74540027 26863196 MeRIP-seq:(Medium) rs782162912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19020970,Human_RBP_ID_19136578 Human_Splice_Rec_876476,Human_Splice_Rec_876477,Human_Splice_Rec_876528,Human_Splice_Rec_876529,Human_Splice_Rec_876580,Human_Splice_Rec_876581,Human_Splice_Rec_876632,Human_Splice_Rec_876633,Human_Splice_Rec_876680,Human_Splice_Rec_876681 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245705,RMVar_hsa_circ_82916,RMVar_hsa_circ_245707,RMVar_hsa_circ_373383,RMVar_hsa_circ_332484,RMVar_hsa_circ_13887,RMVar_hsa_circ_107114,RMVar_hsa_circ_245709,RMVar_hsa_circ_245708,RMVar_hsa_circ_332852,RMVar_hsa_circ_88326,RMVar_hsa_circ_245712,RMVar_hsa_circ_245711,RMVar_hsa_circ_372318,RMVar_hsa_circ_26603,RMVar_hsa_circ_323052,RMVar_hsa_circ_290697,RMVar_hsa_circ_245713 88080 RMVar_ID_88080 Human_SNP_ID_326313986 m1A Human chr7 + 74561615 74561615 74561615 TTCCGGAGCTCTCGGAGGGGCAGAGTGGTCAGATGATGTTGGAAAGGTGGAGAGAGTGGAAGCTG TTCCGGAGCTCTCGGAGGGGCAGAGTGGTCAGGTGATGTTGGAAAGGTGGAGAGAGTGGAAGCTG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74561321..74561718 26863196 MeRIP-seq:(Medium) rs1554359105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_29785,RMVar_hsa_circ_13882,RMVar_hsa_circ_13887,RMVar_hsa_circ_21232,RMVar_hsa_circ_343619 88081 RMVar_ID_88081 Human_SNP_ID_326320121 m1A Human chr7 - 74586417 74586417 74586417 CATTCCAGACAACGTCCTCCTCCCGTGTCCCTATCTCGTGGAGTAATGCCTCTAATTCAGCCACA CATTCCAGACAACGTCCTCCTCCCGTGTCCCTGTCTCGTGGAGTAATGCCTCTAATTCAGCCACA T C RF00017-049,RF00017-4503 RNACentral:URS000096B6E3,RNACentral:URS00009569F7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74586413..74586581 26863196 MeRIP-seq:(Medium) rs1234569407 Functional Loss SNV dbSNP153 33..33 33 - - - 88082 RMVar_ID_88082 Human_SNP_ID_326320358 m1A Human chr7 - 74587505 74587505 74587505 AGGCAGGGAGCCAGGGCCGGATGATTCAGGGCAGAGCAGACTGATGGGTCTTTGGAGCAAAATGA AGGCAGGGAGCCAGGGCCGGATGATTCAGGGCGGAGCAGACTGATGGGTCTTTGGAGCAAAATGA T C RF00017-049,RF00017-4503 RNACentral:URS000096B6E3,RNACentral:URS00009569F7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74587503..74587705 26863196 MeRIP-seq:(Medium) rs1255814253 Functional Loss SNV dbSNP153 33..33 33 - - - 88083 RMVar_ID_88083 Human_SNP_ID_326385160 m1A Human chr7 - 74880318 74880318 74880318 ACGAGGTCTTGCTTTGTTTTCCAGGCTGGAGTACAGTGGCTCAATCATAGCTCACTGCAGCCTCA ACGAGGTCTTGCTTTGTTTTCCAGGCTGGAGTCCAGTGGCTCAATCATAGCTCACTGCAGCCTCA T G STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1438584733 Functional Loss SNV dbSNP153 33..33 33 - - - 88084 RMVar_ID_88084 Human_SNP_ID_326387827 m1A Human chr7 + 74890513 74890513 74890513 CGCCAGACACCAACGCTCGGAAACCGCCAGACACCAACGCTCGGAATACACGCCAGACCACGACG CGCCAGACACCAACGCTCGGAAACCGCCAGACGCCAACGCTCGGAATACACGCCAGACCACGACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74890462..74890527 26863196 MeRIP-seq:(Medium) rs1433520186 Functional Loss SNV dbSNP153 33..33 33 - - - 88085 RMVar_ID_88085 Human_SNP_ID_326388019 m1A Human chr7 - 74890853 74890853 74890853 AGAGGGCGCGCGAGAGGGGCGACCGCGAGCCCAGCTCACCTCCAGCTCTCAGCTCTCTCCAAGGA AGAGGGCGCGCGAGAGGGGCGACCGCGAGCCCTGCTCACCTCCAGCTCTCAGCTCTCTCCAAGGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74890833..74890968 26863196 MeRIP-seq:(Medium) rs782005060 Functional Loss SNV dbSNP153 33..33 33 - - - 88086 RMVar_ID_88086 Human_SNP_ID_326388020 m1A Human chr7 - 74890853 74890853 74890853 AGAGGGCGCGCGAGAGGGGCGACCGCGAGCCCAGCTCACCTCCAGCTCTCAGCTCTCTCCAAGGA AGAGGGCGCGCGAGAGGGGCGACCGCGAGCCCCGCTCACCTCCAGCTCTCAGCTCTCTCCAAGGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:74890833..74890968 26863196 MeRIP-seq:(Medium) rs782005060 Functional Loss SNV dbSNP153 33..33 33 - - - 88087 RMVar_ID_88087 Human_SNP_ID_326408585 m1A Human chr7 + 74991740 74991740 74991740 TCAACCCTAAGACCTGAAGGCTGGGGAGTGGAATGAGGGTCCCGGGGGAGGATATGGCACACTAA TCAACCCTAAGACCTGAAGGCTGGGGAGTGGAGTGAGGGTCCCGGGGGAGGATATGGCACACTAA A G CASTOR2 Ensembl:ENSG00000274070 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74991690..74991837 26863196 MeRIP-seq:(Medium) rs1424039822 Functional Loss SNV dbSNP153 33..33 33 - - - 88088 RMVar_ID_88088 Human_SNP_ID_8138168 m1A Human chr1 + 30869783 30869783 30869783 GAGGGAATGGCAGACCCCCACCCACCCCAGGCAGGTTCTGTACAGGAGAAAGGACTCACAGGAGG GAGGGAATGGCAGACCCCCACCCACCCCAGGCTGGTTCTGTACAGGAGAAAGGACTCACAGGAGG A T lnc-ZCCHC17-10 RNACentral:URS00008B34A4 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:30869746..30869959 26863196 MeRIP-seq:(Medium) rs1160706370 Functional Loss SNV dbSNP153 33..33 33 - - - 88089 RMVar_ID_88089 Human_SNP_ID_8162878 m1A Human chr1 + 30964910 30964910 30964910 GGCGGGAGCCACTGCCAGTGTTGGAGTTTGCAACTAAAATGGAATTAAAACAATGCAGATAAGAA GGCGGGAGCCACTGCCAGTGTTGGAGTTTGCAGCTAAAATGGAATTAAAACAATGCAGATAAGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:30964883..30966105 32194978 MeRIP-seq:(Medium) rs749551152 Functional Loss SNV dbSNP153 33..33 33 - - - 88090 RMVar_ID_88090 Human_SNP_ID_8187168 m1A Human chr1 + 31059239 31059239 31059239 ATGTTCTGCATGAATGTTATCCCCAGTAGGCCATCGATGTTTGCTATTATTATAGCCGCCTCCTC ATGTTCTGCATGAATGTTATCCCCAGTAGGCCGTCGATGTTTGCTATTATTATAGCCGCCTCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:31059203..31059298 26863196 MeRIP-seq:(Medium) rs765240471 Functional Loss SNV dbSNP153 33..33 33 - - - 88091 RMVar_ID_88091 Human_SNP_ID_8187172 m1A Human chr1 - 31059253 31059250 31059253 GGGAGGAGGAAGTGGAGGAGGCGGCTATAATAATAGCAAACATCGATGGCCTACTGGGGATAACA GGGAGGAGGAAGTGGAGGAGGCGGCTATAATA___GCAAACATCGATGGCCTACTGGGGATAACA CTAT C PUM1 Ensembl:ENSG00000134644 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:31007081..31059327;chr1:31007081..31059300 26863196 MeRIP-seq:(Medium) rs1378499024 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1745213,Human_RBP_ID_2142794,Human_RBP_ID_3309718,Human_RBP_ID_3933136,Human_RBP_ID_4093894,Human_RBP_ID_5518753,Human_RBP_ID_9562932,Human_RBP_ID_10930842,Human_RBP_ID_17748457,Human_RBP_ID_18430141,Human_RBP_ID_18967797,Human_RBP_ID_22874839,Human_RBP_ID_24763952,Human_RBP_ID_26310720,Human_RBP_ID_26861953,Human_RBP_ID_27797707 Human_Splice_Rec_39917,Human_Splice_Rec_39951,Human_Splice_Rec_39993,Human_Splice_Rec_40035,Human_Splice_Rec_40075,Human_Splice_Rec_40149,Human_Splice_Rec_40191,Human_Splice_Rec_40233,Human_Splice_Rec_40359,Human_Splice_Rec_40371 Human_miRNA_ID_1976370,Human_miRNA_ID_1976371 RMVar_hsa_circ_83915,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_131001,RMVar_hsa_circ_53855,RMVar_hsa_circ_82449,RMVar_hsa_circ_118532,RMVar_hsa_circ_131026,RMVar_hsa_circ_131027,RMVar_hsa_circ_116734,RMVar_hsa_circ_355888,RMVar_hsa_circ_131034,RMVar_hsa_circ_131035,RMVar_hsa_circ_64820,RMVar_hsa_circ_329239,RMVar_hsa_circ_131040,RMVar_hsa_circ_41241,RMVar_hsa_circ_298085,RMVar_hsa_circ_131042,RMVar_hsa_circ_131041,RMVar_hsa_circ_271456,RMVar_hsa_circ_131043,RMVar_hsa_circ_271730 88092 RMVar_ID_88092 Human_SNP_ID_8188978 m1A Human chr1 - 31065663 31065663 31065663 GTGAAAGGTAAGGGGGAGCGAGAGCGCCAGAGAGAGAAGATCGGGGGGCTGAAATCCATCTTCAT GTGAAAGGTAAGGGGGAGCGAGAGCGCCAGAGGGAGAAGATCGGGGGGCTGAAATCCATCTTCAT T C PUM1 Ensembl:ENSG00000134644 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31065542..31065725 26863196 MeRIP-seq:(Medium) rs1329486629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221972,Human_RBP_ID_741150,Human_RBP_ID_854252,Human_RBP_ID_1428980,Human_RBP_ID_3935651,Human_RBP_ID_4093902,Human_RBP_ID_5457507,Human_RBP_ID_5809312,Human_RBP_ID_10931015,Human_RBP_ID_18414916,Human_RBP_ID_26310722,Human_RBP_ID_27797713 Human_Splice_Rec_39915,Human_Splice_Rec_39949,Human_Splice_Rec_39991,Human_Splice_Rec_40073,Human_Splice_Rec_40147,Human_Splice_Rec_40337,Human_Splice_Rec_40345,Human_Splice_Rec_40357,Human_Splice_Rec_40369 Human_miRNA_ID_3115457 RMVar_hsa_circ_83915,RMVar_hsa_circ_130997,RMVar_hsa_circ_118532,RMVar_hsa_circ_131027,RMVar_hsa_circ_116734,RMVar_hsa_circ_131035 88093 RMVar_ID_88093 Human_SNP_ID_8188979 m1A Human chr1 - 31065667 31065667 31065667 CGGAGTGAAAGGTAAGGGGGAGCGAGAGCGCCAGAGAGAGAAGATCGGGGGGCTGAAATCCATCT CGGAGTGAAAGGTAAGGGGGAGCGAGAGCGCCGGAGAGAGAAGATCGGGGGGCTGAAATCCATCT T C PUM1 Ensembl:ENSG00000134644 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:31065547..31065700 26863196 MeRIP-seq:(Medium) rs1009600574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221972,Human_RBP_ID_741150,Human_RBP_ID_854252,Human_RBP_ID_3935651,Human_RBP_ID_4093902,Human_RBP_ID_5809312,Human_RBP_ID_10931015,Human_RBP_ID_18414916,Human_RBP_ID_26310722,Human_RBP_ID_27797713 Human_Splice_Rec_39915,Human_Splice_Rec_39949,Human_Splice_Rec_39991,Human_Splice_Rec_40073,Human_Splice_Rec_40147,Human_Splice_Rec_40337,Human_Splice_Rec_40345,Human_Splice_Rec_40357,Human_Splice_Rec_40369 Human_miRNA_ID_3115457 RMVar_hsa_circ_83915,RMVar_hsa_circ_130997,RMVar_hsa_circ_118532,RMVar_hsa_circ_131027,RMVar_hsa_circ_116734,RMVar_hsa_circ_131035 88094 RMVar_ID_88094 Human_SNP_ID_8213552 m1A Human chr1 - 31155123 31155123 31155123 CACCTCCGGCCCCGCGCCCGCGCCCGCGCCCGATCCTTCACGGACTCGTTCCGAAGATCCAGCCT CACCTCCGGCCCCGCGCCCGCGCCCGCGCCCGCTCCTTCACGGACTCGTTCCGAAGATCCAGCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:31155093..31155234;chr1:31155078..31155158 26863196 MeRIP-seq:(Medium) rs1557640438 Functional Loss SNV dbSNP153 33..33 33 - - - 88095 RMVar_ID_88095 Human_SNP_ID_8213795 m1A Human chr1 + 31155773 31155773 31155773 GTTGAGAGAATGGAAGTGAAGAGGAAGGCTTCACCATCACCTTAACTAACATGTGTTTCCTACCG GTTGAGAGAATGGAAGTGAAGAGGAAGGCTTCCCCATCACCTTAACTAACATGTGTTTCCTACCG A C lnc-ZCCHC17-17,lnc-ZCCHC17-17:2,lnc-ZCCHC17-17:3 RNACentral:URS0000D5BDAE,RNACentral:URS0000D58353,RNACentral:URS0000D58C10 lincRNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:31155677..31155793;chr1:31155702..31155795 26863196 MeRIP-seq:(Medium) rs111419304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17748468,Human_RBP_ID_23386976 88096 RMVar_ID_88096 Human_SNP_ID_8213797 m1A Human chr1 + 31155788 31155787 31155788 GTGAAGAGGAAGGCTTCACCATCACCTTAACTAACATGTGTTTCCTACCGTTAAATAAACATTAT GTGAAGAGGAAGGCTTCACCATCACCTTAACT_ACATGTGTTTCCTACCGTTAAATAAACATTAT TA T lnc-ZCCHC17-17,lnc-ZCCHC17-17:2,lnc-ZCCHC17-17:3 RNACentral:URS0000D5BDAE,RNACentral:URS0000D58353,RNACentral:URS0000D58C10 lincRNA,lincRNA,lincRNA intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:31155737..31155857 32194978 MeRIP-seq:(Medium) rs1427483103 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17748468 88097 RMVar_ID_88097 Human_SNP_ID_8241300 m1A Human chr1 - 31259933 31259933 31259933 ATTGCTAGCAAGAAACAGGAGGCGGTGGCCATATTCCAAAAACCACTTCTGTCCCATTTCACCAG ATTGCTAGCAAGAAACAGGAGGCGGTGGCCATGTTCCAAAAACCACTTCTGTCCCATTTCACCAG T C SNRNP40 Ensembl:ENSG00000060688 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31259884..31260060 26863196 MeRIP-seq:(Medium) rs188297244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351861,Human_RBP_ID_977534,Human_RBP_ID_5486102,Human_RBP_ID_5809362,Human_RBP_ID_9355891,Human_RBP_ID_17217872,Human_RBP_ID_17335205,Human_RBP_ID_17452303,Human_RBP_ID_17677550,Human_RBP_ID_17748484,Human_RBP_ID_26310723,Human_RBP_ID_27181206 Human_miRNA_ID_2057009 RMVar_hsa_circ_77241,RMVar_hsa_circ_131047 88098 RMVar_ID_88098 Human_SNP_ID_8247989 m1A Human chr1 - 31286422 31286422 31286422 GGTTAAGGAAGAGTCACACATGGCTTCAACCAAGAATGGGAATCACAATTCAAGTAGGGAAGGGT GGTTAAGGAAGAGTCACACATGGCTTCAACCAGGAATGGGAATCACAATTCAAGTAGGGAAGGGT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31286419..31286835 26863196 MeRIP-seq:(Medium) rs1426907408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_37953,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_346033,RMVar_hsa_circ_287591,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221 88099 RMVar_ID_88099 Human_SNP_ID_8249472 m1A Human chr1 + 31291981 31291979 31291981 CCACTGTGTCCCTTCAGTGTGGCATAGTTATCACAGTCACCATAGACATTCCACAGTACTGTTAG CCACTGTGTCCCTTCAGTGTGGCATAGTTAT__CAGTCACCATAGACATTCCACAGTACTGTTAG TCA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:31282474..31291987 32194978 MeRIP-seq:(Medium) rs1233331790 Functional Loss DEL dbSNP153 32..33 33 - - - 88100 RMVar_ID_88100 Human_SNP_ID_8250732 m1A Human chr1 - 31296671 31296671 31296671 GTCAAGCGGCAGCGGCATGAGTTGCTGTTGGGAGCGGGGTCTGGCCCAGGAGCCGGGCAGCAGCA GTCAAGCGGCAGCGGCATGAGTTGCTGTTGGGGGCGGGGTCTGGCCCAGGAGCCGGGCAGCAGCA T C SNRNP40 Ensembl:ENSG00000060688 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:31296601..31296750 32194978 MeRIP-seq:(Medium) rs1351432244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849769,Human_RBP_ID_4073798,Human_RBP_ID_5809590,Human_RBP_ID_9319881,Human_RBP_ID_9355893,Human_RBP_ID_18414917,Human_RBP_ID_18965132,Human_RBP_ID_22427053,Human_RBP_ID_23387091,Human_RBP_ID_26800195 Human_Splice_Rec_40407,Human_Splice_Rec_40449 RMVar_hsa_circ_131054,RMVar_hsa_circ_116377 88101 RMVar_ID_88101 Human_SNP_ID_8250778 m1A Human chr1 - 31296730 31296730 31296730 CGGTTGCCGCCATGATAGAACAGCAGAAGCGTAAGGGCCCAGAGTTGCCGCTGGTTCCAGTCAAG CGGTTGCCGCCATGATAGAACAGCAGAAGCGTGAGGGCCCAGAGTTGCCGCTGGTTCCAGTCAAG T C SNRNP40 Ensembl:ENSG00000060688 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:31293270..31296800 26863196 MeRIP-seq:(Medium) rs1404630171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272742,Human_RBP_ID_4044314,Human_RBP_ID_5311623,Human_RBP_ID_9319881,Human_RBP_ID_10932127,Human_RBP_ID_18414917,Human_RBP_ID_22427053 RMVar_hsa_circ_131054,RMVar_hsa_circ_116377 88102 RMVar_ID_88102 Human_SNP_ID_8250779 m1A Human chr1 + 31296731 31296731 31296731 TTGACTGGAACCAGCGGCAACTCTGGGCCCTTACGCTTCTGCTGTTCTATCATGGCGGCAACCGG TTGACTGGAACCAGCGGCAACTCTGGGCCCTTGCGCTTCTGCTGTTCTATCATGGCGGCAACCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:31296601..31296800;chr1:31293226..31296800 26863196 MeRIP-seq:(Medium) rs769245953 Functional Loss SNV dbSNP153 33..33 33 - - - 88103 RMVar_ID_88103 Human_SNP_ID_8250780 m1A Human chr1 + 31296731 31296731 31296731 TTGACTGGAACCAGCGGCAACTCTGGGCCCTTACGCTTCTGCTGTTCTATCATGGCGGCAACCGG TTGACTGGAACCAGCGGCAACTCTGGGCCCTTTCGCTTCTGCTGTTCTATCATGGCGGCAACCGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:31296601..31296800;chr1:31293226..31296800 26863196 MeRIP-seq:(Medium) rs769245953 Functional Loss SNV dbSNP153 33..33 33 - - - 88104 RMVar_ID_88104 Human_SNP_ID_8250786 m1A Human chr1 - 31296741 31296741 31296741 GCTGAAGAGACCGGTTGCCGCCATGATAGAACAGCAGAAGCGTAAGGGCCCAGAGTTGCCGCTGG GCTGAAGAGACCGGTTGCCGCCATGATAGAACTGCAGAAGCGTAAGGGCCCAGAGTTGCCGCTGG T A SNRNP40 Ensembl:ENSG00000060688 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31293301..31296800 26863196 MeRIP-seq:(Medium) rs1427002792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272742,Human_RBP_ID_4073798,Human_RBP_ID_10932127,Human_RBP_ID_18414917,Human_RBP_ID_22430365,Human_RBP_ID_23387093 RMVar_hsa_circ_131054,RMVar_hsa_circ_116377 88105 RMVar_ID_88105 Human_SNP_ID_8250940 m1A Human chr1 - 31297074 31297074 31297074 AGCCACCCACCCCGTTCTTCCTCATACGTACTAGGCGTCAGCTCCAGGTCCCCGAGTCGCTGCGC AGCCACCCACCCCGTTCTTCCTCATACGTACTGGGCGTCAGCTCCAGGTCCCCGAGTCGCTGCGC T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31297001..31310202 26863196 MeRIP-seq:(Medium) rs760519798 Functional Loss SNV dbSNP153 33..33 33 - - - 88106 RMVar_ID_88106 Human_SNP_ID_8253952 m1A Human chr1 - 31310094 31310094 31310094 CCATGGTCTCAGGCCTTCCTGAATTCATCCTTAATATTCTATGGCTCCTCCATTTCTCTTCTATT CCATGGTCTCAGGCCTTCCTGAATTCATCCTTGATATTCTATGGCTCCTCCATTTCTCTTCTATT T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31310011..31310099 26863196 MeRIP-seq:(Medium) rs1217888765 Functional Loss SNV dbSNP153 33..33 33 - - - 88107 RMVar_ID_88107 Human_SNP_ID_8266185 m1A Human chr1 - 31364091 31364090 31364092 GTGTGCCTTGCCCTCTTGCCTGTATCACTCTCAGAGTCTGAGCTGTCAGAGTCAGATGACTTCCT GTGTGCCTTGCCCTCTTGCCTGTATCACTCT__GAGTCTGAGCTGTCAGAGTCAGATGACTTCCT CTG C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31348949..31364283 26863196 MeRIP-seq:(Medium) rs748230256 Functional Loss DEL dbSNP153 32..33 33 - - - 88108 RMVar_ID_88108 Human_SNP_ID_8266341 m1A Human chr1 + 31364746 31364746 31364746 AACATAGTTCTACTATGCTAGAAGTGGCATCCAGCGGCCACAGCTAGAAAACAGTCTGCAGTGTG AACATAGTTCTACTATGCTAGAAGTGGCATCCTGCGGCCACAGCTAGAAAACAGTCTGCAGTGTG A T ZCCHC17 Ensembl:ENSG00000121766 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:31364726..31364750 32194978 MeRIP-seq:(Medium) rs1236462934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8308010,Human_RBP_ID_26387850 Human_miRNA_ID_170786,Human_miRNA_ID_1999221,Human_miRNA_ID_2669127 RMVar_hsa_circ_107566,RMVar_hsa_circ_131065 88109 RMVar_ID_88109 Human_SNP_ID_8277744 m1A Human chr1 - 31413279 31413252 31413279 GACTCACGCAGCTGAGCAGGGAGCAGGCTCCCAGGCAGGCCCCCATGGCGGCGGCTCCCGGCTTC GACTCACGCAGCTGAGCAGGGAGCAGGCTCCC___________________________GGCTTC CGGGAGCCGCCGCCATGGGGGCCTGCCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:31413277..31413408 26863196 MeRIP-seq:(Medium) rs1393026793 Functional Loss DEL dbSNP153 33..59 33 - - - 88110 RMVar_ID_88110 Human_SNP_ID_8277756 m1A Human chr1 - 31413267 31413267 31413267 TGAGCAGGGAGCAGGCTCCCAGGCAGGCCCCCATGGCGGCGGCTCCCGGCTTCGGGCGCCCGGCG TGAGCAGGGAGCAGGCTCCCAGGCAGGCCCCCGTGGCGGCGGCTCCCGGCTTCGGGCGCCCGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31413220..31413361 26863196 MeRIP-seq:(Medium) rs1227992077 Functional Loss SNV dbSNP153 33..33 33 - - - 88111 RMVar_ID_88111 Human_SNP_ID_8278004 m1A Human chr1 - 31414047 31414047 31414047 CGTGACGACCCGCACCCGCCTCACTCGAGGGCAGCTAAGAAAGTCCGGGGCTCCCTCCGCTCCCA CGTGACGACCCGCACCCGCCTCACTCGAGGGCGGCTAAGAAAGTCCGGGGCTCCCTCCGCTCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31414044..31414234 26863196 MeRIP-seq:(Medium) rs782722840 Functional Loss SNV dbSNP153 33..33 33 - - - 88112 RMVar_ID_88112 Human_SNP_ID_8280604 m1A Human chr1 - 31424761 31424761 31424761 CGTGGCGAAGCACATGCGGTAGACAGCGCGGTAGCCAAGCAGGGAGCCACAGTCGATGTGGCCCT CGTGGCGAAGCACATGCGGTAGACAGCGCGGTGGCCAAGCAGGGAGCCACAGTCGATGTGGCCCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:31423832..31425387 26863410 MeRIP-seq:(Medium) rs782371695 Functional Loss SNV dbSNP153 33..33 33 - - - 88113 RMVar_ID_88113 Human_SNP_ID_8281728 m1A Human chr1 + 31428600 31428600 31428600 GAGGCGCTGCCTGTGCGGAGATGCTGGGAAGGAACTTGTCAGAGGGAGGGCACAGCGACGGCAAA GAGGCGCTGCCTGTGCGGAGATGCTGGGAAGGCACTTGTCAGAGGGAGGGCACAGCGACGGCAAA A C SERINC2 Ensembl:ENSG00000168528 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31428572..31428856 26863196 MeRIP-seq:(Medium) rs1557496782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5301,RMVar_hsa_circ_104903,RMVar_hsa_circ_101940,RMVar_hsa_circ_131068,RMVar_hsa_circ_78468,RMVar_hsa_circ_116815,RMVar_hsa_circ_96339,RMVar_hsa_circ_131069,RMVar_hsa_circ_131070,RMVar_hsa_circ_131072,RMVar_hsa_circ_131076,RMVar_hsa_circ_328756,RMVar_hsa_circ_121489,RMVar_hsa_circ_131075,RMVar_hsa_circ_31310,RMVar_hsa_circ_125695,RMVar_hsa_circ_44032,RMVar_hsa_circ_131077,RMVar_hsa_circ_122052,RMVar_hsa_circ_117413,RMVar_hsa_circ_131078,RMVar_hsa_circ_131079,RMVar_hsa_circ_335345,RMVar_hsa_circ_43299,RMVar_hsa_circ_126817,RMVar_hsa_circ_131080,RMVar_hsa_circ_131081 88114 RMVar_ID_88114 Human_SNP_ID_8283313 m1A Human chr1 + 31432139 31432134 31432140 TGGATAGGGTGGTTAGGGTGGATAGGGTGGACAGGGTGGACAGGGTGGACAGGGTGGATAGGGTG TGGATAGGGTGGTTAGGGTGGATAGGGT______GGTGGACAGGGTGGACAGGGTGGATAGGGTG TGGACAG T SERINC2 Ensembl:ENSG00000168528 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31431921..31432200 26863196 MeRIP-seq:(Medium) rs1553134731 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_258952,Human_RBP_ID_800700,Human_RBP_ID_3330217,Human_RBP_ID_5156706,Human_RBP_ID_8166961,Human_RBP_ID_9410538,Human_RBP_ID_18928189,Human_RBP_ID_21961312,Human_RBP_ID_22350395,Human_RBP_ID_24550346,Human_RBP_ID_26774223 RMVar_hsa_circ_104903,RMVar_hsa_circ_101940,RMVar_hsa_circ_131068,RMVar_hsa_circ_78468,RMVar_hsa_circ_116815,RMVar_hsa_circ_96339,RMVar_hsa_circ_131069,RMVar_hsa_circ_131070,RMVar_hsa_circ_131072,RMVar_hsa_circ_131076,RMVar_hsa_circ_121489,RMVar_hsa_circ_131077,RMVar_hsa_circ_122052,RMVar_hsa_circ_117413,RMVar_hsa_circ_131079,RMVar_hsa_circ_43299,RMVar_hsa_circ_94979,RMVar_hsa_circ_126817,RMVar_hsa_circ_131080,RMVar_hsa_circ_131081,RMVar_hsa_circ_131083 88115 RMVar_ID_88115 Human_SNP_ID_8284380 m1A Human chr1 + 31434163 31434163 31434163 GCAGGGCTGCTCCTCTACCTGTGGACCCTGGTAGCCCCACTCCTCCTGCGCAACCGCGACTTCAG GCAGGGCTGCTCCTCTACCTGTGGACCCTGGTTGCCCCACTCCTCCTGCGCAACCGCGACTTCAG A T SERINC2 Ensembl:ENSG00000168528 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31434113..31434447 26863196 MeRIP-seq:(Medium) rs1553135336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23387284 Human_Splice_Rec_40620,Human_Splice_Rec_40638,Human_Splice_Rec_40664,Human_Splice_Rec_40684,Human_Splice_Rec_40702 RMVar_hsa_circ_104903,RMVar_hsa_circ_101940,RMVar_hsa_circ_131068,RMVar_hsa_circ_78468,RMVar_hsa_circ_116815,RMVar_hsa_circ_96339,RMVar_hsa_circ_131069,RMVar_hsa_circ_131070,RMVar_hsa_circ_131072,RMVar_hsa_circ_131076,RMVar_hsa_circ_121489,RMVar_hsa_circ_131077,RMVar_hsa_circ_122052,RMVar_hsa_circ_117413,RMVar_hsa_circ_131079,RMVar_hsa_circ_94979,RMVar_hsa_circ_126817,RMVar_hsa_circ_131080,RMVar_hsa_circ_131081,RMVar_hsa_circ_76026,RMVar_hsa_circ_131083,RMVar_hsa_circ_103128,RMVar_hsa_circ_131084,RMVar_hsa_circ_131085 88116 RMVar_ID_88116 Human_SNP_ID_8319467 m1A Human chr1 - 31576588 31576588 31576588 CCTCTGAGCAGGGGAGCGTCCCTACCTGGTGAAGGTGTGGGCTGGGGCCCAGGCTGGCCCGCGCG CCTCTGAGCAGGGGAGCGTCCCTACCTGGTGAGGGTGTGGGCTGGGGCCCAGGCTGGCCCGCGCG T C AC114488.1 Ensembl:ENSG00000229167 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:31576544..31576829 26863196 MeRIP-seq:(Medium) rs964682328 Functional Loss SNV dbSNP153 33..33 33 - - - 88117 RMVar_ID_88117 Human_SNP_ID_8319697 m1A Human chr1 + 31577327 31577324 31577327 GGAGCAGGACCTGTGCTGCCGCGGCCGTGCCGACGACTGTGCCCTGCCCTACCTGGGCGCCATCT GGAGCAGGACCTGTGCTGCCGCGGCCGTGC___CGACTGTGCCCTGCCCTACCTGGGCGCCATCT CCGA C TINAGL1,LINC01226 Ensembl:ENSG00000142910,Ensembl:ENSG00000284543 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31577276..31577397 26863196 MeRIP-seq:(Medium) rs1192018462 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4075365 RMVar_hsa_circ_82606,RMVar_hsa_circ_131087 88118 RMVar_ID_88118 Human_SNP_ID_8319701 m1A Human chr1 + 31577327 31577327 31577327 GGAGCAGGACCTGTGCTGCCGCGGCCGTGCCGACGACTGTGCCCTGCCCTACCTGGGCGCCATCT GGAGCAGGACCTGTGCTGCCGCGGCCGTGCCGCCGACTGTGCCCTGCCCTACCTGGGCGCCATCT A C TINAGL1,LINC01226 Ensembl:ENSG00000142910,Ensembl:ENSG00000284543 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31577276..31577397 26863196 MeRIP-seq:(Medium) rs1172830472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075365 RMVar_hsa_circ_82606,RMVar_hsa_circ_131087 88119 RMVar_ID_88119 Human_SNP_ID_8319735 m1A Human chr1 - 31577426 31577426 31577426 CTTGGATCGGGGGAAAAGGGGGTGGCACGCCGAGGCAGAAGTCCCAGAAGTCAGGGCAGCAGTCG CTTGGATCGGGGGAAAAGGGGGTGGCACGCCGTGGCAGAAGTCCCAGAAGTCAGGGCAGCAGTCG T A AC114488.1 Ensembl:ENSG00000229167 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31576526..31577475 26863196 MeRIP-seq:(Medium) rs148120255 Functional Loss SNV dbSNP153 33..33 33 - - - 88120 RMVar_ID_88120 Human_SNP_ID_8322749 m1A Human chr1 - 31586951 31586951 31586951 AGCCTCAGTGATGACCCATGTCCTCCATGCCCACGCGGCCCCAGACGCCCAGCACGAAGCTCTCG AGCCTCAGTGATGACCCATGTCCTCCATGCCCCCGCGGCCCCAGACGCCCAGCACGAAGCTCTCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31586852..31586954 26863196 MeRIP-seq:(Medium) rs774745359 Functional Loss SNV dbSNP153 33..33 33 - - - 88121 RMVar_ID_88121 Human_SNP_ID_8334690 m1A Human chr1 - 31632577 31632577 31632577 ATCGATGTCTACGGCTTCTCAGCCCTGTGGAAATTCATCCAGCAGTGGAAGAACCTCTTCCAGCA ATCGATGTCTACGGCTTCTCAGCCCTGTGGAATTTCATCCAGCAGTGGAAGAACCTCTTCCAGCA T A PEF1 Ensembl:ENSG00000162517 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:31632526..31632625 32194978 MeRIP-seq:(Medium) rs772440392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351975 Human_Splice_Rec_40984,Human_Splice_Rec_40985,Human_Splice_Rec_40990,Human_Splice_Rec_40991,Human_Splice_Rec_40996,Human_Splice_Rec_40997,Human_Splice_Rec_41004,Human_Splice_Rec_41005 Human_miRNA_ID_1999226,Human_miRNA_ID_1999227 RMVar_hsa_circ_49673,RMVar_hsa_circ_125900,RMVar_hsa_circ_131098,RMVar_hsa_circ_83660,RMVar_hsa_circ_131097 88122 RMVar_ID_88122 Human_SNP_ID_8335414 m1A Human chr1 + 31635355 31635355 31635355 CCAGAGGGGAACATCCCAGGATTGGGGTGTCCATAGGGCCCTCCACCAGCTGGTGGTCCATAAGG CCAGAGGGGAACATCCCAGGATTGGGGTGTCCCTAGGGCCCTCCACCAGCTGGTGGTCCATAAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31635304..31635513 26863196 MeRIP-seq:(Medium) rs1402785884 Functional Loss SNV dbSNP153 33..33 33 - - - 88123 RMVar_ID_88123 Human_SNP_ID_8335415 m1A Human chr1 + 31635355 31635355 31635355 CCAGAGGGGAACATCCCAGGATTGGGGTGTCCATAGGGCCCTCCACCAGCTGGTGGTCCATAAGG CCAGAGGGGAACATCCCAGGATTGGGGTGTCCGTAGGGCCCTCCACCAGCTGGTGGTCCATAAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31635304..31635513 26863196 MeRIP-seq:(Medium) rs1402785884 Functional Loss SNV dbSNP153 33..33 33 - - - 88124 RMVar_ID_88124 Human_SNP_ID_8335416 m1A Human chr1 - 31635356 31635356 31635356 GCCTTATGGACCACCAGCTGGTGGAGGGCCCTATGGACACCCCAATCCTGGGATGTTCCCCTCTG GCCTTATGGACCACCAGCTGGTGGAGGGCCCTGTGGACACCCCAATCCTGGGATGTTCCCCTCTG T C PEF1 Ensembl:ENSG00000162517 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:31635311..31635459 26863196 MeRIP-seq:(Medium) rs756072857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351980,Human_RBP_ID_977561,Human_RBP_ID_4044470,Human_RBP_ID_5234308,Human_RBP_ID_22429186 Human_miRNA_ID_2008339 RMVar_hsa_circ_131098,RMVar_hsa_circ_83660,RMVar_hsa_circ_266463 88125 RMVar_ID_88125 Human_SNP_ID_8339763 m1A Human chr1 + 31653958 31653958 31653958 GACCCTGGAGCACCTGGCCTGCCCGGAGCACCATCCTTCCCTGGAGGCCCTGGTCGTCCCGGAGC GACCCTGGAGCACCTGGCCTGCCCGGAGCACCTTCCTTCCCTGGAGGCCCTGGTCGTCCCGGAGC A T PEF1-AS1 Ensembl:ENSG00000235790 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31653910..31654042 26863196 MeRIP-seq:(Medium) rs764511890 Functional Loss SNV dbSNP153 33..33 33 - - - 88126 RMVar_ID_88126 Human_SNP_ID_8340203 m1A Human chr1 - 31655434 31655434 31655434 GGAGAGAAGGGGAGAGCCGGCATGCCTGGTGGACCTGGCAAGAGTGGTTCCATGGGGCCTGTTGG GGAGAGAAGGGGAGAGCCGGCATGCCTGGTGGCCCTGGCAAGAGTGGTTCCATGGGGCCTGTTGG T G COL16A1 Ensembl:ENSG00000084636 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31655384..31655511 26863196 MeRIP-seq:(Medium) rs1023408400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854270,Human_RBP_ID_18967822 Human_Splice_Rec_41314,Human_Splice_Rec_41358,Human_Splice_Rec_41386 88127 RMVar_ID_88127 Human_SNP_ID_8340917 m1A Human chr1 + 31658536 31658536 31658536 CCAGGGGGGCCGGGCTGGCCTGGGAGGCCTGCAAGGCCCCTTTCTCCGGTGGCTCCTCGGTCTCC CCAGGGGGGCCGGGCTGGCCTGGGAGGCCTGCTAGGCCCCTTTCTCCGGTGGCTCCTCGGTCTCC A T PEF1-AS1 Ensembl:ENSG00000235790 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31658452..31658560 26863196 MeRIP-seq:(Medium) rs566475071 Functional Loss SNV dbSNP153 33..33 33 - - - 88128 RMVar_ID_88128 Human_SNP_ID_8343067 m1A Human chr1 + 31666454 31666454 31666454 CTGGTCTTTGAGGCAGCCTGTGATCTGGCACCAGCCACCCCTTCCCACTTCTCCTCCCTCTCTCC CTGGTCTTTGAGGCAGCCTGTGATCTGGCACCCGCCACCCCTTCCCACTTCTCCTCCCTCTCTCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31666404..31666605 26863196 MeRIP-seq:(Medium) rs968141534 Functional Loss SNV dbSNP153 33..33 33 - - - 88129 RMVar_ID_88129 Human_SNP_ID_8343298 m1A Human chr1 - 31667527 31667527 31667527 GTGGGGCTGGATGCAGGGCTGCACGTGGAGCCACACAGTCTCGGGCTGGAGACTTGGCAGCAGCC GTGGGGCTGGATGCAGGGCTGCACGTGGAGCCCCACAGTCTCGGGCTGGAGACTTGGCAGCAGCC T G COL16A1 Ensembl:ENSG00000084636 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:31667525..31667628 26863196 MeRIP-seq:(Medium) rs751085893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76352,RMVar_hsa_circ_92412,RMVar_hsa_circ_131099,RMVar_hsa_circ_131100 88130 RMVar_ID_88130 Human_SNP_ID_8359034 m1A Human chr1 - 31727604 31727604 31727604 ATCTCCACGGCCCCTCCCGCTCCCTCCACAGGATAAGCCCAGCCCTGGGGAGCGCCCCAGCTTGT ATCTCCACGGCCCCTCCCGCTCCCTCCACAGGGTAAGCCCAGCCCTGGGGAGCGCCCCAGCTTGT T C ADGRB2 Ensembl:ENSG00000121753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:31727514..31727714 32194978 MeRIP-seq:(Medium) rs759490277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24683872 Human_Splice_Rec_41746,Human_Splice_Rec_41800,Human_Splice_Rec_41862,Human_Splice_Rec_41914,Human_Splice_Rec_41994,Human_Splice_Rec_42010,Human_Splice_Rec_42066,Human_Splice_Rec_42120 88131 RMVar_ID_88131 Human_SNP_ID_8360129 m1A Human chr1 - 31731370 31731370 31731370 AACACTTGCAACCCGTCCACCATCACGGGCACACTATCCCGCCTGTCCCTGGATGAGGATGAGGA AACACTTGCAACCCGTCCACCATCACGGGCACGCTATCCCGCCTGTCCCTGGATGAGGATGAGGA T C ADGRB2 Ensembl:ENSG00000121753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:31731240..31731390 32194978 MeRIP-seq:(Medium) rs756149100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_41738,Human_Splice_Rec_41794,Human_Splice_Rec_41854,Human_Splice_Rec_41908,Human_Splice_Rec_41926,Human_Splice_Rec_41986,Human_Splice_Rec_42002,Human_Splice_Rec_42058,Human_Splice_Rec_42114 RMVar_hsa_circ_131112,RMVar_hsa_circ_95942,RMVar_hsa_circ_90613,RMVar_hsa_circ_131113 88132 RMVar_ID_88132 Human_SNP_ID_8362447 m1A Human chr1 + 31739366 31739366 31739366 GGTGCGGTAGAGTACAGCACCGATCACAAAGTAGGAGGACTCATCAGGGTCTGCTGGGAGGAGGC GGTGCGGTAGAGTACAGCACCGATCACAAAGTGGGAGGACTCATCAGGGTCTGCTGGGAGGAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31739290..31739371 26863196 MeRIP-seq:(Medium) rs758262732 Functional Loss SNV dbSNP153 33..33 33 - - - 88133 RMVar_ID_88133 Human_SNP_ID_8362448 m1A Human chr1 + 31739366 31739366 31739366 GGTGCGGTAGAGTACAGCACCGATCACAAAGTAGGAGGACTCATCAGGGTCTGCTGGGAGGAGGC GGTGCGGTAGAGTACAGCACCGATCACAAAGTTGGAGGACTCATCAGGGTCTGCTGGGAGGAGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31739290..31739371 26863196 MeRIP-seq:(Medium) rs758262732 Functional Loss SNV dbSNP153 33..33 33 - - - 88134 RMVar_ID_88134 Human_SNP_ID_8364767 m1A Human chr1 + 31747333 31747333 31747333 ATTAACCCCCTCTGAACCAATGCTCCCAAATCATCATCCCCAGGCCCTGCCTCTCCTGTGCTCCA ATTAACCCCCTCTGAACCAATGCTCCCAAATCTTCATCCCCAGGCCCTGCCTCTCCTGTGCTCCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31747324..31747471 26863196 MeRIP-seq:(Medium) rs1191751794 Functional Loss SNV dbSNP153 33..33 33 - - - 88135 RMVar_ID_88135 Human_SNP_ID_8377010 m1A Human chr1 - 31798605 31798587 31798605 GGGCTCAGTGCCCCCGCCCTGCCCTGGCCTCCACAGCCTTCGGGAGCTCCCAGACCCAGTGCTGA GGGCTCAGTGCCCCCGCCCTGCCCTGGCCTCC__________________CAGACCCAGTGCTGA GGGAGCTCCCGAAGGCTGT G SPOCD1 Ensembl:ENSG00000134668 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31798603..31798710 26863196 MeRIP-seq:(Medium) rs767146196 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_83717,RMVar_hsa_circ_88514,RMVar_hsa_circ_131127,RMVar_hsa_circ_131128 88136 RMVar_ID_88136 Human_SNP_ID_8377020 m1A Human chr1 - 31798605 31798605 31798605 GGGCTCAGTGCCCCCGCCCTGCCCTGGCCTCCACAGCCTTCGGGAGCTCCCAGACCCAGTGCTGA GGGCTCAGTGCCCCCGCCCTGCCCTGGCCTCCGCAGCCTTCGGGAGCTCCCAGACCCAGTGCTGA T C SPOCD1 Ensembl:ENSG00000134668 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:31798603..31798710 26863196 MeRIP-seq:(Medium) rs780646311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83717,RMVar_hsa_circ_88514,RMVar_hsa_circ_131127,RMVar_hsa_circ_131128 88137 RMVar_ID_88137 Human_SNP_ID_8411721 m1A Human chr1 - 31937466 31937466 31937466 AGGAGTGTGGTAGGGTGTGCCGGCGTGTGTCCAGTGTGTGAGCAGGCATCCTAGAGGCCCTTCCC AGGAGTGTGGTAGGGTGTGCCGGCGTGTGTCCGGTGTGTGAGCAGGCATCCTAGAGGCCCTTCCC T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:31937417..31937568 26863196 MeRIP-seq:(Medium) rs560875390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1073126,Human_RBP_ID_3328328,Human_RBP_ID_5312430,Human_RBP_ID_5641601,Human_RBP_ID_8051734,Human_RBP_ID_8166963,Human_RBP_ID_9410541,Human_RBP_ID_17221027,Human_RBP_ID_19043084,Human_RBP_ID_21962316,Human_RBP_ID_22470333,Human_RBP_ID_22520234,Human_RBP_ID_23387710,Human_RBP_ID_26773042 RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 88138 RMVar_ID_88138 Human_SNP_ID_8411912 m1A Human chr1 + 31938084 31938069 31938084 TCAGTCACCTCGGCGGCGGCGGCGGCGGCGGTAGCGGTGGCGGCGGCGGCGACGACTCCCCCCCA TCAGTCACCTCGGCGGCG_______________GCGGTGGCGGCGGCGGCGACGACTCCCCCCCA GGCGGCGGCGGCGGTA G lnc-KHDRBS1-3 RNACentral:URS0000D5DEB8 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:31937976..31938350 26863410 MeRIP-seq:(Medium) rs1479029192 Functional Loss DEL dbSNP153 19..33 33 - - - 88139 RMVar_ID_88139 Human_SNP_ID_8411913 m1A Human chr1 + 31938084 31938072 31938084 TCAGTCACCTCGGCGGCGGCGGCGGCGGCGGTAGCGGTGGCGGCGGCGGCGACGACTCCCCCCCA TCAGTCACCTCGGCGGCGGCG____________GCGGTGGCGGCGGCGGCGACGACTCCCCCCCA GGCGGCGGCGGTA G lnc-KHDRBS1-3 RNACentral:URS0000D5DEB8 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:31937976..31938350 26863410 MeRIP-seq:(Medium) rs1193904403 Functional Loss DEL dbSNP153 22..33 33 - - - 88140 RMVar_ID_88140 Human_SNP_ID_8411919 m1A Human chr1 + 31938084 31938084 31938084 TCAGTCACCTCGGCGGCGGCGGCGGCGGCGGTAGCGGTGGCGGCGGCGGCGACGACTCCCCCCCA TCAGTCACCTCGGCGGCGGCGGCGGCGGCGGTGGCGGTGGCGGCGGCGGCGACGACTCCCCCCCA A G lnc-KHDRBS1-3 RNACentral:URS0000D5DEB8 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:31937976..31938350 26863410 MeRIP-seq:(Medium) rs533939255 Functional Loss SNV dbSNP153 33..33 33 - - - 88141 RMVar_ID_88141 Human_SNP_ID_8411931 m1A Human chr1 + 31938103 31938103 31938103 CGGCGGCGGCGGTAGCGGTGGCGGCGGCGGCGACGACTCCCCCCCAGCCTCGGCGCGCGACACCC CGGCGGCGGCGGTAGCGGTGGCGGCGGCGGCGGCGACTCCCCCCCAGCCTCGGCGCGCGACACCC A G lnc-KHDRBS1-3 RNACentral:URS0000D5DEB8 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:31937972..31938350 26863196 MeRIP-seq:(Medium) rs1425775747 Functional Loss SNV dbSNP153 33..33 33 - - - 88142 RMVar_ID_88142 Human_SNP_ID_8411934 m1A Human chr1 - 31938108 31938108 31938108 GGGCCGGGTGTCGCGCGCCGAGGCTGGGGGGGAGTCGTCGCCGCCGCCGCCACCGCTACCGCCGC GGGCCGGGTGTCGCGCGCCGAGGCTGGGGGGGGGTCGTCGCCGCCGCCGCCACCGCTACCGCCGC T C PTP4A2 Ensembl:ENSG00000184007 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:31938060..31938350 26863196 MeRIP-seq:(Medium) rs1183293117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222990,Human_RBP_ID_744251,Human_RBP_ID_804215,Human_RBP_ID_4072671,Human_RBP_ID_5810501,Human_RBP_ID_8968871,Human_RBP_ID_9318795,Human_RBP_ID_22531935,Human_RBP_ID_27555309 RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 88143 RMVar_ID_88143 Human_SNP_ID_8430581 m1A Human chr1 - 32013318 32013318 32013318 GGAGAAAGGAAGGCTGAGGGAGAGTCTGATGCAGGGGGAAAGTTGGGGAAGGGAAACCTGGAGGG GGAGAAAGGAAGGCTGAGGGAGAGTCTGATGCGGGGGGAAAGTTGGGGAAGGGAAACCTGGAGGG T C lnc-PTP4A2-6 RNACentral:URS0000D5E0AC lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32013269..32013394 26863196 MeRIP-seq:(Medium) rs544209342 Functional Loss SNV dbSNP153 33..33 33 - - - 88144 RMVar_ID_88144 Human_SNP_ID_8430853 m1A Human chr1 - 32013914 32013900 32013914 GAGGCCCGAGCGGCGGTTGGCGGGGGTGGCAGAGCGGGAGCGGTAGCGACCGAAGCCGACCCGAG GAGGCCCGAGCGGCGGTTGGCGGGGGTGGCAG______________CGACCGAAGCCGACCCGAG GCTACCGCTCCCGCT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:32013851..32014325 26863196 MeRIP-seq:(Medium) rs1451766524 Functional Loss DEL dbSNP153 33..46 33 - - - 88145 RMVar_ID_88145 Human_SNP_ID_8430876 m1A Human chr1 + 32013930 32013930 32013930 TCGCTACCGCTCCCGCTCTGCCACCCCCGCCAACCGCCGCTCGGGCCTCCGTCGCTGCCGCGTCG TCGCTACCGCTCCCGCTCTGCCACCCCCGCCACCCGCCGCTCGGGCCTCCGTCGCTGCCGCGTCG A C KHDRBS1 Ensembl:ENSG00000121774 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32013851..32014051 26863196 MeRIP-seq:(Medium) rs76080682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223421,Human_RBP_ID_352152,Human_RBP_ID_744865,Human_RBP_ID_4044702,Human_RBP_ID_5413923,Human_RBP_ID_5434015,Human_RBP_ID_5457524,Human_RBP_ID_5486124,Human_RBP_ID_18571930,Human_RBP_ID_22531937,Human_RBP_ID_26862118,Human_RBP_ID_27397579 88146 RMVar_ID_88146 Human_SNP_ID_8430877 m1A Human chr1 + 32013930 32013930 32013930 TCGCTACCGCTCCCGCTCTGCCACCCCCGCCAACCGCCGCTCGGGCCTCCGTCGCTGCCGCGTCG TCGCTACCGCTCCCGCTCTGCCACCCCCGCCAGCCGCCGCTCGGGCCTCCGTCGCTGCCGCGTCG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32013851..32014051 26863196 MeRIP-seq:(Medium) rs76080682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223421,Human_RBP_ID_352152,Human_RBP_ID_744865,Human_RBP_ID_4044702,Human_RBP_ID_5413923,Human_RBP_ID_5434015,Human_RBP_ID_5457524,Human_RBP_ID_5486124,Human_RBP_ID_18571930,Human_RBP_ID_22531937,Human_RBP_ID_26862118,Human_RBP_ID_27397579 88147 RMVar_ID_88147 Human_SNP_ID_8431008 m1A Human chr1 - 32014228 32014228 32014228 GGGGCAGCAGCGGGGTCGGCGCTGGCCCGCCCACTGTCGCGTCGGGACCCGTGGCCGAGGGCGGC GGGGCAGCAGCGGGGTCGGCGCTGGCCCGCCCGCTGTCGCGTCGGGACCCGTGGCCGAGGGCGGC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:32014127..32014283 26863410 MeRIP-seq:(Medium) rs528464512 Functional Loss SNV dbSNP153 33..33 33 - - - 88148 RMVar_ID_88148 Human_SNP_ID_8431024 m1A Human chr1 - 32014252 32014252 32014252 TCTTGACCGAGGCTGTGGCCGAGGGGGGCAGCAGCGGGGTCGGCGCTGGCCCGCCCACTGTCGCG TCTTGACCGAGGCTGTGGCCGAGGGGGGCAGCGGCGGGGTCGGCGCTGGCCCGCCCACTGTCGCG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:32014168..32014260 26863410 MeRIP-seq:(Medium) rs867892253 Functional Loss SNV dbSNP153 33..33 33 - - - 88149 RMVar_ID_88149 Human_SNP_ID_8437650 m1A Human chr1 + 32037883 32037883 32037883 CCACCTCGGGGGGCTTTGGTACGTGGTACACCAGTAAGGGGAGCCATCACCAGAGGTGCCACTGT CCACCTCGGGGGGCTTTGGTACGTGGTACACCGGTAAGGGGAGCCATCACCAGAGGTGCCACTGT A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:32037826..32038050 32194978 MeRIP-seq:(Medium) rs1400359432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851376,Human_RBP_ID_1745383,Human_RBP_ID_3933141,Human_RBP_ID_8308189,Human_RBP_ID_8754884,Human_RBP_ID_9270005,Human_RBP_ID_9355902,Human_RBP_ID_17748679,Human_RBP_ID_18571958,Human_RBP_ID_22429195,Human_RBP_ID_22749016,Human_RBP_ID_26378988 Human_Splice_Rec_42478,Human_Splice_Rec_42494,Human_Splice_Rec_42508,Human_Splice_Rec_42524 RMVar_hsa_circ_131144,RMVar_hsa_circ_300160,RMVar_hsa_circ_324915,RMVar_hsa_circ_341253,RMVar_hsa_circ_275865,RMVar_hsa_circ_131145,RMVar_hsa_circ_36591,RMVar_hsa_circ_104735,RMVar_hsa_circ_362480,RMVar_hsa_circ_277259,RMVar_hsa_circ_131147,RMVar_hsa_circ_131146,RMVar_hsa_circ_293622,RMVar_hsa_circ_317843,RMVar_hsa_circ_301169,RMVar_hsa_circ_272589,RMVar_hsa_circ_125672,RMVar_hsa_circ_131151,RMVar_hsa_circ_131152,RMVar_hsa_circ_131153,RMVar_hsa_circ_299756,RMVar_hsa_circ_279525,RMVar_hsa_circ_131154,RMVar_hsa_circ_131155,RMVar_hsa_circ_131156 88150 RMVar_ID_88150 Human_SNP_ID_8439029 m1A Human chr1 - 32043445 32043445 32043445 AAAGATTCTTCATGGCTAAAAAGCTCTGCATCAAACTCAATTCAGGAGGCCTTCCCTCCCCACCA AAAGATTCTTCATGGCTAAAAAGCTCTGCATCCAACTCAATTCAGGAGGCCTTCCCTCCCCACCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:32043301..32043575 32194978 MeRIP-seq:(Medium) rs1228297455 Functional Loss SNV dbSNP153 33..33 33 - - - 88151 RMVar_ID_88151 Human_SNP_ID_8446255 m1A Human chr1 + 32073007 32073007 32073007 CCGGCCGCCGTCGCCTCCGACATATTGCCCGCAGGAGCTGCGGCGGCGAAGCGGAGAGCACCGGG CCGGCCGCCGTCGCCTCCGACATATTGCCCGCCGGAGCTGCGGCGGCGAAGCGGAGAGCACCGGG A C TMEM39B Ensembl:ENSG00000121775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32072957..32073233;chr1:32072958..32073215;chr1:32072958..32073189 26863196 MeRIP-seq:(Medium) rs761440235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073803 Human_Splice_Rec_42555,Human_Splice_Rec_42563,Human_Splice_Rec_42579,Human_Splice_Rec_42591,Human_Splice_Rec_42601,Human_Splice_Rec_42619 88152 RMVar_ID_88152 Human_SNP_ID_8456109 m1A Human chr1 + 32108111 32108111 32108111 CTGAAGCTGCCGCCGTTGCCTCCGCCGCCAAGAGTGAGCGAGCGGACCCGCGATGGGTGAGTGAG CTGAAGCTGCCGCCGTTGCCTCCGCCGCCAAGCGTGAGCGAGCGGACCCGCGATGGGTGAGTGAG A C KPNA6 Ensembl:ENSG00000025800 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:32108051..32108191;chr1:32108051..32154725 26863196 MeRIP-seq:(Medium) rs201697054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741334,Human_RBP_ID_4073805,Human_RBP_ID_9270006,Human_RBP_ID_18414919 Human_Splice_Rec_42657,Human_Splice_Rec_42683 RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 88153 RMVar_ID_88153 Human_SNP_ID_8456111 m1A Human chr1 + 32108115 32108115 32108115 AGCTGCCGCCGTTGCCTCCGCCGCCAAGAGTGAGCGAGCGGACCCGCGATGGGTGAGTGAGGAAA AGCTGCCGCCGTTGCCTCCGCCGCCAAGAGTGCGCGAGCGGACCCGCGATGGGTGAGTGAGGAAA A C KPNA6 Ensembl:ENSG00000025800 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32108051..32108227 26863196 MeRIP-seq:(Medium) rs1310047646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741334,Human_RBP_ID_4073805,Human_RBP_ID_9270006,Human_RBP_ID_18414919 Human_Splice_Rec_42657,Human_Splice_Rec_42683 RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 88154 RMVar_ID_88154 Human_SNP_ID_8456112 m1A Human chr1 + 32108115 32108115 32108115 AGCTGCCGCCGTTGCCTCCGCCGCCAAGAGTGAGCGAGCGGACCCGCGATGGGTGAGTGAGGAAA AGCTGCCGCCGTTGCCTCCGCCGCCAAGAGTGTGCGAGCGGACCCGCGATGGGTGAGTGAGGAAA A T KPNA6 Ensembl:ENSG00000025800 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32108051..32108227 26863196 MeRIP-seq:(Medium) rs1310047646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741334,Human_RBP_ID_4073805,Human_RBP_ID_9270006,Human_RBP_ID_18414919 Human_Splice_Rec_42657,Human_Splice_Rec_42683 RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 88155 RMVar_ID_88155 Human_SNP_ID_8472595 m1A Human chr1 - 32169939 32169939 32169939 AGTCCATTGAGGGCCACTTGCACAATCTTCGAATCCATTACAGTCAGCAAGTCACATAGGGGTTT AGTCCATTGAGGGCCACTTGCACAATCTTCGAGTCCATTACAGTCAGCAAGTCACATAGGGGTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:32169888..32170734 32194978 MeRIP-seq:(Medium) rs777002762 Functional Loss SNV dbSNP153 33..33 33 - - - 88156 RMVar_ID_88156 Human_SNP_ID_8473023 m1A Human chr1 + 32171661 32171661 32171661 GGGGATCCTCCTCACTCTCCTGAAGTGTCTCAAGTATACCAGTGGGAGTGCAGGGGAGGAGCACA GGGGATCCTCCTCACTCTCCTGAAGTGTCTCACGTATACCAGTGGGAGTGCAGGGGAGGAGCACA A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs182809314 Functional Loss SNV dbSNP153 33..33 33 - - - 88157 RMVar_ID_88157 Human_SNP_ID_8473024 m1A Human chr1 + 32171661 32171661 32171661 GGGGATCCTCCTCACTCTCCTGAAGTGTCTCAAGTATACCAGTGGGAGTGCAGGGGAGGAGCACA GGGGATCCTCCTCACTCTCCTGAAGTGTCTCAGGTATACCAGTGGGAGTGCAGGGGAGGAGCACA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs182809314 Functional Loss SNV dbSNP153 33..33 33 - - - 88158 RMVar_ID_88158 Human_SNP_ID_8474074 m1A Human chr1 - 32175957 32175953 32175957 AGATCACAGGTGCCCACCACCACACCTGGCTTATTTTTTTTATTTTTTTATTTTTGTAGGGACGG AGATCACAGGTGCCCACCACCACACCTGGCTT____TTTTTATTTTTTTATTTTTGTAGGGACGG AAAAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32175911..32176038 26863196 MeRIP-seq:(Medium) rs1364916130 Functional Loss DEL dbSNP153 33..36 33 - - - 88159 RMVar_ID_88159 Human_SNP_ID_8475019 m1A Human chr1 - 32179773 32179773 32179773 TCTCGCCCACCGGCCGCCGCTGCACGTACCTCACCGCCGACGTCCGATGGCTTCCCCACCTCTGG TCTCGCCCACCGGCCGCCGCTGCACGTACCTCCCCGCCGACGTCCGATGGCTTCCCCACCTCTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32179701..32179870;chr1:32179676..32179892;chr1:32179701..32179855 26863196 MeRIP-seq:(Medium) rs372446853 Functional Loss SNV dbSNP153 33..33 33 - - - 88160 RMVar_ID_88160 Human_SNP_ID_8475143 m1A Human chr1 + 32180053 32180053 32180053 CCCTGAGCCAATCCCGCGCCCGGCCTGCCGCGAGGGGGCCGGTTGTGCCGGGAAGTGGCTCCAGG CCCTGAGCCAATCCCGCGCCCGGCCTGCCGCGTGGGGGCCGGTTGTGCCGGGAAGTGGCTCCAGG A T TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32180048..32180205 26863196 MeRIP-seq:(Medium) rs966676480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5311629,Human_RBP_ID_9318800 RMVar_hsa_circ_93633,RMVar_hsa_circ_110372,RMVar_hsa_circ_100949,RMVar_hsa_circ_131177,RMVar_hsa_circ_131178,RMVar_hsa_circ_131179 88161 RMVar_ID_88161 Human_SNP_ID_8475157 m1A Human chr1 + 32180090 32180090 32180090 GCCGGTTGTGCCGGGAAGTGGCTCCAGGGAGAAGAGGCCTCTTCCCTCACCCGCTGTGGGAGCTG GCCGGTTGTGCCGGGAAGTGGCTCCAGGGAGATGAGGCCTCTTCCCTCACCCGCTGTGGGAGCTG A T TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32180086..32180202 26863196 MeRIP-seq:(Medium) rs1369735124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93633,RMVar_hsa_circ_110372,RMVar_hsa_circ_100949,RMVar_hsa_circ_131177,RMVar_hsa_circ_131178,RMVar_hsa_circ_131179,RMVar_hsa_circ_131180,RMVar_hsa_circ_76653 88162 RMVar_ID_88162 Human_SNP_ID_8477004 m1A Human chr1 + 32186228 32186226 32186229 GAAATGAGTTGCTAGAGTGGTGTTGTGAGTAGAGGAGGGGAGCTGAGGCCTGCCCAAGAAGGGGG GAAATGAGTTGCTAGAGTGGTGTTGTGAGTA___GAGGGGAGCTGAGGCCTGCCCAAGAAGGGGG AGAG A TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32186222..32186409 26863196 MeRIP-seq:(Medium) rs1287674738 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5811354,Human_RBP_ID_10940608,Human_RBP_ID_17099223 RMVar_hsa_circ_24950,RMVar_hsa_circ_93633,RMVar_hsa_circ_110372,RMVar_hsa_circ_100949,RMVar_hsa_circ_110146,RMVar_hsa_circ_131177,RMVar_hsa_circ_131178,RMVar_hsa_circ_131179,RMVar_hsa_circ_131180,RMVar_hsa_circ_76653,RMVar_hsa_circ_104478,RMVar_hsa_circ_131183,RMVar_hsa_circ_39868,RMVar_hsa_circ_131181,RMVar_hsa_circ_131182,RMVar_hsa_circ_275247,RMVar_hsa_circ_301133,RMVar_hsa_circ_131184 88163 RMVar_ID_88163 Human_SNP_ID_8477079 m1A Human chr1 + 32186552 32186552 32186552 TGTAAAGCAGGAAGGTGCTTTACTAGGGTTGCAGTACTACTGGGGAAGGGCCAAGAGAGTTGAGG TGTAAAGCAGGAAGGTGCTTTACTAGGGTTGCGGTACTACTGGGGAAGGGCCAAGAGAGTTGAGG A G TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32186546..32186796 26863196 MeRIP-seq:(Medium) rs1197545574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17103192,Human_RBP_ID_22562784,Human_RBP_ID_22784330,Human_RBP_ID_23388095 RMVar_hsa_circ_24950,RMVar_hsa_circ_93633,RMVar_hsa_circ_110372,RMVar_hsa_circ_100949,RMVar_hsa_circ_110146,RMVar_hsa_circ_131177,RMVar_hsa_circ_131178,RMVar_hsa_circ_131179,RMVar_hsa_circ_131180,RMVar_hsa_circ_76653,RMVar_hsa_circ_104478,RMVar_hsa_circ_131183,RMVar_hsa_circ_39868,RMVar_hsa_circ_131181,RMVar_hsa_circ_131182,RMVar_hsa_circ_275247,RMVar_hsa_circ_301133,RMVar_hsa_circ_131184 88164 RMVar_ID_88164 Human_SNP_ID_8479217 m1A Human chr1 + 32194949 32194949 32194949 AAAGAACTGGAGGGCCTGCAGGTAAAAATCCAACGGCTGGAGAAGCTGTGCCGGGCACTGCAGAC AAAGAACTGGAGGGCCTGCAGGTAAAAATCCAGCGGCTGGAGAAGCTGTGCCGGGCACTGCAGAC A G TXLNA Ensembl:ENSG00000084652 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32194882..32194986 26863196 MeRIP-seq:(Medium) rs1443487517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1212,Human_RBP_ID_849785,Human_RBP_ID_1348144,Human_RBP_ID_3935668,Human_RBP_ID_5811412,Human_RBP_ID_9355925,Human_RBP_ID_10940910,Human_RBP_ID_17748822,Human_RBP_ID_18965159,Human_RBP_ID_27797733 Human_Splice_Rec_42762,Human_Splice_Rec_42780 Human_miRNA_ID_2972042,Human_miRNA_ID_3005225 RMVar_hsa_circ_110146,RMVar_hsa_circ_131182,RMVar_hsa_circ_89580,RMVar_hsa_circ_131188 88165 RMVar_ID_88165 Human_SNP_ID_8479295 m1A Human chr1 + 32195171 32195169 32195171 AGCACAGAAGCATCAGGCCAGACTGGGCCTCAAGAGCCCACCTCCGCCAGGGCCTAGAGAGCCTG AGCACAGAAGCATCAGGCCAGACTGGGCCTC__GAGCCCACCTCCGCCAGGGCCTAGAGAGCCTG CAA C lnc-TMEM234-4 RNACentral:URS00008C22EF lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1361369391 Functional Loss DEL dbSNP153 32..33 33 - - - 88166 RMVar_ID_88166 Human_SNP_ID_8480999 m1A Human chr1 - 32201881 32201881 32201881 CCTAGGAGGGAAGCAACCCCACAAAGATAGCCAGGGGCAAAGTTAGCCCTTCACCCAGAAATCCC CCTAGGAGGGAAGCAACCCCACAAAGATAGCCGGGGGCAAAGTTAGCCCTTCACCCAGAAATCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32201880..32202069 26863196 MeRIP-seq:(Medium) rs181133472 Functional Loss SNV dbSNP153 33..33 33 - - - 88167 RMVar_ID_88167 Human_SNP_ID_8481042 m1A Human chr1 + 32202026 32202018 32202026 CCCCAGGCACACTACGGAGGGTCCCTGTGCCTACCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CCCCAGGCACACTACGGAGGGTCCC________CCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CTGTGCCTA C CCDC28B Ensembl:ENSG00000160050 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32202001..32202025 26863196 MeRIP-seq:(Medium) rs1192282930 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_4045405,Human_RBP_ID_9318801 Human_Splice_Rec_42783,Human_Splice_Rec_42793,Human_Splice_Rec_42797,Human_Splice_Rec_42805,Human_Splice_Rec_42813 88168 RMVar_ID_88168 Human_SNP_ID_8481046 m1A Human chr1 + 32202026 32202024 32202026 CCCCAGGCACACTACGGAGGGTCCCTGTGCCTACCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CCCCAGGCACACTACGGAGGGTCCCTGTGCC__CCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CTA C CCDC28B Ensembl:ENSG00000160050 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32202001..32202025 26863196 MeRIP-seq:(Medium) rs1553138464 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4045405,Human_RBP_ID_9318801 Human_Splice_Rec_42783,Human_Splice_Rec_42793,Human_Splice_Rec_42797,Human_Splice_Rec_42805,Human_Splice_Rec_42813 88169 RMVar_ID_88169 Human_SNP_ID_8481047 m1A Human chr1 + 32202026 32202026 32202026 CCCCAGGCACACTACGGAGGGTCCCTGTGCCTACCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CCCCAGGCACACTACGGAGGGTCCCTGTGCCTCCCAGCCACAGCGGCTCCTTGGCCCTAGGACTT A C CCDC28B Ensembl:ENSG00000160050 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32202001..32202025 26863196 MeRIP-seq:(Medium) rs200013564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4045405,Human_RBP_ID_9318801 Human_Splice_Rec_42783,Human_Splice_Rec_42793,Human_Splice_Rec_42797,Human_Splice_Rec_42805,Human_Splice_Rec_42813 88170 RMVar_ID_88170 Human_SNP_ID_8481676 m1A Human chr1 + 32204285 32204285 32204285 CTTCAGCCTGGATGTGTGTGGGGAGGAGGAGGACGATGAAGAGGAAGAGGATGGGGTCACTGAGG CTTCAGCCTGGATGTGTGTGGGGAGGAGGAGGGCGATGAAGAGGAAGAGGATGGGGTCACTGAGG A G CCDC28B Ensembl:ENSG00000160050 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32204234..32204365 26863196 MeRIP-seq:(Medium) rs200566328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109060,Human_RBP_ID_5136175,Human_RBP_ID_5332996,Human_RBP_ID_18430158,Human_RBP_ID_21962900,Human_RBP_ID_22430382,Human_RBP_ID_26310750,Human_RBP_ID_27797735 Human_Splice_Rec_42786,Human_Splice_Rec_42787,Human_Splice_Rec_42800,Human_Splice_Rec_42801,Human_Splice_Rec_42808,Human_Splice_Rec_42809 88171 RMVar_ID_88171 Human_SNP_ID_8482178 m1A Human chr1 - 32205725 32205725 32205725 AAAAATCCTGTGAACCCCGCGCCCGCCCCCGCACCTGCAATGCAGACACCTTCCGAACCAGCAGC AAAAATCCTGTGAACCCCGCGCCCGCCCCCGCTCCTGCAATGCAGACACCTTCCGAACCAGCAGC T A AL049795.1 Ensembl:ENSG00000224066 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32205702..32205795 26863196 MeRIP-seq:(Medium) rs1557520941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8244239,Human_RBP_ID_10941247 Human_Splice_Rec_42826 88172 RMVar_ID_88172 Human_SNP_ID_8482406 m1A Human chr1 - 32206251 32206251 32206251 GCGGCCTGGGAATGCGGCCCTCGGTCCACTGAAGCGTGCCCAGGTCGCCCTCGACCTCTCGTACA GCGGCCTGGGAATGCGGCCCTCGGTCCACTGAGGCGTGCCCAGGTCGCCCTCGACCTCTCGTACA T C AL049795.1 Ensembl:ENSG00000224066 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32206200..32206295 26863196 MeRIP-seq:(Medium) rs1430251291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22871237,Human_RBP_ID_24745264 Human_Splice_Rec_42824 88173 RMVar_ID_88173 Human_SNP_ID_8482539 m1A Human chr1 + 32206645 32206645 32206645 CTGGGAGGAGATGGTGCTGAAGAAGTCAGGAGAGAGCTCAGCAAATCAAGGAAGCCTCTGCAGAG CTGGGAGGAGATGGTGCTGAAGAAGTCAGGAGGGAGCTCAGCAAATCAAGGAAGCCTCTGCAGAG A G IQCC Ensembl:ENSG00000160051 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32206594..32206701 26863196 MeRIP-seq:(Medium) rs1404215424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26313802 RMVar_hsa_circ_93886,RMVar_hsa_circ_131189 88174 RMVar_ID_88174 Human_SNP_ID_8487178 m1A Human chr1 + 32221940 32221940 32221940 GCTGGGCCCAGGTCGGCTCATGAACCCGCTGCAGGCCGGCGGAGGCCCGCTTCAGCAGCGGCTGC GCTGGGCCCAGGTCGGCTCATGAACCCGCTGCGGGCCGGCGGAGGCCCGCTTCAGCAGCGGCTGC A G EIF3I Ensembl:ENSG00000084623 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32221895..32222012 26863196 MeRIP-seq:(Medium) rs1207489028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_42987 RMVar_hsa_circ_119039,RMVar_hsa_circ_131194 88175 RMVar_ID_88175 Human_SNP_ID_8487461 m1A Human chr1 + 32222538 32222538 32222538 CGAGCACTGACGTTACTGTCTTGTCCCCACAGAAGCCGATCCTACTGCAGGGCCATGAGCGGTCC CGAGCACTGACGTTACTGTCTTGTCCCCACAGGAGCCGATCCTACTGCAGGGCCATGAGCGGTCC A G EIF3I Ensembl:ENSG00000084623 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1355560564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352437,Human_RBP_ID_851382,Human_RBP_ID_4073814,Human_RBP_ID_5331391,Human_RBP_ID_5413926,Human_RBP_ID_8308403,Human_RBP_ID_9318804,Human_RBP_ID_22633353,Human_RBP_ID_26773368,Human_RBP_ID_27397697 Human_Splice_Rec_42990,Human_Splice_Rec_42991,Human_Splice_Rec_42998,Human_Splice_Rec_42999,Human_Splice_Rec_43018,Human_Splice_Rec_43019,Human_Splice_Rec_43027,Human_Splice_Rec_43039,Human_Splice_Rec_43049 Human_miRNA_ID_2379857,Human_miRNA_ID_3022874 RMVar_hsa_circ_5429,RMVar_hsa_circ_113464,RMVar_hsa_circ_119039,RMVar_hsa_circ_117004,RMVar_hsa_circ_131194,RMVar_hsa_circ_103728,RMVar_hsa_circ_131196,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_131195,RMVar_hsa_circ_88535,RMVar_hsa_circ_131198,RMVar_hsa_circ_131199 88176 RMVar_ID_88176 Human_SNP_ID_8487464 m1A Human chr1 + 32222544 32222544 32222544 CTGACGTTACTGTCTTGTCCCCACAGAAGCCGATCCTACTGCAGGGCCATGAGCGGTCCATTACG CTGACGTTACTGTCTTGTCCCCACAGAAGCCGGTCCTACTGCAGGGCCATGAGCGGTCCATTACG A G EIF3I Ensembl:ENSG00000084623 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32222526..32222670 26863196 MeRIP-seq:(Medium) rs745439479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17798,Human_RBP_ID_352437,Human_RBP_ID_851382,Human_RBP_ID_1429309,Human_RBP_ID_4073815,Human_RBP_ID_5331391,Human_RBP_ID_5413926,Human_RBP_ID_8308403,Human_RBP_ID_9318804,Human_RBP_ID_17677600,Human_RBP_ID_22633353,Human_RBP_ID_22784385,Human_RBP_ID_26773368,Human_RBP_ID_26862445 Human_Splice_Rec_42990,Human_Splice_Rec_42991,Human_Splice_Rec_42998,Human_Splice_Rec_42999,Human_Splice_Rec_43018,Human_Splice_Rec_43019,Human_Splice_Rec_43027,Human_Splice_Rec_43039,Human_Splice_Rec_43049 Human_miRNA_ID_2379857,Human_miRNA_ID_2426118,Human_miRNA_ID_3022874 RMVar_hsa_circ_5429,RMVar_hsa_circ_113464,RMVar_hsa_circ_119039,RMVar_hsa_circ_117004,RMVar_hsa_circ_131194,RMVar_hsa_circ_103728,RMVar_hsa_circ_131196,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_131195,RMVar_hsa_circ_88535,RMVar_hsa_circ_131198,RMVar_hsa_circ_131199 88177 RMVar_ID_88177 Human_SNP_ID_8492296 m1A Human chr1 - 32241422 32241422 32241422 GGACCTGTGGCTGCTGCTGTTGCGTAGCGTCGACTCCTTCGAGAAGCAGTGAGACGTGGCGGGGT GGACCTGTGGCTGCTGCTGTTGCGTAGCGTCGCCTCCTTCGAGAAGCAGTGAGACGTGGCGGGGT T G MTMR9LP Ensembl:ENSG00000220785 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32241373..32241612 26863196 MeRIP-seq:(Medium) rs1266997764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5538566 88178 RMVar_ID_88178 Human_SNP_ID_8492552 m1A Human chr1 + 32242435 32242431 32242435 AAGAAGAAAGGAAGGAAGGAGGGAGGGAGGGAAGGAAGGAAGGAAGGAAAGAAAGAAGGAAGGAA AAGAAGAAAGGAAGGAAGGAGGGAGGGAG____GGAAGGAAGGAAGGAAAGAAAGAAGGAAGGAA GGGAA G lnc-FAM167B-1 RNACentral:URS00008BA389 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32242387..32242471 26863196 MeRIP-seq:(Medium) rs1216681396 Functional Loss DEL dbSNP153 30..33 33 - - - 88179 RMVar_ID_88179 Human_SNP_ID_8492555 m1A Human chr1 + 32242435 32242435 32242435 AAGAAGAAAGGAAGGAAGGAGGGAGGGAGGGAAGGAAGGAAGGAAGGAAAGAAAGAAGGAAGGAA AAGAAGAAAGGAAGGAAGGAGGGAGGGAGGGAGGGAAGGAAGGAAGGAAAGAAAGAAGGAAGGAA A G lnc-FAM167B-1 RNACentral:URS00008BA389 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32242387..32242471 26863196 MeRIP-seq:(Medium) rs542300811 Functional Loss SNV dbSNP153 33..33 33 - - - 88180 RMVar_ID_88180 Human_SNP_ID_8492586 m1A Human chr1 + 32242488 32242488 32242488 AGAAGGAAGGAAGGAAGGAAGGAAAGGAAGAAAGATAACTATCTCTTCCACCATACCCTGGTGGA AGAAGGAAGGAAGGAAGGAAGGAAAGGAAGAACGATAACTATCTCTTCCACCATACCCTGGTGGA A C lnc-FAM167B-1 RNACentral:URS00008BA389 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32242438..32242537 26863196 MeRIP-seq:(Medium) rs967746295 Functional Loss SNV dbSNP153 33..33 33 - - - 88181 RMVar_ID_88181 Human_SNP_ID_8514810 m1A Human chr1 + 32329818 32329816 32329819 GTGCTGATGTTTAAGCTGGACTTTGGAAAATGAGGAGGTGCCCATGTGAAGAAGGAGGTGATGGC GTGCTGATGTTTAAGCTGGACTTTGGAAAAT___GAGGTGCCCATGTGAAGAAGGAGGTGATGGC TGAG T HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32329768..32329937 26863196 MeRIP-seq:(Medium) rs1557612574 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10942159,Human_RBP_ID_22562788,Human_RBP_ID_23388302 RMVar_hsa_circ_116794,RMVar_hsa_circ_131229,RMVar_hsa_circ_110997,RMVar_hsa_circ_91934,RMVar_hsa_circ_131231,RMVar_hsa_circ_131233,RMVar_hsa_circ_81817,RMVar_hsa_circ_109004,RMVar_hsa_circ_131234,RMVar_hsa_circ_131235 88182 RMVar_ID_88182 Human_SNP_ID_8515429 m1A Human chr1 + 32332167 32332167 32332167 ATTCTGAAGAGGAGGGAGAGGGGGGCCGCAAGAACTCTTCCAACTTCAAAAAAGCCAAGAGAGTC ATTCTGAAGAGGAGGGAGAGGGGGGCCGCAAGCACTCTTCCAACTTCAAAAAAGCCAAGAGAGTC A C HDAC1 Ensembl:ENSG00000116478 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:32332117..32332217 32194978 MeRIP-seq:(Medium) rs1341194366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191360,Human_RBP_ID_221345,Human_RBP_ID_352505,Human_RBP_ID_3935677,Human_RBP_ID_5518769,Human_RBP_ID_9355936,Human_RBP_ID_17748908,Human_RBP_ID_18965168,Human_RBP_ID_22870800,Human_RBP_ID_24541447,Human_RBP_ID_26310756,Human_RBP_ID_27797738 Human_Splice_Rec_43308,Human_Splice_Rec_43309,Human_Splice_Rec_43378,Human_Splice_Rec_43379,Human_Splice_Rec_43389 RMVar_hsa_circ_116794,RMVar_hsa_circ_131229,RMVar_hsa_circ_110997,RMVar_hsa_circ_91934,RMVar_hsa_circ_131231,RMVar_hsa_circ_131233,RMVar_hsa_circ_81817,RMVar_hsa_circ_109004,RMVar_hsa_circ_131234,RMVar_hsa_circ_116341,RMVar_hsa_circ_131235,RMVar_hsa_circ_131237,RMVar_hsa_circ_80184,RMVar_hsa_circ_101227,RMVar_hsa_circ_90365,RMVar_hsa_circ_131238,RMVar_hsa_circ_131239,RMVar_hsa_circ_131240 88183 RMVar_ID_88183 Human_SNP_ID_8515439 m1A Human chr1 + 32332201 32332201 32332201 CTCTTCCAACTTCAAAAAAGCCAAGAGAGTCAAAACAGAGGATGAAAAAGAGAAAGACCCAGAGG CTCTTCCAACTTCAAAAAAGCCAAGAGAGTCAGAACAGAGGATGAAAAAGAGAAAGACCCAGAGG A G HDAC1 Ensembl:ENSG00000116478 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32332151..32332250;chr1:32332151..32332724 26863196 MeRIP-seq:(Medium) rs752320800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18128,Human_RBP_ID_191360,Human_RBP_ID_859562,Human_RBP_ID_2143434,Human_RBP_ID_3935677,Human_RBP_ID_5518769,Human_RBP_ID_8227977,Human_RBP_ID_9355936,Human_RBP_ID_10942240,Human_RBP_ID_17646330,Human_RBP_ID_18965168,Human_RBP_ID_22870800,Human_RBP_ID_24541447,Human_RBP_ID_26310756,Human_RBP_ID_27181573,Human_RBP_ID_27797738 Human_Splice_Rec_43309,Human_Splice_Rec_43379,Human_Splice_Rec_43389 RMVar_hsa_circ_116794,RMVar_hsa_circ_131229,RMVar_hsa_circ_110997,RMVar_hsa_circ_91934,RMVar_hsa_circ_131231,RMVar_hsa_circ_131233,RMVar_hsa_circ_81817,RMVar_hsa_circ_109004,RMVar_hsa_circ_131234,RMVar_hsa_circ_116341,RMVar_hsa_circ_131235,RMVar_hsa_circ_131237,RMVar_hsa_circ_80184,RMVar_hsa_circ_101227,RMVar_hsa_circ_90365,RMVar_hsa_circ_131238,RMVar_hsa_circ_131239,RMVar_hsa_circ_131240 88184 RMVar_ID_88184 Human_SNP_ID_8515776 m1A Human chr1 + 32333225 32333225 32333225 CAGGGCAGCTGTGCTGGGTGAGCTCTTCCAGGAGCCACCTTGCCACCCATTCTTCCCGTTCTTAA CAGGGCAGCTGTGCTGGGTGAGCTCTTCCAGGGGCCACCTTGCCACCCATTCTTCCCGTTCTTAA A G HDAC1 Ensembl:ENSG00000116478 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:32333176..32333350 32194978 MeRIP-seq:(Medium) rs1309692271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352512,Human_RBP_ID_5109523,Human_RBP_ID_8968965,Human_RBP_ID_10942249,Human_RBP_ID_17218049,Human_RBP_ID_17452462,Human_RBP_ID_23205849,Human_RBP_ID_24452251,Human_RBP_ID_26862539 Human_miRNA_ID_2696496 RMVar_hsa_circ_116794,RMVar_hsa_circ_131229,RMVar_hsa_circ_110997,RMVar_hsa_circ_91934,RMVar_hsa_circ_131231,RMVar_hsa_circ_131233,RMVar_hsa_circ_81817,RMVar_hsa_circ_109004,RMVar_hsa_circ_131234,RMVar_hsa_circ_116341,RMVar_hsa_circ_131235,RMVar_hsa_circ_131237,RMVar_hsa_circ_80184,RMVar_hsa_circ_86828,RMVar_hsa_circ_101227,RMVar_hsa_circ_90365,RMVar_hsa_circ_131238,RMVar_hsa_circ_131239,RMVar_hsa_circ_79289,RMVar_hsa_circ_131240,RMVar_hsa_circ_131241,RMVar_hsa_circ_131242 88185 RMVar_ID_88185 Human_SNP_ID_8516081 m1A Human chr1 + 32334316 32334316 32334316 AAAACCAACAACTGCCTTATGCAGGGGTGGGGACAGGGAAGGAGGTAGGGCCAGGGACAGGAGCA AAAACCAACAACTGCCTTATGCAGGGGTGGGGCCAGGGAAGGAGGTAGGGCCAGGGACAGGAGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32334265..32334541 26863196 MeRIP-seq:(Medium) rs939779567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131245 88186 RMVar_ID_88186 Human_SNP_ID_8516205 m1A Human chr1 + 32334702 32334702 32334702 TGGGGCCCTGCCTCTTCTTCTGAGGCTGCACTAGCCTCTGCCCCCTTGGCCTGGGGTTCCTGGCT TGGGGCCCTGCCTCTTCTTCTGAGGCTGCACTTGCCTCTGCCCCCTTGGCCTGGGGTTCCTGGCT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:32334601..32334800 26863410 MeRIP-seq:(Medium) rs1029011859 Functional Loss SNV dbSNP153 33..33 33 - - - 88187 RMVar_ID_88187 Human_SNP_ID_8516763 m1A Human chr1 - 32336102 32336102 32336102 GCGCCAGCCCCACCCCTCCGCCGGCCGGGCCGACCCCGCCGTACTATCCCCTGCGGCGCGAGCCC GCGCCAGCCCCACCCCTCCGCCGGCCGGGCCGCCCCCGCCGTACTATCCCCTGCGGCGCGAGCCC T G MARCKSL1 Ensembl:ENSG00000175130 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32335910..32336225;chr1:32334790..32336225;chr1:32335904..32336225 26863196 MeRIP-seq:(Medium) rs992820261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072678,Human_RBP_ID_5434025,Human_RBP_ID_5457535,Human_RBP_ID_5486138,Human_RBP_ID_17677610,Human_RBP_ID_19341759,Human_RBP_ID_22531940,Human_RBP_ID_23388360 Human_miRNA_ID_2145891,Human_miRNA_ID_2987326,Human_miRNA_ID_3021016 RMVar_hsa_circ_96359,RMVar_hsa_circ_131243 88188 RMVar_ID_88188 Human_SNP_ID_8516774 m1A Human chr1 - 32336123 32336123 32336123 CCCGGCACCCCTCCCCCTCGGGCGCCAGCCCCACCCCTCCGCCGGCCGGGCCGACCCCGCCGTAC CCCGGCACCCCTCCCCCTCGGGCGCCAGCCCCCCCCCTCCGCCGGCCGGGCCGACCCCGCCGTAC T G MARCKSL1 Ensembl:ENSG00000175130 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:32336024..32336229 26863410 MeRIP-seq:(Medium) rs948852732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072678,Human_RBP_ID_5413927,Human_RBP_ID_5434025,Human_RBP_ID_5457536,Human_RBP_ID_5486140,Human_RBP_ID_23388360 Human_miRNA_ID_2152682,Human_miRNA_ID_2800553,Human_miRNA_ID_3008681 RMVar_hsa_circ_96359,RMVar_hsa_circ_131243 88189 RMVar_ID_88189 Human_SNP_ID_8516780 m1A Human chr1 + 32336138 32336138 32336138 CCCGGCCGGCGGAGGGGTGGGGCTGGCGCCCGAGGGGGAGGGGTGCCGGGGGAAGCCGAGCTGCA CCCGGCCGGCGGAGGGGTGGGGCTGGCGCCCGGGGGGGAGGGGTGCCGGGGGAAGCCGAGCTGCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:32335926..32336250;chr1:32335985..32336233 26863410 MeRIP-seq:(Medium) rs1363607826 Functional Loss SNV dbSNP153 33..33 33 - - - 88190 RMVar_ID_88190 Human_SNP_ID_8516782 m1A Human chr1 + 32336144 32336144 32336144 CGGCGGAGGGGTGGGGCTGGCGCCCGAGGGGGAGGGGTGCCGGGGGAAGCCGAGCTGCACCTCCG CGGCGGAGGGGTGGGGCTGGCGCCCGAGGGGGGGGGGTGCCGGGGGAAGCCGAGCTGCACCTCCG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:32336042..32336229 26863410 MeRIP-seq:(Medium) rs1044849577 Functional Loss SNV dbSNP153 33..33 33 - - - 88191 RMVar_ID_88191 Human_SNP_ID_8521724 m1A Human chr1 + 32355671 32355671 32355671 GTGATGATTTGAAAGGTGTCCAGTGTGGCTGCACAAGTGATGTGAAGAAGCCATTGATGAGGTTT GTGATGATTTGAAAGGTGTCCAGTGTGGCTGCCCAAGTGATGTGAAGAAGCCATTGATGAGGTTT A C TSSK3 Ensembl:ENSG00000162526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32355634..32355829 26863196 MeRIP-seq:(Medium) rs1477747017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23388378 88192 RMVar_ID_88192 Human_SNP_ID_8525436 m1A Human chr1 - 32368514 32368514 32368514 AAGCACGGACATCAGTGAGGACTGGGAGAAAGACTTTGACTTGGACATGACTGAAGAGGAGGTGC AAGCACGGACATCAGTGAGGACTGGGAGAAAGTCTTTGACTTGGACATGACTGAAGAGGAGGTGC T A BSDC1 Ensembl:ENSG00000160058 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32368376..32368576 26863196 MeRIP-seq:(Medium) rs979988472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224354,Human_RBP_ID_352655,Human_RBP_ID_1429419,Human_RBP_ID_3933164,Human_RBP_ID_4045813,Human_RBP_ID_8748219,Human_RBP_ID_9358540,Human_RBP_ID_10942759,Human_RBP_ID_18410111,Human_RBP_ID_18967908,Human_RBP_ID_22871754,Human_RBP_ID_23205083,Human_RBP_ID_24541632,Human_RBP_ID_27181641,Human_RBP_ID_27797740 Human_Splice_Rec_43434,Human_Splice_Rec_43435,Human_Splice_Rec_43456,Human_Splice_Rec_43457,Human_Splice_Rec_43476,Human_Splice_Rec_43490,Human_Splice_Rec_43491,Human_Splice_Rec_43508,Human_Splice_Rec_43509,Human_Splice_Rec_43528,Human_Splice_Rec_43529,Human_Splice_Rec_43532,Human_Splice_Rec_43550 RMVar_hsa_circ_49496,RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_131246 88193 RMVar_ID_88193 Human_SNP_ID_8527370 m1A Human chr1 - 32376352 32376352 32376352 GCCCAGAGCCCAGGCCTCCAGCCAGAGTAGAGACTCTGAGGGAGGAGGCGCCCACAGACTTACGG GCCCAGAGCCCAGGCCTCCAGCCAGAGTAGAGTCTCTGAGGGAGGAGGCGCCCACAGACTTACGG T A BSDC1 Ensembl:ENSG00000160058 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:32376301..32376546 32194978 MeRIP-seq:(Medium) rs1455023732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10943080,Human_RBP_ID_26862645,Human_RBP_ID_27181646 Human_Splice_Rec_43433,Human_Splice_Rec_43453,Human_Splice_Rec_43475,Human_Splice_Rec_43489,Human_Splice_Rec_43507,Human_Splice_Rec_43527,Human_Splice_Rec_43549 RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_313977,RMVar_hsa_circ_358249 88194 RMVar_ID_88194 Human_SNP_ID_8527478 m1A Human chr1 - 32376602 32376602 32376602 GAGAATCTGGTGACTTCAGTTGAGCCCCCAGCAGAGGTGACTCCATCAGAGAGCAGTGAGAGCAT GAGAATCTGGTGACTTCAGTTGAGCCCCCAGCGGAGGTGACTCCATCAGAGAGCAGTGAGAGCAT T C BSDC1 Ensembl:ENSG00000160058 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32376551..32376635 26863196 MeRIP-seq:(Medium) rs1326301869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101964,Human_RBP_ID_191361,Human_RBP_ID_3935682,Human_RBP_ID_9358543,Human_RBP_ID_18965172,Human_RBP_ID_23112653,Human_RBP_ID_24541060 RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_313977,RMVar_hsa_circ_358249 88195 RMVar_ID_88195 Human_SNP_ID_8530120 m1A Human chr1 + 32386892 32386892 32386892 CAGGTCCCGCTTCATAAACTCCAAGGCTTCAGAGGACTGTGGGAAGACAGAGAGGGATGCCAGGG CAGGTCCCGCTTCATAAACTCCAAGGCTTCAGTGGACTGTGGGAAGACAGAGAGGGATGCCAGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32386776..32386932 26863196 MeRIP-seq:(Medium) rs201967424 Functional Loss SNV dbSNP153 33..33 33 - - - 88196 RMVar_ID_88196 Human_SNP_ID_8556917 m1A Human chr1 + 32500583 32500583 32500583 CGGCCGAGAGCGAGGCCGGAGGCGCCAAGCCGAGCGGGCGCCATTTGCAGCCTGGGGCGCAGCAG CGGCCGAGAGCGAGGCCGGAGGCGCCAAGCCGGGCGGGCGCCATTTGCAGCCTGGGGCGCAGCAG A G AL033529.1 Ensembl:ENSG00000254553 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32500415..32500708 26863196 MeRIP-seq:(Medium) rs1156647001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131252,RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251 88197 RMVar_ID_88197 Human_SNP_ID_8556919 m1A Human chr1 - 32500594 32500594 32500594 CAGCGCTGCAGCTGCTGCGCCCCAGGCTGCAAATGGCGCCCGCTCGGCTTGGCGCCTCCGGCCTC CAGCGCTGCAGCTGCTGCGCCCCAGGCTGCAATTGGCGCCCGCTCGGCTTGGCGCCTCCGGCCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32500433..32500612 26863196 MeRIP-seq:(Medium) rs1343702021 Functional Loss SNV dbSNP153 33..33 33 - - - 88198 RMVar_ID_88198 Human_SNP_ID_8566529 m1A Human chr1 + 32539548 32539532 32539549 AACCAGGAATCTTCCCTCGGCCCGCGCGCGCGACCGGCCGGTGCGCCGCGGCCCGCGGTAAGTGG AACCAGGAATCTTCCCT_________________CGGCCGGTGCGCCGCGGCCCGCGGTAAGTGG TCGGCCCGCGCGCGCGAC T ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32539498..32539626 26863196 MeRIP-seq:(Medium) rs1457404032 Functional Loss DEL dbSNP153 18..34 33 - - - Human_Splice_Rec_43633,Human_Splice_Rec_43641 RMVar_hsa_circ_131252,RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_102825,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131254,RMVar_hsa_circ_131255 88199 RMVar_ID_88199 Human_SNP_ID_8566675 m1A Human chr1 - 32539777 32539777 32539777 CGGGCCGGGCGGCGAGGCGGGCGCGGGCGGCGACGGCGCGGCCATTGTCCCGCAGCCCCTCCCGG CGGGCCGGGCGGCGAGGCGGGCGCGGGCGGCGGCGGCGCGGCCATTGTCCCGCAGCCCCTCCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32539768..32539983 26863196 MeRIP-seq:(Medium) rs1218215344 Functional Loss SNV dbSNP153 33..33 33 - - - 88200 RMVar_ID_88200 Human_SNP_ID_8580043 m1A Human chr1 + 32592981 32592981 32592981 TCAGTCTCACCTCCTGCAGCAACTGAACGAGCAGCGCAGGCAAGATGTATTTTGTGACTGCAGTA TCAGTCTCACCTCCTGCAGCAACTGAACGAGCGGCGCAGGCAAGATGTATTTTGTGACTGCAGTA A G ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32592917..32592983 26863196 MeRIP-seq:(Medium) rs148381621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10943984 Human_Splice_Rec_43622,Human_Splice_Rec_43636,Human_Splice_Rec_43644 RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_131259,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257,RMVar_hsa_circ_131261,RMVar_hsa_circ_272817,RMVar_hsa_circ_272939,RMVar_hsa_circ_131260 88201 RMVar_ID_88201 Human_SNP_ID_8594989 m1A Human chr1 - 32650503 32650503 32650503 GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGAGATTACAATTTGACTGAAGAACAGAAGGCGAT GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGTGATTACAATTTGACTGAAGAACAGAAGGCGAT T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:32650402..32650520;chr1:32650382..32650704 26863196 MeRIP-seq:(Medium) rs758800199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429440,Human_RBP_ID_1745669,Human_RBP_ID_10944936,Human_RBP_ID_18409923,Human_RBP_ID_22023130,Human_RBP_ID_23388650,Human_RBP_ID_27797747 Human_Splice_Rec_43649,Human_Splice_Rec_43651,Human_Splice_Rec_43663,Human_Splice_Rec_43669,Human_Splice_Rec_43693,Human_Splice_Rec_43705,Human_Splice_Rec_43717,Human_Splice_Rec_43727,Human_Splice_Rec_43749,Human_Splice_Rec_43759,Human_Splice_Rec_43769 Human_miRNA_ID_2231723 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 88202 RMVar_ID_88202 Human_SNP_ID_8594990 m1A Human chr1 - 32650503 32650503 32650503 GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGAGATTACAATTTGACTGAAGAACAGAAGGCGAT GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGGGATTACAATTTGACTGAAGAACAGAAGGCGAT T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:32650402..32650520;chr1:32650382..32650704 26863196 MeRIP-seq:(Medium) rs758800199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429440,Human_RBP_ID_1745669,Human_RBP_ID_10944936,Human_RBP_ID_18409923,Human_RBP_ID_22023130,Human_RBP_ID_23388650,Human_RBP_ID_27797747 Human_Splice_Rec_43649,Human_Splice_Rec_43651,Human_Splice_Rec_43663,Human_Splice_Rec_43669,Human_Splice_Rec_43693,Human_Splice_Rec_43705,Human_Splice_Rec_43717,Human_Splice_Rec_43727,Human_Splice_Rec_43749,Human_Splice_Rec_43759,Human_Splice_Rec_43769 Human_miRNA_ID_2231723 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 88203 RMVar_ID_88203 Human_SNP_ID_8594991 m1A Human chr1 - 32650503 32650503 32650503 GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGAGATTACAATTTGACTGAAGAACAGAAGGCGAT GCAGTCATGGCGCAGGAAGAGGAAGATGTTAGCGATTACAATTTGACTGAAGAACAGAAGGCGAT T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:32650402..32650520;chr1:32650382..32650704 26863196 MeRIP-seq:(Medium) rs758800199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429440,Human_RBP_ID_1745669,Human_RBP_ID_10944936,Human_RBP_ID_18409923,Human_RBP_ID_22023130,Human_RBP_ID_23388650,Human_RBP_ID_27797747 Human_Splice_Rec_43649,Human_Splice_Rec_43651,Human_Splice_Rec_43663,Human_Splice_Rec_43669,Human_Splice_Rec_43693,Human_Splice_Rec_43705,Human_Splice_Rec_43717,Human_Splice_Rec_43727,Human_Splice_Rec_43749,Human_Splice_Rec_43759,Human_Splice_Rec_43769 Human_miRNA_ID_2231723 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 88204 RMVar_ID_88204 Human_SNP_ID_8595328 m1A Human chr1 + 32651267 32651267 32651267 GCGAGCTCTTGCAGCCTCCCCGCCCCTCCCGCAACGCTCGACCCCAGGATTCCCCCGGCTCGCCT GCGAGCTCTTGCAGCCTCCCCGCCCCTCCCGCCACGCTCGACCCCAGGATTCCCCCGGCTCGCCT A C RBBP4 Ensembl:ENSG00000162521 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32651201..32651381;chr1:32651201..32651387;chr1:32651201..32651376;chr1:32651201..32651395;chr1:32651201..32651379 26863196 MeRIP-seq:(Medium) rs971294145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224419,Human_RBP_ID_352728,Human_RBP_ID_4073824,Human_RBP_ID_17338096 Human_Splice_Rec_43771,Human_Splice_Rec_43793,Human_Splice_Rec_43801,Human_Splice_Rec_43823,Human_Splice_Rec_43829,Human_Splice_Rec_43837,Human_Splice_Rec_43845,Human_Splice_Rec_43863,Human_Splice_Rec_43867,Human_Splice_Rec_43869,Human_Splice_Rec_43891 88205 RMVar_ID_88205 Human_SNP_ID_8595329 m1A Human chr1 + 32651267 32651267 32651267 GCGAGCTCTTGCAGCCTCCCCGCCCCTCCCGCAACGCTCGACCCCAGGATTCCCCCGGCTCGCCT GCGAGCTCTTGCAGCCTCCCCGCCCCTCCCGCGACGCTCGACCCCAGGATTCCCCCGGCTCGCCT A G RBBP4 Ensembl:ENSG00000162521 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32651201..32651381;chr1:32651201..32651387;chr1:32651201..32651376;chr1:32651201..32651395;chr1:32651201..32651379 26863196 MeRIP-seq:(Medium) rs971294145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224419,Human_RBP_ID_352728,Human_RBP_ID_4073824,Human_RBP_ID_17338096 Human_Splice_Rec_43771,Human_Splice_Rec_43793,Human_Splice_Rec_43801,Human_Splice_Rec_43823,Human_Splice_Rec_43829,Human_Splice_Rec_43837,Human_Splice_Rec_43845,Human_Splice_Rec_43863,Human_Splice_Rec_43867,Human_Splice_Rec_43869,Human_Splice_Rec_43891 88206 RMVar_ID_88206 Human_SNP_ID_8595339 m1A Human chr1 + 32651275 32651275 32651275 TTGCAGCCTCCCCGCCCCTCCCGCAACGCTCGACCCCAGGATTCCCCCGGCTCGCCTGCCCGCCA TTGCAGCCTCCCCGCCCCTCCCGCAACGCTCGGCCCCAGGATTCCCCCGGCTCGCCTGCCCGCCA A G RBBP4 Ensembl:ENSG00000162521 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32651226..32651389 26863196 MeRIP-seq:(Medium) rs1352111278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224419,Human_RBP_ID_352728,Human_RBP_ID_4073824,Human_RBP_ID_26310765 Human_Splice_Rec_43771,Human_Splice_Rec_43793,Human_Splice_Rec_43801,Human_Splice_Rec_43823,Human_Splice_Rec_43829,Human_Splice_Rec_43837,Human_Splice_Rec_43845,Human_Splice_Rec_43863,Human_Splice_Rec_43867,Human_Splice_Rec_43869,Human_Splice_Rec_43891 88207 RMVar_ID_88207 Human_SNP_ID_8595376 m1A Human chr1 - 32651324 32651324 32651324 CACTGCCCTCCTGGGTCGGCCCCGGCACCCTCACCTTCCTTGTCGGCCATGGCGGGCAGGCGAGC CACTGCCCTCCTGGGTCGGCCCCGGCACCCTCCCCTTCCTTGTCGGCCATGGCGGGCAGGCGAGC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:32651201..32651388 26863196 MeRIP-seq:(Medium) rs530899496 Functional Loss SNV dbSNP153 33..33 33 - - - 88208 RMVar_ID_88208 Human_SNP_ID_8595609 m1A Human chr1 + 32651903 32651903 32651903 TTCCGTTTGTTTGCTAACTTAAATTTGTTTTTAAAAATTTTAGCAGCCTTCGACGACGCAGTGGA TTCCGTTTGTTTGCTAACTTAAATTTGTTTTTGAAAATTTTAGCAGCCTTCGACGACGCAGTGGA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:32651901..32651950 26863196 MeRIP-seq:(Medium) rs753835233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1745671,Human_RBP_ID_26862689 88209 RMVar_ID_88209 Human_SNP_ID_8605265 m1A Human chr1 + 32683772 32683772 32683772 CTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTATAAGTGCCTGCCACTATGCCCGGCTAATTTTT CTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTGTAAGTGCCTGCCACTATGCCCGGCTAATTTTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs545280403 Functional Loss SNV dbSNP153 33..33 33 - - - 88210 RMVar_ID_88210 Human_SNP_ID_8608796 m1A Human chr1 - 32695370 32695370 32695370 AGATGGCCTAAGGGAGGAGATCCGGCTGGTCAAGCAGAAGCTTTTCAAAGTGACAAAGGAATGTG AGATGGCCTAAGGGAGGAGATCCGGCTGGTCAGGCAGAAGCTTTTCAAAGTGACAAAGGAATGTG T C SYNC Ensembl:ENSG00000162520 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32695319..32695391 26863196 MeRIP-seq:(Medium) rs968590087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37438,RMVar_hsa_circ_24496,RMVar_hsa_circ_131284,RMVar_hsa_circ_310874 88211 RMVar_ID_88211 Human_SNP_ID_8608955 m1A Human chr1 - 32695764 32695764 32695764 GGAATCCAGAGGAGACAGTGTGTGTGGAGGAAACCACGGAGCCAGATCGGATACAGTTTGTGGAG GGAATCCAGAGGAGACAGTGTGTGTGGAGGAAGCCACGGAGCCAGATCGGATACAGTTTGTGGAG T C SYNC Ensembl:ENSG00000162520 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32695548..32695798 26863196 MeRIP-seq:(Medium) rs1367860883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37438,RMVar_hsa_circ_24496,RMVar_hsa_circ_131284,RMVar_hsa_circ_310874 88212 RMVar_ID_88212 Human_SNP_ID_8623096 m1A Human chr1 - 32751654 32751654 32751654 TACATGCTGCTCCTCCATGAAGTCTTCCTTGCACCCCCTCTTCCCCCAGCTCAGTGCTTCCTTAA TACATGCTGCTCCTCCATGAAGTCTTCCTTGCTCCCCCTCTTCCCCCAGCTCAGTGCTTCCTTAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32751649..32751718 26863196 MeRIP-seq:(Medium) rs754947304 Functional Loss SNV dbSNP153 33..33 33 - - - 88213 RMVar_ID_88213 Human_SNP_ID_8624850 m1A Human chr1 + 32757439 32757439 32757439 CCAGGGGAGAGGTGATGAGGTGAGGGCTGGGGACAGGGTGGGGGTTGTGGGAGTGGAGAGGAGTG CCAGGGGAGAGGTGATGAGGTGAGGGCTGGGGGCAGGGTGGGGGTTGTGGGAGTGGAGAGGAGTG A G KIAA1522 Ensembl:ENSG00000162522 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32757437..32757536 26863196 MeRIP-seq:(Medium) rs1209714258 Functional Loss SNV dbSNP153 33..33 33 - - - 88214 RMVar_ID_88214 Human_SNP_ID_8627276 m1A Human chr1 + 32767871 32767871 32767871 GCCAGGGTCTGCAGTGGATGAGCACCAGGACAACGTCTTCTTTCCCAGTGGGCGACCCCCCCACC GCCAGGGTCTGCAGTGGATGAGCACCAGGACAGCGTCTTCTTTCCCAGTGGGCGACCCCCCCACC A G KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:32767821..32767921 32194978 MeRIP-seq:(Medium) rs1217412248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27397819 Human_Splice_Rec_44006,Human_Splice_Rec_44007,Human_Splice_Rec_44018,Human_Splice_Rec_44019,Human_Splice_Rec_44024,Human_Splice_Rec_44025,Human_Splice_Rec_44036,Human_Splice_Rec_44037,Human_Splice_Rec_44044,Human_Splice_Rec_44045 88215 RMVar_ID_88215 Human_SNP_ID_8628044 m1A Human chr1 + 32770050 32770050 32770050 CGGAGGCGGAGGCTGGCGCTGAGACAGAGGCCATGCTGCAGCGCCACATTGACCGTGTCTACCGG CGGAGGCGGAGGCTGGCGCTGAGACAGAGGCCGTGCTGCAGCGCCACATTGACCGTGTCTACCGG A G KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12730560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27555332 GWAS_ID_11152,GWAS_ID_11153,GWAS_ID_11154,GWAS_ID_11155,GWAS_ID_11156,GWAS_ID_11157 88216 RMVar_ID_88216 Human_SNP_ID_8628218 m1A Human chr1 + 32770432 32770432 32770432 CCACCCATCCTCCTCCAGTGACACCTGGAGCCACTCTCAATCCTCCGACACCATTGTGTCTGACG CCACCCATCCTCCTCCAGTGACACCTGGAGCCCCTCTCAATCCTCCGACACCATTGTGTCTGACG A C KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32770333..32770437 26863196 MeRIP-seq:(Medium) rs1257437352 Functional Loss SNV dbSNP153 33..33 33 - - - 88217 RMVar_ID_88217 Human_SNP_ID_8628523 m1A Human chr1 + 32771099 32771099 32771099 CTCACGTCTTTATGTTCCTCCTCCTCTGACCCAGCCCCCTCAGACCGCTCTGGGCCACAGATATT CTCACGTCTTTATGTTCCTCCTCCTCTGACCCGGCCCCCTCAGACCGCTCTGGGCCACAGATATT A G KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32771052..32771299 26863196 MeRIP-seq:(Medium) rs759435830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352873,Human_RBP_ID_745402,Human_RBP_ID_5125244,Human_RBP_ID_17071115,Human_RBP_ID_17338910,Human_RBP_ID_17456428,Human_RBP_ID_17558356,Human_RBP_ID_18572392,Human_RBP_ID_18929549,Human_RBP_ID_19441246 88218 RMVar_ID_88218 Human_SNP_ID_8628576 m1A Human chr1 + 32771225 32771225 32771225 CCACCTCCCTCCAAGCCCAGGAGCCCTAACCCAGCTGCCCCTGCTCTAGCCGCCCCTGCTGTGGT CCACCTCCCTCCAAGCCCAGGAGCCCTAACCCTGCTGCCCCTGCTCTAGCCGCCCCTGCTGTGGT A T KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32771176..32771298 26863196 MeRIP-seq:(Medium) rs376897230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125688,Human_RBP_ID_17071116,Human_RBP_ID_17338098,Human_RBP_ID_17456429,Human_RBP_ID_18929550,Human_RBP_ID_22141939,Human_RBP_ID_22862277 88219 RMVar_ID_88219 Human_SNP_ID_8628804 m1A Human chr1 + 32771690 32771690 32771690 ATTCAGCCCCCGGGTAGCCCAGACCCTCCTCCAGCTCCGCCAGCCCCAGCTCCTGCTAGTTCCGC ATTCAGCCCCCGGGTAGCCCAGACCCTCCTCCTGCTCCGCCAGCCCCAGCTCCTGCTAGTTCCGC A T KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:32771566..32771900 26863196 MeRIP-seq:(Medium) rs749093534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102122,Human_RBP_ID_352881,Human_RBP_ID_17071463,Human_RBP_ID_17338915 Human_miRNA_ID_1355222 88220 RMVar_ID_88220 Human_SNP_ID_8629486 m1A Human chr1 - 32773712 32773711 32773713 TGCCTCTGAAGTGCTGGGGGCCCACCCACCCCAGTGTGGTCAAGGAGGCAAGGGGCAGGTGCTTG TGCCTCTGAAGTGCTGGGGGCCCACCCACCC__GTGTGGTCAAGGAGGCAAGGGGCAGGTGCTTG CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32773661..32773789 26863196 MeRIP-seq:(Medium) rs1350603413 Functional Loss DEL dbSNP153 32..33 33 - - - 88221 RMVar_ID_88221 Human_SNP_ID_8631146 m1A Human chr1 - 32780184 32780184 32780184 TGTGGTGAGCGGCCTGGTACAGTTCGTGCCCAAGGAGGAACTGCAGGACAGGCTGGTAGTGGTGC TGTGGTGAGCGGCCTGGTACAGTTCGTGCCCAGGGAGGAACTGCAGGACAGGCTGGTAGTGGTGC T C YARS1 Ensembl:ENSG00000134684 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1368158146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352939,Human_RBP_ID_742831,Human_RBP_ID_1429590,Human_RBP_ID_1745774,Human_RBP_ID_4094482,Human_RBP_ID_5519748,Human_RBP_ID_5812683,Human_RBP_ID_8308743,Human_RBP_ID_8748269,Human_RBP_ID_8969085,Human_RBP_ID_9252872,Human_RBP_ID_9270021,Human_RBP_ID_10946618,Human_RBP_ID_18468726,Human_RBP_ID_22427105,Human_RBP_ID_26310771,Human_RBP_ID_27799986 Human_Splice_Rec_44056,Human_Splice_Rec_44057,Human_Splice_Rec_44080,Human_Splice_Rec_44081,Human_Splice_Rec_44090,Human_Splice_Rec_44091,Human_Splice_Rec_44100,Human_Splice_Rec_44101,Human_Splice_Rec_44124 Human_miRNA_ID_2224717,Human_miRNA_ID_2224718 RMVar_hsa_circ_97767,RMVar_hsa_circ_116445,RMVar_hsa_circ_125184,RMVar_hsa_circ_106365,RMVar_hsa_circ_65189,RMVar_hsa_circ_131288,RMVar_hsa_circ_89944,RMVar_hsa_circ_94780,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_131286,RMVar_hsa_circ_131287,RMVar_hsa_circ_282615,RMVar_hsa_circ_131285,RMVar_hsa_circ_331832,RMVar_hsa_circ_278410,RMVar_hsa_circ_131294,RMVar_hsa_circ_131292,RMVar_hsa_circ_43532,RMVar_hsa_circ_131293,RMVar_hsa_circ_95633 88222 RMVar_ID_88222 Human_SNP_ID_8631733 m1A Human chr1 - 32782353 32782353 32782353 GGGCCGACATCATCAGGAGAGAGAGCTTGTCAATGAGCCTTGGAAAAATGCCTGTCTTAAATTGA GGGCCGACATCATCAGGAGAGAGAGCTTGTCAGTGAGCCTTGGAAAAATGCCTGTCTTAAATTGA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32782350..32782473 26863196 MeRIP-seq:(Medium) rs561400916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5518771,Human_RBP_ID_10946717,Human_RBP_ID_18572438 RMVar_hsa_circ_97767,RMVar_hsa_circ_116445,RMVar_hsa_circ_125184,RMVar_hsa_circ_106365,RMVar_hsa_circ_65189,RMVar_hsa_circ_131288,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_131286,RMVar_hsa_circ_131287,RMVar_hsa_circ_331832,RMVar_hsa_circ_278410,RMVar_hsa_circ_43532,RMVar_hsa_circ_131293 88223 RMVar_ID_88223 Human_SNP_ID_8639331 m1A Human chr1 - 32811027 32811027 32811027 AGGAGGTTCTGGGGGAAGAGAAGCTGAAGGAGATACTGAAGGAGCGGGAACTTAAAATTTACTGG AGGAGGTTCTGGGGGAAGAGAAGCTGAAGGAGGTACTGAAGGAGCGGGAACTTAAAATTTACTGG T C YARS1 Ensembl:ENSG00000134684 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr1:32810976..32811075;chr1:32810976..32811120 26863196 MeRIP-seq:(Medium) rs748003708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429700,Human_RBP_ID_1745826,Human_RBP_ID_3935704,Human_RBP_ID_4094510,Human_RBP_ID_5812894,Human_RBP_ID_8308827,Human_RBP_ID_8754908,Human_RBP_ID_9252890,Human_RBP_ID_9270034,Human_RBP_ID_10947636,Human_RBP_ID_17749144,Human_RBP_ID_22429224,Human_RBP_ID_23389039,Human_RBP_ID_26313832 Human_Splice_Rec_44062,Human_Splice_Rec_44106,Human_Splice_Rec_44126 RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_374232,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_354237,RMVar_hsa_circ_131300,RMVar_hsa_circ_323742,RMVar_hsa_circ_131303,RMVar_hsa_circ_131304,RMVar_hsa_circ_287408 88224 RMVar_ID_88224 Human_SNP_ID_8639972 m1A Human chr1 - 32813645 32813645 32813645 AATTGGCTATGAAAGGAAGGAGAGTGAGTTAGAGGCATGTAAACCAAAAAGTATCTGAGGCCAGG AATTGGCTATGAAAGGAAGGAGAGTGAGTTAGCGGCATGTAAACCAAAAAGTATCTGAGGCCAGG T G YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32813643..32814370 26863196 MeRIP-seq:(Medium) rs922194860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5812915,Human_RBP_ID_8939961,Human_RBP_ID_10947735,Human_RBP_ID_23263280 RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 88225 RMVar_ID_88225 Human_SNP_ID_8640024 m1A Human chr1 - 32813907 32813907 32813907 GAACAGTTGCAAAGAAAGCTAAGCAGGCAGAGACGAGGAAAACTAAGAATAAAATAAAGGAGACC GAACAGTTGCAAAGAAAGCTAAGCAGGCAGAGCCGAGGAAAACTAAGAATAAAATAAAGGAGACC T G YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32813905..32814164 26863196 MeRIP-seq:(Medium) rs1275645296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 88226 RMVar_ID_88226 Human_SNP_ID_8640839 m1A Human chr1 + 32817159 32817159 32817159 AAAATCACTGAACCTCGGGCTCCTAATCCCCAACGGCGCATTTCCAACCCCCAGGCCTGACCTGC AAAATCACTGAACCTCGGGCTCCTAATCCCCAGCGGCGCATTTCCAACCCCCAGGCCTGACCTGC A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:32817156..32817350 26863410 MeRIP-seq:(Medium) rs1426669918 Functional Loss SNV dbSNP153 33..33 33 - - - 88227 RMVar_ID_88227 Human_SNP_ID_8640882 m1A Human chr1 + 32817243 32817243 32817243 GCAGTTTCTCTTCAGGGCTGGGAGCGTCCCCCATGGCTCCGCTACCCCTGCTTCCCCCGCTCAGC GCAGTTTCTCTTCAGGGCTGGGAGCGTCCCCCCTGGCTCCGCTACCCCTGCTTCCCCCGCTCAGC A C S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32817181..32817335 26863196 MeRIP-seq:(Medium) rs1032889843 Functional Loss SNV dbSNP153 33..33 33 - - - 88228 RMVar_ID_88228 Human_SNP_ID_8640884 m1A Human chr1 - 32817253 32817253 32817253 CTGGTGCCGGGCTGAGCGGGGGAAGCAGGGGTAGCGGAGCCATGGGGGACGCTCCCAGCCCTGAA CTGGTGCCGGGCTGAGCGGGGGAAGCAGGGGTGGCGGAGCCATGGGGGACGCTCCCAGCCCTGAA T C YARS1 Ensembl:ENSG00000134684 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:32817119..32817350 26863196 MeRIP-seq:(Medium) rs990086732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20106,Human_RBP_ID_221988,Human_RBP_ID_803161,Human_RBP_ID_859196,Human_RBP_ID_1255236,Human_RBP_ID_4046337,Human_RBP_ID_5312444,Human_RBP_ID_8754910,Human_RBP_ID_9252893,Human_RBP_ID_9318818,Human_RBP_ID_22427110,Human_RBP_ID_22531943,Human_RBP_ID_23389057,Human_RBP_ID_26862877,Human_RBP_ID_27799993 Human_Splice_Rec_44061,Human_Splice_Rec_44105,Human_Splice_Rec_44125 RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 88229 RMVar_ID_88229 Human_SNP_ID_8641438 m1A Human chr1 + 32819083 32819080 32819084 GCAGTAGGTTTTCTGAGGTGAGATAAAAATAGAAAGGGAACCAGTTTCTGAGGTTGCAACCAGGA GCAGTAGGTTTTCTGAGGTGAGATAAAAAT____AGGGAACCAGTTTCTGAGGTTGCAACCAGGA TAGAA T S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32819076..32819268 26863196 MeRIP-seq:(Medium) rs1172280096 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 88230 RMVar_ID_88230 Human_SNP_ID_8660539 m1A Human chr1 - 32895662 32895662 32895662 CCTGTGCCCTCGGCCTCTTGGCCTCCATCGCCATGACCTTTGCCACCCAGGGCAAGGCACTGCTG CCTGTGCCCTCGGCCTCTTGGCCTCCATCGCCCTGACCTTTGCCACCCAGGGCAAGGCACTGCTG T G TMEM54 Ensembl:ENSG00000121900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32895611..32895707 26863196 MeRIP-seq:(Medium) rs1339478530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353023,Human_RBP_ID_26798092 Human_Splice_Rec_44300,Human_Splice_Rec_44326,Human_Splice_Rec_44336 88231 RMVar_ID_88231 Human_SNP_ID_8660561 m1A Human chr1 + 32895713 32895713 32895713 GCCGAGGGCACAGGTCAGAGAAAGGAGAGCACAGGCCACGCTCGAGCTAAACACTGTCCAGCGCT GCCGAGGGCACAGGTCAGAGAAAGGAGAGCACGGGCCACGCTCGAGCTAAACACTGTCCAGCGCT A G HPCA Ensembl:ENSG00000121905 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:32895551..32895750 32194978 MeRIP-seq:(Medium) rs1373240098 Functional Loss SNV dbSNP153 33..33 33 - - - 88232 RMVar_ID_88232 Human_SNP_ID_8677509 m1A Human chr1 - 32964099 32964099 32964099 GCACAAGTACGAGGAGTTCATGCTGCGCCGCTACCTAGCCTCGGACCCCGACTGCCGCTGGTGCC GCACAAGTACGAGGAGTTCATGCTGCGCCGCTGCCTAGCCTCGGACCCCGACTGCCGCTGGTGCC T C RNF19B Ensembl:ENSG00000116514 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:32949719..32964439 26863196 MeRIP-seq:(Medium) rs1379416426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8754911,Human_RBP_ID_9270038 Human_Splice_Rec_44343,Human_Splice_Rec_44359,Human_Splice_Rec_44375 RMVar_hsa_circ_103360,RMVar_hsa_circ_131322,RMVar_hsa_circ_269695 88233 RMVar_ID_88233 Human_SNP_ID_8677538 m1A Human chr1 - 32964192 32964192 32964192 AAGCGAGAGCAGGGTGCCCATCAGCTGCCCCGAGTGCAGCGAGCGACTCAACCCGCACGACATCC AAGCGAGAGCAGGGTGCCCATCAGCTGCCCCGGGTGCAGCGAGCGACTCAACCCGCACGACATCC T C RNF19B Ensembl:ENSG00000116514 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cells, overexperss TRMT6;HTR8/Svneo,Normoxia chr1:32964143..32964242 29072297,32194978 m1A-MAP:(High) - Functional Loss SNV HGVD 33..33 33 - - - RMVar_hsa_circ_103360,RMVar_hsa_circ_131322,RMVar_hsa_circ_269695 88234 RMVar_ID_88234 Human_SNP_ID_8677766 m1A Human chr1 + 32964773 32964764 32964773 AGCGCCCCTCAGCCAGCGCCCGGCCGCCGCCGACGCCGCCACCACCGCCTCAACCGCCCTCCCGG AGCGCCCCTCAGCCAGCGCCCGGC_________CGCCGCCACCACCGCCTCAACCGCCCTCCCGG CCGCCGCCGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:32964520..32964872;chr1:32964525..32964862;chr1:32964536..32964833 26863196 MeRIP-seq:(Medium) rs1312436795 Functional Loss DEL dbSNP153 25..33 33 - - - 88235 RMVar_ID_88235 Human_SNP_ID_8685748 m1A Human chr1 + 32995287 32995287 32995287 CTCATTTCATCCATCCCTGACTGGACACTCTCACTGGACACCATTCCCTTTCCAGCCTCCATGCC CTCATTTCATCCATCCCTGACTGGACACTCTCTCTGGACACCATTCCCTTTCCAGCCTCCATGCC A T AL020995.1 Ensembl:ENSG00000236065 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32995243..32995308 26863196 MeRIP-seq:(Medium) rs1475074113 Functional Loss SNV dbSNP153 33..33 33 - - - 88236 RMVar_ID_88236 Human_SNP_ID_8685898 m1A Human chr1 + 32995956 32995956 32995956 CTGATTTCAGATGTATACCTCTGTGGGGCCTTAGGCAGCACTCATTTCTTCTTTTCCTTTTCTTC CTGATTTCAGATGTATACCTCTGTGGGGCCTTGGGCAGCACTCATTTCTTCTTTTCCTTTTCTTC A G AL020995.1 Ensembl:ENSG00000236065 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:32995907..32996012 26863196 MeRIP-seq:(Medium) rs890451813 Functional Loss SNV dbSNP153 33..33 33 - - - 88237 RMVar_ID_88237 Human_SNP_ID_8690644 m1A Human chr1 - 33013237 33013237 33013237 ATGCATCCCAGACCCCCGATGTCGTGTTCGCAAGCATCCTAGCAGCCTTCTCCAAAGCCACATGT ATGCATCCCAGACCCCCGATGTCGTGTTCGCAGGCATCCTAGCAGCCTTCTCCAAAGCCACATGT T C AK2 Ensembl:ENSG00000004455 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr1:33013201..33013275;chr1:33013176..33013275 26863196 MeRIP-seq:(Medium) rs1259851576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353149,Human_RBP_ID_741261,Human_RBP_ID_1429785,Human_RBP_ID_10949595,Human_RBP_ID_22430423,Human_RBP_ID_27181882 Human_Splice_Rec_44403,Human_Splice_Rec_44425,Human_Splice_Rec_44457,Human_Splice_Rec_44461,Human_Splice_Rec_44477 RMVar_hsa_circ_65812,RMVar_hsa_circ_106077,RMVar_hsa_circ_114354,RMVar_hsa_circ_131325,RMVar_hsa_circ_131326,RMVar_hsa_circ_131327,RMVar_hsa_circ_23762,RMVar_hsa_circ_292133 88238 RMVar_ID_88238 Human_SNP_ID_8690706 m1A Human chr1 + 33013341 33013341 33013341 TGAGTGGGGTGGTTTGAGTGTGGTAGGCTTGCAGGCGGATTTTCAAGGCCTTTTCATTATCATCT TGAGTGGGGTGGTTTGAGTGTGGTAGGCTTGCCGGCGGATTTTCAAGGCCTTTTCATTATCATCT A C AL020995.1 Ensembl:ENSG00000236065 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:33013244..33013407 26863410 MeRIP-seq:(Medium) rs751151897 Functional Loss SNV dbSNP153 33..33 33 - - - 88239 RMVar_ID_88239 Human_SNP_ID_8690985 m1A Human chr1 - 33014550 33014550 33014550 CAAGAGTGGCCGTTCCTACCACGAGGAGTTCAACCCTCCAAAAGAGCCCATGAAAGATGACGTAT CAAGAGTGGCCGTTCCTACCACGAGGAGTTCAGCCCTCCAAAAGAGCCCATGAAAGATGACGTAT T C AK2 Ensembl:ENSG00000004455 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs371672441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3935706,Human_RBP_ID_18967935 Human_Splice_Rec_44400,Human_Splice_Rec_44401,Human_Splice_Rec_44412,Human_Splice_Rec_44413,Human_Splice_Rec_44422,Human_Splice_Rec_44423,Human_Splice_Rec_44432,Human_Splice_Rec_44433,Human_Splice_Rec_44442,Human_Splice_Rec_44443,Human_Splice_Rec_44454,Human_Splice_Rec_44455,Human_Splice_Rec_44474,Human_Splice_Rec_44475,Human_Splice_Rec_44486,Human_Splice_Rec_44487,Human_Splice_Rec_44498,Human_Splice_Rec_44499,Human_Splice_Rec_44504,Human_Splice_Rec_44506 Human_miRNA_ID_2293298,Human_miRNA_ID_2293299 RMVar_hsa_circ_106077,RMVar_hsa_circ_114354,RMVar_hsa_circ_131325,RMVar_hsa_circ_131326,RMVar_hsa_circ_131327,RMVar_hsa_circ_292133,RMVar_hsa_circ_131328,RMVar_hsa_circ_108939 88240 RMVar_ID_88240 Human_SNP_ID_8693470 m1A Human chr1 - 33024569 33024569 33024569 AATTGAATCTTGGTTTTTGTCTTCCTCTCTGTAGGCACCCAGATTGGCTGAAAACTTCTGTGTCT AATTGAATCTTGGTTTTTGTCTTCCTCTCTGTGGGCACCCAGATTGGCTGAAAACTTCTGTGTCT T C AK2 Ensembl:ENSG00000004455 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr1:33024555..33024629;chr1:33024526..33024575 26863196,32194978 MeRIP-seq:(Medium) rs749983131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851399,Human_RBP_ID_10950104,Human_RBP_ID_22562829,Human_RBP_ID_22633378,Human_RBP_ID_24687154 RMVar_hsa_circ_114354,RMVar_hsa_circ_131326,RMVar_hsa_circ_33935,RMVar_hsa_circ_309607 88241 RMVar_ID_88241 Human_SNP_ID_8696378 m1A Human chr1 - 33036647 33036647 33036647 GCCGGAGATCTAGAAGCCCTGGACCTGCCCGGAGCGGGCCGGGGACTAAGGCCTGCGGGGAACGC GCCGGAGATCTAGAAGCCCTGGACCTGCCCGGGGCGGGCCGGGGACTAAGGCCTGCGGGGAACGC T C AK2 Ensembl:ENSG00000004455 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:33036640..33036863 26863196 MeRIP-seq:(Medium) rs917174310 Functional Loss SNV dbSNP153 33..33 33 - - - 88242 RMVar_ID_88242 Human_SNP_ID_8696414 m1A Human chr1 - 33036732 33036732 33036732 GGCCTCCCGGGGCCGGTAAAGGGACCCAGGTGAGCGGCAGGACTGGGCTTGGCGGCGGAGCCTGC GGCCTCCCGGGGCCGGTAAAGGGACCCAGGTGGGCGGCAGGACTGGGCTTGGCGGCGGAGCCTGC T C AK2 Ensembl:ENSG00000004455 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:33036726..33036825 32194978 MeRIP-seq:(Medium) rs1168488476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801729,Human_RBP_ID_4075389,Human_RBP_ID_19037594 88243 RMVar_ID_88243 Human_SNP_ID_8696439 m1A Human chr1 + 33036767 33036767 33036767 CCTGGGTCCCTTTACCGGCCCCGGGAGGCCCCAGCAGCACGGCCCGGATGCCTTTAGGATACTCG CCTGGGTCCCTTTACCGGCCCCGGGAGGCCCCGGCAGCACGGCCCGGATGCCTTTAGGATACTCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:33036726..33036850 26863410 MeRIP-seq:(Medium) rs915278688 Functional Loss SNV dbSNP153 33..33 33 - - - 88244 RMVar_ID_88244 Human_SNP_ID_8696456 m1A Human chr1 + 33036793 33036793 33036793 GGCCCCAGCAGCACGGCCCGGATGCCTTTAGGATACTCGGGTTCTGCCGCTGGCACGCTGGGAGC GGCCCCAGCAGCACGGCCCGGATGCCTTTAGGGTACTCGGGTTCTGCCGCTGGCACGCTGGGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:33031658..33036981;chr1:33036359..33036964 26863196 MeRIP-seq:(Medium) rs750782742 Functional Loss SNV dbSNP153 33..33 33 - - - 88245 RMVar_ID_88245 Human_SNP_ID_8704742 m1A Human chr1 + 33070732 33070728 33070732 GCAGCAAGAAGAAGAAGAGGAGGAAGAAGAGAAAGAAGAAGAAGAGGAAGAAGAGGAAGAGGAGG GCAGCAAGAAGAAGAAGAGGAGGAAGAAG____AGAAGAAGAAGAGGAAGAAGAGGAAGAGGAGG GAGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33070705..33070780 26863196 MeRIP-seq:(Medium) rs1017637025 Functional Loss DEL dbSNP153 30..33 33 - - - 88246 RMVar_ID_88246 Human_SNP_ID_8715758 m1A Human chr1 - 33119300 33119300 33119300 TCCAAAAAACAAATCCCTGCCCTTGAGCTGCCAGCCATTTCCCTCTGCTCTCAGGCCCTGCAAGA TCCAAAAAACAAATCCCTGCCCTTGAGCTGCCGGCCATTTCCCTCTGCTCTCAGGCCCTGCAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33119252..33119389 26863196 MeRIP-seq:(Medium) rs1356612171 Functional Loss SNV dbSNP153 33..33 33 - - - 88247 RMVar_ID_88247 Human_SNP_ID_8724112 m1A Human chr1 - 33156979 33156979 33156979 AATGGGTTAGGAGACCACTGCATAATCCAGGCAAGAGGTGATGTGGGCGTGAAGCAGGGTGGTGG AATGGGTTAGGAGACCACTGCATAATCCAGGCCAGAGGTGATGTGGGCGTGAAGCAGGGTGGTGG T G TRIM62 Ensembl:ENSG00000116525 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33156976..33157207 26863196 MeRIP-seq:(Medium) rs1553170191 Functional Loss SNV dbSNP153 33..33 33 - - - 88248 RMVar_ID_88248 Human_SNP_ID_8724134 m1A Human chr1 + 33157068 33157068 33157068 TTCGGTCTATTCTCAACCCACTAGCCAAAGGGATCCTTAAAAAACTTAAACCAGTTCACGTCACT TTCGGTCTATTCTCAACCCACTAGCCAAAGGGTTCCTTAAAAAACTTAAACCAGTTCACGTCACT A T lnc-AZIN2-3 RNACentral:URS00009BDEF1 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:33157020..33157149 26863196 MeRIP-seq:(Medium) rs1453145991 Functional Loss SNV dbSNP153 33..33 33 - - - 88249 RMVar_ID_88249 Human_SNP_ID_8729673 m1A Human chr1 + 33180655 33180655 33180655 CCTCAGTCTGACAGTGGCCCTGCCTTTGCCCAACTCTGATTCCGGTTCGTCCACAACCCTGCCCC CCTCAGTCTGACAGTGGCCCTGCCTTTGCCCAGCTCTGATTCCGGTTCGTCCACAACCCTGCCCC A G lnc-AZIN2-3 RNACentral:URS00009BDEF1 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33180373..33180711 26863196 MeRIP-seq:(Medium) rs183140678 Functional Loss SNV dbSNP153 33..33 33 - - - 88250 RMVar_ID_88250 Human_SNP_ID_8730050 m1A Human chr1 - 33181577 33181577 33181577 CCCTTCCTCGCGTTACCCTCCTTCCGGACAGCACCCCCTCCCTTCTCCGGTAGCTCCTACCCCTG CCCTTCCTCGCGTTACCCTCCTTCCGGACAGCGCCCCCTCCCTTCTCCGGTAGCTCCTACCCCTG T C TRIM62 Ensembl:ENSG00000116525 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:33181450..33181594 26863196 MeRIP-seq:(Medium) rs1274766644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125694 88251 RMVar_ID_88251 Human_SNP_ID_8747687 m1A Human chr1 + 33256537 33256537 33256537 AGGCGACCCGGAAGGTTTGCGCGCGGCTCCGCAGCGAGCCAGAGCCGGAGCCCGAGCCCGGAGCC AGGCGACCCGGAAGGTTTGCGCGCGGCTCCGCGGCGAGCCAGAGCCGGAGCCCGAGCCCGGAGCC A G ZNF362 Ensembl:ENSG00000160094 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:33256330..33256973 26863196 MeRIP-seq:(Medium) rs1204253895 Functional Loss SNV dbSNP153 33..33 33 - - - 88252 RMVar_ID_88252 Human_SNP_ID_8747839 m1A Human chr1 - 33256863 33256863 33256863 CAGCCCCAGACACGCCGCGGGAGACACTTCCTACCCCGCGCGCCCCGCTGCCGCCGCCGCCGCCG CAGCCCCAGACACGCCGCGGGAGACACTTCCTCCCCCGCGCGCCCCGCTGCCGCCGCCGCCGCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:33256814..33256955 26863196 MeRIP-seq:(Medium) rs957168812 Functional Loss SNV dbSNP153 33..33 33 - - - 88253 RMVar_ID_88253 Human_SNP_ID_8752739 m1A Human chr1 + 33277566 33277565 33277566 GAGTCTGGCTGCTAGGTGGAGACCCGGTTGTCAGGGGGTAAGCATGGAAGCAGGGAGACCTTCAG GAGTCTGGCTGCTAGGTGGAGACCCGGTTGTC_GGGGGTAAGCATGGAAGCAGGGAGACCTTCAG CA C ZNF362 Ensembl:ENSG00000160094 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33277564..33277766 26863196 MeRIP-seq:(Medium) rs1233452329 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_66022,RMVar_hsa_circ_123326,RMVar_hsa_circ_131335,RMVar_hsa_circ_306184,RMVar_hsa_circ_125296,RMVar_hsa_circ_131341,RMVar_hsa_circ_131338,RMVar_hsa_circ_131339,RMVar_hsa_circ_307295,RMVar_hsa_circ_349056,RMVar_hsa_circ_327414 88254 RMVar_ID_88254 Human_SNP_ID_8753340 m1A Human chr1 + 33280232 33280227 33280233 CAGCACCCCGTCCACACCCACCACCACCAGCCAGAGCCGCCTCATCGCCTCGTCCCCCACCCTCA CAGCACCCCGTCCACACCCACCACCACC______AGCCGCCTCATCGCCTCGTCCCCCACCCTCA CAGCCAG C ZNF362 Ensembl:ENSG00000160094 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:33280182..33280294 26863196 MeRIP-seq:(Medium) rs759348133 Functional Loss DEL dbSNP153 29..34 33 - - - Human_miRNA_ID_792716,Human_miRNA_ID_2329894,Human_miRNA_ID_2962971,Human_miRNA_ID_3067721 RMVar_hsa_circ_66022,RMVar_hsa_circ_123326,RMVar_hsa_circ_131335,RMVar_hsa_circ_306184,RMVar_hsa_circ_125296,RMVar_hsa_circ_131341,RMVar_hsa_circ_131338,RMVar_hsa_circ_131339,RMVar_hsa_circ_307295,RMVar_hsa_circ_349056,RMVar_hsa_circ_327414,RMVar_hsa_circ_131343,RMVar_hsa_circ_290095,RMVar_hsa_circ_277079,RMVar_hsa_circ_131342 88255 RMVar_ID_88255 Human_SNP_ID_8757983 m1A Human chr1 + 33299553 33299553 33299553 GCCTAGGTTTCTGGACTGCAAAGGGGACCCCCAGGTGGGAGGGGCAGGAAGCAGCCGGAGTGAGC GCCTAGGTTTCTGGACTGCAAAGGGGACCCCCGGGTGGGAGGGGCAGGAAGCAGCCGGAGTGAGC A G ZNF362 Ensembl:ENSG00000160094 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33299503..33299694 26863196 MeRIP-seq:(Medium) rs1420120300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334205,Human_RBP_ID_5137472,Human_RBP_ID_5518772,Human_RBP_ID_8171304,Human_RBP_ID_17456800,Human_RBP_ID_18157761,Human_RBP_ID_21959397,Human_RBP_ID_21963609 RMVar_hsa_circ_76779,RMVar_hsa_circ_131347 88256 RMVar_ID_88256 Human_SNP_ID_8765013 m1A Human chr1 - 33324119 33324119 33324119 TAGCCAAGAATGGCAGCCTCAGCGCAGAGGCAAGGTCAGAAAGAGACGGCGCTTCAGAGTTTCCT TAGCCAAGAATGGCAGCCTCAGCGCAGAGGCACGGTCAGAAAGAGACGGCGCTTCAGAGTTTCCT T G PHC2 Ensembl:ENSG00000134686 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:33323726..33324125 32194978 MeRIP-seq:(Medium) rs956059312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353234,Human_RBP_ID_17749314,Human_RBP_ID_23389630 Human_miRNA_ID_467451,Human_miRNA_ID_605609 88257 RMVar_ID_88257 Human_SNP_ID_8767632 m1A Human chr1 - 33334223 33334223 33334223 CAGCAGCCCCGGCATGACCTCAGGGAACGGAAACTCTGCCTCCAGCATCGCCGGCACTGCCCCCC CAGCAGCCCCGGCATGACCTCAGGGAACGGAACCTCTGCCTCCAGCATCGCCGGCACTGCCCCCC T G PHC2 Ensembl:ENSG00000134686 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:33331665..33334284 32194978 MeRIP-seq:(Medium) rs1254561651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073836,Human_RBP_ID_24748121,Human_RBP_ID_26863108 Human_Splice_Rec_44872,Human_Splice_Rec_44884,Human_Splice_Rec_44885,Human_Splice_Rec_44898,Human_Splice_Rec_44912,Human_Splice_Rec_44938,Human_Splice_Rec_44950,Human_Splice_Rec_44951,Human_Splice_Rec_44964,Human_Splice_Rec_44965,Human_Splice_Rec_44972,Human_Splice_Rec_44973 Human_miRNA_ID_2473912,Human_miRNA_ID_2473913,Human_miRNA_ID_2959698,Human_miRNA_ID_2959699 RMVar_hsa_circ_84923,RMVar_hsa_circ_112262,RMVar_hsa_circ_333451,RMVar_hsa_circ_101829,RMVar_hsa_circ_131350,RMVar_hsa_circ_75636,RMVar_hsa_circ_84610,RMVar_hsa_circ_131352,RMVar_hsa_circ_131353,RMVar_hsa_circ_131351,RMVar_hsa_circ_94992,RMVar_hsa_circ_131349,RMVar_hsa_circ_131355 88258 RMVar_ID_88258 Human_SNP_ID_8771312 m1A Human chr1 - 33349634 33349634 33349634 GCGCGAGTCGGCGCCCGGCCGAGGGGCTGCGTAGGCCCCGCCCGGCCAGGCCCAGCCGGGCCCTG GCGCGAGTCGGCGCCCGGCCGAGGGGCTGCGTGGGCCCCGCCCGGCCAGGCCCAGCCGGGCCCTG T C PHC2 Ensembl:ENSG00000134686 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:33349596..33349696 32194978 MeRIP-seq:(Medium) rs1390961937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4046894,Human_RBP_ID_18455593,Human_RBP_ID_26773372 Human_Splice_Rec_44883,Human_Splice_Rec_44897,Human_Splice_Rec_44949,Human_Splice_Rec_44963,Human_Splice_Rec_44971 RMVar_hsa_circ_84923,RMVar_hsa_circ_101829,RMVar_hsa_circ_131350,RMVar_hsa_circ_75636,RMVar_hsa_circ_84610,RMVar_hsa_circ_131352,RMVar_hsa_circ_131351,RMVar_hsa_circ_94992,RMVar_hsa_circ_131349,RMVar_hsa_circ_131355 88259 RMVar_ID_88259 Human_SNP_ID_8771404 m1A Human chr1 + 33349824 33349824 33349824 AGGCCGGGACGGGGGCGCGAGGCCGGGGCGGGAGCGCGGGCGGCGGCCGGGGTTGCGCGCGCGCG AGGCCGGGACGGGGGCGCGAGGCCGGGGCGGGGGCGCGGGCGGCGGCCGGGGTTGCGCGCGCGCG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:33349701..33349900 26863410 MeRIP-seq:(Medium) rs1234322034 Functional Loss SNV dbSNP153 33..33 33 - - - 88260 RMVar_ID_88260 Human_SNP_ID_8771434 m1A Human chr1 - 33349869 33349869 33349869 CCGCATTGTCTCCGCGGCGGCTGCAGCCCTCGAGCGCCCGCCGCGCGCGCGCGCGCAACCCCGGC CCGCATTGTCTCCGCGGCGGCTGCAGCCCTCGGGCGCCCGCCGCGCGCGCGCGCGCAACCCCGGC T C PHC2 Ensembl:ENSG00000134686 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:33349695..33349885 26863410 MeRIP-seq:(Medium) rs1439628054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801838,Human_RBP_ID_4072690 RMVar_hsa_circ_84923,RMVar_hsa_circ_101829,RMVar_hsa_circ_131350,RMVar_hsa_circ_75636,RMVar_hsa_circ_84610,RMVar_hsa_circ_131352,RMVar_hsa_circ_131351,RMVar_hsa_circ_94992,RMVar_hsa_circ_131349,RMVar_hsa_circ_131355 88261 RMVar_ID_88261 Human_SNP_ID_9164641 m1A Human chr1 + 34983896 34983896 34983896 AGCTATTTGGTAGTTCAGGGGATCTGGCTGGTAGCCAAATACCTTCAGCGGGAACACCTCAGCAA AGCTATTTGGTAGTTCAGGGGATCTGGCTGGTGGCCAAATACCTTCAGCGGGAACACCTCAGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:34983847..34985305 26863196 MeRIP-seq:(Medium) rs1331220681 Functional Loss SNV dbSNP153 33..33 33 - - - 88262 RMVar_ID_88262 Human_SNP_ID_9176588 m1A Human chr1 - 35031830 35031830 35031830 CTTGGTTCCTATTCCAGTGCTCCTCCGGTAGCAGGGAGGCGACAGAAGGTGGGTGCGGCCGCAGT CTTGGTTCCTATTCCAGTGCTCCTCCGGTAGCGGGGAGGCGACAGAAGGTGGGTGCGGCCGCAGT T C ZMYM6 Ensembl:ENSG00000163867 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:35031823..35031905 26863410 MeRIP-seq:(Medium) rs1331369717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_46043,Human_Splice_Rec_46093,Human_Splice_Rec_46099,Human_Splice_Rec_46109 88263 RMVar_ID_88263 Human_SNP_ID_9176595 m1A Human chr1 + 35031845 35031845 35031845 ACCTTCTGTCGCCTCCCTGCTACCGGAGGAGCACTGGAATAGGAACCAAGTCCTCTGCATCTAGA ACCTTCTGTCGCCTCCCTGCTACCGGAGGAGCTCTGGAATAGGAACCAAGTCCTCTGCATCTAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35031814..35031907 26863196 MeRIP-seq:(Medium) rs541109275 Functional Loss SNV dbSNP153 33..33 33 - - - 88264 RMVar_ID_88264 Human_SNP_ID_9213764 m1A Human chr1 - 35178383 35178383 35178383 ATGTGCTTTCATATGAAAAAAGAGCTGATGTTAAAACTCATTTGGTGAGGTCAACGTTGTCACAT ATGTGCTTTCATATGAAAAAAGAGCTGATGTTGAAACTCATTTGGTGAGGTCAACGTTGTCACAT T C SFPQ Ensembl:ENSG00000116560 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:35178285..35178436 32194978 MeRIP-seq:(Medium) rs927204068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272792,Human_RBP_ID_353437,Human_RBP_ID_1429976,Human_RBP_ID_1746130,Human_RBP_ID_9516310,Human_RBP_ID_10954342,Human_RBP_ID_22862481,Human_RBP_ID_24688017,Human_RBP_ID_26587211,Human_RBP_ID_27593685 RMVar_hsa_circ_80884,RMVar_hsa_circ_131442,RMVar_hsa_circ_73151,RMVar_hsa_circ_300760,RMVar_hsa_circ_131443 88265 RMVar_ID_88265 Human_SNP_ID_9216626 m1A Human chr1 + 35187956 35187955 35187956 GCAAGTTCTATAGACAACTCCAATTGGAAGGCAGTAAAGGCTGACTTACTGGATCCATGTAGCCC GCAAGTTCTATAGACAACTCCAATTGGAAGGC_GTAAAGGCTGACTTACTGGATCCATGTAGCCC CA C RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:35187951..35188025 26863196 MeRIP-seq:(Medium) rs1274212811 Functional Loss DEL dbSNP153 33..33 33 - - - 88266 RMVar_ID_88266 Human_SNP_ID_9217006 m1A Human chr1 - 35189023 35189023 35189023 ATGGAAGAACTTCACAATCAAGAAATGCAGAAACGTAAAGAAATGCAATTGAGGTAAAATTGTGT ATGGAAGAACTTCACAATCAAGAAATGCAGAAGCGTAAAGAAATGCAATTGAGGTAAAATTGTGT T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35189001..35189075 26863196 MeRIP-seq:(Medium) rs1452923897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221380,Human_RBP_ID_353555,Human_RBP_ID_859586,Human_RBP_ID_1123142,Human_RBP_ID_1430176,Human_RBP_ID_1746246,Human_RBP_ID_2144727,Human_RBP_ID_3311105,Human_RBP_ID_5544949,Human_RBP_ID_5815405,Human_RBP_ID_8240785,Human_RBP_ID_9355986,Human_RBP_ID_17061818,Human_RBP_ID_17452643,Human_RBP_ID_18430215,Human_RBP_ID_18524720,Human_RBP_ID_18573048,Human_RBP_ID_22784723,Human_RBP_ID_23390491,Human_RBP_ID_24541068,Human_RBP_ID_24688476,Human_RBP_ID_26310794,Human_RBP_ID_26863436,Human_RBP_ID_27398084,Human_RBP_ID_27797772 Human_Splice_Rec_46298,Human_Splice_Rec_46299,Human_Splice_Rec_46344,Human_Splice_Rec_46345 RMVar_hsa_circ_131444,RMVar_hsa_circ_73151,RMVar_hsa_circ_106327,RMVar_hsa_circ_88156,RMVar_hsa_circ_131446,RMVar_hsa_circ_77616,RMVar_hsa_circ_131445,RMVar_hsa_circ_26727,RMVar_hsa_circ_58989,RMVar_hsa_circ_63278,RMVar_hsa_circ_69466,RMVar_hsa_circ_318687,RMVar_hsa_circ_361736 88267 RMVar_ID_88267 Human_SNP_ID_9217091 m1A Human chr1 - 35189251 35189251 35189251 GGAACAAGTTGAAAAAAACATGAAAGATGCAAAAGACAAATTGGAAAGTGAAATGGAAGATGCCT GGAACAAGTTGAAAAAAACATGAAAGATGCAAGAGACAAATTGGAAAGTGAAATGGAAGATGCCT T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:35189105..35189308 26863196 MeRIP-seq:(Medium) rs1318099605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1430181,Human_RBP_ID_1746248,Human_RBP_ID_5815410,Human_RBP_ID_9355989,Human_RBP_ID_10955078,Human_RBP_ID_17452645,Human_RBP_ID_17749629,Human_RBP_ID_18523194,Human_RBP_ID_18573049,Human_RBP_ID_23390496,Human_RBP_ID_26310800,Human_RBP_ID_26863440 Human_Splice_Rec_46297,Human_Splice_Rec_46343 RMVar_hsa_circ_131444,RMVar_hsa_circ_73151,RMVar_hsa_circ_106327,RMVar_hsa_circ_88156,RMVar_hsa_circ_131446,RMVar_hsa_circ_77616,RMVar_hsa_circ_131445,RMVar_hsa_circ_58989,RMVar_hsa_circ_11321,RMVar_hsa_circ_63278,RMVar_hsa_circ_318687,RMVar_hsa_circ_361736 88268 RMVar_ID_88268 Human_SNP_ID_9218240 m1A Human chr1 - 35192244 35192244 35192244 GCCCCCGCCCGGCGGGCCCGGCGGCCGCAGCGAGGAGAAGATCTCGGACTCGGAGGTGAGTGTCT GCCCCCGCCCGGCGGGCCCGGCGGCCGCAGCGGGGAGAAGATCTCGGACTCGGAGGTGAGTGTCT T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:35192220..35192432;chr1:35192214..35192418 26863196 MeRIP-seq:(Medium) rs1198525045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221383,Human_RBP_ID_803359,Human_RBP_ID_859595,Human_RBP_ID_5335218,Human_RBP_ID_9358595,Human_RBP_ID_10955216,Human_RBP_ID_19037614,Human_RBP_ID_22429231,Human_RBP_ID_26863467 Human_Splice_Rec_46335 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 88269 RMVar_ID_88269 Human_SNP_ID_9218244 m1A Human chr1 - 35192248 35192248 35192248 AGGGGCCCCCGCCCGGCGGGCCCGGCGGCCGCAGCGAGGAGAAGATCTCGGACTCGGAGGTGAGT AGGGGCCCCCGCCCGGCGGGCCCGGCGGCCGCGGCGAGGAGAAGATCTCGGACTCGGAGGTGAGT T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:35192219..35192435 26863196 MeRIP-seq:(Medium) rs932770892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221383,Human_RBP_ID_803359,Human_RBP_ID_859595,Human_RBP_ID_4047425,Human_RBP_ID_5335218,Human_RBP_ID_9358595,Human_RBP_ID_10955216,Human_RBP_ID_19037614,Human_RBP_ID_22429231,Human_RBP_ID_26863467 Human_Splice_Rec_46335 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 88270 RMVar_ID_88270 Human_SNP_ID_9218434 m1A Human chr1 - 35192621 35192621 35192621 CCCGCCACTCCACCAACCTCGGGGGCCCCGCCAGGGTCCGGGCCAGGCCCGACTCCGACCCCGCC CCCGCCACTCCACCAACCTCGGGGGCCCCGCCGGGGTCCGGGCCAGGCCCGACTCCGACCCCGCC T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:35192533..35192815 26863196 MeRIP-seq:(Medium) rs1013504901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18241,Human_RBP_ID_273325,Human_RBP_ID_803360,Human_RBP_ID_22531945 Human_miRNA_ID_2145894,Human_miRNA_ID_2987329,Human_miRNA_ID_3021019 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 88271 RMVar_ID_88271 Human_SNP_ID_9218492 m1A Human chr1 - 35192727 35192727 35192727 GCAGCCGCCGCCACCGCCGCAGGACTCTTCCAAGCCCGTCGTTGCTCAGGGACCCGGCCCCGCTC GCAGCCGCCGCCACCGCCGCAGGACTCTTCCAGGCCCGTCGTTGCTCAGGGACCCGGCCCCGCTC T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:35192501..35193150 26863196 MeRIP-seq:(Medium) rs1283378510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803361,Human_RBP_ID_1430212,Human_RBP_ID_1746263,Human_RBP_ID_4047457,Human_RBP_ID_5815456,Human_RBP_ID_8240789,Human_RBP_ID_8309427,Human_RBP_ID_10955218,Human_RBP_ID_17218212,Human_RBP_ID_17452653,Human_RBP_ID_17677686,Human_RBP_ID_18573096,Human_RBP_ID_22531946,Human_RBP_ID_26863476,Human_RBP_ID_27398103 Human_miRNA_ID_1972019,Human_miRNA_ID_1974196 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 88272 RMVar_ID_88272 Human_SNP_ID_9218676 m1A Human chr1 + 35192967 35192967 35192967 CCATGCCGGGCGGCGGAGAACGGAAGTCGTGGAGGCCGCCGCGGCCGCCGCCTCCTCCACGCCTG CCATGCCGGGCGGCGGAGAACGGAAGTCGTGGGGGCCGCCGCGGCCGCCGCCTCCTCCACGCCTG A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:35192951..35192975 26863196 MeRIP-seq:(Medium) rs1557821107 Functional Loss SNV dbSNP153 33..33 33 - - - 88273 RMVar_ID_88273 Human_SNP_ID_9218730 m1A Human chr1 + 35193086 35193086 35193086 GTGGTCAAGGGGCGGTCGAGGCAAAAGCGAAGAAGACGCTCAGGAAACGTGGAGGCCACCTTGCT GTGGTCAAGGGGCGGTCGAGGCAAAAGCGAAGCAGACGCTCAGGAAACGTGGAGGCCACCTTGCT A C RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:35192522..35193150;chr1:35192499..35193150;chr1:35192501..35193150 26863196 MeRIP-seq:(Medium) rs1224657604 Functional Loss SNV dbSNP153 33..33 33 - - - 88274 RMVar_ID_88274 Human_SNP_ID_9218753 m1A Human chr1 - 35193114 35193114 35193114 CGCCTGTGTCATCCGCCATTTTGTGAGAAGCAAGGTGGCCTCCACGTTTCCTGAGCGTCTTCTTC CGCCTGTGTCATCCGCCATTTTGTGAGAAGCAGGGTGGCCTCCACGTTTCCTGAGCGTCTTCTTC T C SFPQ Ensembl:ENSG00000116560 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:35193076..35193150 26863196 MeRIP-seq:(Medium) rs559709445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353571,Human_RBP_ID_741973,Human_RBP_ID_1255370,Human_RBP_ID_1430219,Human_RBP_ID_1746267,Human_RBP_ID_4047468,Human_RBP_ID_5815463,Human_RBP_ID_8309435,Human_RBP_ID_9356016,Human_RBP_ID_17218217,Human_RBP_ID_18573107,Human_RBP_ID_22020612,Human_RBP_ID_22142439,Human_RBP_ID_23390517,Human_RBP_ID_26310819,Human_RBP_ID_26863485,Human_RBP_ID_27398114,Human_RBP_ID_27800045 Human_miRNA_ID_2401785 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 88275 RMVar_ID_88275 Human_SNP_ID_9239296 m1A Human chr1 + 35269007 35269007 35269007 CGGGGGCCGGGGGGCCGAGAGGTACCGCCGCCACCGCGCGGGGAGCCGCAGCGGTTCCGAGCGGG CGGGGGCCGGGGGGCCGAGAGGTACCGCCGCCGCCGCGCGGGGAGCCGCAGCGGTTCCGAGCGGG A G ZMYM4 Ensembl:ENSG00000146463 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35268957..35269259 26863196 MeRIP-seq:(Medium) rs1465863392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224207,Human_RBP_ID_5312451,Human_RBP_ID_8228262,Human_RBP_ID_8753833 Human_Splice_Rec_46353,Human_Splice_Rec_46411 88276 RMVar_ID_88276 Human_SNP_ID_9239302 m1A Human chr1 + 35269034 35269011 35269034 CCGCCACCGCGCGGGGAGCCGCAGCGGTTCCGAGCGGGGCCCAACATGGCGGAGAGAGAGGTGGA CCGCCACCGC_______________________GCGGGGCCCAACATGGCGGAGAGAGAGGTGGA CGCGGGGAGCCGCAGCGGTTCCGA C ZMYM4 Ensembl:ENSG00000146463 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35268984..35269256 26863196 MeRIP-seq:(Medium) rs1441884818 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_5312451,Human_RBP_ID_8228262,Human_RBP_ID_9271244 Human_Splice_Rec_46353,Human_Splice_Rec_46411 88277 RMVar_ID_88277 Human_SNP_ID_9281084 m1A Human chr1 + 35436864 35436864 35436864 ACTCCCGCGCACACACATCCTCTTTCCCCCCAACGGACCCACTCAGTTTACCCTTCTTCCAGCTA ACTCCCGCGCACACACATCCTCTTTCCCCCCAGCGGACCCACTCAGTTTACCCTTCTTCCAGCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:35436775..35436889 26863196 MeRIP-seq:(Medium) rs771604696 Functional Loss SNV dbSNP153 33..33 33 - - - 88278 RMVar_ID_88278 Human_SNP_ID_9296419 m1A Human chr1 - 35502569 35502569 35502569 AGCTGTGGAAGAGGGTTGCTGGGGTAGAGTGGAGAAGAAGTTTATTGGAGGCAAGGAGCTCAAAG AGCTGTGGAAGAGGGTTGCTGGGGTAGAGTGGCGAAGAAGTTTATTGGAGGCAAGGAGCTCAAAG T G KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35502480..35502752 26863196 MeRIP-seq:(Medium) rs1558504132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5816784,Human_RBP_ID_23390931,Human_RBP_ID_24690319 RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_35232,RMVar_hsa_circ_131526,RMVar_hsa_circ_324653,RMVar_hsa_circ_268206,RMVar_hsa_circ_348442,RMVar_hsa_circ_131530,RMVar_hsa_circ_303601 88279 RMVar_ID_88279 Human_SNP_ID_9296420 m1A Human chr1 - 35502574 35502574 35502574 GGGTGAGCTGTGGAAGAGGGTTGCTGGGGTAGAGTGGAGAAGAAGTTTATTGGAGGCAAGGAGCT GGGTGAGCTGTGGAAGAGGGTTGCTGGGGTAGGGTGGAGAAGAAGTTTATTGGAGGCAAGGAGCT T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35502554..35502816 26863196 MeRIP-seq:(Medium) rs560813453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5816784,Human_RBP_ID_23390931,Human_RBP_ID_24690319 RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_35232,RMVar_hsa_circ_131526,RMVar_hsa_circ_324653,RMVar_hsa_circ_268206,RMVar_hsa_circ_348442,RMVar_hsa_circ_131530,RMVar_hsa_circ_303601 88280 RMVar_ID_88280 Human_SNP_ID_9301489 m1A Human chr1 - 35523058 35523058 35523058 GTGTGATACAAGCTGGAGCTAGAAAGGTAGGTAGGGTCCAAACCATACAAGATTTTTTTTTTTTT GTGTGATACAAGCTGGAGCTAGAAAGGTAGGTGGGGTCCAAACCATACAAGATTTTTTTTTTTTT T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35523056..35523241 26863196 MeRIP-seq:(Medium) rs1053600579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 88281 RMVar_ID_88281 Human_SNP_ID_9308612 m1A Human chr1 - 35554521 35554521 35554521 CGGCATGTAATTTCTTCTCTTTCTGTCCTTCTAGTGTACTGGTTCTGCCTGTCTGGAGGGCCATG CGGCATGTAATTTCTTCTCTTTCTGTCCTTCTGGTGTACTGGTTCTGCCTGTCTGGAGGGCCATG T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35554475..35554553 26863196 MeRIP-seq:(Medium) rs1446510410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073849 RMVar_hsa_circ_268206,RMVar_hsa_circ_106598,RMVar_hsa_circ_131532 88282 RMVar_ID_88282 Human_SNP_ID_9309291 m1A Human chr1 - 35557359 35557359 35557359 CGTCGCTGTCCAGGGAGGCTGAGGCGAGAGGTAGCTGTCCGGGTGGGGAGCCCGCACTACCTTCT CGTCGCTGTCCAGGGAGGCTGAGGCGAGAGGTGGCTGTCCGGGTGGGGAGCCCGCACTACCTTCT T C KIAA0319L Ensembl:ENSG00000142687 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:35557231..35557379;chr1:35557213..35557374 26863196 MeRIP-seq:(Medium) rs548312231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072697,Human_RBP_ID_18414926,Human_RBP_ID_22558596,Human_RBP_ID_23122630 RMVar_hsa_circ_268206,RMVar_hsa_circ_106598,RMVar_hsa_circ_131532 88283 RMVar_ID_88283 Human_SNP_ID_9310403 m1A Human chr1 + 35561122 35561122 35561122 GGCGTGCGTGGAAGTGCGGCTGGCACTGGAGGAGACGGGCACGGAGGTGAAAGAGGATGTGGTGA GGCGTGCGTGGAAGTGCGGCTGGCACTGGAGGGGACGGGCACGGAGGTGAAAGAGGATGTGGTGA A G NCDN Ensembl:ENSG00000020129 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:35561075..35561190 26863196 MeRIP-seq:(Medium) rs1465160957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800905,Human_RBP_ID_18965212,Human_RBP_ID_22023177,Human_RBP_ID_23117648,Human_RBP_ID_23205100 Human_miRNA_ID_2014529,Human_miRNA_ID_2464519 RMVar_hsa_circ_110117,RMVar_hsa_circ_131533 88284 RMVar_ID_88284 Human_SNP_ID_9310418 m1A Human chr1 - 35561152 35561152 35561152 TCCCCAACTCCATGAGGGCATAGCAGGCGGTCACCACATCCTCTTTCACCTCCGTGCCCGTCTCC TCCCCAACTCCATGAGGGCATAGCAGGCGGTCGCCACATCCTCTTTCACCTCCGTGCCCGTCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35561101..35561213 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 88285 RMVar_ID_88285 Human_SNP_ID_9320018 m1A Human chr1 - 35600107 35600089 35600108 ACAGGGTCTTGCTCCATCACCTAGGCTGGAGTACAGTGGCACGATCGTAGCTTACTGCAGTAAGT ACAGGGTCTTGCTCCATCACCTAGGCTGGAG___________________CTTACTGCAGTAAGT GCTACGATCGTGCCACTGTA G PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1353487442 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_5817031,Human_RBP_ID_8167940,Human_RBP_ID_10960886,Human_RBP_ID_19349711,Human_RBP_ID_26379610 88286 RMVar_ID_88286 Human_SNP_ID_9320512 m1A Human chr1 - 35602183 35602183 35602183 GGATTACAGGCGCACACCACCAATGCCCAGCTAGTTTTTGTGTTTTTCATAGAGACAGGGTCTCA GGATTACAGGCGCACACCACCAATGCCCAGCTGGTTTTTGTGTTTTTCATAGAGACAGGGTCTCA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1132065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167941,Human_RBP_ID_26379655 88287 RMVar_ID_88287 Human_SNP_ID_9322199 m1A Human chr1 + 35609277 35609277 35609277 CTCGGTGTGTAGTATCGGTCGAGGATACTGAGAGTCAGGAAGGCACCATAGCCGTGGGCTGCAAA CTCGGTGTGTAGTATCGGTCGAGGATACTGAGTGTCAGGAAGGCACCATAGCCGTGGGCTGCAAA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:35609226..35609425 26863196 MeRIP-seq:(Medium) rs770469718 Functional Loss SNV dbSNP153 33..33 33 - - - 88288 RMVar_ID_88288 Human_SNP_ID_9348829 m1A Human chr1 + 35719092 35719092 35719092 TCGCTGCAGACACCGTGCCATTTTCAAGTGAAATCTGATTAGTCACCACCTTCCGGCGTTAAACT TCGCTGCAGACACCGTGCCATTTTCAAGTGAATTCTGATTAGTCACCACCTTCCGGCGTTAAACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35719043..35719370 26863196 MeRIP-seq:(Medium) rs1458562294 Functional Loss SNV dbSNP153 33..33 33 - - - 88289 RMVar_ID_88289 Human_SNP_ID_9348881 m1A Human chr1 + 35719237 35719236 35719238 CTCCGGCTTCGTCCTCTACCCTCCCTCTCCGCAGTTACCCTCCCACACGCCCCTTTCCGCCACGC CTCCGGCTTCGTCCTCTACCCTCCCTCTCCGC__TTACCCTCCCACACGCCCCTTTCCGCCACGC CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:35719187..35719336 26863196 MeRIP-seq:(Medium) rs1164546426 Functional Loss DEL dbSNP153 33..34 33 - - - 88290 RMVar_ID_88290 Human_SNP_ID_9353245 m1A Human chr1 - 35738099 35738099 35738099 ATATATATATATATATATTTTTTTTTTTTTTCAGGCACAGCAGGGGAAAATTACAGCTGAAGAAG ATATATATATATATATATTTTTTTTTTTTTTCTGGCACAGCAGGGGAAAATTACAGCTGAAGAAG T A CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35738050..35738507 26863196 MeRIP-seq:(Medium) rs768307795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11882,RMVar_hsa_circ_106242,RMVar_hsa_circ_131544,RMVar_hsa_circ_376233,RMVar_hsa_circ_16643,RMVar_hsa_circ_131545 88291 RMVar_ID_88291 Human_SNP_ID_9353246 m1A Human chr1 - 35738099 35738099 35738099 ATATATATATATATATATTTTTTTTTTTTTTCAGGCACAGCAGGGGAAAATTACAGCTGAAGAAG ATATATATATATATATATTTTTTTTTTTTTTCGGGCACAGCAGGGGAAAATTACAGCTGAAGAAG T C CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35738050..35738507 26863196 MeRIP-seq:(Medium) rs768307795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11882,RMVar_hsa_circ_106242,RMVar_hsa_circ_131544,RMVar_hsa_circ_376233,RMVar_hsa_circ_16643,RMVar_hsa_circ_131545 88292 RMVar_ID_88292 Human_SNP_ID_9353247 m1A Human chr1 - 35738099 35738099 35738099 ATATATATATATATATATTTTTTTTTTTTTTCAGGCACAGCAGGGGAAAATTACAGCTGAAGAAG ATATATATATATATATATTTTTTTTTTTTTTCCGGCACAGCAGGGGAAAATTACAGCTGAAGAAG T G CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35738050..35738507 26863196 MeRIP-seq:(Medium) rs768307795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11882,RMVar_hsa_circ_106242,RMVar_hsa_circ_131544,RMVar_hsa_circ_376233,RMVar_hsa_circ_16643,RMVar_hsa_circ_131545 88293 RMVar_ID_88293 Human_SNP_ID_9356594 m1A Human chr1 - 35751337 35751329 35751338 GAAATGACAGATGAGTCTGAGGAAGATGGAGAAGAGAAGGTAGAGAAAGAAGAGAAAGAGGAAGA GAAATGACAGATGAGTCTGAGGAAGATGGAG_________TAGAGAAAGAAGAGAAAGAGGAAGA ACCTTCTCTT A CLSPN Ensembl:ENSG00000092853 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:35751206..35751450;chr1:35749749..35751475;chr1:35749751..35751488 26863196 MeRIP-seq:(Medium) rs1557514067 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_849820,Human_RBP_ID_1438132,Human_RBP_ID_4048113,Human_RBP_ID_5817428,Human_RBP_ID_9443799,Human_RBP_ID_22870821,Human_RBP_ID_23391303,Human_RBP_ID_24541078,Human_RBP_ID_24550348,Human_RBP_ID_26310832 Human_Splice_Rec_46849,Human_Splice_Rec_46895,Human_Splice_Rec_46945,Human_Splice_Rec_46991 RMVar_hsa_circ_376233,RMVar_hsa_circ_16643,RMVar_hsa_circ_33080,RMVar_hsa_circ_47687,RMVar_hsa_circ_81601,RMVar_hsa_circ_131545,RMVar_hsa_circ_131548,RMVar_hsa_circ_305443,RMVar_hsa_circ_360512,RMVar_hsa_circ_110581,RMVar_hsa_circ_266849,RMVar_hsa_circ_131555 88294 RMVar_ID_88294 Human_SNP_ID_9361154 m1A Human chr1 - 35770200 35770200 35770200 GATGCTTTGGCAAGTGTCAAAGGTCAAAGACCACGGCTCGCCTGGTACCGACTGCCCCGCCCCCG GATGCTTTGGCAAGTGTCAAAGGTCAAAGACCGCGGCTCGCCTGGTACCGACTGCCCCGCCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35770149..35770214 26863196 MeRIP-seq:(Medium) rs1284992982 Functional Loss SNV dbSNP153 33..33 33 - - - 88295 RMVar_ID_88295 Human_SNP_ID_9369438 m1A Human chr1 - 35806748 35806748 35806748 GTGTCCAAATTTCCTCTTCTTATAAGGACAGCAGTCCTATTAGAGTAGGGCTCACTCTAGTGACC GTGTCCAAATTTCCTCTTCTTATAAGGACAGCTGTCCTATTAGAGTAGGGCTCACTCTAGTGACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35806738..35806896 26863196 MeRIP-seq:(Medium) rs1000974865 Functional Loss SNV dbSNP153 33..33 33 - - - 88296 RMVar_ID_88296 Human_SNP_ID_9369793 m1A Human chr1 - 35808047 35808047 35808047 GGCGTGCGCGGCCCCGGGCGCGGGGTCCACAGAGCCCGGCAGGCGGCGAGGCGGGTCGGGGAACG GGCGTGCGCGGCCCCGGGCGCGGGGTCCACAGGGCCCGGCAGGCGGCGAGGCGGGTCGGGGAACG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35808042..35808151 26863196 MeRIP-seq:(Medium) rs1206319867 Functional Loss SNV dbSNP153 33..33 33 - - - 88297 RMVar_ID_88297 Human_SNP_ID_9369826 m1A Human chr1 - 35808124 35808124 35808124 CGGGAGCCAGCGCGCGCGCCCGCCGGGAGGGAAGGGGGCGCGGGGTGCGCGGACCCAGGGTCCCG CGGGAGCCAGCGCGCGCGCCCGCCGGGAGGGAGGGGGGCGCGGGGTGCGCGGACCCAGGGTCCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:35808092..35808179 26863196 MeRIP-seq:(Medium) rs1450942120 Functional Loss SNV dbSNP153 33..33 33 - - - 88298 RMVar_ID_88298 Human_SNP_ID_9369880 m1A Human chr1 + 35808225 35808225 35808225 GCGGGGATTGTTTTTGTTGTCGCTGAGGCCGGAAGAGCCGGAGCCGGGTCCCTGTCCCCGGGCCG GCGGGGATTGTTTTTGTTGTCGCTGAGGCCGGCAGAGCCGGAGCCGGGTCCCTGTCCCCGGGCCG A C AGO4 Ensembl:ENSG00000134698 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35808072..35808651 26863196 MeRIP-seq:(Medium) rs994188259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9319909 RMVar_hsa_circ_104871 88299 RMVar_ID_88299 Human_SNP_ID_9376575 m1A Human chr1 - 35835508 35835508 35835508 CTTCCCACATGACTGATTTAGCAAAAGAATCAATCTTCCCAGCTCCTCCCTCTCAGTACACACAC CTTCCCACATGACTGATTTAGCAAAAGAATCAGTCTTCCCAGCTCCTCCCTCTCAGTACACACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:35835471..35835600 26863196 MeRIP-seq:(Medium) rs777837450 Functional Loss SNV dbSNP153 33..33 33 - - - 88300 RMVar_ID_88300 Human_SNP_ID_9397559 m1A Human chr1 - 35924575 35924575 35924575 GCCTTATTCCACTCCCTCATTATCTTCCTCCTATGCCAGGGGACTATTTGGCTAATCATATCCCC GCCTTATTCCACTCCCTCATTATCTTCCTCCTGTGCCAGGGGACTATTTGGCTAATCATATCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35924524..35924883 26863196 MeRIP-seq:(Medium) rs1302643848 Functional Loss SNV dbSNP153 33..33 33 - - - 88301 RMVar_ID_88301 Human_SNP_ID_9399274 m1A Human chr1 - 35931373 35931370 35931373 TTCGAGGGAGAACGGAGCCCGCCACTGGCGGCAAGGAGGCGGCCCGGGGGGCGACGCGGCGCGAC TTCGAGGGAGAACGGAGCCCGCCACTGGCGGC___GAGGCGGCCCGGGGGGCGACGCGGCGCGAC CCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:35931291..35931395 26863196 MeRIP-seq:(Medium) rs1211593939 Functional Loss DEL dbSNP153 33..35 33 - - - 88302 RMVar_ID_88302 Human_SNP_ID_9399284 m1A Human chr1 - 35931390 35931390 35931390 GGAGCTGGGGGGAGTGCTTCGAGGGAGAACGGAGCCCGCCACTGGCGGCAAGGAGGCGGCCCGGG GGAGCTGGGGGGAGTGCTTCGAGGGAGAACGGGGCCCGCCACTGGCGGCAAGGAGGCGGCCCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:35931110..35931402 26863196 MeRIP-seq:(Medium) rs1165409376 Functional Loss SNV dbSNP153 33..33 33 - - - 88303 RMVar_ID_88303 Human_SNP_ID_9437183 m1A Human chr1 - 36088984 36088984 36088984 AGCCCACGCAGTCCCCGAGCAGCGCGCCAGCCAGGCAGCCTCGGAAGCGCGAGAGGGAGCGGGCC AGCCCACGCAGTCCCCGAGCAGCGCGCCAGCCTGGCAGCCTCGGAAGCGCGAGAGGGAGCGGGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36088935..36089045 26863196 MeRIP-seq:(Medium) rs1354995738 Functional Loss SNV dbSNP153 33..33 33 - - - 88304 RMVar_ID_88304 Human_SNP_ID_9438715 m1A Human chr1 - 36093675 36093675 36093675 ATCCCATGTCCAAGACAATACAGGAAAATGCCACAAGTACCCCTCCAAAATAAACCCGCCTGCGT ATCCCATGTCCAAGACAATACAGGAAAATGCCGCAAGTACCCCTCCAAAATAAACCCGCCTGCGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36093626..36093850 32194978 MeRIP-seq:(Medium) rs1372611878 Functional Loss SNV dbSNP153 33..33 33 - - - 88305 RMVar_ID_88305 Human_SNP_ID_9450737 m1A Human chr1 - 36140151 36140151 36140151 TTTTGAATCTCTTTTAGAGCTCTGAGCTCTTCACCCTGACCTATGGTGCCCTGGTCACCCAGCTA TTTTGAATCTCTTTTAGAGCTCTGAGCTCTTCCCCCTGACCTATGGTGCCCTGGTCACCCAGCTA T G TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:36140101..36140175 26863196 MeRIP-seq:(Medium) rs913419027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849831,Human_RBP_ID_4048853,Human_RBP_ID_8939965,Human_RBP_ID_9518346,Human_RBP_ID_10965426,Human_RBP_ID_22636733,Human_RBP_ID_22734668 Human_Splice_Rec_47446,Human_Splice_Rec_47447,Human_Splice_Rec_47454,Human_Splice_Rec_47455,Human_Splice_Rec_47462,Human_Splice_Rec_47463,Human_Splice_Rec_47469,Human_Splice_Rec_47474,Human_Splice_Rec_47475,Human_Splice_Rec_47482,Human_Splice_Rec_47483,Human_Splice_Rec_47492,Human_Splice_Rec_47493,Human_Splice_Rec_47500,Human_Splice_Rec_47501 RMVar_hsa_circ_29890,RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_349038,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667 88306 RMVar_ID_88306 Human_SNP_ID_9453139 m1A Human chr1 - 36149381 36149381 36149381 CGTGGCTAGGCGAGTGGGGCGGGGCGGCCGGCACCATGTCGAGGCAGGCGAACCGTGGCACCGAG CGTGGCTAGGCGAGTGGGGCGGGGCGGCCGGCGCCATGTCGAGGCAGGCGAACCGTGGCACCGAG T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:36149351..36149475 26863410 MeRIP-seq:(Medium) rs758525156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741432,Human_RBP_ID_800978,Human_RBP_ID_4072702,Human_RBP_ID_9319913,Human_RBP_ID_17750119,Human_RBP_ID_18965228,Human_RBP_ID_22636734,Human_RBP_ID_23205873 Human_Splice_Rec_47441,Human_Splice_Rec_47445,Human_Splice_Rec_47461,Human_Splice_Rec_47489,Human_Splice_Rec_47491 RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_77753,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667,RMVar_hsa_circ_131668 88307 RMVar_ID_88307 Human_SNP_ID_9453166 m1A Human chr1 + 36149435 36149435 36149435 GCCTAGCCACGGGTTAGCTCGGCGACCCCTGCAGACGCCGGAGCCTAAGCCGCTGCCCCTCAGCC GCCTAGCCACGGGTTAGCTCGGCGACCCCTGCCGACGCCGGAGCCTAAGCCGCTGCCCCTCAGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36149193..36149500 26863196 MeRIP-seq:(Medium) rs1422352692 Functional Loss SNV dbSNP153 33..33 33 - - - 88308 RMVar_ID_88308 Human_SNP_ID_9453167 m1A Human chr1 + 36149435 36149435 36149435 GCCTAGCCACGGGTTAGCTCGGCGACCCCTGCAGACGCCGGAGCCTAAGCCGCTGCCCCTCAGCC GCCTAGCCACGGGTTAGCTCGGCGACCCCTGCGGACGCCGGAGCCTAAGCCGCTGCCCCTCAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36149193..36149500 26863196 MeRIP-seq:(Medium) rs1422352692 Functional Loss SNV dbSNP153 33..33 33 - - - 88309 RMVar_ID_88309 Human_SNP_ID_9453171 m1A Human chr1 + 36149444 36149444 36149444 CGGGTTAGCTCGGCGACCCCTGCAGACGCCGGAGCCTAAGCCGCTGCCCCTCAGCCCACAAGACC CGGGTTAGCTCGGCGACCCCTGCAGACGCCGGGGCCTAAGCCGCTGCCCCTCAGCCCACAAGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:36149314..36149500 26863196 MeRIP-seq:(Medium) rs1033096289 Functional Loss SNV dbSNP153 33..33 33 - - - 88310 RMVar_ID_88310 Human_SNP_ID_9458453 m1A Human chr1 + 36170908 36170908 36170908 GAAGAAGTCGGTTGAACAAGGGAGAGGGCCACATATGGGGCTGATGGCACAGATGAGCAATCTGA GAAGAAGTCGGTTGAACAAGGGAGAGGGCCACTTATGGGGCTGATGGCACAGATGAGCAATCTGA A T MAP7D1 Ensembl:ENSG00000116871 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:36170904..36171136 26863410 MeRIP-seq:(Medium) rs954502716 Functional Loss SNV dbSNP153 33..33 33 - - - 88311 RMVar_ID_88311 Human_SNP_ID_9458501 m1A Human chr1 - 36171024 36171024 36171024 GACCAGGGCTGACATTGGTGGTGGTGGGGGGGAAGGGTCACCTTCTGGAGAAGGTCTTGGCTCTG GACCAGGGCTGACATTGGTGGTGGTGGGGGGGGAGGGTCACCTTCTGGAGAAGGTCTTGGCTCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr1:36170879..36171600;chr1:36170896..36171182;chr1:36170935..36171250;chr1:36170919..36171088 26863196 MeRIP-seq:(Medium) rs200289388 Functional Loss SNV dbSNP153 33..33 33 - - - 88312 RMVar_ID_88312 Human_SNP_ID_9458502 m1A Human chr1 - 36171024 36171024 36171024 GACCAGGGCTGACATTGGTGGTGGTGGGGGGGAAGGGTCACCTTCTGGAGAAGGTCTTGGCTCTG GACCAGGGCTGACATTGGTGGTGGTGGGGGGGCAGGGTCACCTTCTGGAGAAGGTCTTGGCTCTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr1:36170879..36171600;chr1:36170896..36171182;chr1:36170935..36171250;chr1:36170919..36171088 26863196 MeRIP-seq:(Medium) rs200289388 Functional Loss SNV dbSNP153 33..33 33 - - - 88313 RMVar_ID_88313 Human_SNP_ID_9458518 m1A Human chr1 + 36171042 36171042 36171042 CAGAAGGTGACCCTTCCCCCCCACCACCACCAATGTCAGCCCTGGTCCCCGACACTCCCCCGGAC CAGAAGGTGACCCTTCCCCCCCACCACCACCAGTGTCAGCCCTGGTCCCCGACACTCCCCCGGAC A G MAP7D1 Ensembl:ENSG00000116871 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36170899..36171157 26863196 MeRIP-seq:(Medium) rs200505073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26863860 Human_Splice_Rec_47504,Human_Splice_Rec_47514,Human_Splice_Rec_47544,Human_Splice_Rec_47548,Human_Splice_Rec_47582,Human_Splice_Rec_47614 RMVar_hsa_circ_43874,RMVar_hsa_circ_52096,RMVar_hsa_circ_312622,RMVar_hsa_circ_367803,RMVar_hsa_circ_105619,RMVar_hsa_circ_49986,RMVar_hsa_circ_131669,RMVar_hsa_circ_131670,RMVar_hsa_circ_131671 88314 RMVar_ID_88314 Human_SNP_ID_9458519 m1A Human chr1 + 36171042 36171042 36171042 CAGAAGGTGACCCTTCCCCCCCACCACCACCAATGTCAGCCCTGGTCCCCGACACTCCCCCGGAC CAGAAGGTGACCCTTCCCCCCCACCACCACCATTGTCAGCCCTGGTCCCCGACACTCCCCCGGAC A T MAP7D1 Ensembl:ENSG00000116871 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36170899..36171157 26863196 MeRIP-seq:(Medium) rs200505073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26863860 Human_Splice_Rec_47504,Human_Splice_Rec_47514,Human_Splice_Rec_47544,Human_Splice_Rec_47548,Human_Splice_Rec_47582,Human_Splice_Rec_47614 RMVar_hsa_circ_43874,RMVar_hsa_circ_52096,RMVar_hsa_circ_312622,RMVar_hsa_circ_367803,RMVar_hsa_circ_105619,RMVar_hsa_circ_49986,RMVar_hsa_circ_131669,RMVar_hsa_circ_131670,RMVar_hsa_circ_131671 88315 RMVar_ID_88315 Human_SNP_ID_9459004 m1A Human chr1 - 36172512 36172512 36172512 GGCGCCGGCGCTCCTGGAGCTGCTTCTCCCGCAGCGCCTTGGCCTTCTCCTCCTTCTCCAGCCAC GGCGCCGGCGCTCCTGGAGCTGCTTCTCCCGCGGCGCCTTGGCCTTCTCCTCCTTCTCCAGCCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:36172423..36173467 26863196 MeRIP-seq:(Medium) rs746338261 Functional Loss SNV dbSNP153 33..33 33 - - - 88316 RMVar_ID_88316 Human_SNP_ID_9459228 m1A Human chr1 - 36173344 36173344 36173344 CTTCATAGCGCTCCTGGGGGAAGGTGGGGAGAAGAGAGAGATGTGGACTCAGAACATTCATCGAA CTTCATAGCGCTCCTGGGGGAAGGTGGGGAGACGAGAGAGATGTGGACTCAGAACATTCATCGAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36172412..36176263 26863196 MeRIP-seq:(Medium) rs1443984636 Functional Loss SNV dbSNP153 33..33 33 - - - 88317 RMVar_ID_88317 Human_SNP_ID_9459254 m1A Human chr1 + 36173401 36173401 36173401 CTATGAAGCAGCCATCCAACGGTCAGTGAAGAAGACGTGGGCCGAAATCCGGCAGCAGCGCTGGT CTATGAAGCAGCCATCCAACGGTCAGTGAAGAGGACGTGGGCCGAAATCCGGCAGCAGCGCTGGT A G MAP7D1 Ensembl:ENSG00000116871 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36172470..36177501 32194978 MeRIP-seq:(Medium) rs1242416418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354037,Human_RBP_ID_5159328,Human_RBP_ID_26310852 Human_Splice_Rec_47510,Human_Splice_Rec_47511,Human_Splice_Rec_47520,Human_Splice_Rec_47521,Human_Splice_Rec_47554,Human_Splice_Rec_47555,Human_Splice_Rec_47588,Human_Splice_Rec_47589,Human_Splice_Rec_47620,Human_Splice_Rec_47622,Human_Splice_Rec_47623 Human_miRNA_ID_2377164,Human_miRNA_ID_3092241 RMVar_hsa_circ_43874,RMVar_hsa_circ_52096,RMVar_hsa_circ_312622,RMVar_hsa_circ_105619,RMVar_hsa_circ_131670,RMVar_hsa_circ_131671 88318 RMVar_ID_88318 Human_SNP_ID_9460258 m1A Human chr1 + 36176722 36176722 36176722 CTGCCAGGTGCAGAAAAAGGAGAAGAAGGACAAGGAGCGGGAAAACGAGAAGGAGAAGAGTGCCC CTGCCAGGTGCAGAAAAAGGAGAAGAAGGACAGGGAGCGGGAAAACGAGAAGGAGAAGAGTGCCC A G MAP7D1 Ensembl:ENSG00000116871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36176701..36176725 26863196 MeRIP-seq:(Medium) rs751911313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_47524,Human_Splice_Rec_47562,Human_Splice_Rec_47594,Human_Splice_Rec_47628 RMVar_hsa_circ_43874,RMVar_hsa_circ_52096,RMVar_hsa_circ_105619,RMVar_hsa_circ_131671 88319 RMVar_ID_88319 Human_SNP_ID_9460259 m1A Human chr1 + 36176722 36176722 36176722 CTGCCAGGTGCAGAAAAAGGAGAAGAAGGACAAGGAGCGGGAAAACGAGAAGGAGAAGAGTGCCC CTGCCAGGTGCAGAAAAAGGAGAAGAAGGACATGGAGCGGGAAAACGAGAAGGAGAAGAGTGCCC A T MAP7D1 Ensembl:ENSG00000116871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36176701..36176725 26863196 MeRIP-seq:(Medium) rs751911313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_47524,Human_Splice_Rec_47562,Human_Splice_Rec_47594,Human_Splice_Rec_47628 RMVar_hsa_circ_43874,RMVar_hsa_circ_52096,RMVar_hsa_circ_105619,RMVar_hsa_circ_131671 88320 RMVar_ID_88320 Human_SNP_ID_9460639 m1A Human chr1 - 36177833 36177829 36177833 AAAAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCT AAAAGGGAAAAGGGAAGGGTTAGGAGACACAC____CCACACGCTGAGAACTTGTTCCTTCCTCT GGTGT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:36177831..36177950 26863410 MeRIP-seq:(Medium) rs772459167 Functional Loss DEL dbSNP153 33..36 33 - - - 88321 RMVar_ID_88321 Human_SNP_ID_9460640 m1A Human chr1 - 36177833 36177829 36177833 AAAAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCT AAAAGGGAAAAGGGAAGGGTTAGGAGACACAC__ACCCACACGCTGAGAACTTGTTCCTTCCTCT GGTGT GGT - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:36177831..36177950 26863410 MeRIP-seq:(Medium) rs772459167 Functional Loss DEL dbSNP153 33..34 33 - - - 88322 RMVar_ID_88322 Human_SNP_ID_9460643 m1A Human chr1 - 36177831 36177831 36177831 AAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCTGG AAGGGAAAAGGGAAGGGTTAGGAGACACACACGCCCACACGCTGAGAACTTGTTCCTTCCTCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36177829..36178225 26863196 MeRIP-seq:(Medium) rs1462224441 Functional Loss SNV dbSNP153 33..33 33 - - - 88323 RMVar_ID_88323 Human_SNP_ID_9460644 m1A Human chr1 - 36177831 36177831 36177831 AAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCTGG AAGGGAAAAGGGAAGGGTTAGGAGACACACACCCCCACACGCTGAGAACTTGTTCCTTCCTCTGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36177829..36178225 26863196 MeRIP-seq:(Medium) rs1462224441 Functional Loss SNV dbSNP153 33..33 33 - - - 88324 RMVar_ID_88324 Human_SNP_ID_9460645 m1A Human chr1 - 36177833 36177833 36177833 AAAAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCT AAAAGGGAAAAGGGAAGGGTTAGGAGACACACGCACCCACACGCTGAGAACTTGTTCCTTCCTCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:36177831..36177950 26863410 MeRIP-seq:(Medium) rs765047202 Functional Loss SNV dbSNP153 33..33 33 - - - 88325 RMVar_ID_88325 Human_SNP_ID_9460646 m1A Human chr1 - 36177833 36177833 36177833 AAAAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCT AAAAGGGAAAAGGGAAGGGTTAGGAGACACACCCACCCACACGCTGAGAACTTGTTCCTTCCTCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:36177831..36177950 26863410 MeRIP-seq:(Medium) rs765047202 Functional Loss SNV dbSNP153 33..33 33 - - - 88326 RMVar_ID_88326 Human_SNP_ID_9460684 m1A Human chr1 + 36177951 36177951 36177951 AGGCCTGCCTCCCCCTGCCCCAGCCCAGGGCCAGGCCACACTCTGCCTCCAAAGCCACCGTCCCC AGGCCTGCCTCCCCCTGCCCCAGCCCAGGGCCCGGCCACACTCTGCCTCCAAAGCCACCGTCCCC A C MAP7D1 Ensembl:ENSG00000116871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36177926..36177950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_354040,Human_RBP_ID_9270055,Human_RBP_ID_22532108,Human_RBP_ID_22558643,Human_RBP_ID_22636739 Human_Splice_Rec_47526,Human_Splice_Rec_47564,Human_Splice_Rec_47596,Human_Splice_Rec_47630,Human_Splice_Rec_47636,Human_Splice_Rec_47644 Human_miRNA_ID_1300823,Human_miRNA_ID_1769986,Human_miRNA_ID_2426130,Human_miRNA_ID_2473920,Human_miRNA_ID_2909585,Human_miRNA_ID_2959706 RMVar_hsa_circ_43874,RMVar_hsa_circ_105619,RMVar_hsa_circ_131671 88327 RMVar_ID_88327 Human_SNP_ID_9460692 m1A Human chr1 - 36177962 36177962 36177962 TGGTGCCTCGGGGGGACGGTGGCTTTGGAGGCAGAGTGTGGCCTGGCCCTGGGCTGGGGCAGGGG TGGTGCCTCGGGGGGACGGTGGCTTTGGAGGCTGAGTGTGGCCTGGCCCTGGGCTGGGGCAGGGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36177876..36178025 32194978 MeRIP-seq:(Medium) rs1370213032 Functional Loss SNV dbSNP153 33..33 33 - - - 88328 RMVar_ID_88328 Human_SNP_ID_9460693 m1A Human chr1 - 36177962 36177962 36177962 TGGTGCCTCGGGGGGACGGTGGCTTTGGAGGCAGAGTGTGGCCTGGCCCTGGGCTGGGGCAGGGG TGGTGCCTCGGGGGGACGGTGGCTTTGGAGGCGGAGTGTGGCCTGGCCCTGGGCTGGGGCAGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36177876..36178025 32194978 MeRIP-seq:(Medium) rs1370213032 Functional Loss SNV dbSNP153 33..33 33 - - - 88329 RMVar_ID_88329 Human_SNP_ID_9460773 m1A Human chr1 - 36178123 36178123 36178123 GGTGGGCGAGGGCGCCGGCGAAGGTGCCGGTGAGGCTGGGGCTGCTGACTCCTTCTCGTTACTGG GGTGGGCGAGGGCGCCGGCGAAGGTGCCGGTGGGGCTGGGGCTGCTGACTCCTTCTCGTTACTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:36178076..36178175 26863196 MeRIP-seq:(Medium) rs1463559751 Functional Loss SNV dbSNP153 33..33 33 - - - 88330 RMVar_ID_88330 Human_SNP_ID_9461057 m1A Human chr1 + 36178772 36178772 36178772 GCGGAGGCCCGGAGGCGGGAGGAGCAGGAGGCACGAGAGAAGGCGCAGGCCGAGCAGGAGGAGCA GCGGAGGCCCGGAGGCGGGAGGAGCAGGAGGCGCGAGAGAAGGCGCAGGCCGAGCAGGAGGAGCA A G MAP7D1 Ensembl:ENSG00000116871 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:36178676..36178775 26863196 MeRIP-seq:(Medium) rs1163342052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804337 Human_Splice_Rec_47530,Human_Splice_Rec_47531,Human_Splice_Rec_47568,Human_Splice_Rec_47569,Human_Splice_Rec_47600,Human_Splice_Rec_47601,Human_Splice_Rec_47634,Human_Splice_Rec_47640,Human_Splice_Rec_47641,Human_Splice_Rec_47648,Human_Splice_Rec_47649 Human_miRNA_ID_3115483 RMVar_hsa_circ_43874,RMVar_hsa_circ_105619,RMVar_hsa_circ_131671 88331 RMVar_ID_88331 Human_SNP_ID_9461306 m1A Human chr1 - 36179288 36179288 36179288 CTGACCTTGGTTTCAGAAACTTCTGACTTCCGAGTCCTCTTCATGATCTCCTCCAGACGCTGTTT CTGACCTTGGTTTCAGAAACTTCTGACTTCCGTGTCCTCTTCATGATCTCCTCCAGACGCTGTTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36179251..36179325 26863196 MeRIP-seq:(Medium) rs199901837 Functional Loss SNV dbSNP153 33..33 33 - - - 88332 RMVar_ID_88332 Human_SNP_ID_9461307 m1A Human chr1 - 36179288 36179288 36179288 CTGACCTTGGTTTCAGAAACTTCTGACTTCCGAGTCCTCTTCATGATCTCCTCCAGACGCTGTTT CTGACCTTGGTTTCAGAAACTTCTGACTTCCGGGTCCTCTTCATGATCTCCTCCAGACGCTGTTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36179251..36179325 26863196 MeRIP-seq:(Medium) rs199901837 Functional Loss SNV dbSNP153 33..33 33 - - - 88333 RMVar_ID_88333 Human_SNP_ID_9473826 m1A Human chr1 + 36224487 36224487 36224487 GGCTGGTTGTTCCGTTGCGAGCTGCAGCTGCGATCTCTGTGGTAGGCCCAGGTGAGTGAGCGCCT GGCTGGTTGTTCCGTTGCGAGCTGCAGCTGCGGTCTCTGTGGTAGGCCCAGGTGAGTGAGCGCCT A G THRAP3 Ensembl:ENSG00000054118 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:36224426..36224546;chr1:36224401..36224627 26863196 MeRIP-seq:(Medium) rs1396334171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741433,Human_RBP_ID_1430603,Human_RBP_ID_4073872,Human_RBP_ID_5311643,Human_RBP_ID_8309980,Human_RBP_ID_8754921,Human_RBP_ID_8969638,Human_RBP_ID_9318837,Human_RBP_ID_10965835,Human_RBP_ID_18414927,Human_RBP_ID_18573689,Human_RBP_ID_19034549,Human_RBP_ID_22430443 Human_Splice_Rec_47673,Human_Splice_Rec_47695,Human_Splice_Rec_47719 Human_miRNA_ID_2054423 RMVar_hsa_circ_81186,RMVar_hsa_circ_131672 88334 RMVar_ID_88334 Human_SNP_ID_9474581 m1A Human chr1 + 36227019 36227019 36227019 CCTAAGGGTGGTCAGTGAAGTTCTTTTTGGGGAGAGTGAGGAAACCAATTTGTAGGATGTCAAGG CCTAAGGGTGGTCAGTGAAGTTCTTTTTGGGGCGAGTGAGGAAACCAATTTGTAGGATGTCAAGG A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:36227001..36227130 26863196 MeRIP-seq:(Medium) rs901084961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2145695,Human_RBP_ID_5818693,Human_RBP_ID_9518395,Human_RBP_ID_10965974 RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 88335 RMVar_ID_88335 Human_SNP_ID_9474582 m1A Human chr1 + 36227019 36227019 36227019 CCTAAGGGTGGTCAGTGAAGTTCTTTTTGGGGAGAGTGAGGAAACCAATTTGTAGGATGTCAAGG CCTAAGGGTGGTCAGTGAAGTTCTTTTTGGGGGGAGTGAGGAAACCAATTTGTAGGATGTCAAGG A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:36227001..36227130 26863196 MeRIP-seq:(Medium) rs901084961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2145695,Human_RBP_ID_5818693,Human_RBP_ID_9518395,Human_RBP_ID_10965974 RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 88336 RMVar_ID_88336 Human_SNP_ID_9492417 m1A Human chr1 - 36289351 36289351 36289351 TTAGACATAAATTTGGGTTCATCATCAAACTCAGATTCCTTTCTTCCCTTAGCTTTGTCCTTATC TTAGACATAAATTTGGGTTCATCATCAAACTCGGATTCCTTTCTTCCCTTAGCTTTGTCCTTATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:36289301..36289575;chr1:36289301..36289550 26863196 MeRIP-seq:(Medium) rs1332994581 Functional Loss SNV dbSNP153 33..33 33 - - - 88337 RMVar_ID_88337 Human_SNP_ID_9492420 m1A Human chr1 - 36289356 36289356 36289356 TGACTTTAGACATAAATTTGGGTTCATCATCAAACTCAGATTCCTTTCTTCCCTTAGCTTTGTCC TGACTTTAGACATAAATTTGGGTTCATCATCAGACTCAGATTCCTTTCTTCCCTTAGCTTTGTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36289306..36289406 32194978 MeRIP-seq:(Medium) rs1286770415 Functional Loss SNV dbSNP153 33..33 33 - - - 88338 RMVar_ID_88338 Human_SNP_ID_9495734 m1A Human chr1 - 36300878 36300876 36300878 CCTGTCTCTTGCTCTCCGATGCTTCCTGTGAAAAGAGAAGAGCCAGGGTGATCAATCATCTTTCT CCTGTCTCTTGCTCTCCGATGCTTCCTGTGAA__GAGAAGAGCCAGGGTGATCAATCATCTTTCT CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:36300876..36300925 26863196 MeRIP-seq:(Medium) rs765236765 Functional Loss DEL dbSNP153 33..34 33 - - - 88339 RMVar_ID_88339 Human_SNP_ID_9495735 m1A Human chr1 - 36300878 36300876 36300878 CCTGTCTCTTGCTCTCCGATGCTTCCTGTGAAAAGAGAAGAGCCAGGGTGATCAATCATCTTTCT CCTGTCTCTTGCTCTCCGATGCTTCCTGTGAA_AGAGAAGAGCCAGGGTGATCAATCATCTTTCT CTT CT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:36300876..36300925 26863196 MeRIP-seq:(Medium) rs765236765 Functional Loss DEL dbSNP153 33..33 33 - - - 88340 RMVar_ID_88340 Human_SNP_ID_9495945 m1A Human chr1 + 36301619 36301617 36301620 GCAACTACTCTGGGAACAATAACAACAACAGCAACAACGATTTTCAAAAAAGAAACCGGGAAGAG GCAACTACTCTGGGAACAATAACAACAACAG___CAACGATTTTCAAAAAAGAAACCGGGAAGAG GCAA G THRAP3 Ensembl:ENSG00000054118 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36300978..36301700 26863196 MeRIP-seq:(Medium) rs1367571979 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17010,Human_RBP_ID_1430749,Human_RBP_ID_1747077,Human_RBP_ID_8227979,Human_RBP_ID_8240803,Human_RBP_ID_17218330,Human_RBP_ID_17646346,Human_RBP_ID_18523221,Human_RBP_ID_18573822,Human_RBP_ID_27800079 Human_Splice_Rec_47692,Human_Splice_Rec_47693,Human_Splice_Rec_47714,Human_Splice_Rec_47715,Human_Splice_Rec_47736,Human_Splice_Rec_47737 RMVar_hsa_circ_127926,RMVar_hsa_circ_131676,RMVar_hsa_circ_71646,RMVar_hsa_circ_54612,RMVar_hsa_circ_69610,RMVar_hsa_circ_84472,RMVar_hsa_circ_131684,RMVar_hsa_circ_365466 88341 RMVar_ID_88341 Human_SNP_ID_9496553 m1A Human chr1 + 36303898 36303898 36303898 GGGGTCGGGGCCGGTTCATGTTCCGGAAATCAAGTACCAGCCCCAAGTGGGCCCATGACAAGTTC GGGGTCGGGGCCGGTTCATGTTCCGGAAATCAGGTACCAGCCCCAAGTGGGCCCATGACAAGTTC A G THRAP3 Ensembl:ENSG00000054118 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:36303876..36303900 26863196 MeRIP-seq:(Medium) rs1457513013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354080,Human_RBP_ID_1430751,Human_RBP_ID_2145859,Human_RBP_ID_8969676,Human_RBP_ID_10968173,Human_RBP_ID_22784852,Human_RBP_ID_23392112 Human_miRNA_ID_2478054 RMVar_hsa_circ_127926,RMVar_hsa_circ_131676,RMVar_hsa_circ_84472,RMVar_hsa_circ_131684,RMVar_hsa_circ_82517,RMVar_hsa_circ_131687 88342 RMVar_ID_88342 Human_SNP_ID_9496566 m1A Human chr1 + 36303938 36303938 36303938 CCCCAAGTGGGCCCATGACAAGTTCAGTGGGGAGGAAGGGGAGATTGAAGACGACGAGAGTGGGA CCCCAAGTGGGCCCATGACAAGTTCAGTGGGGCGGAAGGGGAGATTGAAGACGACGAGAGTGGGA A C THRAP3 Ensembl:ENSG00000054118 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36300995..36304211 32194978 MeRIP-seq:(Medium) rs369494643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17012,Human_RBP_ID_849842,Human_RBP_ID_978019,Human_RBP_ID_1747080,Human_RBP_ID_4049150,Human_RBP_ID_5109077,Human_RBP_ID_5819187,Human_RBP_ID_9356044,Human_RBP_ID_10968174,Human_RBP_ID_23112420,Human_RBP_ID_24541085,Human_RBP_ID_24692921,Human_RBP_ID_26310873,Human_RBP_ID_26863969,Human_RBP_ID_27800081 RMVar_hsa_circ_127926,RMVar_hsa_circ_131676,RMVar_hsa_circ_84472,RMVar_hsa_circ_131684,RMVar_hsa_circ_82517,RMVar_hsa_circ_131687 88343 RMVar_ID_88343 Human_SNP_ID_9496569 m1A Human chr1 + 36303956 36303954 36303957 CAAGTTCAGTGGGGAGGAAGGGGAGATTGAAGACGACGAGAGTGGGACAGAGAACCGAGAAGAGA CAAGTTCAGTGGGGAGGAAGGGGAGATTGAA___GACGAGAGTGGGACAGAGAACCGAGAAGAGA AGAC A THRAP3 Ensembl:ENSG00000054118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:36303776..36304216;chr1:36301518..36304182 26863196 MeRIP-seq:(Medium) rs766680277 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17012,Human_RBP_ID_800989,Human_RBP_ID_849842,Human_RBP_ID_1064287,Human_RBP_ID_1747080,Human_RBP_ID_2145860,Human_RBP_ID_4049150,Human_RBP_ID_5109077,Human_RBP_ID_5162261,Human_RBP_ID_5537771,Human_RBP_ID_5819187,Human_RBP_ID_8748726,Human_RBP_ID_9356044,Human_RBP_ID_10968174,Human_RBP_ID_18543951,Human_RBP_ID_22875100,Human_RBP_ID_23112420,Human_RBP_ID_24541085,Human_RBP_ID_26310873,Human_RBP_ID_26863969,Human_RBP_ID_27800081 RMVar_hsa_circ_127926,RMVar_hsa_circ_131676,RMVar_hsa_circ_84472,RMVar_hsa_circ_131684,RMVar_hsa_circ_82517,RMVar_hsa_circ_131687 88344 RMVar_ID_88344 Human_SNP_ID_9497355 m1A Human chr1 - 36306618 36306618 36306618 CAGACTCAGCTCGTCCTCCTTCTGCGCGCGGTATCCGGCCAGGACGAGGACTTCTGCGGGCGGAA CAGACTCAGCTCGTCCTCCTTCTGCGCGCGGTCTCCGGCCAGGACGAGGACTTCTGCGGGCGGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:36306609..36306783;chr1:36306609..36306709 26863196 MeRIP-seq:(Medium) rs1395737514 Functional Loss SNV dbSNP153 33..33 33 - - - 88345 RMVar_ID_88345 Human_SNP_ID_9501112 m1A Human chr1 + 36319772 36319754 36319773 TGCCACCCCAGAGAGGCCCCCAGCTCCAGAGAACGCCCCCAGCTCCAAGAAGATCCCGGCTCCTG TGCCACCCCAGAGAG___________________GCCCCCAGCTCCAAGAAGATCCCGGCTCCTG GGCCCCCAGCTCCAGAGAAC G SH3D21 Ensembl:ENSG00000214193 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36319534..36319859 26863196 MeRIP-seq:(Medium) rs751719042 Functional Loss DEL dbSNP153 16..34 33 - - - Human_Splice_Rec_47770,Human_Splice_Rec_47792,Human_Splice_Rec_47808 88346 RMVar_ID_88346 Human_SNP_ID_9501272 m1A Human chr1 + 36320169 36320169 36320169 GAAGAAGAGGTGTCCACCAGAGATGACATTCAATTCCATCACTTCTCTTCGGAGGAAGCCCTGCA GAAGAAGAGGTGTCCACCAGAGATGACATTCAGTTCCATCACTTCTCTTCGGAGGAAGCCCTGCA A G SH3D21 Ensembl:ENSG00000214193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36320119..36320220 32194978 MeRIP-seq:(Medium) rs1380494058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17677732,Human_RBP_ID_18573850 88347 RMVar_ID_88347 Human_SNP_ID_9501594 m1A Human chr1 + 36320798 36320798 36320798 GAGGGCGCTGGAGCTGATGGAGGTGCAGCTGGAGTGAGTGGGCAGTGGCGGGGGTTGTGGAAGGT GAGGGCGCTGGAGCTGATGGAGGTGCAGCTGGTGTGAGTGGGCAGTGGCGGGGGTTGTGGAAGGT A T SH3D21 Ensembl:ENSG00000214193 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36320213..36321206 26863196 MeRIP-seq:(Medium) rs560972819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18968001 Human_Splice_Rec_47771,Human_Splice_Rec_47793,Human_Splice_Rec_47809,Human_Splice_Rec_47827,Human_Splice_Rec_47835 88348 RMVar_ID_88348 Human_SNP_ID_9501673 m1A Human chr1 + 36320955 36320955 36320955 TGACCGACATCTGGGAGGAGCTGAAGAGCGAGAAGGAGCAGCGCCGGCGGCTGGAGGTGAGGCGC TGACCGACATCTGGGAGGAGCTGAAGAGCGAGGAGGAGCAGCGCCGGCGGCTGGAGGTGAGGCGC A G SH3D21 Ensembl:ENSG00000214193 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:36320303..36321224 26863196 MeRIP-seq:(Medium) rs1384239841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854414,Human_RBP_ID_18965235,Human_RBP_ID_22871762,Human_RBP_ID_26310882,Human_RBP_ID_27797826 Human_Splice_Rec_47772,Human_Splice_Rec_47773,Human_Splice_Rec_47794,Human_Splice_Rec_47795,Human_Splice_Rec_47810,Human_Splice_Rec_47811,Human_Splice_Rec_47828,Human_Splice_Rec_47829,Human_Splice_Rec_47836,Human_Splice_Rec_47837 88349 RMVar_ID_88349 Human_SNP_ID_9502772 m1A Human chr1 - 36323893 36323890 36323894 TAATGGTATCACGTCGCAGGGTTGTCAGGCGGAGTAAGTGAAAGAACCTGTCCAAGGTTTAGCCC TAATGGTATCACGTCGCAGGGTTGTCAGGCG____AAGTGAAAGAACCTGTCCAAGGTTTAGCCC TACTC T EVA1B Ensembl:ENSG00000142694 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36323846..36323951 32194978 MeRIP-seq:(Medium) rs1482109482 Functional Loss DEL dbSNP153 32..35 33 - - - Human_Splice_Rec_47847 88350 RMVar_ID_88350 Human_SNP_ID_9502890 m1A Human chr1 - 36324290 36324282 36324290 TCTGCCACAAGCCGCCACAAGCTGCTTGGTGCACAAGAGCGCAGGAGCTCGCAGGCACAGAGGCC TCTGCCACAAGCCGCCACAAGCTGCTTGGTGC________GCAGGAGCTCGCAGGCACAGAGGCC CGCTCTTGT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:36324239..36324687 32194978 MeRIP-seq:(Medium) rs927703125 Functional Loss DEL dbSNP153 33..40 33 - - - 88351 RMVar_ID_88351 Human_SNP_ID_9503503 m1A Human chr1 + 36326635 36326635 36326635 GACACATTTTGGAAAGATCCCTGTGGTGGCTCAGTGTAGGGTGGGCCACTGTGGGCAAGAAGGGG GACACATTTTGGAAAGATCCCTGTGGTGGCTCCGTGTAGGGTGGGCCACTGTGGGCAAGAAGGGG A C SH3D21 Ensembl:ENSG00000214193 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36326595..36326846 26863196 MeRIP-seq:(Medium) rs1037164035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5160556 88352 RMVar_ID_88352 Human_SNP_ID_9519112 m1A Human chr1 + 36385855 36385855 36385855 CGAGCCTCTCACCGCCGCCTCCCAGCGCAGCCACCCGAGCCGCCGCCGCCGCCGCCGCCGCCTCC CGAGCCTCTCACCGCCGCCTCCCAGCGCAGCCCCCCGAGCCGCCGCCGCCGCCGCCGCCGCCTCC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:36385796..36385883 26863410 MeRIP-seq:(Medium) rs1003335568 Functional Loss SNV dbSNP153 33..33 33 - - - 88353 RMVar_ID_88353 Human_SNP_ID_9522251 m1A Human chr1 + 36397860 36397860 36397860 CTGGCTGCCTCCCGCCGGCTGCAGCAGGACGGAGAAACCATGCCGGCGACCGGGCCGCTCTGTCC CTGGCTGCCTCCCGCCGGCTGCAGCAGGACGGGGAAACCATGCCGGCGACCGGGCCGCTCTGTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36397706..36397900 26863196 MeRIP-seq:(Medium) rs1300455173 Functional Loss SNV dbSNP153 33..33 33 - - - 88354 RMVar_ID_88354 Human_SNP_ID_9536899 m1A Human chr1 - 36455866 36455863 36455866 AAGCGAAGAAGAGCCTTAAAGGCTGCAGCAGCAGCCCAAAAACAAGCAAAGCGGAGGAACCCAGA AAGCGAAGAAGAGCCTTAAAGGCTGCAGCAGC___CCAAAAACAAGCAAAGCGGAGGAACCCAGA GGCT G MRPS15 Ensembl:ENSG00000116898 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36455816..36456424 32194978 MeRIP-seq:(Medium) rs750095902 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_354195,Human_RBP_ID_9356052,Human_RBP_ID_26310886,Human_RBP_ID_27800090 Human_Splice_Rec_48102,Human_Splice_Rec_48106,Human_Splice_Rec_48108,Human_Splice_Rec_48114 RMVar_hsa_circ_83664,RMVar_hsa_circ_131708 88355 RMVar_ID_88355 Human_SNP_ID_9537471 m1A Human chr1 + 36457978 36457978 36457978 CTTCATAACTGCGGATCTTGACAGACAAGGCAATAACTGAAACCACAAACCACAGAGGATGAGAG CTTCATAACTGCGGATCTTGACAGACAAGGCAGTAACTGAAACCACAAACCACAGAGGATGAGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36457927..36458027 32194978 MeRIP-seq:(Medium) rs749482343 Functional Loss SNV dbSNP153 33..33 33 - - - 88356 RMVar_ID_88356 Human_SNP_ID_9538417 m1A Human chr1 + 36461955 36461953 36461956 TTGCTGACCACCCACCCTCACCACACCTGGACACCTGGGCCCCTGCCTCCTTCTAGATCAAGCTT TTGCTGACCACCCACCCTCACCACACCTGGA___CTGGGCCCCTGCCTCCTTCTAGATCAAGCTT ACAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:36461953..36462051 26863196 MeRIP-seq:(Medium) rs1365828688 Functional Loss DEL dbSNP153 32..34 33 - - - 88357 RMVar_ID_88357 Human_SNP_ID_9538910 m1A Human chr1 + 36463841 36463838 36463841 GTTTCCGGACGACATATCCGCGCGCGGCCTGGAGGAGGAGACCTACGCAGAAAAGAGAGGGCTGA GTTTCCGGACGACATATCCGCGCGCGGCCT___GGAGGAGACCTACGCAGAAAAGAGAGGGCTGA TGGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:36462104..36464375 32194978 MeRIP-seq:(Medium) rs759392307 Functional Loss DEL dbSNP153 31..33 33 - - - 88358 RMVar_ID_88358 Human_SNP_ID_9787358 m1A Human chr1 - 37474623 37474623 37474623 CCCGCACCCTCCCCGCCGCGCCTCACCCCGCCATGCGCCAGCGGCGGCCGGCGGCGTCTCCATGG CCCGCACCCTCCCCGCCGCGCCTCACCCCGCCTTGCGCCAGCGGCGGCCGGCGGCGTCTCCATGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37474609..37474698 26863196 MeRIP-seq:(Medium) rs1046241212 Functional Loss SNV dbSNP153 33..33 33 - - - 88359 RMVar_ID_88359 Human_SNP_ID_9787364 m1A Human chr1 - 37474631 37474631 37474631 CGCCGAGGCCCGCACCCTCCCCGCCGCGCCTCACCCCGCCATGCGCCAGCGGCGGCCGGCGGCGT CGCCGAGGCCCGCACCCTCCCCGCCGCGCCTCCCCCCGCCATGCGCCAGCGGCGGCCGGCGGCGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37474595..37474714 26863196 MeRIP-seq:(Medium) rs995161223 Functional Loss SNV dbSNP153 33..33 33 - - - 88360 RMVar_ID_88360 Human_SNP_ID_9787365 m1A Human chr1 + 37474633 37474633 37474633 GCCGCCGGCCGCCGCTGGCGCATGGCGGGGTGAGGCGCGGCGGGGAGGGTGCGGGCCTCGGCGGG GCCGCCGGCCGCCGCTGGCGCATGGCGGGGTGGGGCGCGGCGGGGAGGGTGCGGGCCTCGGCGGG A G ZC3H12A Ensembl:ENSG00000163874 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:37474607..37474713 26863196 MeRIP-seq:(Medium) rs879382577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19037695,Human_RBP_ID_26774266 88361 RMVar_ID_88361 Human_SNP_ID_9787627 m1A Human chr1 + 37475536 37475536 37475536 GCCCCTGTGGAGAGAAGCCTGTCCTGGAAGCCAGCCCCACCATGAGTCTGTGGGAATTTGAGGAC GCCCCTGTGGAGAGAAGCCTGTCCTGGAAGCCGGCCCCACCATGAGTCTGTGGGAATTTGAGGAC A G ZC3H12A Ensembl:ENSG00000163874 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37475487..37475574 26863196 MeRIP-seq:(Medium) rs1378832504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_48462,Human_Splice_Rec_48472 RMVar_hsa_circ_27759 88362 RMVar_ID_88362 Human_SNP_ID_9788820 m1A Human chr1 + 37480423 37480423 37480423 GGAGGAAGGAGCAGCCTCGGCCCGACGTGCCCATCACAGGTGAGTGGTGCCTCTGGAGGTGGGAT GGAGGAAGGAGCAGCCTCGGCCCGACGTGCCCGTCACAGGTGAGTGGTGCCTCTGGAGGTGGGAT A G ZC3H12A Ensembl:ENSG00000163874 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37480372..37480486 26863196 MeRIP-seq:(Medium) rs1322777851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_852532,Human_RBP_ID_19037698 Human_Splice_Rec_48465,Human_Splice_Rec_48475,Human_Splice_Rec_48481 88363 RMVar_ID_88363 Human_SNP_ID_9789092 m1A Human chr1 - 37481654 37481654 37481654 GCACACCACCCGCTTGCCACCCACGCGTCGTGATGGTGTGAACACCAGGATCTTCTTCTTCTCCA GCACACCACCCGCTTGCCACCCACGCGTCGTGCTGGTGTGAACACCAGGATCTTCTTCTTCTCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37481594..37481714 26863196 MeRIP-seq:(Medium) rs1460740431 Functional Loss SNV dbSNP153 33..33 33 - - - 88364 RMVar_ID_88364 Human_SNP_ID_9789671 m1A Human chr1 + 37483300 37483300 37483300 CCTTTGGCCGGGCCATGGGTGCTGGCCACTTCAGTGTCCCTGCCGACTACCCACCCGCGCCCCCT CCTTTGGCCGGGCCATGGGTGCTGGCCACTTCGGTGTCCCTGCCGACTACCCACCCGCGCCCCCT A G ZC3H12A Ensembl:ENSG00000163874 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37483254..37483461 26863196 MeRIP-seq:(Medium) rs753678927 Functional Loss SNV dbSNP153 33..33 33 - - - 88365 RMVar_ID_88365 Human_SNP_ID_9797880 m1A Human chr1 - 37514410 37514410 37514410 GCGGGAGGGGGAGGGGAAGCGGCAGCCGCAGGAGGGGGCGTGGAGGGAGGACGGTGCCGGGGCCC GCGGGAGGGGGAGGGGAAGCGGCAGCCGCAGGTGGGGGCGTGGAGGGAGGACGGTGCCGGGGCCC T A MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37514406..37514499 26863196 MeRIP-seq:(Medium) rs1303033790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8166990 88366 RMVar_ID_88366 Human_SNP_ID_9798004 m1A Human chr1 - 37514730 37514730 37514730 CCCGCCTCAGCCCAACATGGCGATGCACAACAAGGCGGCGCCGCCGCAGATCCCGGACACCCGGC CCCGCCTCAGCCCAACATGGCGATGCACAACAGGGCGGCGCCGCCGCAGATCCCGGACACCCGGC T C MEAF6 Ensembl:ENSG00000163875 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:37514612..37514775 26863196 MeRIP-seq:(Medium) rs1465191726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4049735,Human_RBP_ID_5486250,Human_RBP_ID_26798169 Human_Splice_Rec_48485,Human_Splice_Rec_48499,Human_Splice_Rec_48521,Human_Splice_Rec_48535,Human_Splice_Rec_48551,Human_Splice_Rec_48575 88367 RMVar_ID_88367 Human_SNP_ID_9798005 m1A Human chr1 - 37514731 37514731 37514731 GCCCGCCTCAGCCCAACATGGCGATGCACAACAAGGCGGCGCCGCCGCAGATCCCGGACACCCGG GCCCGCCTCAGCCCAACATGGCGATGCACAACTAGGCGGCGCCGCCGCAGATCCCGGACACCCGG T A MEAF6 Ensembl:ENSG00000163875 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37514604..37514775 26863196 MeRIP-seq:(Medium) rs779682838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4049735,Human_RBP_ID_5486250,Human_RBP_ID_26798169 Human_Splice_Rec_48485,Human_Splice_Rec_48499,Human_Splice_Rec_48521,Human_Splice_Rec_48535,Human_Splice_Rec_48551,Human_Splice_Rec_48575 88368 RMVar_ID_88368 Human_SNP_ID_9808191 m1A Human chr1 + 37552690 37552690 37552690 ACTGTTGAGTGGTGAGGACTTCGGTTTCTCTTACTGCGAGGAGACTTGCTTCTTCTCCCTGAGGC ACTGTTGAGTGGTGAGGACTTCGGTTTCTCTTGCTGCGAGGAGACTTGCTTCTTCTCCCTGAGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37552589..37554046 26863196 MeRIP-seq:(Medium) rs867611845 Functional Loss SNV dbSNP153 33..33 33 - - - 88369 RMVar_ID_88369 Human_SNP_ID_9808194 m1A Human chr1 + 37552696 37552694 37552697 GAGTGGTGAGGACTTCGGTTTCTCTTACTGCGAGGAGACTTGCTTCTTCTCCCTGAGGCCTTGTT GAGTGGTGAGGACTTCGGTTTCTCTTACTGC___GAGACTTGCTTCTTCTCCCTGAGGCCTTGTT CGAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37552590..37554245 26863196 MeRIP-seq:(Medium) rs781322194 Functional Loss DEL dbSNP153 32..34 33 - - - 88370 RMVar_ID_88370 Human_SNP_ID_9808630 m1A Human chr1 - 37554214 37554214 37554214 CCAGCCAAAATCACAGAATGAAGGCGGTGAAGAGCGAACGGGAGCGAGGGAGCCGGCGAAGACAC CCAGCCAAAATCACAGAATGAAGGCGGTGAAGGGCGAACGGGAGCGAGGGAGCCGGCGAAGACAC T C SNIP1 Ensembl:ENSG00000163877 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:37554164..37554235 26863196 MeRIP-seq:(Medium) rs1443545868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8228270,Human_RBP_ID_9356061,Human_RBP_ID_18968023,Human_RBP_ID_22784865,Human_RBP_ID_26310895 88371 RMVar_ID_88371 Human_SNP_ID_9811961 m1A Human chr1 - 37567763 37567763 37567763 AAATTCCTGTTTGTGTATTGTTTGTATCCAGCACCTTCCAAAAAGGGAAAGAAGCGGAAGGCACA AAATTCCTGTTTGTGTATTGTTTGTATCCAGCGCCTTCCAAAAAGGGAAAGAAGCGGAAGGCACA T C GNL2 Ensembl:ENSG00000134697 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:37567651..37567775 26863196 MeRIP-seq:(Medium) rs1303394089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190336,Human_RBP_ID_24541089,Human_RBP_ID_26310899 Human_Splice_Rec_48645,Human_Splice_Rec_48674,Human_Splice_Rec_48675,Human_Splice_Rec_48680,Human_Splice_Rec_48681,Human_Splice_Rec_48684,Human_Splice_Rec_48685 88372 RMVar_ID_88372 Human_SNP_ID_9813529 m1A Human chr1 - 37574393 37574393 37574393 AGATGGTCCTCAATGACTGGCAGAGGGGCCGGATTCCTTTCTTTGTCAAGCCACCCAATGCAGAG AGATGGTCCTCAATGACTGGCAGAGGGGCCGGTTTCCTTTCTTTGTCAAGCCACCCAATGCAGAG T A GNL2 Ensembl:ENSG00000134697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37574326..37575598 32194978 MeRIP-seq:(Medium) rs762171160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742856,Human_RBP_ID_978087,Human_RBP_ID_5820127,Human_RBP_ID_8310333,Human_RBP_ID_9356067,Human_RBP_ID_22427133 Human_Splice_Rec_48668,Human_Splice_Rec_48669 RMVar_hsa_circ_55466,RMVar_hsa_circ_347576,RMVar_hsa_circ_131732,RMVar_hsa_circ_370785,RMVar_hsa_circ_361495,RMVar_hsa_circ_324515,RMVar_hsa_circ_131734,RMVar_hsa_circ_339516,RMVar_hsa_circ_131733,RMVar_hsa_circ_332079 88373 RMVar_ID_88373 Human_SNP_ID_9813530 m1A Human chr1 - 37574393 37574393 37574393 AGATGGTCCTCAATGACTGGCAGAGGGGCCGGATTCCTTTCTTTGTCAAGCCACCCAATGCAGAG AGATGGTCCTCAATGACTGGCAGAGGGGCCGGGTTCCTTTCTTTGTCAAGCCACCCAATGCAGAG T C GNL2 Ensembl:ENSG00000134697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37574326..37575598 32194978 MeRIP-seq:(Medium) rs762171160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742856,Human_RBP_ID_978087,Human_RBP_ID_5820127,Human_RBP_ID_8310333,Human_RBP_ID_9356067,Human_RBP_ID_22427133 Human_Splice_Rec_48668,Human_Splice_Rec_48669 RMVar_hsa_circ_55466,RMVar_hsa_circ_347576,RMVar_hsa_circ_131732,RMVar_hsa_circ_370785,RMVar_hsa_circ_361495,RMVar_hsa_circ_324515,RMVar_hsa_circ_131734,RMVar_hsa_circ_339516,RMVar_hsa_circ_131733,RMVar_hsa_circ_332079 88374 RMVar_ID_88374 Human_SNP_ID_9818081 m1A Human chr1 - 37592740 37592740 37592740 TATCAATCAACGGTGGCTTCTGGCACAGTGGCAAGAGTAGAGCCAAATATTAAATGGTTTGGTGA TATCAATCAACGGTGGCTTCTGGCACAGTGGCCAGAGTAGAGCCAAATATTAAATGGTTTGGTGA T G GNL2 Ensembl:ENSG00000134697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37590825..37593520 32194978 MeRIP-seq:(Medium) rs764777494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1348451,Human_RBP_ID_1430982,Human_RBP_ID_17762533 Human_Splice_Rec_48650,Human_Splice_Rec_48651,Human_Splice_Rec_48702,Human_Splice_Rec_48703 RMVar_hsa_circ_56579,RMVar_hsa_circ_50745,RMVar_hsa_circ_131738,RMVar_hsa_circ_107846,RMVar_hsa_circ_32408 88375 RMVar_ID_88375 Human_SNP_ID_9818822 m1A Human chr1 - 37595786 37595786 37595786 TGAAGCCCAAGTACAAAGGACGGAGCACCATCAACCCGTCCAAGGCCAGCACAAACCCAGGTACA TGAAGCCCAAGTACAAAGGACGGAGCACCATCTACCCGTCCAAGGCCAGCACAAACCCAGGTACA T A GNL2 Ensembl:ENSG00000134697 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:37595776..37595885 32194978 MeRIP-seq:(Medium) rs919303552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073883,Human_RBP_ID_5136202,Human_RBP_ID_22430454,Human_RBP_ID_26798174 Human_Splice_Rec_48647,Human_Splice_Rec_48705 88376 RMVar_ID_88376 Human_SNP_ID_9818823 m1A Human chr1 - 37595786 37595786 37595786 TGAAGCCCAAGTACAAAGGACGGAGCACCATCAACCCGTCCAAGGCCAGCACAAACCCAGGTACA TGAAGCCCAAGTACAAAGGACGGAGCACCATCGACCCGTCCAAGGCCAGCACAAACCCAGGTACA T C GNL2 Ensembl:ENSG00000134697 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:37595776..37595885 32194978 MeRIP-seq:(Medium) rs919303552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073883,Human_RBP_ID_5136202,Human_RBP_ID_22430454,Human_RBP_ID_26798174 Human_Splice_Rec_48647,Human_Splice_Rec_48705 88377 RMVar_ID_88377 Human_SNP_ID_9818866 m1A Human chr1 - 37595880 37595878 37595880 GCGGGTGTCTTCGGCCGGGCTTGGGAACATAAAAGTTTGTTTCACCACGTAAGCCGGACCTCGCA GCGGGTGTCTTCGGCCGGGCTTGGGAACATAA__GTTTGTTTCACCACGTAAGCCGGACCTCGCA CTT C GNL2 Ensembl:ENSG00000134697 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:37595797..37595925;chr1:37595751..37595925 26863196 MeRIP-seq:(Medium) rs1356186144 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_273433,Human_RBP_ID_978096,Human_RBP_ID_4049873,Human_RBP_ID_5136202,Human_RBP_ID_5458488,Human_RBP_ID_8753857,Human_RBP_ID_9270073,Human_RBP_ID_26798175 88378 RMVar_ID_88378 Human_SNP_ID_9841990 m1A Human chr1 - 37690027 37690026 37690027 GGGCGACAGTGAGACTCCGTCTCGAAAAAAAAACAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC GGGCGACAGTGAGACTCCGTCTCGAAAAAAAA_CAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC GT G C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1246787824 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17763606 Human_Splice_Rec_48799,Human_Splice_Rec_48807 88379 RMVar_ID_88379 Human_SNP_ID_9841992 m1A Human chr1 - 37690027 37690027 37690027 GGGCGACAGTGAGACTCCGTCTCGAAAAAAAAACAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC GGGCGACAGTGAGACTCCGTCTCGAAAAAAAATCAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC T A C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4653319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17763606 Human_Splice_Rec_48799,Human_Splice_Rec_48807 88380 RMVar_ID_88380 Human_SNP_ID_9841993 m1A Human chr1 - 37690027 37690027 37690027 GGGCGACAGTGAGACTCCGTCTCGAAAAAAAAACAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC GGGCGACAGTGAGACTCCGTCTCGAAAAAAAACCAAAAAAAAAACCCTGCTTCTGGAGGTGAGAC T G C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4653319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17763606 Human_Splice_Rec_48799,Human_Splice_Rec_48807 88381 RMVar_ID_88381 Human_SNP_ID_9842687 m1A Human chr1 + 37692557 37692557 37692557 CTCTCTCTCACTGGCACAGCGAGGTTTTGCTCAGCCCTTGTCTCGGGACCGCAGGTACGTGCCTG CTCTCTCTCACTGGCACAGCGAGGTTTTGCTCGGCCCTTGTCTCGGGACCGCAGGTACGTGCCTG A G CDCA8 Ensembl:ENSG00000134690 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:37692501..37692750 26863196 MeRIP-seq:(Medium) rs1304633992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1431030,Human_RBP_ID_4073888,Human_RBP_ID_22143058,Human_RBP_ID_22430456 Human_Splice_Rec_48813 88382 RMVar_ID_88382 Human_SNP_ID_9842693 m1A Human chr1 - 37692567 37692567 37692567 AAGAAGTCGCCAGGCACGTACCTGCGGTCCCGAGACAAGGGCTGAGCAAAACCTCGCTGTGCCAG AAGAAGTCGCCAGGCACGTACCTGCGGTCCCGGGACAAGGGCTGAGCAAAACCTCGCTGTGCCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37692519..37692664 26863196 MeRIP-seq:(Medium) rs1360866428 Functional Loss SNV dbSNP153 33..33 33 - - - 88383 RMVar_ID_88383 Human_SNP_ID_9842714 m1A Human chr1 - 37692607 37692607 37692607 AAACTGGGTAGGGACGAGGAGGGCGGACGGGGACCACCCGAAGAAGTCGCCAGGCACGTACCTGC AAACTGGGTAGGGACGAGGAGGGCGGACGGGGTCCACCCGAAGAAGTCGCCAGGCACGTACCTGC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:37692568..37692745 26863196 MeRIP-seq:(Medium) rs1233917274 Functional Loss SNV dbSNP153 33..33 33 - - - 88384 RMVar_ID_88384 Human_SNP_ID_9842721 m1A Human chr1 - 37692637 37692637 37692637 GGAGCGGCGGAGATGGGGCAGGGAAGCAAGAAACTGGGTAGGGACGAGGAGGGCGGACGGGGACC GGAGCGGCGGAGATGGGGCAGGGAAGCAAGAAGCTGGGTAGGGACGAGGAGGGCGGACGGGGACC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:37692501..37692933 26863410 MeRIP-seq:(Medium) rs1292143386 Functional Loss SNV dbSNP153 33..33 33 - - - 88385 RMVar_ID_88385 Human_SNP_ID_9845770 m1A Human chr1 - 37705456 37705456 37705456 ATCCGCTCTCCTGCTGCTGGAGTACGCAGGCCAGGGGTCTTGAAGACCCTAGAATGGGAAAATCT ATCCGCTCTCCTGCTGCTGGAGTACGCAGGCCGGGGGTCTTGAAGACCCTAGAATGGGAAAATCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37705451..37705575 32194978 MeRIP-seq:(Medium) rs1200283013 Functional Loss SNV dbSNP153 33..33 33 - - - 88386 RMVar_ID_88386 Human_SNP_ID_9846099 m1A Human chr1 + 37706502 37706502 37706502 GGGCCTGCCCTTAGAAAGCAGCTCAGTGGTCAAGATGGGTTTGCAATCATGGTACCTGTGATATG GGGCCTGCCCTTAGAAAGCAGCTCAGTGGTCAGGATGGGTTTGCAATCATGGTACCTGTGATATG A G CDCA8 Ensembl:ENSG00000134690 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37706497..37706573 26863196 MeRIP-seq:(Medium) rs919236868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121550,RMVar_hsa_circ_80312,RMVar_hsa_circ_131743,RMVar_hsa_circ_99251,RMVar_hsa_circ_11779,RMVar_hsa_circ_131745,RMVar_hsa_circ_131747 88387 RMVar_ID_88387 Human_SNP_ID_9846235 m1A Human chr1 + 37707056 37707056 37707056 AGCTGGATCCAGAGGCCTTGGGAAACATTAAGAAGCTCTCCGTAAGTCTCATATTCATCTCCACA AGCTGGATCCAGAGGCCTTGGGAAACATTAAGCAGCTCTCCGTAAGTCTCATATTCATCTCCACA A C CDCA8 Ensembl:ENSG00000134690 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37706976..37707075 32194978 MeRIP-seq:(Medium) rs560264444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5331460,Human_RBP_ID_19037721 Human_Splice_Rec_48830,Human_Splice_Rec_48831,Human_Splice_Rec_48848,Human_Splice_Rec_48849 RMVar_hsa_circ_121550,RMVar_hsa_circ_80312,RMVar_hsa_circ_131743,RMVar_hsa_circ_99251,RMVar_hsa_circ_11779,RMVar_hsa_circ_131745,RMVar_hsa_circ_131747 88388 RMVar_ID_88388 Human_SNP_ID_9868212 m1A Human chr1 + 37794165 37794165 37794165 CGCGGCACGCTGGGAGGTAGCGCGGCGGCTGCAGGAGCGCACAGTCGGCCATGGCCCGGCGGCGG CGCGGCACGCTGGGAGGTAGCGCGGCGGCTGCTGGAGCGCACAGTCGGCCATGGCCCGGCGGCGG A T MANEAL Ensembl:ENSG00000185090 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37794116..37794282 26863196 MeRIP-seq:(Medium) rs1471174866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072714,Human_RBP_ID_22428275,Human_RBP_ID_26753776 88389 RMVar_ID_88389 Human_SNP_ID_9872401 m1A Human chr1 + 37808580 37808580 37808580 ACCGCGGGAAGGCGGGGCTGGGGCTCGGCGGGAGGCCACCCCCACAGCCGCCCCGGGAGGAGCGC ACCGCGGGAAGGCGGGGCTGGGGCTCGGCGGGGGGCCACCCCCACAGCCGCCCCGGGAGGAGCGC A G C1orf122 Ensembl:ENSG00000197982 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:37808465..37808626 26863196 MeRIP-seq:(Medium) rs960368889 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4073895,Human_RBP_ID_8939968,Human_RBP_ID_9358639,Human_RBP_ID_22428279 Human_Splice_Rec_49080,Human_Splice_Rec_49082,Human_Splice_Rec_49086 RMVar_hsa_circ_82401,RMVar_hsa_circ_80254,RMVar_hsa_circ_131749,RMVar_hsa_circ_131750 88390 RMVar_ID_88390 Human_SNP_ID_9872459 m1A Human chr1 - 37808734 37808734 37808734 CCCCACCCCAGCCCAGCCCAGGGTGGGCACTAACCCCGCCACCAGCCGGCTCCGGGCGCCGGCGG CCCCACCCCAGCCCAGCCCAGGGTGGGCACTACCCCCGCCACCAGCCGGCTCCGGGCGCCGGCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:37808726..37808750 26863196 MeRIP-seq:(Medium) rs979650900 Functional Loss SNV dbSNP153 33..33 33 - - - 88391 RMVar_ID_88391 Human_SNP_ID_9872584 m1A Human chr1 + 37809041 37809041 37809041 AGCCGGCTGTCTCCGCCAGAGGCGGCTTTCCAAAGGATGCTGGCGATGGAGCTGCGGAGCCCTGA AGCCGGCTGTCTCCGCCAGAGGCGGCTTTCCAGAGGATGCTGGCGATGGAGCTGCGGAGCCCTGA A G C1orf122 Ensembl:ENSG00000197982 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:37808564..37809075 32194978 MeRIP-seq:(Medium) rs61745801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354596,Human_RBP_ID_1255560,Human_RBP_ID_1747337,Human_RBP_ID_4050351,Human_RBP_ID_8310448,Human_RBP_ID_18574188,Human_RBP_ID_22871594 Human_Splice_Rec_49078,Human_Splice_Rec_49084,Human_Splice_Rec_49088 Human_miRNA_ID_2440080 RMVar_hsa_circ_110521,RMVar_hsa_circ_82401,RMVar_hsa_circ_80254,RMVar_hsa_circ_131749,RMVar_hsa_circ_131750,RMVar_hsa_circ_131751 88392 RMVar_ID_88392 Human_SNP_ID_9884895 m1A Human chr1 - 37861056 37861056 37861056 GGGAGACTGAGGTGGGAGCATCACTTGAGACCAGGAGTTTGGGACCAGGCTGGGCAACACAGGGA GGGAGACTGAGGTGGGAGCATCACTTGAGACCGGGAGTTTGGGACCAGGCTGGGCAACACAGGGA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1136981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385951 88393 RMVar_ID_88393 Human_SNP_ID_9888320 m1A Human chr1 - 37874122 37874122 37874122 TCTGTTTTCAGAATGTGAAGTACATGCAATTGAAAGTAGAATCCTTTACAATTCATAATGGACAA TCTGTTTTCAGAATGTGAAGTACATGCAATTGGAAGTAGAATCCTTTACAATTCATAATGGACAA T C INPP5B Ensembl:ENSG00000204084 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37874074..37874201 32194978 MeRIP-seq:(Medium) rs768968308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2146229,Human_RBP_ID_10973062,Human_RBP_ID_23392842 Human_Splice_Rec_49134,Human_Splice_Rec_49176,Human_Splice_Rec_49210,Human_Splice_Rec_49254,Human_Splice_Rec_49296 RMVar_hsa_circ_131759,RMVar_hsa_circ_90742,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_265083,RMVar_hsa_circ_265710,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_352889,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_311918 88394 RMVar_ID_88394 Human_SNP_ID_9897241 m1A Human chr1 - 37909329 37909329 37909329 GAAGAAGAGTTGGGAGCTGGCTCGGCCTGGCAAGGAGCAGCCTGGGGAGGAGGGTAGAGGTCAGA GAAGAAGAGTTGGGAGCTGGCTCGGCCTGGCACGGAGCAGCCTGGGGAGGAGGGTAGAGGTCAGA T G INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37909196..37909524 26863196 MeRIP-seq:(Medium) rs556714923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_343429,RMVar_hsa_circ_265711,RMVar_hsa_circ_81814,RMVar_hsa_circ_131764,RMVar_hsa_circ_347455,RMVar_hsa_circ_36098,RMVar_hsa_circ_84168,RMVar_hsa_circ_131768,RMVar_hsa_circ_82193,RMVar_hsa_circ_131771,RMVar_hsa_circ_267156 88395 RMVar_ID_88395 Human_SNP_ID_9897715 m1A Human chr1 + 37911249 37911249 37911249 CCATAACTTTCAAAATCTATTTTCCTCCTCACACTTGACGCATATACTTTCTGCCCCCCAGCTCT CCATAACTTTCAAAATCTATTTTCCTCCTCACGCTTGACGCATATACTTTCTGCCCCCCAGCTCT A G HSALNG0002670 RNACentral:URS0000E9B34E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37911247..37911329 26863196 MeRIP-seq:(Medium) rs889559413 Functional Loss SNV dbSNP153 33..33 33 - - - 88396 RMVar_ID_88396 Human_SNP_ID_9906748 m1A Human chr1 + 37946218 37946218 37946218 ACACCTTCCATTCCTCTTCCCAAGGCCAGGGCAGGCTCAGGGCCGCAGTTAGCACAGGAAGGATA ACACCTTCCATTCCTCTTCCCAAGGCCAGGGCGGGCTCAGGGCCGCAGTTAGCACAGGAAGGATA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37946215..37946329 26863196 MeRIP-seq:(Medium) rs772713932 Functional Loss SNV dbSNP153 33..33 33 - - - 88397 RMVar_ID_88397 Human_SNP_ID_9909272 m1A Human chr1 - 37957116 37957116 37957116 ATGTGGTGTCTGAAATGGAAAGAACTAAGGCAACCAGGAAGGCACTGATCTGCCTTATAAGCACA ATGTGGTGTCTGAAATGGAAAGAACTAAGGCAGCCAGGAAGGCACTGATCTGCCTTATAAGCACA T C SF3A3 Ensembl:ENSG00000183431 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:37957067..37957176 26863196 MeRIP-seq:(Medium) rs1167288147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354629,Human_RBP_ID_1431142,Human_RBP_ID_1747367,Human_RBP_ID_10973634,Human_RBP_ID_18230176,Human_RBP_ID_23205106,Human_RBP_ID_26385960 88398 RMVar_ID_88398 Human_SNP_ID_9920317 m1A Human chr1 + 37997173 37997173 37997173 ACCCAGACTGCAGGGGAGAGGGTGAATTCTGGAGTCCAGGTGTGGGGAGGGGGCTTGACTCATGG ACCCAGACTGCAGGGGAGAGGGTGAATTCTGGGGTCCAGGTGTGGGGAGGGGGCTTGACTCATGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37997124..37997293 26863196 MeRIP-seq:(Medium) rs1333459115 Functional Loss SNV dbSNP153 33..33 33 - - - 88399 RMVar_ID_88399 Human_SNP_ID_9921119 m1A Human chr1 + 37999419 37999419 37999419 TTTGCACAGTCAAATGACTCGCTCATGGTGGCAAGGGGAGAGAACCCTGTTAGGAGCACAAGGTG TTTGCACAGTCAAATGACTCGCTCATGGTGGCGAGGGGAGAGAACCCTGTTAGGAGCACAAGGTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:37999368..37999533 26863196 MeRIP-seq:(Medium) rs575378257 Functional Loss SNV dbSNP153 33..33 33 - - - 88400 RMVar_ID_88400 Human_SNP_ID_9926018 m1A Human chr1 - 38017755 38017755 38017755 AGCCATTGGGCACCCACCTGGAGTTTAACCCGAGTCATTTTGTAGTAGAATTCATCTGGATTTTT AGCCATTGGGCACCCACCTGGAGTTTAACCCGCGTCATTTTGTAGTAGAATTCATCTGGATTTTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:38017707..38018551 32194978 MeRIP-seq:(Medium) rs772300011 Functional Loss SNV dbSNP153 33..33 33 - - - 88401 RMVar_ID_88401 Human_SNP_ID_10121936 m1A Human chr1 - 38859675 38859673 38859675 CGGCGGCCTGGCTCGGCCTGGCCTGGCCTGTCAGGGCGCGGGCGGCGGCGGCTCCAGCACCATGT CGGCGGCCTGGCTCGGCCTGGCCTGGCCTGTC__GGCGCGGGCGGCGGCGGCTCCAGCACCATGT CCT C AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:38859574..38859724 26863410 MeRIP-seq:(Medium) rs1557589919 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4050700,Human_RBP_ID_9318853 88402 RMVar_ID_88402 Human_SNP_ID_10121937 m1A Human chr1 - 38859675 38859675 38859675 CGGCGGCCTGGCTCGGCCTGGCCTGGCCTGTCAGGGCGCGGGCGGCGGCGGCTCCAGCACCATGT CGGCGGCCTGGCTCGGCCTGGCCTGGCCTGTCGGGGCGCGGGCGGCGGCGGCTCCAGCACCATGT T C AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:38859574..38859724 26863410 MeRIP-seq:(Medium) rs1355502526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4050700,Human_RBP_ID_9318853 88403 RMVar_ID_88403 Human_SNP_ID_10121954 m1A Human chr1 + 38859695 38859690 38859695 CCGCCCGCGCCCTGACAGGCCAGGCCAGGCCGAGCCAGGCCGCCGCCTCCCCAGTCCGCCTCCGC CCGCCCGCGCCCTGACAGGCCAGGCCAG_____GCCAGGCCGCCGCCTCCCCAGTCCGCCTCCGC GGCCGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:38857048..38859773 26863196 MeRIP-seq:(Medium) rs1180547908 Functional Loss DEL dbSNP153 29..33 33 - - - 88404 RMVar_ID_88404 Human_SNP_ID_10121959 m1A Human chr1 + 38859695 38859695 38859695 CCGCCCGCGCCCTGACAGGCCAGGCCAGGCCGAGCCAGGCCGCCGCCTCCCCAGTCCGCCTCCGC CCGCCCGCGCCCTGACAGGCCAGGCCAGGCCGGGCCAGGCCGCCGCCTCCCCAGTCCGCCTCCGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:38857048..38859773 26863196 MeRIP-seq:(Medium) rs1352670249 Functional Loss SNV dbSNP153 33..33 33 - - - 88405 RMVar_ID_88405 Human_SNP_ID_10121973 m1A Human chr1 - 38859710 38859710 38859710 GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGAGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGTGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG T A AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:38856935..38864638 26863196 MeRIP-seq:(Medium) rs983372405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223349,Human_RBP_ID_744821,Human_RBP_ID_801415,Human_RBP_ID_3334955,Human_RBP_ID_4073900,Human_RBP_ID_5161564,Human_RBP_ID_9318853,Human_RBP_ID_22469325 88406 RMVar_ID_88406 Human_SNP_ID_10121974 m1A Human chr1 - 38859710 38859710 38859710 GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGAGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGGGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG T C AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:38856935..38864638 26863196 MeRIP-seq:(Medium) rs983372405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223349,Human_RBP_ID_744821,Human_RBP_ID_801415,Human_RBP_ID_3334955,Human_RBP_ID_4073900,Human_RBP_ID_5161564,Human_RBP_ID_9318853,Human_RBP_ID_22469325 88407 RMVar_ID_88407 Human_SNP_ID_10121975 m1A Human chr1 - 38859710 38859710 38859710 GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGAGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG GTGGTGGCGGCGGCGGCGGAGGCGGACTGGGGCGGCGGCGGCCTGGCTCGGCCTGGCCTGGCCTG T G AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:38856935..38864638 26863196 MeRIP-seq:(Medium) rs983372405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223349,Human_RBP_ID_744821,Human_RBP_ID_801415,Human_RBP_ID_3334955,Human_RBP_ID_4073900,Human_RBP_ID_5161564,Human_RBP_ID_9318853,Human_RBP_ID_22469325 88408 RMVar_ID_88408 Human_SNP_ID_10123025 m1A Human chr1 + 38863704 38863702 38863705 TGTATTAATATCAGTCTTTGGCCTAAAAATTCAGCACCCCTCTTCCCCTTATACTTGTCCCACCT TGTATTAATATCAGTCTTTGGCCTAAAAATT___CACCCCTCTTCCCCTTATACTTGTCCCACCT TCAG T AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:38863660..38863761 32194978 MeRIP-seq:(Medium) rs978726557 Functional Loss DEL dbSNP153 32..34 33 - - - 88409 RMVar_ID_88409 Human_SNP_ID_10125607 m1A Human chr1 + 38873231 38873229 38873231 CCAAACCTGCGCGCGCGACCCCACTCCCACCCAGAGCCGACCAGCGGCTTGCTACCGCCCGCATG CCAAACCTGCGCGCGCGACCCCACTCCCACC__GAGCCGACCAGCGGCTTGCTACCGCCCGCATG CCA C AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:38873229..38873336 26863196 MeRIP-seq:(Medium) rs968531183 Functional Loss DEL dbSNP153 32..33 33 - - - 88410 RMVar_ID_88410 Human_SNP_ID_10156806 m1A Human chr1 + 38991556 38991553 38991556 GTTTCAGACGCAGACCCCACCGCAGAGTCTGCAGCAGCCCGCCCCGCCCGGCAGCGAGCGGCGCC GTTTCAGACGCAGACCCCACCGCAGAGTCT___GCAGCCCGCCCCGCCCGGCAGCGAGCGGCGCC TGCA T AKIRIN1 Ensembl:ENSG00000174574 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:38991298..38991580 26863196 MeRIP-seq:(Medium) rs1272583807 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_22428280,Human_RBP_ID_22532113 Human_Splice_Rec_49777,Human_Splice_Rec_49785,Human_Splice_Rec_49791,Human_Splice_Rec_49797 88411 RMVar_ID_88411 Human_SNP_ID_10167329 m1A Human chr1 + 39028795 39028795 39028795 CATAGATCGATGGTTGACAATCCAGAGTGGTGAACAGCCCTACAAGATGGCTGGTCGATGCCATG CATAGATCGATGGTTGACAATCCAGAGTGGTGCACAGCCCTACAAGATGGCTGGTCGATGCCATG A C NDUFS5 Ensembl:ENSG00000168653 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs773573777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354868,Human_RBP_ID_1431266,Human_RBP_ID_1747515,Human_RBP_ID_4095503,Human_RBP_ID_8969864,Human_RBP_ID_10977384,Human_RBP_ID_22749049,Human_RBP_ID_23393366 Human_Splice_Rec_49804,Human_Splice_Rec_49808 Human_miRNA_ID_2170638 RMVar_hsa_circ_131808,RMVar_hsa_circ_328575,RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 88412 RMVar_ID_88412 Human_SNP_ID_10168337 m1A Human chr1 + 39032650 39032650 39032650 AGAGTCAGTGAGCTTATGCTATAGTGGGAGGAAGAGCAGAAAAATAACAAGTAAAAATACAGGTG AGAGTCAGTGAGCTTATGCTATAGTGGGAGGAGGAGCAGAAAAATAACAAGTAAAAATACAGGTG A G NDUFS5 Ensembl:ENSG00000168653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39032647..39032832 26863196 MeRIP-seq:(Medium) rs57575779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 88413 RMVar_ID_88413 Human_SNP_ID_10168796 m1A Human chr1 + 39034526 39034526 39034526 TGAACAGAGCAGCTGCTGATGTCTGGAGGCTGATTTTCCTGTTCTCTGTTCTCCACTGGAAAGGT TGAACAGAGCAGCTGCTGATGTCTGGAGGCTGGTTTTCCTGTTCTCTGTTCTCCACTGGAAAGGT A G NDUFS5 Ensembl:ENSG00000168653 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:39034476..39034550 32194978 MeRIP-seq:(Medium) rs1358768015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354874,Human_RBP_ID_24452702 RMVar_hsa_circ_113812,RMVar_hsa_circ_131809,RMVar_hsa_circ_131807 88414 RMVar_ID_88414 Human_SNP_ID_10189796 m1A Human chr1 + 39115925 39115925 39115925 GGTCAAATAAGGCAAAGACTACAGATGTCCAAAATAAAGGTTACTGCTACTGGAACATTTTCAGT GGTCAAATAAGGCAAAGACTACAGATGTCCAACATAAAGGTTACTGCTACTGGAACATTTTCAGT A C MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:39115920..39116177 26863196 MeRIP-seq:(Medium) rs991250412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111267,RMVar_hsa_circ_131812,RMVar_hsa_circ_44906,RMVar_hsa_circ_120982,RMVar_hsa_circ_131811,RMVar_hsa_circ_348868,RMVar_hsa_circ_89287,RMVar_hsa_circ_131813 88415 RMVar_ID_88415 Human_SNP_ID_10189824 m1A Human chr1 + 39116063 39116063 39116063 GAGAGGAGGAAGACAGGTGAAGAAGGGTGGGGAGAGTTTTGTTTATGTATTGTAACACAGGAGAG GAGAGGAGGAAGACAGGTGAAGAAGGGTGGGGGGAGTTTTGTTTATGTATTGTAACACAGGAGAG A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39116055..39116145 26863196 MeRIP-seq:(Medium) rs551441144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803706 RMVar_hsa_circ_111267,RMVar_hsa_circ_131812,RMVar_hsa_circ_44906,RMVar_hsa_circ_120982,RMVar_hsa_circ_131811,RMVar_hsa_circ_348868,RMVar_hsa_circ_89287,RMVar_hsa_circ_131813 88416 RMVar_ID_88416 Human_SNP_ID_10232375 m1A Human chr1 - 39295146 39295146 39295146 GACCTTCACACATTCTCAAGTCACACACCTCCACTGTCTGCTTGGCTGGGTGGTTCTCAAGTGAA GACCTTCACACATTCTCAAGTCACACACCTCCGCTGTCTGCTTGGCTGGGTGGTTCTCAAGTGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39295096..39297670 32194978 MeRIP-seq:(Medium) rs1416656052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131848 88417 RMVar_ID_88417 Human_SNP_ID_10255455 m1A Human chr1 + 39385468 39385468 39385468 TATGCTAAAGGAATTTGAAGCACGCAGGCAACAGCATGAGCAACTGAATGAGGCAGCTCAGGGCA TATGCTAAAGGAATTTGAAGCACGCAGGCAACTGCATGAGCAACTGAATGAGGCAGCTCAGGGCA A T MACF1 Ensembl:ENSG00000127603 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39385445..39385746 32194978 MeRIP-seq:(Medium) rs764650719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_852561,Human_RBP_ID_1747568,Human_RBP_ID_5234478,Human_RBP_ID_5458307,Human_RBP_ID_5518861,Human_RBP_ID_9252911,Human_RBP_ID_26311017,Human_RBP_ID_27797892 Human_Splice_Rec_49932,Human_Splice_Rec_50130,Human_Splice_Rec_50312,Human_Splice_Rec_50646,Human_Splice_Rec_50856,Human_Splice_Rec_51224,Human_Splice_Rec_51352 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_126542,RMVar_hsa_circ_98617,RMVar_hsa_circ_131833,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_70111,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_59788,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_3809,RMVar_hsa_circ_51881,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_323102,RMVar_hsa_circ_131875,RMVar_hsa_circ_48984,RMVar_hsa_circ_311189,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_361308,RMVar_hsa_circ_4832,RMVar_hsa_circ_131907,RMVar_hsa_circ_351511,RMVar_hsa_circ_131910,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_50750,RMVar_hsa_circ_131913,RMVar_hsa_circ_58400,RMVar_hsa_circ_131915,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_64189,RMVar_hsa_circ_82012,RMVar_hsa_circ_49782,RMVar_hsa_circ_131919,RMVar_hsa_circ_131921,RMVar_hsa_circ_317413,RMVar_hsa_circ_131920,RMVar_hsa_circ_286087 88418 RMVar_ID_88418 Human_SNP_ID_10261510 m1A Human chr1 + 39409233 39409224 39409233 GCGGGCGGGGAGGACGGCGGGGCCGCGGGGCCAGCGGCGTGGTGGAGAATAGAGGCGGCTGCTTG GCGGGCGGGGAGGACGGCGGGGCC_________GCGGCGTGGTGGAGAATAGAGGCGGCTGCTTG CGCGGGGCCA C MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:39409053..39409484 26863196 MeRIP-seq:(Medium) rs1417606072 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_803731,Human_RBP_ID_4072728,Human_RBP_ID_5518878,Human_RBP_ID_21962366,Human_RBP_ID_22558765,Human_RBP_ID_22706652,Human_RBP_ID_24550354 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919 88419 RMVar_ID_88419 Human_SNP_ID_10261513 m1A Human chr1 + 39409233 39409233 39409233 GCGGGCGGGGAGGACGGCGGGGCCGCGGGGCCAGCGGCGTGGTGGAGAATAGAGGCGGCTGCTTG GCGGGCGGGGAGGACGGCGGGGCCGCGGGGCCCGCGGCGTGGTGGAGAATAGAGGCGGCTGCTTG A C MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:39409053..39409484 26863196 MeRIP-seq:(Medium) rs1393921354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803731,Human_RBP_ID_4072728,Human_RBP_ID_5518878,Human_RBP_ID_21962366,Human_RBP_ID_22558765,Human_RBP_ID_22706652,Human_RBP_ID_24550354 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919 88420 RMVar_ID_88420 Human_SNP_ID_10262559 m1A Human chr1 + 39412497 39412497 39412497 CAAGCTCCAGCACATTTCCACAGAAACTTCCCAGAGCAGGTCTTCCAGGATCTCCAGAGGAAGTC CAAGCTCCAGCACATTTCCACAGAAACTTCCCCGAGCAGGTCTTCCAGGATCTCCAGAGGAAGTC A C MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39412493..39412694 32194978 MeRIP-seq:(Medium) rs1032262079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4051429,Human_RBP_ID_22520254 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919 88421 RMVar_ID_88421 Human_SNP_ID_10262560 m1A Human chr1 + 39412497 39412497 39412497 CAAGCTCCAGCACATTTCCACAGAAACTTCCCAGAGCAGGTCTTCCAGGATCTCCAGAGGAAGTC CAAGCTCCAGCACATTTCCACAGAAACTTCCCGGAGCAGGTCTTCCAGGATCTCCAGAGGAAGTC A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39412493..39412694 32194978 MeRIP-seq:(Medium) rs1032262079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4051429,Human_RBP_ID_22520254 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919 88422 RMVar_ID_88422 Human_SNP_ID_10263103 m1A Human chr1 - 39413770 39413770 39413770 TGGGGTGGGCACTGCAGCAGCTGGGGAGGCAGATTCCTCGGGGGTGGGCACTGCAACAGCTGCGG TGGGGTGGGCACTGCAGCAGCTGGGGAGGCAGGTTCCTCGGGGGTGGGCACTGCAACAGCTGCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:39413735..39413824 26863196 MeRIP-seq:(Medium) rs1455812727 Functional Loss SNV dbSNP153 33..33 33 - - - 88423 RMVar_ID_88423 Human_SNP_ID_10263235 m1A Human chr1 + 39413997 39413995 39413998 GCAGTGTCCAACCCAGAGGAGCCCACCTCCCCAGCAGCAGCAGTGCCCACCCTAGAGGAACCCAC GCAGTGTCCAACCCAGAGGAGCCCACCTCCC___CAGCAGCAGTGCCCACCCTAGAGGAACCCAC CCAG C MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:39413751..39414225 26863196 MeRIP-seq:(Medium) rs755032342 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_96825,Human_RBP_ID_803737,Human_RBP_ID_860227,Human_RBP_ID_5518897,Human_RBP_ID_17071476 Human_miRNA_ID_1355259 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_131916,RMVar_hsa_circ_124316,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919 88424 RMVar_ID_88424 Human_SNP_ID_10263259 m1A Human chr1 - 39414081 39414043 39414082 GGGGAGGCAGGCTCCTCGGGGGTGGGCACTGAAGCTGCTGGGGAACTGAGTTCCTCTGGGGTGAG GGGGAGGCAGGCTCCTCGGGGGTGGGCACTG__________________________________ GCAGTGCTCACCCCAGAGGAACTCAGTTCCCCAGCAGCTT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:39413998..39414149 26863196 MeRIP-seq:(Medium) rs1394037119 Functional Loss DEL dbSNP153 32..65 33 - - - 88425 RMVar_ID_88425 Human_SNP_ID_10263278 m1A Human chr1 - 39414081 39414081 39414081 GGGGAGGCAGGCTCCTCGGGGGTGGGCACTGAAGCTGCTGGGGAACTGAGTTCCTCTGGGGTGAG GGGGAGGCAGGCTCCTCGGGGGTGGGCACTGAGGCTGCTGGGGAACTGAGTTCCTCTGGGGTGAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:39413998..39414149 26863196 MeRIP-seq:(Medium) rs760615615 Functional Loss SNV dbSNP153 33..33 33 - - - 88426 RMVar_ID_88426 Human_SNP_ID_10301070 m1A Human chr1 - 39563604 39563604 39563604 ATCCTGCCATACAGCCTCTGCAGGTGAGGTTCACCAGACAGAATGCTTAAAAGGATTTCCCCCAT ATCCTGCCATACAGCCTCTGCAGGTGAGGTTCGCCAGACAGAATGCTTAAAAGGATTTCCCCCAT T C PABPC4 Ensembl:ENSG00000090621 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:39563601..39563727 32194978 MeRIP-seq:(Medium) rs757048030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2183221,Human_RBP_ID_18968062,Human_RBP_ID_19034619 RMVar_hsa_circ_75969,RMVar_hsa_circ_116806,RMVar_hsa_circ_113357,RMVar_hsa_circ_31319,RMVar_hsa_circ_131960,RMVar_hsa_circ_131961,RMVar_hsa_circ_131959,RMVar_hsa_circ_26878 88427 RMVar_ID_88427 Human_SNP_ID_10301129 m1A Human chr1 + 39563718 39563718 39563718 AGCAGCAGCAGCAACAGCAGCGCGTGGCGCTAAGTTCTGCACAGCTGTGGGAACGCCTTAGGGAA AGCAGCAGCAGCAACAGCAGCGCGTGGCGCTAGGTTCTGCACAGCTGTGGGAACGCCTTAGGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:39563587..39563778 26863196 MeRIP-seq:(Medium) rs760010568 Functional Loss SNV dbSNP153 33..33 33 - - - 88428 RMVar_ID_88428 Human_SNP_ID_10304992 m1A Human chr1 + 39576075 39576075 39576075 CGCCGCGGCTCACAGGTGGCACCGGCGCGGCGAGGACGAGCTGGAGTCGGCGGGCTTGGAGACGG CGCCGCGGCTCACAGGTGGCACCGGCGCGGCGTGGACGAGCTGGAGTCGGCGGGCTTGGAGACGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:39575976..39576150 26863410 MeRIP-seq:(Medium) rs1465967629 Functional Loss SNV dbSNP153 33..33 33 - - - 88429 RMVar_ID_88429 Human_SNP_ID_10304998 m1A Human chr1 - 39576084 39576081 39576084 GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCCAGCTCGTCCTCGCCGCGCCGGTGCCACCTGTGA GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCC___TCGTCCTCGCCGCGCCGGTGCCACCTGTGA AGCT A PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39575991..39576092 32194978 MeRIP-seq:(Medium) rs1204210098 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_24260,Human_RBP_ID_354974,Human_RBP_ID_4095795,Human_RBP_ID_8753921,Human_RBP_ID_9319943,Human_RBP_ID_9358702,Human_RBP_ID_18574693,Human_RBP_ID_22023246,Human_RBP_ID_22488139,Human_RBP_ID_26798219,Human_RBP_ID_26864553,Human_RBP_ID_27398711 88430 RMVar_ID_88430 Human_SNP_ID_10305000 m1A Human chr1 - 39576084 39576084 39576084 GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCCAGCTCGTCCTCGCCGCGCCGGTGCCACCTGTGA GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCCTGCTCGTCCTCGCCGCGCCGGTGCCACCTGTGA T A PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39575991..39576092 32194978 MeRIP-seq:(Medium) rs1184138627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24260,Human_RBP_ID_354974,Human_RBP_ID_4095795,Human_RBP_ID_8753921,Human_RBP_ID_9319943,Human_RBP_ID_9358702,Human_RBP_ID_18574693,Human_RBP_ID_22023246,Human_RBP_ID_22488139,Human_RBP_ID_26798219,Human_RBP_ID_26864553,Human_RBP_ID_27398711 88431 RMVar_ID_88431 Human_SNP_ID_10305001 m1A Human chr1 - 39576084 39576084 39576084 GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCCAGCTCGTCCTCGCCGCGCCGGTGCCACCTGTGA GTTTCCGTCCCGTCTCCAAGCCCGCCGACTCCCGCTCGTCCTCGCCGCGCCGGTGCCACCTGTGA T G PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39575991..39576092 32194978 MeRIP-seq:(Medium) rs1184138627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24260,Human_RBP_ID_354974,Human_RBP_ID_4095795,Human_RBP_ID_8753921,Human_RBP_ID_9319943,Human_RBP_ID_9358702,Human_RBP_ID_18574693,Human_RBP_ID_22023246,Human_RBP_ID_22488139,Human_RBP_ID_26798219,Human_RBP_ID_26864553,Human_RBP_ID_27398711 88432 RMVar_ID_88432 Human_SNP_ID_10305231 m1A Human chr1 - 39576676 39576673 39576676 ATCTGAAAACGCTTCAAAATCCTGAAAAAAAAAAAGGAAAAGAAAAAACGAATCCTCGGAGAACC ATCTGAAAACGCTTCAAAATCCTGAAAAAAAA___GGAAAAGAAAAAACGAATCCTCGGAGAACC CTTT C PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39576626..39576675 32194978 MeRIP-seq:(Medium) rs906922777 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_24263,Human_RBP_ID_1747770 88433 RMVar_ID_88433 Human_SNP_ID_10305232 m1A Human chr1 - 39576676 39576673 39576676 ATCTGAAAACGCTTCAAAATCCTGAAAAAAAAAAAGGAAAAGAAAAAACGAATCCTCGGAGAACC ATCTGAAAACGCTTCAAAATCCTGAAAAAAAA__AGGAAAAGAAAAAACGAATCCTCGGAGAACC CTTT CT PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39576626..39576675 32194978 MeRIP-seq:(Medium) rs906922777 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24263,Human_RBP_ID_1747770 88434 RMVar_ID_88434 Human_SNP_ID_10305233 m1A Human chr1 - 39576676 39576673 39576676 ATCTGAAAACGCTTCAAAATCCTGAAAAAAAAAAAGGAAAAGAAAAAACGAATCCTCGGAGAACC ATCTGAAAACGCTTCAAAATCCTGAAAAAAAA_AAGGAAAAGAAAAAACGAATCCTCGGAGAACC CTTT CTT PABPC4 Ensembl:ENSG00000090621 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39576626..39576675 32194978 MeRIP-seq:(Medium) rs906922777 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24263,Human_RBP_ID_1747770 88435 RMVar_ID_88435 Human_SNP_ID_10357314 m1A Human chr1 - 39788730 39788730 39788730 GACAGACGGATTGGCCGAGAGTCCCAGTCCGCAGAGTAGCCCCGGCCTCGAGGCGGTGGCGTCCG GACAGACGGATTGGCCGAGAGTCCCAGTCCGCGGAGTAGCCCCGGCCTCGAGGCGGTGGCGTCCG T C BMP8B Ensembl:ENSG00000116985 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39788682..39788825 26863196 MeRIP-seq:(Medium) rs1411816048 Functional Loss SNV dbSNP153 33..33 33 - - - 88436 RMVar_ID_88436 Human_SNP_ID_10357503 m1A Human chr1 - 39789261 39789261 39789261 CCTGGGGCGCTGCCCAGGCTCACGCGGGAGCCAGGTGGGGGCGCGGGGAGGAGCAGCTGAGCAGG CCTGGGGCGCTGCCCAGGCTCACGCGGGAGCCCGGTGGGGGCGCGGGGAGGAGCAGCTGAGCAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:39789006..39789325 26863196 MeRIP-seq:(Medium) rs1012986322 Functional Loss SNV dbSNP153 33..33 33 - - - 88437 RMVar_ID_88437 Human_SNP_ID_10381061 m1A Human chr1 - 39883182 39883182 39883182 AGGGGGTAGGTAAAGGGAGCCCATACTTACTAAGCACCCGCCGCATGCCAGACACAGTGCCAGAT AGGGGGTAGGTAAAGGGAGCCCATACTTACTACGCACCCGCCGCATGCCAGACACAGTGCCAGAT T G TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:39883173..39883276 26863196 MeRIP-seq:(Medium) rs549148043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10982141,Human_RBP_ID_18574780 88438 RMVar_ID_88438 Human_SNP_ID_10381170 m1A Human chr1 - 39883443 39883441 39883443 CTGCACGAGCAGTTCCCGTGGGCAGTGGGCTCAGGGGCCTGCAACGGACCCTACCTCTTGTAGTG CTGCACGAGCAGTTCCCGTGGGCAGTGGGCTC__GGGCCTGCAACGGACCCTACCTCTTGTAGTG CCT C TRIT1 Ensembl:ENSG00000043514 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39883378..39883446 26863196 MeRIP-seq:(Medium) rs1408101254 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_355084,Human_RBP_ID_4073919,Human_RBP_ID_9271366,Human_RBP_ID_18415513,Human_RBP_ID_22430478,Human_RBP_ID_22488155 88439 RMVar_ID_88439 Human_SNP_ID_10385513 m1A Human chr1 + 39901827 39901827 39901827 CCCGCAGCCTCACCTCGCTCCAGCCGCCCGCCACCTGGAGCGGACCGGCTCCCCGCCGGCTCGGG CCCGCAGCCTCACCTCGCTCCAGCCGCCCGCCGCCTGGAGCGGACCGGCTCCCCGCCGGCTCGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39901781..39901902 26863196 MeRIP-seq:(Medium) rs1362725538 Functional Loss SNV dbSNP153 33..33 33 - - - 88440 RMVar_ID_88440 Human_SNP_ID_10400572 m1A Human chr1 - 39961348 39961347 39961348 CGAGACTCTGTCTCAAACAAACAAACAAAAAAAGCGGGGGGGGGGGGGGGGGGGCGGGGGCGGGA CGAGACTCTGTCTCAAACAAACAAACAAAAAA_GCGGGGGGGGGGGGGGGGGGGCGGGGGCGGGA CT C HSALNG0002827 RNACentral:URS0000EB5EC5 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:39961318..39961448 26863196 MeRIP-seq:(Medium) rs1371896357 Functional Loss DEL dbSNP153 33..33 33 - - - 88441 RMVar_ID_88441 Human_SNP_ID_10420550 m1A Human chr1 + 40040793 40040793 40040793 GAGCGGCTGATCGCAGTCCGGAGGTGAGGCGGAACTCTGAGGTGAGGGTGTGCAGCTTGGTAGGG GAGCGGCTGATCGCAGTCCGGAGGTGAGGCGGCACTCTGAGGTGAGGGTGTGCAGCTTGGTAGGG A C CAP1 Ensembl:ENSG00000131236 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:40040696..40040921 26863196 MeRIP-seq:(Medium) rs1455092121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742639,Human_RBP_ID_803550,Human_RBP_ID_4073920,Human_RBP_ID_19034631,Human_RBP_ID_23255518 Human_Splice_Rec_52713,Human_Splice_Rec_52721,Human_Splice_Rec_52745,Human_Splice_Rec_52773,Human_Splice_Rec_52797,Human_Splice_Rec_52821,Human_Splice_Rec_52875,Human_Splice_Rec_52889 RMVar_hsa_circ_116220,RMVar_hsa_circ_131994,RMVar_hsa_circ_131993,RMVar_hsa_circ_378856 88442 RMVar_ID_88442 Human_SNP_ID_10427493 m1A Human chr1 - 40069759 40069759 40069759 TAGGTGCAGAGAATGGTTTGGGGCCACTGCGTACTGGACCACTCTGAGCCTTCAGGGCAGGGTTC TAGGTGCAGAGAATGGTTTGGGGCCACTGCGTGCTGGACCACTCTGAGCCTTCAGGGCAGGGTTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:40069751..40069850 26863196 MeRIP-seq:(Medium) rs11556939 Functional Loss SNV dbSNP153 33..33 33 - - - 88443 RMVar_ID_88443 Human_SNP_ID_10427498 m1A Human chr1 - 40069766 40069766 40069766 TGGGGTTTAGGTGCAGAGAATGGTTTGGGGCCACTGCGTACTGGACCACTCTGAGCCTTCAGGGC TGGGGTTTAGGTGCAGAGAATGGTTTGGGGCCTCTGCGTACTGGACCACTCTGAGCCTTCAGGGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:40069715..40069875 26863196 MeRIP-seq:(Medium) rs1026261572 Functional Loss SNV dbSNP153 33..33 33 - - - 88444 RMVar_ID_88444 Human_SNP_ID_10427505 m1A Human chr1 + 40069803 40069788 40069804 CCAAACCATTCTCTGCACCTAAACCCCAAACCAGCCCATCCCCCAAACGAGCCACAAAGAAGGAG CCAAACCATTCTCTGCAC________________CCCATCCCCCAAACGAGCCACAAAGAAGGAG CCTAAACCCCAAACCAG C CAP1 Ensembl:ENSG00000131236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40069755..40069825 26863196 MeRIP-seq:(Medium) rs761794847 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_742644,Human_RBP_ID_3933336,Human_RBP_ID_17751014,Human_RBP_ID_22427158,Human_RBP_ID_27398744 Human_Splice_Rec_52659,Human_Splice_Rec_52683,Human_Splice_Rec_52737,Human_Splice_Rec_52789,Human_Splice_Rec_52813,Human_Splice_Rec_52837,Human_Splice_Rec_52911,Human_Splice_Rec_52919 Human_miRNA_ID_2652804,Human_miRNA_ID_2753997 RMVar_hsa_circ_116220,RMVar_hsa_circ_131993,RMVar_hsa_circ_2969,RMVar_hsa_circ_82840,RMVar_hsa_circ_90394,RMVar_hsa_circ_131997,RMVar_hsa_circ_87195,RMVar_hsa_circ_131999,RMVar_hsa_circ_113991,RMVar_hsa_circ_132000,RMVar_hsa_circ_91905,RMVar_hsa_circ_118722,RMVar_hsa_circ_132001,RMVar_hsa_circ_105035,RMVar_hsa_circ_132002,RMVar_hsa_circ_132004,RMVar_hsa_circ_53600,RMVar_hsa_circ_132003 88445 RMVar_ID_88445 Human_SNP_ID_10427513 m1A Human chr1 + 40069803 40069800 40069804 CCAAACCATTCTCTGCACCTAAACCCCAAACCAGCCCATCCCCCAAACGAGCCACAAAGAAGGAG CCAAACCATTCTCTGCACCTAAACCCCAAA____CCCATCCCCCAAACGAGCCACAAAGAAGGAG ACCAG A CAP1 Ensembl:ENSG00000131236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40069755..40069825 26863196 MeRIP-seq:(Medium) rs762977570 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_742644,Human_RBP_ID_3933336,Human_RBP_ID_17751014,Human_RBP_ID_22427158,Human_RBP_ID_27398744 Human_Splice_Rec_52659,Human_Splice_Rec_52683,Human_Splice_Rec_52737,Human_Splice_Rec_52789,Human_Splice_Rec_52813,Human_Splice_Rec_52837,Human_Splice_Rec_52911,Human_Splice_Rec_52919 Human_miRNA_ID_2652804,Human_miRNA_ID_2753997 RMVar_hsa_circ_116220,RMVar_hsa_circ_131993,RMVar_hsa_circ_2969,RMVar_hsa_circ_82840,RMVar_hsa_circ_90394,RMVar_hsa_circ_131997,RMVar_hsa_circ_87195,RMVar_hsa_circ_131999,RMVar_hsa_circ_113991,RMVar_hsa_circ_132000,RMVar_hsa_circ_91905,RMVar_hsa_circ_118722,RMVar_hsa_circ_132001,RMVar_hsa_circ_105035,RMVar_hsa_circ_132002,RMVar_hsa_circ_132004,RMVar_hsa_circ_53600,RMVar_hsa_circ_132003 88446 RMVar_ID_88446 Human_SNP_ID_10427515 m1A Human chr1 + 40069803 40069801 40069804 CCAAACCATTCTCTGCACCTAAACCCCAAACCAGCCCATCCCCCAAACGAGCCACAAAGAAGGAG CCAAACCATTCTCTGCACCTAAACCCCAAAC___CCCATCCCCCAAACGAGCCACAAAGAAGGAG CCAG C CAP1 Ensembl:ENSG00000131236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40069755..40069825 26863196 MeRIP-seq:(Medium) rs751754089 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_742644,Human_RBP_ID_3933336,Human_RBP_ID_17751014,Human_RBP_ID_22427158,Human_RBP_ID_27398744 Human_Splice_Rec_52659,Human_Splice_Rec_52683,Human_Splice_Rec_52737,Human_Splice_Rec_52789,Human_Splice_Rec_52813,Human_Splice_Rec_52837,Human_Splice_Rec_52911,Human_Splice_Rec_52919 Human_miRNA_ID_2652804,Human_miRNA_ID_2753997 RMVar_hsa_circ_116220,RMVar_hsa_circ_131993,RMVar_hsa_circ_2969,RMVar_hsa_circ_82840,RMVar_hsa_circ_90394,RMVar_hsa_circ_131997,RMVar_hsa_circ_87195,RMVar_hsa_circ_131999,RMVar_hsa_circ_113991,RMVar_hsa_circ_132000,RMVar_hsa_circ_91905,RMVar_hsa_circ_118722,RMVar_hsa_circ_132001,RMVar_hsa_circ_105035,RMVar_hsa_circ_132002,RMVar_hsa_circ_132004,RMVar_hsa_circ_53600,RMVar_hsa_circ_132003 88447 RMVar_ID_88447 Human_SNP_ID_10428199 m1A Human chr1 + 40072267 40072267 40072267 AGAGATGACTTTAAAAGGAAAAAAAAAAAAAAAAAAACCCACATGATTTCAAGGAGTCTGGCATT AGAGATGACTTTAAAAGGAAAAAAAAAAAAAACAAAACCCACATGATTTCAAGGAGTCTGGCATT A C CAP1 Ensembl:ENSG00000131236 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1460714494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19709 Human_miRNA_ID_2296677 RMVar_hsa_circ_116220,RMVar_hsa_circ_131993,RMVar_hsa_circ_131997,RMVar_hsa_circ_87195,RMVar_hsa_circ_113991,RMVar_hsa_circ_132000,RMVar_hsa_circ_91905,RMVar_hsa_circ_118722,RMVar_hsa_circ_132002,RMVar_hsa_circ_132004 88448 RMVar_ID_88448 Human_SNP_ID_10428539 m1A Human chr1 + 40073553 40073551 40073554 TGATGATAAGATGATAGCACAGAGGGCAACGTACTGAGAGAGGAAGGCAGCCTTAAGAAATGATG TGATGATAAGATGATAGCACAGAGGGCAACG___TGAGAGAGGAAGGCAGCCTTAAGAAATGATG GTAC G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:40073505..40073606 32194978 MeRIP-seq:(Medium) rs375843850 Functional Loss DEL dbSNP153 32..34 33 - - - 88449 RMVar_ID_88449 Human_SNP_ID_10428541 m1A Human chr1 + 40073553 40073553 40073553 TGATGATAAGATGATAGCACAGAGGGCAACGTACTGAGAGAGGAAGGCAGCCTTAAGAAATGATG TGATGATAAGATGATAGCACAGAGGGCAACGTGCTGAGAGAGGAAGGCAGCCTTAAGAAATGATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:40073505..40073606 32194978 MeRIP-seq:(Medium) rs1229573645 Functional Loss SNV dbSNP153 33..33 33 - - - 88450 RMVar_ID_88450 Human_SNP_ID_10433092 m1A Human chr1 + 40091369 40091369 40091369 TGTCCCCCAACCGAGATCAGATTGATCATGGGAGGTGAAGGGCATCTCTGAGCCACTGCCCTCCT TGTCCCCCAACCGAGATCAGATTGATCATGGGGGGTGAAGGGCATCTCTGAGCCACTGCCCTCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:40089575..40092067 32194978 MeRIP-seq:(Medium) rs1222439879 Functional Loss SNV dbSNP153 33..33 33 - - - 88451 RMVar_ID_88451 Human_SNP_ID_10433457 m1A Human chr1 - 40092509 40092509 40092509 TCATGAGTTTCCATCATTGTGTTTTGTTGGCTAGGAGACAGCTGTTGCAATCCCTTAAGCATGGG TCATGAGTTTCCATCATTGTGTTTTGTTGGCTGGGAGACAGCTGTTGCAATCCCTTAAGCATGGG T C PPT1 Ensembl:ENSG00000131238 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:40092451..40092569 26863410 MeRIP-seq:(Medium) rs386833630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2146917,Human_RBP_ID_3312839,Human_RBP_ID_4052362,Human_RBP_ID_22429280 88452 RMVar_ID_88452 Human_SNP_ID_10434598 m1A Human chr1 - 40097156 40097156 40097156 GACCTGCGCTTCTCGGGCGCTGCAGCATCTGGACCCGCCGGCGCCGCTGCCGTTGGTGATCTGGC GACCTGCGCTTCTCGGGCGCTGCAGCATCTGGGCCCGCCGGCGCCGCTGCCGTTGGTGATCTGGC T C PPT1 Ensembl:ENSG00000131238 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:40097101..40097250 26863410 MeRIP-seq:(Medium) rs749909390 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_223891,Human_RBP_ID_355182,Human_RBP_ID_4072739,Human_RBP_ID_5311658,Human_RBP_ID_5434119,Human_RBP_ID_9319951,Human_RBP_ID_22428293,Human_RBP_ID_22750900,Human_RBP_ID_23394150,Human_RBP_ID_26864602,Human_RBP_ID_27398759 Human_Splice_Rec_52929,Human_Splice_Rec_52945,Human_Splice_Rec_52971,Human_Splice_Rec_52987,Human_Splice_Rec_53003,Human_Splice_Rec_53019,Human_Splice_Rec_53037,Human_Splice_Rec_53051,Human_Splice_Rec_53065,Human_Splice_Rec_53081,Human_Splice_Rec_53091,Human_Splice_Rec_53121,Human_Splice_Rec_53129,Human_Splice_Rec_53141,Human_Splice_Rec_53159 88453 RMVar_ID_88453 Human_SNP_ID_10434599 m1A Human chr1 - 40097156 40097156 40097156 GACCTGCGCTTCTCGGGCGCTGCAGCATCTGGACCCGCCGGCGCCGCTGCCGTTGGTGATCTGGC GACCTGCGCTTCTCGGGCGCTGCAGCATCTGGCCCCGCCGGCGCCGCTGCCGTTGGTGATCTGGC T G PPT1 Ensembl:ENSG00000131238 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:40097101..40097250 26863410 MeRIP-seq:(Medium) rs749909390 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_223891,Human_RBP_ID_355182,Human_RBP_ID_4072739,Human_RBP_ID_5311658,Human_RBP_ID_5434119,Human_RBP_ID_9319951,Human_RBP_ID_22428293,Human_RBP_ID_22750900,Human_RBP_ID_23394150,Human_RBP_ID_26864602,Human_RBP_ID_27398759 Human_Splice_Rec_52929,Human_Splice_Rec_52945,Human_Splice_Rec_52971,Human_Splice_Rec_52987,Human_Splice_Rec_53003,Human_Splice_Rec_53019,Human_Splice_Rec_53037,Human_Splice_Rec_53051,Human_Splice_Rec_53065,Human_Splice_Rec_53081,Human_Splice_Rec_53091,Human_Splice_Rec_53121,Human_Splice_Rec_53129,Human_Splice_Rec_53141,Human_Splice_Rec_53159 88454 RMVar_ID_88454 Human_SNP_ID_10434627 m1A Human chr1 + 40097198 40097198 40097198 GCAGCGCCCGAGAAGCGCAGGTCCATGGCAGGAGAGCCACAGCCAAGAGCCACAGGCAGCCGGGC GCAGCGCCCGAGAAGCGCAGGTCCATGGCAGGTGAGCCACAGCCAAGAGCCACAGGCAGCCGGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:40097067..40097250;chr1:40097075..40097250;chr1:40097058..40097250;chr1:40097074..40097250 26863196 MeRIP-seq:(Medium) rs1322447258 Functional Loss SNV dbSNP153 33..33 33 - - - 88455 RMVar_ID_88455 Human_SNP_ID_10449873 m1A Human chr1 - 40161429 40161429 40161429 ACCGCCGGAGCCTCAGCCCCAGCCCCGGCGACAGCGGCGGCGTCTCCCTTTCCGTCCGCCATCTT ACCGCCGGAGCCTCAGCCCCAGCCCCGGCGACGGCGGCGGCGTCTCCCTTTCCGTCCGCCATCTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:40161376..40161623 26863196 MeRIP-seq:(Medium) rs769946910 Functional Loss SNV dbSNP153 33..33 33 - - - 88456 RMVar_ID_88456 Human_SNP_ID_10474557 m1A Human chr1 - 40257736 40257736 40257736 GGGGCCGGAACTGACTGAGTGGGCCGCAACTGACTGAGTGGGCCGCGGCTCCCGCCTGAGGAGGC GGGGCCGGAACTGACTGAGTGGGCCGCAACTGTCTGAGTGGGCCGCGGCTCCCGCCTGAGGAGGC T A AL050341.2 Ensembl:ENSG00000259943 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:40257690..40257893 26863196 MeRIP-seq:(Medium) rs972511793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073923,Human_RBP_ID_23394274 Human_miRNA_ID_3164053 88457 RMVar_ID_88457 Human_SNP_ID_10483377 m1A Human chr1 + 40293559 40293559 40293559 AGACGAATTAAAAATAACATTTTTTAAGCGACATAAGGATGAAATACTGATGAATCTCTGTGACA AGACGAATTAAAAATAACATTTTTTAAGCGACGTAAGGATGAAATACTGATGAATCTCTGTGACA A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10489432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17453141,Human_RBP_ID_18230500,Human_RBP_ID_22376815 Human_miRNA_ID_1505109 Clinvar_Rec_498 RMVar_hsa_circ_119238,RMVar_hsa_circ_121001,RMVar_hsa_circ_132028,RMVar_hsa_circ_84550,RMVar_hsa_circ_132033,RMVar_hsa_circ_126918,RMVar_hsa_circ_132035,RMVar_hsa_circ_132036 88458 RMVar_ID_88458 Human_SNP_ID_10485251 m1A Human chr1 - 40300979 40300979 40300979 AGAGCACTGATGGGTGAAAAAGTGAGGCCAACACACAGGGCAAGTGGTGTCGATGGAGTCGAAGC AGAGCACTGATGGGTGAAAAAGTGAGGCCAACGCACAGGGCAAGTGGTGTCGATGGAGTCGAAGC T C COL9A2 Ensembl:ENSG00000049089 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40300599..40301046 26863196 MeRIP-seq:(Medium) rs1338018372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18157765 88459 RMVar_ID_88459 Human_SNP_ID_10486429 m1A Human chr1 - 40304091 40304091 40304091 CCCCTCACTGCCCGCTTTCTCCAGGGCTCCCCAGGGAAGACCGGGCCCCGCGGCAAAGTGGTGAG CCCCTCACTGCCCGCTTTCTCCAGGGCTCCCCCGGGAAGACCGGGCCCCGCGGCAAAGTGGTGAG T G COL9A2 Ensembl:ENSG00000049089 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40302783..40305007 26863196 MeRIP-seq:(Medium) rs1301283271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801396,Human_RBP_ID_851462,Human_RBP_ID_5337646,Human_RBP_ID_9358711,Human_RBP_ID_18158298,Human_RBP_ID_18965295,Human_RBP_ID_22750916 Human_Splice_Rec_53262,Human_Splice_Rec_53263,Human_Splice_Rec_53322,Human_Splice_Rec_53323,Human_Splice_Rec_53344,Human_Splice_Rec_53345,Human_Splice_Rec_53360,Human_Splice_Rec_53361 88460 RMVar_ID_88460 Human_SNP_ID_10564094 m1A Human chr1 - 40625455 40625455 40625455 TGTTGAGGATCCCATCTGACATTTGGGGATTCACTGCATGAAGTTGTTCATTTGGGGCTCCAGTT TGTTGAGGATCCCATCTGACATTTGGGGATTCTCTGCATGAAGTTGTTCATTTGGGGCTCCAGTT T A RIMS3 Ensembl:ENSG00000117016 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs570671 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11158,GWAS_ID_11159 RMVar_hsa_circ_103480,RMVar_hsa_circ_265425,RMVar_hsa_circ_132051,RMVar_hsa_circ_91202,RMVar_hsa_circ_132050 88461 RMVar_ID_88461 Human_SNP_ID_10564095 m1A Human chr1 - 40625455 40625455 40625455 TGTTGAGGATCCCATCTGACATTTGGGGATTCACTGCATGAAGTTGTTCATTTGGGGCTCCAGTT TGTTGAGGATCCCATCTGACATTTGGGGATTCGCTGCATGAAGTTGTTCATTTGGGGCTCCAGTT T C RIMS3 Ensembl:ENSG00000117016 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs570671 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11158,GWAS_ID_11159 RMVar_hsa_circ_103480,RMVar_hsa_circ_265425,RMVar_hsa_circ_132051,RMVar_hsa_circ_91202,RMVar_hsa_circ_132050 88462 RMVar_ID_88462 Human_SNP_ID_10564096 m1A Human chr1 - 40625455 40625455 40625455 TGTTGAGGATCCCATCTGACATTTGGGGATTCACTGCATGAAGTTGTTCATTTGGGGCTCCAGTT TGTTGAGGATCCCATCTGACATTTGGGGATTCCCTGCATGAAGTTGTTCATTTGGGGCTCCAGTT T G RIMS3 Ensembl:ENSG00000117016 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs570671 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11158,GWAS_ID_11159 RMVar_hsa_circ_103480,RMVar_hsa_circ_265425,RMVar_hsa_circ_132051,RMVar_hsa_circ_91202,RMVar_hsa_circ_132050 88463 RMVar_ID_88463 Human_SNP_ID_10579815 m1A Human chr1 - 40691729 40691729 40691729 GGAGAACGGAGCGCGCGCGAAGCGGGGGCACAAGCAAGATGGCGGCCACGCCGTTTGCACCGTTT GGAGAACGGAGCGCGCGCGAAGCGGGGGCACACGCAAGATGGCGGCCACGCCGTTTGCACCGTTT T G NFYC-AS1 Ensembl:ENSG00000272145 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:40691668..40691875 26863196 MeRIP-seq:(Medium) rs1160788565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5542991 88464 RMVar_ID_88464 Human_SNP_ID_10579848 m1A Human chr1 - 40691780 40691780 40691780 GGCAATGCAGAGGCCCAGGCGCGGCGGAGGGGAGGGGGAAGTGTGCGTCACGGAGAACGGAGCGC GGCAATGCAGAGGCCCAGGCGCGGCGGAGGGGGGGGGGAAGTGTGCGTCACGGAGAACGGAGCGC T C NFYC-AS1 Ensembl:ENSG00000272145 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40691730..40692069 26863196 MeRIP-seq:(Medium) rs1035624543 Functional Loss SNV dbSNP153 33..33 33 - - - 88465 RMVar_ID_88465 Human_SNP_ID_10579849 m1A Human chr1 - 40691780 40691780 40691780 GGCAATGCAGAGGCCCAGGCGCGGCGGAGGGGAGGGGGAAGTGTGCGTCACGGAGAACGGAGCGC GGCAATGCAGAGGCCCAGGCGCGGCGGAGGGGCGGGGGAAGTGTGCGTCACGGAGAACGGAGCGC T G NFYC-AS1 Ensembl:ENSG00000272145 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40691730..40692069 26863196 MeRIP-seq:(Medium) rs1035624543 Functional Loss SNV dbSNP153 33..33 33 - - - 88466 RMVar_ID_88466 Human_SNP_ID_10621340 m1A Human chr1 + 40861296 40861296 40861296 TTGGGGGAAGAGGGCGGCGAGGGGGAGAGGACACGATCCAAGAACCAGAGTCCGAAAGCTGAAGC TTGGGGGAAGAGGGCGGCGAGGGGGAGAGGACCCGATCCAAGAACCAGAGTCCGAAAGCTGAAGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:40861231..40861418 26863196 MeRIP-seq:(Medium) rs1558052462 Functional Loss SNV dbSNP153 33..33 33 - - - 88467 RMVar_ID_88467 Human_SNP_ID_10621361 m1A Human chr1 + 40861382 40861382 40861382 ACGGCCGAGGCTGGGGTCAGAGAAGTGAAGCCAAACTGTCCTCCCGCAGGAGGCAAGGCCTGGAG ACGGCCGAGGCTGGGGTCAGAGAAGTGAAGCCGAACTGTCCTCCCGCAGGAGGCAAGGCCTGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:40861147..40861441 32194978 MeRIP-seq:(Medium) rs1180836460 Functional Loss SNV dbSNP153 33..33 33 - - - 88468 RMVar_ID_88468 Human_SNP_ID_10621362 m1A Human chr1 + 40861382 40861382 40861382 ACGGCCGAGGCTGGGGTCAGAGAAGTGAAGCCAAACTGTCCTCCCGCAGGAGGCAAGGCCTGGAG ACGGCCGAGGCTGGGGTCAGAGAAGTGAAGCCTAACTGTCCTCCCGCAGGAGGCAAGGCCTGGAG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:40861147..40861441 32194978 MeRIP-seq:(Medium) rs1180836460 Functional Loss SNV dbSNP153 33..33 33 - - - 88469 RMVar_ID_88469 Human_SNP_ID_10621394 m1A Human chr1 - 40861466 40861466 40861466 CTGGGCCCCGCGCGCGCCCTCCGCGAGGGTGGAGGCGGCGGCTGTGTGCGCAGGGCCCGGCACCG CTGGGCCCCGCGCGCGCCCTCCGCGAGGGTGGCGGCGGCGGCTGTGTGCGCAGGGCCCGGCACCG T G CITED4 Ensembl:ENSG00000179862 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:40861410..40861575 26863196 MeRIP-seq:(Medium) rs1233730041 Functional Loss SNV dbSNP153 33..33 33 - - - 88470 RMVar_ID_88470 Human_SNP_ID_10621579 m1A Human chr1 + 40861853 40861853 40861853 GCGCGGCCGCGCGGCCGGGGTACGGCGTCGCCACAGGCTGCAGGTGCGCGATGCCCGCGGCCGGC GCGCGGCCGCGCGGCCGGGGTACGGCGTCGCCCCAGGCTGCAGGTGCGCGATGCCCGCGGCCGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40861802..40861989 26863196 MeRIP-seq:(Medium) rs1450250996 Functional Loss SNV dbSNP153 33..33 33 - - - 88471 RMVar_ID_88471 Human_SNP_ID_10621584 m1A Human chr1 - 40861872 40861872 40861872 CCTTTCCGGCCGTGCCTCCGCCGGCCGCGGGCATCGCGCACCTGCAGCCTGTGGCGACGCCGTAC CCTTTCCGGCCGTGCCTCCGCCGGCCGCGGGCGTCGCGCACCTGCAGCCTGTGGCGACGCCGTAC T C CITED4 Ensembl:ENSG00000179862 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:40861651..40861925 26863196 MeRIP-seq:(Medium) rs960157809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27398875 88472 RMVar_ID_88472 Human_SNP_ID_10621683 m1A Human chr1 - 40862057 40862057 40862057 GGTGCAGAGGCCGCCGTCCGCCGCGGCCGCCCATGGCCCTCATGCGCTCCGGACTCTGCCGCCGT GGTGCAGAGGCCGCCGTCCGCCGCGGCCGCCCGTGGCCCTCATGCGCTCCGGACTCTGCCGCCGT T C CITED4 Ensembl:ENSG00000179862 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:40861726..40862350 26863196 MeRIP-seq:(Medium) rs1191169569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27398878 88473 RMVar_ID_88473 Human_SNP_ID_10625964 m1A Human chr1 + 40879085 40879084 40879086 AGGAAAGAAGGAAGGAAGGAAGGAAGGAAGAAAGAAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA AGGAAAGAAGGAAGGAAGGAAGGAAGGAAGAA__AAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA AAG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40879035..40879119 26863196 MeRIP-seq:(Medium) rs1450202118 Functional Loss DEL dbSNP153 33..34 33 - - - 88474 RMVar_ID_88474 Human_SNP_ID_10625965 m1A Human chr1 + 40879085 40879085 40879085 AGGAAAGAAGGAAGGAAGGAAGGAAGGAAGAAAGAAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA AGGAAAGAAGGAAGGAAGGAAGGAAGGAAGAAGGAAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40879035..40879119 26863196 MeRIP-seq:(Medium) rs1188408956 Functional Loss SNV dbSNP153 33..33 33 - - - 88475 RMVar_ID_88475 Human_SNP_ID_10651510 m1A Human chr1 - 40978946 40978943 40978946 GGAAGCCCGCCCTGAAAAAGTAACTTTGAAGCAGAGACCTAAGTAGACGGCAAAGATGGGAAAGG GGAAGCCCGCCCTGAAAAAGTAACTTTGAAGC___GACCTAAGTAGACGGCAAAGATGGGAAAGG CTCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:40978864..40979009 26863196 MeRIP-seq:(Medium) rs1267944519 Functional Loss DEL dbSNP153 33..35 33 - - - 88476 RMVar_ID_88476 Human_SNP_ID_10651511 m1A Human chr1 - 40978946 40978946 40978946 GGAAGCCCGCCCTGAAAAAGTAACTTTGAAGCAGAGACCTAAGTAGACGGCAAAGATGGGAAAGG GGAAGCCCGCCCTGAAAAAGTAACTTTGAAGCGGAGACCTAAGTAGACGGCAAAGATGGGAAAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:40978864..40979009 26863196 MeRIP-seq:(Medium) rs1423316390 Functional Loss SNV dbSNP153 33..33 33 - - - 88477 RMVar_ID_88477 Human_SNP_ID_10651788 m1A Human chr1 - 40979752 40979752 40979752 GCGACGCGCGCGGAGCCCCGGACAGCCAGTGAACAACCCCGACCGCATGCGCCCGGCAGTCTTTC GCGACGCGCGCGGAGCCCCGGACAGCCAGTGAGCAACCCCGACCGCATGCGCCCGGCAGTCTTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40979701..40979870 26863196 MeRIP-seq:(Medium) rs1243218672 Functional Loss SNV dbSNP153 33..33 33 - - - 88478 RMVar_ID_88478 Human_SNP_ID_10651955 m1A Human chr1 - 40980101 40980101 40980101 CAGCGCGGCAGCGCAGGCCCCGCAGCCTCTGAAGCCGCCCCGCGCCCCGCTTGGCCCCTCTCCCC CAGCGCGGCAGCGCAGGCCCCGCAGCCTCTGAGGCCGCCCCGCGCCCCGCTTGGCCCCTCTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40980083..40980246 26863196 MeRIP-seq:(Medium) rs1393472829 Functional Loss SNV dbSNP153 33..33 33 - - - 88479 RMVar_ID_88479 Human_SNP_ID_10653584 m1A Human chr1 + 40986134 40986134 40986134 TGCCCACATGGAGGTTACCTGTGGGGGAGGCAAACAACAAACATGAAACAAAACGAGACGTCTGT TGCCCACATGGAGGTTACCTGTGGGGGAGGCAGACAACAAACATGAAACAAAACGAGACGTCTGT A G CTPS1 Ensembl:ENSG00000171793 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:40986129..40986471 26863196 MeRIP-seq:(Medium) rs951259298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6131,RMVar_hsa_circ_84087,RMVar_hsa_circ_116709,RMVar_hsa_circ_125619,RMVar_hsa_circ_132069,RMVar_hsa_circ_132070,RMVar_hsa_circ_132071,RMVar_hsa_circ_357257,RMVar_hsa_circ_377832,RMVar_hsa_circ_12488,RMVar_hsa_circ_101000,RMVar_hsa_circ_132072 88480 RMVar_ID_88480 Human_SNP_ID_10660602 m1A Human chr1 - 41014944 41014944 41014944 TTTGCACTCCTGCCTCGGGGCCTCTGCGCTACATAGCGGCCTATTTCCTTTCCTCTTCACCTTCA TTTGCACTCCTGCCTCGGGGCCTCTGCGCTACGTAGCGGCCTATTTCCTTTCCTCTTCACCTTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41014839..41015140 26863196 MeRIP-seq:(Medium) rs77787343 Functional Loss SNV dbSNP153 33..33 33 - - - 88481 RMVar_ID_88481 Human_SNP_ID_10661618 m1A Human chr1 - 41017966 41017966 41017966 CAGTGCCATTGTGCACCAGCAGATCGTGGGCAAGGACCAGCTCTTCCAGGGTGCCTTCCTGGGCA CAGTGCCATTGTGCACCAGCAGATCGTGGGCACGGACCAGCTCTTCCAGGGTGCCTTCCTGGGCA T G SLFNL1 Ensembl:ENSG00000171790 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:41017938..41018189 32194978 MeRIP-seq:(Medium) rs556560244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_54646 88482 RMVar_ID_88482 Human_SNP_ID_10666322 m1A Human chr1 + 41035572 41035572 41035572 AGGCCTTTCTCTATTCACTGATGGACACACTCAATCTTCCCTCCTCTCTCAGAGAAAGTGTGCCT AGGCCTTTCTCTATTCACTGATGGACACACTCCATCTTCCCTCCTCTCTCAGAGAAAGTGTGCCT A C SLFNL1-AS1 Ensembl:ENSG00000281207 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:41035563..41035680 26863196 MeRIP-seq:(Medium) rs1039322309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17751384,Human_RBP_ID_19358034 88483 RMVar_ID_88483 Human_SNP_ID_10696907 m1A Human chr1 + 41170726 41170726 41170726 TTTCTTTGCTCTCCTTCACAGGAAAATTTAAGAGTTATCTGCAGTTATTGCCTCCTCACTACTTC TTTCTTTGCTCTCCTTCACAGGAAAATTTAAGTGTTATCTGCAGTTATTGCCTCCTCACTACTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41170724..41170913 26863196 MeRIP-seq:(Medium) rs1487183262 Functional Loss SNV dbSNP153 33..33 33 - - - 88484 RMVar_ID_88484 Human_SNP_ID_10707331 m1A Human chr1 - 41215533 41215533 41215533 CAGATAAGAGGAGGGACTGCAAATCATTTGGAATAACTTAGGGAAAGAAGGTAAAGAGAAGATTG CAGATAAGAGGAGGGACTGCAAATCATTTGGAGTAACTTAGGGAAAGAAGGTAAAGAGAAGATTG T C SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41215531..41215657 26863196 MeRIP-seq:(Medium) rs564500117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18575203 RMVar_hsa_circ_83050,RMVar_hsa_circ_132108 88485 RMVar_ID_88485 Human_SNP_ID_10712442 m1A Human chr1 - 41238669 41238669 41238669 AGCAGAGGCGAAGGTCAGTAAAGCTGAGTATGACAAGGAATTTGGAGGCTAGTGTATTGAATGAG AGCAGAGGCGAAGGTCAGTAAAGCTGAGTATGTCAAGGAATTTGGAGGCTAGTGTATTGAATGAG T A SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41238466..41238781 26863196 MeRIP-seq:(Medium) rs1041831836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9521456 RMVar_hsa_circ_83050,RMVar_hsa_circ_132108 88486 RMVar_ID_88486 Human_SNP_ID_10712443 m1A Human chr1 + 41238671 41238671 41238671 CATTCAATACACTAGCCTCCAAATTCCTTGTCATACTCAGCTTTACTGACCTTCGCCTCTGCTGT CATTCAATACACTAGCCTCCAAATTCCTTGTCGTACTCAGCTTTACTGACCTTCGCCTCTGCTGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41238442..41238810 26863196 MeRIP-seq:(Medium) rs1391250657 Functional Loss SNV dbSNP153 33..33 33 - - - 88487 RMVar_ID_88487 Human_SNP_ID_10713023 m1A Human chr1 - 41241233 41241232 41241233 CTCCTGACTGGAAGAGAATTTAAAAGTCATCTAGGGGCGCTTTCTCCCATCCCATGCCAAAGTGA CTCCTGACTGGAAGAGAATTTAAAAGTCATCT_GGGGCGCTTTCTCCCATCCCATGCCAAAGTGA CT C SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41241226..41241734 26863196 MeRIP-seq:(Medium) rs1026143721 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_83050,RMVar_hsa_circ_132108 88488 RMVar_ID_88488 Human_SNP_ID_10713024 m1A Human chr1 - 41241233 41241233 41241233 CTCCTGACTGGAAGAGAATTTAAAAGTCATCTAGGGGCGCTTTCTCCCATCCCATGCCAAAGTGA CTCCTGACTGGAAGAGAATTTAAAAGTCATCTGGGGGCGCTTTCTCCCATCCCATGCCAAAGTGA T C SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41241226..41241734 26863196 MeRIP-seq:(Medium) rs1444505598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83050,RMVar_hsa_circ_132108 88489 RMVar_ID_88489 Human_SNP_ID_10713050 m1A Human chr1 + 41241335 41241333 41241335 CGATGCTCTCGGGCTGGCACACAACTGTGCCCACGTGTCTGGCCCCCAGGGCCGCTGTGGCTCAC CGATGCTCTCGGGCTGGCACACAACTGTGCC__CGTGTCTGGCCCCCAGGGCCGCTGTGGCTCAC CCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41241331..41241675 26863196 MeRIP-seq:(Medium) rs1205818191 Functional Loss DEL dbSNP153 32..33 33 - - - 88490 RMVar_ID_88490 Human_SNP_ID_10713080 m1A Human chr1 + 41241439 41241439 41241439 GCACTGGGGCAGGCGGCACACGTGAGTCGGCCAGCCGGGGCCCAGCCCCCAGGACGCTGCTGACA GCACTGGGGCAGGCGGCACACGTGAGTCGGCCGGCCGGGGCCCAGCCCCCAGGACGCTGCTGACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:41241431..41241515 26863196 MeRIP-seq:(Medium) rs12125555 Functional Loss SNV dbSNP153 33..33 33 - - - 88491 RMVar_ID_88491 Human_SNP_ID_10713486 m1A Human chr1 - 41242449 41242448 41242450 CTCGTCCCCGCCCTCGCGCCCTCTCAGGCCTCAGTTTTCCCATCTACAGGACGCAGACCGGAGAG CTCGTCCCCGCCCTCGCGCCCTCTCAGGCCT__GTTTTCCCATCTACAGGACGCAGACCGGAGAG CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41242399..41242487 26863196 MeRIP-seq:(Medium) rs1170069909 Functional Loss DEL dbSNP153 32..33 33 - - - 88492 RMVar_ID_88492 Human_SNP_ID_10740893 m1A Human chr1 + 41361505 41361505 41361505 GGCGCTGGAGCCGGAGCGGCGGCGGCGGCAGCATTCACCGGGCGGCGGCGGCGCGGGCTCCGGCA GGCGCTGGAGCCGGAGCGGCGGCGGCGGCAGCTTTCACCGGGCGGCGGCGGCGCGGGCTCCGGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41361471..41361794 26863196 MeRIP-seq:(Medium) rs567631470 Functional Loss SNV dbSNP153 33..33 33 - - - 88493 RMVar_ID_88493 Human_SNP_ID_10741105 m1A Human chr1 + 41362120 41362109 41362121 GCGGGCCGGAGCGCCGGGCTACGGCCCCGGCGATGGCCCCAGCGCCGCCCCTGGGCGCGGAGGTC GCGGGCCGGAGCGCCGGGCTAC____________GGCCCCAGCGCCGCCCCTGGGCGCGGAGGTC CGGCCCCGGCGAT C FOXO6 Ensembl:ENSG00000204060 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:41362070..41362213 26863196 MeRIP-seq:(Medium) rs752209952 Functional Loss DEL dbSNP153 23..34 33 - - - 88494 RMVar_ID_88494 Human_SNP_ID_10741119 m1A Human chr1 - 41362139 41362139 41362139 TCGCTTTCCGCAGCGGTCCGACCTCCGCGCCCAGGGGCGGCGCTGGGGCCATCGCCGGGGCCGTA TCGCTTTCCGCAGCGGTCCGACCTCCGCGCCCTGGGGCGGCGCTGGGGCCATCGCCGGGGCCGTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41362091..41362159 26863196 MeRIP-seq:(Medium) rs1319240903 Functional Loss SNV dbSNP153 33..33 33 - - - 88495 RMVar_ID_88495 Human_SNP_ID_10742320 m1A Human chr1 - 41366777 41366777 41366777 TTCGAACCCGCAAACCCCCCGCGCCGTTCATTACCTTAACGCGAGTTAAAAATAACCGTCTCATC TTCGAACCCGCAAACCCCCCGCGCCGTTCATTTCCTTAACGCGAGTTAAAAATAACCGTCTCATC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41366669..41366807 26863196 MeRIP-seq:(Medium) rs1270309327 Functional Loss SNV dbSNP153 33..33 33 - - - 88496 RMVar_ID_88496 Human_SNP_ID_10743290 m1A Human chr1 + 41371077 41371076 41371078 AGGTAGAAGAGGGGAAGGGAGACAAAGCAGACAAAGAGGGTCAAGGCCTCAGGACTGTGTGGGGA AGGTAGAAGAGGGGAAGGGAGACAAAGCAGAC__AGAGGGTCAAGGCCTCAGGACTGTGTGGGGA CAA C FOXO6 Ensembl:ENSG00000204060 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41371065..41371173 26863196 MeRIP-seq:(Medium) rs1382912588 Functional Loss DEL dbSNP153 33..34 33 - - - 88497 RMVar_ID_88497 Human_SNP_ID_10745666 m1A Human chr1 - 41381571 41381571 41381571 ACAAGGACGCGGGTGGGAGTCGGGGGGTGAGGAGGCCATGGGGAGAGAGGGGACGTGATGGAAAG ACAAGGACGCGGGTGGGAGTCGGGGGGTGAGGCGGCCATGGGGAGAGAGGGGACGTGATGGAAAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41381503..41381673 26863196 MeRIP-seq:(Medium) rs1413130920 Functional Loss SNV dbSNP153 33..33 33 - - - 88498 RMVar_ID_88498 Human_SNP_ID_10745668 m1A Human chr1 + 41381576 41381576 41381576 CATCACGTCCCCTCTCTCCCCATGGCCTCCTCACCCCCCGACTCCCACCCGCGTCCTTGTCTCTG CATCACGTCCCCTCTCTCCCCATGGCCTCCTCCCCCCCCGACTCCCACCCGCGTCCTTGTCTCTG A C FOXO6 Ensembl:ENSG00000204060 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41381526..41381845 26863196 MeRIP-seq:(Medium) rs1191444367 Functional Loss SNV dbSNP153 33..33 33 - - - 88499 RMVar_ID_88499 Human_SNP_ID_10746290 m1A Human chr1 - 41383162 41383160 41383162 CTGCTCAGGGTGGATGGATATAGGTAGGTGTGAGTTTTCCGCAGAGGGTTGCTGGCTTCGGGTGG CTGCTCAGGGTGGATGGATATAGGTAGGTGTG__TTTTCCGCAGAGGGTTGCTGGCTTCGGGTGG ACT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:41382992..41383517 26863196 MeRIP-seq:(Medium) rs979004519 Functional Loss DEL dbSNP153 33..34 33 - - - 88500 RMVar_ID_88500 Human_SNP_ID_10756538 m1A Human chr1 - 41425219 41425213 41425219 ACCACACATACACACATAACACACATGCACACACACACCACACATATCTATACACCACACCAAAC ACCACACATACACACATAACACACATGCACAC______CACACATATCTATACACCACACCAAAC GGTGTGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41425171..41425254 26863196 MeRIP-seq:(Medium) rs923065102 Functional Loss DEL dbSNP153 33..38 33 - - - 88501 RMVar_ID_88501 Human_SNP_ID_10756539 m1A Human chr1 - 41425219 41425213 41425219 ACCACACATACACACATAACACACATGCACACACACACCACACATATCTATACACCACACCAAAC ACCACACATACACACATAACACACATGCACAC__ACACCACACATATCTATACACCACACCAAAC GGTGTGT GGTGT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41425171..41425254 26863196 MeRIP-seq:(Medium) rs923065102 Functional Loss DEL dbSNP153 33..34 33 - - - 88502 RMVar_ID_88502 Human_SNP_ID_10756918 m1A Human chr1 + 41426259 41426259 41426259 AGGGGCTTGGGCAGGACTGGGTGGTAGTTTGGATGTGAGTTGGGAGGGGCTTGGACAGGACTGGG AGGGGCTTGGGCAGGACTGGGTGGTAGTTTGGGTGTGAGTTGGGAGGGGCTTGGACAGGACTGGG A G HSALNG0002951 RNACentral:URS0000EA257A lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:41425992..41426371 26863196 MeRIP-seq:(Medium) rs1219066317 Functional Loss SNV dbSNP153 33..33 33 - - - 88503 RMVar_ID_88503 Human_SNP_ID_10779314 m1A Human chr1 - 41513180 41513180 41513180 ACAGGCCTCAGCCCCAAGCCCACCTGGCCTGCACGTGGACCCAGGAAGGGGCATGGGCGCTCTCC ACAGGCCTCAGCCCCAAGCCCACCTGGCCTGCTCGTGGACCCAGGAAGGGGCATGGGCGCTCTCC T A HIVEP3 Ensembl:ENSG00000127124 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41513131..41513307 26863196 MeRIP-seq:(Medium) rs999962934 Functional Loss SNV dbSNP153 33..33 33 - - - 88504 RMVar_ID_88504 Human_SNP_ID_10782502 m1A Human chr1 + 41526386 41526384 41526386 ACCCTCACACTCACCCTCACACGCTCGCCCTCACACTCACACATGCCCACACCCCCACACTCACC ACCCTCACACTCACCCTCACACGCTCGCCCT__CACTCACACATGCCCACACCCCCACACTCACC TCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:41526356..41526481 26863196 MeRIP-seq:(Medium) rs1405858610 Functional Loss DEL dbSNP153 32..33 33 - - - 88505 RMVar_ID_88505 Human_SNP_ID_10783185 m1A Human chr1 - 41527259 41527259 41527259 TGTATGTGAGGGTGTGTGAGGGTGAGCATGTGAGGGTGTGTGTGTGTGAGGTGAGTGTGTGAGGG TGTATGTGAGGGTGTGTGAGGGTGAGCATGTGTGGGTGTGTGTGTGTGAGGTGAGTGTGTGAGGG T A HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41527214..41527602 26863196 MeRIP-seq:(Medium) rs1387375068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23395152 RMVar_hsa_circ_15419 88506 RMVar_ID_88506 Human_SNP_ID_10783304 m1A Human chr1 - 41527403 41527378 41527404 TGTGGAGTGTGAGTGAAGGTGAGTGTGAGGGCAGGGTGTGGAGTGTGAGTGCGAGTGTGAGTGCA TGTGGAGTGTGAGTGAAGGTGAGTGTGAGGG__________________________TGAGTGCA ACACTCGCACTCACACTCCACACCCTG A HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:41527277..41527423 26863196 MeRIP-seq:(Medium) rs1199680528 Functional Loss DEL dbSNP153 32..57 33 - - - RMVar_hsa_circ_15419 88507 RMVar_ID_88507 Human_SNP_ID_10783324 m1A Human chr1 - 41527403 41527403 41527403 TGTGGAGTGTGAGTGAAGGTGAGTGTGAGGGCAGGGTGTGGAGTGTGAGTGCGAGTGTGAGTGCA TGTGGAGTGTGAGTGAAGGTGAGTGTGAGGGCGGGGTGTGGAGTGTGAGTGCGAGTGTGAGTGCA T C HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:41527277..41527423 26863196 MeRIP-seq:(Medium) rs1170965275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15419 88508 RMVar_ID_88508 Human_SNP_ID_10783618 m1A Human chr1 - 41527965 41527965 41527965 GTGCGGGAGTGTGGAGTGTGAAGGTGAATGCAAGGGTGTGGGGTGCATGTGTGAGGGTGACCATG GTGCGGGAGTGTGGAGTGTGAAGGTGAATGCACGGGTGTGGGGTGCATGTGTGAGGGTGACCATG T G HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41527921..41528024 26863196 MeRIP-seq:(Medium) rs937411144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15419 88509 RMVar_ID_88509 Human_SNP_ID_10784525 m1A Human chr1 - 41529699 41529697 41529699 CGTGTGTATGTGTAAATATGGGGTATATGAGTATTCAAGTGGAGATGCAAGTGTGGTTGTGGGAG CGTGTGTATGTGTAAATATGGGGTATATGAGT__TCAAGTGGAGATGCAAGTGTGGTTGTGGGAG AAT A HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41529676..41529841 26863196 MeRIP-seq:(Medium) rs1158254696 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_15419 88510 RMVar_ID_88510 Human_SNP_ID_10785689 m1A Human chr1 - 41533395 41533395 41533395 GCTTGGGGCTGGTTGATTTGTGATGGGAAGAGAGCTGGGCTTGTGTCTGTGGTGGTGGAAGGGGC GCTTGGGGCTGGTTGATTTGTGATGGGAAGAGCGCTGGGCTTGTGTCTGTGGTGGTGGAAGGGGC T G HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41533387..41533499 26863196 MeRIP-seq:(Medium) rs753407334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15419 88511 RMVar_ID_88511 Human_SNP_ID_10785751 m1A Human chr1 - 41533621 41533621 41533621 AGGGAATGAGGTGCCTCCAGAAGGCCAGCAAGAGGGCGGACAGGATGAGGCAAATGGACTTTCAA AGGGAATGAGGTGCCTCCAGAAGGCCAGCAAGCGGGCGGACAGGATGAGGCAAATGGACTTTCAA T G HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41533609..41533736 26863196 MeRIP-seq:(Medium) rs770005762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15419 88512 RMVar_ID_88512 Human_SNP_ID_10788183 m1A Human chr1 + 41544659 41544629 41544659 TCGCTACTACCATCACCACCACCACTACCACCACTACTACCACCACCACCACCTCTACCACCACT TCG______________________________CTACTACCACCACCACCACCTCTACCACCACT GCTACTACCATCACCACCACCACTACCACCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41544525..41544823 26863196 MeRIP-seq:(Medium) rs1558045359 Functional Loss DEL dbSNP153 4..33 33 - - - 88513 RMVar_ID_88513 Human_SNP_ID_10788207 m1A Human chr1 + 41544659 41544659 41544659 TCGCTACTACCATCACCACCACCACTACCACCACTACTACCACCACCACCACCTCTACCACCACT TCGCTACTACCATCACCACCACCACTACCACCGCTACTACCACCACCACCACCTCTACCACCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41544525..41544823 26863196 MeRIP-seq:(Medium) rs1282603066 Functional Loss SNV dbSNP153 33..33 33 - - - 88514 RMVar_ID_88514 Human_SNP_ID_10788208 m1A Human chr1 + 41544659 41544659 41544659 TCGCTACTACCATCACCACCACCACTACCACCACTACTACCACCACCACCACCTCTACCACCACT TCGCTACTACCATCACCACCACCACTACCACCTCTACTACCACCACCACCACCTCTACCACCACT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41544525..41544823 26863196 MeRIP-seq:(Medium) rs1282603066 Functional Loss SNV dbSNP153 33..33 33 - - - 88515 RMVar_ID_88515 Human_SNP_ID_10788899 m1A Human chr1 - 41545122 41545122 41545122 TGGTGTTGGTGGTGATGGTGGTAGTGGTGATGATGGTAGTGGTGGTGGTGGTGATGGTAGCGATG TGGTGTTGGTGGTGATGGTGGTAGTGGTGATGGTGGTAGTGGTGGTGGTGGTGATGGTAGCGATG T C HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41545044..41545367 26863196 MeRIP-seq:(Medium) rs1215774921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15419 88516 RMVar_ID_88516 Human_SNP_ID_10789279 m1A Human chr1 + 41545634 41545626 41545635 CCACCATCACCACCACTACCATCACCACCACCATCACCACCATCACCACCACTACCACCCCTGCC CCACCATCACCACCACTACCATCAC_________CACCACCATCACCACCACTACCACCCCTGCC CCACCACCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41545435..41545643 26863196 MeRIP-seq:(Medium) rs1172617466 Functional Loss DEL dbSNP153 26..34 33 - - - 88517 RMVar_ID_88517 Human_SNP_ID_10817196 m1A Human chr1 + 41662828 41662828 41662828 GGCCCTGCCACTCTGCGCCACGCCTTGGTCGCACCCGGGCCCAGCGGGAGTCCATCGCCGTCCCC GGCCCTGCCACTCTGCGCCACGCCTTGGTCGCCCCCGGGCCCAGCGGGAGTCCATCGCCGTCCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41662786..41662869 26863196 MeRIP-seq:(Medium) rs1402620429 Functional Loss SNV dbSNP153 33..33 33 - - - 88518 RMVar_ID_88518 Human_SNP_ID_10846026 m1A Human chr1 - 41790846 41790846 41790846 ATGGATGCATCTTGTCCATGGGGCCATGAGGGAGCATGGGATATGCTAGGACAAGTGTTAGGGAC ATGGATGCATCTTGTCCATGGGGCCATGAGGGTGCATGGGATATGCTAGGACAAGTGTTAGGGAC T A HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41790808..41790954 26863196 MeRIP-seq:(Medium) rs1444411046 Functional Loss SNV dbSNP153 33..33 33 - - - 88519 RMVar_ID_88519 Human_SNP_ID_10867998 m1A Human chr1 - 41889025 41889021 41889026 TGTGTGGTGTGTGTGTGTGTGTGTAGCGTGTGAGGTATGTGGTGTGTGTATGTGGTATGTGGTGT TGTGTGGTGTGTGTGTGTGTGTGTAGCGTGT_____ATGTGGTGTGTGTATGTGGTATGTGGTGT TACCTC T HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:41888715..41889223 26863196 MeRIP-seq:(Medium) rs1411961457 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_23395204 88520 RMVar_ID_88520 Human_SNP_ID_10937448 m1A Human chr1 - 42191432 42191432 42191432 CCCCACACCCAGCACCACACCCACAGCAACACAGCCAGCTCCAGTCCCCTCACCCCCAGCATCCC CCCCACACCCAGCACCACACCCACAGCAACACTGCCAGCTCCAGTCCCCTCACCCCCAGCATCCC T A FOXJ3 Ensembl:ENSG00000198815 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:42191382..42191544 26863196 MeRIP-seq:(Medium) rs941033595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17072366,Human_RBP_ID_18928258 Human_miRNA_ID_1230609,Human_miRNA_ID_1558531,Human_miRNA_ID_2329918,Human_miRNA_ID_2962995 RMVar_hsa_circ_12576,RMVar_hsa_circ_47353,RMVar_hsa_circ_50069,RMVar_hsa_circ_266243,RMVar_hsa_circ_326493,RMVar_hsa_circ_354930,RMVar_hsa_circ_49578,RMVar_hsa_circ_101233,RMVar_hsa_circ_132138 88521 RMVar_ID_88521 Human_SNP_ID_10973930 m1A Human chr1 - 42335158 42335158 42335158 CGCCGCCGCTCTCGGGGCTGCTCGGGGCCTCGACCGCTCGCAGTAGGCACCGTTGGGACCTTTCC CGCCGCCGCTCTCGGGGCTGCTCGGGGCCTCGGCCGCTCGCAGTAGGCACCGTTGGGACCTTTCC T C FOXJ3 Ensembl:ENSG00000198815 Protein coding intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1396938238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103312,Human_RBP_ID_4073937,Human_RBP_ID_9318869,Human_RBP_ID_17338165,Human_RBP_ID_18414940 Human_Splice_Rec_55209,Human_Splice_Rec_55231,Human_Splice_Rec_55255 RMVar_hsa_circ_128133,RMVar_hsa_circ_132153 88522 RMVar_ID_88522 Human_SNP_ID_11003268 m1A Human chr1 - 42456630 42456630 42456630 GCGCGCCCAGCCTGGCCGCGAAGCGAGCCATAACCTCAGCCCAGCGCGCAGCACCGGGAGGCTGG GCGCGCCCAGCCTGGCCGCGAAGCGAGCCATAGCCTCAGCCCAGCGCGCAGCACCGGGAGGCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr1:42456582..42456832;chr1:42456603..42456753 26863196,32194978 MeRIP-seq:(Medium) rs770850781 Functional Loss SNV dbSNP153 33..33 33 - - - 88523 RMVar_ID_88523 Human_SNP_ID_11003271 m1A Human chr1 - 42456637 42456637 42456637 CGGCCCTGCGCGCCCAGCCTGGCCGCGAAGCGAGCCATAACCTCAGCCCAGCGCGCAGCACCGGG CGGCCCTGCGCGCCCAGCCTGGCCGCGAAGCGGGCCATAACCTCAGCCCAGCGCGCAGCACCGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:42456587..42456745;chr1:42456586..42456754 26863196 MeRIP-seq:(Medium) rs1209740267 Functional Loss SNV dbSNP153 33..33 33 - - - 88524 RMVar_ID_88524 Human_SNP_ID_11003289 m1A Human chr1 - 42456654 42456654 42456654 TAACCAACACCACCCGCCGGCCCTGCGCGCCCAGCCTGGCCGCGAAGCGAGCCATAACCTCAGCC TAACCAACACCACCCGCCGGCCCTGCGCGCCCTGCCTGGCCGCGAAGCGAGCCATAACCTCAGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42456606..42456706 26863196 MeRIP-seq:(Medium) rs1217355949 Functional Loss SNV dbSNP153 33..33 33 - - - 88525 RMVar_ID_88525 Human_SNP_ID_11003337 m1A Human chr1 - 42456770 42456770 42456770 CCCGTAGCCGGCGGCTAGGAAGGCCTCGGCCGAGGTTGCACCGCGCCGCCCGCTGCTGAAGTTGT CCCGTAGCCGGCGGCTAGGAAGGCCTCGGCCGGGGTTGCACCGCGCCGCCCGCTGCTGAAGTTGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:42456591..42456826 26863410 MeRIP-seq:(Medium) rs1156505243 Functional Loss SNV dbSNP153 33..33 33 - - - 88526 RMVar_ID_88526 Human_SNP_ID_11006384 m1A Human chr1 - 42468980 42468980 42468980 CTGTGATGTCACTTTCTCCTGTTTTGACTCCTATGTCTCTAGCCTTTCCTTCTCAGTATGCTTCC CTGTGATGTCACTTTCTCCTGTTTTGACTCCTGTGTCTCTAGCCTTTCCTTCTCAGTATGCTTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:42468929..42469061 26863196 MeRIP-seq:(Medium) rs1329706961 Functional Loss SNV dbSNP153 33..33 33 - - - 88527 RMVar_ID_88527 Human_SNP_ID_11053670 m1A Human chr1 - 42682502 42682502 42682502 GGCAGCTGCGGCTCCTCCCGGGGTGTGATGGTAACTAGGCCGGCGGCGGCGGTGGGGCTGCTCAG GGCAGCTGCGGCTCCTCCCGGGGTGTGATGGTGACTAGGCCGGCGGCGGCGGTGGGGCTGCTCAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:42682451..42682650 26863196 MeRIP-seq:(Medium) rs1029199226 Functional Loss SNV dbSNP153 33..33 33 - - - 88528 RMVar_ID_88528 Human_SNP_ID_11054191 m1A Human chr1 - 42683292 42683292 42683292 CCCTCGCACGCCGGCCGCCGCGGCCACCTGACAGCCCTTTCTCTCCACCGCCCGGGTGCGGGGCC CCCTCGCACGCCGGCCGCCGCGGCCACCTGACTGCCCTTTCTCTCCACCGCCCGGGTGCGGGGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:42683289..42683475 26863196 MeRIP-seq:(Medium) rs763567010 Functional Loss SNV dbSNP153 33..33 33 - - - 88529 RMVar_ID_88529 Human_SNP_ID_11054269 m1A Human chr1 + 42683405 42683405 42683405 TGGCTTGTTTTGCTTTGTTTTCTTTTCCAGCAACGAAGGTTTTGGGAACAGTAAAATGGTTCAAT TGGCTTGTTTTGCTTTGTTTTCTTTTCCAGCAGCGAAGGTTTTGGGAACAGTAAAATGGTTCAAT A G YBX1 Ensembl:ENSG00000065978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42683401..42683475 26863196 MeRIP-seq:(Medium) rs772779381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17325,Human_RBP_ID_741544,Human_RBP_ID_800796,Human_RBP_ID_859388,Human_RBP_ID_1255869,Human_RBP_ID_1748365,Human_RBP_ID_18187698,Human_RBP_ID_24699251,Human_RBP_ID_27594913 Human_Splice_Rec_56414,Human_Splice_Rec_56415,Human_Splice_Rec_56428,Human_Splice_Rec_56429,Human_Splice_Rec_56447 RMVar_hsa_circ_58394,RMVar_hsa_circ_109677,RMVar_hsa_circ_96779,RMVar_hsa_circ_118671,RMVar_hsa_circ_132185,RMVar_hsa_circ_132186,RMVar_hsa_circ_125874,RMVar_hsa_circ_71356,RMVar_hsa_circ_132187,RMVar_hsa_circ_132188 88530 RMVar_ID_88530 Human_SNP_ID_11057533 m1A Human chr1 + 42696154 42696154 42696154 TTGACTCTGGTACATTTTAAATGAAAAAGCACATTATTCTCCCCTGTTAATCTATTTTTGGAATG TTGACTCTGGTACATTTTAAATGAAAAAGCACGTTATTCTCCCCTGTTAATCTATTTTTGGAATG A G YBX1 Ensembl:ENSG00000065978 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:42696151..42696228 26863196 MeRIP-seq:(Medium) rs955734597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1748409,Human_RBP_ID_2148349,Human_RBP_ID_17588035,Human_RBP_ID_22535179,Human_RBP_ID_24699384 RMVar_hsa_circ_58394,RMVar_hsa_circ_118671,RMVar_hsa_circ_132186,RMVar_hsa_circ_125874,RMVar_hsa_circ_71356,RMVar_hsa_circ_132188,RMVar_hsa_circ_300896 88531 RMVar_ID_88531 Human_SNP_ID_11057556 m1A Human chr1 - 42696276 42696276 42696276 TACACAAAAAGCATCCTCACCTTTTCTCCTTCAACAACATCAAACTCCACAGTCTCTCCATCTCC TACACAAAAAGCATCCTCACCTTTTCTCCTTCGACAACATCAAACTCCACAGTCTCTCCATCTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42696251..42696275 26863196 MeRIP-seq:(Medium) rs200026917 Functional Loss SNV dbSNP153 33..33 33 - - - 88532 RMVar_ID_88532 Human_SNP_ID_11057731 m1A Human chr1 + 42696741 42696741 42696741 ACCGTAACCATTATAGACGCTATCCACGTCGTAGGGGTCCTCCACGCAATTACCAGCAAAATTAC ACCGTAACCATTATAGACGCTATCCACGTCGTGGGGGTCCTCCACGCAATTACCAGCAAAATTAC A G YBX1 Ensembl:ENSG00000065978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42696626..42696800 26863196 MeRIP-seq:(Medium) rs765100312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_355628,Human_RBP_ID_978423,Human_RBP_ID_1431736,Human_RBP_ID_1748415,Human_RBP_ID_3313680,Human_RBP_ID_4053449,Human_RBP_ID_5827212,Human_RBP_ID_8311702,Human_RBP_ID_8749549,Human_RBP_ID_8970317,Human_RBP_ID_10994040,Human_RBP_ID_17218699,Human_RBP_ID_17335949,Human_RBP_ID_17751673,Human_RBP_ID_18187073,Human_RBP_ID_18430412,Human_RBP_ID_18575377,Human_RBP_ID_22864312,Human_RBP_ID_26798250,Human_RBP_ID_26865009,Human_RBP_ID_27183505,Human_RBP_ID_27398935,Human_RBP_ID_27594958 Human_Splice_Rec_56420,Human_Splice_Rec_56432,Human_Splice_Rec_56440,Human_Splice_Rec_56452 RMVar_hsa_circ_58394,RMVar_hsa_circ_118671,RMVar_hsa_circ_132186,RMVar_hsa_circ_125874,RMVar_hsa_circ_71356,RMVar_hsa_circ_132188,RMVar_hsa_circ_300896,RMVar_hsa_circ_301963,RMVar_hsa_circ_132190,RMVar_hsa_circ_118994,RMVar_hsa_circ_132189,RMVar_hsa_circ_124394,RMVar_hsa_circ_266656,RMVar_hsa_circ_132192 88533 RMVar_ID_88533 Human_SNP_ID_11058847 m1A Human chr1 + 42700796 42700796 42700796 GACACCGTTCATTGCAGGGGCCCTCCTCGCCAAAGACAGCCTAGAGAGGACGGCAATGAAGAAGA GACACCGTTCATTGCAGGGGCCCTCCTCGCCAGAGACAGCCTAGAGAGGACGGCAATGAAGAAGA A G YBX1 Ensembl:ENSG00000065978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42700776..42701025 26863196 MeRIP-seq:(Medium) rs760131332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9356194 Human_Splice_Rec_56424,Human_Splice_Rec_56444 Human_miRNA_ID_2569838 RMVar_hsa_circ_118671,RMVar_hsa_circ_132186,RMVar_hsa_circ_71356,RMVar_hsa_circ_300896,RMVar_hsa_circ_132190,RMVar_hsa_circ_118994 88534 RMVar_ID_88534 Human_SNP_ID_11076708 m1A Human chr1 + 42766754 42766754 42766754 GGAAGTCGGCGGCACACTGGGTGCGGCAGCGCAGGCGAAGGGCGCGGAGGGCTGCCCGGGAGCGC GGAAGTCGGCGGCACACTGGGTGCGGCAGCGCGGGCGAAGGGCGCGGAGGGCTGCCCGGGAGCGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:42766635..42766950 32194978 MeRIP-seq:(Medium) rs1432203483 Functional Loss SNV dbSNP153 33..33 33 - - - 88535 RMVar_ID_88535 Human_SNP_ID_11076812 m1A Human chr1 - 42766963 42766963 42766963 GGTTCCGTTAGGTCTGAGGGAGCGATGGCGGTACGCGCGTTGAAGCTGCTGACCACACTGCTGGC GGTTCCGTTAGGTCTGAGGGAGCGATGGCGGTGCGCGCGTTGAAGCTGCTGACCACACTGCTGGC T C P3H1 Ensembl:ENSG00000117385 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42766710..42767025 26863196 MeRIP-seq:(Medium) rs1300737039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072752,Human_RBP_ID_5311679,Human_RBP_ID_5458325,Human_RBP_ID_18468555,Human_RBP_ID_22023276,Human_RBP_ID_22429295 88536 RMVar_ID_88536 Human_SNP_ID_11076994 m1A Human chr1 + 42767319 42767319 42767319 GGAGTGGGGAGGATAAGGCGCTGTCATGGAGGACGCCGCCGCGCCGGGGCGGACCGAGGGGGTCC GGAGTGGGGAGGATAAGGCGCTGTCATGGAGGGCGCCGCCGCGCCGGGGCGGACCGAGGGGGTCC A G AC098484.3,C1orf50 Ensembl:ENSG00000283580,Ensembl:ENSG00000164008 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42767268..42773614 26863196 MeRIP-seq:(Medium) rs1402287610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073942,Human_RBP_ID_17762574,Human_RBP_ID_18415518 Human_Splice_Rec_56657,Human_Splice_Rec_56673,Human_Splice_Rec_56683 88537 RMVar_ID_88537 Human_SNP_ID_11088755 m1A Human chr1 - 42816563 42816563 42816563 TTCTGTACCACCCAGATCAGAGCCTCCTAAGAAATATCCAGAAGTCAAGCCATGGATCCACCTGC TTCTGTACCACCCAGATCAGAGCCTCCTAAGACATATCCAGAAGTCAAGCCATGGATCCACCTGC T G SVBP Ensembl:ENSG00000177868 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42816470..42824455 26863196 MeRIP-seq:(Medium) rs370680427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_978433,Human_RBP_ID_4073943 Human_Splice_Rec_56742,Human_Splice_Rec_56746,Human_Splice_Rec_56750 88538 RMVar_ID_88538 Human_SNP_ID_11089015 m1A Human chr1 - 42817279 42817279 42817279 ACGAGGGGCGGTGGGCAGGCAGCGCTGGGTCCAGTGGTCGGGGGAAGGCGAGGATTACCCTCCCG ACGAGGGGCGGTGGGCAGGCAGCGCTGGGTCCGGTGGTCGGGGGAAGGCGAGGATTACCCTCCCG T C SVBP Ensembl:ENSG00000177868 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:42817265..42817355 26863410 MeRIP-seq:(Medium) rs1227636493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_56745,Human_Splice_Rec_56749 88539 RMVar_ID_88539 Human_SNP_ID_11089020 m1A Human chr1 + 42817282 42817282 42817282 GAGGGTAATCCTCGCCTTCCCCCGACCACTGGACCCAGCGCTGCCTGCCCACCGCCCCTCGTCCT GAGGGTAATCCTCGCCTTCCCCCGACCACTGGCCCCAGCGCTGCCTGCCCACCGCCCCTCGTCCT A C ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:42817176..42817325 26863410 MeRIP-seq:(Medium) rs989877919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18575462 88540 RMVar_ID_88540 Human_SNP_ID_11089021 m1A Human chr1 + 42817282 42817282 42817282 GAGGGTAATCCTCGCCTTCCCCCGACCACTGGACCCAGCGCTGCCTGCCCACCGCCCCTCGTCCT GAGGGTAATCCTCGCCTTCCCCCGACCACTGGTCCCAGCGCTGCCTGCCCACCGCCCCTCGTCCT A T ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:42817176..42817325 26863410 MeRIP-seq:(Medium) rs989877919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18575462 88541 RMVar_ID_88541 Human_SNP_ID_11089025 m1A Human chr1 + 42817286 42817286 42817286 GTAATCCTCGCCTTCCCCCGACCACTGGACCCAGCGCTGCCTGCCCACCGCCCCTCGTCCTGGGC GTAATCCTCGCCTTCCCCCGACCACTGGACCCCGCGCTGCCTGCCCACCGCCCCTCGTCCTGGGC A C ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:42816769..42817354 26863196 MeRIP-seq:(Medium) rs1210195992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18575462 88542 RMVar_ID_88542 Human_SNP_ID_11089035 m1A Human chr1 - 42817295 42817295 42817295 CGCGGCCCCGCCCAGGACGAGGGGCGGTGGGCAGGCAGCGCTGGGTCCAGTGGTCGGGGGAAGGC CGCGGCCCCGCCCAGGACGAGGGGCGGTGGGCCGGCAGCGCTGGGTCCAGTGGTCGGGGGAAGGC T G SVBP Ensembl:ENSG00000177868 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:42817209..42817325 26863410 MeRIP-seq:(Medium) rs886290893 Functional Loss SNV dbSNP153 33..33 33 - - - 88543 RMVar_ID_88543 Human_SNP_ID_11089070 m1A Human chr1 + 42817346 42817346 42817346 TGGGCGGGGCCGCGCGCCGGGGGGAGGGGCGCAGGGCCGAGCGCCAGGAGGCTTCCGCCCGCAGG TGGGCGGGGCCGCGCGCCGGGGGGAGGGGCGCGGGGCCGAGCGCCAGGAGGCTTCCGCCCGCAGG A G ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:42817260..42817352 26863410 MeRIP-seq:(Medium) rs956217235 Functional Loss SNV dbSNP153 33..33 33 - - - 88544 RMVar_ID_88544 Human_SNP_ID_11095818 m1A Human chr1 - 42847062 42847062 42847062 GGAAGCAAAGGCTGCCAGAAGTGTCACAGGCCAGGGCCCAAGAGCTGAGTTGTGTGTTGCGGGGC GGAAGCAAAGGCTGCCAGAAGTGTCACAGGCCGGGGCCCAAGAGCTGAGTTGTGTGTTGCGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42847060..42847180 26863196 MeRIP-seq:(Medium) rs979875308 Functional Loss SNV dbSNP153 33..33 33 - - - 88545 RMVar_ID_88545 Human_SNP_ID_11096518 m1A Human chr1 + 42850001 42850001 42850001 GTATATGTGTATAGACATGTATGTAGCTATATATGTGTGTGGCTGTGGTATGTGGCTATATGTGG GTATATGTGTATAGACATGTATGTAGCTATATGTGTGTGTGGCTGTGGTATGTGGCTATATGTGG A G ZNF691 Ensembl:ENSG00000164011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42849999..42850212 26863196 MeRIP-seq:(Medium) rs1341385158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1073389,Human_RBP_ID_23395942,Human_RBP_ID_27835633 88546 RMVar_ID_88546 Human_SNP_ID_11096544 m1A Human chr1 - 42850121 42850121 42850121 CTCACATACCTGACATACTCGGTCACATTCTCATACCACACACAACAGCTATACACCTACACACC CTCACATACCTGACATACTCGGTCACATTCTCGTACCACACACAACAGCTATACACCTACACACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:42850117..42850201 26863196 MeRIP-seq:(Medium) rs114831725 Functional Loss SNV dbSNP153 33..33 33 - - - 88547 RMVar_ID_88547 Human_SNP_ID_11096756 m1A Human chr1 + 42850971 42850968 42850971 TTCATTCTCAGGGTTCAGAGATGGGCAGTGAGAAGGAGCAGAGTCCAGAACCACACCTGCCTGAG TTCATTCTCAGGGTTCAGAGATGGGCAGTG___AGGAGCAGAGTCCAGAACCACACCTGCCTGAG GAGA G ZNF691 Ensembl:ENSG00000164011 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42850966..42851090 26863196 MeRIP-seq:(Medium) rs1299584907 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23395966 Human_Splice_Rec_56902,Human_Splice_Rec_56904,Human_Splice_Rec_56910,Human_Splice_Rec_56914,Human_Splice_Rec_56920,Human_Splice_Rec_56928,Human_Splice_Rec_56934,Human_Splice_Rec_56936,Human_Splice_Rec_56938 RMVar_hsa_circ_100577,RMVar_hsa_circ_132217 88548 RMVar_ID_88548 Human_SNP_ID_11096979 m1A Human chr1 - 42851583 42851583 42851583 TGTGTGGGTGCGGTGATGCACGCCAAAGCTGGAGCTGTTGCTGAAGCTCTTCCCACACTCACAGC TGTGTGGGTGCGGTGATGCACGCCAAAGCTGGTGCTGTTGCTGAAGCTCTTCCCACACTCACAGC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:42851533..42851633 32194978 MeRIP-seq:(Medium) rs1433994144 Functional Loss SNV dbSNP153 33..33 33 - - - 88549 RMVar_ID_88549 Human_SNP_ID_11096980 m1A Human chr1 - 42851583 42851583 42851583 TGTGTGGGTGCGGTGATGCACGCCAAAGCTGGAGCTGTTGCTGAAGCTCTTCCCACACTCACAGC TGTGTGGGTGCGGTGATGCACGCCAAAGCTGGCGCTGTTGCTGAAGCTCTTCCCACACTCACAGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:42851533..42851633 32194978 MeRIP-seq:(Medium) rs1433994144 Functional Loss SNV dbSNP153 33..33 33 - - - 88550 RMVar_ID_88550 Human_SNP_ID_11115917 m1A Human chr1 + 42927172 42927172 42927172 GAAGGTCCGGCCTTTAGTCTCAGGAACTTTGAAGTAGGTGAAGATGAAGAACAGAACCAGGAGCA GAAGGTCCGGCCTTTAGTCTCAGGAACTTTGAGGTAGGTGAAGATGAAGAACAGAACCAGGAGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:42927121..42927249 26863196 MeRIP-seq:(Medium) rs1216296247 Functional Loss SNV dbSNP153 33..33 33 - - - 88551 RMVar_ID_88551 Human_SNP_ID_11116848 m1A Human chr1 + 42929951 42929951 42929951 GGGACTCTCGGGGCAGAAGGGCAGCACGATGCACTGCAGCAGGGCCGGGATGAAGATGATGCTCA GGGACTCTCGGGGCAGAAGGGCAGCACGATGCCCTGCAGCAGGGCCGGGATGAAGATGATGCTCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:42929901..42930050 32194978 MeRIP-seq:(Medium) rs1050933017 Functional Loss SNV dbSNP153 33..33 33 - - - 88552 RMVar_ID_88552 Human_SNP_ID_11117583 m1A Human chr1 - 42932288 42932288 42932288 AACGGGTGCTGCCTGCCTACCACATCCGTGGGAGCTGGCCAGGGTGGGGGCAGGGCTGGTGGGCA AACGGGTGCTGCCTGCCTACCACATCCGTGGGCGCTGGCCAGGGTGGGGGCAGGGCTGGTGGGCA T G SLC2A1 Ensembl:ENSG00000117394 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42932284..42932397 26863196 MeRIP-seq:(Medium) rs1344249116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167000 RMVar_hsa_circ_105272,RMVar_hsa_circ_132221,RMVar_hsa_circ_26250 88553 RMVar_ID_88553 Human_SNP_ID_11118172 m1A Human chr1 - 42934745 42934745 42934745 TGGGACGGGCATGTGAGGTGGGAGCGTTCAGAACAGGCACGTGCCAGGTCTCACCTCACACATGA TGGGACGGGCATGTGAGGTGGGAGCGTTCAGAGCAGGCACGTGCCAGGTCTCACCTCACACATGA T C SLC2A1 Ensembl:ENSG00000117394 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:42934743..42935034 26863196 MeRIP-seq:(Medium) rs561516617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105272,RMVar_hsa_circ_132221,RMVar_hsa_circ_26250 88554 RMVar_ID_88554 Human_SNP_ID_11118930 m1A Human chr1 + 42938257 42938257 42938257 TCTTCTGCTCTGTCCTCCTCCTCCAGGAGGGGATGCATGGCAGGAATGTCCTGTCACACTCACAG TCTTCTGCTCTGTCCTCCTCCTCCAGGAGGGGGTGCATGGCAGGAATGTCCTGTCACACTCACAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:42938255..42938368 32194978 MeRIP-seq:(Medium) rs1213449116 Functional Loss SNV dbSNP153 33..33 33 - - - 88555 RMVar_ID_88555 Human_SNP_ID_11119596 m1A Human chr1 - 42941232 42941232 42941232 GGGCCCAGCTAGGGAGCATGGACTTCAGGATGAGGACAATAGGGACCCACTGCCCAGGGCAGACG GGGCCCAGCTAGGGAGCATGGACTTCAGGATGGGGACAATAGGGACCCACTGCCCAGGGCAGACG T C SLC2A1 Ensembl:ENSG00000117394 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:42941227..42941298 26863196 MeRIP-seq:(Medium) rs1351692206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5158466,Human_RBP_ID_10995666,Human_RBP_ID_17182410 RMVar_hsa_circ_105272,RMVar_hsa_circ_132221,RMVar_hsa_circ_26250 88556 RMVar_ID_88556 Human_SNP_ID_11120087 m1A Human chr1 - 42943320 42943311 42943321 GCCTATAACAGTGTGGTTTGTTTCTCCGCAGAAGCTGACGGGTCGCCTCATGCTGGCCGTGGGAG GCCTATAACAGTGTGGTTTGTTTCTCCGCAG__________GTCGCCTCATGCTGGCCGTGGGAG CCCGTCAGCTT C SLC2A1 Ensembl:ENSG00000117394 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42943226..42943325 26863196 MeRIP-seq:(Medium) rs587784393 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_849927,Human_RBP_ID_4053736,Human_RBP_ID_22428339,Human_RBP_ID_22633553 Human_Splice_Rec_56940,Human_Splice_Rec_56941,Human_Splice_Rec_56958,Human_Splice_Rec_56959,Human_Splice_Rec_56973,Human_Splice_Rec_56982,Human_Splice_Rec_56983,Human_Splice_Rec_56992,Human_Splice_Rec_56993,Human_Splice_Rec_56996 Clinvar_Rec_499 RMVar_hsa_circ_105272,RMVar_hsa_circ_132221,RMVar_hsa_circ_26250 88557 RMVar_ID_88557 Human_SNP_ID_11120090 m1A Human chr1 - 42943323 42943323 42943323 CACGCCTATAACAGTGTGGTTTGTTTCTCCGCAGAAGCTGACGGGTCGCCTCATGCTGGCCGTGG CACGCCTATAACAGTGTGGTTTGTTTCTCCGCGGAAGCTGACGGGTCGCCTCATGCTGGCCGTGG T C SLC2A1 Ensembl:ENSG00000117394 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr1:42943287..42943375;chr1:42943301..42943392;chr1:42943276..42943325 26863196,32194978 MeRIP-seq:(Medium) rs796053272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_849927,Human_RBP_ID_22633553 Human_Splice_Rec_56941,Human_Splice_Rec_56959,Human_Splice_Rec_56973,Human_Splice_Rec_56983,Human_Splice_Rec_56993 Clinvar_Rec_500 88558 RMVar_ID_88558 Human_SNP_ID_11124052 m1A Human chr1 + 42958628 42958628 42958628 TTGTTCCTGGCGGGAGGGCCCGCGGGCGCGCGACTCACCTTGCTGCTGGGCTCCATGGCAGCGCT TTGTTCCTGGCGGGAGGGCCCGCGGGCGCGCGGCTCACCTTGCTGCTGGGCTCCATGGCAGCGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:42958626..42958675 32194978 MeRIP-seq:(Medium) rs1213322422 Functional Loss SNV dbSNP153 33..33 33 - - - 88559 RMVar_ID_88559 Human_SNP_ID_11124118 m1A Human chr1 - 42958814 42958814 42958814 CGAGCGTGCCGGTCGCTAGTCGCGGGTCCCCGAGTGAGCACGCCAGGGAGCAGGAGACCAAACGA CGAGCGTGCCGGTCGCTAGTCGCGGGTCCCCGTGTGAGCACGCCAGGGAGCAGGAGACCAAACGA T A SLC2A1 Ensembl:ENSG00000117394 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr1:42958626..42958875 26863196 MeRIP-seq:(Medium) rs1014539595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223752,Human_RBP_ID_4072760,Human_RBP_ID_5311681,Human_RBP_ID_22428342,Human_RBP_ID_23395990 RMVar_hsa_circ_132222 88560 RMVar_ID_88560 Human_SNP_ID_11124251 m1A Human chr1 - 42959162 42959162 42959162 TTACAGCCGGGTACCGGCTCCACCATTTTGCTAGAGAAGGCCGCGGAGGCTCAGAGAGGTGCGCA TTACAGCCGGGTACCGGCTCCACCATTTTGCTCGAGAAGGCCGCGGAGGCTCAGAGAGGTGCGCA T G AC099795.1 Ensembl:ENSG00000283973 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:42959111..42959207 26863196 MeRIP-seq:(Medium) rs1474717382 Functional Loss SNV dbSNP153 33..33 33 - - - 88561 RMVar_ID_88561 Human_SNP_ID_11150039 m1A Human chr1 + 43067132 43067128 43067132 CTTGAGGGACTGGTAGAGACTGGGGAGAGAAGAAAGAGGCAGGGTGTTCTAGGCAGGAAGATCAG CTTGAGGGACTGGTAGAGACTGGGGAGAG____AAGAGGCAGGGTGTTCTAGGCAGGAAGATCAG GAAGA G SLC2A1-AS1 RNACentral:URS0000D56D25 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43067012..43067214 26863196 MeRIP-seq:(Medium) rs1456661713 Functional Loss DEL dbSNP153 30..33 33 - - - 88562 RMVar_ID_88562 Human_SNP_ID_11173884 m1A Human chr1 + 43165494 43165494 43165494 ACCCAATTCAATTACTGAGTCCTGCTCATTTCACCTCTTAAATGTTTCTTCAATCCTTATCTCGA ACCCAATTCAATTACTGAGTCCTGCTCATTTCCCCTCTTAAATGTTTCTTCAATCCTTATCTCGA A C SLC2A1-AS1 RNACentral:URS0000D56D25 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43165492..43165689 26863196 MeRIP-seq:(Medium) rs1030160054 Functional Loss SNV dbSNP153 33..33 33 - - - 88563 RMVar_ID_88563 Human_SNP_ID_11175513 m1A Human chr1 + 43172140 43172140 43172140 GGAGTGTCCATCTCGCCGCACGCACGTCCCACACCTACAGGAAGAAACGGGGTATCCCGAGACCC GGAGTGTCCATCTCGCCGCACGCACGTCCCACGCCTACAGGAAGAAACGGGGTATCCCGAGACCC A G SLC2A1-AS1 RNACentral:URS0000D56D25 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:43172051..43172286 26863196 MeRIP-seq:(Medium) rs755797119 Functional Loss SNV dbSNP153 33..33 33 - - - 88564 RMVar_ID_88564 Human_SNP_ID_11175530 m1A Human chr1 + 43172174 43172174 43172174 CTACAGGAAGAAACGGGGTATCCCGAGACCCAAGCGGCTAGCAGAGGGCGGCCCTGGCCGCTGCT CTACAGGAAGAAACGGGGTATCCCGAGACCCAGGCGGCTAGCAGAGGGCGGCCCTGGCCGCTGCT A G CFAP57 Ensembl:ENSG00000243710 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43172051..43172273 32194978 MeRIP-seq:(Medium) rs11559314 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11160,GWAS_ID_11161,GWAS_ID_11162 88565 RMVar_ID_88565 Human_SNP_ID_11175548 m1A Human chr1 - 43172237 43172237 43172237 GGCGCTGGAGCGATTCGGTGGCACGTGGAGCCACGGCGTGGGAGTAGGGGGCTGAAGGCAGGCAG GGCGCTGGAGCGATTCGGTGGCACGTGGAGCCTCGGCGTGGGAGTAGGGGGCTGAAGGCAGGCAG T A EBNA1BP2 Ensembl:ENSG00000117395 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43171793..43172300;chr1:43171876..43172300 26863196 MeRIP-seq:(Medium) rs1241225823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24484,Human_RBP_ID_100643,Human_RBP_ID_223756,Human_RBP_ID_744751,Human_RBP_ID_4053800,Human_RBP_ID_5458503,Human_RBP_ID_9270111,Human_RBP_ID_18414942,Human_RBP_ID_22428344,Human_RBP_ID_22871774,Human_RBP_ID_23205140,Human_RBP_ID_23396102,Human_RBP_ID_26309740 88566 RMVar_ID_88566 Human_SNP_ID_11175551 m1A Human chr1 - 43172241 43172241 43172241 TGCTGGCGCTGGAGCGATTCGGTGGCACGTGGAGCCACGGCGTGGGAGTAGGGGGCTGAAGGCAG TGCTGGCGCTGGAGCGATTCGGTGGCACGTGGGGCCACGGCGTGGGAGTAGGGGGCTGAAGGCAG T C EBNA1BP2 Ensembl:ENSG00000117395 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:43172034..43172300 26863196 MeRIP-seq:(Medium) rs1473024800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24484,Human_RBP_ID_100643,Human_RBP_ID_223756,Human_RBP_ID_744751,Human_RBP_ID_4073946,Human_RBP_ID_5458503,Human_RBP_ID_9270111,Human_RBP_ID_18414942,Human_RBP_ID_22428344,Human_RBP_ID_22871774,Human_RBP_ID_23205140,Human_RBP_ID_26309740 88567 RMVar_ID_88567 Human_SNP_ID_11175592 m1A Human chr1 + 43172291 43172291 43172291 GCTCCAGCGCCAGCAACTCACAGCTACTGCTCAACTTTTGATTGGGACTTCCGCTTCCGGCGGCA GCTCCAGCGCCAGCAACTCACAGCTACTGCTCTACTTTTGATTGGGACTTCCGCTTCCGGCGGCA A T CFAP57 Ensembl:ENSG00000243710 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43172272..43172371 32194978 MeRIP-seq:(Medium) rs1334652289 Functional Loss SNV dbSNP153 33..33 33 - - - 88568 RMVar_ID_88568 Human_SNP_ID_11206982 m1A Human chr1 - 43305345 43305300 43305346 TACCCTCCCCACCAGTTCAAATGCCCCTCTTTACCGTTGCTCTTCCAGATCACGTCTGTCTGCTT TACCCTCCCCACCAGTTCAAATGCCCCTCTT__________________________________ TGTGCACAAGGAGAAGCAGACAGACGTGATCTGGAAGAGCAACGGTA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43305298..43309084 32194978 MeRIP-seq:(Medium) rs1553122864 Functional Loss DEL dbSNP153 32..65 33 - - - 88569 RMVar_ID_88569 Human_SNP_ID_11217918 m1A Human chr1 - 43349696 43349696 43349696 AGTGAGTCAGGTCGTGTCTGTAGGGCTAGAGAAAGGGGGCCATTGTTTGGACTAGGTTTAGGAGG AGTGAGTCAGGTCGTGTCTGTAGGGCTAGAGATAGGGGGCCATTGTTTGGACTAGGTTTAGGAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43349645..43349710 26863196 MeRIP-seq:(Medium) rs535165133 Functional Loss SNV dbSNP153 33..33 33 - - - 88570 RMVar_ID_88570 Human_SNP_ID_11220436 m1A Human chr1 + 43359189 43359189 43359189 TTTCCTCCAGGGCTCCGTAGGCACCAACTGCAAGGACCCCTCCCCCTGCGGGCGCTCCCATGGCA TTTCCTCCAGGGCTCCGTAGGCACCAACTGCAGGGACCCCTCCCCCTGCGGGCGCTCCCATGGCA A G CDC20 Ensembl:ENSG00000117399 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43358951..43359395;chr1:43358951..43359409;chr1:43358976..43359400 26863196 MeRIP-seq:(Medium) rs1481135097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851483,Human_RBP_ID_1431803,Human_RBP_ID_3313842,Human_RBP_ID_4053807,Human_RBP_ID_5311682,Human_RBP_ID_5335312,Human_RBP_ID_5457693,Human_RBP_ID_5827862,Human_RBP_ID_8754958,Human_RBP_ID_26865131 Human_Splice_Rec_57496 Human_miRNA_ID_2152696,Human_miRNA_ID_2800567,Human_miRNA_ID_3008695 RMVar_hsa_circ_32296,RMVar_hsa_circ_82216,RMVar_hsa_circ_125335,RMVar_hsa_circ_132236,RMVar_hsa_circ_45295,RMVar_hsa_circ_132237,RMVar_hsa_circ_23551 88571 RMVar_ID_88571 Human_SNP_ID_11220490 m1A Human chr1 + 43359301 43359301 43359301 ACCCATCCCCAATGCACCCCCTGCGCGCTGGCAGCGCAAAGCCAAGGAAGCCGCAGGCCCGGCCC ACCCATCCCCAATGCACCCCCTGCGCGCTGGCGGCGCAAAGCCAAGGAAGCCGCAGGCCCGGCCC A G CDC20 Ensembl:ENSG00000117399 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:43359250..43359412 26863196 MeRIP-seq:(Medium) rs758653830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742191,Human_RBP_ID_22531952 Human_Splice_Rec_57497,Human_Splice_Rec_57515 Human_miRNA_ID_2216620 RMVar_hsa_circ_32296,RMVar_hsa_circ_82216,RMVar_hsa_circ_125335,RMVar_hsa_circ_132236,RMVar_hsa_circ_45295,RMVar_hsa_circ_132237,RMVar_hsa_circ_23551 88572 RMVar_ID_88572 Human_SNP_ID_11220517 m1A Human chr1 + 43359375 43359375 43359375 TGCGGGCCGCCAACCGATCCCACAGCGCCGGCAGGACTCCGGGCCGAACTCCTGGTCAGTGAGGT TGCGGGCCGCCAACCGATCCCACAGCGCCGGCGGGACTCCGGGCCGAACTCCTGGTCAGTGAGGT A G CDC20 Ensembl:ENSG00000117399 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43359176..43359400 32194978 MeRIP-seq:(Medium) rs1229530921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17218718,Human_RBP_ID_19034686,Human_RBP_ID_22488226,Human_RBP_ID_27399022 Human_Splice_Rec_57497,Human_Splice_Rec_57515 RMVar_hsa_circ_32296,RMVar_hsa_circ_82216,RMVar_hsa_circ_125335,RMVar_hsa_circ_132236,RMVar_hsa_circ_45295,RMVar_hsa_circ_132237,RMVar_hsa_circ_23551 88573 RMVar_ID_88573 Human_SNP_ID_11220586 m1A Human chr1 + 43359582 43359582 43359582 CCCATCGCAGTGCTGCCCAGATGGAGGTGGCCAGCTTCCTCCTGAGCAAGGAGAACCAGCCTGAA CCCATCGCAGTGCTGCCCAGATGGAGGTGGCCGGCTTCCTCCTGAGCAAGGAGAACCAGCCTGAA A G CDC20 Ensembl:ENSG00000117399 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43359476..43359625 32194978 MeRIP-seq:(Medium) rs1432324258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22430521 Human_Splice_Rec_57498,Human_Splice_Rec_57499,Human_Splice_Rec_57516,Human_Splice_Rec_57517 Human_miRNA_ID_2673804,Human_miRNA_ID_2924561,Human_miRNA_ID_3076203 RMVar_hsa_circ_82216,RMVar_hsa_circ_125335,RMVar_hsa_circ_132236,RMVar_hsa_circ_45295,RMVar_hsa_circ_132238,RMVar_hsa_circ_121393,RMVar_hsa_circ_132237,RMVar_hsa_circ_23551,RMVar_hsa_circ_373200,RMVar_hsa_circ_132239 88574 RMVar_ID_88574 Human_SNP_ID_11221624 m1A Human chr1 - 43363053 43363053 43363053 CCTTCTCCCGCTCCCGCCGCCGCGCAGGGTCCAACTCAAAACAGCGCCATAGCCTCAGGGTCTCA CCTTCTCCCGCTCCCGCCGCCGCGCAGGGTCCGACTCAAAACAGCGCCATAGCCTCAGGGTCTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:43362951..43363175;chr1:43362951..43363150 32194978 MeRIP-seq:(Medium) rs1432832386 Functional Loss SNV dbSNP153 33..33 33 - - - 88575 RMVar_ID_88575 Human_SNP_ID_11222294 m1A Human chr1 - 43365172 43365172 43365172 CCTCTACATTGTCTATGAGGTGGGCCCCTGGGATGCCGGGCTTTAATTTCTGTCAGCAGGATAAG CCTCTACATTGTCTATGAGGTGGGCCCCTGGGGTGCCGGGCTTTAATTTCTGTCAGCAGGATAAG T C ELOVL1 Ensembl:ENSG00000066322 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43365166..43365272 26863196 MeRIP-seq:(Medium) rs1557477275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54688 88576 RMVar_ID_88576 Human_SNP_ID_11222430 m1A Human chr1 - 43365583 43365583 43365583 GCCAGGATGGAGGCTGTTGTGAACTTGTACCAAGAGGTGATGAAGCACGCAGGTAAGACGCTATC GCCAGGATGGAGGCTGTTGTGAACTTGTACCAGGAGGTGATGAAGCACGCAGGTAAGACGCTATC T C ELOVL1 Ensembl:ENSG00000066322 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43365576..43365625 26863196 MeRIP-seq:(Medium) rs755573091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1431815,Human_RBP_ID_1748513,Human_RBP_ID_4073951 Human_Splice_Rec_57544,Human_Splice_Rec_57545,Human_Splice_Rec_57558,Human_Splice_Rec_57559,Human_Splice_Rec_57570,Human_Splice_Rec_57571,Human_Splice_Rec_57592,Human_Splice_Rec_57593,Human_Splice_Rec_57606,Human_Splice_Rec_57607,Human_Splice_Rec_57616,Human_Splice_Rec_57617,Human_Splice_Rec_57628,Human_Splice_Rec_57629,Human_Splice_Rec_57642,Human_Splice_Rec_57643,Human_Splice_Rec_57658,Human_Splice_Rec_57659,Human_Splice_Rec_57672,Human_Splice_Rec_57673,Human_Splice_Rec_57692,Human_Splice_Rec_57693,Human_Splice_Rec_57704,Human_Splice_Rec_57705,Human_Splice_Rec_57714,Human_Splice_Rec_57715,Human_Splice_Rec_57722,Human_Splice_Rec_57723 88577 RMVar_ID_88577 Human_SNP_ID_11222483 m1A Human chr1 + 43365830 43365830 43365830 CTGCTCCCCACACATCCTGCTTGCCTGGGAAGAGCTGTTCCACCCTTCCTCTCCACACCTTACTC CTGCTCCCCACACATCCTGCTTGCCTGGGAAGGGCTGTTCCACCCTTCCTCTCCACACCTTACTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43365828..43366396 26863196 MeRIP-seq:(Medium) rs529544830 Functional Loss SNV dbSNP153 33..33 33 - - - 88578 RMVar_ID_88578 Human_SNP_ID_11222905 m1A Human chr1 - 43367514 43367514 43367514 GATTTTCCTGCAGCTTGGGGAGAGGTCCTCCCAGGAGCCTTGGTCCCTCCTGGCCTGCCGGGTGT GATTTTCCTGCAGCTTGGGGAGAGGTCCTCCCCGGAGCCTTGGTCCCTCCTGGCCTGCCGGGTGT T G ELOVL1 Ensembl:ENSG00000066322 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43367512..43367677 26863196 MeRIP-seq:(Medium) rs1348589657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_57543,Human_Splice_Rec_57671,Human_Splice_Rec_57713 88579 RMVar_ID_88579 Human_SNP_ID_11223015 m1A Human chr1 + 43367934 43367934 43367934 GGTCCAGACTCACCCGTAGGGGCCAGGCGGGCAACGGCGGAGCGCTCGGAGGGAGCAGGGCCAGA GGTCCAGACTCACCCGTAGGGGCCAGGCGGGCGACGGCGGAGCGCTCGGAGGGAGCAGGGCCAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43367901..43367975 32194978 MeRIP-seq:(Medium) rs1417088963 Functional Loss SNV dbSNP153 33..33 33 - - - 88580 RMVar_ID_88580 Human_SNP_ID_11224394 m1A Human chr1 - 43373518 43373518 43373518 ATCTGGACCTTCAGTTCCTATTCATAGCTGATACCCCGTGTCTTATTGTCTTTTCCCTCCACTCT ATCTGGACCTTCAGTTCCTATTCATAGCTGATCCCCCGTGTCTTATTGTCTTTTCCCTCCACTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43373502..43373585 26863196 MeRIP-seq:(Medium) rs1007758804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3313855 88581 RMVar_ID_88581 Human_SNP_ID_11226879 m1A Human chr1 - 43385103 43385103 43385103 TAAGATGACTTTTTTAATGTTCCTTTCAGGGAAAATGCCAAGTGGAATAAAAACCAACATCAAGT TAAGATGACTTTTTTAATGTTCCTTTCAGGGAGAATGCCAAGTGGAATAAAAACCAACATCAAGT T C MED8 Ensembl:ENSG00000159479 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43384948..43385712 32194978 MeRIP-seq:(Medium) rs1344724969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2148666,Human_RBP_ID_24699739 Human_Splice_Rec_57738,Human_Splice_Rec_57750,Human_Splice_Rec_57751,Human_Splice_Rec_57764 88582 RMVar_ID_88582 Human_SNP_ID_11227969 m1A Human chr1 - 43389615 43389615 43389615 ACGGCTGATAAGGGAATGTGGGCTGGGGGGCGAGGCTAATTGGAGCGGGAGCGGCGGCGATTAGA ACGGCTGATAAGGGAATGTGGGCTGGGGGGCGCGGCTAATTGGAGCGGGAGCGGCGGCGATTAGA T G MED8 Ensembl:ENSG00000159479 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:43389600..43389759;chr1:43389224..43389762 26863196 MeRIP-seq:(Medium) rs994446940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5827947,Human_RBP_ID_8167015,Human_RBP_ID_23396183,Human_RBP_ID_26773075 88583 RMVar_ID_88583 Human_SNP_ID_11228168 m1A Human chr1 - 43389975 43389975 43389975 CCCGCCCCTCACCTCCGGCTCCGGGCGCTCCGAGGCCATCACACAGCCCTCCCGCGCCGGCCCGG CCCGCCCCTCACCTCCGGCTCCGGGCGCTCCGCGGCCATCACACAGCCCTCCCGCGCCGGCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:43389925..43390022;chr1:43389927..43390053 26863196 MeRIP-seq:(Medium) rs1484505234 Functional Loss SNV dbSNP153 33..33 33 - - - 88584 RMVar_ID_88584 Human_SNP_ID_11235191 m1A Human chr1 - 43418792 43418792 43418792 AGACTGCCAGGCCTTGAACCTCTGCTCTCTCCAAATCTATCCACATTGTCCTGACCCTCCTTTCT AGACTGCCAGGCCTTGAACCTCTGCTCTCTCCGAATCTATCCACATTGTCCTGACCCTCCTTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43418748..43418838 26863196 MeRIP-seq:(Medium) rs930121777 Functional Loss SNV dbSNP153 33..33 33 - - - 88585 RMVar_ID_88585 Human_SNP_ID_11236633 m1A Human chr1 + 43423531 43423530 43423531 CTTAGCAGGGTATGAGTGGTACGGAGGTGTGGAAGGGCGTGGCTTAGTGGGGTATGAGTGGTACA CTTAGCAGGGTATGAGTGGTACGGAGGTGTGG_AGGGCGTGGCTTAGTGGGGTATGAGTGGTACA GA G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43423358..43424171 26863196 MeRIP-seq:(Medium) rs1288766678 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_804125,Human_RBP_ID_5641645,Human_RBP_ID_8167016 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88586 RMVar_ID_88586 Human_SNP_ID_11236754 m1A Human chr1 + 43423795 43423794 43423796 GAGTAGGTCAGAGGTGTGGAAGGGTGTGACTTAGGGGGGTATGAGTGATACAGAGGTATGGAAGG GAGTAGGTCAGAGGTGTGGAAGGGTGTGACTT__GGGGGTATGAGTGATACAGAGGTATGGAAGG TAG T SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43423757..43423903 26863196 MeRIP-seq:(Medium) rs1301963682 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23396202 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88587 RMVar_ID_88587 Human_SNP_ID_11236755 m1A Human chr1 + 43423795 43423794 43423795 GAGTAGGTCAGAGGTGTGGAAGGGTGTGACTTAGGGGGGTATGAGTGATACAGAGGTATGGAAGG GAGTAGGTCAGAGGTGTGGAAGGGTGTGACTT_GGGGGGTATGAGTGATACAGAGGTATGGAAGG TA T SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43423757..43423903 26863196 MeRIP-seq:(Medium) rs1353109577 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23396202 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88588 RMVar_ID_88588 Human_SNP_ID_11236807 m1A Human chr1 + 43423923 43423882 43423923 GTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCAGGGTATCAGTGGTACAGAGATGTGGAAGGGCA _________________________________GGGTATCAGTGGTACAGAGATGTGGAAGGGCA GGGGTATGAGTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCA G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43423874..43424007 26863196 MeRIP-seq:(Medium) rs1557549758 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_258973,Human_RBP_ID_23396204 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88589 RMVar_ID_88589 Human_SNP_ID_11236830 m1A Human chr1 + 43423923 43423923 43423923 GTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCAGGGTATCAGTGGTACAGAGATGTGGAAGGGCA GTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCCGGGTATCAGTGGTACAGAGATGTGGAAGGGCA A C SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43423874..43424007 26863196 MeRIP-seq:(Medium) rs1459669232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258973,Human_RBP_ID_23396204 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88590 RMVar_ID_88590 Human_SNP_ID_11236831 m1A Human chr1 + 43423923 43423923 43423923 GTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCAGGGTATCAGTGGTACAGAGATGTGGAAGGGCA GTGGTAAGGAGTGTGGAAGGGTGTGGCTTAGCGGGGTATCAGTGGTACAGAGATGTGGAAGGGCA A G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43423874..43424007 26863196 MeRIP-seq:(Medium) rs1459669232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258973,Human_RBP_ID_23396204 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88591 RMVar_ID_88591 Human_SNP_ID_11236843 m1A Human chr1 + 43423965 43423965 43423965 TGGTACAGAGATGTGGAAGGGCATGGTTTAGCAGGGTATGAGTGGTACAGAGGCATGGAAGGGCG TGGTACAGAGATGTGGAAGGGCATGGTTTAGCGGGGTATGAGTGGTACAGAGGCATGGAAGGGCG A G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43423334..43424207 26863196 MeRIP-seq:(Medium) rs1464611316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5333162,Human_RBP_ID_23396205 RMVar_hsa_circ_77566,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_86538,RMVar_hsa_circ_132260,RMVar_hsa_circ_88607,RMVar_hsa_circ_124065,RMVar_hsa_circ_132262,RMVar_hsa_circ_115278,RMVar_hsa_circ_132263,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_106023,RMVar_hsa_circ_132265,RMVar_hsa_circ_90801,RMVar_hsa_circ_126307,RMVar_hsa_circ_132268,RMVar_hsa_circ_121878,RMVar_hsa_circ_132270,RMVar_hsa_circ_132271,RMVar_hsa_circ_51518,RMVar_hsa_circ_266034 88592 RMVar_ID_88592 Human_SNP_ID_11245419 m1A Human chr1 - 43451210 43451210 43451210 AGTGAGGGCCCGCACACCACCCACGTGCCTCCAGACAGCGAGTGACATCCCATCTCCTCCTCTGC AGTGAGGGCCCGCACACCACCCACGTGCCTCCGGACAGCGAGTGACATCCCATCTCCTCCTCTGC T C HYI Ensembl:ENSG00000178922 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43451151..43451225 26863196 MeRIP-seq:(Medium) rs113428386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1545248 88593 RMVar_ID_88593 Human_SNP_ID_11264781 m1A Human chr1 - 43530923 43530911 43530923 CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGAAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCG____________CCGCCTCTGCCGCCGCCACCG GCGGCTCCAGCTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43530876..43538315;chr1:43530842..43531123;chr1:43530826..43545125;chr1:43530876..43545068 26863196 MeRIP-seq:(Medium) rs959734130 Functional Loss DEL dbSNP153 33..44 33 - - - 88594 RMVar_ID_88594 Human_SNP_ID_11264786 m1A Human chr1 - 43530923 43530917 43530923 CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGAAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCG______GAGCCGCCGCCTCTGCCGCCGCCACCG CCAGCTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43530876..43538315;chr1:43530842..43531123;chr1:43530826..43545125;chr1:43530876..43545068 26863196 MeRIP-seq:(Medium) rs1457331654 Functional Loss DEL dbSNP153 33..38 33 - - - 88595 RMVar_ID_88595 Human_SNP_ID_11264793 m1A Human chr1 - 43530923 43530923 43530923 CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGAAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGGAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43530876..43538315;chr1:43530842..43531123;chr1:43530826..43545125;chr1:43530876..43545068 26863196 MeRIP-seq:(Medium) rs1239474344 Functional Loss SNV dbSNP153 33..33 33 - - - 88596 RMVar_ID_88596 Human_SNP_ID_11264845 m1A Human chr1 - 43530987 43530987 43530987 CGCCGCCGCCTCCACCTGGTCCCGCTCCCGCCACCGCCACCCGAGCTGGAGCCGGAGCCGGAGCC CGCCGCCGCCTCCACCTGGTCCCGCTCCCGCCGCCGCCACCCGAGCTGGAGCCGGAGCCGGAGCC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:43530887..43531025 26863410 MeRIP-seq:(Medium) rs1557647446 Functional Loss SNV dbSNP153 33..33 33 - - - 88597 RMVar_ID_88597 Human_SNP_ID_11273320 m1A Human chr1 + 43563530 43563530 43563530 AGGACAGAAGGAGCCCCAGGAACCGACTCTCCATGTTGGGAGGAGGTTCCTGAGAGACTGGAGGG AGGACAGAAGGAGCCCCAGGAACCGACTCTCCGTGTTGGGAGGAGGTTCCTGAGAGACTGGAGGG A G PTPRF Ensembl:ENSG00000142949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43563524..43563640 26863196 MeRIP-seq:(Medium) rs1328336729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132289,RMVar_hsa_circ_124473,RMVar_hsa_circ_303201,RMVar_hsa_circ_336177,RMVar_hsa_circ_107142,RMVar_hsa_circ_284358,RMVar_hsa_circ_132290,RMVar_hsa_circ_345418,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_97544,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_132291,RMVar_hsa_circ_80635,RMVar_hsa_circ_132294 88598 RMVar_ID_88598 Human_SNP_ID_11273422 m1A Human chr1 + 43563927 43563927 43563927 CAGGGCATGGCCCCTGGGTTCTTGTGGTGGGGAGGCCTCAACTGGGTTGAGTAGGGCGATGTGGG CAGGGCATGGCCCCTGGGTTCTTGTGGTGGGGGGGCCTCAACTGGGTTGAGTAGGGCGATGTGGG A G PTPRF Ensembl:ENSG00000142949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43563922..43564019 26863196 MeRIP-seq:(Medium) rs1250065694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330279,Human_RBP_ID_8052632,Human_RBP_ID_8167028 RMVar_hsa_circ_132289,RMVar_hsa_circ_124473,RMVar_hsa_circ_303201,RMVar_hsa_circ_336177,RMVar_hsa_circ_107142,RMVar_hsa_circ_284358,RMVar_hsa_circ_132290,RMVar_hsa_circ_345418,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_97544,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_132291,RMVar_hsa_circ_80635,RMVar_hsa_circ_132294 88599 RMVar_ID_88599 Human_SNP_ID_11274780 m1A Human chr1 - 43568721 43568721 43568721 AGCAAACCCACTCCCACTGTACATGGGCTCCCATATCAGCCCCGAGGGGCTGCAGGGCAAGGCTA AGCAAACCCACTCCCACTGTACATGGGCTCCCGTATCAGCCCCGAGGGGCTGCAGGGCAAGGCTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43568716..43568821 32194978 MeRIP-seq:(Medium) rs1162816434 Functional Loss SNV dbSNP153 33..33 33 - - - 88600 RMVar_ID_88600 Human_SNP_ID_11279799 m1A Human chr1 - 43587180 43587180 43587180 CTGTTTAACAAGCTCCTGCATGGCTCCCAGTGACTCCTCTGCCCAGCCCAAGAGACCCTACCTAA CTGTTTAACAAGCTCCTGCATGGCTCCCAGTGTCTCCTCTGCCCAGCCCAAGAGACCCTACCTAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43587174..43587328 26863196 MeRIP-seq:(Medium) rs1437419442 Functional Loss SNV dbSNP153 33..33 33 - - - 88601 RMVar_ID_88601 Human_SNP_ID_11283110 m1A Human chr1 - 43597802 43597802 43597802 TGTCGGCAGGCGGCGGGACCCAACTTACCCGGACCGTGGTGGAGCCCATGCTCACACACATCACC TGTCGGCAGGCGGCGGGACCCAACTTACCCGGGCCGTGGTGGAGCCCATGCTCACACACATCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43597751..43598075 32194978 MeRIP-seq:(Medium) rs1447541618 Functional Loss SNV dbSNP153 33..33 33 - - - 88602 RMVar_ID_88602 Human_SNP_ID_11283155 m1A Human chr1 + 43597892 43597892 43597892 CTCCGTGGCCTACGAGGCGGTGGACGGCGAGGACCGCGGGCGGCATGTGGTGGATGGCATCAGCC CTCCGTGGCCTACGAGGCGGTGGACGGCGAGGGCCGCGGGCGGCATGTGGTGGATGGCATCAGCC A G PTPRF Ensembl:ENSG00000142949 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43597841..43598028 26863196 MeRIP-seq:(Medium) rs1410767912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27399090 RMVar_hsa_circ_107142,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_80635,RMVar_hsa_circ_267194,RMVar_hsa_circ_79921,RMVar_hsa_circ_97671,RMVar_hsa_circ_132299,RMVar_hsa_circ_127388,RMVar_hsa_circ_132304,RMVar_hsa_circ_132305,RMVar_hsa_circ_115377,RMVar_hsa_circ_84667,RMVar_hsa_circ_81129,RMVar_hsa_circ_132306,RMVar_hsa_circ_132308,RMVar_hsa_circ_21186,RMVar_hsa_circ_66818,RMVar_hsa_circ_132309 88603 RMVar_ID_88603 Human_SNP_ID_11283384 m1A Human chr1 + 43598648 43598648 43598648 CTGGGGGAGTGGGGTGCTGAGGCAGGACCCTCAAGTTTGCTGTGCCCACCTGAGCTAGGGTTGAT CTGGGGGAGTGGGGTGCTGAGGCAGGACCCTCGAGTTTGCTGTGCCCACCTGAGCTAGGGTTGAT A G PTPRF Ensembl:ENSG00000142949 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17849103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22535198,Human_RBP_ID_22864424 GWAS_ID_11163,GWAS_ID_11164,GWAS_ID_11165,GWAS_ID_11166 RMVar_hsa_circ_107142,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_80635,RMVar_hsa_circ_267194,RMVar_hsa_circ_79921,RMVar_hsa_circ_97671,RMVar_hsa_circ_132299,RMVar_hsa_circ_127388,RMVar_hsa_circ_132304,RMVar_hsa_circ_132305,RMVar_hsa_circ_115377,RMVar_hsa_circ_84667,RMVar_hsa_circ_81129,RMVar_hsa_circ_132306,RMVar_hsa_circ_132308,RMVar_hsa_circ_21186,RMVar_hsa_circ_66818,RMVar_hsa_circ_132309 88604 RMVar_ID_88604 Human_SNP_ID_11283442 m1A Human chr1 + 43598819 43598819 43598819 GAAGCTGCCTGTCCCCAGCAAGCAGCATGGCCAGATCCGCGGCTACCAGGTCACCTACGTGCGGC GAAGCTGCCTGTCCCCAGCAAGCAGCATGGCCGGATCCGCGGCTACCAGGTCACCTACGTGCGGC A G PTPRF Ensembl:ENSG00000142949 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:43598731..43598915 26863196 MeRIP-seq:(Medium) rs1404378647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_58548,Human_Splice_Rec_58549,Human_Splice_Rec_58614,Human_Splice_Rec_58615,Human_Splice_Rec_58700,Human_Splice_Rec_58701,Human_Splice_Rec_58750,Human_Splice_Rec_58751,Human_Splice_Rec_58796,Human_Splice_Rec_58797,Human_Splice_Rec_58839,Human_Splice_Rec_58879 Human_miRNA_ID_2392085 RMVar_hsa_circ_107142,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_80635,RMVar_hsa_circ_267194,RMVar_hsa_circ_79921,RMVar_hsa_circ_97671,RMVar_hsa_circ_132299,RMVar_hsa_circ_127388,RMVar_hsa_circ_132304,RMVar_hsa_circ_132305,RMVar_hsa_circ_115377,RMVar_hsa_circ_84667,RMVar_hsa_circ_81129,RMVar_hsa_circ_132306,RMVar_hsa_circ_132308,RMVar_hsa_circ_21186,RMVar_hsa_circ_66818,RMVar_hsa_circ_132309 88605 RMVar_ID_88605 Human_SNP_ID_11283470 m1A Human chr1 + 43598881 43598881 43598881 GGCTGGAGAATGGCGAGCCCCGTGGACTCCCCATCATCCAAGACGTCATGCTAGCCGAGGCCCAG GGCTGGAGAATGGCGAGCCCCGTGGACTCCCCGTCATCCAAGACGTCATGCTAGCCGAGGCCCAG A G PTPRF Ensembl:ENSG00000142949 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43598701..43598925 32194978 MeRIP-seq:(Medium) rs373814583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_58549,Human_Splice_Rec_58615,Human_Splice_Rec_58701,Human_Splice_Rec_58751,Human_Splice_Rec_58797,Human_Splice_Rec_58839,Human_Splice_Rec_58879 RMVar_hsa_circ_107142,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_80635,RMVar_hsa_circ_267194,RMVar_hsa_circ_79921,RMVar_hsa_circ_97671,RMVar_hsa_circ_132299,RMVar_hsa_circ_127388,RMVar_hsa_circ_132304,RMVar_hsa_circ_132305,RMVar_hsa_circ_115377,RMVar_hsa_circ_84667,RMVar_hsa_circ_81129,RMVar_hsa_circ_132306,RMVar_hsa_circ_132308,RMVar_hsa_circ_21186,RMVar_hsa_circ_66818,RMVar_hsa_circ_132309 88606 RMVar_ID_88606 Human_SNP_ID_11284854 m1A Human chr1 - 43603846 43603842 43603846 CTGATCTCCTTCTCGAACTCCTCACCCAAGCCAGCCCGGTTCTTGGCAGCAAGCCGGAAGATGTA CTGATCTCCTTCTCGAACTCCTCACCCAAGCC____CGGTTCTTGGCAGCAAGCCGGAAGATGTA GGGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43603798..43604014 26863196 MeRIP-seq:(Medium) rs1270506202 Functional Loss DEL dbSNP153 33..36 33 - - - 88607 RMVar_ID_88607 Human_SNP_ID_11290473 m1A Human chr1 + 43621229 43621228 43621230 CTGCGTACACAGCGTCCTGCCATGGTGCAGACAGAGGTAACGCAGACCAGGCTGCAGGGCCAGGG CTGCGTACACAGCGTCCTGCCATGGTGCAGAC__AGGTAACGCAGACCAGGCTGCAGGGCCAGGG CAG C PTPRF Ensembl:ENSG00000142949 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43621076..43621250 32194978 MeRIP-seq:(Medium) rs1400141404 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_58589,Human_Splice_Rec_58653,Human_Splice_Rec_58741,Human_Splice_Rec_58789,Human_Splice_Rec_58837,Human_Splice_Rec_58877,Human_Splice_Rec_58919,Human_Splice_Rec_58943 RMVar_hsa_circ_267194,RMVar_hsa_circ_132316,RMVar_hsa_circ_372862,RMVar_hsa_circ_105228,RMVar_hsa_circ_132319,RMVar_hsa_circ_132320,RMVar_hsa_circ_94962 88608 RMVar_ID_88608 Human_SNP_ID_11290859 m1A Human chr1 - 43622427 43622427 43622427 AGAAAAAAAAAAACAAAACAAAATAAACCCCAACCCCTACAGTGGCCCATTCTGCAGATACGGAT AGAAAAAAAAAAACAAAACAAAATAAACCCCATCCCCTACAGTGGCCCATTCTGCAGATACGGAT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43622376..43622475 32194978 MeRIP-seq:(Medium) rs1389416053 Functional Loss SNV dbSNP153 33..33 33 - - - 88609 RMVar_ID_88609 Human_SNP_ID_11302219 m1A Human chr1 - 43664465 43664465 43664465 TCACTCACTTCTCATCGTTTTACACAGCACCCAAACTACAGCAGACTCCCCCTAGCTCCCTAAAC TCACTCACTTCTCATCGTTTTACACAGCACCCTAACTACAGCAGACTCCCCCTAGCTCCCTAAAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43664432..43664516 26863196 MeRIP-seq:(Medium) rs1557906305 Functional Loss SNV dbSNP153 33..33 33 - - - 88610 RMVar_ID_88610 Human_SNP_ID_11303020 m1A Human chr1 + 43667968 43667966 43667969 TCCAAGAGCTGGCAACGAGGAGGAGTGCCCAGAGGAGGACATGGAAGGGGTGGAGGATGGAGAGG TCCAAGAGCTGGCAACGAGGAGGAGTGCCCA___GAGGACATGGAAGGGGTGGAGGATGGAGAGG AGAG A KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43667917..43668057 26863196 MeRIP-seq:(Medium) rs756653660 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_221120,Human_RBP_ID_5518983,Human_RBP_ID_9356223,Human_RBP_ID_18965395,Human_RBP_ID_22870832,Human_RBP_ID_26314102 Human_Splice_Rec_58961 RMVar_hsa_circ_10387,RMVar_hsa_circ_11888,RMVar_hsa_circ_324177,RMVar_hsa_circ_355215,RMVar_hsa_circ_19285,RMVar_hsa_circ_10640,RMVar_hsa_circ_265841,RMVar_hsa_circ_96119,RMVar_hsa_circ_69339,RMVar_hsa_circ_132323,RMVar_hsa_circ_373060,RMVar_hsa_circ_35159,RMVar_hsa_circ_334631,RMVar_hsa_circ_132325,RMVar_hsa_circ_132326,RMVar_hsa_circ_132327,RMVar_hsa_circ_106359 88611 RMVar_ID_88611 Human_SNP_ID_11327422 m1A Human chr1 - 43767265 43767265 43767265 ATGCCATGCCTTGCACTCTTGCGCCTCTATCCATAATCTTCCCTCTGCCTTTCTGCTCCTCCTAG ATGCCATGCCTTGCACTCTTGCGCCTCTATCCGTAATCTTCCCTCTGCCTTTCTGCTCCTCCTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43767173..43767312 26863196 MeRIP-seq:(Medium) rs924414162 Functional Loss SNV dbSNP153 33..33 33 - - - 88612 RMVar_ID_88612 Human_SNP_ID_11350672 m1A Human chr1 + 43870702 43870702 43870702 CTGAATCTCAGGCCAGGACCTGTGGTTTGTGCATGTGAACTGTTCCCGGGAGAGCCTGTGATGGG CTGAATCTCAGGCCAGGACCTGTGGTTTGTGCGTGTGAACTGTTCCCGGGAGAGCCTGTGATGGG A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43870695..43870835 26863196 MeRIP-seq:(Medium) rs1489108190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5322,RMVar_hsa_circ_40460,RMVar_hsa_circ_8358,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_321076,RMVar_hsa_circ_375524,RMVar_hsa_circ_48260,RMVar_hsa_circ_7537,RMVar_hsa_circ_132340 88613 RMVar_ID_88613 Human_SNP_ID_11350849 m1A Human chr1 + 43871449 43871449 43871449 GGGAGAGGACGGGGTGTGAGGGAGAAGATGGCATGTGAAGAAGAGGATGGGGTGTGAGGGAGAGG GGGAGAGGACGGGGTGTGAGGGAGAAGATGGCTTGTGAAGAAGAGGATGGGGTGTGAGGGAGAGG A T AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43871241..43871482 26863196 MeRIP-seq:(Medium) rs1251916172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5322,RMVar_hsa_circ_40460,RMVar_hsa_circ_8358,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_321076,RMVar_hsa_circ_375524,RMVar_hsa_circ_48260,RMVar_hsa_circ_7537,RMVar_hsa_circ_132340 88614 RMVar_ID_88614 Human_SNP_ID_11351191 m1A Human chr1 + 43872323 43872323 43872323 GAGAGGGTGTGTTGGGGAGAGGTGAGAGGGGGAGTGTTGGGGAAGGGTGTGAGCGAGACGGGGTG GAGAGGGTGTGTTGGGGAGAGGTGAGAGGGGGGGTGTTGGGGAAGGGTGTGAGCGAGACGGGGTG A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43872286..43872472 26863196 MeRIP-seq:(Medium) rs1370825763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258492,Human_RBP_ID_3328381,Human_RBP_ID_5233929,Human_RBP_ID_8167041,Human_RBP_ID_9411869,Human_RBP_ID_22520275 RMVar_hsa_circ_5322,RMVar_hsa_circ_40460,RMVar_hsa_circ_8358,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_321076,RMVar_hsa_circ_375524,RMVar_hsa_circ_48260,RMVar_hsa_circ_7537,RMVar_hsa_circ_132340 88615 RMVar_ID_88615 Human_SNP_ID_11352639 m1A Human chr1 + 43878605 43878605 43878605 GCAGCAAGGAGTGTGGCTGGGGGACTGTGAACAGAGGGAGAGTAGTAGGAGATGAGACCAGAGAG GCAGCAAGGAGTGTGGCTGGGGGACTGTGAACGGAGGGAGAGTAGTAGGAGATGAGACCAGAGAG A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43878547..43878637 26863196 MeRIP-seq:(Medium) rs1166432584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5322,RMVar_hsa_circ_40460,RMVar_hsa_circ_8358,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_321076,RMVar_hsa_circ_375524,RMVar_hsa_circ_48260,RMVar_hsa_circ_7537,RMVar_hsa_circ_132340 88616 RMVar_ID_88616 Human_SNP_ID_11358500 m1A Human chr1 - 43904761 43904761 43904761 GGAGGAAGAGTGGCAGGAAGAGGAGCAGGAGGAGGGGAGAGTGGTGGGAAGAGGAGCAGGAGGGG GGAGGAAGAGTGGCAGGAAGAGGAGCAGGAGGTGGGGAGAGTGGTGGGAAGAGGAGCAGGAGGGG T A HSALNG0003123 RNACentral:URS0000E9E5D6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43904725..43904790 26863196 MeRIP-seq:(Medium) rs1239774271 Functional Loss SNV dbSNP153 33..33 33 - - - 88617 RMVar_ID_88617 Human_SNP_ID_11358501 m1A Human chr1 - 43904761 43904761 43904761 GGAGGAAGAGTGGCAGGAAGAGGAGCAGGAGGAGGGGAGAGTGGTGGGAAGAGGAGCAGGAGGGG GGAGGAAGAGTGGCAGGAAGAGGAGCAGGAGGGGGGGAGAGTGGTGGGAAGAGGAGCAGGAGGGG T C HSALNG0003123 RNACentral:URS0000E9E5D6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43904725..43904790 26863196 MeRIP-seq:(Medium) rs1239774271 Functional Loss SNV dbSNP153 33..33 33 - - - 88618 RMVar_ID_88618 Human_SNP_ID_11358547 m1A Human chr1 - 43904839 43904837 43904840 GGAGGAGGAGGAGGAAGAGTGGCAGGAATAGGAGCAGGAGGAGGGGAAAGAGTGGCAGGAAGAGG GGAGGAGGAGGAGGAAGAGTGGCAGGAATAG___CAGGAGGAGGGGAAAGAGTGGCAGGAAGAGG GCTC G HSALNG0003123 RNACentral:URS0000E9E5D6 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43904788..43904898 26863196 MeRIP-seq:(Medium) rs1395494299 Functional Loss DEL dbSNP153 32..34 33 - - - 88619 RMVar_ID_88619 Human_SNP_ID_11358549 m1A Human chr1 - 43904839 43904839 43904839 GGAGGAGGAGGAGGAAGAGTGGCAGGAATAGGAGCAGGAGGAGGGGAAAGAGTGGCAGGAAGAGG GGAGGAGGAGGAGGAAGAGTGGCAGGAATAGGGGCAGGAGGAGGGGAAAGAGTGGCAGGAAGAGG T C HSALNG0003123 RNACentral:URS0000E9E5D6 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43904788..43904898 26863196 MeRIP-seq:(Medium) rs1328934168 Functional Loss SNV dbSNP153 33..33 33 - - - 88620 RMVar_ID_88620 Human_SNP_ID_11358587 m1A Human chr1 - 43904893 43904893 43904893 GTGGCGGGAAGAGGAGCAGGAGGAGGGGGAGGAAGAGTGGCGGGAAGAGGAGCAGGAGGAGGAGG GTGGCGGGAAGAGGAGCAGGAGGAGGGGGAGGGAGAGTGGCGGGAAGAGGAGCAGGAGGAGGAGG T C HSALNG0003123 RNACentral:URS0000E9E5D6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43904854..43904919 26863196 MeRIP-seq:(Medium) rs774401314 Functional Loss SNV dbSNP153 33..33 33 - - - 88621 RMVar_ID_88621 Human_SNP_ID_11361827 m1A Human chr1 - 43915641 43915641 43915641 TGATGCTGCTCCTTGTCTCTAACATCCTTCCCACCTCTATCCACATGACCCATCCATTTTCTAAG TGATGCTGCTCCTTGTCTCTAACATCCTTCCCGCCTCTATCCACATGACCCATCCATTTTCTAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43915590..43915785 26863196 MeRIP-seq:(Medium) rs1028069823 Functional Loss SNV dbSNP153 33..33 33 - - - 88622 RMVar_ID_88622 Human_SNP_ID_11361828 m1A Human chr1 + 43915661 43915661 43915661 TGTGGATAGAGGTGGGAAGGATGTTAGAGACAAGGAGCAGCATCAGCAAAAGTGTGGGGCATGAA TGTGGATAGAGGTGGGAAGGATGTTAGAGACAGGGAGCAGCATCAGCAAAAGTGTGGGGCATGAA A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43915581..43915734 26863196 MeRIP-seq:(Medium) rs968425291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23396884 RMVar_hsa_circ_40460,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_375524,RMVar_hsa_circ_132340,RMVar_hsa_circ_6171,RMVar_hsa_circ_310045,RMVar_hsa_circ_132343,RMVar_hsa_circ_289601 88623 RMVar_ID_88623 Human_SNP_ID_11368302 m1A Human chr1 + 43939635 43939634 43939635 TCTTGGTCCAATACTCTCCGGGTTCTCCTTCCACTCCTCCAGAGGCTTGTTCTCAGACGACTTCT TCTTGGTCCAATACTCTCCGGGTTCTCCTTCC_CTCCTCCAGAGGCTTGTTCTCAGACGACTTCT CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43939584..43940201 26863196 MeRIP-seq:(Medium) rs1264417712 Functional Loss DEL dbSNP153 33..33 33 - - - 88624 RMVar_ID_88624 Human_SNP_ID_11368308 m1A Human chr1 + 43939662 43939662 43939662 CTTCCACTCCTCCAGAGGCTTGTTCTCAGACGACTTCTGAGTTCCTCTTCCTCTCTCTGCCTCTC CTTCCACTCCTCCAGAGGCTTGTTCTCAGACGGCTTCTGAGTTCCTCTTCCTCTCTCTGCCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43939611..43940277 26863196 MeRIP-seq:(Medium) rs1265481226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2148894 88625 RMVar_ID_88625 Human_SNP_ID_11374141 m1A Human chr1 + 43965574 43965574 43965574 TGGATGGGTATGTTGGAAGAGTGCACAGGGGGACTGTGGGAAGGCTGAGGGTGTAGGTGTGTGGA TGGATGGGTATGTTGGAAGAGTGCACAGGGGGCCTGTGGGAAGGCTGAGGGTGTAGGTGTGTGGA A C IPO13 Ensembl:ENSG00000117408 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43965450..43965852 26863196 MeRIP-seq:(Medium) rs762827956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5641660 88626 RMVar_ID_88626 Human_SNP_ID_11376931 m1A Human chr1 - 43975099 43975099 43975099 CCGCCCGCCAGGACCCGGCCTCACCCACGGCCAGCGCGCAGGCCCAGAAGGCCACGAAGACCCCG CCGCCCGCCAGGACCCGGCCTCACCCACGGCCTGCGCGCAGGCCCAGAAGGCCACGAAGACCCCG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:43974976..43975178 26863196 MeRIP-seq:(Medium) rs1272528020 Functional Loss SNV dbSNP153 33..33 33 - - - 88627 RMVar_ID_88627 Human_SNP_ID_11377072 m1A Human chr1 + 43975469 43975469 43975469 TTCCTCTTTTCCCAGTCGCTTTGCCCTCCCCCACCCACAGCTTGTTGGGTAAACAGCGGAACGGA TTCCTCTTTTCCCAGTCGCTTTGCCCTCCCCCCCCCACAGCTTGTTGGGTAAACAGCGGAACGGA A C ATP6V0B Ensembl:ENSG00000117410 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43975465..43975565 32194978 MeRIP-seq:(Medium) rs1173607535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18928322,Human_RBP_ID_23396970 RMVar_hsa_circ_84651,RMVar_hsa_circ_132359 88628 RMVar_ID_88628 Human_SNP_ID_11378275 m1A Human chr1 - 43979322 43979322 43979322 CGCCGCCGCCGCCGCCGCGGGCCATGGAGCCGAGCCGCCCCGGGGGGCAGGGCGGGGCCGGGCGG CGCCGCCGCCGCCGCCGCGGGCCATGGAGCCGGGCCGCCCCGGGGGGCAGGGCGGGGCCGGGCGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:43979233..43979525 26863410 MeRIP-seq:(Medium) rs1343019488 Functional Loss SNV dbSNP153 33..33 33 - - - 88629 RMVar_ID_88629 Human_SNP_ID_11378300 m1A Human chr1 + 43979366 43979366 43979366 CCCGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGGCGACCCGGGGGCCGCGGTGGCCGCTGACCG CCCGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGGCGACCCGGGGGCCGCGGTGGCCGCTGACCG A G B4GALT2 Ensembl:ENSG00000117411 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:43979201..43979617;chr1:43979226..43979450 26863196 MeRIP-seq:(Medium) rs953048987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072778,Human_RBP_ID_9318896 RMVar_hsa_circ_118377,RMVar_hsa_circ_132366 88630 RMVar_ID_88630 Human_SNP_ID_11378465 m1A Human chr1 + 43979973 43979973 43979973 CCCTGCGCCGGAGGGAGGGTGGGAATGTCTGCACGTGGGTCTGGGTGTGAGCTGTCTGAGAGTCT CCCTGCGCCGGAGGGAGGGTGGGAATGTCTGCTCGTGGGTCTGGGTGTGAGCTGTCTGAGAGTCT A T B4GALT2 Ensembl:ENSG00000117411 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:43979968..43980202 26863196 MeRIP-seq:(Medium) rs1457871890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4054800,Human_RBP_ID_23255531,Human_RBP_ID_23397020 Human_Splice_Rec_60815,Human_Splice_Rec_60827 RMVar_hsa_circ_118377,RMVar_hsa_circ_132366 88631 RMVar_ID_88631 Human_SNP_ID_11378660 m1A Human chr1 - 43980842 43980842 43980842 TACCTTCCTCCACCTCACTGACACACACACTCAGGCACTCACCCTTATTGCACAACTCTACACAC TACCTTCCTCCACCTCACTGACACACACACTCGGGCACTCACCCTTATTGCACAACTCTACACAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43980832..43980989 26863196 MeRIP-seq:(Medium) rs1475896534 Functional Loss SNV dbSNP153 33..33 33 - - - 88632 RMVar_ID_88632 Human_SNP_ID_11378835 m1A Human chr1 + 43981324 43981324 43981324 CTTCAGTGCCCGAGGCCCTGCCCATGCCCTCCACCCAGCTGCTAGCAGCAGCAGCAGCAGCAGCA CTTCAGTGCCCGAGGCCCTGCCCATGCCCTCCGCCCAGCTGCTAGCAGCAGCAGCAGCAGCAGCA A G B4GALT2 Ensembl:ENSG00000117411 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43981276..43981717 26863196 MeRIP-seq:(Medium) rs779365326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803165,Human_RBP_ID_4072781,Human_RBP_ID_22488256 Human_miRNA_ID_2648910,Human_miRNA_ID_2650857 RMVar_hsa_circ_118377,RMVar_hsa_circ_96896,RMVar_hsa_circ_132366,RMVar_hsa_circ_132367,RMVar_hsa_circ_268936 88633 RMVar_ID_88633 Human_SNP_ID_11378902 m1A Human chr1 - 43981441 43981441 43981441 CAAGACCAGGTGGCGAGTCAGGACAGGGTGGCAGCGTGGGAGCCGTGGGACCGGGCAGGGCACTG CAAGACCAGGTGGCGAGTCAGGACAGGGTGGCGGCGTGGGAGCCGTGGGACCGGGCAGGGCACTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:43981343..43981475 26863196 MeRIP-seq:(Medium) rs375270042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86054,RMVar_hsa_circ_132368 88634 RMVar_ID_88634 Human_SNP_ID_11379032 m1A Human chr1 - 43981853 43981853 43981853 CCTCAAGATGGGGTGTAGATAGTGGAGCCAGTAGCGCAGGTGGTGTTCCCGGTGTCTAAAGGGGA CCTCAAGATGGGGTGTAGATAGTGGAGCCAGTGGCGCAGGTGGTGTTCCCGGTGTCTAAAGGGGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:43981701..43981925 26863196 MeRIP-seq:(Medium) rs774875002 Functional Loss SNV dbSNP153 33..33 33 - - - 88635 RMVar_ID_88635 Human_SNP_ID_11379822 m1A Human chr1 + 43984915 43984915 43984915 AACCGGGCCAAGCTGCTTAACGTGGGCTTCCTAGAGGCGCTGAAGGAGGATGCCGCCTATGACTG AACCGGGCCAAGCTGCTTAACGTGGGCTTCCTGGAGGCGCTGAAGGAGGATGCCGCCTATGACTG A G B4GALT2 Ensembl:ENSG00000117411 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43984845..43984997 26863196 MeRIP-seq:(Medium) rs1285609456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356054,Human_RBP_ID_3314032,Human_RBP_ID_5828569,Human_RBP_ID_8312159,Human_RBP_ID_8749703,Human_RBP_ID_17218759,Human_RBP_ID_23397064 Human_Splice_Rec_60780,Human_Splice_Rec_60796,Human_Splice_Rec_60808,Human_Splice_Rec_60820,Human_Splice_Rec_60832 RMVar_hsa_circ_118377,RMVar_hsa_circ_96896,RMVar_hsa_circ_132366,RMVar_hsa_circ_132367,RMVar_hsa_circ_22590,RMVar_hsa_circ_34615 88636 RMVar_ID_88636 Human_SNP_ID_11379970 m1A Human chr1 - 43985374 43985374 43985374 ACTCACCGGTTGAAGATGTCATCATCCTCGCCACCCCAGCCCCAGTACTCATTGGGGAAGCCATT ACTCACCGGTTGAAGATGTCATCATCCTCGCCCCCCCAGCCCCAGTACTCATTGGGGAAGCCATT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43985325..43985422 26863196 MeRIP-seq:(Medium) rs144638219 Functional Loss SNV dbSNP153 33..33 33 - - - 88637 RMVar_ID_88637 Human_SNP_ID_11381467 m1A Human chr1 + 43990538 43990538 43990538 CCTGGCTGGCAGCTGCTCTGTGGAGGACCTCCAGGACTGAGACTGGGCTCTGTTTTCCAAGGGTC CCTGGCTGGCAGCTGCTCTGTGGAGGACCTCCCGGACTGAGACTGGGCTCTGTTTTCCAAGGGTC A C B4GALT2 Ensembl:ENSG00000117411 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43990276..43990624 32194978 MeRIP-seq:(Medium) rs1408639630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356081,Human_RBP_ID_18575791,Human_RBP_ID_23397069,Human_RBP_ID_27183840,Human_RBP_ID_27399214 88638 RMVar_ID_88638 Human_SNP_ID_11381514 m1A Human chr1 - 43990673 43990673 43990673 GGGGCTGGGCTAGGGGGAGGGGGTCGGGAAGGAGGGTTGACTCCAAAGAGGGCCACACTTGAAGA GGGGCTGGGCTAGGGGGAGGGGGTCGGGAAGGCGGGTTGACTCCAAAGAGGGCCACACTTGAAGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43990624..43990796 26863196 MeRIP-seq:(Medium) rs1239084863 Functional Loss SNV dbSNP153 33..33 33 - - - 88639 RMVar_ID_88639 Human_SNP_ID_11381995 m1A Human chr1 + 43991852 43991852 43991852 TCCCGCACTCTGACCTGCGGCCCGTAGGTCCGAGCCGGGGACGGCGGCGTCGGTGGGTCATGCTC TCCCGCACTCTGACCTGCGGCCCGTAGGTCCGGGCCGGGGACGGCGGCGTCGGTGGGTCATGCTC A G CCDC24 Ensembl:ENSG00000159214 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43991802..43991942 26863196 MeRIP-seq:(Medium) rs1210728701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_60840,Human_Splice_Rec_60854,Human_Splice_Rec_60870,Human_Splice_Rec_60880,Human_Splice_Rec_60890 88640 RMVar_ID_88640 Human_SNP_ID_11382007 m1A Human chr1 - 43991873 43991873 43991873 CCACAGCGAGGGGGAGTGCCGGAGCATGACCCACCGACGCCGCCGTCCCCGGCTCGGACCTACGG CCACAGCGAGGGGGAGTGCCGGAGCATGACCCGCCGACGCCGCCGTCCCCGGCTCGGACCTACGG T C SLC6A9 Ensembl:ENSG00000196517 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43991822..43991946 26863196 MeRIP-seq:(Medium) rs775416891 Functional Loss SNV dbSNP153 33..33 33 - - - 88641 RMVar_ID_88641 Human_SNP_ID_11382180 m1A Human chr1 + 43992240 43992240 43992240 GCAGGTGGCGATGTTACGGGCACTGCTCCAAGAGGCTCGATCCTCTCAAGCCCCCAGCTCCCGCC GCAGGTGGCGATGTTACGGGCACTGCTCCAAGGGGCTCGATCCTCTCAAGCCCCCAGCTCCCGCC A G CCDC24 Ensembl:ENSG00000159214 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43992189..43992280 26863196 MeRIP-seq:(Medium) rs201854412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_60842,Human_Splice_Rec_60856,Human_Splice_Rec_60872 88642 RMVar_ID_88642 Human_SNP_ID_11383611 m1A Human chr1 + 43996631 43996628 43996632 GCCGGGGCTGTCACTGCACAGAGGACGGACAAATGAACACTTCAGGGATTCAGACACTTCAGAAG GCCGGGGCTGTCACTGCACAGAGGACGGAC____GAACACTTCAGGGATTCAGACACTTCAGAAG CAAAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43996580..43996786 26863196 MeRIP-seq:(Medium) rs1350554176 Functional Loss DEL dbSNP153 31..34 33 - - - 88643 RMVar_ID_88643 Human_SNP_ID_11384170 m1A Human chr1 + 43998240 43998240 43998240 GCGGTGAGTGGGAAGGCTCTGCGGAAGGGAGAAGTCTGTCTTTGCCACAGTCCTGAACTGGCCAA GCGGTGAGTGGGAAGGCTCTGCGGAAGGGAGACGTCTGTCTTTGCCACAGTCCTGAACTGGCCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43998230..43998566 26863196 MeRIP-seq:(Medium) rs955843304 Functional Loss SNV dbSNP153 33..33 33 - - - 88644 RMVar_ID_88644 Human_SNP_ID_11384171 m1A Human chr1 + 43998240 43998240 43998240 GCGGTGAGTGGGAAGGCTCTGCGGAAGGGAGAAGTCTGTCTTTGCCACAGTCCTGAACTGGCCAA GCGGTGAGTGGGAAGGCTCTGCGGAAGGGAGAGGTCTGTCTTTGCCACAGTCCTGAACTGGCCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:43998230..43998566 26863196 MeRIP-seq:(Medium) rs955843304 Functional Loss SNV dbSNP153 33..33 33 - - - 88645 RMVar_ID_88645 Human_SNP_ID_11386571 m1A Human chr1 + 44007011 44007011 44007011 CCCTTAGCCTGGCATGGGAGGCCCTGTGTTATATGATGCCTGCTGGCCTCTTCTGTCTTGTCACT CCCTTAGCCTGGCATGGGAGGCCCTGTGTTATGTGATGCCTGCTGGCCTCTTCTGTCTTGTCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44007007..44007207 26863196 MeRIP-seq:(Medium) rs1402392048 Functional Loss SNV dbSNP153 33..33 33 - - - 88646 RMVar_ID_88646 Human_SNP_ID_11386949 m1A Human chr1 - 44008443 44008443 44008443 CGCCGGTGTACTGGACGCCTCCAACCTCACCAATGGCTCTCGGCCAGCCGCCTTGCCCAGCAACC CGCCGGTGTACTGGACGCCTCCAACCTCACCAGTGGCTCTCGGCCAGCCGCCTTGCCCAGCAACC T C SLC6A9 Ensembl:ENSG00000196517 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44008392..44008516 26863196 MeRIP-seq:(Medium) rs760214835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1348742,Human_RBP_ID_9356228,Human_RBP_ID_17752149 Human_Splice_Rec_60961,Human_Splice_Rec_60983,Human_Splice_Rec_61003,Human_Splice_Rec_61027,Human_Splice_Rec_61047,Human_Splice_Rec_61071,Human_Splice_Rec_61093 RMVar_hsa_circ_11885,RMVar_hsa_circ_19298,RMVar_hsa_circ_132373,RMVar_hsa_circ_271801,RMVar_hsa_circ_373963,RMVar_hsa_circ_132374 88647 RMVar_ID_88647 Human_SNP_ID_11391171 m1A Human chr1 - 44024325 44024325 44024325 GAGATCTGTGGCCTGAAAGGCGCTGGAAGCAGAGCCTGTGAGTGTGGTCCCCGTCACCAGAGCCC GAGATCTGTGGCCTGAAAGGCGCTGGAAGCAGGGCCTGTGAGTGTGGTCCCCGTCACCAGAGCCC T C SLC6A9 Ensembl:ENSG00000196517 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:44024276..44024325 26863196 MeRIP-seq:(Medium) rs754560623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075534,Human_RBP_ID_18575828,Human_RBP_ID_23397103 Human_Splice_Rec_60976,Human_Splice_Rec_60977,Human_Splice_Rec_60996,Human_Splice_Rec_60997,Human_Splice_Rec_61020,Human_Splice_Rec_61021,Human_Splice_Rec_61044,Human_Splice_Rec_61045,Human_Splice_Rec_61110,Human_Splice_Rec_61111,Human_Splice_Rec_61126,Human_Splice_Rec_61127,Human_Splice_Rec_61130,Human_Splice_Rec_61131 88648 RMVar_ID_88648 Human_SNP_ID_11392355 m1A Human chr1 + 44029433 44029433 44029433 CGGCCATCTGCCGCCACGTGAGACTACCCAGCACTTGCAGAGGGCTCCTGCTTCATGCCTTTGCC CGGCCATCTGCCGCCACGTGAGACTACCCAGCGCTTGCAGAGGGCTCCTGCTTCATGCCTTTGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44029429..44029651 26863196 MeRIP-seq:(Medium) rs1427746553 Functional Loss SNV dbSNP153 33..33 33 - - - 88649 RMVar_ID_88649 Human_SNP_ID_11392708 m1A Human chr1 - 44030470 44030470 44030470 CCTGGAGAGCCCACCCCCGGCCGGCGCTCCGCACCCGGCAGCCACTGCAGATCTCGAGCAGGCGG CCTGGAGAGCCCACCCCCGGCCGGCGCTCCGCGCCCGGCAGCCACTGCAGATCTCGAGCAGGCGG T C SLC6A9 Ensembl:ENSG00000196517 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44030462..44030546 26863196 MeRIP-seq:(Medium) rs1216494033 Functional Loss SNV dbSNP153 33..33 33 - - - 88650 RMVar_ID_88650 Human_SNP_ID_11397569 m1A Human chr1 + 44051098 44051098 44051098 CGACAGCATGAGAGACGGAGAAAGAAATGGCCAGTTGGCAAGGTGGTAATGAGAGACAGCAGTTG CGACAGCATGAGAGACGGAGAAAGAAATGGCCGGTTGGCAAGGTGGTAATGAGAGACAGCAGTTG A G AL139220.2 Ensembl:ENSG00000230615 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:44051061..44051254;chr1:44051013..44051293;chr1:44051038..44051209;chr1:44051059..44051205 26863196 MeRIP-seq:(Medium) rs201175989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_61205 88651 RMVar_ID_88651 Human_SNP_ID_11413354 m1A Human chr1 + 44113546 44113546 44113546 ACCTAGGCCAGCCTGGGTATCAGGGAAGGCATAAGACAGGTAGGAGTTGGGTGGGGGAAGCATTA ACCTAGGCCAGCCTGGGTATCAGGGAAGGCATGAGACAGGTAGGAGTTGGGTGGGGGAAGCATTA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44113498..44113596 26863196 MeRIP-seq:(Medium) rs1232866430 Functional Loss SNV dbSNP153 33..33 33 - - - 88652 RMVar_ID_88652 Human_SNP_ID_11413355 m1A Human chr1 - 44113560 44113560 44113560 TTCCCACTCGTCACTAATGCTTCCCCCACCCAACTCCTACCTGTCTTATGCCTTCCCTGATACCC TTCCCACTCGTCACTAATGCTTCCCCCACCCAGCTCCTACCTGTCTTATGCCTTCCCTGATACCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:44113510..44113615 26863196 MeRIP-seq:(Medium) rs974032544 Functional Loss SNV dbSNP153 33..33 33 - - - 88653 RMVar_ID_88653 Human_SNP_ID_11437427 m1A Human chr1 + 44213740 44213740 44213740 GGCACTGACCCTTGACCTCCGGTGGCTCCCCCATCTCTCAGGCGCGATGGCTACGGGCGCGGATG GGCACTGACCCTTGACCTCCGGTGGCTCCCCCCTCTCTCAGGCGCGATGGCTACGGGCGCGGATG A C DMAP1 Ensembl:ENSG00000178028 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44213717..44213803 26863196 MeRIP-seq:(Medium) rs921702625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224611,Human_RBP_ID_4073973,Human_RBP_ID_18415528 Human_Splice_Rec_61284,Human_Splice_Rec_61318,Human_Splice_Rec_61324,Human_Splice_Rec_61336,Human_Splice_Rec_61342,Human_Splice_Rec_61348,Human_Splice_Rec_61356,Human_Splice_Rec_61374 88654 RMVar_ID_88654 Human_SNP_ID_11438453 m1A Human chr1 - 44217327 44217327 44217327 AATAGCCTCGCTACTGATCTCTGCCCACATTCAATCCGCTTCCAATCAATTCTCCATCTGCAGCT AATAGCCTCGCTACTGATCTCTGCCCACATTCTATCCGCTTCCAATCAATTCTCCATCTGCAGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44217282..44217572 26863196 MeRIP-seq:(Medium) rs1281712331 Functional Loss SNV dbSNP153 33..33 33 - - - 88655 RMVar_ID_88655 Human_SNP_ID_11438470 m1A Human chr1 + 44217420 44217420 44217420 AGGCCGACGGAGAAGTGGCAATGGAGACAGAAATTTTGGAGGTAAAAGCCACAGATTTGGTGAAG AGGCCGACGGAGAAGTGGCAATGGAGACAGAAGTTTTGGAGGTAAAAGCCACAGATTTGGTGAAG A G DMAP1 Ensembl:ENSG00000178028 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44217252..44217612 26863196 MeRIP-seq:(Medium) rs1415833408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1348748,Human_RBP_ID_11000024 88656 RMVar_ID_88656 Human_SNP_ID_11440381 m1A Human chr1 - 44224089 44224087 44224089 GTAAGTTCATACTTGATTAGATTTGGAGAGTGAGGGAGAGGGCAAAGTGGCAACATGACTCAGAT GTAAGTTCATACTTGATTAGATTTGGAGAGTG__GGAGAGGGCAAAGTGGCAACATGACTCAGAT CCT C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44224086..44224203 26863196 MeRIP-seq:(Medium) rs1471980369 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5828885 88657 RMVar_ID_88657 Human_SNP_ID_11440383 m1A Human chr1 - 44224089 44224089 44224089 GTAAGTTCATACTTGATTAGATTTGGAGAGTGAGGGAGAGGGCAAAGTGGCAACATGACTCAGAT GTAAGTTCATACTTGATTAGATTTGGAGAGTGGGGGAGAGGGCAAAGTGGCAACATGACTCAGAT T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44224086..44224203 26863196 MeRIP-seq:(Medium) rs1184397382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5828885 88658 RMVar_ID_88658 Human_SNP_ID_11440936 m1A Human chr1 + 44226748 44226745 44226748 TTGTCAGGCATTTCTTTATGGTTTCTAGGCTAATGTCTTGCTTCTCTATCTCAGCATTATTAAAC TTGTCAGGCATTTCTTTATGGTTTCTAGGC___TGTCTTGCTTCTCTATCTCAGCATTATTAAAC CTAA C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:44226717..44226803 26863410 MeRIP-seq:(Medium) rs1007763725 Functional Loss DEL dbSNP153 31..33 33 - - - 88659 RMVar_ID_88659 Human_SNP_ID_11441259 m1A Human chr1 + 44228087 44228087 44228087 CAGACATGGCCTACACAGTCCCCTGCGCCCCCATTCACGGCCACCTTGGCCCACCCGACCCACTT CAGACATGGCCTACACAGTCCCCTGCGCCCCCCTTCACGGCCACCTTGGCCCACCCGACCCACTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:44228080..44228191 26863196 MeRIP-seq:(Medium) rs1231387142 Functional Loss SNV dbSNP153 33..33 33 - - - 88660 RMVar_ID_88660 Human_SNP_ID_11443428 m1A Human chr1 + 44237875 44237857 44237875 GCCACGGTCTGCATGCCCACGTGCCTGATCCCACCCACGTGCCTGGCCTTGGCTCCCGGCGGCCG GCCACGGTCTGCATG__________________CCCACGTGCCTGGCCTTGGCTCCCGGCGGCCG GCCCACGTGCCTGATCCCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44237873..44237972 26863196 MeRIP-seq:(Medium) rs1049229622 Functional Loss DEL dbSNP153 16..33 33 - - - 88661 RMVar_ID_88661 Human_SNP_ID_11445036 m1A Human chr1 + 44244568 44244567 44244569 GTAGGTCCAAGGTAGTGTGTACTGAATGAAAGAAAGTTTTACCTGGTGTCCTACCTCTATTTCCA GTAGGTCCAAGGTAGTGTGTACTGAATGAAAG__AGTTTTACCTGGTGTCCTACCTCTATTTCCA GAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44244566..44245000 26863196 MeRIP-seq:(Medium) rs927710208 Functional Loss DEL dbSNP153 33..34 33 - - - 88662 RMVar_ID_88662 Human_SNP_ID_11445038 m1A Human chr1 + 44244568 44244568 44244568 GTAGGTCCAAGGTAGTGTGTACTGAATGAAAGAAAGTTTTACCTGGTGTCCTACCTCTATTTCCA GTAGGTCCAAGGTAGTGTGTACTGAATGAAAGGAAGTTTTACCTGGTGTCCTACCTCTATTTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44244566..44245000 26863196 MeRIP-seq:(Medium) rs1158995617 Functional Loss SNV dbSNP153 33..33 33 - - - 88663 RMVar_ID_88663 Human_SNP_ID_11445346 m1A Human chr1 + 44245884 44245881 44245885 CCCAGCCAGTTCTTCCTTCCCTGGACCAATGCAAGTCTTCTCACTGGTCCTCTTTGGTTCCTCCC CCCAGCCAGTTCTTCCTTCCCTGGACCAAT____GTCTTCTCACTGGTCCTCTTTGGTTCCTCCC TGCAA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44245880..44246030 26863196 MeRIP-seq:(Medium) rs986484521 Functional Loss DEL dbSNP153 31..34 33 - - - 88664 RMVar_ID_88664 Human_SNP_ID_11447252 m1A Human chr1 + 44254220 44254220 44254220 CTCTCAATTTCTTGACTCCCTGTGCTCTAATGAGCTTCTCCTCTACCTATTTCAGTCATCTTTCC CTCTCAATTTCTTGACTCCCTGTGCTCTAATGCGCTTCTCCTCTACCTATTTCAGTCATCTTTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44254218..44254560 26863196 MeRIP-seq:(Medium) rs889534189 Functional Loss SNV dbSNP153 33..33 33 - - - 88665 RMVar_ID_88665 Human_SNP_ID_11447478 m1A Human chr1 - 44255362 44255362 44255362 GCTAGGAAAACTGAGTAGAGTGTCAAGAAGGGAGAAGGGTTTCAGAGATGGAGCAGGCTGCAAAA GCTAGGAAAACTGAGTAGAGTGTCAAGAAGGGGGAAGGGTTTCAGAGATGGAGCAGGCTGCAAAA T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:44255348..44255479;chr1:44255261..44255390 26863196 MeRIP-seq:(Medium) rs1425041471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100254,RMVar_hsa_circ_132377,RMVar_hsa_circ_286708,RMVar_hsa_circ_292598,RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_24981,RMVar_hsa_circ_132380,RMVar_hsa_circ_132379 88666 RMVar_ID_88666 Human_SNP_ID_11452283 m1A Human chr1 - 44276468 44276468 44276468 TGAATAAGGAATCAAAAAACAGAAAGGATGGAAGAGACCTCCATAAGGATGTATGTGTATGTATG TGAATAAGGAATCAAAAAACAGAAAGGATGGAGGAGACCTCCATAAGGATGTATGTGTATGTATG T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44276456..44276782 26863196 MeRIP-seq:(Medium) rs553589613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100254,RMVar_hsa_circ_132377,RMVar_hsa_circ_286708,RMVar_hsa_circ_292598,RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_24981,RMVar_hsa_circ_132380,RMVar_hsa_circ_132379 88667 RMVar_ID_88667 Human_SNP_ID_11452291 m1A Human chr1 - 44276514 44276514 44276514 GCCATGGAAGTGGGTAGCTGATGTTGTATGGAAAAGAATGTTATTATGAATAAGGAATCAAAAAA GCCATGGAAGTGGGTAGCTGATGTTGTATGGAGAAGAATGTTATTATGAATAAGGAATCAAAAAA T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44276508..44276760 26863196 MeRIP-seq:(Medium) rs1208526726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23397331 RMVar_hsa_circ_100254,RMVar_hsa_circ_132377,RMVar_hsa_circ_286708,RMVar_hsa_circ_292598,RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_24981,RMVar_hsa_circ_132380,RMVar_hsa_circ_132379 88668 RMVar_ID_88668 Human_SNP_ID_11453898 m1A Human chr1 - 44283799 44283797 44283799 TTGGTGTGTGTGGGGGCTGGAGCTAAGCAAACATGTGGAGGAGCAGTGGAAGAGAAAGCTTTATA TTGGTGTGTGTGGGGGCTGGAGCTAAGCAAAC__GTGGAGGAGCAGTGGAAGAGAAAGCTTTATA CAT C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44283797..44283980 26863196 MeRIP-seq:(Medium) rs756207833 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5829206 RMVar_hsa_circ_100254,RMVar_hsa_circ_132377,RMVar_hsa_circ_286708,RMVar_hsa_circ_292598,RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_24981,RMVar_hsa_circ_132380,RMVar_hsa_circ_132379 88669 RMVar_ID_88669 Human_SNP_ID_11466573 m1A Human chr1 + 44339139 44339139 44339139 ACCTCTGGGGAGGGAAGGACACCATTGCCGCCATGGATGCGCCAAAGCCGTGGGCCGCCAGCTTT ACCTCTGGGGAGGGAAGGACACCATTGCCGCCGTGGATGCGCCAAAGCCGTGGGCCGCCAGCTTT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:44339101..44339239 26863196 MeRIP-seq:(Medium) rs749936233 Functional Loss SNV dbSNP153 33..33 33 - - - 88670 RMVar_ID_88670 Human_SNP_ID_11470548 m1A Human chr1 + 44355075 44355075 44355075 CGGGGCCAGCGCGGCAGGCTCCCTCCAGGTGCAGGCCCCGACGTCTCCCTCGGCCTCAGCAAGCG CGGGGCCAGCGCGGCAGGCTCCCTCCAGGTGCGGGCCCCGACGTCTCCCTCGGCCTCAGCAAGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:44354962..44355250 26863196 MeRIP-seq:(Medium) rs1238270609 Functional Loss SNV dbSNP153 33..33 33 - - - 88671 RMVar_ID_88671 Human_SNP_ID_11482408 m1A Human chr1 - 44405421 44405415 44405421 AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCAGCGGCAGCAGC AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGC______GGCGGCGGCGGCGGCAGCGGCAGCAGC CGCCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44405382..44405512 26863196 MeRIP-seq:(Medium) rs1194047152 Functional Loss DEL dbSNP153 33..38 33 - - - 88672 RMVar_ID_88672 Human_SNP_ID_11482410 m1A Human chr1 - 44405421 44405421 44405421 AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCAGCGGCAGCAGC AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44405382..44405512 26863196 MeRIP-seq:(Medium) rs1469380464 Functional Loss SNV dbSNP153 33..33 33 - - - 88673 RMVar_ID_88673 Human_SNP_ID_11484201 m1A Human chr1 + 44412084 44412084 44412084 GGGAAGACTGCTTCTTGCGTAACGCCGGCCACAGAAAGAGACTCCGATGGACTTACACCGGGCAG GGGAAGACTGCTTCTTGCGTAACGCCGGCCACGGAAAGAGACTCCGATGGACTTACACCGGGCAG A G RNF220 Ensembl:ENSG00000187147 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44412034..44412138 26863196 MeRIP-seq:(Medium) rs746352360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132401,RMVar_hsa_circ_313485 88674 RMVar_ID_88674 Human_SNP_ID_11536337 m1A Human chr1 + 44636085 44636085 44636085 GGATGATGCTGTGGACATCGAGCATGAGAACAACAACCGCTTTGAGGAGTATGAGTGGTGTGGAC GGATGATGCTGTGGACATCGAGCATGAGAACAGCAACCGCTTTGAGGAGTATGAGTGGTGTGGAC A G RNF220 Ensembl:ENSG00000187147 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:44635975..44636150 26863196 MeRIP-seq:(Medium) rs1287856205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1432015,Human_RBP_ID_1748707,Human_RBP_ID_9358771,Human_RBP_ID_11002642,Human_RBP_ID_18968239,Human_RBP_ID_21878918,Human_RBP_ID_26314111 Human_Splice_Rec_61520,Human_Splice_Rec_61521,Human_Splice_Rec_61546,Human_Splice_Rec_61547,Human_Splice_Rec_61570,Human_Splice_Rec_61571,Human_Splice_Rec_61598,Human_Splice_Rec_61604,Human_Splice_Rec_61605,Human_Splice_Rec_61618,Human_Splice_Rec_61619,Human_Splice_Rec_61634,Human_Splice_Rec_61635,Human_Splice_Rec_61650,Human_Splice_Rec_61651,Human_Splice_Rec_61660,Human_Splice_Rec_61664,Human_Splice_Rec_61665,Human_Splice_Rec_61672,Human_Splice_Rec_61673,Human_Splice_Rec_61688,Human_Splice_Rec_61689 RMVar_hsa_circ_15965,RMVar_hsa_circ_62880,RMVar_hsa_circ_334205,RMVar_hsa_circ_105978,RMVar_hsa_circ_43671,RMVar_hsa_circ_132405 88675 RMVar_ID_88675 Human_SNP_ID_11537827 m1A Human chr1 - 44642384 44642384 44642384 ACACAGAGCAGCTGCTCTCTAAATCCCTGCTAAAGGAAAGAACTCTCACCTCAATGCCATTCTTT ACACAGAGCAGCTGCTCTCTAAATCCCTGCTATAGGAAAGAACTCTCACCTCAATGCCATTCTTT T A TMEM53 Ensembl:ENSG00000126106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44642380..44642609 26863196 MeRIP-seq:(Medium) rs1228421480 Functional Loss SNV dbSNP153 33..33 33 - - - 88676 RMVar_ID_88676 Human_SNP_ID_11539442 m1A Human chr1 + 44649015 44649014 44649015 TGAATGATGAGGCAGAGCTAGTGAGTCAGGCGAGGGGGTGCAGAGGGATCACAGTGCAGAGGCCA TGAATGATGAGGCAGAGCTAGTGAGTCAGGCG_GGGGGTGCAGAGGGATCACAGTGCAGAGGCCA GA G RNF220 Ensembl:ENSG00000187147 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44649014..44649115 26863196 MeRIP-seq:(Medium) rs1044641887 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_62880,RMVar_hsa_circ_18314 88677 RMVar_ID_88677 Human_SNP_ID_11540002 m1A Human chr1 + 44650814 44650814 44650814 TGCCCCAGGCAGGCCTCGCCTCCAGCAGCCCCACCTGCCCCCAGCCTCTGTGACAGTGACCGTCT TGCCCCAGGCAGGCCTCGCCTCCAGCAGCCCCCCCTGCCCCCAGCCTCTGTGACAGTGACCGTCT A C RNF220 Ensembl:ENSG00000187147 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44650764..44650903 26863196 MeRIP-seq:(Medium) rs757612310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1417079,Human_miRNA_ID_1700884 88678 RMVar_ID_88678 Human_SNP_ID_11540086 m1A Human chr1 + 44651158 44651158 44651158 CCAGACTGAAGCACATGTAATATAGACCGTGTATGTTTACAATGTTGTGTATAAATGGGACAACT CCAGACTGAAGCACATGTAATATAGACCGTGTGTGTTTACAATGTTGTGTATAAATGGGACAACT A G RNF220 Ensembl:ENSG00000187147 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44651109..44651329 26863196 MeRIP-seq:(Medium) rs924945851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356184,Human_RBP_ID_1432022,Human_RBP_ID_1748710,Human_RBP_ID_2149462,Human_RBP_ID_11002946,Human_RBP_ID_21878924,Human_RBP_ID_23397813 Human_miRNA_ID_1712458 88679 RMVar_ID_88679 Human_SNP_ID_11540087 m1A Human chr1 + 44651158 44651158 44651158 CCAGACTGAAGCACATGTAATATAGACCGTGTATGTTTACAATGTTGTGTATAAATGGGACAACT CCAGACTGAAGCACATGTAATATAGACCGTGTTTGTTTACAATGTTGTGTATAAATGGGACAACT A T RNF220 Ensembl:ENSG00000187147 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44651109..44651329 26863196 MeRIP-seq:(Medium) rs924945851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356184,Human_RBP_ID_1432022,Human_RBP_ID_1748710,Human_RBP_ID_2149462,Human_RBP_ID_11002946,Human_RBP_ID_21878924,Human_RBP_ID_23397813 Human_miRNA_ID_1712458 88680 RMVar_ID_88680 Human_SNP_ID_11540177 m1A Human chr1 - 44651566 44651566 44651566 ACTTTTTCCCTGGGAAAGGCAGCTCTAATCCCAGGAATGGTTCTCAGCAGAGGCTGGGTGGCCAG ACTTTTTCCCTGGGAAAGGCAGCTCTAATCCCGGGAATGGTTCTCAGCAGAGGCTGGGTGGCCAG T C TMEM53 Ensembl:ENSG00000126106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44651516..44651605 26863196 MeRIP-seq:(Medium) rs997561973 Functional Loss SNV dbSNP153 33..33 33 - - - 88681 RMVar_ID_88681 Human_SNP_ID_11547203 m1A Human chr1 - 44681583 44681583 44681583 CACCCCGCCTTCTCAGGGCCCTCATTCTACTCATTACTCCTGCCTCCCTTGTATCCTTAACCCCT CACCCCGCCTTCTCAGGGCCCTCATTCTACTCGTTACTCCTGCCTCCCTTGTATCCTTAACCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44681534..44681697 26863196 MeRIP-seq:(Medium) rs560558175 Functional Loss SNV dbSNP153 33..33 33 - - - 88682 RMVar_ID_88682 Human_SNP_ID_11547204 m1A Human chr1 - 44681583 44681583 44681583 CACCCCGCCTTCTCAGGGCCCTCATTCTACTCATTACTCCTGCCTCCCTTGTATCCTTAACCCCT CACCCCGCCTTCTCAGGGCCCTCATTCTACTCCTTACTCCTGCCTCCCTTGTATCCTTAACCCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44681534..44681697 26863196 MeRIP-seq:(Medium) rs560558175 Functional Loss SNV dbSNP153 33..33 33 - - - 88683 RMVar_ID_88683 Human_SNP_ID_11556921 m1A Human chr1 + 44721801 44721801 44721801 TTAGTAACAGAACATTCAGCCTTGCCTAGGCAAGACTTCAAAAAATTTAACCATAAACTCATAGT TTAGTAACAGAACATTCAGCCTTGCCTAGGCAGGACTTCAAAAAATTTAACCATAAACTCATAGT A G ARMH1 Ensembl:ENSG00000198520 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:44721751..44721825 26863196 MeRIP-seq:(Medium) rs1441995791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108849,RMVar_hsa_circ_132408 88684 RMVar_ID_88684 Human_SNP_ID_11556929 m1A Human chr1 - 44721805 44721805 44721805 AACAACTATGAGTTTATGGTTAAATTTTTTGAAGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA AACAACTATGAGTTTATGGTTAAATTTTTTGATGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA T A RNU5F-1 Ensembl:ENSG00000199377 snRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44721756..44721874 26863196 MeRIP-seq:(Medium) rs779336665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269175,Human_RBP_ID_272928,Human_RBP_ID_356205,Human_RBP_ID_1154754,Human_RBP_ID_1233816,Human_RBP_ID_1256077,Human_RBP_ID_1348778,Human_RBP_ID_1432029,Human_RBP_ID_1748716,Human_RBP_ID_2149477,Human_RBP_ID_3314222,Human_RBP_ID_5156131,Human_RBP_ID_5254193,Human_RBP_ID_5829699,Human_RBP_ID_8048899,Human_RBP_ID_8244310,Human_RBP_ID_8312424,Human_RBP_ID_8725006,Human_RBP_ID_8749726,Human_RBP_ID_9319975,Human_RBP_ID_9340548,Human_RBP_ID_9412981,Human_RBP_ID_9523031,Human_RBP_ID_10481985,Human_RBP_ID_11003006,Human_RBP_ID_16976076,Human_RBP_ID_17182908,Human_RBP_ID_17224486,Human_RBP_ID_17456937,Human_RBP_ID_17672894,Human_RBP_ID_17678032,Human_RBP_ID_17752288,Human_RBP_ID_18197981,Human_RBP_ID_18204818,Human_RBP_ID_18524469,Human_RBP_ID_18544029,Human_RBP_ID_18575983,Human_RBP_ID_19369159,Human_RBP_ID_21963854,Human_RBP_ID_22144052,Human_RBP_ID_22531369,Human_RBP_ID_22536469,Human_RBP_ID_22785141,Human_RBP_ID_22864630,Human_RBP_ID_23110155,Human_RBP_ID_23111017,Human_RBP_ID_23149660,Human_RBP_ID_23263472,Human_RBP_ID_23426016,Human_RBP_ID_24397480,Human_RBP_ID_24452942,Human_RBP_ID_24541895,Human_RBP_ID_24550593,Human_RBP_ID_24556679,Human_RBP_ID_24700799,Human_RBP_ID_26588031,Human_RBP_ID_26746953,Human_RBP_ID_26865545,Human_RBP_ID_27183914,Human_RBP_ID_27399264,Human_RBP_ID_27571612 Human_miRNA_ID_3132828 88685 RMVar_ID_88685 Human_SNP_ID_11556930 m1A Human chr1 - 44721805 44721805 44721805 AACAACTATGAGTTTATGGTTAAATTTTTTGAAGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA AACAACTATGAGTTTATGGTTAAATTTTTTGAGGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA T C RNU5F-1 Ensembl:ENSG00000199377 snRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44721756..44721874 26863196 MeRIP-seq:(Medium) rs779336665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269175,Human_RBP_ID_272928,Human_RBP_ID_356205,Human_RBP_ID_1154754,Human_RBP_ID_1233816,Human_RBP_ID_1256077,Human_RBP_ID_1348778,Human_RBP_ID_1432029,Human_RBP_ID_1748716,Human_RBP_ID_2149477,Human_RBP_ID_3314222,Human_RBP_ID_5156131,Human_RBP_ID_5254193,Human_RBP_ID_5829699,Human_RBP_ID_8048899,Human_RBP_ID_8244310,Human_RBP_ID_8312424,Human_RBP_ID_8725006,Human_RBP_ID_8749726,Human_RBP_ID_9319975,Human_RBP_ID_9340548,Human_RBP_ID_9412981,Human_RBP_ID_9523031,Human_RBP_ID_10481985,Human_RBP_ID_11003006,Human_RBP_ID_16976076,Human_RBP_ID_17182908,Human_RBP_ID_17224486,Human_RBP_ID_17456937,Human_RBP_ID_17672894,Human_RBP_ID_17678032,Human_RBP_ID_17752288,Human_RBP_ID_18197981,Human_RBP_ID_18204818,Human_RBP_ID_18524469,Human_RBP_ID_18544029,Human_RBP_ID_18575983,Human_RBP_ID_19369159,Human_RBP_ID_21963854,Human_RBP_ID_22144052,Human_RBP_ID_22531369,Human_RBP_ID_22536469,Human_RBP_ID_22785141,Human_RBP_ID_22864630,Human_RBP_ID_23110155,Human_RBP_ID_23111017,Human_RBP_ID_23149660,Human_RBP_ID_23263472,Human_RBP_ID_23426016,Human_RBP_ID_24397480,Human_RBP_ID_24452942,Human_RBP_ID_24541895,Human_RBP_ID_24550593,Human_RBP_ID_24556679,Human_RBP_ID_24700799,Human_RBP_ID_26588031,Human_RBP_ID_26746953,Human_RBP_ID_26865545,Human_RBP_ID_27183914,Human_RBP_ID_27399264,Human_RBP_ID_27571612 Human_miRNA_ID_3132828 88686 RMVar_ID_88686 Human_SNP_ID_11556931 m1A Human chr1 - 44721805 44721805 44721805 AACAACTATGAGTTTATGGTTAAATTTTTTGAAGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA AACAACTATGAGTTTATGGTTAAATTTTTTGACGTCTTGCCTAGGCAAGGCTGAATGTTCTGTTA T G RNU5F-1 Ensembl:ENSG00000199377 snRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44721756..44721874 26863196 MeRIP-seq:(Medium) rs779336665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269175,Human_RBP_ID_272928,Human_RBP_ID_356205,Human_RBP_ID_1154754,Human_RBP_ID_1233816,Human_RBP_ID_1256077,Human_RBP_ID_1348778,Human_RBP_ID_1432029,Human_RBP_ID_1748716,Human_RBP_ID_2149477,Human_RBP_ID_3314222,Human_RBP_ID_5156131,Human_RBP_ID_5254193,Human_RBP_ID_5829699,Human_RBP_ID_8048899,Human_RBP_ID_8244310,Human_RBP_ID_8312424,Human_RBP_ID_8725006,Human_RBP_ID_8749726,Human_RBP_ID_9319975,Human_RBP_ID_9340548,Human_RBP_ID_9412981,Human_RBP_ID_9523031,Human_RBP_ID_10481985,Human_RBP_ID_11003006,Human_RBP_ID_16976076,Human_RBP_ID_17182908,Human_RBP_ID_17224486,Human_RBP_ID_17456937,Human_RBP_ID_17672894,Human_RBP_ID_17678032,Human_RBP_ID_17752288,Human_RBP_ID_18197981,Human_RBP_ID_18204818,Human_RBP_ID_18524469,Human_RBP_ID_18544029,Human_RBP_ID_18575983,Human_RBP_ID_19369159,Human_RBP_ID_21963854,Human_RBP_ID_22144052,Human_RBP_ID_22531369,Human_RBP_ID_22536469,Human_RBP_ID_22785141,Human_RBP_ID_22864630,Human_RBP_ID_23110155,Human_RBP_ID_23111017,Human_RBP_ID_23149660,Human_RBP_ID_23263472,Human_RBP_ID_23426016,Human_RBP_ID_24397480,Human_RBP_ID_24452942,Human_RBP_ID_24541895,Human_RBP_ID_24550593,Human_RBP_ID_24556679,Human_RBP_ID_24700799,Human_RBP_ID_26588031,Human_RBP_ID_26746953,Human_RBP_ID_26865545,Human_RBP_ID_27183914,Human_RBP_ID_27399264,Human_RBP_ID_27571612 Human_miRNA_ID_3132828 88687 RMVar_ID_88687 Human_SNP_ID_11562648 m1A Human chr1 - 44738613 44738613 44738613 GAGTGGCTCCTCACTTCTCAGACGGGGCGGCCAGTCAGAGACGATCCTCACCTCCCAGACAGGGT GAGTGGCTCCTCACTTCTCAGACGGGGCGGCCGGTCAGAGACGATCCTCACCTCCCAGACAGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44738436..44738703 26863196 MeRIP-seq:(Medium) rs1422031591 Functional Loss SNV dbSNP153 33..33 33 - - - 88688 RMVar_ID_88688 Human_SNP_ID_11563566 m1A Human chr1 + 44740879 44740879 44740879 GTGGAATCCTAAAAGTGAAGCTCTCAGGAAAGAGATGGGTAACTCTGGTTTTTTCATACTTTATA GTGGAATCCTAAAAGTGAAGCTCTCAGGAAAGCGATGGGTAACTCTGGTTTTTTCATACTTTATA A C KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44740878..44740944 26863196 MeRIP-seq:(Medium) rs750123116 Functional Loss SNV dbSNP153 33..33 33 - - - 88689 RMVar_ID_88689 Human_SNP_ID_11568634 m1A Human chr1 + 44759288 44759288 44759288 CAAGCAACAGGTGCAAGTGGTGGGGCTGCAGGAGCATCTGGTTAACTCTGCTGATGATGTCATCA CAAGCAACAGGTGCAAGTGGTGGGGCTGCAGGCGCATCTGGTTAACTCTGCTGATGATGTCATCA A C KIF2C Ensembl:ENSG00000142945 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:44756234..44759305 32194978 MeRIP-seq:(Medium) rs1420725626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1748733,Human_RBP_ID_5829776,Human_RBP_ID_8749743 Human_Splice_Rec_62020,Human_Splice_Rec_62021,Human_Splice_Rec_62084,Human_Splice_Rec_62085 Human_miRNA_ID_2618494 RMVar_hsa_circ_98107,RMVar_hsa_circ_132411,RMVar_hsa_circ_51082,RMVar_hsa_circ_65529,RMVar_hsa_circ_357232,RMVar_hsa_circ_309739,RMVar_hsa_circ_132418,RMVar_hsa_circ_41413,RMVar_hsa_circ_113844,RMVar_hsa_circ_282448,RMVar_hsa_circ_318743,RMVar_hsa_circ_50143,RMVar_hsa_circ_132424,RMVar_hsa_circ_132422,RMVar_hsa_circ_132423,RMVar_hsa_circ_132421,RMVar_hsa_circ_35822,RMVar_hsa_circ_372155,RMVar_hsa_circ_132425,RMVar_hsa_circ_374932 88690 RMVar_ID_88690 Human_SNP_ID_11573359 m1A Human chr1 + 44776139 44776139 44776139 GTATGAGTTGGGGCGCCCAGCTGCCAACACCAAGGTGGGTGCGAGCGTGGGCCTGTCCGCCTGGG GTATGAGTTGGGGCGCCCAGCTGCCAACACCAGGGTGGGTGCGAGCGTGGGCCTGTCCGCCTGGG A G RPS8 Ensembl:ENSG00000142937 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:44776098..44776213 26863196 MeRIP-seq:(Medium) rs1437691570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356235,Human_RBP_ID_857046,Human_RBP_ID_8970667,Human_RBP_ID_17456453,Human_RBP_ID_17752310,Human_RBP_ID_19038016,Human_RBP_ID_19369262,Human_RBP_ID_26311147,Human_RBP_ID_26798301,Human_RBP_ID_26865571 Human_Splice_Rec_62121,Human_Splice_Rec_62129,Human_Splice_Rec_62139,Human_Splice_Rec_62149,Human_Splice_Rec_62151 RMVar_hsa_circ_97389,RMVar_hsa_circ_115120,RMVar_hsa_circ_117122,RMVar_hsa_circ_132426,RMVar_hsa_circ_132427,RMVar_hsa_circ_323355,RMVar_hsa_circ_354694,RMVar_hsa_circ_132428 88691 RMVar_ID_88691 Human_SNP_ID_11573578 m1A Human chr1 - 44776774 44776774 44776774 TTTCCCACCCACTCCCAAAGGGCCTCACTCACACTCTGAGCCCCAGGAGAAATTCCCCACGTCCA TTTCCCACCCACTCCCAAAGGGCCTCACTCACCCTCTGAGCCCCAGGAGAAATTCCCCACGTCCA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:44776625..44776837 26863410 MeRIP-seq:(Medium) rs756591403 Functional Loss SNV dbSNP153 33..33 33 - - - 88692 RMVar_ID_88692 Human_SNP_ID_11573872 m1A Human chr1 + 44777723 44777723 44777723 GTGAAGAATTGCATCGTGCTCATCGACAGCACACCGTACCGACAGTGGTACGAGTCCCACTATGC GTGAAGAATTGCATCGTGCTCATCGACAGCACGCCGTACCGACAGTGGTACGAGTCCCACTATGC A G RPS8 Ensembl:ENSG00000142937 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44777675..44777764 26863196 MeRIP-seq:(Medium) rs995974053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20695,Human_RBP_ID_356244,Human_RBP_ID_857050,Human_RBP_ID_1432075,Human_RBP_ID_1748761,Human_RBP_ID_2149545,Human_RBP_ID_4055427,Human_RBP_ID_8312489,Human_RBP_ID_8970672,Human_RBP_ID_11214384,Human_RBP_ID_17218806,Human_RBP_ID_17678043,Human_RBP_ID_17752314,Human_RBP_ID_18576051,Human_RBP_ID_22021139,Human_RBP_ID_22144095,Human_RBP_ID_22785170,Human_RBP_ID_23149675,Human_RBP_ID_23397961,Human_RBP_ID_26390991,Human_RBP_ID_26588043,Human_RBP_ID_26798317,Human_RBP_ID_26865591,Human_RBP_ID_27183943,Human_RBP_ID_27399297 Human_Splice_Rec_62125,Human_Splice_Rec_62133,Human_Splice_Rec_62143,Human_Splice_Rec_62155,Human_Splice_Rec_62159,Human_Splice_Rec_62163 RMVar_hsa_circ_97389,RMVar_hsa_circ_115120,RMVar_hsa_circ_117122,RMVar_hsa_circ_132426,RMVar_hsa_circ_132427,RMVar_hsa_circ_354694,RMVar_hsa_circ_114196,RMVar_hsa_circ_132428,RMVar_hsa_circ_50883,RMVar_hsa_circ_75992,RMVar_hsa_circ_103338,RMVar_hsa_circ_132430,RMVar_hsa_circ_92960,RMVar_hsa_circ_132432,RMVar_hsa_circ_132433,RMVar_hsa_circ_132431 88693 RMVar_ID_88693 Human_SNP_ID_11574176 m1A Human chr1 + 44778537 44778537 44778537 TCTTAAGCGGGTGGAGAGGTTTGGGTAGGGCCACCTTGTCGTTGTGCTAAGGATCACCTACTCTC TCTTAAGCGGGTGGAGAGGTTTGGGTAGGGCCGCCTTGTCGTTGTGCTAAGGATCACCTACTCTC A G RPS8 Ensembl:ENSG00000142937 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44778532..44778701 26863196 MeRIP-seq:(Medium) rs766129139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356270,Human_RBP_ID_1432094,Human_RBP_ID_3314284,Human_RBP_ID_5335409,Human_RBP_ID_8312504,Human_RBP_ID_8970684,Human_RBP_ID_11003494,Human_RBP_ID_18158010,Human_RBP_ID_18576066,Human_RBP_ID_22535222,Human_RBP_ID_22563140,Human_RBP_ID_22633625,Human_RBP_ID_22785180,Human_RBP_ID_23397984,Human_RBP_ID_26774336,Human_RBP_ID_26865607 RMVar_hsa_circ_97389,RMVar_hsa_circ_117122,RMVar_hsa_circ_132427,RMVar_hsa_circ_114196,RMVar_hsa_circ_132428,RMVar_hsa_circ_75992,RMVar_hsa_circ_132430,RMVar_hsa_circ_88034,RMVar_hsa_circ_132431,RMVar_hsa_circ_132434 88694 RMVar_ID_88694 Human_SNP_ID_11574198 m1A Human chr1 - 44778578 44778578 44778578 TCGGCCACACTGTCCCGGCCTTGAAGCGATGCACGCTGCAAGAGAGTAGGTGATCCTTAGCACAA TCGGCCACACTGTCCCGGCCTTGAAGCGATGCCCGCTGCAAGAGAGTAGGTGATCCTTAGCACAA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:44778576..44778725 32194978 MeRIP-seq:(Medium) rs1165172028 Functional Loss SNV dbSNP153 33..33 33 - - - 88695 RMVar_ID_88695 Human_SNP_ID_11582027 m1A Human chr1 + 44800595 44800595 44800595 CGCGGACCTGAGCTGGAGATGCTGGCCGGGCTACCGACGTCAGACCCCGGGCGCCTCATCACGGA CGCGGACCTGAGCTGGAGATGCTGGCCGGGCTGCCGACGTCAGACCCCGGGCGCCTCATCACGGA A G PLK3 Ensembl:ENSG00000173846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44800038..44800601 26863196 MeRIP-seq:(Medium) rs372090200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27399313 Human_Splice_Rec_62183,Human_Splice_Rec_62211 RMVar_hsa_circ_78049,RMVar_hsa_circ_132436 88696 RMVar_ID_88696 Human_SNP_ID_11628354 m1A Human chr1 - 44986468 44986467 44986468 TGACCCGGGTGAGCAGTGCGGTGGGGCCACTCATCTGAGGGAGGCGGGCATGTCGAACTGGGCCG TGACCCGGGTGAGCAGTGCGGTGGGGCCACTC_TCTGAGGGAGGCGGGCATGTCGAACTGGGCCG AT A EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:44986465..44986575 26863410 MeRIP-seq:(Medium) rs1253047386 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82339,RMVar_hsa_circ_84631,RMVar_hsa_circ_132461,RMVar_hsa_circ_132464 88697 RMVar_ID_88697 Human_SNP_ID_11628384 m1A Human chr1 + 44986543 44986543 44986543 GTGCGGCCTGGCAGGGCAGAAGTCACAGCTATAACTCAGCTCCCGGCACGCCGCAACCGCTCCCA GTGCGGCCTGGCAGGGCAGAAGTCACAGCTATTACTCAGCTCCCGGCACGCCGCAACCGCTCCCA A T RF00017-049,lnc-UROD-1 RNACentral:URS000096B6E3,RNACentral:URS00008BAB63 SRP RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44986452..44986600 26863196 MeRIP-seq:(Medium) rs1023199976 Functional Loss SNV dbSNP153 33..33 33 - - - 88698 RMVar_ID_88698 Human_SNP_ID_61817993 m1A Human chr2 + 15528111 15528111 15528111 CTCTACAGTATCAGCCAAGCTACACCACTTACAATTTCCCAAAACTACACTATGACTTCTTTTCC CTCTACAGTATCAGCCAAGCTACACCACTTACGATTTCCCAAAACTACACTATGACTTCTTTTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:15527984..15528141 26863196 MeRIP-seq:(Medium) rs1376865628 Functional Loss SNV dbSNP153 33..33 33 - - - 88699 RMVar_ID_88699 Human_SNP_ID_61833821 m1A Human chr2 + 15591934 15591934 15591934 GAGCAGGCGAAGCCGCGGAGGACGGGGTGAAGATGGCGGCCTTCTCCGGTGCGTTTGTGGAAACT GAGCAGGCGAAGCCGCGGAGGACGGGGTGAAGTTGGCGGCCTTCTCCGGTGCGTTTGTGGAAACT A T DDX1 Ensembl:ENSG00000079785 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:15591896..15592045 26863196 MeRIP-seq:(Medium) rs1332724275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56608,Human_RBP_ID_242271,Human_RBP_ID_827246,Human_RBP_ID_915301,Human_RBP_ID_4623123,Human_RBP_ID_5117823,Human_RBP_ID_8851050,Human_RBP_ID_9296365,Human_RBP_ID_18421695,Human_RBP_ID_19096933,Human_RBP_ID_27002046 Human_Splice_Rec_219723,Human_Splice_Rec_219773,Human_Splice_Rec_219775,Human_Splice_Rec_219817 RMVar_hsa_circ_121769,RMVar_hsa_circ_197258 88700 RMVar_ID_88700 Human_SNP_ID_61834759 m1A Human chr2 - 15595541 15595541 15595541 CTCACCAAATTTAAACTTACCATAAGTACATCACCTCCTCCTAAGATCAATGGGATAGATTCAGC CTCACCAAATTTAAACTTACCATAAGTACATCGCCTCCTCCTAAGATCAATGGGATAGATTCAGC T C lnc-NBAS-8 RNACentral:URS00008B7763 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:15595476..15595575 26863196 MeRIP-seq:(Medium) rs1378373697 Functional Loss SNV dbSNP153 33..33 33 - - - 88701 RMVar_ID_88701 Human_SNP_ID_61834761 m1A Human chr2 - 15595552 15595552 15595552 CTACCAATCACCTCACCAAATTTAAACTTACCATAAGTACATCACCTCCTCCTAAGATCAATGGG CTACCAATCACCTCACCAAATTTAAACTTACCGTAAGTACATCACCTCCTCCTAAGATCAATGGG T C lnc-NBAS-8 RNACentral:URS00008B7763 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:15595437..15595610 26863196 MeRIP-seq:(Medium) rs1466514648 Functional Loss SNV dbSNP153 33..33 33 - - - 88702 RMVar_ID_88702 Human_SNP_ID_61835033 m1A Human chr2 + 15596728 15596725 15596729 ACTTAATCTGTAAAATCAACTTTTTTCCCCTCATTCAGGCTGCAGAAACAGGAAGTGGCAAAACT ACTTAATCTGTAAAATCAACTTTTTTCCCC____TCAGGCTGCAGAAACAGGAAGTGGCAAAACT CTCAT C DDX1 Ensembl:ENSG00000079785 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:15596726..15596750 26863196 MeRIP-seq:(Medium) rs1446786412 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_922540,Human_RBP_ID_2596284,Human_RBP_ID_5378230,Human_RBP_ID_9347072,Human_RBP_ID_13650949,Human_RBP_ID_19096938,Human_RBP_ID_22667030,Human_RBP_ID_25574476 Human_Splice_Rec_219729,Human_Splice_Rec_219823 RMVar_hsa_circ_1836,RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_371153,RMVar_hsa_circ_344483,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197263,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_360164,RMVar_hsa_circ_197265,RMVar_hsa_circ_19463 88703 RMVar_ID_88703 Human_SNP_ID_61835035 m1A Human chr2 + 15596745 15596745 15596745 AACTTTTTTCCCCTCATTCAGGCTGCAGAAACAGGAAGTGGCAAAACTGGTGTAAGTAATAAATT AACTTTTTTCCCCTCATTCAGGCTGCAGAAACTGGAAGTGGCAAAACTGGTGTAAGTAATAAATT A T DDX1 Ensembl:ENSG00000079785 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:15596726..15596775 26863196 MeRIP-seq:(Medium) rs766867235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_922540,Human_RBP_ID_3958685,Human_RBP_ID_5378230,Human_RBP_ID_9347072,Human_RBP_ID_13650949,Human_RBP_ID_19096938,Human_RBP_ID_22667030,Human_RBP_ID_23211448,Human_RBP_ID_25574476,Human_RBP_ID_26786784 Human_Splice_Rec_219728,Human_Splice_Rec_219729,Human_Splice_Rec_219822,Human_Splice_Rec_219823 RMVar_hsa_circ_1836,RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_371153,RMVar_hsa_circ_344483,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197263,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_360164,RMVar_hsa_circ_197265,RMVar_hsa_circ_19463 88704 RMVar_ID_88704 Human_SNP_ID_61835198 m1A Human chr2 + 15597457 15597457 15597457 ACAGGAAGGCAAAAAAGGAAAAACAACAATTAAAACTGGTGCTTCAGGTAATTTTTGTAAATTGA ACAGGAAGGCAAAAAAGGAAAAACAACAATTAGAACTGGTGCTTCAGGTAATTTTTGTAAATTGA A G DDX1 Ensembl:ENSG00000079785 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:15597364..15597518 26863196 MeRIP-seq:(Medium) rs553463267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2596294,Human_RBP_ID_19099369,Human_RBP_ID_22764893,Human_RBP_ID_27475450 Human_Splice_Rec_219730,Human_Splice_Rec_219731,Human_Splice_Rec_219824,Human_Splice_Rec_219825 Human_miRNA_ID_744085,Human_miRNA_ID_2299147,Human_miRNA_ID_2302418,Human_miRNA_ID_2305682 RMVar_hsa_circ_1836,RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_371153,RMVar_hsa_circ_344483,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_17755,RMVar_hsa_circ_98788,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197263,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_360164,RMVar_hsa_circ_197265,RMVar_hsa_circ_19463,RMVar_hsa_circ_352235,RMVar_hsa_circ_360903,RMVar_hsa_circ_327507,RMVar_hsa_circ_60659,RMVar_hsa_circ_69037,RMVar_hsa_circ_23533,RMVar_hsa_circ_197266 88705 RMVar_ID_88705 Human_SNP_ID_61836632 m1A Human chr2 + 15603270 15603270 15603270 GGTCGGGTGGTCTACCATGCAGGCCTCTTTGGACCTAGGTAAGTGTTTCTAAAATAACTGAATTG GGTCGGGTGGTCTACCATGCAGGCCTCTTTGGGCCTAGGTAAGTGTTTCTAAAATAACTGAATTG A G DDX1 Ensembl:ENSG00000079785 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:15602610..15604454 26863410 MeRIP-seq:(Medium) rs1297315212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2596377,Human_RBP_ID_5380611 Human_Splice_Rec_219736,Human_Splice_Rec_219737,Human_Splice_Rec_219780,Human_Splice_Rec_219781,Human_Splice_Rec_219830,Human_Splice_Rec_219831,Human_Splice_Rec_219870,Human_Splice_Rec_219871 RMVar_hsa_circ_1836,RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_371153,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_17755,RMVar_hsa_circ_98788,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197263,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_197265,RMVar_hsa_circ_352235,RMVar_hsa_circ_360903,RMVar_hsa_circ_69037,RMVar_hsa_circ_23533,RMVar_hsa_circ_63311,RMVar_hsa_circ_121495,RMVar_hsa_circ_197266,RMVar_hsa_circ_197267,RMVar_hsa_circ_281691,RMVar_hsa_circ_50973,RMVar_hsa_circ_197269 88706 RMVar_ID_88706 Human_SNP_ID_61836634 m1A Human chr2 - 15603273 15603273 15603273 AATCAATTCAGTTATTTTAGAAACACTTACCTAGGTCCAAAGAGGCCTGCATGGTAGACCACCCG AATCAATTCAGTTATTTTAGAAACACTTACCTGGGTCCAAAGAGGCCTGCATGGTAGACCACCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:15603176..15603300;chr2:15603176..15603369 26863196 MeRIP-seq:(Medium) rs1486988796 Functional Loss SNV dbSNP153 33..33 33 - - - 88707 RMVar_ID_88707 Human_SNP_ID_61836766 m1A Human chr2 - 15603805 15603805 15603805 AGCCAAATCCAAACTTGTCAGTACCTAGATTTAAAAAATATTTTACTTTTCTGGTAAGAGAAAAT AGCCAAATCCAAACTTGTCAGTACCTAGATTTTAAAAATATTTTACTTTTCTGGTAAGAGAAAAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:15603801..15603825 26863196 MeRIP-seq:(Medium) rs778551487 Functional Loss SNV dbSNP153 33..33 33 - - - 88708 RMVar_ID_88708 Human_SNP_ID_61856927 m1A Human chr2 + 15681166 15681165 15681166 GGGAGGGGAGGGGGAGGGGGGAGGGGAGGGGGAGGGGGGAGGGGGAGGGGTGGGGGAGGGGGAGG GGGAGGGGAGGGGGAGGGGGGAGGGGAGGGGG_GGGGGGAGGGGGAGGGGTGGGGGAGGGGGAGG GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:15681046..15681174 26863196 MeRIP-seq:(Medium) rs1558472431 Functional Loss DEL dbSNP153 33..33 33 - - - 88709 RMVar_ID_88709 Human_SNP_ID_61856928 m1A Human chr2 + 15681166 15681166 15681166 GGGAGGGGAGGGGGAGGGGGGAGGGGAGGGGGAGGGGGGAGGGGGAGGGGTGGGGGAGGGGGAGG GGGAGGGGAGGGGGAGGGGGGAGGGGAGGGGGGGGGGGGAGGGGGAGGGGTGGGGGAGGGGGAGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:15681046..15681174 26863196 MeRIP-seq:(Medium) rs1214619686 Functional Loss SNV dbSNP153 33..33 33 - - - 88710 RMVar_ID_88710 Human_SNP_ID_62365178 m1A Human chr2 - 17753356 17753356 17753356 AACCTGGCGTCTGCTCCGGGCCGTCCCCTCCCAGGCGGCCGTCCCCTCCCAGGCGGCCGTCCCCA AACCTGGCGTCTGCTCCGGGCCGTCCCCTCCCGGGCGGCCGTCCCCTCCCAGGCGGCCGTCCCCA T C SMC6 Ensembl:ENSG00000163029 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:17753349..17753445 26863196 MeRIP-seq:(Medium) rs1407052419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777316,Human_RBP_ID_5322020,Human_RBP_ID_5380614,Human_RBP_ID_17084442,Human_RBP_ID_26786515 88711 RMVar_ID_88711 Human_SNP_ID_62365236 m1A Human chr2 + 17753460 17753460 17753460 GCGAAGGTGCCGCCGGCCGCCCGACCCGCCCGAGGAACGGACATCTCCCGCCCGGGCCCGCAAGG GCGAAGGTGCCGCCGGCCGCCCGACCCGCCCGTGGAACGGACATCTCCCGCCCGGGCCCGCAAGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:17753411..17753589 26863196 MeRIP-seq:(Medium) rs1003166808 Functional Loss SNV dbSNP153 33..33 33 - - - 88712 RMVar_ID_88712 Human_SNP_ID_62365360 m1A Human chr2 - 17753771 17753771 17753771 ACCGCGGTGGGCGCCGGGGCTCCCGGGAATCTACCTTCTCCTGCGGCCGGCACGCGGTTCCCAGG ACCGCGGTGGGCGCCGGGGCTCCCGGGAATCTGCCTTCTCCTGCGGCCGGCACGCGGTTCCCAGG T C SMC6 Ensembl:ENSG00000163029 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:17753348..17753787 26863196 MeRIP-seq:(Medium) rs3747514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4588768,Human_RBP_ID_5444277,Human_RBP_ID_5501344,Human_RBP_ID_8851056,Human_RBP_ID_9297050,Human_RBP_ID_9386100,Human_RBP_ID_18421698,Human_RBP_ID_18493252 88713 RMVar_ID_88713 Human_SNP_ID_62568101 m1A Human chr2 - 18560331 18560306 18560331 GATCATGGGCTGCCGGGACCGCGCGCGCGCCGAGGAGGCGGCGGGTCAGCTCCGCCGCGAGCTCC GATCATGGGCTGCCGGGACCGCGCGCGCGCCG_________________________CGAGCTCC GCGGCGGAGCTGACCCGCCGCCTCCT G NT5C1B-RDH14,RDH14 Ensembl:ENSG00000250741,Ensembl:ENSG00000240857 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:18560282..18560383 32194978 MeRIP-seq:(Medium) rs1558357616 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_244047,Human_RBP_ID_4622223 88714 RMVar_ID_88714 Human_SNP_ID_62568176 m1A Human chr2 - 18560428 18560428 18560428 CCGGCCTCATGCACGGGAAGACTGTGCTGATCACCGGGGCGAACAGCGGCCTGGGCCGCGCCACG CCGGCCTCATGCACGGGAAGACTGTGCTGATCGCCGGGGCGAACAGCGGCCTGGGCCGCGCCACG T C NT5C1B-RDH14,RDH14 Ensembl:ENSG00000250741,Ensembl:ENSG00000240857 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:18560378..18560630 26863196 MeRIP-seq:(Medium) rs767202026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624044,Human_RBP_ID_18421700 88715 RMVar_ID_88715 Human_SNP_ID_62568280 m1A Human chr2 - 18560600 18560589 18560600 CCGGTAAGGCGGCGGCTGCGGAACTCCCGTGGAGGGGCCGGTGGGCCCTCGGGCCTGACGATGGC CCGGTAAGGCGGCGGCTGCGGAACTCCCGTGG___________GGCCCTCGGGCCTGACGATGGC CCACCGGCCCCT C NT5C1B-RDH14,RDH14 Ensembl:ENSG00000250741,Ensembl:ENSG00000240857 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:18560282..18560680;chr2:18560362..18560638 26863196 MeRIP-seq:(Medium) rs1255383747 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_244049,Human_RBP_ID_777627,Human_RBP_ID_4622225,Human_RBP_ID_5501389 88716 RMVar_ID_88716 Human_SNP_ID_62568292 m1A Human chr2 - 18560611 18560611 18560611 TCTCTTGGGTTCCGGTAAGGCGGCGGCTGCGGAACTCCCGTGGAGGGGCCGGTGGGCCCTCGGGC TCTCTTGGGTTCCGGTAAGGCGGCGGCTGCGGGACTCCCGTGGAGGGGCCGGTGGGCCCTCGGGC T C NT5C1B-RDH14,RDH14 Ensembl:ENSG00000250741,Ensembl:ENSG00000240857 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:18560332..18560642 26863196 MeRIP-seq:(Medium) rs1315766053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244049,Human_RBP_ID_777627,Human_RBP_ID_4622225,Human_RBP_ID_5470279,Human_RBP_ID_5501389 88717 RMVar_ID_88717 Human_SNP_ID_62806708 m1A Human chr2 + 19556057 19556057 19556057 AGCAGAAGAGAGATAGCTCAGCCAGCCCACAGAATTCTGAGAAAGTATACATTATTTTGCTTGAA AGCAGAAGAGAGATAGCTCAGCCAGCCCACAGCATTCTGAGAAAGTATACATTATTTTGCTTGAA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:19556054..19556181 26863196 MeRIP-seq:(Medium) rs139910533 Functional Loss SNV dbSNP153 33..33 33 - - - 88718 RMVar_ID_88718 Human_SNP_ID_62806709 m1A Human chr2 + 19556057 19556057 19556057 AGCAGAAGAGAGATAGCTCAGCCAGCCCACAGAATTCTGAGAAAGTATACATTATTTTGCTTGAA AGCAGAAGAGAGATAGCTCAGCCAGCCCACAGTATTCTGAGAAAGTATACATTATTTTGCTTGAA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:19556054..19556181 26863196 MeRIP-seq:(Medium) rs139910533 Functional Loss SNV dbSNP153 33..33 33 - - - 88719 RMVar_ID_88719 Human_SNP_ID_62892798 m1A Human chr2 - 19898113 19898113 19898113 ATGCTGCATGTTATAGGCTGTGAAGTTTGACAATACCCAAAAGAGAATGAAAGTGGAAATGAGAG ATGCTGCATGTTATAGGCTGTGAAGTTTGACAGTACCCAAAAGAGAATGAAAGTGGAAATGAGAG T C TTC32 Ensembl:ENSG00000183891 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12328613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13734058,Human_RBP_ID_23846720 GWAS_ID_11167,GWAS_ID_11168,GWAS_ID_11169,GWAS_ID_11170,GWAS_ID_11171 88720 RMVar_ID_88720 Human_SNP_ID_62913108 m1A Human chr2 - 19985327 19985317 19985327 TCCTGGGTTGGAGTTGCTGGTGGTAGGGTTTGAGGATGATGGCCCTGGGTTGGAGCTGCTTGTGG TCCTGGGTTGGAGTTGCTGGTGGTAGGGTTTG__________CCCTGGGTTGGAGCTGCTTGTGG GCCATCATCCT G WDR35 Ensembl:ENSG00000118965 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:19985276..19985424 26863196 MeRIP-seq:(Medium) rs879871857 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_827035,Human_RBP_ID_8200404,Human_RBP_ID_13737264,Human_RBP_ID_17136424,Human_RBP_ID_23232356,Human_RBP_ID_26786787,Human_RBP_ID_27691115 88721 RMVar_ID_88721 Human_SNP_ID_62913118 m1A Human chr2 + 19985323 19985323 19985323 CCTACCACAAGCAGCTCCAACCCAGGGCCATCATCCTCAAACCCTACCACCAGCAACTCCAACCC CCTACCACAAGCAGCTCCAACCCAGGGCCATCGTCCTCAAACCCTACCACCAGCAACTCCAACCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:19985239..19985425 26863196 MeRIP-seq:(Medium) rs1451971326 Functional Loss SNV dbSNP153 33..33 33 - - - 88722 RMVar_ID_88722 Human_SNP_ID_62925564 m1A Human chr2 - 20037561 20037561 20037561 CCGTCTCTGTTCTTATGTTTATAATCAGTTCAATGCTGGTTTATGGAGCAATTTCTGTAAGTATA CCGTCTCTGTTCTTATGTTTATAATCAGTTCAGTGCTGGTTTATGGAGCAATTTCTGTAAGTATA T C LAPTM4A Ensembl:ENSG00000068697 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs751339010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542094,Human_RBP_ID_1907559,Human_RBP_ID_22764906,Human_RBP_ID_24487675 Human_Splice_Rec_221206,Human_Splice_Rec_221207 Human_miRNA_ID_2440308 RMVar_hsa_circ_7536,RMVar_hsa_circ_116851,RMVar_hsa_circ_197315,RMVar_hsa_circ_114946,RMVar_hsa_circ_34167,RMVar_hsa_circ_120431,RMVar_hsa_circ_77202,RMVar_hsa_circ_197322,RMVar_hsa_circ_197323,RMVar_hsa_circ_197321 88723 RMVar_ID_88723 Human_SNP_ID_62926435 m1A Human chr2 - 20041009 20040992 20041010 ATGTAACTGATAGAATGTTATCTTTTCCAGGTAGTAAACCTATTGATGGCAATTTTGCTGACTGT ATGTAACTGATAGAATGTTATCTTTTCCAGG__________________CAATTTTGCTGACTGT GCCATCAATAGGTTTACTA G LAPTM4A Ensembl:ENSG00000068697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:20040981..20051579 32194978 MeRIP-seq:(Medium) rs1168193496 Functional Loss DEL dbSNP153 32..49 33 - - - Human_RBP_ID_915306,Human_RBP_ID_22451051,Human_RBP_ID_22667048 Human_Splice_Rec_221204 Human_miRNA_ID_2298148 RMVar_hsa_circ_7536,RMVar_hsa_circ_116851,RMVar_hsa_circ_197315,RMVar_hsa_circ_34167,RMVar_hsa_circ_120431,RMVar_hsa_circ_77202,RMVar_hsa_circ_197322,RMVar_hsa_circ_197323 88724 RMVar_ID_88724 Human_SNP_ID_62926443 m1A Human chr2 - 20041009 20041009 20041009 ATGTAACTGATAGAATGTTATCTTTTCCAGGTAGTAAACCTATTGATGGCAATTTTGCTGACTGT ATGTAACTGATAGAATGTTATCTTTTCCAGGTGGTAAACCTATTGATGGCAATTTTGCTGACTGT T C LAPTM4A Ensembl:ENSG00000068697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:20040981..20051579 32194978 MeRIP-seq:(Medium) rs141893598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915306,Human_RBP_ID_22451051,Human_RBP_ID_22667048 Human_Splice_Rec_221204 Human_miRNA_ID_2298148 RMVar_hsa_circ_7536,RMVar_hsa_circ_116851,RMVar_hsa_circ_197315,RMVar_hsa_circ_34167,RMVar_hsa_circ_120431,RMVar_hsa_circ_77202,RMVar_hsa_circ_197322,RMVar_hsa_circ_197323 88725 RMVar_ID_88725 Human_SNP_ID_62929211 m1A Human chr2 + 20051576 20051576 20051576 GGCCGGGCCCCTGACAAACGTTCTCCACCCGCAGCCAAACTCAAACGGCTGTTTCACGGCCTCCA GGCCGGGCCCCTGACAAACGTTCTCCACCCGCTGCCAAACTCAAACGGCTGTTTCACGGCCTCCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:20051551..20051575 26863196 MeRIP-seq:(Medium) rs11542926 Functional Loss SNV dbSNP153 33..33 33 - - - 88726 RMVar_ID_88726 Human_SNP_ID_62929224 m1A Human chr2 + 20051610 20051610 20051610 CCAAACTCAAACGGCTGTTTCACGGCCTCCAAAACCCAACGACGCGTCTTCAAACCCGCCCCCGG CCAAACTCAAACGGCTGTTTCACGGCCTCCAACACCCAACGACGCGTCTTCAAACCCGCCCCCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:20051462..20051693;chr2:20051481..20051700 26863196 MeRIP-seq:(Medium) rs547935294 Functional Loss SNV dbSNP153 33..33 33 - - - 88727 RMVar_ID_88727 Human_SNP_ID_62956859 m1A Human chr2 + 20165126 20165126 20165126 CTCACCACACTCACCACACATACCACACTCACACCACACACATACCACATACCACACTCACCCCA CTCACCACACTCACCACACATACCACACTCACCCCACACACATACCACATACCACACTCACCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:20165105..20165170 26863196 MeRIP-seq:(Medium) rs532998720 Functional Loss SNV dbSNP153 33..33 33 - - - 88728 RMVar_ID_88728 Human_SNP_ID_62966527 m1A Human chr2 - 20202694 20202694 20202694 GGCCCCCACTTGCCTCTTCCTTGAAGAACTGCAGGCCCTGGCCTCCCCTGCCACCAGGCCACCTC GGCCCCCACTTGCCTCTTCCTTGAAGAACTGCGGGCCCTGGCCTCCCCTGCCACCAGGCCACCTC T C SDC1 Ensembl:ENSG00000115884 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:20202596..20202733 26863196 MeRIP-seq:(Medium) rs892910432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143043,Human_RBP_ID_4593084,Human_RBP_ID_17658378,Human_RBP_ID_22450167,Human_RBP_ID_27477025 Human_miRNA_ID_2572029,Human_miRNA_ID_2572030 RMVar_hsa_circ_77137,RMVar_hsa_circ_94838,RMVar_hsa_circ_119343,RMVar_hsa_circ_103727,RMVar_hsa_circ_87107,RMVar_hsa_circ_94157,RMVar_hsa_circ_82705,RMVar_hsa_circ_197328,RMVar_hsa_circ_197330,RMVar_hsa_circ_197332,RMVar_hsa_circ_197333,RMVar_hsa_circ_197331,RMVar_hsa_circ_197329,RMVar_hsa_circ_197327 88729 RMVar_ID_88729 Human_SNP_ID_62966541 m1A Human chr2 - 20202730 20202730 20202730 GGGAGCCATGCGCCCCCTCCGCCCTGCCACTCACTAGGCCCCCACTTGCCTCTTCCTTGAAGAAC GGGAGCCATGCGCCCCCTCCGCCCTGCCACTCTCTAGGCCCCCACTTGCCTCTTCCTTGAAGAAC T A SDC1 Ensembl:ENSG00000115884 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:20202679..20202882 26863196 MeRIP-seq:(Medium) rs1558429011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143043,Human_RBP_ID_26479084 Human_miRNA_ID_2382165,Human_miRNA_ID_2382166 RMVar_hsa_circ_77137,RMVar_hsa_circ_94838,RMVar_hsa_circ_119343,RMVar_hsa_circ_103727,RMVar_hsa_circ_87107,RMVar_hsa_circ_94157,RMVar_hsa_circ_82705,RMVar_hsa_circ_197328,RMVar_hsa_circ_197330,RMVar_hsa_circ_197332,RMVar_hsa_circ_197333,RMVar_hsa_circ_197331,RMVar_hsa_circ_197329,RMVar_hsa_circ_197327 88730 RMVar_ID_88730 Human_SNP_ID_63030392 m1A Human chr2 + 20447129 20447119 20447129 AGCTGTTGTCTTGTATGCTCAGCGAGGCCCGGAGAGACCCGGGAGAGAGCTAGGCCGAGTCCACC AGCTGTTGTCTTGTATGCTCAGC__________GAGACCCGGGAGAGAGCTAGGCCGAGTCCACC CGAGGCCCGGA C RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:20447076..20447350 26863196 MeRIP-seq:(Medium) rs1558280602 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_542826,Human_RBP_ID_1582621,Human_RBP_ID_4624065,Human_RBP_ID_5147024,Human_RBP_ID_5528376,Human_RBP_ID_22451064 88731 RMVar_ID_88731 Human_SNP_ID_63030398 m1A Human chr2 + 20447129 20447129 20447129 AGCTGTTGTCTTGTATGCTCAGCGAGGCCCGGAGAGACCCGGGAGAGAGCTAGGCCGAGTCCACC AGCTGTTGTCTTGTATGCTCAGCGAGGCCCGGGGAGACCCGGGAGAGAGCTAGGCCGAGTCCACC A G RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:20447076..20447350 26863196 MeRIP-seq:(Medium) rs1236259601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542826,Human_RBP_ID_1582621,Human_RBP_ID_4624065,Human_RBP_ID_5147024,Human_RBP_ID_5528376,Human_RBP_ID_22451064 88732 RMVar_ID_88732 Human_SNP_ID_63030443 m1A Human chr2 + 20447206 20447206 20447206 TGCCCGAGCCCGCGTTACGCACAAAGCCGCCGATCCCCGGCCTGGGGTGAGCAGAGCGACCACCG TGCCCGAGCCCGCGTTACGCACAAAGCCGCCGGTCCCCGGCCTGGGGTGAGCAGAGCGACCACCG A G RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr2:20447076..20447500;chr2:20447076..20447575 26863196,26863410 MeRIP-seq:(Medium) rs1398309181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777123,Human_RBP_ID_4624066,Human_RBP_ID_18470970,Human_RBP_ID_22451064,Human_RBP_ID_23849847 88733 RMVar_ID_88733 Human_SNP_ID_63030459 m1A Human chr2 + 20447245 20447245 20447245 GCCTGGGGTGAGCAGAGCGACCACCGCCCGGGAGCAGCGCGGCGAGACGCACGGTGCGCCCTATG GCCTGGGGTGAGCAGAGCGACCACCGCCCGGGGGCAGCGCGGCGAGACGCACGGTGCGCCCTATG A G RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:20447148..20447285 26863196 MeRIP-seq:(Medium) rs1423633961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542827,Human_RBP_ID_777123,Human_RBP_ID_4622240,Human_RBP_ID_22451064,Human_RBP_ID_27285917 88734 RMVar_ID_88734 Human_SNP_ID_63030460 m1A Human chr2 + 20447248 20447248 20447248 TGGGGTGAGCAGAGCGACCACCGCCCGGGAGCAGCGCGGCGAGACGCACGGTGCGCCCTATGCCC TGGGGTGAGCAGAGCGACCACCGCCCGGGAGCGGCGCGGCGAGACGCACGGTGCGCCCTATGCCC A G RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:20447146..20447256 26863410 MeRIP-seq:(Medium) rs1221417456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542827,Human_RBP_ID_777123,Human_RBP_ID_4593587,Human_RBP_ID_22451064 88735 RMVar_ID_88735 Human_SNP_ID_63030513 m1A Human chr2 + 20447372 20447372 20447372 GGGGCCCGGGTGCAGCTAGCGACCCTCTCGCCACCTGCGCGCAGCCCGAGGTGAGCAGTGAGCGG GGGGCCCGGGTGCAGCTAGCGACCCTCTCGCCCCCTGCGCGCAGCCCGAGGTGAGCAGTGAGCGG A C RHOB Ensembl:ENSG00000143878 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:20447271..20447420 26863410 MeRIP-seq:(Medium) rs557972851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622241,Human_RBP_ID_22450179 88736 RMVar_ID_88736 Human_SNP_ID_63030630 m1A Human chr2 + 20447665 20447665 20447665 GCTGTGGGACACGGCGGGCCAGGAGGACTACGACCGCCTGCGGCCGCTCTCCTACCCGGACACCG GCTGTGGGACACGGCGGGCCAGGAGGACTACGCCCGCCTGCGGCCGCTCTCCTACCCGGACACCG A C RHOB Ensembl:ENSG00000143878 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:20447616..20447815 32194978 MeRIP-seq:(Medium) rs201421541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4629690,Human_RBP_ID_5147025,Human_RBP_ID_6878240,Human_RBP_ID_27285924,Human_RBP_ID_27477117 88737 RMVar_ID_88737 Human_SNP_ID_63030737 m1A Human chr2 + 20447952 20447952 20447952 AAGCCTACGACTACCTCGAGTGCTCTGCCAAGACCAAGGAAGGCGTGCGCGAGGTCTTCGAGACG AAGCCTACGACTACCTCGAGTGCTCTGCCAAGTCCAAGGAAGGCGTGCGCGAGGTCTTCGAGACG A T RHOB Ensembl:ENSG00000143878 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:20447901..20448000 32194978 MeRIP-seq:(Medium) rs1311239411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6878243,Human_RBP_ID_13751367,Human_RBP_ID_22247240,Human_RBP_ID_27006181,Human_RBP_ID_27285928 88738 RMVar_ID_88738 Human_SNP_ID_63030789 m1A Human chr2 - 20448069 20448069 20448069 GAGGGGGAGCCGTGCCGGCAGGGGCAGGCGCGACGGGCGCGGCCCTCATAGCACCTTGCAGCAGT GAGGGGGAGCCGTGCCGGCAGGGGCAGGCGCGGCGGGCGCGGCCCTCATAGCACCTTGCAGCAGT T C lnc-PUM2-1 RNACentral:URS0000D58E77 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:20447926..20448250 26863410 MeRIP-seq:(Medium) rs1465534024 Functional Loss SNV dbSNP153 33..33 33 - - - 88739 RMVar_ID_88739 Human_SNP_ID_63030820 m1A Human chr2 + 20448106 20448106 20448106 CCTGCCCCTGCCGGCACGGCTCCCCCTCCTGGACCAGTCCCCCGCGAGCCCGGAGAAGGGGAGAC CCTGCCCCTGCCGGCACGGCTCCCCCTCCTGGGCCAGTCCCCCGCGAGCCCGGAGAAGGGGAGAC A G RHOB Ensembl:ENSG00000143878 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:20448036..20448185 26863196 MeRIP-seq:(Medium) rs748602850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243737,Human_RBP_ID_542834,Human_RBP_ID_8201991,Human_RBP_ID_17948665,Human_RBP_ID_22077490,Human_RBP_ID_22450181,Human_RBP_ID_23849853,Human_RBP_ID_27006183,Human_RBP_ID_27285930,Human_RBP_ID_27477136,Human_RBP_ID_27563467 88740 RMVar_ID_88740 Human_SNP_ID_63031023 m1A Human chr2 + 20448667 20448667 20448667 GACTCCCGCCCAAGCATGAACAGGACTTGACCATCTTTCCAACCCCTGGGGAAGACATTTGCAAC GACTCCCGCCCAAGCATGAACAGGACTTGACCTTCTTTCCAACCCCTGGGGAAGACATTTGCAAC A T RHOB Ensembl:ENSG00000143878 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:20448616..20448823 26863196 MeRIP-seq:(Medium) rs902481703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_542852,Human_RBP_ID_4629713,Human_RBP_ID_5147027,Human_RBP_ID_6878265,Human_RBP_ID_8845084,Human_RBP_ID_13751372,Human_RBP_ID_18313862,Human_RBP_ID_22247252,Human_RBP_ID_23849874,Human_RBP_ID_26479192,Human_RBP_ID_27285942,Human_RBP_ID_27477172,Human_RBP_ID_27563472 88741 RMVar_ID_88741 Human_SNP_ID_63075492 m1A Human chr2 + 20619099 20619099 20619099 GGATCTGCTCCTGCGGCTTCTGCTGCCCAGCCACAGCTTCAGCCGGGCCCGCTTTGGGGGGAACA GGATCTGCTCCTGCGGCTTCTGCTGCCCAGCCTCAGCTTCAGCCGGGCCCGCTTTGGGGGGAACA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:20619048..20619125 26863196 MeRIP-seq:(Medium) rs756522204 Functional Loss SNV dbSNP153 33..33 33 - - - 88742 RMVar_ID_88742 Human_SNP_ID_63765075 m1A Human chr2 - 23379468 23379460 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT________CCCCCCCCCCCCCCGCCCCACAGCT GGGGGGGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1420600749 Functional Loss DEL dbSNP153 33..40 33 - - - 88743 RMVar_ID_88743 Human_SNP_ID_63765079 m1A Human chr2 - 23379468 23379461 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT_______CCCCCCCCCCCCCCCGCCCCACAGCT GGGGGGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1206794236 Functional Loss DEL dbSNP153 33..39 33 - - - 88744 RMVar_ID_88744 Human_SNP_ID_63765083 m1A Human chr2 - 23379468 23379462 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT______CCCCCCCCCCCCCCCCGCCCCACAGCT GGGGGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1194950293 Functional Loss DEL dbSNP153 33..38 33 - - - 88745 RMVar_ID_88745 Human_SNP_ID_63765086 m1A Human chr2 - 23379468 23379463 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT_____CCCCCCCCCCCCCCCCCGCCCCACAGCT GGGGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1233801610 Functional Loss DEL dbSNP153 33..37 33 - - - 88746 RMVar_ID_88746 Human_SNP_ID_63765089 m1A Human chr2 - 23379468 23379464 23379469 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCG_____CCCCCCCCCCCCCCCCCCGCCCCACAGCT GGGGTA G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1327804368 Functional Loss DEL dbSNP153 32..36 33 - - - 88747 RMVar_ID_88747 Human_SNP_ID_63765090 m1A Human chr2 - 23379468 23379464 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT____CCCCCCCCCCCCCCCCCCGCCCCACAGCT GGGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1354685929 Functional Loss DEL dbSNP153 33..36 33 - - - 88748 RMVar_ID_88748 Human_SNP_ID_63765095 m1A Human chr2 - 23379468 23379465 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGT___CCCCCCCCCCCCCCCCCCCGCCCCACAGCT GGGT G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1558316062 Functional Loss DEL dbSNP153 33..35 33 - - - 88749 RMVar_ID_88749 Human_SNP_ID_63765105 m1A Human chr2 - 23379468 23379468 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGTTCCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT T A AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1163107851 Functional Loss SNV dbSNP153 33..33 33 - - - 88750 RMVar_ID_88750 Human_SNP_ID_63765106 m1A Human chr2 - 23379468 23379468 23379468 GCTCTGTCTCAGGTGTTACTGGTAATCACCGTACCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT GCTCTGTCTCAGGTGTTACTGGTAATCACCGTCCCCCCCCCCCCCCCCCCCCCCGCCCCACAGCT T G AC012506.4 Ensembl:ENSG00000235497 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23379426..23379475 26863196 MeRIP-seq:(Medium) rs1163107851 Functional Loss SNV dbSNP153 33..33 33 - - - 88751 RMVar_ID_88751 Human_SNP_ID_63766724 m1A Human chr2 + 23385240 23385240 23385240 AGGGAGCATGGTCCCCGCGCCGCGGCCGCGCCAGCCCCCGCGCCGCCGCCGCCGTCCCCGCCACC AGGGAGCATGGTCCCCGCGCCGCGGCCGCGCCGGCCCCCGCGCCGCCGCCGCCGTCCCCGCCACC A G KLHL29 Ensembl:ENSG00000119771 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:23385201..23385790;chr2:23385203..23385357 26863196 MeRIP-seq:(Medium) rs979812017 Functional Loss SNV dbSNP153 33..33 33 - - - 88752 RMVar_ID_88752 Human_SNP_ID_63766759 m1A Human chr2 - 23385308 23385302 23385308 GCGACCGCCGGGGCTGCGGACGGGCGCTGCGGAGCCGGGGCCGGGGCTGGAGCTGCGGCGAGATC GCGACCGCCGGGGCTGCGGACGGGCGCTGCGG______GGCCGGGGCTGGAGCTGCGGCGAGATC CCCGGCT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:23385176..23385400 26863410 MeRIP-seq:(Medium) rs923359542 Functional Loss DEL dbSNP153 33..38 33 - - - 88753 RMVar_ID_88753 Human_SNP_ID_63766761 m1A Human chr2 - 23385308 23385308 23385308 GCGACCGCCGGGGCTGCGGACGGGCGCTGCGGAGCCGGGGCCGGGGCTGGAGCTGCGGCGAGATC GCGACCGCCGGGGCTGCGGACGGGCGCTGCGGGGCCGGGGCCGGGGCTGGAGCTGCGGCGAGATC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:23385176..23385400 26863410 MeRIP-seq:(Medium) rs1468132964 Functional Loss SNV dbSNP153 33..33 33 - - - 88754 RMVar_ID_88754 Human_SNP_ID_63766846 m1A Human chr2 - 23385537 23385537 23385537 CGCCTCCCGGCAGCCCAGGGAGGATGCCCGGGAGAGGGAAGTCGGTCCTCCTGCCTGTCAGCCTG CGCCTCCCGGCAGCCCAGGGAGGATGCCCGGGGGAGGGAAGTCGGTCCTCCTGCCTGTCAGCCTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:23385526..23385750 26863196 MeRIP-seq:(Medium) rs1300347710 Functional Loss SNV dbSNP153 33..33 33 - - - 88755 RMVar_ID_88755 Human_SNP_ID_63766879 m1A Human chr2 + 23385624 23385622 23385625 AACGAGGGGAGAAGGCGGAGAGCAGGAACGCGAGGAGGAGGACCTGGATCCGTTTCCTCCGGCCA AACGAGGGGAGAAGGCGGAGAGCAGGAACGC___GAGGAGGACCTGGATCCGTTTCCTCCGGCCA CGAG C KLHL29 Ensembl:ENSG00000119771 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:23385418..23385770;chr2:23385176..23385825 26863196 MeRIP-seq:(Medium) rs1037918759 Functional Loss DEL dbSNP153 32..34 33 - - - 88756 RMVar_ID_88756 Human_SNP_ID_63766884 m1A Human chr2 - 23385636 23385636 23385636 CCGCTCGGGTCCTGGCCGGAGGAAACGGATCCAGGTCCTCCTCCTCGCGTTCCTGCTCTCCGCCT CCGCTCGGGTCCTGGCCGGAGGAAACGGATCCGGGTCCTCCTCCTCGCGTTCCTGCTCTCCGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:23385530..23385637 32194978 MeRIP-seq:(Medium) rs1216923859 Functional Loss SNV dbSNP153 33..33 33 - - - 88757 RMVar_ID_88757 Human_SNP_ID_63767183 m1A Human chr2 - 23386446 23386446 23386446 CAACACGCTGGCACCCACAAGGTGTCAAGGGAAGTGTGCGTGTGTGTGTCGGGGTGGGGTGGGTC CAACACGCTGGCACCCACAAGGTGTCAAGGGACGTGTGCGTGTGTGTGTCGGGGTGGGGTGGGTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23386442..23386906 26863196 MeRIP-seq:(Medium) rs898337336 Functional Loss SNV dbSNP153 33..33 33 - - - 88758 RMVar_ID_88758 Human_SNP_ID_63767213 m1A Human chr2 - 23386530 23386530 23386530 CCACACATCAACAACCCCTCCCCAACGACACCACCTCCTGGCCGCTTCGCCGTCCCCGTGAGCTC CCACACATCAACAACCCCTCCCCAACGACACCGCCTCCTGGCCGCTTCGCCGTCCCCGTGAGCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:23386479..23386923 26863196 MeRIP-seq:(Medium) rs1199859478 Functional Loss SNV dbSNP153 33..33 33 - - - 88759 RMVar_ID_88759 Human_SNP_ID_63767332 m1A Human chr2 - 23387001 23387001 23387001 CTTACCCATCAGCATCTCTGGGGGCCCGCGCGAGGGCCCGCCAACGGACCGCGTCTGCCGCTTGG CTTACCCATCAGCATCTCTGGGGGCCCGCGCGGGGGCCCGCCAACGGACCGCGTCTGCCGCTTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23386997..23387128 26863196 MeRIP-seq:(Medium) rs919868342 Functional Loss SNV dbSNP153 33..33 33 - - - 88760 RMVar_ID_88760 Human_SNP_ID_63773534 m1A Human chr2 - 23410369 23410369 23410369 TCCATCCAGTAATCTAGGGGTCACCTTGAGACATCCCTCTCCTTTACTTCCCACCCTCGAACCCC TCCATCCAGTAATCTAGGGGTCACCTTGAGACGTCCCTCTCCTTTACTTCCCACCCTCGAACCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23410366..23410508 26863196 MeRIP-seq:(Medium) rs891343008 Functional Loss SNV dbSNP153 33..33 33 - - - 88761 RMVar_ID_88761 Human_SNP_ID_63773707 m1A Human chr2 - 23411150 23411150 23411150 GATTTGGACATCCCTATATTTCAACATTTGTCATATCGACATTATAACCCCATCTTGTGCCTCCA GATTTGGACATCCCTATATTTCAACATTTGTCGTATCGACATTATAACCCCATCTTGTGCCTCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23411144..23411529 26863196 MeRIP-seq:(Medium) rs1256046216 Functional Loss SNV dbSNP153 33..33 33 - - - 88762 RMVar_ID_88762 Human_SNP_ID_63773725 m1A Human chr2 - 23411240 23411240 23411240 ACCCTGTCCTCAACCTTTGCTACATGTCACAAATCCCTAGGCCTTCTCTCACTCCCTTGAACTGC ACCCTGTCCTCAACCTTTGCTACATGTCACAAGTCCCTAGGCCTTCTCTCACTCCCTTGAACTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:23411235..23411450 26863196 MeRIP-seq:(Medium) rs1308051125 Functional Loss SNV dbSNP153 33..33 33 - - - 88763 RMVar_ID_88763 Human_SNP_ID_63776612 m1A Human chr2 - 23421958 23421955 23421959 ACACATGAACACACACACAACATATGACACACACAGACACACAAAGGCAGACACACTGACTCAGA ACACATGAACACACACACAACATATGACACA____GACACACAAAGGCAGACACACTGACTCAGA CTGTG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:23421908..23422068 26863196 MeRIP-seq:(Medium) rs556842507 Functional Loss DEL dbSNP153 32..35 33 - - - 88764 RMVar_ID_88764 Human_SNP_ID_63776613 m1A Human chr2 - 23421958 23421955 23421959 ACACATGAACACACACACAACATATGACACACACAGACACACAAAGGCAGACACACTGACTCAGA ACACATGAACACACACACAACATATGACACA__CAGACACACAAAGGCAGACACACTGACTCAGA CTGTG CTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:23421908..23422068 26863196 MeRIP-seq:(Medium) rs556842507 Functional Loss DEL dbSNP153 32..33 33 - - - 88765 RMVar_ID_88765 Human_SNP_ID_63776678 m1A Human chr2 - 23422117 23422117 23422117 CACAGACACACACAACACACAAAGACCCACCCATACTGACACACTCACACAAACATACAGACAGC CACAGACACACACAACACACAAAGACCCACCCTTACTGACACACTCACACAAACATACAGACAGC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:23422093..23422222 26863196 MeRIP-seq:(Medium) rs948699054 Functional Loss SNV dbSNP153 33..33 33 - - - 88766 RMVar_ID_88766 Human_SNP_ID_63776764 m1A Human chr2 - 23422376 23422376 23422376 ACACATAGGCATATGAAAATACAGAGACACACACAGACACACACACACAAACACAACACACAAAG ACACATAGGCATATGAAAATACAGAGACACACGCAGACACACACACACAAACACAACACACAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23422370..23422704 26863196 MeRIP-seq:(Medium) rs1241227072 Functional Loss SNV dbSNP153 33..33 33 - - - 88767 RMVar_ID_88767 Human_SNP_ID_63776837 m1A Human chr2 - 23422605 23422605 23422605 ACACAGACACAGACAGGGACACACACACAGGCACACAACACAGAGACACAGACACACAGACAGGG ACACAGACACAGACAGGGACACACACACAGGCGCACAACACAGAGACACAGACACACAGACAGGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:23422400..23422725 26863196 MeRIP-seq:(Medium) rs1052711149 Functional Loss SNV dbSNP153 33..33 33 - - - 88768 RMVar_ID_88768 Human_SNP_ID_63786607 m1A Human chr2 + 23460639 23460639 23460639 CAGTGGAGCTGGCCAAGCAGAAGATGAGGGACAGACAAGACAGGTGGAGGCCACAGGTGTGGAAA CAGTGGAGCTGGCCAAGCAGAAGATGAGGGACCGACAAGACAGGTGGAGGCCACAGGTGTGGAAA A C KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23460634..23460700 26863196 MeRIP-seq:(Medium) rs1052621614 Functional Loss SNV dbSNP153 33..33 33 - - - 88769 RMVar_ID_88769 Human_SNP_ID_63786608 m1A Human chr2 + 23460639 23460639 23460639 CAGTGGAGCTGGCCAAGCAGAAGATGAGGGACAGACAAGACAGGTGGAGGCCACAGGTGTGGAAA CAGTGGAGCTGGCCAAGCAGAAGATGAGGGACGGACAAGACAGGTGGAGGCCACAGGTGTGGAAA A G KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23460634..23460700 26863196 MeRIP-seq:(Medium) rs1052621614 Functional Loss SNV dbSNP153 33..33 33 - - - 88770 RMVar_ID_88770 Human_SNP_ID_63793350 m1A Human chr2 + 23487086 23487086 23487086 CTAGAAAGCCCAGGTCTGGAGTTCACATCTGTATGATGTGAGAGCTCTCACTCTTAGCCAGGGTG CTAGAAAGCCCAGGTCTGGAGTTCACATCTGTGTGATGTGAGAGCTCTCACTCTTAGCCAGGGTG A G KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:23487035..23487165 26863196 MeRIP-seq:(Medium) rs1035877531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197465,RMVar_hsa_circ_283802,RMVar_hsa_circ_197464 88771 RMVar_ID_88771 Human_SNP_ID_63803272 m1A Human chr2 + 23526299 23526299 23526299 GCGGTCGGAGGAAGCGTCACAGGGGAGGGGAAACCAGAGCTGTGGTCAGGGCATGCGGGAGGGGT GCGGTCGGAGGAAGCGTCACAGGGGAGGGGAATCCAGAGCTGTGGTCAGGGCATGCGGGAGGGGT A T KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23526293..23526521 26863196 MeRIP-seq:(Medium) rs561227097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197465,RMVar_hsa_circ_283802 88772 RMVar_ID_88772 Human_SNP_ID_63803277 m1A Human chr2 + 23526319 23526319 23526319 AGGGGAGGGGAAACCAGAGCTGTGGTCAGGGCATGCGGGAGGGGTGGCATCGAAGGCAGAGGGAC AGGGGAGGGGAAACCAGAGCTGTGGTCAGGGCTTGCGGGAGGGGTGGCATCGAAGGCAGAGGGAC A T KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:23526287..23526390 26863196 MeRIP-seq:(Medium) rs1558373638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197465,RMVar_hsa_circ_283802 88773 RMVar_ID_88773 Human_SNP_ID_63830536 m1A Human chr2 + 23629849 23629849 23629849 AAAATCATTAAGAAAGAAGACAGGGCCCCAACAATCCTGAGAGAGGGAGAGAGAGGCCTGGCACG AAAATCATTAAGAAAGAAGACAGGGCCCCAACGATCCTGAGAGAGGGAGAGAGAGGCCTGGCACG A G KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23629844..23630241 26863196 MeRIP-seq:(Medium) rs939302520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33854 88774 RMVar_ID_88774 Human_SNP_ID_63833874 m1A Human chr2 + 23642602 23642602 23642602 CATGCCTGCCCAGGCCCTGTATGCCAGCCCTCAGCCCCTGGCCGTGTCCACACTGCCCGGTGTGG CATGCCTGCCCAGGCCCTGTATGCCAGCCCTCCGCCCCTGGCCGTGTCCACACTGCCCGGTGTGG A C KLHL29 Ensembl:ENSG00000119771 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:23642551..23642654 26863196 MeRIP-seq:(Medium) rs1206637815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33854,RMVar_hsa_circ_354014 88775 RMVar_ID_88775 Human_SNP_ID_63843852 m1A Human chr2 - 23679860 23679860 23679860 TTCCCTCCCCTTCCTCCATCTGGCCAAGCAGTATTTATCCTTCACCACCAGGGAAAGTGTTATTT TTCCCTCCCCTTCCTCCATCTGGCCAAGCAGTGTTTATCCTTCACCACCAGGGAAAGTGTTATTT T C AC009242.1 Ensembl:ENSG00000283031 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23679853..23680070 26863196 MeRIP-seq:(Medium) rs1052406715 Functional Loss SNV dbSNP153 33..33 33 - - - 88776 RMVar_ID_88776 Human_SNP_ID_63845898 m1A Human chr2 - 23687784 23687784 23687784 CCACCCTCATACCCGGCCCTGCAGCAACGTGGAGTCACCTGTGGGACCTGAGACCCCCTCCCGCC CCACCCTCATACCCGGCCCTGCAGCAACGTGGGGTCACCTGTGGGACCTGAGACCCCCTCCCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23687582..23688001 26863196 MeRIP-seq:(Medium) rs1435621542 Functional Loss SNV dbSNP153 33..33 33 - - - 88777 RMVar_ID_88777 Human_SNP_ID_63863124 m1A Human chr2 + 23757932 23757932 23757932 CCAGTCTCTTCTCCATTTTCCTCATGGCAGTCAGTGCTTACCTCAAACTCTCCATTCTCTAATAA CCAGTCTCTTCTCCATTTTCCTCATGGCAGTCGGTGCTTACCTCAAACTCTCCATTCTCTAATAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23757833..23758046 26863196 MeRIP-seq:(Medium) rs777386586 Functional Loss SNV dbSNP153 33..33 33 - - - 88778 RMVar_ID_88778 Human_SNP_ID_63865273 m1A Human chr2 - 23767211 23767183 23767211 GCGGGAAAAATGGTTATGACAGAGCAGGTAATAGGAATGAGTTAGGGTGGAGTAGGTAATCGGAA GCGGGAAAAATGGTTATGACAGAGCAGGTAAT____________________________CGGAA GATTACCTACTCCACCCTAACTCATTCCT G ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23767175..23767277 26863196 MeRIP-seq:(Medium) rs1558502822 Functional Loss DEL dbSNP153 33..60 33 - - - RMVar_hsa_circ_101569,RMVar_hsa_circ_197471,RMVar_hsa_circ_197470,RMVar_hsa_circ_287028,RMVar_hsa_circ_339938,RMVar_hsa_circ_197472,RMVar_hsa_circ_378245,RMVar_hsa_circ_318633,RMVar_hsa_circ_330779,RMVar_hsa_circ_295635,RMVar_hsa_circ_68399,RMVar_hsa_circ_197475,RMVar_hsa_circ_17289,RMVar_hsa_circ_197474,RMVar_hsa_circ_291166,RMVar_hsa_circ_31288,RMVar_hsa_circ_67907,RMVar_hsa_circ_320286,RMVar_hsa_circ_346741,RMVar_hsa_circ_357060,RMVar_hsa_circ_317134,RMVar_hsa_circ_70817,RMVar_hsa_circ_106535,RMVar_hsa_circ_66205,RMVar_hsa_circ_25148,RMVar_hsa_circ_197477,RMVar_hsa_circ_197478,RMVar_hsa_circ_197479,RMVar_hsa_circ_197476 88779 RMVar_ID_88779 Human_SNP_ID_63865284 m1A Human chr2 - 23767211 23767211 23767211 GCGGGAAAAATGGTTATGACAGAGCAGGTAATAGGAATGAGTTAGGGTGGAGTAGGTAATCGGAA GCGGGAAAAATGGTTATGACAGAGCAGGTAATCGGAATGAGTTAGGGTGGAGTAGGTAATCGGAA T G ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23767175..23767277 26863196 MeRIP-seq:(Medium) rs1384854836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101569,RMVar_hsa_circ_197471,RMVar_hsa_circ_197470,RMVar_hsa_circ_287028,RMVar_hsa_circ_339938,RMVar_hsa_circ_197472,RMVar_hsa_circ_378245,RMVar_hsa_circ_318633,RMVar_hsa_circ_330779,RMVar_hsa_circ_295635,RMVar_hsa_circ_68399,RMVar_hsa_circ_197475,RMVar_hsa_circ_17289,RMVar_hsa_circ_197474,RMVar_hsa_circ_291166,RMVar_hsa_circ_31288,RMVar_hsa_circ_67907,RMVar_hsa_circ_320286,RMVar_hsa_circ_346741,RMVar_hsa_circ_357060,RMVar_hsa_circ_317134,RMVar_hsa_circ_70817,RMVar_hsa_circ_106535,RMVar_hsa_circ_66205,RMVar_hsa_circ_25148,RMVar_hsa_circ_197477,RMVar_hsa_circ_197478,RMVar_hsa_circ_197479,RMVar_hsa_circ_197476 88780 RMVar_ID_88780 Human_SNP_ID_63890433 m1A Human chr2 - 23871214 23871214 23871214 TAAGCGAAACCTAGGTAGGGGTGGAGAAGAAGACGATATAAGGGATATTTACAGGGAATGTGGCT TAAGCGAAACCTAGGTAGGGGTGGAGAAGAAGTCGATATAAGGGATATTTACAGGGAATGTGGCT T A ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23871204..23871320 26863196 MeRIP-seq:(Medium) rs1558697634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_750,RMVar_hsa_circ_330779,RMVar_hsa_circ_364574,RMVar_hsa_circ_316297,RMVar_hsa_circ_124269,RMVar_hsa_circ_295520,RMVar_hsa_circ_317866,RMVar_hsa_circ_74695,RMVar_hsa_circ_47341,RMVar_hsa_circ_197489,RMVar_hsa_circ_197490,RMVar_hsa_circ_33627,RMVar_hsa_circ_54161,RMVar_hsa_circ_88894,RMVar_hsa_circ_79389,RMVar_hsa_circ_197515,RMVar_hsa_circ_197516,RMVar_hsa_circ_197519,RMVar_hsa_circ_273072,RMVar_hsa_circ_340077,RMVar_hsa_circ_370511,RMVar_hsa_circ_309152,RMVar_hsa_circ_302561,RMVar_hsa_circ_281740,RMVar_hsa_circ_197521,RMVar_hsa_circ_197522,RMVar_hsa_circ_197520,RMVar_hsa_circ_13830,RMVar_hsa_circ_197518,RMVar_hsa_circ_369103,RMVar_hsa_circ_302288,RMVar_hsa_circ_284658,RMVar_hsa_circ_197525,RMVar_hsa_circ_197526,RMVar_hsa_circ_197528,RMVar_hsa_circ_285179,RMVar_hsa_circ_346006,RMVar_hsa_circ_26423,RMVar_hsa_circ_306555,RMVar_hsa_circ_285299,RMVar_hsa_circ_37504,RMVar_hsa_circ_73524,RMVar_hsa_circ_197529,RMVar_hsa_circ_197527 88781 RMVar_ID_88781 Human_SNP_ID_63893018 m1A Human chr2 - 23880722 23880722 23880722 ATCTCAAGAGGAGGATGGAGATATAGAAGTTGAAGAGGCAGAAGGAGAAGAAAATGATAGACCAT ATCTCAAGAGGAGGATGGAGATATAGAAGTTGGAGAGGCAGAAGGAGAAGAAAATGATAGACCAT T C ATAD2B Ensembl:ENSG00000119778 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:23880671..23880798 26863196 MeRIP-seq:(Medium) rs764561771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9192,Human_RBP_ID_58370,Human_RBP_ID_829781,Human_RBP_ID_916179,Human_RBP_ID_9383255,Human_RBP_ID_22417046,Human_RBP_ID_24545765,Human_RBP_ID_26339037,Human_RBP_ID_27816847 Human_Splice_Rec_222226,Human_Splice_Rec_222227,Human_Splice_Rec_222360,Human_Splice_Rec_222361 RMVar_hsa_circ_750,RMVar_hsa_circ_330779,RMVar_hsa_circ_364574,RMVar_hsa_circ_316297,RMVar_hsa_circ_124269,RMVar_hsa_circ_295520,RMVar_hsa_circ_317866,RMVar_hsa_circ_47341,RMVar_hsa_circ_197489,RMVar_hsa_circ_197490,RMVar_hsa_circ_33627,RMVar_hsa_circ_54161,RMVar_hsa_circ_88894,RMVar_hsa_circ_79389,RMVar_hsa_circ_197515,RMVar_hsa_circ_197516,RMVar_hsa_circ_197519,RMVar_hsa_circ_273072,RMVar_hsa_circ_370511,RMVar_hsa_circ_309152,RMVar_hsa_circ_302561,RMVar_hsa_circ_281740,RMVar_hsa_circ_197521,RMVar_hsa_circ_197520,RMVar_hsa_circ_13830,RMVar_hsa_circ_197518,RMVar_hsa_circ_302288,RMVar_hsa_circ_284658,RMVar_hsa_circ_197525,RMVar_hsa_circ_197526,RMVar_hsa_circ_197535,RMVar_hsa_circ_197528,RMVar_hsa_circ_285179,RMVar_hsa_circ_346006,RMVar_hsa_circ_26423,RMVar_hsa_circ_285299,RMVar_hsa_circ_37504,RMVar_hsa_circ_73524,RMVar_hsa_circ_197532,RMVar_hsa_circ_272148,RMVar_hsa_circ_280436,RMVar_hsa_circ_197527,RMVar_hsa_circ_311936,RMVar_hsa_circ_278436,RMVar_hsa_circ_197533,RMVar_hsa_circ_197537,RMVar_hsa_circ_302562,RMVar_hsa_circ_319069,RMVar_hsa_circ_197531,RMVar_hsa_circ_303639,RMVar_hsa_circ_283325,RMVar_hsa_circ_197536,RMVar_hsa_circ_197534 88782 RMVar_ID_88782 Human_SNP_ID_63905404 m1A Human chr2 - 23927015 23927015 23927015 GCGGCTCCGCTCGGCTCCCGCTGAGGAGGGCGAAGCCGGCGGAGTGTCTGTGCTGCCGGTCTGCA GCGGCTCCGCTCGGCTCCCGCTGAGGAGGGCGCAGCCGGCGGAGTGTCTGTGCTGCCGGTCTGCA T G ATAD2B Ensembl:ENSG00000119778 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23926818..23927047 26863196 MeRIP-seq:(Medium) rs1282750779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4601455 88783 RMVar_ID_88783 Human_SNP_ID_63905420 m1A Human chr2 - 23927054 23927054 23927054 AGCTCGAGAGCGAGAACGGGAGAGAAAGGGGTAGAAATGGCGGCTCCGCTCGGCTCCCGCTGAGG AGCTCGAGAGCGAGAACGGGAGAGAAAGGGGTGGAAATGGCGGCTCCGCTCGGCTCCCGCTGAGG T C ATAD2B Ensembl:ENSG00000119778 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:23926935..23927063 26863196 MeRIP-seq:(Medium) rs1179055532 Functional Loss SNV dbSNP153 33..33 33 - - - 88784 RMVar_ID_88784 Human_SNP_ID_63905556 m1A Human chr2 + 23927365 23927365 23927365 CAGGACGAGTTCGGGCGTGGAATTGGGCCTGAAGCCCTCATGCCCAGCCAGGCCTGAATGCCCCA CAGGACGAGTTCGGGCGTGGAATTGGGCCTGAGGCCCTCATGCCCAGCCAGGCCTGAATGCCCCA A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:23927315..23927506 26863196 MeRIP-seq:(Medium) rs989673956 Functional Loss SNV dbSNP153 33..33 33 - - - 88785 RMVar_ID_88785 Human_SNP_ID_63908951 m1A Human chr2 - 23940526 23940526 23940526 AGAGCCGGAGCGCCGCCGCCCCAGACCGCCTCAGGTTCCGCGGCCGCGCCGCTGAGATCCCGCCA AGAGCCGGAGCGCCGCCGCCCCAGACCGCCTCTGGTTCCGCGGCCGCGCCGCTGAGATCCCGCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:23940476..23940830;chr2:23940476..23940694 26863196 MeRIP-seq:(Medium) rs1185084923 Functional Loss SNV dbSNP153 33..33 33 - - - 88786 RMVar_ID_88786 Human_SNP_ID_63913532 m1A Human chr2 + 23958233 23958233 23958233 CTTTAGACACTTTTAAGTAATACTTTAGGACTACATGGTAACTTACATATTAAGCTTTTTACTTA CTTTAGACACTTTTAAGTAATACTTTAGGACTGCATGGTAACTTACATATTAAGCTTTTTACTTA A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:23958226..23958318 26863196 MeRIP-seq:(Medium) rs1170914082 Functional Loss SNV dbSNP153 33..33 33 - - - 88787 RMVar_ID_88787 Human_SNP_ID_63913533 m1A Human chr2 + 23958233 23958233 23958233 CTTTAGACACTTTTAAGTAATACTTTAGGACTACATGGTAACTTACATATTAAGCTTTTTACTTA CTTTAGACACTTTTAAGTAATACTTTAGGACTTCATGGTAACTTACATATTAAGCTTTTTACTTA A T UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:23958226..23958318 26863196 MeRIP-seq:(Medium) rs1170914082 Functional Loss SNV dbSNP153 33..33 33 - - - 88788 RMVar_ID_88788 Human_SNP_ID_63931560 m1A Human chr2 - 24029552 24029552 24029552 AAGCACAGGCAATGTCTGTAATCAGCTGTGGGAGAGCAGTGACTGAGAACAGTCTGAGGCCTGGC AAGCACAGGCAATGTCTGTAATCAGCTGTGGGGGAGCAGTGACTGAGAACAGTCTGAGGCCTGGC T C WDCP Ensembl:ENSG00000163026 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24029501..24029586 26863196 MeRIP-seq:(Medium) rs561342325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26481102 88789 RMVar_ID_88789 Human_SNP_ID_63936725 m1A Human chr2 - 24049840 24049840 24049840 ATGGTCTCGATCTCCACGCCCATAGCGGTCCCACAGGCCCCGCCTCTGGGGGGTCCCTGCTGCTG ATGGTCTCGATCTCCACGCCCATAGCGGTCCCGCAGGCCCCGCCTCTGGGGGGTCCCTGCTGCTG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:24049740..24049867 26863410 MeRIP-seq:(Medium) rs776015111 Functional Loss SNV dbSNP153 33..33 33 - - - 88790 RMVar_ID_88790 Human_SNP_ID_63936730 m1A Human chr2 + 24049850 24049850 24049850 GACCCCCCAGAGGCGGGGCCTGTGGGACCGCTATGGGCGTGGAGATCGAGACCATCTCCCCCGGA GACCCCCCAGAGGCGGGGCCTGTGGGACCGCTGTGGGCGTGGAGATCGAGACCATCTCCCCCGGA A G FKBP1B,MFSD2B Ensembl:ENSG00000119782,Ensembl:ENSG00000205639 Protein coding,Protein coding start codon,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:24049749..24053913 26863410 MeRIP-seq:(Medium) rs761080358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4603318,Human_RBP_ID_9430016 Human_Splice_Rec_222529,Human_Splice_Rec_222535,Human_Splice_Rec_222545,Human_Splice_Rec_222551,Human_Splice_Rec_222557 RMVar_hsa_circ_197554 88791 RMVar_ID_88791 Human_SNP_ID_63941246 m1A Human chr2 - 24068461 24068460 24068461 GTATATCTTAATTAAGTTTAACTTACCTCTCCAGGGGGAACACACCTGAAACTAGAGGAACAGCT GTATATCTTAATTAAGTTTAACTTACCTCTCC_GGGGGAACACACCTGAAACTAGAGGAACAGCT CT C SF3B6 Ensembl:ENSG00000115128 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:24067683..24073691 32194978 MeRIP-seq:(Medium) rs1456601797 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_917642,Human_RBP_ID_22074479 RMVar_hsa_circ_92701,RMVar_hsa_circ_197560,RMVar_hsa_circ_197561,RMVar_hsa_circ_298485 88792 RMVar_ID_88792 Human_SNP_ID_63943036 m1A Human chr2 - 24076281 24076281 24076281 ATCTAACGCGGTGTAACCCCCGAAGCCGAGCGAGCTCCGGAGGAATTTCAGTATCTGCTACGGTA ATCTAACGCGGTGTAACCCCCGAAGCCGAGCGGGCTCCGGAGGAATTTCAGTATCTGCTACGGTA T C SF3B6 Ensembl:ENSG00000115128 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1201166407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547548,Human_RBP_ID_775016,Human_RBP_ID_1585271,Human_RBP_ID_1914190,Human_RBP_ID_4623148,Human_RBP_ID_5444707,Human_RBP_ID_5470650,Human_RBP_ID_18421710,Human_RBP_ID_22451125,Human_RBP_ID_22815237,Human_RBP_ID_23863106 Human_Splice_Rec_222571,Human_Splice_Rec_222577 RMVar_hsa_circ_92701,RMVar_hsa_circ_197560 88793 RMVar_ID_88793 Human_SNP_ID_63943038 m1A Human chr2 - 24076285 24076285 24076285 CTGCATCTAACGCGGTGTAACCCCCGAAGCCGAGCGAGCTCCGGAGGAATTTCAGTATCTGCTAC CTGCATCTAACGCGGTGTAACCCCCGAAGCCGTGCGAGCTCCGGAGGAATTTCAGTATCTGCTAC T A SF3B6 Ensembl:ENSG00000115128 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK-293T cells,m1A-IP-seq;HTR8/Svneo,Normoxia chr2:24074076..24076375 31548705,32194978 m1A-IP-seq:(High) rs1353636711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547549,Human_RBP_ID_775016,Human_RBP_ID_4623148,Human_RBP_ID_9104800,Human_RBP_ID_18421710,Human_RBP_ID_22451125,Human_RBP_ID_22815237 Human_Splice_Rec_222571,Human_Splice_Rec_222577 RMVar_hsa_circ_92701,RMVar_hsa_circ_197560 88794 RMVar_ID_88794 Human_SNP_ID_63943044 m1A Human chr2 + 24076302 24076302 24076302 TCCTCCGGAGCTCGCTCGGCTTCGGGGGTTACACCGCGTTAGATGCAGGACATCAACATCCAGGA TCCTCCGGAGCTCGCTCGGCTTCGGGGGTTACCCCGCGTTAGATGCAGGACATCAACATCCAGGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:24076251..24076350 26863196 MeRIP-seq:(Medium) rs1440413127 Functional Loss SNV dbSNP153 33..33 33 - - - 88795 RMVar_ID_88795 Human_SNP_ID_63943491 m1A Human chr2 + 24077685 24077685 24077685 CGGTCACTGGGTAGATTCTGTCCAGAACCGGCAGCAGACGTTGGGGGCCCTCCGTGGAGAAGTGA CGGTCACTGGGTAGATTCTGTCCAGAACCGGCGGCAGACGTTGGGGGCCCTCCGTGGAGAAGTGA A G FAM228B Ensembl:ENSG00000219626 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:24077580..24079607 32194978 MeRIP-seq:(Medium) rs1457022252 Functional Loss SNV dbSNP153 33..33 33 - - - 88796 RMVar_ID_88796 Human_SNP_ID_63945187 m1A Human chr2 - 24084297 24084297 24084297 AATATGTTAGCCGTGCACTTTGACAAGCCGGGAGGACCGGAAAACCTCTACGTGAAGGAGGTGGC AATATGTTAGCCGTGCACTTTGACAAGCCGGGGGGACCGGAAAACCTCTACGTGAAGGAGGTGGC T C TP53I3 Ensembl:ENSG00000115129 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:24084247..24084366;chr2:24084251..24084379 26863196 MeRIP-seq:(Medium) rs1225918237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19001255 Human_Splice_Rec_222684 88797 RMVar_ID_88797 Human_SNP_ID_63954462 m1A Human chr2 + 24123821 24123821 24123821 GTGGGTGGGAGGAAGGGCCGGGAGTGGGCGCGATGAGCGAGAGCGGGTGCGGACGCCTACGACAT GTGGGTGGGAGGAAGGGCCGGGAGTGGGCGCGGTGAGCGAGAGCGGGTGCGGACGCCTACGACAT A G FAM228B Ensembl:ENSG00000219626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24123770..24123901 26863196 MeRIP-seq:(Medium) rs577490214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777604 88798 RMVar_ID_88798 Human_SNP_ID_63974459 m1A Human chr2 - 24205574 24205574 24205574 ATAAGCGAGGGATACTGGATGCAGAGGAGGGAAGGGATCTGGGAGGTAGATGTGGGATCAGACCT ATAAGCGAGGGATACTGGATGCAGAGGAGGGACGGGATCTGGGAGGTAGATGTGGGATCAGACCT T G ITSN2 Ensembl:ENSG00000198399 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:24205527..24205634 26863196 MeRIP-seq:(Medium) rs980410484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362511 88799 RMVar_ID_88799 Human_SNP_ID_63975024 m1A Human chr2 + 24207572 24207572 24207572 GTCCCCGAGGGAGAGCGCTACAGAGGTCGGGGAGAGGCCTGGGCAAGGGTGGAAGAAGAACTGGG GTCCCCGAGGGAGAGCGCTACAGAGGTCGGGGGGAGGCCTGGGCAAGGGTGGAAGAAGAACTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:24207532..24207607 26863196 MeRIP-seq:(Medium) rs1300956353 Functional Loss SNV dbSNP153 33..33 33 - - - 88800 RMVar_ID_88800 Human_SNP_ID_63990288 m1A Human chr2 - 24271857 24271857 24271857 GAAGAAGAAAAACAAAAGCGACTCCAGGAAGAAAAAACACAAGAAAAAATTCAAGAAGAGGAACG GAAGAAGAAAAACAAAAGCGACTCCAGGAAGAGAAAACACAAGAAAAAATTCAAGAAGAGGAACG T C ITSN2 Ensembl:ENSG00000198399 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24271808..24275736 26863196 MeRIP-seq:(Medium) rs768045151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_917646,Human_RBP_ID_2632950,Human_RBP_ID_24546014,Human_RBP_ID_26339046,Human_RBP_ID_27818274 Human_Splice_Rec_222844,Human_Splice_Rec_222845,Human_Splice_Rec_222922,Human_Splice_Rec_222923,Human_Splice_Rec_222996,Human_Splice_Rec_222997,Human_Splice_Rec_223094,Human_Splice_Rec_223095 RMVar_hsa_circ_9870,RMVar_hsa_circ_92635,RMVar_hsa_circ_197574,RMVar_hsa_circ_108394,RMVar_hsa_circ_324411,RMVar_hsa_circ_197575,RMVar_hsa_circ_76375,RMVar_hsa_circ_334896,RMVar_hsa_circ_358229,RMVar_hsa_circ_326918,RMVar_hsa_circ_273486,RMVar_hsa_circ_25670,RMVar_hsa_circ_64044,RMVar_hsa_circ_19409,RMVar_hsa_circ_58824,RMVar_hsa_circ_41869,RMVar_hsa_circ_197582,RMVar_hsa_circ_197583,RMVar_hsa_circ_197584,RMVar_hsa_circ_197581,RMVar_hsa_circ_31690,RMVar_hsa_circ_127162,RMVar_hsa_circ_273355,RMVar_hsa_circ_354671,RMVar_hsa_circ_267842,RMVar_hsa_circ_62206,RMVar_hsa_circ_197585,RMVar_hsa_circ_42993,RMVar_hsa_circ_52638,RMVar_hsa_circ_197586,RMVar_hsa_circ_54443,RMVar_hsa_circ_267978,RMVar_hsa_circ_302410,RMVar_hsa_circ_80258,RMVar_hsa_circ_197588,RMVar_hsa_circ_21718,RMVar_hsa_circ_197587,RMVar_hsa_circ_25423,RMVar_hsa_circ_286647,RMVar_hsa_circ_306732,RMVar_hsa_circ_376042,RMVar_hsa_circ_197589,RMVar_hsa_circ_336554,RMVar_hsa_circ_303560,RMVar_hsa_circ_58908,RMVar_hsa_circ_65335,RMVar_hsa_circ_43377,RMVar_hsa_circ_197590,RMVar_hsa_circ_197592,RMVar_hsa_circ_197593,RMVar_hsa_circ_197594,RMVar_hsa_circ_197591 88801 RMVar_ID_88801 Human_SNP_ID_63996573 m1A Human chr2 - 24298809 24298809 24298809 TTAAGTATAATTCCTTTTTTTTTTCAGGCAGCAAAACAGGAACTTGAACGACAACGTCGCTTAGA TTAAGTATAATTCCTTTTTTTTTTCAGGCAGCGAAACAGGAACTTGAACGACAACGTCGCTTAGA T C ITSN2 Ensembl:ENSG00000198399 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24298758..24298882 26863196 MeRIP-seq:(Medium) rs754284181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60527,Human_RBP_ID_917650,Human_RBP_ID_26340709 Human_Splice_Rec_222834,Human_Splice_Rec_222910,Human_Splice_Rec_222986,Human_Splice_Rec_223082,Human_Splice_Rec_223148 RMVar_hsa_circ_7335,RMVar_hsa_circ_9870,RMVar_hsa_circ_92635,RMVar_hsa_circ_197574,RMVar_hsa_circ_108394,RMVar_hsa_circ_324411,RMVar_hsa_circ_197575,RMVar_hsa_circ_76375,RMVar_hsa_circ_334896,RMVar_hsa_circ_326918,RMVar_hsa_circ_64044,RMVar_hsa_circ_19409,RMVar_hsa_circ_58824,RMVar_hsa_circ_41869,RMVar_hsa_circ_197583,RMVar_hsa_circ_197584,RMVar_hsa_circ_31690,RMVar_hsa_circ_127162,RMVar_hsa_circ_273355,RMVar_hsa_circ_267842,RMVar_hsa_circ_62206,RMVar_hsa_circ_197585,RMVar_hsa_circ_52638,RMVar_hsa_circ_197586,RMVar_hsa_circ_267978,RMVar_hsa_circ_302410,RMVar_hsa_circ_80258,RMVar_hsa_circ_197588,RMVar_hsa_circ_197587,RMVar_hsa_circ_286647,RMVar_hsa_circ_376042,RMVar_hsa_circ_197589,RMVar_hsa_circ_336554,RMVar_hsa_circ_65335,RMVar_hsa_circ_43377,RMVar_hsa_circ_197592,RMVar_hsa_circ_197593,RMVar_hsa_circ_197594,RMVar_hsa_circ_46707,RMVar_hsa_circ_300322,RMVar_hsa_circ_52212,RMVar_hsa_circ_29842,RMVar_hsa_circ_197596,RMVar_hsa_circ_361420,RMVar_hsa_circ_54680,RMVar_hsa_circ_64452,RMVar_hsa_circ_197597,RMVar_hsa_circ_69839,RMVar_hsa_circ_61862,RMVar_hsa_circ_71477,RMVar_hsa_circ_338117,RMVar_hsa_circ_359972,RMVar_hsa_circ_72674,RMVar_hsa_circ_29338,RMVar_hsa_circ_62698,RMVar_hsa_circ_341306,RMVar_hsa_circ_357222 88802 RMVar_ID_88802 Human_SNP_ID_64003812 m1A Human chr2 - 24328115 24328115 24328115 ATTATCAACGGCACAATATTTTTATGTTGCAGATGGCTGAGAGCTAGCAAGGAAAACTCAGGACC ATTATCAACGGCACAATATTTTTATGTTGCAGTTGGCTGAGAGCTAGCAAGGAAAACTCAGGACC T A ITSN2 Ensembl:ENSG00000198399 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24328103..24328168 26863196 MeRIP-seq:(Medium) rs1284821393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778347,Human_RBP_ID_13829413,Human_RBP_ID_19001257 Human_Splice_Rec_222812,Human_Splice_Rec_222813,Human_Splice_Rec_222888,Human_Splice_Rec_222889,Human_Splice_Rec_222965,Human_Splice_Rec_223060,Human_Splice_Rec_223061,Human_Splice_Rec_223124,Human_Splice_Rec_223125,Human_Splice_Rec_223158,Human_Splice_Rec_223159,Human_Splice_Rec_223174,Human_Splice_Rec_223175 RMVar_hsa_circ_326918,RMVar_hsa_circ_19409,RMVar_hsa_circ_52638,RMVar_hsa_circ_267978,RMVar_hsa_circ_197589,RMVar_hsa_circ_64452,RMVar_hsa_circ_17198,RMVar_hsa_circ_49681,RMVar_hsa_circ_114320,RMVar_hsa_circ_197602,RMVar_hsa_circ_361078 88803 RMVar_ID_88803 Human_SNP_ID_64003813 m1A Human chr2 - 24328115 24328115 24328115 ATTATCAACGGCACAATATTTTTATGTTGCAGATGGCTGAGAGCTAGCAAGGAAAACTCAGGACC ATTATCAACGGCACAATATTTTTATGTTGCAGGTGGCTGAGAGCTAGCAAGGAAAACTCAGGACC T C ITSN2 Ensembl:ENSG00000198399 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24328103..24328168 26863196 MeRIP-seq:(Medium) rs1284821393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778347,Human_RBP_ID_13829413,Human_RBP_ID_19001257 Human_Splice_Rec_222812,Human_Splice_Rec_222813,Human_Splice_Rec_222888,Human_Splice_Rec_222889,Human_Splice_Rec_222965,Human_Splice_Rec_223060,Human_Splice_Rec_223061,Human_Splice_Rec_223124,Human_Splice_Rec_223125,Human_Splice_Rec_223158,Human_Splice_Rec_223159,Human_Splice_Rec_223174,Human_Splice_Rec_223175 RMVar_hsa_circ_326918,RMVar_hsa_circ_19409,RMVar_hsa_circ_52638,RMVar_hsa_circ_267978,RMVar_hsa_circ_197589,RMVar_hsa_circ_64452,RMVar_hsa_circ_17198,RMVar_hsa_circ_49681,RMVar_hsa_circ_114320,RMVar_hsa_circ_197602,RMVar_hsa_circ_361078 88804 RMVar_ID_88804 Human_SNP_ID_64011829 m1A Human chr2 - 24360329 24360329 24360329 GGTGCTGAGGGACGCGGAGTCGCGCTGTGACGAGCGGGAGGCGCGGCGAGGGCGCCAGGTGGGTG GGTGCTGAGGGACGCGGAGTCGCGCTGTGACGTGCGGGAGGCGCGGCGAGGGCGCCAGGTGGGTG T A ITSN2 Ensembl:ENSG00000198399 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:24360314..24360476 26863196 MeRIP-seq:(Medium) rs4332878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777564,Human_RBP_ID_9297051 Human_Splice_Rec_222811,Human_Splice_Rec_222887,Human_Splice_Rec_223059,Human_Splice_Rec_223123,Human_Splice_Rec_223157,Human_Splice_Rec_223173 GWAS_ID_11172,GWAS_ID_11173,GWAS_ID_11174,GWAS_ID_11175,GWAS_ID_11176,GWAS_ID_11177,GWAS_ID_11178,GWAS_ID_11179,GWAS_ID_11180,GWAS_ID_11181,GWAS_ID_11182,GWAS_ID_11183,GWAS_ID_11184,GWAS_ID_11185,GWAS_ID_11186,GWAS_ID_11187,GWAS_ID_11188,GWAS_ID_11189,GWAS_ID_11190,GWAS_ID_11191,GWAS_ID_11192,GWAS_ID_11193,GWAS_ID_11194,GWAS_ID_11195,GWAS_ID_11196,GWAS_ID_11197,GWAS_ID_11198,GWAS_ID_11199,GWAS_ID_11200,GWAS_ID_11201,GWAS_ID_11202,GWAS_ID_11203,GWAS_ID_11204,GWAS_ID_11205,GWAS_ID_11206,GWAS_ID_11207,GWAS_ID_11208,GWAS_ID_11209,GWAS_ID_11210,GWAS_ID_11211,GWAS_ID_11212,GWAS_ID_11213,GWAS_ID_11214,GWAS_ID_11215,GWAS_ID_11216,GWAS_ID_11217,GWAS_ID_11218,GWAS_ID_11219,GWAS_ID_11220,GWAS_ID_11221,GWAS_ID_11222,GWAS_ID_11223,GWAS_ID_11224,GWAS_ID_11225,GWAS_ID_11226,GWAS_ID_11227,GWAS_ID_11228,GWAS_ID_11229,GWAS_ID_11230,GWAS_ID_11231,GWAS_ID_11232,GWAS_ID_11233,GWAS_ID_11234,GWAS_ID_11235,GWAS_ID_11236,GWAS_ID_11237,GWAS_ID_11238,GWAS_ID_11239,GWAS_ID_11240,GWAS_ID_11241,GWAS_ID_11242,GWAS_ID_11243,GWAS_ID_11244,GWAS_ID_11245,GWAS_ID_11246,GWAS_ID_11247,GWAS_ID_11248,GWAS_ID_11249,GWAS_ID_11250,GWAS_ID_11251,GWAS_ID_11252,GWAS_ID_11253,GWAS_ID_11254,GWAS_ID_11255,GWAS_ID_11256,GWAS_ID_11257,GWAS_ID_11258,GWAS_ID_11259,GWAS_ID_11260,GWAS_ID_11261,GWAS_ID_11262,GWAS_ID_11263,GWAS_ID_11264,GWAS_ID_11265,GWAS_ID_11266,GWAS_ID_11267,GWAS_ID_11268,GWAS_ID_11269,GWAS_ID_11270,GWAS_ID_11271,GWAS_ID_11272,GWAS_ID_11273,GWAS_ID_11274,GWAS_ID_11275,GWAS_ID_11276,GWAS_ID_11277,GWAS_ID_11278,GWAS_ID_11279,GWAS_ID_11280,GWAS_ID_11281,GWAS_ID_11282,GWAS_ID_11283,GWAS_ID_11284,GWAS_ID_11285,GWAS_ID_11286,GWAS_ID_11287,GWAS_ID_11288,GWAS_ID_11289,GWAS_ID_11290,GWAS_ID_11291,GWAS_ID_11292,GWAS_ID_11293,GWAS_ID_11294,GWAS_ID_11295,GWAS_ID_11296,GWAS_ID_11297,GWAS_ID_11298,GWAS_ID_11299,GWAS_ID_11300,GWAS_ID_11301,GWAS_ID_11302,GWAS_ID_11303,GWAS_ID_11304,GWAS_ID_11305,GWAS_ID_11306,GWAS_ID_11307,GWAS_ID_11308,GWAS_ID_11309,GWAS_ID_11310,GWAS_ID_11311,GWAS_ID_11312,GWAS_ID_11313,GWAS_ID_11314,GWAS_ID_11315,GWAS_ID_11316,GWAS_ID_11317,GWAS_ID_11318,GWAS_ID_11319,GWAS_ID_11320,GWAS_ID_11321,GWAS_ID_11322,GWAS_ID_11323,GWAS_ID_11324,GWAS_ID_11325,GWAS_ID_11326,GWAS_ID_11327,GWAS_ID_11328,GWAS_ID_11329,GWAS_ID_11330,GWAS_ID_11331,GWAS_ID_11332,GWAS_ID_11333,GWAS_ID_11334,GWAS_ID_11335,GWAS_ID_11336,GWAS_ID_11337,GWAS_ID_11338,GWAS_ID_11339,GWAS_ID_11340,GWAS_ID_11341,GWAS_ID_11342,GWAS_ID_11343,GWAS_ID_11344,GWAS_ID_11345,GWAS_ID_11346,GWAS_ID_11347,GWAS_ID_11348,GWAS_ID_11349,GWAS_ID_11350,GWAS_ID_11351,GWAS_ID_11352,GWAS_ID_11353,GWAS_ID_11354,GWAS_ID_11355,GWAS_ID_11356,GWAS_ID_11357,GWAS_ID_11358,GWAS_ID_11359,GWAS_ID_11360,GWAS_ID_11361,GWAS_ID_11362,GWAS_ID_11363,GWAS_ID_11364,GWAS_ID_11365,GWAS_ID_11366,GWAS_ID_11367,GWAS_ID_11368,GWAS_ID_11369,GWAS_ID_11370,GWAS_ID_11371,GWAS_ID_11372,GWAS_ID_11373,GWAS_ID_11374,GWAS_ID_11375,GWAS_ID_11376,GWAS_ID_11377,GWAS_ID_11378,GWAS_ID_11379,GWAS_ID_11380,GWAS_ID_11381,GWAS_ID_11382,GWAS_ID_11383,GWAS_ID_11384,GWAS_ID_11385,GWAS_ID_11386,GWAS_ID_11387,GWAS_ID_11388,GWAS_ID_11389,GWAS_ID_11390,GWAS_ID_11391,GWAS_ID_11392,GWAS_ID_11393,GWAS_ID_11394,GWAS_ID_11395,GWAS_ID_11396,GWAS_ID_11397,GWAS_ID_11398,GWAS_ID_11399,GWAS_ID_11400,GWAS_ID_11401,GWAS_ID_11402,GWAS_ID_11403,GWAS_ID_11404,GWAS_ID_11405,GWAS_ID_11406,GWAS_ID_11407,GWAS_ID_11408,GWAS_ID_11409,GWAS_ID_11410,GWAS_ID_11411,GWAS_ID_11412,GWAS_ID_11413,GWAS_ID_11414,GWAS_ID_11415,GWAS_ID_11416,GWAS_ID_11417,GWAS_ID_11418,GWAS_ID_11419,GWAS_ID_11420,GWAS_ID_11421,GWAS_ID_11422,GWAS_ID_11423,GWAS_ID_11424,GWAS_ID_11425,GWAS_ID_11426,GWAS_ID_11427,GWAS_ID_11428,GWAS_ID_11429,GWAS_ID_11430,GWAS_ID_11431,GWAS_ID_11432,GWAS_ID_11433,GWAS_ID_11434,GWAS_ID_11435,GWAS_ID_11436,GWAS_ID_11437,GWAS_ID_11438,GWAS_ID_11439,GWAS_ID_11440,GWAS_ID_11441,GWAS_ID_11442,GWAS_ID_11443,GWAS_ID_11444,GWAS_ID_11445,GWAS_ID_11446,GWAS_ID_11447,GWAS_ID_11448,GWAS_ID_11449,GWAS_ID_11450,GWAS_ID_11451,GWAS_ID_11452,GWAS_ID_11453,GWAS_ID_11454,GWAS_ID_11455,GWAS_ID_11456,GWAS_ID_11457,GWAS_ID_11458,GWAS_ID_11459,GWAS_ID_11460,GWAS_ID_11461,GWAS_ID_11462,GWAS_ID_11463,GWAS_ID_11464,GWAS_ID_11465,GWAS_ID_11466,GWAS_ID_11467,GWAS_ID_11468,GWAS_ID_11469,GWAS_ID_11470,GWAS_ID_11471,GWAS_ID_11472,GWAS_ID_11473,GWAS_ID_11474,GWAS_ID_11475,GWAS_ID_11476,GWAS_ID_11477,GWAS_ID_11478,GWAS_ID_11479,GWAS_ID_11480,GWAS_ID_11481,GWAS_ID_11482,GWAS_ID_11483,GWAS_ID_11484,GWAS_ID_11485,GWAS_ID_11486,GWAS_ID_11487,GWAS_ID_11488,GWAS_ID_11489,GWAS_ID_11490,GWAS_ID_11491,GWAS_ID_11492,GWAS_ID_11493,GWAS_ID_11494,GWAS_ID_11495,GWAS_ID_11496,GWAS_ID_11497,GWAS_ID_11498,GWAS_ID_11499,GWAS_ID_11500,GWAS_ID_11501,GWAS_ID_11502,GWAS_ID_11503,GWAS_ID_11504,GWAS_ID_11505,GWAS_ID_11506,GWAS_ID_11507,GWAS_ID_11508,GWAS_ID_11509,GWAS_ID_11510,GWAS_ID_11511,GWAS_ID_11512,GWAS_ID_11513,GWAS_ID_11514,GWAS_ID_11515,GWAS_ID_11516,GWAS_ID_11517,GWAS_ID_11518,GWAS_ID_11519,GWAS_ID_11520,GWAS_ID_11521,GWAS_ID_11522,GWAS_ID_11523,GWAS_ID_11524,GWAS_ID_11525,GWAS_ID_11526,GWAS_ID_11527,GWAS_ID_11528,GWAS_ID_11529,GWAS_ID_11530,GWAS_ID_11531,GWAS_ID_11532,GWAS_ID_11533,GWAS_ID_11534,GWAS_ID_11535,GWAS_ID_11536,GWAS_ID_11537,GWAS_ID_11538,GWAS_ID_11539,GWAS_ID_11540 88805 RMVar_ID_88805 Human_SNP_ID_64011830 m1A Human chr2 - 24360329 24360329 24360329 GGTGCTGAGGGACGCGGAGTCGCGCTGTGACGAGCGGGAGGCGCGGCGAGGGCGCCAGGTGGGTG GGTGCTGAGGGACGCGGAGTCGCGCTGTGACGGGCGGGAGGCGCGGCGAGGGCGCCAGGTGGGTG T C ITSN2 Ensembl:ENSG00000198399 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:24360314..24360476 26863196 MeRIP-seq:(Medium) rs4332878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777564,Human_RBP_ID_9297051 Human_Splice_Rec_222811,Human_Splice_Rec_222887,Human_Splice_Rec_223059,Human_Splice_Rec_223123,Human_Splice_Rec_223157,Human_Splice_Rec_223173 GWAS_ID_11172,GWAS_ID_11173,GWAS_ID_11174,GWAS_ID_11175,GWAS_ID_11176,GWAS_ID_11177,GWAS_ID_11178,GWAS_ID_11179,GWAS_ID_11180,GWAS_ID_11181,GWAS_ID_11182,GWAS_ID_11183,GWAS_ID_11184,GWAS_ID_11185,GWAS_ID_11186,GWAS_ID_11187,GWAS_ID_11188,GWAS_ID_11189,GWAS_ID_11190,GWAS_ID_11191,GWAS_ID_11192,GWAS_ID_11193,GWAS_ID_11194,GWAS_ID_11195,GWAS_ID_11196,GWAS_ID_11197,GWAS_ID_11198,GWAS_ID_11199,GWAS_ID_11200,GWAS_ID_11201,GWAS_ID_11202,GWAS_ID_11203,GWAS_ID_11204,GWAS_ID_11205,GWAS_ID_11206,GWAS_ID_11207,GWAS_ID_11208,GWAS_ID_11209,GWAS_ID_11210,GWAS_ID_11211,GWAS_ID_11212,GWAS_ID_11213,GWAS_ID_11214,GWAS_ID_11215,GWAS_ID_11216,GWAS_ID_11217,GWAS_ID_11218,GWAS_ID_11219,GWAS_ID_11220,GWAS_ID_11221,GWAS_ID_11222,GWAS_ID_11223,GWAS_ID_11224,GWAS_ID_11225,GWAS_ID_11226,GWAS_ID_11227,GWAS_ID_11228,GWAS_ID_11229,GWAS_ID_11230,GWAS_ID_11231,GWAS_ID_11232,GWAS_ID_11233,GWAS_ID_11234,GWAS_ID_11235,GWAS_ID_11236,GWAS_ID_11237,GWAS_ID_11238,GWAS_ID_11239,GWAS_ID_11240,GWAS_ID_11241,GWAS_ID_11242,GWAS_ID_11243,GWAS_ID_11244,GWAS_ID_11245,GWAS_ID_11246,GWAS_ID_11247,GWAS_ID_11248,GWAS_ID_11249,GWAS_ID_11250,GWAS_ID_11251,GWAS_ID_11252,GWAS_ID_11253,GWAS_ID_11254,GWAS_ID_11255,GWAS_ID_11256,GWAS_ID_11257,GWAS_ID_11258,GWAS_ID_11259,GWAS_ID_11260,GWAS_ID_11261,GWAS_ID_11262,GWAS_ID_11263,GWAS_ID_11264,GWAS_ID_11265,GWAS_ID_11266,GWAS_ID_11267,GWAS_ID_11268,GWAS_ID_11269,GWAS_ID_11270,GWAS_ID_11271,GWAS_ID_11272,GWAS_ID_11273,GWAS_ID_11274,GWAS_ID_11275,GWAS_ID_11276,GWAS_ID_11277,GWAS_ID_11278,GWAS_ID_11279,GWAS_ID_11280,GWAS_ID_11281,GWAS_ID_11282,GWAS_ID_11283,GWAS_ID_11284,GWAS_ID_11285,GWAS_ID_11286,GWAS_ID_11287,GWAS_ID_11288,GWAS_ID_11289,GWAS_ID_11290,GWAS_ID_11291,GWAS_ID_11292,GWAS_ID_11293,GWAS_ID_11294,GWAS_ID_11295,GWAS_ID_11296,GWAS_ID_11297,GWAS_ID_11298,GWAS_ID_11299,GWAS_ID_11300,GWAS_ID_11301,GWAS_ID_11302,GWAS_ID_11303,GWAS_ID_11304,GWAS_ID_11305,GWAS_ID_11306,GWAS_ID_11307,GWAS_ID_11308,GWAS_ID_11309,GWAS_ID_11310,GWAS_ID_11311,GWAS_ID_11312,GWAS_ID_11313,GWAS_ID_11314,GWAS_ID_11315,GWAS_ID_11316,GWAS_ID_11317,GWAS_ID_11318,GWAS_ID_11319,GWAS_ID_11320,GWAS_ID_11321,GWAS_ID_11322,GWAS_ID_11323,GWAS_ID_11324,GWAS_ID_11325,GWAS_ID_11326,GWAS_ID_11327,GWAS_ID_11328,GWAS_ID_11329,GWAS_ID_11330,GWAS_ID_11331,GWAS_ID_11332,GWAS_ID_11333,GWAS_ID_11334,GWAS_ID_11335,GWAS_ID_11336,GWAS_ID_11337,GWAS_ID_11338,GWAS_ID_11339,GWAS_ID_11340,GWAS_ID_11341,GWAS_ID_11342,GWAS_ID_11343,GWAS_ID_11344,GWAS_ID_11345,GWAS_ID_11346,GWAS_ID_11347,GWAS_ID_11348,GWAS_ID_11349,GWAS_ID_11350,GWAS_ID_11351,GWAS_ID_11352,GWAS_ID_11353,GWAS_ID_11354,GWAS_ID_11355,GWAS_ID_11356,GWAS_ID_11357,GWAS_ID_11358,GWAS_ID_11359,GWAS_ID_11360,GWAS_ID_11361,GWAS_ID_11362,GWAS_ID_11363,GWAS_ID_11364,GWAS_ID_11365,GWAS_ID_11366,GWAS_ID_11367,GWAS_ID_11368,GWAS_ID_11369,GWAS_ID_11370,GWAS_ID_11371,GWAS_ID_11372,GWAS_ID_11373,GWAS_ID_11374,GWAS_ID_11375,GWAS_ID_11376,GWAS_ID_11377,GWAS_ID_11378,GWAS_ID_11379,GWAS_ID_11380,GWAS_ID_11381,GWAS_ID_11382,GWAS_ID_11383,GWAS_ID_11384,GWAS_ID_11385,GWAS_ID_11386,GWAS_ID_11387,GWAS_ID_11388,GWAS_ID_11389,GWAS_ID_11390,GWAS_ID_11391,GWAS_ID_11392,GWAS_ID_11393,GWAS_ID_11394,GWAS_ID_11395,GWAS_ID_11396,GWAS_ID_11397,GWAS_ID_11398,GWAS_ID_11399,GWAS_ID_11400,GWAS_ID_11401,GWAS_ID_11402,GWAS_ID_11403,GWAS_ID_11404,GWAS_ID_11405,GWAS_ID_11406,GWAS_ID_11407,GWAS_ID_11408,GWAS_ID_11409,GWAS_ID_11410,GWAS_ID_11411,GWAS_ID_11412,GWAS_ID_11413,GWAS_ID_11414,GWAS_ID_11415,GWAS_ID_11416,GWAS_ID_11417,GWAS_ID_11418,GWAS_ID_11419,GWAS_ID_11420,GWAS_ID_11421,GWAS_ID_11422,GWAS_ID_11423,GWAS_ID_11424,GWAS_ID_11425,GWAS_ID_11426,GWAS_ID_11427,GWAS_ID_11428,GWAS_ID_11429,GWAS_ID_11430,GWAS_ID_11431,GWAS_ID_11432,GWAS_ID_11433,GWAS_ID_11434,GWAS_ID_11435,GWAS_ID_11436,GWAS_ID_11437,GWAS_ID_11438,GWAS_ID_11439,GWAS_ID_11440,GWAS_ID_11441,GWAS_ID_11442,GWAS_ID_11443,GWAS_ID_11444,GWAS_ID_11445,GWAS_ID_11446,GWAS_ID_11447,GWAS_ID_11448,GWAS_ID_11449,GWAS_ID_11450,GWAS_ID_11451,GWAS_ID_11452,GWAS_ID_11453,GWAS_ID_11454,GWAS_ID_11455,GWAS_ID_11456,GWAS_ID_11457,GWAS_ID_11458,GWAS_ID_11459,GWAS_ID_11460,GWAS_ID_11461,GWAS_ID_11462,GWAS_ID_11463,GWAS_ID_11464,GWAS_ID_11465,GWAS_ID_11466,GWAS_ID_11467,GWAS_ID_11468,GWAS_ID_11469,GWAS_ID_11470,GWAS_ID_11471,GWAS_ID_11472,GWAS_ID_11473,GWAS_ID_11474,GWAS_ID_11475,GWAS_ID_11476,GWAS_ID_11477,GWAS_ID_11478,GWAS_ID_11479,GWAS_ID_11480,GWAS_ID_11481,GWAS_ID_11482,GWAS_ID_11483,GWAS_ID_11484,GWAS_ID_11485,GWAS_ID_11486,GWAS_ID_11487,GWAS_ID_11488,GWAS_ID_11489,GWAS_ID_11490,GWAS_ID_11491,GWAS_ID_11492,GWAS_ID_11493,GWAS_ID_11494,GWAS_ID_11495,GWAS_ID_11496,GWAS_ID_11497,GWAS_ID_11498,GWAS_ID_11499,GWAS_ID_11500,GWAS_ID_11501,GWAS_ID_11502,GWAS_ID_11503,GWAS_ID_11504,GWAS_ID_11505,GWAS_ID_11506,GWAS_ID_11507,GWAS_ID_11508,GWAS_ID_11509,GWAS_ID_11510,GWAS_ID_11511,GWAS_ID_11512,GWAS_ID_11513,GWAS_ID_11514,GWAS_ID_11515,GWAS_ID_11516,GWAS_ID_11517,GWAS_ID_11518,GWAS_ID_11519,GWAS_ID_11520,GWAS_ID_11521,GWAS_ID_11522,GWAS_ID_11523,GWAS_ID_11524,GWAS_ID_11525,GWAS_ID_11526,GWAS_ID_11527,GWAS_ID_11528,GWAS_ID_11529,GWAS_ID_11530,GWAS_ID_11531,GWAS_ID_11532,GWAS_ID_11533,GWAS_ID_11534,GWAS_ID_11535,GWAS_ID_11536,GWAS_ID_11537,GWAS_ID_11538,GWAS_ID_11539,GWAS_ID_11540 88806 RMVar_ID_88806 Human_SNP_ID_64046734 m1A Human chr2 - 24491552 24491550 24491553 GGCCCCGCTCACCGGCGCCGCACTCGTCCGCGACCGTGGCGGCGGCGCCGCCCCGGCCTCCGCCG GGCCCCGCTCACCGGCGCCGCACTCGTCCGC___CGTGGCGGCGGCGCCGCCCCGGCCTCCGCCG GGTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24491271..24491586 26863196 MeRIP-seq:(Medium) rs1210374966 Functional Loss DEL dbSNP153 32..34 33 - - - 88807 RMVar_ID_88807 Human_SNP_ID_64112217 m1A Human chr2 - 24766715 24766711 24766715 TCCTCTCTTCCTAGGTCAACGATCCTCCTGCCAGCCCTCTTCCCGCTCCTCTCTTCTCTTCTTGT TCCTCTCTTCCTAGGTCAACGATCCTCCTGCC____CTCTTCCCGCTCCTCTCTTCTCTTCTTGT GGGCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24766594..24766828 26863196 MeRIP-seq:(Medium) rs1191598279 Functional Loss DEL dbSNP153 33..36 33 - - - 88808 RMVar_ID_88808 Human_SNP_ID_64117973 m1A Human chr2 - 24790533 24790533 24790533 CCCTAAAGGAGCTGGCCGAGACCCTGCAACAGAAGAACATTGACCACATGCTGTGGCTTGAGCAA CCCTAAAGGAGCTGGCCGAGACCCTGCAACAGGAGAACATTGACCACATGCTGTGGCTTGAGCAA T C PTRHD1 Ensembl:ENSG00000184924 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:24790483..24790622 26863196 MeRIP-seq:(Medium) rs138426814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547602,Human_RBP_ID_8516043,Human_RBP_ID_9330945,Human_RBP_ID_17658389,Human_RBP_ID_18193250,Human_RBP_ID_26819545 Human_Splice_Rec_223476,Human_Splice_Rec_223480,Human_Splice_Rec_223482,Human_Splice_Rec_223484,Human_Splice_Rec_223486 RMVar_hsa_circ_81237,RMVar_hsa_circ_197664 88809 RMVar_ID_88809 Human_SNP_ID_64119590 m1A Human chr2 - 24796771 24796771 24796771 TGCAGCTACTCTAGCTCGTTAGCACTCAATGCAAGCAGCATTTCCTCAGGGAAACCTTTGTAGCA TGCAGCTACTCTAGCTCGTTAGCACTCAATGCCAGCAGCATTTCCTCAGGGAAACCTTTGTAGCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:24796768..24796959 26863196 MeRIP-seq:(Medium) rs1449289070 Functional Loss SNV dbSNP153 33..33 33 - - - 88810 RMVar_ID_88810 Human_SNP_ID_64120372 m1A Human chr2 + 24799744 24799744 24799744 GAGCAGATCCCGTAAACAGTCTGAAGAGCTGCAGAGCGTGCAGGCCCAGGAAGGTGCTCTTGGAA GAGCAGATCCCGTAAACAGTCTGAAGAGCTGCGGAGCGTGCAGGCCCAGGAAGGTGCTCTTGGAA A G CENPO Ensembl:ENSG00000138092 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:24799695..24799807 26863196 MeRIP-seq:(Medium) rs1322959712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242845,Human_RBP_ID_915318,Human_RBP_ID_4603514,Human_RBP_ID_9386137,Human_RBP_ID_13830916,Human_RBP_ID_18757755 Human_Splice_Rec_223494,Human_Splice_Rec_223496,Human_Splice_Rec_223510,Human_Splice_Rec_223518,Human_Splice_Rec_223532,Human_Splice_Rec_223538,Human_Splice_Rec_223550 Human_miRNA_ID_2011344,Human_miRNA_ID_2011345,Human_miRNA_ID_2038566,Human_miRNA_ID_2038567,Human_miRNA_ID_2394339,Human_miRNA_ID_2394340,Human_miRNA_ID_2757700,Human_miRNA_ID_2757701,Human_miRNA_ID_3017548,Human_miRNA_ID_3017549 RMVar_hsa_circ_50671,RMVar_hsa_circ_102167,RMVar_hsa_circ_125266,RMVar_hsa_circ_197665,RMVar_hsa_circ_197666,RMVar_hsa_circ_273964,RMVar_hsa_circ_307338,RMVar_hsa_circ_50942,RMVar_hsa_circ_197668,RMVar_hsa_circ_45703 88811 RMVar_ID_88811 Human_SNP_ID_64132694 m1A Human chr2 - 24839979 24839979 24839979 AGACTGGGGTGGACATGCGTGTGGGGGTGCACACGGGCACCGTGCTGGGGGGCGTCCTGGGCCAG AGACTGGGGTGGACATGCGTGTGGGGGTGCACGCGGGCACCGTGCTGGGGGGCGTCCTGGGCCAG T C ADCY3 Ensembl:ENSG00000138031 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:24839882..24840053 26863196 MeRIP-seq:(Medium) rs866310946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3957644,Human_RBP_ID_4603719,Human_RBP_ID_26339066 Human_Splice_Rec_223580,Human_Splice_Rec_223614,Human_Splice_Rec_223656,Human_Splice_Rec_223712,Human_Splice_Rec_223726,Human_Splice_Rec_223740,Human_Splice_Rec_223750 Human_miRNA_ID_2468081 RMVar_hsa_circ_84336,RMVar_hsa_circ_197673,RMVar_hsa_circ_110222,RMVar_hsa_circ_197676,RMVar_hsa_circ_115791,RMVar_hsa_circ_52510,RMVar_hsa_circ_33668,RMVar_hsa_circ_197678 88812 RMVar_ID_88812 Human_SNP_ID_64147126 m1A Human chr2 - 24897101 24897101 24897101 GTGGGTGGCTGGTCTCTTTCTTCCTCTGATCTACCATGATGTCATCTTGCGAAAAGATGATGAGA GTGGGTGGCTGGTCTCTTTCTTCCTCTGATCTGCCATGATGTCATCTTGCGAAAAGATGATGAGA T C ADCY3 Ensembl:ENSG00000138031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24897098..24897215 26863196 MeRIP-seq:(Medium) rs557486080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84336,RMVar_hsa_circ_197673 88813 RMVar_ID_88813 Human_SNP_ID_64151341 m1A Human chr2 - 24912990 24912990 24912990 CCAGGGACCAGAACAATGATGACGTGCGTAGAAGGGGACTGCAGGGCCATCAGATTCAGCTGCAT CCAGGGACCAGAACAATGATGACGTGCGTAGAGGGGGACTGCAGGGCCATCAGATTCAGCTGCAT T C ADCY3 Ensembl:ENSG00000138031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24912985..24913104 26863196 MeRIP-seq:(Medium) rs796076515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6903270,Human_RBP_ID_13831965 RMVar_hsa_circ_84336,RMVar_hsa_circ_197673 88814 RMVar_ID_88814 Human_SNP_ID_64160222 m1A Human chr2 - 24948441 24948441 24948441 TCAGATTCCTCGTGACCTTGACCCTGGAGCTCATTTCAGCCCCTTTCTTTTCATCTTCTCCTCCT TCAGATTCCTCGTGACCTTGACCCTGGAGCTCGTTTCAGCCCCTTTCTTTTCATCTTCTCCTCCT T C DNAJC27 Ensembl:ENSG00000115137 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:24948313..24948440 26863196 MeRIP-seq:(Medium) rs1392331042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197680 88815 RMVar_ID_88815 Human_SNP_ID_64162767 m1A Human chr2 - 24959233 24959233 24959233 GCAATAGAGAGAAGGGGAGTTGGTGAAAGAGAATTTAAGAGCCTAGGGAATGTGATGTATGGGAG GCAATAGAGAGAAGGGGAGTTGGTGAAAGAGAGTTTAAGAGCCTAGGGAATGTGATGTATGGGAG T C DNAJC27 Ensembl:ENSG00000115137 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:24959195..24959329 26863196 MeRIP-seq:(Medium) rs900786021 Functional Loss SNV dbSNP153 33..33 33 - - - 88816 RMVar_ID_88816 Human_SNP_ID_64165989 m1A Human chr2 - 24971914 24971914 24971914 CAAGAAGAGACCGAGGCGGGTGGCCCCGAGAGAGCCAGGGCCATGGAGGCCAACATGCCGAAGCG CAAGAAGAGACCGAGGCGGGTGGCCCCGAGAGGGCCAGGGCCATGGAGGCCAACATGCCGAAGCG T C DNAJC27 Ensembl:ENSG00000115137 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24971863..24972048 26863196 MeRIP-seq:(Medium) rs780306898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_223761,Human_Splice_Rec_223771,Human_Splice_Rec_223783,Human_Splice_Rec_223823 88817 RMVar_ID_88817 Human_SNP_ID_64165999 m1A Human chr2 + 24971926 24971926 24971926 TTGGCCTCCATGGCCCTGGCTCTCTCGGGGCCACCCGCCTCGGTCTCTTCTTGTGCACCGCTGGC TTGGCCTCCATGGCCCTGGCTCTCTCGGGGCCCCCCGCCTCGGTCTCTTCTTGTGCACCGCTGGC A C DNAJC27-AS1 Ensembl:ENSG00000224165 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:24971439..24972263 26863196 MeRIP-seq:(Medium) rs749652378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5198567,Human_RBP_ID_27158813 88818 RMVar_ID_88818 Human_SNP_ID_64234928 m1A Human chr2 + 25248160 25248155 25248160 GATGCGGGGTCAGTGGGCTGCTGCACAGCAGGAGGGCTGGCCTCCTCCACCTTCTGAGACTCCCC GATGCGGGGTCAGTGGGCTGCTGCACAG_____GGGCTGGCCTCCTCCACCTTCTGAGACTCCCC GCAGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:25248111..25249696;chr2:25248115..25248228 26863196 MeRIP-seq:(Medium) rs1176181786 Functional Loss DEL dbSNP153 29..33 33 - - - 88819 RMVar_ID_88819 Human_SNP_ID_64238295 m1A Human chr2 - 25261792 25261792 25261792 AGAAAGCAGACCTGCTAGGAGAGGACCAGGATAGGGAGGGGCAGGGACAAGGACATGGGACTTCT AGAAAGCAGACCTGCTAGGAGAGGACCAGGATGGGGAGGGGCAGGGACAAGGACATGGGACTTCT T C DNMT3A Ensembl:ENSG00000119772 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:25261789..25261874 26863196 MeRIP-seq:(Medium) rs915925654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78910,RMVar_hsa_circ_125739,RMVar_hsa_circ_197700,RMVar_hsa_circ_197702,RMVar_hsa_circ_124690,RMVar_hsa_circ_197705,RMVar_hsa_circ_14564 88820 RMVar_ID_88820 Human_SNP_ID_64242030 m1A Human chr2 - 25277245 25277245 25277245 GGCTGTGGTGGGAGAGAGGACGGAAAGGAAACAGGGAGGCAGAGCCAGACAAGATGGGTGAGACA GGCTGTGGTGGGAGAGAGGACGGAAAGGAAACGGGGAGGCAGAGCCAGACAAGATGGGTGAGACA T C DNMT3A Ensembl:ENSG00000119772 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:25277230..25277316 26863196 MeRIP-seq:(Medium) rs181901417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639735 RMVar_hsa_circ_78910,RMVar_hsa_circ_125739,RMVar_hsa_circ_197700,RMVar_hsa_circ_197702,RMVar_hsa_circ_124690,RMVar_hsa_circ_197705,RMVar_hsa_circ_197708,RMVar_hsa_circ_284371,RMVar_hsa_circ_14564,RMVar_hsa_circ_284179,RMVar_hsa_circ_197707 88821 RMVar_ID_88821 Human_SNP_ID_64247697 m1A Human chr2 - 25300224 25300224 25300224 TCTGTGCCTGCAGGACGGAGAGGAGCAGGAGGAGCCGCGTGGCAAGGAGGAGCGCCAAGAGCCCA TCTGTGCCTGCAGGACGGAGAGGAGCAGGAGGCGCCGCGTGGCAAGGAGGAGCGCCAAGAGCCCA T G DNMT3A Ensembl:ENSG00000119772 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:25300174..25300279 26863196 MeRIP-seq:(Medium) rs747483936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_224104,Human_Splice_Rec_224105,Human_Splice_Rec_224182,Human_Splice_Rec_224183,Human_Splice_Rec_224224,Human_Splice_Rec_224225,Human_Splice_Rec_224374,Human_Splice_Rec_224375 RMVar_hsa_circ_78910,RMVar_hsa_circ_125739,RMVar_hsa_circ_197700,RMVar_hsa_circ_5165,RMVar_hsa_circ_197702,RMVar_hsa_circ_124690,RMVar_hsa_circ_197705,RMVar_hsa_circ_197708,RMVar_hsa_circ_14564,RMVar_hsa_circ_284179,RMVar_hsa_circ_288310,RMVar_hsa_circ_197709,RMVar_hsa_circ_365453 88822 RMVar_ID_88822 Human_SNP_ID_64251319 m1A Human chr2 + 25313969 25313969 25313969 AGCAGAGCTGCTGGTGTCCCCGGGGCCGCTGGAGGGCATGGCGGGCATCTGGGCGCCGGGAGGCA AGCAGAGCTGCTGGTGTCCCCGGGGCCGCTGGCGGGCATGGCGGGCATCTGGGCGCCGGGAGGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:25313883..25314019 26863196 MeRIP-seq:(Medium) rs773893946 Functional Loss SNV dbSNP153 33..33 33 - - - 88823 RMVar_ID_88823 Human_SNP_ID_64257509 m1A Human chr2 + 25339819 25339819 25339819 GCCTGGCCCCCCAAATCCCACAGGCCAGTCCTAACACCCAGGCAATAGCAAGGCGAATAGCTCCC GCCTGGCCCCCCAAATCCCACAGGCCAGTCCTGACACCCAGGCAATAGCAAGGCGAATAGCTCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:25339816..25339916 32194978 MeRIP-seq:(Medium) rs561897793 Functional Loss SNV dbSNP153 33..33 33 - - - 88824 RMVar_ID_88824 Human_SNP_ID_64258426 m1A Human chr2 + 25342411 25342411 25342411 GCCGAGCTCCGGGCCTCGCCGCAGCCCTCCCCACGCTGGGCGCCCCGCTACCTGGCGCTGCTTCT GCCGAGCTCCGGGCCTCGCCGCAGCCCTCCCCGCGCTGGGCGCCCCGCTACCTGGCGCTGCTTCT A G lnc-EFR3B-7,lnc-EFR3B-7:2 RNACentral:URS0000D59B83,RNACentral:URS0000D5C817 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:25342404..25342487 26863196 MeRIP-seq:(Medium) rs1178570038 Functional Loss SNV dbSNP153 33..33 33 - - - 88825 RMVar_ID_88825 Human_SNP_ID_64279230 m1A Human chr2 - 25425511 25425511 25425511 GGAGACTAATTTCATCCTCCAGGCCCGAAGTGACAAGGATCTTAACCCCAGGAGTGGTAGCCCAG GGAGACTAATTTCATCCTCCAGGCCCGAAGTGGCAAGGATCTTAACCCCAGGAGTGGTAGCCCAG T C DTNB Ensembl:ENSG00000138101 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:25425509..25425583 26863196 MeRIP-seq:(Medium) rs866178680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56102,RMVar_hsa_circ_197710,RMVar_hsa_circ_127796,RMVar_hsa_circ_119825,RMVar_hsa_circ_197711 88826 RMVar_ID_88826 Human_SNP_ID_64313455 m1A Human chr2 - 25570677 25570677 25570677 GATGAAAGCCAGGAGAGTGTGTGTTCTGGAAAACAAGTGAAGAATGTGTTTTGAGGAGGAGGAAG GATGAAAGCCAGGAGAGTGTGTGTTCTGGAAAGCAAGTGAAGAATGTGTTTTGAGGAGGAGGAAG T C DTNB Ensembl:ENSG00000138101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:25570600..25570701 26863196 MeRIP-seq:(Medium) rs1382443132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109977,RMVar_hsa_circ_197720,RMVar_hsa_circ_71738,RMVar_hsa_circ_197718,RMVar_hsa_circ_54751,RMVar_hsa_circ_339329,RMVar_hsa_circ_350352,RMVar_hsa_circ_350939,RMVar_hsa_circ_349481,RMVar_hsa_circ_326388,RMVar_hsa_circ_197722,RMVar_hsa_circ_197723,RMVar_hsa_circ_197721 88827 RMVar_ID_88827 Human_SNP_ID_64355847 m1A Human chr2 + 25743936 25743936 25743936 TGCTCTGGTGGGGTTCAGTTTTTCATTATCCAATTTCTCTATGTGGGCTGGTGATGGGACACTTG TGCTCTGGTGGGGTTCAGTTTTTCATTATCCAGTTTCTCTATGTGGGCTGGTGATGGGACACTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:25743888..25744045 26863196 MeRIP-seq:(Medium) rs750828218 Functional Loss SNV dbSNP153 33..33 33 - - - 88828 RMVar_ID_88828 Human_SNP_ID_64389008 m1A Human chr2 - 25878256 25878256 25878256 CAGAGCAGGCAGGGAGGGCGGCCGGAGCCCGGACACGGGAGCCTCCCAGTCAGTTCAAGACCCGA CAGAGCAGGCAGGGAGGGCGGCCGGAGCCCGGGCACGGGAGCCTCCCAGTCAGTTCAAGACCCGA T C ASXL2 Ensembl:ENSG00000143970 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:25878206..25878450 26863196 MeRIP-seq:(Medium) rs1559535752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_224861,Human_Splice_Rec_224885 88829 RMVar_ID_88829 Human_SNP_ID_64415145 m1A Human chr2 - 25980597 25980594 25980597 GGGTGGCAGAAGAGGAGGATGACAACAACAACAACCACCGCCCGCCCCAGCCCATCCTGGAGTCA GGGTGGCAGAAGAGGAGGATGACAACAACAAC___CACCGCCCGCCCCAGCCCATCCTGGAGTCA GGTT G KIF3C Ensembl:ENSG00000084731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:25980400..25980948 26863196 MeRIP-seq:(Medium) rs779696548 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_915325 88830 RMVar_ID_88830 Human_SNP_ID_64415148 m1A Human chr2 - 25980597 25980597 25980597 GGGTGGCAGAAGAGGAGGATGACAACAACAACAACCACCGCCCGCCCCAGCCCATCCTGGAGTCA GGGTGGCAGAAGAGGAGGATGACAACAACAACCACCACCGCCCGCCCCAGCCCATCCTGGAGTCA T G KIF3C Ensembl:ENSG00000084731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:25980400..25980948 26863196 MeRIP-seq:(Medium) rs760130546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915325 88831 RMVar_ID_88831 Human_SNP_ID_64415183 m1A Human chr2 + 25980674 25980674 25980674 CTGGGCCCTCAGGGTACCCAGGCGGGGCGGACACGGCCTTCTTCCTGCGGCTGCTCTTCCTCCGG CTGGGCCCTCAGGGTACCCAGGCGGGGCGGACGCGGCCTTCTTCCTGCGGCTGCTCTTCCTCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:25980627..25980796 26863196 MeRIP-seq:(Medium) rs1553717735 Functional Loss SNV dbSNP153 33..33 33 - - - 88832 RMVar_ID_88832 Human_SNP_ID_64415497 m1A Human chr2 - 25981608 25981608 25981608 TGTTTGCCTATGGCCAGACGGGCACTGGCAAGACCTATACCATGCAGGGGACCTGGGTGGAGCCC TGTTTGCCTATGGCCAGACGGGCACTGGCAAGTCCTATACCATGCAGGGGACCTGGGTGGAGCCC T A KIF3C Ensembl:ENSG00000084731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:25981557..25982203 32194978 MeRIP-seq:(Medium) rs112801727 Functional Loss SNV dbSNP153 33..33 33 - - - 88833 RMVar_ID_88833 Human_SNP_ID_64415498 m1A Human chr2 - 25981608 25981608 25981608 TGTTTGCCTATGGCCAGACGGGCACTGGCAAGACCTATACCATGCAGGGGACCTGGGTGGAGCCC TGTTTGCCTATGGCCAGACGGGCACTGGCAAGGCCTATACCATGCAGGGGACCTGGGTGGAGCCC T C KIF3C Ensembl:ENSG00000084731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:25981557..25982203 32194978 MeRIP-seq:(Medium) rs112801727 Functional Loss SNV dbSNP153 33..33 33 - - - 88834 RMVar_ID_88834 Human_SNP_ID_64468885 m1A Human chr2 + 26184345 26184345 26184345 CCAGGCGGAGATCCTGTGCGCCAAGACCACCAAGGAGCGCTCGCGCTTCACCACCCTCCTGCGAA CCAGGCGGAGATCCTGTGCGCCAAGACCACCAGGGAGCGCTCGCGCTTCACCACCCTCCTGCGAA A G GAREM2 Ensembl:ENSG00000157833 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:26184294..26184489 26863196 MeRIP-seq:(Medium) rs373713812 Functional Loss SNV dbSNP153 33..33 33 - - - 88835 RMVar_ID_88835 Human_SNP_ID_64469842 m1A Human chr2 + 26187398 26187398 26187398 ACAGCCCAGCCAGGCCTCCCGGGCCCTCACAGAGCCTCTGAGCGGTCGAGCCGCCTCCCTTCTGG ACAGCCCAGCCAGGCCTCCCGGGCCCTCACAGTGCCTCTGAGCGGTCGAGCCGCCTCCCTTCTGG A T GAREM2 Ensembl:ENSG00000157833 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:26187350..26187424 26863196 MeRIP-seq:(Medium) rs1476961979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17392560 88836 RMVar_ID_88836 Human_SNP_ID_64469914 m1A Human chr2 + 26187561 26187561 26187561 TTTTCCGGGCCTGCCTACCCCTCAGGCCCTTCAGCGGCCTTGTCTTCTGGGCCCAGAACCACCTC TTTTCCGGGCCTGCCTACCCCTCAGGCCCTTCGGCGGCCTTGTCTTCTGGGCCCAGAACCACCTC A G GAREM2 Ensembl:ENSG00000157833 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:26187516..26187617 32194978 MeRIP-seq:(Medium) rs773179492 Functional Loss SNV dbSNP153 33..33 33 - - - 88837 RMVar_ID_88837 Human_SNP_ID_64470886 m1A Human chr2 + 26191087 26191087 26191087 TGCAAACTAATTCGAAGTCACACTTCACCAGGAGGGAGAGATGGTCTTGGCTGAAGGCACTTTAA TGCAAACTAATTCGAAGTCACACTTCACCAGGTGGGAGAGATGGTCTTGGCTGAAGGCACTTTAA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:26191076..26191100 26863196 MeRIP-seq:(Medium) rs1024570381 Functional Loss SNV dbSNP153 33..33 33 - - - 88838 RMVar_ID_88838 Human_SNP_ID_64474329 m1A Human chr2 + 26204119 26204119 26204119 GGTCTAGCGCAGTGAGGGTGGCATCTTTAAGTATAGTCTTTAGCCCCTTATCCACGGAGACTTGG GGTCTAGCGCAGTGAGGGTGGCATCTTTAAGTGTAGTCTTTAGCCCCTTATCCACGGAGACTTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:26204068..26209850 32194978 MeRIP-seq:(Medium) rs773829713 Functional Loss SNV dbSNP153 33..33 33 - - - 88839 RMVar_ID_88839 Human_SNP_ID_64479818 m1A Human chr2 + 26230266 26230266 26230266 CCCTGTCTGCACGAATGCTTCTACCAGTCAGCATCATGTCCAAAGCAGCAGGCACACCCACCTAA CCCTGTCTGCACGAATGCTTCTACCAGTCAGCGTCATGTCCAAAGCAGCAGGCACACCCACCTAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:26230152..26230290 26863196 MeRIP-seq:(Medium) rs867272687 Functional Loss SNV dbSNP153 33..33 33 - - - 88840 RMVar_ID_88840 Human_SNP_ID_64483406 m1A Human chr2 + 26244988 26244988 26244988 GCTCCGAGAGGGAGTCCTCGCGGACGTCAGCCAAGGTGAGACGGCGAGCCCTCAGCTCTCCGCCC GCTCCGAGAGGGAGTCCTCGCGGACGTCAGCCGAGGTGAGACGGCGAGCCCTCAGCTCTCCGCCC A G HADHB Ensembl:ENSG00000138029 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:26244946..26245046;chr2:26244956..26245042 26863196 MeRIP-seq:(Medium) rs1012719947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1096902,Human_RBP_ID_4623163,Human_RBP_ID_17277498,Human_RBP_ID_17392574,Human_RBP_ID_18421718,Human_RBP_ID_19097046,Human_RBP_ID_22076159,Human_RBP_ID_22359887 Human_Splice_Rec_225443,Human_Splice_Rec_225471,Human_Splice_Rec_225475,Human_Splice_Rec_225501 88841 RMVar_ID_88841 Human_SNP_ID_64491842 m1A Human chr2 - 26279220 26279220 26279220 TGTGAGAGCGCAGTGCATATTCATCCTGTTCCAGCCGAGAAACAGCAAAGGCAGCGGCCAGTCGG TGTGAGAGCGCAGTGCATATTCATCCTGTTCCGGCCGAGAAACAGCAAAGGCAGCGGCCAGTCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:26279170..26279251 26863196 MeRIP-seq:(Medium) rs140128759 Functional Loss SNV dbSNP153 33..33 33 - - - 88842 RMVar_ID_88842 Human_SNP_ID_64606819 m1A Human chr2 - 26724907 26724907 26724907 CCAGAGACCCGTCCTTAGCCCACACCCAGCCAAGCCGGCCCCTCCTCTCCACAGTGCTTCCCACA CCAGAGACCCGTCCTTAGCCCACACCCAGCCAGGCCGGCCCCTCCTCTCCACAGTGCTTCCCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:26724857..26724940 26863196 MeRIP-seq:(Medium) rs1490763729 Functional Loss SNV dbSNP153 33..33 33 - - - 88843 RMVar_ID_88843 Human_SNP_ID_64616832 m1A Human chr2 + 26764337 26764337 26764337 GGGGCCCGGCGCCGCTAACTGGAGCGAACCCCAGCGTCCGCCGACATGGCCTGGACCAAGTACCA GGGGCCCGGCGCCGCTAACTGGAGCGAACCCCGGCGTCCGCCGACATGGCCTGGACCAAGTACCA A G CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:26764307..26764400 26863410 MeRIP-seq:(Medium) rs1342316464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622283 Human_Splice_Rec_226369,Human_Splice_Rec_226377,Human_Splice_Rec_226387,Human_Splice_Rec_226391,Human_Splice_Rec_226399 88844 RMVar_ID_88844 Human_SNP_ID_64622422 m1A Human chr2 + 26786152 26786152 26786152 GCCAGCCTTTCGCTCCCGGACCCGGCAGCCCGAGCAGGAGCCGTGGGACCGGGCGCCAGCACCCT GCCAGCCTTTCGCTCCCGGACCCGGCAGCCCGCGCAGGAGCCGTGGGACCGGGCGCCAGCACCCT A C CENPA Ensembl:ENSG00000115163 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:26786007..26786156 32194978 MeRIP-seq:(Medium) rs758437466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623165,Human_RBP_ID_22076163 88845 RMVar_ID_88845 Human_SNP_ID_64622463 m1A Human chr2 + 26786263 26786263 26786263 CCCCGAGGAGGCGCAGCCCGAGCCCGACCCCGACCCCCGGCCCCTCCCGGCGGGGCCCCTCCTTA CCCCGAGGAGGCGCAGCCCGAGCCCGACCCCGGCCCCCGGCCCCTCCCGGCGGGGCCCCTCCTTA A G CENPA Ensembl:ENSG00000115163 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:26786106..26792188 26863410 MeRIP-seq:(Medium) rs1451261490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_226413,Human_Splice_Rec_226421,Human_Splice_Rec_226427,Human_Splice_Rec_226435 88846 RMVar_ID_88846 Human_SNP_ID_64622474 m1A Human chr2 - 26786294 26786291 26786294 CCTCTTCGAGATGGGGCCGCGGCCGGTTACCTAAGGAGGGGCCCCGCCGGGAGGGGCCGGGGGTC CCTCTTCGAGATGGGGCCGCGGCCGGTTACCT___GAGGGGCCCCGCCGGGAGGGGCCGGGGGTC CCTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:26786254..26792549 32194978 MeRIP-seq:(Medium) rs1411487157 Functional Loss DEL dbSNP153 33..35 33 - - - 88847 RMVar_ID_88847 Human_SNP_ID_64639842 m1A Human chr2 + 26848179 26848179 26848179 CGAGCGCGCGTGCAGCCGCCGCCGCCCCGAGCACCCGCAGCTCCGGCGCCGCGGCGAGACGGAGA CGAGCGCGCGTGCAGCCGCCGCCGCCCCGAGCCCCCGCAGCTCCGGCGCCGCGGCGAGACGGAGA A C DPYSL5 Ensembl:ENSG00000157851 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:26848081..26848275 26863410 MeRIP-seq:(Medium) rs888278027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_226451 88848 RMVar_ID_88848 Human_SNP_ID_64668553 m1A Human chr2 + 26970757 26970757 26970757 GGAGCCGCAGCCTCTGCCGCAGCGCCCCCGCCACCTGTCCCCTCCCCCTCCGCCTCCGCCGGAGC GGAGCCGCAGCCTCTGCCGCAGCGCCCCCGCCCCCTGTCCCCTCCCCCTCCGCCTCCGCCGGAGC A C MAPRE3 Ensembl:ENSG00000084764 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:26970675..26970800 26863410 MeRIP-seq:(Medium) rs1375594196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548438,Human_RBP_ID_4604799,Human_RBP_ID_5322430,Human_RBP_ID_17392577,Human_RBP_ID_22533566 Human_Splice_Rec_226539,Human_Splice_Rec_226541,Human_Splice_Rec_226553,Human_Splice_Rec_226565 88849 RMVar_ID_88849 Human_SNP_ID_64680463 m1A Human chr2 + 27026377 27026377 27026377 CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACAGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACCGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC A C MAPRE3 Ensembl:ENSG00000084764 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3754733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27816894 Human_Splice_Rec_226552,Human_Splice_Rec_226564,Human_Splice_Rec_226590,Human_Splice_Rec_226616 GWAS_ID_11541,GWAS_ID_11542,GWAS_ID_11543,GWAS_ID_11544,GWAS_ID_11545,GWAS_ID_11546,GWAS_ID_11547,GWAS_ID_11548,GWAS_ID_11549,GWAS_ID_11550,GWAS_ID_11551,GWAS_ID_11552,GWAS_ID_11553,GWAS_ID_11554,GWAS_ID_11555,GWAS_ID_11556,GWAS_ID_11557,GWAS_ID_11558,GWAS_ID_11559,GWAS_ID_11560,GWAS_ID_11561 88850 RMVar_ID_88850 Human_SNP_ID_64680464 m1A Human chr2 + 27026377 27026377 27026377 CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACAGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACGGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC A G MAPRE3 Ensembl:ENSG00000084764 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3754733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27816894 Human_Splice_Rec_226552,Human_Splice_Rec_226564,Human_Splice_Rec_226590,Human_Splice_Rec_226616 GWAS_ID_11541,GWAS_ID_11542,GWAS_ID_11543,GWAS_ID_11544,GWAS_ID_11545,GWAS_ID_11546,GWAS_ID_11547,GWAS_ID_11548,GWAS_ID_11549,GWAS_ID_11550,GWAS_ID_11551,GWAS_ID_11552,GWAS_ID_11553,GWAS_ID_11554,GWAS_ID_11555,GWAS_ID_11556,GWAS_ID_11557,GWAS_ID_11558,GWAS_ID_11559,GWAS_ID_11560,GWAS_ID_11561 88851 RMVar_ID_88851 Human_SNP_ID_64680603 m1A Human chr2 + 27026963 27026963 27026963 CAGGGAAAGGGAGGGGGGCATGTGAGGGATGGAAATGACCTCCTGGCACCAGGCTCACCCACCCA CAGGGAAAGGGAGGGGGGCATGTGAGGGATGGGAATGACCTCCTGGCACCAGGCTCACCCACCCA A G MAPRE3 Ensembl:ENSG00000084764 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27026912..27027004 26863196 MeRIP-seq:(Medium) rs957809422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264183,Human_RBP_ID_3957655,Human_RBP_ID_4604832,Human_RBP_ID_5118252,Human_RBP_ID_5146517,Human_RBP_ID_5322033,Human_RBP_ID_9105132,Human_RBP_ID_9429206,Human_RBP_ID_17954727,Human_RBP_ID_26486287 88852 RMVar_ID_88852 Human_SNP_ID_64681978 m1A Human chr2 + 27033025 27033025 27033025 CCGAGGAGGGAGGGCTGCGAGCCATGGCGACCAAGACGGCGGGCGTGGGGCGGTGGGAGGTAGTG CCGAGGAGGGAGGGCTGCGAGCCATGGCGACCGAGACGGCGGGCGTGGGGCGGTGGGAGGTAGTG A G TMEM214 Ensembl:ENSG00000119777 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:27032951..27034171;chr2:27032976..27033150;chr2:27032926..27034204;chr2:27032926..27034225;chr2:27032950..27033224;chr2:27032976..27033175 26863196 MeRIP-seq:(Medium) rs1056658474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828571,Human_RBP_ID_4622287,Human_RBP_ID_5146519,Human_RBP_ID_8851795,Human_RBP_ID_9428603,Human_RBP_ID_18421720,Human_RBP_ID_22597770 RMVar_hsa_circ_123128,RMVar_hsa_circ_197839 88853 RMVar_ID_88853 Human_SNP_ID_64681979 m1A Human chr2 + 27033026 27033026 27033026 CGAGGAGGGAGGGCTGCGAGCCATGGCGACCAAGACGGCGGGCGTGGGGCGGTGGGAGGTAGTGA CGAGGAGGGAGGGCTGCGAGCCATGGCGACCAGGACGGCGGGCGTGGGGCGGTGGGAGGTAGTGA A G TMEM214 Ensembl:ENSG00000119777 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27032976..27033175 26863196 MeRIP-seq:(Medium) rs1164627438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828571,Human_RBP_ID_4622287,Human_RBP_ID_5146519,Human_RBP_ID_8851795,Human_RBP_ID_9428603,Human_RBP_ID_18421720,Human_RBP_ID_22597770 RMVar_hsa_circ_123128,RMVar_hsa_circ_197839 88854 RMVar_ID_88854 Human_SNP_ID_64682706 m1A Human chr2 + 27035661 27035661 27035661 GGGATCATCCGAGGGCTGCTGGCGAAGGCAGCAGGGTCTCTGGAGCTCTTTTTTGACCACTGTCT GGGATCATCCGAGGGCTGCTGGCGAAGGCAGCGGGGTCTCTGGAGCTCTTTTTTGACCACTGTCT A G TMEM214 Ensembl:ENSG00000119777 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27035612..27035712 32194978 MeRIP-seq:(Medium) rs1464103246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9386165,Human_RBP_ID_17965891,Human_RBP_ID_18470765,Human_RBP_ID_22996794 Human_Splice_Rec_226650,Human_Splice_Rec_226651,Human_Splice_Rec_226682,Human_Splice_Rec_226683,Human_Splice_Rec_226712,Human_Splice_Rec_226713 Human_miRNA_ID_1987598,Human_miRNA_ID_2510644,Human_miRNA_ID_2823820,Human_miRNA_ID_2857791,Human_miRNA_ID_3053465 RMVar_hsa_circ_123128,RMVar_hsa_circ_89690,RMVar_hsa_circ_315911,RMVar_hsa_circ_197839,RMVar_hsa_circ_107517,RMVar_hsa_circ_40928,RMVar_hsa_circ_61860,RMVar_hsa_circ_197841,RMVar_hsa_circ_197842,RMVar_hsa_circ_197840,RMVar_hsa_circ_76788,RMVar_hsa_circ_94383,RMVar_hsa_circ_197846,RMVar_hsa_circ_72976,RMVar_hsa_circ_197845,RMVar_hsa_circ_113408,RMVar_hsa_circ_197847 88855 RMVar_ID_88855 Human_SNP_ID_64684244 m1A Human chr2 - 27040438 27040438 27040438 GGCCCAGGCCAGGGCCTCAAGCAAGAGGTGCCACAGTGGCAGCAGCACATTCTGGTGGAAAAGCA GGCCCAGGCCAGGGCCTCAAGCAAGAGGTGCCGCAGTGGCAGCAGCACATTCTGGTGGAAAAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27040389..27040902 32194978 MeRIP-seq:(Medium) rs201363309 Functional Loss SNV dbSNP153 33..33 33 - - - 88856 RMVar_ID_88856 Human_SNP_ID_64684442 m1A Human chr2 - 27041052 27041052 27041052 GAGGCTGGGGGCCATGTGCAGTAGGGCCAGAAAAGTGTTCAGTGGAATTGTGGGTAGGAGGCTGA GAGGCTGGGGGCCATGTGCAGTAGGGCCAGAACAGTGTTCAGTGGAATTGTGGGTAGGAGGCTGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27041002..27041204 26863196 MeRIP-seq:(Medium) rs937034823 Functional Loss SNV dbSNP153 33..33 33 - - - 88857 RMVar_ID_88857 Human_SNP_ID_64687102 m1A Human chr2 + 27050834 27050834 27050834 AGAGCGGAGGACTGTAGTGGATAGGGCGTGGCAATCCTTAGGTCGCTGGTTCGATTCCGGCTCGA AGAGCGGAGGACTGTAGTGGATAGGGCGTGGCGATCCTTAGGTCGCTGGTTCGATTCCGGCTCGA A G AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:27050776..27050911 26863196 MeRIP-seq:(Medium) rs1039176747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55678,Human_RBP_ID_142025,Human_RBP_ID_243416,Human_RBP_ID_270216,Human_RBP_ID_280821,Human_RBP_ID_548490,Human_RBP_ID_777931,Human_RBP_ID_828071,Human_RBP_ID_1022790,Human_RBP_ID_1195625,Human_RBP_ID_1241049,Human_RBP_ID_1300515,Human_RBP_ID_1377810,Human_RBP_ID_1585508,Human_RBP_ID_1914758,Human_RBP_ID_2634723,Human_RBP_ID_3621733,Human_RBP_ID_4631907,Human_RBP_ID_5194563,Human_RBP_ID_5422970,Human_RBP_ID_5445342,Human_RBP_ID_5470693,Human_RBP_ID_5502047,Human_RBP_ID_5536117,Human_RBP_ID_6905824,Human_RBP_ID_8107905,Human_RBP_ID_8257565,Human_RBP_ID_8516546,Human_RBP_ID_8847418,Human_RBP_ID_9105134,Human_RBP_ID_9979563,Human_RBP_ID_13840186,Human_RBP_ID_17015489,Human_RBP_ID_17207673,Human_RBP_ID_17507027,Human_RBP_ID_17698895,Human_RBP_ID_17954737,Human_RBP_ID_18200900,Human_RBP_ID_18209218,Human_RBP_ID_18316156,Human_RBP_ID_18409494,Human_RBP_ID_18515642,Human_RBP_ID_18758254,Human_RBP_ID_20558859,Human_RBP_ID_22074579,Human_RBP_ID_22250227,Human_RBP_ID_22393396,Human_RBP_ID_22422718,Human_RBP_ID_22815300,Human_RBP_ID_22991392,Human_RBP_ID_23132910,Human_RBP_ID_23182551,Human_RBP_ID_23281505,Human_RBP_ID_23865156,Human_RBP_ID_24423882,Human_RBP_ID_25529856,Human_RBP_ID_26487756,Human_RBP_ID_26664900,Human_RBP_ID_26750101,Human_RBP_ID_27010158,Human_RBP_ID_27289107,Human_RBP_ID_27479328,Human_RBP_ID_27694657 88858 RMVar_ID_88858 Human_SNP_ID_64687686 m1A Human chr2 - 27051730 27051730 27051730 CCCGCTAGCGAGGCCGCACCTTGGGCCCCGGCACCCGGGCCCTCCACCCGGGCCCCCAAAAACAC CCCGCTAGCGAGGCCGCACCTTGGGCCCCGGCGCCCGGGCCCTCCACCCGGGCCCCCAAAAACAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:27051651..27052020;chr2:27051651..27051915;chr2:27051651..27051965 26863196 MeRIP-seq:(Medium) rs750110766 Functional Loss SNV dbSNP153 33..33 33 - - - 88859 RMVar_ID_88859 Human_SNP_ID_64687707 m1A Human chr2 + 27051778 27051778 27051778 GCGGCCTCGCTAGCGGGAGAGGGAGCGGGATCACCGGCCCGGAGAGAGGTGAGGGGCTCTGCGCG GCGGCCTCGCTAGCGGGAGAGGGAGCGGGATCTCCGGCCCGGAGAGAGGTGAGGGGCTCTGCGCG A T AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:27051676..27051843 26863410 MeRIP-seq:(Medium) rs913566108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4604892,Human_RBP_ID_5527448,Human_RBP_ID_17658395 Human_Splice_Rec_226831,Human_Splice_Rec_226861,Human_Splice_Rec_226865,Human_Splice_Rec_226879,Human_Splice_Rec_226907,Human_Splice_Rec_226927 RMVar_hsa_circ_24376 88860 RMVar_ID_88860 Human_SNP_ID_64688772 m1A Human chr2 + 27055250 27055250 27055250 GTTGAACCCCGATGGTGTGGTCCGGGGACACTACCGGTAAGTGGCTTCCCCAGCCTGTCTGGACT GTTGAACCCCGATGGTGTGGTCCGGGGACACTGCCGGTAAGTGGCTTCCCCAGCCTGTCTGGACT A G AGBL5 Ensembl:ENSG00000084693 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27054660..27055277 32194978 MeRIP-seq:(Medium) rs1357953243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920491,Human_RBP_ID_19001297,Human_RBP_ID_19099597 Human_Splice_Rec_226841,Human_Splice_Rec_226889,Human_Splice_Rec_226917,Human_Splice_Rec_226937 RMVar_hsa_circ_24376,RMVar_hsa_circ_84980,RMVar_hsa_circ_197868,RMVar_hsa_circ_54257,RMVar_hsa_circ_115316,RMVar_hsa_circ_94549,RMVar_hsa_circ_197869,RMVar_hsa_circ_197870 88861 RMVar_ID_88861 Human_SNP_ID_64688948 m1A Human chr2 + 27055879 27055879 27055879 TGATGCTCCTGTTTCTGACCTGGAGAAAGCCAACAATCTCCAAAATGAAGCTCAGTGTGGGCACT TGATGCTCCTGTTTCTGACCTGGAGAAAGCCAGCAATCTCCAAAATGAAGCTCAGTGTGGGCACT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs766582593 Functional Loss SNV dbSNP153 33..33 33 - - - 88862 RMVar_ID_88862 Human_SNP_ID_64689196 m1A Human chr2 + 27056705 27056705 27056705 CGACTTCCAGGGCTGCAATTTCTCAGAGAAGAATATGTATGCCCGAGACCGTAGAGATGGCCAGT CGACTTCCAGGGCTGCAATTTCTCAGAGAAGAGTATGTATGCCCGAGACCGTAGAGATGGCCAGT A G AGBL5 Ensembl:ENSG00000084693 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27056654..27056755 32194978 MeRIP-seq:(Medium) rs770469630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1914769,Human_RBP_ID_26819575 Human_Splice_Rec_226844,Human_Splice_Rec_226845,Human_Splice_Rec_226878,Human_Splice_Rec_226892,Human_Splice_Rec_226893,Human_Splice_Rec_226920,Human_Splice_Rec_226921 RMVar_hsa_circ_24376,RMVar_hsa_circ_84980,RMVar_hsa_circ_197868,RMVar_hsa_circ_54257,RMVar_hsa_circ_128019,RMVar_hsa_circ_115316,RMVar_hsa_circ_94549,RMVar_hsa_circ_197869,RMVar_hsa_circ_197870,RMVar_hsa_circ_197871 88863 RMVar_ID_88863 Human_SNP_ID_64692625 m1A Human chr2 + 27068932 27068932 27068932 CAGTCCCCTTCCTGCCCTCCACCATCCCCATCAGCCAGGTCATTTGCTTGCTTTCAACCTGTGTC CAGTCCCCTTCCTGCCCTCCACCATCCCCATCGGCCAGGTCATTTGCTTGCTTTCAACCTGTGTC A G AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27068906..27069012 26863196 MeRIP-seq:(Medium) rs1187274142 Functional Loss SNV dbSNP153 33..33 33 - - - 88864 RMVar_ID_88864 Human_SNP_ID_64693201 m1A Human chr2 + 27070676 27070676 27070676 GTGATGGGTAGAAGGGATGAAGTGAAGTGTGAAGGCCCCTCATACCCTCCATCTTGCCTCAGACT GTGATGGGTAGAAGGGATGAAGTGAAGTGTGAGGGCCCCTCATACCCTCCATCTTGCCTCAGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27070558..27070739 26863196 MeRIP-seq:(Medium) rs556530355 Functional Loss SNV dbSNP153 33..33 33 - - - 88865 RMVar_ID_88865 Human_SNP_ID_64693422 m1A Human chr2 - 27071426 27071426 27071426 TCACGGACGTGCAGCTCGCCATCTTCGCCAACATGCTGGGCGTGTCGCTCTTCTTGCTTGTCGTT TCACGGACGTGCAGCTCGCCATCTTCGCCAACGTGCTGGGCGTGTCGCTCTTCTTGCTTGTCGTT T C OST4 Ensembl:ENSG00000228474 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27071376..27071475 32194978 MeRIP-seq:(Medium) rs950544773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548550,Human_RBP_ID_776739,Human_RBP_ID_1585518,Human_RBP_ID_4604997,Human_RBP_ID_5322435,Human_RBP_ID_9105142,Human_RBP_ID_9330960,Human_RBP_ID_19097079,Human_RBP_ID_23865188,Human_RBP_ID_27010184 Human_Splice_Rec_226946,Human_Splice_Rec_226950 Human_miRNA_ID_2440316 RMVar_hsa_circ_82670,RMVar_hsa_circ_197876,RMVar_hsa_circ_197877 88866 RMVar_ID_88866 Human_SNP_ID_64693434 m1A Human chr2 - 27071456 27071456 27071456 AGCTCAGCCCCTCTCTTCTCCGCAGGATGATCACGGACGTGCAGCTCGCCATCTTCGCCAACATG AGCTCAGCCCCTCTCTTCTCCGCAGGATGATCGCGGACGTGCAGCTCGCCATCTTCGCCAACATG T C OST4 Ensembl:ENSG00000228474 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:27071426..27071650 26863196 MeRIP-seq:(Medium) rs1409992710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548550,Human_RBP_ID_776740,Human_RBP_ID_917684,Human_RBP_ID_1585518,Human_RBP_ID_4622289,Human_RBP_ID_5322034,Human_RBP_ID_5470700,Human_RBP_ID_9105142,Human_RBP_ID_19097079 Human_Splice_Rec_226946,Human_Splice_Rec_226950 RMVar_hsa_circ_82670,RMVar_hsa_circ_197876,RMVar_hsa_circ_197877 88867 RMVar_ID_88867 Human_SNP_ID_64693437 m1A Human chr2 - 27071465 27071465 27071465 CCAGCCCGCAGCTCAGCCCCTCTCTTCTCCGCAGGATGATCACGGACGTGCAGCTCGCCATCTTC CCAGCCCGCAGCTCAGCCCCTCTCTTCTCCGCGGGATGATCACGGACGTGCAGCTCGCCATCTTC T C OST4 Ensembl:ENSG00000228474 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:27071376..27071587 26863410 MeRIP-seq:(Medium) rs777772420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_917684,Human_RBP_ID_19099598 RMVar_hsa_circ_197877 88868 RMVar_ID_88868 Human_SNP_ID_64700787 m1A Human chr2 + 27097552 27097552 27097552 GCAGGTGAAGATGCTGCAGCGGATAGACGCACACAACACCAGGCAGCCTCCAGAGCAGAAGATCC GCAGGTGAAGATGCTGCAGCGGATAGACGCACTCAACACCAGGCAGCCTCCAGAGCAGAAGATCC A T KHK Ensembl:ENSG00000138030 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27097502..27097567 26863196 MeRIP-seq:(Medium) rs748064599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9383317 Human_Splice_Rec_226982,Human_Splice_Rec_226983,Human_Splice_Rec_226996,Human_Splice_Rec_226997,Human_Splice_Rec_227014,Human_Splice_Rec_227015,Human_Splice_Rec_227030,Human_Splice_Rec_227031,Human_Splice_Rec_227038,Human_Splice_Rec_227042,Human_Splice_Rec_227043 Human_miRNA_ID_1768261,Human_miRNA_ID_2205704,Human_miRNA_ID_2712494,Human_miRNA_ID_3048476 RMVar_hsa_circ_305375,RMVar_hsa_circ_80157,RMVar_hsa_circ_197880,RMVar_hsa_circ_22788,RMVar_hsa_circ_197881 88869 RMVar_ID_88869 Human_SNP_ID_64701292 m1A Human chr2 + 27099280 27099280 27099280 AAGCCTTGAGGGGCTTGTATGGTCGTGTGAGGAAAGGGTGAGCCGGGGAAGCCAGGAAGGGGCTT AAGCCTTGAGGGGCTTGTATGGTCGTGTGAGGGAAGGGTGAGCCGGGGAAGCCAGGAAGGGGCTT A G KHK Ensembl:ENSG00000138030 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27096772..27099736 32194978 MeRIP-seq:(Medium) rs1464106813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548558,Human_RBP_ID_9386175,Human_RBP_ID_18999082 Human_Splice_Rec_226984,Human_Splice_Rec_226985,Human_Splice_Rec_226998,Human_Splice_Rec_226999,Human_Splice_Rec_227016,Human_Splice_Rec_227017,Human_Splice_Rec_227032,Human_Splice_Rec_227033,Human_Splice_Rec_227044,Human_Splice_Rec_227045 RMVar_hsa_circ_80157,RMVar_hsa_circ_22788,RMVar_hsa_circ_197881 88870 RMVar_ID_88870 Human_SNP_ID_64702269 m1A Human chr2 - 27101718 27101718 27101718 CAGGAGCCACAAGCTGTTGGAAGGCAGTCCCTATTAGCTAAAAGCCCATTAAGACAAGAAACACA CAGGAGCCACAAGCTGTTGGAAGGCAGTCCCTGTTAGCTAAAAGCCCATTAAGACAAGAAACACA T C CGREF1 Ensembl:ENSG00000138028 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27101667..27101799 26863196 MeRIP-seq:(Medium) rs760346863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17954776 88871 RMVar_ID_88871 Human_SNP_ID_64702463 m1A Human chr2 - 27102116 27102116 27102116 GTTGACAGCTGCTCTGGCCCCTGGAGCTGCCAACTCTCCTACCACCAACCCGGTAAGCTCTGCTG GTTGACAGCTGCTCTGGCCCCTGGAGCTGCCAGCTCTCCTACCACCAACCCGGTAAGCTCTGCTG T C CGREF1 Ensembl:ENSG00000138028 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27102099..27102170 26863196 MeRIP-seq:(Medium) rs944324710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_227067,Human_Splice_Rec_227069,Human_Splice_Rec_227081,Human_Splice_Rec_227091,Human_Splice_Rec_227101,Human_Splice_Rec_227113,Human_Splice_Rec_227121 88872 RMVar_ID_88872 Human_SNP_ID_64702589 m1A Human chr2 - 27102432 27102431 27102432 CCTCTCCCGGGCTGATTCTCCACTTTTCTGACAGACTTCTGCAGAGCTACCTAAAGGGACTAGGA CCTCTCCCGGGCTGATTCTCCACTTTTCTGAC_GACTTCTGCAGAGCTACCTAAAGGGACTAGGA CT C CGREF1 Ensembl:ENSG00000138028 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27102417..27102509 26863196 MeRIP-seq:(Medium) rs761907287 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_227065,Human_Splice_Rec_227079,Human_Splice_Rec_227089,Human_Splice_Rec_227099,Human_Splice_Rec_227111,Human_Splice_Rec_227119 88873 RMVar_ID_88873 Human_SNP_ID_64703136 m1A Human chr2 + 27104326 27104326 27104326 CTCCATCCTTTGGGGCAGCCTGACCCGTGGGGAGCAGCAGCAGGATTAACACTGTCATCGTCAAA CTCCATCCTTTGGGGCAGCCTGACCCGTGGGGTGCAGCAGCAGGATTAACACTGTCATCGTCAAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27102581..27104427;chr2:27102581..27104434 26863196 MeRIP-seq:(Medium) rs144782472 Functional Loss SNV dbSNP153 33..33 33 - - - 88874 RMVar_ID_88874 Human_SNP_ID_64707192 m1A Human chr2 - 27118921 27118921 27118921 CGTGGAGCGGCCCGGGGGAGGCTGGCGGCGGGAGGCGAGGCGCGGGCGGCGCAGCAGCCAGGAGC CGTGGAGCGGCCCGGGGGAGGCTGGCGGCGGGCGGCGAGGCGCGGGCGGCGCAGCAGCCAGGAGC T G CGREF1 Ensembl:ENSG00000138028 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27110623..27119100;chr2:27110625..27119125 26863196 MeRIP-seq:(Medium) rs1246129599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4605102,Human_RBP_ID_18422149 Human_Splice_Rec_227049,Human_Splice_Rec_227059,Human_Splice_Rec_227073,Human_Splice_Rec_227093,Human_Splice_Rec_227103 88875 RMVar_ID_88875 Human_SNP_ID_64711552 m1A Human chr2 - 27133229 27133229 27133229 CGAGGGGCTAGAACTCAGGGTAGAGAATTTGCAGGCGGTGCAGACAGACTTTAGCTCCGATCCAC CGAGGGGCTAGAACTCAGGGTAGAGAATTTGCGGGCGGTGCAGACAGACTTTAGCTCCGATCCAC T C PREB Ensembl:ENSG00000138073 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27133178..27133279 26863196 MeRIP-seq:(Medium) rs1278037948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13840805,Human_RBP_ID_23865219 RMVar_hsa_circ_40157,RMVar_hsa_circ_107489,RMVar_hsa_circ_108509,RMVar_hsa_circ_197888,RMVar_hsa_circ_106284,RMVar_hsa_circ_76062,RMVar_hsa_circ_197889,RMVar_hsa_circ_197886,RMVar_hsa_circ_197887,RMVar_hsa_circ_116946,RMVar_hsa_circ_197891 88876 RMVar_ID_88876 Human_SNP_ID_64712015 m1A Human chr2 - 27134519 27134519 27134519 TGTGAGAGGGGTAGGGAGTGCTCCCGGCGGCGACGGGGCCGAGTTCACCAGCCGCCGGGGCAGTA TGTGAGAGGGGTAGGGAGTGCTCCCGGCGGCGGCGGGGCCGAGTTCACCAGCCGCCGGGGCAGTA T C PREB Ensembl:ENSG00000138073 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27134471..27134613 26863196 MeRIP-seq:(Medium) rs1030552879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242841,Human_RBP_ID_775839,Human_RBP_ID_830042,Human_RBP_ID_923073,Human_RBP_ID_4622303,Human_RBP_ID_5118255,Human_RBP_ID_5146520,Human_RBP_ID_5379184,Human_RBP_ID_9330963,Human_RBP_ID_22451178 RMVar_hsa_circ_107489,RMVar_hsa_circ_197886 88877 RMVar_ID_88877 Human_SNP_ID_64712020 m1A Human chr2 - 27134539 27134539 27134539 GGGTTTTGGCAACTCCCCGGTGTGAGAGGGGTAGGGAGTGCTCCCGGCGGCGACGGGGCCGAGTT GGGTTTTGGCAACTCCCCGGTGTGAGAGGGGTTGGGAGTGCTCCCGGCGGCGACGGGGCCGAGTT T A PREB Ensembl:ENSG00000138073 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27134488..27134602 26863196 MeRIP-seq:(Medium) rs951016699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775839,Human_RBP_ID_923073,Human_RBP_ID_4605180,Human_RBP_ID_5118255,Human_RBP_ID_5146520,Human_RBP_ID_5379184,Human_RBP_ID_9330963,Human_RBP_ID_22451178,Human_RBP_ID_23865220 RMVar_hsa_circ_107489,RMVar_hsa_circ_197886 88878 RMVar_ID_88878 Human_SNP_ID_64731845 m1A Human chr2 + 27212197 27212197 27212197 AGGGGGTCGGCCAGTATCCCCGAAAGAGGGCTAGGGCGCATGAAGACCAGCGCAGAGCTCCACGA AGGGGGTCGGCCAGTATCCCCGAAAGAGGGCTGGGGCGCATGAAGACCAGCGCAGAGCTCCACGA A G ATRAID Ensembl:ENSG00000138085 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27212026..27212468 26863196 MeRIP-seq:(Medium) rs1010606517 Functional Loss SNV dbSNP153 33..33 33 - - - 88879 RMVar_ID_88879 Human_SNP_ID_64731871 m1A Human chr2 + 27212232 27212232 27212232 GCGCATGAAGACCAGCGCAGAGCTCCACGAGCAGGAAAAGCCCCCAAGCAGCCCCAGGGCGACTG GCGCATGAAGACCAGCGCAGAGCTCCACGAGCCGGAAAAGCCCCCAAGCAGCCCCAGGGCGACTG A C ATRAID Ensembl:ENSG00000138085 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27212061..27212301 26863196 MeRIP-seq:(Medium) rs753882664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777030 88880 RMVar_ID_88880 Human_SNP_ID_64731872 m1A Human chr2 + 27212232 27212232 27212232 GCGCATGAAGACCAGCGCAGAGCTCCACGAGCAGGAAAAGCCCCCAAGCAGCCCCAGGGCGACTG GCGCATGAAGACCAGCGCAGAGCTCCACGAGCGGGAAAAGCCCCCAAGCAGCCCCAGGGCGACTG A G ATRAID Ensembl:ENSG00000138085 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27212061..27212301 26863196 MeRIP-seq:(Medium) rs753882664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777030 88881 RMVar_ID_88881 Human_SNP_ID_64732926 m1A Human chr2 - 27215392 27215392 27215392 GCCTTTTGGGTGGGAGGTACCTAACTACTTACATGATGACAGTGGTATGTGCCTGATGAAAGTTT GCCTTTTGGGTGGGAGGTACCTAACTACTTACGTGATGACAGTGGTATGTGCCTGATGAAAGTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27215382..27215485 26863196 MeRIP-seq:(Medium) rs1272901549 Functional Loss SNV dbSNP153 33..33 33 - - - 88882 RMVar_ID_88882 Human_SNP_ID_64733676 m1A Human chr2 - 27217516 27217516 27217516 AAGGGAGCTCAGAGGCGGGGGCGAGTACGGAGAAGCGGGAAGGACTGCAAACTCCACTGGAACCA AAGGGAGCTCAGAGGCGGGGGCGAGTACGGAGCAGCGGGAAGGACTGCAAACTCCACTGGAACCA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27217376..27217666 26863196 MeRIP-seq:(Medium) rs879510184 Functional Loss SNV dbSNP153 33..33 33 - - - 88883 RMVar_ID_88883 Human_SNP_ID_64738601 m1A Human chr2 - 27232526 27232526 27232526 AGGTATAGGTAATTTGTCTGGGCTGGCCACTCAGCTGCAACTGTGTCAATCTGTTTCACTGCTGG AGGTATAGGTAATTTGTCTGGGCTGGCCACTCCGCTGCAACTGTGTCAATCTGTTTCACTGCTGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27232476..27232575 32194978 MeRIP-seq:(Medium) rs753752679 Functional Loss SNV dbSNP153 33..33 33 - - - 88884 RMVar_ID_88884 Human_SNP_ID_64739125 m1A Human chr2 + 27234124 27234124 27234124 TCAGGTGATGCGACGCTGGTGACCCCCCCACAAGATATCACTGCCAAAACCCTGGAGCGGATCAA TCAGGTGATGCGACGCTGGTGACCCCCCCACAGGATATCACTGCCAAAACCCTGGAGCGGATCAA A G CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27234073..27234226 26863196 MeRIP-seq:(Medium) rs749662740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1300531,Human_RBP_ID_1914839 Human_miRNA_ID_2456292,Human_miRNA_ID_2461203,Human_miRNA_ID_2633860,Human_miRNA_ID_2636547 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_108530,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_371456,RMVar_hsa_circ_197930,RMVar_hsa_circ_197931,RMVar_hsa_circ_197929,RMVar_hsa_circ_7687,RMVar_hsa_circ_197937,RMVar_hsa_circ_83115,RMVar_hsa_circ_87533,RMVar_hsa_circ_77235,RMVar_hsa_circ_197938,RMVar_hsa_circ_197935,RMVar_hsa_circ_197936,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_97567,RMVar_hsa_circ_197945,RMVar_hsa_circ_76373,RMVar_hsa_circ_197946,RMVar_hsa_circ_197944,RMVar_hsa_circ_86946,RMVar_hsa_circ_119746,RMVar_hsa_circ_101201,RMVar_hsa_circ_30423,RMVar_hsa_circ_197948,RMVar_hsa_circ_197950,RMVar_hsa_circ_197952,RMVar_hsa_circ_99512,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_197954 88885 RMVar_ID_88885 Human_SNP_ID_64739252 m1A Human chr2 + 27234626 27234626 27234626 TGGACCTAGTAGCCTTGGCCACGCGGGTCATCATGGGGGAAGAAGTGGAACCTGTGGGGCTAATG TGGACCTAGTAGCCTTGGCCACGCGGGTCATCCTGGGGGAAGAAGTGGAACCTGTGGGGCTAATG A C CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27234580..27234699 26863196 MeRIP-seq:(Medium) rs767776598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56853,Human_RBP_ID_8847482,Human_RBP_ID_22991465,Human_RBP_ID_26819605 Human_Splice_Rec_227591,Human_Splice_Rec_227675,Human_Splice_Rec_227731 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_197930,RMVar_hsa_circ_197929,RMVar_hsa_circ_7687,RMVar_hsa_circ_197937,RMVar_hsa_circ_83115,RMVar_hsa_circ_87533,RMVar_hsa_circ_77235,RMVar_hsa_circ_197938,RMVar_hsa_circ_197936,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_97567,RMVar_hsa_circ_197945,RMVar_hsa_circ_76373,RMVar_hsa_circ_197946,RMVar_hsa_circ_197944,RMVar_hsa_circ_86946,RMVar_hsa_circ_119746,RMVar_hsa_circ_101201,RMVar_hsa_circ_30423,RMVar_hsa_circ_197948,RMVar_hsa_circ_197950,RMVar_hsa_circ_197952,RMVar_hsa_circ_99512,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_197954,RMVar_hsa_circ_268035 88886 RMVar_ID_88886 Human_SNP_ID_64739253 m1A Human chr2 + 27234626 27234626 27234626 TGGACCTAGTAGCCTTGGCCACGCGGGTCATCATGGGGGAAGAAGTGGAACCTGTGGGGCTAATG TGGACCTAGTAGCCTTGGCCACGCGGGTCATCGTGGGGGAAGAAGTGGAACCTGTGGGGCTAATG A G CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27234580..27234699 26863196 MeRIP-seq:(Medium) rs767776598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56853,Human_RBP_ID_8847482,Human_RBP_ID_22991465,Human_RBP_ID_26819605 Human_Splice_Rec_227591,Human_Splice_Rec_227675,Human_Splice_Rec_227731 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_197930,RMVar_hsa_circ_197929,RMVar_hsa_circ_7687,RMVar_hsa_circ_197937,RMVar_hsa_circ_83115,RMVar_hsa_circ_87533,RMVar_hsa_circ_77235,RMVar_hsa_circ_197938,RMVar_hsa_circ_197936,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_97567,RMVar_hsa_circ_197945,RMVar_hsa_circ_76373,RMVar_hsa_circ_197946,RMVar_hsa_circ_197944,RMVar_hsa_circ_86946,RMVar_hsa_circ_119746,RMVar_hsa_circ_101201,RMVar_hsa_circ_30423,RMVar_hsa_circ_197948,RMVar_hsa_circ_197950,RMVar_hsa_circ_197952,RMVar_hsa_circ_99512,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_197954,RMVar_hsa_circ_268035 88887 RMVar_ID_88887 Human_SNP_ID_64739457 m1A Human chr2 + 27235305 27235305 27235305 CGGGTGCTGACGTGGTGTTGGGTGTGGAAATGACCAGTACTGGGGAGGTGGCCGGCTTTGGGGAG CGGGTGCTGACGTGGTGTTGGGTGTGGAAATGGCCAGTACTGGGGAGGTGGCCGGCTTTGGGGAG A G CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27235229..27235372 26863196 MeRIP-seq:(Medium) rs745643074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56854,Human_RBP_ID_774873,Human_RBP_ID_3957687,Human_RBP_ID_5471206,Human_RBP_ID_9297078,Human_RBP_ID_18999120 Human_Splice_Rec_227592,Human_Splice_Rec_227676,Human_Splice_Rec_227732 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_197930,RMVar_hsa_circ_197929,RMVar_hsa_circ_7687,RMVar_hsa_circ_197937,RMVar_hsa_circ_83115,RMVar_hsa_circ_87533,RMVar_hsa_circ_197938,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_197945,RMVar_hsa_circ_76373,RMVar_hsa_circ_197946,RMVar_hsa_circ_86946,RMVar_hsa_circ_119746,RMVar_hsa_circ_101201,RMVar_hsa_circ_30423,RMVar_hsa_circ_197948,RMVar_hsa_circ_197950,RMVar_hsa_circ_197952,RMVar_hsa_circ_99512,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_119126,RMVar_hsa_circ_197954,RMVar_hsa_circ_268035,RMVar_hsa_circ_197955 88888 RMVar_ID_88888 Human_SNP_ID_64741976 m1A Human chr2 - 27242889 27242889 27242889 TAGAGCACATCAGTGTCAGGCAGCGCCTCCTCAATGCTCTCGAATTCCTCCTGGAGGGTGAGGAG TAGAGCACATCAGTGTCAGGCAGCGCCTCCTCGATGCTCTCGAATTCCTCCTGGAGGGTGAGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27242876..27242900 32194978 MeRIP-seq:(Medium) rs756487218 Functional Loss SNV dbSNP153 33..33 33 - - - 88889 RMVar_ID_88889 Human_SNP_ID_64759323 m1A Human chr2 + 27307711 27307710 27307711 GTCCCAATCGGCCGGGCCCCGCGCGGCGCGGGAAGCGCTCCGCCAGCAGCAAGAGGAGCGCGCGG GTCCCAATCGGCCGGGCCCCGCGCGGCGCGGG_AGCGCTCCGCCAGCAGCAAGAGGAGCGCGCGG GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27307664..27307773 26863196 MeRIP-seq:(Medium) rs1377021950 Functional Loss DEL dbSNP153 33..33 33 - - - 88890 RMVar_ID_88890 Human_SNP_ID_64759939 m1A Human chr2 - 27309617 27309617 27309617 CACCCATATCCCAGCAAATGCCACTCATCCCCACTCTTCATAGACACATTTGTTACTCTAACCCT CACCCATATCCCAGCAAATGCCACTCATCCCCCCTCTTCATAGACACATTTGTTACTCTAACCCT T G MPV17 Ensembl:ENSG00000115204 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27309570..27309665 26863196 MeRIP-seq:(Medium) rs1049795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548682,Human_RBP_ID_17279616,Human_RBP_ID_17390947,Human_RBP_ID_17507049,Human_RBP_ID_17954849 Human_miRNA_ID_843223,Human_miRNA_ID_1419855,Human_miRNA_ID_2724779 88891 RMVar_ID_88891 Human_SNP_ID_64761021 m1A Human chr2 - 27313073 27313073 27313073 CCTGATGGGCCTGGGTGACATTATCTCACAGCAGCTGGTGGAGAGGCGGGGTCTGCAGGAACACC CCTGATGGGCCTGGGTGACATTATCTCACAGCCGCTGGTGGAGAGGCGGGGTCTGCAGGAACACC T G MPV17 Ensembl:ENSG00000115204 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27312979..27313160 26863196 MeRIP-seq:(Medium) rs762327729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921823,Human_RBP_ID_4623190 Human_Splice_Rec_227962,Human_Splice_Rec_227963,Human_Splice_Rec_227976,Human_Splice_Rec_227977,Human_Splice_Rec_227988,Human_Splice_Rec_227989,Human_Splice_Rec_228012,Human_Splice_Rec_228013,Human_Splice_Rec_228022,Human_Splice_Rec_228023,Human_Splice_Rec_228036,Human_Splice_Rec_228037,Human_Splice_Rec_228050,Human_Splice_Rec_228051,Human_Splice_Rec_228057,Human_Splice_Rec_228068,Human_Splice_Rec_228069,Human_Splice_Rec_228094,Human_Splice_Rec_228095,Human_Splice_Rec_228108,Human_Splice_Rec_228109,Human_Splice_Rec_228120,Human_Splice_Rec_228121,Human_Splice_Rec_228136,Human_Splice_Rec_228137,Human_Splice_Rec_228146,Human_Splice_Rec_228147,Human_Splice_Rec_228151 GWAS_ID_11562 RMVar_hsa_circ_13652,RMVar_hsa_circ_368036 88892 RMVar_ID_88892 Human_SNP_ID_64763187 m1A Human chr2 + 27322428 27322428 27322428 GCTTCCAAATCAGTCTGCCCTGGTCCCACTCAAGTCCTAGAGGGACACTCACCAGCTGTCAGGAC GCTTCCAAATCAGTCTGCCCTGGTCCCACTCAGGTCCTAGAGGGACACTCACCAGCTGTCAGGAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:27322426..27322525 26863410 MeRIP-seq:(Medium) rs1276090341 Functional Loss SNV dbSNP153 33..33 33 - - - 88893 RMVar_ID_88893 Human_SNP_ID_64763222 m1A Human chr2 - 27322498 27322498 27322498 CTTGACAGGAAGCATGGCACTCTGGCGGGCATACCAGCGGGCCCTGGCCGCTCACCCGTGGAAAG CTTGACAGGAAGCATGGCACTCTGGCGGGCATGCCAGCGGGCCCTGGCCGCTCACCCGTGGAAAG T C MPV17 Ensembl:ENSG00000115204 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27322426..27322525 26863196 MeRIP-seq:(Medium) rs367838807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243450,Human_RBP_ID_917714,Human_RBP_ID_4622314,Human_RBP_ID_13841851 Human_Splice_Rec_227961,Human_Splice_Rec_227974,Human_Splice_Rec_227975,Human_Splice_Rec_227986,Human_Splice_Rec_227987,Human_Splice_Rec_228010,Human_Splice_Rec_228011,Human_Splice_Rec_228020,Human_Splice_Rec_228021,Human_Splice_Rec_228034,Human_Splice_Rec_228035,Human_Splice_Rec_228048,Human_Splice_Rec_228049,Human_Splice_Rec_228066,Human_Splice_Rec_228067,Human_Splice_Rec_228078,Human_Splice_Rec_228079,Human_Splice_Rec_228092,Human_Splice_Rec_228093,Human_Splice_Rec_228106,Human_Splice_Rec_228107,Human_Splice_Rec_228114,Human_Splice_Rec_228115,Human_Splice_Rec_228134,Human_Splice_Rec_228135,Human_Splice_Rec_228142,Human_Splice_Rec_228143,Human_Splice_Rec_228156,Human_Splice_Rec_228157,Human_Splice_Rec_228162,Human_Splice_Rec_228163,Human_Splice_Rec_228166 88894 RMVar_ID_88894 Human_SNP_ID_64769140 m1A Human chr2 + 27342934 27342934 27342934 ATTCTGGCCGATCTAGGTCTTTTGACAACTTCAGCAGCAGCAGCTCTGCCTTGGACTTTCGACCT ATTCTGGCCGATCTAGGTCTTTTGACAACTTCCGCAGCAGCAGCTCTGCCTTGGACTTTCGACCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27342885..27342975 26863196 MeRIP-seq:(Medium) rs777607074 Functional Loss SNV dbSNP153 33..33 33 - - - 88895 RMVar_ID_88895 Human_SNP_ID_64769350 m1A Human chr2 - 27343486 27343486 27343486 GAGGCCGGCCCCGTGGGGAACATGACTGTGGTAGACTCTCCTGGACAAGAGGTGCTAAATCAGCT GAGGCCGGCCCCGTGGGGAACATGACTGTGGTTGACTCTCCTGGACAAGAGGTGCTAAATCAGCT T A GTF3C2 Ensembl:ENSG00000115207 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27343436..27343600 26863196 MeRIP-seq:(Medium) rs770988753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57072,Human_RBP_ID_1585581,Human_RBP_ID_1914889,Human_RBP_ID_4623194,Human_RBP_ID_5089018,Human_RBP_ID_8516673,Human_RBP_ID_8847564,Human_RBP_ID_9330395,Human_RBP_ID_13842108,Human_RBP_ID_17954882,Human_RBP_ID_18758436,Human_RBP_ID_22076176,Human_RBP_ID_22451192,Human_RBP_ID_22743182,Human_RBP_ID_23119403,Human_RBP_ID_27010374,Human_RBP_ID_27563803 Human_Splice_Rec_228168,Human_Splice_Rec_228204,Human_Splice_Rec_228318,Human_Splice_Rec_228324 Human_miRNA_ID_2054661,Human_miRNA_ID_2991818 RMVar_hsa_circ_4065,RMVar_hsa_circ_110068,RMVar_hsa_circ_197975,RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_21353,RMVar_hsa_circ_25458,RMVar_hsa_circ_197985,RMVar_hsa_circ_15678,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_339766,RMVar_hsa_circ_368158,RMVar_hsa_circ_197987 88896 RMVar_ID_88896 Human_SNP_ID_64769351 m1A Human chr2 - 27343486 27343486 27343486 GAGGCCGGCCCCGTGGGGAACATGACTGTGGTAGACTCTCCTGGACAAGAGGTGCTAAATCAGCT GAGGCCGGCCCCGTGGGGAACATGACTGTGGTCGACTCTCCTGGACAAGAGGTGCTAAATCAGCT T G GTF3C2 Ensembl:ENSG00000115207 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27343436..27343600 26863196 MeRIP-seq:(Medium) rs770988753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57072,Human_RBP_ID_1585581,Human_RBP_ID_1914889,Human_RBP_ID_4623194,Human_RBP_ID_5089018,Human_RBP_ID_8516673,Human_RBP_ID_8847564,Human_RBP_ID_9330395,Human_RBP_ID_13842108,Human_RBP_ID_17954882,Human_RBP_ID_18758436,Human_RBP_ID_22076176,Human_RBP_ID_22451192,Human_RBP_ID_22743182,Human_RBP_ID_23119403,Human_RBP_ID_27010374,Human_RBP_ID_27563803 Human_Splice_Rec_228168,Human_Splice_Rec_228204,Human_Splice_Rec_228318,Human_Splice_Rec_228324 Human_miRNA_ID_2054661,Human_miRNA_ID_2991818 RMVar_hsa_circ_4065,RMVar_hsa_circ_110068,RMVar_hsa_circ_197975,RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_21353,RMVar_hsa_circ_25458,RMVar_hsa_circ_197985,RMVar_hsa_circ_15678,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_339766,RMVar_hsa_circ_368158,RMVar_hsa_circ_197987 88897 RMVar_ID_88897 Human_SNP_ID_64769356 m1A Human chr2 - 27343500 27343500 27343500 ATGTTGCCCTGGGGGAGGCCGGCCCCGTGGGGAACATGACTGTGGTAGACTCTCCTGGACAAGAG ATGTTGCCCTGGGGGAGGCCGGCCCCGTGGGGGACATGACTGTGGTAGACTCTCCTGGACAAGAG T C GTF3C2 Ensembl:ENSG00000115207 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27343451..27343600 26863196 MeRIP-seq:(Medium) rs767299084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57072,Human_RBP_ID_4622315,Human_RBP_ID_5089018,Human_RBP_ID_8516673,Human_RBP_ID_9330395,Human_RBP_ID_17954882,Human_RBP_ID_18193270,Human_RBP_ID_22076176,Human_RBP_ID_22451192,Human_RBP_ID_22743182,Human_RBP_ID_23119403 Human_Splice_Rec_228168,Human_Splice_Rec_228204,Human_Splice_Rec_228318,Human_Splice_Rec_228324 Human_miRNA_ID_2054661 RMVar_hsa_circ_4065,RMVar_hsa_circ_110068,RMVar_hsa_circ_197975,RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_21353,RMVar_hsa_circ_25458,RMVar_hsa_circ_197985,RMVar_hsa_circ_15678,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_339766,RMVar_hsa_circ_368158,RMVar_hsa_circ_197987 88898 RMVar_ID_88898 Human_SNP_ID_64771800 m1A Human chr2 - 27352464 27352464 27352464 AGATGGGGGAATGGGGCTAGAACACAAGTGAAAGGTTTGGTGTTAGAGAGTGAATGAAGGTGTCA AGATGGGGGAATGGGGCTAGAACACAAGTGAAGGGTTTGGTGTTAGAGAGTGAATGAAGGTGTCA T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27352461..27352595 26863196 MeRIP-seq:(Medium) rs549799387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828450,Human_RBP_ID_13842301 RMVar_hsa_circ_197986,RMVar_hsa_circ_128167 88899 RMVar_ID_88899 Human_SNP_ID_64773100 m1A Human chr2 + 27356729 27356729 27356729 ATTGTGGGGCCCCCCACACACCCGCTGCGGCGATACACTCACCCTCGCCAAAGTCCTTCCGGAAG ATTGTGGGGCCCCCCACACACCCGCTGCGGCGGTACACTCACCCTCGCCAAAGTCCTTCCGGAAG A G AC074117.1 Ensembl:ENSG00000234072 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27356726..27356775 26863196 MeRIP-seq:(Medium) rs548530271 Functional Loss SNV dbSNP153 33..33 33 - - - 88900 RMVar_ID_88900 Human_SNP_ID_64773326 m1A Human chr2 + 27357327 27357327 27357327 CAGGGATGGGCCCGAGAGAGCTTGGAAAGAGGACAAGGAAGGGAAGGAGTAGGAGTAGAAAAGCA CAGGGATGGGCCCGAGAGAGCTTGGAAAGAGGGCAAGGAAGGGAAGGAGTAGGAGTAGAAAAGCA A G AC074117.1 Ensembl:ENSG00000234072 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27357095..27357387;chr2:27357120..27357407 26863196 MeRIP-seq:(Medium) rs1211338516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827898,Human_RBP_ID_4625817,Human_RBP_ID_5594439,Human_RBP_ID_6906243,Human_RBP_ID_8516688,Human_RBP_ID_9383335,Human_RBP_ID_13842445,Human_RBP_ID_22250461,Human_RBP_ID_27010386 88901 RMVar_ID_88901 Human_SNP_ID_64774095 m1A Human chr2 + 27359504 27359483 27359504 CTCTGCCCGGCCGCCCCGTCTGAGAAGTGAGGAGCCACCCCATCTGGGAAGTGAGGAGCATCTCC CTCTGCCCGGCC_____________________GCCACCCCATCTGGGAAGTGAGGAGCATCTCC CGCCCCGTCTGAGAAGTGAGGA C AC074117.1 Ensembl:ENSG00000234072 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27359468..27359542 26863196 MeRIP-seq:(Medium) rs1458248323 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_827901,Human_RBP_ID_919962,Human_RBP_ID_9386204 88902 RMVar_ID_88902 Human_SNP_ID_64774111 m1A Human chr2 + 27359504 27359504 27359504 CTCTGCCCGGCCGCCCCGTCTGAGAAGTGAGGAGCCACCCCATCTGGGAAGTGAGGAGCATCTCC CTCTGCCCGGCCGCCCCGTCTGAGAAGTGAGGCGCCACCCCATCTGGGAAGTGAGGAGCATCTCC A C AC074117.1 Ensembl:ENSG00000234072 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27359468..27359542 26863196 MeRIP-seq:(Medium) rs1317408833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827901,Human_RBP_ID_919962,Human_RBP_ID_9386204 88903 RMVar_ID_88903 Human_SNP_ID_64777963 m1A Human chr2 - 27370229 27370229 27370229 CTACTGGTACGCGGAGCCGACGAGCTCCGGACAGCTAGTGCCGGGCCTTGAGCGCCTTTGGGCCC CTACTGGTACGCGGAGCCGACGAGCTCCGGACGGCTAGTGCCGGGCCTTGAGCGCCTTTGGGCCC T C EIF2B4 Ensembl:ENSG00000115211 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27370226..27370383 26863196 MeRIP-seq:(Medium) rs1558296900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23258004 88904 RMVar_ID_88904 Human_SNP_ID_64778224 m1A Human chr2 + 27370676 27370676 27370676 GAGTGAGGCTGCGGGGACTCGCTGAGCAGCGGAGGGGGAGCGTGCAGAGCCGCTGCGGCCCTCAC GAGTGAGGCTGCGGGGACTCGCTGAGCAGCGGGGGGGGAGCGTGCAGAGCCGCTGCGGCCCTCAC A G SNX17 Ensembl:ENSG00000115234 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:27370626..27370831;chr2:27370626..27370775;chr2:27370626..27370740 26863196 MeRIP-seq:(Medium) rs903889917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242418,Human_RBP_ID_830200,Human_RBP_ID_4622317,Human_RBP_ID_22450271 Human_miRNA_ID_2394344,Human_miRNA_ID_3067921 RMVar_hsa_circ_87588,RMVar_hsa_circ_197995 88905 RMVar_ID_88905 Human_SNP_ID_64778489 m1A Human chr2 + 27371300 27371300 27371300 GGCCTATAACATTCACGTGAATGGAGTCCTGCACTGTCGGGTGCGCTACAGCCAGCTCCTGGGGC GGCCTATAACATTCACGTGAATGGAGTCCTGCGCTGTCGGGTGCGCTACAGCCAGCTCCTGGGGC A G SNX17 Ensembl:ENSG00000115234 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27370693..27371305 32194978 MeRIP-seq:(Medium) rs1558299919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548754,Human_RBP_ID_1585595,Human_RBP_ID_4622318,Human_RBP_ID_8852595 Human_Splice_Rec_228622,Human_Splice_Rec_228624,Human_Splice_Rec_228625,Human_Splice_Rec_228652,Human_Splice_Rec_228678,Human_Splice_Rec_228679,Human_Splice_Rec_228692,Human_Splice_Rec_228693,Human_Splice_Rec_228722,Human_Splice_Rec_228723,Human_Splice_Rec_228728,Human_Splice_Rec_228729 Human_miRNA_ID_794535,Human_miRNA_ID_1997454,Human_miRNA_ID_2077631,Human_miRNA_ID_2079957,Human_miRNA_ID_2090497 RMVar_hsa_circ_64864,RMVar_hsa_circ_120420,RMVar_hsa_circ_87588,RMVar_hsa_circ_197995,RMVar_hsa_circ_97893,RMVar_hsa_circ_197996,RMVar_hsa_circ_197997 88906 RMVar_ID_88906 Human_SNP_ID_64780449 m1A Human chr2 + 27376725 27376725 27376725 GAGGGCATTGGAGATGAGGATCTGTAATCTCCACTGCTTGGATGTCTGCCCTCTACCCCAGAGGA GAGGGCATTGGAGATGAGGATCTGTAATCTCCGCTGCTTGGATGTCTGCCCTCTACCCCAGAGGA A G SNX17 Ensembl:ENSG00000115234 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27376601..27376939 32194978 MeRIP-seq:(Medium) rs750907206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1914944,Human_RBP_ID_3621923,Human_RBP_ID_13842704,Human_RBP_ID_17658417,Human_RBP_ID_27479436 Human_miRNA_ID_1983865,Human_miRNA_ID_2939504 RMVar_hsa_circ_87588,RMVar_hsa_circ_197995,RMVar_hsa_circ_97893,RMVar_hsa_circ_117732,RMVar_hsa_circ_197997,RMVar_hsa_circ_114816,RMVar_hsa_circ_197998,RMVar_hsa_circ_79525,RMVar_hsa_circ_197999,RMVar_hsa_circ_119307,RMVar_hsa_circ_198000,RMVar_hsa_circ_90954,RMVar_hsa_circ_198002,RMVar_hsa_circ_198003,RMVar_hsa_circ_112944,RMVar_hsa_circ_198004 88907 RMVar_ID_88907 Human_SNP_ID_64780575 m1A Human chr2 + 27377100 27377100 27377100 AGAGGTCTGTGTTTGGTCTGGCCCAGTTCCCCATCATTAAACTCAGCCTGACTGCTGCCTACCTC AGAGGTCTGTGTTTGGTCTGGCCCAGTTCCCCGTCATTAAACTCAGCCTGACTGCTGCCTACCTC A G SNX17 Ensembl:ENSG00000115234 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27377051..27377100 32194978 MeRIP-seq:(Medium) rs1316255284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548777,Human_RBP_ID_3621925,Human_RBP_ID_18316179,Human_RBP_ID_18758461 RMVar_hsa_circ_87588,RMVar_hsa_circ_197995,RMVar_hsa_circ_97893,RMVar_hsa_circ_117732,RMVar_hsa_circ_197997,RMVar_hsa_circ_114816,RMVar_hsa_circ_197998,RMVar_hsa_circ_79525,RMVar_hsa_circ_197999,RMVar_hsa_circ_119307,RMVar_hsa_circ_198000,RMVar_hsa_circ_90954,RMVar_hsa_circ_198002,RMVar_hsa_circ_198003,RMVar_hsa_circ_112944,RMVar_hsa_circ_198004 88908 RMVar_ID_88908 Human_SNP_ID_64780954 m1A Human chr2 + 27378019 27378019 27378019 TAAGGACAGCGGGCGCAGCGGAAGGGCTTCTCACCACTGTGTGTCTTCATGTGCCGGGCCAGGTG TAAGGACAGCGGGCGCAGCGGAAGGGCTTCTCGCCACTGTGTGTCTTCATGTGCCGGGCCAGGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27377978..27378243 26863196 MeRIP-seq:(Medium) rs145897230 Functional Loss SNV dbSNP153 33..33 33 - - - 88909 RMVar_ID_88909 Human_SNP_ID_64781213 m1A Human chr2 + 27378564 27378564 27378564 GTACAGCAGCGGAAGCCACAGGTCGGGCAGGGAGGAGTGGGGGGCCCTGCGTGGGTACGCTGATG GTACAGCAGCGGAAGCCACAGGTCGGGCAGGGTGGAGTGGGGGGCCCTGCGTGGGTACGCTGATG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27378516..27378741;chr2:27378520..27378676 26863196 MeRIP-seq:(Medium) rs1475358513 Functional Loss SNV dbSNP153 33..33 33 - - - 88910 RMVar_ID_88910 Human_SNP_ID_64782031 m1A Human chr2 - 27380599 27380599 27380599 GCGGCCCGCGGGCCCTGAGAGGAAGGGCAGACAGGCGGGCCGAGATAGGAGGGGCGGGGTCGGGC GCGGCCCGCGGGCCCTGAGAGGAAGGGCAGACGGGCGGGCCGAGATAGGAGGGGCGGGGTCGGGC T C ZNF513 Ensembl:ENSG00000163795 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:27378870..27380733;chr2:27380345..27380750 26863196 MeRIP-seq:(Medium) rs1379139130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_917029,Human_RBP_ID_4624163,Human_RBP_ID_5379256,Human_RBP_ID_18421730 88911 RMVar_ID_88911 Human_SNP_ID_64782071 m1A Human chr2 + 27380690 27380690 27380690 CAGCCCCCGGCCCTGGCCCCGGCGCCCAGCTCAGGCCGCTCCCGCCGCCGCCGCCGCTTCCATTC CAGCCCCCGGCCCTGGCCCCGGCGCCCAGCTCGGGCCGCTCCCGCCGCCGCCGCCGCTTCCATTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27380432..27380750 26863196 MeRIP-seq:(Medium) rs1183471150 Functional Loss SNV dbSNP153 33..33 33 - - - 88912 RMVar_ID_88912 Human_SNP_ID_64782321 m1A Human chr2 + 27381307 27381304 27381308 CATGGAGCCGCCAATAAAAAAGAATGTCCTTAAATAAAGTTCACAGAGTAAAAACCAGAACCGCC CATGGAGCCGCCAATAAAAAAGAATGTCCT____TAAAGTTCACAGAGTAAAAACCAGAACCGCC TTAAA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27381256..27381339 26863196 MeRIP-seq:(Medium) rs1229259520 Functional Loss DEL dbSNP153 31..34 33 - - - 88913 RMVar_ID_88913 Human_SNP_ID_64782402 m1A Human chr2 - 27381605 27381605 27381605 GGCAACAGCGACAAGAAGAAGAAGGCCAAGCGAGACTAGCAGTCATCCAGACCCCTGCCCACCTA GGCAACAGCGACAAGAAGAAGAAGGCCAAGCGGGACTAGCAGTCATCCAGACCCCTGCCCACCTA T C PPM1G Ensembl:ENSG00000115241 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27381554..27381743;chr2:27381555..27381707 26863196 MeRIP-seq:(Medium) rs752092055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84630,RMVar_hsa_circ_116369,RMVar_hsa_circ_127529,RMVar_hsa_circ_118417,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_198011,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198012,RMVar_hsa_circ_198009,RMVar_hsa_circ_198010,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006 88914 RMVar_ID_88914 Human_SNP_ID_64782420 m1A Human chr2 + 27381647 27381647 27381647 TTCTTCTTCTTGTCGCTGTTGCCATTTTCTTCAGCCCCCTCAGTAGAGAGCACCTCCTCTAGTTT TTCTTCTTCTTGTCGCTGTTGCCATTTTCTTCGGCCCCCTCAGTAGAGAGCACCTCCTCTAGTTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27381597..27381687 26863196 MeRIP-seq:(Medium) rs1294423218 Functional Loss SNV dbSNP153 33..33 33 - - - 88915 RMVar_ID_88915 Human_SNP_ID_64783052 m1A Human chr2 - 27384043 27384043 27384043 GGATGGCTACAGCAGTGAGGAGGCAGAGAATGAGGAAGATGAGGATGACACCGAGGAGGCTGAAG GGATGGCTACAGCAGTGAGGAGGCAGAGAATGGGGAAGATGAGGATGACACCGAGGAGGCTGAAG T C PPM1G Ensembl:ENSG00000115241 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27383902..27384139 26863196 MeRIP-seq:(Medium) rs147058083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57107,Human_RBP_ID_206136,Human_RBP_ID_830905,Human_RBP_ID_1592319,Human_RBP_ID_1914964,Human_RBP_ID_2634942,Human_RBP_ID_3957709,Human_RBP_ID_6906329,Human_RBP_ID_9383371,Human_RBP_ID_13842806,Human_RBP_ID_18412607,Human_RBP_ID_18533560,Human_RBP_ID_20618534,Human_RBP_ID_22077997,Human_RBP_ID_22417065,Human_RBP_ID_22996797,Human_RBP_ID_23119273,Human_RBP_ID_23865510,Human_RBP_ID_24545769,Human_RBP_ID_26338498,Human_RBP_ID_27816906 Human_Splice_Rec_228780,Human_Splice_Rec_228781,Human_Splice_Rec_228798,Human_Splice_Rec_228799 RMVar_hsa_circ_77378,RMVar_hsa_circ_127529,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198009,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006,RMVar_hsa_circ_198016,RMVar_hsa_circ_127075,RMVar_hsa_circ_311062,RMVar_hsa_circ_198017,RMVar_hsa_circ_198018,RMVar_hsa_circ_53824 88916 RMVar_ID_88916 Human_SNP_ID_64783060 m1A Human chr2 + 27384072 27384072 27384072 TCCTCATTCTCTGCCTCCTCACTGCTGTAGCCATCCTCTTCCTCGCTGCATTCCTGCCAGGGGGA TCCTCATTCTCTGCCTCCTCACTGCTGTAGCCGTCCTCTTCCTCGCTGCATTCCTGCCAGGGGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:27383893..27384135;chr2:27383920..27384134 26863196 MeRIP-seq:(Medium) rs1482855351 Functional Loss SNV dbSNP153 33..33 33 - - - 88917 RMVar_ID_88917 Human_SNP_ID_64783182 m1A Human chr2 - 27384635 27384635 27384635 GGCCTGTGAGGGCAGGCAGATGCTGAAGTTGCAGAGAGGTCCTGTTTGGTTGCCGTCTGTAGTTT GGCCTGTGAGGGCAGGCAGATGCTGAAGTTGCGGAGAGGTCCTGTTTGGTTGCCGTCTGTAGTTT T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27384633..27385130 26863196 MeRIP-seq:(Medium) rs371626492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77378,RMVar_hsa_circ_127529,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198009,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006,RMVar_hsa_circ_198016,RMVar_hsa_circ_127075,RMVar_hsa_circ_311062,RMVar_hsa_circ_198017,RMVar_hsa_circ_198018,RMVar_hsa_circ_53824 88918 RMVar_ID_88918 Human_SNP_ID_64783200 m1A Human chr2 - 27384720 27384720 27384720 CTCGAGTTGCTAAGTCCAAGTTCTTTGAGGACAGTGAGGATGAGTCAGATGAGGCGGAGGAAGAA CTCGAGTTGCTAAGTCCAAGTTCTTTGAGGACGGTGAGGATGAGTCAGATGAGGCGGAGGAAGAA T C PPM1G Ensembl:ENSG00000115241 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1185691280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57108,Human_RBP_ID_264353,Human_RBP_ID_548814,Human_RBP_ID_1914967,Human_RBP_ID_3621938,Human_RBP_ID_6906335,Human_RBP_ID_8516727,Human_RBP_ID_8847587,Human_RBP_ID_9105192,Human_RBP_ID_13842825,Human_RBP_ID_18758483,Human_RBP_ID_22074675,Human_RBP_ID_23865511,Human_RBP_ID_26338499 Human_Splice_Rec_228778,Human_Splice_Rec_228779,Human_Splice_Rec_228797 Human_miRNA_ID_2453279 RMVar_hsa_circ_77378,RMVar_hsa_circ_127529,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198009,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006,RMVar_hsa_circ_198016,RMVar_hsa_circ_127075,RMVar_hsa_circ_311062,RMVar_hsa_circ_198017,RMVar_hsa_circ_198018,RMVar_hsa_circ_343425,RMVar_hsa_circ_53824 88919 RMVar_ID_88919 Human_SNP_ID_64783294 m1A Human chr2 - 27385001 27384996 27385002 GCTGCTGACACGCTACGGGCAGAACTGTCACAAGGGCCCTCCCCACAGCAAATCTGGAGGTGGGA GCTGCTGACACGCTACGGGCAGAACTGTCAC______CCTCCCCACAGCAAATCTGGAGGTGGGA GGCCCTT G PPM1G Ensembl:ENSG00000115241 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27384951..27385000 32194978 MeRIP-seq:(Medium) rs1240632424 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_57109,Human_RBP_ID_8234267,Human_RBP_ID_8851111,Human_RBP_ID_9105194,Human_RBP_ID_9330969,Human_RBP_ID_9383376,Human_RBP_ID_18193468,Human_RBP_ID_26338502,Human_RBP_ID_27010472,Human_RBP_ID_27816908 Human_Splice_Rec_228777,Human_Splice_Rec_228796 Human_miRNA_ID_2365936,Human_miRNA_ID_2724781,Human_miRNA_ID_3013739,Human_miRNA_ID_3066694 RMVar_hsa_circ_77378,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006,RMVar_hsa_circ_198016,RMVar_hsa_circ_127075,RMVar_hsa_circ_311062,RMVar_hsa_circ_198017,RMVar_hsa_circ_198018,RMVar_hsa_circ_343425,RMVar_hsa_circ_53824 88920 RMVar_ID_88920 Human_SNP_ID_64783298 m1A Human chr2 - 27385004 27385004 27385004 AGAGCTGCTGACACGCTACGGGCAGAACTGTCACAAGGGCCCTCCCCACAGCAAATCTGGAGGTG AGAGCTGCTGACACGCTACGGGCAGAACTGTCGCAAGGGCCCTCCCCACAGCAAATCTGGAGGTG T C PPM1G Ensembl:ENSG00000115241 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27384814..27385245 26863196 MeRIP-seq:(Medium) rs758422602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57109,Human_RBP_ID_775064,Human_RBP_ID_8234267,Human_RBP_ID_8847593,Human_RBP_ID_9330969,Human_RBP_ID_9383376,Human_RBP_ID_18193468,Human_RBP_ID_26338502,Human_RBP_ID_27010472,Human_RBP_ID_27816908 Human_Splice_Rec_228777,Human_Splice_Rec_228796 Human_miRNA_ID_2365936,Human_miRNA_ID_2724781,Human_miRNA_ID_2876409,Human_miRNA_ID_3013739,Human_miRNA_ID_3066694 RMVar_hsa_circ_77378,RMVar_hsa_circ_98725,RMVar_hsa_circ_198007,RMVar_hsa_circ_79371,RMVar_hsa_circ_80687,RMVar_hsa_circ_78831,RMVar_hsa_circ_198008,RMVar_hsa_circ_198005,RMVar_hsa_circ_198006,RMVar_hsa_circ_198016,RMVar_hsa_circ_127075,RMVar_hsa_circ_311062,RMVar_hsa_circ_198017,RMVar_hsa_circ_198018,RMVar_hsa_circ_343425,RMVar_hsa_circ_53824 88921 RMVar_ID_88921 Human_SNP_ID_64789912 m1A Human chr2 + 27409417 27409417 27409417 CACTTCACCGTGTTGGGCTGGGAGAGGTAGGCACCCATGGCGGCGGCTGGCCGGCGGCCTCAGGT CACTTCACCGTGTTGGGCTGGGAGAGGTAGGCGCCCATGGCGGCGGCTGGCCGGCGGCCTCAGGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:27409376..27409475 26863196 MeRIP-seq:(Medium) rs1390639781 Functional Loss SNV dbSNP153 33..33 33 - - - 88922 RMVar_ID_88922 Human_SNP_ID_64789943 m1A Human chr2 + 27409479 27409479 27409479 GGTGCAGGAAAGCTGGGCGCGACCCGTGCCGGAGCCGAAGCCCCGGGGGTGCGCGCGGCAGGAGC GGTGCAGGAAAGCTGGGCGCGACCCGTGCCGGTGCCGAAGCCCCGGGGGTGCGCGCGGCAGGAGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27409430..27409600 26863196 MeRIP-seq:(Medium) rs185804071 Functional Loss SNV dbSNP153 33..33 33 - - - 88923 RMVar_ID_88923 Human_SNP_ID_64789944 m1A Human chr2 + 27409484 27409484 27409484 AGGAAAGCTGGGCGCGACCCGTGCCGGAGCCGAAGCCCCGGGGGTGCGCGCGGCAGGAGCAGGCC AGGAAAGCTGGGCGCGACCCGTGCCGGAGCCGCAGCCCCGGGGGTGCGCGCGGCAGGAGCAGGCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:27409351..27409600 26863410 MeRIP-seq:(Medium) rs1427495193 Functional Loss SNV dbSNP153 33..33 33 - - - 88924 RMVar_ID_88924 Human_SNP_ID_64798393 m1A Human chr2 + 27440877 27440877 27440877 CCCCAGCAGCCACAGCAGGAGGAGGTGACATCACCTGTCGTGCCCCCCTCTGTCAAGACTCCGAC CCCCAGCAGCCACAGCAGGAGGAGGTGACATCTCCTGTCGTGCCCCCCTCTGTCAAGACTCCGAC A T NRBP1 Ensembl:ENSG00000115216 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27440826..27441127 32194978 MeRIP-seq:(Medium) rs1045332329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22451202 Human_Splice_Rec_228836,Human_Splice_Rec_228837,Human_Splice_Rec_228870,Human_Splice_Rec_228871,Human_Splice_Rec_228906,Human_Splice_Rec_228907,Human_Splice_Rec_228948,Human_Splice_Rec_228949,Human_Splice_Rec_228958,Human_Splice_Rec_228959 Human_miRNA_ID_2889339 RMVar_hsa_circ_7263,RMVar_hsa_circ_198033,RMVar_hsa_circ_101480,RMVar_hsa_circ_21406,RMVar_hsa_circ_370551,RMVar_hsa_circ_12472,RMVar_hsa_circ_198034 88925 RMVar_ID_88925 Human_SNP_ID_64798731 m1A Human chr2 - 27441838 27441838 27441838 GGCTGCAGCACGTCCAGGGACAGCCACAGCGCAGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG GGCTGCAGCACGTCCAGGGACAGCCACAGCGCGGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27441710..27442209 32194978 MeRIP-seq:(Medium) rs753974931 Functional Loss SNV dbSNP153 33..33 33 - - - 88926 RMVar_ID_88926 Human_SNP_ID_64798732 m1A Human chr2 - 27441838 27441838 27441838 GGCTGCAGCACGTCCAGGGACAGCCACAGCGCAGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG GGCTGCAGCACGTCCAGGGACAGCCACAGCGCCGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27441710..27442209 32194978 MeRIP-seq:(Medium) rs753974931 Functional Loss SNV dbSNP153 33..33 33 - - - 88927 RMVar_ID_88927 Human_SNP_ID_64798746 m1A Human chr2 + 27441867 27441867 27441867 ATCTGCGCTGTGGCTGTCCCTGGACGTGCTGCAGCCCTCCTGTCCCTTCCCCCCAGTCAGTATTA ATCTGCGCTGTGGCTGTCCCTGGACGTGCTGCGGCCCTCCTGTCCCTTCCCCCCAGTCAGTATTA A G NRBP1 Ensembl:ENSG00000115216 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27441820..27441912 26863196 MeRIP-seq:(Medium) rs955712651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548835,Human_RBP_ID_17392596,Human_RBP_ID_17509616,Human_RBP_ID_17658431,Human_RBP_ID_18949050,Human_RBP_ID_26338511,Human_RBP_ID_27479495 Human_miRNA_ID_205568,Human_miRNA_ID_1322096,Human_miRNA_ID_1478694 RMVar_hsa_circ_107240,RMVar_hsa_circ_198035 88928 RMVar_ID_88928 Human_SNP_ID_64812689 m1A Human chr2 + 27493459 27493459 27493459 TCCCCAGTCTGCAGTGGCCGCTCTCCATCCAGACCTTCCACTGTGATGTCACCTGAGAAGGGAGA TCCCCAGTCTGCAGTGGCCGCTCTCCATCCAGCCCTTCCACTGTGATGTCACCTGAGAAGGGAGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27493410..27494110 32194978 MeRIP-seq:(Medium) rs768443253 Functional Loss SNV dbSNP153 33..33 33 - - - 88929 RMVar_ID_88929 Human_SNP_ID_64812690 m1A Human chr2 + 27493459 27493459 27493459 TCCCCAGTCTGCAGTGGCCGCTCTCCATCCAGACCTTCCACTGTGATGTCACCTGAGAAGGGAGA TCCCCAGTCTGCAGTGGCCGCTCTCCATCCAGGCCTTCCACTGTGATGTCACCTGAGAAGGGAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27493410..27494110 32194978 MeRIP-seq:(Medium) rs768443253 Functional Loss SNV dbSNP153 33..33 33 - - - 88930 RMVar_ID_88930 Human_SNP_ID_64813048 m1A Human chr2 + 27494582 27494582 27494582 CTCGCACGAAGCCCAGGTCACAGCTGACCAGCAGGAGGACCGTGGGGCTTAGATATGGGGAAAGG CTCGCACGAAGCCCAGGTCACAGCTGACCAGCCGGAGGACCGTGGGGCTTAGATATGGGGAAAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27494466..27494583 32194978 MeRIP-seq:(Medium) rs1446010937 Functional Loss SNV dbSNP153 33..33 33 - - - 88931 RMVar_ID_88931 Human_SNP_ID_64835771 m1A Human chr2 - 27583626 27583626 27583626 TCTAGCAAATCACAAGCACACGAGTGAGTGCTAGGGACCTCTGAACCTCGACCACAAAAAGACGA TCTAGCAAATCACAAGCACACGAGTGAGTGCTTGGGACCTCTGAACCTCGACCACAAAAAGACGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27583621..27583690 26863196 MeRIP-seq:(Medium) rs758537382 Functional Loss SNV dbSNP153 33..33 33 - - - 88932 RMVar_ID_88932 Human_SNP_ID_64847043 m1A Human chr2 + 27629073 27629073 27629073 GGTGGGGCCAGGAGGAAGATGGCGGCGTCCGCAGCTGCCGCTGAGCTCCAGGCTTCTGGGGGTCC GGTGGGGCCAGGAGGAAGATGGCGGCGTCCGCCGCTGCCGCTGAGCTCCAGGCTTCTGGGGGTCC A C AC074091.2,GPN1 Ensembl:ENSG00000259080,Ensembl:ENSG00000198522 lincRNA,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27629026..27629192 26863196 MeRIP-seq:(Medium) rs756513042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827852,Human_RBP_ID_4606169,Human_RBP_ID_8203379 Human_Splice_Rec_229843,Human_Splice_Rec_229869,Human_Splice_Rec_229895,Human_Splice_Rec_229907,Human_Splice_Rec_229933 RMVar_hsa_circ_119954,RMVar_hsa_circ_198069 88933 RMVar_ID_88933 Human_SNP_ID_64847053 m1A Human chr2 - 27629082 27629082 27629082 GGGTGCCGCGGACCCCCAGAAGCCTGGAGCTCAGCGGCAGCTGCGGACGCCGCCATCTTCCTCCT GGGTGCCGCGGACCCCCAGAAGCCTGGAGCTCCGCGGCAGCTGCGGACGCCGCCATCTTCCTCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27629026..27629175;chr2:27629026..27629193 26863196 MeRIP-seq:(Medium) rs1463843042 Functional Loss SNV dbSNP153 33..33 33 - - - 88934 RMVar_ID_88934 Human_SNP_ID_64847054 m1A Human chr2 + 27629084 27629084 27629084 GAGGAAGATGGCGGCGTCCGCAGCTGCCGCTGAGCTCCAGGCTTCTGGGGGTCCGCGGCACCCAG GAGGAAGATGGCGGCGTCCGCAGCTGCCGCTGCGCTCCAGGCTTCTGGGGGTCCGCGGCACCCAG A C AC074091.2,GPN1 Ensembl:ENSG00000259080,Ensembl:ENSG00000198522 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27629026..27629232 26863196 MeRIP-seq:(Medium) rs1169068979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827852,Human_RBP_ID_4606170 Human_Splice_Rec_229843,Human_Splice_Rec_229869,Human_Splice_Rec_229895,Human_Splice_Rec_229907,Human_Splice_Rec_229933 Human_miRNA_ID_2468095 RMVar_hsa_circ_119954,RMVar_hsa_circ_198069 88935 RMVar_ID_88935 Human_SNP_ID_64847055 m1A Human chr2 + 27629084 27629084 27629084 GAGGAAGATGGCGGCGTCCGCAGCTGCCGCTGAGCTCCAGGCTTCTGGGGGTCCGCGGCACCCAG GAGGAAGATGGCGGCGTCCGCAGCTGCCGCTGGGCTCCAGGCTTCTGGGGGTCCGCGGCACCCAG A G AC074091.2,GPN1 Ensembl:ENSG00000259080,Ensembl:ENSG00000198522 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27629026..27629232 26863196 MeRIP-seq:(Medium) rs1169068979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827852,Human_RBP_ID_4606170 Human_Splice_Rec_229843,Human_Splice_Rec_229869,Human_Splice_Rec_229895,Human_Splice_Rec_229907,Human_Splice_Rec_229933 Human_miRNA_ID_2468095 RMVar_hsa_circ_119954,RMVar_hsa_circ_198069 88936 RMVar_ID_88936 Human_SNP_ID_64847070 m1A Human chr2 - 27629097 27629097 27629097 ACCAACAGACACACTGGGTGCCGCGGACCCCCAGAAGCCTGGAGCTCAGCGGCAGCTGCGGACGC ACCAACAGACACACTGGGTGCCGCGGACCCCCTGAAGCCTGGAGCTCAGCGGCAGCTGCGGACGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27629047..27629175 26863196 MeRIP-seq:(Medium) rs1553356303 Functional Loss SNV dbSNP153 33..33 33 - - - 88937 RMVar_ID_88937 Human_SNP_ID_64847071 m1A Human chr2 - 27629097 27629097 27629097 ACCAACAGACACACTGGGTGCCGCGGACCCCCAGAAGCCTGGAGCTCAGCGGCAGCTGCGGACGC ACCAACAGACACACTGGGTGCCGCGGACCCCCGGAAGCCTGGAGCTCAGCGGCAGCTGCGGACGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27629047..27629175 26863196 MeRIP-seq:(Medium) rs1553356303 Functional Loss SNV dbSNP153 33..33 33 - - - 88938 RMVar_ID_88938 Human_SNP_ID_64847110 m1A Human chr2 + 27629158 27629158 27629158 TGGTGTTGGGAATGGCGGGATCCGGGAAAACCACTTTTGTACAGGTGACGTACACAGCATGGGTG TGGTGTTGGGAATGGCGGGATCCGGGAAAACCGCTTTTGTACAGGTGACGTACACAGCATGGGTG A G AC074091.2,GPN1 Ensembl:ENSG00000259080,Ensembl:ENSG00000198522 lincRNA,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:27629035..27629175 26863196 MeRIP-seq:(Medium) rs924806822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624173,Human_RBP_ID_19099752,Human_RBP_ID_21893549 Human_Splice_Rec_229843,Human_Splice_Rec_229869,Human_Splice_Rec_229895,Human_Splice_Rec_229907,Human_Splice_Rec_229933 Human_miRNA_ID_2057159 RMVar_hsa_circ_119954,RMVar_hsa_circ_198069 88939 RMVar_ID_88939 Human_SNP_ID_64847111 m1A Human chr2 + 27629158 27629158 27629158 TGGTGTTGGGAATGGCGGGATCCGGGAAAACCACTTTTGTACAGGTGACGTACACAGCATGGGTG TGGTGTTGGGAATGGCGGGATCCGGGAAAACCTCTTTTGTACAGGTGACGTACACAGCATGGGTG A T AC074091.2,GPN1 Ensembl:ENSG00000259080,Ensembl:ENSG00000198522 lincRNA,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:27629035..27629175 26863196 MeRIP-seq:(Medium) rs924806822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624173,Human_RBP_ID_19099752,Human_RBP_ID_21893549 Human_Splice_Rec_229843,Human_Splice_Rec_229869,Human_Splice_Rec_229895,Human_Splice_Rec_229907,Human_Splice_Rec_229933 Human_miRNA_ID_2057159 RMVar_hsa_circ_119954,RMVar_hsa_circ_198069 88940 RMVar_ID_88940 Human_SNP_ID_64847307 m1A Human chr2 - 27629744 27629744 27629744 AGAATATTGCACTTAGATTTTCTTCTACCTGAAATATCCACCATGTCCACCTCCAAGATACAACT AGAATATTGCACTTAGATTTTCTTCTACCTGAGATATCCACCATGTCCACCTCCAAGATACAACT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:27629742..27629950 26863196 MeRIP-seq:(Medium) rs1558484596 Functional Loss SNV dbSNP153 33..33 33 - - - 88941 RMVar_ID_88941 Human_SNP_ID_64852648 m1A Human chr2 + 27651465 27651465 27651465 ATTTCCCTCGTCTTGACCATCTGGTGCCTGTTATGCAGTTTAACATTCTGCAGCAATAAAAGTGT ATTTCCCTCGTCTTGACCATCTGGTGCCTGTTCTGCAGTTTAACATTCTGCAGCAATAAAAGTGT A C GPN1 Ensembl:ENSG00000198522 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10201652 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11563,GWAS_ID_11564,GWAS_ID_11565,GWAS_ID_11566,GWAS_ID_11567 88942 RMVar_ID_88942 Human_SNP_ID_64854889 m1A Human chr2 - 27661185 27661185 27661185 CACCATCCATACGATTCAGTTGATTCAGCACAACCGACGTCTTCGCAACCTTATTGCCACAGCTC CACCATCCATACGATTCAGTTGATTCAGCACAGCCGACGTCTTCGCAACCTTATTGCCACAGCTC T C SUPT7L Ensembl:ENSG00000119760 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:27661134..27661325 26863196 MeRIP-seq:(Medium) rs1360470770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_549016,Human_RBP_ID_13845322,Human_RBP_ID_26340791,Human_RBP_ID_27694740 RMVar_hsa_circ_32677,RMVar_hsa_circ_123754,RMVar_hsa_circ_198080 88943 RMVar_ID_88943 Human_SNP_ID_64854914 m1A Human chr2 - 27661266 27661266 27661266 TGACCCACCCCTGCACCAACCCTCAGCCAACAAGCCGAAGCCCCCCACTATGCTGGACATCCCCT TGACCCACCCCTGCACCAACCCTCAGCCAACAGGCCGAAGCCCCCCACTATGCTGGACATCCCCT T C SUPT7L Ensembl:ENSG00000119760 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27661085..27661338 26863196 MeRIP-seq:(Medium) rs903144517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242658,Human_RBP_ID_775453,Human_RBP_ID_828529,Human_RBP_ID_9383432 Human_miRNA_ID_971468 RMVar_hsa_circ_32677,RMVar_hsa_circ_123754,RMVar_hsa_circ_198080 88944 RMVar_ID_88944 Human_SNP_ID_64855447 m1A Human chr2 + 27663445 27663445 27663445 AGGCGCCAATCACAGGGTCCTGAGGTCGCCTGACGTTCAGGGCAGCCGGAAGACGGGGAGGTCTG AGGCGCCAATCACAGGGTCCTGAGGTCGCCTGTCGTTCAGGGCAGCCGGAAGACGGGGAGGTCTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27663394..27663594 26863196 MeRIP-seq:(Medium) rs1215655603 Functional Loss SNV dbSNP153 33..33 33 - - - 88945 RMVar_ID_88945 Human_SNP_ID_64855452 m1A Human chr2 + 27663465 27663465 27663465 TGAGGTCGCCTGACGTTCAGGGCAGCCGGAAGACGGGGAGGTCTGGACCTGAACCGAGACAAGGA TGAGGTCGCCTGACGTTCAGGGCAGCCGGAAGCCGGGGAGGTCTGGACCTGAACCGAGACAAGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27663415..27663613 26863196 MeRIP-seq:(Medium) rs1302907487 Functional Loss SNV dbSNP153 33..33 33 - - - 88946 RMVar_ID_88946 Human_SNP_ID_64855481 m1A Human chr2 + 27663573 27663573 27663573 GCTGTCTGGACCTCGAGAGGCCTGAGGCAAGGATCGCGTCAGACCCCGAAAGCTGGTTTGTTGAT GCTGTCTGGACCTCGAGAGGCCTGAGGCAAGGGTCGCGTCAGACCCCGAAAGCTGGTTTGTTGAT A G SLC4A1AP Ensembl:ENSG00000163798 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:27663326..27663625 26863196 MeRIP-seq:(Medium) rs1172701760 Functional Loss SNV dbSNP153 33..33 33 - - - 88947 RMVar_ID_88947 Human_SNP_ID_64856708 m1A Human chr2 + 27667352 27667352 27667352 TCAGCAGGAAAGGGAGGCCTTTTATATAAAGGATCCCAAAAAGGCTCTCCAAGGCTTTTTTGACC TCAGCAGGAAAGGGAGGCCTTTTATATAAAGGGTCCCAAAAAGGCTCTCCAAGGCTTTTTTGACC A G SLC4A1AP Ensembl:ENSG00000163798 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27667303..27668649 32194978 MeRIP-seq:(Medium) rs1428652376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60080,Human_RBP_ID_1022880,Human_RBP_ID_9383437,Human_RBP_ID_25531466,Human_RBP_ID_26339170 Human_Splice_Rec_230002,Human_Splice_Rec_230003,Human_Splice_Rec_230024,Human_Splice_Rec_230025,Human_Splice_Rec_230046,Human_Splice_Rec_230047,Human_Splice_Rec_230068,Human_Splice_Rec_230069,Human_Splice_Rec_230078,Human_Splice_Rec_230079 RMVar_hsa_circ_25888,RMVar_hsa_circ_76740,RMVar_hsa_circ_28755,RMVar_hsa_circ_72679,RMVar_hsa_circ_356057,RMVar_hsa_circ_198081,RMVar_hsa_circ_113314,RMVar_hsa_circ_198082 88948 RMVar_ID_88948 Human_SNP_ID_64861192 m1A Human chr2 + 27685204 27685204 27685204 GATGGAAGCCTCAGTAGGCCACAGCCAGAGATAGAGCCAGAAGCAGCAGTGCAGGAAATGAGGCC GATGGAAGCCTCAGTAGGCCACAGCCAGAGATGGAGCCAGAAGCAGCAGTGCAGGAAATGAGGCC A G SLC4A1AP Ensembl:ENSG00000163798 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27685080..27685217 26863196 MeRIP-seq:(Medium) rs1428257789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9383441,Human_RBP_ID_23865863,Human_RBP_ID_26339172 Human_Splice_Rec_230015,Human_Splice_Rec_230037,Human_Splice_Rec_230059 RMVar_hsa_circ_366171,RMVar_hsa_circ_59002,RMVar_hsa_circ_198085,RMVar_hsa_circ_79968 88949 RMVar_ID_88949 Human_SNP_ID_64861194 m1A Human chr2 + 27685206 27685206 27685206 TGGAAGCCTCAGTAGGCCACAGCCAGAGATAGAGCCAGAAGCAGCAGTGCAGGAAATGAGGCCTC TGGAAGCCTCAGTAGGCCACAGCCAGAGATAGCGCCAGAAGCAGCAGTGCAGGAAATGAGGCCTC A C SLC4A1AP Ensembl:ENSG00000163798 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr2:27685067..27685250;chr2:27685106..27685225;chr2:27685083..27685250;chr2:27682270..27685245 26863196,32194978 MeRIP-seq:(Medium) rs750941547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9383441,Human_RBP_ID_23865863,Human_RBP_ID_26339172 Human_Splice_Rec_230015,Human_Splice_Rec_230037,Human_Splice_Rec_230059 RMVar_hsa_circ_366171,RMVar_hsa_circ_59002,RMVar_hsa_circ_198085,RMVar_hsa_circ_79968 88950 RMVar_ID_88950 Human_SNP_ID_64907204 m1A Human chr2 + 27890315 27890315 27890315 CACCACTACCACCGCCGCCACCTCCTCTTGCCACTGCCTCTGGGGTTCCCCAGACGCCGCCATCG CACCACTACCACCGCCGCCACCTCCTCTTGCCGCTGCCTCTGGGGTTCCCCAGACGCCGCCATCG A G MRPL33,BABAM2 Ensembl:ENSG00000243147,Ensembl:ENSG00000158019 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27870887..27890424 26863196 MeRIP-seq:(Medium) rs747633256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72708 88951 RMVar_ID_88951 Human_SNP_ID_64907214 m1A Human chr2 + 27890334 27890334 27890334 ACCTCCTCTTGCCACTGCCTCTGGGGTTCCCCAGACGCCGCCATCGCTCAAAGGTGCTGCTGTCC ACCTCCTCTTGCCACTGCCTCTGGGGTTCCCCGGACGCCGCCATCGCTCAAAGGTGCTGCTGTCC A G MRPL33,BABAM2 Ensembl:ENSG00000243147,Ensembl:ENSG00000158019 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:27890158..27890585;chr2:27890220..27890554 26863196 MeRIP-seq:(Medium) rs747552945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72708 88952 RMVar_ID_88952 Human_SNP_ID_64908244 m1A Human chr2 - 27894656 27894656 27894656 ATACCCAGATTTTAAGTCAGTTATCCTCAAACAGTTTGTAGCATCCAGTCCCACTTTTCCATTCC ATACCCAGATTTTAAGTCAGTTATCCTCAAACGGTTTGTAGCATCCAGTCCCACTTTTCCATTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27894557..27894658 32194978 MeRIP-seq:(Medium) rs914339383 Functional Loss SNV dbSNP153 33..33 33 - - - 88953 RMVar_ID_88953 Human_SNP_ID_65021556 m1A Human chr2 + 28392906 28392891 28392907 GGCAGAGCGCTAGGGCTCCGAGCGAACCAGCGAGCGAGCGAACGAGCGGCGCTCGGCGGGGACAG GGCAGAGCGCTAGGGCTC________________CGAGCGAACGAGCGGCGCTCGGCGGGGACAG CCGAGCGAACCAGCGAG C FOSL2 Ensembl:ENSG00000075426 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:28392851..28393124 26863196 MeRIP-seq:(Medium) rs1196860402 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_18421733 88954 RMVar_ID_88954 Human_SNP_ID_65021826 m1A Human chr2 + 28393608 28393600 28393608 CGCGGTGGGGGAGAAACCCAGGAGCGAAGCCCAGAGCCCGCGGCGCGGCCGGCGGACGAACGAGC CGCGGTGGGGGAGAAACCCAGGAGC________GAGCCCGCGGCGCGGCCGGCGGACGAACGAGC CGAAGCCCA C FOSL2 Ensembl:ENSG00000075426 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:28393301..28393700 26863196 MeRIP-seq:(Medium) rs1433626484 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_19001473 88955 RMVar_ID_88955 Human_SNP_ID_65021950 m1A Human chr2 - 28393874 28393874 28393874 GAAAAGAAAGCAAAAGAGGCAGTGGCGGCGAGAAGAGGGCAGGGGTCCGCCCGCGCCGCCAGGTG GAAAAGAAAGCAAAAGAGGCAGTGGCGGCGAGTAGAGGGCAGGGGTCCGCCCGCGCCGCCAGGTG T A AC104695.2 Ensembl:ENSG00000229951 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:28393851..28393875 26863196 MeRIP-seq:(Medium) rs769333900 Functional Loss SNV dbSNP153 33..33 33 - - - 88956 RMVar_ID_88956 Human_SNP_ID_65114320 m1A Human chr2 + 28752107 28752105 28752107 CCGAGAAGCCCTTGTTCCCGCTGCTGGGAAGGAGAGTCTGTGCCGACAAGATGGCGGACGGGGAG CCGAGAAGCCCTTGTTCCCGCTGCTGGGAAG__GAGTCTGTGCCGACAAGATGGCGGACGGGGAG GGA G PPP1CB Ensembl:ENSG00000213639 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:28751727..28776925 26863196 MeRIP-seq:(Medium) rs1218330239 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1022899,Human_RBP_ID_4606436,Human_RBP_ID_6907925,Human_RBP_ID_8201414,Human_RBP_ID_8516983,Human_RBP_ID_8851815,Human_RBP_ID_8942567,Human_RBP_ID_9430023,Human_RBP_ID_13849325,Human_RBP_ID_18193469,Human_RBP_ID_18758786,Human_RBP_ID_22996800,Human_RBP_ID_26338512,Human_RBP_ID_27840008 Human_Splice_Rec_230942,Human_Splice_Rec_230943,Human_Splice_Rec_230948,Human_Splice_Rec_230949,Human_Splice_Rec_230960,Human_Splice_Rec_230961,Human_Splice_Rec_230976,Human_Splice_Rec_230977,Human_Splice_Rec_230991,Human_Splice_Rec_231005 RMVar_hsa_circ_198107,RMVar_hsa_circ_270896,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108 88957 RMVar_ID_88957 Human_SNP_ID_65121024 m1A Human chr2 + 28776858 28776858 28776858 GACTGTTTTATTTATCGTTTGTCAGTACGAGGATGTCGTCCAGGAAAGATTGTGCAGATGACTGA GACTGTTTTATTTATCGTTTGTCAGTACGAGGGTGTCGTCCAGGAAAGATTGTGCAGATGACTGA A G PPP1CB Ensembl:ENSG00000213639 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:28776851..28776900 26863196 MeRIP-seq:(Medium) rs775116467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_829390,Human_RBP_ID_915406,Human_RBP_ID_1585800,Human_RBP_ID_2636010,Human_RBP_ID_4606437,Human_RBP_ID_8234273,Human_RBP_ID_8516994,Human_RBP_ID_8851817,Human_RBP_ID_9259677,Human_RBP_ID_9296408,Human_RBP_ID_13849659,Human_RBP_ID_22452131,Human_RBP_ID_22667153,Human_RBP_ID_23866240,Human_RBP_ID_24377144 Human_Splice_Rec_230934,Human_Splice_Rec_230944,Human_Splice_Rec_230950,Human_Splice_Rec_230954,Human_Splice_Rec_230962,Human_Splice_Rec_230978,Human_Splice_Rec_230992,Human_Splice_Rec_231006 Human_miRNA_ID_2508574 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_270896,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273853,RMVar_hsa_circ_330912,RMVar_hsa_circ_361161,RMVar_hsa_circ_319196,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_198110,RMVar_hsa_circ_198111,RMVar_hsa_circ_198109 88958 RMVar_ID_88958 Human_SNP_ID_65151610 m1A Human chr2 + 28894775 28894775 28894775 TGGGGTCCCTTGCGCCTTCTCCCCGCACAGCCAGGCCTACTTCGCTTTGGCCTCTACCGACGGTC TGGGGTCCCTTGCGCCTTCTCCCCGCACAGCCCGGCCTACTTCGCTTTGGCCTCTACCGACGGTC A C WDR43 Ensembl:ENSG00000163811 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:28894676..28894825 26863410 MeRIP-seq:(Medium) rs1039860010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61622,Human_RBP_ID_4606560,Human_RBP_ID_5502090,Human_RBP_ID_8517048,Human_RBP_ID_8851122,Human_RBP_ID_18443426,Human_RBP_ID_22074723,Human_RBP_ID_22250701,Human_RBP_ID_22451210 88959 RMVar_ID_88959 Human_SNP_ID_65151611 m1A Human chr2 + 28894775 28894775 28894775 TGGGGTCCCTTGCGCCTTCTCCCCGCACAGCCAGGCCTACTTCGCTTTGGCCTCTACCGACGGTC TGGGGTCCCTTGCGCCTTCTCCCCGCACAGCCTGGCCTACTTCGCTTTGGCCTCTACCGACGGTC A T WDR43 Ensembl:ENSG00000163811 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:28894676..28894825 26863410 MeRIP-seq:(Medium) rs1039860010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61622,Human_RBP_ID_4606560,Human_RBP_ID_5502090,Human_RBP_ID_8517048,Human_RBP_ID_8851122,Human_RBP_ID_18443426,Human_RBP_ID_22074723,Human_RBP_ID_22250701,Human_RBP_ID_22451210 88960 RMVar_ID_88960 Human_SNP_ID_65154426 m1A Human chr2 - 28905014 28905014 28905014 CCAGAAGGTCCAAATGAAATCACTTCTCCTCCAGGCCTTCCCAACACTGCTGGAACTCATCTGAC CCAGAAGGTCCAAATGAAATCACTTCTCCTCCGGGCCTTCCCAACACTGCTGGAACTCATCTGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:28905012..28905265 26863196 MeRIP-seq:(Medium) rs528866930 Functional Loss SNV dbSNP153 33..33 33 - - - 88961 RMVar_ID_88961 Human_SNP_ID_65159884 m1A Human chr2 + 28924078 28924078 28924078 ATCATGAGATGCTTACACCTGGGATATTATGCAGGATGTACACTTGTGGAGAATAAGTGGTAATA ATCATGAGATGCTTACACCTGGGATATTATGCGGGATGTACACTTGTGGAGAATAAGTGGTAATA A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:28924041..28924172 26863196 MeRIP-seq:(Medium) rs1444048079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13852037,Human_RBP_ID_22991771 RMVar_hsa_circ_17476,RMVar_hsa_circ_99946,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_39755,RMVar_hsa_circ_198131,RMVar_hsa_circ_25610,RMVar_hsa_circ_97112,RMVar_hsa_circ_198133,RMVar_hsa_circ_21955,RMVar_hsa_circ_198132,RMVar_hsa_circ_198129,RMVar_hsa_circ_198130,RMVar_hsa_circ_348992,RMVar_hsa_circ_374386,RMVar_hsa_circ_319244,RMVar_hsa_circ_322709,RMVar_hsa_circ_269901,RMVar_hsa_circ_111760,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_371162,RMVar_hsa_circ_123945,RMVar_hsa_circ_100306,RMVar_hsa_circ_198141,RMVar_hsa_circ_198143,RMVar_hsa_circ_92247,RMVar_hsa_circ_198144,RMVar_hsa_circ_198142,RMVar_hsa_circ_290035,RMVar_hsa_circ_102130,RMVar_hsa_circ_78685,RMVar_hsa_circ_28552,RMVar_hsa_circ_124310,RMVar_hsa_circ_198150,RMVar_hsa_circ_198151,RMVar_hsa_circ_378894,RMVar_hsa_circ_280712,RMVar_hsa_circ_60896,RMVar_hsa_circ_198152,RMVar_hsa_circ_198154,RMVar_hsa_circ_198153,RMVar_hsa_circ_345651,RMVar_hsa_circ_372543,RMVar_hsa_circ_116837,RMVar_hsa_circ_198156,RMVar_hsa_circ_41471,RMVar_hsa_circ_198157 88962 RMVar_ID_88962 Human_SNP_ID_65166093 m1A Human chr2 + 28946662 28946659 28946662 GAAAGTGAAAAAGATGAGGACGTTGAAGAGGAAGATGAGGATGCCGAAGGAAAAGATGAAGAAAA GAAAGTGAAAAAGATGAGGACGTTGAAGAG___GATGAGGATGCCGAAGGAAAAGATGAAGAAAA GGAA G WDR43 Ensembl:ENSG00000163811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:28946611..28946846 26863196 MeRIP-seq:(Medium) rs1320107519 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_243107,Human_RBP_ID_917803,Human_RBP_ID_2636614,Human_RBP_ID_4606617,Human_RBP_ID_6909001,Human_RBP_ID_8257602,Human_RBP_ID_9347093,Human_RBP_ID_9383457,Human_RBP_ID_13853010,Human_RBP_ID_18443437,Human_RBP_ID_18533578,Human_RBP_ID_20618548,Human_RBP_ID_22076195,Human_RBP_ID_22505507,Human_RBP_ID_22742936,Human_RBP_ID_22991832,Human_RBP_ID_23114984,Human_RBP_ID_23119274,Human_RBP_ID_23866682,Human_RBP_ID_24545778,Human_RBP_ID_24553072,Human_RBP_ID_26339183,Human_RBP_ID_27818372 Human_Splice_Rec_231140,Human_Splice_Rec_231186 RMVar_hsa_circ_198129,RMVar_hsa_circ_116837,RMVar_hsa_circ_198157,RMVar_hsa_circ_104982,RMVar_hsa_circ_79445,RMVar_hsa_circ_198162,RMVar_hsa_circ_82770,RMVar_hsa_circ_198164,RMVar_hsa_circ_106372,RMVar_hsa_circ_198166,RMVar_hsa_circ_198167,RMVar_hsa_circ_198168 88963 RMVar_ID_88963 Human_SNP_ID_65212478 m1A Human chr2 - 29115732 29115732 29115732 ACTGACCTCCCCGCGGGCCCCCAGGGCCGCCCACCCCGGCCCCAACCCCGCCGCCGGCCAGCCCG ACTGACCTCCCCGCGGGCCCCCAGGGCCGCCCCCCCCGGCCCCAACCCCGCCGCCGGCCAGCCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:29115711..29115921 26863196 MeRIP-seq:(Medium) rs913914018 Functional Loss SNV dbSNP153 33..33 33 - - - 88964 RMVar_ID_88964 Human_SNP_ID_65212513 m1A Human chr2 - 29115837 29115836 29115837 TCCGCCCCGAGAAGGCCTCCCCGCGGCCAGCGACACCGGTGCCCACGGGAGGCGGCCGCGGGGCT TCCGCCCCGAGAAGGCCTCCCCGCGGCCAGCG_CACCGGTGCCCACGGGAGGCGGCCGCGGGGCT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:29115827..29115920 26863196 MeRIP-seq:(Medium) rs930378789 Functional Loss DEL dbSNP153 33..33 33 - - - 88965 RMVar_ID_88965 Human_SNP_ID_481532381 m1A Human chr11 + 110220978 110220978 110220978 TAATTTGGGGATAACCATAGGCTACAGAGTCTATATTTTGACTCCTGACAGTTTCTAAGCATGCC TAATTTGGGGATAACCATAGGCTACAGAGTCTGTATTTTGACTCCTGACAGTTTCTAAGCATGCC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:110220897..110220981 26863410 MeRIP-seq:(Medium) rs1448944331 Functional Loss SNV dbSNP153 33..33 33 - - - 88966 RMVar_ID_88966 Human_SNP_ID_481534899 m1A Human chr11 + 110230622 110230621 110230623 ACACACACACACACACACACAGTCTCTCTCTCATTCTCTCTCTCTCTTGCTCAGCCATACAACAC ACACACACACACACACACACAGTCTCTCTCTC__TCTCTCTCTCTCTTGCTCAGCCATACAACAC CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:110230572..110230656 26863196 MeRIP-seq:(Medium) rs112821905 Functional Loss DEL dbSNP153 33..34 33 - - - 88967 RMVar_ID_88967 Human_SNP_ID_481535557 m1A Human chr11 + 110233384 110233384 110233384 TCATCGTGTTCATCATGTTCGTTTTCTGTTGGAGGAATGACTGGTGGTGGTGGAGGTGGAGGGGG TCATCGTGTTCATCATGTTCGTTTTCTGTTGGGGGAATGACTGGTGGTGGTGGAGGTGGAGGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:110233333..110233445 26863196 MeRIP-seq:(Medium) rs1483856623 Functional Loss SNV dbSNP153 33..33 33 - - - 88968 RMVar_ID_88968 Human_SNP_ID_481540873 m1A Human chr11 + 110253897 110253897 110253897 TACATTTAAAAAACTGAGCAGTCTTAAATTTTAGATAGCCTACTCCTATCAATTAAAAGTGAAAG TACATTTAAAAAACTGAGCAGTCTTAAATTTTTGATAGCCTACTCCTATCAATTAAAAGTGAAAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:110253894..110253988 26863196 MeRIP-seq:(Medium) rs748118099 Functional Loss SNV dbSNP153 33..33 33 - - - 88969 RMVar_ID_88969 Human_SNP_ID_481541871 m1A Human chr11 + 110257816 110257816 110257816 AATATTCAGACCCAAAGCATCAACACCTAGCCACAATTCAGTTCCTTTTTTATTTTTTATTTCAA AATATTCAGACCCAAAGCATCAACACCTAGCCCCAATTCAGTTCCTTTTTTATTTTTTATTTCAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:110255384..110257866 32194978 MeRIP-seq:(Medium) rs757983014 Functional Loss SNV dbSNP153 33..33 33 - - - 88970 RMVar_ID_88970 Human_SNP_ID_481546091 m1A Human chr11 - 110272616 110272616 110272616 ACTTATTATTCCTTTTATTTTTATTACAGATCAACGTAAGAGTAACTACAATGGATGCTGAGCTG ACTTATTATTCCTTTTATTTTTATTACAGATCGACGTAAGAGTAACTACAATGGATGCTGAGCTG T C RDX Ensembl:ENSG00000137710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:110272601..110272673 26863196 MeRIP-seq:(Medium) rs533324168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2249955,Human_RBP_ID_3939820,Human_RBP_ID_9362921 Human_Splice_Rec_1295676,Human_Splice_Rec_1295677,Human_Splice_Rec_1295710,Human_Splice_Rec_1295711,Human_Splice_Rec_1295742,Human_Splice_Rec_1295743,Human_Splice_Rec_1295778,Human_Splice_Rec_1295779,Human_Splice_Rec_1295824,Human_Splice_Rec_1295825,Human_Splice_Rec_1295838,Human_Splice_Rec_1295839,Human_Splice_Rec_1295870,Human_Splice_Rec_1295871,Human_Splice_Rec_1295896,Human_Splice_Rec_1295897,Human_Splice_Rec_1295930,Human_Splice_Rec_1295931,Human_Splice_Rec_1295980,Human_Splice_Rec_1295981,Human_Splice_Rec_1295992,Human_Splice_Rec_1295993,Human_Splice_Rec_1295998,Human_Splice_Rec_1295999,Human_Splice_Rec_1296008,Human_Splice_Rec_1296009 RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_153033,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060,RMVar_hsa_circ_319003 88971 RMVar_ID_88971 Human_SNP_ID_481567835 m1A Human chr11 - 110355267 110355267 110355267 ACACAACCCTCTATTGTACTCTTATCCCTCCTAGCCGACTCCGACCCTGTGTTCCATGAGGAGGC ACACAACCCTCTATTGTACTCTTATCCCTCCTGGCCGACTCCGACCCTGTGTTCCATGAGGAGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:110355229..110355340 26863196 MeRIP-seq:(Medium) rs1473094258 Functional Loss SNV dbSNP153 33..33 33 - - - 88972 RMVar_ID_88972 Human_SNP_ID_481586675 m1A Human chr11 + 110429991 110429991 110429991 CGGCGCGGTGCTTCCAGCAGGGTCTCTCCGCCACTCCAGCCCCGCGCCCCTCGCCGCGGCCCTCG CGGCGCGGTGCTTCCAGCAGGGTCTCTCCGCCGCTCCAGCCCCGCGCCCCTCGCCGCGGCCCTCG A G FDX1 Ensembl:ENSG00000137714 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:110429931..110430086 26863196 MeRIP-seq:(Medium) rs1417258311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185372,Human_RBP_ID_5488999 88973 RMVar_ID_88973 Human_SNP_ID_481586676 m1A Human chr11 + 110429991 110429991 110429991 CGGCGCGGTGCTTCCAGCAGGGTCTCTCCGCCACTCCAGCCCCGCGCCCCTCGCCGCGGCCCTCG CGGCGCGGTGCTTCCAGCAGGGTCTCTCCGCCTCTCCAGCCCCGCGCCCCTCGCCGCGGCCCTCG A T FDX1 Ensembl:ENSG00000137714 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:110429931..110430086 26863196 MeRIP-seq:(Medium) rs1417258311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185372,Human_RBP_ID_5488999 88974 RMVar_ID_88974 Human_SNP_ID_481586679 m1A Human chr11 - 110430009 110429997 110430009 AGCTGCGGCGCAGACGCCCGAGGGCCGCGGCGAGGGGCGCGGGGCTGGAGTGGCGGAGAGACCCT AGCTGCGGCGCAGACGCCCGAGGGCCGCGGCG____________CTGGAGTGGCGGAGAGACCCT GCCCCGCGCCCCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:110429965..110430129 26863196 MeRIP-seq:(Medium) rs1246550095 Functional Loss DEL dbSNP153 33..44 33 - - - 88975 RMVar_ID_88975 Human_SNP_ID_481809562 m1A Human chr11 + 111358424 111358422 111358424 CCTCACACACATACTCTCTCACACACACGCTCACACTCTCACACTCACTCTCACACACACACACT CCTCACACACATACTCTCTCACACACACGCT__CACTCTCACACTCACTCTCACACACACACACT TCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111358342..111358461 26863196 MeRIP-seq:(Medium) rs1565360806 Functional Loss DEL dbSNP153 32..33 33 - - - 88976 RMVar_ID_88976 Human_SNP_ID_481809565 m1A Human chr11 + 111358424 111358424 111358424 CCTCACACACATACTCTCTCACACACACGCTCACACTCTCACACTCACTCTCACACACACACACT CCTCACACACATACTCTCTCACACACACGCTCTCACTCTCACACTCACTCTCACACACACACACT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111358342..111358461 26863196 MeRIP-seq:(Medium) rs1262151336 Functional Loss SNV dbSNP153 33..33 33 - - - 88977 RMVar_ID_88977 Human_SNP_ID_481809566 m1A Human chr11 - 111358428 111358426 111358428 AGAGAGTGTGTGTGTGTGAGAGTGAGTGTGAGAGTGTGAGCGTGTGTGTGAGAGAGTATGTGTGT AGAGAGTGTGTGTGTGTGAGAGTGAGTGTGAG__TGTGAGCGTGTGTGTGAGAGAGTATGTGTGT ACT A POU2AF1 Ensembl:ENSG00000110777 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:111358321..111358476 26863196 MeRIP-seq:(Medium) rs776164484 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_365025 88978 RMVar_ID_88978 Human_SNP_ID_481809572 m1A Human chr11 - 111358428 111358428 111358428 AGAGAGTGTGTGTGTGTGAGAGTGAGTGTGAGAGTGTGAGCGTGTGTGTGAGAGAGTATGTGTGT AGAGAGTGTGTGTGTGTGAGAGTGAGTGTGAGTGTGTGAGCGTGTGTGTGAGAGAGTATGTGTGT T A POU2AF1 Ensembl:ENSG00000110777 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:111358321..111358476 26863196 MeRIP-seq:(Medium) rs117390921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365025 88979 RMVar_ID_88979 Human_SNP_ID_481851883 m1A Human chr11 + 111540925 111540925 111540925 TGGGGCTGCGGGCCGCGACGGGTCGCCTGCTGAGTGGTGAGTGCGCGCGCTGGGGCGGGGGCTGG TGGGGCTGCGGGCCGCGACGGGTCGCCTGCTGCGTGGTGAGTGCGCGCGCTGGGGCGGGGGCTGG A C LAYN Ensembl:ENSG00000204381 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:111540801..111541456 32194978 MeRIP-seq:(Medium) rs747546021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1296555,Human_Splice_Rec_1296565,Human_Splice_Rec_1296573,Human_Splice_Rec_1296585,Human_Splice_Rec_1296599,Human_Splice_Rec_1296607 88980 RMVar_ID_88980 Human_SNP_ID_481873068 m1A Human chr11 - 111631460 111631460 111631460 CAGCAACTCTTACATGCATTTCATCTTCCACCATTCTAATCCTCAACCTGGGCCATTCATTCATA CAGCAACTCTTACATGCATTTCATCTTCCACCCTTCTAATCCTCAACCTGGGCCATTCATTCATA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111631455..111631584 26863196 MeRIP-seq:(Medium) rs955201256 Functional Loss SNV dbSNP153 33..33 33 - - - 88981 RMVar_ID_88981 Human_SNP_ID_481879978 m1A Human chr11 + 111663470 111663470 111663470 ATGCAGGGAGGCGTGGTGAGGCATGGGAAGGGACAGGATATGGTTGAGATCACATGGGGTCTAAT ATGCAGGGAGGCGTGGTGAGGCATGGGAAGGGGCAGGATATGGTTGAGATCACATGGGGTCTAAT A G SIK2 Ensembl:ENSG00000170145 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:111663420..111663549 26863196 MeRIP-seq:(Medium) rs990298652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18932921 RMVar_hsa_circ_153045,RMVar_hsa_circ_369876 88982 RMVar_ID_88982 Human_SNP_ID_481892369 m1A Human chr11 + 111720577 111720577 111720577 TGTTCAGAGGGACCTGAACTTTCTGGAAGACAACCCTTCCCTTAAGGACATCATGTTAGCCAATC TGTTCAGAGGGACCTGAACTTTCTGGAAGACAGCCCTTCCCTTAAGGACATCATGTTAGCCAATC A G SIK2 Ensembl:ENSG00000170145 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:111720490..111720582 26863410 MeRIP-seq:(Medium) rs1219629432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17789678,Human_RBP_ID_18525747 Human_Splice_Rec_1296662,Human_Splice_Rec_1296674 Human_miRNA_ID_726057 RMVar_hsa_circ_14181 88983 RMVar_ID_88983 Human_SNP_ID_481893253 m1A Human chr11 - 111723801 111723792 111723802 GGGGTGGTGGCGGTGGCGGCTGCTGCTGCTGTAGCTGCGTGGGCAGAGGAGGAGCAGCCCGGGGA GGGGTGGTGGCGGTGGCGGCTGCTGCTGCTG__________GGCAGAGGAGGAGCAGCCCGGGGA CCACGCAGCTA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:111723751..111724000 26863196 MeRIP-seq:(Medium) rs1162650424 Functional Loss DEL dbSNP153 32..41 33 - - - 88984 RMVar_ID_88984 Human_SNP_ID_481893261 m1A Human chr11 - 111723801 111723801 111723801 GGGGTGGTGGCGGTGGCGGCTGCTGCTGCTGTAGCTGCGTGGGCAGAGGAGGAGCAGCCCGGGGA GGGGTGGTGGCGGTGGCGGCTGCTGCTGCTGTGGCTGCGTGGGCAGAGGAGGAGCAGCCCGGGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:111723751..111724000 26863196 MeRIP-seq:(Medium) rs1473209531 Functional Loss SNV dbSNP153 33..33 33 - - - 88985 RMVar_ID_88985 Human_SNP_ID_481903813 m1A Human chr11 + 111765377 111765377 111765377 GGGCAATTGTTGATAACTTCTTAATACTGTTGAGTCGGAGCTTCAGAAAAGAAAGTAGAAAGAAG GGGCAATTGTTGATAACTTCTTAATACTGTTGCGTCGGAGCTTCAGAAAAGAAAGTAGAAAGAAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:111765326..111765844 26863196 MeRIP-seq:(Medium) rs1555052723 Functional Loss SNV dbSNP153 33..33 33 - - - 88986 RMVar_ID_88986 Human_SNP_ID_481903818 m1A Human chr11 - 111765386 111765385 111765386 TACATTGTTCTTCTTTCTACTTTCTTTTCTGAAGCTCCGACTCAACAGTATTAAGAAGTTATCAA TACATTGTTCTTCTTTCTACTTTCTTTTCTGA_GCTCCGACTCAACAGTATTAAGAAGTTATCAA CT C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111765358..111765424 26863196 MeRIP-seq:(Medium) rs781989131 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_30690,Human_RBP_ID_18972754,Human_RBP_ID_22643835 Human_Splice_Rec_1296677,Human_Splice_Rec_1296737,Human_Splice_Rec_1296765,Human_Splice_Rec_1296793,Human_Splice_Rec_1296819,Human_Splice_Rec_1296859,Human_Splice_Rec_1296865 RMVar_hsa_circ_98866,RMVar_hsa_circ_153051 88987 RMVar_ID_88987 Human_SNP_ID_481903820 m1A Human chr11 - 111765386 111765386 111765386 TACATTGTTCTTCTTTCTACTTTCTTTTCTGAAGCTCCGACTCAACAGTATTAAGAAGTTATCAA TACATTGTTCTTCTTTCTACTTTCTTTTCTGAGGCTCCGACTCAACAGTATTAAGAAGTTATCAA T C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111765358..111765424 26863196 MeRIP-seq:(Medium) rs1365022267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30690,Human_RBP_ID_18972754,Human_RBP_ID_22643835 Human_Splice_Rec_1296677,Human_Splice_Rec_1296737,Human_Splice_Rec_1296765,Human_Splice_Rec_1296793,Human_Splice_Rec_1296819,Human_Splice_Rec_1296859,Human_Splice_Rec_1296865 RMVar_hsa_circ_98866,RMVar_hsa_circ_153051 88988 RMVar_ID_88988 Human_SNP_ID_481904185 m1A Human chr11 - 111766329 111766329 111766329 ATGGCGGGCGCATCAGAGCTCGGGACCGGCCCAGGAGCAGCGGGTGGAGATGGAGATGATTCGCT ATGGCGGGCGCATCAGAGCTCGGGACCGGCCCTGGAGCAGCGGGTGGAGATGGAGATGATTCGCT T A PPP2R1B Ensembl:ENSG00000137713 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:111766195..111766391;chr11:111766251..111766389;chr11:111766253..111766375 26863196 MeRIP-seq:(Medium) rs782156543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24557309 Human_Splice_Rec_1296675,Human_Splice_Rec_1296705,Human_Splice_Rec_1296735,Human_Splice_Rec_1296763,Human_Splice_Rec_1296791,Human_Splice_Rec_1296817,Human_Splice_Rec_1296857 RMVar_hsa_circ_98866,RMVar_hsa_circ_153051 88989 RMVar_ID_88989 Human_SNP_ID_481904307 m1A Human chr11 + 111766440 111766440 111766440 AGGCCCCGCCCCGCGCCCAGGCAGTAGGGACGAAGGCCGCCACGCTGGTTTAGCCGAAGTTGGGG AGGCCCCGCCCCGCGCCCAGGCAGTAGGGACGCAGGCCGCCACGCTGGTTTAGCCGAAGTTGGGG A C lnc-SIK2-3,lnc-SIK2-3:2 RNACentral:URS0000D5C655,RNACentral:URS0000D5CE9D lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:111766371..111766508 26863196 MeRIP-seq:(Medium) rs1167643618 Functional Loss SNV dbSNP153 33..33 33 - - - 88990 RMVar_ID_88990 Human_SNP_ID_481904308 m1A Human chr11 + 111766440 111766440 111766440 AGGCCCCGCCCCGCGCCCAGGCAGTAGGGACGAAGGCCGCCACGCTGGTTTAGCCGAAGTTGGGG AGGCCCCGCCCCGCGCCCAGGCAGTAGGGACGTAGGCCGCCACGCTGGTTTAGCCGAAGTTGGGG A T lnc-SIK2-3,lnc-SIK2-3:2 RNACentral:URS0000D5C655,RNACentral:URS0000D5CE9D lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:111766371..111766508 26863196 MeRIP-seq:(Medium) rs1167643618 Functional Loss SNV dbSNP153 33..33 33 - - - 88991 RMVar_ID_88991 Human_SNP_ID_481912404 m1A Human chr11 + 111802059 111802058 111802059 ATTACTACTGCAGTTCTGGCAATGTCTTGAACACCCATCCATGATCCTACCACCTTTCACTGTCT ATTACTACTGCAGTTCTGGCAATGTCTTGAAC_CCCATCCATGATCCTACCACCTTTCACTGTCT CA C lnc-SIK2-2 RNACentral:URS0000EABD37 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:111802057..111802141 26863196 MeRIP-seq:(Medium) rs782491994 Functional Loss DEL dbSNP153 33..33 33 - - - 88992 RMVar_ID_88992 Human_SNP_ID_481913975 m1A Human chr11 - 111808756 111808756 111808756 AAACAGACAGTTGGAGTTAAGGAGATCCAGGGAGGCCTGGTGAGCAGAGCCCAGGAGCCAGGAGG AAACAGACAGTTGGAGTTAAGGAGATCCAGGGTGGCCTGGTGAGCAGAGCCCAGGAGCCAGGAGG T A AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:111808752..111808869 26863196 MeRIP-seq:(Medium) rs1323919868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40805,RMVar_hsa_circ_153061,RMVar_hsa_circ_57394 88993 RMVar_ID_88993 Human_SNP_ID_481914252 m1A Human chr11 + 111809752 111809752 111809752 TGTTTCTCTCATGGTGTCCAAATCCACTAAATAATGGCATTTACTGATATCAATCTGAAATGGAG TGTTTCTCTCATGGTGTCCAAATCCACTAAATGATGGCATTTACTGATATCAATCTGAAATGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:111809701..111814651 26863196 MeRIP-seq:(Medium) rs1163813425 Functional Loss SNV dbSNP153 33..33 33 - - - 88994 RMVar_ID_88994 Human_SNP_ID_481914257 m1A Human chr11 + 111809772 111809772 111809772 AATCCACTAAATAATGGCATTTACTGATATCAATCTGAAATGGAGAAAGGCCAACTCTTCATTAG AATCCACTAAATAATGGCATTTACTGATATCACTCTGAAATGGAGAAAGGCCAACTCTTCATTAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111809676..111809799 26863196 MeRIP-seq:(Medium) rs12575909 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 88995 RMVar_ID_88995 Human_SNP_ID_481914258 m1A Human chr11 + 111809772 111809772 111809772 AATCCACTAAATAATGGCATTTACTGATATCAATCTGAAATGGAGAAAGGCCAACTCTTCATTAG AATCCACTAAATAATGGCATTTACTGATATCAGTCTGAAATGGAGAAAGGCCAACTCTTCATTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111809676..111809799 26863196 MeRIP-seq:(Medium) rs12575909 Functional Loss SNV dbSNP153 33..33 33 - - - 88996 RMVar_ID_88996 Human_SNP_ID_481931038 m1A Human chr11 - 111879054 111879054 111879054 TCGCCGCCGCTCTGAGCGAAACCCTGGATCAGAGCACTCAACTTACCGCCACCTGCCTCCAGCGC TCGCCGCCGCTCTGAGCGAAACCCTGGATCAGGGCACTCAACTTACCGCCACCTGCCTCCAGCGC T C AP001781.2,FDXACB1 Ensembl:ENSG00000258529,Ensembl:ENSG00000255561 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111879020..111879139 26863196 MeRIP-seq:(Medium) rs531261233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1297117,Human_Splice_Rec_1297169,Human_Splice_Rec_1297177 88997 RMVar_ID_88997 Human_SNP_ID_481966157 m1A Human chr11 - 112025483 112025483 112025483 ATGGGGCTACATTCTGAGCCCGTCGCGCACAGACGCGCCACATAGTGCCACCAACCCCCCACACC ATGGGGCTACATTCTGAGCCCGTCGCGCACAGGCGCGCCACATAGTGCCACCAACCCCCCACACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112025157..112025599 26863196 MeRIP-seq:(Medium) rs782019892 Functional Loss SNV dbSNP153 33..33 33 - - - 88998 RMVar_ID_88998 Human_SNP_ID_481969806 m1A Human chr11 - 112037336 112037336 112037336 CTACAATGATACAGAGTGGGGTTCCTAGAGGGACATCTCTTGTGCCTTCAGGGACCAGGATTTTT CTACAATGATACAGAGTGGGGTTCCTAGAGGGGCATCTCTTGTGCCTTCAGGGACCAGGATTTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112037276..112037490 26863196 MeRIP-seq:(Medium) rs1555180591 Functional Loss SNV dbSNP153 33..33 33 - - - 88999 RMVar_ID_88999 Human_SNP_ID_481969818 m1A Human chr11 + 112037369 112037369 112037369 CCCTCTAGGAACCCCACTCTGTATCATTGTAGAAAAAGAGGCAGATATATCAGCATTTGCTGACT CCCTCTAGGAACCCCACTCTGTATCATTGTAGGAAAAGAGGCAGATATATCAGCATTTGCTGACT A G DLAT Ensembl:ENSG00000150768 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:112037233..112037496 26863196 MeRIP-seq:(Medium) rs1555180596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_388823,Human_RBP_ID_21883778,Human_RBP_ID_24364471 Human_Splice_Rec_1297512,Human_Splice_Rec_1297513,Human_Splice_Rec_1297538,Human_Splice_Rec_1297539,Human_Splice_Rec_1297582,Human_Splice_Rec_1297583 RMVar_hsa_circ_77824,RMVar_hsa_circ_110373,RMVar_hsa_circ_153085,RMVar_hsa_circ_364755,RMVar_hsa_circ_47304,RMVar_hsa_circ_153088,RMVar_hsa_circ_153091,RMVar_hsa_circ_153089,RMVar_hsa_circ_337521,RMVar_hsa_circ_359660,RMVar_hsa_circ_374137,RMVar_hsa_circ_355529,RMVar_hsa_circ_301091,RMVar_hsa_circ_324371,RMVar_hsa_circ_286768,RMVar_hsa_circ_279757,RMVar_hsa_circ_297445,RMVar_hsa_circ_329386,RMVar_hsa_circ_281540,RMVar_hsa_circ_153092,RMVar_hsa_circ_153090 89000 RMVar_ID_89000 Human_SNP_ID_481969835 m1A Human chr11 + 112037410 112037410 112037410 CAGATATATCAGCATTTGCTGACTATAGGCCAACCGAAGTAACAGATTTAAAACCACAAGTGCCA CAGATATATCAGCATTTGCTGACTATAGGCCAGCCGAAGTAACAGATTTAAAACCACAAGTGCCA A G DLAT Ensembl:ENSG00000150768 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:112037361..112037501 26863196 MeRIP-seq:(Medium) rs1283333530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30989,Human_RBP_ID_388824 Human_Splice_Rec_1297513,Human_Splice_Rec_1297539,Human_Splice_Rec_1297583 RMVar_hsa_circ_77824,RMVar_hsa_circ_110373,RMVar_hsa_circ_153085,RMVar_hsa_circ_364755,RMVar_hsa_circ_47304,RMVar_hsa_circ_153088,RMVar_hsa_circ_153091,RMVar_hsa_circ_153089,RMVar_hsa_circ_337521,RMVar_hsa_circ_359660,RMVar_hsa_circ_374137,RMVar_hsa_circ_355529,RMVar_hsa_circ_301091,RMVar_hsa_circ_324371,RMVar_hsa_circ_286768,RMVar_hsa_circ_279757,RMVar_hsa_circ_297445,RMVar_hsa_circ_329386,RMVar_hsa_circ_281540,RMVar_hsa_circ_153092,RMVar_hsa_circ_153090 89001 RMVar_ID_89001 Human_SNP_ID_481970301 m1A Human chr11 - 112039399 112039399 112039399 CTTTATAAAGTCCATTCTATAGAAACAGATTTACCTTTTACTTGTGTAAGATCAATCCCTTTCTC CTTTATAAAGTCCATTCTATAGAAACAGATTTGCCTTTTACTTGTGTAAGATCAATCCCTTTCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:112039351..112039400 32194978 MeRIP-seq:(Medium) rs782070173 Functional Loss SNV dbSNP153 33..33 33 - - - 89002 RMVar_ID_89002 Human_SNP_ID_481978744 m1A Human chr11 + 112074440 112074440 112074440 GGTTACCGGGAGCTCCGAGGCCGCTGGGGAACAGGGATCCCGGTGACAAAGATGGGGATATTTCC GGTTACCGGGAGCTCCGAGGCCGCTGGGGAACGGGGATCCCGGTGACAAAGATGGGGATATTTCC A G NKAPD1 Ensembl:ENSG00000150776 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:112074406..112074561 32194978 MeRIP-seq:(Medium) rs1468886776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4186816,Human_RBP_ID_8344545 89003 RMVar_ID_89003 Human_SNP_ID_481980751 m1A Human chr11 + 112082628 112082628 112082628 AACAGAAGAAAAGCAAAAAGGAAGCCACAGATATAACAGCAGATTCCTCGAGTGAGTTCTCAGAA AACAGAAGAAAAGCAAAAAGGAAGCCACAGATGTAACAGCAGATTCCTCGAGTGAGTTCTCAGAA A G NKAPD1 Ensembl:ENSG00000150776 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112082578..112082668 26863196 MeRIP-seq:(Medium) rs201641008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_388900,Human_RBP_ID_985773,Human_RBP_ID_6043544 89004 RMVar_ID_89004 Human_SNP_ID_481981820 m1A Human chr11 - 112086653 112086653 112086653 GCGCCTGGTGGCCGCCGAGCAGCAGAAGGCGCAGTTTACTGCACAGGTGCGGGGACGGGGAGGGT GCGCCTGGTGGCCGCCGAGCAGCAGAAGGCGCGGTTTACTGCACAGGTGCGGGGACGGGGAGGGT T C TIMM8B Ensembl:ENSG00000150779 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:112086080..112086652 32194978 MeRIP-seq:(Medium) rs1306370876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184409,Human_RBP_ID_22433928 Human_Splice_Rec_1297745,Human_Splice_Rec_1297747,Human_Splice_Rec_1297751,Human_Splice_Rec_1297753 89005 RMVar_ID_89005 Human_SNP_ID_481981857 m1A Human chr11 - 112086706 112086706 112086706 AGCCTGAGGCGAACAATGGCGGAGCTGGGCGAAGCCGATGAAGCGGAGTTGCAGCGCCTGGTGGC AGCCTGAGGCGAACAATGGCGGAGCTGGGCGAGGCCGATGAAGCGGAGTTGCAGCGCCTGGTGGC T C TIMM8B Ensembl:ENSG00000150779 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:112086626..112086775 26863196 MeRIP-seq:(Medium) rs577227947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227779,Human_RBP_ID_388975,Human_RBP_ID_751377,Human_RBP_ID_1454097,Human_RBP_ID_4184409,Human_RBP_ID_22433928 Human_Splice_Rec_1297745,Human_Splice_Rec_1297747,Human_Splice_Rec_1297751,Human_Splice_Rec_1297753 89006 RMVar_ID_89006 Human_SNP_ID_481981858 m1A Human chr11 - 112086706 112086706 112086706 AGCCTGAGGCGAACAATGGCGGAGCTGGGCGAAGCCGATGAAGCGGAGTTGCAGCGCCTGGTGGC AGCCTGAGGCGAACAATGGCGGAGCTGGGCGACGCCGATGAAGCGGAGTTGCAGCGCCTGGTGGC T G TIMM8B Ensembl:ENSG00000150779 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:112086626..112086775 26863196 MeRIP-seq:(Medium) rs577227947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227779,Human_RBP_ID_388975,Human_RBP_ID_751377,Human_RBP_ID_1454097,Human_RBP_ID_4184409,Human_RBP_ID_22433928 Human_Splice_Rec_1297745,Human_Splice_Rec_1297747,Human_Splice_Rec_1297751,Human_Splice_Rec_1297753 89007 RMVar_ID_89007 Human_SNP_ID_481981985 m1A Human chr11 + 112086923 112086923 112086923 GAGCCCTCAGGAACGAGATGGCGGTTCTCTGGAGGCTGAGTGCCGTTTGCGGTGCCCTAGGAGGC GAGCCCTCAGGAACGAGATGGCGGTTCTCTGGGGGCTGAGTGCCGTTTGCGGTGCCCTAGGAGGC A G AP002884.2,SDHD Ensembl:ENSG00000255292,Ensembl:ENSG00000204370 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:112086872..112087870 26863196 MeRIP-seq:(Medium) rs11547889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866171,Human_RBP_ID_4185379,Human_RBP_ID_5313831,Human_RBP_ID_8774511,Human_RBP_ID_9321778,Human_RBP_ID_22433929,Human_RBP_ID_22895489,Human_RBP_ID_23207094,Human_RBP_ID_23486324 Human_Splice_Rec_1297757,Human_Splice_Rec_1297763,Human_Splice_Rec_1297767,Human_Splice_Rec_1297773,Human_Splice_Rec_1297777,Human_Splice_Rec_1297781,Human_Splice_Rec_1297785,Human_Splice_Rec_1297789,Human_Splice_Rec_1297791,Human_Splice_Rec_1297799,Human_Splice_Rec_1297805,Human_Splice_Rec_1297811 Clinvar_Rec_501 89008 RMVar_ID_89008 Human_SNP_ID_481982013 m1A Human chr11 + 112086958 112086958 112086958 CTGAGTGCCGTTTGCGGTGCCCTAGGAGGCCGAGGTGAGGGGTCTTCCCACCCTGAGGTGCTTAG CTGAGTGCCGTTTGCGGTGCCCTAGGAGGCCGCGGTGAGGGGTCTTCCCACCCTGAGGTGCTTAG A C AP002884.2,SDHD Ensembl:ENSG00000255292,Ensembl:ENSG00000204370 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:112086876..112086975 32194978 MeRIP-seq:(Medium) rs199890548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866171,Human_RBP_ID_4185379,Human_RBP_ID_5313831,Human_RBP_ID_8774511,Human_RBP_ID_9276071,Human_RBP_ID_9321778,Human_RBP_ID_22433235,Human_RBP_ID_22895489,Human_RBP_ID_23207095 Human_Splice_Rec_1297757,Human_Splice_Rec_1297763,Human_Splice_Rec_1297767,Human_Splice_Rec_1297773,Human_Splice_Rec_1297777,Human_Splice_Rec_1297781,Human_Splice_Rec_1297785,Human_Splice_Rec_1297789,Human_Splice_Rec_1297791,Human_Splice_Rec_1297799,Human_Splice_Rec_1297805,Human_Splice_Rec_1297811 Clinvar_Rec_502 89009 RMVar_ID_89009 Human_SNP_ID_481982235 m1A Human chr11 + 112087855 112087855 112087855 GTTCTTATGATCATCCTAATGACTCTTTCCTCAGCTCTGTTGCTTCGAACTCCAGTGGTCAGACC GTTCTTATGATCATCCTAATGACTCTTTCCTCCGCTCTGTTGCTTCGAACTCCAGTGGTCAGACC A C AP002884.2,SDHD Ensembl:ENSG00000255292,Ensembl:ENSG00000204370 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:112087851..112093127 32194978 MeRIP-seq:(Medium) rs778969755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185380 89010 RMVar_ID_89010 Human_SNP_ID_482015878 m1A Human chr11 - 112226461 112226461 112226461 CGGCGGGACACTTGTGCCTGGCAGCGACGGCCACCACCTTCCGTGCTCATCTTCCCGGCGCTGTC CGGCGGGACACTTGTGCCTGGCAGCGACGGCCGCCACCTTCCGTGCTCATCTTCCCGGCGCTGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:112226364..112226630 26863196 MeRIP-seq:(Medium) rs1275853008 Functional Loss SNV dbSNP153 33..33 33 - - - 89011 RMVar_ID_89011 Human_SNP_ID_482016544 m1A Human chr11 + 112228644 112228644 112228644 AGAAAACTTGAAACTGTTTGGGAAATGCAACAATCCAAATGGCCATGGGCACAATTATAAAGGTG AGAAAACTTGAAACTGTTTGGGAAATGCAACAGTCCAAATGGCCATGGGCACAATTATAAAGGTG A G PTS Ensembl:ENSG00000150787 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:112228529..112228650 26863196 MeRIP-seq:(Medium) rs753372875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32420,Human_RBP_ID_389005,Human_RBP_ID_865515,Human_RBP_ID_1775465,Human_RBP_ID_5341869,Human_RBP_ID_8344598,Human_RBP_ID_19054280,Human_RBP_ID_23486420 Human_Splice_Rec_1298106,Human_Splice_Rec_1298107,Human_Splice_Rec_1298114,Human_Splice_Rec_1298116,Human_Splice_Rec_1298117,Human_Splice_Rec_1298128,Human_Splice_Rec_1298129,Human_Splice_Rec_1298138,Human_Splice_Rec_1298139,Human_Splice_Rec_1298144,Human_Splice_Rec_1298145 RMVar_hsa_circ_352942 89012 RMVar_ID_89012 Human_SNP_ID_482023274 m1A Human chr11 - 112254482 112254478 112254482 ACACCACACACACTCATGCCACACACACATACATACCACATGCACCACTCACACCACACACACCA ACACCACACACACTCATGCCACACACACATAC____CACATGCACCACTCACACCACACACACCA GGTAT G PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112254288..112254509 26863196 MeRIP-seq:(Medium) rs1411224276 Functional Loss DEL dbSNP153 33..36 33 - - - 89013 RMVar_ID_89013 Human_SNP_ID_482023277 m1A Human chr11 + 112254485 112254483 112254485 TGTGTGTGGTGTGAGTGGTGCATGTGGTATGTATGTGTGTGTGGCATGAGTGTGTGTGGTGTGTG TGTGTGTGGTGTGAGTGGTGCATGTGGTATG__TGTGTGTGTGGCATGAGTGTGTGTGGTGTGTG GTA G PTS Ensembl:ENSG00000150787 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:112254266..112254515 26863196 MeRIP-seq:(Medium) rs1422229639 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5282350,Human_RBP_ID_27836688 89014 RMVar_ID_89014 Human_SNP_ID_482023278 m1A Human chr11 + 112254485 112254485 112254485 TGTGTGTGGTGTGAGTGGTGCATGTGGTATGTATGTGTGTGTGGCATGAGTGTGTGTGGTGTGTG TGTGTGTGGTGTGAGTGGTGCATGTGGTATGTGTGTGTGTGTGGCATGAGTGTGTGTGGTGTGTG A G PTS Ensembl:ENSG00000150787 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:112254266..112254515 26863196 MeRIP-seq:(Medium) rs1369755897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5282350,Human_RBP_ID_27836688 89015 RMVar_ID_89015 Human_SNP_ID_482023425 m1A Human chr11 - 112254719 112254717 112254720 ACACACAGCACACACACACCACACACACACTCACAACACACACATACATACCACACACACCACAC ACACACAGCACACACACACCACACACACACT___AACACACACATACATACCACACACACCACAC TGTG T PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112254571..112254769 26863196 MeRIP-seq:(Medium) rs1330910320 Functional Loss DEL dbSNP153 32..34 33 - - - 89016 RMVar_ID_89016 Human_SNP_ID_482023571 m1A Human chr11 - 112254941 112254939 112254941 ACACTCACATACATATCACACACACCACACACACGCTCACAGCACACACACATACATACCCCACA ACACTCACATACATATCACACACACCACACAC__GCTCACAGCACACACACATACATACCCCACA CGT C PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:112254891..112254995 26863196 MeRIP-seq:(Medium) rs568319567 Functional Loss DEL dbSNP153 33..34 33 - - - 89017 RMVar_ID_89017 Human_SNP_ID_482023575 m1A Human chr11 - 112254941 112254941 112254941 ACACTCACATACATATCACACACACCACACACACGCTCACAGCACACACACATACATACCCCACA ACACTCACATACATATCACACACACCACACACGCGCTCACAGCACACACACATACATACCCCACA T C PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:112254891..112254995 26863196 MeRIP-seq:(Medium) rs1255040056 Functional Loss SNV dbSNP153 33..33 33 - - - 89018 RMVar_ID_89018 Human_SNP_ID_482023588 m1A Human chr11 - 112254963 112254962 112254964 CACCACATATCACACACACACCACACTCACATACATATCACACACACCACACACACGCTCACAGC CACCACATATCACACACACACCACACTCACA__CATATCACACACACCACACACACGCTCACAGC GTA G PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:112254843..112255130 26863196 MeRIP-seq:(Medium) rs550942024 Functional Loss DEL dbSNP153 32..33 33 - - - 89019 RMVar_ID_89019 Human_SNP_ID_482389281 m1A Human chr11 - 113773647 113773647 113773647 TCCCGTCTTGGCCATGGCCTCGTTCGTGACAGAAGTTTTGGCACACTCCGGGAGGCTGGAAAAGG TCCCGTCTTGGCCATGGCCTCGTTCGTGACAGGAGTTTTGGCACACTCCGGGAGGCTGGAAAAGG T C ZW10 Ensembl:ENSG00000086827 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:113773180..113773691 26863196 MeRIP-seq:(Medium) rs1565290960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29605,Human_RBP_ID_389112,Human_RBP_ID_4185385 Human_Splice_Rec_1299511,Human_Splice_Rec_1299541,Human_Splice_Rec_1299571 Human_miRNA_ID_1960678,Human_miRNA_ID_2032495,Human_miRNA_ID_2887433,Human_miRNA_ID_2910354 RMVar_hsa_circ_109625,RMVar_hsa_circ_153149 89020 RMVar_ID_89020 Human_SNP_ID_482521756 m1A Human chr11 + 114295884 114295884 114295884 GGTGAAGCTGCAGTTGCCTAGGGCAGGGATGGAGAGAGAGTCTGGGCATGAGGAGAGGGTCTCGG GGTGAAGCTGCAGTTGCCTAGGGCAGGGATGGGGAGAGAGTCTGGGCATGAGGAGAGGGTCTCGG A G NNMT Ensembl:ENSG00000166741 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:114295776..114295950;chr11:114295735..114295905;chr11:114295730..114295893 26863196 MeRIP-seq:(Medium) rs979514212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118280,RMVar_hsa_circ_80088,RMVar_hsa_circ_110154,RMVar_hsa_circ_153179,RMVar_hsa_circ_153180,RMVar_hsa_circ_153181 89021 RMVar_ID_89021 Human_SNP_ID_482525525 m1A Human chr11 - 114312239 114312239 114312239 CCATGATCACCAGGAAGCCCCCTGGCTTCAGTAGGCTGCCGAGGTTCCTGAGCGCCCTGCAGTAG CCATGATCACCAGGAAGCCCCCTGGCTTCAGTTGGCTGCCGAGGTTCCTGAGCGCCCTGCAGTAG T A AP002518.2 Ensembl:ENSG00000256947 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:114312026..114312250 32194978 MeRIP-seq:(Medium) rs142397660 Functional Loss SNV dbSNP153 33..33 33 - - - 89022 RMVar_ID_89022 Human_SNP_ID_482525526 m1A Human chr11 - 114312239 114312239 114312239 CCATGATCACCAGGAAGCCCCCTGGCTTCAGTAGGCTGCCGAGGTTCCTGAGCGCCCTGCAGTAG CCATGATCACCAGGAAGCCCCCTGGCTTCAGTGGGCTGCCGAGGTTCCTGAGCGCCCTGCAGTAG T C AP002518.2 Ensembl:ENSG00000256947 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:114312026..114312250 32194978 MeRIP-seq:(Medium) rs142397660 Functional Loss SNV dbSNP153 33..33 33 - - - 89023 RMVar_ID_89023 Human_SNP_ID_482525616 m1A Human chr11 + 114312407 114312407 114312407 AATCGAATGGTTTGAGGTGATCTCGCAAAGTTATTCTTCCACCATGGCCAACAACGAAGGACTTT AATCGAATGGTTTGAGGTGATCTCGCAAAGTTGTTCTTCCACCATGGCCAACAACGAAGGACTTT A G NNMT Ensembl:ENSG00000166741 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:114312357..114312429 26863196 MeRIP-seq:(Medium) rs771908773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31265 Human_miRNA_ID_2393258 RMVar_hsa_circ_118280,RMVar_hsa_circ_80088,RMVar_hsa_circ_110154,RMVar_hsa_circ_153179,RMVar_hsa_circ_153180,RMVar_hsa_circ_94002,RMVar_hsa_circ_118596,RMVar_hsa_circ_153181,RMVar_hsa_circ_121980,RMVar_hsa_circ_153182,RMVar_hsa_circ_153183,RMVar_hsa_circ_153184 89024 RMVar_ID_89024 Human_SNP_ID_482546860 m1A Human chr11 - 114400101 114400097 114400102 CGAGTGGATGGTGGCGGCCGGAGCCCAAGGGAACCAGATGGCCGGGGCCGGAGCCGCCAAGCCAG CGAGTGGATGGTGGCGGCCGGAGCCCAAGGG_____GATGGCCGGGGCCGGAGCCGCCAAGCCAG CTGGTT C C11orf71 Ensembl:ENSG00000180425 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:114400052..114400135 26863196 MeRIP-seq:(Medium) rs746417834 Functional Loss DEL dbSNP153 32..36 33 - - - 89025 RMVar_ID_89025 Human_SNP_ID_482546865 m1A Human chr11 - 114400101 114400101 114400101 CGAGTGGATGGTGGCGGCCGGAGCCCAAGGGAACCAGATGGCCGGGGCCGGAGCCGCCAAGCCAG CGAGTGGATGGTGGCGGCCGGAGCCCAAGGGAGCCAGATGGCCGGGGCCGGAGCCGCCAAGCCAG T C C11orf71 Ensembl:ENSG00000180425 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:114400052..114400135 26863196 MeRIP-seq:(Medium) rs761859666 Functional Loss SNV dbSNP153 33..33 33 - - - 89026 RMVar_ID_89026 Human_SNP_ID_482547047 m1A Human chr11 - 114400485 114400485 114400485 CTGCGCATGCTCGCCAGGATACCCCTCGTTAAAGGCAAGGCGGCTTCTGGCTCTTCCGCAGGCTC CTGCGCATGCTCGCCAGGATACCCCTCGTTAAGGGCAAGGCGGCTTCTGGCTCTTCCGCAGGCTC T C C11orf71 Ensembl:ENSG00000180425 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs606671 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11568,GWAS_ID_11569,GWAS_ID_11570 89027 RMVar_ID_89027 Human_SNP_ID_482547193 m1A Human chr11 + 114400730 114400730 114400730 TCGCACTCTCTTTGTGGGCAACCTTGAAACGAAAGTGACCGAGGAGCTCCTTTTCGAGCTTTTCC TCGCACTCTCTTTGTGGGCAACCTTGAAACGACAGTGACCGAGGAGCTCCTTTTCGAGCTTTTCC A C AP002373.1,RBM7 Ensembl:ENSG00000255663,Ensembl:ENSG00000076053 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:114400592..114400754 26863196 MeRIP-seq:(Medium) rs958509263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185387,Human_RBP_ID_9322346,Human_RBP_ID_11527240 Human_Splice_Rec_1300113,Human_Splice_Rec_1300121,Human_Splice_Rec_1300129,Human_Splice_Rec_1300135,Human_Splice_Rec_1300141,Human_Splice_Rec_1300147,Human_Splice_Rec_1300155,Human_Splice_Rec_1300163,Human_Splice_Rec_1300167,Human_Splice_Rec_1300169 89028 RMVar_ID_89028 Human_SNP_ID_483142345 m1A Human chr11 - 116759154 116759154 116759154 TGCATAGGCTGCACACATGTATTCTGGGGCTAAAACTGGGTTGGTGTTAACTGACATACAGCGAG TGCATAGGCTGCACACATGTATTCTGGGGCTATAACTGGGTTGGTGTTAACTGACATACAGCGAG T A BUD13 Ensembl:ENSG00000137656 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:116759109..116760815 32194978 MeRIP-seq:(Medium) rs1308085706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8766868,Human_RBP_ID_18603379 Human_Splice_Rec_1300768,Human_Splice_Rec_1300769,Human_Splice_Rec_1300786,Human_Splice_Rec_1300787 RMVar_hsa_circ_98925,RMVar_hsa_circ_106614,RMVar_hsa_circ_153212,RMVar_hsa_circ_98419,RMVar_hsa_circ_153213,RMVar_hsa_circ_356270,RMVar_hsa_circ_153211,RMVar_hsa_circ_347007,RMVar_hsa_circ_279087,RMVar_hsa_circ_39426,RMVar_hsa_circ_153215,RMVar_hsa_circ_282494 89029 RMVar_ID_89029 Human_SNP_ID_483143456 m1A Human chr11 - 116763161 116763161 116763161 TCATGGTACCCCAGATCCATCTCCTAGGAAGGACCGTCATGACACCCCGGATCCATCTCCTAGGA TCATGGTACCCCAGATCCATCTCCTAGGAAGGTCCGTCATGACACCCCGGATCCATCTCCTAGGA T A BUD13 Ensembl:ENSG00000137656 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:116763112..116765408 32194978 MeRIP-seq:(Medium) rs1405389757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8766870,Human_RBP_ID_26805161,Human_RBP_ID_27408941 RMVar_hsa_circ_106614,RMVar_hsa_circ_153212,RMVar_hsa_circ_98419,RMVar_hsa_circ_356270,RMVar_hsa_circ_153211,RMVar_hsa_circ_279087,RMVar_hsa_circ_39426,RMVar_hsa_circ_153215,RMVar_hsa_circ_282494,RMVar_hsa_circ_371116,RMVar_hsa_circ_326875,RMVar_hsa_circ_153216,RMVar_hsa_circ_153217 89030 RMVar_ID_89030 Human_SNP_ID_483143457 m1A Human chr11 - 116763161 116763161 116763161 TCATGGTACCCCAGATCCATCTCCTAGGAAGGACCGTCATGACACCCCGGATCCATCTCCTAGGA TCATGGTACCCCAGATCCATCTCCTAGGAAGGCCCGTCATGACACCCCGGATCCATCTCCTAGGA T G BUD13 Ensembl:ENSG00000137656 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:116763112..116765408 32194978 MeRIP-seq:(Medium) rs1405389757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8766870,Human_RBP_ID_26805161,Human_RBP_ID_27408941 RMVar_hsa_circ_106614,RMVar_hsa_circ_153212,RMVar_hsa_circ_98419,RMVar_hsa_circ_356270,RMVar_hsa_circ_153211,RMVar_hsa_circ_279087,RMVar_hsa_circ_39426,RMVar_hsa_circ_153215,RMVar_hsa_circ_282494,RMVar_hsa_circ_371116,RMVar_hsa_circ_326875,RMVar_hsa_circ_153216,RMVar_hsa_circ_153217 89031 RMVar_ID_89031 Human_SNP_ID_483148330 m1A Human chr11 - 116782238 116782238 116782238 ATAGTTTGGATTATCATTTATTGCAGGTGACCAAAAATCCTTTCACACTGGGCGACAGTTCCAAT ATAGTTTGGATTATCATTTATTGCAGGTGACCGAAAATCCTTTCACACTGGGCGACAGTTCCAAT T C ZPR1 Ensembl:ENSG00000109917 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:116779786..116786572 32194978 MeRIP-seq:(Medium) rs373537056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1353621,Human_RBP_ID_9362939,Human_RBP_ID_17790379 Human_Splice_Rec_1300818,Human_Splice_Rec_1300819,Human_Splice_Rec_1300842,Human_Splice_Rec_1300843,Human_Splice_Rec_1300884 RMVar_hsa_circ_83647,RMVar_hsa_circ_123756,RMVar_hsa_circ_110124,RMVar_hsa_circ_93828,RMVar_hsa_circ_153219,RMVar_hsa_circ_153221,RMVar_hsa_circ_78537,RMVar_hsa_circ_153222,RMVar_hsa_circ_153220,RMVar_hsa_circ_63879,RMVar_hsa_circ_153218,RMVar_hsa_circ_365265 89032 RMVar_ID_89032 Human_SNP_ID_483149723 m1A Human chr11 - 116787852 116787852 116787852 GCGCCGAGGACGAGGAGCAGCAGCCCACCGAGATCGAGTCGCTATGCATGAACTGTTACTGCAAT GCGCCGAGGACGAGGAGCAGCAGCCCACCGAGGTCGAGTCGCTATGCATGAACTGTTACTGCAAT T C ZPR1 Ensembl:ENSG00000109917 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:116787850..116787950 32194978 MeRIP-seq:(Medium) rs1362125510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4148508,Human_RBP_ID_9364296,Human_RBP_ID_23488118,Human_RBP_ID_26885917 Human_Splice_Rec_1300797,Human_Splice_Rec_1300825,Human_Splice_Rec_1300847,Human_Splice_Rec_1300885,Human_Splice_Rec_1300895 RMVar_hsa_circ_89593,RMVar_hsa_circ_153226 89033 RMVar_ID_89033 Human_SNP_ID_483149754 m1A Human chr11 + 116787907 116787906 116787907 TCCTCGGCGCTGATGGGCCGGAACAGGTGATCAGGGGCAGGCGGCGGGGCCGGGGCGGGCGACGG TCCTCGGCGCTGATGGGCCGGAACAGGTGATC_GGGGCAGGCGGCGGGGCCGGGGCGGGCGACGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:116787860..116788000 26863196 MeRIP-seq:(Medium) rs1034968307 Functional Loss DEL dbSNP153 33..33 33 - - - 89034 RMVar_ID_89034 Human_SNP_ID_483149755 m1A Human chr11 + 116787907 116787907 116787907 TCCTCGGCGCTGATGGGCCGGAACAGGTGATCAGGGGCAGGCGGCGGGGCCGGGGCGGGCGACGG TCCTCGGCGCTGATGGGCCGGAACAGGTGATCGGGGGCAGGCGGCGGGGCCGGGGCGGGCGACGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:116787860..116788000 26863196 MeRIP-seq:(Medium) rs759598502 Functional Loss SNV dbSNP153 33..33 33 - - - 89035 RMVar_ID_89035 Human_SNP_ID_483149790 m1A Human chr11 + 116787944 116787944 116787944 CAGGCGGCGGGGCCGGGGCGGGCGACGGGGCGACGGCAGCCCCCGGGGGCCCTGGTTCCACAGCC CAGGCGGCGGGGCCGGGGCGGGCGACGGGGCGGCGGCAGCCCCCGGGGGCCCTGGTTCCACAGCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:116787826..116788025 26863410 MeRIP-seq:(Medium) rs1255954256 Functional Loss SNV dbSNP153 33..33 33 - - - 89036 RMVar_ID_89036 Human_SNP_ID_483184247 m1A Human chr11 + 116920115 116920115 116920115 TATAAACATCTACTGCTCCTGCCTTCTCGGGGAGACTCCTCTCCTTTAGCCTTCCCTTCCACTGA TATAAACATCTACTGCTCCTGCCTTCTCGGGGGGACTCCTCTCCTTTAGCCTTCCCTTCCACTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:116920107..116920345 26863196 MeRIP-seq:(Medium) rs1335352689 Functional Loss SNV dbSNP153 33..33 33 - - - 89037 RMVar_ID_89037 Human_SNP_ID_483228406 m1A Human chr11 - 117098263 117098263 117098263 GTGTCCCCTGCGGCCGGCCAGCCGCGTCCCCCAGCCCCGGCCTCCCGCGGACCCATGCCCGCCCG GTGTCCCCTGCGGCCGGCCAGCCGCGTCCCCCTGCCCCGGCCTCCCGCGGACCCATGCCCGCCCG T A SIK3 Ensembl:ENSG00000160584 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117098212..117098395 26863196 MeRIP-seq:(Medium) rs978531524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9362946,Human_RBP_ID_18417029,Human_RBP_ID_26775712,Human_RBP_ID_27804038 Human_miRNA_ID_1034738,Human_miRNA_ID_2684814 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 89038 RMVar_ID_89038 Human_SNP_ID_483228415 m1A Human chr11 - 117098276 117098276 117098276 CGCCCCCGCTGCCGTGTCCCCTGCGGCCGGCCAGCCGCGTCCCCCAGCCCCGGCCTCCCGCGGAC CGCCCCCGCTGCCGTGTCCCCTGCGGCCGGCCCGCCGCGTCCCCCAGCCCCGGCCTCCCGCGGAC T G SIK3 Ensembl:ENSG00000160584 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117097644..117098384 26863196 MeRIP-seq:(Medium) rs1442420484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4148543,Human_RBP_ID_9364305,Human_RBP_ID_18417029,Human_RBP_ID_26775712,Human_RBP_ID_27804038 Human_miRNA_ID_2684814 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 89039 RMVar_ID_89039 Human_SNP_ID_483228451 m1A Human chr11 + 117098365 117098365 117098365 GGCAGCAGGCGGCCCGCGGGCCCGGCTCCCCCAGTCCCGGCCCCGGCAGCCCCGCCAGCTCCGCT GGCAGCAGGCGGCCCGCGGGCCCGGCTCCCCCCGTCCCGGCCCCGGCAGCCCCGCCAGCTCCGCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:116957009..117098396 26863196 MeRIP-seq:(Medium) rs1359988623 Functional Loss SNV dbSNP153 33..33 33 - - - 89040 RMVar_ID_89040 Human_SNP_ID_483228452 m1A Human chr11 + 117098365 117098365 117098365 GGCAGCAGGCGGCCCGCGGGCCCGGCTCCCCCAGTCCCGGCCCCGGCAGCCCCGCCAGCTCCGCT GGCAGCAGGCGGCCCGCGGGCCCGGCTCCCCCGGTCCCGGCCCCGGCAGCCCCGCCAGCTCCGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:116957009..117098396 26863196 MeRIP-seq:(Medium) rs1359988623 Functional Loss SNV dbSNP153 33..33 33 - - - 89041 RMVar_ID_89041 Human_SNP_ID_483238838 m1A Human chr11 + 117138591 117138591 117138591 GCACGGGAAGGAGGAGCAGATCTGCTGACCTCAGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC GCACGGGAAGGAGGAGCAGATCTGCTGACCTCGGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs560621 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - 89042 RMVar_ID_89042 Human_SNP_ID_483240468 m1A Human chr11 + 117144370 117144370 117144370 ACCGACGGGACCGAGCGAGCGACCGACGCGCCACCCGCCGACGCCTCAGCCGCTTGGGGCCCGCA ACCGACGGGACCGAGCGAGCGACCGACGCGCCCCCCGCCGACGCCTCAGCCGCTTGGGGCCCGCA A C PAFAH1B2 Ensembl:ENSG00000168092 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:117144322..117144465;chr11:117144326..117144469 26863196 MeRIP-seq:(Medium) rs955151039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226987,Human_RBP_ID_4184430,Human_RBP_ID_5314461,Human_RBP_ID_19050471 Human_Splice_Rec_1301275,Human_Splice_Rec_1301283,Human_Splice_Rec_1301293,Human_Splice_Rec_1301297,Human_Splice_Rec_1301307,Human_Splice_Rec_1301309,Human_Splice_Rec_1301321 RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_153255 89043 RMVar_ID_89043 Human_SNP_ID_483251105 m1A Human chr11 + 117178832 117178832 117178832 AAACTCGCAGCCCAGCACGGCGTCGGGTAGCTACCACCTATCACGCCCCTCACTCTGCGACTCGC AAACTCGCAGCCCAGCACGGCGTCGGGTAGCTTCCACCTATCACGCCCCTCACTCTGCGACTCGC A T SIDT2 Ensembl:ENSG00000149577 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:117178782..117179032 26863196 MeRIP-seq:(Medium) rs1001550638 Functional Loss SNV dbSNP153 33..33 33 - - - 89044 RMVar_ID_89044 Human_SNP_ID_483251111 m1A Human chr11 + 117178842 117178842 117178842 CCCAGCACGGCGTCGGGTAGCTACCACCTATCACGCCCCTCACTCTGCGACTCGCCTTCCTCCGC CCCAGCACGGCGTCGGGTAGCTACCACCTATCGCGCCCCTCACTCTGCGACTCGCCTTCCTCCGC A G SIDT2 Ensembl:ENSG00000149577 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117178796..117178941 26863196 MeRIP-seq:(Medium) rs1374400075 Functional Loss SNV dbSNP153 33..33 33 - - - 89045 RMVar_ID_89045 Human_SNP_ID_483251265 m1A Human chr11 - 117179215 117179215 117179215 CAGTGGCAGCGGTGGTGGCGGCGGCGGCGGCGACAGGAGACAGGACACCTCCGGGACGGGTTGCG CAGTGGCAGCGGTGGTGGCGGCGGCGGCGGCGGCAGGAGACAGGACACCTCCGGGACGGGTTGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117179168..117179299 26863196 MeRIP-seq:(Medium) rs1311508915 Functional Loss SNV dbSNP153 33..33 33 - - - 89046 RMVar_ID_89046 Human_SNP_ID_483256567 m1A Human chr11 + 117196445 117196445 117196445 ATGCCTTGCATTTTGCCCGTCCTCCTCCCCACAATGCCCCAGCCTGGGACCTAAGGCCTCTTTTT ATGCCTTGCATTTTGCCCGTCCTCCTCCCCACCATGCCCCAGCCTGGGACCTAAGGCCTCTTTTT A C SIDT2 Ensembl:ENSG00000149577 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:117196399..117196649 32194978 MeRIP-seq:(Medium) rs889929900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17074047 Human_miRNA_ID_841795,Human_miRNA_ID_1417665,Human_miRNA_ID_2684815,Human_miRNA_ID_2725855 RMVar_hsa_circ_266347,RMVar_hsa_circ_115264,RMVar_hsa_circ_153280 89047 RMVar_ID_89047 Human_SNP_ID_483258308 m1A Human chr11 + 117203041 117203041 117203041 CAGACATGGCCAACAAGGGTCCTTCCTATGGCATGAGCCGCGAAGTGCAGTCCAAAATCGAGAAG CAGACATGGCCAACAAGGGTCCTTCCTATGGCGTGAGCCGCGAAGTGCAGTCCAAAATCGAGAAG A G TAGLN Ensembl:ENSG00000149591 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117203001..117203150 26863196 MeRIP-seq:(Medium) rs1461342630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18432371 Human_Splice_Rec_1301708,Human_Splice_Rec_1301718,Human_Splice_Rec_1301726,Human_Splice_Rec_1301734,Human_Splice_Rec_1301740 89048 RMVar_ID_89048 Human_SNP_ID_483258330 m1A Human chr11 + 117203084 117203082 117203085 AGTGCAGTCCAAAATCGAGAAGAAGTATGACGAGGAGCTGGAGGAGCGGCTGGTGGAGTGGATCA AGTGCAGTCCAAAATCGAGAAGAAGTATGAC___GAGCTGGAGGAGCGGCTGGTGGAGTGGATCA CGAG C TAGLN Ensembl:ENSG00000149591 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117203036..117203137 26863196 MeRIP-seq:(Medium) rs778782959 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22571914 Human_Splice_Rec_1301708,Human_Splice_Rec_1301718,Human_Splice_Rec_1301726,Human_Splice_Rec_1301734,Human_Splice_Rec_1301740,Human_Splice_Rec_1301753 89049 RMVar_ID_89049 Human_SNP_ID_483258348 m1A Human chr11 - 117203114 117203114 117203114 GGCGGCCCACATCAGGGCCACACTGCACTATGATCCACTCCACCAGCCGCTCCTCCAGCTCCTCG GGCGGCCCACATCAGGGCCACACTGCACTATGTTCCACTCCACCAGCCGCTCCTCCAGCTCCTCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117202947..117203321 26863196 MeRIP-seq:(Medium) rs1390567639 Functional Loss SNV dbSNP153 33..33 33 - - - 89050 RMVar_ID_89050 Human_SNP_ID_483258368 m1A Human chr11 + 117203171 117203171 117203171 GGGCCGCCCAGACCGTGGGCGCTTGGGCTTCCAGGTCTGGCTGAAGAATGGCGTGGTGAGTGGCA GGGCCGCCCAGACCGTGGGCGCTTGGGCTTCCGGGTCTGGCTGAAGAATGGCGTGGTGAGTGGCA A G TAGLN Ensembl:ENSG00000149591 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:117202997..117203196;chr11:117203001..117203200 32194978 MeRIP-seq:(Medium) rs1377358166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1301709,Human_Splice_Rec_1301719,Human_Splice_Rec_1301727,Human_Splice_Rec_1301735,Human_Splice_Rec_1301741,Human_Splice_Rec_1301747,Human_Splice_Rec_1301753 89051 RMVar_ID_89051 Human_SNP_ID_483258495 m1A Human chr11 - 117203486 117203486 117203486 TGCCCACCTCCTCCCCCAGCCTCTTCCTCTCTACCTTCAAAGAGGTCAACAGTCTGGAACATGTC TGCCCACCTCCTCCCCCAGCCTCTTCCTCTCTGCCTTCAAAGAGGTCAACAGTCTGGAACATGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:117203476..117203500 32194978 MeRIP-seq:(Medium) rs112388114 Functional Loss SNV dbSNP153 33..33 33 - - - 89052 RMVar_ID_89052 Human_SNP_ID_483258841 m1A Human chr11 - 117204390 117204390 117204390 AAGCGGGATGGCTGCAGCCAAGGAGCTGGGGGAGGGCCGGGCTCAGGGCTAGCCCTCTCCGCTCT AAGCGGGATGGCTGCAGCCAAGGAGCTGGGGGCGGGCCGGGCTCAGGGCTAGCCCTCTCCGCTCT T G PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:117204201..117204750 32194978 MeRIP-seq:(Medium) rs539235979 Functional Loss SNV dbSNP153 33..33 33 - - - 89053 RMVar_ID_89053 Human_SNP_ID_483258909 m1A Human chr11 - 117204569 117204569 117204569 GAGGTGATGGGGGCAGCCGGGAGGGAGGGGCCAAGGCAGTGATGCTTTCGGGTAAGAAGTTGGGC GAGGTGATGGGGGCAGCCGGGAGGGAGGGGCCGAGGCAGTGATGCTTTCGGGTAAGAAGTTGGGC T C PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117204194..117204690 26863196 MeRIP-seq:(Medium) rs757670102 Functional Loss SNV dbSNP153 33..33 33 - - - 89054 RMVar_ID_89054 Human_SNP_ID_483258936 m1A Human chr11 - 117204658 117204658 117204658 TTTGCCGCCAAGGAGGACAGTGGACTTGGCCCACATCCAGGCTACCCCCAGCCCGCTTCTCCCCT TTTGCCGCCAAGGAGGACAGTGGACTTGGCCCCCATCCAGGCTACCCCCAGCCCGCTTCTCCCCT T G PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:117204201..117204750 32194978 MeRIP-seq:(Medium) rs1379288155 Functional Loss SNV dbSNP153 33..33 33 - - - 89055 RMVar_ID_89055 Human_SNP_ID_483259306 m1A Human chr11 - 117205992 117205990 117205992 GCACGGGAAGGAGGAGCAGATCTGCTGACCTCAGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC GCACGGGAAGGAGGAGCAGATCTGCTGACCTC__GGCCTGACAGTGTGGGACAGGCTCTTCTTTC CCT C PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1261327966 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_82321,RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153290,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286 89056 RMVar_ID_89056 Human_SNP_ID_483259308 m1A Human chr11 - 117205992 117205992 117205992 GCACGGGAAGGAGGAGCAGATCTGCTGACCTCAGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC GCACGGGAAGGAGGAGCAGATCTGCTGACCTCGGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC T C PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35186251 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_82321,RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153290,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286 89057 RMVar_ID_89057 Human_SNP_ID_483264657 m1A Human chr11 + 117224869 117224869 117224869 TGCCCTTTGACCTGCAGCTCTTAACTCCTCCCAAGGGTTCCACTTAAAGGCTTCCGTGATTAAAA TGCCCTTTGACCTGCAGCTCTTAACTCCTCCCCAGGGTTCCACTTAAAGGCTTCCGTGATTAAAA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:117224742..117224871 26863196 MeRIP-seq:(Medium) rs1565315894 Functional Loss SNV dbSNP153 33..33 33 - - - 89058 RMVar_ID_89058 Human_SNP_ID_483265655 m1A Human chr11 - 117228300 117228300 117228300 GGCAGGGACATCAACGTGACGGGTGTGTGGGAACGCAATGTGACTGGGCGAGGGGTGACGGTGGT GGCAGGGACATCAACGTGACGGGTGTGTGGGAGCGCAATGTGACTGGGCGAGGGGTGACGGTGGT T C PCSK7 Ensembl:ENSG00000160613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117228251..117228391 26863196 MeRIP-seq:(Medium) rs1251137850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226793,Human_RBP_ID_3941255,Human_RBP_ID_18972781,Human_RBP_ID_26319240 Human_Splice_Rec_1301764,Human_Splice_Rec_1301765,Human_Splice_Rec_1301816,Human_Splice_Rec_1301817,Human_Splice_Rec_1301878,Human_Splice_Rec_1301879 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294,RMVar_hsa_circ_268971 89059 RMVar_ID_89059 Human_SNP_ID_483266007 m1A Human chr11 - 117229474 117229474 117229474 CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCATGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCTTGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC T A PCSK7 Ensembl:ENSG00000160613 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117229423..117229868 26863196 MeRIP-seq:(Medium) rs985732997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871184,Human_RBP_ID_6048039 Human_Splice_Rec_1301763,Human_Splice_Rec_1301815,Human_Splice_Rec_1301877 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294,RMVar_hsa_circ_267555 89060 RMVar_ID_89060 Human_SNP_ID_483266008 m1A Human chr11 - 117229474 117229474 117229474 CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCATGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCGTGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC T C PCSK7 Ensembl:ENSG00000160613 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117229423..117229868 26863196 MeRIP-seq:(Medium) rs985732997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871184,Human_RBP_ID_6048039 Human_Splice_Rec_1301763,Human_Splice_Rec_1301815,Human_Splice_Rec_1301877 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294,RMVar_hsa_circ_267555 89061 RMVar_ID_89061 Human_SNP_ID_483266288 m1A Human chr11 - 117230329 117230329 117230329 ATGTAGAATCCAGGTGGGCACGGGGCCCTGTTATGGGGAATTAGCCTTGAGGACAACTGGACTGA ATGTAGAATCCAGGTGGGCACGGGGCCCTGTTTTGGGGAATTAGCCTTGAGGACAACTGGACTGA T A PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117230325..117230419 26863196 MeRIP-seq:(Medium) rs1030900934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865531,Human_RBP_ID_19053125 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294 89062 RMVar_ID_89062 Human_SNP_ID_483280085 m1A Human chr11 - 117279853 117279853 117279853 CAAGACTAAGGAAGAAAGATAAGCTTGTTGAGAGATACCAGGGCAAAAGTACAACCCAAAATTGG CAAGACTAAGGAAGAAAGATAAGCTTGTTGAGCGATACCAGGGCAAAAGTACAACCCAAAATTGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117279848..117279940 26863196 MeRIP-seq:(Medium) rs1158136246 Functional Loss SNV dbSNP153 33..33 33 - - - 89063 RMVar_ID_89063 Human_SNP_ID_483281990 m1A Human chr11 - 117287353 117287353 117287353 TCTGCTCCTGAAAAATGACTGTCCCATTCTCCACTCACTGCATTTGGGGCCTTTCCCATTGGTCT TCTGCTCCTGAAAAATGACTGTCCCATTCTCCGCTCACTGCATTTGGGGCCTTTCCCATTGGTCT T C BACE1 Ensembl:ENSG00000186318 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:117287303..117287404 32194978 MeRIP-seq:(Medium) rs991674373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_133589 89064 RMVar_ID_89064 Human_SNP_ID_483285200 m1A Human chr11 - 117299405 117299405 117299405 TCTGGCAGAGAGGACGAAACTGAAGTCCAGAGAAGCACAGTGATCTGCTCAAGGTGACAGGGTCA TCTGGCAGAGAGGACGAAACTGAAGTCCAGAGCAGCACAGTGATCTGCTCAAGGTGACAGGGTCA T G BACE1 Ensembl:ENSG00000186318 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117299402..117299653 26863196 MeRIP-seq:(Medium) rs964499826 Functional Loss SNV dbSNP153 33..33 33 - - - 89065 RMVar_ID_89065 Human_SNP_ID_483285436 m1A Human chr11 + 117300264 117300264 117300264 CAGGTCCCCACTGCTCTCTGCCTCCCCTCTCCACCTTACACACACACACAAAAGAAAACCAGAAT CAGGTCCCCACTGCTCTCTGCCTCCCCTCTCCGCCTTACACACACACACAAAAGAAAACCAGAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117300260..117300379 26863196 MeRIP-seq:(Medium) rs1266262820 Functional Loss SNV dbSNP153 33..33 33 - - - 89066 RMVar_ID_89066 Human_SNP_ID_483289209 m1A Human chr11 + 117315605 117315605 117315605 AGCCCTGCCCCGACTTGCCCCTCAGGTTGTCCACCATCTCCACAAAGCTGCCCCTCCGGCCGGGC AGCCCTGCCCCGACTTGCCCCTCAGGTTGTCCGCCATCTCCACAAAGCTGCCCCTCCGGCCGGGC A G CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117315517..117315795 26863196 MeRIP-seq:(Medium) rs764642283 Functional Loss SNV dbSNP153 33..33 33 - - - 89067 RMVar_ID_89067 Human_SNP_ID_483289235 m1A Human chr11 + 117315680 117315680 117315680 CTTCGTCGGTCTCCCGGGGCAGCCGCAGCCCCAGGGGGGCGCCCCCCAGGCCGCTGCGCAGGGGC CTTCGTCGGTCTCCCGGGGCAGCCGCAGCCCCTGGGGGGCGCCCCCCAGGCCGCTGCGCAGGGGC A T CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117315631..117315715 26863196 MeRIP-seq:(Medium) rs1006804785 Functional Loss SNV dbSNP153 33..33 33 - - - 89068 RMVar_ID_89068 Human_SNP_ID_483289370 m1A Human chr11 - 117316124 117316124 117316124 TGCCCCTGCCCGCGCCGCCGCCCGCCGGGGGGACCAGGGAAGCCGCCACCGGCCCGCCATGCCCG TGCCCCTGCCCGCGCCGCCGCCCGCCGGGGGGGCCAGGGAAGCCGCCACCGGCCCGCCATGCCCG T C BACE1 Ensembl:ENSG00000186318 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:117316041..117316250 26863410 MeRIP-seq:(Medium) rs1220982960 Functional Loss SNV dbSNP153 33..33 33 - - - 89069 RMVar_ID_89069 Human_SNP_ID_483289408 m1A Human chr11 - 117316217 117316217 117316217 TTTCCGCCTCCCCAGCCCGCCCGGGAGCTGCGAGCCGCGAGCTGGATTATGGTGGCCTGAGCAGC TTTCCGCCTCCCCAGCCCGCCCGGGAGCTGCGCGCCGCGAGCTGGATTATGGTGGCCTGAGCAGC T G BACE1 Ensembl:ENSG00000186318 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:117315976..117316275 26863196 MeRIP-seq:(Medium) rs1287411624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_389678 89070 RMVar_ID_89070 Human_SNP_ID_483307176 m1A Human chr11 - 117389721 117389721 117389721 TACCACACTCTTCCTTCCTAGGTTCTCTGCCAAGAATTCCCTTTTCTATCTGGCAAACCCATATT TACCACACTCTTCCTTCCTAGGTTCTCTGCCACGAATTCCCTTTTCTATCTGGCAAACCCATATT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117389712..117389777 26863196 MeRIP-seq:(Medium) rs1006198749 Functional Loss SNV dbSNP153 33..33 33 - - - 89071 RMVar_ID_89071 Human_SNP_ID_483307452 m1A Human chr11 + 117390826 117390826 117390826 TGCAGAAAGCCATTGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGAAAGCCAGAGGCTATCCTGG TGCAGAAAGCCATTGAGGAGGAGGAGGCCCGGGTGAGAGAGGAGGAAAGCCAGAGGCTATCCTGG A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117390769..117390884 26863196 MeRIP-seq:(Medium) rs142710882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226374,Human_RBP_ID_26319253 Human_Splice_Rec_1302232,Human_Splice_Rec_1302233,Human_Splice_Rec_1302314,Human_Splice_Rec_1302315,Human_Splice_Rec_1302362,Human_Splice_Rec_1302363,Human_Splice_Rec_1302402,Human_Splice_Rec_1302403,Human_Splice_Rec_1302406,Human_Splice_Rec_1302407 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_329540,RMVar_hsa_circ_153321 89072 RMVar_ID_89072 Human_SNP_ID_483307453 m1A Human chr11 + 117390833 117390831 117390834 AGCCATTGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAG AGCCATTGAGGAGGAGGAGGCCCGGATGAGA___GAGGAAAGCCAGAGGCTATCCTGGCTCCGAG AGAG A CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117390784..117390889 26863196 MeRIP-seq:(Medium) rs1444193382 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_226374,Human_RBP_ID_26319253 Human_Splice_Rec_1302232,Human_Splice_Rec_1302233,Human_Splice_Rec_1302314,Human_Splice_Rec_1302315,Human_Splice_Rec_1302362,Human_Splice_Rec_1302363,Human_Splice_Rec_1302402,Human_Splice_Rec_1302403,Human_Splice_Rec_1302406,Human_Splice_Rec_1302407 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_329540,RMVar_hsa_circ_153321 89073 RMVar_ID_89073 Human_SNP_ID_483307455 m1A Human chr11 + 117390833 117390833 117390833 AGCCATTGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAG AGCCATTGAGGAGGAGGAGGCCCGGATGAGAGCGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAG A C CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117390784..117390889 26863196 MeRIP-seq:(Medium) rs150261648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226374,Human_RBP_ID_26319253 Human_Splice_Rec_1302232,Human_Splice_Rec_1302233,Human_Splice_Rec_1302314,Human_Splice_Rec_1302315,Human_Splice_Rec_1302362,Human_Splice_Rec_1302363,Human_Splice_Rec_1302402,Human_Splice_Rec_1302403,Human_Splice_Rec_1302406,Human_Splice_Rec_1302407 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_329540,RMVar_hsa_circ_153321 89074 RMVar_ID_89074 Human_SNP_ID_483307458 m1A Human chr11 + 117390839 117390839 117390839 TGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAGCTCAGG TGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGGAAGCCAGAGGCTATCCTGGCTCCGAGCTCAGG A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117390755..117391162 26863196 MeRIP-seq:(Medium) rs1473205938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226374,Human_RBP_ID_26319253 Human_Splice_Rec_1302232,Human_Splice_Rec_1302233,Human_Splice_Rec_1302314,Human_Splice_Rec_1302315,Human_Splice_Rec_1302362,Human_Splice_Rec_1302363,Human_Splice_Rec_1302402,Human_Splice_Rec_1302403,Human_Splice_Rec_1302406,Human_Splice_Rec_1302407 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_329540,RMVar_hsa_circ_153321 89075 RMVar_ID_89075 Human_SNP_ID_483308017 m1A Human chr11 + 117392626 117392626 117392626 GAAGTCTTATCACGTGGCTGGGTATGAGCACGAGGTGAGTGCTGCTCTGTCTTCCACAGTCGTGT GAAGTCTTATCACGTGGCTGGGTATGAGCACGGGGTGAGTGCTGCTCTGTCTTCCACAGTCGTGT A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117392483..117392671 26863196 MeRIP-seq:(Medium) rs770584842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520974 Human_Splice_Rec_1302239,Human_Splice_Rec_1302321,Human_Splice_Rec_1302369,Human_Splice_Rec_1302413 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_88362,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_153322,RMVar_hsa_circ_98540,RMVar_hsa_circ_153323 89076 RMVar_ID_89076 Human_SNP_ID_483308182 m1A Human chr11 + 117393089 117393089 117393089 GAGGTTGGACAAGATGAAGGAGGAGCACCAGCAAGTGATGGCTAAGGCCAGAGAGCAGTATGAAG GAGGTTGGACAAGATGAAGGAGGAGCACCAGCGAGTGATGGCTAAGGCCAGAGAGCAGTATGAAG A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117392983..117393166 26863196 MeRIP-seq:(Medium) rs1041526136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868395,Human_RBP_ID_18974975,Human_RBP_ID_27805116 Human_Splice_Rec_1302240,Human_Splice_Rec_1302241,Human_Splice_Rec_1302322,Human_Splice_Rec_1302323,Human_Splice_Rec_1302370,Human_Splice_Rec_1302371,Human_Splice_Rec_1302414,Human_Splice_Rec_1302415 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_88362,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_153322,RMVar_hsa_circ_98540,RMVar_hsa_circ_153323 89077 RMVar_ID_89077 Human_SNP_ID_483308195 m1A Human chr11 - 117393115 117393115 117393115 CAGGGGATGTGGCTGAGCTACCTCAGCTTCATACTGCTCTCTGGCCTTAGCCATCACTTGCTGGT CAGGGGATGTGGCTGAGCTACCTCAGCTTCATGCTGCTCTCTGGCCTTAGCCATCACTTGCTGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:117393064..117393164 26863196 MeRIP-seq:(Medium) rs774896440 Functional Loss SNV dbSNP153 33..33 33 - - - 89078 RMVar_ID_89078 Human_SNP_ID_483308558 m1A Human chr11 + 117394410 117394410 117394410 GGCACCTGACCGGAGAGCTGGAGCGCCTGCAGAGGGCCCATGAACGAGAACTGGAGACTGTGAGG GGCACCTGACCGGAGAGCTGGAGCGCCTGCAGGGGGCCCATGAACGAGAACTGGAGACTGTGAGG A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117394283..117394481 26863196 MeRIP-seq:(Medium) rs1316877137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226375,Human_RBP_ID_5520976,Human_RBP_ID_5548925,Human_RBP_ID_18974976 Human_Splice_Rec_1302242,Human_Splice_Rec_1302243,Human_Splice_Rec_1302324,Human_Splice_Rec_1302325,Human_Splice_Rec_1302372,Human_Splice_Rec_1302373,Human_Splice_Rec_1302416,Human_Splice_Rec_1302417 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_88362,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_153322,RMVar_hsa_circ_98540,RMVar_hsa_circ_153323 89079 RMVar_ID_89079 Human_SNP_ID_483308559 m1A Human chr11 + 117394410 117394410 117394410 GGCACCTGACCGGAGAGCTGGAGCGCCTGCAGAGGGCCCATGAACGAGAACTGGAGACTGTGAGG GGCACCTGACCGGAGAGCTGGAGCGCCTGCAGTGGGCCCATGAACGAGAACTGGAGACTGTGAGG A T CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117394283..117394481 26863196 MeRIP-seq:(Medium) rs1316877137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226375,Human_RBP_ID_5520976,Human_RBP_ID_5548925,Human_RBP_ID_18974976 Human_Splice_Rec_1302242,Human_Splice_Rec_1302243,Human_Splice_Rec_1302324,Human_Splice_Rec_1302325,Human_Splice_Rec_1302372,Human_Splice_Rec_1302373,Human_Splice_Rec_1302416,Human_Splice_Rec_1302417 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_88362,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_153322,RMVar_hsa_circ_98540,RMVar_hsa_circ_153323 89080 RMVar_ID_89080 Human_SNP_ID_483312417 m1A Human chr11 + 117409726 117409726 117409726 GAGCAGTGTCCTCAGCATCCTGGACAGCCTCAACCCTCAGTCGCCGCCGCCGCTCCTCGCCTCCA GAGCAGTGTCCTCAGCATCCTGGACAGCCTCAGCCCTCAGTCGCCGCCGCCGCTCCTCGCCTCCA A G CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:117409675..117409813 26863196 MeRIP-seq:(Medium) rs1386219058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6048281,Human_RBP_ID_11535572 Human_miRNA_ID_2294093 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_88362,RMVar_hsa_circ_102113,RMVar_hsa_circ_153320,RMVar_hsa_circ_153322,RMVar_hsa_circ_98540,RMVar_hsa_circ_153323,RMVar_hsa_circ_94843,RMVar_hsa_circ_153324 89081 RMVar_ID_89081 Human_SNP_ID_483312431 m1A Human chr11 - 117409747 117409747 117409747 GGGGAGGGAGCTGGGCTGGCATGGAGGCGAGGAGCGGCGGCGGCGACTGAGGGTTGAGGCTGTCC GGGGAGGGAGCTGGGCTGGCATGGAGGCGAGGGGCGGCGGCGGCGACTGAGGGTTGAGGCTGTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117409698..117409781 26863196 MeRIP-seq:(Medium) rs1344104404 Functional Loss SNV dbSNP153 33..33 33 - - - 89082 RMVar_ID_89082 Human_SNP_ID_483495001 m1A Human chr11 + 118126619 118126619 118126619 GCAGAGCAAAGACTTTTCATACAAAGTGGGAAAGAACTGCAATAGAGGCATGTGTCACTGCAGCA GCAGAGCAAAGACTTTTCATACAAAGTGGGAAGGAACTGCAATAGAGGCATGTGTCACTGCAGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118126568..118126707 26863196 MeRIP-seq:(Medium) rs1305655767 Functional Loss SNV dbSNP153 33..33 33 - - - 89083 RMVar_ID_89083 Human_SNP_ID_483563051 m1A Human chr11 + 118397898 118397898 118397898 CCTCAAATCTAAGAGGGCTTCCCATCCTAGATATAAAATAGGTGTTGCCTATTGCTGTGCTTATA CCTCAAATCTAAGAGGGCTTCCCATCCTAGATGTAAAATAGGTGTTGCCTATTGCTGTGCTTATA A G UBE4A Ensembl:ENSG00000110344 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7108613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_389784,Human_RBP_ID_4149037 Human_miRNA_ID_1349493 89084 RMVar_ID_89084 Human_SNP_ID_483563933 m1A Human chr11 - 118401657 118401657 118401657 AAGGTTACGGACAAATTGGGCCATGGTTCTGGAATGGAGAGTCCGTCGCCCCGAACCGCCGGCTG AAGGTTACGGACAAATTGGGCCATGGTTCTGGCATGGAGAGTCCGTCGCCCCGAACCGCCGGCTG T G AP001267.1 Ensembl:ENSG00000254873 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:118401601..118401823 26863196 MeRIP-seq:(Medium) rs1555131065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1304067 89085 RMVar_ID_89085 Human_SNP_ID_483565238 m1A Human chr11 - 118406963 118406963 118406963 CTCAACCTTGGCGTAGTACCAAAATGTGGCCAATCGAGGCTTCGAGTAAGTCACAGCAGCTGGAA CTCAACCTTGGCGTAGTACCAAAATGTGGCCATTCGAGGCTTCGAGTAAGTCACAGCAGCTGGAA T A LOC100131626,LOC100131626:2 RNACentral:URS000075C641,RNACentral:URS000075D191 lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:118406926..118406975 26863196 MeRIP-seq:(Medium) rs1315412876 Functional Loss SNV dbSNP153 33..33 33 - - - 89086 RMVar_ID_89086 Human_SNP_ID_483565258 m1A Human chr11 - 118406991 118406991 118406991 GGATCTCAGCAGGGGTGGGAGGAACCAGCTCAACCTTGGCGTAGTACCAAAATGTGGCCAATCGA GGATCTCAGCAGGGGTGGGAGGAACCAGCTCAGCCTTGGCGTAGTACCAAAATGTGGCCAATCGA T C LOC100131626,LOC100131626:2 RNACentral:URS000075C641,RNACentral:URS000075D191 lincRNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:118406951..118407025 26863196 MeRIP-seq:(Medium) rs1351566454 Functional Loss SNV dbSNP153 33..33 33 - - - 89087 RMVar_ID_89087 Human_SNP_ID_483565741 m1A Human chr11 - 118409022 118409022 118409022 CGACATAAAACCACATCAACACCTCAGTGGCCACCAAACCATTCAGCACAGCTTCCTGAAAAAAG CGACATAAAACCACATCAACACCTCAGTGGCCTCCAAACCATTCAGCACAGCTTCCTGAAAAAAG T A LOC100131626,LOC100131626:2 RNACentral:URS000075C641,RNACentral:URS000075D191 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118409001..118409025 26863196 MeRIP-seq:(Medium) rs782766735 Functional Loss SNV dbSNP153 33..33 33 - - - 89088 RMVar_ID_89088 Human_SNP_ID_483594299 m1A Human chr11 + 118531378 118531361 118531378 CGTAGGGCGAGGGATGGGAGAGAGAACAGGGCAGGAGAGAGGATGGGAACAGGGCAGGAGAGAGA CGTAGGGCGAGGGATG_________________GGAGAGAGGATGGGAACAGGGCAGGAGAGAGA GGGAGAGAGAACAGGGCA G TMEM25 Ensembl:ENSG00000149582 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118531298..118531506 26863196 MeRIP-seq:(Medium) rs1360517153 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_17066942 89089 RMVar_ID_89089 Human_SNP_ID_483603256 m1A Human chr11 + 118565951 118565951 118565951 TAGGCAAAAAGATAAATTTTAAAATTCGCGAGAGTTGCTTCCACTCTCGTGAGACCTCCTGCGCG TAGGCAAAAAGATAAATTTTAAAATTCGCGAGCGTTGCTTCCACTCTCGTGAGACCTCCTGCGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:118565900..118565980;chr11:118565902..118566007 26863196 MeRIP-seq:(Medium) rs1036098779 Functional Loss SNV dbSNP153 33..33 33 - - - 89090 RMVar_ID_89090 Human_SNP_ID_483604860 m1A Human chr11 + 118572462 118572462 118572462 GCAGCGGTTCCTGTCAAGGGGGCAGCAGGTCCAGAGCTGCTGGTGCTCCCGTTCCCCAGACCCTA GCAGCGGTTCCTGTCAAGGGGGCAGCAGGTCCGGAGCTGCTGGTGCTCCCGTTCCCCAGACCCTA A G ARCN1 Ensembl:ENSG00000095139 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118572401..118572575 26863196 MeRIP-seq:(Medium) rs533518004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226309,Human_RBP_ID_389957,Human_RBP_ID_749084,Human_RBP_ID_4149590,Human_RBP_ID_5314464,Human_RBP_ID_8345318,Human_RBP_ID_8774516,Human_RBP_ID_9276083,Human_RBP_ID_9321791,Human_RBP_ID_26886386 Human_Splice_Rec_1304899,Human_Splice_Rec_1304915,Human_Splice_Rec_1304933,Human_Splice_Rec_1304939,Human_Splice_Rec_1304959 Human_miRNA_ID_2300716,Human_miRNA_ID_2303977,Human_miRNA_ID_2307246 RMVar_hsa_circ_112504,RMVar_hsa_circ_153407 89091 RMVar_ID_89091 Human_SNP_ID_483611543 m1A Human chr11 - 118597786 118597786 118597786 ACTCTTATTTTTGGCATCAATCACAGGCAGGCACCACTCCAGGGTATTTCGTCGACTGTCATGTC ACTCTTATTTTTGGCATCAATCACAGGCAGGCGCCACTCCAGGGTATTTCGTCGACTGTCATGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:118597701..118597900 32194978 MeRIP-seq:(Medium) rs782625219 Functional Loss SNV dbSNP153 33..33 33 - - - 89092 RMVar_ID_89092 Human_SNP_ID_483615876 m1A Human chr11 - 118613869 118613869 118613869 CTCACCTGCACCATGGTCTGGGTCTGGCATCCAGGGCCTATTTGGTTCCTATTGAGAGCGTCCAT CTCACCTGCACCATGGTCTGGGTCTGGCATCCCGGGCCTATTTGGTTCCTATTGAGAGCGTCCAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118613782..118613883 26863196 MeRIP-seq:(Medium) rs781834869 Functional Loss SNV dbSNP153 33..33 33 - - - 89093 RMVar_ID_89093 Human_SNP_ID_483619070 m1A Human chr11 + 118627360 118627360 118627360 GGGAACCACACCCCACAGACTGCAACACGGGGACCCTCTGCCTGTGCCAGCCACAGTTCCCTGGT GGGAACCACACCCCACAGACTGCAACACGGGGGCCCTCTGCCTGTGCCAGCCACAGTTCCCTGGT A G PHLDB1 Ensembl:ENSG00000019144 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118627310..118627461 32194978 MeRIP-seq:(Medium) rs781898425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8345342 Human_Splice_Rec_1304974,Human_Splice_Rec_1305018,Human_Splice_Rec_1305030,Human_Splice_Rec_1305070,Human_Splice_Rec_1305114,Human_Splice_Rec_1305154,Human_Splice_Rec_1305166,Human_Splice_Rec_1305208,Human_Splice_Rec_1305216,Human_Splice_Rec_1305220 Human_miRNA_ID_691619,Human_miRNA_ID_1015412,Human_miRNA_ID_1301445 89094 RMVar_ID_89094 Human_SNP_ID_483619297 m1A Human chr11 - 118627986 118627986 118627986 GGAGTGTGCCAATCTTGTTTCGGGGAGCAGGGACTGGAGGCTGAAACTTGGGGCTGCCAGGAATG GGAGTGTGCCAATCTTGTTTCGGGGAGCAGGGTCTGGAGGCTGAAACTTGGGGCTGCCAGGAATG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118627887..118627985 26863196 MeRIP-seq:(Medium) rs1565431327 Functional Loss SNV dbSNP153 33..33 33 - - - 89095 RMVar_ID_89095 Human_SNP_ID_483619360 m1A Human chr11 - 118628110 118628110 118628110 GGCTGCAGGGTACGGGTGGCTAACCCATCTGAAAATGTTCGGCCCACCAGTTGGCGTGAGGGGCT GGCTGCAGGGTACGGGTGGCTAACCCATCTGAGAATGTTCGGCCCACCAGTTGGCGTGAGGGGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118628059..118630037 32194978 MeRIP-seq:(Medium) rs782181449 Functional Loss SNV dbSNP153 33..33 33 - - - 89096 RMVar_ID_89096 Human_SNP_ID_483623313 m1A Human chr11 - 118643881 118643881 118643881 AGCCACGCTGAGCTGGGAGGAGGAGGAGGAAGAGCCAGAGGAGGAGGGGAGGGGGCCGCTGCGGG AGCCACGCTGAGCTGGGAGGAGGAGGAGGAAGTGCCAGAGGAGGAGGGGAGGGGGCCGCTGCGGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118643830..118644036 32194978 MeRIP-seq:(Medium) rs1555123898 Functional Loss SNV dbSNP153 33..33 33 - - - 89097 RMVar_ID_89097 Human_SNP_ID_483623856 m1A Human chr11 - 118645585 118645585 118645585 CCCCCGGTGGAGATGCTGGTCTCCATGCTGTCAGAGCTCTCCAGACTCAGCGTATCATAGGCGTG CCCCCGGTGGAGATGCTGGTCTCCATGCTGTCGGAGCTCTCCAGACTCAGCGTATCATAGGCGTG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:118645557..118645649 26863410 MeRIP-seq:(Medium) rs888027651 Functional Loss SNV dbSNP153 33..33 33 - - - 89098 RMVar_ID_89098 Human_SNP_ID_483624542 m1A Human chr11 + 118648012 118648012 118648012 GCGTGAGCAGGTAGAACGGAGGCTGCAGAGTGAGAGTGCCCGGAGGCAGCAGCTGGTCGAGAAGG GCGTGAGCAGGTAGAACGGAGGCTGCAGAGTGCGAGTGCCCGGAGGCAGCAGCTGGTCGAGAAGG A C PHLDB1 Ensembl:ENSG00000019144 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118647838..118648075 26863196 MeRIP-seq:(Medium) rs200883102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_866192,Human_RBP_ID_3941284,Human_RBP_ID_5343004,Human_RBP_ID_9362986,Human_RBP_ID_18972804,Human_RBP_ID_22895772,Human_RBP_ID_26319299 Human_Splice_Rec_1304998,Human_Splice_Rec_1304999,Human_Splice_Rec_1305052,Human_Splice_Rec_1305053,Human_Splice_Rec_1305094,Human_Splice_Rec_1305095,Human_Splice_Rec_1305136,Human_Splice_Rec_1305137,Human_Splice_Rec_1305188,Human_Splice_Rec_1305189,Human_Splice_Rec_1305248,Human_Splice_Rec_1305249,Human_Splice_Rec_1305278,Human_Splice_Rec_1305279,Human_Splice_Rec_1305302,Human_Splice_Rec_1305303,Human_Splice_Rec_1305330,Human_Splice_Rec_1305331,Human_Splice_Rec_1305366,Human_Splice_Rec_1305367,Human_Splice_Rec_1305388,Human_Splice_Rec_1305389,Human_Splice_Rec_1305412,Human_Splice_Rec_1305413,Human_Splice_Rec_1305417 RMVar_hsa_circ_8105,RMVar_hsa_circ_29736 89099 RMVar_ID_89099 Human_SNP_ID_483635939 m1A Human chr11 - 118691150 118691149 118691150 AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGGAGGTGATGTGTGAGCAGAATTGTGGCAGGAACC AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGGCCGTGATGTGTGAGCAGAATTGTGGCAGGAACC CT GG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118690984..118691258 26863196 MeRIP-seq:(Medium) rs386757969 Functional Loss MNV dbSNP153 33..34 33 - - - 89100 RMVar_ID_89100 Human_SNP_ID_483635940 m1A Human chr11 - 118691150 118691149 118691150 AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGGAGGTGATGTGTGAGCAGAATTGTGGCAGGAACC AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGG_GGTGATGTGTGAGCAGAATTGTGGCAGGAACC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118690984..118691258 26863196 MeRIP-seq:(Medium) rs1555148674 Functional Loss DEL dbSNP153 33..33 33 - - - 89101 RMVar_ID_89101 Human_SNP_ID_483635944 m1A Human chr11 - 118691150 118691150 118691150 AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGGAGGTGATGTGTGAGCAGAATTGTGGCAGGAACC AGAGAGGATGGGGAGGGAAGGTGTCTCTGAGGCGGTGATGTGTGAGCAGAATTGTGGCAGGAACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118690984..118691258 26863196 MeRIP-seq:(Medium) rs10790258 Functional Loss SNV dbSNP153 33..33 33 - - - 89102 RMVar_ID_89102 Human_SNP_ID_483643581 m1A Human chr11 + 118719922 118719922 118719922 GGCTTTGGATTGGGAAGAAGGGCAGCAATAAGATGCAGCTGTAATCCAGGAATAGTCAGGGAAGC GGCTTTGGATTGGGAAGAAGGGCAGCAATAAGGTGCAGCTGTAATCCAGGAATAGTCAGGGAAGC A G AP002954.1 Ensembl:ENSG00000255422 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:118719880..118720212 26863196 MeRIP-seq:(Medium) rs1268735760 Functional Loss SNV dbSNP153 33..33 33 - - - 89103 RMVar_ID_89103 Human_SNP_ID_483663542 m1A Human chr11 - 118786125 118786125 118786125 GAGGAGGGGGCACACAGACACAGCAACAGATGAACCAGCTGAAAAACACCAACACAATCAATAAT GAGGAGGGGGCACACAGACACAGCAACAGATGGACCAGCTGAAAAACACCAACACAATCAATAAT T C DDX6 Ensembl:ENSG00000110367 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:118786076..118786150 26863196 MeRIP-seq:(Medium) rs1415963087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226134,Human_RBP_ID_1776118,Human_RBP_ID_18525758,Human_RBP_ID_22435638,Human_RBP_ID_27409294 Human_Splice_Rec_1305545,Human_Splice_Rec_1305571,Human_Splice_Rec_1305597,Human_Splice_Rec_1305617,Human_Splice_Rec_1305641,Human_Splice_Rec_1305643 RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_88517,RMVar_hsa_circ_276233,RMVar_hsa_circ_273228,RMVar_hsa_circ_282671,RMVar_hsa_circ_153440,RMVar_hsa_circ_337817,RMVar_hsa_circ_104808,RMVar_hsa_circ_153442,RMVar_hsa_circ_153443,RMVar_hsa_circ_153441 89104 RMVar_ID_89104 Human_SNP_ID_483665549 m1A Human chr11 - 118791838 118791824 118791838 GCCAGGCGCGCCCTACAGGCTCGCCCCGTCCCACCGCGCAGCGCCCCCCGCGCACTCTCTGGAGT GCCAGGCGCGCCCTACAGGCTCGCCCCGTCCC______________CCCGCGCACTCTCTGGAGT GGGGCGCTGCGCGGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118791740..118792443 26863196 MeRIP-seq:(Medium) rs1287725232 Functional Loss DEL dbSNP153 33..46 33 - - - 89105 RMVar_ID_89105 Human_SNP_ID_483665553 m1A Human chr11 - 118791838 118791838 118791838 GCCAGGCGCGCCCTACAGGCTCGCCCCGTCCCACCGCGCAGCGCCCCCCGCGCACTCTCTGGAGT GCCAGGCGCGCCCTACAGGCTCGCCCCGTCCCCCCGCGCAGCGCCCCCCGCGCACTCTCTGGAGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118791740..118792443 26863196 MeRIP-seq:(Medium) rs1031436532 Functional Loss SNV dbSNP153 33..33 33 - - - 89106 RMVar_ID_89106 Human_SNP_ID_483665605 m1A Human chr11 + 118791970 118791970 118791970 AGGGTGCACCTGGGCGGGGGAAGTCTTCGGGCATGAGGGCGCGCCTGCGGGTGGTATGGGGGGGT AGGGTGCACCTGGGCGGGGGAAGTCTTCGGGCCTGAGGGCGCGCCTGCGGGTGGTATGGGGGGGT A C AP004609.5 Ensembl:ENSG00000278376 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118791609..118792556 26863196 MeRIP-seq:(Medium) rs1275132175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8174762,Human_RBP_ID_9415698 89107 RMVar_ID_89107 Human_SNP_ID_483692115 m1A Human chr11 + 118897000 118897000 118897000 CTCTCCTGGGTAGGAGCAGGGAGCCAAGGGGGAGGCAGTGGCTGTGCCTGGGTGGGCACAGACAG CTCTCCTGGGTAGGAGCAGGGAGCCAAGGGGGGGGCAGTGGCTGTGCCTGGGTGGGCACAGACAG A G CXCR5 Ensembl:ENSG00000160683 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:118896951..118897000 26863196 MeRIP-seq:(Medium) rs1209331471 Functional Loss SNV dbSNP153 33..33 33 - - - 89108 RMVar_ID_89108 Human_SNP_ID_483692836 m1A Human chr11 - 118898960 118898960 118898960 CCGAGCTGAGCGAGGTGATCCGGCCCACCCCAACGGGGATCCCCGAGTTCGACTTGTCGAGGATC CCGAGCTGAGCGAGGTGATCCGGCCCACCCCAGCGGGGATCCCCGAGTTCGACTTGTCGAGGATC T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118898909..118899097 32194978 MeRIP-seq:(Medium) rs773305789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126780,Human_RBP_ID_8345403 89109 RMVar_ID_89109 Human_SNP_ID_483693084 m1A Human chr11 - 118899503 118899503 118899503 TGACCCCCTGTCTTCTATTCCCTACAGGGATCAGCAACAGCCAGCCCAGCCAGATGCACCTGAAC TGACCCCCTGTCTTCTATTCCCTACAGGGATCGGCAACAGCCAGCCCAGCCAGATGCACCTGAAC T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118898700..118899537 26863196 MeRIP-seq:(Medium) rs1162069113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1305664,Human_Splice_Rec_1305678 89110 RMVar_ID_89110 Human_SNP_ID_483693306 m1A Human chr11 + 118900072 118900071 118900073 CGTACTTGGACATCTGGGTCATCATCAGTGACAGGGGGTTCTGGGAAGGTGTGGGGTCTGGGGAG CGTACTTGGACATCTGGGTCATCATCAGTGAC__GGGGTTCTGGGAAGGTGTGGGGTCTGGGGAG CAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:118900026..118900202 26863196 MeRIP-seq:(Medium) rs1274382207 Functional Loss DEL dbSNP153 33..34 33 - - - 89111 RMVar_ID_89111 Human_SNP_ID_483693336 m1A Human chr11 - 118900126 118900126 118900126 ACCTCCCGCCAACCCTCCCAGCGGCCTCATGAACCCCAGCCTACCATTCACTTCCTCCCCAGACC ACCTCCCGCCAACCCTCCCAGCGGCCTCATGAGCCCCAGCCTACCATTCACTTCCTCCCCAGACC T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:118899901..118900217 26863196 MeRIP-seq:(Medium) rs1287130045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385743,Human_RBP_ID_5126784,Human_RBP_ID_17074260,Human_RBP_ID_17350368,Human_RBP_ID_18932966,Human_RBP_ID_27409332,Human_RBP_ID_27556516 Human_Splice_Rec_1305662,Human_Splice_Rec_1305676,Human_Splice_Rec_1305680 Human_miRNA_ID_1355826 89112 RMVar_ID_89112 Human_SNP_ID_483693609 m1A Human chr11 + 118900827 118900827 118900827 AGGGAGGAGCCGAGGACCTGGGGCGACTTGAGAGGTCCTGGCGGGTTGGCAGAAGGCAAGGGCAC AGGGAGGAGCCGAGGACCTGGGGCGACTTGAGTGGTCCTGGCGGGTTGGCAGAAGGCAAGGGCAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118900776..118900887 26863196 MeRIP-seq:(Medium) rs574277827 Functional Loss SNV dbSNP153 33..33 33 - - - 89113 RMVar_ID_89113 Human_SNP_ID_483693850 m1A Human chr11 - 118901423 118901423 118901423 CACCCATGGGGCCAGGCAACCTCAACATGAACATGAATGTCAACATGAACATGAACATGAACCTG CACCCATGGGGCCAGGCAACCTCAACATGAACCTGAATGTCAACATGAACATGAACATGAACCTG T G BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118901332..118901882 32194978 MeRIP-seq:(Medium) rs1289077527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73107 89114 RMVar_ID_89114 Human_SNP_ID_483694156 m1A Human chr11 + 118902175 118902175 118902175 TCCGCCGTTTCTCTTCGTAGTACTCCTCCTGCAGCTTGCGCCAGGCCACCTGCTCAGGCGTGAGG TCCGCCGTTTCTCTTCGTAGTACTCCTCCTGCGGCTTGCGCCAGGCCACCTGCTCAGGCGTGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118902090..118902291 26863196 MeRIP-seq:(Medium) rs1366493384 Functional Loss SNV dbSNP153 33..33 33 - - - 89115 RMVar_ID_89115 Human_SNP_ID_483694296 m1A Human chr11 - 118902424 118902424 118902424 CTTCCTCAAGGGGCCCCCAGGAGGAGCGGGTGAGGGGGGCCCACCAGCACAAGCCCCCCCTCCCC CTTCCTCAAGGGGCCCCCAGGAGGAGCGGGTGGGGGGGGCCCACCAGCACAAGCCCCCCCTCCCC T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118902379..118902630 32194978 MeRIP-seq:(Medium) rs764315126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73107 89116 RMVar_ID_89116 Human_SNP_ID_483694446 m1A Human chr11 - 118902752 118902752 118902752 CTCTGCCCCCAGAGGGGCCTCCTGAGGACAGCAGTCAGGACCTGGCCCCCAACTCGGTGGGAGCT CTCTGCCCCCAGAGGGGCCTCCTGAGGACAGCGGTCAGGACCTGGCCCCCAACTCGGTGGGAGCT T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:118902701..118902775 26863196 MeRIP-seq:(Medium) rs1565619047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73107 89117 RMVar_ID_89117 Human_SNP_ID_483696200 m1A Human chr11 + 118908544 118908535 118908544 GATTGGGCCCCGCCATTCCCTGTCTTGCCATGATTGGTCAATTTATTTTCTGGGTGCATTGGCTT GATTGGGCCCCGCCATTCCCTGTC_________TTGGTCAATTTATTTTCTGGGTGCATTGGCTT CTTGCCATGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118908494..118908653 26863196 MeRIP-seq:(Medium) rs774488482 Functional Loss DEL dbSNP153 25..33 33 - - - 89118 RMVar_ID_89118 Human_SNP_ID_483696204 m1A Human chr11 + 118908544 118908544 118908544 GATTGGGCCCCGCCATTCCCTGTCTTGCCATGATTGGTCAATTTATTTTCTGGGTGCATTGGCTT GATTGGGCCCCGCCATTCCCTGTCTTGCCATGCTTGGTCAATTTATTTTCTGGGTGCATTGGCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:118908494..118908653 26863196 MeRIP-seq:(Medium) rs1403176135 Functional Loss SNV dbSNP153 33..33 33 - - - 89119 RMVar_ID_89119 Human_SNP_ID_483696608 m1A Human chr11 + 118909807 118909807 118909807 TAGCCCACTGGTGGCCTGGGAGCCAGGTGCCCAGGGCGGCTCCTCTCCTGGCCAGCACAGCTTGG TAGCCCACTGGTGGCCTGGGAGCCAGGTGCCCCGGGCGGCTCCTCTCCTGGCCAGCACAGCTTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:118909805..118909954;chr11:118909802..118909937 26863196 MeRIP-seq:(Medium) rs1036682228 Functional Loss SNV dbSNP153 33..33 33 - - - 89120 RMVar_ID_89120 Human_SNP_ID_483696986 m1A Human chr11 + 118910936 118910936 118910936 GGAGCCCAGGAAGCTAGAGGCGCGCCGAGGCCAGGGAAGCGCCGCCGGAGCGGGAGGCGCGGAGA GGAGCCCAGGAAGCTAGAGGCGCGCCGAGGCCGGGGAAGCGCCGCCGGAGCGGGAGGCGCGGAGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:118910896..118911080 26863196 MeRIP-seq:(Medium) rs956639991 Functional Loss SNV dbSNP153 33..33 33 - - - 89121 RMVar_ID_89121 Human_SNP_ID_483696987 m1A Human chr11 + 118910936 118910936 118910936 GGAGCCCAGGAAGCTAGAGGCGCGCCGAGGCCAGGGAAGCGCCGCCGGAGCGGGAGGCGCGGAGA GGAGCCCAGGAAGCTAGAGGCGCGCCGAGGCCTGGGAAGCGCCGCCGGAGCGGGAGGCGCGGAGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:118910896..118911080 26863196 MeRIP-seq:(Medium) rs956639991 Functional Loss SNV dbSNP153 33..33 33 - - - 89122 RMVar_ID_89122 Human_SNP_ID_483697898 m1A Human chr11 - 118914404 118914404 118914404 CCTCTGCCTCTGGCTGTACCTGGGGAGAGAGCAGAGCAGGCAGGCAGGCGGGCGGGCGCTGGGTG CCTCTGCCTCTGGCTGTACCTGGGGAGAGAGCGGAGCAGGCAGGCAGGCGGGCGGGCGCTGGGTG T C BCL9L Ensembl:ENSG00000186174 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118914402..118914541 26863196 MeRIP-seq:(Medium) rs889576708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18456980 89123 RMVar_ID_89123 Human_SNP_ID_483699716 m1A Human chr11 - 118921592 118921592 118921592 CCCTGGTGTTTTATTCTAGGCCCCCTTCCACCAGAGCTGGGACTCCCTCTGTCCGTTCCCGTTCC CCCTGGTGTTTTATTCTAGGCCCCCTTCCACCGGAGCTGGGACTCCCTCTGTCCGTTCCCGTTCC T C BCL9L Ensembl:ENSG00000186174 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:118921565..118921692 26863196 MeRIP-seq:(Medium) rs1227144697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3385773 89124 RMVar_ID_89124 Human_SNP_ID_483700783 m1A Human chr11 - 118925877 118925877 118925877 GAGCCGAGTGGAGGGGCAAGCGAGGCTCCGGCAGCGCAGGGGAGCCCGGGGAGGCGGCGGCGCGC GAGCCGAGTGGAGGGGCAAGCGAGGCTCCGGCTGCGCAGGGGAGCCCGGGGAGGCGGCGGCGCGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr11:118925750..118925908;chr11:118925669..118926034 26863196 MeRIP-seq:(Medium) rs1252856349 Functional Loss SNV dbSNP153 33..33 33 - - - 89125 RMVar_ID_89125 Human_SNP_ID_483719816 m1A Human chr11 + 118997691 118997691 118997691 ATGAGTGACGGGGATCAGGTGCTGACCGCGCTACTTAACACCCGTGCAACCCTCCTCAAAGCTCC ATGAGTGACGGGGATCAGGTGCTGACCGCGCTGCTTAACACCCGTGCAACCCTCCTCAAAGCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118997213..118997761 26863196 MeRIP-seq:(Medium) rs1264000345 Functional Loss SNV dbSNP153 33..33 33 - - - 89126 RMVar_ID_89126 Human_SNP_ID_483723390 m1A Human chr11 + 119010227 119010227 119010227 CTGGATTCTTCTGAGGATGTGAAGTAATGGAAACAGTAAGACTGTTCCAGACTAGGGGAAGACTA CTGGATTCTTCTGAGGATGTGAAGTAATGGAAGCAGTAAGACTGTTCCAGACTAGGGGAAGACTA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119010191..119010305 26863196 MeRIP-seq:(Medium) rs1310827932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541018 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 89127 RMVar_ID_89127 Human_SNP_ID_483726066 m1A Human chr11 + 119017477 119017477 119017477 AGTTTATAGTTGGGAACTTCCTTACAGAGTTTATCATAGGTAGCTTTGTCAAACAAGACTAAGTT AGTTTATAGTTGGGAACTTCCTTACAGAGTTTGTCATAGGTAGCTTTGTCAAACAAGACTAAGTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:119017426..119017559 32194978 MeRIP-seq:(Medium) rs1397546127 Functional Loss SNV dbSNP153 33..33 33 - - - 89128 RMVar_ID_89128 Human_SNP_ID_483726297 m1A Human chr11 - 119018055 119018055 119018055 AGGACCTGGTTGCATTCCCGCTGCCCTCCTACAGCCGCCTAAGGACGACAAGAAGAAGAAGGACG AGGACCTGGTTGCATTCCCGCTGCCCTCCTACTGCCGCCTAAGGACGACAAGAAGAAGAAGGACG T A RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:119018026..119018075;chr11:119017972..119018092 26863196 MeRIP-seq:(Medium) rs879190073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_869405,Human_RBP_ID_2253112,Human_RBP_ID_26886617,Human_RBP_ID_27409422 Human_Splice_Rec_1305859,Human_Splice_Rec_1305867,Human_Splice_Rec_1305879 RMVar_hsa_circ_124755,RMVar_hsa_circ_153450 89129 RMVar_ID_89129 Human_SNP_ID_483726399 m1A Human chr11 - 119018278 119018278 119018278 TCTGCTGCTATTCTCCGAGCTTCGCAATGGTAAGCTTCAGGGGTGTGAAGTCGCCGGCGTTCTTG TCTGCTGCTATTCTCCGAGCTTCGCAATGGTAGGCTTCAGGGGTGTGAAGTCGCCGGCGTTCTTG T C RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr11:119018276..119018400;chr11:119018276..119018350 26863196,32194978 MeRIP-seq:(Medium) rs909685982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4150017,Human_RBP_ID_8345447,Human_RBP_ID_18603885,Human_RBP_ID_22158912,Human_RBP_ID_22789729,Human_RBP_ID_26410307 RMVar_hsa_circ_124755,RMVar_hsa_circ_153450 89130 RMVar_ID_89130 Human_SNP_ID_483726731 m1A Human chr11 - 119018831 119018831 119018831 GCGTAGCTGTCCAACTGGTAAATCAAGCCGCCAGCTTTGTTCACCACATACACACTAAAAATCGC GCGTAGCTGTCCAACTGGTAAATCAAGCCGCCCGCTTTGTTCACCACATACACACTAAAAATCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119018751..119018975 26863196 MeRIP-seq:(Medium) rs782543416 Functional Loss SNV dbSNP153 33..33 33 - - - 89131 RMVar_ID_89131 Human_SNP_ID_483735276 m1A Human chr11 - 119045609 119045609 119045609 AGAACAATCGACAGGACAGAAGCGGCCTTTGAAGAACGACGAACTATAACCCCCACCTCTGTTTT AGAACAATCGACAGGACAGAAGCGGCCTTTGAGGAACGACGAACTATAACCCCCACCTCTGTTTT T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119045558..119045669 26863196 MeRIP-seq:(Medium) rs1341239590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_390226,Human_RBP_ID_871551,Human_RBP_ID_5165454,Human_RBP_ID_5548948,Human_RBP_ID_11541408,Human_RBP_ID_22755033 Human_Splice_Rec_1306280,Human_Splice_Rec_1306374,Human_Splice_Rec_1306424,Human_Splice_Rec_1306510 89132 RMVar_ID_89132 Human_SNP_ID_483735586 m1A Human chr11 + 119046481 119046480 119046481 TCTGCATCTTCAGTCTGGCCTAGAAGGAAACCAGGGGTAAGACATAGCCTCAGGAAGGAAAGGAG TCTGCATCTTCAGTCTGGCCTAGAAGGAAACC_GGGGTAAGACATAGCCTCAGGAAGGAAAGGAG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119046480..119046587 26863196 MeRIP-seq:(Medium) rs1441872788 Functional Loss DEL dbSNP153 33..33 33 - - - 89133 RMVar_ID_89133 Human_SNP_ID_483735685 m1A Human chr11 - 119046696 119046696 119046696 CATTGAAGCTAAGATGATGGCCCTGGACCGAGAGGTGCAGTATCTGCTCAATAAGGCCAAGTTTA CATTGAAGCTAAGATGATGGCCCTGGACCGAGTGGTGCAGTATCTGCTCAATAAGGCCAAGTTTA T A HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119046551..119046825 32194978 MeRIP-seq:(Medium) rs782342122 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_390229,Human_RBP_ID_749847,Human_RBP_ID_1776174,Human_RBP_ID_3941289,Human_RBP_ID_6049883,Human_RBP_ID_8774536,Human_RBP_ID_9254734,Human_RBP_ID_9276109,Human_RBP_ID_17790953,Human_RBP_ID_22754372,Human_RBP_ID_26805216 Human_Splice_Rec_1306458 Human_miRNA_ID_2750760 RMVar_hsa_circ_62478 89134 RMVar_ID_89134 Human_SNP_ID_483736079 m1A Human chr11 + 119048028 119048028 119048028 GTTCGGGCCACTTCTTGCGCTCCTCTACCCGAAAAAACAGCCCTTGGCACAGCTTCCTCAGCTCA GTTCGGGCCACTTCTTGCGCTCCTCTACCCGAGAAAACAGCCCTTGGCACAGCTTCCTCAGCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119047951..119048100 26863196 MeRIP-seq:(Medium) rs1260794182 Functional Loss SNV dbSNP153 33..33 33 - - - 89135 RMVar_ID_89135 Human_SNP_ID_483736270 m1A Human chr11 - 119048494 119048494 119048494 GAACGGGAAAAAGCTGCCAACAGCTTGGAAGCATTCATATTTGAGACCCAGGTCAGTGGGCAGGA GAACGGGAAAAAGCTGCCAACAGCTTGGAAGCGTTCATATTTGAGACCCAGGTCAGTGGGCAGGA T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs568922 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_390234 Human_Splice_Rec_1306266,Human_Splice_Rec_1306267,Human_Splice_Rec_1306360,Human_Splice_Rec_1306361,Human_Splice_Rec_1306410,Human_Splice_Rec_1306411,Human_Splice_Rec_1306496,Human_Splice_Rec_1306497,Human_Splice_Rec_1306514,Human_Splice_Rec_1306548,Human_Splice_Rec_1306549 Human_miRNA_ID_473471,Human_miRNA_ID_1099548 GWAS_ID_11571,GWAS_ID_11572,GWAS_ID_11573,GWAS_ID_11574,GWAS_ID_11575,GWAS_ID_11576,GWAS_ID_11577,GWAS_ID_11578 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 89136 RMVar_ID_89136 Human_SNP_ID_483736412 m1A Human chr11 - 119048884 119048884 119048884 TTCCTGACACCCCTGACTCTTCCCACCCAGAAACCAAGTGAGAAGGCAGAGGCAGGGCCTGAGGG TTCCTGACACCCCTGACTCTTCCCACCCAGAAGCCAAGTGAGAAGGCAGAGGCAGGGCCTGAGGG T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119048721..119048901 26863196 MeRIP-seq:(Medium) rs782646161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226707 Human_Splice_Rec_1306264,Human_Splice_Rec_1306358,Human_Splice_Rec_1306408,Human_Splice_Rec_1306494,Human_Splice_Rec_1306546 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 89137 RMVar_ID_89137 Human_SNP_ID_483736501 m1A Human chr11 - 119049172 119049172 119049172 GGAGGAAGAGGAGAGCCCTGCAGAGGGGAGCAAGGACGAGCCTGGGGAGCAGGTGGAGCTCAAGG GGAGGAAGAGGAGAGCCCTGCAGAGGGGAGCAGGGACGAGCCTGGGGAGCAGGTGGAGCTCAAGG T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:119049001..119049225;chr11:119048994..119049225 26863196 MeRIP-seq:(Medium) rs1373996333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_749854,Human_RBP_ID_807412,Human_RBP_ID_871559,Human_RBP_ID_5139506,Human_RBP_ID_6049888,Human_RBP_ID_9276117,Human_RBP_ID_9363019,Human_RBP_ID_22433999,Human_RBP_ID_22754384,Human_RBP_ID_22895219,Human_RBP_ID_26319316 Human_Splice_Rec_1306262,Human_Splice_Rec_1306312,Human_Splice_Rec_1306406,Human_Splice_Rec_1306456,Human_Splice_Rec_1306582 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 89138 RMVar_ID_89138 Human_SNP_ID_483737504 m1A Human chr11 + 119052082 119052080 119052082 CAGGCAGAACTCAGCCAAGCGCTCTAGCCCCCACACTCACTTGCCCACGGCCTTCAGCAGCACCT CAGGCAGAACTCAGCCAAGCGCTCTAGCCCC__CACTCACTTGCCCACGGCCTTCAGCAGCACCT CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119052077..119052164 26863196 MeRIP-seq:(Medium) rs782192495 Functional Loss DEL dbSNP153 32..33 33 - - - 89139 RMVar_ID_89139 Human_SNP_ID_483737738 m1A Human chr11 + 119052745 119052745 119052745 CGCGGGTTCTCCCGCACATCCTTTGCTCTCTGACCCTTGCGCTGCTCATTGAAAAGCCCAGCCAG CGCGGGTTCTCCCGCACATCCTTTGCTCTCTGGCCCTTGCGCTGCTCATTGAAAAGCCCAGCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119052695..119052766 26863196 MeRIP-seq:(Medium) rs1165970454 Functional Loss SNV dbSNP153 33..33 33 - - - 89140 RMVar_ID_89140 Human_SNP_ID_483738715 m1A Human chr11 - 119055841 119055841 119055841 AGCTAACTGACAAACCTCTTTTCCCTTCAGATACACTGGCAGTGATGTCTGTGGACCTGGGCAGT AGCTAACTGACAAACCTCTTTTCCCTTCAGATGCACTGGCAGTGATGTCTGTGGACCTGGGCAGT T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119055801..119055850 26863196 MeRIP-seq:(Medium) rs1359800525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184444,Human_RBP_ID_8940580,Human_RBP_ID_17804816,Human_RBP_ID_22434020 Human_Splice_Rec_1306234,Human_Splice_Rec_1306235,Human_Splice_Rec_1306284,Human_Splice_Rec_1306285,Human_Splice_Rec_1306318,Human_Splice_Rec_1306319,Human_Splice_Rec_1306330,Human_Splice_Rec_1306331,Human_Splice_Rec_1306378,Human_Splice_Rec_1306379,Human_Splice_Rec_1306428,Human_Splice_Rec_1306429,Human_Splice_Rec_1306466,Human_Splice_Rec_1306467,Human_Splice_Rec_1306554,Human_Splice_Rec_1306555,Human_Splice_Rec_1306592,Human_Splice_Rec_1306593,Human_Splice_Rec_1306604,Human_Splice_Rec_1306605,Human_Splice_Rec_1306624,Human_Splice_Rec_1306625,Human_Splice_Rec_1306634,Human_Splice_Rec_1306635,Human_Splice_Rec_1306642,Human_Splice_Rec_1306643,Human_Splice_Rec_1306652,Human_Splice_Rec_1306653,Human_Splice_Rec_1306658,Human_Splice_Rec_1306666,Human_Splice_Rec_1306667,Human_Splice_Rec_1306676,Human_Splice_Rec_1306677,Human_Splice_Rec_1306684 RMVar_hsa_circ_66064 89141 RMVar_ID_89141 Human_SNP_ID_483739192 m1A Human chr11 - 119057072 119057072 119057072 CGCGGGTGGGGGGCGCTGCCGGCCTCGTGGGTACGTTCGTGCCGCGTCTGTCCCAGAGCTGGGGC CGCGGGTGGGGGGCGCTGCCGGCCTCGTGGGTTCGTTCGTGCCGCGTCTGTCCCAGAGCTGGGGC T A HYOU1 Ensembl:ENSG00000149428 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:119056875..119057184;chr11:119056851..119057168 26863196 MeRIP-seq:(Medium) rs943639321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227740,Human_RBP_ID_751337,Human_RBP_ID_4184448,Human_RBP_ID_5461196,Human_RBP_ID_8774554,Human_RBP_ID_18416674,Human_RBP_ID_22434022 Human_Splice_Rec_1306231,Human_Splice_Rec_1306281,Human_Splice_Rec_1306327,Human_Splice_Rec_1306425,Human_Splice_Rec_1306461,Human_Splice_Rec_1306515,Human_Splice_Rec_1306639,Human_Splice_Rec_1306649,Human_Splice_Rec_1306661,Human_Splice_Rec_1306681 89142 RMVar_ID_89142 Human_SNP_ID_483747598 m1A Human chr11 + 119085002 119085002 119085002 CCGGCTTCCCGGGGCCGGGGGACCTTAGCGGCACCCACACACAGCCTACTTTCCAAGCGGAGCCA CCGGCTTCCCGGGGCCGGGGGACCTTAGCGGCTCCCACACACAGCCTACTTTCCAAGCGGAGCCA A T HMBS Ensembl:ENSG00000256269 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:119084901..119085075 26863410 MeRIP-seq:(Medium) rs782213223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185437,Human_RBP_ID_22895780 Human_Splice_Rec_1306797,Human_Splice_Rec_1306805,Human_Splice_Rec_1306809,Human_Splice_Rec_1306827,Human_Splice_Rec_1306853,Human_Splice_Rec_1306929,Human_Splice_Rec_1306941,Human_Splice_Rec_1306965,Human_Splice_Rec_1306995,Human_Splice_Rec_1307017,Human_Splice_Rec_1307037,Human_Splice_Rec_1307061,Human_Splice_Rec_1307075,Human_Splice_Rec_1307097,Human_Splice_Rec_1307109,Human_Splice_Rec_1307123 RMVar_hsa_circ_106536,RMVar_hsa_circ_153475 89143 RMVar_ID_89143 Human_SNP_ID_483749920 m1A Human chr11 - 119092486 119092486 119092486 GCCTCAGGAAGGCCCTTTCAGCGATGCAGCGAAGCAGAGTCTCGGGATCGTGCAGCACACCCACC GCCTCAGGAAGGCCCTTTCAGCGATGCAGCGACGCAGAGTCTCGGGATCGTGCAGCACACCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119092436..119092539 26863196 MeRIP-seq:(Medium) rs118204099 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_503 GWAS_ID_11579 89144 RMVar_ID_89144 Human_SNP_ID_483750521 m1A Human chr11 - 119094068 119094068 119094068 GCCAGGCCTGTCGGGCCCCCCGACGCCGCCCCATTTCCCTTCCAGCAAACTCAACTCGGCAATCC GCCAGGCCTGTCGGGCCCCCCGACGCCGCCCCGTTTCCCTTCCAGCAAACTCAACTCGGCAATCC T C H2AX Ensembl:ENSG00000188486 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119094025..119094518 32194978 MeRIP-seq:(Medium) rs907206946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32693,Human_RBP_ID_390282,Human_RBP_ID_8246267,Human_RBP_ID_17231167,Human_RBP_ID_17347620,Human_RBP_ID_17463321,Human_RBP_ID_17790979,Human_RBP_ID_18525759,Human_RBP_ID_27198591,Human_RBP_ID_27409471 Human_miRNA_ID_1656425 89145 RMVar_ID_89145 Human_SNP_ID_483750699 m1A Human chr11 - 119094665 119094665 119094665 CCTTCCGGATGCGGCTTGGGCGCTCTTCGGGGACCTCCGTGGCGCGGAAGACCCGAGCCTGCCGG CCTTCCGGATGCGGCTTGGGCGCTCTTCGGGGGCCTCCGTGGCGCGGAAGACCCGAGCCTGCCGG T C H2AX Ensembl:ENSG00000188486 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119094619..119094712 26863196 MeRIP-seq:(Medium) rs920397393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_390293,Human_RBP_ID_986046,Human_RBP_ID_5167277,Human_RBP_ID_6049972,Human_RBP_ID_8345513,Human_RBP_ID_8767344,Human_RBP_ID_9321802,Human_RBP_ID_11541775,Human_RBP_ID_17790993,Human_RBP_ID_18432410,Human_RBP_ID_18603938,Human_RBP_ID_22035798,Human_RBP_ID_22159027,Human_RBP_ID_22571966,Human_RBP_ID_27198598,Human_RBP_ID_27409492 89146 RMVar_ID_89146 Human_SNP_ID_483750701 m1A Human chr11 + 119094671 119094671 119094671 GGCTCGGGTCTTCCGCGCCACGGAGGTCCCCGAAGAGCGCCCAAGCCGCATCCGGAAGGCCCGAA GGCTCGGGTCTTCCGCGCCACGGAGGTCCCCGTAGAGCGCCCAAGCCGCATCCGGAAGGCCCGAA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:119094276..119095050 26863410 MeRIP-seq:(Medium) rs1243905016 Functional Loss SNV dbSNP153 33..33 33 - - - 89147 RMVar_ID_89147 Human_SNP_ID_483750702 m1A Human chr11 + 119094674 119094674 119094674 TCGGGTCTTCCGCGCCACGGAGGTCCCCGAAGAGCGCCCAAGCCGCATCCGGAAGGCCCGAACCC TCGGGTCTTCCGCGCCACGGAGGTCCCCGAAGGGCGCCCAAGCCGCATCCGGAAGGCCCGAACCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:119094651..119094675 26863196 MeRIP-seq:(Medium) rs1184120819 Functional Loss SNV dbSNP153 33..33 33 - - - 89148 RMVar_ID_89148 Human_SNP_ID_483750745 m1A Human chr11 + 119094827 119094784 119094827 GGCCGGGCGGCGAAGGCGGGCGAGGGGAGGGGAGGGGAAGGGAGCCGCGGCCCGCTTGCCCCGCA _________________________________GGGGAAGGGAGCCGCGGCCCGCTTGCCCCGCA CGGGGACTCGAGGCCGGGCGGCGAAGGCGGGCGAGGGGAGGGGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119094776..119095005 26863196 MeRIP-seq:(Medium) rs1406282036 Functional Loss DEL dbSNP153 1..33 33 - - - 89149 RMVar_ID_89149 Human_SNP_ID_483750780 m1A Human chr11 - 119094877 119094877 119094877 CTTTTAAGGGCCACCACCGCCCTCATGGAAAGAGCTGAGCCGCTTCAGACTGCGGGGCAAGCGGG CTTTTAAGGGCCACCACCGCCCTCATGGAAAGTGCTGAGCCGCTTCAGACTGCGGGGCAAGCGGG T A H2AX Ensembl:ENSG00000188486 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:119094826..119094939 26863196 MeRIP-seq:(Medium) rs1186592905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_274859,Human_RBP_ID_390295,Human_RBP_ID_1776199,Human_RBP_ID_8345514,Human_RBP_ID_8767348,Human_RBP_ID_17231173,Human_RBP_ID_17347627,Human_RBP_ID_22705599 89150 RMVar_ID_89150 Human_SNP_ID_483752827 m1A Human chr11 + 119101759 119101759 119101759 TCAGCAGTATGGAGTGGCCGCTCCCCACAGGCAGGCTCTTCCCACACCAATCTGAGCAAAACCCA TCAGCAGTATGGAGTGGCCGCTCCCCACAGGCGGGCTCTTCCCACACCAATCTGAGCAAAACCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:119101709..119101851 26863196 MeRIP-seq:(Medium) rs376584369 Functional Loss SNV dbSNP153 33..33 33 - - - 89151 RMVar_ID_89151 Human_SNP_ID_483757884 m1A Human chr11 - 119121625 119121625 119121625 GCACATACCCCAGCTTACCGTCTGTCGGCTCCAGGTCTCTTCAGCTCTTCTCCCACCTCAGACCA GCACATACCCCAGCTTACCGTCTGTCGGCTCCGGGTCTCTTCAGCTCTTCTCCCACCTCAGACCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119121615..119121681 26863196 MeRIP-seq:(Medium) rs1409955537 Functional Loss SNV dbSNP153 33..33 33 - - - 89152 RMVar_ID_89152 Human_SNP_ID_483773559 m1A Human chr11 + 119179819 119179819 119179819 ACAACGATGATGTTCTGGACCAGATGGGCGCCAGTATCCTGGGCGTGGAGGGCCCCCGGCGCCAC ACAACGATGATGTTCTGGACCAGATGGGCGCCGGTATCCTGGGCGTGGAGGGCCCCCGGCGCCAC A G NLRX1 Ensembl:ENSG00000160703 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119179769..119179840 26863196 MeRIP-seq:(Medium) rs748313124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322241,RMVar_hsa_circ_153509 89153 RMVar_ID_89153 Human_SNP_ID_483773625 m1A Human chr11 + 119179957 119179957 119179957 ACCGAGCTGTGCTAGCTCAGCTTGGCTGCCCCATCAAGAACCTGGATGCCCTGGAGAATGCCCAG ACCGAGCTGTGCTAGCTCAGCTTGGCTGCCCCTTCAAGAACCTGGATGCCCTGGAGAATGCCCAG A T NLRX1 Ensembl:ENSG00000160703 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119179908..119180008 32194978 MeRIP-seq:(Medium) rs1169307117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322241,RMVar_hsa_circ_153509 89154 RMVar_ID_89154 Human_SNP_ID_483777064 m1A Human chr11 - 119190341 119190341 119190341 GGCACAAGGAGCAGCAACGCCAGTTTGGACTCACCCCCCCTGGATCTTTGAGGCCACCAGCCCCT GGCACAAGGAGCAGCAACGCCAGTTTGGACTCTCCCCCCCTGGATCTTTGAGGCCACCAGCCCCT T A CCDC153 Ensembl:ENSG00000248712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119190290..119190444 26863196 MeRIP-seq:(Medium) rs749151879 Functional Loss SNV dbSNP153 33..33 33 - - - 89155 RMVar_ID_89155 Human_SNP_ID_483777065 m1A Human chr11 - 119190341 119190341 119190341 GGCACAAGGAGCAGCAACGCCAGTTTGGACTCACCCCCCCTGGATCTTTGAGGCCACCAGCCCCT GGCACAAGGAGCAGCAACGCCAGTTTGGACTCGCCCCCCCTGGATCTTTGAGGCCACCAGCCCCT T C CCDC153 Ensembl:ENSG00000248712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119190290..119190444 26863196 MeRIP-seq:(Medium) rs749151879 Functional Loss SNV dbSNP153 33..33 33 - - - 89156 RMVar_ID_89156 Human_SNP_ID_483777066 m1A Human chr11 - 119190341 119190341 119190341 GGCACAAGGAGCAGCAACGCCAGTTTGGACTCACCCCCCCTGGATCTTTGAGGCCACCAGCCCCT GGCACAAGGAGCAGCAACGCCAGTTTGGACTCCCCCCCCCTGGATCTTTGAGGCCACCAGCCCCT T G CCDC153 Ensembl:ENSG00000248712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119190290..119190444 26863196 MeRIP-seq:(Medium) rs749151879 Functional Loss SNV dbSNP153 33..33 33 - - - 89157 RMVar_ID_89157 Human_SNP_ID_483778676 m1A Human chr11 + 119195931 119195931 119195931 GGCCTGGGTCCTGGGAGCCAATCCTTGGTGGCAAATTTCTCTTGAGGGCAGGACTGAGGGCTGGA GGCCTGGGTCCTGGGAGCCAATCCTTGGTGGCGAATTTCTCTTGAGGGCAGGACTGAGGGCTGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119195929..119195994 26863196 MeRIP-seq:(Medium) rs1039295835 Functional Loss SNV dbSNP153 33..33 33 - - - 89158 RMVar_ID_89158 Human_SNP_ID_483781599 m1A Human chr11 - 119206894 119206893 119206895 CCCTCATTGTACTTCCGCCCCACTGACTTCCCAGTTAACCTTCGCCCCAGCCCCCACTCCATCTT CCCTCATTGTACTTCCGCCCCACTGACTTCC__GTTAACCTTCGCCCCAGCCCCCACTCCATCTT CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119206843..119207043 26863196 MeRIP-seq:(Medium) rs1202453831 Functional Loss DEL dbSNP153 32..33 33 - - - 89159 RMVar_ID_89159 Human_SNP_ID_483808440 m1A Human chr11 - 119308628 119308624 119308629 TGCATACATATGTGTGTATATATGGTTTTGTCAGGTGTGTAAATTTGCAAATTGTTTCCTTTATA TGCATACATATGTGTGTATATATGGTTTTGT_____GTGTAAATTTGCAAATTGTTTCCTTTATA CACCTG C MCAM Ensembl:ENSG00000076706 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:119308578..119308778 32194978 MeRIP-seq:(Medium) rs1194471110 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_390445,Human_RBP_ID_1454645,Human_RBP_ID_1776223,Human_RBP_ID_2253380,Human_RBP_ID_8345585,Human_RBP_ID_21883232,Human_RBP_ID_23490014,Human_RBP_ID_26409079,Human_RBP_ID_27409567 89160 RMVar_ID_89160 Human_SNP_ID_483808816 m1A Human chr11 - 119309475 119309475 119309475 AGGCTGGCTTCCACCATCCAGGTGCACCACTGAAGTGAGGACACACCGGAGCCAGGCGCCTGCTC AGGCTGGCTTCCACCATCCAGGTGCACCACTGGAGTGAGGACACACCGGAGCCAGGCGCCTGCTC T C MCAM Ensembl:ENSG00000076706 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119309424..119309525 32194978 MeRIP-seq:(Medium) rs951304608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26804177,Human_RBP_ID_27409586 Human_Splice_Rec_1308440 89161 RMVar_ID_89161 Human_SNP_ID_483808861 m1A Human chr11 + 119309621 119309621 119309621 AAGAAAAAACACGTTCTGCAAGAAACTCTCCTACCCGCTCGGGAGACTGGGGCTCCTTGCTTGGG AAGAAAAAACACGTTCTGCAAGAAACTCTCCTGCCCGCTCGGGAGACTGGGGCTCCTTGCTTGGG A G CBL Ensembl:ENSG00000110395 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:119309574..119309675 32194978 MeRIP-seq:(Medium) rs1294387027 Functional Loss SNV dbSNP153 33..33 33 - - - 89162 RMVar_ID_89162 Human_SNP_ID_483809166 m1A Human chr11 - 119310423 119310421 119310423 CGTCTCGTAAGAGCGAACTTGTAGTTGAAGTTAAGTCAGATAAGCTCCCAGAAGAGATGGGCCTC CGTCTCGTAAGAGCGAACTTGTAGTTGAAGTT__GTCAGATAAGCTCCCAGAAGAGATGGGCCTC CTT C MCAM Ensembl:ENSG00000076706 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119310325..119310474 26863196 MeRIP-seq:(Medium) rs762592393 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1308382,Human_Splice_Rec_1308383,Human_Splice_Rec_1308408,Human_Splice_Rec_1308409,Human_Splice_Rec_1308436,Human_Splice_Rec_1308437,Human_Splice_Rec_1308450,Human_Splice_Rec_1308451 Human_miRNA_ID_2205318,Human_miRNA_ID_2929053 RMVar_hsa_circ_113856,RMVar_hsa_circ_153540 89163 RMVar_ID_89163 Human_SNP_ID_483809320 m1A Human chr11 + 119310834 119310834 119310834 AGAGGAAATAGAGGACAGCGCCCAGCACCGCCAGGACCAGGATGCACACAATCACAGCCACGATG AGAGGAAATAGAGGACAGCGCCCAGCACCGCCGGGACCAGGATGCACACAATCACAGCCACGATG A G CBL Ensembl:ENSG00000110395 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119310785..119310886 32194978 MeRIP-seq:(Medium) rs138745100 Functional Loss SNV dbSNP153 33..33 33 - - - 89164 RMVar_ID_89164 Human_SNP_ID_483809470 m1A Human chr11 - 119311150 119311150 119311150 ATTTAACCACCCTCACACCAGACTCCAACACAACCACTGGCCTCAGCACTTCCACTGCCAGTCCT ATTTAACCACCCTCACACCAGACTCCAACACAGCCACTGGCCTCAGCACTTCCACTGCCAGTCCT T C MCAM Ensembl:ENSG00000076706 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119311099..119311192 26863196 MeRIP-seq:(Medium) rs771280059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748987,Human_RBP_ID_869800,Human_RBP_ID_4150816,Human_RBP_ID_27409609 Human_Splice_Rec_1308378,Human_Splice_Rec_1308379,Human_Splice_Rec_1308434,Human_Splice_Rec_1308441,Human_Splice_Rec_1308446,Human_Splice_Rec_1308447 Human_miRNA_ID_1109821,Human_miRNA_ID_1598179,Human_miRNA_ID_1620022,Human_miRNA_ID_2057911,Human_miRNA_ID_2316015,Human_miRNA_ID_2319169,Human_miRNA_ID_2322329,Human_miRNA_ID_2325496,Human_miRNA_ID_2519872,Human_miRNA_ID_2523038,Human_miRNA_ID_2774859,Human_miRNA_ID_2822233,Human_miRNA_ID_2828363,Human_miRNA_ID_2831520,Human_miRNA_ID_2835639,Human_miRNA_ID_2840995 RMVar_hsa_circ_98748,RMVar_hsa_circ_116554,RMVar_hsa_circ_113856,RMVar_hsa_circ_153540,RMVar_hsa_circ_106268,RMVar_hsa_circ_153541,RMVar_hsa_circ_153543,RMVar_hsa_circ_82682,RMVar_hsa_circ_153544,RMVar_hsa_circ_153542 89165 RMVar_ID_89165 Human_SNP_ID_483809557 m1A Human chr11 + 119311378 119311378 119311378 TCTCCAACAGCTCCGGGGTCACGAGGACATTCAGGGTGCTCAGGACTCGCTGTGGATCTTGGTCT TCTCCAACAGCTCCGGGGTCACGAGGACATTCCGGGTGCTCAGGACTCGCTGTGGATCTTGGTCT A C CBL Ensembl:ENSG00000110395 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119311233..119311541 32194978 MeRIP-seq:(Medium) rs1395242865 Functional Loss SNV dbSNP153 33..33 33 - - - 89166 RMVar_ID_89166 Human_SNP_ID_483809581 m1A Human chr11 - 119311423 119311423 119311423 CATCCCCTGAGCTGCCTCCTTCCTTTCCTCGCAGGCAAGTGAACAAGACCAAGATCCACAGCGAG CATCCCCTGAGCTGCCTCCTTCCTTTCCTCGCCGGCAAGTGAACAAGACCAAGATCCACAGCGAG T G MCAM Ensembl:ENSG00000076706 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr11:119311305..119311447;chr11:119311376..119311650 26863196 MeRIP-seq:(Medium) rs111323193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98748,RMVar_hsa_circ_116554,RMVar_hsa_circ_113856,RMVar_hsa_circ_153540,RMVar_hsa_circ_153541,RMVar_hsa_circ_122983,RMVar_hsa_circ_153543,RMVar_hsa_circ_82682,RMVar_hsa_circ_153544,RMVar_hsa_circ_153546,RMVar_hsa_circ_106467,RMVar_hsa_circ_153545 89167 RMVar_ID_89167 Human_SNP_ID_483810085 m1A Human chr11 + 119312627 119312627 119312627 CTTCCTTCAGCATTCCCACGGGCTCCACTTCCAGCCACACTTTTTCTGTCGGGTCTGCATAGGCA CTTCCTTCAGCATTCCCACGGGCTCCACTTCCGGCCACACTTTTTCTGTCGGGTCTGCATAGGCA A G CBL Ensembl:ENSG00000110395 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119312097..119312640 32194978 MeRIP-seq:(Medium) rs1460356462 Functional Loss SNV dbSNP153 33..33 33 - - - 89168 RMVar_ID_89168 Human_SNP_ID_483810814 m1A Human chr11 + 119314936 119314936 119314936 TCTTGGGGGGTGACTTGAGTCAGGGCCAGAGTAGCCCCTCTGTCCTGGAGGCTGAGCCGCTGCTC TCTTGGGGGGTGACTTGAGTCAGGGCCAGAGTGGCCCCTCTGTCCTGGAGGCTGAGCCGCTGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119314804..119314941 26863196 MeRIP-seq:(Medium) rs1025292376 Functional Loss SNV dbSNP153 33..33 33 - - - 89169 RMVar_ID_89169 Human_SNP_ID_483810839 m1A Human chr11 - 119314986 119314986 119314986 TCATCTTCCGTGTGCGCCAGGGCCAGGGCCAGAGCGAACCTGGGGAGTACGAGCAGCGGCTCAGC TCATCTTCCGTGTGCGCCAGGGCCAGGGCCAGGGCGAACCTGGGGAGTACGAGCAGCGGCTCAGC T C MCAM Ensembl:ENSG00000076706 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119314741..119315074 32194978 MeRIP-seq:(Medium) rs1167165627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226251,Human_RBP_ID_22755119 Human_Splice_Rec_1308358,Human_Splice_Rec_1308388,Human_Splice_Rec_1308416,Human_Splice_Rec_1308454,Human_Splice_Rec_1308464,Human_Splice_Rec_1308472,Human_Splice_Rec_1308480,Human_Splice_Rec_1308488,Human_Splice_Rec_1308494,Human_Splice_Rec_1308502,Human_Splice_Rec_1308514,Human_Splice_Rec_1308520,Human_Splice_Rec_1308526,Human_Splice_Rec_1308530 Human_miRNA_ID_2257609 RMVar_hsa_circ_113856,RMVar_hsa_circ_153540,RMVar_hsa_circ_153546,RMVar_hsa_circ_106467,RMVar_hsa_circ_105152,RMVar_hsa_circ_153548 89170 RMVar_ID_89170 Human_SNP_ID_483815703 m1A Human chr11 + 119334614 119334614 119334614 TGGCTGCCTCTCCCACTCCCCTTTTGGGTGCAAAGCGCCGCTAGCGGGAAGACGGGGGCCGGGCG TGGCTGCCTCTCCCACTCCCCTTTTGGGTGCAGAGCGCCGCTAGCGGGAAGACGGGGGCCGGGCG A G RNF26 Ensembl:ENSG00000173456 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119334568..119334861 26863196 MeRIP-seq:(Medium) rs985265211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4150862,Human_RBP_ID_5235349,Human_RBP_ID_5314474,Human_RBP_ID_5436093,Human_RBP_ID_5460014,Human_RBP_ID_5521036,Human_RBP_ID_9321808,Human_RBP_ID_27198709 89171 RMVar_ID_89171 Human_SNP_ID_483815806 m1A Human chr11 - 119335025 119335025 119335025 TCAATATTTTAGGGGGTCTGGGATTAATTTGGAAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA TCAATATTTTAGGGGGTCTGGGATTAATTTGGTAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119334976..119335085 26863196 MeRIP-seq:(Medium) rs12797083 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11580,GWAS_ID_11581,GWAS_ID_11582,GWAS_ID_11583,GWAS_ID_11584,GWAS_ID_11585,GWAS_ID_11586,GWAS_ID_11587,GWAS_ID_11588 89172 RMVar_ID_89172 Human_SNP_ID_483815807 m1A Human chr11 - 119335025 119335025 119335025 TCAATATTTTAGGGGGTCTGGGATTAATTTGGAAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA TCAATATTTTAGGGGGTCTGGGATTAATTTGGGAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119334976..119335085 26863196 MeRIP-seq:(Medium) rs12797083 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11580,GWAS_ID_11581,GWAS_ID_11582,GWAS_ID_11583,GWAS_ID_11584,GWAS_ID_11585,GWAS_ID_11586,GWAS_ID_11587,GWAS_ID_11588 89173 RMVar_ID_89173 Human_SNP_ID_483815808 m1A Human chr11 - 119335025 119335025 119335025 TCAATATTTTAGGGGGTCTGGGATTAATTTGGAAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA TCAATATTTTAGGGGGTCTGGGATTAATTTGGCAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119334976..119335085 26863196 MeRIP-seq:(Medium) rs12797083 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11580,GWAS_ID_11581,GWAS_ID_11582,GWAS_ID_11583,GWAS_ID_11584,GWAS_ID_11585,GWAS_ID_11586,GWAS_ID_11587,GWAS_ID_11588 89174 RMVar_ID_89174 Human_SNP_ID_483828960 m1A Human chr11 + 119381567 119381552 119381567 CCGGCTGGCGCTGGCGCGGCGCAGTGAGCACCAGCTGACGAAGAGGGCTCCCCGGCCTCGGCTCC CCGGCTGGCGCTGGCGCG_______________GCTGACGAAGAGGGCTCCCCGGCCTCGGCTCC GGCGCAGTGAGCACCA G USP2-AS1,AP003396.3 Ensembl:ENSG00000245248,Ensembl:ENSG00000254740 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119381490..119381596 26863196 MeRIP-seq:(Medium) rs1450645268 Functional Loss DEL dbSNP153 19..33 33 - - - 89175 RMVar_ID_89175 Human_SNP_ID_483828967 m1A Human chr11 + 119381567 119381560 119381567 CCGGCTGGCGCTGGCGCGGCGCAGTGAGCACCAGCTGACGAAGAGGGCTCCCCGGCCTCGGCTCC CCGGCTGGCGCTGGCGCGGCGCAGTG_______GCTGACGAAGAGGGCTCCCCGGCCTCGGCTCC GAGCACCA G USP2-AS1,AP003396.3 Ensembl:ENSG00000245248,Ensembl:ENSG00000254740 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119381490..119381596 26863196 MeRIP-seq:(Medium) rs1313326128 Functional Loss DEL dbSNP153 27..33 33 - - - 89176 RMVar_ID_89176 Human_SNP_ID_483832111 m1A Human chr11 + 119395030 119395030 119395030 TACTTCAAAATTGCCGTGCTCTACCTCTCCCCAGTGCACAAAAACACTCTCCACACCAAGCTGCT TACTTCAAAATTGCCGTGCTCTACCTCTCCCCGGTGCACAAAAACACTCTCCACACCAAGCTGCT A G USP2-AS1 Ensembl:ENSG00000245248 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119394920..119395094 26863196 MeRIP-seq:(Medium) rs757411402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8246950 Human_Splice_Rec_1308710,Human_Splice_Rec_1308714,Human_Splice_Rec_1308718,Human_Splice_Rec_1308724,Human_Splice_Rec_1308730,Human_Splice_Rec_1308734,Human_Splice_Rec_1308740,Human_Splice_Rec_1308744,Human_Splice_Rec_1308748,Human_Splice_Rec_1308752,Human_Splice_Rec_1308772,Human_Splice_Rec_1308778 RMVar_hsa_circ_16755,RMVar_hsa_circ_105289,RMVar_hsa_circ_153558 89177 RMVar_ID_89177 Human_SNP_ID_483837597 m1A Human chr11 + 119419412 119419412 119419412 TTCCTGTCTCCTCCATGGGCCCCACCAGTCACAGGGACATGAAATCCGTGGCCTGGAGGAGGGAG TTCCTGTCTCCTCCATGGGCCCCACCAGTCACCGGGACATGAAATCCGTGGCCTGGAGGAGGGAG A C USP2-AS1 Ensembl:ENSG00000245248 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119419269..119419519 32194978 MeRIP-seq:(Medium) rs750464352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16755 89178 RMVar_ID_89178 Human_SNP_ID_483849162 m1A Human chr11 + 119469943 119469943 119469943 AGAGGCAGAGAGATCCAAGCGCACAGAAAAACACAAGAAGATTCAGCCCTGTCATCTTGTGCAAA AGAGGCAGAGAGATCCAAGCGCACAGAAAAACCCAAGAAGATTCAGCCCTGTCATCTTGTGCAAA A C USP2-AS1 Ensembl:ENSG00000245248 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119469788..119475397 26863196 MeRIP-seq:(Medium) rs756265276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868905 Human_Splice_Rec_1308727,Human_Splice_Rec_1308775,Human_Splice_Rec_1308781 RMVar_hsa_circ_16755 89179 RMVar_ID_89179 Human_SNP_ID_483849163 m1A Human chr11 + 119469943 119469943 119469943 AGAGGCAGAGAGATCCAAGCGCACAGAAAAACACAAGAAGATTCAGCCCTGTCATCTTGTGCAAA AGAGGCAGAGAGATCCAAGCGCACAGAAAAACTCAAGAAGATTCAGCCCTGTCATCTTGTGCAAA A T USP2-AS1 Ensembl:ENSG00000245248 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119469788..119475397 26863196 MeRIP-seq:(Medium) rs756265276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_868905 Human_Splice_Rec_1308727,Human_Splice_Rec_1308775,Human_Splice_Rec_1308781 RMVar_hsa_circ_16755 89180 RMVar_ID_89180 Human_SNP_ID_483849169 m1A Human chr11 - 119469962 119469962 119469962 TGAATTATGTGGAACTCACTTTGCACAAGATGACAGGGCTGAATCTTCTTGTGTTTTTCTGTGCG TGAATTATGTGGAACTCACTTTGCACAAGATGGCAGGGCTGAATCTTCTTGTGTTTTTCTGTGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119469912..119475397 26863196 MeRIP-seq:(Medium) rs1036827492 Functional Loss SNV dbSNP153 33..33 33 - - - 89181 RMVar_ID_89181 Human_SNP_ID_483897467 m1A Human chr11 - 119665022 119665019 119665022 TGCAGTACCCCGACGACTCAGACGACGAGAAGAAGGCCGGCCCACTGGGTGGAAGCAGCTATGAG TGCAGTACCCCGACGACTCAGACGACGAGAAG___GCCGGCCCACTGGGTGGAAGCAGCTATGAG CCTT C NECTIN1 Ensembl:ENSG00000110400 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:119664999..119665132 26863196 MeRIP-seq:(Medium) rs1022251180 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_153562 89182 RMVar_ID_89182 Human_SNP_ID_483912996 m1A Human chr11 - 119728704 119728702 119728704 GGGCCCGGACTGCGGCCGCGCGGATCCCACCCAGCCCACCCCGCCCCGGCCGACGGCTGCAGCTG GGGCCCGGACTGCGGCCGCGCGGATCCCACCC__CCCACCCCGCCCCGGCCGACGGCTGCAGCTG GCT G NECTIN1 Ensembl:ENSG00000110400 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:119728698..119728824 26863196 MeRIP-seq:(Medium) rs1321893034 Functional Loss DEL dbSNP153 33..34 33 - - - 89183 RMVar_ID_89183 Human_SNP_ID_483912998 m1A Human chr11 - 119728704 119728704 119728704 GGGCCCGGACTGCGGCCGCGCGGATCCCACCCAGCCCACCCCGCCCCGGCCGACGGCTGCAGCTG GGGCCCGGACTGCGGCCGCGCGGATCCCACCCGGCCCACCCCGCCCCGGCCGACGGCTGCAGCTG T C NECTIN1 Ensembl:ENSG00000110400 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:119728698..119728824 26863196 MeRIP-seq:(Medium) rs900655328 Functional Loss SNV dbSNP153 33..33 33 - - - 89184 RMVar_ID_89184 Human_SNP_ID_483912999 m1A Human chr11 - 119728704 119728704 119728704 GGGCCCGGACTGCGGCCGCGCGGATCCCACCCAGCCCACCCCGCCCCGGCCGACGGCTGCAGCTG GGGCCCGGACTGCGGCCGCGCGGATCCCACCCCGCCCACCCCGCCCCGGCCGACGGCTGCAGCTG T G NECTIN1 Ensembl:ENSG00000110400 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:119728698..119728824 26863196 MeRIP-seq:(Medium) rs900655328 Functional Loss SNV dbSNP153 33..33 33 - - - 89185 RMVar_ID_89185 Human_SNP_ID_483913164 m1A Human chr11 - 119729181 119729181 119729181 CGGCGAGTGAGAGAAAGAGAGCGAGAGCAGCGAGCGCGGCTCCACATTGTTGCGGATCGCCGGCA CGGCGAGTGAGAGAAAGAGAGCGAGAGCAGCGGGCGCGGCTCCACATTGTTGCGGATCGCCGGCA T C NECTIN1 Ensembl:ENSG00000110400 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119728738..119729205 26863196 MeRIP-seq:(Medium) rs1385719782 Functional Loss SNV dbSNP153 33..33 33 - - - 89186 RMVar_ID_89186 Human_SNP_ID_279299230 m1A Human chr6 - 61574218 61574218 61574218 GTCACTGGGCAGGCGGTGCCTCTAATACTGGTAATGCTAGAGGTGATGTTTTTGGTAAACAGGCG GTCACTGGGCAGGCGGTGCCTCTAATACTGGTGATGCTAGAGGTGATGTTTTTGGTAAACAGGCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:61574123..61574370 26863410 MeRIP-seq:(Medium) rs62424615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32927,RMVar_hsa_circ_346489,RMVar_hsa_circ_26123 89187 RMVar_ID_89187 Human_SNP_ID_279299270 m1A Human chr6 - 61574304 61574304 61574304 TCGAGCCATTCATACAAGTCCCTATTTAAGGAACAAGTGATCATGCTACCTTTGCACGGTTAGGG TCGAGCCATTCATACAAGTCCCTATTTAAGGATCAAGTGATCATGCTACCTTTGCACGGTTAGGG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:61574182..61574356 26863410 MeRIP-seq:(Medium) rs1281817532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32927,RMVar_hsa_circ_346489,RMVar_hsa_circ_26123 89188 RMVar_ID_89188 Human_SNP_ID_279299396 m1A Human chr6 + 61574525 61574524 61574526 ATTAAAAATTTCGGCTGGGGCGACCTCGGAGTATAACCCAACCTCCGAGCAACATATGCTGAGAC ATTAAAAATTTCGGCTGGGGCGACCTCGGAGCAGAACCCAACCTCCGAGCAACATATGCTGAGAC TAT CAG - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:61574476..61574605 26863196 MeRIP-seq:(Medium) rs796998664 Functional Loss MNV dbSNP153 32..34 33 - - - 89189 RMVar_ID_89189 Human_SNP_ID_279299397 m1A Human chr6 + 61574525 61574525 61574525 ATTAAAAATTTCGGCTGGGGCGACCTCGGAGTATAACCCAACCTCCGAGCAACATATGCTGAGAC ATTAAAAATTTCGGCTGGGGCGACCTCGGAGTGTAACCCAACCTCCGAGCAACATATGCTGAGAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:61574476..61574605 26863196 MeRIP-seq:(Medium) rs1385786254 Functional Loss SNV dbSNP153 33..33 33 - - - 89190 RMVar_ID_89190 Human_SNP_ID_279797740 m1A Human chr6 - 63327792 63327792 63327792 CAAGAAGGAAAGAGAGAAAGAGAAAGAGAAAGAGACAGAGAGAGGAAAAGATAAAGGAGAAGTTG CAAGAAGGAAAGAGAGAAAGAGAAAGAGAAAGGGACAGAGAGAGGAAAAGATAAAGGAGAAGTTG T C RF00017-1287 RNACentral:URS000098E119 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:63327765..63327830 26863196 MeRIP-seq:(Medium) rs1434053868 Functional Loss SNV dbSNP153 33..33 33 - - - 89191 RMVar_ID_89191 Human_SNP_ID_279854310 m1A Human chr6 + 63542798 63542798 63542798 CCACACTTCTTCACAAATCCTACATCCTTTCCATTGCTCTATATGCAAAATACATCCCATATTAT CCACACTTCTTCACAAATCCTACATCCTTTCCGTTGCTCTATATGCAAAATACATCCCATATTAT A G PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63542749..63543000 26863196 MeRIP-seq:(Medium) rs1305678174 Functional Loss SNV dbSNP153 33..33 33 - - - 89192 RMVar_ID_89192 Human_SNP_ID_279854311 m1A Human chr6 + 63542798 63542798 63542798 CCACACTTCTTCACAAATCCTACATCCTTTCCATTGCTCTATATGCAAAATACATCCCATATTAT CCACACTTCTTCACAAATCCTACATCCTTTCCTTTGCTCTATATGCAAAATACATCCCATATTAT A T PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63542749..63543000 26863196 MeRIP-seq:(Medium) rs1305678174 Functional Loss SNV dbSNP153 33..33 33 - - - 89193 RMVar_ID_89193 Human_SNP_ID_279855629 m1A Human chr6 + 63548058 63548058 63548058 GATTCCCTGTTTCTTTTCTGCCCACATCCCCCATATTCCAAAACCCACTACTCATCCACAACTCA GATTCCCTGTTTCTTTTCTGCCCACATCCCCCGTATTCCAAAACCCACTACTCATCCACAACTCA A G PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:63548037..63548135 26863196 MeRIP-seq:(Medium) rs552823432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17090965 89194 RMVar_ID_89194 Human_SNP_ID_279858206 m1A Human chr6 - 63558362 63558362 63558362 GCAGTGGCTCAGAGATTGTCCCCCTCCTTCTAATTTTTTACTGTCAAAAGCCTTATTTGTTCATT GCAGTGGCTCAGAGATTGTCCCCCTCCTTCTAGTTTTTTACTGTCAAAAGCCTTATTTGTTCATT T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63558318..63558435 26863196 MeRIP-seq:(Medium) rs1029578841 Functional Loss SNV dbSNP153 33..33 33 - - - 89195 RMVar_ID_89195 Human_SNP_ID_279861288 m1A Human chr6 - 63572119 63572119 63572119 ATTAAAACGGTCCAGGAGTGCACACATGTCACATGAGGAGACTCGAAGTTTGCCTGAATCGTAAA ATTAAAACGGTCCAGGAGTGCACACATGTCACGTGAGGAGACTCGAAGTTTGCCTGAATCGTAAA T C AL135905.1 Ensembl:ENSG00000266680 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:63572068..63572417 26863196 MeRIP-seq:(Medium) rs762017628 Functional Loss SNV dbSNP153 33..33 33 - - - 89196 RMVar_ID_89196 Human_SNP_ID_279861516 m1A Human chr6 + 63572613 63572593 63572613 GCCTGCATCGCCGCCACCGCCGCTCCGCCACGACCACCGCCGCCTCCTGCCCTGCAGCCACCGCC GCCTGCATCGCCG____________________CCACCGCCGCCTCCTGCCCTGCAGCCACCGCC GCCACCGCCGCTCCGCCACGA G PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:63572476..63573350;chr6:63572501..63573247;chr6:63572521..63572659;chr6:63572074..63572791;chr6:63572451..63572797;chr6:63572476..63572800 26863196,26863410,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1212675221 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_81406,Human_RBP_ID_252038,Human_RBP_ID_666902,Human_RBP_ID_4904112,Human_RBP_ID_7621562,Human_RBP_ID_9336216,Human_RBP_ID_18868460,Human_RBP_ID_22534116,Human_RBP_ID_24168795,Human_RBP_ID_26537455,Human_RBP_ID_27100102 89197 RMVar_ID_89197 Human_SNP_ID_279861531 m1A Human chr6 + 63572616 63572616 63572616 TGCATCGCCGCCACCGCCGCTCCGCCACGACCACCGCCGCCTCCTGCCCTGCAGCCACCGCCACC TGCATCGCCGCCACCGCCGCTCCGCCACGACCGCCGCCGCCTCCTGCCCTGCAGCCACCGCCACC A G PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:63572501..63573397 26863196 MeRIP-seq:(Medium) rs1440554161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81406,Human_RBP_ID_252038,Human_RBP_ID_666902,Human_RBP_ID_4895550,Human_RBP_ID_7621562,Human_RBP_ID_8270225,Human_RBP_ID_9336216,Human_RBP_ID_22534116,Human_RBP_ID_24168795 89198 RMVar_ID_89198 Human_SNP_ID_279861537 m1A Human chr6 + 63572646 63572646 63572646 CCACCGCCGCCTCCTGCCCTGCAGCCACCGCCACCGCCTGTGTCGCCGCCGCCTCGGGACCGGCT CCACCGCCGCCTCCTGCCCTGCAGCCACCGCCCCCGCCTGTGTCGCCGCCGCCTCGGGACCGGCT A C PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:63572114..63573326 26863196 MeRIP-seq:(Medium) rs201190738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_666902,Human_RBP_ID_791977,Human_RBP_ID_4895551,Human_RBP_ID_7621563,Human_RBP_ID_8270225,Human_RBP_ID_9336216,Human_RBP_ID_15863359,Human_RBP_ID_22534116,Human_RBP_ID_24168795,Human_RBP_ID_27100104 Human_Splice_Rec_782167 89199 RMVar_ID_89199 Human_SNP_ID_279861543 m1A Human chr6 - 63572667 63572667 63572667 AAGATTGTGGCCTAATCATACAGCCGGTCCCGAGGCGGCGGCGACACAGGCGGTGGCGGTGGCTG AAGATTGTGGCCTAATCATACAGCCGGTCCCGGGGCGGCGGCGACACAGGCGGTGGCGGTGGCTG T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:63572401..63573514 26863196 MeRIP-seq:(Medium) rs1440326209 Functional Loss SNV dbSNP153 33..33 33 - - - 89200 RMVar_ID_89200 Human_SNP_ID_279862645 m1A Human chr6 - 63576408 63576405 63576409 AATTGCTGTTTAAAAGAAAAAGACAGAAAGAGAGAATAAGTTATTTTCCAATTCAAAAGAAATAC AATTGCTGTTTAAAAGAAAAAGACAGAAAGA____ATAAGTTATTTTCCAATTCAAAAGAAATAC TTCTC T RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63576406..63576627 26863196 MeRIP-seq:(Medium) rs952747250 Functional Loss DEL dbSNP153 32..35 33 - - - 89201 RMVar_ID_89201 Human_SNP_ID_279862646 m1A Human chr6 - 63576408 63576405 63576409 AATTGCTGTTTAAAAGAAAAAGACAGAAAGAGAGAATAAGTTATTTTCCAATTCAAAAGAAATAC AATTGCTGTTTAAAAGAAAAAGACAGAAAGA__GAATAAGTTATTTTCCAATTCAAAAGAAATAC TTCTC TTC RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63576406..63576627 26863196 MeRIP-seq:(Medium) rs952747250 Functional Loss DEL dbSNP153 32..33 33 - - - 89202 RMVar_ID_89202 Human_SNP_ID_279862655 m1A Human chr6 + 63576438 63576438 63576438 TCTCTCTTTCTGTCTTTTTCTTTTAAACAGCAATTCTGTGGTGTTCTTGGTCACACATTTATGGA TCTCTCTTTCTGTCTTTTTCTTTTAAACAGCAGTTCTGTGGTGTTCTTGGTCACACATTTATGGA A G PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:63576426..63576475 26863196 MeRIP-seq:(Medium) rs970501269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81421,Human_RBP_ID_666905,Human_RBP_ID_1218360,Human_RBP_ID_3014548,Human_RBP_ID_3813351,Human_RBP_ID_8647957,Human_RBP_ID_17309034,Human_RBP_ID_22683017,Human_RBP_ID_26038361,Human_RBP_ID_27100107,Human_RBP_ID_27348605 Human_Splice_Rec_782112,Human_Splice_Rec_782126,Human_Splice_Rec_782130,Human_Splice_Rec_782132,Human_Splice_Rec_782142,Human_Splice_Rec_782152,Human_Splice_Rec_782168,Human_Splice_Rec_782178 RMVar_hsa_circ_20854,RMVar_hsa_circ_314933,RMVar_hsa_circ_26972 89203 RMVar_ID_89203 Human_SNP_ID_279862777 m1A Human chr6 + 63576972 63576972 63576972 TATTACACACAATCCAACCAATGCGACCTTAAACAAATTTATAGAGGTAAGATTTGATATGTTTT TATTACACACAATCCAACCAATGCGACCTTAAGCAAATTTATAGAGGTAAGATTTGATATGTTTT A G PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:63576922..63577003 26863196 MeRIP-seq:(Medium) rs779426223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2024707,Human_RBP_ID_7621608,Human_RBP_ID_8902760,Human_RBP_ID_17309041,Human_RBP_ID_19129540 Human_Splice_Rec_782113,Human_Splice_Rec_782133,Human_Splice_Rec_782143,Human_Splice_Rec_782153,Human_Splice_Rec_782161,Human_Splice_Rec_782169,Human_Splice_Rec_782179 RMVar_hsa_circ_20854,RMVar_hsa_circ_314933,RMVar_hsa_circ_26972 89204 RMVar_ID_89204 Human_SNP_ID_279864300 m1A Human chr6 - 63582801 63582799 63582801 TGCCCTAGGGAAAAGAGGGCACTAGGGGAAACAATGGTTGCAGTGCACTGCAGAATGACCAATGG TGCCCTAGGGAAAAGAGGGCACTAGGGGAAAC__TGGTTGCAGTGCACTGCAGAATGACCAATGG ATT A RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:63582751..63582950 26863196 MeRIP-seq:(Medium) rs763634136 Functional Loss DEL dbSNP153 33..34 33 - - - 89205 RMVar_ID_89205 Human_SNP_ID_279864306 m1A Human chr6 - 63582820 63582820 63582820 CGTGGGAATAGGAGAGCAATGCCCTAGGGAAAAGAGGGCACTAGGGGAAACAATGGTTGCAGTGC CGTGGGAATAGGAGAGCAATGCCCTAGGGAAATGAGGGCACTAGGGGAAACAATGGTTGCAGTGC T A RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:63582801..63582825 26863196 MeRIP-seq:(Medium) rs945810969 Functional Loss SNV dbSNP153 33..33 33 - - - 89206 RMVar_ID_89206 Human_SNP_ID_279864319 m1A Human chr6 + 63582860 63582851 63582860 AGGGCATTGCTCTCCTATTCCCACGCCTTAACACAGCTCTATACCTAGAAGCAGCCAGCCCAGGC AGGGCATTGCTCTCCTATTCCCAC_________CAGCTCTATACCTAGAAGCAGCCAGCCCAGGC CGCCTTAACA C PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:63582810..63582902 26863196 MeRIP-seq:(Medium) rs1348429177 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_667021,Human_RBP_ID_1048336,Human_RBP_ID_8216125,Human_RBP_ID_9196288,Human_RBP_ID_15863762,Human_RBP_ID_17307742,Human_RBP_ID_17537935,Human_RBP_ID_26537590,Human_RBP_ID_26828612,Human_RBP_ID_27757637 89207 RMVar_ID_89207 Human_SNP_ID_279893299 m1A Human chr6 - 63697147 63697147 63697147 TTCTGATAAATACCTCCCTCCATGTGGAGTGAATCCCATCCCCTCTTGTCTTCCCGAGTTTCACA TTCTGATAAATACCTCCCTCCATGTGGAGTGACTCCCATCCCCTCTTGTCTTCCCGAGTTTCACA T G lnc-EYS-1 RNACentral:URS0000D5DD7C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:63697128..63697257 26863196 MeRIP-seq:(Medium) rs1041903497 Functional Loss SNV dbSNP153 33..33 33 - - - 89208 RMVar_ID_89208 Human_SNP_ID_279897463 m1A Human chr6 - 63713027 63713027 63713027 GGAAAATTAGGAGGCCCTGGAAATGGAAATCCAGGTGGGCTAGACTTGAGATGCTGAAGGTTGGG GGAAAATTAGGAGGCCCTGGAAATGGAAATCCTGGTGGGCTAGACTTGAGATGCTGAAGGTTGGG T A lnc-EYS-1 RNACentral:URS0000D5DD7C lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:63712976..63713050 26863196 MeRIP-seq:(Medium) rs773329241 Functional Loss SNV dbSNP153 33..33 33 - - - 89209 RMVar_ID_89209 Human_SNP_ID_279897464 m1A Human chr6 - 63713027 63713027 63713027 GGAAAATTAGGAGGCCCTGGAAATGGAAATCCAGGTGGGCTAGACTTGAGATGCTGAAGGTTGGG GGAAAATTAGGAGGCCCTGGAAATGGAAATCCGGGTGGGCTAGACTTGAGATGCTGAAGGTTGGG T C lnc-EYS-1 RNACentral:URS0000D5DD7C lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:63712976..63713050 26863196 MeRIP-seq:(Medium) rs773329241 Functional Loss SNV dbSNP153 33..33 33 - - - 89210 RMVar_ID_89210 Human_SNP_ID_279897638 m1A Human chr6 + 63713457 63713457 63713457 ATAGACGCAGAGACAGAAGCCAAGACAAGGACAGAGACAGAAAAAGCAGGGAGGAAGGGCACAAA ATAGACGCAGAGACAGAAGCCAAGACAAGGACGGAGACAGAAAAAGCAGGGAGGAAGGGCACAAA A G PHF3 Ensembl:ENSG00000118482 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:63713348..63713654;chr6:63713239..63713700;chr6:63713273..63713725 26863196 MeRIP-seq:(Medium) rs981759249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9350248 Human_miRNA_ID_835742,Human_miRNA_ID_1095400 89211 RMVar_ID_89211 Human_SNP_ID_281531672 m1A Human chr6 - 69796845 69796845 69796845 CGACTTCTGGCGCGGCCTCGGCGGAGCTGGTGATCGGCTGGTGCATATTCGGCCTCTTACTACTG CGACTTCTGGCGCGGCCTCGGCGGAGCTGGTGGTCGGCTGGTGCATATTCGGCCTCTTACTACTG T C LMBRD1 Ensembl:ENSG00000168216 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:69796753..69796845 26863196 MeRIP-seq:(Medium) rs139251334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667188,Human_RBP_ID_4904120,Human_RBP_ID_18958520 Human_Splice_Rec_782951,Human_Splice_Rec_783067,Human_Splice_Rec_783099,Human_Splice_Rec_783287,Human_Splice_Rec_783405,Human_Splice_Rec_783437,Human_Splice_Rec_783469,Human_Splice_Rec_783501,Human_Splice_Rec_783561,Human_Splice_Rec_783597,Human_Splice_Rec_783867,Human_Splice_Rec_783922,Human_Splice_Rec_783923 89212 RMVar_ID_89212 Human_SNP_ID_281680805 m1A Human chr6 - 70413568 70413568 70413568 GCCCCCTCACATCGCCATCACAGCAACCGCAAACACCGCAACCGCGGAGCCGGTTCGTCACCGCG GCCCCCTCACATCGCCATCACAGCAACCGCAATCACCGCAACCGCGGAGCCGGTTCGTCACCGCG T A FAM135A-AS1 Ensembl:ENSG00000224349 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:70413328..70413653 26863196 MeRIP-seq:(Medium) rs1423471990 Functional Loss SNV dbSNP153 33..33 33 - - - 89213 RMVar_ID_89213 Human_SNP_ID_281680812 m1A Human chr6 + 70413589 70413589 70413589 CGGTTGCGGTGTTTGCGGTTGCTGTGATGGCGATGTGAGGGGGCCCGGGGCGGGATGGTGCTGAC CGGTTGCGGTGTTTGCGGTTGCTGTGATGGCGTTGTGAGGGGGCCCGGGGCGGGATGGTGCTGAC A T FAM135A Ensembl:ENSG00000082269 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:70413539..70413655 26863196 MeRIP-seq:(Medium) rs964481406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904125,Human_RBP_ID_22106054,Human_RBP_ID_24169908 89214 RMVar_ID_89214 Human_SNP_ID_281718327 m1A Human chr6 + 70567004 70567004 70567004 GCTGGGTCTCGGCCACGGCGTGGAGAGCGGCAAGTAAGCACCTGGCCTCGGGGCCACGGTCGCGG GCTGGGTCTCGGCCACGGCGTGGAGAGCGGCAGGTAAGCACCTGGCCTCGGGGCCACGGTCGCGG A G SDHAF4 Ensembl:ENSG00000154079 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:70566955..70567049 26863196 MeRIP-seq:(Medium) rs780039929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904126,Human_RBP_ID_18425454,Human_RBP_ID_19131491 Human_Splice_Rec_784819,Human_Splice_Rec_784821 89215 RMVar_ID_89215 Human_SNP_ID_281721498 m1A Human chr6 - 70579478 70579478 70579478 GGTAACTTCGGCTTCTTAAGGGACTGTTTGACAAGTTCAGACTTTCCTCCTTGAGAAGAACTTGT GGTAACTTCGGCTTCTTAAGGGACTGTTTGACGAGTTCAGACTTTCCTCCTTGAGAAGAACTTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:70579377..70579479 26863196 MeRIP-seq:(Medium) rs777397413 Functional Loss SNV dbSNP153 33..33 33 - - - 89216 RMVar_ID_89216 Human_SNP_ID_281723743 m1A Human chr6 + 70588936 70588936 70588936 CAGCCTGACCAATATGGAGAAATCTCGCCTTTACTAAAAATACAAAATTAGCCAGGCGTGGTGGC CAGCCTGACCAATATGGAGAAATCTCGCCTTTGCTAAAAATACAAAATTAGCCAGGCGTGGTGGC A G SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1292987006 Functional Loss SNV dbSNP153 33..33 33 - - - 89217 RMVar_ID_89217 Human_SNP_ID_281743779 m1A Human chr6 + 70667945 70667945 70667945 GGGCTGAGTCCGCCCGCGGTCCCGGCGGCGCCAGGTGCGTTCACTCTGCCCGGCTCCAGCCAGCG GGGCTGAGTCCGCCCGCGGTCCCGGCGGCGCCCGGTGCGTTCACTCTGCCCGGCTCCAGCCAGCG A C SMAP1 Ensembl:ENSG00000112305 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:70667809..70668073 26863196 MeRIP-seq:(Medium) rs974239114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904993,Human_RBP_ID_26828623 89218 RMVar_ID_89218 Human_SNP_ID_281743780 m1A Human chr6 + 70667945 70667945 70667945 GGGCTGAGTCCGCCCGCGGTCCCGGCGGCGCCAGGTGCGTTCACTCTGCCCGGCTCCAGCCAGCG GGGCTGAGTCCGCCCGCGGTCCCGGCGGCGCCGGGTGCGTTCACTCTGCCCGGCTCCAGCCAGCG A G SMAP1 Ensembl:ENSG00000112305 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:70667809..70668073 26863196 MeRIP-seq:(Medium) rs974239114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904993,Human_RBP_ID_26828623 89219 RMVar_ID_89219 Human_SNP_ID_281743812 m1A Human chr6 + 70667992 70667992 70667992 GCCCGGCTCCAGCCAGCGTCCGCCGCCGCCGTAGCTGCCCCAGGCTCCCCGCCCCGCTGCCGAGA GCCCGGCTCCAGCCAGCGTCCGCCGCCGCCGTGGCTGCCCCAGGCTCCCCGCCCCGCTGCCGAGA A G SMAP1 Ensembl:ENSG00000112305 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:70667913..70668010 26863410 MeRIP-seq:(Medium) rs972481274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4896068,Human_RBP_ID_26828623 89220 RMVar_ID_89220 Human_SNP_ID_281743819 m1A Human chr6 + 70668001 70668001 70668001 CAGCCAGCGTCCGCCGCCGCCGTAGCTGCCCCAGGCTCCCCGCCCCGCTGCCGAGATGGCGACGC CAGCCAGCGTCCGCCGCCGCCGTAGCTGCCCCGGGCTCCCCGCCCCGCTGCCGAGATGGCGACGC A G SMAP1 Ensembl:ENSG00000112305 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr6:70667950..70668092;chr6:70667827..70668078 26863196 MeRIP-seq:(Medium) rs1243280977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904993,Human_RBP_ID_26828623 89221 RMVar_ID_89221 Human_SNP_ID_281792368 m1A Human chr6 + 70858152 70858152 70858152 TTCCTCAGAACGTTGTTGGCCCCCAAGGAGGAATGGTGGGACAAATGGGTGCACCCCAGAGTAAG TTCCTCAGAACGTTGTTGGCCCCCAAGGAGGAGTGGTGGGACAAATGGGTGCACCCCAGAGTAAG A G SMAP1 Ensembl:ENSG00000112305 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:70858051..70859350 32194978 MeRIP-seq:(Medium) rs1448817510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_784841,Human_Splice_Rec_784861,Human_Splice_Rec_784881,Human_Splice_Rec_784901 89222 RMVar_ID_89222 Human_SNP_ID_281902784 m1A Human chr6 + 71289079 71289079 71289079 CGGCGGCAGCGAGGGCCCGGGGCAGGAGTCCGAGCAGCCCGCGCAGCCCCCGGAGCAAGCCGGCG CGGCGGCAGCGAGGGCCCGGGGCAGGAGTCCGGGCAGCCCGCGCAGCCCCCGGAGCAAGCCGGCG A G OGFRL1 Ensembl:ENSG00000119900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:71288853..71289207;chr6:71288826..71289213 26863196 MeRIP-seq:(Medium) rs1245507279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252127 Human_Splice_Rec_785127 89223 RMVar_ID_89223 Human_SNP_ID_281902785 m1A Human chr6 + 71289079 71289079 71289079 CGGCGGCAGCGAGGGCCCGGGGCAGGAGTCCGAGCAGCCCGCGCAGCCCCCGGAGCAAGCCGGCG CGGCGGCAGCGAGGGCCCGGGGCAGGAGTCCGTGCAGCCCGCGCAGCCCCCGGAGCAAGCCGGCG A T OGFRL1 Ensembl:ENSG00000119900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:71288853..71289207;chr6:71288826..71289213 26863196 MeRIP-seq:(Medium) rs1245507279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252127 Human_Splice_Rec_785127 89224 RMVar_ID_89224 Human_SNP_ID_281903753 m1A Human chr6 - 71293340 71293340 71293340 TGGTGTCGGTACTTGTACAAATCCCTGGCAGCATAAAAACTTCTCTTTGGTTTGGCAGTTGCTTC TGGTGTCGGTACTTGTACAAATCCCTGGCAGCTTAAAAACTTCTCTTTGGTTTGGCAGTTGCTTC T A AL589935.1 Ensembl:ENSG00000232295 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:71293276..71293375 26863196 MeRIP-seq:(Medium) rs776864339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17297,RMVar_hsa_circ_66466 89225 RMVar_ID_89225 Human_SNP_ID_281934597 m1A Human chr6 - 71420699 71420699 71420699 CCGGTTGCCTACCGGCCGCTTCTCGCCGAGGCAGTCCAGACTTTTCCCCCGGCGGTGCCCGCTCC CCGGTTGCCTACCGGCCGCTTCTCGCCGAGGCTGTCCAGACTTTTCCCCCGGCGGTGCCCGCTCC T A LINC00472 Ensembl:ENSG00000233237 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:71420651..71420782 26863196 MeRIP-seq:(Medium) rs1455867316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3823255,Human_RBP_ID_5621756 89226 RMVar_ID_89226 Human_SNP_ID_282374220 m1A Human chr6 - 73242506 73242506 73242506 TGTATCAGGTCGGAGCAGAGCATGGACATGGGAACGAGTGCTCTCAGCAAGAAGCCGTGGTGGAC TGTATCAGGTCGGAGCAGAGCATGGACATGGGGACGAGTGCTCTCAGCAAGAAGCCGTGGTGGAC T C AL365232.1,KHDC1 Ensembl:ENSG00000243501,Ensembl:ENSG00000135314 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:73242457..73262800 26863196 MeRIP-seq:(Medium) rs759682596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_786338,Human_Splice_Rec_786358,Human_Splice_Rec_786366,Human_Splice_Rec_786376,Human_Splice_Rec_786382 89227 RMVar_ID_89227 Human_SNP_ID_282379049 m1A Human chr6 + 73263070 73263043 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCG___________________________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCGGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1041596223 Functional Loss DEL dbSNP153 7..33 33 - - - 89228 RMVar_ID_89228 Human_SNP_ID_282379050 m1A Human chr6 + 73263070 73263046 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCG________________________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1241500823 Functional Loss DEL dbSNP153 10..33 33 - - - 89229 RMVar_ID_89229 Human_SNP_ID_282379055 m1A Human chr6 + 73263070 73263052 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCG__________________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1343928870 Functional Loss DEL dbSNP153 16..33 33 - - - 89230 RMVar_ID_89230 Human_SNP_ID_282379060 m1A Human chr6 + 73263070 73263055 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCG_______________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs574127460 Functional Loss DEL dbSNP153 19..33 33 - - - 89231 RMVar_ID_89231 Human_SNP_ID_282379063 m1A Human chr6 + 73263070 73263058 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCG____________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1355667500 Functional Loss DEL dbSNP153 22..33 33 - - - 89232 RMVar_ID_89232 Human_SNP_ID_282379065 m1A Human chr6 + 73263070 73263061 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCGGCG_________GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1187731275 Functional Loss DEL dbSNP153 25..33 33 - - - 89233 RMVar_ID_89233 Human_SNP_ID_282379070 m1A Human chr6 + 73263070 73263064 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCGGCGGCG______GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCGGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs891033989 Functional Loss DEL dbSNP153 28..33 33 - - - 89234 RMVar_ID_89234 Human_SNP_ID_282379077 m1A Human chr6 + 73263070 73263067 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCGGCGGCGGCG___GCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG GGCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs1554225337 Functional Loss DEL dbSNP153 31..33 33 - - - 89235 RMVar_ID_89235 Human_SNP_ID_282379079 m1A Human chr6 + 73263070 73263070 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs28641970 Functional Loss SNV dbSNP153 33..33 33 - - - 89236 RMVar_ID_89236 Human_SNP_ID_282379080 m1A Human chr6 + 73263070 73263070 73263070 AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG AGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGCGGCGGCAGCGGCTGCAGGCCTGGCCGATTG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:73262970..73263099 26863196 MeRIP-seq:(Medium) rs28641970 Functional Loss SNV dbSNP153 33..33 33 - - - 89237 RMVar_ID_89237 Human_SNP_ID_282379196 m1A Human chr6 - 73263363 73263363 73263363 CAATGGGGGTCGTCCGGGTCTGGGTCATTGCCACTGGCTCGTCCCTCCTCCCACCCTTGCTTCCT CAATGGGGGTCGTCCGGGTCTGGGTCATTGCCCCTGGCTCGTCCCTCCTCCCACCCTTGCTTCCT T G KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:73263264..73263445;chr6:73263239..73263380 26863196 MeRIP-seq:(Medium) rs912365514 Functional Loss SNV dbSNP153 33..33 33 - - - 89238 RMVar_ID_89238 Human_SNP_ID_282388659 m1A Human chr6 - 73300309 73300309 73300309 TGGTGTGGAAAGTGGAAGGGGGAATGAGCTACAAAGCTACGAAGGAAAAGTGAACCGTAAGTGCA TGGTGTGGAAAGTGGAAGGGGGAATGAGCTACCAAGCTACGAAGGAAAAGTGAACCGTAAGTGCA T G KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:73300259..73300346 26863196 MeRIP-seq:(Medium) rs1411130866 Functional Loss SNV dbSNP153 33..33 33 - - - 89239 RMVar_ID_89239 Human_SNP_ID_282446136 m1A Human chr6 + 73518753 73518753 73518753 AGAGGCAGGCGCAAGGGCTTGTCAGTTGGACGAGTTGGTGGTAGGATGCAGTCCAGAGCCTCAAG AGAGGCAGGCGCAAGGGCTTGTCAGTTGGACGGGTTGGTGGTAGGATGCAGTCCAGAGCCTCAAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:73518726..73518800 32194978 MeRIP-seq:(Medium) rs1341004494 Functional Loss SNV dbSNP153 33..33 33 - - - 89240 RMVar_ID_89240 Human_SNP_ID_282446412 m1A Human chr6 + 73519369 73519369 73519369 CTGAGATGTCCCTGTAATCATGTTTTTGATAAAGTCTCTGTGTCCTGGGGCATCAATGATAGTCA CTGAGATGTCCCTGTAATCATGTTTTTGATAAGGTCTCTGTGTCCTGGGGCATCAATGATAGTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:73519241..73519371 26863196 MeRIP-seq:(Medium) rs11550789 Functional Loss SNV dbSNP153 33..33 33 - - - 89241 RMVar_ID_89241 Human_SNP_ID_282446977 m1A Human chr6 - 73520616 73520616 73520616 TGGTATTTCGGTTTTTGGGGCCGCGGGCGGCGACGGGGCCCGTGCGTCCCAGCGCACATGTTCGG TGGTATTTCGGTTTTTGGGGCCGCGGGCGGCGGCGGGGCCCGTGCGTCCCAGCGCACATGTTCGG T C EEF1A1 Ensembl:ENSG00000156508 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:73520578..73520669;chr6:73520565..73520655 26863196 MeRIP-seq:(Medium) rs1158397892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251675,Human_RBP_ID_790536,Human_RBP_ID_841444,Human_RBP_ID_951276,Human_RBP_ID_4897001,Human_RBP_ID_7627240,Human_RBP_ID_15941932,Human_RBP_ID_18425922,Human_RBP_ID_18502680,Human_RBP_ID_19133894,Human_RBP_ID_22314445,Human_RBP_ID_27842470 RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_82325,RMVar_hsa_circ_239520,RMVar_hsa_circ_79509,RMVar_hsa_circ_239521,RMVar_hsa_circ_79498,RMVar_hsa_circ_110289,RMVar_hsa_circ_239530,RMVar_hsa_circ_239531,RMVar_hsa_circ_99543,RMVar_hsa_circ_120353,RMVar_hsa_circ_239533,RMVar_hsa_circ_239537,RMVar_hsa_circ_109744,RMVar_hsa_circ_239538 89242 RMVar_ID_89242 Human_SNP_ID_282447144 m1A Human chr6 + 73520963 73520962 73520964 AATTCAAGGCACGCAAGGGCCATAACCCGTAAAGAGGCCAGGCCCGCGGGAACCACACACGGCAC AATTCAAGGCACGCAAGGGCCATAACCCGTAA__AGGCCAGGCCCGCGGGAACCACACACGGCAC AAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:73520950..73521177 26863196 MeRIP-seq:(Medium) rs868542644 Functional Loss DEL dbSNP153 33..34 33 - - - 89243 RMVar_ID_89243 Human_SNP_ID_282447145 m1A Human chr6 + 73520963 73520963 73520963 AATTCAAGGCACGCAAGGGCCATAACCCGTAAAGAGGCCAGGCCCGCGGGAACCACACACGGCAC AATTCAAGGCACGCAAGGGCCATAACCCGTAATGAGGCCAGGCCCGCGGGAACCACACACGGCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:73520950..73521177 26863196 MeRIP-seq:(Medium) rs1561964166 Functional Loss SNV dbSNP153 33..33 33 - - - 89244 RMVar_ID_89244 Human_SNP_ID_282491809 m1A Human chr6 - 73696235 73696235 73696235 CGGTGCACACGCAGAGGAGGTGGGCGGCGGTCAGGAGCGGTGGGCCCTGCATCTCGACGGCGTCT CGGTGCACACGCAGAGGAGGTGGGCGGCGGTCGGGAGCGGTGGGCCCTGCATCTCGACGGCGTCT T C RF00017-4489,lnc-BBS5-6,LOC101928489 RNACentral:URS00009982F9,RNACentral:URS0000E2127A,RNACentral:URS0000D576E5 SRP RNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:73696125..73696288 26863196 MeRIP-seq:(Medium) rs778804944 Functional Loss SNV dbSNP153 33..33 33 - - - 89245 RMVar_ID_89245 Human_SNP_ID_282491810 m1A Human chr6 - 73696235 73696235 73696235 CGGTGCACACGCAGAGGAGGTGGGCGGCGGTCAGGAGCGGTGGGCCCTGCATCTCGACGGCGTCT CGGTGCACACGCAGAGGAGGTGGGCGGCGGTCCGGAGCGGTGGGCCCTGCATCTCGACGGCGTCT T G RF00017-4489,lnc-BBS5-6,LOC101928489 RNACentral:URS00009982F9,RNACentral:URS0000E2127A,RNACentral:URS0000D576E5 SRP RNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:73696125..73696288 26863196 MeRIP-seq:(Medium) rs778804944 Functional Loss SNV dbSNP153 33..33 33 - - - 89246 RMVar_ID_89246 Human_SNP_ID_282492164 m1A Human chr6 - 73697382 73697382 73697382 ACCAGAAACCGAGGCCTAAAGAGTTCCCAACAAGGGAAAAACAAAGTTTCTTATCCTCACATCTC ACCAGAAACCGAGGCCTAAAGAGTTCCCAACATGGGAAAAACAAAGTTTCTTATCCTCACATCTC T A RF00017-4489,lnc-BBS5-6 RNACentral:URS00009982F9,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:73697367..73697452 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89247 RMVar_ID_89247 Human_SNP_ID_282492165 m1A Human chr6 - 73697382 73697382 73697382 ACCAGAAACCGAGGCCTAAAGAGTTCCCAACAAGGGAAAAACAAAGTTTCTTATCCTCACATCTC ACCAGAAACCGAGGCCTAAAGAGTTCCCAACACGGGAAAAACAAAGTTTCTTATCCTCACATCTC T G RF00017-4489,lnc-BBS5-6 RNACentral:URS00009982F9,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:73697367..73697452 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89248 RMVar_ID_89248 Human_SNP_ID_503888420 m1A Human chr12 - 62260143 62260143 62260143 GGACTGCCGGGTTTTAGCTTTCCTCGCCGCCGAGGGCTCTGGCTCTCTCTCGCTAGAGGGATGCC GGACTGCCGGGTTTTAGCTTTCCTCGCCGCCGCGGGCTCTGGCTCTCTCTCGCTAGAGGGATGCC T G TAFA2 Ensembl:ENSG00000198673 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:62260095..62260188 26863196 MeRIP-seq:(Medium) rs1436975787 Functional Loss SNV dbSNP153 33..33 33 - - - 89249 RMVar_ID_89249 Human_SNP_ID_503938579 m1A Human chr12 - 62466998 62466998 62466998 CACCTCTGGCTTTTCTCGGAGGCGCCCCCCGCAGTCGCACCGTCCCGCTAGGCTCCGCCGACTCT CACCTCTGGCTTTTCTCGGAGGCGCCCCCCGCCGTCGCACCGTCCCGCTAGGCTCCGCCGACTCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:62466860..62467001;chr12:62466871..62467094 26863196 MeRIP-seq:(Medium) rs1382781245 Functional Loss SNV dbSNP153 33..33 33 - - - 89250 RMVar_ID_89250 Human_SNP_ID_503970008 m1A Human chr12 - 62603132 62603132 62603132 TACCCGGGCCCCCACCCGCGCCGCGCTGTCGAACCCGCCGCCGGCCCGCTCTCGGCGCCGATAAT TACCCGGGCCCCCACCCGCGCCGCGCTGTCGACCCCGCCGCCGGCCCGCTCTCGGCGCCGATAAT T G LINC01465 Ensembl:ENSG00000221949 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:62603043..62603176 26863196 MeRIP-seq:(Medium) rs898153425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5173135 89251 RMVar_ID_89251 Human_SNP_ID_503973013 m1A Human chr12 - 62614143 62614143 62614143 TTATCTGTCCCTTTGTCCCCAGATTCCTATACAGCATCTACATTAGACTACTTGCTCTTCCTTGA TTATCTGTCCCTTTGTCCCCAGATTCCTATACGGCATCTACATTAGACTACTTGCTCTTCCTTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:62614092..62614188 26863196 MeRIP-seq:(Medium) rs1346268204 Functional Loss SNV dbSNP153 33..33 33 - - - 89252 RMVar_ID_89252 Human_SNP_ID_504048857 m1A Human chr12 - 62934615 62934615 62934615 CGGAGGCTCGGACCTGCCCCTGCGTTTCCCCTACGGGCGGCCAGAGTTCCTGGGGCTGTCTCAGG CGGAGGCTCGGACCTGCCCCTGCGTTTCCCCTGCGGGCGGCCAGAGTTCCTGGGGCTGTCTCAGG T C PPM1H Ensembl:ENSG00000111110 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:62934567..62935070 26863196 MeRIP-seq:(Medium) rs771839014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4236111 89253 RMVar_ID_89253 Human_SNP_ID_504048950 m1A Human chr12 + 62934798 62934798 62934798 GAGCAGGAGGCGGCGGGGGCCGGGCAAGGCGCAGCGCGGGGCATGCAGGCTGCGGTGGGCGCCGG GAGCAGGAGGCGGCGGGGGCCGGGCAAGGCGCTGCGCGGGGCATGCAGGCTGCGGTGGGCGCCGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:62934750..62934851;chr12:62934756..62934857 26863196 MeRIP-seq:(Medium) rs1444771171 Functional Loss SNV dbSNP153 33..33 33 - - - 89254 RMVar_ID_89254 Human_SNP_ID_504048996 m1A Human chr12 + 62934953 62934953 62934953 GTGCCGCGGTGGCCGCCGCCTCCCCCCGCTACACTTCCGCAACGGAGCTGCATGGAGCGGGCCGA GTGCCGCGGTGGCCGCCGCCTCCCCCCGCTACCCTTCCGCAACGGAGCTGCATGGAGCGGGCCGA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:62934916..62935047 26863196 MeRIP-seq:(Medium) rs946793580 Functional Loss SNV dbSNP153 33..33 33 - - - 89255 RMVar_ID_89255 Human_SNP_ID_504049016 m1A Human chr12 - 62935026 62935026 62935026 CAGGGGGCGGGGAAGGGACCTGCTGCAGCTGCAGCCGCCTGGGCGCTCCTGGAGCGCGCGGTGAC CAGGGGGCGGGGAAGGGACCTGCTGCAGCTGCGGCCGCCTGGGCGCTCCTGGAGCGCGCGGTGAC T C PPM1H Ensembl:ENSG00000111110 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:62934979..62935124 26863196 MeRIP-seq:(Medium) rs1301692904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247612 89256 RMVar_ID_89256 Human_SNP_ID_504056378 m1A Human chr12 + 62965319 62965319 62965319 AAAAGATAATAGTGGCCTTCTCACCTAACGCCACCAACATGGTGTTCAGGCGCTTCGTGGAGGTT AAAAGATAATAGTGGCCTTCTCACCTAACGCCGCCAACATGGTGTTCAGGCGCTTCGTGGAGGTT A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878991008 Functional Loss SNV dbSNP153 33..33 33 - - - 89257 RMVar_ID_89257 Human_SNP_ID_504301133 m1A Human chr12 + 63999939 63999939 63999939 GGATAAGAAGAAGAACTGTATCCTATAAAATGACTGAGAAGGATCAGCCAGAGAGGTGAGAAGAA GGATAAGAAGAAGAACTGTATCCTATAAAATGCCTGAGAAGGATCAGCCAGAGAGGTGAGAAGAA A C SRGAP1 Ensembl:ENSG00000196935 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:63999892..63999960 26863196 MeRIP-seq:(Medium) rs1429247937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5953,RMVar_hsa_circ_301016,RMVar_hsa_circ_318531,RMVar_hsa_circ_341481,RMVar_hsa_circ_45548,RMVar_hsa_circ_291827,RMVar_hsa_circ_157857,RMVar_hsa_circ_157858 89258 RMVar_ID_89258 Human_SNP_ID_504303699 m1A Human chr12 - 64010994 64010994 64010994 GCTGGTACAATCCTACATGTAACTCTGTAAAAACTTTCTGGTAACTTCAACTTGCCCCCAAGGAA GCTGGTACAATCCTACATGTAACTCTGTAAAAGCTTTCTGGTAACTTCAACTTGCCCCCAAGGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:64010988..64011121 26863196 MeRIP-seq:(Medium) rs1005502339 Functional Loss SNV dbSNP153 33..33 33 - - - 89259 RMVar_ID_89259 Human_SNP_ID_504394784 m1A Human chr12 + 64404701 64404701 64404701 AGCTGCGGCCGTGGCGGAGGACTACGGCGACAAGGACGAGGGCCGCTCTCCCAGCTCTCTGCGTG AGCTGCGGCCGTGGCGGAGGACTACGGCGACAGGGACGAGGGCCGCTCTCCCAGCTCTCTGCGTG A G XPOT Ensembl:ENSG00000184575 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:64404651..64404725 32194978 MeRIP-seq:(Medium) rs1309327165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229390,Human_RBP_ID_1475502,Human_RBP_ID_4246197,Human_RBP_ID_6206982,Human_RBP_ID_8784141,Human_RBP_ID_9255532,Human_RBP_ID_9279122,Human_RBP_ID_9322610,Human_RBP_ID_12003321,Human_RBP_ID_17824416,Human_RBP_ID_18631141 RMVar_hsa_circ_82472,RMVar_hsa_circ_106107,RMVar_hsa_circ_157897,RMVar_hsa_circ_157898 89260 RMVar_ID_89260 Human_SNP_ID_504394794 m1A Human chr12 + 64404721 64404721 64404721 ACTACGGCGACAAGGACGAGGGCCGCTCTCCCAGCTCTCTGCGTGCCGCGCCGCTCCGCTCCGCT ACTACGGCGACAAGGACGAGGGCCGCTCTCCCGGCTCTCTGCGTGCCGCGCCGCTCCGCTCCGCT A G XPOT Ensembl:ENSG00000184575 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:64404426..64404761 26863196 MeRIP-seq:(Medium) rs994790759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3349,Human_RBP_ID_229390,Human_RBP_ID_425438,Human_RBP_ID_811386,Human_RBP_ID_1475502,Human_RBP_ID_4236445,Human_RBP_ID_6206982,Human_RBP_ID_8784141,Human_RBP_ID_9255532,Human_RBP_ID_9279122,Human_RBP_ID_9322610,Human_RBP_ID_12003322,Human_RBP_ID_17824416,Human_RBP_ID_18631142 Human_Splice_Rec_1392791 RMVar_hsa_circ_82472,RMVar_hsa_circ_106107,RMVar_hsa_circ_157897,RMVar_hsa_circ_157898 89261 RMVar_ID_89261 Human_SNP_ID_504394825 m1A Human chr12 + 64404798 64404798 64404798 GGAGTGCAGGCTGGGAGGCGGGATGGAGTGATAGGGAAGGTGACTCGGGGCTCGGGGGCAGCGGG GGAGTGCAGGCTGGGAGGCGGGATGGAGTGATGGGGAAGGTGACTCGGGGCTCGGGGGCAGCGGG A G XPOT Ensembl:ENSG00000184575 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:64404747..64405088 32194978 MeRIP-seq:(Medium) rs914167587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229391,Human_RBP_ID_878563,Human_RBP_ID_6206984,Human_RBP_ID_9416122,Human_RBP_ID_22574825,Human_RBP_ID_22795025,Human_RBP_ID_23269818,Human_RBP_ID_24364771,Human_RBP_ID_26776851 Human_Splice_Rec_1392791 RMVar_hsa_circ_82472,RMVar_hsa_circ_106107,RMVar_hsa_circ_157897,RMVar_hsa_circ_157898 89262 RMVar_ID_89262 Human_SNP_ID_504394838 m1A Human chr12 + 64404825 64404825 64404825 GTGATAGGGAAGGTGACTCGGGGCTCGGGGGCAGCGGGACCGGGACCAGGTTTGGTCCGCGTGAG GTGATAGGGAAGGTGACTCGGGGCTCGGGGGCCGCGGGACCGGGACCAGGTTTGGTCCGCGTGAG A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:64404819..64404967 26863196 MeRIP-seq:(Medium) rs931163676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229392,Human_RBP_ID_754396,Human_RBP_ID_811387,Human_RBP_ID_878563,Human_RBP_ID_5349894,Human_RBP_ID_9416122,Human_RBP_ID_22040013,Human_RBP_ID_23269818,Human_RBP_ID_24364771,Human_RBP_ID_26776851 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 89263 RMVar_ID_89263 Human_SNP_ID_504400117 m1A Human chr12 + 64425369 64425369 64425369 GCTGGTAACATCAGGAGTCAGTTCCTATCAGCATACATCTGTGACATTGGAGTTCTTCGAAACTG GCTGGTAACATCAGGAGTCAGTTCCTATCAGCGTACATCTGTGACATTGGAGTTCTTCGAAACTG A G XPOT Ensembl:ENSG00000184575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:64425338..64425439 32194978 MeRIP-seq:(Medium) rs775942611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_993847,Human_RBP_ID_1475592,Human_RBP_ID_6207218,Human_RBP_ID_8381460,Human_RBP_ID_8784157,Human_RBP_ID_17240018,Human_RBP_ID_18631171,Human_RBP_ID_22574830,Human_RBP_ID_22912597,Human_RBP_ID_24557647,Human_RBP_ID_25016236,Human_RBP_ID_27631679 Human_Splice_Rec_1392814,Human_Splice_Rec_1392815,Human_Splice_Rec_1392855,Human_Splice_Rec_1392868,Human_Splice_Rec_1392869 Human_miRNA_ID_2379472,Human_miRNA_ID_3012418 RMVar_hsa_circ_17784,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_366999,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,RMVar_hsa_circ_310416,RMVar_hsa_circ_74887,RMVar_hsa_circ_295877,RMVar_hsa_circ_63505,RMVar_hsa_circ_39289,RMVar_hsa_circ_33371,RMVar_hsa_circ_157899,RMVar_hsa_circ_116546,RMVar_hsa_circ_157908,RMVar_hsa_circ_80366,RMVar_hsa_circ_100708,RMVar_hsa_circ_157910,RMVar_hsa_circ_157909,RMVar_hsa_circ_292698,RMVar_hsa_circ_332727,RMVar_hsa_circ_157912,RMVar_hsa_circ_116565,RMVar_hsa_circ_340024,RMVar_hsa_circ_375018,RMVar_hsa_circ_328343,RMVar_hsa_circ_19183,RMVar_hsa_circ_56520,RMVar_hsa_circ_157913,RMVar_hsa_circ_157914,RMVar_hsa_circ_87887,RMVar_hsa_circ_48298,RMVar_hsa_circ_102742,RMVar_hsa_circ_157915,RMVar_hsa_circ_92357,RMVar_hsa_circ_157916,RMVar_hsa_circ_157919,RMVar_hsa_circ_111736,RMVar_hsa_circ_127547,RMVar_hsa_circ_157917,RMVar_hsa_circ_125827,RMVar_hsa_circ_157921,RMVar_hsa_circ_81030,RMVar_hsa_circ_157920,RMVar_hsa_circ_157918 89264 RMVar_ID_89264 Human_SNP_ID_504444894 m1A Human chr12 + 64610624 64610624 64610624 GCGCCCCGGGGAGGCCGCCCGCGCGCGACGGGACCGGCAGCATGAGCAGCGGCTACAGCAGCCTG GCGCCCCGGGGAGGCCGCCCGCGCGCGACGGGTCCGGCAGCATGAGCAGCGGCTACAGCAGCCTG A T RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:64610424..64610680;chr12:64610331..64610738 26863196 MeRIP-seq:(Medium) rs757225093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246200,Human_RBP_ID_8940719,Human_RBP_ID_18417295,Human_RBP_ID_22040015 89265 RMVar_ID_89265 Human_SNP_ID_504450158 m1A Human chr12 + 64632043 64632040 64632043 AGAAAGAAGACGTCTCTCCCATCGTTGAGTGGAGGAGAAGTTCAATCTAGAAATGTGTATATAAT AGAAAGAAGACGTCTCTCCCATCGTTGAGT___GGAGAAGTTCAATCTAGAAATGTGTATATAAT TGGA T RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:64632040..64632302 26863196 MeRIP-seq:(Medium) rs1189225601 Functional Loss DEL dbSNP153 31..33 33 - - - 89266 RMVar_ID_89266 Human_SNP_ID_504450246 m1A Human chr12 + 64632403 64632403 64632403 GGGAGAAATAAAGTGGTCAGACCTATGATTTTAAAACTGACAGCAGAGTTTAGAGGGCAAGAGGG GGGAGAAATAAAGTGGTCAGACCTATGATTTTTAAACTGACAGCAGAGTTTAGAGGGCAAGAGGG A T RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:64632400..64632695 26863196 MeRIP-seq:(Medium) rs182723925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6207776 89267 RMVar_ID_89267 Human_SNP_ID_504466252 m1A Human chr12 - 64695562 64695560 64695563 ACTGAATGCTTTTAACTCGTTTACAAGCAACTACCCCTTTCTCCACTACCCCTAACTGAAAAGCC ACTGAATGCTTTTAACTCGTTTACAAGCAAC___CCCTTTCTCCACTACCCCTAACTGAAAAGCC GGTA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:64695472..64695682 26863196 MeRIP-seq:(Medium) rs1223677268 Functional Loss DEL dbSNP153 32..34 33 - - - 89268 RMVar_ID_89268 Human_SNP_ID_504479224 m1A Human chr12 + 64747916 64747916 64747916 GCTCTGCTGGGGCAGCAGAGAGCACTTGGCACATACTACAAAGGAAAGGAAGCAAAAACGACAAA GCTCTGCTGGGGCAGCAGAGAGCACTTGGCACCTACTACAAAGGAAAGGAAGCAAAAACGACAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:64747851..64747925 32194978 MeRIP-seq:(Medium) rs765701552 Functional Loss SNV dbSNP153 33..33 33 - - - 89269 RMVar_ID_89269 Human_SNP_ID_504479225 m1A Human chr12 + 64747916 64747916 64747916 GCTCTGCTGGGGCAGCAGAGAGCACTTGGCACATACTACAAAGGAAAGGAAGCAAAAACGACAAA GCTCTGCTGGGGCAGCAGAGAGCACTTGGCACGTACTACAAAGGAAAGGAAGCAAAAACGACAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:64747851..64747925 32194978 MeRIP-seq:(Medium) rs765701552 Functional Loss SNV dbSNP153 33..33 33 - - - 89270 RMVar_ID_89270 Human_SNP_ID_504482252 m1A Human chr12 + 64759310 64759300 64759310 GCGGACAGGCTCCGGGGTGACCCCGGGACGGGACGGGACGGAGGGACGCACAGGTAGCTGAAGGG GCGGACAGGCTCCGGGGTGACCC__________CGGGACGGAGGGACGCACAGGTAGCTGAAGGG CCGGGACGGGA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:64759178..64759375 26863196 MeRIP-seq:(Medium) rs559286032 Functional Loss DEL dbSNP153 24..33 33 - - - Clinvar_Rec_504 89271 RMVar_ID_89271 Human_SNP_ID_504482265 m1A Human chr12 + 64759329 64759329 64759329 ACCCCGGGACGGGACGGGACGGAGGGACGCACAGGTAGCTGAAGGGCGAGAGGCCGACCAGCCGA ACCCCGGGACGGGACGGGACGGAGGGACGCACGGGTAGCTGAAGGGCGAGAGGCCGACCAGCCGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:64759278..64759381 26863196 MeRIP-seq:(Medium) rs1461938162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22907038 89272 RMVar_ID_89272 Human_SNP_ID_504487378 m1A Human chr12 - 64780816 64780816 64780816 GGAGCCCCGGGCGGCCCCCGCCGGTGGGAAGGACGTCCATGGTCCCCGGCGCGCGGCTGCCCGGC GGAGCCCCGGGCGGCCCCCGCCGGTGGGAAGGTCGTCCATGGTCCCCGGCGCGCGGCTGCCCGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:64780593..64781267;chr12:64780593..64781248 26863196 MeRIP-seq:(Medium) rs1330037708 Functional Loss SNV dbSNP153 33..33 33 - - - 89273 RMVar_ID_89273 Human_SNP_ID_504488618 m1A Human chr12 + 64785821 64785821 64785821 GGATGTTCTATTTATCTTTGGACTAATATCACACTGGAATTTGTATTCCTCTCAAGGTATTAATC GGATGTTCTATTTATCTTTGGACTAATATCACGCTGGAATTTGTATTCCTCTCAAGGTATTAATC A G TBC1D30,AC078815.1 Ensembl:ENSG00000111490,Ensembl:ENSG00000288591 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:64785809..64785896 26863196 MeRIP-seq:(Medium) rs1278394263 Functional Loss SNV dbSNP153 33..33 33 - - - 89274 RMVar_ID_89274 Human_SNP_ID_504577489 m1A Human chr12 - 65169868 65169868 65169868 GTAAGTAGGAGAGGTCGCCCGAGACCGGCCGGACCCCCATCCCCGCGGCCGCCGCCGCCGCTGGT GTAAGTAGGAGAGGTCGCCCGAGACCGGCCGGCCCCCCATCCCCGCGGCCGCCGCCGCCGCTGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:65169818..65169919 26863196 MeRIP-seq:(Medium) rs1021033238 Functional Loss SNV dbSNP153 33..33 33 - - - 89275 RMVar_ID_89275 Human_SNP_ID_504577692 m1A Human chr12 + 65170300 65170300 65170300 AGAGGACGGTGAGGAGAGGGACCCGGAGACCGAGGAGCCGCTCTGGGCGAGCCGGACCGTGAATG AGAGGACGGTGAGGAGAGGGACCCGGAGACCGGGGAGCCGCTCTGGGCGAGCCGGACCGTGAATG A G LEMD3 Ensembl:ENSG00000174106 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:65170067..65170373 26863196 MeRIP-seq:(Medium) rs751372115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_195322,Human_RBP_ID_230101,Human_RBP_ID_3943279,Human_RBP_ID_5139668,Human_RBP_ID_5521638,Human_RBP_ID_8381661,Human_RBP_ID_9279126,Human_RBP_ID_18975944,Human_RBP_ID_22040621,Human_RBP_ID_22436622,Human_RBP_ID_26321692,Human_RBP_ID_26768263 89276 RMVar_ID_89276 Human_SNP_ID_504577777 m1A Human chr12 - 65170466 65170466 65170466 GATTTAGCAGTCAGCGGGGGGAGAGGCTTACTATGGGTTCGTCTGGGCCGATGCCGGGAAAGGGA GATTTAGCAGTCAGCGGGGGGAGAGGCTTACTGTGGGTTCGTCTGGGCCGATGCCGGGAAAGGGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:65170364..65170465 32194978 MeRIP-seq:(Medium) rs147328826 Functional Loss SNV dbSNP153 33..33 33 - - - 89277 RMVar_ID_89277 Human_SNP_ID_504577863 m1A Human chr12 + 65170603 65170603 65170603 CGGGAGTCTAGACAGGAGCCGAAACCTCGAAGAGGCGGCGGCCGCGGAGCAGGGAGGAGGGTGTG CGGGAGTCTAGACAGGAGCCGAAACCTCGAAGGGGCGGCGGCCGCGGAGCAGGGAGGAGGGTGTG A G LEMD3 Ensembl:ENSG00000174106 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:65170563..65170763 26863196 MeRIP-seq:(Medium) rs1185924736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22910559 89278 RMVar_ID_89278 Human_SNP_ID_504603440 m1A Human chr12 - 65278770 65278770 65278770 AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCATGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCTTGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:65278726..65278843 26863196 MeRIP-seq:(Medium) rs949229098 Functional Loss SNV dbSNP153 33..33 33 - - - 89279 RMVar_ID_89279 Human_SNP_ID_504603441 m1A Human chr12 - 65278770 65278770 65278770 AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCATGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCGTGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:65278726..65278843 26863196 MeRIP-seq:(Medium) rs949229098 Functional Loss SNV dbSNP153 33..33 33 - - - 89280 RMVar_ID_89280 Human_SNP_ID_504603442 m1A Human chr12 - 65278770 65278770 65278770 AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCATGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG AGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCCTGGAAAGGCCAGGCAGCCGCCGCCGGTGTCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:65278726..65278843 26863196 MeRIP-seq:(Medium) rs949229098 Functional Loss SNV dbSNP153 33..33 33 - - - 89281 RMVar_ID_89281 Human_SNP_ID_504603466 m1A Human chr12 - 65278800 65278799 65278800 AGAGGCAGAGGCAGAGGGAGAGGCAGAGCGAGAGGGGGCGCGGGAGGGTCCGCCGCGGGCTCATG AGAGGCAGAGGCAGAGGGAGAGGCAGAGCGAG_GGGGGCGCGGGAGGGTCCGCCGCGGGCTCATG CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:65278750..65278876 26863196 MeRIP-seq:(Medium) rs1396885453 Functional Loss DEL dbSNP153 33..33 33 - - - 89282 RMVar_ID_89282 Human_SNP_ID_504735792 m1A Human chr12 - 65825285 65825285 65825285 TGGGCTGAAGTGGACGGCTGCCCCGCGCCCTCACCGCGTGCGCTCATCCTGCCTCCCGCCGCCGC TGGGCTGAAGTGGACGGCTGCCCCGCGCCCTCGCCGCGTGCGCTCATCCTGCCTCCCGCCGCCGC T C RPSAP52 Ensembl:ENSG00000241749 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:65825252..65825351 26863196 MeRIP-seq:(Medium) rs1448432644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21968260 89283 RMVar_ID_89283 Human_SNP_ID_504790909 m1A Human chr12 + 66057686 66057686 66057686 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGACTGGAGTA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGGCGGAGTCTCACTCTGTTGCCCAGACTGGAGTA A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:66057593..66057689 26863410 MeRIP-seq:(Medium) rs568757963 Functional Loss SNV dbSNP153 33..33 33 - - - 89284 RMVar_ID_89284 Human_SNP_ID_504790910 m1A Human chr12 + 66057686 66057686 66057686 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGACTGGAGTA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGTCGGAGTCTCACTCTGTTGCCCAGACTGGAGTA A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:66057593..66057689 26863410 MeRIP-seq:(Medium) rs568757963 Functional Loss SNV dbSNP153 33..33 33 - - - 89285 RMVar_ID_89285 Human_SNP_ID_504809967 m1A Human chr12 + 66130708 66130708 66130708 TCACTGGACCGGTGAGGAACCGAACTCACCTGAGAAACGAACACCCACACCTCACGCTCACGCCG TCACTGGACCGGTGAGGAACCGAACTCACCTGGGAAACGAACACCCACACCTCACGCTCACGCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:66130701..66130750 26863196 MeRIP-seq:(Medium) rs1427633501 Functional Loss SNV dbSNP153 33..33 33 - - - 89286 RMVar_ID_89286 Human_SNP_ID_504819194 m1A Human chr12 + 66169921 66169921 66169921 GCTGCCATAGTTGAAGTCGTCCTCGATCGAGGAGCGAGGGTACCGGGGGTCGGGGTCAGCCATGA GCTGCCATAGTTGAAGTCGTCCTCGATCGAGGGGCGAGGGTACCGGGGGTCGGGGTCAGCCATGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:66169870..66169946 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89287 RMVar_ID_89287 Human_SNP_ID_505083656 m1A Human chr12 + 67269662 67269644 67269662 GGAGGAGCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG GGAGGAGCTCCAGTG__________________GCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG GGCGGCGGCGGCGGCGGCA G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:67269566..67269775;chr12:67269380..67269779 26863196 MeRIP-seq:(Medium) rs1284131427 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 89288 RMVar_ID_89288 Human_SNP_ID_505083671 m1A Human chr12 + 67269662 67269662 67269662 GGAGGAGCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG GGAGGAGCTCCAGTGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG A G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:67269566..67269775;chr12:67269380..67269779 26863196 MeRIP-seq:(Medium) rs1004927322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 89289 RMVar_ID_89289 Human_SNP_ID_505083675 m1A Human chr12 + 67269668 67269668 67269668 GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCGGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG A G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:67269380..67269750;chr12:67269384..67269775;chr12:67269549..67269722 26863196 MeRIP-seq:(Medium) rs746228572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 89290 RMVar_ID_89290 Human_SNP_ID_505083676 m1A Human chr12 + 67269668 67269668 67269668 GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCTGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG A T CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:67269380..67269750;chr12:67269384..67269775;chr12:67269549..67269722 26863196 MeRIP-seq:(Medium) rs746228572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 89291 RMVar_ID_89291 Human_SNP_ID_505083683 m1A Human chr12 + 67269675 67269675 67269675 TGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCGGGATCGA TGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCGGCAGCTCCAGCAGCGCCAGCAGGCGGGATCGA A G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:67269626..67269994 32194978 MeRIP-seq:(Medium) rs1327259271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 89292 RMVar_ID_89292 Human_SNP_ID_505170552 m1A Human chr12 + 67648928 67648928 67648928 GCCCGAGGAAGAGGAGGACGGCGGCGAGGAGGAGAGCGGGGGGCTCGCGGCGGCGGGCCCCGGCC GCCCGAGGAAGAGGAGGACGGCGGCGAGGAGGCGAGCGGGGGGCTCGCGGCGGCGGGCCCCGGCC A C DYRK2 Ensembl:ENSG00000127334 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:67648751..67649743;chr12:67648745..67649985 26863196 MeRIP-seq:(Medium) rs1391910500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228898,Human_RBP_ID_811317,Human_RBP_ID_4246208,Human_RBP_ID_5521639 RMVar_hsa_circ_102813,RMVar_hsa_circ_158065 89293 RMVar_ID_89293 Human_SNP_ID_505173240 m1A Human chr12 + 67658445 67658445 67658445 GTGTGATGATCCCCTTTTCCTTGACTTCTTAAAACAGTGTTTAGAGTGGGATCCTGCAGTGCGCA GTGTGATGATCCCCTTTTCCTTGACTTCTTAACACAGTGTTTAGAGTGGGATCCTGCAGTGCGCA A C DYRK2 Ensembl:ENSG00000127334 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:67658260..67658611 32194978 MeRIP-seq:(Medium) rs753315158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1358411,Human_RBP_ID_8784791,Human_RBP_ID_17825349,Human_RBP_ID_18263309,Human_RBP_ID_27217856,Human_RBP_ID_27424676 Human_miRNA_ID_286629,Human_miRNA_ID_524659,Human_miRNA_ID_1343491,Human_miRNA_ID_2060192,Human_miRNA_ID_2185588,Human_miRNA_ID_2648067,Human_miRNA_ID_2670664,Human_miRNA_ID_3101316 RMVar_hsa_circ_102813,RMVar_hsa_circ_158065 89294 RMVar_ID_89294 Human_SNP_ID_505173241 m1A Human chr12 + 67658445 67658445 67658445 GTGTGATGATCCCCTTTTCCTTGACTTCTTAAAACAGTGTTTAGAGTGGGATCCTGCAGTGCGCA GTGTGATGATCCCCTTTTCCTTGACTTCTTAAGACAGTGTTTAGAGTGGGATCCTGCAGTGCGCA A G DYRK2 Ensembl:ENSG00000127334 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:67658260..67658611 32194978 MeRIP-seq:(Medium) rs753315158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1358411,Human_RBP_ID_8784791,Human_RBP_ID_17825349,Human_RBP_ID_18263309,Human_RBP_ID_27217856,Human_RBP_ID_27424676 Human_miRNA_ID_286629,Human_miRNA_ID_524659,Human_miRNA_ID_1343491,Human_miRNA_ID_2060192,Human_miRNA_ID_2185588,Human_miRNA_ID_2648067,Human_miRNA_ID_2670664,Human_miRNA_ID_3101316 RMVar_hsa_circ_102813,RMVar_hsa_circ_158065 89295 RMVar_ID_89295 Human_SNP_ID_505178389 m1A Human chr12 + 67679501 67679501 67679501 ATTCTCCTGCCTCAGCCTTCTGAGTAGCTGGGACAACAGGCCGCCACCACACCCGGCTAATTTTT ATTCTCCTGCCTCAGCCTTCTGAGTAGCTGGGGCAACAGGCCGCCACCACACCCGGCTAATTTTT A G lnc-DYRK2-6,lnc-DYRK2-6:2 RNACentral:URS00008BCC63,RNACentral:URS00009B86A6 lincRNA,lincRNA intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:67679499..67679583 26863410 MeRIP-seq:(Medium) rs1412362149 Functional Loss SNV dbSNP153 33..33 33 - - - 89296 RMVar_ID_89296 Human_SNP_ID_505328377 m1A Human chr12 + 68311064 68311062 68311064 ATCCTATCACCTCTGCACTCTTCTCAAGTCCCAGTGTCCTTCCCTCACCAACTCATTATAATCCC ATCCTATCACCTCTGCACTCTTCTCAAGTCC__GTGTCCTTCCCTCACCAACTCATTATAATCCC CCA C lnc-NUP107-26 RNACentral:URS00008BDE2C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:68311045..68311126 26863196 MeRIP-seq:(Medium) rs758667544 Functional Loss DEL dbSNP153 32..33 33 - - - 89297 RMVar_ID_89297 Human_SNP_ID_505329338 m1A Human chr12 - 68315040 68315040 68315040 GAGAAAGAGGAGGAGGACGACAATGAAGAGGAAGGGGACAGGAAAACGGGCAAGCAGGCTTTTAT GAGAAAGAGGAGGAGGACGACAATGAAGAGGAGGGGGACAGGAAAACGGGCAAGCAGGCTTTTAT T C MDM1 Ensembl:ENSG00000111554 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:68314989..68315122;chr12:68314992..68315092 26863196 MeRIP-seq:(Medium) rs760557279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26321697 Human_Splice_Rec_1395213,Human_Splice_Rec_1395239,Human_Splice_Rec_1395267,Human_Splice_Rec_1395279 RMVar_hsa_circ_7926,RMVar_hsa_circ_358391,RMVar_hsa_circ_62767,RMVar_hsa_circ_64514,RMVar_hsa_circ_59173,RMVar_hsa_circ_17149 89298 RMVar_ID_89298 Human_SNP_ID_505401075 m1A Human chr12 - 68611013 68611003 68611013 ACCTCTCACGCTGTCACCGGGTCCCTGCAGCCAGCGTCGCCCCGCGCTCCCCCCGGGTCGCTACT ACCTCTCACGCTGTCACCGGGTCCCTGCAGCC__________CGCGCTCCCCCCGGGTCGCTACT GGGGCGACGCT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:68610921..68611285 26863196 MeRIP-seq:(Medium) rs1057430054 Functional Loss DEL dbSNP153 33..42 33 - - - 89299 RMVar_ID_89299 Human_SNP_ID_505404980 m1A Human chr12 - 68624622 68624622 68624622 TAGTAAAGATGGGGTTTCACCATGTTGGCCAGACTGGTCTCGAACTTCTGGCCTCAAGTGATCCG TAGTAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTTCTGGCCTCAAGTGATCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:68624616..68624750 26863196 MeRIP-seq:(Medium) rs184277801 Functional Loss SNV dbSNP153 33..33 33 - - - 89300 RMVar_ID_89300 Human_SNP_ID_505421186 m1A Human chr12 + 68687072 68687072 68687072 GGTTGTGTGTGGAAAAGGCTTTAGCCATGGACAGGTCAGTACTGATGGTGGCAGCTGAGCCCGAA GGTTGTGTGTGGAAAAGGCTTTAGCCATGGACCGGTCAGTACTGATGGTGGCAGCTGAGCCCGAA A C NUP107 Ensembl:ENSG00000111581 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:68687041..68687136;chr12:68687049..68687133 26863196 MeRIP-seq:(Medium) rs1223479863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1476377,Human_RBP_ID_3943284,Human_RBP_ID_4246843,Human_RBP_ID_12015700,Human_RBP_ID_18417296 Human_Splice_Rec_1395669,Human_Splice_Rec_1395719,Human_Splice_Rec_1395723,Human_Splice_Rec_1395777,Human_Splice_Rec_1395789,Human_Splice_Rec_1395803 89301 RMVar_ID_89301 Human_SNP_ID_505422042 m1A Human chr12 + 68690715 68690715 68690715 TGGAACAGGAGGGAAGTCGCCCCGACTTACGCAGTCTTCAGGGTTCTTTGGAAATCTCTCCATGG TGGAACAGGAGGGAAGTCGCCCCGACTTACGCCGTCTTCAGGGTTCTTTGGAAATCTCTCCATGG A C NUP107 Ensembl:ENSG00000111581 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:68690666..68692037 32194978 MeRIP-seq:(Medium) rs1309242640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228737,Human_RBP_ID_3941968,Human_RBP_ID_6213350,Human_RBP_ID_9366612,Human_RBP_ID_18975950,Human_RBP_ID_22911015,Human_RBP_ID_23208167 Human_Splice_Rec_1395674,Human_Splice_Rec_1395675,Human_Splice_Rec_1395728,Human_Splice_Rec_1395729,Human_Splice_Rec_1395782,Human_Splice_Rec_1395783,Human_Splice_Rec_1395794,Human_Splice_Rec_1395795,Human_Splice_Rec_1395808,Human_Splice_Rec_1395809,Human_Splice_Rec_1395857,Human_Splice_Rec_1395910,Human_Splice_Rec_1395911,Human_Splice_Rec_1395915,Human_Splice_Rec_1395919 Human_miRNA_ID_2452437 RMVar_hsa_circ_15411,RMVar_hsa_circ_118531,RMVar_hsa_circ_85344,RMVar_hsa_circ_42289,RMVar_hsa_circ_158079,RMVar_hsa_circ_330656,RMVar_hsa_circ_343933,RMVar_hsa_circ_362332,RMVar_hsa_circ_158080,RMVar_hsa_circ_361135,RMVar_hsa_circ_332266,RMVar_hsa_circ_280154,RMVar_hsa_circ_308408,RMVar_hsa_circ_72746,RMVar_hsa_circ_158082,RMVar_hsa_circ_158084,RMVar_hsa_circ_158085,RMVar_hsa_circ_158083,RMVar_hsa_circ_158081 89302 RMVar_ID_89302 Human_SNP_ID_505439969 m1A Human chr12 + 68764312 68764312 68764312 ACTAAGAAGTTCCCATTATTCTCTTTTTTTAGACAGTCTTGTTCTGTCGCCTGGACTAGAGTGCA ACTAAGAAGTTCCCATTATTCTCTTTTTTTAGGCAGTCTTGTTCTGTCGCCTGGACTAGAGTGCA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10878866 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11589,GWAS_ID_11590,GWAS_ID_11591,GWAS_ID_11592,GWAS_ID_11593 89303 RMVar_ID_89303 Human_SNP_ID_505450708 m1A Human chr12 + 68808743 68808743 68808743 CTCTCGCGGCGGTGGGGGTGGGGGTGGTTCGGAGGTCTCCGCGGGAGTTCAGGGTAAAGGTCACG CTCTCGCGGCGGTGGGGGTGGGGGTGGTTCGGGGGTCTCCGCGGGAGTTCAGGGTAAAGGTCACG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:68808727..68808836 26863196 MeRIP-seq:(Medium) rs1446700878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065348,Human_RBP_ID_3418414,Human_RBP_ID_5087281,Human_RBP_ID_5139903,Human_RBP_ID_8070861,Human_RBP_ID_8177413,Human_RBP_ID_8229629,Human_RBP_ID_9415899,Human_RBP_ID_18457268,Human_RBP_ID_18934636,Human_RBP_ID_21967110,Human_RBP_ID_26777417 89304 RMVar_ID_89304 Human_SNP_ID_505459825 m1A Human chr12 + 68843230 68843230 68843230 AATTTGAAGGAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAA AATTTGAAGGAATAAGTTCTAGCTGAAGTATTGTGAACTCCAAATAATGCTTTGAGGACCTCCAA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs147764324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4239413,Human_RBP_ID_6250994,Human_RBP_ID_17355887,Human_RBP_ID_17473347,Human_RBP_ID_17561205,Human_RBP_ID_26419385 Human_Splice_Rec_1396369 Human_miRNA_ID_1085350 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 89305 RMVar_ID_89305 Human_SNP_ID_505459964 m1A Human chr12 + 68843749 68843749 68843749 GTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTCCAAGCATTATTT GTCTGTCTCAATAAATGGCCAAAGGGATTAGTGGTTTACCTGTGGAGGTCCTCCAAGCATTATTT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11556781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214290,Human_RBP_ID_12018817,Human_RBP_ID_17561206,Human_RBP_ID_17685228,Human_RBP_ID_17825691,Human_RBP_ID_18263546,Human_RBP_ID_26421518,Human_RBP_ID_27632576 Human_Splice_Rec_1396370,Human_Splice_Rec_1396371 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 89306 RMVar_ID_89306 Human_SNP_ID_505558222 m1A Human chr12 - 69239708 69239708 69239708 CGCGTCGGCGGCGGGGACCTGGGCTCTCACGTACCTGGTTGAACTCTTCGCCGACATCCGCGTAA CGCGTCGGCGGCGGGGACCTGGGCTCTCACGTTCCTGGTTGAACTCTTCGCCGACATCCGCGTAA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:69239687..69239811 32194978 MeRIP-seq:(Medium) rs113435510 Functional Loss SNV dbSNP153 33..33 33 - - - 89307 RMVar_ID_89307 Human_SNP_ID_505558431 m1A Human chr12 - 69240167 69240167 69240167 CAAAATGGAGCGATGGGAGGAATCGGAGCCCGAGCGGCAGCGGCGGGGAAGGGGCGGCGGCGGCG CAAAATGGAGCGATGGGAGGAATCGGAGCCCGCGCGGCAGCGGCGGGGAAGGGGCGGCGGCGGCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:69240165..69240291 26863196 MeRIP-seq:(Medium) rs1383945323 Functional Loss SNV dbSNP153 33..33 33 - - - 89308 RMVar_ID_89308 Human_SNP_ID_505561561 m1A Human chr12 + 69251068 69251067 69251069 GATTTTTAAAACAAAAAGTTGAATTTGTATTCAAGTCTATTTTAGTAGTATTTTGACTTTTGTAT GATTTTTAAAACAAAAAGTTGAATTTGTATTC__GTCTATTTTAGTAGTATTTTGACTTTTGTAT CAA C CPSF6 Ensembl:ENSG00000111605 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:69251065..69251300 26863196 MeRIP-seq:(Medium) rs1232176983 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2350979,Human_RBP_ID_24998828 Human_Splice_Rec_1396579 89309 RMVar_ID_89309 Human_SNP_ID_505563533 m1A Human chr12 - 69258675 69258672 69258675 TCTCCTCGATTAGGAGGCCCAGCTAGAGGAGGAGGCAGAACCTGACCAGGAGGTGGAGGACCTGG TCTCCTCGATTAGGAGGCCCAGCTAGAGGAGG___CAGAACCTGACCAGGAGGTGGAGGACCTGG GCCT G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:69258626..69258700 26863196 MeRIP-seq:(Medium) rs747073665 Functional Loss DEL dbSNP153 33..35 33 - - - 89310 RMVar_ID_89310 Human_SNP_ID_505563534 m1A Human chr12 - 69258675 69258675 69258675 TCTCCTCGATTAGGAGGCCCAGCTAGAGGAGGAGGCAGAACCTGACCAGGAGGTGGAGGACCTGG TCTCCTCGATTAGGAGGCCCAGCTAGAGGAGGCGGCAGAACCTGACCAGGAGGTGGAGGACCTGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:69258626..69258700 26863196 MeRIP-seq:(Medium) rs962044245 Functional Loss SNV dbSNP153 33..33 33 - - - 89311 RMVar_ID_89311 Human_SNP_ID_505563566 m1A Human chr12 - 69258789 69258789 69258789 GGGCCAGGAGGGGGGCCGTAGCCTGGAACTGGAGGTGGAGGGCCAGGAGGAAGTGGACCCAATGG GGGCCAGGAGGGGGGCCGTAGCCTGGAACTGGGGGTGGAGGGCCAGGAGGAAGTGGACCCAATGG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:69258776..69258800 26863196 MeRIP-seq:(Medium) rs200055894 Functional Loss SNV dbSNP153 33..33 33 - - - 89312 RMVar_ID_89312 Human_SNP_ID_505563579 m1A Human chr12 + 69258831 69258831 69258831 GGCTACGGCCCCCCTCCTGGCCCACCACCTCCACAACAGGGACCACCTCCACCTCCAGGCCCCTT GGCTACGGCCCCCCTCCTGGCCCACCACCTCCCCAACAGGGACCACCTCCACCTCCAGGCCCCTT A C CPSF6 Ensembl:ENSG00000111605 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:69258701..69259025 26863196 MeRIP-seq:(Medium) rs1241584323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228756,Human_RBP_ID_752653,Human_RBP_ID_8382706,Human_RBP_ID_17074919,Human_RBP_ID_17240380,Human_RBP_ID_17355903,Human_RBP_ID_18935560,Human_RBP_ID_25026779,Human_RBP_ID_26911180,Human_RBP_ID_27218072 RMVar_hsa_circ_158146,RMVar_hsa_circ_277579,RMVar_hsa_circ_286191,RMVar_hsa_circ_105735,RMVar_hsa_circ_158148,RMVar_hsa_circ_158147,RMVar_hsa_circ_158145,RMVar_hsa_circ_158150,RMVar_hsa_circ_334555,RMVar_hsa_circ_353172,RMVar_hsa_circ_313813,RMVar_hsa_circ_333036,RMVar_hsa_circ_271894,RMVar_hsa_circ_158151,RMVar_hsa_circ_306002 89313 RMVar_ID_89313 Human_SNP_ID_505563580 m1A Human chr12 + 69258834 69258834 69258834 TACGGCCCCCCTCCTGGCCCACCACCTCCACAACAGGGACCACCTCCACCTCCAGGCCCCTTTCC TACGGCCCCCCTCCTGGCCCACCACCTCCACAGCAGGGACCACCTCCACCTCCAGGCCCCTTTCC A G CPSF6 Ensembl:ENSG00000111605 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:69258651..69259050 26863196 MeRIP-seq:(Medium) rs1413864068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752653,Human_RBP_ID_8382706,Human_RBP_ID_17074919,Human_RBP_ID_17240380,Human_RBP_ID_17355903,Human_RBP_ID_18935560,Human_RBP_ID_25026779,Human_RBP_ID_26911180,Human_RBP_ID_27218072 RMVar_hsa_circ_158146,RMVar_hsa_circ_277579,RMVar_hsa_circ_286191,RMVar_hsa_circ_105735,RMVar_hsa_circ_158148,RMVar_hsa_circ_158147,RMVar_hsa_circ_158145,RMVar_hsa_circ_158150,RMVar_hsa_circ_334555,RMVar_hsa_circ_353172,RMVar_hsa_circ_313813,RMVar_hsa_circ_333036,RMVar_hsa_circ_271894,RMVar_hsa_circ_158151,RMVar_hsa_circ_306002 89314 RMVar_ID_89314 Human_SNP_ID_505587427 m1A Human chr12 + 69359889 69359889 69359889 GGCTAGAAACCCTCCGCCTGGGCCCGCGCGACAGGAGCGCGGTCTCTGAGGGGAGCGGCGACCCC GGCTAGAAACCCTCCGCCTGGGCCCGCGCGACGGGAGCGCGGTCTCTGAGGGGAGCGGCGACCCC A G YEATS4 Ensembl:ENSG00000127337 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:69359800..69359899 32194978 MeRIP-seq:(Medium) rs1218253721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427073,Human_RBP_ID_4246849,Human_RBP_ID_9366635 RMVar_hsa_circ_102659,RMVar_hsa_circ_158166 89315 RMVar_ID_89315 Human_SNP_ID_505590608 m1A Human chr12 - 69371863 69371863 69371863 TGCTCAGAAAGCATTTCCTGACTGACATTTTGATATCAGTATCTAAAACTCCAACCATCTCGTCC TGCTCAGAAAGCATTTCCTGACTGACATTTTGGTATCAGTATCTAAAACTCCAACCATCTCGTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:69371856..69372072 26863196 MeRIP-seq:(Medium) rs1057158293 Functional Loss SNV dbSNP153 33..33 33 - - - 89316 RMVar_ID_89316 Human_SNP_ID_505593608 m1A Human chr12 + 69383776 69383773 69383777 CTTGAAGTGGATAAGAGAACATCAGATAAGATAAATTGGAGACAGACACTGTGGGCAACTCTGTC CTTGAAGTGGATAAGAGAACATCAGATAAG____ATTGGAGACAGACACTGTGGGCAACTCTGTC GATAA G YEATS4 Ensembl:ENSG00000127337 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:69383773..69383941 26863196 MeRIP-seq:(Medium) rs1179971251 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_12021234 RMVar_hsa_circ_158168,RMVar_hsa_circ_102659,RMVar_hsa_circ_124101,RMVar_hsa_circ_158166,RMVar_hsa_circ_81916,RMVar_hsa_circ_158170 89317 RMVar_ID_89317 Human_SNP_ID_505600211 m1A Human chr12 + 69412708 69412708 69412708 ACAAATAAAAATAAAGGCGAGGAAAGTCAAACACTGAGAGAGTTGGCAGCCCAAAGTTGTGCAAT ACAAATAAAAATAAAGGCGAGGAAAGTCAAACGCTGAGAGAGTTGGCAGCCCAAAGTTGTGCAAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:69412670..69413031 26863196 MeRIP-seq:(Medium) rs1200967618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6215274,Human_RBP_ID_12021465 89318 RMVar_ID_89318 Human_SNP_ID_505642619 m1A Human chr12 - 69585501 69585501 69585501 CAGGCTCACCATGGTTCCGAGGAGTTCCGCACACAAGTGAATCCCCTCACAGCTCGTGCTCGGGA CAGGCTCACCATGGTTCCGAGGAGTTCCGCACCCAAGTGAATCCCCTCACAGCTCGTGCTCGGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:69585451..69585576 26863196 MeRIP-seq:(Medium) rs1031515524 Functional Loss SNV dbSNP153 33..33 33 - - - 89319 RMVar_ID_89319 Human_SNP_ID_505642630 m1A Human chr12 - 69585514 69585514 69585514 GAGGCAGGGGAGTCAGGCTCACCATGGTTCCGAGGAGTTCCGCACACAAGTGAATCCCCTCACAG GAGGCAGGGGAGTCAGGCTCACCATGGTTCCGTGGAGTTCCGCACACAAGTGAATCCCCTCACAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:69585451..69585584 26863196 MeRIP-seq:(Medium) rs1390109992 Functional Loss SNV dbSNP153 33..33 33 - - - 89320 RMVar_ID_89320 Human_SNP_ID_505642637 m1A Human chr12 - 69585526 69585526 69585526 GGGGTAGGGCAAGAGGCAGGGGAGTCAGGCTCACCATGGTTCCGAGGAGTTCCGCACACAAGTGA GGGGTAGGGCAAGAGGCAGGGGAGTCAGGCTCGCCATGGTTCCGAGGAGTTCCGCACACAAGTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69585482..69585723 32194978 MeRIP-seq:(Medium) rs111365352 Functional Loss SNV dbSNP153 33..33 33 - - - 89321 RMVar_ID_89321 Human_SNP_ID_505642928 m1A Human chr12 - 69586284 69586284 69586284 TCAGCTCCTGCCTTAAAGATGTTAACAGGTGCAAGGGAAAGGGACGCCTGAAAAGGAAAACCAAG TCAGCTCCTGCCTTAAAGATGTTAACAGGTGCGAGGGAAAGGGACGCCTGAAAAGGAAAACCAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69586280..69586838 32194978 MeRIP-seq:(Medium) rs1320497230 Functional Loss SNV dbSNP153 33..33 33 - - - 89322 RMVar_ID_89322 Human_SNP_ID_505642940 m1A Human chr12 + 69586320 69586317 69586320 CCTGTTAACATCTTTAAGGCAGGAGCTGATGAAGAGAGAGCAGAGACAGCTCGTCTGGTAAGCCT CCTGTTAACATCTTTAAGGCAGGAGCTGAT___GAGAGAGCAGAGACAGCTCGTCTGGTAAGCCT TGAA T CCT2 Ensembl:ENSG00000166226 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:69586239..69586386 26863196 MeRIP-seq:(Medium) rs776742327 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_753982,Human_RBP_ID_810804,Human_RBP_ID_876915,Human_RBP_ID_1477064,Human_RBP_ID_1800670,Human_RBP_ID_3941983,Human_RBP_ID_4246853,Human_RBP_ID_5349923,Human_RBP_ID_18977611,Human_RBP_ID_22437923,Human_RBP_ID_25000252,Human_RBP_ID_26911328 Human_Splice_Rec_1396780,Human_Splice_Rec_1396781,Human_Splice_Rec_1396788,Human_Splice_Rec_1396789,Human_Splice_Rec_1396792,Human_Splice_Rec_1396793,Human_Splice_Rec_1396798,Human_Splice_Rec_1396799,Human_Splice_Rec_1396808,Human_Splice_Rec_1396809,Human_Splice_Rec_1396820,Human_Splice_Rec_1396821,Human_Splice_Rec_1396852,Human_Splice_Rec_1396853,Human_Splice_Rec_1396856,Human_Splice_Rec_1396857,Human_Splice_Rec_1396884,Human_Splice_Rec_1396885,Human_Splice_Rec_1396912,Human_Splice_Rec_1396913 RMVar_hsa_circ_11638,RMVar_hsa_circ_113475,RMVar_hsa_circ_158187,RMVar_hsa_circ_82498,RMVar_hsa_circ_158186 89323 RMVar_ID_89323 Human_SNP_ID_505643344 m1A Human chr12 + 69587565 69587565 69587565 ATGCCTCTCTTATGGTAACCAATGATGGTGCCACTATTCTAAAAAACATTGGTGTTGACAATCCA ATGCCTCTCTTATGGTAACCAATGATGGTGCCGCTATTCTAAAAAACATTGGTGTTGACAATCCA A G CCT2 Ensembl:ENSG00000166226 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69587135..69587642 32194978 MeRIP-seq:(Medium) rs1369534449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35197,Human_RBP_ID_994323,Human_RBP_ID_1477067,Human_RBP_ID_1800677,Human_RBP_ID_3943304,Human_RBP_ID_9020719,Human_RBP_ID_17685260,Human_RBP_ID_17826021,Human_RBP_ID_18263771,Human_RBP_ID_18975974,Human_RBP_ID_23572853,Human_RBP_ID_27218200,Human_RBP_ID_27632898 Human_Splice_Rec_1396784,Human_Splice_Rec_1396785,Human_Splice_Rec_1396796,Human_Splice_Rec_1396802,Human_Splice_Rec_1396803,Human_Splice_Rec_1396812,Human_Splice_Rec_1396813,Human_Splice_Rec_1396824,Human_Splice_Rec_1396825,Human_Splice_Rec_1396860,Human_Splice_Rec_1396861,Human_Splice_Rec_1396888,Human_Splice_Rec_1396889,Human_Splice_Rec_1396916,Human_Splice_Rec_1396917 RMVar_hsa_circ_113475,RMVar_hsa_circ_158187,RMVar_hsa_circ_82498,RMVar_hsa_circ_158186,RMVar_hsa_circ_105955,RMVar_hsa_circ_297171,RMVar_hsa_circ_369386,RMVar_hsa_circ_158188,RMVar_hsa_circ_158189 89324 RMVar_ID_89324 Human_SNP_ID_505646183 m1A Human chr12 + 69597183 69597183 69597183 TATAGGTGGTGAAATTGCCTCTACCTTTGATCACCCAGAACTGGTGAAGCTTGGAAGTTGCAAAC TATAGGTGGTGAAATTGCCTCTACCTTTGATCGCCCAGAACTGGTGAAGCTTGGAAGTTGCAAAC A G CCT2 Ensembl:ENSG00000166226 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69593539..69597182 32194978 MeRIP-seq:(Medium) rs1252856194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35207,Human_RBP_ID_427211,Human_RBP_ID_876922,Human_RBP_ID_1358504,Human_RBP_ID_1477093,Human_RBP_ID_1800715,Human_RBP_ID_4240108,Human_RBP_ID_6216215,Human_RBP_ID_8785167,Human_RBP_ID_18632847,Human_RBP_ID_22436060,Human_RBP_ID_22756069,Human_RBP_ID_23572890 Human_Splice_Rec_1396838,Human_Splice_Rec_1396839,Human_Splice_Rec_1396874,Human_Splice_Rec_1396875,Human_Splice_Rec_1396902,Human_Splice_Rec_1396903,Human_Splice_Rec_1396930,Human_Splice_Rec_1396931,Human_Splice_Rec_1396952 RMVar_hsa_circ_113475,RMVar_hsa_circ_158186,RMVar_hsa_circ_8234,RMVar_hsa_circ_80998,RMVar_hsa_circ_114979,RMVar_hsa_circ_40772,RMVar_hsa_circ_158191,RMVar_hsa_circ_349898,RMVar_hsa_circ_158195,RMVar_hsa_circ_41931,RMVar_hsa_circ_158196,RMVar_hsa_circ_365359,RMVar_hsa_circ_158199,RMVar_hsa_circ_377847 89325 RMVar_ID_89325 Human_SNP_ID_505646435 m1A Human chr12 - 69598070 69598070 69598070 AAGTTCGGATCTCTCATTTTGATTAACTTACCATTCTCAGTGCTTTAGCATAAGACTCCATTGCA AAGTTCGGATCTCTCATTTTGATTAACTTACCGTTCTCAGTGCTTTAGCATAAGACTCCATTGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69598042..69599783 32194978 MeRIP-seq:(Medium) rs926983844 Functional Loss SNV dbSNP153 33..33 33 - - - 89326 RMVar_ID_89326 Human_SNP_ID_505646523 m1A Human chr12 + 69598344 69598344 69598344 ATTTTCATAGTTGCCAACCATCATAGCTGACAATGCAGGCTATGACAGTGCAGACCTGGTGGCAC ATTTTCATAGTTGCCAACCATCATAGCTGACAGTGCAGGCTATGACAGTGCAGACCTGGTGGCAC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs937030002 Functional Loss SNV dbSNP153 33..33 33 - - - 89327 RMVar_ID_89327 Human_SNP_ID_505646918 m1A Human chr12 - 69599915 69599914 69599915 GCACTCAGAAGAACCTGTCGCTTCACTTGAAAACTTTCTGTTATACCCAGGATAGCCATATCTCC GCACTCAGAAGAACCTGTCGCTTCACTTGAAA_CTTTCTGTTATACCCAGGATAGCCATATCTCC GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:69599823..69599971 26863196 MeRIP-seq:(Medium) rs1230533268 Functional Loss DEL dbSNP153 33..33 33 - - - 89328 RMVar_ID_89328 Human_SNP_ID_505646919 m1A Human chr12 - 69599915 69599915 69599915 GCACTCAGAAGAACCTGTCGCTTCACTTGAAAACTTTCTGTTATACCCAGGATAGCCATATCTCC GCACTCAGAAGAACCTGTCGCTTCACTTGAAAGCTTTCTGTTATACCCAGGATAGCCATATCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:69599823..69599971 26863196 MeRIP-seq:(Medium) rs1021044006 Functional Loss SNV dbSNP153 33..33 33 - - - 89329 RMVar_ID_89329 Human_SNP_ID_505646923 m1A Human chr12 + 69599926 69599926 69599926 TATCCTGGGTATAACAGAAAGTTTTCAAGTGAAGCGACAGGTTCTTCTGAGTGCAGCTGAAGCAG TATCCTGGGTATAACAGAAAGTTTTCAAGTGAGGCGACAGGTTCTTCTGAGTGCAGCTGAAGCAG A G CCT2 Ensembl:ENSG00000166226 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69599851..69601471 32194978 MeRIP-seq:(Medium) rs1410487307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427219,Human_RBP_ID_994330,Human_RBP_ID_1477105,Human_RBP_ID_1800728,Human_RBP_ID_3413251,Human_RBP_ID_4240132,Human_RBP_ID_5555678,Human_RBP_ID_6216245,Human_RBP_ID_8785175,Human_RBP_ID_9020737,Human_RBP_ID_17355991,Human_RBP_ID_22795332,Human_RBP_ID_23572902,Human_RBP_ID_26419567,Human_RBP_ID_27218223,Human_RBP_ID_27632926 Human_Splice_Rec_1396846,Human_Splice_Rec_1396847,Human_Splice_Rec_1396908,Human_Splice_Rec_1396909,Human_Splice_Rec_1396938,Human_Splice_Rec_1396939,Human_Splice_Rec_1396953 RMVar_hsa_circ_114979,RMVar_hsa_circ_158191,RMVar_hsa_circ_349898,RMVar_hsa_circ_158196,RMVar_hsa_circ_111286,RMVar_hsa_circ_158201 89330 RMVar_ID_89330 Human_SNP_ID_505679704 m1A Human chr12 + 69738928 69738928 69738928 CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGAAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGCAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG A C RAB3IP Ensembl:ENSG00000127328 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs957503756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247650,Human_RBP_ID_5274146 89331 RMVar_ID_89331 Human_SNP_ID_505679705 m1A Human chr12 + 69738928 69738928 69738928 CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGAAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGGAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG A G RAB3IP Ensembl:ENSG00000127328 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs957503756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247650,Human_RBP_ID_5274146 89332 RMVar_ID_89332 Human_SNP_ID_505679706 m1A Human chr12 + 69738928 69738928 69738928 CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGAAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG CGTAGTGAGCCCGCCGCCGTGGAGTGTAGCGGTAAGGGCTCGCCGTCCTCCTCCGTTTCTCGCTG A T RAB3IP Ensembl:ENSG00000127328 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs957503756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247650,Human_RBP_ID_5274146 89333 RMVar_ID_89333 Human_SNP_ID_505699929 m1A Human chr12 + 69815694 69815694 69815694 AGTGAATGTAATTTATAGTTGCCAAAAAAAAAAAAAACCTGAAATAAATAAATGTTAGATTGAAT AGTGAATGTAATTTATAGTTGCCAAAAAAAAACAAAACCTGAAATAAATAAATGTTAGATTGAAT A C AC025263.2,RAB3IP Ensembl:ENSG00000258052,Ensembl:ENSG00000127328 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs76965682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427264,Human_RBP_ID_3413326,Human_RBP_ID_26419582 RMVar_hsa_circ_89689,RMVar_hsa_circ_158214 89334 RMVar_ID_89334 Human_SNP_ID_505700689 m1A Human chr12 + 69818842 69818842 69818842 TACCTCTGGAGAGGTAGAGGAGGAGCAAATCTATGAGTAAGTCACTGGTAATGTTTTAGTCCCTG TACCTCTGGAGAGGTAGAGGAGGAGCAAATCTGTGAGTAAGTCACTGGTAATGTTTTAGTCCCTG A G AC025263.2,RAB3IP Ensembl:ENSG00000258052,Ensembl:ENSG00000127328 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:69818794..69818958 26863196 MeRIP-seq:(Medium) rs972564752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6216486 RMVar_hsa_circ_89689,RMVar_hsa_circ_158214 89335 RMVar_ID_89335 Human_SNP_ID_169108192 m1A Human chr3 + 195078746 195078746 195078746 TCCCCAGTCCCCAGGGCTGCACACAGCCCCCCACACTTCCAGAGCTGTCCTCCCCACCTCCCATC TCCCCAGTCCCCAGGGCTGCACACAGCCCCCCTCACTTCCAGAGCTGTCCTCCCCACCTCCCATC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195078743..195079055 26863196 MeRIP-seq:(Medium) rs1038768621 Functional Loss SNV dbSNP153 33..33 33 - - - 89336 RMVar_ID_89336 Human_SNP_ID_169108216 m1A Human chr3 + 195078837 195078837 195078837 TCGCCGCCTGGGATCCCCTTCCTCTCTGCTCCATCCCTAGGGACACCCTCAAGAATTCCAAATGC TCGCCGCCTGGGATCCCCTTCCTCTCTGCTCCGTCCCTAGGGACACCCTCAAGAATTCCAAATGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:195078833..195079018 26863196 MeRIP-seq:(Medium) rs1002037302 Functional Loss SNV dbSNP153 33..33 33 - - - 89337 RMVar_ID_89337 Human_SNP_ID_169149706 m1A Human chr3 - 195238312 195238312 195238312 GAGGCTGTGGGAAGGCTGGAGGGGAGGATTGGAAAACTGGATAGGATCTTACCAGGCAGATGGGG GAGGCTGTGGGAAGGCTGGAGGGGAGGATTGGCAAACTGGATAGGATCTTACCAGGCAGATGGGG T G XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195238262..195238391 26863196 MeRIP-seq:(Medium) rs1296317304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_109445,RMVar_hsa_circ_223770 89338 RMVar_ID_89338 Human_SNP_ID_169150468 m1A Human chr3 - 195241697 195241683 195241698 ACTGATACCTGAATGGCTAGAAGGATTCAGGCAGAAGGTTCTGGGGGAGGGTTCTCTGAGCAGAG ACTGATACCTGAATGGCTAGAAGGATTCAGG_______________GAGGGTTCTCTGAGCAGAG CCCCCAGAACCTTCTG C XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195241682..195241769 26863196 MeRIP-seq:(Medium) rs919747601 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_109445,RMVar_hsa_circ_223770 89339 RMVar_ID_89339 Human_SNP_ID_169150472 m1A Human chr3 - 195241697 195241697 195241697 ACTGATACCTGAATGGCTAGAAGGATTCAGGCAGAAGGTTCTGGGGGAGGGTTCTCTGAGCAGAG ACTGATACCTGAATGGCTAGAAGGATTCAGGCGGAAGGTTCTGGGGGAGGGTTCTCTGAGCAGAG T C XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195241682..195241769 26863196 MeRIP-seq:(Medium) rs1236612572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_109445,RMVar_hsa_circ_223770 89340 RMVar_ID_89340 Human_SNP_ID_169151030 m1A Human chr3 - 195243986 195243986 195243986 GACAGCGTGGGGAGGAGGGGCTGTCACTTTTGAACTGTCAGTAAAGTAGGTTGTGAGAATGGATA GACAGCGTGGGGAGGAGGGGCTGTCACTTTTGTACTGTCAGTAAAGTAGGTTGTGAGAATGGATA T A XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195243983..195244049 26863196 MeRIP-seq:(Medium) rs1231230260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_109445,RMVar_hsa_circ_223770 89341 RMVar_ID_89341 Human_SNP_ID_169152682 m1A Human chr3 + 195249858 195249858 195249858 TAAACTCTAGTGGAGAAAACCTCAACATCCCAACCTAGTAGCGGCCCTTTCCTGATGGATCCAGA TAAACTCTAGTGGAGAAAACCTCAACATCCCAGCCTAGTAGCGGCCCTTTCCTGATGGATCCAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:195249853..195250166;chr3:195249844..195249992 26863196 MeRIP-seq:(Medium) rs183658419 Functional Loss SNV dbSNP153 33..33 33 - - - 89342 RMVar_ID_89342 Human_SNP_ID_169174565 m1A Human chr3 - 195337964 195337936 195337964 CAGTGCAAAGGCATTGAGGTGGGAGTGGCCCCAGGCTCAGGTTGAGGTGGGAGTGGCCCCGGGCT CAGTGCAAAGGCATTGAGGTGGGAGTGGCCCC____________________________GGGCT CGGGGCCACTCCCACCTCAACCTGAGCCT C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195337744..195338026 26863196 MeRIP-seq:(Medium) rs1184232429 Functional Loss DEL dbSNP153 33..60 33 - - - Human_RBP_ID_7175025 RMVar_hsa_circ_325798,RMVar_hsa_circ_32736,RMVar_hsa_circ_104683,RMVar_hsa_circ_358200,RMVar_hsa_circ_26703,RMVar_hsa_circ_223789,RMVar_hsa_circ_351127,RMVar_hsa_circ_65820,RMVar_hsa_circ_38454,RMVar_hsa_circ_223796,RMVar_hsa_circ_316364,RMVar_hsa_circ_347646,RMVar_hsa_circ_309040,RMVar_hsa_circ_223798,RMVar_hsa_circ_223799,RMVar_hsa_circ_223797,RMVar_hsa_circ_12481,RMVar_hsa_circ_223803,RMVar_hsa_circ_297489,RMVar_hsa_circ_312573,RMVar_hsa_circ_223804,RMVar_hsa_circ_358116,RMVar_hsa_circ_299838,RMVar_hsa_circ_223805,RMVar_hsa_circ_223806,RMVar_hsa_circ_223807,RMVar_hsa_circ_64213,RMVar_hsa_circ_332519 89343 RMVar_ID_89343 Human_SNP_ID_169174572 m1A Human chr3 - 195337964 195337964 195337964 CAGTGCAAAGGCATTGAGGTGGGAGTGGCCCCAGGCTCAGGTTGAGGTGGGAGTGGCCCCGGGCT CAGTGCAAAGGCATTGAGGTGGGAGTGGCCCCGGGCTCAGGTTGAGGTGGGAGTGGCCCCGGGCT T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195337744..195338026 26863196 MeRIP-seq:(Medium) rs113179685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7175025 GWAS_ID_11594,GWAS_ID_11595,GWAS_ID_11596,GWAS_ID_11597,GWAS_ID_11598,GWAS_ID_11599,GWAS_ID_11600,GWAS_ID_11601,GWAS_ID_11602,GWAS_ID_11603,GWAS_ID_11604,GWAS_ID_11605,GWAS_ID_11606,GWAS_ID_11607,GWAS_ID_11608,GWAS_ID_11609,GWAS_ID_11610,GWAS_ID_11611,GWAS_ID_11612,GWAS_ID_11613,GWAS_ID_11614,GWAS_ID_11615,GWAS_ID_11616,GWAS_ID_11617,GWAS_ID_11618,GWAS_ID_11619,GWAS_ID_11620,GWAS_ID_11621,GWAS_ID_11622,GWAS_ID_11623,GWAS_ID_11624,GWAS_ID_11625,GWAS_ID_11626,GWAS_ID_11627,GWAS_ID_11628,GWAS_ID_11629,GWAS_ID_11630,GWAS_ID_11631,GWAS_ID_11632,GWAS_ID_11633,GWAS_ID_11634,GWAS_ID_11635,GWAS_ID_11636,GWAS_ID_11637,GWAS_ID_11638,GWAS_ID_11639,GWAS_ID_11640,GWAS_ID_11641,GWAS_ID_11642,GWAS_ID_11643,GWAS_ID_11644 RMVar_hsa_circ_325798,RMVar_hsa_circ_32736,RMVar_hsa_circ_104683,RMVar_hsa_circ_358200,RMVar_hsa_circ_26703,RMVar_hsa_circ_223789,RMVar_hsa_circ_351127,RMVar_hsa_circ_65820,RMVar_hsa_circ_38454,RMVar_hsa_circ_223796,RMVar_hsa_circ_316364,RMVar_hsa_circ_347646,RMVar_hsa_circ_309040,RMVar_hsa_circ_223798,RMVar_hsa_circ_223799,RMVar_hsa_circ_223797,RMVar_hsa_circ_12481,RMVar_hsa_circ_223803,RMVar_hsa_circ_297489,RMVar_hsa_circ_312573,RMVar_hsa_circ_223804,RMVar_hsa_circ_358116,RMVar_hsa_circ_299838,RMVar_hsa_circ_223805,RMVar_hsa_circ_223806,RMVar_hsa_circ_223807,RMVar_hsa_circ_64213,RMVar_hsa_circ_332519 89344 RMVar_ID_89344 Human_SNP_ID_169196090 m1A Human chr3 - 195426113 195426113 195426113 AAGAGGAAGGGATGGTTAAGAATTAAGATCAGAGGTAGGCAAGGATGAGGTCATGTTAGGCATTA AAGAGGAAGGGATGGTTAAGAATTAAGATCAGGGGTAGGCAAGGATGAGGTCATGTTAGGCATTA T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195426111..195426292 26863196 MeRIP-seq:(Medium) rs959437378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789,RMVar_hsa_circ_223816 89345 RMVar_ID_89345 Human_SNP_ID_169251857 m1A Human chr3 + 195523784 195523784 195523784 GATACTTTGGCTCCAAGCCTTCAGCTGCAGCTAATCTATGCAACAATCATGTACAAAGAAATTAA GATACTTTGGCTCCAAGCCTTCAGCTGCAGCTCATCTATGCAACAATCATGTACAAAGAAATTAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:195523743..195523820 26863196 MeRIP-seq:(Medium) rs756904324 Functional Loss SNV dbSNP153 33..33 33 - - - 89346 RMVar_ID_89346 Human_SNP_ID_169256692 m1A Human chr3 - 195542995 195542995 195542995 CAATGGCGGCCTCGACGGCCTCGCACCGGCCCATCAAGGGGATCTTGAAGAACAAGACCTCTACG CAATGGCGGCCTCGACGGCCTCGCACCGGCCCGTCAAGGGGATCTTGAAGAACAAGACCTCTACG T C PPP1R2 Ensembl:ENSG00000184203 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:195542976..195543000 26863196 MeRIP-seq:(Medium) rs781522597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26825199 Human_Splice_Rec_527581,Human_Splice_Rec_527599,Human_Splice_Rec_527607,Human_Splice_Rec_527617,Human_Splice_Rec_527621 89347 RMVar_ID_89347 Human_SNP_ID_169256710 m1A Human chr3 + 195543024 195543024 195543024 TGATGGGCCGGTGCGAGGCCGTCGAGGCCGCCATTGCCGGGCGCTCCGGCTGTCGGCTCAGGGTC TGATGGGCCGGTGCGAGGCCGTCGAGGCCGCCCTTGCCGGGCGCTCCGGCTGTCGGCTCAGGGTC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:195542976..195543025 26863196 MeRIP-seq:(Medium) rs1275852524 Functional Loss SNV dbSNP153 33..33 33 - - - 89348 RMVar_ID_89348 Human_SNP_ID_169256725 m1A Human chr3 - 195543044 195543044 195543044 CGGACCCCACGCCAAGCAGCGACCCTGAGCCGACAGCCGGAGCGCCCGGCAATGGCGGCCTCGAC CGGACCCCACGCCAAGCAGCGACCCTGAGCCGGCAGCCGGAGCGCCCGGCAATGGCGGCCTCGAC T C PPP1R2 Ensembl:ENSG00000184203 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr3:195543006..195543325;chr3:195542926..195543285 26863196 MeRIP-seq:(Medium) rs977092332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_938848,Human_RBP_ID_4736086,Human_RBP_ID_26824379 89349 RMVar_ID_89349 Human_SNP_ID_169256730 m1A Human chr3 - 195543049 195543049 195543049 CTTCGCGGACCCCACGCCAAGCAGCGACCCTGAGCCGACAGCCGGAGCGCCCGGCAATGGCGGCC CTTCGCGGACCCCACGCCAAGCAGCGACCCTGGGCCGACAGCCGGAGCGCCCGGCAATGGCGGCC T C PPP1R2 Ensembl:ENSG00000184203 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:195542967..195543325 26863196 MeRIP-seq:(Medium) rs1422068965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758662,Human_RBP_ID_26824379 Human_miRNA_ID_2268707 89350 RMVar_ID_89350 Human_SNP_ID_169286595 m1A Human chr3 - 195648237 195648237 195648237 GCACGGCCCTCAAACTGGAACATCAGCTCCCCACCAGGTCTCCAGCCGCACGGCCCTCATACTGG GCACGGCCCTCAAACTGGAACATCAGCTCCCCGCCAGGTCTCCAGCCGCACGGCCCTCATACTGG T C LOC105374297,LOC105374297:2,LOC105374297:3,LOC105374297:4 RNACentral:URS00008C1C5D,RNACentral:URS0000A77230,RNACentral:URS00008C369E,RNACentral:URS0000A76EF3 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195648107..195648262 26863196 MeRIP-seq:(Medium) rs1299298837 Functional Loss SNV dbSNP153 33..33 33 - - - 89351 RMVar_ID_89351 Human_SNP_ID_169290408 m1A Human chr3 - 195658143 195658143 195658143 AGGGACTCACCGCCTTGGCCAGCGCCAGCGCCAAGCGCCGAGCGCTTGGCAACCGCGACAGGCCC AGGGACTCACCGCCTTGGCCAGCGCCAGCGCCGAGCGCCGAGCGCTTGGCAACCGCGACAGGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195658125..195658289 26863196 MeRIP-seq:(Medium) rs1247984057 Functional Loss SNV dbSNP153 33..33 33 - - - 89352 RMVar_ID_89352 Human_SNP_ID_169299355 m1A Human chr3 - 195683842 195683842 195683842 CACACTGACCTTCCCAGTGCCGACGTCCACATAGGACAGGGTGTGCTTCCTCCAGTGCACCTCAA CACACTGACCTTCCCAGTGCCGACGTCCACATGGGACAGGGTGTGCTTCCTCCAGTGCACCTCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:195681622..195685904 32194978 MeRIP-seq:(Medium) rs1275898904 Functional Loss SNV dbSNP153 33..33 33 - - - 89353 RMVar_ID_89353 Human_SNP_ID_169300920 m1A Human chr3 - 195687357 195687357 195687357 AGGGGGCGGAGCTCACACAGTAATGCTCTGGCAGGGGGCGGAGCTCACACAGTAATGCTGACGGG AGGGGGCGGAGCTCACACAGTAATGCTCTGGCGGGGGGCGGAGCTCACACAGTAATGCTGACGGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:195687343..195687594 26863196 MeRIP-seq:(Medium) rs1247609225 Functional Loss SNV dbSNP153 33..33 33 - - - 89354 RMVar_ID_89354 Human_SNP_ID_169300921 m1A Human chr3 - 195687357 195687357 195687357 AGGGGGCGGAGCTCACACAGTAATGCTCTGGCAGGGGGCGGAGCTCACACAGTAATGCTGACGGG AGGGGGCGGAGCTCACACAGTAATGCTCTGGCCGGGGGCGGAGCTCACACAGTAATGCTGACGGG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:195687343..195687594 26863196 MeRIP-seq:(Medium) rs1247609225 Functional Loss SNV dbSNP153 33..33 33 - - - 89355 RMVar_ID_89355 Human_SNP_ID_169310007 m1A Human chr3 + 195710400 195710400 195710400 CTGGCTCCTGGTGAGTGAGTTAATTGAGATCCATTAGGGAGGGACCTGGCTCCTGGCGAGTGAGT CTGGCTCCTGGTGAGTGAGTTAATTGAGATCCGTTAGGGAGGGACCTGGCTCCTGGCGAGTGAGT A G SMBD1P,MUC20-OT1 Ensembl:ENSG00000283426,Ensembl:ENSG00000242086 Pseudogene,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195710255..195710425 26863196 MeRIP-seq:(Medium) rs1320108656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18927102 RMVar_hsa_circ_66898 89356 RMVar_ID_89356 Human_SNP_ID_169310355 m1A Human chr3 + 195711037 195711037 195711037 CTGGTGAGTGAGTTAATTGAGATGAGGTGTGGAGGGACCTGGCTCCTGGTGAGTGAGTTAATTGA CTGGTGAGTGAGTTAATTGAGATGAGGTGTGGGGGGACCTGGCTCCTGGTGAGTGAGTTAATTGA A G SMBD1P,MUC20-OT1 Ensembl:ENSG00000283426,Ensembl:ENSG00000242086 Pseudogene,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195710981..195711058 26863196 MeRIP-seq:(Medium) rs897959659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834331,Human_RBP_ID_9147242,Human_RBP_ID_17152367,Human_RBP_ID_18927132 RMVar_hsa_circ_66898 89357 RMVar_ID_89357 Human_SNP_ID_169373815 m1A Human chr3 - 195863797 195863797 195863797 CTGGGTGACAGACTGGGAGGAAACCAGGCTGGACCTGGGCAGGCGGGATGTGTTGGCCACAGGGA CTGGGTGACAGACTGGGAGGAAACCAGGCTGGTCCTGGGCAGGCGGGATGTGTTGGCCACAGGGA T A TNK2 Ensembl:ENSG00000061938 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195863748..195863912 26863196 MeRIP-seq:(Medium) rs1256170509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530767,Human_RBP_ID_26510709 RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89358 RMVar_ID_89358 Human_SNP_ID_169373816 m1A Human chr3 - 195863797 195863797 195863797 CTGGGTGACAGACTGGGAGGAAACCAGGCTGGACCTGGGCAGGCGGGATGTGTTGGCCACAGGGA CTGGGTGACAGACTGGGAGGAAACCAGGCTGGGCCTGGGCAGGCGGGATGTGTTGGCCACAGGGA T C TNK2 Ensembl:ENSG00000061938 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195863748..195863912 26863196 MeRIP-seq:(Medium) rs1256170509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530767,Human_RBP_ID_26510709 RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89359 RMVar_ID_89359 Human_SNP_ID_169373817 m1A Human chr3 - 195863812 195863812 195863812 CCCCCAGGCCCTGCCCTGGGTGACAGACTGGGAGGAAACCAGGCTGGACCTGGGCAGGCGGGATG CCCCCAGGCCCTGCCCTGGGTGACAGACTGGGGGGAAACCAGGCTGGACCTGGGCAGGCGGGATG T C TNK2 Ensembl:ENSG00000061938 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:195863762..195866962 26863196 MeRIP-seq:(Medium) rs746976374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5530767,Human_RBP_ID_18002416,Human_RBP_ID_26510709 RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89360 RMVar_ID_89360 Human_SNP_ID_169373885 m1A Human chr3 - 195864012 195864012 195864012 GGCTGCGGGAGGCTGGGAGCCCTGCCCTGCCCATCCCTCCTGCACCAGCGCTGTCCCTGCACACT GGCTGCGGGAGGCTGGGAGCCCTGCCCTGCCCGTCCCTCCTGCACCAGCGCTGTCCCTGCACACT T C TNK2 Ensembl:ENSG00000061938 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195863961..195864062 26863196 MeRIP-seq:(Medium) rs1443105040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27500619 RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89361 RMVar_ID_89361 Human_SNP_ID_169374957 m1A Human chr3 - 195866944 195866944 195866944 AGTGCCACAAAGTGCTGGAGATGTTCGACTGGAACCTGGAGCAGGCCGGCTGCCACCTTCTGGGC AGTGCCACAAAGTGCTGGAGATGTTCGACTGGGACCTGGAGCAGGCCGGCTGCCACCTTCTGGGC T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195864161..195866978 26863196 MeRIP-seq:(Medium) rs1490261283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_529388,Human_Splice_Rec_529389,Human_Splice_Rec_529416,Human_Splice_Rec_529417,Human_Splice_Rec_529444,Human_Splice_Rec_529445,Human_Splice_Rec_529474,Human_Splice_Rec_529475,Human_Splice_Rec_529502,Human_Splice_Rec_529503,Human_Splice_Rec_529528,Human_Splice_Rec_529529,Human_Splice_Rec_529556,Human_Splice_Rec_529557,Human_Splice_Rec_529562,Human_Splice_Rec_529563,Human_Splice_Rec_529588,Human_Splice_Rec_529589,Human_Splice_Rec_529616,Human_Splice_Rec_529617 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89362 RMVar_ID_89362 Human_SNP_ID_169375108 m1A Human chr3 - 195867212 195867212 195867212 GGTGACCACAGAGGAGTGCCAGGCGGCCCTGCAGTGCCACGGCTGGAGCGTGCAGAGGGCTGCCC GGTGACCACAGAGGAGTGCCAGGCGGCCCTGCGGTGCCACGGCTGGAGCGTGCAGAGGGCTGCCC T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195867011..195867493 26863196 MeRIP-seq:(Medium) rs771593431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19013378 Human_Splice_Rec_529386,Human_Splice_Rec_529387,Human_Splice_Rec_529414,Human_Splice_Rec_529415,Human_Splice_Rec_529472,Human_Splice_Rec_529473,Human_Splice_Rec_529500,Human_Splice_Rec_529501,Human_Splice_Rec_529554,Human_Splice_Rec_529555,Human_Splice_Rec_529560,Human_Splice_Rec_529561 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89363 RMVar_ID_89363 Human_SNP_ID_169375383 m1A Human chr3 - 195867650 195867650 195867650 CCACTATTACTTGCTGCCCGAGCGACCATCCTACCTGGAGCGCTACCAGCGCTTCCTGCGTGAGG CCACTATTACTTGCTGCCCGAGCGACCATCCTGCCTGGAGCGCTACCAGCGCTTCCTGCGTGAGG T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195867599..195868157 26863196 MeRIP-seq:(Medium) rs1298821975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26825201 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89364 RMVar_ID_89364 Human_SNP_ID_169375392 m1A Human chr3 - 195867662 195867662 195867662 GGTCAGCAGCACCCACTATTACTTGCTGCCCGAGCGACCATCCTACCTGGAGCGCTACCAGCGCT GGTCAGCAGCACCCACTATTACTTGCTGCCCGGGCGACCATCCTACCTGGAGCGCTACCAGCGCT T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:195867546..195867700 26863196 MeRIP-seq:(Medium) rs778020093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4736130,Human_RBP_ID_26825201 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89365 RMVar_ID_89365 Human_SNP_ID_169375542 m1A Human chr3 + 195867920 195867908 195867920 AGCCTTGAGGGGACAGGGGCTCCCGCGGAGGCACCCGGGGAGGGGAAGCAGGTCCAGGCCACTGG AGCCTTGAGGGGACAGGGGCT____________CCCGGGGAGGGGAAGCAGGTCCAGGCCACTGG TCCCGCGGAGGCA T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:195867872..195868022;chr3:195867767..195867980 26863196 MeRIP-seq:(Medium) rs1300788954 Functional Loss DEL dbSNP153 22..33 33 - - - 89366 RMVar_ID_89366 Human_SNP_ID_169375554 m1A Human chr3 + 195867916 195867916 195867916 CTCGAGCCTTGAGGGGACAGGGGCTCCCGCGGAGGCACCCGGGGAGGGGAAGCAGGTCCAGGCCA CTCGAGCCTTGAGGGGACAGGGGCTCCCGCGGGGGCACCCGGGGAGGGGAAGCAGGTCCAGGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195867508..195868756 26863196 MeRIP-seq:(Medium) rs780032836 Functional Loss SNV dbSNP153 33..33 33 - - - 89367 RMVar_ID_89367 Human_SNP_ID_169375973 m1A Human chr3 - 195868451 195868451 195868451 GCAGCTGGCCATGGACGCCTGCTCCCTGCTGGACGAGACCCCGCCTCAGAGCCCCACGCGGGCAC GCAGCTGGCCATGGACGCCTGCTCCCTGCTGGGCGAGACCCCGCCTCAGAGCCCCACGCGGGCAC T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195868277..195868627 26863196 MeRIP-seq:(Medium) rs762803119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89368 RMVar_ID_89368 Human_SNP_ID_169376903 m1A Human chr3 - 195870165 195870165 195870165 TGGGAAACCCCATGGACCCCCCCGACCTCCTGAGCGTGGAACTGAGCACCTCCCGGCCCCCCCAG TGGGAAACCCCATGGACCCCCCCGACCTCCTGCGCGTGGAACTGAGCACCTCCCGGCCCCCCCAG T G TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195870081..195870239 26863196 MeRIP-seq:(Medium) rs989818546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3964535 Human_Splice_Rec_529382,Human_Splice_Rec_529383,Human_Splice_Rec_529410,Human_Splice_Rec_529411,Human_Splice_Rec_529438,Human_Splice_Rec_529439,Human_Splice_Rec_529466,Human_Splice_Rec_529467,Human_Splice_Rec_529496,Human_Splice_Rec_529497,Human_Splice_Rec_529524,Human_Splice_Rec_529525,Human_Splice_Rec_529550,Human_Splice_Rec_529551,Human_Splice_Rec_529584,Human_Splice_Rec_529585,Human_Splice_Rec_529610,Human_Splice_Rec_529611,Human_Splice_Rec_529619,Human_Splice_Rec_529642,Human_Splice_Rec_529663,Human_Splice_Rec_529678,Human_Splice_Rec_529687,Human_Splice_Rec_529692,Human_Splice_Rec_529693,Human_Splice_Rec_529696,Human_Splice_Rec_529697,Human_Splice_Rec_529702,Human_Splice_Rec_529703,Human_Splice_Rec_529710,Human_Splice_Rec_529711 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 89369 RMVar_ID_89369 Human_SNP_ID_169381445 m1A Human chr3 - 195881504 195881504 195881504 GGTGTTACAGGGATAGATGCCGTGTCCTCTCCAAGGGGCGTTGCTGGGGGGGGTGTTAGAGGGAC GGTGTTACAGGGATAGATGCCGTGTCCTCTCCGAGGGGCGTTGCTGGGGGGGGTGTTAGAGGGAC T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195881499..195881656 26863196 MeRIP-seq:(Medium) rs1446311057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9435234,Human_RBP_ID_18954052 RMVar_hsa_circ_20195,RMVar_hsa_circ_42948,RMVar_hsa_circ_280698,RMVar_hsa_circ_11259,RMVar_hsa_circ_310424,RMVar_hsa_circ_100106,RMVar_hsa_circ_223832,RMVar_hsa_circ_223831 89370 RMVar_ID_89370 Human_SNP_ID_169382894 m1A Human chr3 - 195885439 195885439 195885439 AGGGCTAAAAATGGACAAGGAGGTGTCTGTGGAGGGCCCCTGCGGCTCCATCGATGCGGGTTAGG AGGGCTAAAAATGGACAAGGAGGTGTCTGTGGGGGGCCCCTGCGGCTCCATCGATGCGGGTTAGG T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195885432..195885559 26863196 MeRIP-seq:(Medium) rs949369435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_529775 RMVar_hsa_circ_20195,RMVar_hsa_circ_280698,RMVar_hsa_circ_11259,RMVar_hsa_circ_100106,RMVar_hsa_circ_223832,RMVar_hsa_circ_223831 89371 RMVar_ID_89371 Human_SNP_ID_169385487 m1A Human chr3 - 195892859 195892859 195892859 TGATTCAGAAAGGTCCTTTTTCAGCCAGTGTCAGAGCTGCTCAGCTGGGGAGGGAGGGAGAGAGG TGATTCAGAAAGGTCCTTTTTCAGCCAGTGTCTGAGCTGCTCAGCTGGGGAGGGAGGGAGAGAGG T A TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195892857..195892976 26863196 MeRIP-seq:(Medium) rs1312513461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 89372 RMVar_ID_89372 Human_SNP_ID_169386008 m1A Human chr3 - 195894598 195894598 195894598 GATCACCTGAGACGAGGACGCTGAGGTCAGGAATTCGGGACCAGCCTGGCCAACATGGCGGAAAA GATCACCTGAGACGAGGACGCTGAGGTCAGGAGTTCGGGACCAGCCTGGCCAACATGGCGGAAAA T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195894592..195894718 26863196 MeRIP-seq:(Medium) rs1469607768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14760405 RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 89373 RMVar_ID_89373 Human_SNP_ID_169386023 m1A Human chr3 + 195894649 195894649 195894649 CGTCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGAGATGACAGGCGTGAGCCACCGCG CGTCTCAGGTGATCTGCCCGCCTCGGCCTCCCGAAGTGCTGAGATGACAGGCGTGAGCCACCGCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195894647..195896206 26863196 MeRIP-seq:(Medium) rs144411046 Functional Loss SNV dbSNP153 33..33 33 - - - 89374 RMVar_ID_89374 Human_SNP_ID_169386329 m1A Human chr3 - 195895416 195895416 195895416 GAGACGCAGTAGCGGCCCTGCACTTCTGGAGGATGCTCGAGGCCCGGCCCCCCAGGACGCAGGGC GAGACGCAGTAGCGGCCCTGCACTTCTGGAGGTTGCTCGAGGCCCGGCCCCCCAGGACGCAGGGC T A TNK2 Ensembl:ENSG00000061938 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:195895411..195895512 32194978 MeRIP-seq:(Medium) rs1373861847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3722362,Human_RBP_ID_8210441,Human_RBP_ID_18169365 RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 89375 RMVar_ID_89375 Human_SNP_ID_169390379 m1A Human chr3 - 195909191 195909191 195909191 GTGGACGGGCTCGGCGGGCTGGCCTGTGGCGCAGGAGGAGGGGCTGGGGCCCCGCGGGCAGCACC GTGGACGGGCTCGGCGGGCTGGCCTGTGGCGCGGGAGGAGGGGCTGGGGCCCCGCGGGCAGCACC T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:195908643..195909314 26863196 MeRIP-seq:(Medium) rs1444755305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266472,Human_RBP_ID_834926,Human_RBP_ID_3721065,Human_RBP_ID_5241651,Human_RBP_ID_5325399,Human_RBP_ID_8124998,Human_RBP_ID_8209563,Human_RBP_ID_8943534,Human_RBP_ID_9334013,Human_RBP_ID_9354357,Human_RBP_ID_9435245,Human_RBP_ID_18169692,Human_RBP_ID_18499931,Human_RBP_ID_18954064,Human_RBP_ID_22481175,Human_RBP_ID_22725671,Human_RBP_ID_26790994 89376 RMVar_ID_89376 Human_SNP_ID_169390502 m1A Human chr3 + 195909518 195909518 195909518 GCCGGGGGCCCCCGACCGGCTCGGCCCAGCGCACTCGCTTGCCCCCCAGAGGCCGCGCGCTCCCA GCCGGGGGCCCCCGACCGGCTCGGCCCAGCGCGCTCGCTTGCCCCCCAGAGGCCGCGCGCTCCCA A G TNK2-AS1 Ensembl:ENSG00000224614 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:195909373..195909756 26863196 MeRIP-seq:(Medium) rs1052047629 Functional Loss SNV dbSNP153 33..33 33 - - - 89377 RMVar_ID_89377 Human_SNP_ID_169404302 m1A Human chr3 + 195954219 195954219 195954219 CGCCCGCGGGGGTCCGGGCAGGGGCGGTGGAGACGGCGGAGGTCGGGGCAGGGGACGGGGGAGGC CGCCCGCGGGGGTCCGGGCAGGGGCGGTGGAGGCGGCGGAGGTCGGGGCAGGGGACGGGGGAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:195954186..195954258 26863196 MeRIP-seq:(Medium) rs867372703 Functional Loss SNV dbSNP153 33..33 33 - - - 89378 RMVar_ID_89378 Human_SNP_ID_169417703 m1A Human chr3 + 195989707 195989707 195989707 CACCCGGCCGAGCCCGGCCACTCCTCGCACCCACCCGGGCGGTTTCACCCGCCCCGCCGGCCCCA CACCCGGCCGAGCCCGGCCACTCCTCGCACCCCCCCGGGCGGTTTCACCCGCCCCGCCGGCCCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:195989705..195989846 26863196 MeRIP-seq:(Medium) rs1209719774 Functional Loss SNV dbSNP153 33..33 33 - - - 89379 RMVar_ID_89379 Human_SNP_ID_169417753 m1A Human chr3 + 195989808 195989808 195989808 ACAGACGGCGGCAGAGGCCCGGCCCAGCCAGGACTCCACCCCGGTGACCCTGGGCAGACACGACT ACAGACGGCGGCAGAGGCCCGGCCCAGCCAGGGCTCCACCCCGGTGACCCTGGGCAGACACGACT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:195989707..195989834 26863196 MeRIP-seq:(Medium) rs1355592828 Functional Loss SNV dbSNP153 33..33 33 - - - 89380 RMVar_ID_89380 Human_SNP_ID_169436418 m1A Human chr3 + 196055464 196055464 196055464 ACCCCAATTCTATCTCATTATCTGCTGCTTTAAGTACATTCTTGCTACTTCTCTCAAGCTAACCT ACCCCAATTCTATCTCATTATCTGCTGCTTTAGGTACATTCTTGCTACTTCTCTCAAGCTAACCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196055427..196055511 26863196 MeRIP-seq:(Medium) rs927957167 Functional Loss SNV dbSNP153 33..33 33 - - - 89381 RMVar_ID_89381 Human_SNP_ID_169442331 m1A Human chr3 - 196075302 196075302 196075302 CCGGTTCAGCCTGGCTCGGCAAGTAGATGGCGATAACAGTCATGTGGAGATGAAACTTGCTGTAG CCGGTTCAGCCTGGCTCGGCAAGTAGATGGCGGTAACAGTCATGTGGAGATGAAACTTGCTGTAG T C TFRC Ensembl:ENSG00000072274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196075251..196075395 26863196 MeRIP-seq:(Medium) rs769447421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66642,Human_RBP_ID_782868,Human_RBP_ID_938254,Human_RBP_ID_2774450,Human_RBP_ID_4756923,Human_RBP_ID_5530770,Human_RBP_ID_5602307,Human_RBP_ID_14761423,Human_RBP_ID_22092912,Human_RBP_ID_22418396,Human_RBP_ID_22456455 Human_Splice_Rec_529928,Human_Splice_Rec_529998,Human_Splice_Rec_530086,Human_Splice_Rec_530094 RMVar_hsa_circ_121595,RMVar_hsa_circ_223843,RMVar_hsa_circ_308948,RMVar_hsa_circ_4933,RMVar_hsa_circ_223854,RMVar_hsa_circ_341777,RMVar_hsa_circ_59092,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223865,RMVar_hsa_circ_223866,RMVar_hsa_circ_223867,RMVar_hsa_circ_329308,RMVar_hsa_circ_35376,RMVar_hsa_circ_297912,RMVar_hsa_circ_115479,RMVar_hsa_circ_223875,RMVar_hsa_circ_70073,RMVar_hsa_circ_325076,RMVar_hsa_circ_48394,RMVar_hsa_circ_223878,RMVar_hsa_circ_98087,RMVar_hsa_circ_279359,RMVar_hsa_circ_315825,RMVar_hsa_circ_223877,RMVar_hsa_circ_287545,RMVar_hsa_circ_223881,RMVar_hsa_circ_223879,RMVar_hsa_circ_223880,RMVar_hsa_circ_299304,RMVar_hsa_circ_320763,RMVar_hsa_circ_223882,RMVar_hsa_circ_223884,RMVar_hsa_circ_223883,RMVar_hsa_circ_311286,RMVar_hsa_circ_378331 89382 RMVar_ID_89382 Human_SNP_ID_169442359 m1A Human chr3 - 196075346 196075346 196075346 CCTTTTTCCGCAACACAGTTTGGTGGAGAACCATTGTCATATACCCGGTTCAGCCTGGCTCGGCA CCTTTTTCCGCAACACAGTTTGGTGGAGAACCGTTGTCATATACCCGGTTCAGCCTGGCTCGGCA T C TFRC Ensembl:ENSG00000072274 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:196075295..196075393 26863196 MeRIP-seq:(Medium) rs746921045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66642,Human_RBP_ID_938254,Human_RBP_ID_1624559,Human_RBP_ID_3964555,Human_RBP_ID_4756923,Human_RBP_ID_5530770,Human_RBP_ID_18002459,Human_RBP_ID_22092912,Human_RBP_ID_22456455,Human_RBP_ID_22678388,Human_RBP_ID_25724781 Human_Splice_Rec_529928,Human_Splice_Rec_529998,Human_Splice_Rec_530086,Human_Splice_Rec_530094 RMVar_hsa_circ_121595,RMVar_hsa_circ_223843,RMVar_hsa_circ_308948,RMVar_hsa_circ_4933,RMVar_hsa_circ_223854,RMVar_hsa_circ_341777,RMVar_hsa_circ_59092,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223865,RMVar_hsa_circ_223866,RMVar_hsa_circ_223867,RMVar_hsa_circ_329308,RMVar_hsa_circ_35376,RMVar_hsa_circ_297912,RMVar_hsa_circ_115479,RMVar_hsa_circ_223875,RMVar_hsa_circ_70073,RMVar_hsa_circ_325076,RMVar_hsa_circ_48394,RMVar_hsa_circ_223878,RMVar_hsa_circ_98087,RMVar_hsa_circ_279359,RMVar_hsa_circ_315825,RMVar_hsa_circ_223877,RMVar_hsa_circ_287545,RMVar_hsa_circ_223881,RMVar_hsa_circ_223879,RMVar_hsa_circ_223880,RMVar_hsa_circ_299304,RMVar_hsa_circ_320763,RMVar_hsa_circ_223882,RMVar_hsa_circ_223884,RMVar_hsa_circ_223883,RMVar_hsa_circ_311286,RMVar_hsa_circ_378331 89383 RMVar_ID_89383 Human_SNP_ID_169444161 m1A Human chr3 + 196081773 196081773 196081773 GGCAAGAAGGCAGAGAGAAGGGAAGGGACGAGAGGCGAAGGGACGAGAGGCGCAGGGACGCCTCT GGCAAGAAGGCAGAGAGAAGGGAAGGGACGAGGGGCGAAGGGACGAGAGGCGCAGGGACGCCTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196081771..196082100 26863196 MeRIP-seq:(Medium) rs937284301 Functional Loss SNV dbSNP153 33..33 33 - - - 89384 RMVar_ID_89384 Human_SNP_ID_169444164 m1A Human chr3 + 196081778 196081778 196081778 GAAGGCAGAGAGAAGGGAAGGGACGAGAGGCGAAGGGACGAGAGGCGCAGGGACGCCTCTGCGCA GAAGGCAGAGAGAAGGGAAGGGACGAGAGGCGCAGGGACGAGAGGCGCAGGGACGCCTCTGCGCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196081774..196082100 26863196 MeRIP-seq:(Medium) rs192657752 Functional Loss SNV dbSNP153 33..33 33 - - - 89385 RMVar_ID_89385 Human_SNP_ID_169444231 m1A Human chr3 + 196081979 196081979 196081979 TGGCTGCTGGACAGCACCGGAGCGGCCGCTCCAGCCAGCCCCGCAGGATGAAGGGAGGACACGAG TGGCTGCTGGACAGCACCGGAGCGGCCGCTCCTGCCAGCCCCGCAGGATGAAGGGAGGACACGAG A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:196081970..196082057 26863410 MeRIP-seq:(Medium) rs1300750553 Functional Loss SNV dbSNP153 33..33 33 - - - 89386 RMVar_ID_89386 Human_SNP_ID_169491361 m1A Human chr3 - 196247448 196247448 196247448 ACGGTGATGAACGAGAATGAGCGCTATGACGCAGTCCAGCACTGCCGCTACGTGGATGAGGTGGT ACGGTGATGAACGAGAATGAGCGCTATGACGCTGTCCAGCACTGCCGCTACGTGGATGAGGTGGT T A PCYT1A Ensembl:ENSG00000161217 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:196247426..196247450 32194978 MeRIP-seq:(Medium) rs368322216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933529,Human_RBP_ID_9394499,Human_RBP_ID_19011288,Human_RBP_ID_22092638 Human_Splice_Rec_530284,Human_Splice_Rec_530285,Human_Splice_Rec_530292,Human_Splice_Rec_530293,Human_Splice_Rec_530312,Human_Splice_Rec_530313,Human_Splice_Rec_530328,Human_Splice_Rec_530329,Human_Splice_Rec_530346,Human_Splice_Rec_530347,Human_Splice_Rec_530353,Human_Splice_Rec_530362,Human_Splice_Rec_530363,Human_Splice_Rec_530373,Human_Splice_Rec_530378,Human_Splice_Rec_530379,Human_Splice_Rec_530387,Human_Splice_Rec_530397,Human_Splice_Rec_530406,Human_Splice_Rec_530416,Human_Splice_Rec_530432 Human_miRNA_ID_1980195,Human_miRNA_ID_1981921,Human_miRNA_ID_2456592,Human_miRNA_ID_2461503,Human_miRNA_ID_2541352,Human_miRNA_ID_2543239,Human_miRNA_ID_2545091,Human_miRNA_ID_2546939,Human_miRNA_ID_2548806,Human_miRNA_ID_2550671,Human_miRNA_ID_2556075,Human_miRNA_ID_2557956,Human_miRNA_ID_2588373,Human_miRNA_ID_2634161,Human_miRNA_ID_2636848,Human_miRNA_ID_2773691 RMVar_hsa_circ_79342,RMVar_hsa_circ_112875,RMVar_hsa_circ_223886,RMVar_hsa_circ_223887,RMVar_hsa_circ_223888,RMVar_hsa_circ_122899,RMVar_hsa_circ_46685,RMVar_hsa_circ_223889,RMVar_hsa_circ_300119,RMVar_hsa_circ_223892,RMVar_hsa_circ_223894,RMVar_hsa_circ_92469,RMVar_hsa_circ_328031,RMVar_hsa_circ_223893 89387 RMVar_ID_89387 Human_SNP_ID_169491362 m1A Human chr3 - 196247448 196247448 196247448 ACGGTGATGAACGAGAATGAGCGCTATGACGCAGTCCAGCACTGCCGCTACGTGGATGAGGTGGT ACGGTGATGAACGAGAATGAGCGCTATGACGCCGTCCAGCACTGCCGCTACGTGGATGAGGTGGT T G PCYT1A Ensembl:ENSG00000161217 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:196247426..196247450 32194978 MeRIP-seq:(Medium) rs368322216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933529,Human_RBP_ID_9394499,Human_RBP_ID_19011288,Human_RBP_ID_22092638 Human_Splice_Rec_530284,Human_Splice_Rec_530285,Human_Splice_Rec_530292,Human_Splice_Rec_530293,Human_Splice_Rec_530312,Human_Splice_Rec_530313,Human_Splice_Rec_530328,Human_Splice_Rec_530329,Human_Splice_Rec_530346,Human_Splice_Rec_530347,Human_Splice_Rec_530353,Human_Splice_Rec_530362,Human_Splice_Rec_530363,Human_Splice_Rec_530373,Human_Splice_Rec_530378,Human_Splice_Rec_530379,Human_Splice_Rec_530387,Human_Splice_Rec_530397,Human_Splice_Rec_530406,Human_Splice_Rec_530416,Human_Splice_Rec_530432 Human_miRNA_ID_1980195,Human_miRNA_ID_1981921,Human_miRNA_ID_2456592,Human_miRNA_ID_2461503,Human_miRNA_ID_2541352,Human_miRNA_ID_2543239,Human_miRNA_ID_2545091,Human_miRNA_ID_2546939,Human_miRNA_ID_2548806,Human_miRNA_ID_2550671,Human_miRNA_ID_2556075,Human_miRNA_ID_2557956,Human_miRNA_ID_2588373,Human_miRNA_ID_2634161,Human_miRNA_ID_2636848,Human_miRNA_ID_2773691 RMVar_hsa_circ_79342,RMVar_hsa_circ_112875,RMVar_hsa_circ_223886,RMVar_hsa_circ_223887,RMVar_hsa_circ_223888,RMVar_hsa_circ_122899,RMVar_hsa_circ_46685,RMVar_hsa_circ_223889,RMVar_hsa_circ_300119,RMVar_hsa_circ_223892,RMVar_hsa_circ_223894,RMVar_hsa_circ_92469,RMVar_hsa_circ_328031,RMVar_hsa_circ_223893 89388 RMVar_ID_89388 Human_SNP_ID_169500709 m1A Human chr3 + 196287620 196287620 196287620 AACAGAGACGCAAAGATAGGCACACACCTGCAACTCACGCTCCCCCGAGCCCGGTCCGGTCGGAT AACAGAGACGCAAAGATAGGCACACACCTGCAGCTCACGCTCCCCCGAGCCCGGTCCGGTCGGAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196270426..196306952 26863196 MeRIP-seq:(Medium) rs543431029 Functional Loss SNV dbSNP153 33..33 33 - - - 89389 RMVar_ID_89389 Human_SNP_ID_169508588 m1A Human chr3 - 196317953 196317953 196317953 CGGAGCTCGCCTGGGACCTGGGCCACGGAAGGAGCGCGGGGGACGCGCGGGGTCCGCGGGGCGGG CGGAGCTCGCCTGGGACCTGGGCCACGGAAGGGGCGCGGGGGACGCGCGGGGTCCGCGGGGCGGG T C TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:196317918..196318015 26863196 MeRIP-seq:(Medium) rs1351402665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212244,Human_RBP_ID_1069257,Human_RBP_ID_3721080,Human_RBP_ID_26790355 89390 RMVar_ID_89390 Human_SNP_ID_169508669 m1A Human chr3 - 196318097 196318095 196318098 CTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGGAGCCCGAGAACACCTATA CTTCTCGGTGGGCGACGGGGTGCCTGAGGCT___AAGAACGCAGGGGAGCCCGAGAACACCTATA TCTC T TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196317591..196318300 26863196 MeRIP-seq:(Medium) rs1297750586 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 89391 RMVar_ID_89391 Human_SNP_ID_169508671 m1A Human chr3 - 196318097 196318097 196318097 CTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGGAGCCCGAGAACACCTATA CTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGGGAAGAACGCAGGGGAGCCCGAGAACACCTATA T C TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196317591..196318300 26863196 MeRIP-seq:(Medium) rs141412719 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 89392 RMVar_ID_89392 Human_SNP_ID_169508672 m1A Human chr3 - 196318097 196318097 196318097 CTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGGAGCCCGAGAACACCTATA CTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGCGAAGAACGCAGGGGAGCCCGAGAACACCTATA T G TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196317591..196318300 26863196 MeRIP-seq:(Medium) rs141412719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 89393 RMVar_ID_89393 Human_SNP_ID_169508682 m1A Human chr3 - 196318115 196318107 196318115 CACGTCCATCGGAGTGTCCTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGG CACGTCCATCGGAGTGTCCTTCTCGGTGGGCG________CCTGAGGCTGAGAAGAACGCAGGGG GCACCCCGT G TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:196318076..196318285 26863196 MeRIP-seq:(Medium) rs1359119962 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 89394 RMVar_ID_89394 Human_SNP_ID_169508684 m1A Human chr3 + 196318109 196318109 196318109 CGGGCTCCCCTGCGTTCTTCTCAGCCTCAGGCACCCCGTCGCCCACCGAGAAGGACACTCCGATG CGGGCTCCCCTGCGTTCTTCTCAGCCTCAGGCTCCCCGTCGCCCACCGAGAAGGACACTCCGATG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:196318026..196318200 32194978 MeRIP-seq:(Medium) rs752037300 Functional Loss SNV dbSNP153 33..33 33 - - - 89395 RMVar_ID_89395 Human_SNP_ID_169508687 m1A Human chr3 - 196318115 196318115 196318115 CACGTCCATCGGAGTGTCCTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGG CACGTCCATCGGAGTGTCCTTCTCGGTGGGCGCCGGGGTGCCTGAGGCTGAGAAGAACGCAGGGG T G TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:196318076..196318285 26863196 MeRIP-seq:(Medium) rs1446527339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 89396 RMVar_ID_89396 Human_SNP_ID_169508743 m1A Human chr3 - 196318202 196318202 196318202 GAGACGCTTTCCCTGCTGCCGGCCGCGACCGCAACCCGCTAGGCCTTCATCGCGAGCTACGCCCG GAGACGCTTTCCCTGCTGCCGGCCGCGACCGCGACCCGCTAGGCCTTCATCGCGAGCTACGCCCG T C TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196317636..196318283 26863196 MeRIP-seq:(Medium) rs753928443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757657,Human_RBP_ID_18499943,Human_RBP_ID_22092110 89397 RMVar_ID_89397 Human_SNP_ID_169508744 m1A Human chr3 - 196318202 196318202 196318202 GAGACGCTTTCCCTGCTGCCGGCCGCGACCGCAACCCGCTAGGCCTTCATCGCGAGCTACGCCCG GAGACGCTTTCCCTGCTGCCGGCCGCGACCGCCACCCGCTAGGCCTTCATCGCGAGCTACGCCCG T G TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196317636..196318283 26863196 MeRIP-seq:(Medium) rs753928443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757657,Human_RBP_ID_18499943,Human_RBP_ID_22092110 89398 RMVar_ID_89398 Human_SNP_ID_169518513 m1A Human chr3 - 196353293 196353293 196353293 TCTTCAATCTCCCGAAGAATCGTACAAAATGTATACTTTCTTCCCATGTTAAGAAAACAGGTATA TCTTCAATCTCCCGAAGAATCGTACAAAATGTGTACTTTCTTCCCATGTTAAGAAAACAGGTATA T C UBXN7 Ensembl:ENSG00000163960 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11185525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1959025,Human_RBP_ID_7175956,Human_RBP_ID_8870906,Human_RBP_ID_22398325,Human_RBP_ID_27716788 GWAS_ID_11645,GWAS_ID_11646,GWAS_ID_11647,GWAS_ID_11648,GWAS_ID_11649,GWAS_ID_11650,GWAS_ID_11651,GWAS_ID_11652,GWAS_ID_11653 89399 RMVar_ID_89399 Human_SNP_ID_169521157 m1A Human chr3 - 196363937 196363937 196363937 TAGATAAACTTTTCTTGATTTTGTTCGTTTTGATTTTTTTTTTTTTTTGAGATGGAGTCTCGCTC TAGATAAACTTTTCTTGATTTTGTTCGTTTTGTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTC T A UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:196363850..196363937 26863410 MeRIP-seq:(Medium) rs1413654957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10213,RMVar_hsa_circ_27464,RMVar_hsa_circ_367128,RMVar_hsa_circ_333043,RMVar_hsa_circ_277841,RMVar_hsa_circ_293799,RMVar_hsa_circ_223902,RMVar_hsa_circ_223903,RMVar_hsa_circ_368072,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_26570,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_223905 89400 RMVar_ID_89400 Human_SNP_ID_169539631 m1A Human chr3 + 196432372 196432372 196432372 GAACTGTTGAATTAACCCCTTCAGCGCCGAGGACGCCGCGGAGCCCCCGTGGGCAGCCATCTTAC GAACTGTTGAATTAACCCCTTCAGCGCCGAGGGCGCCGCGGAGCCCCCGTGGGCAGCCATCTTAC A G UBXN7-AS1 Ensembl:ENSG00000225822 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196432235..196432406 26863196 MeRIP-seq:(Medium) rs770894670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5299543 89401 RMVar_ID_89401 Human_SNP_ID_169547827 m1A Human chr3 - 196461743 196461743 196461743 AGTCTATTGTGGGAGAGTTGAGTCTGTATTGTAGGGGAGTTGAGTCTGTATTGTAGGGCAATTGA AGTCTATTGTGGGAGAGTTGAGTCTGTATTGTGGGGGAGTTGAGTCTGTATTGTAGGGCAATTGA T C RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196461565..196461765 26863196 MeRIP-seq:(Medium) rs1322059691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23992949 89402 RMVar_ID_89402 Human_SNP_ID_169547829 m1A Human chr3 + 196461747 196461747 196461747 TTGCCCTACAATACAGACTCAACTCCCCTACAATACAGACTCAACTCTCCCACAATAGACTCAAC TTGCCCTACAATACAGACTCAACTCCCCTACAGTACAGACTCAACTCTCCCACAATAGACTCAAC A G lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196461569..196461767 26863196 MeRIP-seq:(Medium) rs1394160543 Functional Loss SNV dbSNP153 33..33 33 - - - 89403 RMVar_ID_89403 Human_SNP_ID_169547831 m1A Human chr3 + 196461749 196461748 196461750 GCCCTACAATACAGACTCAACTCCCCTACAATACAGACTCAACTCTCCCACAATAGACTCAACTC GCCCTACAATACAGACTCAACTCCCCTACAAT__AGACTCAACTCTCCCACAATAGACTCAACTC TAC T lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196461698..196461781 26863196 MeRIP-seq:(Medium) rs1332022549 Functional Loss DEL dbSNP153 33..34 33 - - - 89404 RMVar_ID_89404 Human_SNP_ID_169547978 m1A Human chr3 - 196462092 196462092 196462092 TTGAGTCTACTGTGGGATAGTTGAGTCTGTACAGTGGGATAGTTGAGTCTGTATTGGGAGAGTTG TTGAGTCTACTGTGGGATAGTTGAGTCTGTACTGTGGGATAGTTGAGTCTGTATTGGGAGAGTTG T A RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196462041..196462130 26863196 MeRIP-seq:(Medium) rs1406844479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23992950 89405 RMVar_ID_89405 Human_SNP_ID_169548115 m1A Human chr3 + 196462416 196462416 196462416 CAACTCTCCCACAATACAGACTCAATTCTCCCACAATACAGACTCAACTCCCCTGCAATACAGAC CAACTCTCCCACAATACAGACTCAATTCTCCCGCAATACAGACTCAACTCCCCTGCAATACAGAC A G lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196462369..196462584 26863196 MeRIP-seq:(Medium) rs542389359 Functional Loss SNV dbSNP153 33..33 33 - - - 89406 RMVar_ID_89406 Human_SNP_ID_169548117 m1A Human chr3 + 196462421 196462420 196462422 CTCCCACAATACAGACTCAATTCTCCCACAATACAGACTCAACTCCCCTGCAATACAGACTCACC CTCCCACAATACAGACTCAATTCTCCCACAAT__AGACTCAACTCCCCTGCAATACAGACTCACC TAC T lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196462374..196462584 26863196 MeRIP-seq:(Medium) rs1305346250 Functional Loss DEL dbSNP153 33..34 33 - - - 89407 RMVar_ID_89407 Human_SNP_ID_169548120 m1A Human chr3 + 196462430 196462430 196462430 TACAGACTCAATTCTCCCACAATACAGACTCAACTCCCCTGCAATACAGACTCACCTATCCCACA TACAGACTCAATTCTCCCACAATACAGACTCACCTCCCCTGCAATACAGACTCACCTATCCCACA A C lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196462381..196462581 26863196 MeRIP-seq:(Medium) rs1159840312 Functional Loss SNV dbSNP153 33..33 33 - - - 89408 RMVar_ID_89408 Human_SNP_ID_169550550 m1A Human chr3 + 196470382 196470314 196470383 TTCAATGATCCAAACTGTCAGTCACCCCACCCAGCCTCATCTGGACCAGTTTCTGACGACCCAAT __________________________________CCTCATCTGGACCAGTTTCTGACGACCCAAT TCCTCATCTGGACCAGTTTCTGACCACCCAATCAGTTTCAATGATCCAAACTGTCAGTCACCCCACCCAG T lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:196470314..196470699 26863196 MeRIP-seq:(Medium) rs1560264184 Functional Loss DEL dbSNP153 1..34 33 - - - 89409 RMVar_ID_89409 Human_SNP_ID_169550572 m1A Human chr3 + 196470382 196470382 196470382 TTCAATGATCCAAACTGTCAGTCACCCCACCCAGCCTCATCTGGACCAGTTTCTGACGACCCAAT TTCAATGATCCAAACTGTCAGTCACCCCACCCGGCCTCATCTGGACCAGTTTCTGACGACCCAAT A G lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:196470314..196470699 26863196 MeRIP-seq:(Medium) rs1232112453 Functional Loss SNV dbSNP153 33..33 33 - - - 89410 RMVar_ID_89410 Human_SNP_ID_169550605 m1A Human chr3 + 196470542 196470541 196470543 GACTGTCAGTCACCCCATCCAGCCTCAGCCTCATCCTCATCTGGACCCGTTTCTGACCAACCACC GACTGTCAGTCACCCCATCCAGCCTCAGCCTC__CCTCATCTGGACCCGTTTCTGACCAACCACC CAT C lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:196470226..196470854;chr3:196470226..196470870 26863196 MeRIP-seq:(Medium) rs1368550502 Functional Loss DEL dbSNP153 33..34 33 - - - 89411 RMVar_ID_89411 Human_SNP_ID_169550606 m1A Human chr3 + 196470542 196470542 196470542 GACTGTCAGTCACCCCATCCAGCCTCAGCCTCATCCTCATCTGGACCCGTTTCTGACCAACCACC GACTGTCAGTCACCCCATCCAGCCTCAGCCTCTTCCTCATCTGGACCCGTTTCTGACCAACCACC A T lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:196470226..196470854;chr3:196470226..196470870 26863196 MeRIP-seq:(Medium) rs1307324783 Functional Loss SNV dbSNP153 33..33 33 - - - 89412 RMVar_ID_89412 Human_SNP_ID_169555813 m1A Human chr3 - 196487499 196487499 196487499 TGAAGAATACATACAGAGGTTGTTGGCAGAGGAGGAAGAAGAGGAAAAAAGACAGGCAGAAAAAA TGAAGAATACATACAGAGGTTGTTGGCAGAGGGGGAAGAAGAGGAAAAAAGACAGGCAGAAAAAA T C RNF168 Ensembl:ENSG00000163961 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196487401..196487600 26863196 MeRIP-seq:(Medium) rs146256685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70210,Human_RBP_ID_7176300,Human_RBP_ID_9349081,Human_RBP_ID_9394506,Human_RBP_ID_18413421,Human_RBP_ID_23026436,Human_RBP_ID_23115871,Human_RBP_ID_24547362,Human_RBP_ID_26347630,Human_RBP_ID_27822866 Human_Splice_Rec_530588,Human_Splice_Rec_530596 RMVar_hsa_circ_264962,RMVar_hsa_circ_223929,RMVar_hsa_circ_223927,RMVar_hsa_circ_367451,RMVar_hsa_circ_329243,RMVar_hsa_circ_327469,RMVar_hsa_circ_365899,RMVar_hsa_circ_223930,RMVar_hsa_circ_293614 89413 RMVar_ID_89413 Human_SNP_ID_169560474 m1A Human chr3 - 196503116 196503116 196503116 CCTCGCTGTCCGAGTGCCAGTGCGGGATCTGCATGGAAATCCTCGTGGAGCCCGTCACCCTCCCG CCTCGCTGTCCGAGTGCCAGTGCGGGATCTGCGTGGAAATCCTCGTGGAGCCCGTCACCCTCCCG T C RNF168 Ensembl:ENSG00000163961 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:196503001..196503200 26863196 MeRIP-seq:(Medium) rs1396409194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1624660,Human_RBP_ID_4736694,Human_RBP_ID_8871032,Human_RBP_ID_9261229,Human_RBP_ID_17404838,Human_RBP_ID_22092119,Human_RBP_ID_23993029 89414 RMVar_ID_89414 Human_SNP_ID_169560650 m1A Human chr3 + 196503592 196503592 196503592 CAGCCGGGCCCCGGGACGCGGCTCCGGGAGGAAGCCCGGGCTCCGGCTGCAGCATAACTTCCGCT CAGCCGGGCCCCGGGACGCGGCTCCGGGAGGAGGCCCGGGCTCCGGCTGCAGCATAACTTCCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196503541..196503718 26863196 MeRIP-seq:(Medium) rs112692343 Functional Loss SNV dbSNP153 33..33 33 - - - 89415 RMVar_ID_89415 Human_SNP_ID_169560690 m1A Human chr3 - 196503669 196503669 196503669 GCGGAGCTCTGGGAAACTGCGCCAGGCGCCCGAAAGGTGAACACGGGAGTCGCGCGTCTCCCCCG GCGGAGCTCTGGGAAACTGCGCCAGGCGCCCGTAAGGTGAACACGGGAGTCGCGCGTCTCCCCCG T A RNF168 Ensembl:ENSG00000163961 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196503620..196503755 26863196 MeRIP-seq:(Medium) rs1286155142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757661,Human_RBP_ID_9334023,Human_RBP_ID_18424388,Human_RBP_ID_26347635,Human_RBP_ID_27822868 89416 RMVar_ID_89416 Human_SNP_ID_169576358 m1A Human chr3 - 196561342 196561342 196561342 GGCTTGGGGTGAAGATGGAACTCCATTAGGACACACGCGGTTCCAAGGGGCTGATGATGTTACCA GGCTTGGGGTGAAGATGGAACTCCATTAGGACGCACGCGGTTCCAAGGGGCTGATGATGTTACCA T C WDR53 Ensembl:ENSG00000185798 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196561292..196561439 26863196 MeRIP-seq:(Medium) rs957705352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8650 89417 RMVar_ID_89417 Human_SNP_ID_169576409 m1A Human chr3 + 196561463 196561463 196561463 GCAGAGGACAGGAGAAGAATGCCCACCCGTCCACTTGACTGCCATAATGGTCCCGGAGACTCTGT GCAGAGGACAGGAGAAGAATGCCCACCCGTCCGCTTGACTGCCATAATGGTCCCGGAGACTCTGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:196561412..196566997 32194978 MeRIP-seq:(Medium) rs1464434134 Functional Loss SNV dbSNP153 33..33 33 - - - 89418 RMVar_ID_89418 Human_SNP_ID_169578448 m1A Human chr3 + 196568845 196568845 196568845 GCGCGCGGCGGACGCCCCCGGGCAGGGGCGGGAGTGGTGGAGGCGCCGGCGGTTGGCACTGACAG GCGCGCGGCGGACGCCCCCGGGCAGGGGCGGGGGTGGTGGAGGCGCCGGCGGTTGGCACTGACAG A G FBXO45 Ensembl:ENSG00000174013 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:196568626..196569228 26863196 MeRIP-seq:(Medium) rs1246926713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334024,Human_RBP_ID_17150517 89419 RMVar_ID_89419 Human_SNP_ID_169578456 m1A Human chr3 - 196568865 196568865 196568865 GAGCGGCTCGCTCACCGCCCCTGTCAGTGCCAACCGCCGGCGCCTCCACCACTCCCGCCCCTGCC GAGCGGCTCGCTCACCGCCCCTGTCAGTGCCATCCGCCGGCGCCTCCACCACTCCCGCCCCTGCC T A RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196568651..196569233 26863196 MeRIP-seq:(Medium) rs1560314317 Functional Loss SNV dbSNP153 33..33 33 - - - 89420 RMVar_ID_89420 Human_SNP_ID_169578459 m1A Human chr3 + 196568870 196568870 196568870 GGGCGGGAGTGGTGGAGGCGCCGGCGGTTGGCACTGACAGGGGCGGTGAGCGAGCCGCTCCGGTC GGGCGGGAGTGGTGGAGGCGCCGGCGGTTGGCCCTGACAGGGGCGGTGAGCGAGCCGCTCCGGTC A C FBXO45 Ensembl:ENSG00000174013 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:196568675..196569058 26863196 MeRIP-seq:(Medium) rs1303410020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4736770,Human_RBP_ID_9334024,Human_RBP_ID_17150517,Human_RBP_ID_21897825,Human_RBP_ID_27500705 89421 RMVar_ID_89421 Human_SNP_ID_169578488 m1A Human chr3 + 196568966 196568966 196568966 CGGCGGGAAGCGGCGGCGGCAGCGGCGGCCCTAGGGCCGGCTGGTGAGGCGATGGCGGCGCCGGC CGGCGGGAAGCGGCGGCGGCAGCGGCGGCCCTGGGGCCGGCTGGTGAGGCGATGGCGGCGCCGGC A G FBXO45 Ensembl:ENSG00000174013 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:196568926..196569065 26863196 MeRIP-seq:(Medium) rs1055008949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8943537,Human_RBP_ID_17150518 89422 RMVar_ID_89422 Human_SNP_ID_169618979 m1A Human chr3 - 196712184 196712184 196712184 CGGGACCTGGAATCCCTGTACGCCGAGGTGGGAGCCGGTGGACCGGTCCCCCAGCCGGCCCCCAC CGGGACCTGGAATCCCTGTACGCCGAGGTGGGCGCCGGTGGACCGGTCCCCCAGCCGGCCCCCAC T G CEP19 Ensembl:ENSG00000174007 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196712135..196712209 26863196 MeRIP-seq:(Medium) rs1391505847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757667 RMVar_hsa_circ_87628,RMVar_hsa_circ_223932 89423 RMVar_ID_89423 Human_SNP_ID_169626319 m1A Human chr3 - 196739928 196739928 196739928 GAGGGGAGGGGAGGGAGCCTTCGGCAATGGCGACGGCCCGGGCCGGAGGGGAAGCGGAACAACCG GAGGGGAGGGGAGGGAGCCTTCGGCAATGGCGGCGGCCCGGGCCGGAGGGGAAGCGGAACAACCG T C RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196739878..196740110 26863196 MeRIP-seq:(Medium) rs187239531 Functional Loss SNV dbSNP153 33..33 33 - - - 89424 RMVar_ID_89424 Human_SNP_ID_169626413 m1A Human chr3 - 196740112 196740112 196740112 AGGTCCCCGCCCCAGCGAGGCGCCTCGGTCAGAGCTCCCGGCGGGCTGCGGAGCCGCCCCGGGCT AGGTCCCCGCCCCAGCGAGGCGCCTCGGTCAGCGCTCCCGGCGGGCTGCGGAGCCGCCCCGGGCT T G RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:196739876..196740175 26863196 MeRIP-seq:(Medium) rs1432217825 Functional Loss SNV dbSNP153 33..33 33 - - - 89425 RMVar_ID_89425 Human_SNP_ID_169626425 m1A Human chr3 - 196740159 196740159 196740159 TGCGTCCCGCGCCGGCCGGCCTGTGTGCACTTACCCCGGGCAAGGCAAGGTCCCCGCCCCAGCGA TGCGTCCCGCGCCGGCCGGCCTGTGTGCACTTCCCCCGGGCAAGGCAAGGTCCCCGCCCCAGCGA T G RF00017-3663 RNACentral:URS0000926E08 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196740108..196740229 26863196 MeRIP-seq:(Medium) rs1296066257 Functional Loss SNV dbSNP153 33..33 33 - - - 89426 RMVar_ID_89426 Human_SNP_ID_169680253 m1A Human chr3 + 196937068 196937067 196937069 TAGCCTCCTCTCCCAGCATCGTAGTCCTGCCGATACTCATCCCGAACCTTTAATGGAAAGAATCC TAGCCTCCTCTCCCAGCATCGTAGTCCTGCCG__ACTCATCCCGAACCTTTAATGGAAAGAATCC GAT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:196936984..196937100;chr3:196936901..196937100 26863196 MeRIP-seq:(Medium) rs775784369 Functional Loss DEL dbSNP153 33..34 33 - - - 89427 RMVar_ID_89427 Human_SNP_ID_169681874 m1A Human chr3 - 196942397 196942387 196942398 CCGGGTGAGGGAGGCCGGGCCGCGAGACGGGAAGGCCCTGGGCAAGAACGCTGAGAAACGGTTTG CCGGGTGAGGGAGGCCGGGCCGCGAGACGGG___________CAAGAACGCTGAGAAACGGTTTG GCCCAGGGCCTT G NCBP2 Ensembl:ENSG00000114503 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:196942393..196942487 32194978 MeRIP-seq:(Medium) rs1253342501 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_936269,Human_RBP_ID_4759006,Human_RBP_ID_22609339,Human_RBP_ID_27822874 Human_Splice_Rec_530865,Human_Splice_Rec_530893,Human_Splice_Rec_530905 89428 RMVar_ID_89428 Human_SNP_ID_169682088 m1A Human chr3 - 196942709 196942709 196942709 CGGCCAGCAGCCGCCGCAGCACCATCTTCTCCAAGCGCCCGGAACCCGACCTCGCCGCCCTCGTC CGGCCAGCAGCCGCCGCAGCACCATCTTCTCCGAGCGCCCGGAACCCGACCTCGCCGCCCTCGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196942651..196942879 26863196 MeRIP-seq:(Medium) rs1404766808 Functional Loss SNV dbSNP153 33..33 33 - - - 89429 RMVar_ID_89429 Human_SNP_ID_169699905 m1A Human chr3 + 197002760 197002760 197002760 TGGCGCGGCCACAGTGGGGGACGAGGCAGGGCACGCGGCGTTCCCCGGGCTCGGCCTCCCTCCCA TGGCGCGGCCACAGTGGGGGACGAGGCAGGGCCCGCGGCGTTCCCCGGGCTCGGCCTCCCTCCCA A C MELTF-AS1 Ensembl:ENSG00000228109 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197002713..197002815 26863196 MeRIP-seq:(Medium) rs1218037680 Functional Loss SNV dbSNP153 33..33 33 - - - 89430 RMVar_ID_89430 Human_SNP_ID_169699906 m1A Human chr3 + 197002760 197002760 197002760 TGGCGCGGCCACAGTGGGGGACGAGGCAGGGCACGCGGCGTTCCCCGGGCTCGGCCTCCCTCCCA TGGCGCGGCCACAGTGGGGGACGAGGCAGGGCGCGCGGCGTTCCCCGGGCTCGGCCTCCCTCCCA A G MELTF-AS1 Ensembl:ENSG00000228109 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197002713..197002815 26863196 MeRIP-seq:(Medium) rs1218037680 Functional Loss SNV dbSNP153 33..33 33 - - - 89431 RMVar_ID_89431 Human_SNP_ID_169700082 m1A Human chr3 - 197003203 197003203 197003203 CGCCCACGGGCGCCACCTGGCGCTGCTACCTGAGGCGCCGCCCCCGGGCCCGCGCGGCCCTTCCC CGCCCACGGGCGCCACCTGGCGCTGCTACCTGCGGCGCCGCCCCCGGGCCCGCGCGGCCCTTCCC T G MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197002936..197003890 26863196 MeRIP-seq:(Medium) rs889463234 Functional Loss SNV dbSNP153 33..33 33 - - - 89432 RMVar_ID_89432 Human_SNP_ID_169700133 m1A Human chr3 + 197003327 197003327 197003327 CCTTCTGGATTCCAGCGCGAAGCCGCCGCGGAAACTCCCCGGGCGGGCATCGGAGCTCTGGGGCG CCTTCTGGATTCCAGCGCGAAGCCGCCGCGGAGACTCCCCGGGCGGGCATCGGAGCTCTGGGGCG A G MELTF-AS1 Ensembl:ENSG00000228109 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197003278..197003459 26863196 MeRIP-seq:(Medium) rs1283572374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87192,RMVar_hsa_circ_223969 89433 RMVar_ID_89433 Human_SNP_ID_169700259 m1A Human chr3 - 197003603 197003603 197003603 ACATGCGTGTGCTGCCTTTCTGGAAAGAGCGCATCTGGAAGGGCAGCAGGGGAAAGGAGCACAAA ACATGCGTGTGCTGCCTTTCTGGAAAGAGCGCTTCTGGAAGGGCAGCAGGGGAAAGGAGCACAAA T A MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197003554..197003762 26863196 MeRIP-seq:(Medium) rs1224969598 Functional Loss SNV dbSNP153 33..33 33 - - - 89434 RMVar_ID_89434 Human_SNP_ID_169700287 m1A Human chr3 + 197003676 197003676 197003676 TGGCCCCAGATCCTCCCCGCGCCGCCGTTTTGAGCGTTCACACTCATTACCCAGGTCCGTCTGGG TGGCCCCAGATCCTCCCCGCGCCGCCGTTTTGGGCGTTCACACTCATTACCCAGGTCCGTCTGGG A G MELTF-AS1 Ensembl:ENSG00000228109 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:197003590..197003759 26863196 MeRIP-seq:(Medium) rs117708038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_530990,Human_Splice_Rec_530996,Human_Splice_Rec_530997 RMVar_hsa_circ_87192,RMVar_hsa_circ_223969 89435 RMVar_ID_89435 Human_SNP_ID_169700323 m1A Human chr3 - 197003782 197003782 197003782 TCCGGGGAGGCGGGTGGAGGCCCGTTCGCAGCAGTCCAGGTGGGGTGTCCCGGGAGGATTTTGGC TCCGGGGAGGCGGGTGGAGGCCCGTTCGCAGCGGTCCAGGTGGGGTGTCCCGGGAGGATTTTGGC T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197002985..197003812 26863196 MeRIP-seq:(Medium) rs982368148 Functional Loss SNV dbSNP153 33..33 33 - - - 89436 RMVar_ID_89436 Human_SNP_ID_169700488 m1A Human chr3 - 197004150 197004150 197004150 AGCAATTTGCAGCTAGCGGCACTGGGCGGGTGACCCTGCCTGAGCCCAGTGAGGAGCAGGTCGTC AGCAATTTGCAGCTAGCGGCACTGGGCGGGTGCCCCTGCCTGAGCCCAGTGAGGAGCAGGTCGTC T G MELTF Ensembl:ENSG00000163975 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197004009..197008882 32194978 MeRIP-seq:(Medium) rs1054072638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117909,RMVar_hsa_circ_223971,RMVar_hsa_circ_107726,RMVar_hsa_circ_223970 89437 RMVar_ID_89437 Human_SNP_ID_169701798 m1A Human chr3 - 197008964 197008964 197008964 CCCCTCATCATTGCCCTTCCCTCCACCCCAGCAGTGAGCGAGTTCTTCAATGCCAGCTGCGTGCC CCCCTCATCATTGCCCTTCCCTCCACCCCAGCGGTGAGCGAGTTCTTCAATGCCAGCTGCGTGCC T C MELTF Ensembl:ENSG00000163975 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197008926..197008975 32194978 MeRIP-seq:(Medium) rs1289084495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_530952 RMVar_hsa_circ_18293,RMVar_hsa_circ_117909,RMVar_hsa_circ_223971,RMVar_hsa_circ_107726,RMVar_hsa_circ_223970 89438 RMVar_ID_89438 Human_SNP_ID_169701960 m1A Human chr3 + 197009603 197009603 197009603 CCCAGAGAAGGCTTCCCCAGTCTGCGTTCCTAAAAAGGGGGGGGTACCTGTGAGGACGTCACAGT CCCAGAGAAGGCTTCCCCAGTCTGCGTTCCTACAAAGGGGGGGGTACCTGTGAGGACGTCACAGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197009601..197009775 32194978 MeRIP-seq:(Medium) rs201360557 Functional Loss SNV dbSNP153 33..33 33 - - - 89439 RMVar_ID_89439 Human_SNP_ID_169701961 m1A Human chr3 + 197009603 197009603 197009603 CCCAGAGAAGGCTTCCCCAGTCTGCGTTCCTAAAAAGGGGGGGGTACCTGTGAGGACGTCACAGT CCCAGAGAAGGCTTCCCCAGTCTGCGTTCCTATAAAGGGGGGGGTACCTGTGAGGACGTCACAGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197009601..197009775 32194978 MeRIP-seq:(Medium) rs201360557 Functional Loss SNV dbSNP153 33..33 33 - - - 89440 RMVar_ID_89440 Human_SNP_ID_169703419 m1A Human chr3 - 197015112 197015112 197015112 AGGGGACAGGCAGATAGGGGTGAGTCCCCTGGAGAGCCTGGGAGCTCCTCACTAAGTGGGGGTGC AGGGGACAGGCAGATAGGGGTGAGTCCCCTGGCGAGCCTGGGAGCTCCTCACTAAGTGGGGGTGC T G MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197015109..197015258 26863196 MeRIP-seq:(Medium) rs746189342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247647 RMVar_hsa_circ_18293,RMVar_hsa_circ_117909,RMVar_hsa_circ_223971,RMVar_hsa_circ_107726,RMVar_hsa_circ_223970 89441 RMVar_ID_89441 Human_SNP_ID_169703436 m1A Human chr3 - 197015175 197015175 197015175 GCACCCACCCCAGGGGACAGAGACAGGCGGGGAGGAGCGACCGCAGGGGCCAGCACCCACCCCAG GCACCCACCCCAGGGGACAGAGACAGGCGGGGGGGAGCGACCGCAGGGGCCAGCACCCACCCCAG T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197015170..197015325 26863196 MeRIP-seq:(Medium) rs1004812764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18293,RMVar_hsa_circ_117909,RMVar_hsa_circ_223971,RMVar_hsa_circ_107726,RMVar_hsa_circ_223970 89442 RMVar_ID_89442 Human_SNP_ID_169706816 m1A Human chr3 - 197025354 197025354 197025354 AGGATTGGTAAGAAACAAGGCGGGTGAGTCAGAGGATGGTACCAGACGGAGCTACTCAGGTTGGC AGGATTGGTAAGAAACAAGGCGGGTGAGTCAGGGGATGGTACCAGACGGAGCTACTCAGGTTGGC T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197025352..197025507 26863196 MeRIP-seq:(Medium) rs1036418538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18499951 RMVar_hsa_circ_18293 89443 RMVar_ID_89443 Human_SNP_ID_169707240 m1A Human chr3 + 197026748 197026748 197026748 TAGATGGCTCCTCCATCCAGAGTGATGGCGTCAGCCTCCTGGGCCTGCAAGGAAATGTGGCTCAG TAGATGGCTCCTCCATCCAGAGTGATGGCGTCGGCCTCCTGGGCCTGCAAGGAAATGTGGCTCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197026651..197026918 32194978 MeRIP-seq:(Medium) rs1478457811 Functional Loss SNV dbSNP153 33..33 33 - - - 89444 RMVar_ID_89444 Human_SNP_ID_169707597 m1A Human chr3 - 197027847 197027847 197027847 CACCTCGGACCCAGAGCAGCACAAGTGCGGCAACATGAGCGAGGCCTTCCGGGAAGCGGGCATCC CACCTCGGACCCAGAGCAGCACAAGTGCGGCACCATGAGCGAGGCCTTCCGGGAAGCGGGCATCC T G MELTF Ensembl:ENSG00000163975 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197027800..197027899 26863196 MeRIP-seq:(Medium) rs371422593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_530932,Human_Splice_Rec_530933,Human_Splice_Rec_530962,Human_Splice_Rec_530963,Human_Splice_Rec_530976,Human_Splice_Rec_530977,Human_Splice_Rec_530985 89445 RMVar_ID_89445 Human_SNP_ID_169708130 m1A Human chr3 - 197029491 197029491 197029491 CTCGGGGTCGAGTGAGGACGGCGGAGGGAACTAGCACTGAAGCGCAGACGGGGAAGTCTGGAAGG CTCGGGGTCGAGTGAGGACGGCGGAGGGAACTGGCACTGAAGCGCAGACGGGGAAGTCTGGAAGG T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197029479..197029590 26863196 MeRIP-seq:(Medium) rs1560228350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721112,Human_RBP_ID_5325417,Human_RBP_ID_5392417,Human_RBP_ID_8124732,Human_RBP_ID_8236247,Human_RBP_ID_9434783,Human_RBP_ID_18499957,Human_RBP_ID_22363323,Human_RBP_ID_22725895 89446 RMVar_ID_89446 Human_SNP_ID_169778696 m1A Human chr3 + 197297800 197297800 197297800 TCCGCGGGCCCCCACACCTGCGGCGCCGCCACAAAGTTCCGGTGAGCGGCGTGCGCTCGGAACTG TCCGCGGGCCCCCACACCTGCGGCGCCGCCACCAAGTTCCGGTGAGCGGCGTGCGCTCGGAACTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:197297769..197298080 26863196 MeRIP-seq:(Medium) rs1217362053 Functional Loss SNV dbSNP153 33..33 33 - - - 89447 RMVar_ID_89447 Human_SNP_ID_169778703 m1A Human chr3 - 197297819 197297819 197297819 GTCTGGCCGGGGCGCACCCCAGTTCCGAGCGCACGCCGCTCACCGGAACTTTGTGGCGGCGCCGC GTCTGGCCGGGGCGCACCCCAGTTCCGAGCGCCCGCCGCTCACCGGAACTTTGTGGCGGCGCCGC T G DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:197297769..197298056 26863196 MeRIP-seq:(Medium) rs1331688403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965944,Human_RBP_ID_9354461,Human_RBP_ID_22607370,Human_RBP_ID_26763495,Human_RBP_ID_26790259 RMVar_hsa_circ_120559,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_109228,RMVar_hsa_circ_224029 89448 RMVar_ID_89448 Human_SNP_ID_169778756 m1A Human chr3 + 197297923 197297923 197297923 CCGCCCCGCCCGGGGCCCGCGGAGCCGAGCGGAGGGGGCGAAGGGACGGGGGAGGAGCTCCCCTG CCGCCCCGCCCGGGGCCCGCGGAGCCGAGCGGCGGGGGCGAAGGGACGGGGGAGGAGCTCCCCTG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:197297651..197298100 26863196 MeRIP-seq:(Medium) rs1156277089 Functional Loss SNV dbSNP153 33..33 33 - - - 89449 RMVar_ID_89449 Human_SNP_ID_169778835 m1A Human chr3 + 197298050 197298050 197298050 GCCCCCCGGCCCGCTCGCCCAGTTGCTGCCGCACGCCCCACCCCCGGAACCTCGCCTCCTTCCGC GCCCCCCGGCCCGCTCGCCCAGTTGCTGCCGCTCGCCCCACCCCCGGAACCTCGCCTCCTTCCGC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr3:197297954..197298100;chr3:197298012..197298096 26863196,26863410 MeRIP-seq:(Medium) rs1368278881 Functional Loss SNV dbSNP153 33..33 33 - - - 89450 RMVar_ID_89450 Human_SNP_ID_169778840 m1A Human chr3 + 197298057 197298057 197298057 GGCCCGCTCGCCCAGTTGCTGCCGCACGCCCCACCCCCGGAACCTCGCCTCCTTCCGCGCCCCCA GGCCCGCTCGCCCAGTTGCTGCCGCACGCCCCCCCCCCGGAACCTCGCCTCCTTCCGCGCCCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197297575..197298439 26863196 MeRIP-seq:(Medium) rs551638202 Functional Loss SNV dbSNP153 33..33 33 - - - 89451 RMVar_ID_89451 Human_SNP_ID_169778841 m1A Human chr3 + 197298057 197298057 197298057 GGCCCGCTCGCCCAGTTGCTGCCGCACGCCCCACCCCCGGAACCTCGCCTCCTTCCGCGCCCCCA GGCCCGCTCGCCCAGTTGCTGCCGCACGCCCCGCCCCCGGAACCTCGCCTCCTTCCGCGCCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197297575..197298439 26863196 MeRIP-seq:(Medium) rs551638202 Functional Loss SNV dbSNP153 33..33 33 - - - 89452 RMVar_ID_89452 Human_SNP_ID_169778848 m1A Human chr3 + 197298065 197298065 197298065 CGCCCAGTTGCTGCCGCACGCCCCACCCCCGGAACCTCGCCTCCTTCCGCGCCCCCAACCGCTCT CGCCCAGTTGCTGCCGCACGCCCCACCCCCGGCACCTCGCCTCCTTCCGCGCCCCCAACCGCTCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:197297925..197298127 26863196 MeRIP-seq:(Medium) rs1264641893 Functional Loss SNV dbSNP153 33..33 33 - - - 89453 RMVar_ID_89453 Human_SNP_ID_169778850 m1A Human chr3 - 197298077 197298077 197298077 AAGTTTCGGGGGAGAGCGGTTGGGGGCGCGGAAGGAGGCGAGGTTCCGGGGGTGGGGCGTGCGGC AAGTTTCGGGGGAGAGCGGTTGGGGGCGCGGAGGGAGGCGAGGTTCCGGGGGTGGGGCGTGCGGC T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197297651..197298150 26863196 MeRIP-seq:(Medium) rs1016247628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_598437,Human_RBP_ID_933541,Human_RBP_ID_3964569,Human_RBP_ID_9334038,Human_RBP_ID_9354363,Human_RBP_ID_9434784,Human_RBP_ID_17671339,Human_RBP_ID_18424129,Human_RBP_ID_22725896,Human_RBP_ID_23026441 RMVar_hsa_circ_120559,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_109228,RMVar_hsa_circ_224029 89454 RMVar_ID_89454 Human_SNP_ID_169839036 m1A Human chr3 + 197517353 197517353 197517353 TGCTCTATGGTCTCCATCCCCCCCTCAGGCCGACCCCATCAGTCACTTCCTGCTGTATGTCTCCA TGCTCTATGGTCTCCATCCCCCCCTCAGGCCGCCCCCATCAGTCACTTCCTGCTGTATGTCTCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:197517350..197517523 26863196 MeRIP-seq:(Medium) rs1280734966 Functional Loss SNV dbSNP153 33..33 33 - - - 89455 RMVar_ID_89455 Human_SNP_ID_169839254 m1A Human chr3 - 197518085 197518085 197518085 GAAGTGACTGATTGGGGGGGGTCAGCCTGATGAGGAGATGGAGACCATAGAGCAGGAAGTGACTG GAAGTGACTGATTGGGGGGGGTCAGCCTGATGGGGAGATGGAGACCATAGAGCAGGAAGTGACTG T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:197518048..197518146 26863196 MeRIP-seq:(Medium) rs1393368466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721706,Human_RBP_ID_8209586 89456 RMVar_ID_89456 Human_SNP_ID_169839257 m1A Human chr3 - 197518094 197518094 197518094 ATAGAGCAGGAAGTGACTGATTGGGGGGGGTCAGCCTGATGAGGAGATGGAGACCATAGAGCAGG ATAGAGCAGGAAGTGACTGATTGGGGGGGGTCGGCCTGATGAGGAGATGGAGACCATAGAGCAGG T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197518041..197518187 26863196 MeRIP-seq:(Medium) rs1393185202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721706,Human_RBP_ID_8209586 89457 RMVar_ID_89457 Human_SNP_ID_169839389 m1A Human chr3 + 197518421 197518421 197518421 TGCTCTATGGACTCCATCCCCCCCTCAGGCCGACCTCCCCGATCAGTCACTTCCTGCTCTATGGT TGCTCTATGGACTCCATCCCCCCCTCAGGCCGCCCTCCCCGATCAGTCACTTCCTGCTCTATGGT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197518260..197518572 26863196 MeRIP-seq:(Medium) rs1175303449 Functional Loss SNV dbSNP153 33..33 33 - - - 89458 RMVar_ID_89458 Human_SNP_ID_169839595 m1A Human chr3 + 197518904 197518904 197518904 CTGCTCTATGGTCTCCATCCCCCCTCAGGCTGACCTCCCCGCCCCATCAGTCACTTCCTGCTCTA CTGCTCTATGGTCTCCATCCCCCCTCAGGCTGCCCTCCCCGCCCCATCAGTCACTTCCTGCTCTA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197518655..197519174 26863196 MeRIP-seq:(Medium) rs1379566795 Functional Loss SNV dbSNP153 33..33 33 - - - 89459 RMVar_ID_89459 Human_SNP_ID_169839596 m1A Human chr3 + 197518904 197518904 197518904 CTGCTCTATGGTCTCCATCCCCCCTCAGGCTGACCTCCCCGCCCCATCAGTCACTTCCTGCTCTA CTGCTCTATGGTCTCCATCCCCCCTCAGGCTGGCCTCCCCGCCCCATCAGTCACTTCCTGCTCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197518655..197519174 26863196 MeRIP-seq:(Medium) rs1379566795 Functional Loss SNV dbSNP153 33..33 33 - - - 89460 RMVar_ID_89460 Human_SNP_ID_169839863 m1A Human chr3 - 197519818 197519818 197519818 CCGGCCCCGACCCCCGCAGGACGCTGAGGGACAGGACATCTGGAGCCTGGGACCAGCCCTCCCTG CCGGCCCCGACCCCCGCAGGACGCTGAGGGACGGGACATCTGGAGCCTGGGACCAGCCCTCCCTG T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197519814..197519927 26863196 MeRIP-seq:(Medium) rs9868761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3721711,Human_RBP_ID_8210486 89461 RMVar_ID_89461 Human_SNP_ID_169840373 m1A Human chr3 + 197521728 197521728 197521728 GCGCCTCACCTCATCCCCACATCCAAGTCACCAAGTCCAGGCAGCTTCGCCTTCTCAACACTCCT GCGCCTCACCTCATCCCCACATCCAAGTCACCCAGTCCAGGCAGCTTCGCCTTCTCAACACTCCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:197521700..197522145 26863196 MeRIP-seq:(Medium) rs1369958405 Functional Loss SNV dbSNP153 33..33 33 - - - 89462 RMVar_ID_89462 Human_SNP_ID_169841313 m1A Human chr3 + 197525590 197525590 197525590 CACGGCTTCAGGCTCCCGAGGAGAGCAACGCTACCCTCCTATCTTCACTGACAGACCCACCCCAG CACGGCTTCAGGCTCCCGAGGAGAGCAACGCTGCCCTCCTATCTTCACTGACAGACCCACCCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197525588..197525726 26863196 MeRIP-seq:(Medium) rs1309584853 Functional Loss SNV dbSNP153 33..33 33 - - - 89463 RMVar_ID_89463 Human_SNP_ID_169841315 m1A Human chr3 + 197525598 197525598 197525598 CAGGCTCCCGAGGAGAGCAACGCTACCCTCCTATCTTCACTGACAGACCCACCCCAGGAACCCTC CAGGCTCCCGAGGAGAGCAACGCTACCCTCCTGTCTTCACTGACAGACCCACCCCAGGAACCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197525566..197525701 26863196 MeRIP-seq:(Medium) rs1560315042 Functional Loss SNV dbSNP153 33..33 33 - - - 89464 RMVar_ID_89464 Human_SNP_ID_169841797 m1A Human chr3 - 197527671 197527671 197527671 CCAGGAGGGAGTGTGCAGGGTGCATCTGAGAAACAGCATGAAGCCTCTGTGGCTGAAGCAGAATG CCAGGAGGGAGTGTGCAGGGTGCATCTGAGAACCAGCATGAAGCCTCTGTGGCTGAAGCAGAATG T G BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197527668..197527977 26863196 MeRIP-seq:(Medium) rs1215833386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769 89465 RMVar_ID_89465 Human_SNP_ID_169847614 m1A Human chr3 + 197552117 197552117 197552117 CCACTTGAATGTTTACTACGTATCTCAAATGCAACCTGTGCAAAACTGAGCCTGTGCTATTGTCC CCACTTGAATGTTTACTACGTATCTCAAATGCTACCTGTGCAAAACTGAGCCTGTGCTATTGTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197552113..197552211 26863196 MeRIP-seq:(Medium) rs191345671 Functional Loss SNV dbSNP153 33..33 33 - - - 89466 RMVar_ID_89466 Human_SNP_ID_169848587 m1A Human chr3 + 197555839 197555839 197555839 GCTGCAGAGGGCTCGCCGAGGCTCTCGCCTTCACCCGGCGCCGCGCAGGTGCCCGCTCTCCTGCG GCTGCAGAGGGCTCGCCGAGGCTCTCGCCTTCGCCCGGCGCCGCGCAGGTGCCCGCTCTCCTGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:197555795..197555983 26863196 MeRIP-seq:(Medium) rs6769884 Functional Loss SNV dbSNP153 33..33 33 - - - 89467 RMVar_ID_89467 Human_SNP_ID_169861957 m1A Human chr3 - 197603820 197603820 197603820 GGTGCAGCAAGCGTGGTGGAGAGAAAGACAGGAAAAGGCCAAGGGCAGTGTGGTCAGGCCCAGCT GGTGCAGCAAGCGTGGTGGAGAGAAAGACAGGGAAAGGCCAAGGGCAGTGTGGTCAGGCCCAGCT T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197603727..197603821 26863196 MeRIP-seq:(Medium) rs990708686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224035 89468 RMVar_ID_89468 Human_SNP_ID_169864408 m1A Human chr3 - 197612762 197612762 197612762 TGGTGGTACATGCCTGTAGTCCCAGCTACTCAAGAGGATGGGGCCAGAGGATCGCTTGAGCCTAG TGGTGGTACATGCCTGTAGTCCCAGCTACTCAGGAGGATGGGGCCAGAGGATCGCTTGAGCCTAG T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1409708452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3723308,Human_RBP_ID_5089816,Human_RBP_ID_5250080,Human_RBP_ID_8210957,Human_RBP_ID_8875817,Human_RBP_ID_14768157,Human_RBP_ID_17573973,Human_RBP_ID_18536356,Human_RBP_ID_21988314,Human_RBP_ID_22371973 89469 RMVar_ID_89469 Human_SNP_ID_169868589 m1A Human chr3 + 197627829 197627829 197627829 GCGCCAGGCGCCGAGCGCTTAGCAGCCGCGACAGGCTCCGGACCCCCGATACGTCTGCAGTCGCC GCGCCAGGCGCCGAGCGCTTAGCAGCCGCGACGGGCTCCGGACCCCCGATACGTCTGCAGTCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:197627695..197627843;chr3:197627694..197627851;chr3:197627708..197627834;chr3:197627676..197627900 26863196 MeRIP-seq:(Medium) rs1487286882 Functional Loss SNV dbSNP153 33..33 33 - - - 89470 RMVar_ID_89470 Human_SNP_ID_169871770 m1A Human chr3 - 197637703 197637703 197637703 CAGCTGGAGATCTGGTGGGGAGCTGATGTTCCAGTATGAGGGCCGTGCAGCTGGAGACCTGGTGG CAGCTGGAGATCTGGTGGGGAGCTGATGTTCCTGTATGAGGGCCGTGCAGCTGGAGACCTGGTGG T A lnc-RUBCN-2-001,lnc-RUBCN-2-001:2 RNACentral:URS0000D5BC4C,RNACentral:URS00008C0E9B lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197637614..197637729 26863196 MeRIP-seq:(Medium) rs1339875218 Functional Loss SNV dbSNP153 33..33 33 - - - 89471 RMVar_ID_89471 Human_SNP_ID_169872669 m1A Human chr3 - 197640013 197640013 197640013 GCTGCAGACCTGAAGAGGAGCTGATGTTCGAGATTGAGGGTCGTGCAGCTGAATACTTGGAGAGG GCTGCAGACCTGAAGAGGAGCTGATGTTCGAGTTTGAGGGTCGTGCAGCTGAATACTTGGAGAGG T A lnc-RUBCN-2-001,lnc-RUBCN-2-001:2 RNACentral:URS00008BB7A3,RNACentral:URS00008C0E9B lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197639970..197640064 26863196 MeRIP-seq:(Medium) rs1328501888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23021895 89472 RMVar_ID_89472 Human_SNP_ID_169875426 m1A Human chr3 - 197645752 197645752 197645752 CACTGATGTCTTAGGTTGTGGAGCTGAAGACAACGAAGGAGCCAGTGTGGCTGTTCTGTGAGACT CACTGATGTCTTAGGTTGTGGAGCTGAAGACAGCGAAGGAGCCAGTGTGGCTGTTCTGTGAGACT T C lnc-RUBCN-2-001 RNACentral:URS00008C0E9B lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:197645669..197645784 26863196 MeRIP-seq:(Medium) rs1241739282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23993802 89473 RMVar_ID_89473 Human_SNP_ID_169883838 m1A Human chr3 - 197673355 197673353 197673356 GAAGCTGATGAGAGCTTGAGCTGGCGGTAAGAAGGAGTCTCCCAGGGAAGTGGGAGAGGCATTAA GAAGCTGATGAGAGCTTGAGCTGGCGGTAAG___GAGTCTCCCAGGGAAGTGGGAGAGGCATTAA CCTT C RUBCN Ensembl:ENSG00000145016 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197673307..197673401 26863196 MeRIP-seq:(Medium) rs1173066046 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18013095,Human_RBP_ID_23993816,Human_RBP_ID_26510751 89474 RMVar_ID_89474 Human_SNP_ID_169896894 m1A Human chr3 - 197720041 197720041 197720041 ATGGAGAGAGATCGGTCAACAGGGCCAAGGGGACAGACAGTTAGACAGAAGGAGTACATTCTGGT ATGGAGAGAGATCGGTCAACAGGGCCAAGGGGTCAGACAGTTAGACAGAAGGAGTACATTCTGGT T A RUBCN Ensembl:ENSG00000145016 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197720038..197720236 26863196 MeRIP-seq:(Medium) rs142677088 Functional Loss SNV dbSNP153 33..33 33 - - - 89475 RMVar_ID_89475 Human_SNP_ID_169901522 m1A Human chr3 - 197736694 197736694 197736694 GCCCCGGATGCGGCCGGAGGGCGCGGGAATGGAGCTCGGAGGCGGCGAGGAGCGCCTGCCTGAGG GCCCCGGATGCGGCCGGAGGGCGCGGGAATGGCGCTCGGAGGCGGCGAGGAGCGCCTGCCTGAGG T G RUBCN Ensembl:ENSG00000145016 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197736483..197736863 26863196 MeRIP-seq:(Medium) rs1405278158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19011316,Human_RBP_ID_22509349 Human_Splice_Rec_533891,Human_Splice_Rec_534039,Human_Splice_Rec_534059 89476 RMVar_ID_89476 Human_SNP_ID_169901526 m1A Human chr3 - 197736709 197736709 197736709 AGAGGCGGCCTCACCGCCCCGGATGCGGCCGGAGGGCGCGGGAATGGAGCTCGGAGGCGGCGAGG AGAGGCGGCCTCACCGCCCCGGATGCGGCCGGCGGGCGCGGGAATGGAGCTCGGAGGCGGCGAGG T G RUBCN Ensembl:ENSG00000145016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197736601..197736882 26863196 MeRIP-seq:(Medium) rs749381708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19011316 Human_Splice_Rec_533891,Human_Splice_Rec_534039,Human_Splice_Rec_534059 89477 RMVar_ID_89477 Human_SNP_ID_169905085 m1A Human chr3 - 197749950 197749950 197749950 AACCGGTTCATGGCTGGAGACGTCGCGCCGAGAGCGGGCGCGGACAAGGCCGGAGTCGCAGGCCT AACCGGTTCATGGCTGGAGACGTCGCGCCGAGTGCGGGCGCGGACAAGGCCGGAGTCGCAGGCCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:197749901..197749950 32194978 MeRIP-seq:(Medium) rs1161280869 Functional Loss SNV dbSNP153 33..33 33 - - - 89478 RMVar_ID_89478 Human_SNP_ID_169905158 m1A Human chr3 + 197750086 197750086 197750086 ACAAAATAGATATGTCTTTGGGTGAGGGGCCGAGTTGGACCGAGTTGGAGTGCGGGGGAGGGCGC ACAAAATAGATATGTCTTTGGGTGAGGGGCCGCGTTGGACCGAGTTGGAGTGCGGGGGAGGGCGC A C FYTTD1 Ensembl:ENSG00000122068 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:197750068..197750419 26863196 MeRIP-seq:(Medium) rs541967493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17152401,Human_RBP_ID_19121072 89479 RMVar_ID_89479 Human_SNP_ID_169913619 m1A Human chr3 + 197778460 197778460 197778460 TCCCCTGCAGTTTGACATAAACAGTGTCGGAAAACAGGTAAAAAAACGTTTTCTGTATTTTCTTG TCCCCTGCAGTTTGACATAAACAGTGTCGGAAGACAGGTAAAAAAACGTTTTCTGTATTTTCTTG A G FYTTD1 Ensembl:ENSG00000122068 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:197778418..197781964 32194978 MeRIP-seq:(Medium) rs779438265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965954 Human_Splice_Rec_534107,Human_Splice_Rec_534137,Human_Splice_Rec_534169,Human_Splice_Rec_534171 RMVar_hsa_circ_100080,RMVar_hsa_circ_345105,RMVar_hsa_circ_224045,RMVar_hsa_circ_111863,RMVar_hsa_circ_298894,RMVar_hsa_circ_224052 89480 RMVar_ID_89480 Human_SNP_ID_169914592 m1A Human chr3 + 197782055 197782052 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTT___AAAAAAAAAACGTATAAAATAATGCCCTGAAA TTTA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs75658829 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_69843,Human_RBP_ID_598524 89481 RMVar_ID_89481 Human_SNP_ID_169914597 m1A Human chr3 + 197782055 197782054 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTTT_AAAAAAAAAACGTATAAAATAATGCCCTGAAA TA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1287058732 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_69843,Human_RBP_ID_598524 89482 RMVar_ID_89482 Human_SNP_ID_169914600 m1A Human chr3 + 197782055 197782055 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTTAAAAAAAAAACGTATAAAATAATGCCCTGAAA A T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs532153464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69843,Human_RBP_ID_598524 89483 RMVar_ID_89483 Human_SNP_ID_169914643 m1A Human chr3 + 197782227 197782227 197782227 GAAAGATAGAAATTGATTATTTTTATGATAGCAGTATTCAGGATCTCATCACCTTTGCCCGTGTT GAAAGATAGAAATTGATTATTTTTATGATAGCGGTATTCAGGATCTCATCACCTTTGCCCGTGTT A G FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1273557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2775707,Human_RBP_ID_8209982,Human_RBP_ID_14768615,Human_RBP_ID_22509350,Human_RBP_ID_24427672,Human_RBP_ID_24497395 Human_miRNA_ID_533128,Human_miRNA_ID_539336,Human_miRNA_ID_1255862 89484 RMVar_ID_89484 Human_SNP_ID_169916985 m1A Human chr3 - 197791356 197791356 197791356 CCTGCCCCGGAGCTTGGGCCGCAGTGAACACCAGGGAGGTTACCTCCCGACGCTACCGTGCCAGA CCTGCCCCGGAGCTTGGGCCGCAGTGAACACCGGGGAGGTTACCTCCCGACGCTACCGTGCCAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197791308..197791501 26863196 MeRIP-seq:(Medium) rs922276143 Functional Loss SNV dbSNP153 33..33 33 - - - 89485 RMVar_ID_89485 Human_SNP_ID_169942718 m1A Human chr3 + 197885349 197885349 197885349 CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs373565572 Functional Loss SNV dbSNP153 33..33 33 - - - 89486 RMVar_ID_89486 Human_SNP_ID_169942719 m1A Human chr3 + 197885349 197885349 197885349 CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGCTGAGGC A T LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs373565572 Functional Loss SNV dbSNP153 33..33 33 - - - 89487 RMVar_ID_89487 Human_SNP_ID_169957058 m1A Human chr3 - 197941197 197941196 197941198 GAAGGGAGGGAGGAAGGAAGGGAAAGAAAGAGACAGAGGAGAGAGGGGAGAGAGAGAGGAGAGAG GAAGGGAGGGAGGAAGGAAGGGAAAGAAAGA__CAGAGGAGAGAGGGGAGAGAGAGAGGAGAGAG GTC G IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197941044..197941208 26863196 MeRIP-seq:(Medium) rs1354288582 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_15878,RMVar_hsa_circ_73691,RMVar_hsa_circ_360087,RMVar_hsa_circ_36602 89488 RMVar_ID_89488 Human_SNP_ID_169957130 m1A Human chr3 - 197941325 197941325 197941325 GAAAGAAAGAGACAGAGGGGAGAGAGAGAGGAAGGAAGGAAGAAAGGGAAGGAGGGAGGAAAAGA GAAAGAAAGAGACAGAGGGGAGAGAGAGAGGACGGAAGGAAGAAAGGGAAGGAGGGAGGAAAAGA T G IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197941277..197941386 26863196 MeRIP-seq:(Medium) rs1388467635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15878,RMVar_hsa_circ_73691,RMVar_hsa_circ_360087,RMVar_hsa_circ_36602 89489 RMVar_ID_89489 Human_SNP_ID_169957157 m1A Human chr3 - 197941354 197941340 197941355 GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGAAAGAAAGAGACAGAGGGGAGAGAGAGAGGAAGGA GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGA_______________GGGAGAGAGAGAGGAAGGA CCTCTGTCTCTTTCTT C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197941307..197941377 26863196 MeRIP-seq:(Medium) rs1560111254 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_15878,RMVar_hsa_circ_73691,RMVar_hsa_circ_360087,RMVar_hsa_circ_36602 89490 RMVar_ID_89490 Human_SNP_ID_169957161 m1A Human chr3 - 197941354 197941341 197941355 GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGAAAGAAAGAGACAGAGGGGAGAGAGAGAGGAAGGA GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGA______________GGGGAGAGAGAGAGGAAGGA CTCTGTCTCTTTCTT C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197941307..197941377 26863196 MeRIP-seq:(Medium) rs1378378700 Functional Loss DEL dbSNP153 32..45 33 - - - RMVar_hsa_circ_15878,RMVar_hsa_circ_73691,RMVar_hsa_circ_360087,RMVar_hsa_circ_36602 89491 RMVar_ID_89491 Human_SNP_ID_169957174 m1A Human chr3 - 197941354 197941354 197941354 GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGAAAGAAAGAGACAGAGGGGAGAGAGAGAGGAAGGA GAGGGGAGAGAGGGAGGAAGGAAGGAAGGGAAGGAAAGAGACAGAGGGGAGAGAGAGAGGAAGGA T C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197941307..197941377 26863196 MeRIP-seq:(Medium) rs1382209088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15878,RMVar_hsa_circ_73691,RMVar_hsa_circ_360087,RMVar_hsa_circ_36602 89492 RMVar_ID_89492 Human_SNP_ID_169959649 m1A Human chr3 + 197950220 197950220 197950220 TCCTTCTCTTACCGCCATCTTGGCTCCTGTGGAGGTGAGTGAAGGGTCTGCTGCTGAAATTTGGG TCCTTCTCTTACCGCCATCTTGGCTCCTGTGGGGGTGAGTGAAGGGTCTGCTGCTGAAATTTGGG A G RPL35A Ensembl:ENSG00000182899 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:197950201..197950225 32194978 MeRIP-seq:(Medium) rs1304993212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246913,Human_RBP_ID_784190,Human_RBP_ID_835452,Human_RBP_ID_936687,Human_RBP_ID_1625033,Human_RBP_ID_4756948,Human_RBP_ID_5120473,Human_RBP_ID_17660734,Human_RBP_ID_18424446,Human_RBP_ID_18805620,Human_RBP_ID_19116565,Human_RBP_ID_22092926,Human_RBP_ID_22279435,Human_RBP_ID_22456459 Human_Splice_Rec_534621,Human_Splice_Rec_534627,Human_Splice_Rec_534635,Human_Splice_Rec_534643,Human_Splice_Rec_534651,Human_Splice_Rec_534653,Human_Splice_Rec_534657,Human_Splice_Rec_534665 RMVar_hsa_circ_113145,RMVar_hsa_circ_224129 89493 RMVar_ID_89493 Human_SNP_ID_169959651 m1A Human chr3 - 197950223 197950223 197950223 GCCCCCAAATTTCAGCAGCAGACCCTTCACTCACCTCCACAGGAGCCAAGATGGCGGTAAGAGAA GCCCCCAAATTTCAGCAGCAGACCCTTCACTCGCCTCCACAGGAGCCAAGATGGCGGTAAGAGAA T C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:197950201..197950591;chr3:197950201..197950353;chr3:197950201..197950343 26863196 MeRIP-seq:(Medium) rs908998236 Functional Loss SNV dbSNP153 33..33 33 - - - 89494 RMVar_ID_89494 Human_SNP_ID_169959667 m1A Human chr3 + 197950245 197950245 197950245 CCTGTGGAGGTGAGTGAAGGGTCTGCTGCTGAAATTTGGGGGCAAATAACCGGAGTAGGTTTGTT CCTGTGGAGGTGAGTGAAGGGTCTGCTGCTGATATTTGGGGGCAAATAACCGGAGTAGGTTTGTT A T RPL35A Ensembl:ENSG00000182899 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:197950243..197950368 26863196 MeRIP-seq:(Medium) rs577389743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936687,Human_RBP_ID_1385477,Human_RBP_ID_1625033,Human_RBP_ID_4737594,Human_RBP_ID_5447409,Human_RBP_ID_9138458,Human_RBP_ID_18424131,Human_RBP_ID_18805621,Human_RBP_ID_19116565,Human_RBP_ID_23258688,Human_RBP_ID_23994108 Human_Splice_Rec_534627 RMVar_hsa_circ_75562,RMVar_hsa_circ_113145,RMVar_hsa_circ_224129,RMVar_hsa_circ_91765,RMVar_hsa_circ_224130 89495 RMVar_ID_89495 Human_SNP_ID_169959872 m1A Human chr3 - 197950929 197950924 197950929 TTTTAGAAGTCCCGTTCCCAGCAGGCCTTAAAACAAACAAAAAGATTAGTTTAAAACCAAGCCAC TTTTAGAAGTCCCGTTCCCAGCAGGCCTTAAA_____CAAAAAGATTAGTTTAAAACCAAGCCAC GTTTGT G IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197950926..197950975 26863196 MeRIP-seq:(Medium) rs1560119750 Functional Loss DEL dbSNP153 33..37 33 - - - 89496 RMVar_ID_89496 Human_SNP_ID_169959874 m1A Human chr3 - 197950929 197950928 197950929 TTTTAGAAGTCCCGTTCCCAGCAGGCCTTAAAACAAACAAAAAGATTAGTTTAAAACCAAGCCAC TTTTAGAAGTCCCGTTCCCAGCAGGCCTTAAA_CAAACAAAAAGATTAGTTTAAAACCAAGCCAC GT G IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197950926..197950975 26863196 MeRIP-seq:(Medium) rs1366133909 Functional Loss DEL dbSNP153 33..33 33 - - - 89497 RMVar_ID_89497 Human_SNP_ID_169959953 m1A Human chr3 - 197951140 197951138 197951141 CCTTGGACCACAGCCTAAGACACAAAAGATACACAACATGAAACATAAGCTTCAAAAAACCAATC CCTTGGACCACAGCCTAAGACACAAAAGATA___AACATGAAACATAAGCTTCAAAAAACCAATC TGTG T IQCG Ensembl:ENSG00000114473 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197951137..197951268 26863196 MeRIP-seq:(Medium) rs1456590302 Functional Loss DEL dbSNP153 32..34 33 - - - 89498 RMVar_ID_89498 Human_SNP_ID_169960003 m1A Human chr3 + 197951264 197951263 197951265 AAAATTGAAGGTGTTTACGCCCGAGATGAAACAGAATTCTATTTGGGCAAGAGATGCGCTTATGT AAAATTGAAGGTGTTTACGCCCGAGATGAAAC__AATTCTATTTGGGCAAGAGATGCGCTTATGT CAG C RPL35A Ensembl:ENSG00000182899 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:197950926..197951344 32194978 MeRIP-seq:(Medium) rs1560120302 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_598653,Human_RBP_ID_784193,Human_RBP_ID_1204939,Human_RBP_ID_1385478,Human_RBP_ID_1625040,Human_RBP_ID_1959760,Human_RBP_ID_4737603,Human_RBP_ID_8569394,Human_RBP_ID_9138461,Human_RBP_ID_14770123,Human_RBP_ID_17661313,Human_RBP_ID_18013679,Human_RBP_ID_18805626,Human_RBP_ID_21897832,Human_RBP_ID_22457199,Human_RBP_ID_22509358,Human_RBP_ID_23994129,Human_RBP_ID_27316813 Human_Splice_Rec_534625,Human_Splice_Rec_534631,Human_Splice_Rec_534639,Human_Splice_Rec_534647,Human_Splice_Rec_534661,Human_Splice_Rec_534669,Human_Splice_Rec_534677,Human_Splice_Rec_534681 Human_miRNA_ID_2349459 Clinvar_Rec_505 RMVar_hsa_circ_59217,RMVar_hsa_circ_75562,RMVar_hsa_circ_113145,RMVar_hsa_circ_224129,RMVar_hsa_circ_224130,RMVar_hsa_circ_124389,RMVar_hsa_circ_88697,RMVar_hsa_circ_224132,RMVar_hsa_circ_224133 89499 RMVar_ID_89499 Human_SNP_ID_169962753 m1A Human chr3 - 197960275 197960275 197960275 CACCGGCTCCGGCCCGGGCCTGAGCCCGAGTAACCCACTCCTCCGCCCCATTCGGCCGCCATCTT CACCGGCTCCGGCCCGGGCCTGAGCCCGAGTAGCCCACTCCTCCGCCCCATTCGGCCGCCATCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197960252..197960367 26863196 MeRIP-seq:(Medium) rs745653923 Functional Loss SNV dbSNP153 33..33 33 - - - 89500 RMVar_ID_89500 Human_SNP_ID_169962754 m1A Human chr3 - 197960275 197960275 197960275 CACCGGCTCCGGCCCGGGCCTGAGCCCGAGTAACCCACTCCTCCGCCCCATTCGGCCGCCATCTT CACCGGCTCCGGCCCGGGCCTGAGCCCGAGTACCCCACTCCTCCGCCCCATTCGGCCGCCATCTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:197960252..197960367 26863196 MeRIP-seq:(Medium) rs745653923 Functional Loss SNV dbSNP153 33..33 33 - - - 89501 RMVar_ID_89501 Human_SNP_ID_169962794 m1A Human chr3 + 197960315 197960315 197960315 GCTCAGGCCCGGGCCGGAGCCGGTGGCGCTGGAGCGGGTCTGTGTGGGTCCGAAGCGTTTTACTC GCTCAGGCCCGGGCCGGAGCCGGTGGCGCTGGGGCGGGTCTGTGTGGGTCCGAAGCGTTTTACTC A G LMLN Ensembl:ENSG00000185621 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197960268..197960424 26863196 MeRIP-seq:(Medium) rs779866874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_534689,Human_Splice_Rec_534823 89502 RMVar_ID_89502 Human_SNP_ID_169962802 m1A Human chr3 + 197960336 197960336 197960336 GGTGGCGCTGGAGCGGGTCTGTGTGGGTCCGAAGCGTTTTACTCCTGTTGGGCGGGCTCCGGGCC GGTGGCGCTGGAGCGGGTCTGTGTGGGTCCGATGCGTTTTACTCCTGTTGGGCGGGCTCCGGGCC A T LMLN Ensembl:ENSG00000185621 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:197960265..197960382;chr3:197960287..197960410 26863196 MeRIP-seq:(Medium) rs766515162 Functional Loss SNV dbSNP153 33..33 33 - - - 89503 RMVar_ID_89503 Human_SNP_ID_169981601 m1A Human chr3 + 198038977 198038977 198038977 TCAGCAACCCAGCCACCTTCATCAGCAACCCAACCACCTCATCAGCAACCCAGCCACCTTCATCA TCAGCAACCCAGCCACCTTCATCAGCAACCCAGCCACCTCATCAGCAACCCAGCCACCTTCATCA A G LMLN Ensembl:ENSG00000185621 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:198038830..198039050 26863196 MeRIP-seq:(Medium) rs562573910 Functional Loss SNV dbSNP153 33..33 33 - - - 89504 RMVar_ID_89504 Human_SNP_ID_311747285 m1A Human chr7 - 16646210 16646210 16646210 ATTCGTGCAGCAGCAGCGGCAGCAGCAGCAGCAGCAGCAGTGGCGGCAGACAATGGAGGAGTGAA ATTCGTGCAGCAGCAGCGGCAGCAGCAGCAGCGGCAGCAGTGGCGGCAGACAATGGAGGAGTGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:16646151..16646337;chr7:16646151..16646354 26863196 MeRIP-seq:(Medium) rs114469613 Functional Loss SNV dbSNP153 33..33 33 - - - 89505 RMVar_ID_89505 Human_SNP_ID_311747288 m1A Human chr7 - 16646213 16646213 16646213 GCGATTCGTGCAGCAGCAGCGGCAGCAGCAGCAGCAGCAGCAGTGGCGGCAGACAATGGAGGAGT GCGATTCGTGCAGCAGCAGCGGCAGCAGCAGCGGCAGCAGCAGTGGCGGCAGACAATGGAGGAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:16646151..16646336;chr7:16646151..16646342 26863196 MeRIP-seq:(Medium) rs1054854200 Functional Loss SNV dbSNP153 33..33 33 - - - 89506 RMVar_ID_89506 Human_SNP_ID_311747314 m1A Human chr7 - 16646270 16646270 16646270 GGGCTGCTTCTCACCTGTCCGAGGAGGTAGCGACGACGCGCAAGGCTGGGGGCTGCGGCGATTCG GGGCTGCTTCTCACCTGTCCGAGGAGGTAGCGTCGACGCGCAAGGCTGGGGGCTGCGGCGATTCG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:16646179..16646279 32194978 MeRIP-seq:(Medium) rs998760546 Functional Loss SNV dbSNP153 33..33 33 - - - 89507 RMVar_ID_89507 Human_SNP_ID_311752475 m1A Human chr7 - 16665428 16665420 16665429 TTCTGATGCTTATTCATAAAATTTCTGAAAACAAAGAAAATAAAGATTATGTATTTCAGATAAGC TTCTGATGCTTATTCATAAAATTTCTGAAAA_________TAAAGATTATGTATTTCAGATAAGC ATTTTCTTTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:16665426..16665525;chr7:16665426..16665500 26863196 MeRIP-seq:(Medium) rs1484818738 Functional Loss DEL dbSNP153 32..40 33 - - - 89508 RMVar_ID_89508 Human_SNP_ID_311928435 m1A Human chr7 - 17298972 17298972 17298972 CAAGGCGGCGCAGGTGCCGTCTACACCGGCGGAGGCGGCGCGGCAATGCCCGCAGGTGAGGCGGC CAAGGCGGCGCAGGTGCCGTCTACACCGGCGGCGGCGGCGCGGCAATGCCCGCAGGTGAGGCGGC T G AC073332.1 Ensembl:ENSG00000237773 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:17298922..17299069 26863196 MeRIP-seq:(Medium) rs1406803402 Functional Loss SNV dbSNP153 33..33 33 - - - 89509 RMVar_ID_89509 Human_SNP_ID_311940202 m1A Human chr7 + 17345208 17345208 17345208 ATGGTGGCGTGAGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCCTGAACCTG ATGGTGGCGTGAGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATAGCCTGAACCTG A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1283192947 Functional Loss SNV dbSNP153 33..33 33 - - - 89510 RMVar_ID_89510 Human_SNP_ID_312116128 m1A Human chr7 + 17942014 17942014 17942014 AGGATACCAAGAGATACTAGAGACAACAAGGAACCTGGAAAAAGATAGTGTTCCAACCTGTAAAT AGGATACCAAGAGATACTAGAGACAACAAGGAGCCTGGAAAAAGATAGTGTTCCAACCTGTAAAT A G AC080080.1 Ensembl:ENSG00000279048 Other exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:17942011..17942093 26863410 MeRIP-seq:(Medium) rs1282310558 Functional Loss SNV dbSNP153 33..33 33 - - - 89511 RMVar_ID_89511 Human_SNP_ID_312396780 m1A Human chr7 - 18980716 18980682 18980716 AAGGAAGAAGAAGAAGAAGAAGGAAGAAGAAGAGGAAGAAGGAAGAAGAAGGAAGAAGAACAAGA AAGGAAGAAGAAGAAGAAGAAGGAAGAAGAAG_________________________________ CTTCTTGTTCTTCTTCCTTCTTCTTCCTTCTTCCT C lnc-TWIST1-4 RNACentral:URS00008BCB77 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:18980669..18980775 26863196 MeRIP-seq:(Medium) rs779897058 Functional Loss DEL dbSNP153 33..65 33 - - - 89512 RMVar_ID_89512 Human_SNP_ID_312396818 m1A Human chr7 - 18980716 18980714 18980716 AAGGAAGAAGAAGAAGAAGAAGGAAGAAGAAGAGGAAGAAGGAAGAAGAAGGAAGAAGAACAAGA AAGGAAGAAGAAGAAGAAGAAGGAAGAAGAAG__GAAGAAGGAAGAAGAAGGAAGAAGAACAAGA CCT C lnc-TWIST1-4 RNACentral:URS00008BCB77 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:18980669..18980775 26863196 MeRIP-seq:(Medium) rs1491137559 Functional Loss DEL dbSNP153 33..34 33 - - - 89513 RMVar_ID_89513 Human_SNP_ID_312438788 m1A Human chr7 - 19117468 19117468 19117468 CTCCCCGCCTCCCCCGCGCGCCCTCCCCGCGGAGGTCCCTCCCGTCCGTCCTCCTGCTCTCTCCT CTCCCCGCCTCCCCCGCGCGCCCTCCCCGCGGTGGTCCCTCCCGTCCGTCCTCCTGCTCTCTCCT T A TWIST1 Ensembl:ENSG00000122691 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:19117275..19117573 26863410 MeRIP-seq:(Medium) rs1002706240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5452167 89514 RMVar_ID_89514 Human_SNP_ID_312809020 m1A Human chr7 - 20345512 20345512 20345512 GGCTCAAACACTGGTCTTTTTTCATGAGGCTTACCCCATCTAATCTACTTGAAATGGCAACTCTG GGCTCAAACACTGGTCTTTTTTCATGAGGCTTGCCCCATCTAATCTACTTGAAATGGCAACTCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:20345465..20345605 26863196 MeRIP-seq:(Medium) rs1311584971 Functional Loss SNV dbSNP153 33..33 33 - - - 89515 RMVar_ID_89515 Human_SNP_ID_313109303 m1A Human chr7 - 21428101 21428097 21428102 AGCTGGCACAGGCTCTGCCTCTTTTTCCGCGAATGGCCGCCGCTGGGCTGTGGCGTAGCAGCTCC AGCTGGCACAGGCTCTGCCTCTTTTTCCGCG_____CCGCCGCTGGGCTGTGGCGTAGCAGCTCC GCCATT G lnc-CDCA7L-2 RNACentral:URS00008B7581 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:21428003..21428179 26863196 MeRIP-seq:(Medium) rs1189695653 Functional Loss DEL dbSNP153 32..36 33 - - - 89516 RMVar_ID_89516 Human_SNP_ID_313257533 m1A Human chr7 - 21901281 21901224 21901281 AACATGCTAGAAAATCCTCACTGCACTCCAGCAGAGGCTAGAGGAATGCCAGTGTTACCTTACGC AACATGCTAGAAAATCCTCACTGCACTCCAGC_________________________________ GGCTGGAGTGGCTCTGCTTCTAGAAGCGTAAGGTAACACTGGCATTCCTCTAGCCTCT G CDCA7L Ensembl:ENSG00000164649 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:21901147..21901595 32194978 MeRIP-seq:(Medium) rs1554294478 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_680873,Human_RBP_ID_18380836,Human_RBP_ID_24206682 Clinvar_Rec_506 89517 RMVar_ID_89517 Human_SNP_ID_313257577 m1A Human chr7 - 21901281 21901281 21901281 AACATGCTAGAAAATCCTCACTGCACTCCAGCAGAGGCTAGAGGAATGCCAGTGTTACCTTACGC AACATGCTAGAAAATCCTCACTGCACTCCAGCCGAGGCTAGAGGAATGCCAGTGTTACCTTACGC T G CDCA7L Ensembl:ENSG00000164649 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:21901147..21901595 32194978 MeRIP-seq:(Medium) rs1562615070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_680873,Human_RBP_ID_18380836,Human_RBP_ID_24206682 89518 RMVar_ID_89518 Human_SNP_ID_313271547 m1A Human chr7 + 21945850 21945850 21945850 GCTCCAGTCTCCTCCCAGCACGCGGCCACGGGAGCCCGGACTCACCACGGCCCGGCGCACCAAGA GCTCCAGTCTCCTCCCAGCACGCGGCCACGGGGGCCCGGACTCACCACGGCCCGGCGCACCAAGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:21945692..21945850 26863196 MeRIP-seq:(Medium) rs1041456797 Functional Loss SNV dbSNP153 33..33 33 - - - 89519 RMVar_ID_89519 Human_SNP_ID_313465023 m1A Human chr7 - 22727272 22727270 22727273 GGCTAAGGATTTCCTGCACTTACTTGTGGAGAAGGAGTTCATAGCTGGGCTCCTGGAGGGGAGAT GGCTAAGGATTTCCTGCACTTACTTGTGGAG___GAGTTCATAGCTGGGCTCCTGGAGGGGAGAT CCTT C STEAP1B,IL6-AS1 Ensembl:ENSG00000105889,Ensembl:ENSG00000179428 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:22727221..22727312 26863196 MeRIP-seq:(Medium) rs1034241131 Functional Loss DEL dbSNP153 32..34 33 - - - 89520 RMVar_ID_89520 Human_SNP_ID_313465025 m1A Human chr7 - 22727272 22727272 22727272 GGCTAAGGATTTCCTGCACTTACTTGTGGAGAAGGAGTTCATAGCTGGGCTCCTGGAGGGGAGAT GGCTAAGGATTTCCTGCACTTACTTGTGGAGACGGAGTTCATAGCTGGGCTCCTGGAGGGGAGAT T G STEAP1B,IL6-AS1 Ensembl:ENSG00000105889,Ensembl:ENSG00000179428 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:22727221..22727312 26863196 MeRIP-seq:(Medium) rs958965295 Functional Loss SNV dbSNP153 33..33 33 - - - 89521 RMVar_ID_89521 Human_SNP_ID_313465149 m1A Human chr7 + 22727520 22727520 22727520 TTGCCTGCTGCCTTCCCTGCCCCAGTACCCCCAGGAGAAGATTCCAAAGATGTAGCCGCCCCACA TTGCCTGCTGCCTTCCCTGCCCCAGTACCCCCGGGAGAAGATTCCAAAGATGTAGCCGCCCCACA A G IL6 Ensembl:ENSG00000136244 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:22727423..22727547 26863196 MeRIP-seq:(Medium) rs758406611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_848930,Human_Splice_Rec_848938,Human_Splice_Rec_848954,Human_Splice_Rec_848968,Human_Splice_Rec_848976 RMVar_hsa_circ_27527 89522 RMVar_ID_89522 Human_SNP_ID_313488270 m1A Human chr7 - 22813125 22813125 22813125 TCTTCTGGATTTGGAGGCAATCAGCGGACAGCATGGAAGATGTGTGCTCTGGCTCGGATAAGAGA TCTTCTGGATTTGGAGGCAATCAGCGGACAGCTTGGAAGATGTGTGCTCTGGCTCGGATAAGAGA T A TOMM7 Ensembl:ENSG00000196683 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:22813076..22813150 32194978 MeRIP-seq:(Medium) rs1310903811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254548,Human_RBP_ID_680954,Human_RBP_ID_794708,Human_RBP_ID_1051469,Human_RBP_ID_1220794,Human_RBP_ID_1684905,Human_RBP_ID_2039641,Human_RBP_ID_3840869,Human_RBP_ID_4935307,Human_RBP_ID_5152917,Human_RBP_ID_7723354,Human_RBP_ID_8664395,Human_RBP_ID_9209119,Human_RBP_ID_9337731,Human_RBP_ID_16111173,Human_RBP_ID_17664256,Human_RBP_ID_17712784,Human_RBP_ID_18107949,Human_RBP_ID_18880281,Human_RBP_ID_22464395,Human_RBP_ID_23139948,Human_RBP_ID_23215428,Human_RBP_ID_24206928,Human_RBP_ID_27110597,Human_RBP_ID_27355703 Human_Splice_Rec_848984,Human_Splice_Rec_848988,Human_Splice_Rec_848990,Human_Splice_Rec_848994,Human_Splice_Rec_849000 Human_miRNA_ID_1748202 RMVar_hsa_circ_266094 89523 RMVar_ID_89523 Human_SNP_ID_313488286 m1A Human chr7 + 22813179 22813179 22813179 AATCCAGAAGACCAAATAATCCTTTATCCCCAAAGTAGGCTAAAATGTTTGTGAAGAGAAGAAAG AATCCAGAAGACCAAATAATCCTTTATCCCCAGAGTAGGCTAAAATGTTTGTGAAGAGAAGAAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:22813082..22813237 26863196 MeRIP-seq:(Medium) rs1445667931 Functional Loss SNV dbSNP153 33..33 33 - - - 89524 RMVar_ID_89524 Human_SNP_ID_313489521 m1A Human chr7 + 22817948 22817948 22817948 GCCACTATTACTCTTTTACATCTTAGTGATTCAGTACTACTGTATGAACATTTGTCCTGAAATGT GCCACTATTACTCTTTTACATCTTAGTGATTCCGTACTACTGTATGAACATTTGTCCTGAAATGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:22817945..22818094 26863196 MeRIP-seq:(Medium) rs1479305393 Functional Loss SNV dbSNP153 33..33 33 - - - 89525 RMVar_ID_89525 Human_SNP_ID_313490914 m1A Human chr7 - 22822725 22822725 22822725 CCAAGCAGAGACTACAGCAGCTCTTCAAGGGGAGCCAGTTTGCCATTCGCTGGGGCTTTATCCCT CCAAGCAGAGACTACAGCAGCTCTTCAAGGGGGGCCAGTTTGCCATTCGCTGGGGCTTTATCCCT T C TOMM7 Ensembl:ENSG00000196683 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:22822627..22822825 26863196 MeRIP-seq:(Medium) rs879066674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_680965,Human_RBP_ID_1684910,Human_RBP_ID_2039646,Human_RBP_ID_3840878,Human_RBP_ID_4956216,Human_RBP_ID_5122712,Human_RBP_ID_5328405,Human_RBP_ID_8664404,Human_RBP_ID_17664975,Human_RBP_ID_22463908,Human_RBP_ID_23215754,Human_RBP_ID_24206959,Human_RBP_ID_24515849 Human_Splice_Rec_848983,Human_Splice_Rec_848985,Human_Splice_Rec_848995,Human_Splice_Rec_849001,Human_Splice_Rec_849003 89526 RMVar_ID_89526 Human_SNP_ID_313490930 m1A Human chr7 - 22822754 22822754 22822754 CGTCGCCATGGTGAAGCTGAGCAAAGAGGCCAAGCAGAGACTACAGCAGCTCTTCAAGGGGAGCC CGTCGCCATGGTGAAGCTGAGCAAAGAGGCCAGGCAGAGACTACAGCAGCTCTTCAAGGGGAGCC T C TOMM7 Ensembl:ENSG00000196683 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:22822703..22822850 26863196 MeRIP-seq:(Medium) rs754168840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3840878,Human_RBP_ID_4935309,Human_RBP_ID_5328405,Human_RBP_ID_23215754,Human_RBP_ID_26831190,Human_RBP_ID_27110602 Human_Splice_Rec_848983,Human_Splice_Rec_848985,Human_Splice_Rec_848995,Human_Splice_Rec_849001,Human_Splice_Rec_849003 89527 RMVar_ID_89527 Human_SNP_ID_313499083 m1A Human chr7 - 22854282 22854282 22854282 GGCTCCTGCGTCCAGAAGGTCCGAGCCCACTTACCCAGTCACGCGCCGCGGCCGAAAAGGGAGGG GGCTCCTGCGTCCAGAAGGTCCGAGCCCACTTGCCCAGTCACGCGCCGCGGCCGAAAAGGGAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:22854274..22854343 26863196 MeRIP-seq:(Medium) rs1458396870 Functional Loss SNV dbSNP153 33..33 33 - - - 89528 RMVar_ID_89528 Human_SNP_ID_313533376 m1A Human chr7 - 22991135 22991135 22991135 GTTAACATTTTTCTATGTTAATTTTCAGGTTGAAGGTTTAGAACAGATGTGGAAAAATGTTTACT GTTAACATTTTTCTATGTTAATTTTCAGGTTGGAGGTTTAGAACAGATGTGGAAAAATGTTTACT T C FAM126A Ensembl:ENSG00000122591 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:22991123..22991208 26863196 MeRIP-seq:(Medium) rs779339655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24207153 Human_Splice_Rec_849106,Human_Splice_Rec_849107,Human_Splice_Rec_849146,Human_Splice_Rec_849147,Human_Splice_Rec_849174,Human_Splice_Rec_849175,Human_Splice_Rec_849182,Human_Splice_Rec_849183,Human_Splice_Rec_849188,Human_Splice_Rec_849189,Human_Splice_Rec_849192,Human_Splice_Rec_849193 RMVar_hsa_circ_21197,RMVar_hsa_circ_294628,RMVar_hsa_circ_244065,RMVar_hsa_circ_126458,RMVar_hsa_circ_244066,RMVar_hsa_circ_315755,RMVar_hsa_circ_287799,RMVar_hsa_circ_244067,RMVar_hsa_circ_365644,RMVar_hsa_circ_21100,RMVar_hsa_circ_244074,RMVar_hsa_circ_244073,RMVar_hsa_circ_279848,RMVar_hsa_circ_123419,RMVar_hsa_circ_244075 89529 RMVar_ID_89529 Human_SNP_ID_313538839 m1A Human chr7 - 23014034 23014033 23014034 ATGGCTCACCGGGACCCGTTCTGCTAGGAAGAAGGGGAGCAGGTGGTGCTGCTACTCGGGAGGAA ATGGCTCACCGGGACCCGTTCTGCTAGGAAGA_GGGGAGCAGGTGGTGCTGCTACTCGGGAGGAA CT C FAM126A Ensembl:ENSG00000122591 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:23013926..23014125 26863196 MeRIP-seq:(Medium) rs1255730874 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_176838,Human_RBP_ID_4956221,Human_RBP_ID_9404315,Human_RBP_ID_18425973,Human_RBP_ID_19020615,Human_RBP_ID_22111657 89530 RMVar_ID_89530 Human_SNP_ID_313585538 m1A Human chr7 - 23191186 23191186 23191186 CAATTAGGCCCAACATGATCTGGCCCCTGGCTATCTCTCTGGCCTTACTGTCATATTACTTTCCC CAATTAGGCCCAACATGATCTGGCCCCTGGCTCTCTCTCTGGCCTTACTGTCATATTACTTTCCC T G lnc-IGF2BP3-1 RNACentral:URS00008B217B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:23191040..23191404;chr7:23191073..23191306 26863196 MeRIP-seq:(Medium) rs1303355858 Functional Loss SNV dbSNP153 33..33 33 - - - 89531 RMVar_ID_89531 Human_SNP_ID_313588111 m1A Human chr7 + 23200272 23200272 23200272 CTGCCTCTTCTGGAAGCCCTGCTGGTTTTGGGAGTTCCCCAGCATTTGGAGCTGCAGCCTCTACC CTGCCTCTTCTGGAAGCCCTGCTGGTTTTGGGTGTTCCCCAGCATTTGGAGCTGCAGCCTCTACC A T NUP42 Ensembl:ENSG00000136243 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs752409597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_315602,Human_RBP_ID_681201,Human_RBP_ID_22111660 Human_miRNA_ID_51932,Human_miRNA_ID_343693,Human_miRNA_ID_1360668 RMVar_hsa_circ_244095,RMVar_hsa_circ_244094 89532 RMVar_ID_89532 Human_SNP_ID_313600187 m1A Human chr7 - 23246842 23246842 23246842 TAGTAGAGACATTCCATGCTGAATTCTCACGGACGCAGGCACTCAAGGTTTAACTCTGAATTCCT TAGTAGAGACATTCCATGCTGAATTCTCACGGTCGCAGGCACTCAAGGTTTAACTCTGAATTCCT T A lnc-IGF2BP3-1 RNACentral:URS00008B217B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:23246791..23246872 26863196 MeRIP-seq:(Medium) rs761042616 Functional Loss SNV dbSNP153 33..33 33 - - - 89533 RMVar_ID_89533 Human_SNP_ID_313614090 m1A Human chr7 - 23299384 23299384 23299384 AGGAAACCGCCCTGCGCCACATTAGTGGGGCGAGCAGCCGCGCCACACGGCCGCCCGGCCCCATA AGGAAACCGCCCTGCGCCACATTAGTGGGGCGGGCAGCCGCGCCACACGGCCGCCCGGCCCCATA T C lnc-IGF2BP3-1 RNACentral:URS00008B217B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23299326..23299498 26863196 MeRIP-seq:(Medium) rs1475622546 Functional Loss SNV dbSNP153 33..33 33 - - - 89534 RMVar_ID_89534 Human_SNP_ID_313614222 m1A Human chr7 + 23299578 23299578 23299578 CTGGGCTGGAGGAGCGGGCGGAGGGGACGGTCAACGAGGGACGCCCAGAATCGGACGCGGCAGGT CTGGGCTGGAGGAGCGGGCGGAGGGGACGGTCTACGAGGGACGCCCAGAATCGGACGCGGCAGGT A T MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:23299326..23300962 26863196 MeRIP-seq:(Medium) rs1469961115 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_953103,Human_RBP_ID_8944153,Human_RBP_ID_9337071,Human_RBP_ID_22110683,Human_RBP_ID_22463910,Human_RBP_ID_23120572 Human_Splice_Rec_849539,Human_Splice_Rec_849543,Human_Splice_Rec_849549 89535 RMVar_ID_89535 Human_SNP_ID_313615142 m1A Human chr7 + 23302401 23302401 23302401 GTCATAGAGGAGGCAGTTAAGACCAAAAGAGTAGCCAAAATTGTATAGAGAAAGGTTGTAAAATA GTCATAGAGGAGGCAGTTAAGACCAAAAGAGTGGCCAAAATTGTATAGAGAAAGGTTGTAAAATA A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:23302396..23302565 26863196 MeRIP-seq:(Medium) rs1311425559 Functional Loss SNV dbSNP153 33..33 33 - - - 89536 RMVar_ID_89536 Human_SNP_ID_313615156 m1A Human chr7 - 23302449 23302449 23302449 CTTCTGCTCTGTCATGTACCAGGGTTTTGTGTATAGGCCCCACCTTTTTATTTTACAACCTTTCT CTTCTGCTCTGTCATGTACCAGGGTTTTGTGTGTAGGCCCCACCTTTTTATTTTACAACCTTTCT T C lnc-IGF2BP3-1 RNACentral:URS00008B217B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23302444..23302574 26863196 MeRIP-seq:(Medium) rs1186896424 Functional Loss SNV dbSNP153 33..33 33 - - - 89537 RMVar_ID_89537 Human_SNP_ID_313617729 m1A Human chr7 + 23310856 23310852 23310856 GATCAGTGTAACATGACTGTGATCATCTTACAAACAAAACTCAAAAAATCAATTCAGAGAGCAGC GATCAGTGTAACATGACTGTGATCATCTT____ACAAAACTCAAAAAATCAATTCAGAGAGCAGC TACAA T MALSU1 Ensembl:ENSG00000156928 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:23310805..23310955 32194978 MeRIP-seq:(Medium) rs1385301651 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_8664564 89538 RMVar_ID_89538 Human_SNP_ID_313618333 m1A Human chr7 + 23312822 23312822 23312822 GGTGTCTGGTCACGAGGGACAACAACTTCTGCACTTGACAAATTCTGAAGTTCATTCACCTGAAA GGTGTCTGGTCACGAGGGACAACAACTTCTGCGCTTGACAAATTCTGAAGTTCATTCACCTGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:23312771..23313545 32194978 MeRIP-seq:(Medium) rs149038713 Functional Loss SNV dbSNP153 33..33 33 - - - 89539 RMVar_ID_89539 Human_SNP_ID_313648401 m1A Human chr7 - 23415043 23415043 23415043 ACAGATGGGGACCTGCGGGTGGGGTGATGCTGACTGACGGATGGGACCTGGTGATGCGGTGATAC ACAGATGGGGACCTGCGGGTGGGGTGATGCTGGCTGACGGATGGGACCTGGTGATGCGGTGATAC T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23414795..23415451 26863196 MeRIP-seq:(Medium) rs1267908232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844074,Human_RBP_ID_3080670,Human_RBP_ID_5242980,Human_RBP_ID_9439226,Human_RBP_ID_17543179,Human_RBP_ID_22554626,Human_RBP_ID_22622648,Human_RBP_ID_22728802,Human_RBP_ID_22746866,Human_RBP_ID_23120475,Human_RBP_ID_24207763,Human_RBP_ID_26794388,Human_RBP_ID_27574386 RMVar_hsa_circ_55845,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112,RMVar_hsa_circ_271728,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_309326,RMVar_hsa_circ_108481,RMVar_hsa_circ_14733,RMVar_hsa_circ_244125,RMVar_hsa_circ_280355,RMVar_hsa_circ_102538,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127 89540 RMVar_ID_89540 Human_SNP_ID_313648467 m1A Human chr7 + 23415224 23415224 23415224 ACTGCAACACCAGGTCCCGTCCGTCAGTCGGCATCAACGCATCACCAGGTCCCTACCCATCAGTC ACTGCAACACCAGGTCCCGTCCGTCAGTCGGCGTCAACGCATCACCAGGTCCCTACCCATCAGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:23415175..23415441 26863196 MeRIP-seq:(Medium) rs1374077020 Functional Loss SNV dbSNP153 33..33 33 - - - 89541 RMVar_ID_89541 Human_SNP_ID_313664418 m1A Human chr7 + 23470661 23470661 23470661 AGCCACGTGTTCAAACTACAAATCAACGTCTCACGTGAGGAATCCCAGAGCCTCAATTAGAGTGG AGCCACGTGTTCAAACTACAAATCAACGTCTCGCGTGAGGAATCCCAGAGCCTCAATTAGAGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:23470611..23470839 26863196 MeRIP-seq:(Medium) rs1378494357 Functional Loss SNV dbSNP153 33..33 33 - - - 89542 RMVar_ID_89542 Human_SNP_ID_313670173 m1A Human chr7 + 23490572 23490572 23490572 AGTGGCATCCGGGTCCGGGGTCACGGCCGTGGATGGGGCCGGGGCCGGGGTCGCGGCCGTGGATG AGTGGCATCCGGGTCCGGGGTCACGGCCGTGGGTGGGGCCGGGGCCGGGGTCGCGGCCGTGGATG A G RPS2P32 Ensembl:ENSG00000232818 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:23490521..23490692 26863196 MeRIP-seq:(Medium) rs1286742006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9440472 89543 RMVar_ID_89543 Human_SNP_ID_313675463 m1A Human chr7 + 23506194 23506194 23506194 TATCTGTCATACCCACGATCATATCCTCTATCATAGTAAGAATCTCGACGTCTGCCACCACCTCC TATCTGTCATACCCACGATCATATCCTCTATCGTAGTAAGAATCTCGACGTCTGCCACCACCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23505819..23506326 26863196 MeRIP-seq:(Medium) rs781242490 Functional Loss SNV dbSNP153 33..33 33 - - - 89544 RMVar_ID_89544 Human_SNP_ID_313675467 m1A Human chr7 + 23506202 23506202 23506202 ATACCCACGATCATATCCTCTATCATAGTAAGAATCTCGACGTCTGCCACCACCTCCACCTCCAC ATACCCACGATCATATCCTCTATCATAGTAAGGATCTCGACGTCTGCCACCACCTCCACCTCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:23506151..23506319 26863196 MeRIP-seq:(Medium) rs199922031 Functional Loss SNV dbSNP153 33..33 33 - - - 89545 RMVar_ID_89545 Human_SNP_ID_313675484 m1A Human chr7 + 23506221 23506221 23506221 CTATCATAGTAAGAATCTCGACGTCTGCCACCACCTCCACCTCCACCGCCGCCGCCTCCTCCACC CTATCATAGTAAGAATCTCGACGTCTGCCACCGCCTCCACCTCCACCGCCGCCGCCTCCTCCACC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:23506219..23506319 26863410 MeRIP-seq:(Medium) rs779459316 Functional Loss SNV dbSNP153 33..33 33 - - - 89546 RMVar_ID_89546 Human_SNP_ID_313682219 m1A Human chr7 + 23528360 23528360 23528360 CTCCCGAGTAGCTGGGACTACAGACGCGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAG CTCCCGAGTAGCTGGGACTACAGACGCGCGCCGCCACGCCCAGCTAATTTTTGTATTTTTAGTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:23528353..23528418 26863196 MeRIP-seq:(Medium) rs1313305350 Functional Loss SNV dbSNP153 33..33 33 - - - 89547 RMVar_ID_89547 Human_SNP_ID_313683273 m1A Human chr7 + 23531856 23531856 23531856 TGTCGACGAGGCGCTCCCCAGAACTAAATAAGAGACAAGTCTCGGCTCGAGGGCCGATGGCCTAA TGTCGACGAGGCGCTCCCCAGAACTAAATAAGGGACAAGTCTCGGCTCGAGGGCCGATGGCCTAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:23531826..23531975 26863196 MeRIP-seq:(Medium) rs377639677 Functional Loss SNV dbSNP153 33..33 33 - - - 89548 RMVar_ID_89548 Human_SNP_ID_313683308 m1A Human chr7 + 23531922 23531922 23531922 TAACCCGCTGACTGGACCGTGGGGAAGAGGAAAGAGTCGGCAACCACAGCCGCTCCACTCCACTC TAACCCGCTGACTGGACCGTGGGGAAGAGGAAGGAGTCGGCAACCACAGCCGCTCCACTCCACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:23531619..23531975 26863196 MeRIP-seq:(Medium) rs926552291 Functional Loss SNV dbSNP153 33..33 33 - - - 89549 RMVar_ID_89549 Human_SNP_ID_313683309 m1A Human chr7 + 23531924 23531924 23531924 ACCCGCTGACTGGACCGTGGGGAAGAGGAAAGAGTCGGCAACCACAGCCGCTCCACTCCACTCCC ACCCGCTGACTGGACCGTGGGGAAGAGGAAAGGGTCGGCAACCACAGCCGCTCCACTCCACTCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:23531845..23531975 26863196 MeRIP-seq:(Medium) rs1164391246 Functional Loss SNV dbSNP153 33..33 33 - - - 89550 RMVar_ID_89550 Human_SNP_ID_313683313 m1A Human chr7 + 23531937 23531932 23531938 ACCGTGGGGAAGAGGAAAGAGTCGGCAACCACAGCCGCTCCACTCCACTCCCACTCGGTCGCAGG ACCGTGGGGAAGAGGAAAGAGTCGGCAA______CCGCTCCACTCCACTCCCACTCGGTCGCAGG ACCACAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23531605..23531944 26863196 MeRIP-seq:(Medium) rs1261705231 Functional Loss DEL dbSNP153 29..34 33 - - - 89551 RMVar_ID_89551 Human_SNP_ID_313683317 m1A Human chr7 + 23531937 23531937 23531937 ACCGTGGGGAAGAGGAAAGAGTCGGCAACCACAGCCGCTCCACTCCACTCCCACTCGGTCGCAGG ACCGTGGGGAAGAGGAAAGAGTCGGCAACCACGGCCGCTCCACTCCACTCCCACTCGGTCGCAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23531605..23531944 26863196 MeRIP-seq:(Medium) rs1350427697 Functional Loss SNV dbSNP153 33..33 33 - - - 89552 RMVar_ID_89552 Human_SNP_ID_313712600 m1A Human chr7 + 23638224 23638224 23638224 GCCACGACCCCGTCTGGGAGGTGTGCCTAGCGACTCATTGGGGATGGGCCATGATGACAATGGCG GCCACGACCCCGTCTGGGAGGTGTGCCTAGCGGCTCATTGGGGATGGGCCATGATGACAATGGCG A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:23638173..23638257 26863196 MeRIP-seq:(Medium) rs372126479 Functional Loss SNV dbSNP153 33..33 33 - - - 89553 RMVar_ID_89553 Human_SNP_ID_313948342 m1A Human chr7 + 24573450 24573450 24573450 AGGAGAGAGAGGGAGGCGGAGGGCAGTGAGAGACGCATTTCCAGTTCTCAACTACGAGCCACGAG AGGAGAGAGAGGGAGGCGGAGGGCAGTGAGAGCCGCATTTCCAGTTCTCAACTACGAGCCACGAG A C MPP6 Ensembl:ENSG00000105926 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:24573277..24574185 26863196 MeRIP-seq:(Medium) rs1231981110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860498,Human_RBP_ID_8150470,Human_RBP_ID_8219550,Human_RBP_ID_8237696,Human_RBP_ID_9337081,Human_RBP_ID_9439227,Human_RBP_ID_18959143,Human_RBP_ID_22622660,Human_RBP_ID_26357630 89554 RMVar_ID_89554 Human_SNP_ID_313948352 m1A Human chr7 + 24573490 24573490 24573490 CCAGTTCTCAACTACGAGCCACGAGTTTGCAGATGGGGCTGCTCGGCGGCGCCTGTGGCTGAGGG CCAGTTCTCAACTACGAGCCACGAGTTTGCAGTTGGGGCTGCTCGGCGGCGCCTGTGGCTGAGGG A T MPP6 Ensembl:ENSG00000105926 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:24573439..24573711 26863196 MeRIP-seq:(Medium) rs1034874214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4962269,Human_RBP_ID_9439227,Human_RBP_ID_22110695,Human_RBP_ID_22321342,Human_RBP_ID_23215756 RMVar_hsa_circ_84425,RMVar_hsa_circ_89409,RMVar_hsa_circ_88166,RMVar_hsa_circ_244153,RMVar_hsa_circ_244154,RMVar_hsa_circ_244152 89555 RMVar_ID_89555 Human_SNP_ID_313948367 m1A Human chr7 + 24573541 24573541 24573541 CCTGTGGCTGAGGGAGAGCAGCGGCGGCGGGGAGCGACCGGGAGCGGCGGCAGCGGCGGCGCGGA CCTGTGGCTGAGGGAGAGCAGCGGCGGCGGGGGGCGACCGGGAGCGGCGGCAGCGGCGGCGCGGA A G MPP6 Ensembl:ENSG00000105926 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:24573321..24573600 26863196 MeRIP-seq:(Medium) rs973411995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22110695 Human_Splice_Rec_850221,Human_Splice_Rec_850229,Human_Splice_Rec_850251,Human_Splice_Rec_850271 RMVar_hsa_circ_84425,RMVar_hsa_circ_89409,RMVar_hsa_circ_88166,RMVar_hsa_circ_244153,RMVar_hsa_circ_244154,RMVar_hsa_circ_244152 89556 RMVar_ID_89556 Human_SNP_ID_313954544 m1A Human chr7 - 24595712 24595712 24595712 TCACTCTCCATCCTTTTAGTTTCATTTTCATCACAGTACTCATCTGAAATTATTTTTTGCTTATG TCACTCTCCATCCTTTTAGTTTCATTTTCATCGCAGTACTCATCTGAAATTATTTTTTGCTTATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:24595710..24596114 26863196 MeRIP-seq:(Medium) rs556861388 Functional Loss SNV dbSNP153 33..33 33 - - - 89557 RMVar_ID_89557 Human_SNP_ID_313954565 m1A Human chr7 + 24595783 24595783 24595783 TGTATGTAAGGGTGGTAGCGTAGTTTAGATTGAATGCTTGGGTTTACTTTCTGGGGAGGTAATAG TGTATGTAAGGGTGGTAGCGTAGTTTAGATTGCATGCTTGGGTTTACTTTCTGGGGAGGTAATAG A C MPP6 Ensembl:ENSG00000105926 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:24595781..24595969 26863196 MeRIP-seq:(Medium) rs1016237586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3081385,Human_RBP_ID_24208280 RMVar_hsa_circ_84425,RMVar_hsa_circ_89409,RMVar_hsa_circ_88166,RMVar_hsa_circ_244153,RMVar_hsa_circ_244154,RMVar_hsa_circ_244152 89558 RMVar_ID_89558 Human_SNP_ID_313961559 m1A Human chr7 - 24623614 24623614 24623614 ATAAAAACAAACAAACAAACAAACAAACAAAAACCCTTAAATTTCAAGCCGTTATGGAGTAAGAT ATAAAAACAAACAAACAAACAAACAAACAAAACCCCTTAAATTTCAAGCCGTTATGGAGTAAGAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:24623611..24623688;chr7:24623611..24623724 26863196 MeRIP-seq:(Medium) rs1047255555 Functional Loss SNV dbSNP153 33..33 33 - - - 89559 RMVar_ID_89559 Human_SNP_ID_313966787 m1A Human chr7 - 24641651 24641651 24641651 ACTTATTTGTTATTTGCACCAGACCATGGTTTATTTCTTTTTCGTAAAGTTTTAAAATATATTAC ACTTATTTGTTATTTGCACCAGACCATGGTTTCTTTCTTTTTCGTAAAGTTTTAAAATATATTAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:24641648..24641775 26863196 MeRIP-seq:(Medium) rs956244657 Functional Loss SNV dbSNP153 33..33 33 - - - 89560 RMVar_ID_89560 Human_SNP_ID_314034685 m1A Human chr7 - 24907047 24907047 24907047 GAGAGAATCTACACTACTGGGGGCTCTGGGAGAGGGAGTTTGGTTGGATTAATAGAGGGTGGGTA GAGAGAATCTACACTACTGGGGGCTCTGGGAGTGGGAGTTTGGTTGGATTAATAGAGGGTGGGTA T A OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:24907032..24907225 26863196 MeRIP-seq:(Medium) rs887477809 Functional Loss SNV dbSNP153 33..33 33 - - - 89561 RMVar_ID_89561 Human_SNP_ID_314034841 m1A Human chr7 - 24907754 24907754 24907754 GTGACTAATACTTTCAGGTAGCGCAAAAGGAAAGCAGAGTCCAAGAGGAAACAAACGCATTTGGG GTGACTAATACTTTCAGGTAGCGCAAAAGGAAGGCAGAGTCCAAGAGGAAACAAACGCATTTGGG T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:24907748..24907814 26863196 MeRIP-seq:(Medium) rs1481035038 Functional Loss SNV dbSNP153 33..33 33 - - - 89562 RMVar_ID_89562 Human_SNP_ID_314052374 m1A Human chr7 - 24980002 24980002 24980002 CCCCGACTCCTGCGGCCGGTGCGGGAGCTGTCAGCTGCACGTTGCGGGGGTACCGGAGAAGCCGG CCCCGACTCCTGCGGCCGGTGCGGGAGCTGTCGGCTGCACGTTGCGGGGGTACCGGAGAAGCCGG T C OSBPL3 Ensembl:ENSG00000070882 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:24979951..24980100 26863196 MeRIP-seq:(Medium) rs1041974901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18425977,Human_RBP_ID_18451519 89563 RMVar_ID_89563 Human_SNP_ID_314089294 m1A Human chr7 - 25123756 25123756 25123756 TGGAACAAAAATGATCTTTGTCGGCATTAAGAAGAAGGAAGAAAGGGCAGACTTAATAGCTTATC TGGAACAAAAATGATCTTTGTCGGCATTAAGAGGAAGGAAGAAAGGGCAGACTTAATAGCTTATC T C CYCS Ensembl:ENSG00000172115 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:25123726..25123800 26863196 MeRIP-seq:(Medium) rs11548785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_681575,Human_RBP_ID_794495,Human_RBP_ID_2040339,Human_RBP_ID_7726546,Human_RBP_ID_9403214,Human_RBP_ID_16122839,Human_RBP_ID_17664977,Human_RBP_ID_22464404,Human_RBP_ID_22834686,Human_RBP_ID_24208680,Human_RBP_ID_24549277,Human_RBP_ID_26355949,Human_RBP_ID_27111071,Human_RBP_ID_27829216 Human_Splice_Rec_850816,Human_Splice_Rec_850820,Human_Splice_Rec_850826,Human_Splice_Rec_850832 89564 RMVar_ID_89564 Human_SNP_ID_314089430 m1A Human chr7 - 25124126 25124126 25124126 AAATTTACTAAGTTGAAGCTTTCGTTTTTAGAATTAAATATGGGTGATGTTGAGAAAGGCAAGAA AAATTTACTAAGTTGAAGCTTTCGTTTTTAGAGTTAAATATGGGTGATGTTGAGAAAGGCAAGAA T C CYCS Ensembl:ENSG00000172115 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:25123730..25124715;chr7:25123951..25124715 26863196 MeRIP-seq:(Medium) rs774034189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_315657,Human_RBP_ID_4956235,Human_RBP_ID_18425979,Human_RBP_ID_23215439,Human_RBP_ID_26356321 Human_Splice_Rec_850814,Human_Splice_Rec_850818,Human_Splice_Rec_850824,Human_Splice_Rec_850830 89565 RMVar_ID_89565 Human_SNP_ID_314103808 m1A Human chr7 + 25180239 25180239 25180239 GGGCTTCCGGGCGGCGAGCGGGGCGCAGTAGGAGGCTCTTAGAGACCTCGGAGGAAACCAGCCCA GGGCTTCCGGGCGGCGAGCGGGGCGCAGTAGGCGGCTCTTAGAGACCTCGGAGGAAACCAGCCCA A C lnc-MPP6-1,lnc-MPP6-1:2 RNACentral:URS0000D57251,RNACentral:URS0000D5DAB1 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:25180189..25180316 26863196 MeRIP-seq:(Medium) rs1333166620 Functional Loss SNV dbSNP153 33..33 33 - - - 89566 RMVar_ID_89566 Human_SNP_ID_314103839 m1A Human chr7 + 25180310 25180310 25180310 CGGGACTGGCAAGAATGCGAAGAGGAACCGAGAGTGAACGGAGTGCGAGGCGCCGGGTCGGAGGC CGGGACTGGCAAGAATGCGAAGAGGAACCGAGCGTGAACGGAGTGCGAGGCGCCGGGTCGGAGGC A C lnc-MPP6-1,lnc-MPP6-1:2 RNACentral:URS0000D57251,RNACentral:URS0000D5DAB1 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:25180196..25180350 26863196 MeRIP-seq:(Medium) rs1342908730 Functional Loss SNV dbSNP153 33..33 33 - - - 89567 RMVar_ID_89567 Human_SNP_ID_314297801 m1A Human chr7 + 25950701 25950699 25950701 TTCCCGCGGACCCCGTTCGCGCACAACCTTGCACACAGTCCCCAAGACTGCTCTTCTCCCCCTCC TTCCCGCGGACCCCGTTCGCGCACAACCTTG__CACAGTCCCCAAGACTGCTCTTCTCCCCCTCC GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:25950658..25950763 26863196 MeRIP-seq:(Medium) rs1033367998 Functional Loss DEL dbSNP153 32..33 33 - - - 89568 RMVar_ID_89568 Human_SNP_ID_314297802 m1A Human chr7 + 25950701 25950701 25950701 TTCCCGCGGACCCCGTTCGCGCACAACCTTGCACACAGTCCCCAAGACTGCTCTTCTCCCCCTCC TTCCCGCGGACCCCGTTCGCGCACAACCTTGCGCACAGTCCCCAAGACTGCTCTTCTCCCCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:25950658..25950763 26863196 MeRIP-seq:(Medium) rs1344322017 Functional Loss SNV dbSNP153 33..33 33 - - - 89569 RMVar_ID_89569 Human_SNP_ID_314345785 m1A Human chr7 + 26152237 26152237 26152237 GGCCACCGCGCCGGGCTGCGGGCGGCTGGGCGAACGGGCTCGGCGCTCAGGTGGCTCCTTCTTCG GGCCACCGCGCCGGGCTGCGGGCGGCTGGGCGGACGGGCTCGGCGCTCAGGTGGCTCCTTCTTCG A G NFE2L3 Ensembl:ENSG00000050344 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:26152228..26152348;chr7:26152227..26152590 26863196 MeRIP-seq:(Medium) rs1291206256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1331574 89570 RMVar_ID_89570 Human_SNP_ID_314345786 m1A Human chr7 + 26152237 26152237 26152237 GGCCACCGCGCCGGGCTGCGGGCGGCTGGGCGAACGGGCTCGGCGCTCAGGTGGCTCCTTCTTCG GGCCACCGCGCCGGGCTGCGGGCGGCTGGGCGTACGGGCTCGGCGCTCAGGTGGCTCCTTCTTCG A T NFE2L3 Ensembl:ENSG00000050344 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:26152228..26152348;chr7:26152227..26152590 26863196 MeRIP-seq:(Medium) rs1291206256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1331574 89571 RMVar_ID_89571 Human_SNP_ID_314345790 m1A Human chr7 - 26152244 26152244 26152244 GGAGAAGCGAAGAAGGAGCCACCTGAGCGCCGAGCCCGTTCGCCCAGCCGCCCGCAGCCCGGCGC GGAGAAGCGAAGAAGGAGCCACCTGAGCGCCGTGCCCGTTCGCCCAGCCGCCCGCAGCCCGGCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:26152240..26152540 26863196 MeRIP-seq:(Medium) rs1041555989 Functional Loss SNV dbSNP153 33..33 33 - - - 89572 RMVar_ID_89572 Human_SNP_ID_314345838 m1A Human chr7 - 26152379 26152379 26152379 CCGCCCGCACCTGCCTGGAACCCAGATAAGCGAAACAATGGACCGGGGCGCGTGGCGGCCGTCGC CCGCCCGCACCTGCCTGGAACCCAGATAAGCGGAACAATGGACCGGGGCGCGTGGCGGCCGTCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:26152289..26152390 26863410 MeRIP-seq:(Medium) rs1429189417 Functional Loss SNV dbSNP153 33..33 33 - - - 89573 RMVar_ID_89573 Human_SNP_ID_314346119 m1A Human chr7 - 26152991 26152991 26152991 CGCGGGTGCCTTCTCCTCTTCCCCGGCGTCCAAGGGGCCACTCCGAGCCGCTCGGGGGTCCCCGC CGCGGGTGCCTTCTCCTCTTCCCCGGCGTCCAGGGGGCCACTCCGAGCCGCTCGGGGGTCCCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:26152889..26153040 26863410 MeRIP-seq:(Medium) rs1205695854 Functional Loss SNV dbSNP153 33..33 33 - - - 89574 RMVar_ID_89574 Human_SNP_ID_314346152 m1A Human chr7 + 26153056 26153056 26153056 GAACCGACGGCTCAGGTGCCGGACGCTGGCGGATGTGCGAGCGAGGTAGGTGCAGAGCGGGAAGC GAACCGACGGCTCAGGTGCCGGACGCTGGCGGTTGTGCGAGCGAGGTAGGTGCAGAGCGGGAAGC A T NFE2L3 Ensembl:ENSG00000050344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:26152889..26177964 26863196 MeRIP-seq:(Medium) rs1350747557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_851085 89575 RMVar_ID_89575 Human_SNP_ID_314359764 m1A Human chr7 - 26192340 26192340 26192340 ATTTTTTTTTTACTCTTTACTTCTGTTGAAACAGGCTTCACTGTATAAATAGGAGAGGATGAGAG ATTTTTTTTTTACTCTTTACTTCTGTTGAAACGGGCTTCACTGTATAAATAGGAGAGGATGAGAG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:26192301..26192350 26863196 MeRIP-seq:(Medium) rs111456264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86984,Human_RBP_ID_681694,Human_RBP_ID_1685381,Human_RBP_ID_2040445,Human_RBP_ID_3082684,Human_RBP_ID_7727056,Human_RBP_ID_8146965,Human_RBP_ID_9209543,Human_RBP_ID_10373425,Human_RBP_ID_16124241,Human_RBP_ID_17048340,Human_RBP_ID_18880857,Human_RBP_ID_21561114,Human_RBP_ID_22834768,Human_RBP_ID_23075458,Human_RBP_ID_24516057,Human_RBP_ID_26095372,Human_RBP_ID_27111198,Human_RBP_ID_27767155 RMVar_hsa_circ_25234,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135 89576 RMVar_ID_89576 Human_SNP_ID_314359824 m1A Human chr7 + 26192477 26192477 26192477 AGCTATGTCTCCCAAGATAATAATAATTGTAAAACTCAAAAGCTACTTACCCATGGCAAATAGGA AGCTATGTCTCCCAAGATAATAATAATTGTAAGACTCAAAAGCTACTTACCCATGGCAAATAGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:26192473..26195764 32194978 MeRIP-seq:(Medium) rs1276616644 Functional Loss SNV dbSNP153 33..33 33 - - - 89577 RMVar_ID_89577 Human_SNP_ID_314359879 m1A Human chr7 - 26192576 26192576 26192576 TTGTTTTCTCTTGCTGTTCCAACAATTATAGGAAACTATGGTCCAGGAGGCAGTGGAGGAAGTGG TTGTTTTCTCTTGCTGTTCCAACAATTATAGGGAACTATGGTCCAGGAGGCAGTGGAGGAAGTGG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr7:26192463..26192613;chr7:26192526..26192600 26863196 MeRIP-seq:(Medium) rs1416641470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86985,Human_RBP_ID_681716,Human_RBP_ID_844385,Human_RBP_ID_1051604,Human_RBP_ID_1331601,Human_RBP_ID_3082699,Human_RBP_ID_5152921,Human_RBP_ID_7727066,Human_RBP_ID_9209555,Human_RBP_ID_9444326,Human_RBP_ID_16124269,Human_RBP_ID_17665249,Human_RBP_ID_22463035,Human_RBP_ID_22834784,Human_RBP_ID_23080525,Human_RBP_ID_24209008,Human_RBP_ID_26095391,Human_RBP_ID_26355950,Human_RBP_ID_27767164 Human_Splice_Rec_851110,Human_Splice_Rec_851111,Human_Splice_Rec_851134,Human_Splice_Rec_851135,Human_Splice_Rec_851154,Human_Splice_Rec_851155,Human_Splice_Rec_851176,Human_Splice_Rec_851177,Human_Splice_Rec_851196,Human_Splice_Rec_851214,Human_Splice_Rec_851215,Human_Splice_Rec_851232,Human_Splice_Rec_851233 Human_miRNA_ID_2968231 RMVar_hsa_circ_84857,RMVar_hsa_circ_25234,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_353187,RMVar_hsa_circ_128060,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216 89578 RMVar_ID_89578 Human_SNP_ID_314360362 m1A Human chr7 - 26193625 26193625 26193625 AAGAGGAGGATATGGTGGTGGAGGACCTGGATATGGCAACCAGGGTGGGGGCTACGGAGGTGGTT AAGAGGAGGATATGGTGGTGGAGGACCTGGATGTGGCAACCAGGGTGGGGGCTACGGAGGTGGTT T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:26193174..26193797 26863196 MeRIP-seq:(Medium) rs745389971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84110,Human_RBP_ID_253292,Human_RBP_ID_793272,Human_RBP_ID_844467,Human_RBP_ID_1051621,Human_RBP_ID_1143752,Human_RBP_ID_1685417,Human_RBP_ID_2040463,Human_RBP_ID_3082728,Human_RBP_ID_4936416,Human_RBP_ID_5628271,Human_RBP_ID_7727114,Human_RBP_ID_8665200,Human_RBP_ID_8910392,Human_RBP_ID_9209573,Human_RBP_ID_9403223,Human_RBP_ID_9444327,Human_RBP_ID_10347196,Human_RBP_ID_16124333,Human_RBP_ID_18098035,Human_RBP_ID_19020632,Human_RBP_ID_22464410,Human_RBP_ID_22834798,Human_RBP_ID_23080528,Human_RBP_ID_23120480,Human_RBP_ID_23139984,Human_RBP_ID_24209028,Human_RBP_ID_24549101,Human_RBP_ID_26137119,Human_RBP_ID_26355955,Human_RBP_ID_27111213,Human_RBP_ID_27356058,Human_RBP_ID_27530736,Human_RBP_ID_27767187,Human_RBP_ID_27829221,Human_RBP_ID_27842870 Human_Splice_Rec_851106,Human_Splice_Rec_851107,Human_Splice_Rec_851130,Human_Splice_Rec_851131,Human_Splice_Rec_851150,Human_Splice_Rec_851151,Human_Splice_Rec_851172,Human_Splice_Rec_851173,Human_Splice_Rec_851192,Human_Splice_Rec_851193,Human_Splice_Rec_851210,Human_Splice_Rec_851211,Human_Splice_Rec_851228,Human_Splice_Rec_851229 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_68397,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_244220,RMVar_hsa_circ_378464,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244221,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222 89579 RMVar_ID_89579 Human_SNP_ID_314360381 m1A Human chr7 - 26193688 26193688 26193688 TTACTTAAAGGCTTATTTTATAATAGGTGGCAATTTTGGAGGTAGCCCCGGTTATGGAGGAGGAA TTACTTAAAGGCTTATTTTATAATAGGTGGCAGTTTTGGAGGTAGCCCCGGTTATGGAGGAGGAA T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:26193336..26193782 26863196 MeRIP-seq:(Medium) rs1292889600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14354,Human_RBP_ID_84110,Human_RBP_ID_253292,Human_RBP_ID_681748,Human_RBP_ID_844467,Human_RBP_ID_1051621,Human_RBP_ID_1070150,Human_RBP_ID_3082730,Human_RBP_ID_7727115,Human_RBP_ID_8910395,Human_RBP_ID_9403226,Human_RBP_ID_16124336,Human_RBP_ID_17425119,Human_RBP_ID_18098035,Human_RBP_ID_19020635,Human_RBP_ID_22463912,Human_RBP_ID_23075501,Human_RBP_ID_23120482,Human_RBP_ID_24549102,Human_RBP_ID_26095456,Human_RBP_ID_26356337,Human_RBP_ID_26724167,Human_RBP_ID_27767188,Human_RBP_ID_27829222,Human_RBP_ID_27842871 Human_Splice_Rec_851106,Human_Splice_Rec_851130,Human_Splice_Rec_851150,Human_Splice_Rec_851172,Human_Splice_Rec_851192,Human_Splice_Rec_851210,Human_Splice_Rec_851228 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_68397,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_244226 89580 RMVar_ID_89580 Human_SNP_ID_314361522 m1A Human chr7 - 26195736 26195736 26195736 GAGTTTTTAAACATTTTATATTAGTGTCTATAAATGGCTTGGGTGATAGTGGTCCAGTTATTTCT GAGTTTTTAAACATTTTATATTAGTGTCTATACATGGCTTGGGTGATAGTGGTCCAGTTATTTCT T G HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:26195734..26195999 26863196 MeRIP-seq:(Medium) rs1046351818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_681756,Human_RBP_ID_7727161,Human_RBP_ID_16124468,Human_RBP_ID_23075535,Human_RBP_ID_24516090,Human_RBP_ID_26095536 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_244226 89581 RMVar_ID_89581 Human_SNP_ID_314361539 m1A Human chr7 + 26195764 26195764 26195764 CCATTTATAGACACTAATATAAAATGTTTAAAAACTCAAAATATAAATGAAGTAAATATACGATA CCATTTATAGACACTAATATAAAATGTTTAAAGACTCAAAATATAAATGAAGTAAATATACGATA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:26195762..26195973 26863196 MeRIP-seq:(Medium) rs572767559 Functional Loss SNV dbSNP153 33..33 33 - - - 89582 RMVar_ID_89582 Human_SNP_ID_314361603 m1A Human chr7 + 26195828 26195828 26195828 ATAGTTAAGTATTAGTCACATAAACAAACCAAAACGTAGAGGAAAACTGACCTCCAGGTCCTCCT ATAGTTAAGTATTAGTCACATAAACAAACCAAGACGTAGAGGAAAACTGACCTCCAGGTCCTCCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:26195826..26195900;chr7:26195826..26196675;chr7:26195826..26197027;chr7:26195826..26196679 26863196 MeRIP-seq:(Medium) rs183451681 Functional Loss SNV dbSNP153 33..33 33 - - - 89583 RMVar_ID_89583 Human_SNP_ID_314361633 m1A Human chr7 - 26195893 26195893 26195893 TTTTGGCCCCTAACAGATGGATATGGCAGTGGACGTGGATTTGGGGATGGCTATAATGGGTATGG TTTTGGCCCCTAACAGATGGATATGGCAGTGGGCGTGGATTTGGGGATGGCTATAATGGGTATGG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:26195815..26195950 26863410 MeRIP-seq:(Medium) rs199650578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84112,Human_RBP_ID_253295,Human_RBP_ID_681757,Human_RBP_ID_843597,Human_RBP_ID_1051625,Human_RBP_ID_1220971,Human_RBP_ID_1685439,Human_RBP_ID_2040485,Human_RBP_ID_3124440,Human_RBP_ID_3842098,Human_RBP_ID_5219346,Human_RBP_ID_5622856,Human_RBP_ID_7727169,Human_RBP_ID_8665211,Human_RBP_ID_8910397,Human_RBP_ID_16124473,Human_RBP_ID_18098039,Human_RBP_ID_18451529,Human_RBP_ID_18880879,Human_RBP_ID_22515637,Human_RBP_ID_23080531,Human_RBP_ID_23120483,Human_RBP_ID_23139986,Human_RBP_ID_24209041,Human_RBP_ID_24389037,Human_RBP_ID_26131031,Human_RBP_ID_26355956,Human_RBP_ID_27829224 Human_Splice_Rec_851104,Human_Splice_Rec_851105,Human_Splice_Rec_851128,Human_Splice_Rec_851129,Human_Splice_Rec_851149,Human_Splice_Rec_851170,Human_Splice_Rec_851171,Human_Splice_Rec_851190,Human_Splice_Rec_851191,Human_Splice_Rec_851208,Human_Splice_Rec_851209,Human_Splice_Rec_851226,Human_Splice_Rec_851227,Human_Splice_Rec_851240 Human_miRNA_ID_2968232,Human_miRNA_ID_2968233 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_61069,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_266045,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_244226,RMVar_hsa_circ_356480,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244227,RMVar_hsa_circ_244228 89584 RMVar_ID_89584 Human_SNP_ID_314361635 m1A Human chr7 + 26195896 26195896 26195896 TACCCATTATAGCCATCCCCAAATCCACGTCCACTGCCATATCCATCTGTTAGGGGCCAAAAAAA TACCCATTATAGCCATCCCCAAATCCACGTCCCCTGCCATATCCATCTGTTAGGGGCCAAAAAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:26195826..26195925 32194978 MeRIP-seq:(Medium) rs761653754 Functional Loss SNV dbSNP153 33..33 33 - - - 89585 RMVar_ID_89585 Human_SNP_ID_314361636 m1A Human chr7 + 26195896 26195896 26195896 TACCCATTATAGCCATCCCCAAATCCACGTCCACTGCCATATCCATCTGTTAGGGGCCAAAAAAA TACCCATTATAGCCATCCCCAAATCCACGTCCGCTGCCATATCCATCTGTTAGGGGCCAAAAAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:26195826..26195925 32194978 MeRIP-seq:(Medium) rs761653754 Functional Loss SNV dbSNP153 33..33 33 - - - 89586 RMVar_ID_89586 Human_SNP_ID_314361640 m1A Human chr7 - 26195903 26195903 26195903 CGTAATCTTTTTTTGGCCCCTAACAGATGGATATGGCAGTGGACGTGGATTTGGGGATGGCTATA CGTAATCTTTTTTTGGCCCCTAACAGATGGATGTGGCAGTGGACGTGGATTTGGGGATGGCTATA T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:26195826..26195925 26863196 MeRIP-seq:(Medium) rs1193509264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84112,Human_RBP_ID_253295,Human_RBP_ID_681758,Human_RBP_ID_843597,Human_RBP_ID_1051625,Human_RBP_ID_1685439,Human_RBP_ID_4936423,Human_RBP_ID_7727171,Human_RBP_ID_8910397,Human_RBP_ID_16124473,Human_RBP_ID_21480603,Human_RBP_ID_22108692,Human_RBP_ID_22515637,Human_RBP_ID_22834809,Human_RBP_ID_23080531,Human_RBP_ID_23120483,Human_RBP_ID_24209041,Human_RBP_ID_24389037,Human_RBP_ID_26095543,Human_RBP_ID_26355957,Human_RBP_ID_27829224 Human_Splice_Rec_851104,Human_Splice_Rec_851105,Human_Splice_Rec_851128,Human_Splice_Rec_851129,Human_Splice_Rec_851149,Human_Splice_Rec_851170,Human_Splice_Rec_851171,Human_Splice_Rec_851190,Human_Splice_Rec_851191,Human_Splice_Rec_851208,Human_Splice_Rec_851209,Human_Splice_Rec_851226,Human_Splice_Rec_851227,Human_Splice_Rec_851240 Human_miRNA_ID_2968232,Human_miRNA_ID_2968233 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_61069,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_266045,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_244226,RMVar_hsa_circ_356480,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244227,RMVar_hsa_circ_244228 89587 RMVar_ID_89587 Human_SNP_ID_314361641 m1A Human chr7 - 26195911 26195911 26195911 ATAGTAAACGTAATCTTTTTTTGGCCCCTAACAGATGGATATGGCAGTGGACGTGGATTTGGGGA ATAGTAAACGTAATCTTTTTTTGGCCCCTAACTGATGGATATGGCAGTGGACGTGGATTTGGGGA T A HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:26195793..26195947 26863410 MeRIP-seq:(Medium) rs113435013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84112,Human_RBP_ID_954275,Human_RBP_ID_16124473,Human_RBP_ID_22834809,Human_RBP_ID_24389037,Human_RBP_ID_26095543 Human_Splice_Rec_851105,Human_Splice_Rec_851129,Human_Splice_Rec_851149,Human_Splice_Rec_851171,Human_Splice_Rec_851191,Human_Splice_Rec_851209,Human_Splice_Rec_851227 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_366603,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_61069,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_356480,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244227,RMVar_hsa_circ_244228 89588 RMVar_ID_89588 Human_SNP_ID_314361919 m1A Human chr7 + 26196378 26196378 26196378 CATATTTAAAATAAAAGCACACTCATCCTTTAAACACGTAGAACTTGAAACTCACCAGATCCTCC CATATTTAAAATAAAAGCACACTCATCCTTTATACACGTAGAACTTGAAACTCACCAGATCCTCC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:26196370..26196544 26863410 MeRIP-seq:(Medium) rs1020671316 Functional Loss SNV dbSNP153 33..33 33 - - - 89589 RMVar_ID_89589 Human_SNP_ID_314362025 m1A Human chr7 - 26196558 26196555 26196558 CAGGAAGTTCAGAGTTCTAGGAGTGGAAGAGGAGGTAATTTTAATTCTGTTTCTTCTTTATTTTT CAGGAAGTTCAGAGTTCTAGGAGTGGAAGAGG___TAATTTTAATTCTGTTTCTTCTTTATTTTT ACCT A HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:26196551..26196575 26863196 MeRIP-seq:(Medium) rs902316320 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_253297,Human_RBP_ID_681764,Human_RBP_ID_793280,Human_RBP_ID_844469,Human_RBP_ID_2040495,Human_RBP_ID_3842103,Human_RBP_ID_5622860,Human_RBP_ID_7727187,Human_RBP_ID_8271882,Human_RBP_ID_8665215,Human_RBP_ID_16124519,Human_RBP_ID_23075554,Human_RBP_ID_24209052,Human_RBP_ID_26137165,Human_RBP_ID_26356347 Human_Splice_Rec_851101,Human_Splice_Rec_851125,Human_Splice_Rec_851167,Human_Splice_Rec_851187,Human_Splice_Rec_851205,Human_Splice_Rec_851223,Human_Splice_Rec_851237 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_374972,RMVar_hsa_circ_366603,RMVar_hsa_circ_244219,RMVar_hsa_circ_338242,RMVar_hsa_circ_61069,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244229,RMVar_hsa_circ_64666,RMVar_hsa_circ_244228,RMVar_hsa_circ_65130,RMVar_hsa_circ_350895,RMVar_hsa_circ_353579,RMVar_hsa_circ_373388,RMVar_hsa_circ_244230 89590 RMVar_ID_89590 Human_SNP_ID_314362036 m1A Human chr7 + 26196603 26196603 26196603 CTAGAACTCTGAACTTCCTGCATTTCTTGTCTAGACAAAGCCTTTCTTACTTCTGCATTATGACC CTAGAACTCTGAACTTCCTGCATTTCTTGTCTGGACAAAGCCTTTCTTACTTCTGCATTATGACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:26195863..26196650 32194978 MeRIP-seq:(Medium) rs1395171310 Functional Loss SNV dbSNP153 33..33 33 - - - 89591 RMVar_ID_89591 Human_SNP_ID_314362607 m1A Human chr7 - 26197725 26197725 26197725 ATTGAAATGGTATTTTCCTTTGCAGAGAGAAAAGGAACAGTTCCGTAAGCTCTTTATTGGTGGCT ATTGAAATGGTATTTTCCTTTGCAGAGAGAAAGGGAACAGTTCCGTAAGCTCTTTATTGGTGGCT T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:26197601..26197756 26863196 MeRIP-seq:(Medium) rs751281272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84118,Human_RBP_ID_253303,Human_RBP_ID_681795,Human_RBP_ID_793285,Human_RBP_ID_1685478,Human_RBP_ID_2040509,Human_RBP_ID_5401459,Human_RBP_ID_7727227,Human_RBP_ID_8910418,Human_RBP_ID_9209602,Human_RBP_ID_16124572,Human_RBP_ID_19134735,Human_RBP_ID_22464413,Human_RBP_ID_22555121,Human_RBP_ID_22620092,Human_RBP_ID_22685310,Human_RBP_ID_24562932,Human_RBP_ID_26095637,Human_RBP_ID_27767206,Human_RBP_ID_27843079 Human_Splice_Rec_851094,Human_Splice_Rec_851118,Human_Splice_Rec_851140,Human_Splice_Rec_851160,Human_Splice_Rec_851198 Human_miRNA_ID_147408 RMVar_hsa_circ_80785,RMVar_hsa_circ_84857,RMVar_hsa_circ_352214,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_338242,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_363221,RMVar_hsa_circ_351112,RMVar_hsa_circ_244229,RMVar_hsa_circ_64666,RMVar_hsa_circ_244228,RMVar_hsa_circ_350895,RMVar_hsa_circ_373388,RMVar_hsa_circ_56470,RMVar_hsa_circ_316200,RMVar_hsa_circ_333470,RMVar_hsa_circ_244231 89592 RMVar_ID_89592 Human_SNP_ID_314362609 m1A Human chr7 - 26197732 26197732 26197732 AATAAAAATTGAAATGGTATTTTCCTTTGCAGAGAGAAAAGGAACAGTTCCGTAAGCTCTTTATT AATAAAAATTGAAATGGTATTTTCCTTTGCAGCGAGAAAAGGAACAGTTCCGTAAGCTCTTTATT T G HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:26197699..26197796 26863196 MeRIP-seq:(Medium) rs533527065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84118,Human_RBP_ID_1685478,Human_RBP_ID_2040509,Human_RBP_ID_5401459,Human_RBP_ID_16124572,Human_RBP_ID_22464413,Human_RBP_ID_22555121,Human_RBP_ID_22620092,Human_RBP_ID_22685310,Human_RBP_ID_24562932,Human_RBP_ID_26095637,Human_RBP_ID_27843079 Human_Splice_Rec_851094,Human_Splice_Rec_851118,Human_Splice_Rec_851140,Human_Splice_Rec_851160,Human_Splice_Rec_851198 RMVar_hsa_circ_80785,RMVar_hsa_circ_84857,RMVar_hsa_circ_352214,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_338242,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_363221,RMVar_hsa_circ_351112,RMVar_hsa_circ_244229,RMVar_hsa_circ_64666,RMVar_hsa_circ_244228,RMVar_hsa_circ_350895,RMVar_hsa_circ_373388,RMVar_hsa_circ_56470,RMVar_hsa_circ_316200,RMVar_hsa_circ_333470,RMVar_hsa_circ_244231 89593 RMVar_ID_89593 Human_SNP_ID_314363751 m1A Human chr7 - 26199881 26199880 26199881 ATTGCGTTCGGAAGCCACACCGAAGAGCGGGGAGGGGGGGTGCTCCGGGTTTGCGGGCCCGGTTT ATTGCGTTCGGAAGCCACACCGAAGAGCGGGG_GGGGGGGTGCTCCGGGTTTGCGGGCCCGGTTT CT C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:26199880..26199981 32194978 MeRIP-seq:(Medium) rs1207917657 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_285890,Human_RBP_ID_844199,Human_RBP_ID_1114267,Human_RBP_ID_7727306,Human_RBP_ID_16286276 RMVar_hsa_circ_80785,RMVar_hsa_circ_84857,RMVar_hsa_circ_244215,RMVar_hsa_circ_244225 89594 RMVar_ID_89594 Human_SNP_ID_314364229 m1A Human chr7 - 26200623 26200623 26200623 CCGGTTCGTGTTCGTCCGCGGAGATCTCTCTCATCTCGCTCGGCTGCGGGAAATCGGGCTGAAGC CCGGTTCGTGTTCGTCCGCGGAGATCTCTCTCCTCTCGCTCGGCTGCGGGAAATCGGGCTGAAGC T G HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr7:26200291..26200750;chr7:26200323..26200750;chr7:26200251..26200775;chr7:26200551..26200800 26863196 MeRIP-seq:(Medium) rs1562731630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84124,Human_RBP_ID_253309,Human_RBP_ID_681799,Human_RBP_ID_793294,Human_RBP_ID_1051643,Human_RBP_ID_1220991,Human_RBP_ID_1398357,Human_RBP_ID_1685523,Human_RBP_ID_2040544,Human_RBP_ID_3842144,Human_RBP_ID_4956238,Human_RBP_ID_5429918,Human_RBP_ID_5452257,Human_RBP_ID_5479458,Human_RBP_ID_5513961,Human_RBP_ID_7727347,Human_RBP_ID_8665270,Human_RBP_ID_8910419,Human_RBP_ID_9209626,Human_RBP_ID_9337090,Human_RBP_ID_9403243,Human_RBP_ID_10347358,Human_RBP_ID_16124808,Human_RBP_ID_17712875,Human_RBP_ID_18098064,Human_RBP_ID_18451539,Human_RBP_ID_18880939,Human_RBP_ID_19134738,Human_RBP_ID_22321601,Human_RBP_ID_22463913,Human_RBP_ID_22515663,Human_RBP_ID_22834874,Human_RBP_ID_23075701,Human_RBP_ID_24209124,Human_RBP_ID_26137251,Human_RBP_ID_27111283,Human_RBP_ID_27356091,Human_RBP_ID_27530760,Human_RBP_ID_27767211 Human_Splice_Rec_851093,Human_Splice_Rec_851115,Human_Splice_Rec_851137,Human_Splice_Rec_851157,Human_Splice_Rec_851197 Human_miRNA_ID_2064895,Human_miRNA_ID_2702766,Human_miRNA_ID_2934072 RMVar_hsa_circ_44173,RMVar_hsa_circ_80785,RMVar_hsa_circ_84857,RMVar_hsa_circ_244215,RMVar_hsa_circ_244225,RMVar_hsa_circ_101325,RMVar_hsa_circ_244233 89595 RMVar_ID_89595 Human_SNP_ID_314364987 m1A Human chr7 + 26201807 26201807 26201807 AGGGCCGGAGACGCTGCAGACCCGCGACCCGGAGCAGCTCGGAGGCGGTGAAGTCGGTGGCTTTC AGGGCCGGAGACGCTGCAGACCCGCGACCCGGTGCAGCTCGGAGGCGGTGAAGTCGGTGGCTTTC A T CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:26201478..26201985;chr7:26201726..26201922;chr7:26201726..26201890 26863196 MeRIP-seq:(Medium) rs1184243362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254223,Human_RBP_ID_4936521,Human_RBP_ID_16124827,Human_RBP_ID_19136134,Human_RBP_ID_22110697,Human_RBP_ID_23080054,Human_RBP_ID_26356353 Human_Splice_Rec_851251,Human_Splice_Rec_851267 89596 RMVar_ID_89596 Human_SNP_ID_314364996 m1A Human chr7 - 26201823 26201820 26201823 GAGAGCTAGAGAGAAGGAAAGCCACCGACTTCACCGCCTCCGAGCTGCTCCGGGTCGCGGGTCTG GAGAGCTAGAGAGAAGGAAAGCCACCGACTTC___GCCTCCGAGCTGCTCCGGGTCGCGGGTCTG CGGT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:26201510..26202091 26863410 MeRIP-seq:(Medium) rs1243927384 Functional Loss DEL dbSNP153 33..35 33 - - - 89597 RMVar_ID_89597 Human_SNP_ID_314364999 m1A Human chr7 - 26201823 26201823 26201823 GAGAGCTAGAGAGAAGGAAAGCCACCGACTTCACCGCCTCCGAGCTGCTCCGGGTCGCGGGTCTG GAGAGCTAGAGAGAAGGAAAGCCACCGACTTCTCCGCCTCCGAGCTGCTCCGGGTCGCGGGTCTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:26201510..26202091 26863410 MeRIP-seq:(Medium) rs1373421864 Functional Loss SNV dbSNP153 33..33 33 - - - 89598 RMVar_ID_89598 Human_SNP_ID_314366977 m1A Human chr7 + 26206451 26206451 26206451 GAGCCTGAAGAATTTGTCGTGGAAAAAGTACTAGATCGACGTGTAGTGAATGGGAAAGTGGAATA GAGCCTGAAGAATTTGTCGTGGAAAAAGTACTGGATCGACGTGTAGTGAATGGGAAAGTGGAATA A G CBX3 Ensembl:ENSG00000122565 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:26206306..26206525 26863196 MeRIP-seq:(Medium) rs775850433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253287,Human_RBP_ID_681817,Human_RBP_ID_957273,Human_RBP_ID_2040559,Human_RBP_ID_3082894,Human_RBP_ID_3842160,Human_RBP_ID_9403251,Human_RBP_ID_16125044,Human_RBP_ID_24209153,Human_RBP_ID_24548886,Human_RBP_ID_26356355,Human_RBP_ID_27111302,Human_RBP_ID_27830232 Human_Splice_Rec_851244,Human_Splice_Rec_851245,Human_Splice_Rec_851254,Human_Splice_Rec_851255,Human_Splice_Rec_851264,Human_Splice_Rec_851265,Human_Splice_Rec_851270,Human_Splice_Rec_851271,Human_Splice_Rec_851278,Human_Splice_Rec_851279,Human_Splice_Rec_851283,Human_Splice_Rec_851285 RMVar_hsa_circ_48144,RMVar_hsa_circ_59959,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639,RMVar_hsa_circ_105553,RMVar_hsa_circ_285734,RMVar_hsa_circ_244234,RMVar_hsa_circ_5004,RMVar_hsa_circ_244235 89599 RMVar_ID_89599 Human_SNP_ID_314390145 m1A Human chr7 - 26291984 26291984 26291984 CTCAAAGGCGCGCGGCGGCAGCGGCGGCGGCGAGCGCCCAGGAGCGCACACGAGCGCAGCCCCGC CTCAAAGGCGCGCGGCGGCAGCGGCGGCGGCGGGCGCCCAGGAGCGCACACGAGCGCAGCCCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:26291936..26292101 26863196 MeRIP-seq:(Medium) rs942003914 Functional Loss SNV dbSNP153 33..33 33 - - - 89600 RMVar_ID_89600 Human_SNP_ID_314578771 m1A Human chr7 + 27096607 27096607 27096607 GGGGCTGTGAGGAGCGCATAGAACCGTGGTGGAGGGCGAGGCTGGGCCACCGGCTCTTCAAGCTC GGGGCTGTGAGGAGCGCATAGAACCGTGGTGGGGGGCGAGGCTGGGCCACCGGCTCTTCAAGCTC A G HOTAIRM1 Ensembl:ENSG00000233429 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:27096601..27096742 26863196 MeRIP-seq:(Medium) rs1444780343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5625857 89601 RMVar_ID_89601 Human_SNP_ID_314582756 m1A Human chr7 + 27110236 27110236 27110236 AGCAGGGGGCTCTTGGCCGCGTTGGCAGGGGTAGGGTTGTTGCTGGCATTCTGAGGAGGGGAGGC AGCAGGGGGCTCTTGGCCGCGTTGGCAGGGGTTGGGTTGTTGCTGGCATTCTGAGGAGGGGAGGC A T HOXA-AS2 Ensembl:ENSG00000253552 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:27110186..27110453 26863196 MeRIP-seq:(Medium) rs773255204 Functional Loss SNV dbSNP153 33..33 33 - - - 89602 RMVar_ID_89602 Human_SNP_ID_314582763 m1A Human chr7 - 27110247 27110247 27110247 CTCCCTCTTCTGCCTCCCCTCCTCAGAATGCCAGCAACAACCCTACCCCTGCCAACGCGGCCAAG CTCCCTCTTCTGCCTCCCCTCCTCAGAATGCCGGCAACAACCCTACCCCTGCCAACGCGGCCAAG T C HOXA3 Ensembl:ENSG00000105997 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:27110196..27110417 26863196 MeRIP-seq:(Medium) rs1020839960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134802,Human_RBP_ID_18959971,Human_RBP_ID_26137308 Human_miRNA_ID_728075 89603 RMVar_ID_89603 Human_SNP_ID_314582841 m1A Human chr7 - 27110369 27110369 27110369 CCAGCCTCCAAGCCTGGGAGAGCCGCCCCTGCACCCGCCGCCGCCCCAGGCCGCGCCCCCTGCCC CCAGCCTCCAAGCCTGGGAGAGCCGCCCCTGCCCCCGCCGCCGCCCCAGGCCGCGCCCCCTGCCC T G HOXA3 Ensembl:ENSG00000105997 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:27110276..27110375 26863410 MeRIP-seq:(Medium) rs1477274540 Functional Loss SNV dbSNP153 33..33 33 - - - 89604 RMVar_ID_89604 Human_SNP_ID_314583719 m1A Human chr7 + 27113656 27113656 27113656 CCTTAACTTCTGACGAGCGCAGGCTCGGGCTCAGGCTCCGACACGGGCTCTGGCCCCCGGCCTGG CCTTAACTTCTGACGAGCGCAGGCTCGGGCTCCGGCTCCGACACGGGCTCTGGCCCCCGGCCTGG A C HOXA-AS2 Ensembl:ENSG00000253552 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:27110744..27113825 26863196 MeRIP-seq:(Medium) rs1225779692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5626081 89605 RMVar_ID_89605 Human_SNP_ID_314588047 m1A Human chr7 - 27130061 27130061 27130061 CGGGAGGTGGGCCGGGGCTGGGCCTGGGTTCGAGGGTCGGGGTCAGGAGGGAGAGGCTCAGGGGA CGGGAGGTGGGCCGGGGCTGGGCCTGGGTTCGCGGGTCGGGGTCAGGAGGGAGAGGCTCAGGGGA T G HOXA3,HOXA4,AC004080.6 Ensembl:ENSG00000105997,Ensembl:ENSG00000197576,Ensembl:ENSG00000273433 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:27130010..27130075 26863196 MeRIP-seq:(Medium) rs1455755157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955391,Human_RBP_ID_5403860,Human_RBP_ID_27111649 89606 RMVar_ID_89606 Human_SNP_ID_314595251 m1A Human chr7 + 27154507 27154507 27154507 CGGGTCTGGGAGGGTGGTGCTGGGTGTCTGCCAGTGTTGGGATACATAGGGACTTCCTGGGAATG CGGGTCTGGGAGGGTGGTGCTGGGTGTCTGCCTGTGTTGGGATACATAGGGACTTCCTGGGAATG A T HOXA-AS3 Ensembl:ENSG00000254369 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:27154457..27154815 26863196 MeRIP-seq:(Medium) rs186915437 Functional Loss SNV dbSNP153 33..33 33 - - - 89607 RMVar_ID_89607 Human_SNP_ID_314598842 m1A Human chr7 - 27165304 27165304 27165304 AGGCGGCGACGCTGGCCGAGCACCCCGACTTCAGCCCGTGCAGCTTCCAGTCCAAGGCGACGGTG AGGCGGCGACGCTGGCCGAGCACCCCGACTTCCGCCCGTGCAGCTTCCAGTCCAAGGCGACGGTG T G AC004080.3,HOXA9 Ensembl:ENSG00000257184,Ensembl:ENSG00000078399 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:27165151..27165500 26863410 MeRIP-seq:(Medium) rs758548883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1685736,Human_RBP_ID_4962591,Human_RBP_ID_18881184 Human_miRNA_ID_1980435 RMVar_hsa_circ_118571,RMVar_hsa_circ_244242 89608 RMVar_ID_89608 Human_SNP_ID_314598843 m1A Human chr7 + 27165306 27165306 27165306 CCGTCGCCTTGGACTGGAAGCTGCACGGGCTGAAGTCGGGGTGCTCGGCCAGCGTCGCCGCCTGC CCGTCGCCTTGGACTGGAAGCTGCACGGGCTGCAGTCGGGGTGCTCGGCCAGCGTCGCCGCCTGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:27165257..27165357 32194978 MeRIP-seq:(Medium) rs1341099528 Functional Loss SNV dbSNP153 33..33 33 - - - 89609 RMVar_ID_89609 Human_SNP_ID_314604780 m1A Human chr7 - 27182343 27182343 27182343 GCTTGGGGACAGGGGCAGGAGGAAGGGGTAGGATTACTAGGTGCCCAGAATGAGGCTGCTTTCCA GCTTGGGGACAGGGGCAGGAGGAAGGGGTAGGGTTACTAGGTGCCCAGAATGAGGCTGCTTTCCA T C HOXA11 Ensembl:ENSG00000005073 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:27182294..27182400 32194978 MeRIP-seq:(Medium) rs890306552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5479497,Human_RBP_ID_7728686,Human_RBP_ID_18098420,Human_RBP_ID_27530966 89610 RMVar_ID_89610 Human_SNP_ID_314605473 m1A Human chr7 + 27184547 27184527 27184547 TTTCTCCTCTGCTGCCGCCGCCGTCTCCCGGCAGCCGCCGCCGCCGCCGCTGTCCGAACTTGAAG TTTCTCCTCTGCT____________________GCCGCCGCCGCCGCCGCTGTCCGAACTTGAAG TGCCGCCGCCGTCTCCCGGCA T HOXA11-AS Ensembl:ENSG00000240990 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:27184496..27184732 26863196 MeRIP-seq:(Medium) rs1562516006 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_5105180 89611 RMVar_ID_89611 Human_SNP_ID_314605489 m1A Human chr7 + 27184547 27184547 27184547 TTTCTCCTCTGCTGCCGCCGCCGTCTCCCGGCAGCCGCCGCCGCCGCCGCTGTCCGAACTTGAAG TTTCTCCTCTGCTGCCGCCGCCGTCTCCCGGCTGCCGCCGCCGCCGCCGCTGTCCGAACTTGAAG A T HOXA11-AS Ensembl:ENSG00000240990 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:27184496..27184732 26863196 MeRIP-seq:(Medium) rs1562516037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105180 89612 RMVar_ID_89612 Human_SNP_ID_314605662 m1A Human chr7 - 27184853 27184853 27184853 AGCTCGTGCACAGAGACTGCCTGCAGGCGCCCAGCGCGGCCGGCGTGCCTGGCGACGTGCTGGCC AGCTCGTGCACAGAGACTGCCTGCAGGCGCCCGGCGCGGCCGGCGTGCCTGGCGACGTGCTGGCC T C HOXA11 Ensembl:ENSG00000005073 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:27184804..27184891 26863196 MeRIP-seq:(Medium) rs1562516282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24209825 89613 RMVar_ID_89613 Human_SNP_ID_314607592 m1A Human chr7 - 27191355 27191355 27191355 GGGTGTGTAGGGGAGGAGGGCTGGATGGGGTGATGGCTCTTCTCAAGCCTGGAATGTGAGCCAAC GGGTGTGTAGGGGAGGAGGGCTGGATGGGGTGGTGGCTCTTCTCAAGCCTGGAATGTGAGCCAAC T C AC004080.2 Ensembl:ENSG00000253508 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:27191304..27191475 26863196 MeRIP-seq:(Medium) rs1254571872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1144595 89614 RMVar_ID_89614 Human_SNP_ID_314690327 m1A Human chr7 - 27531254 27531254 27531254 CAAGTGACACTTATAATCCTGTACCTGGAGTGATGGATGGCGTTCCCTCGGCTAATAACTATCAG CAAGTGACACTTATAATCCTGTACCTGGAGTGGTGGATGGCGTTCCCTCGGCTAATAACTATCAG T C HIBADH Ensembl:ENSG00000106049 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:27526034..27531348 32194978 MeRIP-seq:(Medium) rs1032507621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682362,Human_RBP_ID_4938291 Human_Splice_Rec_851958,Human_Splice_Rec_851959,Human_Splice_Rec_851970,Human_Splice_Rec_851971,Human_Splice_Rec_851982 RMVar_hsa_circ_302262,RMVar_hsa_circ_378984,RMVar_hsa_circ_355672 89615 RMVar_ID_89615 Human_SNP_ID_314690328 m1A Human chr7 - 27531254 27531254 27531254 CAAGTGACACTTATAATCCTGTACCTGGAGTGATGGATGGCGTTCCCTCGGCTAATAACTATCAG CAAGTGACACTTATAATCCTGTACCTGGAGTGCTGGATGGCGTTCCCTCGGCTAATAACTATCAG T G HIBADH Ensembl:ENSG00000106049 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:27526034..27531348 32194978 MeRIP-seq:(Medium) rs1032507621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682362,Human_RBP_ID_4938291 Human_Splice_Rec_851958,Human_Splice_Rec_851959,Human_Splice_Rec_851970,Human_Splice_Rec_851971,Human_Splice_Rec_851982 RMVar_hsa_circ_302262,RMVar_hsa_circ_378984,RMVar_hsa_circ_355672 89616 RMVar_ID_89616 Human_SNP_ID_314719605 m1A Human chr7 - 27649602 27649602 27649602 GTGTGTTCTAGGTCAGTGGCTTCAAAGACTCCAGTTGGATTCATTGGACTGGGCAACATGGGGAA GTGTGTTCTAGGTCAGTGGCTTCAAAGACTCCGGTTGGATTCATTGGACTGGGCAACATGGGGAA T C HIBADH Ensembl:ENSG00000106049 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr7:27649551..27649680;chr7:27649535..27662699 26863196,32194978 MeRIP-seq:(Medium) rs1211042418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682407,Human_RBP_ID_4938333,Human_RBP_ID_9209794,Human_RBP_ID_16128731,Human_RBP_ID_22686755,Human_RBP_ID_26097534 Human_Splice_Rec_851948,Human_Splice_Rec_851984 Human_miRNA_ID_2656708 RMVar_hsa_circ_71902,RMVar_hsa_circ_302262,RMVar_hsa_circ_120251,RMVar_hsa_circ_244245,RMVar_hsa_circ_319089,RMVar_hsa_circ_244244,RMVar_hsa_circ_278729,RMVar_hsa_circ_244252,RMVar_hsa_circ_244254,RMVar_hsa_circ_84617,RMVar_hsa_circ_244253,RMVar_hsa_circ_73307 89617 RMVar_ID_89617 Human_SNP_ID_314723316 m1A Human chr7 - 27662805 27662805 27662805 CCCTCCGGGAGGCGGCGGAGGTCACCGCGGGGAGAGGGGCGGGCGCAGCATGGCAGCCTCCTTAC CCCTCCGGGAGGCGGCGGAGGTCACCGCGGGGGGAGGGGCGGGCGCAGCATGGCAGCCTCCTTAC T C HIBADH Ensembl:ENSG00000106049 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr7:27662699..27662875;chr7:27662760..27662931 26863196 MeRIP-seq:(Medium) rs778083226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955699,Human_RBP_ID_5090499,Human_RBP_ID_9337094,Human_RBP_ID_18426515 RMVar_hsa_circ_244254,RMVar_hsa_circ_84617 89618 RMVar_ID_89618 Human_SNP_ID_314723332 m1A Human chr7 - 27662828 27662828 27662828 TGCACACGCTCGCAGTCTGTGGGCCCTCCGGGAGGCGGCGGAGGTCACCGCGGGGAGAGGGGCGG TGCACACGCTCGCAGTCTGTGGGCCCTCCGGGGGGCGGCGGAGGTCACCGCGGGGAGAGGGGCGG T C HIBADH Ensembl:ENSG00000106049 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:27662676..27662968;chr7:27649526..27662883 26863196 MeRIP-seq:(Medium) rs1159211824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955699,Human_RBP_ID_5090499,Human_RBP_ID_9337094,Human_RBP_ID_18426515 RMVar_hsa_circ_244254,RMVar_hsa_circ_84617 89619 RMVar_ID_89619 Human_SNP_ID_314723333 m1A Human chr7 - 27662828 27662828 27662828 TGCACACGCTCGCAGTCTGTGGGCCCTCCGGGAGGCGGCGGAGGTCACCGCGGGGAGAGGGGCGG TGCACACGCTCGCAGTCTGTGGGCCCTCCGGGCGGCGGCGGAGGTCACCGCGGGGAGAGGGGCGG T G HIBADH Ensembl:ENSG00000106049 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:27662676..27662968;chr7:27649526..27662883 26863196 MeRIP-seq:(Medium) rs1159211824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955699,Human_RBP_ID_5090499,Human_RBP_ID_9337094,Human_RBP_ID_18426515 RMVar_hsa_circ_244254,RMVar_hsa_circ_84617 89620 RMVar_ID_89620 Human_SNP_ID_314743659 m1A Human chr7 - 27748466 27748466 27748466 CAAGTTAAATTATACCAACTAAGAATAAACTTATGCCTTCAGAAAATACATAATATTTAATATAA CAAGTTAAATTATACCAACTAAGAATAAACTTGTGCCTTCAGAAAATACATAATATTTAATATAA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:27748455..27748540 26863410 MeRIP-seq:(Medium) rs1301523596 Functional Loss SNV dbSNP153 33..33 33 - - - 89621 RMVar_ID_89621 Human_SNP_ID_314743660 m1A Human chr7 - 27748466 27748466 27748466 CAAGTTAAATTATACCAACTAAGAATAAACTTATGCCTTCAGAAAATACATAATATTTAATATAA CAAGTTAAATTATACCAACTAAGAATAAACTTCTGCCTTCAGAAAATACATAATATTTAATATAA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:27748455..27748540 26863410 MeRIP-seq:(Medium) rs1301523596 Functional Loss SNV dbSNP153 33..33 33 - - - 89622 RMVar_ID_89622 Human_SNP_ID_314752386 m1A Human chr7 + 27785240 27785240 27785240 TTTAAGAAGAGGTTCAGTGATGCTACATCCAAAGCCCATCAGCTTGAGGAAGATATTGTGTCAGT TTTAAGAAGAGGTTCAGTGATGCTACATCCAAGGCCCATCAGCTTGAGGAAGATATTGTGTCAGT A G TAX1BP1 Ensembl:ENSG00000106052 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:27785192..27785292 32194978 MeRIP-seq:(Medium) rs7795659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86831,Human_RBP_ID_682442,Human_RBP_ID_957172,Human_RBP_ID_5219650,Human_RBP_ID_9403271,Human_RBP_ID_17314504,Human_RBP_ID_24549281,Human_RBP_ID_26356373 Human_Splice_Rec_852004,Human_Splice_Rec_852005,Human_Splice_Rec_852042,Human_Splice_Rec_852043,Human_Splice_Rec_852072,Human_Splice_Rec_852073,Human_Splice_Rec_852104,Human_Splice_Rec_852105,Human_Splice_Rec_852136,Human_Splice_Rec_852137,Human_Splice_Rec_852172,Human_Splice_Rec_852173 Human_miRNA_ID_2998267 RMVar_hsa_circ_350845,RMVar_hsa_circ_55973,RMVar_hsa_circ_348816,RMVar_hsa_circ_244255,RMVar_hsa_circ_343217,RMVar_hsa_circ_67299,RMVar_hsa_circ_43694,RMVar_hsa_circ_361313,RMVar_hsa_circ_369213,RMVar_hsa_circ_363035,RMVar_hsa_circ_365518,RMVar_hsa_circ_7569,RMVar_hsa_circ_368257,RMVar_hsa_circ_359962,RMVar_hsa_circ_99238,RMVar_hsa_circ_287900,RMVar_hsa_circ_325686,RMVar_hsa_circ_282539,RMVar_hsa_circ_244261,RMVar_hsa_circ_244262,RMVar_hsa_circ_244263,RMVar_hsa_circ_244260 89623 RMVar_ID_89623 Human_SNP_ID_314765065 m1A Human chr7 - 27837594 27837594 27837594 AGACTTACTCCCCTCTCCGCCCCTCATAGGTCAAGTTCTCATCCTCCCCACATGCTCTTTCTACA AGACTTACTCCCCTCTCCGCCCCTCATAGGTCGAGTTCTCATCCTCCCCACATGCTCTTTCTACA T C JAZF1 Ensembl:ENSG00000153814 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:27837573..27837657 26863196 MeRIP-seq:(Medium) rs1423148048 Functional Loss SNV dbSNP153 33..33 33 - - - 89624 RMVar_ID_89624 Human_SNP_ID_314783176 m1A Human chr7 + 27908065 27908065 27908065 ACTTTATCCCTTCTCAGAAAATCAGAGAACAAAGCTGGCAGACTGTAATATCTGAGAGAGAAAGT ACTTTATCCCTTCTCAGAAAATCAGAGAACAAGGCTGGCAGACTGTAATATCTGAGAGAGAAAGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:27908050..27908177 26863196 MeRIP-seq:(Medium) rs753725576 Functional Loss SNV dbSNP153 33..33 33 - - - 89625 RMVar_ID_89625 Human_SNP_ID_314829302 m1A Human chr7 + 28103680 28103680 28103680 TTGGTTTCTTTCTTTCTCTCATACCTAAACCAAACCTGTTGACCTTATCTCTAAAATCTACCCAG TTGGTTTCTTTCTTTCTCTCATACCTAAACCACACCTGTTGACCTTATCTCTAAAATCTACCCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:28103669..28103779 26863196 MeRIP-seq:(Medium) rs1048527372 Functional Loss SNV dbSNP153 33..33 33 - - - 89626 RMVar_ID_89626 Human_SNP_ID_314829303 m1A Human chr7 + 28103680 28103680 28103680 TTGGTTTCTTTCTTTCTCTCATACCTAAACCAAACCTGTTGACCTTATCTCTAAAATCTACCCAG TTGGTTTCTTTCTTTCTCTCATACCTAAACCAGACCTGTTGACCTTATCTCTAAAATCTACCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:28103669..28103779 26863196 MeRIP-seq:(Medium) rs1048527372 Functional Loss SNV dbSNP153 33..33 33 - - - 89627 RMVar_ID_89627 Human_SNP_ID_314847380 m1A Human chr7 - 28179235 28179235 28179235 TCCAACCACCTGCGGAAGGTGTGACCGACGCCAGCGAGTTGTCCTGCGTGGGCTAGAAGGTGAAG TCCAACCACCTGCGGAAGGTGTGACCGACGCCTGCGAGTTGTCCTGCGTGGGCTAGAAGGTGAAG T A JAZF1 Ensembl:ENSG00000153814 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:28179233..28179403 26863196 MeRIP-seq:(Medium) rs757154387 Functional Loss SNV dbSNP153 33..33 33 - - - 89628 RMVar_ID_89628 Human_SNP_ID_314847887 m1A Human chr7 - 28180587 28180587 28180587 CGCTCGCAGAGCCGACACCAGGGGGGCTCTCGATGTAGCACCATGACAGGCATCGCCGCCGCCTC CGCTCGCAGAGCCGACACCAGGGGGGCTCTCGCTGTAGCACCATGACAGGCATCGCCGCCGCCTC T G JAZF1 Ensembl:ENSG00000153814 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:28180440..28180804 26863196 MeRIP-seq:(Medium) rs369574145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18881419 89629 RMVar_ID_89629 Human_SNP_ID_315206725 m1A Human chr7 + 29646802 29646802 29646802 CTTTCTTTTTTCTTTGCCTCACCTCCTCTCCCACATCTCTATTCCTCCCAGCCTTTCTTCACTCC CTTTCTTTTTTCTTTGCCTCACCTCCTCTCCCGCATCTCTATTCCTCCCAGCCTTTCTTCACTCC A G lnc-WIPF3-2 RNACentral:URS00008B8D43 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:29646751..29646836;chr7:29646640..29646876 26863196 MeRIP-seq:(Medium) rs200864819 Functional Loss SNV dbSNP153 33..33 33 - - - 89630 RMVar_ID_89630 Human_SNP_ID_315206726 m1A Human chr7 + 29646802 29646802 29646802 CTTTCTTTTTTCTTTGCCTCACCTCCTCTCCCACATCTCTATTCCTCCCAGCCTTTCTTCACTCC CTTTCTTTTTTCTTTGCCTCACCTCCTCTCCCTCATCTCTATTCCTCCCAGCCTTTCTTCACTCC A T lnc-WIPF3-2 RNACentral:URS00008B8D43 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:29646751..29646836;chr7:29646640..29646876 26863196 MeRIP-seq:(Medium) rs200864819 Functional Loss SNV dbSNP153 33..33 33 - - - 89631 RMVar_ID_89631 Human_SNP_ID_315207372 m1A Human chr7 - 29649368 29649368 29649368 ACAGCTCCATGTACAGCCCCTCATACGTTCACAGCCCCAGTGGCGCAGAACCCATCACTACTCGC ACAGCTCCATGTACAGCCCCTCATACGTTCACGGCCCCAGTGGCGCAGAACCCATCACTACTCGC T C ZNRF2P2 Ensembl:ENSG00000225264 Pseudogene intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:29649284..29649486 26863196 MeRIP-seq:(Medium) rs1452045172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17543603,Human_RBP_ID_21904420 89632 RMVar_ID_89632 Human_SNP_ID_315207872 m1A Human chr7 - 29650821 29650821 29650821 GCAGGTTCCCTCCGCCTAGGGTCGAAAGCTTCAGAGGCAGCCCCAACTCTTCCACTTCTTCCTCC GCAGGTTCCCTCCGCCTAGGGTCGAAAGCTTCGGAGGCAGCCCCAACTCTTCCACTTCTTCCTCC T C ZNRF2P2 Ensembl:ENSG00000225264 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:29650784..29650884 26863196 MeRIP-seq:(Medium) rs1308187613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273089 89633 RMVar_ID_89633 Human_SNP_ID_315215978 m1A Human chr7 - 29685573 29685573 29685573 TAGCAGCGGCCGCCGGAGACTAGGCGGTGCGGAGGCCCGGGGCGCCAAGCGCGGCGGCAGAAAGC TAGCAGCGGCCGCCGGAGACTAGGCGGTGCGGTGGCCCGGGGCGCCAAGCGCGGCGGCAGAAAGC T A LOC646762,LOC646762:2 RNACentral:URS0000D5D10C,RNACentral:URS00008C28D9 lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:29685426..29685621 26863196 MeRIP-seq:(Medium) rs562082367 Functional Loss SNV dbSNP153 33..33 33 - - - 89634 RMVar_ID_89634 Human_SNP_ID_315215979 m1A Human chr7 - 29685573 29685573 29685573 TAGCAGCGGCCGCCGGAGACTAGGCGGTGCGGAGGCCCGGGGCGCCAAGCGCGGCGGCAGAAAGC TAGCAGCGGCCGCCGGAGACTAGGCGGTGCGGGGGCCCGGGGCGCCAAGCGCGGCGGCAGAAAGC T C LOC646762,LOC646762:2 RNACentral:URS0000D5D10C,RNACentral:URS00008C28D9 lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:29685426..29685621 26863196 MeRIP-seq:(Medium) rs562082367 Functional Loss SNV dbSNP153 33..33 33 - - - 89635 RMVar_ID_89635 Human_SNP_ID_315215986 m1A Human chr7 - 29685589 29685589 29685589 CGGAGGATGGCGGCGGTAGCAGCGGCCGCCGGAGACTAGGCGGTGCGGAGGCCCGGGGCGCCAAG CGGAGGATGGCGGCGGTAGCAGCGGCCGCCGGGGACTAGGCGGTGCGGAGGCCCGGGGCGCCAAG T C LOC646762,LOC646762:2 RNACentral:URS0000D5D10C,RNACentral:URS00008C28D9 lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:29685411..29685629 26863196 MeRIP-seq:(Medium) rs1353766685 Functional Loss SNV dbSNP153 33..33 33 - - - 89636 RMVar_ID_89636 Human_SNP_ID_315260686 m1A Human chr7 - 29884169 29884169 29884169 GGGGGTGGCGTTGGGGGAGGTGGCGGAGGTGGAGGTGGTGGCGCACAGGGGACGGGGGGTGCAAC GGGGGTGGCGTTGGGGGAGGTGGCGGAGGTGGGGGTGGTGGCGCACAGGGGACGGGGGGTGCAAC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:29884119..29884232 26863196 MeRIP-seq:(Medium) rs1288660689 Functional Loss SNV dbSNP153 33..33 33 - - - 89637 RMVar_ID_89637 Human_SNP_ID_315269719 m1A Human chr7 - 29920529 29920529 29920529 CCCTTGCTGGGCATGCTTCGTAGAGGGCCAGGAGCAGCAGGTCATGTGCACATGCCGTTGCAGCA CCCTTGCTGGGCATGCTTCGTAGAGGGCCAGGGGCAGCAGGTCATGTGCACATGCCGTTGCAGCA T C SCRN1 Ensembl:ENSG00000136193 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:29920479..29920644 26863196 MeRIP-seq:(Medium) rs1228083443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682733,Human_RBP_ID_7731176,Human_RBP_ID_9354823 Human_miRNA_ID_255647 89638 RMVar_ID_89638 Human_SNP_ID_315269727 m1A Human chr7 - 29920549 29920549 29920549 GAGGAGGGACGGAGGAGGTTCCCTTGCTGGGCATGCTTCGTAGAGGGCCAGGAGCAGCAGGTCAT GAGGAGGGACGGAGGAGGTTCCCTTGCTGGGCGTGCTTCGTAGAGGGCCAGGAGCAGCAGGTCAT T C SCRN1 Ensembl:ENSG00000136193 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:29920501..29920575 32194978 MeRIP-seq:(Medium) rs1411765064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3843594,Human_RBP_ID_7731176,Human_RBP_ID_9354823 89639 RMVar_ID_89639 Human_SNP_ID_315275462 m1A Human chr7 - 29944181 29944181 29944181 TGACTGAAGTATGGTTCTGGTTTCCTTCCTGCAGGCTTGGTTTAGAAAGAGGGGAAACAGCTAAA TGACTGAAGTATGGTTCTGGTTTCCTTCCTGCGGGCTTGGTTTAGAAAGAGGGGAAACAGCTAAA T C SCRN1 Ensembl:ENSG00000136193 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:29944151..29944200 32194978 MeRIP-seq:(Medium) rs753889874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26098799 RMVar_hsa_circ_244304,RMVar_hsa_circ_244305,RMVar_hsa_circ_342501,RMVar_hsa_circ_244307,RMVar_hsa_circ_318752,RMVar_hsa_circ_295319,RMVar_hsa_circ_244308,RMVar_hsa_circ_244309,RMVar_hsa_circ_329641,RMVar_hsa_circ_279626,RMVar_hsa_circ_244310,RMVar_hsa_circ_34097,RMVar_hsa_circ_375762,RMVar_hsa_circ_244312 89640 RMVar_ID_89640 Human_SNP_ID_698925649 m1A Human chr22 + 20016383 20016383 20016383 CGCCCCCGCCGGCCCGGGGTCTCGGACGCCGCAGAGCGCGCGGACAAGACGCGGGTGGGGCGGAG CGCCCCCGCCGGCCCGGGGTCTCGGACGCCGCCGAGCGCGCGGACAAGACGCGGGTGGGGCGGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20016380..20016463 26863196 MeRIP-seq:(Medium) rs559562519 Functional Loss SNV dbSNP153 33..33 33 - - - 89641 RMVar_ID_89641 Human_SNP_ID_698925650 m1A Human chr22 + 20016383 20016383 20016383 CGCCCCCGCCGGCCCGGGGTCTCGGACGCCGCAGAGCGCGCGGACAAGACGCGGGTGGGGCGGAG CGCCCCCGCCGGCCCGGGGTCTCGGACGCCGCGGAGCGCGCGGACAAGACGCGGGTGGGGCGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20016380..20016463 26863196 MeRIP-seq:(Medium) rs559562519 Functional Loss SNV dbSNP153 33..33 33 - - - 89642 RMVar_ID_89642 Human_SNP_ID_698925658 m1A Human chr22 - 20016418 20016418 20016418 CCGGGCGAGGGTCTGGGCCGGACGTCGGAGCCAATCTCCGCCCCACCCGCGTCTTGTCCGCGCGC CCGGGCGAGGGTCTGGGCCGGACGTCGGAGCCGATCTCCGCCCCACCCGCGTCTTGTCCGCGCGC T C ARVCF Ensembl:ENSG00000099889 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20016395..20016557 26863196 MeRIP-seq:(Medium) rs1047589232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676611,Human_RBP_ID_18497175,Human_RBP_ID_22602987 89643 RMVar_ID_89643 Human_SNP_ID_698925659 m1A Human chr22 - 20016418 20016418 20016418 CCGGGCGAGGGTCTGGGCCGGACGTCGGAGCCAATCTCCGCCCCACCCGCGTCTTGTCCGCGCGC CCGGGCGAGGGTCTGGGCCGGACGTCGGAGCCCATCTCCGCCCCACCCGCGTCTTGTCCGCGCGC T G ARVCF Ensembl:ENSG00000099889 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20016395..20016557 26863196 MeRIP-seq:(Medium) rs1047589232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676611,Human_RBP_ID_18497175,Human_RBP_ID_22602987 89644 RMVar_ID_89644 Human_SNP_ID_698927035 m1A Human chr22 - 20021148 20021148 20021148 GCCGGGCCACTAGCGGAGTCGGCCAGCCCCGGAGCCGCGCACTCACCGCCTCCGCCACCGCCGCC GCCGGGCCACTAGCGGAGTCGGCCAGCCCCGGGGCCGCGCACTCACCGCCTCCGCCACCGCCGCC T C lnc-ARVCF-1,lnc-ARVCF-1:2,lnc-ARVCF-1:3,lnc-ARVCF-1:4,lnc-ARVCF-1:5,lnc-ARVCF-1:6 RNACentral:URS00008BBC72,RNACentral:URS00008B344C,RNACentral:URS00008B7E1E,RNACentral:URS00008BF769,RNACentral:URS00008B775A,RNACentral:URS00008BF6AA lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:20021142..20021291;chr22:20021130..20021307 26863196 MeRIP-seq:(Medium) rs1431434651 Functional Loss SNV dbSNP153 33..33 33 - - - 89645 RMVar_ID_89645 Human_SNP_ID_698931182 m1A Human chr22 + 20037080 20037080 20037080 GTCAATGTACAAAGACGTGAAGACTCAGCCACAGAAGGCAGCCACAGGTAGGACAGAGGAGTGAC GTCAATGTACAAAGACGTGAAGACTCAGCCACGGAAGGCAGCCACAGGTAGGACAGAGGAGTGAC A G TANGO2 Ensembl:ENSG00000183597 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20037074..20037238 26863196 MeRIP-seq:(Medium) rs1366821369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21896463 Human_Splice_Rec_2138591,Human_Splice_Rec_2138643,Human_Splice_Rec_2138667,Human_Splice_Rec_2138747 RMVar_hsa_circ_40633,RMVar_hsa_circ_78613,RMVar_hsa_circ_322200,RMVar_hsa_circ_212986,RMVar_hsa_circ_333417,RMVar_hsa_circ_120947,RMVar_hsa_circ_212987,RMVar_hsa_circ_10880,RMVar_hsa_circ_212988 89646 RMVar_ID_89646 Human_SNP_ID_698932845 m1A Human chr22 - 20043442 20043439 20043442 CAGCCACCGCTGAGCACGCAGGAAGACTCACCACTGAGGATCTCGTTGTTGTTCCCCCAGAAGTC CAGCCACCGCTGAGCACGCAGGAAGACTCACC___GAGGATCTCGTTGTTGTTCCCCCAGAAGTC CAGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:20043397..20043529 26863196 MeRIP-seq:(Medium) rs1036098015 Functional Loss DEL dbSNP153 33..35 33 - - - 89647 RMVar_ID_89647 Human_SNP_ID_698943037 m1A Human chr22 - 20080360 20080360 20080360 CGCACCTACCTGAGGCGCCCGCGGGCTGCCCAAGCCGCCCGCAGCCAAACCACAGCCGGGAAAGC CGCACCTACCTGAGGCGCCCGCGGGCTGCCCAGGCCGCCCGCAGCCAAACCACAGCCGGGAAAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:20080324..20080488 26863196 MeRIP-seq:(Medium) rs1256598066 Functional Loss SNV dbSNP153 33..33 33 - - - 89648 RMVar_ID_89648 Human_SNP_ID_698943515 m1A Human chr22 + 20081798 20081798 20081798 AGTAGCCATATCCAAACCAAACTCAAATCTTCACCCATGCCAAAACATTCCTTGGCCTATCTAAA AGTAGCCATATCCAAACCAAACTCAAATCTTCCCCCATGCCAAAACATTCCTTGGCCTATCTAAA A C DGCR8 Ensembl:ENSG00000128191 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20081794..20081941 26863196 MeRIP-seq:(Medium) rs956664820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8262265,Human_RBP_ID_9124514,Human_RBP_ID_17087602,Human_RBP_ID_17285029,Human_RBP_ID_17398347,Human_RBP_ID_17982329,Human_RBP_ID_20724120 89649 RMVar_ID_89649 Human_SNP_ID_698945838 m1A Human chr22 + 20090104 20090104 20090104 GGGGATGTGTCCCCCGTCAAGCCCCTGAGCCGATCTGCAGAGCTGGAGTTTCCCCTGGATGAGCC GGGGATGTGTCCCCCGTCAAGCCCCTGAGCCGCTCTGCAGAGCTGGAGTTTCCCCTGGATGAGCC A C DGCR8 Ensembl:ENSG00000128191 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20090053..20090153 32194978 MeRIP-seq:(Medium) rs1312422281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1939834,Human_RBP_ID_4685895,Human_RBP_ID_5202899,Human_RBP_ID_7062893,Human_RBP_ID_8861347,Human_RBP_ID_9391961,Human_RBP_ID_14398871,Human_RBP_ID_17982337,Human_RBP_ID_18784648,Human_RBP_ID_19008527,Human_RBP_ID_22479730,Human_RBP_ID_23015350,Human_RBP_ID_26344873,Human_RBP_ID_27565109,Human_RBP_ID_27821078 Human_miRNA_ID_2396410 RMVar_hsa_circ_8716,RMVar_hsa_circ_110770,RMVar_hsa_circ_347926,RMVar_hsa_circ_355371,RMVar_hsa_circ_212994,RMVar_hsa_circ_320308,RMVar_hsa_circ_212995 89650 RMVar_ID_89650 Human_SNP_ID_698950318 m1A Human chr22 + 20107394 20107394 20107394 CATGTATGGCCGTGAGAGCAGCAAGATGGTCAAGCAGGTAACTGGCCATCAGCAGGTCCCAGGGC CATGTATGGCCGTGAGAGCAGCAAGATGGTCAGGCAGGTAACTGGCCATCAGCAGGTCCCAGGGC A G DGCR8 Ensembl:ENSG00000128191 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20107301..20107455 26863196 MeRIP-seq:(Medium) rs1450137492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10569,Human_RBP_ID_929217,Human_RBP_ID_3962036,Human_RBP_ID_22673988,Human_RBP_ID_26345088 Human_Splice_Rec_2138895,Human_Splice_Rec_2138921,Human_Splice_Rec_2138945,Human_Splice_Rec_2138967,Human_Splice_Rec_2138987,Human_Splice_Rec_2139001 RMVar_hsa_circ_8716,RMVar_hsa_circ_29796,RMVar_hsa_circ_91221,RMVar_hsa_circ_212999,RMVar_hsa_circ_359001,RMVar_hsa_circ_213001 89651 RMVar_ID_89651 Human_SNP_ID_698950720 m1A Human chr22 - 20108896 20108895 20108896 ATACTGCTGCAGCTCAATCACACTCTTGTCCGATGTCTCCTGGGAAGTATAGCACCTCACGCTCA ATACTGCTGCAGCTCAATCACACTCTTGTCCG_TGTCTCCTGGGAAGTATAGCACCTCACGCTCA AT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20108847..20108997 32194978 MeRIP-seq:(Medium) rs1568963433 Functional Loss DEL dbSNP153 33..33 33 - - - 89652 RMVar_ID_89652 Human_SNP_ID_698950993 m1A Human chr22 + 20109988 20109988 20109988 ACCTTGTGTCTTCCCGAGCCTCTGCCAAGCCCACCTCACTGGTACCCCTGACCTTTGTTGTTCTT ACCTTGTGTCTTCCCGAGCCTCTGCCAAGCCCGCCTCACTGGTACCCCTGACCTTTGTTGTTCTT A G DGCR8 Ensembl:ENSG00000128191 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:20109979..20110200 26863196 MeRIP-seq:(Medium) rs777252490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22673991,Human_RBP_ID_22744290 89653 RMVar_ID_89653 Human_SNP_ID_698951050 m1A Human chr22 + 20110126 20110114 20110126 ACCGTGGACGTGTGAGGGAGGTGGCACGGGCCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGG ACCGTGGACGTGTGAGGGAGG____________GGGCGCGGGGGCCGCCAGCCGCACTTCTGAGG GTGGCACGGGCCA G DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20110006..20110225 26863196 MeRIP-seq:(Medium) rs1242417957 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_23115704 Human_miRNA_ID_111468,Human_miRNA_ID_940442 89654 RMVar_ID_89654 Human_SNP_ID_698951054 m1A Human chr22 + 20110126 20110126 20110126 ACCGTGGACGTGTGAGGGAGGTGGCACGGGCCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGG ACCGTGGACGTGTGAGGGAGGTGGCACGGGCCGGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGG A G DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20110006..20110225 26863196 MeRIP-seq:(Medium) rs973816910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23115704 Human_miRNA_ID_111468,Human_miRNA_ID_940442 89655 RMVar_ID_89655 Human_SNP_ID_698951068 m1A Human chr22 + 20110143 20110143 20110143 GAGGTGGCACGGGCCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGGAGACCAGCAGTCATGCA GAGGTGGCACGGGCCAGGGCGCGGGGGCCGCCCGCCGCACTTCTGAGGAGACCAGCAGTCATGCA A C DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:20110031..20110175 26863196 MeRIP-seq:(Medium) rs1198127750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575552,Human_RBP_ID_22819560,Human_RBP_ID_23115704 89656 RMVar_ID_89656 Human_SNP_ID_698951075 m1A Human chr22 - 20110151 20110151 20110151 GTGCACGATGCATGACTGCTGGTCTCCTCAGAAGTGCGGCTGGCGGCCCCCGCGCCCTGGCCCGT GTGCACGATGCATGACTGCTGGTCTCCTCAGACGTGCGGCTGGCGGCCCCCGCGCCCTGGCCCGT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:20110026..20110200 26863196 MeRIP-seq:(Medium) rs764009270 Functional Loss SNV dbSNP153 33..33 33 - - - 89657 RMVar_ID_89657 Human_SNP_ID_698951076 m1A Human chr22 + 20110156 20110154 20110157 CCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGGAGACCAGCAGTCATGCATCGTGCACCACAG CCAGGGCGCGGGGGCCGCCAGCCGCACTTCT___GAGACCAGCAGTCATGCATCGTGCACCACAG TGAG T DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20110002..20110225 26863196 MeRIP-seq:(Medium) rs756228599 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_575552,Human_RBP_ID_22819560,Human_RBP_ID_23115704 89658 RMVar_ID_89658 Human_SNP_ID_698951077 m1A Human chr22 + 20110156 20110156 20110156 CCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGAGGAGACCAGCAGTCATGCATCGTGCACCACAG CCAGGGCGCGGGGGCCGCCAGCCGCACTTCTGTGGAGACCAGCAGTCATGCATCGTGCACCACAG A T DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20110002..20110225 26863196 MeRIP-seq:(Medium) rs1284234133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575552,Human_RBP_ID_22819560,Human_RBP_ID_23115704 89659 RMVar_ID_89659 Human_SNP_ID_698951536 m1A Human chr22 + 20111599 20111599 20111599 GCCCTTAGCCAGCCAGATGCGCCTGTGAACCAAAGCTTCGTGCACATGTGTTCCCCTAAAGGTTG GCCCTTAGCCAGCCAGATGCGCCTGTGAACCACAGCTTCGTGCACATGTGTTCCCCTAAAGGTTG A C DGCR8 Ensembl:ENSG00000128191 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:20111551..20111793 26863196 MeRIP-seq:(Medium) rs1197114442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575570,Human_RBP_ID_1028398,Human_RBP_ID_1608203,Human_RBP_ID_9124528,Human_RBP_ID_14399665 89660 RMVar_ID_89660 Human_SNP_ID_698952219 m1A Human chr22 + 20113006 20113006 20113006 TTAGCTCTCCGGATGGCCAGGATCACCTTGGAATCTGAGGAGGCAAACACCAGCTGGGTCCCCAC TTAGCTCTCCGGATGGCCAGGATCACCTTGGACTCTGAGGAGGCAAACACCAGCTGGGTCCCCAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20112905..20113055 32194978 MeRIP-seq:(Medium) rs764259215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1608216,Human_RBP_ID_8545985,Human_RBP_ID_14399722,Human_RBP_ID_18784743 89661 RMVar_ID_89661 Human_SNP_ID_698953279 m1A Human chr22 - 20115392 20115392 20115392 GTTTCTGGTTGGCGTCGGGGTGGATGGGGAGGATAACACCGTGGGCTGTCGGCTCGGCAAGTACA GTTTCTGGTTGGCGTCGGGGTGGATGGGGAGGGTAACACCGTGGGCTGTCGGCTCGGCAAGTACA T C TRMT2A Ensembl:ENSG00000099899 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20115343..20115445 26863196 MeRIP-seq:(Medium) rs759610393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780970,Human_RBP_ID_833305,Human_RBP_ID_929227,Human_RBP_ID_3962046,Human_RBP_ID_5387223,Human_RBP_ID_8865551,Human_RBP_ID_9300218,Human_RBP_ID_17982368,Human_RBP_ID_19007638,Human_RBP_ID_22426520,Human_RBP_ID_23010887,Human_RBP_ID_23935885,Human_RBP_ID_26770937,Human_RBP_ID_27032088 Human_Splice_Rec_2139010,Human_Splice_Rec_2139034,Human_Splice_Rec_2139064,Human_Splice_Rec_2139092,Human_Splice_Rec_2139118,Human_Splice_Rec_2139134 RMVar_hsa_circ_104094,RMVar_hsa_circ_213003,RMVar_hsa_circ_114685,RMVar_hsa_circ_213007,RMVar_hsa_circ_65491,RMVar_hsa_circ_86327,RMVar_hsa_circ_213010 89662 RMVar_ID_89662 Human_SNP_ID_698953812 m1A Human chr22 - 20116526 20116526 20116526 CCTACCGTCTCGGTGCCCCCTGCAGCCCCGGCAGCCCTGGAGGAGGTGGAGAAAGAGGGCGCTGG CCTACCGTCTCGGTGCCCCCTGCAGCCCCGGCGGCCCTGGAGGAGGTGGAGAAAGAGGGCGCTGG T C TRMT2A Ensembl:ENSG00000099899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20116476..20117205 26863196 MeRIP-seq:(Medium) rs1370436431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4686037,Human_RBP_ID_5204542,Human_RBP_ID_8865852 Human_Splice_Rec_2139006,Human_Splice_Rec_2139030,Human_Splice_Rec_2139060,Human_Splice_Rec_2139088,Human_Splice_Rec_2139176,Human_Splice_Rec_2139182,Human_Splice_Rec_2139186 RMVar_hsa_circ_104094,RMVar_hsa_circ_213003,RMVar_hsa_circ_86327,RMVar_hsa_circ_213010 89663 RMVar_ID_89663 Human_SNP_ID_698953813 m1A Human chr22 - 20116526 20116526 20116526 CCTACCGTCTCGGTGCCCCCTGCAGCCCCGGCAGCCCTGGAGGAGGTGGAGAAAGAGGGCGCTGG CCTACCGTCTCGGTGCCCCCTGCAGCCCCGGCCGCCCTGGAGGAGGTGGAGAAAGAGGGCGCTGG T G TRMT2A Ensembl:ENSG00000099899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20116476..20117205 26863196 MeRIP-seq:(Medium) rs1370436431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4686037,Human_RBP_ID_5204542,Human_RBP_ID_8865852 Human_Splice_Rec_2139006,Human_Splice_Rec_2139030,Human_Splice_Rec_2139060,Human_Splice_Rec_2139088,Human_Splice_Rec_2139176,Human_Splice_Rec_2139182,Human_Splice_Rec_2139186 RMVar_hsa_circ_104094,RMVar_hsa_circ_213003,RMVar_hsa_circ_86327,RMVar_hsa_circ_213010 89664 RMVar_ID_89664 Human_SNP_ID_698953832 m1A Human chr22 + 20116551 20116551 20116551 CCAGGGCTGCCGGGGCTGCAGGGGGCACCGAGACGGTAGGGCAGCTCAGGGCACTGCTGCTCTCC CCAGGGCTGCCGGGGCTGCAGGGGGCACCGAGGCGGTAGGGCAGCTCAGGGCACTGCTGCTCTCC A G RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20116501..20116625 26863196 MeRIP-seq:(Medium) rs752184626 Functional Loss SNV dbSNP153 33..33 33 - - - 89665 RMVar_ID_89665 Human_SNP_ID_698954233 m1A Human chr22 - 20117576 20117549 20117577 GCTGGCTCCGCGGCCTCTCGGCGGCTACTCGTAGCTCCTTCCCTCCGCGTCTGGCGCCGGCGCCT GCTGGCTCCGCGGCCTCTCGGCGGCTACTCG____________________________GCGCCT CCGGCGCCAGACGCGGAGGGAAGGAGCTA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr22:20117445..20117977;chr22:20117411..20118042;chr22:20117551..20117575 26863196 MeRIP-seq:(Medium) rs1469796776 Functional Loss DEL dbSNP153 32..59 33 - - - 89666 RMVar_ID_89666 Human_SNP_ID_698954267 m1A Human chr22 + 20117621 20117621 20117621 CGAGAGGCCGCGGAGCCAGCGACGACCGACCCAGCCGAGCCGCCGCCGCCGCCGCGCCCCCATGG CGAGAGGCCGCGGAGCCAGCGACGACCGACCCTGCCGAGCCGCCGCCGCCGCCGCGCCCCCATGG A T RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr22:20117527..20117674;chr22:20117525..20117675 26863196,26863410 MeRIP-seq:(Medium) rs913259257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4686082,Human_RBP_ID_5388833,Human_RBP_ID_5473409,Human_RBP_ID_8235672,Human_RBP_ID_8943149,Human_RBP_ID_9391969,Human_RBP_ID_9434110,Human_RBP_ID_18168824,Human_RBP_ID_26344875,Human_RBP_ID_27032116 Human_Splice_Rec_2139209,Human_Splice_Rec_2139219,Human_Splice_Rec_2139223,Human_Splice_Rec_2139233,Human_Splice_Rec_2139239 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012 89667 RMVar_ID_89667 Human_SNP_ID_698954443 m1A Human chr22 + 20118088 20118088 20118088 TCATTCATTCGGTTCTTACGTCTGGAACCGCCACTGGCCTCTGTGGCAGAAGCTCGCGTTCCAGC TCATTCATTCGGTTCTTACGTCTGGAACCGCCCCTGGCCTCTGTGGCAGAAGCTCGCGTTCCAGC A C RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20118081..20118241 26863196 MeRIP-seq:(Medium) rs921958601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1608238,Human_RBP_ID_4709991,Human_RBP_ID_8861422,Human_RBP_ID_14399761,Human_RBP_ID_18497289 Human_Splice_Rec_2139241 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012 89668 RMVar_ID_89668 Human_SNP_ID_698954444 m1A Human chr22 + 20118088 20118088 20118088 TCATTCATTCGGTTCTTACGTCTGGAACCGCCACTGGCCTCTGTGGCAGAAGCTCGCGTTCCAGC TCATTCATTCGGTTCTTACGTCTGGAACCGCCGCTGGCCTCTGTGGCAGAAGCTCGCGTTCCAGC A G RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20118081..20118241 26863196 MeRIP-seq:(Medium) rs921958601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1608238,Human_RBP_ID_4709991,Human_RBP_ID_8861422,Human_RBP_ID_14399761,Human_RBP_ID_18497289 Human_Splice_Rec_2139241 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012 89669 RMVar_ID_89669 Human_SNP_ID_698954446 m1A Human chr22 - 20118090 20118090 20118090 ACGCTGGAACGCGAGCTTCTGCCACAGAGGCCAGTGGCGGTTCCAGACGTAAGAACCGAATGAAT ACGCTGGAACGCGAGCTTCTGCCACAGAGGCCGGTGGCGGTTCCAGACGTAAGAACCGAATGAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20118088..20118173 26863196 MeRIP-seq:(Medium) rs181848397 Functional Loss SNV dbSNP153 33..33 33 - - - 89670 RMVar_ID_89670 Human_SNP_ID_698954715 m1A Human chr22 + 20119003 20119003 20119003 AGATCCATAGGCCAGCAGTGTAACCTCTTTGTATCTCCACAGGACACTCATGAGGACCATGATAC AGATCCATAGGCCAGCAGTGTAACCTCTTTGTGTCTCCACAGGACACTCATGAGGACCATGATAC A G RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20119001..20119100 26863196 MeRIP-seq:(Medium) rs747883517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22674002,Human_RBP_ID_22744294,Human_RBP_ID_25655652 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012 89671 RMVar_ID_89671 Human_SNP_ID_698954716 m1A Human chr22 + 20119003 20119003 20119003 AGATCCATAGGCCAGCAGTGTAACCTCTTTGTATCTCCACAGGACACTCATGAGGACCATGATAC AGATCCATAGGCCAGCAGTGTAACCTCTTTGTTTCTCCACAGGACACTCATGAGGACCATGATAC A T RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20119001..20119100 26863196 MeRIP-seq:(Medium) rs747883517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22674002,Human_RBP_ID_22744294,Human_RBP_ID_25655652 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012 89672 RMVar_ID_89672 Human_SNP_ID_698956072 m1A Human chr22 - 20123038 20123038 20123038 CCCAGACACCAGACCCCCAACCACACACCCCCAACCACCCCCGCCAGACACCACACCCAACCACA CCCAGACACCAGACCCCCAACCACACACCCCCCACCACCCCCGCCAGACACCACACCCAACCACA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20123035..20123295 26863196 MeRIP-seq:(Medium) rs960790115 Functional Loss SNV dbSNP153 33..33 33 - - - 89673 RMVar_ID_89673 Human_SNP_ID_698956275 m1A Human chr22 - 20123476 20123476 20123476 CTCTCTCACACACACCCCCACCGCGATACCGCACCCCCTCAGACACCAAACCCCCCCAGACACCA CTCTCTCACACACACCCCCACCGCGATACCGCCCCCCCTCAGACACCAAACCCCCCCAGACACCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:20123473..20123693;chr22:20123473..20123680 26863196 MeRIP-seq:(Medium) rs912707833 Functional Loss SNV dbSNP153 33..33 33 - - - 89674 RMVar_ID_89674 Human_SNP_ID_698956284 m1A Human chr22 + 20123503 20123501 20123503 GGGGGTGCGGTATCGCGGTGGGGGTGTGTGTGAGAGAGATTGGGGGTGTTCGGGCAGTGTAAGAG GGGGGTGCGGTATCGCGGTGGGGGTGTGTGT__GAGAGATTGGGGGTGTTCGGGCAGTGTAAGAG TGA T RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20123500..20123585 26863196 MeRIP-seq:(Medium) rs1350072488 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10241,Human_RBP_ID_210913,Human_RBP_ID_265355,Human_RBP_ID_575602,Human_RBP_ID_3675906,Human_RBP_ID_5148930,Human_RBP_ID_5240766,Human_RBP_ID_5324043,Human_RBP_ID_5387631,Human_RBP_ID_5653370,Human_RBP_ID_8117948,Human_RBP_ID_8207152,Human_RBP_ID_8235482,Human_RBP_ID_8943260,Human_RBP_ID_9332633,Human_RBP_ID_9341291,Human_RBP_ID_9432814,Human_RBP_ID_17193657,Human_RBP_ID_17286612,Human_RBP_ID_18413075,Human_RBP_ID_18497295,Human_RBP_ID_18952367,Human_RBP_ID_19111606,Human_RBP_ID_21985012,Human_RBP_ID_22371611,Human_RBP_ID_22479954,Human_RBP_ID_22525768,Human_RBP_ID_22604162,Human_RBP_ID_22723905,Human_RBP_ID_23285878,Human_RBP_ID_23935938,Human_RBP_ID_24553844,Human_RBP_ID_26770940,Human_RBP_ID_26789478,Human_RBP_ID_27841060 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_81712,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012,RMVar_hsa_circ_335831,RMVar_hsa_circ_213013 89675 RMVar_ID_89675 Human_SNP_ID_698956398 m1A Human chr22 + 20123924 20123924 20123924 TGCGTGTCCGGCGGGGCAGGGTCCCTCATCCCAGGTGCAGGATGACTGCTGGCAGGAGCCTGAGT TGCGTGTCCGGCGGGGCAGGGTCCCTCATCCCGGGTGCAGGATGACTGCTGGCAGGAGCCTGAGT A G RANBP1 Ensembl:ENSG00000099901 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20123921..20124080 26863196 MeRIP-seq:(Medium) rs939319449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3675915,Human_RBP_ID_5149156,Human_RBP_ID_5204220,Human_RBP_ID_5240769,Human_RBP_ID_5324044,Human_RBP_ID_5653376,Human_RBP_ID_8117954,Human_RBP_ID_8207154,Human_RBP_ID_8235736,Human_RBP_ID_9333225,Human_RBP_ID_9433094,Human_RBP_ID_17146882,Human_RBP_ID_18168543,Human_RBP_ID_18423693,Human_RBP_ID_18497299,Human_RBP_ID_18952370,Human_RBP_ID_21985730,Human_RBP_ID_22744668,Human_RBP_ID_23935953,Human_RBP_ID_24381419,Human_RBP_ID_27841063 RMVar_hsa_circ_80692,RMVar_hsa_circ_117041,RMVar_hsa_circ_81712,RMVar_hsa_circ_213011,RMVar_hsa_circ_213012,RMVar_hsa_circ_335831,RMVar_hsa_circ_213013 89676 RMVar_ID_89676 Human_SNP_ID_698959057 m1A Human chr22 - 20131973 20131973 20131973 CCGTGGCCACCGGGATGTACTTGGCGGGTTTGAGGCGCGTCCCGGGGCTGCGGGGCATCCTGGGC CCGTGGCCACCGGGATGTACTTGGCGGGTTTGTGGCGCGTCCCGGGGCTGCGGGGCATCCTGGGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20131924..20132025 26863196 MeRIP-seq:(Medium) rs368332591 Functional Loss SNV dbSNP153 33..33 33 - - - 89677 RMVar_ID_89677 Human_SNP_ID_698961591 m1A Human chr22 - 20140922 20140922 20140922 GCAGCTCGGTCCAGGAGTTCAGGCCTAAGGAAAGGCGGCTTCAAACTCACCGCGAGCGGCAGCCG GCAGCTCGGTCCAGGAGTTCAGGCCTAAGGAAGGGCGGCTTCAAACTCACCGCGAGCGGCAGCCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20140619..20141335 32194978 MeRIP-seq:(Medium) rs1224751511 Functional Loss SNV dbSNP153 33..33 33 - - - 89678 RMVar_ID_89678 Human_SNP_ID_698962299 m1A Human chr22 - 20143127 20143127 20143127 TGCAGGTAGGGTGAGTGGTATCCGGCCACGCCAACTGCTGGGTGGGCAGGGCAGGCGTGGCCACC TGCAGGTAGGGTGAGTGGTATCCGGCCACGCCCACTGCTGGGTGGGCAGGGCAGGCGTGGCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20143078..20143355 26863196 MeRIP-seq:(Medium) rs1336185026 Functional Loss SNV dbSNP153 33..33 33 - - - 89679 RMVar_ID_89679 Human_SNP_ID_698962311 m1A Human chr22 - 20143152 20143152 20143152 TGGCGGGTCGCCCGTTGCCCCAGGATGCAGGTAGGGTGAGTGGTATCCGGCCACGCCAACTGCTG TGGCGGGTCGCCCGTTGCCCCAGGATGCAGGTCGGGTGAGTGGTATCCGGCCACGCCAACTGCTG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:20143101..20143247 26863196 MeRIP-seq:(Medium) rs773211725 Functional Loss SNV dbSNP153 33..33 33 - - - 89680 RMVar_ID_89680 Human_SNP_ID_698962565 m1A Human chr22 + 20143591 20143591 20143591 CTCCTCCCTGCAGGCTGATCAGGCCAGCAGCAACGCCCCGGGGCCCCGGCCCAGCAGTGGCTCAC CTCCTCCCTGCAGGCTGATCAGGCCAGCAGCAGCGCCCCGGGGCCCCGGCCCAGCAGTGGCTCAC A G ZDHHC8 Ensembl:ENSG00000099904 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20143544..20143712 26863196 MeRIP-seq:(Medium) rs753869821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931568 RMVar_hsa_circ_294298,RMVar_hsa_circ_213017,RMVar_hsa_circ_378537,RMVar_hsa_circ_122003,RMVar_hsa_circ_213020 89681 RMVar_ID_89681 Human_SNP_ID_698963112 m1A Human chr22 + 20145456 20145455 20145456 ATGGTGCCACGGGGACCAGGACCCCACAGCGCACCCCCCCTCCCCACCAACTTCTCTGCCCCAGG ATGGTGCCACGGGGACCAGGACCCCACAGCGC_CCCCCCCTCCCCACCAACTTCTCTGCCCCAGG CA C ZDHHC8 Ensembl:ENSG00000099904 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20145409..20145565 26863196 MeRIP-seq:(Medium) rs1159578984 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_575656,Human_RBP_ID_27491745 89682 RMVar_ID_89682 Human_SNP_ID_698963133 m1A Human chr22 + 20145495 20145495 20145495 CTCCCCACCAACTTCTCTGCCCCAGGGACCCGAGGCCACCCCAGCCTGGTGTGGACCCATCGGCG CTCCCCACCAACTTCTCTGCCCCAGGGACCCGCGGCCACCCCAGCCTGGTGTGGACCCATCGGCG A C ZDHHC8 Ensembl:ENSG00000099904 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20145310..20146360 32194978 MeRIP-seq:(Medium) rs545639855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929720,Human_RBP_ID_5119878 89683 RMVar_ID_89683 Human_SNP_ID_698963134 m1A Human chr22 + 20145495 20145495 20145495 CTCCCCACCAACTTCTCTGCCCCAGGGACCCGAGGCCACCCCAGCCTGGTGTGGACCCATCGGCG CTCCCCACCAACTTCTCTGCCCCAGGGACCCGTGGCCACCCCAGCCTGGTGTGGACCCATCGGCG A T ZDHHC8 Ensembl:ENSG00000099904 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20145310..20146360 32194978 MeRIP-seq:(Medium) rs545639855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929720,Human_RBP_ID_5119878 89684 RMVar_ID_89684 Human_SNP_ID_698963301 m1A Human chr22 - 20146064 20146063 20146065 GAAAGGGACAGCGGCGGCCGGAGCACTGACACATCAGACACGGCGCGGCAGCACAGCACACAGAC GAAAGGGACAGCGGCGGCCGGAGCACTGACA__TCAGACACGGCGCGGCAGCACAGCACACAGAC ATG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20146014..20146130 26863196 MeRIP-seq:(Medium) rs1053241673 Functional Loss DEL dbSNP153 32..33 33 - - - 89685 RMVar_ID_89685 Human_SNP_ID_698992315 m1A Human chr22 - 20243009 20243009 20243009 GCGTATGCTACAATGAGCCCAAGGTGACGACAAGCTGCCCCCAGCAGGGCCTGCAGGCTGTGCCC GCGTATGCTACAATGAGCCCAAGGTGACGACAGGCTGCCCCCAGCAGGGCCTGCAGGCTGTGCCC T C RTN4R Ensembl:ENSG00000040608 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:20242958..20243059 32194978 MeRIP-seq:(Medium) rs770557657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27491771 89686 RMVar_ID_89686 Human_SNP_ID_698999038 m1A Human chr22 - 20268152 20268146 20268152 GGCGGCGCCTGGATGCGGACCCGGCCGCGGGGAGACGGGCGCCCGCCCCGAAACGACTTTCAGTC GGCGGCGCCTGGATGCGGACCCGGCCGCGGGG______GCGCCCGCCCCGAAACGACTTTCAGTC CCCGTCT C RTN4R Ensembl:ENSG00000040608 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20268116..20268307 26863196 MeRIP-seq:(Medium) rs200304149 Functional Loss DEL dbSNP153 33..38 33 - - - Human_Splice_Rec_2139389 89687 RMVar_ID_89687 Human_SNP_ID_699012630 m1A Human chr22 + 20319979 20319979 20319979 ACCGTCCGCCACCTCCTCCAAGGCGGCCGCGTAGCGCTCCATGGCGCGGACGCCCGCTAGCCGCC ACCGTCCGCCACCTCCTCCAAGGCGGCCGCGTGGCGCTCCATGGCGCGGACGCCCGCTAGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:20319930..20320005;chr22:20319930..20320017;chr22:20319929..20320016 26863196 MeRIP-seq:(Medium) rs770389382 Functional Loss SNV dbSNP153 33..33 33 - - - 89688 RMVar_ID_89688 Human_SNP_ID_699012672 m1A Human chr22 + 20320022 20320022 20320022 GCGCGGACGCCCGCTAGCCGCCGGCGGCGGCGACGAGCTCCCCCAGCTTCACGACATCCCGAGCG GCGCGGACGCCCGCTAGCCGCCGGCGGCGGCGGCGAGCTCCCCCAGCTTCACGACATCCCGAGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20319916..20320050 26863196 MeRIP-seq:(Medium) rs1233946725 Functional Loss SNV dbSNP153 33..33 33 - - - 89689 RMVar_ID_89689 Human_SNP_ID_699012880 m1A Human chr22 - 20320735 20320735 20320735 CCTCTCGCCCACCCACCTGACCTGACTCTGGCAGGGCCTTTGCAGGAGCCATTCCTCCACCCGAG CCTCTCGCCCACCCACCTGACCTGACTCTGGCGGGGCCTTTGCAGGAGCCATTCCTCCACCCGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20320695..20320891 26863196 MeRIP-seq:(Medium) rs1237008617 Functional Loss SNV dbSNP153 33..33 33 - - - 89690 RMVar_ID_89690 Human_SNP_ID_699037320 m1A Human chr22 - 20394418 20394418 20394418 GCTGAGGTGGGGTTCAGGCCGGCTCCGCAGATACCCACTCCCCACACCAGGCTCAGCCCCATGCT GCTGAGGTGGGGTTCAGGCCGGCTCCGCAGATTCCCACTCCCCACACCAGGCTCAGCCCCATGCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20394367..20394463 26863196 MeRIP-seq:(Medium) rs1426007760 Functional Loss SNV dbSNP153 33..33 33 - - - 89691 RMVar_ID_89691 Human_SNP_ID_699039019 m1A Human chr22 - 20401352 20401352 20401352 GCCTCTGCTCACCTGGACAGGGCCCTCTGGGGACTTCCCTCTGCATGCTCCATGGCTCCTCGCCT GCCTCTGCTCACCTGGACAGGGCCCTCTGGGGGCTTCCCTCTGCATGCTCCATGGCTCCTCGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20401281..20405386 32194978 MeRIP-seq:(Medium) rs1482780984 Functional Loss SNV dbSNP153 33..33 33 - - - 89692 RMVar_ID_89692 Human_SNP_ID_699047123 m1A Human chr22 + 20429127 20429127 20429127 GCGCCCACGCACATCAACACTCAAGGTCCCCCATTTCCTCACTGAGATCTGGACCCCCTCACACC GCGCCCACGCACATCAACACTCAAGGTCCCCCCTTTCCTCACTGAGATCTGGACCCCCTCACACC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20429016..20429187 26863196 MeRIP-seq:(Medium) rs1035202105 Functional Loss SNV dbSNP153 33..33 33 - - - 89693 RMVar_ID_89693 Human_SNP_ID_699047366 m1A Human chr22 + 20429629 20429629 20429629 AGACGAGCAGGACGAGCAGCGCGCCCGCGCCCATCACGCCCTTGCGCTGGTTGGTTTCTGTAGGG AGACGAGCAGGACGAGCAGCGCGCCCGCGCCCGTCACGCCCTTGCGCTGGTTGGTTTCTGTAGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20429578..20429854 32194978 MeRIP-seq:(Medium) rs1407630978 Functional Loss SNV dbSNP153 33..33 33 - - - 89694 RMVar_ID_89694 Human_SNP_ID_699048332 m1A Human chr22 - 20431950 20431950 20431950 GGTGCCCACGTGCTGCGCTGGCTGGAGGCAGCAAGGGGACGAGTGTGGGATTGGTGAGTGGGTCA GGTGCCCACGTGCTGCGCTGGCTGGAGGCAGCTAGGGGACGAGTGTGGGATTGGTGAGTGGGTCA T A AC007731.5,SCARF2 Ensembl:ENSG00000277971,Ensembl:ENSG00000244486 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20431937..20432009 26863196 MeRIP-seq:(Medium) rs1363942544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2139578,Human_Splice_Rec_2139579,Human_Splice_Rec_2139598,Human_Splice_Rec_2139599 RMVar_hsa_circ_213031,RMVar_hsa_circ_85274 89695 RMVar_ID_89695 Human_SNP_ID_699049191 m1A Human chr22 - 20435539 20435539 20435539 GGAGGGGCTGGCGGAGGAGCTGCCAGAGAGTGAGGGTGGGCAGGCCACCGTGGGCTGCCACTGCT GGAGGGGCTGGCGGAGGAGCTGCCAGAGAGTGTGGGTGGGCAGGCCACCGTGGGCTGCCACTGCT T A AC007731.5,SCARF2 Ensembl:ENSG00000277971,Ensembl:ENSG00000244486 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20435528..20435703 26863196 MeRIP-seq:(Medium) rs1190078467 Functional Loss SNV dbSNP153 33..33 33 - - - 89696 RMVar_ID_89696 Human_SNP_ID_699050958 m1A Human chr22 + 20442066 20442066 20442066 CCCCAGCCTCCCTTCCCTCTGATGCCAGGCACAGGGAGCCTAGTCCTCACTGGAGTTGTCAAACT CCCCAGCCTCCCTTCCCTCTGATGCCAGGCACGGGGAGCCTAGTCCTCACTGGAGTTGTCAAACT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20442017..20442118 32194978 MeRIP-seq:(Medium) rs757453212 Functional Loss SNV dbSNP153 33..33 33 - - - 89697 RMVar_ID_89697 Human_SNP_ID_699050987 m1A Human chr22 - 20442165 20442165 20442165 CCCGCTCCCTGCTCCTTGAGCCGCCCCGCGGGACCCCTGACCGCAGCCAGGCCGACCCGGACTTT CCCGCTCCCTGCTCCTTGAGCCGCCCCGCGGGGCCCCTGACCGCAGCCAGGCCGACCCGGACTTT T C KLHL22,AC007731.5 Ensembl:ENSG00000099910,Ensembl:ENSG00000277971 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:20442117..20442268 32194978 MeRIP-seq:(Medium) rs917227417 Functional Loss SNV dbSNP153 33..33 33 - - - 89698 RMVar_ID_89698 Human_SNP_ID_699052099 m1A Human chr22 - 20446617 20446617 20446617 GAGGGGAAGATGTATATCACCTGCGGCCGCAGAGGGGAGGATTACCTGAAAGAGACACACTGCTA GAGGGGAAGATGTATATCACCTGCGGCCGCAGGGGGGAGGATTACCTGAAAGAGACACACTGCTA T C KLHL22,AC007731.5 Ensembl:ENSG00000099910,Ensembl:ENSG00000277971 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20442417..20446622 32194978 MeRIP-seq:(Medium) rs776516851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17063979 Human_Splice_Rec_2139642 RMVar_hsa_circ_213033,RMVar_hsa_circ_304935,RMVar_hsa_circ_345877,RMVar_hsa_circ_337290,RMVar_hsa_circ_12450,RMVar_hsa_circ_276817,RMVar_hsa_circ_213034 89699 RMVar_ID_89699 Human_SNP_ID_699063099 m1A Human chr22 + 20490816 20490816 20490816 TCTGATCTGACAGGAGGTGGAGCTCAGGTGGTAATGCTGGATCACCCTCCACTCACCTCCTGTTG TCTGATCTGACAGGAGGTGGAGCTCAGGTGGTGATGCTGGATCACCCTCCACTCACCTCCTGTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20490795..20490898 32194978 MeRIP-seq:(Medium) rs971140408 Functional Loss SNV dbSNP153 33..33 33 - - - 89700 RMVar_ID_89700 Human_SNP_ID_699063322 m1A Human chr22 + 20491891 20491891 20491891 GAGTCTGCCTCCAGGACCTGGGACCTCTATCCAGCCACCCACCCATTCCTTTCCCCCTCCTGGGC GAGTCTGCCTCCAGGACCTGGGACCTCTATCCGGCCACCCACCCATTCCTTTCCCCCTCCTGGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:20491843..20492075 26863196 MeRIP-seq:(Medium) rs1052372324 Functional Loss SNV dbSNP153 33..33 33 - - - 89701 RMVar_ID_89701 Human_SNP_ID_699063362 m1A Human chr22 - 20492050 20492048 20492050 GGCTCGAGCAGGGTGTGTGGGATGAAAGAGAGAGGTCAGAAAAGGGAGAATTATCATAGAGCAGA GGCTCGAGCAGGGTGTGTGGGATGAAAGAGAG__GTCAGAAAAGGGAGAATTATCATAGAGCAGA CCT C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20491786..20493191 26863196 MeRIP-seq:(Medium) rs144681376 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3678350,Human_RBP_ID_17069194,Human_RBP_ID_23010974,Human_RBP_ID_23936159 89702 RMVar_ID_89702 Human_SNP_ID_699063363 m1A Human chr22 - 20492050 20492050 20492050 GGCTCGAGCAGGGTGTGTGGGATGAAAGAGAGAGGTCAGAAAAGGGAGAATTATCATAGAGCAGA GGCTCGAGCAGGGTGTGTGGGATGAAAGAGAGGGGTCAGAAAAGGGAGAATTATCATAGAGCAGA T C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20491786..20493191 26863196 MeRIP-seq:(Medium) rs770129110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3678350,Human_RBP_ID_17069194,Human_RBP_ID_23010974,Human_RBP_ID_23936159 89703 RMVar_ID_89703 Human_SNP_ID_699063364 m1A Human chr22 - 20492054 20492054 20492054 GATGGGCTCGAGCAGGGTGTGTGGGATGAAAGAGAGAGGTCAGAAAAGGGAGAATTATCATAGAG GATGGGCTCGAGCAGGGTGTGTGGGATGAAAGCGAGAGGTCAGAAAAGGGAGAATTATCATAGAG T G KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20491553..20493191 26863196 MeRIP-seq:(Medium) rs776073332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3678350,Human_RBP_ID_23936159 89704 RMVar_ID_89704 Human_SNP_ID_699067721 m1A Human chr22 + 20507650 20507650 20507650 GACTGAGGCGGCGGCGGTGGCGGCCAAGCGGGATACGGGCGGCGGGAGCTGGGGAACAGGCATGG GACTGAGGCGGCGGCGGTGGCGGCCAAGCGGGTTACGGGCGGCGGGAGCTGGGGAACAGGCATGG A T MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20507601..20507771 26863196 MeRIP-seq:(Medium) rs754228525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782127,Human_RBP_ID_7063210,Human_RBP_ID_9332673,Human_RBP_ID_18193990,Human_RBP_ID_22086288,Human_RBP_ID_25655978,Human_RBP_ID_26345112 Human_Splice_Rec_2139713,Human_Splice_Rec_2139719,Human_Splice_Rec_2139723,Human_Splice_Rec_2139735,Human_Splice_Rec_2139767,Human_Splice_Rec_2139777,Human_Splice_Rec_2139809,Human_Splice_Rec_2139843,Human_Splice_Rec_2139851,Human_Splice_Rec_2139883 89705 RMVar_ID_89705 Human_SNP_ID_699067722 m1A Human chr22 - 20507651 20507651 20507651 TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTATCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTTTCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20507601..20507750 26863196 MeRIP-seq:(Medium) rs897292439 Functional Loss SNV dbSNP153 33..33 33 - - - 89706 RMVar_ID_89706 Human_SNP_ID_699067723 m1A Human chr22 - 20507651 20507651 20507651 TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTATCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTGTCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20507601..20507750 26863196 MeRIP-seq:(Medium) rs897292439 Functional Loss SNV dbSNP153 33..33 33 - - - 89707 RMVar_ID_89707 Human_SNP_ID_699067741 m1A Human chr22 + 20507675 20507675 20507675 AAGCGGGATACGGGCGGCGGGAGCTGGGGAACAGGCATGGACGTTTCCGGGCAAGAGACCGACTG AAGCGGGATACGGGCGGCGGGAGCTGGGGAACCGGCATGGACGTTTCCGGGCAAGAGACCGACTG A C MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:20507601..20507803;chr22:20507576..20507815 26863196 MeRIP-seq:(Medium) rs758630447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246487,Human_RBP_ID_7063210,Human_RBP_ID_9332673,Human_RBP_ID_14400807,Human_RBP_ID_18193990,Human_RBP_ID_19008570,Human_RBP_ID_26345112 Human_Splice_Rec_2139713,Human_Splice_Rec_2139719,Human_Splice_Rec_2139723,Human_Splice_Rec_2139735,Human_Splice_Rec_2139767,Human_Splice_Rec_2139777,Human_Splice_Rec_2139809,Human_Splice_Rec_2139843,Human_Splice_Rec_2139851,Human_Splice_Rec_2139883 89708 RMVar_ID_89708 Human_SNP_ID_699067742 m1A Human chr22 + 20507675 20507675 20507675 AAGCGGGATACGGGCGGCGGGAGCTGGGGAACAGGCATGGACGTTTCCGGGCAAGAGACCGACTG AAGCGGGATACGGGCGGCGGGAGCTGGGGAACGGGCATGGACGTTTCCGGGCAAGAGACCGACTG A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:20507601..20507803;chr22:20507576..20507815 26863196 MeRIP-seq:(Medium) rs758630447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246487,Human_RBP_ID_7063210,Human_RBP_ID_9332673,Human_RBP_ID_14400807,Human_RBP_ID_18193990,Human_RBP_ID_19008570,Human_RBP_ID_26345112 Human_Splice_Rec_2139713,Human_Splice_Rec_2139719,Human_Splice_Rec_2139723,Human_Splice_Rec_2139735,Human_Splice_Rec_2139767,Human_Splice_Rec_2139777,Human_Splice_Rec_2139809,Human_Splice_Rec_2139843,Human_Splice_Rec_2139851,Human_Splice_Rec_2139883 89709 RMVar_ID_89709 Human_SNP_ID_699067882 m1A Human chr22 + 20508067 20508067 20508067 CCCCCGCTTTTTGAACCACACTGAATAGGGAAAGGGAGAGAAGCAGCCGGCTGTAGTGGGTTTAG CCCCCGCTTTTTGAACCACACTGAATAGGGAAGGGGAGAGAAGCAGCCGGCTGTAGTGGGTTTAG A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20508063..20508370 26863196 MeRIP-seq:(Medium) rs1214951888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3675986 89710 RMVar_ID_89710 Human_SNP_ID_699071682 m1A Human chr22 + 20522723 20522723 20522723 TGAAATTTCCAACAGTCAGTGGGAGATGGGGGAAGCAAACCTGGGAAGAGCAGCCTGCTGCAGGA TGAAATTTCCAACAGTCAGTGGGAGATGGGGGGAGCAAACCTGGGAAGAGCAGCCTGCTGCAGGA A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20522720..20522858 26863196 MeRIP-seq:(Medium) rs1249512985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21986190,Human_RBP_ID_23285889,Human_RBP_ID_23936198 89711 RMVar_ID_89711 Human_SNP_ID_699075405 m1A Human chr22 + 20537065 20537065 20537065 TGCTATGCAGGGCCTGTTGGCCAGGGCCCTGCAGCGGTGGAGTCACTGGTGTGTGCAAACGTCTC TGCTATGCAGGGCCTGTTGGCCAGGGCCCTGCGGCGGTGGAGTCACTGGTGTGTGCAAACGTCTC A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20537061..20537136 26863196 MeRIP-seq:(Medium) rs1018121172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22550551,Human_RBP_ID_22674016 89712 RMVar_ID_89712 Human_SNP_ID_699083276 m1A Human chr22 - 20566631 20566631 20566631 GTGTGATGCATCTGCTGCAGCTGCTGGGGCAGAGCCTGGGAGGGCGGAGGCTGTGGCTGCTGCAT GTGTGATGCATCTGCTGCAGCTGCTGGGGCAGTGCCTGGGAGGGCGGAGGCTGTGGCTGCTGCAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20566537..20566800 26863196 MeRIP-seq:(Medium) rs1277614100 Functional Loss SNV dbSNP153 33..33 33 - - - 89713 RMVar_ID_89713 Human_SNP_ID_699083284 m1A Human chr22 + 20566651 20566651 20566651 GCCCTCCCAGGCTCTGCCCCAGCAGCTGCAGCAGATGCATCACACACAGCACCACCAGCCGCCAC GCCCTCCCAGGCTCTGCCCCAGCAGCTGCAGCTGATGCATCACACACAGCACCACCAGCCGCCAC A T MED15 Ensembl:ENSG00000099917 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20566601..20566759 26863196 MeRIP-seq:(Medium) rs149450332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833462,Human_RBP_ID_17399693,Human_RBP_ID_22533803 RMVar_hsa_circ_8148,RMVar_hsa_circ_321131,RMVar_hsa_circ_265322,RMVar_hsa_circ_31298,RMVar_hsa_circ_53337,RMVar_hsa_circ_326985,RMVar_hsa_circ_313511,RMVar_hsa_circ_282443,RMVar_hsa_circ_213046,RMVar_hsa_circ_304687,RMVar_hsa_circ_213045,RMVar_hsa_circ_317420,RMVar_hsa_circ_213048,RMVar_hsa_circ_305148 89714 RMVar_ID_89714 Human_SNP_ID_699083293 m1A Human chr22 + 20566693 20566685 20566694 CACACAGCACCACCAGCCGCCACCACAGCCCCAGCAGCCTCCAGTTGCTCAGAACCAACCATCAC CACACAGCACCACCAGCCGCCACCA_________CAGCCTCCAGTTGCTCAGAACCAACCATCAC ACAGCCCCAG A MED15 Ensembl:ENSG00000099917 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:20566643..20566749 26863196 MeRIP-seq:(Medium) rs1298558309 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_780984,Human_RBP_ID_17285042,Human_RBP_ID_17399694,Human_RBP_ID_20716833 Human_miRNA_ID_1036616,Human_miRNA_ID_1359411,Human_miRNA_ID_1396643,Human_miRNA_ID_2686570,Human_miRNA_ID_2716701,Human_miRNA_ID_3052683 RMVar_hsa_circ_8148,RMVar_hsa_circ_321131,RMVar_hsa_circ_265322,RMVar_hsa_circ_31298,RMVar_hsa_circ_53337,RMVar_hsa_circ_326985,RMVar_hsa_circ_313511,RMVar_hsa_circ_282443,RMVar_hsa_circ_213046,RMVar_hsa_circ_304687,RMVar_hsa_circ_213045,RMVar_hsa_circ_317420,RMVar_hsa_circ_213048,RMVar_hsa_circ_305148 89715 RMVar_ID_89715 Human_SNP_ID_699087790 m1A Human chr22 - 20582872 20582872 20582872 GGCTCTGGGAGGGCTGCGGTGAGGGGCTGGGCAGGAAGCTACTGGGAGATGGGGCAGGGCCAGAG GGCTCTGGGAGGGCTGCGGTGAGGGGCTGGGCGGGAAGCTACTGGGAGATGGGGCAGGGCCAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20582601..20582950 26863196 MeRIP-seq:(Medium) rs1477413858 Functional Loss SNV dbSNP153 33..33 33 - - - 89716 RMVar_ID_89716 Human_SNP_ID_699087916 m1A Human chr22 + 20583206 20583206 20583206 GGACAAGCTGAAGCAGCTGTCGAAGTACATCGAGCCCCTGCGCCGCATGATCAACAAGATCGACA GGACAAGCTGAAGCAGCTGTCGAAGTACATCGCGCCCCTGCGCCGCATGATCAACAAGATCGACA A C MED15 Ensembl:ENSG00000099917 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20583160..20583420 26863196 MeRIP-seq:(Medium) rs879105489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9124567,Human_RBP_ID_23115705 Human_Splice_Rec_2139754,Human_Splice_Rec_2139755,Human_Splice_Rec_2139796,Human_Splice_Rec_2139797,Human_Splice_Rec_2139830,Human_Splice_Rec_2139831,Human_Splice_Rec_2139870,Human_Splice_Rec_2139871,Human_Splice_Rec_2139900,Human_Splice_Rec_2139901,Human_Splice_Rec_2140012,Human_Splice_Rec_2140013,Human_Splice_Rec_2140030,Human_Splice_Rec_2140036,Human_Splice_Rec_2140037,Human_Splice_Rec_2140052,Human_Splice_Rec_2140053,Human_Splice_Rec_2140065,Human_Splice_Rec_2140070,Human_Splice_Rec_2140071 RMVar_hsa_circ_265322 89717 RMVar_ID_89717 Human_SNP_ID_699124059 m1A Human chr22 + 20702842 20702842 20702842 TGAGGCCGGCACCGCCCCAGGACCCTGTCCGCAGGAGCAGCACAGCAGGCAGCTGCAGGGCAGTG TGAGGCCGGCACCGCCCCAGGACCCTGTCCGCTGGAGCAGCACAGCAGGCAGCTGCAGGGCAGTG A T TMEM191A Ensembl:ENSG00000226287 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20702813..20702891 26863196 MeRIP-seq:(Medium) rs1013133613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2140165,Human_Splice_Rec_2140192,Human_Splice_Rec_2140193,Human_Splice_Rec_2140205 89718 RMVar_ID_89718 Human_SNP_ID_699124061 m1A Human chr22 + 20702848 20702848 20702848 CGGCACCGCCCCAGGACCCTGTCCGCAGGAGCAGCACAGCAGGCAGCTGCAGGGCAGTGGGAGGA CGGCACCGCCCCAGGACCCTGTCCGCAGGAGCGGCACAGCAGGCAGCTGCAGGGCAGTGGGAGGA A G TMEM191A Ensembl:ENSG00000226287 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20702796..20703060 26863196 MeRIP-seq:(Medium) rs1023164296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2140164,Human_Splice_Rec_2140165,Human_Splice_Rec_2140192,Human_Splice_Rec_2140193,Human_Splice_Rec_2140205 89719 RMVar_ID_89719 Human_SNP_ID_699128398 m1A Human chr22 - 20717719 20717719 20717719 GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGAAGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGAGGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG T C PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2845533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962072,Human_RBP_ID_8865560,Human_RBP_ID_19007660 Human_Splice_Rec_2140348,Human_Splice_Rec_2140349,Human_Splice_Rec_2140372,Human_Splice_Rec_2140373,Human_Splice_Rec_2140410,Human_Splice_Rec_2140411,Human_Splice_Rec_2140438,Human_Splice_Rec_2140439,Human_Splice_Rec_2140458,Human_Splice_Rec_2140459,Human_Splice_Rec_2140485 Human_miRNA_ID_2751350 RMVar_hsa_circ_98874,RMVar_hsa_circ_123980,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213052,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_115654,RMVar_hsa_circ_213056,RMVar_hsa_circ_127180,RMVar_hsa_circ_92859,RMVar_hsa_circ_213059,RMVar_hsa_circ_213060,RMVar_hsa_circ_108566,RMVar_hsa_circ_213061,RMVar_hsa_circ_213062,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_100044,RMVar_hsa_circ_213064,RMVar_hsa_circ_213065,RMVar_hsa_circ_213067,RMVar_hsa_circ_213066,RMVar_hsa_circ_125805,RMVar_hsa_circ_83593,RMVar_hsa_circ_328224,RMVar_hsa_circ_365537 89720 RMVar_ID_89720 Human_SNP_ID_699128399 m1A Human chr22 - 20717719 20717719 20717719 GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGAAGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGACGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG T G PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2845533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962072,Human_RBP_ID_8865560,Human_RBP_ID_19007660 Human_Splice_Rec_2140348,Human_Splice_Rec_2140349,Human_Splice_Rec_2140372,Human_Splice_Rec_2140373,Human_Splice_Rec_2140410,Human_Splice_Rec_2140411,Human_Splice_Rec_2140438,Human_Splice_Rec_2140439,Human_Splice_Rec_2140458,Human_Splice_Rec_2140459,Human_Splice_Rec_2140485 Human_miRNA_ID_2751350 RMVar_hsa_circ_98874,RMVar_hsa_circ_123980,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213052,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_115654,RMVar_hsa_circ_213056,RMVar_hsa_circ_127180,RMVar_hsa_circ_92859,RMVar_hsa_circ_213059,RMVar_hsa_circ_213060,RMVar_hsa_circ_108566,RMVar_hsa_circ_213061,RMVar_hsa_circ_213062,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_100044,RMVar_hsa_circ_213064,RMVar_hsa_circ_213065,RMVar_hsa_circ_213067,RMVar_hsa_circ_213066,RMVar_hsa_circ_125805,RMVar_hsa_circ_83593,RMVar_hsa_circ_328224,RMVar_hsa_circ_365537 89721 RMVar_ID_89721 Human_SNP_ID_699166432 m1A Human chr22 + 20858243 20858242 20858243 CCTGGTCCTCGGCTCATCCCACTGCTCCGCACAGCCGCCCACGATCCAGCCTCCACCTCCGCGAT CCTGGTCCTCGGCTCATCCCACTGCTCCGCAC_GCCGCCCACGATCCAGCCTCCACCTCCGCGAT CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20858237..20858561 26863196 MeRIP-seq:(Medium) rs1257515905 Functional Loss DEL dbSNP153 33..33 33 - - - 89722 RMVar_ID_89722 Human_SNP_ID_699166481 m1A Human chr22 + 20858392 20858392 20858392 GCCGACCCTTCCCCCACGGTCCCTCTCTCTTCACCAGCCCCTCCCACTAGGGCCTCCTTCCCCCG GCCGACCCTTCCCCCACGGTCCCTCTCTCTTCCCCAGCCCCTCCCACTAGGGCCTCCTTCCCCCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20858234..20858559 26863196 MeRIP-seq:(Medium) rs553480648 Functional Loss SNV dbSNP153 33..33 33 - - - 89723 RMVar_ID_89723 Human_SNP_ID_699166622 m1A Human chr22 - 20858684 20858672 20858684 GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGGAGGCGGCGGCGGCTGCTCCGGCTCCGGCTCCAG GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGG____________CTGCTCCGGCTCCGGCTCCAG GCCGCCGCCGCCT G PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:20858635..20858761 26863196 MeRIP-seq:(Medium) rs551553536 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_246392,Human_RBP_ID_4708065,Human_RBP_ID_17146934 RMVar_hsa_circ_120791,RMVar_hsa_circ_213104,RMVar_hsa_circ_269194,RMVar_hsa_circ_213122,RMVar_hsa_circ_91401 89724 RMVar_ID_89724 Human_SNP_ID_699166638 m1A Human chr22 - 20858684 20858681 20858684 GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGGAGGCGGCGGCGGCTGCTCCGGCTCCGGCTCCAG GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGG___CGGCGGCGGCTGCTCCGGCTCCGGCTCCAG GCCT G PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:20858635..20858761 26863196 MeRIP-seq:(Medium) rs1428059975 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_246392,Human_RBP_ID_4708065,Human_RBP_ID_17146934 RMVar_hsa_circ_120791,RMVar_hsa_circ_213104,RMVar_hsa_circ_269194,RMVar_hsa_circ_213122,RMVar_hsa_circ_91401 89725 RMVar_ID_89725 Human_SNP_ID_699166639 m1A Human chr22 - 20858684 20858684 20858684 GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGGAGGCGGCGGCGGCTGCTCCGGCTCCGGCTCCAG GCCCCGGCCCGGGGAGGCGGAGGCGGAGGCGGCGGCGGCGGCGGCTGCTCCGGCTCCGGCTCCAG T G PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:20858635..20858761 26863196 MeRIP-seq:(Medium) rs1264411713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246392,Human_RBP_ID_4708065,Human_RBP_ID_17146934 RMVar_hsa_circ_120791,RMVar_hsa_circ_213104,RMVar_hsa_circ_269194,RMVar_hsa_circ_213122,RMVar_hsa_circ_91401 89726 RMVar_ID_89726 Human_SNP_ID_699166686 m1A Human chr22 - 20858746 20858746 20858746 GCTCGCGGGCCAGGAGCGGGGAGCCGGCGGGCAGCGCCGCGGCTCGTGAGGTGATGGCGGCGGCC GCTCGCGGGCCAGGAGCGGGGAGCCGGCGGGCGGCGCCGCGGCTCGTGAGGTGATGGCGGCGGCC T C PI4KA Ensembl:ENSG00000241973 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr22:20858658..20858758 26863410 MeRIP-seq:(Medium) rs971136724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4686792,Human_RBP_ID_8865595,Human_RBP_ID_17146934,Human_RBP_ID_18423697 RMVar_hsa_circ_120791,RMVar_hsa_circ_213104,RMVar_hsa_circ_269194,RMVar_hsa_circ_213122,RMVar_hsa_circ_91401 89727 RMVar_ID_89727 Human_SNP_ID_699169909 m1A Human chr22 + 20870475 20870475 20870475 TGTTTGGGGGGCTGGTCAATTACTTCAAATCCAAACCAGTAGAGACCCCACCTGAACAGAATGGC TGTTTGGGGGGCTGGTCAATTACTTCAAATCCGAACCAGTAGAGACCCCACCTGAACAGAATGGC A G SNAP29 Ensembl:ENSG00000099940 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20870426..20870585 26863196 MeRIP-seq:(Medium) rs779541145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1028423,Human_RBP_ID_8116818,Human_RBP_ID_9391987,Human_RBP_ID_14404078,Human_RBP_ID_17982484,Human_RBP_ID_26345155 Human_Splice_Rec_2140593,Human_Splice_Rec_2140603 RMVar_hsa_circ_213127,RMVar_hsa_circ_112623,RMVar_hsa_circ_357062,RMVar_hsa_circ_213126,RMVar_hsa_circ_302221 89728 RMVar_ID_89728 Human_SNP_ID_699196793 m1A Human chr22 - 20966909 20966909 20966909 TGCCCAACAGCATATGGGGAAAGCAAGGGGTCAAGGTCCCATCAAGGTCAAGCAGCAGGGGCATC TGCCCAACAGCATATGGGGAAAGCAAGGGGTCGAGGTCCCATCAAGGTCAAGCAGCAGGGGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20966901..20967012 26863196 MeRIP-seq:(Medium) rs558893698 Functional Loss SNV dbSNP153 33..33 33 - - - 89729 RMVar_ID_89729 Human_SNP_ID_699201598 m1A Human chr22 - 20982362 20982362 20982362 CCCGTGCTGCCCGGTCCAGCCATCCCGGGTCCACGCCGGATCGGCCGCGCTGTAAGCCCAACTTG CCCGTGCTGCCCGGTCCAGCCATCCCGGGTCCGCGCCGGATCGGCCGCGCTGTAAGCCCAACTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20982315..20982476 26863196 MeRIP-seq:(Medium) rs916747043 Functional Loss SNV dbSNP153 33..33 33 - - - 89730 RMVar_ID_89730 Human_SNP_ID_699201604 m1A Human chr22 + 20982372 20982372 20982372 TTACAGCGCGGCCGATCCGGCGTGGACCCGGGATGGCTGGACCGGGCAGCACGGGGGGGCAGATC TTACAGCGCGGCCGATCCGGCGTGGACCCGGGTTGGCTGGACCGGGCAGCACGGGGGGGCAGATC A T AC002470.2,LZTR1 Ensembl:ENSG00000285314,Ensembl:ENSG00000099949 lincRNA,Protein coding intron,start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20982321..20982471 26863196 MeRIP-seq:(Medium) rs1569152752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679527,Human_RBP_ID_4708462,Human_RBP_ID_5205827,Human_RBP_ID_5324079,Human_RBP_ID_5600987,Human_RBP_ID_8865860,Human_RBP_ID_9300234,Human_RBP_ID_9332688,Human_RBP_ID_18423699,Human_RBP_ID_23936583,Human_RBP_ID_27841077 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135 89731 RMVar_ID_89731 Human_SNP_ID_699201607 m1A Human chr22 + 20982380 20982380 20982380 CGGCCGATCCGGCGTGGACCCGGGATGGCTGGACCGGGCAGCACGGGGGGGCAGATCGGGGCTGC CGGCCGATCCGGCGTGGACCCGGGATGGCTGGCCCGGGCAGCACGGGGGGGCAGATCGGGGCTGC A C AC002470.2,LZTR1 Ensembl:ENSG00000285314,Ensembl:ENSG00000099949 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:20982332..20982476;chr22:20982332..20982471 26863196 MeRIP-seq:(Medium) rs759169986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679527,Human_RBP_ID_4708462,Human_RBP_ID_5205827,Human_RBP_ID_5324079,Human_RBP_ID_5600987,Human_RBP_ID_8865860,Human_RBP_ID_9300234,Human_RBP_ID_9332688,Human_RBP_ID_18423699,Human_RBP_ID_23936583,Human_RBP_ID_27841077 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135 89732 RMVar_ID_89732 Human_SNP_ID_699201639 m1A Human chr22 - 20982418 20982418 20982418 TCGGGGCTACCTTGGACCGCGCGCCGCCTGCCAGGGCCGCAGCCCCGATCTGCCCCCCCGTGCTG TCGGGGCTACCTTGGACCGCGCGCCGCCTGCCTGGGCCGCAGCCCCGATCTGCCCCCCCGTGCTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:20982328..20982458 26863410 MeRIP-seq:(Medium) rs578100969 Functional Loss SNV dbSNP153 33..33 33 - - - 89733 RMVar_ID_89733 Human_SNP_ID_699201640 m1A Human chr22 - 20982418 20982418 20982418 TCGGGGCTACCTTGGACCGCGCGCCGCCTGCCAGGGCCGCAGCCCCGATCTGCCCCCCCGTGCTG TCGGGGCTACCTTGGACCGCGCGCCGCCTGCCGGGGCCGCAGCCCCGATCTGCCCCCCCGTGCTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:20982328..20982458 26863410 MeRIP-seq:(Medium) rs578100969 Functional Loss SNV dbSNP153 33..33 33 - - - 89734 RMVar_ID_89734 Human_SNP_ID_699205270 m1A Human chr22 - 20993756 20993756 20993756 GCAGGCAGAGCAGGGTGCGAGGACAGGCACCCACCTCACCCAGCACGAACTCCACGTCGCAGAAC GCAGGCAGAGCAGGGTGCGAGGACAGGCACCCCCCTCACCCAGCACGAACTCCACGTCGCAGAAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20993705..20994207 32194978 MeRIP-seq:(Medium) rs779146700 Functional Loss SNV dbSNP153 33..33 33 - - - 89735 RMVar_ID_89735 Human_SNP_ID_699206198 m1A Human chr22 + 20995551 20995551 20995551 TGAGACGCTGGGTGGTGGGCTGTGCGTGGGGCATAGTGCTTGAGTCGGCCAGGGCGCCGAGGGAG TGAGACGCTGGGTGGTGGGCTGTGCGTGGGGCGTAGTGCTTGAGTCGGCCAGGGCGCCGAGGGAG A G AC002470.2,LZTR1 Ensembl:ENSG00000285314,Ensembl:ENSG00000099949 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20995503..20995656 26863196 MeRIP-seq:(Medium) rs1335412871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10267,Human_RBP_ID_780849,Human_RBP_ID_929277,Human_RBP_ID_1614394,Human_RBP_ID_3676001,Human_RBP_ID_5205741,Human_RBP_ID_5601167,Human_RBP_ID_5654190,Human_RBP_ID_8118026,Human_RBP_ID_9332695,Human_RBP_ID_18952386,Human_RBP_ID_19114055,Human_RBP_ID_21985472,Human_RBP_ID_26345162,Human_RBP_ID_27841256 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135,RMVar_hsa_circ_123396,RMVar_hsa_circ_213137 89736 RMVar_ID_89736 Human_SNP_ID_699206328 m1A Human chr22 + 20995848 20995848 20995848 GTTGCTTGACGGGCACCCACGGCCAGCCCACAAGGCTATCCTGGCCGCCCGCTCCAGGTGGGTGG GTTGCTTGACGGGCACCCACGGCCAGCCCACAGGGCTATCCTGGCCGCCCGCTCCAGGTGGGTGG A G AC002470.2,LZTR1 Ensembl:ENSG00000285314,Ensembl:ENSG00000099949 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:20995801..20995850 32194978 MeRIP-seq:(Medium) rs1376902786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392638,Human_RBP_ID_19008644 Human_Splice_Rec_2140941,Human_Splice_Rec_2140997,Human_Splice_Rec_2141063,Human_Splice_Rec_2141101,Human_Splice_Rec_2141131,Human_Splice_Rec_2141149,Human_Splice_Rec_2141179,Human_Splice_Rec_2141193,Human_Splice_Rec_2141199,Human_Splice_Rec_2141207,Human_Splice_Rec_2141219,Human_Splice_Rec_2141222,Human_Splice_Rec_2141223,Human_Splice_Rec_2141229,Human_Splice_Rec_2141235 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135,RMVar_hsa_circ_123396,RMVar_hsa_circ_213137 89737 RMVar_ID_89737 Human_SNP_ID_699207069 m1A Human chr22 - 20997398 20997398 20997398 CATGCGCATAGCCGGTAGTCTTCTCAGTAGGCAGGGCAGGCAGGCACGGCGATTCTTCACAATGG CATGCGCATAGCCGGTAGTCTTCTCAGTAGGCGGGGCAGGCAGGCACGGCGATTCTTCACAATGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20997347..20997895 32194978 MeRIP-seq:(Medium) rs777690842 Functional Loss SNV dbSNP153 33..33 33 - - - 89738 RMVar_ID_89738 Human_SNP_ID_699207070 m1A Human chr22 - 20997398 20997398 20997398 CATGCGCATAGCCGGTAGTCTTCTCAGTAGGCAGGGCAGGCAGGCACGGCGATTCTTCACAATGG CATGCGCATAGCCGGTAGTCTTCTCAGTAGGCCGGGCAGGCAGGCACGGCGATTCTTCACAATGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20997347..20997895 32194978 MeRIP-seq:(Medium) rs777690842 Functional Loss SNV dbSNP153 33..33 33 - - - 89739 RMVar_ID_89739 Human_SNP_ID_699207466 m1A Human chr22 + 20998663 20998660 20998663 TGGCCTAGTGCAAGATGAGCTGGGAACAAGGGAGGAGAGAGCAGGAGCTGGGGCAGAGGCTGAGC TGGCCTAGTGCAAGATGAGCTGGGAACAAG___GGAGAGAGCAGGAGCTGGGGCAGAGGCTGAGC GGGA G LZTR1 Ensembl:ENSG00000099949 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20998614..20998937 26863196 MeRIP-seq:(Medium) rs756928647 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_833695,Human_RBP_ID_5529779,Human_RBP_ID_26345765,Human_RBP_ID_26499907,Human_RBP_ID_26770851 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135 89740 RMVar_ID_89740 Human_SNP_ID_699207849 m1A Human chr22 - 20999849 20999849 20999849 GAGGGGCTGCTGGACTGACCGAGGGGCTGCCCAGCAAGACTGCAGCCTCTTCCTCCCTCAGATCC GAGGGGCTGCTGGACTGACCGAGGGGCTGCCCGGCAAGACTGCAGCCTCTTCCTCCCTCAGATCC T C THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20999798..21000345 32194978 MeRIP-seq:(Medium) rs370198154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26499910,Human_RBP_ID_27304899 Human_miRNA_ID_1359309,Human_miRNA_ID_2611877,Human_miRNA_ID_2716703,Human_miRNA_ID_3052685 RMVar_hsa_circ_77909,RMVar_hsa_circ_213139 89741 RMVar_ID_89741 Human_SNP_ID_699208008 m1A Human chr22 - 21000130 21000130 21000130 GCGCCTGCCCCCACCCGCCGGAGCCTACATCCAGAATGAACACAGCTACCAGGTGGGCAGCGCCT GCGCCTGCCCCCACCCGCCGGAGCCTACATCCTGAATGAACACAGCTACCAGGTGGGCAGCGCCT T A THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21000081..21000357 26863196 MeRIP-seq:(Medium) rs766442228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17989144,Human_RBP_ID_26822267,Human_RBP_ID_27304904 RMVar_hsa_circ_77909,RMVar_hsa_circ_213139 89742 RMVar_ID_89742 Human_SNP_ID_699208009 m1A Human chr22 - 21000130 21000130 21000130 GCGCCTGCCCCCACCCGCCGGAGCCTACATCCAGAATGAACACAGCTACCAGGTGGGCAGCGCCT GCGCCTGCCCCCACCCGCCGGAGCCTACATCCCGAATGAACACAGCTACCAGGTGGGCAGCGCCT T G THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21000081..21000357 26863196 MeRIP-seq:(Medium) rs766442228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17989144,Human_RBP_ID_26822267,Human_RBP_ID_27304904 RMVar_hsa_circ_77909,RMVar_hsa_circ_213139 89743 RMVar_ID_89743 Human_SNP_ID_699208170 m1A Human chr22 - 21000424 21000424 21000424 AGTCTCTCTCTTCCCCCTTACCAGCTGCTCCGAGGGCCGAGGGCCCACAACTCCATTTTCTCCAC AGTCTCTCTCTTCCCCCTTACCAGCTGCTCCGGGGGCCGAGGGCCCACAACTCCATTTTCTCCAC T C THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21000376..21000450 26863196 MeRIP-seq:(Medium) rs1351828168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246266,Human_RBP_ID_929280,Human_RBP_ID_19111653,Human_RBP_ID_22084087,Human_RBP_ID_22674070,Human_RBP_ID_26822269 Human_Splice_Rec_2141242,Human_Splice_Rec_2141248,Human_Splice_Rec_2141250,Human_Splice_Rec_2141258,Human_Splice_Rec_2141262,Human_Splice_Rec_2141268,Human_Splice_Rec_2141272 RMVar_hsa_circ_77909,RMVar_hsa_circ_213139 89744 RMVar_ID_89744 Human_SNP_ID_699208463 m1A Human chr22 + 21001105 21001102 21001105 TCCTGTTTTCCCCTTGTGTCACAGGCACAGTGATCCTGGGGGTGGGTTTCACTGTGCAGAGCTGG TCCTGTTTTCCCCTTGTGTCACAGGCACAG___TCCTGGGGGTGGGTTTCACTGTGCAGAGCTGG GTGA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:21001103..21001204 32194978 MeRIP-seq:(Medium) rs1251672365 Functional Loss DEL dbSNP153 31..33 33 - - - 89745 RMVar_ID_89745 Human_SNP_ID_699208669 m1A Human chr22 - 21001665 21001665 21001665 AACGGTCCCGGCGGGACTGAATGCAGTCGGGAAGGGGAGGACGGGAAGTCTAGCCGGCTTGGACC AACGGTCCCGGCGGGACTGAATGCAGTCGGGAGGGGGAGGACGGGAAGTCTAGCCGGCTTGGACC T C THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:21001616..21001750 26863196 MeRIP-seq:(Medium) rs929794168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930179,Human_RBP_ID_4708468,Human_RBP_ID_9332698,Human_RBP_ID_9434126,Human_RBP_ID_18423844,Human_RBP_ID_22087120,Human_RBP_ID_23015381,Human_RBP_ID_26770952 RMVar_hsa_circ_269010 89746 RMVar_ID_89746 Human_SNP_ID_699208681 m1A Human chr22 - 21001703 21001703 21001703 CTGAGGAGGCTTGAACCTGTGGGTGGGAGGTGAAGCGGAACGGTCCCGGCGGGACTGAATGCAGT CTGAGGAGGCTTGAACCTGTGGGTGGGAGGTGGAGCGGAACGGTCCCGGCGGGACTGAATGCAGT T C THAP7 Ensembl:ENSG00000184436 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21001551..21001750 26863196 MeRIP-seq:(Medium) rs1476883546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575961,Human_RBP_ID_4708468,Human_RBP_ID_5119887,Human_RBP_ID_5324666,Human_RBP_ID_5504342,Human_RBP_ID_18423844,Human_RBP_ID_22087120,Human_RBP_ID_23015381 RMVar_hsa_circ_269010 89747 RMVar_ID_89747 Human_SNP_ID_699208827 m1A Human chr22 + 21001955 21001955 21001955 GCGGGAGTTAAGTCGCAAGCGGCTCTCCGGGCATCCGGAGGAGCCTCGCGCCTCCAGCCGCCGCT GCGGGAGTTAAGTCGCAAGCGGCTCTCCGGGCCTCCGGAGGAGCCTCGCGCCTCCAGCCGCCGCT A C THAP7-AS1 Ensembl:ENSG00000230513 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:21001897..21002047 26863410 MeRIP-seq:(Medium) rs1319555830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5298470 89748 RMVar_ID_89748 Human_SNP_ID_699209288 m1A Human chr22 + 21002818 21002818 21002818 CCGCCACCACGCCCGGCTAATTTGCAATACGGAAATTTTAATAGGTAATTAGCTCTCCTAGCGTT CCGCCACCACGCCCGGCTAATTTGCAATACGGCAATTTTAATAGGTAATTAGCTCTCCTAGCGTT A C THAP7-AS1 Ensembl:ENSG00000230513 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21002777..21002965 26863196 MeRIP-seq:(Medium) rs963634549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27032775 Human_Splice_Rec_2141275,Human_Splice_Rec_2141277,Human_Splice_Rec_2141279 89749 RMVar_ID_89749 Human_SNP_ID_699213042 m1A Human chr22 + 21015299 21015299 21015299 GATGACCAGGAACTGGCGGGTGGGCGCCCTGCAGAGGCTGCTGCAGTTTGGGATCGTGGTCTATG GATGACCAGGAACTGGCGGGTGGGCGCCCTGCCGAGGCTGCTGCAGTTTGGGATCGTGGTCTATG A C P2RX6 Ensembl:ENSG00000099957 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21015253..21015352 26863196 MeRIP-seq:(Medium) rs1284904631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22603116 Human_Splice_Rec_2141297,Human_Splice_Rec_2141359,Human_Splice_Rec_2141363,Human_Splice_Rec_2141371,Human_Splice_Rec_2141395 89750 RMVar_ID_89750 Human_SNP_ID_699299459 m1A Human chr22 + 21417559 21417559 21417559 CGGCGGGCGGAGCGCCGCCGCCGACGCACACGAGGTGAGGGGCGGCCTTGTGGGGCGGGGGGCGC CGGCGGGCGGAGCGCCGCCGCCGACGCACACGGGGTGAGGGGCGGCCTTGTGGGGCGGGGGGCGC A G HIC2 Ensembl:ENSG00000169635 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:21417534..21417607;chr22:21417550..21417663;chr22:21417532..21417600;chr22:21417516..21417603 26863196 MeRIP-seq:(Medium) rs1245917830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2141803 89751 RMVar_ID_89751 Human_SNP_ID_699302388 m1A Human chr22 - 21442822 21442822 21442822 AGTGCCAAGGGCCCAGACACCATGTGAGCAGCAGCCAGCGGCGGGGGGGGCTCCTGAGCGCGTGG AGTGCCAAGGGCCCAGACACCATGTGAGCAGCGGCCAGCGGCGGGGGGGGCTCCTGAGCGCGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:21442772..21442880;chr22:21442744..21442862 26863196 MeRIP-seq:(Medium) rs1419219097 Functional Loss SNV dbSNP153 33..33 33 - - - 89752 RMVar_ID_89752 Human_SNP_ID_699302394 m1A Human chr22 - 21442828 21442828 21442828 CACCGGAGTGCCAAGGGCCCAGACACCATGTGAGCAGCAGCCAGCGGCGGGGGGGGCTCCTGAGC CACCGGAGTGCCAAGGGCCCAGACACCATGTGGGCAGCAGCCAGCGGCGGGGGGGGCTCCTGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21442761..21442884 26863196 MeRIP-seq:(Medium) rs768231798 Functional Loss SNV dbSNP153 33..33 33 - - - 89753 RMVar_ID_89753 Human_SNP_ID_699303073 m1A Human chr22 + 21445217 21445217 21445217 TGGACTTCATCTACACAGGCAAGCTGCTGCCCAGCGACCAGCCAGCCGAGCCCAACTTCAGCACC TGGACTTCATCTACACAGGCAAGCTGCTGCCCGGCGACCAGCCAGCCGAGCCCAACTTCAGCACC A G HIC2 Ensembl:ENSG00000169635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21445137..21445250 26863196 MeRIP-seq:(Medium) rs749634954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18194020 RMVar_hsa_circ_213144,RMVar_hsa_circ_123871 89754 RMVar_ID_89754 Human_SNP_ID_699303486 m1A Human chr22 + 21446048 21446048 21446048 CCAATGGCATCCTGGCTAGTGGGGCTGGCCCTAGCGGGCCCTATGGGGAGCCCCCCTACCCCTGC CCAATGGCATCCTGGCTAGTGGGGCTGGCCCTGGCGGGCCCTATGGGGAGCCCCCCTACCCCTGC A G HIC2 Ensembl:ENSG00000169635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21446004..21446127 26863196 MeRIP-seq:(Medium) rs779002500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781584,Human_RBP_ID_929744,Human_RBP_ID_3962139,Human_RBP_ID_5529781,Human_RBP_ID_9300576,Human_RBP_ID_9333267,Human_RBP_ID_18194025,Human_RBP_ID_18423898,Human_RBP_ID_22086367,Human_RBP_ID_22454838,Human_RBP_ID_22604250,Human_RBP_ID_22723938,Human_RBP_ID_26345169,Human_RBP_ID_26770957 RMVar_hsa_circ_213144,RMVar_hsa_circ_123871 89755 RMVar_ID_89755 Human_SNP_ID_699309170 m1A Human chr22 - 21468271 21468271 21468271 GGTGTCAGGGGAGACAGGGACGGGGAGGCAACAAGGGCGAGGACAAGGGCAGGACTTCCGAGAGG GGTGTCAGGGGAGACAGGGACGGGGAGGCAACGAGGGCGAGGACAAGGGCAGGACTTCCGAGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21468265..21468348 26863196 MeRIP-seq:(Medium) rs1005459327 Functional Loss SNV dbSNP153 33..33 33 - - - 89756 RMVar_ID_89756 Human_SNP_ID_699325394 m1A Human chr22 - 21573600 21573599 21573600 GAAACCCTACTCGTGCTTAAAGGGCCAGGCCAAGTTCGACCTCCTCCTCAGTGTCAGAGGGGGTC GAAACCCTACTCGTGCTTAAAGGGCCAGGCCA_GTTCGACCTCCTCCTCAGTGTCAGAGGGGGTC CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:21573598..21573698 32194978 MeRIP-seq:(Medium) rs1337301772 Functional Loss DEL dbSNP153 33..33 33 - - - 89757 RMVar_ID_89757 Human_SNP_ID_699338167 m1A Human chr22 + 21621999 21621999 21621999 TTACATTTAACCCATAAGGTTTAAAAAAAAGGAAAAAAAACGGTTGTGGTTCCCTTTCTTCCCTA TTACATTTAACCCATAAGGTTTAAAAAAAAGGGAAAAAAACGGTTGTGGTTCCCTTTCTTCCCTA A G UBE2L3 Ensembl:ENSG00000185651 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200480773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575999,Human_RBP_ID_17286668,Human_RBP_ID_17514302,Human_RBP_ID_26496823 Human_miRNA_ID_2646482 RMVar_hsa_circ_94365,RMVar_hsa_circ_77446,RMVar_hsa_circ_213150,RMVar_hsa_circ_106718,RMVar_hsa_circ_213151,RMVar_hsa_circ_213153 89758 RMVar_ID_89758 Human_SNP_ID_699338298 m1A Human chr22 + 21622553 21622553 21622553 GAAGATCTGCTGGTCCTTGCAGGCAAAGCTACAGCCAGAATGTCCGTTTGAAACTCCTAGCTCAT GAAGATCTGCTGGTCCTTGCAGGCAAAGCTACGGCCAGAATGTCCGTTTGAAACTCCTAGCTCAT A G UBE2L3 Ensembl:ENSG00000185651 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:21622526..21622808 26863196 MeRIP-seq:(Medium) rs1029725276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281904,Human_RBP_ID_576018,Human_RBP_ID_14406755,Human_RBP_ID_22086377,Human_RBP_ID_23936760,Human_RBP_ID_26499961,Human_RBP_ID_26822274 Human_miRNA_ID_337308,Human_miRNA_ID_794836,Human_miRNA_ID_2333621,Human_miRNA_ID_2966705 RMVar_hsa_circ_94365,RMVar_hsa_circ_77446,RMVar_hsa_circ_213150,RMVar_hsa_circ_106718,RMVar_hsa_circ_213151,RMVar_hsa_circ_213153 89759 RMVar_ID_89759 Human_SNP_ID_699339844 m1A Human chr22 - 21628536 21628531 21628536 GCGCGTCCTCACCGCGCCCACGCTGCGGGCCCAGCTTGCCCAGGATGGCGTGCAGCTTTGCGCCC GCGCGTCCTCACCGCGCCCACGCTGCGGGCCC_____GCCCAGGATGGCGTGCAGCTTTGCGCCC CAAGCT C YDJC Ensembl:ENSG00000161179 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:21628445..21628538 26863410 MeRIP-seq:(Medium) rs775319690 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_576070,Human_RBP_ID_1608596,Human_RBP_ID_4687548,Human_RBP_ID_9124640,Human_RBP_ID_17989344,Human_RBP_ID_18194030 Human_miRNA_ID_1158791,Human_miRNA_ID_2041789,Human_miRNA_ID_3020766 RMVar_hsa_circ_87313,RMVar_hsa_circ_122365,RMVar_hsa_circ_79488,RMVar_hsa_circ_85961,RMVar_hsa_circ_213155,RMVar_hsa_circ_213156,RMVar_hsa_circ_213157,RMVar_hsa_circ_213154 89760 RMVar_ID_89760 Human_SNP_ID_699340477 m1A Human chr22 - 21629891 21629891 21629891 CCGGGGCTGTGACCAGCGTGTCCCTGCTGGTCAACGGTGCGGCCACGGAGAGCGCGGCGGAGCTG CCGGGGCTGTGACCAGCGTGTCCCTGCTGGTCCACGGTGCGGCCACGGAGAGCGCGGCGGAGCTG T G YDJC Ensembl:ENSG00000161179 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21629759..21630000 26863196 MeRIP-seq:(Medium) rs962625741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708073,Human_RBP_ID_5240793,Human_RBP_ID_5504357,Human_RBP_ID_9299696,Human_RBP_ID_9333274,Human_RBP_ID_17982686 Human_Splice_Rec_2142211,Human_Splice_Rec_2142215,Human_Splice_Rec_2142225,Human_Splice_Rec_2142233,Human_Splice_Rec_2142239,Human_Splice_Rec_2142245 Human_miRNA_ID_2027708,Human_miRNA_ID_2465316 RMVar_hsa_circ_122365,RMVar_hsa_circ_213157 89761 RMVar_ID_89761 Human_SNP_ID_699344311 m1A Human chr22 - 21642367 21642367 21642367 CAGCGCCAGCAGCAGCCCCAACAGCACCGGCCAGGCAGCCCCGCCGCGGCCCGCGCTCCACATCG CAGCGCCAGCAGCAGCCCCAACAGCACCGGCCGGGCAGCCCCGCCGCGGCCCGCGCTCCACATCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:21642256..21643082;chr22:21642276..21643075 26863196 MeRIP-seq:(Medium) rs985284043 Functional Loss SNV dbSNP153 33..33 33 - - - 89762 RMVar_ID_89762 Human_SNP_ID_699344312 m1A Human chr22 - 21642367 21642367 21642367 CAGCGCCAGCAGCAGCCCCAACAGCACCGGCCAGGCAGCCCCGCCGCGGCCCGCGCTCCACATCG CAGCGCCAGCAGCAGCCCCAACAGCACCGGCCCGGCAGCCCCGCCGCGGCCCGCGCTCCACATCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:21642256..21643082;chr22:21642276..21643075 26863196 MeRIP-seq:(Medium) rs985284043 Functional Loss SNV dbSNP153 33..33 33 - - - 89763 RMVar_ID_89763 Human_SNP_ID_699348913 m1A Human chr22 - 21657656 21657656 21657656 GGAGGCGGGGCCCGTCGTGCGGGACTGCCGGGACGCACCCTCTCTCCCCACGGCCGCGGCGCAGG GGAGGCGGGGCCCGTCGTGCGGGACTGCCGGGGCGCACCCTCTCTCCCCACGGCCGCGGCGCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21657619..21657724 26863196 MeRIP-seq:(Medium) rs1483779309 Functional Loss SNV dbSNP153 33..33 33 - - - 89764 RMVar_ID_89764 Human_SNP_ID_699351160 m1A Human chr22 + 21666100 21666100 21666100 TCGTGCTCGCTAGTCGCCGCCGCCGCTCCGCCATGGGGAAGCGACAGCACCAAAAGGACAAAATG TCGTGCTCGCTAGTCGCCGCCGCCGCTCCGCCGTGGGGAAGCGACAGCACCAAAAGGACAAAATG A G AP000553.1,PPIL2 Ensembl:ENSG00000207751,Ensembl:ENSG00000100023 lincRNA,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21666049..21666189 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_3962956,Human_RBP_ID_4708481,Human_RBP_ID_5250009,Human_RBP_ID_5324693,Human_RBP_ID_5601295,Human_RBP_ID_8263192,Human_RBP_ID_9332727,Human_RBP_ID_19007710,Human_RBP_ID_22086397,Human_RBP_ID_27821117 Human_Splice_Rec_2142289,Human_Splice_Rec_2142291,Human_Splice_Rec_2142331,Human_Splice_Rec_2142369,Human_Splice_Rec_2142409,Human_Splice_Rec_2142423,Human_Splice_Rec_2142465,Human_Splice_Rec_2142485,Human_Splice_Rec_2142525 89765 RMVar_ID_89765 Human_SNP_ID_699355413 m1A Human chr22 - 21680916 21680916 21680916 TCTCACCCACATCCTCCGCCAGCCCCCTGGTCAGCTCTTCCTTCAGAACCGCCCATCCCCTTGCC TCTCACCCACATCCTCCGCCAGCCCCCTGGTCCGCTCTTCCTTCAGAACCGCCCATCCCCTTGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21680908..21681103 26863196 MeRIP-seq:(Medium) rs1192210142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213161 89766 RMVar_ID_89766 Human_SNP_ID_699378481 m1A Human chr22 + 21764124 21764124 21764124 AAAGCCACAACTACCAGAAACCGCCCCTCCAAACGGCTCAAAGGAGTCAAAGTGGATAAGCCAAG AAAGCCACAACTACCAGAAACCGCCCCTCCAAGCGGCTCAAAGGAGTCAAAGTGGATAAGCCAAG A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:21764086..21769086 32194978 MeRIP-seq:(Medium) rs561937736 Functional Loss SNV dbSNP153 33..33 33 - - - 89767 RMVar_ID_89767 Human_SNP_ID_699389589 m1A Human chr22 - 21802367 21802363 21802368 AGGGTATCATAGGCAGAGAGTACAGAAATAAAATAAGAAGGAAGGGACTACTACCGAAAGCACTG AGGGTATCATAGGCAGAGAGTACAGAAATAA_____GAAGGAAGGGACTACTACCGAAAGCACTG CTTATT C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:21802361..21802472;chr22:21802364..21802498 26863196 MeRIP-seq:(Medium) rs201600790 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_2713052 RMVar_hsa_circ_29660,RMVar_hsa_circ_293631,RMVar_hsa_circ_213180,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_288512,RMVar_hsa_circ_306894,RMVar_hsa_circ_213181,RMVar_hsa_circ_213182,RMVar_hsa_circ_273250,RMVar_hsa_circ_213187 89768 RMVar_ID_89768 Human_SNP_ID_699401811 m1A Human chr22 + 21846897 21846897 21846897 TATTCCAATGATCTCAAAGTACCTACCCAAGCACAGTTCTAACTCTAGTATATGTAAGCAAACGT TATTCCAATGATCTCAAAGTACCTACCCAAGCGCAGTTCTAACTCTAGTATATGTAAGCAAACGT A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21846895..21846995 26863196 MeRIP-seq:(Medium) rs1241493673 Functional Loss SNV dbSNP153 33..33 33 - - - 89769 RMVar_ID_89769 Human_SNP_ID_699421654 m1A Human chr22 + 21921392 21921392 21921392 CTGCCTGGAGCAGCCCTGCCCACCTCCAGCTCAGCCCTTCCTGTGGCTTGGCCCTGCAGATGGCC CTGCCTGGAGCAGCCCTGCCCACCTCCAGCTCGGCCCTTCCTGTGGCTTGGCCCTGCAGATGGCC A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:21921341..21921461 26863196 MeRIP-seq:(Medium) rs1174560210 Functional Loss SNV dbSNP153 33..33 33 - - - 89770 RMVar_ID_89770 Human_SNP_ID_699421746 m1A Human chr22 + 21921861 21921861 21921861 AGGTCCCTCTGCCTGGGATCCAGCCAGGCCCAAGGGGGTGGGAATGCAGGCAGATGGGCCAAGGT AGGTCCCTCTGCCTGGGATCCAGCCAGGCCCAGGGGGGTGGGAATGCAGGCAGATGGGCCAAGGT A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:21921815..21922065 32194978 MeRIP-seq:(Medium) rs1206666177 Functional Loss SNV dbSNP153 33..33 33 - - - 89771 RMVar_ID_89771 Human_SNP_ID_699421881 m1A Human chr22 + 21922414 21922414 21922414 TTAGACCTCCCTGGAAAAAAACAAACACACCAACAAAAGACACATGTGCGTCGCCGGTTCCGGGC TTAGACCTCCCTGGAAAAAAACAAACACACCAGCAAAAGACACATGTGCGTCGCCGGTTCCGGGC A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:21922364..21922465 32194978 MeRIP-seq:(Medium) rs1253491948 Functional Loss SNV dbSNP153 33..33 33 - - - 89772 RMVar_ID_89772 Human_SNP_ID_699422144 m1A Human chr22 + 21923272 21923272 21923272 ATGTTGTCGTGGGAGCCCCGCTCCCGGGCCGCAGCCACCAGCTCCTCGGCGACACGGAGCCCGCT ATGTTGTCGTGGGAGCCCCGCTCCCGGGCCGCGGCCACCAGCTCCTCGGCGACACGGAGCCCGCT A G RF00017-049,RF00017-071 RNACentral:URS000096B6E3,RNACentral:URS00009310A4 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:21923222..21923375 26863196 MeRIP-seq:(Medium) rs1421674454 Functional Loss SNV dbSNP153 33..33 33 - - - 89773 RMVar_ID_89773 Human_SNP_ID_699426621 m1A Human chr22 - 21939645 21939645 21939645 GGCCCCGCCACCACTTGCTGCTGCTCTGGCCCACGAAGCAGTTTCACAGCTGCTACAGACAGACC GGCCCCGCCACCACTTGCTGCTGCTCTGGCCCGCGAAGCAGTTTCACAGCTGCTACAGACAGACC T C PPM1F Ensembl:ENSG00000100034 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21939594..21939713 26863196 MeRIP-seq:(Medium) rs745634939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962994,Human_RBP_ID_17982833,Human_RBP_ID_22086892 Human_Splice_Rec_2142628,Human_Splice_Rec_2142660,Human_Splice_Rec_2142670 Human_miRNA_ID_1354107,Human_miRNA_ID_2663877,Human_miRNA_ID_2682335 RMVar_hsa_circ_21394,RMVar_hsa_circ_31926 89774 RMVar_ID_89774 Human_SNP_ID_699428099 m1A Human chr22 - 21945941 21945941 21945941 CTCCTGCAAGACTTCCCAGCCCTGCTGAACCCAGAGGACCCTCTGCCATGGAAGGCCCCAGGGAC CTCCTGCAAGACTTCCCAGCCCTGCTGAACCCTGAGGACCCTCTGCCATGGAAGGCCCCAGGGAC T A PPM1F Ensembl:ENSG00000100034 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21945892..21946087 26863196 MeRIP-seq:(Medium) rs1358198059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576337,Human_RBP_ID_4708486,Human_RBP_ID_7065212,Human_RBP_ID_8865881,Human_RBP_ID_9300272 Human_Splice_Rec_2142627,Human_Splice_Rec_2142659 Human_miRNA_ID_936653,Human_miRNA_ID_2274232,Human_miRNA_ID_2425877,Human_miRNA_ID_2435547,Human_miRNA_ID_2571529,Human_miRNA_ID_3045265 89775 RMVar_ID_89775 Human_SNP_ID_699434967 m1A Human chr22 - 21970586 21970586 21970586 TGTTGTGGAGTGCTCAGGGCTTCTGGAAAGGCAGGGGGATAGAGGAGGGTCTGGCAGGTGCAGGA TGTTGTGGAGTGCTCAGGGCTTCTGGAAAGGCGGGGGGATAGAGGAGGGTCTGGCAGGTGCAGGA T C TOP3B Ensembl:ENSG00000100038 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21970584..21970694 26863196 MeRIP-seq:(Medium) rs1440388805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5324130 RMVar_hsa_circ_324949,RMVar_hsa_circ_213194,RMVar_hsa_circ_94779,RMVar_hsa_circ_213197,RMVar_hsa_circ_295017 89776 RMVar_ID_89776 Human_SNP_ID_699436274 m1A Human chr22 - 21975752 21975752 21975752 GTGCTGCGGAAGAGTGGAGTCTAAACTTTTTCATTGCCAGTGCCCCGAAACTGGAGTGTGAAGGA GTGCTGCGGAAGAGTGGAGTCTAAACTTTTTCGTTGCCAGTGCCCCGAAACTGGAGTGTGAAGGA T C TOP3B Ensembl:ENSG00000100038 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21975701..21975834 26863196 MeRIP-seq:(Medium) rs775516417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929312,Human_RBP_ID_1940271,Human_RBP_ID_4688118,Human_RBP_ID_8235679,Human_RBP_ID_14410809,Human_RBP_ID_18423702,Human_RBP_ID_18792605,Human_RBP_ID_22819754,Human_RBP_ID_23011203,Human_RBP_ID_23212891,Human_RBP_ID_26345204,Human_RBP_ID_26789492,Human_RBP_ID_27821136 Human_Splice_Rec_2142694,Human_Splice_Rec_2142748,Human_Splice_Rec_2142782,Human_Splice_Rec_2142816,Human_Splice_Rec_2142884,Human_Splice_Rec_2142894,Human_Splice_Rec_2142910,Human_Splice_Rec_2142916,Human_Splice_Rec_2142924,Human_Splice_Rec_2142928 RMVar_hsa_circ_324949,RMVar_hsa_circ_123672,RMVar_hsa_circ_213198,RMVar_hsa_circ_30850 89777 RMVar_ID_89777 Human_SNP_ID_699436819 m1A Human chr22 - 21977942 21977942 21977942 CTCCTTCTGCCTGGACTCTTCTCCCAGGTGTCACCCAGCCCTGCCCTGTCCCTCCCCTGCTCCCA CTCCTTCTGCCTGGACTCTTCTCCCAGGTGTCGCCCAGCCCTGCCCTGTCCCTCCCCTGCTCCCA T C TOP3B Ensembl:ENSG00000100038 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21977940..21978059 26863196 MeRIP-seq:(Medium) rs1485068022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132913,Human_RBP_ID_17087408,Human_RBP_ID_18952396 89778 RMVar_ID_89778 Human_SNP_ID_699437550 m1A Human chr22 + 21980716 21980716 21980716 AGCTGCATCTCCCAAGGCTCTGCTGCGCACCCACCTTTCCTCCCTGTGCGCCAGCAGGCTTCGGC AGCTGCATCTCCCAAGGCTCTGCTGCGCACCCGCCTTTCCTCCCTGTGCGCCAGCAGGCTTCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:21980714..21980782 26863196 MeRIP-seq:(Medium) rs1359920336 Functional Loss SNV dbSNP153 33..33 33 - - - 89779 RMVar_ID_89779 Human_SNP_ID_699437982 m1A Human chr22 + 21982652 21982652 21982652 CGAGCTCGCGGGTCCTCCGCCGGCCAACGTTCAGGAAACAAGCCAGAAAAATGCGTGCGCTTCCC CGAGCTCGCGGGTCCTCCGCCGGCCAACGTTCGGGAAACAAGCCAGAAAAATGCGTGCGCTTCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:21982650..21982800 26863196 MeRIP-seq:(Medium) rs889833757 Functional Loss SNV dbSNP153 33..33 33 - - - 89780 RMVar_ID_89780 Human_SNP_ID_699519457 m1A Human chr22 + 22285861 22285861 22285861 CACCTCATCTCATCATTTCATCTCGGCCTTTCATCTCTTCCTTTCATTTCATCTCATCGTTTCGT CACCTCATCTCATCATTTCATCTCGGCCTTTCGTCTCTTCCTTTCATTTCATCTCATCGTTTCGT A G lnc-IGLL5-1 RNACentral:URS00009BB799 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:22285174..22285923;chr22:22285276..22285925;chr22:22285124..22285923 26863196 MeRIP-seq:(Medium) rs550260311 Functional Loss SNV dbSNP153 33..33 33 - - - 89781 RMVar_ID_89781 Human_SNP_ID_699519838 m1A Human chr22 + 22286679 22286675 22286680 TCATCTCATCTCATCATTTCATCTCATCACTCATCTCATTTCATATCATCATTTTATCTCATCTC TCATCTCATCTCATCATTTCATCTCATCA_____CTCATTTCATATCATCATTTTATCTCATCTC ACTCAT A lnc-IGLL5-1 RNACentral:URS00009BB799 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22286367..22286771 26863196 MeRIP-seq:(Medium) rs1303941839 Functional Loss DEL dbSNP153 30..34 33 - - - 89782 RMVar_ID_89782 Human_SNP_ID_699520134 m1A Human chr22 - 22287189 22287189 22287189 GATGAGATGAGATGAAATGAGATGCAATAATGAGATGAAATGCGATAACGAGATGAGATGAGATG GATGAGATGAGATGAAATGAGATGCAATAATGGGATGAAATGCGATAACGAGATGAGATGAGATG T C AC245060.5 Ensembl:ENSG00000274422 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:22286944..22287276 26863196 MeRIP-seq:(Medium) rs201093883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10287,Human_RBP_ID_5653408,Human_RBP_ID_8235592,Human_RBP_ID_9444167,Human_RBP_ID_17659979,Human_RBP_ID_22525782,Human_RBP_ID_23285894,Human_RBP_ID_23937276,Human_RBP_ID_26345796 89783 RMVar_ID_89783 Human_SNP_ID_699523547 m1A Human chr22 - 22297926 22297926 22297926 TTGCGAGGGCGGAGCTGAGTTCTCCTTTGCACAGACTTCGGAGATACAGCGAAGGCAGAGCAATG TTGCGAGGGCGGAGCTGAGTTCTCCTTTGCACGGACTTCGGAGATACAGCGAAGGCAGAGCAATG T C lnc-ZNF280B-6 RNACentral:URS0000D5AEA8 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:22297879..22298007;chr22:22297878..22297989 26863196 MeRIP-seq:(Medium) rs1426041391 Functional Loss SNV dbSNP153 33..33 33 - - - 89784 RMVar_ID_89784 Human_SNP_ID_699525137 m1A Human chr22 + 22303126 22303126 22303126 GTGTTTCTAGTGATGGGAACAGTGAGAATCAGACTTGGAACACGGAGCGCATTGTGGGCCTGTCG GTGTTTCTAGTGATGGGAACAGTGAGAATCAGGCTTGGAACACGGAGCGCATTGTGGGCCTGTCG A G AC245060.7 Ensembl:ENSG00000286129 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22303107..22303205 26863196 MeRIP-seq:(Medium) rs199772824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14411332 89785 RMVar_ID_89785 Human_SNP_ID_699525346 m1A Human chr22 + 22303883 22303883 22303883 GATTTTTGTTTAAATAGAACTTTAAAAAATCTAATGTTTAAAGAAAAGACCTTCATAAACATACA GATTTTTGTTTAAATAGAACTTTAAAAAATCTGATGTTTAAAGAAAAGACCTTCATAAACATACA A G AC245060.4,AC245060.7 Ensembl:ENSG00000272779,Ensembl:ENSG00000286129 Pseudogene,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22303879..22304000 26863196 MeRIP-seq:(Medium) rs189195029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365036,RMVar_hsa_circ_354406 89786 RMVar_ID_89786 Human_SNP_ID_699526036 m1A Human chr22 + 22306758 22306758 22306758 CTGTCCACAGTTCCTTTACTTAGAAATTGCTCATTTGTTCATGTTAATGCTATGTTTATTACAGA CTGTCCACAGTTCCTTTACTTAGAAATTGCTCGTTTGTTCATGTTAATGCTATGTTTATTACAGA A G AC245060.4,AC245060.7 Ensembl:ENSG00000272779,Ensembl:ENSG00000286129 Pseudogene,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22306745..22306840 26863196 MeRIP-seq:(Medium) rs1433497839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17620731 RMVar_hsa_circ_7410,RMVar_hsa_circ_365036 89787 RMVar_ID_89787 Human_SNP_ID_699595040 m1A Human chr22 + 22547940 22547940 22547940 GAACATTTGTCTGAATGTTTTTTCCTCACTGAACATGTTTTCCTCACTCACACTGAACATTTGTC GAACATTTGTCTGAATGTTTTTTCCTCACTGATCATGTTTTCCTCACTCACACTGAACATTTGTC A T lnc-IGLL5-1,lnc-IGLL5-1:2,lnc-IGLL5-1:3,lnc-IGLL5-1:4,lnc-IGLL5-1:5,lnc-IGLL5-1:6,lnc-IGLL5-1:7,lnc-IGLL5-1:8,lnc-IGLL5-1:9,lnc-IGLL5-1:10,lnc-IGLL5-1:11,lnc-IGLL5-1:12,lnc-IGLL5-1:13,lnc-IGLL5-1:14,lnc-IGLL5-1:15,lnc-IGLL5-1:16,lnc-IGLL5-1:17,lnc-IGLL5-1:18,lnc-IGLL5-1:19,lnc-IGLL5-1:20,lnc-IGLL5-1:21 RNACentral:URS00009BBD2C,RNACentral:URS00009B8DBE,RNACentral:URS00009BB799,RNACentral:URS00009C12F8,RNACentral:URS00008C1359,RNACentral:URS00008C3338,RNACentral:URS00009C595C,RNACentral:URS00009B5BA5,RNACentral:URS00009B2118,RNACentral:URS00009C25C8,RNACentral:URS00009B5331,RNACentral:URS00009BE00F,RNACentral:URS00009BBB15,RNACentral:URS00009B6EB3,RNACentral:URS00009C0CA1,RNACentral:URS00009C4D42,RNACentral:URS00009B6AB5,RNACentral:URS00009C5A14,RNACentral:URS00009B7DD4,RNACentral:URS00009B056C,RNACentral:URS00009AFC13 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:22547833..22548051 26863196 MeRIP-seq:(Medium) rs1217437966 Functional Loss SNV dbSNP153 33..33 33 - - - 89788 RMVar_ID_89788 Human_SNP_ID_699599056 m1A Human chr22 - 22558911 22558911 22558911 TCTCTTCAGCCCGGGGGGTTACAGAAGTAGGTAAATCCAGAGATTACCCAGCCAAGGCCAGGGGC TCTCTTCAGCCCGGGGGGTTACAGAAGTAGGTGAATCCAGAGATTACCCAGCCAAGGCCAGGGGC T C PRAME Ensembl:ENSG00000185686 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:22558909..22558995 26863196 MeRIP-seq:(Medium) rs1179127687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676024,Human_RBP_ID_9433750,Human_RBP_ID_17087666,Human_RBP_ID_17572683 89789 RMVar_ID_89789 Human_SNP_ID_699599151 m1A Human chr22 + 22559145 22559145 22559145 GCAGAGGACTCCGCCCTGCTTTCCCTACATTCAGGGCTGCTCCTTTTGTCGCCAATACAGACCTG GCAGAGGACTCCGCCCTGCTTTCCCTACATTCTGGGCTGCTCCTTTTGTCGCCAATACAGACCTG A T lnc-IGLL5-1,lnc-IGLL5-1:2,lnc-IGLL5-1:3,lnc-IGLL5-1:4,lnc-IGLL5-1:5,lnc-IGLL5-1:6,lnc-IGLL5-1:7,lnc-IGLL5-1:8,lnc-IGLL5-1:9,lnc-IGLL5-1:10,lnc-IGLL5-1:11,lnc-IGLL5-1:12,lnc-IGLL5-1:13,lnc-IGLL5-1:14,lnc-IGLL5-1:15,lnc-IGLL5-1:16,lnc-IGLL5-1:17,lnc-IGLL5-1:18,lnc-IGLL5-1:19,lnc-IGLL5-1:20,lnc-IGLL5-1:21 RNACentral:URS00009BBD2C,RNACentral:URS00009B8DBE,RNACentral:URS00009BB799,RNACentral:URS00009C12F8,RNACentral:URS00008C1359,RNACentral:URS00008C3338,RNACentral:URS00009C595C,RNACentral:URS00009B5BA5,RNACentral:URS00009B2118,RNACentral:URS00009C25C8,RNACentral:URS00009B5331,RNACentral:URS00009BE00F,RNACentral:URS00009BBB15,RNACentral:URS00009B6EB3,RNACentral:URS00009C0CA1,RNACentral:URS00009C4D42,RNACentral:URS00009B6AB5,RNACentral:URS00009C5A14,RNACentral:URS00009B7DD4,RNACentral:URS00009B056C,RNACentral:URS00009AFC13 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22559097..22559180 26863196 MeRIP-seq:(Medium) rs929216602 Functional Loss SNV dbSNP153 33..33 33 - - - 89790 RMVar_ID_89790 Human_SNP_ID_699741703 m1A Human chr22 - 23070454 23070454 23070454 CCTCGTTCCGTACGACGCGGGCAGCGGCGCCCACGCGGGGACGTGACCGGACCGCGGGCGGCGCA CCTCGTTCCGTACGACGCGGGCAGCGGCGCCCTCGCGGGGACGTGACCGGACCGCGGGCGGCGCA T A RSPH14 Ensembl:ENSG00000100218 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:23070404..23070499 26863196 MeRIP-seq:(Medium) rs1204619582 Functional Loss SNV dbSNP153 33..33 33 - - - 89791 RMVar_ID_89791 Human_SNP_ID_699747836 m1A Human chr22 + 23095318 23095318 23095318 GCTGCAGGGAGCACACCAGCGACCGGCCCTCCAACCCTCCAGCCACTCAGCAACATCGCCACAGC GCTGCAGGGAGCACACCAGCGACCGGCCCTCCCACCCTCCAGCCACTCAGCAACATCGCCACAGC A C GNAZ Ensembl:ENSG00000128266 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23095268..23095394 26863196 MeRIP-seq:(Medium) rs988734075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708860 Human_Splice_Rec_2143338,Human_Splice_Rec_2143342 Human_miRNA_ID_2294623 RMVar_hsa_circ_213236,RMVar_hsa_circ_299519 89792 RMVar_ID_89792 Human_SNP_ID_699769791 m1A Human chr22 + 23180570 23180570 23180570 GAGAGCCGGCTGGCTGAGCTTAGCGTCCGAGGAGGCGGCGGCGGCGGCGGCGGCACGGCGGCGGC GAGAGCCGGCTGGCTGAGCTTAGCGTCCGAGGCGGCGGCGGCGGCGGCGGCGGCACGGCGGCGGC A C BCR Ensembl:ENSG00000186716 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:23180521..23181340;chr22:23180526..23180817 26863196 MeRIP-seq:(Medium) rs1298370504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153454,Human_RBP_ID_3962210,Human_RBP_ID_9332740,Human_RBP_ID_22533820,Human_RBP_ID_24553754 RMVar_hsa_circ_266517 89793 RMVar_ID_89793 Human_SNP_ID_699769895 m1A Human chr22 + 23180679 23180679 23180679 GCCGTGGCCAGAGTCTGGCGGCGGCCTGGCGGAGCGGAGAGCAGCGCCCGCGCCTCGCCGTGCGG GCCGTGGCCAGAGTCTGGCGGCGGCCTGGCGGGGCGGAGAGCAGCGCCCGCGCCTCGCCGTGCGG A G BCR Ensembl:ENSG00000186716 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:23180598..23180800 26863410 MeRIP-seq:(Medium) rs1241577345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153454,Human_RBP_ID_3962211,Human_RBP_ID_4688385,Human_RBP_ID_5148973,Human_RBP_ID_5472881 RMVar_hsa_circ_266517 89794 RMVar_ID_89794 Human_SNP_ID_699769923 m1A Human chr22 + 23180725 23180725 23180725 CCCGCGCCTCGCCGTGCGGAGGAGCCCCGCACACAATAGCGGCGCGCGCAGCCCGCGCCCTTCCC CCCGCGCCTCGCCGTGCGGAGGAGCCCCGCACCCAATAGCGGCGCGCGCAGCCCGCGCCCTTCCC A C BCR Ensembl:ENSG00000186716 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:23180629..23180780 32194978 MeRIP-seq:(Medium) rs1160570806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266517 89795 RMVar_ID_89795 Human_SNP_ID_699770098 m1A Human chr22 - 23180974 23180974 23180974 GGAACTGCGCCTTCCACGCCTCCGCGAAGCCCACCGGGTCCACCATGGCGCGGCCGGCCTTACCT GGAACTGCGCCTTCCACGCCTCCGCGAAGCCCTCCGGGTCCACCATGGCGCGGCCGGCCTTACCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23180925..23181515 26863196 MeRIP-seq:(Medium) rs1408782317 Functional Loss SNV dbSNP153 33..33 33 - - - 89796 RMVar_ID_89796 Human_SNP_ID_699770719 m1A Human chr22 + 23181952 23181952 23181952 TTTTGAGGATTGCGGAGGCGGCTATACCCCGGACTGCAGCTCCAATGAGAACCTCACCTCCAGCG TTTTGAGGATTGCGGAGGCGGCTATACCCCGGGCTGCAGCTCCAATGAGAACCTCACCTCCAGCG A G BCR Ensembl:ENSG00000186716 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:23181901..23181975 26863196 MeRIP-seq:(Medium) rs1193632023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929756,Human_RBP_ID_3963033,Human_RBP_ID_8861704,Human_RBP_ID_9260663,Human_RBP_ID_9300293,Human_RBP_ID_14412031,Human_RBP_ID_18194049,Human_RBP_ID_22086456,Human_RBP_ID_24553755,Human_RBP_ID_27492223,Human_RBP_ID_27565173 RMVar_hsa_circ_266517 89797 RMVar_ID_89797 Human_SNP_ID_699782231 m1A Human chr22 - 23222480 23222480 23222480 GAACCACTTCCCCTGCTCTGAACTTTCTCAGCACTTAGCACTTGTGCAATTTATCTGACAATCGT GAACCACTTCCCCTGCTCTGAACTTTCTCAGCGCTTAGCACTTGTGCAATTTATCTGACAATCGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:23222478..23222612 26863196 MeRIP-seq:(Medium) rs1324519436 Functional Loss SNV dbSNP153 33..33 33 - - - 89798 RMVar_ID_89798 Human_SNP_ID_699785317 m1A Human chr22 + 23234484 23234484 23234484 ATGAGAAGTTTTGAGGGGACTGGTGCCTGGACATGGGCTGTAGCGTAGGTGGAGTGTCGAGGAGG ATGAGAAGTTTTGAGGGGACTGGTGCCTGGACGTGGGCTGTAGCGTAGGTGGAGTGTCGAGGAGG A G BCR Ensembl:ENSG00000186716 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23234481..23234736 26863196 MeRIP-seq:(Medium) rs913453988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107567,RMVar_hsa_circ_266517,RMVar_hsa_circ_213245,RMVar_hsa_circ_80742,RMVar_hsa_circ_213244 89799 RMVar_ID_89799 Human_SNP_ID_699796350 m1A Human chr22 + 23273683 23273683 23273683 TCCTGCCAGCCACCCTGACCACCCCTTGCTGCAGGACGCCCTCCGCATCTCACAGAACTTCCTGT TCCTGCCAGCCACCCTGACCACCCCTTGCTGCCGGACGCCCTCCGCATCTCACAGAACTTCCTGT A C BCR Ensembl:ENSG00000186716 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:23273656..23273785 26863196 MeRIP-seq:(Medium) rs1290431418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962227,Human_RBP_ID_8861716,Human_RBP_ID_9300305 Human_Splice_Rec_2143410,Human_Splice_Rec_2143411,Human_Splice_Rec_2143452,Human_Splice_Rec_2143453,Human_Splice_Rec_2143504,Human_Splice_Rec_2143505 RMVar_hsa_circ_1308,RMVar_hsa_circ_107567,RMVar_hsa_circ_266517,RMVar_hsa_circ_96384,RMVar_hsa_circ_28068,RMVar_hsa_circ_213245,RMVar_hsa_circ_80742,RMVar_hsa_circ_213244,RMVar_hsa_circ_315544,RMVar_hsa_circ_1625,RMVar_hsa_circ_213246,RMVar_hsa_circ_110959,RMVar_hsa_circ_213248,RMVar_hsa_circ_213249,RMVar_hsa_circ_213250,RMVar_hsa_circ_287122,RMVar_hsa_circ_368505,RMVar_hsa_circ_310913,RMVar_hsa_circ_346879,RMVar_hsa_circ_213253,RMVar_hsa_circ_95732,RMVar_hsa_circ_101659,RMVar_hsa_circ_117852,RMVar_hsa_circ_280132,RMVar_hsa_circ_213251,RMVar_hsa_circ_120679,RMVar_hsa_circ_113298,RMVar_hsa_circ_100209,RMVar_hsa_circ_213257,RMVar_hsa_circ_85510,RMVar_hsa_circ_89422,RMVar_hsa_circ_213259,RMVar_hsa_circ_213261,RMVar_hsa_circ_78984,RMVar_hsa_circ_213260,RMVar_hsa_circ_213258,RMVar_hsa_circ_213255,RMVar_hsa_circ_213256,RMVar_hsa_circ_213254,RMVar_hsa_circ_97297,RMVar_hsa_circ_213252,RMVar_hsa_circ_213262 89800 RMVar_ID_89800 Human_SNP_ID_699808150 m1A Human chr22 + 23313992 23313992 23313992 TTCTGCAGCTCTTTCAGACCCGGTTGCAAAGGAGAGCTGCATGCTCAACCTGCTGCTGTCCCTGC TTCTGCAGCTCTTTCAGACCCGGTTGCAAAGGCGAGCTGCATGCTCAACCTGCTGCTGTCCCTGC A C BCR Ensembl:ENSG00000186716 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:23312997..23314572 32194978 MeRIP-seq:(Medium) rs1198893680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2143434,Human_Splice_Rec_2143435,Human_Splice_Rec_2143478,Human_Splice_Rec_2143479,Human_Splice_Rec_2143546,Human_Splice_Rec_2143550,Human_Splice_Rec_2143551 Human_miRNA_ID_1241385,Human_miRNA_ID_1457179,Human_miRNA_ID_2598542,Human_miRNA_ID_3042030 RMVar_hsa_circ_100209,RMVar_hsa_circ_213252,RMVar_hsa_circ_91311,RMVar_hsa_circ_213264,RMVar_hsa_circ_84683,RMVar_hsa_circ_213265,RMVar_hsa_circ_76530,RMVar_hsa_circ_213267,RMVar_hsa_circ_335294 89801 RMVar_ID_89801 Human_SNP_ID_699895069 m1A Human chr22 - 23641445 23641444 23641445 AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGAAGTGATTAGTTTGAGACTCCTGTTGGGTAGCCC AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGA_GTGATTAGTTTGAGACTCCTGTTGGGTAGCCC CT C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23641395..23641532 26863196 MeRIP-seq:(Medium) rs546348540 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14412865,Human_RBP_ID_22604335 89802 RMVar_ID_89802 Human_SNP_ID_699895072 m1A Human chr22 - 23641445 23641445 23641445 AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGAAGTGATTAGTTTGAGACTCCTGTTGGGTAGCCC AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGATGTGATTAGTTTGAGACTCCTGTTGGGTAGCCC T A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23641395..23641532 26863196 MeRIP-seq:(Medium) rs201501506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14412865,Human_RBP_ID_22604335 89803 RMVar_ID_89803 Human_SNP_ID_699895073 m1A Human chr22 - 23641445 23641445 23641445 AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGAAGTGATTAGTTTGAGACTCCTGTTGGGTAGCCC AGTTGGGCTGGGGGAAGGTGGTCATCTCTGGACGTGATTAGTTTGAGACTCCTGTTGGGTAGCCC T G GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23641395..23641532 26863196 MeRIP-seq:(Medium) rs201501506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14412865,Human_RBP_ID_22604335 89804 RMVar_ID_89804 Human_SNP_ID_699895966 m1A Human chr22 - 23644671 23644671 23644671 TGGTGGTGAAGGTTGCCCAACAGTGTGAATGTACTTAGTGCCACGGAGCTGTACTTTTAAAAATA TGGTGGTGAAGGTTGCCCAACAGTGTGAATGTCCTTAGTGCCACGGAGCTGTACTTTTAAAAATA T G GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23644662..23644746 26863196 MeRIP-seq:(Medium) rs1302495523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23937612 89805 RMVar_ID_89805 Human_SNP_ID_699899288 m1A Human chr22 + 23656994 23656994 23656994 GCATGAGCCACTGCACCCAGCCCGCCTGGCCCATTTTGTTTTTCTTTTCTTTTCTTTTTTTTTGA GCATGAGCCACTGCACCCAGCCCGCCTGGCCCCTTTTGTTTTTCTTTTCTTTTCTTTTTTTTTGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23656949..23657015 26863196 MeRIP-seq:(Medium) rs1240437255 Functional Loss SNV dbSNP153 33..33 33 - - - 89806 RMVar_ID_89806 Human_SNP_ID_699899289 m1A Human chr22 + 23656994 23656994 23656994 GCATGAGCCACTGCACCCAGCCCGCCTGGCCCATTTTGTTTTTCTTTTCTTTTCTTTTTTTTTGA GCATGAGCCACTGCACCCAGCCCGCCTGGCCCTTTTTGTTTTTCTTTTCTTTTCTTTTTTTTTGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23656949..23657015 26863196 MeRIP-seq:(Medium) rs1240437255 Functional Loss SNV dbSNP153 33..33 33 - - - 89807 RMVar_ID_89807 Human_SNP_ID_699899547 m1A Human chr22 - 23657762 23657752 23657762 GAGGAGGAGGAGGAAAAAGAAATGGAGGAGGAAAAAGAAACAGGAGGAGGAAAAAGAAACGGAGG GAGGAGGAGGAGGAAAAAGAAATGGAGGAGGA__________GGAGGAGGAAAAAGAAACGGAGG CTGTTTCTTTT C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23657592..23658161 26863196 MeRIP-seq:(Medium) rs879264686 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_1614365,Human_RBP_ID_3679468,Human_RBP_ID_5101559,Human_RBP_ID_17069198,Human_RBP_ID_23015572 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 89808 RMVar_ID_89808 Human_SNP_ID_699899568 m1A Human chr22 - 23657769 23657766 23657770 AATGGAGGAGGAGGAGGAGGAAAAAGAAATGGAGGAGGAAAAAGAAACAGGAGGAGGAAAAAGAA AATGGAGGAGGAGGAGGAGGAAAAAGAAATG____AGGAAAAAGAAACAGGAGGAGGAAAAAGAA TCCTC T GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23657645..23657861 26863196 MeRIP-seq:(Medium) rs1474122119 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_1614365,Human_RBP_ID_3679468,Human_RBP_ID_4688524,Human_RBP_ID_5101559,Human_RBP_ID_17069198,Human_RBP_ID_23015572 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 89809 RMVar_ID_89809 Human_SNP_ID_699899576 m1A Human chr22 - 23657769 23657769 23657769 AATGGAGGAGGAGGAGGAGGAAAAAGAAATGGAGGAGGAAAAAGAAACAGGAGGAGGAAAAAGAA AATGGAGGAGGAGGAGGAGGAAAAAGAAATGGTGGAGGAAAAAGAAACAGGAGGAGGAAAAAGAA T A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23657645..23657861 26863196 MeRIP-seq:(Medium) rs1486680641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1614365,Human_RBP_ID_3679468,Human_RBP_ID_4688524,Human_RBP_ID_5101559,Human_RBP_ID_17069198,Human_RBP_ID_23015572 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 89810 RMVar_ID_89810 Human_SNP_ID_699904909 m1A Human chr22 - 23677952 23677952 23677952 TGGGAGCAGCTGGACAGGCCCAGTGAGGATGCAGGGGCAGCTGCCCAGGGCTAGACTCTGGCTGC TGGGAGCAGCTGGACAGGCCCAGTGAGGATGCGGGGGCAGCTGCCCAGGGCTAGACTCTGGCTGC T C GUSBP11,AP000347.1 Ensembl:ENSG00000228315,Ensembl:ENSG00000272578 lincRNA,Pseudogene intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:23677949..23678056 26863196 MeRIP-seq:(Medium) rs73157081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5599646,Human_RBP_ID_18516519 RMVar_hsa_circ_39823,RMVar_hsa_circ_213273,RMVar_hsa_circ_93202,RMVar_hsa_circ_347237,RMVar_hsa_circ_369337,RMVar_hsa_circ_278348,RMVar_hsa_circ_213274,RMVar_hsa_circ_213275 89811 RMVar_ID_89811 Human_SNP_ID_699907092 m1A Human chr22 - 23686971 23686971 23686971 AATCACAGAAAATAAAGCATGCGAAGAAGTTAACTTGGTGCCATTGGGCAGAGGGTGAGAGCCCA AATCACAGAAAATAAAGCATGCGAAGAAGTTACCTTGGTGCCATTGGGCAGAGGGTGAGAGCCCA T G GUSBP11,AP000347.1 Ensembl:ENSG00000228315,Ensembl:ENSG00000272578 lincRNA,Pseudogene exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:23686920..23687025 26863196 MeRIP-seq:(Medium) rs913996533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3678920,Human_RBP_ID_5101206,Human_RBP_ID_14413561,Human_RBP_ID_18535286,Human_RBP_ID_24381044 Human_Splice_Rec_2143852,Human_Splice_Rec_2143874,Human_Splice_Rec_2143900,Human_Splice_Rec_2143906,Human_Splice_Rec_2143908 RMVar_hsa_circ_39823,RMVar_hsa_circ_213273,RMVar_hsa_circ_93202,RMVar_hsa_circ_347237,RMVar_hsa_circ_369337,RMVar_hsa_circ_213276,RMVar_hsa_circ_278737,RMVar_hsa_circ_213275,RMVar_hsa_circ_337871,RMVar_hsa_circ_361933,RMVar_hsa_circ_43344,RMVar_hsa_circ_52570,RMVar_hsa_circ_213277 89812 RMVar_ID_89812 Human_SNP_ID_699929372 m1A Human chr22 - 23765941 23765941 23765941 ACCCACCTCTACCCCTCGCCGACAGCCAGACCACAACACCAGATTGTACCCAGATAGCTGGGATT ACCCACCTCTACCCCTCGCCGACAGCCAGACCGCAACACCAGATTGTACCCAGATAGCTGGGATT T C CHCHD10 Ensembl:ENSG00000250479 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23765891..23765960 26863196 MeRIP-seq:(Medium) rs1000462749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576515,Human_RBP_ID_1028566,Human_RBP_ID_17287177,Human_RBP_ID_17660207 Human_Splice_Rec_2144150,Human_Splice_Rec_2144156,Human_Splice_Rec_2144162,Human_Splice_Rec_2144164,Human_Splice_Rec_2144170 RMVar_hsa_circ_95843,RMVar_hsa_circ_106045,RMVar_hsa_circ_213286,RMVar_hsa_circ_213288,RMVar_hsa_circ_86891,RMVar_hsa_circ_213287 89813 RMVar_ID_89813 Human_SNP_ID_699929437 m1A Human chr22 - 23766058 23766058 23766058 GAGGCCAACCCTCCTCTTGCACCTGCAGGCTGACCACCAGCCTGTGCTGCCCCTCCCTTCCCAGG GAGGCCAACCCTCCTCTTGCACCTGCAGGCTGCCCACCAGCCTGTGCTGCCCCTCCCTTCCCAGG T G CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23766054..23766135 26863196 MeRIP-seq:(Medium) rs777266617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929762,Human_RBP_ID_19112841 RMVar_hsa_circ_95843,RMVar_hsa_circ_106045,RMVar_hsa_circ_213286,RMVar_hsa_circ_213287 89814 RMVar_ID_89814 Human_SNP_ID_699929566 m1A Human chr22 - 23766269 23766269 23766269 TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCACCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCGCCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG T C CHCHD10 Ensembl:ENSG00000250479 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs767301039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2144148,Human_Splice_Rec_2144154,Human_Splice_Rec_2144160,Human_Splice_Rec_2144168 Human_miRNA_ID_1359320,Human_miRNA_ID_2686590 RMVar_hsa_circ_95843,RMVar_hsa_circ_106045,RMVar_hsa_circ_213286,RMVar_hsa_circ_213287 89815 RMVar_ID_89815 Human_SNP_ID_699929567 m1A Human chr22 - 23766269 23766269 23766269 TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCACCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCCCCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG T G CHCHD10 Ensembl:ENSG00000250479 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs767301039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2144148,Human_Splice_Rec_2144154,Human_Splice_Rec_2144160,Human_Splice_Rec_2144168 Human_miRNA_ID_1359320,Human_miRNA_ID_2686590 RMVar_hsa_circ_95843,RMVar_hsa_circ_106045,RMVar_hsa_circ_213286,RMVar_hsa_circ_213287 89816 RMVar_ID_89816 Human_SNP_ID_699929936 m1A Human chr22 - 23767476 23767476 23767476 GGGCTCATGGCTCAGATGGCGACCACGGCCGCAGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT GGGCTCATGGCTCAGATGGCGACCACGGCCGCGGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT T C CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:23767426..23767660 26863196 MeRIP-seq:(Medium) rs748608906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576527,Human_RBP_ID_1028568,Human_RBP_ID_4708092,Human_RBP_ID_22454580 Human_Splice_Rec_2144166 Human_miRNA_ID_2937811 RMVar_hsa_circ_106045,RMVar_hsa_circ_213286 89817 RMVar_ID_89817 Human_SNP_ID_699929937 m1A Human chr22 - 23767476 23767476 23767476 GGGCTCATGGCTCAGATGGCGACCACGGCCGCAGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT GGGCTCATGGCTCAGATGGCGACCACGGCCGCCGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT T G CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:23767426..23767660 26863196 MeRIP-seq:(Medium) rs748608906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576527,Human_RBP_ID_1028568,Human_RBP_ID_4708092,Human_RBP_ID_22454580 Human_Splice_Rec_2144166 Human_miRNA_ID_2937811 RMVar_hsa_circ_106045,RMVar_hsa_circ_213286 89818 RMVar_ID_89818 Human_SNP_ID_699930001 m1A Human chr22 - 23767587 23767587 23767587 AACCCTGCTTCCTCCCACCCCCGCAGCCGCCCAGCCGCGCCCTCTGCCCACCCGCCCGCGCACCC AACCCTGCTTCCTCCCACCCCCGCAGCCGCCCCGCCGCGCCCTCTGCCCACCCGCCCGCGCACCC T G CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:23767571..23767909 32194978 MeRIP-seq:(Medium) rs179468 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_781822,Human_RBP_ID_22533826 Human_Splice_Rec_2144152,Human_Splice_Rec_2144158 Human_miRNA_ID_2274244,Human_miRNA_ID_2874402,Human_miRNA_ID_2982362 GWAS_ID_11654,GWAS_ID_11655,GWAS_ID_11656,GWAS_ID_11657,GWAS_ID_11658 RMVar_hsa_circ_106045,RMVar_hsa_circ_213286 89819 RMVar_ID_89819 Human_SNP_ID_699930079 m1A Human chr22 + 23767788 23767788 23767788 GTCACTCTGCGGACGCCCTTAGGGGAGTGCCCACACTTCCCTAACCCCCTCCCCACAGGGCCCTT GTCACTCTGCGGACGCCCTTAGGGGAGTGCCCCCACTTCCCTAACCCCCTCCCCACAGGGCCCTT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:23767780..23767950 26863196 MeRIP-seq:(Medium) rs62241575 Functional Loss SNV dbSNP153 33..33 33 - - - 89820 RMVar_ID_89820 Human_SNP_ID_699947354 m1A Human chr22 + 23829200 23829200 23829200 GGGAGGAGACAGTGCCCTGTCTGGCAGAGGAAACAGATTCATGTGCATGACTATCAGTGTGCCAT GGGAGGAGACAGTGCCCTGTCTGGCAGAGGAAGCAGATTCATGTGCATGACTATCAGTGTGCCAT A G SMARCB1 Ensembl:ENSG00000099956 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:23829198..23829437 26863196 MeRIP-seq:(Medium) rs1363094499 Functional Loss SNV dbSNP153 33..33 33 - - - 89821 RMVar_ID_89821 Human_SNP_ID_699950172 m1A Human chr22 + 23838580 23838577 23838580 GCAGGGCGCAGGATACACGAAGAGCATGTTGAAGAAGAAGCTGAATCCCAGGGGCCCGAAGAAGA GCAGGGCGCAGGATACACGAAGAGCATGTT___GAAGAAGCTGAATCCCAGGGGCCCGAAGAAGA TGAA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23838573..23838677 26863196 MeRIP-seq:(Medium) rs759080001 Functional Loss DEL dbSNP153 31..33 33 - - - 89822 RMVar_ID_89822 Human_SNP_ID_699950394 m1A Human chr22 + 23838960 23838960 23838960 GTAAGCCCGCGTCACCGCCGGCACCTGCAGGAACTCGGCCGCTAGTCCCTGCCACGCCATTGAAC GTAAGCCCGCGTCACCGCCGGCACCTGCAGGACCTCGGCCGCTAGTCCCTGCCACGCCATTGAAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23838847..23838975 26863196 MeRIP-seq:(Medium) rs562126764 Functional Loss SNV dbSNP153 33..33 33 - - - 89823 RMVar_ID_89823 Human_SNP_ID_699955876 m1A Human chr22 - 23857957 23857957 23857957 GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGACCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGGCCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23857911..23858002 26863196 MeRIP-seq:(Medium) rs778744344 Functional Loss SNV dbSNP153 33..33 33 - - - 89824 RMVar_ID_89824 Human_SNP_ID_699955877 m1A Human chr22 - 23857957 23857957 23857957 GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGACCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGCCCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23857911..23858002 26863196 MeRIP-seq:(Medium) rs778744344 Functional Loss SNV dbSNP153 33..33 33 - - - 89825 RMVar_ID_89825 Human_SNP_ID_699960997 m1A Human chr22 + 23877166 23877166 23877166 GCTCTGGGGATCGTGATGGGACAGGTGGTCGGACTCAGGTAAGCACCCCTCCCCCACATGCATTG GCTCTGGGGATCGTGATGGGACAGGTGGTCGGGCTCAGGTAAGCACCCCTCCCCCACATGCATTG A G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23877116..23877217 26863196 MeRIP-seq:(Medium) rs747417327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834026 Human_Splice_Rec_2144515,Human_Splice_Rec_2144545,Human_Splice_Rec_2144577,Human_Splice_Rec_2144593,Human_Splice_Rec_2144605,Human_Splice_Rec_2144625,Human_Splice_Rec_2144653,Human_Splice_Rec_2144703,Human_Splice_Rec_2144725,Human_Splice_Rec_2144741,Human_Splice_Rec_2144757,Human_Splice_Rec_2144781 RMVar_hsa_circ_91528,RMVar_hsa_circ_122275,RMVar_hsa_circ_213297,RMVar_hsa_circ_213298 89826 RMVar_ID_89826 Human_SNP_ID_699962335 m1A Human chr22 + 23881953 23881951 23881953 GATTGAGAGAGACAGAGGCAGAGAGAGAGAGAAACACACACACACACACACACACAGAGACAGAG GATTGAGAGAGACAGAGGCAGAGAGAGAGAG__ACACACACACACACACACACACAGAGACAGAG GAA G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23881945..23882121 26863196 MeRIP-seq:(Medium) rs1241810704 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23011370 89827 RMVar_ID_89827 Human_SNP_ID_699962347 m1A Human chr22 + 23881953 23881953 23881953 GATTGAGAGAGACAGAGGCAGAGAGAGAGAGAAACACACACACACACACACACACAGAGACAGAG GATTGAGAGAGACAGAGGCAGAGAGAGAGAGACACACACACACACACACACACACAGAGACAGAG A C AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23881945..23882121 26863196 MeRIP-seq:(Medium) rs1194954241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23011370 89828 RMVar_ID_89828 Human_SNP_ID_699962348 m1A Human chr22 + 23881953 23881953 23881953 GATTGAGAGAGACAGAGGCAGAGAGAGAGAGAAACACACACACACACACACACACAGAGACAGAG GATTGAGAGAGACAGAGGCAGAGAGAGAGAGAGACACACACACACACACACACACAGAGACAGAG A G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23881945..23882121 26863196 MeRIP-seq:(Medium) rs1194954241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23011370 89829 RMVar_ID_89829 Human_SNP_ID_699962512 m1A Human chr22 + 23882214 23882207 23882215 GCAGAGAGAGAGAGAAACACACACACACACACAGACACAGAGACAGAGAGATTGAGAGGCAGAGA GCAGAGAGAGAGAGAAACACACACAC________ACACAGAGACAGAGAGATTGAGAGGCAGAGA CACACACAG C AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23882208..23882920 26863196 MeRIP-seq:(Medium) rs1401182326 Functional Loss DEL dbSNP153 27..34 33 - - - 89830 RMVar_ID_89830 Human_SNP_ID_699965859 m1A Human chr22 + 23894401 23894401 23894401 AAAGGCGGGACCACAGTGGTGTCCGAGAAGTCAGGCACGTAGCTCAGCGGCGGCCGCGGCGCGTG AAAGGCGGGACCACAGTGGTGTCCGAGAAGTCTGGCACGTAGCTCAGCGGCGGCCGCGGCGCGTG A T AP000350.4,MIF Ensembl:ENSG00000251357,Ensembl:ENSG00000240972 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:23894376..23894400 26863196 MeRIP-seq:(Medium) rs112568463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576610,Human_RBP_ID_1028582,Human_RBP_ID_1200954,Human_RBP_ID_4688741,Human_RBP_ID_5202934,Human_RBP_ID_7066076,Human_RBP_ID_8861749,Human_RBP_ID_22455165,Human_RBP_ID_22819817,Human_RBP_ID_23134276,Human_RBP_ID_23937869,Human_RBP_ID_26501364,Human_RBP_ID_27033703,Human_RBP_ID_27492281 RMVar_hsa_circ_78844,RMVar_hsa_circ_213300 89831 RMVar_ID_89831 Human_SNP_ID_699965931 m1A Human chr22 + 23894499 23894499 23894499 CTGCCATCATGCCGATGTTCATCGTAAACACCAACGTGCCCCGCGCCTCCGTGCCGGACGGGTTC CTGCCATCATGCCGATGTTCATCGTAAACACCGACGTGCCCCGCGCCTCCGTGCCGGACGGGTTC A G AP000350.4,MIF Ensembl:ENSG00000251357,Ensembl:ENSG00000240972 Protein coding,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:23894399..23894803 26863196 MeRIP-seq:(Medium) rs777547459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65766,Human_RBP_ID_576612,Human_RBP_ID_1608917,Human_RBP_ID_1940438,Human_RBP_ID_3669367,Human_RBP_ID_4688745,Human_RBP_ID_5324147,Human_RBP_ID_5424302,Human_RBP_ID_5446322,Human_RBP_ID_5472894,Human_RBP_ID_5504407,Human_RBP_ID_8262286,Human_RBP_ID_9332768,Human_RBP_ID_17660213,Human_RBP_ID_17983051,Human_RBP_ID_18194061,Human_RBP_ID_18785649,Human_RBP_ID_22454852,Human_RBP_ID_22507686,Human_RBP_ID_26501365,Human_RBP_ID_26822313,Human_RBP_ID_27305503 Human_Splice_Rec_2144785,Human_Splice_Rec_2144789 Human_miRNA_ID_2250441,Human_miRNA_ID_3066507 RMVar_hsa_circ_78844,RMVar_hsa_circ_213300 89832 RMVar_ID_89832 Human_SNP_ID_699965941 m1A Human chr22 - 23894514 23894514 23894514 GGTGAGCTCGGAGAGGAACCCGTCCGGCACGGAGGCGCGGGGCACGTTGGTGTTTACGATGAACA GGTGAGCTCGGAGAGGAACCCGTCCGGCACGGCGGCGCGGGGCACGTTGGTGTTTACGATGAACA T G MIF-AS1 Ensembl:ENSG00000218537 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr22:23894405..23894579 26863410 MeRIP-seq:(Medium) rs1187914662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5600507 89833 RMVar_ID_89833 Human_SNP_ID_699965970 m1A Human chr22 + 23894572 23894572 23894572 GCTCACCCAGCAGCTGGCGCAGGCCACCGGCAAGCCCCCCCAGGTTTGCCGGGAGGGGACAGGAA GCTCACCCAGCAGCTGGCGCAGGCCACCGGCAGGCCCCCCCAGGTTTGCCGGGAGGGGACAGGAA A G AP000350.4,MIF Ensembl:ENSG00000251357,Ensembl:ENSG00000240972 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr22:23894351..23895194;chr22:23894376..23895200;chr22:23894376..23894825;chr22:23894376..23894875;chr22:23894351..23894613;chr22:23894425..23894623 26863196,32194978 MeRIP-seq:(Medium) rs1011804555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246365,Human_RBP_ID_576612,Human_RBP_ID_781757,Human_RBP_ID_932131,Human_RBP_ID_4708099,Human_RBP_ID_17660430,Human_RBP_ID_18194061,Human_RBP_ID_22454382,Human_RBP_ID_26822316 Human_Splice_Rec_2144785,Human_Splice_Rec_2144789 RMVar_hsa_circ_78844,RMVar_hsa_circ_213300 89834 RMVar_ID_89834 Human_SNP_ID_699966383 m1A Human chr22 - 23895167 23895167 23895167 CCCACCAGAAGGTTGGGGTGGGCGGGCCTAGAACACAGCGTGCGGCGGGTTCCCGGGTGGAGCCA CCCACCAGAAGGTTGGGGTGGGCGGGCCTAGACCACAGCGTGCGGCGGGTTCCCGGGTGGAGCCA T G MIF-AS1 Ensembl:ENSG00000218537 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23895021..23895171 26863196 MeRIP-seq:(Medium) rs770361893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18497594,Human_RBP_ID_26500820 89835 RMVar_ID_89835 Human_SNP_ID_699970889 m1A Human chr22 - 23913282 23913282 23913282 GGGACAGTGGCAAGGGATGCCAGGAGAAGGTGAGGGAGAGGACACATGAGTGTTAGGTTTTTGAA GGGACAGTGGCAAGGGATGCCAGGAGAAGGTGGGGGAGAGGACACATGAGTGTTAGGTTTTTGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23913275..23913343 26863196 MeRIP-seq:(Medium) rs1037100819 Functional Loss SNV dbSNP153 33..33 33 - - - 89836 RMVar_ID_89836 Human_SNP_ID_699975445 m1A Human chr22 - 23930222 23930222 23930222 CATCTTCCCAGATGCTGGCGCTACTGCTGGACAAAGGAGCCCTCTGGTGGCCCTGTCCGGGCATA CATCTTCCCAGATGCTGGCGCTACTGCTGGACTAAGGAGCCCTCTGGTGGCCCTGTCCGGGCATA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:23930199..23930331 32194978 MeRIP-seq:(Medium) rs1349612009 Functional Loss SNV dbSNP153 33..33 33 - - - 89837 RMVar_ID_89837 Human_SNP_ID_699982664 m1A Human chr22 - 23958460 23958460 23958460 GGCCATAGACTGACCCACTCTCTGCCCCCATCAGGTGTTGGGGCCACTCATTGGGGTCCAGGTGC GGCCATAGACTGACCCACTCTCTGCCCCCATCGGGTGTTGGGGCCACTCATTGGGGTCCAGGTGC T C GSTT2B Ensembl:ENSG00000133433 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23958458..23958532 26863196 MeRIP-seq:(Medium) rs780993008 Functional Loss SNV dbSNP153 33..33 33 - - - 89838 RMVar_ID_89838 Human_SNP_ID_699983228 m1A Human chr22 - 23960199 23960199 23960199 GGCCCCGGGCCCCAGTGGCCCTCCCATACCCCATGGGGCAGCGAGGGAGGGGAAAGGCGAGGGAT GGCCCCGGGCCCCAGTGGCCCTCCCATACCCCGTGGGGCAGCGAGGGAGGGGAAAGGCGAGGGAT T C GSTT2B Ensembl:ENSG00000133433 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23960193..23960308 26863196 MeRIP-seq:(Medium) rs1220361901 Functional Loss SNV dbSNP153 33..33 33 - - - 89839 RMVar_ID_89839 Human_SNP_ID_699995078 m1A Human chr22 - 24011369 24011369 24011369 GCACCGCCTTCAAACCAGCCTTCCAGGAACTCACCAGGCGTCTCCACAGCAACGGCCAGTCTGTC GCACCGCCTTCAAACCAGCCTTCCAGGAACTCTCCAGGCGTCTCCACAGCAACGGCCAGTCTGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:24011347..24011532 26863196 MeRIP-seq:(Medium) rs1313543046 Functional Loss SNV dbSNP153 33..33 33 - - - 89840 RMVar_ID_89840 Human_SNP_ID_700018005 m1A Human chr22 + 24103210 24103210 24103210 TGTTTGATGCGCTTGGCTTCTGCTGATGGCCTATCCTCCCAGTTCTGGCCAGAGGCAGATGCGGT TGTTTGATGCGCTTGGCTTCTGCTGATGGCCTGTCCTCCCAGTTCTGGCCAGAGGCAGATGCGGT A G AC253536.3,CABIN1 Ensembl:ENSG00000232545,Ensembl:ENSG00000099991 lincRNA,Protein coding exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24103186..24103304 32194978 MeRIP-seq:(Medium) rs547593131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1101933,Human_RBP_ID_20731909,Human_RBP_ID_21985784,Human_RBP_ID_22480158,Human_RBP_ID_22819842,Human_RBP_ID_23938149 Human_miRNA_ID_3147439,Human_miRNA_ID_3179392 RMVar_hsa_circ_571,RMVar_hsa_circ_5056,RMVar_hsa_circ_38435,RMVar_hsa_circ_338701,RMVar_hsa_circ_282206,RMVar_hsa_circ_310107,RMVar_hsa_circ_320521 89841 RMVar_ID_89841 Human_SNP_ID_700034684 m1A Human chr22 + 24171833 24171833 24171833 ACCCTGTGCCAGCTGACTCTGTCCAGCGGCCCAGTGATGCTCACACCAAGCCTCGCCCTGCACTA ACCCTGTGCCAGCTGACTCTGTCCAGCGGCCCGGTGATGCTCACACCAAGCCTCGCCCTGCACTA A G CABIN1 Ensembl:ENSG00000099991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24171783..24171915 26863196 MeRIP-seq:(Medium) rs774748257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23011427 RMVar_hsa_circ_362313,RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 89842 RMVar_ID_89842 Human_SNP_ID_700036262 m1A Human chr22 + 24177634 24177634 24177634 AAGGCCCCCAGCAGTGGGAGTGCCCAGCCACCAGAGGGTCACCCAGGCAAGCCTGAGCCCAGCCG AAGGCCCCCAGCAGTGGGAGTGCCCAGCCACCGGAGGGTCACCCAGGCAAGCCTGAGCCCAGCCG A G CABIN1 Ensembl:ENSG00000099991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:24177584..24177756 26863196 MeRIP-seq:(Medium) rs1276186463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9333326 RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 89843 RMVar_ID_89843 Human_SNP_ID_700036309 m1A Human chr22 + 24177749 24177749 24177749 CCGCCACCAAGTTCCCCCCTGAGATCACCGTCACGCCACCCACCCCAACCCTGCTCTCCCCCAAA CCGCCACCAAGTTCCCCCCTGAGATCACCGTCTCGCCACCCACCCCAACCCTGCTCTCCCCCAAA A T CABIN1 Ensembl:ENSG00000099991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24177642..24177825 26863196 MeRIP-seq:(Medium) rs1235425759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2144983,Human_Splice_Rec_2145053,Human_Splice_Rec_2145123,Human_Splice_Rec_2145211,Human_Splice_Rec_2145235 RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 89844 RMVar_ID_89844 Human_SNP_ID_700057347 m1A Human chr22 - 24248058 24248058 24248058 GGAGCCTGCTGGCTACTGAGTGCTCCAGGCGGACAAGGCTGACAAGCAATCTAGGGACAAGATAC GGAGCCTGCTGGCTACTGAGTGCTCCAGGCGGGCAAGGCTGACAAGCAATCTAGGGACAAGATAC T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:24248039..24248121 26863410 MeRIP-seq:(Medium) rs1225985030 Functional Loss SNV dbSNP153 33..33 33 - - - 89845 RMVar_ID_89845 Human_SNP_ID_700064644 m1A Human chr22 + 24270965 24270965 24270965 ACCGCCCAGCCCAAACCAGGAGATTGCGAGGGAGCGATGCGGTGCAGCGCGGTAAGAGCAGCAGC ACCGCCCAGCCCAAACCAGGAGATTGCGAGGGGGCGATGCGGTGCAGCGCGGTAAGAGCAGCAGC A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding 5'UTR,5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:24270916..24276732 32194978 MeRIP-seq:(Medium) rs1349670865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708515,Human_RBP_ID_7066467,Human_RBP_ID_17983119,Human_RBP_ID_18423621,Human_RBP_ID_19008800,Human_RBP_ID_23938236 Human_Splice_Rec_2145409,Human_Splice_Rec_2145439,Human_Splice_Rec_2145451,Human_Splice_Rec_2145483,Human_Splice_Rec_2145519,Human_Splice_Rec_2145527,Human_Splice_Rec_2145561 89846 RMVar_ID_89846 Human_SNP_ID_700101776 m1A Human chr22 - 24415052 24415052 24415052 TGACTCTCCTTCTGGGTTCTCACCAGCACCGGAACCCACCCCAGCCAATAGTCAGGAAGTGCCGC TGACTCTCCTTCTGGGTTCTCACCAGCACCGGTACCCACCCCAGCCAATAGTCAGGAAGTGCCGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24414850..24415150 32194978 MeRIP-seq:(Medium) rs976914215 Functional Loss SNV dbSNP153 33..33 33 - - - 89847 RMVar_ID_89847 Human_SNP_ID_700101777 m1A Human chr22 - 24415052 24415052 24415052 TGACTCTCCTTCTGGGTTCTCACCAGCACCGGAACCCACCCCAGCCAATAGTCAGGAAGTGCCGC TGACTCTCCTTCTGGGTTCTCACCAGCACCGGCACCCACCCCAGCCAATAGTCAGGAAGTGCCGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24414850..24415150 32194978 MeRIP-seq:(Medium) rs976914215 Functional Loss SNV dbSNP153 33..33 33 - - - 89848 RMVar_ID_89848 Human_SNP_ID_700104462 m1A Human chr22 + 24423598 24423598 24423598 GGCCCGGAGCGCTCCAAGGGGCGGGGAAGGGGACTCCCAGGCCCGAGGACTCCTGGAAGGGAGGT GGCCCGGAGCGCTCCAAGGGGCGGGGAAGGGGGCTCCCAGGCCCGAGGACTCCTGGAAGGGAGGT A G ADORA2A,SPECC1L-ADORA2A Ensembl:ENSG00000128271,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:24423548..24423767 26863196 MeRIP-seq:(Medium) rs886934534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2145607,Human_Splice_Rec_2145609 89849 RMVar_ID_89849 Human_SNP_ID_700104563 m1A Human chr22 + 24423877 24423877 24423877 GCGGGGGCAGCGCGGGTCTCAAAGCTGCCTGCAGGGGGCGCCCGTGAGCGGCGCGGCCGGAGCCG GCGGGGGCAGCGCGGGTCTCAAAGCTGCCTGCTGGGGGCGCCCGTGAGCGGCGCGGCCGGAGCCG A T ADORA2A,SPECC1L-ADORA2A Ensembl:ENSG00000128271,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:24423856..24423921 26863196 MeRIP-seq:(Medium) rs1053983169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2145605,Human_Splice_Rec_2145613 89850 RMVar_ID_89850 Human_SNP_ID_700104601 m1A Human chr22 - 24423959 24423959 24423959 GACCCCGCACGCCAGACCTAGCACCCCGGCTGACCTGCCGCTCGCACGCCGGCTCCCGCTGTCTC GACCCCGCACGCCAGACCTAGCACCCCGGCTGCCCTGCCGCTCGCACGCCGGCTCCCGCTGTCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:24423938..24424021 26863196 MeRIP-seq:(Medium) rs1031588056 Functional Loss SNV dbSNP153 33..33 33 - - - 89851 RMVar_ID_89851 Human_SNP_ID_700107471 m1A Human chr22 - 24433716 24433716 24433716 GGCCCTGCTCACCGGAGCGGGATGCGGATGGCAATGTAGCGGTCAATGGCGATGGCCAGGAGACT GGCCCTGCTCACCGGAGCGGGATGCGGATGGCCATGTAGCGGTCAATGGCGATGGCCAGGAGACT T G ADORA2A-AS1 Ensembl:ENSG00000178803 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24433667..24440813 32194978 MeRIP-seq:(Medium) rs1485953994 Functional Loss SNV dbSNP153 33..33 33 - - - 89852 RMVar_ID_89852 Human_SNP_ID_700107472 m1A Human chr22 - 24433716 24433716 24433716 GGCCCTGCTCACCGGAGCGGGATGCGGATGGCAATGTAGCGGTCAATGGCGATGGCCAGGAGACT GGCCCTGCTCACCGGAGCGGGATGCGGATGGCTATGTAGCGGTCAATGGCGATGGCCAGGAGACT T A ADORA2A-AS1 Ensembl:ENSG00000178803 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24433667..24440813 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89853 RMVar_ID_89853 Human_SNP_ID_700137700 m1A Human chr22 + 24555030 24555030 24555030 GGCGGCGCGGGGCGCCCATGGCCCCGGCCCAGAGCGGGCTACAGCTTCCGCTTCGGCTGGGGCGG GGCGGCGCGGGGCGCCCATGGCCCCGGCCCAGGGCGGGCTACAGCTTCCGCTTCGGCTGGGGCGG A G NONHSAG045678.2-001 RNACentral:URS00008C2DD0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24554985..24555090 26863196 MeRIP-seq:(Medium) rs1431334626 Functional Loss SNV dbSNP153 33..33 33 - - - 89854 RMVar_ID_89854 Human_SNP_ID_700137722 m1A Human chr22 + 24555084 24555084 24555084 GGCTGGGGCGGGAGGGCGGTCGGTGCGTGTCGAGTTCCTTCTCCGCCACCGCCGCCGCTGCGGAG GGCTGGGGCGGGAGGGCGGTCGGTGCGTGTCGGGTTCCTTCTCCGCCACCGCCGCCGCTGCGGAG A G NONHSAG045678.2-001 RNACentral:URS00008C2DD0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:24554919..24555133 26863196 MeRIP-seq:(Medium) rs1002324054 Functional Loss SNV dbSNP153 33..33 33 - - - 89855 RMVar_ID_89855 Human_SNP_ID_700138668 m1A Human chr22 + 24557779 24557779 24557779 GGTGAGGTATATCGGGGGAAGCTCATTGAAGCAGAGGACAACATGAACTGCCAGGTATTCTGCTT GGTGAGGTATATCGGGGGAAGCTCATTGAAGCGGAGGACAACATGAACTGCCAGGTATTCTGCTT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:24557625..24557842 26863196 MeRIP-seq:(Medium) rs1455592644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576794,Human_RBP_ID_1028632,Human_RBP_ID_1609043,Human_RBP_ID_1940569,Human_RBP_ID_2713663,Human_RBP_ID_4708520,Human_RBP_ID_7066909,Human_RBP_ID_9392074,Human_RBP_ID_14419841,Human_RBP_ID_18535130,Human_RBP_ID_18785883,Human_RBP_ID_22454865,Human_RBP_ID_22507718,Human_RBP_ID_23938393,Human_RBP_ID_26344886,Human_RBP_ID_26822990 Human_Splice_Rec_2145831,Human_Splice_Rec_2145837,Human_Splice_Rec_2145845,Human_Splice_Rec_2145883,Human_Splice_Rec_2145895 Human_miRNA_ID_2255805,Human_miRNA_ID_2571531,Human_miRNA_ID_3045267 RMVar_hsa_circ_89426,RMVar_hsa_circ_105930,RMVar_hsa_circ_213351,RMVar_hsa_circ_213352,RMVar_hsa_circ_213353,RMVar_hsa_circ_89548,RMVar_hsa_circ_348102 89856 RMVar_ID_89856 Human_SNP_ID_700142419 m1A Human chr22 - 24572068 24572066 24572068 CATTTCCCCTGATCTAAAGAGAAAGATGGCAAAAGATACCTAGCATATATGCACAAGCACCCACT CATTTCCCCTGATCTAAAGAGAAAGATGGCAA__GATACCTAGCATATATGCACAAGCACCCACT CTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:24571901..24572125 32194978 MeRIP-seq:(Medium) rs1037183323 Functional Loss DEL dbSNP153 33..34 33 - - - 89857 RMVar_ID_89857 Human_SNP_ID_700142555 m1A Human chr22 + 24572605 24572605 24572605 CAATATGGTGAAACCTCGTGTGTACTAAAAATAAAAAAATTAGCCGGGTGCGGTGGCATGTACCT CAATATGGTGAAACCTCGTGTGTACTAAAAATTAAAAAATTAGCCGGGTGCGGTGGCATGTACCT A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12172173 Functional Loss SNV dbSNP153 33..33 33 - - - 89858 RMVar_ID_89858 Human_SNP_ID_700143001 m1A Human chr22 + 24574596 24574596 24574596 AGACGGTCTCACTCTTCCCCAGGCGGGAGTGCAATGGCACAATCATGGCTCACTGCAGCCTCAAC AGACGGTCTCACTCTTCCCCAGGCGGGAGTGCTATGGCACAATCATGGCTCACTGCAGCCTCAAC A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1255593609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497191 89859 RMVar_ID_89859 Human_SNP_ID_700147018 m1A Human chr22 + 24589900 24589900 24589900 GGGAGATGGGGTCGACCGGGTTGAGGAAGGCCACATCTCTGTAGAGGATATCAGGAAGGAGGGTC GGGAGATGGGGTCGACCGGGTTGAGGAAGGCCCCATCTCTGTAGAGGATATCAGGAAGGAGGGTC A C GGT1 Ensembl:ENSG00000286070 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24589850..24592218 32194978 MeRIP-seq:(Medium) rs1313426326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14420674 89860 RMVar_ID_89860 Human_SNP_ID_700147019 m1A Human chr22 + 24589900 24589900 24589900 GGGAGATGGGGTCGACCGGGTTGAGGAAGGCCACATCTCTGTAGAGGATATCAGGAAGGAGGGTC GGGAGATGGGGTCGACCGGGTTGAGGAAGGCCGCATCTCTGTAGAGGATATCAGGAAGGAGGGTC A G GGT1 Ensembl:ENSG00000286070 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:24589850..24592218 32194978 MeRIP-seq:(Medium) rs1313426326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14420674 89861 RMVar_ID_89861 Human_SNP_ID_700147842 m1A Human chr22 - 24593053 24593053 24593053 AGACAGCCCGGCCTCCTGTGGGTTCGGCGACCATCGCGCGGCGGCCATGGGGGCGCGGCTGGGCC AGACAGCCCGGCCTCCTGTGGGTTCGGCGACCGTCGCGCGGCGGCCATGGGGGCGCGGCTGGGCC T C LRRC75B Ensembl:ENSG00000178026 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24592564..24593065 26863196 MeRIP-seq:(Medium) rs552282051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708898,Human_RBP_ID_18423622 89862 RMVar_ID_89862 Human_SNP_ID_700150418 m1A Human chr22 + 24603251 24603251 24603251 ACCGGGCGTCGGGTGAGCCCAGAAGTGAGAGCAGTTGGCTGTGCCCCAGTGCTGTGTGACCCAGA ACCGGGCGTCGGGTGAGCCCAGAAGTGAGAGCTGTTGGCTGTGCCCCAGTGCTGTGTGACCCAGA A T GGT1,GGT1:2 Ensembl:ENSG00000286070,Ensembl:ENSG00000100031 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:24603212..24603296 26863196 MeRIP-seq:(Medium) rs1372098792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708112,Human_RBP_ID_14420774,Human_RBP_ID_22454592 Human_Splice_Rec_2146045,Human_Splice_Rec_2146083,Human_Splice_Rec_2146097,Human_Splice_Rec_2146105,Human_Splice_Rec_2146127,Human_Splice_Rec_2146159 89863 RMVar_ID_89863 Human_SNP_ID_700150420 m1A Human chr22 - 24603260 24603260 24603260 AGCGGCGCCTCTGGGTCACACAGCACTGGGGCACAGCCAACTGCTCTCACTTCTGGGCTCACCCG AGCGGCGCCTCTGGGTCACACAGCACTGGGGCGCAGCCAACTGCTCTCACTTCTGGGCTCACCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24603213..24603290 26863196 MeRIP-seq:(Medium) rs199770536 Functional Loss SNV dbSNP153 33..33 33 - - - 89864 RMVar_ID_89864 Human_SNP_ID_700156824 m1A Human chr22 + 24623053 24623053 24623053 CCCCCAACACCACTGCTGCAGCTCCATCCTCCACGCAGTGGTGCAGCCCCATCCCAGCACCCATT CCCCCAACACCACTGCTGCAGCTCCATCCTCCCCGCAGTGGTGCAGCCCCATCCCAGCACCCATT A C GGT1,GGT1:2 Ensembl:ENSG00000286070,Ensembl:ENSG00000100031 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:24623052..24623127 26863196 MeRIP-seq:(Medium) rs1407047335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80300,RMVar_hsa_circ_73735,RMVar_hsa_circ_213361 89865 RMVar_ID_89865 Human_SNP_ID_700160304 m1A Human chr22 - 24633752 24633748 24633753 CACTCATAGTCACACACACCCTCACACAGCAAAACACAATCACACACGTTCACACCCACCCACAC CACTCATAGTCACACACACCCTCACACAGCA_____CAATCACACACGTTCACACCCACCCACAC GTGTTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:24633707..24633933 26863196 MeRIP-seq:(Medium) rs1408192111 Functional Loss DEL dbSNP153 32..36 33 - - - 89866 RMVar_ID_89866 Human_SNP_ID_700160305 m1A Human chr22 - 24633752 24633750 24633752 CACTCATAGTCACACACACCCTCACACAGCAAAACACAATCACACACGTTCACACCCACCCACAC CACTCATAGTCACACACACCCTCACACAGCAA__CACAATCACACACGTTCACACCCACCCACAC GTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:24633707..24633933 26863196 MeRIP-seq:(Medium) rs1049703464 Functional Loss DEL dbSNP153 33..34 33 - - - 89867 RMVar_ID_89867 Human_SNP_ID_700265772 m1A Human chr22 + 25028364 25028364 25028364 CGGCTTGGTGGGGCAGGAGGTGGGCAGTGGGGAGGGCCCGAGGACGAGCTCGCCCCTCTTCAACA CGGCTTGGTGGGGCAGGAGGTGGGCAGTGGGGGGGGCCCGAGGACGAGCTCGCCCCTCTTCAACA A G KIAA1671 Ensembl:ENSG00000197077 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:25028012..25028612 32194978 MeRIP-seq:(Medium) rs759033748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529846 RMVar_hsa_circ_40023,RMVar_hsa_circ_308931,RMVar_hsa_circ_305873,RMVar_hsa_circ_327885,RMVar_hsa_circ_369099 89868 RMVar_ID_89868 Human_SNP_ID_700272904 m1A Human chr22 + 25058711 25058711 25058711 TAATGAACCATCACAGAACTTAGGGGTGTAACAGGGTCATGGATTCCGCAGGTCAAGAAGCCAAG TAATGAACCATCACAGAACTTAGGGGTGTAACGGGGTCATGGATTCCGCAGGTCAAGAAGCCAAG A G KIAA1671 Ensembl:ENSG00000197077 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:25058709..25058820 26863196 MeRIP-seq:(Medium) rs182317008 Functional Loss SNV dbSNP153 33..33 33 - - - 89869 RMVar_ID_89869 Human_SNP_ID_700350923 m1A Human chr22 + 25350791 25350791 25350791 CCGCTGCCCCGCACAGCTGCGCCACTGGCTTCAGCACCACCGTGACTCCCTTCAGCCCCTTCGCT CCGCTGCCCCGCACAGCTGCGCCACTGGCTTCGGCACCACCGTGACTCCCTTCAGCCCCTTCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:25350745..25350926 26863196 MeRIP-seq:(Medium) rs974724763 Functional Loss SNV dbSNP153 33..33 33 - - - 89870 RMVar_ID_89870 Human_SNP_ID_700356661 m1A Human chr22 - 25367727 25367727 25367727 GTGCTGGTGGGACTTGTGCCTGTTCCGGAGGGAGGCATTGGGAGTGACGTTTAGGCTGAGAGGAT GTGCTGGTGGGACTTGTGCCTGTTCCGGAGGGGGGCATTGGGAGTGACGTTTAGGCTGAGAGGAT T C LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:25367608..25367889 26863196 MeRIP-seq:(Medium) rs1158696937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833318,Human_RBP_ID_17148390 RMVar_hsa_circ_86546,RMVar_hsa_circ_120615,RMVar_hsa_circ_34765,RMVar_hsa_circ_114668,RMVar_hsa_circ_117364,RMVar_hsa_circ_213387,RMVar_hsa_circ_213388,RMVar_hsa_circ_213390,RMVar_hsa_circ_348886,RMVar_hsa_circ_213394,RMVar_hsa_circ_105891,RMVar_hsa_circ_94193,RMVar_hsa_circ_213395,RMVar_hsa_circ_213396 89871 RMVar_ID_89871 Human_SNP_ID_700356722 m1A Human chr22 + 25367907 25367906 25367907 TCCGCGTGTGACCCCAGGGCCTCCTCTGCCTGACTCTGAATTCCACTGCCCAACGTGACACCTCG TCCGCGTGTGACCCCAGGGCCTCCTCTGCCTG_CTCTGAATTCCACTGCCCAACGTGACACCTCG GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:25367891..25368005 32194978 MeRIP-seq:(Medium) rs1385773836 Functional Loss DEL dbSNP153 33..33 33 - - - 89872 RMVar_ID_89872 Human_SNP_ID_700367086 m1A Human chr22 - 25405359 25405359 25405359 GCGCCCAACGGGGAAGACGAAGATGCAGGGACACGCGCGAGGAGCCGCCGCAGCCGCCGCCGCCG GCGCCCAACGGGGAAGACGAAGATGCAGGGACCCGCGCGAGGAGCCGCCGCAGCCGCCGCCGCCG T G LRP5L Ensembl:ENSG00000100068 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:25405255..25405394 26863196 MeRIP-seq:(Medium) rs1220682839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392719,Human_RBP_ID_18423712,Human_RBP_ID_23015486 89873 RMVar_ID_89873 Human_SNP_ID_700367090 m1A Human chr22 - 25405365 25405365 25405365 TCCGCGGCGCCCAACGGGGAAGACGAAGATGCAGGGACACGCGCGAGGAGCCGCCGCAGCCGCCG TCCGCGGCGCCCAACGGGGAAGACGAAGATGCGGGGACACGCGCGAGGAGCCGCCGCAGCCGCCG T C LRP5L Ensembl:ENSG00000100068 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:25405230..25405381 26863196 MeRIP-seq:(Medium) rs1013769329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392719,Human_RBP_ID_18423712 89874 RMVar_ID_89874 Human_SNP_ID_700378673 m1A Human chr22 - 25448170 25448170 25448170 TCTCCCCAGGACGGGGCTCCAAGTGGTCCCCAAGCCGCCGCGGTGCCCCCTGAGGCGGGTCCTGA TCTCCCCAGGACGGGGCTCCAAGTGGTCCCCAGGCCGCCGCGGTGCCCCCTGAGGCGGGTCCTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:25448119..25448244 26863196 MeRIP-seq:(Medium) rs981258457 Functional Loss SNV dbSNP153 33..33 33 - - - 89875 RMVar_ID_89875 Human_SNP_ID_700378678 m1A Human chr22 + 25448185 25448185 25448185 GGGGGCACCGCGGCGGCTTGGGGACCACTTGGAGCCCCGTCCTGGGGAGAAAACAGCTCACGTCT GGGGGCACCGCGGCGGCTTGGGGACCACTTGGGGCCCCGTCCTGGGGAGAAAACAGCTCACGTCT A G CRYBB2P1 Ensembl:ENSG00000100058 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:25448135..25448229 26863196 MeRIP-seq:(Medium) rs1227856715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576924,Human_RBP_ID_930707,Human_RBP_ID_5205505,Human_RBP_ID_5600146,Human_RBP_ID_14423059,Human_RBP_ID_18423713,Human_RBP_ID_19008819,Human_RBP_ID_27821554 Human_Splice_Rec_2147063 89876 RMVar_ID_89876 Human_SNP_ID_700378700 m1A Human chr22 - 25448244 25448235 25448244 AAAAAATGCCCCGGAGAAGCTGAGCTGCACGCAGCTCCCGCCTAAGCAGTCAGGGCCATAGACGT AAAAAATGCCCCGGAGAAGCTGAGCTGCACGC_________CTAAGCAGTCAGGGCCATAGACGT GGCGGGAGCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:25448193..25448329 32194978 MeRIP-seq:(Medium) rs1260222275 Functional Loss DEL dbSNP153 33..41 33 - - - 89877 RMVar_ID_89877 Human_SNP_ID_700378708 m1A Human chr22 - 25448259 25448259 25448259 TACTCACCGTGTAGAAAAAAATGCCCCGGAGAAGCTGAGCTGCACGCAGCTCCCGCCTAAGCAGT TACTCACCGTGTAGAAAAAAATGCCCCGGAGAGGCTGAGCTGCACGCAGCTCCCGCCTAAGCAGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:25448201..25448300 26863196 MeRIP-seq:(Medium) rs1333555242 Functional Loss SNV dbSNP153 33..33 33 - - - 89878 RMVar_ID_89878 Human_SNP_ID_700381840 m1A Human chr22 + 25459553 25459553 25459553 GTCCGTGCGCTGCATCCACGACATGCAGGGGCACCAATGTGGTGCCTTCCACCCCTCCAACTAGT GTCCGTGCGCTGCATCCACGACATGCAGGGGCGCCAATGTGGTGCCTTCCACCCCTCCAACTAGT A G CRYBB2P1 Ensembl:ENSG00000100058 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:25459504..25459587 26863196 MeRIP-seq:(Medium) rs1273896364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962261,Human_RBP_ID_9392722,Human_RBP_ID_19008822,Human_RBP_ID_19112918 89879 RMVar_ID_89879 Human_SNP_ID_700389351 m1A Human chr22 + 25487352 25487352 25487352 GAGTGGATGGGTGGGTGGATGGATGAGTGGAAAGGTGGGTGTAAGGGTAGGTGGATGGGTGGATA GAGTGGATGGGTGGGTGGATGGATGAGTGGAAGGGTGGGTGTAAGGGTAGGTGGATGGGTGGATA A G CRYBB2P1 Ensembl:ENSG00000100058 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:25487141..25487761 26863196 MeRIP-seq:(Medium) rs1490011279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5653430,Human_RBP_ID_8207273,Human_RBP_ID_9433775,Human_RBP_ID_23939049 89880 RMVar_ID_89880 Human_SNP_ID_700389354 m1A Human chr22 - 25487361 25487361 25487361 CCATTCATCTATCCACCCATCCACCTACCCTTACACCCACCTTTCCACTCATCCATCCACCCACC CCATTCATCTATCCACCCATCCACCTACCCTTCCACCCACCTTTCCACTCATCCATCCACCCACC T G lnc-LRP5L-8 RNACentral:URS00009BA84E lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:25487315..25487444 26863196 MeRIP-seq:(Medium) rs1456785007 Functional Loss SNV dbSNP153 33..33 33 - - - 89881 RMVar_ID_89881 Human_SNP_ID_700395346 m1A Human chr22 + 25510688 25510688 25510688 CCATGCCTGGCTCTAGGCTTTGGGACAGTTCAACTCTGTTCCACATGTCTGATTCTGGATCCCAT CCATGCCTGGCTCTAGGCTTTGGGACAGTTCAGCTCTGTTCCACATGTCTGATTCTGGATCCCAT A G lnc-LRP5L-8 RNACentral:URS00009BA84E lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1049640409 Functional Loss SNV dbSNP153 33..33 33 - - - 89882 RMVar_ID_89882 Human_SNP_ID_700637815 m1A Human chr22 + 26483717 26483717 26483717 GGCATCCCAGTGCTCGGGGTTCGGGACTCTGGACCAGAAATGTGGGCAGCAGCTGGGTACCTGCG GGCATCCCAGTGCTCGGGGTTCGGGACTCTGGCCCAGAAATGTGGGCAGCAGCTGGGTACCTGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:26483714..26483785;chr22:26483714..26483801 26863196 MeRIP-seq:(Medium) rs1569144136 Functional Loss SNV dbSNP153 33..33 33 - - - 89883 RMVar_ID_89883 Human_SNP_ID_700637983 m1A Human chr22 + 26483982 26483982 26483982 GCGCTCCGCGGCTCGACGGCCGCGGCGGAGGGAGGCGGCGCCCCGGGGGAGAGAGGCGGCGCCCC GCGCTCCGCGGCTCGACGGCCGCGGCGGAGGGCGGCGGCGCCCCGGGGGAGAGAGGCGGCGCCCC A C SRRD Ensembl:ENSG00000100104 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:26483901..26488016 26863410 MeRIP-seq:(Medium) rs1384604996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708910 89884 RMVar_ID_89884 Human_SNP_ID_700642562 m1A Human chr22 - 26499537 26499537 26499537 GCACAACGTTCCCGATGATGGGCTGCCGCTACAGTCCCAACAGCTGCCACAGTCTGGCAAAGAGG GCACAACGTTCCCGATGATGGGCTGCCGCTACGGTCCCAACAGCTGCCACAGTCTGGCAAAGAGG T C TFIP11 Ensembl:ENSG00000100109 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:26499491..26501960 32194978 MeRIP-seq:(Medium) rs765279883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931728,Human_RBP_ID_8865669 Human_Splice_Rec_2148332,Human_Splice_Rec_2148360,Human_Splice_Rec_2148388,Human_Splice_Rec_2148414,Human_Splice_Rec_2148444,Human_Splice_Rec_2148464,Human_Splice_Rec_2148470 RMVar_hsa_circ_36814,RMVar_hsa_circ_27624,RMVar_hsa_circ_43273,RMVar_hsa_circ_213481,RMVar_hsa_circ_325921,RMVar_hsa_circ_213483,RMVar_hsa_circ_372274 89885 RMVar_ID_89885 Human_SNP_ID_700642570 m1A Human chr22 + 26499554 26499554 26499554 GGCAGCTGTTGGGACTGTAGCGGCAGCCCATCATCGGGAACGTTGTGCTTGTGGCTGATCTGACT GGCAGCTGTTGGGACTGTAGCGGCAGCCCATCGTCGGGAACGTTGTGCTTGTGGCTGATCTGACT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:26499456..26499558 26863410 MeRIP-seq:(Medium) rs147982713 Functional Loss SNV dbSNP153 33..33 33 - - - 89886 RMVar_ID_89886 Human_SNP_ID_700643675 m1A Human chr22 - 26503719 26503719 26503719 GTGCTGTGGGGGCTTATGGATCCGAGCGCACCACTCAGTCCATGCAAGACTTCCCTGTGGTTGAC GTGCTGTGGGGGCTTATGGATCCGAGCGCACCGCTCAGTCCATGCAAGACTTCCCTGTGGTTGAC T C TFIP11 Ensembl:ENSG00000100109 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:26502058..26503780 32194978 MeRIP-seq:(Medium) rs1268751194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18786153 Human_Splice_Rec_2148328,Human_Splice_Rec_2148329,Human_Splice_Rec_2148356,Human_Splice_Rec_2148357,Human_Splice_Rec_2148384,Human_Splice_Rec_2148385,Human_Splice_Rec_2148410,Human_Splice_Rec_2148411,Human_Splice_Rec_2148440,Human_Splice_Rec_2148441,Human_Splice_Rec_2148460,Human_Splice_Rec_2148461,Human_Splice_Rec_2148466,Human_Splice_Rec_2148467,Human_Splice_Rec_2148472,Human_Splice_Rec_2148473 RMVar_hsa_circ_36814,RMVar_hsa_circ_43273,RMVar_hsa_circ_354189,RMVar_hsa_circ_213483,RMVar_hsa_circ_372274 89887 RMVar_ID_89887 Human_SNP_ID_700643694 m1A Human chr22 - 26503766 26503766 26503766 CTCAGGTATCATTAACCCAATTGAAGCCAAGCAGAGAAAGGGAAAAGGTGCTGTGGGGGCTTATG CTCAGGTATCATTAACCCAATTGAAGCCAAGCGGAGAAAGGGAAAAGGTGCTGTGGGGGCTTATG T C TFIP11 Ensembl:ENSG00000100109 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:26503723..26503887 26863196 MeRIP-seq:(Medium) rs749485260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64997,Human_RBP_ID_4690024 Human_Splice_Rec_2148328,Human_Splice_Rec_2148356,Human_Splice_Rec_2148384,Human_Splice_Rec_2148410,Human_Splice_Rec_2148440,Human_Splice_Rec_2148460,Human_Splice_Rec_2148466,Human_Splice_Rec_2148472 RMVar_hsa_circ_36814,RMVar_hsa_circ_43273,RMVar_hsa_circ_354189,RMVar_hsa_circ_213483,RMVar_hsa_circ_372274 89888 RMVar_ID_89888 Human_SNP_ID_700653127 m1A Human chr22 - 26541556 26541556 26541556 GCCCTGGTCCTGGTGCTGGCGGTTCAGCTGGGACAGCAGGTGCTAGAGTGCCGGGCGGTGCTGGC GCCCTGGTCCTGGTGCTGGCGGTTCAGCTGGGGCAGCAGGTGCTAGAGTGCCGGGCGGTGCTGGC T C TPST2 Ensembl:ENSG00000128294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:26541506..26541577 26863196 MeRIP-seq:(Medium) rs774412530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708912,Human_RBP_ID_9300318,Human_RBP_ID_17148110 Human_miRNA_ID_1968936,Human_miRNA_ID_2513480,Human_miRNA_ID_3056301 RMVar_hsa_circ_358958,RMVar_hsa_circ_213492,RMVar_hsa_circ_213490,RMVar_hsa_circ_292536,RMVar_hsa_circ_317479,RMVar_hsa_circ_273611,RMVar_hsa_circ_293507,RMVar_hsa_circ_213491 89889 RMVar_ID_89889 Human_SNP_ID_700660977 m1A Human chr22 - 26571188 26571188 26571188 GAGTGACAGCAAGGGGGCCAGCGTGGCTGGAGAAGAGGCAAGGGCCAGTGGGGTTGGGGGCAGAA GAGTGACAGCAAGGGGGCCAGCGTGGCTGGAGGAGAGGCAAGGGCCAGTGGGGTTGGGGGCAGAA T C TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:26571183..26571371;chr22:26571183..26571351 26863196 MeRIP-seq:(Medium) rs138435352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22603345 89890 RMVar_ID_89890 Human_SNP_ID_700666013 m1A Human chr22 - 26590011 26590011 26590011 CCTGGGGCGGCAGGGGGTGGCCTCGGGTTGCAACCGGGGGCGCGGGCTGGGGGCCGTGCGGGTCG CCTGGGGCGGCAGGGGGTGGCCTCGGGTTGCATCCGGGGGCGCGGGCTGGGGGCCGTGCGGGTCG T A TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:26589999..26590092 26863196 MeRIP-seq:(Medium) rs11090449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676071,Human_RBP_ID_5387330,Human_RBP_ID_8118138,Human_RBP_ID_9332784,Human_RBP_ID_9433161,Human_RBP_ID_18423904,Human_RBP_ID_18498834,Human_RBP_ID_19111770 89891 RMVar_ID_89891 Human_SNP_ID_700666014 m1A Human chr22 - 26590011 26590011 26590011 CCTGGGGCGGCAGGGGGTGGCCTCGGGTTGCAACCGGGGGCGCGGGCTGGGGGCCGTGCGGGTCG CCTGGGGCGGCAGGGGGTGGCCTCGGGTTGCAGCCGGGGGCGCGGGCTGGGGGCCGTGCGGGTCG T C TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:26589999..26590092 26863196 MeRIP-seq:(Medium) rs11090449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676071,Human_RBP_ID_5387330,Human_RBP_ID_8118138,Human_RBP_ID_9332784,Human_RBP_ID_9433161,Human_RBP_ID_18423904,Human_RBP_ID_18498834,Human_RBP_ID_19111770 89892 RMVar_ID_89892 Human_SNP_ID_700688915 m1A Human chr22 + 26677895 26677895 26677895 AACCTTGAAGGATGGGGAATAGTCAATAAATCAGGAGAAAATAGTGATGGTGCAGGGCATTTCAG AACCTTGAAGGATGGGGAATAGTCAATAAATCCGGAGAAAATAGTGATGGTGCAGGGCATTTCAG A C MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:26677860..26678107 26863196 MeRIP-seq:(Medium) rs739312 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11659,GWAS_ID_11660,GWAS_ID_11661 89893 RMVar_ID_89893 Human_SNP_ID_700701461 m1A Human chr22 + 26726839 26726839 26726839 TGAGGATGGAGAATGTGAAAGAAAGTTTTCCTAGGGGGCTGGTCTTTGAGTGGAATCTTGAAAGT TGAGGATGGAGAATGTGAAAGAAAGTTTTCCTGGGGGGCTGGTCTTTGAGTGGAATCTTGAAAGT A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:26726788..26726987 26863196 MeRIP-seq:(Medium) rs1056987224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7068295 89894 RMVar_ID_89894 Human_SNP_ID_700951120 m1A Human chr22 - 27674767 27674765 27674768 GAGAAAGGGGGAAGAGAGAGAAAGGGAAAGAGAAAGAGAGAAAGGGAGAAAGGGAAAGGAGAGAG GAGAAAGGGGGAAGAGAGAGAAAGGGAAAGA___AGAGAGAAAGGGAGAAAGGGAAAGGAGAGAG TTTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:27674623..27674786 26863196 MeRIP-seq:(Medium) rs1359495811 Functional Loss DEL dbSNP153 32..34 33 - - - 89895 RMVar_ID_89895 Human_SNP_ID_700971928 m1A Human chr22 + 27757983 27757975 27757983 CCAAAGTCTGCCCACTTTTCTCCTGCCCCACTACCCCACCCTGGCCCACATACCAACCATCTCCT CCAAAGTCTGCCCACTTTTCTCCTG________CCCCACCCTGGCCCACATACCAACCATCTCCT GCCCCACTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:27757981..27758084 26863196 MeRIP-seq:(Medium) rs1310416653 Functional Loss DEL dbSNP153 26..33 33 - - - 89896 RMVar_ID_89896 Human_SNP_ID_700982779 m1A Human chr22 + 27798979 27798964 27798979 GCTGCTGCTGCTGCTGCTGCTGCTGCTGTTGCAGGGACTGGTGGTCCGGGGCCGGATGCTGCAGG GCTGCTGCTGCTGCTGCT_______________GGGACTGGTGGTCCGGGGCCGGATGCTGCAGG TGCTGCTGCTGTTGCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:27798928..27799017 26863196 MeRIP-seq:(Medium) rs1251698329 Functional Loss DEL dbSNP153 19..33 33 - - - 89897 RMVar_ID_89897 Human_SNP_ID_700982792 m1A Human chr22 + 27798979 27798979 27798979 GCTGCTGCTGCTGCTGCTGCTGCTGCTGTTGCAGGGACTGGTGGTCCGGGGCCGGATGCTGCAGG GCTGCTGCTGCTGCTGCTGCTGCTGCTGTTGCTGGGACTGGTGGTCCGGGGCCGGATGCTGCAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:27798928..27799017 26863196 MeRIP-seq:(Medium) rs769307303 Functional Loss SNV dbSNP153 33..33 33 - - - 89898 RMVar_ID_89898 Human_SNP_ID_700982990 m1A Human chr22 - 27799382 27799382 27799382 CGCTCCCTCGGCCCCAGCAGGGCGAGGCGGGCACGCCCAGCGGCGGCCTGCAGGACGGAGGCCCC CGCTCCCTCGGCCCCAGCAGGGCGAGGCGGGCGCGCCCAGCGGCGGCCTGCAGGACGGAGGCCCC T C MN1 Ensembl:ENSG00000169184 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:27799334..27799462 26863196 MeRIP-seq:(Medium) rs754233954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27492568 89899 RMVar_ID_89899 Human_SNP_ID_700983031 m1A Human chr22 - 27799471 27799471 27799471 CCCTCAGCAGCAGCCCCCGCAGCAGCCGCCACAGCAGCAGCCGCCGCCGCCACCCGGGCTTCTAG CCCTCAGCAGCAGCCCCCGCAGCAGCCGCCACCGCAGCAGCCGCCGCCGCCACCCGGGCTTCTAG T G MN1 Ensembl:ENSG00000169184 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:27799313..27799514 26863196 MeRIP-seq:(Medium) rs868192034 Functional Loss SNV dbSNP153 33..33 33 - - - 89900 RMVar_ID_89900 Human_SNP_ID_700983862 m1A Human chr22 - 27801508 27801508 27801508 CCCCCCTCCCTCAGGTCCGAGAGGGACTCGCGAAGCACCTCAGCGCGGAGGCAGGGAACCGGAGC CCCCCCTCCCTCAGGTCCGAGAGGGACTCGCGCAGCACCTCAGCGCGGAGGCAGGGAACCGGAGC T G MN1 Ensembl:ENSG00000169184 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:27801376..27801737 26863196 MeRIP-seq:(Medium) rs1237836048 Functional Loss SNV dbSNP153 33..33 33 - - - 89901 RMVar_ID_89901 Human_SNP_ID_700983946 m1A Human chr22 - 27801709 27801709 27801709 GGCGCTGGGCGAGAGGCAGACACAGAGAGGGGAGCCGAGACCCTCGGAACGCCCCACGCAGAGCC GGCGCTGGGCGAGAGGCAGACACAGAGAGGGGGGCCGAGACCCTCGGAACGCCCCACGCAGAGCC T C MN1 Ensembl:ENSG00000169184 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:27801659..27801725 26863196 MeRIP-seq:(Medium) rs1048316483 Functional Loss SNV dbSNP153 33..33 33 - - - 89902 RMVar_ID_89902 Human_SNP_ID_701008733 m1A Human chr22 + 27907488 27907484 27907488 GGACAGCAAATGGGCCCTGTTTTGCCCAGTTTATTTATTATTGGTTAGGTTTTTGTTCCTCACTA GGACAGCAAATGGGCCCTGTTTTGCCCAG____TTTATTATTGGTTAGGTTTTTGTTCCTCACTA GTTTA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:27907485..27907652 26863196 MeRIP-seq:(Medium) rs1338046623 Functional Loss DEL dbSNP153 30..33 33 - - - 89903 RMVar_ID_89903 Human_SNP_ID_701010398 m1A Human chr22 + 27914304 27914304 27914304 CAGTACATATACCAATAAAATGATGCAGAAGCAAGAAAAACTCACCTCCTGAACAGAACATGGCA CAGTACATATACCAATAAAATGATGCAGAAGCCAGAAAAACTCACCTCCTGAACAGAACATGGCA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:27914301..27914375 26863410 MeRIP-seq:(Medium) rs1428176467 Functional Loss SNV dbSNP153 33..33 33 - - - 89904 RMVar_ID_89904 Human_SNP_ID_701010404 m1A Human chr22 - 27914332 27914332 27914332 TTCTTTTGTCTTTTTAGCCGTGTGGTTTTGCCATGTTCTGTTCAGGAGGTGAGTTTTTCTTGCTT TTCTTTTGTCTTTTTAGCCGTGTGGTTTTGCCGTGTTCTGTTCAGGAGGTGAGTTTTTCTTGCTT T C PITPNB Ensembl:ENSG00000180957 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:27914326..27914375 26863410 MeRIP-seq:(Medium) rs1308007517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_932533,Human_RBP_ID_4690266,Human_RBP_ID_19008837,Human_RBP_ID_23940285,Human_RBP_ID_25660074 Human_Splice_Rec_2148988,Human_Splice_Rec_2148989,Human_Splice_Rec_2149010,Human_Splice_Rec_2149011,Human_Splice_Rec_2149030,Human_Splice_Rec_2149031,Human_Splice_Rec_2149048,Human_Splice_Rec_2149049,Human_Splice_Rec_2149086,Human_Splice_Rec_2149087,Human_Splice_Rec_2149102,Human_Splice_Rec_2149103,Human_Splice_Rec_2149118,Human_Splice_Rec_2149119,Human_Splice_Rec_2149126,Human_Splice_Rec_2149127 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514,RMVar_hsa_circ_280967,RMVar_hsa_circ_213517 89905 RMVar_ID_89905 Human_SNP_ID_701011596 m1A Human chr22 + 27919039 27919039 27919039 CACTCGCTGAGGGGCTTCGAAGGGGCCGGGGGAGGGAGGGGGCGCCCGCAGGGAGGGGCTGACAC CACTCGCTGAGGGGCTTCGAAGGGGCCGGGGGGGGGAGGGGGCGCCCGCAGGGAGGGGCTGACAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:27919028..27919169 26863196 MeRIP-seq:(Medium) rs1372374278 Functional Loss SNV dbSNP153 33..33 33 - - - 89906 RMVar_ID_89906 Human_SNP_ID_701011640 m1A Human chr22 - 27919112 27919112 27919112 GCCGTGGGACGGCAGTGATGGGAGATTTGTTGATGGAGAAGTGGTAGGATATTCCTAAATCGGAG GCCGTGGGACGGCAGTGATGGGAGATTTGTTGTTGGAGAAGTGGTAGGATATTCCTAAATCGGAG T A PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:27919109..27919208 26863410 MeRIP-seq:(Medium) rs1318659336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7069490,Human_RBP_ID_14432711,Human_RBP_ID_23940300 Human_Splice_Rec_2149047,Human_Splice_Rec_2149101 RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 89907 RMVar_ID_89907 Human_SNP_ID_701012576 m1A Human chr22 + 27922080 27922080 27922080 GTGGAACTAGAGAATAGGAAAGACATGAACCAACGCCCAAAATGAGAAAGAAGGACATATAAAGA GTGGAACTAGAGAATAGGAAAGACATGAACCAGCGCCCAAAATGAGAAAGAAGGACATATAAAGA A G AL031591.1,TTC28-AS1 Ensembl:ENSG00000276150,Ensembl:ENSG00000235954 Other,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:27922019..27922128 26863196 MeRIP-seq:(Medium) rs970916848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931407,Human_RBP_ID_1614274,Human_RBP_ID_3679096,Human_RBP_ID_4690283,Human_RBP_ID_5101595,Human_RBP_ID_5600678,Human_RBP_ID_14432759 Human_Splice_Rec_2149136,Human_Splice_Rec_2149198,Human_Splice_Rec_2149199,Human_Splice_Rec_2149216,Human_Splice_Rec_2149250,Human_Splice_Rec_2149252,Human_Splice_Rec_2149253,Human_Splice_Rec_2149258,Human_Splice_Rec_2149262,Human_Splice_Rec_2149282,Human_Splice_Rec_2149286,Human_Splice_Rec_2149287,Human_Splice_Rec_2149294,Human_Splice_Rec_2149295 RMVar_hsa_circ_84497,RMVar_hsa_circ_213518 89908 RMVar_ID_89908 Human_SNP_ID_701138744 m1A Human chr22 - 28461833 28461833 28461833 GGGGTTAGCATGACTGGTGGGAAAGACAGAGAAGAGAGCACAATGTATGGAGTAAGGTGGCCTTA GGGGTTAGCATGACTGGTGGGAAAGACAGAGAGGAGAGCACAATGTATGGAGTAAGGTGGCCTTA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:28461724..28462004;chr22:28461725..28461991 26863196 MeRIP-seq:(Medium) rs114182048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94269,RMVar_hsa_circ_213520,RMVar_hsa_circ_77115,RMVar_hsa_circ_213522,RMVar_hsa_circ_85659,RMVar_hsa_circ_213525,RMVar_hsa_circ_213527,RMVar_hsa_circ_111444,RMVar_hsa_circ_213528,RMVar_hsa_circ_80323,RMVar_hsa_circ_97822,RMVar_hsa_circ_213536,RMVar_hsa_circ_106306,RMVar_hsa_circ_87353,RMVar_hsa_circ_213540,RMVar_hsa_circ_97751,RMVar_hsa_circ_213542,RMVar_hsa_circ_213546,RMVar_hsa_circ_90048,RMVar_hsa_circ_213547 89909 RMVar_ID_89909 Human_SNP_ID_701161755 m1A Human chr22 - 28559640 28559640 28559640 TGTGTCAAATACTAAGATTATGTCCTGAAGAAAGACCACTTTGGTTATAGGATGGATGATGGACT TGTGTCAAATACTAAGATTATGTCCTGAAGAAGGACCACTTTGGTTATAGGATGGATGATGGACT T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28559593..28559676 26863196 MeRIP-seq:(Medium) rs1354801182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8547716 RMVar_hsa_circ_94269,RMVar_hsa_circ_213520,RMVar_hsa_circ_77115,RMVar_hsa_circ_213522,RMVar_hsa_circ_85659,RMVar_hsa_circ_213525,RMVar_hsa_circ_213527,RMVar_hsa_circ_111444,RMVar_hsa_circ_213528,RMVar_hsa_circ_80323,RMVar_hsa_circ_97822,RMVar_hsa_circ_213536,RMVar_hsa_circ_106306,RMVar_hsa_circ_87353,RMVar_hsa_circ_213540,RMVar_hsa_circ_97751,RMVar_hsa_circ_213542,RMVar_hsa_circ_213546,RMVar_hsa_circ_90048,RMVar_hsa_circ_213547,RMVar_hsa_circ_213559 89910 RMVar_ID_89910 Human_SNP_ID_701161778 m1A Human chr22 - 28559799 28559799 28559799 GAAGACTGAGGACTGAGTCTTGTGGCACTTCAACATTCAGAATTTAGGAAAAGATGGGAATATCA GAAGACTGAGGACTGAGTCTTGTGGCACTTCAGCATTCAGAATTTAGGAAAAGATGGGAATATCA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28559754..28559875 26863196 MeRIP-seq:(Medium) rs996520668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2715149,Human_RBP_ID_14437710 RMVar_hsa_circ_94269,RMVar_hsa_circ_213520,RMVar_hsa_circ_77115,RMVar_hsa_circ_213522,RMVar_hsa_circ_85659,RMVar_hsa_circ_213525,RMVar_hsa_circ_213527,RMVar_hsa_circ_111444,RMVar_hsa_circ_213528,RMVar_hsa_circ_80323,RMVar_hsa_circ_97822,RMVar_hsa_circ_213536,RMVar_hsa_circ_106306,RMVar_hsa_circ_87353,RMVar_hsa_circ_213540,RMVar_hsa_circ_97751,RMVar_hsa_circ_213542,RMVar_hsa_circ_213546,RMVar_hsa_circ_90048,RMVar_hsa_circ_213547,RMVar_hsa_circ_213559 89911 RMVar_ID_89911 Human_SNP_ID_701161914 m1A Human chr22 - 28560544 28560544 28560544 AGTTCCTTGGGTGGGAATGATTATGTATGGGAAAAACTGCAGAAAGTTTGTGAGTGTGAAGAGAG AGTTCCTTGGGTGGGAATGATTATGTATGGGAGAAACTGCAGAAAGTTTGTGAGTGTGAAGAGAG T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28560493..28560609 26863196 MeRIP-seq:(Medium) rs1269680242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94269,RMVar_hsa_circ_213520,RMVar_hsa_circ_77115,RMVar_hsa_circ_213522,RMVar_hsa_circ_85659,RMVar_hsa_circ_213525,RMVar_hsa_circ_213527,RMVar_hsa_circ_111444,RMVar_hsa_circ_213528,RMVar_hsa_circ_80323,RMVar_hsa_circ_97822,RMVar_hsa_circ_213536,RMVar_hsa_circ_106306,RMVar_hsa_circ_87353,RMVar_hsa_circ_213540,RMVar_hsa_circ_97751,RMVar_hsa_circ_213542,RMVar_hsa_circ_213546,RMVar_hsa_circ_90048,RMVar_hsa_circ_213547,RMVar_hsa_circ_213559 89912 RMVar_ID_89912 Human_SNP_ID_701205228 m1A Human chr22 - 28734690 28734690 28734690 GATGTCTCGGGAGTCGGATGTTGAGGCTCAGCAGTCTCATGGCAGCAGTGCCTGTTCACAGCCCC GATGTCTCGGGAGTCGGATGTTGAGGCTCAGCGGTCTCATGGCAGCAGTGCCTGTTCACAGCCCC T C CHEK2 Ensembl:ENSG00000183765 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28734640..28734705 26863196 MeRIP-seq:(Medium) rs369256181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708531 Human_Splice_Rec_2149484,Human_Splice_Rec_2149512,Human_Splice_Rec_2149538,Human_Splice_Rec_2149614,Human_Splice_Rec_2149642,Human_Splice_Rec_2149674,Human_Splice_Rec_2149836,Human_Splice_Rec_2149898,Human_Splice_Rec_2149910,Human_Splice_Rec_2149926,Human_Splice_Rec_2149936 Clinvar_Rec_507 RMVar_hsa_circ_38531,RMVar_hsa_circ_43099,RMVar_hsa_circ_350199,RMVar_hsa_circ_281135,RMVar_hsa_circ_213571,RMVar_hsa_circ_289414,RMVar_hsa_circ_213570,RMVar_hsa_circ_295467,RMVar_hsa_circ_334440,RMVar_hsa_circ_274356,RMVar_hsa_circ_326919,RMVar_hsa_circ_213572,RMVar_hsa_circ_329307,RMVar_hsa_circ_48756,RMVar_hsa_circ_213573,RMVar_hsa_circ_213575,RMVar_hsa_circ_295129 89913 RMVar_ID_89913 Human_SNP_ID_701205229 m1A Human chr22 - 28734690 28734690 28734690 GATGTCTCGGGAGTCGGATGTTGAGGCTCAGCAGTCTCATGGCAGCAGTGCCTGTTCACAGCCCC GATGTCTCGGGAGTCGGATGTTGAGGCTCAGCCGTCTCATGGCAGCAGTGCCTGTTCACAGCCCC T G CHEK2 Ensembl:ENSG00000183765 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28734640..28734705 26863196 MeRIP-seq:(Medium) rs369256181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708531 Human_Splice_Rec_2149484,Human_Splice_Rec_2149512,Human_Splice_Rec_2149538,Human_Splice_Rec_2149614,Human_Splice_Rec_2149642,Human_Splice_Rec_2149674,Human_Splice_Rec_2149836,Human_Splice_Rec_2149898,Human_Splice_Rec_2149910,Human_Splice_Rec_2149926,Human_Splice_Rec_2149936 Clinvar_Rec_507 RMVar_hsa_circ_38531,RMVar_hsa_circ_43099,RMVar_hsa_circ_350199,RMVar_hsa_circ_281135,RMVar_hsa_circ_213571,RMVar_hsa_circ_289414,RMVar_hsa_circ_213570,RMVar_hsa_circ_295467,RMVar_hsa_circ_334440,RMVar_hsa_circ_274356,RMVar_hsa_circ_326919,RMVar_hsa_circ_213572,RMVar_hsa_circ_329307,RMVar_hsa_circ_48756,RMVar_hsa_circ_213573,RMVar_hsa_circ_213575,RMVar_hsa_circ_295129 89914 RMVar_ID_89914 Human_SNP_ID_701207233 m1A Human chr22 - 28742130 28742130 28742130 TTCTGGGAACCCCTGTCGGCCAAAACCCCCACACCCGGAGCAAAGCCCCGGCTCTCCCCCGCCAC TTCTGGGAACCCCTGTCGGCCAAAACCCCCACCCCCGGAGCAAAGCCCCGGCTCTCCCCCGCCAC T G CHEK2 Ensembl:ENSG00000183765 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28742079..28742238 26863196 MeRIP-seq:(Medium) rs751442241 Functional Loss SNV dbSNP153 33..33 33 - - - 89915 RMVar_ID_89915 Human_SNP_ID_701215879 m1A Human chr22 - 28772749 28772749 28772749 CCACAGCTACTGCCAAAACCCGCCAGCCTCGGATCCCGCTCTCGACCCCACGTCACGCCTTCTAG CCACAGCTACTGCCAAAACCCGCCAGCCTCGGGTCCCGCTCTCGACCCCACGTCACGCCTTCTAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:28772701..28772856 26863196 MeRIP-seq:(Medium) rs934260442 Functional Loss SNV dbSNP153 33..33 33 - - - 89916 RMVar_ID_89916 Human_SNP_ID_701215889 m1A Human chr22 - 28772767 28772767 28772767 CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCAAAACCCGCCAGCCTCGGATCCCGCTCTCGACC CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCGAAACCCGCCAGCCTCGGATCCCGCTCTCGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28772717..28772842 26863196 MeRIP-seq:(Medium) rs11556025 Functional Loss SNV dbSNP153 33..33 33 - - - 89917 RMVar_ID_89917 Human_SNP_ID_701215890 m1A Human chr22 - 28772767 28772767 28772767 CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCAAAACCCGCCAGCCTCGGATCCCGCTCTCGACC CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCCAAACCCGCCAGCCTCGGATCCCGCTCTCGACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28772717..28772842 26863196 MeRIP-seq:(Medium) rs11556025 Functional Loss SNV dbSNP153 33..33 33 - - - 89918 RMVar_ID_89918 Human_SNP_ID_701215894 m1A Human chr22 + 28772774 28772774 28772774 AGCGGGATCCGAGGCTGGCGGGTTTTGGCAGTAGCTGTGGCTGCGGCTGCCGGGCCTGGGGACGC AGCGGGATCCGAGGCTGGCGGGTTTTGGCAGTCGCTGTGGCTGCGGCTGCCGGGCCTGGGGACGC A C CCDC117 Ensembl:ENSG00000159873 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:28772727..28772843 26863196 MeRIP-seq:(Medium) rs761842252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246194,Human_RBP_ID_577379,Human_RBP_ID_781570,Human_RBP_ID_834246,Human_RBP_ID_4690567,Human_RBP_ID_5446357,Human_RBP_ID_5472933,Human_RBP_ID_5530100,Human_RBP_ID_7071600,Human_RBP_ID_8862210,Human_RBP_ID_18423624,Human_RBP_ID_22454872 RMVar_hsa_circ_122956,RMVar_hsa_circ_213578 89919 RMVar_ID_89919 Human_SNP_ID_701215895 m1A Human chr22 + 28772774 28772774 28772774 AGCGGGATCCGAGGCTGGCGGGTTTTGGCAGTAGCTGTGGCTGCGGCTGCCGGGCCTGGGGACGC AGCGGGATCCGAGGCTGGCGGGTTTTGGCAGTTGCTGTGGCTGCGGCTGCCGGGCCTGGGGACGC A T CCDC117 Ensembl:ENSG00000159873 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:28772727..28772843 26863196 MeRIP-seq:(Medium) rs761842252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246194,Human_RBP_ID_577379,Human_RBP_ID_781570,Human_RBP_ID_834246,Human_RBP_ID_4690567,Human_RBP_ID_5446357,Human_RBP_ID_5472933,Human_RBP_ID_5530100,Human_RBP_ID_7071600,Human_RBP_ID_8862210,Human_RBP_ID_18423624,Human_RBP_ID_22454872 RMVar_hsa_circ_122956,RMVar_hsa_circ_213578 89920 RMVar_ID_89920 Human_SNP_ID_701223017 m1A Human chr22 - 28797090 28797090 28797090 CTTGGGGATGGATGCCCTGGTTGCTGAAGAGGAGGCGGAAGCCAAGGTAAATCATCTCCTTTATT CTTGGGGATGGATGCCCTGGTTGCTGAAGAGGCGGCGGAAGCCAAGGTAAATCATCTCCTTTATT T G XBP1 Ensembl:ENSG00000100219 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:28797076..28797150 26863196 MeRIP-seq:(Medium) rs148722004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245858,Human_RBP_ID_781223,Human_RBP_ID_833371,Human_RBP_ID_932392,Human_RBP_ID_5149315,Human_RBP_ID_8547850,Human_RBP_ID_9260677,Human_RBP_ID_9300320,Human_RBP_ID_19111783 Human_Splice_Rec_2150047,Human_Splice_Rec_2150055,Human_Splice_Rec_2150065,Human_Splice_Rec_2150073,Human_Splice_Rec_2150081 RMVar_hsa_circ_110299,RMVar_hsa_circ_120339,RMVar_hsa_circ_213583,RMVar_hsa_circ_100890,RMVar_hsa_circ_213581,RMVar_hsa_circ_213582,RMVar_hsa_circ_64989,RMVar_hsa_circ_354892 89921 RMVar_ID_89921 Human_SNP_ID_701223607 m1A Human chr22 - 28799155 28799155 28799155 ATGACTCAGTGTGGTATGTTCCTTCTCTTCCTAGGAAACTGAAAAACAGAGTAGCAGCTCAGACT ATGACTCAGTGTGGTATGTTCCTTCTCTTCCTGGGAAACTGAAAAACAGAGTAGCAGCTCAGACT T C XBP1 Ensembl:ENSG00000100219 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:28799126..28799175 26863196 MeRIP-seq:(Medium) rs906958955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_932394,Human_RBP_ID_19111785 Human_Splice_Rec_2150045,Human_Splice_Rec_2150063,Human_Splice_Rec_2150071,Human_Splice_Rec_2150079 RMVar_hsa_circ_100890,RMVar_hsa_circ_213581 89922 RMVar_ID_89922 Human_SNP_ID_701223987 m1A Human chr22 - 28800346 28800346 28800346 GGCAGCGAGCGGGGGGCTGCCCCAGGCGCGCAAGCGACAGCGCCTCACGCACCTGAGCCCCGAGG GGCAGCGAGCGGGGGGCTGCCCCAGGCGCGCAGGCGACAGCGCCTCACGCACCTGAGCCCCGAGG T C XBP1 Ensembl:ENSG00000100219 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:28800301..28800455 26863196 MeRIP-seq:(Medium) rs1472775618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245861,Human_RBP_ID_4690749,Human_RBP_ID_5149177,Human_RBP_ID_8865912 Human_Splice_Rec_2150043,Human_Splice_Rec_2150051,Human_Splice_Rec_2150061,Human_Splice_Rec_2150077,Human_Splice_Rec_2150085 RMVar_hsa_circ_100890,RMVar_hsa_circ_213581 89923 RMVar_ID_89923 Human_SNP_ID_701224019 m1A Human chr22 + 28800418 28800418 28800418 TGGCCCCTCTCTGGGCTGGCACCATGAGCGGCAGGGCCTGGCCGGCCGGGGCTCCGGCGGCGGAG TGGCCCCTCTCTGGGCTGGCACCATGAGCGGCGGGGCCTGGCCGGCCGGGGCTCCGGCGGCGGAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:28800301..28800550 26863410 MeRIP-seq:(Medium) rs1243420527 Functional Loss SNV dbSNP153 33..33 33 - - - 89924 RMVar_ID_89924 Human_SNP_ID_701224079 m1A Human chr22 - 28800510 28800510 28800510 GGTGCGTAGTCTGGAGCTATGGTGGTGGTGGCAGCCGCGCCGAACCCGGCCGACGGGACCCCTAA GGTGCGTAGTCTGGAGCTATGGTGGTGGTGGCGGCCGCGCCGAACCCGGCCGACGGGACCCCTAA T C XBP1 Ensembl:ENSG00000100219 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:28800159..28800575 26863196 MeRIP-seq:(Medium) rs939447877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245861,Human_RBP_ID_833374,Human_RBP_ID_932398,Human_RBP_ID_1028835,Human_RBP_ID_4690751,Human_RBP_ID_5149322,Human_RBP_ID_5324162,Human_RBP_ID_5472938,Human_RBP_ID_8862315,Human_RBP_ID_17701753,Human_RBP_ID_23941488 RMVar_hsa_circ_100890,RMVar_hsa_circ_213581 89925 RMVar_ID_89925 Human_SNP_ID_701231374 m1A Human chr22 + 28831231 28831211 28831232 TGGTGTCTCTGCAGTGGGTGCTGTTGTCTCTGAGGTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG TGGTGTCTCTGCA_____________________GTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG AGTGGGTGCTGTTGTCTCTGAG A Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28831180..28831283 26863196 MeRIP-seq:(Medium) rs1442467282 Functional Loss DEL dbSNP153 14..34 33 - - - 89926 RMVar_ID_89926 Human_SNP_ID_701231380 m1A Human chr22 + 28831231 28831229 28831231 TGGTGTCTCTGCAGTGGGTGCTGTTGTCTCTGAGGTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG TGGTGTCTCTGCAGTGGGTGCTGTTGTCTCT__GGTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG TGA T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28831180..28831283 26863196 MeRIP-seq:(Medium) rs1394613460 Functional Loss DEL dbSNP153 32..33 33 - - - 89927 RMVar_ID_89927 Human_SNP_ID_701231381 m1A Human chr22 + 28831231 28831231 28831231 TGGTGTCTCTGCAGTGGGTGCTGTTGTCTCTGAGGTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG TGGTGTCTCTGCAGTGGGTGCTGTTGTCTCTGTGGTGGGTGCTGTTGTCTCTGTGGTGGGTGTTG A T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28831180..28831283 26863196 MeRIP-seq:(Medium) rs1166961721 Functional Loss SNV dbSNP153 33..33 33 - - - 89928 RMVar_ID_89928 Human_SNP_ID_701231450 m1A Human chr22 + 28831492 28831492 28831492 TGGTGTCTCTGTGGTGGGTGTTGTTGTGTCTGAGGTGGGTGTTGGTGTCTCTGAGGTGCGTGTTG TGGTGTCTCTGTGGTGGGTGTTGTTGTGTCTGGGGTGGGTGTTGGTGTCTCTGAGGTGCGTGTTG A G Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:28831457..28831693 26863196 MeRIP-seq:(Medium) rs1292416079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23941500 89929 RMVar_ID_89929 Human_SNP_ID_701231451 m1A Human chr22 + 28831492 28831492 28831492 TGGTGTCTCTGTGGTGGGTGTTGTTGTGTCTGAGGTGGGTGTTGGTGTCTCTGAGGTGCGTGTTG TGGTGTCTCTGTGGTGGGTGTTGTTGTGTCTGTGGTGGGTGTTGGTGTCTCTGAGGTGCGTGTTG A T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:28831457..28831693 26863196 MeRIP-seq:(Medium) rs1292416079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23941500 89930 RMVar_ID_89930 Human_SNP_ID_701259644 m1A Human chr22 + 28946767 28946767 28946767 GAGGGTGTTCTGGGGACTGGGGAGTGGGTTTCATTTGTGTTTGGCAGTAGCTGGTGATGGCTGTT GAGGGTGTTCTGGGGACTGGGGAGTGGGTTTCCTTTGTGTTTGGCAGTAGCTGGTGATGGCTGTT A C ZNRF3 Ensembl:ENSG00000183579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28946761..28946844 26863196 MeRIP-seq:(Medium) rs537481692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17147471,Human_RBP_ID_23286146,Human_RBP_ID_24381231 89931 RMVar_ID_89931 Human_SNP_ID_701259645 m1A Human chr22 + 28946767 28946767 28946767 GAGGGTGTTCTGGGGACTGGGGAGTGGGTTTCATTTGTGTTTGGCAGTAGCTGGTGATGGCTGTT GAGGGTGTTCTGGGGACTGGGGAGTGGGTTTCGTTTGTGTTTGGCAGTAGCTGGTGATGGCTGTT A G ZNRF3 Ensembl:ENSG00000183579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28946761..28946844 26863196 MeRIP-seq:(Medium) rs537481692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17147471,Human_RBP_ID_23286146,Human_RBP_ID_24381231 89932 RMVar_ID_89932 Human_SNP_ID_701264773 m1A Human chr22 - 28969469 28969469 28969469 CTGCCTGGAATAATCTACCCTCACTAGGCTTGACTCTGTCCTTAACCTCCTTTACATATCACCTT CTGCCTGGAATAATCTACCCTCACTAGGCTTGTCTCTGTCCTTAACCTCCTTTACATATCACCTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28969463..28969610 26863196 MeRIP-seq:(Medium) rs1288500613 Functional Loss SNV dbSNP153 33..33 33 - - - 89933 RMVar_ID_89933 Human_SNP_ID_701275845 m1A Human chr22 + 29018555 29018555 29018555 AGAAGTCATTAGATAGGGGAGTGTGTATTCAAACCAGGAGTCCAGAATGAGCTTGTCCAGAAAAG AGAAGTCATTAGATAGGGGAGTGTGTATTCAAGCCAGGAGTCCAGAATGAGCTTGTCCAGAAAAG A G ZNRF3-IT1,ZNRF3 Ensembl:ENSG00000235786,Ensembl:ENSG00000183579 lincRNA,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29018549..29018850 26863196 MeRIP-seq:(Medium) rs1429444878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30782 89934 RMVar_ID_89934 Human_SNP_ID_701283550 m1A Human chr22 - 29050060 29050060 29050060 GTGCACCGCCGGGAGCTCCTCGGGAGGCGGGGAGCCCTCGAAGCACAGGGCAGGTCCCCGGCCCG GTGCACCGCCGGGAGCTCCTCGGGAGGCGGGGGGCCCTCGAAGCACAGGGCAGGTCCCCGGCCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:29050009..29050165 26863196 MeRIP-seq:(Medium) rs1319175456 Functional Loss SNV dbSNP153 33..33 33 - - - 89935 RMVar_ID_89935 Human_SNP_ID_701290073 m1A Human chr22 - 29073092 29073092 29073092 TCAGTGCGGGGCCCCGGGGCGCGGCCCGGGGTAAAGGGGGCAGCGCGGGGAGCCGGGGGCGGCCA TCAGTGCGGGGCCCCGGGGCGCGGCCCGGGGTGAAGGGGGCAGCGCGGGGAGCCGGGGGCGGCCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:29073066..29073214 26863196 MeRIP-seq:(Medium) rs1193292947 Functional Loss SNV dbSNP153 33..33 33 - - - 89936 RMVar_ID_89936 Human_SNP_ID_701290104 m1A Human chr22 + 29073142 29073142 29073142 GGGGCCCCGCACTGACGGCCCATGGCGCCGCCAGCCGCCCGCCTCGCCCTGCTCTCCGCCGCGGC GGGGCCCCGCACTGACGGCCCATGGCGCCGCCCGCCGCCCGCCTCGCCCTGCTCTCCGCCGCGGC A C KREMEN1 Ensembl:ENSG00000183762 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr22:29073026..29073175;chr22:29073026..29073200;chr22:29073096..29073163 26863410,26863196 MeRIP-seq:(Medium) rs7292708 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_931843,Human_RBP_ID_4708927 Human_Splice_Rec_2150155,Human_Splice_Rec_2150171 GWAS_ID_11662,GWAS_ID_11663,GWAS_ID_11664,GWAS_ID_11665,GWAS_ID_11666,GWAS_ID_11667,GWAS_ID_11668,GWAS_ID_11669,GWAS_ID_11670,GWAS_ID_11671,GWAS_ID_11672,GWAS_ID_11673,GWAS_ID_11674,GWAS_ID_11675,GWAS_ID_11676,GWAS_ID_11677,GWAS_ID_11678,GWAS_ID_11679,GWAS_ID_11680,GWAS_ID_11681,GWAS_ID_11682,GWAS_ID_11683,GWAS_ID_11684,GWAS_ID_11685,GWAS_ID_11686,GWAS_ID_11687,GWAS_ID_11688 RMVar_hsa_circ_213593,RMVar_hsa_circ_83202 89937 RMVar_ID_89937 Human_SNP_ID_701300553 m1A Human chr22 + 29120334 29120333 29120335 GAAACAGGGAGGAGGGAGAGGTGATGATGGAAACAGGGAGGAGGGAGAGGTGATGAAGGAAATGG GAAACAGGGAGGAGGGAGAGGTGATGATGGAA__AGGGAGGAGGGAGAGGTGATGAAGGAAATGG AAC A KREMEN1 Ensembl:ENSG00000183762 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29120332..29120696 26863196 MeRIP-seq:(Medium) rs1174655322 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_44914,RMVar_hsa_circ_213593,RMVar_hsa_circ_83202,RMVar_hsa_circ_301357,RMVar_hsa_circ_30841,RMVar_hsa_circ_213594 89938 RMVar_ID_89938 Human_SNP_ID_701321289 m1A Human chr22 - 29206069 29206069 29206069 AGCGCCGCCTCCCGGGAGCAGGAGCCCGAGGCAGAGCAGCGCCCAAGCCCGCGGGCCGCCCATGC AGCGCCGCCTCCCGGGAGCAGGAGCCCGAGGCTGAGCAGCGCCCAAGCCCGCGGGCCGCCCATGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29205958..29206114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89939 RMVar_ID_89939 Human_SNP_ID_701321290 m1A Human chr22 - 29206069 29206069 29206069 AGCGCCGCCTCCCGGGAGCAGGAGCCCGAGGCAGAGCAGCGCCCAAGCCCGCGGGCCGCCCATGC AGCGCCGCCTCCCGGGAGCAGGAGCCCGAGGCGGAGCAGCGCCCAAGCCCGCGGGCCGCCCATGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29205958..29206114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89940 RMVar_ID_89940 Human_SNP_ID_701337656 m1A Human chr22 + 29268335 29268335 29268335 CGGACGTTGAGAGAACGAGGAGGAAGGAGAGAAAATGGCGTCCACGGGTGAGTATGGTGGAACTG CGGACGTTGAGAGAACGAGGAGGAAGGAGAGAGAATGGCGTCCACGGGTGAGTATGGTGGAACTG A G EWSR1 Ensembl:ENSG00000182944 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29268276..29268417 26863196 MeRIP-seq:(Medium) rs1401933662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246213,Human_RBP_ID_781624,Human_RBP_ID_833964,Human_RBP_ID_1609588,Human_RBP_ID_1941263,Human_RBP_ID_5504503,Human_RBP_ID_8865916,Human_RBP_ID_9392099,Human_RBP_ID_18786671,Human_RBP_ID_19111799,Human_RBP_ID_23115706,Human_RBP_ID_26345262,Human_RBP_ID_26822997 Human_Splice_Rec_2150433,Human_Splice_Rec_2150441,Human_Splice_Rec_2150473,Human_Splice_Rec_2150501,Human_Splice_Rec_2150533,Human_Splice_Rec_2150545,Human_Splice_Rec_2150557,Human_Splice_Rec_2150565,Human_Splice_Rec_2150597,Human_Splice_Rec_2150611,Human_Splice_Rec_2150621,Human_Splice_Rec_2150649,Human_Splice_Rec_2150663,Human_Splice_Rec_2150697,Human_Splice_Rec_2150713,Human_Splice_Rec_2150725 RMVar_hsa_circ_79570,RMVar_hsa_circ_104959,RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_213606,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_213607 89941 RMVar_ID_89941 Human_SNP_ID_701337659 m1A Human chr22 + 29268346 29268346 29268346 AGAACGAGGAGGAAGGAGAGAAAATGGCGTCCACGGGTGAGTATGGTGGAACTGCGGTCGCGCCG AGAACGAGGAGGAAGGAGAGAAAATGGCGTCCCCGGGTGAGTATGGTGGAACTGCGGTCGCGCCG A C EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:29268321..29268461 26863196 MeRIP-seq:(Medium) rs761661070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833964,Human_RBP_ID_5504503,Human_RBP_ID_9392099,Human_RBP_ID_19111799,Human_RBP_ID_23115706,Human_RBP_ID_26345262,Human_RBP_ID_26822997 Human_Splice_Rec_2150433,Human_Splice_Rec_2150441,Human_Splice_Rec_2150473,Human_Splice_Rec_2150501,Human_Splice_Rec_2150533,Human_Splice_Rec_2150545,Human_Splice_Rec_2150557,Human_Splice_Rec_2150565,Human_Splice_Rec_2150597,Human_Splice_Rec_2150611,Human_Splice_Rec_2150621,Human_Splice_Rec_2150649,Human_Splice_Rec_2150663,Human_Splice_Rec_2150697,Human_Splice_Rec_2150713,Human_Splice_Rec_2150725 RMVar_hsa_circ_79570,RMVar_hsa_circ_104959,RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_213606,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_213607 89942 RMVar_ID_89942 Human_SNP_ID_701337660 m1A Human chr22 + 29268346 29268346 29268346 AGAACGAGGAGGAAGGAGAGAAAATGGCGTCCACGGGTGAGTATGGTGGAACTGCGGTCGCGCCG AGAACGAGGAGGAAGGAGAGAAAATGGCGTCCGCGGGTGAGTATGGTGGAACTGCGGTCGCGCCG A G EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:29268321..29268461 26863196 MeRIP-seq:(Medium) rs761661070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833964,Human_RBP_ID_5504503,Human_RBP_ID_9392099,Human_RBP_ID_19111799,Human_RBP_ID_23115706,Human_RBP_ID_26345262,Human_RBP_ID_26822997 Human_Splice_Rec_2150433,Human_Splice_Rec_2150441,Human_Splice_Rec_2150473,Human_Splice_Rec_2150501,Human_Splice_Rec_2150533,Human_Splice_Rec_2150545,Human_Splice_Rec_2150557,Human_Splice_Rec_2150565,Human_Splice_Rec_2150597,Human_Splice_Rec_2150611,Human_Splice_Rec_2150621,Human_Splice_Rec_2150649,Human_Splice_Rec_2150663,Human_Splice_Rec_2150697,Human_Splice_Rec_2150713,Human_Splice_Rec_2150725 RMVar_hsa_circ_79570,RMVar_hsa_circ_104959,RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_213606,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_213607 89943 RMVar_ID_89943 Human_SNP_ID_701339029 m1A Human chr22 - 29272203 29272192 29272204 TTGGCTATAGGTACTGTAATCTAGAGGAAAACAAGGAGGAAAAATAGTGTAAAGTTAGCAGAAAC TTGGCTATAGGTACTGTAATCTAGAGGAAAA____________ATAGTGTAAAGTTAGCAGAAAC TTTTTCCTCCTTG T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:29272201..29272275;chr22:29272201..29272450 26863196 MeRIP-seq:(Medium) rs1286252469 Functional Loss DEL dbSNP153 32..43 33 - - - 89944 RMVar_ID_89944 Human_SNP_ID_701339035 m1A Human chr22 - 29272213 29272201 29272213 GCGCTGCAGCTTGGCTATAGGTACTGTAATCTAGAGGAAAACAAGGAGGAAAAATAGTGTAAAGT GCGCTGCAGCTTGGCTATAGGTACTGTAATCT____________GGAGGAAAAATAGTGTAAAGT CTTGTTTTCCTCT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:29272201..29272275 26863410 MeRIP-seq:(Medium) rs1188836320 Functional Loss DEL dbSNP153 33..44 33 - - - 89945 RMVar_ID_89945 Human_SNP_ID_701339036 m1A Human chr22 - 29272203 29272203 29272203 TTGGCTATAGGTACTGTAATCTAGAGGAAAACAAGGAGGAAAAATAGTGTAAAGTTAGCAGAAAC TTGGCTATAGGTACTGTAATCTAGAGGAAAACGAGGAGGAAAAATAGTGTAAAGTTAGCAGAAAC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:29272201..29272275;chr22:29272201..29272450 26863196 MeRIP-seq:(Medium) rs368813757 Functional Loss SNV dbSNP153 33..33 33 - - - 89946 RMVar_ID_89946 Human_SNP_ID_701339037 m1A Human chr22 - 29272203 29272203 29272203 TTGGCTATAGGTACTGTAATCTAGAGGAAAACAAGGAGGAAAAATAGTGTAAAGTTAGCAGAAAC TTGGCTATAGGTACTGTAATCTAGAGGAAAACCAGGAGGAAAAATAGTGTAAAGTTAGCAGAAAC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:29272201..29272275;chr22:29272201..29272450 26863196 MeRIP-seq:(Medium) rs368813757 Functional Loss SNV dbSNP153 33..33 33 - - - 89947 RMVar_ID_89947 Human_SNP_ID_701339050 m1A Human chr22 + 29272241 29272241 29272241 CCTCTAGATTACAGTACCTATAGCCAAGCTGCAGCGCAGCAGGGGTAAGTCAGTCTTTTATAACC CCTCTAGATTACAGTACCTATAGCCAAGCTGCTGCGCAGCAGGGGTAAGTCAGTCTTTTATAACC A T EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:29272232..29273816 32194978 MeRIP-seq:(Medium) rs1309659035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833751,Human_RBP_ID_932618,Human_RBP_ID_5119706,Human_RBP_ID_5324748,Human_RBP_ID_5387740,Human_RBP_ID_19111800,Human_RBP_ID_22454395,Human_RBP_ID_22674219,Human_RBP_ID_24561091,Human_RBP_ID_25680408 Human_Splice_Rec_2150434,Human_Splice_Rec_2150435,Human_Splice_Rec_2150442,Human_Splice_Rec_2150443,Human_Splice_Rec_2150474,Human_Splice_Rec_2150475,Human_Splice_Rec_2150502,Human_Splice_Rec_2150503,Human_Splice_Rec_2150534,Human_Splice_Rec_2150535,Human_Splice_Rec_2150546,Human_Splice_Rec_2150547,Human_Splice_Rec_2150558,Human_Splice_Rec_2150559,Human_Splice_Rec_2150566,Human_Splice_Rec_2150567,Human_Splice_Rec_2150598,Human_Splice_Rec_2150599,Human_Splice_Rec_2150612,Human_Splice_Rec_2150613,Human_Splice_Rec_2150622,Human_Splice_Rec_2150623,Human_Splice_Rec_2150650,Human_Splice_Rec_2150651,Human_Splice_Rec_2150664,Human_Splice_Rec_2150665,Human_Splice_Rec_2150698,Human_Splice_Rec_2150699,Human_Splice_Rec_2150714,Human_Splice_Rec_2150715,Human_Splice_Rec_2150726,Human_Splice_Rec_2150727,Human_Splice_Rec_2150756,Human_Splice_Rec_2150757 Human_miRNA_ID_2014266,Human_miRNA_ID_2513483,Human_miRNA_ID_2760665,Human_miRNA_ID_3056304 RMVar_hsa_circ_79570,RMVar_hsa_circ_104959,RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_96308,RMVar_hsa_circ_213606,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_213607,RMVar_hsa_circ_105688,RMVar_hsa_circ_213610,RMVar_hsa_circ_213611 89948 RMVar_ID_89948 Human_SNP_ID_701339065 m1A Human chr22 - 29272290 29272290 29272290 AATTATAGAAGGCTCCATATTCAAAAAATATTAATCACACACAAAATACGGTTATAAAAGACTGA AATTATAGAAGGCTCCATATTCAAAAAATATTTATCACACACAAAATACGGTTATAAAAGACTGA T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:29272288..29272411 26863196 MeRIP-seq:(Medium) rs199543598 Functional Loss SNV dbSNP153 33..33 33 - - - 89949 RMVar_ID_89949 Human_SNP_ID_701339066 m1A Human chr22 - 29272290 29272290 29272290 AATTATAGAAGGCTCCATATTCAAAAAATATTAATCACACACAAAATACGGTTATAAAAGACTGA AATTATAGAAGGCTCCATATTCAAAAAATATTCATCACACACAAAATACGGTTATAAAAGACTGA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:29272288..29272411 26863196 MeRIP-seq:(Medium) rs199543598 Functional Loss SNV dbSNP153 33..33 33 - - - 89950 RMVar_ID_89950 Human_SNP_ID_701340801 m1A Human chr22 - 29278172 29278172 29278172 GTGGCTGCTGGCTGCTGCCCATAGGCTGGATAAGCAGGCTGAGTGCCATATGCAGACTGAGCTGC GTGGCTGCTGGCTGCTGCCCATAGGCTGGATAGGCAGGCTGAGTGCCATATGCAGACTGAGCTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:29278083..29288642 32194978 MeRIP-seq:(Medium) rs776204033 Functional Loss SNV dbSNP153 33..33 33 - - - 89951 RMVar_ID_89951 Human_SNP_ID_701342298 m1A Human chr22 - 29282541 29282541 29282541 CAAAAAGTAGACTGACCTGGTAGGAGGGTAGGATGGAGGTGCAGTGACTGGCTGCATGGGGTAGC CAAAAAGTAGACTGACCTGGTAGGAGGGTAGGCTGGAGGTGCAGTGACTGGCTGCATGGGGTAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29282491..29282597 26863196 MeRIP-seq:(Medium) rs776957366 Functional Loss SNV dbSNP153 33..33 33 - - - 89952 RMVar_ID_89952 Human_SNP_ID_701343727 m1A Human chr22 + 29287029 29287029 29287029 GCTATGGACAGCAGAGTAGCTATGGTCAACAAAGCAGCTATGGGCAGCAGCCTCCCACTAGTTAC GCTATGGACAGCAGAGTAGCTATGGTCAACAAGGCAGCTATGGGCAGCAGCCTCCCACTAGTTAC A G EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29286979..29287076 26863196 MeRIP-seq:(Medium) rs373486719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833970,Human_RBP_ID_7095170,Human_RBP_ID_14444479,Human_RBP_ID_17399775,Human_RBP_ID_22820006,Human_RBP_ID_23941918,Human_RBP_ID_27034839 Human_miRNA_ID_2716740 RMVar_hsa_circ_26597,RMVar_hsa_circ_113042,RMVar_hsa_circ_213609,RMVar_hsa_circ_115792,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_325413,RMVar_hsa_circ_312881,RMVar_hsa_circ_42395,RMVar_hsa_circ_309145,RMVar_hsa_circ_277175,RMVar_hsa_circ_213618 89953 RMVar_ID_89953 Human_SNP_ID_701344192 m1A Human chr22 - 29288697 29288697 29288697 CCCCCTCTTCCCCTGCCCCGGTTATCAGGGCCACTCATGCTCCGGTTCTCTCCTGGTCCGGAAAA CCCCCTCTTCCCCTGCCCCGGTTATCAGGGCCTCTCATGCTCCGGTTCTCTCCTGGTCCGGAAAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29288651..29288808;chr22:29288651..29288846 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89954 RMVar_ID_89954 Human_SNP_ID_701344193 m1A Human chr22 - 29288697 29288697 29288697 CCCCCTCTTCCCCTGCCCCGGTTATCAGGGCCACTCATGCTCCGGTTCTCTCCTGGTCCGGAAAA CCCCCTCTTCCCCTGCCCCGGTTATCAGGGCCGCTCATGCTCCGGTTCTCTCCTGGTCCGGAAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29288651..29288808;chr22:29288651..29288846 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89955 RMVar_ID_89955 Human_SNP_ID_701346752 m1A Human chr22 + 29297875 29297875 29297875 GAGCAAACTTAAAGTCTCCCTTGCTCGGAAGAAGCCTCCAATGAACAGTATGCGGGGTGGTCTGC GAGCAAACTTAAAGTCTCCCTTGCTCGGAAGACGCCTCCAATGAACAGTATGCGGGGTGGTCTGC A C EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:29296251..29297876 32194978 MeRIP-seq:(Medium) rs780205458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1609723,Human_RBP_ID_1941362,Human_RBP_ID_3670764,Human_RBP_ID_3962291,Human_RBP_ID_7072707,Human_RBP_ID_8862375,Human_RBP_ID_9125543,Human_RBP_ID_9260679,Human_RBP_ID_9392108,Human_RBP_ID_14445032,Human_RBP_ID_18786769,Human_RBP_ID_19007832,Human_RBP_ID_22454402,Human_RBP_ID_23941997 Human_Splice_Rec_2150464,Human_Splice_Rec_2150465,Human_Splice_Rec_2150492,Human_Splice_Rec_2150493,Human_Splice_Rec_2150524,Human_Splice_Rec_2150525,Human_Splice_Rec_2150588,Human_Splice_Rec_2150589,Human_Splice_Rec_2150640,Human_Splice_Rec_2150641,Human_Splice_Rec_2150688,Human_Splice_Rec_2150689,Human_Splice_Rec_2150746,Human_Splice_Rec_2150747,Human_Splice_Rec_2150774,Human_Splice_Rec_2150775,Human_Splice_Rec_2150788,Human_Splice_Rec_2150789,Human_Splice_Rec_2150802,Human_Splice_Rec_2150803,Human_Splice_Rec_2150814,Human_Splice_Rec_2150815,Human_Splice_Rec_2150824,Human_Splice_Rec_2150825 RMVar_hsa_circ_38608,RMVar_hsa_circ_53612 89956 RMVar_ID_89956 Human_SNP_ID_701347112 m1A Human chr22 + 29298818 29298818 29298818 GGAGGAGATAGAGGAGGCTTCCCTCCAAGAGGACCCCGGGGTTCCCGAGGGAACCCCTCTGGAGG GGAGGAGATAGAGGAGGCTTCCCTCCAAGAGGGCCCCGGGGTTCCCGAGGGAACCCCTCTGGAGG A G EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29298775..29298902 26863196 MeRIP-seq:(Medium) rs753034592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66045,Human_RBP_ID_577658,Human_RBP_ID_930741,Human_RBP_ID_1307373,Human_RBP_ID_1941364,Human_RBP_ID_4691186,Human_RBP_ID_9392112,Human_RBP_ID_18471463,Human_RBP_ID_19007834,Human_RBP_ID_22454404,Human_RBP_ID_23015411,Human_RBP_ID_26344894 Human_Splice_Rec_2150466,Human_Splice_Rec_2150467,Human_Splice_Rec_2150494,Human_Splice_Rec_2150495,Human_Splice_Rec_2150526,Human_Splice_Rec_2150527,Human_Splice_Rec_2150590,Human_Splice_Rec_2150591,Human_Splice_Rec_2150642,Human_Splice_Rec_2150643,Human_Splice_Rec_2150690,Human_Splice_Rec_2150691,Human_Splice_Rec_2150748,Human_Splice_Rec_2150749,Human_Splice_Rec_2150776,Human_Splice_Rec_2150777,Human_Splice_Rec_2150790,Human_Splice_Rec_2150791,Human_Splice_Rec_2150804,Human_Splice_Rec_2150816,Human_Splice_Rec_2150817,Human_Splice_Rec_2150826 RMVar_hsa_circ_65970 89957 RMVar_ID_89957 Human_SNP_ID_701347132 m1A Human chr22 + 29298851 29298851 29298851 CCCCGGGGTTCCCGAGGGAACCCCTCTGGAGGAGGAAACGTCCAGCACCGAGCTGGAGACTGGCA CCCCGGGGTTCCCGAGGGAACCCCTCTGGAGGTGGAAACGTCCAGCACCGAGCTGGAGACTGGCA A T EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs375087308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246710,Human_RBP_ID_577658,Human_RBP_ID_930741,Human_RBP_ID_4691186,Human_RBP_ID_9125544,Human_RBP_ID_9392112,Human_RBP_ID_18471463,Human_RBP_ID_19007834,Human_RBP_ID_22454404,Human_RBP_ID_23015411,Human_RBP_ID_26344895 Human_Splice_Rec_2150467,Human_Splice_Rec_2150495,Human_Splice_Rec_2150527,Human_Splice_Rec_2150591,Human_Splice_Rec_2150643,Human_Splice_Rec_2150691,Human_Splice_Rec_2150749,Human_Splice_Rec_2150777,Human_Splice_Rec_2150791,Human_Splice_Rec_2150817 RMVar_hsa_circ_65970 89958 RMVar_ID_89958 Human_SNP_ID_701347275 m1A Human chr22 - 29299297 29299297 29299297 GGGGGCGGAAAGGGTGGCGGGAGGAAGCCTTCAGGCTTTGGGGCCTTACACTGGTTGCACTCTGT GGGGGCGGAAAGGGTGGCGGGAGGAAGCCTTCGGGCTTTGGGGCCTTACACTGGTTGCACTCTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29299246..29299367 26863196 MeRIP-seq:(Medium) rs1318330179 Functional Loss SNV dbSNP153 33..33 33 - - - 89959 RMVar_ID_89959 Human_SNP_ID_701347283 m1A Human chr22 - 29299321 29299321 29299321 CACTCATGAAACCTGCACCTACCCGGGGGCGGAAAGGGTGGCGGGAGGAAGCCTTCAGGCTTTGG CACTCATGAAACCTGCACCTACCCGGGGGCGGGAAGGGTGGCGGGAGGAAGCCTTCAGGCTTTGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29299226..29299350 32194978 MeRIP-seq:(Medium) rs369377914 Functional Loss SNV dbSNP153 33..33 33 - - - 89960 RMVar_ID_89960 Human_SNP_ID_701347430 m1A Human chr22 + 29299704 29299683 29299704 CGGTGGAATGTTCAGAGGTGGCCGTGGTGGAGACAGAGGTGGCTTCCGTGGTGGCCGGGGCATGG CGGTGGAATGTT_____________________CAGAGGTGGCTTCCGTGGTGGCCGGGGCATGG TCAGAGGTGGCCGTGGTGGAGA T EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs756091192 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_7072715,Human_RBP_ID_9260680,Human_RBP_ID_9300325,Human_RBP_ID_9354254,Human_RBP_ID_17984245,Human_RBP_ID_22454883,Human_RBP_ID_23942017,Human_RBP_ID_25663564,Human_RBP_ID_26345853,Human_RBP_ID_27306276 89961 RMVar_ID_89961 Human_SNP_ID_701347441 m1A Human chr22 - 29299711 29299711 29299711 CCTCGGTCCATGCCCCGGCCACCACGGAAGCCACCTCTGTCTCCACCACGGCCACCTCTGAACAT CCTCGGTCCATGCCCCGGCCACCACGGAAGCCCCCTCTGTCTCCACCACGGCCACCTCTGAACAT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:29299576..29299875 26863196 MeRIP-seq:(Medium) rs766181979 Functional Loss SNV dbSNP153 33..33 33 - - - 89962 RMVar_ID_89962 Human_SNP_ID_701347454 m1A Human chr22 - 29299744 29299744 29299744 CCAGGGCCACCTCGTCTTCCTCCACCAAAGCCACCTCGGTCCATGCCCCGGCCACCACGGAAGCC CCAGGGCCACCTCGTCTTCCTCCACCAAAGCCCCCTCGGTCCATGCCCCGGCCACCACGGAAGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29299601..29299875 26863196 MeRIP-seq:(Medium) rs769896639 Functional Loss SNV dbSNP153 33..33 33 - - - 89963 RMVar_ID_89963 Human_SNP_ID_701347475 m1A Human chr22 - 29299786 29299786 29299786 CTTCTTCCTCCCATCTGTTCCATCAAAGGTCCAGGGGGCCCCCCAGGGCCACCTCGTCTTCCTCC CTTCTTCCTCCCATCTGTTCCATCAAAGGTCCGGGGGGCCCCCCAGGGCCACCTCGTCTTCCTCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:29299651..29299875 26863196 MeRIP-seq:(Medium) rs1249972689 Functional Loss SNV dbSNP153 33..33 33 - - - 89964 RMVar_ID_89964 Human_SNP_ID_701349863 m1A Human chr22 - 29307118 29307118 29307118 GCTCATCCCGCGGCCCCGGGGAGCATTGCCCCAGCGGGGGCCGGAGCCGGGCCGGGCCGCCGCAG GCTCATCCCGCGGCCCCGGGGAGCATTGCCCCGGCGGGGGCCGGAGCCGGGCCGGGCCGCCGCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29307069..29307193 26863196 MeRIP-seq:(Medium) rs1463575648 Functional Loss SNV dbSNP153 33..33 33 - - - 89965 RMVar_ID_89965 Human_SNP_ID_701350380 m1A Human chr22 + 29308624 29308624 29308624 GAGATTGAGCGGGAGCTGCGTGCTGCACCCCCAGCCCCCAACGCCCCTGCCGCTGGGGAGGACAC GAGATTGAGCGGGAGCTGCGTGCTGCACCCCCTGCCCCCAACGCCCCTGCCGCTGGGGAGGACAC A T GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29308577..29308700 26863196 MeRIP-seq:(Medium) rs1274591072 Functional Loss SNV dbSNP153 33..33 33 - - - 89966 RMVar_ID_89966 Human_SNP_ID_701351223 m1A Human chr22 + 29310923 29310923 29310923 TCCCCGCCCTGCTAGCCCAGTCCCTGGGAGTGAGCGCCGGGGCTCCCGGCCTGAGATGACTCCCG TCCCCGCCCTGCTAGCCCAGTCCCTGGGAGTGTGCGCCGGGGCTCCCGGCCTGAGATGACTCCCG A T GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29310876..29311043 26863196 MeRIP-seq:(Medium) rs746842839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2150836,Human_Splice_Rec_2150837,Human_Splice_Rec_2150852,Human_Splice_Rec_2150853,Human_Splice_Rec_2150862,Human_Splice_Rec_2150870,Human_Splice_Rec_2150871,Human_Splice_Rec_2150880,Human_Splice_Rec_2150881,Human_Splice_Rec_2150890,Human_Splice_Rec_2150891,Human_Splice_Rec_2150896 RMVar_hsa_circ_378098 89967 RMVar_ID_89967 Human_SNP_ID_701351783 m1A Human chr22 - 29312046 29312045 29312046 GTCCAGTGGGGGTCACGCTAGCAACAGCCTCAAGGGCCCGGGCATTGGCCAGGAACTCCTCTTCC GTCCAGTGGGGGTCACGCTAGCAACAGCCTCA_GGGCCCGGGCATTGGCCAGGAACTCCTCTTCC CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29311995..29312518 26863196 MeRIP-seq:(Medium) rs1456349837 Functional Loss DEL dbSNP153 33..33 33 - - - 89968 RMVar_ID_89968 Human_SNP_ID_701351815 m1A Human chr22 + 29312106 29312105 29312106 TGGACCAGCCCCTGACCCAGCTCGGGCCCCCGACCCTCCAGCTCCTGACTCTGCCTATTGTTCCT TGGACCAGCCCCTGACCCAGCTCGGGCCCCCG_CCCTCCAGCTCCTGACTCTGCCTATTGTTCCT GA G GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29311684..29312602 26863196 MeRIP-seq:(Medium) rs774571768 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_577685,Human_RBP_ID_8548067,Human_RBP_ID_27492792 Human_miRNA_ID_2293178,Human_miRNA_ID_2358528,Human_miRNA_ID_3060965 89969 RMVar_ID_89969 Human_SNP_ID_701351859 m1A Human chr22 + 29312234 29312234 29312234 GCCGGACGGCCAATGGGCTGCCTGGGCCCCGAAGCCAAGCCCTTTCCAGCTCCTCCGATGAAGGC GCCGGACGGCCAATGGGCTGCCTGGGCCCCGACGCCAAGCCCTTTCCAGCTCCTCCGATGAAGGC A C GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29311490..29312540 26863196 MeRIP-seq:(Medium) rs750076971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152401,Human_RBP_ID_27492792,Human_RBP_ID_27565250 Human_Splice_Rec_2150854 Human_miRNA_ID_3060966 89970 RMVar_ID_89970 Human_SNP_ID_701351860 m1A Human chr22 + 29312234 29312234 29312234 GCCGGACGGCCAATGGGCTGCCTGGGCCCCGAAGCCAAGCCCTTTCCAGCTCCTCCGATGAAGGC GCCGGACGGCCAATGGGCTGCCTGGGCCCCGAGGCCAAGCCCTTTCCAGCTCCTCCGATGAAGGC A G GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29311490..29312540 26863196 MeRIP-seq:(Medium) rs750076971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152401,Human_RBP_ID_27492792,Human_RBP_ID_27565250 Human_Splice_Rec_2150854 Human_miRNA_ID_3060966 89971 RMVar_ID_89971 Human_SNP_ID_701356161 m1A Human chr22 + 29328047 29328047 29328047 GCCCCATCTCTCGGCCCAGTCTTTGTGGCAGGAGGCCTGGGCTCAGAGGCGACACTGAGGAATGT GCCCCATCTCTCGGCCCAGTCTTTGTGGCAGGGGGCCTGGGCTCAGAGGCGACACTGAGGAATGT A G L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29328000..29328191 26863196 MeRIP-seq:(Medium) rs1360597024 Functional Loss SNV dbSNP153 33..33 33 - - - 89972 RMVar_ID_89972 Human_SNP_ID_701356851 m1A Human chr22 - 29330372 29330372 29330372 ATCCAGCCGGGCAACCCCAGCTGCACGGTGAGAGCCCCGGCACCCGCCCTGCAGCCTTGGAGCCT ATCCAGCCGGGCAACCCCAGCTGCACGGTGAGGGCCCCGGCACCCGCCCTGCAGCCTTGGAGCCT T C AP1B1 Ensembl:ENSG00000100280 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29330367..29330657 32194978 MeRIP-seq:(Medium) rs1460728272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19111810 RMVar_hsa_circ_213620,RMVar_hsa_circ_90876 89973 RMVar_ID_89973 Human_SNP_ID_701357942 m1A Human chr22 - 29334341 29334341 29334341 TCTCAGGCACCTTCACCCGCCAGGTGGGCTCCATCTCCATGGACCTGCAGCTGACCAACAAGGCC TCTCAGGCACCTTCACCCGCCAGGTGGGCTCCGTCTCCATGGACCTGCAGCTGACCAACAAGGCC T C AP1B1 Ensembl:ENSG00000100280 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29334290..29341611 32194978 MeRIP-seq:(Medium) rs1206377658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_577731,Human_RBP_ID_9300653,Human_RBP_ID_18194068,Human_RBP_ID_22454409,Human_RBP_ID_26822355 Human_Splice_Rec_2150944,Human_Splice_Rec_2150945,Human_Splice_Rec_2150986,Human_Splice_Rec_2150987,Human_Splice_Rec_2151028,Human_Splice_Rec_2151029,Human_Splice_Rec_2151070,Human_Splice_Rec_2151071,Human_Splice_Rec_2151108,Human_Splice_Rec_2151109,Human_Splice_Rec_2151146,Human_Splice_Rec_2151147,Human_Splice_Rec_2151160,Human_Splice_Rec_2151161 Human_miRNA_ID_1985605,Human_miRNA_ID_2941254 RMVar_hsa_circ_213620,RMVar_hsa_circ_90876,RMVar_hsa_circ_120891,RMVar_hsa_circ_110133,RMVar_hsa_circ_213621,RMVar_hsa_circ_213622,RMVar_hsa_circ_24725 89974 RMVar_ID_89974 Human_SNP_ID_701369580 m1A Human chr22 - 29380955 29380955 29380955 GGGTAATGGCCAGCAGGGTGCATGCGTGAGAGAGGAGGGGCATGCATCTCTTATAGGACCTGTGG GGGTAATGGCCAGCAGGGTGCATGCGTGAGAGGGGAGGGGCATGCATCTCTTATAGGACCTGTGG T C AP1B1 Ensembl:ENSG00000100280 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29380952..29381129 26863196 MeRIP-seq:(Medium) rs143633819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18786834 RMVar_hsa_circ_317152,RMVar_hsa_circ_83859,RMVar_hsa_circ_213638 89975 RMVar_ID_89975 Human_SNP_ID_701411470 m1A Human chr22 - 29543544 29543544 29543544 CGTCAGTGGGCTTTACTGTTTTCTTTGCCCACAGGCAATAGAAATAGAAGAACGGAGGATCCAGA CGTCAGTGGGCTTTACTGTTTTCTTTGCCCACTGGCAATAGAAATAGAAGAACGGAGGATCCAGA T A THOC5 Ensembl:ENSG00000100296 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29543510..29545086 26863196 MeRIP-seq:(Medium) rs112210447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14446810,Human_RBP_ID_27821591 RMVar_hsa_circ_360960,RMVar_hsa_circ_48679,RMVar_hsa_circ_23285,RMVar_hsa_circ_303976,RMVar_hsa_circ_55912,RMVar_hsa_circ_30143,RMVar_hsa_circ_60989 89976 RMVar_ID_89976 Human_SNP_ID_701411745 m1A Human chr22 - 29544595 29544595 29544595 GAGCCTTTATCCTTACCTCTACAGGAAGGTAAATACTACAGTGAGGAGGCCGAGGTGGATCTGCG GAGCCTTTATCCTTACCTCTACAGGAAGGTAACTACTACAGTGAGGAGGCCGAGGTGGATCTGCG T G THOC5 Ensembl:ENSG00000100296 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29544451..29544625 26863196 MeRIP-seq:(Medium) rs753777475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929369,Human_RBP_ID_9392140,Human_RBP_ID_18786870,Human_RBP_ID_19007850,Human_RBP_ID_26345280 Human_Splice_Rec_2151262,Human_Splice_Rec_2151302,Human_Splice_Rec_2151340,Human_Splice_Rec_2151380,Human_Splice_Rec_2151422,Human_Splice_Rec_2151462,Human_Splice_Rec_2151538,Human_Splice_Rec_2151552,Human_Splice_Rec_2151562,Human_Splice_Rec_2151572,Human_Splice_Rec_2151584,Human_Splice_Rec_2151594 RMVar_hsa_circ_360960,RMVar_hsa_circ_48679,RMVar_hsa_circ_23285,RMVar_hsa_circ_303976,RMVar_hsa_circ_55912,RMVar_hsa_circ_30143,RMVar_hsa_circ_60989 89977 RMVar_ID_89977 Human_SNP_ID_701414662 m1A Human chr22 - 29555314 29555309 29555315 GATGGGAGCCAGGAAAGATTTAGGGGCAGGAGACAGACACGTAACAGGAACTCGGAAGGTAGAAC GATGGGAGCCAGGAAAGATTTAGGGGCAGGA______CACGTAACAGGAACTCGGAAGGTAGAAC GTCTGTC G NIPSNAP1 Ensembl:ENSG00000184117 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29555201..29555418 26863196 MeRIP-seq:(Medium) rs1270066924 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_577802,Human_RBP_ID_7073182,Human_RBP_ID_14446922,Human_RBP_ID_26500110 RMVar_hsa_circ_213652,RMVar_hsa_circ_80436,RMVar_hsa_circ_122749,RMVar_hsa_circ_213653 89978 RMVar_ID_89978 Human_SNP_ID_701414670 m1A Human chr22 - 29555333 29555333 29555333 CAGAGGGGCTGGGGAAAGGGATGGGAGCCAGGAAAGATTTAGGGGCAGGAGACAGACACGTAACA CAGAGGGGCTGGGGAAAGGGATGGGAGCCAGGGAAGATTTAGGGGCAGGAGACAGACACGTAACA T C NIPSNAP1 Ensembl:ENSG00000184117 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29555185..29555449 26863196 MeRIP-seq:(Medium) rs565768950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_577802,Human_RBP_ID_7073183,Human_RBP_ID_8208605,Human_RBP_ID_17069208,Human_RBP_ID_17399778,Human_RBP_ID_23942165,Human_RBP_ID_26500110 RMVar_hsa_circ_213652,RMVar_hsa_circ_80436,RMVar_hsa_circ_122749,RMVar_hsa_circ_213653 89979 RMVar_ID_89979 Human_SNP_ID_701414740 m1A Human chr22 - 29555709 29555709 29555709 TCCCTGCCTGCCTCCCTCCCCCTGCTAGAAGTAGTTTCTGATTTCCCTGAATGAAAGATAGTGAT TCCCTGCCTGCCTCCCTCCCCCTGCTAGAAGTCGTTTCTGATTTCCCTGAATGAAAGATAGTGAT T G NIPSNAP1 Ensembl:ENSG00000184117 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29555659..29555828 26863196 MeRIP-seq:(Medium) rs545726376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_577814,Human_RBP_ID_781670,Human_RBP_ID_3670859,Human_RBP_ID_4691561,Human_RBP_ID_18952908,Human_RBP_ID_22820095,Human_RBP_ID_23942170,Human_RBP_ID_26500116 Human_miRNA_ID_2213317,Human_miRNA_ID_2766225 RMVar_hsa_circ_213652,RMVar_hsa_circ_80436,RMVar_hsa_circ_122749,RMVar_hsa_circ_213653 89980 RMVar_ID_89980 Human_SNP_ID_701418329 m1A Human chr22 - 29570473 29570473 29570473 CTGGTTCCGCTCCCTCTTTGTTCACAAAGTGGATCCCCGGAAGGATGCCCACTCCACCCTGCTGT CTGGTTCCGCTCCCTCTTTGTTCACAAAGTGGTTCCCCGGAAGGATGCCCACTCCACCCTGCTGT T A NIPSNAP1 Ensembl:ENSG00000184117 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29570401..29570570 26863196 MeRIP-seq:(Medium) rs796797747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708546,Human_RBP_ID_22454889,Human_RBP_ID_27035018 Human_Splice_Rec_2151600,Human_Splice_Rec_2151601,Human_Splice_Rec_2151618,Human_Splice_Rec_2151619,Human_Splice_Rec_2151634,Human_Splice_Rec_2151635,Human_Splice_Rec_2151646,Human_Splice_Rec_2151647,Human_Splice_Rec_2151658,Human_Splice_Rec_2151659 RMVar_hsa_circ_66410,RMVar_hsa_circ_338107,RMVar_hsa_circ_346710,RMVar_hsa_circ_69306,RMVar_hsa_circ_213658 89981 RMVar_ID_89981 Human_SNP_ID_701418351 m1A Human chr22 + 29570532 29570532 29570532 AACCAGCTGCCTTCATTGTCCTTGGAATAGAAACTGCAGGACAGAGGAGTTGAGGGGGACGCGCG AACCAGCTGCCTTCATTGTCCTTGGAATAGAAGCTGCAGGACAGAGGAGTTGAGGGGGACGCGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29570364..29570581 26863196 MeRIP-seq:(Medium) rs774231400 Functional Loss SNV dbSNP153 33..33 33 - - - 89982 RMVar_ID_89982 Human_SNP_ID_701420956 m1A Human chr22 - 29580806 29580806 29580806 TCTGGGCAAAGAATGGGGGAGGTGAGAAAGGGATGGGTAGGGTCTTTGTCCTGGTTGGGACCGGG TCTGGGCAAAGAATGGGGGAGGTGAGAAAGGGCTGGGTAGGGTCTTTGTCCTGGTTGGGACCGGG T G NIPSNAP1 Ensembl:ENSG00000184117 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:29580773..29580902 26863196 MeRIP-seq:(Medium) rs963674816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5324164,Human_RBP_ID_8207288,Human_RBP_ID_8235503,Human_RBP_ID_9432850,Human_RBP_ID_17659994,Human_RBP_ID_18952494,Human_RBP_ID_22725435,Human_RBP_ID_23942187 89983 RMVar_ID_89983 Human_SNP_ID_701421023 m1A Human chr22 + 29581036 29581036 29581036 CAACGTCCCCAGCGCGAGGCCCCGGGCCCCCCAGCAGCCGCCGCGCCGTCACAGAGATGCTGCAC CAACGTCCCCAGCGCGAGGCCCCGGGCCCCCCCGCAGCCGCCGCGCCGTCACAGAGATGCTGCAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29580976..29581075 32194978 MeRIP-seq:(Medium) rs903389615 Functional Loss SNV dbSNP153 33..33 33 - - - 89984 RMVar_ID_89984 Human_SNP_ID_701421048 m1A Human chr22 + 29581067 29581067 29581067 CAGCAGCCGCCGCGCCGTCACAGAGATGCTGCACAGCCGCGGAGCCATGTTGGAGCCGCAAAGGT CAGCAGCCGCCGCGCCGTCACAGAGATGCTGCGCAGCCGCGGAGCCATGTTGGAGCCGCAAAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29580632..29581125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89985 RMVar_ID_89985 Human_SNP_ID_701421049 m1A Human chr22 + 29581067 29581067 29581067 CAGCAGCCGCCGCGCCGTCACAGAGATGCTGCACAGCCGCGGAGCCATGTTGGAGCCGCAAAGGT CAGCAGCCGCCGCGCCGTCACAGAGATGCTGCTCAGCCGCGGAGCCATGTTGGAGCCGCAAAGGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29580632..29581125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 89986 RMVar_ID_89986 Human_SNP_ID_701443382 m1A Human chr22 + 29671901 29671901 29671901 AGGCTGAACGCACGAGGGATGAGTTGGAGAGGAGGCTGCTGCAGATGAAAGAAGAAGCAACAATG AGGCTGAACGCACGAGGGATGAGTTGGAGAGGGGGCTGCTGCAGATGAAAGAAGAAGCAACAATG A G NF2 Ensembl:ENSG00000186575 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29671797..29674950;chr22:29671790..29673521;chr22:29671776..29673538 26863196 MeRIP-seq:(Medium) rs1465752977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66111,Human_RBP_ID_782433,Human_RBP_ID_1941447,Human_RBP_ID_5389054,Human_RBP_ID_7073339,Human_RBP_ID_9392150,Human_RBP_ID_14448294,Human_RBP_ID_17989388,Human_RBP_ID_26345287 Human_Splice_Rec_2151692,Human_Splice_Rec_2151693,Human_Splice_Rec_2151723,Human_Splice_Rec_2151754,Human_Splice_Rec_2151755,Human_Splice_Rec_2151786,Human_Splice_Rec_2151787,Human_Splice_Rec_2151818,Human_Splice_Rec_2151819,Human_Splice_Rec_2151848,Human_Splice_Rec_2151849,Human_Splice_Rec_2151878,Human_Splice_Rec_2151879,Human_Splice_Rec_2151906,Human_Splice_Rec_2151907,Human_Splice_Rec_2151934,Human_Splice_Rec_2151935,Human_Splice_Rec_2151978,Human_Splice_Rec_2151979,Human_Splice_Rec_2152010,Human_Splice_Rec_2152011,Human_Splice_Rec_2152044,Human_Splice_Rec_2152045,Human_Splice_Rec_2152064,Human_Splice_Rec_2152065 RMVar_hsa_circ_28274,RMVar_hsa_circ_39428,RMVar_hsa_circ_213661,RMVar_hsa_circ_73862,RMVar_hsa_circ_71457,RMVar_hsa_circ_7241 89987 RMVar_ID_89987 Human_SNP_ID_701444164 m1A Human chr22 - 29674769 29674769 29674769 AGAGGGCAGGTAGCAGGAAAAGACACCACCCCACCCCTGCAGAGGAGGGACCTGGGCTAACCCTG AGAGGGCAGGTAGCAGGAAAAGACACCACCCCCCCCCTGCAGAGGAGGGACCTGGGCTAACCCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29674767..29674854 26863196 MeRIP-seq:(Medium) rs553181672 Functional Loss SNV dbSNP153 33..33 33 - - - 89988 RMVar_ID_89988 Human_SNP_ID_701449374 m1A Human chr22 + 29697214 29697214 29697214 TTTGTTCTTTAACAATGGCTGCAGGTGGGAGCATATGGTGGTTTATAAAAACGCTGTCGGGCTTT TTTGTTCTTTAACAATGGCTGCAGGTGGGAGCGTATGGTGGTTTATAAAAACGCTGTCGGGCTTT A G NF2 Ensembl:ENSG00000186575 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1311012306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14448905,Human_RBP_ID_17984368,Human_RBP_ID_18328459 RMVar_hsa_circ_213667 89989 RMVar_ID_89989 Human_SNP_ID_701458248 m1A Human chr22 - 29731356 29731356 29731356 CTCTTATTCTCCCCGCTTCTCTCTCTCTCTCTAGGGCTGAACCCATCAGAACCACTGTCTTCCAG CTCTTATTCTCCCCGCTTCTCTCTCTCTCTCTGGGGCTGAACCCATCAGAACCACTGTCTTCCAG T C ZMAT5 Ensembl:ENSG00000100319 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:29731305..29738431 32194978 MeRIP-seq:(Medium) rs1569332706 Functional Loss SNV dbSNP153 33..33 33 - - - 89990 RMVar_ID_89990 Human_SNP_ID_701459977 m1A Human chr22 + 29737956 29737956 29737956 TTTTCCCGTCTGTGTGCCCTCGGGCAAGTCGCACCCTCCCTGTTTTCCCTTCTGCAAGGCCCTAG TTTTCCCGTCTGTGTGCCCTCGGGCAAGTCGCCCCCTCCCTGTTTTCCCTTCTGCAAGGCCCTAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29737927..29738099 26863196 MeRIP-seq:(Medium) rs866573822 Functional Loss SNV dbSNP153 33..33 33 - - - 89991 RMVar_ID_89991 Human_SNP_ID_701462560 m1A Human chr22 - 29748566 29748566 29748566 TAATCTGAGCTCTTTGTGGCTTCCCAGGCAGCAAAGCACCTGCTCTGAGTGGCCATGGGGAAGCG TAATCTGAGCTCTTTGTGGCTTCCCAGGCAGCCAAGCACCTGCTCTGAGTGGCCATGGGGAAGCG T G ZMAT5 Ensembl:ENSG00000100319 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29748560..29767011 26863196 MeRIP-seq:(Medium) rs761151544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4711163 Human_Splice_Rec_2152092,Human_Splice_Rec_2152102 Human_miRNA_ID_2253636 RMVar_hsa_circ_1894,RMVar_hsa_circ_54539,RMVar_hsa_circ_213670,RMVar_hsa_circ_371035,RMVar_hsa_circ_333910,RMVar_hsa_circ_213671 89992 RMVar_ID_89992 Human_SNP_ID_701467222 m1A Human chr22 - 29767426 29767426 29767426 GGTGGAGGTCCTGCGGAACAGCAGGGAGTACAATTTCGAAGTCAACGTCGCGGCCGCCATGTTTC GGTGGAGGTCCTGCGGAACAGCAGGGAGTACAGTTTCGAAGTCAACGTCGCGGCCGCCATGTTTC T C AC004882.4 Ensembl:ENSG00000287967 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29767376..29767425 26863196 MeRIP-seq:(Medium) rs770281965 Functional Loss SNV dbSNP153 33..33 33 - - - 89993 RMVar_ID_89993 Human_SNP_ID_701467223 m1A Human chr22 - 29767427 29767427 29767427 AGGTGGAGGTCCTGCGGAACAGCAGGGAGTACAATTTCGAAGTCAACGTCGCGGCCGCCATGTTT AGGTGGAGGTCCTGCGGAACAGCAGGGAGTACCATTTCGAAGTCAACGTCGCGGCCGCCATGTTT T G AC004882.4 Ensembl:ENSG00000287967 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:29767376..29767586;chr22:29767376..29767525;chr22:29767376..29767555;chr22:29767376..29767450 26863196 MeRIP-seq:(Medium) rs372163897 Functional Loss SNV dbSNP153 33..33 33 - - - 89994 RMVar_ID_89994 Human_SNP_ID_701467239 m1A Human chr22 + 29767447 29767447 29767447 TGACTTCGAAATTGTACTCCCTGCTGTTCCGCAGGACCTCCACCTTCGCCCTCACCATCATCGTG TGACTTCGAAATTGTACTCCCTGCTGTTCCGCGGGACCTCCACCTTCGCCCTCACCATCATCGTG A G UQCR10 Ensembl:ENSG00000184076 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:29767401..29767475 26863196 MeRIP-seq:(Medium) rs567943107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_577895,Human_RBP_ID_931663,Human_RBP_ID_1307409,Human_RBP_ID_1609837,Human_RBP_ID_3670921,Human_RBP_ID_4691865,Human_RBP_ID_5446374,Human_RBP_ID_5504528,Human_RBP_ID_8548210,Human_RBP_ID_8862492,Human_RBP_ID_17285463,Human_RBP_ID_17514662,Human_RBP_ID_17660242,Human_RBP_ID_22268387,Human_RBP_ID_22454414,Human_RBP_ID_22820114,Human_RBP_ID_23212728,Human_RBP_ID_27035079,Human_RBP_ID_27306425 RMVar_hsa_circ_94407,RMVar_hsa_circ_213673 89995 RMVar_ID_89995 Human_SNP_ID_701467280 m1A Human chr22 + 29767508 29767508 29767508 CGTGGGCGTCATGTTCTTCGAGCGCGCCTTCGATCAAGGCGCGGACGCTATCTACGACCACATCA CGTGGGCGTCATGTTCTTCGAGCGCGCCTTCGGTCAAGGCGCGGACGCTATCTACGACCACATCA A G AC004882.4 Ensembl:ENSG00000287967 lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV HGVD 33..33 33 - - - 89996 RMVar_ID_89996 Human_SNP_ID_701473287 m1A Human chr22 - 29792490 29792490 29792490 CCTCAGGTGCTGAGAACCAAAGTGCCTAGAGAAGGGCAGGAGGAGGATGACGACGATGAGGAAGA CCTCAGGTGCTGAGAACCAAAGTGCCTAGAGAGGGGCAGGAGGAGGATGACGACGATGAGGAAGA T C ASCC2 Ensembl:ENSG00000100325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29792398..29792526 26863196 MeRIP-seq:(Medium) rs1178276469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7073566 Human_Splice_Rec_2152142,Human_Splice_Rec_2152143,Human_Splice_Rec_2152154,Human_Splice_Rec_2152155,Human_Splice_Rec_2152192,Human_Splice_Rec_2152193,Human_Splice_Rec_2152238,Human_Splice_Rec_2152239,Human_Splice_Rec_2152278,Human_Splice_Rec_2152279 Human_miRNA_ID_3119296 RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213678,RMVar_hsa_circ_101814,RMVar_hsa_circ_213677 89997 RMVar_ID_89997 Human_SNP_ID_701473636 m1A Human chr22 + 29793644 29793644 29793644 GCCGCTGTGCCGCCACTGCACGCTTGTCGTTCAGCAAACTCCGCGTGTTTTCCTCCTTCCTGGTG GCCGCTGTGCCGCCACTGCACGCTTGTCGTTCGGCAAACTCCGCGTGTTTTCCTCCTTCCTGGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29793593..29799211 32194978 MeRIP-seq:(Medium) rs982424605 Functional Loss SNV dbSNP153 33..33 33 - - - 89998 RMVar_ID_89998 Human_SNP_ID_701475568 m1A Human chr22 - 29802072 29802072 29802072 CATCCTGGCCTGCCTGGAGTACTACCACTACGACCCAGAGCAGGTGATCAACAATATCCTGGAGG CATCCTGGCCTGCCTGGAGTACTACCACTACGTCCCAGAGCAGGTGATCAACAATATCCTGGAGG T A ASCC2 Ensembl:ENSG00000100325 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29800997..29804658 32194978 MeRIP-seq:(Medium) rs752966932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529888 Human_Splice_Rec_2152135,Human_Splice_Rec_2152149,Human_Splice_Rec_2152185,Human_Splice_Rec_2152271,Human_Splice_Rec_2152283 Human_miRNA_ID_2425895,Human_miRNA_ID_2435565,Human_miRNA_ID_2908872,Human_miRNA_ID_3027715 RMVar_hsa_circ_16666,RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_95696,RMVar_hsa_circ_213678,RMVar_hsa_circ_101814,RMVar_hsa_circ_213677,RMVar_hsa_circ_114350,RMVar_hsa_circ_213680,RMVar_hsa_circ_379050,RMVar_hsa_circ_213681,RMVar_hsa_circ_17298,RMVar_hsa_circ_1091 89999 RMVar_ID_89999 Human_SNP_ID_701479648 m1A Human chr22 - 29818732 29818732 29818732 GGCTGCAGGTATCCAGAGGGGACTGCGTGGTGATGGGAGAGTGAGAAAGCCTACTCACTTACTGC GGCTGCAGGTATCCAGAGGGGACTGCGTGGTGGTGGGAGAGTGAGAAAGCCTACTCACTTACTGC T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29818729..29818982 26863196 MeRIP-seq:(Medium) rs1305992504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5204622,Human_RBP_ID_7073597 RMVar_hsa_circ_293,RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213677,RMVar_hsa_circ_17298,RMVar_hsa_circ_109203,RMVar_hsa_circ_1091,RMVar_hsa_circ_213682,RMVar_hsa_circ_28387,RMVar_hsa_circ_299386,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_377201,RMVar_hsa_circ_289091,RMVar_hsa_circ_98815,RMVar_hsa_circ_111127,RMVar_hsa_circ_49828,RMVar_hsa_circ_213685,RMVar_hsa_circ_213687,RMVar_hsa_circ_213689,RMVar_hsa_circ_213688,RMVar_hsa_circ_213686,RMVar_hsa_circ_75235,RMVar_hsa_circ_213691,RMVar_hsa_circ_123113,RMVar_hsa_circ_311739,RMVar_hsa_circ_213692 90000 RMVar_ID_90000 Human_SNP_ID_701482033 m1A Human chr22 - 29827710 29827710 29827710 CCTGGCCTGAGTGAGAAGTGAGGGAAGAGGTAAAGTGCCAACAGATAGAAGAGGGAGGAAGCTTG CCTGGCCTGAGTGAGAAGTGAGGGAAGAGGTATAGTGCCAACAGATAGAAGAGGGAGGAAGCTTG T A ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29827703..29827985 26863196 MeRIP-seq:(Medium) rs1234695404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5298259,Human_RBP_ID_5653451,Human_RBP_ID_17286718,Human_RBP_ID_23942364 RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213677,RMVar_hsa_circ_1091,RMVar_hsa_circ_41965,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_98815,RMVar_hsa_circ_213685,RMVar_hsa_circ_213686,RMVar_hsa_circ_213691,RMVar_hsa_circ_123113,RMVar_hsa_circ_311739,RMVar_hsa_circ_270126,RMVar_hsa_circ_213692,RMVar_hsa_circ_213695,RMVar_hsa_circ_52895,RMVar_hsa_circ_307714,RMVar_hsa_circ_213696 90001 RMVar_ID_90001 Human_SNP_ID_701483189 m1A Human chr22 - 29832320 29832320 29832320 TTCCTTTCAGGAGGGTCACGCAGCACAATGCCAGCTCTGCCCCTGGACCAACTCCAGATCACCCA TTCCTTTCAGGAGGGTCACGCAGCACAATGCCGGCTCTGCCCCTGGACCAACTCCAGATCACCCA T C ASCC2 Ensembl:ENSG00000100325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:29832210..29832354;chr22:29832205..29832385 26863196 MeRIP-seq:(Medium) rs150260524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708940,Human_RBP_ID_14449738,Human_RBP_ID_19008893,Human_RBP_ID_23015594 Human_Splice_Rec_2152112,Human_Splice_Rec_2152113,Human_Splice_Rec_2152160,Human_Splice_Rec_2152161,Human_Splice_Rec_2152204,Human_Splice_Rec_2152205,Human_Splice_Rec_2152246,Human_Splice_Rec_2152247,Human_Splice_Rec_2152314,Human_Splice_Rec_2152315,Human_Splice_Rec_2152324,Human_Splice_Rec_2152325,Human_Splice_Rec_2152343,Human_Splice_Rec_2152354,Human_Splice_Rec_2152355,Human_Splice_Rec_2152369,Human_Splice_Rec_2152382,Human_Splice_Rec_2152383,Human_Splice_Rec_2152392,Human_Splice_Rec_2152393 RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213677,RMVar_hsa_circ_1091,RMVar_hsa_circ_41965,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_98815,RMVar_hsa_circ_213685,RMVar_hsa_circ_213686,RMVar_hsa_circ_213691,RMVar_hsa_circ_123113,RMVar_hsa_circ_311739,RMVar_hsa_circ_270126,RMVar_hsa_circ_213692,RMVar_hsa_circ_19767,RMVar_hsa_circ_213695,RMVar_hsa_circ_52895,RMVar_hsa_circ_307714,RMVar_hsa_circ_213696 90002 RMVar_ID_90002 Human_SNP_ID_701483190 m1A Human chr22 - 29832320 29832320 29832320 TTCCTTTCAGGAGGGTCACGCAGCACAATGCCAGCTCTGCCCCTGGACCAACTCCAGATCACCCA TTCCTTTCAGGAGGGTCACGCAGCACAATGCCCGCTCTGCCCCTGGACCAACTCCAGATCACCCA T G ASCC2 Ensembl:ENSG00000100325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:29832210..29832354;chr22:29832205..29832385 26863196 MeRIP-seq:(Medium) rs150260524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708940,Human_RBP_ID_14449738,Human_RBP_ID_19008893,Human_RBP_ID_23015594 Human_Splice_Rec_2152112,Human_Splice_Rec_2152113,Human_Splice_Rec_2152160,Human_Splice_Rec_2152161,Human_Splice_Rec_2152204,Human_Splice_Rec_2152205,Human_Splice_Rec_2152246,Human_Splice_Rec_2152247,Human_Splice_Rec_2152314,Human_Splice_Rec_2152315,Human_Splice_Rec_2152324,Human_Splice_Rec_2152325,Human_Splice_Rec_2152343,Human_Splice_Rec_2152354,Human_Splice_Rec_2152355,Human_Splice_Rec_2152369,Human_Splice_Rec_2152382,Human_Splice_Rec_2152383,Human_Splice_Rec_2152392,Human_Splice_Rec_2152393 RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213677,RMVar_hsa_circ_1091,RMVar_hsa_circ_41965,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_98815,RMVar_hsa_circ_213685,RMVar_hsa_circ_213686,RMVar_hsa_circ_213691,RMVar_hsa_circ_123113,RMVar_hsa_circ_311739,RMVar_hsa_circ_270126,RMVar_hsa_circ_213692,RMVar_hsa_circ_19767,RMVar_hsa_circ_213695,RMVar_hsa_circ_52895,RMVar_hsa_circ_307714,RMVar_hsa_circ_213696 90003 RMVar_ID_90003 Human_SNP_ID_701484672 m1A Human chr22 + 29838229 29838226 29838229 GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTT GCTCTGTGCCGCCGCCGCCGCCGCCGCCGC___CCACGGTGACAGCTCCCTGAGCGCCCGCACTT CCGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29838118..29838250;chr22:29838106..29838275 26863196 MeRIP-seq:(Medium) rs759597045 Functional Loss DEL dbSNP153 31..33 33 - - - 90004 RMVar_ID_90004 Human_SNP_ID_701484683 m1A Human chr22 + 29838229 29838229 29838229 GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTT GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGCCCACGGTGACAGCTCCCTGAGCGCCCGCACTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29838118..29838250;chr22:29838106..29838275 26863196 MeRIP-seq:(Medium) rs7289250 Functional Loss SNV dbSNP153 33..33 33 - - - 90005 RMVar_ID_90005 Human_SNP_ID_701484684 m1A Human chr22 + 29838229 29838229 29838229 GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTT GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGGCCACGGTGACAGCTCCCTGAGCGCCCGCACTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29838118..29838250;chr22:29838106..29838275 26863196 MeRIP-seq:(Medium) rs7289250 Functional Loss SNV dbSNP153 33..33 33 - - - 90006 RMVar_ID_90006 Human_SNP_ID_701484685 m1A Human chr22 + 29838229 29838229 29838229 GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTT GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGTCCACGGTGACAGCTCCCTGAGCGCCCGCACTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29838118..29838250;chr22:29838106..29838275 26863196 MeRIP-seq:(Medium) rs7289250 Functional Loss SNV dbSNP153 33..33 33 - - - 90007 RMVar_ID_90007 Human_SNP_ID_701484690 m1A Human chr22 + 29838232 29838232 29838232 CTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTTCCG CTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCCCGGTGACAGCTCCCTGAGCGCCCGCACTTCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr22:29838117..29838275;chr22:29838078..29838254 26863196 MeRIP-seq:(Medium) rs775814957 Functional Loss SNV dbSNP153 33..33 33 - - - 90008 RMVar_ID_90008 Human_SNP_ID_701484691 m1A Human chr22 + 29838232 29838232 29838232 CTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTTCCG CTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCGCGGTGACAGCTCCCTGAGCGCCCGCACTTCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr22:29838117..29838275;chr22:29838078..29838254 26863196 MeRIP-seq:(Medium) rs775814957 Functional Loss SNV dbSNP153 33..33 33 - - - 90009 RMVar_ID_90009 Human_SNP_ID_701495704 m1A Human chr22 - 29883354 29883354 29883354 GACGGAGGACGGGGATGGGGTTCTTACCGGGCAGCAGGACATGGCGAGGCCCTCCACGGCACAGT GACGGAGGACGGGGATGGGGTTCTTACCGGGCTGCAGGACATGGCGAGGCCCTCCACGGCACAGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:29883223..29883417 26863196 MeRIP-seq:(Medium) rs1473185445 Functional Loss SNV dbSNP153 33..33 33 - - - 90010 RMVar_ID_90010 Human_SNP_ID_701495760 m1A Human chr22 - 29883531 29883531 29883531 ACTCCCACACCCAGCGCCTCCCCCTGGCGGCGACAGCCGCCGGGGACGCCCCTCCCCGGGCCCCG ACTCCCACACCCAGCGCCTCCCCCTGGCGGCGTCAGCCGCCGGGGACGCCCCTCCCCGGGCCCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29883522..29883660 26863196 MeRIP-seq:(Medium) rs913077208 Functional Loss SNV dbSNP153 33..33 33 - - - 90011 RMVar_ID_90011 Human_SNP_ID_701582837 m1A Human chr22 + 30246750 30246748 30246750 CTTGGAGGAAACCTCAGATGCCGGCAGTTTTCAGAGGTTCATGCTCAAATGGGGAATTTGCCTGA CTTGGAGGAAACCTCAGATGCCGGCAGTTTT__GAGGTTCATGCTCAAATGGGGAATTTGCCTGA TCA T AC004264.1 Ensembl:ENSG00000268812 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30246699..30246804 26863196 MeRIP-seq:(Medium) rs780631044 Functional Loss DEL dbSNP153 32..33 33 - - - 90012 RMVar_ID_90012 Human_SNP_ID_701583228 m1A Human chr22 + 30248226 30248226 30248226 ACGAGCCCTGGTGCCTGCTGCCGTTCCCCACCACACACACACCCTGCTTTATCTACGCTCTTGCC ACGAGCCCTGGTGCCTGCTGCCGTTCCCCACCCCACACACACCCTGCTTTATCTACGCTCTTGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30248209..30248838 26863196 MeRIP-seq:(Medium) rs1007671339 Functional Loss SNV dbSNP153 33..33 33 - - - 90013 RMVar_ID_90013 Human_SNP_ID_701583229 m1A Human chr22 + 30248226 30248226 30248226 ACGAGCCCTGGTGCCTGCTGCCGTTCCCCACCACACACACACCCTGCTTTATCTACGCTCTTGCC ACGAGCCCTGGTGCCTGCTGCCGTTCCCCACCTCACACACACCCTGCTTTATCTACGCTCTTGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30248209..30248838 26863196 MeRIP-seq:(Medium) rs1007671339 Functional Loss SNV dbSNP153 33..33 33 - - - 90014 RMVar_ID_90014 Human_SNP_ID_701585761 m1A Human chr22 - 30257673 30257673 30257673 AGCGGCCTCGCCACGCAGCACTGGGCAGGGGCATCGGGCACAAGGACGCCCCCTCCCCACACCCC AGCGGCCTCGCCACGCAGCACTGGGCAGGGGCGTCGGGCACAAGGACGCCCCCTCCCCACACCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30257627..30257736 26863196 MeRIP-seq:(Medium) rs1023633659 Functional Loss SNV dbSNP153 33..33 33 - - - 90015 RMVar_ID_90015 Human_SNP_ID_701585813 m1A Human chr22 + 30257839 30257839 30257839 CGGCCTTAGGTGTTTTGACTCAGACCTGCCACAGGCCGTGTGCAGCACATCCAGCCTCCCCTTGT CGGCCTTAGGTGTTTTGACTCAGACCTGCCACTGGCCGTGTGCAGCACATCCAGCCTCCCCTTGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30257789..30257992 26863196 MeRIP-seq:(Medium) rs1000833674 Functional Loss SNV dbSNP153 33..33 33 - - - 90016 RMVar_ID_90016 Human_SNP_ID_701593354 m1A Human chr22 - 30286885 30286885 30286885 CCCACAGAACCGCTTCTGTGTCCTCACACTGGACCCTGAGACGCTTCCAGCCATCGCCACCACCC CCCACAGAACCGCTTCTGTGTCCTCACACTGGTCCCTGAGACGCTTCCAGCCATCGCCACCACCC T A CASTOR1,AC004997.1 Ensembl:ENSG00000239282,Ensembl:ENSG00000248751 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:30286810..30286910 32194978 MeRIP-seq:(Medium) rs143253536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2152730,Human_Splice_Rec_2152731,Human_Splice_Rec_2152746,Human_Splice_Rec_2152747,Human_Splice_Rec_2152766,Human_Splice_Rec_2152767,Human_Splice_Rec_2152778,Human_Splice_Rec_2152788,Human_Splice_Rec_2152789,Human_Splice_Rec_2152796,Human_Splice_Rec_2152797,Human_Splice_Rec_2152806,Human_Splice_Rec_2152840,Human_Splice_Rec_2152841,Human_Splice_Rec_2152866,Human_Splice_Rec_2152867,Human_Splice_Rec_2152890,Human_Splice_Rec_2152891,Human_Splice_Rec_2152912,Human_Splice_Rec_2152913,Human_Splice_Rec_2152934,Human_Splice_Rec_2152935 RMVar_hsa_circ_72155,RMVar_hsa_circ_102554,RMVar_hsa_circ_213735 90017 RMVar_ID_90017 Human_SNP_ID_701593523 m1A Human chr22 + 30287259 30287259 30287259 GGTAAATGTCGAACTCCTGGGCCAGCGTGTGGATCACCACGGACAGGTCCTGCTCCCGCACCTGG GGTAAATGTCGAACTCCTGGGCCAGCGTGTGGGTCACCACGGACAGGTCCTGCTCCCGCACCTGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:30287209..30287310 32194978 MeRIP-seq:(Medium) rs1438851474 Functional Loss SNV dbSNP153 33..33 33 - - - 90018 RMVar_ID_90018 Human_SNP_ID_701602922 m1A Human chr22 - 30326831 30326831 30326831 GAGAATGGGCCGCGCGCGCCCGCGGCCGGGGAAAGCCTGTCGGGAACCCGGGAGAGCCTGGCCCA GAGAATGGGCCGCGCGCGCCCGCGGCCGGGGATAGCCTGTCGGGAACCCGGGAGAGCCTGGCCCA T A TBC1D10A Ensembl:ENSG00000099992 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30326793..30326884 26863196 MeRIP-seq:(Medium) rs777107532 Functional Loss SNV dbSNP153 33..33 33 - - - 90019 RMVar_ID_90019 Human_SNP_ID_701602923 m1A Human chr22 - 30326831 30326831 30326831 GAGAATGGGCCGCGCGCGCCCGCGGCCGGGGAAAGCCTGTCGGGAACCCGGGAGAGCCTGGCCCA GAGAATGGGCCGCGCGCGCCCGCGGCCGGGGAGAGCCTGTCGGGAACCCGGGAGAGCCTGGCCCA T C TBC1D10A Ensembl:ENSG00000099992 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30326793..30326884 26863196 MeRIP-seq:(Medium) rs777107532 Functional Loss SNV dbSNP153 33..33 33 - - - 90020 RMVar_ID_90020 Human_SNP_ID_701602942 m1A Human chr22 + 30326858 30326858 30326858 AGGCTTTCCCCGGCCGCGGGCGCGCGCGGCCCATTCTCTCCGTTGCTCTTCGCCATCCCAGCCGC AGGCTTTCCCCGGCCGCGGGCGCGCGCGGCCCGTTCTCTCCGTTGCTCTTCGCCATCCCAGCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30326807..30326897 26863196 MeRIP-seq:(Medium) rs748569575 Functional Loss SNV dbSNP153 33..33 33 - - - 90021 RMVar_ID_90021 Human_SNP_ID_701602952 m1A Human chr22 + 30326880 30326880 30326880 CGCGCGGCCCATTCTCTCCGTTGCTCTTCGCCATCCCAGCCGCGCCCGCCGCCTGAGCTCCAGCG CGCGCGGCCCATTCTCTCCGTTGCTCTTCGCCGTCCCAGCCGCGCCCGCCGCCTGAGCTCCAGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30326705..30326888 26863196 MeRIP-seq:(Medium) rs1308192121 Functional Loss SNV dbSNP153 33..33 33 - - - 90022 RMVar_ID_90022 Human_SNP_ID_701604414 m1A Human chr22 + 30332442 30332442 30332442 CTATTTCATAGTGTGGTCTGGTGGAGCAGAGCAGTGTGGTCCCCAGGAAGGGATGAGCTGCTTTG CTATTTCATAGTGTGGTCTGGTGGAGCAGAGCCGTGTGGTCCCCAGGAAGGGATGAGCTGCTTTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:30332361..30332442 32194978 MeRIP-seq:(Medium) rs527721939 Functional Loss SNV dbSNP153 33..33 33 - - - 90023 RMVar_ID_90023 Human_SNP_ID_701604831 m1A Human chr22 - 30334458 30334458 30334458 TTTGTTTCGCTCTTACTCAGTTTGGGAATTCAAATTGTCCTGCAGAGGTTCATTCCCCTGACCCT TTTGTTTCGCTCTTACTCAGTTTGGGAATTCAGATTGTCCTGCAGAGGTTCATTCCCCTGACCCT T C SF3A1 Ensembl:ENSG00000099995 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1438968887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65941,Human_RBP_ID_577995,Human_RBP_ID_1609931,Human_RBP_ID_3671070,Human_RBP_ID_7074275,Human_RBP_ID_8548334,Human_RBP_ID_17285503,Human_RBP_ID_17398732,Human_RBP_ID_17514707,Human_RBP_ID_18787078,Human_RBP_ID_18952915,Human_RBP_ID_20747454,Human_RBP_ID_23942712 90024 RMVar_ID_90024 Human_SNP_ID_701604832 m1A Human chr22 - 30334458 30334458 30334458 TTTGTTTCGCTCTTACTCAGTTTGGGAATTCAAATTGTCCTGCAGAGGTTCATTCCCCTGACCCT TTTGTTTCGCTCTTACTCAGTTTGGGAATTCACATTGTCCTGCAGAGGTTCATTCCCCTGACCCT T G SF3A1 Ensembl:ENSG00000099995 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1438968887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65941,Human_RBP_ID_577995,Human_RBP_ID_1609931,Human_RBP_ID_3671070,Human_RBP_ID_7074275,Human_RBP_ID_8548334,Human_RBP_ID_17285503,Human_RBP_ID_17398732,Human_RBP_ID_17514707,Human_RBP_ID_18787078,Human_RBP_ID_18952915,Human_RBP_ID_20747454,Human_RBP_ID_23942712 90025 RMVar_ID_90025 Human_SNP_ID_701605466 m1A Human chr22 - 30337058 30337058 30337058 CCTCCAAAAAACTGAAGACAGAGGACAGCCTCATGCCAGAGGAGGAGTTCCTGCGCAGAAACAAG CCTCCAAAAAACTGAAGACAGAGGACAGCCTCCTGCCAGAGGAGGAGTTCCTGCGCAGAAACAAG T G SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:30335661..30339082 32194978 MeRIP-seq:(Medium) rs1184038547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246507,Human_RBP_ID_578001,Human_RBP_ID_7074285,Human_RBP_ID_8208608,Human_RBP_ID_8548338,Human_RBP_ID_17399783,Human_RBP_ID_26345293 Human_Splice_Rec_2153081 90026 RMVar_ID_90026 Human_SNP_ID_701605495 m1A Human chr22 + 30337125 30337125 30337125 GGCTCATCTTCCATGGGAGGTGGGGGATGCACAGGGGGCATTGGGGCTGGAGCTGGGACAGGTGC GGCTCATCTTCCATGGGAGGTGGGGGATGCACCGGGGGCATTGGGGCTGGAGCTGGGACAGGTGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:30337076..30337175 26863196 MeRIP-seq:(Medium) rs1406726772 Functional Loss SNV dbSNP153 33..33 33 - - - 90027 RMVar_ID_90027 Human_SNP_ID_701605724 m1A Human chr22 - 30337811 30337811 30337811 CCCCCAATGGCATCTGTGGTCCGGCTGCCCCCAGGCTCAGTGATCGCCCCCATGCCGCCCATCAT CCCCCAATGGCATCTGTGGTCCGGCTGCCCCCTGGCTCAGTGATCGCCCCCATGCCGCCCATCAT T A SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30337037..30340431 26863196 MeRIP-seq:(Medium) rs754977910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_578002,Human_RBP_ID_7074286,Human_RBP_ID_8862629,Human_RBP_ID_17285507,Human_RBP_ID_17399785,Human_RBP_ID_17515807,Human_RBP_ID_18194329,Human_RBP_ID_23942714,Human_RBP_ID_27035156 Human_Splice_Rec_2153078,Human_Splice_Rec_2153092,Human_Splice_Rec_2153100 90028 RMVar_ID_90028 Human_SNP_ID_701606029 m1A Human chr22 - 30338781 30338781 30338781 CACTTCAGTGCCCCGACCACCCACAGTAAGCCAGCATCTACCCTGGAACTGACTTTTTTAGAGCT CACTTCAGTGCCCCGACCACCCACAGTAAGCCGGCATCTACCCTGGAACTGACTTTTTTAGAGCT T C SF3A1 Ensembl:ENSG00000099995 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:30338776..30338825 26863196 MeRIP-seq:(Medium) rs374253846 Functional Loss SNV dbSNP153 33..33 33 - - - 90029 RMVar_ID_90029 Human_SNP_ID_701606121 m1A Human chr22 - 30339188 30339188 30339188 GGCTGAGCGGCGTACTGACATCTTCGGTGTAGAGGAAACAGCCATTGGTAAGAAGATCGGTGAGG GGCTGAGCGGCGTACTGACATCTTCGGTGTAGGGGAAACAGCCATTGGTAAGAAGATCGGTGAGG T C SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30338951..30339275 26863196 MeRIP-seq:(Medium) rs1414031201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782156,Human_RBP_ID_1028931,Human_RBP_ID_1609944,Human_RBP_ID_1941545,Human_RBP_ID_3671072,Human_RBP_ID_7074290,Human_RBP_ID_8862632,Human_RBP_ID_9300669,Human_RBP_ID_9392163,Human_RBP_ID_14452463,Human_RBP_ID_17514710,Human_RBP_ID_27821222 Human_Splice_Rec_2153074,Human_Splice_Rec_2153075,Human_Splice_Rec_2153089,Human_Splice_Rec_2153102,Human_Splice_Rec_2153103,Human_Splice_Rec_2153106 90030 RMVar_ID_90030 Human_SNP_ID_701606352 m1A Human chr22 - 30340146 30340146 30340146 GGAGAGCCCATGGTAGTCTCCGAATTACAGCCATCTTCTTCTAAGCAAACATAGAAAGCAACAAT GGAGAGCCCATGGTAGTCTCCGAATTACAGCCGTCTTCTTCTAAGCAAACATAGAAAGCAACAAT T C SF3A1 Ensembl:ENSG00000099995 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30340144..30340424 26863196 MeRIP-seq:(Medium) rs1444565668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5389064 90031 RMVar_ID_90031 Human_SNP_ID_701606365 m1A Human chr22 - 30340179 30340179 30340179 GAGGTGTACGCACCAGGTGAGGTGGGGGTTCCAGGAGAGCCCATGGTAGTCTCCGAATTACAGCC GAGGTGTACGCACCAGGTGAGGTGGGGGTTCCGGGAGAGCCCATGGTAGTCTCCGAATTACAGCC T C SF3A1 Ensembl:ENSG00000099995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:30340176..30340225;chr22:30340176..30340250 26863196 MeRIP-seq:(Medium) rs1400109448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5389064,Human_RBP_ID_19111840 90032 RMVar_ID_90032 Human_SNP_ID_701606409 m1A Human chr22 + 30340343 30340343 30340343 GATCTTCTCCCCAGTAATGGGGGACACAAGATACTCATCTGGAGCAGGGGCTGGAGGCAAGGGCT GATCTTCTCCCCAGTAATGGGGGACACAAGATGCTCATCTGGAGCAGGGGCTGGAGGCAAGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30340293..30340413 26863196 MeRIP-seq:(Medium) rs1352965421 Functional Loss SNV dbSNP153 33..33 33 - - - 90033 RMVar_ID_90033 Human_SNP_ID_701606558 m1A Human chr22 - 30340793 30340790 30340793 CTTTGCTTTTCAGGGTTCAGATGATGAAGAAGAAGGGCAGAAAGTGCCCCCACCCCCAGAGACAC CTTTGCTTTTCAGGGTTCAGATGATGAAGAAG___GGCAGAAAGTGCCCCCACCCCCAGAGACAC CCTT C SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30340667..30340843 26863196 MeRIP-seq:(Medium) rs1449715093 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_64919,Human_RBP_ID_1609950,Human_RBP_ID_8548343,Human_RBP_ID_17989190,Human_RBP_ID_26345297 Human_Splice_Rec_2153070,Human_Splice_Rec_2153071,Human_Splice_Rec_2153094,Human_Splice_Rec_2153095 RMVar_hsa_circ_101369,RMVar_hsa_circ_106607,RMVar_hsa_circ_213741,RMVar_hsa_circ_97623,RMVar_hsa_circ_213742,RMVar_hsa_circ_213740 90034 RMVar_ID_90034 Human_SNP_ID_701606824 m1A Human chr22 + 30341776 30341776 30341776 TCCGCCTTCTCCTGTTTGTCATCCTCCTCATCAGACTCGACCTCCATCTCAACTTCCTCACTCTC TCCGCCTTCTCCTGTTTGTCATCCTCCTCATCGGACTCGACCTCCATCTCAACTTCCTCACTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30341662..30341912 26863196 MeRIP-seq:(Medium) rs1168790638 Functional Loss SNV dbSNP153 33..33 33 - - - 90035 RMVar_ID_90035 Human_SNP_ID_701606969 m1A Human chr22 - 30342259 30342259 30342259 GGAGAAGGAGAAGGAGCGGGTGGCCTATGCTCAGATCGACTGGCATGATTTTGTGGTGGTGGAAA GGAGAAGGAGAAGGAGCGGGTGGCCTATGCTCGGATCGACTGGCATGATTTTGTGGTGGTGGAAA T C SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30342184..30342375 26863196 MeRIP-seq:(Medium) rs1225863671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_211720,Human_RBP_ID_245697,Human_RBP_ID_781025,Human_RBP_ID_833298,Human_RBP_ID_930770,Human_RBP_ID_1028938,Human_RBP_ID_1068878,Human_RBP_ID_3963147,Human_RBP_ID_4692243,Human_RBP_ID_5148993,Human_RBP_ID_8865931,Human_RBP_ID_9300341,Human_RBP_ID_9392165,Human_RBP_ID_17701811,Human_RBP_ID_19007862,Human_RBP_ID_26345299,Human_RBP_ID_27821603 Human_Splice_Rec_2153066,Human_Splice_Rec_2153067,Human_Splice_Rec_2153112 RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 90036 RMVar_ID_90036 Human_SNP_ID_701610145 m1A Human chr22 - 30354328 30354328 30354328 GGCTGTGGGCAGTTGTTTTTGACTTTGTCAAGAGCACTTAAAATGAATGGGGACCAGATGGGAGG GGCTGTGGGCAGTTGTTTTTGACTTTGTCAAGGGCACTTAAAATGAATGGGGACCAGATGGGAGG T C SF3A1 Ensembl:ENSG00000099995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30354324..30354571 26863196 MeRIP-seq:(Medium) rs1041041827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 90037 RMVar_ID_90037 Human_SNP_ID_701610880 m1A Human chr22 - 30356796 30356796 30356796 CACCGAGGCGGACTGGCAGCCCTGAGCGTCGCAGTCATGCCGGCCGGACCCGTGCAGGCGGTGCC CACCGAGGCGGACTGGCAGCCCTGAGCGTCGCGGTCATGCCGGCCGGACCCGTGCAGGCGGTGCC T C SF3A1 Ensembl:ENSG00000099995 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:30356747..30356847 32194978 MeRIP-seq:(Medium) rs1228667000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245701,Human_RBP_ID_4708558,Human_RBP_ID_5202968,Human_RBP_ID_5504540,Human_RBP_ID_8865933,Human_RBP_ID_27492927 Human_Splice_Rec_2153057,Human_Splice_Rec_2153087,Human_Splice_Rec_2153107,Human_Splice_Rec_2153117,Human_Splice_Rec_2153121 RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 90038 RMVar_ID_90038 Human_SNP_ID_701610902 m1A Human chr22 - 30356840 30356840 30356840 CTGACCGAGCGGGGAGGCTGTCTTGAGGCGGCACCGCTCACCGACACCGAGGCGGACTGGCAGCC CTGACCGAGCGGGGAGGCTGTCTTGAGGCGGCTCCGCTCACCGACACCGAGGCGGACTGGCAGCC T A SF3A1 Ensembl:ENSG00000099995 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30356726..30356900 26863196 MeRIP-seq:(Medium) rs1289259756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708559,Human_RBP_ID_8865687,Human_RBP_ID_9300343,Human_RBP_ID_26822385 RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 90039 RMVar_ID_90039 Human_SNP_ID_701610903 m1A Human chr22 - 30356840 30356840 30356840 CTGACCGAGCGGGGAGGCTGTCTTGAGGCGGCACCGCTCACCGACACCGAGGCGGACTGGCAGCC CTGACCGAGCGGGGAGGCTGTCTTGAGGCGGCGCCGCTCACCGACACCGAGGCGGACTGGCAGCC T C SF3A1 Ensembl:ENSG00000099995 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30356726..30356900 26863196 MeRIP-seq:(Medium) rs1289259756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708559,Human_RBP_ID_8865687,Human_RBP_ID_9300343,Human_RBP_ID_26822385 RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 90040 RMVar_ID_90040 Human_SNP_ID_701610906 m1A Human chr22 + 30356852 30356852 30356852 GCCTCGGTGTCGGTGAGCGGTGCCGCCTCAAGACAGCCTCCCCGCTCGGTCAGTACGACGAGCTC GCCTCGGTGTCGGTGAGCGGTGCCGCCTCAAGTCAGCCTCCCCGCTCGGTCAGTACGACGAGCTC A T CCDC157 Ensembl:ENSG00000187860 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30356677..30356900 26863196 MeRIP-seq:(Medium) rs1463077085 Functional Loss SNV dbSNP153 33..33 33 - - - 90041 RMVar_ID_90041 Human_SNP_ID_701614461 m1A Human chr22 + 30370831 30370831 30370831 GGAGGCTGAAGGGCAGAAGGATGGCCTGAGGAAGCAGGCGGGCAAGCTGGAGCAGGCGCTGAAAC GGAGGCTGAAGGGCAGAAGGATGGCCTGAGGAGGCAGGCGGGCAAGCTGGAGCAGGCGCTGAAAC A G CCDC157 Ensembl:ENSG00000187860 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30370782..30370970 26863196 MeRIP-seq:(Medium) rs563598346 Functional Loss SNV dbSNP153 33..33 33 - - - 90042 RMVar_ID_90042 Human_SNP_ID_701614817 m1A Human chr22 - 30372056 30372056 30372056 CTGGGCCTTTGCCTCTGCAGCATTAAGTGGACATGGGATGGGGTAGGGCAGGGGAGCGCTGTACT CTGGGCCTTTGCCTCTGCAGCATTAAGTGGACGTGGGATGGGGTAGGGCAGGGGAGCGCTGTACT T C RNF215 Ensembl:ENSG00000099999 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30372053..30372297 26863196 MeRIP-seq:(Medium) rs1040623214 Functional Loss SNV dbSNP153 33..33 33 - - - 90043 RMVar_ID_90043 Human_SNP_ID_701619454 m1A Human chr22 + 30387117 30387114 30387117 CGCCCTCCAGGACCAGAGCGTCCTGGCGCGGCAGTCTCACGTCCACCCGCACGGCGCGGGCTCCG CGCCCTCCAGGACCAGAGCGTCCTGGCGCG___GTCTCACGTCCACCCGCACGGCGCGGGCTCCG GGCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30387004..30387177 26863196 MeRIP-seq:(Medium) rs1569200210 Functional Loss DEL dbSNP153 31..33 33 - - - 90044 RMVar_ID_90044 Human_SNP_ID_701619543 m1A Human chr22 + 30387288 30387288 30387288 GAGGCGGCGGCGGAGGCGGCGGCGGCGATCTCAGCGCGGGGCGAGCGGCGGGGCCCATGGCCGGA GAGGCGGCGGCGGAGGCGGCGGCGGCGATCTCGGCGCGGGGCGAGCGGCGGGGCCCATGGCCGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:30387240..30387389;chr22:30387258..30387358 26863196 MeRIP-seq:(Medium) rs1428948535 Functional Loss SNV dbSNP153 33..33 33 - - - 90045 RMVar_ID_90045 Human_SNP_ID_701628335 m1A Human chr22 - 30422758 30422758 30422758 TCTCCCCGGCAGCTGACTTCCCTGAAGTGTTAAGTCCCAATCTTTCACCCTTTTCTAATTTTTTT TCTCCCCGGCAGCTGACTTCCCTGAAGTGTTACGTCCCAATCTTTCACCCTTTTCTAATTTTTTT T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:30422756..30422838 26863410 MeRIP-seq:(Medium) rs1203197835 Functional Loss SNV dbSNP153 33..33 33 - - - 90046 RMVar_ID_90046 Human_SNP_ID_701629226 m1A Human chr22 + 30425827 30425827 30425827 CGGCCGGGCAGACCCAAGTGCCGGCGGCGGAGACTGCAGTGGAGCCAGTACCGGCTGTAGTGGCC CGGCCGGGCAGACCCAAGTGCCGGCGGCGGAGGCTGCAGTGGAGCCAGTACCGGCTGTAGTGGCC A G AC004832.3,MTFP1 Ensembl:ENSG00000249590,Ensembl:ENSG00000242114 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30425776..30427291 26863196 MeRIP-seq:(Medium) rs891214368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10652,Human_RBP_ID_4708146,Human_RBP_ID_19008909 90047 RMVar_ID_90047 Human_SNP_ID_701629233 m1A Human chr22 - 30425850 30425850 30425850 CATGACTCTCCCGCCACGGCCCCGGCCACTACAGCCGGTACTGGCTCCACTGCAGTCTCCGCCGC CATGACTCTCCCGCCACGGCCCCGGCCACTACCGCCGGTACTGGCTCCACTGCAGTCTCCGCCGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:30425801..30425953 26863196 MeRIP-seq:(Medium) rs913374197 Functional Loss SNV dbSNP153 33..33 33 - - - 90048 RMVar_ID_90048 Human_SNP_ID_701629984 m1A Human chr22 - 30428453 30428453 30428453 GAGTCCAGGAGGAAATCCACCGACCTGTAGGGAGTGGAAGGGTGGTGAGCAGGTGACCAAGGGTG GAGTCCAGGAGGAAATCCACCGACCTGTAGGGGGTGGAAGGGTGGTGAGCAGGTGACCAAGGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30428451..30428550 26863196 MeRIP-seq:(Medium) rs763654270 Functional Loss SNV dbSNP153 33..33 33 - - - 90049 RMVar_ID_90049 Human_SNP_ID_701668903 m1A Human chr22 - 30579186 30579186 30579186 GGAGGAAGATGCAGAGGCTGGTTCAGAAAAGGAGGAAGAGGCCCGGCTGGCAGCCCTGGAAGAGC GGAGGAAGATGCAGAGGCTGGTTCAGAAAAGGGGGAAGAGGCCCGGCTGGCAGCCCTGGAAGAGC T C PES1 Ensembl:ENSG00000100029 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:30578826..30579331;chr22:30576765..30579325 26863196 MeRIP-seq:(Medium) rs1015340574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64942,Human_RBP_ID_578088,Human_RBP_ID_3962308,Human_RBP_ID_5389074,Human_RBP_ID_7074482,Human_RBP_ID_9392172,Human_RBP_ID_17659996,Human_RBP_ID_17671116,Human_RBP_ID_18194331,Human_RBP_ID_18413091,Human_RBP_ID_23942834,Human_RBP_ID_26345306,Human_RBP_ID_27821226 Human_Splice_Rec_2153945,Human_Splice_Rec_2153977,Human_Splice_Rec_2153983,Human_Splice_Rec_2154015,Human_Splice_Rec_2154045,Human_Splice_Rec_2154073 Human_miRNA_ID_2398724 RMVar_hsa_circ_89543,RMVar_hsa_circ_117272,RMVar_hsa_circ_105098,RMVar_hsa_circ_44901,RMVar_hsa_circ_213751,RMVar_hsa_circ_213753,RMVar_hsa_circ_79229,RMVar_hsa_circ_213752,RMVar_hsa_circ_213750 90050 RMVar_ID_90050 Human_SNP_ID_701669113 m1A Human chr22 + 30579828 30579828 30579828 GTGGAACGTAATCTCCTTCCTTCTCGGTCACAAAGGGTGAAAGGTGTGGGGGCAGCTGCACCCCA GTGGAACGTAATCTCCTTCCTTCTCGGTCACAGAGGGTGAAAGGTGTGGGGGCAGCTGCACCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:30579767..30579966 32194978 MeRIP-seq:(Medium) rs758299916 Functional Loss SNV dbSNP153 33..33 33 - - - 90051 RMVar_ID_90051 Human_SNP_ID_701669226 m1A Human chr22 - 30580122 30580122 30580122 GGACAAATCTTTGTGCATTGGGGCCACCTATGACGTCACAGACTCCCGCATCACCCATCAGATTG GGACAAATCTTTGTGCATTGGGGCCACCTATGTCGTCACAGACTCCCGCATCACCCATCAGATTG T A PES1 Ensembl:ENSG00000100029 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30580038..30580200 26863196 MeRIP-seq:(Medium) rs140230829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64947,Human_RBP_ID_1028953,Human_RBP_ID_1201297,Human_RBP_ID_3671106,Human_RBP_ID_7074488,Human_RBP_ID_8548409,Human_RBP_ID_8862659,Human_RBP_ID_9392175,Human_RBP_ID_14453639,Human_RBP_ID_17984578 Human_Splice_Rec_2153940,Human_Splice_Rec_2153941,Human_Splice_Rec_2153972,Human_Splice_Rec_2153973,Human_Splice_Rec_2154010,Human_Splice_Rec_2154011,Human_Splice_Rec_2154040,Human_Splice_Rec_2154041,Human_Splice_Rec_2154068,Human_Splice_Rec_2154069 RMVar_hsa_circ_89543,RMVar_hsa_circ_117272,RMVar_hsa_circ_29528,RMVar_hsa_circ_44901,RMVar_hsa_circ_213751,RMVar_hsa_circ_79229,RMVar_hsa_circ_213752,RMVar_hsa_circ_213750,RMVar_hsa_circ_51657 90052 RMVar_ID_90052 Human_SNP_ID_701669478 m1A Human chr22 + 30581003 30581003 30581003 CCCCTCCCAGCCCTCCTGCCAGAAGGCAGTGCAGTGCTCACCCCATCGGTGGGAAACTCATCCAC CCCCTCCCAGCCCTCCTGCCAGAAGGCAGTGCGGTGCTCACCCCATCGGTGGGAAACTCATCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30581001..30581125 26863196 MeRIP-seq:(Medium) rs773937656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213754 90053 RMVar_ID_90053 Human_SNP_ID_701669594 m1A Human chr22 - 30581328 30581328 30581328 GCGTTGGACTCCGAGAGTTGTATGGAGGTGAGAGGCTCCAGGAGCATCATCCGGCATCTCCCAAG GCGTTGGACTCCGAGAGTTGTATGGAGGTGAGGGGCTCCAGGAGCATCATCCGGCATCTCCCAAG T C PES1 Ensembl:ENSG00000100029 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30581326..30581425 26863196 MeRIP-seq:(Medium) rs776381134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14453646,Human_RBP_ID_19113052 Human_Splice_Rec_2153934,Human_Splice_Rec_2153966,Human_Splice_Rec_2154004,Human_Splice_Rec_2154034,Human_Splice_Rec_2154062,Human_Splice_Rec_2154090 RMVar_hsa_circ_89543,RMVar_hsa_circ_117272,RMVar_hsa_circ_44901,RMVar_hsa_circ_213751,RMVar_hsa_circ_79229,RMVar_hsa_circ_213752,RMVar_hsa_circ_213750 90054 RMVar_ID_90054 Human_SNP_ID_701669696 m1A Human chr22 + 30581578 30581578 30581578 GTTGAGCAACTGGTAAAGGCGGAAGTTGACAAAGCCCAGCAGCGTGGTGTAGAACTCGGTGAAGG GTTGAGCAACTGGTAAAGGCGGAAGTTGACAATGCCCAGCAGCGTGGTGTAGAACTCGGTGAAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30581497..30581625 26863196 MeRIP-seq:(Medium) rs754653033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213754 90055 RMVar_ID_90055 Human_SNP_ID_701672463 m1A Human chr22 - 30591844 30591844 30591844 CTCCCTGTACGCGCGGCCCTAGTCGGCTCCTCAACGTGGAGCGATGGGAGGCCTTGAGAAGAAGA CTCCCTGTACGCGCGGCCCTAGTCGGCTCCTCGACGTGGAGCGATGGGAGGCCTTGAGAAGAAGA T C PES1 Ensembl:ENSG00000100029 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30591752..30591847 26863196 MeRIP-seq:(Medium) rs750187668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708565,Human_RBP_ID_5473424,Human_RBP_ID_26822396 Human_Splice_Rec_2153921,Human_Splice_Rec_2154021,Human_Splice_Rec_2154049,Human_Splice_Rec_2154077,Human_Splice_Rec_2154097,Human_Splice_Rec_2154105 RMVar_hsa_circ_38331,RMVar_hsa_circ_49748 90056 RMVar_ID_90056 Human_SNP_ID_701672469 m1A Human chr22 + 30591854 30591854 30591854 AAGGCCTCCCATCGCTCCACGTTGAGGAGCCGACTAGGGCCGCGCGTACAGGGAGCTCCACTTCC AAGGCCTCCCATCGCTCCACGTTGAGGAGCCGTCTAGGGCCGCGCGTACAGGGAGCTCCACTTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:30589176..30591900 26863196 MeRIP-seq:(Medium) rs1344499727 Functional Loss SNV dbSNP153 33..33 33 - - - 90057 RMVar_ID_90057 Human_SNP_ID_701690062 m1A Human chr22 - 30637043 30637043 30637043 ACTTACTTTGCTGAACCGACTTGAGTCCGCGGAGGCAGGTGGCTGCGAGCAGGAAGCCACAGCCG ACTTACTTTGCTGAACCGACTTGAGTCCGCGGCGGCAGGTGGCTGCGAGCAGGAAGCCACAGCCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:30636996..30646774 32194978 MeRIP-seq:(Medium) rs761373533 Functional Loss SNV dbSNP153 33..33 33 - - - 90058 RMVar_ID_90058 Human_SNP_ID_701708972 m1A Human chr22 - 30709622 30709621 30709623 AATCTCAGCACTTCAGGAGGCTGAGGCAGGAGAACTGGTTGAATCTGGGAGGTGGAGTTTGCAGT AATCTCAGCACTTCAGGAGGCTGAGGCAGGA__ACTGGTTGAATCTGGGAGGTGGAGTTTGCAGT TTC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:30709619..30709746 26863196 MeRIP-seq:(Medium) rs1389056029 Functional Loss DEL dbSNP153 32..33 33 - - - 90059 RMVar_ID_90059 Human_SNP_ID_701719458 m1A Human chr22 - 30753236 30753233 30753237 TCCTATCCCCACACCCCACCTCCAGCCACCCCAAGACACTGAGGGCCTCCTACCTTACACTGTGC TCCTATCCCCACACCCCACCTCCAGCCACCC____ACACTGAGGGCCTCCTACCTTACACTGTGC TCTTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30753218..30753370 26863196 MeRIP-seq:(Medium) rs910289909 Functional Loss DEL dbSNP153 32..35 33 - - - 90060 RMVar_ID_90060 Human_SNP_ID_701720141 m1A Human chr22 + 30756534 30756534 30756534 GACCAATACGGTGAAACCCCGTCTCTAGTAAAAATACAAAAATTAGCTGGGCATGGTGGCGCACG GACCAATACGGTGAAACCCCGTCTCTAGTAAATATACAAAAATTAGCTGGGCATGGTGGCGCACG A T OSBP2 Ensembl:ENSG00000184792 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30756518..30756602 26863196 MeRIP-seq:(Medium) rs1043391134 Functional Loss SNV dbSNP153 33..33 33 - - - 90061 RMVar_ID_90061 Human_SNP_ID_701730747 m1A Human chr22 + 30802824 30802824 30802824 CGGGCGGTGGGGAGGAGGCTGGAGGAATGAGGACGCAGCACGGCGCGCCCTTGCAGCGCTCAGGC CGGGCGGTGGGGAGGAGGCTGGAGGAATGAGGCCGCAGCACGGCGCGCCCTTGCAGCGCTCAGGC A C OSBP2 Ensembl:ENSG00000184792 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30802804..30802983 26863196 MeRIP-seq:(Medium) rs1314446319 Functional Loss SNV dbSNP153 33..33 33 - - - 90062 RMVar_ID_90062 Human_SNP_ID_701749462 m1A Human chr22 + 30881704 30881704 30881704 GCCCAGCTCAGCATTCTGAGAACAGCAGGGCCACGCCAGGCGCCTGCCTCTCCCCACAGCACAGC GCCCAGCTCAGCATTCTGAGAACAGCAGGGCCGCGCCAGGCGCCTGCCTCTCCCCACAGCACAGC A G OSBP2 Ensembl:ENSG00000184792 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:30881694..30881789 26863196 MeRIP-seq:(Medium) rs899924044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708566 Human_Splice_Rec_2154453,Human_Splice_Rec_2154461,Human_Splice_Rec_2154473,Human_Splice_Rec_2154495 RMVar_hsa_circ_38141,RMVar_hsa_circ_48897,RMVar_hsa_circ_310727,RMVar_hsa_circ_213764,RMVar_hsa_circ_6720 90063 RMVar_ID_90063 Human_SNP_ID_701750812 m1A Human chr22 + 30887475 30887475 30887475 GGAACTAGCAGAGATACACAGTCGGAAATGGCAGCGGGCACTGCAGTATGAGCAGGAGCAGCGCG GGAACTAGCAGAGATACACAGTCGGAAATGGCGGCGGGCACTGCAGTATGAGCAGGAGCAGCGCG A G OSBP2 Ensembl:ENSG00000184792 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30887415..30887500 26863196 MeRIP-seq:(Medium) rs772099698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26345884 Human_Splice_Rec_2154248,Human_Splice_Rec_2154274,Human_Splice_Rec_2154300,Human_Splice_Rec_2154326,Human_Splice_Rec_2154352,Human_Splice_Rec_2154384,Human_Splice_Rec_2154388,Human_Splice_Rec_2154422,Human_Splice_Rec_2154432,Human_Splice_Rec_2154454,Human_Splice_Rec_2154462,Human_Splice_Rec_2154474,Human_Splice_Rec_2154496 RMVar_hsa_circ_38141,RMVar_hsa_circ_48897,RMVar_hsa_circ_310727,RMVar_hsa_circ_213764,RMVar_hsa_circ_6720 90064 RMVar_ID_90064 Human_SNP_ID_701750835 m1A Human chr22 + 30887511 30887511 30887511 GGCACTGCAGTATGAGCAGGAGCAGCGCGTGCACTTGGAGGAAACCATTGAGCAGCTGGCGAAGC GGCACTGCAGTATGAGCAGGAGCAGCGCGTGCTCTTGGAGGAAACCATTGAGCAGCTGGCGAAGC A T OSBP2 Ensembl:ENSG00000184792 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:30887470..30887599 26863196 MeRIP-seq:(Medium) rs760619396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26345884 Human_Splice_Rec_2154248,Human_Splice_Rec_2154274,Human_Splice_Rec_2154300,Human_Splice_Rec_2154326,Human_Splice_Rec_2154352,Human_Splice_Rec_2154384,Human_Splice_Rec_2154388,Human_Splice_Rec_2154422,Human_Splice_Rec_2154432,Human_Splice_Rec_2154454,Human_Splice_Rec_2154462,Human_Splice_Rec_2154474,Human_Splice_Rec_2154496 RMVar_hsa_circ_38141,RMVar_hsa_circ_48897,RMVar_hsa_circ_310727,RMVar_hsa_circ_213764,RMVar_hsa_circ_6720 90065 RMVar_ID_90065 Human_SNP_ID_701755791 m1A Human chr22 + 30906001 30906001 30906001 GGCCAATACCGAGAAGCAGCGGCTGGAGGAGAAGCAGCGCCTGTCGCGGCGCCGGCGGCTGGAGG GGCCAATACCGAGAAGCAGCGGCTGGAGGAGACGCAGCGCCTGTCGCGGCGCCGGCGGCTGGAGG A C OSBP2 Ensembl:ENSG00000184792 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr22:30905950..30906075;chr22:30905951..30906433 26863196 MeRIP-seq:(Medium) rs906348599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2154267,Human_Splice_Rec_2154293,Human_Splice_Rec_2154319,Human_Splice_Rec_2154345,Human_Splice_Rec_2154371,Human_Splice_Rec_2154407,Human_Splice_Rec_2154451,Human_Splice_Rec_2154493,Human_Splice_Rec_2154515,Human_Splice_Rec_2154533 RMVar_hsa_circ_48897,RMVar_hsa_circ_213764 90066 RMVar_ID_90066 Human_SNP_ID_701755961 m1A Human chr22 - 30906350 30906350 30906350 GGCCAGGCTGTGCAGGCGCCTGTATTTGTTGCAAGGGTGGCGCTCAGAAGATGTTGGGGCACATA GGCCAGGCTGTGCAGGCGCCTGTATTTGTTGCGAGGGTGGCGCTCAGAAGATGTTGGGGCACATA T C LOC107985544-001 RNACentral:URS0000BC4407 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30906173..30906359 26863196 MeRIP-seq:(Medium) rs1035189685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14454098 90067 RMVar_ID_90067 Human_SNP_ID_701763050 m1A Human chr22 - 30934877 30934877 30934877 GCCCCTCTGGTGCAGCAACTGTCACCATCTTTACTGCCCAACTCCAAGAGCCCTCGGGAGGTTCC GCCCCTCTGGTGCAGCAACTGTCACCATCTTTGCTGCCCAACTCCAAGAGCCCTCGGGAGGTTCC T C MORC2 Ensembl:ENSG00000133422 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:30934854..30934986 26863196 MeRIP-seq:(Medium) rs760570473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1028966,Human_RBP_ID_26822397,Human_RBP_ID_27035314 Human_Splice_Rec_2154593,Human_Splice_Rec_2154655 Human_miRNA_ID_2616470,Human_miRNA_ID_2885911 RMVar_hsa_circ_79916,RMVar_hsa_circ_82076,RMVar_hsa_circ_213767,RMVar_hsa_circ_213766,RMVar_hsa_circ_23829 90068 RMVar_ID_90068 Human_SNP_ID_701771440 m1A Human chr22 - 30968992 30968992 30968992 GTGGCCGGGGCTGTGTGCACTATCGGAGACAAAGCGGTGGCTGTGGTGTCTGTGACGGCGGCGGC GTGGCCGGGGCTGTGTGCACTATCGGAGACAAGGCGGTGGCTGTGGTGTCTGTGACGGCGGCGGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:30968909..30969054 26863196 MeRIP-seq:(Medium) rs1198434930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14455633 90069 RMVar_ID_90069 Human_SNP_ID_701771568 m1A Human chr22 + 30969299 30969299 30969299 GCGACGCAGCCGGGACGGTAGCTGCGGTGCGGACCGGAGGAGCCATCTTGTCTCGTCGCCGGGGA GCGACGCAGCCGGGACGGTAGCTGCGGTGCGGGCCGGAGGAGCCATCTTGTCTCGTCGCCGGGGA A G TUG1 Ensembl:ENSG00000253352 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30969251..30969850 26863196 MeRIP-seq:(Medium) rs967676573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1610127,Human_RBP_ID_4711329,Human_RBP_ID_5472977,Human_RBP_ID_7075003,Human_RBP_ID_14455637 Human_Splice_Rec_2154691,Human_Splice_Rec_2154693,Human_Splice_Rec_2154703,Human_Splice_Rec_2154707,Human_Splice_Rec_2154711 90070 RMVar_ID_90070 Human_SNP_ID_701799377 m1A Human chr22 - 31083245 31083245 31083245 CTAAGGCCTCGTCCGCCATCTCGCTGGCCCCTAGCTCCGTCGGTTCCTTTCTGGTGAGATCCCCA CTAAGGCCTCGTCCGCCATCTCGCTGGCCCCTTGCTCCGTCGGTTCCTTTCTGGTGAGATCCCCA T A AC005005.3 Ensembl:ENSG00000273387 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31083114..31083353 26863196 MeRIP-seq:(Medium) rs751437721 Functional Loss SNV dbSNP153 33..33 33 - - - 90071 RMVar_ID_90071 Human_SNP_ID_701800636 m1A Human chr22 + 31088063 31088063 31088063 CAGGAGCTGGAGCGCGAGGAGGAGGCCCTGGCATCCAAGCGTTTCCGTGCCGAGCGGCAGGACAA CAGGAGCTGGAGCGCGAGGAGGAGGCCCTGGCCTCCAAGCGTTTCCGTGCCGAGCGGCAGGACAA A C SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31087939..31088075 26863196 MeRIP-seq:(Medium) rs1194396566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962313,Human_RBP_ID_9392193,Human_RBP_ID_19008944,Human_RBP_ID_23015413 Human_Splice_Rec_2154780,Human_Splice_Rec_2154786,Human_Splice_Rec_2154792,Human_Splice_Rec_2154793,Human_Splice_Rec_2154799,Human_Splice_Rec_2154806,Human_Splice_Rec_2154807,Human_Splice_Rec_2154812,Human_Splice_Rec_2154813,Human_Splice_Rec_2154820,Human_Splice_Rec_2154824,Human_Splice_Rec_2154825,Human_Splice_Rec_2154864,Human_Splice_Rec_2154865,Human_Splice_Rec_2154902,Human_Splice_Rec_2154903,Human_Splice_Rec_2154942,Human_Splice_Rec_2154943,Human_Splice_Rec_2154980,Human_Splice_Rec_2154981,Human_Splice_Rec_2154990,Human_Splice_Rec_2154991,Human_Splice_Rec_2155028,Human_Splice_Rec_2155029,Human_Splice_Rec_2155068,Human_Splice_Rec_2155069,Human_Splice_Rec_2155077,Human_Splice_Rec_2155085 90072 RMVar_ID_90072 Human_SNP_ID_701800637 m1A Human chr22 + 31088063 31088063 31088063 CAGGAGCTGGAGCGCGAGGAGGAGGCCCTGGCATCCAAGCGTTTCCGTGCCGAGCGGCAGGACAA CAGGAGCTGGAGCGCGAGGAGGAGGCCCTGGCGTCCAAGCGTTTCCGTGCCGAGCGGCAGGACAA A G SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31087939..31088075 26863196 MeRIP-seq:(Medium) rs1194396566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962313,Human_RBP_ID_9392193,Human_RBP_ID_19008944,Human_RBP_ID_23015413 Human_Splice_Rec_2154780,Human_Splice_Rec_2154786,Human_Splice_Rec_2154792,Human_Splice_Rec_2154793,Human_Splice_Rec_2154799,Human_Splice_Rec_2154806,Human_Splice_Rec_2154807,Human_Splice_Rec_2154812,Human_Splice_Rec_2154813,Human_Splice_Rec_2154820,Human_Splice_Rec_2154824,Human_Splice_Rec_2154825,Human_Splice_Rec_2154864,Human_Splice_Rec_2154865,Human_Splice_Rec_2154902,Human_Splice_Rec_2154903,Human_Splice_Rec_2154942,Human_Splice_Rec_2154943,Human_Splice_Rec_2154980,Human_Splice_Rec_2154981,Human_Splice_Rec_2154990,Human_Splice_Rec_2154991,Human_Splice_Rec_2155028,Human_Splice_Rec_2155029,Human_Splice_Rec_2155068,Human_Splice_Rec_2155069,Human_Splice_Rec_2155077,Human_Splice_Rec_2155085 90073 RMVar_ID_90073 Human_SNP_ID_701801519 m1A Human chr22 + 31090873 31090873 31090873 TGTCGGTGCTCAGCCCCCGCCAACCAGCCCAGAACCGAGGTACTACCTATTCTCACCCTGCCTAG TGTCGGTGCTCAGCCCCCGCCAACCAGCCCAGGACCGAGGTACTACCTATTCTCACCCTGCCTAG A G SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr22:31090826..31091025;chr22:31090801..31091000 26863196 MeRIP-seq:(Medium) rs116823612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2154836,Human_Splice_Rec_2154837,Human_Splice_Rec_2154876,Human_Splice_Rec_2154877,Human_Splice_Rec_2154914,Human_Splice_Rec_2154915,Human_Splice_Rec_2154954,Human_Splice_Rec_2154955,Human_Splice_Rec_2155002,Human_Splice_Rec_2155003,Human_Splice_Rec_2155040,Human_Splice_Rec_2155041,Human_Splice_Rec_2155096,Human_Splice_Rec_2155097,Human_Splice_Rec_2155116,Human_Splice_Rec_2155117 RMVar_hsa_circ_126397,RMVar_hsa_circ_213778 90074 RMVar_ID_90074 Human_SNP_ID_701801601 m1A Human chr22 + 31091076 31091076 31091076 TCTCCTATGGCTGCTAGGCTCCAGGATGGCACACCCCAGGCTGCCCTAAGTCCCCTGACCCCCGC TCTCCTATGGCTGCTAGGCTCCAGGATGGCACGCCCCAGGCTGCCCTAAGTCCCCTGACCCCCGC A G SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31091028..31091146 26863196 MeRIP-seq:(Medium) rs765001494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152374,Human_RBP_ID_3963163,Human_RBP_ID_19008947 RMVar_hsa_circ_126397,RMVar_hsa_circ_213778 90075 RMVar_ID_90075 Human_SNP_ID_701803000 m1A Human chr22 + 31095451 31095451 31095451 GATGACTATTGAGGATGAAGGAGTCTTGGACAAGATGGTATAGCCAGATCCGGTGGGCTGGGGGT GATGACTATTGAGGATGAAGGAGTCTTGGACAGGATGGTATAGCCAGATCCGGTGGGCTGGGGGT A G SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31095420..31095521 26863196 MeRIP-seq:(Medium) rs1288665427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029005,Human_RBP_ID_3963167,Human_RBP_ID_27821620 Human_Splice_Rec_2154843,Human_Splice_Rec_2154883,Human_Splice_Rec_2154921,Human_Splice_Rec_2154961,Human_Splice_Rec_2155011,Human_Splice_Rec_2155047,Human_Splice_Rec_2155121,Human_Splice_Rec_2155131,Human_Splice_Rec_2155149 RMVar_hsa_circ_213779,RMVar_hsa_circ_126397,RMVar_hsa_circ_213778,RMVar_hsa_circ_334266 90076 RMVar_ID_90076 Human_SNP_ID_701803113 m1A Human chr22 + 31095814 31095812 31095814 TCCCTAGCTCCTTCTCTCCCGCTGGTGACCCCAGTTATTCTCCCCAACCAGCTTCTCTTCTCCTT TCCCTAGCTCCTTCTCTCCCGCTGGTGACCC__GTTATTCTCCCCAACCAGCTTCTCTTCTCCTT CCA C SMTN Ensembl:ENSG00000183963 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31095808..31095958 26863196 MeRIP-seq:(Medium) rs957389117 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17087452,Human_RBP_ID_18952501 RMVar_hsa_circ_213779,RMVar_hsa_circ_126397,RMVar_hsa_circ_213778,RMVar_hsa_circ_334266 90077 RMVar_ID_90077 Human_SNP_ID_701803367 m1A Human chr22 - 31096857 31096857 31096857 ACGAGCCGCTCAGTCTTGGTAACAGTGCTGACAGCAGAGCCATCAGCTGCCCGCTGGCTGTGCCT ACGAGCCGCTCAGTCTTGGTAACAGTGCTGACGGCAGAGCCATCAGCTGCCCGCTGGCTGTGCCT T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:31096807..31097008 32194978 MeRIP-seq:(Medium) rs781565083 Functional Loss SNV dbSNP153 33..33 33 - - - 90078 RMVar_ID_90078 Human_SNP_ID_701805471 m1A Human chr22 + 31104459 31104459 31104459 GCGACGCCACGAACTGCGCCTGCGCGGCAAGAATGTCTAGCCTGCCCGCCCGCATGGCCAGCCAG GCGACGCCACGAACTGCGCCTGCGCGGCAAGAGTGTCTAGCCTGCCCGCCCGCATGGCCAGCCAG A G SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31104409..31104493 26863196 MeRIP-seq:(Medium) rs1314530055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_393919,Human_miRNA_ID_399993,Human_miRNA_ID_405987,Human_miRNA_ID_411955 90079 RMVar_ID_90079 Human_SNP_ID_701805795 m1A Human chr22 - 31105204 31105204 31105204 TGCTGGGCCGCCGCTACGAGGAACTAGAGGTGAGGCCGTGGGAGGTGGGCTGGGGGCGAGGCCAG TGCTGGGCCGCCGCTACGAGGAACTAGAGGTGCGGCCGTGGGAGGTGGGCTGGGGGCGAGGCCAG T G SELENOM Ensembl:ENSG00000198832 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:31105201..31105225 32194978 MeRIP-seq:(Medium) rs1324982734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2155194,Human_Splice_Rec_2155200,Human_Splice_Rec_2155208,Human_Splice_Rec_2155216,Human_Splice_Rec_2155224,Human_Splice_Rec_2155232,Human_Splice_Rec_2155242,Human_Splice_Rec_2155250 RMVar_hsa_circ_87440,RMVar_hsa_circ_107343,RMVar_hsa_circ_96309,RMVar_hsa_circ_213782,RMVar_hsa_circ_213783,RMVar_hsa_circ_213781 90080 RMVar_ID_90080 Human_SNP_ID_701805957 m1A Human chr22 + 31105691 31105691 31105691 AGAATGGAATGTCCTGCGTGACGAAAGCCTTCACCTGGGGAGGAACCAGAGCATCAGAGACCATG AGAATGGAATGTCCTGCGTGACGAAAGCCTTCGCCTGGGGAGGAACCAGAGCATCAGAGACCATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:31105651..31105700 32194978 MeRIP-seq:(Medium) rs751271893 Functional Loss SNV dbSNP153 33..33 33 - - - 90081 RMVar_ID_90081 Human_SNP_ID_701811171 m1A Human chr22 + 31125471 31125471 31125471 TCAGCTAGAAAGAGGGATGCCCCAGCCCCTAGACCTCTCCCTGCTTCTGAGGGGCATCTCCAGCC TCAGCTAGAAAGAGGGATGCCCCAGCCCCTAGGCCTCTCCCTGCTTCTGAGGGGCATCTCCAGCC A G INPP5J Ensembl:ENSG00000185133 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31125420..31125576 26863196 MeRIP-seq:(Medium) rs1048684028 Functional Loss SNV dbSNP153 33..33 33 - - - 90082 RMVar_ID_90082 Human_SNP_ID_701811185 m1A Human chr22 - 31125510 31125510 31125510 CAGGGTGGGGAGCCTGTAGGACCAGATGTCTGAGCTGGAGGCTGGAGATGCCCCTCAGAAGCAGG CAGGGTGGGGAGCCTGTAGGACCAGATGTCTGGGCTGGAGGCTGGAGATGCCCCTCAGAAGCAGG T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31125272..31125617 26863196 MeRIP-seq:(Medium) rs1335479638 Functional Loss SNV dbSNP153 33..33 33 - - - 90083 RMVar_ID_90083 Human_SNP_ID_701811319 m1A Human chr22 + 31125800 31125800 31125800 GCCACCCCGATCACCCAGCCGTTCCCCAAGCCACTCCCCGAATCGCTCTCCCTGTGTTCCCCCAG GCCACCCCGATCACCCAGCCGTTCCCCAAGCCCCTCCCCGAATCGCTCTCCCTGTGTTCCCCCAG A C INPP5J Ensembl:ENSG00000185133 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31125705..31125887 26863196 MeRIP-seq:(Medium) rs1207573335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17088146 90084 RMVar_ID_90084 Human_SNP_ID_701811351 m1A Human chr22 + 31125852 31125852 31125852 TGTGTTCCCCCAGCCCCTGACATGGCCCTCCCAAGGCTTGGCACACAGAGTACAGGGCCTGGCAG TGTGTTCCCCCAGCCCCTGACATGGCCCTCCCGAGGCTTGGCACACAGAGTACAGGGCCTGGCAG A G INPP5J Ensembl:ENSG00000185133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31125803..31125921 26863196 MeRIP-seq:(Medium) rs1323491837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17088146 Human_Splice_Rec_2155360,Human_Splice_Rec_2155388 90085 RMVar_ID_90085 Human_SNP_ID_701815948 m1A Human chr22 + 31140308 31140308 31140308 ACCAGCGGAGGGCAGGGGAGCCCCCCAGGGCCACCCCCAGGAAGCCCAGCATCCCAAACAGCCCT ACCAGCGGAGGGCAGGGGAGCCCCCCAGGGCCGCCCCCAGGAAGCCCAGCATCCCAAACAGCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31140260..31140422 26863196 MeRIP-seq:(Medium) rs1319887624 Functional Loss SNV dbSNP153 33..33 33 - - - 90086 RMVar_ID_90086 Human_SNP_ID_701820651 m1A Human chr22 - 31160272 31160272 31160272 CCTGCCTCCGCACAGTTAACGCCAGCCCAGTCAATCAGTTTTTCGGGTACACGGCCAATACTAAC CCTGCCTCCGCACAGTTAACGCCAGCCCAGTCTATCAGTTTTTCGGGTACACGGCCAATACTAAC T A RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31160221..31160366 26863196 MeRIP-seq:(Medium) rs766645112 Functional Loss SNV dbSNP153 33..33 33 - - - 90087 RMVar_ID_90087 Human_SNP_ID_701820652 m1A Human chr22 + 31160274 31160274 31160274 TAGTATTGGCCGTGTACCCGAAAAACTGATTGACTGGGCTGGCGTTAACTGTGCGGAGGCAGGTA TAGTATTGGCCGTGTACCCGAAAAACTGATTGGCTGGGCTGGCGTTAACTGTGCGGAGGCAGGTA A G RNF185 Ensembl:ENSG00000138942 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31160223..31160351 26863196 MeRIP-seq:(Medium) rs1401311770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423632 Human_Splice_Rec_2155479,Human_Splice_Rec_2155491,Human_Splice_Rec_2155499,Human_Splice_Rec_2155509,Human_Splice_Rec_2155523,Human_Splice_Rec_2155533,Human_Splice_Rec_2155541 RMVar_hsa_circ_269284 90088 RMVar_ID_90088 Human_SNP_ID_701833715 m1A Human chr22 + 31212326 31212326 31212326 TGTGGTCTTCCCGCGCCTGAGGCGGCGGCGGCAGGAGCTGAGGGGAGTTGTAGGGAACTGAGGGG TGTGGTCTTCCCGCGCCTGAGGCGGCGGCGGCGGGAGCTGAGGGGAGTTGTAGGGAACTGAGGGG A G LIMK2 Ensembl:ENSG00000182541 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31212231..31212348 26863196 MeRIP-seq:(Medium) rs966965572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708571,Human_RBP_ID_18423633 Human_Splice_Rec_2155549,Human_Splice_Rec_2155553,Human_Splice_Rec_2155581 RMVar_hsa_circ_213789,RMVar_hsa_circ_94950 90089 RMVar_ID_90089 Human_SNP_ID_701847443 m1A Human chr22 - 31269832 31269832 31269832 ATTAGCCCCCTATGCAGGGCTCCATTCCCTGGACCCTCCGCATTCCACCCCAATGTACTAACCAT ATTAGCCCCCTATGCAGGGCTCCATTCCCTGGCCCCTCCGCATTCCACCCCAATGTACTAACCAT T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31269829..31270470 26863196 MeRIP-seq:(Medium) rs987002885 Functional Loss SNV dbSNP153 33..33 33 - - - 90090 RMVar_ID_90090 Human_SNP_ID_701849106 m1A Human chr22 + 31276511 31276511 31276511 GCAGGGGACAAAGGGCGGGCGGATCGGCGGGGAGGGGGCGGGGCGCGACCAGGCCAGGCCCGGGG GCAGGGGACAAAGGGCGGGCGGATCGGCGGGGGGGGGGCGGGGCGCGACCAGGCCAGGCCCGGGG A G LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31276509..31276591 26863410 MeRIP-seq:(Medium) rs987847101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676719,Human_RBP_ID_5120018,Human_RBP_ID_22725104,Human_RBP_ID_26789725 90091 RMVar_ID_90091 Human_SNP_ID_701866489 m1A Human chr22 - 31344971 31344968 31344971 TGGCATCGCCGGCAGCATGCAGCCAGAGGAGGAGGCAGCTCGGGCGGCTGGTGCAGCCATTGCAG TGGCATCGCCGGCAGCATGCAGCCAGAGGAGG___CAGCTCGGGCGGCTGGTGCAGCCATTGCAG GCCT G PATZ1 Ensembl:ENSG00000100105 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31344922..31345021 26863196 MeRIP-seq:(Medium) rs745974151 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_27306802 Human_miRNA_ID_2242628,Human_miRNA_ID_3011112 RMVar_hsa_circ_79834,RMVar_hsa_circ_213800 90092 RMVar_ID_90092 Human_SNP_ID_701866491 m1A Human chr22 - 31344971 31344971 31344971 TGGCATCGCCGGCAGCATGCAGCCAGAGGAGGAGGCAGCTCGGGCGGCTGGTGCAGCCATTGCAG TGGCATCGCCGGCAGCATGCAGCCAGAGGAGGGGGCAGCTCGGGCGGCTGGTGCAGCCATTGCAG T C PATZ1 Ensembl:ENSG00000100105 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31344922..31345021 26863196 MeRIP-seq:(Medium) rs201570433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27306802 Human_miRNA_ID_2242628,Human_miRNA_ID_3011112 RMVar_hsa_circ_79834,RMVar_hsa_circ_213800 90093 RMVar_ID_90093 Human_SNP_ID_701866492 m1A Human chr22 - 31344971 31344971 31344971 TGGCATCGCCGGCAGCATGCAGCCAGAGGAGGAGGCAGCTCGGGCGGCTGGTGCAGCCATTGCAG TGGCATCGCCGGCAGCATGCAGCCAGAGGAGGCGGCAGCTCGGGCGGCTGGTGCAGCCATTGCAG T G PATZ1 Ensembl:ENSG00000100105 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31344922..31345021 26863196 MeRIP-seq:(Medium) rs201570433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27306802 Human_miRNA_ID_2242628,Human_miRNA_ID_3011112 RMVar_hsa_circ_79834,RMVar_hsa_circ_213800 90094 RMVar_ID_90094 Human_SNP_ID_701866732 m1A Human chr22 + 31345637 31345637 31345637 CCGCCGCCCCCTCCCACTAGCCCGGCCGCTGCACCTGCCCGCCCCCTCCCTTCCCCTCAGCAGCG CCGCCGCCCCCTCCCACTAGCCCGGCCGCTGCCCCTGCCCGCCCCCTCCCTTCCCCTCAGCAGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31345282..31345932 26863196 MeRIP-seq:(Medium) rs1328962895 Functional Loss SNV dbSNP153 33..33 33 - - - 90095 RMVar_ID_90095 Human_SNP_ID_701866733 m1A Human chr22 + 31345637 31345637 31345637 CCGCCGCCCCCTCCCACTAGCCCGGCCGCTGCACCTGCCCGCCCCCTCCCTTCCCCTCAGCAGCG CCGCCGCCCCCTCCCACTAGCCCGGCCGCTGCTCCTGCCCGCCCCCTCCCTTCCCCTCAGCAGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31345282..31345932 26863196 MeRIP-seq:(Medium) rs1328962895 Functional Loss SNV dbSNP153 33..33 33 - - - 90096 RMVar_ID_90096 Human_SNP_ID_701867008 m1A Human chr22 + 31346293 31346282 31346293 CCCTTCCTCAGGCCGGGAGAAGGCGGCGGCGGAGCGGCGGCTGTGCGGCCCCGGGCTCCGTGTGT CCCTTCCTCAGGCCGGGAGAAG___________GCGGCGGCTGTGCGGCCCCGGGCTCCGTGTGT GGCGGCGGCGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:31346001..31346325 26863196 MeRIP-seq:(Medium) rs1314816440 Functional Loss DEL dbSNP153 23..33 33 - - - 90097 RMVar_ID_90097 Human_SNP_ID_701880927 m1A Human chr22 + 31399667 31399667 31399667 GCGGGTGTGTGAAGGGAGACAGTGTGGAGGCCACAGGGTACTCGCCACGATGAGCAGCACCTTAG GCGGGTGTGTGAAGGGAGACAGTGTGGAGGCCGCAGGGTACTCGCCACGATGAGCAGCACCTTAG A G DRG1 Ensembl:ENSG00000185721 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:31399601..31399773;chr22:31399601..31399772;chr22:31399601..31399769 26863196 MeRIP-seq:(Medium) rs957141612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781703,Human_RBP_ID_1610302,Human_RBP_ID_4693152,Human_RBP_ID_5324165,Human_RBP_ID_7075565,Human_RBP_ID_9348372,Human_RBP_ID_22455202,Human_RBP_ID_23212732,Human_RBP_ID_27841112 Human_Splice_Rec_2155761,Human_Splice_Rec_2155777,Human_Splice_Rec_2155787,Human_Splice_Rec_2155799 RMVar_hsa_circ_113269,RMVar_hsa_circ_122524,RMVar_hsa_circ_213801,RMVar_hsa_circ_213802 90098 RMVar_ID_90098 Human_SNP_ID_701881209 m1A Human chr22 + 31400605 31400605 31400605 GAAGCGTTCACTGCTTCTAATTTATGGCTGTGATTCCTCCCTTTTAGATGGCTCGGACTCAAAAG GAAGCGTTCACTGCTTCTAATTTATGGCTGTGGTTCCTCCCTTTTAGATGGCTCGGACTCAAAAG A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31400601..31400750 26863196 MeRIP-seq:(Medium) rs765563870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14458260 RMVar_hsa_circ_113269,RMVar_hsa_circ_122524,RMVar_hsa_circ_213801,RMVar_hsa_circ_213802 90099 RMVar_ID_90099 Human_SNP_ID_701881210 m1A Human chr22 + 31400605 31400605 31400605 GAAGCGTTCACTGCTTCTAATTTATGGCTGTGATTCCTCCCTTTTAGATGGCTCGGACTCAAAAG GAAGCGTTCACTGCTTCTAATTTATGGCTGTGTTTCCTCCCTTTTAGATGGCTCGGACTCAAAAG A T DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31400601..31400750 26863196 MeRIP-seq:(Medium) rs765563870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14458260 RMVar_hsa_circ_113269,RMVar_hsa_circ_122524,RMVar_hsa_circ_213801,RMVar_hsa_circ_213802 90100 RMVar_ID_90100 Human_SNP_ID_701881226 m1A Human chr22 + 31400661 31400661 31400661 ACTCAAAAGAACAAGGCCACAGCACACCACTTAGGGCTGCTTAAGGCTCGTCTTGCTAAGCTTCG ACTCAAAAGAACAAGGCCACAGCACACCACTTGGGGCTGCTTAAGGCTCGTCTTGCTAAGCTTCG A G DRG1 Ensembl:ENSG00000185721 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:31399720..31420376 32194978 MeRIP-seq:(Medium) rs1223391338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_578428,Human_RBP_ID_14458262,Human_RBP_ID_18787500,Human_RBP_ID_26823064 Human_Splice_Rec_2155762,Human_Splice_Rec_2155763,Human_Splice_Rec_2155778,Human_Splice_Rec_2155779,Human_Splice_Rec_2155788,Human_Splice_Rec_2155789 RMVar_hsa_circ_34603,RMVar_hsa_circ_113269,RMVar_hsa_circ_122524,RMVar_hsa_circ_213801,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_213803 90101 RMVar_ID_90101 Human_SNP_ID_701890575 m1A Human chr22 - 31435423 31435423 31435423 ATATTGTTACCCACCACACCAAGATTTTCATCAACCAGTTTCACATAATCAGAGCAATCCCCTTA ATATTGTTACCCACCACACCAAGATTTTCATCCACCAGTTTCACATAATCAGAGCAATCCCCTTA T G lnc-EIF4ENIF1-2,lnc-EIF4ENIF1-3,RF00017-1003 RNACentral:URS00008B6A8D,RNACentral:URS00008B6D28,RNACentral:URS0000945854 lincRNA,lincRNA,SRP RNA exon,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31435377..31435463 26863196 MeRIP-seq:(Medium) rs1297210924 Functional Loss SNV dbSNP153 33..33 33 - - - 90102 RMVar_ID_90102 Human_SNP_ID_701893124 m1A Human chr22 + 31444254 31444254 31444254 TGAACTCCCCTGCAAGTTTCAATAGACTCCCCACTGTCTGACCCAGTCACCTCTGTCCACTTCAC TGAACTCCCCTGCAAGTTTCAATAGACTCCCCGCTGTCTGACCCAGTCACCTCTGTCCACTTCAC A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31444249..31444353 26863196 MeRIP-seq:(Medium) rs1403799392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14459122 90103 RMVar_ID_90103 Human_SNP_ID_701897202 m1A Human chr22 + 31458602 31458602 31458602 CCTGATCAGCCGCAGGCTCCTGTGCAAGGATGACCTCCACTTCATCCTCTTCGGCCACTCCTCCA CCTGATCAGCCGCAGGCTCCTGTGCAAGGATGGCCTCCACTTCATCCTCTTCGGCCACTCCTCCA A G AL096701.3,DRG1 Ensembl:ENSG00000240591,Ensembl:ENSG00000185721 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31458555..31458697 26863196 MeRIP-seq:(Medium) rs1406601643 Functional Loss SNV dbSNP153 33..33 33 - - - 90104 RMVar_ID_90104 Human_SNP_ID_701898575 m1A Human chr22 + 31463784 31463784 31463784 GACGGTGATCCTTCTCAAAGGTCCGGGCAGAGATTATCCTCCCACTGCCAATCCTACGTCCACCA GACGGTGATCCTTCTCAAAGGTCCGGGCAGAGGTTATCCTCCCACTGCCAATCCTACGTCCACCA A G AL096701.3,DRG1 Ensembl:ENSG00000240591,Ensembl:ENSG00000185721 lincRNA,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31463733..31463987 26863196 MeRIP-seq:(Medium) rs1390425570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5600714 Human_Splice_Rec_2156022,Human_Splice_Rec_2156024,Human_Splice_Rec_2156026 90105 RMVar_ID_90105 Human_SNP_ID_701905547 m1A Human chr22 + 31488744 31488744 31488744 TATCCATGGCTCCTTGGTCTACAATGCTCTGCACCTGGAAGATAAATCGGCACAAAATTGTCACC TATCCATGGCTCCTTGGTCTACAATGCTCTGCCCCTGGAAGATAAATCGGCACAAAATTGTCACC A C SFI1,DRG1 Ensembl:ENSG00000198089,Ensembl:ENSG00000185721 Protein coding,Protein coding exon,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:31488725..31488838 26863196 MeRIP-seq:(Medium) rs1431129000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2156027 90106 RMVar_ID_90106 Human_SNP_ID_701905548 m1A Human chr22 - 31488747 31488747 31488747 CTCGGTGACAATTTTGTGCCGATTTATCTTCCAGGTGCAGAGCATTGTAGACCAAGGAGCCATGG CTCGGTGACAATTTTGTGCCGATTTATCTTCCGGGTGCAGAGCATTGTAGACCAAGGAGCCATGG T C EIF4ENIF1 Ensembl:ENSG00000184708 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:31488626..31489211;chr22:31471853..31489211;chr22:31488558..31488814 26863196 MeRIP-seq:(Medium) rs916114261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423728,Human_RBP_ID_19008975 90107 RMVar_ID_90107 Human_SNP_ID_701907974 m1A Human chr22 + 31496587 31496587 31496587 CGGGAGTTAAGAAGCAGGTCCCGGATCGCCGTATACCGCCGGGTTTTCTCCCAACGTCAGGCCCG CGGGAGTTAAGAAGCAGGTCCCGGATCGCCGTGTACCGCCGGGTTTTCTCCCAACGTCAGGCCCG A G SFI1,DRG1 Ensembl:ENSG00000198089,Ensembl:ENSG00000185721 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31496452..31496628 26863196 MeRIP-seq:(Medium) rs542385791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708573 Human_Splice_Rec_2156031,Human_Splice_Rec_2156091,Human_Splice_Rec_2156153,Human_Splice_Rec_2156209,Human_Splice_Rec_2156215,Human_Splice_Rec_2156223,Human_Splice_Rec_2156287,Human_Splice_Rec_2156347,Human_Splice_Rec_2156353 90108 RMVar_ID_90108 Human_SNP_ID_701925104 m1A Human chr22 + 31561320 31561320 31561320 AGGGTGTGGTGGAGCACGTGGAGGCAGCGACTAGGACAGGTCCGTGTGAGCCGTGCCCTCCATGC AGGGTGTGGTGGAGCACGTGGAGGCAGCGACTGGGACAGGTCCGTGTGAGCCGTGCCCTCCATGC A G SFI1 Ensembl:ENSG00000198089 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:31561309..31561396 26863410 MeRIP-seq:(Medium) rs777428105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2156042,Human_Splice_Rec_2156043,Human_Splice_Rec_2156104,Human_Splice_Rec_2156105,Human_Splice_Rec_2156158,Human_Splice_Rec_2156159,Human_Splice_Rec_2156236,Human_Splice_Rec_2156237,Human_Splice_Rec_2156296,Human_Splice_Rec_2156297,Human_Splice_Rec_2156366,Human_Splice_Rec_2156367,Human_Splice_Rec_2156424,Human_Splice_Rec_2156425,Human_Splice_Rec_2156456 RMVar_hsa_circ_6488,RMVar_hsa_circ_43878,RMVar_hsa_circ_297414,RMVar_hsa_circ_36395,RMVar_hsa_circ_32706,RMVar_hsa_circ_81990,RMVar_hsa_circ_213839,RMVar_hsa_circ_332016,RMVar_hsa_circ_345659,RMVar_hsa_circ_266413,RMVar_hsa_circ_47576,RMVar_hsa_circ_291470,RMVar_hsa_circ_213840,RMVar_hsa_circ_288910,RMVar_hsa_circ_43167,RMVar_hsa_circ_213842,RMVar_hsa_circ_27357,RMVar_hsa_circ_27988,RMVar_hsa_circ_12484,RMVar_hsa_circ_213843,RMVar_hsa_circ_345147,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976 90109 RMVar_ID_90109 Human_SNP_ID_701927969 m1A Human chr22 + 31572030 31572030 31572030 GCCAAGGCAGTAAACTCGGGAAGGTGAGAGATAGCCAGAGCTGGACAGGGTTGGGAGGGGACTGA GCCAAGGCAGTAAACTCGGGAAGGTGAGAGATGGCCAGAGCTGGACAGGGTTGGGAGGGGACTGA A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31572027..31572124 26863196 MeRIP-seq:(Medium) rs1467168241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6488,RMVar_hsa_circ_43878,RMVar_hsa_circ_36395,RMVar_hsa_circ_32706,RMVar_hsa_circ_81990,RMVar_hsa_circ_345659,RMVar_hsa_circ_266413,RMVar_hsa_circ_47576,RMVar_hsa_circ_213840,RMVar_hsa_circ_288910,RMVar_hsa_circ_43167,RMVar_hsa_circ_213842,RMVar_hsa_circ_27357,RMVar_hsa_circ_27988,RMVar_hsa_circ_12484,RMVar_hsa_circ_213843,RMVar_hsa_circ_345147,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976 90110 RMVar_ID_90110 Human_SNP_ID_701928182 m1A Human chr22 - 31572991 31572991 31572991 AGGCAGGAAAACAGGGTGAAGTACAGGTGGAGAGGGAAAAGAGAAAGGCACACACGCTGGAAAGG AGGCAGGAAAACAGGGTGAAGTACAGGTGGAGGGGGAAAAGAGAAAGGCACACACGCTGGAAAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31572990..31573093 26863196 MeRIP-seq:(Medium) rs1253352300 Functional Loss SNV dbSNP153 33..33 33 - - - 90111 RMVar_ID_90111 Human_SNP_ID_701939895 m1A Human chr22 - 31611864 31611864 31611864 TCACAGGCCAGAGGATGGAGAAGGAAGTGCAGAGGGGACATCTCCTGGGTTCCCACCTGTTGTCT TCACAGGCCAGAGGATGGAGAAGGAAGTGCAGTGGGGACATCTCCTGGGTTCCCACCTGTTGTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31611857..31611955 26863196 MeRIP-seq:(Medium) rs536040116 Functional Loss SNV dbSNP153 33..33 33 - - - 90112 RMVar_ID_90112 Human_SNP_ID_701943450 m1A Human chr22 + 31621073 31621073 31621073 GGAAGCAGTGGTAGTCCCCAGGGGCCAGGTAGATGACACAGTGATAGAGCTCATTCCCTTCCCGG GGAAGCAGTGGTAGTCCCCAGGGGCCAGGTAGGTGACACAGTGATAGAGCTCATTCCCTTCCCGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:31621023..31621222 32194978 MeRIP-seq:(Medium) rs1246822228 Functional Loss SNV dbSNP153 33..33 33 - - - 90113 RMVar_ID_90113 Human_SNP_ID_701944666 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GG________________________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 3..34 33 - - - 90114 RMVar_ID_90114 Human_SNP_ID_701944667 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACAC____________________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 7..34 33 - - - 90115 RMVar_ID_90115 Human_SNP_ID_701944668 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACAC__________________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 9..34 33 - - - 90116 RMVar_ID_90116 Human_SNP_ID_701944669 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACAC________________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 11..34 33 - - - 90117 RMVar_ID_90117 Human_SNP_ID_701944670 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACAC______________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 13..34 33 - - - 90118 RMVar_ID_90118 Human_SNP_ID_701944671 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACAC____________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 15..34 33 - - - 90119 RMVar_ID_90119 Human_SNP_ID_701944672 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACAC__________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 17..34 33 - - - 90120 RMVar_ID_90120 Human_SNP_ID_701944673 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACAC________________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 19..34 33 - - - 90121 RMVar_ID_90121 Human_SNP_ID_701944674 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACAC______________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 21..34 33 - - - 90122 RMVar_ID_90122 Human_SNP_ID_701944675 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACAC____________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 23..34 33 - - - 90123 RMVar_ID_90123 Human_SNP_ID_701944676 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACACAC__________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 25..34 33 - - - 90124 RMVar_ID_90124 Human_SNP_ID_701944677 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACACACAC________ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 27..34 33 - - - 90125 RMVar_ID_90125 Human_SNP_ID_701944678 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACACACACAC______ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 29..34 33 - - - 90126 RMVar_ID_90126 Human_SNP_ID_701944679 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACACACACACAC____ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 31..34 33 - - - 90127 RMVar_ID_90127 Human_SNP_ID_701944680 m1A Human chr22 + 31624743 31624712 31624744 GGACACACACACACACACACACACACACACACACACACACACACACGAGACCCAAGCCCCTCCTT GGACACACACACACACACACACACACACACAC__ACACACACACACGAGACCCAAGCCCCTCCTT GACACACACACACACACACACACACACACACAC GACACACACACACACACACACACACACACAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31624741..31624806 26863196 MeRIP-seq:(Medium) rs55946723 Functional Loss DEL dbSNP153 33..34 33 - - - 90128 RMVar_ID_90128 Human_SNP_ID_701945988 m1A Human chr22 + 31629273 31629270 31629273 AGGTGCATGTAGGTGGAAGTGTGTGTGCATGGAGGATACGTGTGCAGGTGCAAGGGTATGTGCAT AGGTGCATGTAGGTGGAAGTGTGTGTGCAT___GGATACGTGTGCAGGTGCAAGGGTATGTGCAT TGGA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31629253..31629385 26863196 MeRIP-seq:(Medium) rs1231213590 Functional Loss DEL dbSNP153 31..33 33 - - - 90129 RMVar_ID_90129 Human_SNP_ID_701980374 m1A Human chr22 + 31754102 31754102 31754102 GCGTAGGCGGGGTATCTGGAGGAGGCGCAGGGAACCTGGAGAGGGTCCAGCCCTCAGTGCCCCGG GCGTAGGCGGGGTATCTGGAGGAGGCGCAGGGCACCTGGAGAGGGTCCAGCCCTCAGTGCCCCGG A C DEPDC5 Ensembl:ENSG00000100150 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:31753915..31754143 26863196 MeRIP-seq:(Medium) rs991508803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423638 Human_Splice_Rec_2158109,Human_Splice_Rec_2158189,Human_Splice_Rec_2158271,Human_Splice_Rec_2158353,Human_Splice_Rec_2158435,Human_Splice_Rec_2158477,Human_Splice_Rec_2158561,Human_Splice_Rec_2158577,Human_Splice_Rec_2158657,Human_Splice_Rec_2158699,Human_Splice_Rec_2158781,Human_Splice_Rec_2158829,Human_Splice_Rec_2158909,Human_Splice_Rec_2158985 90130 RMVar_ID_90130 Human_SNP_ID_701980375 m1A Human chr22 + 31754103 31754103 31754103 CGTAGGCGGGGTATCTGGAGGAGGCGCAGGGAACCTGGAGAGGGTCCAGCCCTCAGTGCCCCGGC CGTAGGCGGGGTATCTGGAGGAGGCGCAGGGAGCCTGGAGAGGGTCCAGCCCTCAGTGCCCCGGC A G DEPDC5 Ensembl:ENSG00000100150 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31754009..31754155 26863196 MeRIP-seq:(Medium) rs1416339547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423638 Human_Splice_Rec_2158109,Human_Splice_Rec_2158189,Human_Splice_Rec_2158271,Human_Splice_Rec_2158353,Human_Splice_Rec_2158435,Human_Splice_Rec_2158477,Human_Splice_Rec_2158561,Human_Splice_Rec_2158577,Human_Splice_Rec_2158657,Human_Splice_Rec_2158699,Human_Splice_Rec_2158781,Human_Splice_Rec_2158829,Human_Splice_Rec_2158909,Human_Splice_Rec_2158985 90131 RMVar_ID_90131 Human_SNP_ID_701980592 m1A Human chr22 + 31754888 31754888 31754888 TGGCAGGGAGGCAAGATGACTTCTCTGCCCCAAGCTTGGAACAGCTAAAGGGAAAAACAGTGCAA TGGCAGGGAGGCAAGATGACTTCTCTGCCCCACGCTTGGAACAGCTAAAGGGAAAAACAGTGCAA A C DEPDC5 Ensembl:ENSG00000100150 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31753914..31754964 26863196 MeRIP-seq:(Medium) rs765660840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2156832,Human_Splice_Rec_2156833,Human_Splice_Rec_2156910,Human_Splice_Rec_2156911,Human_Splice_Rec_2156956,Human_Splice_Rec_2156957,Human_Splice_Rec_2157006,Human_Splice_Rec_2157007,Human_Splice_Rec_2157090,Human_Splice_Rec_2157091,Human_Splice_Rec_2157172,Human_Splice_Rec_2157173,Human_Splice_Rec_2157252,Human_Splice_Rec_2157253,Human_Splice_Rec_2157268,Human_Splice_Rec_2157269,Human_Splice_Rec_2157280,Human_Splice_Rec_2157281,Human_Splice_Rec_2157360,Human_Splice_Rec_2157361,Human_Splice_Rec_2157442,Human_Splice_Rec_2157443,Human_Splice_Rec_2157522,Human_Splice_Rec_2157523,Human_Splice_Rec_2157564,Human_Splice_Rec_2157565,Human_Splice_Rec_2157644,Human_Splice_Rec_2157646,Human_Splice_Rec_2157647,Human_Splice_Rec_2157730,Human_Splice_Rec_2157731,Human_Splice_Rec_2157770,Human_Splice_Rec_2157771,Human_Splice_Rec_2157852,Human_Splice_Rec_2157853,Human_Splice_Rec_2157934,Human_Splice_Rec_2157935,Human_Splice_Rec_2158018,Human_Splice_Rec_2158019,Human_Splice_Rec_2158032,Human_Splice_Rec_2158033,Human_Splice_Rec_2158110,Human_Splice_Rec_2158111,Human_Splice_Rec_2158190,Human_Splice_Rec_2158191,Human_Splice_Rec_2158272,Human_Splice_Rec_2158273,Human_Splice_Rec_2158354,Human_Splice_Rec_2158355,Human_Splice_Rec_2158436,Human_Splice_Rec_2158437,Human_Splice_Rec_2158478,Human_Splice_Rec_2158479,Human_Splice_Rec_2158562,Human_Splice_Rec_2158563,Human_Splice_Rec_2158578,Human_Splice_Rec_2158579,Human_Splice_Rec_2158658,Human_Splice_Rec_2158659,Human_Splice_Rec_2158700,Human_Splice_Rec_2158701,Human_Splice_Rec_2158782,Human_Splice_Rec_2158783,Human_Splice_Rec_2158830,Human_Splice_Rec_2158831,Human_Splice_Rec_2158910,Human_Splice_Rec_2158911,Human_Splice_Rec_2158986,Human_Splice_Rec_2158987,Human_Splice_Rec_2159067,Human_Splice_Rec_2159105,Human_Splice_Rec_2159185,Human_Splice_Rec_2159691 RMVar_hsa_circ_18781,RMVar_hsa_circ_47860 90132 RMVar_ID_90132 Human_SNP_ID_702029533 m1A Human chr22 + 31944586 31944579 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGCT_______GCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG TGCCTGCA T YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) rs71697452 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 90133 RMVar_ID_90133 Human_SNP_ID_702029539 m1A Human chr22 + 31944586 31944585 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGC_GCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG CA C YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) rs1177688436 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 90134 RMVar_ID_90134 Human_SNP_ID_702029540 m1A Human chr22 + 31944586 31944586 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCCGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG A C YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) rs1043051300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 90135 RMVar_ID_90135 Human_SNP_ID_702029541 m1A Human chr22 + 31944586 31944586 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCGGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG A G YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) rs1043051300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 90136 RMVar_ID_90136 Human_SNP_ID_702029542 m1A Human chr22 + 31944586 31944586 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCTGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG A T YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) rs1043051300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 90137 RMVar_ID_90137 Human_SNP_ID_702029553 m1A Human chr22 + 31944600 31944600 31944600 AGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCGAGCCAGTGCGCGTG AGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCGGCCTCCGGCCGGCCGGCGAGCCAGTGCGCGTG A G YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:31944552..31944684 26863196 MeRIP-seq:(Medium) rs865907627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4693756,Human_RBP_ID_5240830,Human_RBP_ID_5324763,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639,Human_RBP_ID_23943926,Human_RBP_ID_26770975 Human_miRNA_ID_2716761,Human_miRNA_ID_3052743 90138 RMVar_ID_90138 Human_SNP_ID_702029576 m1A Human chr22 - 31944646 31944646 31944646 CCGCCGGTCAGTCCGCTCCCCGGTCGCTGCGGAGGCCGCCGCCGCGCACGCGCACTGGCTCGCCG CCGCCGGTCAGTCCGCTCCCCGGTCGCTGCGGCGGCCGCCGCCGCGCACGCGCACTGGCTCGCCG T G C22orf24 Ensembl:ENSG00000128254 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:31944526..31944804 26863196 MeRIP-seq:(Medium) rs1486222692 Functional Loss SNV dbSNP153 33..33 33 - - - 90139 RMVar_ID_90139 Human_SNP_ID_702029598 m1A Human chr22 + 31944694 31944693 31944694 AGCGGACTGACCGGCGGGAGGGCTAGCGAGCCAGCGGTGTGAGGCGCGAGGCGAGGCCGAGCCGC AGCGGACTGACCGGCGGGAGGGCTAGCGAGCC_GCGGTGTGAGGCGCGAGGCGAGGCCGAGCCGC CA C YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr22:31944501..31944849;chr22:31944501..31944825 26863196 MeRIP-seq:(Medium) rs755526658 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4708152,Human_RBP_ID_5324764,Human_RBP_ID_8943160,Human_RBP_ID_9300345,Human_RBP_ID_9332799,Human_RBP_ID_22454611,Human_RBP_ID_26770975,Human_RBP_ID_27035943 Human_miRNA_ID_2084623,Human_miRNA_ID_2451229 90140 RMVar_ID_90140 Human_SNP_ID_702032931 m1A Human chr22 + 31956774 31956774 31956774 ACCCTCTGGACGAGCGACCAGCAGGATGAAGAAGCAGGAGAAGGCAACTGAAGATCCTTCAGGTC ACCCTCTGGACGAGCGACCAGCAGGATGAAGAGGCAGGAGAAGGCAACTGAAGATCCTTCAGGTC A G YWHAH Ensembl:ENSG00000128245 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:31956474..31956916 32194978 MeRIP-seq:(Medium) rs139643031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_578580,Human_RBP_ID_7076604,Human_RBP_ID_14462967,Human_RBP_ID_20750661,Human_RBP_ID_27307027,Human_RBP_ID_27493362 RMVar_hsa_circ_126928,RMVar_hsa_circ_213919 90141 RMVar_ID_90141 Human_SNP_ID_702052565 m1A Human chr22 + 32039773 32039773 32039773 GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATGATTGAAGTAGATCCTGACACTAAGGAAATGCT A G Z74021.1 Ensembl:ENSG00000232346 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs373723834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5275956,Human_RBP_ID_26501422 90142 RMVar_ID_90142 Human_SNP_ID_702052566 m1A Human chr22 + 32039773 32039773 32039773 GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATTATTGAAGTAGATCCTGACACTAAGGAAATGCT A T Z74021.1 Ensembl:ENSG00000232346 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs373723834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5275956,Human_RBP_ID_26501422 90143 RMVar_ID_90143 Human_SNP_ID_702148278 m1A Human chr22 - 32398051 32398051 32398051 AGGCAACCATTATGCAGAAATCCAGGTTGTGGATGAGATTTTCAATGAGTATGCTGCTAAAAAAA AGGCAACCATTATGCAGAAATCCAGGTTGTGGGTGAGATTTTCAATGAGTATGCTGCTAAAAAAA T C RTCB Ensembl:ENSG00000100220 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr22:32398026..32398050;chr22:32397926..32398125 26863196,32194978 MeRIP-seq:(Medium) rs1569441439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1942056,Human_RBP_ID_8548924,Human_RBP_ID_17985109,Human_RBP_ID_23944086 Human_Splice_Rec_2160068,Human_Splice_Rec_2160080,Human_Splice_Rec_2160088,Human_Splice_Rec_2160096 Human_miRNA_ID_2231639,Human_miRNA_ID_3042056 RMVar_hsa_circ_79972,RMVar_hsa_circ_112298,RMVar_hsa_circ_96948,RMVar_hsa_circ_213924,RMVar_hsa_circ_213925,RMVar_hsa_circ_213923,RMVar_hsa_circ_127521,RMVar_hsa_circ_213930,RMVar_hsa_circ_213931 90144 RMVar_ID_90144 Human_SNP_ID_702148292 m1A Human chr22 + 32398100 32398100 32398100 TGCATAATGGTTGCCTGCTCCCAGGGTCCCCAACTGCAAATGTAAAAATGTCTGGTAAGATAGTT TGCATAATGGTTGCCTGCTCCCAGGGTCCCCAGCTGCAAATGTAAAAATGTCTGGTAAGATAGTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:32397926..32398162 26863196 MeRIP-seq:(Medium) rs750059803 Functional Loss SNV dbSNP153 33..33 33 - - - 90145 RMVar_ID_90145 Human_SNP_ID_702148723 m1A Human chr22 + 32399696 32399695 32399696 CTTCCGTACTCCTCGCAGTGCTCCTTGTCTTCAGCCCAGGCATACCCTTCTCTTAAGGACCAGTC CTTCCGTACTCCTCGCAGTGCTCCTTGTCTTC_GCCCAGGCATACCCTTCTCTTAAGGACCAGTC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:32399556..32399798;chr22:32399601..32399800;chr22:32399549..32399750 26863196 MeRIP-seq:(Medium) rs1222780649 Functional Loss DEL dbSNP153 33..33 33 - - - 90146 RMVar_ID_90146 Human_SNP_ID_702148731 m1A Human chr22 - 32399717 32399717 32399717 GAGGCCTTGGAGATGGGGGTGGACTGGTCCTTAAGAGAAGGGTATGCCTGGGCTGAAGACAAGGA GAGGCCTTGGAGATGGGGGTGGACTGGTCCTTGAGAGAAGGGTATGCCTGGGCTGAAGACAAGGA T C RTCB Ensembl:ENSG00000100220 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:32399601..32399750 32194978 MeRIP-seq:(Medium) rs745957294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245862,Human_RBP_ID_833995,Human_RBP_ID_4711562,Human_RBP_ID_7076731,Human_RBP_ID_9392210,Human_RBP_ID_14463455,Human_RBP_ID_22507907,Human_RBP_ID_22550693,Human_RBP_ID_22675693,Human_RBP_ID_23944090 Human_Splice_Rec_2160066,Human_Splice_Rec_2160086,Human_Splice_Rec_2160094 Human_miRNA_ID_3119305 RMVar_hsa_circ_79972,RMVar_hsa_circ_96948,RMVar_hsa_circ_213924,RMVar_hsa_circ_213923,RMVar_hsa_circ_127521,RMVar_hsa_circ_213930,RMVar_hsa_circ_213931 90147 RMVar_ID_90147 Human_SNP_ID_702169328 m1A Human chr22 - 32475345 32475345 32475345 CGGGAGGCCGGGCCATGTTCTCCAGGAGCCGGACCCCAGCCGACCACCCGCGCTTCCCGTCGCCT CGGGAGGCCGGGCCATGTTCTCCAGGAGCCGGTCCCCAGCCGACCACCCGCGCTTCCCGTCGCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:32475217..32475401 26863196 MeRIP-seq:(Medium) rs780528326 Functional Loss SNV dbSNP153 33..33 33 - - - 90148 RMVar_ID_90148 Human_SNP_ID_702249501 m1A Human chr22 + 32801992 32801980 32801992 GAGAGGCGAGCAGCAGCCCCGGCAGCGGCGGCAGCAGCGGCAATGACCCCTTGGCTCGGGCTCAT GAGAGGCGAGCAGCAGCCCCG____________GCAGCGGCAATGACCCCTTGGCTCGGGCTCAT GGCAGCGGCGGCA G TIMP3 Ensembl:ENSG00000100234 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr22:32801701..32802139;chr22:32801701..32802000 26863196 MeRIP-seq:(Medium) rs1261092127 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_833315,Human_RBP_ID_4708157,Human_RBP_ID_5529918,Human_RBP_ID_18471470,Human_RBP_ID_22454615 Human_miRNA_ID_2939191 90149 RMVar_ID_90149 Human_SNP_ID_702249513 m1A Human chr22 + 32801992 32801992 32801992 GAGAGGCGAGCAGCAGCCCCGGCAGCGGCGGCAGCAGCGGCAATGACCCCTTGGCTCGGGCTCAT GAGAGGCGAGCAGCAGCCCCGGCAGCGGCGGCGGCAGCGGCAATGACCCCTTGGCTCGGGCTCAT A G TIMP3 Ensembl:ENSG00000100234 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr22:32801701..32802139;chr22:32801701..32802000 26863196 MeRIP-seq:(Medium) rs1205570462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833315,Human_RBP_ID_4708157,Human_RBP_ID_5529918,Human_RBP_ID_18471470,Human_RBP_ID_22454615 Human_miRNA_ID_2939191 90150 RMVar_ID_90150 Human_SNP_ID_702249517 m1A Human chr22 + 32802001 32802001 32802001 GCAGCAGCCCCGGCAGCGGCGGCAGCAGCGGCAATGACCCCTTGGCTCGGGCTCATCGTGCTCCT GCAGCAGCCCCGGCAGCGGCGGCAGCAGCGGCGATGACCCCTTGGCTCGGGCTCATCGTGCTCCT A G TIMP3 Ensembl:ENSG00000100234 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:32801787..32802025 26863196 MeRIP-seq:(Medium) rs758200076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833315,Human_RBP_ID_4708157,Human_RBP_ID_5529918,Human_RBP_ID_18471470,Human_RBP_ID_22454615 Human_miRNA_ID_2937816,Human_miRNA_ID_2939191 90151 RMVar_ID_90151 Human_SNP_ID_702249832 m1A Human chr22 + 32803311 32803311 32803311 AATTTTCCACTGAGTCTTGGGTGAGGGACTCTACCAGCGTGTTGTGGTGAGGAGGGGGAGGAGGT AATTTTCCACTGAGTCTTGGGTGAGGGACTCTGCCAGCGTGTTGTGGTGAGGAGGGGGAGGAGGT A G TIMP3 Ensembl:ENSG00000100234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:32803308..32803399 26863196 MeRIP-seq:(Medium) rs940813032 Functional Loss SNV dbSNP153 33..33 33 - - - 90152 RMVar_ID_90152 Human_SNP_ID_702252329 m1A Human chr22 + 32814177 32814176 32814178 AGAGAGAGAGAGAGAGAGAGAGAAAGAGAAAGAAAGAAAAGAAAGAAAGAAAGAAAGAAAGAAAA AGAGAGAGAGAGAGAGAGAGAGAAAGAGAAAG__AGAAAAGAAAGAAAGAAAGAAAGAAAGAAAA GAA G TIMP3 Ensembl:ENSG00000100234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:32814174..32814415 26863196 MeRIP-seq:(Medium) rs1389250675 Functional Loss DEL dbSNP153 33..34 33 - - - 90153 RMVar_ID_90153 Human_SNP_ID_702252330 m1A Human chr22 + 32814177 32814177 32814177 AGAGAGAGAGAGAGAGAGAGAGAAAGAGAAAGAAAGAAAAGAAAGAAAGAAAGAAAGAAAGAAAA AGAGAGAGAGAGAGAGAGAGAGAAAGAGAAAGTAAGAAAAGAAAGAAAGAAAGAAAGAAAGAAAA A T TIMP3 Ensembl:ENSG00000100234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:32814174..32814415 26863196 MeRIP-seq:(Medium) rs1181086784 Functional Loss SNV dbSNP153 33..33 33 - - - 90154 RMVar_ID_90154 Human_SNP_ID_702262562 m1A Human chr22 + 32859350 32859350 32859350 AGCTGGTACCGAGGATGGGCCCCCCCGGATAAAAGCATCATCAATGCCACAGACCCCTGAGCGCC AGCTGGTACCGAGGATGGGCCCCCCCGGATAAGAGCATCATCAATGCCACAGACCCCTGAGCGCC A G TIMP3 Ensembl:ENSG00000100234 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:32859301..32859425 26863196 MeRIP-seq:(Medium) rs779686845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22454622,Human_RBP_ID_22768269 RMVar_hsa_circ_104984,RMVar_hsa_circ_119519,RMVar_hsa_circ_119416,RMVar_hsa_circ_213951,RMVar_hsa_circ_103485,RMVar_hsa_circ_213952,RMVar_hsa_circ_213953,RMVar_hsa_circ_213954 90155 RMVar_ID_90155 Human_SNP_ID_702888103 m1A Human chr22 + 35257821 35257821 35257821 AACGGGGAAGGCGGGAAAGCTGCGGGGCCGGGAGGGGGCGTGCGGCCGCCCCGGGGGCCTGCGGA AACGGGGAAGGCGGGAAAGCTGCGGGGCCGGGTGGGGGCGTGCGGCCGCCCCGGGGGCCTGCGGA A T HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:35257813..35257980;chr22:35257815..35257978 26863196 MeRIP-seq:(Medium) rs1471895125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246588,Human_RBP_ID_5388196,Human_RBP_ID_8207315,Human_RBP_ID_9434163,Human_RBP_ID_18464182,Human_RBP_ID_22362487 90156 RMVar_ID_90156 Human_SNP_ID_702889300 m1A Human chr22 + 35262342 35262342 35262342 CTTTGTTTCTCAGACCTGGTCCTGTAGACGGGAAGGAGCCTGGACACAGTGACACATTCTCAAAG CTTTGTTTCTCAGACCTGGTCCTGTAGACGGGGAGGAGCCTGGACACAGTGACACATTCTCAAAG A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35262330..35262402 26863196 MeRIP-seq:(Medium) rs754098587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1610554,Human_RBP_ID_5504614,Human_RBP_ID_14464879,Human_RBP_ID_17701885,Human_RBP_ID_18787964 Human_Splice_Rec_2161272,Human_Splice_Rec_2161273,Human_Splice_Rec_2161296,Human_Splice_Rec_2161297,Human_Splice_Rec_2161323 RMVar_hsa_circ_213984,RMVar_hsa_circ_71981,RMVar_hsa_circ_323313,RMVar_hsa_circ_354267,RMVar_hsa_circ_356936,RMVar_hsa_circ_349233,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985 90157 RMVar_ID_90157 Human_SNP_ID_702890281 m1A Human chr22 + 35265578 35265578 35265578 TAGTGAAAAAAAAAAGAAAAAAGAAGAGAAGGACAAAGAGAGAGAGAGAGGAGAAAAGGTAAAGC TAGTGAAAAAAAAAAGAAAAAAGAAGAGAAGGCCAAAGAGAGAGAGAGAGGAGAAAAGGTAAAGC A C HMGXB4 Ensembl:ENSG00000100281 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35265527..35265639 26863196 MeRIP-seq:(Medium) rs71314937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65176 Human_Splice_Rec_2161281,Human_Splice_Rec_2161303 Human_miRNA_ID_2255812 RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_349233,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_213986,RMVar_hsa_circ_25441,RMVar_hsa_circ_302231 90158 RMVar_ID_90158 Human_SNP_ID_702898657 m1A Human chr22 + 35299948 35299948 35299948 GGCGGTAGCAGCAATGGACTTTCTCCTGGGGAACCCGTTCAGCTCTCCAGTGGGACAGCGCATCG GGCGGTAGCAGCAATGGACTTTCTCCTGGGGAGCCCGTTCAGCTCTCCAGTGGGACAGCGCATCG A G TOM1 Ensembl:ENSG00000100284 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:35299898..35300051 26863196 MeRIP-seq:(Medium) rs1277805815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930859,Human_RBP_ID_23119866 Human_Splice_Rec_2161383,Human_Splice_Rec_2161401,Human_Splice_Rec_2161429,Human_Splice_Rec_2161455,Human_Splice_Rec_2161487,Human_Splice_Rec_2161489,Human_Splice_Rec_2161503,Human_Splice_Rec_2161507,Human_Splice_Rec_2161519,Human_Splice_Rec_2161545,Human_Splice_Rec_2161555,Human_Splice_Rec_2161563 90159 RMVar_ID_90159 Human_SNP_ID_702904716 m1A Human chr22 - 35323591 35323591 35323591 GGTGTGTGGATGGGTGACAGCATGTCCAGGTCAGTCATGGGGAACTCCAGGCCTTTCCTCCGCAG GGTGTGTGGATGGGTGACAGCATGTCCAGGTCGGTCATGGGGAACTCCAGGCCTTTCCTCCGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35323540..35323628 26863196 MeRIP-seq:(Medium) rs1414639186 Functional Loss SNV dbSNP153 33..33 33 - - - 90160 RMVar_ID_90160 Human_SNP_ID_702920288 m1A Human chr22 + 35381150 35381150 35381150 TCCTCAGCGCAGCCGCCGCCCGCGGAGCCAGCACGAACGAGCCCAGCACCGGCCGGATGGAGCGT TCCTCAGCGCAGCCGCCGCCCGCGGAGCCAGCTCGAACGAGCCCAGCACCGGCCGGATGGAGCGT A T HMOX1 Ensembl:ENSG00000100292 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35381101..35381248 26863196 MeRIP-seq:(Medium) rs1229282612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392220 90161 RMVar_ID_90161 Human_SNP_ID_702926413 m1A Human chr22 + 35400199 35400199 35400199 GGTTCTTGTCTCCCCTGGTTTGTGAAGTGCGGAAAACCAGAGGTGAGGCTAGTGGGAGTGGGACT GGTTCTTGTCTCCCCTGGTTTGTGAAGTGCGGTAAACCAGAGGTGAGGCTAGTGGGAGTGGGACT A T MCM5 Ensembl:ENSG00000100297 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:35400126..35400271;chr22:35400126..35400625;chr22:35400126..35400382;chr22:35400126..35400327 26863196 MeRIP-seq:(Medium) rs1383585594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1942187,Human_RBP_ID_3671905,Human_RBP_ID_4708587,Human_RBP_ID_9332810,Human_RBP_ID_9348377,Human_RBP_ID_23212924 Human_Splice_Rec_2161635,Human_Splice_Rec_2161641,Human_Splice_Rec_2161671,Human_Splice_Rec_2161705 RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998 90162 RMVar_ID_90162 Human_SNP_ID_702926519 m1A Human chr22 + 35400463 35400463 35400463 GCGCAGTCATGTCGGGATTCGACGATCCTGGCATTTTCTACAGCGACAGCTTCGGGGGCGACGCC GCGCAGTCATGTCGGGATTCGACGATCCTGGCGTTTTCTACAGCGACAGCTTCGGGGGCGACGCC A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:35400424..35400643 26863196 MeRIP-seq:(Medium) rs761707670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1029168,Human_RBP_ID_1610635,Human_RBP_ID_1942188,Human_RBP_ID_4708588,Human_RBP_ID_9332812,Human_RBP_ID_18328979,Human_RBP_ID_18788038,Human_RBP_ID_19111956,Human_RBP_ID_22269205,Human_RBP_ID_22820278,Human_RBP_ID_23212753,Human_RBP_ID_27036164 Human_Splice_Rec_2161636,Human_Splice_Rec_2161642,Human_Splice_Rec_2161672,Human_Splice_Rec_2161706 RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000 90163 RMVar_ID_90163 Human_SNP_ID_702926521 m1A Human chr22 - 35400465 35400465 35400465 TGGGCGTCGCCCCCGAAGCTGTCGCTGTAGAAAATGCCAGGATCGTCGAATCCCGACATGACTGC TGGGCGTCGCCCCCGAAGCTGTCGCTGTAGAATATGCCAGGATCGTCGAATCCCGACATGACTGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:35400426..35400652;chr22:35400426..35400573 26863196 MeRIP-seq:(Medium) rs767484813 Functional Loss SNV dbSNP153 33..33 33 - - - 90164 RMVar_ID_90164 Human_SNP_ID_702927482 m1A Human chr22 + 35403516 35403516 35403516 AGGACATCCAGGTCATGCTCAAGTCGGACGCCAGCCCTTCCAGCATTCGTAGCCTGAAGGTGGGT AGGACATCCAGGTCATGCTCAAGTCGGACGCCGGCCCTTCCAGCATTCGTAGCCTGAAGGTGGGT A G MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:35403469..35408511 32194978 MeRIP-seq:(Medium) rs1437116502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_282183,Human_RBP_ID_1029173,Human_RBP_ID_7077900,Human_RBP_ID_14466093,Human_RBP_ID_18788054,Human_RBP_ID_26345348 Human_Splice_Rec_2161677,Human_Splice_Rec_2161713,Human_Splice_Rec_2161715 Human_miRNA_ID_173443 RMVar_hsa_circ_16862,RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000,RMVar_hsa_circ_112165,RMVar_hsa_circ_327159,RMVar_hsa_circ_338679,RMVar_hsa_circ_293240,RMVar_hsa_circ_38725,RMVar_hsa_circ_11891,RMVar_hsa_circ_214001,RMVar_hsa_circ_9546,RMVar_hsa_circ_15179,RMVar_hsa_circ_214002,RMVar_hsa_circ_214003,RMVar_hsa_circ_334658,RMVar_hsa_circ_336871,RMVar_hsa_circ_369922,RMVar_hsa_circ_90139,RMVar_hsa_circ_214004,RMVar_hsa_circ_214005 90165 RMVar_ID_90165 Human_SNP_ID_702928516 m1A Human chr22 + 35406620 35406620 35406620 CATCATCATCGCGGCCTCTGCGGTCCGTGCCAAGGCCACCCGCATCTCTATCCAGTGCCGCAGCT CATCATCATCGCGGCCTCTGCGGTCCGTGCCAGGGCCACCCGCATCTCTATCCAGTGCCGCAGCT A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35406502..35406646 26863196 MeRIP-seq:(Medium) rs1302606002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18194081 Human_Splice_Rec_2161646,Human_Splice_Rec_2161678,Human_Splice_Rec_2161714,Human_Splice_Rec_2161716 Human_miRNA_ID_594494,Human_miRNA_ID_1987300,Human_miRNA_ID_2218989,Human_miRNA_ID_3123820 RMVar_hsa_circ_16862,RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000,RMVar_hsa_circ_112165,RMVar_hsa_circ_327159,RMVar_hsa_circ_338679,RMVar_hsa_circ_38725,RMVar_hsa_circ_11891,RMVar_hsa_circ_214001,RMVar_hsa_circ_9546,RMVar_hsa_circ_15179,RMVar_hsa_circ_214002,RMVar_hsa_circ_214003,RMVar_hsa_circ_336871,RMVar_hsa_circ_369922,RMVar_hsa_circ_90139,RMVar_hsa_circ_110329,RMVar_hsa_circ_214004,RMVar_hsa_circ_214005,RMVar_hsa_circ_267908,RMVar_hsa_circ_268345,RMVar_hsa_circ_214006 90166 RMVar_ID_90166 Human_SNP_ID_702928542 m1A Human chr22 + 35406673 35406673 35406673 AGTGCCGCAGCTGCCGCAACACCCTCACCAACATTGCCATGCGCCCTGGCCTCGAGGGCTATGCC AGTGCCGCAGCTGCCGCAACACCCTCACCAACGTTGCCATGCGCCCTGGCCTCGAGGGCTATGCC A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:35406651..35406675 26863196 MeRIP-seq:(Medium) rs1349962902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65187,Human_RBP_ID_781312,Human_RBP_ID_3963212,Human_RBP_ID_8865699,Human_RBP_ID_18194081,Human_RBP_ID_18445387,Human_RBP_ID_18788057,Human_RBP_ID_19009057,Human_RBP_ID_22269217,Human_RBP_ID_22820286,Human_RBP_ID_26822441,Human_RBP_ID_27307205 Human_Splice_Rec_2161647,Human_Splice_Rec_2161679,Human_Splice_Rec_2161717 Human_miRNA_ID_2581927 RMVar_hsa_circ_16862,RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000,RMVar_hsa_circ_112165,RMVar_hsa_circ_327159,RMVar_hsa_circ_338679,RMVar_hsa_circ_38725,RMVar_hsa_circ_11891,RMVar_hsa_circ_214001,RMVar_hsa_circ_9546,RMVar_hsa_circ_15179,RMVar_hsa_circ_214002,RMVar_hsa_circ_214003,RMVar_hsa_circ_336871,RMVar_hsa_circ_369922,RMVar_hsa_circ_90139,RMVar_hsa_circ_110329,RMVar_hsa_circ_214004,RMVar_hsa_circ_214005,RMVar_hsa_circ_267908,RMVar_hsa_circ_268345,RMVar_hsa_circ_214006 90167 RMVar_ID_90167 Human_SNP_ID_702928557 m1A Human chr22 + 35406701 35406701 35406701 CAACATTGCCATGCGCCCTGGCCTCGAGGGCTATGCCCTGCCCAGGAAGTGCAACACGTGAGTCT CAACATTGCCATGCGCCCTGGCCTCGAGGGCTGTGCCCTGCCCAGGAAGTGCAACACGTGAGTCT A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:35406651..35406750 26863196 MeRIP-seq:(Medium) rs748716384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245935,Human_RBP_ID_578938,Human_RBP_ID_781312,Human_RBP_ID_3963212,Human_RBP_ID_5388210,Human_RBP_ID_8865699,Human_RBP_ID_9348378,Human_RBP_ID_18194081,Human_RBP_ID_18788057,Human_RBP_ID_19009057 Human_Splice_Rec_2161647,Human_Splice_Rec_2161679,Human_Splice_Rec_2161717 Human_miRNA_ID_2041835,Human_miRNA_ID_2696378,Human_miRNA_ID_3020812 RMVar_hsa_circ_16862,RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000,RMVar_hsa_circ_112165,RMVar_hsa_circ_327159,RMVar_hsa_circ_338679,RMVar_hsa_circ_38725,RMVar_hsa_circ_11891,RMVar_hsa_circ_214001,RMVar_hsa_circ_9546,RMVar_hsa_circ_15179,RMVar_hsa_circ_214002,RMVar_hsa_circ_214003,RMVar_hsa_circ_336871,RMVar_hsa_circ_369922,RMVar_hsa_circ_90139,RMVar_hsa_circ_110329,RMVar_hsa_circ_214004,RMVar_hsa_circ_214005,RMVar_hsa_circ_267908,RMVar_hsa_circ_268345,RMVar_hsa_circ_214006 90168 RMVar_ID_90168 Human_SNP_ID_702928571 m1A Human chr22 - 35406727 35406725 35406727 CACCTCCCACAGTCCCTCTGGGCCACAGACTCACGTGTTGCACTTCCTGGGCAGGGCATAGCCCT CACCTCCCACAGTCCCTCTGGGCCACAGACTC__GTGTTGCACTTCCTGGGCAGGGCATAGCCCT CGT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:35406678..35409525 32194978 MeRIP-seq:(Medium) rs1302705119 Functional Loss DEL dbSNP153 33..34 33 - - - 90169 RMVar_ID_90169 Human_SNP_ID_702932712 m1A Human chr22 - 35421304 35421304 35421304 CACAATGGCCTCCAGCTGCCTGTGGGGGCAACAGCGTGCTCAGGGTAGCCTCGGTCCGCTATTCC CACAATGGCCTCCAGCTGCCTGTGGGGGCAACGGCGTGCTCAGGGTAGCCTCGGTCCGCTATTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35421301..35421325 26863196 MeRIP-seq:(Medium) rs772610008 Functional Loss SNV dbSNP153 33..33 33 - - - 90170 RMVar_ID_90170 Human_SNP_ID_702933014 m1A Human chr22 + 35422207 35422207 35422207 GTTCTAGTTGGGGAGAGATAGACAGTAGAGAAACAAATGCAGGTAGTGTAGGTAGTGAAAAAGGC GTTCTAGTTGGGGAGAGATAGACAGTAGAGAACCAAATGCAGGTAGTGTAGGTAGTGAAAAAGGC A C MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35422202..35422441 26863196 MeRIP-seq:(Medium) rs71314942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14466444 RMVar_hsa_circ_338679,RMVar_hsa_circ_214003,RMVar_hsa_circ_113387,RMVar_hsa_circ_214011,RMVar_hsa_circ_369765,RMVar_hsa_circ_103796,RMVar_hsa_circ_111102,RMVar_hsa_circ_127853,RMVar_hsa_circ_214013,RMVar_hsa_circ_214015,RMVar_hsa_circ_214014,RMVar_hsa_circ_281293,RMVar_hsa_circ_214017,RMVar_hsa_circ_214018,RMVar_hsa_circ_214019,RMVar_hsa_circ_85612 90171 RMVar_ID_90171 Human_SNP_ID_702933301 m1A Human chr22 + 35423325 35423325 35423325 TGGCTCCCAGGTGTCTGAGCACAGCATCATCAAGGACTTCACCAAGCAGGTGAGCCTGCCTTGGA TGGCTCCCAGGTGTCTGAGCACAGCATCATCAGGGACTTCACCAAGCAGGTGAGCCTGCCTTGGA A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:35423276..35423350 32194978 MeRIP-seq:(Medium) rs1325457588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_282184,Human_RBP_ID_1610749,Human_RBP_ID_1942208,Human_RBP_ID_5119912,Human_RBP_ID_8549116,Human_RBP_ID_14466487,Human_RBP_ID_18788101,Human_RBP_ID_19009066,Human_RBP_ID_22086524,Human_RBP_ID_22454934 Human_Splice_Rec_2161669,Human_Splice_Rec_2161701 RMVar_hsa_circ_338679,RMVar_hsa_circ_214003,RMVar_hsa_circ_113387,RMVar_hsa_circ_214011,RMVar_hsa_circ_369765,RMVar_hsa_circ_103796,RMVar_hsa_circ_111102,RMVar_hsa_circ_127853,RMVar_hsa_circ_214013,RMVar_hsa_circ_214015,RMVar_hsa_circ_214014,RMVar_hsa_circ_281293,RMVar_hsa_circ_214017,RMVar_hsa_circ_214018 90172 RMVar_ID_90172 Human_SNP_ID_702934071 m1A Human chr22 + 35426294 35426294 35426294 AGCCAGGGAAACACCTGCTTGTTGGGGAAAGCAAAGGCTGAGGAGAGAGCCTGAAGGGAGGCCAG AGCCAGGGAAACACCTGCTTGTTGGGGAAAGCGAAGGCTGAGGAGAGAGCCTGAAGGGAGGCCAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:35426243..35426372 26863196 MeRIP-seq:(Medium) rs1444604171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14466637 90173 RMVar_ID_90173 Human_SNP_ID_702937113 m1A Human chr22 + 35437429 35437429 35437429 GGTGGGCCAGCAGCCATCATCATGCCATGTAGACAGAGCCTACGTGGGAATGAAACTGATACACT GGTGGGCCAGCAGCCATCATCATGCCATGTAGGCAGAGCCTACGTGGGAATGAAACTGATACACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:35437325..35437450 26863196 MeRIP-seq:(Medium) rs1431642079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8549164,Human_RBP_ID_14467101 90174 RMVar_ID_90174 Human_SNP_ID_702941807 m1A Human chr22 + 35453440 35453439 35453441 AGAGTGATTCAGAGAGACACAGAGACAGAGACAGGGACAGAGAGATAGAAACAGAGACAGAGAAA AGAGTGATTCAGAGAGACACAGAGACAGAGAC__GGACAGAGAGATAGAAACAGAGACAGAGAAA CAG C lnc-MCM5-1,lnc-MCM5-1:2 RNACentral:URS00008B3FDF,RNACentral:URS00008B6D52 lincRNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:35453369..35453534 26863196 MeRIP-seq:(Medium) rs1388795583 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14467543 90175 RMVar_ID_90175 Human_SNP_ID_702941813 m1A Human chr22 + 35453452 35453449 35453453 AGAGACACAGAGACAGAGACAGGGACAGAGAGATAGAAACAGAGACAGAGAAAGAGACAGAGGGA AGAGACACAGAGACAGAGACAGGGACAGAG____AGAAACAGAGACAGAGAAAGAGACAGAGGGA GAGAT G lnc-MCM5-1,lnc-MCM5-1:2 RNACentral:URS00008B3FDF,RNACentral:URS00008B6D52 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35453376..35453778 26863196 MeRIP-seq:(Medium) rs1434185854 Functional Loss DEL dbSNP153 31..34 33 - - - 90176 RMVar_ID_90176 Human_SNP_ID_702950481 m1A Human chr22 - 35483954 35483954 35483954 TTGCTGACAGGGCATGGGTACAGAAGACCTCAATTACATACACTTAAGAATCCTCCCTTCCTCCC TTGCTGACAGGGCATGGGTACAGAAGACCTCAGTTACATACACTTAAGAATCCTCCCTTCCTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35483919..35484069 26863196 MeRIP-seq:(Medium) rs1038200307 Functional Loss SNV dbSNP153 33..33 33 - - - 90177 RMVar_ID_90177 Human_SNP_ID_702972819 m1A Human chr22 + 35571378 35571378 35571378 AGACCTCCTTGCTGTGCCTCCAACTCACAGGTACAGGCAGCCACAGGGCCTTGGTACCTGCTTTC AGACCTCCTTGCTGTGCCTCCAACTCACAGGTGCAGGCAGCCACAGGGCCTTGGTACCTGCTTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35571340..35571482 26863196 MeRIP-seq:(Medium) rs997502639 Functional Loss SNV dbSNP153 33..33 33 - - - 90178 RMVar_ID_90178 Human_SNP_ID_702977117 m1A Human chr22 - 35587531 35587531 35587531 CAGTGAGCTCTTCCAGGCCCCCAGTGAGCCTGAGAGGGGGTCTGGGAAGAGTCAAGAGACACCCA CAGTGAGCTCTTCCAGGCCCCCAGTGAGCCTGGGAGGGGGTCTGGGAAGAGTCAAGAGACACCCA T C HSALNG0135166 RNACentral:URS0000EBC9A2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35587480..35587627 26863196 MeRIP-seq:(Medium) rs749454048 Functional Loss SNV dbSNP153 33..33 33 - - - 90179 RMVar_ID_90179 Human_SNP_ID_702985362 m1A Human chr22 + 35617229 35617229 35617229 CAGCCTCCACCTTCCCCCAGACGTTCAGCACCAACTGCCATTCCCCGTCGCTGAGCCCCATGGCG CAGCCTCCACCTTCCCCCAGACGTTCAGCACCCACTGCCATTCCCCGTCGCTGAGCCCCATGGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35617134..35617279 26863196 MeRIP-seq:(Medium) rs1369440161 Functional Loss SNV dbSNP153 33..33 33 - - - 90180 RMVar_ID_90180 Human_SNP_ID_702986683 m1A Human chr22 - 35622458 35622458 35622458 AAGGGGAGCTGTGGTCAGTATGATGGATGCTGAGGGGCTGGAGAGGAGCAGCCCTGGTGGGTGGG AAGGGGAGCTGTGGTCAGTATGATGGATGCTGGGGGGCTGGAGAGGAGCAGCCCTGGTGGGTGGG T C MB Ensembl:ENSG00000198125 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:35622448..35622519 26863196 MeRIP-seq:(Medium) rs997643841 Functional Loss SNV dbSNP153 33..33 33 - - - 90181 RMVar_ID_90181 Human_SNP_ID_703018290 m1A Human chr22 + 35739133 35739133 35739133 GTGATTCTGGGGGAGGACGGGAGGGGAGAGAGAAGGCTAGGTGGTCGATTACACAAGCATCCCAT GTGATTCTGGGGGAGGACGGGAGGGGAGAGAGGAGGCTAGGTGGTCGATTACACAAGCATCCCAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:35738884..35739135 32194978 MeRIP-seq:(Medium) rs1206242644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214029 90182 RMVar_ID_90182 Human_SNP_ID_703019234 m1A Human chr22 - 35742968 35742968 35742968 GGAATTTTCATCTTCCAGAGCCTTTATGAGTCACTTCTCTATCCACAGTCTTGAGCCTGTGGCTA GGAATTTTCATCTTCCAGAGCCTTTATGAGTCTCTTCTCTATCCACAGTCTTGAGCCTGTGGCTA T A RBFOX2 Ensembl:ENSG00000100320 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:35742920..35743120 32194978 MeRIP-seq:(Medium) rs751517601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17285792,Human_RBP_ID_17399007,Human_RBP_ID_17514989,Human_RBP_ID_20755358,Human_RBP_ID_27708198 Human_miRNA_ID_251614,Human_miRNA_ID_861403 RMVar_hsa_circ_87412,RMVar_hsa_circ_214028 90183 RMVar_ID_90183 Human_SNP_ID_703027043 m1A Human chr22 - 35778067 35778067 35778067 TTTTTATTTTTATCTCTGCAGCAGTTTGGCAAAATCCTAGATGTAGAAATAATCTTTAATGAACG TTTTTATTTTTATCTCTGCAGCAGTTTGGCAAGATCCTAGATGTAGAAATAATCTTTAATGAACG T C RBFOX2 Ensembl:ENSG00000100320 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:35778065..35781686 32194978 MeRIP-seq:(Medium) rs765286376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65220,Human_RBP_ID_14469546,Human_RBP_ID_25667559 Human_Splice_Rec_2161838,Human_Splice_Rec_2161839,Human_Splice_Rec_2161862,Human_Splice_Rec_2161863,Human_Splice_Rec_2161884,Human_Splice_Rec_2161885,Human_Splice_Rec_2161904,Human_Splice_Rec_2161905,Human_Splice_Rec_2161946,Human_Splice_Rec_2161947,Human_Splice_Rec_2161970,Human_Splice_Rec_2161971,Human_Splice_Rec_2162000,Human_Splice_Rec_2162001,Human_Splice_Rec_2162019,Human_Splice_Rec_2162042,Human_Splice_Rec_2162043,Human_Splice_Rec_2162060,Human_Splice_Rec_2162061,Human_Splice_Rec_2162068,Human_Splice_Rec_2162076 RMVar_hsa_circ_2310,RMVar_hsa_circ_214033,RMVar_hsa_circ_117518,RMVar_hsa_circ_214034,RMVar_hsa_circ_36549,RMVar_hsa_circ_111055,RMVar_hsa_circ_214039,RMVar_hsa_circ_18951,RMVar_hsa_circ_281089,RMVar_hsa_circ_214041 90184 RMVar_ID_90184 Human_SNP_ID_703027835 m1A Human chr22 - 35781715 35781715 35781715 GCAGACAGAAGGTGGAGCACAGACAGACGGCCAGCAGTCACAGACACAAAGTAGTGAAAATTCAG GCAGACAGAAGGTGGAGCACAGACAGACGGCCGGCAGTCACAGACACAAAGTAGTGAAAATTCAG T C RBFOX2 Ensembl:ENSG00000100320 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35781601..35781750 26863196 MeRIP-seq:(Medium) rs779335878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65221,Human_RBP_ID_245960 Human_Splice_Rec_2161836,Human_Splice_Rec_2161860,Human_Splice_Rec_2161882,Human_Splice_Rec_2161902,Human_Splice_Rec_2161924,Human_Splice_Rec_2161944,Human_Splice_Rec_2161968,Human_Splice_Rec_2161998,Human_Splice_Rec_2162040,Human_Splice_Rec_2162058,Human_Splice_Rec_2162066,Human_Splice_Rec_2162074 RMVar_hsa_circ_2310,RMVar_hsa_circ_117518,RMVar_hsa_circ_214034,RMVar_hsa_circ_111055,RMVar_hsa_circ_214041 90185 RMVar_ID_90185 Human_SNP_ID_703034491 m1A Human chr22 - 35809897 35809897 35809897 CAGAATGGAATTCCCACAGAGTATGGGGTGCCACACACTCAAGACTATGCCGGCCAGACCGGTGA CAGAATGGAATTCCCACAGAGTATGGGGTGCCGCACACTCAAGACTATGCCGGCCAGACCGGTGA T C RBFOX2 Ensembl:ENSG00000100320 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:35809846..35810062 26863196 MeRIP-seq:(Medium) rs567688413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579124,Human_RBP_ID_17515001 Human_miRNA_ID_2076764,Human_miRNA_ID_2076765,Human_miRNA_ID_2866718,Human_miRNA_ID_2866719,Human_miRNA_ID_2910880,Human_miRNA_ID_2910881 RMVar_hsa_circ_111055,RMVar_hsa_circ_214042,RMVar_hsa_circ_337746,RMVar_hsa_circ_214041,RMVar_hsa_circ_279162 90186 RMVar_ID_90186 Human_SNP_ID_703034507 m1A Human chr22 - 35809945 35809945 35809945 GACGCAATGGTTCAGCCTTTTACTACCATCCCATTTCCACCACCTCCGCAGAATGGAATTCCCAC GACGCAATGGTTCAGCCTTTTACTACCATCCCTTTTCCACCACCTCCGCAGAATGGAATTCCCAC T A RBFOX2 Ensembl:ENSG00000100320 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:35809851..35810025 32194978 MeRIP-seq:(Medium) rs955375463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65223,Human_RBP_ID_4694766,Human_RBP_ID_17020738,Human_RBP_ID_17285810,Human_RBP_ID_17399026,Human_RBP_ID_17515002,Human_RBP_ID_17985496,Human_RBP_ID_23945220 Human_Splice_Rec_2161834,Human_Splice_Rec_2161858,Human_Splice_Rec_2161880,Human_Splice_Rec_2161900,Human_Splice_Rec_2161922,Human_Splice_Rec_2161966,Human_Splice_Rec_2161996,Human_Splice_Rec_2162038,Human_Splice_Rec_2162056,Human_Splice_Rec_2162064,Human_Splice_Rec_2162072 RMVar_hsa_circ_111055,RMVar_hsa_circ_214042,RMVar_hsa_circ_337746,RMVar_hsa_circ_214041,RMVar_hsa_circ_279162 90187 RMVar_ID_90187 Human_SNP_ID_703041789 m1A Human chr22 + 35840307 35840307 35840307 ACAGCTTTCTTTTCCACCCCCCTCCCCCCCCAATCTAGCTATTTAAGGGTGGGTAATTGATCTCT ACAGCTTTCTTTTCCACCCCCCTCCCCCCCCAGTCTAGCTATTTAAGGGTGGGTAATTGATCTCT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:35840259..35840388 26863196 MeRIP-seq:(Medium) rs369246611 Functional Loss SNV dbSNP153 33..33 33 - - - 90188 RMVar_ID_90188 Human_SNP_ID_703041790 m1A Human chr22 + 35840307 35840307 35840307 ACAGCTTTCTTTTCCACCCCCCTCCCCCCCCAATCTAGCTATTTAAGGGTGGGTAATTGATCTCT ACAGCTTTCTTTTCCACCCCCCTCCCCCCCCATTCTAGCTATTTAAGGGTGGGTAATTGATCTCT A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:35840259..35840388 26863196 MeRIP-seq:(Medium) rs369246611 Functional Loss SNV dbSNP153 33..33 33 - - - 90189 RMVar_ID_90189 Human_SNP_ID_703079912 m1A Human chr22 + 36004208 36004208 36004208 AATTTGCCCAGAGTTTCAATGCTTAGGCCTAGATCGTTTCAACATTCAAGTTGACAACACTTTCA AATTTGCCCAGAGTTTCAATGCTTAGGCCTAGGTCGTTTCAACATTCAAGTTGACAACACTTTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36004206..36004418 26863196 MeRIP-seq:(Medium) rs1475618622 Functional Loss SNV dbSNP153 33..33 33 - - - 90190 RMVar_ID_90190 Human_SNP_ID_703084748 m1A Human chr22 + 36025237 36025237 36025237 GCTATTAATACATTGGTCTCCTGTTTCCAAACAAACCAAGCAGTCTTTCTCAATGCCTGTGCACC GCTATTAATACATTGGTCTCCTGTTTCCAAACCAACCAAGCAGTCTTTCTCAATGCCTGTGCACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36025234..36025421 26863196 MeRIP-seq:(Medium) rs1338706224 Functional Loss SNV dbSNP153 33..33 33 - - - 90191 RMVar_ID_90191 Human_SNP_ID_703085899 m1A Human chr22 - 36028746 36028746 36028746 TGAGCCAGCGCGGCCGGTGGGCGAGCTCCGGGAGTGCGAGAGGCGGGGCGGCGCGGCGGGCCGGG TGAGCCAGCGCGGCCGGTGGGCGAGCTCCGGGTGTGCGAGAGGCGGGGCGGCGCGGCGGGCCGGG T A RBFOX2 Ensembl:ENSG00000100320 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36028326..36028827 26863196 MeRIP-seq:(Medium) rs1375383506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579140,Human_RBP_ID_4694819 90192 RMVar_ID_90192 Human_SNP_ID_703085900 m1A Human chr22 - 36028746 36028746 36028746 TGAGCCAGCGCGGCCGGTGGGCGAGCTCCGGGAGTGCGAGAGGCGGGGCGGCGCGGCGGGCCGGG TGAGCCAGCGCGGCCGGTGGGCGAGCTCCGGGGGTGCGAGAGGCGGGGCGGCGCGGCGGGCCGGG T C RBFOX2 Ensembl:ENSG00000100320 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36028326..36028827 26863196 MeRIP-seq:(Medium) rs1375383506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579140,Human_RBP_ID_4694819 90193 RMVar_ID_90193 Human_SNP_ID_703138315 m1A Human chr22 - 36226448 36226448 36226448 GTCCCCTGCTTGAACCCTGAGAGGCAGGTGGTAGGCCATGGCCACAATCCCCAGCTGAGGAGCAG GTCCCCTGCTTGAACCCTGAGAGGCAGGTGGTGGGCCATGGCCACAATCCCCAGCTGAGGAGCAG T C APOL2 Ensembl:ENSG00000128335 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:36226397..36226498 32194978 MeRIP-seq:(Medium) rs772076302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2727896 RMVar_hsa_circ_214045,RMVar_hsa_circ_82378 90194 RMVar_ID_90194 Human_SNP_ID_703139309 m1A Human chr22 - 36229085 36229084 36229085 TAAACTGATTTGGGGAGATTCTTGCTGAGCCAAGGTGGTGCAAGTCCAGAAAGCAGTGGGTGAGT TAAACTGATTTGGGGAGATTCTTGCTGAGCCA_GGTGGTGCAAGTCCAGAAAGCAGTGGGTGAGT CT C APOL2 Ensembl:ENSG00000128335 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36229076..36229269 26863196 MeRIP-seq:(Medium) rs1339065017 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_214045,RMVar_hsa_circ_82378 90195 RMVar_ID_90195 Human_SNP_ID_703139312 m1A Human chr22 - 36229085 36229085 36229085 TAAACTGATTTGGGGAGATTCTTGCTGAGCCAAGGTGGTGCAAGTCCAGAAAGCAGTGGGTGAGT TAAACTGATTTGGGGAGATTCTTGCTGAGCCATGGTGGTGCAAGTCCAGAAAGCAGTGGGTGAGT T A APOL2 Ensembl:ENSG00000128335 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36229076..36229269 26863196 MeRIP-seq:(Medium) rs533794126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214045,RMVar_hsa_circ_82378 90196 RMVar_ID_90196 Human_SNP_ID_703139334 m1A Human chr22 - 36229154 36229154 36229154 AGTGGTGGGGGTGAGGAGCATGATCAGATAACAAACGGTGCTCAGACAGCAAGCGGGGAGGACCC AGTGGTGGGGGTGAGGAGCATGATCAGATAACGAACGGTGCTCAGACAGCAAGCGGGGAGGACCC T C APOL2 Ensembl:ENSG00000128335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36229152..36229235 26863196 MeRIP-seq:(Medium) rs545561873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214045,RMVar_hsa_circ_82378 90197 RMVar_ID_90197 Human_SNP_ID_703141397 m1A Human chr22 + 36236621 36236621 36236621 TTCTCACCTTGTGTCTCTGCGCACTCCCCGGCACACCCACTTCCAGCAGCTGGTCTTTGTTTGCA TTCTCACCTTGTGTCTCTGCGCACTCCCCGGCTCACCCACTTCCAGCAGCTGGTCTTTGTTTGCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36236615..36236755 26863196 MeRIP-seq:(Medium) rs1209658540 Functional Loss SNV dbSNP153 33..33 33 - - - 90198 RMVar_ID_90198 Human_SNP_ID_703142249 m1A Human chr22 - 36239499 36239499 36239499 GGTTATTACACAGATGCACAGCTGGACGTGGGATCCACACAGCTCAGAACAGTTGGATCTTGCTC GGTTATTACACAGATGCACAGCTGGACGTGGGTTCCACACAGCTCAGAACAGTTGGATCTTGCTC T A APOL2 Ensembl:ENSG00000128335 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36239407..36239523 26863196 MeRIP-seq:(Medium) rs774112437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23015260 Human_Splice_Rec_2162275,Human_Splice_Rec_2162284,Human_Splice_Rec_2162285,Human_Splice_Rec_2162293,Human_Splice_Rec_2162311,Human_Splice_Rec_2162323,Human_Splice_Rec_2162326,Human_Splice_Rec_2162327,Human_Splice_Rec_2162329 90199 RMVar_ID_90199 Human_SNP_ID_703142250 m1A Human chr22 - 36239499 36239499 36239499 GGTTATTACACAGATGCACAGCTGGACGTGGGATCCACACAGCTCAGAACAGTTGGATCTTGCTC GGTTATTACACAGATGCACAGCTGGACGTGGGGTCCACACAGCTCAGAACAGTTGGATCTTGCTC T C APOL2 Ensembl:ENSG00000128335 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36239407..36239523 26863196 MeRIP-seq:(Medium) rs774112437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23015260 Human_Splice_Rec_2162275,Human_Splice_Rec_2162284,Human_Splice_Rec_2162285,Human_Splice_Rec_2162293,Human_Splice_Rec_2162311,Human_Splice_Rec_2162323,Human_Splice_Rec_2162326,Human_Splice_Rec_2162327,Human_Splice_Rec_2162329 90200 RMVar_ID_90200 Human_SNP_ID_703142256 m1A Human chr22 - 36239506 36239506 36239506 CGTGTCTGGTTATTACACAGATGCACAGCTGGACGTGGGATCCACACAGCTCAGAACAGTTGGAT CGTGTCTGGTTATTACACAGATGCACAGCTGGGCGTGGGATCCACACAGCTCAGAACAGTTGGAT T C APOL2 Ensembl:ENSG00000128335 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:36239433..36239540;chr22:36239415..36239614 26863196 MeRIP-seq:(Medium) rs931103295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23015260 Human_Splice_Rec_2162275,Human_Splice_Rec_2162284,Human_Splice_Rec_2162285,Human_Splice_Rec_2162293,Human_Splice_Rec_2162311,Human_Splice_Rec_2162323,Human_Splice_Rec_2162326,Human_Splice_Rec_2162327,Human_Splice_Rec_2162329 90201 RMVar_ID_90201 Human_SNP_ID_703154055 m1A Human chr22 + 36282031 36282031 36282031 GAGACATTTTAGAATCAGGAGGGAGACAGCGGACAGTGGCGCTGCCTGGGACAGGGTGGGGAGGA GAGACATTTTAGAATCAGGAGGGAGACAGCGGGCAGTGGCGCTGCCTGGGACAGGGTGGGGAGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr22:36281984..36282127;chr22:36281676..36284275 26863196,32194978 MeRIP-seq:(Medium) rs910336450 Functional Loss SNV dbSNP153 33..33 33 - - - 90202 RMVar_ID_90202 Human_SNP_ID_703154134 m1A Human chr22 + 36282282 36282282 36282282 CAGGGAGGCTGACGACTGCGGGGGCTCCGACTACCAAAAGGCCTCAGTCTGAAGAAAAATAGATT CAGGGAGGCTGACGACTGCGGGGGCTCCGACTCCCAAAAGGCCTCAGTCTGAAGAAAAATAGATT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:36282232..36282500 26863196 MeRIP-seq:(Medium) rs922704439 Functional Loss SNV dbSNP153 33..33 33 - - - 90203 RMVar_ID_90203 Human_SNP_ID_703154186 m1A Human chr22 + 36282473 36282473 36282473 GTATCAGATTCTGAGCAGGGGAGGGAGCTGGAAGGGGATGCAGCAGAGGAAGCCAAATGCCCTCA GTATCAGATTCTGAGCAGGGGAGGGAGCTGGAGGGGGATGCAGCAGAGGAAGCCAAATGCCCTCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:36282426..36282500 32194978 MeRIP-seq:(Medium) rs771229879 Functional Loss SNV dbSNP153 33..33 33 - - - 90204 RMVar_ID_90204 Human_SNP_ID_703154218 m1A Human chr22 - 36282561 36282561 36282561 CCTCTCCCCACCTTCTTGGGACTGCTGTGAACATGCCTCCTCCTGCCCTCCGCCCCGTCCCCCCA CCTCTCCCCACCTTCTTGGGACTGCTGTGAACGTGCCTCCTCCTGCCCTCCGCCCCGTCCCCCCA T C MYH9 Ensembl:ENSG00000100345 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36282051..36282665 26863196 MeRIP-seq:(Medium) rs886057476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65245,Human_RBP_ID_245985,Human_RBP_ID_579188,Human_RBP_ID_4694927,Human_RBP_ID_8549452,Human_RBP_ID_18952567,Human_RBP_ID_23012830,Human_RBP_ID_24493994,Human_RBP_ID_27493510 Human_miRNA_ID_2476949,Human_miRNA_ID_2962732 Clinvar_Rec_508,Clinvar_Rec_4478 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_111268,RMVar_hsa_circ_121277,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214056,RMVar_hsa_circ_214057,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047 90205 RMVar_ID_90205 Human_SNP_ID_703154730 m1A Human chr22 - 36284148 36284148 36284148 GCCGGAAACTGCAGCGCGAGCTGGAGGACGCCACTGAGACGGCCGATGCCATGAACCGCGAAGTC GCCGGAAACTGCAGCGCGAGCTGGAGGACGCCGCTGAGACGGCCGATGCCATGAACCGCGAAGTC T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36284101..36284212 26863196 MeRIP-seq:(Medium) rs754138115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4694942,Human_RBP_ID_22768284 Human_Splice_Rec_2162525 RMVar_hsa_circ_3438,RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_121277,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214056,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_267240 90206 RMVar_ID_90206 Human_SNP_ID_703154740 m1A Human chr22 - 36284175 36284175 36284175 AGGAGGCCCAGCGGGCCAACGCCTCCCGCCGGAAACTGCAGCGCGAGCTGGAGGACGCCACTGAG AGGAGGCCCAGCGGGCCAACGCCTCCCGCCGGCAACTGCAGCGCGAGCTGGAGGACGCCACTGAG T G MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36284151..36284175 26863196 MeRIP-seq:(Medium) rs1180813769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22454648,Human_RBP_ID_22768284 Human_Splice_Rec_2162524,Human_Splice_Rec_2162525 RMVar_hsa_circ_3438,RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_121277,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214056,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_267240 90207 RMVar_ID_90207 Human_SNP_ID_703154767 m1A Human chr22 - 36284250 36284250 36284250 CACGTCCATCTCCGCAGGCCGACAAGGCATCTACCCGCCTGAAGCAGCTCAAGCGGCAGCTGGAG CACGTCCATCTCCGCAGGCCGACAAGGCATCTGCCCGCCTGAAGCAGCTCAAGCGGCAGCTGGAG T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36284201..36284275 26863196 MeRIP-seq:(Medium) rs958621472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65247,Human_RBP_ID_579191,Human_RBP_ID_930892,Human_RBP_ID_4694950,Human_RBP_ID_8235691,Human_RBP_ID_9392237,Human_RBP_ID_24381253 Human_Splice_Rec_2162524,Human_Splice_Rec_2162534 RMVar_hsa_circ_3438,RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_121277,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214056,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_267240 90208 RMVar_ID_90208 Human_SNP_ID_703154773 m1A Human chr22 - 36284267 36284267 36284267 ACCGGGGCCACGGGCCACACGTCCATCTCCGCAGGCCGACAAGGCATCTACCCGCCTGAAGCAGC ACCGGGGCCACGGGCCACACGTCCATCTCCGCGGGCCGACAAGGCATCTACCCGCCTGAAGCAGC T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36284226..36284275 26863196 MeRIP-seq:(Medium) rs916938077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65247,Human_RBP_ID_579191,Human_RBP_ID_5203329,Human_RBP_ID_24381253 Human_Splice_Rec_2162534 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_267240 90209 RMVar_ID_90209 Human_SNP_ID_703155266 m1A Human chr22 - 36285707 36285692 36285707 CGCCCAGCTGGAGGAGGAGCTGGAGGAGGAGCAGGGCAACACGGAGCTGATCAACGACCGGCTGA CGCCCAGCTGGAGGAGGAGCTGGAGGAGGAGC_______________TGATCAACGACCGGCTGA AGCTCCGTGTTGCCCT A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36285651..36285725 26863196 MeRIP-seq:(Medium) rs876657893 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_65250,Human_RBP_ID_833702,Human_RBP_ID_9392243,Human_RBP_ID_17701909,Human_RBP_ID_26344909 Human_Splice_Rec_2162518,Human_Splice_Rec_2162519,Human_Splice_Rec_2162528,Human_Splice_Rec_2162529,Human_Splice_Rec_2162536,Human_Splice_Rec_2162537 Human_miRNA_ID_865367,Human_miRNA_ID_2381713,Human_miRNA_ID_2465327,Human_miRNA_ID_3024722,Human_miRNA_ID_3091455 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_75874,RMVar_hsa_circ_95666,RMVar_hsa_circ_105916,RMVar_hsa_circ_214058,RMVar_hsa_circ_214059,RMVar_hsa_circ_108000,RMVar_hsa_circ_112684,RMVar_hsa_circ_106579,RMVar_hsa_circ_214062,RMVar_hsa_circ_214063,RMVar_hsa_circ_214064,RMVar_hsa_circ_214061,RMVar_hsa_circ_52385,RMVar_hsa_circ_268156,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066 90210 RMVar_ID_90210 Human_SNP_ID_703156436 m1A Human chr22 - 36289168 36289168 36289168 TGGCCCGGGCCCTGGAGGAAGCCATGGAGCAGAAGGCGGAGCTGGAGCGGCTCAACAAGCAGTTC TGGCCCGGGCCCTGGAGGAAGCCATGGAGCAGGAGGCGGAGCTGGAGCGGCTCAACAAGCAGTTC T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:36289068..36289281 26863196 MeRIP-seq:(Medium) rs750188842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65255,Human_RBP_ID_4695006,Human_RBP_ID_9392265,Human_RBP_ID_26345941 Human_Splice_Rec_2162509 Clinvar_Rec_509 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_108000,RMVar_hsa_circ_112684,RMVar_hsa_circ_214063,RMVar_hsa_circ_214064,RMVar_hsa_circ_58298,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069 90211 RMVar_ID_90211 Human_SNP_ID_703157395 m1A Human chr22 - 36291997 36291994 36291997 AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAGAAGTTTGACCAGGTGTGTGGCCGTTGGCCCCAT AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAG___TTTGACCAGGTGTGTGGCCGTTGGCCCCAT ACTT A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36291976..36292000 26863196 MeRIP-seq:(Medium) rs889313598 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5599391,Human_RBP_ID_22087347 Human_Splice_Rec_2162507 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072 90212 RMVar_ID_90212 Human_SNP_ID_703157399 m1A Human chr22 - 36291997 36291997 36291997 AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAGAAGTTTGACCAGGTGTGTGGCCGTTGGCCCCAT AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAGTAGTTTGACCAGGTGTGTGGCCGTTGGCCCCAT T A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36291976..36292000 26863196 MeRIP-seq:(Medium) rs1486787362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5599391,Human_RBP_ID_22087347 Human_Splice_Rec_2162507 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072 90213 RMVar_ID_90213 Human_SNP_ID_703157476 m1A Human chr22 - 36292168 36292168 36292168 TGGGGTGCCTGGAAACTGCTGAGGAGGTGAAGAGGAAGCTCCAGAAGGACCTGGAGGGCCTGAGC TGGGGTGCCTGGAAACTGCTGAGGAGGTGAAGTGGAAGCTCCAGAAGGACCTGGAGGGCCTGAGC T A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:36291889..36292250 26863196 MeRIP-seq:(Medium) rs757468108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65257,Human_RBP_ID_211780,Human_RBP_ID_833704,Human_RBP_ID_8549459,Human_RBP_ID_9300690,Human_RBP_ID_9333352,Human_RBP_ID_9392273,Human_RBP_ID_18194340,Human_RBP_ID_18413186,Human_RBP_ID_22086526,Human_RBP_ID_22723956,Human_RBP_ID_24547083,Human_RBP_ID_26344918 Human_Splice_Rec_2162506 Human_miRNA_ID_2794012,Human_miRNA_ID_2794013 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_269319 90214 RMVar_ID_90214 Human_SNP_ID_703157478 m1A Human chr22 - 36292176 36292176 36292176 GGACAGTGTGGGGTGCCTGGAAACTGCTGAGGAGGTGAAGAGGAAGCTCCAGAAGGACCTGGAGG GGACAGTGTGGGGTGCCTGGAAACTGCTGAGGGGGTGAAGAGGAAGCTCCAGAAGGACCTGGAGG T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36291904..36292297 26863196 MeRIP-seq:(Medium) rs750534869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65257,Human_RBP_ID_211780,Human_RBP_ID_4695023,Human_RBP_ID_8549459,Human_RBP_ID_8863330,Human_RBP_ID_9300690,Human_RBP_ID_9333352,Human_RBP_ID_9392273,Human_RBP_ID_18194340,Human_RBP_ID_18413186,Human_RBP_ID_21896549,Human_RBP_ID_22086526,Human_RBP_ID_22723956,Human_RBP_ID_24547083,Human_RBP_ID_26344918 Human_Splice_Rec_2162506 Human_miRNA_ID_2017412,Human_miRNA_ID_2017413,Human_miRNA_ID_2794012,Human_miRNA_ID_2794013 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_269319 90215 RMVar_ID_90215 Human_SNP_ID_703157818 m1A Human chr22 - 36293375 36293372 36293375 TTCCTTCCGGGAGCAGCTGGAGGAGGAGGAGGAGGCCAAGCACAACCTGGAGAAGCAGATCGCCA TTCCTTCCGGGAGCAGCTGGAGGAGGAGGAGG___CCAAGCACAACCTGGAGAAGCAGATCGCCA GCCT G MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:36293351..36293450 26863196 MeRIP-seq:(Medium) rs768181629 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_65258,Human_RBP_ID_152115,Human_RBP_ID_833705,Human_RBP_ID_5529922,Human_RBP_ID_8865717,Human_RBP_ID_9392275,Human_RBP_ID_17515020,Human_RBP_ID_17985575,Human_RBP_ID_22725446,Human_RBP_ID_26345372,Human_RBP_ID_27821273 Human_Splice_Rec_2162505 Human_miRNA_ID_2237934 RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_269319,RMVar_hsa_circ_117583,RMVar_hsa_circ_344803,RMVar_hsa_circ_214075 90216 RMVar_ID_90216 Human_SNP_ID_703158584 m1A Human chr22 + 36295715 36295715 36295715 GGGCCATGTTCTTCTGGGCAGCTTCCTCTTCCACTCTGCCAAAGCGACCAGCAACATCAGTATAA GGGCCATGTTCTTCTGGGCAGCTTCCTCTTCCCCTCTGCCAAAGCGACCAGCAACATCAGTATAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36295676..36295725 26863196 MeRIP-seq:(Medium) rs1314994311 Functional Loss SNV dbSNP153 33..33 33 - - - 90217 RMVar_ID_90217 Human_SNP_ID_703158585 m1A Human chr22 + 36295715 36295715 36295715 GGGCCATGTTCTTCTGGGCAGCTTCCTCTTCCACTCTGCCAAAGCGACCAGCAACATCAGTATAA GGGCCATGTTCTTCTGGGCAGCTTCCTCTTCCGCTCTGCCAAAGCGACCAGCAACATCAGTATAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36295676..36295725 26863196 MeRIP-seq:(Medium) rs1314994311 Functional Loss SNV dbSNP153 33..33 33 - - - 90218 RMVar_ID_90218 Human_SNP_ID_703158849 m1A Human chr22 + 36296794 36296794 36296794 GTGCCGAGAACTAGGGCCAGCAGCAAGCAGGAAGGGCTGGCCCAGGCCACCTGGCCTCAGGCGGG GTGCCGAGAACTAGGGCCAGCAGCAAGCAGGAGGGGCTGGCCCAGGCCACCTGGCCTCAGGCGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36296792..36296944 26863196 MeRIP-seq:(Medium) rs1421893169 Functional Loss SNV dbSNP153 33..33 33 - - - 90219 RMVar_ID_90219 Human_SNP_ID_703158857 m1A Human chr22 + 36296805 36296805 36296805 TAGGGCCAGCAGCAAGCAGGAAGGGCTGGCCCAGGCCACCTGGCCTCAGGCGGGCAGGCGGGGTC TAGGGCCAGCAGCAAGCAGGAAGGGCTGGCCCGGGCCACCTGGCCTCAGGCGGGCAGGCGGGGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:36296802..36297050;chr22:36296801..36296964 26863196 MeRIP-seq:(Medium) rs1305200711 Functional Loss SNV dbSNP153 33..33 33 - - - 90220 RMVar_ID_90220 Human_SNP_ID_703159975 m1A Human chr22 - 36300807 36300807 36300807 CTGCACCCGGGGAGGGGTGGCGCCGGAGGGGCAGGGCGGGGCGGAGGAGCAGGAACCAGGAGCTG CTGCACCCGGGGAGGGGTGGCGCCGGAGGGGCGGGGCGGGGCGGAGGAGCAGGAACCAGGAGCTG T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36300801..36301091 26863196 MeRIP-seq:(Medium) rs749682876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5389179,Human_RBP_ID_19113219,Human_RBP_ID_22362505,Human_RBP_ID_26789753 RMVar_hsa_circ_91840,RMVar_hsa_circ_122213,RMVar_hsa_circ_107935,RMVar_hsa_circ_214048,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_109659,RMVar_hsa_circ_117583,RMVar_hsa_circ_214075,RMVar_hsa_circ_41876,RMVar_hsa_circ_89,RMVar_hsa_circ_96166,RMVar_hsa_circ_104640,RMVar_hsa_circ_214076,RMVar_hsa_circ_214078,RMVar_hsa_circ_73354,RMVar_hsa_circ_214079,RMVar_hsa_circ_36127,RMVar_hsa_circ_1430,RMVar_hsa_circ_25411,RMVar_hsa_circ_93690,RMVar_hsa_circ_214080 90221 RMVar_ID_90221 Human_SNP_ID_703160500 m1A Human chr22 - 36302531 36302519 36302532 GTGCTAGAAGGGCCTCCTGAGTAGCTGGGACTACGGGTGCACACCACCATACATACCTGGCTAAT GTGCTAGAAGGGCCTCCTGAGTAGCTGGGAC_____________CACCATACATACCTGGCTAAT GGTGTGCACCCGTA G MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36302528..36302624 26863196 MeRIP-seq:(Medium) rs1156841759 Functional Loss DEL dbSNP153 32..44 33 - - - Human_RBP_ID_19111984 RMVar_hsa_circ_91840,RMVar_hsa_circ_107935,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_214067,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_109659,RMVar_hsa_circ_117583,RMVar_hsa_circ_214075,RMVar_hsa_circ_41876,RMVar_hsa_circ_12807,RMVar_hsa_circ_89,RMVar_hsa_circ_214076,RMVar_hsa_circ_1430,RMVar_hsa_circ_25411,RMVar_hsa_circ_93690,RMVar_hsa_circ_214080,RMVar_hsa_circ_90547,RMVar_hsa_circ_214081 90222 RMVar_ID_90222 Human_SNP_ID_703165723 m1A Human chr22 - 36320273 36320273 36320273 CATCCCCGGGCAGCAGGACAAGGACATGTTCCAGGAGACCATGGAGGCCATGAGGATTATGGGCA CATCCCCGGGCAGCAGGACAAGGACATGTTCCGGGAGACCATGGAGGCCATGAGGATTATGGGCA T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36320190..36320272 26863196 MeRIP-seq:(Medium) rs1334470148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65288,Human_RBP_ID_930275,Human_RBP_ID_1942431,Human_RBP_ID_5599406,Human_RBP_ID_7079624,Human_RBP_ID_8865736,Human_RBP_ID_17985588,Human_RBP_ID_26345389,Human_RBP_ID_26823124,Human_RBP_ID_27307327 Human_Splice_Rec_2162462,Human_Splice_Rec_2162463,Human_Splice_Rec_2162554,Human_Splice_Rec_2162566 RMVar_hsa_circ_13348,RMVar_hsa_circ_41876,RMVar_hsa_circ_20035,RMVar_hsa_circ_114176,RMVar_hsa_circ_47568,RMVar_hsa_circ_50362,RMVar_hsa_circ_80781,RMVar_hsa_circ_214087,RMVar_hsa_circ_13182,RMVar_hsa_circ_62653,RMVar_hsa_circ_214091,RMVar_hsa_circ_214089,RMVar_hsa_circ_105269,RMVar_hsa_circ_112325,RMVar_hsa_circ_88954,RMVar_hsa_circ_214094,RMVar_hsa_circ_50291,RMVar_hsa_circ_119857,RMVar_hsa_circ_122475,RMVar_hsa_circ_214095,RMVar_hsa_circ_214096,RMVar_hsa_circ_214097 90223 RMVar_ID_90223 Human_SNP_ID_703176837 m1A Human chr22 + 36362888 36362888 36362888 ATCACCCCAGAATGATAGCCCGCCCAGCATGGATAGAAGTGTGCCCCCTACAGCCTTTATAACCC ATCACCCCAGAATGATAGCCCGCCCAGCATGGGTAGAAGTGTGCCCCCTACAGCCTTTATAACCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36362886..36362982 26863196 MeRIP-seq:(Medium) rs1471603042 Functional Loss SNV dbSNP153 33..33 33 - - - 90224 RMVar_ID_90224 Human_SNP_ID_703182774 m1A Human chr22 + 36385827 36385827 36385827 GTGGCTCTCAAATTACACTGAGCAATCTCTCCATGTTTTTAATTACCCCCCAATTATCCACTAAG GTGGCTCTCAAATTACACTGAGCAATCTCTCCGTGTTTTTAATTACCCCCCAATTATCCACTAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36385824..36386006 26863196 MeRIP-seq:(Medium) rs1164149076 Functional Loss SNV dbSNP153 33..33 33 - - - 90225 RMVar_ID_90225 Human_SNP_ID_703201145 m1A Human chr22 - 36454854 36454854 36454854 GGAATCAGCCTTCCTCCAGGACGGCGCAGCCCACCGGGCGCCTGCTAAGTGCCCAGCACTGACCT GGAATCAGCCTTCCTCCAGGACGGCGCAGCCCTCCGGGCGCCTGCTAAGTGCCCAGCACTGACCT T A AL022313.2 Ensembl:ENSG00000228719 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36454847..36455044 26863196 MeRIP-seq:(Medium) rs1166972479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2162585 Human_miRNA_ID_3181003,Human_miRNA_ID_3181199,Human_miRNA_ID_3201596,Human_miRNA_ID_3207906 90226 RMVar_ID_90226 Human_SNP_ID_703201184 m1A Human chr22 - 36454953 36454953 36454953 GGAACAAGCCGGGGAGGGCTTGTTCGGCCACAAAGTTGGTTGCCGGGGTGGGGAGAATGTGCTGG GGAACAAGCCGGGGAGGGCTTGTTCGGCCACATAGTTGGTTGCCGGGGTGGGGAGAATGTGCTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36454902..36455029 26863196 MeRIP-seq:(Medium) rs930145650 Functional Loss SNV dbSNP153 33..33 33 - - - 90227 RMVar_ID_90227 Human_SNP_ID_703201185 m1A Human chr22 - 36454953 36454953 36454953 GGAACAAGCCGGGGAGGGCTTGTTCGGCCACAAAGTTGGTTGCCGGGGTGGGGAGAATGTGCTGG GGAACAAGCCGGGGAGGGCTTGTTCGGCCACAGAGTTGGTTGCCGGGGTGGGGAGAATGTGCTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36454902..36455029 26863196 MeRIP-seq:(Medium) rs930145650 Functional Loss SNV dbSNP153 33..33 33 - - - 90228 RMVar_ID_90228 Human_SNP_ID_703204660 m1A Human chr22 + 36467836 36467836 36467836 TCAGCCAATCAGCTTCTTCAGGAAGGCCTCCAACTGATCCTCATCCTTGATGCCCACAAACTTGT TCAGCCAATCAGCTTCTTCAGGAAGGCCTCCAGCTGATCCTCATCCTTGATGCCCACAAACTTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36467769..36467836 26863196 MeRIP-seq:(Medium) rs368164379 Functional Loss SNV dbSNP153 33..33 33 - - - 90229 RMVar_ID_90229 Human_SNP_ID_703208333 m1A Human chr22 + 36481461 36481442 36481461 CGGACATCACCAGGGACCCTGGCTCTCCGGCGAGCTAGATCCCCCCGCCCGCCCGGCCGCCAGCC CGGACATCACCAGG___________________GCTAGATCCCCCCGCCCGCCCGGCCGCCAGCC GGACCCTGGCTCTCCGGCGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36481454..36481579 26863196 MeRIP-seq:(Medium) rs1246000096 Functional Loss DEL dbSNP153 15..33 33 - - - 90230 RMVar_ID_90230 Human_SNP_ID_703209503 m1A Human chr22 - 36485056 36485056 36485056 AGGAAGAGAGAGGCAGAGAGAGAGGCAAAGAGAAAGAGTGAGAGAGAAAAAGAGGCAGAGAGGGA AGGAAGAGAGAGGCAGAGAGAGAGGCAAAGAGGAAGAGTGAGAGAGAAAAAGAGGCAGAGAGGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36485032..36485174 26863196 MeRIP-seq:(Medium) rs1245677589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25668272 90231 RMVar_ID_90231 Human_SNP_ID_703210413 m1A Human chr22 - 36488233 36488233 36488233 CCCCATCTCAAAAAAATAAAAAATAAAAAAGAACAAAGTATGCTACAACAAAAGTGAAAAGAGAA CCCCATCTCAAAAAAATAAAAAATAAAAAAGATCAAAGTATGCTACAACAAAAGTGAAAAGAGAA T A FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:36488207..36488292 26863196 MeRIP-seq:(Medium) rs1054955468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579273,Human_RBP_ID_23012866 Human_miRNA_ID_1133561 90232 RMVar_ID_90232 Human_SNP_ID_703215163 m1A Human chr22 - 36506085 36506085 36506085 GCTCAGCCACGACCCCCGGCTGCTCTTCAGACACTACTCGCGTGCCTACTTCCCCGACGCCCGCG GCTCAGCCACGACCCCCGGCTGCTCTTCAGACTCTACTCGCGTGCCTACTTCCCCGACGCCCGCG T A FOXRED2 Ensembl:ENSG00000100350 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36505976..36506200 26863196 MeRIP-seq:(Medium) rs753652767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8863412,Human_RBP_ID_22768296,Human_RBP_ID_27036569,Human_RBP_ID_27307421,Human_RBP_ID_27493592 RMVar_hsa_circ_30127 90233 RMVar_ID_90233 Human_SNP_ID_703215164 m1A Human chr22 - 36506085 36506085 36506085 GCTCAGCCACGACCCCCGGCTGCTCTTCAGACACTACTCGCGTGCCTACTTCCCCGACGCCCGCG GCTCAGCCACGACCCCCGGCTGCTCTTCAGACCCTACTCGCGTGCCTACTTCCCCGACGCCCGCG T G FOXRED2 Ensembl:ENSG00000100350 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:36505976..36506200 26863196 MeRIP-seq:(Medium) rs753652767 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8863412,Human_RBP_ID_22768296,Human_RBP_ID_27036569,Human_RBP_ID_27307421,Human_RBP_ID_27493592 RMVar_hsa_circ_30127 90234 RMVar_ID_90234 Human_SNP_ID_703215167 m1A Human chr22 + 36506094 36506094 36506094 CGGGGAAGTAGGCACGCGAGTAGTGTCTGAAGAGCAGCCGGGGGTCGTGGCTGAGCAGAGAGTTC CGGGGAAGTAGGCACGCGAGTAGTGTCTGAAGGGCAGCCGGGGGTCGTGGCTGAGCAGAGAGTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36506049..36506162 26863196 MeRIP-seq:(Medium) rs1334968846 Functional Loss SNV dbSNP153 33..33 33 - - - 90235 RMVar_ID_90235 Human_SNP_ID_703215515 m1A Human chr22 + 36506939 36506939 36506939 CACACCTGCCGCCCGCCCGCGTGCGCTTCAGGAGCCGCCAGGTCCCTACGCCCGCAGCTCCGGCC CACACCTGCCGCCCGCCCGCGTGCGCTTCAGGGGCCGCCAGGTCCCTACGCCCGCAGCTCCGGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr22:36506686..36507003;chr22:36506834..36507015 26863196 MeRIP-seq:(Medium) rs987818009 Functional Loss SNV dbSNP153 33..33 33 - - - 90236 RMVar_ID_90236 Human_SNP_ID_703215535 m1A Human chr22 - 36506993 36506993 36506993 GCCGGAGCGGCTGGGAGGTTCGCGCGTTTCTCAGGGTTCGGTCGGAGGCGGGGAGGCCGGAGCTG GCCGGAGCGGCTGGGAGGTTCGCGCGTTTCTCGGGGTTCGGTCGGAGGCGGGGAGGCCGGAGCTG T C FOXRED2 Ensembl:ENSG00000100350 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36506611..36507050 26863196 MeRIP-seq:(Medium) rs1277153934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4695467,Human_RBP_ID_5504647,Human_RBP_ID_17069141,Human_RBP_ID_18423642 Human_Splice_Rec_2162633 90237 RMVar_ID_90237 Human_SNP_ID_703218307 m1A Human chr22 - 36516543 36516543 36516543 ACCTTATTGTCCGTTGTGAGCACGATGGCGTCATGACTGGAGCCAACGGGGAAGTGTCCTTCATC ACCTTATTGTCCGTTGTGAGCACGATGGCGTCGTGACTGGAGCCAACGGGGAAGTGTCCTTCATC T C EIF3D Ensembl:ENSG00000100353 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36516433..36516596 26863196 MeRIP-seq:(Medium) rs753557103 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_579360,Human_RBP_ID_781371,Human_RBP_ID_1610924,Human_RBP_ID_1942478,Human_RBP_ID_3672333,Human_RBP_ID_7079791,Human_RBP_ID_8863433,Human_RBP_ID_9260685,Human_RBP_ID_9300380,Human_RBP_ID_9392322,Human_RBP_ID_14475496,Human_RBP_ID_18194093,Human_RBP_ID_22454449,Human_RBP_ID_22820371,Human_RBP_ID_23946157,Human_RBP_ID_26344931 Human_Splice_Rec_2162692,Human_Splice_Rec_2162693,Human_Splice_Rec_2162726,Human_Splice_Rec_2162727,Human_Splice_Rec_2162734,Human_Splice_Rec_2162735,Human_Splice_Rec_2162746,Human_Splice_Rec_2162747,Human_Splice_Rec_2162752 RMVar_hsa_circ_25714,RMVar_hsa_circ_86827,RMVar_hsa_circ_214122,RMVar_hsa_circ_88800,RMVar_hsa_circ_122597,RMVar_hsa_circ_39104,RMVar_hsa_circ_214123,RMVar_hsa_circ_214124,RMVar_hsa_circ_120712,RMVar_hsa_circ_286190,RMVar_hsa_circ_214125,RMVar_hsa_circ_112237,RMVar_hsa_circ_214126 90238 RMVar_ID_90238 Human_SNP_ID_703218642 m1A Human chr22 - 36517778 36517778 36517778 ACACCACTGCACTCCAACCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAGTGTTTATAT ACACCACTGCACTCCAACCTGGGTGACAGAGCTAGACTCCATCTCAAAAAAAAAAGTGTTTATAT T A EIF3D Ensembl:ENSG00000100353 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1439743200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86827,RMVar_hsa_circ_122597,RMVar_hsa_circ_39104,RMVar_hsa_circ_214123,RMVar_hsa_circ_214124,RMVar_hsa_circ_120712,RMVar_hsa_circ_286190,RMVar_hsa_circ_214125,RMVar_hsa_circ_112237,RMVar_hsa_circ_91327,RMVar_hsa_circ_214126,RMVar_hsa_circ_214127 90239 RMVar_ID_90239 Human_SNP_ID_703218940 m1A Human chr22 - 36518897 36518895 36518897 TCTTTGATCCTCTTTGCAGCTGGCAAAAACTCAGGGGAATGTGTTTGCCACTGATGCCATCCTGG TCTTTGATCCTCTTTGCAGCTGGCAAAAACTC__GGGAATGTGTTTGCCACTGATGCCATCCTGG CCT C EIF3D Ensembl:ENSG00000100353 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36518728..36518952 26863196 MeRIP-seq:(Medium) rs1257255465 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4695516,Human_RBP_ID_18194094,Human_RBP_ID_20758165,Human_RBP_ID_23946183,Human_RBP_ID_26822471 Human_Splice_Rec_2162686,Human_Splice_Rec_2162720,Human_Splice_Rec_2162740,Human_Splice_Rec_2162770 Human_miRNA_ID_2614002,Human_miRNA_ID_2769465 RMVar_hsa_circ_86827,RMVar_hsa_circ_122597,RMVar_hsa_circ_39104,RMVar_hsa_circ_214123,RMVar_hsa_circ_214124,RMVar_hsa_circ_120712,RMVar_hsa_circ_286190,RMVar_hsa_circ_214125,RMVar_hsa_circ_112237,RMVar_hsa_circ_95196,RMVar_hsa_circ_300262,RMVar_hsa_circ_91327,RMVar_hsa_circ_214126,RMVar_hsa_circ_214127,RMVar_hsa_circ_325181,RMVar_hsa_circ_109028,RMVar_hsa_circ_276724,RMVar_hsa_circ_99211,RMVar_hsa_circ_214129,RMVar_hsa_circ_214131,RMVar_hsa_circ_30994,RMVar_hsa_circ_214130,RMVar_hsa_circ_214128 90240 RMVar_ID_90240 Human_SNP_ID_703220856 m1A Human chr22 - 36526002 36526002 36526002 TACCAGCCGTTCAGCAAAGGAGATCGGCTAGGAAAGGTACATGCCTGTCAGCAGGAGTCTGAATC TACCAGCCGTTCAGCAAAGGAGATCGGCTAGGGAAGGTACATGCCTGTCAGCAGGAGTCTGAATC T C EIF3D Ensembl:ENSG00000100353 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs772769396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781374,Human_RBP_ID_9392327,Human_RBP_ID_14475832,Human_RBP_ID_17985680,Human_RBP_ID_22454964,Human_RBP_ID_22675278,Human_RBP_ID_23258543 Human_Splice_Rec_2162673,Human_Splice_Rec_2162707,Human_Splice_Rec_2162757,Human_Splice_Rec_2162773,Human_Splice_Rec_2162785,Human_Splice_Rec_2162795 Human_miRNA_ID_2569753 RMVar_hsa_circ_10746,RMVar_hsa_circ_99211,RMVar_hsa_circ_214131,RMVar_hsa_circ_39329,RMVar_hsa_circ_340471 90241 RMVar_ID_90241 Human_SNP_ID_703284402 m1A Human chr22 - 36770642 36770642 36770642 GAGGTGACCCGTTGAATCTGGGGACGATGAAAACACACGGTGGCGTCACAAACAGAAAGCTTGGG GAGGTGACCCGTTGAATCTGGGGACGATGAAAGCACACGGTGGCGTCACAAACAGAAAGCTTGGG T C IFT27 Ensembl:ENSG00000100360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:36770636..36770792 26863196 MeRIP-seq:(Medium) rs1326737123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14476203 90242 RMVar_ID_90242 Human_SNP_ID_703284686 m1A Human chr22 - 36771802 36771802 36771802 ATGCCACCCACTGGGTGGATAACAGCCGGGAGAAAAAAGAAGAGAAAAGAAGTGTTCAAGGCACA ATGCCACCCACTGGGTGGATAACAGCCGGGAGGAAAAAGAAGAGAAAAGAAGTGTTCAAGGCACA T C IFT27 Ensembl:ENSG00000100360 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:36771800..36771884 26863196 MeRIP-seq:(Medium) rs937681265 Functional Loss SNV dbSNP153 33..33 33 - - - 90243 RMVar_ID_90243 Human_SNP_ID_703285660 m1A Human chr22 + 36775853 36775853 36775853 GGCTGATCTCAAGGGTCAGTGGCCGCGACGGGACTGGGGATGACCGAGCCCGGCCCTTCTGGGCC GGCTGATCTCAAGGGTCAGTGGCCGCGACGGGCCTGGGGATGACCGAGCCCGGCCCTTCTGGGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36775802..36776112 26863196 MeRIP-seq:(Medium) rs542596060 Functional Loss SNV dbSNP153 33..33 33 - - - 90244 RMVar_ID_90244 Human_SNP_ID_703285691 m1A Human chr22 + 36775925 36775925 36775925 GATATCGGGCGCTGGGGGCGGGTGGGCAGGGGAGGGCTCCAGGTGGGCCCGGCTCGAGGCCTGAC GATATCGGGCGCTGGGGGCGGGTGGGCAGGGGGGGGCTCCAGGTGGGCCCGGCTCGAGGCCTGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:36775878..36776009 32194978 MeRIP-seq:(Medium) rs921819475 Functional Loss SNV dbSNP153 33..33 33 - - - 90245 RMVar_ID_90245 Human_SNP_ID_703349059 m1A Human chr22 - 37011066 37011066 37011066 TCCTGGTCCGAGTGGTTTCGCCGGGCCCCCCCAGAGAGCCGTGTGTCCCAGGGAAAGTCTGAGAA TCCTGGTCCGAGTGGTTTCGCCGGGCCCCCCCCGAGAGCCGTGTGTCCCAGGGAAAGTCTGAGAA T G TST Ensembl:ENSG00000128311 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37011023..37011115 26863196 MeRIP-seq:(Medium) rs1361959230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579404,Human_RBP_ID_5119916 Human_miRNA_ID_2425908,Human_miRNA_ID_2435579 RMVar_hsa_circ_101935,RMVar_hsa_circ_115223,RMVar_hsa_circ_122567,RMVar_hsa_circ_105734,RMVar_hsa_circ_214138,RMVar_hsa_circ_214140,RMVar_hsa_circ_214141,RMVar_hsa_circ_214139 90246 RMVar_ID_90246 Human_SNP_ID_703351149 m1A Human chr22 - 37018513 37018513 37018513 AGTGCCGGGACACGGCGTCGCCCTACGAGATGATGCTGCCCAGCGAGGCTGGCTTCGCCGAGTAT AGTGCCGGGACACGGCGTCGCCCTACGAGATGTTGCTGCCCAGCGAGGCTGGCTTCGCCGAGTAT T A TST Ensembl:ENSG00000128311 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37018464..37018565 32194978 MeRIP-seq:(Medium) rs780500939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579411,Human_RBP_ID_8549624,Human_RBP_ID_9392903,Human_RBP_ID_22087353 Human_miRNA_ID_1938694,Human_miRNA_ID_1949794,Human_miRNA_ID_2398727 RMVar_hsa_circ_115223,RMVar_hsa_circ_122567,RMVar_hsa_circ_105734,RMVar_hsa_circ_214140,RMVar_hsa_circ_214141,RMVar_hsa_circ_214139 90247 RMVar_ID_90247 Human_SNP_ID_703351382 m1A Human chr22 - 37019279 37019279 37019279 GACGGGGTGCCCCGGGAACCCCTGATCCACCTAGGGCAGAGGGCAGCGAGCTACGGGCCGGACTC GACGGGGTGCCCCGGGAACCCCTGATCCACCTGGGGCAGAGGGCAGCGAGCTACGGGCCGGACTC T C TST Ensembl:ENSG00000128311 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37019265..37019410 26863196 MeRIP-seq:(Medium) rs1006820605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833772,Human_RBP_ID_932244,Human_RBP_ID_18423741,Human_RBP_ID_18464187,Human_RBP_ID_22725126,Human_RBP_ID_26789758 RMVar_hsa_circ_122567,RMVar_hsa_circ_105734,RMVar_hsa_circ_214140,RMVar_hsa_circ_214141 90248 RMVar_ID_90248 Human_SNP_ID_703351579 m1A Human chr22 + 37019795 37019795 37019795 GGTCCGCTGCAGGTTGGTGGCGGGAGGAGGGGACAGCTGCGGGCGCGGGGAGGGGGCGCCGCGCC GGTCCGCTGCAGGTTGGTGGCGGGAGGAGGGGGCAGCTGCGGGCGCGGGGAGGGGGCGCCGCGCC A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37019789..37019928 26863196 MeRIP-seq:(Medium) rs1404929964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4695677,Human_RBP_ID_9432881 Human_Splice_Rec_2163197,Human_Splice_Rec_2163203,Human_Splice_Rec_2163213 90249 RMVar_ID_90249 Human_SNP_ID_703351601 m1A Human chr22 - 37019838 37019838 37019838 GGGTCTCGGACTCCCGGCTTCCTGGCTCCGCCATGGCCCCCGCGGCGCGGCGCCCCCTCCCCGCG GGGTCTCGGACTCCCGGCTTCCTGGCTCCGCCGTGGCCCCCGCGGCGCGGCGCCCCCTCCCCGCG T C TST Ensembl:ENSG00000128311 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:37019776..37020148;chr22:37019733..37023097 26863196 MeRIP-seq:(Medium) rs1357880566 Functional Loss SNV dbSNP153 33..33 33 - - - 90250 RMVar_ID_90250 Human_SNP_ID_703351677 m1A Human chr22 - 37020087 37020087 37020087 CCCTCTCTGGTGCCACCAGGTCACCCACTTCCACCCAAGGCTCCCCACCCGCCACTCGCCACGAC CCCTCTCTGGTGCCACCAGGTCACCCACTTCCCCCCAAGGCTCCCCACCCGCCACTCGCCACGAC T G TST Ensembl:ENSG00000128311 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:37019859..37020096 26863196 MeRIP-seq:(Medium) rs1012118782 Functional Loss SNV dbSNP153 33..33 33 - - - 90251 RMVar_ID_90251 Human_SNP_ID_703352803 m1A Human chr22 + 37024502 37024502 37024502 CGCAGGCCGCCTGGGCGTGGGCGCGGCCACCCACGTCGTGATCTACGACGCCAGCGACCAGGGCC CGCAGGCCGCCTGGGCGTGGGCGCGGCCACCCCCGTCGTGATCTACGACGCCAGCGACCAGGGCC A C MPST Ensembl:ENSG00000128309 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37024451..37024550 26863196 MeRIP-seq:(Medium) rs767918500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833715,Human_RBP_ID_9332826,Human_RBP_ID_17985699,Human_RBP_ID_18194098,Human_RBP_ID_22086535 RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 90252 RMVar_ID_90252 Human_SNP_ID_703352804 m1A Human chr22 + 37024502 37024502 37024502 CGCAGGCCGCCTGGGCGTGGGCGCGGCCACCCACGTCGTGATCTACGACGCCAGCGACCAGGGCC CGCAGGCCGCCTGGGCGTGGGCGCGGCCACCCGCGTCGTGATCTACGACGCCAGCGACCAGGGCC A G MPST Ensembl:ENSG00000128309 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37024451..37024550 26863196 MeRIP-seq:(Medium) rs767918500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833715,Human_RBP_ID_9332826,Human_RBP_ID_17985699,Human_RBP_ID_18194098,Human_RBP_ID_22086535 RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 90253 RMVar_ID_90253 Human_SNP_ID_703352823 m1A Human chr22 - 37024540 37024540 37024540 GGCGCGGAACATCCACCAGACGCGCGGGGCGGAGTAGAGGCCCTGGTCGCTGGCGTCGTAGATCA GGCGCGGAACATCCACCAGACGCGCGGGGCGGGGTAGAGGCCCTGGTCGCTGGCGTCGTAGATCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37024526..37024550 32194978 MeRIP-seq:(Medium) rs1192844149 Functional Loss SNV dbSNP153 33..33 33 - - - 90254 RMVar_ID_90254 Human_SNP_ID_703352856 m1A Human chr22 - 37024595 37024595 37024595 GGCGCAGCCAGTGGCGGAGGCCGCCATCAAGCAGTGACACGGCGTGGTGGCCGAAGGCGCGGAAC GGCGCAGCCAGTGGCGGAGGCCGCCATCAAGCTGTGACACGGCGTGGTGGCCGAAGGCGCGGAAC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37024514..37024839 26863196 MeRIP-seq:(Medium) rs773526827 Functional Loss SNV dbSNP153 33..33 33 - - - 90255 RMVar_ID_90255 Human_SNP_ID_703352928 m1A Human chr22 + 37024705 37024705 37024705 AGTTCCGCGCTCAGCTCGACCCCGCCTTCATCAAGACCTACGAGGACATCAAGGAGAACCTGGAA AGTTCCGCGCTCAGCTCGACCCCGCCTTCATCGAGACCTACGAGGACATCAAGGAGAACCTGGAA A G MPST Ensembl:ENSG00000128309 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:37024606..37024807 26863196 MeRIP-seq:(Medium) rs1330850254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579422,Human_RBP_ID_5599409,Human_RBP_ID_17985700,Human_RBP_ID_18194357,Human_RBP_ID_27307504 RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 90256 RMVar_ID_90256 Human_SNP_ID_703354056 m1A Human chr22 - 37029193 37029193 37029193 GGTTCAATGCCTACAGCAGGGGAGCAGGGAGGAGGGGACAAATAGAAGGATGCTATGAATGGTAC GGTTCAATGCCTACAGCAGGGGAGCAGGGAGGGGGGGACAAATAGAAGGATGCTATGAATGGTAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37029190..37029314 26863196 MeRIP-seq:(Medium) rs1334833860 Functional Loss SNV dbSNP153 33..33 33 - - - 90257 RMVar_ID_90257 Human_SNP_ID_703359761 m1A Human chr22 + 37051817 37051792 37051817 GCGCCGCCGGCGGGGGCGGGCGGCCGCGCCGCAGGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT GCGCCGCC_________________________GGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT CGGCGGGGGCGGGCGGCCGCGCCGCA C KCTD17 Ensembl:ENSG00000100379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37051770..37051895 26863196 MeRIP-seq:(Medium) rs1268686731 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_834195,Human_RBP_ID_4695755 RMVar_hsa_circ_75566,RMVar_hsa_circ_214143 90258 RMVar_ID_90258 Human_SNP_ID_703359776 m1A Human chr22 + 37051817 37051817 37051817 GCGCCGCCGGCGGGGGCGGGCGGCCGCGCCGCAGGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT GCGCCGCCGGCGGGGGCGGGCGGCCGCGCCGCCGGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT A C KCTD17 Ensembl:ENSG00000100379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37051770..37051895 26863196 MeRIP-seq:(Medium) rs1203578535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834195,Human_RBP_ID_4695755 RMVar_hsa_circ_75566,RMVar_hsa_circ_214143 90259 RMVar_ID_90259 Human_SNP_ID_703359777 m1A Human chr22 + 37051817 37051817 37051817 GCGCCGCCGGCGGGGGCGGGCGGCCGCGCCGCAGGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT GCGCCGCCGGCGGGGGCGGGCGGCCGCGCCGCGGGCGGCTGGGGCAAGTGGGTGCGGCTCAACGT A G KCTD17 Ensembl:ENSG00000100379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37051770..37051895 26863196 MeRIP-seq:(Medium) rs1203578535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834195,Human_RBP_ID_4695755 RMVar_hsa_circ_75566,RMVar_hsa_circ_214143 90260 RMVar_ID_90260 Human_SNP_ID_703362362 m1A Human chr22 - 37061258 37061258 37061258 CCGGGATGGAGGCGTGAGCAGGCAGAGAGAAAACCCGGACAGGGGCAGAGAGGGAAGAGGCAGGG CCGGGATGGAGGCGTGAGCAGGCAGAGAGAAAGCCCGGACAGGGGCAGAGAGGGAAGAGGCAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37061222..37061324 26863196 MeRIP-seq:(Medium) rs1040718308 Functional Loss SNV dbSNP153 33..33 33 - - - 90261 RMVar_ID_90261 Human_SNP_ID_703395479 m1A Human chr22 - 37180719 37180719 37180719 CGTTTCCCCAGGGCCTCCAGCTGCCCTCAGACACTGATGTCTGTCCCCAGGTGCTCTCTGCCCCT CGTTTCCCCAGGGCCTCCAGCTGCCCTCAGACGCTGATGTCTGTCCCCAGGTGCTCTCTGCCCCT T C C1QTNF6 Ensembl:ENSG00000133466 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37180668..37180922 26863196 MeRIP-seq:(Medium) rs368232130 Functional Loss SNV dbSNP153 33..33 33 - - - 90262 RMVar_ID_90262 Human_SNP_ID_703395832 m1A Human chr22 + 37182139 37182139 37182139 TTCACAGCAGTGCAAACTGAGCCCTGCAGGGGACGGGACCAGCACCTGAGCTCTCCAGCCGGGAG TTCACAGCAGTGCAAACTGAGCCCTGCAGGGGGCGGGACCAGCACCTGAGCTCTCCAGCCGGGAG A G Z82188.2 Ensembl:ENSG00000235237 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37182091..37182288 26863196 MeRIP-seq:(Medium) rs1342202307 Functional Loss SNV dbSNP153 33..33 33 - - - 90263 RMVar_ID_90263 Human_SNP_ID_703397577 m1A Human chr22 + 37187936 37187936 37187936 GGGCAACTTTTCTCGGTCCAGGCAGGCCGTGCAGAGCTGAGTTTGTGTGTGCCCGGGTAGGGGCG GGGCAACTTTTCTCGGTCCAGGCAGGCCGTGCCGAGCTGAGTTTGTGTGTGCCCGGGTAGGGGCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37187933..37188044 26863196 MeRIP-seq:(Medium) rs1361237285 Functional Loss SNV dbSNP153 33..33 33 - - - 90264 RMVar_ID_90264 Human_SNP_ID_703397664 m1A Human chr22 - 37188213 37188213 37188213 TATTGCAGACATGGGCCAAGGAGCCAGAGGCCATGCAGTGGCTCAGGGTCCGTGAGTCGCCTGGG TATTGCAGACATGGGCCAAGGAGCCAGAGGCCTTGCAGTGGCTCAGGGTCCGTGAGTCGCCTGGG T A C1QTNF6 Ensembl:ENSG00000133466 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:37188104..37188278;chr22:37188101..37188216;chr22:37188092..37188261 26863196 MeRIP-seq:(Medium) rs942158423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2163541,Human_Splice_Rec_2163545,Human_Splice_Rec_2163557,Human_Splice_Rec_2163569 90265 RMVar_ID_90265 Human_SNP_ID_703399999 m1A Human chr22 + 37198110 37198110 37198110 GACAACAGCATGACCAGGAGGAGCGCAGGCCCAGGGTGGCTCTCATCACCCTGCTATCACTCCCA GACAACAGCATGACCAGGAGGAGCGCAGGCCCGGGGTGGCTCTCATCACCCTGCTATCACTCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37198059..37198274 26863196 MeRIP-seq:(Medium) rs745804221 Functional Loss SNV dbSNP153 33..33 33 - - - 90266 RMVar_ID_90266 Human_SNP_ID_703407460 m1A Human chr22 - 37225753 37225753 37225753 AAGCCACCCCCGTGTTCCTGCCGTCAGTGCCAACTGCCGCATGTGGAAGCATCTACCCGTTCACT AAGCCACCCCCGTGTTCCTGCCGTCAGTGCCAGCTGCCGCATGTGGAAGCATCTACCCGTTCACT T C RAC2 Ensembl:ENSG00000128340 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37225703..37225782 26863196 MeRIP-seq:(Medium) rs913835427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152251,Human_RBP_ID_1101908,Human_RBP_ID_3679563,Human_RBP_ID_17399808,Human_RBP_ID_17516042,Human_RBP_ID_17573293,Human_RBP_ID_26500985 Human_miRNA_ID_140123,Human_miRNA_ID_417080,Human_miRNA_ID_1013095,Human_miRNA_ID_1021253,Human_miRNA_ID_1295098,Human_miRNA_ID_1299060,Human_miRNA_ID_1821445,Human_miRNA_ID_1912819,Human_miRNA_ID_1987303,Human_miRNA_ID_3123823 RMVar_hsa_circ_103166,RMVar_hsa_circ_214149 90267 RMVar_ID_90267 Human_SNP_ID_703444230 m1A Human chr22 + 37368636 37368636 37368636 CAGCCACCTCTGGAGCAGCCACCTTGTCAGACAGGAGAGGTGGCAATGGGGCCAGCCAGGCAAGG CAGCCACCTCTGGAGCAGCCACCTTGTCAGACTGGAGAGGTGGCAATGGGGCCAGCCAGGCAAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37368587..37368712 32194978 MeRIP-seq:(Medium) rs1016609182 Functional Loss SNV dbSNP153 33..33 33 - - - 90268 RMVar_ID_90268 Human_SNP_ID_703444254 m1A Human chr22 + 37368703 37368703 37368703 GCCCTAACCTTCACACTGGCTTCCACGGGCAAAGTAAGCCCCTCAGGGCTGAGCTTCCCCAGGCT GCCCTAACCTTCACACTGGCTTCCACGGGCAAGGTAAGCCCCTCAGGGCTGAGCTTCCCCAGGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37368691..37368824 26863196 MeRIP-seq:(Medium) rs1314252754 Functional Loss SNV dbSNP153 33..33 33 - - - 90269 RMVar_ID_90269 Human_SNP_ID_703446497 m1A Human chr22 - 37375705 37375705 37375705 CTAGCCAGGCCTAGTGCCTGCTGTAGCACCCTAGAAGATCCCCAGCAGTTGGCACTAGCTGTACC CTAGCCAGGCCTAGTGCCTGCTGTAGCACCCTGGAAGATCCCCAGCAGTTGGCACTAGCTGTACC T C FP325335.1,ELFN2 Ensembl:ENSG00000243902,Ensembl:ENSG00000166897 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37375700..37375834 26863196 MeRIP-seq:(Medium) rs1421030033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214151 90270 RMVar_ID_90270 Human_SNP_ID_703449983 m1A Human chr22 - 37388610 37388610 37388610 CTGAGATCTGTGCAAAAGCTGACCCCTCCCCGACTTCCCCAGGGAGCAGAAGAGCCCAGAAGAGC CTGAGATCTGTGCAAAAGCTGACCCCTCCCCGTCTTCCCCAGGGAGCAGAAGAGCCCAGAAGAGC T A FP325335.1,ELFN2 Ensembl:ENSG00000243902,Ensembl:ENSG00000166897 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37387607..37388741 26863196 MeRIP-seq:(Medium) rs928010378 Functional Loss SNV dbSNP153 33..33 33 - - - 90271 RMVar_ID_90271 Human_SNP_ID_703450201 m1A Human chr22 + 37389667 37389667 37389667 GAGGAACAGCAGCTCTCCAGTGATGCACTTGAACCCGGGTCTCTGCTGCATCCAGCCCACCAAGC GAGGAACAGCAGCTCTCCAGTGATGCACTTGAGCCCGGGTCTCTGCTGCATCCAGCCCACCAAGC A G lnc-CYTH4-5 RNACentral:URS00008BD416 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37389661..37389882 26863196 MeRIP-seq:(Medium) rs1313722997 Functional Loss SNV dbSNP153 33..33 33 - - - 90272 RMVar_ID_90272 Human_SNP_ID_703460012 m1A Human chr22 - 37427453 37427453 37427453 GGCGGCGTCTGCGCGCACACGCGCGCTCCCAGACACACACACAGACACACGCGGGCCACCCCACG GGCGGCGTCTGCGCGCACACGCGCGCTCCCAGGCACACACACAGACACACGCGGGCCACCCCACG T C ELFN2 Ensembl:ENSG00000166897 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37427088..37427637 26863196 MeRIP-seq:(Medium) rs895540440 Functional Loss SNV dbSNP153 33..33 33 - - - 90273 RMVar_ID_90273 Human_SNP_ID_703470434 m1A Human chr22 + 37470991 37470991 37470991 TAGCGAACTCCTGCTAGCCCTTCAGGTCCTTCACGTTACCTCCTCACAGAAGCCTTCCCCGGCCA TAGCGAACTCCTGCTAGCCCTTCAGGTCCTTCGCGTTACCTCCTCACAGAAGCCTTCCCCGGCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37470808..37471201 26863196 MeRIP-seq:(Medium) rs138424778 Functional Loss SNV dbSNP153 33..33 33 - - - 90274 RMVar_ID_90274 Human_SNP_ID_703475327 m1A Human chr22 - 37489605 37489591 37489605 GAGGCTGTGGGAGCCTCTCAGGATGTGGGAGCAGGGCTATGGGAGCTCTGGTTTGGAGTTGACTT GAGGCTGTGGGAGCCTCTCAGGATGTGGGAGC______________TCTGGTTTGGAGTTGACTT AGCTCCCATAGCCCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37489556..37489750 26863196 MeRIP-seq:(Medium) rs1334791211 Functional Loss DEL dbSNP153 33..46 33 - - - 90275 RMVar_ID_90275 Human_SNP_ID_703480562 m1A Human chr22 - 37508137 37508137 37508137 AAATGATGATCATTCTTCTCGTTTTACAGATTAGGCAGTTGAGGGCCTGTGAGGTAAAGTCAGTG AAATGATGATCATTCTTCTCGTTTTACAGATTGGGCAGTTGAGGGCCTGTGAGGTAAAGTCAGTG T C CARD10 Ensembl:ENSG00000100065 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37508133..37508320 26863196 MeRIP-seq:(Medium) rs1569165944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1068789,Human_RBP_ID_5388265,Human_RBP_ID_22418154,Human_RBP_ID_25668706 RMVar_hsa_circ_63324,RMVar_hsa_circ_110294,RMVar_hsa_circ_214159,RMVar_hsa_circ_68636,RMVar_hsa_circ_79700,RMVar_hsa_circ_214161 90276 RMVar_ID_90276 Human_SNP_ID_703481465 m1A Human chr22 - 37510358 37510358 37510358 TGGAGGAAGAGTGTGCACTGCTTCGAAGGGCCAGGGGCCCGCCCCCTGGGGCAGAGGAGAAGGAG TGGAGGAAGAGTGTGCACTGCTTCGAAGGGCCTGGGGCCCGCCCCCTGGGGCAGAGGAGAAGGAG T A CARD10 Ensembl:ENSG00000100065 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:37510048..37510452;chr22:37510061..37510462 26863196 MeRIP-seq:(Medium) rs771698026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708188 Human_Splice_Rec_2163902,Human_Splice_Rec_2163942,Human_Splice_Rec_2164016,Human_Splice_Rec_2164062 RMVar_hsa_circ_63324,RMVar_hsa_circ_110294,RMVar_hsa_circ_214159,RMVar_hsa_circ_68636,RMVar_hsa_circ_79700,RMVar_hsa_circ_214161 90277 RMVar_ID_90277 Human_SNP_ID_703484028 m1A Human chr22 - 37519217 37519217 37519217 CTGGTCGACCCCCGTGCGCCTCTTGCCCGCAGACCCTGAGGACACGGCCATGCCGGGCCGGGCGG CTGGTCGACCCCCGTGCGCCTCTTGCCCGCAGGCCCTGAGGACACGGCCATGCCGGGCCGGGCGG T C CARD10 Ensembl:ENSG00000100065 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37519173..37519500 26863196 MeRIP-seq:(Medium) rs764095805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709002 Human_Splice_Rec_2163936 RMVar_hsa_circ_63324,RMVar_hsa_circ_110294,RMVar_hsa_circ_214159,RMVar_hsa_circ_79700,RMVar_hsa_circ_214161 90278 RMVar_ID_90278 Human_SNP_ID_703495085 m1A Human chr22 + 37560542 37560540 37560543 CCAGCCGGGACGCGCGGCCGCCGCCGCTGCAGACGACGAGTCCGCCCTCGTCCCGCGCCCCCGGG CCAGCCGGGACGCGCGGCCGCCGCCGCTGCA___GACGAGTCCGCCCTCGTCCCGCGCCCCCGGG AGAC A CDC42EP1 Ensembl:ENSG00000128283 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:37560451..37560970;chr22:37560476..37560924 26863196 MeRIP-seq:(Medium) rs1430699686 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10685,Human_RBP_ID_4695849 Human_Splice_Rec_2164067,Human_Splice_Rec_2164071 RMVar_hsa_circ_79438,RMVar_hsa_circ_214164 90279 RMVar_ID_90279 Human_SNP_ID_703496697 m1A Human chr22 - 37566119 37566119 37566119 TCAGAAGCAGCTATAGATGTTCAAGCGCAGAGAAAGCACCCCCGAGGTGGTCGGCAACTCTCCTG TCAGAAGCAGCTATAGATGTTCAAGCGCAGAGTAAGCACCCCCGAGGTGGTCGGCAACTCTCCTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37566076..37566175 26863196 MeRIP-seq:(Medium) rs138215550 Functional Loss SNV dbSNP153 33..33 33 - - - 90280 RMVar_ID_90280 Human_SNP_ID_703496952 m1A Human chr22 + 37566676 37566676 37566676 ATGGCATCTCCCCCTGCACCCTCCCCGGCTCCACCGGCCATCTCCCCCATCATCAAGAACGCCAT ATGGCATCTCCCCCTGCACCCTCCCCGGCTCCGCCGGCCATCTCCCCCATCATCAAGAACGCCAT A G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr22:37566451..37566750;chr22:37566629..37566736 26863196 MeRIP-seq:(Medium) rs745922297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400021,Human_RBP_ID_17671122,Human_RBP_ID_17701951,Human_RBP_ID_18953009,Human_RBP_ID_27493684 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90281 RMVar_ID_90281 Human_SNP_ID_703496955 m1A Human chr22 + 37566702 37566679 37566703 GGCTCCACCGGCCATCTCCCCCATCATCAAGAACGCCATCTCCCTGCCCCAGCTCAACCAGGCCG GGCTCCACCG________________________GCCATCTCCCTGCCCCAGCTCAACCAGGCCG GGCCATCTCCCCCATCATCAAGAAC G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37566432..37566834 26863196 MeRIP-seq:(Medium) rs767836939 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_579493,Human_RBP_ID_17400021,Human_RBP_ID_17660523,Human_RBP_ID_17671122,Human_RBP_ID_18952598,Human_RBP_ID_27036763,Human_RBP_ID_27493684 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90282 RMVar_ID_90282 Human_SNP_ID_703496960 m1A Human chr22 - 37566686 37566686 37566686 GGGCAGGGAGATGGCGTTCTTGATGATGGGGGAGATGGCCGGTGGAGCCGGGGAGGGTGCAGGGG GGGCAGGGAGATGGCGTTCTTGATGATGGGGGCGATGGCCGGTGGAGCCGGGGAGGGTGCAGGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37566438..37566725 26863196 MeRIP-seq:(Medium) rs768436129 Functional Loss SNV dbSNP153 33..33 33 - - - 90283 RMVar_ID_90283 Human_SNP_ID_703496966 m1A Human chr22 + 37566692 37566690 37566693 CACCCTCCCCGGCTCCACCGGCCATCTCCCCCATCATCAAGAACGCCATCTCCCTGCCCCAGCTC CACCCTCCCCGGCTCCACCGGCCATCTCCCC___CATCAAGAACGCCATCTCCCTGCCCCAGCTC CCAT C CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37566426..37566750 26863196 MeRIP-seq:(Medium) rs1238337800 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5424428,Human_RBP_ID_17400021,Human_RBP_ID_17671122,Human_RBP_ID_18953009,Human_RBP_ID_27493684 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90284 RMVar_ID_90284 Human_SNP_ID_703496967 m1A Human chr22 + 37566692 37566692 37566692 CACCCTCCCCGGCTCCACCGGCCATCTCCCCCATCATCAAGAACGCCATCTCCCTGCCCCAGCTC CACCCTCCCCGGCTCCACCGGCCATCTCCCCCGTCATCAAGAACGCCATCTCCCTGCCCCAGCTC A G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37566426..37566750 26863196 MeRIP-seq:(Medium) rs148893156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5424428,Human_RBP_ID_17400021,Human_RBP_ID_17671122,Human_RBP_ID_18953009,Human_RBP_ID_27493684 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90285 RMVar_ID_90285 Human_SNP_ID_703496997 m1A Human chr22 + 37566776 37566768 37566776 GCCTCGTGGTTGGCAAGCTCAGCTTCGACAGCAGCCCCACCAGCTCCACGGACGGCCACTCCAGC GCCTCGTGGTTGGCAAGCTCAGCTT________GCCCCACCAGCTCCACGGACGGCCACTCCAGC TCGACAGCA T CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:37566751..37566775 26863196 MeRIP-seq:(Medium) rs1250246174 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_17400021,Human_RBP_ID_26822487 Human_Splice_Rec_2164073 Human_miRNA_ID_1420480,Human_miRNA_ID_2053062 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90286 RMVar_ID_90286 Human_SNP_ID_703497003 m1A Human chr22 + 37566773 37566773 37566773 ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACAGCAGCCCCACCAGCTCCACGGACGGCCACTCC ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACCGCAGCCCCACCAGCTCCACGGACGGCCACTCC A C CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37566724..37568119 32194978 MeRIP-seq:(Medium) rs1480164089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400021,Human_RBP_ID_26822487,Human_RBP_ID_27307556 Human_Splice_Rec_2164073 Human_miRNA_ID_1420480,Human_miRNA_ID_2053062 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90287 RMVar_ID_90287 Human_SNP_ID_703497004 m1A Human chr22 + 37566773 37566773 37566773 ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACAGCAGCCCCACCAGCTCCACGGACGGCCACTCC ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACGGCAGCCCCACCAGCTCCACGGACGGCCACTCC A G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37566724..37568119 32194978 MeRIP-seq:(Medium) rs1480164089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400021,Human_RBP_ID_26822487,Human_RBP_ID_27307556 Human_Splice_Rec_2164073 Human_miRNA_ID_1420480,Human_miRNA_ID_2053062 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90288 RMVar_ID_90288 Human_SNP_ID_703497005 m1A Human chr22 + 37566773 37566773 37566773 ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACAGCAGCCCCACCAGCTCCACGGACGGCCACTCC ACAGCCTCGTGGTTGGCAAGCTCAGCTTCGACTGCAGCCCCACCAGCTCCACGGACGGCCACTCC A T CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37566724..37568119 32194978 MeRIP-seq:(Medium) rs1480164089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400021,Human_RBP_ID_26822487,Human_RBP_ID_27307556 Human_Splice_Rec_2164073 Human_miRNA_ID_1420480,Human_miRNA_ID_2053062 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_354192,RMVar_hsa_circ_214165 90289 RMVar_ID_90289 Human_SNP_ID_703497310 m1A Human chr22 - 37568118 37568117 37568119 GAGCGGGGCAGGCGGGAGATGGTGCAGAACCCAGAGTCCAGGCCTAGAAGAGAAATGGGCAGTGG GAGCGGGGCAGGCGGGAGATGGTGCAGAACC__GAGTCCAGGCCTAGAAGAGAAATGGGCAGTGG CTG C lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37568102..37568466 26863196 MeRIP-seq:(Medium) rs1247496234 Functional Loss DEL dbSNP153 32..33 33 - - - 90290 RMVar_ID_90290 Human_SNP_ID_703497335 m1A Human chr22 + 37568162 37568162 37568162 CATCTCCCGCCTGCCCCGCTCGGAAAAGCCGCATGACCGAGACCGGGATGGTTCCTTCCCCTCTG CATCTCCCGCCTGCCCCGCTCGGAAAAGCCGCGTGACCGAGACCGGGATGGTTCCTTCCCCTCTG A G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:37568101..37568335 26863196 MeRIP-seq:(Medium) rs1051192080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8549684,Human_RBP_ID_17400023,Human_RBP_ID_18953011 Human_Splice_Rec_2164074 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_113182,RMVar_hsa_circ_214165,RMVar_hsa_circ_214166 90291 RMVar_ID_90291 Human_SNP_ID_703497364 m1A Human chr22 + 37568216 37568216 37568216 CTTCCCCTCTGAGCCCGGGCTTCGCCGCTCTGACTCTCTCTTGTCCTTCCGCCTGGACCTCGACC CTTCCCCTCTGAGCCCGGGCTTCGCCGCTCTGTCTCTCTCTTGTCCTTCCGCCTGGACCTCGACC A T CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37568101..37568450 26863196 MeRIP-seq:(Medium) rs1383224936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781530,Human_RBP_ID_2718073,Human_RBP_ID_9332833,Human_RBP_ID_17400023,Human_RBP_ID_18952599,Human_RBP_ID_22533836,Human_RBP_ID_27307562,Human_RBP_ID_27493689 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_113182,RMVar_hsa_circ_214165,RMVar_hsa_circ_214166 90292 RMVar_ID_90292 Human_SNP_ID_703497417 m1A Human chr22 - 37568367 37568325 37568367 GGGTTTGCAGTAGTGGCTGGGGGGTTTGCAGCAGGACCCGTGGGGTTTGCAGTAGGGGCTGGGGG GGGTTTGCAGTAGTGGCTGGGGGGTTTGCAGC_________________________________ CGCTGCAAACCCCCCAGCCCCTACTGCAAACCCCACGGGTCCT C lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:37568278..37568367 26863410 MeRIP-seq:(Medium) rs752645135 Functional Loss DEL dbSNP153 33..65 33 - - - 90293 RMVar_ID_90293 Human_SNP_ID_703497448 m1A Human chr22 - 37568367 37568347 37568368 GGGTTTGCAGTAGTGGCTGGGGGGTTTGCAGCAGGACCCGTGGGGTTTGCAGTAGGGGCTGGGGG GGGTTTGCAGTAGTGGCTGGGGGGTTTGCAG_____________________TAGGGGCTGGGGG ACTGCAAACCCCACGGGTCCTG A lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:37568278..37568367 26863410 MeRIP-seq:(Medium) rs780789435 Functional Loss DEL dbSNP153 32..52 33 - - - 90294 RMVar_ID_90294 Human_SNP_ID_703497659 m1A Human chr22 - 37568645 37568645 37568645 GCAGCACCTCCACCCGCTCCTGCCGCGCATCCATCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT GCAGCACCTCCACCCGCTCCTGCCGCGCATCCTTCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT T A lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37568596..37568889 26863196 MeRIP-seq:(Medium) rs753174629 Functional Loss SNV dbSNP153 33..33 33 - - - 90295 RMVar_ID_90295 Human_SNP_ID_703497660 m1A Human chr22 - 37568645 37568645 37568645 GCAGCACCTCCACCCGCTCCTGCCGCGCATCCATCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT GCAGCACCTCCACCCGCTCCTGCCGCGCATCCGTCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT T C lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37568596..37568889 26863196 MeRIP-seq:(Medium) rs753174629 Functional Loss SNV dbSNP153 33..33 33 - - - 90296 RMVar_ID_90296 Human_SNP_ID_703497661 m1A Human chr22 - 37568645 37568645 37568645 GCAGCACCTCCACCCGCTCCTGCCGCGCATCCATCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT GCAGCACCTCCACCCGCTCCTGCCGCGCATCCCTCTCTGGGTAGTGGTGGCCGCCATCCCAGCCT T G lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37568596..37568889 26863196 MeRIP-seq:(Medium) rs753174629 Functional Loss SNV dbSNP153 33..33 33 - - - 90297 RMVar_ID_90297 Human_SNP_ID_703497673 m1A Human chr22 - 37568675 37568675 37568675 CCAGGCTCTCCCAGGAGGCCCGGGCTTGGGGCAGCACCTCCACCCGCTCCTGCCGCGCATCCATC CCAGGCTCTCCCAGGAGGCCCGGGCTTGGGGCGGCACCTCCACCCGCTCCTGCCGCGCATCCATC T C lnc-LGALS2-2 RNACentral:URS00008C333C lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37568626..37568700 26863196 MeRIP-seq:(Medium) rs200126736 Functional Loss SNV dbSNP153 33..33 33 - - - 90298 RMVar_ID_90298 Human_SNP_ID_703509031 m1A Human chr22 - 37609050 37609050 37609050 GGGGCCGGGGTCCTCCATCGCTCCAGGGTCTGAGGGGCCGACTGAGGACACCGCCCCTCCCGGGC GGGGCCGGGGTCCTCCATCGCTCCAGGGTCTGGGGGGCCGACTGAGGACACCGCCCCTCCCGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37609013..37609420 26863196 MeRIP-seq:(Medium) rs1038678916 Functional Loss SNV dbSNP153 33..33 33 - - - 90299 RMVar_ID_90299 Human_SNP_ID_703509430 m1A Human chr22 - 37610098 37610098 37610098 AGCTCAAGACCTGTGTCTGAGATCAGTTAGCCAGGGGCCCACCCATCCCCCCAGCCCAGTTGCTG AGCTCAAGACCTGTGTCTGAGATCAGTTAGCCGGGGGCCCACCCATCCCCCCAGCCCAGTTGCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37610088..37610157 26863196 MeRIP-seq:(Medium) rs771046078 Functional Loss SNV dbSNP153 33..33 33 - - - 90300 RMVar_ID_90300 Human_SNP_ID_703513606 m1A Human chr22 + 37624584 37624584 37624584 TGGTGAGTGGCATGGAGGAAGAGAAGCAGGGAAGGGATGAGGTGGTGCAGGAGGGATTTAGGACA TGGTGAGTGGCATGGAGGAAGAGAAGCAGGGAGGGGATGAGGTGGTGCAGGAGGGATTTAGGACA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37624579..37624858 26863196 MeRIP-seq:(Medium) rs1006634352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15720,RMVar_hsa_circ_8893,RMVar_hsa_circ_27104,RMVar_hsa_circ_375810,RMVar_hsa_circ_113618,RMVar_hsa_circ_214169,RMVar_hsa_circ_17322,RMVar_hsa_circ_214170,RMVar_hsa_circ_214168,RMVar_hsa_circ_214175,RMVar_hsa_circ_75698,RMVar_hsa_circ_25129,RMVar_hsa_circ_313343,RMVar_hsa_circ_214173 90301 RMVar_ID_90301 Human_SNP_ID_703515339 m1A Human chr22 - 37630995 37630995 37630995 GCCTGGGGGGCTCTGGGGACACGGTGTGGAGAAGGCTGGTGGCGCTGGAGCTGGGGGAGCTGCAG GCCTGGGGGGCTCTGGGGACACGGTGTGGAGACGGCTGGTGGCGCTGGAGCTGGGGGAGCTGCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37630865..37631031 26863196 MeRIP-seq:(Medium) rs1218305859 Functional Loss SNV dbSNP153 33..33 33 - - - 90302 RMVar_ID_90302 Human_SNP_ID_703515341 m1A Human chr22 - 37630998 37630998 37630998 GAGGCCTGGGGGGCTCTGGGGACACGGTGTGGAGAAGGCTGGTGGCGCTGGAGCTGGGGGAGCTG GAGGCCTGGGGGGCTCTGGGGACACGGTGTGGGGAAGGCTGGTGGCGCTGGAGCTGGGGGAGCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37630947..37631039 26863196 MeRIP-seq:(Medium) rs1418215687 Functional Loss SNV dbSNP153 33..33 33 - - - 90303 RMVar_ID_90303 Human_SNP_ID_703517745 m1A Human chr22 + 37639501 37639500 37639501 GGGCACAACCTGTGGACGGCCGCGGCCGGCGGACACACAGCAGCGGGGGCCCGGCCGGGGGTCGC GGGCACAACCTGTGGACGGCCGCGGCCGGCGG_CACACAGCAGCGGGGGCCCGGCCGGGGGTCGC GA G SH3BP1 Ensembl:ENSG00000100092 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37639493..37639666 26863196 MeRIP-seq:(Medium) rs1318649962 Functional Loss DEL dbSNP153 33..33 33 - - - 90304 RMVar_ID_90304 Human_SNP_ID_703519137 m1A Human chr22 + 37643672 37643672 37643672 CCAGGCTCAGTCAGGCAACCAAGAATTCAGGCAGCAGTCAAGGCCTAGGAGGCAGCCCGGGTAGT CCAGGCTCAGTCAGGCAACCAAGAATTCAGGCGGCAGTCAAGGCCTAGGAGGCAGCCCGGGTAGT A G SH3BP1,Z83844.3 Ensembl:ENSG00000100092,Ensembl:ENSG00000285304 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37643668..37643769 32194978 MeRIP-seq:(Medium) rs770363885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2164366,Human_Splice_Rec_2164402,Human_Splice_Rec_2164436,Human_Splice_Rec_2164466,Human_Splice_Rec_2164496,Human_Splice_Rec_2164566 RMVar_hsa_circ_25557,RMVar_hsa_circ_117648,RMVar_hsa_circ_32571,RMVar_hsa_circ_214180,RMVar_hsa_circ_214181,RMVar_hsa_circ_114542 90305 RMVar_ID_90305 Human_SNP_ID_703521233 m1A Human chr22 + 37650598 37650598 37650598 TCTTCTCAGCTGTTACCCTCCAGGACACAGTCAGTGACAGGCTGGCCTCTGAGGAACTTCCGTCC TCTTCTCAGCTGTTACCCTCCAGGACACAGTCGGTGACAGGCTGGCCTCTGAGGAACTTCCGTCC A G SH3BP1,Z83844.3 Ensembl:ENSG00000100092,Ensembl:ENSG00000285304 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37650217..37650609 32194978 MeRIP-seq:(Medium) rs931931282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3962371,Human_RBP_ID_9392929 Human_Splice_Rec_2164384,Human_Splice_Rec_2164420,Human_Splice_Rec_2164456,Human_Splice_Rec_2164484,Human_Splice_Rec_2164532,Human_Splice_Rec_2164542,Human_Splice_Rec_2164552,Human_Splice_Rec_2164584 Human_miRNA_ID_2225906,Human_miRNA_ID_2398731 RMVar_hsa_circ_117648,RMVar_hsa_circ_32571,RMVar_hsa_circ_214180,RMVar_hsa_circ_214181,RMVar_hsa_circ_114542,RMVar_hsa_circ_81114,RMVar_hsa_circ_60235,RMVar_hsa_circ_98260,RMVar_hsa_circ_214183,RMVar_hsa_circ_91112,RMVar_hsa_circ_214184,RMVar_hsa_circ_79359,RMVar_hsa_circ_109908,RMVar_hsa_circ_214185,RMVar_hsa_circ_214186,RMVar_hsa_circ_115180,RMVar_hsa_circ_214187,RMVar_hsa_circ_214188,RMVar_hsa_circ_214189,RMVar_hsa_circ_301272,RMVar_hsa_circ_308965 90306 RMVar_ID_90306 Human_SNP_ID_703522514 m1A Human chr22 - 37655375 37655375 37655375 ACCAGACGTCGGGGCAGGGCTTGGGGGGTCCCAGGGCTGCCAGAGCCAGGGGGCAAGGGCGGGGC ACCAGACGTCGGGGCAGGGCTTGGGGGGTCCCCGGGCTGCCAGAGCCAGGGGGCAAGGGCGGGGC T G Z83844.2 Ensembl:ENSG00000233360 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:37655276..37655525 26863410 MeRIP-seq:(Medium) rs950481881 Functional Loss SNV dbSNP153 33..33 33 - - - 90307 RMVar_ID_90307 Human_SNP_ID_703523783 m1A Human chr22 + 37658841 37658841 37658841 AGCGGCCCTGCGCGACGTGCTGGGCCGGGCGCAGGGGGTCCTGTTCGACTGTGACGGGGTGCTGT AGCGGCCCTGCGCGACGTGCTGGGCCGGGCGCTGGGGGTCCTGTTCGACTGTGACGGGGTGCTGT A T Z83844.3,PDXP Ensembl:ENSG00000285304,Ensembl:ENSG00000241360 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37658726..37658924 26863196 MeRIP-seq:(Medium) rs1256701746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579559,Human_RBP_ID_4708201,Human_RBP_ID_5119744,Human_RBP_ID_5389242,Human_RBP_ID_7080038,Human_RBP_ID_8943173,Human_RBP_ID_18194359,Human_RBP_ID_23134394,Human_RBP_ID_27493719 Human_miRNA_ID_2660668,Human_miRNA_ID_2660669 RMVar_hsa_circ_117648,RMVar_hsa_circ_214180,RMVar_hsa_circ_214181,RMVar_hsa_circ_114542,RMVar_hsa_circ_81114,RMVar_hsa_circ_98260,RMVar_hsa_circ_214183,RMVar_hsa_circ_91112,RMVar_hsa_circ_214184,RMVar_hsa_circ_79359,RMVar_hsa_circ_109908,RMVar_hsa_circ_214185,RMVar_hsa_circ_214186,RMVar_hsa_circ_214187,RMVar_hsa_circ_98281,RMVar_hsa_circ_214190 90308 RMVar_ID_90308 Human_SNP_ID_703523881 m1A Human chr22 - 37659081 37659081 37659081 ACACGGCGCCCGGCGCGTCCGGAGGCCCGGGCAGGCGCTGGCGCAGCAGGCGCGCGGCGCACAGC ACACGGCGCCCGGCGCGTCCGGAGGCCCGGGCTGGCGCTGGCGCAGCAGGCGCGCGGCGCACAGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37659034..37659190 26863196 MeRIP-seq:(Medium) rs1406970252 Functional Loss SNV dbSNP153 33..33 33 - - - 90309 RMVar_ID_90309 Human_SNP_ID_703524010 m1A Human chr22 + 37659350 37659350 37659350 ACCCATGGCACCCGCTGAGCGACGGCAGCCGGACCCCTGGTGAGCGCGGGAATGGCGGGGAAACT ACCCATGGCACCCGCTGAGCGACGGCAGCCGGGCCCCTGGTGAGCGCGGGAATGGCGGGGAAACT A G Z83844.3,PDXP Ensembl:ENSG00000285304,Ensembl:ENSG00000241360 Protein coding,Protein coding intron,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37659176..37659436 26863196 MeRIP-seq:(Medium) rs1316794932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930941,Human_RBP_ID_18194360 Human_Splice_Rec_2164599 RMVar_hsa_circ_117648,RMVar_hsa_circ_214180,RMVar_hsa_circ_214181,RMVar_hsa_circ_114542,RMVar_hsa_circ_81114,RMVar_hsa_circ_98260,RMVar_hsa_circ_214183,RMVar_hsa_circ_91112,RMVar_hsa_circ_214184,RMVar_hsa_circ_79359,RMVar_hsa_circ_109908,RMVar_hsa_circ_214185,RMVar_hsa_circ_214186,RMVar_hsa_circ_214187,RMVar_hsa_circ_98281,RMVar_hsa_circ_214190 90310 RMVar_ID_90310 Human_SNP_ID_703524014 m1A Human chr22 - 37659358 37659358 37659358 CCCATCTCAGTTTCCCCGCCATTCCCGCGCTCACCAGGGGTCCGGCTGCCGTCGCTCAGCGGGTG CCCATCTCAGTTTCCCCGCCATTCCCGCGCTCCCCAGGGGTCCGGCTGCCGTCGCTCAGCGGGTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37658755..37664966 26863196 MeRIP-seq:(Medium) rs761395648 Functional Loss SNV dbSNP153 33..33 33 - - - 90311 RMVar_ID_90311 Human_SNP_ID_703525946 m1A Human chr22 - 37666036 37666036 37666036 GGGGCAGCAAAGAGTGCCCAGCCACTGCTGGGAGGGGGTTGCAAGGGCCCTCAAACCTTCCCCGG GGGGCAGCAAAGAGTGCCCAGCCACTGCTGGGGGGGGGTTGCAAGGGCCCTCAAACCTTCCCCGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37665986..37666385 32194978 MeRIP-seq:(Medium) rs375355102 Functional Loss SNV dbSNP153 33..33 33 - - - 90312 RMVar_ID_90312 Human_SNP_ID_703528611 m1A Human chr22 - 37675711 37675711 37675711 CCTGGACCTTGGGGGGGGGTCCCCACACTCACACAAGCCATGATTGAGTCCAGGAGGATGTTCCC CCTGGACCTTGGGGGGGGGTCCCCACACTCACGCAAGCCATGATTGAGTCCAGGAGGATGTTCCC T C lnc-LGALS2-5 RNACentral:URS0000D58E84 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37675701..37675725 26863196 MeRIP-seq:(Medium) rs1349210218 Functional Loss SNV dbSNP153 33..33 33 - - - 90313 RMVar_ID_90313 Human_SNP_ID_703529014 m1A Human chr22 - 37676979 37676979 37676979 AGATTCAGGTTGCTGGCGACCAGACCCTGCACAGACAAGCCCCGGCCCAGCCGGGTTAGAGGACA AGATTCAGGTTGCTGGCGACCAGACCCTGCACGGACAAGCCCCGGCCCAGCCGGGTTAGAGGACA T C lnc-LGALS2-5 RNACentral:URS0000D58E84 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr22:37676976..37677075;chr22:37676976..37677025;chr22:37676976..37677087 26863196,32194978 MeRIP-seq:(Medium) rs990552902 Functional Loss SNV dbSNP153 33..33 33 - - - 90314 RMVar_ID_90314 Human_SNP_ID_703529492 m1A Human chr22 + 37678533 37678533 37678533 CAAAGACAGCAACAACCTGTGCCTGCACTTCAACCCTCGCTTCAACGCCCACGGCGACGCCAACA CAAAGACAGCAACAACCTGTGCCTGCACTTCAGCCCTCGCTTCAACGCCCACGGCGACGCCAACA A G LGALS1 Ensembl:ENSG00000100097 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:37678428..37678686;chr22:37678414..37678694 26863196 MeRIP-seq:(Medium) rs1265478596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64985,Human_RBP_ID_781130 Human_Splice_Rec_2164606,Human_Splice_Rec_2164614,Human_Splice_Rec_2164626,Human_Splice_Rec_2164632 Human_miRNA_ID_2294641 RMVar_hsa_circ_43742,RMVar_hsa_circ_85396,RMVar_hsa_circ_115177,RMVar_hsa_circ_214193,RMVar_hsa_circ_214194,RMVar_hsa_circ_112388,RMVar_hsa_circ_333727,RMVar_hsa_circ_214195 90315 RMVar_ID_90315 Human_SNP_ID_703529498 m1A Human chr22 - 37678541 37678541 37678541 CACGATGGTGTTGGCGTCGCCGTGGGCGTTGAAGCGAGGGTTGAAGTGCAGGCACAGGTTGTTGC CACGATGGTGTTGGCGTCGCCGTGGGCGTTGAGGCGAGGGTTGAAGTGCAGGCACAGGTTGTTGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr22:37678407..37678561;chr22:37678476..37678600;chr22:37678451..37679775 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 90316 RMVar_ID_90316 Human_SNP_ID_703529908 m1A Human chr22 + 37679673 37679673 37679673 GCTGCCAGATGGATACGAATTCAAGTTCCCCAACCGCCTCAACCTGGAGGCCATCAACTACATGG GCTGCCAGATGGATACGAATTCAAGTTCCCCAGCCGCCTCAACCTGGAGGCCATCAACTACATGG A G LGALS1 Ensembl:ENSG00000100097 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37679651..37679675 32194978 MeRIP-seq:(Medium) rs771790822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64986,Human_RBP_ID_151905,Human_RBP_ID_17660289,Human_RBP_ID_22768131,Human_RBP_ID_24494013,Human_RBP_ID_26822490,Human_RBP_ID_27493743 Human_Splice_Rec_2164608,Human_Splice_Rec_2164616,Human_Splice_Rec_2164628,Human_Splice_Rec_2164634,Human_Splice_Rec_2164638 RMVar_hsa_circ_85396,RMVar_hsa_circ_115177,RMVar_hsa_circ_214193,RMVar_hsa_circ_214194,RMVar_hsa_circ_95971,RMVar_hsa_circ_112388,RMVar_hsa_circ_214195,RMVar_hsa_circ_214196 90317 RMVar_ID_90317 Human_SNP_ID_703531682 m1A Human chr22 - 37686445 37686445 37686445 ACCGCCTCTTCTCCTCGTCGAAGCTAAGAACGAGCCTCGGCCGCCGGTCGTCACCATCTCGCTTC ACCGCCTCTTCTCCTCGTCGAAGCTAAGAACGCGCCTCGGCCGCCGGTCGTCACCATCTCGCTTC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:37686396..37687997 26863196 MeRIP-seq:(Medium) rs755902475 Functional Loss SNV dbSNP153 33..33 33 - - - 90318 RMVar_ID_90318 Human_SNP_ID_703531686 m1A Human chr22 - 37686452 37686452 37686452 GCCACTCACCGCCTCTTCTCCTCGTCGAAGCTAAGAACGAGCCTCGGCCGCCGGTCGTCACCATC GCCACTCACCGCCTCTTCTCCTCGTCGAAGCTGAGAACGAGCCTCGGCCGCCGGTCGTCACCATC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37686403..37686538 26863196 MeRIP-seq:(Medium) rs748837306 Functional Loss SNV dbSNP153 33..33 33 - - - 90319 RMVar_ID_90319 Human_SNP_ID_703532339 m1A Human chr22 + 37688343 37688343 37688343 GCGCCACCAGGAATACTTGAAGATGCTGGCAGAGAGAGAAGAGGCTCTGGGTAAGTGGCATGCTT GCGCCACCAGGAATACTTGAAGATGCTGGCAGGGAGAGAAGAGGCTCTGGGTAAGTGGCATGCTT A G NOL12,Z83844.1 Ensembl:ENSG00000273899,Ensembl:ENSG00000100101 Protein coding,Protein coding exon,CDS GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr22:37687996..37688881;chr22:37687996..37690733 26863196,32194978 MeRIP-seq:(Medium) rs1325714544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245754,Human_RBP_ID_781134,Human_RBP_ID_833999,Human_RBP_ID_929870,Human_RBP_ID_3962374,Human_RBP_ID_9392334,Human_RBP_ID_14477410,Human_RBP_ID_17660013,Human_RBP_ID_17985798,Human_RBP_ID_19112042,Human_RBP_ID_26345405,Human_RBP_ID_27821295 Human_Splice_Rec_2164642,Human_Splice_Rec_2164643,Human_Splice_Rec_2164654,Human_Splice_Rec_2164655,Human_Splice_Rec_2164668,Human_Splice_Rec_2164669,Human_Splice_Rec_2164678,Human_Splice_Rec_2164679,Human_Splice_Rec_2164686,Human_Splice_Rec_2164687,Human_Splice_Rec_2164696,Human_Splice_Rec_2164697,Human_Splice_Rec_2164706,Human_Splice_Rec_2164707 RMVar_hsa_circ_43013,RMVar_hsa_circ_286101,RMVar_hsa_circ_307902,RMVar_hsa_circ_214198,RMVar_hsa_circ_104014,RMVar_hsa_circ_214199 90320 RMVar_ID_90320 Human_SNP_ID_703544291 m1A Human chr22 - 37726235 37726235 37726235 TAGGTCACTGGGTGGGTGGCGGGGTGGGGAGGAGGCTCGGGGTGCATCCCGGTGCCCGATGCACA TAGGTCACTGGGTGGGTGGCGGGGTGGGGAGGCGGCTCGGGGTGCATCCCGGTGCCCGATGCACA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37726106..37726257 32194978 MeRIP-seq:(Medium) rs752210243 Functional Loss SNV dbSNP153 33..33 33 - - - 90321 RMVar_ID_90321 Human_SNP_ID_703549982 m1A Human chr22 + 37746451 37746451 37746451 CGGTGAGTGCCCCAGTCAGCCGCCCGCGCCCGAGGCCGGGAGAAGGGCGACGACCCGAGGCAGAG CGGTGAGTGCCCCAGTCAGCCGCCCGCGCCCGTGGCCGGGAGAAGGGCGACGACCCGAGGCAGAG A T TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:37746403..37746716 26863196 MeRIP-seq:(Medium) rs1283307787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19113296 RMVar_hsa_circ_122088,RMVar_hsa_circ_214202 90322 RMVar_ID_90322 Human_SNP_ID_703550054 m1A Human chr22 + 37746584 37746584 37746584 GACGGGGCCACCTCCGAAGCGCTTTCGGCCAGACCGGCCTCACCCTTCCCGCAGGCTCCTCCTCG GACGGGGCCACCTCCGAAGCGCTTTCGGCCAGTCCGGCCTCACCCTTCCCGCAGGCTCCTCCTCG A T TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37746578..37746739 32194978 MeRIP-seq:(Medium) rs1569052320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122088,RMVar_hsa_circ_214202 90323 RMVar_ID_90323 Human_SNP_ID_703551458 m1A Human chr22 - 37751755 37751752 37751755 AGTTGAGCAGATCGGGCTGTGGGGAGATGAGGAGGGAGGTGAGTTGGGTCCAGCAGGAAGCCAAT AGTTGAGCAGATCGGGCTGTGGGGAGATGAGG___GAGGTGAGTTGGGTCCAGCAGGAAGCCAAT CCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37751751..37751850 26863196 MeRIP-seq:(Medium) rs775184499 Functional Loss DEL dbSNP153 33..35 33 - - - 90324 RMVar_ID_90324 Human_SNP_ID_703553399 m1A Human chr22 - 37757990 37757990 37757990 GCTCCTGCCACTTCTTCTCGATCTCCTCACTAAGCCGGTTTTGCTGGTCCTCAGTCAGGGGGGCA GCTCCTGCCACTTCTTCTCGATCTCCTCACTATGCCGGTTTTGCTGGTCCTCAGTCAGGGGGGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37757939..37758097 26863196 MeRIP-seq:(Medium) rs1310561645 Functional Loss SNV dbSNP153 33..33 33 - - - 90325 RMVar_ID_90325 Human_SNP_ID_703554441 m1A Human chr22 + 37761476 37761473 37761477 CTAAAAACAGCAACAAAAAACAAAACAAACAAAAAAAGAGAAGCTCATTCCACAGACTTTTGGAG CTAAAAACAGCAACAAAAAACAAAACAAAC____AAAGAGAAGCTCATTCCACAGACTTTTGGAG CAAAA C TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37761474..37761653 26863196 MeRIP-seq:(Medium) rs1026616036 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_82349,RMVar_hsa_circ_34450,RMVar_hsa_circ_214208,RMVar_hsa_circ_78716,RMVar_hsa_circ_214207,RMVar_hsa_circ_27849 90326 RMVar_ID_90326 Human_SNP_ID_703554442 m1A Human chr22 + 37761476 37761473 37761477 CTAAAAACAGCAACAAAAAACAAAACAAACAAAAAAAGAGAAGCTCATTCCACAGACTTTTGGAG CTAAAAACAGCAACAAAAAACAAAACAAACAA__AAAGAGAAGCTCATTCCACAGACTTTTGGAG CAAAA CAA TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37761474..37761653 26863196 MeRIP-seq:(Medium) rs1026616036 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_82349,RMVar_hsa_circ_34450,RMVar_hsa_circ_214208,RMVar_hsa_circ_78716,RMVar_hsa_circ_214207,RMVar_hsa_circ_27849 90327 RMVar_ID_90327 Human_SNP_ID_703554778 m1A Human chr22 + 37762755 37762755 37762755 GAGTCATCTGTATCGCCCTCAGGCACGGGAGGAGGCGGATGGAAATTCGGTGGACCTGGAGGAGT GAGTCATCTGTATCGCCCTCAGGCACGGGAGGCGGCGGATGGAAATTCGGTGGACCTGGAGGAGT A C TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:37762654..37762783 26863196 MeRIP-seq:(Medium) rs922463175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82349,RMVar_hsa_circ_34450,RMVar_hsa_circ_214208,RMVar_hsa_circ_78716,RMVar_hsa_circ_214207,RMVar_hsa_circ_27849 90328 RMVar_ID_90328 Human_SNP_ID_703555504 m1A Human chr22 + 37765410 37765410 37765410 GCTTGGCAGAGAAAGGCCAGGGATGAGAACGTAAAGGTCAGCCATGGGAACGGGGACTTGACTCT GCTTGGCAGAGAAAGGCCAGGGATGAGAACGTCAAGGTCAGCCATGGGAACGGGGACTTGACTCT A C TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37765408..37765650 26863196 MeRIP-seq:(Medium) rs1433707334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8549790,Human_RBP_ID_18788655 RMVar_hsa_circ_82349,RMVar_hsa_circ_34450,RMVar_hsa_circ_214208,RMVar_hsa_circ_78716,RMVar_hsa_circ_214207,RMVar_hsa_circ_27849 90329 RMVar_ID_90329 Human_SNP_ID_703555505 m1A Human chr22 + 37765410 37765410 37765410 GCTTGGCAGAGAAAGGCCAGGGATGAGAACGTAAAGGTCAGCCATGGGAACGGGGACTTGACTCT GCTTGGCAGAGAAAGGCCAGGGATGAGAACGTGAAGGTCAGCCATGGGAACGGGGACTTGACTCT A G TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37765408..37765650 26863196 MeRIP-seq:(Medium) rs1433707334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8549790,Human_RBP_ID_18788655 RMVar_hsa_circ_82349,RMVar_hsa_circ_34450,RMVar_hsa_circ_214208,RMVar_hsa_circ_78716,RMVar_hsa_circ_214207,RMVar_hsa_circ_27849 90330 RMVar_ID_90330 Human_SNP_ID_703555517 m1A Human chr22 - 37765488 37765488 37765488 CCCCACCCCACGGCTCCTCATTCACAAACCTCACCTTGTCGCTCCTGCCTCAAGCCCTCCAGGGA CCCCACCCCACGGCTCCTCATTCACAAACCTCGCCTTGTCGCTCCTGCCTCAAGCCCTCCAGGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37765480..37765636 26863196 MeRIP-seq:(Medium) rs956572199 Functional Loss SNV dbSNP153 33..33 33 - - - 90331 RMVar_ID_90331 Human_SNP_ID_703558595 m1A Human chr22 - 37775426 37775426 37775426 TCCTCCACCCCACTCCCAAGACTTCCCCTCGCATTTCACTGGCTTGCGTGAACTGCAAGCCTTGT TCCTCCACCCCACTCCCAAGACTTCCCCTCGCCTTTCACTGGCTTGCGTGAACTGCAAGCCTTGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37775376..37775508 26863196 MeRIP-seq:(Medium) rs954788998 Functional Loss SNV dbSNP153 33..33 33 - - - 90332 RMVar_ID_90332 Human_SNP_ID_703567300 m1A Human chr22 + 37805758 37805758 37805758 GTGAGAACGCTGACTCGCAGATCAAGTTGTCCATCAAGCGCCTGGTCACCACCGGTGTCCTCAAG GTGAGAACGCTGACTCGCAGATCAAGTTGTCCCTCAAGCGCCTGGTCACCACCGGTGTCCTCAAG A C H1-0 Ensembl:ENSG00000189060 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1171521150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1611141,Human_RBP_ID_4696304,Human_RBP_ID_9392349 90333 RMVar_ID_90333 Human_SNP_ID_703567383 m1A Human chr22 - 37805972 37805972 37805972 GCGTGGCAGCCAGCTTCTTCTTGGCCTTCTTGACCGGGGTGGCTTTGGGTTTCTTGGTTGGGGCT GCGTGGCAGCCAGCTTCTTCTTGGCCTTCTTGGCCGGGGTGGCTTTGGGTTTCTTGGTTGGGGCT T C lnc-ANKRD54-1 RNACentral:URS0000D5C511 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37805926..37805975 26863196 MeRIP-seq:(Medium) rs1178816000 Functional Loss SNV dbSNP153 33..33 33 - - - 90334 RMVar_ID_90334 Human_SNP_ID_703567384 m1A Human chr22 - 37805972 37805972 37805972 GCGTGGCAGCCAGCTTCTTCTTGGCCTTCTTGACCGGGGTGGCTTTGGGTTTCTTGGTTGGGGCT GCGTGGCAGCCAGCTTCTTCTTGGCCTTCTTGCCCGGGGTGGCTTTGGGTTTCTTGGTTGGGGCT T G lnc-ANKRD54-1 RNACentral:URS0000D5C511 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37805926..37805975 26863196 MeRIP-seq:(Medium) rs1178816000 Functional Loss SNV dbSNP153 33..33 33 - - - 90335 RMVar_ID_90335 Human_SNP_ID_703567392 m1A Human chr22 + 37805989 37805989 37805989 CCAAAGCCACCCCGGTCAAGAAGGCCAAGAAGAAGCTGGCTGCCACGCCCAAGAAAGCCAAAAAA CCAAAGCCACCCCGGTCAAGAAGGCCAAGAAGCAGCTGGCTGCCACGCCCAAGAAAGCCAAAAAA A C H1-0 Ensembl:ENSG00000189060 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1207094993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9392351,Human_RBP_ID_24547090 RMVar_hsa_circ_214211 90336 RMVar_ID_90336 Human_SNP_ID_703567655 m1A Human chr22 + 37806888 37806888 37806888 CTCTTGTTAAACCGGAGTGAAAACTTCAGGGGAAGGGTGGGGAGTCAGCCAAGTGCCTCAGTGTG CTCTTGTTAAACCGGAGTGAAAACTTCAGGGGGAGGGTGGGGAGTCAGCCAAGTGCCTCAGTGTG A G H1-0 Ensembl:ENSG00000189060 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37806837..37807000 32194978 MeRIP-seq:(Medium) rs1039719777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579671,Human_RBP_ID_7080178,Human_RBP_ID_8208293,Human_RBP_ID_23946631,Human_RBP_ID_26498190 90337 RMVar_ID_90337 Human_SNP_ID_703567684 m1A Human chr22 + 37807014 37807003 37807015 TTTCCTCTGGATTTTTGTTCCTCCTGTACAAGAGGTGTCTTTGCTTGGTTTGGTGGGGCTGCGGC TTTCCTCTGGATTTTTGTTCCT____________GTGTCTTTGCTTGGTTTGGTGGGGCTGCGGC TCCTGTACAAGAG T H1-0 Ensembl:ENSG00000189060 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:37806976..37807025 26863196 MeRIP-seq:(Medium) rs1343022399 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_579671,Human_RBP_ID_3672467,Human_RBP_ID_7080183,Human_RBP_ID_9126259,Human_RBP_ID_14477928,Human_RBP_ID_23946631 Human_miRNA_ID_1041542 90338 RMVar_ID_90338 Human_SNP_ID_703568065 m1A Human chr22 - 37808008 37808008 37808008 CCAGCGCTGACTGTGCGCGGCGGCCGCGGGGCACCCAGAAGAGTGCGGCGCGCCAGGCGTTCCCA CCAGCGCTGACTGTGCGCGGCGGCCGCGGGGCGCCCAGAAGAGTGCGGCGCGCCAGGCGTTCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:37807969..37808100;chr22:37807977..37808083 26863196 MeRIP-seq:(Medium) rs1347735806 Functional Loss SNV dbSNP153 33..33 33 - - - 90339 RMVar_ID_90339 Human_SNP_ID_703568106 m1A Human chr22 + 37808075 37808075 37808075 CAGCTGCGTGGCATTCTGGAGGGGGAGCTGGAAGGCATCCGCGGAGCTGGCACTTGGAAGAGTGA CAGCTGCGTGGCATTCTGGAGGGGGAGCTGGAGGGCATCCGCGGAGCTGGCACTTGGAAGAGTGA A G GCAT Ensembl:ENSG00000100116 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37807969..37808106 26863196 MeRIP-seq:(Medium) rs763625409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3677557,Human_RBP_ID_4708625,Human_RBP_ID_5149518,Human_RBP_ID_5324776,Human_RBP_ID_9332840,Human_RBP_ID_18788676 Human_Splice_Rec_2164913,Human_Splice_Rec_2164931,Human_Splice_Rec_2164947,Human_Splice_Rec_2164953,Human_Splice_Rec_2164957,Human_Splice_Rec_2164961,Human_Splice_Rec_2164967 RMVar_hsa_circ_101795,RMVar_hsa_circ_214213 90340 RMVar_ID_90340 Human_SNP_ID_703578819 m1A Human chr22 - 37844274 37844274 37844274 AGGGAAGTAGGTCCGTTGGTCGGTCGGGAACGAGGCTCAGGCGGCCAGGCCCGCGCGGAGCCGTT AGGGAAGTAGGTCCGTTGGTCGGTCGGGAACGGGGCTCAGGCGGCCAGGCCCGCGCGGAGCCGTT T C MIR658,ANKRD54 Ensembl:ENSG00000284197,Ensembl:ENSG00000100124 miRNA,Protein coding exon,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:37843960..37844384;chr22:37844084..37844373;chr22:37844126..37844325 26863196 MeRIP-seq:(Medium) rs1346864630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245790,Human_RBP_ID_4696455,Human_RBP_ID_17285904,Human_RBP_ID_17399103,Human_RBP_ID_17515099,Human_RBP_ID_21896403,Human_RBP_ID_21937772,Human_RBP_ID_24534506,Human_RBP_ID_24539054,Human_RBP_ID_24540346 Human_miRNA_ID_2209659 RMVar_hsa_circ_81722,RMVar_hsa_circ_214220 90341 RMVar_ID_90341 Human_SNP_ID_703580616 m1A Human chr22 - 37850005 37850003 37850005 TAAGCGTAGGGGTCATAAGCCGCCTAGAAGGAAAGAGACACAGTCAAGGACAGCCGCCAAGTCGT TAAGCGTAGGGGTCATAAGCCGCCTAGAAGGA__GAGACACAGTCAAGGACAGCCGCCAAGTCGT CTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37850001..37850025 26863196 MeRIP-seq:(Medium) rs1468834485 Functional Loss DEL dbSNP153 33..34 33 - - - 90342 RMVar_ID_90342 Human_SNP_ID_703581032 m1A Human chr22 + 37851327 37851327 37851327 ACCTTGCTTATGAACGTCAGTATGAACAGCAAACCTATCAGGTGATCCCTGAGGTGATCAAAAAC ACCTTGCTTATGAACGTCAGTATGAACAGCAAGCCTATCAGGTGATCCCTGAGGTGATCAAAAAC A G EIF3L Ensembl:ENSG00000100129 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37850526..37858604 32194978 MeRIP-seq:(Medium) rs1569109218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65004,Human_RBP_ID_579728,Human_RBP_ID_1611183,Human_RBP_ID_1942564,Human_RBP_ID_3962378,Human_RBP_ID_5424443,Human_RBP_ID_5446485,Human_RBP_ID_5473084,Human_RBP_ID_5504719,Human_RBP_ID_8549827,Human_RBP_ID_9333365,Human_RBP_ID_14478444,Human_RBP_ID_17286752,Human_RBP_ID_17399817,Human_RBP_ID_17515103,Human_RBP_ID_18445438,Human_RBP_ID_18788698,Human_RBP_ID_23212767,Human_RBP_ID_23946699,Human_RBP_ID_24381270,Human_RBP_ID_26501462,Human_RBP_ID_27307699 Human_Splice_Rec_2165100,Human_Splice_Rec_2165124,Human_Splice_Rec_2165148,Human_Splice_Rec_2165162,Human_Splice_Rec_2165170,Human_Splice_Rec_2165190,Human_Splice_Rec_2165216,Human_Splice_Rec_2165224,Human_Splice_Rec_2165238,Human_Splice_Rec_2165258,Human_Splice_Rec_2165278 Human_miRNA_ID_829710 RMVar_hsa_circ_54430,RMVar_hsa_circ_214226,RMVar_hsa_circ_78368,RMVar_hsa_circ_114469,RMVar_hsa_circ_214227,RMVar_hsa_circ_121650,RMVar_hsa_circ_267854,RMVar_hsa_circ_295967,RMVar_hsa_circ_62491,RMVar_hsa_circ_214231,RMVar_hsa_circ_112624,RMVar_hsa_circ_214228,RMVar_hsa_circ_214229,RMVar_hsa_circ_116130,RMVar_hsa_circ_355400,RMVar_hsa_circ_57498,RMVar_hsa_circ_214230 90343 RMVar_ID_90343 Human_SNP_ID_703581585 m1A Human chr22 - 37853310 37853310 37853310 AGCTTTTTAATAAACTTTCACTCCTGCTCTCAAACTTGCCTCCCTCTCTTCTTCTGCCTTGTGCC AGCTTTTTAATAAACTTTCACTCCTGCTCTCACACTTGCCTCCCTCTCTTCTTCTGCCTTGTGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37853306..37853430 26863196 MeRIP-seq:(Medium) rs1380628976 Functional Loss SNV dbSNP153 33..33 33 - - - 90344 RMVar_ID_90344 Human_SNP_ID_703581766 m1A Human chr22 + 37854108 37854108 37854108 TAGGAGAATGTGAGAAGAAATGCTGGTGCCTTAAGAAGTATGTTTCTTTAGGGATGGGTGGGCAG TAGGAGAATGTGAGAAGAAATGCTGGTGCCTTTAGAAGTATGTTTCTTTAGGGATGGGTGGGCAG A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37854104..37854235 26863196 MeRIP-seq:(Medium) rs1474751792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54430,RMVar_hsa_circ_214226,RMVar_hsa_circ_78368,RMVar_hsa_circ_114469,RMVar_hsa_circ_214227,RMVar_hsa_circ_121650,RMVar_hsa_circ_267854,RMVar_hsa_circ_62491,RMVar_hsa_circ_214231,RMVar_hsa_circ_214229,RMVar_hsa_circ_116130,RMVar_hsa_circ_355400,RMVar_hsa_circ_57498 90345 RMVar_ID_90345 Human_SNP_ID_703586532 m1A Human chr22 + 37870334 37870334 37870334 GACAAATCCAACATCAACCGACAGTTGGAGGTATACACAAGCGGAGGTGAGTGCAGCAGGCCGAC GACAAATCCAACATCAACCGACAGTTGGAGGTGTACACAAGCGGAGGTGAGTGCAGCAGGCCGAC A G EIF3L Ensembl:ENSG00000100129 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37870283..37886850 32194978 MeRIP-seq:(Medium) rs544036443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_282029,Human_RBP_ID_4696507,Human_RBP_ID_18194112,Human_RBP_ID_19113321,Human_RBP_ID_26822515 Human_Splice_Rec_2165111,Human_Splice_Rec_2165135,Human_Splice_Rec_2165165,Human_Splice_Rec_2165177,Human_Splice_Rec_2165201,Human_Splice_Rec_2165249,Human_Splice_Rec_2165267,Human_Splice_Rec_2165293,Human_Splice_Rec_2165295 Human_miRNA_ID_2363075,Human_miRNA_ID_3092178 RMVar_hsa_circ_11140,RMVar_hsa_circ_214226,RMVar_hsa_circ_78368,RMVar_hsa_circ_114469,RMVar_hsa_circ_214227,RMVar_hsa_circ_121650,RMVar_hsa_circ_62491,RMVar_hsa_circ_214231,RMVar_hsa_circ_214229,RMVar_hsa_circ_116130,RMVar_hsa_circ_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_11878,RMVar_hsa_circ_344193,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_65564,RMVar_hsa_circ_80513,RMVar_hsa_circ_214234,RMVar_hsa_circ_214233,RMVar_hsa_circ_214236,RMVar_hsa_circ_214239,RMVar_hsa_circ_116184,RMVar_hsa_circ_373817,RMVar_hsa_circ_313974,RMVar_hsa_circ_214238,RMVar_hsa_circ_303735,RMVar_hsa_circ_214241,RMVar_hsa_circ_8617,RMVar_hsa_circ_214240 90346 RMVar_ID_90346 Human_SNP_ID_703588737 m1A Human chr22 + 37877990 37877990 37877990 GGCCCAGCTTTCAACCATCCGCAGCTTCCTGAAGCTCTACACCACCATGCCTGTGGCCAAGCTGG GGCCCAGCTTTCAACCATCCGCAGCTTCCTGAGGCTCTACACCACCATGCCTGTGGCCAAGCTGG A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37877951..37878024 26863196 MeRIP-seq:(Medium) rs757960234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579749,Human_RBP_ID_1029296,Human_RBP_ID_1136848,Human_RBP_ID_1611219,Human_RBP_ID_1942598,Human_RBP_ID_3679510,Human_RBP_ID_5424483,Human_RBP_ID_5446524,Human_RBP_ID_5473126,Human_RBP_ID_5504775,Human_RBP_ID_5601670,Human_RBP_ID_8209075,Human_RBP_ID_8549864,Human_RBP_ID_17285927,Human_RBP_ID_17399827,Human_RBP_ID_17515115,Human_RBP_ID_18788744,Human_RBP_ID_22086985,Human_RBP_ID_26822524,Human_RBP_ID_27493805 RMVar_hsa_circ_78368,RMVar_hsa_circ_214227,RMVar_hsa_circ_62491,RMVar_hsa_circ_214231,RMVar_hsa_circ_116130,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_214233,RMVar_hsa_circ_214239,RMVar_hsa_circ_116184,RMVar_hsa_circ_303735,RMVar_hsa_circ_25643,RMVar_hsa_circ_214241,RMVar_hsa_circ_8617,RMVar_hsa_circ_293452,RMVar_hsa_circ_214243,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430,RMVar_hsa_circ_214244,RMVar_hsa_circ_272340,RMVar_hsa_circ_374484,RMVar_hsa_circ_214246 90347 RMVar_ID_90347 Human_SNP_ID_703591623 m1A Human chr22 + 37888532 37888525 37888533 TATTATAGGCAGGAAGTGTTTTTGCTACCGTGAAACCTTTACCTAGATCAGCCATCAGCCTGTCA TATTATAGGCAGGAAGTGTTTTTGCT________ACCTTTACCTAGATCAGCCATCAGCCTGTCA TACCGTGAA T AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37888482..37888583 26863196 MeRIP-seq:(Medium) rs560332770 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_579766,Human_RBP_ID_5101697,Human_RBP_ID_5205758,Human_RBP_ID_14479557,Human_RBP_ID_17286768,Human_RBP_ID_17515833,Human_RBP_ID_17989434,Human_RBP_ID_21896777,Human_RBP_ID_23212769 90348 RMVar_ID_90348 Human_SNP_ID_703593031 m1A Human chr22 + 37894039 37894039 37894039 AAGTGAGATGCCCAGTTCTCAGGCTGTCTGAGATGGGGGTTGGTGGCTGGAGCAGGTTTGGGACT AAGTGAGATGCCCAGTTCTCAGGCTGTCTGAGGTGGGGGTTGGTGGCTGGAGCAGGTTTGGGACT A G AL022311.1 Ensembl:ENSG00000279738 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37894000..37894135 26863196 MeRIP-seq:(Medium) rs1435085594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7080491,Human_RBP_ID_14479800,Human_RBP_ID_23946774 90349 RMVar_ID_90349 Human_SNP_ID_703595932 m1A Human chr22 - 37906290 37906290 37906290 CCGAGCTCGGGCGCCGACCGGCAGGCGAGGGGAGGGGCGGAGGCGGGGCCGCGGTGTCCTCGCTC CCGAGCTCGGGCGCCGACCGGCAGGCGAGGGGGGGGGCGGAGGCGGGGCCGCGGTGTCCTCGCTC T C RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:37906192..37906302 26863410 MeRIP-seq:(Medium) rs1000172999 Functional Loss SNV dbSNP153 33..33 33 - - - 90350 RMVar_ID_90350 Human_SNP_ID_703601354 m1A Human chr22 - 37925850 37925850 37925850 TCCTTGTCCTCCTCCTCCTCCTCAAAGGGGTTATAGGGTTTGGACTCCAGGCTGGCCGTTGGGCT TCCTTGTCCTCCTCCTCCTCCTCAAAGGGGTTCTAGGGTTTGGACTCCAGGCTGGCCGTTGGGCT T G RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37925810..37925974 26863196 MeRIP-seq:(Medium) rs1189764373 Functional Loss SNV dbSNP153 33..33 33 - - - 90351 RMVar_ID_90351 Human_SNP_ID_703601366 m1A Human chr22 + 37925876 37925874 37925877 ACCCTATAACCCCTTTGAGGAGGAGGAGGAGGACAAGGAGGAAGAGGCTCCAGCTGCACCCAGCC ACCCTATAACCCCTTTGAGGAGGAGGAGGAG___AAGGAGGAAGAGGCTCCAGCTGCACCCAGCC GGAC G MICALL1 Ensembl:ENSG00000100139 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37925835..37925976 26863196 MeRIP-seq:(Medium) rs1569143803 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4696631,Human_RBP_ID_18788763 RMVar_hsa_circ_99330,RMVar_hsa_circ_30695,RMVar_hsa_circ_120352,RMVar_hsa_circ_343954,RMVar_hsa_circ_124624,RMVar_hsa_circ_214248,RMVar_hsa_circ_115279,RMVar_hsa_circ_214252,RMVar_hsa_circ_214253,RMVar_hsa_circ_214251 90352 RMVar_ID_90352 Human_SNP_ID_703601368 m1A Human chr22 + 37925876 37925876 37925876 ACCCTATAACCCCTTTGAGGAGGAGGAGGAGGACAAGGAGGAAGAGGCTCCAGCTGCACCCAGCC ACCCTATAACCCCTTTGAGGAGGAGGAGGAGGTCAAGGAGGAAGAGGCTCCAGCTGCACCCAGCC A T MICALL1 Ensembl:ENSG00000100139 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37925835..37925976 26863196 MeRIP-seq:(Medium) rs1206590816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4696631,Human_RBP_ID_18788763 RMVar_hsa_circ_99330,RMVar_hsa_circ_30695,RMVar_hsa_circ_120352,RMVar_hsa_circ_343954,RMVar_hsa_circ_124624,RMVar_hsa_circ_214248,RMVar_hsa_circ_115279,RMVar_hsa_circ_214252,RMVar_hsa_circ_214253,RMVar_hsa_circ_214251 90353 RMVar_ID_90353 Human_SNP_ID_703601392 m1A Human chr22 - 37925975 37925958 37925975 GCTTCTTTGTCTTGGGGCTGCTGGTAGGGGTGATGCCGTACCAGGGGTGCAGGGACTTGGGTGTG GCTTCTTTGTCTTGGGGCTGCTGGTAGGGGTG_________________CAGGGACTTGGGTGTG GCACCCCTGGTACGGCAT G RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37925926..37926004 26863196 MeRIP-seq:(Medium) rs1174373336 Functional Loss DEL dbSNP153 33..49 33 - - - 90354 RMVar_ID_90354 Human_SNP_ID_703607494 m1A Human chr22 + 37947773 37947773 37947773 GTGATCCACCCACCTCGGCCTCCCAAAGTGCTAGGATTATAGGCATGAGCTATTGCACCTGGCCA GTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCTATTGCACCTGGCCA A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs929483505 Functional Loss SNV dbSNP153 33..33 33 - - - 90355 RMVar_ID_90355 Human_SNP_ID_703609164 m1A Human chr22 - 37953740 37953740 37953740 GCGACCCCGCTGCGCCCCGGTCCCGCGCGGAGACCCGCAAACAGCGACACTACGACTCGCGCGGC GCGACCCCGCTGCGCCCCGGTCCCGCGCGGAGCCCCGCAAACAGCGACACTACGACTCGCGCGGC T G RF00017-1361 RNACentral:URS000095F2A1 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37953676..37953969 26863196 MeRIP-seq:(Medium) rs1400064213 Functional Loss SNV dbSNP153 33..33 33 - - - 90356 RMVar_ID_90356 Human_SNP_ID_703609449 m1A Human chr22 + 37954768 37954762 37954768 GTGGGTGCAAAGAGAGCTAGTCTGAAGATAAAAATAAGAAACGTGTGGGATTGCTACCCCATTCC GTGGGTGCAAAGAGAGCTAGTCTGAAG______ATAAGAAACGTGTGGGATTGCTACCCCATTCC GATAAAA G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37954766..37955020 26863196 MeRIP-seq:(Medium) rs1193563109 Functional Loss DEL dbSNP153 28..33 33 - - - 90357 RMVar_ID_90357 Human_SNP_ID_703612558 m1A Human chr22 + 37967079 37967079 37967079 GCCCTTCTCCCTGGGTTTGTAGTCTCCCTAACACCTGTCCCTATCCCTACAGGATGTGTGCCCCT GCCCTTCTCCCTGGGTTTGTAGTCTCCCTAACGCCTGTCCCTATCCCTACAGGATGTGTGCCCCT A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37967076..37967175 32194978 MeRIP-seq:(Medium) rs772040079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22675292,Human_RBP_ID_22744751 Human_Splice_Rec_2165467,Human_Splice_Rec_2165479,Human_Splice_Rec_2165497,Human_Splice_Rec_2165505,Human_Splice_Rec_2165513,Human_Splice_Rec_2165521,Human_Splice_Rec_2165541,Human_Splice_Rec_2165547 90358 RMVar_ID_90358 Human_SNP_ID_703635142 m1A Human chr22 + 38057499 38057499 38057499 CGGCTGTGGGACCAACGCTTCCGGTGAGCGACAGAGGCAGCTCCCCAGGGCCTGGAGACCCGTGG CGGCTGTGGGACCAACGCTTCCGGTGAGCGACCGAGGCAGCTCCCCAGGGCCTGGAGACCCGTGG A C PICK1 Ensembl:ENSG00000100151 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38057450..38057531 26863196 MeRIP-seq:(Medium) rs1270653527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423744,Human_RBP_ID_18788820,Human_RBP_ID_19112077 Human_Splice_Rec_2165665,Human_Splice_Rec_2165679,Human_Splice_Rec_2165687,Human_Splice_Rec_2165711,Human_Splice_Rec_2165717 90359 RMVar_ID_90359 Human_SNP_ID_703636964 m1A Human chr22 - 38065105 38065105 38065105 CCCTTACCTTCACCTCCTGAATCATCTTCGCCACCTCCACCTTAGTTTTCCCTTTGATTGACCTG CCCTTACCTTCACCTCCTGAATCATCTTCGCCCCCTCCACCTTAGTTTTCCCTTTGATTGACCTG T G AL031587.2 Ensembl:ENSG00000233739 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38065054..38065193 26863196 MeRIP-seq:(Medium) rs908750329 Functional Loss SNV dbSNP153 33..33 33 - - - 90360 RMVar_ID_90360 Human_SNP_ID_703637408 m1A Human chr22 + 38067070 38067070 38067070 GGGGTGGAGGAGGGAATAATCAGTGTAGGGAAATGACACGGCAAAGGCTTGGAGTGTGGTTTGCG GGGGTGGAGGAGGGAATAATCAGTGTAGGGAAGTGACACGGCAAAGGCTTGGAGTGTGGTTTGCG A G PICK1 Ensembl:ENSG00000100151 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38067067..38067217 26863196 MeRIP-seq:(Medium) rs1328982337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376697 90361 RMVar_ID_90361 Human_SNP_ID_703644105 m1A Human chr22 + 38087214 38087206 38087215 AGGTCATGGGGGTCACGGGGGTCATGGGATTCACGGGCCCCTCCTCCAGAGCCTTCACGTACGCC AGGTCATGGGGGTCACGGGGGTCAT_________GGGCCCCTCCTCCAGAGCCTTCACGTACGCC TGGGATTCAC T NONHSAG033903.2,NONHSAG033903.2:2,NONHSAG033903.2:3,NONHSAG033903.2:4,NONHSAG033903.2:5,NONHSAG033903.2:6 RNACentral:URS00008C2CBB,RNACentral:URS00008C2DF3,RNACentral:URS00009B4F9A,RNACentral:URS00008B4DB3,RNACentral:URS00009C14A7,RNACentral:URS00008C236A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38087212..38087281 26863196 MeRIP-seq:(Medium) rs751428030 Functional Loss DEL dbSNP153 26..34 33 - - - 90362 RMVar_ID_90362 Human_SNP_ID_703644728 m1A Human chr22 + 38088871 38088871 38088871 GCGTGTGGTTGGCGCCCTCCGAGTGGGAGACCAGGGCGCGGACTCTCCTGGCGCCCCCGCCGCCG GCGTGTGGTTGGCGCCCTCCGAGTGGGAGACCCGGGCGCGGACTCTCCTGGCGCCCCCGCCGCCG A C NONHSAG033903.2,NONHSAG033903.2:2,NONHSAG033903.2:3,NONHSAG033903.2:4,NONHSAG033903.2:5 RNACentral:URS00008C2CBB,RNACentral:URS00008C2DF3,RNACentral:URS00008C1439,RNACentral:URS00009C14A7,RNACentral:URS00008C236A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38088862..38088962 26863196 MeRIP-seq:(Medium) rs1488787780 Functional Loss SNV dbSNP153 33..33 33 - - - 90363 RMVar_ID_90363 Human_SNP_ID_703644868 m1A Human chr22 + 38089144 38089121 38089144 GGGCAGGGAGCGACGGTCTGGCTCTAGCTGGGACGCGGGCCTCGCGTCGGGCTCGGTGCCGTAGG GGGCAGGGAG_______________________CGCGGGCCTCGCGTCGGGCTCGGTGCCGTAGG GCGACGGTCTGGCTCTAGCTGGGA G NONHSAG033903.2 RNACentral:URS00008C2CBB lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38089136..38089238 26863196 MeRIP-seq:(Medium) rs1458139372 Functional Loss DEL dbSNP153 11..33 33 - - - 90364 RMVar_ID_90364 Human_SNP_ID_703645033 m1A Human chr22 + 38089371 38089371 38089371 GGGGCGGAGACCGGGCCACCACGGGGGCGCGGAGAACGCGCCGGGGCGGAAGGGCAGGCCGGGGG GGGGCGGAGACCGGGCCACCACGGGGGCGCGGGGAACGCGCCGGGGCGGAAGGGCAGGCCGGGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38089320..38089589 26863196 MeRIP-seq:(Medium) rs1208045546 Functional Loss SNV dbSNP153 33..33 33 - - - 90365 RMVar_ID_90365 Human_SNP_ID_703645130 m1A Human chr22 + 38089571 38089571 38089571 GCGTCAGGCGGCCCGAGGGGTAGGGCGGCCCCAGCGCGGGGCCCAGCAGGCCGGGGGAGTGGGCG GCGTCAGGCGGCCCGAGGGGTAGGGCGGCCCCGGCGCGGGGCCCAGCAGGCCGGGGGAGTGGGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38089526..38089938 26863196 MeRIP-seq:(Medium) rs960726795 Functional Loss SNV dbSNP153 33..33 33 - - - 90366 RMVar_ID_90366 Human_SNP_ID_703675908 m1A Human chr22 + 38202158 38202158 38202158 TGACCGGAGCGCGGATCGGGACAGCGGCCGGGACAGCGGCGAGACGCGCGTGTGTGAGCGCGCCG TGACCGGAGCGCGGATCGGGACAGCGGCCGGGGCAGCGGCGAGACGCGCGTGTGTGAGCGCGCCG A G MAFF Ensembl:ENSG00000185022 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38202066..38202494 26863196 MeRIP-seq:(Medium) rs1484386991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709042,Human_RBP_ID_18423645,Human_RBP_ID_26345979 Human_Splice_Rec_2166435,Human_Splice_Rec_2166437,Human_Splice_Rec_2166441,Human_Splice_Rec_2166445 90367 RMVar_ID_90367 Human_SNP_ID_703676518 m1A Human chr22 + 38204848 38204848 38204848 ACTGTGTTGGCTTGCGGGGAGGCTGGCATTGCAGGGTTTTGAAATGGGCCAAGCACGGACAGGCT ACTGTGTTGGCTTGCGGGGAGGCTGGCATTGCGGGGTTTTGAAATGGGCCAAGCACGGACAGGCT A G MAFF Ensembl:ENSG00000185022 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38204846..38205003 26863196 MeRIP-seq:(Medium) rs1355106321 Functional Loss SNV dbSNP153 33..33 33 - - - 90368 RMVar_ID_90368 Human_SNP_ID_703679338 m1A Human chr22 + 38215369 38215368 38215370 TTGGGCCTGGGGGTGCCTGGCCTTCCGAAACTAAAAGAGTGGGTGGGAAGACTAGTGAAACCCAG TTGGGCCTGGGGGTGCCTGGCCTTCCGAAACT__AAGAGTGGGTGGGAAGACTAGTGAAACCCAG TAA T MAFF Ensembl:ENSG00000185022 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38215318..38215468 32194978 MeRIP-seq:(Medium) rs1400644604 Functional Loss DEL dbSNP153 33..34 33 - - - 90369 RMVar_ID_90369 Human_SNP_ID_703680596 m1A Human chr22 + 38219747 38219745 38219747 TTGGCCTGGAGGGAGAAGGGAAGCCACGGTGGAGAGACAGCTTGGTGAAAGCAGATGGCGGGGCA TTGGCCTGGAGGGAGAAGGGAAGCCACGGTG__GAGACAGCTTGGTGAAAGCAGATGGCGGGGCA GGA G lnc-MAFF-2 RNACentral:URS00008B5FF0 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38219589..38220138 32194978 MeRIP-seq:(Medium) rs761260041 Functional Loss DEL dbSNP153 32..33 33 - - - 90370 RMVar_ID_90370 Human_SNP_ID_703680981 m1A Human chr22 + 38221085 38221082 38221085 TGCACGGTGTGTGGGGGAGCCACGGCTTGCCGACCTCAGCCTGAGAGTCTCGCGGGGAGGAGGGG TGCACGGTGTGTGGGGGAGCCACGGCTTGC___CCTCAGCCTGAGAGTCTCGCGGGGAGGAGGGG CCGA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38221035..38221285 32194978 MeRIP-seq:(Medium) rs1440730164 Functional Loss DEL dbSNP153 31..33 33 - - - 90371 RMVar_ID_90371 Human_SNP_ID_703685325 m1A Human chr22 - 38237005 38237005 38237005 AGGAAAGAAGGCCATTCAGAAGAAGCCAGTAGAGGAGAGGTCAGAAGCAGCATTTGGGAGGGCGA AGGAAAGAAGGCCATTCAGAAGAAGCCAGTAGTGGAGAGGTCAGAAGCAGCATTTGGGAGGGCGA T A TMEM184B Ensembl:ENSG00000198792 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38237003..38237086 26863196 MeRIP-seq:(Medium) rs1327356471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41314,RMVar_hsa_circ_214270,RMVar_hsa_circ_314687,RMVar_hsa_circ_318579,RMVar_hsa_circ_214271,RMVar_hsa_circ_214272,RMVar_hsa_circ_341070 90372 RMVar_ID_90372 Human_SNP_ID_703688202 m1A Human chr22 - 38247832 38247832 38247832 CTGCCATGGAGCAGCCTGTGTTCCTGATGACAACTGCCGCTCAGGCCATCTCTGGCTTCTTCGTG CTGCCATGGAGCAGCCTGTGTTCCTGATGACAGCTGCCGCTCAGGCCATCTCTGGCTTCTTCGTG T C TMEM184B Ensembl:ENSG00000198792 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:38247709..38247925 26863196 MeRIP-seq:(Medium) rs763261821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2166461,Human_Splice_Rec_2166477,Human_Splice_Rec_2166495,Human_Splice_Rec_2166551,Human_Splice_Rec_2166557,Human_Splice_Rec_2166565 RMVar_hsa_circ_41314,RMVar_hsa_circ_318579,RMVar_hsa_circ_214271,RMVar_hsa_circ_214272,RMVar_hsa_circ_341070,RMVar_hsa_circ_280465,RMVar_hsa_circ_214274,RMVar_hsa_circ_214275,RMVar_hsa_circ_319660 90373 RMVar_ID_90373 Human_SNP_ID_703688250 m1A Human chr22 + 38247922 38247922 38247922 GACGCTGGGCGAGGCTGCTGCGGTCGTGGGCGACGCTGGATCCGGGGCCAGCACATCCCCCCTCA GACGCTGGGCGAGGCTGCTGCGGTCGTGGGCGGCGCTGGATCCGGGGCCAGCACATCCCCCCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38247819..38248036 26863196 MeRIP-seq:(Medium) rs1487005037 Functional Loss SNV dbSNP153 33..33 33 - - - 90374 RMVar_ID_90374 Human_SNP_ID_703688282 m1A Human chr22 - 38247986 38247986 38247986 CTAGCTTGTCACTTTCTGCAAAGGTTTCCCTCAGGGAGCCTCCTGCTGCCAGGCACCATGACAGT CTAGCTTGTCACTTTCTGCAAAGGTTTCCCTCGGGGAGCCTCCTGCTGCCAGGCACCATGACAGT T C TMEM184B Ensembl:ENSG00000198792 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38247936..38273000 26863196 MeRIP-seq:(Medium) rs199536196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153539,Human_RBP_ID_4696981,Human_RBP_ID_17285949,Human_RBP_ID_22269816 Human_Splice_Rec_2166460,Human_Splice_Rec_2166476,Human_Splice_Rec_2166494,Human_Splice_Rec_2166550,Human_Splice_Rec_2166556,Human_Splice_Rec_2166564 Human_miRNA_ID_1974039,Human_miRNA_ID_1976219,Human_miRNA_ID_2224459,Human_miRNA_ID_2487534,Human_miRNA_ID_2614007,Human_miRNA_ID_3002366,Human_miRNA_ID_3075901 RMVar_hsa_circ_41314,RMVar_hsa_circ_318579,RMVar_hsa_circ_214271,RMVar_hsa_circ_214272,RMVar_hsa_circ_341070,RMVar_hsa_circ_280465,RMVar_hsa_circ_214274,RMVar_hsa_circ_214275,RMVar_hsa_circ_319660 90375 RMVar_ID_90375 Human_SNP_ID_703694490 m1A Human chr22 - 38272741 38272741 38272741 CCGCCGGCTCCCGGGCGGGGAGGGCACTACGGAGGCCGGTGCGGCCGCGGAGGGAGGGGGCATCC CCGCCGGCTCCCGGGCGGGGAGGGCACTACGGGGGCCGGTGCGGCCGCGGAGGGAGGGGGCATCC T C TMEM184B Ensembl:ENSG00000198792 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38272737..38272857 32194978 MeRIP-seq:(Medium) rs1416555746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3676769,Human_RBP_ID_26789569 90376 RMVar_ID_90376 Human_SNP_ID_703694537 m1A Human chr22 + 38272839 38272839 38272839 GAAACAAGCAGCCCCCCGCGCTCGGGAGTCGCAGCTCCCCCTTGGGGCTCCCGGGCGAGGCCGGC GAAACAAGCAGCCCCCCGCGCTCGGGAGTCGCTGCTCCCCCTTGGGGCTCCCGGGCGAGGCCGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38272835..38272975 26863196 MeRIP-seq:(Medium) rs930661800 Functional Loss SNV dbSNP153 33..33 33 - - - 90377 RMVar_ID_90377 Human_SNP_ID_703700125 m1A Human chr22 - 38291992 38291990 38291992 ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAGTAGCCAGAGACAGCTGTGTACCTCACCTGT ACAGAGCGAGACTCCATCTCAAAAAAAAAAAA__GTAGCCAGAGACAGCTGTGTACCTCACCTGT CTT C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs549849173 Functional Loss DEL dbSNP153 33..34 33 - - - 90378 RMVar_ID_90378 Human_SNP_ID_703700126 m1A Human chr22 - 38291992 38291990 38291992 ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAGTAGCCAGAGACAGCTGTGTACCTCACCTGT ACAGAGCGAGACTCCATCTCAAAAAAAAAAAA_AGTAGCCAGAGACAGCTGTGTACCTCACCTGT CTT CT TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs549849173 Functional Loss DEL dbSNP153 33..33 33 - - - 90379 RMVar_ID_90379 Human_SNP_ID_703700130 m1A Human chr22 - 38291992 38291992 38291992 ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAGTAGCCAGAGACAGCTGTGTACCTCACCTGT ACAGAGCGAGACTCCATCTCAAAAAAAAAAAATAGTAGCCAGAGACAGCTGTGTACCTCACCTGT T A TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1348856800 Functional Loss SNV dbSNP153 33..33 33 - - - 90380 RMVar_ID_90380 Human_SNP_ID_703700131 m1A Human chr22 - 38291992 38291992 38291992 ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAGTAGCCAGAGACAGCTGTGTACCTCACCTGT ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAGAGTAGCCAGAGACAGCTGTGTACCTCACCTGT T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1348856800 Functional Loss SNV dbSNP153 33..33 33 - - - 90381 RMVar_ID_90381 Human_SNP_ID_703700770 m1A Human chr22 + 38294178 38294178 38294178 GTGAGGTCTGAGGAGGAGACGTTGGCGGGCGCACCCCTGTGCAGCCTCATACTCACCTTCCTCTC GTGAGGTCTGAGGAGGAGACGTTGGCGGGCGCGCCCCTGTGCAGCCTCATACTCACCTTCCTCTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:38294176..38294225 26863196 MeRIP-seq:(Medium) rs1268813746 Functional Loss SNV dbSNP153 33..33 33 - - - 90382 RMVar_ID_90382 Human_SNP_ID_703700870 m1A Human chr22 - 38294393 38294393 38294393 CACCCACGGGGGCCACTGCCAACCGGCTCCGCAGTGCCGCCGAGCCCGTGGCTTCCACGCCAGCC CACCCACGGGGGCCACTGCCAACCGGCTCCGCGGTGCCGCCGAGCCCGTGGCTTCCACGCCAGCC T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38294259..38294423 26863196 MeRIP-seq:(Medium) rs369141815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580035,Human_RBP_ID_4712375,Human_RBP_ID_18194120,Human_RBP_ID_18445453,Human_RBP_ID_19008050 Human_Splice_Rec_2166583,Human_Splice_Rec_2166603,Human_Splice_Rec_2166609,Human_Splice_Rec_2166617,Human_Splice_Rec_2166623,Human_Splice_Rec_2166641,Human_Splice_Rec_2166653,Human_Splice_Rec_2166657,Human_Splice_Rec_2166743 Human_miRNA_ID_2018152 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_378565,RMVar_hsa_circ_58767,RMVar_hsa_circ_214277 90383 RMVar_ID_90383 Human_SNP_ID_703700883 m1A Human chr22 - 38294424 38294424 38294424 GGGTCCGCGACCCGAGCCCTGCCCCCTGGCCCACCCACGGGGGCCACTGCCAACCGGCTCCGCAG GGGTCCGCGACCCGAGCCCTGCCCCCTGGCCCGCCCACGGGGGCCACTGCCAACCGGCTCCGCAG T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38294377..38294475 26863196 MeRIP-seq:(Medium) rs1404977638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580036,Human_RBP_ID_18194120,Human_RBP_ID_24494075 Human_Splice_Rec_2166583,Human_Splice_Rec_2166603,Human_Splice_Rec_2166609,Human_Splice_Rec_2166617,Human_Splice_Rec_2166623,Human_Splice_Rec_2166641,Human_Splice_Rec_2166653,Human_Splice_Rec_2166657,Human_Splice_Rec_2166743 Human_miRNA_ID_2458602,Human_miRNA_ID_2463525,Human_miRNA_ID_2636166,Human_miRNA_ID_2638853,Human_miRNA_ID_2663929,Human_miRNA_ID_2682388,Human_miRNA_ID_2874433,Human_miRNA_ID_2982393 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_378565,RMVar_hsa_circ_58767,RMVar_hsa_circ_214277 90384 RMVar_ID_90384 Human_SNP_ID_703702115 m1A Human chr22 - 38298725 38298723 38298725 TGGGGGACTGGATGGGGAAGGCCCTGACTCAGAGGGCCAGAGTGAGCTGGTGGCGGGAGGGGCTC TGGGGGACTGGATGGGGAAGGCCCTGACTCAG__GGCCAGAGTGAGCTGGTGGCGGGAGGGGCTC CCT C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38298719..38298886 26863196 MeRIP-seq:(Medium) rs1280939918 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_65743,Human_RBP_ID_930982,Human_RBP_ID_3677580,Human_RBP_ID_5387380,Human_RBP_ID_9126440,Human_RBP_ID_22362530,Human_RBP_ID_22675305,Human_RBP_ID_22725142,Human_RBP_ID_23015987,Human_RBP_ID_26345415,Human_RBP_ID_26789358,Human_RBP_ID_27037365,Human_RBP_ID_27821305,Human_RBP_ID_27841117 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542 90385 RMVar_ID_90385 Human_SNP_ID_703702116 m1A Human chr22 - 38298725 38298725 38298725 TGGGGGACTGGATGGGGAAGGCCCTGACTCAGAGGGCCAGAGTGAGCTGGTGGCGGGAGGGGCTC TGGGGGACTGGATGGGGAAGGCCCTGACTCAGGGGGCCAGAGTGAGCTGGTGGCGGGAGGGGCTC T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38298719..38298886 26863196 MeRIP-seq:(Medium) rs557713848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65743,Human_RBP_ID_930982,Human_RBP_ID_3677580,Human_RBP_ID_5387380,Human_RBP_ID_9126440,Human_RBP_ID_22362530,Human_RBP_ID_22675305,Human_RBP_ID_22725142,Human_RBP_ID_23015987,Human_RBP_ID_26345415,Human_RBP_ID_26789358,Human_RBP_ID_27037365,Human_RBP_ID_27821305,Human_RBP_ID_27841117 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542 90386 RMVar_ID_90386 Human_SNP_ID_703706402 m1A Human chr22 - 38314167 38314167 38314167 CTGACCCTCATGTTCCTGCTTCCTCTGCAGCAAGAGTGAGCCATGGAGCTACGTGTGGGGAACAA CTGACCCTCATGTTCCTGCTTCCTCTGCAGCAGGAGTGAGCCATGGAGCTACGTGTGGGGAACAA T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:38314126..38314175 26863196 MeRIP-seq:(Medium) rs748049706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65754,Human_RBP_ID_780917,Human_RBP_ID_19008055,Human_RBP_ID_27821309 Human_Splice_Rec_2166570,Human_Splice_Rec_2166571,Human_Splice_Rec_2166590,Human_Splice_Rec_2166591,Human_Splice_Rec_2166628,Human_Splice_Rec_2166629,Human_Splice_Rec_2166660,Human_Splice_Rec_2166661,Human_Splice_Rec_2166674,Human_Splice_Rec_2166675,Human_Splice_Rec_2166712,Human_Splice_Rec_2166713,Human_Splice_Rec_2166730,Human_Splice_Rec_2166731 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_302161,RMVar_hsa_circ_214280,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_89418,RMVar_hsa_circ_374717,RMVar_hsa_circ_125726,RMVar_hsa_circ_214286,RMVar_hsa_circ_214287,RMVar_hsa_circ_214292,RMVar_hsa_circ_214290,RMVar_hsa_circ_347070 90387 RMVar_ID_90387 Human_SNP_ID_703706403 m1A Human chr22 - 38314168 38314168 38314168 GCTGACCCTCATGTTCCTGCTTCCTCTGCAGCAAGAGTGAGCCATGGAGCTACGTGTGGGGAACA GCTGACCCTCATGTTCCTGCTTCCTCTGCAGCTAGAGTGAGCCATGGAGCTACGTGTGGGGAACA T A TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:38314154..38314244 26863410 MeRIP-seq:(Medium) rs201363944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65754,Human_RBP_ID_780917,Human_RBP_ID_19008055 Human_Splice_Rec_2166570,Human_Splice_Rec_2166571,Human_Splice_Rec_2166590,Human_Splice_Rec_2166591,Human_Splice_Rec_2166628,Human_Splice_Rec_2166629,Human_Splice_Rec_2166660,Human_Splice_Rec_2166661,Human_Splice_Rec_2166674,Human_Splice_Rec_2166675,Human_Splice_Rec_2166712,Human_Splice_Rec_2166713,Human_Splice_Rec_2166730,Human_Splice_Rec_2166731 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_302161,RMVar_hsa_circ_214280,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_89418,RMVar_hsa_circ_374717,RMVar_hsa_circ_125726,RMVar_hsa_circ_214286,RMVar_hsa_circ_214287,RMVar_hsa_circ_214292,RMVar_hsa_circ_214290,RMVar_hsa_circ_347070 90388 RMVar_ID_90388 Human_SNP_ID_703707438 m1A Human chr22 - 38317311 38317311 38317311 CCCAGAGCCAGAGCCCGGCCGGGGCCGAGCGGAGCGCGGCGGCGGCGGCGGCGGCGGCGGCTGGG CCCAGAGCCAGAGCCCGGCCGGGGCCGAGCGGCGCGCGGCGGCGGCGGCGGCGGCGGCGGCTGGG T G TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,Starvation treatment chr22:38317113..38317425;chr22:38317164..38317425;chr22:38317151..38317425 26863196,26863410,26863410 MeRIP-seq:(Medium) rs1284686495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930991,Human_RBP_ID_3678473,Human_RBP_ID_3962390,Human_RBP_ID_4708222,Human_RBP_ID_5240859,Human_RBP_ID_5529936,Human_RBP_ID_9333375,Human_RBP_ID_9433214,Human_RBP_ID_17671029,Human_RBP_ID_18423646,Human_RBP_ID_19008056,Human_RBP_ID_22454672,Human_RBP_ID_24561117,Human_RBP_ID_27821311 RMVar_hsa_circ_13824,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 90389 RMVar_ID_90389 Human_SNP_ID_703707444 m1A Human chr22 - 38317334 38317328 38317334 GGCGGCGGCGGCGGCGGCGAGAGCCCAGAGCCAGAGCCCGGCCGGGGCCGAGCGGAGCGCGGCGG GGCGGCGGCGGCGGCGGCGAGAGCCCAGAGCC______CGGCCGGGGCCGAGCGGAGCGCGGCGG GGGCTCT G TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr22:38317201..38317438 26863410 MeRIP-seq:(Medium) rs1478265548 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_211052,Human_RBP_ID_246357,Human_RBP_ID_929892,Human_RBP_ID_3676776,Human_RBP_ID_3962390,Human_RBP_ID_4708222,Human_RBP_ID_5529936,Human_RBP_ID_9332849,Human_RBP_ID_9433214,Human_RBP_ID_17671029,Human_RBP_ID_18194123,Human_RBP_ID_18423646,Human_RBP_ID_19008056,Human_RBP_ID_22454672,Human_RBP_ID_24561117,Human_RBP_ID_26345420,Human_RBP_ID_27821311 RMVar_hsa_circ_13824,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 90390 RMVar_ID_90390 Human_SNP_ID_703707496 m1A Human chr22 - 38317380 38317380 38317380 GGGGGCGGGCGGGCGGGCAGGAGGCCGGGAGGAGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG GGGGGCGGGCGGGCGGGCAGGAGGCCGGGAGGGGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:38317121..38317400 26863196 MeRIP-seq:(Medium) rs1419400507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65760,Human_RBP_ID_211052,Human_RBP_ID_834158,Human_RBP_ID_929892,Human_RBP_ID_1068909,Human_RBP_ID_3676776,Human_RBP_ID_3962390,Human_RBP_ID_4697206,Human_RBP_ID_5149019,Human_RBP_ID_5529936,Human_RBP_ID_8235509,Human_RBP_ID_9332849,Human_RBP_ID_9433214,Human_RBP_ID_17671029,Human_RBP_ID_18194123,Human_RBP_ID_18423646,Human_RBP_ID_18952615,Human_RBP_ID_19008056,Human_RBP_ID_22454672,Human_RBP_ID_24561117,Human_RBP_ID_26345420,Human_RBP_ID_26789806,Human_RBP_ID_27821311 RMVar_hsa_circ_13824,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 90391 RMVar_ID_90391 Human_SNP_ID_703707497 m1A Human chr22 - 38317380 38317380 38317380 GGGGGCGGGCGGGCGGGCAGGAGGCCGGGAGGAGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG GGGGGCGGGCGGGCGGGCAGGAGGCCGGGAGGCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCG T G TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:38317121..38317400 26863196 MeRIP-seq:(Medium) rs1419400507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65760,Human_RBP_ID_211052,Human_RBP_ID_834158,Human_RBP_ID_929892,Human_RBP_ID_1068909,Human_RBP_ID_3676776,Human_RBP_ID_3962390,Human_RBP_ID_4697206,Human_RBP_ID_5149019,Human_RBP_ID_5529936,Human_RBP_ID_8235509,Human_RBP_ID_9332849,Human_RBP_ID_9433214,Human_RBP_ID_17671029,Human_RBP_ID_18194123,Human_RBP_ID_18423646,Human_RBP_ID_18952615,Human_RBP_ID_19008056,Human_RBP_ID_22454672,Human_RBP_ID_24561117,Human_RBP_ID_26345420,Human_RBP_ID_26789806,Human_RBP_ID_27821311 RMVar_hsa_circ_13824,RMVar_hsa_circ_214278,RMVar_hsa_circ_105866,RMVar_hsa_circ_77501,RMVar_hsa_circ_214279,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 90392 RMVar_ID_90392 Human_SNP_ID_703728319 m1A Human chr22 - 38398781 38398781 38398781 CCCCCCCGCGCCTGCACTTAGCCCCGCGCCCGAGGTGAGCCCGGCCCCTAAATCCTCCGGGCGGG CCCCCCCGCGCCTGCACTTAGCCCCGCGCCCGCGGTGAGCCCGGCCCCTAAATCCTCCGGGCGGG T G TPTEP2 Ensembl:ENSG00000244627 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:38398776..38398900 26863410 MeRIP-seq:(Medium) rs1343174053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931452,Human_RBP_ID_4708636,Human_RBP_ID_7081364,Human_RBP_ID_19112106 Human_Splice_Rec_2166749,Human_Splice_Rec_2166767,Human_Splice_Rec_2166775,Human_Splice_Rec_2166785,Human_Splice_Rec_2166803,Human_Splice_Rec_2166821,Human_Splice_Rec_2166829 90393 RMVar_ID_90393 Human_SNP_ID_703728341 m1A Human chr22 - 38398815 38398815 38398815 GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGACCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGTCCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC T A TPTEP2 Ensembl:ENSG00000244627 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38398783..38398862 26863196 MeRIP-seq:(Medium) rs1027792000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423647,Human_RBP_ID_22270026 Human_Splice_Rec_2166749,Human_Splice_Rec_2166767,Human_Splice_Rec_2166775,Human_Splice_Rec_2166785,Human_Splice_Rec_2166803,Human_Splice_Rec_2166821,Human_Splice_Rec_2166829 90394 RMVar_ID_90394 Human_SNP_ID_703728342 m1A Human chr22 - 38398815 38398815 38398815 GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGACCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGCCCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC T G TPTEP2 Ensembl:ENSG00000244627 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38398783..38398862 26863196 MeRIP-seq:(Medium) rs1027792000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423647,Human_RBP_ID_22270026 Human_Splice_Rec_2166749,Human_Splice_Rec_2166767,Human_Splice_Rec_2166775,Human_Splice_Rec_2166785,Human_Splice_Rec_2166803,Human_Splice_Rec_2166821,Human_Splice_Rec_2166829 90395 RMVar_ID_90395 Human_SNP_ID_703728351 m1A Human chr22 + 38398829 38398829 38398829 GTGCAGGCGCGGGGGGGGTCCCTAGAGCCGCCAGGGCGCGGCGCGTCCGGCGCTGGGGGACTGTT GTGCAGGCGCGGGGGGGGTCCCTAGAGCCGCCGGGGCGCGGCGCGTCCGGCGCTGGGGGACTGTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:38398671..38398891;chr22:38398714..38398858;chr22:38398765..38398890 26863196 MeRIP-seq:(Medium) rs2413532 Functional Loss SNV dbSNP153 33..33 33 - - - 90396 RMVar_ID_90396 Human_SNP_ID_703728364 m1A Human chr22 - 38398850 38398850 38398850 TCCCTGAACACTTTCTGACCCAACAGTCCCCCAGCGCCGGACGCGCCGCGCCCTGGCGGCTCTAG TCCCTGAACACTTTCTGACCCAACAGTCCCCCGGCGCCGGACGCGCCGCGCCCTGGCGGCTCTAG T C TPTEP2 Ensembl:ENSG00000244627 Pseudogene exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38398667..38398893 26863196 MeRIP-seq:(Medium) rs1238667676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4697218,Human_RBP_ID_18423647 Human_Splice_Rec_2166749,Human_Splice_Rec_2166767,Human_Splice_Rec_2166775,Human_Splice_Rec_2166785,Human_Splice_Rec_2166803,Human_Splice_Rec_2166821,Human_Splice_Rec_2166829 90397 RMVar_ID_90397 Human_SNP_ID_703746735 m1A Human chr22 + 38468123 38468123 38468123 CGGGTGCGATCGCGGAGCTGTGAGGCGCAGGCAGGGCTCTGGGGCACCTAGAGACCGGGGCCGGA CGGGTGCGATCGCGGAGCTGTGAGGCGCAGGCTGGGCTCTGGGGCACCTAGAGACCGGGGCCGGA A T KDELR3 Ensembl:ENSG00000100196 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:38468051..38468260;chr22:38468076..38468225 26863196 MeRIP-seq:(Medium) rs944393342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708223,Human_RBP_ID_5240860,Human_RBP_ID_5324780,Human_RBP_ID_22086992,Human_RBP_ID_22454986 90398 RMVar_ID_90398 Human_SNP_ID_703748540 m1A Human chr22 - 38474484 38474484 38474484 CCAAGGGTAGACAGGAGACAATGAGGACACAGACTCCCAAGCCTGCCCACCCTCAAGAGGTGCAC CCAAGGGTAGACAGGAGACAATGAGGACACAGGCTCCCAAGCCTGCCCACCCTCAAGAGGTGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38474480..38474549 26863196 MeRIP-seq:(Medium) rs933453370 Functional Loss SNV dbSNP153 33..33 33 - - - 90399 RMVar_ID_90399 Human_SNP_ID_703751707 m1A Human chr22 - 38484336 38484336 38484336 CAATGTGCAACATACAGGTAGGTCTTCAGCATAAGCTGAAATATATGCATGTAAAAACTTTGACA CAATGTGCAACATACAGGTAGGTCTTCAGCATGAGCTGAAATATATGCATGTAAAAACTTTGACA T C DDX17 Ensembl:ENSG00000100201 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38484039..38484339 32194978 MeRIP-seq:(Medium) rs567588807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580170,Human_RBP_ID_1611569,Human_RBP_ID_1942773,Human_RBP_ID_2728343,Human_RBP_ID_5203372,Human_RBP_ID_7081462,Human_RBP_ID_8863583,Human_RBP_ID_9126489,Human_RBP_ID_14485456,Human_RBP_ID_17285986,Human_RBP_ID_17399170,Human_RBP_ID_17515178,Human_RBP_ID_18329255,Human_RBP_ID_18789085,Human_RBP_ID_20762109,Human_RBP_ID_22820613,Human_RBP_ID_23013170,Human_RBP_ID_23947449,Human_RBP_ID_27037572,Human_RBP_ID_27496092,Human_RBP_ID_27708383 Human_miRNA_ID_575816,Human_miRNA_ID_2205633,Human_miRNA_ID_2633534,Human_miRNA_ID_2929369 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_101987,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_214294 90400 RMVar_ID_90400 Human_SNP_ID_703752264 m1A Human chr22 + 38486008 38486008 38486008 ATTGGTAGGCAGTCTGCCCCATGTAACCTATCATATTGGTAGCTCCCGGAGGCTGTGCAAACTGT ATTGGTAGGCAGTCTGCCCCATGTAACCTATCGTATTGGTAGCTCCCGGAGGCTGTGCAAACTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38485957..38486120 26863196 MeRIP-seq:(Medium) rs958047393 Functional Loss SNV dbSNP153 33..33 33 - - - 90401 RMVar_ID_90401 Human_SNP_ID_703752281 m1A Human chr22 + 38486072 38486072 38486072 TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGACCGGCCTATCCCACTAAACTGCTGGCTAGAGC TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGCCCGGCCTATCCCACTAAACTGCTGGCTAGAGC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:38485926..38486100 26863196 MeRIP-seq:(Medium) rs1391153288 Functional Loss SNV dbSNP153 33..33 33 - - - 90402 RMVar_ID_90402 Human_SNP_ID_703752282 m1A Human chr22 + 38486072 38486072 38486072 TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGACCGGCCTATCCCACTAAACTGCTGGCTAGAGC TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGGCCGGCCTATCCCACTAAACTGCTGGCTAGAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:38485926..38486100 26863196 MeRIP-seq:(Medium) rs1391153288 Functional Loss SNV dbSNP153 33..33 33 - - - 90403 RMVar_ID_90403 Human_SNP_ID_703752369 m1A Human chr22 - 38486314 38486314 38486314 TGGTGGCCGGAGAGACTCTGCAAGCTATCGGGATCGTAGTGAAACCGATAGAGCTGGTTATGCTA TGGTGGCCGGAGAGACTCTGCAAGCTATCGGGCTCGTAGTGAAACCGATAGAGCTGGTTATGCTA T G DDX17 Ensembl:ENSG00000100201 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38486266..38486443 26863196 MeRIP-seq:(Medium) rs1176378055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245817,Human_RBP_ID_580240,Human_RBP_ID_931866,Human_RBP_ID_1611604,Human_RBP_ID_1942811,Human_RBP_ID_3672803,Human_RBP_ID_5599438,Human_RBP_ID_7081627,Human_RBP_ID_8863599,Human_RBP_ID_9126531,Human_RBP_ID_9392967,Human_RBP_ID_14485581,Human_RBP_ID_18445462,Human_RBP_ID_18789117,Human_RBP_ID_19009213,Human_RBP_ID_22086552,Human_RBP_ID_22820675,Human_RBP_ID_23013248,Human_RBP_ID_23947501,Human_RBP_ID_26345422,Human_RBP_ID_27037602 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_101987,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_214294 90404 RMVar_ID_90404 Human_SNP_ID_703752834 m1A Human chr22 - 38487970 38487970 38487970 TTCTTCACCCCAGGGAACCTAAAACAGGCCAGAGAGCTTATCAAAGTGCTGGAAGAGGCCAATCA TTCTTCACCCCAGGGAACCTAAAACAGGCCAGGGAGCTTATCAAAGTGCTGGAAGAGGCCAATCA T C DDX17 Ensembl:ENSG00000100201 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38487919..38488100 32194978 MeRIP-seq:(Medium) rs1339943006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833555,Human_RBP_ID_1611618,Human_RBP_ID_1942814,Human_RBP_ID_3672806,Human_RBP_ID_7081651,Human_RBP_ID_8550250,Human_RBP_ID_9392360,Human_RBP_ID_14485683,Human_RBP_ID_18789123,Human_RBP_ID_20784239,Human_RBP_ID_22270091,Human_RBP_ID_22820680,Human_RBP_ID_23013258,Human_RBP_ID_24494173,Human_RBP_ID_25670135,Human_RBP_ID_26345425,Human_RBP_ID_27037610,Human_RBP_ID_27308016,Human_RBP_ID_27494019 Human_Splice_Rec_2166895,Human_Splice_Rec_2166919,Human_Splice_Rec_2166921,Human_Splice_Rec_2166943 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_10529 90405 RMVar_ID_90405 Human_SNP_ID_703753271 m1A Human chr22 + 38489750 38489749 38489750 CCTAAAGTCCTGAATCACACCAGAAAGACGAGAAGGCACTTATCACAGGGGGCAGCTTGAGTCTC CCTAAAGTCCTGAATCACACCAGAAAGACGAG_AGGCACTTATCACAGGGGGCAGCTTGAGTCTC GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38489699..38489869 26863196 MeRIP-seq:(Medium) rs767112936 Functional Loss DEL dbSNP153 33..33 33 - - - 90406 RMVar_ID_90406 Human_SNP_ID_703753279 m1A Human chr22 - 38489795 38489795 38489795 CCCTGTAAATTCTTTTTTCCTTTGTTGCGTCAACGACCCTAGCCGGAGACTCAAGCTGCCCCCTG CCCTGTAAATTCTTTTTTCCTTTGTTGCGTCAGCGACCCTAGCCGGAGACTCAAGCTGCCCCCTG T C DDX17 Ensembl:ENSG00000100201 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38489699..38489900 26863196 MeRIP-seq:(Medium) rs186354659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65084,Human_RBP_ID_245826,Human_RBP_ID_580271,Human_RBP_ID_781193,Human_RBP_ID_833559,Human_RBP_ID_1942841,Human_RBP_ID_2718737,Human_RBP_ID_3672827,Human_RBP_ID_7081753,Human_RBP_ID_8550269,Human_RBP_ID_9126570,Human_RBP_ID_10057665,Human_RBP_ID_14485822,Human_RBP_ID_20762281,Human_RBP_ID_22270116,Human_RBP_ID_22820748,Human_RBP_ID_23013336,Human_RBP_ID_23947569,Human_RBP_ID_24494220,Human_RBP_ID_25682652,Human_RBP_ID_27037640,Human_RBP_ID_27708441 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_10529 90407 RMVar_ID_90407 Human_SNP_ID_703756868 m1A Human chr22 - 38501280 38501280 38501280 ACTGATGAACTAACTAAAAATTCTGTTCCTAGATTTGGAGCAAGAGGTGGTGGTGGCCTTCCCCC ACTGATGAACTAACTAAAAATTCTGTTCCTAGGTTTGGAGCAAGAGGTGGTGGTGGCCTTCCCCC T C DDX17 Ensembl:ENSG00000100201 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr22:38501251..38501300 26863196 MeRIP-seq:(Medium) rs781650280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_308022,Human_RBP_ID_833566,Human_RBP_ID_929458,Human_RBP_ID_1242310,Human_RBP_ID_3963278,Human_RBP_ID_14486458,Human_RBP_ID_19008073,Human_RBP_ID_22550765,Human_RBP_ID_22674321,Human_RBP_ID_22744352,Human_RBP_ID_23947691,Human_RBP_ID_24547146,Human_RBP_ID_25670577,Human_RBP_ID_27565370,Human_RBP_ID_27821317 Human_Splice_Rec_2166874,Human_Splice_Rec_2166898,Human_Splice_Rec_2166924,Human_Splice_Rec_2166952 RMVar_hsa_circ_90980,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_10529,RMVar_hsa_circ_293713,RMVar_hsa_circ_73592,RMVar_hsa_circ_214313,RMVar_hsa_circ_305533,RMVar_hsa_circ_214314,RMVar_hsa_circ_282548,RMVar_hsa_circ_7797,RMVar_hsa_circ_214317,RMVar_hsa_circ_214320,RMVar_hsa_circ_291422,RMVar_hsa_circ_214324,RMVar_hsa_circ_270924,RMVar_hsa_circ_125283,RMVar_hsa_circ_214323,RMVar_hsa_circ_367357,RMVar_hsa_circ_214326,RMVar_hsa_circ_214325,RMVar_hsa_circ_270804 90408 RMVar_ID_90408 Human_SNP_ID_703758508 m1A Human chr22 + 38506246 38506246 38506246 CGGGGCTACAAAGCCGGTGGGCAGGTTTGGCTACGCTCAAACCGGGCAGTGCCGCGGTTTAGGCG CGGGGCTACAAAGCCGGTGGGCAGGTTTGGCTGCGCTCAAACCGGGCAGTGCCGCGGTTTAGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:38505896..38506300;chr22:38506131..38506300;chr22:38505730..38506300;chr22:38505887..38506325 26863196 MeRIP-seq:(Medium) rs745762443 Functional Loss SNV dbSNP153 33..33 33 - - - 90409 RMVar_ID_90409 Human_SNP_ID_703758531 m1A Human chr22 - 38506279 38506277 38506279 GCCATTTTGTGCAGTCGCTGGGAAGGAAGGAGACGCCTAAACCGCGGCACTGCCCGGTTTGAGCG GCCATTTTGTGCAGTCGCTGGGAAGGAAGGAG__GCCTAAACCGCGGCACTGCCCGGTTTGAGCG CGT C DDX17 Ensembl:ENSG00000100201 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:38506198..38506304 26863410 MeRIP-seq:(Medium) rs1569145329 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_245844,Human_RBP_ID_781214,Human_RBP_ID_833577,Human_RBP_ID_931890,Human_RBP_ID_1611835,Human_RBP_ID_1942952,Human_RBP_ID_4708226,Human_RBP_ID_5149022,Human_RBP_ID_5324194,Human_RBP_ID_5530121,Human_RBP_ID_7082119,Human_RBP_ID_8865984,Human_RBP_ID_9300399,Human_RBP_ID_9332854,Human_RBP_ID_18423648,Human_RBP_ID_22086561,Human_RBP_ID_22454994,Human_RBP_ID_26762403,Human_RBP_ID_26770869 Human_miRNA_ID_2463529,Human_miRNA_ID_2516016,Human_miRNA_ID_2636170,Human_miRNA_ID_2638857,Human_miRNA_ID_2917572 RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214324,RMVar_hsa_circ_125283 90410 RMVar_ID_90410 Human_SNP_ID_703758538 m1A Human chr22 - 38506279 38506279 38506279 GCCATTTTGTGCAGTCGCTGGGAAGGAAGGAGACGCCTAAACCGCGGCACTGCCCGGTTTGAGCG GCCATTTTGTGCAGTCGCTGGGAAGGAAGGAGGCGCCTAAACCGCGGCACTGCCCGGTTTGAGCG T C DDX17 Ensembl:ENSG00000100201 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:38506198..38506304 26863410 MeRIP-seq:(Medium) rs778756322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245844,Human_RBP_ID_781214,Human_RBP_ID_833577,Human_RBP_ID_931890,Human_RBP_ID_1611835,Human_RBP_ID_1942952,Human_RBP_ID_4708226,Human_RBP_ID_5149022,Human_RBP_ID_5324194,Human_RBP_ID_5530121,Human_RBP_ID_7082119,Human_RBP_ID_8865984,Human_RBP_ID_9300399,Human_RBP_ID_9332854,Human_RBP_ID_18423648,Human_RBP_ID_22086561,Human_RBP_ID_22454994,Human_RBP_ID_26762403,Human_RBP_ID_26770869 Human_miRNA_ID_2463529,Human_miRNA_ID_2516016,Human_miRNA_ID_2636170,Human_miRNA_ID_2638857,Human_miRNA_ID_2917572 RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214324,RMVar_hsa_circ_125283 90411 RMVar_ID_90411 Human_SNP_ID_703789032 m1A Human chr22 - 38629929 38629929 38629929 GTAAAGGAGAGGCACCTGTGTGTGAGTGATGGATGGTAAAGAAGAGGCACGCTTCCTGATGGTAA GTAAAGGAGAGGCACCTGTGTGTGAGTGATGGCTGGTAAAGAAGAGGCACGCTTCCTGATGGTAA T G FAM227A Ensembl:ENSG00000184949 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38629889..38630202 26863196 MeRIP-seq:(Medium) rs564262966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23947825 RMVar_hsa_circ_5581,RMVar_hsa_circ_214341,RMVar_hsa_circ_374195,RMVar_hsa_circ_23867,RMVar_hsa_circ_47699,RMVar_hsa_circ_30641,RMVar_hsa_circ_214344 90412 RMVar_ID_90412 Human_SNP_ID_703789070 m1A Human chr22 + 38630047 38630047 38630047 TTTACCATCAGGAAGCGTGCCTCTTCTTTGCCATCACTCACACACAGGTGCCTCTCCTTTACCAT TTTACCATCAGGAAGCGTGCCTCTTCTTTGCCCTCACTCACACACAGGTGCCTCTCCTTTACCAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:38629993..38630093;chr22:38629883..38630238 26863196 MeRIP-seq:(Medium) rs1247475106 Functional Loss SNV dbSNP153 33..33 33 - - - 90413 RMVar_ID_90413 Human_SNP_ID_703789071 m1A Human chr22 + 38630047 38630047 38630047 TTTACCATCAGGAAGCGTGCCTCTTCTTTGCCATCACTCACACACAGGTGCCTCTCCTTTACCAT TTTACCATCAGGAAGCGTGCCTCTTCTTTGCCGTCACTCACACACAGGTGCCTCTCCTTTACCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:38629993..38630093;chr22:38629883..38630238 26863196 MeRIP-seq:(Medium) rs1247475106 Functional Loss SNV dbSNP153 33..33 33 - - - 90414 RMVar_ID_90414 Human_SNP_ID_703796808 m1A Human chr22 + 38656718 38656718 38656718 TGGGCTACAGAGTCCTTGCTGGGGGTTCGGGGAGCGCTTGGACCCCGGCTTCTGGGACGCGTCAG TGGGCTACAGAGTCCTTGCTGGGGGTTCGGGGGGCGCTTGGACCCCGGCTTCTGGGACGCGTCAG A G CBY1 Ensembl:ENSG00000100211 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38656668..38656991 26863196 MeRIP-seq:(Medium) rs539698122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246547,Human_RBP_ID_4708643,Human_RBP_ID_18423649,Human_RBP_ID_23947842 Human_Splice_Rec_2167259,Human_Splice_Rec_2167261,Human_Splice_Rec_2167265,Human_Splice_Rec_2167273,Human_Splice_Rec_2167283,Human_Splice_Rec_2167291,Human_Splice_Rec_2167297,Human_Splice_Rec_2167303,Human_Splice_Rec_2167313 90415 RMVar_ID_90415 Human_SNP_ID_703803346 m1A Human chr22 + 38682019 38682019 38682019 CGCCGTCGCTGCTGCCGGTGCAGGGGAACCCCAGTCCCCGGACGAATTGCTCCCGAAAGGCGACG CGCCGTCGCTGCTGCCGGTGCAGGGGAACCCCCGTCCCCGGACGAATTGCTCCCGAAAGGCGACG A C TOMM22 Ensembl:ENSG00000100216 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38681951..38682075 26863196 MeRIP-seq:(Medium) rs1040272071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65969,Human_RBP_ID_580385,Human_RBP_ID_782215,Human_RBP_ID_1611861,Human_RBP_ID_4708227,Human_RBP_ID_9333379,Human_RBP_ID_22454674,Human_RBP_ID_26345995 Human_Splice_Rec_2167349 90416 RMVar_ID_90416 Human_SNP_ID_703803347 m1A Human chr22 + 38682019 38682019 38682019 CGCCGTCGCTGCTGCCGGTGCAGGGGAACCCCAGTCCCCGGACGAATTGCTCCCGAAAGGCGACG CGCCGTCGCTGCTGCCGGTGCAGGGGAACCCCGGTCCCCGGACGAATTGCTCCCGAAAGGCGACG A G TOMM22 Ensembl:ENSG00000100216 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38681951..38682075 26863196 MeRIP-seq:(Medium) rs1040272071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65969,Human_RBP_ID_580385,Human_RBP_ID_782215,Human_RBP_ID_1611861,Human_RBP_ID_4708227,Human_RBP_ID_9333379,Human_RBP_ID_22454674,Human_RBP_ID_26345995 Human_Splice_Rec_2167349 90417 RMVar_ID_90417 Human_SNP_ID_703803453 m1A Human chr22 - 38682284 38682284 38682284 TGGAGTAGACGCGGGTCTTAGCCGAAAAAGCGACATCCATTCCTGGCCCCGCTGCGGCACTGGGA TGGAGTAGACGCGGGTCTTAGCCGAAAAAGCGTCATCCATTCCTGGCCCCGCTGCGGCACTGGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38682282..38682388 26863196 MeRIP-seq:(Medium) rs745885334 Functional Loss SNV dbSNP153 33..33 33 - - - 90418 RMVar_ID_90418 Human_SNP_ID_703803454 m1A Human chr22 - 38682284 38682284 38682284 TGGAGTAGACGCGGGTCTTAGCCGAAAAAGCGACATCCATTCCTGGCCCCGCTGCGGCACTGGGA TGGAGTAGACGCGGGTCTTAGCCGAAAAAGCGCCATCCATTCCTGGCCCCGCTGCGGCACTGGGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38682282..38682388 26863196 MeRIP-seq:(Medium) rs745885334 Functional Loss SNV dbSNP153 33..33 33 - - - 90419 RMVar_ID_90419 Human_SNP_ID_703803499 m1A Human chr22 + 38682401 38682401 38682401 TTCCGGAGAGGGTCCGGTCCGCGGCCGGAGCCACTTTTGATCTTTCCCTCTTTGTGGCTCAGAAA TTCCGGAGAGGGTCCGGTCCGCGGCCGGAGCCTCTTTTGATCTTTCCCTCTTTGTGGCTCAGAAA A T TOMM22 Ensembl:ENSG00000100216 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38682351..38682450 32194978 MeRIP-seq:(Medium) rs1403069746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4709059,Human_RBP_ID_14487509,Human_RBP_ID_17989435,Human_RBP_ID_22454997,Human_RBP_ID_23212944,Human_RBP_ID_26345435,Human_RBP_ID_27037812 Human_Splice_Rec_2167350,Human_Splice_Rec_2167351,Human_Splice_Rec_2167355 90420 RMVar_ID_90420 Human_SNP_ID_703804123 m1A Human chr22 + 38684367 38684367 38684367 CTGCAGCTTCAGCCACAGAATGGGGACTATGGAAGACAGCAGGAGCTCATTTCCTCTGCACATTT CTGCAGCTTCAGCCACAGAATGGGGACTATGGCAGACAGCAGGAGCTCATTTCCTCTGCACATTT A C TOMM22 Ensembl:ENSG00000100216 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs553396357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580424,Human_RBP_ID_1029379,Human_RBP_ID_1611875,Human_RBP_ID_1942969,Human_RBP_ID_2718872,Human_RBP_ID_3672952,Human_RBP_ID_7082292,Human_RBP_ID_9126664,Human_RBP_ID_14487578,Human_RBP_ID_17286035,Human_RBP_ID_17399222,Human_RBP_ID_17989544,Human_RBP_ID_18329337,Human_RBP_ID_18789339,Human_RBP_ID_23947909 90421 RMVar_ID_90421 Human_SNP_ID_703808407 m1A Human chr22 - 38700479 38700479 38700479 CGCGGTCCCACGCCTGCCGGCCCGCGCTAGCTACTCGACTCGTGCGCTAAATTTATCCGTCACCC CGCGGTCCCACGCCTGCCGGCCCGCGCTAGCTGCTCGACTCGTGCGCTAAATTTATCCGTCACCC T C JOSD1 Ensembl:ENSG00000100221 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38700401..38700700 26863196 MeRIP-seq:(Medium) rs962792752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580497,Human_RBP_ID_4697841 90422 RMVar_ID_90422 Human_SNP_ID_703808408 m1A Human chr22 - 38700479 38700479 38700479 CGCGGTCCCACGCCTGCCGGCCCGCGCTAGCTACTCGACTCGTGCGCTAAATTTATCCGTCACCC CGCGGTCCCACGCCTGCCGGCCCGCGCTAGCTCCTCGACTCGTGCGCTAAATTTATCCGTCACCC T G JOSD1 Ensembl:ENSG00000100221 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:38700401..38700700 26863196 MeRIP-seq:(Medium) rs962792752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580497,Human_RBP_ID_4697841 90423 RMVar_ID_90423 Human_SNP_ID_703808534 m1A Human chr22 - 38700837 38700837 38700837 GCCCTGGGGTCTGCGGCCGGGGGCGCGGCGGGAGGGCGTCTGGGCCTGCGCTCACGTGACGGGCG GCCCTGGGGTCTGCGGCCGGGGGCGCGGCGGGGGGGCGTCTGGGCCTGCGCTCACGTGACGGGCG T C JOSD1 Ensembl:ENSG00000100221 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:38700716..38700908 26863196 MeRIP-seq:(Medium) rs1010691289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4697859,Human_RBP_ID_9332855,Human_RBP_ID_22550768,Human_RBP_ID_22725145 Human_Splice_Rec_2167389 90424 RMVar_ID_90424 Human_SNP_ID_703808535 m1A Human chr22 - 38700837 38700837 38700837 GCCCTGGGGTCTGCGGCCGGGGGCGCGGCGGGAGGGCGTCTGGGCCTGCGCTCACGTGACGGGCG GCCCTGGGGTCTGCGGCCGGGGGCGCGGCGGGCGGGCGTCTGGGCCTGCGCTCACGTGACGGGCG T G JOSD1 Ensembl:ENSG00000100221 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:38700716..38700908 26863196 MeRIP-seq:(Medium) rs1010691289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4697859,Human_RBP_ID_9332855,Human_RBP_ID_22550768,Human_RBP_ID_22725145 Human_Splice_Rec_2167389 90425 RMVar_ID_90425 Human_SNP_ID_703810417 m1A Human chr22 - 38706004 38706004 38706004 CCCCGGGGAGCTGGGCTCGGGGGCGAACATAGAGGCCGGGACCGGCGAGTCCATCGCGGAGCGAC CCCCGGGGAGCTGGGCTCGGGGGCGAACATAGGGGCCGGGACCGGCGAGTCCATCGCGGAGCGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38705951..38706534 26863196 MeRIP-seq:(Medium) rs1365706173 Functional Loss SNV dbSNP153 33..33 33 - - - 90426 RMVar_ID_90426 Human_SNP_ID_703810434 m1A Human chr22 + 38706043 38706043 38706043 TCGCCCCCGAGCCCAGCTCCCCGGGGGCGGCCAGGGCCGCGGCGGCCGCCGCCCGACTCCACGGC TCGCCCCCGAGCCCAGCTCCCCGGGGGCGGCCGGGGCCGCGGCGGCCGCCGCCCGACTCCACGGC A G GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr22:38705951..38706150;chr22:38705951..38706120 26863196,26863410 MeRIP-seq:(Medium) rs955471735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782221,Human_RBP_ID_4709066,Human_RBP_ID_8865986,Human_RBP_ID_9300401,Human_RBP_ID_22454468 90427 RMVar_ID_90427 Human_SNP_ID_703811116 m1A Human chr22 - 38708743 38708743 38708743 TAGCCTAACCAAAGATCCTGACTGAACCCCATAGCACCCTCATCTAAAAAGGCTGCACAGCCCCT TAGCCTAACCAAAGATCCTGACTGAACCCCATTGCACCCTCATCTAAAAAGGCTGCACAGCCCCT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:38708733..38708950 26863196 MeRIP-seq:(Medium) rs1450707174 Functional Loss SNV dbSNP153 33..33 33 - - - 90428 RMVar_ID_90428 Human_SNP_ID_703811120 m1A Human chr22 - 38708750 38708750 38708750 ATCAATATAGCCTAACCAAAGATCCTGACTGAACCCCATAGCACCCTCATCTAAAAAGGCTGCAC ATCAATATAGCCTAACCAAAGATCCTGACTGAGCCCCATAGCACCCTCATCTAAAAAGGCTGCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:38708745..38708875 26863196 MeRIP-seq:(Medium) rs1233025178 Functional Loss SNV dbSNP153 33..33 33 - - - 90429 RMVar_ID_90429 Human_SNP_ID_703812170 m1A Human chr22 + 38713511 38713511 38713511 CTGCGGATTGGCAAAAAGGGCAGACATCAGGGAAGGAGGCAAGGTAAAATGCTAGAATCATCAGG CTGCGGATTGGCAAAAAGGGCAGACATCAGGGCAGGAGGCAAGGTAAAATGCTAGAATCATCAGG A C GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38713507..38713586 26863196 MeRIP-seq:(Medium) rs1474727216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357 90430 RMVar_ID_90430 Human_SNP_ID_703812171 m1A Human chr22 + 38713511 38713511 38713511 CTGCGGATTGGCAAAAAGGGCAGACATCAGGGAAGGAGGCAAGGTAAAATGCTAGAATCATCAGG CTGCGGATTGGCAAAAAGGGCAGACATCAGGGGAGGAGGCAAGGTAAAATGCTAGAATCATCAGG A G GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38713507..38713586 26863196 MeRIP-seq:(Medium) rs1474727216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357 90431 RMVar_ID_90431 Human_SNP_ID_703812788 m1A Human chr22 - 38716000 38715998 38716001 CGCGGCCCCCAGCTTCTTGCCGTTCCCGCAGAAGGATGACATCGGCCTCTATCTGTTCCGCCATG CGCGGCCCCCAGCTTCTTGCCGTTCCCGCAG___GATGACATCGGCCTCTATCTGTTCCGCCATG CCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38715951..38716117 26863196 MeRIP-seq:(Medium) rs1420624522 Functional Loss DEL dbSNP153 32..34 33 - - - 90432 RMVar_ID_90432 Human_SNP_ID_703812974 m1A Human chr22 + 38716615 38716615 38716615 TTATGATGGTCGCTCCACCTCACTCATTCACTAACTCTCACATAGATGTATGGGTTCATCTACAC TTATGATGGTCGCTCCACCTCACTCATTCACTGACTCTCACATAGATGTATGGGTTCATCTACAC A G GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38716612..38716852 26863196 MeRIP-seq:(Medium) rs369844031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83544,RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_105332,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357,RMVar_hsa_circ_265149,RMVar_hsa_circ_271972,RMVar_hsa_circ_114152,RMVar_hsa_circ_214360,RMVar_hsa_circ_214361,RMVar_hsa_circ_214362,RMVar_hsa_circ_214359 90433 RMVar_ID_90433 Human_SNP_ID_703812975 m1A Human chr22 + 38716615 38716615 38716615 TTATGATGGTCGCTCCACCTCACTCATTCACTAACTCTCACATAGATGTATGGGTTCATCTACAC TTATGATGGTCGCTCCACCTCACTCATTCACTTACTCTCACATAGATGTATGGGTTCATCTACAC A T GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38716612..38716852 26863196 MeRIP-seq:(Medium) rs369844031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83544,RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_105332,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357,RMVar_hsa_circ_265149,RMVar_hsa_circ_271972,RMVar_hsa_circ_114152,RMVar_hsa_circ_214360,RMVar_hsa_circ_214361,RMVar_hsa_circ_214362,RMVar_hsa_circ_214359 90434 RMVar_ID_90434 Human_SNP_ID_703812990 m1A Human chr22 + 38716655 38716655 38716655 CATAGATGTATGGGTTCATCTACACGCAGGGTAGCAGTGGTGGGCAACGTGGATGCTGGCAAAAG CATAGATGTATGGGTTCATCTACACGCAGGGTGGCAGTGGTGGGCAACGTGGATGCTGGCAAAAG A G GTPBP1 Ensembl:ENSG00000100226 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38716651..38716700 32194978 MeRIP-seq:(Medium) rs375245204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_932338,Human_RBP_ID_8865751,Human_RBP_ID_19008076,Human_RBP_ID_22454470 Human_Splice_Rec_2167396,Human_Splice_Rec_2167402,Human_Splice_Rec_2167422,Human_Splice_Rec_2167434 RMVar_hsa_circ_83544,RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_105332,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357,RMVar_hsa_circ_265149,RMVar_hsa_circ_271972,RMVar_hsa_circ_114152,RMVar_hsa_circ_214360,RMVar_hsa_circ_214361,RMVar_hsa_circ_214362,RMVar_hsa_circ_214359,RMVar_hsa_circ_114636,RMVar_hsa_circ_124820,RMVar_hsa_circ_371080,RMVar_hsa_circ_214363,RMVar_hsa_circ_214364,RMVar_hsa_circ_214365 90435 RMVar_ID_90435 Human_SNP_ID_703813026 m1A Human chr22 - 38716826 38716826 38716826 TGGCTGTCAGGCTTGTTCACTACATTGCCTTCACTGTCAAAGCCCAGAATGTCGTTGCCCACACT TGGCTGTCAGGCTTGTTCACTACATTGCCTTCTCTGTCAAAGCCCAGAATGTCGTTGCCCACACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38716775..38716907 26863196 MeRIP-seq:(Medium) rs745400646 Functional Loss SNV dbSNP153 33..33 33 - - - 90436 RMVar_ID_90436 Human_SNP_ID_703817526 m1A Human chr22 + 38734974 38734974 38734974 CCTTCTTGCCCCTTCCCCGCAGCCAGACCACCAGACACAGCCGGAACCAGTGCCCCAGGCCCCTC CCTTCTTGCCCCTTCCCCGCAGCCAGACCACCGGACACAGCCGGAACCAGTGCCCCAGGCCCCTC A G AL021707.5,GTPBP1,AL021707.3 Ensembl:ENSG00000244491,Ensembl:ENSG00000100226,Ensembl:ENSG00000230149 lincRNA,Protein coding,lincRNA exon,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38734924..38735024 32194978 MeRIP-seq:(Medium) rs1269093852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8262948 Human_Splice_Rec_2167473 90437 RMVar_ID_90437 Human_SNP_ID_703818578 m1A Human chr22 - 38738670 38738670 38738670 CCGTGGTCCGCCTCTCTGCCCGCATCCGCCCCACAGCCGTTACCTTAGAGCATGTGCCCAAGGCC CCGTGGTCCGCCTCTCTGCCCGCATCCGCCCCCCAGCCGTTACCTTAGAGCATGTGCCCAAGGCC T G SUN2 Ensembl:ENSG00000100242 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38738620..38738939 32194978 MeRIP-seq:(Medium) rs117425989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18471487,Human_RBP_ID_21896802,Human_RBP_ID_22454474 Human_Splice_Rec_2167506,Human_Splice_Rec_2167507,Human_Splice_Rec_2167540,Human_Splice_Rec_2167541,Human_Splice_Rec_2167576,Human_Splice_Rec_2167577,Human_Splice_Rec_2167584,Human_Splice_Rec_2167585,Human_Splice_Rec_2167588,Human_Splice_Rec_2167589 Human_miRNA_ID_2387603,Human_miRNA_ID_2389075,Human_miRNA_ID_2400224,Human_miRNA_ID_3031291 RMVar_hsa_circ_13876,RMVar_hsa_circ_46550,RMVar_hsa_circ_51048,RMVar_hsa_circ_41477,RMVar_hsa_circ_128210,RMVar_hsa_circ_268178,RMVar_hsa_circ_214372 90438 RMVar_ID_90438 Human_SNP_ID_703819828 m1A Human chr22 + 38742687 38742687 38742687 GATTCCAGAGACGTTCCAGCATAAGGCCATGCAGGGCCGGCTGGAGCTCGTGGGCAGGGGCTGCC GATTCCAGAGACGTTCCAGCATAAGGCCATGCGGGGCCGGCTGGAGCTCGTGGGCAGGGGCTGCC A G AL021707.6,AL021707.1 Ensembl:ENSG00000272669,Ensembl:ENSG00000225450 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:38742669..38742810;chr22:38742685..38742783 26863196 MeRIP-seq:(Medium) rs541968957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5601050 90439 RMVar_ID_90439 Human_SNP_ID_703825028 m1A Human chr22 - 38761672 38761672 38761672 CGCACACACATTCACACACACTCCCCACACACACTCACACTCATACACACACACATTCACACACT CGCACACACATTCACACACACTCCCCACACACTCTCACACTCATACACACACACATTCACACACT T A SUN2 Ensembl:ENSG00000100242 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38761621..38761964 26863196 MeRIP-seq:(Medium) rs573069287 Functional Loss SNV dbSNP153 33..33 33 - - - 90440 RMVar_ID_90440 Human_SNP_ID_703825036 m1A Human chr22 - 38761695 38761683 38761695 ACACACATACATATTCACACACTCGCACACACATTCACACACACTCCCCACACACACTCACACTC ACACACATACATATTCACACACTCGCACACAC____________TCCCCACACACACTCACACTC AGTGTGTGTGAAT A SUN2 Ensembl:ENSG00000100242 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38761599..38761788 26863196 MeRIP-seq:(Medium) rs1455699632 Functional Loss DEL dbSNP153 33..44 33 - - - 90441 RMVar_ID_90441 Human_SNP_ID_703825042 m1A Human chr22 - 38761695 38761694 38761696 ACACACATACATATTCACACACTCGCACACACATTCACACACACTCCCCACACACACTCACACTC ACACACATACATATTCACACACTCGCACACA__TTCACACACACTCCCCACACACACTCACACTC ATG A SUN2 Ensembl:ENSG00000100242 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38761599..38761788 26863196 MeRIP-seq:(Medium) rs955996731 Functional Loss DEL dbSNP153 32..33 33 - - - 90442 RMVar_ID_90442 Human_SNP_ID_703825329 m1A Human chr22 + 38761980 38761980 38761980 ATGTGTGAGTGTGCGTGTGTGAATGTGTGAGAATTATGTGTGTGAATGTGTGTGCATGTTTGTGT ATGTGTGAGTGTGCGTGTGTGAATGTGTGAGATTTATGTGTGTGAATGTGTGTGCATGTTTGTGT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38761936..38762021 26863196 MeRIP-seq:(Medium) rs865873697 Functional Loss SNV dbSNP153 33..33 33 - - - 90443 RMVar_ID_90443 Human_SNP_ID_703829980 m1A Human chr22 + 38779201 38779198 38779201 ACCTCCTCTACCCTGTCACACCGCCCCACCCCACGTCTCCCACACAGACCCATGCCCGCTGCCCC ACCTCCTCTACCCTGTCACACCGCCCCACC___CGTCTCCCACACAGACCCATGCCCGCTGCCCC CCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38779151..38779244 26863196 MeRIP-seq:(Medium) rs1217118152 Functional Loss DEL dbSNP153 31..33 33 - - - 90444 RMVar_ID_90444 Human_SNP_ID_703831044 m1A Human chr22 + 38783261 38783261 38783261 TACACACACGGGCCTTCCCTCCCACTACACACACGGGCCTTCCCTCCCACTACATACACGGGCCT TACACACACGGGCCTTCCCTCCCACTACACACGCGGGCCTTCCCTCCCACTACATACACGGGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38783258..38783345 26863196 MeRIP-seq:(Medium) rs1369694122 Functional Loss SNV dbSNP153 33..33 33 - - - 90445 RMVar_ID_90445 Human_SNP_ID_703833792 m1A Human chr22 + 38794108 38794108 38794108 GCGGGGGCCGGAGCCGGGGCCGCAGCCAGCGAACCCCCGCCAGGGTTGTCAAGGAGCGAAACAAG GCGGGGGCCGGAGCCGGGGCCGCAGCCAGCGACCCCCCGCCAGGGTTGTCAAGGAGCGAAACAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38794035..38794116 26863196 MeRIP-seq:(Medium) rs550921052 Functional Loss SNV dbSNP153 33..33 33 - - - 90446 RMVar_ID_90446 Human_SNP_ID_703833805 m1A Human chr22 + 38794127 38794127 38794127 CCGCAGCCAGCGAACCCCCGCCAGGGTTGTCAAGGAGCGAAACAAGAGTGTCTTAGCAACCAGCA CCGCAGCCAGCGAACCCCCGCCAGGGTTGTCAGGGAGCGAAACAAGAGTGTCTTAGCAACCAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38794050..38794147 26863196 MeRIP-seq:(Medium) rs894481356 Functional Loss SNV dbSNP153 33..33 33 - - - 90447 RMVar_ID_90447 Human_SNP_ID_703842964 m1A Human chr22 + 38828218 38828218 38828218 AGTCTGTCGATGTTAGCCTCCGGGGAGCATGGATATATTTTTTGAATGGCTCTGTCATCCTGAGG AGTCTGTCGATGTTAGCCTCCGGGGAGCATGGGTATATTTTTTGAATGGCTCTGTCATCCTGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38828201..38828288 26863196 MeRIP-seq:(Medium) rs1478300088 Functional Loss SNV dbSNP153 33..33 33 - - - 90448 RMVar_ID_90448 Human_SNP_ID_703851337 m1A Human chr22 + 38862190 38862190 38862190 TGGAGTGAGGCACTGACTCCTCCAAAGATTGCAGGGGGCGGAGGAGGGAACCACGAAGGCCTGGG TGGAGTGAGGCACTGACTCCTCCAAAGATTGCTGGGGGCGGAGGAGGGAACCACGAAGGCCTGGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38862147..38862298 32194978 MeRIP-seq:(Medium) rs971244553 Functional Loss SNV dbSNP153 33..33 33 - - - 90449 RMVar_ID_90449 Human_SNP_ID_703851689 m1A Human chr22 - 38863207 38863207 38863207 GTAAGTTGGGACCCATCCCTGTCTGGGTGCCCACTCTGACCTTTAGTTTGCCCTTCTGTGAAATG GTAAGTTGGGACCCATCCCTGTCTGGGTGCCCCCTCTGACCTTTAGTTTGCCCTTCTGTGAAATG T G CBX6 Ensembl:ENSG00000183741 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38863157..38863241 26863196 MeRIP-seq:(Medium) rs1347102636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580629,Human_RBP_ID_1201793,Human_RBP_ID_7082623,Human_RBP_ID_8207944,Human_RBP_ID_14488983,Human_RBP_ID_18329387,Human_RBP_ID_18789455,Human_RBP_ID_26498554,Human_RBP_ID_27841292 90450 RMVar_ID_90450 Human_SNP_ID_703852719 m1A Human chr22 - 38866522 38866522 38866522 GACCGTGAGCCCATCCGCCCCCAGCTGGCGCGAGCCGGAGGTGCTCGACCTGTCCCTCCCTCCCG GACCGTGAGCCCATCCGCCCCCAGCTGGCGCGTGCCGGAGGTGCTCGACCTGTCCCTCCCTCCCG T A CBX6 Ensembl:ENSG00000183741 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr22:38866473..38866666;chr22:38866476..38866675 26863196 MeRIP-seq:(Medium) rs1422111861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27494189 Human_miRNA_ID_208773,Human_miRNA_ID_2017432 RMVar_hsa_circ_106462,RMVar_hsa_circ_123149,RMVar_hsa_circ_116042,RMVar_hsa_circ_214377,RMVar_hsa_circ_214378,RMVar_hsa_circ_214379 90451 RMVar_ID_90451 Human_SNP_ID_703853063 m1A Human chr22 - 38867185 38867185 38867185 CTCCCTCTGCCCGCAGGCGCGGGCCCAGGCCGAGGCCCTCCGCATCAGTGATGTGCATTTCTCTG CTCCCTCTGCCCGCAGGCGCGGGCCCAGGCCGGGGCCCTCCGCATCAGTGATGTGCATTTCTCTG T C CBX6 Ensembl:ENSG00000183741 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:38866386..38869605 32194978 MeRIP-seq:(Medium) rs982574884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_931019,Human_RBP_ID_19112132 Human_Splice_Rec_2167734 RMVar_hsa_circ_106462,RMVar_hsa_circ_123149,RMVar_hsa_circ_116042,RMVar_hsa_circ_214377,RMVar_hsa_circ_214378,RMVar_hsa_circ_214379 90452 RMVar_ID_90452 Human_SNP_ID_703883573 m1A Human chr22 - 38986377 38986377 38986377 AGAATCTCCTTTAGCGTGCGGTGCAGGAATGCATAATTTTCATCGAATTTGTACCAAGGCATGAA AGAATCTCCTTTAGCGTGCGGTGCAGGAATGCGTAATTTTCATCGAATTTGTACCAAGGCATGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38986326..38986400 32194978 MeRIP-seq:(Medium) rs770347240 Functional Loss SNV dbSNP153 33..33 33 - - - 90453 RMVar_ID_90453 Human_SNP_ID_703891650 m1A Human chr22 + 39014286 39014286 39014286 GTCACTTTAAAGAGGGCTGCTCAACTGCAAGGACGCTGTAAGCAGGAAGAGAAGCCACAGCGCTT GTCACTTTAAAGAGGGCTGCTCAACTGCAAGGGCGCTGTAAGCAGGAAGAGAAGCCACAGCGCTT A G APOBEC3C Ensembl:ENSG00000244509 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:39014179..39015595;chr22:39014213..39014400 26863196 MeRIP-seq:(Medium) rs1286731643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708653,Human_RBP_ID_5119934,Human_RBP_ID_22455251 Human_Splice_Rec_2167843,Human_Splice_Rec_2167849,Human_Splice_Rec_2167853 90454 RMVar_ID_90454 Human_SNP_ID_703891671 m1A Human chr22 - 39014329 39014329 39014329 TTCAGCCTCTTAGATATGCTTGTCCCTGTCCCACTCTTTTCTGAAGCGCTGTGGCTTCTCTTCCT TTCAGCCTCTTAGATATGCTTGTCCCTGTCCCGCTCTTTTCTGAAGCGCTGTGGCTTCTCTTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39014280..39014354 26863196 MeRIP-seq:(Medium) rs959919042 Functional Loss SNV dbSNP153 33..33 33 - - - 90455 RMVar_ID_90455 Human_SNP_ID_703891672 m1A Human chr22 - 39014329 39014329 39014329 TTCAGCCTCTTAGATATGCTTGTCCCTGTCCCACTCTTTTCTGAAGCGCTGTGGCTTCTCTTCCT TTCAGCCTCTTAGATATGCTTGTCCCTGTCCCCCTCTTTTCTGAAGCGCTGTGGCTTCTCTTCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39014280..39014354 26863196 MeRIP-seq:(Medium) rs959919042 Functional Loss SNV dbSNP153 33..33 33 - - - 90456 RMVar_ID_90456 Human_SNP_ID_703893221 m1A Human chr22 - 39018531 39018530 39018531 AGTCTGGAAGAGCGAGGAGGAAGCGGTGAGGCAGGGGAGCACTGTGGAATGGCCCTGAGGCCAGG AGTCTGGAAGAGCGAGGAGGAAGCGGTGAGGC_GGGGAGCACTGTGGAATGGCCCTGAGGCCAGG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39018424..39018721 26863196 MeRIP-seq:(Medium) rs1421377505 Functional Loss DEL dbSNP153 33..33 33 - - - 90457 RMVar_ID_90457 Human_SNP_ID_703893263 m1A Human chr22 + 39018644 39018644 39018644 ACAGACCCCGTTCCTCCAGCCTGCGTGCCCCTAACCTGGCTTTTCCCATCTCCCCAGCATAACCA ACAGACCCCGTTCCTCCAGCCTGCGTGCCCCTTACCTGGCTTTTCCCATCTCCCCAGCATAACCA A T APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:39018532..39018701 26863196 MeRIP-seq:(Medium) rs945793329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119935,Human_RBP_ID_17286970,Human_RBP_ID_17400035,Human_RBP_ID_18952628,Human_RBP_ID_21938099 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 90458 RMVar_ID_90458 Human_SNP_ID_703893658 m1A Human chr22 + 39020030 39020030 39020030 GTTGGCCAGACTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCTGTCTCAGCCTCTCCAAGTGC GTTGGCCAGACTGGTCTCGAACTCCTGACCTCGGGTGATCCGCCTGTCTCAGCCTCTCCAAGTGC A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1282635675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5653474,Human_RBP_ID_26501079 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 90459 RMVar_ID_90459 Human_SNP_ID_703893666 m1A Human chr22 + 39020076 39020076 39020076 TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCATCAGCCACTATGCCCGGCTGGGATCATATGTT TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCGTCAGCCACTATGCCCGGCTGGGATCATATGTT A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112668427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5653474,Human_RBP_ID_17573079,Human_RBP_ID_26500296 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 90460 RMVar_ID_90460 Human_SNP_ID_703893667 m1A Human chr22 + 39020076 39020076 39020076 TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCATCAGCCACTATGCCCGGCTGGGATCATATGTT TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCTTCAGCCACTATGCCCGGCTGGGATCATATGTT A T APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112668427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5653474,Human_RBP_ID_17573079,Human_RBP_ID_26500296 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 90461 RMVar_ID_90461 Human_SNP_ID_703893673 m1A Human chr22 - 39020095 39020095 39020095 ATTGAACAAACATGTGTGGAACATATGATCCCAGCCGGGCATAGTGGCTGATGCCTGTAATCCCA ATTGAACAAACATGTGTGGAACATATGATCCCCGCCGGGCATAGTGGCTGATGCCTGTAATCCCA T G HSALNG0135466 RNACentral:URS0000EB9607 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39020047..39020200 26863196 MeRIP-seq:(Medium) rs1360788038 Functional Loss SNV dbSNP153 33..33 33 - - - 90462 RMVar_ID_90462 Human_SNP_ID_703928251 m1A Human chr22 + 39138714 39138714 39138714 GATGCTCGGTCTCTCTCCTCCCTGGGGTGTGAAGCAGGTGGCAGAAGAAAAGGAAACACTGGTGA GATGCTCGGTCTCTCTCCTCCCTGGGGTGTGAGGCAGGTGGCAGAAGAAAAGGAAACACTGGTGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39138708..39138870 32194978 MeRIP-seq:(Medium) rs1266236377 Functional Loss SNV dbSNP153 33..33 33 - - - 90463 RMVar_ID_90463 Human_SNP_ID_703956317 m1A Human chr22 - 39243184 39243183 39243184 TAGAGACGCAGGTAGGTTTCGGGCACTCGGGTAGGGGGAGGACTAGGGGCTCTGAAGGAATCCAG TAGAGACGCAGGTAGGTTTCGGGCACTCGGGT_GGGGGAGGACTAGGGGCTCTGAAGGAATCCAG CT C PDGFB Ensembl:ENSG00000100311 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39243177..39243245 26863196 MeRIP-seq:(Medium) rs962036295 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18463977 90464 RMVar_ID_90464 Human_SNP_ID_703956975 m1A Human chr22 + 39244915 39244904 39244916 CGCTGGCGGCCGGAGGGGAGCCCTAGGGAGGCAGCGGGGGAGGCTGCGGGTGCGCAGGGAGGCAG CGCTGGCGGCCGGAGGGGAGCC____________CGGGGGAGGCTGCGGGTGCGCAGGGAGGCAG CCTAGGGAGGCAG C AL031590.1 Ensembl:ENSG00000284633 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:39244871..39244954 26863196 MeRIP-seq:(Medium) rs1236787683 Functional Loss DEL dbSNP153 23..34 33 - - - 90465 RMVar_ID_90465 Human_SNP_ID_703956980 m1A Human chr22 + 39244915 39244915 39244915 CGCTGGCGGCCGGAGGGGAGCCCTAGGGAGGCAGCGGGGGAGGCTGCGGGTGCGCAGGGAGGCAG CGCTGGCGGCCGGAGGGGAGCCCTAGGGAGGCGGCGGGGGAGGCTGCGGGTGCGCAGGGAGGCAG A G AL031590.1 Ensembl:ENSG00000284633 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:39244871..39244954 26863196 MeRIP-seq:(Medium) rs1254913071 Functional Loss SNV dbSNP153 33..33 33 - - - 90466 RMVar_ID_90466 Human_SNP_ID_703975821 m1A Human chr22 - 39313900 39313900 39313900 AGAAGTGGGGTCTCAGGCTCAGCTGTTCAGTGATGAGGCCTGGAATGTGCGCTGGGCACAGCGCC AGAAGTGGGGTCTCAGGCTCAGCTGTTCAGTGTTGAGGCCTGGAATGTGCGCTGGGCACAGCGCC T A SNORD83B,RPL3 Ensembl:ENSG00000209480,Ensembl:ENSG00000100316 snoRNA,Protein coding exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39313629..39313929 32194978 MeRIP-seq:(Medium) rs770266351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64784,Human_RBP_ID_780833,Human_RBP_ID_833084,Human_RBP_ID_931329,Human_RBP_ID_1136864,Human_RBP_ID_1382713,Human_RBP_ID_1612041,Human_RBP_ID_1943040,Human_RBP_ID_2718998,Human_RBP_ID_3673043,Human_RBP_ID_5101851,Human_RBP_ID_5298807,Human_RBP_ID_5601716,Human_RBP_ID_7082851,Human_RBP_ID_8262362,Human_RBP_ID_8550553,Human_RBP_ID_8866271,Human_RBP_ID_9128508,Human_RBP_ID_9260802,Human_RBP_ID_9299954,Human_RBP_ID_9341365,Human_RBP_ID_9434508,Human_RBP_ID_14489464,Human_RBP_ID_17088483,Human_RBP_ID_17149042,Human_RBP_ID_17287432,Human_RBP_ID_17515270,Human_RBP_ID_17573348,Human_RBP_ID_17583821,Human_RBP_ID_17671192,Human_RBP_ID_17702370,Human_RBP_ID_17986500,Human_RBP_ID_18201462,Human_RBP_ID_18445499,Human_RBP_ID_18544761,Human_RBP_ID_18789493,Human_RBP_ID_20782783,Human_RBP_ID_22007485,Human_RBP_ID_22371887,Human_RBP_ID_22425761,Human_RBP_ID_22508384,Human_RBP_ID_22526265,Human_RBP_ID_22531690,Human_RBP_ID_22551265,Human_RBP_ID_22675897,Human_RBP_ID_22705945,Human_RBP_ID_22725550,Human_RBP_ID_22744362,Human_RBP_ID_22768493,Human_RBP_ID_23111765,Human_RBP_ID_23115780,Human_RBP_ID_23119905,Human_RBP_ID_23134434,Human_RBP_ID_23286160,Human_RBP_ID_23948226,Human_RBP_ID_24547154,Human_RBP_ID_24553887,Human_RBP_ID_24561191,Human_RBP_ID_26501321,Human_RBP_ID_26750410,Human_RBP_ID_26790067,Human_RBP_ID_27159483,Human_RBP_ID_27708526 RMVar_hsa_circ_92264,RMVar_hsa_circ_101826,RMVar_hsa_circ_214388,RMVar_hsa_circ_110607,RMVar_hsa_circ_214385,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_76609,RMVar_hsa_circ_214387,RMVar_hsa_circ_214390 90467 RMVar_ID_90467 Human_SNP_ID_703975931 m1A Human chr22 - 39314177 39314177 39314177 GATTTATAAGATTGGCCAGGGCTACCTTATCAAGGACGGCAAGCTGATCAAGAACAATGCCTCCA GATTTATAAGATTGGCCAGGGCTACCTTATCAGGGACGGCAAGCTGATCAAGAACAATGCCTCCA T C RPL3 Ensembl:ENSG00000100316 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39314126..39314225 32194978 MeRIP-seq:(Medium) rs752844997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65199,Human_RBP_ID_580710,Human_RBP_ID_1029417,Human_RBP_ID_1201813,Human_RBP_ID_1612046,Human_RBP_ID_1943042,Human_RBP_ID_2728382,Human_RBP_ID_4712773,Human_RBP_ID_5203035,Human_RBP_ID_8117415,Human_RBP_ID_8550558,Human_RBP_ID_8863701,Human_RBP_ID_9126715,Human_RBP_ID_14489469,Human_RBP_ID_17986501,Human_RBP_ID_18329423,Human_RBP_ID_18445500,Human_RBP_ID_18535199,Human_RBP_ID_23948229 Human_Splice_Rec_2168102,Human_Splice_Rec_2168103,Human_Splice_Rec_2168120,Human_Splice_Rec_2168121,Human_Splice_Rec_2168142,Human_Splice_Rec_2168143,Human_Splice_Rec_2168150,Human_Splice_Rec_2168164,Human_Splice_Rec_2168165,Human_Splice_Rec_2168170 RMVar_hsa_circ_34133,RMVar_hsa_circ_92264,RMVar_hsa_circ_101826,RMVar_hsa_circ_214388,RMVar_hsa_circ_110607,RMVar_hsa_circ_214385,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_76609,RMVar_hsa_circ_214387,RMVar_hsa_circ_375411,RMVar_hsa_circ_214390,RMVar_hsa_circ_86228,RMVar_hsa_circ_214391,RMVar_hsa_circ_214392 90468 RMVar_ID_90468 Human_SNP_ID_703975932 m1A Human chr22 - 39314177 39314177 39314177 GATTTATAAGATTGGCCAGGGCTACCTTATCAAGGACGGCAAGCTGATCAAGAACAATGCCTCCA GATTTATAAGATTGGCCAGGGCTACCTTATCACGGACGGCAAGCTGATCAAGAACAATGCCTCCA T G RPL3 Ensembl:ENSG00000100316 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39314126..39314225 32194978 MeRIP-seq:(Medium) rs752844997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65199,Human_RBP_ID_580710,Human_RBP_ID_1029417,Human_RBP_ID_1201813,Human_RBP_ID_1612046,Human_RBP_ID_1943042,Human_RBP_ID_2728382,Human_RBP_ID_4712773,Human_RBP_ID_5203035,Human_RBP_ID_8117415,Human_RBP_ID_8550558,Human_RBP_ID_8863701,Human_RBP_ID_9126715,Human_RBP_ID_14489469,Human_RBP_ID_17986501,Human_RBP_ID_18329423,Human_RBP_ID_18445500,Human_RBP_ID_18535199,Human_RBP_ID_23948229 Human_Splice_Rec_2168102,Human_Splice_Rec_2168103,Human_Splice_Rec_2168120,Human_Splice_Rec_2168121,Human_Splice_Rec_2168142,Human_Splice_Rec_2168143,Human_Splice_Rec_2168150,Human_Splice_Rec_2168164,Human_Splice_Rec_2168165,Human_Splice_Rec_2168170 RMVar_hsa_circ_34133,RMVar_hsa_circ_92264,RMVar_hsa_circ_101826,RMVar_hsa_circ_214388,RMVar_hsa_circ_110607,RMVar_hsa_circ_214385,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_76609,RMVar_hsa_circ_214387,RMVar_hsa_circ_375411,RMVar_hsa_circ_214390,RMVar_hsa_circ_86228,RMVar_hsa_circ_214391,RMVar_hsa_circ_214392 90469 RMVar_ID_90469 Human_SNP_ID_703977042 m1A Human chr22 - 39316948 39316948 39316948 TTGCTGGTGGAAAAGGCTCCTTAGAAGCCGGCAATGAGCTCCATCCCCACGCGGTGCCAGTGTGC TTGCTGGTGGAAAAGGCTCCTTAGAAGCCGGCGATGAGCTCCATCCCCACGCGGTGCCAGTGTGC T C RPL3 Ensembl:ENSG00000100316 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39316947..39317148 32194978 MeRIP-seq:(Medium) rs776958654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4698643,Human_RBP_ID_9126721,Human_RBP_ID_9392994,Human_RBP_ID_27308362 Human_Splice_Rec_2168136,Human_Splice_Rec_2168200 Human_miRNA_ID_2726847 RMVar_hsa_circ_34133,RMVar_hsa_circ_101826,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_214387,RMVar_hsa_circ_375411,RMVar_hsa_circ_76935,RMVar_hsa_circ_13806,RMVar_hsa_circ_214392,RMVar_hsa_circ_92048,RMVar_hsa_circ_214393,RMVar_hsa_circ_86942,RMVar_hsa_circ_93986,RMVar_hsa_circ_84461,RMVar_hsa_circ_214394,RMVar_hsa_circ_214396,RMVar_hsa_circ_214397,RMVar_hsa_circ_214395 90470 RMVar_ID_90470 Human_SNP_ID_703977611 m1A Human chr22 - 39318312 39318312 39318312 GTAGAGATGGAGTCAAGCTGTTAGCAGAGGGCAGACTTTTTTTTTTAAGCAGGAGTTACACGTTG GTAGAGATGGAGTCAAGCTGTTAGCAGAGGGCCGACTTTTTTTTTTAAGCAGGAGTTACACGTTG T G RPL3 Ensembl:ENSG00000100316 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr22:39318309..39318439;chr22:39318311..39318468 26863196 MeRIP-seq:(Medium) rs1300100262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387405,Human_RBP_ID_7082874,Human_RBP_ID_10052374,Human_RBP_ID_14489652,Human_RBP_ID_18789533,Human_RBP_ID_23013674 RMVar_hsa_circ_101826,RMVar_hsa_circ_214386,RMVar_hsa_circ_375411,RMVar_hsa_circ_76935,RMVar_hsa_circ_13806,RMVar_hsa_circ_214392,RMVar_hsa_circ_86942,RMVar_hsa_circ_214396,RMVar_hsa_circ_214397 90471 RMVar_ID_90471 Human_SNP_ID_703977617 m1A Human chr22 - 39318338 39318338 39318338 AATAGGAGTGGAGGGGGAGGGAAATTGTAGAGATGGAGTCAAGCTGTTAGCAGAGGGCAGACTTT AATAGGAGTGGAGGGGGAGGGAAATTGTAGAGTTGGAGTCAAGCTGTTAGCAGAGGGCAGACTTT T A RPL3 Ensembl:ENSG00000100316 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:39318336..39318431 26863196 MeRIP-seq:(Medium) rs1295972333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5387405,Human_RBP_ID_14489654,Human_RBP_ID_18789533 RMVar_hsa_circ_101826,RMVar_hsa_circ_214386,RMVar_hsa_circ_375411,RMVar_hsa_circ_76935,RMVar_hsa_circ_13806,RMVar_hsa_circ_214392,RMVar_hsa_circ_86942,RMVar_hsa_circ_214396,RMVar_hsa_circ_214397 90472 RMVar_ID_90472 Human_SNP_ID_703977737 m1A Human chr22 + 39318549 39318549 39318549 CACGATGCCTGCTGCTGCGCTTCCGAGGCAGGAAGCCGAGGGACCCATGTCTGGGAGCGGAGAAC CACGATGCCTGCTGCTGCGCTTCCGAGGCAGGTAGCCGAGGGACCCATGTCTGGGAGCGGAGAAC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:39318451..39318625 26863410 MeRIP-seq:(Medium) rs1280990343 Functional Loss SNV dbSNP153 33..33 33 - - - 90473 RMVar_ID_90473 Human_SNP_ID_703977740 m1A Human chr22 + 39318559 39318559 39318559 GCTGCTGCGCTTCCGAGGCAGGAAGCCGAGGGACCCATGTCTGGGAGCGGAGAACTTTCTGTGAG GCTGCTGCGCTTCCGAGGCAGGAAGCCGAGGGCCCCATGTCTGGGAGCGGAGAACTTTCTGTGAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:39318476..39318625 26863410 MeRIP-seq:(Medium) rs1418605660 Functional Loss SNV dbSNP153 33..33 33 - - - 90474 RMVar_ID_90474 Human_SNP_ID_703978172 m1A Human chr22 - 39319476 39319476 39319476 GGCGCCGGGGGTTTGCTTTAGGGGCACGGGCGACCCAGCGGGGACTTCAGTCTGGCCTATTTTCT GGCGCCGGGGGTTTGCTTTAGGGGCACGGGCGGCCCAGCGGGGACTTCAGTCTGGCCTATTTTCT T C RPL3 Ensembl:ENSG00000100316 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39319456..39319625 26863196 MeRIP-seq:(Medium) rs538436245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929912,Human_RBP_ID_2719023,Human_RBP_ID_5389344,Human_RBP_ID_7082907,Human_RBP_ID_14489712,Human_RBP_ID_22086570,Human_RBP_ID_26789506 Human_Splice_Rec_2168153,Human_Splice_Rec_2168207,Human_Splice_Rec_2168213 RMVar_hsa_circ_76935,RMVar_hsa_circ_214397 90475 RMVar_ID_90475 Human_SNP_ID_703986816 m1A Human chr22 - 39350062 39350062 39350062 CAGGATGGTGTGCGGCTGCCGGACCAGGGTGTAGGGGTCGAAGGCGCCCCCGGCTTTGCCCGCTC CAGGATGGTGTGCGGCTGCCGGACCAGGGTGTTGGGGTCGAAGGCGCCCCCGGCTTTGCCCGCTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:39350012..39350150 26863196 MeRIP-seq:(Medium) rs750648147 Functional Loss SNV dbSNP153 33..33 33 - - - 90476 RMVar_ID_90476 Human_SNP_ID_703986817 m1A Human chr22 - 39350062 39350062 39350062 CAGGATGGTGTGCGGCTGCCGGACCAGGGTGTAGGGGTCGAAGGCGCCCCCGGCTTTGCCCGCTC CAGGATGGTGTGCGGCTGCCGGACCAGGGTGTCGGGGTCGAAGGCGCCCCCGGCTTTGCCCGCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:39350012..39350150 26863196 MeRIP-seq:(Medium) rs750648147 Functional Loss SNV dbSNP153 33..33 33 - - - 90477 RMVar_ID_90477 Human_SNP_ID_703995837 m1A Human chr22 - 39383358 39383358 39383358 TGGGTCACCTGCCACACTCTCCCCTACAGCCCATGGTCTTCCCTGGGCCTCCCATGCCTCAGGGG TGGGTCACCTGCCACACTCTCCCCTACAGCCCGTGGTCTTCCCTGGGCCTCCCATGCCTCAGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39383307..39383420 26863196 MeRIP-seq:(Medium) rs1241765244 Functional Loss SNV dbSNP153 33..33 33 - - - 90478 RMVar_ID_90478 Human_SNP_ID_704000219 m1A Human chr22 + 39399833 39399833 39399833 AGATGGCGGCGCAGAGGAGGAGCTTGCTGCAGAGTGTGAGGAACAGGCCCGCTCTCTGGGCTTGG AGATGGCGGCGCAGAGGAGGAGCTTGCTGCAGCGTGTGAGGAACAGGCCCGCTCTCTGGGCTTGG A C TAB1 Ensembl:ENSG00000100324 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:39399808..39399976;chr22:39399811..39399971 26863196 MeRIP-seq:(Medium) rs1023477773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708655 Human_Splice_Rec_2168251,Human_Splice_Rec_2168257,Human_Splice_Rec_2168277 RMVar_hsa_circ_109697,RMVar_hsa_circ_214399 90479 RMVar_ID_90479 Human_SNP_ID_704000220 m1A Human chr22 + 39399833 39399833 39399833 AGATGGCGGCGCAGAGGAGGAGCTTGCTGCAGAGTGTGAGGAACAGGCCCGCTCTCTGGGCTTGG AGATGGCGGCGCAGAGGAGGAGCTTGCTGCAGGGTGTGAGGAACAGGCCCGCTCTCTGGGCTTGG A G TAB1 Ensembl:ENSG00000100324 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:39399808..39399976;chr22:39399811..39399971 26863196 MeRIP-seq:(Medium) rs1023477773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708655 Human_Splice_Rec_2168251,Human_Splice_Rec_2168257,Human_Splice_Rec_2168277 RMVar_hsa_circ_109697,RMVar_hsa_circ_214399 90480 RMVar_ID_90480 Human_SNP_ID_704000245 m1A Human chr22 - 39399857 39399857 39399857 GCACCCCCGCCCAGGCTCCCAACCCCAAGCCCAGAGAGCGGGCCTGTTCCTCACACTCTGCAGCA GCACCCCCGCCCAGGCTCCCAACCCCAAGCCCGGAGAGCGGGCCTGTTCCTCACACTCTGCAGCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:39399809..39399974 26863196 MeRIP-seq:(Medium) rs748049481 Functional Loss SNV dbSNP153 33..33 33 - - - 90481 RMVar_ID_90481 Human_SNP_ID_704003869 m1A Human chr22 + 39414098 39414098 39414098 TGAGATCCTATGGGGTAGAATGGGCATTGCAGACAGGCAGGGATGCTGGAATCAGGGTGCCGTTG TGAGATCCTATGGGGTAGAATGGGCATTGCAGGCAGGCAGGGATGCTGGAATCAGGGTGCCGTTG A G TAB1 Ensembl:ENSG00000100324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:39414085..39414313;chr22:39414086..39414313 26863196 MeRIP-seq:(Medium) rs1230174014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14490056 RMVar_hsa_circ_109697,RMVar_hsa_circ_214399 90482 RMVar_ID_90482 Human_SNP_ID_704015668 m1A Human chr22 + 39457369 39457369 39457369 CCCCGGGACGGGGTGGAAGTGGGGGTGGGGGGAGGGGATCGGGGCCGGGCCGGGGCCGCGCTGCC CCCCGGGACGGGGTGGAAGTGGGGGTGGGGGGGGGGGATCGGGGCCGGGCCGGGGCCGCGCTGCC A G MGAT3 Ensembl:ENSG00000128268 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:39457285..39457372 26863410 MeRIP-seq:(Medium) rs1362921962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246150,Human_RBP_ID_3676126,Human_RBP_ID_5241251,Human_RBP_ID_9300411,Human_RBP_ID_9332859,Human_RBP_ID_9433220,Human_RBP_ID_18194129 RMVar_hsa_circ_100168,RMVar_hsa_circ_214404 90483 RMVar_ID_90483 Human_SNP_ID_704027560 m1A Human chr22 - 39502409 39502409 39502409 TCACCCGCAGGCCGTGCGCGCTACCACTCCGCAGGACTCGCCTCTGGCCGGGTACCTCTCCCCGG TCACCCGCAGGCCGTGCGCGCTACCACTCCGCCGGACTCGCCTCTGGCCGGGTACCTCTCCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39502358..39502463 26863196 MeRIP-seq:(Medium) rs1358686052 Functional Loss SNV dbSNP153 33..33 33 - - - 90484 RMVar_ID_90484 Human_SNP_ID_704028399 m1A Human chr22 - 39505681 39505680 39505681 ACTGCCACTGGTATGCTCCCTCTACGATACAAATGTGGCTATGTCATTCCTCTGTTTACAGAGCT ACTGCCACTGGTATGCTCCCTCTACGATACAA_TGTGGCTATGTCATTCCTCTGTTTACAGAGCT AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:39505672..39505959 26863196 MeRIP-seq:(Medium) rs1033910939 Functional Loss DEL dbSNP153 33..33 33 - - - 90485 RMVar_ID_90485 Human_SNP_ID_704028409 m1A Human chr22 + 39505732 39505732 39505732 ATACCAGTGGCAGTGTGAAGAATAAATTGATGAGAGATACTAGAGGCAGTGGATGTAGCCAGATC ATACCAGTGGCAGTGTGAAGAATAAATTGATGGGAGATACTAGAGGCAGTGGATGTAGCCAGATC A G MIEF1 Ensembl:ENSG00000100335 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39505724..39505976 26863196 MeRIP-seq:(Medium) rs1299583505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14490313 RMVar_hsa_circ_107542,RMVar_hsa_circ_123436,RMVar_hsa_circ_214407,RMVar_hsa_circ_214408 90486 RMVar_ID_90486 Human_SNP_ID_704030807 m1A Human chr22 + 39513992 39513992 39513992 CGCGGAGACGGCACGCCTGCGGGCTCTGGACCAGGCTGACTCGGGCTGCCGATCTCTGTGCCTCA CGCGGAGACGGCACGCCTGCGGGCTCTGGACCCGGCTGACTCGGGCTGCCGATCTCTGTGCCTCA A C MIEF1 Ensembl:ENSG00000100335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39513941..39514038 26863196 MeRIP-seq:(Medium) rs1203007810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245982,Human_RBP_ID_833934,Human_RBP_ID_7083002,Human_RBP_ID_8863765,Human_RBP_ID_9126750,Human_RBP_ID_9300725,Human_RBP_ID_14490444,Human_RBP_ID_17286082,Human_RBP_ID_22085358,Human_RBP_ID_27308483,Human_RBP_ID_27494288 RMVar_hsa_circ_107542,RMVar_hsa_circ_123436,RMVar_hsa_circ_214407,RMVar_hsa_circ_214408 90487 RMVar_ID_90487 Human_SNP_ID_704032727 m1A Human chr22 - 39520621 39520621 39520621 CGCCATGGTGGCCGTGGACCCTGAGGGCGGGGAGGAGGGAAAACGCACACGCGCAGAGAAAACTA CGCCATGGTGGCCGTGGACCCTGAGGGCGGGGGGGAGGGAAAACGCACACGCGCAGAGAAAACTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:39520551..39521186;chr22:39520551..39520803 26863196 MeRIP-seq:(Medium) rs1223631279 Functional Loss SNV dbSNP153 33..33 33 - - - 90488 RMVar_ID_90488 Human_SNP_ID_704032741 m1A Human chr22 + 39520632 39520632 39520632 GCGCGTGTGCGTTTTCCCTCCTCCCCGCCCTCAGGGTCCACGGCCACCATGGCGTATTAGGGGCA GCGCGTGTGCGTTTTCCCTCCTCCCCGCCCTCGGGGTCCACGGCCACCATGGCGTATTAGGGGCA A G ATF4 Ensembl:ENSG00000128272 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr22:39520576..39520775 26863196,32194978 MeRIP-seq:(Medium) rs1481078225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246152,Human_RBP_ID_580906,Human_RBP_ID_781516,Human_RBP_ID_833445,Human_RBP_ID_932102,Human_RBP_ID_1101589,Human_RBP_ID_4709073,Human_RBP_ID_5119937,Human_RBP_ID_5504872,Human_RBP_ID_7083111,Human_RBP_ID_9126764,Human_RBP_ID_17399847,Human_RBP_ID_17515836,Human_RBP_ID_22087184,Human_RBP_ID_23948512,Human_RBP_ID_26501526,Human_RBP_ID_27038221,Human_RBP_ID_27308525 Human_miRNA_ID_1974044,Human_miRNA_ID_1976224,Human_miRNA_ID_2614012 RMVar_hsa_circ_104510,RMVar_hsa_circ_214409 90489 RMVar_ID_90489 Human_SNP_ID_704032742 m1A Human chr22 + 39520632 39520632 39520632 GCGCGTGTGCGTTTTCCCTCCTCCCCGCCCTCAGGGTCCACGGCCACCATGGCGTATTAGGGGCA GCGCGTGTGCGTTTTCCCTCCTCCCCGCCCTCTGGGTCCACGGCCACCATGGCGTATTAGGGGCA A T ATF4 Ensembl:ENSG00000128272 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr22:39520576..39520775 26863196,32194978 MeRIP-seq:(Medium) rs1481078225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246152,Human_RBP_ID_580906,Human_RBP_ID_781516,Human_RBP_ID_833445,Human_RBP_ID_932102,Human_RBP_ID_1101589,Human_RBP_ID_4709073,Human_RBP_ID_5119937,Human_RBP_ID_5504872,Human_RBP_ID_7083111,Human_RBP_ID_9126764,Human_RBP_ID_17399847,Human_RBP_ID_17515836,Human_RBP_ID_22087184,Human_RBP_ID_23948512,Human_RBP_ID_26501526,Human_RBP_ID_27038221,Human_RBP_ID_27308525 Human_miRNA_ID_1974044,Human_miRNA_ID_1976224,Human_miRNA_ID_2614012 RMVar_hsa_circ_104510,RMVar_hsa_circ_214409 90490 RMVar_ID_90490 Human_SNP_ID_704032764 m1A Human chr22 + 39520721 39520697 39520721 TTTGCAGCGGCGGCAGCAGCACCAGGCTCTGCAGCGGCAACCCCCAGCGGCTTAAGCCATGGCGT TTTGCAGCG________________________GCGGCAACCCCCAGCGGCTTAAGCCATGGCGT GGCGGCAGCAGCACCAGGCTCTGCA G ATF4 Ensembl:ENSG00000128272 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:39520551..39520800 26863410 MeRIP-seq:(Medium) rs1457935280 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_246153,Human_RBP_ID_580908,Human_RBP_ID_781517,Human_RBP_ID_1029466,Human_RBP_ID_1612170,Human_RBP_ID_4709074,Human_RBP_ID_5120098,Human_RBP_ID_7083114,Human_RBP_ID_8550676,Human_RBP_ID_8863851,Human_RBP_ID_17286108,Human_RBP_ID_17399298,Human_RBP_ID_18789600,Human_RBP_ID_22087003,Human_RBP_ID_22508101 Human_Splice_Rec_2168409,Human_Splice_Rec_2168415 Human_miRNA_ID_2686649 RMVar_hsa_circ_104510,RMVar_hsa_circ_214409 90491 RMVar_ID_90491 Human_SNP_ID_704032804 m1A Human chr22 - 39520804 39520804 39520804 CGCCCTGGCCCCAGGCCGCACCCCACCAATCCAAAACCCGCGCCGGCCCCAGGAGCACAGCTGGA CGCCCTGGCCCCAGGCCGCACCCCACCAATCCGAAACCCGCGCCGGCCCCAGGAGCACAGCTGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:39520801..39520825 26863196 MeRIP-seq:(Medium) rs561280964 Functional Loss SNV dbSNP153 33..33 33 - - - 90492 RMVar_ID_90492 Human_SNP_ID_704033366 m1A Human chr22 + 39521908 39521908 39521908 TGACCTTCTGACCACGTTGGATGACACTTGTGATCTCTTTGCCCCCCTAGTCCAGGAGACTAATA TGACCTTCTGACCACGTTGGATGACACTTGTGTTCTCTTTGCCCCCCTAGTCCAGGAGACTAATA A T ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:39521489..39522200 26863196 MeRIP-seq:(Medium) rs759424161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580923,Human_RBP_ID_781521,Human_RBP_ID_1029474,Human_RBP_ID_1382734,Human_RBP_ID_1612182,Human_RBP_ID_1943105,Human_RBP_ID_3673110,Human_RBP_ID_7083126,Human_RBP_ID_8550686,Human_RBP_ID_9126770,Human_RBP_ID_9392369,Human_RBP_ID_14490686,Human_RBP_ID_17286114,Human_RBP_ID_17515305,Human_RBP_ID_18168873,Human_RBP_ID_18789612,Human_RBP_ID_22087189,Human_RBP_ID_22821017,Human_RBP_ID_23948522,Human_RBP_ID_26501535,Human_RBP_ID_27038247,Human_RBP_ID_27308539,Human_RBP_ID_27494331 Human_miRNA_ID_2546461,Human_miRNA_ID_2546462,Human_miRNA_ID_2780367,Human_miRNA_ID_2780368 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90493 RMVar_ID_90493 Human_SNP_ID_704033395 m1A Human chr22 + 39521944 39521944 39521944 CTTTGCCCCCCTAGTCCAGGAGACTAATAAGCAGCCCCCCCAGACGGTGAACCCAATTGGCCATC CTTTGCCCCCCTAGTCCAGGAGACTAATAAGCGGCCCCCCCAGACGGTGAACCCAATTGGCCATC A G ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr22:39521795..39522162;chr22:39521901..39522075;chr22:39521901..39521975 31548705,26863196 m1A-IP-seq:(High) rs146469032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65474,Human_RBP_ID_246158,Human_RBP_ID_580924,Human_RBP_ID_781522,Human_RBP_ID_932109,Human_RBP_ID_1029475,Human_RBP_ID_1612186,Human_RBP_ID_1943106,Human_RBP_ID_4712908,Human_RBP_ID_5119939,Human_RBP_ID_7083132,Human_RBP_ID_8550690,Human_RBP_ID_9126770,Human_RBP_ID_14490694,Human_RBP_ID_17286116,Human_RBP_ID_17399302,Human_RBP_ID_17986637,Human_RBP_ID_22087189,Human_RBP_ID_22270629,Human_RBP_ID_22508106,Human_RBP_ID_22821018,Human_RBP_ID_23016201,Human_RBP_ID_23948526,Human_RBP_ID_25671310,Human_RBP_ID_26501122,Human_RBP_ID_27038248,Human_RBP_ID_27308541,Human_RBP_ID_27494333 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90494 RMVar_ID_90494 Human_SNP_ID_704033427 m1A Human chr22 + 39521985 39521985 39521985 AGACGGTGAACCCAATTGGCCATCTCCCAGAAAGTTTAACAAAACCCGACCAGGTTGCCCCCTTC AGACGGTGAACCCAATTGGCCATCTCCCAGAAGGTTTAACAAAACCCGACCAGGTTGCCCCCTTC A G ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:39521935..39522078 26863196 MeRIP-seq:(Medium) rs377487629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580924,Human_RBP_ID_1308006,Human_RBP_ID_1943106,Human_RBP_ID_5119940,Human_RBP_ID_14490694,Human_RBP_ID_18789614,Human_RBP_ID_20764270,Human_RBP_ID_22821019,Human_RBP_ID_26501537 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90495 RMVar_ID_90495 Human_SNP_ID_704033457 m1A Human chr22 + 39522028 39522028 39522028 ACCCGACCAGGTTGCCCCCTTCACCTTCTTACAACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT ACCCGACCAGGTTGCCCCCTTCACCTTCTTACCACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT A C ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:39521905..39522130 26863196 MeRIP-seq:(Medium) rs552162021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580932,Human_RBP_ID_781523,Human_RBP_ID_1612190,Human_RBP_ID_2719080,Human_RBP_ID_3673111,Human_RBP_ID_5119941,Human_RBP_ID_5424538,Human_RBP_ID_5446580,Human_RBP_ID_5473185,Human_RBP_ID_5504874,Human_RBP_ID_7083134,Human_RBP_ID_8117433,Human_RBP_ID_8207966,Human_RBP_ID_8262374,Human_RBP_ID_8550692,Human_RBP_ID_17020878,Human_RBP_ID_17286117,Human_RBP_ID_17399304,Human_RBP_ID_17515307,Human_RBP_ID_17986638,Human_RBP_ID_18201485,Human_RBP_ID_18516432,Human_RBP_ID_18953053,Human_RBP_ID_20764270,Human_RBP_ID_21937790,Human_RBP_ID_22085393,Human_RBP_ID_22270630,Human_RBP_ID_22821019,Human_RBP_ID_23285656,Human_RBP_ID_23948527,Human_RBP_ID_24494359,Human_RBP_ID_26498709,Human_RBP_ID_27038250,Human_RBP_ID_27308542,Human_RBP_ID_27494336,Human_RBP_ID_27565389 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90496 RMVar_ID_90496 Human_SNP_ID_704033458 m1A Human chr22 + 39522028 39522028 39522028 ACCCGACCAGGTTGCCCCCTTCACCTTCTTACAACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT ACCCGACCAGGTTGCCCCCTTCACCTTCTTACGACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT A G ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:39521905..39522130 26863196 MeRIP-seq:(Medium) rs552162021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580932,Human_RBP_ID_781523,Human_RBP_ID_1612190,Human_RBP_ID_2719080,Human_RBP_ID_3673111,Human_RBP_ID_5119941,Human_RBP_ID_5424538,Human_RBP_ID_5446580,Human_RBP_ID_5473185,Human_RBP_ID_5504874,Human_RBP_ID_7083134,Human_RBP_ID_8117433,Human_RBP_ID_8207966,Human_RBP_ID_8262374,Human_RBP_ID_8550692,Human_RBP_ID_17020878,Human_RBP_ID_17286117,Human_RBP_ID_17399304,Human_RBP_ID_17515307,Human_RBP_ID_17986638,Human_RBP_ID_18201485,Human_RBP_ID_18516432,Human_RBP_ID_18953053,Human_RBP_ID_20764270,Human_RBP_ID_21937790,Human_RBP_ID_22085393,Human_RBP_ID_22270630,Human_RBP_ID_22821019,Human_RBP_ID_23285656,Human_RBP_ID_23948527,Human_RBP_ID_24494359,Human_RBP_ID_26498709,Human_RBP_ID_27038250,Human_RBP_ID_27308542,Human_RBP_ID_27494336,Human_RBP_ID_27565389 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90497 RMVar_ID_90497 Human_SNP_ID_704033595 m1A Human chr22 + 39522249 39522249 39522249 GCCCAGAGTCCTATCTGGGGTCTCCTCAGCACAGCCCCTCTACCAGGGGCTCTCCAAATAGGAGC GCCCAGAGTCCTATCTGGGGTCTCCTCAGCACGGCCCCTCTACCAGGGGCTCTCCAAATAGGAGC A G ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:39522191..39522375 32194978 MeRIP-seq:(Medium) rs770110284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580939,Human_RBP_ID_781526,Human_RBP_ID_1029479,Human_RBP_ID_1242320,Human_RBP_ID_1612195,Human_RBP_ID_5324788,Human_RBP_ID_17286122,Human_RBP_ID_17399853,Human_RBP_ID_17515309,Human_RBP_ID_17986641,Human_RBP_ID_27038256 Human_miRNA_ID_466213,Human_miRNA_ID_1561371,Human_miRNA_ID_2391485,Human_miRNA_ID_2391486,Human_miRNA_ID_2437442,Human_miRNA_ID_2437443,Human_miRNA_ID_2592726,Human_miRNA_ID_2592727 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90498 RMVar_ID_90498 Human_SNP_ID_704033596 m1A Human chr22 + 39522249 39522249 39522249 GCCCAGAGTCCTATCTGGGGTCTCCTCAGCACAGCCCCTCTACCAGGGGCTCTCCAAATAGGAGC GCCCAGAGTCCTATCTGGGGTCTCCTCAGCACTGCCCCTCTACCAGGGGCTCTCCAAATAGGAGC A T ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:39522191..39522375 32194978 MeRIP-seq:(Medium) rs770110284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580939,Human_RBP_ID_781526,Human_RBP_ID_1029479,Human_RBP_ID_1242320,Human_RBP_ID_1612195,Human_RBP_ID_5324788,Human_RBP_ID_17286122,Human_RBP_ID_17399853,Human_RBP_ID_17515309,Human_RBP_ID_17986641,Human_RBP_ID_27038256 Human_miRNA_ID_466213,Human_miRNA_ID_1561371,Human_miRNA_ID_2391485,Human_miRNA_ID_2391486,Human_miRNA_ID_2437442,Human_miRNA_ID_2437443,Human_miRNA_ID_2592726,Human_miRNA_ID_2592727 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 90499 RMVar_ID_90499 Human_SNP_ID_704046044 m1A Human chr22 + 39566089 39566083 39566089 TGATGGTGGTGGTGATGGTGATGATGGTGTTGATGGTGATGATGGTGTTGGTGGTGGTGATGGTG TGATGGTGGTGGTGATGGTGATGATGG______TGGTGATGATGGTGTTGGTGGTGGTGATGGTG GTGTTGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39566068..39566133 26863196 MeRIP-seq:(Medium) rs1191067762 Functional Loss DEL dbSNP153 28..33 33 - - - 90500 RMVar_ID_90500 Human_SNP_ID_704046053 m1A Human chr22 + 39566089 39566089 39566089 TGATGGTGGTGGTGATGGTGATGATGGTGTTGATGGTGATGATGGTGTTGGTGGTGGTGATGGTG TGATGGTGGTGGTGATGGTGATGATGGTGTTGGTGGTGATGATGGTGTTGGTGGTGGTGATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39566068..39566133 26863196 MeRIP-seq:(Medium) rs1450861947 Functional Loss SNV dbSNP153 33..33 33 - - - 90501 RMVar_ID_90501 Human_SNP_ID_500744272 m1A Human chr12 - 50016715 50016715 50016715 CCCTAATGTATATTTGATTTCTTGGCAGAAAGATGGATACTATGATGCTGAATGTGCGGAATCTG CCCTAATGTATATTTGATTTCTTGGCAGAAAGGTGGATACTATGATGCTGAATGTGCGGAATCTG T C RACGAP1 Ensembl:ENSG00000161800 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:50016573..50016750 26863410 MeRIP-seq:(Medium) rs1343914376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11960137,Human_RBP_ID_22572532,Human_RBP_ID_23562594 Human_Splice_Rec_1367142,Human_Splice_Rec_1367143,Human_Splice_Rec_1367174,Human_Splice_Rec_1367175,Human_Splice_Rec_1367206,Human_Splice_Rec_1367207,Human_Splice_Rec_1367237,Human_Splice_Rec_1367272,Human_Splice_Rec_1367273,Human_Splice_Rec_1367336,Human_Splice_Rec_1367337,Human_Splice_Rec_1367348,Human_Splice_Rec_1367349,Human_Splice_Rec_1367370,Human_Splice_Rec_1367371,Human_Splice_Rec_1367382,Human_Splice_Rec_1367383,Human_Splice_Rec_1367410,Human_Splice_Rec_1367411,Human_Splice_Rec_1367420,Human_Splice_Rec_1367421,Human_Splice_Rec_1367430,Human_Splice_Rec_1367431,Human_Splice_Rec_1367438,Human_Splice_Rec_1367439,Human_Splice_Rec_1367446,Human_Splice_Rec_1367447,Human_Splice_Rec_1367460,Human_Splice_Rec_1367461,Human_Splice_Rec_1367466,Human_Splice_Rec_1367467,Human_Splice_Rec_1367472,Human_Splice_Rec_1367473,Human_Splice_Rec_1367480,Human_Splice_Rec_1367481,Human_Splice_Rec_1367488,Human_Splice_Rec_1367489,Human_Splice_Rec_1367496,Human_Splice_Rec_1367497 Human_miRNA_ID_3063023 RMVar_hsa_circ_77098,RMVar_hsa_circ_125613,RMVar_hsa_circ_38912,RMVar_hsa_circ_68956,RMVar_hsa_circ_156379,RMVar_hsa_circ_312022,RMVar_hsa_circ_53776,RMVar_hsa_circ_156381,RMVar_hsa_circ_156380,RMVar_hsa_circ_43019,RMVar_hsa_circ_56485,RMVar_hsa_circ_32453,RMVar_hsa_circ_24576,RMVar_hsa_circ_356050,RMVar_hsa_circ_156394,RMVar_hsa_circ_101053,RMVar_hsa_circ_334636,RMVar_hsa_circ_117200,RMVar_hsa_circ_156396,RMVar_hsa_circ_156397,RMVar_hsa_circ_332903,RMVar_hsa_circ_156398,RMVar_hsa_circ_298346 90502 RMVar_ID_90502 Human_SNP_ID_500746229 m1A Human chr12 + 50025355 50025355 50025355 CTCACCACACGAACACTCTGCTTCCTATCACAATCCAGCGGCAGACGCACCTGGTCTGGCACCCC CTCACCACACGAACACTCTGCTTCCTATCACAGTCCAGCGGCAGACGCACCTGGTCTGGCACCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:50025308..50025439 26863196 MeRIP-seq:(Medium) rs966471883 Functional Loss SNV dbSNP153 33..33 33 - - - 90503 RMVar_ID_90503 Human_SNP_ID_500755568 m1A Human chr12 + 50064207 50064207 50064207 GGGAAGGGTTCCTGCCCTAGGGGTTCATGGCTACCACCTCCTGCCTTATCCTTCTCATCTGTCCC GGGAAGGGTTCCTGCCCTAGGGGTTCATGGCTGCCACCTCCTGCCTTATCCTTCTCATCTGTCCC A G ASIC1 Ensembl:ENSG00000110881 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:50064204..50064333 32194978 MeRIP-seq:(Medium) rs1005716418 Functional Loss SNV dbSNP153 33..33 33 - - - 90504 RMVar_ID_90504 Human_SNP_ID_500757165 m1A Human chr12 + 50071061 50071061 50071061 AGGGCCTTGAGCAGAACTGGACCCTTTAGTCTATTCCCTGGGTGGGCACTAACAGCACCCTGTGG AGGGCCTTGAGCAGAACTGGACCCTTTAGTCTGTTCCCTGGGTGGGCACTAACAGCACCCTGTGG A G ASIC1 Ensembl:ENSG00000110881 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50071052..50071177 26863196 MeRIP-seq:(Medium) rs1043331534 Functional Loss SNV dbSNP153 33..33 33 - - - 90505 RMVar_ID_90505 Human_SNP_ID_500760821 m1A Human chr12 - 50085262 50085262 50085262 CGCCCGCCTGTTCCCCCGGCCGGCCGGCCGGCACGGGAGGCTCAGGGCAGCGAGACTATGGGATA CGCCCGCCTGTTCCCCCGGCCGGCCGGCCGGCTCGGGAGGCTCAGGGCAGCGAGACTATGGGATA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:50085226..50085473 26863196 MeRIP-seq:(Medium) rs1427905433 Functional Loss SNV dbSNP153 33..33 33 - - - 90506 RMVar_ID_90506 Human_SNP_ID_500760822 m1A Human chr12 - 50085262 50085262 50085262 CGCCCGCCTGTTCCCCCGGCCGGCCGGCCGGCACGGGAGGCTCAGGGCAGCGAGACTATGGGATA CGCCCGCCTGTTCCCCCGGCCGGCCGGCCGGCCCGGGAGGCTCAGGGCAGCGAGACTATGGGATA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:50085226..50085473 26863196 MeRIP-seq:(Medium) rs1427905433 Functional Loss SNV dbSNP153 33..33 33 - - - 90507 RMVar_ID_90507 Human_SNP_ID_500764066 m1A Human chr12 - 50096974 50096974 50096974 CTAAGTCCCTTCAGACCTCTCCTAGGTTCTTTACCTTGAGGTCCCTGCACTGGGACTGAAGCCAG CTAAGTCCCTTCAGACCTCTCCTAGGTTCTTTGCCTTGAGGTCCCTGCACTGGGACTGAAGCCAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:50096901..50097065 26863196 MeRIP-seq:(Medium) rs1281983969 Functional Loss SNV dbSNP153 33..33 33 - - - 90508 RMVar_ID_90508 Human_SNP_ID_500770461 m1A Human chr12 + 50120044 50120040 50120044 TCTAAATTCAATCTGTCTTTGTAGGGGACAAGATGCCAACTGGCAAGCAGCTAGCTGACATTGGC TCTAAATTCAATCTGTCTTTGTAGGGGAC____TGCCAACTGGCAAGCAGCTAGCTGACATTGGC CAAGA C AC074032.1,COX14 Ensembl:ENSG00000272368,Ensembl:ENSG00000178449 lincRNA,Protein coding intron,start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:50120026..50120075 26863196 MeRIP-seq:(Medium) rs1259051091 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_4226365,Human_RBP_ID_5558231 Human_Splice_Rec_1367822,Human_Splice_Rec_1367826,Human_Splice_Rec_1367828,Human_Splice_Rec_1367830 RMVar_hsa_circ_103065,RMVar_hsa_circ_123401,RMVar_hsa_circ_156406,RMVar_hsa_circ_156407 90509 RMVar_ID_90509 Human_SNP_ID_500782535 m1A Human chr12 + 50167296 50167296 50167296 GCAAGCTTAGGGGTCCCTGCGCTGCTGTCGCCATCTTACGCCCACCCCGAAGCCACCGCCGCCAC GCAAGCTTAGGGGTCCCTGCGCTGCTGTCGCCGTCTTACGCCCACCCCGAAGCCACCGCCGCCAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:50167209..50167302 26863410 MeRIP-seq:(Medium) rs779387416 Functional Loss SNV dbSNP153 33..33 33 - - - 90510 RMVar_ID_90510 Human_SNP_ID_500786836 m1A Human chr12 - 50181911 50181911 50181911 TCAGCTGCTTCCGTTGCTCCTATTGCAACAACAAACTCAGGTAAGTCAGCCCAAAACAAGCCATC TCAGCTGCTTCCGTTGCTCCTATTGCAACAACGAACTCAGGTAAGTCAGCCCAAAACAAGCCATC T C LIMA1 Ensembl:ENSG00000050405 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:50181909..50182059 32194978 MeRIP-seq:(Medium) rs747973365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18628106 Human_Splice_Rec_1368075,Human_Splice_Rec_1368083,Human_Splice_Rec_1368097,Human_Splice_Rec_1368117,Human_Splice_Rec_1368137,Human_Splice_Rec_1368151,Human_Splice_Rec_1368165,Human_Splice_Rec_1368187,Human_Splice_Rec_1368189,Human_Splice_Rec_1368195 RMVar_hsa_circ_156423,RMVar_hsa_circ_267719,RMVar_hsa_circ_330192,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_334061,RMVar_hsa_circ_313701,RMVar_hsa_circ_156422 90511 RMVar_ID_90511 Human_SNP_ID_500789421 m1A Human chr12 - 50192552 50192552 50192552 TCTTCCTTTTGTAACTCAAGCAGGTGACTCCCAGGTTAAGAGTGAGGTTCAACAGCCTGTCCATC TCTTCCTTTTGTAACTCAAGCAGGTGACTCCCGGGTTAAGAGTGAGGTTCAACAGCCTGTCCATC T C LIMA1 Ensembl:ENSG00000050405 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:50192470..50195623 32194978 MeRIP-seq:(Medium) rs771394825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_873638,Human_RBP_ID_2341059 Human_Splice_Rec_1368072,Human_Splice_Rec_1368080,Human_Splice_Rec_1368094,Human_Splice_Rec_1368114,Human_Splice_Rec_1368134,Human_Splice_Rec_1368148,Human_Splice_Rec_1368162,Human_Splice_Rec_1368182,Human_Splice_Rec_1368208 RMVar_hsa_circ_5462,RMVar_hsa_circ_156423,RMVar_hsa_circ_267719,RMVar_hsa_circ_330192,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_334061,RMVar_hsa_circ_313701,RMVar_hsa_circ_112210,RMVar_hsa_circ_361218,RMVar_hsa_circ_156422,RMVar_hsa_circ_313075,RMVar_hsa_circ_15695,RMVar_hsa_circ_156424 90512 RMVar_ID_90512 Human_SNP_ID_500796837 m1A Human chr12 - 50222554 50222554 50222554 CAGGAGCAGCTTGGAGTTTTAACTTTCATTTTACAAAGAACAACATGTTTGAATGTTTCAGCAGG CAGGAGCAGCTTGGAGTTTTAACTTTCATTTTGCAAAGAACAACATGTTTGAATGTTTCAGCAGG T C LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50222509..50222601 26863196 MeRIP-seq:(Medium) rs754116242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36332,Human_RBP_ID_1796367,Human_RBP_ID_6192723,Human_RBP_ID_11962569 RMVar_hsa_circ_264925,RMVar_hsa_circ_156425,RMVar_hsa_circ_288627,RMVar_hsa_circ_300816 90513 RMVar_ID_90513 Human_SNP_ID_500810949 m1A Human chr12 - 50283495 50283495 50283495 CAGGAGCAGTAGGTGTTAGCAGCTTGGTCGCGACAGGTGCGCTAGGTAGAGCGCCGGGACCTGTG CAGGAGCAGTAGGTGTTAGCAGCTTGGTCGCGGCAGGTGCGCTAGGTAGAGCGCCGGGACCTGTG T C LIMA1 Ensembl:ENSG00000050405 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50283391..50283505 26863196 MeRIP-seq:(Medium) rs1285787052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247439,Human_RBP_ID_17820944 Human_Splice_Rec_1368099,Human_Splice_Rec_1368119,Human_Splice_Rec_1368167,Human_Splice_Rec_1368217 90514 RMVar_ID_90514 Human_SNP_ID_500840823 m1A Human chr12 + 50400985 50400985 50400985 GCCTGTGAGCCAGTTGGAGTTGCGGCGGCGGGAACGATTGGGCTGAGCAGAGGACGACATGTTGC GCCTGTGAGCCAGTTGGAGTTGCGGCGGCGGGGACGATTGGGCTGAGCAGAGGACGACATGTTGC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:50400876..50401151 26863196 MeRIP-seq:(Medium) rs575463540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36897,Human_RBP_ID_230068,Human_RBP_ID_4246651,Human_RBP_ID_5171663,Human_RBP_ID_5560974,Human_RBP_ID_6192842,Human_RBP_ID_9366359,Human_RBP_ID_19056149,Human_RBP_ID_23125625,Human_RBP_ID_23562959 Human_Splice_Rec_1368277,Human_Splice_Rec_1368305,Human_Splice_Rec_1368335,Human_Splice_Rec_1368365,Human_Splice_Rec_1368371,Human_Splice_Rec_1368379,Human_Splice_Rec_1368391,Human_Splice_Rec_1368417,Human_Splice_Rec_1368437,Human_Splice_Rec_1368449,Human_Splice_Rec_1368479,Human_Splice_Rec_1368487,Human_Splice_Rec_1368495,Human_Splice_Rec_1368517,Human_Splice_Rec_1368545 90515 RMVar_ID_90515 Human_SNP_ID_500840827 m1A Human chr12 - 50400990 50400990 50400990 GAAAAGCAACATGTCGTCCTCTGCTCAGCCCAATCGTTCCCGCCGCCGCAACTCCAACTGGCTCA GAAAAGCAACATGTCGTCCTCTGCTCAGCCCAGTCGTTCCCGCCGCCGCAACTCCAACTGGCTCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:50400904..50401061 26863196 MeRIP-seq:(Medium) rs749168180 Functional Loss SNV dbSNP153 33..33 33 - - - 90516 RMVar_ID_90516 Human_SNP_ID_500840830 m1A Human chr12 - 50400996 50400996 50400996 CTCCACGAAAAGCAACATGTCGTCCTCTGCTCAGCCCAATCGTTCCCGCCGCCGCAACTCCAACT CTCCACGAAAAGCAACATGTCGTCCTCTGCTCGGCCCAATCGTTCCCGCCGCCGCAACTCCAACT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:50400865..50401050 26863196 MeRIP-seq:(Medium) rs1357351173 Functional Loss SNV dbSNP153 33..33 33 - - - 90517 RMVar_ID_90517 Human_SNP_ID_500860553 m1A Human chr12 + 50475983 50475983 50475983 TAGCCAGGAAGGAAACAAGAGAAAGTACGTCCATTTCATTATGGATTTTGGAGTTGTGAGTGATA TAGCCAGGAAGGAAACAAGAGAAAGTACGTCCGTTTCATTATGGATTTTGGAGTTGTGAGTGATA A G LARP4 Ensembl:ENSG00000161813 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:50475901..50476008 32194978 MeRIP-seq:(Medium) rs1450075797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421464,Human_RBP_ID_8782517,Human_RBP_ID_23563099,Human_RBP_ID_27630129 Human_miRNA_ID_644622,Human_miRNA_ID_1656870 90518 RMVar_ID_90518 Human_SNP_ID_500867938 m1A Human chr12 - 50505157 50505157 50505157 GCAGCGCCGCCACCGCGGCCGGCGACGGCTCCAGGCCTCGTTCCGCCATCCCAGCTCCGCCAGCC GCAGCGCCGCCACCGCGGCCGGCGACGGCTCCCGGCCTCGTTCCGCCATCCCAGCTCCGCCAGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:50505022..50505299 26863196 MeRIP-seq:(Medium) rs1006771450 Functional Loss SNV dbSNP153 33..33 33 - - - 90519 RMVar_ID_90519 Human_SNP_ID_500867953 m1A Human chr12 - 50505178 50505178 50505178 GCTGCGCCCGCACTTCAGGCGGCAGCGCCGCCACCGCGGCCGGCGACGGCTCCAGGCCTCGTTCC GCTGCGCCCGCACTTCAGGCGGCAGCGCCGCCTCCGCGGCCGGCGACGGCTCCAGGCCTCGTTCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr12:50505051..50505275;chr12:50505014..50640757 26863196 MeRIP-seq:(Medium) rs547240228 Functional Loss SNV dbSNP153 33..33 33 - - - 90520 RMVar_ID_90520 Human_SNP_ID_500867954 m1A Human chr12 - 50505178 50505178 50505178 GCTGCGCCCGCACTTCAGGCGGCAGCGCCGCCACCGCGGCCGGCGACGGCTCCAGGCCTCGTTCC GCTGCGCCCGCACTTCAGGCGGCAGCGCCGCCCCCGCGGCCGGCGACGGCTCCAGGCCTCGTTCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr12:50505051..50505275;chr12:50505014..50640757 26863196 MeRIP-seq:(Medium) rs547240228 Functional Loss SNV dbSNP153 33..33 33 - - - 90521 RMVar_ID_90521 Human_SNP_ID_500913255 m1A Human chr12 + 50689715 50689715 50689715 TTAGTTGACTCTGTCAGTCTGGATCTCTCTGGAGGAGAGGCTGGGTTGAAGATAGAGAACAAGGA TTAGTTGACTCTGTCAGTCTGGATCTCTCTGGTGGAGAGGCTGGGTTGAAGATAGAGAACAAGGA A T DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50689700..50689862 26863196 MeRIP-seq:(Medium) rs962697738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_156475,RMVar_hsa_circ_86435,RMVar_hsa_circ_110970,RMVar_hsa_circ_377502,RMVar_hsa_circ_338486,RMVar_hsa_circ_46636,RMVar_hsa_circ_37183,RMVar_hsa_circ_156482,RMVar_hsa_circ_1099,RMVar_hsa_circ_33446,RMVar_hsa_circ_27406,RMVar_hsa_circ_156490,RMVar_hsa_circ_268262,RMVar_hsa_circ_265421,RMVar_hsa_circ_266917,RMVar_hsa_circ_343698,RMVar_hsa_circ_333848,RMVar_hsa_circ_264861,RMVar_hsa_circ_31160,RMVar_hsa_circ_49631,RMVar_hsa_circ_156492,RMVar_hsa_circ_36057,RMVar_hsa_circ_53522,RMVar_hsa_circ_156493,RMVar_hsa_circ_275473,RMVar_hsa_circ_331582,RMVar_hsa_circ_363688,RMVar_hsa_circ_323755,RMVar_hsa_circ_278854,RMVar_hsa_circ_95819,RMVar_hsa_circ_102819,RMVar_hsa_circ_53409,RMVar_hsa_circ_156495,RMVar_hsa_circ_31651,RMVar_hsa_circ_35419,RMVar_hsa_circ_156497,RMVar_hsa_circ_156499,RMVar_hsa_circ_156498,RMVar_hsa_circ_156496,RMVar_hsa_circ_80709,RMVar_hsa_circ_156494,RMVar_hsa_circ_350618,RMVar_hsa_circ_33313,RMVar_hsa_circ_156501 90522 RMVar_ID_90522 Human_SNP_ID_500926613 m1A Human chr12 - 50745902 50745902 50745902 CTCGTGAACTGGAAGAACAGAGGACACTCCTCAGTTTTCAGAAGAGAAGTTATATGGATAAACTG CTCGTGAACTGGAAGAACAGAGGACACTCCTCCGTTTTCAGAAGAGAAGTTATATGGATAAACTG T G lnc-SLC11A2-8 RNACentral:URS0000D5E087 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:50745851..50745964 32194978 MeRIP-seq:(Medium) rs1179069914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156529 90523 RMVar_ID_90523 Human_SNP_ID_500931371 m1A Human chr12 - 50764151 50764151 50764151 GTCAGGCGGGGCGGGGAGAATCAGTGTCACTTAACAGCCAACTGTCCTAAGCTACCGTTTCCTCG GTCAGGCGGGGCGGGGAGAATCAGTGTCACTTCACAGCCAACTGTCCTAAGCTACCGTTTCCTCG T G lnc-SLC11A2-8 RNACentral:URS0000D5E087 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50764101..50764517 26863196 MeRIP-seq:(Medium) rs1371161672 Functional Loss SNV dbSNP153 33..33 33 - - - 90524 RMVar_ID_90524 Human_SNP_ID_500931420 m1A Human chr12 + 50764304 50764304 50764304 TTCCCGCCCCGGAGAGCGGCGAGGCGGCAGCCACAGGTAAGTGGGGGGCGGGGAGGGACGTGCCC TTCCCGCCCCGGAGAGCGGCGAGGCGGCAGCCCCAGGTAAGTGGGGGGCGGGGAGGGACGTGCCC A C ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:50764067..50764336;chr12:50764109..50764384 26863196 MeRIP-seq:(Medium) rs1381275533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246654,Human_RBP_ID_8940707 Human_Splice_Rec_1368759,Human_Splice_Rec_1368767 RMVar_hsa_circ_93027,RMVar_hsa_circ_156530 90525 RMVar_ID_90525 Human_SNP_ID_500971235 m1A Human chr12 + 50930419 50930419 50930419 CTTCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCAGCTAATTTGT CTTCTGCCTCAGCCTCCCTAGTAGCTGGGATTGCAGGTGCCCACCACCATGCCCAGCTAATTTGT A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1238121802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368823 90526 RMVar_ID_90526 Human_SNP_ID_500971520 m1A Human chr12 + 50931564 50931564 50931564 CCCTACTAAAGATACAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA CCCTACTAAAGATACAAAAAAAAAAAAAAATTGGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1293174705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26416893 90527 RMVar_ID_90527 Human_SNP_ID_500971521 m1A Human chr12 + 50931564 50931564 50931564 CCCTACTAAAGATACAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA CCCTACTAAAGATACAAAAAAAAAAAAAAATTTGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA A T METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1293174705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26416893 90528 RMVar_ID_90528 Human_SNP_ID_500984280 m1A Human chr12 - 50986482 50986482 50986482 TCAGTCTCAGATTTACAAGCATTTAGGAGCCTAGGTAAAAGCTGCTAGTATTCTTTTAAAAGTTA TCAGTCTCAGATTTACAAGCATTTAGGAGCCTGGGTAAAAGCTGCTAGTATTCTTTTAAAAGTTA T C SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:50986433..50986595 26863196 MeRIP-seq:(Medium) rs1276911768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16423,RMVar_hsa_circ_64705,RMVar_hsa_circ_299421,RMVar_hsa_circ_38990,RMVar_hsa_circ_156541 90529 RMVar_ID_90529 Human_SNP_ID_500999859 m1A Human chr12 - 51048427 51048427 51048427 GGCCAGAGCGACCAAGTTGCAGCCTCCGGGTGACAAAATGTCCAGGGGTGACTGCCGAGCCCCAC GGCCAGAGCGACCAAGTTGCAGCCTCCGGGTGGCAAAATGTCCAGGGGTGACTGCCGAGCCCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51048376..51048442 26863196 MeRIP-seq:(Medium) rs1265693922 Functional Loss SNV dbSNP153 33..33 33 - - - 90530 RMVar_ID_90530 Human_SNP_ID_500999860 m1A Human chr12 - 51048427 51048427 51048427 GGCCAGAGCGACCAAGTTGCAGCCTCCGGGTGACAAAATGTCCAGGGGTGACTGCCGAGCCCCAC GGCCAGAGCGACCAAGTTGCAGCCTCCGGGTGCCAAAATGTCCAGGGGTGACTGCCGAGCCCCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51048376..51048442 26863196 MeRIP-seq:(Medium) rs1265693922 Functional Loss SNV dbSNP153 33..33 33 - - - 90531 RMVar_ID_90531 Human_SNP_ID_501007220 m1A Human chr12 + 51076671 51076671 51076671 ATTAGGATTCTGCCCAGGGAAAAAAAGGAATCAGCATTCCTGTCCCCAGACAGACTCCTCCCCAG ATTAGGATTCTGCCCAGGGAAAAAAAGGAATCCGCATTCCTGTCCCCAGACAGACTCCTCCCCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51076667..51076761 26863196 MeRIP-seq:(Medium) rs1198866541 Functional Loss SNV dbSNP153 33..33 33 - - - 90532 RMVar_ID_90532 Human_SNP_ID_501008967 m1A Human chr12 - 51083535 51083535 51083535 GCGTCTGCTGCCGGGGGCGCCCGAGTTGCCGGAGACGCCCGGCCCTCTCTGCCTGCCGGCTGGGC GCGTCTGCTGCCGGGGGCGCCCGAGTTGCCGGGGACGCCCGGCCCTCTCTGCCTGCCGGCTGGGC T C CSRNP2 Ensembl:ENSG00000110925 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:51082872..51083575 26863196 MeRIP-seq:(Medium) rs1332508121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247451,Human_RBP_ID_9322513,Human_RBP_ID_18417269 90533 RMVar_ID_90533 Human_SNP_ID_501030415 m1A Human chr12 + 51171945 51171945 51171945 CCAGCTCCCAATTTCCCAACTTCCTAGATACCATTCCTATGCTATATGTAACCCTTCTTCACACA CCAGCTCCCAATTTCCCAACTTCCTAGATACCGTTCCTATGCTATATGTAACCCTTCTTCACACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51171923..51172085 26863196 MeRIP-seq:(Medium) rs144568125 Functional Loss SNV dbSNP153 33..33 33 - - - 90534 RMVar_ID_90534 Human_SNP_ID_501030419 m1A Human chr12 - 51171967 51171965 51171968 TATGTGTGGGTAAGTCTGACGTTGTGTGAAGAAGGGTTACATATAGCATAGGAATGGTATCTAGG TATGTGTGGGTAAGTCTGACGTTGTGTGAAG___GGTTACATATAGCATAGGAATGGTATCTAGG CCTT C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51171935..51172022 26863196 MeRIP-seq:(Medium) rs994153356 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2342552,Human_RBP_ID_11970288,Human_RBP_ID_23563742 90535 RMVar_ID_90535 Human_SNP_ID_501036342 m1A Human chr12 + 51195943 51195943 51195943 AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCCACCCCCCACCCCCCCCAGCCCCTGTACCTCACT AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCCCCCCCCCACCCCCCCCAGCCCCTGTACCTCACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:51195942..51196052 26863196 MeRIP-seq:(Medium) rs765266326 Functional Loss SNV dbSNP153 33..33 33 - - - 90536 RMVar_ID_90536 Human_SNP_ID_501047642 m1A Human chr12 + 51238905 51238905 51238905 CCGCGACGCCGAGACAAACCGGACCCGCAACCACCATGAACAGCAAAGGCAAGGACCGAGGGTGG CCGCGACGCCGAGACAAACCGGACCCGCAACCGCCATGAACAGCAAAGGCAAGGACCGAGGGTGG A G DAZAP2 Ensembl:ENSG00000183283 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51238826..51239039 26863196 MeRIP-seq:(Medium) rs1290301130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876557,Human_RBP_ID_4246662,Human_RBP_ID_11970407,Human_RBP_ID_17238982,Human_RBP_ID_17357015 Human_Splice_Rec_1369917 RMVar_hsa_circ_156588,RMVar_hsa_circ_77809 90537 RMVar_ID_90537 Human_SNP_ID_501047645 m1A Human chr12 + 51238919 51238919 51238919 CAAACCGGACCCGCAACCACCATGAACAGCAAAGGCAAGGACCGAGGGTGGCAGAGGCCGTCGGG CAAACCGGACCCGCAACCACCATGAACAGCAAGGGCAAGGACCGAGGGTGGCAGAGGCCGTCGGG A G DAZAP2 Ensembl:ENSG00000183283 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:51238826..51238978;chr12:51238851..51238950 26863410 MeRIP-seq:(Medium) rs1451550764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246662,Human_RBP_ID_17357015,Human_RBP_ID_19056172,Human_RBP_ID_26416974 Human_Splice_Rec_1369909,Human_Splice_Rec_1369917 RMVar_hsa_circ_156588,RMVar_hsa_circ_77809 90538 RMVar_ID_90538 Human_SNP_ID_501048187 m1A Human chr12 - 51240302 51240300 51240302 CAAGAAAAAAATGAAGGTTGCCTACTACACAGAGCTACCAAAATGAGGCAGGTCATATCGGGTAG CAAGAAAAAAATGAAGGTTGCCTACTACACAG__CTACCAAAATGAGGCAGGTCATATCGGGTAG GCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51240298..51240475 26863196 MeRIP-seq:(Medium) rs1366526126 Functional Loss DEL dbSNP153 33..34 33 - - - 90539 RMVar_ID_90539 Human_SNP_ID_501048214 m1A Human chr12 - 51240401 51240401 51240401 TAGGGTGGAGCCTGAGGAAGATGCAAGGTCTGAGGGTATACTGGATTCCCAGGAGGCTGCACAGG TAGGGTGGAGCCTGAGGAAGATGCAAGGTCTGCGGGTATACTGGATTCCCAGGAGGCTGCACAGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:51240351..51240400 26863196 MeRIP-seq:(Medium) rs1170011440 Functional Loss SNV dbSNP153 33..33 33 - - - 90540 RMVar_ID_90540 Human_SNP_ID_501048222 m1A Human chr12 - 51240425 51240425 51240425 GAGTAGGCAGGTGGAGCATCGGTATAGGGTGGAGCCTGAGGAAGATGCAAGGTCTGAGGGTATAC GAGTAGGCAGGTGGAGCATCGGTATAGGGTGGTGCCTGAGGAAGATGCAAGGTCTGAGGGTATAC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:51240376..51240475 26863196 MeRIP-seq:(Medium) rs1383186662 Functional Loss SNV dbSNP153 33..33 33 - - - 90541 RMVar_ID_90541 Human_SNP_ID_501048230 m1A Human chr12 - 51240449 51240449 51240449 ATCTGGCAAACTGGAAGCACCTCTGAGTAGGCAGGTGGAGCATCGGTATAGGGTGGAGCCTGAGG ATCTGGCAAACTGGAAGCACCTCTGAGTAGGCTGGTGGAGCATCGGTATAGGGTGGAGCCTGAGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:51240426..51240450;chr12:51240401..51240475 26863196 MeRIP-seq:(Medium) rs756531434 Functional Loss SNV dbSNP153 33..33 33 - - - 90542 RMVar_ID_90542 Human_SNP_ID_501048320 m1A Human chr12 - 51240854 51240849 51240854 AGCTCGGACGATAGAGCTAGAAGAGGCAGAAGAGAAGGCAAAATGTTACTTTATGACATTCCTAT AGCTCGGACGATAGAGCTAGAAGAGGCAGAAG_____GCAAAATGTTACTTTATGACATTCCTAT CCTTCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51240851..51240950 26863196 MeRIP-seq:(Medium) rs781710160 Functional Loss DEL dbSNP153 33..37 33 - - - 90543 RMVar_ID_90543 Human_SNP_ID_501048351 m1A Human chr12 - 51240920 51240920 51240920 GATACAGAGAGGCTCCAGGAAATGCGGCTGACATGGTGGGGACTGTGGCAGCCCCTGGGTGCACA GATACAGAGAGGCTCCAGGAAATGCGGCTGACGTGGTGGGGACTGTGGCAGCCCCTGGGTGCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51240851..51240975 26863196 MeRIP-seq:(Medium) rs776418321 Functional Loss SNV dbSNP153 33..33 33 - - - 90544 RMVar_ID_90544 Human_SNP_ID_501048383 m1A Human chr12 - 51241023 51241023 51241023 ACCAGCACTGTGGAGCCAGGTGGATAGATGGGACCGACTGGATAATAAGCCATGGGGATTGTGGA ACCAGCACTGTGGAGCCAGGTGGATAGATGGGGCCGACTGGATAATAAGCCATGGGGATTGTGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51240976..51241025 26863196 MeRIP-seq:(Medium) rs746731238 Functional Loss SNV dbSNP153 33..33 33 - - - 90545 RMVar_ID_90545 Human_SNP_ID_501048861 m1A Human chr12 + 51242787 51242787 51242787 GGTCTTTGCTTTTAGTAATAAAACATCAAATTAGGTTTGGAGGGAACTTTGATCTTCCTAAGAAT GGTCTTTGCTTTTAGTAATAAAACATCAAATTGGGTTTGGAGGGAACTTTGATCTTCCTAAGAAT A G DAZAP2 Ensembl:ENSG00000183283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:51242743..51242893 32194978 MeRIP-seq:(Medium) rs552716848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421895,Human_RBP_ID_1796700,Human_RBP_ID_3408007,Human_RBP_ID_4256076,Human_RBP_ID_6194955,Human_RBP_ID_9018096,Human_RBP_ID_11970510,Human_RBP_ID_17238993,Human_RBP_ID_17354761,Human_RBP_ID_17471856,Human_RBP_ID_17821348,Human_RBP_ID_21908502,Human_RBP_ID_23563792,Human_RBP_ID_26416988 90546 RMVar_ID_90546 Human_SNP_ID_501056275 m1A Human chr12 - 51270905 51270905 51270905 TTAATTTGCCCAAAGTCACCCAGCTAGCAAGCAGAAGAGCTGGGGCTGTTTGAATCCAAAGTCCA TTAATTTGCCCAAAGTCACCCAGCTAGCAAGCCGAAGAGCTGGGGCTGTTTGAATCCAAAGTCCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:51270856..51270942 32194978 MeRIP-seq:(Medium) rs1369606782 Functional Loss SNV dbSNP153 33..33 33 - - - 90547 RMVar_ID_90547 Human_SNP_ID_501086430 m1A Human chr12 + 51391361 51391361 51391361 AGCGCCAAGGTGGAGGGGGGTCCTACCGAGGGAGGAGCTACAGGCCACCGCGACCAGCAGAGAGC AGCGCCAAGGTGGAGGGGGGTCCTACCGAGGGGGGAGCTACAGGCCACCGCGACCAGCAGAGAGC A G SLC4A8 Ensembl:ENSG00000050438 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51391357..51391633 26863196 MeRIP-seq:(Medium) rs1565742612 Functional Loss SNV dbSNP153 33..33 33 - - - 90548 RMVar_ID_90548 Human_SNP_ID_501086467 m1A Human chr12 + 51391481 51391478 51391481 GAGGAGGAAGAGGAAGAGGCGAAGGCTGGCGGAGGAGGAGGTGAGAGCGAGGACTCGGCAGAAGC GAGGAGGAAGAGGAAGAGGCGAAGGCTGGC___GGAGGAGGTGAGAGCGAGGACTCGGCAGAAGC CGGA C SLC4A8 Ensembl:ENSG00000050438 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51391480..51391638 26863196 MeRIP-seq:(Medium) rs1375354028 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_1370265,Human_Splice_Rec_1370293,Human_Splice_Rec_1370341 90549 RMVar_ID_90549 Human_SNP_ID_501086469 m1A Human chr12 + 51391481 51391481 51391481 GAGGAGGAAGAGGAAGAGGCGAAGGCTGGCGGAGGAGGAGGTGAGAGCGAGGACTCGGCAGAAGC GAGGAGGAAGAGGAAGAGGCGAAGGCTGGCGGGGGAGGAGGTGAGAGCGAGGACTCGGCAGAAGC A G SLC4A8 Ensembl:ENSG00000050438 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51391480..51391638 26863196 MeRIP-seq:(Medium) rs567261935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1370265,Human_Splice_Rec_1370293,Human_Splice_Rec_1370341 90550 RMVar_ID_90550 Human_SNP_ID_501086589 m1A Human chr12 - 51391825 51391825 51391825 CCGCAAAGACCGCACCCCCGGGGCGGGCTGAGACGCAGAGAAGCCGGGGCGCCCCTCTGCCGGTC CCGCAAAGACCGCACCCCCGGGGCGGGCTGAGGCGCAGAGAAGCCGGGGCGCCCCTCTGCCGGTC T C GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:51391776..51391861 26863410 MeRIP-seq:(Medium) rs1408268625 Functional Loss SNV dbSNP153 33..33 33 - - - 90551 RMVar_ID_90551 Human_SNP_ID_501097774 m1A Human chr12 + 51440647 51440647 51440647 CGTAAGTATCTCAAAAGGATCTGGCATACACAAGGTTTGTATATTTGAACGAGGTATGTGTATTA CGTAAGTATCTCAAAAGGATCTGGCATACACAGGGTTTGTATATTTGAACGAGGTATGTGTATTA A G SLC4A8 Ensembl:ENSG00000050438 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51440640..51440838 26863196 MeRIP-seq:(Medium) rs1164325272 Functional Loss SNV dbSNP153 33..33 33 - - - 90552 RMVar_ID_90552 Human_SNP_ID_501099557 m1A Human chr12 - 51448714 51448712 51448714 TATCATCTTACATCTCTCTCAGCTTAGTTCAAAAGACTTTCTTGAGAGCCCACCACGTTGCAGGC TATCATCTTACATCTCTCTCAGCTTAGTTCAA__GACTTTCTTGAGAGCCCACCACGTTGCAGGC CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51448711..51449085 26863196 MeRIP-seq:(Medium) rs1565783488 Functional Loss DEL dbSNP153 33..34 33 - - - 90553 RMVar_ID_90553 Human_SNP_ID_501099563 m1A Human chr12 - 51448760 51448760 51448760 AAGCTTCCCTCATTAGGGACACCACACCACTCATTCACCAAATCTCTATCATCTTACATCTCTCT AAGCTTCCCTCATTAGGGACACCACACCACTCTTTCACCAAATCTCTATCATCTTACATCTCTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51448756..51449045 26863196 MeRIP-seq:(Medium) rs1043319708 Functional Loss SNV dbSNP153 33..33 33 - - - 90554 RMVar_ID_90554 Human_SNP_ID_501109186 m1A Human chr12 + 51491285 51491285 51491285 AGTCAACAGCACATAGGTGGTATTGAAAGCCGAGGGAATAGATGAGAGAACTCAGGGAAAAGAGA AGTCAACAGCACATAGGTGGTATTGAAAGCCGCGGGAATAGATGAGAGAACTCAGGGAAAAGAGA A C SLC4A8 Ensembl:ENSG00000050438 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51491236..51491319 26863196 MeRIP-seq:(Medium) rs1315042383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16448,RMVar_hsa_circ_48197,RMVar_hsa_circ_265102,RMVar_hsa_circ_30818,RMVar_hsa_circ_319283,RMVar_hsa_circ_156605,RMVar_hsa_circ_156606 90555 RMVar_ID_90555 Human_SNP_ID_501118951 m1A Human chr12 + 51534783 51534783 51534783 GAGGGTAAGGGGACGGAGAATGATGGGGTTATATGTGAGGTGTGTGCCTTTAGCCAGGGTAGGCA GAGGGTAAGGGGACGGAGAATGATGGGGTTATCTGTGAGGTGTGTGCCTTTAGCCAGGGTAGGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:51534734..51534834 26863196 MeRIP-seq:(Medium) rs555413068 Functional Loss SNV dbSNP153 33..33 33 - - - 90556 RMVar_ID_90556 Human_SNP_ID_501118960 m1A Human chr12 + 51534815 51534814 51534815 ATGTGAGGTGTGTGCCTTTAGCCAGGGTAGGCAGGGGAGGCCTTTCGGAAGGGGTGGTGTCTGGG ATGTGAGGTGTGTGCCTTTAGCCAGGGTAGGC_GGGGAGGCCTTTCGGAAGGGGTGGTGTCTGGG CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51534765..51535028 26863196 MeRIP-seq:(Medium) rs1212346040 Functional Loss DEL dbSNP153 33..33 33 - - - 90557 RMVar_ID_90557 Human_SNP_ID_501118961 m1A Human chr12 + 51534815 51534815 51534815 ATGTGAGGTGTGTGCCTTTAGCCAGGGTAGGCAGGGGAGGCCTTTCGGAAGGGGTGGTGTCTGGG ATGTGAGGTGTGTGCCTTTAGCCAGGGTAGGCCGGGGAGGCCTTTCGGAAGGGGTGGTGTCTGGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51534765..51535028 26863196 MeRIP-seq:(Medium) rs1278206770 Functional Loss SNV dbSNP153 33..33 33 - - - 90558 RMVar_ID_90558 Human_SNP_ID_501131684 m1A Human chr12 - 51591339 51591339 51591339 GGGGCGACTTACGGCAGCGGCGGCGGCGAGGGAGGCAGCGGCGGCCCTAACGCGGGGCCCGGGAG GGGGCGACTTACGGCAGCGGCGGCGGCGAGGGGGGCAGCGGCGGCCCTAACGCGGGGCCCGGGAG T C lnc-GALNT6-4,lnc-GALNT6-4:2,lnc-GALNT6-4:3,lnc-GALNT6-4:4 RNACentral:URS0000D5A987,RNACentral:URS0000D58163,RNACentral:URS0000D5AC8E,RNACentral:URS0000D58521 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51591304..51591399 26863196 MeRIP-seq:(Medium) rs966694569 Functional Loss SNV dbSNP153 33..33 33 - - - 90559 RMVar_ID_90559 Human_SNP_ID_501140258 m1A Human chr12 + 51629775 51629775 51629775 TCTCTGTGGCATACTCTTGGGAGAGGGCTAAGAGGTGGGAAGGAGAAGCTGAGATGAGGTTTGAG TCTCTGTGGCATACTCTTGGGAGAGGGCTAAGCGGTGGGAAGGAGAAGCTGAGATGAGGTTTGAG A C SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51629770..51629835 26863196 MeRIP-seq:(Medium) rs559570501 Functional Loss SNV dbSNP153 33..33 33 - - - 90560 RMVar_ID_90560 Human_SNP_ID_501149447 m1A Human chr12 + 51670555 51670555 51670555 AAATCCTGGAGGGCTTAGAATGTTAGACTCAGAGGTGTGGTGTTTGTTTGAGAAGCAGTAGAGAA AAATCCTGGAGGGCTTAGAATGTTAGACTCAGTGGTGTGGTGTTTGTTTGAGAAGCAGTAGAGAA A T SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51670505..51670671 26863196 MeRIP-seq:(Medium) rs1389289256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26994,RMVar_hsa_circ_328375,RMVar_hsa_circ_377737,RMVar_hsa_circ_81553,RMVar_hsa_circ_68047,RMVar_hsa_circ_156610,RMVar_hsa_circ_22444,RMVar_hsa_circ_156611 90561 RMVar_ID_90561 Human_SNP_ID_501157419 m1A Human chr12 + 51706563 51706563 51706563 GCTCAAAGAGTGCAAAGGAAAGACGTAACAGGAGAAAGAAGAGGAAGCAAAAGGAACTCTCTGAA GCTCAAAGAGTGCAAAGGAAAGACGTAACAGGTGAAAGAAGAGGAAGCAAAAGGAACTCTCTGAA A T SCN8A Ensembl:ENSG00000196876 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:51706513..51706673 26863196 MeRIP-seq:(Medium) rs1555219759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377737,RMVar_hsa_circ_334700,RMVar_hsa_circ_6090,RMVar_hsa_circ_156618,RMVar_hsa_circ_71367,RMVar_hsa_circ_329115,RMVar_hsa_circ_329521,RMVar_hsa_circ_376897,RMVar_hsa_circ_290732,RMVar_hsa_circ_41834,RMVar_hsa_circ_91826,RMVar_hsa_circ_34336,RMVar_hsa_circ_156620,RMVar_hsa_circ_156622,RMVar_hsa_circ_156621,RMVar_hsa_circ_156619,RMVar_hsa_circ_268479,RMVar_hsa_circ_104372,RMVar_hsa_circ_156626,RMVar_hsa_circ_5823,RMVar_hsa_circ_156625,RMVar_hsa_circ_302349,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627 90562 RMVar_ID_90562 Human_SNP_ID_501157442 m1A Human chr12 + 51706600 51706600 51706600 GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGAGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGCGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT A C SCN8A Ensembl:ENSG00000196876 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51706550..51706660 26863196 MeRIP-seq:(Medium) rs371383623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377737,RMVar_hsa_circ_334700,RMVar_hsa_circ_6090,RMVar_hsa_circ_156618,RMVar_hsa_circ_71367,RMVar_hsa_circ_329115,RMVar_hsa_circ_329521,RMVar_hsa_circ_376897,RMVar_hsa_circ_290732,RMVar_hsa_circ_41834,RMVar_hsa_circ_91826,RMVar_hsa_circ_34336,RMVar_hsa_circ_156620,RMVar_hsa_circ_156622,RMVar_hsa_circ_156621,RMVar_hsa_circ_156619,RMVar_hsa_circ_268479,RMVar_hsa_circ_104372,RMVar_hsa_circ_156626,RMVar_hsa_circ_5823,RMVar_hsa_circ_156625,RMVar_hsa_circ_302349,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627 90563 RMVar_ID_90563 Human_SNP_ID_501157443 m1A Human chr12 + 51706600 51706600 51706600 GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGAGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGGGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT A G SCN8A Ensembl:ENSG00000196876 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51706550..51706660 26863196 MeRIP-seq:(Medium) rs371383623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377737,RMVar_hsa_circ_334700,RMVar_hsa_circ_6090,RMVar_hsa_circ_156618,RMVar_hsa_circ_71367,RMVar_hsa_circ_329115,RMVar_hsa_circ_329521,RMVar_hsa_circ_376897,RMVar_hsa_circ_290732,RMVar_hsa_circ_41834,RMVar_hsa_circ_91826,RMVar_hsa_circ_34336,RMVar_hsa_circ_156620,RMVar_hsa_circ_156622,RMVar_hsa_circ_156621,RMVar_hsa_circ_156619,RMVar_hsa_circ_268479,RMVar_hsa_circ_104372,RMVar_hsa_circ_156626,RMVar_hsa_circ_5823,RMVar_hsa_circ_156625,RMVar_hsa_circ_302349,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627 90564 RMVar_ID_90564 Human_SNP_ID_501167169 m1A Human chr12 + 51750351 51750351 51750351 ACGGAGAAGATAAGACAAAGGAGAGAAAGAAAAAGGAAAGAAGATGATGACCCAGGGAGGGAAGG ACGGAGAAGATAAGACAAAGGAGAGAAAGAAATAGGAAAGAAGATGATGACCCAGGGAGGGAAGG A T SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51750328..51750522 26863196 MeRIP-seq:(Medium) rs1236593257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13785,RMVar_hsa_circ_6090,RMVar_hsa_circ_329115,RMVar_hsa_circ_329521,RMVar_hsa_circ_91826,RMVar_hsa_circ_34336,RMVar_hsa_circ_156620,RMVar_hsa_circ_156621,RMVar_hsa_circ_156619,RMVar_hsa_circ_268479,RMVar_hsa_circ_104372,RMVar_hsa_circ_156625,RMVar_hsa_circ_156629,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627,RMVar_hsa_circ_357355,RMVar_hsa_circ_355780,RMVar_hsa_circ_272342,RMVar_hsa_circ_336151,RMVar_hsa_circ_341453,RMVar_hsa_circ_309902,RMVar_hsa_circ_38865,RMVar_hsa_circ_156631,RMVar_hsa_circ_156632,RMVar_hsa_circ_156633,RMVar_hsa_circ_156630 90565 RMVar_ID_90565 Human_SNP_ID_501223312 m1A Human chr12 + 51976356 51976356 51976356 CAGGTCACCTCAAGGAGCCTGAGCACCCGTCCATGTGGGGCCCGGTGGAGCTGGTAGGCATCATC CAGGTCACCTCAAGGAGCCTGAGCACCCGTCCCTGTGGGGCCCGGTGGAGCTGGTAGGCATCATC A C ACVR1B Ensembl:ENSG00000135503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:51975293..51976416 32194978 MeRIP-seq:(Medium) rs375985263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421964,Human_RBP_ID_4227513,Human_RBP_ID_6195378,Human_RBP_ID_8782667,Human_RBP_ID_18628471 Human_Splice_Rec_1371228,Human_Splice_Rec_1371244,Human_Splice_Rec_1371262,Human_Splice_Rec_1371278,Human_Splice_Rec_1371282,Human_Splice_Rec_1371294 RMVar_hsa_circ_62069,RMVar_hsa_circ_366366,RMVar_hsa_circ_281232,RMVar_hsa_circ_156645,RMVar_hsa_circ_44071 90566 RMVar_ID_90566 Human_SNP_ID_501223313 m1A Human chr12 + 51976356 51976356 51976356 CAGGTCACCTCAAGGAGCCTGAGCACCCGTCCATGTGGGGCCCGGTGGAGCTGGTAGGCATCATC CAGGTCACCTCAAGGAGCCTGAGCACCCGTCCGTGTGGGGCCCGGTGGAGCTGGTAGGCATCATC A G ACVR1B Ensembl:ENSG00000135503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:51975293..51976416 32194978 MeRIP-seq:(Medium) rs375985263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421964,Human_RBP_ID_4227513,Human_RBP_ID_6195378,Human_RBP_ID_8782667,Human_RBP_ID_18628471 Human_Splice_Rec_1371228,Human_Splice_Rec_1371244,Human_Splice_Rec_1371262,Human_Splice_Rec_1371278,Human_Splice_Rec_1371282,Human_Splice_Rec_1371294 RMVar_hsa_circ_62069,RMVar_hsa_circ_366366,RMVar_hsa_circ_281232,RMVar_hsa_circ_156645,RMVar_hsa_circ_44071 90567 RMVar_ID_90567 Human_SNP_ID_501228092 m1A Human chr12 - 51994832 51994830 51994832 ACCAGGGAAACTAGATGCTGCTCACTACTGAAAAGAGGCACCAGCAAGCACGGACAGCATGACGA ACCAGGGAAACTAGATGCTGCTCACTACTGAA__GAGGCACCAGCAAGCACGGACAGCATGACGA CTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:51994781..51994882 32194978 MeRIP-seq:(Medium) rs1044867006 Functional Loss DEL dbSNP153 33..34 33 - - - 90568 RMVar_ID_90568 Human_SNP_ID_501228093 m1A Human chr12 - 51994832 51994832 51994832 ACCAGGGAAACTAGATGCTGCTCACTACTGAAAAGAGGCACCAGCAAGCACGGACAGCATGACGA ACCAGGGAAACTAGATGCTGCTCACTACTGAAGAGAGGCACCAGCAAGCACGGACAGCATGACGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:51994781..51994882 32194978 MeRIP-seq:(Medium) rs981962803 Functional Loss SNV dbSNP153 33..33 33 - - - 90569 RMVar_ID_90569 Human_SNP_ID_501233425 m1A Human chr12 + 52015293 52015293 52015293 GGGAGGCCGAGCCAAGAGGACCCCAGGAGCCCAGAGCAGCGGGAGAGGGTCCTTCCTAGCCTCGG GGGAGGCCGAGCCAAGAGGACCCCAGGAGCCCGGAGCAGCGGGAGAGGGTCCTTCCTAGCCTCGG A G GRASP Ensembl:ENSG00000161835 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52015288..52015377 26863196 MeRIP-seq:(Medium) rs564637508 Functional Loss SNV dbSNP153 33..33 33 - - - 90570 RMVar_ID_90570 Human_SNP_ID_501238840 m1A Human chr12 - 52037305 52037305 52037305 GGGGTCCCGGGCGCCGCGAGGGGACCCCCGCCAGTTCCGCCGCCGCCGCCACCTCCTCCTCGCGC GGGGTCCCGGGCGCCGCGAGGGGACCCCCGCCTGTTCCGCCGCCGCCGCCACCTCCTCCTCGCGC T A lnc-KRT80-8-001 RNACentral:URS00008B3809 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52037262..52037387 26863196 MeRIP-seq:(Medium) rs1382726288 Functional Loss SNV dbSNP153 33..33 33 - - - 90571 RMVar_ID_90571 Human_SNP_ID_501240054 m1A Human chr12 - 52041899 52041898 52041899 ACCACTCTGGATGGACCAACAGGCCTTGGCCAACCACATTATCCCGTCTGCCTTCAGGGCCCAGC ACCACTCTGGATGGACCAACAGGCCTTGGCCA_CCACATTATCCCGTCTGCCTTCAGGGCCCAGC GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52038538..52043489 32194978 MeRIP-seq:(Medium) rs1446166274 Functional Loss DEL dbSNP153 33..33 33 - - - 90572 RMVar_ID_90572 Human_SNP_ID_501240070 m1A Human chr12 - 52041928 52041928 52041928 GGTGTACAAAGGACAATAGCAGAGCACTTACCACTCTGGATGGACCAACAGGCCTTGGCCAACCA GGTGTACAAAGGACAATAGCAGAGCACTTACCTCTCTGGATGGACCAACAGGCCTTGGCCAACCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52041918..52042344 26863196 MeRIP-seq:(Medium) rs1340648167 Functional Loss SNV dbSNP153 33..33 33 - - - 90573 RMVar_ID_90573 Human_SNP_ID_501240152 m1A Human chr12 + 52042300 52042300 52042300 CTGGGGGCTGGGCTGGGAGCATCATGGGGCAGACGTGGCAGCGGGGAACTGGCCTGTCTCCCAGG CTGGGGGCTGGGCTGGGAGCATCATGGGGCAGCCGTGGCAGCGGGGAACTGGCCTGTCTCCCAGG A C NR4A1 Ensembl:ENSG00000123358 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52041909..52042391 26863196 MeRIP-seq:(Medium) rs1252732352 Functional Loss SNV dbSNP153 33..33 33 - - - 90574 RMVar_ID_90574 Human_SNP_ID_501240998 m1A Human chr12 - 52045787 52045787 52045787 CTTGCCCAAGCCCTACCATGAGCACATGTATCACTACCTCCCCAAAACCAGCCTCCCAGGGACCC CTTGCCCAAGCCCTACCATGAGCACATGTATCTCTACCTCCCCAAAACCAGCCTCCCAGGGACCC T A HSALNG0091142 RNACentral:URS0000EA917A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52045784..52046035 26863196 MeRIP-seq:(Medium) rs532114254 Functional Loss SNV dbSNP153 33..33 33 - - - 90575 RMVar_ID_90575 Human_SNP_ID_501243662 m1A Human chr12 - 52054675 52054675 52054675 TGGAGGACAGGGCCTCATCCACTGGGCCGCTCAGGGGGCCGGGGTAGCAGCCGTACACCTGGAAG TGGAGGACAGGGCCTCATCCACTGGGCCGCTCCGGGGGCCGGGGTAGCAGCCGTACACCTGGAAG T G MF688637 RNACentral:URS0000DE37B8 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:52054651..52054675 26863196 MeRIP-seq:(Medium) rs1482299297 Functional Loss SNV dbSNP153 33..33 33 - - - 90576 RMVar_ID_90576 Human_SNP_ID_501243737 m1A Human chr12 + 52054844 52054844 52054844 TCGCCCAGCCAGACTTACGAAGGCCTGCGGGCATGGACAGAGCAGCTGCCCAAAGCCTCTGGGCC TCGCCCAGCCAGACTTACGAAGGCCTGCGGGCGTGGACAGAGCAGCTGCCCAAAGCCTCTGGGCC A G NR4A1 Ensembl:ENSG00000123358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52054795..52054926 26863196 MeRIP-seq:(Medium) rs1307051935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2896764,Human_miRNA_ID_2907824,Human_miRNA_ID_3026662 RMVar_hsa_circ_79002,RMVar_hsa_circ_76916,RMVar_hsa_circ_156653,RMVar_hsa_circ_82671,RMVar_hsa_circ_156654,RMVar_hsa_circ_156655 90577 RMVar_ID_90577 Human_SNP_ID_501244378 m1A Human chr12 + 52056575 52056575 52056575 ACCCAAGCAGCCCCCAGATGCCTCCCCTGCCAATCTCCTCACTTCCCTGGTCCGTGCACACCTGG ACCCAAGCAGCCCCCAGATGCCTCCCCTGCCAGTCTCCTCACTTCCCTGGTCCGTGCACACCTGG A G NR4A1 Ensembl:ENSG00000123358 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52056526..52056725 26863196 MeRIP-seq:(Medium) rs764214561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27422792 Human_Splice_Rec_1371384,Human_Splice_Rec_1371385,Human_Splice_Rec_1371408,Human_Splice_Rec_1371409,Human_Splice_Rec_1371420,Human_Splice_Rec_1371421,Human_Splice_Rec_1371442,Human_Splice_Rec_1371443,Human_Splice_Rec_1371458,Human_Splice_Rec_1371459,Human_Splice_Rec_1371472,Human_Splice_Rec_1371473,Human_Splice_Rec_1371486,Human_Splice_Rec_1371487,Human_Splice_Rec_1371496,Human_Splice_Rec_1371498,Human_Splice_Rec_1371501 Human_miRNA_ID_2370267,Human_miRNA_ID_2706552 RMVar_hsa_circ_79002,RMVar_hsa_circ_76916,RMVar_hsa_circ_156653,RMVar_hsa_circ_82671,RMVar_hsa_circ_156654,RMVar_hsa_circ_87925,RMVar_hsa_circ_156655,RMVar_hsa_circ_156656 90578 RMVar_ID_90578 Human_SNP_ID_501247992 m1A Human chr12 + 52070036 52070036 52070036 GGTGGTCTGGAGCCTGCCGGGAGAGTGGTGGCATCTGAGAGGCTGGTCGTGGACTGTGGTTGGGG GGTGGTCTGGAGCCTGCCGGGAGAGTGGTGGCTTCTGAGAGGCTGGTCGTGGACTGTGGTTGGGG A T ATG101 Ensembl:ENSG00000123395 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52069973..52070273 26863196 MeRIP-seq:(Medium) rs1371033496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4227676,Human_RBP_ID_8229878,Human_RBP_ID_17669016,Human_RBP_ID_18417273 Human_Splice_Rec_1371521,Human_Splice_Rec_1371529 90579 RMVar_ID_90579 Human_SNP_ID_501248062 m1A Human chr12 + 52070234 52070234 52070234 CCCGAGGAGTCCGTTCCTCCCTGGTTACGTGGACTGTGGAGGTTCGCGCGTAGTGGCGGCGGGGG CCCGAGGAGTCCGTTCCTCCCTGGTTACGTGGCCTGTGGAGGTTCGCGCGTAGTGGCGGCGGGGG A C ATG101 Ensembl:ENSG00000123395 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52070023..52070273 32194978 MeRIP-seq:(Medium) rs1429938911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6195532 Human_Splice_Rec_1371511,Human_Splice_Rec_1371519,Human_Splice_Rec_1371527 90580 RMVar_ID_90580 Human_SNP_ID_501249695 m1A Human chr12 - 52076897 52076897 52076897 GGCCAGGGCTACCACATGCACCTTGACCGTCCACACTTCCCATGGGATGCACTCGTCTGAGAATG GGCCAGGGCTACCACATGCACCTTGACCGTCCGCACTTCCCATGGGATGCACTCGTCTGAGAATG T C AC025259.1 Ensembl:ENSG00000257663 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52076848..52076944 26863196 MeRIP-seq:(Medium) rs147124778 Functional Loss SNV dbSNP153 33..33 33 - - - 90581 RMVar_ID_90581 Human_SNP_ID_501273564 m1A Human chr12 + 52170492 52170492 52170492 TGGGACCAGGGGTCTCCAAGGCCTGGTGCACCAAAGCCCGGTGCTCAGGCTGGGAACAACCCGGC TGGGACCAGGGGTCTCCAAGGCCTGGTGCACCGAAGCCCGGTGCTCAGGCTGGGAACAACCCGGC A G LINC00592 Ensembl:ENSG00000258279 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52170045..52170546 32194978 MeRIP-seq:(Medium) rs1378499962 Functional Loss SNV dbSNP153 33..33 33 - - - 90582 RMVar_ID_90582 Human_SNP_ID_501273627 m1A Human chr12 + 52170696 52170696 52170696 TCCGGAGAAGCTGCTGGGAGCTGGCTGGGGGCAGCCCATCCAGTTCTGACTACTGCCTACTGGGA TCCGGAGAAGCTGCTGGGAGCTGGCTGGGGGCGGCCCATCCAGTTCTGACTACTGCCTACTGGGA A G LINC00592 Ensembl:ENSG00000258279 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52170645..52170946 32194978 MeRIP-seq:(Medium) rs1260544875 Functional Loss SNV dbSNP153 33..33 33 - - - 90583 RMVar_ID_90583 Human_SNP_ID_501274099 m1A Human chr12 - 52172276 52172276 52172276 GCAGGACATGGCGCGGCAGCTGCGCAAGTACCAGGAGCTGATGAACGTCAAGCTGGCCCTGGACA GCAGGACATGGCGCGGCAGCTGCGCAAGTACCGGGAGCTGATGAACGTCAAGCTGGCCCTGGACA T C KRT80 Ensembl:ENSG00000167767 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52172228..52172379 32194978 MeRIP-seq:(Medium) rs1296933681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1371659,Human_Splice_Rec_1371675,Human_Splice_Rec_1371687 RMVar_hsa_circ_120230,RMVar_hsa_circ_156658 90584 RMVar_ID_90584 Human_SNP_ID_501274397 m1A Human chr12 + 52173142 52173142 52173142 GCTGCTCTGGAGGCTGCTCCCATACTCGGCCGAGCGGGCGGCCTGCTCCTCCAGCTGGAGGTACA GCTGCTCTGGAGGCTGCTCCCATACTCGGCCGTGCGGGCGGCCTGCTCCTCCAGCTGGAGGTACA A T LINC00592 Ensembl:ENSG00000258279 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52173097..52180532 32194978 MeRIP-seq:(Medium) rs1360075100 Functional Loss SNV dbSNP153 33..33 33 - - - 90585 RMVar_ID_90585 Human_SNP_ID_501277601 m1A Human chr12 - 52185493 52185493 52185493 GGACTCAGCCATCTTCGACCTCGGGCATCTCTATGAGGAATATCAGGGCCGGCTGCAGGAGGAAC GGACTCAGCCATCTTCGACCTCGGGCATCTCTGTGAGGAATATCAGGGCCGGCTGCAGGAGGAAC T C KRT80 Ensembl:ENSG00000167767 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52185444..52185527 26863196 MeRIP-seq:(Medium) rs144271501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1371648,Human_Splice_Rec_1371664 Human_miRNA_ID_2534640,Human_miRNA_ID_2536372,Human_miRNA_ID_2998996 RMVar_hsa_circ_120230,RMVar_hsa_circ_123863,RMVar_hsa_circ_156658,RMVar_hsa_circ_19693,RMVar_hsa_circ_156659 90586 RMVar_ID_90586 Human_SNP_ID_501277772 m1A Human chr12 - 52186037 52186037 52186037 GGGAGCCTCTGTCATCGAGAGGATGAGCACTTAAGGACAGTACTAACCAGGCCCTACCCTGCTGA GGGAGCCTCTGTCATCGAGAGGATGAGCACTTGAGGACAGTACTAACCAGGCCCTACCCTGCTGA T C KRT80 Ensembl:ENSG00000167767 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52186033..52186239 26863196 MeRIP-seq:(Medium) rs1271791947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120230,RMVar_hsa_circ_123863,RMVar_hsa_circ_156658,RMVar_hsa_circ_156659 90587 RMVar_ID_90587 Human_SNP_ID_501279164 m1A Human chr12 + 52191890 52191890 52191890 GCTGCTGAGGCTGCTGAAGCCAACCACGCAGGAGCGGCAGGCCATGGTGCCCCCGGCCGGAAGCA GCTGCTGAGGCTGCTGAAGCCAACCACGCAGGGGCGGCAGGCCATGGTGCCCCCGGCCGGAAGCA A G LINC00592 Ensembl:ENSG00000258279 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52191842..52191979 26863196 MeRIP-seq:(Medium) rs769678489 Functional Loss SNV dbSNP153 33..33 33 - - - 90588 RMVar_ID_90588 Human_SNP_ID_501289476 m1A Human chr12 + 52233280 52233280 52233280 GTGCGCGCTCCTCCTCGCCCGCCGCTAGGTCCATCCCGGCCCAGCCACCATGTCCATCCACTTCA GTGCGCGCTCCTCCTCGCCCGCCGCTAGGTCCGTCCCGGCCCAGCCACCATGTCCATCCACTTCA A G KRT7 Ensembl:ENSG00000135480 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:52233176..52233400 26863196 MeRIP-seq:(Medium) rs774713119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1371720 RMVar_hsa_circ_82510,RMVar_hsa_circ_156660 90589 RMVar_ID_90589 Human_SNP_ID_501290235 m1A Human chr12 + 52235360 52235360 52235360 GCGGAGCATGCAGGATGTGGTGGAGGACTTCAAGAATAAGTAATGCCCCCTGTGCCACATGCGAA GCGGAGCATGCAGGATGTGGTGGAGGACTTCAGGAATAAGTAATGCCCCCTGTGCCACATGCGAA A G KRT7 Ensembl:ENSG00000135480 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52235156..52235470 26863196 MeRIP-seq:(Medium) rs1188292865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1371723,Human_Splice_Rec_1371739 RMVar_hsa_circ_82510,RMVar_hsa_circ_156661,RMVar_hsa_circ_115454,RMVar_hsa_circ_126393,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662 90590 RMVar_ID_90590 Human_SNP_ID_501290367 m1A Human chr12 + 52235883 52235883 52235883 CTAGGAGAGGACACAGAGCCAACTTGGGAAGCAAAGAAGCAGAGAGGGAAAATGGTCATTGTGAG CTAGGAGAGGACACAGAGCCAACTTGGGAAGCCAAGAAGCAGAGAGGGAAAATGGTCATTGTGAG A C KRT7 Ensembl:ENSG00000135480 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52235880..52235973 26863196 MeRIP-seq:(Medium) rs1300460750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82510,RMVar_hsa_circ_156661,RMVar_hsa_circ_115454,RMVar_hsa_circ_126393,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662 90591 RMVar_ID_90591 Human_SNP_ID_501290788 m1A Human chr12 - 52237542 52237542 52237542 CTCACCTTCTTCAGCACCACAAACTCATTCTCAGCAGCTGTGCGGTGGTTAATTTCATCTTCGTA CTCACCTTCTTCAGCACCACAAACTCATTCTCTGCAGCTGTGCGGTGGTTAATTTCATCTTCGTA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52233151..52237644 26863196 MeRIP-seq:(Medium) rs766393536 Functional Loss SNV dbSNP153 33..33 33 - - - 90592 RMVar_ID_90592 Human_SNP_ID_501290789 m1A Human chr12 - 52237542 52237542 52237542 CTCACCTTCTTCAGCACCACAAACTCATTCTCAGCAGCTGTGCGGTGGTTAATTTCATCTTCGTA CTCACCTTCTTCAGCACCACAAACTCATTCTCGGCAGCTGTGCGGTGGTTAATTTCATCTTCGTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52233151..52237644 26863196 MeRIP-seq:(Medium) rs766393536 Functional Loss SNV dbSNP153 33..33 33 - - - 90593 RMVar_ID_90593 Human_SNP_ID_501290799 m1A Human chr12 - 52237571 52237571 52237571 GACAACCCTCCTCGAGCCTGTCTTTCCCACTCACCTTCTTCAGCACCACAAACTCATTCTCAGCA GACAACCCTCCTCGAGCCTGTCTTTCCCACTCTCCTTCTTCAGCACCACAAACTCATTCTCAGCA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:52237526..52237716 26863196 MeRIP-seq:(Medium) rs746006915 Functional Loss SNV dbSNP153 33..33 33 - - - 90594 RMVar_ID_90594 Human_SNP_ID_501291737 m1A Human chr12 - 52241542 52241542 52241542 CCTTGACCTCAGCGATGATGCCGTCCAGGTCCAGGGAGCGACTGTTGTCCATGGACAGCACCACA CCTTGACCTCAGCGATGATGCCGTCCAGGTCCGGGGAGCGACTGTTGTCCATGGACAGCACCACA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:52241451..52241600 26863196 MeRIP-seq:(Medium) rs1258524037 Functional Loss SNV dbSNP153 33..33 33 - - - 90595 RMVar_ID_90595 Human_SNP_ID_501293525 m1A Human chr12 + 52248771 52248768 52248771 TCGCAGGAGTGCCCGCGACTGAGCCGCCTCCCACCACTCCACTCCTCCAGCCACCACCCACAATC TCGCAGGAGTGCCCGCGACTGAGCCGCCTC___CCACTCCACTCCTCCAGCCACCACCCACAATC CCCA C KRT7 Ensembl:ENSG00000135480 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52248545..52248864 26863196 MeRIP-seq:(Medium) rs1565723834 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_27422836 Human_miRNA_ID_845872 RMVar_hsa_circ_82510,RMVar_hsa_circ_115454,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662,RMVar_hsa_circ_94882,RMVar_hsa_circ_82390,RMVar_hsa_circ_156664,RMVar_hsa_circ_156666,RMVar_hsa_circ_80472,RMVar_hsa_circ_105616,RMVar_hsa_circ_127192,RMVar_hsa_circ_156667,RMVar_hsa_circ_116372,RMVar_hsa_circ_156669,RMVar_hsa_circ_124420,RMVar_hsa_circ_156670,RMVar_hsa_circ_156671,RMVar_hsa_circ_156672 90596 RMVar_ID_90596 Human_SNP_ID_501293527 m1A Human chr12 + 52248771 52248771 52248771 TCGCAGGAGTGCCCGCGACTGAGCCGCCTCCCACCACTCCACTCCTCCAGCCACCACCCACAATC TCGCAGGAGTGCCCGCGACTGAGCCGCCTCCCCCCACTCCACTCCTCCAGCCACCACCCACAATC A C KRT7 Ensembl:ENSG00000135480 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52248545..52248864 26863196 MeRIP-seq:(Medium) rs774790732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27422836 Human_miRNA_ID_845872 RMVar_hsa_circ_82510,RMVar_hsa_circ_115454,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662,RMVar_hsa_circ_94882,RMVar_hsa_circ_82390,RMVar_hsa_circ_156664,RMVar_hsa_circ_156666,RMVar_hsa_circ_80472,RMVar_hsa_circ_105616,RMVar_hsa_circ_127192,RMVar_hsa_circ_156667,RMVar_hsa_circ_116372,RMVar_hsa_circ_156669,RMVar_hsa_circ_124420,RMVar_hsa_circ_156670,RMVar_hsa_circ_156671,RMVar_hsa_circ_156672 90597 RMVar_ID_90597 Human_SNP_ID_501293541 m1A Human chr12 + 52248807 52248807 52248807 CTCCACTCCTCCAGCCACCACCCACAATCACAAGAAGATTCCCACCCCTGCCTCCCATGCCTGGT CTCCACTCCTCCAGCCACCACCCACAATCACAGGAAGATTCCCACCCCTGCCTCCCATGCCTGGT A G KRT7 Ensembl:ENSG00000135480 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52248562..52248925 26863196 MeRIP-seq:(Medium) rs753425932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82510,RMVar_hsa_circ_115454,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662,RMVar_hsa_circ_94882,RMVar_hsa_circ_82390,RMVar_hsa_circ_156664,RMVar_hsa_circ_156666,RMVar_hsa_circ_80472,RMVar_hsa_circ_105616,RMVar_hsa_circ_127192,RMVar_hsa_circ_156667,RMVar_hsa_circ_116372,RMVar_hsa_circ_156669,RMVar_hsa_circ_124420,RMVar_hsa_circ_156670,RMVar_hsa_circ_156671,RMVar_hsa_circ_156672 90598 RMVar_ID_90598 Human_SNP_ID_501304763 m1A Human chr12 + 52293502 52293502 52293502 AGGGGAGTATCTGTGAATTTAGGGTGTGAGAGAGTCCATCTAAGGAAGACGGGCAGAGTCAGAGT AGGGGAGTATCTGTGAATTTAGGGTGTGAGAGGGTCCATCTAAGGAAGACGGGCAGAGTCAGAGT A G KRT86 Ensembl:ENSG00000170442 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52293494..52293585 26863196 MeRIP-seq:(Medium) rs376945975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116858,RMVar_hsa_circ_156673 90599 RMVar_ID_90599 Human_SNP_ID_501305324 m1A Human chr12 - 52296150 52296150 52296150 CTTCTTCTAAGTCACCCTGAGAATAATAGTCTAAGACCAAGTATTTCTTTCTCCCTCTTTTCCTA CTTCTTCTAAGTCACCCTGAGAATAATAGTCTGAGACCAAGTATTTCTTTCTCCCTCTTTTCCTA T C lnc-KRT81-1 RNACentral:URS00008C0941 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:52296100..52296226 26863196 MeRIP-seq:(Medium) rs1253650562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110768,RMVar_hsa_circ_104159,RMVar_hsa_circ_80471,RMVar_hsa_circ_156681,RMVar_hsa_circ_156682,RMVar_hsa_circ_156683 90600 RMVar_ID_90600 Human_SNP_ID_501308933 m1A Human chr12 + 52308719 52308719 52308719 CGCCCGCTGCCTGCACTCTAAGCGCCCTCCCCACCGCTCCGCTCCGGGAGCCATCCCCGGTCGCA CGCCCGCTGCCTGCACTCTAAGCGCCCTCCCCCCCGCTCCGCTCCGGGAGCCATCCCCGGTCGCA A C KRT86 Ensembl:ENSG00000170442 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52308668..52308768 32194978 MeRIP-seq:(Medium) rs1237005825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83787,RMVar_hsa_circ_156685 90601 RMVar_ID_90601 Human_SNP_ID_501469876 m1A Human chr12 - 52897401 52897334 52897402 AAGTGAACAGCTGCGGCAGCCCCTCCCAGCCTACCCCTCCTGCGCTGCCCCAGAGCCTGGGAAGG AAGTGAACAGCTGCGGCAGCCCCTCCCAGCC__________________________________ TCTCCTGTTCCCAGTGCTACCCTGCATAGCGGCCTCCTTCCCAGGCTCTGGGGCAGCGCAGGAGGGGTA T KRT8 Ensembl:ENSG00000170421 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52897255..52897513 26863196 MeRIP-seq:(Medium) rs1565714581 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_754137,Human_RBP_ID_5111452,Human_RBP_ID_17650365,Human_RBP_ID_22435875,Human_RBP_ID_22756760,Human_RBP_ID_26417156 Human_miRNA_ID_463910,Human_miRNA_ID_1559268,Human_miRNA_ID_2153424,Human_miRNA_ID_2801303,Human_miRNA_ID_3009434 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_123935,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_103290,RMVar_hsa_circ_105363,RMVar_hsa_circ_99916,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_156778,RMVar_hsa_circ_96983,RMVar_hsa_circ_156779,RMVar_hsa_circ_156777,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769 90602 RMVar_ID_90602 Human_SNP_ID_501469904 m1A Human chr12 - 52897401 52897392 52897401 AAGTGAACAGCTGCGGCAGCCCCTCCCAGCCTACCCCTCCTGCGCTGCCCCAGAGCCTGGGAAGG AAGTGAACAGCTGCGGCAGCCCCTCCCAGCCT_________GCGCTGCCCCAGAGCCTGGGAAGG CAGGAGGGGT C KRT8 Ensembl:ENSG00000170421 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52897255..52897513 26863196 MeRIP-seq:(Medium) rs1036842953 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_754137,Human_RBP_ID_5111452,Human_RBP_ID_17650365,Human_RBP_ID_22435875,Human_RBP_ID_22756760,Human_RBP_ID_26417156 Human_miRNA_ID_463910,Human_miRNA_ID_1559268,Human_miRNA_ID_2153424,Human_miRNA_ID_2801303,Human_miRNA_ID_3009434 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_123935,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_103290,RMVar_hsa_circ_105363,RMVar_hsa_circ_99916,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_156778,RMVar_hsa_circ_96983,RMVar_hsa_circ_156779,RMVar_hsa_circ_156777,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769 90603 RMVar_ID_90603 Human_SNP_ID_501469906 m1A Human chr12 + 52897393 52897393 52897393 AGCGGCCTCCTTCCCAGGCTCTGGGGCAGCGCAGGAGGGGTAGGCTGGGAGGGGCTGCCGCAGCT AGCGGCCTCCTTCCCAGGCTCTGGGGCAGCGCTGGAGGGGTAGGCTGGGAGGGGCTGCCGCAGCT A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:52897266..52897608 26863196 MeRIP-seq:(Medium) rs1335514586 Functional Loss SNV dbSNP153 33..33 33 - - - 90604 RMVar_ID_90604 Human_SNP_ID_501469933 m1A Human chr12 + 52897441 52897441 52897441 GAGGGGCTGCCGCAGCTGTTCACTTGGGCAGGACGTCAGAGGACTCAGACACCAGCTTCCCATCA GAGGGGCTGCCGCAGCTGTTCACTTGGGCAGGGCGTCAGAGGACTCAGACACCAGCTTCCCATCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:52897335..52897590;chr12:52897320..52897576 26863196 MeRIP-seq:(Medium) rs1034015084 Functional Loss SNV dbSNP153 33..33 33 - - - 90605 RMVar_ID_90605 Human_SNP_ID_501469937 m1A Human chr12 + 52897448 52897448 52897448 TGCCGCAGCTGTTCACTTGGGCAGGACGTCAGAGGACTCAGACACCAGCTTCCCATCACGTGTCT TGCCGCAGCTGTTCACTTGGGCAGGACGTCAGCGGACTCAGACACCAGCTTCCCATCACGTGTCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52897236..52898577 32194978 MeRIP-seq:(Medium) rs769477619 Functional Loss SNV dbSNP153 33..33 33 - - - 90606 RMVar_ID_90606 Human_SNP_ID_501470374 m1A Human chr12 - 52898787 52898787 52898787 CGAGCTGGAGGCCGCCCTGCAGCGGGCCAAGCAGGACATGGCGCGGCAGCTGCGTGAGTACCAGG CGAGCTGGAGGCCGCCCTGCAGCGGGCCAAGCGGGACATGGCGCGGCAGCTGCGTGAGTACCAGG T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52898676..52898800 32194978 MeRIP-seq:(Medium) rs1229512167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877358,Human_RBP_ID_5111454,Human_RBP_ID_9279624,Human_RBP_ID_9364929,Human_RBP_ID_17650660,Human_RBP_ID_17830805,Human_RBP_ID_18189136,Human_RBP_ID_18469317,Human_RBP_ID_22435878,Human_RBP_ID_22756767,Human_RBP_ID_27154839 Human_miRNA_ID_631587,Human_miRNA_ID_2241605 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_103290,RMVar_hsa_circ_105363,RMVar_hsa_circ_107275,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_96983,RMVar_hsa_circ_156777,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_125884,RMVar_hsa_circ_156769,RMVar_hsa_circ_117415,RMVar_hsa_circ_156781,RMVar_hsa_circ_156782,RMVar_hsa_circ_156780 90607 RMVar_ID_90607 Human_SNP_ID_501470684 m1A Human chr12 + 52899841 52899841 52899841 CGGCTGATGTTCCGGTTCATCTCAGAGATCTCAGTCTTTGTGCGCCGCAGGTCATCCCCGTGCTT CGGCTGATGTTCCGGTTCATCTCAGAGATCTCGGTCTTTGTGCGCCGCAGGTCATCCCCGTGCTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52899788..52900000 26863196 MeRIP-seq:(Medium) rs1342059036 Functional Loss SNV dbSNP153 33..33 33 - - - 90608 RMVar_ID_90608 Human_SNP_ID_501470685 m1A Human chr12 - 52899843 52899843 52899843 GGAAGCACGGGGATGACCTGCGGCGCACAAAGACTGAGATCTCTGAGATGAACCGGAACATCAGC GGAAGCACGGGGATGACCTGCGGCGCACAAAGTCTGAGATCTCTGAGATGAACCGGAACATCAGC T A KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52899793..52899981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_8378444,Human_RBP_ID_18189137,Human_RBP_ID_18434340,Human_RBP_ID_22437062,Human_RBP_ID_27422841 Human_Splice_Rec_1372619,Human_Splice_Rec_1372635,Human_Splice_Rec_1372645,Human_Splice_Rec_1372657,Human_Splice_Rec_1372673,Human_Splice_Rec_1372689,Human_Splice_Rec_1372701 Human_miRNA_ID_3002690 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_105363,RMVar_hsa_circ_107275,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_96983,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_125884,RMVar_hsa_circ_156769,RMVar_hsa_circ_117415,RMVar_hsa_circ_156781,RMVar_hsa_circ_156782,RMVar_hsa_circ_156780 90609 RMVar_ID_90609 Human_SNP_ID_501470686 m1A Human chr12 - 52899843 52899843 52899843 GGAAGCACGGGGATGACCTGCGGCGCACAAAGACTGAGATCTCTGAGATGAACCGGAACATCAGC GGAAGCACGGGGATGACCTGCGGCGCACAAAGGCTGAGATCTCTGAGATGAACCGGAACATCAGC T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52899793..52899981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_8378444,Human_RBP_ID_18189137,Human_RBP_ID_18434340,Human_RBP_ID_22437062,Human_RBP_ID_27422841 Human_Splice_Rec_1372619,Human_Splice_Rec_1372635,Human_Splice_Rec_1372645,Human_Splice_Rec_1372657,Human_Splice_Rec_1372673,Human_Splice_Rec_1372689,Human_Splice_Rec_1372701 Human_miRNA_ID_3002690 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_105363,RMVar_hsa_circ_107275,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_96983,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_125884,RMVar_hsa_circ_156769,RMVar_hsa_circ_117415,RMVar_hsa_circ_156781,RMVar_hsa_circ_156782,RMVar_hsa_circ_156780 90610 RMVar_ID_90610 Human_SNP_ID_501471234 m1A Human chr12 + 52901854 52901854 52901854 AGCACGGTGACTTCAGTTGGGTGGAGGGTGGGAGTTGCTCACTTGTTCTTGAAGTCCTCCACCAG AGCACGGTGACTTCAGTTGGGTGGAGGGTGGGGGTTGCTCACTTGTTCTTGAAGTCCTCCACCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52901851..52901875 26863196 MeRIP-seq:(Medium) rs1387450273 Functional Loss SNV dbSNP153 33..33 33 - - - 90611 RMVar_ID_90611 Human_SNP_ID_501471289 m1A Human chr12 - 52901998 52901998 52901998 TGGAGCCTCCTGCAGCAGCAGAAGACGGCTCGAAGCAACATGGACAACATGTTCGAGAGCTACAT TGGAGCCTCCTGCAGCAGCAGAAGACGGCTCGGAGCAACATGGACAACATGTTCGAGAGCTACAT T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52901945..52902037 26863196 MeRIP-seq:(Medium) rs1555186665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378446,Human_RBP_ID_9344263,Human_RBP_ID_9364938,Human_RBP_ID_18469319,Human_RBP_ID_22437068,Human_RBP_ID_22493407,Human_RBP_ID_22756770 Human_Splice_Rec_1372612,Human_Splice_Rec_1372628,Human_Splice_Rec_1372642,Human_Splice_Rec_1372652,Human_Splice_Rec_1372666,Human_Splice_Rec_1372682,Human_Splice_Rec_1372714,Human_Splice_Rec_1372730,Human_Splice_Rec_1372738 RMVar_hsa_circ_98349,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769,RMVar_hsa_circ_109596,RMVar_hsa_circ_156783 90612 RMVar_ID_90612 Human_SNP_ID_501472132 m1A Human chr12 + 52904767 52904762 52904768 TGGGGTCCACCTCCAGGACAAGGGGGCTCAGCAGGCTCTGGTTGACCGTAACTGCGGTGATGCCT TGGGGTCCACCTCCAGGACAAGGGGGCT______GCTCTGGTTGACCGTAACTGCGGTGATGCCT TCAGCAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52904717..52905075 26863196 MeRIP-seq:(Medium) rs1565719610 Functional Loss DEL dbSNP153 29..34 33 - - - 90613 RMVar_ID_90613 Human_SNP_ID_501472197 m1A Human chr12 + 52904891 52904891 52904891 CACTCGGGAGAAGCTCGAGGAGCTGATGCGGGAACCGGGCCCACTCGTGTAGGAGCGGCTGCTGA CACTCGGGAGAAGCTCGAGGAGCTGATGCGGGCACCGGGCCCACTCGTGTAGGAGCGGCTGCTGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52904705..52905075 26863196 MeRIP-seq:(Medium) rs771489011 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 90614 RMVar_ID_90614 Human_SNP_ID_501472265 m1A Human chr12 - 52905029 52905029 52905029 CCTCACCAAGAAGCAGCTTCTCCGCTCCTTCTAGGATCTCCGCCTGGTTCGGCCCGCCTGCCTCC CCTCACCAAGAAGCAGCTTCTCCGCTCCTTCTGGGATCTCCGCCTGGTTCGGCCCGCCTGCCTCC T C KRT8 Ensembl:ENSG00000170421 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52905026..52905075 26863196 MeRIP-seq:(Medium) rs1312169068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4227790 Human_Splice_Rec_1372626 RMVar_hsa_circ_98349,RMVar_hsa_circ_114394,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769,RMVar_hsa_circ_109596,RMVar_hsa_circ_156783 90615 RMVar_ID_90615 Human_SNP_ID_501482276 m1A Human chr12 + 52943214 52943214 52943214 GCCTCCCGATTTCTCCTGTCCGTCGCTGATAAACTGCTTGAAAGAAAAGTCTACATTTTGCCTCC GCCTCCCGATTTCTCCTGTCCGTCGCTGATAACCTGCTTGAAAGAAAAGTCTACATTTTGCCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52943203..52943464 26863196 MeRIP-seq:(Medium) rs1484206451 Functional Loss SNV dbSNP153 33..33 33 - - - 90616 RMVar_ID_90616 Human_SNP_ID_501483667 m1A Human chr12 - 52949175 52949170 52949176 TGGTGGAGAAGGTGGAGCGAGTGGTGAAGCTCATGCTGTCCGGGGAGAGAGAAAGGACAGGACTC TGGTGGAGAAGGTGGAGCGAGTGGTGAAGCT______GTCCGGGGAGAGAGAAAGGACAGGACTC CAGCATG C KRT8 Ensembl:ENSG00000170421 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr12:52949126..52949325;chr12:52949151..52949175 26863196 MeRIP-seq:(Medium) rs754487715 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_5347327,Human_RBP_ID_19060200,Human_RBP_ID_22538647 RMVar_hsa_circ_98349,RMVar_hsa_circ_156769 90617 RMVar_ID_90617 Human_SNP_ID_501483864 m1A Human chr12 + 52949484 52949484 52949484 TTACCTGGACAGAGTGAGGAGCCTGGAGACCGAGAACCGGAGGCTGGAGAGCAAAATCCGGGAGC TTACCTGGACAGAGTGAGGAGCCTGGAGACCGGGAACCGGAGGCTGGAGAGCAAAATCCGGGAGC A G KRT18 Ensembl:ENSG00000111057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52948768..52949500 32194978 MeRIP-seq:(Medium) rs1218968384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753254,Human_RBP_ID_9279625,Human_RBP_ID_22437074 Human_miRNA_ID_2974040,Human_miRNA_ID_2974041,Human_miRNA_ID_3002691,Human_miRNA_ID_3002692,Human_miRNA_ID_3007228,Human_miRNA_ID_3007229 RMVar_hsa_circ_77044,RMVar_hsa_circ_81084,RMVar_hsa_circ_97258,RMVar_hsa_circ_156785,RMVar_hsa_circ_156786,RMVar_hsa_circ_156787 90618 RMVar_ID_90618 Human_SNP_ID_501484133 m1A Human chr12 - 52950288 52950288 52950288 GATTGTAGAGAGAGGTTGTTCCATGAATAGAAAGCCAGGGATGGGTGGGGTGAGTGTGTAAAAAG GATTGTAGAGAGAGGTTGTTCCATGAATAGAACGCCAGGGATGGGTGGGGTGAGTGTGTAAAAAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52950284..52950408 26863196 MeRIP-seq:(Medium) rs767016965 Functional Loss SNV dbSNP153 33..33 33 - - - 90619 RMVar_ID_90619 Human_SNP_ID_501484159 m1A Human chr12 + 52950347 52950347 52950347 ACAATCCCTCCAGATCTTCGCAAATACTGTGGACAATGCCCGCATCGTTCTGCAGATTGACAATG ACAATCCCTCCAGATCTTCGCAAATACTGTGGGCAATGCCCGCATCGTTCTGCAGATTGACAATG A G KRT18 Ensembl:ENSG00000111057 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:52950326..52950425 32194978 MeRIP-seq:(Medium) rs768434116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753256,Human_RBP_ID_810406,Human_RBP_ID_8786708,Human_RBP_ID_18469321,Human_RBP_ID_22436451,Human_RBP_ID_23113368 Human_Splice_Rec_1372762,Human_Splice_Rec_1372763,Human_Splice_Rec_1372774,Human_Splice_Rec_1372775,Human_Splice_Rec_1372782,Human_Splice_Rec_1372783,Human_Splice_Rec_1372792,Human_Splice_Rec_1372797 RMVar_hsa_circ_78317,RMVar_hsa_circ_77044,RMVar_hsa_circ_81084,RMVar_hsa_circ_97258,RMVar_hsa_circ_156785,RMVar_hsa_circ_156786,RMVar_hsa_circ_113882,RMVar_hsa_circ_156787,RMVar_hsa_circ_156788,RMVar_hsa_circ_156789 90620 RMVar_ID_90620 Human_SNP_ID_501484160 m1A Human chr12 + 52950347 52950347 52950347 ACAATCCCTCCAGATCTTCGCAAATACTGTGGACAATGCCCGCATCGTTCTGCAGATTGACAATG ACAATCCCTCCAGATCTTCGCAAATACTGTGGTCAATGCCCGCATCGTTCTGCAGATTGACAATG A T KRT18 Ensembl:ENSG00000111057 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:52950326..52950425 32194978 MeRIP-seq:(Medium) rs768434116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753256,Human_RBP_ID_810406,Human_RBP_ID_8786708,Human_RBP_ID_18469321,Human_RBP_ID_22436451,Human_RBP_ID_23113368 Human_Splice_Rec_1372762,Human_Splice_Rec_1372763,Human_Splice_Rec_1372774,Human_Splice_Rec_1372775,Human_Splice_Rec_1372782,Human_Splice_Rec_1372783,Human_Splice_Rec_1372792,Human_Splice_Rec_1372797 RMVar_hsa_circ_78317,RMVar_hsa_circ_77044,RMVar_hsa_circ_81084,RMVar_hsa_circ_97258,RMVar_hsa_circ_156785,RMVar_hsa_circ_156786,RMVar_hsa_circ_113882,RMVar_hsa_circ_156787,RMVar_hsa_circ_156788,RMVar_hsa_circ_156789 90621 RMVar_ID_90621 Human_SNP_ID_501487962 m1A Human chr12 - 52964268 52964268 52964268 GCGAGACTCTGTCTCAAACAAACAAACAAAAAACAACCACTTACCACATGGCCCAGCATCTCACT GCGAGACTCTGTCTCAAACAAACAAACAAAAAGCAACCACTTACCACATGGCCCAGCATCTCACT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52964251..52964378 26863196 MeRIP-seq:(Medium) rs1320149106 Functional Loss SNV dbSNP153 33..33 33 - - - 90622 RMVar_ID_90622 Human_SNP_ID_501487963 m1A Human chr12 - 52964268 52964268 52964268 GCGAGACTCTGTCTCAAACAAACAAACAAAAAACAACCACTTACCACATGGCCCAGCATCTCACT GCGAGACTCTGTCTCAAACAAACAAACAAAAACCAACCACTTACCACATGGCCCAGCATCTCACT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52964251..52964378 26863196 MeRIP-seq:(Medium) rs1320149106 Functional Loss SNV dbSNP153 33..33 33 - - - 90623 RMVar_ID_90623 Human_SNP_ID_501499565 m1A Human chr12 - 53006797 53006776 53006797 CACGGTGATTCACGTCTACGAAAAGGCCTCGCACCACCCGCACACCTTTCTGCGCCTCCTTCCCC CACGGTGATTCACGTCTACGAAAAGGCCTCGC_____________________GCCTCCTTCCCC CGCAGAAAGGTGTGCGGGTGGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53006748..53007077 26863196 MeRIP-seq:(Medium) rs1244992118 Functional Loss DEL dbSNP153 33..53 33 - - - 90624 RMVar_ID_90624 Human_SNP_ID_501499677 m1A Human chr12 - 53007042 53007026 53007043 CTAGCGCACGCATTGAAGGCGCGCCCGTCTCTACTACCCTCGTGTCTCCTACCGCGCACGCGCAC CTAGCGCACGCATTGAAGGCGCGCCCGTCTC_________________CTACCGCGCACGCGCAC GGAGACACGAGGGTAGTA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53006791..53007067 26863196 MeRIP-seq:(Medium) rs1315542235 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_5461889,Human_RBP_ID_18206360,Human_RBP_ID_26748051 90625 RMVar_ID_90625 Human_SNP_ID_501502875 m1A Human chr12 + 53018754 53018752 53018754 AACATGGGTCCTCTTGTTCTATGACAGTAGTGAGAGAAGTTTCTTCTAATTTCTTACATTCATTC AACATGGGTCCTCTTGTTCTATGACAGTAGT__GAGAAGTTTCTTCTAATTTCTTACATTCATTC TGA T EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53018751..53018861 26863196 MeRIP-seq:(Medium) rs1304859343 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_40334,RMVar_hsa_circ_76754,RMVar_hsa_circ_156797,RMVar_hsa_circ_86249,RMVar_hsa_circ_123410,RMVar_hsa_circ_294205,RMVar_hsa_circ_304371,RMVar_hsa_circ_348127,RMVar_hsa_circ_301953,RMVar_hsa_circ_283091,RMVar_hsa_circ_95415,RMVar_hsa_circ_116093,RMVar_hsa_circ_156799,RMVar_hsa_circ_156803,RMVar_hsa_circ_156805,RMVar_hsa_circ_156806,RMVar_hsa_circ_156804,RMVar_hsa_circ_156801,RMVar_hsa_circ_156802,RMVar_hsa_circ_156800,RMVar_hsa_circ_156798 90626 RMVar_ID_90626 Human_SNP_ID_501505407 m1A Human chr12 + 53027824 53027824 53027824 TCGTTATGATTCAGACCGGTATCGGGATGGGTATCGGGATGGGTATCGGGATGGCCCACGCCGGG TCGTTATGATTCAGACCGGTATCGGGATGGGTGTCGGGATGGGTATCGGGATGGCCCACGCCGGG A G EIF4B Ensembl:ENSG00000063046 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:53027801..53027875 26863196 MeRIP-seq:(Medium) rs370947800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113121,Human_RBP_ID_228449,Human_RBP_ID_422066,Human_RBP_ID_752887,Human_RBP_ID_809544,Human_RBP_ID_3408186,Human_RBP_ID_9352752,Human_RBP_ID_17821531 Human_Splice_Rec_1372814,Human_Splice_Rec_1372815,Human_Splice_Rec_1372852,Human_Splice_Rec_1372882,Human_Splice_Rec_1372883,Human_Splice_Rec_1372908,Human_Splice_Rec_1372909,Human_Splice_Rec_1372938,Human_Splice_Rec_1372939,Human_Splice_Rec_1372956,Human_Splice_Rec_1372957,Human_Splice_Rec_1372988 RMVar_hsa_circ_76754,RMVar_hsa_circ_156797,RMVar_hsa_circ_82258,RMVar_hsa_circ_86249,RMVar_hsa_circ_123410,RMVar_hsa_circ_348127,RMVar_hsa_circ_283091,RMVar_hsa_circ_95415,RMVar_hsa_circ_116093,RMVar_hsa_circ_156799,RMVar_hsa_circ_156803,RMVar_hsa_circ_156801,RMVar_hsa_circ_156802,RMVar_hsa_circ_156800,RMVar_hsa_circ_334239,RMVar_hsa_circ_156798,RMVar_hsa_circ_371787,RMVar_hsa_circ_101989,RMVar_hsa_circ_91253,RMVar_hsa_circ_156808,RMVar_hsa_circ_156812,RMVar_hsa_circ_156810,RMVar_hsa_circ_156811,RMVar_hsa_circ_156809,RMVar_hsa_circ_13960,RMVar_hsa_circ_322144,RMVar_hsa_circ_109462,RMVar_hsa_circ_156817,RMVar_hsa_circ_156818,RMVar_hsa_circ_284853,RMVar_hsa_circ_304811,RMVar_hsa_circ_371741,RMVar_hsa_circ_104894,RMVar_hsa_circ_99517,RMVar_hsa_circ_156820,RMVar_hsa_circ_156822,RMVar_hsa_circ_156821,RMVar_hsa_circ_156819,RMVar_hsa_circ_307336,RMVar_hsa_circ_156825,RMVar_hsa_circ_89981,RMVar_hsa_circ_310447,RMVar_hsa_circ_353502,RMVar_hsa_circ_368983,RMVar_hsa_circ_115538,RMVar_hsa_circ_271490,RMVar_hsa_circ_112570,RMVar_hsa_circ_156827,RMVar_hsa_circ_156831,RMVar_hsa_circ_93379,RMVar_hsa_circ_95653,RMVar_hsa_circ_156833,RMVar_hsa_circ_156834,RMVar_hsa_circ_156832,RMVar_hsa_circ_156829,RMVar_hsa_circ_156830,RMVar_hsa_circ_156828,RMVar_hsa_circ_156826 90627 RMVar_ID_90627 Human_SNP_ID_501507410 m1A Human chr12 - 53034684 53034684 53034684 GACTTACTTCTGCTAGATGTGGTGGAGGTCCCAGTTTGTGATGACTCACTTCCTGTCCTCGACCG GACTTACTTCTGCTAGATGTGGTGGAGGTCCCGGTTTGTGATGACTCACTTCCTGTCCTCGACCG T C AC068888.1 Ensembl:ENSG00000257337 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53034626..53034762 26863196 MeRIP-seq:(Medium) rs772671728 Functional Loss SNV dbSNP153 33..33 33 - - - 90628 RMVar_ID_90628 Human_SNP_ID_501507414 m1A Human chr12 + 53034699 53034699 53034699 AGTGAGTCATCACAAACTGGGACCTCCACCACATCTAGCAGAAGTAAGTCAGACCAGGGTGGGTA AGTGAGTCATCACAAACTGGGACCTCCACCACGTCTAGCAGAAGTAAGTCAGACCAGGGTGGGTA A G EIF4B Ensembl:ENSG00000063046 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:53034601..53034725 26863196 MeRIP-seq:(Medium) rs1303988905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33257,Human_RBP_ID_422069,Human_RBP_ID_877174,Human_RBP_ID_1473273,Human_RBP_ID_1796778,Human_RBP_ID_5170967,Human_RBP_ID_6195834,Human_RBP_ID_8782690,Human_RBP_ID_17239025,Human_RBP_ID_17684693,Human_RBP_ID_17821536,Human_RBP_ID_18434343,Human_RBP_ID_26805665,Human_RBP_ID_27422861 Human_Splice_Rec_1372820,Human_Splice_Rec_1372821,Human_Splice_Rec_1372888,Human_Splice_Rec_1372889,Human_Splice_Rec_1372914,Human_Splice_Rec_1372915,Human_Splice_Rec_1372944,Human_Splice_Rec_1372945,Human_Splice_Rec_1372962,Human_Splice_Rec_1372993 RMVar_hsa_circ_86249,RMVar_hsa_circ_123410,RMVar_hsa_circ_348127,RMVar_hsa_circ_95415,RMVar_hsa_circ_116093,RMVar_hsa_circ_156799,RMVar_hsa_circ_156801,RMVar_hsa_circ_156802,RMVar_hsa_circ_156800,RMVar_hsa_circ_156798,RMVar_hsa_circ_371787,RMVar_hsa_circ_101989,RMVar_hsa_circ_91253,RMVar_hsa_circ_156808,RMVar_hsa_circ_156810,RMVar_hsa_circ_156809,RMVar_hsa_circ_13960,RMVar_hsa_circ_109462,RMVar_hsa_circ_156818,RMVar_hsa_circ_304811,RMVar_hsa_circ_371741,RMVar_hsa_circ_99517,RMVar_hsa_circ_156820,RMVar_hsa_circ_156819,RMVar_hsa_circ_307336,RMVar_hsa_circ_353502,RMVar_hsa_circ_368983,RMVar_hsa_circ_115538,RMVar_hsa_circ_156831,RMVar_hsa_circ_93379,RMVar_hsa_circ_156833,RMVar_hsa_circ_156834,RMVar_hsa_circ_156832,RMVar_hsa_circ_156829,RMVar_hsa_circ_156830,RMVar_hsa_circ_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_118281,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_19099,RMVar_hsa_circ_296341,RMVar_hsa_circ_351439,RMVar_hsa_circ_156838,RMVar_hsa_circ_156839 90629 RMVar_ID_90629 Human_SNP_ID_501507418 m1A Human chr12 + 53034709 53034709 53034709 CACAAACTGGGACCTCCACCACATCTAGCAGAAGTAAGTCAGACCAGGGTGGGTATCGTGTTATT CACAAACTGGGACCTCCACCACATCTAGCAGACGTAAGTCAGACCAGGGTGGGTATCGTGTTATT A C EIF4B Ensembl:ENSG00000063046 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53034689..53034774 26863196 MeRIP-seq:(Medium) rs759282026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1796778,Human_RBP_ID_2342978,Human_RBP_ID_18434343,Human_RBP_ID_19056206,Human_RBP_ID_26806699 Human_Splice_Rec_1372820,Human_Splice_Rec_1372821,Human_Splice_Rec_1372888,Human_Splice_Rec_1372889,Human_Splice_Rec_1372914,Human_Splice_Rec_1372915,Human_Splice_Rec_1372944,Human_Splice_Rec_1372945,Human_Splice_Rec_1372962,Human_Splice_Rec_1372993 RMVar_hsa_circ_86249,RMVar_hsa_circ_123410,RMVar_hsa_circ_348127,RMVar_hsa_circ_95415,RMVar_hsa_circ_116093,RMVar_hsa_circ_156799,RMVar_hsa_circ_156801,RMVar_hsa_circ_156802,RMVar_hsa_circ_156800,RMVar_hsa_circ_156798,RMVar_hsa_circ_371787,RMVar_hsa_circ_101989,RMVar_hsa_circ_91253,RMVar_hsa_circ_156808,RMVar_hsa_circ_156810,RMVar_hsa_circ_156809,RMVar_hsa_circ_13960,RMVar_hsa_circ_109462,RMVar_hsa_circ_156818,RMVar_hsa_circ_304811,RMVar_hsa_circ_371741,RMVar_hsa_circ_99517,RMVar_hsa_circ_156820,RMVar_hsa_circ_156819,RMVar_hsa_circ_307336,RMVar_hsa_circ_353502,RMVar_hsa_circ_368983,RMVar_hsa_circ_115538,RMVar_hsa_circ_156831,RMVar_hsa_circ_93379,RMVar_hsa_circ_156833,RMVar_hsa_circ_156834,RMVar_hsa_circ_156832,RMVar_hsa_circ_156829,RMVar_hsa_circ_156830,RMVar_hsa_circ_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_118281,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_19099,RMVar_hsa_circ_296341,RMVar_hsa_circ_351439,RMVar_hsa_circ_156838,RMVar_hsa_circ_156839 90630 RMVar_ID_90630 Human_SNP_ID_501508251 m1A Human chr12 - 53037612 53037612 53037612 TACTGTTTCCAAACTGACTCACCTTGTAGGGGACTGCTGCTCTGTGTCTGAGCTCTGAGATCGAG TACTGTTTCCAAACTGACTCACCTTGTAGGGGTCTGCTGCTCTGTGTCTGAGCTCTGAGATCGAG T A AC068888.1 Ensembl:ENSG00000257337 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53037551..53037625 32194978 MeRIP-seq:(Medium) rs760298424 Functional Loss SNV dbSNP153 33..33 33 - - - 90631 RMVar_ID_90631 Human_SNP_ID_501510342 m1A Human chr12 - 53045374 53045374 53045374 GAATGAGTAGGGAGGCACTGGGAGGAGGGGAGAGGCAAGAGTTAGGGGAATACCGAGGAAAGTGG GAATGAGTAGGGAGGCACTGGGAGGAGGGGAGGGGCAAGAGTTAGGGGAATACCGAGGAAAGTGG T C AC068888.1 Ensembl:ENSG00000257337 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53045249..53047183 26863196 MeRIP-seq:(Medium) rs959658535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5645289,Human_RBP_ID_8177382,Human_RBP_ID_9416439 90632 RMVar_ID_90632 Human_SNP_ID_501510507 m1A Human chr12 + 53046051 53046051 53046051 CCCATTAGCTCCATTCCATGAAGTTCCTATCCAGTACCAGGCACTGCAAAAGAAGGGAATGAGGT CCCATTAGCTCCATTCCATGAAGTTCCTATCCGGTACCAGGCACTGCAAAAGAAGGGAATGAGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53046015..53046098 26863196 MeRIP-seq:(Medium) rs966707765 Functional Loss SNV dbSNP153 33..33 33 - - - 90633 RMVar_ID_90633 Human_SNP_ID_501511364 m1A Human chr12 + 53049234 53049234 53049234 TGGGACAGCTGCTGAGGAAGGAGAGCAGACCCAGGAGAGCCATGAAGGTAGTACTCAGGCTTCGG TGGGACAGCTGCTGAGGAAGGAGAGCAGACCCGGGAGAGCCATGAAGGTAGTACTCAGGCTTCGG A G TNS2 Ensembl:ENSG00000111077 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53049218..53049307 26863196 MeRIP-seq:(Medium) rs1330733856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1373185,Human_Splice_Rec_1373241,Human_Splice_Rec_1373257 90634 RMVar_ID_90634 Human_SNP_ID_501512101 m1A Human chr12 + 53052132 53052132 53052132 CTGCCTCCCCCTTCAGATGGCCCTGGCTCCCCATGACAGACACCTCCCATAACCCAGGAGAGCCA CTGCCTCCCCCTTCAGATGGCCCTGGCTCCCCGTGACAGACACCTCCCATAACCCAGGAGAGCCA A G TNS2 Ensembl:ENSG00000111077 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:53052123..53052210 26863410 MeRIP-seq:(Medium) rs1041787761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125883,RMVar_hsa_circ_156844 90635 RMVar_ID_90635 Human_SNP_ID_501512640 m1A Human chr12 + 53054253 53054253 53054253 CCTCCGGGTGCCCCGCCCCTGCGTTCATGCGTAGGCTCCTCCTCCCCAGGAGCTTCAGCCTGGAC CCTCCGGGTGCCCCGCCCCTGCGTTCATGCGTGGGCTCCTCCTCCCCAGGAGCTTCAGCCTGGAC A G TNS2 Ensembl:ENSG00000111077 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53054251..53054382 26863196 MeRIP-seq:(Medium) rs1248672894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125883,RMVar_hsa_circ_156844,RMVar_hsa_circ_89279,RMVar_hsa_circ_98817,RMVar_hsa_circ_124886,RMVar_hsa_circ_156845,RMVar_hsa_circ_156846,RMVar_hsa_circ_359256,RMVar_hsa_circ_156847 90636 RMVar_ID_90636 Human_SNP_ID_501514617 m1A Human chr12 - 53059790 53059790 53059790 GTGCAGGAGAGGCTTGCCAGCCTCACTTGCCCACCCTTCTCCAGCCTCCCTCTCCAGCCGCAGTC GTGCAGGAGAGGCTTGCCAGCCTCACTTGCCCCCCCTTCTCCAGCCTCCCTCTCCAGCCGCAGTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53059742..53059870 32194978 MeRIP-seq:(Medium) rs949612401 Functional Loss SNV dbSNP153 33..33 33 - - - 90637 RMVar_ID_90637 Human_SNP_ID_501515082 m1A Human chr12 + 53061019 53061019 53061019 AGATGGGTCTCCCCTCACTCCTGTGCCTTCCCAGATGCCCTGGCTTGTGGCCAGCCCAGAGCCGC AGATGGGTCTCCCCTCACTCCTGTGCCTTCCCCGATGCCCTGGCTTGTGGCCAGCCCAGAGCCGC A C TNS2 Ensembl:ENSG00000111077 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53060968..53061060 26863196 MeRIP-seq:(Medium) rs201548222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811569,Human_RBP_ID_5127132,Human_RBP_ID_17074835 Human_miRNA_ID_1157123,Human_miRNA_ID_1347079,Human_miRNA_ID_1809410,Human_miRNA_ID_2675319,Human_miRNA_ID_2695803,Human_miRNA_ID_2926069 RMVar_hsa_circ_89279,RMVar_hsa_circ_77838,RMVar_hsa_circ_156845,RMVar_hsa_circ_112345,RMVar_hsa_circ_156851,RMVar_hsa_circ_156852,RMVar_hsa_circ_100180,RMVar_hsa_circ_156855 90638 RMVar_ID_90638 Human_SNP_ID_501515177 m1A Human chr12 + 53061244 53061244 53061244 TCACCATGTCACCTTCGCACCTCTGCTCTCAGATAATGTCCCCCAAACCCCAGGTATAAAGGCCT TCACCATGTCACCTTCGCACCTCTGCTCTCAGGTAATGTCCCCCAAACCCCAGGTATAAAGGCCT A G TNS2 Ensembl:ENSG00000111077 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53060946..53061280 26863196 MeRIP-seq:(Medium) rs543061160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1373167,Human_Splice_Rec_1373223,Human_Splice_Rec_1373301,Human_Splice_Rec_1373357,Human_Splice_Rec_1373411,Human_Splice_Rec_1373467,Human_Splice_Rec_1373525,Human_Splice_Rec_1373571 Human_miRNA_ID_2404044 RMVar_hsa_circ_89279,RMVar_hsa_circ_77838,RMVar_hsa_circ_156845,RMVar_hsa_circ_112345,RMVar_hsa_circ_156851,RMVar_hsa_circ_156852,RMVar_hsa_circ_100180,RMVar_hsa_circ_156855 90639 RMVar_ID_90639 Human_SNP_ID_501519370 m1A Human chr12 + 53077226 53077226 53077226 TCCGCCGGCGCCAATTCAGAAACCGGTAGTGCAGGTTGAGGTCATCCATCTTGTTCATGAGAACA TCCGCCGGCGCCAATTCAGAAACCGGTAGTGCCGGTTGAGGTCATCCATCTTGTTCATGAGAACA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr12:53077176..53077299;chr12:53077176..53077297;chr12:53077133..53077234 26863196,32194978 MeRIP-seq:(Medium) rs1305718385 Functional Loss SNV dbSNP153 33..33 33 - - - 90640 RMVar_ID_90640 Human_SNP_ID_501519373 m1A Human chr12 - 53077230 53077230 53077230 GGTTTGTTCTCATGAACAAGATGGATGACCTCAACCTGCACTACCGGTTTCTGAATTGGCGCCGG GGTTTGTTCTCATGAACAAGATGGATGACCTCTACCTGCACTACCGGTTTCTGAATTGGCGCCGG T A SPRYD3 Ensembl:ENSG00000167778 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53077189..53077297 26863196 MeRIP-seq:(Medium) rs761095798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1373596,Human_Splice_Rec_1373620,Human_Splice_Rec_1373640,Human_Splice_Rec_1373654 RMVar_hsa_circ_63722,RMVar_hsa_circ_156857,RMVar_hsa_circ_97674 90641 RMVar_ID_90641 Human_SNP_ID_501524198 m1A Human chr12 + 53097730 53097730 53097730 ACGGGGCACAAACCCTGACCATGACCCCCCACAGGCTGCTGCCACCGCTGCTGCTGCTGCTAGCT ACGGGGCACAAACCCTGACCATGACCCCCCACTGGCTGCTGCCACCGCTGCTGCTGCTGCTAGCT A T IGFBP6 Ensembl:ENSG00000167779 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53097679..53097924 26863196 MeRIP-seq:(Medium) rs1379178114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114434 Human_miRNA_ID_2756690 RMVar_hsa_circ_118330,RMVar_hsa_circ_156859 90642 RMVar_ID_90642 Human_SNP_ID_501524357 m1A Human chr12 - 53098050 53098050 53098050 TGGGCGGGGCAGGGGCGGGGCGCGGACTCACCAGCAGGCGCGCGGGCCGGAAGGCAGCGGCCTCG TGGGCGGGGCAGGGGCGGGGCGCGGACTCACCTGCAGGCGCGCGGGCCGGAAGGCAGCGGCCTCG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53097927..53099304 32194978 MeRIP-seq:(Medium) rs1002056412 Functional Loss SNV dbSNP153 33..33 33 - - - 90643 RMVar_ID_90643 Human_SNP_ID_501525037 m1A Human chr12 + 53100764 53100764 53100764 GAGAGTAAACCCCAAGCAGGCACTGCCCGCCCACAGGATGTGAACCGCAGAGACCAACAGAGGAA GAGAGTAAACCCCAAGCAGGCACTGCCCGCCCGCAGGATGTGAACCGCAGAGACCAACAGAGGAA A G IGFBP6 Ensembl:ENSG00000167779 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53100701..53100775 32194978 MeRIP-seq:(Medium) rs776345692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555420 Human_Splice_Rec_1373670,Human_Splice_Rec_1373671,Human_Splice_Rec_1373678,Human_Splice_Rec_1373679,Human_Splice_Rec_1373682,Human_Splice_Rec_1373683,Human_Splice_Rec_1373690,Human_Splice_Rec_1373691,Human_Splice_Rec_1373696,Human_Splice_Rec_1373697 RMVar_hsa_circ_118330,RMVar_hsa_circ_88234,RMVar_hsa_circ_156859,RMVar_hsa_circ_301996,RMVar_hsa_circ_156860 90644 RMVar_ID_90644 Human_SNP_ID_501525041 m1A Human chr12 + 53100775 53100775 53100775 CCAAGCAGGCACTGCCCGCCCACAGGATGTGAACCGCAGAGACCAACAGAGGAATCCAGGCACCT CCAAGCAGGCACTGCCCGCCCACAGGATGTGAGCCGCAGAGACCAACAGAGGAATCCAGGCACCT A G IGFBP6 Ensembl:ENSG00000167779 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53100676..53100778 26863196 MeRIP-seq:(Medium) rs138728327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555420 Human_Splice_Rec_1373670,Human_Splice_Rec_1373671,Human_Splice_Rec_1373678,Human_Splice_Rec_1373679,Human_Splice_Rec_1373682,Human_Splice_Rec_1373683,Human_Splice_Rec_1373690,Human_Splice_Rec_1373691,Human_Splice_Rec_1373696,Human_Splice_Rec_1373697 RMVar_hsa_circ_118330,RMVar_hsa_circ_88234,RMVar_hsa_circ_156859,RMVar_hsa_circ_301996,RMVar_hsa_circ_156860 90645 RMVar_ID_90645 Human_SNP_ID_501525516 m1A Human chr12 + 53102251 53102251 53102251 ATCACTCAACAAAAAACCGAGGCCCTCAATCCACCTTCAGGCCCCGCCCCATGGGCCCCTCACCG ATCACTCAACAAAAAACCGAGGCCCTCAATCCCCCTTCAGGCCCCGCCCCATGGGCCCCTCACCG A C IGFBP6 Ensembl:ENSG00000167779 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53102216..53102281 26863196 MeRIP-seq:(Medium) rs1053153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118330,RMVar_hsa_circ_88234,RMVar_hsa_circ_156859,RMVar_hsa_circ_99500,RMVar_hsa_circ_156860,RMVar_hsa_circ_82621,RMVar_hsa_circ_156861,RMVar_hsa_circ_156862 90646 RMVar_ID_90646 Human_SNP_ID_501547346 m1A Human chr12 + 53180569 53180569 53180569 TGCCCTCGGCGCACGGCGCCGCCCACTCACCCAGCTGCACCTCTCCGTGCGTCCCCAAGCTCACC TGCCCTCGGCGCACGGCGCCGCCCACTCACCCGGCTGCACCTCTCCGTGCGTCCCCAAGCTCACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53180295..53180628 26863196 MeRIP-seq:(Medium) rs1389562898 Functional Loss SNV dbSNP153 33..33 33 - - - 90647 RMVar_ID_90647 Human_SNP_ID_501547462 m1A Human chr12 + 53180750 53180750 53180750 GTTTGTAAACTTGCCTCGGTCCCGGTGGGGGCAGCCGCGGCGGTGGGGTTGGCAGGGTGTGCTGG GTTTGTAAACTTGCCTCGGTCCCGGTGGGGGCGGCCGCGGCGGTGGGGTTGGCAGGGTGTGCTGG A G ZNF740 Ensembl:ENSG00000139651 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:53180701..53180853;chr12:53180457..53181750;chr12:53180701..53180861 26863196 MeRIP-seq:(Medium) rs1490196725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230024,Human_RBP_ID_4246103,Human_RBP_ID_5522056,Human_RBP_ID_8787220,Human_RBP_ID_9352755,Human_RBP_ID_18417274,Human_RBP_ID_23564343 Human_Splice_Rec_1374071,Human_Splice_Rec_1374077 90648 RMVar_ID_90648 Human_SNP_ID_501547643 m1A Human chr12 + 53181139 53181139 53181139 CCGGCTCTGCTCCCGGTTGGTGCAGCGGGTGCAGAGGCTGGCTGGCCGGAGCGAGGCGGGCGACA CCGGCTCTGCTCCCGGTTGGTGCAGCGGGTGCCGAGGCTGGCTGGCCGGAGCGAGGCGGGCGACA A C ZNF740 Ensembl:ENSG00000139651 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53181137..53181307 26863196 MeRIP-seq:(Medium) rs1224841209 Functional Loss SNV dbSNP153 33..33 33 - - - 90649 RMVar_ID_90649 Human_SNP_ID_501547669 m1A Human chr12 + 53181214 53181214 53181214 GGCTTCGCCTGCCTGTCCTCCACCTCCGCAGCAAGTTTCCCTACCTTCGGGCGGACGGGGAGAAC GGCTTCGCCTGCCTGTCCTCCACCTCCGCAGCGAGTTTCCCTACCTTCGGGCGGACGGGGAGAAC A G ZNF740 Ensembl:ENSG00000139651 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53181211..53181299 26863196 MeRIP-seq:(Medium) rs1006527459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4228011 90650 RMVar_ID_90650 Human_SNP_ID_501550281 m1A Human chr12 + 53190160 53190160 53190160 TTCAGTTCCCGCGCTGATGTCTGGGGCAGTGCATGTGTGAGAAGAGAGGCGCAAAGCAGTGAAAG TTCAGTTCCCGCGCTGATGTCTGGGGCAGTGCCTGTGTGAGAAGAGAGGCGCAAAGCAGTGAAAG A C ZNF740 Ensembl:ENSG00000139651 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53190110..53190195 26863196 MeRIP-seq:(Medium) rs1347135363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_422156,Human_RBP_ID_4228168,Human_RBP_ID_5111709,Human_RBP_ID_6196066,Human_RBP_ID_8782736,Human_RBP_ID_23564429,Human_RBP_ID_26421236 Human_miRNA_ID_1475170,Human_miRNA_ID_1480129 90651 RMVar_ID_90651 Human_SNP_ID_501550394 m1A Human chr12 + 53190532 53190532 53190532 CCCCCAACAGCCTTGTCATCACTTAGCTACTGATCACGCCCATGGCTTGACATTGGAGGGTTACA CCCCCAACAGCCTTGTCATCACTTAGCTACTGGTCACGCCCATGGCTTGACATTGGAGGGTTACA A G ZNF740 Ensembl:ENSG00000139651 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53190487..53190602 26863196 MeRIP-seq:(Medium) rs1202144811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_422161,Human_RBP_ID_992873,Human_RBP_ID_3408242,Human_RBP_ID_4228186,Human_RBP_ID_6196084,Human_RBP_ID_11973747,Human_RBP_ID_17075534,Human_RBP_ID_23564433,Human_RBP_ID_26422256 Human_miRNA_ID_830639,Human_miRNA_ID_1186339 90652 RMVar_ID_90652 Human_SNP_ID_501558999 m1A Human chr12 + 53221133 53221133 53221133 TCCTCCTGACCCGGCCCCGCCCCACCCCGCCCAGGCCGTCTTCAGCGCTGCCGCGGAGTCCCCCC TCCTCCTGACCCGGCCCCGCCCCACCCCGCCCCGGCCGTCTTCAGCGCTGCCGCGGAGTCCCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53221122..53221231 26863196 MeRIP-seq:(Medium) rs1317717052 Functional Loss SNV dbSNP153 33..33 33 - - - 90653 RMVar_ID_90653 Human_SNP_ID_501559000 m1A Human chr12 + 53221133 53221133 53221133 TCCTCCTGACCCGGCCCCGCCCCACCCCGCCCAGGCCGTCTTCAGCGCTGCCGCGGAGTCCCCCC TCCTCCTGACCCGGCCCCGCCCCACCCCGCCCTGGCCGTCTTCAGCGCTGCCGCGGAGTCCCCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53221122..53221231 26863196 MeRIP-seq:(Medium) rs1317717052 Functional Loss SNV dbSNP153 33..33 33 - - - 90654 RMVar_ID_90654 Human_SNP_ID_501560780 m1A Human chr12 - 53227665 53227665 53227665 TTCTCCCTAGGACTTTTGGAGGCCCAGTGGGCAGGCCAGGCAGGGCGGGTACGGAGCCTCCCAGG TTCTCCCTAGGACTTTTGGAGGCCCAGTGGGCGGGCCAGGCAGGGCGGGTACGGAGCCTCCCAGG T C RARG Ensembl:ENSG00000172819 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53227427..53227722 26863196 MeRIP-seq:(Medium) rs1189961484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1374264,Human_Splice_Rec_1374338,Human_Splice_Rec_1374344,Human_Splice_Rec_1374350,Human_Splice_Rec_1374356,Human_Splice_Rec_1374362,Human_Splice_Rec_1374368,Human_Splice_Rec_1374374,Human_Splice_Rec_1374380 90655 RMVar_ID_90655 Human_SNP_ID_501560781 m1A Human chr12 - 53227665 53227665 53227665 TTCTCCCTAGGACTTTTGGAGGCCCAGTGGGCAGGCCAGGCAGGGCGGGTACGGAGCCTCCCAGG TTCTCCCTAGGACTTTTGGAGGCCCAGTGGGCCGGCCAGGCAGGGCGGGTACGGAGCCTCCCAGG T G RARG Ensembl:ENSG00000172819 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53227427..53227722 26863196 MeRIP-seq:(Medium) rs1189961484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1374264,Human_Splice_Rec_1374338,Human_Splice_Rec_1374344,Human_Splice_Rec_1374350,Human_Splice_Rec_1374356,Human_Splice_Rec_1374362,Human_Splice_Rec_1374368,Human_Splice_Rec_1374374,Human_Splice_Rec_1374380 90656 RMVar_ID_90656 Human_SNP_ID_501560788 m1A Human chr12 - 53227689 53227689 53227689 CTCTCATCTCTCCTTTCTCTCTCTTTCTCCCTAGGACTTTTGGAGGCCCAGTGGGCAGGCCAGGC CTCTCATCTCTCCTTTCTCTCTCTTTCTCCCTGGGACTTTTGGAGGCCCAGTGGGCAGGCCAGGC T C RARG Ensembl:ENSG00000172819 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53227640..53227719 26863196 MeRIP-seq:(Medium) rs1314269952 Functional Loss SNV dbSNP153 33..33 33 - - - 90657 RMVar_ID_90657 Human_SNP_ID_501561625 m1A Human chr12 - 53231223 53231223 53231223 CGCTGCCTCTCTGTCTTTAGCAGCTACGGCCCAGTTCCCTCAACCTGACCCAGTATGTAGAAGCC CGCTGCCTCTCTGTCTTTAGCAGCTACGGCCCGGTTCCCTCAACCTGACCCAGTATGTAGAAGCC T C RARG Ensembl:ENSG00000172819 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53230059..53231407 26863196 MeRIP-seq:(Medium) rs1476380365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_422179 Human_Splice_Rec_1374246,Human_Splice_Rec_1374247,Human_Splice_Rec_1374262,Human_Splice_Rec_1374263,Human_Splice_Rec_1374306,Human_Splice_Rec_1374307,Human_Splice_Rec_1374342,Human_Splice_Rec_1374343,Human_Splice_Rec_1374348,Human_Splice_Rec_1374349,Human_Splice_Rec_1374354,Human_Splice_Rec_1374355,Human_Splice_Rec_1374358,Human_Splice_Rec_1374359,Human_Splice_Rec_1374364,Human_Splice_Rec_1374365,Human_Splice_Rec_1374370,Human_Splice_Rec_1374371,Human_Splice_Rec_1374376,Human_Splice_Rec_1374377,Human_Splice_Rec_1374386 90658 RMVar_ID_90658 Human_SNP_ID_501561787 m1A Human chr12 + 53231938 53231938 53231938 TCCCCCAGCCGCCTCGCCGGAGGACCCAGGCGACGGGGCGGGCGAGCCTGCTTCCCCGCCTGACT TCCCCCAGCCGCCTCGCCGGAGGACCCAGGCGGCGGGGCGGGCGAGCCTGCTTCCCCGCCTGACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53231936..53232220 26863196 MeRIP-seq:(Medium) rs1452811167 Functional Loss SNV dbSNP153 33..33 33 - - - 90659 RMVar_ID_90659 Human_SNP_ID_501561803 m1A Human chr12 - 53231980 53231974 53231980 CTCGGGGCTCCGCCGCCTCCCTTCCCCCTCCCACTCCAGGTGAGTCAGGCGGGGAAGCAGGCTCG CTCGGGGCTCCGCCGCCTCCCTTCCCCCTCCC______GGTGAGTCAGGCGGGGAAGCAGGCTCG CTGGAGT C RARG Ensembl:ENSG00000172819 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53231978..53232129 32194978 MeRIP-seq:(Medium) rs1358573962 Functional Loss DEL dbSNP153 33..38 33 - - - Human_Splice_Rec_1374245,Human_Splice_Rec_1374261,Human_Splice_Rec_1374305,Human_Splice_Rec_1374337,Human_Splice_Rec_1374341,Human_Splice_Rec_1374347,Human_Splice_Rec_1374353,Human_Splice_Rec_1374357,Human_Splice_Rec_1374363,Human_Splice_Rec_1374369,Human_Splice_Rec_1374375,Human_Splice_Rec_1374383 90660 RMVar_ID_90660 Human_SNP_ID_501566520 m1A Human chr12 + 53251318 53251310 53251318 AGAGGAGCAGGGGATGAAGTCAGAGGAGTGGCAGAGGGTCAGAGGACAGAGGGTCTTGTAGGCCA AGAGGAGCAGGGGATGAAGTCAGAG________GAGGGTCAGAGGACAGAGGGTCTTGTAGGCCA GGAGTGGCA G MFSD5 Ensembl:ENSG00000182544 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53251282..53251376 26863196 MeRIP-seq:(Medium) rs1003735795 Functional Loss DEL dbSNP153 26..33 33 - - - 90661 RMVar_ID_90661 Human_SNP_ID_501571306 m1A Human chr12 - 53268339 53268339 53268339 AGAGCTCGCCCTCTTTCCTAGGTACAGGACTTAACCGCCTGACCAGTACTCCGCGAGGATCCAAA AGAGCTCGCCCTCTTTCCTAGGTACAGGACTTCACCGCCTGACCAGTACTCCGCGAGGATCCAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53268289..53268514 26863196 MeRIP-seq:(Medium) rs1274282392 Functional Loss SNV dbSNP153 33..33 33 - - - 90662 RMVar_ID_90662 Human_SNP_ID_501571313 m1A Human chr12 + 53268358 53268358 53268358 CTGGTCAGGCGGTTAAGTCCTGTACCTAGGAAAGAGGGCGAGCTCTGGGGCGGTAAGGCCGGAAG CTGGTCAGGCGGTTAAGTCCTGTACCTAGGAAGGAGGGCGAGCTCTGGGGCGGTAAGGCCGGAAG A G ESPL1 Ensembl:ENSG00000135476 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53268308..53268606 26863196 MeRIP-seq:(Medium) rs977566633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417275 Human_Splice_Rec_1374397,Human_Splice_Rec_1374457,Human_Splice_Rec_1374517 Human_miRNA_ID_2569409 RMVar_hsa_circ_98134,RMVar_hsa_circ_156887 90663 RMVar_ID_90663 Human_SNP_ID_501572411 m1A Human chr12 + 53272299 53272299 53272299 AGAAATGTGGGGGAAAGGAAAAGTAGAGCAGGATAAGAAAGGGAATTGGGAGTCTAAGGTGCATG AGAAATGTGGGGGAAAGGAAAAGTAGAGCAGGTTAAGAAAGGGAATTGGGAGTCTAAGGTGCATG A T ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53272295..53272418 26863196 MeRIP-seq:(Medium) rs1303847665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973899 RMVar_hsa_circ_98134,RMVar_hsa_circ_123069,RMVar_hsa_circ_156887,RMVar_hsa_circ_156888,RMVar_hsa_circ_156891,RMVar_hsa_circ_95443,RMVar_hsa_circ_106244,RMVar_hsa_circ_78559,RMVar_hsa_circ_156892,RMVar_hsa_circ_156890,RMVar_hsa_circ_156893,RMVar_hsa_circ_370223 90664 RMVar_ID_90664 Human_SNP_ID_501572969 m1A Human chr12 - 53274368 53274368 53274368 AGCCCACCCTTCCCTGCCTAGAATACTATAGCAGCCTGATTACCCGGTCTTTTCTCCTGCACTCC AGCCCACCCTTCCCTGCCTAGAATACTATAGCGGCCTGATTACCCGGTCTTTTCTCCTGCACTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:53274317..53274486 26863196 MeRIP-seq:(Medium) rs1213397208 Functional Loss SNV dbSNP153 33..33 33 - - - 90665 RMVar_ID_90665 Human_SNP_ID_501576500 m1A Human chr12 - 53288235 53288235 53288235 TCCTCAGGGATGGTCCTCATGATCTCAGGGCCAGGCCTGGCCTGGTCACTGGCCCTCTGGGGACG TCCTCAGGGATGGTCCTCATGATCTCAGGGCCGGGCCTGGCCTGGTCACTGGCCCTCTGGGGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53288184..53288255 26863196 MeRIP-seq:(Medium) rs1442738716 Functional Loss SNV dbSNP153 33..33 33 - - - 90666 RMVar_ID_90666 Human_SNP_ID_501578559 m1A Human chr12 - 53295600 53295600 53295600 AGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCCAT AGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGTTTCAGCTCCGTGATGTTAATAGACTGCGCCAT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53295551..53295688 26863196 MeRIP-seq:(Medium) rs981316141 Functional Loss SNV dbSNP153 33..33 33 - - - 90667 RMVar_ID_90667 Human_SNP_ID_501578560 m1A Human chr12 - 53295602 53295601 53295602 CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCC CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGC_GATTCAGCTCCGTGATGTTAATAGACTGCGCC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53295526..53295679;chr12:53295551..53295625 26863196 MeRIP-seq:(Medium) rs1366049388 Functional Loss DEL dbSNP153 33..33 33 - - - 90668 RMVar_ID_90668 Human_SNP_ID_501578561 m1A Human chr12 - 53295602 53295602 53295602 CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCC CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCGGATTCAGCTCCGTGATGTTAATAGACTGCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53295526..53295679;chr12:53295551..53295625 26863196 MeRIP-seq:(Medium) rs199718276 Functional Loss SNV dbSNP153 33..33 33 - - - 90669 RMVar_ID_90669 Human_SNP_ID_501578562 m1A Human chr12 - 53295602 53295602 53295602 CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCC CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCCGATTCAGCTCCGTGATGTTAATAGACTGCGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53295526..53295679;chr12:53295551..53295625 26863196 MeRIP-seq:(Medium) rs199718276 Functional Loss SNV dbSNP153 33..33 33 - - - 90670 RMVar_ID_90670 Human_SNP_ID_501578582 m1A Human chr12 + 53295638 53295638 53295638 GCAGCTAGAAATGCTCAAGAACCAGCTGGACCAGGTGGGGACGGGCCCCAGAGGCACCTCTTTCC GCAGCTAGAAATGCTCAAGAACCAGCTGGACCGGGTGGGGACGGGCCCCAGAGGCACCTCTTTCC A G PFDN5 Ensembl:ENSG00000123349 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53295588..53295689 32194978 MeRIP-seq:(Medium) rs1224127966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111714,Human_RBP_ID_19056235,Human_RBP_ID_22437088 Human_Splice_Rec_1374571,Human_Splice_Rec_1374581,Human_Splice_Rec_1374583,Human_Splice_Rec_1374591,Human_Splice_Rec_1374597,Human_Splice_Rec_1374599,Human_Splice_Rec_1374603,Human_Splice_Rec_1374607,Human_Splice_Rec_1374615,Human_Splice_Rec_1374623,Human_Splice_Rec_1374631,Human_Splice_Rec_1374641,Human_Splice_Rec_1374645,Human_Splice_Rec_1374655,Human_Splice_Rec_1374659 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_26717,RMVar_hsa_circ_156904 90671 RMVar_ID_90671 Human_SNP_ID_501578816 m1A Human chr12 - 53296275 53296275 53296275 GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACAGAACTCGTCAGTGGGACGAGTAATTCTTTCCC GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACTGAACTCGTCAGTGGGACGAGTAATTCTTTCCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53296234..53296384 32194978 MeRIP-seq:(Medium) rs760941908 Functional Loss SNV dbSNP153 33..33 33 - - - 90672 RMVar_ID_90672 Human_SNP_ID_501578817 m1A Human chr12 - 53296275 53296275 53296275 GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACAGAACTCGTCAGTGGGACGAGTAATTCTTTCCC GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACGGAACTCGTCAGTGGGACGAGTAATTCTTTCCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53296234..53296384 32194978 MeRIP-seq:(Medium) rs760941908 Functional Loss SNV dbSNP153 33..33 33 - - - 90673 RMVar_ID_90673 Human_SNP_ID_501579668 m1A Human chr12 - 53299234 53299234 53299234 GTGGAAAAAAATAAGAGTCAAAGGTTAGAAGCAAAAAGGAGAACCTAGAGTTAAGGAGAAGTGAC GTGGAAAAAAATAAGAGTCAAAGGTTAGAAGCGAAAAGGAGAACCTAGAGTTAAGGAGAAGTGAC T C AC073611.1 Ensembl:ENSG00000257605 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53299231..53299388 26863196 MeRIP-seq:(Medium) rs754103896 Functional Loss SNV dbSNP153 33..33 33 - - - 90674 RMVar_ID_90674 Human_SNP_ID_501579734 m1A Human chr12 + 53299406 53299406 53299406 CACCCTTTGGGCGTGGCTTCCTGGTGATGGGAAGGGTCTTGTGTTTTAATGCCAATAAATGTGCC CACCCTTTGGGCGTGGCTTCCTGGTGATGGGAGGGGTCTTGTGTTTTAATGCCAATAAATGTGCC A G PFDN5 Ensembl:ENSG00000123349 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53299376..53299450 32194978 MeRIP-seq:(Medium) rs777490899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34499,Human_RBP_ID_228862,Human_RBP_ID_422229,Human_RBP_ID_1357842,Human_RBP_ID_1473402,Human_RBP_ID_1796891,Human_RBP_ID_3408282,Human_RBP_ID_3942969,Human_RBP_ID_5111954,Human_RBP_ID_5139855,Human_RBP_ID_8378678,Human_RBP_ID_9322523,Human_RBP_ID_9364963,Human_RBP_ID_17649983,Human_RBP_ID_17830835,Human_RBP_ID_18188791,Human_RBP_ID_18628715,Human_RBP_ID_22437725,Human_RBP_ID_23207642 RMVar_hsa_circ_106127,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_84713,RMVar_hsa_circ_156908,RMVar_hsa_circ_156909 90675 RMVar_ID_90675 Human_SNP_ID_501579927 m1A Human chr12 - 53299775 53299775 53299775 GGTGCCGGGTATACAGGGGTGGCGGCGGCAGCAGCAGCGTTAAGAGGCCGCGCAGGAATTGGTGT GGTGCCGGGTATACAGGGGTGGCGGCGGCAGCGGCAGCGTTAAGAGGCCGCGCAGGAATTGGTGT T C AC073611.1 Ensembl:ENSG00000257605 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53299726..53299900 26863196 MeRIP-seq:(Medium) rs1383948298 Functional Loss SNV dbSNP153 33..33 33 - - - 90676 RMVar_ID_90676 Human_SNP_ID_501579933 m1A Human chr12 + 53299798 53299782 53299799 TAACGCTGCTGCTGCCGCCGCCACCCCTGTATACCCGGCACCGCATGCTCGGTCCAGAGTCCGTC TAACGCTGCTGCTGCCG_________________CCGGCACCGCATGCTCGGTCCAGAGTCCGTC GCCGCCACCCCTGTATAC G C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53299751..53299881 26863196 MeRIP-seq:(Medium) rs1280954485 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_4228501 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910 90677 RMVar_ID_90677 Human_SNP_ID_501579998 m1A Human chr12 + 53299855 53299855 53299855 AGTCCGTCCCGCCCCCAAAACGATCCCGCAGCAAACTCATGGCACCGCCCCGAATCGGGACGCAC AGTCCGTCCCGCCCCCAAAACGATCCCGCAGCTAACTCATGGCACCGCCCCGAATCGGGACGCAC A T C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:53299701..53299900 26863196 MeRIP-seq:(Medium) rs1444368381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1374685,Human_Splice_Rec_1374707,Human_Splice_Rec_1374711 Human_miRNA_ID_2388403,Human_miRNA_ID_2399553,Human_miRNA_ID_3030607 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910 90678 RMVar_ID_90678 Human_SNP_ID_501580030 m1A Human chr12 - 53299921 53299921 53299921 CCGGTACTCCGGCAGGAGGCGAAGCAGTGCGCATGCCAGTGCCTCGTCGCAGTGGAAGGTGCCAT CCGGTACTCCGGCAGGAGGCGAAGCAGTGCGCTTGCCAGTGCCTCGTCGCAGTGGAAGGTGCCAT T A AC073611.1 Ensembl:ENSG00000257605 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53299783..53299950 32194978 MeRIP-seq:(Medium) rs143220786 Functional Loss SNV dbSNP153 33..33 33 - - - 90679 RMVar_ID_90679 Human_SNP_ID_501580031 m1A Human chr12 - 53299921 53299921 53299921 CCGGTACTCCGGCAGGAGGCGAAGCAGTGCGCATGCCAGTGCCTCGTCGCAGTGGAAGGTGCCAT CCGGTACTCCGGCAGGAGGCGAAGCAGTGCGCGTGCCAGTGCCTCGTCGCAGTGGAAGGTGCCAT T C AC073611.1 Ensembl:ENSG00000257605 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53299783..53299950 32194978 MeRIP-seq:(Medium) rs143220786 Functional Loss SNV dbSNP153 33..33 33 - - - 90680 RMVar_ID_90680 Human_SNP_ID_501580870 m1A Human chr12 - 53303135 53303135 53303135 TGTCCTCTTCACTAGTGCCCAGCAACTGGGCCAGCAGCTTGTGCCCGAAGTGCAGATAGATGAGT TGTCCTCTTCACTAGTGCCCAGCAACTGGGCCGGCAGCTTGTGCCCGAAGTGCAGATAGATGAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53303086..53303230 26863196 MeRIP-seq:(Medium) rs146471867 Functional Loss SNV dbSNP153 33..33 33 - - - 90681 RMVar_ID_90681 Human_SNP_ID_501581664 m1A Human chr12 - 53306057 53306057 53306057 TCTCCGGGTCTCCTCCCAGGCCACCTTACCTCAGTGTCTTGGTCGGGGTGGTTCCAGGTAGGATT TCTCCGGGTCTCCTCCCAGGCCACCTTACCTCCGTGTCTTGGTCGGGGTGGTTCCAGGTAGGATT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53305868..53306086 26863196 MeRIP-seq:(Medium) rs1286122816 Functional Loss SNV dbSNP153 33..33 33 - - - 90682 RMVar_ID_90682 Human_SNP_ID_501581863 m1A Human chr12 - 53306681 53306681 53306681 TCGCCAGTTCCACAATCTCTCCACTTGGGTCCACCTGAAAGAGGGAGAGCATAGCTAGAAGGTTT TCGCCAGTTCCACAATCTCTCCACTTGGGTCCGCCTGAAAGAGGGAGAGCATAGCTAGAAGGTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53306679..53306778 32194978 MeRIP-seq:(Medium) rs1041729659 Functional Loss SNV dbSNP153 33..33 33 - - - 90683 RMVar_ID_90683 Human_SNP_ID_501582035 m1A Human chr12 + 53307076 53307075 53307076 CGTCCATGCAAGCGGCTTCACTGGCGGTCACCACACCCGAGAGGGTGCCTTGAGCATGGCCCGTG CGTCCATGCAAGCGGCTTCACTGGCGGTCACC_CACCCGAGAGGGTGCCTTGAGCATGGCCCGTG CA C C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53307026..53307115 26863196 MeRIP-seq:(Medium) rs1565775255 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24365577 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910,RMVar_hsa_circ_100229,RMVar_hsa_circ_109576,RMVar_hsa_circ_156912,RMVar_hsa_circ_156913 90684 RMVar_ID_90684 Human_SNP_ID_501582036 m1A Human chr12 + 53307076 53307076 53307076 CGTCCATGCAAGCGGCTTCACTGGCGGTCACCACACCCGAGAGGGTGCCTTGAGCATGGCCCGTG CGTCCATGCAAGCGGCTTCACTGGCGGTCACCGCACCCGAGAGGGTGCCTTGAGCATGGCCCGTG A G C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53307026..53307115 26863196 MeRIP-seq:(Medium) rs711316 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_24365577 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910,RMVar_hsa_circ_100229,RMVar_hsa_circ_109576,RMVar_hsa_circ_156912,RMVar_hsa_circ_156913 90685 RMVar_ID_90685 Human_SNP_ID_501582230 m1A Human chr12 + 53307615 53307615 53307615 GGCAGGTCATGAATAGAGCCTCCACCCCCAGCAGGGGGTTCCTGGGCCCGCCCAAGCACTGGGCT GGCAGGTCATGAATAGAGCCTCCACCCCCAGCGGGGGGTTCCTGGGCCCGCCCAAGCACTGGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53307564..53307639 26863196 MeRIP-seq:(Medium) rs35282133 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_510,Clinvar_Rec_511 90686 RMVar_ID_90686 Human_SNP_ID_501582352 m1A Human chr12 - 53307931 53307931 53307931 TTGCCTCCGGTTGCCTGCTCACCTTTTCTTCTAGTGGCATTATCCAGGGGGAGCCAGGAGCCCAG TTGCCTCCGGTTGCCTGCTCACCTTTTCTTCTTGTGGCATTATCCAGGGGGAGCCAGGAGCCCAG T A AAAS Ensembl:ENSG00000094914 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53307778..53308078 32194978 MeRIP-seq:(Medium) rs1565776390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18160505,Human_RBP_ID_22644847 Human_Splice_Rec_1374789,Human_Splice_Rec_1374817,Human_Splice_Rec_1374845,Human_Splice_Rec_1374875,Human_Splice_Rec_1374903,Human_Splice_Rec_1374945,Human_Splice_Rec_1374971,Human_Splice_Rec_1374999,Human_Splice_Rec_1375025,Human_Splice_Rec_1375047,Human_Splice_Rec_1375075 RMVar_hsa_circ_81648,RMVar_hsa_circ_106566,RMVar_hsa_circ_122221,RMVar_hsa_circ_92940,RMVar_hsa_circ_103343,RMVar_hsa_circ_85555,RMVar_hsa_circ_100652,RMVar_hsa_circ_156917,RMVar_hsa_circ_77814,RMVar_hsa_circ_79619,RMVar_hsa_circ_156919,RMVar_hsa_circ_156921,RMVar_hsa_circ_156922,RMVar_hsa_circ_156920,RMVar_hsa_circ_156918,RMVar_hsa_circ_156915,RMVar_hsa_circ_156916,RMVar_hsa_circ_266154,RMVar_hsa_circ_156923 90687 RMVar_ID_90687 Human_SNP_ID_501582494 m1A Human chr12 + 53308326 53308326 53308326 CAGCCAGACGTTCCCCACTGGGGTCCCAGACCATGGAGTGAGCCTCTCCCCCAAGCCTGTGGGTA CAGCCAGACGTTCCCCACTGGGGTCCCAGACCGTGGAGTGAGCCTCTCCCCCAAGCCTGTGGGTA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53308127..53308461 32194978 MeRIP-seq:(Medium) rs1050403276 Functional Loss SNV dbSNP153 33..33 33 - - - 90688 RMVar_ID_90688 Human_SNP_ID_501582574 m1A Human chr12 + 53308503 53308503 53308503 GACAGATCTGCCACAATCGTTGCTGACTTTGCACCTCCAACGCACCCCTTTCCCTCACCTGTGGA GACAGATCTGCCACAATCGTTGCTGACTTTGCCCCTCCAACGCACCCCTTTCCCTCACCTGTGGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53308404..53308508 26863196 MeRIP-seq:(Medium) rs749645216 Functional Loss SNV dbSNP153 33..33 33 - - - 90689 RMVar_ID_90689 Human_SNP_ID_501584281 m1A Human chr12 + 53314428 53314427 53314428 CGCCACATTTCGCTGCAGCCGGTGCTTCAGGGAGGGGACTATGGTGCTAGGGTGAAGGGGCAGGA CGCCACATTTCGCTGCAGCCGGTGCTTCAGGG_GGGGACTATGGTGCTAGGGTGAAGGGGCAGGA GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53314326..53314493 26863196 MeRIP-seq:(Medium) rs1280789199 Functional Loss DEL dbSNP153 33..33 33 - - - 90690 RMVar_ID_90690 Human_SNP_ID_501584283 m1A Human chr12 + 53314428 53314428 53314428 CGCCACATTTCGCTGCAGCCGGTGCTTCAGGGAGGGGACTATGGTGCTAGGGTGAAGGGGCAGGA CGCCACATTTCGCTGCAGCCGGTGCTTCAGGGGGGGGACTATGGTGCTAGGGTGAAGGGGCAGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53314326..53314493 26863196 MeRIP-seq:(Medium) rs1366368470 Functional Loss SNV dbSNP153 33..33 33 - - - 90691 RMVar_ID_90691 Human_SNP_ID_501586258 m1A Human chr12 - 53321111 53321111 53321111 GTGGAGGAGGCCTAGAGGGAATGGAGAGAATGAGGGAGAATCTAGGGAGTGTGAGGATGCGGGAG GTGGAGGAGGCCTAGAGGGAATGGAGAGAATGGGGGAGAATCTAGGGAGTGTGAGGATGCGGGAG T C AAAS Ensembl:ENSG00000094914 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53321078..53321226 26863196 MeRIP-seq:(Medium) rs1039412953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811614,Human_RBP_ID_9344520,Human_RBP_ID_18934485,Human_RBP_ID_22471965,Human_RBP_ID_22905174,Human_RBP_ID_23564545 RMVar_hsa_circ_77814,RMVar_hsa_circ_156922 90692 RMVar_ID_90692 Human_SNP_ID_501586401 m1A Human chr12 + 53321450 53321447 53321451 GACTTGACCCCGAGGCGGTGGAGGAGGGAACAACCCCAGAGAGCACATCTTGCCGGTTCGCAGGA GACTTGACCCCGAGGCGGTGGAGGAGGGAA____CCCAGAGAGCACATCTTGCCGGTTCGCAGGA ACAAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53321401..53321557 26863196 MeRIP-seq:(Medium) rs1483793303 Functional Loss DEL dbSNP153 31..34 33 - - - 90693 RMVar_ID_90693 Human_SNP_ID_501586403 m1A Human chr12 + 53321450 53321450 53321450 GACTTGACCCCGAGGCGGTGGAGGAGGGAACAACCCCAGAGAGCACATCTTGCCGGTTCGCAGGA GACTTGACCCCGAGGCGGTGGAGGAGGGAACAGCCCCAGAGAGCACATCTTGCCGGTTCGCAGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53321401..53321557 26863196 MeRIP-seq:(Medium) rs761552347 Functional Loss SNV dbSNP153 33..33 33 - - - 90694 RMVar_ID_90694 Human_SNP_ID_501586438 m1A Human chr12 + 53321521 53321521 53321521 CAGTCGGCAAACTCCTGGCCGGAACGGCACAGACCGCACTCCCGCAACTCGGTTCCCGGGCTAGA CAGTCGGCAAACTCCTGGCCGGAACGGCACAGTCCGCACTCCCGCAACTCGGTTCCCGGGCTAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53321026..53321575 26863196 MeRIP-seq:(Medium) rs1436442175 Functional Loss SNV dbSNP153 33..33 33 - - - 90695 RMVar_ID_90695 Human_SNP_ID_501602245 m1A Human chr12 - 53380850 53380849 53380850 AAAAACATTTGTGAATACTGCTAAGGAACTAAAGGGATCTACAGGTTAGTAGTCAGAAGGTTTCG AAAAACATTTGTGAATACTGCTAAGGAACTAA_GGGATCTACAGGTTAGTAGTCAGAAGGTTTCG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53380840..53380905 26863196 MeRIP-seq:(Medium) rs1259288162 Functional Loss DEL dbSNP153 33..33 33 - - - 90696 RMVar_ID_90696 Human_SNP_ID_501602247 m1A Human chr12 - 53380850 53380850 53380850 AAAAACATTTGTGAATACTGCTAAGGAACTAAAGGGATCTACAGGTTAGTAGTCAGAAGGTTTCG AAAAACATTTGTGAATACTGCTAAGGAACTAAGGGGATCTACAGGTTAGTAGTCAGAAGGTTTCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53380840..53380905 26863196 MeRIP-seq:(Medium) rs1205135666 Functional Loss SNV dbSNP153 33..33 33 - - - 90697 RMVar_ID_90697 Human_SNP_ID_501603066 m1A Human chr12 - 53383075 53383075 53383075 TCTTTTTGCTGGCCTGCTTGCAATGAGCCTCCAGATGTCTGGTTTTGCTGGATGTTCAGAGCATC TCTTTTTGCTGGCCTGCTTGCAATGAGCCTCCCGATGTCTGGTTTTGCTGGATGTTCAGAGCATC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53383024..53383125 32194978 MeRIP-seq:(Medium) rs773297185 Functional Loss SNV dbSNP153 33..33 33 - - - 90698 RMVar_ID_90698 Human_SNP_ID_501603120 m1A Human chr12 + 53383242 53383242 53383242 AGGGCAGACCTTTACAACTCAAGCCATCTCCCAGGAAACCCTCCAGAACCTCCAGCTTCAGGCTG AGGGCAGACCTTTACAACTCAAGCCATCTCCCGGGAAACCCTCCAGAACCTCCAGCTTCAGGCTG A G SP1 Ensembl:ENSG00000185591 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53383191..53383315 26863196 MeRIP-seq:(Medium) rs1240477564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1796908,Human_RBP_ID_17239073,Human_RBP_ID_17354803,Human_RBP_ID_17471930,Human_RBP_ID_18628735,Human_RBP_ID_27422978 Human_miRNA_ID_2040313,Human_miRNA_ID_2040314,Human_miRNA_ID_2040315,Human_miRNA_ID_2793004,Human_miRNA_ID_2793005,Human_miRNA_ID_2793006,Human_miRNA_ID_3019294,Human_miRNA_ID_3019295,Human_miRNA_ID_3019296 RMVar_hsa_circ_81010,RMVar_hsa_circ_156934,RMVar_hsa_circ_85364,RMVar_hsa_circ_108173,RMVar_hsa_circ_156935,RMVar_hsa_circ_156936,RMVar_hsa_circ_78974,RMVar_hsa_circ_156938,RMVar_hsa_circ_305340,RMVar_hsa_circ_315418,RMVar_hsa_circ_156937,RMVar_hsa_circ_156939 90699 RMVar_ID_90699 Human_SNP_ID_501611550 m1A Human chr12 + 53411105 53411105 53411105 GGTTCAGAAGGCAGTGGCACTGCCACTCCTTCAGCCCTTATTACCACCAATATGGTAGCCATGGA GGTTCAGAAGGCAGTGGCACTGCCACTCCTTCGGCCCTTATTACCACCAATATGGTAGCCATGGA A G SP1 Ensembl:ENSG00000185591 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53411057..53411258 32194978 MeRIP-seq:(Medium) rs1470611242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9278161,Human_RBP_ID_27630420 RMVar_hsa_circ_108173,RMVar_hsa_circ_156935 90700 RMVar_ID_90700 Human_SNP_ID_501612068 m1A Human chr12 + 53412985 53412985 53412985 TGTGTGTGTGTGTGTAATCTGTTAGGTTGGGGATAGGTTTTCTGCTAGCCAATATTAAAAGAGAC TGTGTGTGTGTGTGTAATCTGTTAGGTTGGGGGTAGGTTTTCTGCTAGCCAATATTAAAAGAGAC A G SP1 Ensembl:ENSG00000185591 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53412853..53413054 32194978 MeRIP-seq:(Medium) rs917620270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275447,Human_RBP_ID_422290,Human_RBP_ID_992957,Human_RBP_ID_2343249,Human_RBP_ID_3408319,Human_RBP_ID_4247474,Human_RBP_ID_5283760,Human_RBP_ID_5644589,Human_RBP_ID_6196371,Human_RBP_ID_8179158,Human_RBP_ID_8782939,Human_RBP_ID_8946470,Human_RBP_ID_9018267,Human_RBP_ID_9278177,Human_RBP_ID_11974752,Human_RBP_ID_17239108,Human_RBP_ID_17821740,Human_RBP_ID_18261495,Human_RBP_ID_18434367,Human_RBP_ID_23113276,Human_RBP_ID_23564609,Human_RBP_ID_24466767,Human_RBP_ID_24979330,Human_RBP_ID_26421252,Human_RBP_ID_27630473 RMVar_hsa_circ_108173,RMVar_hsa_circ_156935 90701 RMVar_ID_90701 Human_SNP_ID_501612556 m1A Human chr12 + 53415015 53415015 53415015 AGCTGGGTAGCCTATTGGGGTTGAGAGGGAAAATGTGAAATCTCAGAATTTATCTCCCTTAGAAG AGCTGGGTAGCCTATTGGGGTTGAGAGGGAAAGTGTGAAATCTCAGAATTTATCTCCCTTAGAAG A G SP1 Ensembl:ENSG00000185591 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53414964..53415063 26863196 MeRIP-seq:(Medium) rs1269304515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11974858,Human_RBP_ID_18261542,Human_RBP_ID_27630528 Human_miRNA_ID_216139,Human_miRNA_ID_660423,Human_miRNA_ID_666614,Human_miRNA_ID_672254,Human_miRNA_ID_2022196,Human_miRNA_ID_2260738,Human_miRNA_ID_2263783,Human_miRNA_ID_2266852 RMVar_hsa_circ_108173,RMVar_hsa_circ_156935 90702 RMVar_ID_90702 Human_SNP_ID_501612814 m1A Human chr12 - 53416055 53416054 53416055 CAGTGTTAAGAGAGAAATAAACTTGGGTTTTTAGGCACCAGAGATTGGAGCACCACCCATCCCTT CAGTGTTAAGAGAGAAATAAACTTGGGTTTTT_GGCACCAGAGATTGGAGCACCACCCATCCCTT CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53415951..53416075 32194978 MeRIP-seq:(Medium) rs1157853051 Functional Loss DEL dbSNP153 33..33 33 - - - 90703 RMVar_ID_90703 Human_SNP_ID_501623226 m1A Human chr12 + 53452300 53452300 53452300 GCGGGGCCCCCCTCGCCTTCCCGCCCGCCCCTATTGTTCCGCCCCCGGCCTCCCGCCCTTCCCCT GCGGGGCCCCCCTCGCCTTCCCGCCCGCCCCTGTTGTTCCGCCCCCGGCCTCCCGCCCTTCCCCT A G PCBP2,AC023509.1 Ensembl:ENSG00000197111,Ensembl:ENSG00000257379 Protein coding,lincRNA 5'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:53452101..53452425 26863410 MeRIP-seq:(Medium) rs1246138112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228305,Human_RBP_ID_422347,Human_RBP_ID_3418958,Human_RBP_ID_4256455,Human_RBP_ID_5087498,Human_RBP_ID_5094274,Human_RBP_ID_5126872,Human_RBP_ID_5536081,Human_RBP_ID_5645361,Human_RBP_ID_17074840,Human_RBP_ID_17471994,Human_RBP_ID_17560868,Human_RBP_ID_18434370,Human_RBP_ID_18934488,Human_RBP_ID_22532423,Human_RBP_ID_23564717,Human_RBP_ID_24979402,Human_RBP_ID_26423755,Human_RBP_ID_26907930 Human_Splice_Rec_1375379,Human_Splice_Rec_1375405,Human_Splice_Rec_1375429,Human_Splice_Rec_1375453,Human_Splice_Rec_1375481,Human_Splice_Rec_1375503,Human_Splice_Rec_1375529,Human_Splice_Rec_1375539 Human_miRNA_ID_2386931,Human_miRNA_ID_2388406,Human_miRNA_ID_2399556,Human_miRNA_ID_3030610 RMVar_hsa_circ_82729,RMVar_hsa_circ_156946 90704 RMVar_ID_90704 Human_SNP_ID_501623244 m1A Human chr12 - 53452351 53452351 53452351 GGCTTACCTGCAGGCGCGAGGCGACTGAGGGGAAAAGGGGAGCGGGCGGGAAGGGGAAGGGCGGG GGCTTACCTGCAGGCGCGAGGCGACTGAGGGGCAAAGGGGAGCGGGCGGGAAGGGGAAGGGCGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:53452101..53452454 26863196 MeRIP-seq:(Medium) rs1282147786 Functional Loss SNV dbSNP153 33..33 33 - - - 90705 RMVar_ID_90705 Human_SNP_ID_501624103 m1A Human chr12 + 53454654 53454654 53454654 TAAGGAAAAGTGTAAAGTAGAAAATATTGATAAGGTGAAAATAACTTGGGAAATAATAACCTTGT TAAGGAAAAGTGTAAAGTAGAAAATATTGATAGGGTGAAAATAACTTGGGAAATAATAACCTTGT A G PCBP2,AC023509.1 Ensembl:ENSG00000197111,Ensembl:ENSG00000257379 Protein coding,lincRNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:53454652..53454775 26863410 MeRIP-seq:(Medium) rs1357305549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1167315,Human_RBP_ID_1473532,Human_RBP_ID_1796962,Human_RBP_ID_11975236,Human_RBP_ID_17601405,Human_RBP_ID_22905225 RMVar_hsa_circ_82729,RMVar_hsa_circ_156946 90706 RMVar_ID_90706 Human_SNP_ID_501624125 m1A Human chr12 - 53454736 53454736 53454736 GTGGTCAAGTCTTTGGTCACTGGTTGGGGGTGAAAGCCAAAAACTAAAATGCAAACATGACCAAA GTGGTCAAGTCTTTGGTCACTGGTTGGGGGTGCAAGCCAAAAACTAAAATGCAAACATGACCAAA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:53454726..53454750;chr12:53454726..53454775 26863196 MeRIP-seq:(Medium) rs1224766397 Functional Loss SNV dbSNP153 33..33 33 - - - 90707 RMVar_ID_90707 Human_SNP_ID_501629682 m1A Human chr12 + 53471593 53471593 53471593 GGGGTGGGGGGGTGGGATTCTTAGACCTAGCCATGCAACTCTAATTCGGTGTGCCTTGTTTTTCT GGGGTGGGGGGGTGGGATTCTTAGACCTAGCCGTGCAACTCTAATTCGGTGTGCCTTGTTTTTCT A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53471589..53471745 26863196 MeRIP-seq:(Medium) rs773553985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5347361,Human_RBP_ID_22644866,Human_RBP_ID_22736678,Human_RBP_ID_23158219,Human_RBP_ID_26777318 RMVar_hsa_circ_36422,RMVar_hsa_circ_274363,RMVar_hsa_circ_156952,RMVar_hsa_circ_360596,RMVar_hsa_circ_322017,RMVar_hsa_circ_156959,RMVar_hsa_circ_118133,RMVar_hsa_circ_127496,RMVar_hsa_circ_156967,RMVar_hsa_circ_156968,RMVar_hsa_circ_295336,RMVar_hsa_circ_116979,RMVar_hsa_circ_156971,RMVar_hsa_circ_276149,RMVar_hsa_circ_156973,RMVar_hsa_circ_156974,RMVar_hsa_circ_156976,RMVar_hsa_circ_338631 90708 RMVar_ID_90708 Human_SNP_ID_501630740 m1A Human chr12 + 53474975 53474972 53474975 AACCCTCCACCCCTTCTTCTTCTTCCTCCTCCACCACCACCCCCTCGCTCGCCACAGCGGGGACC AACCCTCCACCCCTTCTTCTTCTTCCTCCT___CCACCACCCCCTCGCTCGCCACAGCGGGGACC TCCA T PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53474935..53475135 32194978 MeRIP-seq:(Medium) rs1565873661 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_18934498,Human_RBP_ID_19828406,Human_RBP_ID_21918831,Human_RBP_ID_22794481,Human_RBP_ID_23564846,Human_RBP_ID_27423052 RMVar_hsa_circ_127496,RMVar_hsa_circ_156968 90709 RMVar_ID_90709 Human_SNP_ID_501630743 m1A Human chr12 + 53474978 53474978 53474978 CCTCCACCCCTTCTTCTTCTTCCTCCTCCACCACCACCCCCTCGCTCGCCACAGCGGGGACCTCC CCTCCACCCCTTCTTCTTCTTCCTCCTCCACCGCCACCCCCTCGCTCGCCACAGCGGGGACCTCC A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53474927..53475106 26863196 MeRIP-seq:(Medium) rs1312818286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18934498,Human_RBP_ID_21918831,Human_RBP_ID_23564846,Human_RBP_ID_27423052 RMVar_hsa_circ_127496,RMVar_hsa_circ_156968 90710 RMVar_ID_90710 Human_SNP_ID_501630762 m1A Human chr12 + 53475012 53475012 53475012 CACCCCCTCGCTCGCCACAGCGGGGACCTCCGACGCACCCTCCAGCCTCCCCAACCCTCTTCCGA CACCCCCTCGCTCGCCACAGCGGGGACCTCCGGCGCACCCTCCAGCCTCCCCAACCCTCTTCCGA A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53474879..53475112 26863196 MeRIP-seq:(Medium) rs770410083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22574585 RMVar_hsa_circ_127496,RMVar_hsa_circ_156968 90711 RMVar_ID_90711 Human_SNP_ID_501632180 m1A Human chr12 + 53479461 53479461 53479461 TGGGGAGCAGCTAGAACAATGCAGATTCATCCATAATCCCTTTCTGCTGTTCACCACCACCCATG TGGGGAGCAGCTAGAACAATGCAGATTCATCCGTAATCCCTTTCTGCTGTTCACCACCACCCATG A G PCBP2 Ensembl:ENSG00000197111 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53479401..53479617 32194978 MeRIP-seq:(Medium) rs772280779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36031,Human_RBP_ID_296176,Human_RBP_ID_422421,Human_RBP_ID_1269698,Human_RBP_ID_1473650,Human_RBP_ID_1797075,Human_RBP_ID_3408441,Human_RBP_ID_4256494,Human_RBP_ID_5491666,Human_RBP_ID_6197115,Human_RBP_ID_8068532,Human_RBP_ID_8247721,Human_RBP_ID_8378871,Human_RBP_ID_8783014,Human_RBP_ID_9018330,Human_RBP_ID_9278195,Human_RBP_ID_11976646,Human_RBP_ID_17239170,Human_RBP_ID_17354889,Human_RBP_ID_17472019,Human_RBP_ID_17684732,Human_RBP_ID_17821843,Human_RBP_ID_18206364,Human_RBP_ID_18261578,Human_RBP_ID_22437094,Human_RBP_ID_23270101,Human_RBP_ID_26417421,Human_RBP_ID_26908000,Human_RBP_ID_27423054,Human_RBP_ID_27558079 Human_Splice_Rec_1375404,Human_Splice_Rec_1375428,Human_Splice_Rec_1375452,Human_Splice_Rec_1375480,Human_Splice_Rec_1375502,Human_Splice_Rec_1375528,Human_Splice_Rec_1375566,Human_Splice_Rec_1375610,Human_Splice_Rec_1375636,Human_Splice_Rec_1375660,Human_Splice_Rec_1375682,Human_Splice_Rec_1375720,Human_Splice_Rec_1375742,Human_Splice_Rec_1375774,Human_Splice_Rec_1375782,Human_Splice_Rec_1375786 RMVar_hsa_circ_127496,RMVar_hsa_circ_156968 90712 RMVar_ID_90712 Human_SNP_ID_501632637 m1A Human chr12 - 53480812 53480812 53480812 GGCGGTGGGAGGGGCAGGAGAGAAAACCACTTAGACTGCACTTTTCTGTTCCGTTTACTCTGTTT GGCGGTGGGAGGGGCAGGAGAGAAAACCACTTGGACTGCACTTTTCTGTTCCGTTTACTCTGTTT T C MAP3K12 Ensembl:ENSG00000139625 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53480762..53480863 32194978 MeRIP-seq:(Medium) rs1017202245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1942770,Human_miRNA_ID_1945816,Human_miRNA_ID_2116961,Human_miRNA_ID_2149572,Human_miRNA_ID_2200539,Human_miRNA_ID_2203603,Human_miRNA_ID_2806059,Human_miRNA_ID_2809202,Human_miRNA_ID_2812344,Human_miRNA_ID_2816064,Human_miRNA_ID_2863327,Human_miRNA_ID_3113056 RMVar_hsa_circ_109557,RMVar_hsa_circ_156977 90713 RMVar_ID_90713 Human_SNP_ID_501638594 m1A Human chr12 + 53501408 53501408 53501408 GTCACGGTGGCGCCCGCGGGGACGGAGGAGGGAATGAGTGAAGAGGAGCAAGGCTCCGGCACTAC GTCACGGTGGCGCCCGCGGGGACGGAGGAGGGGATGAGTGAAGAGGAGCAAGGCTCCGGCACTAC A G TARBP2 Ensembl:ENSG00000139546 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53501119..53501599 26863196 MeRIP-seq:(Medium) rs746347538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4229037,Human_RBP_ID_6197317,Human_RBP_ID_8940711,Human_RBP_ID_26322899 Human_Splice_Rec_1375919,Human_Splice_Rec_1375951,Human_Splice_Rec_1375961,Human_Splice_Rec_1375977,Human_Splice_Rec_1375983,Human_Splice_Rec_1375985,Human_Splice_Rec_1376001,Human_Splice_Rec_1376003,Human_Splice_Rec_1376007 90714 RMVar_ID_90714 Human_SNP_ID_501639046 m1A Human chr12 + 53503101 53503101 53503101 AGGTGGCCCTCAAACACCTCAAAGGGGGGAGCATGCTGGAGCCGGCCCTGGAGGACAGCAGGTGA AGGTGGCCCTCAAACACCTCAAAGGGGGGAGCGTGCTGGAGCCGGCCCTGGAGGACAGCAGGTGA A G TARBP2 Ensembl:ENSG00000139546 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53503050..53503174 26863196 MeRIP-seq:(Medium) rs1289122609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229612,Human_RBP_ID_18975689,Human_RBP_ID_21885213,Human_RBP_ID_23305954 Human_Splice_Rec_1375922,Human_Splice_Rec_1375923,Human_Splice_Rec_1375938,Human_Splice_Rec_1375939,Human_Splice_Rec_1375964,Human_Splice_Rec_1375965,Human_Splice_Rec_1375980,Human_Splice_Rec_1375981,Human_Splice_Rec_1375988,Human_Splice_Rec_1376002,Human_Splice_Rec_1376006,Human_Splice_Rec_1376008,Human_Splice_Rec_1376009,Human_Splice_Rec_1376022,Human_Splice_Rec_1376023,Human_Splice_Rec_1376034,Human_Splice_Rec_1376035,Human_Splice_Rec_1376048,Human_Splice_Rec_1376054,Human_Splice_Rec_1376055,Human_Splice_Rec_1376070,Human_Splice_Rec_1376086,Human_Splice_Rec_1376087,Human_Splice_Rec_1376100,Human_Splice_Rec_1376101,Human_Splice_Rec_1376111 Human_miRNA_ID_969621,Human_miRNA_ID_1193756 90715 RMVar_ID_90715 Human_SNP_ID_501639627 m1A Human chr12 - 53505156 53505156 53505156 GCAGCATTTTGGCCGCCGCATTCCGCTTTGCCAATTTTTTGGAAGTGCCACTCCCTGCATGTGGA GCAGCATTTTGGCCGCCGCATTCCGCTTTGCCGATTTTTTGGAAGTGCCACTCCCTGCATGTGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53504788..53505258 32194978 MeRIP-seq:(Medium) rs1263471950 Functional Loss SNV dbSNP153 33..33 33 - - - 90716 RMVar_ID_90716 Human_SNP_ID_501639674 m1A Human chr12 - 53505257 53505257 53505257 GGTGCCCGGCCCACATGAGCCACTCACAATGGAGAAGTGGTCATCATCAGGCTCCACCTCATTGC GGTGCCCGGCCCACATGAGCCACTCACAATGGCGAAGTGGTCATCATCAGGCTCCACCTCATTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:53505207..53505694 32194978 MeRIP-seq:(Medium) rs780275010 Functional Loss SNV dbSNP153 33..33 33 - - - 90717 RMVar_ID_90717 Human_SNP_ID_501639978 m1A Human chr12 - 53506181 53506181 53506181 ACATGAGCCCAGAGGCAGAAAGAGCAGGGAGCAAAGGGTGCACATCCATGAGTCCAGCTGGGGCT ACATGAGCCCAGAGGCAGAAAGAGCAGGGAGCGAAGGGTGCACATCCATGAGTCCAGCTGGGGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53506131..53506381 32194978 MeRIP-seq:(Medium) rs1462439135 Functional Loss SNV dbSNP153 33..33 33 - - - 90718 RMVar_ID_90718 Human_SNP_ID_501667206 m1A Human chr12 + 53626326 53626326 53626326 TTGCCTCCCGCCTGCCCGCGCTCGGTCCTACAATCTGTCTCCAGCTCCTCCTTTCCCCCCTTGGC TTGCCTCCCGCCTGCCCGCGCTCGGTCCTACAGTCTGTCTCCAGCTCCTCCTTTCCCCCCTTGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53626232..53626375 26863196 MeRIP-seq:(Medium) rs765065930 Functional Loss SNV dbSNP153 33..33 33 - - - 90719 RMVar_ID_90719 Human_SNP_ID_501676767 m1A Human chr12 + 53665297 53665297 53665297 ACGGGGCCAACCAGACGCGGGAGAACTATGGGAGGTGGAGACGGCTCCTTCACATGGCAAAGAGG ACGGGGCCAACCAGACGCGGGAGAACTATGGGCGGTGGAGACGGCTCCTTCACATGGCAAAGAGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53665248..53665374 26863196 MeRIP-seq:(Medium) rs773493134 Functional Loss SNV dbSNP153 33..33 33 - - - 90720 RMVar_ID_90720 Human_SNP_ID_501678898 m1A Human chr12 + 53672619 53672619 53672619 TGGAGACAAACTTGGAGCAGGCGAACATTTTCAGGGGGTGAGGAGCTGTGGCAGGAGAGCTGGAA TGGAGACAAACTTGGAGCAGGCGAACATTTTCGGGGGGTGAGGAGCTGTGGCAGGAGAGCTGGAA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:53672576..53672675 26863410 MeRIP-seq:(Medium) rs868621545 Functional Loss SNV dbSNP153 33..33 33 - - - 90721 RMVar_ID_90721 Human_SNP_ID_501678910 m1A Human chr12 - 53672633 53672633 53672633 TACTGCTTCTGTAATTCCAGCTCTCCTGCCACAGCTCCTCACCCCCTGAAAATGTTCGCCTGCTC TACTGCTTCTGTAATTCCAGCTCTCCTGCCACTGCTCCTCACCCCCTGAAAATGTTCGCCTGCTC T A ATP5MC2 Ensembl:ENSG00000135390 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53672514..53672688 26863196 MeRIP-seq:(Medium) rs745449662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229939,Human_RBP_ID_422554,Human_RBP_ID_755675,Human_RBP_ID_810407,Human_RBP_ID_1357893,Human_RBP_ID_4246110,Human_RBP_ID_5417113,Human_RBP_ID_8783020,Human_RBP_ID_9322529,Human_RBP_ID_17357102,Human_RBP_ID_17474776,Human_RBP_ID_17650379,Human_RBP_ID_18629006,Human_RBP_ID_22435907,Human_RBP_ID_22756318,Human_RBP_ID_23565091,Human_RBP_ID_27423086 Human_Splice_Rec_1376288,Human_Splice_Rec_1376289,Human_Splice_Rec_1376296,Human_Splice_Rec_1376297,Human_Splice_Rec_1376303,Human_Splice_Rec_1376311,Human_Splice_Rec_1376318,Human_Splice_Rec_1376319,Human_Splice_Rec_1376326,Human_Splice_Rec_1376327,Human_Splice_Rec_1376334,Human_Splice_Rec_1376335 Human_miRNA_ID_2292284,Human_miRNA_ID_2357629,Human_miRNA_ID_3060068 RMVar_hsa_circ_303241,RMVar_hsa_circ_157000,RMVar_hsa_circ_372062,RMVar_hsa_circ_157002,RMVar_hsa_circ_157003,RMVar_hsa_circ_81171 90722 RMVar_ID_90722 Human_SNP_ID_501678912 m1A Human chr12 - 53672635 53672635 53672635 AATACTGCTTCTGTAATTCCAGCTCTCCTGCCACAGCTCCTCACCCCCTGAAAATGTTCGCCTGC AATACTGCTTCTGTAATTCCAGCTCTCCTGCCGCAGCTCCTCACCCCCTGAAAATGTTCGCCTGC T C ATP5MC2 Ensembl:ENSG00000135390 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:53672509..53672700 26863410 MeRIP-seq:(Medium) rs769277990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229939,Human_RBP_ID_422554,Human_RBP_ID_755675,Human_RBP_ID_810407,Human_RBP_ID_1357893,Human_RBP_ID_4246110,Human_RBP_ID_5417113,Human_RBP_ID_8783020,Human_RBP_ID_9322529,Human_RBP_ID_17357103,Human_RBP_ID_17474776,Human_RBP_ID_17650379,Human_RBP_ID_22435907,Human_RBP_ID_22756318,Human_RBP_ID_27423086 Human_Splice_Rec_1376288,Human_Splice_Rec_1376289,Human_Splice_Rec_1376296,Human_Splice_Rec_1376297,Human_Splice_Rec_1376303,Human_Splice_Rec_1376311,Human_Splice_Rec_1376318,Human_Splice_Rec_1376319,Human_Splice_Rec_1376326,Human_Splice_Rec_1376327,Human_Splice_Rec_1376334,Human_Splice_Rec_1376335 Human_miRNA_ID_2292284,Human_miRNA_ID_2357629,Human_miRNA_ID_3060068 RMVar_hsa_circ_303241,RMVar_hsa_circ_157000,RMVar_hsa_circ_372062,RMVar_hsa_circ_157002,RMVar_hsa_circ_157003,RMVar_hsa_circ_81171 90723 RMVar_ID_90723 Human_SNP_ID_501678916 m1A Human chr12 + 53672644 53672644 53672644 CATTTTCAGGGGGTGAGGAGCTGTGGCAGGAGAGCTGGAATTACAGAAGCAGTATTGTAAACGCT CATTTTCAGGGGGTGAGGAGCTGTGGCAGGAGGGCTGGAATTACAGAAGCAGTATTGTAAACGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:53672601..53672650 26863196 MeRIP-seq:(Medium) rs762522443 Functional Loss SNV dbSNP153 33..33 33 - - - 90724 RMVar_ID_90724 Human_SNP_ID_501689212 m1A Human chr12 - 53712282 53712282 53712282 AGGACATGGGGAACTGGAAAAATAAGCCTTCCAGGATTGTGGGGAGAAAGACGCTGTGGGAGAGG AGGACATGGGGAACTGGAAAAATAAGCCTTCCGGGATTGTGGGGAGAAAGACGCTGTGGGAGAGG T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53712262..53712456 26863196 MeRIP-seq:(Medium) rs1299945316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18261639 90725 RMVar_ID_90725 Human_SNP_ID_501689411 m1A Human chr12 - 53713054 53713054 53713054 GCAAGGCCAGGAGGGAGGTGGGAGGAGGTCAGAGGGAAAGGGCATCTGTGTGGACAGTCACCAGG GCAAGGCCAGGAGGGAGGTGGGAGGAGGTCAGTGGGAAAGGGCATCTGTGTGGACAGTCACCAGG T A CALCOCO1 Ensembl:ENSG00000012822 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53712905..53713115 26863196 MeRIP-seq:(Medium) rs1381805585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755352,Human_RBP_ID_810001,Human_RBP_ID_5347369,Human_RBP_ID_19056270,Human_RBP_ID_22353820,Human_RBP_ID_22414740,Human_RBP_ID_24557728,Human_RBP_ID_26322903 90726 RMVar_ID_90726 Human_SNP_ID_501689647 m1A Human chr12 - 53713875 53713875 53713875 CCTACAGGCTGCCCGGCAGCTCTGACAGACTCAGAGGACGAGTCCCCAGAAGACATGAGGCTCCC CCTACAGGCTGCCCGGCAGCTCTGACAGACTCGGAGGACGAGTCCCCAGAAGACATGAGGCTCCC T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:53713826..53714200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_22647409,Human_RBP_ID_24557729,Human_RBP_ID_25015548 Human_Splice_Rec_1376366,Human_Splice_Rec_1376394,Human_Splice_Rec_1376402,Human_Splice_Rec_1376430,Human_Splice_Rec_1376458 RMVar_hsa_circ_157004,RMVar_hsa_circ_291763 90727 RMVar_ID_90727 Human_SNP_ID_501689757 m1A Human chr12 + 53714181 53714181 53714181 CTCCTCATCCTCTGTGGTGGCATCCTCATTCCACTTCTCATCTGCCACCTTCTCCAGGCGGGCCT CTCCTCATCCTCTGTGGTGGCATCCTCATTCCTCTTCTCATCTGCCACCTTCTCCAGGCGGGCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53714084..53714284 26863196 MeRIP-seq:(Medium) rs763807375 Functional Loss SNV dbSNP153 33..33 33 - - - 90728 RMVar_ID_90728 Human_SNP_ID_501689891 m1A Human chr12 - 53714674 53714674 53714674 CCTCTTCCCTCAGGTACAGTTGTCAGAAAGTAAGCGGGAGCTGACAGAGCTGCGGTCAGCCCTGC CCTCTTCCCTCAGGTACAGTTGTCAGAAAGTACGCGGGAGCTGACAGAGCTGCGGTCAGCCCTGC T G CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53714543..53714700 26863196 MeRIP-seq:(Medium) rs200408324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942999,Human_RBP_ID_8229879,Human_RBP_ID_26321466 Human_Splice_Rec_1376362,Human_Splice_Rec_1376363,Human_Splice_Rec_1376390,Human_Splice_Rec_1376391,Human_Splice_Rec_1376399,Human_Splice_Rec_1376426,Human_Splice_Rec_1376427,Human_Splice_Rec_1376454,Human_Splice_Rec_1376455,Human_Splice_Rec_1376480,Human_Splice_Rec_1376481,Human_Splice_Rec_1376488,Human_Splice_Rec_1376489 90729 RMVar_ID_90729 Human_SNP_ID_501690195 m1A Human chr12 + 53715744 53715744 53715744 GAGGGTCTGACCACATGTAGGAGTCCCCACAGAGGTGGGGGCAGTGGCCATCAGATTGCCAGGTA GAGGGTCTGACCACATGTAGGAGTCCCCACAGCGGTGGGGGCAGTGGCCATCAGATTGCCAGGTA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53715741..53715975 26863196 MeRIP-seq:(Medium) rs747968881 Functional Loss SNV dbSNP153 33..33 33 - - - 90730 RMVar_ID_90730 Human_SNP_ID_501690238 m1A Human chr12 - 53715844 53715844 53715844 AGGCTGGCTGAGCTCGGTTTGCACTTGAAGGAAGAAAAATGCCAATGGAGCAAGGAGCGGGCAGG AGGCTGGCTGAGCTCGGTTTGCACTTGAAGGAGGAAAAATGCCAATGGAGCAAGGAGCGGGCAGG T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53715775..53716003 26863196 MeRIP-seq:(Medium) rs1175977607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18977244 Human_Splice_Rec_1376359,Human_Splice_Rec_1376387,Human_Splice_Rec_1376423,Human_Splice_Rec_1376451,Human_Splice_Rec_1376477,Human_Splice_Rec_1376485 90731 RMVar_ID_90731 Human_SNP_ID_501691200 m1A Human chr12 - 53719769 53719769 53719769 CGGGAACAAGAGAAGCTCCTTGGGCAACTGAAAGAAGTACAAGCAGACAAGGAGCAAAGTGAGGT CGGGAACAAGAGAAGCTCCTTGGGCAACTGAAGGAAGTACAAGCAGACAAGGAGCAAAGTGAGGT T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53719751..53719825 26863196 MeRIP-seq:(Medium) rs1467359323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874626,Human_RBP_ID_27806639 Human_Splice_Rec_1376354,Human_Splice_Rec_1376355,Human_Splice_Rec_1376382,Human_Splice_Rec_1376383,Human_Splice_Rec_1376420,Human_Splice_Rec_1376421,Human_Splice_Rec_1376446,Human_Splice_Rec_1376447,Human_Splice_Rec_1376472,Human_Splice_Rec_1376473,Human_Splice_Rec_1376491,Human_Splice_Rec_1376504 RMVar_hsa_circ_23912,RMVar_hsa_circ_277548,RMVar_hsa_circ_157005 90732 RMVar_ID_90732 Human_SNP_ID_501691212 m1A Human chr12 + 53719802 53719802 53719802 TTCAGTTGCCCAAGGAGCTTCTCTTGTTCCCGAGTCAGGGCCTTCACTGTGTCTCTAAGCCTGTG TTCAGTTGCCCAAGGAGCTTCTCTTGTTCCCGTGTCAGGGCCTTCACTGTGTCTCTAAGCCTGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53719700..53719875;chr12:53719737..53719884 26863196 MeRIP-seq:(Medium) rs1298801962 Functional Loss SNV dbSNP153 33..33 33 - - - 90733 RMVar_ID_90733 Human_SNP_ID_501742811 m1A Human chr12 + 53936898 53936898 53936898 CTTGGCCAGGCCCTGTTTGCTCTCCTCGTTTTACCTTGACCTTGGACTCCAGCAGCAGGATAAGC CTTGGCCAGGCCCTGTTTGCTCTCCTCGTTTTGCCTTGACCTTGGACTCCAGCAGCAGGATAAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53936876..53937124 26863196 MeRIP-seq:(Medium) rs910146323 Functional Loss SNV dbSNP153 33..33 33 - - - 90734 RMVar_ID_90734 Human_SNP_ID_501743357 m1A Human chr12 + 53938944 53938944 53938944 GACTTCGCTGCTCCTGCATCCACGCTGGCCGGAGAGCCTTATGTACGTCTATGAGGACAGCGCGG GACTTCGCTGCTCCTGCATCCACGCTGGCCGGCGAGCCTTATGTACGTCTATGAGGACAGCGCGG A C HOXC13 Ensembl:ENSG00000123364 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53938776..53939402 26863196 MeRIP-seq:(Medium) rs1325238516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18629021 90735 RMVar_ID_90735 Human_SNP_ID_501743432 m1A Human chr12 + 53939064 53939053 53939064 GGGGGGTGGCTGCAGCGGAGCGAGCCCCGGCAAAGCCCCGAGCATGGATGGTCTGGGCAGCAGCT GGGGGGTGGCTGCAGCGGAGCG___________AGCCCCGAGCATGGATGGTCTGGGCAGCAGCT GAGCCCCGGCAA G HOXC13 Ensembl:ENSG00000123364 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:53938958..53939177 26863196 MeRIP-seq:(Medium) rs1169109267 Functional Loss DEL dbSNP153 23..33 33 - - - 90736 RMVar_ID_90736 Human_SNP_ID_501743480 m1A Human chr12 + 53939186 53939186 53939186 CTCCCCTGGGCGCCCCTCAGGGCGCCGTCTATACGGACATCCCGGCCCCGGAGGCGGCGCGCCAG CTCCCCTGGGCGCCCCTCAGGGCGCCGTCTATGCGGACATCCCGGCCCCGGAGGCGGCGCGCCAG A G HOXC13 Ensembl:ENSG00000123364 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:53939099..53939250 26863410 MeRIP-seq:(Medium) rs767074923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4229282 90737 RMVar_ID_90737 Human_SNP_ID_501745086 m1A Human chr12 + 53945372 53945372 53945372 AGAAGAGTATTTAATGTTAAGGAAAGAGAAGAACCGCGCCGCCCGGAGGCAGAGAGGCTCCATGG AGAAGAGTATTTAATGTTAAGGAAAGAGAAGACCCGCGCCGCCCGGAGGCAGAGAGGCTCCATGG A C HOXC13 Ensembl:ENSG00000123364 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53945321..53945441 26863196 MeRIP-seq:(Medium) rs953302389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_422578,Human_RBP_ID_27423093 90738 RMVar_ID_90738 Human_SNP_ID_501750820 m1A Human chr12 - 53966292 53966292 53966292 GAGTGGGGAGTGGAGAGAGGGAGCCCAGAGTTACAGACGGCGGCGAGAGGTACAGAAGACTGGGA GAGTGGGGAGTGGAGAGAGGGAGCCCAGAGTTGCAGACGGCGGCGAGAGGTACAGAAGACTGGGA T C HOTAIR Ensembl:ENSG00000228630 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53966124..53966291 26863196 MeRIP-seq:(Medium) rs534252584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5556413,Human_RBP_ID_8248244 Human_Splice_Rec_1376646,Human_Splice_Rec_1376647,Human_Splice_Rec_1376658,Human_Splice_Rec_1376659,Human_Splice_Rec_1376664,Human_Splice_Rec_1376665,Human_Splice_Rec_1376670,Human_Splice_Rec_1376671,Human_Splice_Rec_1376678,Human_Splice_Rec_1376679 90739 RMVar_ID_90739 Human_SNP_ID_501751410 m1A Human chr12 + 53968668 53968668 53968668 TGTGGAAGCTTTCGGATCAAGCTCCAGAGCACAGGCGAGTCAGAGTTCCCCACTGCCTGCCTAGG TGTGGAAGCTTTCGGATCAAGCTCCAGAGCACGGGCGAGTCAGAGTTCCCCACTGCCTGCCTAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53968597..53968670 26863196 MeRIP-seq:(Medium) rs768878421 Functional Loss SNV dbSNP153 33..33 33 - - - 90740 RMVar_ID_90740 Human_SNP_ID_501752911 m1A Human chr12 + 53973923 53973923 53973923 TGGCCAAGGAGCCGGCCAAAGGAGCCGCCCCCAGTAGGTAGCAGCGGCCGGGGAACGGGCGGGCA TGGCCAAGGAGCCGGCCAAAGGAGCCGCCCCCCGTAGGTAGCAGCGGCCGGGGAACGGGCGGGCA A C HOXC11 Ensembl:ENSG00000123388 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53973894..53974069 26863196 MeRIP-seq:(Medium) rs1308575089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1376683,Human_Splice_Rec_1376685 RMVar_hsa_circ_110245,RMVar_hsa_circ_157008 90741 RMVar_ID_90741 Human_SNP_ID_501753268 m1A Human chr12 - 53975081 53975081 53975081 CAGCCCGCTGAGCGCTCAGCGGCCCTTCTCCTAGCCCACCGCGGGCAGCCCTCCCGCCAGGCGGC CAGCCCGCTGAGCGCTCAGCGGCCCTTCTCCTGGCCCACCGCGGGCAGCCCTCCCGCCAGGCGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53975078..53975188 26863196 MeRIP-seq:(Medium) rs1449993528 Functional Loss SNV dbSNP153 33..33 33 - - - 90742 RMVar_ID_90742 Human_SNP_ID_501756289 m1A Human chr12 + 53985240 53985240 53985240 ATGTCAGCTCCTCCGCTGTAGTATTGCTCCTTAAAAACCCCTCTCTCTGAAAATGACATGCCCTC ATGTCAGCTCCTCCGCTGTAGTATTGCTCCTTCAAAACCCCTCTCTCTGAAAATGACATGCCCTC A C HOXC10 Ensembl:ENSG00000180818 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53985190..53985349 26863196 MeRIP-seq:(Medium) rs1263235995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5417119,Human_RBP_ID_5437799 90743 RMVar_ID_90743 Human_SNP_ID_501758861 m1A Human chr12 + 53994152 53994152 53994152 CTCTCTGGGACCTCGCCCCGGCCCACGGCCTGACTTCGGCTCGGAGATGCAGCCCTTCCCGAGAA CTCTCTGGGACCTCGCCCCGGCCCACGGCCTGGCTTCGGCTCGGAGATGCAGCCCTTCCCGAGAA A G AC012531.3,HOXC6 Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53994102..53994168 26863196 MeRIP-seq:(Medium) rs1387541578 Functional Loss SNV dbSNP153 33..33 33 - - - 90744 RMVar_ID_90744 Human_SNP_ID_501760014 m1A Human chr12 - 53998225 53998225 53998225 CTCTCTGGCTCTTTCCTTTTCCTTTTTGGTCTAAGGGGGCGGCTTAACGGGGCTGGGATTTCAAC CTCTCTGGCTCTTTCCTTTTCCTTTTTGGTCTCAGGGGGCGGCTTAACGGGGCTGGGATTTCAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53998176..53998428 26863196 MeRIP-seq:(Medium) rs982952888 Functional Loss SNV dbSNP153 33..33 33 - - - 90745 RMVar_ID_90745 Human_SNP_ID_501760476 m1A Human chr12 + 53999918 53999918 53999918 CGTCCTGAGGGGGTGACCGGTGCCTTGGGTCCAGAGTTCCGGACCCCCAGGAAATCGCAGGTCGC CGTCCTGAGGGGGTGACCGGTGCCTTGGGTCCCGAGTTCCGGACCCCCAGGAAATCGCAGGTCGC A C HOXC9,AC012531.3,HOXC6 Ensembl:ENSG00000180806,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53999867..53999957 26863196 MeRIP-seq:(Medium) rs1015139347 Functional Loss SNV dbSNP153 33..33 33 - - - 90746 RMVar_ID_90746 Human_SNP_ID_501760674 m1A Human chr12 + 54000418 54000418 54000418 GGCGCCCGTGCCCTCTCAGTCGTCCGTGGTATATCACCCGTACGGCCCCCAGCCCCACCTCGGCG GGCGCCCGTGCCCTCTCAGTCGTCCGTGGTATGTCACCCGTACGGCCCCCAGCCCCACCTCGGCG A G HOXC9,AC012531.3,HOXC6 Ensembl:ENSG00000180806,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54000367..54000500 26863196 MeRIP-seq:(Medium) rs1017342906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5256719,Human_RBP_ID_18479016,Human_RBP_ID_22369819,Human_RBP_ID_22709944,Human_RBP_ID_26908184 Human_miRNA_ID_1356354 90747 RMVar_ID_90747 Human_SNP_ID_501761399 m1A Human chr12 + 54002654 54002654 54002654 GGATGAAGATGAAAAAGATGAATAAAGAGAAAACCGACAAGGAGCAGTCCTAAACCCTACCCAGC GGATGAAGATGAAAAAGATGAATAAAGAGAAACCCGACAAGGAGCAGTCCTAAACCCTACCCAGC A C HOXC9,AC012531.3,HOXC6 Ensembl:ENSG00000180806,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54002604..54002900 26863196 MeRIP-seq:(Medium) rs896220275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1473793,Human_RBP_ID_26321472 90748 RMVar_ID_90748 Human_SNP_ID_501761400 m1A Human chr12 + 54002654 54002654 54002654 GGATGAAGATGAAAAAGATGAATAAAGAGAAAACCGACAAGGAGCAGTCCTAAACCCTACCCAGC GGATGAAGATGAAAAAGATGAATAAAGAGAAAGCCGACAAGGAGCAGTCCTAAACCCTACCCAGC A G HOXC9,AC012531.3,HOXC6 Ensembl:ENSG00000180806,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54002604..54002900 26863196 MeRIP-seq:(Medium) rs896220275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1473793,Human_RBP_ID_26321472 90749 RMVar_ID_90749 Human_SNP_ID_501761841 m1A Human chr12 + 54004172 54004166 54004173 AGCTGCAGCATTTCTGGGGGATGGTGTGCCCAAGGCCCAAGGAAGCTGGCCAGAGATTAGCCAGG AGCTGCAGCATTTCTGGGGGATGGTGT_______GCCCAAGGAAGCTGGCCAGAGATTAGCCAGG TGCCCAAG T AC012531.3,HOXC6 Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54004154..54004272 26863196 MeRIP-seq:(Medium) rs539834974 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_3418353,Human_RBP_ID_5314565 90750 RMVar_ID_90750 Human_SNP_ID_501763885 m1A Human chr12 + 54011281 54011281 54011281 CCGAAGGATGAAGTGGAAAAAGGAGAACAACAAGGATAAACTGCCGGGAGCCCGAGATGAGGAGA CCGAAGGATGAAGTGGAAAAAGGAGAACAACAGGGATAAACTGCCGGGAGCCCGAGATGAGGAGA A G HOXC8,AC012531.3,HOXC6 Ensembl:ENSG00000037965,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:54011230..54011390 26863196 MeRIP-seq:(Medium) rs577774629 Functional Loss SNV dbSNP153 33..33 33 - - - 90751 RMVar_ID_90751 Human_SNP_ID_501763900 m1A Human chr12 - 54011306 54011306 54011306 TCCTCATTTCCTTCTTCCTCCACCTTCTCCTCATCTCGGGCTCCCGGCAGTTTATCCTTGTTGTT TCCTCATTTCCTTCTTCCTCCACCTTCTCCTCTTCTCGGGCTCCCGGCAGTTTATCCTTGTTGTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54011265..54011361 26863196 MeRIP-seq:(Medium) rs1277088819 Functional Loss SNV dbSNP153 33..33 33 - - - 90752 RMVar_ID_90752 Human_SNP_ID_501765878 m1A Human chr12 + 54017357 54017353 54017357 TCGGCAGCGGCACAGAATGAGGGAAGACGAGAAAGAGAGTGGGAGAGAGAGAGGCAGAGAGGGAG TCGGCAGCGGCACAGAATGAGGGAAGACG____AGAGAGTGGGAGAGAGAGAGGCAGAGAGGGAG GAGAA G AC012531.2,HOXC4,AC012531.3,HOXC6 Ensembl:ENSG00000273046,Ensembl:ENSG00000198353,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 lincRNA,Protein coding,Protein coding,Protein coding exon,5'UTR,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54017270..54017858 26863196 MeRIP-seq:(Medium) rs1372142054 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5246449 Human_Splice_Rec_1376713,Human_Splice_Rec_1376737,Human_Splice_Rec_1376747 Human_miRNA_ID_340370,Human_miRNA_ID_340371,Human_miRNA_ID_1692770,Human_miRNA_ID_1692771,Human_miRNA_ID_3201249 90753 RMVar_ID_90753 Human_SNP_ID_501765879 m1A Human chr12 + 54017358 54017357 54017359 CGGCAGCGGCACAGAATGAGGGAAGACGAGAAAGAGAGTGGGAGAGAGAGAGGCAGAGAGGGAGA CGGCAGCGGCACAGAATGAGGGAAGACGAGAA__AGAGTGGGAGAGAGAGAGGCAGAGAGGGAGA AAG A AC012531.2,HOXC4,AC012531.3,HOXC6 Ensembl:ENSG00000273046,Ensembl:ENSG00000198353,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 lincRNA,Protein coding,Protein coding,Protein coding exon,5'UTR,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:54017258..54034320 26863196 MeRIP-seq:(Medium) rs1370769959 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5246449 Human_Splice_Rec_1376713,Human_Splice_Rec_1376737,Human_Splice_Rec_1376747 Human_miRNA_ID_340370,Human_miRNA_ID_340371,Human_miRNA_ID_1692770,Human_miRNA_ID_1692771,Human_miRNA_ID_3201249 90754 RMVar_ID_90754 Human_SNP_ID_501765894 m1A Human chr12 + 54017402 54017401 54017402 AGAGAGAGGCAGAGAGGGAGAGAGGGAGAGTGACAGCAGCGCTCGGTAAGTGTTTCCTTATTGGT AGAGAGAGGCAGAGAGGGAGAGAGGGAGAGTG_CAGCAGCGCTCGGTAAGTGTTTCCTTATTGGT GA G AC012531.2,HOXC4,AC012531.3,HOXC6 Ensembl:ENSG00000273046,Ensembl:ENSG00000198353,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 lincRNA,Protein coding,Protein coding,Protein coding exon,5'UTR,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:54017354..54017501 26863196 MeRIP-seq:(Medium) rs1056674160 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5246449 Human_Splice_Rec_1376713,Human_Splice_Rec_1376737,Human_Splice_Rec_1376747 Human_miRNA_ID_3208743 90755 RMVar_ID_90755 Human_SNP_ID_501765895 m1A Human chr12 + 54017402 54017402 54017402 AGAGAGAGGCAGAGAGGGAGAGAGGGAGAGTGACAGCAGCGCTCGGTAAGTGTTTCCTTATTGGT AGAGAGAGGCAGAGAGGGAGAGAGGGAGAGTGGCAGCAGCGCTCGGTAAGTGTTTCCTTATTGGT A G AC012531.2,HOXC4,AC012531.3,HOXC6 Ensembl:ENSG00000273046,Ensembl:ENSG00000198353,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 lincRNA,Protein coding,Protein coding,Protein coding exon,5'UTR,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:54017354..54017501 26863196 MeRIP-seq:(Medium) rs1449758321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246449 Human_Splice_Rec_1376713,Human_Splice_Rec_1376737,Human_Splice_Rec_1376747 Human_miRNA_ID_3208743 90756 RMVar_ID_90756 Human_SNP_ID_501771995 m1A Human chr12 + 54039243 54039235 54039243 GGAGCATGCCTGGGGAGCAGCGGTGTCTGGGCATCTGCTTTGTGGAGAGGTGCTGTTGGGGGATG GGAGCATGCCTGGGGAGCAGCGGTG________TCTGCTTTGTGGAGAGGTGCTGTTGGGGGATG GTCTGGGCA G HOXC4 Ensembl:ENSG00000198353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54039237..54039304 26863196 MeRIP-seq:(Medium) rs569416055 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_23565323 90757 RMVar_ID_90757 Human_SNP_ID_501771998 m1A Human chr12 + 54039243 54039243 54039243 GGAGCATGCCTGGGGAGCAGCGGTGTCTGGGCATCTGCTTTGTGGAGAGGTGCTGTTGGGGGATG GGAGCATGCCTGGGGAGCAGCGGTGTCTGGGCTTCTGCTTTGTGGAGAGGTGCTGTTGGGGGATG A T HOXC4 Ensembl:ENSG00000198353 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54039237..54039304 26863196 MeRIP-seq:(Medium) rs1020831791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23565323 90758 RMVar_ID_90758 Human_SNP_ID_501775806 m1A Human chr12 - 54054232 54054232 54054232 CGGGGCTGGGGACGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCGGCTCGCAGAGCGACTGTGATT CGGGGCTGGGGACGGGGAGGCGGAGGCGCCTGGGAGAGGCGCCGGCTCGCAGAGCGACTGTGATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:54054181..54054281 26863196 MeRIP-seq:(Medium) rs1239605514 Functional Loss SNV dbSNP153 33..33 33 - - - 90759 RMVar_ID_90759 Human_SNP_ID_501775819 m1A Human chr12 - 54054253 54054252 54054253 GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGGACGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGG_CGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54054204..54054353 26863196 MeRIP-seq:(Medium) rs1555187450 Functional Loss DEL dbSNP153 33..33 33 - - - 90760 RMVar_ID_90760 Human_SNP_ID_501775820 m1A Human chr12 - 54054253 54054253 54054253 GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGGACGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGGGCGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54054204..54054353 26863196 MeRIP-seq:(Medium) rs967730434 Functional Loss SNV dbSNP153 33..33 33 - - - 90761 RMVar_ID_90761 Human_SNP_ID_501793689 m1A Human chr12 - 54126369 54126369 54126369 GAGAGCATTCAGGCGCCCGGGCTGGGGGCTACACTGCTGGCGCGGGATGGCCCAGGACAGAGTGG GAGAGCATTCAGGCGCCCGGGCTGGGGGCTACGCTGCTGGCGCGGGATGGCCCAGGACAGAGTGG T C SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:54126276..54126484 26863410 MeRIP-seq:(Medium) rs886516424 Functional Loss SNV dbSNP153 33..33 33 - - - 90762 RMVar_ID_90762 Human_SNP_ID_501801264 m1A Human chr12 - 54158680 54158677 54158680 GGGTTGGGTGACACTGAACTGGACGCTTGAGGAGGTTGTGACACATCAGTGTGGGAGGCTCCAGG GGGTTGGGTGACACTGAACTGGACGCTTGAGG___TTGTGACACATCAGTGTGGGAGGCTCCAGG ACCT A SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54158661..54158732 26863196 MeRIP-seq:(Medium) rs1390563960 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_23565531 90763 RMVar_ID_90763 Human_SNP_ID_501801919 m1A Human chr12 - 54161565 54161565 54161565 AAGAACAGTGGGAGAAGTGGAGAGAGAAGCAGAGGCTGGGGAGATGGGAAAGAGTACAAGAGGAG AAGAACAGTGGGAGAAGTGGAGAGAGAAGCAGGGGCTGGGGAGATGGGAAAGAGTACAAGAGGAG T C SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54161559..54161703 26863196 MeRIP-seq:(Medium) rs1180665579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3314 90764 RMVar_ID_90764 Human_SNP_ID_501806840 m1A Human chr12 - 54183521 54183521 54183521 GTAGGTCCTCCCGCCCCATTCTGTCTCAACACATATACTGGCTCCTGTGGTCCGAGGCCCTCTCC GTAGGTCCTCCCGCCCCATTCTGTCTCAACACGTATACTGGCTCCTGTGGTCCGAGGCCCTCTCC T C SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54183519..54183634 26863196 MeRIP-seq:(Medium) rs750363369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17186234 RMVar_hsa_circ_352229,RMVar_hsa_circ_66280,RMVar_hsa_circ_104034,RMVar_hsa_circ_276429,RMVar_hsa_circ_157009,RMVar_hsa_circ_330801 90765 RMVar_ID_90765 Human_SNP_ID_501806841 m1A Human chr12 - 54183521 54183521 54183521 GTAGGTCCTCCCGCCCCATTCTGTCTCAACACATATACTGGCTCCTGTGGTCCGAGGCCCTCTCC GTAGGTCCTCCCGCCCCATTCTGTCTCAACACCTATACTGGCTCCTGTGGTCCGAGGCCCTCTCC T G SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54183519..54183634 26863196 MeRIP-seq:(Medium) rs750363369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17186234 RMVar_hsa_circ_352229,RMVar_hsa_circ_66280,RMVar_hsa_circ_104034,RMVar_hsa_circ_276429,RMVar_hsa_circ_157009,RMVar_hsa_circ_330801 90766 RMVar_ID_90766 Human_SNP_ID_501807009 m1A Human chr12 + 54183939 54183939 54183939 CATGGATGGACCCCAGCAGGAAAGCCTGGGGCATATGTCCATGCCGCTGTCACCTGGGAAAAGAG CATGGATGGACCCCAGCAGGAAAGCCTGGGGCGTATGTCCATGCCGCTGTCACCTGGGAAAAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54183777..54183957 26863196 MeRIP-seq:(Medium) rs747175374 Functional Loss SNV dbSNP153 33..33 33 - - - 90767 RMVar_ID_90767 Human_SNP_ID_501808432 m1A Human chr12 + 54188839 54188838 54188839 TCCCTGCACTGAGTCTTACCCCATACGGAGGGAGGGACCCCAAAATATAGAAATTCTAACCACCC TCCCTGCACTGAGTCTTACCCCATACGGAGGG_GGGACCCCAAAATATAGAAATTCTAACCACCC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54188810..54188953 26863196 MeRIP-seq:(Medium) rs1477384680 Functional Loss DEL dbSNP153 33..33 33 - - - 90768 RMVar_ID_90768 Human_SNP_ID_501808433 m1A Human chr12 + 54188839 54188839 54188839 TCCCTGCACTGAGTCTTACCCCATACGGAGGGAGGGACCCCAAAATATAGAAATTCTAACCACCC TCCCTGCACTGAGTCTTACCCCATACGGAGGGTGGGACCCCAAAATATAGAAATTCTAACCACCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54188810..54188953 26863196 MeRIP-seq:(Medium) rs1179162082 Functional Loss SNV dbSNP153 33..33 33 - - - 90769 RMVar_ID_90769 Human_SNP_ID_501819315 m1A Human chr12 + 54233067 54233067 54233067 CACCCTCTTACTACATCACATCCCTCCCCACAATACCCAGAGGGCTGCATTTTTCCAACCTTTCT CACCCTCTTACTACATCACATCCCTCCCCACATTACCCAGAGGGCTGCATTTTTCCAACCTTTCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54233016..54233087 26863196 MeRIP-seq:(Medium) rs1330261307 Functional Loss SNV dbSNP153 33..33 33 - - - 90770 RMVar_ID_90770 Human_SNP_ID_501819437 m1A Human chr12 + 54233646 54233646 54233646 GATTTATCAACACATACAGTAAAATGTTCACTAGGGGCCGGGTGCGGTGGCTTATGCTTGTAATC GATTTATCAACACATACAGTAAAATGTTCACTGGGGGCCGGGTGCGGTGGCTTATGCTTGTAATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54233600..54233718 26863196 MeRIP-seq:(Medium) rs1413728671 Functional Loss SNV dbSNP153 33..33 33 - - - 90771 RMVar_ID_90771 Human_SNP_ID_501820958 m1A Human chr12 - 54240499 54240499 54240499 TTCATGGCCAGGCACAGTGGCTACCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGAA TTCATGGCCAGGCACAGTGGCTACCGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCAGGAGAA T C CBX5 Ensembl:ENSG00000094916 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs929535674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228596,Human_RBP_ID_422919,Human_RBP_ID_753164,Human_RBP_ID_11980657,Human_RBP_ID_19828553,Human_RBP_ID_24468597,Human_RBP_ID_26908583 RMVar_hsa_circ_112121,RMVar_hsa_circ_114284,RMVar_hsa_circ_157011,RMVar_hsa_circ_157012 90772 RMVar_ID_90772 Human_SNP_ID_501822343 m1A Human chr12 + 54246202 54246202 54246202 CTGGTTCCAGTCCTCTCTCAAAGCCCCGAGCGATATCATTGCTCTGCTATAAATAGAAGATAAAG CTGGTTCCAGTCCTCTCTCAAAGCCCCGAGCGGTATCATTGCTCTGCTATAAATAGAAGATAAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:54246151..54252266;chr12:54246151..54252267;chr12:54246151..54246225 26863196 MeRIP-seq:(Medium) rs1175677300 Functional Loss SNV dbSNP153 33..33 33 - - - 90773 RMVar_ID_90773 Human_SNP_ID_501825281 m1A Human chr12 - 54257601 54257601 54257601 GCGGACAGCTGACAGTTCTTCTTCAGAGGATGAGGAGGAGTATGTTGTGGAGAAGGTGCTAGACA GCGGACAGCTGACAGTTCTTCTTCAGAGGATGCGGAGGAGTATGTTGTGGAGAAGGTGCTAGACA T G CBX5 Ensembl:ENSG00000094916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:54257501..54258129;chr12:54257551..54257777;chr12:54257551..54257759;chr12:54257501..54257729;chr12:54252515..54258129 26863196 MeRIP-seq:(Medium) rs1479140046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1797313,Human_RBP_ID_6198732,Human_RBP_ID_11980859,Human_RBP_ID_22493507,Human_RBP_ID_23565784,Human_RBP_ID_27630933 Human_Splice_Rec_1376982,Human_Splice_Rec_1376983,Human_Splice_Rec_1376990,Human_Splice_Rec_1376991,Human_Splice_Rec_1377002,Human_Splice_Rec_1377003,Human_Splice_Rec_1377010,Human_Splice_Rec_1377011 Human_miRNA_ID_738725,Human_miRNA_ID_742746,Human_miRNA_ID_746748,Human_miRNA_ID_1539295,Human_miRNA_ID_1593371 RMVar_hsa_circ_157018,RMVar_hsa_circ_378226,RMVar_hsa_circ_8662,RMVar_hsa_circ_110166,RMVar_hsa_circ_157020 90774 RMVar_ID_90774 Human_SNP_ID_501825307 m1A Human chr12 - 54257677 54257677 54257677 GTCCTTTGCCTTTGCAGGGACCTGGTGGCCTTAGTCTTTCAGGTGGAACGGTGTGCGACATGGGA GTCCTTTGCCTTTGCAGGGACCTGGTGGCCTTGGTCTTTCAGGTGGAACGGTGTGCGACATGGGA T C CBX5 Ensembl:ENSG00000094916 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54257626..54257725 32194978 MeRIP-seq:(Medium) rs372177224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229761,Human_RBP_ID_4246690,Human_RBP_ID_6198736 Human_Splice_Rec_1376982,Human_Splice_Rec_1376990,Human_Splice_Rec_1377002,Human_Splice_Rec_1377010 Human_miRNA_ID_2701161 RMVar_hsa_circ_157018,RMVar_hsa_circ_378226,RMVar_hsa_circ_8662,RMVar_hsa_circ_110166,RMVar_hsa_circ_157020 90775 RMVar_ID_90775 Human_SNP_ID_501825308 m1A Human chr12 - 54257677 54257677 54257677 GTCCTTTGCCTTTGCAGGGACCTGGTGGCCTTAGTCTTTCAGGTGGAACGGTGTGCGACATGGGA GTCCTTTGCCTTTGCAGGGACCTGGTGGCCTTCGTCTTTCAGGTGGAACGGTGTGCGACATGGGA T G CBX5 Ensembl:ENSG00000094916 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54257626..54257725 32194978 MeRIP-seq:(Medium) rs372177224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229761,Human_RBP_ID_4246690,Human_RBP_ID_6198736 Human_Splice_Rec_1376982,Human_Splice_Rec_1376990,Human_Splice_Rec_1377002,Human_Splice_Rec_1377010 Human_miRNA_ID_2701161 RMVar_hsa_circ_157018,RMVar_hsa_circ_378226,RMVar_hsa_circ_8662,RMVar_hsa_circ_110166,RMVar_hsa_circ_157020 90776 RMVar_ID_90776 Human_SNP_ID_501830961 m1A Human chr12 + 54280078 54280078 54280078 TGTTCCTGTATGGTGAGGCCGCACCACAAGCCACCACCGCCGCCGCCTTCTGCGCAACGCCAACC TGTTCCTGTATGGTGAGGCCGCACCACAAGCCCCCACCGCCGCCGCCTTCTGCGCAACGCCAACC A C AC078778.1 Ensembl:ENSG00000258344 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:54279937..54280125 26863196 MeRIP-seq:(Medium) rs959502547 Functional Loss SNV dbSNP153 33..33 33 - - - 90777 RMVar_ID_90777 Human_SNP_ID_501832118 m1A Human chr12 - 54282664 54282662 54282665 TCAGAACTACATGTAGATAAACCATACATACCACGACCACTGAAGTTTCCTCCACGACCGAAGTT TCAGAACTACATGTAGATAAACCATACATAC___GACCACTGAAGTTTCCTCCACGACCGAAGTT CGTG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:54282477..54282933 26863196 MeRIP-seq:(Medium) rs750308539 Functional Loss DEL dbSNP153 32..34 33 - - - 90778 RMVar_ID_90778 Human_SNP_ID_501832209 m1A Human chr12 - 54282873 54282873 54282873 ATTTTTCTCTACTTATTCCTAAAAAACTTACCATCATTACCAAATCCATTATAGCCATCCCCACT ATTTTTCTCTACTTATTCCTAAAAAACTTACCGTCATTACCAAATCCATTATAGCCATCCCCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:54282826..54282900;chr12:54282810..54283753 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 90779 RMVar_ID_90779 Human_SNP_ID_501832268 m1A Human chr12 + 54283040 54283040 54283040 AGCCGTTACACTTGCACAAGTTTTCATTGTCAAATACTTTTGTCTTATTGAGAAGAATTGTATTC AGCCGTTACACTTGCACAAGTTTTCATTGTCAGATACTTTTGTCTTATTGAGAAGAATTGTATTC A G HNRNPA1,AC078778.1 Ensembl:ENSG00000135486,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54283037..54283301 26863196 MeRIP-seq:(Medium) rs750295573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1797349,Human_RBP_ID_2344515,Human_RBP_ID_11981345,Human_RBP_ID_22794571,Human_RBP_ID_24466945,Human_RBP_ID_24981870 RMVar_hsa_circ_112580,RMVar_hsa_circ_108254,RMVar_hsa_circ_117737,RMVar_hsa_circ_123666,RMVar_hsa_circ_157021,RMVar_hsa_circ_157026,RMVar_hsa_circ_157027,RMVar_hsa_circ_85995,RMVar_hsa_circ_123946,RMVar_hsa_circ_157029,RMVar_hsa_circ_157032,RMVar_hsa_circ_121684,RMVar_hsa_circ_122196,RMVar_hsa_circ_157035,RMVar_hsa_circ_157036,RMVar_hsa_circ_110463,RMVar_hsa_circ_157037,RMVar_hsa_circ_157040,RMVar_hsa_circ_116283,RMVar_hsa_circ_91661,RMVar_hsa_circ_157041,RMVar_hsa_circ_157039 90780 RMVar_ID_90780 Human_SNP_ID_501832292 m1A Human chr12 + 54283085 54283085 54283085 TATTGAGAAGAATTGTATTCTTGTAGGTGGTTATGGAGGAGGCGGCCCTGGTTACTCTGGAGGAA TATTGAGAAGAATTGTATTCTTGTAGGTGGTTTTGGAGGAGGCGGCCCTGGTTACTCTGGAGGAA A T HNRNPA1,AC078778.1 Ensembl:ENSG00000135486,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:54283076..54283250 26863196 MeRIP-seq:(Medium) rs368695365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2344516,Human_RBP_ID_4230474,Human_RBP_ID_5087445,Human_RBP_ID_5094404,Human_RBP_ID_5555473,Human_RBP_ID_6198830,Human_RBP_ID_9018498,Human_RBP_ID_9352756,Human_RBP_ID_9714488,Human_RBP_ID_11981346,Human_RBP_ID_17669048,Human_RBP_ID_17822463,Human_RBP_ID_22905723,Human_RBP_ID_23125680,Human_RBP_ID_23565826,Human_RBP_ID_24981871,Human_RBP_ID_27836755 Human_Splice_Rec_1377048 Human_miRNA_ID_2573764 RMVar_hsa_circ_2323,RMVar_hsa_circ_112580,RMVar_hsa_circ_108254,RMVar_hsa_circ_117737,RMVar_hsa_circ_123666,RMVar_hsa_circ_157021,RMVar_hsa_circ_157026,RMVar_hsa_circ_157027,RMVar_hsa_circ_85995,RMVar_hsa_circ_123946,RMVar_hsa_circ_157029,RMVar_hsa_circ_157032,RMVar_hsa_circ_121684,RMVar_hsa_circ_122196,RMVar_hsa_circ_157035,RMVar_hsa_circ_157036,RMVar_hsa_circ_110463,RMVar_hsa_circ_157037,RMVar_hsa_circ_157040,RMVar_hsa_circ_116283,RMVar_hsa_circ_91661,RMVar_hsa_circ_157041,RMVar_hsa_circ_157039,RMVar_hsa_circ_111547,RMVar_hsa_circ_157042 90781 RMVar_ID_90781 Human_SNP_ID_501832586 m1A Human chr12 - 54283849 54283849 54283849 CCAAAATTTGAAGACTGATTGTTGTAATTCCCAAAATCATTGTAGCTTCCACCACCTCCAAAATT CCAAAATTTGAAGACTGATTGTTGTAATTCCCCAAATCATTGTAGCTTCCACCACCTCCAAAATT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54282810..54283925 26863196 MeRIP-seq:(Medium) rs554269174 Functional Loss SNV dbSNP153 33..33 33 - - - 90782 RMVar_ID_90782 Human_SNP_ID_501832590 m1A Human chr12 + 54283853 54283853 54283853 TTGGAGGTGGTGGAAGCTACAATGATTTTGGGAATTACAACAATCAGTCTTCAAATTTTGGACCC TTGGAGGTGGTGGAAGCTACAATGATTTTGGGGATTACAACAATCAGTCTTCAAATTTTGGACCC A G HNRNPA1,AC078778.1 Ensembl:ENSG00000135486,Ensembl:ENSG00000258344 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54283801..54283900 26863196 MeRIP-seq:(Medium) rs483353023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32774,Human_RBP_ID_422992,Human_RBP_ID_752548,Human_RBP_ID_809860,Human_RBP_ID_875899,Human_RBP_ID_993279,Human_RBP_ID_1127927,Human_RBP_ID_1167471,Human_RBP_ID_1269789,Human_RBP_ID_1473977,Human_RBP_ID_1797353,Human_RBP_ID_2368414,Human_RBP_ID_3408891,Human_RBP_ID_4248548,Human_RBP_ID_5087448,Human_RBP_ID_5094406,Human_RBP_ID_5173715,Human_RBP_ID_5558130,Human_RBP_ID_5640970,Human_RBP_ID_5645375,Human_RBP_ID_6198850,Human_RBP_ID_8179978,Human_RBP_ID_8379400,Human_RBP_ID_8783256,Human_RBP_ID_9018499,Human_RBP_ID_11981384,Human_RBP_ID_17355150,Human_RBP_ID_17472333,Human_RBP_ID_17650688,Human_RBP_ID_17685759,Human_RBP_ID_17822465,Human_RBP_ID_18261884,Human_RBP_ID_18629201,Human_RBP_ID_19785354,Human_RBP_ID_22175416,Human_RBP_ID_22493512,Human_RBP_ID_22794572,Human_RBP_ID_22905743,Human_RBP_ID_23207653,Human_RBP_ID_23565833,Human_RBP_ID_26423786,Human_RBP_ID_26908645,Human_RBP_ID_27216053,Human_RBP_ID_27630941 Human_Splice_Rec_1377030,Human_Splice_Rec_1377050,Human_Splice_Rec_1377064,Human_Splice_Rec_1377078,Human_Splice_Rec_1377110,Human_Splice_Rec_1377126,Human_Splice_Rec_1377154 Human_miRNA_ID_1037867 Clinvar_Rec_512 RMVar_hsa_circ_112580,RMVar_hsa_circ_108254,RMVar_hsa_circ_117737,RMVar_hsa_circ_123666,RMVar_hsa_circ_157021,RMVar_hsa_circ_157026,RMVar_hsa_circ_157027,RMVar_hsa_circ_85995,RMVar_hsa_circ_123946,RMVar_hsa_circ_157029,RMVar_hsa_circ_157032,RMVar_hsa_circ_121684,RMVar_hsa_circ_122196,RMVar_hsa_circ_157035,RMVar_hsa_circ_157036,RMVar_hsa_circ_110463,RMVar_hsa_circ_157037,RMVar_hsa_circ_157040,RMVar_hsa_circ_91661,RMVar_hsa_circ_157041,RMVar_hsa_circ_111547,RMVar_hsa_circ_127464,RMVar_hsa_circ_157042,RMVar_hsa_circ_157043 90783 RMVar_ID_90783 Human_SNP_ID_501832592 m1A Human chr12 + 54283860 54283860 54283860 TGGTGGAAGCTACAATGATTTTGGGAATTACAACAATCAGTCTTCAAATTTTGGACCCATGAAGG TGGTGGAAGCTACAATGATTTTGGGAATTACAGCAATCAGTCTTCAAATTTTGGACCCATGAAGG A G HNRNPA1,AC078778.1 Ensembl:ENSG00000135486,Ensembl:ENSG00000258344 Protein coding,lincRNA CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:54283801..54283900 26863196 MeRIP-seq:(Medium) rs397518454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_422992,Human_RBP_ID_752548,Human_RBP_ID_809860,Human_RBP_ID_875899,Human_RBP_ID_993279,Human_RBP_ID_1127927,Human_RBP_ID_1167472,Human_RBP_ID_1269789,Human_RBP_ID_1473977,Human_RBP_ID_1797354,Human_RBP_ID_2368415,Human_RBP_ID_3408891,Human_RBP_ID_4248548,Human_RBP_ID_5087448,Human_RBP_ID_5094406,Human_RBP_ID_5173715,Human_RBP_ID_5558130,Human_RBP_ID_5640970,Human_RBP_ID_5645375,Human_RBP_ID_6198850,Human_RBP_ID_8179978,Human_RBP_ID_8379402,Human_RBP_ID_11981386,Human_RBP_ID_17355150,Human_RBP_ID_17472333,Human_RBP_ID_17650688,Human_RBP_ID_17822465,Human_RBP_ID_18261884,Human_RBP_ID_18629202,Human_RBP_ID_22001423,Human_RBP_ID_22493512,Human_RBP_ID_23207653,Human_RBP_ID_23565834,Human_RBP_ID_27630942 Human_Splice_Rec_1377030,Human_Splice_Rec_1377050,Human_Splice_Rec_1377064,Human_Splice_Rec_1377078,Human_Splice_Rec_1377110,Human_Splice_Rec_1377126,Human_Splice_Rec_1377154 Human_miRNA_ID_1037867 Clinvar_Rec_513 GWAS_ID_11689 RMVar_hsa_circ_112580,RMVar_hsa_circ_108254,RMVar_hsa_circ_117737,RMVar_hsa_circ_123666,RMVar_hsa_circ_157021,RMVar_hsa_circ_157026,RMVar_hsa_circ_157027,RMVar_hsa_circ_85995,RMVar_hsa_circ_123946,RMVar_hsa_circ_157029,RMVar_hsa_circ_157032,RMVar_hsa_circ_121684,RMVar_hsa_circ_122196,RMVar_hsa_circ_157035,RMVar_hsa_circ_157036,RMVar_hsa_circ_110463,RMVar_hsa_circ_157037,RMVar_hsa_circ_157040,RMVar_hsa_circ_91661,RMVar_hsa_circ_157041,RMVar_hsa_circ_111547,RMVar_hsa_circ_127464,RMVar_hsa_circ_157042,RMVar_hsa_circ_157043 90784 RMVar_ID_90784 Human_SNP_ID_501833201 m1A Human chr12 - 54285978 54285978 54285978 AGGCATTGTCACGAATCCTGAGGTATCTGCAAACTCCCTCAATAGTTAGGGTTCCACCTGCTATT AGGCATTGTCACGAATCCTGAGGTATCTGCAATCTCCCTCAATAGTTAGGGTTCCACCTGCTATT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54285935..54286023 26863196 MeRIP-seq:(Medium) rs528483188 Functional Loss SNV dbSNP153 33..33 33 - - - 90785 RMVar_ID_90785 Human_SNP_ID_501843287 m1A Human chr12 + 54325202 54325202 54325202 GCGCTGATTTTGGTAGGAGCTGGAGGGGCAGCAGAGATGCTGTGGTGTCCACAGGGGCCGGGAGT GCGCTGATTTTGGTAGGAGCTGGAGGGGCAGCGGAGATGCTGTGGTGTCCACAGGGGCCGGGAGT A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54325200..54325300 32194978 MeRIP-seq:(Medium) rs754600737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5349625,Human_RBP_ID_5560830,Human_RBP_ID_19056285 Human_Splice_Rec_1377373 RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 90786 RMVar_ID_90786 Human_SNP_ID_501847226 m1A Human chr12 - 54340533 54340533 54340533 CAGTATACAGGGAAGGTTCCTGAAGAGATACGAACATACCTTCAGTCCTGAAGCCTCCCATCACC CAGTATACAGGGAAGGTTCCTGAAGAGATACGGACATACCTTCAGTCCTGAAGCCTCCCATCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54340526..54340625 26863196 MeRIP-seq:(Medium) rs1483675362 Functional Loss SNV dbSNP153 33..33 33 - - - 90787 RMVar_ID_90787 Human_SNP_ID_501847931 m1A Human chr12 + 54343243 54343243 54343243 TTTTCCCCCACCAGGTGAAATTGCCCTCTTGGAAGGCCTGACAGTGGTATACAAAAGCAGTATAG TTTTCCCCCACCAGGTGAAATTGCCCTCTTGGGAGGCCTGACAGTGGTATACAAAAGCAGTATAG A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA CDS,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1351519009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32770,Human_RBP_ID_423050,Human_RBP_ID_993299,Human_RBP_ID_1127783,Human_RBP_ID_1474052,Human_RBP_ID_4248555,Human_RBP_ID_5347389,Human_RBP_ID_17357116,Human_RBP_ID_18434413,Human_RBP_ID_18975703,Human_RBP_ID_22437755,Human_RBP_ID_22644891,Human_RBP_ID_23565916,Human_RBP_ID_27154898,Human_RBP_ID_27630973 Human_Splice_Rec_1377192,Human_Splice_Rec_1377193,Human_Splice_Rec_1377200,Human_Splice_Rec_1377210,Human_Splice_Rec_1377211,Human_Splice_Rec_1377226,Human_Splice_Rec_1377227,Human_Splice_Rec_1377240,Human_Splice_Rec_1377241,Human_Splice_Rec_1377258,Human_Splice_Rec_1377259,Human_Splice_Rec_1377274,Human_Splice_Rec_1377275,Human_Splice_Rec_1377284,Human_Splice_Rec_1377285,Human_Splice_Rec_1377294,Human_Splice_Rec_1377295,Human_Splice_Rec_1377310,Human_Splice_Rec_1377311,Human_Splice_Rec_1377322,Human_Splice_Rec_1377323,Human_Splice_Rec_1377364,Human_Splice_Rec_1377365,Human_Splice_Rec_1377392,Human_Splice_Rec_1377393,Human_Splice_Rec_1377406,Human_Splice_Rec_1377407 Human_miRNA_ID_1966129,Human_miRNA_ID_2361587 RMVar_hsa_circ_19095,RMVar_hsa_circ_98206,RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_317884,RMVar_hsa_circ_342190,RMVar_hsa_circ_157049,RMVar_hsa_circ_271710,RMVar_hsa_circ_157052,RMVar_hsa_circ_43942,RMVar_hsa_circ_347432,RMVar_hsa_circ_157051,RMVar_hsa_circ_376493,RMVar_hsa_circ_325564,RMVar_hsa_circ_157056,RMVar_hsa_circ_300940,RMVar_hsa_circ_157054,RMVar_hsa_circ_340142,RMVar_hsa_circ_268885,RMVar_hsa_circ_157055 90788 RMVar_ID_90788 Human_SNP_ID_501849004 m1A Human chr12 + 54347842 54347842 54347842 CTGTTCTTGGCTGTGGATGAAATTGTAGATGGAGGGTAAGTTCTCTGACCTGCCTTGATCTTGGG CTGTTCTTGGCTGTGGATGAAATTGTAGATGGGGGGTAAGTTCTCTGACCTGCCTTGATCTTGGG A G COPZ1 Ensembl:ENSG00000111481 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54346626..54347867 32194978 MeRIP-seq:(Medium) rs1356669231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5347390,Human_RBP_ID_17357117,Human_RBP_ID_17650689,Human_RBP_ID_17830879,Human_RBP_ID_21885224,Human_RBP_ID_22437103,Human_RBP_ID_26421293 Human_Splice_Rec_1377214,Human_Splice_Rec_1377215,Human_Splice_Rec_1377228,Human_Splice_Rec_1377229,Human_Splice_Rec_1377246,Human_Splice_Rec_1377247,Human_Splice_Rec_1377262,Human_Splice_Rec_1377263,Human_Splice_Rec_1377278,Human_Splice_Rec_1377288,Human_Splice_Rec_1377289,Human_Splice_Rec_1377298,Human_Splice_Rec_1377299,Human_Splice_Rec_1377314,Human_Splice_Rec_1377315,Human_Splice_Rec_1377326,Human_Splice_Rec_1377327,Human_Splice_Rec_1377340,Human_Splice_Rec_1377341,Human_Splice_Rec_1377352,Human_Splice_Rec_1377353,Human_Splice_Rec_1377368,Human_Splice_Rec_1377369,Human_Splice_Rec_1377380,Human_Splice_Rec_1377381,Human_Splice_Rec_1377396,Human_Splice_Rec_1377397,Human_Splice_Rec_1377410 RMVar_hsa_circ_98206,RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_342190,RMVar_hsa_circ_157052,RMVar_hsa_circ_347432,RMVar_hsa_circ_157051,RMVar_hsa_circ_376493,RMVar_hsa_circ_157056,RMVar_hsa_circ_340142,RMVar_hsa_circ_268885,RMVar_hsa_circ_309803 90789 RMVar_ID_90789 Human_SNP_ID_501849648 m1A Human chr12 - 54350621 54350621 54350621 GAATGGAGATTTAAGGATCCCTGTGATCCCCGAGATGACCCTGAGAGCATCGATTGGGGAACTAG GAATGGAGATTTAAGGATCCCTGTGATCCCCGGGATGACCCTGAGAGCATCGATTGGGGAACTAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54350466..54350675 32194978 MeRIP-seq:(Medium) rs1432141547 Functional Loss SNV dbSNP153 33..33 33 - - - 90790 RMVar_ID_90790 Human_SNP_ID_501849686 m1A Human chr12 - 54350774 54350774 54350774 GGGAGCATGTGAGCATAATCCAGTCTAGAAAGAAAGAGGGTGCTTCCCCTGCCCTATTATCTAAA GGGAGCATGTGAGCATAATCCAGTCTAGAAAGTAAGAGGGTGCTTCCCCTGCCCTATTATCTAAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:54350751..54350775 26863196 MeRIP-seq:(Medium) rs1026635213 Functional Loss SNV dbSNP153 33..33 33 - - - 90791 RMVar_ID_90791 Human_SNP_ID_501851418 m1A Human chr12 + 54358573 54358573 54358573 CCTATTGCGCCTTTCTCTGTCTTTGCTTCTCTAATGCTTTTCCTTTTCAGAGCCATTGTGTGAAA CCTATTGCGCCTTTCTCTGTCTTTGCTTCTCTGATGCTTTTCCTTTTCAGAGCCATTGTGTGAAA A G AC079313.1,AC079313.2 Ensembl:ENSG00000258086,Ensembl:ENSG00000258137 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54358446..54358583 26863196 MeRIP-seq:(Medium) rs1313567995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19824099 90792 RMVar_ID_90792 Human_SNP_ID_501853986 m1A Human chr12 + 54369310 54369310 54369310 TCGGCGGCTGAAGGGTTGACGATACGGAAACCACGGAGTCGGGGGTGGGGGAGAGGTGTCACACC TCGGCGGCTGAAGGGTTGACGATACGGAAACCGCGGAGTCGGGGGTGGGGGAGAGGTGTCACACC A G AC079313.1,AC079313.2 Ensembl:ENSG00000258086,Ensembl:ENSG00000258137 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54369181..54369703 26863196 MeRIP-seq:(Medium) rs1379665040 Functional Loss SNV dbSNP153 33..33 33 - - - 90793 RMVar_ID_90793 Human_SNP_ID_501854061 m1A Human chr12 - 54369709 54369709 54369709 CGCCTGCAACCTCACTGTGCCCGCCCCGCACCATGCCCTAGCCCCAGGTCTAGCCGGGCCCATTG CGCCTGCAACCTCACTGTGCCCGCCCCGCACCTTGCCCTAGCCCCAGGTCTAGCCGGGCCCATTG T A ZNF385A Ensembl:ENSG00000161642 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:54369590..54369750 26863196 MeRIP-seq:(Medium) rs1440519192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5314576,Human_RBP_ID_8178005,Human_RBP_ID_26421319 90794 RMVar_ID_90794 Human_SNP_ID_501854161 m1A Human chr12 - 54370070 54370070 54370070 TAGCGGGGGAGGGGGGCTTCAGAAGGGGGGGAACACCCCAGATCTCAGGGAACCCCGCCCCCTGC TAGCGGGGGAGGGGGGCTTCAGAAGGGGGGGAGCACCCCAGATCTCAGGGAACCCCGCCCCCTGC T C ZNF385A Ensembl:ENSG00000161642 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:54370026..54370126 32194978 MeRIP-seq:(Medium) rs1293327004 Functional Loss SNV dbSNP153 33..33 33 - - - 90795 RMVar_ID_90795 Human_SNP_ID_501854272 m1A Human chr12 + 54370317 54370317 54370317 GCGCAGTTCGGATGGGTCCGGGGGCCGGGTGAAGCAGAGGGTGAGTGATCGGCGGTCCCTGGAGA GCGCAGTTCGGATGGGTCCGGGGGCCGGGTGAGGCAGAGGGTGAGTGATCGGCGGTCCCTGGAGA A G AC079313.1,AC079313.2 Ensembl:ENSG00000258086,Ensembl:ENSG00000258137 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54370270..54370366 26863196 MeRIP-seq:(Medium) rs1260052661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121617,RMVar_hsa_circ_157059 90796 RMVar_ID_90796 Human_SNP_ID_501854286 m1A Human chr12 - 54370361 54370361 54370361 GCAGGCTCGCCGCTGTCCCTGCGCCCGGCTCCAGCCGCACCTCTTCTCCAGGGACCGCCGATCAC GCAGGCTCGCCGCTGTCCCTGCGCCCGGCTCCGGCCGCACCTCTTCTCCAGGGACCGCCGATCAC T C ZNF385A Ensembl:ENSG00000161642 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:54370224..54370424 32194978 MeRIP-seq:(Medium) rs1382499007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8379491 90797 RMVar_ID_90797 Human_SNP_ID_501855293 m1A Human chr12 - 54374057 54374057 54374057 TCAAAGGCATTGAGGCTGCCAAGACCAGAGGCAGGGAGCCTGGCGTCCGAGAACCTGGAGACCCA TCAAAGGCATTGAGGCTGCCAAGACCAGAGGCTGGGAGCCTGGCGTCCGAGAACCTGGAGACCCA T A ZNF385A Ensembl:ENSG00000161642 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:54374007..54379125 32194978 MeRIP-seq:(Medium) rs1473164610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1377434,Human_Splice_Rec_1377435,Human_Splice_Rec_1377448,Human_Splice_Rec_1377449,Human_Splice_Rec_1377458,Human_Splice_Rec_1377459,Human_Splice_Rec_1377470,Human_Splice_Rec_1377471,Human_Splice_Rec_1377484,Human_Splice_Rec_1377485,Human_Splice_Rec_1377500,Human_Splice_Rec_1377501,Human_Splice_Rec_1377512,Human_Splice_Rec_1377513,Human_Splice_Rec_1377524,Human_Splice_Rec_1377525,Human_Splice_Rec_1377536,Human_Splice_Rec_1377537,Human_Splice_Rec_1377544,Human_Splice_Rec_1377545,Human_Splice_Rec_1377554,Human_Splice_Rec_1377555,Human_Splice_Rec_1377562,Human_Splice_Rec_1377563,Human_Splice_Rec_1377570,Human_Splice_Rec_1377571,Human_Splice_Rec_1377574,Human_Splice_Rec_1377575,Human_Splice_Rec_1377578,Human_Splice_Rec_1377579 RMVar_hsa_circ_37432 90798 RMVar_ID_90798 Human_SNP_ID_501861260 m1A Human chr12 - 54399949 54399949 54399949 AGATGGGAAAGGGGCCCAACACTTTCTTTTATAGTTGGATCCCGAGGGTTCCCTGCACCACCAGC AGATGGGAAAGGGGCCCAACACTTTCTTTTATTGTTGGATCCCGAGGGTTCCCTGCACCACCAGC T A ITGA5 Ensembl:ENSG00000161638 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54399901..54399950 32194978 MeRIP-seq:(Medium) rs150264488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_873665,Human_RBP_ID_3941707,Human_RBP_ID_5346632,Human_RBP_ID_19060242 Human_Splice_Rec_1377663,Human_Splice_Rec_1377671,Human_Splice_Rec_1377685 RMVar_hsa_circ_75942,RMVar_hsa_circ_120109,RMVar_hsa_circ_124881,RMVar_hsa_circ_106309,RMVar_hsa_circ_109909,RMVar_hsa_circ_106796,RMVar_hsa_circ_100190,RMVar_hsa_circ_101546,RMVar_hsa_circ_82395,RMVar_hsa_circ_100820,RMVar_hsa_circ_157062,RMVar_hsa_circ_157064,RMVar_hsa_circ_157066,RMVar_hsa_circ_157067,RMVar_hsa_circ_157065,RMVar_hsa_circ_157063,RMVar_hsa_circ_157060,RMVar_hsa_circ_157061,RMVar_hsa_circ_102686,RMVar_hsa_circ_91744,RMVar_hsa_circ_99314,RMVar_hsa_circ_83866,RMVar_hsa_circ_98254,RMVar_hsa_circ_157071,RMVar_hsa_circ_157073,RMVar_hsa_circ_157074,RMVar_hsa_circ_157075,RMVar_hsa_circ_157072,RMVar_hsa_circ_157070,RMVar_hsa_circ_99994,RMVar_hsa_circ_92691,RMVar_hsa_circ_97255,RMVar_hsa_circ_88670,RMVar_hsa_circ_157080,RMVar_hsa_circ_52900,RMVar_hsa_circ_75774,RMVar_hsa_circ_157082,RMVar_hsa_circ_157083,RMVar_hsa_circ_157081,RMVar_hsa_circ_157078,RMVar_hsa_circ_157079,RMVar_hsa_circ_81377,RMVar_hsa_circ_117184,RMVar_hsa_circ_345010,RMVar_hsa_circ_157084,RMVar_hsa_circ_157085,RMVar_hsa_circ_52541 90799 RMVar_ID_90799 Human_SNP_ID_501861261 m1A Human chr12 - 54399949 54399949 54399949 AGATGGGAAAGGGGCCCAACACTTTCTTTTATAGTTGGATCCCGAGGGTTCCCTGCACCACCAGC AGATGGGAAAGGGGCCCAACACTTTCTTTTATGGTTGGATCCCGAGGGTTCCCTGCACCACCAGC T C ITGA5 Ensembl:ENSG00000161638 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:54399901..54399950 32194978 MeRIP-seq:(Medium) rs150264488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_873665,Human_RBP_ID_3941707,Human_RBP_ID_5346632,Human_RBP_ID_19060242 Human_Splice_Rec_1377663,Human_Splice_Rec_1377671,Human_Splice_Rec_1377685 RMVar_hsa_circ_75942,RMVar_hsa_circ_120109,RMVar_hsa_circ_124881,RMVar_hsa_circ_106309,RMVar_hsa_circ_109909,RMVar_hsa_circ_106796,RMVar_hsa_circ_100190,RMVar_hsa_circ_101546,RMVar_hsa_circ_82395,RMVar_hsa_circ_100820,RMVar_hsa_circ_157062,RMVar_hsa_circ_157064,RMVar_hsa_circ_157066,RMVar_hsa_circ_157067,RMVar_hsa_circ_157065,RMVar_hsa_circ_157063,RMVar_hsa_circ_157060,RMVar_hsa_circ_157061,RMVar_hsa_circ_102686,RMVar_hsa_circ_91744,RMVar_hsa_circ_99314,RMVar_hsa_circ_83866,RMVar_hsa_circ_98254,RMVar_hsa_circ_157071,RMVar_hsa_circ_157073,RMVar_hsa_circ_157074,RMVar_hsa_circ_157075,RMVar_hsa_circ_157072,RMVar_hsa_circ_157070,RMVar_hsa_circ_99994,RMVar_hsa_circ_92691,RMVar_hsa_circ_97255,RMVar_hsa_circ_88670,RMVar_hsa_circ_157080,RMVar_hsa_circ_52900,RMVar_hsa_circ_75774,RMVar_hsa_circ_157082,RMVar_hsa_circ_157083,RMVar_hsa_circ_157081,RMVar_hsa_circ_157078,RMVar_hsa_circ_157079,RMVar_hsa_circ_81377,RMVar_hsa_circ_117184,RMVar_hsa_circ_345010,RMVar_hsa_circ_157084,RMVar_hsa_circ_157085,RMVar_hsa_circ_52541 90800 RMVar_ID_90800 Human_SNP_ID_501862623 m1A Human chr12 + 54404802 54404802 54404802 GCTGGCTGCCCACAGGGGCTGCAGAACCTGGGAAGGCTTAGAGCCCAGCCCTCCTGGGCCCCCAG GCTGGCTGCCCACAGGGGCTGCAGAACCTGGGCAGGCTTAGAGCCCAGCCCTCCTGGGCCCCCAG A C AC079313.1,AC079313.2 Ensembl:ENSG00000258086,Ensembl:ENSG00000258137 lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:54404751..54404875 32194978 MeRIP-seq:(Medium) rs772093582 Functional Loss SNV dbSNP153 33..33 33 - - - 90801 RMVar_ID_90801 Human_SNP_ID_501865999 m1A Human chr12 - 54418670 54418670 54418670 GGGCCAAGGGAGAGGAGAGCGCGTGAATGGAGAGCTGAGGGTCTCTGGCTGAAGTCTGTGGGCTG GGGCCAAGGGAGAGGAGAGCGCGTGAATGGAGTGCTGAGGGTCTCTGGCTGAAGTCTGTGGGCTG T A ITGA5 Ensembl:ENSG00000161638 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54418663..54418780 26863196 MeRIP-seq:(Medium) rs537673212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418374,Human_RBP_ID_5314951,Human_RBP_ID_5347425,Human_RBP_ID_8070852,Human_RBP_ID_22471987 RMVar_hsa_circ_109035,RMVar_hsa_circ_157098,RMVar_hsa_circ_157101,RMVar_hsa_circ_90178 90802 RMVar_ID_90802 Human_SNP_ID_501866132 m1A Human chr12 - 54419087 54419087 54419087 CGCTGCTGTTGCTGCTGCTGCCGCCGCCACCCAGGGTCGGGGGCTTCAACTTAGACGCGGAGGCC CGCTGCTGTTGCTGCTGCTGCCGCCGCCACCCGGGGTCGGGGGCTTCAACTTAGACGCGGAGGCC T C ITGA5 Ensembl:ENSG00000161638 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:54419037..54419215;chr12:54419039..54419211 26863196 MeRIP-seq:(Medium) rs1414979719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322540,Human_RBP_ID_22435922 RMVar_hsa_circ_109035,RMVar_hsa_circ_157098,RMVar_hsa_circ_157101,RMVar_hsa_circ_90178 90803 RMVar_ID_90803 Human_SNP_ID_502209490 m1A Human chr12 + 55684718 55684718 55684718 ACAACCTCCTCCCCGACCCTCTAGGTTAAGGCACTTCCGGGGAGGCAGGTCCTTGGGGTCCTGTT ACAACCTCCTCCCCGACCCTCTAGGTTAAGGCGCTTCCGGGGAGGCAGGTCCTTGGGGTCCTGTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55684667..55684817 32194978 MeRIP-seq:(Medium) rs991368794 Functional Loss SNV dbSNP153 33..33 33 - - - 90804 RMVar_ID_90804 Human_SNP_ID_502214235 m1A Human chr12 - 55701011 55701011 55701011 TTGGATGGTGGGGAATGGAAGTTCTGTGAGGGACGCCCCCAAGGCCATGAACAATTTGGGTTCTG TTGGATGGTGGGGAATGGAAGTTCTGTGAGGGGCGCCCCCAAGGCCATGAACAATTTGGGTTCTG T C ITGA7 Ensembl:ENSG00000135424 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55700845..55702979 32194978 MeRIP-seq:(Medium) rs552091036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157111,RMVar_hsa_circ_277038 90805 RMVar_ID_90805 Human_SNP_ID_502215871 m1A Human chr12 - 55707553 55707553 55707553 CCTTCAATCTGGACGTGATGGGTGCCTTGCGCAAGGAGGGCGAGCCAGGCAGCCTCTTCGGCTTC CCTTCAATCTGGACGTGATGGGTGCCTTGCGCTAGGAGGGCGAGCCAGGCAGCCTCTTCGGCTTC T A ITGA7 Ensembl:ENSG00000135424 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55703077..55707725 32194978 MeRIP-seq:(Medium) rs112775765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1378637,Human_Splice_Rec_1378685,Human_Splice_Rec_1378755,Human_Splice_Rec_1378851,Human_Splice_Rec_1378979 90806 RMVar_ID_90806 Human_SNP_ID_502218775 m1A Human chr12 + 55719171 55719171 55719171 GACCCTACAGGTCCAGGCTGCCCAATTTGCCAAGCAGACAGGCCAGTGGATCGGAATGGTGGAGA GACCCTACAGGTCCAGGCTGCCCAATTTGCCACGCAGACAGGCCAGTGGATCGGAATGGTGGAGA A C BLOC1S1,AC009779.4 Ensembl:ENSG00000135441,Ensembl:ENSG00000258311 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55719051..55719200 26863196 MeRIP-seq:(Medium) rs756388521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34770,Human_RBP_ID_423173,Human_RBP_ID_5112128,Human_RBP_ID_9018572,Human_RBP_ID_23566055 Human_Splice_Rec_1378982,Human_Splice_Rec_1378983,Human_Splice_Rec_1378988,Human_Splice_Rec_1378989,Human_Splice_Rec_1378994,Human_Splice_Rec_1378995,Human_Splice_Rec_1379000,Human_Splice_Rec_1379001,Human_Splice_Rec_1379006,Human_Splice_Rec_1379007,Human_Splice_Rec_1379012,Human_Splice_Rec_1379014,Human_Splice_Rec_1379015,Human_Splice_Rec_1379020,Human_Splice_Rec_1379021,Human_Splice_Rec_1379026,Human_Splice_Rec_1379028,Human_Splice_Rec_1379029 Human_miRNA_ID_604471,Human_miRNA_ID_604472,Human_miRNA_ID_2132439,Human_miRNA_ID_2155916,Human_miRNA_ID_2159477,Human_miRNA_ID_2225408,Human_miRNA_ID_2968928 RMVar_hsa_circ_10112,RMVar_hsa_circ_77226,RMVar_hsa_circ_157112 90807 RMVar_ID_90807 Human_SNP_ID_502218776 m1A Human chr12 + 55719171 55719171 55719171 GACCCTACAGGTCCAGGCTGCCCAATTTGCCAAGCAGACAGGCCAGTGGATCGGAATGGTGGAGA GACCCTACAGGTCCAGGCTGCCCAATTTGCCAGGCAGACAGGCCAGTGGATCGGAATGGTGGAGA A G BLOC1S1,AC009779.4 Ensembl:ENSG00000135441,Ensembl:ENSG00000258311 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55719051..55719200 26863196 MeRIP-seq:(Medium) rs756388521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34770,Human_RBP_ID_423173,Human_RBP_ID_5112128,Human_RBP_ID_9018572,Human_RBP_ID_23566055 Human_Splice_Rec_1378982,Human_Splice_Rec_1378983,Human_Splice_Rec_1378988,Human_Splice_Rec_1378989,Human_Splice_Rec_1378994,Human_Splice_Rec_1378995,Human_Splice_Rec_1379000,Human_Splice_Rec_1379001,Human_Splice_Rec_1379006,Human_Splice_Rec_1379007,Human_Splice_Rec_1379012,Human_Splice_Rec_1379014,Human_Splice_Rec_1379015,Human_Splice_Rec_1379020,Human_Splice_Rec_1379021,Human_Splice_Rec_1379026,Human_Splice_Rec_1379028,Human_Splice_Rec_1379029 Human_miRNA_ID_604471,Human_miRNA_ID_604472,Human_miRNA_ID_2132439,Human_miRNA_ID_2155916,Human_miRNA_ID_2159477,Human_miRNA_ID_2225408,Human_miRNA_ID_2968928 RMVar_hsa_circ_10112,RMVar_hsa_circ_77226,RMVar_hsa_circ_157112 90808 RMVar_ID_90808 Human_SNP_ID_502220852 m1A Human chr12 + 55726172 55726171 55726173 TCGTTGAAATTAATCCCACAGCCCACAGTAACATTAATGCAGCAGGAGTCGGGGACTCGGTTCTT TCGTTGAAATTAATCCCACAGCCCACAGTAAC__TAATGCAGCAGGAGTCGGGGACTCGGTTCTT CAT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55726101..55726275 32194978 MeRIP-seq:(Medium) rs774802256 Functional Loss DEL dbSNP153 33..34 33 - - - 90809 RMVar_ID_90809 Human_SNP_ID_502220862 m1A Human chr12 - 55726203 55726203 55726203 CACAGATTGGGAGAAAATCCCTTCCATGTCGAAGAACCGAGTCCCCGACTCCTGCTGCATTAATG CACAGATTGGGAGAAAATCCCTTCCATGTCGAGGAACCGAGTCCCCGACTCCTGCTGCATTAATG T C CD63 Ensembl:ENSG00000135404 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55726081..55726202 26863196 MeRIP-seq:(Medium) rs1192640637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1474094,Human_RBP_ID_5111473,Human_RBP_ID_18977256,Human_RBP_ID_22437114,Human_RBP_ID_22755964 Human_Splice_Rec_1379086,Human_Splice_Rec_1379087,Human_Splice_Rec_1379100,Human_Splice_Rec_1379101,Human_Splice_Rec_1379105,Human_Splice_Rec_1379112,Human_Splice_Rec_1379113,Human_Splice_Rec_1379120,Human_Splice_Rec_1379121,Human_Splice_Rec_1379132,Human_Splice_Rec_1379133,Human_Splice_Rec_1379144,Human_Splice_Rec_1379145,Human_Splice_Rec_1379158,Human_Splice_Rec_1379159,Human_Splice_Rec_1379172,Human_Splice_Rec_1379173,Human_Splice_Rec_1379184,Human_Splice_Rec_1379185,Human_Splice_Rec_1379196,Human_Splice_Rec_1379197,Human_Splice_Rec_1379208,Human_Splice_Rec_1379209,Human_Splice_Rec_1379224,Human_Splice_Rec_1379225,Human_Splice_Rec_1379236,Human_Splice_Rec_1379237 RMVar_hsa_circ_90672,RMVar_hsa_circ_100926,RMVar_hsa_circ_157113,RMVar_hsa_circ_55281,RMVar_hsa_circ_265808,RMVar_hsa_circ_157115 90810 RMVar_ID_90810 Human_SNP_ID_502221307 m1A Human chr12 + 55727319 55727319 55727319 CTCAGGACAAGCTGTGCCCCGACACCCACGGCAATCAGTCCCACTGCACAGGCCTAAGAGAAAAT CTCAGGACAAGCTGTGCCCCGACACCCACGGCGATCAGTCCCACTGCACAGGCCTAAGAGAAAAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55727113..55727655 26863196 MeRIP-seq:(Medium) rs772847145 Functional Loss SNV dbSNP153 33..33 33 - - - 90811 RMVar_ID_90811 Human_SNP_ID_502221586 m1A Human chr12 + 55728340 55728340 55728340 ACTTCACACATTTCATTCCTCCTTCCACCGCCATGGCTGCCGGGCCTGGGGCAGAGGGGAGGGCG ACTTCACACATTTCATTCCTCCTTCCACCGCCGTGGCTGCCGGGCCTGGGGCAGAGGGGAGGGCG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:55728276..55728375 26863410 MeRIP-seq:(Medium) rs1388589252 Functional Loss SNV dbSNP153 33..33 33 - - - 90812 RMVar_ID_90812 Human_SNP_ID_502224957 m1A Human chr12 - 55742334 55742332 55742335 GGGAGCACAGAGAGCCCAGGGGACAGAGGTGGAGAACTTGAGACCAGAGGAGCTCTAGCCACCAG GGGAGCACAGAGAGCCCAGGGGACAGAGGTG___AACTTGAGACCAGAGGAGCTCTAGCCACCAG TCTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55742307..55742405 26863196 MeRIP-seq:(Medium) rs1023905778 Functional Loss DEL dbSNP153 32..34 33 - - - 90813 RMVar_ID_90813 Human_SNP_ID_502225310 m1A Human chr12 + 55743433 55743409 55743433 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GCGGCGGCG________________________GCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GGCGGCGGCGGCGGCGGCGGCGGCA G GDF11 Ensembl:ENSG00000135414 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55743311..55743582;chr12:55743297..55743578;chr12:55743322..55743545 26863196 MeRIP-seq:(Medium) rs1317185115 Functional Loss DEL dbSNP153 10..33 33 - - - 90814 RMVar_ID_90814 Human_SNP_ID_502225313 m1A Human chr12 + 55743433 55743418 55743433 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GCGGCGGCGGCGGCGGCG_______________GCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GGCGGCGGCGGCGGCA G GDF11 Ensembl:ENSG00000135414 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55743311..55743582;chr12:55743297..55743578;chr12:55743322..55743545 26863196 MeRIP-seq:(Medium) rs901727853 Functional Loss DEL dbSNP153 19..33 33 - - - 90815 RMVar_ID_90815 Human_SNP_ID_502225317 m1A Human chr12 + 55743433 55743421 55743433 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GCGGCGGCGGCGGCGGCGGCG____________GCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GGCGGCGGCGGCA G GDF11 Ensembl:ENSG00000135414 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55743311..55743582;chr12:55743297..55743578;chr12:55743322..55743545 26863196 MeRIP-seq:(Medium) rs775952328 Functional Loss DEL dbSNP153,HGVD 22..33 33 - - - 90816 RMVar_ID_90816 Human_SNP_ID_502225321 m1A Human chr12 + 55743433 55743424 55743433 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GCGGCGGCGGCGGCGGCGGCGGCG_________GCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GGCGGCGGCA G GDF11 Ensembl:ENSG00000135414 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55743311..55743582;chr12:55743297..55743578;chr12:55743322..55743545 26863196 MeRIP-seq:(Medium) rs1328652957 Functional Loss DEL dbSNP153 25..33 33 - - - 90817 RMVar_ID_90817 Human_SNP_ID_502225327 m1A Human chr12 + 55743433 55743433 55743433 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGTCGGGGGGGAGCGCTCCAGCCG A G GDF11 Ensembl:ENSG00000135414 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55743311..55743582;chr12:55743297..55743578;chr12:55743322..55743545 26863196 MeRIP-seq:(Medium) rs1048961730 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 90818 RMVar_ID_90818 Human_SNP_ID_502226997 m1A Human chr12 + 55750136 55750133 55750137 GAAGTTTGCAGATGAGAAGGTTTGACAAAAAGACAGAGAGATGTAGAGACAGTGATAGAGACAGA GAAGTTTGCAGATGAGAAGGTTTGACAAAA____AGAGAGATGTAGAGACAGTGATAGAGACAGA AAGAC A GDF11 Ensembl:ENSG00000135414 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:55749992..55750272;chr12:55750035..55750249 26863196 MeRIP-seq:(Medium) rs983433287 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3408989,Human_RBP_ID_11982218,Human_RBP_ID_18261956,Human_RBP_ID_23566102 90819 RMVar_ID_90819 Human_SNP_ID_502227008 m1A Human chr12 + 55750180 55750180 55750180 AGAGACAGTGATAGAGACAGAGGAACAAAAAGAGCAGCAGTGAGAAGGCAAAGAGAGAGGCAGAA AGAGACAGTGATAGAGACAGAGGAACAAAAAGTGCAGCAGTGAGAAGGCAAAGAGAGAGGCAGAA A T GDF11 Ensembl:ENSG00000135414 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:55750064..55750363 26863196 MeRIP-seq:(Medium) rs538037846 Functional Loss SNV dbSNP153 33..33 33 - - - 90820 RMVar_ID_90820 Human_SNP_ID_502227286 m1A Human chr12 + 55751383 55751383 55751383 TTGCCATTTCAAGTCACTAGCTAGGCCCATTCATTCCTCCCACAACCCTGACCCATTCTCCTCTG TTGCCATTTCAAGTCACTAGCTAGGCCCATTCGTTCCTCCCACAACCCTGACCCATTCTCCTCTG A G GDF11 Ensembl:ENSG00000135414 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55751332..55751437 32194978 MeRIP-seq:(Medium) rs1252021235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17822614,Human_RBP_ID_27423325 90821 RMVar_ID_90821 Human_SNP_ID_502239520 m1A Human chr12 - 55800620 55800620 55800620 CACCTTGTTTCATTTGGTTTTAGGAAGAAGAAACAAAGCCCATTGAGCTCCCTGTCAAAGAGGAA CACCTTGTTTCATTTGGTTTTAGGAAGAAGAACCAAAGCCCATTGAGCTCCCTGTCAAAGAGGAA T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55800519..55817725 26863196 MeRIP-seq:(Medium) rs558277429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5347438,Human_RBP_ID_9364991,Human_RBP_ID_11983154,Human_RBP_ID_18977261,Human_RBP_ID_22646485,Human_RBP_ID_22910527,Human_RBP_ID_24543068,Human_RBP_ID_25015553,Human_RBP_ID_26321503 Human_Splice_Rec_1379266,Human_Splice_Rec_1379267,Human_Splice_Rec_1379286,Human_Splice_Rec_1379287,Human_Splice_Rec_1379308,Human_Splice_Rec_1379309,Human_Splice_Rec_1379330,Human_Splice_Rec_1379331,Human_Splice_Rec_1379348,Human_Splice_Rec_1379349,Human_Splice_Rec_1379370,Human_Splice_Rec_1379371 RMVar_hsa_circ_122717,RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_296409,RMVar_hsa_circ_343802,RMVar_hsa_circ_276457,RMVar_hsa_circ_157118,RMVar_hsa_circ_157119,RMVar_hsa_circ_310136,RMVar_hsa_circ_127815,RMVar_hsa_circ_157121,RMVar_hsa_circ_311987,RMVar_hsa_circ_275257,RMVar_hsa_circ_157122 90822 RMVar_ID_90822 Human_SNP_ID_502243959 m1A Human chr12 - 55817669 55817669 55817669 ATGGCGACCGAGACGGTGGAGCTCCATAAGCTAAAGGTACCGTGAATCGGGGAAGGGCTGAGTTG ATGGCGACCGAGACGGTGGAGCTCCATAAGCTTAAGGTACCGTGAATCGGGGAAGGGCTGAGTTG T A AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55796032..55817725 26863196 MeRIP-seq:(Medium) rs1322790719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555487,Human_RBP_ID_9364995,Human_RBP_ID_11983464,Human_RBP_ID_18417279,Human_RBP_ID_19056295,Human_RBP_ID_26321505,Human_RBP_ID_27805499 Human_Splice_Rec_1379261,Human_Splice_Rec_1379283,Human_Splice_Rec_1379303,Human_Splice_Rec_1379325,Human_Splice_Rec_1379343,Human_Splice_Rec_1379391,Human_Splice_Rec_1379409 RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 90823 RMVar_ID_90823 Human_SNP_ID_502243960 m1A Human chr12 - 55817669 55817669 55817669 ATGGCGACCGAGACGGTGGAGCTCCATAAGCTAAAGGTACCGTGAATCGGGGAAGGGCTGAGTTG ATGGCGACCGAGACGGTGGAGCTCCATAAGCTGAAGGTACCGTGAATCGGGGAAGGGCTGAGTTG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55796032..55817725 26863196 MeRIP-seq:(Medium) rs1322790719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555487,Human_RBP_ID_9364995,Human_RBP_ID_11983464,Human_RBP_ID_18417279,Human_RBP_ID_19056295,Human_RBP_ID_26321505,Human_RBP_ID_27805499 Human_Splice_Rec_1379261,Human_Splice_Rec_1379283,Human_Splice_Rec_1379303,Human_Splice_Rec_1379325,Human_Splice_Rec_1379343,Human_Splice_Rec_1379391,Human_Splice_Rec_1379409 RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 90824 RMVar_ID_90824 Human_SNP_ID_502244177 m1A Human chr12 - 55818102 55818102 55818102 TTACAGTCTTTGCAGCTCCTACCTGCCAGCTCAGATCCCCGTCCGGCTATGGGCGCGGCGCCGGC TTACAGTCTTTGCAGCTCCTACCTGCCAGCTCGGATCCCCGTCCGGCTATGGGCGCGGCGCCGGC T C AC023055.1 Ensembl:ENSG00000257390 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:55818051..55818165;chr12:55818051..55818256;chr12:55818051..55818186 26863196 MeRIP-seq:(Medium) rs1352050735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1379390,Human_Splice_Rec_1379408 90825 RMVar_ID_90825 Human_SNP_ID_502244181 m1A Human chr12 - 55818107 55818107 55818107 AACCCTTACAGTCTTTGCAGCTCCTACCTGCCAGCTCAGATCCCCGTCCGGCTATGGGCGCGGCG AACCCTTACAGTCTTTGCAGCTCCTACCTGCCCGCTCAGATCCCCGTCCGGCTATGGGCGCGGCG T G AC023055.1 Ensembl:ENSG00000257390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55818051..55818382 26863196 MeRIP-seq:(Medium) rs1373352591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19786462 Human_Splice_Rec_1379390,Human_Splice_Rec_1379408 90826 RMVar_ID_90826 Human_SNP_ID_502244183 m1A Human chr12 + 55818111 55818111 55818111 GCGCCCATAGCCGGACGGGGATCTGAGCTGGCAGGTAGGAGCTGCAAAGACTGTAAGGGTTGCTG GCGCCCATAGCCGGACGGGGATCTGAGCTGGCGGGTAGGAGCTGCAAAGACTGTAAGGGTTGCTG A G ORMDL2 Ensembl:ENSG00000123353 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:55818051..55818161 26863410 MeRIP-seq:(Medium) rs1325544682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229907,Human_RBP_ID_755265,Human_RBP_ID_4246719,Human_RBP_ID_18417280 Human_Splice_Rec_1379421,Human_Splice_Rec_1379427,Human_Splice_Rec_1379433 90827 RMVar_ID_90827 Human_SNP_ID_502244388 m1A Human chr12 - 55818979 55818979 55818979 CCCCACATTCATCCTAGCCGTAATGGGGGATCAGGCAGGAGTCCAGCTCAGTTTTTTCTCAACCC CCCCACATTCATCCTAGCCGTAATGGGGGATCTGGCAGGAGTCCAGCTCAGTTTTTTCTCAACCC T A AC023055.1 Ensembl:ENSG00000257390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:55818976..55819171;chr12:55818976..55819050 26863196 MeRIP-seq:(Medium) rs767985811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6199519,Human_RBP_ID_19786469 90828 RMVar_ID_90828 Human_SNP_ID_502244406 m1A Human chr12 - 55819013 55819013 55819013 CTCGGGTGTTGGGGTTTACTTCGCTGTGTGCCACCCCCACATTCATCCTAGCCGTAATGGGGGAT CTCGGGTGTTGGGGTTTACTTCGCTGTGTGCCCCCCCCACATTCATCCTAGCCGTAATGGGGGAT T G AC023055.1 Ensembl:ENSG00000257390 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:55818975..55819125 26863410 MeRIP-seq:(Medium) rs746878231 Functional Loss SNV dbSNP153 33..33 33 - - - 90829 RMVar_ID_90829 Human_SNP_ID_502246932 m1A Human chr12 + 55827855 55827855 55827855 AGTTGCCTGCAGGCATAGATGAGATGGCCACAAGTTTCTACGTACTCTCCCACCAATACCAGCAG AGTTGCCTGCAGGCATAGATGAGATGGCCACATGTTTCTACGTACTCTCCCACCAATACCAGCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:55827805..55828052;chr12:55827804..55827980 26863196 MeRIP-seq:(Medium) rs1271047520 Functional Loss SNV dbSNP153 33..33 33 - - - 90830 RMVar_ID_90830 Human_SNP_ID_502247171 m1A Human chr12 - 55828541 55828541 55828541 TGGACCCTGAAATACCTTCATTCTCAGGACTCAGGGACTCAGCAGGGACTGCTCCTAATGGTACC TGGACCCTGAAATACCTTCATTCTCAGGACTCCGGGACTCAGCAGGGACTGCTCCTAATGGTACC T G DNAJC14 Ensembl:ENSG00000135392 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55828424..55829151 32194978 MeRIP-seq:(Medium) rs747419407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36719,Human_RBP_ID_423335,Human_RBP_ID_1474139,Human_RBP_ID_1797469,Human_RBP_ID_4246722,Human_RBP_ID_6199596,Human_RBP_ID_8783336,Human_RBP_ID_9018608,Human_RBP_ID_11983635,Human_RBP_ID_17239526,Human_RBP_ID_17355203,Human_RBP_ID_17472394,Human_RBP_ID_18629375,Human_RBP_ID_27216220,Human_RBP_ID_27423367 90831 RMVar_ID_90831 Human_SNP_ID_502247423 m1A Human chr12 + 55829460 55829460 55829460 GAGCGAGACTCCATCTCAAAAAAACAAAAAAAAACGAAAAAAAAAAAAAAGACGGACGTACCGAA GAGCGAGACTCCATCTCAAAAAAACAAAAAAAGACGAAAAAAAAAAAAAAGACGGACGTACCGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:55829457..55829578 26863196 MeRIP-seq:(Medium) rs1317016282 Functional Loss SNV dbSNP153 33..33 33 - - - 90832 RMVar_ID_90832 Human_SNP_ID_502247436 m1A Human chr12 + 55829491 55829490 55829491 AAACGAAAAAAAAAAAAAAGACGGACGTACCGAAGAACGGCGGTAACTCCTCCCCCTCGAGCCGC AAACGAAAAAAAAAAAAAAGACGGACGTACCG_AGAACGGCGGTAACTCCTCCCCCTCGAGCCGC GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:55829479..55829581 26863196 MeRIP-seq:(Medium) rs1430698994 Functional Loss DEL dbSNP153 33..33 33 - - - 90833 RMVar_ID_90833 Human_SNP_ID_502247709 m1A Human chr12 - 55830399 55830399 55830399 GTATAAGGCTAGAGGCGTGTGCAGAGGAGGGGACCGACGGAACGGGGACCCAACTGGGTCTACGT GTATAAGGCTAGAGGCGTGTGCAGAGGAGGGGGCCGACGGAACGGGGACCCAACTGGGTCTACGT T C DNAJC14 Ensembl:ENSG00000135392 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:55830352..55830496 26863196 MeRIP-seq:(Medium) rs1391612485 Functional Loss SNV dbSNP153 33..33 33 - - - 90834 RMVar_ID_90834 Human_SNP_ID_502265515 m1A Human chr12 - 55901561 55901561 55901561 AAGAAAATCAGGTGGGTGGGAATCTCTTGGAGAACTGAGGCTGAGGGTAGAGGGAGTATGCCCAA AAGAAAATCAGGTGGGTGGGAATCTCTTGGAGGACTGAGGCTGAGGGTAGAGGGAGTATGCCCAA T C PYM1 Ensembl:ENSG00000170473 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55901511..55901611 32194978 MeRIP-seq:(Medium) rs1296960909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423362,Human_RBP_ID_2344859,Human_RBP_ID_5111960,Human_RBP_ID_6199628,Human_RBP_ID_26908860 Human_miRNA_ID_1539298,Human_miRNA_ID_2789589,Human_miRNA_ID_2789590,Human_miRNA_ID_2819200,Human_miRNA_ID_2819201 RMVar_hsa_circ_90586,RMVar_hsa_circ_127404,RMVar_hsa_circ_95992,RMVar_hsa_circ_157124,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 90835 RMVar_ID_90835 Human_SNP_ID_502265638 m1A Human chr12 - 55901908 55901908 55901908 CAGCTAGAAAAGCTAGCAAGGAGGAGGGCGCTAGAAGAGGAGTTAGAGGACTTGGAGTTAGGCCT CAGCTAGAAAAGCTAGCAAGGAGGAGGGCGCTGGAAGAGGAGTTAGAGGACTTGGAGTTAGGCCT T C PYM1 Ensembl:ENSG00000170473 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:55901857..55901981 26863196 MeRIP-seq:(Medium) rs775406472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6199639 RMVar_hsa_circ_90586,RMVar_hsa_circ_127404,RMVar_hsa_circ_95992,RMVar_hsa_circ_157124,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 90836 RMVar_ID_90836 Human_SNP_ID_502265758 m1A Human chr12 + 55902253 55902253 55902253 CGTTTGGCTGTCTTGGAGAGGCCTGGTTCACCACCTTCAGGCCTGGATGGGGTGACAGGAGCAGT CGTTTGGCTGTCTTGGAGAGGCCTGGTTCACCGCCTTCAGGCCTGGATGGGGTGACAGGAGCAGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55902204..55902353 32194978 MeRIP-seq:(Medium) rs1350177081 Functional Loss SNV dbSNP153 33..33 33 - - - 90837 RMVar_ID_90837 Human_SNP_ID_502272173 m1A Human chr12 + 55927024 55927024 55927024 TGGGCGGGGCACAGACCCCTTTCCAAGTCCGAACCCCTGCCCCGAGAGCCCGGAGAGAAGCGGCT TGGGCGGGGCACAGACCCCTTTCCAAGTCCGACCCCCTGCCCCGAGAGCCCGGAGAGAAGCGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55927019..55927102 26863196 MeRIP-seq:(Medium) rs915028054 Functional Loss SNV dbSNP153 33..33 33 - - - 90838 RMVar_ID_90838 Human_SNP_ID_502272431 m1A Human chr12 + 55927687 55927687 55927687 GCCAACCCACTCAACCACCAGAGACCCGCGGGAGGGGCGTGCAAGGCGGAGGGCGCCGCGGGTCG GCCAACCCACTCAACCACCAGAGACCCGCGGGTGGGGCGTGCAAGGCGGAGGGCGCCGCGGGTCG A T DGKA Ensembl:ENSG00000065357 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55927678..55927831 26863196 MeRIP-seq:(Medium) rs1449090598 Functional Loss SNV dbSNP153 33..33 33 - - - 90839 RMVar_ID_90839 Human_SNP_ID_502274619 m1A Human chr12 + 55936181 55936181 55936181 GATGAATCAAGATAGGTTGGGGGAGAGGGAGAAGGATCCAGAAATGGAGAGACAGAGATGAGTCA GATGAATCAAGATAGGTTGGGGGAGAGGGAGAGGGATCCAGAAATGGAGAGACAGAGATGAGTCA A G DGKA Ensembl:ENSG00000065357 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:55936131..55936238 26863196 MeRIP-seq:(Medium) rs1262409699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114667,RMVar_hsa_circ_157127 90840 RMVar_ID_90840 Human_SNP_ID_502282684 m1A Human chr12 - 55966952 55966952 55966952 CCGGCCCTGGAGCGGGGGCCTGGGAACCCTGCAGAAGGCGGACCCTGGCTCTCGGGGGCCGAGGA CCGGCCCTGGAGCGGGGGCCTGGGAACCCTGCCGAAGGCGGACCCTGGCTCTCGGGGGCCGAGGA T G PMEL,AC025162.1 Ensembl:ENSG00000185664,Ensembl:ENSG00000258554 Protein coding,lincRNA intron,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:55966851..55967050 26863410 MeRIP-seq:(Medium) rs1294359132 Functional Loss SNV dbSNP153 33..33 33 - - - 90841 RMVar_ID_90841 Human_SNP_ID_502282706 m1A Human chr12 - 55966996 55966996 55966996 ACCTTTTGGAAGTTCTCCATGAAGCGCCAGCGAGTCGGGTCAGCCCGGCCCTGGAGCGGGGGCCT ACCTTTTGGAAGTTCTCCATGAAGCGCCAGCGGGTCGGGTCAGCCCGGCCCTGGAGCGGGGGCCT T C PMEL,AC025162.1 Ensembl:ENSG00000185664,Ensembl:ENSG00000258554 Protein coding,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:55966826..55967050 26863196 MeRIP-seq:(Medium) rs1171451060 Functional Loss SNV dbSNP153 33..33 33 - - - 90842 RMVar_ID_90842 Human_SNP_ID_502282712 m1A Human chr12 - 55967000 55967000 55967000 TTCCACCTTTTGGAAGTTCTCCATGAAGCGCCAGCGAGTCGGGTCAGCCCGGCCCTGGAGCGGGG TTCCACCTTTTGGAAGTTCTCCATGAAGCGCCGGCGAGTCGGGTCAGCCCGGCCCTGGAGCGGGG T C PMEL,AC025162.1 Ensembl:ENSG00000185664,Ensembl:ENSG00000258554 Protein coding,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia chr12:55966826..55967050;chr12:55966897..55967050;chr12:55966951..55967239 26863196,32194978 MeRIP-seq:(Medium) rs917952705 Functional Loss SNV dbSNP153 33..33 33 - - - 90843 RMVar_ID_90843 Human_SNP_ID_502282713 m1A Human chr12 - 55967000 55967000 55967000 TTCCACCTTTTGGAAGTTCTCCATGAAGCGCCAGCGAGTCGGGTCAGCCCGGCCCTGGAGCGGGG TTCCACCTTTTGGAAGTTCTCCATGAAGCGCCCGCGAGTCGGGTCAGCCCGGCCCTGGAGCGGGG T G PMEL,AC025162.1 Ensembl:ENSG00000185664,Ensembl:ENSG00000258554 Protein coding,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia chr12:55966826..55967050;chr12:55966897..55967050;chr12:55966951..55967239 26863196,32194978 MeRIP-seq:(Medium) rs917952705 Functional Loss SNV dbSNP153 33..33 33 - - - 90844 RMVar_ID_90844 Human_SNP_ID_502283881 m1A Human chr12 + 55971651 55971651 55971651 ACTCTGATAGCCTTCTTGAAGCCCCCAGCCCTAATCTCACCCTCTCCTCCAGTGTGGGCTTGACC ACTCTGATAGCCTTCTTGAAGCCCCCAGCCCTGATCTCACCCTCTCCTCCAGTGTGGGCTTGACC A G CDK2 Ensembl:ENSG00000123374 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:55971601..55971675 26863196 MeRIP-seq:(Medium) rs1466798761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423396,Human_RBP_ID_5139630,Human_RBP_ID_5491758,Human_RBP_ID_17239535,Human_RBP_ID_17684864,Human_RBP_ID_17822748,Human_RBP_ID_24467009,Human_RBP_ID_27216255,Human_RBP_ID_27423416 Human_miRNA_ID_193532,Human_miRNA_ID_1261288,Human_miRNA_ID_1338945 90845 RMVar_ID_90845 Human_SNP_ID_502289067 m1A Human chr12 + 55992292 55992292 55992292 AAATAACCTCCATCCCTACCCCTCAGCACACAACCCCTACGGTAACAGCACACTGAGCCCTGGCT AAATAACCTCCATCCCTACCCCTCAGCACACAGCCCCTACGGTAACAGCACACTGAGCCCTGGCT A G RAB5B Ensembl:ENSG00000111540 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55992241..55992841 32194978 MeRIP-seq:(Medium) rs11550558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9255709,Human_RBP_ID_12084342,Human_RBP_ID_17475247,Human_RBP_ID_17667666,Human_RBP_ID_18527210,Human_RBP_ID_21968239 GWAS_ID_11690,GWAS_ID_11691,GWAS_ID_11692,GWAS_ID_11693,GWAS_ID_11694,GWAS_ID_11695,GWAS_ID_11696,GWAS_ID_11697,GWAS_ID_11698,GWAS_ID_11699 90846 RMVar_ID_90846 Human_SNP_ID_502289472 m1A Human chr12 - 55994215 55994215 55994215 TAAAAAGGATGCACTGGGTGCTATGGGGGGCCAGTGGCTTCTGGGAAAGGAAGGGGGAAATGTGT TAAAAAGGATGCACTGGGTGCTATGGGGGGCCGGTGGCTTCTGGGAAAGGAAGGGGGAAATGTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55994164..55994261 26863196 MeRIP-seq:(Medium) rs953720740 Functional Loss SNV dbSNP153 33..33 33 - - - 90847 RMVar_ID_90847 Human_SNP_ID_502289509 m1A Human chr12 - 55994385 55994385 55994385 AGGCCAAATCCTGTTCCTATGGGGGTGGGGGGAGGGAGAAGCCTGGGGAAGTGGTTTCCCAGGCC AGGCCAAATCCTGTTCCTATGGGGGTGGGGGGTGGGAGAAGCCTGGGGAAGTGGTTTCCCAGGCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55994337..55994487 32194978 MeRIP-seq:(Medium) rs1434479954 Functional Loss SNV dbSNP153 33..33 33 - - - 90848 RMVar_ID_90848 Human_SNP_ID_502289510 m1A Human chr12 - 55994385 55994385 55994385 AGGCCAAATCCTGTTCCTATGGGGGTGGGGGGAGGGAGAAGCCTGGGGAAGTGGTTTCCCAGGCC AGGCCAAATCCTGTTCCTATGGGGGTGGGGGGGGGGAGAAGCCTGGGGAAGTGGTTTCCCAGGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55994337..55994487 32194978 MeRIP-seq:(Medium) rs1434479954 Functional Loss SNV dbSNP153 33..33 33 - - - 90849 RMVar_ID_90849 Human_SNP_ID_502293361 m1A Human chr12 - 56007527 56007527 56007527 TCAGAGGCGGCGGTGGCGGCGGCTCCATCTCCATCAGCAGCTTCACCTGAGAAGGGACTTGCCCC TCAGAGGCGGCGGTGGCGGCGGCTCCATCTCCGTCAGCAGCTTCACCTGAGAAGGGACTTGCCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56007476..56007675 26863196 MeRIP-seq:(Medium) rs1195654058 Functional Loss SNV dbSNP153 33..33 33 - - - 90850 RMVar_ID_90850 Human_SNP_ID_502293365 m1A Human chr12 + 56007546 56007537 56007546 GTGAAGCTGCTGATGGAGATGGAGCCGCCGCCACCGCCGCCTCTGAGCGCCCGGGTCCTGGCTCC GTGAAGCTGCTGATGGAGATGGAG_________CCGCCGCCTCTGAGCGCCCGGGTCCTGGCTCC GCCGCCGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56007496..56007657 26863196 MeRIP-seq:(Medium) rs1230389288 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4231566 90851 RMVar_ID_90851 Human_SNP_ID_502294223 m1A Human chr12 - 56011379 56011379 56011379 GAAGAGAGAGAAGGCTAAGGTTTATGAGTGGGAGAAGAAACGATCCTATCCCTCCCATGTCTCAT GAAGAGAGAGAAGGCTAAGGTTTATGAGTGGGTGAAGAAACGATCCTATCCCTCCCATGTCTCAT T A LOC105369781 RNACentral:URS0000A76FC9 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56011374..56011516 26863196 MeRIP-seq:(Medium) rs922642933 Functional Loss SNV dbSNP153 33..33 33 - - - 90852 RMVar_ID_90852 Human_SNP_ID_502319503 m1A Human chr12 + 56104686 56104685 56104687 TCTGACCACAGCCTGTGGCTGGGAAGGGAGACAGAGGCGGCGGCGGCTCAGGGGAAACGAGGCTG TCTGACCACAGCCTGTGGCTGGGAAGGGAGAC__AGGCGGCGGCGGCTCAGGGGAAACGAGGCTG CAG C PA2G4,AC034102.2 Ensembl:ENSG00000170515,Ensembl:ENSG00000257411 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56104576..56104750 26863196 MeRIP-seq:(Medium) rs767837033 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_35399,Human_RBP_ID_754168,Human_RBP_ID_811294,Human_RBP_ID_4231632,Human_RBP_ID_5314585,Human_RBP_ID_5461956,Human_RBP_ID_5521549,Human_RBP_ID_8786744,Human_RBP_ID_8940713,Human_RBP_ID_9279002,Human_RBP_ID_9322554,Human_RBP_ID_22437140,Human_RBP_ID_26320924,Human_RBP_ID_26768395,Human_RBP_ID_26908943,Human_RBP_ID_27836760 Human_miRNA_ID_1973295,Human_miRNA_ID_1975471,Human_miRNA_ID_3010687 RMVar_hsa_circ_95145,RMVar_hsa_circ_157157 90853 RMVar_ID_90853 Human_SNP_ID_502319525 m1A Human chr12 - 56104722 56104722 56104722 TCGTCCTCGCCCGACATCTTCCTACTACCACCACTGCAGCCTCGTTTCCCCTGAGCCGCCGCCGC TCGTCCTCGCCCGACATCTTCCTACTACCACCGCTGCAGCCTCGTTTCCCCTGAGCCGCCGCCGC T C AC034102.4 Ensembl:ENSG00000257553 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:56104676..56104750 26863196 MeRIP-seq:(Medium) rs758771002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1381436 90854 RMVar_ID_90854 Human_SNP_ID_502319530 m1A Human chr12 - 56104741 56104741 56104741 GATAGTTTGCTCCTGTTGCTCGTCCTCGCCCGACATCTTCCTACTACCACCACTGCAGCCTCGTT GATAGTTTGCTCCTGTTGCTCGTCCTCGCCCGGCATCTTCCTACTACCACCACTGCAGCCTCGTT T C AC034102.4 Ensembl:ENSG00000257553 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:56104551..56105081;chr12:56104551..56104800 26863196 MeRIP-seq:(Medium) rs1359795464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1381436 90855 RMVar_ID_90855 Human_SNP_ID_502322742 m1A Human chr12 - 56116661 56116661 56116661 CGGAATCCCAACGCAGGAACCAAAAAACACTCACCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG CGGAATCCCAACGCAGGAACCAAAAAACACTCGCCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56116626..56116675 32194978 MeRIP-seq:(Medium) rs987428401 Functional Loss SNV dbSNP153 33..33 33 - - - 90856 RMVar_ID_90856 Human_SNP_ID_502322765 m1A Human chr12 - 56116679 56116679 56116679 ATGTCTATGGATTGTACACGGAATCCCAACGCAGGAACCAAAAAACACTCACCCAAAAAAATGGC ATGTCTATGGATTGTACACGGAATCCCAACGCTGGAACCAAAAAACACTCACCCAAAAAAATGGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:56116676..56117000 26863196 MeRIP-seq:(Medium) rs1388733444 Functional Loss SNV dbSNP153 33..33 33 - - - 90857 RMVar_ID_90857 Human_SNP_ID_502322823 m1A Human chr12 - 56116831 56116831 56116831 CTTCGTCTCCTCGCTACTACTCGCCAACTCCTACCTCCCAAGCTTACTACCAGGAACCGCTCACC CTTCGTCTCCTCGCTACTACTCGCCAACTCCTTCCTCCCAAGCTTACTACCAGGAACCGCTCACC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:56116691..56116922 26863196 MeRIP-seq:(Medium) rs1177895972 Functional Loss SNV dbSNP153 33..33 33 - - - 90858 RMVar_ID_90858 Human_SNP_ID_502322954 m1A Human chr12 - 56117178 56117178 56117178 TGCGCATTCGCTTCTTCCTCCACTAGCAACCGATCACAAGCAGCAGATAATTAAAAAAAAAAAAA TGCGCATTCGCTTCTTCCTCCACTAGCAACCGCTCACAAGCAGCAGATAATTAAAAAAAAAAAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:56117176..56117225 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1201799091 Functional Loss SNV dbSNP153 33..33 33 - - - 90859 RMVar_ID_90859 Human_SNP_ID_502322968 m1A Human chr12 + 56117210 56117210 56117210 TCGGTTGCTAGTGGAGGAAGAAGCGAATGCGCAGGTACGTTGAGACTTTGCCAGCCCAGGAGGAG TCGGTTGCTAGTGGAGGAAGAAGCGAATGCGCGGGTACGTTGAGACTTTGCCAGCCCAGGAGGAG A G RPL41 Ensembl:ENSG00000229117 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755027524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229524,Human_RBP_ID_754560,Human_RBP_ID_810592,Human_RBP_ID_876203,Human_RBP_ID_2345010,Human_RBP_ID_4246739,Human_RBP_ID_5111482,Human_RBP_ID_9365012,Human_RBP_ID_11985561,Human_RBP_ID_17650413,Human_RBP_ID_19058341,Human_RBP_ID_23566502,Human_RBP_ID_24543273 Human_Splice_Rec_1381440,Human_Splice_Rec_1381441,Human_Splice_Rec_1381446,Human_Splice_Rec_1381447,Human_Splice_Rec_1381452,Human_Splice_Rec_1381453,Human_Splice_Rec_1381456,Human_Splice_Rec_1381457,Human_Splice_Rec_1381461 RMVar_hsa_circ_100792,RMVar_hsa_circ_92885,RMVar_hsa_circ_157164,RMVar_hsa_circ_361198,RMVar_hsa_circ_124083,RMVar_hsa_circ_157165,RMVar_hsa_circ_157167 90860 RMVar_ID_90860 Human_SNP_ID_502322969 m1A Human chr12 + 56117210 56117210 56117210 TCGGTTGCTAGTGGAGGAAGAAGCGAATGCGCAGGTACGTTGAGACTTTGCCAGCCCAGGAGGAG TCGGTTGCTAGTGGAGGAAGAAGCGAATGCGCTGGTACGTTGAGACTTTGCCAGCCCAGGAGGAG A T RPL41 Ensembl:ENSG00000229117 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755027524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229524,Human_RBP_ID_754560,Human_RBP_ID_810592,Human_RBP_ID_876203,Human_RBP_ID_2345010,Human_RBP_ID_4246739,Human_RBP_ID_5111482,Human_RBP_ID_9365012,Human_RBP_ID_11985561,Human_RBP_ID_17650413,Human_RBP_ID_19058341,Human_RBP_ID_23566502,Human_RBP_ID_24543273 Human_Splice_Rec_1381440,Human_Splice_Rec_1381441,Human_Splice_Rec_1381446,Human_Splice_Rec_1381447,Human_Splice_Rec_1381452,Human_Splice_Rec_1381453,Human_Splice_Rec_1381456,Human_Splice_Rec_1381457,Human_Splice_Rec_1381461 RMVar_hsa_circ_100792,RMVar_hsa_circ_92885,RMVar_hsa_circ_157164,RMVar_hsa_circ_361198,RMVar_hsa_circ_124083,RMVar_hsa_circ_157165,RMVar_hsa_circ_157167 90861 RMVar_ID_90861 Human_SNP_ID_502324198 m1A Human chr12 + 56121537 56121537 56121537 ACTCTCAGCAGCCAGGCTCTACAGCCTCGTCCAGTGTCCCAGCAAGAACTGGTGGCCCCTGCTGG ACTCTCAGCAGCCAGGCTCTACAGCCTCGTCCCGTGTCCCAGCAAGAACTGGTGGCCCCTGCTGG A C ESYT1,ZC3H10 Ensembl:ENSG00000139641,Ensembl:ENSG00000135482 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56121529..56121611 26863196 MeRIP-seq:(Medium) rs775379613 Functional Loss SNV dbSNP153 33..33 33 - - - 90862 RMVar_ID_90862 Human_SNP_ID_502325864 m1A Human chr12 + 56128334 56128334 56128334 CCTCCCAGAGGTGGCACAATGGAGCGATCTCCAGGAGAGGGCCCCAGCCCCAGCCCCATGGACCA CCTCCCAGAGGTGGCACAATGGAGCGATCTCCTGGAGAGGGCCCCAGCCCCAGCCCCATGGACCA A T ESYT1 Ensembl:ENSG00000139641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56128285..56128389 26863196 MeRIP-seq:(Medium) rs775136500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423600,Human_RBP_ID_753828,Human_RBP_ID_4231776,Human_RBP_ID_9279003,Human_RBP_ID_18189160,Human_RBP_ID_18469177 Human_miRNA_ID_1984932,Human_miRNA_ID_2684941,Human_miRNA_ID_2940569 RMVar_hsa_circ_75843,RMVar_hsa_circ_110389,RMVar_hsa_circ_85928,RMVar_hsa_circ_157170,RMVar_hsa_circ_157171,RMVar_hsa_circ_157169 90863 RMVar_ID_90863 Human_SNP_ID_502325866 m1A Human chr12 + 56128347 56128341 56128347 GCACAATGGAGCGATCTCCAGGAGAGGGCCCCAGCCCCAGCCCCATGGACCAGCCCTCTGCTCCC GCACAATGGAGCGATCTCCAGGAGAGG______GCCCCAGCCCCATGGACCAGCCCTCTGCTCCC GGCCCCA G ESYT1 Ensembl:ENSG00000139641 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr12:56128296..56128425;chr12:56128296..56128382 26863196 MeRIP-seq:(Medium) rs750033680 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4246140,Human_RBP_ID_9279003,Human_RBP_ID_9322562,Human_RBP_ID_18469177 Human_miRNA_ID_2684941 RMVar_hsa_circ_75843,RMVar_hsa_circ_110389,RMVar_hsa_circ_85928,RMVar_hsa_circ_157170,RMVar_hsa_circ_157171,RMVar_hsa_circ_157169 90864 RMVar_ID_90864 Human_SNP_ID_502325873 m1A Human chr12 + 56128347 56128347 56128347 GCACAATGGAGCGATCTCCAGGAGAGGGCCCCAGCCCCAGCCCCATGGACCAGCCCTCTGCTCCC GCACAATGGAGCGATCTCCAGGAGAGGGCCCCTGCCCCAGCCCCATGGACCAGCCCTCTGCTCCC A T ESYT1 Ensembl:ENSG00000139641 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr12:56128296..56128425;chr12:56128296..56128382 26863196 MeRIP-seq:(Medium) rs1300590540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246140,Human_RBP_ID_9279003,Human_RBP_ID_9322562,Human_RBP_ID_18469177 Human_miRNA_ID_2684941 RMVar_hsa_circ_75843,RMVar_hsa_circ_110389,RMVar_hsa_circ_85928,RMVar_hsa_circ_157170,RMVar_hsa_circ_157171,RMVar_hsa_circ_157169 90865 RMVar_ID_90865 Human_SNP_ID_502326995 m1A Human chr12 - 56132259 56132259 56132259 CAGGCACAAGGGGCACCAGTAATCGGTTGGGCAACACGAGGAAGGCAGCAATGGAGTCCATGATC CAGGCACAAGGGGCACCAGTAATCGGTTGGGCGACACGAGGAAGGCAGCAATGGAGTCCATGATC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56132201..56132350 32194978 MeRIP-seq:(Medium) rs533020647 Functional Loss SNV dbSNP153 33..33 33 - - - 90866 RMVar_ID_90866 Human_SNP_ID_502327006 m1A Human chr12 - 56132274 56132274 56132274 CCACATCTTGAAGGTCAGGCACAAGGGGCACCAGTAATCGGTTGGGCAACACGAGGAAGGCAGCA CCACATCTTGAAGGTCAGGCACAAGGGGCACCTGTAATCGGTTGGGCAACACGAGGAAGGCAGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56132201..56132275 26863196 MeRIP-seq:(Medium) rs1246935136 Functional Loss SNV dbSNP153 33..33 33 - - - 90867 RMVar_ID_90867 Human_SNP_ID_502327192 m1A Human chr12 - 56132792 56132792 56132792 AATCCTAACAGGCAGAGTCTCACCTGCCCAGAAAGTCATCTTTATCTGGATCCTTGTCGAACACC AATCCTAACAGGCAGAGTCTCACCTGCCCAGAGAGTCATCTTTATCTGGATCCTTGTCGAACACC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56132701..56132825 32194978 MeRIP-seq:(Medium) rs1016782676 Functional Loss SNV dbSNP153 33..33 33 - - - 90868 RMVar_ID_90868 Human_SNP_ID_502327505 m1A Human chr12 - 56133847 56133847 56133847 ACTCACAGGAAGATCCTGGGCCCGATCCAGGTAGACAACTAAGATGGCAGCTGACGGGGGATCTG ACTCACAGGAAGATCCTGGGCCCGATCCAGGTGGACAACTAAGATGGCAGCTGACGGGGGATCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56133776..56133850 32194978 MeRIP-seq:(Medium) rs1177062772 Functional Loss SNV dbSNP153 33..33 33 - - - 90869 RMVar_ID_90869 Human_SNP_ID_502328803 m1A Human chr12 - 56138222 56138222 56138222 AGTGGGACGGGGGGTGAGACGCTCCAGGCGCAAGTGCAGGCGGCCAGATGGGACATCCTCCAGGG AGTGGGACGGGGGGTGAGACGCTCCAGGCGCAGGTGCAGGCGGCCAGATGGGACATCCTCCAGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56138201..56138225 26863196 MeRIP-seq:(Medium) rs1458151760 Functional Loss SNV dbSNP153 33..33 33 - - - 90870 RMVar_ID_90870 Human_SNP_ID_502328804 m1A Human chr12 - 56138222 56138222 56138222 AGTGGGACGGGGGGTGAGACGCTCCAGGCGCAAGTGCAGGCGGCCAGATGGGACATCCTCCAGGG AGTGGGACGGGGGGTGAGACGCTCCAGGCGCACGTGCAGGCGGCCAGATGGGACATCCTCCAGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56138201..56138225 26863196 MeRIP-seq:(Medium) rs1458151760 Functional Loss SNV dbSNP153 33..33 33 - - - 90871 RMVar_ID_90871 Human_SNP_ID_502329053 m1A Human chr12 + 56138930 56138930 56138930 TACTGATCATAAGCCCTCATCTCCACCAGACTATTTCGCAAACTTCAGCCCCTGTCTGGGATGAG TACTGATCATAAGCCCTCATCTCCACCAGACTGTTTCGCAAACTTCAGCCCCTGTCTGGGATGAG A G ESYT1 Ensembl:ENSG00000139641 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56138926..56139025 32194978 MeRIP-seq:(Medium) rs1354295577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22646521 Human_Splice_Rec_1381518,Human_Splice_Rec_1381519,Human_Splice_Rec_1381578,Human_Splice_Rec_1381579,Human_Splice_Rec_1381622,Human_Splice_Rec_1381623,Human_Splice_Rec_1381628,Human_Splice_Rec_1381629,Human_Splice_Rec_1381631 Human_miRNA_ID_2643753,Human_miRNA_ID_2643754 RMVar_hsa_circ_85928,RMVar_hsa_circ_95182,RMVar_hsa_circ_96582,RMVar_hsa_circ_157171,RMVar_hsa_circ_116888,RMVar_hsa_circ_157172,RMVar_hsa_circ_157174,RMVar_hsa_circ_105977,RMVar_hsa_circ_157175,RMVar_hsa_circ_126519,RMVar_hsa_circ_157179,RMVar_hsa_circ_39757,RMVar_hsa_circ_157182,RMVar_hsa_circ_87083,RMVar_hsa_circ_373168,RMVar_hsa_circ_157183,RMVar_hsa_circ_157184,RMVar_hsa_circ_75755,RMVar_hsa_circ_157187,RMVar_hsa_circ_121701,RMVar_hsa_circ_92390,RMVar_hsa_circ_157188,RMVar_hsa_circ_157189,RMVar_hsa_circ_101332,RMVar_hsa_circ_157193,RMVar_hsa_circ_157195,RMVar_hsa_circ_119482,RMVar_hsa_circ_85721,RMVar_hsa_circ_157197,RMVar_hsa_circ_43178,RMVar_hsa_circ_108033,RMVar_hsa_circ_89473,RMVar_hsa_circ_157198,RMVar_hsa_circ_92717,RMVar_hsa_circ_157201,RMVar_hsa_circ_80348,RMVar_hsa_circ_157200,RMVar_hsa_circ_329086,RMVar_hsa_circ_101760,RMVar_hsa_circ_157203,RMVar_hsa_circ_157204,RMVar_hsa_circ_157206,RMVar_hsa_circ_21821,RMVar_hsa_circ_81613,RMVar_hsa_circ_110669,RMVar_hsa_circ_91314,RMVar_hsa_circ_324796,RMVar_hsa_circ_157208,RMVar_hsa_circ_101024,RMVar_hsa_circ_100724,RMVar_hsa_circ_157210,RMVar_hsa_circ_157211,RMVar_hsa_circ_157209,RMVar_hsa_circ_157213,RMVar_hsa_circ_90125,RMVar_hsa_circ_106615,RMVar_hsa_circ_157214,RMVar_hsa_circ_157215 90872 RMVar_ID_90872 Human_SNP_ID_502333424 m1A Human chr12 + 56153932 56153932 56153932 CCTTTGGCCACCGGACATCATGCCTCCCAAGAAGGATGTTCCCGTGAAGAAACCAGCAGGGCCCT CCTTTGGCCACCGGACATCATGCCTCCCAAGACGGATGTTCCCGTGAAGAAACCAGCAGGGCCCT A C MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:56153831..56153973 26863410 MeRIP-seq:(Medium) rs748463155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876930,Human_RBP_ID_4246744,Human_RBP_ID_5111486,Human_RBP_ID_9322566,Human_RBP_ID_17650736,Human_RBP_ID_18188823,Human_RBP_ID_18629541,Human_RBP_ID_18975731,Human_RBP_ID_23566550,Human_RBP_ID_26909034 Human_Splice_Rec_1381670,Human_Splice_Rec_1381698,Human_Splice_Rec_1381706 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221 90873 RMVar_ID_90873 Human_SNP_ID_502333635 m1A Human chr12 + 56154832 56154832 56154832 TTTTCTTCCACAGATCGAGTTTAACAAGGACCAGCTGGAGGGTGAGGAGAAGCTCATCTAAGGCC TTTTCTTCCACAGATCGAGTTTAACAAGGACCTGCTGGAGGGTGAGGAGAAGCTCATCTAAGGCC A T MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56153849..56154867 32194978 MeRIP-seq:(Medium) rs142239260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876932 Human_Splice_Rec_1381672,Human_Splice_Rec_1381673,Human_Splice_Rec_1381684,Human_Splice_Rec_1381685,Human_Splice_Rec_1381700,Human_Splice_Rec_1381701,Human_Splice_Rec_1381708,Human_Splice_Rec_1381709,Human_Splice_Rec_1381718,Human_Splice_Rec_1381719,Human_Splice_Rec_1381726 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221 90874 RMVar_ID_90874 Human_SNP_ID_502333736 m1A Human chr12 + 56155156 56155156 56155156 ACGTGATGAGGGCCCTGGGCCAGAACCCCACCAACGCCGAGGTGCTCAAGGTCCTGGGGAACCCC ACGTGATGAGGGCCCTGGGCCAGAACCCCACCGACGCCGAGGTGCTCAAGGTCCTGGGGAACCCC A G MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56155105..56155231 26863196 MeRIP-seq:(Medium) rs1352842372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229462,Human_RBP_ID_423649,Human_RBP_ID_3941755,Human_RBP_ID_5111487,Human_RBP_ID_17822901,Human_RBP_ID_18977301 Human_Splice_Rec_1381675,Human_Splice_Rec_1381687,Human_Splice_Rec_1381703,Human_Splice_Rec_1381711,Human_Splice_Rec_1381721,Human_Splice_Rec_1381727 Human_miRNA_ID_2017868 RMVar_hsa_circ_104306,RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221,RMVar_hsa_circ_157222,RMVar_hsa_circ_157223 90875 RMVar_ID_90875 Human_SNP_ID_502333755 m1A Human chr12 + 56155189 56155188 56155190 ACGCCGAGGTGCTCAAGGTCCTGGGGAACCCCAAGAGTGATGGTGAGGGGACCCTTGGGAACAAT ACGCCGAGGTGCTCAAGGTCCTGGGGAACCCC__GAGTGATGGTGAGGGGACCCTTGGGAACAAT CAA C MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56155051..56155630 32194978 MeRIP-seq:(Medium) rs779894173 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_229462,Human_RBP_ID_423649,Human_RBP_ID_18977301,Human_RBP_ID_19058353 Human_Splice_Rec_1381675,Human_Splice_Rec_1381687,Human_Splice_Rec_1381703,Human_Splice_Rec_1381711,Human_Splice_Rec_1381721,Human_Splice_Rec_1381727 RMVar_hsa_circ_104306,RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221,RMVar_hsa_circ_157222,RMVar_hsa_circ_157223 90876 RMVar_ID_90876 Human_SNP_ID_502334423 m1A Human chr12 - 56157454 56157454 56157454 TCCTCAGTCATCTTCTCTCCTGAATCCCAGACACAACGTCTGAGGCCCTCCTTTCCCTCCTTCAC TCCTCAGTCATCTTCTCTCCTGAATCCCAGACCCAACGTCTGAGGCCCTCCTTTCCCTCCTTCAC T G AC034102.5 Ensembl:ENSG00000257809 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56157451..56157550 32194978 MeRIP-seq:(Medium) rs1565882021 Functional Loss SNV dbSNP153 33..33 33 - - - 90877 RMVar_ID_90877 Human_SNP_ID_502334447 m1A Human chr12 + 56157516 56157516 56157516 GGAGGAGGTGGAGACCGTTCTGGCAGGACACGAGGACAGCAACGGCTGCATCAACTACGAGGGTG GGAGGAGGTGGAGACCGTTCTGGCAGGACACGCGGACAGCAACGGCTGCATCAACTACGAGGGTG A C MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56157359..56157580 26863196 MeRIP-seq:(Medium) rs1220331891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423659,Human_RBP_ID_810815,Human_RBP_ID_876937,Human_RBP_ID_5111979,Human_RBP_ID_5555496,Human_RBP_ID_17684895 Human_Splice_Rec_1381678,Human_Splice_Rec_1381679,Human_Splice_Rec_1381690,Human_Splice_Rec_1381691,Human_Splice_Rec_1381713,Human_Splice_Rec_1381730,Human_Splice_Rec_1381731,Human_Splice_Rec_1381735,Human_Splice_Rec_1381737,Human_Splice_Rec_1381741 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224 90878 RMVar_ID_90878 Human_SNP_ID_502334449 m1A Human chr12 + 56157519 56157519 56157519 GGAGGTGGAGACCGTTCTGGCAGGACACGAGGACAGCAACGGCTGCATCAACTACGAGGGTGAGG GGAGGTGGAGACCGTTCTGGCAGGACACGAGGGCAGCAACGGCTGCATCAACTACGAGGGTGAGG A G MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:56157409..56157582;chr12:56157359..56157627 26863196 MeRIP-seq:(Medium) rs773304984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423659,Human_RBP_ID_810815,Human_RBP_ID_876937,Human_RBP_ID_5111979,Human_RBP_ID_17684896 Human_Splice_Rec_1381678,Human_Splice_Rec_1381679,Human_Splice_Rec_1381690,Human_Splice_Rec_1381691,Human_Splice_Rec_1381713,Human_Splice_Rec_1381730,Human_Splice_Rec_1381731,Human_Splice_Rec_1381735,Human_Splice_Rec_1381737,Human_Splice_Rec_1381741 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224 90879 RMVar_ID_90879 Human_SNP_ID_502334853 m1A Human chr12 + 56158402 56158402 56158402 AGGAAAAGGTCCCGGAGAGCTGAGCAGTCAAGATGGTGGGGCCCAGGTCTTGGGAGACGGGCAGG AGGAAAAGGTCCCGGAGAGCTGAGCAGTCAAGTTGGTGGGGCCCAGGTCTTGGGAGACGGGCAGG A T MYL6,MYL6B Ensembl:ENSG00000092841,Ensembl:ENSG00000196465 Protein coding,Protein coding start codon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:56158376..56158450 26863196 MeRIP-seq:(Medium) rs1214516266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753139,Human_RBP_ID_811676,Human_RBP_ID_3943054,Human_RBP_ID_4246745,Human_RBP_ID_5111756,Human_RBP_ID_5139637,Human_RBP_ID_5314586,Human_RBP_ID_5462322,Human_RBP_ID_11985823,Human_RBP_ID_22426162,Human_RBP_ID_22435959,Human_RBP_ID_23208114 Human_Splice_Rec_1381749,Human_Splice_Rec_1381757,Human_Splice_Rec_1381767,Human_Splice_Rec_1381775,Human_Splice_Rec_1381785,Human_Splice_Rec_1381797,Human_Splice_Rec_1381807,Human_Splice_Rec_1381819,Human_Splice_Rec_1381837,Human_Splice_Rec_1381847,Human_Splice_Rec_1381853,Human_Splice_Rec_1381865,Human_Splice_Rec_1381873,Human_Splice_Rec_1381883,Human_Splice_Rec_1381891,Human_Splice_Rec_1381903 Human_miRNA_ID_2295694,Human_miRNA_ID_2295695 RMVar_hsa_circ_84206,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224,RMVar_hsa_circ_112837,RMVar_hsa_circ_157226,RMVar_hsa_circ_157227 90880 RMVar_ID_90880 Human_SNP_ID_502334854 m1A Human chr12 - 56158406 56158406 56158406 CAATCCTGCCCGTCTCCCAAGACCTGGGCCCCACCATCTTGACTGCTCAGCTCTCCGGGACCTTT CAATCCTGCCCGTCTCCCAAGACCTGGGCCCCCCCATCTTGACTGCTCAGCTCTCCGGGACCTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56158326..56158812 26863196 MeRIP-seq:(Medium) rs111759183 Functional Loss SNV dbSNP153 33..33 33 - - - 90881 RMVar_ID_90881 Human_SNP_ID_502335292 m1A Human chr12 + 56159579 56159579 56159579 AACCCTCAAATCCTGTGTTGACATTCATCTGAATCCTCAGAGTTCAAGGAGGCCTTCCAGCTGTT AACCCTCAAATCCTGTGTTGACATTCATCTGATTCCTCAGAGTTCAAGGAGGCCTTCCAGCTGTT A T MYL6,MYL6B Ensembl:ENSG00000092841,Ensembl:ENSG00000196465 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56159576..56159600 26863196 MeRIP-seq:(Medium) rs1380056233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_873688,Human_RBP_ID_22646530 Human_Splice_Rec_1381770,Human_Splice_Rec_1381771,Human_Splice_Rec_1381801,Human_Splice_Rec_1381895 Human_miRNA_ID_3103531,Human_miRNA_ID_3103532 RMVar_hsa_circ_84206,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224,RMVar_hsa_circ_112837,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_157227,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_88064,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_157232 90882 RMVar_ID_90882 Human_SNP_ID_502335326 m1A Human chr12 - 56159671 56159671 56159671 TGAGCACCTCGGCGTTGGTAGGGTTCTGGCCCAGGGCCCTCATCACATCCCCACACTGGCTGTAC TGAGCACCTCGGCGTTGGTAGGGTTCTGGCCCGGGGCCCTCATCACATCCCCACACTGGCTGTAC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:56159626..56159675 26863196 MeRIP-seq:(Medium) rs1323853526 Functional Loss SNV dbSNP153 33..33 33 - - - 90883 RMVar_ID_90883 Human_SNP_ID_502335536 m1A Human chr12 + 56160261 56160259 56160262 CTTTCCCCCTGCAGGTGAGAAGATGACAGAGGAAGAAGTAGAGATGCTGGTGGCAGGGCATGAGG CTTTCCCCCTGCAGGTGAGAAGATGACAGAG___GAAGTAGAGATGCTGGTGGCAGGGCATGAGG GGAA G MYL6 Ensembl:ENSG00000092841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56159945..56160372 26863196 MeRIP-seq:(Medium) rs774256464 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_423676,Human_RBP_ID_811764,Human_RBP_ID_874684,Human_RBP_ID_1474274,Human_RBP_ID_1797571,Human_RBP_ID_4231970,Human_RBP_ID_5111489,Human_RBP_ID_5139876,Human_RBP_ID_5346699,Human_RBP_ID_8379819,Human_RBP_ID_11985850,Human_RBP_ID_17649998,Human_RBP_ID_18977304,Human_RBP_ID_19703584,Human_RBP_ID_22040610,Human_RBP_ID_22435965,Human_RBP_ID_22574677,Human_RBP_ID_22755995,Human_RBP_ID_22905991,Human_RBP_ID_23113332,Human_RBP_ID_23207697,Human_RBP_ID_23566578,Human_RBP_ID_26322946,Human_RBP_ID_26418014,Human_RBP_ID_27423520,Human_RBP_ID_27805510 Human_Splice_Rec_1381754,Human_Splice_Rec_1381755,Human_Splice_Rec_1381762,Human_Splice_Rec_1381763,Human_Splice_Rec_1381774,Human_Splice_Rec_1381782,Human_Splice_Rec_1381783,Human_Splice_Rec_1381792,Human_Splice_Rec_1381793,Human_Splice_Rec_1381804,Human_Splice_Rec_1381805,Human_Splice_Rec_1381812,Human_Splice_Rec_1381816,Human_Splice_Rec_1381817,Human_Splice_Rec_1381826,Human_Splice_Rec_1381827,Human_Splice_Rec_1381836,Human_Splice_Rec_1381844,Human_Splice_Rec_1381845,Human_Splice_Rec_1381860,Human_Splice_Rec_1381861,Human_Splice_Rec_1381872,Human_Splice_Rec_1381890,Human_Splice_Rec_1381898,Human_Splice_Rec_1381899,Human_Splice_Rec_1381910,Human_Splice_Rec_1381911,Human_Splice_Rec_1381914,Human_Splice_Rec_1381915 Human_miRNA_ID_2441626 RMVar_hsa_circ_84206,RMVar_hsa_circ_81881,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_325389,RMVar_hsa_circ_36110,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235,RMVar_hsa_circ_126953,RMVar_hsa_circ_98857,RMVar_hsa_circ_157236,RMVar_hsa_circ_157237 90884 RMVar_ID_90884 Human_SNP_ID_502335539 m1A Human chr12 + 56160261 56160261 56160261 CTTTCCCCCTGCAGGTGAGAAGATGACAGAGGAAGAAGTAGAGATGCTGGTGGCAGGGCATGAGG CTTTCCCCCTGCAGGTGAGAAGATGACAGAGGGAGAAGTAGAGATGCTGGTGGCAGGGCATGAGG A G MYL6 Ensembl:ENSG00000092841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56159945..56160372 26863196 MeRIP-seq:(Medium) rs981911509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423676,Human_RBP_ID_811764,Human_RBP_ID_874684,Human_RBP_ID_1474274,Human_RBP_ID_1797571,Human_RBP_ID_4231970,Human_RBP_ID_5111489,Human_RBP_ID_5139876,Human_RBP_ID_5346699,Human_RBP_ID_8379819,Human_RBP_ID_11985850,Human_RBP_ID_17649998,Human_RBP_ID_18977304,Human_RBP_ID_19703584,Human_RBP_ID_22040610,Human_RBP_ID_22435965,Human_RBP_ID_22574677,Human_RBP_ID_22755995,Human_RBP_ID_22905991,Human_RBP_ID_23113332,Human_RBP_ID_23207697,Human_RBP_ID_23566578,Human_RBP_ID_26322946,Human_RBP_ID_26418014,Human_RBP_ID_27423520,Human_RBP_ID_27805510 Human_Splice_Rec_1381754,Human_Splice_Rec_1381755,Human_Splice_Rec_1381762,Human_Splice_Rec_1381763,Human_Splice_Rec_1381774,Human_Splice_Rec_1381782,Human_Splice_Rec_1381783,Human_Splice_Rec_1381792,Human_Splice_Rec_1381793,Human_Splice_Rec_1381804,Human_Splice_Rec_1381805,Human_Splice_Rec_1381812,Human_Splice_Rec_1381816,Human_Splice_Rec_1381817,Human_Splice_Rec_1381826,Human_Splice_Rec_1381827,Human_Splice_Rec_1381836,Human_Splice_Rec_1381844,Human_Splice_Rec_1381845,Human_Splice_Rec_1381860,Human_Splice_Rec_1381861,Human_Splice_Rec_1381872,Human_Splice_Rec_1381890,Human_Splice_Rec_1381898,Human_Splice_Rec_1381899,Human_Splice_Rec_1381910,Human_Splice_Rec_1381911,Human_Splice_Rec_1381914,Human_Splice_Rec_1381915 Human_miRNA_ID_2441626 RMVar_hsa_circ_84206,RMVar_hsa_circ_81881,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_325389,RMVar_hsa_circ_36110,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235,RMVar_hsa_circ_126953,RMVar_hsa_circ_98857,RMVar_hsa_circ_157236,RMVar_hsa_circ_157237 90885 RMVar_ID_90885 Human_SNP_ID_502335686 m1A Human chr12 - 56160641 56160641 56160641 TACCCGCCCCATGGGCCCGTCACCCCGACAGGATATGCCTCACAAACGCTGCAGGAAGGAAGAGA TACCCGCCCCATGGGCCCGTCACCCCGACAGGGTATGCCTCACAAACGCTGCAGGAAGGAAGAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56160637..56160837 32194978 MeRIP-seq:(Medium) rs767980073 Functional Loss SNV dbSNP153 33..33 33 - - - 90886 RMVar_ID_90886 Human_SNP_ID_502335687 m1A Human chr12 - 56160641 56160641 56160641 TACCCGCCCCATGGGCCCGTCACCCCGACAGGATATGCCTCACAAACGCTGCAGGAAGGAAGAGA TACCCGCCCCATGGGCCCGTCACCCCGACAGGCTATGCCTCACAAACGCTGCAGGAAGGAAGAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56160637..56160837 32194978 MeRIP-seq:(Medium) rs767980073 Functional Loss SNV dbSNP153 33..33 33 - - - 90887 RMVar_ID_90887 Human_SNP_ID_502336474 m1A Human chr12 - 56163431 56163431 56163431 AGAGGATAGGATGGGAATGCTGCCCTAAAGGAAGGGCTGGTGAAAGGTGTTTATACAAGGTTCTA AGAGGATAGGATGGGAATGCTGCCCTAAAGGACGGGCTGGTGAAAGGTGTTTATACAAGGTTCTA T G AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56163380..56163496 32194978 MeRIP-seq:(Medium) rs1247523377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810261,Human_RBP_ID_2345071,Human_RBP_ID_3421863,Human_RBP_ID_4248506,Human_RBP_ID_5557998,Human_RBP_ID_18262110,Human_RBP_ID_18629569,Human_RBP_ID_23566614,Human_RBP_ID_24365617 Human_miRNA_ID_175204,Human_miRNA_ID_176871 90888 RMVar_ID_90888 Human_SNP_ID_502336522 m1A Human chr12 + 56163655 56163654 56163655 GGAAGGGCTGTTCCTGGAACCGTGATGTCCACAGGGGGTGAGGGGGAGAGATGTCTGGCTGGCTC GGAAGGGCTGTTCCTGGAACCGTGATGTCCAC_GGGGGTGAGGGGGAGAGATGTCTGGCTGGCTC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56163605..56163786 26863196 MeRIP-seq:(Medium) rs1466522448 Functional Loss DEL dbSNP153 33..33 33 - - - 90889 RMVar_ID_90889 Human_SNP_ID_502336526 m1A Human chr12 + 56163655 56163655 56163655 GGAAGGGCTGTTCCTGGAACCGTGATGTCCACAGGGGGTGAGGGGGAGAGATGTCTGGCTGGCTC GGAAGGGCTGTTCCTGGAACCGTGATGTCCACCGGGGGTGAGGGGGAGAGATGTCTGGCTGGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56163605..56163786 26863196 MeRIP-seq:(Medium) rs1175672337 Functional Loss SNV dbSNP153 33..33 33 - - - 90890 RMVar_ID_90890 Human_SNP_ID_502336540 m1A Human chr12 + 56163673 56163673 56163673 ACCGTGATGTCCACAGGGGGTGAGGGGGAGAGATGTCTGGCTGGCTCCTCACTGTGGAGGTGGCA ACCGTGATGTCCACAGGGGGTGAGGGGGAGAGTTGTCTGGCTGGCTCCTCACTGTGGAGGTGGCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56163601..56163725 26863196 MeRIP-seq:(Medium) rs200882293 Functional Loss SNV dbSNP153 33..33 33 - - - 90891 RMVar_ID_90891 Human_SNP_ID_502336765 m1A Human chr12 - 56164450 56164450 56164450 TCCCCCCACCTAACCTGCCTGTGTCCATGGCGAACCCTCTACATCCTAACCTGCCGGCGACCACC TCCCCCCACCTAACCTGCCTGTGTCCATGGCGGACCCTCTACATCCTAACCTGCCGGCGACCACC T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56164401..56164623 26863196 MeRIP-seq:(Medium) rs781152017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3421335,Human_RBP_ID_5094342,Human_RBP_ID_5127149,Human_RBP_ID_5645307,Human_RBP_ID_9365021,Human_RBP_ID_17074854,Human_RBP_ID_17239611,Human_RBP_ID_17355294,Human_RBP_ID_17472478,Human_RBP_ID_21918856,Human_RBP_ID_21967069,Human_RBP_ID_22906018,Human_RBP_ID_26805800,Human_RBP_ID_27423539,Human_RBP_ID_27558133 RMVar_hsa_circ_269519 90892 RMVar_ID_90892 Human_SNP_ID_502336786 m1A Human chr12 + 56164482 56164482 56164482 TCGCCATGGACACAGGCAGGTTAGGTGGGGGGAGAGTGCCCGGGGCGAACGGGAGATGGTGGTGA TCGCCATGGACACAGGCAGGTTAGGTGGGGGGGGAGTGCCCGGGGCGAACGGGAGATGGTGGTGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:56164451..56164700 26863196 MeRIP-seq:(Medium) rs752904444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120466,RMVar_hsa_circ_157241 90893 RMVar_ID_90893 Human_SNP_ID_502337043 m1A Human chr12 - 56165320 56165320 56165320 AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCATGGTAAGTGTTATGTTCCAGAACTTTTGTTGG AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCGTGGTAAGTGTTATGTTCCAGAACTTTTGTTGG T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56165316..56165394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_19058365 Human_Splice_Rec_1381975,Human_Splice_Rec_1382031,Human_Splice_Rec_1382089,Human_Splice_Rec_1382145,Human_Splice_Rec_1382199 RMVar_hsa_circ_35361,RMVar_hsa_circ_45211 90894 RMVar_ID_90894 Human_SNP_ID_502337044 m1A Human chr12 - 56165320 56165320 56165320 AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCATGGTAAGTGTTATGTTCCAGAACTTTTGTTGG AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCCTGGTAAGTGTTATGTTCCAGAACTTTTGTTGG T G AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56165316..56165394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_19058365 Human_Splice_Rec_1381975,Human_Splice_Rec_1382031,Human_Splice_Rec_1382089,Human_Splice_Rec_1382145,Human_Splice_Rec_1382199 RMVar_hsa_circ_35361,RMVar_hsa_circ_45211 90895 RMVar_ID_90895 Human_SNP_ID_502338442 m1A Human chr12 - 56169831 56169831 56169831 ACCAGCGAGGCTCCCAAGAAGGATGAGGAGAAAGGGAAAGAAGGCGACAGTGAGAAGGAGTCCGA ACCAGCGAGGCTCCCAAGAAGGATGAGGAGAAGGGGAAAGAAGGCGACAGTGAGAAGGAGTCCGA T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56162492..56190284 26863196 MeRIP-seq:(Medium) rs999428845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36191,Human_RBP_ID_195689,Human_RBP_ID_229564,Human_RBP_ID_2345075,Human_RBP_ID_3421342,Human_RBP_ID_5094347,Human_RBP_ID_5173646,Human_RBP_ID_5558009,Human_RBP_ID_6240777,Human_RBP_ID_8179235,Human_RBP_ID_9279025,Human_RBP_ID_9365027,Human_RBP_ID_18977311,Human_RBP_ID_26321535,Human_RBP_ID_26422368,Human_RBP_ID_27805514 Human_Splice_Rec_1381968,Human_Splice_Rec_1381969,Human_Splice_Rec_1382024,Human_Splice_Rec_1382025,Human_Splice_Rec_1382082,Human_Splice_Rec_1382083,Human_Splice_Rec_1382138,Human_Splice_Rec_1382139,Human_Splice_Rec_1382192,Human_Splice_Rec_1382193 RMVar_hsa_circ_35361,RMVar_hsa_circ_301177,RMVar_hsa_circ_346506,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882,RMVar_hsa_circ_341930,RMVar_hsa_circ_157242 90896 RMVar_ID_90896 Human_SNP_ID_502338465 m1A Human chr12 - 56169903 56169903 56169903 CCTTTTCTATCACTGGAATTTCAGGAACCCCGAGAAGGAGGGGGTGCTATAGAGGAGGAAGCAAA CCTTTTCTATCACTGGAATTTCAGGAACCCCGGGAAGGAGGGGGTGCTATAGAGGAGGAAGCAAA T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:56169776..56169925 26863196 MeRIP-seq:(Medium) rs750399849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229564,Human_RBP_ID_5094347,Human_RBP_ID_5558009,Human_RBP_ID_6240777,Human_RBP_ID_23207704,Human_RBP_ID_26321537,Human_RBP_ID_27805515 Human_Splice_Rec_1381968,Human_Splice_Rec_1382024,Human_Splice_Rec_1382082,Human_Splice_Rec_1382138,Human_Splice_Rec_1382192 RMVar_hsa_circ_35361,RMVar_hsa_circ_301177,RMVar_hsa_circ_346506,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882,RMVar_hsa_circ_341930,RMVar_hsa_circ_157242 90897 RMVar_ID_90897 Human_SNP_ID_502338549 m1A Human chr12 - 56170154 56170152 56170155 TCGGGTGGAAGGCCAGGCCACAGATGAGAAGAAGGAGCCCAAGGTATAGAGGGATTTCTGGAAGC TCGGGTGGAAGGCCAGGCCACAGATGAGAAG___GAGCCCAAGGTATAGAGGGATTTCTGGAAGC CCTT C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:56170126..56170225;chr12:56169601..56170283 26863196 MeRIP-seq:(Medium) rs368938279 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_228273,Human_RBP_ID_260080,Human_RBP_ID_3941762,Human_RBP_ID_5521551,Human_RBP_ID_5558011,Human_RBP_ID_6240777,Human_RBP_ID_9279671,Human_RBP_ID_18977312,Human_RBP_ID_22910751,Human_RBP_ID_24543071,Human_RBP_ID_26321538 Human_Splice_Rec_1381966,Human_Splice_Rec_1381967,Human_Splice_Rec_1382022,Human_Splice_Rec_1382023,Human_Splice_Rec_1382080,Human_Splice_Rec_1382081,Human_Splice_Rec_1382136,Human_Splice_Rec_1382137,Human_Splice_Rec_1382190,Human_Splice_Rec_1382191 RMVar_hsa_circ_35361,RMVar_hsa_circ_116143,RMVar_hsa_circ_301177,RMVar_hsa_circ_346506,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882,RMVar_hsa_circ_341930,RMVar_hsa_circ_157242,RMVar_hsa_circ_157243 90898 RMVar_ID_90898 Human_SNP_ID_502338866 m1A Human chr12 + 56171220 56171220 56171220 ACTTGAGGCAGAAATGGCACAGGAGGCCAGGTAGCTCTGGATCTTGTGAAAGGCAAGAAATCTGG ACTTGAGGCAGAAATGGCACAGGAGGCCAGGTGGCTCTGGATCTTGTGAAAGGCAAGAAATCTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56171215..56171400 26863196 MeRIP-seq:(Medium) rs762677068 Functional Loss SNV dbSNP153 33..33 33 - - - 90899 RMVar_ID_90899 Human_SNP_ID_502340790 m1A Human chr12 - 56178506 56178506 56178506 GTAGGATGAGGATGAGAACAGTACGGGGAACAAGGGAGAGCAGACCAAGAATCCAGACCTGCATG GTAGGATGAGGATGAGAACAGTACGGGGAACATGGGAGAGCAGACCAAGAATCCAGACCTGCATG T A AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56162256..56190239 32194978 MeRIP-seq:(Medium) rs770505656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752496,Human_RBP_ID_809828,Human_RBP_ID_874691,Human_RBP_ID_1082419,Human_RBP_ID_1127918,Human_RBP_ID_1479668,Human_RBP_ID_3421875,Human_RBP_ID_5094358,Human_RBP_ID_5558030,Human_RBP_ID_6243592,Human_RBP_ID_8787246,Human_RBP_ID_9365034,Human_RBP_ID_17472481,Human_RBP_ID_18410863,Human_RBP_ID_18629586,Human_RBP_ID_22435971,Human_RBP_ID_22736915,Human_RBP_ID_24543072,Human_RBP_ID_26320928,Human_RBP_ID_27806684 Human_Splice_Rec_1381948,Human_Splice_Rec_1382004,Human_Splice_Rec_1382062,Human_Splice_Rec_1382118,Human_Splice_Rec_1382174 Human_miRNA_ID_1132334,Human_miRNA_ID_1546019 RMVar_hsa_circ_22335,RMVar_hsa_circ_35361,RMVar_hsa_circ_59915,RMVar_hsa_circ_116143,RMVar_hsa_circ_341930,RMVar_hsa_circ_157243,RMVar_hsa_circ_62147,RMVar_hsa_circ_90693,RMVar_hsa_circ_124352,RMVar_hsa_circ_121536,RMVar_hsa_circ_87782,RMVar_hsa_circ_157248,RMVar_hsa_circ_157249,RMVar_hsa_circ_157250,RMVar_hsa_circ_157247,RMVar_hsa_circ_67512,RMVar_hsa_circ_81197,RMVar_hsa_circ_157251,RMVar_hsa_circ_374858,RMVar_hsa_circ_24525,RMVar_hsa_circ_157253 90900 RMVar_ID_90900 Human_SNP_ID_502343877 m1A Human chr12 - 56189446 56189443 56189446 GGCCCGAGCCGGAGAAGATGGCGGTGCGGAAGAAGGACGGCGGCCCCAACGTGAAGTACTACGAG GGCCCGAGCCGGAGAAGATGGCGGTGCGGAAG___GACGGCGGCCCCAACGTGAAGTACTACGAG CCTT C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr12:56189351..56189600;chr12:56189351..56189595;chr12:56189367..56189507 26863196 MeRIP-seq:(Medium) rs759489434 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_228285,Human_RBP_ID_752566,Human_RBP_ID_1479831,Human_RBP_ID_3421358,Human_RBP_ID_3943073,Human_RBP_ID_4246748,Human_RBP_ID_5094371,Human_RBP_ID_5173678,Human_RBP_ID_5349698,Human_RBP_ID_5462426,Human_RBP_ID_5558037,Human_RBP_ID_5645321,Human_RBP_ID_8229886,Human_RBP_ID_8787247,Human_RBP_ID_9323134,Human_RBP_ID_9365051,Human_RBP_ID_22472004,Human_RBP_ID_24543077,Human_RBP_ID_26320929,Human_RBP_ID_27805533 Human_Splice_Rec_1381923,Human_Splice_Rec_1381979,Human_Splice_Rec_1382037,Human_Splice_Rec_1382093,Human_Splice_Rec_1382149,Human_Splice_Rec_1382249,Human_Splice_Rec_1382263,Human_Splice_Rec_1382277,Human_Splice_Rec_1382285 RMVar_hsa_circ_87782,RMVar_hsa_circ_157250,RMVar_hsa_circ_91631,RMVar_hsa_circ_157257 90901 RMVar_ID_90901 Human_SNP_ID_502343933 m1A Human chr12 - 56189550 56189550 56189550 AGGCGGCGGGAGGCGGCGGCCGCGGCGGCGGGAGGCGGCGGGAGGCGGGCGGAGGAGGAGGCGGA AGGCGGCGGGAGGCGGCGGCCGCGGCGGCGGGTGGCGGCGGGAGGCGGGCGGAGGAGGAGGCGGA T A AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:56189470..56189557 26863410 MeRIP-seq:(Medium) rs1209968542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87782,RMVar_hsa_circ_157250,RMVar_hsa_circ_91631,RMVar_hsa_circ_157257 90902 RMVar_ID_90902 Human_SNP_ID_502349913 m1A Human chr12 - 56213123 56213123 56213123 TGGGATCTACTGAAAAGACCAGCTTTTGATACAGCCATGCACTCTGCATTTTGATGTGAAAGCTG TGGGATCTACTGAAAAGACCAGCTTTTGATACGGCCATGCACTCTGCATTTTGATGTGAAAGCTG T C RNF41 Ensembl:ENSG00000181852 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56213121..56214041 32194978 MeRIP-seq:(Medium) rs1469619691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1382318,Human_Splice_Rec_1382332,Human_Splice_Rec_1382396 RMVar_hsa_circ_157261,RMVar_hsa_circ_85824,RMVar_hsa_circ_295183,RMVar_hsa_circ_347915,RMVar_hsa_circ_157262,RMVar_hsa_circ_157263 90903 RMVar_ID_90903 Human_SNP_ID_502352875 m1A Human chr12 - 56224434 56224434 56224434 CCCCTACCCGCAGCCCACCACCCACCCAAGCCAGCCGGCAGGACTGTGCACGCCGCTGAGCAGCC CCCCTACCCGCAGCCCACCACCCACCCAAGCCGGCCGGCAGGACTGTGCACGCCGCTGAGCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56224384..56224514 26863196 MeRIP-seq:(Medium) rs961353894 Functional Loss SNV dbSNP153 33..33 33 - - - 90904 RMVar_ID_90904 Human_SNP_ID_502352876 m1A Human chr12 - 56224434 56224434 56224434 CCCCTACCCGCAGCCCACCACCCACCCAAGCCAGCCGGCAGGACTGTGCACGCCGCTGAGCAGCC CCCCTACCCGCAGCCCACCACCCACCCAAGCCCGCCGGCAGGACTGTGCACGCCGCTGAGCAGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56224384..56224514 26863196 MeRIP-seq:(Medium) rs961353894 Functional Loss SNV dbSNP153 33..33 33 - - - 90905 RMVar_ID_90905 Human_SNP_ID_502352885 m1A Human chr12 + 56224467 56224467 56224467 GGCTTGGGTGGGTGGTGGGCTGCGGGTAGGGGAGGGGATGGACCGAGTCCCGGCTTGTCGGGATG GGCTTGGGTGGGTGGTGGGCTGCGGGTAGGGGCGGGGATGGACCGAGTCCCGGCTTGTCGGGATG A C NABP2 Ensembl:ENSG00000139579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56224419..56224566 26863196 MeRIP-seq:(Medium) rs1474887462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230018,Human_RBP_ID_873101,Human_RBP_ID_4246144,Human_RBP_ID_5235435,Human_RBP_ID_6200563,Human_RBP_ID_9323136,Human_RBP_ID_9416108,Human_RBP_ID_25024886 Human_Splice_Rec_1382449 90906 RMVar_ID_90906 Human_SNP_ID_502357047 m1A Human chr12 - 56238044 56238044 56238044 GATGCCTGCATCCCCAGGGTGCCGAGGGCAGCAGGAAAAAGTGGGGACCTCGGTGCATTTGCCCC GATGCCTGCATCCCCAGGGTGCCGAGGGCAGCGGGAAAAAGTGGGGACCTCGGTGCATTTGCCCC T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56237955..56238405 32194978 MeRIP-seq:(Medium) rs1348614882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1092797,Human_miRNA_ID_2512279,Human_miRNA_ID_3055100 RMVar_hsa_circ_106953,RMVar_hsa_circ_125101,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_101351,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157273,RMVar_hsa_circ_157274,RMVar_hsa_circ_157272 90907 RMVar_ID_90907 Human_SNP_ID_502357585 m1A Human chr12 - 56240352 56240352 56240352 GGTCCCAGCAAAGGAAACAGAGCGAGGGCGACATAGGAGACAGGGAAACAGACGTGTGAATCAGA GGTCCCAGCAAAGGAAACAGAGCGAGGGCGACGTAGGAGACAGGGAAACAGACGTGTGAATCAGA T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56240301..56240398 26863196 MeRIP-seq:(Medium) rs530887351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6200608,Human_RBP_ID_11986379 Human_miRNA_ID_541632,Human_miRNA_ID_966516,Human_miRNA_ID_2191683,Human_miRNA_ID_2444167 RMVar_hsa_circ_106953,RMVar_hsa_circ_125101,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_101351,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157273,RMVar_hsa_circ_157274,RMVar_hsa_circ_157272 90908 RMVar_ID_90908 Human_SNP_ID_502357771 m1A Human chr12 + 56241120 56241119 56241120 GCCCTTAAGAGAGGTCACATTGATTGTCATATAGGGGAGGACACGGTGTGGAGGGAGGTGGGCAA GCCCTTAAGAGAGGTCACATTGATTGTCATAT_GGGGAGGACACGGTGTGGAGGGAGGTGGGCAA TA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56241070..56241167 26863196 MeRIP-seq:(Medium) rs1416741172 Functional Loss DEL dbSNP153 33..33 33 - - - 90909 RMVar_ID_90909 Human_SNP_ID_502358105 m1A Human chr12 - 56242703 56242703 56242703 CATCACTGCCTCCCTGCTCGGCCGGTCCCTCCATCCCCGCAGCAGTGAGAAGCCTTAATTTCTGG CATCACTGCCTCCCTGCTCGGCCGGTCCCTCCGTCCCCGCAGCAGTGAGAAGCCTTAATTTCTGG T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56242652..56242885 26863196 MeRIP-seq:(Medium) rs1565606416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423861,Human_RBP_ID_17075112,Human_RBP_ID_17357648,Human_RBP_ID_18934546,Human_RBP_ID_19788358 RMVar_hsa_circ_106953,RMVar_hsa_circ_125101,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_101351,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157273,RMVar_hsa_circ_157274,RMVar_hsa_circ_157272 90910 RMVar_ID_90910 Human_SNP_ID_502362242 m1A Human chr12 - 56257697 56257697 56257697 GATGAGGCCGCAGTTCTTTCCATCCTGGAGTGAAAGCCTACTCTGCATTTGGGGATGGAGAGCAG GATGAGGCCGCAGTTCTTTCCATCCTGGAGTGGAAGCCTACTCTGCATTTGGGGATGGAGAGCAG T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56257647..56257786 32194978 MeRIP-seq:(Medium) rs1565613613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23566770 RMVar_hsa_circ_111834,RMVar_hsa_circ_157278,RMVar_hsa_circ_120013,RMVar_hsa_circ_110249,RMVar_hsa_circ_157292,RMVar_hsa_circ_157293,RMVar_hsa_circ_104582,RMVar_hsa_circ_157302,RMVar_hsa_circ_80461,RMVar_hsa_circ_157303,RMVar_hsa_circ_122570,RMVar_hsa_circ_119595,RMVar_hsa_circ_157314,RMVar_hsa_circ_157316 90911 RMVar_ID_90911 Human_SNP_ID_502362539 m1A Human chr12 + 56258511 56258510 56258511 AGCGCCCTCCGCCCCACCCTGGCGGCCCCAGCAGCCCCTGCACCCCCGAACTCGCGCGCCGGCTC AGCGCCCTCCGCCCCACCCTGGCGGCCCCAGC_GCCCCTGCACCCCCGAACTCGCGCGCCGGCTC CA C HSALNG0091520 RNACentral:URS0000EA4272 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56258461..56258647 26863196 MeRIP-seq:(Medium) rs1241241019 Functional Loss DEL dbSNP153 33..33 33 - - - 90912 RMVar_ID_90912 Human_SNP_ID_502364705 m1A Human chr12 - 56266947 56266947 56266947 GCCTTGCTCCCGTCCAGGCTGCCGGGTAGGCTAGAACTGAAGCCGGGACCGCTGCTCCCGCAGAT GCCTTGCTCCCGTCCAGGCTGCCGGGTAGGCTGGAACTGAAGCCGGGACCGCTGCTCCCGCAGAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56266918..56267094 26863196 MeRIP-seq:(Medium) rs941867584 Functional Loss SNV dbSNP153 33..33 33 - - - 90913 RMVar_ID_90913 Human_SNP_ID_502364717 m1A Human chr12 - 56266986 56266986 56266986 CTCTGAGCGCAGGGGCGACGGGAGGCGGCAGCACCTCTCGCCTTGCTCCCGTCCAGGCTGCCGGG CTCTGAGCGCAGGGGCGACGGGAGGCGGCAGCTCCTCTCGCCTTGCTCCCGTCCAGGCTGCCGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56266935..56267038 26863196 MeRIP-seq:(Medium) rs1477192088 Functional Loss SNV dbSNP153 33..33 33 - - - 90914 RMVar_ID_90914 Human_SNP_ID_502364721 m1A Human chr12 - 56266996 56266996 56266996 GGTTCGGGACCTCTGAGCGCAGGGGCGACGGGAGGCGGCAGCACCTCTCGCCTTGCTCCCGTCCA GGTTCGGGACCTCTGAGCGCAGGGGCGACGGGCGGCGGCAGCACCTCTCGCCTTGCTCCCGTCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56266946..56267043 26863196 MeRIP-seq:(Medium) rs377753035 Functional Loss SNV dbSNP153 33..33 33 - - - 90915 RMVar_ID_90915 Human_SNP_ID_502364852 m1A Human chr12 - 56267330 56267330 56267330 ATTGCTGCCAGTCCCCGCCGCGCCTGCATCCCAGTATAGCACCCCTCCACCGCGGAACCCCGGGG ATTGCTGCCAGTCCCCGCCGCGCCTGCATCCCGGTATAGCACCCCTCCACCGCGGAACCCCGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56267280..56267391 26863196 MeRIP-seq:(Medium) rs1205927730 Functional Loss SNV dbSNP153 33..33 33 - - - 90916 RMVar_ID_90916 Human_SNP_ID_502366221 m1A Human chr12 + 56272886 56272885 56272886 ACCATGCGTATGATGGGCAACTCATACCAGGCAGGGGAAGGGAGCTGATTAGGGAAGAAGGGACC ACCATGCGTATGATGGGCAACTCATACCAGGC_GGGGAAGGGAGCTGATTAGGGAAGAAGGGACC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56272836..56272910 26863196 MeRIP-seq:(Medium) rs761721390 Functional Loss DEL dbSNP153 33..33 33 - - - 90917 RMVar_ID_90917 Human_SNP_ID_502366222 m1A Human chr12 + 56272886 56272886 56272886 ACCATGCGTATGATGGGCAACTCATACCAGGCAGGGGAAGGGAGCTGATTAGGGAAGAAGGGACC ACCATGCGTATGATGGGCAACTCATACCAGGCGGGGGAAGGGAGCTGATTAGGGAAGAAGGGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56272836..56272910 26863196 MeRIP-seq:(Medium) rs1325472313 Functional Loss SNV dbSNP153 33..33 33 - - - 90918 RMVar_ID_90918 Human_SNP_ID_502366414 m1A Human chr12 + 56273746 56273746 56273746 AGGTGTTTCAGAGCAAACTCTCGCTGACAGGTATATCGCGGATCAGTCTTCCTTAGTACTGCATG AGGTGTTTCAGAGCAAACTCTCGCTGACAGGTGTATCGCGGATCAGTCTTCCTTAGTACTGCATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56273701..56273775 32194978 MeRIP-seq:(Medium) rs1171443173 Functional Loss SNV dbSNP153 33..33 33 - - - 90919 RMVar_ID_90919 Human_SNP_ID_502369672 m1A Human chr12 + 56285967 56285967 56285967 CCCACCACCGTCTTGCCATGTTGCTGCCTGAAAGTCTTAATTCTGGCCTGCTCCTTAGGTATCAG CCCACCACCGTCTTGCCATGTTGCTGCCTGAAGGTCTTAATTCTGGCCTGCTCCTTAGGTATCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56285897..56286007 26863196 MeRIP-seq:(Medium) rs1802236 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_514 GWAS_ID_11700,GWAS_ID_11701,GWAS_ID_11702,GWAS_ID_11703,GWAS_ID_11704,GWAS_ID_11705,GWAS_ID_11706,GWAS_ID_11707,GWAS_ID_11708,GWAS_ID_11709,GWAS_ID_11710,GWAS_ID_11711,GWAS_ID_11712,GWAS_ID_11713,GWAS_ID_11714,GWAS_ID_11715,GWAS_ID_11716,GWAS_ID_11717,GWAS_ID_11718,GWAS_ID_11719,GWAS_ID_11720,GWAS_ID_11721,GWAS_ID_11722,GWAS_ID_11723,GWAS_ID_11724,GWAS_ID_11725,GWAS_ID_11726,GWAS_ID_11727,GWAS_ID_11728,GWAS_ID_11729,GWAS_ID_11730,GWAS_ID_11731,GWAS_ID_11732,GWAS_ID_11733,GWAS_ID_11734,GWAS_ID_11735,GWAS_ID_11736,GWAS_ID_11737,GWAS_ID_11738,GWAS_ID_11739,GWAS_ID_11740,GWAS_ID_11741,GWAS_ID_11742,GWAS_ID_11743,GWAS_ID_11744,GWAS_ID_11745,GWAS_ID_11746,GWAS_ID_11747,GWAS_ID_11748,GWAS_ID_11749,GWAS_ID_11750,GWAS_ID_11751,GWAS_ID_11752,GWAS_ID_11753,GWAS_ID_11754,GWAS_ID_11755,GWAS_ID_11756,GWAS_ID_11757,GWAS_ID_11758,GWAS_ID_11759,GWAS_ID_11760,GWAS_ID_11761,GWAS_ID_11762,GWAS_ID_11763,GWAS_ID_11764,GWAS_ID_11765,GWAS_ID_11766,GWAS_ID_11767,GWAS_ID_11768,GWAS_ID_11769,GWAS_ID_11770,GWAS_ID_11771,GWAS_ID_11772,GWAS_ID_11773,GWAS_ID_11774,GWAS_ID_11775,GWAS_ID_11776,GWAS_ID_11777,GWAS_ID_11778,GWAS_ID_11779,GWAS_ID_11780,GWAS_ID_11781,GWAS_ID_11782,GWAS_ID_11783,GWAS_ID_11784,GWAS_ID_11785,GWAS_ID_11786,GWAS_ID_11787,GWAS_ID_11788,GWAS_ID_11789,GWAS_ID_11790,GWAS_ID_11791,GWAS_ID_11792,GWAS_ID_11793,GWAS_ID_11794,GWAS_ID_11795,GWAS_ID_11796,GWAS_ID_11797,GWAS_ID_11798,GWAS_ID_11799,GWAS_ID_11800,GWAS_ID_11801,GWAS_ID_11802,GWAS_ID_11803,GWAS_ID_11804,GWAS_ID_11805,GWAS_ID_11806,GWAS_ID_11807,GWAS_ID_11808,GWAS_ID_11809,GWAS_ID_11810,GWAS_ID_11811,GWAS_ID_11812 90920 RMVar_ID_90920 Human_SNP_ID_502373268 m1A Human chr12 - 56300250 56300250 56300250 GGTGCAGCGGCGGCGGCTCCTGTTCCTGCCGCAGCTCTCTCCCTTTCTTACCTCCCCACCAGATC GGTGCAGCGGCGGCGGCTCCTGTTCCTGCCGCCGCTCTCTCCCTTTCTTACCTCCCCACCAGATC T G CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr12:56300193..56300375;chr12:56300176..56300325 26863196,32194978 MeRIP-seq:(Medium) rs547076594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423955,Human_RBP_ID_4246759,Human_RBP_ID_5437855,Human_RBP_ID_5461974,Human_RBP_ID_5491794,Human_RBP_ID_9322569,Human_RBP_ID_18188834,Human_RBP_ID_18417604,Human_RBP_ID_18935422,Human_RBP_ID_19788583,Human_RBP_ID_27423608 Human_Splice_Rec_1382679,Human_Splice_Rec_1382697,Human_Splice_Rec_1382717,Human_Splice_Rec_1382743,Human_Splice_Rec_1382795,Human_Splice_Rec_1382809,Human_Splice_Rec_1382815,Human_Splice_Rec_1382823,Human_Splice_Rec_1382845,Human_Splice_Rec_1382875,Human_Splice_Rec_1382905,Human_Splice_Rec_1382921,Human_Splice_Rec_1382931,Human_Splice_Rec_1382941,Human_Splice_Rec_1382951,Human_Splice_Rec_1382961,Human_Splice_Rec_1382971,Human_Splice_Rec_1382977,Human_Splice_Rec_1382981,Human_Splice_Rec_1382983,Human_Splice_Rec_1382987,Human_Splice_Rec_1383003 Human_miRNA_ID_2136914,Human_miRNA_ID_2609558,Human_miRNA_ID_2665704 RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335 90921 RMVar_ID_90921 Human_SNP_ID_502376081 m1A Human chr12 - 56311321 56311321 56311321 TGAAGGAGTATGGGGAACAGATTGATCCTTCCACCCATCGCAAGAACTACGTACGTGTAGTGGGC TGAAGGAGTATGGGGAACAGATTGATCCTTCCGCCCATCGCAAGAACTACGTACGTGTAGTGGGC T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56311272..56311354 26863196 MeRIP-seq:(Medium) rs190375156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36860,Human_RBP_ID_1797739,Human_RBP_ID_17650757,Human_RBP_ID_17823088,Human_RBP_ID_18469188,Human_RBP_ID_18977353,Human_RBP_ID_23566856,Human_RBP_ID_26321578 Human_Splice_Rec_1382996,Human_Splice_Rec_1383040,Human_Splice_Rec_1383060,Human_Splice_Rec_1383066,Human_Splice_Rec_1383074 RMVar_hsa_circ_42536 90922 RMVar_ID_90922 Human_SNP_ID_502377105 m1A Human chr12 - 56315151 56315151 56315151 GGGCCCTGCTGGGAACCGCCTGGGCTCGGAGGAGCCAGGATCTCCACTGTGGAGGTAAAGGCACA GGGCCCTGCTGGGAACCGCCTGGGCTCGGAGGTGCCAGGATCTCCACTGTGGAGGTAAAGGCACA T A CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56315126..56315150 26863196 MeRIP-seq:(Medium) rs760669679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230050,Human_RBP_ID_754908,Human_RBP_ID_1474472,Human_RBP_ID_3941781,Human_RBP_ID_4232800,Human_RBP_ID_17830914,Human_RBP_ID_19056398,Human_RBP_ID_22436512 Human_Splice_Rec_1382992,Human_Splice_Rec_1382993,Human_Splice_Rec_1383008,Human_Splice_Rec_1383009,Human_Splice_Rec_1383016,Human_Splice_Rec_1383017,Human_Splice_Rec_1383036,Human_Splice_Rec_1383037,Human_Splice_Rec_1383056,Human_Splice_Rec_1383057,Human_Splice_Rec_1383070,Human_Splice_Rec_1383071,Human_Splice_Rec_1383075,Human_Splice_Rec_1383080,Human_Splice_Rec_1383081,Human_Splice_Rec_1383084,Human_Splice_Rec_1383085,Human_Splice_Rec_1383088,Human_Splice_Rec_1383089,Human_Splice_Rec_1383092 RMVar_hsa_circ_51646 90923 RMVar_ID_90923 Human_SNP_ID_502377321 m1A Human chr12 + 56315851 56315851 56315851 ACCTCTGCTCCCAGGGCCGCCGCCGTGGCCCAAGCGCTGGAAGACCGCTGGACTCTCACTTTGGC ACCTCTGCTCCCAGGGCCGCCGCCGTGGCCCAGGCGCTGGAAGACCGCTGGACTCTCACTTTGGC A G AC073896.2 Ensembl:ENSG00000257303 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56314803..56316126 26863196 MeRIP-seq:(Medium) rs1245183633 Functional Loss SNV dbSNP153 33..33 33 - - - 90924 RMVar_ID_90924 Human_SNP_ID_502377324 m1A Human chr12 - 56315856 56315856 56315856 CTGGGGCCAAAGTGAGAGTCCAGCGGTCTTCCAGCGCTTGGGCCACGGCGGCGGCCCTGGGAGCA CTGGGGCCAAAGTGAGAGTCCAGCGGTCTTCCGGCGCTTGGGCCACGGCGGCGGCCCTGGGAGCA T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56315104..56316077 26863196 MeRIP-seq:(Medium) rs1479670728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1127348,Human_RBP_ID_1358046,Human_RBP_ID_1474473,Human_RBP_ID_4246150,Human_RBP_ID_5139644,Human_RBP_ID_5491797,Human_RBP_ID_9322570,Human_RBP_ID_17650760,Human_RBP_ID_22436514,Human_RBP_ID_23566869,Human_RBP_ID_26320930,Human_RBP_ID_27806710 Human_Splice_Rec_1382991,Human_Splice_Rec_1383007,Human_Splice_Rec_1383015,Human_Splice_Rec_1383035,Human_Splice_Rec_1383063,Human_Splice_Rec_1383069,Human_Splice_Rec_1383083,Human_Splice_Rec_1383091 90925 RMVar_ID_90925 Human_SNP_ID_502377344 m1A Human chr12 - 56315912 56315912 56315912 TCTGGAGAATCCCGGACAGCCCTGCTCCCTGCAGCCAGGTGTAGTTTCGGGAGCCACTGGGGCCA TCTGGAGAATCCCGGACAGCCCTGCTCCCTGCTGCCAGGTGTAGTTTCGGGAGCCACTGGGGCCA T A CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:56315126..56316040 26863410 MeRIP-seq:(Medium) rs561953670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230051,Human_RBP_ID_4246151,Human_RBP_ID_6200989,Human_RBP_ID_22436514,Human_RBP_ID_26909258,Human_RBP_ID_27806710 Human_Splice_Rec_1382991,Human_Splice_Rec_1383007,Human_Splice_Rec_1383015,Human_Splice_Rec_1383035,Human_Splice_Rec_1383055,Human_Splice_Rec_1383063,Human_Splice_Rec_1383069,Human_Splice_Rec_1383083,Human_Splice_Rec_1383087,Human_Splice_Rec_1383091 90926 RMVar_ID_90926 Human_SNP_ID_502377345 m1A Human chr12 - 56315912 56315912 56315912 TCTGGAGAATCCCGGACAGCCCTGCTCCCTGCAGCCAGGTGTAGTTTCGGGAGCCACTGGGGCCA TCTGGAGAATCCCGGACAGCCCTGCTCCCTGCGGCCAGGTGTAGTTTCGGGAGCCACTGGGGCCA T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:56315126..56316040 26863410 MeRIP-seq:(Medium) rs561953670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230051,Human_RBP_ID_4246151,Human_RBP_ID_6200989,Human_RBP_ID_22436514,Human_RBP_ID_26909258,Human_RBP_ID_27806710 Human_Splice_Rec_1382991,Human_Splice_Rec_1383007,Human_Splice_Rec_1383015,Human_Splice_Rec_1383035,Human_Splice_Rec_1383055,Human_Splice_Rec_1383063,Human_Splice_Rec_1383069,Human_Splice_Rec_1383083,Human_Splice_Rec_1383087,Human_Splice_Rec_1383091 90927 RMVar_ID_90927 Human_SNP_ID_502377365 m1A Human chr12 + 56315964 56315964 56315964 GGGATTCTCCAGAGCGCTTCGCCGCCTGCCACACACGGGGTGTCCCGGCGACCGCCTGACCCAGC GGGATTCTCCAGAGCGCTTCGCCGCCTGCCACCCACGGGGTGTCCCGGCGACCGCCTGACCCAGC A C AC073896.2 Ensembl:ENSG00000257303 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56315114..56316075 26863196 MeRIP-seq:(Medium) rs1160987500 Functional Loss SNV dbSNP153 33..33 33 - - - 90928 RMVar_ID_90928 Human_SNP_ID_502378340 m1A Human chr12 + 56319924 56319924 56319924 AGACCCACCAGGTCCCCAATCTGTGGCATCTCATTCAGCATCAGTGGAATAAAGGTAGTATGTGT AGACCCACCAGGTCCCCAATCTGTGGCATCTCGTTCAGCATCAGTGGAATAAAGGTAGTATGTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56319862..56319967 26863196 MeRIP-seq:(Medium) rs1409891783 Functional Loss SNV dbSNP153 33..33 33 - - - 90929 RMVar_ID_90929 Human_SNP_ID_502379214 m1A Human chr12 - 56323112 56323112 56323112 GGCTTCCTTTCTCCATTCGCATGAAGATGACCAAAAACAAAGGGCTGGATGTTTGCAATTGGACT GGCTTCCTTTCTCCATTCGCATGAAGATGACCGAAAACAAAGGGCTGGATGTTTGCAATTGGACT T C PAN2 Ensembl:ENSG00000135473 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56322898..56323148 26863196 MeRIP-seq:(Medium) rs1473453492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34786,Human_RBP_ID_2345201,Human_RBP_ID_3943093,Human_RBP_ID_4232845,Human_RBP_ID_8380017,Human_RBP_ID_9365068,Human_RBP_ID_18262195,Human_RBP_ID_18975772,Human_RBP_ID_22906225,Human_RBP_ID_23566879,Human_RBP_ID_24984425,Human_RBP_ID_26322993,Human_RBP_ID_27805549 Human_Splice_Rec_1383124,Human_Splice_Rec_1383125,Human_Splice_Rec_1383174,Human_Splice_Rec_1383175,Human_Splice_Rec_1383222,Human_Splice_Rec_1383223,Human_Splice_Rec_1383272,Human_Splice_Rec_1383273,Human_Splice_Rec_1383298,Human_Splice_Rec_1383344,Human_Splice_Rec_1383345,Human_Splice_Rec_1383394,Human_Splice_Rec_1383395 Human_miRNA_ID_2001867,Human_miRNA_ID_2003251,Human_miRNA_ID_2898770,Human_miRNA_ID_2974054,Human_miRNA_ID_3007242 RMVar_hsa_circ_90927,RMVar_hsa_circ_95627,RMVar_hsa_circ_62764,RMVar_hsa_circ_157340,RMVar_hsa_circ_157341 90930 RMVar_ID_90930 Human_SNP_ID_502379333 m1A Human chr12 + 56323524 56323524 56323524 GTCCTTACCTCAGCCTGCATTCTCCAGAAATCAGCCTCTTTTGAGCTGTTCACCTCACAATTGAT GTCCTTACCTCAGCCTGCATTCTCCAGAAATCGGCCTCTTTTGAGCTGTTCACCTCACAATTGAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56323498..56323581 26863196 MeRIP-seq:(Medium) rs1279755757 Functional Loss SNV dbSNP153 33..33 33 - - - 90931 RMVar_ID_90931 Human_SNP_ID_502402832 m1A Human chr12 - 56417751 56417749 56417752 CAGAGTTGGGAGCTCCAGGAATCCAAAAGAAGAAACGATACCAGATTGAGGATGATGAGGATGAC CAGAGTTGGGAGCTCCAGGAATCCAAAAGAA___ACGATACCAGATTGAGGATGATGAGGATGAC TTTC T TIMELESS Ensembl:ENSG00000111602 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56417701..56417800 26863196 MeRIP-seq:(Medium) rs749149381 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1797795,Human_RBP_ID_4257507 Human_Splice_Rec_1384280,Human_Splice_Rec_1384336,Human_Splice_Rec_1384360 RMVar_hsa_circ_106918,RMVar_hsa_circ_157363 90932 RMVar_ID_90932 Human_SNP_ID_502402837 m1A Human chr12 + 56417777 56417777 56417777 ATCGTTTCTTCTTTTGGATTCCTGGAGCTCCCAACTCTGGTGCTGTGGGAACGATGGGGGTGAGA ATCGTTTCTTCTTTTGGATTCCTGGAGCTCCCTACTCTGGTGCTGTGGGAACGATGGGGGTGAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56417726..56417800 26863196 MeRIP-seq:(Medium) rs768881064 Functional Loss SNV dbSNP153 33..33 33 - - - 90933 RMVar_ID_90933 Human_SNP_ID_502410627 m1A Human chr12 + 56444746 56444741 56444746 GCTCATCTTAAGGGGGGAAAAATCCAACATAAAATAAAACTTTCCCCTTTGATCTCTTATTGGCT GCTCATCTTAAGGGGGGAAAAATCCAAC_____ATAAAACTTTCCCCTTTGATCTCTTATTGGCT CATAAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56444744..56444839 26863196 MeRIP-seq:(Medium) rs1194028608 Functional Loss DEL dbSNP153 29..33 33 - - - 90934 RMVar_ID_90934 Human_SNP_ID_502427714 m1A Human chr12 + 56511652 56511652 56511652 CTGAATGATGAATTAGAAATTATTGAAGGCATAAAGTTTGATCGAGGCTATATTTCTCCATACTT CTGAATGATGAATTAGAAATTATTGAAGGCATGAAGTTTGATCGAGGCTATATTTCTCCATACTT A G HSPD1P4 Ensembl:ENSG00000257576 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879157480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063939 Human_miRNA_ID_1892910 90935 RMVar_ID_90935 Human_SNP_ID_502429965 m1A Human chr12 - 56521837 56521837 56521837 CAGGAGGAGAGAGATGAAGGGGGGCTGCGGGCAGAGAATGAGCTCGGGCTGCTCCTTTACGTCAC CAGGAGGAGAGAGATGAAGGGGGGCTGCGGGCTGAGAATGAGCTCGGGCTGCTCCTTTACGTCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56521811..56521963 26863196 MeRIP-seq:(Medium) rs977147948 Functional Loss SNV dbSNP153 33..33 33 - - - 90936 RMVar_ID_90936 Human_SNP_ID_502446838 m1A Human chr12 + 56593395 56593395 56593395 CCAGGCTAGTGTCCAACTCCTGACCTCCAAACAGCTAATTTTTGTATTTTTAATAGAGACAGGTT CCAGGCTAGTGTCCAACTCCTGACCTCCAAACGGCTAATTTTTGTATTTTTAATAGAGACAGGTT A G RBMS2 Ensembl:ENSG00000076067 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10783794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11989156 GWAS_ID_11813,GWAS_ID_11814 90937 RMVar_ID_90937 Human_SNP_ID_502449040 m1A Human chr12 - 56600297 56600297 56600297 GGCTGCCCTGGAACAGAATGTAGAACGGCGGTACCTGCGGGAGCCCCTCTGGCCAACTCATGAGG GGCTGCCCTGGAACAGAATGTAGAACGGCGGTGCCTGCGGGAGCCCCTCTGGCCAACTCATGAGG T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56600246..56600686 32194978 MeRIP-seq:(Medium) rs200393909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229703,Human_RBP_ID_4257594,Human_RBP_ID_5461980,Human_RBP_ID_8783612,Human_RBP_ID_9255494,Human_RBP_ID_9278279,Human_RBP_ID_18975814 Human_Splice_Rec_1384899,Human_Splice_Rec_1384955,Human_Splice_Rec_1384979,Human_Splice_Rec_1385035 RMVar_hsa_circ_60919 90938 RMVar_ID_90938 Human_SNP_ID_502449382 m1A Human chr12 - 56601326 56601323 56601326 CTCTTCCACGCCCTTGGCTGGGTTGGCCCCTAAGAGGCGAGCAGGAGACCCTGGAGAAATGCCAC CTCTTCCACGCCCTTGGCTGGGTTGGCCCCTA___GGCGAGCAGGAGACCCTGGAGAAATGCCAC CTCT C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56601275..56601376 32194978 MeRIP-seq:(Medium) rs779043211 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_33384,Human_RBP_ID_228480,Human_RBP_ID_809458,Human_RBP_ID_878552,Human_RBP_ID_4257597,Human_RBP_ID_5111993,Human_RBP_ID_5140301,Human_RBP_ID_8787270,Human_RBP_ID_9255496,Human_RBP_ID_9279059,Human_RBP_ID_24557736 Human_Splice_Rec_1384892,Human_Splice_Rec_1384948,Human_Splice_Rec_1384972,Human_Splice_Rec_1385028,Human_Splice_Rec_1385052,Human_Splice_Rec_1385053 RMVar_hsa_circ_60919,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702 90939 RMVar_ID_90939 Human_SNP_ID_502449384 m1A Human chr12 - 56601326 56601326 56601326 CTCTTCCACGCCCTTGGCTGGGTTGGCCCCTAAGAGGCGAGCAGGAGACCCTGGAGAAATGCCAC CTCTTCCACGCCCTTGGCTGGGTTGGCCCCTAGGAGGCGAGCAGGAGACCCTGGAGAAATGCCAC T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56601275..56601376 32194978 MeRIP-seq:(Medium) rs201375127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33384,Human_RBP_ID_228480,Human_RBP_ID_809458,Human_RBP_ID_878552,Human_RBP_ID_4257597,Human_RBP_ID_5111993,Human_RBP_ID_5140301,Human_RBP_ID_8787270,Human_RBP_ID_9255496,Human_RBP_ID_9279059,Human_RBP_ID_24557736 Human_Splice_Rec_1384892,Human_Splice_Rec_1384948,Human_Splice_Rec_1384972,Human_Splice_Rec_1385028,Human_Splice_Rec_1385052,Human_Splice_Rec_1385053 RMVar_hsa_circ_60919,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702 90940 RMVar_ID_90940 Human_SNP_ID_502450890 m1A Human chr12 - 56606302 56606302 56606302 TGACTTCCCTTATGGTTTACAGGCCAGAAATAAGCGGAAACAAGAGACCAAGAGCTTAAAGCAGA TGACTTCCCTTATGGTTTACAGGCCAGAAATAGGCGGAAACAAGAGACCAAGAGCTTAAAGCAGA T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:56606221..56606341;chr12:56606226..56606325 26863196 MeRIP-seq:(Medium) rs1322669135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33402,Human_RBP_ID_809676,Human_RBP_ID_878558,Human_RBP_ID_2345332,Human_RBP_ID_8230053,Human_RBP_ID_9255498,Human_RBP_ID_9279067,Human_RBP_ID_24543083,Human_RBP_ID_26321625,Human_RBP_ID_27805572 Human_Splice_Rec_1384874,Human_Splice_Rec_1384875,Human_Splice_Rec_1384930,Human_Splice_Rec_1384931,Human_Splice_Rec_1385010,Human_Splice_Rec_1385011,Human_Splice_Rec_1385064,Human_Splice_Rec_1385065,Human_Splice_Rec_1385069,Human_Splice_Rec_1385078,Human_Splice_Rec_1385079 RMVar_hsa_circ_60919,RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_59138,RMVar_hsa_circ_58360 90941 RMVar_ID_90941 Human_SNP_ID_502450966 m1A Human chr12 + 56606605 56606602 56606605 AAGATGAAGTAAGTTGTAGGAAAAATTAACCTACTGTTTCATCTCTCTGATGTCCCTCACCTGCC AAGATGAAGTAAGTTGTAGGAAAAATTAAC___CTGTTTCATCTCTCTGATGTCCCTCACCTGCC CCTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56606603..56606774 26863196 MeRIP-seq:(Medium) rs756522007 Functional Loss DEL dbSNP153 31..33 33 - - - 90942 RMVar_ID_90942 Human_SNP_ID_502451840 m1A Human chr12 + 56609703 56609703 56609703 ATTCATCAACATTTTAGATACCTCATGGAGGGAGCAGAATCCCAAAGTAAGAAATACCACTGTAC ATTCATCAACATTTTAGATACCTCATGGAGGGGGCAGAATCCCAAAGTAAGAAATACCACTGTAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56609700..56609841 26863196 MeRIP-seq:(Medium) rs766992635 Functional Loss SNV dbSNP153 33..33 33 - - - 90943 RMVar_ID_90943 Human_SNP_ID_502451868 m1A Human chr12 - 56609796 56609796 56609796 TGAAACGGGGTCGAGGTCGGCCACCTAAGGTCAAAATCACTGAGCTATTGAACAAGACAGACAAC TGAAACGGGGTCGAGGTCGGCCACCTAAGGTCGAAATCACTGAGCTATTGAACAAGACAGACAAC T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:56609709..56609898;chr12:56609692..56609925 26863196 MeRIP-seq:(Medium) rs1348255382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_993515,Human_RBP_ID_1474582,Human_RBP_ID_4233463,Human_RBP_ID_8783670,Human_RBP_ID_17239710,Human_RBP_ID_27806747 Human_Splice_Rec_1384871,Human_Splice_Rec_1384927,Human_Splice_Rec_1385007,Human_Splice_Rec_1385061,Human_Splice_Rec_1385075 RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_4824,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 90944 RMVar_ID_90944 Human_SNP_ID_502457084 m1A Human chr12 + 56629819 56629819 56629819 CCCTCCCGGGGATTCCACCCCAAGTCCCCCACAGGAGTCATCTCCACCAGCCAGGCGGCTTCTCC CCCTCCCGGGGATTCCACCCCAAGTCCCCCACGGGAGTCATCTCCACCAGCCAGGCGGCTTCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56629813..56629991 26863196 MeRIP-seq:(Medium) rs1211397656 Functional Loss SNV dbSNP153 33..33 33 - - - 90945 RMVar_ID_90945 Human_SNP_ID_502459080 m1A Human chr12 - 56638232 56638221 56638232 TTCTGTGTAGGCTGCACAAGAGCCTTGATTGAAGATATATTCTTTCTGAACAGTATTTAAGGTTT TTCTGTGTAGGCTGCACAAGAGCCTTGATTGA___________TTCTGAACAGTATTTAAGGTTT AAGAATATATCT A ATP5F1B Ensembl:ENSG00000110955 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56638176..56638425 32194978 MeRIP-seq:(Medium) rs149735193 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_424208,Human_RBP_ID_993524,Human_RBP_ID_1167636,Human_RBP_ID_1474591,Human_RBP_ID_1797887,Human_RBP_ID_3409515,Human_RBP_ID_4257640,Human_RBP_ID_5111499,Human_RBP_ID_5139650,Human_RBP_ID_8380154,Human_RBP_ID_9018760,Human_RBP_ID_11989575,Human_RBP_ID_17241798,Human_RBP_ID_17357202,Human_RBP_ID_17472620,Human_RBP_ID_17650000,Human_RBP_ID_18176884,Human_RBP_ID_18262259,Human_RBP_ID_18629981,Human_RBP_ID_18935440,Human_RBP_ID_19703623,Human_RBP_ID_22493624,Human_RBP_ID_22912513,Human_RBP_ID_23207716,Human_RBP_ID_23567199,Human_RBP_ID_24407409,Human_RBP_ID_24467136,Human_RBP_ID_24985131,Human_RBP_ID_26418299,Human_RBP_ID_27631164 Human_miRNA_ID_1991705,Human_miRNA_ID_2140010 RMVar_hsa_circ_85227,RMVar_hsa_circ_118862,RMVar_hsa_circ_127607,RMVar_hsa_circ_126142,RMVar_hsa_circ_95555,RMVar_hsa_circ_109546,RMVar_hsa_circ_88878,RMVar_hsa_circ_157428,RMVar_hsa_circ_157430,RMVar_hsa_circ_157432,RMVar_hsa_circ_77423,RMVar_hsa_circ_157433,RMVar_hsa_circ_157431,RMVar_hsa_circ_157429,RMVar_hsa_circ_157426,RMVar_hsa_circ_157427 90946 RMVar_ID_90946 Human_SNP_ID_502459579 m1A Human chr12 - 56640115 56640115 56640115 ACTACGTTTGCCCATTTGGATGCTACCACTGTACTGTCGCGTGCCATTGCTGAGCTGGGCATCTA ACTACGTTTGCCCATTTGGATGCTACCACTGTTCTGTCGCGTGCCATTGCTGAGCTGGGCATCTA T A ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56640066..56640249 26863196 MeRIP-seq:(Medium) rs771224329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33820,Human_RBP_ID_424231,Human_RBP_ID_877206,Human_RBP_ID_1081968,Human_RBP_ID_1167643,Human_RBP_ID_1474609,Human_RBP_ID_1797896,Human_RBP_ID_3409525,Human_RBP_ID_4233592,Human_RBP_ID_6201515,Human_RBP_ID_8247750,Human_RBP_ID_8380171,Human_RBP_ID_8783711,Human_RBP_ID_9018765,Human_RBP_ID_11989634,Human_RBP_ID_17239736,Human_RBP_ID_19703627,Human_RBP_ID_22435990,Human_RBP_ID_22532498,Human_RBP_ID_22756816,Human_RBP_ID_22794793,Human_RBP_ID_23567209,Human_RBP_ID_26909472,Human_RBP_ID_27154917,Human_RBP_ID_27216710,Human_RBP_ID_27423707,Human_RBP_ID_27558150 Human_Splice_Rec_1385128,Human_Splice_Rec_1385146,Human_Splice_Rec_1385162,Human_Splice_Rec_1385174,Human_Splice_Rec_1385180,Human_Splice_Rec_1385190 Human_miRNA_ID_1935278,Human_miRNA_ID_2134242 RMVar_hsa_circ_85227,RMVar_hsa_circ_118862,RMVar_hsa_circ_127607,RMVar_hsa_circ_95555,RMVar_hsa_circ_109546,RMVar_hsa_circ_74767,RMVar_hsa_circ_157428,RMVar_hsa_circ_157430,RMVar_hsa_circ_157432,RMVar_hsa_circ_77423,RMVar_hsa_circ_157433,RMVar_hsa_circ_157431,RMVar_hsa_circ_157429,RMVar_hsa_circ_123639,RMVar_hsa_circ_315651,RMVar_hsa_circ_87740,RMVar_hsa_circ_112545,RMVar_hsa_circ_157434,RMVar_hsa_circ_157435,RMVar_hsa_circ_373395,RMVar_hsa_circ_302934,RMVar_hsa_circ_108564,RMVar_hsa_circ_157437,RMVar_hsa_circ_157438,RMVar_hsa_circ_157439,RMVar_hsa_circ_157436 90947 RMVar_ID_90947 Human_SNP_ID_502459585 m1A Human chr12 + 56640139 56640139 56640139 CGCGACAGTACAGTGGTAGCATCCAAATGGGCAAACGTAGTAGCAGGGGCAGGGTCAGTCAAGTC CGCGACAGTACAGTGGTAGCATCCAAATGGGCGAACGTAGTAGCAGGGGCAGGGTCAGTCAAGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56639939..56640224 26863196 MeRIP-seq:(Medium) rs1292257520 Functional Loss SNV dbSNP153 33..33 33 - - - 90948 RMVar_ID_90948 Human_SNP_ID_502459592 m1A Human chr12 + 56640151 56640151 56640151 GTGGTAGCATCCAAATGGGCAAACGTAGTAGCAGGGGCAGGGTCAGTCAAGTCATCAGCAGGCAC GTGGTAGCATCCAAATGGGCAAACGTAGTAGCTGGGGCAGGGTCAGTCAAGTCATCAGCAGGCAC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:56640057..56640261 26863196 MeRIP-seq:(Medium) rs1171635079 Functional Loss SNV dbSNP153 33..33 33 - - - 90949 RMVar_ID_90949 Human_SNP_ID_502460196 m1A Human chr12 - 56642414 56642414 56642414 TACATAGATGAAGATCTGATTTGTATAAAGGCAGGGTGCAGTGGTGCATCTCAGCTACTGAGGAG TACATAGATGAAGATCTGATTTGTATAAAGGCGGGGTGCAGTGGTGCATCTCAGCTACTGAGGAG T C ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56642412..56642868 26863196 MeRIP-seq:(Medium) rs957073878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5348483,Human_RBP_ID_19060322,Human_RBP_ID_22354180 RMVar_hsa_circ_85227,RMVar_hsa_circ_118862,RMVar_hsa_circ_127607,RMVar_hsa_circ_95555,RMVar_hsa_circ_74767,RMVar_hsa_circ_157430,RMVar_hsa_circ_157432,RMVar_hsa_circ_77423,RMVar_hsa_circ_157433,RMVar_hsa_circ_157431,RMVar_hsa_circ_157429,RMVar_hsa_circ_123639,RMVar_hsa_circ_87740,RMVar_hsa_circ_112545,RMVar_hsa_circ_157435,RMVar_hsa_circ_373395,RMVar_hsa_circ_108564,RMVar_hsa_circ_157437,RMVar_hsa_circ_157438,RMVar_hsa_circ_157439,RMVar_hsa_circ_157436 90950 RMVar_ID_90950 Human_SNP_ID_502460317 m1A Human chr12 + 56642793 56642793 56642793 GTCAGCCCAGTCAGAGCTACCCGGGCACGAGCACCAGGTGGTTCATTCATTTGACCATATACCAG GTCAGCCCAGTCAGAGCTACCCGGGCACGAGCCCCAGGTGGTTCATTCATTTGACCATATACCAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56642651..56642850 32194978 MeRIP-seq:(Medium) rs1044985091 Functional Loss SNV dbSNP153 33..33 33 - - - 90951 RMVar_ID_90951 Human_SNP_ID_502460512 m1A Human chr12 + 56643498 56643497 56643499 GCCTTCACGGGTCCTCTCACCAACACCAGCAAACACAGAGTAACCACCATGGGCTTTGGCGACAT GCCTTCACGGGTCCTCTCACCAACACCAGCAA__ACAGAGTAACCACCATGGGCTTTGGCGACAT AAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56643448..56643541 26863196 MeRIP-seq:(Medium) rs1391482711 Functional Loss DEL dbSNP153 33..34 33 - - - 90952 RMVar_ID_90952 Human_SNP_ID_502460625 m1A Human chr12 + 56643955 56643955 56643955 ATGAACTCTGGAGCCTCAGCATGAATGGGAGCAAATCTGTAAAGGTAGAAGAGAGGATAGTATCT ATGAACTCTGGAGCCTCAGCATGAATGGGAGCGAATCTGTAAAGGTAGAAGAGAGGATAGTATCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56643794..56644006 26863196 MeRIP-seq:(Medium) rs1461420427 Functional Loss SNV dbSNP153 33..33 33 - - - 90953 RMVar_ID_90953 Human_SNP_ID_502461211 m1A Human chr12 + 56645924 56645924 56645924 CGCTGAAGGGGTGAGTCTCCGCAAGGCCCCGGAGGCCGGAGCAGCGGCCACCCGACCCACAAACC CGCTGAAGGGGTGAGTCTCCGCAAGGCCCCGGCGGCCGGAGCAGCGGCCACCCGACCCACAAACC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56645876..56645975 32194978 MeRIP-seq:(Medium) rs1248989098 Functional Loss SNV dbSNP153 33..33 33 - - - 90954 RMVar_ID_90954 Human_SNP_ID_502466787 m1A Human chr12 - 56664777 56664777 56664777 CTCTTTCAGGATTCACAAGACAGTGATGATGAAAGTAAGTGTATATAAAAAGTATGTTTATACAG CTCTTTCAGGATTCACAAGACAGTGATGATGACAGTAAGTGTATATAAAAAGTATGTTTATACAG T G PTGES3 Ensembl:ENSG00000110958 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1366296814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1474709,Human_RBP_ID_2368495,Human_RBP_ID_9344573,Human_RBP_ID_11990221,Human_RBP_ID_17830942,Human_RBP_ID_18630087,Human_RBP_ID_19058462,Human_RBP_ID_22437843,Human_RBP_ID_22645051,Human_RBP_ID_22736709,Human_RBP_ID_23567311 Human_Splice_Rec_1385208,Human_Splice_Rec_1385209,Human_Splice_Rec_1385224,Human_Splice_Rec_1385225,Human_Splice_Rec_1385238,Human_Splice_Rec_1385239,Human_Splice_Rec_1385250,Human_Splice_Rec_1385251,Human_Splice_Rec_1385262,Human_Splice_Rec_1385263,Human_Splice_Rec_1385274,Human_Splice_Rec_1385275,Human_Splice_Rec_1385284,Human_Splice_Rec_1385285 RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_157451 90955 RMVar_ID_90955 Human_SNP_ID_502474872 m1A Human chr12 + 56686843 56686843 56686843 TTCTAGCCAATATACTCAGCCTCAGTATCATGACTTGAATCAAGCAAATCCTTATTACTTTTCCA TTCTAGCCAATATACTCAGCCTCAGTATCATGTCTTGAATCAAGCAAATCCTTATTACTTTTCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56686840..56686927 26863196 MeRIP-seq:(Medium) rs1337137949 Functional Loss SNV dbSNP153 33..33 33 - - - 90956 RMVar_ID_90956 Human_SNP_ID_502475453 m1A Human chr12 - 56688083 56688083 56688083 GGCCGCGACCGGAGAGAAAAAGCGGAGTCGCCACCGGAGAGAAGTCGACTCCCTAGCAGCAGCCG GGCCGCGACCGGAGAGAAAAAGCGGAGTCGCCGCCGGAGAGAAGTCGACTCCCTAGCAGCAGCCG T C PTGES3 Ensembl:ENSG00000110958 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:56687976..56688260 26863196 MeRIP-seq:(Medium) rs11550107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33845,Human_RBP_ID_424339,Human_RBP_ID_878662,Human_RBP_ID_1798013,Human_RBP_ID_4233744,Human_RBP_ID_5437871,Human_RBP_ID_5461990,Human_RBP_ID_11991347,Human_RBP_ID_22437852,Human_RBP_ID_26321632 Human_Splice_Rec_1385211,Human_Splice_Rec_1385227,Human_Splice_Rec_1385241,Human_Splice_Rec_1385253,Human_Splice_Rec_1385265,Human_Splice_Rec_1385277 Human_miRNA_ID_3117922 RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 90957 RMVar_ID_90957 Human_SNP_ID_502475456 m1A Human chr12 - 56688098 56688098 56688098 AGGGAAGCGAGAAGAGGCCGCGACCGGAGAGAAAAAGCGGAGTCGCCACCGGAGAGAAGTCGACT AGGGAAGCGAGAAGAGGCCGCGACCGGAGAGAGAAAGCGGAGTCGCCACCGGAGAGAAGTCGACT T C PTGES3 Ensembl:ENSG00000110958 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:56687976..56688275;chr12:56687807..56688250 32194978 MeRIP-seq:(Medium) rs1183016693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33845,Human_RBP_ID_228651,Human_RBP_ID_811338,Human_RBP_ID_878662,Human_RBP_ID_4246782,Human_RBP_ID_8380330,Human_RBP_ID_9322579,Human_RBP_ID_9691914,Human_RBP_ID_22437852,Human_RBP_ID_22912551,Human_RBP_ID_25025235,Human_RBP_ID_26909563,Human_RBP_ID_27216765 RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 90958 RMVar_ID_90958 Human_SNP_ID_502482818 m1A Human chr12 - 56712840 56712840 56712840 TTGGTCATGTCACAAGCAAATGTGTCGAGAGCAAAGGCAGTCCGAGCCCTGAAGAACAACAGTAA TTGGTCATGTCACAAGCAAATGTGTCGAGAGCCAAGGCAGTCCGAGCCCTGAAGAACAACAGTAA T G NACA Ensembl:ENSG00000196531 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56712776..56712900 32194978 MeRIP-seq:(Medium) rs1363485347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35988,Human_RBP_ID_424350,Human_RBP_ID_754499,Human_RBP_ID_810679,Human_RBP_ID_876437,Human_RBP_ID_1474768,Human_RBP_ID_1798017,Human_RBP_ID_2345594,Human_RBP_ID_4233764,Human_RBP_ID_6202042,Human_RBP_ID_9018825,Human_RBP_ID_11991371,Human_RBP_ID_17239768,Human_RBP_ID_17357210,Human_RBP_ID_17474797,Human_RBP_ID_18630139,Human_RBP_ID_19789867,Human_RBP_ID_22040354,Human_RBP_ID_23567370,Human_RBP_ID_26909571,Human_RBP_ID_27216771 Human_Splice_Rec_1385304,Human_Splice_Rec_1385305,Human_Splice_Rec_1385320,Human_Splice_Rec_1385321,Human_Splice_Rec_1385336,Human_Splice_Rec_1385337,Human_Splice_Rec_1385350,Human_Splice_Rec_1385351,Human_Splice_Rec_1385364,Human_Splice_Rec_1385365,Human_Splice_Rec_1385378,Human_Splice_Rec_1385379,Human_Splice_Rec_1385384,Human_Splice_Rec_1385396,Human_Splice_Rec_1385397,Human_Splice_Rec_1385410,Human_Splice_Rec_1385411,Human_Splice_Rec_1385420,Human_Splice_Rec_1385421,Human_Splice_Rec_1385424,Human_Splice_Rec_1385436 Human_miRNA_ID_828883,Human_miRNA_ID_1767494,Human_miRNA_ID_2353753 RMVar_hsa_circ_1462,RMVar_hsa_circ_32403,RMVar_hsa_circ_157460,RMVar_hsa_circ_87659,RMVar_hsa_circ_363318,RMVar_hsa_circ_374015,RMVar_hsa_circ_72885,RMVar_hsa_circ_14130,RMVar_hsa_circ_157461 90959 RMVar_ID_90959 Human_SNP_ID_502483063 m1A Human chr12 + 56713663 56713663 56713663 ATAGTGACTCTAGTAACTCCTGTAACCTGCCGAAGACCCAGTTTGGACATAGCCTAAAGAAGAGA ATAGTGACTCTAGTAACTCCTGTAACCTGCCGGAGACCCAGTTTGGACATAGCCTAAAGAAGAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56713526..56713700 32194978 MeRIP-seq:(Medium) rs1282758283 Functional Loss SNV dbSNP153 33..33 33 - - - 90960 RMVar_ID_90960 Human_SNP_ID_502483344 m1A Human chr12 + 56714671 56714671 56714671 TCTTCAAGCTCTGGTACTGATTCATCACTGTCAGATTCTGTTCCAGACCCTAAGATGAGAAACAA TCTTCAAGCTCTGGTACTGATTCATCACTGTCGGATTCTGTTCCAGACCCTAAGATGAGAAACAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56714601..56714700 32194978 MeRIP-seq:(Medium) rs1355328093 Functional Loss SNV dbSNP153 33..33 33 - - - 90961 RMVar_ID_90961 Human_SNP_ID_502483978 m1A Human chr12 - 56716588 56716588 56716588 CCACTTCCCCACCTGTGACTCCTTCCTCCCTCAAAGACTCCCCTACTTCCCCAGCTTCTGTCACA CCACTTCCCCACCTGTGACTCCTTCCTCCCTCCAAGACTCCCCTACTTCCCCAGCTTCTGTCACA T G NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:56716587..56716770 26863196 MeRIP-seq:(Medium) rs1464487870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126889,Human_RBP_ID_9691934,Human_RBP_ID_17075117,Human_RBP_ID_18934562,Human_RBP_ID_24985881 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_100016,RMVar_hsa_circ_374757,RMVar_hsa_circ_157468 90962 RMVar_ID_90962 Human_SNP_ID_502484000 m1A Human chr12 - 56716642 56716641 56716642 TGACTCCTCCATCCCCCGAAAAGGGCCCAGCAACTCCAGCCCCCAAAGGGACTCCCACTTCCCCA TGACTCCTCCATCCCCCGAAAAGGGCCCAGCA_CTCCAGCCCCCAAAGGGACTCCCACTTCCCCA GT G NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56716622..56716975 26863196 MeRIP-seq:(Medium) rs1342877813 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5126889,Human_RBP_ID_17075565,Human_RBP_ID_26777109 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_100016,RMVar_hsa_circ_374757,RMVar_hsa_circ_157468 90963 RMVar_ID_90963 Human_SNP_ID_502484758 m1A Human chr12 + 56718203 56718140 56718204 GGGGTAGCTAGACCTCCTTTTGGGGAGGGAGGAGTTGCAGCTGGGGGCATGGGGGCCCCTTTGGG __________________________________TTGCAGCTGGGGGCATGGGGGCCCCTTTGGG AGCTGGGGTTGTGGGTGCCCCTTTGTGGGGTGGGGTAGCTAGACCTCCTTTTGGGGAGGGAGGAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56718200..56718699 26863196 MeRIP-seq:(Medium) rs1565895651 Functional Loss DEL dbSNP153 1..34 33 - - - 90964 RMVar_ID_90964 Human_SNP_ID_502484903 m1A Human chr12 + 56718406 56718406 56718406 GAGTGGGGTAGCTGCTGGACTTCCTTTGGGGGAGGGAGGAGTTGCAGCTGGGGGTGTGGATGCCC GAGTGGGGTAGCTGCTGGACTTCCTTTGGGGGGGGGAGGAGTTGCAGCTGGGGGTGTGGATGCCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:56718399..56718530 26863196 MeRIP-seq:(Medium) rs1387056571 Functional Loss SNV dbSNP153 33..33 33 - - - 90965 RMVar_ID_90965 Human_SNP_ID_502485057 m1A Human chr12 - 56718709 56718708 56718709 TCCCAGCTTCCCCATCCCCCAAAGGGGCCCCCACACCCCCAGCTGCAACTCCTCCCTCCCCTAAA TCCCAGCTTCCCCATCCCCCAAAGGGGCCCCC_CACCCCCAGCTGCAACTCCTCCCTCCCCTAAA GT G NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56718707..56718810 26863196 MeRIP-seq:(Medium) rs751595415 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17074876 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_100016,RMVar_hsa_circ_374757,RMVar_hsa_circ_157468 90966 RMVar_ID_90966 Human_SNP_ID_502485883 m1A Human chr12 - 56720785 56720785 56720785 CCCTAGCCATCGCTTCCCCTCAAGTCAAAGATACCACCATTTCCTCAGTTCTGATTTCTCCACAA CCCTAGCCATCGCTTCCCCTCAAGTCAAAGATGCCACCATTTCCTCAGTTCTGATTTCTCCACAA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56720782..56720866 26863196 MeRIP-seq:(Medium) rs1481902838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17075339 Human_miRNA_ID_2247307,Human_miRNA_ID_2851618 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_100016,RMVar_hsa_circ_374757,RMVar_hsa_circ_157468 90967 RMVar_ID_90967 Human_SNP_ID_502486942 m1A Human chr12 - 56724469 56724469 56724469 AACCGTCCCTGCTACAGAGCAGGAGTTGCCGCAGCCCCAGGCTGAGACAGGTAGGTTTCCCTACC AACCGTCCCTGCTACAGAGCAGGAGTTGCCGCGGCCCCAGGCTGAGACAGGTAGGTTTCCCTACC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:56724451..56724550;chr12:56724451..56724525 32194978 MeRIP-seq:(Medium) rs919205998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229479,Human_RBP_ID_424371,Human_RBP_ID_754510,Human_RBP_ID_876443,Human_RBP_ID_1474786,Human_RBP_ID_4257760,Human_RBP_ID_6202127,Human_RBP_ID_8380386,Human_RBP_ID_9018836,Human_RBP_ID_9365108,Human_RBP_ID_17239781,Human_RBP_ID_17357232,Human_RBP_ID_17475049,Human_RBP_ID_22437202,Human_RBP_ID_23582795,Human_RBP_ID_26321635,Human_RBP_ID_26909601,Human_RBP_ID_27216784 Human_Splice_Rec_1385288,Human_Splice_Rec_1385289,Human_Splice_Rec_1385308,Human_Splice_Rec_1385309,Human_Splice_Rec_1385324,Human_Splice_Rec_1385325,Human_Splice_Rec_1385340,Human_Splice_Rec_1385341,Human_Splice_Rec_1385354,Human_Splice_Rec_1385355,Human_Splice_Rec_1385368,Human_Splice_Rec_1385369,Human_Splice_Rec_1385386,Human_Splice_Rec_1385387,Human_Splice_Rec_1385400,Human_Splice_Rec_1385401,Human_Splice_Rec_1385414,Human_Splice_Rec_1385415,Human_Splice_Rec_1385426,Human_Splice_Rec_1385427,Human_Splice_Rec_1385438,Human_Splice_Rec_1385439,Human_Splice_Rec_1385446,Human_Splice_Rec_1385447,Human_Splice_Rec_1385456,Human_Splice_Rec_1385457,Human_Splice_Rec_1385468,Human_Splice_Rec_1385469,Human_Splice_Rec_1385476,Human_Splice_Rec_1385477,Human_Splice_Rec_1385482,Human_Splice_Rec_1385483,Human_Splice_Rec_1385488,Human_Splice_Rec_1385489,Human_Splice_Rec_1385494,Human_Splice_Rec_1385504,Human_Splice_Rec_1385505 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_374757 90968 RMVar_ID_90968 Human_SNP_ID_502486951 m1A Human chr12 - 56724506 56724506 56724506 ATTCCCTTCCTTCAGAAATGCCCGGCGAAGCCACAGAAACCGTCCCTGCTACAGAGCAGGAGTTG ATTCCCTTCCTTCAGAAATGCCCGGCGAAGCCGCAGAAACCGTCCCTGCTACAGAGCAGGAGTTG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56724426..56724556 26863196 MeRIP-seq:(Medium) rs1361647025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424372,Human_RBP_ID_754511,Human_RBP_ID_810687,Human_RBP_ID_876443,Human_RBP_ID_1474786,Human_RBP_ID_4257762,Human_RBP_ID_8380386,Human_RBP_ID_9365110,Human_RBP_ID_17241824,Human_RBP_ID_17357234,Human_RBP_ID_17475049,Human_RBP_ID_22437202,Human_RBP_ID_22794874,Human_RBP_ID_26323040,Human_RBP_ID_26909603 Human_Splice_Rec_1385288,Human_Splice_Rec_1385289,Human_Splice_Rec_1385308,Human_Splice_Rec_1385309,Human_Splice_Rec_1385324,Human_Splice_Rec_1385325,Human_Splice_Rec_1385340,Human_Splice_Rec_1385341,Human_Splice_Rec_1385354,Human_Splice_Rec_1385355,Human_Splice_Rec_1385368,Human_Splice_Rec_1385369,Human_Splice_Rec_1385386,Human_Splice_Rec_1385387,Human_Splice_Rec_1385400,Human_Splice_Rec_1385401,Human_Splice_Rec_1385414,Human_Splice_Rec_1385415,Human_Splice_Rec_1385426,Human_Splice_Rec_1385427,Human_Splice_Rec_1385438,Human_Splice_Rec_1385439,Human_Splice_Rec_1385446,Human_Splice_Rec_1385447,Human_Splice_Rec_1385456,Human_Splice_Rec_1385457,Human_Splice_Rec_1385468,Human_Splice_Rec_1385469,Human_Splice_Rec_1385476,Human_Splice_Rec_1385477,Human_Splice_Rec_1385482,Human_Splice_Rec_1385483,Human_Splice_Rec_1385488,Human_Splice_Rec_1385489,Human_Splice_Rec_1385494,Human_Splice_Rec_1385504,Human_Splice_Rec_1385505 Human_miRNA_ID_1767495 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_374757 90969 RMVar_ID_90969 Human_SNP_ID_502487151 m1A Human chr12 - 56725090 56725090 56725090 ACAAAATGGGGTCTGCGGTTGGTGTCCTGGCAAAAGCAGGGTAGAAGGGCTGCGGGGCGGGCCCA ACAAAATGGGGTCTGCGGTTGGTGTCCTGGCAGAAGCAGGGTAGAAGGGCTGCGGGGCGGGCCCA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:56725070..56725216 26863196 MeRIP-seq:(Medium) rs1308711316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424377,Human_RBP_ID_810689,Human_RBP_ID_1065472,Human_RBP_ID_1474795,Human_RBP_ID_5235437,Human_RBP_ID_6202140,Human_RBP_ID_9018841 RMVar_hsa_circ_83107,RMVar_hsa_circ_157467 90970 RMVar_ID_90970 Human_SNP_ID_502487209 m1A Human chr12 - 56725265 56725265 56725265 TTCTGCCGCCATCTTGGTTCCGCGTTCCCTGCACAGTAAGTACTTTCTGTGCCGCTACTGTCTAT TTCTGCCGCCATCTTGGTTCCGCGTTCCCTGCGCAGTAAGTACTTTCTGTGCCGCTACTGTCTAT T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding 5'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56725251..56725325 32194978 MeRIP-seq:(Medium) rs1366586919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424383,Human_RBP_ID_754514,Human_RBP_ID_810691,Human_RBP_ID_876445,Human_RBP_ID_1474800,Human_RBP_ID_4246788,Human_RBP_ID_8380394,Human_RBP_ID_8783781,Human_RBP_ID_9365113,Human_RBP_ID_17239782,Human_RBP_ID_17357235,Human_RBP_ID_18630164,Human_RBP_ID_19058471,Human_RBP_ID_22176049,Human_RBP_ID_26423879,Human_RBP_ID_27216788,Human_RBP_ID_27423786 Human_Splice_Rec_1385287,Human_Splice_Rec_1385307,Human_Splice_Rec_1385323,Human_Splice_Rec_1385339,Human_Splice_Rec_1385385,Human_Splice_Rec_1385399,Human_Splice_Rec_1385413,Human_Splice_Rec_1385437,Human_Splice_Rec_1385455,Human_Splice_Rec_1385467,Human_Splice_Rec_1385475,Human_Splice_Rec_1385481,Human_Splice_Rec_1385493,Human_Splice_Rec_1385502,Human_Splice_Rec_1385503 RMVar_hsa_circ_83107,RMVar_hsa_circ_157467 90971 RMVar_ID_90971 Human_SNP_ID_502487210 m1A Human chr12 - 56725265 56725265 56725265 TTCTGCCGCCATCTTGGTTCCGCGTTCCCTGCACAGTAAGTACTTTCTGTGCCGCTACTGTCTAT TTCTGCCGCCATCTTGGTTCCGCGTTCCCTGCCCAGTAAGTACTTTCTGTGCCGCTACTGTCTAT T G NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding 5'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56725251..56725325 32194978 MeRIP-seq:(Medium) rs1366586919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424383,Human_RBP_ID_754514,Human_RBP_ID_810691,Human_RBP_ID_876445,Human_RBP_ID_1474800,Human_RBP_ID_4246788,Human_RBP_ID_8380394,Human_RBP_ID_8783781,Human_RBP_ID_9365113,Human_RBP_ID_17239782,Human_RBP_ID_17357235,Human_RBP_ID_18630164,Human_RBP_ID_19058471,Human_RBP_ID_22176049,Human_RBP_ID_26423879,Human_RBP_ID_27216788,Human_RBP_ID_27423786 Human_Splice_Rec_1385287,Human_Splice_Rec_1385307,Human_Splice_Rec_1385323,Human_Splice_Rec_1385339,Human_Splice_Rec_1385385,Human_Splice_Rec_1385399,Human_Splice_Rec_1385413,Human_Splice_Rec_1385437,Human_Splice_Rec_1385455,Human_Splice_Rec_1385467,Human_Splice_Rec_1385475,Human_Splice_Rec_1385481,Human_Splice_Rec_1385493,Human_Splice_Rec_1385502,Human_Splice_Rec_1385503 RMVar_hsa_circ_83107,RMVar_hsa_circ_157467 90972 RMVar_ID_90972 Human_SNP_ID_502488633 m1A Human chr12 - 56730574 56730574 56730574 ACTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCGGTCTCCACTAAAAATAC ACTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCGACATGGTGAAACCCGGTCTCCACTAAAAATAC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048663560 Functional Loss SNV dbSNP153 33..33 33 - - - 90973 RMVar_ID_90973 Human_SNP_ID_502488666 m1A Human chr12 - 56730696 56730696 56730696 TATTTTTAGTAGAGACGGGGTTTCACTATGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs968564765 Functional Loss SNV dbSNP153 33..33 33 - - - 90974 RMVar_ID_90974 Human_SNP_ID_502488827 m1A Human chr12 - 56731351 56731351 56731351 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCACA GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCACA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1206430213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 90975 RMVar_ID_90975 Human_SNP_ID_502488829 m1A Human chr12 - 56731355 56731355 56731355 ACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGAT ACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCTGAGAT T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1024674689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 90976 RMVar_ID_90976 Human_SNP_ID_502493961 m1A Human chr12 - 56752267 56752267 56752267 AATGGAGACGTTTGACCCCACCGAGCTGCCCGAGCTGCTTAAACTTTATTACCGGAGGCTCTTTC AATGGAGACGTTTGACCCCACCGAGCTGCCCGCGCTGCTTAAACTTTATTACCGGAGGCTCTTTC T G PRIM1 Ensembl:ENSG00000198056 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56752148..56752309 26863196 MeRIP-seq:(Medium) rs1565908544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246790,Human_RBP_ID_18434504,Human_RBP_ID_23567462 Human_Splice_Rec_1385507,Human_Splice_Rec_1385529,Human_Splice_Rec_1385549,Human_Splice_Rec_1385587,Human_Splice_Rec_1385597,Human_Splice_Rec_1385601 90977 RMVar_ID_90977 Human_SNP_ID_502558496 m1A Human chr12 - 57004961 57004961 57004961 GGCCATCCATCTTTTTCTCTTGCTATCCACAGATTAACTGTGCTGATAAGGAGGTAATTTCATAG GGCCATCCATCTTTTTCTCTTGCTATCCACAGTTTAACTGTGCTGATAAGGAGGTAATTTCATAG T A ZBTB39 Ensembl:ENSG00000166860 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57004927..57004996 26863196 MeRIP-seq:(Medium) rs760970133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1385698 90978 RMVar_ID_90978 Human_SNP_ID_502558864 m1A Human chr12 - 57006469 57006456 57006470 GCCGGCGGCGCCGCCTCCTCGTCGGGCCGGGCACGGCGGGCCGGGGCCTTTGTGTGAAGCGGCGG GCCGGCGGCGCCGCCTCCTCGTCGGGCCGGG______________GCCTTTGTGTGAAGCGGCGG CCCCGGCCCGCCGTG C ZBTB39 Ensembl:ENSG00000166860 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57006367..57006507 26863196 MeRIP-seq:(Medium) rs1297148992 Functional Loss DEL dbSNP153 32..45 33 - - - Human_Splice_Rec_1385697 90979 RMVar_ID_90979 Human_SNP_ID_502558869 m1A Human chr12 - 57006469 57006466 57006469 GCCGGCGGCGCCGCCTCCTCGTCGGGCCGGGCACGGCGGGCCGGGGCCTTTGTGTGAAGCGGCGG GCCGGCGGCGCCGCCTCCTCGTCGGGCCGGGC___GCGGGCCGGGGCCTTTGTGTGAAGCGGCGG CCGT C ZBTB39 Ensembl:ENSG00000166860 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57006367..57006507 26863196 MeRIP-seq:(Medium) rs1246893412 Functional Loss DEL dbSNP153 33..35 33 - - - Human_Splice_Rec_1385697 90980 RMVar_ID_90980 Human_SNP_ID_502576804 m1A Human chr12 + 57078694 57078694 57078694 CACTGTCCCACCGCCCCCGACTCCCGAGCCCCAGGGCCCGGGACCAACTGCCGGCGAGACCGCCA CACTGTCCCACCGCCCCCGACTCCCGAGCCCCGGGGCCCGGGACCAACTGCCGGCGAGACCGCCA A G NONHSAG011408.2 RNACentral:URS00008B4182 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:57078606..57078750 26863196 MeRIP-seq:(Medium) rs761421340 Functional Loss SNV dbSNP153 33..33 33 - - - 90981 RMVar_ID_90981 Human_SNP_ID_502576814 m1A Human chr12 - 57078710 57078710 57078710 GCGGGAGGAATGAAAGTGGCGGTCTCGCCGGCAGTTGGTCCCGGGCCCTGGGGCTCGGGAGTCGG GCGGGAGGAATGAAAGTGGCGGTCTCGCCGGCGGTTGGTCCCGGGCCCTGGGGCTCGGGAGTCGG T C NEMP1 Ensembl:ENSG00000166881 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57078613..57078709 26863196 MeRIP-seq:(Medium) rs759631797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4234171,Human_RBP_ID_17113235,Human_RBP_ID_18417287,Human_RBP_ID_23207725 Human_Splice_Rec_1386011,Human_Splice_Rec_1386025,Human_Splice_Rec_1386041 90982 RMVar_ID_90982 Human_SNP_ID_502579716 m1A Human chr12 + 57089172 57089172 57089172 AGAAGACGTGGAGGGAGGGACAGAGCCTGGACAGCGGTGGACACGGCATCGTGCGCGGGGAAGAG AGAAGACGTGGAGGGAGGGACAGAGCCTGGACGGCGGTGGACACGGCATCGTGCGCGGGGAAGAG A G NAB2 Ensembl:ENSG00000166886 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57089124..57089313 26863196 MeRIP-seq:(Medium) rs544277888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874752,Human_RBP_ID_5349748,Human_RBP_ID_9416113,Human_RBP_ID_18977449,Human_RBP_ID_22437203 90983 RMVar_ID_90983 Human_SNP_ID_502579717 m1A Human chr12 + 57089172 57089172 57089172 AGAAGACGTGGAGGGAGGGACAGAGCCTGGACAGCGGTGGACACGGCATCGTGCGCGGGGAAGAG AGAAGACGTGGAGGGAGGGACAGAGCCTGGACTGCGGTGGACACGGCATCGTGCGCGGGGAAGAG A T NAB2 Ensembl:ENSG00000166886 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57089124..57089313 26863196 MeRIP-seq:(Medium) rs544277888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874752,Human_RBP_ID_5349748,Human_RBP_ID_9416113,Human_RBP_ID_18977449,Human_RBP_ID_22437203 90984 RMVar_ID_90984 Human_SNP_ID_502579781 m1A Human chr12 - 57089287 57089287 57089287 CCCTCCGCCCGGCGGCTGCTCGGCTGTGGGGGAAGGCGCTCTGTGCATGGACGGCCGGAGATCAC CCCTCCGCCCGGCGGCTGCTCGGCTGTGGGGGGAGGCGCTCTGTGCATGGACGGCCGGAGATCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57089238..57091552 32194978 MeRIP-seq:(Medium) rs889494200 Functional Loss SNV dbSNP153 33..33 33 - - - 90985 RMVar_ID_90985 Human_SNP_ID_502580528 m1A Human chr12 - 57091618 57091618 57091618 AGCCTCCTCTTCTCCTCCTGCCCCAACGTCCGACTCTGGAGTGCTCCGGCCTGGCCAGATCCGGG AGCCTCCTCTTCTCCTCCTGCCCCAACGTCCGCCTCTGGAGTGCTCCGGCCTGGCCAGATCCGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57091567..57091755 26863196 MeRIP-seq:(Medium) rs1314988151 Functional Loss SNV dbSNP153 33..33 33 - - - 90986 RMVar_ID_90986 Human_SNP_ID_502580877 m1A Human chr12 + 57092540 57092540 57092540 AGAGTGGAGCTCTTCTCTTTGTCCCGCCAAGTAGCCCGAGAGAGCACCTACTTGTCCTCCTTGAA AGAGTGGAGCTCTTCTCTTTGTCCCGCCAAGTGGCCCGAGAGAGCACCTACTTGTCCTCCTTGAA A G NAB2 Ensembl:ENSG00000166886 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57092490..57093117 32194978 MeRIP-seq:(Medium) rs766937210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1386064,Human_Splice_Rec_1386065,Human_Splice_Rec_1386074,Human_Splice_Rec_1386075,Human_Splice_Rec_1386085 90987 RMVar_ID_90987 Human_SNP_ID_502581779 m1A Human chr12 - 57095130 57095130 57095130 GAAGGAGCAGGTCCAGTGTTCCCAGGCCCCCAATTCTGGGGGCAAATGTTGCCACTTTTAGCTGG GAAGGAGCAGGTCCAGTGTTCCCAGGCCCCCAGTTCTGGGGGCAAATGTTGCCACTTTTAGCTGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57095080..57095229 32194978 MeRIP-seq:(Medium) rs192206681 Functional Loss SNV dbSNP153 33..33 33 - - - 90988 RMVar_ID_90988 Human_SNP_ID_502581780 m1A Human chr12 - 57095130 57095130 57095130 GAAGGAGCAGGTCCAGTGTTCCCAGGCCCCCAATTCTGGGGGCAAATGTTGCCACTTTTAGCTGG GAAGGAGCAGGTCCAGTGTTCCCAGGCCCCCACTTCTGGGGGCAAATGTTGCCACTTTTAGCTGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57095080..57095229 32194978 MeRIP-seq:(Medium) rs192206681 Functional Loss SNV dbSNP153 33..33 33 - - - 90989 RMVar_ID_90989 Human_SNP_ID_502582337 m1A Human chr12 + 57096925 57096925 57096925 TGTCTTCCACCATGGTCACATCTGAGCAGAGCAGGGGGTCAGGGCTGGACACAGCATGCTCCTGA TGTCTTCCACCATGGTCACATCTGAGCAGAGCCGGGGGTCAGGGCTGGACACAGCATGCTCCTGA A C NONHSAG011408.2 RNACentral:URS00008B4182 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57096876..57097084 26863196 MeRIP-seq:(Medium) rs748381508 Functional Loss SNV dbSNP153 33..33 33 - - - 90990 RMVar_ID_90990 Human_SNP_ID_502582727 m1A Human chr12 - 57098472 57098472 57098472 GTAAGTGAAAAACCTCATGGGGATACCATCCCACTCTAAGGGGGTGGGCATTTGAATTGTTAGAA GTAAGTGAAAAACCTCATGGGGATACCATCCCTCTCTAAGGGGGTGGGCATTTGAATTGTTAGAA T A STAT6 Ensembl:ENSG00000166888 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57098469..57098572 26863196 MeRIP-seq:(Medium) rs780715662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1386166 90991 RMVar_ID_90991 Human_SNP_ID_502585725 m1A Human chr12 + 57107292 57107292 57107292 GAAGTATTTGTCTGAAAGTGGCCACCAGCTTCAGGGGGTCCCTCTGATATATGCTCTACAGAAAT GAAGTATTTGTCTGAAAGTGGCCACCAGCTTCCGGGGGTCCCTCTGATATATGCTCTACAGAAAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57106751..57108183 26863196 MeRIP-seq:(Medium) rs483352723 Functional Loss SNV dbSNP153 33..33 33 - - - 90992 RMVar_ID_90992 Human_SNP_ID_502585731 m1A Human chr12 - 57107304 57107304 57107304 TTTACCACCCTCATTTCTGTAGAGCATATATCAGAGGGACCCCCTGAAGCTGGTGGCCACTTTCA TTTACCACCCTCATTTCTGTAGAGCATATATCGGAGGGACCCCCTGAAGCTGGTGGCCACTTTCA T C STAT6 Ensembl:ENSG00000166888 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57106774..57107714 26863196 MeRIP-seq:(Medium) rs1483954081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1386094,Human_Splice_Rec_1386095,Human_Splice_Rec_1386136,Human_Splice_Rec_1386137,Human_Splice_Rec_1386178,Human_Splice_Rec_1386179,Human_Splice_Rec_1386220,Human_Splice_Rec_1386221,Human_Splice_Rec_1386272,Human_Splice_Rec_1386273,Human_Splice_Rec_1386318,Human_Splice_Rec_1386319,Human_Splice_Rec_1386360,Human_Splice_Rec_1386361,Human_Splice_Rec_1386400,Human_Splice_Rec_1386401,Human_Splice_Rec_1386442,Human_Splice_Rec_1386443,Human_Splice_Rec_1386486,Human_Splice_Rec_1386487,Human_Splice_Rec_1386550,Human_Splice_Rec_1386551,Human_Splice_Rec_1386568,Human_Splice_Rec_1386569,Human_Splice_Rec_1386576,Human_Splice_Rec_1386577,Human_Splice_Rec_1386584,Human_Splice_Rec_1386585,Human_Splice_Rec_1386594,Human_Splice_Rec_1386595,Human_Splice_Rec_1386600,Human_Splice_Rec_1386601,Human_Splice_Rec_1386608 Human_miRNA_ID_877504,Human_miRNA_ID_1346992,Human_miRNA_ID_1809268,Human_miRNA_ID_2955988 RMVar_hsa_circ_11671,RMVar_hsa_circ_113600,RMVar_hsa_circ_157500,RMVar_hsa_circ_85877,RMVar_hsa_circ_363154,RMVar_hsa_circ_112169,RMVar_hsa_circ_157503,RMVar_hsa_circ_157505,RMVar_hsa_circ_13394,RMVar_hsa_circ_90377,RMVar_hsa_circ_157506 90993 RMVar_ID_90993 Human_SNP_ID_502586747 m1A Human chr12 - 57111320 57111320 57111320 CTGCTTACACTGAAGAGGGAGGACGGGAGAGGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAT CTGCTTACACTGAAGAGGGAGGACGGGAGAGGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAT T G STAT6 Ensembl:ENSG00000166888 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57111035..57111393 26863196 MeRIP-seq:(Medium) rs1351170392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17242947,Human_RBP_ID_18417290,Human_RBP_ID_23113280,Human_RBP_ID_23567727 90994 RMVar_ID_90994 Human_SNP_ID_502590892 m1A Human chr12 + 57128784 57128784 57128784 AGGGGGCGCACCCCCGTCAGCAGGCCCTCCCCAAGGGGCTCGGAACTCTACCTCTTCACCCACGC AGGGGGCGCACCCCCGTCAGCAGGCCCTCCCCGAGGGGCTCGGAACTCTACCTCTTCACCCACGC A G LRP1 Ensembl:ENSG00000123384 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57128738..57128883 26863196 MeRIP-seq:(Medium) rs1315624224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810975,Human_RBP_ID_877372,Human_RBP_ID_4246160,Human_RBP_ID_5521583,Human_RBP_ID_22436522 Human_miRNA_ID_2367441,Human_miRNA_ID_2937491,Human_miRNA_ID_3015236 RMVar_hsa_circ_80115,RMVar_hsa_circ_157507 90995 RMVar_ID_90995 Human_SNP_ID_502590899 m1A Human chr12 - 57128820 57128820 57128820 TGTTCTTATTCTTTCCTTCGGCAAAGCGCACCAGGGGCGTGGGTGAAGAGGTAGAGTTCCGAGCC TGTTCTTATTCTTTCCTTCGGCAAAGCGCACCGGGGGCGTGGGTGAAGAGGTAGAGTTCCGAGCC T C STAT6 Ensembl:ENSG00000166888 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57128769..57128926 26863196 MeRIP-seq:(Medium) rs1171164163 Functional Loss SNV dbSNP153 33..33 33 - - - 90996 RMVar_ID_90996 Human_SNP_ID_502599526 m1A Human chr12 - 57163035 57163035 57163035 GACCCTGGATCCTCCCCTCCCCACTCTTCGGCATCCTCCTGATGGGGTCTGCTTCCCACTCCCAC GACCCTGGATCCTCCCCTCCCCACTCTTCGGCGTCCTCCTGATGGGGTCTGCTTCCCACTCCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57163010..57163083 26863196 MeRIP-seq:(Medium) rs1299302438 Functional Loss SNV dbSNP153 33..33 33 - - - 90997 RMVar_ID_90997 Human_SNP_ID_502611630 m1A Human chr12 - 57205202 57205202 57205202 CCTCGTCAGAGCCGTCCCCGCAGTCATCGAACATGTTGCAGCGCAGGGAGGAGGAGAGGCAGCGC CCTCGTCAGAGCCGTCCCCGCAGTCATCGAACCTGTTGCAGCGCAGGGAGGAGGAGAGGCAGCGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57205151..57205225 32194978 MeRIP-seq:(Medium) rs1348124085 Functional Loss SNV dbSNP153 33..33 33 - - - 90998 RMVar_ID_90998 Human_SNP_ID_502615146 m1A Human chr12 - 57216859 57216833 57216860 GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGCGCGGCC GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGG___________________________CGCGGCC GCCGCCGCTCCCGCCGCTCCCGCCGCTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57216808..57217060 26863196 MeRIP-seq:(Medium) rs549105121 Functional Loss DEL dbSNP153 32..58 33 - - - 90999 RMVar_ID_90999 Human_SNP_ID_502615147 m1A Human chr12 - 57216859 57216833 57216860 GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGCGCGGCC GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGG__________________GAGCGGCGGCGCGGCC GCCGCCGCTCCCGCCGCTCCCGCCGCTC GCCGCCGCTC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57216808..57217060 26863196 MeRIP-seq:(Medium) rs549105121 Functional Loss DEL dbSNP153 32..49 33 - - - 91000 RMVar_ID_91000 Human_SNP_ID_502615148 m1A Human chr12 - 57216859 57216833 57216860 GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGCGGCGCGGCC GCGGGCGGCGGGGCGGCTGCGGGAGCGGCGG_________GAGCGGCGGGAGCGGCGGCGCGGCC GCCGCCGCTCCCGCCGCTCCCGCCGCTC GCCGCCGCTCCCGCCGCTC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57216808..57217060 26863196 MeRIP-seq:(Medium) rs549105121 Functional Loss DEL dbSNP153 32..40 33 - - - 91001 RMVar_ID_91001 Human_SNP_ID_502615192 m1A Human chr12 - 57216915 57216915 57216915 CAGGCTGGGCGGGTCTCGGGCAGGCGGGAGCCAGGCCTAGGGACGCGGGGCTCCGGGCGGGCGGC CAGGCTGGGCGGGTCTCGGGCAGGCGGGAGCCCGGCCTAGGGACGCGGGGCTCCGGGCGGGCGGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:57216805..57216975 26863410 MeRIP-seq:(Medium) rs1322968401 Functional Loss SNV dbSNP153 33..33 33 - - - 91002 RMVar_ID_91002 Human_SNP_ID_502615198 m1A Human chr12 - 57216926 57216926 57216926 GCTGAGCGGGGCAGGCTGGGCGGGTCTCGGGCAGGCGGGAGCCAGGCCTAGGGACGCGGGGCTCC GCTGAGCGGGGCAGGCTGGGCGGGTCTCGGGCGGGCGGGAGCCAGGCCTAGGGACGCGGGGCTCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57216844..57216939 26863410 MeRIP-seq:(Medium) rs778767597 Functional Loss SNV dbSNP153 33..33 33 - - - 91003 RMVar_ID_91003 Human_SNP_ID_502617394 m1A Human chr12 + 57225060 57225042 57225060 CCGACCAACCACACGGGGGCGCTGGCCCGGGCAGGGGCAGCCGGGGCGTTGCCCGCGCAGCGCAC CCGACCAACCACACG__________________GGGGCAGCCGGGGCGTTGCCCGCGCAGCGCAC GGGGGCGCTGGCCCGGGCA G NXPH4 Ensembl:ENSG00000182379 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:57224943..57225101 26863196 MeRIP-seq:(Medium) rs1565764250 Functional Loss DEL dbSNP153 16..33 33 - - - 91004 RMVar_ID_91004 Human_SNP_ID_502617682 m1A Human chr12 + 57225683 57225682 57225684 CTGTATCTTCGTCTCTTTCCTCAGCTTTGACTACAAACTGGTGCAGAAGGTGTGCCCAGACTATA CTGTATCTTCGTCTCTTTCCTCAGCTTTGACT__AAACTGGTGCAGAAGGTGTGCCCAGACTATA TAC T NXPH4 Ensembl:ENSG00000182379 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57225598..57225749 32194978 MeRIP-seq:(Medium) rs1422140508 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_424561,Human_RBP_ID_4234299,Human_RBP_ID_23567791,Human_RBP_ID_27423884 91005 RMVar_ID_91005 Human_SNP_ID_502617690 m1A Human chr12 - 57225712 57225712 57225712 TCCGAAGTAGGGGTGCTCACTCTGGAAGTTATAGTCTGGGCACACCTTCTGCACCAGTTTGTAGT TCCGAAGTAGGGGTGCTCACTCTGGAAGTTATGGTCTGGGCACACCTTCTGCACCAGTTTGTAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57225661..57225821 26863196 MeRIP-seq:(Medium) rs1565764766 Functional Loss SNV dbSNP153 33..33 33 - - - 91006 RMVar_ID_91006 Human_SNP_ID_502617808 m1A Human chr12 + 57226098 57226098 57226098 TAGGCTGCGCACTCCCTTTCCCCGCAGCTTTAATAACTCCTGGCCTGGCACCCTCACCCCACCCT TAGGCTGCGCACTCCCTTTCCCCGCAGCTTTAGTAACTCCTGGCCTGGCACCCTCACCCCACCCT A G NXPH4 Ensembl:ENSG00000182379 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57226047..57226242 26863196 MeRIP-seq:(Medium) rs1015023746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424572,Human_RBP_ID_18206385,Human_RBP_ID_27423885 91007 RMVar_ID_91007 Human_SNP_ID_502618694 m1A Human chr12 - 57229775 57229775 57229775 GCCGCCCAAAACAAAGAGAAGTACAGCATCGCAACTCGGAAGTCGCAGGAGGTCCAGCCACCAAC GCCGCCCAAAACAAAGAGAAGTACAGCATCGCCACTCGGAAGTCGCAGGAGGTCCAGCCACCAAC T G AC137834.2 Ensembl:ENSG00000276727 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57229726..57229871 26863196 MeRIP-seq:(Medium) rs370449392 Functional Loss SNV dbSNP153 33..33 33 - - - 91008 RMVar_ID_91008 Human_SNP_ID_502619436 m1A Human chr12 - 57232276 57232276 57232276 ACCCTAGAGCACTCACGTTGAGCTTATAGGGCATAGACTCGAAGAAGATGGACGTGGCTGATATC ACCCTAGAGCACTCACGTTGAGCTTATAGGGCTTAGACTCGAAGAAGATGGACGTGGCTGATATC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57232226..57232275 26863196 MeRIP-seq:(Medium) rs759718961 Functional Loss SNV dbSNP153 33..33 33 - - - 91009 RMVar_ID_91009 Human_SNP_ID_502619437 m1A Human chr12 - 57232276 57232276 57232276 ACCCTAGAGCACTCACGTTGAGCTTATAGGGCATAGACTCGAAGAAGATGGACGTGGCTGATATC ACCCTAGAGCACTCACGTTGAGCTTATAGGGCGTAGACTCGAAGAAGATGGACGTGGCTGATATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57232226..57232275 26863196 MeRIP-seq:(Medium) rs759718961 Functional Loss SNV dbSNP153 33..33 33 - - - 91010 RMVar_ID_91010 Human_SNP_ID_502619494 m1A Human chr12 - 57232461 57232461 57232461 GTCAGTGCCAGCTGGTTGTAGTCAATGAGGCCAGTTTTGGGCTGGACAGACACACAAACAGCTAA GTCAGTGCCAGCTGGTTGTAGTCAATGAGGCCGGTTTTGGGCTGGACAGACACACAAACAGCTAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57232436..57232550 26863196 MeRIP-seq:(Medium) rs1025511284 Functional Loss SNV dbSNP153 33..33 33 - - - 91011 RMVar_ID_91011 Human_SNP_ID_502619678 m1A Human chr12 + 57233058 57233058 57233058 GGATTGAGGGGCTGATTCCCTCTACCACTGGAATCCAGTGTACCAAGCCCACGTGAGCTGTGCCC GGATTGAGGGGCTGATTCCCTCTACCACTGGACTCCAGTGTACCAAGCCCACGTGAGCTGTGCCC A C SHMT2 Ensembl:ENSG00000182199 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57233053..57233154 32194978 MeRIP-seq:(Medium) rs747736934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1474933 RMVar_hsa_circ_56302,RMVar_hsa_circ_92640,RMVar_hsa_circ_157619,RMVar_hsa_circ_353669 91012 RMVar_ID_91012 Human_SNP_ID_502619870 m1A Human chr12 + 57233661 57233661 57233661 GCCCTGCTAGAGCGAGGCTACTCACTGGTATCAGGTAAGCCAGCAGGTGATGGGTGAGGGCCTCT GCCCTGCTAGAGCGAGGCTACTCACTGGTATCCGGTAAGCCAGCAGGTGATGGGTGAGGGCCTCT A C SHMT2 Ensembl:ENSG00000182199 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57233551..57233675 32194978 MeRIP-seq:(Medium) rs1214479792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229361,Human_RBP_ID_18977531,Human_RBP_ID_19056512,Human_RBP_ID_22437248,Human_RBP_ID_22756010 Human_Splice_Rec_1386924,Human_Splice_Rec_1386925,Human_Splice_Rec_1386955,Human_Splice_Rec_1386974,Human_Splice_Rec_1386975,Human_Splice_Rec_1386996,Human_Splice_Rec_1386997,Human_Splice_Rec_1387018,Human_Splice_Rec_1387019,Human_Splice_Rec_1387066,Human_Splice_Rec_1387067,Human_Splice_Rec_1387088,Human_Splice_Rec_1387089,Human_Splice_Rec_1387108,Human_Splice_Rec_1387109,Human_Splice_Rec_1387168,Human_Splice_Rec_1387169,Human_Splice_Rec_1387206,Human_Splice_Rec_1387207,Human_Splice_Rec_1387226,Human_Splice_Rec_1387227,Human_Splice_Rec_1387246,Human_Splice_Rec_1387247,Human_Splice_Rec_1387268,Human_Splice_Rec_1387269,Human_Splice_Rec_1387306,Human_Splice_Rec_1387307,Human_Splice_Rec_1387311 RMVar_hsa_circ_32481,RMVar_hsa_circ_56302,RMVar_hsa_circ_92640,RMVar_hsa_circ_157619,RMVar_hsa_circ_353669,RMVar_hsa_circ_91574,RMVar_hsa_circ_157623 91013 RMVar_ID_91013 Human_SNP_ID_502620043 m1A Human chr12 - 57234084 57234084 57234084 ACTCACCAGTCTTGCTCTTCACCTCTAAGCCAATGTTGACCCCTTCATCTATAAAGTCCACAACT ACTCACCAGTCTTGCTCTTCACCTCTAAGCCAGTGTTGACCCCTTCATCTATAAAGTCCACAACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57234007..57234117 26863196 MeRIP-seq:(Medium) rs1294243777 Functional Loss SNV dbSNP153 33..33 33 - - - 91014 RMVar_ID_91014 Human_SNP_ID_502620490 m1A Human chr12 - 57235454 57235437 57235455 CCAAGGCATCACTCCGGCCACCCTGTCCCGCTACTGCTTACACAGGCCGGGTTCCCACGCAGAGG CCAAGGCATCACTCCGGCCACCCTGTCCCGC__________________GGTTCCCACGCAGAGG CCGGCCTGTGTAAGCAGTA C NDUFA4L2 Ensembl:ENSG00000185633 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57235406..57235524 26863196 MeRIP-seq:(Medium) rs374700944 Functional Loss DEL dbSNP153 32..49 33 - - - 91015 RMVar_ID_91015 Human_SNP_ID_502627085 m1A Human chr12 - 57258023 57258023 57258023 TCTGCACAGGACTCAGTCCCCTGCCTGTCCTCACACAGTTCCCCCGGCCTGGGGGTCCAGCACAG TCTGCACAGGACTCAGTCCCCTGCCTGTCCTCTCACAGTTCCCCCGGCCTGGGGGTCCAGCACAG T A AC137834.1,R3HDM2 Ensembl:ENSG00000258830,Ensembl:ENSG00000179912 Protein coding,Protein coding 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57256494..57258973 32194978 MeRIP-seq:(Medium) rs772025551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8380569,Human_RBP_ID_17243275 Human_Splice_Rec_1387455,Human_Splice_Rec_1387483,Human_Splice_Rec_1387529,Human_Splice_Rec_1387571,Human_Splice_Rec_1387615,Human_Splice_Rec_1387661,Human_Splice_Rec_1387707,Human_Splice_Rec_1387735,Human_Splice_Rec_1387781,Human_Splice_Rec_1387793,Human_Splice_Rec_1387805 Human_miRNA_ID_1962294,Human_miRNA_ID_2945786 RMVar_hsa_circ_6962,RMVar_hsa_circ_157630,RMVar_hsa_circ_347721,RMVar_hsa_circ_367619 91016 RMVar_ID_91016 Human_SNP_ID_502627086 m1A Human chr12 - 57258023 57258023 57258023 TCTGCACAGGACTCAGTCCCCTGCCTGTCCTCACACAGTTCCCCCGGCCTGGGGGTCCAGCACAG TCTGCACAGGACTCAGTCCCCTGCCTGTCCTCGCACAGTTCCCCCGGCCTGGGGGTCCAGCACAG T C AC137834.1,R3HDM2 Ensembl:ENSG00000258830,Ensembl:ENSG00000179912 Protein coding,Protein coding 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57256494..57258973 32194978 MeRIP-seq:(Medium) rs772025551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8380569,Human_RBP_ID_17243275 Human_Splice_Rec_1387455,Human_Splice_Rec_1387483,Human_Splice_Rec_1387529,Human_Splice_Rec_1387571,Human_Splice_Rec_1387615,Human_Splice_Rec_1387661,Human_Splice_Rec_1387707,Human_Splice_Rec_1387735,Human_Splice_Rec_1387781,Human_Splice_Rec_1387793,Human_Splice_Rec_1387805 Human_miRNA_ID_1962294,Human_miRNA_ID_2945786 RMVar_hsa_circ_6962,RMVar_hsa_circ_157630,RMVar_hsa_circ_347721,RMVar_hsa_circ_367619 91017 RMVar_ID_91017 Human_SNP_ID_502629798 m1A Human chr12 + 57269872 57269872 57269872 AGGGGCTGACCCGTGGAAGCCATGATGAAGCTAGTCTGCTGAGGGTGCTGGGAGATAAGTGGGGT AGGGGCTGACCCGTGGAAGCCATGATGAAGCTGGTCTGCTGAGGGTGCTGGGAGATAAGTGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57269821..57269940 26863196 MeRIP-seq:(Medium) rs777453984 Functional Loss SNV dbSNP153 33..33 33 - - - 91018 RMVar_ID_91018 Human_SNP_ID_502633031 m1A Human chr12 - 57284031 57284031 57284031 TCTGCAGGGGGAACCGTGAAGGACTGAGCCGCACCTCAAGCAGCCGCCAGAGCAGCACAGACAGC TCTGCAGGGGGAACCGTGAAGGACTGAGCCGCCCCTCAAGCAGCCGCCAGAGCAGCACAGACAGC T G AC137834.1,R3HDM2 Ensembl:ENSG00000258830,Ensembl:ENSG00000179912 Protein coding,Protein coding 3'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57283935..57284035 32194978 MeRIP-seq:(Medium) rs1170365661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811521,Human_RBP_ID_3941870,Human_RBP_ID_22645922 Human_Splice_Rec_1387438,Human_Splice_Rec_1387466,Human_Splice_Rec_1387512,Human_Splice_Rec_1387554,Human_Splice_Rec_1387596,Human_Splice_Rec_1387644,Human_Splice_Rec_1387690,Human_Splice_Rec_1387718,Human_Splice_Rec_1387762,Human_Splice_Rec_1387818,Human_Splice_Rec_1387824 Human_miRNA_ID_2907840,Human_miRNA_ID_3026678 RMVar_hsa_circ_43240,RMVar_hsa_circ_157630,RMVar_hsa_circ_367619,RMVar_hsa_circ_356080,RMVar_hsa_circ_329886,RMVar_hsa_circ_157631,RMVar_hsa_circ_157633,RMVar_hsa_circ_69120,RMVar_hsa_circ_157639,RMVar_hsa_circ_157635,RMVar_hsa_circ_277044,RMVar_hsa_circ_300128,RMVar_hsa_circ_356256,RMVar_hsa_circ_366067,RMVar_hsa_circ_371654,RMVar_hsa_circ_344725,RMVar_hsa_circ_297905,RMVar_hsa_circ_157637,RMVar_hsa_circ_73817,RMVar_hsa_circ_157636,RMVar_hsa_circ_322159,RMVar_hsa_circ_354313,RMVar_hsa_circ_157634,RMVar_hsa_circ_367485,RMVar_hsa_circ_346166,RMVar_hsa_circ_301461,RMVar_hsa_circ_301611,RMVar_hsa_circ_157640,RMVar_hsa_circ_157638 91019 RMVar_ID_91019 Human_SNP_ID_502674647 m1A Human chr12 - 57457229 57457229 57457229 GCCTGCTTACCCTGCTTCAAGCCTGCTGGACCATCTATCTGCTTCCTCCTCCCCTCACTTGAGGA GCCTGCTTACCCTGCTTCAAGCCTGCTGGACCGTCTATCTGCTTCCTCCTCCCCTCACTTGAGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57457191..57457285 26863196 MeRIP-seq:(Medium) rs1421183389 Functional Loss SNV dbSNP153 33..33 33 - - - 91020 RMVar_ID_91020 Human_SNP_ID_502674649 m1A Human chr12 + 57457249 57457249 57457249 GAAGCAGATAGATGGTCCAGCAGGCTTGAAGCAGGGTAAGCAGGCTGGCCCAGGGTAAGGGCTGT GAAGCAGATAGATGGTCCAGCAGGCTTGAAGCCGGGTAAGCAGGCTGGCCCAGGGTAAGGGCTGT A C INHBE Ensembl:ENSG00000139269 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57457201..57457324 26863196 MeRIP-seq:(Medium) rs1182921951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260084,Human_RBP_ID_8178655,Human_RBP_ID_26421431 91021 RMVar_ID_91021 Human_SNP_ID_502675335 m1A Human chr12 + 57459854 57459854 57459854 CCTGGGGGTCCTGGGGGTGCAATAAGCCCGGCACCCCTTCTCTTGCTTCCAGCTACCCCGCCTCA CCTGGGGGTCCTGGGGGTGCAATAAGCCCGGCCCCCCTTCTCTTGCTTCCAGCTACCCCGCCTCA A C GLI1 Ensembl:ENSG00000111087 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57459807..57459968 26863196 MeRIP-seq:(Medium) rs990190555 Functional Loss SNV dbSNP153 33..33 33 - - - 91022 RMVar_ID_91022 Human_SNP_ID_502683920 m1A Human chr12 - 57488176 57488176 57488176 CACGAGTACCTTCCGGGCCTACAGTGCTGATGAGCACCTCTGCTCTGCCCCGGGCTCTCCCGGCG CACGAGTACCTTCCGGGCCTACAGTGCTGATGGGCACCTCTGCTCTGCCCCGGGCTCTCCCGGCG T C ARHGAP9 Ensembl:ENSG00000123329 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:57488076..57488232 26863410 MeRIP-seq:(Medium) rs369180672 Functional Loss SNV dbSNP153 33..33 33 - - - 91023 RMVar_ID_91023 Human_SNP_ID_502684384 m1A Human chr12 + 57489523 57489523 57489523 CAGTGCGGAGAGCCCTGACTCACATTGACCACAGCTTGAGTCGTCAGAACTGTCCTTTCCTGGCT CAGTGCGGAGAGCCCTGACTCACATTGACCACGGCTTGAGTCGTCAGAACTGTCCTTTCCTGGCT A G MARS1 Ensembl:ENSG00000166986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57489473..57489574 26863196 MeRIP-seq:(Medium) rs1046282755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424713,Human_RBP_ID_878057,Human_RBP_ID_1270050,Human_RBP_ID_1475022,Human_RBP_ID_1798234,Human_RBP_ID_3409927,Human_RBP_ID_3941873,Human_RBP_ID_4234594,Human_RBP_ID_5170514,Human_RBP_ID_9255511,Human_RBP_ID_11994901,Human_RBP_ID_18434530,Human_RBP_ID_18630469,Human_RBP_ID_18975879,Human_RBP_ID_22437260 Human_Splice_Rec_1388310,Human_Splice_Rec_1388311,Human_Splice_Rec_1388350,Human_Splice_Rec_1388351,Human_Splice_Rec_1388361,Human_Splice_Rec_1388368,Human_Splice_Rec_1388374,Human_Splice_Rec_1388375,Human_Splice_Rec_1388416,Human_Splice_Rec_1388422,Human_Splice_Rec_1388423,Human_Splice_Rec_1388430,Human_Splice_Rec_1388431,Human_Splice_Rec_1388508,Human_Splice_Rec_1388509,Human_Splice_Rec_1388572,Human_Splice_Rec_1388573,Human_Splice_Rec_1388577 RMVar_hsa_circ_157657,RMVar_hsa_circ_77258,RMVar_hsa_circ_93971,RMVar_hsa_circ_127822,RMVar_hsa_circ_84649,RMVar_hsa_circ_157658,RMVar_hsa_circ_157659,RMVar_hsa_circ_112516,RMVar_hsa_circ_157656,RMVar_hsa_circ_76686,RMVar_hsa_circ_157660,RMVar_hsa_circ_157661,RMVar_hsa_circ_39745 91024 RMVar_ID_91024 Human_SNP_ID_502684603 m1A Human chr12 - 57490316 57490316 57490316 GCGGGGCTGGGCTGGGGCTGCTTTTGGAGGTAAGGCCGGAGAGCCAGGACACCTTGCTGTTTCAG GCGGGGCTGGGCTGGGGCTGCTTTTGGAGGTATGGCCGGAGAGCCAGGACACCTTGCTGTTTCAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57489780..57490315 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 91025 RMVar_ID_91025 Human_SNP_ID_502684693 m1A Human chr12 - 57490614 57490614 57490614 ACACTGGATTCTGCTGGGGCCGCAGCGGGGGCAAACTTTCTAGGCCCTTCTCCCAAGCAGTAACA ACACTGGATTCTGCTGGGGCCGCAGCGGGGGCGAACTTTCTAGGCCCTTCTCCCAAGCAGTAACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57490505..57490676 26863196 MeRIP-seq:(Medium) rs763613524 Functional Loss SNV dbSNP153 33..33 33 - - - 91026 RMVar_ID_91026 Human_SNP_ID_502687939 m1A Human chr12 - 57497100 57497098 57497101 TCCCAACCCCCTAACCACTTTGTACCATATTGAGTAGTGCTCCTTTTGTGTTACCCTGTCACTTA TCCCAACCCCCTAACCACTTTGTACCATATT___TAGTGCTCCTTTTGTGTTACCCTGTCACTTA ACTC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57497096..57497666 26863196 MeRIP-seq:(Medium) rs1321575356 Functional Loss DEL dbSNP153 32..34 33 - - - 91027 RMVar_ID_91027 Human_SNP_ID_502687943 m1A Human chr12 + 57497121 57497121 57497121 AGGAGCACTACTCAATATGGTACAAAGTGGTTAGGGGGTTGGGATACAAAAAAGACTGTGTGGGA AGGAGCACTACTCAATATGGTACAAAGTGGTTGGGGGGTTGGGATACAAAAAAGACTGTGTGGGA A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57497119..57497861 26863196 MeRIP-seq:(Medium) rs773828694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22572815 RMVar_hsa_circ_77258,RMVar_hsa_circ_93971,RMVar_hsa_circ_157658,RMVar_hsa_circ_157659,RMVar_hsa_circ_112516,RMVar_hsa_circ_105310,RMVar_hsa_circ_157661,RMVar_hsa_circ_123043,RMVar_hsa_circ_157663,RMVar_hsa_circ_95441,RMVar_hsa_circ_157662,RMVar_hsa_circ_113933,RMVar_hsa_circ_157664,RMVar_hsa_circ_157665 91028 RMVar_ID_91028 Human_SNP_ID_502687945 m1A Human chr12 - 57497127 57497127 57497127 CCATCTTCCCACACAGTCTTTTTTGTATCCCAACCCCCTAACCACTTTGTACCATATTGAGTAGT CCATCTTCCCACACAGTCTTTTTTGTATCCCAGCCCCCTAACCACTTTGTACCATATTGAGTAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57497122..57497526 26863196 MeRIP-seq:(Medium) rs1391116655 Functional Loss SNV dbSNP153 33..33 33 - - - 91029 RMVar_ID_91029 Human_SNP_ID_502692381 m1A Human chr12 - 57512814 57512814 57512814 AGATGTCAGCAGGGATCCCCGTGTCCTGGGCCATGTCCCCAAACACTCCCACACCGCGGCTCTTA AGATGTCAGCAGGGATCCCCGTGTCCTGGGCCGTGTCCCCAAACACTCCCACACCGCGGCTCTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57512766..57512912 26863196 MeRIP-seq:(Medium) rs1388819320 Functional Loss SNV dbSNP153 33..33 33 - - - 91030 RMVar_ID_91030 Human_SNP_ID_502692395 m1A Human chr12 + 57512856 57512856 57512856 CACGGGGATCCCTGCTGACATCTGGCGCTTCTATCTGCTGTACATTCGGCCTGAGGGCCAGGACA CACGGGGATCCCTGCTGACATCTGGCGCTTCTGTCTGCTGTACATTCGGCCTGAGGGCCAGGACA A G MARS1 Ensembl:ENSG00000166986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57512751..57512975 32194978 MeRIP-seq:(Medium) rs777332933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424738,Human_RBP_ID_754050,Human_RBP_ID_1475080,Human_RBP_ID_3409951,Human_RBP_ID_4257991,Human_RBP_ID_8068784,Human_RBP_ID_8380677,Human_RBP_ID_8783969,Human_RBP_ID_9255529,Human_RBP_ID_9278335,Human_RBP_ID_17239908,Human_RBP_ID_17472767,Human_RBP_ID_17823650,Human_RBP_ID_18262479,Human_RBP_ID_18630526,Human_RBP_ID_22794931,Human_RBP_ID_27423940 Human_miRNA_ID_1426082 RMVar_hsa_circ_15567,RMVar_hsa_circ_361972,RMVar_hsa_circ_94821,RMVar_hsa_circ_123367,RMVar_hsa_circ_157669,RMVar_hsa_circ_376396,RMVar_hsa_circ_373799,RMVar_hsa_circ_157675,RMVar_hsa_circ_157677,RMVar_hsa_circ_117871,RMVar_hsa_circ_157676,RMVar_hsa_circ_157674,RMVar_hsa_circ_346254,RMVar_hsa_circ_24304 91031 RMVar_ID_91031 Human_SNP_ID_502692885 m1A Human chr12 - 57514780 57514780 57514780 AGGGTGACATGGGCCAGCAGGCGCTGATCATCAGGGGTGAGCACCATCTCAGGCACATAGCCCCC AGGGTGACATGGGCCAGCAGGCGCTGATCATCGGGGGTGAGCACCATCTCAGGCACATAGCCCCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57514764..57514963 26863410 MeRIP-seq:(Medium) rs761661277 Functional Loss SNV dbSNP153 33..33 33 - - - 91032 RMVar_ID_91032 Human_SNP_ID_502692984 m1A Human chr12 - 57515037 57515037 57515037 CGCTTACCTACCTGTCAGCCTCACTGCCTTTAATCCGCTTCCAGGGCTCATTCACCTGAATATAT CGCTTACCTACCTGTCAGCCTCACTGCCTTTATTCCGCTTCCAGGGCTCATTCACCTGAATATAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57514935..57515036 26863196 MeRIP-seq:(Medium) rs1185022387 Functional Loss SNV dbSNP153 33..33 33 - - - 91033 RMVar_ID_91033 Human_SNP_ID_502693498 m1A Human chr12 + 57516571 57516571 57516571 GGGGAAACCCCCTGAAGCCCCTAAAGGCAAGAAGAAAAAGTAAAAGACCTTGGCTCATAGAAAGT GGGGAAACCCCCTGAAGCCCCTAAAGGCAAGACGAAAAAGTAAAAGACCTTGGCTCATAGAAAGT A C MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57516435..57516578 26863196 MeRIP-seq:(Medium) rs28382854 Functional Loss SNV dbSNP153,EGP,HGVD 33..33 33 - - - Human_RBP_ID_9365134,Human_RBP_ID_26909813 Human_Splice_Rec_1388590 Human_miRNA_ID_1744443 RMVar_hsa_circ_123367,RMVar_hsa_circ_157677 91034 RMVar_ID_91034 Human_SNP_ID_502693566 m1A Human chr12 + 57516783 57516783 57516783 CCACTTCTGGGAAAGGTGGGTAGTGTGGCCCAAGTGGGGGACTGATGCTCCCAATTGTTCATGCT CCACTTCTGGGAAAGGTGGGTAGTGTGGCCCAGGTGGGGGACTGATGCTCCCAATTGTTCATGCT A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57516733..57516831 32194978 MeRIP-seq:(Medium) rs755753113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3409960,Human_RBP_ID_5349858 91035 RMVar_ID_91035 Human_SNP_ID_502693634 m1A Human chr12 - 57516942 57516942 57516942 TGGAAAGCAGCGCATGAAGGAGAAAGAACAGGAGAATGAAAGGAAAGTGGCACAGCTAGCTGAAG TGGAAAGCAGCGCATGAAGGAGAAAGAACAGGGGAATGAAAGGAAAGTGGCACAGCTAGCTGAAG T C DDIT3 Ensembl:ENSG00000175197 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57516892..57516996 26863196 MeRIP-seq:(Medium) rs762002610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424762,Human_RBP_ID_1475135,Human_RBP_ID_3409961,Human_RBP_ID_22910763,Human_RBP_ID_23581727,Human_RBP_ID_24543087,Human_RBP_ID_26321654,Human_RBP_ID_26421439,Human_RBP_ID_27216979,Human_RBP_ID_27423951,Human_RBP_ID_27806760 91036 RMVar_ID_91036 Human_SNP_ID_502693809 m1A Human chr12 + 57517367 57517366 57517367 GTCCTCATACCAGGCTTCCAGCTCCCAGCTGGACAGTGTCCCGAAGGAGAAAGGCAATGACTCAG GTCCTCATACCAGGCTTCCAGCTCCCAGCTGG_CAGTGTCCCGAAGGAGAAAGGCAATGACTCAG GA G MARS1 Ensembl:ENSG00000166986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57517317..57517420 32194978 MeRIP-seq:(Medium) rs1279881449 Functional Loss DEL dbSNP153 33..33 33 - - - 91037 RMVar_ID_91037 Human_SNP_ID_502694635 m1A Human chr12 - 57520454 57520454 57520454 CGTATCATGTTAAAGATGAGCGGGTGGCAGCGACAGAGCCAAAATCAGAGCTGGAACCTGAGGAG CGTATCATGTTAAAGATGAGCGGGTGGCAGCGGCAGAGCCAAAATCAGAGCTGGAACCTGAGGAG T C DDIT3,AC022506.1 Ensembl:ENSG00000175197,Ensembl:ENSG00000285133 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57520369..57520455 26863196 MeRIP-seq:(Medium) rs1177621300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424767,Human_RBP_ID_1475154,Human_RBP_ID_4248185,Human_RBP_ID_5087278,Human_RBP_ID_6203657,Human_RBP_ID_22756376,Human_RBP_ID_26321656,Human_RBP_ID_27806763 91038 RMVar_ID_91038 Human_SNP_ID_502695382 m1A Human chr12 + 57522759 57522724 57522760 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA __________________________________GGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA AGGCGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGAC A MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1565659491 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_4234743 91039 RMVar_ID_91039 Human_SNP_ID_502695383 m1A Human chr12 + 57522759 57522726 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA _________________________________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1353184541 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4234743 91040 RMVar_ID_91040 Human_SNP_ID_502695389 m1A Human chr12 + 57522759 57522732 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGG___________________________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCTCCTGCGGCGGCGGCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1178329634 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_4234743 91041 RMVar_ID_91041 Human_SNP_ID_502695400 m1A Human chr12 + 57522759 57522738 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTG_____________________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCGGCGGCGGCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1372750937 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_4234743 91042 RMVar_ID_91042 Human_SNP_ID_502695404 m1A Human chr12 + 57522759 57522741 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGG__________________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCGGCGGCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs965627168 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_4234743 91043 RMVar_ID_91043 Human_SNP_ID_502695408 m1A Human chr12 + 57522759 57522744 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGG_______________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCGGCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1282780182 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_4234743 91044 RMVar_ID_91044 Human_SNP_ID_502695412 m1A Human chr12 + 57522779 57522746 57522779 GCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCAGTGCCTTCTGGGAACGGAAT _________________________________GCAGCCTGCGCAGTGCCTTCTGGGAACGGAAT GGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57522729..57522802 26863196 MeRIP-seq:(Medium) rs1358387921 Functional Loss DEL dbSNP153 1..33 33 - - - 91045 RMVar_ID_91045 Human_SNP_ID_502695417 m1A Human chr12 + 57522759 57522747 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGGCGG____________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCTGCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1472367540 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4234743 91046 RMVar_ID_91046 Human_SNP_ID_502695425 m1A Human chr12 + 57522759 57522750 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGGCGGCTG_________CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCGGCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1313046426 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4234743 91047 RMVar_ID_91047 Human_SNP_ID_502695427 m1A Human chr12 + 57522759 57522753 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGGCGGCTGCGG______CGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA GCAGCGA G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs1402174810 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4234743 91048 RMVar_ID_91048 Human_SNP_ID_502695437 m1A Human chr12 + 57522759 57522759 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGGCGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA A G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs181698936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4234743 91049 RMVar_ID_91049 Human_SNP_ID_502695494 m1A Human chr12 + 57522779 57522779 57522779 GCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCAGTGCCTTCTGGGAACGGAAT GCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCGGCAGCCTGCGCAGTGCCTTCTGGGAACGGAAT A G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57522729..57522802 26863196 MeRIP-seq:(Medium) rs1399989255 Functional Loss SNV dbSNP153 33..33 33 - - - 91050 RMVar_ID_91050 Human_SNP_ID_502695998 m1A Human chr12 + 57524335 57524335 57524335 AATGAATGGGGGCAATGAGAGCAGTGGAGCAGACAGAGCTGGGGGCCCTGTGGCCACATCTGTCC AATGAATGGGGGCAATGAGAGCAGTGGAGCAGGCAGAGCTGGGGGCCCTGTGGCCACATCTGTCC A G MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57524242..57524357 26863196 MeRIP-seq:(Medium) rs1281396067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111510,Human_RBP_ID_18975896 Human_Splice_Rec_1388674,Human_Splice_Rec_1388675,Human_Splice_Rec_1388684,Human_Splice_Rec_1388685,Human_Splice_Rec_1388690,Human_Splice_Rec_1388691,Human_Splice_Rec_1388696,Human_Splice_Rec_1388697,Human_Splice_Rec_1388704,Human_Splice_Rec_1388705,Human_Splice_Rec_1388727,Human_Splice_Rec_1388738,Human_Splice_Rec_1388739,Human_Splice_Rec_1388742,Human_Splice_Rec_1388743,Human_Splice_Rec_1388747 Human_miRNA_ID_2295706,Human_miRNA_ID_2469237,Human_miRNA_ID_2573782 RMVar_hsa_circ_120126,RMVar_hsa_circ_157679 91051 RMVar_ID_91051 Human_SNP_ID_502696363 m1A Human chr12 + 57525367 57525367 57525367 TCATTTATTGCAGGAGAGGGAGCGAGCCCCCAAATGTTCCACACTGTGTCCCCAGGGCCCCCCTC TCATTTATTGCAGGAGAGGGAGCGAGCCCCCACATGTTCCACACTGTGTCCCCAGGGCCCCCCTC A C MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57525355..57525457 26863196 MeRIP-seq:(Medium) rs1303430395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230083,Human_RBP_ID_18977543 Human_Splice_Rec_1388680,Human_Splice_Rec_1388710,Human_Splice_Rec_1388734 RMVar_hsa_circ_66071 91052 RMVar_ID_91052 Human_SNP_ID_502696364 m1A Human chr12 + 57525367 57525367 57525367 TCATTTATTGCAGGAGAGGGAGCGAGCCCCCAAATGTTCCACACTGTGTCCCCAGGGCCCCCCTC TCATTTATTGCAGGAGAGGGAGCGAGCCCCCAGATGTTCCACACTGTGTCCCCAGGGCCCCCCTC A G MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57525355..57525457 26863196 MeRIP-seq:(Medium) rs1303430395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230083,Human_RBP_ID_18977543 Human_Splice_Rec_1388680,Human_Splice_Rec_1388710,Human_Splice_Rec_1388734 RMVar_hsa_circ_66071 91053 RMVar_ID_91053 Human_SNP_ID_502696484 m1A Human chr12 - 57525613 57525613 57525613 GAGGGAGCATTGAGGCTGATAGCAGGTGGAGGAGGTGGGGCTGGAGAGGGGGCATTGCCCCTTGG GAGGGAGCATTGAGGCTGATAGCAGGTGGAGGTGGTGGGGCTGGAGAGGGGGCATTGCCCCTTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:57525576..57525650 26863196 MeRIP-seq:(Medium) rs200229613 Functional Loss SNV dbSNP153 33..33 33 - - - 91054 RMVar_ID_91054 Human_SNP_ID_502696499 m1A Human chr12 + 57525635 57525635 57525635 CAGCCCCACCTCCTCCACCTGCTATCAGCCTCAATGCTCCCTCATACAACTGGGGAGCTGCCCTC CAGCCCCACCTCCTCCACCTGCTATCAGCCTCGATGCTCCCTCATACAACTGGGGAGCTGCCCTC A G MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57525584..57525778 26863196 MeRIP-seq:(Medium) rs764731352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126910,Human_RBP_ID_17075143,Human_RBP_ID_17239925,Human_RBP_ID_17472774,Human_RBP_ID_17823677,Human_RBP_ID_18935494,Human_RBP_ID_19792611 RMVar_hsa_circ_66071 91055 RMVar_ID_91055 Human_SNP_ID_502696626 m1A Human chr12 + 57525900 57525900 57525900 CCTGGGGCCCCTGGGAGGGGCCCCCACGGTGGAGGGGCCTGGGGCACCCCCCTTCCTTGCTAGCA CCTGGGGCCCCTGGGAGGGGCCCCCACGGTGGGGGGGCCTGGGGCACCCCCCTTCCTTGCTAGCA A G MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57525851..57525926 26863196 MeRIP-seq:(Medium) rs1372021127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126913,Human_RBP_ID_17074905 RMVar_hsa_circ_66071 91056 RMVar_ID_91056 Human_SNP_ID_502696785 m1A Human chr12 + 57526242 57526242 57526242 CCTGCTGGGACTCCCCACCCCTGGCCCTTCCCACTCTGATGGAAGCTTTAACCTTTTGGGGTCAG CCTGCTGGGACTCCCCACCCCTGGCCCTTCCCCCTCTGATGGAAGCTTTAACCTTTTGGGGTCAG A C MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57526191..57526618 32194978 MeRIP-seq:(Medium) rs757745875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418399,Human_RBP_ID_5127183,Human_RBP_ID_17075149,Human_RBP_ID_18935502 RMVar_hsa_circ_66071 91057 RMVar_ID_91057 Human_SNP_ID_502697943 m1A Human chr12 + 57529212 57529210 57529213 CCGGGCCCGCCCTGGCCGTCCTGCCAAAAACAAGAGGAGGAAACTGGCCCCATAGCAGCCATACC CCGGGCCCGCCCTGGCCGTCCTGCCAAAAAC___AGGAGGAAACTGGCCCCATAGCAGCCATACC CAAG C MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57529155..57529263 26863196 MeRIP-seq:(Medium) rs980732118 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_19792703 Human_Splice_Rec_1388724,Human_Splice_Rec_1388766,Human_Splice_Rec_1388778 Human_miRNA_ID_2662547,Human_miRNA_ID_2681000 RMVar_hsa_circ_122667,RMVar_hsa_circ_104215,RMVar_hsa_circ_157680,RMVar_hsa_circ_157681 91058 RMVar_ID_91058 Human_SNP_ID_502697945 m1A Human chr12 + 57529212 57529212 57529212 CCGGGCCCGCCCTGGCCGTCCTGCCAAAAACAAGAGGAGGAAACTGGCCCCATAGCAGCCATACC CCGGGCCCGCCCTGGCCGTCCTGCCAAAAACAGGAGGAGGAAACTGGCCCCATAGCAGCCATACC A G MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57529155..57529263 26863196 MeRIP-seq:(Medium) rs199628867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19792703 Human_Splice_Rec_1388724,Human_Splice_Rec_1388766,Human_Splice_Rec_1388778 Human_miRNA_ID_2662547,Human_miRNA_ID_2681000 RMVar_hsa_circ_122667,RMVar_hsa_circ_104215,RMVar_hsa_circ_157680,RMVar_hsa_circ_157681 91059 RMVar_ID_91059 Human_SNP_ID_502697946 m1A Human chr12 + 57529212 57529212 57529212 CCGGGCCCGCCCTGGCCGTCCTGCCAAAAACAAGAGGAGGAAACTGGCCCCATAGCAGCCATACC CCGGGCCCGCCCTGGCCGTCCTGCCAAAAACATGAGGAGGAAACTGGCCCCATAGCAGCCATACC A T MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57529155..57529263 26863196 MeRIP-seq:(Medium) rs199628867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19792703 Human_Splice_Rec_1388724,Human_Splice_Rec_1388766,Human_Splice_Rec_1388778 Human_miRNA_ID_2662547,Human_miRNA_ID_2681000 RMVar_hsa_circ_122667,RMVar_hsa_circ_104215,RMVar_hsa_circ_157680,RMVar_hsa_circ_157681 91060 RMVar_ID_91060 Human_SNP_ID_502699452 m1A Human chr12 - 57534065 57534065 57534065 GCGCCTACTACTGCAGCTGGAAGCAACAAAGAACAGCAAAGGGGGATCAGGGGGAAAAACCACTG GCGCCTACTACTGCAGCTGGAAGCAACAAAGATCAGCAAAGGGGGATCAGGGGGAAAAACCACTG T A DCTN2 Ensembl:ENSG00000175203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57534014..57534140 26863196 MeRIP-seq:(Medium) rs374514646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1388792,Human_Splice_Rec_1388822,Human_Splice_Rec_1388848,Human_Splice_Rec_1388876,Human_Splice_Rec_1388894,Human_Splice_Rec_1388922,Human_Splice_Rec_1388946,Human_Splice_Rec_1388976,Human_Splice_Rec_1389008,Human_Splice_Rec_1389018 RMVar_hsa_circ_84786,RMVar_hsa_circ_106836,RMVar_hsa_circ_125355,RMVar_hsa_circ_108794,RMVar_hsa_circ_100953,RMVar_hsa_circ_102937,RMVar_hsa_circ_93357,RMVar_hsa_circ_157684,RMVar_hsa_circ_157688,RMVar_hsa_circ_84042,RMVar_hsa_circ_157689,RMVar_hsa_circ_157686,RMVar_hsa_circ_157687,RMVar_hsa_circ_157685,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_48243,RMVar_hsa_circ_157697,RMVar_hsa_circ_14867,RMVar_hsa_circ_277537,RMVar_hsa_circ_372411,RMVar_hsa_circ_82098,RMVar_hsa_circ_157698,RMVar_hsa_circ_157699 91061 RMVar_ID_91061 Human_SNP_ID_502699543 m1A Human chr12 + 57534363 57534363 57534363 GCATCTGGTCCCAGCAGCTTCTCCAGGTGGGAAGCAACCAGCTGCTGCTTCAGGGCTGCCAGCTG GCATCTGGTCCCAGCAGCTTCTCCAGGTGGGAGGCAACCAGCTGCTGCTTCAGGGCTGCCAGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57534276..57534475 32194978 MeRIP-seq:(Medium) rs779008759 Functional Loss SNV dbSNP153 33..33 33 - - - 91062 RMVar_ID_91062 Human_SNP_ID_502699561 m1A Human chr12 - 57534435 57534435 57534435 CTTTTTTCATACTAGACGACAGTGAAGGAGTCAGCCACAGAGGAGAAGCTGACCCCTGTGTTGCT CTTTTTTCATACTAGACGACAGTGAAGGAGTCGGCCACAGAGGAGAAGCTGACCCCTGTGTTGCT T C DCTN2 Ensembl:ENSG00000175203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr12:57534248..57534494;chr12:57534335..57534435 26863196,26863410 MeRIP-seq:(Medium) rs1194249747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424814,Human_RBP_ID_874797,Human_RBP_ID_1475186,Human_RBP_ID_3941899,Human_RBP_ID_9344588,Human_RBP_ID_18977551,Human_RBP_ID_22645088,Human_RBP_ID_22794957,Human_RBP_ID_25015597,Human_RBP_ID_26321657 Human_Splice_Rec_1388790,Human_Splice_Rec_1388820,Human_Splice_Rec_1388846,Human_Splice_Rec_1388874,Human_Splice_Rec_1388892,Human_Splice_Rec_1388920,Human_Splice_Rec_1388944,Human_Splice_Rec_1388974,Human_Splice_Rec_1389006,Human_Splice_Rec_1389016,Human_Splice_Rec_1389026,Human_Splice_Rec_1389034 Human_miRNA_ID_2454156 RMVar_hsa_circ_84786,RMVar_hsa_circ_106836,RMVar_hsa_circ_125355,RMVar_hsa_circ_108794,RMVar_hsa_circ_100953,RMVar_hsa_circ_102937,RMVar_hsa_circ_93357,RMVar_hsa_circ_157684,RMVar_hsa_circ_157688,RMVar_hsa_circ_157686,RMVar_hsa_circ_157687,RMVar_hsa_circ_157685,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_48243,RMVar_hsa_circ_157697,RMVar_hsa_circ_14867,RMVar_hsa_circ_277537,RMVar_hsa_circ_372411,RMVar_hsa_circ_82098,RMVar_hsa_circ_157698,RMVar_hsa_circ_157699 91063 RMVar_ID_91063 Human_SNP_ID_502702217 m1A Human chr12 - 57546093 57546093 57546093 GGTTGGGTGGTCACTGCTTCTACCTGCAGGCCAGGAATGAGCCAGATGTTTATGAAACTAGCGAC GGTTGGGTGGTCACTGCTTCTACCTGCAGGCCGGGAATGAGCCAGATGTTTATGAAACTAGCGAC T C DCTN2 Ensembl:ENSG00000175203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57546076..57546151 26863196 MeRIP-seq:(Medium) rs778165740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22039992 Human_Splice_Rec_1388782,Human_Splice_Rec_1388783,Human_Splice_Rec_1388808,Human_Splice_Rec_1388809,Human_Splice_Rec_1388838,Human_Splice_Rec_1388839,Human_Splice_Rec_1388862,Human_Splice_Rec_1388863,Human_Splice_Rec_1388910,Human_Splice_Rec_1388911,Human_Splice_Rec_1388964,Human_Splice_Rec_1388965,Human_Splice_Rec_1388992,Human_Splice_Rec_1388993,Human_Splice_Rec_1389036,Human_Splice_Rec_1389037,Human_Splice_Rec_1389052,Human_Splice_Rec_1389053,Human_Splice_Rec_1389056,Human_Splice_Rec_1389057 Human_miRNA_ID_2083622 RMVar_hsa_circ_84786,RMVar_hsa_circ_100953,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_83739,RMVar_hsa_circ_157701 91064 RMVar_ID_91064 Human_SNP_ID_502702221 m1A Human chr12 - 57546098 57546098 57546098 AGTGAGGTTGGGTGGTCACTGCTTCTACCTGCAGGCCAGGAATGAGCCAGATGTTTATGAAACTA AGTGAGGTTGGGTGGTCACTGCTTCTACCTGCCGGCCAGGAATGAGCCAGATGTTTATGAAACTA T G DCTN2 Ensembl:ENSG00000175203 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57546026..57546167 26863410 MeRIP-seq:(Medium) rs1322897633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_878355,Human_RBP_ID_22039992,Human_RBP_ID_22538775 Human_Splice_Rec_1388783,Human_Splice_Rec_1388809,Human_Splice_Rec_1388839,Human_Splice_Rec_1388863,Human_Splice_Rec_1388911,Human_Splice_Rec_1388965,Human_Splice_Rec_1388993,Human_Splice_Rec_1389037,Human_Splice_Rec_1389053,Human_Splice_Rec_1389057 RMVar_hsa_circ_100953,RMVar_hsa_circ_157682 91065 RMVar_ID_91065 Human_SNP_ID_502702522 m1A Human chr12 - 57547124 57547124 57547124 TTAGCCCGGGACCCGAACCCAGCCTCTCCCCTACCCGAACACCGGCCCCGGCTCCACCGAGGCCC TTAGCCCGGGACCCGAACCCAGCCTCTCCCCTGCCCGAACACCGGCCCCGGCTCCACCGAGGCCC T C DCTN2 Ensembl:ENSG00000175203 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:57547032..57547156 26863410 MeRIP-seq:(Medium) rs932239744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424818,Human_RBP_ID_811314,Human_RBP_ID_4258055,Human_RBP_ID_5437893,Human_RBP_ID_5462015,Human_RBP_ID_22436032,Human_RBP_ID_22906673,Human_RBP_ID_26806917 Human_Splice_Rec_1388781,Human_Splice_Rec_1388807,Human_Splice_Rec_1388837,Human_Splice_Rec_1388861,Human_Splice_Rec_1388909,Human_Splice_Rec_1388963,Human_Splice_Rec_1388991,Human_Splice_Rec_1389019,Human_Splice_Rec_1389035,Human_Splice_Rec_1389051,Human_Splice_Rec_1389055,Human_Splice_Rec_1389059 RMVar_hsa_circ_100953,RMVar_hsa_circ_157682 91066 RMVar_ID_91066 Human_SNP_ID_502702532 m1A Human chr12 - 57547146 57547146 57547146 TGCCGCTCCCTTTGCCGCCGCCTTAGCCCGGGACCCGAACCCAGCCTCTCCCCTACCCGAACACC TGCCGCTCCCTTTGCCGCCGCCTTAGCCCGGGTCCCGAACCCAGCCTCTCCCCTACCCGAACACC T A DCTN2 Ensembl:ENSG00000175203 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:57547046..57547156 26863410 MeRIP-seq:(Medium) rs542746263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424819,Human_RBP_ID_754262,Human_RBP_ID_811314,Human_RBP_ID_5437893,Human_RBP_ID_5462015,Human_RBP_ID_8380737,Human_RBP_ID_22436032 RMVar_hsa_circ_100953,RMVar_hsa_circ_157682 91067 RMVar_ID_91067 Human_SNP_ID_502741890 m1A Human chr12 - 57694202 57694202 57694202 TCAGACTTGCGGGTAACAGGAGTCCCAGAAGCAGCAGTCCTAACAAACTGGACAGCAGCGTTTCC TCAGACTTGCGGGTAACAGGAGTCCCAGAAGCGGCAGTCCTAACAAACTGGACAGCAGCGTTTCC T C AC025165.2 Ensembl:ENSG00000257342 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:57694151..57694363;chr12:57694151..57694367 26863196 MeRIP-seq:(Medium) rs1463947638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1390156 91068 RMVar_ID_91068 Human_SNP_ID_502746869 m1A Human chr12 + 57715773 57715773 57715773 ATCCTTTCTGTCCTGGCAGTTCCTCTGTGACGAGGGTGCAGGTATCTCTGGGGACTACATCGATC ATCCTTTCTGTCCTGGCAGTTCCTCTGTGACGGGGGTGCAGGTATCTCTGGGGACTACATCGATC A G OS9 Ensembl:ENSG00000135506 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57696276..57715975 32194978 MeRIP-seq:(Medium) rs553683392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3410034,Human_RBP_ID_6203914,Human_RBP_ID_8380773,Human_RBP_ID_22436600,Human_RBP_ID_22756022 Human_Splice_Rec_1389856,Human_Splice_Rec_1389890,Human_Splice_Rec_1389922,Human_Splice_Rec_1389936,Human_Splice_Rec_1389962,Human_Splice_Rec_1390002,Human_Splice_Rec_1390026,Human_Splice_Rec_1390048,Human_Splice_Rec_1390068,Human_Splice_Rec_1390076,Human_Splice_Rec_1390086,Human_Splice_Rec_1390118 RMVar_hsa_circ_19152,RMVar_hsa_circ_312133,RMVar_hsa_circ_368245,RMVar_hsa_circ_40213,RMVar_hsa_circ_83928,RMVar_hsa_circ_157729,RMVar_hsa_circ_157730,RMVar_hsa_circ_157732 91069 RMVar_ID_91069 Human_SNP_ID_502747179 m1A Human chr12 + 57716499 57716499 57716499 TGAGCCAGAGGACCAGGCCCCAGGAGGGGAGGAGGTGCCGGCTGAGGTGAGACCAGCTGCCTCAG TGAGCCAGAGGACCAGGCCCCAGGAGGGGAGGGGGTGCCGGCTGAGGTGAGACCAGCTGCCTCAG A G OS9 Ensembl:ENSG00000135506 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57716340..57716750 32194978 MeRIP-seq:(Medium) rs1343436800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229962,Human_RBP_ID_755707,Human_RBP_ID_18975918,Human_RBP_ID_22436604,Human_RBP_ID_22756024,Human_RBP_ID_26321674 Human_Splice_Rec_1389860,Human_Splice_Rec_1389861,Human_Splice_Rec_1389894,Human_Splice_Rec_1389895,Human_Splice_Rec_1389940,Human_Splice_Rec_1389941,Human_Splice_Rec_1389966,Human_Splice_Rec_1389967,Human_Splice_Rec_1390006,Human_Splice_Rec_1390007,Human_Splice_Rec_1390030,Human_Splice_Rec_1390031,Human_Splice_Rec_1390052,Human_Splice_Rec_1390053,Human_Splice_Rec_1390090,Human_Splice_Rec_1390091,Human_Splice_Rec_1390120,Human_Splice_Rec_1390121,Human_Splice_Rec_1390134,Human_Splice_Rec_1390135,Human_Splice_Rec_1390142,Human_Splice_Rec_1390143,Human_Splice_Rec_1390147 RMVar_hsa_circ_19152,RMVar_hsa_circ_368245,RMVar_hsa_circ_40213,RMVar_hsa_circ_157730 91070 RMVar_ID_91070 Human_SNP_ID_502747180 m1A Human chr12 + 57716499 57716499 57716499 TGAGCCAGAGGACCAGGCCCCAGGAGGGGAGGAGGTGCCGGCTGAGGTGAGACCAGCTGCCTCAG TGAGCCAGAGGACCAGGCCCCAGGAGGGGAGGTGGTGCCGGCTGAGGTGAGACCAGCTGCCTCAG A T OS9 Ensembl:ENSG00000135506 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57716340..57716750 32194978 MeRIP-seq:(Medium) rs1343436800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229962,Human_RBP_ID_755707,Human_RBP_ID_18975918,Human_RBP_ID_22436604,Human_RBP_ID_22756024,Human_RBP_ID_26321674 Human_Splice_Rec_1389860,Human_Splice_Rec_1389861,Human_Splice_Rec_1389894,Human_Splice_Rec_1389895,Human_Splice_Rec_1389940,Human_Splice_Rec_1389941,Human_Splice_Rec_1389966,Human_Splice_Rec_1389967,Human_Splice_Rec_1390006,Human_Splice_Rec_1390007,Human_Splice_Rec_1390030,Human_Splice_Rec_1390031,Human_Splice_Rec_1390052,Human_Splice_Rec_1390053,Human_Splice_Rec_1390090,Human_Splice_Rec_1390091,Human_Splice_Rec_1390120,Human_Splice_Rec_1390121,Human_Splice_Rec_1390134,Human_Splice_Rec_1390135,Human_Splice_Rec_1390142,Human_Splice_Rec_1390143,Human_Splice_Rec_1390147 RMVar_hsa_circ_19152,RMVar_hsa_circ_368245,RMVar_hsa_circ_40213,RMVar_hsa_circ_157730 91071 RMVar_ID_91071 Human_SNP_ID_502747657 m1A Human chr12 + 57718129 57718129 57718129 TCTCTGTTGAAACCCCAACTGTCTTTCTCCCCACTCCCTACCCACCCAGGGGAAGCCAAATATAG TCTCTGTTGAAACCCCAACTGTCTTTCTCCCCGCTCCCTACCCACCCAGGGGAAGCCAAATATAG A G OS9 Ensembl:ENSG00000135506 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57718126..57718150 32194978 MeRIP-seq:(Medium) rs1389828666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36740 RMVar_hsa_circ_19152,RMVar_hsa_circ_368245,RMVar_hsa_circ_157730 91072 RMVar_ID_91072 Human_SNP_ID_502748200 m1A Human chr12 - 57720079 57720079 57720079 TCAGGATCCTCCTCTTAGAGGGGGAGACACACAGGGAAACACAAAGCAGAGGCGTGACTCCAGGG TCAGGATCCTCCTCTTAGAGGGGGAGACACACTGGGAAACACAAAGCAGAGGCGTGACTCCAGGG T A AC025165.2 Ensembl:ENSG00000257342 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57720076..57720298 32194978 MeRIP-seq:(Medium) rs775803603 Functional Loss SNV dbSNP153 33..33 33 - - - 91073 RMVar_ID_91073 Human_SNP_ID_502748375 m1A Human chr12 - 57720507 57720507 57720507 TCGGGGGTAGAAGCCTCTTACCAAGATATTGAAGAAGATCTCCTTGAGGTTTCTCGTGTCCTCAT TCGGGGGTAGAAGCCTCTTACCAAGATATTGAGGAAGATCTCCTTGAGGTTTCTCGTGTCCTCAT T C AC025165.2 Ensembl:ENSG00000257342 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57720389..57720525 26863196 MeRIP-seq:(Medium) rs759886836 Functional Loss SNV dbSNP153 33..33 33 - - - 91074 RMVar_ID_91074 Human_SNP_ID_502748494 m1A Human chr12 + 57720902 57720902 57720902 TGGGGAGGGCACAGGGGACCTGGACGAATTTGACTTCTGAGACCAACACTACACTTGACCCTTCA TGGGGAGGGCACAGGGGACCTGGACGAATTTGGCTTCTGAGACCAACACTACACTTGACCCTTCA A G OS9 Ensembl:ENSG00000135506 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:57720852..57720972;chr12:57720852..57721207 26863196 MeRIP-seq:(Medium) rs1198458511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18630656,Human_RBP_ID_22176224,Human_RBP_ID_26909892,Human_RBP_ID_27217052,Human_RBP_ID_27558184 Human_miRNA_ID_2061545 RMVar_hsa_circ_101715,RMVar_hsa_circ_157733 91075 RMVar_ID_91075 Human_SNP_ID_502748519 m1A Human chr12 + 57720975 57720975 57720975 AGACTCTTCCTGGACTGGCTTGCCTCCTCCCCACCTCCCCACCCTGGAACCCCTGAGGGCCAAAC AGACTCTTCCTGGACTGGCTTGCCTCCTCCCCCCCTCCCCACCCTGGAACCCCTGAGGGCCAAAC A C OS9 Ensembl:ENSG00000135506 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57720926..57721025 32194978 MeRIP-seq:(Medium) rs867135512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228994,Human_RBP_ID_424937,Human_RBP_ID_753702,Human_RBP_ID_810465,Human_RBP_ID_876651,Human_RBP_ID_5112141,Human_RBP_ID_9366585,Human_RBP_ID_17357259,Human_RBP_ID_22436612,Human_RBP_ID_22906711,Human_RBP_ID_27424021 Human_miRNA_ID_842066,Human_miRNA_ID_1417961,Human_miRNA_ID_1701872,Human_miRNA_ID_2367445,Human_miRNA_ID_2725958,Human_miRNA_ID_2725959,Human_miRNA_ID_3015240 RMVar_hsa_circ_101715,RMVar_hsa_circ_157733 91076 RMVar_ID_91076 Human_SNP_ID_502748581 m1A Human chr12 + 57721307 57721307 57721307 ACACTTAGCAGGCACTGAGCAAGCAGGCCCCCACCTGCCCTTAGTGATGTTTGGAGTCGTTTTAC ACACTTAGCAGGCACTGAGCAAGCAGGCCCCCCCCTGCCCTTAGTGATGTTTGGAGTCGTTTTAC A C OS9 Ensembl:ENSG00000135506 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57720426..57721425 32194978 MeRIP-seq:(Medium) rs1049976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424945,Human_RBP_ID_4235225,Human_RBP_ID_18630660,Human_RBP_ID_26421460 Human_miRNA_ID_1417963,Human_miRNA_ID_1701874 RMVar_hsa_circ_101715,RMVar_hsa_circ_157733 91077 RMVar_ID_91077 Human_SNP_ID_502749776 m1A Human chr12 - 57726358 57726355 57726359 ACACAAACTCACCTCCCTCTCCCCAACGAGGCATGGAGACCCCAGCTCAACACGCCCCCTCTCCA ACACAAACTCACCTCCCTCTCCCCAACGAGG____GAGACCCCAGCTCAACACGCCCCCTCTCCA CCATG C AGAP2 Ensembl:ENSG00000135439 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57726307..57726386 26863196 MeRIP-seq:(Medium) rs577107321 Functional Loss DEL dbSNP153 32..35 33 - - - 91078 RMVar_ID_91078 Human_SNP_ID_502753293 m1A Human chr12 + 57737755 57737755 57737755 CTGCCGGTGCCAGGGTGCGGAGAGGATGAGCCAGGGATGCCGCCGCCCGCCCGGCCTTCGGGCTC CTGCCGGTGCCAGGGTGCGGAGAGGATGAGCCGGGGATGCCGCCGCCCGCCCGGCCTTCGGGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57737682..57737770 26863410 MeRIP-seq:(Medium) rs991468958 Functional Loss SNV dbSNP153 33..33 33 - - - 91079 RMVar_ID_91079 Human_SNP_ID_502756228 m1A Human chr12 - 57748221 57748221 57748221 AACAAAGAAATAATGGTCTTTTTTTTTTTTTTAATGTTTCTTCCTCTGTTTGGCTTTGCCATTGT AACAAAGAAATAATGGTCTTTTTTTTTTTTTTTATGTTTCTTCCTCTGTTTGGCTTTGCCATTGT T A CDK4 Ensembl:ENSG00000135446 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1238908150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345918,Human_RBP_ID_3410051,Human_RBP_ID_6203959,Human_RBP_ID_8380791,Human_RBP_ID_18630673,Human_RBP_ID_24467239 91080 RMVar_ID_91080 Human_SNP_ID_502756229 m1A Human chr12 - 57748221 57748221 57748221 AACAAAGAAATAATGGTCTTTTTTTTTTTTTTAATGTTTCTTCCTCTGTTTGGCTTTGCCATTGT AACAAAGAAATAATGGTCTTTTTTTTTTTTTTGATGTTTCTTCCTCTGTTTGGCTTTGCCATTGT T C CDK4 Ensembl:ENSG00000135446 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1238908150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345918,Human_RBP_ID_3410051,Human_RBP_ID_6203959,Human_RBP_ID_8380791,Human_RBP_ID_18630673,Human_RBP_ID_24467239 91081 RMVar_ID_91081 Human_SNP_ID_502756283 m1A Human chr12 - 57748494 57748494 57748494 GAGCAATGGAGTGGCTGCCATGGAAGGAAGAAAAGCTGCCATTTCCCTTCTGGACACTGAGAGGG GAGCAATGGAGTGGCTGCCATGGAAGGAAGAAGAGCTGCCATTTCCCTTCTGGACACTGAGAGGG T C CDK4 Ensembl:ENSG00000135446 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746950724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424999,Human_RBP_ID_993754,Human_RBP_ID_1358176,Human_RBP_ID_1475242,Human_RBP_ID_1798335,Human_RBP_ID_4258127,Human_RBP_ID_11996448,Human_RBP_ID_17472826,Human_RBP_ID_18975920,Human_RBP_ID_23568342,Human_RBP_ID_26418655,Human_RBP_ID_26909906,Human_RBP_ID_27217073 91082 RMVar_ID_91082 Human_SNP_ID_502756302 m1A Human chr12 - 57748541 57748541 57748541 AGCTCTGCAGCACTCTTATCTACATAAGGATGAAGGTAATCCGGAGTGAGCAATGGAGTGGCTGC AGCTCTGCAGCACTCTTATCTACATAAGGATGGAGGTAATCCGGAGTGAGCAATGGAGTGGCTGC T C CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57748320..57748575 32194978 MeRIP-seq:(Medium) rs771234928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424999,Human_RBP_ID_993755,Human_RBP_ID_1475244,Human_RBP_ID_1798336,Human_RBP_ID_8068797,Human_RBP_ID_9019032,Human_RBP_ID_11996452,Human_RBP_ID_17243766,Human_RBP_ID_17823822,Human_RBP_ID_18630675,Human_RBP_ID_22756036,Human_RBP_ID_23568343,Human_RBP_ID_27631409 Human_Splice_Rec_1390380,Human_Splice_Rec_1390392,Human_Splice_Rec_1390396,Human_Splice_Rec_1390402,Human_Splice_Rec_1390414,Human_Splice_Rec_1390426 Clinvar_Rec_515 RMVar_hsa_circ_157740,RMVar_hsa_circ_378849 91083 RMVar_ID_91083 Human_SNP_ID_502756303 m1A Human chr12 - 57748541 57748541 57748541 AGCTCTGCAGCACTCTTATCTACATAAGGATGAAGGTAATCCGGAGTGAGCAATGGAGTGGCTGC AGCTCTGCAGCACTCTTATCTACATAAGGATGCAGGTAATCCGGAGTGAGCAATGGAGTGGCTGC T G CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57748320..57748575 32194978 MeRIP-seq:(Medium) rs771234928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424999,Human_RBP_ID_993755,Human_RBP_ID_1475244,Human_RBP_ID_1798336,Human_RBP_ID_8068797,Human_RBP_ID_9019032,Human_RBP_ID_11996452,Human_RBP_ID_17243766,Human_RBP_ID_17823822,Human_RBP_ID_18630675,Human_RBP_ID_22756036,Human_RBP_ID_23568343,Human_RBP_ID_27631409 Human_Splice_Rec_1390380,Human_Splice_Rec_1390392,Human_Splice_Rec_1390396,Human_Splice_Rec_1390402,Human_Splice_Rec_1390414,Human_Splice_Rec_1390426 Clinvar_Rec_515 RMVar_hsa_circ_157740,RMVar_hsa_circ_378849 91084 RMVar_ID_91084 Human_SNP_ID_502756593 m1A Human chr12 - 57749299 57749299 57749299 CCTGTCCCCCACAGCCTGATTGGGCTGCCTCCAGAGGATGACTGGCCTCGAGATGTATCCCTGCC CCTGTCCCCCACAGCCTGATTGGGCTGCCTCCCGAGGATGACTGGCCTCGAGATGTATCCCTGCC T G CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57749171..57749525 26863410 MeRIP-seq:(Medium) rs368081942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425013,Human_RBP_ID_878461,Human_RBP_ID_993759,Human_RBP_ID_1475249,Human_RBP_ID_6203970,Human_RBP_ID_8784007,Human_RBP_ID_11996468,Human_RBP_ID_17650458,Human_RBP_ID_17823826,Human_RBP_ID_22436037,Human_RBP_ID_23125762,Human_RBP_ID_23568348 Human_Splice_Rec_1390378,Human_Splice_Rec_1390390,Human_Splice_Rec_1390394,Human_Splice_Rec_1390400,Human_Splice_Rec_1390412,Human_Splice_Rec_1390424,Human_Splice_Rec_1390436,Human_Splice_Rec_1390448,Human_Splice_Rec_1390458 Human_miRNA_ID_2475808,Human_miRNA_ID_2790942,Human_miRNA_ID_2793036,Human_miRNA_ID_2961593 Clinvar_Rec_516 RMVar_hsa_circ_100363,RMVar_hsa_circ_157740,RMVar_hsa_circ_378849,RMVar_hsa_circ_275818,RMVar_hsa_circ_157741,RMVar_hsa_circ_157742 91085 RMVar_ID_91085 Human_SNP_ID_502757267 m1A Human chr12 - 57751273 57751273 57751273 GAGATCAAGGTAACCCTGGTGTTTGAGCATGTAGACCAGGACCTAAGGACATATCTGGACAAGGC GAGATCAAGGTAACCCTGGTGTTTGAGCATGTGGACCAGGACCTAAGGACATATCTGGACAAGGC T C CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57750858..57751371 32194978 MeRIP-seq:(Medium) rs754092304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425034,Human_RBP_ID_1475267,Human_RBP_ID_1798349,Human_RBP_ID_3410061,Human_RBP_ID_5111515,Human_RBP_ID_5170526,Human_RBP_ID_6203986,Human_RBP_ID_8784013,Human_RBP_ID_11996566,Human_RBP_ID_18630688,Human_RBP_ID_23568354,Human_RBP_ID_26418665,Human_RBP_ID_26805873,Human_RBP_ID_26909918 Human_Splice_Rec_1390370,Human_Splice_Rec_1390371,Human_Splice_Rec_1390384,Human_Splice_Rec_1390416,Human_Splice_Rec_1390417,Human_Splice_Rec_1390430,Human_Splice_Rec_1390440,Human_Splice_Rec_1390441,Human_Splice_Rec_1390452,Human_Splice_Rec_1390453,Human_Splice_Rec_1390462,Human_Splice_Rec_1390463,Human_Splice_Rec_1390468,Human_Splice_Rec_1390469,Human_Splice_Rec_1390475,Human_Splice_Rec_1390480,Human_Splice_Rec_1390481,Human_Splice_Rec_1390486 Human_miRNA_ID_2149000 RMVar_hsa_circ_105605,RMVar_hsa_circ_122469,RMVar_hsa_circ_113095,RMVar_hsa_circ_157746,RMVar_hsa_circ_157747,RMVar_hsa_circ_157745 91086 RMVar_ID_91086 Human_SNP_ID_502757368 m1A Human chr12 + 57751571 57751571 57751571 AGTAAAGCCACCTCACGAACTGTGCTGATGGGAAGGCCTCCTCCACCTCCTCCTCCATTGGGGAC AGTAAAGCCACCTCACGAACTGTGCTGATGGGGAGGCCTCCTCCACCTCCTCCTCCATTGGGGAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57751520..57751750 26863196 MeRIP-seq:(Medium) rs1060504383 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_517 91087 RMVar_ID_91087 Human_SNP_ID_502757371 m1A Human chr12 - 57751577 57751574 57751577 GTGAGAGTCCCCAATGGAGGAGGAGGTGGAGGAGGCCTTCCCATCAGCACAGTTCGTGAGGTGGC GTGAGAGTCCCCAATGGAGGAGGAGGTGGAGG___CCTTCCCATCAGCACAGTTCGTGAGGTGGC GCCT G CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57751526..57751750 26863196 MeRIP-seq:(Medium) rs1555201374 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_34772,Human_RBP_ID_425037,Human_RBP_ID_753680,Human_RBP_ID_878468,Human_RBP_ID_993764,Human_RBP_ID_1475276,Human_RBP_ID_1798352,Human_RBP_ID_2345922,Human_RBP_ID_4246176,Human_RBP_ID_6203987,Human_RBP_ID_8247774,Human_RBP_ID_9019037,Human_RBP_ID_17823833,Human_RBP_ID_19793366,Human_RBP_ID_22794978,Human_RBP_ID_23568355,Human_RBP_ID_26909920,Human_RBP_ID_27217085 Human_Splice_Rec_1390369,Human_Splice_Rec_1390383,Human_Splice_Rec_1390405,Human_Splice_Rec_1390429,Human_Splice_Rec_1390438,Human_Splice_Rec_1390439,Human_Splice_Rec_1390451,Human_Splice_Rec_1390461,Human_Splice_Rec_1390467,Human_Splice_Rec_1390479,Human_Splice_Rec_1390485 Clinvar_Rec_518 RMVar_hsa_circ_122469,RMVar_hsa_circ_113095,RMVar_hsa_circ_157746,RMVar_hsa_circ_157745 91088 RMVar_ID_91088 Human_SNP_ID_502757372 m1A Human chr12 - 57751577 57751577 57751577 GTGAGAGTCCCCAATGGAGGAGGAGGTGGAGGAGGCCTTCCCATCAGCACAGTTCGTGAGGTGGC GTGAGAGTCCCCAATGGAGGAGGAGGTGGAGGCGGCCTTCCCATCAGCACAGTTCGTGAGGTGGC T G CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57751526..57751750 26863196 MeRIP-seq:(Medium) rs863224320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34772,Human_RBP_ID_425037,Human_RBP_ID_753680,Human_RBP_ID_878468,Human_RBP_ID_993764,Human_RBP_ID_1475276,Human_RBP_ID_1798352,Human_RBP_ID_2345922,Human_RBP_ID_4246176,Human_RBP_ID_6203987,Human_RBP_ID_8247774,Human_RBP_ID_9019037,Human_RBP_ID_17823833,Human_RBP_ID_19793366,Human_RBP_ID_22794978,Human_RBP_ID_23568355,Human_RBP_ID_26909920,Human_RBP_ID_27217085 Human_Splice_Rec_1390369,Human_Splice_Rec_1390383,Human_Splice_Rec_1390405,Human_Splice_Rec_1390429,Human_Splice_Rec_1390438,Human_Splice_Rec_1390439,Human_Splice_Rec_1390451,Human_Splice_Rec_1390461,Human_Splice_Rec_1390467,Human_Splice_Rec_1390479,Human_Splice_Rec_1390485 Clinvar_Rec_519 RMVar_hsa_circ_122469,RMVar_hsa_circ_113095,RMVar_hsa_circ_157746,RMVar_hsa_circ_157745 91089 RMVar_ID_91089 Human_SNP_ID_502757407 m1A Human chr12 - 57751668 57751668 57751668 TGAGCCAGTGGCTGAAATTGGTGTCGGTGCCTATGGGACAGTGTACAAGGCCCGTGATCCCCACA TGAGCCAGTGGCTGAAATTGGTGTCGGTGCCTGTGGGACAGTGTACAAGGCCCGTGATCCCCACA T C CDK4 Ensembl:ENSG00000135446 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57751617..57751767 32194978 MeRIP-seq:(Medium) rs781527596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425040,Human_RBP_ID_1475277,Human_RBP_ID_1798353,Human_RBP_ID_4235363,Human_RBP_ID_5417205,Human_RBP_ID_5437905,Human_RBP_ID_5491851,Human_RBP_ID_6203988,Human_RBP_ID_8380820,Human_RBP_ID_8784018,Human_RBP_ID_9278346,Human_RBP_ID_9322593,Human_RBP_ID_11996585,Human_RBP_ID_17650793,Human_RBP_ID_17823835,Human_RBP_ID_18630695,Human_RBP_ID_23568358,Human_RBP_ID_26909922 Human_Splice_Rec_1390368,Human_Splice_Rec_1390382,Human_Splice_Rec_1390404,Human_Splice_Rec_1390428,Human_Splice_Rec_1390450,Human_Splice_Rec_1390460,Human_Splice_Rec_1390474,Human_Splice_Rec_1390478,Human_Splice_Rec_1390484,Human_Splice_Rec_1390488 RMVar_hsa_circ_122469,RMVar_hsa_circ_113095,RMVar_hsa_circ_157746,RMVar_hsa_circ_157745 91090 RMVar_ID_91090 Human_SNP_ID_502757595 m1A Human chr12 - 57752323 57752322 57752323 TGGCAGCTGGTCACATGGTGAGGGTGGGGGTGAGGGGGCCTCTCTAGCTTGCGGCCTGTGTCTAT TGGCAGCTGGTCACATGGTGAGGGTGGGGGTG_GGGGGCCTCTCTAGCTTGCGGCCTGTGTCTAT CT C CDK4 Ensembl:ENSG00000135446 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:57752233..57752322 26863410 MeRIP-seq:(Medium) rs751323591 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_425050,Human_RBP_ID_17823837 RMVar_hsa_circ_113095,RMVar_hsa_circ_157745 91091 RMVar_ID_91091 Human_SNP_ID_502758325 m1A Human chr12 - 57755149 57755149 57755149 TCTCTCGGTCCCAGTCCCCCTCCGGCTCCGGGATCAGGCTTGGCTCGGCCCGTGCGCTCGGCGGT TCTCTCGGTCCCAGTCCCCCTCCGGCTCCGGGGTCAGGCTTGGCTCGGCCCGTGCGCTCGGCGGT T C CDK4 Ensembl:ENSG00000135446 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57755103..57755285 26863196 MeRIP-seq:(Medium) rs1164398967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5171770,Human_RBP_ID_26755580 91092 RMVar_ID_91092 Human_SNP_ID_502758404 m1A Human chr12 - 57755425 57755420 57755425 AGGCCGGGAAGGGGGCGCGCGCTAGAGAGCCGAGCCGGGCCGGGGTCTTCGGGGCCTGCGACAGC AGGCCGGGAAGGGGGCGCGCGCTAGAGAGCCG_____GGCCGGGGTCTTCGGGGCCTGCGACAGC CCGGCT C CDK4 Ensembl:ENSG00000135446 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:57755325..57755426 26863410 MeRIP-seq:(Medium) rs1042677463 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3418976,Human_RBP_ID_8230056,Human_RBP_ID_9415889,Human_RBP_ID_18457058,Human_RBP_ID_26777398 91093 RMVar_ID_91093 Human_SNP_ID_502758421 m1A Human chr12 - 57755463 57755456 57755463 AGGGGGGCTCGCTAGCGGCGGGGGGAGGGGAGAGGACAAGGCCGGGAAGGGGGCGCGCGCTAGAG AGGGGGGCTCGCTAGCGGCGGGGGGAGGGGAG_______GGCCGGGAAGGGGGCGCGCGCTAGAG CTTGTCCT C CDK4 Ensembl:ENSG00000135446 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57755344..57755463 26863196 MeRIP-seq:(Medium) rs1315953761 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_3418976,Human_RBP_ID_8230056,Human_RBP_ID_9415889,Human_RBP_ID_18457058 91094 RMVar_ID_91094 Human_SNP_ID_502758545 m1A Human chr12 - 57755667 57755667 57755667 CTCCTCCTCGTCGCCGTCGCCGTCCCGGGTGGAGCAGCCAGCGAAGGGCGCCCAGCCGCAGCCGC CTCCTCCTCGTCGCCGTCGCCGTCCCGGGTGGGGCAGCCAGCGAAGGGCGCCCAGCCGCAGCCGC T C CDK4 Ensembl:ENSG00000135446 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57755533..57755788 26863196 MeRIP-seq:(Medium) rs1304010246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26755582 91095 RMVar_ID_91095 Human_SNP_ID_502758568 m1A Human chr12 - 57755703 57755703 57755703 GGCCAGGCCCCGGGCCCGCGGCTCCGACCCGTAGTACTCCTCCTCGTCGCCGTCGCCGTCCCGGG GGCCAGGCCCCGGGCCCGCGGCTCCGACCCGTTGTACTCCTCCTCGTCGCCGTCGCCGTCCCGGG T A CDK4 Ensembl:ENSG00000135446 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:57755602..57755797 26863410 MeRIP-seq:(Medium) rs1164068315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26755583 91096 RMVar_ID_91096 Human_SNP_ID_502763233 m1A Human chr12 - 57771960 57771960 57771960 CGGACCACACGCTGCGCTAGTGAGGAGTGGGCAGAGGGAGAGAGAGGAGGGCGGGATTCTCAAAG CGGACCACACGCTGCGCTAGTGAGGAGTGGGCGGAGGGAGAGAGAGGAGGGCGGGATTCTCAAAG T C METTL1 Ensembl:ENSG00000037897 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:57771926..57772039 26863196 MeRIP-seq:(Medium) rs556221752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19058584 91097 RMVar_ID_91097 Human_SNP_ID_502763234 m1A Human chr12 - 57771960 57771960 57771960 CGGACCACACGCTGCGCTAGTGAGGAGTGGGCAGAGGGAGAGAGAGGAGGGCGGGATTCTCAAAG CGGACCACACGCTGCGCTAGTGAGGAGTGGGCCGAGGGAGAGAGAGGAGGGCGGGATTCTCAAAG T G METTL1 Ensembl:ENSG00000037897 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:57771926..57772039 26863196 MeRIP-seq:(Medium) rs556221752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19058584 91098 RMVar_ID_91098 Human_SNP_ID_502763277 m1A Human chr12 - 57772054 57772054 57772054 ATCATGGCAGCCGAGACTCGGAACGTGGCCGGAGCAGAGGCCCCACCGCCCCAGAAGCGCTACTA ATCATGGCAGCCGAGACTCGGAACGTGGCCGGGGCAGAGGCCCCACCGCCCCAGAAGCGCTACTA T C METTL1 Ensembl:ENSG00000037897 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:57771201..57772100;chr12:57771485..57772100;chr12:57771926..57772080 26863196 MeRIP-seq:(Medium) rs1024737943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755377 Human_Splice_Rec_1390553,Human_Splice_Rec_1390563,Human_Splice_Rec_1390581,Human_Splice_Rec_1390587,Human_Splice_Rec_1390595,Human_Splice_Rec_1390599 91099 RMVar_ID_91099 Human_SNP_ID_502766043 m1A Human chr12 - 57782817 57782817 57782817 CCCGGTCCGCGCGACCAGAAACACGCGCAGCGACCGCAGCAGCGACATCTCTCTAGCCGCGATAA CCCGGTCCGCGCGACCAGAAACACGCGCAGCGCCCGCAGCAGCGACATCTCTCTAGCCGCGATAA T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57782751..57783190 26863196 MeRIP-seq:(Medium) rs1313764950 Functional Loss SNV dbSNP153 33..33 33 - - - 91100 RMVar_ID_91100 Human_SNP_ID_502766054 m1A Human chr12 - 57782827 57782827 57782827 CCGGGTAGCTCCCGGTCCGCGCGACCAGAAACACGCGCAGCGACCGCAGCAGCGACATCTCTCTA CCGGGTAGCTCCCGGTCCGCGCGACCAGAAACTCGCGCAGCGACCGCAGCAGCGACATCTCTCTA T A RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57782776..57782915 26863196 MeRIP-seq:(Medium) rs1412270363 Functional Loss SNV dbSNP153 33..33 33 - - - 91101 RMVar_ID_91101 Human_SNP_ID_502766206 m1A Human chr12 - 57783160 57783160 57783160 TTGCTGGAGGCCGAGGCAGACAGACGGGGCCCAGCATAAAATGTGTGCCTTGGCTGGGGCGACTG TTGCTGGAGGCCGAGGCAGACAGACGGGGCCCGGCATAAAATGTGTGCCTTGGCTGGGGCGACTG T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57783088..57783200 26863196 MeRIP-seq:(Medium) rs530450005 Functional Loss SNV dbSNP153 33..33 33 - - - 91102 RMVar_ID_91102 Human_SNP_ID_502776606 m1A Human chr12 - 57821427 57821427 57821427 TTCCGCCCTCCCTTGGATCTCCATGTTTTTCCAGATGGCGGAAGAGCATGTGCCACCCCCTTTCC TTCCGCCCTCCCTTGGATCTCCATGTTTTTCCTGATGGCGGAAGAGCATGTGCCACCCCCTTTCC T A CTDSP2 Ensembl:ENSG00000175215 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57821376..57821450 32194978 MeRIP-seq:(Medium) rs1485299329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178079,Human_RBP_ID_11997773,Human_RBP_ID_17357263,Human_RBP_ID_18935523,Human_RBP_ID_26422489 Human_miRNA_ID_1546032 RMVar_hsa_circ_91732,RMVar_hsa_circ_108857,RMVar_hsa_circ_157760,RMVar_hsa_circ_157761 91103 RMVar_ID_91103 Human_SNP_ID_502783236 m1A Human chr12 + 57846474 57846463 57846475 ATCCCGCGGGCCCGGGCTGGCTGGGCGGGAGGACGGGCGGGCGCGCGGGCTGGGCTGGGCTGGGG ATCCCGCGGGCCCGGGCTGGCT____________GGGCGGGCGCGCGGGCTGGGCTGGGCTGGGG TGGGCGGGAGGAC T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:57846435..57846675 26863196 MeRIP-seq:(Medium) rs1489942302 Functional Loss DEL dbSNP153 23..34 33 - - - 91104 RMVar_ID_91104 Human_SNP_ID_502783242 m1A Human chr12 + 57846474 57846471 57846475 ATCCCGCGGGCCCGGGCTGGCTGGGCGGGAGGACGGGCGGGCGCGCGGGCTGGGCTGGGCTGGGG ATCCCGCGGGCCCGGGCTGGCTGGGCGGGA____GGGCGGGCGCGCGGGCTGGGCTGGGCTGGGG AGGAC A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:57846435..57846675 26863196 MeRIP-seq:(Medium) rs1022576779 Functional Loss DEL dbSNP153 31..34 33 - - - 91105 RMVar_ID_91105 Human_SNP_ID_502783299 m1A Human chr12 - 57846573 57846573 57846573 GCCGCCTCCCTTCCCGGTCCGGGGAGGAAACGAGAGGGGGGATGTGAACAGCTGTGGAAGTCGGA GCCGCCTCCCTTCCCGGTCCGGGGAGGAAACGGGAGGGGGGATGTGAACAGCTGTGGAAGTCGGA T C CTDSP2 Ensembl:ENSG00000175215 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57846438..57846700 26863196 MeRIP-seq:(Medium) rs1366441445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246182,Human_RBP_ID_5139665,Human_RBP_ID_5314994,Human_RBP_ID_9323155,Human_RBP_ID_21884655,Human_RBP_ID_22437294 RMVar_hsa_circ_108857,RMVar_hsa_circ_157761 91106 RMVar_ID_91106 Human_SNP_ID_502783411 m1A Human chr12 - 57846801 57846801 57846801 AGAGCCGGGAGGCGCGCGGGGGTGGGCGCTGCAGCCGCGGGTTGTTTATCTGGAGTACGGAGGGG AGAGCCGGGAGGCGCGCGGGGGTGGGCGCTGCCGCCGCGGGTTGTTTATCTGGAGTACGGAGGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:57846756..57846916 26863196 MeRIP-seq:(Medium) rs925411398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108857,RMVar_hsa_circ_157761 91107 RMVar_ID_91107 Human_SNP_ID_502804963 m1A Human chr12 + 57941718 57941718 57941718 GAGGTCTGCGGGAGGCATGGCGGGAGCTCCGGACGAGCGCCGGCGGGGCCCCGCGGCAGGGGAGC GAGGTCTGCGGGAGGCATGGCGGGAGCTCCGGTCGAGCGCCGGCGGGGCCCCGCGGCAGGGGAGC A T ATP23 Ensembl:ENSG00000166896 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:57941671..57941786 26863196 MeRIP-seq:(Medium) rs1383010989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246819 91108 RMVar_ID_91108 Human_SNP_ID_503035183 m1A Human chr12 + 58920260 58920260 58920260 GCGCTCATCGCGGTCCAGCGGCCTAGGTCTCTACCCGAAGCTCCCAGCCGGCGCGCGCTCGGGGC GCGCTCATCGCGGTCCAGCGGCCTAGGTCTCTGCCCGAAGCTCCCAGCCGGCGCGCGCTCGGGGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:58920163..58920360 26863196 MeRIP-seq:(Medium) rs1193951941 Functional Loss SNV dbSNP153 33..33 33 - - - 91109 RMVar_ID_91109 Human_SNP_ID_503035187 m1A Human chr12 + 58920273 58920273 58920273 TCCAGCGGCCTAGGTCTCTACCCGAAGCTCCCAGCCGGCGCGCGCTCGGGGCCCGGCACAAACTT TCCAGCGGCCTAGGTCTCTACCCGAAGCTCCCCGCCGGCGCGCGCTCGGGGCCCGGCACAAACTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:58920225..58920507 26863196 MeRIP-seq:(Medium) rs1247976566 Functional Loss SNV dbSNP153 33..33 33 - - - 91110 RMVar_ID_91110 Human_SNP_ID_503035231 m1A Human chr12 - 58920368 58920368 58920368 GGCTTCGCCGCCGGGAGTAAAAGAAGGAATTGACCGGGCAGCGCGAGGGAGGAGCGCGCACGCGA GGCTTCGCCGCCGGGAGTAAAAGAAGGAATTGCCCGGGCAGCGCGAGGGAGGAGCGCGCACGCGA T G LRIG3 Ensembl:ENSG00000139263 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:58920299..58920493 26863196 MeRIP-seq:(Medium) rs1180605222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246186,Human_RBP_ID_6204639,Human_RBP_ID_17824032,Human_RBP_ID_18434577 91111 RMVar_ID_91111 Human_SNP_ID_85629309 m1A Human chr2 + 105099744 105099744 105099744 AGCCAGGCCAAGAGGGAGCCCGCAGAAAGTTTACGTGGAAGAAACGCTAAGGGTTTGCTCCCAGG AGCCAGGCCAAGAGGGAGCCCGCAGAAAGTTTGCGTGGAAGAAACGCTAAGGGTTTGCTCCCAGG A G MRPS9 Ensembl:ENSG00000135972 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:105099620..105099850 26863196 MeRIP-seq:(Medium) rs1167868222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6810492,Human_RBP_ID_9091998,Human_RBP_ID_17658583,Human_RBP_ID_17964132,Human_RBP_ID_23816430 Human_Splice_Rec_283842,Human_Splice_Rec_283858 RMVar_hsa_circ_202294,RMVar_hsa_circ_92836 91112 RMVar_ID_91112 Human_SNP_ID_85682105 m1A Human chr2 - 105308295 105308295 105308295 CTCTTCCAGCAGATCAGCCAGTAGACATGATGAGCATCAAAGCCTTTACGCTTGTCTCTGCTGTG CTCTTCCAGCAGATCAGCCAGTAGACATGATGCGCATCAAAGCCTTTACGCTTGTCTCTGCTGTG T G TGFBRAP1 Ensembl:ENSG00000135966 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:105308247..105308331 26863196 MeRIP-seq:(Medium) rs1351381009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25578177 Human_Splice_Rec_283920 RMVar_hsa_circ_202302,RMVar_hsa_circ_323633,RMVar_hsa_circ_355931 91113 RMVar_ID_91113 Human_SNP_ID_85687291 m1A Human chr2 - 105329663 105329663 105329663 AGCCGCGGGCCGGAGCGGGGCGGCGGGGCCCCAGGCCGCGGGGCGGCGCGGGACGGCGGGCGCCG AGCCGCGGGCCGGAGCGGGGCGGCGGGGCCCCGGGCCGCGGGGCGGCGCGGGACGGCGGGCGCCG T C TGFBRAP1 Ensembl:ENSG00000135966 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:105308234..105329699;chr2:105308123..105329725;chr2:105329583..105329689 26863196 MeRIP-seq:(Medium) rs1190786949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4576803,Human_RBP_ID_18422305 Human_Splice_Rec_283919 91114 RMVar_ID_91114 Human_SNP_ID_85689078 m1A Human chr2 - 105336604 105336604 105336604 ATATTTTGCACATTTAAAACTTAAACTTGGGTATGGTGGCTTATGCCTGTAATCACGGCGTTTTG ATATTTTGCACATTTAAAACTTAAACTTGGGTGTGGTGGCTTATGCCTGTAATCACGGCGTTTTG T C AC012360.3 Ensembl:ENSG00000272994 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2679861 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11815,GWAS_ID_11816,GWAS_ID_11817,GWAS_ID_11818,GWAS_ID_11819,GWAS_ID_11820 91115 RMVar_ID_91115 Human_SNP_ID_85695134 m1A Human chr2 - 105361302 105361302 105361302 CCTCACAGAGAGGGACGACATCCTGTGCCCCGACTGTGGGAAAGACATCTGAATTCAACACAGAG CCTCACAGAGAGGGACGACATCCTGTGCCCCGGCTGTGGGAAAGACATCTGAATTCAACACAGAG T C FHL2 Ensembl:ENSG00000115641 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:105361251..105361400 32194978 MeRIP-seq:(Medium) rs779103780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142906 RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305 91116 RMVar_ID_91116 Human_SNP_ID_85695586 m1A Human chr2 + 105363344 105363344 105363344 ACTTCTTGGCATACAAGTCACAGAAGCAGTTCAGGCAGTAGGCAAAGTCATCGCGAGCTGTGAAG ACTTCTTGGCATACAAGTCACAGAAGCAGTTCGGGCAGTAGGCAAAGTCATCGCGAGCTGTGAAG A G AC108058.1 Ensembl:ENSG00000238273 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:105363276..105363350 32194978 MeRIP-seq:(Medium) rs1285257759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5593850,Human_RBP_ID_8258262 91117 RMVar_ID_91117 Human_SNP_ID_85695625 m1A Human chr2 - 105363450 105363450 105363450 CGTCCCTGCAGCCCATCACCACGGGAGGGGTCACTTACCGGGAGCAGCCCTGGCACAAGGAGTGC CGTCCCTGCAGCCCATCACCACGGGAGGGGTCCCTTACCGGGAGCAGCCCTGGCACAAGGAGTGC T G FHL2 Ensembl:ENSG00000115641 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:105363401..105363450 32194978 MeRIP-seq:(Medium) rs200116659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24485685,Human_RBP_ID_26818838 Human_Splice_Rec_283986,Human_Splice_Rec_283998,Human_Splice_Rec_284010,Human_Splice_Rec_284020,Human_Splice_Rec_284034,Human_Splice_Rec_284044,Human_Splice_Rec_284054,Human_Splice_Rec_284064,Human_Splice_Rec_284074,Human_Splice_Rec_284086 Clinvar_Rec_520 RMVar_hsa_circ_38049,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305,RMVar_hsa_circ_371869,RMVar_hsa_circ_202307 91118 RMVar_ID_91118 Human_SNP_ID_85699590 m1A Human chr2 - 105379628 105379628 105379628 GGGCTGACGTGCCAGGTAAAAAACAGGAGCACAGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG GGGCTGACGTGCCAGGTAAAAAACAGGAGCACTGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG T A FHL2 Ensembl:ENSG00000115641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:105379626..105379773 26863196 MeRIP-seq:(Medium) rs10189100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202310,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305,RMVar_hsa_circ_202308,RMVar_hsa_circ_307296,RMVar_hsa_circ_86098,RMVar_hsa_circ_202311,RMVar_hsa_circ_307374 91119 RMVar_ID_91119 Human_SNP_ID_85699591 m1A Human chr2 - 105379628 105379628 105379628 GGGCTGACGTGCCAGGTAAAAAACAGGAGCACAGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG GGGCTGACGTGCCAGGTAAAAAACAGGAGCACCGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG T G FHL2 Ensembl:ENSG00000115641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:105379626..105379773 26863196 MeRIP-seq:(Medium) rs10189100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202310,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305,RMVar_hsa_circ_202308,RMVar_hsa_circ_307296,RMVar_hsa_circ_86098,RMVar_hsa_circ_202311,RMVar_hsa_circ_307374 91120 RMVar_ID_91120 Human_SNP_ID_85701185 m1A Human chr2 - 105386465 105386462 105386465 GCCACCATTGCAACGAATCTCTCTTTGGCAAGAAGTACATCCTGCGGGAGGAGAGCCCCTACTGC GCCACCATTGCAACGAATCTCTCTTTGGCAAG___TACATCCTGCGGGAGGAGAGCCCCTACTGC ACTT A FHL2 Ensembl:ENSG00000115641 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:105386415..105386570 26863196 MeRIP-seq:(Medium) rs1558703583 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_531471,Human_RBP_ID_1576577,Human_RBP_ID_4623544,Human_RBP_ID_9387220 Human_Splice_Rec_283980,Human_Splice_Rec_283992,Human_Splice_Rec_284004,Human_Splice_Rec_284014,Human_Splice_Rec_284028,Human_Splice_Rec_284038,Human_Splice_Rec_284050,Human_Splice_Rec_284058,Human_Splice_Rec_284068,Human_Splice_Rec_284078,Human_Splice_Rec_284088,Human_Splice_Rec_284092 RMVar_hsa_circ_202310,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305,RMVar_hsa_circ_202308,RMVar_hsa_circ_307296,RMVar_hsa_circ_86098,RMVar_hsa_circ_202311,RMVar_hsa_circ_307374 91121 RMVar_ID_91121 Human_SNP_ID_85701201 m1A Human chr2 + 105386511 105386511 105386511 GATTCGTTGCAATGGTGGCAGTCAAAGCGCTCAGTCATTTTGACTCCTGGCTTTTCAGCAACCTA GATTCGTTGCAATGGTGGCAGTCAAAGCGCTCCGTCATTTTGACTCCTGGCTTTTCAGCAACCTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:105386419..105386572 26863196 MeRIP-seq:(Medium) rs1340694263 Functional Loss SNV dbSNP153 33..33 33 - - - 91122 RMVar_ID_91122 Human_SNP_ID_85793921 m1A Human chr2 + 105745084 105745084 105745084 AAGAGCGGCGCCTGGGCGGGCGCAGCGCGGCCACCGCCCCGGGACCCGCGCCGCTGCCCTCCGGC AAGAGCGGCGCCTGGGCGGGCGCAGCGCGGCCGCCGCCCCGGGACCCGCGCCGCTGCCCTCCGGC A G NCK2 Ensembl:ENSG00000071051 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:105744849..105745184 26863196 MeRIP-seq:(Medium) rs1293487491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777856,Human_RBP_ID_4622609 Human_Splice_Rec_284107,Human_Splice_Rec_284115 91123 RMVar_ID_91123 Human_SNP_ID_85902573 m1A Human chr2 - 106179287 106179287 106179287 GGGCCTTTGTGGAGAGGGTCAGGGGAAGAGCCAGGGTTTGAAGTCAGAGCAAGAGCGGGGGTTCA GGGCCTTTGTGGAGAGGGTCAGGGGAAGAGCCGGGGTTTGAAGTCAGAGCAAGAGCGGGGGTTCA T C UXS1 Ensembl:ENSG00000115652 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:106179284..106179439 26863196 MeRIP-seq:(Medium) rs1194927180 Functional Loss SNV dbSNP153 33..33 33 - - - 91124 RMVar_ID_91124 Human_SNP_ID_85906668 m1A Human chr2 + 106194237 106194237 106194237 CGGCAGACACGAGGCGCAGCAGCGCCTTGCTCACCATCCCCGGGAGCCGCGCGGGTCCAGGGCCC CGGCAGACACGAGGCGCAGCAGCGCCTTGCTCGCCATCCCCGGGAGCCGCGCGGGTCCAGGGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:106194187..106194263 26863196 MeRIP-seq:(Medium) rs902701008 Functional Loss SNV dbSNP153 33..33 33 - - - 91125 RMVar_ID_91125 Human_SNP_ID_86059645 m1A Human chr2 - 106772448 106772448 106772448 CCTCTGAAGAACACGGATGATTTCATATAAGAAACCTGGCAATCAAGGACATCAGGGACCTGAAA CCTCTGAAGAACACGGATGATTTCATATAAGACACCTGGCAATCAAGGACATCAGGGACCTGAAA T G lnc-ST6GAL2-6 RNACentral:URS00008B57BA lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:106772360..106772487 26863196 MeRIP-seq:(Medium) rs1045385679 Functional Loss SNV dbSNP153 33..33 33 - - - 91126 RMVar_ID_91126 Human_SNP_ID_86061420 m1A Human chr2 + 106779966 106779966 106779966 TTTAAGTACCCTGGAAGTCACCTCAGCGAGAGAGGGGCTAGCAATAATGAGGGTGGGGCAATAGC TTTAAGTACCCTGGAAGTCACCTCAGCGAGAGCGGGGCTAGCAATAATGAGGGTGGGGCAATAGC A C lnc-CD8B2-5,lnc-CD8B2-5:2 RNACentral:URS00008BD6ED,RNACentral:URS00008B307D lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:106779926..106780039 26863196 MeRIP-seq:(Medium) rs892802511 Functional Loss SNV dbSNP153 33..33 33 - - - 91127 RMVar_ID_91127 Human_SNP_ID_86480848 m1A Human chr2 - 108449267 108449256 108449267 TGGGCCCGACCTGAGTTACCTCCATCTCCGCCAGCCCGCCGCCGGCCCGCAACCAGCCGCCGCCA TGGGCCCGACCTGAGTTACCTCCATCTCCGCC___________GGCCCGCAACCAGCCGCCGCCA CGGCGGCGGGCT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:108449218..108449363 26863196 MeRIP-seq:(Medium) rs776397797 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_202362,RMVar_hsa_circ_115464 91128 RMVar_ID_91128 Human_SNP_ID_86480870 m1A Human chr2 - 108449282 108449282 108449282 CTTGATGGGAGGCAGTGGGCCCGACCTGAGTTACCTCCATCTCCGCCAGCCCGCCGCCGGCCCGC CTTGATGGGAGGCAGTGGGCCCGACCTGAGTTCCCTCCATCTCCGCCAGCCCGCCGCCGGCCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:108449246..108449329;chr2:108449246..108449332;chr2:108449240..108449352;chr2:108449239..108449324 26863196 MeRIP-seq:(Medium) rs565602080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202362,RMVar_hsa_circ_115464 91129 RMVar_ID_91129 Human_SNP_ID_86481058 m1A Human chr2 - 108449671 108449671 108449671 AGTATTCTCTTCACCTTAGATTTCCCGGTCCCAGGGGTAGCTGGTGAAGCCACCCCATCTTGAAC AGTATTCTCTTCACCTTAGATTTCCCGGTCCCCGGGGTAGCTGGTGAAGCCACCCCATCTTGAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:108449634..108449745 26863196 MeRIP-seq:(Medium) rs777363501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202362,RMVar_hsa_circ_115464 91130 RMVar_ID_91130 Human_SNP_ID_86481515 m1A Human chr2 + 108450977 108450977 108450977 TTTTCTAGCAGACATTGTTTCTTTTTTGTGGTATACTAGAAACATGAGTTATAACAAGTTGGTAA TTTTCTAGCAGACATTGTTTCTTTTTTGTGGTGTACTAGAAACATGAGTTATAACAAGTTGGTAA A G GCC2 Ensembl:ENSG00000135968 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:108450975..108451040 26863196 MeRIP-seq:(Medium) rs756784480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915744 RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_58349,RMVar_hsa_circ_360937 91131 RMVar_ID_91131 Human_SNP_ID_86504988 m1A Human chr2 - 108534138 108534138 108534138 GGCTGGGGTAGGGGCTCATTGGGAGCCCACGGAGCGCGGCGGCGGCTCGGGGGCCGAGTTCCCTA GGCTGGGGTAGGGGCTCATTGGGAGCCCACGGCGCGCGGCGGCGGCTCGGGGGCCGAGTTCCCTA T G GCC2-AS1 Ensembl:ENSG00000214184 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:108534034..108534148 26863196 MeRIP-seq:(Medium) rs1013909415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421865 91132 RMVar_ID_91132 Human_SNP_ID_86505206 m1A Human chr2 - 108534455 108534455 108534455 CCGCCGCGGCCGGCTACTGGCGGGCCCGGAGCAGGAAGGGGAGGAAGGCCAGGGGCCGGCCGCGC CCGCCGCGGCCGGCTACTGGCGGGCCCGGAGCCGGAAGGGGAGGAAGGCCAGGGGCCGGCCGCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:108534353..108534528 26863410 MeRIP-seq:(Medium) rs912291121 Functional Loss SNV dbSNP153 33..33 33 - - - 91133 RMVar_ID_91133 Human_SNP_ID_86505235 m1A Human chr2 + 108534510 108534510 108534510 GCCGCGGCGGCGAGGGACTAGGACGCGGCTGGAGCGGCGCCGGGAGACGAGGGGCTGAGAGACGG GCCGCGGCGGCGAGGGACTAGGACGCGGCTGGGGCGGCGCCGGGAGACGAGGGGCTGAGAGACGG A G LIMS1 Ensembl:ENSG00000169756 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr2:108534359..108534546;chr2:108534451..108534639 26863410,26863196 MeRIP-seq:(Medium) rs1192562395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776476,Human_RBP_ID_922944,Human_RBP_ID_4623553,Human_RBP_ID_9330623,Human_RBP_ID_22997190 Human_Splice_Rec_285087,Human_Splice_Rec_285105 Human_miRNA_ID_2972402,Human_miRNA_ID_2972403,Human_miRNA_ID_3005586,Human_miRNA_ID_3005587 RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 91134 RMVar_ID_91134 Human_SNP_ID_86505251 m1A Human chr2 + 108534552 108534551 108534552 GGAGACGAGGGGCTGAGAGACGGCGGCGGCCGAAAGCGGAGAGATGCTGGGCGTGGCGGCCGGGA GGAGACGAGGGGCTGAGAGACGGCGGCGGCCG_AAGCGGAGAGATGCTGGGCGTGGCGGCCGGGA GA G LIMS1 Ensembl:ENSG00000169756 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:108534397..108534665 26863196 MeRIP-seq:(Medium) rs1424812986 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4577116,Human_RBP_ID_22997190 Human_Splice_Rec_285087,Human_Splice_Rec_285105 RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 91135 RMVar_ID_91135 Human_SNP_ID_86571536 m1A Human chr2 + 108786846 108786846 108786846 CTGTGTGCTATGGAGCCGAGGGTCGTCAAGCCACCGGGGCAGGATTTAGTAGTGGAGAGTCTCAA CTGTGTGCTATGGAGCCGAGGGTCGTCAAGCCGCCGGGGCAGGATTTAGTAGTGGAGAGTCTCAA A G CCDC138 Ensembl:ENSG00000163006 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:108786796..108786942 26863196 MeRIP-seq:(Medium) rs766473132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8498673,Human_RBP_ID_9384524,Human_RBP_ID_13573669,Human_RBP_ID_18421866,Human_RBP_ID_22242269,Human_RBP_ID_27840073 Human_Splice_Rec_285317,Human_Splice_Rec_285343,Human_Splice_Rec_285369,Human_Splice_Rec_285405 Human_miRNA_ID_2150561,Human_miRNA_ID_2150562,Human_miRNA_ID_2150563,Human_miRNA_ID_2150564,Human_miRNA_ID_2419054,Human_miRNA_ID_2419055,Human_miRNA_ID_2419056,Human_miRNA_ID_2419057 RMVar_hsa_circ_108815,RMVar_hsa_circ_202417 91136 RMVar_ID_91136 Human_SNP_ID_86769553 m1A Human chr2 - 109562295 109562293 109562295 TCCAGGCATGAGAAGATGGAGGCGTGAAAGAGAGGGGTAGTGACAGAGGGGTGAGAAGCATGCTT TCCAGGCATGAGAAGATGGAGGCGTGAAAGAG__GGGTAGTGACAGAGGGGTGAGAAGCATGCTT CCT C SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:109562292..109562449 26863196 MeRIP-seq:(Medium) rs1377537164 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_830448 RMVar_hsa_circ_4144,RMVar_hsa_circ_376335,RMVar_hsa_circ_202456,RMVar_hsa_circ_20334,RMVar_hsa_circ_272325,RMVar_hsa_circ_202455,RMVar_hsa_circ_349478,RMVar_hsa_circ_126012,RMVar_hsa_circ_202457 91137 RMVar_ID_91137 Human_SNP_ID_86769559 m1A Human chr2 - 109562295 109562295 109562295 TCCAGGCATGAGAAGATGGAGGCGTGAAAGAGAGGGGTAGTGACAGAGGGGTGAGAAGCATGCTT TCCAGGCATGAGAAGATGGAGGCGTGAAAGAGCGGGGTAGTGACAGAGGGGTGAGAAGCATGCTT T G SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:109562292..109562449 26863196 MeRIP-seq:(Medium) rs1020925406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830448 RMVar_hsa_circ_4144,RMVar_hsa_circ_376335,RMVar_hsa_circ_202456,RMVar_hsa_circ_20334,RMVar_hsa_circ_272325,RMVar_hsa_circ_202455,RMVar_hsa_circ_349478,RMVar_hsa_circ_126012,RMVar_hsa_circ_202457 91138 RMVar_ID_91138 Human_SNP_ID_86783026 m1A Human chr2 - 109613884 109613884 109613884 TGCCCTCCGGCCTTCCCGCCGCCGTCGCCGGGACCAGCCGCTCGGGGCCGGGCTGATACAGCCGC TGCCCTCCGGCCTTCCCGCCGCCGTCGCCGGGCCCAGCCGCTCGGGGCCGGGCTGATACAGCCGC T G SEPTIN10 Ensembl:ENSG00000186522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:109613762..109613949 26863196 MeRIP-seq:(Medium) rs528250060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624634,Human_RBP_ID_18421867,Human_RBP_ID_22077711 Human_Splice_Rec_285513,Human_Splice_Rec_285531,Human_Splice_Rec_285551,Human_Splice_Rec_285567,Human_Splice_Rec_285589,Human_Splice_Rec_285615,Human_Splice_Rec_285625,Human_Splice_Rec_285633,Human_Splice_Rec_285641,Human_Splice_Rec_285647 RMVar_hsa_circ_90874,RMVar_hsa_circ_202459 91139 RMVar_ID_91139 Human_SNP_ID_86783413 m1A Human chr2 + 109614629 109614629 109614629 GCACTTCAGGGGCGCCCTAGGCGGCGAACCGGAGCAGCGCGCCCGCGCCCGCGCGCACTTCAAGG GCACTTCAGGGGCGCCCTAGGCGGCGAACCGGGGCAGCGCGCCCGCGCCCGCGCGCACTTCAAGG A G SOWAHC Ensembl:ENSG00000198142 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:109614383..109614681 26863196 MeRIP-seq:(Medium) rs1203649796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622616,Human_RBP_ID_22077712 91140 RMVar_ID_91140 Human_SNP_ID_86783545 m1A Human chr2 + 109614876 109614876 109614876 CCCGACGCGGCGGCCCCGGAGTCGCTCCCTGGACAGGGCCGCGAGCTGGGCGAGGGAGAGCCCCC CCCGACGCGGCGGCCCCGGAGTCGCTCCCTGGTCAGGGCCGCGAGCTGGGCGAGGGAGAGCCCCC A T SOWAHC Ensembl:ENSG00000198142 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:109614825..109614941 26863196 MeRIP-seq:(Medium) rs1006862654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8841286 91141 RMVar_ID_91141 Human_SNP_ID_86783690 m1A Human chr2 - 109615126 109615126 109615126 CCCGGGACACACGCTCCTCTTCAGCTGCGGGGAGCTGCCCATCACCAGGTCACGGAGGTTCTGGC CCCGGGACACACGCTCCTCTTCAGCTGCGGGGCGCTGCCCATCACCAGGTCACGGAGGTTCTGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr2:109615076..109615275;chr2:109615076..109615226 26863196,32194978 MeRIP-seq:(Medium) rs1385151974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202471 91142 RMVar_ID_91142 Human_SNP_ID_86783752 m1A Human chr2 + 109615255 109615255 109615255 CATCGGTGGCCTCGTCGTCCGCGGAGGAGGAGAGCAGCGGCGGAGGCTCCGTGACGCTGGACCCC CATCGGTGGCCTCGTCGTCCGCGGAGGAGGAGGGCAGCGGCGGAGGCTCCGTGACGCTGGACCCC A G SOWAHC Ensembl:ENSG00000198142 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:109615126..109615325 26863196 MeRIP-seq:(Medium) rs1246234200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776639,Human_RBP_ID_828853,Human_RBP_ID_5147531 Human_miRNA_ID_2208358,Human_miRNA_ID_2208359,Human_miRNA_ID_2208360,Human_miRNA_ID_3032964,Human_miRNA_ID_3032965,Human_miRNA_ID_3032966 91143 RMVar_ID_91143 Human_SNP_ID_86783950 m1A Human chr2 + 109615682 109615672 109615683 CGAGGAGATCAAGAACCTGGTGGGAGCCCTGGACGAGGGTGACGGGGAAAGCGCCGCGGGTAGCG CGAGGAGATCAAGAACCTGGTGG___________GAGGGTGACGGGGAAAGCGCCGCGGGTAGCG GGAGCCCTGGAC G SOWAHC Ensembl:ENSG00000198142 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:109615632..109615740 26863196 MeRIP-seq:(Medium) rs1321951007 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_776640,Human_RBP_ID_920701,Human_RBP_ID_8841291,Human_RBP_ID_22078201 91144 RMVar_ID_91144 Human_SNP_ID_86820112 m1A Human chr2 - 109794634 109794634 109794634 GCCCCTCGGGAGACATGACGCCTGAGCCATCGAGGCGGCCGCCGCCGCCGCCCCCCCCGCCGCCG GCCCCTCGGGAGACATGACGCCTGAGCCATCGCGGCGGCCGCCGCCGCCGCCCCCCCCGCCGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr2:109794540..109794656;chr2:109794494..109794713;chr2:109794491..109794717;chr2:109794510..109794705 26863196 MeRIP-seq:(Medium) rs1450107607 Functional Loss SNV dbSNP153 33..33 33 - - - 91145 RMVar_ID_91145 Human_SNP_ID_86820445 m1A Human chr2 + 109813631 109813631 109813631 GTTCAATGGCGAGCTCTTTCTGAGCTGGCTGCATTGTGCTATCTCATAGCATTTCAGGTAAGTCT GTTCAATGGCGAGCTCTTTCTGAGCTGGCTGCGTTGTGCTATCTCATAGCATTTCAGGTAAGTCT A G RGPD5 Ensembl:ENSG00000015568 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1553471780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_285679,Human_Splice_Rec_285715,Human_Splice_Rec_285757,Human_Splice_Rec_285807 Human_miRNA_ID_1378643 RMVar_hsa_circ_36378,RMVar_hsa_circ_325624,RMVar_hsa_circ_306726,RMVar_hsa_circ_74728,RMVar_hsa_circ_378088 91146 RMVar_ID_91146 Human_SNP_ID_86824884 m1A Human chr2 + 109989818 109989818 109989818 TATTTGTGAATTTTATAAAGTACAGCTTATCTATATTTTCTATTATACTTGTGGTTTTGGTATGA TATTTGTGAATTTTATAAAGTACAGCTTATCTGTATTTTCTATTATACTTGTGGTTTTGGTATGA A G LINC01123 Ensembl:ENSG00000204588 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62159146 Functional Loss SNV dbSNP153 33..33 33 - - - 91147 RMVar_ID_91147 Human_SNP_ID_86856928 m1A Human chr2 - 110169924 110169924 110169924 AGATAGTGAAGACAGTGGTGGGGAGGAAGAAGATGCAGAGGAGGAAGAGGAAGAGAAAGAGGAAA AGATAGTGAAGACAGTGGTGGGGAGGAAGAAGGTGCAGAGGAGGAAGAGGAAGAGAAAGAGGAAA T C NPHP1 Ensembl:ENSG00000144061 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:110169880..110169972 26863196 MeRIP-seq:(Medium) rs747176517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_286080,Human_Splice_Rec_286118,Human_Splice_Rec_286156,Human_Splice_Rec_286192,Human_Splice_Rec_286222,Human_Splice_Rec_286254,Human_Splice_Rec_286290 RMVar_hsa_circ_753,RMVar_hsa_circ_29139,RMVar_hsa_circ_18599,RMVar_hsa_circ_356985,RMVar_hsa_circ_28573 91148 RMVar_ID_91148 Human_SNP_ID_86866678 m1A Human chr2 - 110212221 110212221 110212221 AGTCCCCGCCTGCCATGGCCGGCTCTTCCTGGAGTGTTGGTGAGCAGTACACATAGTGACATTGC AGTCCCCGCCTGCCATGGCCGGCTCTTCCTGGTGTGTTGGTGAGCAGTACACATAGTGACATTGC T A MTLN Ensembl:ENSG00000175701 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:110212218..110212463 32194978 MeRIP-seq:(Medium) rs1007394468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_531991,Human_RBP_ID_8498957,Human_RBP_ID_17658149,Human_RBP_ID_19101356,Human_RBP_ID_23818000 Human_Splice_Rec_286357,Human_Splice_Rec_286359,Human_Splice_Rec_286363 91149 RMVar_ID_91149 Human_SNP_ID_86866679 m1A Human chr2 - 110212221 110212221 110212221 AGTCCCCGCCTGCCATGGCCGGCTCTTCCTGGAGTGTTGGTGAGCAGTACACATAGTGACATTGC AGTCCCCGCCTGCCATGGCCGGCTCTTCCTGGGGTGTTGGTGAGCAGTACACATAGTGACATTGC T C MTLN Ensembl:ENSG00000175701 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:110212218..110212463 32194978 MeRIP-seq:(Medium) rs1007394468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_531991,Human_RBP_ID_8498957,Human_RBP_ID_17658149,Human_RBP_ID_19101356,Human_RBP_ID_23818000 Human_Splice_Rec_286357,Human_Splice_Rec_286359,Human_Splice_Rec_286363 91150 RMVar_ID_91150 Human_SNP_ID_86866740 m1A Human chr2 - 110212405 110212405 110212405 TGCGGAGGCGCTACTTGGACTGGAGGAAAAGGAGGCTGCAGGACAAGCTGGCGGCGACGCAGAAG TGCGGAGGCGCTACTTGGACTGGAGGAAAAGGGGGCTGCAGGACAAGCTGGCGGCGACGCAGAAG T C MTLN Ensembl:ENSG00000175701 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:110212376..110212521 26863196 MeRIP-seq:(Medium) rs1316409587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3592025,Human_RBP_ID_4623556,Human_RBP_ID_5118342,Human_RBP_ID_5422152,Human_RBP_ID_17658151 91151 RMVar_ID_91151 Human_SNP_ID_86866763 m1A Human chr2 - 110212497 110212497 110212497 AGCCATGGCGGATGTGTCAGAGAGGACACTGCAGTTGTCCGTGCTAGTAGCCTTCGCTTCTGGAG AGCCATGGCGGATGTGTCAGAGAGGACACTGCCGTTGTCCGTGCTAGTAGCCTTCGCTTCTGGAG T G MTLN Ensembl:ENSG00000175701 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:110212384..110212525 26863196 MeRIP-seq:(Medium) rs1351616934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1576780,Human_RBP_ID_4577718,Human_RBP_ID_5118342,Human_RBP_ID_5471431,Human_RBP_ID_8942700 Human_Splice_Rec_286362 91152 RMVar_ID_91152 Human_SNP_ID_86905381 m1A Human chr2 + 110610825 110610825 110610825 GCCGCTGCCGCCGCTGCCGCCGCCGCCGCCGAAGCTCGGGCCGCCCGCGCGCTGCGACGAAAGGC GCCGCTGCCGCCGCTGCCGCCGCCGCCGCCGAGGCTCGGGCCGCCCGCGCGCTGCGACGAAAGGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:110610770..110610857 26863410 MeRIP-seq:(Medium) rs1281643458 Functional Loss SNV dbSNP153 33..33 33 - - - 91153 RMVar_ID_91153 Human_SNP_ID_86911076 m1A Human chr2 - 110642197 110642197 110642197 AAGCTGGTCTATGTCCATCACCTTCTTGGAGAAGGAGCCTTTGCCCAGGTGTACGAAGCTACCCA AAGCTGGTCTATGTCCATCACCTTCTTGGAGACGGAGCCTTTGCCCAGGTGTACGAAGCTACCCA T G BUB1 Ensembl:ENSG00000169679 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:110642149..110642463 32194978 MeRIP-seq:(Medium) rs746371172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_532011,Human_RBP_ID_915746,Human_RBP_ID_1895634,Human_RBP_ID_4577751,Human_RBP_ID_8851498,Human_RBP_ID_9259887,Human_RBP_ID_9296783,Human_RBP_ID_22452417 Human_Splice_Rec_286786,Human_Splice_Rec_286787,Human_Splice_Rec_286828,Human_Splice_Rec_286829,Human_Splice_Rec_286848,Human_Splice_Rec_286849,Human_Splice_Rec_286892,Human_Splice_Rec_286893,Human_Splice_Rec_286902,Human_Splice_Rec_286903,Human_Splice_Rec_286946 Human_miRNA_ID_2788010,Human_miRNA_ID_2788011,Human_miRNA_ID_2788012,Human_miRNA_ID_2788013,Human_miRNA_ID_2817624,Human_miRNA_ID_2817625,Human_miRNA_ID_2817626,Human_miRNA_ID_2817627 RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500,RMVar_hsa_circ_125481,RMVar_hsa_circ_120849,RMVar_hsa_circ_110025,RMVar_hsa_circ_114948,RMVar_hsa_circ_105431,RMVar_hsa_circ_202503,RMVar_hsa_circ_202507,RMVar_hsa_circ_89069,RMVar_hsa_circ_89718,RMVar_hsa_circ_202509,RMVar_hsa_circ_82746,RMVar_hsa_circ_202508,RMVar_hsa_circ_202505,RMVar_hsa_circ_202506,RMVar_hsa_circ_202504,RMVar_hsa_circ_28105,RMVar_hsa_circ_104794,RMVar_hsa_circ_202502,RMVar_hsa_circ_120145,RMVar_hsa_circ_202512,RMVar_hsa_circ_202513 91154 RMVar_ID_91154 Human_SNP_ID_86912926 m1A Human chr2 - 110650687 110650687 110650687 GTCTGAGCCAGCCTGCTGCAGGTGGGGTACTTACCTGTGAGGCAGAGTTGGGCGTTGAGGCTTGC GTCTGAGCCAGCCTGCTGCAGGTGGGGTACTTGCCTGTGAGGCAGAGTTGGGCGTTGAGGCTTGC T C BUB1 Ensembl:ENSG00000169679 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:110649236..110650754 32194978 MeRIP-seq:(Medium) rs1291332055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4577756,Human_RBP_ID_6813536,Human_RBP_ID_8841317,Human_RBP_ID_9296784,Human_RBP_ID_9387254,Human_RBP_ID_22450521 Human_Splice_Rec_286782,Human_Splice_Rec_286824,Human_Splice_Rec_286844,Human_Splice_Rec_286888,Human_Splice_Rec_286942 Human_miRNA_ID_2776501,Human_miRNA_ID_2776502,Human_miRNA_ID_2776503,Human_miRNA_ID_2776504 RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500,RMVar_hsa_circ_125481,RMVar_hsa_circ_110025,RMVar_hsa_circ_114948,RMVar_hsa_circ_105431,RMVar_hsa_circ_202503,RMVar_hsa_circ_202507,RMVar_hsa_circ_89069,RMVar_hsa_circ_89718,RMVar_hsa_circ_82746,RMVar_hsa_circ_202508,RMVar_hsa_circ_202505,RMVar_hsa_circ_202506,RMVar_hsa_circ_202504,RMVar_hsa_circ_28105,RMVar_hsa_circ_202502,RMVar_hsa_circ_120145,RMVar_hsa_circ_202513,RMVar_hsa_circ_202515,RMVar_hsa_circ_104411,RMVar_hsa_circ_124716,RMVar_hsa_circ_277870,RMVar_hsa_circ_19949,RMVar_hsa_circ_202516,RMVar_hsa_circ_90065,RMVar_hsa_circ_202514,RMVar_hsa_circ_202517 91155 RMVar_ID_91155 Human_SNP_ID_86914409 m1A Human chr2 + 110657574 110657574 110657574 TTACCCATAATTTTCTTTGTTTCCATCTTCAAACACATGAAAAGCAGATGACAAAGAAGAGATGA TTACCCATAATTTTCTTTGTTTCCATCTTCAATCACATGAAAAGCAGATGACAAAGAAGAGATGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:110653503..110657615 32194978 MeRIP-seq:(Medium) rs1288396578 Functional Loss SNV dbSNP153 33..33 33 - - - 91156 RMVar_ID_91156 Human_SNP_ID_86918048 m1A Human chr2 + 110672721 110672721 110672721 GTTCAGCCTGGTTTTGAATTCCTCTCTGAAGGACAGCACTGGCATGCTGCAGCTCTCCTTGGGCT GTTCAGCCTGGTTTTGAATTCCTCTCTGAAGGGCAGCACTGGCATGCTGCAGCTCTCCTTGGGCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:110669552..110672825 32194978 MeRIP-seq:(Medium) rs750544206 Functional Loss SNV dbSNP153 33..33 33 - - - 91157 RMVar_ID_91157 Human_SNP_ID_86919487 m1A Human chr2 - 110678009 110678009 110678009 AGTTTGCGGTTCAGGTTTGGCCGCTGCCGGCCAGCGTCCTCTGGCCATGGACACCCCGGAAAATG AGTTTGCGGTTCAGGTTTGGCCGCTGCCGGCCGGCGTCCTCTGGCCATGGACACCCCGGAAAATG T C BUB1 Ensembl:ENSG00000169679 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:110677930..110678015;chr2:110677925..110678011 26863196 MeRIP-seq:(Medium) rs997101376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_532032,Human_RBP_ID_4623559,Human_RBP_ID_5471433,Human_RBP_ID_8852087,Human_RBP_ID_9330626,Human_RBP_ID_18421868 Human_Splice_Rec_286751,Human_Splice_Rec_286795,Human_Splice_Rec_286857,Human_Splice_Rec_286911,Human_Splice_Rec_286969,Human_Splice_Rec_286993,Human_Splice_Rec_287003 RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500,RMVar_hsa_circ_114948,RMVar_hsa_circ_202502 91158 RMVar_ID_91158 Human_SNP_ID_87021734 m1A Human chr2 + 111120965 111120965 111120965 CCTGGTCTGCAGTTTGTTGGAGCTCTGCGTCCAGCGCCGCTGCCGCTGCCGCCGCCGCCGCCGCC CCTGGTCTGCAGTTTGTTGGAGCTCTGCGTCCCGCGCCGCTGCCGCTGCCGCCGCCGCCGCCGCC A C BCL2L11 Ensembl:ENSG00000153094 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:111120914..111121180 26863196 MeRIP-seq:(Medium) rs998915916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622618,Human_RBP_ID_9330627,Human_RBP_ID_18442358 91159 RMVar_ID_91159 Human_SNP_ID_87021759 m1A Human chr2 - 111120979 111120976 111120979 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCGCTGGACGCAGAGCTCCAACA GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC___GGCAGCGGCGCTGGACGCAGAGCTCCAACA CGCT C MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:111120948..111121175;chr2:111120931..111121119 26863196 MeRIP-seq:(Medium) rs1305190668 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91160 RMVar_ID_91160 Human_SNP_ID_87021761 m1A Human chr2 - 111120979 111120979 111120979 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCGCTGGACGCAGAGCTCCAACA GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGCTGGACGCAGAGCTCCAACA T C MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:111120948..111121175;chr2:111120931..111121119 26863196 MeRIP-seq:(Medium) rs1188616075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91161 RMVar_ID_91161 Human_SNP_ID_87021839 m1A Human chr2 + 111121022 111121022 111121022 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACTACCACCACTTGATTCTTGCAGCCACCCTGC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTACCACCACTTGATTCTTGCAGCCACCCTGC A G BCL2L11 Ensembl:ENSG00000153094 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr2:111120969..111121070 26863410 MeRIP-seq:(Medium) rs950953725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623561,Human_RBP_ID_9330628 91162 RMVar_ID_91162 Human_SNP_ID_87021853 m1A Human chr2 + 111121044 111121044 111121044 CGCCGCCGCCACTACCACCACTTGATTCTTGCAGCCACCCTGCGAACCCTGCCACACTGCGATCG CGCCGCCGCCACTACCACCACTTGATTCTTGCCGCCACCCTGCGAACCCTGCCACACTGCGATCG A C BCL2L11 Ensembl:ENSG00000153094 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,total RNA Untreated chr2:111120940..111121138;chr2:111120943..111121175;chr2:111120938..111121188 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1171519425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623561,Human_RBP_ID_6813721,Human_RBP_ID_9330628,Human_RBP_ID_18744360 91163 RMVar_ID_91163 Human_SNP_ID_87022481 m1A Human chr2 - 111122659 111122659 111122659 TGGCCCGCGCTGCCCCGGCCGCAGCCGCCGGGAACATCCTCCGCCTCCTCCCGCTCCTCCCCTCG TGGCCCGCGCTGCCCCGGCCGCAGCCGCCGGGCACATCCTCCGCCTCCTCCCGCTCCTCCCCTCG T G MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:111122617..111123757 26863196 MeRIP-seq:(Medium) rs1403235839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91164 RMVar_ID_91164 Human_SNP_ID_87022917 m1A Human chr2 - 111123677 111123677 111123677 ATTATTTTAAGCAAAAAAAAAAATCGATGAATAAACAAATTAGCTCTCACCTAGCGATTAAAAAT ATTATTTTAAGCAAAAAAAAAAATCGATGAATGAACAAATTAGCTCTCACCTAGCGATTAAAAAT T C MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:111123672..111123758 26863196 MeRIP-seq:(Medium) rs1368886779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91165 RMVar_ID_91165 Human_SNP_ID_87046228 m1A Human chr2 + 111216855 111216855 111216855 CCCTGTCCCCCTGGCTGCTGGCACCAAGAGGCACCTGCAGGCCAGCACTGAGCAATCCTCAGAGC CCCTGTCCCCCTGGCTGCTGGCACCAAGAGGCCCCTGCAGGCCAGCACTGAGCAATCCTCAGAGC A C lnc-BCL2L11-6-002,lnc-BCL2L11-6-002:2,lnc-BCL2L11-6-001,lnc-BCL2L11-6-001:2 RNACentral:URS00009ADAD3,RNACentral:URS00009C2285,RNACentral:URS00008BF20F,RNACentral:URS00008B6560 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:111216809..111216892 26863196 MeRIP-seq:(Medium) rs1033116866 Functional Loss SNV dbSNP153 33..33 33 - - - 91166 RMVar_ID_91166 Human_SNP_ID_87246118 m1A Human chr2 - 112053477 112053477 112053477 TGAAATCGTTTTAGTTACGAGAGAACTGGAGGAATGGAAAGATCTTCCAGATGACTGGATGTTGG TGAAATCGTTTTAGTTACGAGAGAACTGGAGGCATGGAAAGATCTTCCAGATGACTGGATGTTGG T G AC093675.1 Ensembl:ENSG00000286904 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112053427..112053492 26863196 MeRIP-seq:(Medium) rs1439745106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91167 RMVar_ID_91167 Human_SNP_ID_87246377 m1A Human chr2 - 112054395 112054395 112054395 CGTAGTGGGGAGGCCAGGTTGGGCGAGGAAGCAGGGCTTGGAGCAAGCCCTAGTACGGAGACGGG CGTAGTGGGGAGGCCAGGTTGGGCGAGGAAGCCGGGCTTGGAGCAAGCCCTAGTACGGAGACGGG T G AC093675.1 Ensembl:ENSG00000286904 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112054345..112054490 26863196 MeRIP-seq:(Medium) rs939271675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91168 RMVar_ID_91168 Human_SNP_ID_87246475 m1A Human chr2 + 112054589 112054589 112054589 GGGTCTTGCCTCCAAATCCCGGCCCCGCCTCCACGCGGCCCCGCCTCCACGCGGCCCCGCCTCCA GGGTCTTGCCTCCAAATCCCGGCCCCGCCTCCCCGCGGCCCCGCCTCCACGCGGCCCCGCCTCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:112054541..112054634;chr2:112054218..112054633 26863196 MeRIP-seq:(Medium) rs1299840136 Functional Loss SNV dbSNP153 33..33 33 - - - 91169 RMVar_ID_91169 Human_SNP_ID_87246663 m1A Human chr2 + 112055014 112055014 112055014 CACGGCCCCGCCTCCACGCTCGGCCTGGCCCCAAGCTCTTCCTTCCTGGGGCACCCTGCCTCCGC CACGGCCCCGCCTCCACGCTCGGCCTGGCCCCCAGCTCTTCCTTCCTGGGGCACCCTGCCTCCGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112054965..112055115 26863196 MeRIP-seq:(Medium) rs1309065271 Functional Loss SNV dbSNP153 33..33 33 - - - 91170 RMVar_ID_91170 Human_SNP_ID_87246695 m1A Human chr2 + 112055102 112055102 112055102 GCCCCGCCTCCACAGTCCCGAGCCCGCCTCCAACCCTGCCCTGTCCCCACACCCAGCTTGGCCCC GCCCCGCCTCCACAGTCCCGAGCCCGCCTCCACCCCTGCCCTGTCCCCACACCCAGCTTGGCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112055040..112055115 26863196 MeRIP-seq:(Medium) rs1183104206 Functional Loss SNV dbSNP153 33..33 33 - - - 91171 RMVar_ID_91171 Human_SNP_ID_87266694 m1A Human chr2 - 112138732 112138732 112138732 CACTGGCCTGGAGAGAGGCGGGAGGGACACTGACCTGGGAAGCCCGCGGCTCGGGGCAGGCGAGG CACTGGCCTGGAGAGAGGCGGGAGGGACACTGGCCTGGGAAGCCCGCGGCTCGGGGCAGGCGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112138719..112138950 26863196 MeRIP-seq:(Medium) rs1217247969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91172 RMVar_ID_91172 Human_SNP_ID_87267025 m1A Human chr2 - 112140076 112140076 112140076 GCGGGAGGGACGCTGGCGTGGAGAGAGGCGGGAGGGACGCTGGCGTGGAGAGAGGCGGGAGGGAC GCGGGAGGGACGCTGGCGTGGAGAGAGGCGGGGGGGACGCTGGCGTGGAGAGAGGCGGGAGGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112140069..112140134 26863196 MeRIP-seq:(Medium) rs1412613877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91173 RMVar_ID_91173 Human_SNP_ID_87275108 m1A Human chr2 + 112171183 112171183 112171183 GGTAGACATCGTCTGGAGCTCAAGGCAGCAGAAGGGTTGGAGGTACCCAGTTGGGAGTTATTTGC GGTAGACATCGTCTGGAGCTCAAGGCAGCAGACGGGTTGGAGGTACCCAGTTGGGAGTTATTTGC A C FBLN7 Ensembl:ENSG00000144152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112171178..112171458 26863196 MeRIP-seq:(Medium) rs939881265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202622,RMVar_hsa_circ_331052,RMVar_hsa_circ_352167,RMVar_hsa_circ_73515,RMVar_hsa_circ_267475 91174 RMVar_ID_91174 Human_SNP_ID_87275132 m1A Human chr2 + 112171309 112171309 112171309 AGAAACGTGACTCAGGCAGAGACCTGCAGGGCACTGAGAAGTCAAATGGAGAAGGAGGAGGGCGA AGAAACGTGACTCAGGCAGAGACCTGCAGGGCGCTGAGAAGTCAAATGGAGAAGGAGGAGGGCGA A G FBLN7 Ensembl:ENSG00000144152 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112171287..112171377 26863196 MeRIP-seq:(Medium) rs944467128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202622,RMVar_hsa_circ_331052,RMVar_hsa_circ_352167,RMVar_hsa_circ_73515,RMVar_hsa_circ_267475 91175 RMVar_ID_91175 Human_SNP_ID_87298545 m1A Human chr2 - 112275268 112275267 112275268 CGCGGTTTTTCCTGCGAGACGCCCGCCGCCCGAGGAGTTCCAGACGCACCAAGCAAACGGGCCCC CGCGGTTTTTCCTGCGAGACGCCCGCCGCCCG_GGAGTTCCAGACGCACCAAGCAAACGGGCCCC CT C lnc-ZC3H8-7,lnc-ZC3H8-7:2 RNACentral:URS0000D5A3CE,RNACentral:URS0000D5C587 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112275222..112275405 26863196 MeRIP-seq:(Medium) rs1237974515 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91176 RMVar_ID_91176 Human_SNP_ID_87298554 m1A Human chr2 - 112275282 112275282 112275282 GGCGCAGTACGGGCCGCGGTTTTTCCTGCGAGACGCCCGCCGCCCGAGGAGTTCCAGACGCACCA GGCGCAGTACGGGCCGCGGTTTTTCCTGCGAGGCGCCCGCCGCCCGAGGAGTTCCAGACGCACCA T C lnc-ZC3H8-7,lnc-ZC3H8-7:2 RNACentral:URS0000D5A3CE,RNACentral:URS0000D5C587 lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:112275235..112275397 26863196 MeRIP-seq:(Medium) rs1312865091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 91177 RMVar_ID_91177 Human_SNP_ID_87304891 m1A Human chr2 + 112299930 112299930 112299930 GAAATACAAGAAAAAGAAGCAAAAGAGAATGAAAAGCAGAAAAGTGAGAAAGCCTACAGAAAATC GAAATACAAGAAAAAGAAGCAAAAGAGAATGAGAAGCAGAAAAGTGAGAAAGCCTACAGAAAATC A G ZC3H6 Ensembl:ENSG00000188177 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:112299849..112300050 26863196 MeRIP-seq:(Medium) rs1285002184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27818840 Human_Splice_Rec_288724,Human_Splice_Rec_288725,Human_Splice_Rec_288744,Human_Splice_Rec_288745,Human_Splice_Rec_288763 Human_miRNA_ID_201395 RMVar_hsa_circ_59090,RMVar_hsa_circ_271068,RMVar_hsa_circ_286918,RMVar_hsa_circ_340045,RMVar_hsa_circ_357555,RMVar_hsa_circ_323132,RMVar_hsa_circ_276533,RMVar_hsa_circ_74783,RMVar_hsa_circ_269195,RMVar_hsa_circ_69418,RMVar_hsa_circ_202628,RMVar_hsa_circ_202630,RMVar_hsa_circ_202631,RMVar_hsa_circ_202629,RMVar_hsa_circ_202627 91178 RMVar_ID_91178 Human_SNP_ID_87335465 m1A Human chr2 - 112433364 112433364 112433364 CCGTCGCCTCGACAGGTGAGTGGGTCTGGAAGAGAGCGGCGGCCTCGACCCGGCCGGGCGGCGGC CCGTCGCCTCGACAGGTGAGTGGGTCTGGAAGGGAGCGGCGGCCTCGACCCGGCCGGGCGGCGGC T C RGPD8 Ensembl:ENSG00000169629 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112433322..112433387 26863196 MeRIP-seq:(Medium) rs1206573109 Functional Loss SNV dbSNP153 33..33 33 - - - 91179 RMVar_ID_91179 Human_SNP_ID_87336297 m1A Human chr2 - 112436187 112436187 112436187 GGCAGGGTCATTCGTCATCACCTGGGTGCCCGAGGACGAGCAGGCTGCCCTGACGAGGATGATCA GGCAGGGTCATTCGTCATCACCTGGGTGCCCGTGGACGAGCAGGCTGCCCTGACGAGGATGATCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:112436141..112436337;chr2:112436140..112436285 26863196 MeRIP-seq:(Medium) rs1297212503 Functional Loss SNV dbSNP153 33..33 33 - - - 91180 RMVar_ID_91180 Human_SNP_ID_87347398 m1A Human chr2 + 112482171 112482171 112482171 GCGGGCGTGCGAGCGGCGCTTTCCTCTCCGGCACCCGGCGGGCGCCCGGGCGCGGCGCCGCCGGC GCGGGCGTGCGAGCGGCGCTTTCCTCTCCGGCCCCCGGCGGGCGCCCGGGCGCGGCGCCGCCGGC A C TTL Ensembl:ENSG00000114999 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112482134..112482215 26863196 MeRIP-seq:(Medium) rs1049615444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622624,Human_RBP_ID_5500665,Human_RBP_ID_18422315 91181 RMVar_ID_91181 Human_SNP_ID_87347424 m1A Human chr2 - 112482219 112482219 112482219 CCGCGGCCCGGCCCCCGCCGCCCGCGCCGGCTACCGCGCCTCTCGGGTGCCGGCGGCGCCGCGCC CCGCGGCCCGGCCCCCGCCGCCCGCGCCGGCTCCCGCGCCTCTCGGGTGCCGGCGGCGCCGCGCC T G HSALNG0017963 RNACentral:URS0000E95A39 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:112482133..112482354 26863410 MeRIP-seq:(Medium) rs1468066487 Functional Loss SNV dbSNP153 33..33 33 - - - 91182 RMVar_ID_91182 Human_SNP_ID_87347487 m1A Human chr2 + 112482345 112482345 112482345 TGCCCGGCGGCCCGGGCGCGCGGCGCTTCGCCATGTACACCTTCGTGGTACGCGATGAGAACAGC TGCCCGGCGGCCCGGGCGCGCGGCGCTTCGCCGTGTACACCTTCGTGGTACGCGATGAGAACAGC A G TTL Ensembl:ENSG00000114999 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112482130..112482447 26863196 MeRIP-seq:(Medium) rs1464116237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623567,Human_RBP_ID_26999620 91183 RMVar_ID_91183 Human_SNP_ID_87347488 m1A Human chr2 + 112482345 112482345 112482345 TGCCCGGCGGCCCGGGCGCGCGGCGCTTCGCCATGTACACCTTCGTGGTACGCGATGAGAACAGC TGCCCGGCGGCCCGGGCGCGCGGCGCTTCGCCTTGTACACCTTCGTGGTACGCGATGAGAACAGC A T TTL Ensembl:ENSG00000114999 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112482130..112482447 26863196 MeRIP-seq:(Medium) rs1464116237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623567,Human_RBP_ID_26999620 91184 RMVar_ID_91184 Human_SNP_ID_87358569 m1A Human chr2 + 112530250 112530250 112530250 CAATGCCTCCTTGAACATGATGAGATGTGAGAACTTACAATGAAAAAGGCAATAATGATAGAAAT CAATGCCTCCTTGAACATGATGAGATGTGAGAGCTTACAATGAAAAAGGCAATAATGATAGAAAT A G TTL Ensembl:ENSG00000114999 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:112530202..112530303 32194978 MeRIP-seq:(Medium) rs751150772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2579533,Human_RBP_ID_8841386,Human_RBP_ID_13581029,Human_RBP_ID_18309082 RMVar_hsa_circ_76778,RMVar_hsa_circ_202647,RMVar_hsa_circ_202648,RMVar_hsa_circ_110966,RMVar_hsa_circ_94831,RMVar_hsa_circ_202653 91185 RMVar_ID_91185 Human_SNP_ID_87361581 m1A Human chr2 + 112542814 112542814 112542814 TTGGTGGGTAAGCGGGAGAGCACAACATGTTAAACAGGACGCGGTACTGGCCTTCGTGAGACTTG TTGGTGGGTAAGCGGGAGAGCACAACATGTTACACAGGACGCGGTACTGGCCTTCGTGAGACTTG A C POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:112542676..112542915 26863196 MeRIP-seq:(Medium) rs1482835255 Functional Loss SNV dbSNP153 33..33 33 - - - 91186 RMVar_ID_91186 Human_SNP_ID_87369857 m1A Human chr2 + 112576600 112576600 112576600 TATTACAGATATCTCATATAGTGGGATCATGCAATATTTGTCCTGTGACTGGCTTATTTCACTTA TATTACAGATATCTCATATAGTGGGATCATGCGATATTTGTCCTGTGACTGGCTTATTTCACTTA A G POLR1B Ensembl:ENSG00000125630 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs986165962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_269041,Human_miRNA_ID_685576,Human_miRNA_ID_888124,Human_miRNA_ID_1064764,Human_miRNA_ID_1076078,Human_miRNA_ID_2625682,Human_miRNA_ID_2746502,Human_miRNA_ID_2776545 RMVar_hsa_circ_82908,RMVar_hsa_circ_202659,RMVar_hsa_circ_118343,RMVar_hsa_circ_87156,RMVar_hsa_circ_202665,RMVar_hsa_circ_202668,RMVar_hsa_circ_202669 91187 RMVar_ID_91187 Human_SNP_ID_87371795 m1A Human chr2 + 112584518 112584518 112584518 GGTAGGGCGCCGCCGTGACAGATTAGTCCTAAAGGGAACGGGGTTGTTAGTTCAATTGGCTACCG GGTAGGGCGCCGCCGTGACAGATTAGTCCTAATGGGAACGGGGTTGTTAGTTCAATTGGCTACCG A T CHCHD5 Ensembl:ENSG00000125611 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:112584477..112584587 26863196 MeRIP-seq:(Medium) rs751977664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_532502 91188 RMVar_ID_91188 Human_SNP_ID_87387272 m1A Human chr2 - 112645971 112645969 112645972 CAGCCGCGGGGGTTTCAGCGGCCGAGAAGAAGAACCACGCAGAGAGCGCCGGCAGCCATCACTCC CAGCCGCGGGGGTTTCAGCGGCCGAGAAGAA___CCACGCAGAGAGCGCCGGCAGCCATCACTCC GTTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:112645854..112646639;chr2:112645856..112646589 26863196 MeRIP-seq:(Medium) rs531708471 Functional Loss DEL dbSNP153 32..34 33 - - - 91189 RMVar_ID_91189 Human_SNP_ID_87387287 m1A Human chr2 - 112646002 112646002 112646002 GCTCAGCGGGACTCACGACCTTCCCAGGAAGCAGCCGCGGGGGTTTCAGCGGCCGAGAAGAAGAA GCTCAGCGGGACTCACGACCTTCCCAGGAAGCGGCCGCGGGGGTTTCAGCGGCCGAGAAGAAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112645881..112646245 26863196 MeRIP-seq:(Medium) rs995754382 Functional Loss SNV dbSNP153 33..33 33 - - - 91190 RMVar_ID_91190 Human_SNP_ID_87387320 m1A Human chr2 - 112646110 112646110 112646110 CGCCACTACTCACCAGGGAAAAGGGAGGGCGGAGCGGGAGACGAGGAGATCGAGGCGACAGCGGC CGCCACTACTCACCAGGGAAAAGGGAGGGCGGGGCGGGAGACGAGGAGATCGAGGCGACAGCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112645953..112646644 26863196 MeRIP-seq:(Medium) rs1351938807 Functional Loss SNV dbSNP153 33..33 33 - - - 91191 RMVar_ID_91191 Human_SNP_ID_87387522 m1A Human chr2 + 112646567 112646567 112646567 CTATTGTTATTTCCCCCCTCCCCCGCAGGATGAACTTGCGTCCTTTCTCTTCTCCGCCATGGAAT CTATTGTTATTTCCCCCCTCCCCCGCAGGATGCACTTGCGTCCTTTCTCTTCTCCGCCATGGAAT A C SLC20A1 Ensembl:ENSG00000144136 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:112646551..112646575 26863196 MeRIP-seq:(Medium) rs1028607443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_922619,Human_RBP_ID_4578458,Human_RBP_ID_18744602,Human_RBP_ID_18949487,Human_RBP_ID_23818942,Human_RBP_ID_25576794 Human_Splice_Rec_289240 RMVar_hsa_circ_73199,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_323789 91192 RMVar_ID_91192 Human_SNP_ID_87391051 m1A Human chr2 - 112659274 112659274 112659274 TCCTTATGCACGGTGTGATACTGGTAGTGGCCACTGGAGTTTATTTGGTTGCTGACGGCTTGACT TCCTTATGCACGGTGTGATACTGGTAGTGGCCGCTGGAGTTTATTTGGTTGCTGACGGCTTGACT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:112659225..112660597 32194978 MeRIP-seq:(Medium) rs1224029892 Functional Loss SNV dbSNP153 33..33 33 - - - 91193 RMVar_ID_91193 Human_SNP_ID_87411391 m1A Human chr2 - 112736943 112736943 112736943 CAGCCTGGGTTACAGAGCAAGACTCCATCTCAAAAAAAAAAAAGATGAAATCATCACCTCATAAA CAGCCTGGGTTACAGAGCAAGACTCCATCTCAGAAAAAAAAAAGATGAAATCATCACCTCATAAA T C CKAP2L Ensembl:ENSG00000169607 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4261731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_183623 91194 RMVar_ID_91194 Human_SNP_ID_87512089 m1A Human chr2 + 113157461 113157461 113157461 GCAGCCGAGGCCCCGCAGCTCTCGCCGCCCCCAGCCGGCGCCTGGGCGCGGGGCCGTGGGGCGCG GCAGCCGAGGCCCCGCAGCTCTCGCCGCCCCCGGCCGGCGCCTGGGCGCGGGGCCGTGGGGCGCG A G PSD4 Ensembl:ENSG00000125637 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113157413..113157574 26863196 MeRIP-seq:(Medium) rs1313068725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422316 Human_Splice_Rec_289681 91195 RMVar_ID_91195 Human_SNP_ID_87513826 m1A Human chr2 + 113164351 113164351 113164351 GCCTCGAAGGATGAAGAGGACTGGGGAAGGAAATGGAGCTGTCCAAGAGGACGTATGAACATGCC GCCTCGAAGGATGAAGAGGACTGGGGAAGGAAGTGGAGCTGTCCAAGAGGACGTATGAACATGCC A G PSD4 Ensembl:ENSG00000125637 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113164341..113164525 26863196 MeRIP-seq:(Medium) rs1187014364 Functional Loss SNV dbSNP153 33..33 33 - - - 91196 RMVar_ID_91196 Human_SNP_ID_87513880 m1A Human chr2 - 113164553 113164553 113164553 ATCACTCCTGTCCTAGAAAATCTTCACCTGGCACCCTCGTCCCCCATTCTCTAACAATGCCCCTA ATCACTCCTGTCCTAGAAAATCTTCACCTGGCGCCCTCGTCCCCCATTCTCTAACAATGCCCCTA T C lnc-PAX8-2 RNACentral:URS0000D5A738 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113164323..113164596 26863196 MeRIP-seq:(Medium) rs1262347894 Functional Loss SNV dbSNP153 33..33 33 - - - 91197 RMVar_ID_91197 Human_SNP_ID_87513930 m1A Human chr2 + 113164773 113164773 113164773 AAGGTTGCTAACTTGGGAAGCTGGTGGATGTGATGCCAGTCTAGACAGGTCCTGGGAGGGGCAGG AAGGTTGCTAACTTGGGAAGCTGGTGGATGTGCTGCCAGTCTAGACAGGTCCTGGGAGGGGCAGG A C PSD4 Ensembl:ENSG00000125637 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113164723..113164789 26863196 MeRIP-seq:(Medium) rs933557420 Functional Loss SNV dbSNP153 33..33 33 - - - 91198 RMVar_ID_91198 Human_SNP_ID_87522705 m1A Human chr2 - 113198982 113198982 113198982 GCCGCCCCCCTGGCCGCCTCGGTTCCCAGGCCAAGTGCGCAGCCCGCCTCCAGCCTCCCCGAGTT GCCGCCCCCCTGGCCGCCTCGGTTCCCAGGCCTAGTGCGCAGCCCGCCTCCAGCCTCCCCGAGTT T A lnc-PAX8-2 RNACentral:URS0000D5A738 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113198933..113199261 26863196 MeRIP-seq:(Medium) rs898088992 Functional Loss SNV dbSNP153 33..33 33 - - - 91199 RMVar_ID_91199 Human_SNP_ID_87524162 m1A Human chr2 - 113204859 113204859 113204859 CGGCCCTGTTTCCCTCTGCCCCCCTCACCCCGACCCTCCAGTCCTGCTCCTTCCAACCCCGACAC CGGCCCTGTTTCCCTCTGCCCCCCTCACCCCGCCCCTCCAGTCCTGCTCCTTCCAACCCCGACAC T G lnc-PAX8-2 RNACentral:URS0000D5A738 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113204812..113204919 26863196 MeRIP-seq:(Medium) rs926531817 Functional Loss SNV dbSNP153 33..33 33 - - - 91200 RMVar_ID_91200 Human_SNP_ID_87528543 m1A Human chr2 - 113224585 113224585 113224585 CCGTCATCCTCCACCTTTCCACCGATCCTTCCATCTTTCCATCCATCTTTCCTTTTTTTTTTTTT CCGTCATCCTCCACCTTTCCACCGATCCTTCCGTCTTTCCATCCATCTTTCCTTTTTTTTTTTTT T C PAX8 Ensembl:ENSG00000125618 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:113224497..113224584 26863410 MeRIP-seq:(Medium) rs979873446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280278,Human_RBP_ID_6815469,Human_RBP_ID_8104131,Human_RBP_ID_17697057,Human_RBP_ID_17938359,Human_RBP_ID_18208721,Human_RBP_ID_24533257,Human_RBP_ID_27474372 91201 RMVar_ID_91201 Human_SNP_ID_87531257 m1A Human chr2 - 113235671 113235671 113235671 GGGCAGCTGAGCCTGCCCCGCGCCCCGCCCGCACCCTCCACATCCCACGGCTTGGCTTGTGCGTG GGGCAGCTGAGCCTGCCCCGCGCCCCGCCCGCCCCCTCCACATCCCACGGCTTGGCTTGTGCGTG T G PAX8 Ensembl:ENSG00000125618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113235633..113235800 26863196 MeRIP-seq:(Medium) rs895266697 Functional Loss SNV dbSNP153 33..33 33 - - - 91202 RMVar_ID_91202 Human_SNP_ID_87552221 m1A Human chr2 - 113324676 113324676 113324676 GAGAGGAGAAAATGAATCCAAAGAGGATGCAAAAAAGGAGGAAGGAGAGATGTCTGGTAGAGAGG GAGAGGAGAAAATGAATCCAAAGAGGATGCAATAAAGGAGGAAGGAGAGATGTCTGGTAGAGAGG T A lnc-PAX8-2 RNACentral:URS0000D5A738 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:113324639..113324802 26863196 MeRIP-seq:(Medium) rs77529563 Functional Loss SNV dbSNP153 33..33 33 - - - 91203 RMVar_ID_91203 Human_SNP_ID_87552236 m1A Human chr2 - 113324770 113324770 113324770 AGCAAAGGGAGAGGGAGAGACTGAAGAGAGGAACGGAAAAGACTGGAAAAGACAGCAAGGGGTGA AGCAAAGGGAGAGGGAGAGACTGAAGAGAGGAGCGGAAAAGACTGGAAAAGACAGCAAGGGGTGA T C lnc-PAX8-2 RNACentral:URS0000D5A738 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113324626..113324897 26863196 MeRIP-seq:(Medium) rs961155927 Functional Loss SNV dbSNP153 33..33 33 - - - 91204 RMVar_ID_91204 Human_SNP_ID_87552346 m1A Human chr2 + 113325151 113325151 113325151 TCTGGGAGGCAGGCGTGGGGGTCGGGTGTCGGAGGCCCCGTGCGCCCCCCCACCCCCCACCAGAG TCTGGGAGGCAGGCGTGGGGGTCGGGTGTCGGCGGCCCCGTGCGCCCCCCCACCCCCCACCAGAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:113325104..113325229 26863196 MeRIP-seq:(Medium) rs1231716491 Functional Loss SNV dbSNP153 33..33 33 - - - 91205 RMVar_ID_91205 Human_SNP_ID_87552432 m1A Human chr2 + 113325552 113325552 113325552 GATGGGAAGGGGAGAAACAGAAGAGTGTGACGAGGTGGGTGTCCAAGGGCAATGGGACAGGCAGT GATGGGAAGGGGAGAAACAGAAGAGTGTGACGGGGTGGGTGTCCAAGGGCAATGGGACAGGCAGT A G AC016745.1 Ensembl:ENSG00000234997 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113325516..113325600 26863196 MeRIP-seq:(Medium) rs1312192526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_290181 91206 RMVar_ID_91206 Human_SNP_ID_87558127 m1A Human chr2 + 113352159 113352159 113352159 AGGAACCAACAACAAGGGGACAGGGAGAGAGCACACTGACTGAGGGGACGGGGGAAATCAGGAAG AGGAACCAACAACAAGGGGACAGGGAGAGAGCTCACTGACTGAGGGGACGGGGGAAATCAGGAAG A T AC016745.1 Ensembl:ENSG00000234997 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113352141..113352214 26863196 MeRIP-seq:(Medium) rs1357543346 Functional Loss SNV dbSNP153 33..33 33 - - - 91207 RMVar_ID_91207 Human_SNP_ID_87577589 m1A Human chr2 + 113437945 113437945 113437945 GGAGGAGGATTGTCCTGAATTGGTTCCCATGGAGACGACGCAAAGCGAGGAGGAGGAAAAGTCTG GGAGGAGGATTGTCCTGAATTGGTTCCCATGGGGACGACGCAAAGCGAGGAGGAGGAAAAGTCTG A G CBWD2 Ensembl:ENSG00000136682 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113437881..113438000 26863196 MeRIP-seq:(Medium) rs771048315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_532634,Human_RBP_ID_6815518,Human_RBP_ID_13583264 Human_Splice_Rec_290191,Human_Splice_Rec_290219,Human_Splice_Rec_290245,Human_Splice_Rec_290273,Human_Splice_Rec_290303,Human_Splice_Rec_290305,Human_Splice_Rec_290335,Human_Splice_Rec_290339 91208 RMVar_ID_91208 Human_SNP_ID_87612826 m1A Human chr2 + 113583962 113583962 113583962 TGAGTTCCGTGCCCAGGCCCGCGACTCGGTCCACCAGGACAGCGCTCCGGGTCGACGGGGTCCTG TGAGTTCCGTGCCCAGGCCCGCGACTCGGTCCGCCAGGACAGCGCTCCGGGTCGACGGGGTCCTG A G lnc-RABL2A-7 RNACentral:URS00008C0EFB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113583911..113584017 26863196 MeRIP-seq:(Medium) rs2418696 Functional Loss SNV dbSNP153 33..33 33 - - - 91209 RMVar_ID_91209 Human_SNP_ID_87615279 m1A Human chr2 + 113591550 113591550 113591550 TCCTGGAAGAGGGGGGCAGGGTAGGGAGGTGGATATGCAGGTTGCCCTGGTGGGGTCTGGAAATG TCCTGGAAGAGGGGGGCAGGGTAGGGAGGTGGGTATGCAGGTTGCCCTGGTGGGGTCTGGAAATG A G WASH2P Ensembl:ENSG00000146556 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:113591501..113591604 26863196 MeRIP-seq:(Medium) rs1318688501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_264394,Human_RBP_ID_5239659,Human_RBP_ID_8109923,Human_RBP_ID_9429706,Human_RBP_ID_25456419,Human_RBP_ID_26786442 91210 RMVar_ID_91210 Human_SNP_ID_87615414 m1A Human chr2 - 113591941 113591941 113591941 CCCTGCTCAAAATCCAATCACAGCTCCCTAACACTCCTGAATCAACGTGAAGTCCTGTCTTGAGT CCCTGCTCAAAATCCAATCACAGCTCCCTAACGCTCCTGAATCAACGTGAAGTCCTGTCTTGAGT T C lnc-SLC35F5-17 RNACentral:URS00008BF43D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:113591912..113591977;chr2:113591895..113591984;chr2:113591901..113592104 26863196 MeRIP-seq:(Medium) rs7566588 Functional Loss SNV dbSNP153 33..33 33 - - - 91211 RMVar_ID_91211 Human_SNP_ID_87616882 m1A Human chr2 + 113596805 113596805 113596805 CCCCTGTAGGCCAAGGCGCCAGGCAGGACGACAGCAGCAGCAGCGCGTCTCCTTCAGGTGGGAGC CCCCTGTAGGCCAAGGCGCCAGGCAGGACGACGGCAGCAGCAGCGCGTCTCCTTCAGGTGGGAGC A G WASH2P Ensembl:ENSG00000146556 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1178326930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_148242,Human_RBP_ID_919910 Human_Splice_Rec_290427,Human_Splice_Rec_290441 91212 RMVar_ID_91212 Human_SNP_ID_87626576 m1A Human chr2 + 113625646 113625646 113625646 AAATGTCTCCCAAATCCACTTCTCTCCCTTCAATGTCCAGGCCACCAGCATGACTTCTGCATGTG AAATGTCTCCCAAATCCACTTCTCTCCCTTCACTGTCCAGGCCACCAGCATGACTTCTGCATGTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:113625643..113626843;chr2:113625546..113625710 26863196 MeRIP-seq:(Medium) rs2592690 Functional Loss SNV dbSNP153 33..33 33 - - - 91213 RMVar_ID_91213 Human_SNP_ID_87626905 m1A Human chr2 + 113627079 113627079 113627079 CCCTCTAGGCGGGCGGCACCCGCTGAAGCCTCAGTACCACACCCACAGCCAGGAGCCCCAGTCCC CCCTCTAGGCGGGCGGCACCCGCTGAAGCCTCGGTACCACACCCACAGCCAGGAGCCCCAGTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:113627026..113627106;chr2:113627004..113627112;chr2:113626970..113627099 26863196 MeRIP-seq:(Medium) rs2519465 Functional Loss SNV dbSNP153 33..33 33 - - - 91214 RMVar_ID_91214 Human_SNP_ID_87627001 m1A Human chr2 - 113627306 113627306 113627306 CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCACCCCGCCGGCCCAGCTCGCACCGCAGCGCACT CCGCCAGTCTGGACTCTGCGCGCTCTCGAACCCCCCCGCCGGCCCAGCTCGCACCGCAGCGCACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:113627283..113627351;chr2:113627286..113627376;chr2:113627283..113627370 26863196 MeRIP-seq:(Medium) rs932922963 Functional Loss SNV dbSNP153 33..33 33 - - - 91215 RMVar_ID_91215 Human_SNP_ID_87628725 m1A Human chr2 + 113634304 113634304 113634304 AGAGGAAATGGGAGACGAGGGGAGGTGAGGCAAGGTTCATAAGGAGAGAGTCCAGAGGGAGAAAA AGAGGAAATGGGAGACGAGGGGAGGTGAGGCAGGGTTCATAAGGAGAGAGTCCAGAGGGAGAAAA A G RABL2A Ensembl:ENSG00000144134 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113634231..113634350 26863196 MeRIP-seq:(Medium) rs1023636550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923650 RMVar_hsa_circ_5054,RMVar_hsa_circ_77687,RMVar_hsa_circ_202692,RMVar_hsa_circ_110842,RMVar_hsa_circ_282657,RMVar_hsa_circ_202693,RMVar_hsa_circ_202694 91216 RMVar_ID_91216 Human_SNP_ID_87647333 m1A Human chr2 - 113708487 113708484 113708487 TTGGCCAGGTTGGTCTTGAACTCTTGACCTCAAGTGATCTACACGCCTCGGCCTCCCAAAGTGCT TTGGCCAGGTTGGTCTTGAACTCTTGACCTCA___GATCTACACGCCTCGGCCTCCCAAAGTGCT CACT C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1313085698 Functional Loss DEL dbSNP153 33..35 33 - - - 91217 RMVar_ID_91217 Human_SNP_ID_87647407 m1A Human chr2 - 113708721 113708721 113708721 ATAGCATGTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTC ATAGCATGTAATTATGCAGTATTTTATTTTTTGTTTTTTATTTTTTTTGAGACAGAGTCTCACTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs766022823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6815683 91218 RMVar_ID_91218 Human_SNP_ID_87648188 m1A Human chr2 - 113712428 113712428 113712428 CCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGCAGAATGGCGTGAACCCGGGAGGCGGAGCCT CCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCGGCAGAATGGCGTGAACCCGGGAGGCGGAGCCT T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1259683099 Functional Loss SNV dbSNP153 33..33 33 - - - 91219 RMVar_ID_91219 Human_SNP_ID_87658165 m1A Human chr2 - 113756390 113756390 113756390 GACCGGTCCGCTCATGGTGCCGCCACGACGCCATCGCGGGGCAGGAAGGCCAGGTAGGCAGGCAG GACCGGTCCGCTCATGGTGCCGCCACGACGCCGTCGCGGGGCAGGAAGGCCAGGTAGGCAGGCAG T C SLC35F5 Ensembl:ENSG00000115084 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:113756375..113756558 26863410 MeRIP-seq:(Medium) rs1367133870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830395,Human_RBP_ID_4622633,Human_RBP_ID_22450525 Human_Splice_Rec_290665,Human_Splice_Rec_290773 RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202724,RMVar_hsa_circ_122710 91220 RMVar_ID_91220 Human_SNP_ID_87658206 m1A Human chr2 + 113756468 113756468 113756468 GCCCAGCGCCACGGCCGCGGCCTCGGACTCACAGAGCTGTCACCGCGCCTGACATCGCGCCGCAC GCCCAGCGCCACGGCCGCGGCCTCGGACTCACGGAGCTGTCACCGCGCCTGACATCGCGCCGCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113756418..113756582 26863196 MeRIP-seq:(Medium) rs536549494 Functional Loss SNV dbSNP153 33..33 33 - - - 91221 RMVar_ID_91221 Human_SNP_ID_87697114 m1A Human chr2 + 113913154 113913148 113913155 ATAATTGCTAAAATATTAGTGAAATCTTTATAAATTATTTTGTTTTGCAGGTATACAAAACTAGG ATAATTGCTAAAATATTAGTGAAATCT_______TTATTTTGTTTTGCAGGTATACAAAACTAGG TTTATAAA T ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:113913151..113913225 26863196 MeRIP-seq:(Medium) rs1484836471 Functional Loss DEL dbSNP153 28..34 33 - - - Human_Splice_Rec_290803,Human_Splice_Rec_290825,Human_Splice_Rec_290833,Human_Splice_Rec_290845 91222 RMVar_ID_91222 Human_SNP_ID_87697117 m1A Human chr2 + 113913153 113913153 113913153 TATAATTGCTAAAATATTAGTGAAATCTTTATAAATTATTTTGTTTTGCAGGTATACAAAACTAG TATAATTGCTAAAATATTAGTGAAATCTTTATGAATTATTTTGTTTTGCAGGTATACAAAACTAG A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:113913151..113913250 26863196 MeRIP-seq:(Medium) rs1223606680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_290803,Human_Splice_Rec_290825,Human_Splice_Rec_290833,Human_Splice_Rec_290845 91223 RMVar_ID_91223 Human_SNP_ID_87697118 m1A Human chr2 + 113913154 113913154 113913154 ATAATTGCTAAAATATTAGTGAAATCTTTATAAATTATTTTGTTTTGCAGGTATACAAAACTAGG ATAATTGCTAAAATATTAGTGAAATCTTTATACATTATTTTGTTTTGCAGGTATACAAAACTAGG A C ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:113913151..113913225 26863196 MeRIP-seq:(Medium) rs1246807504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_290803,Human_Splice_Rec_290825,Human_Splice_Rec_290833,Human_Splice_Rec_290845 91224 RMVar_ID_91224 Human_SNP_ID_87704804 m1A Human chr2 - 113943476 113943476 113943476 ATGCTGCGAGAGTAACCTTTCTAATATGGTACACAATTATCTTCTATGCTTAAAATTTTTGCATG ATGCTGCGAGAGTAACCTTTCTAATATGGTACGCAATTATCTTCTATGCTTAAAATTTTTGCATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113943461..113943623 26863196 MeRIP-seq:(Medium) rs1559486080 Functional Loss SNV dbSNP153 33..33 33 - - - 91225 RMVar_ID_91225 Human_SNP_ID_88492381 m1A Human chr2 + 117023122 117023122 117023122 AGCAAATCATACCCTGACTGTTTACCAAAAACATCACCTCTAGCATTAACAGTATTAGAGGCACT AGCAAATCATACCCTGACTGTTTACCAAAAACGTCACCTCTAGCATTAACAGTATTAGAGGCACT A G RF02541-012,lnc-DDX18-9 RNACentral:URS0000905257,RNACentral:URS00008BE75F rRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr2:117023072..117023268;chr2:117023073..117023249 26863196 MeRIP-seq:(Medium) rs1191989530 Functional Loss SNV dbSNP153 33..33 33 - - - 91226 RMVar_ID_91226 Human_SNP_ID_88492400 m1A Human chr2 + 117023217 117023217 117023217 CAGTATCCTGACAGTGCACAGGTAGCATAATCACTTGTTCCCTAAATAGGGACTTGTATGAATGG CAGTATCCTGACAGTGCACAGGTAGCATAATCTCTTGTTCCCTAAATAGGGACTTGTATGAATGG A T RF02541-012,lnc-DDX18-9 RNACentral:URS0000905257,RNACentral:URS00008BE75F rRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:117023071..117023265;chr2:117023113..117023281 26863196 MeRIP-seq:(Medium) rs188613286 Functional Loss SNV dbSNP153 33..33 33 - - - 91227 RMVar_ID_91227 Human_SNP_ID_88708206 m1A Human chr2 - 117814737 117814737 117814737 ACAAGTGCCTAGAATAAGGCGCCACACAGTACAGCTACTCAGTTCTCAGGCTGACGTTACTTCCC ACAAGTGCCTAGAATAAGGCGCCACACAGTACCGCTACTCAGTTCTCAGGCTGACGTTACTTCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:117814676..117814875 26863196 MeRIP-seq:(Medium) rs766717725 Functional Loss SNV dbSNP153 33..33 33 - - - 91228 RMVar_ID_91228 Human_SNP_ID_88708211 m1A Human chr2 - 117814746 117814746 117814746 TTCTGCCCAACAAGTGCCTAGAATAAGGCGCCACACAGTACAGCTACTCAGTTCTCAGGCTGACG TTCTGCCCAACAAGTGCCTAGAATAAGGCGCCGCACAGTACAGCTACTCAGTTCTCAGGCTGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:117814701..117814850;chr2:117814701..117814825;chr2:117814701..117814819 26863196 MeRIP-seq:(Medium) rs368968488 Functional Loss SNV dbSNP153 33..33 33 - - - 91229 RMVar_ID_91229 Human_SNP_ID_88712740 m1A Human chr2 + 117830679 117830679 117830679 ACCAAGAAAGTTGAGAAATCCAAAATCTTTAAACACATTAGCAAGAAATCATCTGACAGCAGGCA ACCAAGAAAGTTGAGAAATCCAAAATCTTTAAGCACATTAGCAAGAAATCATCTGACAGCAGGCA A G DDX18 Ensembl:ENSG00000088205 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:117830589..117830839 32194978 MeRIP-seq:(Medium) rs1558735777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1896405,Human_RBP_ID_3593070,Human_RBP_ID_8257240,Human_RBP_ID_13588276,Human_RBP_ID_17273342,Human_RBP_ID_17938554,Human_RBP_ID_20451519,Human_RBP_ID_24485890 Human_Splice_Rec_291280,Human_Splice_Rec_291316 RMVar_hsa_circ_107155,RMVar_hsa_circ_202793,RMVar_hsa_circ_96522,RMVar_hsa_circ_76033,RMVar_hsa_circ_202794,RMVar_hsa_circ_202796,RMVar_hsa_circ_110900,RMVar_hsa_circ_202800,RMVar_hsa_circ_125012,RMVar_hsa_circ_202802 91230 RMVar_ID_91230 Human_SNP_ID_88713019 m1A Human chr2 - 117831932 117831932 117831932 TTTCTCTATATTCGATGTTAGCACACTTATTTAATGGGATCCTATGATTAACTGGCACAACAGCA TTTCTCTATATTCGATGTTAGCACACTTATTTTATGGGATCCTATGATTAACTGGCACAACAGCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:117831881..117832081 32194978 MeRIP-seq:(Medium) rs766320187 Functional Loss SNV dbSNP153 33..33 33 - - - 91231 RMVar_ID_91231 Human_SNP_ID_88722829 m1A Human chr2 - 117871116 117871108 117871116 GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGG GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGG________GAGGAGGAGGAGGAGGAGGCGGCGG CCTCCTCCT C lnc-CCDC93-4 RNACentral:URS00008BCC3B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:117871065..117871132 26863196 MeRIP-seq:(Medium) rs1434707474 Functional Loss DEL dbSNP153 33..40 33 - - - 91232 RMVar_ID_91232 Human_SNP_ID_88722839 m1A Human chr2 - 117871116 117871116 117871116 GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGG GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGGTGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGG T A lnc-CCDC93-4 RNACentral:URS00008BCC3B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:117871065..117871132 26863196 MeRIP-seq:(Medium) rs1319889606 Functional Loss SNV dbSNP153 33..33 33 - - - 91233 RMVar_ID_91233 Human_SNP_ID_88722840 m1A Human chr2 - 117871116 117871116 117871116 GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGG GGCGGTGGAGGAGGAGGAGGAGGAGGAGGAGGCGGAGGAGGAGGAGGAGGAGGAGGAGGCGGCGG T G lnc-CCDC93-4 RNACentral:URS00008BCC3B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:117871065..117871132 26863196 MeRIP-seq:(Medium) rs1319889606 Functional Loss SNV dbSNP153 33..33 33 - - - 91234 RMVar_ID_91234 Human_SNP_ID_88760363 m1A Human chr2 - 118013330 118013330 118013330 CGCGCCGGGGCGTTCGGGGTGGGACGCACTCCAGGGGTGCTGTGTGGCGGGGGACCCGGCTCTGG CGCGCCGGGGCGTTCGGGGTGGGACGCACTCCGGGGGTGCTGTGTGGCGGGGGACCCGGCTCTGG T C CCDC93 Ensembl:ENSG00000125633 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:118013328..118013403 26863196 MeRIP-seq:(Medium) rs754545628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26787127 RMVar_hsa_circ_119248,RMVar_hsa_circ_202804 91235 RMVar_ID_91235 Human_SNP_ID_88760657 m1A Human chr2 - 118014059 118014059 118014059 TTTGTACTCCACCCCGGTAGCAGCTCCGCGGCAGGGACAGCTTCCTCCGGACGCTTGGCGGGCTT TTTGTACTCCACCCCGGTAGCAGCTCCGCGGCGGGGACAGCTTCCTCCGGACGCTTGGCGGGCTT T C CCDC93 Ensembl:ENSG00000125633 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:118013904..118014085 26863196 MeRIP-seq:(Medium) rs1259910887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242703,Human_RBP_ID_5471438,Human_RBP_ID_9387317,Human_RBP_ID_22997195 RMVar_hsa_circ_119248,RMVar_hsa_circ_202804 91236 RMVar_ID_91236 Human_SNP_ID_88778309 m1A Human chr2 + 118089383 118089383 118089383 AAAAAGGAATGGTTAGGCTTGGCAGCTGGGCCACTGAAACTGTTTGGTATCAGTATTGCGGTGGA AAAAAGGAATGGTTAGGCTTGGCAGCTGGGCCGCTGAAACTGTTTGGTATCAGTATTGCGGTGGA A G INSIG2 Ensembl:ENSG00000125629 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:118089379..118089489 32194978 MeRIP-seq:(Medium) rs1187690574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827047,Human_RBP_ID_17137223,Human_RBP_ID_17670471 91237 RMVar_ID_91237 Human_SNP_ID_89072653 m1A Human chr2 - 119264617 119264617 119264617 TTCTGCAGAGGGTTGGGGGCTCAGCCGAGAACACCTGTTTCTTCACAGGGGAAGTAAGCTAGAGT TTCTGCAGAGGGTTGGGGGCTCAGCCGAGAACCCCTGTTTCTTCACAGGGGAAGTAAGCTAGAGT T G STEAP3-AS1 Ensembl:ENSG00000229867 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:119264566..119264655 26863196 MeRIP-seq:(Medium) rs905466027 Functional Loss SNV dbSNP153 33..33 33 - - - 91238 RMVar_ID_91238 Human_SNP_ID_89096071 m1A Human chr2 - 119367024 119367018 119367025 GACATCCTGGCCGACTTGCAAGAACTCCAGGGAGACAGCGGAGGAGGCGAGGACCAGGAAGCGAT GACATCCTGGCCGACTTGCAAGAACTCCAGG_______CGGAGGAGGCGAGGACCAGGAAGCGAT GCTGTCTC G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:119366976..119367075 32194978 MeRIP-seq:(Medium) rs767700430 Functional Loss DEL dbSNP153 32..38 33 - - - 91239 RMVar_ID_91239 Human_SNP_ID_89096181 m1A Human chr2 + 119367266 119367266 119367266 TGGGGATTTCTAAATCTGCTGCCCACCCCGCAACTGCCGGAAAGTTGCCCATGGGGTGGACTTCG TGGGGATTTCTAAATCTGCTGCCCACCCCGCAGCTGCCGGAAAGTTGCCCATGGGGTGGACTTCG A G DBI Ensembl:ENSG00000155368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:119367264..119367551 26863196 MeRIP-seq:(Medium) rs1281222201 Functional Loss SNV dbSNP153 33..33 33 - - - 91240 RMVar_ID_91240 Human_SNP_ID_89096193 m1A Human chr2 - 119367290 119367290 119367290 TCCCACCCCTCTCCCGCTACACAGCGAAGTCCACCCCATGGGCAACTTTCCGGCAGTTGCGGGGT TCCCACCCCTCTCCCGCTACACAGCGAAGTCCGCCCCATGGGCAACTTTCCGGCAGTTGCGGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:119367287..119367576 26863196 MeRIP-seq:(Medium) rs1274155573 Functional Loss SNV dbSNP153 33..33 33 - - - 91241 RMVar_ID_91241 Human_SNP_ID_89096578 m1A Human chr2 + 119368234 119368234 119368234 AGCTGCAGAGGAGGTTAGGCACCTTAAGACCAAGCCATCGGATGAGGAGATGCTGTTCATCTATG AGCTGCAGAGGAGGTTAGGCACCTTAAGACCACGCCATCGGATGAGGAGATGCTGTTCATCTATG A C DBI Ensembl:ENSG00000155368 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:119368176..119368325 32194978 MeRIP-seq:(Medium) rs373223217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61466,Human_RBP_ID_147175,Human_RBP_ID_1896536,Human_RBP_ID_4579280,Human_RBP_ID_9384609,Human_RBP_ID_17658594,Human_RBP_ID_22451575 Human_Splice_Rec_291786,Human_Splice_Rec_291787,Human_Splice_Rec_291794,Human_Splice_Rec_291795,Human_Splice_Rec_291800,Human_Splice_Rec_291801,Human_Splice_Rec_291806,Human_Splice_Rec_291810,Human_Splice_Rec_291811,Human_Splice_Rec_291818,Human_Splice_Rec_291819,Human_Splice_Rec_291824,Human_Splice_Rec_291825,Human_Splice_Rec_291832,Human_Splice_Rec_291833,Human_Splice_Rec_291838,Human_Splice_Rec_291839,Human_Splice_Rec_291844,Human_Splice_Rec_291845,Human_Splice_Rec_291850,Human_Splice_Rec_291851 Human_miRNA_ID_258244,Human_miRNA_ID_262039 91242 RMVar_ID_91242 Human_SNP_ID_89096579 m1A Human chr2 + 119368234 119368234 119368234 AGCTGCAGAGGAGGTTAGGCACCTTAAGACCAAGCCATCGGATGAGGAGATGCTGTTCATCTATG AGCTGCAGAGGAGGTTAGGCACCTTAAGACCAGGCCATCGGATGAGGAGATGCTGTTCATCTATG A G DBI Ensembl:ENSG00000155368 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:119368176..119368325 32194978 MeRIP-seq:(Medium) rs373223217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61466,Human_RBP_ID_147175,Human_RBP_ID_1896536,Human_RBP_ID_4579280,Human_RBP_ID_9384609,Human_RBP_ID_17658594,Human_RBP_ID_22451575 Human_Splice_Rec_291786,Human_Splice_Rec_291787,Human_Splice_Rec_291794,Human_Splice_Rec_291795,Human_Splice_Rec_291800,Human_Splice_Rec_291801,Human_Splice_Rec_291806,Human_Splice_Rec_291810,Human_Splice_Rec_291811,Human_Splice_Rec_291818,Human_Splice_Rec_291819,Human_Splice_Rec_291824,Human_Splice_Rec_291825,Human_Splice_Rec_291832,Human_Splice_Rec_291833,Human_Splice_Rec_291838,Human_Splice_Rec_291839,Human_Splice_Rec_291844,Human_Splice_Rec_291845,Human_Splice_Rec_291850,Human_Splice_Rec_291851 Human_miRNA_ID_258244,Human_miRNA_ID_262039 91243 RMVar_ID_91243 Human_SNP_ID_89096585 m1A Human chr2 + 119368246 119368246 119368246 GGTTAGGCACCTTAAGACCAAGCCATCGGATGAGGAGATGCTGTTCATCTATGGCCACTACAAAC GGTTAGGCACCTTAAGACCAAGCCATCGGATGGGGAGATGCTGTTCATCTATGGCCACTACAAAC A G DBI Ensembl:ENSG00000155368 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1277685829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147175,Human_RBP_ID_533173,Human_RBP_ID_4623588,Human_RBP_ID_9384610,Human_RBP_ID_17658594,Human_RBP_ID_17938696,Human_RBP_ID_22451575,Human_RBP_ID_26999972 Human_Splice_Rec_291786,Human_Splice_Rec_291787,Human_Splice_Rec_291794,Human_Splice_Rec_291795,Human_Splice_Rec_291800,Human_Splice_Rec_291801,Human_Splice_Rec_291806,Human_Splice_Rec_291810,Human_Splice_Rec_291811,Human_Splice_Rec_291818,Human_Splice_Rec_291819,Human_Splice_Rec_291824,Human_Splice_Rec_291825,Human_Splice_Rec_291832,Human_Splice_Rec_291833,Human_Splice_Rec_291838,Human_Splice_Rec_291839,Human_Splice_Rec_291844,Human_Splice_Rec_291845,Human_Splice_Rec_291850,Human_Splice_Rec_291851 91244 RMVar_ID_91244 Human_SNP_ID_89112244 m1A Human chr2 + 119431950 119431950 119431950 CGTGCAGGTAGCCGGCGCCTGGCGGGGCGCTGACCCGGGGTGCTGCCCCGCCGTGGGAGGTTGGG CGTGCAGGTAGCCGGCGCCTGGCGGGGCGCTGCCCCGGGGTGCTGCCCCGCCGTGGGAGGTTGGG A C TMEM37 Ensembl:ENSG00000171227 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:119431899..119432022 26863196 MeRIP-seq:(Medium) rs1165643057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19101491 91245 RMVar_ID_91245 Human_SNP_ID_89112586 m1A Human chr2 + 119433327 119433327 119433327 GGCAAACACAGGTAGGAAGCAAGTTCTGGGTCATGCAGGCAGCGGTGGGCCAGGCTGCAGCTGAG GGCAAACACAGGTAGGAAGCAAGTTCTGGGTCGTGCAGGCAGCGGTGGGCCAGGCTGCAGCTGAG A G TMEM37 Ensembl:ENSG00000171227 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:119433321..119433486 26863196 MeRIP-seq:(Medium) rs1472436882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23282733 91246 RMVar_ID_91246 Human_SNP_ID_89171939 m1A Human chr2 - 119679268 119679268 119679268 TACTCCGCAGTCTGAACGCGTTACCGGGTCGCATCAGGCCGGAGAAGGGTCCCTCCCGCTCGTCC TACTCCGCAGTCTGAACGCGTTACCGGGTCGCCTCAGGCCGGAGAAGGGTCCCTCCCGCTCGTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:119679220..119679386 26863196 MeRIP-seq:(Medium) rs1283639117 Functional Loss SNV dbSNP153 33..33 33 - - - 91247 RMVar_ID_91247 Human_SNP_ID_89172280 m1A Human chr2 - 119680843 119680843 119680843 TCCGCCACAGGGGACCTGCCATGAGTGTAGTCACTGCGGACAATCTGGGCCAAGAAAAAGAGAAG TCCGCCACAGGGGACCTGCCATGAGTGTAGTCGCTGCGGACAATCTGGGCCAAGAAAAAGAGAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:119680838..119680967 26863196 MeRIP-seq:(Medium) rs1217272526 Functional Loss SNV dbSNP153 33..33 33 - - - 91248 RMVar_ID_91248 Human_SNP_ID_89172613 m1A Human chr2 - 119681643 119681643 119681643 GGGTGTATACAGCTTCTCCCCGTCTTTGCCCAAGAGACTGCGCAGGGCCAGGTTGCCCGACAGAA GGGTGTATACAGCTTCTCCCCGTCTTTGCCCAGGAGACTGCGCAGGGCCAGGTTGCCCGACAGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:119681524..119681674 32194978 MeRIP-seq:(Medium) rs770039083 Functional Loss SNV dbSNP153 33..33 33 - - - 91249 RMVar_ID_91249 Human_SNP_ID_89207372 m1A Human chr2 - 119830820 119830820 119830820 GGAGGCCTCAGGAAACTTACAATCATAGTGGAAGGCAAAGAGAGAGCAAGGTGTCTCATGTGGCA GGAGGCCTCAGGAAACTTACAATCATAGTGGATGGCAAAGAGAGAGCAAGGTGTCTCATGTGGCA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:119830692..119830819 26863196 MeRIP-seq:(Medium) rs1279626079 Functional Loss SNV dbSNP153 33..33 33 - - - 91250 RMVar_ID_91250 Human_SNP_ID_197408562 m1A Human chr4 + 105146652 105146652 105146652 GGAGCGGGAGGAGGCCGGGGCGGAGCAGGAGGAGGCCCGGGCGGAGGAGGAGAGCCGGCGGTAGC GGAGCGGGAGGAGGCCGGGGCGGAGCAGGAGGCGGCCCGGGCGGAGGAGGAGAGCCGGCGGTAGC A C TET2 Ensembl:ENSG00000168769 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:105146499..105146824 26863196 MeRIP-seq:(Medium) rs1195649375 Functional Loss SNV dbSNP153 33..33 33 - - - 91251 RMVar_ID_91251 Human_SNP_ID_197436891 m1A Human chr4 - 105263856 105263856 105263856 TCCATCCATCTCCCTCTTTCACTTTTCCTACTACATTTCTTCTACTCCCTCCCCCAGTTCTTACT TCCATCCATCTCCCTCTTTCACTTTTCCTACTGCATTTCTTCTACTCCCTCCCCCAGTTCTTACT T C TET2-AS1,TET2-AS1:2 RNACentral:URS00007E443A,RNACentral:URS0000D5DAB0 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:105263819..105263903 26863196 MeRIP-seq:(Medium) rs1448474525 Functional Loss SNV dbSNP153 33..33 33 - - - 91252 RMVar_ID_91252 Human_SNP_ID_197484958 m1A Human chr4 + 105456741 105456741 105456741 TCATGAAAGGGGGAAATGTAGTGACCAGTTACATTCTCTGCAAAGACACAAACAAACAAAACAAA TCATGAAAGGGGGAAATGTAGTGACCAGTTACGTTCTCTGCAAAGACACAAACAAACAAAACAAA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:105456701..105456817 26863410 MeRIP-seq:(Medium) rs754256853 Functional Loss SNV dbSNP153 33..33 33 - - - 91253 RMVar_ID_91253 Human_SNP_ID_197489166 m1A Human chr4 + 105473993 105473993 105473993 ACGGCGCGACCCGGTCCCTGCACTGGTCCCCAACCGCAGGCACGCAGCGGCTGGGGCACCCGTGC ACGGCGCGACCCGGTCCCTGCACTGGTCCCCAGCCGCAGGCACGCAGCGGCTGGGGCACCCGTGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:105473876..105474081 26863410 MeRIP-seq:(Medium) rs748041656 Functional Loss SNV dbSNP153 33..33 33 - - - 91254 RMVar_ID_91254 Human_SNP_ID_197489194 m1A Human chr4 + 105474028 105474021 105474029 GCAGGCACGCAGCGGCTGGGGCACCCGTGCGCAGCAGCCGCAGCAGCGCGCTCATGGCGTCAATG GCAGGCACGCAGCGGCTGGGGCACCC________CAGCCGCAGCAGCGCGCTCATGGCGTCAATG CGTGCGCAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:105473838..105474075 26863196 MeRIP-seq:(Medium) rs1553930854 Functional Loss DEL dbSNP153 27..34 33 - - - 91255 RMVar_ID_91255 Human_SNP_ID_197489206 m1A Human chr4 + 105474028 105474027 105474029 GCAGGCACGCAGCGGCTGGGGCACCCGTGCGCAGCAGCCGCAGCAGCGCGCTCATGGCGTCAATG GCAGGCACGCAGCGGCTGGGGCACCCGTGCGC__CAGCCGCAGCAGCGCGCTCATGGCGTCAATG CAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:105473838..105474075 26863196 MeRIP-seq:(Medium) rs1553930862 Functional Loss DEL dbSNP153 33..34 33 - - - 91256 RMVar_ID_91256 Human_SNP_ID_197489207 m1A Human chr4 + 105474028 105474028 105474028 GCAGGCACGCAGCGGCTGGGGCACCCGTGCGCAGCAGCCGCAGCAGCGCGCTCATGGCGTCAATG GCAGGCACGCAGCGGCTGGGGCACCCGTGCGCCGCAGCCGCAGCAGCGCGCTCATGGCGTCAATG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:105473838..105474075 26863196 MeRIP-seq:(Medium) rs754626127 Functional Loss SNV dbSNP153 33..33 33 - - - 91257 RMVar_ID_91257 Human_SNP_ID_197545548 m1A Human chr4 - 105700016 105700011 105700017 GTCTTCTAGATTACTTTCTCTTTTTTTCCTTCAGGCGTTTGCAATGGCTGCTACTGTGAACTTGG GTCTTCTAGATTACTTTCTCTTTTTTTCCTT______TTTGCAATGGCTGCTACTGTGAACTTGG ACGCCTG A INTS12 Ensembl:ENSG00000138785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:105699967..105702937 26863196 MeRIP-seq:(Medium) rs1459989968 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_25774827 91258 RMVar_ID_91258 Human_SNP_ID_197545554 m1A Human chr4 - 105700016 105700016 105700016 GTCTTCTAGATTACTTTCTCTTTTTTTCCTTCAGGCGTTTGCAATGGCTGCTACTGTGAACTTGG GTCTTCTAGATTACTTTCTCTTTTTTTCCTTCGGGCGTTTGCAATGGCTGCTACTGTGAACTTGG T C INTS12 Ensembl:ENSG00000138785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:105699967..105702937 26863196 MeRIP-seq:(Medium) rs1326237681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25774827 91259 RMVar_ID_91259 Human_SNP_ID_197590314 m1A Human chr4 + 105894512 105894512 105894512 CAAGGAGGCCATGGACTGGAGGAAGAGAAATGAGGACATTGAGAGGTACGGGAGATGACAGATGA CAAGGAGGCCATGGACTGGAGGAAGAGAAATGGGGACATTGAGAGGTACGGGAGATGACAGATGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:105894461..105894550 26863196 MeRIP-seq:(Medium) rs1317877924 Functional Loss SNV dbSNP153 33..33 33 - - - 91260 RMVar_ID_91260 Human_SNP_ID_197590602 m1A Human chr4 + 105895530 105895530 105895530 CCTCGCCGCTGTCCTCCGGGAGCGGCAGCAGTAGCCCGGGCGGCGAGGGCTGGGGGTTCCTCGAG CCTCGCCGCTGTCCTCCGGGAGCGGCAGCAGTGGCCCGGGCGGCGAGGGCTGGGGGTTCCTCGAG A G NPNT Ensembl:ENSG00000168743 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:105895488..105895660 26863196 MeRIP-seq:(Medium) rs938469085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795577 RMVar_hsa_circ_227828,RMVar_hsa_circ_87780 91261 RMVar_ID_91261 Human_SNP_ID_197590603 m1A Human chr4 + 105895530 105895530 105895530 CCTCGCCGCTGTCCTCCGGGAGCGGCAGCAGTAGCCCGGGCGGCGAGGGCTGGGGGTTCCTCGAG CCTCGCCGCTGTCCTCCGGGAGCGGCAGCAGTTGCCCGGGCGGCGAGGGCTGGGGGTTCCTCGAG A T NPNT Ensembl:ENSG00000168743 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:105895488..105895660 26863196 MeRIP-seq:(Medium) rs938469085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795577 RMVar_hsa_circ_227828,RMVar_hsa_circ_87780 91262 RMVar_ID_91262 Human_SNP_ID_197590619 m1A Human chr4 + 105895569 105895569 105895569 GCGGCGAGGGCTGGGGGTTCCTCGAGACTCTCAGAGGGGCGCCTCCCATCGGCGCCCACCACCCC GCGGCGAGGGCTGGGGGTTCCTCGAGACTCTCGGAGGGGCGCCTCCCATCGGCGCCCACCACCCC A G NPNT Ensembl:ENSG00000168743 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:105895472..105895605 26863410 MeRIP-seq:(Medium) rs1042128559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795577 RMVar_hsa_circ_227828,RMVar_hsa_circ_87780 91263 RMVar_ID_91263 Human_SNP_ID_197590638 m1A Human chr4 - 105895628 105895628 105895628 AAATCCATGTTGGGCAGCGGGTCCTGGGGCGCAGCGCAGTGGCGCGCGAGGAACAGGTTGGGGTG AAATCCATGTTGGGCAGCGGGTCCTGGGGCGCGGCGCAGTGGCGCGCGAGGAACAGGTTGGGGTG T C INTS12 Ensembl:ENSG00000138785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:105895519..105895648 26863196 MeRIP-seq:(Medium) rs1344087660 Functional Loss SNV dbSNP153 33..33 33 - - - 91264 RMVar_ID_91264 Human_SNP_ID_197689869 m1A Human chr4 - 106316191 106316191 106316191 GCTGAGGGGAGGGTAGAGGGTGAAAAGCTCGGATCTGTGTTTGGGGAAGGCCAGGCTTGCGCTCC GCTGAGGGGAGGGTAGAGGGTGAAAAGCTCGGCTCTGTGTTTGGGGAAGGCCAGGCTTGCGCTCC T G TBCK Ensembl:ENSG00000145348 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:106315999..106316216 26863196 MeRIP-seq:(Medium) rs1476257083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5531722,Human_RBP_ID_18424620,Human_RBP_ID_24029441 RMVar_hsa_circ_79207,RMVar_hsa_circ_227884 91265 RMVar_ID_91265 Human_SNP_ID_198002397 m1A Human chr4 + 107614384 107614384 107614384 ATTCGTGTTCCTGAAATAAATTCAAAGTCTTCATGGCTAAAGGAGAGGAAAAAAAGAAAATTATT ATTCGTGTTCCTGAAATAAATTCAAAGTCTTCGTGGCTAAAGGAGAGGAAAAAAAGAAAATTATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:107614238..107631631 32194978 MeRIP-seq:(Medium) rs768649817 Functional Loss SNV dbSNP153 33..33 33 - - - 91266 RMVar_ID_91266 Human_SNP_ID_198011965 m1A Human chr4 + 107654806 107654806 107654806 GGATTGCGAAGAATGGCCACACGGCGGCCCTCATACATCAGAGCAAATGCTGTACAGCCGTCCAG GGATTGCGAAGAATGGCCACACGGCGGCCCTCCTACATCAGAGCAAATGCTGTACAGCCGTCCAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:107654755..107656950 32194978 MeRIP-seq:(Medium) rs778694415 Functional Loss SNV dbSNP153 33..33 33 - - - 91267 RMVar_ID_91267 Human_SNP_ID_198020032 m1A Human chr4 + 107687145 107687145 107687145 TCAACAAATACTTCAAAAAACGGTAAACTTGCACCTTCATGAATTTGCCTTGCATTGTTGCGATC TCAACAAATACTTCAAAAAACGGTAAACTTGCCCCTTCATGAATTTGCCTTGCATTGTTGCGATC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:107687094..107693787 32194978 MeRIP-seq:(Medium) rs770769015 Functional Loss SNV dbSNP153 33..33 33 - - - 91268 RMVar_ID_91268 Human_SNP_ID_198027163 m1A Human chr4 + 107717713 107717713 107717713 CCTGGCACACACTAAACTCTCCTTTGTGTTTAACTAATATCACCCTTACCCCCGTGCCCAACCTA CCTGGCACACACTAAACTCTCCTTTGTGTTTAGCTAATATCACCCTTACCCCCGTGCCCAACCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:107717711..107717888 26863196 MeRIP-seq:(Medium) rs995276548 Functional Loss SNV dbSNP153 33..33 33 - - - 91269 RMVar_ID_91269 Human_SNP_ID_198089553 m1A Human chr4 + 107989928 107989926 107989928 GCCCGGGTCTCCTCGCTGTCGCCGCCGCTGCCACACCATGGCCTTCGTCACCAGGCAGTTCATGC GCCCGGGTCTCCTCGCTGTCGCCGCCGCTGC__CACCATGGCCTTCGTCACCAGGCAGTTCATGC CCA C HADH Ensembl:ENSG00000138796 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:107989826..107990050 26863410 MeRIP-seq:(Medium) rs749063053 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4795085 91270 RMVar_ID_91270 Human_SNP_ID_198089571 m1A Human chr4 - 107989967 107989967 107989967 TGGCCGAGGCCGAGGCGGTGGACGAGGAGGACACGGAACGCATGAACTGCCTGGTGACGAAGGCC TGGCCGAGGCCGAGGCGGTGGACGAGGAGGACTCGGAACGCATGAACTGCCTGGTGACGAAGGCC T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:107989877..107989972 26863410 MeRIP-seq:(Medium) rs761268836 Functional Loss SNV dbSNP153 33..33 33 - - - 91271 RMVar_ID_91271 Human_SNP_ID_198094128 m1A Human chr4 - 108009761 108009761 108009761 ACCAACACTACTGTGTGACCAGTTGCTGCAGCAACCTAGAGCAACAAAAGAACAATTTCTTTTTA ACCAACACTACTGTGTGACCAGTTGCTGCAGCGACCTAGAGCAACAAAAGAACAATTTCTTTTTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:108009751..108009775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 91272 RMVar_ID_91272 Human_SNP_ID_198239906 m1A Human chr4 + 108620599 108620599 108620599 TTTTTTCTTCCTCTTCCGGGGACGTTGTCTGCAGGTATGGATGTTGTTCTCTTTTCCCTGTCTTT TTTTTTCTTCCTCTTCCGGGGACGTTGTCTGCGGGTATGGATGTTGTTCTCTTTTCCCTGTCTTT A G RPL34 Ensembl:ENSG00000109475 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr4:108620576..108620742;chr4:108620576..108620625;chr4:108620565..108620716 26863196,32194978 MeRIP-seq:(Medium) rs1044052339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249331,Human_RBP_ID_786981,Human_RBP_ID_4795088,Human_RBP_ID_17661693,Human_RBP_ID_18195029,Human_RBP_ID_22457738,Human_RBP_ID_22679969,Human_RBP_ID_23213852,Human_RBP_ID_24030029,Human_RBP_ID_26825562 Human_Splice_Rec_591177,Human_Splice_Rec_591185 91273 RMVar_ID_91273 Human_SNP_ID_198239907 m1A Human chr4 + 108620599 108620599 108620599 TTTTTTCTTCCTCTTCCGGGGACGTTGTCTGCAGGTATGGATGTTGTTCTCTTTTCCCTGTCTTT TTTTTTCTTCCTCTTCCGGGGACGTTGTCTGCTGGTATGGATGTTGTTCTCTTTTCCCTGTCTTT A T RPL34 Ensembl:ENSG00000109475 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr4:108620576..108620742;chr4:108620576..108620625;chr4:108620565..108620716 26863196,32194978 MeRIP-seq:(Medium) rs1044052339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249331,Human_RBP_ID_786981,Human_RBP_ID_4795088,Human_RBP_ID_17661693,Human_RBP_ID_18195029,Human_RBP_ID_22457738,Human_RBP_ID_22679969,Human_RBP_ID_23213852,Human_RBP_ID_24030029,Human_RBP_ID_26825562 Human_Splice_Rec_591177,Human_Splice_Rec_591185 91274 RMVar_ID_91274 Human_SNP_ID_198240289 m1A Human chr4 + 108621928 108621928 108621928 GATTTTATTTACTTTTACAATGGAAAGATTTGATGTTACTCTATTCTTAATTTAGGCACTCAGAA GATTTTATTTACTTTTACAATGGAAAGATTTGTTGTTACTCTATTCTTAATTTAGGCACTCAGAA A T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:108621926..108622100;chr4:108621926..108622096 26863196 MeRIP-seq:(Medium) rs753442141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021230,Human_RBP_ID_22679346 Human_Splice_Rec_591179,Human_Splice_Rec_591187,Human_Splice_Rec_591197,Human_Splice_Rec_591203,Human_Splice_Rec_591209,Human_Splice_Rec_591217 91275 RMVar_ID_91275 Human_SNP_ID_198240377 m1A Human chr4 + 108622193 108622193 108622193 CACCAAAATCTGCATGTGGTGTGTGCCCAGGCAGACTTCGAGGGGTAAGTGTACCTTTTACTGTG CACCAAAATCTGCATGTGGTGTGTGCCCAGGCCGACTTCGAGGGGTAAGTGTACCTTTTACTGTG A C RPL34 Ensembl:ENSG00000109475 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:108622008..108622243 26863196 MeRIP-seq:(Medium) rs771440307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249332,Human_RBP_ID_611186,Human_RBP_ID_786982,Human_RBP_ID_838193,Human_RBP_ID_1971655,Human_RBP_ID_9334765,Human_RBP_ID_17662121,Human_RBP_ID_18195033,Human_RBP_ID_22458412,Human_RBP_ID_23214042,Human_RBP_ID_24030040,Human_RBP_ID_26825576 Human_Splice_Rec_591180,Human_Splice_Rec_591181,Human_Splice_Rec_591188,Human_Splice_Rec_591189,Human_Splice_Rec_591198,Human_Splice_Rec_591199,Human_Splice_Rec_591204,Human_Splice_Rec_591210,Human_Splice_Rec_591211,Human_Splice_Rec_591218,Human_Splice_Rec_591219 Human_miRNA_ID_2455070 RMVar_hsa_circ_23435,RMVar_hsa_circ_372800,RMVar_hsa_circ_227920,RMVar_hsa_circ_356074 91276 RMVar_ID_91276 Human_SNP_ID_198240588 m1A Human chr4 - 108622869 108622869 108622869 ACTCCATCTATCTTTGTCCAAACCACTAACAGAGACTTTCTTACCCACCTCCTGAACAAAACCAA ACTCCATCTATCTTTGTCCAAACCACTAACAGCGACTTTCTTACCCACCTCCTGAACAAAACCAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:108622867..108623053 26863196 MeRIP-seq:(Medium) rs964983151 Functional Loss SNV dbSNP153 33..33 33 - - - 91277 RMVar_ID_91277 Human_SNP_ID_198249447 m1A Human chr4 - 108657498 108657498 108657498 TCCAGGATTATGAAACCTAAACCTCCCATTGTAAATAGGAAGCTGGATGCAAGTCCTTCCATAAT TCCAGGATTATGAAACCTAAACCTCCCATTGTGAATAGGAAGCTGGATGCAAGTCCTTCCATAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:108655572..108657560 32194978 MeRIP-seq:(Medium) rs748553856 Functional Loss SNV dbSNP153 33..33 33 - - - 91278 RMVar_ID_91278 Human_SNP_ID_198275867 m1A Human chr4 + 108762955 108762955 108762955 AAGGTGCAAGGTGCAAGGTCTGCGCGCCTCCTACGCGAGCCTGGGACTGCCTTGGCGGCCCCGGC AAGGTGCAAGGTGCAAGGTCTGCGCGCCTCCTTCGCGAGCCTGGGACTGCCTTGGCGGCCCCGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:108762908..108763060 26863196 MeRIP-seq:(Medium) rs1267801279 Functional Loss SNV dbSNP153 33..33 33 - - - 91279 RMVar_ID_91279 Human_SNP_ID_198431966 m1A Human chr4 + 109435908 109435908 109435908 ACAGGTTGGGGTGGGAGGGAAAGGTTGACTCTAGGCAGAGGTTACAGCATGAACTAAAGTTTGGA ACAGGTTGGGGTGGGAGGGAAAGGTTGACTCTCGGCAGAGGTTACAGCATGAACTAAAGTTTGGA A C SEC24B Ensembl:ENSG00000138802 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:109435906..109436069 26863196 MeRIP-seq:(Medium) rs910218578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837384 RMVar_hsa_circ_88963,RMVar_hsa_circ_121412,RMVar_hsa_circ_227935,RMVar_hsa_circ_227936 91280 RMVar_ID_91280 Human_SNP_ID_198458897 m1A Human chr4 - 109542975 109542975 109542975 CATTATCTAAACTTCTCCCAAATCTCAATTCCAAGCTTTTCATATCCTAACCACTACATTTTATC CATTATCTAAACTTCTCCCAAATCTCAATTCCGAGCTTTTCATATCCTAACCACTACATTTTATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:109542928..109543126 26863196 MeRIP-seq:(Medium) rs1336821580 Functional Loss SNV dbSNP153 33..33 33 - - - 91281 RMVar_ID_91281 Human_SNP_ID_198463237 m1A Human chr4 + 109560293 109560293 109560293 CAGGCGCTGACGAGGAGCCCGGCTGAGGGAGGATGCGCCGCTGACGCCTGCGGGAGCCGCGCGCC CAGGCGCTGACGAGGAGCCCGGCTGAGGGAGGGTGCGCCGCTGACGCCTGCGGGAGCCGCGCGCC A G MCUB Ensembl:ENSG00000005059 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:109560242..109560697 26863196 MeRIP-seq:(Medium) rs1427517807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611361,Human_RBP_ID_18817123 91282 RMVar_ID_91282 Human_SNP_ID_198463283 m1A Human chr4 + 109560403 109560403 109560403 CGGCTGCTGCCGACCCCTGGCACCTGGCGCCCAGCGCGCCCGTGGCCGCTGCCGCCTCCGCCCCA CGGCTGCTGCCGACCCCTGGCACCTGGCGCCCGGCGCGCCCGTGGCCGCTGCCGCCTCCGCCCCA A G MCUB Ensembl:ENSG00000005059 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:109560353..109648521 32194978 MeRIP-seq:(Medium) rs970609186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4770022 Human_Splice_Rec_592079,Human_Splice_Rec_592087,Human_Splice_Rec_592091 91283 RMVar_ID_91283 Human_SNP_ID_198493266 m1A Human chr4 + 109682739 109682739 109682739 GACCACCTGAAGGAACAGCTGCAGCCCCTTGAACAGGTTAGGAAGCATCACGGTTGAGTATATTT GACCACCTGAAGGAACAGCTGCAGCCCCTTGAGCAGGTTAGGAAGCATCACGGTTGAGTATATTT A G MCUB Ensembl:ENSG00000005059 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:109682659..109682759 32194978 MeRIP-seq:(Medium) rs1040220502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_592099 RMVar_hsa_circ_102522,RMVar_hsa_circ_84687,RMVar_hsa_circ_227992,RMVar_hsa_circ_227993 91284 RMVar_ID_91284 Human_SNP_ID_198497222 m1A Human chr4 - 109697766 109697765 109697767 AGTGATTGTTTTTCAACTTTTCATTAACAGAGAAATGTTTGATCCGGCAGAAAAGTACAAAATGG AGTGATTGTTTTTCAACTTTTCATTAACAGA__AATGTTTGATCCGGCAGAAAAGTACAAAATGG TTC T CASP6 Ensembl:ENSG00000138794 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:109697694..109702728 26863196 MeRIP-seq:(Medium) rs751651515 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15024302,Human_RBP_ID_26350228 Human_Splice_Rec_592124,Human_Splice_Rec_592156,Human_Splice_Rec_592164 RMVar_hsa_circ_11868,RMVar_hsa_circ_349062,RMVar_hsa_circ_329369,RMVar_hsa_circ_227995,RMVar_hsa_circ_359963 91285 RMVar_ID_91285 Human_SNP_ID_198497223 m1A Human chr4 - 109697766 109697766 109697766 AGTGATTGTTTTTCAACTTTTCATTAACAGAGAAATGTTTGATCCGGCAGAAAAGTACAAAATGG AGTGATTGTTTTTCAACTTTTCATTAACAGAGGAATGTTTGATCCGGCAGAAAAGTACAAAATGG T C CASP6 Ensembl:ENSG00000138794 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:109697694..109702728 26863196 MeRIP-seq:(Medium) rs1313795054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15024302,Human_RBP_ID_26350228 Human_Splice_Rec_592124,Human_Splice_Rec_592156,Human_Splice_Rec_592164 RMVar_hsa_circ_11868,RMVar_hsa_circ_349062,RMVar_hsa_circ_329369,RMVar_hsa_circ_227995,RMVar_hsa_circ_359963 91286 RMVar_ID_91286 Human_SNP_ID_198505190 m1A Human chr4 + 109729751 109729751 109729751 AGTCGGTGGTCTGGGCCTGCTCCTGGCACCTGACAACAGCGGCCATGAGGAGGAGCAGGAGGGTG AGTCGGTGGTCTGGGCCTGCTCCTGGCACCTGCCAACAGCGGCCATGAGGAGGAGCAGGAGGGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:109729701..109729977 32194978 MeRIP-seq:(Medium) rs1414519891 Functional Loss SNV dbSNP153 33..33 33 - - - 91287 RMVar_ID_91287 Human_SNP_ID_198505294 m1A Human chr4 - 109729966 109729966 109729966 CGCTGCCTGCCCGAGGCGGTTCACGTAAAGACAGCGAGATCCTGAGGGCCAGCCGGGAAGGAGGC CGCTGCCTGCCCGAGGCGGTTCACGTAAAGACGGCGAGATCCTGAGGGCCAGCCGGGAAGGAGGC T C PLA2G12A,AC126283.2 Ensembl:ENSG00000123739,Ensembl:ENSG00000285330 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:109729947..109730034 26863410 MeRIP-seq:(Medium) rs1302267629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838198,Human_RBP_ID_4795093,Human_RBP_ID_5150764,Human_RBP_ID_8943761 Human_miRNA_ID_2426568 RMVar_hsa_circ_120570,RMVar_hsa_circ_227998 91288 RMVar_ID_91288 Human_SNP_ID_198527871 m1A Human chr4 + 109816203 109816203 109816203 TTTCGAGGCGGAGGTCGTGGAGGCTTTAATCGAGGTGGTGGAGGTGGCGGCTTCAACCGAGGTGG TTTCGAGGCGGAGGTCGTGGAGGCTTTAATCGCGGTGGTGGAGGTGGCGGCTTCAACCGAGGTGG A C GAR1 Ensembl:ENSG00000109534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:109816122..109816410;chr4:109816098..109816445 26863196 MeRIP-seq:(Medium) rs147947279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611501,Human_RBP_ID_4770170,Human_RBP_ID_7257326,Human_RBP_ID_8582463,Human_RBP_ID_22457745,Human_RBP_ID_26349504 Human_Splice_Rec_592342,Human_Splice_Rec_592350,Human_Splice_Rec_592362 91289 RMVar_ID_91289 Human_SNP_ID_198527872 m1A Human chr4 + 109816203 109816203 109816203 TTTCGAGGCGGAGGTCGTGGAGGCTTTAATCGAGGTGGTGGAGGTGGCGGCTTCAACCGAGGTGG TTTCGAGGCGGAGGTCGTGGAGGCTTTAATCGGGGTGGTGGAGGTGGCGGCTTCAACCGAGGTGG A G GAR1 Ensembl:ENSG00000109534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:109816122..109816410;chr4:109816098..109816445 26863196 MeRIP-seq:(Medium) rs147947279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611501,Human_RBP_ID_4770170,Human_RBP_ID_7257326,Human_RBP_ID_8582463,Human_RBP_ID_22457745,Human_RBP_ID_26349504 Human_Splice_Rec_592342,Human_Splice_Rec_592350,Human_Splice_Rec_592362 91290 RMVar_ID_91290 Human_SNP_ID_198529482 m1A Human chr4 - 109822427 109822427 109822427 CCTCTTCCTCCTCCTCGGCCTCCCCTGCCACCACCTCTTGGAGGTCCTTTCTCACCTGGAGGTCG CCTCTTCCTCCTCCTCGGCCTCCCCTGCCACCGCCTCTTGGAGGTCCTTTCTCACCTGGAGGTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:109822376..109824441 26863196 MeRIP-seq:(Medium) rs1310808032 Functional Loss SNV dbSNP153 33..33 33 - - - 91291 RMVar_ID_91291 Human_SNP_ID_198584785 m1A Human chr4 - 110051280 110051280 110051280 GCTCAGGGTCATCAAGAAAAATAATAGACAAAAGAAAATGGCACAAGGAATCACACGTGGTGCAG GCTCAGGGTCATCAAGAAAAATAATAGACAAATGAAAATGGCACAAGGAATCACACGTGGTGCAG T A ELOVL6 Ensembl:ENSG00000170522 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:110051241..110051343 26863196 MeRIP-seq:(Medium) rs1349099503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115928,RMVar_hsa_circ_228001 91292 RMVar_ID_91292 Human_SNP_ID_198584787 m1A Human chr4 - 110051287 110051287 110051287 AGCCATAGCTCAGGGTCATCAAGAAAAATAATAGACAAAAGAAAATGGCACAAGGAATCACACGT AGCCATAGCTCAGGGTCATCAAGAAAAATAATGGACAAAAGAAAATGGCACAAGGAATCACACGT T C ELOVL6 Ensembl:ENSG00000170522 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:110051241..110051343 26863196 MeRIP-seq:(Medium) rs773300923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115928,RMVar_hsa_circ_228001 91293 RMVar_ID_91293 Human_SNP_ID_198621423 m1A Human chr4 - 110198449 110198441 110198449 GAGACGACCGCTGGAGACCGAGCGGCGTGGGGAAGACCTAGGGGGGTGGGTGGGGGAAGCAGACA GAGACGACCGCTGGAGACCGAGCGGCGTGGGG________GGGGGGTGGGTGGGGGAAGCAGACA CTAGGTCTT C ELOVL6 Ensembl:ENSG00000170522 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:110198398..110198566 26863196 MeRIP-seq:(Medium) rs1374228506 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_5121289,Human_RBP_ID_7257676,Human_RBP_ID_9435836,Human_RBP_ID_23034925,Human_RBP_ID_24547888,Human_RBP_ID_26350232 91294 RMVar_ID_91294 Human_SNP_ID_198621453 m1A Human chr4 - 110198523 110198523 110198523 GCCCCAGAGAGAGGAGCTGGGAGCGGAGGCGCAGGCAATGCTCAGCCCTGGATGTAGCTGAGAGG GCCCCAGAGAGAGGAGCTGGGAGCGGAGGCGCTGGCAATGCTCAGCCCTGGATGTAGCTGAGAGG T A ELOVL6 Ensembl:ENSG00000170522 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:110198287..110198617 26863196 MeRIP-seq:(Medium) rs1410860503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786697,Human_RBP_ID_4794685,Human_RBP_ID_18424622,Human_RBP_ID_23034870 91295 RMVar_ID_91295 Human_SNP_ID_198727216 m1A Human chr4 - 110618487 110618487 110618487 CCTCCCTATCCACCAAGAGCTTCCCCTTCTTCAACTCTATGAACGTCAACCCCCTGTCATCACAG CCTCCCTATCCACCAAGAGCTTCCCCTTCTTCGACTCTATGAACGTCAACCCCCTGTCATCACAG T C PITX2 Ensembl:ENSG00000164093 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:110618437..110618601 26863196 MeRIP-seq:(Medium) rs751484586 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_11821,GWAS_ID_11822,GWAS_ID_11823 91296 RMVar_ID_91296 Human_SNP_ID_198727990 m1A Human chr4 + 110621084 110621084 110621084 CACCGGCGCCCTCCCAGGCGGCGCTGCCTTCCACATTCTCTCCTGGTCTACTTGGCCTGTACCTC CACCGGCGCCCTCCCAGGCGGCGCTGCCTTCCGCATTCTCTCCTGGTCTACTTGGCCTGTACCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:110621064..110621132 26863196 MeRIP-seq:(Medium) rs1017259920 Functional Loss SNV dbSNP153 33..33 33 - - - 91297 RMVar_ID_91297 Human_SNP_ID_199094332 m1A Human chr4 + 112145720 112145720 112145720 GGCGAGCCCGCGGCGGCGCGGACAGCGGCCGAAGGAGAGCGAGCAGGTGAGCGCGGGGAGGGGCG GGCGAGCCCGCGGCGGCGCGGACAGCGGCCGAGGGAGAGCGAGCAGGTGAGCGCGGGGAGGGGCG A G FAM241A Ensembl:ENSG00000174749 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:112145618..112145744 26863196 MeRIP-seq:(Medium) rs1308694264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5242134,Human_RBP_ID_5326039,Human_RBP_ID_22745806,Human_RBP_ID_23034926,Human_RBP_ID_26791658,Human_RBP_ID_27825015,Human_RBP_ID_27841864 Human_Splice_Rec_592875 91298 RMVar_ID_91298 Human_SNP_ID_199102702 m1A Human chr4 - 112180615 112180613 112180616 AAATTTAGAAACTTTTATAGCAATTTTATACCACATCATTTTTACTATATTTTACAAATGTATCA AAATTTAGAAACTTTTATAGCAATTTTATAC___ATCATTTTTACTATATTTTACAAATGTATCA TGTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:112180613..112180732 26863196 MeRIP-seq:(Medium) rs1385526429 Functional Loss DEL dbSNP153 32..34 33 - - - 91299 RMVar_ID_91299 Human_SNP_ID_199115658 m1A Human chr4 + 112231835 112231835 112231835 GAGCTGAGGCGAGAAGGGCCATGCGGACGGCGAGGGAGTCCAGAGCCTTGAGCCCGGTGCTCCTC GAGCTGAGGCGAGAAGGGCCATGCGGACGGCGGGGGAGTCCAGAGCCTTGAGCCCGGTGCTCCTC A G AP1AR Ensembl:ENSG00000138660 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:112231786..112231937;chr4:112231786..112231953 26863196 MeRIP-seq:(Medium) rs1379049701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4770385,Human_RBP_ID_7258076 91300 RMVar_ID_91300 Human_SNP_ID_199115739 m1A Human chr4 - 112232079 112232079 112232079 GTCCAGCAGCAGTTCCCCATCGCATGCCGCCCAGGCGCCGCCGCTCCTCCTCCTCCTCCCGCTCA GTCCAGCAGCAGTTCCCCATCGCATGCCGCCCGGGCGCCGCCGCTCCTCCTCCTCCTCCCGCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:112232035..112254754 26863196 MeRIP-seq:(Medium) rs536571351 Functional Loss SNV dbSNP153 33..33 33 - - - 91301 RMVar_ID_91301 Human_SNP_ID_199115775 m1A Human chr4 + 112232135 112232135 112232135 CTGCTGGACGCAGTGCTTCGGACTGCTTCGCAAGGAAGCGGGGCGGCTGCAGCGAGTAGGCGGCG CTGCTGGACGCAGTGCTTCGGACTGCTTCGCACGGAAGCGGGGCGGCTGCAGCGAGTAGGCGGCG A C AP1AR Ensembl:ENSG00000138660 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:112232085..112253269 26863196 MeRIP-seq:(Medium) rs1484788599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611666,Human_RBP_ID_4795597,Human_RBP_ID_23120141 Human_Splice_Rec_592877,Human_Splice_Rec_592889,Human_Splice_Rec_592907,Human_Splice_Rec_592911,Human_Splice_Rec_592927 91302 RMVar_ID_91302 Human_SNP_ID_199122696 m1A Human chr4 + 112263070 112263070 112263070 TGCACAGCGTGAAGCAGCCAGGGCAGCAAAGCAGCGAAAGCTCTTGGAGGTGAGGGGAAAAGACC TGCACAGCGTGAAGCAGCCAGGGCAGCAAAGCGGCGAAAGCTCTTGGAGGTGAGGGGAAAAGACC A G AP1AR Ensembl:ENSG00000138660 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:112263022..112265095 32194978 MeRIP-seq:(Medium) rs763234247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19121791 Human_Splice_Rec_592886,Human_Splice_Rec_592887,Human_Splice_Rec_592898,Human_Splice_Rec_592899 RMVar_hsa_circ_69916,RMVar_hsa_circ_311041,RMVar_hsa_circ_73936,RMVar_hsa_circ_59528,RMVar_hsa_circ_228006 91303 RMVar_ID_91303 Human_SNP_ID_199123874 m1A Human chr4 - 112268650 112268650 112268650 AAATGCTATAAAGACAAGACAAAGTAAATTTAATCAGTAACATGACAGGACCATTAAATTGGTCT AAATGCTATAAAGACAAGACAAAGTAAATTTAGTCAGTAACATGACAGGACCATTAAATTGGTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:112268599..112268700 32194978 MeRIP-seq:(Medium) rs1288086815 Functional Loss SNV dbSNP153 33..33 33 - - - 91304 RMVar_ID_91304 Human_SNP_ID_199127733 m1A Human chr4 + 112285725 112285725 112285725 GAGCGAGGGGAATCGAGGAGACTGGGCGCAGGATGGGGGTGGACACCCGGCCGCTGCTCCTCCGC GAGCGAGGGGAATCGAGGAGACTGGGCGCAGGCTGGGGGTGGACACCCGGCCGCTGCTCCTCCGC A C ALPK1 Ensembl:ENSG00000073331 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:112285646..112285793 26863196 MeRIP-seq:(Medium) rs2293112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_592937 GWAS_ID_11824,GWAS_ID_11825,GWAS_ID_11826,GWAS_ID_11827,GWAS_ID_11828,GWAS_ID_11829,GWAS_ID_11830,GWAS_ID_11831 91305 RMVar_ID_91305 Human_SNP_ID_199127739 m1A Human chr4 + 112285735 112285735 112285735 AATCGAGGAGACTGGGCGCAGGATGGGGGTGGACACCCGGCCGCTGCTCCTCCGCGCGGGTAAGT AATCGAGGAGACTGGGCGCAGGATGGGGGTGGCCACCCGGCCGCTGCTCCTCCGCGCGGGTAAGT A C ALPK1 Ensembl:ENSG00000073331 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:112285684..112285842 26863196 MeRIP-seq:(Medium) rs1195375036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_592937 91306 RMVar_ID_91306 Human_SNP_ID_199182558 m1A Human chr4 - 112515217 112515217 112515217 CCGCACGGCTGCTGGGTCTGGTACACGATTGCAAACGGCGCCCTTCCCGGGCGCGGGCCGTCTCC CCGCACGGCTGCTGGGTCTGGTACACGATTGCCAACGGCGCCCTTCCCGGGCGCGGGCCGTCTCC T G NEUROG2 Ensembl:ENSG00000178403 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:112515167..112515336 26863196 MeRIP-seq:(Medium) rs1399585778 Functional Loss SNV dbSNP153 33..33 33 - - - 91307 RMVar_ID_91307 Human_SNP_ID_199407685 m1A Human chr4 + 113457539 113457539 113457539 GATGTACATGAGGGTTTAGAATAATAGTGTGGATTGGTTTATTGCTTTTGGACAAAGCTGAAAGA GATGTACATGAGGGTTTAGAATAATAGTGTGGGTTGGTTTATTGCTTTTGGACAAAGCTGAAAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:113457356..113457556 32194978 MeRIP-seq:(Medium) rs1180200020 Functional Loss SNV dbSNP153 33..33 33 - - - 91308 RMVar_ID_91308 Human_SNP_ID_199411040 m1A Human chr4 - 113471612 113471612 113471612 ATGGCTCTGAGAAAGAGTTGGAAGAATGTAGAATGGCTAAAGATCTATGAGGAATAAAAAGAAAG ATGGCTCTGAGAAAGAGTTGGAAGAATGTAGACTGGCTAAAGATCTATGAGGAATAAAAAGAAAG T G CAMK2D Ensembl:ENSG00000145349 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:113471607..113471779 26863196 MeRIP-seq:(Medium) rs569776067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35347,RMVar_hsa_circ_14713,RMVar_hsa_circ_17473,RMVar_hsa_circ_74693 91309 RMVar_ID_91309 Human_SNP_ID_199425276 m1A Human chr4 + 113531256 113531256 113531256 CACATATCCACTGGCTTTCCATAAGGATCTTTACGTAAAACTTCTGGAGAAAGATATCCAGGTGT CACATATCCACTGGCTTTCCATAAGGATCTTTGCGTAAAACTTCTGGAGAAAGATATCCAGGTGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:113531215..113547705 32194978 MeRIP-seq:(Medium) rs557144643 Functional Loss SNV dbSNP153 33..33 33 - - - 91310 RMVar_ID_91310 Human_SNP_ID_199477025 m1A Human chr4 + 113761221 113761221 113761221 CGAAAGTAGCTCGCCCGCGAGGGAGTGTGCGCAGGGGCGGGGCGGGAGGGGAGATGACCAGAAAG CGAAAGTAGCTCGCCCGCGAGGGAGTGTGCGCCGGGGCGGGGCGGGAGGGGAGATGACCAGAAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:113761180..113761330 32194978 MeRIP-seq:(Medium) rs545705023 Functional Loss SNV dbSNP153 33..33 33 - - - 91311 RMVar_ID_91311 Human_SNP_ID_199477239 m1A Human chr4 + 113761757 113761757 113761757 GCGGCGAGAGAAAGAGCGCTCGGCTCAGGCGAAGCCTCTTCTGCCGTCCCCAGGCCTCCGTCTCC GCGGCGAGAGAAAGAGCGCTCGGCTCAGGCGAGGCCTCTTCTGCCGTCCCCAGGCCTCCGTCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:113761707..113761855 26863196 MeRIP-seq:(Medium) rs1439564675 Functional Loss SNV dbSNP153 33..33 33 - - - 91312 RMVar_ID_91312 Human_SNP_ID_199511105 m1A Human chr4 + 113902032 113902032 113902032 TGGAACTCAGGACTCACCACGTTTTCTAAAGGAGCAAGAGAAATAAACATCTCCACTCTCTCTAA TGGAACTCAGGACTCACCACGTTTTCTAAAGGCGCAAGAGAAATAAACATCTCCACTCTCTCTAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:113901981..113902082 32194978 MeRIP-seq:(Medium) rs1196607406 Functional Loss SNV dbSNP153 33..33 33 - - - 91313 RMVar_ID_91313 Human_SNP_ID_199511316 m1A Human chr4 - 113902582 113902582 113902582 TGTCAACTGGCAAAAGTGTATGGCTTTTCAACATCACAGCCGACCCATATGAGAGGGTGGACCTA TGTCAACTGGCAAAAGTGTATGGCTTTTCAACGTCACAGCCGACCCATATGAGAGGGTGGACCTA T C ARSJ Ensembl:ENSG00000180801 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:113902531..113902732 32194978 MeRIP-seq:(Medium) rs1562327150 Functional Loss SNV dbSNP153 33..33 33 - - - 91314 RMVar_ID_91314 Human_SNP_ID_199528805 m1A Human chr4 + 113978872 113978872 113978872 CAGGTCCCAGGTGAGACTCCACGCGGAGAACCACGCGCCCCGCGCCGCTGCGGGCGCACACATGC CAGGTCCCAGGTGAGACTCCACGCGGAGAACCGCGCGCCCCGCGCCGCTGCGGGCGCACACATGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:113978827..113979028 32194978 MeRIP-seq:(Medium) rs777909842 Functional Loss SNV dbSNP153 33..33 33 - - - 91315 RMVar_ID_91315 Human_SNP_ID_199677849 m1A Human chr4 - 114598850 114598850 114598850 AGGTGTCGCCGCCTTCGGTGGTTCGGGGGCGTAAGGGAGGCTTCGGAGTTAGCGTGTTGGCTAAG AGGTGTCGCCGCCTTCGGTGGTTCGGGGGCGTGAGGGAGGCTTCGGAGTTAGCGTGTTGGCTAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:114598799..114599018 26863196 MeRIP-seq:(Medium) rs532689388 Functional Loss SNV dbSNP153 33..33 33 - - - 91316 RMVar_ID_91316 Human_SNP_ID_199678109 m1A Human chr4 + 114599701 114599701 114599701 CTGTGCGGGCCCCCGGGATTAGAGAAGAGGTGAGCGCCTGCGGGCGGGGAGAGAAGGACGCGCTG CTGTGCGGGCCCCCGGGATTAGAGAAGAGGTGTGCGCCTGCGGGCGGGGAGAGAAGGACGCGCTG A T UGT8 Ensembl:ENSG00000174607 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:114599693..114599776 26863196 MeRIP-seq:(Medium) rs971969786 Functional Loss SNV dbSNP153 33..33 33 - - - 91317 RMVar_ID_91317 Human_SNP_ID_200610058 m1A Human chr4 + 118279679 118279672 118279679 ATGGGCGAAGTTTATTCAGCATCCGGCAATGGACTTATCGTAGTTGGGGAAACGGGTGTTCCGAA ATGGGCGAAGTTTATTCAGCATCCGG_______CTTATCGTAGTTGGGGAAACGGGTGTTCCGAA GCAATGGA G SNHG8 Ensembl:ENSG00000269893 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:118279628..118279774 32194978 MeRIP-seq:(Medium) rs1393004486 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_612007,Human_RBP_ID_1140004,Human_RBP_ID_1634401,Human_RBP_ID_1972094,Human_RBP_ID_3726870,Human_RBP_ID_5608120,Human_RBP_ID_7260869,Human_RBP_ID_8582963,Human_RBP_ID_9149602,Human_RBP_ID_15030104,Human_RBP_ID_18032463,Human_RBP_ID_24032052,Human_RBP_ID_26512919 Human_Splice_Rec_601130,Human_Splice_Rec_601134,Human_Splice_Rec_601140,Human_Splice_Rec_601148,Human_Splice_Rec_601150,Human_Splice_Rec_601156,Human_Splice_Rec_601158 RMVar_hsa_circ_103008,RMVar_hsa_circ_228196 91318 RMVar_ID_91318 Human_SNP_ID_200683079 m1A Human chr4 - 118591808 118591808 118591808 CCACTCTGACGAGAAGACTGCCCAGCTCCAGGAACCGTAGCGCCCCAGTGACGTAGCCGAACACC CCACTCTGACGAGAAGACTGCCCAGCTCCAGGCACCGTAGCGCCCCAGTGACGTAGCCGAACACC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr4:118591753..118591880;chr4:118591778..118591924 26863196 MeRIP-seq:(Medium) rs1337847887 Functional Loss SNV dbSNP153 33..33 33 - - - 91319 RMVar_ID_91319 Human_SNP_ID_200717356 m1A Human chr4 + 118731347 118731347 118731347 CCATATCTGTGTTGATATGTGCAAAAGATGGCACATTAAATATTCCTTGGATCAGTTCTGGTGGG CCATATCTGTGTTGATATGTGCAAAAGATGGCGCATTAAATATTCCTTGGATCAGTTCTGGTGGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:118731341..118731441 32194978 MeRIP-seq:(Medium) rs1560603203 Functional Loss SNV dbSNP153 33..33 33 - - - 91320 RMVar_ID_91320 Human_SNP_ID_200725539 m1A Human chr4 - 118768237 118768237 118768237 AGATGCAACAGGTGCAAGGCCTACATGTGCCCATTTATGCAGTTCATCGAAGGAGGAAGGAGATA AGATGCAACAGGTGCAAGGCCTACATGTGCCCGTTTATGCAGTTCATCGAAGGAGGAAGGAGATA T C SEC24D Ensembl:ENSG00000150961 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:118768188..118768289 32194978 MeRIP-seq:(Medium) rs201472807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3966358,Human_RBP_ID_9396630,Human_RBP_ID_17409335,Human_RBP_ID_19013918 Human_Splice_Rec_601442,Human_Splice_Rec_601443,Human_Splice_Rec_601505,Human_Splice_Rec_601554,Human_Splice_Rec_601555,Human_Splice_Rec_601596,Human_Splice_Rec_601597,Human_Splice_Rec_601642,Human_Splice_Rec_601643,Human_Splice_Rec_601651 Human_miRNA_ID_353482,Human_miRNA_ID_2234253,Human_miRNA_ID_3028409 RMVar_hsa_circ_2862,RMVar_hsa_circ_9238,RMVar_hsa_circ_84495,RMVar_hsa_circ_228235,RMVar_hsa_circ_5086,RMVar_hsa_circ_98946,RMVar_hsa_circ_27718,RMVar_hsa_circ_109125,RMVar_hsa_circ_228238,RMVar_hsa_circ_228239,RMVar_hsa_circ_34933,RMVar_hsa_circ_59076,RMVar_hsa_circ_328608,RMVar_hsa_circ_45030,RMVar_hsa_circ_6245,RMVar_hsa_circ_6912 91321 RMVar_ID_91321 Human_SNP_ID_200741324 m1A Human chr4 - 118836012 118836011 118836012 GCGGGAGAAGCGACCGCAGCGGGAGCCCGGCCACCGAGGGCTGCCGGCACTAGGCGCAGAGCCGC GCGGGAGAAGCGACCGCAGCGGGAGCCCGGCC_CCGAGGGCTGCCGGCACTAGGCGCAGAGCCGC GT G SEC24D Ensembl:ENSG00000150961 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:118835961..118836155 26863196 MeRIP-seq:(Medium) rs1428772673 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_837804,Human_RBP_ID_4794690,Human_RBP_ID_5475018,Human_RBP_ID_5507286,Human_RBP_ID_5531382,Human_RBP_ID_9304217,Human_RBP_ID_17409352,Human_RBP_ID_19013920,Human_RBP_ID_24547889 Human_Splice_Rec_601427,Human_Splice_Rec_601581 RMVar_hsa_circ_85164,RMVar_hsa_circ_228249 91322 RMVar_ID_91322 Human_SNP_ID_200741337 m1A Human chr4 - 118836054 118836054 118836054 GTGAGTCCAGGCTAAGGGGACGCCGGCCGGGGAAGAGGCGCGGCGGGAGAAGCGACCGCAGCGGG GTGAGTCCAGGCTAAGGGGACGCCGGCCGGGGTAGAGGCGCGGCGGGAGAAGCGACCGCAGCGGG T A SEC24D Ensembl:ENSG00000150961 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:118835937..118836063 26863196 MeRIP-seq:(Medium) rs1229828822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837804,Human_RBP_ID_4794690,Human_RBP_ID_5531382,Human_RBP_ID_9304217,Human_RBP_ID_17409352,Human_RBP_ID_19013920,Human_RBP_ID_24547889 RMVar_hsa_circ_85164,RMVar_hsa_circ_228249 91323 RMVar_ID_91323 Human_SNP_ID_200832528 m1A Human chr4 - 119212754 119212754 119212754 GCCCAGCCCCGCTTCACGCCGACACCCGCCAGACACACTGACTGCTGCCACAGTACCGAGGCTCA GCCCAGCCCCGCTTCACGCCGACACCCGCCAGGCACACTGACTGCTGCCACAGTACCGAGGCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:119212703..119212828 26863196 MeRIP-seq:(Medium) rs543500078 Functional Loss SNV dbSNP153 33..33 33 - - - 91324 RMVar_ID_91324 Human_SNP_ID_200851590 m1A Human chr4 - 119297618 119297608 119297618 AACCCTATCTCTATTAAAAAATACAAAAAAATACAAAAAAATTAGCTGGGCATGTTGGCATGCAC AACCCTATCTCTATTAAAAAATACAAAAAAAT__________TAGCTGGGCATGTTGGCATGCAC AATTTTTTTGT A C4orf3 Ensembl:ENSG00000164096 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:119297567..119297718 32194978 MeRIP-seq:(Medium) rs569357641 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_612152,Human_RBP_ID_9149679 91325 RMVar_ID_91325 Human_SNP_ID_200887699 m1A Human chr4 - 119454849 119454838 119454849 AGCAGCGGGTTACATCCCGCCCGGCCACCGGTAGGCAGCGTCCGCTCAAGCGCGCTCCTGGAAGA AGCAGCGGGTTACATCCCGCCCGGCCACCGGT___________GCTCAAGCGCGCTCCTGGAAGA CGGACGCTGCCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:119454803..119454948 26863196 MeRIP-seq:(Medium) rs1395674264 Functional Loss DEL dbSNP153 33..43 33 - - - 91326 RMVar_ID_91326 Human_SNP_ID_200902136 m1A Human chr4 - 119515584 119515584 119515584 TGGGAAATATGTATATGTGTGCACTGAGAGAGAGGGTTGGCAAGAATGGAAGTTATGGGAGTTTT TGGGAAATATGTATATGTGTGCACTGAGAGAGGGGGTTGGCAAGAATGGAAGTTATGGGAGTTTT T C PDE5A Ensembl:ENSG00000138735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:119515533..119515651 26863196 MeRIP-seq:(Medium) rs1053764650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7262103,Human_RBP_ID_24032825 RMVar_hsa_circ_53235,RMVar_hsa_circ_80646,RMVar_hsa_circ_228292,RMVar_hsa_circ_61808,RMVar_hsa_circ_228294,RMVar_hsa_circ_85663,RMVar_hsa_circ_103257,RMVar_hsa_circ_228296,RMVar_hsa_circ_228297 91327 RMVar_ID_91327 Human_SNP_ID_200926943 m1A Human chr4 - 119628653 119628653 119628653 GCGCGGTGCCAACCATGGAGCGGGCCGGCCCCAGCTTCGGGCAGCAGCGACAGCAGCAGCAGCCC GCGCGGTGCCAACCATGGAGCGGGCCGGCCCCGGCTTCGGGCAGCAGCGACAGCAGCAGCAGCCC T C PDE5A Ensembl:ENSG00000138735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:119628602..119628838;chr4:119628613..119628946 26863196 MeRIP-seq:(Medium) rs772347394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101872,RMVar_hsa_circ_228316 91328 RMVar_ID_91328 Human_SNP_ID_487813526 m1A Human chr12 + 14842 14842 14842 CCTAGGATTCCCAGTCGTCCTTGTCCTCGTCTACCTGTGGCTGCTGCGGTGGCGGCAGAGGAGGG CCTAGGATTCCCAGTCGTCCTTGTCCTCGTCTGCCTGTGGCTGCTGCGGTGGCGGCAGAGGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:14801..15153 26863196 MeRIP-seq:(Medium) rs781975545 Functional Loss SNV dbSNP153 33..33 33 - - - 91329 RMVar_ID_91329 Human_SNP_ID_487814172 m1A Human chr12 - 15961 15961 15961 CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGAAGCAG CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCGTGAAGGAGCGAAAGCTGGAGAAGAAGAAGCAG T C WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1383517265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1319493 91330 RMVar_ID_91330 Human_SNP_ID_487814775 m1A Human chr12 + 17063 17063 17063 GCAGAGGGGGCAATGCCGGGGCCCAGGTCGGCAATGTACATGAGGTCGTTGGCAATGCTGGGCAG GCAGAGGGGGCAATGCCGGGGCCCAGGTCGGCGATGTACATGAGGTCGTTGGCAATGCTGGGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:16861..17098 26863196 MeRIP-seq:(Medium) rs1555061269 Functional Loss SNV dbSNP153 33..33 33 - - - 91331 RMVar_ID_91331 Human_SNP_ID_487815281 m1A Human chr12 - 18149 18149 18149 GTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCACCTGCAGGAATATGGCTCCATCTTCACGGGCG GTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCGCCTGCAGGAATATGGCTCCATCTTCACGGGCG T C WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:18101..18184 26863196 MeRIP-seq:(Medium) rs781784246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583,Human_RBP_ID_429335,Human_RBP_ID_872084,Human_RBP_ID_5349095,Human_RBP_ID_9365990,Human_RBP_ID_18975211,Human_RBP_ID_26321060 Human_Splice_Rec_1319482 91332 RMVar_ID_91332 Human_SNP_ID_487815284 m1A Human chr12 - 18152 18152 18152 GGTGTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCACCTGCAGGAATATGGCTCCATCTTCACGG GGTGTTCTCCAGTGCCAAGTACCCTGCTCCAGGGCACCTGCAGGAATATGGCTCCATCTTCACGG T C WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:18103..18179 26863196 MeRIP-seq:(Medium) rs1430040240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583,Human_RBP_ID_429335,Human_RBP_ID_872084,Human_RBP_ID_5349095,Human_RBP_ID_9365990,Human_RBP_ID_18975211,Human_RBP_ID_26321060 Human_Splice_Rec_1319482 91333 RMVar_ID_91333 Human_SNP_ID_487817333 m1A Human chr12 - 23397 23397 23397 TATTGTAGTCAGGATGCGACAGGGGTGAGGCTACAGACAGGGGACTTGCAAGCAGGGAGGGCAGG TATTGTAGTCAGGATGCGACAGGGGTGAGGCTGCAGACAGGGGACTTGCAAGCAGGGAGGGCAGG T C WASH8P Ensembl:ENSG00000226210 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:23375..23458 26863196 MeRIP-seq:(Medium) rs375730853 Functional Loss SNV dbSNP153 33..33 33 - - - 91334 RMVar_ID_91334 Human_SNP_ID_487890229 m1A Human chr12 - 285631 285631 285631 GGTAGACTGGGTACAATGTGATGGTGGCTGTGATGAGTGGTTTCATCAAGTTTGTGTGGGTGTAT GGTAGACTGGGTACAATGTGATGGTGGCTGTGGTGAGTGGTTTCATCAAGTTTGTGTGGGTGTAT T C KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:285474..286137 32194978 MeRIP-seq:(Medium) rs79230839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810137,Human_RBP_ID_23557351,Human_RBP_ID_25015169 Human_Splice_Rec_1319974,Human_Splice_Rec_1319978 Human_miRNA_ID_706476,Human_miRNA_ID_713726,Human_miRNA_ID_1515582 91335 RMVar_ID_91335 Human_SNP_ID_487892064 m1A Human chr12 - 292873 292873 292873 GAACTTGTGAAAGAGAGCACTGAAAAGAAAAGAGAGAAAAAGGTGCTGGACATCCCCTCAAAGTA GAACTTGTGAAAGAGAGCACTGAAAAGAAAAGCGAGAAAAAGGTGCTGGACATCCCCTCAAAGTA T G KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:292823..293042 26863196 MeRIP-seq:(Medium) rs1565523355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36388,Human_RBP_ID_194707,Human_RBP_ID_1479507,Human_RBP_ID_24543345,Human_RBP_ID_26321062 RMVar_hsa_circ_29544,RMVar_hsa_circ_277817,RMVar_hsa_circ_343114,RMVar_hsa_circ_339765,RMVar_hsa_circ_268453,RMVar_hsa_circ_154142,RMVar_hsa_circ_154143 91336 RMVar_ID_91336 Human_SNP_ID_487892069 m1A Human chr12 - 292904 292904 292904 AAAGAAGGAGAAGGCTGCTGCAGCCAAAGTTGAACTTGTGAAAGAGAGCACTGAAAAGAAAAGAG AAAGAAGGAGAAGGCTGCTGCAGCCAAAGTTGCACTTGTGAAAGAGAGCACTGAAAAGAAAAGAG T G KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:292853..292984 26863196 MeRIP-seq:(Medium) rs1429849844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36388,Human_RBP_ID_194707,Human_RBP_ID_991862,Human_RBP_ID_1479507,Human_RBP_ID_4220494,Human_RBP_ID_18625679,Human_RBP_ID_23557700,Human_RBP_ID_24543345,Human_RBP_ID_24966731,Human_RBP_ID_26321063 Human_miRNA_ID_1522199 RMVar_hsa_circ_29544,RMVar_hsa_circ_277817,RMVar_hsa_circ_343114,RMVar_hsa_circ_339765,RMVar_hsa_circ_268453,RMVar_hsa_circ_154142,RMVar_hsa_circ_154143 91337 RMVar_ID_91337 Human_SNP_ID_487896815 m1A Human chr12 - 309893 309893 309893 GGCAAAAATAGGAGGAAAAAAGTAAAAGAACTAATAGAAAAAGAAAAAGAAAAGGATCTGGACCT GGCAAAAATAGGAGGAAAAAAGTAAAAGAACTGATAGAAAAAGAAAAAGAAAAGGATCTGGACCT T C KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:309843..309917 26863196 MeRIP-seq:(Medium) rs760148803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22903540,Human_RBP_ID_26321067 Human_Splice_Rec_1319964,Human_Splice_Rec_1319965,Human_Splice_Rec_1320002,Human_Splice_Rec_1320004 RMVar_hsa_circ_23998,RMVar_hsa_circ_29544,RMVar_hsa_circ_277817,RMVar_hsa_circ_343114,RMVar_hsa_circ_339765,RMVar_hsa_circ_268453,RMVar_hsa_circ_154142,RMVar_hsa_circ_154143,RMVar_hsa_circ_59039,RMVar_hsa_circ_65846,RMVar_hsa_circ_288041,RMVar_hsa_circ_39002,RMVar_hsa_circ_4169,RMVar_hsa_circ_22906,RMVar_hsa_circ_43014,RMVar_hsa_circ_154146,RMVar_hsa_circ_154147 91338 RMVar_ID_91338 Human_SNP_ID_487897105 m1A Human chr12 + 310973 310973 310973 TCCATGCCCGTGCTGCTGCTACCTGTGATTCCACTTGCGGCAGTGCTTCAAGACGCACAGGAATA TCCATGCCCGTGCTGCTGCTACCTGTGATTCCCCTTGCGGCAGTGCTTCAAGACGCACAGGAATA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:310876..311075 32194978 MeRIP-seq:(Medium) rs758773085 Functional Loss SNV dbSNP153 33..33 33 - - - 91339 RMVar_ID_91339 Human_SNP_ID_487898983 m1A Human chr12 - 318309 318309 318309 CTCCCTGAATTACCACGACTGAAGCAAGAGCTACAACAGGCTCGGTGGTTGGACGAAGTAAGACT CTCCCTGAATTACCACGACTGAAGCAAGAGCTGCAACAGGCTCGGTGGTTGGACGAAGTAAGACT T C KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:318261..320995 32194978 MeRIP-seq:(Medium) rs762528288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1794371,Human_RBP_ID_9683134 RMVar_hsa_circ_23998,RMVar_hsa_circ_29544,RMVar_hsa_circ_277817,RMVar_hsa_circ_343114,RMVar_hsa_circ_339765,RMVar_hsa_circ_268453,RMVar_hsa_circ_154142,RMVar_hsa_circ_154143,RMVar_hsa_circ_65846,RMVar_hsa_circ_288041,RMVar_hsa_circ_39002,RMVar_hsa_circ_4169,RMVar_hsa_circ_22906,RMVar_hsa_circ_43014,RMVar_hsa_circ_154146,RMVar_hsa_circ_154147,RMVar_hsa_circ_53342,RMVar_hsa_circ_359302,RMVar_hsa_circ_367152,RMVar_hsa_circ_332307,RMVar_hsa_circ_154148,RMVar_hsa_circ_44157 91340 RMVar_ID_91340 Human_SNP_ID_487908963 m1A Human chr12 + 354142 354142 354142 TTGGGCACATCAGGTAGTGGAGGAATTAGACAAAATGTATGATAGCTGTCATCACATCCATCACA TTGGGCACATCAGGTAGTGGAGGAATTAGACACAATGTATGATAGCTGTCATCACATCCATCACA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:354092..363023 32194978 MeRIP-seq:(Medium) rs778423495 Functional Loss SNV dbSNP153 33..33 33 - - - 91341 RMVar_ID_91341 Human_SNP_ID_487908964 m1A Human chr12 + 354142 354142 354142 TTGGGCACATCAGGTAGTGGAGGAATTAGACAAAATGTATGATAGCTGTCATCACATCCATCACA TTGGGCACATCAGGTAGTGGAGGAATTAGACAGAATGTATGATAGCTGTCATCACATCCATCACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:354092..363023 32194978 MeRIP-seq:(Medium) rs778423495 Functional Loss SNV dbSNP153 33..33 33 - - - 91342 RMVar_ID_91342 Human_SNP_ID_487918089 m1A Human chr12 - 385973 385973 385973 TGTGTTTTTTTAAAAAAATCTTTCTATTTAGGACTGGCAGCCTCCATTTGCCTGTGAAGTAAAAA TGTGTTTTTTTAAAAAAATCTTTCTATTTAGGGCTGGCAGCCTCCATTTGCCTGTGAAGTAAAAA T C KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:385927..388259 32194978 MeRIP-seq:(Medium) rs1565555377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872861,Human_RBP_ID_11954519,Human_RBP_ID_19060848,Human_RBP_ID_22644531,Human_RBP_ID_24557604,Human_RBP_ID_25015179 Human_Splice_Rec_1319924,Human_Splice_Rec_1319925,Human_Splice_Rec_1320012,Human_Splice_Rec_1320013,Human_Splice_Rec_1320016,Human_Splice_Rec_1320017,Human_Splice_Rec_1320024,Human_Splice_Rec_1320025 RMVar_hsa_circ_29544,RMVar_hsa_circ_75829,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_64135,RMVar_hsa_circ_63870,RMVar_hsa_circ_343609 91343 RMVar_ID_91343 Human_SNP_ID_487919343 m1A Human chr12 - 389403 389403 389403 GGAGACAAACAGCCACACTGTGCTGCCGGGGAAGAGAAGAAGAAGGAAAGGCCAGACACACAGGC GGAGACAAACAGCCACACTGTGCTGCCGGGGAGGAGAAGAAGAAGGAAAGGCCAGACACACAGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:389352..389511 26863196 MeRIP-seq:(Medium) rs930249902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75829,RMVar_hsa_circ_154157 91344 RMVar_ID_91344 Human_SNP_ID_487919374 m1A Human chr12 - 389485 389485 389485 GAAGAGCTTGTGCCCCTCCCCGACCCCTTACCAAGGGCGAGCTGCGTGGAGTCGTTGGACTGGGC GAAGAGCTTGTGCCCCTCCCCGACCCCTTACCGAGGGCGAGCTGCGTGGAGTCGTTGGACTGGGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:389370..389518 26863196 MeRIP-seq:(Medium) rs1425237881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4225504,Human_RBP_ID_18627741,Human_RBP_ID_24974610 91345 RMVar_ID_91345 Human_SNP_ID_487922435 m1A Human chr12 + 401781 401781 401781 GTTAGGGAGAAGTAACTGCGGAAGCAGTGCGGAGGAGAGGACGTGAGCCTGAATGTGGTGTCCGT GTTAGGGAGAAGTAACTGCGGAAGCAGTGCGGGGGAGAGGACGTGAGCCTGAATGTGGTGTCCGT A G CCDC77 Ensembl:ENSG00000120647 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:401696..401862 26863196 MeRIP-seq:(Medium) rs980053367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6193787,Human_RBP_ID_18417376,Human_RBP_ID_23563353 RMVar_hsa_circ_99817,RMVar_hsa_circ_154167 91346 RMVar_ID_91346 Human_SNP_ID_487922595 m1A Human chr12 + 402411 402411 402411 AATCATTTTGGATGGGGAGACTCAGGAAAGAGAAAAAGGAGGTGGTATTTAAGATGAGTTTTCAT AATCATTTTGGATGGGGAGACTCAGGAAAGAGGAAAAGGAGGTGGTATTTAAGATGAGTTTTCAT A G CCDC77 Ensembl:ENSG00000120647 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:402403..402487 26863196 MeRIP-seq:(Medium) rs1565562290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11967033 RMVar_hsa_circ_99817,RMVar_hsa_circ_154167 91347 RMVar_ID_91347 Human_SNP_ID_487938690 m1A Human chr12 + 460127 460126 460128 GGAGAGGCGTGGGGAGGAGAGCCCGGCGCGGAACACACGCGCGGAGGAGGAGCCGGGCTCGGCTC GGAGAGGCGTGGGGAGGAGAGCCCGGCGCGGA__ACACGCGCGGAGGAGGAGCCGGGCTCGGCTC AAC A B4GALNT3 Ensembl:ENSG00000139044 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:459976..460260 26863196 MeRIP-seq:(Medium) rs1423125211 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25025045 91348 RMVar_ID_91348 Human_SNP_ID_487968675 m1A Human chr12 + 566176 566176 566176 TTGATGGGCTGGCTCCTGGGGTCGGAGCTTCCAGGCTGTAGGGGAGAAAGCACAGACTTACCAAG TTGATGGGCTGGCTCCTGGGGTCGGAGCTTCCCGGCTGTAGGGGAGAAAGCACAGACTTACCAAG A C lnc-B4GALNT3-4 RNACentral:URS00008BE936 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:566143..566214 26863196 MeRIP-seq:(Medium) rs751542444 Functional Loss SNV dbSNP153 33..33 33 - - - 91349 RMVar_ID_91349 Human_SNP_ID_487980270 m1A Human chr12 - 611194 611191 611195 AGAAAGAAAGAAAGAGGGAAAGAAAAAGAAAGAAAAGGAGGAAAGAAAAGAAGGAAAGAAAGAAA AGAAAGAAAGAAAGAGGGAAAGAAAAAGAAA____AGGAGGAAAGAAAAGAAGGAAAGAAAGAAA TTTTC T NINJ2 Ensembl:ENSG00000171840 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:611176..611271 26863196 MeRIP-seq:(Medium) rs753815215 Functional Loss DEL dbSNP153 32..35 33 - - - 91350 RMVar_ID_91350 Human_SNP_ID_487988323 m1A Human chr12 + 642944 642944 642944 CGCCCTCGCGCTCCCGGGCCCCGGCCGCCCCCACGCCCCACGCCGCGCCCGCCGGCCCGGCCCTC CGCCCTCGCGCTCCCGGGCCCCGGCCGCCCCCGCGCCCCACGCCGCGCCCGCCGGCCCGGCCCTC A G NINJ2-AS1 Ensembl:ENSG00000177406 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:642923..643204;chr12:642923..643207 26863196 MeRIP-seq:(Medium) rs1426505116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8248649 91351 RMVar_ID_91351 Human_SNP_ID_487988340 m1A Human chr12 - 642979 642979 642979 GGAAGAGGCCGCGGCGGCCGGGCCAGCTGGGGAGGGAGGGCCGGGCCGGCGGGCGCGGCGTGGGG GGAAGAGGCCGCGGCGGCCGGGCCAGCTGGGGGGGGAGGGCCGGGCCGGCGGGCGCGGCGTGGGG T C NINJ2 Ensembl:ENSG00000171840 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:642882..643009 26863410 MeRIP-seq:(Medium) rs956537288 Functional Loss SNV dbSNP153 33..33 33 - - - 91352 RMVar_ID_91352 Human_SNP_ID_487988768 m1A Human chr12 + 644506 644506 644506 ATAGACTGCAGGGCAAGGAGGGAGGGGAGAATAGTGTGGGCAGTGTACAGTGCAGAAACAAAGTT ATAGACTGCAGGGCAAGGAGGGAGGGGAGAATGGTGTGGGCAGTGTACAGTGCAGAAACAAAGTT A G NINJ2-AS1 Ensembl:ENSG00000177406 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:644458..644645 26863196 MeRIP-seq:(Medium) rs1304158141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5556735 91353 RMVar_ID_91353 Human_SNP_ID_487988784 m1A Human chr12 + 644584 644584 644584 AAAGGATTTACAGAAAGCCTGGCATACAGGGCAGGGGGACGGGGCCTGCACACGGGGCTGTTTCA AAAGGATTTACAGAAAGCCTGGCATACAGGGCGGGGGGACGGGGCCTGCACACGGGGCTGTTTCA A G NINJ2-AS1 Ensembl:ENSG00000177406 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:644518..644615 26863196 MeRIP-seq:(Medium) rs922459056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246471,Human_RBP_ID_8179640,Human_RBP_ID_8248268 91354 RMVar_ID_91354 Human_SNP_ID_488016744 m1A Human chr12 + 753246 753246 753246 CCTCCCCTCATGACTGCGGCGCCTCTGCTGCCACCGCCCGCCCGGCCGCCGCTCGCCGCAGGATG CCTCCCCTCATGACTGCGGCGCCTCTGCTGCCTCCGCCCGCCCGGCCGCCGCTCGCCGCAGGATG A T WNK1 Ensembl:ENSG00000060237 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:753163..753399 26863196 MeRIP-seq:(Medium) rs1357763357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752827,Human_RBP_ID_876873,Human_RBP_ID_4245938,Human_RBP_ID_8785822,Human_RBP_ID_9278829,Human_RBP_ID_18469293 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91355 RMVar_ID_91355 Human_SNP_ID_488016773 m1A Human chr12 - 753332 753332 753332 CGAGGCTGCTGCGGCTCACGAGGAGGGCTCGAAGGCGGGCGATTCGGGAGCTGAGCCACGGGGGT CGAGGCTGCTGCGGCTCACGAGGAGGGCTCGAGGGCGGGCGATTCGGGAGCTGAGCCACGGGGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:752601..754265 26863196 MeRIP-seq:(Medium) rs368645018 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_521 91356 RMVar_ID_91356 Human_SNP_ID_488016852 m1A Human chr12 - 753547 753545 753547 GCGCCGCCAGACATGGTCGGTTCGCTGGAGAGAGGCGAGCGGGCTCGGATTCGTGAACGAAAAGG GCGCCGCCAGACATGGTCGGTTCGCTGGAGAG__GCGAGCGGGCTCGGATTCGTGAACGAAAAGG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:753526..753550 26863196 MeRIP-seq:(Medium) rs779523515 Functional Loss DEL dbSNP153 33..34 33 - - - 91357 RMVar_ID_91357 Human_SNP_ID_488016864 m1A Human chr12 + 753558 753558 753558 ACGAATCCGAGCCCGCTCGCCTCTCTCCAGCGAACCGACCATGTCTGGCGGCGCCGCAGAGAAGC ACGAATCCGAGCCCGCTCGCCTCTCTCCAGCGTACCGACCATGTCTGGCGGCGCCGCAGAGAAGC A T WNK1 Ensembl:ENSG00000060237 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:752642..754090 32194978 MeRIP-seq:(Medium) rs1292098183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876876,Human_RBP_ID_4243085,Human_RBP_ID_6228718,Human_RBP_ID_8384888,Human_RBP_ID_8786520,Human_RBP_ID_22039115,Human_RBP_ID_27218796 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91358 RMVar_ID_91358 Human_SNP_ID_488016915 m1A Human chr12 - 753646 753646 753646 TTCTCCCCCACGGAGGAATCGGAGCTGGAGCCATTCTTGGGGGCAGGAGCCGGCGGCGAGAGGAA TTCTCCCCCACGGAGGAATCGGAGCTGGAGCCCTTCTTGGGGGCAGGAGCCGGCGGCGAGAGGAA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:753601..753675;chr12:753596..753851 26863196 MeRIP-seq:(Medium) rs72647369 Functional Loss SNV dbSNP153 33..33 33 - - - 91359 RMVar_ID_91359 Human_SNP_ID_488016955 m1A Human chr12 + 753743 753743 753743 GCAGGACCGAGGAGTACAGGCGCCGCCGCCACACTATGGACAAGGACAGCCGTGGGGCGGCCGCG GCAGGACCGAGGAGTACAGGCGCCGCCGCCACCCTATGGACAAGGACAGCCGTGGGGCGGCCGCG A C WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:753693..753813 26863196 MeRIP-seq:(Medium) rs751181069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809500,Human_RBP_ID_6228722,Human_RBP_ID_8786520,Human_RBP_ID_18189035,Human_RBP_ID_26912151,Human_RBP_ID_27218799,Human_RBP_ID_27425353 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91360 RMVar_ID_91360 Human_SNP_ID_488016956 m1A Human chr12 + 753743 753743 753743 GCAGGACCGAGGAGTACAGGCGCCGCCGCCACACTATGGACAAGGACAGCCGTGGGGCGGCCGCG GCAGGACCGAGGAGTACAGGCGCCGCCGCCACTCTATGGACAAGGACAGCCGTGGGGCGGCCGCG A T WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:753693..753813 26863196 MeRIP-seq:(Medium) rs751181069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809500,Human_RBP_ID_6228722,Human_RBP_ID_8786520,Human_RBP_ID_18189035,Human_RBP_ID_26912151,Human_RBP_ID_27218799,Human_RBP_ID_27425353 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91361 RMVar_ID_91361 Human_SNP_ID_488016993 m1A Human chr12 + 753836 753836 753836 TCCGCCGGAGCGTCATCTGTGACTCCAATGCCACTGCACTGGAGCTTCCCGGCCTTCCTCTTTCC TCCGCCGGAGCGTCATCTGTGACTCCAATGCCTCTGCACTGGAGCTTCCCGGCCTTCCTCTTTCC A T WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:753787..753980 26863196 MeRIP-seq:(Medium) rs763414550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4260312,Human_RBP_ID_8785835,Human_RBP_ID_18188651,Human_RBP_ID_18634245,Human_RBP_ID_25006897,Human_RBP_ID_26805297,Human_RBP_ID_26912153,Human_RBP_ID_27218801,Human_RBP_ID_27425357 Human_miRNA_ID_2078785,Human_miRNA_ID_2081101,Human_miRNA_ID_2091646 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91362 RMVar_ID_91362 Human_SNP_ID_488017038 m1A Human chr12 + 753924 753924 753924 GGCTGTCCCGCAGAGTGCTCCACCGGAGCCCCACCGGGAAGAGACCGTGACCGCCACCGCCACTT GGCTGTCCCGCAGAGTGCTCCACCGGAGCCCCCCCGGGAAGAGACCGTGACCGCCACCGCCACTT A C WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:753901..753925 26863196 MeRIP-seq:(Medium) rs773816207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876878,Human_RBP_ID_18188651 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91363 RMVar_ID_91363 Human_SNP_ID_488017067 m1A Human chr12 - 753976 753976 753976 ACGGCCTGTTCCCCAGGGGCGGCAGCGGCTGGAGGCTGCTGGGCTACCTGGGAAGTGGCGGTGGC ACGGCCTGTTCCCCAGGGGCGGCAGCGGCTGGGGGCTGCTGGGCTACCTGGGAAGTGGCGGTGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:753936..754152 26863196 MeRIP-seq:(Medium) rs781603632 Functional Loss SNV dbSNP153 33..33 33 - - - 91364 RMVar_ID_91364 Human_SNP_ID_488024471 m1A Human chr12 + 783015 783015 783015 AGCTTCGAACTCCTGGGCTTAAGCGATCCTCCAGCCTTAGCTTTCCAAGTAGCTGGGACTACAAG AGCTTCGAACTCCTGGGCTTAAGCGATCCTCCGGCCTTAGCTTTCCAAGTAGCTGGGACTACAAG A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:782976..783137 26863196 MeRIP-seq:(Medium) rs1302139529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25008141 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 91365 RMVar_ID_91365 Human_SNP_ID_488049975 m1A Human chr12 + 885662 885662 885662 ATGTGCCTGCTGTACAGCAGACACTAATTCATAGTCAGCCTCAACCAGCTTTGCTTCCCAACCAG ATGTGCCTGCTGTACAGCAGACACTAATTCATGGTCAGCCTCAACCAGCTTTGCTTCCCAACCAG A G WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:885626..885675 26863196 MeRIP-seq:(Medium) rs72650733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1804011,Human_RBP_ID_8386339,Human_RBP_ID_17186469,Human_RBP_ID_17241379,Human_RBP_ID_17356850,Human_RBP_ID_17474650,Human_RBP_ID_18265802,Human_RBP_ID_18434939,Human_RBP_ID_19704087,Human_RBP_ID_22913023 Human_miRNA_ID_894068,Human_miRNA_ID_900732,Human_miRNA_ID_1279423,Human_miRNA_ID_1394505,Human_miRNA_ID_2406606,Human_miRNA_ID_2406607,Human_miRNA_ID_2406608,Human_miRNA_ID_2409601,Human_miRNA_ID_2409602,Human_miRNA_ID_2409603,Human_miRNA_ID_2714846,Human_miRNA_ID_2714847,Human_miRNA_ID_2714848,Human_miRNA_ID_3050829,Human_miRNA_ID_3050830,Human_miRNA_ID_3050831 RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_98715,RMVar_hsa_circ_76827,RMVar_hsa_circ_154202,RMVar_hsa_circ_333745,RMVar_hsa_circ_371180,RMVar_hsa_circ_124909,RMVar_hsa_circ_66595,RMVar_hsa_circ_154205,RMVar_hsa_circ_154206,RMVar_hsa_circ_154207,RMVar_hsa_circ_369355,RMVar_hsa_circ_373854,RMVar_hsa_circ_99294,RMVar_hsa_circ_90841,RMVar_hsa_circ_126144,RMVar_hsa_circ_154210,RMVar_hsa_circ_154211,RMVar_hsa_circ_154212,RMVar_hsa_circ_154209,RMVar_hsa_circ_154213,RMVar_hsa_circ_368991,RMVar_hsa_circ_370009,RMVar_hsa_circ_368992,RMVar_hsa_circ_154214,RMVar_hsa_circ_343405 91366 RMVar_ID_91366 Human_SNP_ID_488049978 m1A Human chr12 + 885673 885673 885673 GTACAGCAGACACTAATTCATAGTCAGCCTCAACCAGCTTTGCTTCCCAACCAGCCCCATACTCA GTACAGCAGACACTAATTCATAGTCAGCCTCAGCCAGCTTTGCTTCCCAACCAGCCCCATACTCA A G WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:885626..885700 26863196 MeRIP-seq:(Medium) rs112113141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8386339,Human_RBP_ID_8786495,Human_RBP_ID_17186469,Human_RBP_ID_17241379,Human_RBP_ID_17356850,Human_RBP_ID_17474650,Human_RBP_ID_19704087,Human_RBP_ID_22913023 Human_miRNA_ID_894068,Human_miRNA_ID_900732,Human_miRNA_ID_907383,Human_miRNA_ID_914023,Human_miRNA_ID_1279423,Human_miRNA_ID_2406606,Human_miRNA_ID_2406607,Human_miRNA_ID_2406608,Human_miRNA_ID_2409601,Human_miRNA_ID_2409602,Human_miRNA_ID_2409603,Human_miRNA_ID_2412589,Human_miRNA_ID_2412590,Human_miRNA_ID_2412591,Human_miRNA_ID_2415562,Human_miRNA_ID_2415563,Human_miRNA_ID_2415564,Human_miRNA_ID_2624076,Human_miRNA_ID_2624077,Human_miRNA_ID_2624078 RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_98715,RMVar_hsa_circ_76827,RMVar_hsa_circ_154202,RMVar_hsa_circ_333745,RMVar_hsa_circ_371180,RMVar_hsa_circ_124909,RMVar_hsa_circ_66595,RMVar_hsa_circ_154205,RMVar_hsa_circ_154206,RMVar_hsa_circ_154207,RMVar_hsa_circ_369355,RMVar_hsa_circ_373854,RMVar_hsa_circ_99294,RMVar_hsa_circ_90841,RMVar_hsa_circ_126144,RMVar_hsa_circ_154210,RMVar_hsa_circ_154211,RMVar_hsa_circ_154212,RMVar_hsa_circ_154209,RMVar_hsa_circ_154213,RMVar_hsa_circ_368991,RMVar_hsa_circ_370009,RMVar_hsa_circ_368992,RMVar_hsa_circ_154214,RMVar_hsa_circ_343405 91367 RMVar_ID_91367 Human_SNP_ID_488049979 m1A Human chr12 + 885673 885673 885673 GTACAGCAGACACTAATTCATAGTCAGCCTCAACCAGCTTTGCTTCCCAACCAGCCCCATACTCA GTACAGCAGACACTAATTCATAGTCAGCCTCATCCAGCTTTGCTTCCCAACCAGCCCCATACTCA A T WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:885626..885700 26863196 MeRIP-seq:(Medium) rs112113141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8386339,Human_RBP_ID_8786495,Human_RBP_ID_17186469,Human_RBP_ID_17241379,Human_RBP_ID_17356850,Human_RBP_ID_17474650,Human_RBP_ID_19704087,Human_RBP_ID_22913023 Human_miRNA_ID_894068,Human_miRNA_ID_900732,Human_miRNA_ID_907383,Human_miRNA_ID_914023,Human_miRNA_ID_1279423,Human_miRNA_ID_2406606,Human_miRNA_ID_2406607,Human_miRNA_ID_2406608,Human_miRNA_ID_2409601,Human_miRNA_ID_2409602,Human_miRNA_ID_2409603,Human_miRNA_ID_2412589,Human_miRNA_ID_2412590,Human_miRNA_ID_2412591,Human_miRNA_ID_2415562,Human_miRNA_ID_2415563,Human_miRNA_ID_2415564,Human_miRNA_ID_2624076,Human_miRNA_ID_2624077,Human_miRNA_ID_2624078 RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_98715,RMVar_hsa_circ_76827,RMVar_hsa_circ_154202,RMVar_hsa_circ_333745,RMVar_hsa_circ_371180,RMVar_hsa_circ_124909,RMVar_hsa_circ_66595,RMVar_hsa_circ_154205,RMVar_hsa_circ_154206,RMVar_hsa_circ_154207,RMVar_hsa_circ_369355,RMVar_hsa_circ_373854,RMVar_hsa_circ_99294,RMVar_hsa_circ_90841,RMVar_hsa_circ_126144,RMVar_hsa_circ_154210,RMVar_hsa_circ_154211,RMVar_hsa_circ_154212,RMVar_hsa_circ_154209,RMVar_hsa_circ_154213,RMVar_hsa_circ_368991,RMVar_hsa_circ_370009,RMVar_hsa_circ_368992,RMVar_hsa_circ_154214,RMVar_hsa_circ_343405 91368 RMVar_ID_91368 Human_SNP_ID_488053941 m1A Human chr12 - 900619 900619 900619 GCTTGGTACTGAAATGGCACCATCACTGGTGAAGGCTGAATAGAGGTTGTCACTGGAGGGAGATG GCTTGGTACTGAAATGGCACCATCACTGGTGATGGCTGAATAGAGGTTGTCACTGGAGGGAGATG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:900488..900702 26863196 MeRIP-seq:(Medium) rs370128345 Functional Loss SNV dbSNP153 33..33 33 - - - 91369 RMVar_ID_91369 Human_SNP_ID_488055815 m1A Human chr12 + 908592 908590 908593 CTGCAGCATCAGCTACCTCTCTAGGTCACTTCACCAAGTCTATGTGCCCCCCACAGCAGTATGGC CTGCAGCATCAGCTACCTCTCTAGGTCACTT___CAAGTCTATGTGCCCCCCACAGCAGTATGGC TCAC T WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:908543..908763 26863196 MeRIP-seq:(Medium) rs771255174 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2297674,Human_RBP_ID_6119428,Human_RBP_ID_8065329,Human_RBP_ID_8775032,Human_RBP_ID_17235671,Human_RBP_ID_17351345,Human_RBP_ID_17467401,Human_RBP_ID_17806901,Human_RBP_ID_18254030,Human_RBP_ID_26805309 91370 RMVar_ID_91370 Human_SNP_ID_488055816 m1A Human chr12 + 908592 908592 908592 CTGCAGCATCAGCTACCTCTCTAGGTCACTTCACCAAGTCTATGTGCCCCCCACAGCAGTATGGC CTGCAGCATCAGCTACCTCTCTAGGTCACTTCGCCAAGTCTATGTGCCCCCCACAGCAGTATGGC A G WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:908543..908763 26863196 MeRIP-seq:(Medium) rs750710650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2297674,Human_RBP_ID_6119428,Human_RBP_ID_8065329,Human_RBP_ID_8775032,Human_RBP_ID_17235671,Human_RBP_ID_17351345,Human_RBP_ID_17467401,Human_RBP_ID_17806901,Human_RBP_ID_18254030,Human_RBP_ID_26805309 91371 RMVar_ID_91371 Human_SNP_ID_488055850 m1A Human chr12 + 908675 908675 908675 GGCGCTCAATGGAGTGGGACGGGTGGCCCAGCACCACAGCCACTTGGCCAGTTCCAACCTGTGGG GGCGCTCAATGGAGTGGGACGGGTGGCCCAGCCCCACAGCCACTTGGCCAGTTCCAACCTGTGGG A C WNK1 Ensembl:ENSG00000060237 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr12:908651..908675;chr12:908626..908675 26863196,32194978 MeRIP-seq:(Medium) rs756976844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_407838,Human_RBP_ID_4196365,Human_RBP_ID_6119451,Human_RBP_ID_8775034,Human_RBP_ID_17242761,Human_RBP_ID_17356861,Human_RBP_ID_19701541 Human_miRNA_ID_1356267 91372 RMVar_ID_91372 Human_SNP_ID_488056190 m1A Human chr12 + 909951 909950 909951 AAACAGAAAGTTCTGTTTCGGGAATAGTGAGGAGGGGGTGTTGTAACAAAATTGGACAACTTAAA AAACAGAAAGTTCTGTTTCGGGAATAGTGAGG_GGGGGTGTTGTAACAAAATTGGACAACTTAAA GA G WNK1 Ensembl:ENSG00000060237 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:909901..910098 26863196 MeRIP-seq:(Medium) rs1384152672 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_36364,Human_RBP_ID_407936,Human_RBP_ID_989208,Human_RBP_ID_4196484,Human_RBP_ID_6119621,Human_RBP_ID_8178391,Human_RBP_ID_17683108,Human_RBP_ID_18254078,Human_RBP_ID_23269844,Human_RBP_ID_23531765 Human_miRNA_ID_1334479 91373 RMVar_ID_91373 Human_SNP_ID_488078428 m1A Human chr12 + 990986 990986 990986 TGTGTGTGTGTGTGCAGGGACGCTCCGCGCCCATCACTCTGTTTCGGTGCTAATCGACCGCCGTG TGTGTGTGTGTGTGCAGGGACGCTCCGCGCCCTTCACTCTGTTTCGGTGCTAATCGACCGCCGTG A T ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:990939..991090 26863196 MeRIP-seq:(Medium) rs1237386938 Functional Loss SNV dbSNP153 33..33 33 - - - 91374 RMVar_ID_91374 Human_SNP_ID_488078429 m1A Human chr12 - 990987 990987 990987 CCACGGCGGTCGATTAGCACCGAAACAGAGTGATGGGCGCGGAGCGTCCCTGCACACACACACAC CCACGGCGGTCGATTAGCACCGAAACAGAGTGGTGGGCGCGGAGCGTCCCTGCACACACACACAC T C AC004803.1 Ensembl:ENSG00000250132 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:990984..991103 26863196 MeRIP-seq:(Medium) rs969982298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8248630 91375 RMVar_ID_91375 Human_SNP_ID_488078432 m1A Human chr12 - 991001 991001 991001 GGGGGAAATCGGCGCCACGGCGGTCGATTAGCACCGAAACAGAGTGATGGGCGCGGAGCGTCCCT GGGGGAAATCGGCGCCACGGCGGTCGATTAGCGCCGAAACAGAGTGATGGGCGCGGAGCGTCCCT T C AC004803.1 Ensembl:ENSG00000250132 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:990999..991090 26863410 MeRIP-seq:(Medium) rs1227247045 Functional Loss SNV dbSNP153 33..33 33 - - - 91376 RMVar_ID_91376 Human_SNP_ID_488078561 m1A Human chr12 - 991265 991247 991265 GCTGCTGCCGCCCAGGCACCGCCGCCGCCGCCACTACCGCCGCCGCCGCCGCCACAGCACGGCCC GCTGCTGCCGCCCAGGCACCGCCGCCGCCGCC__________________GCCACAGCACGGCCC CGGCGGCGGCGGCGGTAGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:991221..991432;chr12:991223..991411 26863196 MeRIP-seq:(Medium) rs1432848980 Functional Loss DEL dbSNP153 33..50 33 - - - 91377 RMVar_ID_91377 Human_SNP_ID_488078569 m1A Human chr12 - 991265 991250 991265 GCTGCTGCCGCCCAGGCACCGCCGCCGCCGCCACTACCGCCGCCGCCGCCGCCACAGCACGGCCC GCTGCTGCCGCCCAGGCACCGCCGCCGCCGCC_______________GCCGCCACAGCACGGCCC CGGCGGCGGCGGTAGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:991221..991432;chr12:991223..991411 26863196 MeRIP-seq:(Medium) rs755992278 Functional Loss DEL dbSNP153 33..47 33 - - - 91378 RMVar_ID_91378 Human_SNP_ID_488078600 m1A Human chr12 + 991298 991275 991298 GGCGGCGGCGGCGGTGCCTGGGCGGCAGCAGCAGCAGTAGCGGCAGCCCTGAGGACGGTGAGACG GGCGGCGGCG_______________________GCAGTAGCGGCAGCCCTGAGGACGGTGAGACG GGCGGTGCCTGGGCGGCAGCAGCA G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:991250..991423 26863196 MeRIP-seq:(Medium) rs1261019988 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_753010,Human_RBP_ID_4245941,Human_RBP_ID_5521304 Human_Splice_Rec_1321005,Human_Splice_Rec_1321039,Human_Splice_Rec_1321239 Human_miRNA_ID_2353683 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233 91379 RMVar_ID_91379 Human_SNP_ID_488078612 m1A Human chr12 - 991284 991284 991284 CAGGGCTGCCGCTACTGCTGCTGCTGCCGCCCAGGCACCGCCGCCGCCGCCACTACCGCCGCCGC CAGGGCTGCCGCTACTGCTGCTGCTGCCGCCCTGGCACCGCCGCCGCCGCCACTACCGCCGCCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:991234..991420 26863196 MeRIP-seq:(Medium) rs10849610 Functional Loss SNV dbSNP153 33..33 33 - - - 91380 RMVar_ID_91380 Human_SNP_ID_488078613 m1A Human chr12 - 991284 991284 991284 CAGGGCTGCCGCTACTGCTGCTGCTGCCGCCCAGGCACCGCCGCCGCCGCCACTACCGCCGCCGC CAGGGCTGCCGCTACTGCTGCTGCTGCCGCCCGGGCACCGCCGCCGCCGCCACTACCGCCGCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:991234..991420 26863196 MeRIP-seq:(Medium) rs10849610 Functional Loss SNV dbSNP153 33..33 33 - - - 91381 RMVar_ID_91381 Human_SNP_ID_488078620 m1A Human chr12 + 991292 991291 991292 GGTAGTGGCGGCGGCGGCGGTGCCTGGGCGGCAGCAGCAGCAGTAGCGGCAGCCCTGAGGACGGT GGTAGTGGCGGCGGCGGCGGTGCCTGGGCGGC_GCAGCAGCAGTAGCGGCAGCCCTGAGGACGGT CA C ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:991244..991417 26863196 MeRIP-seq:(Medium) rs1394929518 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_753010,Human_RBP_ID_4245941,Human_RBP_ID_5521304 Human_Splice_Rec_1321005,Human_Splice_Rec_1321039,Human_Splice_Rec_1321239 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233 91382 RMVar_ID_91382 Human_SNP_ID_488078622 m1A Human chr12 + 991292 991292 991292 GGTAGTGGCGGCGGCGGCGGTGCCTGGGCGGCAGCAGCAGCAGTAGCGGCAGCCCTGAGGACGGT GGTAGTGGCGGCGGCGGCGGTGCCTGGGCGGCGGCAGCAGCAGTAGCGGCAGCCCTGAGGACGGT A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:991244..991417 26863196 MeRIP-seq:(Medium) rs1374736675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753010,Human_RBP_ID_4245941,Human_RBP_ID_5521304 Human_Splice_Rec_1321005,Human_Splice_Rec_1321039,Human_Splice_Rec_1321239 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233 91383 RMVar_ID_91383 Human_SNP_ID_488078627 m1A Human chr12 + 991298 991298 991298 GGCGGCGGCGGCGGTGCCTGGGCGGCAGCAGCAGCAGTAGCGGCAGCCCTGAGGACGGTGAGACG GGCGGCGGCGGCGGTGCCTGGGCGGCAGCAGCGGCAGTAGCGGCAGCCCTGAGGACGGTGAGACG A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:991250..991423 26863196 MeRIP-seq:(Medium) rs1379030241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753010,Human_RBP_ID_4245941,Human_RBP_ID_5521304 Human_Splice_Rec_1321005,Human_Splice_Rec_1321039,Human_Splice_Rec_1321239 Human_miRNA_ID_2353683 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233 91384 RMVar_ID_91384 Human_SNP_ID_488106773 m1A Human chr12 + 1100187 1100187 1100187 TGACTTTTGAACAGACTTCAACAGTTAAGGGAAGGAGAGAGCCTGTCAAAGGGAGCAGTGAGTGA TGACTTTTGAACAGACTTCAACAGTTAAGGGAGGGAGAGAGCCTGTCAAAGGGAGCAGTGAGTGA A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:1100186..1100350 26863196 MeRIP-seq:(Medium) rs1213749480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65779,RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_317236,RMVar_hsa_circ_360114,RMVar_hsa_circ_366027,RMVar_hsa_circ_379087,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_356862,RMVar_hsa_circ_286055,RMVar_hsa_circ_310476,RMVar_hsa_circ_21731,RMVar_hsa_circ_53620,RMVar_hsa_circ_154237,RMVar_hsa_circ_352923,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_364698,RMVar_hsa_circ_355693,RMVar_hsa_circ_346249,RMVar_hsa_circ_13451,RMVar_hsa_circ_42270,RMVar_hsa_circ_154239 91385 RMVar_ID_91385 Human_SNP_ID_488143203 m1A Human chr12 + 1236836 1236836 1236836 TGAAGCACAAGGAACAGGTGGAAAAAAAGAAGAGTGCACAAATGTTAGAGGAGGCGCGACGACGG TGAAGCACAAGGAACAGGTGGAAAAAAAGAAGGGTGCACAAATGTTAGAGGAGGCGCGACGACGG A G ERC1 Ensembl:ENSG00000082805 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:1236729..1236853 26863196 MeRIP-seq:(Medium) rs746203928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5554988,Human_RBP_ID_9366028,Human_RBP_ID_17814194,Human_RBP_ID_22911942 Human_Splice_Rec_1321026,Human_Splice_Rec_1321027,Human_Splice_Rec_1321062,Human_Splice_Rec_1321063,Human_Splice_Rec_1321102,Human_Splice_Rec_1321103,Human_Splice_Rec_1321142,Human_Splice_Rec_1321143,Human_Splice_Rec_1321178,Human_Splice_Rec_1321179,Human_Splice_Rec_1321224,Human_Splice_Rec_1321225,Human_Splice_Rec_1321254,Human_Splice_Rec_1321255,Human_Splice_Rec_1321288,Human_Splice_Rec_1321289,Human_Splice_Rec_1321322,Human_Splice_Rec_1321323,Human_Splice_Rec_1321356,Human_Splice_Rec_1321357,Human_Splice_Rec_1321390,Human_Splice_Rec_1321391,Human_Splice_Rec_1321424,Human_Splice_Rec_1321425,Human_Splice_Rec_1321462,Human_Splice_Rec_1321463,Human_Splice_Rec_1321468,Human_Splice_Rec_1321469,Human_Splice_Rec_1321486,Human_Splice_Rec_1321487 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_21731,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_13451,RMVar_hsa_circ_352302,RMVar_hsa_circ_42167,RMVar_hsa_circ_62468,RMVar_hsa_circ_333398,RMVar_hsa_circ_358674,RMVar_hsa_circ_154248,RMVar_hsa_circ_267866,RMVar_hsa_circ_69245,RMVar_hsa_circ_26639,RMVar_hsa_circ_37177,RMVar_hsa_circ_154250,RMVar_hsa_circ_39259,RMVar_hsa_circ_335405,RMVar_hsa_circ_309153,RMVar_hsa_circ_376635,RMVar_hsa_circ_154252,RMVar_hsa_circ_47003,RMVar_hsa_circ_154251 91386 RMVar_ID_91386 Human_SNP_ID_488143208 m1A Human chr12 + 1236852 1236849 1236852 GGTGGAAAAAAAGAAGAGTGCACAAATGTTAGAGGAGGCGCGACGACGGGAGGACAATCTCAACG GGTGGAAAAAAAGAAGAGTGCACAAATGTT___GGAGGCGCGACGACGGGAGGACAATCTCAACG TAGA T ERC1 Ensembl:ENSG00000082805 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:1236803..1236868 26863196 MeRIP-seq:(Medium) rs756542408 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_2314750,Human_RBP_ID_4215039,Human_RBP_ID_5554988,Human_RBP_ID_9366028,Human_RBP_ID_11888338,Human_RBP_ID_22001253,Human_RBP_ID_22911942 Human_Splice_Rec_1321026,Human_Splice_Rec_1321027,Human_Splice_Rec_1321062,Human_Splice_Rec_1321063,Human_Splice_Rec_1321102,Human_Splice_Rec_1321103,Human_Splice_Rec_1321142,Human_Splice_Rec_1321143,Human_Splice_Rec_1321178,Human_Splice_Rec_1321179,Human_Splice_Rec_1321224,Human_Splice_Rec_1321225,Human_Splice_Rec_1321254,Human_Splice_Rec_1321255,Human_Splice_Rec_1321288,Human_Splice_Rec_1321289,Human_Splice_Rec_1321322,Human_Splice_Rec_1321323,Human_Splice_Rec_1321356,Human_Splice_Rec_1321357,Human_Splice_Rec_1321390,Human_Splice_Rec_1321391,Human_Splice_Rec_1321424,Human_Splice_Rec_1321425,Human_Splice_Rec_1321462,Human_Splice_Rec_1321463,Human_Splice_Rec_1321468,Human_Splice_Rec_1321469,Human_Splice_Rec_1321486,Human_Splice_Rec_1321487 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_21731,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_13451,RMVar_hsa_circ_352302,RMVar_hsa_circ_42167,RMVar_hsa_circ_62468,RMVar_hsa_circ_333398,RMVar_hsa_circ_358674,RMVar_hsa_circ_154248,RMVar_hsa_circ_267866,RMVar_hsa_circ_69245,RMVar_hsa_circ_26639,RMVar_hsa_circ_37177,RMVar_hsa_circ_154250,RMVar_hsa_circ_39259,RMVar_hsa_circ_335405,RMVar_hsa_circ_309153,RMVar_hsa_circ_376635,RMVar_hsa_circ_154252,RMVar_hsa_circ_47003,RMVar_hsa_circ_154251 91387 RMVar_ID_91387 Human_SNP_ID_488143211 m1A Human chr12 + 1236852 1236852 1236852 GGTGGAAAAAAAGAAGAGTGCACAAATGTTAGAGGAGGCGCGACGACGGGAGGACAATCTCAACG GGTGGAAAAAAAGAAGAGTGCACAAATGTTAGGGGAGGCGCGACGACGGGAGGACAATCTCAACG A G ERC1 Ensembl:ENSG00000082805 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:1236803..1236868 26863196 MeRIP-seq:(Medium) rs1285306634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2314750,Human_RBP_ID_4215039,Human_RBP_ID_5554988,Human_RBP_ID_9366028,Human_RBP_ID_11888338,Human_RBP_ID_22001253,Human_RBP_ID_22911942 Human_Splice_Rec_1321026,Human_Splice_Rec_1321027,Human_Splice_Rec_1321062,Human_Splice_Rec_1321063,Human_Splice_Rec_1321102,Human_Splice_Rec_1321103,Human_Splice_Rec_1321142,Human_Splice_Rec_1321143,Human_Splice_Rec_1321178,Human_Splice_Rec_1321179,Human_Splice_Rec_1321224,Human_Splice_Rec_1321225,Human_Splice_Rec_1321254,Human_Splice_Rec_1321255,Human_Splice_Rec_1321288,Human_Splice_Rec_1321289,Human_Splice_Rec_1321322,Human_Splice_Rec_1321323,Human_Splice_Rec_1321356,Human_Splice_Rec_1321357,Human_Splice_Rec_1321390,Human_Splice_Rec_1321391,Human_Splice_Rec_1321424,Human_Splice_Rec_1321425,Human_Splice_Rec_1321462,Human_Splice_Rec_1321463,Human_Splice_Rec_1321468,Human_Splice_Rec_1321469,Human_Splice_Rec_1321486,Human_Splice_Rec_1321487 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_21731,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_13451,RMVar_hsa_circ_352302,RMVar_hsa_circ_42167,RMVar_hsa_circ_62468,RMVar_hsa_circ_333398,RMVar_hsa_circ_358674,RMVar_hsa_circ_154248,RMVar_hsa_circ_267866,RMVar_hsa_circ_69245,RMVar_hsa_circ_26639,RMVar_hsa_circ_37177,RMVar_hsa_circ_154250,RMVar_hsa_circ_39259,RMVar_hsa_circ_335405,RMVar_hsa_circ_309153,RMVar_hsa_circ_376635,RMVar_hsa_circ_154252,RMVar_hsa_circ_47003,RMVar_hsa_circ_154251 91388 RMVar_ID_91388 Human_SNP_ID_488143221 m1A Human chr12 + 1236873 1236873 1236873 ACAAATGTTAGAGGAGGCGCGACGACGGGAGGACAATCTCAACGACAGCTCTCAGCAGCTACAGG ACAAATGTTAGAGGAGGCGCGACGACGGGAGGGCAATCTCAACGACAGCTCTCAGCAGCTACAGG A G ERC1 Ensembl:ENSG00000082805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:1236773..1236937 26863196 MeRIP-seq:(Medium) rs765763771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809715,Human_RBP_ID_991059,Human_RBP_ID_8066761,Human_RBP_ID_8779418,Human_RBP_ID_9366028,Human_RBP_ID_18257746,Human_RBP_ID_18433953 Human_Splice_Rec_1321027,Human_Splice_Rec_1321063,Human_Splice_Rec_1321103,Human_Splice_Rec_1321143,Human_Splice_Rec_1321179,Human_Splice_Rec_1321225,Human_Splice_Rec_1321255,Human_Splice_Rec_1321289,Human_Splice_Rec_1321323,Human_Splice_Rec_1321357,Human_Splice_Rec_1321391,Human_Splice_Rec_1321425,Human_Splice_Rec_1321463,Human_Splice_Rec_1321469,Human_Splice_Rec_1321487 Human_miRNA_ID_2239623,Human_miRNA_ID_2255002,Human_miRNA_ID_2704641,Human_miRNA_ID_3016915 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_21731,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_13451,RMVar_hsa_circ_352302,RMVar_hsa_circ_42167,RMVar_hsa_circ_62468,RMVar_hsa_circ_333398,RMVar_hsa_circ_358674,RMVar_hsa_circ_154248,RMVar_hsa_circ_267866,RMVar_hsa_circ_69245,RMVar_hsa_circ_26639,RMVar_hsa_circ_37177,RMVar_hsa_circ_154250,RMVar_hsa_circ_39259,RMVar_hsa_circ_335405,RMVar_hsa_circ_309153,RMVar_hsa_circ_376635,RMVar_hsa_circ_154252,RMVar_hsa_circ_47003,RMVar_hsa_circ_154251 91389 RMVar_ID_91389 Human_SNP_ID_488214207 m1A Human chr12 - 1504703 1504702 1504703 AAGGGTGGGTGCAGGTGAGGCAGGCACGGGCGAGGTCATGCAGGTGAGGCAGGTGCAGGTGAGGC AAGGGTGGGTGCAGGTGAGGCAGGCACGGGCG_GGTCATGCAGGTGAGGCAGGTGCAGGTGAGGC CT C LINC00942-001 RNACentral:URS0000537425 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:1504599..1504797 26863196 MeRIP-seq:(Medium) rs1215042100 Functional Loss DEL dbSNP153 33..33 33 - - - 91390 RMVar_ID_91390 Human_SNP_ID_488232896 m1A Human chr12 - 1574397 1574397 1574397 CTCCACCCACACCACTGCCGCCAGCCTCCCCCACCCCAGCCTCCATCCACACCGCTGCCACCAGC CTCCACCCACACCACTGCCGCCAGCCTCCCCCCCCCCAGCCTCCATCCACACCGCTGCCACCAGC T G FBXL14 Ensembl:ENSG00000171823 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:1574346..1574456 26863196 MeRIP-seq:(Medium) rs976808334 Functional Loss SNV dbSNP153 33..33 33 - - - 91391 RMVar_ID_91391 Human_SNP_ID_488233251 m1A Human chr12 + 1575455 1575455 1575455 TAAGTAGTAGATCTTTTGCATCCCTGGGGTTAATGGTTCCTTGAGCAGACACTGACACTGTGCCG TAAGTAGTAGATCTTTTGCATCCCTGGGGTTAGTGGTTCCTTGAGCAGACACTGACACTGTGCCG A G WNT5B Ensembl:ENSG00000111186 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1575453..1575556 32194978 MeRIP-seq:(Medium) rs949132748 Functional Loss SNV dbSNP153 33..33 33 - - - 91392 RMVar_ID_91392 Human_SNP_ID_488238569 m1A Human chr12 - 1594458 1594440 1594459 GCCCGCGGAGCAGCGGCGGCGGCAGGAGGCGGAGGATGCGGCAGGGGGCGTGGGCGCGGCGGCGC GCCCGCGGAGCAGCGGCGGCGGCAGGAGGCG___________________TGGGCGCGGCGGCGC ACGCCCCCTGCCGCATCCTC A FBXL14 Ensembl:ENSG00000171823 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:1594445..1594737 26863196 MeRIP-seq:(Medium) rs1173353226 Functional Loss DEL dbSNP153 32..50 33 - - - 91393 RMVar_ID_91393 Human_SNP_ID_488251185 m1A Human chr12 + 1639885 1639883 1639886 GTACGGCTACCGCTTCGCCAAGGAGTTTGTGGATGCCCGGGAGCGAGAGAAGAACTTTGCCAAAG GTACGGCTACCGCTTCGCCAAGGAGTTTGTG___GCCCGGGAGCGAGAGAAGAACTTTGCCAAAG GGAT G WNT5B Ensembl:ENSG00000111186 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1631315..1644829 32194978 MeRIP-seq:(Medium) rs760872503 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4253409 Human_Splice_Rec_1321525,Human_Splice_Rec_1321535,Human_Splice_Rec_1321543,Human_Splice_Rec_1321553 RMVar_hsa_circ_378821,RMVar_hsa_circ_7281,RMVar_hsa_circ_154270 91394 RMVar_ID_91394 Human_SNP_ID_488252683 m1A Human chr12 + 1645890 1645890 1645890 AGACCTGCTGGCTGCAGCTGGCCGAGTTCCGCAAGGTCGGGGACCGGCTGAAGGAGAAGTACGAC AGACCTGCTGGCTGCAGCTGGCCGAGTTCCGCGAGGTCGGGGACCGGCTGAAGGAGAAGTACGAC A G WNT5B Ensembl:ENSG00000111186 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1645807..1647144 32194978 MeRIP-seq:(Medium) rs1451628857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1321526,Human_Splice_Rec_1321536,Human_Splice_Rec_1321544,Human_Splice_Rec_1321554,Human_Splice_Rec_1321558,Human_Splice_Rec_1321560 RMVar_hsa_circ_378821,RMVar_hsa_circ_115068,RMVar_hsa_circ_154270,RMVar_hsa_circ_377936,RMVar_hsa_circ_379097,RMVar_hsa_circ_154272,RMVar_hsa_circ_154273,RMVar_hsa_circ_154271 91395 RMVar_ID_91395 Human_SNP_ID_488252934 m1A Human chr12 - 1646698 1646698 1646698 CTCTTACGGAACCCATCTACATTCTGGACAAGACCCTGAAGACATCGAGGTTGAAGCTGAGTTCC CTCTTACGGAACCCATCTACATTCTGGACAAGGCCCTGAAGACATCGAGGTTGAAGCTGAGTTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:1646648..1646897 32194978 MeRIP-seq:(Medium) rs1382511403 Functional Loss SNV dbSNP153 33..33 33 - - - 91396 RMVar_ID_91396 Human_SNP_ID_488253012 m1A Human chr12 - 1647044 1647044 1647044 CAGCTCAAGCTTCCCCTCCCCGGGGGTGGGGGAAGACAGTATAACGTCCACGCAGCCTGGTCATG CAGCTCAAGCTTCCCCTCCCCGGGGGTGGGGGGAGACAGTATAACGTCCACGCAGCCTGGTCATG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:1646995..1647194 32194978 MeRIP-seq:(Medium) rs1354014340 Functional Loss SNV dbSNP153 33..33 33 - - - 91397 RMVar_ID_91397 Human_SNP_ID_488264523 m1A Human chr12 + 1691093 1691081 1691093 CGCGATTCCAGAAGCGGCATCGCGGCGGCGGCAGCGGCGGCGGCTACACCGGGCTTGGCCCCCTC CGCGATTCCAGAAGCGGCATC____________GCGGCGGCGGCTACACCGGGCTTGGCCCCCTC CGCGGCGGCGGCA C ADIPOR2 Ensembl:ENSG00000006831 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:1691083..1691197 26863196 MeRIP-seq:(Medium) rs958757118 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_4216104 Human_Splice_Rec_1321569 91398 RMVar_ID_91398 Human_SNP_ID_488264538 m1A Human chr12 - 1691105 1691105 1691105 GAACGGAGGAGGGAGGGGGCCAAGCCCGGTGTAGCCGCCGCCGCTGCCGCCGCCGCGATGCCGCT GAACGGAGGAGGGAGGGGGCCAAGCCCGGTGTGGCCGCCGCCGCTGCCGCCGCCGCGATGCCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:1691034..1691241 26863196 MeRIP-seq:(Medium) rs1261455700 Functional Loss SNV dbSNP153 33..33 33 - - - 91399 RMVar_ID_91399 Human_SNP_ID_488264539 m1A Human chr12 + 1691106 1691106 1691106 GCGGCATCGCGGCGGCGGCAGCGGCGGCGGCTACACCGGGCTTGGCCCCCTCCCTCCTCCGTTCC GCGGCATCGCGGCGGCGGCAGCGGCGGCGGCTGCACCGGGCTTGGCCCCCTCCCTCCTCCGTTCC A G ADIPOR2 Ensembl:ENSG00000006831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:1691056..1691384;chr12:1691056..1691281 26863196 MeRIP-seq:(Medium) rs1027869175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4216104,Human_RBP_ID_5461669 Human_Splice_Rec_1321569 91400 RMVar_ID_91400 Human_SNP_ID_488264540 m1A Human chr12 + 1691106 1691106 1691106 GCGGCATCGCGGCGGCGGCAGCGGCGGCGGCTACACCGGGCTTGGCCCCCTCCCTCCTCCGTTCC GCGGCATCGCGGCGGCGGCAGCGGCGGCGGCTTCACCGGGCTTGGCCCCCTCCCTCCTCCGTTCC A T ADIPOR2 Ensembl:ENSG00000006831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:1691056..1691384;chr12:1691056..1691281 26863196 MeRIP-seq:(Medium) rs1027869175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4216104,Human_RBP_ID_5461669 Human_Splice_Rec_1321569 91401 RMVar_ID_91401 Human_SNP_ID_488264556 m1A Human chr12 - 1691153 1691148 1691153 TCTCGGACTTCTTGGGAGCCACCGCTGAGGGGAGGGGGGAGGAGGGGGGAACGGAGGAGGGAGGG TCTCGGACTTCTTGGGAGCCACCGCTGAGGGG_____GGAGGAGGGGGGAACGGAGGAGGGAGGG CCCCCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1691081..1702953 32194978 MeRIP-seq:(Medium) rs1421411773 Functional Loss DEL dbSNP153 33..37 33 - - - 91402 RMVar_ID_91402 Human_SNP_ID_488285219 m1A Human chr12 - 1771408 1771408 1771408 ACCTTTCATTACTGCTACCCACAAGCCCCGGGACCTTTTTTTTTTTTTAGTTTGAGACAGCGTTT ACCTTTCATTACTGCTACCCACAAGCCCCGGGGCCTTTTTTTTTTTTTAGTTTGAGACAGCGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:1771404..1771487 26863196 MeRIP-seq:(Medium) rs1348404034 Functional Loss SNV dbSNP153 33..33 33 - - - 91403 RMVar_ID_91403 Human_SNP_ID_488285220 m1A Human chr12 - 1771408 1771408 1771408 ACCTTTCATTACTGCTACCCACAAGCCCCGGGACCTTTTTTTTTTTTTAGTTTGAGACAGCGTTT ACCTTTCATTACTGCTACCCACAAGCCCCGGGCCCTTTTTTTTTTTTTAGTTTGAGACAGCGTTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:1771404..1771487 26863196 MeRIP-seq:(Medium) rs1348404034 Functional Loss SNV dbSNP153 33..33 33 - - - 91404 RMVar_ID_91404 Human_SNP_ID_488288816 m1A Human chr12 - 1786828 1786828 1786828 CTGAGAAAACACATACCACTCCCCTCTACCTCAGGCCTCCCAAAGGGAGTGGTCATGTCACCACT CTGAGAAAACACATACCACTCCCCTCTACCTCGGGCCTCCCAAAGGGAGTGGTCATGTCACCACT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:1786651..1786875 32194978 MeRIP-seq:(Medium) rs549458954 Functional Loss SNV dbSNP153 33..33 33 - - - 91405 RMVar_ID_91405 Human_SNP_ID_488289001 m1A Human chr12 - 1787711 1787711 1787711 TCCCATATTCCCAAACACCTACTGAGGACGCCAGTCCCCATGCTCAGGACCTCCATATTTAGTTC TCCCATATTCCCAAACACCTACTGAGGACGCCGGTCCCCATGCTCAGGACCTCCATATTTAGTTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1787581..1787981 32194978 MeRIP-seq:(Medium) rs758828785 Functional Loss SNV dbSNP153 33..33 33 - - - 91406 RMVar_ID_91406 Human_SNP_ID_488289153 m1A Human chr12 - 1788329 1788327 1788329 GTTCTCAGCGAGCACTGTCAGGTCAAGTGCACATGAGGCTGTTGGTAGTGAGCTGCACGTAGACA GTTCTCAGCGAGCACTGTCAGGTCAAGTGCAC__GAGGCTGTTGGTAGTGAGCTGCACGTAGACA CAT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1788279..1788379 32194978 MeRIP-seq:(Medium) rs1353631821 Functional Loss DEL dbSNP153 33..34 33 - - - 91407 RMVar_ID_91407 Human_SNP_ID_488289155 m1A Human chr12 - 1788329 1788329 1788329 GTTCTCAGCGAGCACTGTCAGGTCAAGTGCACATGAGGCTGTTGGTAGTGAGCTGCACGTAGACA GTTCTCAGCGAGCACTGTCAGGTCAAGTGCACCTGAGGCTGTTGGTAGTGAGCTGCACGTAGACA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:1788279..1788379 32194978 MeRIP-seq:(Medium) rs977290186 Functional Loss SNV dbSNP153 33..33 33 - - - 91408 RMVar_ID_91408 Human_SNP_ID_488289173 m1A Human chr12 + 1788405 1788405 1788405 TGGCGCCTGAATGCCTTACTCTCAGCAGTCAGAGGCTTGCTTGCTCTGTGCAGATTTTTAATTTT TGGCGCCTGAATGCCTTACTCTCAGCAGTCAGGGGCTTGCTTGCTCTGTGCAGATTTTTAATTTT A G ADIPOR2 Ensembl:ENSG00000006831 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:1788079..1788529 32194978 MeRIP-seq:(Medium) rs1384761354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_416144,Human_RBP_ID_6161168,Human_RBP_ID_17237520,Human_RBP_ID_17353401,Human_RBP_ID_17470011,Human_RBP_ID_17815120,Human_RBP_ID_18258078 RMVar_hsa_circ_86037,RMVar_hsa_circ_154282,RMVar_hsa_circ_154284,RMVar_hsa_circ_121493 91409 RMVar_ID_91409 Human_SNP_ID_488344855 m1A Human chr12 - 2004399 2004399 2004399 ATGGCAGCCGTGGCGGCAGGCGGCCTGGTGGGAAAGGGGCGCGACATCAGCCTAGCGGCCCTGCA ATGGCAGCCGTGGCGGCAGGCGGCCTGGTGGGGAAGGGGCGCGACATCAGCCTAGCGGCCCTGCA T C DCP1B Ensembl:ENSG00000151065 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:2004229..2004436 26863196 MeRIP-seq:(Medium) rs1198433262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753927,Human_RBP_ID_811827,Human_RBP_ID_5140033,Human_RBP_ID_9364505,Human_RBP_ID_9415800,Human_RBP_ID_18417217,Human_RBP_ID_18434003,Human_RBP_ID_18976633 RMVar_hsa_circ_127554,RMVar_hsa_circ_154287 91410 RMVar_ID_91410 Human_SNP_ID_488543937 m1A Human chr12 + 2795067 2795067 2795067 GCCGCGCCCGGCCTCCCGCACGCCCCGCAGGTAGCGCCCCCGCCCGCGGCCCAGAGTGCGCTCGC GCCGCGCCCGGCCTCCCGCACGCCCCGCAGGTGGCGCCCCCGCCCGCGGCCCAGAGTGCGCTCGC A G FKBP4 Ensembl:ENSG00000004478 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:2794976..2795175;chr12:2794976..2795250 26863410 MeRIP-seq:(Medium) rs1324733194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4218415,Human_RBP_ID_8780347,Human_RBP_ID_9278838,Human_RBP_ID_9322400,Human_RBP_ID_22437530,Human_RBP_ID_26905353 91411 RMVar_ID_91411 Human_SNP_ID_488544184 m1A Human chr12 - 2795722 2795722 2795722 GGGGAGTCGCTCCCCGTCCTGGCCCGTGTTCCACCGCCCGGGTGGGCGAGCCCTGGCACCGCCAC GGGGAGTCGCTCCCCGTCCTGGCCCGTGTTCCGCCGCCCGGGTGGGCGAGCCCTGGCACCGCCAC T C ITFG2-AS1 Ensembl:ENSG00000256150 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:2795715..2796075 26863196 MeRIP-seq:(Medium) rs1192115912 Functional Loss SNV dbSNP153 33..33 33 - - - 91412 RMVar_ID_91412 Human_SNP_ID_488545222 m1A Human chr12 - 2799226 2799226 2799226 TGCCCACCCCTCACCTGGGCTTGAGGTACACGATGGAATGTTCTCCTTTCTCCATGCGCTGAATG TGCCCACCCCTCACCTGGGCTTGAGGTACACGGTGGAATGTTCTCCTTTCTCCATGCGCTGAATG T C ITFG2-AS1,ITFG2-AS1:2,AC005841.1 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325,Ensembl:ENSG00000258092 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:2799176..2799250 26863196 MeRIP-seq:(Medium) rs1246852961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5173340 91413 RMVar_ID_91413 Human_SNP_ID_488545401 m1A Human chr12 + 2799939 2799939 2799939 GAAATATGAATTACACCTCAAGAGTTTTGAAAAGGTAAGTTTGCTCAGGGTCTTCCCATCTAAAG GAAATATGAATTACACCTCAAGAGTTTTGAAAGGGTAAGTTTGCTCAGGGTCTTCCCATCTAAAG A G FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:2799895..2799987;chr12:2799932..2800029 26863196 MeRIP-seq:(Medium) rs1482040025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1324740,Human_Splice_Rec_1324741,Human_Splice_Rec_1324758,Human_Splice_Rec_1324759 RMVar_hsa_circ_60567,RMVar_hsa_circ_360416,RMVar_hsa_circ_302162,RMVar_hsa_circ_358417,RMVar_hsa_circ_154317 91414 RMVar_ID_91414 Human_SNP_ID_488545778 m1A Human chr12 + 2801226 2801226 2801226 ACTGGCACGGGCTGATTTCCAGAAGGTCCTGCAGCTCTACCCCAACAACAAAGCCGCCAAGACCC ACTGGCACGGGCTGATTTCCAGAAGGTCCTGCTGCTCTACCCCAACAACAAAGCCGCCAAGACCC A T FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:2801176..2801375 32194978 MeRIP-seq:(Medium) rs765115246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1470220,Human_RBP_ID_1793393,Human_RBP_ID_6172318,Human_RBP_ID_8373578,Human_RBP_ID_22435731,Human_RBP_ID_26805326,Human_RBP_ID_26905389,Human_RBP_ID_27213601,Human_RBP_ID_27421192 Human_miRNA_ID_1022924 91415 RMVar_ID_91415 Human_SNP_ID_488545815 m1A Human chr12 + 2801322 2801322 2801322 GCAGCTTGCCCGGGAGAAGAAGCTCTATGCCAATATGTTTGAGAGGCTGGCTGAGGAGGAGAACA GCAGCTTGCCCGGGAGAAGAAGCTCTATGCCACTATGTTTGAGAGGCTGGCTGAGGAGGAGAACA A C FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2801155..2801387 26863196 MeRIP-seq:(Medium) rs754477446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229622,Human_RBP_ID_1470221,Human_RBP_ID_1793394,Human_RBP_ID_3402620,Human_RBP_ID_8373579,Human_RBP_ID_8787111,Human_RBP_ID_11917326,Human_RBP_ID_17816776,Human_RBP_ID_18160137 Human_Splice_Rec_1324747,Human_Splice_Rec_1324763 Human_miRNA_ID_1099874 91416 RMVar_ID_91416 Human_SNP_ID_488545816 m1A Human chr12 + 2801322 2801322 2801322 GCAGCTTGCCCGGGAGAAGAAGCTCTATGCCAATATGTTTGAGAGGCTGGCTGAGGAGGAGAACA GCAGCTTGCCCGGGAGAAGAAGCTCTATGCCAGTATGTTTGAGAGGCTGGCTGAGGAGGAGAACA A G FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2801155..2801387 26863196 MeRIP-seq:(Medium) rs754477446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229622,Human_RBP_ID_1470221,Human_RBP_ID_1793394,Human_RBP_ID_3402620,Human_RBP_ID_8373579,Human_RBP_ID_8787111,Human_RBP_ID_11917326,Human_RBP_ID_17816776,Human_RBP_ID_18160137 Human_Splice_Rec_1324747,Human_Splice_Rec_1324763 Human_miRNA_ID_1099874 91417 RMVar_ID_91417 Human_SNP_ID_488545820 m1A Human chr12 + 2801343 2801341 2801344 GCTCTATGCCAATATGTTTGAGAGGCTGGCTGAGGAGGAGAACAAGGTGAGGATTGGGGTGGGGA GCTCTATGCCAATATGTTTGAGAGGCTGGCT___GAGGAGAACAAGGTGAGGATTGGGGTGGGGA TGAG T FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:2801292..2801384 26863196 MeRIP-seq:(Medium) rs752845341 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_809968,Human_RBP_ID_8373580,Human_RBP_ID_11917327,Human_RBP_ID_17816776,Human_RBP_ID_18160137 Human_Splice_Rec_1324747,Human_Splice_Rec_1324763 91418 RMVar_ID_91418 Human_SNP_ID_488546420 m1A Human chr12 + 2803200 2803197 2803200 CTCAGGAGACCATCCCACTGACACAGAGATGAAGGAGGAGCAGAAGAGCAACACGGCAGGGAGCC CTCAGGAGACCATCCCACTGACACAGAGAT___GGAGGAGCAGAAGAGCAACACGGCAGGGAGCC TGAA T FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2803120..2803291 26863196 MeRIP-seq:(Medium) rs746579974 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_6172320,Human_RBP_ID_9364515,Human_RBP_ID_11917344,Human_RBP_ID_23555182 Human_Splice_Rec_1324748,Human_Splice_Rec_1324765 91419 RMVar_ID_91419 Human_SNP_ID_488546606 m1A Human chr12 - 2803785 2803785 2803785 GGAAATACCAGAACAGGGAACAGGGGGTGGTCACCATGACACCAGAAGACATCATCAGCCACACC GGAAATACCAGAACAGGGAACAGGGGGTGGTCCCCATGACACCAGAAGACATCATCAGCCACACC T G ITFG2-AS1,ITFG2-AS1:2,AC005841.1 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325,Ensembl:ENSG00000258092 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2803576..2803900 26863196 MeRIP-seq:(Medium) rs951912476 Functional Loss SNV dbSNP153 33..33 33 - - - 91420 RMVar_ID_91420 Human_SNP_ID_488546611 m1A Human chr12 - 2803796 2803794 2803796 AAACTGACAGGGGAAATACCAGAACAGGGAACAGGGGGTGGTCACCATGACACCAGAAGACATCA AAACTGACAGGGGAAATACCAGAACAGGGAAC__GGGGTGGTCACCATGACACCAGAAGACATCA CCT C ITFG2-AS1,ITFG2-AS1:2,AC005841.1 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325,Ensembl:ENSG00000258092 lincRNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:2803776..2803800 26863196 MeRIP-seq:(Medium) rs534905546 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1324773 91421 RMVar_ID_91421 Human_SNP_ID_488546614 m1A Human chr12 - 2803796 2803796 2803796 AAACTGACAGGGGAAATACCAGAACAGGGAACAGGGGGTGGTCACCATGACACCAGAAGACATCA AAACTGACAGGGGAAATACCAGAACAGGGAACGGGGGGTGGTCACCATGACACCAGAAGACATCA T C ITFG2-AS1,ITFG2-AS1:2,AC005841.1 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325,Ensembl:ENSG00000258092 lincRNA,lincRNA,lincRNA intron,intron,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:2803776..2803800 26863196 MeRIP-seq:(Medium) rs1417644722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1324773 91422 RMVar_ID_91422 Human_SNP_ID_488546616 m1A Human chr12 - 2803799 2803799 2803799 GGGAAACTGACAGGGGAAATACCAGAACAGGGAACAGGGGGTGGTCACCATGACACCAGAAGACA GGGAAACTGACAGGGGAAATACCAGAACAGGGGACAGGGGGTGGTCACCATGACACCAGAAGACA T C ITFG2-AS1,ITFG2-AS1:2,AC005841.1 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325,Ensembl:ENSG00000258092 lincRNA,lincRNA,lincRNA intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:2803751..2803825 32194978 MeRIP-seq:(Medium) rs1479061128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1324773 91423 RMVar_ID_91423 Human_SNP_ID_488552830 m1A Human chr12 + 2825510 2825510 2825510 GACCTTGTGGAGCAAGGCAGTGAGGGCGAGGAAAGCTTTTAGGATTTTGAGACCAGGTGCTATGG GACCTTGTGGAGCAAGGCAGTGAGGGCGAGGACAGCTTTTAGGATTTTGAGACCAGGTGCTATGG A C ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:2825486..2825600 26863196 MeRIP-seq:(Medium) rs926535541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6172467,Human_RBP_ID_11917611,Human_RBP_ID_23555246 RMVar_hsa_circ_1008,RMVar_hsa_circ_124994,RMVar_hsa_circ_154320,RMVar_hsa_circ_69809,RMVar_hsa_circ_292503,RMVar_hsa_circ_282583,RMVar_hsa_circ_154333,RMVar_hsa_circ_154334 91424 RMVar_ID_91424 Human_SNP_ID_488562490 m1A Human chr12 + 2858851 2858848 2858851 GAGCCTGGCTTGGGGACGTCTATATCTGAGGGAGAAGAGTTGCCAAAGGGGACGGAGATGAGGTC GAGCCTGGCTTGGGGACGTCTATATCTGAG___GAAGAGTTGCCAAAGGGGACGGAGATGAGGTC GGGA G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:2858826..2858850 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 31..33 33 - - - 91425 RMVar_ID_91425 Human_SNP_ID_488562492 m1A Human chr12 + 2858851 2858851 2858851 GAGCCTGGCTTGGGGACGTCTATATCTGAGGGAGAAGAGTTGCCAAAGGGGACGGAGATGAGGTC GAGCCTGGCTTGGGGACGTCTATATCTGAGGGCGAAGAGTTGCCAAAGGGGACGGAGATGAGGTC A C ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:2858826..2858850 26863196 MeRIP-seq:(Medium) rs1187700995 Functional Loss SNV dbSNP153 33..33 33 - - - 91426 RMVar_ID_91426 Human_SNP_ID_488562525 m1A Human chr12 + 2858921 2858921 2858921 GTTCTGAACTGAGGAGCCTTTGCGGTGATTCAAGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG GTTCTGAACTGAGGAGCCTTTGCGGTGATTCAGGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:2858901..2858925;chr12:2858876..2858975;chr12:2858872..2859052 26863196 MeRIP-seq:(Medium) rs563190488 Functional Loss SNV dbSNP153 33..33 33 - - - 91427 RMVar_ID_91427 Human_SNP_ID_488562526 m1A Human chr12 + 2858921 2858921 2858921 GTTCTGAACTGAGGAGCCTTTGCGGTGATTCAAGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG GTTCTGAACTGAGGAGCCTTTGCGGTGATTCATGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG A T ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:2858901..2858925;chr12:2858876..2858975;chr12:2858872..2859052 26863196 MeRIP-seq:(Medium) rs563190488 Functional Loss SNV dbSNP153 33..33 33 - - - 91428 RMVar_ID_91428 Human_SNP_ID_488564188 m1A Human chr12 - 2864400 2864400 2864400 TGAACCAGTCACTGGTGTTGCAGCCCTCGGTGAAGGTGCCATTGCCCCTGGCGGCTTCCCTCATG TGAACCAGTCACTGGTGTTGCAGCCCTCGGTGGAGGTGCCATTGCCCCTGGCGGCTTCCCTCATG T C FOXM1 Ensembl:ENSG00000111206 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2864351..2864522 26863196 MeRIP-seq:(Medium) rs1317362780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_417988,Human_RBP_ID_5256571,Human_RBP_ID_8780434,Human_RBP_ID_9364521,Human_RBP_ID_18624898,Human_RBP_ID_18975249 Human_Splice_Rec_1325020,Human_Splice_Rec_1325021,Human_Splice_Rec_1325023,Human_Splice_Rec_1325036,Human_Splice_Rec_1325037,Human_Splice_Rec_1325052,Human_Splice_Rec_1325053,Human_Splice_Rec_1325068,Human_Splice_Rec_1325069,Human_Splice_Rec_1325078,Human_Splice_Rec_1325079,Human_Splice_Rec_1325082,Human_Splice_Rec_1325090 Human_miRNA_ID_2134201,Human_miRNA_ID_2134202 RMVar_hsa_circ_91591,RMVar_hsa_circ_106726,RMVar_hsa_circ_121592,RMVar_hsa_circ_41262,RMVar_hsa_circ_154335,RMVar_hsa_circ_154337,RMVar_hsa_circ_154336,RMVar_hsa_circ_314039,RMVar_hsa_circ_369612,RMVar_hsa_circ_47724,RMVar_hsa_circ_154339,RMVar_hsa_circ_154340,RMVar_hsa_circ_154341 91429 RMVar_ID_91429 Human_SNP_ID_488564735 m1A Human chr12 - 2866360 2866360 2866360 GTGAATGCCCTGCTTTCCTCTAAATAGGGCCTAAGTTGGAGGTTGTCATAGCCATCTCAAAAGGA GTGAATGCCCTGCTTTCCTCTAAATAGGGCCTCAGTTGGAGGTTGTCATAGCCATCTCAAAAGGA T G FOXM1 Ensembl:ENSG00000111206 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2866358..2866440 26863196 MeRIP-seq:(Medium) rs199517222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11919647,Human_RBP_ID_19057413 RMVar_hsa_circ_82979,RMVar_hsa_circ_91591,RMVar_hsa_circ_121592,RMVar_hsa_circ_41262,RMVar_hsa_circ_154335,RMVar_hsa_circ_154336,RMVar_hsa_circ_314039,RMVar_hsa_circ_369612,RMVar_hsa_circ_154339,RMVar_hsa_circ_154340,RMVar_hsa_circ_154341,RMVar_hsa_circ_98493,RMVar_hsa_circ_154342,RMVar_hsa_circ_154343 91430 RMVar_ID_91430 Human_SNP_ID_488567550 m1A Human chr12 - 2876970 2876970 2876970 CCTGGCTCGGCCCCCAGGTTGGAGGAGCCCGGAGCCCGCCTTCGGAGCTACGGCCTAACGGCGGC CCTGGCTCGGCCCCCAGGTTGGAGGAGCCCGGGGCCCGCCTTCGGAGCTACGGCCTAACGGCGGC T C FOXM1 Ensembl:ENSG00000111206 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:2876901..2877150 26863196 MeRIP-seq:(Medium) rs1195033197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418010,Human_RBP_ID_4218884 Human_Splice_Rec_1325007,Human_Splice_Rec_1325025,Human_Splice_Rec_1325039,Human_Splice_Rec_1325057 91431 RMVar_ID_91431 Human_SNP_ID_488567705 m1A Human chr12 - 2877281 2877281 2877281 CCCCCACAAGCCGGCCTGCGGTCCGCCTTACCAGCCCGGGCCGGACGGGGCCGCAGCTCCTGGCA CCCCCACAAGCCGGCCTGCGGTCCGCCTTACCGGCCCGGGCCGGACGGGGCCGCAGCTCCTGGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2877239..2877990 32194978 MeRIP-seq:(Medium) rs546106195 Functional Loss SNV dbSNP153 33..33 33 - - - 91432 RMVar_ID_91432 Human_SNP_ID_488571032 m1A Human chr12 + 2888327 2888327 2888327 CACACTGGCACTCCTAATAGCCCAGAGCCTGGACCTGTTCTGGTTAAAGACACCCCCGAGGACAA CACACTGGCACTCCTAATAGCCCAGAGCCTGGGCCTGTTCTGGTTAAAGACACCCCCGAGGACAA A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2888027..2888376 32194978 MeRIP-seq:(Medium) rs760560765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228497,Human_RBP_ID_1470377,Human_RBP_ID_1793560,Human_RBP_ID_6173591,Human_RBP_ID_11919989,Human_RBP_ID_26805333 Human_miRNA_ID_2892119 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 91433 RMVar_ID_91433 Human_SNP_ID_488571277 m1A Human chr12 + 2889222 2889218 2889222 CTTGACTCATCTGCTGAAAAGGCAAGAAGAAGAAAGGGCAGCAAGCCCTGTTTTAGGGACTACAT CTTGACTCATCTGCTGAAAAGGCAAGAAG____AAGGGCAGCAAGCCCTGTTTTAGGGACTACAT GAAGA G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2889173..2889373 32194978 MeRIP-seq:(Medium) rs368622028 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 91434 RMVar_ID_91434 Human_SNP_ID_488571842 m1A Human chr12 - 2890925 2890923 2890925 AAGCCTCCATGCCCGCCACCGAGGAAGCCCCCACCACGTACACACTCTTCCCCGCCGTCGCTAGA AAGCCTCCATGCCCGCCACCGAGGAAGCCCCC__CACGTACACACTCTTCCCCGCCGTCGCTAGA GGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:2890905..2891034 26863196 MeRIP-seq:(Medium) rs759468438 Functional Loss DEL dbSNP153 33..34 33 - - - 91435 RMVar_ID_91435 Human_SNP_ID_488571872 m1A Human chr12 - 2890949 2890949 2890949 CGCTGGGACTGAGCCGGCAGCGCGAAGCCTCCATGCCCGCCACCGAGGAAGCCCCCACCACGTAC CGCTGGGACTGAGCCGGCAGCGCGAAGCCTCCCTGCCCGCCACCGAGGAAGCCCCCACCACGTAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2877272..2909600 26863196 MeRIP-seq:(Medium) rs747888348 Functional Loss SNV dbSNP153 33..33 33 - - - 91436 RMVar_ID_91436 Human_SNP_ID_488571873 m1A Human chr12 + 2890952 2890952 2890952 CGTGGTGGGGGCTTCCTCGGTGGCGGGCATGGAGGCTTCGCGCTGCCGGCTCAGTCCCAGCGGCG CGTGGTGGGGGCTTCCTCGGTGGCGGGCATGGCGGCTTCGCGCTGCCGGCTCAGTCCCAGCGGCG A C TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:2877259..2920847;chr12:2877252..2920847;chr12:2877272..2909575 26863196 MeRIP-seq:(Medium) rs755991024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27421312 Human_Splice_Rec_1325167,Human_Splice_Rec_1325183,Human_Splice_Rec_1325197,Human_Splice_Rec_1325217 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 91437 RMVar_ID_91437 Human_SNP_ID_488583766 m1A Human chr12 + 2933459 2933459 2933459 CTTGCAGCTAGAAAGCGGAAAAAGAGCAAAACAGCCAACTACCTTATCTCCATTGATCCAGTTGA CTTGCAGCTAGAAAGCGGAAAAAGAGCAAAACTGCCAACTACCTTATCTCCATTGATCCAGTTGA A T TULP3 Ensembl:ENSG00000078246 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2931184..2933461 32194978 MeRIP-seq:(Medium) rs1565508245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25015209 Human_Splice_Rec_1325154,Human_Splice_Rec_1325155,Human_Splice_Rec_1325158,Human_Splice_Rec_1325159,Human_Splice_Rec_1325190,Human_Splice_Rec_1325191,Human_Splice_Rec_1325208,Human_Splice_Rec_1325209,Human_Splice_Rec_1325228,Human_Splice_Rec_1325229 Human_miRNA_ID_133894,Human_miRNA_ID_1984882,Human_miRNA_ID_2168440,Human_miRNA_ID_2169963 RMVar_hsa_circ_154351,RMVar_hsa_circ_351101,RMVar_hsa_circ_118065,RMVar_hsa_circ_9094,RMVar_hsa_circ_368291,RMVar_hsa_circ_3949,RMVar_hsa_circ_269124,RMVar_hsa_circ_328393,RMVar_hsa_circ_282374,RMVar_hsa_circ_359286,RMVar_hsa_circ_154356 91438 RMVar_ID_91438 Human_SNP_ID_488585817 m1A Human chr12 + 2940677 2940677 2940677 GCTGCTCCCTCAGACCTCCCTTCTGTGGACTGACCTCTCACCTCCGCCTGTTGTTCCTGCACCAC GCTGCTCCCTCAGACCTCCCTTCTGTGGACTGGCCTCTCACCTCCGCCTGTTGTTCCTGCACCAC A G TULP3 Ensembl:ENSG00000078246 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2940576..2940700 32194978 MeRIP-seq:(Medium) rs1369348199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418059,Human_RBP_ID_27421321,Human_RBP_ID_27557908 Human_miRNA_ID_641680 91439 RMVar_ID_91439 Human_SNP_ID_488591281 m1A Human chr12 - 2959458 2959458 2959458 GCCTCTCACCTGGCGGGACGCGGCGGCGCCGGAGCTGCGGCCCTCCCGCCCCCTGGCCTCGAGTG GCCTCTCACCTGGCGGGACGCGGCGGCGCCGGTGCTGCGGCCCTCCCGCCCCCTGGCCTCGAGTG T A lnc-FOXM1-2,lnc-FOXM1-2:2,lnc-FOXM1-2:3,lnc-FOXM1-2:4,lnc-FOXM1-2:5 RNACentral:URS0000D5B8C4,RNACentral:URS0000D58A3A,RNACentral:URS00009B434D,RNACentral:URS00008B328B,RNACentral:URS0000D5D24B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:2959401..2959500;chr12:2959342..2959841;chr12:2959336..2959815;chr12:2959421..2959801 26863196 MeRIP-seq:(Medium) rs1330188205 Functional Loss SNV dbSNP153 33..33 33 - - - 91440 RMVar_ID_91440 Human_SNP_ID_488592701 m1A Human chr12 - 2963901 2963901 2963901 AGTTTGGGTCAAAGGAAGCAGAGTCCCCACCCATGGGGGCCCGCCTGCCCACACCAAGCCAAGGA AGTTTGGGTCAAAGGAAGCAGAGTCCCCACCCGTGGGGGCCCGCCTGCCCACACCAAGCCAAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:2963900..2964032 26863196 MeRIP-seq:(Medium) rs1454412647 Functional Loss SNV dbSNP153 33..33 33 - - - 91441 RMVar_ID_91441 Human_SNP_ID_488598223 m1A Human chr12 - 2984156 2984156 2984156 CATACCTTCCGCACACAGGCACCACCCTCTGTACTTCCTTCTTTGAACCCACCTCCAAGCCCCAA CATACCTTCCGCACACAGGCACCACCCTCTGTGCTTCCTTCTTTGAACCCACCTCCAAGCCCCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:2984154..2984253 26863196 MeRIP-seq:(Medium) rs1336899327 Functional Loss SNV dbSNP153 33..33 33 - - - 91442 RMVar_ID_91442 Human_SNP_ID_488601266 m1A Human chr12 + 2994703 2994703 2994703 TGCCTTCATCCCGTGGCCCACGCAGTTCTTCCACTGCTCACCGGGGCTGTGGTTCCTGTCCCCAC TGCCTTCATCCCGTGGCCCACGCAGTTCTTCCGCTGCTCACCGGGGCTGTGGTTCCTGTCCCCAC A G TEAD4 Ensembl:ENSG00000197905 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2994699..2994923 26863196 MeRIP-seq:(Medium) rs973577521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22538444 91443 RMVar_ID_91443 Human_SNP_ID_488601321 m1A Human chr12 - 2994841 2994840 2994842 TCGATGGGCTTGTCCAGTGCCTGACTGCCCCCAGAGGCGGTGCTCCCCTCAGGGGAGGTGGGAGA TCGATGGGCTTGTCCAGTGCCTGACTGCCCC__GAGGCGGTGCTCCCCTCAGGGGAGGTGGGAGA CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:2994726..2994880 26863196 MeRIP-seq:(Medium) rs1380070814 Functional Loss DEL dbSNP153 32..33 33 - - - 91444 RMVar_ID_91444 Human_SNP_ID_488602068 m1A Human chr12 - 2997548 2997548 2997548 GCTCCCCAGCCAAGCCACCTGCCCTTCCCTACACTCCCCCTGCCCTTTCTCATTTCACACCTAAG GCTCCCCAGCCAAGCCACCTGCCCTTCCCTACGCTCCCCCTGCCCTTTCTCATTTCACACCTAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:2997545..2997712 26863196 MeRIP-seq:(Medium) rs906495017 Functional Loss SNV dbSNP153 33..33 33 - - - 91445 RMVar_ID_91445 Human_SNP_ID_488605517 m1A Human chr12 - 3010953 3010953 3010953 CCTCTCAGTGGAGAGAAGGACAAAAGGCTGGAAGCAGTGAGGGGGTGCGGGGTACCTTCTGCGGA CCTCTCAGTGGAGAGAAGGACAAAAGGCTGGAGGCAGTGAGGGGGTGCGGGGTACCTTCTGCGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:3010950..3011117 26863196 MeRIP-seq:(Medium) rs111630436 Functional Loss SNV dbSNP153 33..33 33 - - - 91446 RMVar_ID_91446 Human_SNP_ID_488613438 m1A Human chr12 - 3040476 3040476 3040476 CTCTTCCCCCCTCCCTGCTCCCCGAGTCTCTCATTCTTTCACCAGCCTGTAGATGTGGTGCTGAG CTCTTCCCCCCTCCCTGCTCCCCGAGTCTCTCTTTCTTTCACCAGCCTGTAGATGTGGTGCTGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:3040426..3040601 26863196 MeRIP-seq:(Medium) rs754035071 Functional Loss SNV dbSNP153 33..33 33 - - - 91447 RMVar_ID_91447 Human_SNP_ID_488613439 m1A Human chr12 - 3040476 3040476 3040476 CTCTTCCCCCCTCCCTGCTCCCCGAGTCTCTCATTCTTTCACCAGCCTGTAGATGTGGTGCTGAG CTCTTCCCCCCTCCCTGCTCCCCGAGTCTCTCGTTCTTTCACCAGCCTGTAGATGTGGTGCTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:3040426..3040601 26863196 MeRIP-seq:(Medium) rs754035071 Functional Loss SNV dbSNP153 33..33 33 - - - 91448 RMVar_ID_91448 Human_SNP_ID_488614311 m1A Human chr12 + 3043500 3043500 3043500 AATGTGGCAGTGGGGATGTGGCAGTGAGGAAGACGACAGACAGGCTCCTTGGGAAGCAGAGTAAG AATGTGGCAGTGGGGATGTGGCAGTGAGGAAGTCGACAGACAGGCTCCTTGGGAAGCAGAGTAAG A T AC125807.2 Ensembl:ENSG00000250899 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:3043451..3043997 26863196 MeRIP-seq:(Medium) rs969225835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5557085,Human_RBP_ID_8179991 91449 RMVar_ID_91449 Human_SNP_ID_488614319 m1A Human chr12 + 3043535 3043535 3043535 ACAGACAGGCTCCTTGGGAAGCAGAGTAAGCAAGTGAGGAGACAGGCGGGCGTGGTGAGGCTGCG ACAGACAGGCTCCTTGGGAAGCAGAGTAAGCAGGTGAGGAGACAGGCGGGCGTGGTGAGGCTGCG A G AC125807.2 Ensembl:ENSG00000250899 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:3043485..3043751 26863196 MeRIP-seq:(Medium) rs1471667828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8179991 91450 RMVar_ID_91450 Human_SNP_ID_488622224 m1A Human chr12 + 3071676 3071675 3071676 GGATCTTGGCCTTCTCCTTCCTCTTCTCCTCCAGGGTGGCTGTCACTGCCTGGTACTTCCAGCCA GGATCTTGGCCTTCTCCTTCCTCTTCTCCTCC_GGGTGGCTGTCACTGCCTGGTACTTCCAGCCA CA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:3071579..3071682 26863410 MeRIP-seq:(Medium) rs1274280233 Functional Loss DEL dbSNP153 33..33 33 - - - 91451 RMVar_ID_91451 Human_SNP_ID_488622226 m1A Human chr12 + 3071676 3071676 3071676 GGATCTTGGCCTTCTCCTTCCTCTTCTCCTCCAGGGTGGCTGTCACTGCCTGGTACTTCCAGCCA GGATCTTGGCCTTCTCCTTCCTCTTCTCCTCCGGGGTGGCTGTCACTGCCTGGTACTTCCAGCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:3071579..3071682 26863410 MeRIP-seq:(Medium) rs754199079 Functional Loss SNV dbSNP153 33..33 33 - - - 91452 RMVar_ID_91452 Human_SNP_ID_488660089 m1A Human chr12 - 3211860 3211860 3211860 ATCCCTCTCCAGAAGAGGAGAAGAGGAAACACAAGAAGAAACGCCTGGTGCAGAGCCCCAATTCC ATCCCTCTCCAGAAGAGGAGAAGAGGAAACACGAGAAGAAACGCCTGGTGCAGAGCCCCAATTCC T C AC005912.1 Ensembl:ENSG00000227081 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1222103063 Functional Loss SNV dbSNP153 33..33 33 - - - 91453 RMVar_ID_91453 Human_SNP_ID_488930521 m1A Human chr12 - 4321282 4321282 4321282 GCCATACTCACTGCCGGACAACAGTCAGAGCGAAGCGAGCCATGTTCCCGGAGCCGCGTCCCGTC GCCATACTCACTGCCGGACAACAGTCAGAGCGGAGCGAGCCATGTTCCCGGAGCCGCGTCCCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:4321178..4321340 26863196 MeRIP-seq:(Medium) rs1249784040 Functional Loss SNV dbSNP153 33..33 33 - - - 91454 RMVar_ID_91454 Human_SNP_ID_488933099 m1A Human chr12 + 4331239 4331239 4331239 TTGCTCATTTTTTTCCTCCTCTCAAAAACAGTATAATTTGGCTAATAAGGTTGTCCTTCTCTTTC TTGCTCATTTTTTTCCTCCTCTCAAAAACAGTGTAATTTGGCTAATAAGGTTGTCCTTCTCTTTC A G TIGAR,AC008012.1 Ensembl:ENSG00000078237,Ensembl:ENSG00000285901 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:4331236..4331366 26863196 MeRIP-seq:(Medium) rs368097902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1325853,Human_Splice_Rec_1325869,Human_Splice_Rec_1325879 RMVar_hsa_circ_117086,RMVar_hsa_circ_154392 91455 RMVar_ID_91455 Human_SNP_ID_488998514 m1A Human chr12 - 4605024 4605024 4605024 ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTACAACTCCGCCGTGATGCAGCCCAGGCTCCACA ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTGCAACTCCGCCGTGATGCAGCCCAGGCTCCACA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:4604914..4605076 26863196 MeRIP-seq:(Medium) rs750221184 Functional Loss SNV dbSNP153 33..33 33 - - - 91456 RMVar_ID_91456 Human_SNP_ID_488998515 m1A Human chr12 - 4605024 4605024 4605024 ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTACAACTCCGCCGTGATGCAGCCCAGGCTCCACA ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTCCAACTCCGCCGTGATGCAGCCCAGGCTCCACA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:4604914..4605076 26863196 MeRIP-seq:(Medium) rs750221184 Functional Loss SNV dbSNP153 33..33 33 - - - 91457 RMVar_ID_91457 Human_SNP_ID_489011186 m1A Human chr12 + 4657808 4657808 4657808 TCCGACGAGTAGTACAACACAGCAATGTGGTCATCAATCTTATTGGACGAGACTGGGAAACCAAG TCCGACGAGTAGTACAACACAGCAATGTGGTCCTCAATCTTATTGGACGAGACTGGGAAACCAAG A C AC005833.1,AC005832.4,NDUFA9 Ensembl:ENSG00000255639,Ensembl:ENSG00000272921,Ensembl:ENSG00000139180 Protein coding,Protein coding,Protein coding CDS,3'UTR,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:4657732..4659077 32194978 MeRIP-seq:(Medium) rs1353904541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992304,Human_RBP_ID_1795439,Human_RBP_ID_3406256,Human_RBP_ID_4222811 Human_Splice_Rec_1326358,Human_Splice_Rec_1326359,Human_Splice_Rec_1326402,Human_Splice_Rec_1326403,Human_Splice_Rec_1326414,Human_Splice_Rec_1326415,Human_Splice_Rec_1326440,Human_Splice_Rec_1326441,Human_Splice_Rec_1326458,Human_Splice_Rec_1326459,Human_Splice_Rec_1326465,Human_Splice_Rec_1326480,Human_Splice_Rec_1326481,Human_Splice_Rec_1326503 RMVar_hsa_circ_5001,RMVar_hsa_circ_281527,RMVar_hsa_circ_333135,RMVar_hsa_circ_323264,RMVar_hsa_circ_102194,RMVar_hsa_circ_154400,RMVar_hsa_circ_4708,RMVar_hsa_circ_154401,RMVar_hsa_circ_154399,RMVar_hsa_circ_47965,RMVar_hsa_circ_298277,RMVar_hsa_circ_365875,RMVar_hsa_circ_154402 91458 RMVar_ID_91458 Human_SNP_ID_489233898 m1A Human chr12 - 5572182 5572182 5572182 GCTGAAAGAAAAAAACAAACTCCATATTAAGGAGAGGATGCTGGTCCTGTTGAGGTGCGTGGAGT GCTGAAAGAAAAAAACAAACTCCATATTAAGGGGAGGATGCTGGTCCTGTTGAGGTGCGTGGAGT T C ANO2 Ensembl:ENSG00000047617 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5572161..5572292 26863196 MeRIP-seq:(Medium) rs867002851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154415 91459 RMVar_ID_91459 Human_SNP_ID_489234498 m1A Human chr12 - 5575126 5575120 5575127 AGAGGGAGATTACTTGAGGGACTAGAATGGAAAGGGTGGGCCTCCTGGAGGGGCAGCTAGGTGTT AGAGGGAGATTACTTGAGGGACTAGAATGGA_______GGCCTCCTGGAGGGGCAGCTAGGTGTT CCACCCTT C ANO2 Ensembl:ENSG00000047617 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5575090..5575183 26863196 MeRIP-seq:(Medium) rs1324346156 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_154415 91460 RMVar_ID_91460 Human_SNP_ID_489266510 m1A Human chr12 + 5706350 5706350 5706350 TCCAGCTGCCTCTCAGATCTCATCCCCTCCCCACTCCCTTTTGCTCTTTCCCATCCTGTCACACT TCCAGCTGCCTCTCAGATCTCATCCCCTCCCCGCTCCCTTTTGCTCTTTCCCATCCTGTCACACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:5706299..5706531 26863196 MeRIP-seq:(Medium) rs7977488 Functional Loss SNV dbSNP153 33..33 33 - - - 91461 RMVar_ID_91461 Human_SNP_ID_489274627 m1A Human chr12 - 5740928 5740928 5740928 GGATGAGGGTAGAAGCTGGAGGATAGCACAGGAGAGAGGGACAACGTGCGCAAGTCGAGTATGGA GGATGAGGGTAGAAGCTGGAGGATAGCACAGGGGAGAGGGACAACGTGCGCAAGTCGAGTATGGA T C ANO2 Ensembl:ENSG00000047617 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:5740886..5741020 26863196 MeRIP-seq:(Medium) rs140023940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1327135,Human_Splice_Rec_1327145 RMVar_hsa_circ_53655,RMVar_hsa_circ_87189,RMVar_hsa_circ_154418,RMVar_hsa_circ_357474,RMVar_hsa_circ_66965,RMVar_hsa_circ_356116,RMVar_hsa_circ_363425,RMVar_hsa_circ_365380,RMVar_hsa_circ_351764,RMVar_hsa_circ_353463,RMVar_hsa_circ_335399,RMVar_hsa_circ_115364,RMVar_hsa_circ_116180,RMVar_hsa_circ_112568,RMVar_hsa_circ_98114,RMVar_hsa_circ_101876,RMVar_hsa_circ_88529,RMVar_hsa_circ_154421,RMVar_hsa_circ_154423,RMVar_hsa_circ_154425,RMVar_hsa_circ_154426,RMVar_hsa_circ_154424,RMVar_hsa_circ_154422,RMVar_hsa_circ_154420 91462 RMVar_ID_91462 Human_SNP_ID_489286900 m1A Human chr12 + 5796165 5796165 5796165 ACACTCACACACACACAGTCACACAATCGCTCATTCATACACACTCATGCACACACTCTCTCACA ACACTCACACACACACAGTCACACAATCGCTCTTTCATACACACTCATGCACACACTCTCTCACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5796141..5796582 26863196 MeRIP-seq:(Medium) rs1293882310 Functional Loss SNV dbSNP153 33..33 33 - - - 91463 RMVar_ID_91463 Human_SNP_ID_489309387 m1A Human chr12 - 5888089 5888089 5888089 CACATCCGAACGTCAGAAGGAACAGACTCCGGACACCCCGCCTTTAAGAACTGTAACACTCACTG CACATCCGAACGTCAGAAGGAACAGACTCCGGGCACCCCGCCTTTAAGAACTGTAACACTCACTG T C ANO2 Ensembl:ENSG00000047617 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:5888067..5888151 26863196 MeRIP-seq:(Medium) rs567821989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_363675 91464 RMVar_ID_91464 Human_SNP_ID_489317617 m1A Human chr12 - 5921113 5921111 5921114 TGAGCTGGGACCGCTCGATGCCCTGGAGGAGGAGAGGAAGGAGCAGCGGGAGGAATTTGAGCACA TGAGCTGGGACCGCTCGATGCCCTGGAGGAG___AGGAAGGAGCAGCGGGAGGAATTTGAGCACA TCTC T ANO2 Ensembl:ENSG00000047617 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:5921062..5921180 26863196 MeRIP-seq:(Medium) rs763816588 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1326927,Human_Splice_Rec_1326969,Human_Splice_Rec_1327019,Human_Splice_Rec_1327069 RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_126802,RMVar_hsa_circ_363675,RMVar_hsa_circ_320262,RMVar_hsa_circ_154431,RMVar_hsa_circ_78556,RMVar_hsa_circ_154430 91465 RMVar_ID_91465 Human_SNP_ID_489317634 m1A Human chr12 - 5921136 5921136 5921136 CATGCTGGGGGCCCAGGTGACATTGAGCTGGGACCGCTCGATGCCCTGGAGGAGGAGAGGAAGGA CATGCTGGGGGCCCAGGTGACATTGAGCTGGGGCCGCTCGATGCCCTGGAGGAGGAGAGGAAGGA T C ANO2 Ensembl:ENSG00000047617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5921087..5921177 26863196 MeRIP-seq:(Medium) rs3741902 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1326927,Human_Splice_Rec_1326969,Human_Splice_Rec_1327019,Human_Splice_Rec_1327069 GWAS_ID_11832,GWAS_ID_11833,GWAS_ID_11834,GWAS_ID_11835,GWAS_ID_11836,GWAS_ID_11837,GWAS_ID_11838,GWAS_ID_11839,GWAS_ID_11840,GWAS_ID_11841,GWAS_ID_11842,GWAS_ID_11843,GWAS_ID_11844,GWAS_ID_11845,GWAS_ID_11846,GWAS_ID_11847,GWAS_ID_11848,GWAS_ID_11849,GWAS_ID_11850,GWAS_ID_11851,GWAS_ID_11852,GWAS_ID_11853,GWAS_ID_11854,GWAS_ID_11855,GWAS_ID_11856,GWAS_ID_11857 RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_126802,RMVar_hsa_circ_363675,RMVar_hsa_circ_320262,RMVar_hsa_circ_154431,RMVar_hsa_circ_78556,RMVar_hsa_circ_154430 91466 RMVar_ID_91466 Human_SNP_ID_489318198 m1A Human chr12 - 5922711 5922711 5922711 CCAGGGCCCCAAACATGGACAGCAGTGTCTCAAGATGCCAGGTCCCCGGGCCCCAGGTCTGCAGG CCAGGGCCCCAAACATGGACAGCAGTGTCTCAGGATGCCAGGTCCCCGGGCCCCAGGTCTGCAGG T C ANO2 Ensembl:ENSG00000047617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5922660..5922751 26863196 MeRIP-seq:(Medium) rs779917319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1326924,Human_Splice_Rec_1326925,Human_Splice_Rec_1326966,Human_Splice_Rec_1326967,Human_Splice_Rec_1327016,Human_Splice_Rec_1327017,Human_Splice_Rec_1327066,Human_Splice_Rec_1327067 RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_126802,RMVar_hsa_circ_363675,RMVar_hsa_circ_320262,RMVar_hsa_circ_154431,RMVar_hsa_circ_78556,RMVar_hsa_circ_154430 91467 RMVar_ID_91467 Human_SNP_ID_489401556 m1A Human chr12 + 6220025 6220025 6220025 AAAAGAATGACTCAGAGGTCCCCTGGACCTCAAGGAGCTTGTGCTCTGCTGAGATGGGAGGCAAA AAAAGAATGACTCAGAGGTCCCCTGGACCTCAGGGAGCTTGTGCTCTGCTGAGATGGGAGGCAAA A G CD9 Ensembl:ENSG00000010278 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6220020..6220194 26863196 MeRIP-seq:(Medium) rs532343026 Functional Loss SNV dbSNP153 33..33 33 - - - 91468 RMVar_ID_91468 Human_SNP_ID_489432816 m1A Human chr12 - 6334164 6334164 6334164 CTGGTCCCTCACCTAGGGGACAGGGAGAAGAGAGATAGTGTGTGTCCCCAAGGAAAATATATCCA CTGGTCCCTCACCTAGGGGACAGGGAGAAGAGGGATAGTGTGTGTCCCCAAGGAAAATATATCCA T C TNFRSF1A Ensembl:ENSG00000067182 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6334042..6334262 26863196 MeRIP-seq:(Medium) rs878905246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33296,Human_RBP_ID_4236365,Human_RBP_ID_19703716,Human_RBP_ID_22436795,Human_RBP_ID_23569351,Human_RBP_ID_24364821 Human_Splice_Rec_1327644,Human_Splice_Rec_1327645,Human_Splice_Rec_1327670,Human_Splice_Rec_1327671,Human_Splice_Rec_1327686,Human_Splice_Rec_1327687,Human_Splice_Rec_1327722,Human_Splice_Rec_1327723,Human_Splice_Rec_1327734,Human_Splice_Rec_1327735,Human_Splice_Rec_1327743,Human_Splice_Rec_1327752,Human_Splice_Rec_1327753,Human_Splice_Rec_1327760,Human_Splice_Rec_1327761,Human_Splice_Rec_1327766,Human_Splice_Rec_1327767,Human_Splice_Rec_1327772,Human_Splice_Rec_1327773,Human_Splice_Rec_1327776 RMVar_hsa_circ_24377,RMVar_hsa_circ_126548,RMVar_hsa_circ_154481,RMVar_hsa_circ_272107,RMVar_hsa_circ_154484 91469 RMVar_ID_91469 Human_SNP_ID_489433989 m1A Human chr12 - 6339071 6339067 6339071 GAGAAACACTAAGAAATGTGAATGGGAGAATTAGAGGGAGTGGGGGAGAGGATGGAGGAAGAGTG GAGAAACACTAAGAAATGTGAATGGGAGAATT____GGAGTGGGGGAGAGGATGGAGGAAGAGTG CCTCT C TNFRSF1A Ensembl:ENSG00000067182 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6339066..6339280 26863196 MeRIP-seq:(Medium) rs554811271 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23569366 91470 RMVar_ID_91470 Human_SNP_ID_489444522 m1A Human chr12 + 6375751 6375751 6375751 CTTTAGACGCAGACAGGCAAGGAGGCTGGGGGACAGGATGGCAGGTGAGGGGCAAAGATCTGAAC CTTTAGACGCAGACAGGCAAGGAGGCTGGGGGGCAGGATGGCAGGTGAGGGGCAAAGATCTGAAC A G LTBR Ensembl:ENSG00000111321 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6375568..6376025 26863196 MeRIP-seq:(Medium) rs1447498429 Functional Loss SNV dbSNP153 33..33 33 - - - 91471 RMVar_ID_91471 Human_SNP_ID_489446703 m1A Human chr12 - 6384215 6384215 6384215 GACTCAGGGCCGATGTGCACCCCAGGGCCGGGAGCGGCCAGGCCGGGCCTCCAGGGCTCCCATGG GACTCAGGGCCGATGTGCACCCCAGGGCCGGGGGCGGCCAGGCCGGGCCTCCAGGGCTCCCATGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6384166..6384325 26863196 MeRIP-seq:(Medium) rs901487838 Functional Loss SNV dbSNP153 33..33 33 - - - 91472 RMVar_ID_91472 Human_SNP_ID_489448262 m1A Human chr12 + 6389218 6389217 6389218 GAGCGGAGAGCTGAAGAAGCAAGGAGCCAGCCATGGGGTTATCTGGGGAGAAAGTGCTCCAGGAA GAGCGGAGAGCTGAAGAAGCAAGGAGCCAGCC_TGGGGTTATCTGGGGAGAAAGTGCTCCAGGAA CA C LTBR Ensembl:ENSG00000111321 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6389213..6389365 26863196 MeRIP-seq:(Medium) rs869066282 Functional Loss DEL dbSNP153 33..33 33 - - - 91473 RMVar_ID_91473 Human_SNP_ID_489448263 m1A Human chr12 + 6389218 6389218 6389218 GAGCGGAGAGCTGAAGAAGCAAGGAGCCAGCCATGGGGTTATCTGGGGAGAAAGTGCTCCAGGAA GAGCGGAGAGCTGAAGAAGCAAGGAGCCAGCCCTGGGGTTATCTGGGGAGAAAGTGCTCCAGGAA A C LTBR Ensembl:ENSG00000111321 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6389213..6389365 26863196 MeRIP-seq:(Medium) rs1555117766 Functional Loss SNV dbSNP153 33..33 33 - - - 91474 RMVar_ID_91474 Human_SNP_ID_489448943 m1A Human chr12 + 6391494 6391494 6391494 GGGGTTGGGTAGGATTCCTAGGTATGGGGAAGAGTTTTGGAAGGGGAGGAAAATGGCAAGTGTAT GGGGTTGGGTAGGATTCCTAGGTATGGGGAAGGGTTTTGGAAGGGGAGGAAAATGGCAAGTGTAT A G LTBR Ensembl:ENSG00000111321 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6391444..6391512 26863196 MeRIP-seq:(Medium) rs985792913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36513,Human_RBP_ID_5139534,Human_RBP_ID_8178421,Human_RBP_ID_18934228,Human_RBP_ID_21884436,Human_RBP_ID_26420976 Human_miRNA_ID_238734,Human_miRNA_ID_1730285 91475 RMVar_ID_91475 Human_SNP_ID_489476101 m1A Human chr12 - 6492452 6492452 6492452 TCTCTCACATTACACAGGAAACTTTGAAAAGCACCCCAAAGAACTGATCAGGGGGCCCATATGGC TCTCTCACATTACACAGGAAACTTTGAAAAGCCCCCCAAAGAACTGATCAGGGGGCCCATATGGC T G MRPL51 Ensembl:ENSG00000111639 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6492318..6492486 26863196 MeRIP-seq:(Medium) rs753429240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364532,Human_RBP_ID_17650300,Human_RBP_ID_26321108 Human_Splice_Rec_1328360,Human_Splice_Rec_1328362,Human_Splice_Rec_1328366,Human_Splice_Rec_1328368,Human_Splice_Rec_1328372,Human_Splice_Rec_1328376 RMVar_hsa_circ_84896,RMVar_hsa_circ_128080,RMVar_hsa_circ_154500,RMVar_hsa_circ_154501 91476 RMVar_ID_91476 Human_SNP_ID_489476259 m1A Human chr12 + 6492939 6492939 6492939 CGTTCCAACGATCAACCACTTTGGGGGGCGGGAGAGTGAGCCTTATACCGATCAATCTAGGCACA CGTTCCAACGATCAACCACTTTGGGGGGCGGGGGAGTGAGCCTTATACCGATCAATCTAGGCACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6492272..6492958 32194978 MeRIP-seq:(Medium) rs746799618 Functional Loss SNV dbSNP153 33..33 33 - - - 91477 RMVar_ID_91477 Human_SNP_ID_489476260 m1A Human chr12 + 6492939 6492939 6492939 CGTTCCAACGATCAACCACTTTGGGGGGCGGGAGAGTGAGCCTTATACCGATCAATCTAGGCACA CGTTCCAACGATCAACCACTTTGGGGGGCGGGTGAGTGAGCCTTATACCGATCAATCTAGGCACA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6492272..6492958 32194978 MeRIP-seq:(Medium) rs746799618 Functional Loss SNV dbSNP153 33..33 33 - - - 91478 RMVar_ID_91478 Human_SNP_ID_489476354 m1A Human chr12 + 6493179 6493179 6493179 TCCCCCCTTCAACAGCACACCAAATAAGCCCAAGAAGATGACAGGAACCGTCCCCGCCAACTTCA TCCCCCCTTCAACAGCACACCAAATAAGCCCAGGAAGATGACAGGAACCGTCCCCGCCAACTTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6493043..6493300 26863196 MeRIP-seq:(Medium) rs773130350 Functional Loss SNV dbSNP153 33..33 33 - - - 91479 RMVar_ID_91479 Human_SNP_ID_489476366 m1A Human chr12 - 6493197 6493197 6493197 TTCGCCTTAGTACTCGTGTGAAGTTGGCGGGGACGGTTCCTGTCATCTTCTTGGGCTTATTTGGT TTCGCCTTAGTACTCGTGTGAAGTTGGCGGGGGCGGTTCCTGTCATCTTCTTGGGCTTATTTGGT T C MRPL51 Ensembl:ENSG00000111639 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:6492842..6493275;chr12:6492952..6493300 26863196 MeRIP-seq:(Medium) rs1565536256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246471,Human_RBP_ID_5235399,Human_RBP_ID_5462064,Human_RBP_ID_9322405,Human_RBP_ID_17824750,Human_RBP_ID_22436799,Human_RBP_ID_23125808,Human_RBP_ID_23207519,Human_RBP_ID_23570219,Human_RBP_ID_26423916 Human_miRNA_ID_3088404 RMVar_hsa_circ_128080,RMVar_hsa_circ_154501 91480 RMVar_ID_91480 Human_SNP_ID_489476720 m1A Human chr12 + 6494153 6494153 6494153 CTGCCGGAATCAGAGCCGCGGGTGAGATCCCCAGGTAAGATGTGGTGTTGCAGGTCGTAAAAGAG CTGCCGGAATCAGAGCCGCGGGTGAGATCCCCGGGTAAGATGTGGTGTTGCAGGTCGTAAAAGAG A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:6494051..6494199;chr12:6494061..6494193;chr12:6494054..6494215;chr12:6494053..6494202 26863196 MeRIP-seq:(Medium) rs966470444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755341,Human_RBP_ID_1065432,Human_RBP_ID_4247226,Human_RBP_ID_22572096,Human_RBP_ID_24557610,Human_RBP_ID_25015215 Human_Splice_Rec_1328386,Human_Splice_Rec_1328387,Human_Splice_Rec_1328397,Human_Splice_Rec_1328437,Human_Splice_Rec_1328497 RMVar_hsa_circ_364055 91481 RMVar_ID_91481 Human_SNP_ID_489476953 m1A Human chr12 - 6495043 6495043 6495043 CTAGAAACCAAACAGTGAAAAAGTCAGGGTCTATATTCAAGACCTGTCTTCGTATCTGGTTCTAT CTAGAAACCAAACAGTGAAAAAGTCAGGGTCTGTATTCAAGACCTGTCTTCGTATCTGGTTCTAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6495041..6495250 26863196 MeRIP-seq:(Medium) rs1483467999 Functional Loss SNV dbSNP153 33..33 33 - - - 91482 RMVar_ID_91482 Human_SNP_ID_489476955 m1A Human chr12 + 6495060 6495060 6495060 GACAGGTCTTGAATATAGACCCTGACTTTTTCACTGTTTGGTTTCTAGCCCTGTGAGCCTGTAGG GACAGGTCTTGAATATAGACCCTGACTTTTTCTCTGTTTGGTTTCTAGCCCTGTGAGCCTGTAGG A T NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6495057..6495225 26863196 MeRIP-seq:(Medium) rs1406985598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12008521 RMVar_hsa_circ_364055 91483 RMVar_ID_91483 Human_SNP_ID_489482322 m1A Human chr12 - 6514258 6514258 6514258 GGCGGTAGCAACAGCCAGTAACCAAACTGAGAAAGGAAGAGTTTGAGATGATGAAAGCAGCTGTC GGCGGTAGCAACAGCCAGTAACCAAACTGAGACAGGAAGAGTTTGAGATGATGAAAGCAGCTGTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6514251..6514400 32194978 MeRIP-seq:(Medium) rs768527337 Functional Loss SNV dbSNP153 33..33 33 - - - 91484 RMVar_ID_91484 Human_SNP_ID_489482435 m1A Human chr12 - 6514569 6514569 6514569 GAAGGAAGAGTCACCTTACAATCTCTCCCACTATGCTCTTCATTCCATAGTCAGTTGCCCATAGA GAAGGAAGAGTCACCTTACAATCTCTCCCACTGTGCTCTTCATTCCATAGTCAGTTGCCCATAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6514519..6514608 26863196 MeRIP-seq:(Medium) rs1257145371 Functional Loss SNV dbSNP153 33..33 33 - - - 91485 RMVar_ID_91485 Human_SNP_ID_489484947 m1A Human chr12 + 6522975 6522975 6522975 GGAAGCCGTGCTTAATGCCTACCGCCAACTCTACCTCAACCCCAAAGGGGACTCTGCCAGGTATA GGAAGCCGTGCTTAATGCCTACCGCCAACTCTGCCTCAACCCCAAAGGGGACTCTGCCAGGTATA A G NCAPD2 Ensembl:ENSG00000010292 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6522951..6522975 32194978 MeRIP-seq:(Medium) rs765390473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425870,Human_RBP_ID_752763,Human_RBP_ID_8784345,Human_RBP_ID_9255293,Human_RBP_ID_9278386,Human_RBP_ID_17240112,Human_RBP_ID_17355668,Human_RBP_ID_17473035,Human_RBP_ID_18188661,Human_RBP_ID_18631516,Human_RBP_ID_27424429 Human_Splice_Rec_1328421,Human_Splice_Rec_1328465,Human_Splice_Rec_1328527,Human_Splice_Rec_1328574,Human_Splice_Rec_1328575 Human_miRNA_ID_1914456,Human_miRNA_ID_1916908,Human_miRNA_ID_1919358,Human_miRNA_ID_1921815,Human_miRNA_ID_1924271,Human_miRNA_ID_1926721,Human_miRNA_ID_1929172,Human_miRNA_ID_1931626,Human_miRNA_ID_2629453,Human_miRNA_ID_2642564,Human_miRNA_ID_3125307 RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_117656,RMVar_hsa_circ_154511,RMVar_hsa_circ_154517,RMVar_hsa_circ_371401,RMVar_hsa_circ_332251,RMVar_hsa_circ_76078,RMVar_hsa_circ_103761,RMVar_hsa_circ_30144,RMVar_hsa_circ_123765,RMVar_hsa_circ_154519,RMVar_hsa_circ_154520,RMVar_hsa_circ_112971,RMVar_hsa_circ_120363,RMVar_hsa_circ_154521,RMVar_hsa_circ_103652,RMVar_hsa_circ_154522,RMVar_hsa_circ_285837,RMVar_hsa_circ_123089,RMVar_hsa_circ_112593,RMVar_hsa_circ_154524,RMVar_hsa_circ_154526,RMVar_hsa_circ_154527,RMVar_hsa_circ_154528,RMVar_hsa_circ_154525,RMVar_hsa_circ_339458 91486 RMVar_ID_91486 Human_SNP_ID_489484948 m1A Human chr12 + 6522975 6522975 6522975 GGAAGCCGTGCTTAATGCCTACCGCCAACTCTACCTCAACCCCAAAGGGGACTCTGCCAGGTATA GGAAGCCGTGCTTAATGCCTACCGCCAACTCTTCCTCAACCCCAAAGGGGACTCTGCCAGGTATA A T NCAPD2 Ensembl:ENSG00000010292 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6522951..6522975 32194978 MeRIP-seq:(Medium) rs765390473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425870,Human_RBP_ID_752763,Human_RBP_ID_8784345,Human_RBP_ID_9255293,Human_RBP_ID_9278386,Human_RBP_ID_17240112,Human_RBP_ID_17355668,Human_RBP_ID_17473035,Human_RBP_ID_18188661,Human_RBP_ID_18631516,Human_RBP_ID_27424429 Human_Splice_Rec_1328421,Human_Splice_Rec_1328465,Human_Splice_Rec_1328527,Human_Splice_Rec_1328574,Human_Splice_Rec_1328575 Human_miRNA_ID_1914456,Human_miRNA_ID_1916908,Human_miRNA_ID_1919358,Human_miRNA_ID_1921815,Human_miRNA_ID_1924271,Human_miRNA_ID_1926721,Human_miRNA_ID_1929172,Human_miRNA_ID_1931626,Human_miRNA_ID_2629453,Human_miRNA_ID_2642564,Human_miRNA_ID_3125307 RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_117656,RMVar_hsa_circ_154511,RMVar_hsa_circ_154517,RMVar_hsa_circ_371401,RMVar_hsa_circ_332251,RMVar_hsa_circ_76078,RMVar_hsa_circ_103761,RMVar_hsa_circ_30144,RMVar_hsa_circ_123765,RMVar_hsa_circ_154519,RMVar_hsa_circ_154520,RMVar_hsa_circ_112971,RMVar_hsa_circ_120363,RMVar_hsa_circ_154521,RMVar_hsa_circ_103652,RMVar_hsa_circ_154522,RMVar_hsa_circ_285837,RMVar_hsa_circ_123089,RMVar_hsa_circ_112593,RMVar_hsa_circ_154524,RMVar_hsa_circ_154526,RMVar_hsa_circ_154527,RMVar_hsa_circ_154528,RMVar_hsa_circ_154525,RMVar_hsa_circ_339458 91487 RMVar_ID_91487 Human_SNP_ID_489486385 m1A Human chr12 - 6527820 6527820 6527820 GTTCTGCCTCTGTGTCATCTGCTGTTGCCCCAACCAGCCCCAGCTCCTCCTCCATGGTGGTCTCA GTTCTGCCTCTGTGTCATCTGCTGTTGCCCCAGCCAGCCCCAGCTCCTCCTCCATGGTGGTCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6527753..6527872 26863196 MeRIP-seq:(Medium) rs774202915 Functional Loss SNV dbSNP153 33..33 33 - - - 91488 RMVar_ID_91488 Human_SNP_ID_489486555 m1A Human chr12 + 6528292 6528292 6528292 TGCCACTGGGGATCTGGCCATCCGCTTTCCCAATCTGGTGGACCCCTGGACTCCTCATCTGTATG TGCCACTGGGGATCTGGCCATCCGCTTTCCCAGTCTGGTGGACCCCTGGACTCCTCATCTGTATG A G NCAPD2 Ensembl:ENSG00000010292 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6528242..6528330 26863196 MeRIP-seq:(Medium) rs757688351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065433,Human_RBP_ID_1167974,Human_RBP_ID_3411506,Human_RBP_ID_17473105,Human_RBP_ID_18188668,Human_RBP_ID_18631543 Human_Splice_Rec_1328483,Human_Splice_Rec_1328545 RMVar_hsa_circ_37618,RMVar_hsa_circ_76078,RMVar_hsa_circ_103761,RMVar_hsa_circ_154521,RMVar_hsa_circ_154528,RMVar_hsa_circ_127039,RMVar_hsa_circ_154531,RMVar_hsa_circ_86107,RMVar_hsa_circ_154533,RMVar_hsa_circ_80445,RMVar_hsa_circ_154535,RMVar_hsa_circ_68013,RMVar_hsa_circ_324524 91489 RMVar_ID_91489 Human_SNP_ID_489486690 m1A Human chr12 - 6528726 6528726 6528726 CCTTCACCATGTCCTTGAGGATCAGGTGGGTCATCACCAGCCCCGCTGTTTTCCGCACTTGCTGA CCTTCACCATGTCCTTGAGGATCAGGTGGGTCGTCACCAGCCCCGCTGTTTTCCGCACTTGCTGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6528676..6528750 32194978 MeRIP-seq:(Medium) rs144412706 Functional Loss SNV dbSNP153 33..33 33 - - - 91490 RMVar_ID_91490 Human_SNP_ID_489487421 m1A Human chr12 + 6531014 6531014 6531014 CCGCCGTACTACCCGTCGGCATCCAAACACCCAGCAGCGAGCTTCCAAAAAGAAACCCAAAGTTG CCGCCGTACTACCCGTCGGCATCCAAACACCCGGCAGCGAGCTTCCAAAAAGAAACCCAAAGTTG A G NCAPD2 Ensembl:ENSG00000010292 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6530965..6531040 26863196 MeRIP-seq:(Medium) rs1031646703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275547,Human_RBP_ID_22912625,Human_RBP_ID_27424433 Human_Splice_Rec_1328494,Human_Splice_Rec_1328495,Human_Splice_Rec_1328556,Human_Splice_Rec_1328557 Human_miRNA_ID_1356281 RMVar_hsa_circ_103761,RMVar_hsa_circ_154521,RMVar_hsa_circ_80445,RMVar_hsa_circ_154535 91491 RMVar_ID_91491 Human_SNP_ID_489488559 m1A Human chr12 + 6534568 6534568 6534568 CGACAGTCAGCCGCATCTTCTTTTGCGTCGCCAGGTGAAGACGGGCGGAGAGAAACCCGGGAGGC CGACAGTCAGCCGCATCTTCTTTTGCGTCGCCCGGTGAAGACGGGCGGAGAGAAACCCGGGAGGC A C GAPDH Ensembl:ENSG00000111640 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr12:6534501..6534778;chr12:6534501..6534672 26863196 MeRIP-seq:(Medium) rs1298866363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228761,Human_RBP_ID_425967,Human_RBP_ID_752658,Human_RBP_ID_810932,Human_RBP_ID_877278,Human_RBP_ID_993962,Human_RBP_ID_1167976,Human_RBP_ID_1475979,Human_RBP_ID_4237528,Human_RBP_ID_5170656,Human_RBP_ID_5417496,Human_RBP_ID_5462073,Human_RBP_ID_5492362,Human_RBP_ID_8069040,Human_RBP_ID_8784396,Human_RBP_ID_9278396,Human_RBP_ID_9322409,Human_RBP_ID_17240159,Human_RBP_ID_17356877,Human_RBP_ID_17474668,Human_RBP_ID_18188671,Human_RBP_ID_22176626,Human_RBP_ID_22436195,Human_RBP_ID_26805368 Human_Splice_Rec_1328599,Human_Splice_Rec_1328601,Human_Splice_Rec_1328617,Human_Splice_Rec_1328633,Human_Splice_Rec_1328647,Human_Splice_Rec_1328663 RMVar_hsa_circ_154536,RMVar_hsa_circ_90016,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_154540,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537 91492 RMVar_ID_91492 Human_SNP_ID_489488561 m1A Human chr12 - 6534571 6534571 6534571 CTAGCCTCCCGGGTTTCTCTCCGCCCGTCTTCACCTGGCGACGCAAAAGAAGATGCGGCTGACTG CTAGCCTCCCGGGTTTCTCTCCGCCCGTCTTCGCCTGGCGACGCAAAAGAAGATGCGGCTGACTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:6534526..6534825;chr12:6534526..6534675 26863196 MeRIP-seq:(Medium) rs1342163356 Functional Loss SNV dbSNP153 33..33 33 - - - 91493 RMVar_ID_91493 Human_SNP_ID_489488562 m1A Human chr12 - 6534571 6534571 6534571 CTAGCCTCCCGGGTTTCTCTCCGCCCGTCTTCACCTGGCGACGCAAAAGAAGATGCGGCTGACTG CTAGCCTCCCGGGTTTCTCTCCGCCCGTCTTCCCCTGGCGACGCAAAAGAAGATGCGGCTGACTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:6534526..6534825;chr12:6534526..6534675 26863196 MeRIP-seq:(Medium) rs1342163356 Functional Loss SNV dbSNP153 33..33 33 - - - 91494 RMVar_ID_91494 Human_SNP_ID_489488640 m1A Human chr12 + 6534744 6534739 6534744 GGCGCGGGCTGGGCATGGAGGCCTGGTGGGGGAGGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC GGCGCGGGCTGGGCATGGAGGCCTGGTG_____GGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC GGGGGA G GAPDH Ensembl:ENSG00000111640 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:6534726..6534800 26863196 MeRIP-seq:(Medium) rs1160090025 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_18934231,Human_RBP_ID_21966969,Human_RBP_ID_22645779 RMVar_hsa_circ_154536,RMVar_hsa_circ_90016,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_154540,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537 91495 RMVar_ID_91495 Human_SNP_ID_489488645 m1A Human chr12 + 6534744 6534744 6534744 GGCGCGGGCTGGGCATGGAGGCCTGGTGGGGGAGGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC GGCGCGGGCTGGGCATGGAGGCCTGGTGGGGGGGGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC A G GAPDH Ensembl:ENSG00000111640 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:6534726..6534800 26863196 MeRIP-seq:(Medium) rs1044436316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18934231,Human_RBP_ID_21966969,Human_RBP_ID_22645779 RMVar_hsa_circ_154536,RMVar_hsa_circ_90016,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_154540,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537 91496 RMVar_ID_91496 Human_SNP_ID_489488650 m1A Human chr12 - 6534759 6534759 6534759 CAGTGAGCGCCTAGTGGCCCCGGCCGACACACACGCCTCCCCTCCCCTCCCCCACCAGGCCTCCA CAGTGAGCGCCTAGTGGCCCCGGCCGACACACGCGCCTCCCCTCCCCTCCCCCACCAGGCCTCCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6534751..6534825 26863196 MeRIP-seq:(Medium) rs1466737453 Functional Loss SNV dbSNP153 33..33 33 - - - 91497 RMVar_ID_91497 Human_SNP_ID_489488702 m1A Human chr12 - 6534820 6534820 6534820 CCGACCTTCACCTTCCCCATGGTGTCTGAGCGATGTGGCTCGGCTGCGCGGAGGGAGAGAACAGT CCGACCTTCACCTTCCCCATGGTGTCTGAGCGCTGTGGCTCGGCTGCGCGGAGGGAGAGAACAGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:6534476..6534925;chr12:6534501..6535291;chr12:6534501..6535058 26863196 MeRIP-seq:(Medium) rs1415353727 Functional Loss SNV dbSNP153 33..33 33 - - - 91498 RMVar_ID_91498 Human_SNP_ID_489488726 m1A Human chr12 - 6534863 6534863 6534863 CAGCCCAGGGCCCCCCAGCCACCCGCGAACTCACCCGTTGACTCCGACCTTCACCTTCCCCATGG CAGCCCAGGGCCCCCCAGCCACCCGCGAACTCGCCCGTTGACTCCGACCTTCACCTTCCCCATGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6534801..6534913 32194978 MeRIP-seq:(Medium) rs1468196031 Functional Loss SNV dbSNP153 33..33 33 - - - 91499 RMVar_ID_91499 Human_SNP_ID_489489465 m1A Human chr12 - 6536660 6536660 6536660 CATGTAAACCTGGGGGAATACGTGAGGGTATGAAGGGGCTGCCCATCAGCCAGGTGGCTCCTCCC CATGTAAACCTGGGGGAATACGTGAGGGTATGTAGGGGCTGCCCATCAGCCAGGTGGCTCCTCCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6536651..6536675 26863196 MeRIP-seq:(Medium) rs1189852777 Functional Loss SNV dbSNP153 33..33 33 - - - 91500 RMVar_ID_91500 Human_SNP_ID_489489610 m1A Human chr12 + 6536978 6536978 6536978 GCGATGCTGGCGCTGAGTACGTCGTGGAGTCCACTGGCGTCTTCACCACCATGGAGAAGGCTGGG GCGATGCTGGCGCTGAGTACGTCGTGGAGTCCGCTGGCGTCTTCACCACCATGGAGAAGGCTGGG A G GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6536927..6537069 26863196 MeRIP-seq:(Medium) rs1357480844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425982,Human_RBP_ID_753379,Human_RBP_ID_810935,Human_RBP_ID_1475990,Human_RBP_ID_1799236,Human_RBP_ID_8247799,Human_RBP_ID_9019895,Human_RBP_ID_17240166,Human_RBP_ID_17355703,Human_RBP_ID_18188684,Human_RBP_ID_18631572,Human_RBP_ID_22435746,Human_RBP_ID_27424446 Human_Splice_Rec_1328608,Human_Splice_Rec_1328609,Human_Splice_Rec_1328624,Human_Splice_Rec_1328625,Human_Splice_Rec_1328640,Human_Splice_Rec_1328641,Human_Splice_Rec_1328654,Human_Splice_Rec_1328655,Human_Splice_Rec_1328669,Human_Splice_Rec_1328681,Human_Splice_Rec_1328694,Human_Splice_Rec_1328695,Human_Splice_Rec_1328714,Human_Splice_Rec_1328715,Human_Splice_Rec_1328726,Human_Splice_Rec_1328727 RMVar_hsa_circ_88042,RMVar_hsa_circ_154536,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_105081,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_125986,RMVar_hsa_circ_154542,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_154541,RMVar_hsa_circ_120781,RMVar_hsa_circ_96003,RMVar_hsa_circ_154547,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_154546,RMVar_hsa_circ_120258,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_374391,RMVar_hsa_circ_124027,RMVar_hsa_circ_88412,RMVar_hsa_circ_154552,RMVar_hsa_circ_154554,RMVar_hsa_circ_49293,RMVar_hsa_circ_154553,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551,RMVar_hsa_circ_122873,RMVar_hsa_circ_378260,RMVar_hsa_circ_154556,RMVar_hsa_circ_89669,RMVar_hsa_circ_111060,RMVar_hsa_circ_154558,RMVar_hsa_circ_154559,RMVar_hsa_circ_154560,RMVar_hsa_circ_154557 91501 RMVar_ID_91501 Human_SNP_ID_489489616 m1A Human chr12 + 6536990 6536990 6536990 CTGAGTACGTCGTGGAGTCCACTGGCGTCTTCACCACCATGGAGAAGGCTGGGGTGAGTGCAGGA CTGAGTACGTCGTGGAGTCCACTGGCGTCTTCGCCACCATGGAGAAGGCTGGGGTGAGTGCAGGA A G GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6536928..6537028 32194978 MeRIP-seq:(Medium) rs751350310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34189,Human_RBP_ID_425982,Human_RBP_ID_753379,Human_RBP_ID_810935,Human_RBP_ID_877285,Human_RBP_ID_993964,Human_RBP_ID_1799236,Human_RBP_ID_9019895,Human_RBP_ID_17240166,Human_RBP_ID_17355703,Human_RBP_ID_18188684,Human_RBP_ID_18631572,Human_RBP_ID_22435746,Human_RBP_ID_26805391 Human_Splice_Rec_1328608,Human_Splice_Rec_1328609,Human_Splice_Rec_1328624,Human_Splice_Rec_1328625,Human_Splice_Rec_1328640,Human_Splice_Rec_1328641,Human_Splice_Rec_1328654,Human_Splice_Rec_1328655,Human_Splice_Rec_1328669,Human_Splice_Rec_1328681,Human_Splice_Rec_1328694,Human_Splice_Rec_1328695,Human_Splice_Rec_1328714,Human_Splice_Rec_1328715,Human_Splice_Rec_1328726,Human_Splice_Rec_1328727 RMVar_hsa_circ_88042,RMVar_hsa_circ_154536,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_105081,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_125986,RMVar_hsa_circ_154542,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_154541,RMVar_hsa_circ_120781,RMVar_hsa_circ_96003,RMVar_hsa_circ_154547,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_154546,RMVar_hsa_circ_120258,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_374391,RMVar_hsa_circ_124027,RMVar_hsa_circ_88412,RMVar_hsa_circ_154552,RMVar_hsa_circ_154554,RMVar_hsa_circ_49293,RMVar_hsa_circ_154553,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551,RMVar_hsa_circ_122873,RMVar_hsa_circ_378260,RMVar_hsa_circ_154556,RMVar_hsa_circ_89669,RMVar_hsa_circ_111060,RMVar_hsa_circ_154558,RMVar_hsa_circ_154559,RMVar_hsa_circ_154560,RMVar_hsa_circ_154557 91502 RMVar_ID_91502 Human_SNP_ID_489489625 m1A Human chr12 + 6537003 6537003 6537003 GGAGTCCACTGGCGTCTTCACCACCATGGAGAAGGCTGGGGTGAGTGCAGGAGGGCCCGCGGGAG GGAGTCCACTGGCGTCTTCACCACCATGGAGAGGGCTGGGGTGAGTGCAGGAGGGCCCGCGGGAG A G GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6537001..6537050 32194978 MeRIP-seq:(Medium) rs1361841795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34189,Human_RBP_ID_425982,Human_RBP_ID_877285,Human_RBP_ID_993964,Human_RBP_ID_17240166,Human_RBP_ID_17355703,Human_RBP_ID_18188685,Human_RBP_ID_18631572,Human_RBP_ID_19057490,Human_RBP_ID_22435746,Human_RBP_ID_22755810 Human_Splice_Rec_1328608,Human_Splice_Rec_1328609,Human_Splice_Rec_1328624,Human_Splice_Rec_1328625,Human_Splice_Rec_1328640,Human_Splice_Rec_1328641,Human_Splice_Rec_1328654,Human_Splice_Rec_1328655,Human_Splice_Rec_1328669,Human_Splice_Rec_1328681,Human_Splice_Rec_1328694,Human_Splice_Rec_1328695,Human_Splice_Rec_1328714,Human_Splice_Rec_1328715,Human_Splice_Rec_1328726,Human_Splice_Rec_1328727 RMVar_hsa_circ_88042,RMVar_hsa_circ_154536,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_105081,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_125986,RMVar_hsa_circ_154542,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_154541,RMVar_hsa_circ_120781,RMVar_hsa_circ_96003,RMVar_hsa_circ_154547,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_154546,RMVar_hsa_circ_120258,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_374391,RMVar_hsa_circ_124027,RMVar_hsa_circ_88412,RMVar_hsa_circ_154552,RMVar_hsa_circ_154554,RMVar_hsa_circ_49293,RMVar_hsa_circ_154553,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551,RMVar_hsa_circ_122873,RMVar_hsa_circ_378260,RMVar_hsa_circ_154556,RMVar_hsa_circ_89669,RMVar_hsa_circ_111060,RMVar_hsa_circ_154558,RMVar_hsa_circ_154559,RMVar_hsa_circ_154560,RMVar_hsa_circ_154557 91503 RMVar_ID_91503 Human_SNP_ID_489489947 m1A Human chr12 - 6537686 6537686 6537686 GACCTTGCCCACAGCCTTGGCAGCGCCAGTAGAGGCAGGGATGATGTTCTGGAGAGCCCCGCGGC GACCTTGCCCACAGCCTTGGCAGCGCCAGTAGGGGCAGGGATGATGTTCTGGAGAGCCCCGCGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6537574..6537725 32194978 MeRIP-seq:(Medium) rs11549345 Functional Loss SNV dbSNP153 33..33 33 - - - 91504 RMVar_ID_91504 Human_SNP_ID_489490013 m1A Human chr12 + 6537811 6537811 6537811 TCAGTGGTGGACCTGACCTGCCGTCTAGAAAAACCTGCCAAATATGATGACATCAAGAAGGTGGT TCAGTGGTGGACCTGACCTGCCGTCTAGAAAACCCTGCCAAATATGATGACATCAAGAAGGTGGT A C GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6537573..6537976 26863196 MeRIP-seq:(Medium) rs1062429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269484,Human_RBP_ID_425989,Human_RBP_ID_877292,Human_RBP_ID_1476000,Human_RBP_ID_1799241,Human_RBP_ID_3411539,Human_RBP_ID_4237543,Human_RBP_ID_8381923,Human_RBP_ID_9019900,Human_RBP_ID_12009536,Human_RBP_ID_18631576,Human_RBP_ID_22436822,Human_RBP_ID_22574068,Human_RBP_ID_22795093,Human_RBP_ID_26910373,Human_RBP_ID_27217577 RMVar_hsa_circ_154536,RMVar_hsa_circ_98049,RMVar_hsa_circ_94221,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_96003,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551,RMVar_hsa_circ_122873,RMVar_hsa_circ_111060,RMVar_hsa_circ_154559,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_104707,RMVar_hsa_circ_154562,RMVar_hsa_circ_154563,RMVar_hsa_circ_371552,RMVar_hsa_circ_92138,RMVar_hsa_circ_113434,RMVar_hsa_circ_154565,RMVar_hsa_circ_154566,RMVar_hsa_circ_154568,RMVar_hsa_circ_82776,RMVar_hsa_circ_154567 91505 RMVar_ID_91505 Human_SNP_ID_489490204 m1A Human chr12 + 6538195 6538195 6538195 AGGAGTAAGACCCCTGGACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTG AGGAGTAAGACCCCTGGACCACCAGCCCCAGCGAGAGCACAAGAGGAAGAGAGAGACCCTCACTG A G GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6538155..6538320 26863196 MeRIP-seq:(Medium) rs770280504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426007,Human_RBP_ID_1476008,Human_RBP_ID_1799247,Human_RBP_ID_3411546,Human_RBP_ID_6209879,Human_RBP_ID_12009544,Human_RBP_ID_17240176,Human_RBP_ID_17355709,Human_RBP_ID_17650301,Human_RBP_ID_18188702,Human_RBP_ID_18631586,Human_RBP_ID_22435753,Human_RBP_ID_22532409,Human_RBP_ID_27424469 Human_Splice_Rec_1328616,Human_Splice_Rec_1328632,Human_Splice_Rec_1328662,Human_Splice_Rec_1328676,Human_Splice_Rec_1328688,Human_Splice_Rec_1328702,Human_Splice_Rec_1328708,Human_Splice_Rec_1328722,Human_Splice_Rec_1328734 Human_miRNA_ID_2684866 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 91506 RMVar_ID_91506 Human_SNP_ID_489490205 m1A Human chr12 + 6538196 6538196 6538196 GGAGTAAGACCCCTGGACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTGC GGAGTAAGACCCCTGGACCACCAGCCCCAGCAGGAGCACAAGAGGAAGAGAGAGACCCTCACTGC A G GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr12:6537549..6538366;chr12:6538101..6538375 26863196,32194978 MeRIP-seq:(Medium) rs1393056924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426007,Human_RBP_ID_1476008,Human_RBP_ID_3411546,Human_RBP_ID_6209879,Human_RBP_ID_12009544,Human_RBP_ID_17240176,Human_RBP_ID_17355709,Human_RBP_ID_17650301,Human_RBP_ID_18188702,Human_RBP_ID_18631586,Human_RBP_ID_22435753,Human_RBP_ID_22532409,Human_RBP_ID_27424469 Human_Splice_Rec_1328616,Human_Splice_Rec_1328632,Human_Splice_Rec_1328662,Human_Splice_Rec_1328676,Human_Splice_Rec_1328688,Human_Splice_Rec_1328702,Human_Splice_Rec_1328708,Human_Splice_Rec_1328722,Human_Splice_Rec_1328734 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 91507 RMVar_ID_91507 Human_SNP_ID_489490212 m1A Human chr12 + 6538210 6538209 6538211 GGACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTGCTGGGGAGTCCCTGC GGACCACCAGCCCCAGCAAGAGCACAAGAGGA__AGAGAGACCCTCACTGCTGGGGAGTCCCTGC AAG A GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6538160..6538315 26863196 MeRIP-seq:(Medium) rs752810735 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_426009,Human_RBP_ID_17356890,Human_RBP_ID_17650564,Human_RBP_ID_22436213,Human_RBP_ID_27424470 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 91508 RMVar_ID_91508 Human_SNP_ID_489490214 m1A Human chr12 + 6538212 6538212 6538212 ACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTGCTGGGGAGTCCCTGCCA ACCACCAGCCCCAGCAAGAGCACAAGAGGAAGCGAGAGACCCTCACTGCTGGGGAGTCCCTGCCA A C GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6538165..6538338 26863196 MeRIP-seq:(Medium) rs781711772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426009,Human_RBP_ID_17356890,Human_RBP_ID_17650564,Human_RBP_ID_22436213,Human_RBP_ID_27424470 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 91509 RMVar_ID_91509 Human_SNP_ID_489490217 m1A Human chr12 + 6538216 6538216 6538216 CCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTGCTGGGGAGTCCCTGCCACACT CCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGCGACCCTCACTGCTGGGGAGTCCCTGCCACACT A C GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:6538166..6538375 26863196 MeRIP-seq:(Medium) rs756260656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17356890,Human_RBP_ID_27424470 Human_miRNA_ID_473654 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 91510 RMVar_ID_91510 Human_SNP_ID_489495866 m1A Human chr12 - 6556951 6556951 6556951 AACTAGACGGGTGGCTCACTGCCATTGTCACCAGGTTGGAACTCTTGCCTCTGTGAGGATGCCTT AACTAGACGGGTGGCTCACTGCCATTGTCACCGGGTTGGAACTCTTGCCTCTGTGAGGATGCCTT T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6556901..6557118 26863196 MeRIP-seq:(Medium) rs767495838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1799282,Human_RBP_ID_2349656,Human_RBP_ID_4237651,Human_RBP_ID_8381958,Human_RBP_ID_12010012,Human_RBP_ID_17650568,Human_RBP_ID_18631643,Human_RBP_ID_22795101,Human_RBP_ID_23207526,Human_RBP_ID_27217608,Human_RBP_ID_27558232 Human_miRNA_ID_1414216,Human_miRNA_ID_1414217,Human_miRNA_ID_2346057,Human_miRNA_ID_2723881 RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 91511 RMVar_ID_91511 Human_SNP_ID_489495925 m1A Human chr12 - 6557070 6557070 6557070 CCAAGGGGCCTCAGCCTCCCACTGTGTCTCCCATCCGTTCCAGCCGCCCCCCACCAGCAAAGAGG CCAAGGGGCCTCAGCCTCCCACTGTGTCTCCCGTCCGTTCCAGCCGCCCCCCACCAGCAAAGAGG T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6556958..6557365 26863196 MeRIP-seq:(Medium) rs1383275217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753391,Human_RBP_ID_6210125,Human_RBP_ID_27424485 Human_miRNA_ID_87980,Human_miRNA_ID_87981,Human_miRNA_ID_2386904,Human_miRNA_ID_2388380,Human_miRNA_ID_3030584 RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 91512 RMVar_ID_91512 Human_SNP_ID_489498029 m1A Human chr12 - 6563749 6563749 6563749 CTGTTTCTAGGATCCAGTGGAGTGAAGAGGAGACCGAGGACGAGGAGGAAGAGAAAGAAGTGACC CTGTTTCTAGGATCCAGTGGAGTGAAGAGGAGTCCGAGGACGAGGAGGAAGAGAAAGAAGTGACC T A NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6563476..6563950 26863196 MeRIP-seq:(Medium) rs773716188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36538,Human_RBP_ID_229844,Human_RBP_ID_874188,Human_RBP_ID_6210217,Human_RBP_ID_9364550,Human_RBP_ID_18976712,Human_RBP_ID_27805241 Human_Splice_Rec_1328938,Human_Splice_Rec_1328968,Human_Splice_Rec_1328998,Human_Splice_Rec_1329026,Human_Splice_Rec_1329056,Human_Splice_Rec_1329084,Human_Splice_Rec_1329112,Human_Splice_Rec_1329154,Human_Splice_Rec_1329194,Human_Splice_Rec_1329212,Human_Splice_Rec_1329214,Human_Splice_Rec_1329346,Human_Splice_Rec_1329370 RMVar_hsa_circ_63050,RMVar_hsa_circ_38844 91513 RMVar_ID_91513 Human_SNP_ID_489498873 m1A Human chr12 + 6566374 6566374 6566374 GGTTTGAAGAGTCCTGGACTAATGGCAGCCACACATTCCCTGGCCCCACACCCTGGGAGCCTGTA GGTTTGAAGAGTCCTGGACTAATGGCAGCCACGCATTCCCTGGCCCCACACCCTGGGAGCCTGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6566370..6566519 26863196 MeRIP-seq:(Medium) rs200372059 Functional Loss SNV dbSNP153 33..33 33 - - - 91514 RMVar_ID_91514 Human_SNP_ID_489498954 m1A Human chr12 + 6566601 6566601 6566601 CTTATTTGTCTTAGGGGCTTCAACAGAGCCCAATCTCCTCTTGGCTGCCCTGAAAAGACACAAGA CTTATTTGTCTTAGGGGCTTCAACAGAGCCCAGTCTCCTCTTGGCTGCCCTGAAAAGACACAAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6566551..6566625 26863196 MeRIP-seq:(Medium) rs542297827 Functional Loss SNV dbSNP153 33..33 33 - - - 91515 RMVar_ID_91515 Human_SNP_ID_489499441 m1A Human chr12 - 6568092 6568091 6568092 TTTCAGGTGGGAGGGCGTTCGGTCGGGCCTCCAGGGGGATAGCGGGGGTGCTTGAGTCGCGGGTG TTTCAGGTGGGAGGGCGTTCGGTCGGGCCTCC_GGGGGATAGCGGGGGTGCTTGAGTCGCGGGTG CT C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:6568086..6568300 26863196 MeRIP-seq:(Medium) rs984822671 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5348093,Human_RBP_ID_19060020,Human_RBP_ID_21966971,Human_RBP_ID_26777218 91516 RMVar_ID_91516 Human_SNP_ID_489499458 m1A Human chr12 - 6568141 6568141 6568141 GCAGCACTGACCTGGTCTGGGACGTGGGGAGAAGGGTGCGCTACCTGGGTTTCAGGTGGGAGGGC GCAGCACTGACCTGGTCTGGGACGTGGGGAGAGGGGTGCGCTACCTGGGTTTCAGGTGGGAGGGC T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:6568103..6568216 26863196 MeRIP-seq:(Medium) rs555322532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5348093,Human_RBP_ID_18976716,Human_RBP_ID_21966971 Human_Splice_Rec_1329045,Human_Splice_Rec_1329215,Human_Splice_Rec_1329225,Human_Splice_Rec_1329233,Human_Splice_Rec_1329247 RMVar_hsa_circ_19023 91517 RMVar_ID_91517 Human_SNP_ID_489501013 m1A Human chr12 + 6573052 6573052 6573052 TGCAGTCAGATCAGGGAGGCCGAATCGGCAGGAGGCAGGGGAGCCACTGGCTACCTTTGTGCAGG TGCAGTCAGATCAGGGAGGCCGAATCGGCAGGGGGCAGGGGAGCCACTGGCTACCTTTGTGCAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6573051..6573200 32194978 MeRIP-seq:(Medium) rs763677195 Functional Loss SNV dbSNP153 33..33 33 - - - 91518 RMVar_ID_91518 Human_SNP_ID_489501014 m1A Human chr12 + 6573052 6573052 6573052 TGCAGTCAGATCAGGGAGGCCGAATCGGCAGGAGGCAGGGGAGCCACTGGCTACCTTTGTGCAGG TGCAGTCAGATCAGGGAGGCCGAATCGGCAGGTGGCAGGGGAGCCACTGGCTACCTTTGTGCAGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6573051..6573200 32194978 MeRIP-seq:(Medium) rs763677195 Functional Loss SNV dbSNP153 33..33 33 - - - 91519 RMVar_ID_91519 Human_SNP_ID_489502660 m1A Human chr12 + 6578913 6578913 6578913 GCTGACTTTTCCTCCACCTTCTCTACATCAGCAGCACCTAGGGGAAGAAATGTTATTGAGACTAT GCTGACTTTTCCTCCACCTTCTCTACATCAGCGGCACCTAGGGGAAGAAATGTTATTGAGACTAT A G AC006064.2 Ensembl:ENSG00000247853 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6578826..6578925 32194978 MeRIP-seq:(Medium) rs144216235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8071717 91520 RMVar_ID_91520 Human_SNP_ID_489503510 m1A Human chr12 - 6581067 6581067 6581067 GGAAAAGGCAGAGGTGAAGGAGAGAACAGAGGAACCTATGGAGACAGAGCCCAAAGGTAAAGGTA GGAAAAGGCAGAGGTGAAGGAGAGAACAGAGGTACCTATGGAGACAGAGCCCAAAGGTAAAGGTA T A CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6578451..6581202 26863196 MeRIP-seq:(Medium) rs1303582400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3597,Human_RBP_ID_4237901,Human_RBP_ID_5561008,Human_RBP_ID_6210441,Human_RBP_ID_8784516,Human_RBP_ID_12010493,Human_RBP_ID_18544195,Human_RBP_ID_22907402,Human_RBP_ID_26321126,Human_RBP_ID_26768351,Human_RBP_ID_27571938,Human_RBP_ID_27805246 Human_Splice_Rec_1329323,Human_Splice_Rec_1329451,Human_Splice_Rec_1329525,Human_Splice_Rec_1329603,Human_Splice_Rec_1329681,Human_Splice_Rec_1329771,Human_Splice_Rec_1329801,Human_Splice_Rec_1329877,Human_Splice_Rec_1329957,Human_Splice_Rec_1329985,Human_Splice_Rec_1330063,Human_Splice_Rec_1330079,Human_Splice_Rec_1330107,Human_Splice_Rec_1330181,Human_Splice_Rec_1330259,Human_Splice_Rec_1330337,Human_Splice_Rec_1330365,Human_Splice_Rec_1330437,Human_Splice_Rec_1330509,Human_Splice_Rec_1330585,Human_Splice_Rec_1330635,Human_Splice_Rec_1330711,Human_Splice_Rec_1330777,Human_Splice_Rec_1330803,Human_Splice_Rec_1330835,Human_Splice_Rec_1330913,Human_Splice_Rec_1331037,Human_Splice_Rec_1331099,Human_Splice_Rec_1331159 Human_miRNA_ID_3069285 RMVar_hsa_circ_100510,RMVar_hsa_circ_102778,RMVar_hsa_circ_154580,RMVar_hsa_circ_154581,RMVar_hsa_circ_354597,RMVar_hsa_circ_26119,RMVar_hsa_circ_154584,RMVar_hsa_circ_154585,RMVar_hsa_circ_93404,RMVar_hsa_circ_267036,RMVar_hsa_circ_154586,RMVar_hsa_circ_308781,RMVar_hsa_circ_154587 91521 RMVar_ID_91521 Human_SNP_ID_489503535 m1A Human chr12 + 6581126 6581124 6581127 TTTTCCACTTTCTCCTCTCCCTCAGGGGGTTCAACAACGACCTTTTCATCCTCTGAGGCAGGGGC TTTTCCACTTTCTCCTCTCCCTCAGGGGGTT___CAACGACCTTTTCATCCTCTGAGGCAGGGGC TCAA T AC006064.2 Ensembl:ENSG00000247853 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6581026..6581175 32194978 MeRIP-seq:(Medium) rs1213915459 Functional Loss DEL dbSNP153 32..34 33 - - - 91522 RMVar_ID_91522 Human_SNP_ID_489503536 m1A Human chr12 + 6581126 6581126 6581126 TTTTCCACTTTCTCCTCTCCCTCAGGGGGTTCAACAACGACCTTTTCATCCTCTGAGGCAGGGGC TTTTCCACTTTCTCCTCTCCCTCAGGGGGTTCCACAACGACCTTTTCATCCTCTGAGGCAGGGGC A C AC006064.2 Ensembl:ENSG00000247853 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6581026..6581175 32194978 MeRIP-seq:(Medium) rs1423643965 Functional Loss SNV dbSNP153 33..33 33 - - - 91523 RMVar_ID_91523 Human_SNP_ID_489503582 m1A Human chr12 + 6581199 6581199 6581199 GTGTACACTTCAAAGGAAAAAAAAACAAAAACAAAACAGATGAAGCAGACAGGCCAGCAACTAAA GTGTACACTTCAAAGGAAAAAAAAACAAAAACCAAACAGATGAAGCAGACAGGCCAGCAACTAAA A C AC006064.2 Ensembl:ENSG00000247853 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6581197..6581325 26863196 MeRIP-seq:(Medium) rs778917476 Functional Loss SNV dbSNP153 33..33 33 - - - 91524 RMVar_ID_91524 Human_SNP_ID_489509262 m1A Human chr12 - 6599948 6599948 6599948 GGACAATTCGGAGGGTGAGGAGATCCTGGAAGAGGTTGGGGGAGACCTCGAAGAGGAGGATGACC GGACAATTCGGAGGGTGAGGAGATCCTGGAAGTGGTTGGGGGAGACCTCGAAGAGGAGGATGACC T A CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6599901..6600025 26863196 MeRIP-seq:(Medium) rs770181976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228782,Human_RBP_ID_753401,Human_RBP_ID_872899,Human_RBP_ID_1799430,Human_RBP_ID_5521338,Human_RBP_ID_6210577,Human_RBP_ID_8382050,Human_RBP_ID_8784627,Human_RBP_ID_9278897,Human_RBP_ID_9364587,Human_RBP_ID_17830686,Human_RBP_ID_18469115,Human_RBP_ID_18975300,Human_RBP_ID_22436835,Human_RBP_ID_24551197,Human_RBP_ID_26321153,Human_RBP_ID_27571946,Human_RBP_ID_27806423 Human_Splice_Rec_1329276,Human_Splice_Rec_1329404,Human_Splice_Rec_1329480,Human_Splice_Rec_1329556,Human_Splice_Rec_1329634,Human_Splice_Rec_1329724,Human_Splice_Rec_1329910,Human_Splice_Rec_1330016,Human_Splice_Rec_1330136,Human_Splice_Rec_1330212,Human_Splice_Rec_1330290,Human_Splice_Rec_1330390,Human_Splice_Rec_1330464,Human_Splice_Rec_1330540,Human_Splice_Rec_1330730,Human_Splice_Rec_1330866,Human_Splice_Rec_1330990,Human_Splice_Rec_1331054,Human_Splice_Rec_1331112 RMVar_hsa_circ_267036,RMVar_hsa_circ_92656,RMVar_hsa_circ_154589,RMVar_hsa_circ_46896,RMVar_hsa_circ_154593,RMVar_hsa_circ_371110,RMVar_hsa_circ_85287,RMVar_hsa_circ_375998,RMVar_hsa_circ_98669,RMVar_hsa_circ_81148,RMVar_hsa_circ_107940,RMVar_hsa_circ_154594,RMVar_hsa_circ_154596,RMVar_hsa_circ_154597,RMVar_hsa_circ_154595,RMVar_hsa_circ_268431,RMVar_hsa_circ_40049,RMVar_hsa_circ_100472,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600 91525 RMVar_ID_91525 Human_SNP_ID_489509681 m1A Human chr12 - 6601024 6601024 6601024 TAGGTCCCAATGCTCGGAGGAAGCCCAAGGGCAGCCCTCGTGTACCTGATGCCAAGAAGCCTAAA TAGGTCCCAATGCTCGGAGGAAGCCCAAGGGCGGCCCTCGTGTACCTGATGCCAAGAAGCCTAAA T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6600951..6601508 32194978 MeRIP-seq:(Medium) rs375091307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426157,Human_RBP_ID_8786605,Human_RBP_ID_9279525 Human_Splice_Rec_1329270,Human_Splice_Rec_1329271,Human_Splice_Rec_1329398,Human_Splice_Rec_1329399,Human_Splice_Rec_1329474,Human_Splice_Rec_1329475,Human_Splice_Rec_1329550,Human_Splice_Rec_1329551,Human_Splice_Rec_1329628,Human_Splice_Rec_1329629,Human_Splice_Rec_1329718,Human_Splice_Rec_1329719,Human_Splice_Rec_1329904,Human_Splice_Rec_1329905,Human_Splice_Rec_1330010,Human_Splice_Rec_1330011,Human_Splice_Rec_1330130,Human_Splice_Rec_1330131,Human_Splice_Rec_1330206,Human_Splice_Rec_1330207,Human_Splice_Rec_1330284,Human_Splice_Rec_1330285,Human_Splice_Rec_1330384,Human_Splice_Rec_1330385,Human_Splice_Rec_1330458,Human_Splice_Rec_1330459,Human_Splice_Rec_1330534,Human_Splice_Rec_1330535,Human_Splice_Rec_1330860,Human_Splice_Rec_1330861,Human_Splice_Rec_1330984,Human_Splice_Rec_1330985,Human_Splice_Rec_1331048,Human_Splice_Rec_1331049,Human_Splice_Rec_1331106,Human_Splice_Rec_1331107,Human_Splice_Rec_1331238,Human_Splice_Rec_1331239 RMVar_hsa_circ_267036,RMVar_hsa_circ_46896,RMVar_hsa_circ_85287,RMVar_hsa_circ_375998,RMVar_hsa_circ_81148,RMVar_hsa_circ_107940,RMVar_hsa_circ_154594,RMVar_hsa_circ_154596,RMVar_hsa_circ_154595,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602,RMVar_hsa_circ_80292,RMVar_hsa_circ_154601 91526 RMVar_ID_91526 Human_SNP_ID_489510090 m1A Human chr12 - 6602105 6602105 6602105 GGAGGGGCCAGAGTTTGTGGAGGAGGAGGAAGAGGTGGCTCTGCGCTCAGACAGTGAGGGCAGCG GGAGGGGCCAGAGTTTGTGGAGGAGGAGGAAGGGGTGGCTCTGCGCTCAGACAGTGAGGGCAGCG T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6601951..6602200 26863196 MeRIP-seq:(Medium) rs770418109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_195252,Human_RBP_ID_228784,Human_RBP_ID_753405,Human_RBP_ID_810892,Human_RBP_ID_877150,Human_RBP_ID_1479512,Human_RBP_ID_6210619,Human_RBP_ID_9278903,Human_RBP_ID_22039144,Human_RBP_ID_24543044,Human_RBP_ID_26322646,Human_RBP_ID_27805257 Human_Splice_Rec_1329264,Human_Splice_Rec_1329392,Human_Splice_Rec_1329468,Human_Splice_Rec_1329544,Human_Splice_Rec_1329622,Human_Splice_Rec_1329712,Human_Splice_Rec_1329898,Human_Splice_Rec_1330004,Human_Splice_Rec_1330124,Human_Splice_Rec_1330200,Human_Splice_Rec_1330278,Human_Splice_Rec_1330378,Human_Splice_Rec_1330452,Human_Splice_Rec_1330528,Human_Splice_Rec_1330854,Human_Splice_Rec_1330978,Human_Splice_Rec_1331042,Human_Splice_Rec_1331232,Human_Splice_Rec_1331244,Human_Splice_Rec_1331250 RMVar_hsa_circ_267036,RMVar_hsa_circ_46896,RMVar_hsa_circ_85287,RMVar_hsa_circ_81148,RMVar_hsa_circ_107940,RMVar_hsa_circ_154594,RMVar_hsa_circ_154595,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 91527 RMVar_ID_91527 Human_SNP_ID_489510189 m1A Human chr12 - 6602354 6602354 6602354 AAAAAAAGGAGGTGAGTGGGTGACTGAATGTTACGGGGAATCAGAGGAAGAAGGGAGGAGCTCTG AAAAAAAGGAGGTGAGTGGGTGACTGAATGTTTCGGGGAATCAGAGGAAGAAGGGAGGAGCTCTG T A CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6602351..6602529 26863196 MeRIP-seq:(Medium) rs529188545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5349198,Human_RBP_ID_19055839,Human_RBP_ID_22574076,Human_RBP_ID_23570859 RMVar_hsa_circ_46896,RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 91528 RMVar_ID_91528 Human_SNP_ID_489510208 m1A Human chr12 - 6602392 6602392 6602392 GAAACCTCGGGACCCTAAAATCCCTAAGAGCAAGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA GAAACCTCGGGACCCTAAAATCCCTAAGAGCAGGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6602376..6602539 26863196 MeRIP-seq:(Medium) rs774371323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364600,Human_RBP_ID_18434662,Human_RBP_ID_24543045,Human_RBP_ID_26321162,Human_RBP_ID_26910589 Human_Splice_Rec_1329263,Human_Splice_Rec_1329391,Human_Splice_Rec_1329466,Human_Splice_Rec_1329467,Human_Splice_Rec_1329543,Human_Splice_Rec_1329621,Human_Splice_Rec_1329711,Human_Splice_Rec_1329897,Human_Splice_Rec_1330003,Human_Splice_Rec_1330123,Human_Splice_Rec_1330199,Human_Splice_Rec_1330277,Human_Splice_Rec_1330377,Human_Splice_Rec_1330451,Human_Splice_Rec_1330527,Human_Splice_Rec_1330853,Human_Splice_Rec_1330977,Human_Splice_Rec_1331041,Human_Splice_Rec_1331231,Human_Splice_Rec_1331243,Human_Splice_Rec_1331249 RMVar_hsa_circ_24388,RMVar_hsa_circ_46896,RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 91529 RMVar_ID_91529 Human_SNP_ID_489510228 m1A Human chr12 - 6602438 6602438 6602438 TGTCAGAAACAGAGACTCCAAAGCTCAAGAAGAAGAAAAAGCCTAAGAAACCTCGGGACCCTAAA TGTCAGAAACAGAGACTCCAAAGCTCAAGAAGGAGAAAAAGCCTAAGAAACCTCGGGACCCTAAA T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:6602336..6602540 26863196 MeRIP-seq:(Medium) rs1171745254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34266,Human_RBP_ID_877151,Human_RBP_ID_1799446,Human_RBP_ID_3411770,Human_RBP_ID_9364600,Human_RBP_ID_18410844,Human_RBP_ID_22907495,Human_RBP_ID_24543045,Human_RBP_ID_26321162,Human_RBP_ID_27805258 Human_Splice_Rec_1329262,Human_Splice_Rec_1329263,Human_Splice_Rec_1329390,Human_Splice_Rec_1329391,Human_Splice_Rec_1329466,Human_Splice_Rec_1329467,Human_Splice_Rec_1329542,Human_Splice_Rec_1329543,Human_Splice_Rec_1329620,Human_Splice_Rec_1329621,Human_Splice_Rec_1329710,Human_Splice_Rec_1329711,Human_Splice_Rec_1329896,Human_Splice_Rec_1329897,Human_Splice_Rec_1330002,Human_Splice_Rec_1330003,Human_Splice_Rec_1330122,Human_Splice_Rec_1330123,Human_Splice_Rec_1330198,Human_Splice_Rec_1330199,Human_Splice_Rec_1330276,Human_Splice_Rec_1330277,Human_Splice_Rec_1330376,Human_Splice_Rec_1330377,Human_Splice_Rec_1330450,Human_Splice_Rec_1330451,Human_Splice_Rec_1330526,Human_Splice_Rec_1330527,Human_Splice_Rec_1330852,Human_Splice_Rec_1330853,Human_Splice_Rec_1330976,Human_Splice_Rec_1330977,Human_Splice_Rec_1331040,Human_Splice_Rec_1331041,Human_Splice_Rec_1331230,Human_Splice_Rec_1331231,Human_Splice_Rec_1331242,Human_Splice_Rec_1331243,Human_Splice_Rec_1331248,Human_Splice_Rec_1331249,Human_Splice_Rec_1331252 RMVar_hsa_circ_24388,RMVar_hsa_circ_46896,RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 91530 RMVar_ID_91530 Human_SNP_ID_489510252 m1A Human chr12 + 6602493 6602493 6602493 GTTTCTGACAAATCCTCTTCTGGGTCCTCTTCATTTTCTACATATATTTGGCAAAGAGTGGTAGG GTTTCTGACAAATCCTCTTCTGGGTCCTCTTCGTTTTCTACATATATTTGGCAAAGAGTGGTAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr12:6602476..6602500;chr12:6602376..6602500;chr12:6601724..6602947 26863196,32194978 MeRIP-seq:(Medium) rs1565619678 Functional Loss SNV dbSNP153 33..33 33 - - - 91531 RMVar_ID_91531 Human_SNP_ID_489511509 m1A Human chr12 - 6606331 6606331 6606331 GCCTGGGCTCCCCGTCCCCCTGCTCGGCGGGCAGTGAGGAGGAGGATATGGATGCACTTTTGAAC GCCTGGGCTCCCCGTCCCCCTGCTCGGCGGGCGGTGAGGAGGAGGATATGGATGCACTTTTGAAC T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:6606251..6606533;chr12:6606251..6606493;chr12:6606233..6606506 26863196 MeRIP-seq:(Medium) rs763513049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34269,Human_RBP_ID_228785,Human_RBP_ID_4245965,Human_RBP_ID_6210734,Human_RBP_ID_8787171,Human_RBP_ID_9278905,Human_RBP_ID_9322984,Human_RBP_ID_18631836,Human_RBP_ID_27217718 Human_Splice_Rec_1329261,Human_Splice_Rec_1329389,Human_Splice_Rec_1329465,Human_Splice_Rec_1329541,Human_Splice_Rec_1329619,Human_Splice_Rec_1329709,Human_Splice_Rec_1329895,Human_Splice_Rec_1330001,Human_Splice_Rec_1330121,Human_Splice_Rec_1330197,Human_Splice_Rec_1330275,Human_Splice_Rec_1330375,Human_Splice_Rec_1330449,Human_Splice_Rec_1330525,Human_Splice_Rec_1330851,Human_Splice_Rec_1330975,Human_Splice_Rec_1331039,Human_Splice_Rec_1331229,Human_Splice_Rec_1331247,Human_Splice_Rec_1331251 RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600 91532 RMVar_ID_91532 Human_SNP_ID_489511530 m1A Human chr12 + 6606360 6606360 6606360 CACTGCCCGCCGAGCAGGGGGACGGGGAGCCCAGGCCCGACGCCATCCCCTTCCGCTCCCGGCCA CACTGCCCGCCGAGCAGGGGGACGGGGAGCCCCGGCCCGACGCCATCCCCTTCCGCTCCCGGCCA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:6606251..6606545;chr12:6606251..6606529 26863196 MeRIP-seq:(Medium) rs1220173964 Functional Loss SNV dbSNP153 33..33 33 - - - 91533 RMVar_ID_91533 Human_SNP_ID_489512517 m1A Human chr12 + 6608054 6608054 6608054 ATCCCATAATAGTCAGAAACTCACCCCCCCCCATACTACAACAACGGACACTCGGCCTCCTCCCA ATCCCATAATAGTCAGAAACTCACCCCCCCCCGTACTACAACAACGGACACTCGGCCTCCTCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6608049..6608308 26863196 MeRIP-seq:(Medium) rs1485676295 Functional Loss SNV dbSNP153 33..33 33 - - - 91534 RMVar_ID_91534 Human_SNP_ID_489512531 m1A Human chr12 + 6608090 6608090 6608090 TACAACAACGGACACTCGGCCTCCTCCCACACACATCCCGTAATAATCAGTCTCCCACTTTCTAT TACAACAACGGACACTCGGCCTCCTCCCACACCCATCCCGTAATAATCAGTCTCCCACTTTCTAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6608086..6608292 26863196 MeRIP-seq:(Medium) rs972991984 Functional Loss SNV dbSNP153 33..33 33 - - - 91535 RMVar_ID_91535 Human_SNP_ID_489512545 m1A Human chr12 + 6608136 6608133 6608136 TCAGTCTCCCACTTTCTATACTGACATCCCATAATAACTAACCCCCTAGAGCTGCCCTCAGTCCC TCAGTCTCCCACTTTCTATACTGACATCCC___ATAACTAACCCCCTAGAGCTGCCCTCAGTCCC CATA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6608128..6608365 26863196 MeRIP-seq:(Medium) rs1320653714 Functional Loss DEL dbSNP153 31..33 33 - - - 91536 RMVar_ID_91536 Human_SNP_ID_489527904 m1A Human chr12 - 6662942 6662942 6662942 AGAAGGTCACAATTATGAAGCGGTTCTGTGGCAGGAAATATTGGAGGGTGCGGAGAAAGAGGGGG AGAAGGTCACAATTATGAAGCGGTTCTGTGGCGGGAAATATTGGAGGGTGCGGAGAAAGAGGGGG T C ING4 Ensembl:ENSG00000111653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6662940..6663080 26863196 MeRIP-seq:(Medium) rs1195323797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12013109 91537 RMVar_ID_91537 Human_SNP_ID_489527907 m1A Human chr12 + 6662962 6662962 6662962 TCCAATATTTCCTGCCACAGAACCGCTTCATAATTGTGACCTTCTCGTCACTGGAACTTAAGGGC TCCAATATTTCCTGCCACAGAACCGCTTCATAGTTGTGACCTTCTCGTCACTGGAACTTAAGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6662960..6663081 26863196 MeRIP-seq:(Medium) rs1213788243 Functional Loss SNV dbSNP153 33..33 33 - - - 91538 RMVar_ID_91538 Human_SNP_ID_489532222 m1A Human chr12 - 6678285 6678285 6678285 AAGAAGGTAGCATCGACCCTAACCGAGGAAGGAGGCGGAGGTGGTGGTGGAGGTGGCAGTGTGGC AAGAAGGTAGCATCGACCCTAACCGAGGAAGGTGGCGGAGGTGGTGGTGGAGGTGGCAGTGTGGC T A ZNF384 Ensembl:ENSG00000126746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6678235..6678427 26863196 MeRIP-seq:(Medium) rs764884473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753572,Human_RBP_ID_810716,Human_RBP_ID_9366106,Human_RBP_ID_18976725 Human_Splice_Rec_1331614 RMVar_hsa_circ_118666,RMVar_hsa_circ_331498,RMVar_hsa_circ_100240,RMVar_hsa_circ_154606,RMVar_hsa_circ_154608,RMVar_hsa_circ_154610,RMVar_hsa_circ_85152,RMVar_hsa_circ_154609,RMVar_hsa_circ_295570,RMVar_hsa_circ_26086,RMVar_hsa_circ_154611,RMVar_hsa_circ_154613,RMVar_hsa_circ_315312,RMVar_hsa_circ_369638,RMVar_hsa_circ_86321,RMVar_hsa_circ_154612 91539 RMVar_ID_91539 Human_SNP_ID_489532223 m1A Human chr12 - 6678285 6678285 6678285 AAGAAGGTAGCATCGACCCTAACCGAGGAAGGAGGCGGAGGTGGTGGTGGAGGTGGCAGTGTGGC AAGAAGGTAGCATCGACCCTAACCGAGGAAGGCGGCGGAGGTGGTGGTGGAGGTGGCAGTGTGGC T G ZNF384 Ensembl:ENSG00000126746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6678235..6678427 26863196 MeRIP-seq:(Medium) rs764884473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753572,Human_RBP_ID_810716,Human_RBP_ID_9366106,Human_RBP_ID_18976725 Human_Splice_Rec_1331614 RMVar_hsa_circ_118666,RMVar_hsa_circ_331498,RMVar_hsa_circ_100240,RMVar_hsa_circ_154606,RMVar_hsa_circ_154608,RMVar_hsa_circ_154610,RMVar_hsa_circ_85152,RMVar_hsa_circ_154609,RMVar_hsa_circ_295570,RMVar_hsa_circ_26086,RMVar_hsa_circ_154611,RMVar_hsa_circ_154613,RMVar_hsa_circ_315312,RMVar_hsa_circ_369638,RMVar_hsa_circ_86321,RMVar_hsa_circ_154612 91540 RMVar_ID_91540 Human_SNP_ID_489535022 m1A Human chr12 + 6688509 6688507 6688509 CTCAGAGACTGGTCCTTGTTCGTTCCCAGGCCACAGGTAACCAGGGGTCAGAGAACATTAGAGAT CTCAGAGACTGGTCCTTGTTCGTTCCCAGGC__CAGGTAACCAGGGGTCAGAGAACATTAGAGAT CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6688507..6688601 26863196 MeRIP-seq:(Medium) rs1450543737 Functional Loss DEL dbSNP153 32..33 33 - - - 91541 RMVar_ID_91541 Human_SNP_ID_489535127 m1A Human chr12 + 6688886 6688886 6688886 TTCCTTGGGACGTCCCTCCTTCCCCTCCAGGGAGCTGAACTCTGCCACCCACCAGACAGGCACCC TTCCTTGGGACGTCCCTCCTTCCCCTCCAGGGTGCTGAACTCTGCCACCCACCAGACAGGCACCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:6688693..6688939;chr12:6688391..6688960 26863196 MeRIP-seq:(Medium) rs1433998033 Functional Loss SNV dbSNP153 33..33 33 - - - 91542 RMVar_ID_91542 Human_SNP_ID_489535131 m1A Human chr12 - 6688894 6688894 6688894 TAGGGGGCGGGTGCCTGTCTGGTGGGTGGCAGAGTTCAGCTCCCTGGAGGGGAAGGAGGGACGTC TAGGGGGCGGGTGCCTGTCTGGTGGGTGGCAGTGTTCAGCTCCCTGGAGGGGAAGGAGGGACGTC T A ZNF384 Ensembl:ENSG00000126746 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:6688691..6688981 26863196 MeRIP-seq:(Medium) rs1448131049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755611,Human_RBP_ID_3418237,Human_RBP_ID_5171745,Human_RBP_ID_9415815,Human_RBP_ID_18417223,Human_RBP_ID_18934238,Human_RBP_ID_22040512,Human_RBP_ID_23571488 Human_Splice_Rec_1331667 91543 RMVar_ID_91543 Human_SNP_ID_489538263 m1A Human chr12 - 6700643 6700643 6700643 CCCCCCAGCCCCGCTCAGTCCCGAGCGCCCGCAGTCGTCGCGCCGCCGCGCCAAGCATGCAGGTG CCCCCCAGCCCCGCTCAGTCCCGAGCGCCCGCGGTCGTCGCGCCGCCGCGCCAAGCATGCAGGTG T C PIANP Ensembl:ENSG00000139200 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:6700550..6700784 26863196 MeRIP-seq:(Medium) rs1265596630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1331711,Human_Splice_Rec_1331721 91544 RMVar_ID_91544 Human_SNP_ID_489538291 m1A Human chr12 - 6700743 6700743 6700743 CCGCCGCCCCGCGCCCCAGGCGCCCGCCCCCCACCCGCTCCAGCGCCCTGCCGCGGGCCAAACCT CCGCCGCCCCGCGCCCCAGGCGCCCGCCCCCCCCCCGCTCCAGCGCCCTGCCGCGGGCCAAACCT T G PIANP Ensembl:ENSG00000139200 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:6700644..6700798 26863410 MeRIP-seq:(Medium) rs1013029438 Functional Loss SNV dbSNP153 33..33 33 - - - 91545 RMVar_ID_91545 Human_SNP_ID_489546658 m1A Human chr12 + 6724724 6724724 6724724 GGAGCAATTTCTGCTCCTAGCCAAGTCGGCCAAGGGGGCAGCGCTGGCCACACTCATCCATCAGG GGAGCAATTTCTGCTCCTAGCCAAGTCGGCCAGGGGGGCAGCGCTGGCCACACTCATCCATCAGG A G COPS7A Ensembl:ENSG00000111652 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6724676..6724750 32194978 MeRIP-seq:(Medium) rs1419984174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246489 Human_Splice_Rec_1331741,Human_Splice_Rec_1331753,Human_Splice_Rec_1331773,Human_Splice_Rec_1331787,Human_Splice_Rec_1331801,Human_Splice_Rec_1331815,Human_Splice_Rec_1331821,Human_Splice_Rec_1331833,Human_Splice_Rec_1331839,Human_Splice_Rec_1331845,Human_Splice_Rec_1331857,Human_Splice_Rec_1331869,Human_Splice_Rec_1331875,Human_Splice_Rec_1331887,Human_Splice_Rec_1331895,Human_Splice_Rec_1331903,Human_Splice_Rec_1331913,Human_Splice_Rec_1331927,Human_Splice_Rec_1331937,Human_Splice_Rec_1331945 Human_miRNA_ID_2151574,Human_miRNA_ID_2218025,Human_miRNA_ID_2420046 RMVar_hsa_circ_12814,RMVar_hsa_circ_88441,RMVar_hsa_circ_36664,RMVar_hsa_circ_154615,RMVar_hsa_circ_289996 91546 RMVar_ID_91546 Human_SNP_ID_489548040 m1A Human chr12 - 6729353 6729353 6729353 AGTCAACCTCGAGCCGCTGGTTGCGCTGGTCCAGGGAGCCACGAAGCACGTCAGCATACACAGCC AGTCAACCTCGAGCCGCTGGTTGCGCTGGTCCCGGGAGCCACGAAGCACGTCAGCATACACAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6729302..6729450 26863196 MeRIP-seq:(Medium) rs1251821808 Functional Loss SNV dbSNP153 33..33 33 - - - 91547 RMVar_ID_91547 Human_SNP_ID_489548644 m1A Human chr12 - 6731227 6731227 6731227 ACACATGAAGTCACAAAAAACAGAAAGTACCAACAAAAACATGACCTACATTTGCCTCCTCCCTA ACACATGAAGTCACAAAAAACAGAAAGTACCATCAAAAACATGACCTACATTTGCCTCCTCCCTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6731176..6731275 26863196 MeRIP-seq:(Medium) rs141139415 Functional Loss SNV dbSNP153 33..33 33 - - - 91548 RMVar_ID_91548 Human_SNP_ID_489553526 m1A Human chr12 - 6748535 6748533 6748535 CTCTCTCTTTCCCCCTCCAGGTACAGGCTGAGAGGCTGAGAAATCATCCCCTGAATAACTTTTTC CTCTCTCTTTCCCCCTCCAGGTACAGGCTGAG__GCTGAGAAATCATCCCCTGAATAACTTTTTC CCT C MLF2 Ensembl:ENSG00000089693 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6748144..6748816 32194978 MeRIP-seq:(Medium) rs1328607156 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_426473,Human_RBP_ID_873493,Human_RBP_ID_994134,Human_RBP_ID_6212733,Human_RBP_ID_9020302,Human_RBP_ID_12013792,Human_RBP_ID_17240308,Human_RBP_ID_17473292,Human_RBP_ID_17825475,Human_RBP_ID_18263434,Human_RBP_ID_19803083,Human_RBP_ID_21884445,Human_RBP_ID_22538497,Human_RBP_ID_22574083,Human_RBP_ID_22644579,Human_RBP_ID_22736631,Human_RBP_ID_23582825,Human_RBP_ID_24996339 Human_Splice_Rec_1331968,Human_Splice_Rec_1331984 Human_miRNA_ID_1500330 RMVar_hsa_circ_102617,RMVar_hsa_circ_126500,RMVar_hsa_circ_154618,RMVar_hsa_circ_154620,RMVar_hsa_circ_98180,RMVar_hsa_circ_154619 91549 RMVar_ID_91549 Human_SNP_ID_489553656 m1A Human chr12 - 6748913 6748913 6748913 GACCTCCCGATTCCGGCAGCAGCGTCCCCTGGAGTTTCGGCGGCTTGAGTCCTCAGGGGCTGGGG GACCTCCCGATTCCGGCAGCAGCGTCCCCTGGTGTTTCGGCGGCTTGAGTCCTCAGGGGCTGGGG T A MLF2 Ensembl:ENSG00000089693 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1398904823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426482,Human_RBP_ID_6212734,Human_RBP_ID_8382322,Human_RBP_ID_9020303,Human_RBP_ID_18976734,Human_RBP_ID_22436216,Human_RBP_ID_23113431 Human_Splice_Rec_1331966,Human_Splice_Rec_1331982,Human_Splice_Rec_1331988,Human_Splice_Rec_1332002,Human_Splice_Rec_1332016,Human_Splice_Rec_1332030 Human_miRNA_ID_119273,Human_miRNA_ID_123080,Human_miRNA_ID_1266982,Human_miRNA_ID_3010669 RMVar_hsa_circ_102617,RMVar_hsa_circ_126500,RMVar_hsa_circ_154618,RMVar_hsa_circ_154620,RMVar_hsa_circ_98180,RMVar_hsa_circ_154619 91550 RMVar_ID_91550 Human_SNP_ID_489553669 m1A Human chr12 - 6748928 6748928 6748928 CGAGTGGCGGCGGGAGACCTCCCGATTCCGGCAGCAGCGTCCCCTGGAGTTTCGGCGGCTTGAGT CGAGTGGCGGCGGGAGACCTCCCGATTCCGGCTGCAGCGTCCCCTGGAGTTTCGGCGGCTTGAGT T A MLF2 Ensembl:ENSG00000089693 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6748731..6748931 26863196 MeRIP-seq:(Medium) rs1197041099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228562,Human_RBP_ID_426483,Human_RBP_ID_18975309,Human_RBP_ID_22436216,Human_RBP_ID_23113431,Human_RBP_ID_27558242 Human_Splice_Rec_1331966,Human_Splice_Rec_1331982,Human_Splice_Rec_1331988,Human_Splice_Rec_1332002,Human_Splice_Rec_1332016,Human_Splice_Rec_1332030 RMVar_hsa_circ_102617,RMVar_hsa_circ_126500,RMVar_hsa_circ_154618,RMVar_hsa_circ_154620,RMVar_hsa_circ_98180,RMVar_hsa_circ_154619 91551 RMVar_ID_91551 Human_SNP_ID_489554486 m1A Human chr12 - 6751652 6751652 6751652 TCCTGTAGGCTGGAGCTGTCTCCCCCTTTGGGATGCTGGGAATGGTGAGTCTTTATCTCCCTGTG TCCTGTAGGCTGGAGCTGTCTCCCCCTTTGGGGTGCTGGGAATGGTGAGTCTTTATCTCCCTGTG T C MLF2 Ensembl:ENSG00000089693 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6751651..6751700 32194978 MeRIP-seq:(Medium) rs1218123817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872117,Human_RBP_ID_1065308,Human_RBP_ID_4247237,Human_RBP_ID_5346430,Human_RBP_ID_8784891,Human_RBP_ID_9352796,Human_RBP_ID_9364609,Human_RBP_ID_19055854,Human_RBP_ID_27632415 Human_Splice_Rec_1331958,Human_Splice_Rec_1331959,Human_Splice_Rec_1331974,Human_Splice_Rec_1331975,Human_Splice_Rec_1331994,Human_Splice_Rec_1331995,Human_Splice_Rec_1332008,Human_Splice_Rec_1332009,Human_Splice_Rec_1332022,Human_Splice_Rec_1332023,Human_Splice_Rec_1332036,Human_Splice_Rec_1332037,Human_Splice_Rec_1332046,Human_Splice_Rec_1332047,Human_Splice_Rec_1332056,Human_Splice_Rec_1332057 Human_miRNA_ID_2421738,Human_miRNA_ID_2441571 RMVar_hsa_circ_126500,RMVar_hsa_circ_154620,RMVar_hsa_circ_154622,RMVar_hsa_circ_115443,RMVar_hsa_circ_101322,RMVar_hsa_circ_93795,RMVar_hsa_circ_154623,RMVar_hsa_circ_154625,RMVar_hsa_circ_90024,RMVar_hsa_circ_154624 91552 RMVar_ID_91552 Human_SNP_ID_489554612 m1A Human chr12 - 6752028 6752028 6752028 CCACAGGGATCCCTTTGCTATTCACCGTCAGCATATGAGCCGTATGTTGTCAGGTGGCTTTGGAT CCACAGGGATCCCTTTGCTATTCACCGTCAGCGTATGAGCCGTATGTTGTCAGGTGGCTTTGGAT T C MLF2 Ensembl:ENSG00000089693 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6751978..6752095 26863196 MeRIP-seq:(Medium) rs1016382445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275572,Human_RBP_ID_426491,Human_RBP_ID_994147,Human_RBP_ID_1168081,Human_RBP_ID_1476336,Human_RBP_ID_3941430,Human_RBP_ID_4246490,Human_RBP_ID_5111882,Human_RBP_ID_5491977,Human_RBP_ID_8784893,Human_RBP_ID_9278476,Human_RBP_ID_18975314,Human_RBP_ID_22436841,Human_RBP_ID_22493874,Human_RBP_ID_24996368 Human_Splice_Rec_1331956,Human_Splice_Rec_1331972,Human_Splice_Rec_1331992,Human_Splice_Rec_1332006,Human_Splice_Rec_1332020,Human_Splice_Rec_1332034,Human_Splice_Rec_1332044,Human_Splice_Rec_1332054 Human_miRNA_ID_2949249 RMVar_hsa_circ_126500,RMVar_hsa_circ_154620,RMVar_hsa_circ_154622,RMVar_hsa_circ_115443,RMVar_hsa_circ_101322,RMVar_hsa_circ_154625,RMVar_hsa_circ_90024,RMVar_hsa_circ_154624 91553 RMVar_ID_91553 Human_SNP_ID_489554617 m1A Human chr12 + 6752039 6752039 6752039 CCTGACAACATACGGCTCATATGCTGACGGTGAATAGCAAAGGGATCCCTGTGGAGTGAGCACAT CCTGACAACATACGGCTCATATGCTGACGGTGCATAGCAAAGGGATCCCTGTGGAGTGAGCACAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6751879..6752097 26863196 MeRIP-seq:(Medium) rs937523310 Functional Loss SNV dbSNP153 33..33 33 - - - 91554 RMVar_ID_91554 Human_SNP_ID_489554724 m1A Human chr12 - 6752337 6752337 6752337 TTTCCAGTGTGGAGCCCCCTGGAGCTGAGATCAGGATGTTCCGCTTCATGAGGGACGTGGAGCCT TTTCCAGTGTGGAGCCCCCTGGAGCTGAGATCGGGATGTTCCGCTTCATGAGGGACGTGGAGCCT T C MLF2 Ensembl:ENSG00000089693 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr12:6752276..6752375;chr12:6752276..6752402 26863196,32194978 MeRIP-seq:(Medium) rs141110142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426493,Human_RBP_ID_1476339,Human_RBP_ID_1799848,Human_RBP_ID_3942692,Human_RBP_ID_4238981,Human_RBP_ID_5140197,Human_RBP_ID_5314840,Human_RBP_ID_18417224,Human_RBP_ID_22435759,Human_RBP_ID_23255965,Human_RBP_ID_23571662 Human_Splice_Rec_1331954,Human_Splice_Rec_1331955,Human_Splice_Rec_1331970,Human_Splice_Rec_1331971,Human_Splice_Rec_1331990,Human_Splice_Rec_1331991,Human_Splice_Rec_1332004,Human_Splice_Rec_1332005,Human_Splice_Rec_1332018,Human_Splice_Rec_1332019,Human_Splice_Rec_1332032,Human_Splice_Rec_1332033,Human_Splice_Rec_1332042,Human_Splice_Rec_1332043,Human_Splice_Rec_1332053,Human_Splice_Rec_1332060 RMVar_hsa_circ_126500,RMVar_hsa_circ_154620,RMVar_hsa_circ_154622,RMVar_hsa_circ_115443,RMVar_hsa_circ_9097,RMVar_hsa_circ_101322,RMVar_hsa_circ_154625 91555 RMVar_ID_91555 Human_SNP_ID_489554733 m1A Human chr12 + 6752362 6752362 6752362 AACATCCTGATCTCAGCTCCAGGGGGCTCCACACTGGAAAGATATGGAAGCTCAGATACTTGGAG AACATCCTGATCTCAGCTCCAGGGGGCTCCACGCTGGAAAGATATGGAAGCTCAGATACTTGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:6752246..6752402;chr12:6752351..6752375 26863196 MeRIP-seq:(Medium) rs368161495 Functional Loss SNV dbSNP153 33..33 33 - - - 91556 RMVar_ID_91556 Human_SNP_ID_489554887 m1A Human chr12 + 6752990 6752990 6752990 AGCGGCCCATCCGGCCGGTTTCGCTTCCCGGTACGCTGCAGGGTCAGGGTCGCGGCCCGGAACGT AGCGGCCCATCCGGCCGGTTTCGCTTCCCGGTGCGCTGCAGGGTCAGGGTCGCGGCCCGGAACGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6752926..6753075 32194978 MeRIP-seq:(Medium) rs1221405607 Functional Loss SNV dbSNP153 33..33 33 - - - 91557 RMVar_ID_91557 Human_SNP_ID_489554920 m1A Human chr12 - 6753078 6753078 6753078 TCCGTTGGCCGAGGGGGCCGTACGGAGGTGGCAGCTGTGGGAGGAGGCGGCGTGGAAGGCCGAGG TCCGTTGGCCGAGGGGGCCGTACGGAGGTGGCCGCTGTGGGAGGAGGCGGCGTGGAAGGCCGAGG T G MLF2 Ensembl:ENSG00000089693 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:6752957..6753125;chr12:6752898..6753150;chr12:6752904..6753150 26863196 MeRIP-seq:(Medium) rs1290519166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33700,Human_RBP_ID_228569,Human_RBP_ID_809633,Human_RBP_ID_4238985,Human_RBP_ID_5111664,Human_RBP_ID_5314501,Human_RBP_ID_8784895,Human_RBP_ID_8940690,Human_RBP_ID_9322417,Human_RBP_ID_9340736,Human_RBP_ID_17825488,Human_RBP_ID_18975316,Human_RBP_ID_22437575,Human_RBP_ID_23125847,Human_RBP_ID_23571666,Human_RBP_ID_26768352 Human_miRNA_ID_2241561,Human_miRNA_ID_2868170 RMVar_hsa_circ_126500,RMVar_hsa_circ_154620 91558 RMVar_ID_91558 Human_SNP_ID_489554921 m1A Human chr12 + 6753082 6753082 6753082 GGCCTTCCACGCCGCCTCCTCCCACAGCTGCCACCTCCGTACGGCCCCCTCGGCCAACGGAGCCC GGCCTTCCACGCCGCCTCCTCCCACAGCTGCCGCCTCCGTACGGCCCCCTCGGCCAACGGAGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6752896..6753150 26863196 MeRIP-seq:(Medium) rs975799245 Functional Loss SNV dbSNP153 33..33 33 - - - 91559 RMVar_ID_91559 Human_SNP_ID_489558311 m1A Human chr12 - 6766277 6766277 6766277 GCTTCCCAGGGGTGGGGCAGGCGGGAGCGGGGAGGAGAGGAGAGGGGAGGGGGATGAAAGAGGAG GCTTCCCAGGGGTGGGGCAGGCGGGAGCGGGGGGGAGAGGAGAGGGGAGGGGGATGAAAGAGGAG T C MLF2 Ensembl:ENSG00000089693 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6766226..6766325 26863196 MeRIP-seq:(Medium) rs919678348 Functional Loss SNV dbSNP153 33..33 33 - - - 91560 RMVar_ID_91560 Human_SNP_ID_489558414 m1A Human chr12 + 6766510 6766510 6766510 GCCGCAGCCCTGCGGGTCTCCGCTCCAGACCCACCCCCGCCCCACCCCGCGCGCCTCTGCCGCCT GCCGCAGCCCTGCGGGTCTCCGCTCCAGACCCCCCCCCGCCCCACCCCGCGCGCCTCTGCCGCCT A C PTMS Ensembl:ENSG00000159335 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:6766351..6769094 26863196 MeRIP-seq:(Medium) rs886800784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426548,Human_RBP_ID_4245969,Human_RBP_ID_5174122,Human_RBP_ID_12013919,Human_RBP_ID_17685207,Human_RBP_ID_17825512,Human_RBP_ID_18206443,Human_RBP_ID_21918314,Human_RBP_ID_22795158,Human_RBP_ID_26614375,Human_RBP_ID_27155106,Human_RBP_ID_27217923,Human_RBP_ID_27424730 Human_miRNA_ID_652638,Human_miRNA_ID_1701802 91561 RMVar_ID_91561 Human_SNP_ID_489559196 m1A Human chr12 + 6769135 6769135 6769135 CAAAGACCTTAGAAGCTGAAGGGGAAGCTGGGAGGGATGCCCAGGAGAGAGAGTCCTCAGGAAAA CAAAGACCTTAGAAGCTGAAGGGGAAGCTGGGGGGGATGCCCAGGAGAGAGAGTCCTCAGGAAAA A G PTMS Ensembl:ENSG00000159335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6769130..6769243 26863196 MeRIP-seq:(Medium) rs955683706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1332105 91562 RMVar_ID_91562 Human_SNP_ID_489559308 m1A Human chr12 - 6769557 6769557 6769557 AGAGGTCACCTTTCTCACCACAAATGGCTTGCAGCCCCTAAGTCCCTGCAGCCCCAGTTCTCCCT AGAGGTCACCTTTCTCACCACAAATGGCTTGCTGCCCCTAAGTCCCTGCAGCCCCAGTTCTCCCT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:6769553..6769719 26863410 MeRIP-seq:(Medium) rs202102069 Functional Loss SNV dbSNP153 33..33 33 - - - 91563 RMVar_ID_91563 Human_SNP_ID_489559332 m1A Human chr12 + 6769637 6769637 6769637 CCTGAAGGAGAAGAAGGAGAAGGTGGAGGAGAAGGCAAGCCGGAAAGAGCGAAAGAAAGAAGTGG CCTGAAGGAGAAGAAGGAGAAGGTGGAGGAGAGGGCAAGCCGGAAAGAGCGAAAGAAAGAAGTGG A G PTMS Ensembl:ENSG00000159335 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6769601..6770225 26863196 MeRIP-seq:(Medium) rs746514929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36895,Human_RBP_ID_8940691,Human_RBP_ID_22039150,Human_RBP_ID_22646158,Human_RBP_ID_24543046,Human_RBP_ID_26322654 Human_Splice_Rec_1332062,Human_Splice_Rec_1332063,Human_Splice_Rec_1332070,Human_Splice_Rec_1332071,Human_Splice_Rec_1332078,Human_Splice_Rec_1332079,Human_Splice_Rec_1332086,Human_Splice_Rec_1332087,Human_Splice_Rec_1332094,Human_Splice_Rec_1332095,Human_Splice_Rec_1332098,Human_Splice_Rec_1332099,Human_Splice_Rec_1332106,Human_Splice_Rec_1332107 91564 RMVar_ID_91564 Human_SNP_ID_489559346 m1A Human chr12 - 6769670 6769670 6769670 TGTGGTCCTCTCCCCCACCCCTCCACACCTCCACCACTTCTTTCTTTCGCTCTTTCCGGCTTGCC TGTGGTCCTCTCCCCCACCCCTCCACACCTCCGCCACTTCTTTCTTTCGCTCTTTCCGGCTTGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6769601..6769675 26863196 MeRIP-seq:(Medium) rs1263253194 Functional Loss SNV dbSNP153 33..33 33 - - - 91565 RMVar_ID_91565 Human_SNP_ID_489559537 m1A Human chr12 - 6770179 6770179 6770179 TCGGCAGCTCTCTTCAGCGCGGGCCCTTCATCATCCTCTTCTTCTTCTTCCTCATCTGAGGAGCC TCGGCAGCTCTCTTCAGCGCGGGCCCTTCATCGTCCTCTTCTTCTTCTTCCTCATCTGAGGAGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:6769849..6770875 26863196 MeRIP-seq:(Medium) rs532672561 Functional Loss SNV dbSNP153 33..33 33 - - - 91566 RMVar_ID_91566 Human_SNP_ID_489559538 m1A Human chr12 - 6770179 6770179 6770179 TCGGCAGCTCTCTTCAGCGCGGGCCCTTCATCATCCTCTTCTTCTTCTTCCTCATCTGAGGAGCC TCGGCAGCTCTCTTCAGCGCGGGCCCTTCATCCTCCTCTTCTTCTTCTTCCTCATCTGAGGAGCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:6769849..6770875 26863196 MeRIP-seq:(Medium) rs532672561 Functional Loss SNV dbSNP153 33..33 33 - - - 91567 RMVar_ID_91567 Human_SNP_ID_489559552 m1A Human chr12 + 6770214 6770212 6770215 TGAAGGGCCCGCGCTGAAGAGAGCTGCCGAAGAGGAGGTTTGGGCTGGGTTGCTGGGCCTGAGGG TGAAGGGCCCGCGCTGAAGAGAGCTGCCGAA___GAGGTTTGGGCTGGGTTGCTGGGCCTGAGGG AGAG A PTMS Ensembl:ENSG00000159335 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6770176..6770250 26863196 MeRIP-seq:(Medium) rs745778378 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3605,Human_RBP_ID_194720,Human_RBP_ID_426552,Human_RBP_ID_872123,Human_RBP_ID_1479516,Human_RBP_ID_3942695,Human_RBP_ID_4248074,Human_RBP_ID_5139807,Human_RBP_ID_5170670,Human_RBP_ID_5349217,Human_RBP_ID_8229715,Human_RBP_ID_9364617,Human_RBP_ID_17669034,Human_RBP_ID_18417586,Human_RBP_ID_18469117,Human_RBP_ID_18975323,Human_RBP_ID_19057571,Human_RBP_ID_19825748,Human_RBP_ID_22040515,Human_RBP_ID_22414711,Human_RBP_ID_22645796,Human_RBP_ID_22910502,Human_RBP_ID_23113263,Human_RBP_ID_24543049,Human_RBP_ID_26320888,Human_RBP_ID_26420985,Human_RBP_ID_26768230,Human_RBP_ID_27805266 Human_Splice_Rec_1332066,Human_Splice_Rec_1332067,Human_Splice_Rec_1332074,Human_Splice_Rec_1332075,Human_Splice_Rec_1332082,Human_Splice_Rec_1332083,Human_Splice_Rec_1332090,Human_Splice_Rec_1332091,Human_Splice_Rec_1332102,Human_Splice_Rec_1332103,Human_Splice_Rec_1332110,Human_Splice_Rec_1332111 RMVar_hsa_circ_154626,RMVar_hsa_circ_95707 91568 RMVar_ID_91568 Human_SNP_ID_489577444 m1A Human chr12 + 6828910 6828910 6828910 GCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTACAACTACCTGCAGAGGGCCTATTACCAGGTGG GCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTGCAACTACCTGCAGAGGGCCTATTACCAGGTGG A G GPR162,P3H3 Ensembl:ENSG00000250510,Ensembl:ENSG00000110811 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6828656..6829039 32194978 MeRIP-seq:(Medium) rs1342391541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17685236,Human_RBP_ID_22756548 Human_Splice_Rec_1332275 91569 RMVar_ID_91569 Human_SNP_ID_489578092 m1A Human chr12 - 6830754 6830754 6830754 CCCTTCCCCAACTGACCCTGAGCATGGGCCTCATGTAGCCGCCTCAGCTGGTTGGGAAGGAAGTC CCCTTCCCCAACTGACCCTGAGCATGGGCCTCGTGTAGCCGCCTCAGCTGGTTGGGAAGGAAGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6829879..6830899 32194978 MeRIP-seq:(Medium) rs781798270 Functional Loss SNV dbSNP153 33..33 33 - - - 91570 RMVar_ID_91570 Human_SNP_ID_489579099 m1A Human chr12 + 6833970 6833970 6833970 GGAGGGTGTGACCTTGACCCAGGATTCCAGGCAGCTGAATGGGTCGGAGCGGGCGGTGTTGGATG GGAGGGTGTGACCTTGACCCAGGATTCCAGGCGGCTGAATGGGTCGGAGCGGGCGGTGTTGGATG A G P3H3 Ensembl:ENSG00000110811 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6833806..6834878 32194978 MeRIP-seq:(Medium) rs782083133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3941435,Human_RBP_ID_5347168,Human_RBP_ID_9020453,Human_RBP_ID_23118077 Human_Splice_Rec_1332290,Human_Splice_Rec_1332291,Human_Splice_Rec_1332318,Human_Splice_Rec_1332319,Human_Splice_Rec_1332354,Human_Splice_Rec_1332355,Human_Splice_Rec_1332376,Human_Splice_Rec_1332377,Human_Splice_Rec_1332386,Human_Splice_Rec_1332387,Human_Splice_Rec_1332394,Human_Splice_Rec_1332395,Human_Splice_Rec_1332405,Human_Splice_Rec_1332412,Human_Splice_Rec_1332413,Human_Splice_Rec_1332419,Human_Splice_Rec_1332422,Human_Splice_Rec_1332423 RMVar_hsa_circ_12147 91571 RMVar_ID_91571 Human_SNP_ID_489582486 m1A Human chr12 + 6844898 6844898 6844898 AAGTACTTCCCGAAACAAAGCCCTTCTGTAGCATAATCACTGTATGATTCTTAAGATCAGGAAAC AAGTACTTCCCGAAACAAAGCCCTTCTGTAGCGTAATCACTGTATGATTCTTAAGATCAGGAAAC A G GNB3 Ensembl:ENSG00000111664 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6844887..6844958 26863196 MeRIP-seq:(Medium) rs113904241 Functional Loss SNV dbSNP153 33..33 33 - - - 91572 RMVar_ID_91572 Human_SNP_ID_489582661 m1A Human chr12 - 6845589 6845589 6845589 CGAGCCCGTGCAGATGGCCTCTCCATTGGGGAAGAACTGAGGGCACGGGTGGCAAGTGGGTCAGG CGAGCCCGTGCAGATGGCCTCTCCATTGGGGAGGAACTGAGGGCACGGGTGGCAAGTGGGTCAGG T C CDCA3 Ensembl:ENSG00000111665 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6843920..6845658 32194978 MeRIP-seq:(Medium) rs782066777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17825729 91573 RMVar_ID_91573 Human_SNP_ID_489583055 m1A Human chr12 - 6846890 6846890 6846890 TCCACTTCCCTTTCTCCAGCCTCCTCAGTTCCAGATTTTGAGGAAGCTGTCCCAGGAACCTGTGG TCCACTTCCCTTTCTCCAGCCTCCTCAGTTCCGGATTTTGAGGAAGCTGTCCCAGGAACCTGTGG T C CDCA3 Ensembl:ENSG00000111665 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6846794..6846895 32194978 MeRIP-seq:(Medium) rs1555124870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18976756,Human_RBP_ID_22908489 Human_Splice_Rec_1332546,Human_Splice_Rec_1332548,Human_Splice_Rec_1332550 91574 RMVar_ID_91574 Human_SNP_ID_489584060 m1A Human chr12 - 6850923 6850923 6850923 GAGATGGGCTCAGCCAAGAGCGTCCCAGTCACACCAGCGCGGCCTCCGCCGCACAACAAGCATCT GAGATGGGCTCAGCCAAGAGCGTCCCAGTCACGCCAGCGCGGCCTCCGCCGCACAACAAGCATCT T C CDCA3 Ensembl:ENSG00000111665 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6850872..6851025 26863196 MeRIP-seq:(Medium) rs782623630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1476616,Human_RBP_ID_4239599 Human_Splice_Rec_1332540,Human_Splice_Rec_1332541,Human_Splice_Rec_1332554,Human_Splice_Rec_1332555,Human_Splice_Rec_1332564,Human_Splice_Rec_1332565,Human_Splice_Rec_1332573,Human_Splice_Rec_1332582,Human_Splice_Rec_1332588,Human_Splice_Rec_1332589,Human_Splice_Rec_1332608,Human_Splice_Rec_1332609 RMVar_hsa_circ_30228 91575 RMVar_ID_91575 Human_SNP_ID_489584072 m1A Human chr12 - 6850973 6850973 6850973 TCCCTCCTCGTCCCGGGCTGGCCCTTGCCCCCACCCTGCAACTCCTGGTTGAGATGGGCTCAGCC TCCCTCCTCGTCCCGGGCTGGCCCTTGCCCCCTCCCTGCAACTCCTGGTTGAGATGGGCTCAGCC T A CDCA3 Ensembl:ENSG00000111665 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6850926..6851000 32194978 MeRIP-seq:(Medium) rs782421614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247251,Human_RBP_ID_5111384,Human_RBP_ID_5437998,Human_RBP_ID_5492000,Human_RBP_ID_8382621,Human_RBP_ID_23207969 Human_Splice_Rec_1332540,Human_Splice_Rec_1332554,Human_Splice_Rec_1332564,Human_Splice_Rec_1332582,Human_Splice_Rec_1332588,Human_Splice_Rec_1332608 RMVar_hsa_circ_30228 91576 RMVar_ID_91576 Human_SNP_ID_489584113 m1A Human chr12 - 6851077 6851077 6851077 CAGGAAGTTTCTTCACTGGAAACTGGGAAGACAGGGTGGTTTAGGGTTGAAGGTCCGACGTGGAA CAGGAAGTTTCTTCACTGGAAACTGGGAAGACGGGGTGGTTTAGGGTTGAAGGTCCGACGTGGAA T C CDCA3 Ensembl:ENSG00000111665 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6851073..6851275 26863196 MeRIP-seq:(Medium) rs1555126430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3412755,Human_RBP_ID_4239603,Human_RBP_ID_17825750,Human_RBP_ID_22039154 91577 RMVar_ID_91577 Human_SNP_ID_489585296 m1A Human chr12 - 6855500 6855500 6855500 TCCTACCGGGCGCCGGGTCCGCCGGAGGTGCAAGTAGACTCGCTGGCCGGTCTTATTGAAATGTC TCCTACCGGGCGCCGGGTCCGCCGGAGGTGCAGGTAGACTCGCTGGCCGGTCTTATTGAAATGTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:6855451..6855550;chr12:6855401..6855613 26863196 MeRIP-seq:(Medium) rs782711495 Functional Loss SNV dbSNP153 33..33 33 - - - 91578 RMVar_ID_91578 Human_SNP_ID_489585462 m1A Human chr12 - 6856001 6856001 6856001 AAATCCGCCTTCAACACCTGGAAGGATAGGGAAGAAGAGGGAGAGTAGAGCAATGACAACAGGTC AAATCCGCCTTCAACACCTGGAAGGATAGGGAGGAAGAGGGAGAGTAGAGCAATGACAACAGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6855997..6856175 26863196 MeRIP-seq:(Medium) rs1565529785 Functional Loss SNV dbSNP153 33..33 33 - - - 91579 RMVar_ID_91579 Human_SNP_ID_489585463 m1A Human chr12 - 6856002 6856002 6856002 CAAATCCGCCTTCAACACCTGGAAGGATAGGGAAGAAGAGGGAGAGTAGAGCAATGACAACAGGT CAAATCCGCCTTCAACACCTGGAAGGATAGGGTAGAAGAGGGAGAGTAGAGCAATGACAACAGGT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6856001..6856075 26863196 MeRIP-seq:(Medium) rs1555128134 Functional Loss SNV dbSNP153 33..33 33 - - - 91580 RMVar_ID_91580 Human_SNP_ID_489585719 m1A Human chr12 - 6856797 6856797 6856797 TGCTCCACAGCGTGGTTGTTGCCCCCACTGCCATCGAAGTAGCGTCGCCCACAGAGGATGGAGCC TGCTCCACAGCGTGGTTGTTGCCCCCACTGCCGTCGAAGTAGCGTCGCCCACAGAGGATGGAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6856685..6856851 26863196 MeRIP-seq:(Medium) rs781924172 Functional Loss SNV dbSNP153 33..33 33 - - - 91581 RMVar_ID_91581 Human_SNP_ID_489587701 m1A Human chr12 - 6864120 6864120 6864120 ATGGAGACAATGGTGGTCACACAGTCCTCAGGAGGGGGGTCGGCTGCTGCGCTTGTGGAGCCCGG ATGGAGACAATGGTGGTCACACAGTCCTCAGGGGGGGGGTCGGCTGCTGCGCTTGTGGAGCCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6864070..6864222 26863196 MeRIP-seq:(Medium) rs1555130203 Functional Loss SNV dbSNP153 33..33 33 - - - 91582 RMVar_ID_91582 Human_SNP_ID_489588831 m1A Human chr12 + 6867599 6867599 6867599 ATGGCGCCCTCCAGGAAGTTCTTCGTTGGGGGAAACTGGAAGATGAACGGGCGGAAGCAGAGTCT ATGGCGCCCTCCAGGAAGTTCTTCGTTGGGGGGAACTGGAAGATGAACGGGCGGAAGCAGAGTCT A G TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6867551..6867600 26863196 MeRIP-seq:(Medium) rs782672720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34280,Human_RBP_ID_427090,Human_RBP_ID_753411,Human_RBP_ID_810737,Human_RBP_ID_876688,Human_RBP_ID_1270490,Human_RBP_ID_1476976,Human_RBP_ID_1800568,Human_RBP_ID_3413021,Human_RBP_ID_4239945,Human_RBP_ID_5314505,Human_RBP_ID_5492016,Human_RBP_ID_5555675,Human_RBP_ID_6215163,Human_RBP_ID_8382874,Human_RBP_ID_8785119,Human_RBP_ID_17240415,Human_RBP_ID_17473407,Human_RBP_ID_18632719,Human_RBP_ID_22435766,Human_RBP_ID_22574089,Human_RBP_ID_22908708,Human_RBP_ID_23125855,Human_RBP_ID_23572582,Human_RBP_ID_26419507,Human_RBP_ID_26911266,Human_RBP_ID_27154995,Human_RBP_ID_27218130 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2070666,Human_miRNA_ID_2803586 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91583 RMVar_ID_91583 Human_SNP_ID_489588842 m1A Human chr12 + 6867625 6867624 6867626 TGGGGGAAACTGGAAGATGAACGGGCGGAAGCAGAGTCTGGGGGAGCTCATCGGCACTCTGAACG TGGGGGAAACTGGAAGATGAACGGGCGGAAGC__AGTCTGGGGGAGCTCATCGGCACTCTGAACG CAG C TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6867574..6867742 26863196 MeRIP-seq:(Medium) rs782447245 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_34280,Human_RBP_ID_228795,Human_RBP_ID_427092,Human_RBP_ID_753411,Human_RBP_ID_810737,Human_RBP_ID_876688,Human_RBP_ID_1476976,Human_RBP_ID_1800569,Human_RBP_ID_3413021,Human_RBP_ID_4239945,Human_RBP_ID_5170565,Human_RBP_ID_5314505,Human_RBP_ID_6215163,Human_RBP_ID_8382875,Human_RBP_ID_12021118,Human_RBP_ID_17240415,Human_RBP_ID_18632719,Human_RBP_ID_22435766,Human_RBP_ID_22493914,Human_RBP_ID_22574089,Human_RBP_ID_23125855,Human_RBP_ID_26911266,Human_RBP_ID_27218130,Human_RBP_ID_27424861 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2469162,Human_miRNA_ID_2894274 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91584 RMVar_ID_91584 Human_SNP_ID_489588844 m1A Human chr12 + 6867625 6867625 6867625 TGGGGGAAACTGGAAGATGAACGGGCGGAAGCAGAGTCTGGGGGAGCTCATCGGCACTCTGAACG TGGGGGAAACTGGAAGATGAACGGGCGGAAGCGGAGTCTGGGGGAGCTCATCGGCACTCTGAACG A G TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6867574..6867742 26863196 MeRIP-seq:(Medium) rs1555131539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34280,Human_RBP_ID_228795,Human_RBP_ID_427092,Human_RBP_ID_753411,Human_RBP_ID_810737,Human_RBP_ID_876688,Human_RBP_ID_1476976,Human_RBP_ID_1800569,Human_RBP_ID_3413021,Human_RBP_ID_4239945,Human_RBP_ID_5170565,Human_RBP_ID_5314505,Human_RBP_ID_6215163,Human_RBP_ID_8382875,Human_RBP_ID_12021118,Human_RBP_ID_17240415,Human_RBP_ID_18632719,Human_RBP_ID_22435766,Human_RBP_ID_22493914,Human_RBP_ID_22574089,Human_RBP_ID_23125855,Human_RBP_ID_26911266,Human_RBP_ID_27218130,Human_RBP_ID_27424861 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2469162,Human_miRNA_ID_2894274 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91585 RMVar_ID_91585 Human_SNP_ID_489588852 m1A Human chr12 + 6867642 6867642 6867642 TGAACGGGCGGAAGCAGAGTCTGGGGGAGCTCATCGGCACTCTGAACGCGGCCAAGGTGCCGGCC TGAACGGGCGGAAGCAGAGTCTGGGGGAGCTCGTCGGCACTCTGAACGCGGCCAAGGTGCCGGCC A G TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6867551..6867641 26863196 MeRIP-seq:(Medium) rs1555131553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34280,Human_RBP_ID_228795,Human_RBP_ID_810737,Human_RBP_ID_876688,Human_RBP_ID_994276,Human_RBP_ID_1476976,Human_RBP_ID_1800569,Human_RBP_ID_4239945,Human_RBP_ID_5170566,Human_RBP_ID_5314505,Human_RBP_ID_6215163,Human_RBP_ID_12021119,Human_RBP_ID_18632720,Human_RBP_ID_22435766,Human_RBP_ID_22493915,Human_RBP_ID_22574089,Human_RBP_ID_23125855,Human_RBP_ID_27154996,Human_RBP_ID_27424861 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2218026,Human_miRNA_ID_2515816,Human_miRNA_ID_2894274 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91586 RMVar_ID_91586 Human_SNP_ID_489588856 m1A Human chr12 + 6867648 6867648 6867648 GGCGGAAGCAGAGTCTGGGGGAGCTCATCGGCACTCTGAACGCGGCCAAGGTGCCGGCCGACACC GGCGGAAGCAGAGTCTGGGGGAGCTCATCGGCTCTCTGAACGCGGCCAAGGTGCCGGCCGACACC A T TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Normoxia chr12:6867551..6867785;chr12:6867568..6868137 26863196,32194978 MeRIP-seq:(Medium) rs1565536608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34280,Human_RBP_ID_228795,Human_RBP_ID_876688,Human_RBP_ID_994276,Human_RBP_ID_1476976,Human_RBP_ID_1800569,Human_RBP_ID_4239945,Human_RBP_ID_5170566,Human_RBP_ID_5314505,Human_RBP_ID_6215163,Human_RBP_ID_12021119,Human_RBP_ID_22435766,Human_RBP_ID_22574089,Human_RBP_ID_27154996,Human_RBP_ID_27424861 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2218026,Human_miRNA_ID_2515816 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91587 RMVar_ID_91587 Human_SNP_ID_489588859 m1A Human chr12 + 6867654 6867654 6867654 AGCAGAGTCTGGGGGAGCTCATCGGCACTCTGAACGCGGCCAAGGTGCCGGCCGACACCGGTAAG AGCAGAGTCTGGGGGAGCTCATCGGCACTCTGCACGCGGCCAAGGTGCCGGCCGACACCGGTAAG A C TPI1 Ensembl:ENSG00000111669 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:6867556..6867655 26863410 MeRIP-seq:(Medium) rs1555131560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228795,Human_RBP_ID_876688,Human_RBP_ID_1476977,Human_RBP_ID_1800569,Human_RBP_ID_4239945,Human_RBP_ID_5170566,Human_RBP_ID_5314505,Human_RBP_ID_22435766,Human_RBP_ID_27424861 Human_Splice_Rec_1332743,Human_Splice_Rec_1332755,Human_Splice_Rec_1332767 Human_miRNA_ID_2218026 RMVar_hsa_circ_108613,RMVar_hsa_circ_154646 91588 RMVar_ID_91588 Human_SNP_ID_489589301 m1A Human chr12 + 6868813 6868813 6868813 GGGCTCCAGGGCACTGGTTAGGAATTGTGGGGAATGAAGGCTTTCTTTAGTCTCATCCCCCTGTG GGGCTCCAGGGCACTGGTTAGGAATTGTGGGGGATGAAGGCTTTCTTTAGTCTCATCCCCCTGTG A G TPI1 Ensembl:ENSG00000111669 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6868808..6868922 26863196 MeRIP-seq:(Medium) rs1390195420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810741,Human_RBP_ID_874222,Human_RBP_ID_5172040,Human_RBP_ID_5346443,Human_RBP_ID_9416385,Human_RBP_ID_22574090,Human_RBP_ID_22644597,Human_RBP_ID_22908719,Human_RBP_ID_23269761,Human_RBP_ID_24551199,Human_RBP_ID_26776774 RMVar_hsa_circ_108613,RMVar_hsa_circ_84123,RMVar_hsa_circ_154646,RMVar_hsa_circ_154647 91589 RMVar_ID_91589 Human_SNP_ID_489589520 m1A Human chr12 - 6869328 6869328 6869328 CCTTCTCAGTGATGCCAGCTTCCCTTTCATCTAGCTTCTCCCCAATGCAGGCGATTACTCCGAGT CCTTCTCAGTGATGCCAGCTTCCCTTTCATCTGGCTTCTCCCCAATGCAGGCGATTACTCCGAGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6869326..6869350 26863196 MeRIP-seq:(Medium) rs896916107 Functional Loss SNV dbSNP153 33..33 33 - - - 91590 RMVar_ID_91590 Human_SNP_ID_489589664 m1A Human chr12 - 6869749 6869749 6869749 CCGGTTACCTGTTGGGGTGTTGCAGTCTTGCCAGTACCAATGGCCCACACAGGCTCATAGGCCAG CCGGTTACCTGTTGGGGTGTTGCAGTCTTGCCGGTACCAATGGCCCACACAGGCTCATAGGCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6869726..6869750 26863196 MeRIP-seq:(Medium) rs782225455 Functional Loss SNV dbSNP153 33..33 33 - - - 91591 RMVar_ID_91591 Human_SNP_ID_489589742 m1A Human chr12 + 6870007 6870004 6870008 TGTCCACTGGTGCCAGTGATTTTTCCTCTTAGAGAGGCAGAAAAGGTCTTACTTAGGCCAGCTTC TGTCCACTGGTGCCAGTGATTTTTCCTCTT____AGGCAGAAAAGGTCTTACTTAGGCCAGCTTC TAGAG T TPI1 Ensembl:ENSG00000111669 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6870005..6870122 26863196 MeRIP-seq:(Medium) rs782474817 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_22338,RMVar_hsa_circ_86111,RMVar_hsa_circ_82301,RMVar_hsa_circ_154648,RMVar_hsa_circ_154650,RMVar_hsa_circ_154654,RMVar_hsa_circ_329941,RMVar_hsa_circ_94648,RMVar_hsa_circ_154653 91592 RMVar_ID_91592 Human_SNP_ID_489589745 m1A Human chr12 + 6870007 6870007 6870007 TGTCCACTGGTGCCAGTGATTTTTCCTCTTAGAGAGGCAGAAAAGGTCTTACTTAGGCCAGCTTC TGTCCACTGGTGCCAGTGATTTTTCCTCTTAGCGAGGCAGAAAAGGTCTTACTTAGGCCAGCTTC A C TPI1 Ensembl:ENSG00000111669 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6870005..6870122 26863196 MeRIP-seq:(Medium) rs1555132463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22338,RMVar_hsa_circ_86111,RMVar_hsa_circ_82301,RMVar_hsa_circ_154648,RMVar_hsa_circ_154650,RMVar_hsa_circ_154654,RMVar_hsa_circ_329941,RMVar_hsa_circ_94648,RMVar_hsa_circ_154653 91593 RMVar_ID_91593 Human_SNP_ID_489589930 m1A Human chr12 - 6870460 6870460 6870460 AAGGAGCAGATGACACCATCAGAAGCATATGCAGGGAAAGGGCAGTTACTGGGCTTCTGGGCTGC AAGGAGCAGATGACACCATCAGAAGCATATGCGGGGAAAGGGCAGTTACTGGGCTTCTGGGCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6870401..6870764 26863196 MeRIP-seq:(Medium) rs782490594 Functional Loss SNV dbSNP153 33..33 33 - - - 91594 RMVar_ID_91594 Human_SNP_ID_489589943 m1A Human chr12 - 6870485 6870485 6870485 GATACAGTTTGGATGAGGCCACAGGAAGGAGCAGATGACACCATCAGAAGCATATGCAGGGAAAG GATACAGTTTGGATGAGGCCACAGGAAGGAGCGGATGACACCATCAGAAGCATATGCAGGGAAAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr12:6870435..6870563;chr12:6870435..6870520 26863196 MeRIP-seq:(Medium) rs782684621 Functional Loss SNV dbSNP153 33..33 33 - - - 91595 RMVar_ID_91595 Human_SNP_ID_489599744 m1A Human chr12 + 6904874 6904874 6904874 AAAGTGGCGTGGTAACCAGGCAACTACTGATCAATCCCCTCCCCGGCTGATTTGCGCATCAGGTA AAAGTGGCGTGGTAACCAGGCAACTACTGATCTATCCCCTCCCCGGCTGATTTGCGCATCAGGTA A T LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6904853..6904969 26863196 MeRIP-seq:(Medium) rs929009998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1332879,Human_Splice_Rec_1332893,Human_Splice_Rec_1332901,Human_Splice_Rec_1332927,Human_Splice_Rec_1332935,Human_Splice_Rec_1332951 91596 RMVar_ID_91596 Human_SNP_ID_489603319 m1A Human chr12 - 6915537 6915537 6915537 ATGAGATGGGAGAACACTGCAGTGAGGAGGGGAGGGGCACGACAGTGGTTCCCGCGCCTCTTTGC ATGAGATGGGAGAACACTGCAGTGAGGAGGGGTGGGGCACGACAGTGGTTCCCGCGCCTCTTTGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6915531..6915683 32194978 MeRIP-seq:(Medium) rs1332742530 Functional Loss SNV dbSNP153 33..33 33 - - - 91597 RMVar_ID_91597 Human_SNP_ID_489603594 m1A Human chr12 - 6916477 6916477 6916477 TGCCTAAGTAACGCTGTTTGTCTCCATCCCTCAGCTCCAGGGCCTCATAGATGCCCGTAGAGGCT TGCCTAAGTAACGCTGTTTGTCTCCATCCCTCGGCTCCAGGGCCTCATAGATGCCCGTAGAGGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6915776..6916569 32194978 MeRIP-seq:(Medium) rs1194338739 Functional Loss SNV dbSNP153 33..33 33 - - - 91598 RMVar_ID_91598 Human_SNP_ID_489604064 m1A Human chr12 - 6917960 6917960 6917960 TGCATGGCCAGCTTGTTGCCAGCATGAGAGCCACCATTGATCACGTTGAAGGCCTGGGGAGCCAC TGCATGGCCAGCTTGTTGCCAGCATGAGAGCCGCCATTGATCACGTTGAAGGCCTGGGGAGCCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6917576..6918175 32194978 MeRIP-seq:(Medium) rs782297180 Functional Loss SNV dbSNP153 33..33 33 - - - 91599 RMVar_ID_91599 Human_SNP_ID_489605567 m1A Human chr12 + 6923575 6923532 6923576 GAGTTTTCCTCTATACATCTCTCCCCAACCCTAGGTTCCCTGTTCTTCCTCCAGCTGCACCAGAG __________________________________GTTCCCTGTTCTTCCTCCAGCTGCACCAGAG TGTGCCTGGGGGAGTTTTCCTCTATACATCTCTCCCCAACCCTAG T ENO2 Ensembl:ENSG00000111674 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6923526..6923600 32194978 MeRIP-seq:(Medium) rs1392002204 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_427343,Human_RBP_ID_6216765,Human_RBP_ID_17685279,Human_RBP_ID_17826130,Human_RBP_ID_23207981,Human_RBP_ID_26420995 RMVar_hsa_circ_126108,RMVar_hsa_circ_154659 91600 RMVar_ID_91600 Human_SNP_ID_489606436 m1A Human chr12 + 6926722 6926722 6926722 CTTGAACTCCTGACAAGTGACCCACCCGACTCAGCCTCCGAAAGTGCTGAGATTACAGGCGTGAG CTTGAACTCCTGACAAGTGACCCACCCGACTCGGCCTCCGAAAGTGCTGAGATTACAGGCGTGAG A G ATN1 Ensembl:ENSG00000111676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6926718..6926841 26863196 MeRIP-seq:(Medium) rs1383122773 Functional Loss SNV dbSNP153 33..33 33 - - - 91601 RMVar_ID_91601 Human_SNP_ID_489606495 m1A Human chr12 - 6926937 6926937 6926937 GAAAGAAGGGTGGGAGACACCGGGCTGGCTGGATCCTGGGGGTGGGGGCTCCCAGTAGAGCCGAG GAAAGAAGGGTGGGAGACACCGGGCTGGCTGGGTCCTGGGGGTGGGGGCTCCCAGTAGAGCCGAG T C HSALNG0088942 RNACentral:URS0000E94606 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6926927..6927121 26863196 MeRIP-seq:(Medium) rs977535196 Functional Loss SNV dbSNP153 33..33 33 - - - 91602 RMVar_ID_91602 Human_SNP_ID_489606514 m1A Human chr12 + 6927012 6927012 6927012 CCCTCCTTTCTCACCCAGAACCTATTTTCCCTAGAATTGGCACCTGGGCCCACCTCGTTCATCCC CCCTCCTTTCTCACCCAGAACCTATTTTCCCTGGAATTGGCACCTGGGCCCACCTCGTTCATCCC A G ATN1 Ensembl:ENSG00000111676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6926979..6927131 26863196 MeRIP-seq:(Medium) rs1409851685 Functional Loss SNV dbSNP153 33..33 33 - - - 91603 RMVar_ID_91603 Human_SNP_ID_489606573 m1A Human chr12 - 6927250 6927250 6927250 CAGAGAGAATGGGATGGAAGTTTGGGGTCATAAGGAGAGAGAAAAATTGAAAAGATGACATATAT CAGAGAGAATGGGATGGAAGTTTGGGGTCATATGGAGAGAGAAAAATTGAAAAGATGACATATAT T A HSALNG0088942 RNACentral:URS0000E94606 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6927249..6927411 26863196 MeRIP-seq:(Medium) rs1555142663 Functional Loss SNV dbSNP153 33..33 33 - - - 91604 RMVar_ID_91604 Human_SNP_ID_489606704 m1A Human chr12 - 6927674 6927674 6927674 AGGAGGGAGACGCGAGGGAGGGAGCGCGAGGCAAGCCGCGAGGGGGGAGAGAGGGGGAGCCGGAG AGGAGGGAGACGCGAGGGAGGGAGCGCGAGGCCAGCCGCGAGGGGGGAGAGAGGGGGAGCCGGAG T G HSALNG0088942 RNACentral:URS0000E94606 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:6927545..6927759 26863410 MeRIP-seq:(Medium) rs1430684320 Functional Loss SNV dbSNP153 33..33 33 - - - 91605 RMVar_ID_91605 Human_SNP_ID_489606812 m1A Human chr12 - 6928030 6928030 6928030 CCGCGGCCCGCCCGGCCCTCGGCGCGGTTCCGACCCGCCGCCGCCCGCGCCCGCCTAGCGCAGCC CCGCGGCCCGCCCGGCCCTCGGCGCGGTTCCGGCCCGCCGCCGCCCGCGCCCGCCTAGCGCAGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:6927722..6928200 26863196 MeRIP-seq:(Medium) rs1326439445 Functional Loss SNV dbSNP153 33..33 33 - - - 91606 RMVar_ID_91606 Human_SNP_ID_489606818 m1A Human chr12 + 6928044 6928044 6928044 GGCGCGGGCGGCGGCGGGTCGGAACCGCGCCGAGGGCCGGGCGGGCCGCGGGGCCGGGCGGCGCG GGCGCGGGCGGCGGCGGGTCGGAACCGCGCCGGGGGCCGGGCGGGCCGCGGGGCCGGGCGGCGCG A G ATN1 Ensembl:ENSG00000111676 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr12:6927558..6928325;chr12:6927701..6928225 26863196 MeRIP-seq:(Medium) rs1362998032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229857,Human_RBP_ID_259861,Human_RBP_ID_3418904,Human_RBP_ID_5314508,Human_RBP_ID_8177326,Human_RBP_ID_8725406,Human_RBP_ID_9322428,Human_RBP_ID_9352747,Human_RBP_ID_9416387,Human_RBP_ID_19055882,Human_RBP_ID_21966987,Human_RBP_ID_26776780 91607 RMVar_ID_91607 Human_SNP_ID_489606819 m1A Human chr12 + 6928044 6928044 6928044 GGCGCGGGCGGCGGCGGGTCGGAACCGCGCCGAGGGCCGGGCGGGCCGCGGGGCCGGGCGGCGCG GGCGCGGGCGGCGGCGGGTCGGAACCGCGCCGTGGGCCGGGCGGGCCGCGGGGCCGGGCGGCGCG A T ATN1 Ensembl:ENSG00000111676 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr12:6927558..6928325;chr12:6927701..6928225 26863196 MeRIP-seq:(Medium) rs1362998032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229857,Human_RBP_ID_259861,Human_RBP_ID_3418904,Human_RBP_ID_5314508,Human_RBP_ID_8177326,Human_RBP_ID_8725406,Human_RBP_ID_9322428,Human_RBP_ID_9352747,Human_RBP_ID_9416387,Human_RBP_ID_19055882,Human_RBP_ID_21966987,Human_RBP_ID_26776780 91608 RMVar_ID_91608 Human_SNP_ID_489606844 m1A Human chr12 + 6928104 6928104 6928104 GCGCGGCGGGGGCGGGCGGCGCGGCCCGGGGCATTCCGGGCGGCCAGGGGGAGGCGGCGAGCCCG GCGCGGCGGGGGCGGGCGGCGCGGCCCGGGGCGTTCCGGGCGGCCAGGGGGAGGCGGCGAGCCCG A G ATN1 Ensembl:ENSG00000111676 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:6927951..6928146 26863410 MeRIP-seq:(Medium) rs1463371854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259861,Human_RBP_ID_3418904,Human_RBP_ID_3941451,Human_RBP_ID_4240337,Human_RBP_ID_5139551,Human_RBP_ID_5170676,Human_RBP_ID_5314508,Human_RBP_ID_5492030,Human_RBP_ID_8177326,Human_RBP_ID_8229718,Human_RBP_ID_9322428,Human_RBP_ID_9352747,Human_RBP_ID_9416056,Human_RBP_ID_17067334,Human_RBP_ID_18417398,Human_RBP_ID_19055882,Human_RBP_ID_21966987,Human_RBP_ID_22435779,Human_RBP_ID_22532475,Human_RBP_ID_26321183,Human_RBP_ID_26777234 91609 RMVar_ID_91609 Human_SNP_ID_489608896 m1A Human chr12 - 6935825 6935825 6935825 GGAGCATGATATCCAGTGGGTGTCACAGAAGGATGGGGTTCAAAGCTAGCCTCTGGCTGTCGAGG GGAGCATGATATCCAGTGGGTGTCACAGAAGGGTGGGGTTCAAAGCTAGCCTCTGGCTGTCGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:6935548..6935950;chr12:6935676..6935912 26863196 MeRIP-seq:(Medium) rs1245963888 Functional Loss SNV dbSNP153 33..33 33 - - - 91610 RMVar_ID_91610 Human_SNP_ID_489609156 m1A Human chr12 + 6936419 6936419 6936419 CCTTATTCATCCTCTAGTAGTAGCTCTGCAGCAGCCTCCTCTTCCAGTTCTTCCTCCTCTTCCTC CCTTATTCATCCTCTAGTAGTAGCTCTGCAGCGGCCTCCTCTTCCAGTTCTTCCTCCTCTTCCTC A G ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6936051..6936725 26863196 MeRIP-seq:(Medium) rs1334254107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427363,Human_RBP_ID_5127076,Human_RBP_ID_6216801,Human_RBP_ID_8383103,Human_RBP_ID_12024470,Human_RBP_ID_18632951,Human_RBP_ID_18935050 Human_miRNA_ID_1035022,Human_miRNA_ID_1384478 RMVar_hsa_circ_64732 91611 RMVar_ID_91611 Human_SNP_ID_489609185 m1A Human chr12 - 6936470 6936466 6936471 AAAGAGTGGGGGTAGCTGGGCAATGCCTGGGAAGCTGGGAAGGGGGAGGCAGAGGAAGAGGAGGA AAAGAGTGGGGGTAGCTGGGCAATGCCTGGG_____GGGAAGGGGGAGGCAGAGGAAGAGGAGGA CAGCTT C lnc-PHB2-7 RNACentral:URS0000D570C4 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6936419..6936638 26863196 MeRIP-seq:(Medium) rs782686941 Functional Loss DEL dbSNP153 32..36 33 - - - 91612 RMVar_ID_91612 Human_SNP_ID_489609188 m1A Human chr12 - 6936470 6936470 6936470 AAAGAGTGGGGGTAGCTGGGCAATGCCTGGGAAGCTGGGAAGGGGGAGGCAGAGGAAGAGGAGGA AAAGAGTGGGGGTAGCTGGGCAATGCCTGGGAGGCTGGGAAGGGGGAGGCAGAGGAAGAGGAGGA T C lnc-PHB2-7 RNACentral:URS0000D570C4 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6936419..6936638 26863196 MeRIP-seq:(Medium) rs1555143680 Functional Loss SNV dbSNP153 33..33 33 - - - 91613 RMVar_ID_91613 Human_SNP_ID_489609233 m1A Human chr12 + 6936599 6936599 6936599 TCCCAGGCTGTGTGGAGCCAGGGTCCCCCACCACCTCCTCCCTATGGCCGCCTCTTAGCCAACAG TCCCAGGCTGTGTGGAGCCAGGGTCCCCCACCTCCTCCTCCCTATGGCCGCCTCTTAGCCAACAG A T ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6936051..6937627 26863196 MeRIP-seq:(Medium) rs1162931528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755589,Human_RBP_ID_3418254,Human_RBP_ID_5126812,Human_RBP_ID_5314858,Human_RBP_ID_17074785,Human_RBP_ID_17243091,Human_RBP_ID_17357514,Human_RBP_ID_17650601,Human_RBP_ID_18934283,Human_RBP_ID_19824501 Human_miRNA_ID_1321335,Human_miRNA_ID_1364335,Human_miRNA_ID_1384479 RMVar_hsa_circ_64732 91614 RMVar_ID_91614 Human_SNP_ID_489609614 m1A Human chr12 - 6936989 6936989 6936989 CATGGGTAGGACCCTTGAGAAGTGGAAGAGGAAGAGTTGGAAGAGGAAGAGACTGGAGGGCCATT CATGGGTAGGACCCTTGAGAAGTGGAAGAGGAGGAGTTGGAAGAGGAAGAGACTGGAGGGCCATT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:6936795..6937141 26863196 MeRIP-seq:(Medium) rs1425701669 Functional Loss SNV dbSNP153 33..33 33 - - - 91615 RMVar_ID_91615 Human_SNP_ID_489609811 m1A Human chr12 + 6937394 6937394 6937394 CCTGCGGGGCCCTCAGGCCTGCCATCGCTGCCACCACCACCTGCGGCCCCTGCCTCAGGGCCGCC CCTGCGGGGCCCTCAGGCCTGCCATCGCTGCCGCCACCACCTGCGGCCCCTGCCTCAGGGCCGCC A G ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6937344..6937525 26863196 MeRIP-seq:(Medium) rs1555143965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9366126,Human_RBP_ID_18469125,Human_RBP_ID_19806051,Human_RBP_ID_22039160 RMVar_hsa_circ_64732 91616 RMVar_ID_91616 Human_SNP_ID_489609871 m1A Human chr12 - 6937525 6937525 6937525 CAGACTGACTGGCATGGCTGGGTACATCTACCACCTTGGGAGGGGGCGAGGGGCTGCGGGCTGGG CAGACTGACTGGCATGGCTGGGTACATCTACCGCCTTGGGAGGGGGCGAGGGGCTGCGGGCTGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6937501..6937525 26863196 MeRIP-seq:(Medium) rs1565567743 Functional Loss SNV dbSNP153 33..33 33 - - - 91617 RMVar_ID_91617 Human_SNP_ID_489610059 m1A Human chr12 + 6937954 6937954 6937954 AGCTGGCCAAGAAGCGGGCCGACCTGGTGGAGAAGGTGCGGCGCGAGGCCGAGCAGCGCGCGCGC AGCTGGCCAAGAAGCGGGCCGACCTGGTGGAGGAGGTGCGGCGCGAGGCCGAGCAGCGCGCGCGC A G ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6937826..6938038 26863196 MeRIP-seq:(Medium) rs1555144095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3203,Human_RBP_ID_9366127,Human_RBP_ID_18976794,Human_RBP_ID_26323834,Human_RBP_ID_27805276 RMVar_hsa_circ_64732 91618 RMVar_ID_91618 Human_SNP_ID_489610391 m1A Human chr12 - 6938750 6938750 6938750 CGTTCACGGGCTTCCCGTTCCCTCTCCCGGGCAGCTGGATCACTGCTGTACAGGGCCGGGACATT CGTTCACGGGCTTCCCGTTCCCTCTCCCGGGCTGCTGGATCACTGCTGTACAGGGCCGGGACATT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6938701..6938807 26863196 MeRIP-seq:(Medium) rs782213823 Functional Loss SNV dbSNP153 33..33 33 - - - 91619 RMVar_ID_91619 Human_SNP_ID_489610392 m1A Human chr12 - 6938750 6938750 6938750 CGTTCACGGGCTTCCCGTTCCCTCTCCCGGGCAGCTGGATCACTGCTGTACAGGGCCGGGACATT CGTTCACGGGCTTCCCGTTCCCTCTCCCGGGCGGCTGGATCACTGCTGTACAGGGCCGGGACATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6938701..6938807 26863196 MeRIP-seq:(Medium) rs782213823 Functional Loss SNV dbSNP153 33..33 33 - - - 91620 RMVar_ID_91620 Human_SNP_ID_489610464 m1A Human chr12 - 6938956 6938956 6938956 GCCCAGCTGCCAGCGCTAGACGTTCTCGCTCCAGGGGCCCCAGGCTCGGATGAAAGGGGAAAGGG GCCCAGCTGCCAGCGCTAGACGTTCTCGCTCCGGGGGCCCCAGGCTCGGATGAAAGGGGAAAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6938906..6939180 26863196 MeRIP-seq:(Medium) rs781912203 Functional Loss SNV dbSNP153 33..33 33 - - - 91621 RMVar_ID_91621 Human_SNP_ID_489610490 m1A Human chr12 + 6939040 6939040 6939040 GTCCTATGCTGAGCGGCTGGCAGCTGAGAGGCAGCACGCAGAAAGGGTGGCGGCCCTGGGCAATG GTCCTATGCTGAGCGGCTGGCAGCTGAGAGGCGGCACGCAGAAAGGGTGGCGGCCCTGGGCAATG A G ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6938990..6939179 26863196 MeRIP-seq:(Medium) rs1198816815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18975350,Human_RBP_ID_23573110 RMVar_hsa_circ_21092,RMVar_hsa_circ_64732 91622 RMVar_ID_91622 Human_SNP_ID_489611355 m1A Human chr12 - 6942126 6942126 6942126 GGGTGGCACACGATGCTACGCAAAACAGCCACATCTAACAGATGAAATAATCACACCAACGGGGC GGGTGGCACACGATGCTACGCAAAACAGCCACGTCTAACAGATGAAATAATCACACCAACGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6942076..6942272 26863196 MeRIP-seq:(Medium) rs1336152036 Functional Loss SNV dbSNP153 33..33 33 - - - 91623 RMVar_ID_91623 Human_SNP_ID_489612729 m1A Human chr12 + 6944170 6944170 6944170 CCCAACCGGCGGCCTTGAGCGCTGAGCAAGCAAAGGGTGAGAATCGTCCTAGTCAAGGCATAGGC CCCAACCGGCGGCCTTGAGCGCTGAGCAAGCAGAGGGTGAGAATCGTCCTAGTCAAGGCATAGGC A G C12orf57 Ensembl:ENSG00000111678 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6944160..6944238 26863196 MeRIP-seq:(Medium) rs1555145851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228805,Human_RBP_ID_12024511 Human_Splice_Rec_1333196,Human_Splice_Rec_1333197,Human_Splice_Rec_1333201,Human_Splice_Rec_1333203,Human_Splice_Rec_1333207,Human_Splice_Rec_1333211 RMVar_hsa_circ_122210,RMVar_hsa_circ_154662 91624 RMVar_ID_91624 Human_SNP_ID_489612983 m1A Human chr12 - 6944546 6944546 6944546 TGCAGCATCTTACCCATGTCGTTGCAGGCGTTATCCCGAGCCTCGTCCATGCGCACTGCATTCTC TGCAGCATCTTACCCATGTCGTTGCAGGCGTTTTCCCGAGCCTCGTCCATGCGCACTGCATTCTC T A U47924.2 Ensembl:ENSG00000272173 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6944495..6944695 26863196 MeRIP-seq:(Medium) rs962899716 Functional Loss SNV dbSNP153 33..33 33 - - - 91625 RMVar_ID_91625 Human_SNP_ID_489612989 m1A Human chr12 + 6944562 6944562 6944562 TGGACGAGGCTCGGGATAACGCCTGCAACGACATGGGTAAGATGCTGCAATTCGTGCTGCCCGTG TGGACGAGGCTCGGGATAACGCCTGCAACGACGTGGGTAAGATGCTGCAATTCGTGCTGCCCGTG A G C12orf57 Ensembl:ENSG00000111678 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6944526..6944600 26863196 MeRIP-seq:(Medium) rs920378510 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1168241,Human_RBP_ID_1477211,Human_RBP_ID_1800822 Human_Splice_Rec_1333190,Human_Splice_Rec_1333192,Human_Splice_Rec_1333193,Human_Splice_Rec_1333198,Human_Splice_Rec_1333199,Human_Splice_Rec_1333202,Human_Splice_Rec_1333204,Human_Splice_Rec_1333205,Human_Splice_Rec_1333208,Human_Splice_Rec_1333209,Human_Splice_Rec_1333213 Human_miRNA_ID_40713,Human_miRNA_ID_69437,Human_miRNA_ID_1937587,Human_miRNA_ID_1948687 RMVar_hsa_circ_105514,RMVar_hsa_circ_122210,RMVar_hsa_circ_154662,RMVar_hsa_circ_154663 91626 RMVar_ID_91626 Human_SNP_ID_489612990 m1A Human chr12 + 6944562 6944562 6944562 TGGACGAGGCTCGGGATAACGCCTGCAACGACATGGGTAAGATGCTGCAATTCGTGCTGCCCGTG TGGACGAGGCTCGGGATAACGCCTGCAACGACTTGGGTAAGATGCTGCAATTCGTGCTGCCCGTG A T C12orf57 Ensembl:ENSG00000111678 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6944526..6944600 26863196 MeRIP-seq:(Medium) rs920378510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1168241,Human_RBP_ID_1477211,Human_RBP_ID_1800822 Human_Splice_Rec_1333190,Human_Splice_Rec_1333192,Human_Splice_Rec_1333193,Human_Splice_Rec_1333198,Human_Splice_Rec_1333199,Human_Splice_Rec_1333202,Human_Splice_Rec_1333204,Human_Splice_Rec_1333205,Human_Splice_Rec_1333208,Human_Splice_Rec_1333209,Human_Splice_Rec_1333213 Human_miRNA_ID_40713,Human_miRNA_ID_69437,Human_miRNA_ID_1937587,Human_miRNA_ID_1948687 RMVar_hsa_circ_105514,RMVar_hsa_circ_122210,RMVar_hsa_circ_154662,RMVar_hsa_circ_154663 91627 RMVar_ID_91627 Human_SNP_ID_489613402 m1A Human chr12 + 6945742 6945742 6945742 CCAGGTGTCTTAGGCACGCTGGTCCTTAGGAGAAGGGTTGACCTTCCACTCCCTCTTGCAGGTGT CCAGGTGTCTTAGGCACGCTGGTCCTTAGGAGGAGGGTTGACCTTCCACTCCCTCTTGCAGGTGT A G C12orf57 Ensembl:ENSG00000111678 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6945741..6945877 26863196 MeRIP-seq:(Medium) rs781886883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105514,RMVar_hsa_circ_122210,RMVar_hsa_circ_154662,RMVar_hsa_circ_154663 91628 RMVar_ID_91628 Human_SNP_ID_489613435 m1A Human chr12 + 6945798 6945798 6945798 TGCAGGTGTCCTTAAGTTTGCTCGCTTGGTCAAGTCCTACGAAGCCCAGGATCCTGAGATCGCCA TGCAGGTGTCCTTAAGTTTGCTCGCTTGGTCAGGTCCTACGAAGCCCAGGATCCTGAGATCGCCA A G C12orf57 Ensembl:ENSG00000111678 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6945776..6945800 32194978 MeRIP-seq:(Medium) rs139068225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427429,Human_RBP_ID_1477214,Human_RBP_ID_3413399,Human_RBP_ID_4240526,Human_RBP_ID_8383129,Human_RBP_ID_9020805,Human_RBP_ID_17650049,Human_RBP_ID_17830211,Human_RBP_ID_22436237,Human_RBP_ID_23573131 Human_Splice_Rec_1333194,Human_Splice_Rec_1333200,Human_Splice_Rec_1333206,Human_Splice_Rec_1333210,Human_Splice_Rec_1333214 Human_miRNA_ID_2040256,Human_miRNA_ID_2554131,Human_miRNA_ID_3019237 Clinvar_Rec_522 GWAS_ID_11858 RMVar_hsa_circ_105514,RMVar_hsa_circ_122210,RMVar_hsa_circ_154662,RMVar_hsa_circ_86749,RMVar_hsa_circ_154663,RMVar_hsa_circ_154664 91629 RMVar_ID_91629 Human_SNP_ID_489613464 m1A Human chr12 + 6945872 6945872 6945872 GCAAGCTGAAGGCGCTGTTTCTGCCGCCCATGACCCTGCCACCCCATGGGCCTGCTGCTGGTGGC GCAAGCTGAAGGCGCTGTTTCTGCCGCCCATGGCCCTGCCACCCCATGGGCCTGCTGCTGGTGGC A G C12orf57 Ensembl:ENSG00000111678 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6945824..6945930 26863196 MeRIP-seq:(Medium) rs782398850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427432,Human_RBP_ID_17649971,Human_RBP_ID_22435780,Human_RBP_ID_26805445 RMVar_hsa_circ_105514,RMVar_hsa_circ_122210,RMVar_hsa_circ_154662,RMVar_hsa_circ_86749,RMVar_hsa_circ_154663,RMVar_hsa_circ_154664 91630 RMVar_ID_91630 Human_SNP_ID_489614357 m1A Human chr12 + 6948492 6948489 6948493 GGAAAGAAGGAAGGGAAGGAAGAAAGAAAAAGAGAAAGAAGGAAAAAAAGGAAAGAGCGAGAAAG GGAAAGAAGGAAGGGAAGGAAGAAAGAAAA____AAAGAAGGAAAAAAAGGAAAGAGCGAGAAAG AAGAG A PTPN6 Ensembl:ENSG00000111679 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6948454..6948629 26863196 MeRIP-seq:(Medium) rs1395103640 Functional Loss DEL dbSNP153 31..34 33 - - - 91631 RMVar_ID_91631 Human_SNP_ID_489614358 m1A Human chr12 + 6948492 6948489 6948493 GGAAAGAAGGAAGGGAAGGAAGAAAGAAAAAGAGAAAGAAGGAAAAAAAGGAAAGAGCGAGAAAG GGAAAGAAGGAAGGGAAGGAAGAAAGAAAAAG__AAAGAAGGAAAAAAAGGAAAGAGCGAGAAAG AAGAG AAG PTPN6 Ensembl:ENSG00000111679 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6948454..6948629 26863196 MeRIP-seq:(Medium) rs1395103640 Functional Loss DEL dbSNP153 33..34 33 - - - 91632 RMVar_ID_91632 Human_SNP_ID_489619815 m1A Human chr12 + 6966404 6966404 6966404 ACTCAGGTCCCACGTTCTTGGTGATACCCCACAGTGTGGCCACATCTCTCACCTGGTGAAACTTT ACTCAGGTCCCACGTTCTTGGTGATACCCCACTGTGTGGCCACATCTCTCACCTGGTGAAACTTT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6966401..6966450 26863196 MeRIP-seq:(Medium) rs782256465 Functional Loss SNV dbSNP153 33..33 33 - - - 91633 RMVar_ID_91633 Human_SNP_ID_489619820 m1A Human chr12 - 6966434 6966434 6966434 CTGACAACCTTGTGCTGAACCTACAGGATGAAAGTTTCACCAGGTGAGAGATGTGGCCACACTGT CTGACAACCTTGTGCTGAACCTACAGGATGAAGGTTTCACCAGGTGAGAGATGTGGCCACACTGT T C PHB2 Ensembl:ENSG00000215021 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6965526..6967299 32194978 MeRIP-seq:(Medium) rs1168231969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427497,Human_RBP_ID_1801133,Human_RBP_ID_17241422,Human_RBP_ID_17474692,Human_RBP_ID_17826349,Human_RBP_ID_18263863,Human_RBP_ID_18975351,Human_RBP_ID_22493974,Human_RBP_ID_25001695,Human_RBP_ID_26805449,Human_RBP_ID_26911486 Human_Splice_Rec_1333466,Human_Splice_Rec_1333467,Human_Splice_Rec_1333482,Human_Splice_Rec_1333483,Human_Splice_Rec_1333496,Human_Splice_Rec_1333497,Human_Splice_Rec_1333504,Human_Splice_Rec_1333505,Human_Splice_Rec_1333518,Human_Splice_Rec_1333542,Human_Splice_Rec_1333543,Human_Splice_Rec_1333550 RMVar_hsa_circ_121658,RMVar_hsa_circ_125056,RMVar_hsa_circ_112548,RMVar_hsa_circ_116151,RMVar_hsa_circ_110123,RMVar_hsa_circ_154674,RMVar_hsa_circ_154678,RMVar_hsa_circ_89625,RMVar_hsa_circ_93446,RMVar_hsa_circ_87254,RMVar_hsa_circ_154679,RMVar_hsa_circ_154676,RMVar_hsa_circ_154677,RMVar_hsa_circ_154675,RMVar_hsa_circ_154672,RMVar_hsa_circ_154673,RMVar_hsa_circ_154680,RMVar_hsa_circ_374995 91634 RMVar_ID_91634 Human_SNP_ID_489619836 m1A Human chr12 - 6966487 6966487 6966487 CTTATTTCCTGCCCTGTAGATCGCCACATCACAGAATCGTATCTATCTCACAGCTGACAACCTTG CTTATTTCCTGCCCTGTAGATCGCCACATCACGGAATCGTATCTATCTCACAGCTGACAACCTTG T C PHB2 Ensembl:ENSG00000215021 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:6966382..6966547;chr12:6966401..6966525 26863196 MeRIP-seq:(Medium) rs916439073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36163,Human_RBP_ID_1477499,Human_RBP_ID_12027654,Human_RBP_ID_17241422,Human_RBP_ID_17474692,Human_RBP_ID_17826351,Human_RBP_ID_18633123,Human_RBP_ID_25001697,Human_RBP_ID_26321191,Human_RBP_ID_26805450 Human_Splice_Rec_1333466,Human_Splice_Rec_1333467,Human_Splice_Rec_1333482,Human_Splice_Rec_1333483,Human_Splice_Rec_1333496,Human_Splice_Rec_1333497,Human_Splice_Rec_1333504,Human_Splice_Rec_1333505,Human_Splice_Rec_1333518,Human_Splice_Rec_1333542,Human_Splice_Rec_1333543,Human_Splice_Rec_1333550 Human_miRNA_ID_1345212,Human_miRNA_ID_2672785 RMVar_hsa_circ_121658,RMVar_hsa_circ_125056,RMVar_hsa_circ_112548,RMVar_hsa_circ_116151,RMVar_hsa_circ_110123,RMVar_hsa_circ_154674,RMVar_hsa_circ_154678,RMVar_hsa_circ_89625,RMVar_hsa_circ_93446,RMVar_hsa_circ_87254,RMVar_hsa_circ_154679,RMVar_hsa_circ_154676,RMVar_hsa_circ_154677,RMVar_hsa_circ_154675,RMVar_hsa_circ_154672,RMVar_hsa_circ_154673,RMVar_hsa_circ_154680,RMVar_hsa_circ_374995 91635 RMVar_ID_91635 Human_SNP_ID_489620147 m1A Human chr12 + 6967467 6967467 6967467 GCACCAGAAATGAAGGCAAGGCCACCAATGCTATTGATCTGGCCTTACAGTGGGGAGTCATGGCT GCACCAGAAATGAAGGCAAGGCCACCAATGCTTTTGATCTGGCCTTACAGTGGGGAGTCATGGCT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6967451..6967475 26863196 MeRIP-seq:(Medium) rs369576243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154682,RMVar_hsa_circ_154683 91636 RMVar_ID_91636 Human_SNP_ID_489621141 m1A Human chr12 - 6970276 6970276 6970276 GGCCTGATCACCACCCATCTCCCCACAGTGGAAGGCGGGCACAGAGCCATCTTCTTCAATCGGAT GGCCTGATCACCACCCATCTCCCCACAGTGGAGGGCGGGCACAGAGCCATCTTCTTCAATCGGAT T C PHB2 Ensembl:ENSG00000215021 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:6970226..6970300 26863196 MeRIP-seq:(Medium) rs1555151831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1477536,Human_RBP_ID_4247265,Human_RBP_ID_27425032 Human_Splice_Rec_1333472,Human_Splice_Rec_1333473,Human_Splice_Rec_1333488,Human_Splice_Rec_1333489,Human_Splice_Rec_1333502,Human_Splice_Rec_1333503,Human_Splice_Rec_1333508,Human_Splice_Rec_1333509,Human_Splice_Rec_1333520,Human_Splice_Rec_1333521,Human_Splice_Rec_1333532,Human_Splice_Rec_1333533,Human_Splice_Rec_1333552,Human_Splice_Rec_1333553,Human_Splice_Rec_1333564,Human_Splice_Rec_1333565,Human_Splice_Rec_1333570,Human_Splice_Rec_1333571,Human_Splice_Rec_1333576,Human_Splice_Rec_1333577,Human_Splice_Rec_1333583,Human_Splice_Rec_1333588 RMVar_hsa_circ_121658,RMVar_hsa_circ_112548,RMVar_hsa_circ_154678,RMVar_hsa_circ_154679 91637 RMVar_ID_91637 Human_SNP_ID_489621204 m1A Human chr12 + 6970406 6970406 6970406 GGAGGGACTGGAAGCGTCCGGCGAGCAGGCGGAGGTTGCTCACCGGTGAACACAGATTCGCGCAC GGAGGGACTGGAAGCGTCCGGCGAGCAGGCGGCGGTTGCTCACCGGTGAACACAGATTCGCGCAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6970401..6970525 32194978 MeRIP-seq:(Medium) rs782261697 Functional Loss SNV dbSNP153 33..33 33 - - - 91638 RMVar_ID_91638 Human_SNP_ID_489621205 m1A Human chr12 + 6970406 6970406 6970406 GGAGGGACTGGAAGCGTCCGGCGAGCAGGCGGAGGTTGCTCACCGGTGAACACAGATTCGCGCAC GGAGGGACTGGAAGCGTCCGGCGAGCAGGCGGTGGTTGCTCACCGGTGAACACAGATTCGCGCAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6970401..6970525 32194978 MeRIP-seq:(Medium) rs782261697 Functional Loss SNV dbSNP153 33..33 33 - - - 91639 RMVar_ID_91639 Human_SNP_ID_489621307 m1A Human chr12 + 6970624 6970624 6970624 CCGCCTCTACCCCGCTCCGGCTTAGGTACTGCACCCTTCACACGAGGGTTCGGGCCCGTAAGGCT CCGCCTCTACCCCGCTCCGGCTTAGGTACTGCCCCCTTCACACGAGGGTTCGGGCCCGTAAGGCT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:6970576..6970675;chr12:6970381..6970725;chr12:6970477..6970700 26863196 MeRIP-seq:(Medium) rs1262677667 Functional Loss SNV dbSNP153 33..33 33 - - - 91640 RMVar_ID_91640 Human_SNP_ID_489621309 m1A Human chr12 + 6970633 6970633 6970633 CCCCGCTCCGGCTTAGGTACTGCACCCTTCACACGAGGGTTCGGGCCCGTAAGGCTGGCGAAAGA CCCCGCTCCGGCTTAGGTACTGCACCCTTCACCCGAGGGTTCGGGCCCGTAAGGCTGGCGAAAGA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:6970544..6970650 26863410 MeRIP-seq:(Medium) rs1486672959 Functional Loss SNV dbSNP153 33..33 33 - - - 91641 RMVar_ID_91641 Human_SNP_ID_489621466 m1A Human chr12 + 6970976 6970976 6970976 ATTCAAGCCTCGTGAACGAAGCGGTGGGGAGCAGGCACAGGACTGGGATGCTCTGCCACCCAAGC ATTCAAGCCTCGTGAACGAAGCGGTGGGGAGCGGGCACAGGACTGGGATGCTCTGCCACCCAAGC A G EMG1 Ensembl:ENSG00000126749 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr12:6970920..6971141;chr12:6970920..6971137;chr12:6970920..6974547;chr12:6970892..6974375;chr12:6970926..6971100 26863196 MeRIP-seq:(Medium) rs1402722258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4240723,Human_RBP_ID_9364642,Human_RBP_ID_12027773,Human_RBP_ID_22910716 91642 RMVar_ID_91642 Human_SNP_ID_489622440 m1A Human chr12 - 6974309 6974309 6974309 TACCTGAAGAACAGGGAACATGACGAGAGAACAGCATAAGCTTCTGTTACCTAGCCCCGTGGTTC TACCTGAAGAACAGGGAACATGACGAGAGAACGGCATAAGCTTCTGTTACCTAGCCCCGTGGTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6974307..6974420 26863196 MeRIP-seq:(Medium) rs782509014 Functional Loss SNV dbSNP153 33..33 33 - - - 91643 RMVar_ID_91643 Human_SNP_ID_489622471 m1A Human chr12 - 6974387 6974387 6974387 CGCTTCCCCAGGGTCCCGTCCATTCTTCAACAATATAGACTTGTGCTTGTCACAGTTGAGTAGCT CGCTTCCCCAGGGTCCCGTCCATTCTTCAACAGTATAGACTTGTGCTTGTCACAGTTGAGTAGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6971019..6974416 32194978 MeRIP-seq:(Medium) rs782689019 Functional Loss SNV dbSNP153 33..33 33 - - - 91644 RMVar_ID_91644 Human_SNP_ID_489632806 m1A Human chr12 + 7018418 7018418 7018418 CACCACAGTCCCCTCGTCCCCCTCCGCTGAGGACGCCATCTTAACTCCGGGAGCCCCACAGGGAC CACCACAGTCCCCTCGTCCCCCTCCGCTGAGGGCGCCATCTTAACTCCGGGAGCCCCACAGGGAC A G C1S Ensembl:ENSG00000182326 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6983436..7018465 26863196 MeRIP-seq:(Medium) rs1555157805 Functional Loss SNV dbSNP153 33..33 33 - - - 91645 RMVar_ID_91645 Human_SNP_ID_489643510 m1A Human chr12 - 7060798 7060798 7060798 AGTGGGCATGCTGGGCAACCCCTCTGGCCCCCAGGGACAGCAGCACAGGGCCTTGACGCTCCCTC AGTGGGCATGCTGGGCAACCCCTCTGGCCCCCCGGGACAGCAGCACAGGGCCTTGACGCTCCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:7060750..7060892 26863196 MeRIP-seq:(Medium) rs986730916 Functional Loss SNV dbSNP153 33..33 33 - - - 91646 RMVar_ID_91646 Human_SNP_ID_489648997 m1A Human chr12 - 7081252 7081252 7081252 AACCCCGTGGAACAGAGGCAGCGCATCATCGGAGGGCAAAAAGCCAAGATGGGCAACTTCCCCTG AACCCCGTGGAACAGAGGCAGCGCATCATCGGCGGGCAAAAAGCCAAGATGGGCAACTTCCCCTG T G C1R Ensembl:ENSG00000159403 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7081203..7085887 32194978 MeRIP-seq:(Medium) rs767614022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1333978,Human_Splice_Rec_1333998,Human_Splice_Rec_1334004,Human_Splice_Rec_1334024,Human_Splice_Rec_1334044,Human_Splice_Rec_1334052,Human_Splice_Rec_1334070 91647 RMVar_ID_91647 Human_SNP_ID_489650761 m1A Human chr12 + 7088912 7088912 7088912 GACTCATCTGTGAAGAACAGCAGATCCACAGCATTGCTGCTGGTGTCGAGGTCGGGGGGCCTTTG GACTCATCTGTGAAGAACAGCAGATCCACAGCGTTGCTGCTGGTGTCGAGGTCGGGGGGCCTTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7088861..7088961 32194978 MeRIP-seq:(Medium) rs1228618331 Functional Loss SNV dbSNP153 33..33 33 - - - 91648 RMVar_ID_91648 Human_SNP_ID_489651893 m1A Human chr12 - 7092402 7092402 7092402 GAAGACGCTGTCGGGAGAGCCCAGGATTCAACACGGGCCTTGAGAAATGTGAGTAAGGGTGATGG GAAGACGCTGTCGGGAGAGCCCAGGATTCAACGCGGGCCTTGAGAAATGTGAGTAAGGGTGATGG T C C1RL,C1R Ensembl:ENSG00000139178,Ensembl:ENSG00000159403 Protein coding,Protein coding 3'UTR,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:7091607..7092506 26863196 MeRIP-seq:(Medium) rs1327445757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1333979,Human_Splice_Rec_1334025,Human_Splice_Rec_1334071,Human_Splice_Rec_1334079,Human_Splice_Rec_1334085,Human_Splice_Rec_1334091,Human_Splice_Rec_1334099,Human_Splice_Rec_1334111,Human_Splice_Rec_1334115,Human_Splice_Rec_1334122,Human_Splice_Rec_1334123 91649 RMVar_ID_91649 Human_SNP_ID_489654183 m1A Human chr12 + 7101028 7101028 7101028 AGAGCCAGAGATCAGAGGAAGACTTACTTTTTAGCATACTTAAAAAAATGATATTTTATCATGTG AGAGCCAGAGATCAGAGGAAGACTTACTTTTTGGCATACTTAAAAAAATGATATTTTATCATGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:7100990..7101078 26863196 MeRIP-seq:(Medium) rs1374882398 Functional Loss SNV dbSNP153 33..33 33 - - - 91650 RMVar_ID_91650 Human_SNP_ID_489654333 m1A Human chr12 - 7101286 7101278 7101286 AGCCTGGGAGACACGGAGAAACTAGAAGAGAGAAAGAGAGGAAGAGAGGAAGGAAGGAAGGAGGA AGCCTGGGAGACACGGAGAAACTAGAAGAGAG________GAAGAGAGGAAGGAAGGAAGGAGGA CCTCTCTTT C C1RL Ensembl:ENSG00000139178 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:7101284..7101368 26863196 MeRIP-seq:(Medium) rs1395323266 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_811657 RMVar_hsa_circ_154704,RMVar_hsa_circ_284512,RMVar_hsa_circ_83503 91651 RMVar_ID_91651 Human_SNP_ID_489658270 m1A Human chr12 + 7118576 7118576 7118576 TTCTATAGAACAGAGGATGGAGAGGCCACACGACAATAGGCACACGCACCGTACATTGAAGAAGT TTCTATAGAACAGAGGATGGAGAGGCCACACGGCAATAGGCACACGCACCGTACATTGAAGAAGT A G C1RL-AS1 Ensembl:ENSG00000205885 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:7118525..7118657 26863196 MeRIP-seq:(Medium) rs749223162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5560694 RMVar_hsa_circ_25983,RMVar_hsa_circ_59356 91652 RMVar_ID_91652 Human_SNP_ID_489658357 m1A Human chr12 + 7118938 7118938 7118938 AGAAGAAGAGGAGGAGGAGGAGGAGGAAGAAGAAAGATGGTGAGATATCCTGCAGGAGACCAGGG AGAAGAAGAGGAGGAGGAGGAGGAGGAAGAAGGAAGATGGTGAGATATCCTGCAGGAGACCAGGG A G C1RL-AS1 Ensembl:ENSG00000205885 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:7118901..7119010 26863196 MeRIP-seq:(Medium) rs1365676216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874256,Human_RBP_ID_1479766,Human_RBP_ID_18976807 Human_Splice_Rec_1334210,Human_Splice_Rec_1334211,Human_Splice_Rec_1334228,Human_Splice_Rec_1334229 RMVar_hsa_circ_25983,RMVar_hsa_circ_59356 91653 RMVar_ID_91653 Human_SNP_ID_489660772 m1A Human chr12 + 7128774 7128774 7128774 CAAAGCGGTAGTAGCCAGTGAGGTTGGGAGGCATTGTGTGGATGAAGGTTTCAGGAGAATGCAGG CAAAGCGGTAGTAGCCAGTGAGGTTGGGAGGCGTTGTGTGGATGAAGGTTTCAGGAGAATGCAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:7128723..7128901 26863196 MeRIP-seq:(Medium) rs375075718 Functional Loss SNV dbSNP153 33..33 33 - - - 91654 RMVar_ID_91654 Human_SNP_ID_489668057 m1A Human chr12 + 7155929 7155929 7155929 TGCGTGGCAGCTGAGTGTGCTGGCTGCTGGGGAGAGGGGCGCTGCAGCAGGGTGTGGGTGTGAGT TGCGTGGCAGCTGAGTGTGCTGGCTGCTGGGGCGAGGGGCGCTGCAGCAGGGTGTGGGTGTGAGT A C CLSTN3 Ensembl:ENSG00000139182 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:7155903..7156029 26863196 MeRIP-seq:(Medium) rs1379359140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21966993 RMVar_hsa_circ_121312,RMVar_hsa_circ_154710 91655 RMVar_ID_91655 Human_SNP_ID_489676028 m1A Human chr12 + 7189884 7189884 7189884 GGGCCGGGGAGATGGGCGGTGGGGAGCGCGGGAGGGACCGGGCCGAGCCGGGGGAAGGGCTCCGG GGGCCGGGGAGATGGGCGGTGGGGAGCGCGGGGGGGACCGGGCCGAGCCGGGGGAAGGGCTCCGG A G PEX5 Ensembl:ENSG00000139197 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:7189729..7190536 26863196 MeRIP-seq:(Medium) rs1034943468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4245996,Human_RBP_ID_5348145,Human_RBP_ID_8177333,Human_RBP_ID_18934305,Human_RBP_ID_19055906,Human_RBP_ID_26777247 Human_Splice_Rec_1334605 91656 RMVar_ID_91656 Human_SNP_ID_489676104 m1A Human chr12 + 7190046 7190046 7190046 TCGGGCAGTGTCGCCGTCCAGCCTGGTTGTTGAAGCGTCCCCGTGGTCCCCCGGGGTCCAGGCCC TCGGGCAGTGTCGCCGTCCAGCCTGGTTGTTGGAGCGTCCCCGTGGTCCCCCGGGGTCCAGGCCC A G PEX5 Ensembl:ENSG00000139197 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7190036..7190286 32194978 MeRIP-seq:(Medium) rs1348037796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247279,Human_RBP_ID_19060934,Human_RBP_ID_22177553 Human_Splice_Rec_1334436,Human_Splice_Rec_1334554 91657 RMVar_ID_91657 Human_SNP_ID_489676135 m1A Human chr12 - 7190150 7190150 7190150 TCCTGCCGCCCCCCTCAAAGGCCACCGCTTCCAGCCTGCGCCTCTGCAGAGGCCTCCGCGACTAC TCCTGCCGCCCCCCTCAAAGGCCACCGCTTCCTGCCTGCGCCTCTGCAGAGGCCTCCGCGACTAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:7190140..7190524 26863196 MeRIP-seq:(Medium) rs1010715741 Functional Loss SNV dbSNP153 33..33 33 - - - 91658 RMVar_ID_91658 Human_SNP_ID_489676215 m1A Human chr12 + 7190384 7190384 7190384 TGTCCATCAGAGAGCTGGCGGTCACCATGGCAATGCGGGAGCTGGTGGAGGCCGAATGCGGGGGT TGTCCATCAGAGAGCTGGCGGTCACCATGGCAGTGCGGGAGCTGGTGGAGGCCGAATGCGGGGGT A G PEX5 Ensembl:ENSG00000139197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:7189727..7190504 26863196 MeRIP-seq:(Medium) rs752899987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427985,Human_RBP_ID_4247281,Human_RBP_ID_5348146,Human_RBP_ID_8785355 Human_Splice_Rec_1334422,Human_Splice_Rec_1334438,Human_Splice_Rec_1334470,Human_Splice_Rec_1334476,Human_Splice_Rec_1334524,Human_Splice_Rec_1334556,Human_Splice_Rec_1334562,Human_Splice_Rec_1334576,Human_Splice_Rec_1334606,Human_Splice_Rec_1334636,Human_Splice_Rec_1334658 RMVar_hsa_circ_154713,RMVar_hsa_circ_348665,RMVar_hsa_circ_376073,RMVar_hsa_circ_154714 91659 RMVar_ID_91659 Human_SNP_ID_489676216 m1A Human chr12 + 7190384 7190384 7190384 TGTCCATCAGAGAGCTGGCGGTCACCATGGCAATGCGGGAGCTGGTGGAGGCCGAATGCGGGGGT TGTCCATCAGAGAGCTGGCGGTCACCATGGCATTGCGGGAGCTGGTGGAGGCCGAATGCGGGGGT A T PEX5 Ensembl:ENSG00000139197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:7189727..7190504 26863196 MeRIP-seq:(Medium) rs752899987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427985,Human_RBP_ID_4247281,Human_RBP_ID_5348146,Human_RBP_ID_8785355 Human_Splice_Rec_1334422,Human_Splice_Rec_1334438,Human_Splice_Rec_1334470,Human_Splice_Rec_1334476,Human_Splice_Rec_1334524,Human_Splice_Rec_1334556,Human_Splice_Rec_1334562,Human_Splice_Rec_1334576,Human_Splice_Rec_1334606,Human_Splice_Rec_1334636,Human_Splice_Rec_1334658 RMVar_hsa_circ_154713,RMVar_hsa_circ_348665,RMVar_hsa_circ_376073,RMVar_hsa_circ_154714 91660 RMVar_ID_91660 Human_SNP_ID_489676239 m1A Human chr12 - 7190436 7190433 7190437 GAAGGGCCTTGTCCTGGGTGAAGTGCCCGGCGAGCTTCATGAGCGGGTTGGCACCCCCGCATTCG GAAGGGCCTTGTCCTGGGTGAAGTGCCCGGC____TTCATGAGCGGGTTGGCACCCCCGCATTCG AGCTC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7190385..7190585 32194978 MeRIP-seq:(Medium) rs1261001030 Functional Loss DEL dbSNP153 32..35 33 - - - 91661 RMVar_ID_91661 Human_SNP_ID_489682488 m1A Human chr12 - 7208583 7208583 7208583 GCCCCTTCTTCAGCAGGTGTCACCAGATGGGCATAGGCTGGTGTGTACCGCAGCCAGTCTCGTAG GCCCCTTCTTCAGCAGGTGTCACCAGATGGGCGTAGGCTGGTGTGTACCGCAGCCAGTCTCGTAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7208532..7209068 32194978 MeRIP-seq:(Medium) rs553222410 Functional Loss SNV dbSNP153 33..33 33 - - - 91662 RMVar_ID_91662 Human_SNP_ID_489902359 m1A Human chr12 + 8047990 8047951 8047990 TCAACAGCAGCAGCAGCAGCAGCAGCCGCCACAGCCACCTCCCCAGCAGTCCCAGCCACAGCAGC _________________________________GCCACCTCCCCAGCAGTCCCAGCCACAGCAGC CGCCACCTCAACAGCAGCAGCAGCAGCAGCAGCCGCCACA C FOXJ2 Ensembl:ENSG00000065970 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:8047939..8048027 26863196 MeRIP-seq:(Medium) rs748200100 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_17357525 Human_miRNA_ID_841981,Human_miRNA_ID_2367346,Human_miRNA_ID_2684876,Human_miRNA_ID_3015143 RMVar_hsa_circ_95592,RMVar_hsa_circ_154739,RMVar_hsa_circ_367953 91663 RMVar_ID_91663 Human_SNP_ID_489902384 m1A Human chr12 + 8047990 8047990 8047990 TCAACAGCAGCAGCAGCAGCAGCAGCCGCCACAGCCACCTCCCCAGCAGTCCCAGCCACAGCAGC TCAACAGCAGCAGCAGCAGCAGCAGCCGCCACCGCCACCTCCCCAGCAGTCCCAGCCACAGCAGC A C FOXJ2 Ensembl:ENSG00000065970 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:8047939..8048027 26863196 MeRIP-seq:(Medium) rs1201517066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357525 Human_miRNA_ID_841981,Human_miRNA_ID_2367346,Human_miRNA_ID_2684876,Human_miRNA_ID_3015143 RMVar_hsa_circ_95592,RMVar_hsa_circ_154739,RMVar_hsa_circ_367953 91664 RMVar_ID_91664 Human_SNP_ID_489953772 m1A Human chr12 - 8242873 8242834 8242874 AGGGTTTCGATCGCCGCTTCCTGGCGGCGCGCACACTGCGCTCCTTCCCCTGGCATGTGGGCGGC AGGGTTTCGATCGCCGCTTCCTGGCGGCGCG__________________________________ TCGCCCCGCCGCCCACATGCCAGGGGAAGGAGCGCAGTGTG T FAM86FP Ensembl:ENSG00000164845 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:8242829..8242932 26863196 MeRIP-seq:(Medium) rs925244661 Functional Loss DEL dbSNP153 32..65 33 - - - Human_Splice_Rec_1336045 91665 RMVar_ID_91665 Human_SNP_ID_489953793 m1A Human chr12 - 8242873 8242873 8242873 AGGGTTTCGATCGCCGCTTCCTGGCGGCGCGCACACTGCGCTCCTTCCCCTGGCATGTGGGCGGC AGGGTTTCGATCGCCGCTTCCTGGCGGCGCGCTCACTGCGCTCCTTCCCCTGGCATGTGGGCGGC T A FAM86FP Ensembl:ENSG00000164845 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:8242829..8242932 26863196 MeRIP-seq:(Medium) rs1202657849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1336045 91666 RMVar_ID_91666 Human_SNP_ID_490001882 m1A Human chr12 - 8396719 8396719 8396719 CCGCGCCGCGCGGACCCACCGAGCCCGCGCTCAGACGCCCCAGCTCCGCCGAGAGGCCGCTTGCG CCGCGCCGCGCGGACCCACCGAGCCCGCGCTCCGACGCCCCAGCTCCGCCGAGAGGCCGCTTGCG T G LINC00937 Ensembl:ENSG00000226091 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:8396633..8396733 26863410 MeRIP-seq:(Medium) rs1303068550 Functional Loss SNV dbSNP153 33..33 33 - - - 91667 RMVar_ID_91667 Human_SNP_ID_490070602 m1A Human chr12 + 8681661 8681661 8681661 GGGCTGGAAATAAAGCTCTATAAAAACTCATGAACAGTGGGTCTTGATGAGCTTCCGGGTTTATG GGGCTGGAAATAAAGCTCTATAAAAACTCATGGACAGTGGGTCTTGATGAGCTTCCGGGTTTATG A G RIMKLB Ensembl:ENSG00000166532 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:8681639..8681740 26863196 MeRIP-seq:(Medium) rs755699837 Functional Loss SNV dbSNP153 33..33 33 - - - 91668 RMVar_ID_91668 Human_SNP_ID_490074818 m1A Human chr12 - 8698042 8698038 8698042 GCTTCTCCCTCACCCCACTCCCACACACTCTCACTCCCACACACTCACACCCGGCCGCTCCTCGT GCTTCTCCCTCACCCCACTCCCACACACTCTC____CCACACACTCACACCCGGCCGCTCCTCGT GGAGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:8697910..8699811 26863196 MeRIP-seq:(Medium) rs1266327374 Functional Loss DEL dbSNP153 33..36 33 - - - 91669 RMVar_ID_91669 Human_SNP_ID_490074827 m1A Human chr12 + 8698069 8698069 8698069 GGGAGTGAGAGTGTGTGGGAGTGGGGTGAGGGAGAAGCTGACGGGACGCGAGGCTGTGAGAAACT GGGAGTGAGAGTGTGTGGGAGTGGGGTGAGGGGGAAGCTGACGGGACGCGAGGCTGTGAGAAACT A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:8697908..8699811 26863196 MeRIP-seq:(Medium) rs1369889501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555765,Human_RBP_ID_5644928,Human_RBP_ID_23577449,Human_RBP_ID_26768356 RMVar_hsa_circ_98066,RMVar_hsa_circ_154751 91670 RMVar_ID_91670 Human_SNP_ID_490074863 m1A Human chr12 + 8698183 8698183 8698183 GGAGGAGAAAGGAGGCGGCTCCCGGTATCCCGACCCCCTCCCCCTCCTCTCCTTCCCCCACTTCC GGAGGAGAAAGGAGGCGGCTCCCGGTATCCCGCCCCCCTCCCCCTCCTCTCCTTCCCCCACTTCC A C RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:8697973..8698307 26863196 MeRIP-seq:(Medium) rs1236984638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942728,Human_RBP_ID_5438254,Human_RBP_ID_5492180,Human_RBP_ID_23577453 RMVar_hsa_circ_98066,RMVar_hsa_circ_154751 91671 RMVar_ID_91671 Human_SNP_ID_490134656 m1A Human chr12 + 8914330 8914321 8914330 GGTAAAAAAGAGGAGAAAGAGAGCAAGAGAGGAAAAAACCCCTGGGCCTGGAGCGCAGAGGCCCG GGTAAAAAAGAGGAGAAAGAGAGC_________AAAAACCCCTGGGCCTGGAGCGCAGAGGCCCG CAAGAGAGGA C PHC1 Ensembl:ENSG00000111752 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:8914303..8914402 26863196 MeRIP-seq:(Medium) rs1294116397 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_5170701 91672 RMVar_ID_91672 Human_SNP_ID_490134657 m1A Human chr12 + 8914322 8914322 8914322 AAGAAGGGGGTAAAAAAGAGGAGAAAGAGAGCAAGAGAGGAAAAAACCCCTGGGCCTGGAGCGCA AAGAAGGGGGTAAAAAAGAGGAGAAAGAGAGCGAGAGAGGAAAAAACCCCTGGGCCTGGAGCGCA A G PHC1 Ensembl:ENSG00000111752 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:8914272..8914402 26863196 MeRIP-seq:(Medium) rs1224030341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5170701 91673 RMVar_ID_91673 Human_SNP_ID_490134679 m1A Human chr12 + 8914403 8914403 8914403 GTCGCCATGGCAACGGGCGCCGGCAGGAAACGAGGGACGCGCGGGAGGGAGGGGGCGGAGGGCGC GTCGCCATGGCAACGGGCGCCGGCAGGAAACGGGGGACGCGCGGGAGGGAGGGGGCGGAGGGCGC A G PHC1 Ensembl:ENSG00000111752 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:8914245..8914414;chr12:8914267..8914428 26863196 MeRIP-seq:(Medium) rs775288333 Functional Loss SNV dbSNP153 33..33 33 - - - 91674 RMVar_ID_91674 Human_SNP_ID_490138063 m1A Human chr12 + 8927386 8927386 8927386 GGAGGGGAATGTGCAGTTCCTACATGGTGATGAGGGAGCCAGTGGAGAAGAAGTGGAAGAGGAGG GGAGGGGAATGTGCAGTTCCTACATGGTGATGCGGGAGCCAGTGGAGAAGAAGTGGAAGAGGAGG A C PHC1 Ensembl:ENSG00000111752 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:8927343..8927503 26863196 MeRIP-seq:(Medium) rs768345316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23578243 RMVar_hsa_circ_127909,RMVar_hsa_circ_92723,RMVar_hsa_circ_115923,RMVar_hsa_circ_113216,RMVar_hsa_circ_154779,RMVar_hsa_circ_122767,RMVar_hsa_circ_102274,RMVar_hsa_circ_154783,RMVar_hsa_circ_90682,RMVar_hsa_circ_154784,RMVar_hsa_circ_154781,RMVar_hsa_circ_154782,RMVar_hsa_circ_154780,RMVar_hsa_circ_84689,RMVar_hsa_circ_107611,RMVar_hsa_circ_117482,RMVar_hsa_circ_105830,RMVar_hsa_circ_154788,RMVar_hsa_circ_154790,RMVar_hsa_circ_154792,RMVar_hsa_circ_81061,RMVar_hsa_circ_154791,RMVar_hsa_circ_154789,RMVar_hsa_circ_154787 91675 RMVar_ID_91675 Human_SNP_ID_490143041 m1A Human chr12 - 8945513 8945513 8945513 CTACATCTTCAGGGTGTGCCGGGAAGCTGGCAACCACACTTCTGGGGCAGGCCTGGTGCAAATCA CTACATCTTCAGGGTGTGCCGGGAAGCTGGCAGCCACACTTCTGGGGCAGGCCTGGTGCAAATCA T C M6PR Ensembl:ENSG00000003056 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:8945401..8946372 32194978 MeRIP-seq:(Medium) rs751187988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36216,Human_RBP_ID_755318,Human_RBP_ID_1478613,Human_RBP_ID_17240988,Human_RBP_ID_17356514,Human_RBP_ID_17828619,Human_RBP_ID_18434848,Human_RBP_ID_22436281,Human_RBP_ID_22756591,Human_RBP_ID_22795519,Human_RBP_ID_25016711 Human_Splice_Rec_1336984,Human_Splice_Rec_1336985,Human_Splice_Rec_1337000,Human_Splice_Rec_1337001,Human_Splice_Rec_1337008,Human_Splice_Rec_1337009,Human_Splice_Rec_1337026,Human_Splice_Rec_1337027,Human_Splice_Rec_1337033,Human_Splice_Rec_1337040,Human_Splice_Rec_1337041,Human_Splice_Rec_1337046,Human_Splice_Rec_1337050,Human_Splice_Rec_1337052 RMVar_hsa_circ_267541 91676 RMVar_ID_91676 Human_SNP_ID_490148245 m1A Human chr12 + 8967934 8967932 8967935 GGAGAACCTAGAGCAATCATAACAGAAAGAAAAGAAGGAAGGAAGGGAGAAAAGAAAGAAAGAAA GGAGAACCTAGAGCAATCATAACAGAAAGAA___AAGGAAGGAAGGGAGAAAAGAAAGAAAGAAA AAAG A KLRG1 Ensembl:ENSG00000139187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:8967912..8967997 26863196 MeRIP-seq:(Medium) rs1421432700 Functional Loss DEL dbSNP153 32..34 33 - - - 91677 RMVar_ID_91677 Human_SNP_ID_490169302 m1A Human chr12 - 9064684 9064684 9064684 GGGGCCCCTCTCTGCCTGCCCCTCCGTGCCCGACTACACTGCTTCCCCTCCGGCGGGCGACTCAG GGGGCCCCTCTCTGCCTGCCCCTCCGTGCCCGCCTACACTGCTTCCCCTCCGGCGGGCGACTCAG T G LINC00612 Ensembl:ENSG00000214851 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:9064528..9064775 26863196 MeRIP-seq:(Medium) rs1235711209 Functional Loss SNV dbSNP153 33..33 33 - - - 91678 RMVar_ID_91678 Human_SNP_ID_490187676 m1A Human chr12 - 9145026 9145026 9145026 ACACATAGGCTGAAAGTGAAGGGATGAAAAAGATATCCCATGCAAATGGTAATCACAAGAGAGTA ACACATAGGCTGAAAGTGAAGGGATGAAAAAGTTATCCCATGCAAATGGTAATCACAAGAGAGTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:9144976..9145090;chr12:9144976..9145050 26863196 MeRIP-seq:(Medium) rs897957719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154815,RMVar_hsa_circ_154828 91679 RMVar_ID_91679 Human_SNP_ID_490209765 m1A Human chr12 + 9238345 9238344 9238345 CCAGTTAGAAAGCTATTGAGAGCCTGCAAGAGAAAGGACTAGAATAGTAGAGATGGAGAGAAGTG CCAGTTAGAAAGCTATTGAGAGCCTGCAAGAG_AAGGACTAGAATAGTAGAGATGGAGAGAAGTG GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:9238094..9238463 26863196 MeRIP-seq:(Medium) rs1355086404 Functional Loss DEL dbSNP153 33..33 33 - - - 91680 RMVar_ID_91680 Human_SNP_ID_490227566 m1A Human chr12 + 9310388 9310388 9310388 GACAACATCTGCCCCTTGTCATCTGCAGCGGGATCTCCAACCAGCCGCTGGAATTCACCTTCCAG GACAACATCTGCCCCTTGTCATCTGCAGCGGGGTCTCCAACCAGCCGCTGGAATTCACCTTCCAG A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12317441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875911,Human_RBP_ID_18527004 Human_Splice_Rec_1337593 RMVar_hsa_circ_44481,RMVar_hsa_circ_107891,RMVar_hsa_circ_154842 91681 RMVar_ID_91681 Human_SNP_ID_490227738 m1A Human chr12 + 9310928 9310928 9310928 CCCCCAGGGACGCTAGTGCTGTGACATGTGTCAGAAAGGCGCAGTCAGCAGCAGCGGCTGGGTGT CCCCCAGGGACGCTAGTGCTGTGACATGTGTCGGAAAGGCGCAGTCAGCAGCAGCGGCTGGGTGT A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs181270058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229540,Human_RBP_ID_8940878,Human_RBP_ID_17243528,Human_RBP_ID_23579024 RMVar_hsa_circ_107891,RMVar_hsa_circ_154842 91682 RMVar_ID_91682 Human_SNP_ID_490228256 m1A Human chr12 + 9312519 9312519 9312519 TCACCTGGACCCCTGCTGCTGGCATTGGCCACAAAGCCTCCTGGTCTGGCTCCAAAGCCTGGCAG TCACCTGGACCCCTGCTGCTGGCATTGGCCACGAAGCCTCCTGGTCTGGCTCCAAAGCCTGGCAG A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12831770 Functional Loss SNV dbSNP153 33..33 33 - - - 91683 RMVar_ID_91683 Human_SNP_ID_490260919 m1A Human chr12 - 9420275 9420275 9420275 GAGACCTGGCACCCTGAACCTGTCTCTGGGAAATGTCCTCTGTCTTTCTCAGATATTCCAGGAAC GAGACCTGGCACCCTGAACCTGTCTCTGGGAAGTGTCCTCTGTCTTTCTCAGATATTCCAGGAAC T C DDX12P Ensembl:ENSG00000214826 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10843741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1337689 RMVar_hsa_circ_115903,RMVar_hsa_circ_154844 91684 RMVar_ID_91684 Human_SNP_ID_490262758 m1A Human chr12 - 9425547 9425547 9425547 AGTCAGGCCAGCGTCCCGCAACCAGCTTCCCCACTGATGCACATCGAAGGCTTCCTGGCAGCTCT AGTCAGGCCAGCGTCCCGCAACCAGCTTCCCCGCTGATGCACATCGAAGGCTTCCTGGCAGCTCT T C DDX12P Ensembl:ENSG00000214826 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:9422583..9425569 32194978 MeRIP-seq:(Medium) rs116562190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875771,Human_RBP_ID_3942747,Human_RBP_ID_5093832,Human_RBP_ID_8247981,Human_RBP_ID_9364652,Human_RBP_ID_12063221,Human_RBP_ID_17358047,Human_RBP_ID_18527113,Human_RBP_ID_18635100,Human_RBP_ID_18975382,Human_RBP_ID_21959615,Human_RBP_ID_21968170 Human_Splice_Rec_1337680,Human_Splice_Rec_1337681 91685 RMVar_ID_91685 Human_SNP_ID_490266732 m1A Human chr12 - 9438022 9438022 9438022 TTGTGCAGAAGAAAGAAGAGAGGGACCTGGTGAACCGACTGAAGGTGAGACCTGGGGTATCCGGA TTGTGCAGAAGAAAGAAGAGAGGGACCTGGTGGACCGACTGAAGGTGAGACCTGGGGTATCCGGA T C DDX12P Ensembl:ENSG00000214826 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:9437442..9438064 32194978 MeRIP-seq:(Medium) rs1416988729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229591,Human_RBP_ID_810212,Human_RBP_ID_874295,Human_RBP_ID_3941472,Human_RBP_ID_5462299,Human_RBP_ID_5561030,Human_RBP_ID_8247987,Human_RBP_ID_8787649,Human_RBP_ID_9364655,Human_RBP_ID_17358052,Human_RBP_ID_17475162,Human_RBP_ID_17673044,Human_RBP_ID_18527119,Human_RBP_ID_18976854,Human_RBP_ID_19055948,Human_RBP_ID_21968101,Human_RBP_ID_22414727,Human_RBP_ID_22572164,Human_RBP_ID_22795584,Human_RBP_ID_24543251,Human_RBP_ID_24551206,Human_RBP_ID_27806452 Human_Splice_Rec_1337657 RMVar_hsa_circ_70905 91686 RMVar_ID_91686 Human_SNP_ID_490269427 m1A Human chr12 - 9448060 9448060 9448060 GCTGTGTGGCAGCAGAGGTCCTTAGGACGAGGAGCAGCGGGACGAGGAAGGGCAGACTGGTGAAA GCTGTGTGGCAGCAGAGGTCCTTAGGACGAGGTGCAGCGGGACGAGGAAGGGCAGACTGGTGAAA T A DDX12P Ensembl:ENSG00000214826 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:9447972..9448192;chr12:9447953..9448197 26863196 MeRIP-seq:(Medium) rs1349257242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5555792,Human_RBP_ID_8248045,Human_RBP_ID_12064062,Human_RBP_ID_26321205 91687 RMVar_ID_91687 Human_SNP_ID_645941349 m1A Human chr18 - 45063343 45063343 45063343 TGGGCTTCTGGCCTCTTTTGCTGGGCAGGTCGATGCATTTTTCCAGCACCGGCATTTGGTCTCTG TGGGCTTCTGGCCTCTTTTGCTGGGCAGGTCGCTGCATTTTTCCAGCACCGGCATTTGGTCTCTG T G HSALNG0121247 RNACentral:URS0000EB6F4A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:45063302..45063446 26863196 MeRIP-seq:(Medium) rs1308636141 Functional Loss SNV dbSNP153 33..33 33 - - - 91688 RMVar_ID_91688 Human_SNP_ID_646141519 m1A Human chr18 - 45850208 45850208 45850208 GCCGCACATCAAGACGGGAATCAAGCAAGACCAAGGCCCTGTGGACTGAGCAGCGTGGAGGGCGA GCCGCACATCAAGACGGGAATCAAGCAAGACCGAGGCCCTGTGGACTGAGCAGCGTGGAGGGCGA T C EPG5 Ensembl:ENSG00000152223 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:45850157..45850342 26863196 MeRIP-seq:(Medium) rs956099458 Functional Loss SNV dbSNP153 33..33 33 - - - 91689 RMVar_ID_91689 Human_SNP_ID_646164934 m1A Human chr18 - 45947566 45947566 45947566 TGGATTATAGAAGTCCTTGAAATTAAATGAGGAGTTTAGATTTGATGGTTCCTCTCCCTTACTGC TGGATTATAGAAGTCCTTGAAATTAAATGAGGCGTTTAGATTTGATGGTTCCTCTCCCTTACTGC T G EPG5 Ensembl:ENSG00000152223 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:45947553..45947721 26863196 MeRIP-seq:(Medium) rs1281755650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21350,RMVar_hsa_circ_347352,RMVar_hsa_circ_51118,RMVar_hsa_circ_3668,RMVar_hsa_circ_301805,RMVar_hsa_circ_102266,RMVar_hsa_circ_101895,RMVar_hsa_circ_88048,RMVar_hsa_circ_92520,RMVar_hsa_circ_55488,RMVar_hsa_circ_189858,RMVar_hsa_circ_189859,RMVar_hsa_circ_189856,RMVar_hsa_circ_189857,RMVar_hsa_circ_189866,RMVar_hsa_circ_93976,RMVar_hsa_circ_370801,RMVar_hsa_circ_189865,RMVar_hsa_circ_105795,RMVar_hsa_circ_299190,RMVar_hsa_circ_189870,RMVar_hsa_circ_115268,RMVar_hsa_circ_189872,RMVar_hsa_circ_19154,RMVar_hsa_circ_189871,RMVar_hsa_circ_270507,RMVar_hsa_circ_26536,RMVar_hsa_circ_317057,RMVar_hsa_circ_189874,RMVar_hsa_circ_36696,RMVar_hsa_circ_61307,RMVar_hsa_circ_189876,RMVar_hsa_circ_296569,RMVar_hsa_circ_56507 91690 RMVar_ID_91690 Human_SNP_ID_646168524 m1A Human chr18 + 45961876 45961876 45961876 GTGAGACTCTGTCCCAAAAAAAAAAAAAAAAAACTATCCAGACCACCCATCCTAACCTCTCACCA GTGAGACTCTGTCCCAAAAAAAAAAAAAAAAATCTATCCAGACCACCCATCCTAACCTCTCACCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:45961830..45961957 26863196 MeRIP-seq:(Medium) rs931649349 Functional Loss SNV dbSNP153 33..33 33 - - - 91691 RMVar_ID_91691 Human_SNP_ID_646169959 m1A Human chr18 - 45967267 45967263 45967267 GGTTGCTTGAAGCGCAGGGGTTTGACAAAAACAAACGGTGACGGCGCCGCGGAAGGGTCTATGGC GGTTGCTTGAAGCGCAGGGGTTTGACAAAAAC____GGTGACGGCGCCGCGGAAGGGTCTATGGC CGTTT C EPG5 Ensembl:ENSG00000152223 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:45967171..45967311 26863196 MeRIP-seq:(Medium) rs1305636621 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_4487496 Human_Splice_Rec_1908981,Human_Splice_Rec_1909263 RMVar_hsa_circ_115268,RMVar_hsa_circ_189871 91692 RMVar_ID_91692 Human_SNP_ID_646194772 m1A Human chr18 + 46072236 46072236 46072236 GGCGCGGAGGAGAGCCGGGCCGCAGGTAGCACAGAGCGGGGAGGCCTGACTGCCACTGCCCGCGG GGCGCGGAGGAGAGCCGGGCCGCAGGTAGCACGGAGCGGGGAGGCCTGACTGCCACTGCCCGCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:46072127..46072239 26863196 MeRIP-seq:(Medium) rs949636510 Functional Loss SNV dbSNP153 33..33 33 - - - 91693 RMVar_ID_91693 Human_SNP_ID_646198786 m1A Human chr18 - 46086494 46086494 46086494 CTTGCTAGCGTGCGTATTTCCTTACATTATAGATCTTCTTGGAAACAGAATTGTTCTACAAAGGT CTTGCTAGCGTGCGTATTTCCTTACATTATAGCTCTTCTTGGAAACAGAATTGTTCTACAAAGGT T G ATP5F1A Ensembl:ENSG00000152234 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:46086373..46086523 32194978 MeRIP-seq:(Medium) rs1181393612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906200,Human_RBP_ID_2541493,Human_RBP_ID_17266052,Human_RBP_ID_22446072,Human_RBP_ID_25364145 Human_Splice_Rec_1909414,Human_Splice_Rec_1909436,Human_Splice_Rec_1909460,Human_Splice_Rec_1909482,Human_Splice_Rec_1909504,Human_Splice_Rec_1909526,Human_Splice_Rec_1909544 RMVar_hsa_circ_8625,RMVar_hsa_circ_189886,RMVar_hsa_circ_85740,RMVar_hsa_circ_95736,RMVar_hsa_circ_102670,RMVar_hsa_circ_120046,RMVar_hsa_circ_112686,RMVar_hsa_circ_95343,RMVar_hsa_circ_95451,RMVar_hsa_circ_89868,RMVar_hsa_circ_189890,RMVar_hsa_circ_81920,RMVar_hsa_circ_189888,RMVar_hsa_circ_189889,RMVar_hsa_circ_189887,RMVar_hsa_circ_189882,RMVar_hsa_circ_189884,RMVar_hsa_circ_189885,RMVar_hsa_circ_189883,RMVar_hsa_circ_18970,RMVar_hsa_circ_288593,RMVar_hsa_circ_364062,RMVar_hsa_circ_367349,RMVar_hsa_circ_107520,RMVar_hsa_circ_189893,RMVar_hsa_circ_189894,RMVar_hsa_circ_340143 91694 RMVar_ID_91694 Human_SNP_ID_646198992 m1A Human chr18 - 46087156 46087156 46087156 TGGTCGTGAGGCCTATCCTGGTGATGTGTTCTACCTACACTCCCGGTTGCTGGAGAGAGCAGCCA TGGTCGTGAGGCCTATCCTGGTGATGTGTTCTTCCTACACTCCCGGTTGCTGGAGAGAGCAGCCA T A ATP5F1A Ensembl:ENSG00000152234 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:46087105..46087302 26863196 MeRIP-seq:(Medium) rs779987146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508664,Human_RBP_ID_769118,Human_RBP_ID_906202,Human_RBP_ID_1011942,Human_RBP_ID_1290808,Human_RBP_ID_1549932,Human_RBP_ID_1875727,Human_RBP_ID_3555918,Human_RBP_ID_4495821,Human_RBP_ID_5467926,Human_RBP_ID_8094513,Human_RBP_ID_8471703,Human_RBP_ID_8827304,Human_RBP_ID_9290679,Human_RBP_ID_17265227,Human_RBP_ID_17496480,Human_RBP_ID_17909790,Human_RBP_ID_18191491,Human_RBP_ID_22445889,Human_RBP_ID_22808512,Human_RBP_ID_23771012,Human_RBP_ID_26814418,Human_RBP_ID_26979775,Human_RBP_ID_27265247 Human_Splice_Rec_1909412,Human_Splice_Rec_1909434,Human_Splice_Rec_1909458,Human_Splice_Rec_1909480,Human_Splice_Rec_1909502,Human_Splice_Rec_1909524 Human_miRNA_ID_1960991,Human_miRNA_ID_1960992 RMVar_hsa_circ_8625,RMVar_hsa_circ_189886,RMVar_hsa_circ_85740,RMVar_hsa_circ_95736,RMVar_hsa_circ_102670,RMVar_hsa_circ_120046,RMVar_hsa_circ_112686,RMVar_hsa_circ_95451,RMVar_hsa_circ_89868,RMVar_hsa_circ_81920,RMVar_hsa_circ_189888,RMVar_hsa_circ_189889,RMVar_hsa_circ_189887,RMVar_hsa_circ_189882,RMVar_hsa_circ_189884,RMVar_hsa_circ_189885,RMVar_hsa_circ_189883,RMVar_hsa_circ_288593,RMVar_hsa_circ_364062,RMVar_hsa_circ_367349,RMVar_hsa_circ_107520,RMVar_hsa_circ_189893,RMVar_hsa_circ_189894,RMVar_hsa_circ_340143,RMVar_hsa_circ_4164,RMVar_hsa_circ_357226,RMVar_hsa_circ_189896 91695 RMVar_ID_91695 Human_SNP_ID_646199257 m1A Human chr18 + 46088069 46088069 46088069 GTAGAAGCTATTCTACAATCAGCAGCAATGGGACTTAAGATAATAGCAATGGGACTAAATTTCTT GTAGAAGCTATTCTACAATCAGCAGCAATGGGGCTTAAGATAATAGCAATGGGACTAAATTTCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:46088066..46088303 26863196 MeRIP-seq:(Medium) rs765352396 Functional Loss SNV dbSNP153 33..33 33 - - - 91696 RMVar_ID_91696 Human_SNP_ID_646199331 m1A Human chr18 - 46088256 46088256 46088256 GAAGATTTATATTTACTTTCTCTTTTTAAAGGAAAACCTCAATTGCTATTGACACAATCATTAAC GAAGATTTATATTTACTTTCTCTTTTTAAAGGGAAACCTCAATTGCTATTGACACAATCATTAAC T C ATP5F1A Ensembl:ENSG00000152234 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:46088101..46088316 32194978 MeRIP-seq:(Medium) rs1033367372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51833,Human_RBP_ID_823206,Human_RBP_ID_906205,Human_RBP_ID_3953574,Human_RBP_ID_17266053,Human_RBP_ID_22446079,Human_RBP_ID_22762373 Human_Splice_Rec_1909408,Human_Splice_Rec_1909430,Human_Splice_Rec_1909454,Human_Splice_Rec_1909476,Human_Splice_Rec_1909498,Human_Splice_Rec_1909520,Human_Splice_Rec_1909554,Human_Splice_Rec_1909566 Human_miRNA_ID_2699278,Human_miRNA_ID_2699279 RMVar_hsa_circ_189886,RMVar_hsa_circ_85740,RMVar_hsa_circ_95736,RMVar_hsa_circ_102670,RMVar_hsa_circ_120046,RMVar_hsa_circ_112686,RMVar_hsa_circ_89868,RMVar_hsa_circ_189887,RMVar_hsa_circ_189882,RMVar_hsa_circ_189884,RMVar_hsa_circ_189885,RMVar_hsa_circ_189883,RMVar_hsa_circ_288593,RMVar_hsa_circ_364062,RMVar_hsa_circ_367349,RMVar_hsa_circ_107520,RMVar_hsa_circ_189893,RMVar_hsa_circ_189894,RMVar_hsa_circ_340143,RMVar_hsa_circ_20319,RMVar_hsa_circ_4164,RMVar_hsa_circ_357226,RMVar_hsa_circ_189896,RMVar_hsa_circ_337160,RMVar_hsa_circ_361734,RMVar_hsa_circ_108673,RMVar_hsa_circ_189898,RMVar_hsa_circ_189899 91697 RMVar_ID_91697 Human_SNP_ID_646201461 m1A Human chr18 - 46095074 46095074 46095074 CTTTCATTGCTGCAAGGAACTTCCATGCCTCTAACACTCATCTTCAAAAGACTGGTAAGTTATTA CTTTCATTGCTGCAAGGAACTTCCATGCCTCTGACACTCATCTTCAAAAGACTGGTAAGTTATTA T C ATP5F1A Ensembl:ENSG00000152234 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:46095051..46095075 26863196 MeRIP-seq:(Medium) rs1404974041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508694,Human_RBP_ID_906210,Human_RBP_ID_1011951,Human_RBP_ID_1290810,Human_RBP_ID_1549960,Human_RBP_ID_1875751,Human_RBP_ID_3555938,Human_RBP_ID_4494414,Human_RBP_ID_5421080,Human_RBP_ID_5442400,Human_RBP_ID_6687954,Human_RBP_ID_8094515,Human_RBP_ID_8471727,Human_RBP_ID_9081035,Human_RBP_ID_9258412,Human_RBP_ID_9290685,Human_RBP_ID_13313267,Human_RBP_ID_17265234,Human_RBP_ID_17381042,Human_RBP_ID_17496483,Human_RBP_ID_17693965,Human_RBP_ID_17909797,Human_RBP_ID_18717225,Human_RBP_ID_22446206,Human_RBP_ID_22501179,Human_RBP_ID_22808520,Human_RBP_ID_23277240,Human_RBP_ID_24482736,Human_RBP_ID_26979795,Human_RBP_ID_27265264,Human_RBP_ID_27461402,Human_RBP_ID_27672366 Human_Splice_Rec_1909400,Human_Splice_Rec_1909401,Human_Splice_Rec_1909422,Human_Splice_Rec_1909423,Human_Splice_Rec_1909446,Human_Splice_Rec_1909447,Human_Splice_Rec_1909468,Human_Splice_Rec_1909469,Human_Splice_Rec_1909490,Human_Splice_Rec_1909491,Human_Splice_Rec_1909512,Human_Splice_Rec_1909513,Human_Splice_Rec_1909538,Human_Splice_Rec_1909539,Human_Splice_Rec_1909548,Human_Splice_Rec_1909549,Human_Splice_Rec_1909558,Human_Splice_Rec_1909559,Human_Splice_Rec_1909574,Human_Splice_Rec_1909575,Human_Splice_Rec_1909582,Human_Splice_Rec_1909583,Human_Splice_Rec_1909592,Human_Splice_Rec_1909593,Human_Splice_Rec_1909598,Human_Splice_Rec_1909599,Human_Splice_Rec_1909604,Human_Splice_Rec_1909605,Human_Splice_Rec_1909610,Human_Splice_Rec_1909611,Human_Splice_Rec_1909618,Human_Splice_Rec_1909619,Human_Splice_Rec_1909622 RMVar_hsa_circ_120046,RMVar_hsa_circ_89868,RMVar_hsa_circ_189882,RMVar_hsa_circ_189883,RMVar_hsa_circ_288593,RMVar_hsa_circ_189894,RMVar_hsa_circ_340143,RMVar_hsa_circ_357226,RMVar_hsa_circ_189896,RMVar_hsa_circ_337160,RMVar_hsa_circ_189899,RMVar_hsa_circ_76524,RMVar_hsa_circ_44303,RMVar_hsa_circ_189901,RMVar_hsa_circ_371351,RMVar_hsa_circ_189903,RMVar_hsa_circ_189904,RMVar_hsa_circ_370107 91698 RMVar_ID_91698 Human_SNP_ID_646202512 m1A Human chr18 + 46098221 46098221 46098221 GAAGGGCGCGGACCACGGCCGCAGCAACGCGCACGGACAGCATCTTTGCAGTTACTCCGCAGGCG GAAGGGCGCGGACCACGGCCGCAGCAACGCGCCCGGACAGCATCTTTGCAGTTACTCCGCAGGCG A C NONHSAG023781.2 RNACentral:URS00008B48EE lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:46098151..46098225 26863196 MeRIP-seq:(Medium) rs780078808 Functional Loss SNV dbSNP153 33..33 33 - - - 91699 RMVar_ID_91699 Human_SNP_ID_646202517 m1A Human chr18 + 46098225 46098225 46098225 GGCGCGGACCACGGCCGCAGCAACGCGCACGGACAGCATCTTTGCAGTTACTCCGCAGGCGGTAC GGCGCGGACCACGGCCGCAGCAACGCGCACGGGCAGCATCTTTGCAGTTACTCCGCAGGCGGTAC A G NONHSAG023781.2 RNACentral:URS00008B48EE lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:46098116..46098225 26863196 MeRIP-seq:(Medium) rs758593789 Functional Loss SNV dbSNP153 33..33 33 - - - 91700 RMVar_ID_91700 Human_SNP_ID_646202551 m1A Human chr18 - 46098261 46098261 46098261 TTTGTCCCAGTCAGTCCGGAGGCTGCGGCTGCAGAAGTACCGCCTGCGGAGTAACTGCAAAGATG TTTGTCCCAGTCAGTCCGGAGGCTGCGGCTGCGGAAGTACCGCCTGCGGAGTAACTGCAAAGATG T C ATP5F1A Ensembl:ENSG00000152234 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:46098226..46098275 32194978 MeRIP-seq:(Medium) rs367797793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51841,Human_RBP_ID_508698,Human_RBP_ID_769128,Human_RBP_ID_823344,Human_RBP_ID_1011953,Human_RBP_ID_4487625,Human_RBP_ID_5319534,Human_RBP_ID_5442401,Human_RBP_ID_5468135,Human_RBP_ID_8828885,Human_RBP_ID_9290688,Human_RBP_ID_9327762,Human_RBP_ID_17693966,Human_RBP_ID_17909798,Human_RBP_ID_18420780,Human_RBP_ID_18717232,Human_RBP_ID_22064238,Human_RBP_ID_22445895 Human_Splice_Rec_1909399,Human_Splice_Rec_1909444,Human_Splice_Rec_1909445,Human_Splice_Rec_1909467,Human_Splice_Rec_1909489,Human_Splice_Rec_1909537,Human_Splice_Rec_1909547,Human_Splice_Rec_1909572,Human_Splice_Rec_1909573,Human_Splice_Rec_1909597,Human_Splice_Rec_1909617,Human_Splice_Rec_1909621 RMVar_hsa_circ_120046,RMVar_hsa_circ_189882,RMVar_hsa_circ_76524,RMVar_hsa_circ_189901 91701 RMVar_ID_91701 Human_SNP_ID_646202552 m1A Human chr18 - 46098261 46098261 46098261 TTTGTCCCAGTCAGTCCGGAGGCTGCGGCTGCAGAAGTACCGCCTGCGGAGTAACTGCAAAGATG TTTGTCCCAGTCAGTCCGGAGGCTGCGGCTGCCGAAGTACCGCCTGCGGAGTAACTGCAAAGATG T G ATP5F1A Ensembl:ENSG00000152234 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:46098226..46098275 32194978 MeRIP-seq:(Medium) rs367797793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51841,Human_RBP_ID_508698,Human_RBP_ID_769128,Human_RBP_ID_823344,Human_RBP_ID_1011953,Human_RBP_ID_4487625,Human_RBP_ID_5319534,Human_RBP_ID_5442401,Human_RBP_ID_5468135,Human_RBP_ID_8828885,Human_RBP_ID_9290688,Human_RBP_ID_9327762,Human_RBP_ID_17693966,Human_RBP_ID_17909798,Human_RBP_ID_18420780,Human_RBP_ID_18717232,Human_RBP_ID_22064238,Human_RBP_ID_22445895 Human_Splice_Rec_1909399,Human_Splice_Rec_1909444,Human_Splice_Rec_1909445,Human_Splice_Rec_1909467,Human_Splice_Rec_1909489,Human_Splice_Rec_1909537,Human_Splice_Rec_1909547,Human_Splice_Rec_1909572,Human_Splice_Rec_1909573,Human_Splice_Rec_1909597,Human_Splice_Rec_1909617,Human_Splice_Rec_1909621 RMVar_hsa_circ_120046,RMVar_hsa_circ_189882,RMVar_hsa_circ_76524,RMVar_hsa_circ_189901 91702 RMVar_ID_91702 Human_SNP_ID_646202590 m1A Human chr18 + 46098301 46098301 46098301 CAGCCTCCGGACTGACTGGGACAAAATGGCCGAGCCGCAAAGAAGGTCAAGACAGCCGGCCCACC CAGCCTCCGGACTGACTGGGACAAAATGGCCGGGCCGCAAAGAAGGTCAAGACAGCCGGCCCACC A G NONHSAG023781.2 RNACentral:URS00008B48EE lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:46098251..46098300 26863196 MeRIP-seq:(Medium) rs1568256704 Functional Loss SNV dbSNP153 33..33 33 - - - 91703 RMVar_ID_91703 Human_SNP_ID_646222115 m1A Human chr18 - 46174132 46174132 46174132 CGCGGTCAGAGCCCCTGCCGGGACCAAAGTGAACCTCGCCGCCTCCGCAGCCTCTACCACCAAGT CGCGGTCAGAGCCCCTGCCGGGACCAAAGTGATCCTCGCCGCCTCCGCAGCCTCTACCACCAAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:46174082..46174262 26863196 MeRIP-seq:(Medium) rs1295133876 Functional Loss SNV dbSNP153 33..33 33 - - - 91704 RMVar_ID_91704 Human_SNP_ID_646260811 m1A Human chr18 + 46334093 46334093 46334093 CGCCTTTGAATGTCGAGAGGGGCCGGGAAGGGAGCCTTTCCATGGGCCATCTGTCTCCCCGCCAG CGCCTTTGAATGTCGAGAGGGGCCGGGAAGGGGGCCTTTCCATGGGCCATCTGTCTCCCCGCCAG A G RNF165 Ensembl:ENSG00000141622 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:46334057..46334326 26863196 MeRIP-seq:(Medium) rs1447968049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1909783 91705 RMVar_ID_91705 Human_SNP_ID_646293365 m1A Human chr18 + 46460920 46460920 46460920 CTTGCTACACTTGGCACCCCCCCGCCCCCACCACAACCCTGCCTCTCCATCATGAACCTGCCTTT CTTGCTACACTTGGCACCCCCCCGCCCCCACCCCAACCCTGCCTCTCCATCATGAACCTGCCTTT A C RNF165 Ensembl:ENSG00000141622 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:46460825..46461004 26863410 MeRIP-seq:(Medium) rs1459778916 Functional Loss SNV dbSNP153 33..33 33 - - - 91706 RMVar_ID_91706 Human_SNP_ID_646293366 m1A Human chr18 + 46460920 46460920 46460920 CTTGCTACACTTGGCACCCCCCCGCCCCCACCACAACCCTGCCTCTCCATCATGAACCTGCCTTT CTTGCTACACTTGGCACCCCCCCGCCCCCACCGCAACCCTGCCTCTCCATCATGAACCTGCCTTT A G RNF165 Ensembl:ENSG00000141622 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:46460825..46461004 26863410 MeRIP-seq:(Medium) rs1459778916 Functional Loss SNV dbSNP153 33..33 33 - - - 91707 RMVar_ID_91707 Human_SNP_ID_646405959 m1A Human chr18 + 46917354 46917354 46917354 CCTCAACTCTTCGAAATCCGCCATTTTATACCACCCGCGGGCGCCGCCGCCGCTGCCGCCGCACC CCTCAACTCTTCGAAATCCGCCATTTTATACCCCCCGCGGGCGCCGCCGCCGCTGCCGCCGCACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:46917301..46917478;chr18:46917204..46917500 26863196 MeRIP-seq:(Medium) rs764993407 Functional Loss SNV dbSNP153 33..33 33 - - - 91708 RMVar_ID_91708 Human_SNP_ID_646405971 m1A Human chr18 - 46917375 46917366 46917375 TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCAGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGC_________GGCGCCCGCGGGTGGTATAAAATG CGCCGCCGCT C PIAS2 Ensembl:ENSG00000078043 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr18:46917322..46917440;chr18:46917326..46917475 26863196 MeRIP-seq:(Medium) rs1233204363 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_822967,Human_RBP_ID_4494008,Human_RBP_ID_9327871 Human_Splice_Rec_1910413,Human_Splice_Rec_1910439,Human_Splice_Rec_1910463,Human_Splice_Rec_1910487,Human_Splice_Rec_1910531,Human_Splice_Rec_1910595,Human_Splice_Rec_1910601 RMVar_hsa_circ_88083,RMVar_hsa_circ_189935 91709 RMVar_ID_91709 Human_SNP_ID_646405980 m1A Human chr18 - 46917375 46917375 46917375 TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCAGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCGGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG T C PIAS2 Ensembl:ENSG00000078043 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr18:46917322..46917440;chr18:46917326..46917475 26863196 MeRIP-seq:(Medium) rs978866399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822967,Human_RBP_ID_4494008,Human_RBP_ID_9327871 Human_Splice_Rec_1910413,Human_Splice_Rec_1910439,Human_Splice_Rec_1910463,Human_Splice_Rec_1910487,Human_Splice_Rec_1910531,Human_Splice_Rec_1910595,Human_Splice_Rec_1910601 RMVar_hsa_circ_88083,RMVar_hsa_circ_189935 91710 RMVar_ID_91710 Human_SNP_ID_646405981 m1A Human chr18 - 46917375 46917375 46917375 TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCAGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCCGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG T G PIAS2 Ensembl:ENSG00000078043 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr18:46917322..46917440;chr18:46917326..46917475 26863196 MeRIP-seq:(Medium) rs978866399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822967,Human_RBP_ID_4494008,Human_RBP_ID_9327871 Human_Splice_Rec_1910413,Human_Splice_Rec_1910439,Human_Splice_Rec_1910463,Human_Splice_Rec_1910487,Human_Splice_Rec_1910531,Human_Splice_Rec_1910595,Human_Splice_Rec_1910601 RMVar_hsa_circ_88083,RMVar_hsa_circ_189935 91711 RMVar_ID_91711 Human_SNP_ID_646406000 m1A Human chr18 + 46917404 46917404 46917404 CGCTGCCGCCGCACCCACTCCCGCTGCCGCCAACGACGCTGCCGCCACCACGGCCGCCGCCGCCT CGCTGCCGCCGCACCCACTCCCGCTGCCGCCAGCGACGCTGCCGCCACCACGGCCGCCGCCGCCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:46917320..46917464 26863196 MeRIP-seq:(Medium) rs1487720191 Functional Loss SNV dbSNP153 33..33 33 - - - 91712 RMVar_ID_91712 Human_SNP_ID_646406176 m1A Human chr18 + 46917780 46917780 46917780 GCGGGCCTGGCCTCGGGAAGTGGCGGGGAGGAAGAAGAGGCGGCCGGGACGCGTGACAGGAGCAT GCGGGCCTGGCCTCGGGAAGTGGCGGGGAGGATGAAGAGGCGGCCGGGACGCGTGACAGGAGCAT A T KATNAL2 Ensembl:ENSG00000167216 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:46917618..46917861 26863196 MeRIP-seq:(Medium) rs989659738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_52318,Human_RBP_ID_4487821 91713 RMVar_ID_91713 Human_SNP_ID_646413502 m1A Human chr18 + 46946186 46946186 46946186 GAATAGGATTCACAGCAAGAGAGACAGAAGGGAAAGACATTGAAGAAACAGACTAGTTAACACAT GAATAGGATTCACAGCAAGAGAGACAGAAGGGGAAGACATTGAAGAAACAGACTAGTTAACACAT A G KATNAL2 Ensembl:ENSG00000167216 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:46946079..46946206 26863196 MeRIP-seq:(Medium) rs773665932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2542138 Human_Splice_Rec_1910607 RMVar_hsa_circ_189960,RMVar_hsa_circ_282130 91714 RMVar_ID_91714 Human_SNP_ID_646413765 m1A Human chr18 - 46947150 46947150 46947150 TCAGGAACCGACCCTGCCGTCCCTTTCATCCGACCCGTTGTCACCCCCAAACCCGCCTGTGTCTC TCAGGAACCGACCCTGCCGTCCCTTTCATCCGCCCCGTTGTCACCCCCAAACCCGCCTGTGTCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:46947106..46947226 26863196 MeRIP-seq:(Medium) rs887920191 Functional Loss SNV dbSNP153 33..33 33 - - - 91715 RMVar_ID_91715 Human_SNP_ID_646447723 m1A Human chr18 - 47136451 47136451 47136451 AACTGTATTTTTAATTTCATTTGCTCTCTCCTAGGGAATGAAGGATGGCAGCATGCCGTGCATTA AACTGTATTTTTAATTTCATTTGCTCTCTCCTGGGGAATGAAGGATGGCAGCATGCCGTGCATTA T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:47136413..47136508 26863196 MeRIP-seq:(Medium) rs200622348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_550 91716 RMVar_ID_91716 Human_SNP_ID_646451315 m1A Human chr18 - 47150395 47150395 47150395 GGCTTTGCCATTAGCGGGGGCCTTTCCTGAGGACGGCGTACGGAGTGTGGGTGAGAAGCCGCTGT GGCTTTGCCATTAGCGGGGGCCTTTCCTGAGGGCGGCGTACGGAGTGTGGGTGAGAAGCCGCTGT T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:47150385..47150470 26863410 MeRIP-seq:(Medium) rs544846876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494216,Human_RBP_ID_9379602,Human_RBP_ID_18420666,Human_RBP_ID_22064241,Human_RBP_ID_22965725 Human_Splice_Rec_1910723,Human_Splice_Rec_1910735,Human_Splice_Rec_1910745,Human_Splice_Rec_1910751,Human_Splice_Rec_1910759,Human_Splice_Rec_1910765,Human_Splice_Rec_1910773,Human_Splice_Rec_1910789,Human_Splice_Rec_1910795,Human_Splice_Rec_1910801 91717 RMVar_ID_91717 Human_SNP_ID_646451336 m1A Human chr18 + 47150438 47150438 47150438 GGCCCCCGCTAATGGCAAAGCCAGCCACCCGCACTGGCCGCGGGTCCTCAGCCGGGATAGACAGC GGCCCCCGCTAATGGCAAAGCCAGCCACCCGCGCTGGCCGCGGGTCCTCAGCCGGGATAGACAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:47150282..47150500;chr18:47150256..47150470 26863196 MeRIP-seq:(Medium) rs1265683307 Functional Loss SNV dbSNP153 33..33 33 - - - 91718 RMVar_ID_91718 Human_SNP_ID_646453217 m1A Human chr18 + 47157512 47157512 47157512 GATTTAATTCCCGGCTCTTCTCCAAATCCACCAATTCCCTGGTCTGTTCCCCAGCCAACTGTATA GATTTAATTCCCGGCTCTTCTCCAAATCCACCGATTCCCTGGTCTGTTCCCCAGCCAACTGTATA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:47157451..47176295 32194978 MeRIP-seq:(Medium) rs754658292 Functional Loss SNV dbSNP153 33..33 33 - - - 91719 RMVar_ID_91719 Human_SNP_ID_646453218 m1A Human chr18 + 47157512 47157512 47157512 GATTTAATTCCCGGCTCTTCTCCAAATCCACCAATTCCCTGGTCTGTTCCCCAGCCAACTGTATA GATTTAATTCCCGGCTCTTCTCCAAATCCACCTATTCCCTGGTCTGTTCCCCAGCCAACTGTATA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:47157451..47176295 32194978 MeRIP-seq:(Medium) rs754658292 Functional Loss SNV dbSNP153 33..33 33 - - - 91720 RMVar_ID_91720 Human_SNP_ID_646457545 m1A Human chr18 + 47176276 47176276 47176276 CTGCCTGCAGCAGTGAGTACAGGGTAAAGGCCATGGCCGTCCGAGGCCGCCCCGAAGTCCAAGCG CTGCCTGCAGCAGTGAGTACAGGGTAAAGGCCGTGGCCGTCCGAGGCCGCCCCGAAGTCCAAGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:47176176..47176375 26863196 MeRIP-seq:(Medium) rs983642731 Functional Loss SNV dbSNP153 33..33 33 - - - 91721 RMVar_ID_91721 Human_SNP_ID_646457546 m1A Human chr18 + 47176276 47176276 47176276 CTGCCTGCAGCAGTGAGTACAGGGTAAAGGCCATGGCCGTCCGAGGCCGCCCCGAAGTCCAAGCG CTGCCTGCAGCAGTGAGTACAGGGTAAAGGCCTTGGCCGTCCGAGGCCGCCCCGAAGTCCAAGCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:47176176..47176375 26863196 MeRIP-seq:(Medium) rs983642731 Functional Loss SNV dbSNP153 33..33 33 - - - 91722 RMVar_ID_91722 Human_SNP_ID_646457547 m1A Human chr18 - 47176277 47176277 47176277 TCGCTTGGACTTCGGGGCGGCCTCGGACGGCCATGGCCTTTACCCTGTACTCACTGCTGCAGGCA TCGCTTGGACTTCGGGGCGGCCTCGGACGGCCTTGGCCTTTACCCTGTACTCACTGCTGCAGGCA T A AC012254.2,IER3IP1 Ensembl:ENSG00000267228,Ensembl:ENSG00000134049 Protein coding,Protein coding start codon,start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:47157497..47176354 26863410 MeRIP-seq:(Medium) rs1200072625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508915,Human_RBP_ID_1012009,Human_RBP_ID_1290865,Human_RBP_ID_1550153,Human_RBP_ID_4487893,Human_RBP_ID_5238104,Human_RBP_ID_5319609,Human_RBP_ID_5467936,Human_RBP_ID_8471935,Human_RBP_ID_9081289,Human_RBP_ID_9327766,Human_RBP_ID_9379867,Human_RBP_ID_22445974,Human_RBP_ID_22965674 Human_Splice_Rec_1910805,Human_Splice_Rec_1910815,Human_Splice_Rec_1910819,Human_Splice_Rec_1910827,Human_Splice_Rec_1910831 91723 RMVar_ID_91723 Human_SNP_ID_646472973 m1A Human chr18 + 47247066 47247066 47247066 AGAAGGCCTCGGTGGTGCGGGTGCTGGGCCAGAGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG AGAAGGCCTCGGTGGTGCGGGTGCTGGGCCAGGGGGGGCGGCGGGGGCGGCGGCGGCGGCGGCGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:47246977..47247105 26863196 MeRIP-seq:(Medium) rs1448142690 Functional Loss SNV dbSNP153 33..33 33 - - - 91724 RMVar_ID_91724 Human_SNP_ID_646623406 m1A Human chr18 - 47835823 47835823 47835823 TCCAAATATGCTCTTTGATTTACTTATTTTTAATTAAAGATGGTAATTTATTGAACAATGAAATC TCCAAATATGCTCTTTGATTTACTTATTTTTAGTTAAAGATGGTAATTTATTGAACAATGAAATC T C SMAD2 Ensembl:ENSG00000175387 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1792671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2542675,Human_RBP_ID_6689708,Human_RBP_ID_22390559,Human_RBP_ID_27672522 GWAS_ID_11859,GWAS_ID_11860,GWAS_ID_11861 RMVar_hsa_circ_189980,RMVar_hsa_circ_189979,RMVar_hsa_circ_85065,RMVar_hsa_circ_267989 91725 RMVar_ID_91725 Human_SNP_ID_646640912 m1A Human chr18 - 47896644 47896642 47896645 AGCAGGCGGAGGAGAGCAGAATGGGCAGGAAGAAAAGTGGTGTGAGAAAGCAGTGAAAAGTCTGG AGCAGGCGGAGGAGAGCAGAATGGGCAGGAA___AAGTGGTGTGAGAAAGCAGTGAAAAGTCTGG TTTC T SMAD2 Ensembl:ENSG00000175387 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr18:47896551..47896764;chr18:47896576..47896775 26863196 MeRIP-seq:(Medium) rs1478723784 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_52131,Human_RBP_ID_509011,Human_RBP_ID_2543368,Human_RBP_ID_3953578,Human_RBP_ID_9379606,Human_RBP_ID_23771913 Human_miRNA_ID_2451057,Human_miRNA_ID_2451058,Human_miRNA_ID_2451059 RMVar_hsa_circ_189979,RMVar_hsa_circ_267989,RMVar_hsa_circ_189985,RMVar_hsa_circ_189982,RMVar_hsa_circ_189983,RMVar_hsa_circ_328037,RMVar_hsa_circ_189986,RMVar_hsa_circ_374009,RMVar_hsa_circ_189992,RMVar_hsa_circ_289782,RMVar_hsa_circ_189995,RMVar_hsa_circ_277105,RMVar_hsa_circ_189996,RMVar_hsa_circ_315585,RMVar_hsa_circ_111810,RMVar_hsa_circ_190003,RMVar_hsa_circ_375058,RMVar_hsa_circ_190004,RMVar_hsa_circ_63495,RMVar_hsa_circ_104260,RMVar_hsa_circ_190005,RMVar_hsa_circ_190006,RMVar_hsa_circ_321247,RMVar_hsa_circ_60536 91726 RMVar_ID_91726 Human_SNP_ID_646640946 m1A Human chr18 + 47896776 47896776 47896776 AGATGGACGACATGTTCTTACCAAAGGCAGCAAGCCACGCTAGGAAAACAGCCTCTTGTATCGAA AGATGGACGACATGTTCTTACCAAAGGCAGCAGGCCACGCTAGGAAAACAGCCTCTTGTATCGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:47896726..47896825 32194978 MeRIP-seq:(Medium) rs1199546610 Functional Loss SNV dbSNP153 33..33 33 - - - 91727 RMVar_ID_91727 Human_SNP_ID_646643586 m1A Human chr18 - 47906761 47906756 47906761 AGAGCACAAGCTAAGGGAAGGGAGCACAAGCTAAAGACTACAGGTAACCACTAGAAGCTGAAAAA AGAGCACAAGCTAAGGGAAGGGAGCACAAGCT_____CTACAGGTAACCACTAGAAGCTGAAAAA GTCTTT G SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:47906759..47906900 26863196 MeRIP-seq:(Medium) rs1371053082 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_111810,RMVar_hsa_circ_63495,RMVar_hsa_circ_190005,RMVar_hsa_circ_60536 91728 RMVar_ID_91728 Human_SNP_ID_646649984 m1A Human chr18 + 47930162 47930162 47930162 AGGCAGCCCCCGCCCCCGTCAGCCTGGGCGGCAGCGCAGTGCAACCGAGCCCCGTCCCTTCCCGG AGGCAGCCCCCGCCCCCGTCAGCCTGGGCGGCCGCGCAGTGCAACCGAGCCCCGTCCCTTCCCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:47930157..47930372 26863196 MeRIP-seq:(Medium) rs549125286 Functional Loss SNV dbSNP153 33..33 33 - - - 91729 RMVar_ID_91729 Human_SNP_ID_646649990 m1A Human chr18 - 47930188 47930188 47930188 GGGCGTGCGGGTTCGGGGCCGGAGAGCCGGGAAGGGACGGGGCTCGGTTGCACTGCGCTGCCGCC GGGCGTGCGGGTTCGGGGCCGGAGAGCCGGGAGGGGACGGGGCTCGGTTGCACTGCGCTGCCGCC T C SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:47930183..47930354 26863196 MeRIP-seq:(Medium) rs1263920803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238673,Human_RBP_ID_1067065,Human_RBP_ID_3561110,Human_RBP_ID_5144681,Human_RBP_ID_5238137,Human_RBP_ID_5369386,Human_RBP_ID_8194112,Human_RBP_ID_18460772,Human_RBP_ID_18944042,Human_RBP_ID_24559607 RMVar_hsa_circ_111810,RMVar_hsa_circ_190005,RMVar_hsa_circ_60536 91730 RMVar_ID_91730 Human_SNP_ID_646650351 m1A Human chr18 - 47930826 47930826 47930826 GCGCGGCCGCGGCGGCGGAGAAGCAGCTCGCCAGCCAGCAGCCCGCCAGCCGCCGGGAGGTGGGT GCGCGGCCGCGGCGGCGGAGAAGCAGCTCGCCTGCCAGCAGCCCGCCAGCCGCCGGGAGGTGGGT T A SMAD2 Ensembl:ENSG00000175387 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:47930801..47931135 26863196 MeRIP-seq:(Medium) rs972051197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4488019 Human_Splice_Rec_1910907,Human_Splice_Rec_1910927,Human_Splice_Rec_1910961,Human_Splice_Rec_1910993,Human_Splice_Rec_1911013 91731 RMVar_ID_91731 Human_SNP_ID_646650352 m1A Human chr18 - 47930826 47930826 47930826 GCGCGGCCGCGGCGGCGGAGAAGCAGCTCGCCAGCCAGCAGCCCGCCAGCCGCCGGGAGGTGGGT GCGCGGCCGCGGCGGCGGAGAAGCAGCTCGCCCGCCAGCAGCCCGCCAGCCGCCGGGAGGTGGGT T G SMAD2 Ensembl:ENSG00000175387 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:47930801..47931135 26863196 MeRIP-seq:(Medium) rs972051197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4488019 Human_Splice_Rec_1910907,Human_Splice_Rec_1910927,Human_Splice_Rec_1910961,Human_Splice_Rec_1910993,Human_Splice_Rec_1911013 91732 RMVar_ID_91732 Human_SNP_ID_646650430 m1A Human chr18 + 47931034 47931034 47931034 GGGTATGGAAGACGGAGGGAGCGGAGGAGGAAAGGAACGAGGCCGAGCACCGCGGGAAGGGCCGG GGGTATGGAAGACGGAGGGAGCGGAGGAGGAAGGGAACGAGGCCGAGCACCGCGGGAAGGGCCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:47930999..47931155 26863196 MeRIP-seq:(Medium) rs977075738 Functional Loss SNV dbSNP153 33..33 33 - - - 91733 RMVar_ID_91733 Human_SNP_ID_646797327 m1A Human chr18 - 48539191 48539191 48539191 AGCCGACTCCTGCCTCGAGTTCGGAGCGTCCCAGCTGCGGAGGGGATCGGGCGCCCCAGCGCACA AGCCGACTCCTGCCTCGAGTTCGGAGCGTCCCCGCTGCGGAGGGGATCGGGCGCCCCAGCGCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:48539060..48539275 26863196 MeRIP-seq:(Medium) rs958695534 Functional Loss SNV dbSNP153 33..33 33 - - - 91734 RMVar_ID_91734 Human_SNP_ID_646797346 m1A Human chr18 + 48539270 48539270 48539270 CCCTCCCTTCCCCTTCCCTGCCCCCTTCCCCCACCCCCGACTCGGGCTTGGCGCGGCGGCCAGAG CCCTCCCTTCCCCTTCCCTGCCCCCTTCCCCCCCCCCCGACTCGGGCTTGGCGCGGCGGCCAGAG A C CTIF Ensembl:ENSG00000134030 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:48539076..48539300 26863196 MeRIP-seq:(Medium) rs1336472061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369387,Human_RBP_ID_17910176,Human_RBP_ID_18420668,Human_RBP_ID_18944046,Human_RBP_ID_18993397 Human_Splice_Rec_1911261,Human_Splice_Rec_1911283,Human_Splice_Rec_1911307 91735 RMVar_ID_91735 Human_SNP_ID_646797704 m1A Human chr18 - 48540439 48540439 48540439 CGGTGTCCCGGACGCCCCCTCCGGCCACATCCAGGCACCGGCACGCGGCCCTCCGAGGCCCCAGA CGGTGTCCCGGACGCCCCCTCCGGCCACATCCGGGCACCGGCACGCGGCCCTCCGAGGCCCCAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48540435..48540662 26863196 MeRIP-seq:(Medium) rs914540095 Functional Loss SNV dbSNP153 33..33 33 - - - 91736 RMVar_ID_91736 Human_SNP_ID_646798895 m1A Human chr18 + 48545092 48545092 48545092 GCTGAATCTTAATGGATGAAAAGGAACTGGCCAGGAAAGGAGATGGGAGACGGGCATTCAGGGAG GCTGAATCTTAATGGATGAAAAGGAACTGGCCGGGAAAGGAGATGGGAGACGGGCATTCAGGGAG A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48544983..48545295 26863196 MeRIP-seq:(Medium) rs935940042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190008,RMVar_hsa_circ_99195 91737 RMVar_ID_91737 Human_SNP_ID_646808311 m1A Human chr18 - 48582119 48582119 48582119 GGTGATTACAGCACCACACTCTCAGGGTACCCAGCCCCCACACCCCACCACGCCTCCCACTTCTT GGTGATTACAGCACCACACTCTCAGGGTACCCGGCCCCCACACCCCACCACGCCTCCCACTTCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48582114..48582322 26863196 MeRIP-seq:(Medium) rs1257668255 Functional Loss SNV dbSNP153 33..33 33 - - - 91738 RMVar_ID_91738 Human_SNP_ID_646813798 m1A Human chr18 - 48602945 48602942 48602946 CCCATTCATCCATCCATCCATCCACTCATCTAACTGTCCATTCACCCACCCACCTGTCTAGCCAT CCCATTCATCCATCCATCCATCCACTCATCT____GTCCATTCACCCACCCACCTGTCTAGCCAT CAGTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48602709..48603073 26863196 MeRIP-seq:(Medium) rs1357580755 Functional Loss DEL dbSNP153 32..35 33 - - - 91739 RMVar_ID_91739 Human_SNP_ID_646813951 m1A Human chr18 + 48603333 48603333 48603333 ATGGGTAGATGGATGGTTGGATGGATACATGAATGGGTGGATTGGGATGGACGGCTAGATAGGTG ATGGGTAGATGGATGGTTGGATGGATACATGAGTGGGTGGATTGGGATGGACGGCTAGATAGGTG A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48603188..48603464 26863196 MeRIP-seq:(Medium) rs1315859474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8194125 RMVar_hsa_circ_190008,RMVar_hsa_circ_99195 91740 RMVar_ID_91740 Human_SNP_ID_646814192 m1A Human chr18 - 48603721 48603721 48603721 TGGTGCAGCTCCAGCCAGCCAGCAAGCCAGCCACCCATCTATATCTATTCATCCATCCATCCACC TGGTGCAGCTCCAGCCAGCCAGCAAGCCAGCCGCCCATCTATATCTATTCATCCATCCATCCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:48603642..48603747 26863196 MeRIP-seq:(Medium) rs978263480 Functional Loss SNV dbSNP153 33..33 33 - - - 91741 RMVar_ID_91741 Human_SNP_ID_646819031 m1A Human chr18 + 48622054 48622054 48622054 GGCCACGAAGGTGCAGAGGCAGAGTTACAAAGATGACTTTAACCAGGGTGGAGGTTTCTCCAGGG GGCCACGAAGGTGCAGAGGCAGAGTTACAAAGGTGACTTTAACCAGGGTGGAGGTTTCTCCAGGG A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48622043..48622525 26863196 MeRIP-seq:(Medium) rs1568080741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63209,RMVar_hsa_circ_190008,RMVar_hsa_circ_99195,RMVar_hsa_circ_296459,RMVar_hsa_circ_369384,RMVar_hsa_circ_65344,RMVar_hsa_circ_190011,RMVar_hsa_circ_190012,RMVar_hsa_circ_190010 91742 RMVar_ID_91742 Human_SNP_ID_646819063 m1A Human chr18 - 48622213 48622213 48622213 TTACAATTCTTTGGGTGGCCTCCAATCCACTGACCCTACCACCTGTCAGCCTCCACAACCACCTC TTACAATTCTTTGGGTGGCCTCCAATCCACTGGCCCTACCACCTGTCAGCCTCCACAACCACCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48621997..48622521 26863196 MeRIP-seq:(Medium) rs904344773 Functional Loss SNV dbSNP153 33..33 33 - - - 91743 RMVar_ID_91743 Human_SNP_ID_646820645 m1A Human chr18 - 48627845 48627845 48627845 TGGCCACTCCCTCTGCCTGGATACCCTTTCCCAGGTGGCCTCACTCTCACCTCCTTCAAATCCTC TGGCCACTCCCTCTGCCTGGATACCCTTTCCCGGGTGGCCTCACTCTCACCTCCTTCAAATCCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:48627821..48628061 26863196 MeRIP-seq:(Medium) rs949447714 Functional Loss SNV dbSNP153 33..33 33 - - - 91744 RMVar_ID_91744 Human_SNP_ID_646847921 m1A Human chr18 - 48730341 48730327 48730341 CGCAGGGGCCCCTCACACAGCAGGAGCCCCTCACACCGCAGGGGCCCCTCACACCGCAGAAGCCC CGCAGGGGCCCCTCACACAGCAGGAGCCCCTC______________CCTCACACCGCAGAAGCCC GGGCCCCTGCGGTGT G HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr18:48730307..48730420;chr18:48730292..48730508 26863196 MeRIP-seq:(Medium) rs1473434195 Functional Loss DEL dbSNP153 33..46 33 - - - 91745 RMVar_ID_91745 Human_SNP_ID_646847953 m1A Human chr18 - 48730352 48730352 48730352 GCCCCTCACACCGCAGGGGCCCCTCACACAGCAGGAGCCCCTCACACCGCAGGGGCCCCTCACAC GCCCCTCACACCGCAGGGGCCCCTCACACAGCGGGAGCCCCTCACACCGCAGGGGCCCCTCACAC T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48730023..48731016 26863196 MeRIP-seq:(Medium) rs986792490 Functional Loss SNV dbSNP153 33..33 33 - - - 91746 RMVar_ID_91746 Human_SNP_ID_646848075 m1A Human chr18 + 48730451 48730451 48730451 GCCCCTGCGCTGTGAGGGGCCCCTGTGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTTCCGCGGT GCCCCTGCGCTGTGAGGGGCCCCTGTGGTGTGTGGGGCTTCCGCGGTGTGAGGGGCTTCCGCGGT A T CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730223..48730474 26863196 MeRIP-seq:(Medium) rs28548123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17130834 RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91747 RMVar_ID_91747 Human_SNP_ID_646848077 m1A Human chr18 - 48730458 48730456 48730458 CCCTCACACCGCGGAAGCCCCTCACACCGCGGAAGCCCCTCACACCACAGGGGCCCCTCACAGCG CCCTCACACCGCGGAAGCCCCTCACACCGCGG__GCCCCTCACACCACAGGGGCCCCTCACAGCG CTT C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:48729997..48731089 26863196 MeRIP-seq:(Medium) rs1416937201 Functional Loss DEL dbSNP153 33..34 33 - - - 91748 RMVar_ID_91748 Human_SNP_ID_646848079 m1A Human chr18 - 48730458 48730458 48730458 CCCTCACACCGCGGAAGCCCCTCACACCGCGGAAGCCCCTCACACCACAGGGGCCCCTCACAGCG CCCTCACACCGCGGAAGCCCCTCACACCGCGGGAGCCCCTCACACCACAGGGGCCCCTCACAGCG T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:48729997..48731089 26863196 MeRIP-seq:(Medium) rs1377933784 Functional Loss SNV dbSNP153 33..33 33 - - - 91749 RMVar_ID_91749 Human_SNP_ID_646848089 m1A Human chr18 - 48730465 48730465 48730465 CAGAAGCCCCTCACACCGCGGAAGCCCCTCACACCGCGGAAGCCCCTCACACCACAGGGGCCCCT CAGAAGCCCCTCACACCGCGGAAGCCCCTCACGCCGCGGAAGCCCCTCACACCACAGGGGCCCCT T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48729997..48731070 26863196 MeRIP-seq:(Medium) rs1430384806 Functional Loss SNV dbSNP153 33..33 33 - - - 91750 RMVar_ID_91750 Human_SNP_ID_646848091 m1A Human chr18 + 48730469 48730469 48730469 GCCCCTGTGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTTCTGCGGT GCCCCTGTGGTGTGAGGGGCTTCCGCGGTGTGTGGGGCTTCCGCGGTGTGAGGGGCTTCTGCGGT A T CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:48730072..48730900 26863196 MeRIP-seq:(Medium) rs1308696862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17130834 RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91751 RMVar_ID_91751 Human_SNP_ID_646848268 m1A Human chr18 + 48730696 48730642 48730696 GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGAGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT _________________________________GGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT TGGTGTGAGGGGCTTCTGCGGTGTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGA T CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730669..48730812 26863196 MeRIP-seq:(Medium) rs1568172128 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91752 RMVar_ID_91752 Human_SNP_ID_646848292 m1A Human chr18 - 48730663 48730663 48730663 CAGGGGCTCCTCACACCGCAGAAGCCCCTCACACCGCAGAAGCCCCTCACACCACAGGGGCCCCT CAGGGGCTCCTCACACCGCAGAAGCCCCTCACGCCGCAGAAGCCCCTCACACCACAGGGGCCCCT T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:48730616..48730736 26863196 MeRIP-seq:(Medium) rs112961253 Functional Loss SNV dbSNP153 33..33 33 - - - 91753 RMVar_ID_91753 Human_SNP_ID_646848307 m1A Human chr18 + 48730696 48730678 48730696 GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGAGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT GTGAGGGGCTTCTGC__________________GGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT CGGTGTGAGGAGCCCCTGA C CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730669..48730812 26863196 MeRIP-seq:(Medium) rs1371118368 Functional Loss DEL dbSNP153 16..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91754 RMVar_ID_91754 Human_SNP_ID_646848332 m1A Human chr18 + 48730696 48730696 48730696 GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGAGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGCGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT A C CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730669..48730812 26863196 MeRIP-seq:(Medium) rs73956012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91755 RMVar_ID_91755 Human_SNP_ID_646848333 m1A Human chr18 + 48730696 48730696 48730696 GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGAGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGTGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT A T CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730669..48730812 26863196 MeRIP-seq:(Medium) rs73956012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 91756 RMVar_ID_91756 Human_SNP_ID_646855503 m1A Human chr18 + 48758108 48758108 48758108 CGGCGCTGGCACCATGGCAACATGAAGCACCCACCAGGCGACAAGGGGGAGGCAGGCGCACACCG CGGCGCTGGCACCATGGCAACATGAAGCACCCGCCAGGCGACAAGGGGGAGGCAGGCGCACACCG A G CTIF Ensembl:ENSG00000134030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:48758059..48758166 26863196 MeRIP-seq:(Medium) rs755607388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_190025,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023,RMVar_hsa_circ_277915,RMVar_hsa_circ_311144,RMVar_hsa_circ_370888,RMVar_hsa_circ_190026,RMVar_hsa_circ_190024 91757 RMVar_ID_91757 Human_SNP_ID_646863232 m1A Human chr18 + 48787306 48787306 48787306 AAGGAAAAGAAAGAAGGGAAGGGGAGGCGGGGAAAGGGAAGGAAGAAAGAAAGACAGAAAGAGAG AAGGAAAAGAAAGAAGGGAAGGGGAGGCGGGGGAAGGGAAGGAAGAAAGAAAGACAGAAAGAGAG A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48787302..48787436 26863196 MeRIP-seq:(Medium) rs957767106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_126697,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_190025,RMVar_hsa_circ_190023,RMVar_hsa_circ_311144,RMVar_hsa_circ_370888,RMVar_hsa_circ_190026,RMVar_hsa_circ_190028,RMVar_hsa_circ_299318 91758 RMVar_ID_91758 Human_SNP_ID_646871180 m1A Human chr18 + 48819962 48819962 48819962 GCATGGAGAGACAGCTAAGTGCACTAGGGACAACGAGGCCGGAGGATGGAAGGAAGTGCCCGGGG GCATGGAGAGACAGCTAAGTGCACTAGGGACACCGAGGCCGGAGGATGGAAGGAAGTGCCCGGGG A C CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48819961..48820068 26863196 MeRIP-seq:(Medium) rs1226037438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126697,RMVar_hsa_circ_190015,RMVar_hsa_circ_370888,RMVar_hsa_circ_190026 91759 RMVar_ID_91759 Human_SNP_ID_646881069 m1A Human chr18 + 48859611 48859611 48859611 GCGGCCCACGGGCAGCTGGGGCCCTGGTGCACAGGGCCAGATGGACAGGCGGGAGGACAGGGGTG GCGGCCCACGGGCAGCTGGGGCCCTGGTGCACGGGGCCAGATGGACAGGCGGGAGGACAGGGGTG A G CTIF Ensembl:ENSG00000134030 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48859561..48859772 26863196 MeRIP-seq:(Medium) rs751236254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9379873,Human_RBP_ID_22064522 91760 RMVar_ID_91760 Human_SNP_ID_646881510 m1A Human chr18 + 48860777 48860777 48860777 CAGCCCTCCGTGAGCTCTTGGGAAAGGGGTGAATTCACTGGGTCATGGAAGGGACAGTCAGGTGA CAGCCCTCCGTGAGCTCTTGGGAAAGGGGTGACTTCACTGGGTCATGGAAGGGACAGTCAGGTGA A C CTIF Ensembl:ENSG00000134030 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:48860728..48860899 26863196 MeRIP-seq:(Medium) rs1244601160 Functional Loss SNV dbSNP153 33..33 33 - - - 91761 RMVar_ID_91761 Human_SNP_ID_646897620 m1A Human chr18 - 48921647 48921647 48921647 GGGAGGTGGATGGTGTGTGGGTGTACAACCGCAGCAGTTACCCCATCTTCATCAAGTCCGCCACA GGGAGGTGGATGGTGTGTGGGTGTACAACCGCTGCAGTTACCCCATCTTCATCAAGTCCGCCACA T A SMAD7 Ensembl:ENSG00000101665 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:48921598..48921848 32194978 MeRIP-seq:(Medium) rs944090062 Functional Loss SNV dbSNP153 33..33 33 - - - 91762 RMVar_ID_91762 Human_SNP_ID_646905979 m1A Human chr18 + 48950315 48950315 48950315 GCGCTCGGCTGTCCGTCGCCCCTTCTCCCCGCAGCTCGCCTCCTCCTCCACCTCCCCCTGCGCCC GCGCTCGGCTGTCCGTCGCCCCTTCTCCCCGCCGCTCGCCTCCTCCTCCACCTCCCCCTGCGCCC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr18:48950230..48950390;chr18:48950093..48950598;chr18:48950126..48950600 26863196 MeRIP-seq:(Medium) rs930431967 Functional Loss SNV dbSNP153 33..33 33 - - - 91763 RMVar_ID_91763 Human_SNP_ID_646906478 m1A Human chr18 + 48951687 48951687 48951687 CCTGGCCGCGGCTGGCCGCCGAGGCTCCCCGCATGGGCTGCTCGCCTCGACCCAGCTGCGGCGGC CCTGGCCGCGGCTGGCCGCCGAGGCTCCCCGCCTGGGCTGCTCGCCTCGACCCAGCTGCGGCGGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48951638..48951890 26863196 MeRIP-seq:(Medium) rs1309505615 Functional Loss SNV dbSNP153 33..33 33 - - - 91764 RMVar_ID_91764 Human_SNP_ID_646906509 m1A Human chr18 - 48951784 48951784 48951784 GAGCGCCAGGAGAGGGCGGACCGGGGACAAGGAGGCTCCCGGGCGCGACGAGGAGAGTCTCGGAG GAGCGCCAGGAGAGGGCGGACCGGGGACAAGGGGGCTCCCGGGCGCGACGAGGAGAGTCTCGGAG T C SMAD7 Ensembl:ENSG00000101665 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:48951443..48951986 26863196 MeRIP-seq:(Medium) rs1201942171 Functional Loss SNV dbSNP153 33..33 33 - - - 91765 RMVar_ID_91765 Human_SNP_ID_646917703 m1A Human chr18 - 48993012 48993011 48993012 TGAAGGTGGATGAGCGTGGCAGTGTGACATTAAGTTAACAGATGGCTGCAGTGGTTTGGTGACAA TGAAGGTGGATGAGCGTGGCAGTGTGACATTA_GTTAACAGATGGCTGCAGTGGTTTGGTGACAA CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48992962..48993040 26863196 MeRIP-seq:(Medium) rs1340549641 Functional Loss DEL dbSNP153 33..33 33 - - - 91766 RMVar_ID_91766 Human_SNP_ID_646917704 m1A Human chr18 - 48993012 48993012 48993012 TGAAGGTGGATGAGCGTGGCAGTGTGACATTAAGTTAACAGATGGCTGCAGTGGTTTGGTGACAA TGAAGGTGGATGAGCGTGGCAGTGTGACATTAGGTTAACAGATGGCTGCAGTGGTTTGGTGACAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48992962..48993040 26863196 MeRIP-seq:(Medium) rs1287374952 Functional Loss SNV dbSNP153 33..33 33 - - - 91767 RMVar_ID_91767 Human_SNP_ID_646920389 m1A Human chr18 - 49003436 49003436 49003436 GGTGGAGTTCAAGGACCAAGTTCCGGGCATCTAACCCAAGAGGGCAGGGAGGAGAGGAAGGAGTC GGTGGAGTTCAAGGACCAAGTTCCGGGCATCTGACCCAAGAGGGCAGGGAGGAGAGGAAGGAGTC T C lnc-DYM-1,lnc-DYM-1:2 RNACentral:URS00008B2A3D,RNACentral:URS00008BDF2C lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:49003407..49003616 26863196 MeRIP-seq:(Medium) rs1253817384 Functional Loss SNV dbSNP153 33..33 33 - - - 91768 RMVar_ID_91768 Human_SNP_ID_646925215 m1A Human chr18 + 49021311 49021311 49021311 GGCCCTGGCTACCCCTCTAGCCCTTCACCAGGACATCCCATCCCCACCTCTCCAGGCAAAGCGCA GGCCCTGGCTACCCCTCTAGCCCTTCACCAGGGCATCCCATCCCCACCTCTCCAGGCAAAGCGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:49021186..49021443 26863196 MeRIP-seq:(Medium) rs746289286 Functional Loss SNV dbSNP153 33..33 33 - - - 91769 RMVar_ID_91769 Human_SNP_ID_646997961 m1A Human chr18 + 49304851 49304851 49304851 TTTGTAAATTTCTACGTCCCTGCAGACAAGGCACCCAACAACACAGCCTCTAAGTCCTTGATCTG TTTGTAAATTTCTACGTCCCTGCAGACAAGGCGCCCAACAACACAGCCTCTAAGTCCTTGATCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:49304849..49305034 26863196 MeRIP-seq:(Medium) rs1047616046 Functional Loss SNV dbSNP153 33..33 33 - - - 91770 RMVar_ID_91770 Human_SNP_ID_647037826 m1A Human chr18 + 49460519 49460519 49460519 GCCGCCGCAGCCCAGGTGGCGCACACCGGCTCAGGCCTCCATGTTTCCACGTCTCAGCGGGTACA GCCGCCGCAGCCCAGGTGGCGCACACCGGCTCCGGCCTCCATGTTTCCACGTCTCAGCGGGTACA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:49460471..49460676 26863196 MeRIP-seq:(Medium) rs1305022554 Functional Loss SNV dbSNP153 33..33 33 - - - 91771 RMVar_ID_91771 Human_SNP_ID_647037829 m1A Human chr18 + 49460535 49460535 49460535 TGGCGCACACCGGCTCAGGCCTCCATGTTTCCACGTCTCAGCGGGTACAGATCCGGCTCCGGTCC TGGCGCACACCGGCTCAGGCCTCCATGTTTCCGCGTCTCAGCGGGTACAGATCCGGCTCCGGTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:49460485..49460630 26863196 MeRIP-seq:(Medium) rs1288169460 Functional Loss SNV dbSNP153 33..33 33 - - - 91772 RMVar_ID_91772 Human_SNP_ID_647043233 m1A Human chr18 + 49481928 49481928 49481928 TACCTCCCAAAATTCTACCTTCATTTCCCTGCACAGTTTCACTGGACTGTTTCACAACAAAATTG TACCTCCCAAAATTCTACCTTCATTTCCCTGCGCAGTTTCACTGGACTGTTTCACAACAAAATTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:49481877..49482026 32194978 MeRIP-seq:(Medium) rs909196242 Functional Loss SNV dbSNP153 33..33 33 - - - 91773 RMVar_ID_91773 Human_SNP_ID_647044921 m1A Human chr18 - 49487150 49487150 49487150 TGGGTTGGGCTTTGTAGCTGCTCCGCAGGCCCAGCCCGGGCCGCGCTCGCAGAGTCCTAGGCGGT TGGGTTGGGCTTTGTAGCTGCTCCGCAGGCCCGGCCCGGGCCGCGCTCGCAGAGTCCTAGGCGGT T C C18orf32,RPL17-C18orf32 Ensembl:ENSG00000177576,Ensembl:ENSG00000215472 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:49487103..49487197;chr18:49487101..49487196 26863196 MeRIP-seq:(Medium) rs1435012308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4488344,Human_RBP_ID_18420730,Human_RBP_ID_26759316 Human_miRNA_ID_1158080 91774 RMVar_ID_91774 Human_SNP_ID_647044938 m1A Human chr18 + 49487178 49487178 49487178 GGGCTGGGCCTGCGGAGCAGCTACAAAGCCCAACCCAGGCCGCTAGCCCGGGCACACTCACCCGC GGGCTGGGCCTGCGGAGCAGCTACAAAGCCCAGCCCAGGCCGCTAGCCCGGGCACACTCACCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:49487092..49487191 26863196 MeRIP-seq:(Medium) rs1385518212 Functional Loss SNV dbSNP153 33..33 33 - - - 91775 RMVar_ID_91775 Human_SNP_ID_647046077 m1A Human chr18 - 49490548 49490548 49490548 ATGACTCATCATCTCCATTTTCTTTCAGGCCAAGCAATGGGGCTGGACACAAGGTCGGTGGCCCA ATGACTCATCATCTCCATTTTCTTTCAGGCCAGGCAATGGGGCTGGACACAAGGTCGGTGGCCCA T C RPL17,RPL17-C18orf32 Ensembl:ENSG00000265681,Ensembl:ENSG00000215472 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:49490530..49490603 26863196 MeRIP-seq:(Medium) rs770958670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_201839,Human_RBP_ID_238681,Human_RBP_ID_509102,Human_RBP_ID_769202,Human_RBP_ID_823203,Human_RBP_ID_906356,Human_RBP_ID_1550316,Human_RBP_ID_1876314,Human_RBP_ID_8472289,Human_RBP_ID_9081434,Human_RBP_ID_9379614,Human_RBP_ID_17265350,Human_RBP_ID_17381622,Human_RBP_ID_17497572,Human_RBP_ID_17913459,Human_RBP_ID_18717759,Human_RBP_ID_22590125,Human_RBP_ID_22661020,Human_RBP_ID_23210651,Human_RBP_ID_25366264,Human_RBP_ID_26334414 Human_Splice_Rec_1911624,Human_Splice_Rec_1911625,Human_Splice_Rec_1911636,Human_Splice_Rec_1911637,Human_Splice_Rec_1911648,Human_Splice_Rec_1911649,Human_Splice_Rec_1911668,Human_Splice_Rec_1911669,Human_Splice_Rec_1911674,Human_Splice_Rec_1911675,Human_Splice_Rec_1911688,Human_Splice_Rec_1911689,Human_Splice_Rec_1911698,Human_Splice_Rec_1911699,Human_Splice_Rec_1911710,Human_Splice_Rec_1911711,Human_Splice_Rec_1911720,Human_Splice_Rec_1911721,Human_Splice_Rec_1911732,Human_Splice_Rec_1911733,Human_Splice_Rec_1911742,Human_Splice_Rec_1911743,Human_Splice_Rec_1911756,Human_Splice_Rec_1911757,Human_Splice_Rec_1911768,Human_Splice_Rec_1911769,Human_Splice_Rec_1911773,Human_Splice_Rec_1911782,Human_Splice_Rec_1911783,Human_Splice_Rec_1911790,Human_Splice_Rec_1911791,Human_Splice_Rec_1911793,Human_Splice_Rec_1911804,Human_Splice_Rec_1911805,Human_Splice_Rec_1911816,Human_Splice_Rec_1911817,Human_Splice_Rec_1911826,Human_Splice_Rec_1911827,Human_Splice_Rec_1911830,Human_Splice_Rec_1911838 Human_miRNA_ID_2930391,Human_miRNA_ID_2930392,Human_miRNA_ID_2930393,Human_miRNA_ID_2974890,Human_miRNA_ID_2974891,Human_miRNA_ID_2974892,Human_miRNA_ID_3008087,Human_miRNA_ID_3008088,Human_miRNA_ID_3008089 RMVar_hsa_circ_96322,RMVar_hsa_circ_118761,RMVar_hsa_circ_190081,RMVar_hsa_circ_112901,RMVar_hsa_circ_190083,RMVar_hsa_circ_95539,RMVar_hsa_circ_113275,RMVar_hsa_circ_190084,RMVar_hsa_circ_190085,RMVar_hsa_circ_190086 91776 RMVar_ID_91776 Human_SNP_ID_647046496 m1A Human chr18 + 49491732 49491732 49491732 AAGGTGTCCTAAGAAATGCCATCATCGCAGCCATACTTTCCCCCACCAAGGGCTTGCTTTCCCTT AAGGTGTCCTAAGAAATGCCATCATCGCAGCCTTACTTTCCCCCACCAAGGGCTTGCTTTCCCTT A T AC100778.3 Ensembl:ENSG00000265496 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:49491701..49492473 26863196 MeRIP-seq:(Medium) rs1370191476 Functional Loss SNV dbSNP153 33..33 33 - - - 91777 RMVar_ID_91777 Human_SNP_ID_647046511 m1A Human chr18 - 49491753 49491753 49491753 GCTGTAGTTACTGGAAGATAAAAGGGAAAGCAAGCCCTTGGTGGGGGAAAGTATGGCTGCGATGA GCTGTAGTTACTGGAAGATAAAAGGGAAAGCAGGCCCTTGGTGGGGGAAAGTATGGCTGCGATGA T C RPL17,RPL17-C18orf32 Ensembl:ENSG00000265681,Ensembl:ENSG00000215472 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:49491751..49492500 26863196 MeRIP-seq:(Medium) rs1289425094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_509113,Human_RBP_ID_1550336,Human_RBP_ID_1876329,Human_RBP_ID_3556955,Human_RBP_ID_4494601,Human_RBP_ID_6691568,Human_RBP_ID_8472302,Human_RBP_ID_17266069,Human_RBP_ID_18717780,Human_RBP_ID_22501226,Human_RBP_ID_22589582,Human_RBP_ID_22808544,Human_RBP_ID_22965949,Human_RBP_ID_23210657,Human_RBP_ID_23772373,Human_RBP_ID_25378974 Human_Splice_Rec_1911660,Human_Splice_Rec_1911661,Human_Splice_Rec_1911680,Human_Splice_Rec_1911681,Human_Splice_Rec_1911748,Human_Splice_Rec_1911749,Human_Splice_Rec_1911776,Human_Splice_Rec_1911796,Human_Splice_Rec_1911797,Human_Splice_Rec_1911808,Human_Splice_Rec_1911809,Human_Splice_Rec_1911820,Human_Splice_Rec_1911832,Human_Splice_Rec_1911854 RMVar_hsa_circ_101906,RMVar_hsa_circ_190088,RMVar_hsa_circ_190090,RMVar_hsa_circ_377384 91778 RMVar_ID_91778 Human_SNP_ID_647046647 m1A Human chr18 - 49492115 49492115 49492115 AGGTCCGGTGTCTAGTGGTGAGTGGTGGCCGCAACGAGGAAAAAGTTTTGGGGGAAAGAAAAGTC AGGTCCGGTGTCTAGTGGTGAGTGGTGGCCGCCACGAGGAAAAAGTTTTGGGGGAAAGAAAAGTC T G RPL17,RPL17-C18orf32 Ensembl:ENSG00000265681,Ensembl:ENSG00000215472 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:49492106..49492410 26863196 MeRIP-seq:(Medium) rs1175860199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23772389,Human_RBP_ID_25366322 RMVar_hsa_circ_101906,RMVar_hsa_circ_190088 91779 RMVar_ID_91779 Human_SNP_ID_647046673 m1A Human chr18 + 49492179 49492179 49492179 TCCGGAGTCCGCACGGACCCCAGGCGGCCCGCACCCCACGGCGGGCCGGCGCCCCCACCAGTGGA TCCGGAGTCCGCACGGACCCCAGGCGGCCCGCCCCCCACGGCGGGCCGGCGCCCCCACCAGTGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:49492170..49492270 32194978 MeRIP-seq:(Medium) rs1004231534 Functional Loss SNV dbSNP153 33..33 33 - - - 91780 RMVar_ID_91780 Human_SNP_ID_647121659 m1A Human chr18 - 49783727 49783727 49783727 CTGGCCATGCCCTGCCATTGAAACAGTGATTAAGTTTGATCAAGCCATGGTGACACAAAAATGCA CTGGCCATGCCCTGCCATTGAAACAGTGATTACGTTTGATCAAGCCATGGTGACACAAAAATGCA T G ACAA2 Ensembl:ENSG00000167315 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:49783657..49783907 32194978 MeRIP-seq:(Medium) rs1056313875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_509130,Human_RBP_ID_1876336,Human_RBP_ID_23210659,Human_RBP_ID_23772400 91781 RMVar_ID_91781 Human_SNP_ID_647124163 m1A Human chr18 - 49792243 49792243 49792243 AAAGAAAGGAAAACAGACAATGCAGGTAGACGAGCATGCTCGGCCCCAAACCACCCTGGAACAGT AAAGAAAGGAAAACAGACAATGCAGGTAGACGGGCATGCTCGGCCCCAAACCACCCTGGAACAGT T C ACAA2 Ensembl:ENSG00000167315 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:49791591..49792243 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_509133,Human_RBP_ID_6691635 Human_Splice_Rec_1911928,Human_Splice_Rec_1911929,Human_Splice_Rec_1911946,Human_Splice_Rec_1911947,Human_Splice_Rec_1911966,Human_Splice_Rec_1911967 RMVar_hsa_circ_190097,RMVar_hsa_circ_112841,RMVar_hsa_circ_57241,RMVar_hsa_circ_365357,RMVar_hsa_circ_64788 91782 RMVar_ID_91782 Human_SNP_ID_647130543 m1A Human chr18 - 49814180 49814180 49814180 CGGCGCCGCCCGCAATGGGACCTGATCATATAAGGAAAATACTGCGGGCTCATCCGGGGGCTGCA CGGCGCCGCCCGCAATGGGACCTGATCATATAGGGAAAATACTGCGGGCTCATCCGGGGGCTGCA T C AC090227.2 Ensembl:ENSG00000266997 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:49814072..49814372 32194978 MeRIP-seq:(Medium) rs962162383 Functional Loss SNV dbSNP153 33..33 33 - - - 91783 RMVar_ID_91783 Human_SNP_ID_647130544 m1A Human chr18 - 49814180 49814180 49814180 CGGCGCCGCCCGCAATGGGACCTGATCATATAAGGAAAATACTGCGGGCTCATCCGGGGGCTGCA CGGCGCCGCCCGCAATGGGACCTGATCATATACGGAAAATACTGCGGGCTCATCCGGGGGCTGCA T G AC090227.2 Ensembl:ENSG00000266997 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:49814072..49814372 32194978 MeRIP-seq:(Medium) rs962162383 Functional Loss SNV dbSNP153 33..33 33 - - - 91784 RMVar_ID_91784 Human_SNP_ID_647130597 m1A Human chr18 + 49814278 49814278 49814278 GGCGAGCGAAATGGGGCCAGGGGACCTGGAGCAGGGGCGTGAGGAGAGTAGGCAGCGGGTGAGGC GGCGAGCGAAATGGGGCCAGGGGACCTGGAGCGGGGGCGTGAGGAGAGTAGGCAGCGGGTGAGGC A G SNHG22 Ensembl:ENSG00000267322 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:49814001..49814450 26863196 MeRIP-seq:(Medium) rs11549021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238842,Human_RBP_ID_509142,Human_RBP_ID_823154,Human_RBP_ID_1064008,Human_RBP_ID_1093224,Human_RBP_ID_2544319,Human_RBP_ID_5088669,Human_RBP_ID_5291838,Human_RBP_ID_5584647,Human_RBP_ID_6691656,Human_RBP_ID_8255499,Human_RBP_ID_8827468,Human_RBP_ID_9424853,Human_RBP_ID_13319740,Human_RBP_ID_17068233,Human_RBP_ID_18944071,Human_RBP_ID_20346895,Human_RBP_ID_22533028,Human_RBP_ID_22741246,Human_RBP_ID_23772427,Human_RBP_ID_26979935,Human_RBP_ID_27672686 RMVar_hsa_circ_190099,RMVar_hsa_circ_190098 91785 RMVar_ID_91785 Human_SNP_ID_647165546 m1A Human chr18 - 49944794 49944794 49944794 GCTCGAGGTGATCGATGGTAAAGTGAGAAGAGAGACAGGCTGAACAGGGAGGGGTTTGAAGCAAC GCTCGAGGTGATCGATGGTAAAGTGAGAAGAGGGACAGGCTGAACAGGGAGGGGTTTGAAGCAAC T C MYO5B Ensembl:ENSG00000167306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:49944792..49944980 26863196 MeRIP-seq:(Medium) rs984215935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52329,RMVar_hsa_circ_190111,RMVar_hsa_circ_190107,RMVar_hsa_circ_317498,RMVar_hsa_circ_320311,RMVar_hsa_circ_88493,RMVar_hsa_circ_190109,RMVar_hsa_circ_190110,RMVar_hsa_circ_307951,RMVar_hsa_circ_288224,RMVar_hsa_circ_190113 91786 RMVar_ID_91786 Human_SNP_ID_647169383 m1A Human chr18 + 49957939 49957939 49957939 TTGCCATCACAGAAGCCCAGCTGGCCCCCCCCAGGACTCTGCAGTCCTCACTGCTCTCTAGAATG TTGCCATCACAGAAGCCCAGCTGGCCCCCCCCGGGACTCTGCAGTCCTCACTGCTCTCTAGAATG A G HSALNG0121510 RNACentral:URS0000EA4EB9 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:49957928..49957993 26863196 MeRIP-seq:(Medium) rs899736022 Functional Loss SNV dbSNP153 33..33 33 - - - 91787 RMVar_ID_91787 Human_SNP_ID_647179131 m1A Human chr18 - 49993931 49993931 49993931 AGCCGGGACCAAGGGCAAGATTAGAGGCAGGGAAGGGTCGGTTCCTGCCAAGCACATAAGCCATG AGCCGGGACCAAGGGCAAGATTAGAGGCAGGGGAGGGTCGGTTCCTGCCAAGCACATAAGCCATG T C MYO5B Ensembl:ENSG00000167306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:49993929..49994066 26863196 MeRIP-seq:(Medium) rs946122124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190111,RMVar_hsa_circ_88493,RMVar_hsa_circ_71396,RMVar_hsa_circ_339237,RMVar_hsa_circ_190118,RMVar_hsa_circ_190117 91788 RMVar_ID_91788 Human_SNP_ID_647209457 m1A Human chr18 + 50106003 50106003 50106003 AGTCACCCTCTCCAGCTACTTTTTATAGAACCACCTCAAATTCATACTATTCAAGCCATAACTCA AGTCACCCTCTCCAGCTACTTTTTATAGAACCCCCTCAAATTCATACTATTCAAGCCATAACTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:50106001..50106251 26863196 MeRIP-seq:(Medium) rs992784480 Functional Loss SNV dbSNP153 33..33 33 - - - 91789 RMVar_ID_91789 Human_SNP_ID_647220423 m1A Human chr18 + 50147389 50147389 50147389 CTGCCACTGCCCTGTCCACAGTCACCTGAATTACTGCAGTGACCTCCTGATTAGCACCCCTTCTT CTGCCACTGCCCTGTCCACAGTCACCTGAATTTCTGCAGTGACCTCCTGATTAGCACCCCTTCTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50147381..50147471 26863196 MeRIP-seq:(Medium) rs1222328382 Functional Loss SNV dbSNP153 33..33 33 - - - 91790 RMVar_ID_91790 Human_SNP_ID_647232171 m1A Human chr18 - 50193940 50193940 50193940 GAGGCTGGGTGCTCCGAATCGGGAACAGGTGCAGCCCGGGCGGAGACGCCCGCGTTCCGCAGCAG GAGGCTGGGTGCTCCGAATCGGGAACAGGTGCCGCCCGGGCGGAGACGCCCGCGTTCCGCAGCAG T G MYO5B Ensembl:ENSG00000167306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50193934..50194126 26863196 MeRIP-seq:(Medium) rs1013958344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561213 91791 RMVar_ID_91791 Human_SNP_ID_647243132 m1A Human chr18 - 50238707 50238707 50238707 TCATTTGACATATAATTACTTTTGCTTTTCTTAGTGCAACGAGAAGCTAAAGAACAGGAAGAACG TCATTTGACATATAATTACTTTTGCTTTTCTTGGTGCAACGAGAAGCTAAAGAACAGGAAGAACG T C CFAP53 Ensembl:ENSG00000172361 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:50238681..50238765 26863196 MeRIP-seq:(Medium) rs1246328883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13897 91792 RMVar_ID_91792 Human_SNP_ID_647252825 m1A Human chr18 - 50275197 50275197 50275197 GCAAGGGAGGCTGTGACTCCAAGATGGCTGCCAGGCGGCGCCCCGGAGCCCAGCCACTGCCTCCA GCAAGGGAGGCTGTGACTCCAAGATGGCTGCCGGGCGGCGCCCCGGAGCCCAGCCACTGCCTCCA T C MBD1 Ensembl:ENSG00000141644 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50275065..50275204 26863196 MeRIP-seq:(Medium) rs763620378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1912178,Human_Splice_Rec_1912179,Human_Splice_Rec_1912202,Human_Splice_Rec_1912203,Human_Splice_Rec_1912228,Human_Splice_Rec_1912229,Human_Splice_Rec_1912258,Human_Splice_Rec_1912259,Human_Splice_Rec_1912290,Human_Splice_Rec_1912291,Human_Splice_Rec_1912320,Human_Splice_Rec_1912321,Human_Splice_Rec_1912346,Human_Splice_Rec_1912347,Human_Splice_Rec_1912378,Human_Splice_Rec_1912379,Human_Splice_Rec_1912404,Human_Splice_Rec_1912405,Human_Splice_Rec_1912434,Human_Splice_Rec_1912435,Human_Splice_Rec_1912464,Human_Splice_Rec_1912465,Human_Splice_Rec_1912488,Human_Splice_Rec_1912489,Human_Splice_Rec_1912516,Human_Splice_Rec_1912517,Human_Splice_Rec_1912533,Human_Splice_Rec_1912562,Human_Splice_Rec_1912563,Human_Splice_Rec_1912590,Human_Splice_Rec_1912591,Human_Splice_Rec_1912620,Human_Splice_Rec_1912621,Human_Splice_Rec_1912646,Human_Splice_Rec_1912647,Human_Splice_Rec_1912670,Human_Splice_Rec_1912671,Human_Splice_Rec_1912690,Human_Splice_Rec_1912691,Human_Splice_Rec_1912694,Human_Splice_Rec_1912698 RMVar_hsa_circ_115568,RMVar_hsa_circ_190125 91793 RMVar_ID_91793 Human_SNP_ID_647252830 m1A Human chr18 + 50275243 50275222 50275243 GAGTCACAGCCTCCCTTGCGGCGGGCATGTTTACCCTGGGAAAGATCAGAAAGGGTGGTTTCAGC GAGTCACAGCCT_____________________CCCTGGGAAAGATCAGAAAGGGTGGTTTCAGC TCCCTTGCGGCGGGCATGTTTA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:50275195..50275874 32194978 MeRIP-seq:(Medium) rs1451418069 Functional Loss DEL dbSNP153 13..33 33 - - - 91794 RMVar_ID_91794 Human_SNP_ID_647253422 m1A Human chr18 - 50276895 50276895 50276895 GGTTGGACCCCAGAGTGGTGAGGTCAGGAAGGAGGCCCCGAGGGATGAGACCAAGGCTGACACTG GGTTGGACCCCAGAGTGGTGAGGTCAGGAAGGCGGCCCCGAGGGATGAGACCAAGGCTGACACTG T G MBD1 Ensembl:ENSG00000141644 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:50276743..50276894 32194978 MeRIP-seq:(Medium) rs140046193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905942,Human_RBP_ID_3953805,Human_RBP_ID_18717895,Human_RBP_ID_18993419,Human_RBP_ID_24545317,Human_RBP_ID_26334237,Human_RBP_ID_27814590 Human_Splice_Rec_1912171,Human_Splice_Rec_1912193,Human_Splice_Rec_1912219,Human_Splice_Rec_1912251,Human_Splice_Rec_1912281,Human_Splice_Rec_1912311,Human_Splice_Rec_1912337,Human_Splice_Rec_1912369,Human_Splice_Rec_1912395,Human_Splice_Rec_1912425,Human_Splice_Rec_1912455,Human_Splice_Rec_1912479,Human_Splice_Rec_1912505,Human_Splice_Rec_1912551,Human_Splice_Rec_1912579,Human_Splice_Rec_1912611,Human_Splice_Rec_1912637,Human_Splice_Rec_1912661,Human_Splice_Rec_1912723 RMVar_hsa_circ_115568,RMVar_hsa_circ_190125 91795 RMVar_ID_91795 Human_SNP_ID_647253516 m1A Human chr18 - 50277183 50277183 50277183 CCCATCCCTAGCCCCACAGGAGACAGGATCCGAAGCAAAGTTGAGCTGACTCGATACCTGGGCCC CCCATCCCTAGCCCCACAGGAGACAGGATCCGCAGCAAAGTTGAGCTGACTCGATACCTGGGCCC T G MBD1 Ensembl:ENSG00000141644 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:50277133..50279775 26863196 MeRIP-seq:(Medium) rs113452608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_509177,Human_RBP_ID_823276,Human_RBP_ID_1550417,Human_RBP_ID_13319896,Human_RBP_ID_21891287 Human_Splice_Rec_1912168,Human_Splice_Rec_1912169,Human_Splice_Rec_1912216,Human_Splice_Rec_1912217,Human_Splice_Rec_1912248,Human_Splice_Rec_1912249,Human_Splice_Rec_1912278,Human_Splice_Rec_1912279,Human_Splice_Rec_1912308,Human_Splice_Rec_1912309,Human_Splice_Rec_1912334,Human_Splice_Rec_1912335,Human_Splice_Rec_1912366,Human_Splice_Rec_1912367,Human_Splice_Rec_1912392,Human_Splice_Rec_1912393,Human_Splice_Rec_1912422,Human_Splice_Rec_1912423,Human_Splice_Rec_1912452,Human_Splice_Rec_1912453,Human_Splice_Rec_1912476,Human_Splice_Rec_1912477,Human_Splice_Rec_1912502,Human_Splice_Rec_1912503,Human_Splice_Rec_1912548,Human_Splice_Rec_1912549,Human_Splice_Rec_1912576,Human_Splice_Rec_1912577,Human_Splice_Rec_1912608,Human_Splice_Rec_1912609,Human_Splice_Rec_1912634,Human_Splice_Rec_1912635,Human_Splice_Rec_1912658,Human_Splice_Rec_1912659,Human_Splice_Rec_1912702,Human_Splice_Rec_1912703,Human_Splice_Rec_1912714,Human_Splice_Rec_1912715,Human_Splice_Rec_1912720,Human_Splice_Rec_1912721 RMVar_hsa_circ_115568,RMVar_hsa_circ_190125 91796 RMVar_ID_91796 Human_SNP_ID_647254271 m1A Human chr18 + 50279995 50279995 50279995 GGCCGGGCAGTCCAGCCAGTCCTCAGCCATGGAGGCCACAGGAAGCAGCAGTAGCCTGAAAGGGG GGCCGGGCAGTCCAGCCAGTCCTCAGCCATGGCGGCCACAGGAAGCAGCAGTAGCCTGAAAGGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50279946..50280042 26863196 MeRIP-seq:(Medium) rs776932693 Functional Loss SNV dbSNP153 33..33 33 - - - 91797 RMVar_ID_91797 Human_SNP_ID_647254672 m1A Human chr18 - 50281426 50281426 50281426 GAAGGGGAGGAGGGCGAGGCGGGAGGTGCAGGAGGGACCCTCGCCATGGGTCCACGGGCCTAGAG GAAGGGGAGGAGGGCGAGGCGGGAGGTGCAGGGGGGACCCTCGCCATGGGTCCACGGGCCTAGAG T C MBD1 Ensembl:ENSG00000141644 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:50281338..50281525;chr18:50279868..50281674;chr18:50279862..50281575;chr18:50281320..50281624 26863196 MeRIP-seq:(Medium) rs921428810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238636,Human_RBP_ID_769102,Human_RBP_ID_905943,Human_RBP_ID_3953596,Human_RBP_ID_4494023,Human_RBP_ID_5368946,Human_RBP_ID_5526596,Human_RBP_ID_9424740,Human_RBP_ID_18420672,Human_RBP_ID_18993423,Human_RBP_ID_22965726,Human_RBP_ID_23210733,Human_RBP_ID_26334424,Human_RBP_ID_27814592 Human_Splice_Rec_1912165,Human_Splice_Rec_1912213,Human_Splice_Rec_1912245,Human_Splice_Rec_1912275,Human_Splice_Rec_1912305,Human_Splice_Rec_1912331,Human_Splice_Rec_1912363,Human_Splice_Rec_1912389,Human_Splice_Rec_1912419,Human_Splice_Rec_1912573,Human_Splice_Rec_1912605,Human_Splice_Rec_1912699,Human_Splice_Rec_1912711,Human_Splice_Rec_1912717,Human_Splice_Rec_1912725 RMVar_hsa_circ_115568,RMVar_hsa_circ_190125 91798 RMVar_ID_91798 Human_SNP_ID_647255403 m1A Human chr18 - 50283319 50283319 50283319 CTCTTCTGTGATGTGTATAATCCTCAGAGCAAAACATACTGTAAGCGGCTCCAGGTGCTGTGCCC CTCTTCTGTGATGTGTATAATCCTCAGAGCAAGACATACTGTAAGCGGCTCCAGGTGCTGTGCCC T C CXXC1 Ensembl:ENSG00000154832 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:50283250..50283400 32194978 MeRIP-seq:(Medium) rs754605356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1876407,Human_RBP_ID_9379880,Human_RBP_ID_18717916 Human_Splice_Rec_1912750,Human_Splice_Rec_1912751,Human_Splice_Rec_1912778,Human_Splice_Rec_1912779,Human_Splice_Rec_1912806,Human_Splice_Rec_1912807,Human_Splice_Rec_1912830,Human_Splice_Rec_1912831,Human_Splice_Rec_1912856,Human_Splice_Rec_1912857,Human_Splice_Rec_1912882,Human_Splice_Rec_1912883,Human_Splice_Rec_1912889,Human_Splice_Rec_1912894,Human_Splice_Rec_1912895,Human_Splice_Rec_1912900 Human_miRNA_ID_2067836 RMVar_hsa_circ_190127,RMVar_hsa_circ_119529 91799 RMVar_ID_91799 Human_SNP_ID_647255847 m1A Human chr18 - 50284540 50284540 50284540 TGCTCAACAGAAGGAGGAGCGATACAAGCGGCATCGGCAGAAGCAGAAGCACAAGGATAAATGGA TGCTCAACAGAAGGAGGAGCGATACAAGCGGCGTCGGCAGAAGCAGAAGCACAAGGATAAATGGA T C CXXC1 Ensembl:ENSG00000154832 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:50284491..50284575 26863196 MeRIP-seq:(Medium) rs761614989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51862,Human_RBP_ID_238653,Human_RBP_ID_905945,Human_RBP_ID_9379629,Human_RBP_ID_18993428,Human_RBP_ID_22661037,Human_RBP_ID_24545319,Human_RBP_ID_26334428,Human_RBP_ID_27814598 Human_Splice_Rec_1912742,Human_Splice_Rec_1912770,Human_Splice_Rec_1912798,Human_Splice_Rec_1912822,Human_Splice_Rec_1912848,Human_Splice_Rec_1912874,Human_Splice_Rec_1912904,Human_Splice_Rec_1912914,Human_Splice_Rec_1912924,Human_Splice_Rec_1912928 RMVar_hsa_circ_190127,RMVar_hsa_circ_119529 91800 RMVar_ID_91800 Human_SNP_ID_647255936 m1A Human chr18 + 50284741 50284741 50284741 ATCCACTTTACCCTCTCCATCACCTTCTTCTCAGACTTCTTCTCCCGACGCTTCACATGCTTCAC ATCCACTTTACCCTCTCCATCACCTTCTTCTCGGACTTCTTCTCCCGACGCTTCACATGCTTCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:50284723..50284850 26863196 MeRIP-seq:(Medium) rs775859432 Functional Loss SNV dbSNP153 33..33 33 - - - 91801 RMVar_ID_91801 Human_SNP_ID_647256230 m1A Human chr18 - 50285470 50285470 50285470 TACAGATCAGGCAGGGCTGAGCATTCCTGGCAATGAGGGGTAGCGGGGAGGTGTGTCTGGGGAGG TACAGATCAGGCAGGGCTGAGCATTCCTGGCAGTGAGGGGTAGCGGGGAGGTGTGTCTGGGGAGG T C CXXC1 Ensembl:ENSG00000154832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50285420..50285537 26863196 MeRIP-seq:(Medium) rs921890548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262921,Human_RBP_ID_3953597,Human_RBP_ID_13319906,Human_RBP_ID_18412150,Human_RBP_ID_21976861,Human_RBP_ID_22476126,Human_RBP_ID_25376913,Human_RBP_ID_27838938 RMVar_hsa_circ_95488,RMVar_hsa_circ_100072,RMVar_hsa_circ_190127,RMVar_hsa_circ_119529,RMVar_hsa_circ_190129,RMVar_hsa_circ_190130 91802 RMVar_ID_91802 Human_SNP_ID_647256328 m1A Human chr18 + 50285827 50285827 50285827 TTGTTGGGGCCCCCGAACTTCTTCATGTCCCGACAGAAATCACAGTGACCACAGTCCTCAGTGCG TTGTTGGGGCCCCCGAACTTCTTCATGTCCCGGCAGAAATCACAGTGACCACAGTCCTCAGTGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50285707..50285853 26863196 MeRIP-seq:(Medium) rs1314685383 Functional Loss SNV dbSNP153 33..33 33 - - - 91803 RMVar_ID_91803 Human_SNP_ID_647256498 m1A Human chr18 - 50286203 50286203 50286203 TCGCTATCGGCACAAGAAGTCACGGGAGCGGGATGGCAATGAGCGGGACAGCAGTGAGCCCCGGG TCGCTATCGGCACAAGAAGTCACGGGAGCGGGTTGGCAATGAGCGGGACAGCAGTGAGCCCCGGG T A CXXC1 Ensembl:ENSG00000154832 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50286157..50286258 26863196 MeRIP-seq:(Medium) rs754533658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905711,Human_RBP_ID_5583197,Human_RBP_ID_17910462,Human_RBP_ID_18993431,Human_RBP_ID_26334689 Human_Splice_Rec_1912732,Human_Splice_Rec_1912760,Human_Splice_Rec_1912788,Human_Splice_Rec_1912814,Human_Splice_Rec_1912840,Human_Splice_Rec_1912866,Human_Splice_Rec_1912934,Human_Splice_Rec_1912946,Human_Splice_Rec_1912954 RMVar_hsa_circ_190127,RMVar_hsa_circ_119529,RMVar_hsa_circ_311673 91804 RMVar_ID_91804 Human_SNP_ID_647256751 m1A Human chr18 + 50286846 50286846 50286846 GTCCTCCCCGGCATCTGGAGGCTCTGGGTCTGAACCATCTCCCTCCTGCAGGACACCCCCATTAC GTCCTCCCCGGCATCTGGAGGCTCTGGGTCTGGACCATCTCCCTCCTGCAGGACACCCCCATTAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:50286795..50286924 26863196 MeRIP-seq:(Medium) rs138590776 Functional Loss SNV dbSNP153 33..33 33 - - - 91805 RMVar_ID_91805 Human_SNP_ID_647282447 m1A Human chr18 + 50392269 50392269 50392269 TTATAACCTGAGTCCCTTGTGAACTTTTGAACATACCAACAGGGTATAGAGTATAGAGGCTATTT TTATAACCTGAGTCCCTTGTGAACTTTTGAACCTACCAACAGGGTATAGAGTATAGAGGCTATTT A C SKA1 Ensembl:ENSG00000154839 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10460085 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6691999,Human_RBP_ID_13320054,Human_RBP_ID_26463769 GWAS_ID_11862,GWAS_ID_11863,GWAS_ID_11864,GWAS_ID_11865,GWAS_ID_11866 RMVar_hsa_circ_84889,RMVar_hsa_circ_118795,RMVar_hsa_circ_190132,RMVar_hsa_circ_82060,RMVar_hsa_circ_190133,RMVar_hsa_circ_190134 91806 RMVar_ID_91806 Human_SNP_ID_647328216 m1A Human chr18 + 50578959 50578959 50578959 GTGGGGCAGTATCCCTGGAGCAGCATGGGCAGAGGTGAGAGAGAACATGAGTAAGCCTCGCATGG GTGGGGCAGTATCCCTGGAGCAGCATGGGCAGGGGTGAGAGAGAACATGAGTAAGCCTCGCATGG A G MAPK4 Ensembl:ENSG00000141639 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50578954..50579209 26863196 MeRIP-seq:(Medium) rs73430658 Functional Loss SNV dbSNP153 33..33 33 - - - 91807 RMVar_ID_91807 Human_SNP_ID_647342870 m1A Human chr18 + 50645065 50645065 50645065 TGAGGGAGAGCAGAAGGAGAGGCCTGCAGGCCAGGGAGTGGGTGGCTGGGAGAGAGTGGCAGGGA TGAGGGAGAGCAGAAGGAGAGGCCTGCAGGCCCGGGAGTGGGTGGCTGGGAGAGAGTGGCAGGGA A C MAPK4 Ensembl:ENSG00000141639 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50645061..50645144 26863196 MeRIP-seq:(Medium) rs1389016603 Functional Loss SNV dbSNP153 33..33 33 - - - 91808 RMVar_ID_91808 Human_SNP_ID_647362068 m1A Human chr18 - 50729651 50729651 50729651 GCCGTCCACCGGGGCCGGGCGGCCGGGGGGCGAGGCAGACAAGCGGCGCTCGGGGTCGTCGGCGG GCCGTCCACCGGGGCCGGGCGGCCGGGGGGCGCGGCAGACAAGCGGCGCTCGGGGTCGTCGGCGG T G HSALNG0121540 RNACentral:URS0000EAFFBB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50729609..50729717 26863196 MeRIP-seq:(Medium) rs750446711 Functional Loss SNV dbSNP153 33..33 33 - - - 91809 RMVar_ID_91809 Human_SNP_ID_647362117 m1A Human chr18 + 50729717 50729717 50729717 GCGCCAGCCCCCAGTTCGACCTGGACGTGTTCATCTCCCGCGCCCTGAAGCTCTGCACCAAGCCC GCGCCAGCCCCCAGTTCGACCTGGACGTGTTCCTCTCCCGCGCCCTGAAGCTCTGCACCAAGCCC A C MAPK4 Ensembl:ENSG00000141639 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:50729630..50729724 26863410 MeRIP-seq:(Medium) rs748855629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27461569 91810 RMVar_ID_91810 Human_SNP_ID_647362166 m1A Human chr18 + 50729814 50729814 50729814 CAATGGTGCGTGCATCCCCGAGCACCCTGGCGACCTCGTGCAGACCGAGGCCTTCTCCAAAGAAA CAATGGTGCGTGCATCCCCGAGCACCCTGGCGTCCTCGTGCAGACCGAGGCCTTCTCCAAAGAAA A T MAPK4 Ensembl:ENSG00000141639 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:50729801..50729825 26863196 MeRIP-seq:(Medium) rs747847970 Functional Loss SNV dbSNP153 33..33 33 - - - 91811 RMVar_ID_91811 Human_SNP_ID_647400064 m1A Human chr18 + 50879302 50879302 50879302 TCCGCCGGGTGTACCACCTGTCGCGGCGCGAGACCTCTGGTAAGGCCCGGCGCGGTGGGGCCCGG TCCGCCGGGTGTACCACCTGTCGCGGCGCGAGCCCTCTGGTAAGGCCCGGCGCGGTGGGGCCCGG A C ME2 Ensembl:ENSG00000082212 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50879086..50879354 26863196 MeRIP-seq:(Medium) rs1307084832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8827505,Human_RBP_ID_9327776 Human_Splice_Rec_1913169,Human_Splice_Rec_1913195,Human_Splice_Rec_1913223,Human_Splice_Rec_1913253,Human_Splice_Rec_1913285,Human_Splice_Rec_1913311,Human_Splice_Rec_1913339,Human_Splice_Rec_1913365,Human_Splice_Rec_1913389,Human_Splice_Rec_1913421,Human_Splice_Rec_1913449,Human_Splice_Rec_1913477,Human_Splice_Rec_1913505 91812 RMVar_ID_91812 Human_SNP_ID_647404107 m1A Human chr18 + 50895754 50895754 50895754 AAATGTGTTTTGAAAACTGATACCCGATGGACATGAAGGCCTATAATATGATTCTCTTCAGTGGT AAATGTGTTTTGAAAACTGATACCCGATGGACGTGAAGGCCTATAATATGATTCTCTTCAGTGGT A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:50895747..50895850 26863196 MeRIP-seq:(Medium) rs919842308 Functional Loss SNV dbSNP153 33..33 33 - - - 91813 RMVar_ID_91813 Human_SNP_ID_647404112 m1A Human chr18 - 50895763 50895763 50895763 AGCAAATAAACCACTGAAGAGAATCATATTATAGGCCTTCATGTCCATCGGGTATCAGTTTTCAA AGCAAATAAACCACTGAAGAGAATCATATTATGGGCCTTCATGTCCATCGGGTATCAGTTTTCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:50895759..50895968 26863196 MeRIP-seq:(Medium) rs1368178481 Functional Loss SNV dbSNP153 33..33 33 - - - 91814 RMVar_ID_91814 Human_SNP_ID_647435569 m1A Human chr18 + 51030284 51030284 51030284 GGCCCTGGTCGTCGTCGCCGCTGCGGTAACGGAGCGGTTTGGGTGGCGGAGCCTGCGTTCGCGCC GGCCCTGGTCGTCGTCGCCGCTGCGGTAACGGGGCGGTTTGGGTGGCGGAGCCTGCGTTCGCGCC A G SMAD4,AC091551.1 Ensembl:ENSG00000141646,Ensembl:ENSG00000267699 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:51030226..51030450 26863196 MeRIP-seq:(Medium) rs1472770123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769346,Human_RBP_ID_4494239,Human_RBP_ID_18420794 91815 RMVar_ID_91815 Human_SNP_ID_647435699 m1A Human chr18 - 51030638 51030638 51030638 GTGCGCGGGCCCGGCCGGGGGAAGGGGAGGGGACATGGCGCGGTTACCTGGGCTCGGGCGGTGGC GTGCGCGGGCCCGGCCGGGGGAAGGGGAGGGGGCATGGCGCGGTTACCTGGGCTCGGGCGGTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:51030636..51030722 26863196 MeRIP-seq:(Medium) rs1053311173 Functional Loss SNV dbSNP153 33..33 33 - - - 91816 RMVar_ID_91816 Human_SNP_ID_647474283 m1A Human chr18 + 51177518 51177518 51177518 CTTCCAGTGACAACAAAAATGGGCTCTTCACCACGAACAGGAGTCTTGATATACGTGTTTGTCTT CTTCCAGTGACAACAAAAATGGGCTCTTCACCGCGAACAGGAGTCTTGATATACGTGTTTGTCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:51177469..51192925 26863196 MeRIP-seq:(Medium) rs1407215504 Functional Loss SNV dbSNP153 33..33 33 - - - 91817 RMVar_ID_91817 Human_SNP_ID_647479044 m1A Human chr18 + 51197112 51197112 51197112 CCTGGCCCTGCGCCGCCGCTGCCGGGGCCCGAAGCGCCGGGGCGCCGGGCTCCGCCGGGCTGGGG CCTGGCCCTGCGCCGCCGCTGCCGGGGCCCGAGGCGCCGGGGCGCCGGGCTCCGCCGGGCTGGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:51197013..51197164 26863410 MeRIP-seq:(Medium) rs1378747197 Functional Loss SNV dbSNP153 33..33 33 - - - 91818 RMVar_ID_91818 Human_SNP_ID_647479117 m1A Human chr18 - 51197262 51197244 51197262 GGCCCTGGCGGCGGCCCCGGCCCCCCTGCCGCAGCCGCCCCCGCCGCCGCCGCCGCCACCGCCGC GGCCCTGGCGGCGGCCCCGGCCCCCCTGCCGC__________________CGCCGCCACCGCCGC GGCGGCGGCGGGGGCGGCT G MEX3C Ensembl:ENSG00000176624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:51196901..51197313 26863196 MeRIP-seq:(Medium) rs1355054814 Functional Loss DEL dbSNP153 33..50 33 - - - 91819 RMVar_ID_91819 Human_SNP_ID_647479131 m1A Human chr18 - 51197262 51197262 51197262 GGCCCTGGCGGCGGCCCCGGCCCCCCTGCCGCAGCCGCCCCCGCCGCCGCCGCCGCCACCGCCGC GGCCCTGGCGGCGGCCCCGGCCCCCCTGCCGCCGCCGCCCCCGCCGCCGCCGCCGCCACCGCCGC T G MEX3C Ensembl:ENSG00000176624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:51196901..51197313 26863196 MeRIP-seq:(Medium) rs1435429007 Functional Loss SNV dbSNP153 33..33 33 - - - 91820 RMVar_ID_91820 Human_SNP_ID_647884188 m1A Human chr18 - 52792808 52792808 52792808 TGGAATAGAATGGAATAGAATGGAATTGAATCAACTGGAATGGAATGGAATGGAATGGAATGGAA TGGAATAGAATGGAATAGAATGGAATTGAATCTACTGGAATGGAATGGAATGGAATGGAATGGAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:52792742..52792874 26863196 MeRIP-seq:(Medium) rs62083268 Functional Loss SNV dbSNP153 33..33 33 - - - 91821 RMVar_ID_91821 Human_SNP_ID_647884189 m1A Human chr18 - 52792808 52792808 52792808 TGGAATAGAATGGAATAGAATGGAATTGAATCAACTGGAATGGAATGGAATGGAATGGAATGGAA TGGAATAGAATGGAATAGAATGGAATTGAATCGACTGGAATGGAATGGAATGGAATGGAATGGAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:52792742..52792874 26863196 MeRIP-seq:(Medium) rs62083268 Functional Loss SNV dbSNP153 33..33 33 - - - 91822 RMVar_ID_91822 Human_SNP_ID_648258803 m1A Human chr18 + 54157811 54157811 54157811 CCCACCCAGCTCAAGTGATGGCTCAAGTGAAAACCCTGAGGCATCCTCGCCACTCTCTCACCCGC CCCACCCAGCTCAAGTGATGGCTCAAGTGAAACCCCTGAGGCATCCTCGCCACTCTCTCACCCGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:54157803..54157935 26863196 MeRIP-seq:(Medium) rs971597333 Functional Loss SNV dbSNP153 33..33 33 - - - 91823 RMVar_ID_91823 Human_SNP_ID_648274479 m1A Human chr18 + 54224096 54224096 54224096 GGATCACTTCCTCCTTCTTCCATCCGGGGGGGAGGGCCGGGCAATCCATCCTCTTCCCGCTCTCC GGATCACTTCCTCCTTCTTCCATCCGGGGGGGGGGGCCGGGCAATCCATCCTCTTCCCGCTCTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr18:54224051..54224625;chr18:54205033..54224192 26863196,32194978 MeRIP-seq:(Medium) rs1221591127 Functional Loss SNV dbSNP153 33..33 33 - - - 91824 RMVar_ID_91824 Human_SNP_ID_648274535 m1A Human chr18 + 54224229 54224199 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGC______________________________GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCCGCCGCCACCGCTGCCGCCGCCGCCGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1281863709 Functional Loss DEL dbSNP153 4..33 33 - - - 91825 RMVar_ID_91825 Human_SNP_ID_648274546 m1A Human chr18 + 54224229 54224211 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACC__________________GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCTGCCGCCGCCGCCGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1425707259 Functional Loss DEL dbSNP153 16..33 33 - - - 91826 RMVar_ID_91826 Human_SNP_ID_648274556 m1A Human chr18 + 54224229 54224214 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCT_______________GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC TGCCGCCGCCGCCGCA T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1555665528 Functional Loss DEL dbSNP153 19..33 33 - - - 91827 RMVar_ID_91827 Human_SNP_ID_648274561 m1A Human chr18 + 54224229 54224217 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCC____________GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCCGCCGCCGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1233231855 Functional Loss DEL dbSNP153 22..33 33 - - - 91828 RMVar_ID_91828 Human_SNP_ID_648274567 m1A Human chr18 + 54224229 54224220 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCC_________GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCCGCCGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1002929606 Functional Loss DEL dbSNP153 25..33 33 - - - 91829 RMVar_ID_91829 Human_SNP_ID_648274572 m1A Human chr18 + 54224229 54224223 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCCGCC______GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCCGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs886547766 Functional Loss DEL dbSNP153 28..33 33 - - - 91830 RMVar_ID_91830 Human_SNP_ID_648274576 m1A Human chr18 + 54224229 54224226 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCCGCCGCC___GCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC CGCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs1411164198 Functional Loss DEL dbSNP153 31..33 33 - - - 91831 RMVar_ID_91831 Human_SNP_ID_648274580 m1A Human chr18 + 54224229 54224229 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCCGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs530077528 Functional Loss SNV dbSNP153 33..33 33 - - - 91832 RMVar_ID_91832 Human_SNP_ID_648274581 m1A Human chr18 + 54224229 54224229 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCGGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs530077528 Functional Loss SNV dbSNP153 33..33 33 - - - 91833 RMVar_ID_91833 Human_SNP_ID_648274596 m1A Human chr18 - 54224265 54224265 54224265 GGGGCCGGGGCCGGGGCCGCGGCCGTCCCCCGAGTGGCGGCAGCGGCCTTGGCGGCGACGGCGGC GGGGCCGGGGCCGGGGCCGCGGCCGTCCCCCGGGTGGCGGCAGCGGCCTTGGCGGCGACGGCGGC T C MBD2 Ensembl:ENSG00000134046 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr18:54224191..54224341 26863410 MeRIP-seq:(Medium) rs1297535405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238750,Human_RBP_ID_905957,Human_RBP_ID_5238105,Human_RBP_ID_5319540,Human_RBP_ID_8194149,Human_RBP_ID_9353513,Human_RBP_ID_9379888,Human_RBP_ID_22064248,Human_RBP_ID_26783149 91834 RMVar_ID_91834 Human_SNP_ID_648274667 m1A Human chr18 - 54224409 54224409 54224409 CGCTCGCCCCGTCCCCGGTGAGCGGCGTGCGCAGGGAAGGCGCTCGGGGCGGCGGCCGTGGCCGG CGCTCGCCCCGTCCCCGGTGAGCGGCGTGCGCGGGGAAGGCGCTCGGGGCGGCGGCCGTGGCCGG T C MBD2 Ensembl:ENSG00000134046 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr18:54224042..54224639;chr18:54224051..54224625 26863196 MeRIP-seq:(Medium) rs1453570602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4489199,Human_RBP_ID_8194585,Human_RBP_ID_8727797,Human_RBP_ID_9327784,Human_RBP_ID_9353514 91835 RMVar_ID_91835 Human_SNP_ID_648286440 m1A Human chr18 + 54269611 54269609 54269611 AGGCGGCGGCGACGACGACGAGGAAGACGCCGAGGCCTGGGCCATGGAACTGGCGGACGTGGGGG AGGCGGCGGCGACGACGACGAGGAAGACGCC__GGCCTGGGCCATGGAACTGGCGGACGTGGGGG CGA C POLI Ensembl:ENSG00000101751 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:54269562..54269812 26863196 MeRIP-seq:(Medium) rs762704706 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18420675,Human_RBP_ID_18993746,Human_RBP_ID_22965727 Human_Splice_Rec_1914351,Human_Splice_Rec_1914369,Human_Splice_Rec_1914385 91836 RMVar_ID_91836 Human_SNP_ID_648308091 m1A Human chr18 - 54357976 54357976 54357976 ACCCGGACACCGCCCCGCCTCAGGCTCGGCTCACTCGCAGCTTCCTCCGCAGTCACAGCAGAGCT ACCCGGACACCGCCCCGCCTCAGGCTCGGCTCCCTCGCAGCTTCCTCCGCAGTCACAGCAGAGCT T G lnc-MBD2-1,lnc-MBD2-1:2 RNACentral:URS00009C355A,RNACentral:URS00008BAF61 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:54357926..54358672 26863196 MeRIP-seq:(Medium) rs542894988 Functional Loss SNV dbSNP153 33..33 33 - - - 91837 RMVar_ID_91837 Human_SNP_ID_648313231 m1A Human chr18 + 54378271 54378271 54378271 AAATGTGAAGAGGAAAATGAAACTGTCACCACAATGAATAGTCACCACAGAACAAATAGGCATTT AAATGTGAAGAGGAAAATGAAACTGTCACCACGATGAATAGTCACCACAGAACAAATAGGCATTT A G C18orf54 Ensembl:ENSG00000166845 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3753056 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_27814611 Human_Splice_Rec_1914550,Human_Splice_Rec_1914560,Human_Splice_Rec_1914572,Human_Splice_Rec_1914586,Human_Splice_Rec_1914600,Human_Splice_Rec_1914608,Human_Splice_Rec_1914610,Human_Splice_Rec_1914611 GWAS_ID_11867,GWAS_ID_11868,GWAS_ID_11869,GWAS_ID_11870,GWAS_ID_11871,GWAS_ID_11872,GWAS_ID_11873,GWAS_ID_11874,GWAS_ID_11875,GWAS_ID_11876,GWAS_ID_11877,GWAS_ID_11878,GWAS_ID_11879,GWAS_ID_11880,GWAS_ID_11881,GWAS_ID_11882,GWAS_ID_11883,GWAS_ID_11884,GWAS_ID_11885,GWAS_ID_11886,GWAS_ID_11887,GWAS_ID_11888,GWAS_ID_11889,GWAS_ID_11890,GWAS_ID_11891,GWAS_ID_11892,GWAS_ID_11893,GWAS_ID_11894,GWAS_ID_11895,GWAS_ID_11896,GWAS_ID_11897,GWAS_ID_11898,GWAS_ID_11899,GWAS_ID_11900,GWAS_ID_11901,GWAS_ID_11902,GWAS_ID_11903,GWAS_ID_11904,GWAS_ID_11905,GWAS_ID_11906,GWAS_ID_11907,GWAS_ID_11908,GWAS_ID_11909,GWAS_ID_11910,GWAS_ID_11911,GWAS_ID_11912,GWAS_ID_11913,GWAS_ID_11914,GWAS_ID_11915,GWAS_ID_11916,GWAS_ID_11917,GWAS_ID_11918,GWAS_ID_11919,GWAS_ID_11920,GWAS_ID_11921,GWAS_ID_11922,GWAS_ID_11923,GWAS_ID_11924,GWAS_ID_11925,GWAS_ID_11926,GWAS_ID_11927,GWAS_ID_11928,GWAS_ID_11929,GWAS_ID_11930,GWAS_ID_11931,GWAS_ID_11932,GWAS_ID_11933,GWAS_ID_11934,GWAS_ID_11935,GWAS_ID_11936,GWAS_ID_11937,GWAS_ID_11938,GWAS_ID_11939,GWAS_ID_11940,GWAS_ID_11941,GWAS_ID_11942,GWAS_ID_11943,GWAS_ID_11944,GWAS_ID_11945,GWAS_ID_11946,GWAS_ID_11947,GWAS_ID_11948,GWAS_ID_11949,GWAS_ID_11950,GWAS_ID_11951,GWAS_ID_11952,GWAS_ID_11953,GWAS_ID_11954,GWAS_ID_11955,GWAS_ID_11956,GWAS_ID_11957,GWAS_ID_11958,GWAS_ID_11959,GWAS_ID_11960,GWAS_ID_11961,GWAS_ID_11962,GWAS_ID_11963,GWAS_ID_11964,GWAS_ID_11965,GWAS_ID_11966,GWAS_ID_11967,GWAS_ID_11968,GWAS_ID_11969,GWAS_ID_11970,GWAS_ID_11971,GWAS_ID_11972,GWAS_ID_11973,GWAS_ID_11974,GWAS_ID_11975,GWAS_ID_11976,GWAS_ID_11977,GWAS_ID_11978,GWAS_ID_11979 91838 RMVar_ID_91838 Human_SNP_ID_648313232 m1A Human chr18 + 54378271 54378271 54378271 AAATGTGAAGAGGAAAATGAAACTGTCACCACAATGAATAGTCACCACAGAACAAATAGGCATTT AAATGTGAAGAGGAAAATGAAACTGTCACCACTATGAATAGTCACCACAGAACAAATAGGCATTT A T C18orf54 Ensembl:ENSG00000166845 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3753056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27814611 Human_Splice_Rec_1914550,Human_Splice_Rec_1914560,Human_Splice_Rec_1914572,Human_Splice_Rec_1914586,Human_Splice_Rec_1914600,Human_Splice_Rec_1914608,Human_Splice_Rec_1914610,Human_Splice_Rec_1914611 GWAS_ID_11867,GWAS_ID_11868,GWAS_ID_11869,GWAS_ID_11870,GWAS_ID_11871,GWAS_ID_11872,GWAS_ID_11873,GWAS_ID_11874,GWAS_ID_11875,GWAS_ID_11876,GWAS_ID_11877,GWAS_ID_11878,GWAS_ID_11879,GWAS_ID_11880,GWAS_ID_11881,GWAS_ID_11882,GWAS_ID_11883,GWAS_ID_11884,GWAS_ID_11885,GWAS_ID_11886,GWAS_ID_11887,GWAS_ID_11888,GWAS_ID_11889,GWAS_ID_11890,GWAS_ID_11891,GWAS_ID_11892,GWAS_ID_11893,GWAS_ID_11894,GWAS_ID_11895,GWAS_ID_11896,GWAS_ID_11897,GWAS_ID_11898,GWAS_ID_11899,GWAS_ID_11900,GWAS_ID_11901,GWAS_ID_11902,GWAS_ID_11903,GWAS_ID_11904,GWAS_ID_11905,GWAS_ID_11906,GWAS_ID_11907,GWAS_ID_11908,GWAS_ID_11909,GWAS_ID_11910,GWAS_ID_11911,GWAS_ID_11912,GWAS_ID_11913,GWAS_ID_11914,GWAS_ID_11915,GWAS_ID_11916,GWAS_ID_11917,GWAS_ID_11918,GWAS_ID_11919,GWAS_ID_11920,GWAS_ID_11921,GWAS_ID_11922,GWAS_ID_11923,GWAS_ID_11924,GWAS_ID_11925,GWAS_ID_11926,GWAS_ID_11927,GWAS_ID_11928,GWAS_ID_11929,GWAS_ID_11930,GWAS_ID_11931,GWAS_ID_11932,GWAS_ID_11933,GWAS_ID_11934,GWAS_ID_11935,GWAS_ID_11936,GWAS_ID_11937,GWAS_ID_11938,GWAS_ID_11939,GWAS_ID_11940,GWAS_ID_11941,GWAS_ID_11942,GWAS_ID_11943,GWAS_ID_11944,GWAS_ID_11945,GWAS_ID_11946,GWAS_ID_11947,GWAS_ID_11948,GWAS_ID_11949,GWAS_ID_11950,GWAS_ID_11951,GWAS_ID_11952,GWAS_ID_11953,GWAS_ID_11954,GWAS_ID_11955,GWAS_ID_11956,GWAS_ID_11957,GWAS_ID_11958,GWAS_ID_11959,GWAS_ID_11960,GWAS_ID_11961,GWAS_ID_11962,GWAS_ID_11963,GWAS_ID_11964,GWAS_ID_11965,GWAS_ID_11966,GWAS_ID_11967,GWAS_ID_11968,GWAS_ID_11969,GWAS_ID_11970,GWAS_ID_11971,GWAS_ID_11972,GWAS_ID_11973,GWAS_ID_11974,GWAS_ID_11975,GWAS_ID_11976,GWAS_ID_11977,GWAS_ID_11978,GWAS_ID_11979 91839 RMVar_ID_91839 Human_SNP_ID_648851570 m1A Human chr18 + 56638447 56638447 56638447 CTCCCGACGGGCTTCACCCCCACCATCCTCACAGAGAGCCCGGCAGGGTGGCCGCGACGCCACTG CTCCCGACGGGCTTCACCCCCACCATCCTCACTGAGAGCCCGGCAGGGTGGCCGCGACGCCACTG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:56638401..56638600 26863196 MeRIP-seq:(Medium) rs1234429190 Functional Loss SNV dbSNP153 33..33 33 - - - 91840 RMVar_ID_91840 Human_SNP_ID_648851573 m1A Human chr18 + 56638451 56638451 56638451 CGACGGGCTTCACCCCCACCATCCTCACAGAGAGCCCGGCAGGGTGGCCGCGACGCCACTGGCTT CGACGGGCTTCACCCCCACCATCCTCACAGAGCGCCCGGCAGGGTGGCCGCGACGCCACTGGCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:56638405..56638625 26863196 MeRIP-seq:(Medium) rs138658242 Functional Loss SNV dbSNP153 33..33 33 - - - 91841 RMVar_ID_91841 Human_SNP_ID_648851574 m1A Human chr18 + 56638451 56638451 56638451 CGACGGGCTTCACCCCCACCATCCTCACAGAGAGCCCGGCAGGGTGGCCGCGACGCCACTGGCTT CGACGGGCTTCACCCCCACCATCCTCACAGAGGGCCCGGCAGGGTGGCCGCGACGCCACTGGCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:56638405..56638625 26863196 MeRIP-seq:(Medium) rs138658242 Functional Loss SNV dbSNP153 33..33 33 - - - 91842 RMVar_ID_91842 Human_SNP_ID_648851612 m1A Human chr18 - 56638528 56638525 56638529 CCACCTCTTCTGTCCAGGCCTCGGCCTTCCTGAGCATCTCTCCTTCCTCTCCCAGATCGTCTTCT CCACCTCTTCTGTCCAGGCCTCGGCCTTCCT____ATCTCTCCTTCCTCTCCCAGATCGTCTTCT TGCTC T TXNL1 Ensembl:ENSG00000091164 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:56638351..56638650 26863196 MeRIP-seq:(Medium) rs532171740 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_509584,Human_RBP_ID_1550814,Human_RBP_ID_4489626,Human_RBP_ID_5468141,Human_RBP_ID_5498588,Human_RBP_ID_18718356,Human_RBP_ID_18944321 91843 RMVar_ID_91843 Human_SNP_ID_648876456 m1A Human chr18 - 56743850 56743850 56743850 AAATCGCCCACTCTCTCATCCCCTGGAAACCTAGCTTCATCAATTATCAATTCCTCCCTATCCTG AAATCGCCCACTCTCTCATCCCCTGGAAACCTCGCTTCATCAATTATCAATTCCTCCCTATCCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:56743803..56743921 26863196 MeRIP-seq:(Medium) rs773437552 Functional Loss SNV dbSNP153 33..33 33 - - - 91844 RMVar_ID_91844 Human_SNP_ID_648921594 m1A Human chr18 - 56938569 56938569 56938569 TGCAAGAGTTGTTGTGTGCATATTCTGCTGTGATTGGGTATTTGCTGCAAGAGCCGTATGTCTGT TGCAAGAGTTGTTGTGTGCATATTCTGCTGTGTTTGGGTATTTGCTGCAAGAGCCGTATGTCTGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:56938504..56938569 26863196 MeRIP-seq:(Medium) rs768367141 Functional Loss SNV dbSNP153 33..33 33 - - - 91845 RMVar_ID_91845 Human_SNP_ID_649040614 m1A Human chr18 + 57435538 57435537 57435538 CCCTCTCCCGCACGCACGCCCCGTCCGCCCCCACCCCGCCCCCACCCCGGGCGAGCCCGCCCGCA CCCTCTCCCGCACGCACGCCCCGTCCGCCCCC_CCCCGCCCCCACCCCGGGCGAGCCCGCCCGCA CA C ONECUT2 Ensembl:ENSG00000119547 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:57435446..57435609 26863410 MeRIP-seq:(Medium) rs1344660668 Functional Loss DEL dbSNP153 33..33 33 - - - 91846 RMVar_ID_91846 Human_SNP_ID_649040616 m1A Human chr18 + 57435538 57435538 57435538 CCCTCTCCCGCACGCACGCCCCGTCCGCCCCCACCCCGCCCCCACCCCGGGCGAGCCCGCCCGCA CCCTCTCCCGCACGCACGCCCCGTCCGCCCCCCCCCCGCCCCCACCCCGGGCGAGCCCGCCCGCA A C ONECUT2 Ensembl:ENSG00000119547 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:57435446..57435609 26863410 MeRIP-seq:(Medium) rs967916223 Functional Loss SNV dbSNP153 33..33 33 - - - 91847 RMVar_ID_91847 Human_SNP_ID_649040760 m1A Human chr18 - 57435836 57435824 57435836 CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCCACTGCCGCCGCCGGCCGGCCCGTGCAAAGTGCC CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCC____________GGCCGGCCCGTGCAAAGTGCC CGGCGGCGGCAGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:57435428..57435947 26863196 MeRIP-seq:(Medium) rs776563143 Functional Loss DEL dbSNP153 33..44 33 - - - 91848 RMVar_ID_91848 Human_SNP_ID_649040763 m1A Human chr18 - 57435836 57435827 57435836 CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCCACTGCCGCCGCCGGCCGGCCCGTGCAAAGTGCC CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCC_________GCCGGCCGGCCCGTGCAAAGTGCC CGGCGGCAGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:57435428..57435947 26863196 MeRIP-seq:(Medium) rs759677858 Functional Loss DEL dbSNP153 33..41 33 - - - 91849 RMVar_ID_91849 Human_SNP_ID_649040770 m1A Human chr18 - 57435836 57435836 57435836 CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCCACTGCCGCCGCCGGCCGGCCCGTGCAAAGTGCC CCGCCCCCGCCGCCCCCGCCGCCGCCCCCGCCGCTGCCGCCGCCGGCCGGCCCGTGCAAAGTGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:57435428..57435947 26863196 MeRIP-seq:(Medium) rs1568116422 Functional Loss SNV dbSNP153 33..33 33 - - - 91850 RMVar_ID_91850 Human_SNP_ID_649040815 m1A Human chr18 + 57435886 57435886 57435886 GGGCGGCGGGGGCGGCGGCGGGGGCCCGGGCCATGAGCAGGAGCTGCTGGCCAGCCCCAGCCCCC GGGCGGCGGGGGCGGCGGCGGGGGCCCGGGCCCTGAGCAGGAGCTGCTGGCCAGCCCCAGCCCCC A C ONECUT2 Ensembl:ENSG00000119547 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:57435431..57435888;chr18:57435740..57435904;chr18:57435830..57435913 26863196 MeRIP-seq:(Medium) rs1315311088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_379446,Human_miRNA_ID_486214,Human_miRNA_ID_599390,Human_miRNA_ID_1045979,Human_miRNA_ID_1347792,Human_miRNA_ID_1455901 91851 RMVar_ID_91851 Human_SNP_ID_649040816 m1A Human chr18 + 57435886 57435886 57435886 GGGCGGCGGGGGCGGCGGCGGGGGCCCGGGCCATGAGCAGGAGCTGCTGGCCAGCCCCAGCCCCC GGGCGGCGGGGGCGGCGGCGGGGGCCCGGGCCGTGAGCAGGAGCTGCTGGCCAGCCCCAGCCCCC A G ONECUT2 Ensembl:ENSG00000119547 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:57435431..57435888;chr18:57435740..57435904;chr18:57435830..57435913 26863196 MeRIP-seq:(Medium) rs1315311088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_379446,Human_miRNA_ID_486214,Human_miRNA_ID_599390,Human_miRNA_ID_1045979,Human_miRNA_ID_1347792,Human_miRNA_ID_1455901 91852 RMVar_ID_91852 Human_SNP_ID_649040942 m1A Human chr18 + 57436159 57436159 57436159 GTCTCCGCCTGGCATGGGCATGAGCAACACCTACACCACGCTGACACCGCTCCAGCCGCTGCCAC GTCTCCGCCTGGCATGGGCATGAGCAACACCTTCACCACGCTGACACCGCTCCAGCCGCTGCCAC A T ONECUT2 Ensembl:ENSG00000119547 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:57436108..57436415 26863196 MeRIP-seq:(Medium) rs1420294135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17381257 91853 RMVar_ID_91853 Human_SNP_ID_649079606 m1A Human chr18 - 57600855 57600855 57600855 ATAAATAAGTTCCAAAAGAAATTGTAGCTGGAATCTTAATAACAATTGTGAGTGGCTGTTTGAGT ATAAATAAGTTCCAAAAGAAATTGTAGCTGGAGTCTTAATAACAATTGTGAGTGGCTGTTTGAGT T C NARS1 Ensembl:ENSG00000134440 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:57600805..57600905 32194978 MeRIP-seq:(Medium) rs1002058879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_509830,Human_RBP_ID_1012241,Human_RBP_ID_1877037,Human_RBP_ID_2545120,Human_RBP_ID_3557949,Human_RBP_ID_5115827,Human_RBP_ID_6696881,Human_RBP_ID_8194587,Human_RBP_ID_17496986,Human_RBP_ID_17911209,Human_RBP_ID_18300080,Human_RBP_ID_23210666,Human_RBP_ID_23774472,Human_RBP_ID_26462679,Human_RBP_ID_26649726,Human_RBP_ID_27673202 RMVar_hsa_circ_190322,RMVar_hsa_circ_118035,RMVar_hsa_circ_120281,RMVar_hsa_circ_121799,RMVar_hsa_circ_120937,RMVar_hsa_circ_119396,RMVar_hsa_circ_110138,RMVar_hsa_circ_114273,RMVar_hsa_circ_190324,RMVar_hsa_circ_190325,RMVar_hsa_circ_190326,RMVar_hsa_circ_190323,RMVar_hsa_circ_190320,RMVar_hsa_circ_190321 91854 RMVar_ID_91854 Human_SNP_ID_649081272 m1A Human chr18 - 57606660 57606660 57606660 TGGAGGACTTGGTTTGTGATGTGGTAGATCGAATATTGAAGTCACCTGCAGGGAGCATAGTGCAT TGGAGGACTTGGTTTGTGATGTGGTAGATCGAGTATTGAAGTCACCTGCAGGGAGCATAGTGCAT T C NARS1 Ensembl:ENSG00000134440 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:57602871..57606779 32194978 MeRIP-seq:(Medium) rs1239312817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1550942,Human_RBP_ID_1877064,Human_RBP_ID_6696961,Human_RBP_ID_8473074,Human_RBP_ID_8827777,Human_RBP_ID_17694080,Human_RBP_ID_17913469 Human_Splice_Rec_1917790,Human_Splice_Rec_1917791,Human_Splice_Rec_1917816,Human_Splice_Rec_1917817,Human_Splice_Rec_1917825 Human_miRNA_ID_2376950,Human_miRNA_ID_3032597 RMVar_hsa_circ_190322,RMVar_hsa_circ_120281,RMVar_hsa_circ_119396,RMVar_hsa_circ_110138,RMVar_hsa_circ_114273,RMVar_hsa_circ_190323,RMVar_hsa_circ_28981,RMVar_hsa_circ_190320,RMVar_hsa_circ_190321,RMVar_hsa_circ_60020,RMVar_hsa_circ_333218,RMVar_hsa_circ_190328,RMVar_hsa_circ_98740,RMVar_hsa_circ_19453,RMVar_hsa_circ_100129,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190327 91855 RMVar_ID_91855 Human_SNP_ID_649081574 m1A Human chr18 + 57607562 57607562 57607562 CTCGGATCATCATGTGTCTGTTGTTGAGCTGGACATCAACGTCAGACTCCTCATTGATCAGGTTG CTCGGATCATCATGTGTCTGTTGTTGAGCTGGTCATCAACGTCAGACTCCTCATTGATCAGGTTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:57607476..57607675 32194978 MeRIP-seq:(Medium) rs749969311 Functional Loss SNV dbSNP153 33..33 33 - - - 91856 RMVar_ID_91856 Human_SNP_ID_649083156 m1A Human chr18 - 57613653 57613653 57613653 GACAGGTGAAGATTGGTGCGTTAGAAGGATATAGAGGCCAAAGAGTAAAGGTGTTTGGCTGGGTC GACAGGTGAAGATTGGTGCGTTAGAAGGATATGGAGGCCAAAGAGTAAAGGTGTTTGGCTGGGTC T C NARS1 Ensembl:ENSG00000134440 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:57613601..57613729 26863196 MeRIP-seq:(Medium) rs1310083519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7192,Human_RBP_ID_51696,Human_RBP_ID_201973,Human_RBP_ID_906530,Human_RBP_ID_1067094,Human_RBP_ID_1552764,Human_RBP_ID_2545136,Human_RBP_ID_3953615,Human_RBP_ID_4496289,Human_RBP_ID_6697000,Human_RBP_ID_8232816,Human_RBP_ID_8827803,Human_RBP_ID_9379656,Human_RBP_ID_17913472,Human_RBP_ID_18412155,Human_RBP_ID_18718555,Human_RBP_ID_18993441,Human_RBP_ID_19028699,Human_RBP_ID_23114593,Human_RBP_ID_23774525,Human_RBP_ID_24545342,Human_RBP_ID_26334453,Human_RBP_ID_27814622 Human_Splice_Rec_1917780,Human_Splice_Rec_1917781,Human_Splice_Rec_1917810,Human_Splice_Rec_1917832,Human_Splice_Rec_1917833,Human_Splice_Rec_1917846,Human_Splice_Rec_1917847,Human_Splice_Rec_1917858,Human_Splice_Rec_1917859,Human_Splice_Rec_1917870,Human_Splice_Rec_1917871,Human_Splice_Rec_1917882,Human_Splice_Rec_1917883,Human_Splice_Rec_1917896,Human_Splice_Rec_1917897,Human_Splice_Rec_1917906,Human_Splice_Rec_1917912 RMVar_hsa_circ_119396,RMVar_hsa_circ_110138,RMVar_hsa_circ_32091,RMVar_hsa_circ_28981,RMVar_hsa_circ_190320,RMVar_hsa_circ_190321,RMVar_hsa_circ_333218,RMVar_hsa_circ_190328,RMVar_hsa_circ_98740,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_346699,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_277711,RMVar_hsa_circ_66251,RMVar_hsa_circ_190332,RMVar_hsa_circ_190333,RMVar_hsa_circ_190334,RMVar_hsa_circ_326300 91857 RMVar_ID_91857 Human_SNP_ID_649085571 m1A Human chr18 - 57621755 57621755 57621755 ACGTTGGAGTCATAAGACGGCGTCGGTGTTGCAGTCTGTGTCCTTGGAGGTGACCAGGGCCACTG ACGTTGGAGTCATAAGACGGCGTCGGTGTTGCGGTCTGTGTCCTTGGAGGTGACCAGGGCCACTG T C NARS1 Ensembl:ENSG00000134440 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:57615595..57621825 26863196 MeRIP-seq:(Medium) rs367591907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51700,Human_RBP_ID_238585,Human_RBP_ID_509876,Human_RBP_ID_1550984,Human_RBP_ID_4494247,Human_RBP_ID_5420965,Human_RBP_ID_6697057,Human_RBP_ID_8827807,Human_RBP_ID_9291015,Human_RBP_ID_13325406,Human_RBP_ID_18718566,Human_RBP_ID_23774538,Human_RBP_ID_26334752 Human_Splice_Rec_1917773,Human_Splice_Rec_1917803,Human_Splice_Rec_1917827,Human_Splice_Rec_1917839,Human_Splice_Rec_1917853,Human_Splice_Rec_1917865,Human_Splice_Rec_1917877,Human_Splice_Rec_1917889,Human_Splice_Rec_1917899,Human_Splice_Rec_1917907 Human_miRNA_ID_1959649,Human_miRNA_ID_2017041 RMVar_hsa_circ_88227,RMVar_hsa_circ_190332 91858 RMVar_ID_91858 Human_SNP_ID_649122450 m1A Human chr18 - 57764248 57764245 57764249 AGGAAGGAAGGAAGGAAAGAAGGAAGGAAGGAAGGCAGGCTCCCTGGGGCAGGTGGCTGCACAGT AGGAAGGAAGGAAGGAAAGAAGGAAGGAAGG____CAGGCTCCCTGGGGCAGGTGGCTGCACAGT GCCTT G ATP8B1 Ensembl:ENSG00000081923 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:57764231..57764409 26863196 MeRIP-seq:(Medium) rs564194950 Functional Loss DEL dbSNP153 32..35 33 - - - 91859 RMVar_ID_91859 Human_SNP_ID_649122497 m1A Human chr18 - 57764319 57764319 57764319 AAGAAAGAAAAAGAAAGAAAGAAAGAAAAAGAAAGAAAGAAAGAAGGAAGGAAGAAAAGAAGAAA AAGAAAGAAAAAGAAAGAAAGAAAGAAAAAGAGAGAAAGAAAGAAGGAAGGAAGAAAAGAAGAAA T C ATP8B1 Ensembl:ENSG00000081923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:57764316..57764413 26863196 MeRIP-seq:(Medium) rs1413215182 Functional Loss SNV dbSNP153 33..33 33 - - - 91860 RMVar_ID_91860 Human_SNP_ID_649131770 m1A Human chr18 - 57803295 57803295 57803295 TGGAGGGAAACCAGAGGCACCTCCCCGAGCGGAGAAACCAGTTTGGCCGGTCCGGCGGAGCGGAG TGGAGGGAAACCAGAGGCACCTCCCCGAGCGGCGAAACCAGTTTGGCCGGTCCGGCGGAGCGGAG T G ATP8B1 Ensembl:ENSG00000081923 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:57802994..57803343;chr18:57803015..57803334 26863196 MeRIP-seq:(Medium) rs779313611 Functional Loss SNV dbSNP153 33..33 33 - - - 91861 RMVar_ID_91861 Human_SNP_ID_649191155 m1A Human chr18 + 58044592 58044592 58044592 TGCGGGACCGGGGGGACCTGGAGGCAGAGGGGAGAACCGGCCGTCCGCGCCGCAGCACAGCCGCT TGCGGGACCGGGGGGACCTGGAGGCAGAGGGGCGAACCGGCCGTCCGCGCCGCAGCACAGCCGCT A C NEDD4L Ensembl:ENSG00000049759 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:58044137..58044701 26863196 MeRIP-seq:(Medium) rs568694817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769361,Human_RBP_ID_823082,Human_RBP_ID_4494030,Human_RBP_ID_5144558,Human_RBP_ID_9424742 RMVar_hsa_circ_268658 91862 RMVar_ID_91862 Human_SNP_ID_649191384 m1A Human chr18 + 58045078 58045078 58045078 CAACTTTCCGCCTCTCGCCCCTGCAGCCCGGGAGTCCATGATGCATGTCACGTCTGGGTCGCGCG CAACTTTCCGCCTCTCGCCCCTGCAGCCCGGGGGTCCATGATGCATGTCACGTCTGGGTCGCGCG A G NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58045067..58045183 26863196 MeRIP-seq:(Medium) rs1291965859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7194,Human_RBP_ID_5189566,Human_RBP_ID_18460700,Human_RBP_ID_19087730,Human_RBP_ID_22545096,Human_RBP_ID_22965728,Human_RBP_ID_23119078,Human_RBP_ID_25377183 Human_Splice_Rec_1918302 91863 RMVar_ID_91863 Human_SNP_ID_649222215 m1A Human chr18 - 58165735 58165731 58165735 AAAGAGGTTAAAAACCTGATCTTCAATCAATCACTCTCTCATCCAATATTAAAGTAATTGATTTC AAAGAGGTTAAAAACCTGATCTTCAATCAATC____TCTCATCCAATATTAAAGTAATTGATTTC AGAGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58165733..58165821 26863196 MeRIP-seq:(Medium) rs1450888501 Functional Loss DEL dbSNP153 33..36 33 - - - 91864 RMVar_ID_91864 Human_SNP_ID_649265145 m1A Human chr18 + 58341770 58341770 58341770 CAGATCCGCCGGCCTCGTAGCCTCAGCTCGCCAACAGTAACTTTATCTGCCCCGCTGGAGGTGAG CAGATCCGCCGGCCTCGTAGCCTCAGCTCGCCGACAGTAACTTTATCTGCCCCGCTGGAGGTGAG A G NEDD4L Ensembl:ENSG00000049759 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:58341719..58341845 26863196 MeRIP-seq:(Medium) rs1243516401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9379664,Human_RBP_ID_19087272,Human_RBP_ID_26334464 Human_Splice_Rec_1918206,Human_Splice_Rec_1918207,Human_Splice_Rec_1918262,Human_Splice_Rec_1918263,Human_Splice_Rec_1918328,Human_Splice_Rec_1918329,Human_Splice_Rec_1918472,Human_Splice_Rec_1918473,Human_Splice_Rec_1918536,Human_Splice_Rec_1918537,Human_Splice_Rec_1918596,Human_Splice_Rec_1918597,Human_Splice_Rec_1918654,Human_Splice_Rec_1918655,Human_Splice_Rec_1918710,Human_Splice_Rec_1918711,Human_Splice_Rec_1918796,Human_Splice_Rec_1918797,Human_Splice_Rec_1918894,Human_Splice_Rec_1918895,Human_Splice_Rec_1918988,Human_Splice_Rec_1918989 Human_miRNA_ID_295897,Human_miRNA_ID_1752221,Human_miRNA_ID_2063908,Human_miRNA_ID_2063909,Human_miRNA_ID_2901570,Human_miRNA_ID_2901571,Human_miRNA_ID_2914866,Human_miRNA_ID_2914867,Human_miRNA_ID_3066311,Human_miRNA_ID_3066312 RMVar_hsa_circ_6445,RMVar_hsa_circ_335897,RMVar_hsa_circ_59427,RMVar_hsa_circ_86834,RMVar_hsa_circ_190368,RMVar_hsa_circ_308097,RMVar_hsa_circ_41951,RMVar_hsa_circ_336369,RMVar_hsa_circ_74837,RMVar_hsa_circ_342028,RMVar_hsa_circ_366054,RMVar_hsa_circ_326822,RMVar_hsa_circ_335721,RMVar_hsa_circ_320171,RMVar_hsa_circ_190378,RMVar_hsa_circ_190380,RMVar_hsa_circ_288977,RMVar_hsa_circ_190379,RMVar_hsa_circ_190377 91865 RMVar_ID_91865 Human_SNP_ID_649265496 m1A Human chr18 - 58342981 58342981 58342981 TGTGACTTTGTGTTGTGGTTTGGGGGAGTTGTAAGGTGATGGCTGTGGGGACTGTGGGTTGGAAA TGTGACTTTGTGTTGTGGTTTGGGGGAGTTGTGAGGTGATGGCTGTGGGGACTGTGGGTTGGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58342931..58343018 26863196 MeRIP-seq:(Medium) rs1172516695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190382 91866 RMVar_ID_91866 Human_SNP_ID_649300926 m1A Human chr18 + 58483415 58483415 58483415 TGCACTGTCTGGCTGCATCTCCCAACCCATTGACCTCTTCAGCCATTAGAAGTGTGTCCAAGCTC TGCACTGTCTGGCTGCATCTCCCAACCCATTGTCCTCTTCAGCCATTAGAAGTGTGTCCAAGCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58483365..58483466 26863196 MeRIP-seq:(Medium) rs1234220619 Functional Loss SNV dbSNP153 33..33 33 - - - 91867 RMVar_ID_91867 Human_SNP_ID_649303326 m1A Human chr18 - 58492496 58492496 58492496 GTGACAGAGCCTGAGTGGACAGCATGGGGTGAAGACCAGAATAGACAAGAAAAAGGTTATCACTG GTGACAGAGCCTGAGTGGACAGCATGGGGTGACGACCAGAATAGACAAGAAAAAGGTTATCACTG T G ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58492445..58492548 26863196 MeRIP-seq:(Medium) rs1294032718 Functional Loss SNV dbSNP153 33..33 33 - - - 91868 RMVar_ID_91868 Human_SNP_ID_649313574 m1A Human chr18 - 58535080 58535080 58535080 AAGCCCGAGCAGGCAAATCGCCAGGGACCCTCACAGCAGTGACGGGGTCAGAGGAGGTCAAGAGG AAGCCCGAGCAGGCAAATCGCCAGGGACCCTCGCAGCAGTGACGGGGTCAGAGGAGGTCAAGAGG T C ALPK2 Ensembl:ENSG00000198796 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:58535030..58535150 26863196 MeRIP-seq:(Medium) rs1568077131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_189961 RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390,RMVar_hsa_circ_363395 91869 RMVar_ID_91869 Human_SNP_ID_649317463 m1A Human chr18 - 58550327 58550326 58550327 CAGAGATGGGGTTGTTCATGATGAAGGCAGGGATAGGGTTTTACGTGATGGAGATGGGGATGGGG CAGAGATGGGGTTGTTCATGATGAAGGCAGGG_TAGGGTTTTACGTGATGGAGATGGGGATGGGG AT A ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58550289..58550383 26863196 MeRIP-seq:(Medium) rs1317856376 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390 91870 RMVar_ID_91870 Human_SNP_ID_649317486 m1A Human chr18 + 58550370 58550370 58550370 ATCATGAACAACCCCATCTCTGTCTCTATCACATACAACCCCATCCCCATCTCCATCACCTACAA ATCATGAACAACCCCATCTCTGTCTCTATCACCTACAACCCCATCCCCATCTCCATCACCTACAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:58550197..58550406 26863196 MeRIP-seq:(Medium) rs111768148 Functional Loss SNV dbSNP153 33..33 33 - - - 91871 RMVar_ID_91871 Human_SNP_ID_649317748 m1A Human chr18 - 58550796 58550796 58550796 ATATGATGGAGATAGGGATGAGGTTGTATGTGATGGAGATGTGGATGGGGTTGTACATGATAGAG ATATGATGGAGATAGGGATGAGGTTGTATGTGTTGGAGATGTGGATGGGGTTGTACATGATAGAG T A ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58550757..58550997 26863196 MeRIP-seq:(Medium) rs1470817993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390 91872 RMVar_ID_91872 Human_SNP_ID_649324854 m1A Human chr18 - 58579044 58579044 58579044 CCAAAGAATCTGCTGAGCCCCCACTAACCCAGAGTGATAAAAGAGAGACTTCTCACACCACAGCA CCAAAGAATCTGCTGAGCCCCCACTAACCCAGCGTGATAAAAGAGAGACTTCTCACACCACAGCA T G ALPK2 Ensembl:ENSG00000198796 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:58578994..58579286 26863196 MeRIP-seq:(Medium) rs750633796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2425508,Human_miRNA_ID_2435176,Human_miRNA_ID_2784687 RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390,RMVar_hsa_circ_42273,RMVar_hsa_circ_312848 91873 RMVar_ID_91873 Human_SNP_ID_649346448 m1A Human chr18 - 58671534 58671532 58671535 TCGCCTCCGAGCCGCGGAGGCAGGGGCGGAAGAACAAATCTGGCAGCGCGGCACGGCCCTCAGAG TCGCCTCCGAGCCGCGGAGGCAGGGGCGGAA___CAAATCTGGCAGCGCGGCACGGCCCTCAGAG GTTC G AC104971.1 Ensembl:ENSG00000267226 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:58671476..58671675 26863196 MeRIP-seq:(Medium) rs1287985110 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1919111 91874 RMVar_ID_91874 Human_SNP_ID_649393991 m1A Human chr18 + 58864609 58864609 58864609 TGTGGGGTGGAGGGGAGGGGGGATGGGCCCTGAGGGGCTCTGGGGTGCTTGCGAGGTGAGCATTT TGTGGGGTGGAGGGGAGGGGGGATGGGCCCTGGGGGGCTCTGGGGTGCTTGCGAGGTGAGCATTT A G ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:58864607..58864776 26863196 MeRIP-seq:(Medium) rs1397909708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86662,RMVar_hsa_circ_190408 91875 RMVar_ID_91875 Human_SNP_ID_649395662 m1A Human chr18 - 58870977 58870977 58870977 TCTCTGTTTTATGTTCATTACTACCAATCTTGACCTCCAGCCCAAGCAACCCTCCTAAATTCCAG TCTCTGTTTTATGTTCATTACTACCAATCTTGTCCTCCAGCCCAAGCAACCCTCCTAAATTCCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:58870939..58871097 26863196 MeRIP-seq:(Medium) rs1568205719 Functional Loss SNV dbSNP153 33..33 33 - - - 91876 RMVar_ID_91876 Human_SNP_ID_649464301 m1A Human chr18 + 59146447 59146447 59146447 TAGTTAGCCTGATGGGACCAATGCCAGCATTCAGGTAGAGGAGGAGATTCAGGTAGAGGAGGAGC TAGTTAGCCTGATGGGACCAATGCCAGCATTCTGGTAGAGGAGGAGATTCAGGTAGAGGAGGAGC A T SEC11C Ensembl:ENSG00000166562 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:59146440..59146802 26863196 MeRIP-seq:(Medium) rs896794962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6697988 91877 RMVar_ID_91877 Human_SNP_ID_649513537 m1A Human chr18 - 59338558 59338558 59338558 AGCATGAGATTCTGAGACAAGTAAATGAAATGAAGTAAGTATGGAAAAGTAGCGTTTGTGTGTTA AGCATGAGATTCTGAGACAAGTAAATGAAATGGAGTAAGTATGGAAAAGTAGCGTTTGTGTGTTA T C LMAN1 Ensembl:ENSG00000074695 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:59338551..59338650 32194978 MeRIP-seq:(Medium) rs1234011224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22964738 Human_Splice_Rec_1919708,Human_Splice_Rec_1919709 RMVar_hsa_circ_46,RMVar_hsa_circ_117284,RMVar_hsa_circ_70372,RMVar_hsa_circ_190439,RMVar_hsa_circ_190441,RMVar_hsa_circ_107644,RMVar_hsa_circ_42688,RMVar_hsa_circ_301525 91878 RMVar_ID_91878 Human_SNP_ID_649517342 m1A Human chr18 - 59353299 59353299 59353299 TTGTCTGTTTTCCTCCCCCTTACACTATAGTGACGGGGCTAGTCAAGCTTTGGCAAGTTGCCAGA TTGTCTGTTTTCCTCCCCCTTACACTATAGTGGCGGGGCTAGTCAAGCTTTGGCAAGTTGCCAGA T C LMAN1 Ensembl:ENSG00000074695 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:59353276..59353325 32194978 MeRIP-seq:(Medium) rs1390127438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768880,Human_RBP_ID_906655,Human_RBP_ID_4490380,Human_RBP_ID_17381654,Human_RBP_ID_22661072,Human_RBP_ID_22762446 Human_Splice_Rec_1919698,Human_Splice_Rec_1919699,Human_Splice_Rec_1919732 RMVar_hsa_circ_46,RMVar_hsa_circ_117284,RMVar_hsa_circ_70372,RMVar_hsa_circ_190439,RMVar_hsa_circ_190441,RMVar_hsa_circ_107644,RMVar_hsa_circ_301525,RMVar_hsa_circ_50504,RMVar_hsa_circ_350499,RMVar_hsa_circ_88321,RMVar_hsa_circ_332233,RMVar_hsa_circ_190442,RMVar_hsa_circ_359904,RMVar_hsa_circ_302565 91879 RMVar_ID_91879 Human_SNP_ID_649517901 m1A Human chr18 - 59355418 59355418 59355418 CTCTAACTGTTCCCTATTACATATTTTCAGGCAATTTGGTATGCAGAAAATCAAGGCTTGGAGGG CTCTAACTGTTCCCTATTACATATTTTCAGGCGATTTGGTATGCAGAAAATCAAGGCTTGGAGGG T C LMAN1 Ensembl:ENSG00000074695 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:59355416..59355483 26863196 MeRIP-seq:(Medium) rs1344472838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17670124,Human_RBP_ID_22446112,Human_RBP_ID_22762393,Human_RBP_ID_25369535,Human_RBP_ID_26334242 Human_Splice_Rec_1919694,Human_Splice_Rec_1919728 RMVar_hsa_circ_117284,RMVar_hsa_circ_190439,RMVar_hsa_circ_301525,RMVar_hsa_circ_50836,RMVar_hsa_circ_50504,RMVar_hsa_circ_350499,RMVar_hsa_circ_88321,RMVar_hsa_circ_332233,RMVar_hsa_circ_190442,RMVar_hsa_circ_359904,RMVar_hsa_circ_302565 91880 RMVar_ID_91880 Human_SNP_ID_649518960 m1A Human chr18 + 59359129 59359129 59359129 ATTTGTACTCGAAACGGCGATGTGGCAACGCGACCGCGGGGTCTCCTCCCACGCCGTCGCCCCGG ATTTGTACTCGAAACGGCGATGTGGCAACGCGGCCGCGGGGTCTCCTCCCACGCCGTCGCCCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:59359083..59359250 26863196 MeRIP-seq:(Medium) rs33926449 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_523,Clinvar_Rec_524 GWAS_ID_11980,GWAS_ID_11981,GWAS_ID_11982,GWAS_ID_11983,GWAS_ID_11984,GWAS_ID_11985,GWAS_ID_11986,GWAS_ID_11987,GWAS_ID_11988,GWAS_ID_11989,GWAS_ID_11990,GWAS_ID_11991,GWAS_ID_11992,GWAS_ID_11993,GWAS_ID_11994,GWAS_ID_11995,GWAS_ID_11996 91881 RMVar_ID_91881 Human_SNP_ID_649611628 m1A Human chr18 - 59697235 59697235 59697235 CTCCTGGCGTTGGGACACACGTGGACCTACAGAGAGGAGCCGGAGGACGGCGACAGGTAAGCGCT CTCCTGGCGTTGGGACACACGTGGACCTACAGGGAGGAGCCGGAGGACGGCGACAGGTAAGCGCT T C CCBE1 Ensembl:ENSG00000183287 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:59696605..59697473 32194978 MeRIP-seq:(Medium) rs1254568069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1919735,Human_Splice_Rec_1919757,Human_Splice_Rec_1919803 91882 RMVar_ID_91882 Human_SNP_ID_649661697 m1A Human chr18 + 59900112 59900108 59900112 TTCGTGTTCAGCTCGCGTCCTGCAGCTGTCCGAGGTGCTCCAGTTGGAGGCTGAGGTTCCCGGGC TTCGTGTTCAGCTCGCGTCCTGCAGCTGT____GGTGCTCCAGTTGGAGGCTGAGGTTCCCGGGC TCCGA T PMAIP1 Ensembl:ENSG00000141682 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:59900063..59900189 26863196 MeRIP-seq:(Medium) rs1301270233 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_510125,Human_RBP_ID_769108,Human_RBP_ID_1186524,Human_RBP_ID_1551132,Human_RBP_ID_1877316,Human_RBP_ID_3558253,Human_RBP_ID_4490408,Human_RBP_ID_5442480,Human_RBP_ID_6698382,Human_RBP_ID_8473353,Human_RBP_ID_13327477,Human_RBP_ID_18718773,Human_RBP_ID_22227529,Human_RBP_ID_23775232,Human_RBP_ID_26814468 RMVar_hsa_circ_118304,RMVar_hsa_circ_190454 91883 RMVar_ID_91883 Human_SNP_ID_649661722 m1A Human chr18 + 59900168 59900168 59900168 TTCCCGGGCTCTGTAGCTGAGTGGGCGGCGGCACCGGCGGAGATGCCTGGGAAGAAGGCGCGCAA TTCCCGGGCTCTGTAGCTGAGTGGGCGGCGGCGCCGGCGGAGATGCCTGGGAAGAAGGCGCGCAA A G PMAIP1 Ensembl:ENSG00000141682 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:59900056..59900173;chr18:59900001..59900264 26863196 MeRIP-seq:(Medium) rs1177642095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238639,Human_RBP_ID_279066,Human_RBP_ID_1012305,Human_RBP_ID_1551136,Human_RBP_ID_4490409,Human_RBP_ID_6698385,Human_RBP_ID_13327479,Human_RBP_ID_22445916,Human_RBP_ID_25379264,Human_RBP_ID_27265769 Human_Splice_Rec_1919845,Human_Splice_Rec_1919847,Human_Splice_Rec_1919851 RMVar_hsa_circ_118304,RMVar_hsa_circ_190454 91884 RMVar_ID_91884 Human_SNP_ID_263716006 m1A Human chr5 + 180071645 180071645 180071645 CGCGTTGTCTGCCCGTGCCGGCCACAGGCTGCAGGTCAGCAGGGCGAGCGCGGCGAGCCGGGCAG CGCGTTGTCTGCCCGTGCCGGCCACAGGCTGCGGGTCAGCAGGGCGAGCGCGGCGAGCCGGGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:180071606..180071703 26863196 MeRIP-seq:(Medium) rs1199726482 Functional Loss SNV dbSNP153 33..33 33 - - - 91885 RMVar_ID_91885 Human_SNP_ID_263716179 m1A Human chr5 - 180071887 180071887 180071887 CCCTCGCCGAGGGCCCATGGGCGCGTCCCCACAGGCGGGCAGTGGACGTGAGGGCGGCGAGCGGC CCCTCGCCGAGGGCCCATGGGCGCGTCCCCACGGGCGGGCAGTGGACGTGAGGGCGGCGAGCGGC T C RNF130 Ensembl:ENSG00000113269 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:180071837..180072102 26863196 MeRIP-seq:(Medium) rs1001062033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18046182 RMVar_hsa_circ_96706,RMVar_hsa_circ_236712 91886 RMVar_ID_91886 Human_SNP_ID_263743973 m1A Human chr5 - 180172875 180172875 180172875 GGATAGAGCATGGGCAAAGGCATGGAGGCGGGAGCACAGGGAGAGGCACAGGGAGGTGAGGAGCA GGATAGAGCATGGGCAAAGGCATGGAGGCGGGCGCACAGGGAGAGGCACAGGGAGGTGAGGAGCA T G RASGEF1C Ensembl:ENSG00000146090 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:180172735..180172920 26863196 MeRIP-seq:(Medium) rs1453492357 Functional Loss SNV dbSNP153 33..33 33 - - - 91887 RMVar_ID_91887 Human_SNP_ID_263754941 m1A Human chr5 + 180209154 180209125 180209154 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGACCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCG_____________________________CCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCGCCGCCGCCGCCGCCGCCCGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr5:180209081..180209187;chr5:180209032..180209220 26863196 MeRIP-seq:(Medium) rs1371957955 Functional Loss DEL dbSNP153 5..33 33 - - - 91888 RMVar_ID_91888 Human_SNP_ID_263754952 m1A Human chr5 + 180209154 180209131 180209154 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGACCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCG_______________________CCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCGCCGCCGCCGCCCGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr5:180209081..180209187;chr5:180209032..180209220 26863196 MeRIP-seq:(Medium) rs1181768730 Functional Loss DEL dbSNP153 11..33 33 - - - 91889 RMVar_ID_91889 Human_SNP_ID_263754958 m1A Human chr5 + 180209154 180209134 180209154 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGACCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCGCCG____________________CCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCGCCGCCGCCCGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr5:180209081..180209187;chr5:180209032..180209220 26863196 MeRIP-seq:(Medium) rs1183349103 Functional Loss DEL dbSNP153 14..33 33 - - - 91890 RMVar_ID_91890 Human_SNP_ID_263754968 m1A Human chr5 + 180209154 180209149 180209154 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGACCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCGCCGCCGCCGCCGCCGCCGCCGCCG_____CCGCCCGGCTCCCAGCGCAGCCCGCACGAGCG GCCCGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr5:180209081..180209187;chr5:180209032..180209220 26863196 MeRIP-seq:(Medium) rs1370787970 Functional Loss DEL dbSNP153 29..33 33 - - - 91891 RMVar_ID_91891 Human_SNP_ID_263773067 m1A Human chr5 + 180277362 180277360 180277362 GAGTCTGCTCCCTGCCTCTCTCAGCTGGTTGGAGGCTTCCTGTATTGCTTGGCTGTGGCCCCACA GAGTCTGCTCCCTGCCTCTCTCAGCTGGTTG__GGCTTCCTGTATTGCTTGGCTGTGGCCCCACA GGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:180277359..180277424 26863196 MeRIP-seq:(Medium) rs1463724780 Functional Loss DEL dbSNP153 32..33 33 - - - 91892 RMVar_ID_91892 Human_SNP_ID_263773951 m1A Human chr5 + 180280605 180280605 180280605 CTGCAATATCCCGAAGGGTGGGCAAGTTTCAGATCCCTTCAAAGAAAAACAGAATGAACGTGCAT CTGCAATATCCCGAAGGGTGGGCAAGTTTCAGTTCCCTTCAAAGAAAAACAGAATGAACGTGCAT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:180280551..180280625 26863196 MeRIP-seq:(Medium) rs1161944651 Functional Loss SNV dbSNP153 33..33 33 - - - 91893 RMVar_ID_91893 Human_SNP_ID_263776918 m1A Human chr5 - 180291854 180291854 180291854 GCCCGCCCTCTCCCCGTGGCGCGGCGGCGGGGAGGCGAGGTGAGCCCGGCGGGCGGGCTAGGCCT GCCCGCCCTCTCCCCGTGGCGCGGCGGCGGGGCGGCGAGGTGAGCCCGGCGGGCGGGCTAGGCCT T G MAPK9 Ensembl:ENSG00000050748 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:180291826..180292050 26863196 MeRIP-seq:(Medium) rs1293491947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846243,Human_RBP_ID_9335880,Human_RBP_ID_19127014,Human_RBP_ID_26792321 Human_Splice_Rec_730929,Human_Splice_Rec_730951,Human_Splice_Rec_730973,Human_Splice_Rec_730995,Human_Splice_Rec_731017,Human_Splice_Rec_731061,Human_Splice_Rec_731085,Human_Splice_Rec_731113 91894 RMVar_ID_91894 Human_SNP_ID_263776971 m1A Human chr5 - 180291965 180291965 180291965 CGGCGGCGGCGGCGGCGGCGGCGGCGGGGCGGAGCGGAGCGGGGCGGGCCGGCGGCGGAGCCGGG CGGCGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGCGGAGCGGGGCGGGCCGGCGGCGGAGCCGGG T C MAPK9 Ensembl:ENSG00000050748 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:180291851..180292050 26863410 MeRIP-seq:(Medium) rs1163495464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4827189,Human_RBP_ID_5327001,Human_RBP_ID_9335538 91895 RMVar_ID_91895 Human_SNP_ID_263777008 m1A Human chr5 + 180291999 180291993 180291999 CGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCCCCGCCGCCGCCGCCGCCGCCGCC______GTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCCGCA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr5:180291908..180292050;chr5:180291899..180292035 26863196,26863410 MeRIP-seq:(Medium) rs1561862615 Functional Loss DEL dbSNP153 28..33 33 - - - 91896 RMVar_ID_91896 Human_SNP_ID_263777011 m1A Human chr5 + 180291999 180291996 180291999 CGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCCCCGCCGCCGCCGCCGCCGCCGCCGCC___GTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr5:180291908..180292050;chr5:180291899..180292035 26863196,26863410 MeRIP-seq:(Medium) rs1290861290 Functional Loss DEL dbSNP153 31..33 33 - - - 91897 RMVar_ID_91897 Human_SNP_ID_263777013 m1A Human chr5 + 180291999 180291999 180291999 CGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr5:180291908..180292050;chr5:180291899..180292035 26863196,26863410 MeRIP-seq:(Medium) rs954215391 Functional Loss SNV dbSNP153 33..33 33 - - - 91898 RMVar_ID_91898 Human_SNP_ID_263777040 m1A Human chr5 - 180292025 180292025 180292025 GGCGGAGAAGGGAGCGGGACCGGAAGGGTCGCAGCGCCCCGGCGCCCCTCACACCCACTGCGGCG GGCGGAGAAGGGAGCGGGACCGGAAGGGTCGCTGCGCCCCGGCGCCCCTCACACCCACTGCGGCG T A MAPK9 Ensembl:ENSG00000050748 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:180291815..180292075;chr5:180280504..180292075 26863196 MeRIP-seq:(Medium) rs927368449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845569,Human_RBP_ID_9335538 91899 RMVar_ID_91899 Human_SNP_ID_263777043 m1A Human chr5 + 180292029 180292029 180292029 GCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACCCTTCCGGTCCCGCTCCCTTCTCCGCCGCTG GCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGGCCCTTCCGGTCCCGCTCCCTTCTCCGCCGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:180291826..180292050 26863196 MeRIP-seq:(Medium) rs1228254908 Functional Loss SNV dbSNP153 33..33 33 - - - 91900 RMVar_ID_91900 Human_SNP_ID_263777221 m1A Human chr5 - 180292383 180292383 180292383 CGCCTCCAGCCCGGTTCCCGGTCCTCCGGGCCACCCTCTCCACCGAGCTGCGCCCCCCTCGCAGG CGCCTCCAGCCCGGTTCCCGGTCCTCCGGGCCGCCCTCTCCACCGAGCTGCGCCCCCCTCGCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180292186..180292929 26863196 MeRIP-seq:(Medium) rs887122407 Functional Loss SNV dbSNP153 33..33 33 - - - 91901 RMVar_ID_91901 Human_SNP_ID_263777329 m1A Human chr5 + 180292698 180292698 180292698 AGAAGCCGGGTCGAAGAGGGGGAGGGGGTGCGAAGAGATGGCGGTGTGTAGACAGGTGACCCGGT AGAAGCCGGGTCGAAGAGGGGGAGGGGGTGCGGAGAGATGGCGGTGTGTAGACAGGTGACCCGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:180292209..180292931 26863196 MeRIP-seq:(Medium) rs10214064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24101214 91902 RMVar_ID_91902 Human_SNP_ID_263777555 m1A Human chr5 - 180293321 180293321 180293321 GTGCCCAGCCTCAGTGCCTCTCTTCCTGCTTCACTTTTCAACGTAGATCTGGCAACATCCCAAGC GTGCCCAGCCTCAGTGCCTCTCTTCCTGCTTCGCTTTTCAACGTAGATCTGGCAACATCCCAAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:180293203..180293652 26863196 MeRIP-seq:(Medium) rs1164685922 Functional Loss SNV dbSNP153 33..33 33 - - - 91903 RMVar_ID_91903 Human_SNP_ID_263777560 m1A Human chr5 + 180293333 180293333 180293333 GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGAGAGGCACTGAGGCTGGGCACATGGGGAAAACC GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGGGAGGCACTGAGGCTGGGCACATGGGGAAAACC A G AC008610.1 Ensembl:ENSG00000248367 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180293282..180293556 26863196 MeRIP-seq:(Medium) rs75469971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5615028 Human_Splice_Rec_731121 91904 RMVar_ID_91904 Human_SNP_ID_263777561 m1A Human chr5 + 180293333 180293333 180293333 GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGAGAGGCACTGAGGCTGGGCACATGGGGAAAACC GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGTGAGGCACTGAGGCTGGGCACATGGGGAAAACC A T AC008610.1 Ensembl:ENSG00000248367 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180293282..180293556 26863196 MeRIP-seq:(Medium) rs75469971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5615028 Human_Splice_Rec_731121 91905 RMVar_ID_91905 Human_SNP_ID_263777678 m1A Human chr5 - 180293808 180293808 180293808 TTTCTGGTTTCCTGTTCTCTCTCATGCACTTGAGGCAGGTGGCAGGTGAGTCTGAGGTAGCGACA TTTCTGGTTTCCTGTTCTCTCTCATGCACTTGGGGCAGGTGGCAGGTGAGTCTGAGGTAGCGACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:180293798..180293876 26863196 MeRIP-seq:(Medium) rs1019570893 Functional Loss SNV dbSNP153 33..33 33 - - - 91906 RMVar_ID_91906 Human_SNP_ID_263795629 m1A Human chr5 - 180353291 180353289 180353292 GGAGCCCACGGAGCCCACGGAGCCCACGGAGGAGCCCACGGAGGAGCCCCAGCGTCCGAACGGGC GGAGCCCACGGAGCCCACGGAGCCCACGGAG___CCCACGGAGGAGCCCCAGCGTCCGAACGGGC GCTC G GFPT2 Ensembl:ENSG00000131459 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180353242..180353313 26863196 MeRIP-seq:(Medium) rs145699272 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_731123,Human_Splice_Rec_731181,Human_Splice_Rec_731189 91907 RMVar_ID_91907 Human_SNP_ID_263822015 m1A Human chr5 - 180441833 180441833 180441833 CCACACTCACCTCTCCAGGCACCCCGCTGGCCAGGCCCCAGCGCGCATGCCTTCACGCGGCTGTA CCACACTCACCTCTCCAGGCACCCCGCTGGCCGGGCCCCAGCGCGCATGCCTTCACGCGGCTGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180441785..180441869 26863196 MeRIP-seq:(Medium) rs527967477 Functional Loss SNV dbSNP153 33..33 33 - - - 91908 RMVar_ID_91908 Human_SNP_ID_263829202 m1A Human chr5 - 180469281 180469279 180469282 CCCCCGCCCCCCAACCCAGGGAACTGCACACCACACCTGCTCGCTTCTGCCAGAAGCCTGAGCAG CCCCCGCCCCCCAACCCAGGGAACTGCACAC___ACCTGCTCGCTTCTGCCAGAAGCCTGAGCAG TGTG T lnc-SCGB3A1-3,lnc-SCGB3A1-3:2,lnc-SCGB3A1-3:3 RNACentral:URS0000D5E247,RNACentral:URS0000D5D972,RNACentral:URS0000D587DE lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:180469231..180469379 26863196 MeRIP-seq:(Medium) rs1220921515 Functional Loss DEL dbSNP153 32..34 33 - - - 91909 RMVar_ID_91909 Human_SNP_ID_263833693 m1A Human chr5 - 180486503 180486503 180486503 ATACCGTTGCTGGAAGAAAGAGGAATAGAAGCAGCAAGGAAGAAAGGCAGAGGCCTGAGGTCCAC ATACCGTTGCTGGAAGAAAGAGGAATAGAAGCGGCAAGGAAGAAAGGCAGAGGCCTGAGGTCCAC T C lnc-SCGB3A1-3,lnc-SCGB3A1-3:2,lnc-SCGB3A1-3:3,lnc-SCGB3A1-3:4,lnc-SCGB3A1-3:5,lnc-SCGB3A1-3:6,lnc-SCGB3A1-3:7,lnc-SCGB3A1-3:8 RNACentral:URS0000D5BF15,RNACentral:URS0000D56DA5,RNACentral:URS0000D5AE3D,RNACentral:URS0000D5CBD7,RNACentral:URS0000D5E247,RNACentral:URS0000D5D972,RNACentral:URS0000D5A1EB,RNACentral:URS0000D587DE lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron,intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:180486464..180486548 26863196 MeRIP-seq:(Medium) rs1349265154 Functional Loss SNV dbSNP153 33..33 33 - - - 91910 RMVar_ID_91910 Human_SNP_ID_263835892 m1A Human chr5 + 180494446 180494446 180494446 TTTCAATGAAAACGAGGGGGGCGCGGAGGAGGAGGCGGCGGCGTCGGTGGCGGCGGCGACGGCGG TTTCAATGAAAACGAGGGGGGCGCGGAGGAGGCGGCGGCGGCGTCGGTGGCGGCGGCGACGGCGG A C CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:180494395..180494725 26863196 MeRIP-seq:(Medium) rs1233413406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_4827233,Human_RBP_ID_9335539,Human_RBP_ID_18425238 91911 RMVar_ID_91911 Human_SNP_ID_263835897 m1A Human chr5 + 180494472 180494448 180494472 AGGAGGAGGCGGCGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG AGGAGGAGG________________________CGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG GCGGCGGCGTCGGTGGCGGCGGCGA G CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180494351..180494806 26863196 MeRIP-seq:(Medium) rs1443969535 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_4827233,Human_RBP_ID_9335539,Human_RBP_ID_18425238 91912 RMVar_ID_91912 Human_SNP_ID_263835910 m1A Human chr5 + 180494484 180494461 180494484 CGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG CGGCGTCGGT_______________________GGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG TGGCGGCGGCGACGGCGGCGCGGA T CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr5:180494401..180494749;chr5:180494433..180494524 26863196,26863410 MeRIP-seq:(Medium) rs1334025051 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_18425238 91913 RMVar_ID_91913 Human_SNP_ID_263835915 m1A Human chr5 + 180494472 180494463 180494472 AGGAGGAGGCGGCGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG AGGAGGAGGCGGCGGCGTCGGTGG_________CGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG GCGGCGGCGA G CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180494351..180494806 26863196 MeRIP-seq:(Medium) rs1309965304 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_4827233,Human_RBP_ID_9335539,Human_RBP_ID_18425238 91914 RMVar_ID_91914 Human_SNP_ID_263835921 m1A Human chr5 + 180494472 180494472 180494472 AGGAGGAGGCGGCGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG AGGAGGAGGCGGCGGCGTCGGTGGCGGCGGCGGCGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCG A G CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180494351..180494806 26863196 MeRIP-seq:(Medium) rs1461406774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_4827233,Human_RBP_ID_9335539,Human_RBP_ID_18425238 91915 RMVar_ID_91915 Human_SNP_ID_263835925 m1A Human chr5 + 180494484 180494476 180494484 CGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG CGGCGTCGGTGGCGGCGGCGACGGC________GGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG CGGCGCGGA C CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr5:180494401..180494749;chr5:180494433..180494524 26863196,26863410 MeRIP-seq:(Medium) rs912751790 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_18425238 91916 RMVar_ID_91916 Human_SNP_ID_263835930 m1A Human chr5 + 180494484 180494484 180494484 CGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGAGGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG CGGCGTCGGTGGCGGCGGCGACGGCGGCGCGGGGGCGAAGGCAGCGGCGGGCGCAGCGAGGAGGG A G CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T cell line,total RNA;HEK293T,Starvation treatment chr5:180494401..180494749;chr5:180494433..180494524 26863196,26863410 MeRIP-seq:(Medium) rs1411499951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_18425238 91917 RMVar_ID_91917 Human_SNP_ID_263835952 m1A Human chr5 + 180494532 180494532 180494532 GGGCGCAGCGAGGAGGGCGAGGCCGGGGGCCGAGAGGGCGGGAGGGCGTAGTGGCGGCCCGTCGG GGGCGCAGCGAGGAGGGCGAGGCCGGGGGCCGGGAGGGCGGGAGGGCGTAGTGGCGGCCCGTCGG A G CNOT6 Ensembl:ENSG00000113300 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:180494450..180494537 26863410 MeRIP-seq:(Medium) rs1395863203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788616,Human_RBP_ID_5326695,Human_RBP_ID_9436639,Human_RBP_ID_18425239,Human_RBP_ID_26792322,Human_RBP_ID_27842166 91918 RMVar_ID_91918 Human_SNP_ID_263836370 m1A Human chr5 - 180495569 180495569 180495569 CACATCAGCTTACACAGTAACAACAAATCCAAAGAGCTCGAGCGAGATGACCATTCACAACGCTG CACATCAGCTTACACAGTAACAACAAATCCAAGGAGCTCGAGCGAGATGACCATTCACAACGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:180495567..180529400 26863196 MeRIP-seq:(Medium) rs1411878139 Functional Loss SNV dbSNP153 33..33 33 - - - 91919 RMVar_ID_91919 Human_SNP_ID_263845474 m1A Human chr5 + 180529213 180529212 180529214 GAGTCAGACTTCGTCTCAAAAAAAAAAAAAAAAGGTGTTGTGGCTTTTGTTTATTTGATTTTTTA GAGTCAGACTTCGTCTCAAAAAAAAAAAAAAA__GTGTTGTGGCTTTTGTTTATTTGATTTTTTA AAG A CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:180529211..180549941 26863196 MeRIP-seq:(Medium) rs34869750 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_33719,RMVar_hsa_circ_78985,RMVar_hsa_circ_50416,RMVar_hsa_circ_236743,RMVar_hsa_circ_236744,RMVar_hsa_circ_20569,RMVar_hsa_circ_236745 91920 RMVar_ID_91920 Human_SNP_ID_263858375 m1A Human chr5 - 180574113 180574113 180574113 AGCTCCAGTTGTGCAAAAAGTGAGAAGTGGTCAGAGGGGATGAGGGGGTGCGGGCAGCCACTGAT AGCTCCAGTTGTGCAAAAAGTGAGAAGTGGTCGGAGGGGATGAGGGGGTGCGGGCAGCCACTGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180574063..180574164 26863196 MeRIP-seq:(Medium) rs757061996 Functional Loss SNV dbSNP153 33..33 33 - - - 91921 RMVar_ID_91921 Human_SNP_ID_263919396 m1A Human chr5 - 180790761 180790761 180790761 TTGACACACAGGCTCCTCTCAGCATGAGGTGGAGCAGTGACCAGGTGGAGCAGTGACCAGGACGC TTGACACACAGGCTCCTCTCAGCATGAGGTGGTGCAGTGACCAGGTGGAGCAGTGACCAGGACGC T A MGAT1 Ensembl:ENSG00000131446 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:180790618..180791418 32194978 MeRIP-seq:(Medium) rs941363172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640467,Human_RBP_ID_787829,Human_RBP_ID_1041074,Human_RBP_ID_7425544,Human_RBP_ID_18840529,Human_RBP_ID_26529614 RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 91922 RMVar_ID_91922 Human_SNP_ID_263919436 m1A Human chr5 + 180790923 180790923 180790923 GGAGGGGTCAGGGCATAGTCCCTCTCTGAGGTAAGGCAAGAGAGAGGTTGTCCCAGCACAAGGCC GGAGGGGTCAGGGCATAGTCCCTCTCTGAGGTGAGGCAAGAGAGAGGTTGTCCCAGCACAAGGCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:180790901..180790925 32194978 MeRIP-seq:(Medium) rs1192045549 Functional Loss SNV dbSNP153 33..33 33 - - - 91923 RMVar_ID_91923 Human_SNP_ID_263919697 m1A Human chr5 - 180791670 180791670 180791670 TTCCGGGGCCGCCGTGTCCACCTGGCGCCCCCACTGACGTGGGAGGGCTATGATCCTAGCTGGAA TTCCGGGGCCGCCGTGTCCACCTGGCGCCCCCGCTGACGTGGGAGGGCTATGATCCTAGCTGGAA T C MGAT1 Ensembl:ENSG00000131446 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:180791626..180791800 32194978 MeRIP-seq:(Medium) rs1428309449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18195190,Human_RBP_ID_22100758,Human_RBP_ID_22459454,Human_RBP_ID_22772230,Human_RBP_ID_26826953 Human_miRNA_ID_2867531 RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 91924 RMVar_ID_91924 Human_SNP_ID_263921124 m1A Human chr5 - 180795798 180795797 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCA_TTTGCCTTGCTGATGTGCCAGCTGGGATTACG AT A MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs143541561 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9175517 Human_Splice_Rec_731658,Human_Splice_Rec_731678,Human_Splice_Rec_731688,Human_Splice_Rec_731690 RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 91925 RMVar_ID_91925 Human_SNP_ID_263921125 m1A Human chr5 - 180795798 180795798 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCAGTTTGCCTTGCTGATGTGCCAGCTGGGATTACG T C MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs187620094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9175517 Human_Splice_Rec_731658,Human_Splice_Rec_731678,Human_Splice_Rec_731688,Human_Splice_Rec_731690 RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 91926 RMVar_ID_91926 Human_SNP_ID_263924871 m1A Human chr5 - 180809064 180809064 180809064 AATGTTTAAATGTTCTGCAGGTTAACACAGAAATCTGCCTCCTGGGCCATGCCGCTTCTAAGGCC AATGTTTAAATGTTCTGCAGGTTAACACAGAAGTCTGCCTCCTGGGCCATGCCGCTTCTAAGGCC T C MGAT1 Ensembl:ENSG00000131446 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:180809015..180809115 26863196 MeRIP-seq:(Medium) rs930379222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846249,Human_RBP_ID_18840542,Human_RBP_ID_22512219 Human_Splice_Rec_731642,Human_Splice_Rec_731648,Human_Splice_Rec_731652,Human_Splice_Rec_731662,Human_Splice_Rec_731682,Human_Splice_Rec_731692,Human_Splice_Rec_731696,Human_Splice_Rec_731698,Human_Splice_Rec_731700,Human_Splice_Rec_731702,Human_Splice_Rec_731704,Human_Splice_Rec_731706 Human_miRNA_ID_2474773,Human_miRNA_ID_2492697,Human_miRNA_ID_2960560,Human_miRNA_ID_2992578 RMVar_hsa_circ_236771,RMVar_hsa_circ_374657 91927 RMVar_ID_91927 Human_SNP_ID_263936858 m1A Human chr5 - 180851241 180851241 180851241 AGCCAAGAGTACAGCAAATATAAAGACAGAACAGGAAGGTGAGGCATCTGAGAAGAGCTTGCATC AGCCAAGAGTACAGCAAATATAAAGACAGAACGGGAAGGTGAGGCATCTGAGAAGAGCTTGCATC T C ZFP62 Ensembl:ENSG00000196670 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180851190..180851300 26863196 MeRIP-seq:(Medium) rs1342228470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640541,Human_RBP_ID_1660411,Human_RBP_ID_4854189,Human_RBP_ID_7425688,Human_RBP_ID_22527662,Human_RBP_ID_24548164 91928 RMVar_ID_91928 Human_SNP_ID_263939563 m1A Human chr5 - 180860999 180860999 180860999 GCAGAGGGGTGCAGGGCGCGCCCCTGGAACAGACTGGGCTCTGTGTGGGCCACAACTGCGACGTT GCAGAGGGGTGCAGGGCGCGCCCCTGGAACAGGCTGGGCTCTGTGTGGGCCACAACTGCGACGTT T C ZFP62 Ensembl:ENSG00000196670 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr5:180860957..180861083;chr5:180860881..180861084 26863196 MeRIP-seq:(Medium) rs936029377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250988,Human_RBP_ID_15416545,Human_RBP_ID_17707926,Human_RBP_ID_21900884 91929 RMVar_ID_91929 Human_SNP_ID_264016457 m1A Human chr5 - 181174059 181174059 181174059 AAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGAATCCCACCGCTGCCAGCTTGTTGTGGTTTGCC AAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGTATCCCACCGCTGCCAGCTTGTTGTGGTTTGCC T A tRNA-Leu-AAG-1-1 RNACentral:URS0000630B8A tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1232809619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640584,Human_RBP_ID_21158980,Human_RBP_ID_24101829,Human_RBP_ID_27085703 91930 RMVar_ID_91930 Human_SNP_ID_264016458 m1A Human chr5 - 181174059 181174059 181174059 AAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGAATCCCACCGCTGCCAGCTTGTTGTGGTTTGCC AAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGGATCCCACCGCTGCCAGCTTGTTGTGGTTTGCC T C tRNA-Leu-AAG-1-1 RNACentral:URS0000630B8A tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1232809619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640584,Human_RBP_ID_21158980,Human_RBP_ID_24101829,Human_RBP_ID_27085703 91931 RMVar_ID_91931 Human_SNP_ID_264020598 m1A Human chr5 + 181187767 181187767 181187767 AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGAATCCCACCGCTGCCAGTTTGTGGTAGTTTTGT AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGGATCCCACCGCTGCCAGTTTGTGGTAGTTTTGT A G RF00017-049,tRNA-Leu-AAG-2-3 RNACentral:URS000096B6E3,RNACentral:URS0000120E41 SRP RNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1332200953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640586,Human_RBP_ID_1652835,Human_RBP_ID_5276522,Human_RBP_ID_5509447,Human_RBP_ID_8612883,Human_RBP_ID_10199660,Human_RBP_ID_18840621,Human_RBP_ID_21158985,Human_RBP_ID_22828262,Human_RBP_ID_23136936,Human_RBP_ID_24101832,Human_RBP_ID_24434460,Human_RBP_ID_27080758 91932 RMVar_ID_91932 Human_SNP_ID_264021052 m1A Human chr5 - 181188445 181188445 181188445 GTAGTGGTCATCACGTTCGCCTAACACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACATGC GTAGTGGTCATCACGTTCGCCTAACACGCGAATGGTCCCCGGTTCGAAACCGGGCGGAAACATGC T A LINC01962 Ensembl:ENSG00000248473 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181188439..181188607 26863196 MeRIP-seq:(Medium) rs901643629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284067,Human_RBP_ID_640588,Human_RBP_ID_1041097,Human_RBP_ID_1212356,Human_RBP_ID_1244569,Human_RBP_ID_1321109,Human_RBP_ID_1391284,Human_RBP_ID_1660928,Human_RBP_ID_1993908,Human_RBP_ID_2922436,Human_RBP_ID_3767465,Human_RBP_ID_4827909,Human_RBP_ID_5104133,Human_RBP_ID_5212747,Human_RBP_ID_5250826,Human_RBP_ID_5267295,Human_RBP_ID_5276524,Human_RBP_ID_5427642,Human_RBP_ID_5449738,Human_RBP_ID_5476618,Human_RBP_ID_5509448,Human_RBP_ID_5610761,Human_RBP_ID_7425802,Human_RBP_ID_8137633,Human_RBP_ID_8267510,Human_RBP_ID_8612886,Human_RBP_ID_8894647,Human_RBP_ID_9175537,Human_RBP_ID_9305593,Human_RBP_ID_15416745,Human_RBP_ID_17038146,Human_RBP_ID_17090689,Human_RBP_ID_17417372,Human_RBP_ID_17529576,Human_RBP_ID_17707932,Human_RBP_ID_18046473,Human_RBP_ID_18202344,Human_RBP_ID_18210523,Human_RBP_ID_18448664,Human_RBP_ID_18840625,Human_RBP_ID_21087966,Human_RBP_ID_22512224,Human_RBP_ID_22828263,Human_RBP_ID_23136938,Human_RBP_ID_23291507,Human_RBP_ID_23314013,Human_RBP_ID_24124877,Human_RBP_ID_24536001,Human_RBP_ID_24540509,Human_RBP_ID_26701988,Human_RBP_ID_26751198,Human_RBP_ID_27080759,Human_RBP_ID_27160675,Human_RBP_ID_27335960,Human_RBP_ID_27518266,Human_RBP_ID_27567532,Human_RBP_ID_27739455 91933 RMVar_ID_91933 Human_SNP_ID_264021053 m1A Human chr5 - 181188445 181188445 181188445 GTAGTGGTCATCACGTTCGCCTAACACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACATGC GTAGTGGTCATCACGTTCGCCTAACACGCGAAGGGTCCCCGGTTCGAAACCGGGCGGAAACATGC T C LINC01962 Ensembl:ENSG00000248473 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181188439..181188607 26863196 MeRIP-seq:(Medium) rs901643629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284067,Human_RBP_ID_640588,Human_RBP_ID_1041097,Human_RBP_ID_1212356,Human_RBP_ID_1244569,Human_RBP_ID_1321109,Human_RBP_ID_1391284,Human_RBP_ID_1660928,Human_RBP_ID_1993908,Human_RBP_ID_2922436,Human_RBP_ID_3767465,Human_RBP_ID_4827909,Human_RBP_ID_5104133,Human_RBP_ID_5212747,Human_RBP_ID_5250826,Human_RBP_ID_5267295,Human_RBP_ID_5276524,Human_RBP_ID_5427642,Human_RBP_ID_5449738,Human_RBP_ID_5476618,Human_RBP_ID_5509448,Human_RBP_ID_5610761,Human_RBP_ID_7425802,Human_RBP_ID_8137633,Human_RBP_ID_8267510,Human_RBP_ID_8612886,Human_RBP_ID_8894647,Human_RBP_ID_9175537,Human_RBP_ID_9305593,Human_RBP_ID_15416745,Human_RBP_ID_17038146,Human_RBP_ID_17090689,Human_RBP_ID_17417372,Human_RBP_ID_17529576,Human_RBP_ID_17707932,Human_RBP_ID_18046473,Human_RBP_ID_18202344,Human_RBP_ID_18210523,Human_RBP_ID_18448664,Human_RBP_ID_18840625,Human_RBP_ID_21087966,Human_RBP_ID_22512224,Human_RBP_ID_22828263,Human_RBP_ID_23136938,Human_RBP_ID_23291507,Human_RBP_ID_23314013,Human_RBP_ID_24124877,Human_RBP_ID_24536001,Human_RBP_ID_24540509,Human_RBP_ID_26701988,Human_RBP_ID_26751198,Human_RBP_ID_27080759,Human_RBP_ID_27160675,Human_RBP_ID_27335960,Human_RBP_ID_27518266,Human_RBP_ID_27567532,Human_RBP_ID_27739455 91934 RMVar_ID_91934 Human_SNP_ID_264021161 m1A Human chr5 + 181188509 181188509 181188509 CACTACGGAAACCCACACCTACCTCTGTCGCCATAATATTGTCTGCTAGCAGCTACTCTCCGGGT CACTACGGAAACCCACACCTACCTCTGTCGCCCTAATATTGTCTGCTAGCAGCTACTCTCCGGGT A C RF00017-049,lnc-OR2V2-3 RNACentral:URS000096B6E3,RNACentral:URS00008B9BC2 SRP RNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181188462..181188573 26863196 MeRIP-seq:(Medium) rs73357352 Functional Loss SNV dbSNP153 33..33 33 - - - 91935 RMVar_ID_91935 Human_SNP_ID_264021162 m1A Human chr5 + 181188509 181188509 181188509 CACTACGGAAACCCACACCTACCTCTGTCGCCATAATATTGTCTGCTAGCAGCTACTCTCCGGGT CACTACGGAAACCCACACCTACCTCTGTCGCCGTAATATTGTCTGCTAGCAGCTACTCTCCGGGT A G RF00017-049,lnc-OR2V2-3 RNACentral:URS000096B6E3,RNACentral:URS00008B9BC2 SRP RNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181188462..181188573 26863196 MeRIP-seq:(Medium) rs73357352 Functional Loss SNV dbSNP153 33..33 33 - - - 91936 RMVar_ID_91936 Human_SNP_ID_264022273 m1A Human chr5 + 181191669 181191669 181191669 CTATCTTCCACTTTTCTATCTTTAAGGAAAGAATAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT CTATCTTCCACTTTTCTATCTTTAAGGAAAGACTAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT A C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181191618..181191690 26863196 MeRIP-seq:(Medium) rs952816187 Functional Loss SNV dbSNP153 33..33 33 - - - 91937 RMVar_ID_91937 Human_SNP_ID_264022274 m1A Human chr5 + 181191669 181191669 181191669 CTATCTTCCACTTTTCTATCTTTAAGGAAAGAATAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT CTATCTTCCACTTTTCTATCTTTAAGGAAAGAGTAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181191618..181191690 26863196 MeRIP-seq:(Medium) rs952816187 Functional Loss SNV dbSNP153 33..33 33 - - - 91938 RMVar_ID_91938 Human_SNP_ID_264022275 m1A Human chr5 + 181191669 181191669 181191669 CTATCTTCCACTTTTCTATCTTTAAGGAAAGAATAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT CTATCTTCCACTTTTCTATCTTTAAGGAAAGATTAGGAAAAGACGGAAGCAGGCCCCAGCGAGAT A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181191618..181191690 26863196 MeRIP-seq:(Medium) rs952816187 Functional Loss SNV dbSNP153 33..33 33 - - - 91939 RMVar_ID_91939 Human_SNP_ID_264022320 m1A Human chr5 - 181191702 181191702 181191702 CACTGGTCTTGTAAACCAGGGTCGCGAGTTCAAATCTCGCTGGGGCCTGCTTCCGTCTTTTCCTA CACTGGTCTTGTAAACCAGGGTCGCGAGTTCACATCTCGCTGGGGCCTGCTTCCGTCTTTTCCTA T G LINC01962 Ensembl:ENSG00000248473 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1282084407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251028,Human_RBP_ID_789328,Human_RBP_ID_838764,Human_RBP_ID_1660605,Human_RBP_ID_3784485,Human_RBP_ID_4847294,Human_RBP_ID_5090172,Human_RBP_ID_5213962,Human_RBP_ID_5250785,Human_RBP_ID_5267728,Human_RBP_ID_5427215,Human_RBP_ID_5656137,Human_RBP_ID_7425814,Human_RBP_ID_8215023,Human_RBP_ID_8267520,Human_RBP_ID_8612894,Human_RBP_ID_8889154,Human_RBP_ID_10199665,Human_RBP_ID_15416762,Human_RBP_ID_17157916,Human_RBP_ID_17529579,Human_RBP_ID_18046479,Human_RBP_ID_18448665,Human_RBP_ID_18545620,Human_RBP_ID_18840635,Human_RBP_ID_21218216,Human_RBP_ID_22009769,Human_RBP_ID_22098121,Human_RBP_ID_22300218,Human_RBP_ID_22829111,Human_RBP_ID_23136953,Human_RBP_ID_24101839,Human_RBP_ID_24509004,Human_RBP_ID_24554473,Human_RBP_ID_25887207,Human_RBP_ID_27080765,Human_RBP_ID_27335969,Human_RBP_ID_27515176 91940 RMVar_ID_91940 Human_SNP_ID_264022517 m1A Human chr5 - 181191958 181191958 181191958 GCCCCGACAGCTCCCGCCCGCGCGCGCGCCCAACGACGGCACTGTCTTCGCGGAGCCCTCTGCCG GCCCCGACAGCTCCCGCCCGCGCGCGCGCCCAGCGACGGCACTGTCTTCGCGGAGCCCTCTGCCG T C LINC01962 RNACentral:URS00008B7AAE lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181191917..181193372 26863196 MeRIP-seq:(Medium) rs1338436849 Functional Loss SNV dbSNP153 33..33 33 - - - 91941 RMVar_ID_91941 Human_SNP_ID_264025844 m1A Human chr5 + 181203517 181203517 181203517 GGTGCTGAGTTCTCAGGCCTCTGTAATGTCCCACGGGGGGCCTGCGGGTGCCTGGCTCACCAGCA GGTGCTGAGTTCTCAGGCCTCTGTAATGTCCCTCGGGGGGCCTGCGGGTGCCTGGCTCACCAGCA A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181203469..181203599 26863196 MeRIP-seq:(Medium) rs767136388 Functional Loss SNV dbSNP153 33..33 33 - - - 91942 RMVar_ID_91942 Human_SNP_ID_264026289 m1A Human chr5 + 181204778 181204778 181204778 GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCAGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCGGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181204727..181204831 26863196 MeRIP-seq:(Medium) rs2770944 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 91943 RMVar_ID_91943 Human_SNP_ID_264026290 m1A Human chr5 + 181204778 181204778 181204778 GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCAGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCTGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181204727..181204831 26863196 MeRIP-seq:(Medium) rs2770944 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 91944 RMVar_ID_91944 Human_SNP_ID_264031078 m1A Human chr5 + 181218229 181218229 181218229 AAAACTTGTGAACGTTTATACACATAGACTCCACACTAAGAAACCTTTTTGAACTGGAAGGAAAA AAAACTTGTGAACGTTTATACACATAGACTCCCCACTAAGAAACCTTTTTGAACTGGAAGGAAAA A C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181218085..181218289 26863196 MeRIP-seq:(Medium) rs191796939 Functional Loss SNV dbSNP153 33..33 33 - - - 91945 RMVar_ID_91945 Human_SNP_ID_264031079 m1A Human chr5 + 181218229 181218229 181218229 AAAACTTGTGAACGTTTATACACATAGACTCCACACTAAGAAACCTTTTTGAACTGGAAGGAAAA AAAACTTGTGAACGTTTATACACATAGACTCCGCACTAAGAAACCTTTTTGAACTGGAAGGAAAA A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181218085..181218289 26863196 MeRIP-seq:(Medium) rs191796939 Functional Loss SNV dbSNP153 33..33 33 - - - 91946 RMVar_ID_91946 Human_SNP_ID_264031094 m1A Human chr5 - 181218251 181218251 181218251 ACCGGGCGGAAACAAGACTGTGTTTTCCTTCCAGTTCAAAAAGGTTTCTTAGTGTGGAGTCTATG ACCGGGCGGAAACAAGACTGTGTTTTCCTTCCCGTTCAAAAAGGTTTCTTAGTGTGGAGTCTATG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181218097..181218308 26863196 MeRIP-seq:(Medium) rs1236615270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1652851,Human_RBP_ID_1993920,Human_RBP_ID_5216028,Human_RBP_ID_5276415,Human_RBP_ID_8612916,Human_RBP_ID_18046492,Human_RBP_ID_22828275,Human_RBP_ID_23136980,Human_RBP_ID_24432610 91947 RMVar_ID_91947 Human_SNP_ID_264033183 m1A Human chr5 - 181223398 181223397 181223398 TCCCCCGCCGCTGGGGAGAAACTTCGGGGGGTAGGGGGAGCGCCTGGCGGCCGTCTGCTTTCGGT TCCCCCGCCGCTGGGGAGAAACTTCGGGGGGT_GGGGGAGCGCCTGGCGGCCGTCTGCTTTCGGT CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181223355..181223605 32194978 MeRIP-seq:(Medium) rs1218957273 Functional Loss DEL dbSNP153 33..33 33 - - - 91948 RMVar_ID_91948 Human_SNP_ID_264033448 m1A Human chr5 + 181224036 181224036 181224036 CTGCCGTTGCCATGACACCCAACCCTGTGCAGACCCTTCAGGAGGAGGCGGTGTGCGCCATCTGC CTGCCGTTGCCATGACACCCAACCCTGTGCAGTCCCTTCAGGAGGAGGCGGTGTGCGCCATCTGC A T TRIM41 Ensembl:ENSG00000146063 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181223703..181224153 32194978 MeRIP-seq:(Medium) rs1364486491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18840666 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 91949 RMVar_ID_91949 Human_SNP_ID_264033567 m1A Human chr5 + 181224308 181224308 181224308 GGTGACATGGAGGAGGAGGTCGAGGAGGAAGAAGAGGGTGTGTTCTGGACCAGTGGCATGAGCAG GGTGACATGGAGGAGGAGGTCGAGGAGGAAGACGAGGGTGTGTTCTGGACCAGTGGCATGAGCAG A C TRIM41 Ensembl:ENSG00000146063 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181223301..181224700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_12850,Human_RBP_ID_840031,Human_RBP_ID_3783026,Human_RBP_ID_3967711,Human_RBP_ID_5151229,Human_RBP_ID_5213706,Human_RBP_ID_5327010,Human_RBP_ID_5532141,Human_RBP_ID_7425854,Human_RBP_ID_8213349,Human_RBP_ID_8612931,Human_RBP_ID_8889165,Human_RBP_ID_9335888,Human_RBP_ID_9349764,Human_RBP_ID_9436643,Human_RBP_ID_15416815,Human_RBP_ID_19125158,Human_RBP_ID_22099937,Human_RBP_ID_23120179,Human_RBP_ID_24101865,Human_RBP_ID_26351924,Human_RBP_ID_26529625,Human_RBP_ID_27826192 Human_miRNA_ID_946745,Human_miRNA_ID_1054717,Human_miRNA_ID_2428483,Human_miRNA_ID_2428484,Human_miRNA_ID_2488283,Human_miRNA_ID_2488284 RMVar_hsa_circ_114296,RMVar_hsa_circ_236775,RMVar_hsa_circ_236774,RMVar_hsa_circ_377793 91950 RMVar_ID_91950 Human_SNP_ID_264033618 m1A Human chr5 - 181224446 181224422 181224446 ACCTCCTCCAGCACTTCCTCCTCGTCCTCCTCATCCTCCCCCCTCAGGTCCTCCTCCTCCATGTC ACCTCCTCCAGCACTTCCTCCTCGTCCTCCTC________________________CTCCATGTC GGAGGAGGACCTGAGGGGGGAGGAT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181224351..181224452 32194978 MeRIP-seq:(Medium) rs766909473 Functional Loss DEL dbSNP153 33..56 33 - - - 91951 RMVar_ID_91951 Human_SNP_ID_264033638 m1A Human chr5 - 181224446 181224446 181224446 ACCTCCTCCAGCACTTCCTCCTCGTCCTCCTCATCCTCCCCCCTCAGGTCCTCCTCCTCCATGTC ACCTCCTCCAGCACTTCCTCCTCGTCCTCCTCCTCCTCCCCCCTCAGGTCCTCCTCCTCCATGTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181224351..181224452 32194978 MeRIP-seq:(Medium) rs756209066 Functional Loss SNV dbSNP153 33..33 33 - - - 91952 RMVar_ID_91952 Human_SNP_ID_264035965 m1A Human chr5 + 181232325 181232325 181232325 CAATATTATATGTGCCACAGAGAGATACAGTGATATTTGTGGGGATGGTCCCGATTTAGATCTGG CAATATTATATGTGCCACAGAGAGATACAGTGGTATTTGTGGGGATGGTCCCGATTTAGATCTGG A G TRIM41 Ensembl:ENSG00000146063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181232321..181232479 26863196 MeRIP-seq:(Medium) rs1478901754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27739465 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 91953 RMVar_ID_91953 Human_SNP_ID_264036458 m1A Human chr5 - 181233743 181233743 181233743 TGACCTCCCTACCTCTCGCAGCCTGACAGAACATCCGGCTCATTTTCCTCACGATGGCATCTGTC TGACCTCCCTACCTCTCGCAGCCTGACAGAACGTCCGGCTCATTTTCCTCACGATGGCATCTGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181233367..181233755 26863196 MeRIP-seq:(Medium) rs1350465170 Functional Loss SNV dbSNP153 33..33 33 - - - 91954 RMVar_ID_91954 Human_SNP_ID_264036459 m1A Human chr5 - 181233743 181233743 181233743 TGACCTCCCTACCTCTCGCAGCCTGACAGAACATCCGGCTCATTTTCCTCACGATGGCATCTGTC TGACCTCCCTACCTCTCGCAGCCTGACAGAACCTCCGGCTCATTTTCCTCACGATGGCATCTGTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181233367..181233755 26863196 MeRIP-seq:(Medium) rs1350465170 Functional Loss SNV dbSNP153 33..33 33 - - - 91955 RMVar_ID_91955 Human_SNP_ID_264036618 m1A Human chr5 + 181234197 181234197 181234197 CCTCCCAAGTGGACCTGACGCTGGACCCTGACACGGCTCACCCGGCCCTGATGCTGTCCCCTGAC CCTCCCAAGTGGACCTGACGCTGGACCCTGACGCGGCTCACCCGGCCCTGATGCTGTCCCCTGAC A G TRIM41 Ensembl:ENSG00000146063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181234187..181234286 26863196 MeRIP-seq:(Medium) rs1429128113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1321120,Human_RBP_ID_15416999,Human_RBP_ID_19015426,Human_RBP_ID_19125163 Human_Splice_Rec_732128,Human_Splice_Rec_732138,Human_Splice_Rec_732146,Human_Splice_Rec_732156,Human_Splice_Rec_732168,Human_Splice_Rec_732180,Human_Splice_Rec_732186 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 91956 RMVar_ID_91956 Human_SNP_ID_264037012 m1A Human chr5 + 181234879 181234879 181234879 TGAGGGCTCAAAGGCTCTTCCCACTGCTTGTTACTGTGTTGCTTCCCACTCCCCCTTGACCCCAG TGAGGGCTCAAAGGCTCTTCCCACTGCTTGTTCCTGTGTTGCTTCCCACTCCCCCTTGACCCCAG A C TRIM41 Ensembl:ENSG00000146063 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181234829..181235033 26863196 MeRIP-seq:(Medium) rs1455767963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1652891,Human_RBP_ID_18046513,Human_RBP_ID_21159094,Human_RBP_ID_21990148,Human_RBP_ID_24101889 Human_miRNA_ID_37921,Human_miRNA_ID_163707,Human_miRNA_ID_308468,Human_miRNA_ID_3083915 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 91957 RMVar_ID_91957 Human_SNP_ID_264037059 m1A Human chr5 + 181234938 181234938 181234938 CCCCAGGCCCCTGCTTCTCCCTCTAGGAGCCTAAAGAACCCTCCTGGCCTCCAGCTCAGCCTTCT CCCCAGGCCCCTGCTTCTCCCTCTAGGAGCCTGAAGAACCCTCCTGGCCTCCAGCTCAGCCTTCT A G TRIM41 Ensembl:ENSG00000146063 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181234888..181235010 26863196 MeRIP-seq:(Medium) rs1199037620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17529585,Human_RBP_ID_25887265,Human_RBP_ID_26791981 Human_Splice_Rec_732158,Human_Splice_Rec_732159,Human_Splice_Rec_732170,Human_Splice_Rec_732171 Human_miRNA_ID_2992579 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 91958 RMVar_ID_91958 Human_SNP_ID_264037069 m1A Human chr5 - 181234950 181234950 181234950 ATAGTAGGTGAGAGAAGGCTGAGCTGGAGGCCAGGAGGGTTCTTTAGGCTCCTAGAGGGAGAAGC ATAGTAGGTGAGAGAAGGCTGAGCTGGAGGCCGGGAGGGTTCTTTAGGCTCCTAGAGGGAGAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181234899..181235024 26863196 MeRIP-seq:(Medium) rs1373219754 Functional Loss SNV dbSNP153 33..33 33 - - - 91959 RMVar_ID_91959 Human_SNP_ID_264037305 m1A Human chr5 - 181235463 181235463 181235463 CCTTGGTTGAGTGCTGGAAAAGGGAAGGGGGAAGAAATAATTTATGTTGATGTAATTAATGTAAT CCTTGGTTGAGTGCTGGAAAAGGGAAGGGGGAGGAAATAATTTATGTTGATGTAATTAATGTAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:181235333..181235510 26863196 MeRIP-seq:(Medium) rs904030674 Functional Loss SNV dbSNP153 33..33 33 - - - 91960 RMVar_ID_91960 Human_SNP_ID_264037342 m1A Human chr5 - 181235559 181235559 181235559 AGGGGCTGGGAGAAAAGCCAGCTCCACTGAACAAAGGGGAGAGGAGCCTGGCAGTGAGCAGACCT AGGGGCTGGGAGAAAAGCCAGCTCCACTGAACGAAGGGGAGAGGAGCCTGGCAGTGAGCAGACCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181235509..181235709 32194978 MeRIP-seq:(Medium) rs991861451 Functional Loss SNV dbSNP153 33..33 33 - - - 91961 RMVar_ID_91961 Human_SNP_ID_264037909 m1A Human chr5 - 181237007 181237007 181237007 CTGTTTGCTGGCTACACGGACAACCTGGTGCGAGTGTGGCAGGTGACCATTGGCACACGCTAGAA CTGTTTGCTGGCTACACGGACAACCTGGTGCGGGTGTGGCAGGTGACCATTGGCACACGCTAGAA T C RACK1 Ensembl:ENSG00000204628 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr5:181236926..181237109;chr5:181236926..181237050 32194978 MeRIP-seq:(Medium) rs548459672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250493,Human_RBP_ID_640631,Human_RBP_ID_788537,Human_RBP_ID_946866,Human_RBP_ID_1041107,Human_RBP_ID_1652913,Human_RBP_ID_1993942,Human_RBP_ID_4828064,Human_RBP_ID_5509462,Human_RBP_ID_7425921,Human_RBP_ID_8612971,Human_RBP_ID_8889171,Human_RBP_ID_9175549,Human_RBP_ID_15417056,Human_RBP_ID_17299990,Human_RBP_ID_17532259,Human_RBP_ID_17662831,Human_RBP_ID_18046536,Human_RBP_ID_18195193,Human_RBP_ID_18840697,Human_RBP_ID_21159136,Human_RBP_ID_22459082,Human_RBP_ID_22512237,Human_RBP_ID_22828291,Human_RBP_ID_23136998,Human_RBP_ID_24101892,Human_RBP_ID_26826959,Human_RBP_ID_27080850,Human_RBP_ID_27160682 Human_Splice_Rec_732200,Human_Splice_Rec_732212,Human_Splice_Rec_732226,Human_Splice_Rec_732230,Human_Splice_Rec_732240,Human_Splice_Rec_732252,Human_Splice_Rec_732260,Human_Splice_Rec_732262,Human_Splice_Rec_732268,Human_Splice_Rec_732292,Human_Splice_Rec_732304,Human_Splice_Rec_732308,Human_Splice_Rec_732320,Human_Splice_Rec_732332,Human_Splice_Rec_732346 RMVar_hsa_circ_76679,RMVar_hsa_circ_108895,RMVar_hsa_circ_117695,RMVar_hsa_circ_124854,RMVar_hsa_circ_112530,RMVar_hsa_circ_88161,RMVar_hsa_circ_97450,RMVar_hsa_circ_83853,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236780,RMVar_hsa_circ_236782,RMVar_hsa_circ_236783,RMVar_hsa_circ_236781,RMVar_hsa_circ_236779,RMVar_hsa_circ_236777 91962 RMVar_ID_91962 Human_SNP_ID_264037921 m1A Human chr5 + 181237040 181237040 181237040 CGCACCAGGTTGTCCGTGTAGCCAGCAAACAGAGTCTGCAGGGAAGAAATGACAGTGACAGGTCA CGCACCAGGTTGTCCGTGTAGCCAGCAAACAGGGTCTGCAGGGAAGAAATGACAGTGACAGGTCA A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:181237004..181237089 26863410 MeRIP-seq:(Medium) rs988088554 Functional Loss SNV dbSNP153 33..33 33 - - - 91963 RMVar_ID_91963 Human_SNP_ID_264037922 m1A Human chr5 + 181237040 181237040 181237040 CGCACCAGGTTGTCCGTGTAGCCAGCAAACAGAGTCTGCAGGGAAGAAATGACAGTGACAGGTCA CGCACCAGGTTGTCCGTGTAGCCAGCAAACAGTGTCTGCAGGGAAGAAATGACAGTGACAGGTCA A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:181237004..181237089 26863410 MeRIP-seq:(Medium) rs988088554 Functional Loss SNV dbSNP153 33..33 33 - - - 91964 RMVar_ID_91964 Human_SNP_ID_264038361 m1A Human chr5 + 181238169 181238166 181238169 AGTAGCGGTTAGGGCTGAAGCACAGGGCGTTGATGATGTCCCCACCATCTAGCGTGTAAAGGTGT AGTAGCGGTTAGGGCTGAAGCACAGGGCGT___TGATGTCCCCACCATCTAGCGTGTAAAGGTGT TTGA T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:181238072..181238287;chr5:181238059..181238310;chr5:181238055..181238295 26863196 MeRIP-seq:(Medium) rs761851164 Functional Loss DEL dbSNP153 31..33 33 - - - 91965 RMVar_ID_91965 Human_SNP_ID_264038404 m1A Human chr5 - 181238285 181238285 181238285 TCTGACAGAATCTTGAGATGGGCAGAATTAACATCTGGAAGAGGTCACAGTGTCCTGATTTACCT TCTGACAGAATCTTGAGATGGGCAGAATTAACCTCTGGAAGAGGTCACAGTGTCCTGATTTACCT T G RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:181237856..181238295 32194978 MeRIP-seq:(Medium) rs1323991737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946870,Human_RBP_ID_1993957,Human_RBP_ID_5397878,Human_RBP_ID_7425945,Human_RBP_ID_15417135,Human_RBP_ID_22512247,Human_RBP_ID_22681153,Human_RBP_ID_23044175,Human_RBP_ID_24101915,Human_RBP_ID_25887314 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_108895,RMVar_hsa_circ_124854,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236780,RMVar_hsa_circ_236779,RMVar_hsa_circ_236777,RMVar_hsa_circ_285736,RMVar_hsa_circ_367719,RMVar_hsa_circ_375994,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236785,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_236786,RMVar_hsa_circ_370058,RMVar_hsa_circ_274824,RMVar_hsa_circ_111645,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_236794,RMVar_hsa_circ_77061,RMVar_hsa_circ_236793,RMVar_hsa_circ_236791 91966 RMVar_ID_91966 Human_SNP_ID_264038700 m1A Human chr5 + 181239046 181239046 181239046 TCCTTCCATGACGCTGTCTTCCACTGAGTAGGAGACGCCTTGTCCCCAAATACCTTGCCTCCAGA TCCTTCCATGACGCTGTCTTCCACTGAGTAGGTGACGCCTTGTCCCCAAATACCTTGCCTCCAGA A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:181239043..181239243 32194978 MeRIP-seq:(Medium) rs746376973 Functional Loss SNV dbSNP153 33..33 33 - - - 91967 RMVar_ID_91967 Human_SNP_ID_264038729 m1A Human chr5 - 181239155 181239155 181239155 GTCTATGCAGGTATGGAACCTGGCTAACTGCAAGCTGAAGACCAACCACATTGGCCACACAGGCT GTCTATGCAGGTATGGAACCTGGCTAACTGCAGGCTGAAGACCAACCACATTGGCCACACAGGCT T C RACK1 Ensembl:ENSG00000204628 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181239036..181239200 26863196 MeRIP-seq:(Medium) rs772588134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640660,Human_RBP_ID_946872,Human_RBP_ID_1652953,Human_RBP_ID_1993961,Human_RBP_ID_2922511,Human_RBP_ID_3767506,Human_RBP_ID_4854271,Human_RBP_ID_8612985,Human_RBP_ID_9175558,Human_RBP_ID_15417193,Human_RBP_ID_17300001,Human_RBP_ID_17413355,Human_RBP_ID_17532262,Human_RBP_ID_18195203,Human_RBP_ID_18357556,Human_RBP_ID_18840731,Human_RBP_ID_22460372,Human_RBP_ID_22534004,Human_RBP_ID_24101923,Human_RBP_ID_27080875 Human_Splice_Rec_732194,Human_Splice_Rec_732195,Human_Splice_Rec_732206,Human_Splice_Rec_732207,Human_Splice_Rec_732220,Human_Splice_Rec_732221,Human_Splice_Rec_732244,Human_Splice_Rec_732245,Human_Splice_Rec_732258,Human_Splice_Rec_732259,Human_Splice_Rec_732264,Human_Splice_Rec_732265,Human_Splice_Rec_732272,Human_Splice_Rec_732273,Human_Splice_Rec_732286,Human_Splice_Rec_732287,Human_Splice_Rec_732298,Human_Splice_Rec_732299,Human_Splice_Rec_732314,Human_Splice_Rec_732315,Human_Splice_Rec_732326,Human_Splice_Rec_732327,Human_Splice_Rec_732340,Human_Splice_Rec_732341,Human_Splice_Rec_732352,Human_Splice_Rec_732353,Human_Splice_Rec_732360,Human_Splice_Rec_732361,Human_Splice_Rec_732368,Human_Splice_Rec_732369,Human_Splice_Rec_732376,Human_Splice_Rec_732386,Human_Splice_Rec_732394,Human_Splice_Rec_732402,Human_Splice_Rec_732410 Human_miRNA_ID_1348610,Human_miRNA_ID_1812154 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_108895,RMVar_hsa_circ_124854,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236780,RMVar_hsa_circ_236779,RMVar_hsa_circ_236777,RMVar_hsa_circ_285736,RMVar_hsa_circ_367719,RMVar_hsa_circ_375994,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236785,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_236786,RMVar_hsa_circ_370058,RMVar_hsa_circ_274824,RMVar_hsa_circ_111645,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_236794,RMVar_hsa_circ_77061,RMVar_hsa_circ_236793,RMVar_hsa_circ_236791,RMVar_hsa_circ_236799,RMVar_hsa_circ_321619,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_343960,RMVar_hsa_circ_374992,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_236797,RMVar_hsa_circ_236798,RMVar_hsa_circ_357112 91968 RMVar_ID_91968 Human_SNP_ID_264038850 m1A Human chr5 - 181239438 181239438 181239438 GGCAGGGGCTTTACCAGTCAGGGTGTGCTCCCAGGTGGTCATACACTCCAAGTCCTGTGGAAAGC GGCAGGGGCTTTACCAGTCAGGGTGTGCTCCCGGGTGGTCATACACTCCAAGTCCTGTGGAAAGC T C RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181239436..181239629 26863196 MeRIP-seq:(Medium) rs1205911091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5397880,Human_RBP_ID_15417222,Human_RBP_ID_19125164 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_108895,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236779,RMVar_hsa_circ_236777,RMVar_hsa_circ_285736,RMVar_hsa_circ_367719,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_236786,RMVar_hsa_circ_370058,RMVar_hsa_circ_274824,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_77061,RMVar_hsa_circ_236793,RMVar_hsa_circ_236791,RMVar_hsa_circ_236799,RMVar_hsa_circ_321619,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_374992,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_236798 91969 RMVar_ID_91969 Human_SNP_ID_264039567 m1A Human chr5 + 181241438 181241438 181241438 GGCAAGAGTGAGACTGTCGCCAAAAAAAAAAAAAAAAAGCAAAGTTTAAGAGGGTGGAAGAGATC GGCAAGAGTGAGACTGTCGCCAAAAAAAAAAACAAAAAGCAAAGTTTAAGAGGGTGGAAGAGATC A C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:181241436..181241521 26863410 MeRIP-seq:(Medium) rs945783157 Functional Loss SNV dbSNP153 33..33 33 - - - 91970 RMVar_ID_91970 Human_SNP_ID_264039568 m1A Human chr5 + 181241438 181241438 181241438 GGCAAGAGTGAGACTGTCGCCAAAAAAAAAAAAAAAAAGCAAAGTTTAAGAGGGTGGAAGAGATC GGCAAGAGTGAGACTGTCGCCAAAAAAAAAAAGAAAAAGCAAAGTTTAAGAGGGTGGAAGAGATC A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:181241436..181241521 26863410 MeRIP-seq:(Medium) rs945783157 Functional Loss SNV dbSNP153 33..33 33 - - - 91971 RMVar_ID_91971 Human_SNP_ID_264039582 m1A Human chr5 - 181241452 181241448 181241452 GAGCCATCTCCAAGGATCTCTTCCACCCTCTTAAACTTTGCTTTTTTTTTTTTTTTTTGGCGACA GAGCCATCTCCAAGGATCTCTTCCACCCTCTT____TTTGCTTTTTTTTTTTTTTTTTGGCGACA AGTTT A RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181241450..181241684 26863196 MeRIP-seq:(Medium) rs776768489 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_19127030,Human_RBP_ID_23044204 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236777,RMVar_hsa_circ_367719,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_274824,RMVar_hsa_circ_44697,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_77061,RMVar_hsa_circ_236791,RMVar_hsa_circ_236799,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_374992,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_279559,RMVar_hsa_circ_302064,RMVar_hsa_circ_236803,RMVar_hsa_circ_79962,RMVar_hsa_circ_87613,RMVar_hsa_circ_236805,RMVar_hsa_circ_236806 91972 RMVar_ID_91972 Human_SNP_ID_264039586 m1A Human chr5 - 181241452 181241452 181241452 GAGCCATCTCCAAGGATCTCTTCCACCCTCTTAAACTTTGCTTTTTTTTTTTTTTTTTGGCGACA GAGCCATCTCCAAGGATCTCTTCCACCCTCTTTAACTTTGCTTTTTTTTTTTTTTTTTGGCGACA T A RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181241450..181241684 26863196 MeRIP-seq:(Medium) rs779197489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19127030,Human_RBP_ID_23044204 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236777,RMVar_hsa_circ_367719,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_274824,RMVar_hsa_circ_44697,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_77061,RMVar_hsa_circ_236791,RMVar_hsa_circ_236799,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_374992,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_279559,RMVar_hsa_circ_302064,RMVar_hsa_circ_236803,RMVar_hsa_circ_79962,RMVar_hsa_circ_87613,RMVar_hsa_circ_236805,RMVar_hsa_circ_236806 91973 RMVar_ID_91973 Human_SNP_ID_264039587 m1A Human chr5 - 181241452 181241452 181241452 GAGCCATCTCCAAGGATCTCTTCCACCCTCTTAAACTTTGCTTTTTTTTTTTTTTTTTGGCGACA GAGCCATCTCCAAGGATCTCTTCCACCCTCTTCAACTTTGCTTTTTTTTTTTTTTTTTGGCGACA T G RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181241450..181241684 26863196 MeRIP-seq:(Medium) rs779197489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19127030,Human_RBP_ID_23044204 RMVar_hsa_circ_92324,RMVar_hsa_circ_76679,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236777,RMVar_hsa_circ_367719,RMVar_hsa_circ_286696,RMVar_hsa_circ_90860,RMVar_hsa_circ_236787,RMVar_hsa_circ_236788,RMVar_hsa_circ_274824,RMVar_hsa_circ_44697,RMVar_hsa_circ_236790,RMVar_hsa_circ_236792,RMVar_hsa_circ_77061,RMVar_hsa_circ_236791,RMVar_hsa_circ_236799,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_374992,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_279559,RMVar_hsa_circ_302064,RMVar_hsa_circ_236803,RMVar_hsa_circ_79962,RMVar_hsa_circ_87613,RMVar_hsa_circ_236805,RMVar_hsa_circ_236806 91974 RMVar_ID_91974 Human_SNP_ID_264039602 m1A Human chr5 + 181241476 181241476 181241476 GCAAAGTTTAAGAGGGTGGAAGAGATCCTTGGAGATGGCTCACTTTACCTGGACAGTGTATTTGC GCAAAGTTTAAGAGGGTGGAAGAGATCCTTGGTGATGGCTCACTTTACCTGGACAGTGTATTTGC A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:181241472..181241650 32194978 MeRIP-seq:(Medium) rs1389434490 Functional Loss SNV dbSNP153 33..33 33 - - - 91975 RMVar_ID_91975 Human_SNP_ID_264039830 m1A Human chr5 + 181242131 181242131 181242131 ACCAGCCAATTGCATCCACCTCACTTCTGCCCAGATTCTTCCCAAGGCCCCAGAGCTAAGTGAGC ACCAGCCAATTGCATCCACCTCACTTCTGCCCGGATTCTTCCCAAGGCCCCAGAGCTAAGTGAGC A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181242126..181242150 26863196 MeRIP-seq:(Medium) rs1200474021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236812 91976 RMVar_ID_91976 Human_SNP_ID_264039881 m1A Human chr5 - 181242345 181242345 181242345 CACTGATTTTTCTTCTGTTTTACCTCCTTTAGATAAGACCATCATCATGTGGAAACTGACCAGGG CACTGATTTTTCTTCTGTTTTACCTCCTTTAGGTAAGACCATCATCATGTGGAAACTGACCAGGG T C RACK1 Ensembl:ENSG00000204628 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181242127..181242393 26863196 MeRIP-seq:(Medium) rs1464679422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77201,Human_RBP_ID_640675,Human_RBP_ID_788550,Human_RBP_ID_1652984,Human_RBP_ID_1993979,Human_RBP_ID_5276533,Human_RBP_ID_8613009,Human_RBP_ID_15417369,Human_RBP_ID_18195213,Human_RBP_ID_26827803,Human_RBP_ID_27739474 Human_Splice_Rec_732190,Human_Splice_Rec_732202,Human_Splice_Rec_732214,Human_Splice_Rec_732254,Human_Splice_Rec_732280,Human_Splice_Rec_732310,Human_Splice_Rec_732322,Human_Splice_Rec_732334,Human_Splice_Rec_732348,Human_Splice_Rec_732356,Human_Splice_Rec_732364,Human_Splice_Rec_732372,Human_Splice_Rec_732378,Human_Splice_Rec_732388,Human_Splice_Rec_732396,Human_Splice_Rec_732397,Human_Splice_Rec_732404,Human_Splice_Rec_732414,Human_Splice_Rec_732424,Human_Splice_Rec_732428,Human_Splice_Rec_732432,Human_Splice_Rec_732436,Human_Splice_Rec_732440 RMVar_hsa_circ_92324,RMVar_hsa_circ_112530,RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_236777,RMVar_hsa_circ_367719,RMVar_hsa_circ_90860,RMVar_hsa_circ_236788,RMVar_hsa_circ_44697,RMVar_hsa_circ_236790,RMVar_hsa_circ_77061,RMVar_hsa_circ_236791,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_83006,RMVar_hsa_circ_307175,RMVar_hsa_circ_236800,RMVar_hsa_circ_236801,RMVar_hsa_circ_302064,RMVar_hsa_circ_79325,RMVar_hsa_circ_79962,RMVar_hsa_circ_87613,RMVar_hsa_circ_236805,RMVar_hsa_circ_236806,RMVar_hsa_circ_284706,RMVar_hsa_circ_82079,RMVar_hsa_circ_236810,RMVar_hsa_circ_236811,RMVar_hsa_circ_236809,RMVar_hsa_circ_95427,RMVar_hsa_circ_236813 91977 RMVar_ID_91977 Human_SNP_ID_264040444 m1A Human chr5 + 181243748 181243748 181243748 CCGGGAACTGCGGGGTAGTAGCGATCTGGGTTACCCAGCCGTTGTGGCCCTTGAGGGTGCCACGA CCGGGAACTGCGGGGTAGTAGCGATCTGGGTTCCCCAGCCGTTGTGGCCCTTGAGGGTGCCACGA A C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181243698..181243833 26863196 MeRIP-seq:(Medium) rs745953408 Functional Loss SNV dbSNP153 33..33 33 - - - 91978 RMVar_ID_91978 Human_SNP_ID_264040445 m1A Human chr5 + 181243748 181243748 181243748 CCGGGAACTGCGGGGTAGTAGCGATCTGGGTTACCCAGCCGTTGTGGCCCTTGAGGGTGCCACGA CCGGGAACTGCGGGGTAGTAGCGATCTGGGTTGCCCAGCCGTTGTGGCCCTTGAGGGTGCCACGA A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181243698..181243833 26863196 MeRIP-seq:(Medium) rs745953408 Functional Loss SNV dbSNP153 33..33 33 - - - 91979 RMVar_ID_91979 Human_SNP_ID_264040491 m1A Human chr5 + 181243843 181243843 181243843 AGAGCGTGTGTCGCTGCAGCGACGAGGATGGCACTGGATGGCTTAGAGAAACTAGCACCACAACC AGAGCGTGTGTCGCTGCAGCGACGAGGATGGCTCTGGATGGCTTAGAGAAACTAGCACCACAACC A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:181243676..181243925;chr5:181243636..181243925 26863196 MeRIP-seq:(Medium) rs1215916081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236816 91980 RMVar_ID_91980 Human_SNP_ID_264041265 m1A Human chr5 - 181246584 181246576 181246585 GCTGCCAGAATCGCCTATTTTTAGTGAAAGAGAACCGGGCCGGGAGACGGCGGCAGGGGGCCGGA GCTGCCAGAATCGCCTATTTTTAGTGAAAGA_________CGGGAGACGGCGGCAGGGGGCCGGA GGCCCGGTTC G RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181246533..181246658 26863196 MeRIP-seq:(Medium) rs1413099278 Functional Loss DEL dbSNP153 32..40 33 - - - 91981 RMVar_ID_91981 Human_SNP_ID_264041293 m1A Human chr5 - 181246721 181246705 181246721 CGAATCCTGCAGGGTCTGGTCGTCGGAAAGCCAACCATACAGTCAGCCCTCCCTCTCCTCGGGCT CGAATCCTGCAGGGTCTGGTCGTCGGAAAGCC________________CTCCCTCTCCTCGGGCT GGGCTGACTGTATGGTT G RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:181246670..181246869 32194978 MeRIP-seq:(Medium) rs1433440407 Functional Loss DEL dbSNP153 33..48 33 - - - 91982 RMVar_ID_91982 Human_SNP_ID_264044864 m1A Human chr5 + 181260573 181260573 181260573 AGCATTCCCCCGATACAACACCTCTCGAATGGAGCCGTCCCATCCATCCATGGCCCCCACCGCTT AGCATTCCCCCGATACAACACCTCTCGAATGGGGCCGTCCCATCCATCCATGGCCCCCACCGCTT A G AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181260345..181260753 26863196 MeRIP-seq:(Medium) rs1030622696 Functional Loss SNV dbSNP153 33..33 33 - - - 91983 RMVar_ID_91983 Human_SNP_ID_264045054 m1A Human chr5 - 181261090 181261090 181261090 AGCGGCTGCATCTGAGGCGGACGCCGCAGTGTAGGGCACACCCTGAGGGTAGCGAGAGACGTGAC AGCGGCTGCATCTGAGGCGGACGCCGCAGTGTGGGGCACACCCTGAGGGTAGCGAGAGACGTGAC T C TRIM52 Ensembl:ENSG00000183718 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181260938..181261139 26863196 MeRIP-seq:(Medium) rs959435441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18425070 91984 RMVar_ID_91984 Human_SNP_ID_264050627 m1A Human chr5 + 181281648 181281648 181281648 GGCGGGAGCTGGAGCAGTAAGAGGGCGGCCTGAGCGGTAGGAGGGGGGCTGGAGCAGTAAGAGGG GGCGGGAGCTGGAGCAGTAAGAGGGCGGCCTGGGCGGTAGGAGGGGGGCTGGAGCAGTAAGAGGG A G AC008443.3 Ensembl:ENSG00000248103 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:181281636..181281719 26863196 MeRIP-seq:(Medium) rs56197940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5242351,Human_RBP_ID_9437019,Human_RBP_ID_24385702 91985 RMVar_ID_91985 Human_SNP_ID_525475462 m1A Human chr13 - 30272909 30272909 30272909 TAGAGGTGAGCGCTTATGCAATCATTTCAGCAAGGAGAAAAATGTAAGCAAGACTATCTGAGATT TAGAGGTGAGCGCTTATGCAATCATTTCAGCAGGGAGAAAAATGTAAGCAAGACTATCTGAGATT T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:30272905..30273088 26863196 MeRIP-seq:(Medium) rs1199211500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162518,RMVar_hsa_circ_162519,RMVar_hsa_circ_162522,RMVar_hsa_circ_10720,RMVar_hsa_circ_273955,RMVar_hsa_circ_162526,RMVar_hsa_circ_162527,RMVar_hsa_circ_162531,RMVar_hsa_circ_315407,RMVar_hsa_circ_366410,RMVar_hsa_circ_162532,RMVar_hsa_circ_162535,RMVar_hsa_circ_288207,RMVar_hsa_circ_321933,RMVar_hsa_circ_162537 91986 RMVar_ID_91986 Human_SNP_ID_525475464 m1A Human chr13 - 30272918 30272918 30272918 GGGCAGATATAGAGGTGAGCGCTTATGCAATCATTTCAGCAAGGAGAAAAATGTAAGCAAGACTA GGGCAGATATAGAGGTGAGCGCTTATGCAATCTTTTCAGCAAGGAGAAAAATGTAAGCAAGACTA T A KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:30272911..30273015 26863196 MeRIP-seq:(Medium) rs1248742444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162518,RMVar_hsa_circ_162519,RMVar_hsa_circ_162522,RMVar_hsa_circ_10720,RMVar_hsa_circ_273955,RMVar_hsa_circ_162526,RMVar_hsa_circ_162527,RMVar_hsa_circ_162531,RMVar_hsa_circ_315407,RMVar_hsa_circ_366410,RMVar_hsa_circ_162532,RMVar_hsa_circ_162535,RMVar_hsa_circ_288207,RMVar_hsa_circ_321933,RMVar_hsa_circ_162537 91987 RMVar_ID_91987 Human_SNP_ID_525483944 m1A Human chr13 - 30306951 30306951 30306951 TGGTCGCGGACCTGGGCTCTGTGCGTTGGGAAAGGGAAGTGGAGGTGAGCCTCGGGCTTCCCGCC TGGTCGCGGACCTGGGCTCTGTGCGTTGGGAAGGGGAAGTGGAGGTGAGCCTCGGGCTTCCCGCC T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:30306823..30306950 26863196 MeRIP-seq:(Medium) rs955709186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453429 91988 RMVar_ID_91988 Human_SNP_ID_525484077 m1A Human chr13 - 30307275 30307275 30307275 CGAGGGCGAGACAGCAGGTGGTGGAGGGCTCTAGCCAACAGCCCCTCTCGGCCTCCCACTGCCGG CGAGGGCGAGACAGCAGGTGGTGGAGGGCTCTGGCCAACAGCCCCTCTCGGCCTCCCACTGCCGG T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:30307265..30307536 26863196 MeRIP-seq:(Medium) rs543980916 Functional Loss SNV dbSNP153 33..33 33 - - - 91989 RMVar_ID_91989 Human_SNP_ID_525484109 m1A Human chr13 + 30307393 30307393 30307393 GATGCGGTCCAGATGGGGTGCGGGTGGGGCGCAGGCCGCCGCCGCCGCCGCCGCCGAGTCCGTTA GATGCGGTCCAGATGGGGTGCGGGTGGGGCGCCGGCCGCCGCCGCCGCCGCCGCCGAGTCCGTTA A C lnc-UBE2L5-2,lnc-UBE2L5-2:2,lnc-UBE2L5-2:3,lnc-UBE2L5-2:4 RNACentral:URS0000D583EA,RNACentral:URS0000D5C7F1,RNACentral:URS0000D5734A,RNACentral:URS0000D5B352 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:30307269..30307408 26863196 MeRIP-seq:(Medium) rs1247007244 Functional Loss SNV dbSNP153 33..33 33 - - - 91990 RMVar_ID_91990 Human_SNP_ID_525522708 m1A Human chr13 - 30463694 30463694 30463694 TGCTAACATCAAATATTTATTTTATTTTTTAGAAAAATAACTAAACATGGGCAAAGGAGATCCTA TGCTAACATCAAATATTTATTTTATTTTTTAGGAAAATAACTAAACATGGGCAAAGGAGATCCTA T C HMGB1 Ensembl:ENSG00000189403 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:30463601..30463754 26863410 MeRIP-seq:(Medium) rs200537410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230744,Human_RBP_ID_4276578,Human_RBP_ID_5140522,Human_RBP_ID_6319212,Human_RBP_ID_9367410,Human_RBP_ID_17244533,Human_RBP_ID_22737266,Human_RBP_ID_25041548,Human_RBP_ID_26324026 Human_Splice_Rec_1453552,Human_Splice_Rec_1453560,Human_Splice_Rec_1453568,Human_Splice_Rec_1453590,Human_Splice_Rec_1453600 91991 RMVar_ID_91991 Human_SNP_ID_525522970 m1A Human chr13 - 30464401 30464401 30464401 AAAAAATACTTCCCGAGTTGGGGGAGGGGGCCACCGAGCCACGAGCAGGAGTGGCTTTTGTCCCT AAAAAATACTTCCCGAGTTGGGGGAGGGGGCCGCCGAGCCACGAGCAGGAGTGGCTTTTGTCCCT T C HMGB1 Ensembl:ENSG00000189403 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:30464350..30464553 32194978 MeRIP-seq:(Medium) rs1043489095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756277 91992 RMVar_ID_91992 Human_SNP_ID_525523148 m1A Human chr13 + 30464738 30464738 30464738 CCTGCGCCGCCGCCGCCGCGAGGGCGAGCGCGAGCGAGAATATGGCTCCTTCCCTTTGTGTGTGT CCTGCGCCGCCGCCGCCGCGAGGGCGAGCGCGGGCGAGAATATGGCTCCTTCCCTTTGTGTGTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:30464505..30464855 26863196 MeRIP-seq:(Medium) rs1465170402 Functional Loss SNV dbSNP153 33..33 33 - - - 91993 RMVar_ID_91993 Human_SNP_ID_525523150 m1A Human chr13 + 30464742 30464742 30464742 CGCCGCCGCCGCCGCGAGGGCGAGCGCGAGCGAGAATATGGCTCCTTCCCTTTGTGTGTGTGTGT CGCCGCCGCCGCCGCGAGGGCGAGCGCGAGCGCGAATATGGCTCCTTCCCTTTGTGTGTGTGTGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:30464330..30464814 26863196 MeRIP-seq:(Medium) rs1190123381 Functional Loss SNV dbSNP153 33..33 33 - - - 91994 RMVar_ID_91994 Human_SNP_ID_525523151 m1A Human chr13 + 30464742 30464742 30464742 CGCCGCCGCCGCCGCGAGGGCGAGCGCGAGCGAGAATATGGCTCCTTCCCTTTGTGTGTGTGTGT CGCCGCCGCCGCCGCGAGGGCGAGCGCGAGCGTGAATATGGCTCCTTCCCTTTGTGTGTGTGTGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:30464330..30464814 26863196 MeRIP-seq:(Medium) rs1190123381 Functional Loss SNV dbSNP153 33..33 33 - - - 91995 RMVar_ID_91995 Human_SNP_ID_525523821 m1A Human chr13 - 30465852 30465852 30465852 AGCCATTGCAGTACATTGAGCTCCATAGAGACAGCACCGGGGCAAGTGAGAGCCGGACGGGCACT AGCCATTGCAGTACATTGAGCTCCATAGAGACTGCACCGGGGCAAGTGAGAGCCGGACGGGCACT T A HMGB1 Ensembl:ENSG00000189403 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:30465801..30465918 26863410 MeRIP-seq:(Medium) rs1565996406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9367412,Human_RBP_ID_26914987 Human_Splice_Rec_1453551,Human_Splice_Rec_1453589,Human_Splice_Rec_1453599 91996 RMVar_ID_91996 Human_SNP_ID_525523852 m1A Human chr13 - 30465913 30465913 30465913 CTGGAGAGTAATGTTACAGAGCGGAGAGAGTGAGGAGGCTGCGTCTGGCTCCCGCTCTCACAGCC CTGGAGAGTAATGTTACAGAGCGGAGAGAGTGGGGAGGCTGCGTCTGGCTCCCGCTCTCACAGCC T C HMGB1 Ensembl:ENSG00000189403 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1293769481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230748,Human_RBP_ID_756281,Human_RBP_ID_4276579,Human_RBP_ID_5645606,Human_RBP_ID_6270521,Human_RBP_ID_8792047,Human_RBP_ID_9323451,Human_RBP_ID_9367412,Human_RBP_ID_18417866,Human_RBP_ID_22438393,Human_RBP_ID_26324308 91997 RMVar_ID_91997 Human_SNP_ID_525542019 m1A Human chr13 - 30538752 30538751 30538753 AAAGAAGGAAAGAGAGAGAGAAAGAGAAAGAAAGAAAAAGAAGAAAGAAAGAAAAAGAAAGAAAA AAAGAAGGAAAGAGAGAGAGAAAGAGAAAGA__GAAAAAGAAGAAAGAAAGAAAAAGAAAGAAAA CTT C HMGB1 Ensembl:ENSG00000189403 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:30538419..30538836 26863196 MeRIP-seq:(Medium) rs1349979975 Functional Loss DEL dbSNP153 32..33 33 - - - 91998 RMVar_ID_91998 Human_SNP_ID_525560951 m1A Human chr13 + 30617935 30617935 30617935 GACTCAAGCCGGAAGCCGCCTTCCTAGTGGAGACGCGAGTGGGGGAGGAGCAGTCCGAGGGGAAC GACTCAAGCCGGAAGCCGCCTTCCTAGTGGAGGCGCGAGTGGGGGAGGAGCAGTCCGAGGGGAAC A G USPL1 Ensembl:ENSG00000132952 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:30617886..30618245 26863196 MeRIP-seq:(Medium) rs898128061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434781,Human_RBP_ID_18417773 91999 RMVar_ID_91999 Human_SNP_ID_525560971 m1A Human chr13 - 30617992 30617985 30617993 TCGATCGGAACTCCTGTTCCAGCTTGATCTCCACCCTAGTTGCAACGTTCAACCCACGTTCCCCT TCGATCGGAACTCCTGTTCCAGCTTGATCTC________TTGCAACGTTCAACCCACGTTCCCCT ACTAGGGTG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:30617941..30621107 26863196 MeRIP-seq:(Medium) rs1009357256 Functional Loss DEL dbSNP153 32..39 33 - - - 92000 RMVar_ID_92000 Human_SNP_ID_525695484 m1A Human chr13 + 31138452 31138452 31138452 TTAATTTCCTGAGCACGTACAACTGGATCCTGATCAAGACTCTTTTTAGCCTGAGCATTCATGAC TTAATTTCCTGAGCACGTACAACTGGATCCTGGTCAAGACTCTTTTTAGCCTGAGCATTCATGAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:31137520..31138552 32194978 MeRIP-seq:(Medium) rs776636320 Functional Loss SNV dbSNP153 33..33 33 - - - 92001 RMVar_ID_92001 Human_SNP_ID_525695485 m1A Human chr13 + 31138452 31138452 31138452 TTAATTTCCTGAGCACGTACAACTGGATCCTGATCAAGACTCTTTTTAGCCTGAGCATTCATGAC TTAATTTCCTGAGCACGTACAACTGGATCCTGTTCAAGACTCTTTTTAGCCTGAGCATTCATGAC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:31137520..31138552 32194978 MeRIP-seq:(Medium) rs776636320 Functional Loss SNV dbSNP153 33..33 33 - - - 92002 RMVar_ID_92002 Human_SNP_ID_525701432 m1A Human chr13 - 31158856 31158856 31158856 TTTTTTGGAATATATTTTTTTCTAGGTCAGTCATATCATTTGGATCAAAAAATAGAACAATCGGA TTTTTTGGAATATATTTTTTTCTAGGTCAGTCGTATCATTTGGATCAAAAAATAGAACAATCGGA T C HSPH1 Ensembl:ENSG00000120694 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:31158801..31158875 26863196 MeRIP-seq:(Medium) rs1284464370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453802,Human_Splice_Rec_1453803,Human_Splice_Rec_1453836,Human_Splice_Rec_1453837,Human_Splice_Rec_1453870,Human_Splice_Rec_1453871,Human_Splice_Rec_1453904,Human_Splice_Rec_1453905,Human_Splice_Rec_1453936,Human_Splice_Rec_1453937,Human_Splice_Rec_1453990,Human_Splice_Rec_1453991 RMVar_hsa_circ_52313,RMVar_hsa_circ_61590,RMVar_hsa_circ_84872,RMVar_hsa_circ_24204,RMVar_hsa_circ_162564,RMVar_hsa_circ_69474,RMVar_hsa_circ_162565,RMVar_hsa_circ_107302 92003 RMVar_ID_92003 Human_SNP_ID_525702477 m1A Human chr13 - 31161680 31161680 31161680 CAGAGGAACGGCCAGACCCCGCGGGCCGGAGCAGAACGCGGCCAGGGCAGAAAGCGGCGGCAGGA CAGAGGAACGGCCAGACCCCGCGGGCCGGAGCGGAACGCGGCCAGGGCAGAAAGCGGCGGCAGGA T C HSPH1 Ensembl:ENSG00000120694 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:31161631..31161758 32194978 MeRIP-seq:(Medium) rs1437609785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434840,Human_RBP_ID_4267979,Human_RBP_ID_9281282,Human_RBP_ID_22438394,Human_RBP_ID_26756102 Human_miRNA_ID_3090743 RMVar_hsa_circ_84872,RMVar_hsa_circ_162564 92004 RMVar_ID_92004 Human_SNP_ID_525702551 m1A Human chr13 + 31161804 31161804 31161804 ACAGCGGCGGCTGGCTGATAAGAAACCCTGGGAGAAAGCGGGGCTCAGCCTCCGCAGGTCGCTCC ACAGCGGCGGCTGGCTGATAAGAAACCCTGGGTGAAAGCGGGGCTCAGCCTCCGCAGGTCGCTCC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:31161727..31161880 26863196 MeRIP-seq:(Medium) rs1202508340 Functional Loss SNV dbSNP153 33..33 33 - - - 92005 RMVar_ID_92005 Human_SNP_ID_525702572 m1A Human chr13 + 31161839 31161839 31161839 AAGCGGGGCTCAGCCTCCGCAGGTCGCTCCGCACCTCGGGTTGCCTGCCTCACTCTGCCGCGGCT AAGCGGGGCTCAGCCTCCGCAGGTCGCTCCGCGCCTCGGGTTGCCTGCCTCACTCTGCCGCGGCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:31161551..31161900 26863410 MeRIP-seq:(Medium) rs1395711122 Functional Loss SNV dbSNP153 33..33 33 - - - 92006 RMVar_ID_92006 Human_SNP_ID_525702577 m1A Human chr13 - 31161852 31161852 31161852 GCGCCGGTGTGCGAGCCGCGGCAGAGTGAGGCAGGCAACCCGAGGTGCGGAGCGACCTGCGGAGG GCGCCGGTGTGCGAGCCGCGGCAGAGTGAGGCGGGCAACCCGAGGTGCGGAGCGACCTGCGGAGG T C HSPH1 Ensembl:ENSG00000120694 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:31161412..31162000 26863196 MeRIP-seq:(Medium) rs983069135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755964,Human_RBP_ID_812110,Human_RBP_ID_879964,Human_RBP_ID_4267989,Human_RBP_ID_8725588,Human_RBP_ID_8791980,Human_RBP_ID_18417706,Human_RBP_ID_26915110,Human_RBP_ID_27837107 RMVar_hsa_circ_84872,RMVar_hsa_circ_162564 92007 RMVar_ID_92007 Human_SNP_ID_525702590 m1A Human chr13 + 31161877 31161877 31161877 GGTTGCCTGCCTCACTCTGCCGCGGCTCGCACACCGGCGCCGGCGCTGAACTACCGACCCAAAAG GGTTGCCTGCCTCACTCTGCCGCGGCTCGCACCCCGGCGCCGGCGCTGAACTACCGACCCAAAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:31158822..31162038;chr13:31155621..31162038 26863196 MeRIP-seq:(Medium) rs1163563734 Functional Loss SNV dbSNP153 33..33 33 - - - 92008 RMVar_ID_92008 Human_SNP_ID_525702596 m1A Human chr13 - 31161891 31161885 31161891 AAGTGGGACCTCCCCTTTTGGGTCGGTAGTTCAGCGCCGGCGCCGGTGTGCGAGCCGCGGCAGAG AAGTGGGACCTCCCCTTTTGGGTCGGTAGTTC______GGCGCCGGTGTGCGAGCCGCGGCAGAG CGGCGCT C HSPH1 Ensembl:ENSG00000120694 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:31161501..31162038 26863196 MeRIP-seq:(Medium) rs1482473196 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_755964,Human_RBP_ID_812110,Human_RBP_ID_4267992,Human_RBP_ID_8725588,Human_RBP_ID_8791980,Human_RBP_ID_18417706,Human_RBP_ID_27837107 RMVar_hsa_circ_84872,RMVar_hsa_circ_162564 92009 RMVar_ID_92009 Human_SNP_ID_525702613 m1A Human chr13 + 31161905 31161905 31161905 GCACACCGGCGCCGGCGCTGAACTACCGACCCAAAAGGGGAGGTCCCACTTCCTCAGCCTTATGT GCACACCGGCGCCGGCGCTGAACTACCGACCCGAAAGGGGAGGTCCCACTTCCTCAGCCTTATGT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:31161814..31161929 26863196 MeRIP-seq:(Medium) rs1456075559 Functional Loss SNV dbSNP153 33..33 33 - - - 92010 RMVar_ID_92010 Human_SNP_ID_525713157 m1A Human chr13 + 31200012 31200012 31200012 AGGGTCAGCCGCGGCGGCAGGGCGGCGGCGGCAGCGGCGCAGCTCCGCTCCCCGCGCGTCTCCCT AGGGTCAGCCGCGGCGGCAGGGCGGCGGCGGCCGCGGCGCAGCTCCGCTCCCCGCGCGTCTCCCT A C B3GLCT Ensembl:ENSG00000187676 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:31199967..31200140 26863196 MeRIP-seq:(Medium) rs1157422682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_434841,Human_RBP_ID_4276768,Human_RBP_ID_18417774 92011 RMVar_ID_92011 Human_SNP_ID_525717103 m1A Human chr13 + 31215005 31215005 31215005 AGCAAAACTGTTGGATGTGAGAATTAACCTGAATTGCTAATTCTAAGGTAGAAATATTTCTTTTT AGCAAAACTGTTGGATGTGAGAATTAACCTGAGTTGCTAATTCTAAGGTAGAAATATTTCTTTTT A G B3GLCT Ensembl:ENSG00000187676 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:31214974..31215063 26863410 MeRIP-seq:(Medium) rs1197662380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453997 92012 RMVar_ID_92012 Human_SNP_ID_525722014 m1A Human chr13 + 31235137 31235137 31235137 GCTGCAGGGCCAGAATGGTGGGAGATGGACCCAGGCTGGAGAGAATGGCAGGGACGCTTCCAGCT GCTGCAGGGCCAGAATGGTGGGAGATGGACCCGGGCTGGAGAGAATGGCAGGGACGCTTCCAGCT A G B3GLCT Ensembl:ENSG00000187676 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:31235100..31235265 26863196 MeRIP-seq:(Medium) rs1421892228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1680,RMVar_hsa_circ_162567,RMVar_hsa_circ_334977,RMVar_hsa_circ_347429,RMVar_hsa_circ_271177,RMVar_hsa_circ_38576,RMVar_hsa_circ_68627,RMVar_hsa_circ_2329,RMVar_hsa_circ_162568,RMVar_hsa_circ_312139,RMVar_hsa_circ_322542,RMVar_hsa_circ_303788,RMVar_hsa_circ_162569 92013 RMVar_ID_92013 Human_SNP_ID_525734589 m1A Human chr13 + 31287180 31287180 31287180 GATGGAGCTGAGAGTCTCAGGAGACCAAGGCTATTACAGTTTGCAGGACAGAGTACCAGAGAGGA GATGGAGCTGAGAGTCTCAGGAGACCAAGGCTGTTACAGTTTGCAGGACAGAGTACCAGAGAGGA A G B3GLCT Ensembl:ENSG00000187676 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:31287166..31287231 26863196 MeRIP-seq:(Medium) rs947578413 Functional Loss SNV dbSNP153 33..33 33 - - - 92014 RMVar_ID_92014 Human_SNP_ID_526014577 m1A Human chr13 + 32399995 32399995 32399995 TTTAGTAGAGACTGGGTTTTACCATGTTGGCCAAGCTGGTCTCAAACTCCTGATGTCAGGTGATC TTTAGTAGAGACTGGGTTTTACCATGTTGGCCGAGCTGGTCTCAAACTCCTGATGTCAGGTGATC A G BRCA2 Ensembl:ENSG00000139618 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1426227797 Functional Loss SNV dbSNP153 33..33 33 - - - 92015 RMVar_ID_92015 Human_SNP_ID_526048175 m1A Human chr13 + 32538748 32538748 32538748 CTAAAGCCGAGGTCTGGAGGGACTAAAAGCCCACCTCTCAGAATCGCGGTAACAAACCTCACCTC CTAAAGCCGAGGTCTGGAGGGACTAAAAGCCCTCCTCTCAGAATCGCGGTAACAAACCTCACCTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:32538655..32538754 26863196 MeRIP-seq:(Medium) rs1252557518 Functional Loss SNV dbSNP153 33..33 33 - - - 92016 RMVar_ID_92016 Human_SNP_ID_526060320 m1A Human chr13 + 32586514 32586513 32586514 GCAGGGCTGGCTGCGGAAGGGGAGGGGGGGGGAGAAGGCGATTGGATGCGGCGGCGGCGGCGGAT GCAGGGCTGGCTGCGGAAGGGGAGGGGGGGGG_GAAGGCGATTGGATGCGGCGGCGGCGGCGGAT GA G PDS5B Ensembl:ENSG00000083642 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:32586456..32586604 26863196 MeRIP-seq:(Medium) rs1391848811 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3944074,Human_RBP_ID_8792049,Human_RBP_ID_18417707,Human_RBP_ID_18978481,Human_RBP_ID_22919829,Human_RBP_ID_26324032,Human_RBP_ID_27807623 Human_Splice_Rec_1455441,Human_Splice_Rec_1455507,Human_Splice_Rec_1455511,Human_Splice_Rec_1455533,Human_Splice_Rec_1455597,Human_Splice_Rec_1455601 92017 RMVar_ID_92017 Human_SNP_ID_526060321 m1A Human chr13 + 32586514 32586514 32586514 GCAGGGCTGGCTGCGGAAGGGGAGGGGGGGGGAGAAGGCGATTGGATGCGGCGGCGGCGGCGGAT GCAGGGCTGGCTGCGGAAGGGGAGGGGGGGGGGGAAGGCGATTGGATGCGGCGGCGGCGGCGGAT A G PDS5B Ensembl:ENSG00000083642 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:32586456..32586604 26863196 MeRIP-seq:(Medium) rs879127242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944074,Human_RBP_ID_8792049,Human_RBP_ID_18417707,Human_RBP_ID_18978481,Human_RBP_ID_22919829,Human_RBP_ID_26324032,Human_RBP_ID_27807623 Human_Splice_Rec_1455441,Human_Splice_Rec_1455507,Human_Splice_Rec_1455511,Human_Splice_Rec_1455533,Human_Splice_Rec_1455597,Human_Splice_Rec_1455601 92018 RMVar_ID_92018 Human_SNP_ID_526076847 m1A Human chr13 - 32648689 32648689 32648689 AAAATAGATATAAACATTCTTAACAAACATAAATGGTAACCTTCCCCACCAACCAAAATTTGTAA AAAATAGATATAAACATTCTTAACAAACATAAGTGGTAACCTTCCCCACCAACCAAAATTTGTAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:32648686..32648850 26863196 MeRIP-seq:(Medium) rs1194313831 Functional Loss SNV dbSNP153 33..33 33 - - - 92019 RMVar_ID_92019 Human_SNP_ID_526108141 m1A Human chr13 + 32770494 32770494 32770494 AGCACCAGAGGAGGAGGAAGAAGAAGAAAGACAAAGTGGAAATACGGAACAGAAGTCCAAAAGCA AGCACCAGAGGAGGAGGAAGAAGAAGAAAGACGAAGTGGAAATACGGAACAGAAGTCCAAAAGCA A G PDS5B Ensembl:ENSG00000083642 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:32770443..32770513 26863196 MeRIP-seq:(Medium) rs766697845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37441,Human_RBP_ID_24543553,Human_RBP_ID_26324038,Human_RBP_ID_27807629 Human_Splice_Rec_1455501,Human_Splice_Rec_1455593,Human_Splice_Rec_1455617 RMVar_hsa_circ_42659,RMVar_hsa_circ_348942,RMVar_hsa_circ_96773,RMVar_hsa_circ_13704,RMVar_hsa_circ_162695,RMVar_hsa_circ_44487,RMVar_hsa_circ_162701,RMVar_hsa_circ_331661 92020 RMVar_ID_92020 Human_SNP_ID_526226146 m1A Human chr13 - 33248706 33248706 33248706 AAAGTGACTGGAGAAGTGGAGGAAGAAGAAAAATCAAAATATGGGAAGCAAAAGGGGAAAGGAAT AAAGTGACTGGAGAAGTGGAGGAAGAAGAAAATTCAAAATATGGGAAGCAAAAGGGGAAAGGAAT T A STARD13 Ensembl:ENSG00000133121 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:33248661..33248745 26863196 MeRIP-seq:(Medium) rs929070896 Functional Loss SNV dbSNP153 33..33 33 - - - 92021 RMVar_ID_92021 Human_SNP_ID_526226147 m1A Human chr13 - 33248706 33248706 33248706 AAAGTGACTGGAGAAGTGGAGGAAGAAGAAAAATCAAAATATGGGAAGCAAAAGGGGAAAGGAAT AAAGTGACTGGAGAAGTGGAGGAAGAAGAAAAGTCAAAATATGGGAAGCAAAAGGGGAAAGGAAT T C STARD13 Ensembl:ENSG00000133121 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:33248661..33248745 26863196 MeRIP-seq:(Medium) rs929070896 Functional Loss SNV dbSNP153 33..33 33 - - - 92022 RMVar_ID_92022 Human_SNP_ID_526250039 m1A Human chr13 + 33350609 33350609 33350609 GCCACGCGCGAGGACCGGGATGCCTGGCCACCAGAAACGCCGCGCTAGGTTATTAACCTCTGCGC GCCACGCGCGAGGACCGGGATGCCTGGCCACCCGAAACGCCGCGCTAGGTTATTAACCTCTGCGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:33350559..33350665 26863196 MeRIP-seq:(Medium) rs1487228817 Functional Loss SNV dbSNP153 33..33 33 - - - 92023 RMVar_ID_92023 Human_SNP_ID_526250040 m1A Human chr13 + 33350609 33350609 33350609 GCCACGCGCGAGGACCGGGATGCCTGGCCACCAGAAACGCCGCGCTAGGTTATTAACCTCTGCGC GCCACGCGCGAGGACCGGGATGCCTGGCCACCGGAAACGCCGCGCTAGGTTATTAACCTCTGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:33350559..33350665 26863196 MeRIP-seq:(Medium) rs1487228817 Functional Loss SNV dbSNP153 33..33 33 - - - 92024 RMVar_ID_92024 Human_SNP_ID_526250053 m1A Human chr13 - 33350629 33350629 33350629 AGGAGTAGAGGAGTTGGCGAGCGCAGAGGTTAATAACCTAGCGCGGCGTTTCTGGTGGCCAGGCA AGGAGTAGAGGAGTTGGCGAGCGCAGAGGTTAGTAACCTAGCGCGGCGTTTCTGGTGGCCAGGCA T C STARD13 Ensembl:ENSG00000133121 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:33350582..33350684 26863196 MeRIP-seq:(Medium) rs558234690 Functional Loss SNV dbSNP153 33..33 33 - - - 92025 RMVar_ID_92025 Human_SNP_ID_526250055 m1A Human chr13 - 33350635 33350635 33350635 TGGGAAAGGAGTAGAGGAGTTGGCGAGCGCAGAGGTTAATAACCTAGCGCGGCGTTTCTGGTGGC TGGGAAAGGAGTAGAGGAGTTGGCGAGCGCAGGGGTTAATAACCTAGCGCGGCGTTTCTGGTGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:33350585..33350674 26863196 MeRIP-seq:(Medium) rs1566154779 Functional Loss SNV dbSNP153 33..33 33 - - - 92026 RMVar_ID_92026 Human_SNP_ID_526363277 m1A Human chr13 + 33818198 33818198 33818198 AACTCGAGCTGCCATGAGCCTCTGGGTGGACAAGTATCGGCCCTGCTCCTTGGGACGGCTGGACT AACTCGAGCTGCCATGAGCCTCTGGGTGGACACGTATCGGCCCTGCTCCTTGGGACGGCTGGACT A C RFC3 Ensembl:ENSG00000133119 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:33818147..33818247 26863196 MeRIP-seq:(Medium) rs1398928860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_996207,Human_RBP_ID_1483064,Human_RBP_ID_1807442,Human_RBP_ID_4268351,Human_RBP_ID_8390714,Human_RBP_ID_17836342,Human_RBP_ID_18417711,Human_RBP_ID_18639067,Human_RBP_ID_23592505,Human_RBP_ID_27638359 Human_Splice_Rec_1456121,Human_Splice_Rec_1456137 92027 RMVar_ID_92027 Human_SNP_ID_526363286 m1A Human chr13 - 33818212 33818212 33818212 CTGCTCCTTGTGATAGTCCAGCCGTCCCAAGGAGCAGGGCCGATACTTGTCCACCCAGAGGCTCA CTGCTCCTTGTGATAGTCCAGCCGTCCCAAGGGGCAGGGCCGATACTTGTCCACCCAGAGGCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:33818119..33818300 26863196 MeRIP-seq:(Medium) rs763552185 Functional Loss SNV dbSNP153 33..33 33 - - - 92028 RMVar_ID_92028 Human_SNP_ID_526366365 m1A Human chr13 - 33829925 33829925 33829925 CACTTTAGATGTAGAATTGCAGCACAAGATCAATCTGCAGGTAGACATATATTTTTCCATGGTTC CACTTTAGATGTAGAATTGCAGCACAAGATCAGTCTGCAGGTAGACATATATTTTTCCATGGTTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:33829876..33829925 26863196 MeRIP-seq:(Medium) rs376123517 Functional Loss SNV dbSNP153 33..33 33 - - - 92029 RMVar_ID_92029 Human_SNP_ID_526386344 m1A Human chr13 - 33912543 33912543 33912543 TTCTGATTCCTCAGTTACAGCCTCTTGCCTCCAGGCCACTGCCCTGATGTTCCCCAGGCCTCCTT TTCTGATTCCTCAGTTACAGCCTCTTGCCTCCGGGCCACTGCCCTGATGTTCCCCAGGCCTCCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:33912498..33912662 26863196 MeRIP-seq:(Medium) rs1003888792 Functional Loss SNV dbSNP153 33..33 33 - - - 92030 RMVar_ID_92030 Human_SNP_ID_526386345 m1A Human chr13 + 33912546 33912546 33912546 GAGGCCTGGGGAACATCAGGGCAGTGGCCTGGAGGCAAGAGGCTGTAACTGAGGAATCAGAAGAG GAGGCCTGGGGAACATCAGGGCAGTGGCCTGGTGGCAAGAGGCTGTAACTGAGGAATCAGAAGAG A T RFC3 Ensembl:ENSG00000133119 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:33912498..33912729 26863196 MeRIP-seq:(Medium) rs538082570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6274378,Human_RBP_ID_12141222 92031 RMVar_ID_92031 Human_SNP_ID_526606263 m1A Human chr13 - 34801940 34801940 34801940 AGCCTAATGGATGTCAGGGTCAGTCTAAGTGAAAGCAAAGAGAGGCTGGGACGAGGGGTGCAAAG AGCCTAATGGATGTCAGGGTCAGTCTAAGTGAGAGCAAAGAGAGGCTGGGACGAGGGGTGCAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:34801893..34802003;chr13:34801894..34802011 26863196 MeRIP-seq:(Medium) rs1408825342 Functional Loss SNV dbSNP153 33..33 33 - - - 92032 RMVar_ID_92032 Human_SNP_ID_526641061 m1A Human chr13 - 34942345 34942345 34942345 TTGACGCTGCTGCCGCCGCTGCTACGGCCACCACTGTTGTTGTGAAGCCCCGACGCCGCCGCTCA TTGACGCTGCTGCCGCCGCTGCTACGGCCACCGCTGTTGTTGTGAAGCCCCGACGCCGCCGCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:34942298..34943029 26863196 MeRIP-seq:(Medium) rs749102299 Functional Loss SNV dbSNP153 33..33 33 - - - 92033 RMVar_ID_92033 Human_SNP_ID_526641062 m1A Human chr13 - 34942345 34942345 34942345 TTGACGCTGCTGCCGCCGCTGCTACGGCCACCACTGTTGTTGTGAAGCCCCGACGCCGCCGCTCA TTGACGCTGCTGCCGCCGCTGCTACGGCCACCCCTGTTGTTGTGAAGCCCCGACGCCGCCGCTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:34942298..34943029 26863196 MeRIP-seq:(Medium) rs749102299 Functional Loss SNV dbSNP153 33..33 33 - - - 92034 RMVar_ID_92034 Human_SNP_ID_526967925 m1A Human chr13 + 36317436 36317436 36317436 CAATCCCTTATTTCCGTGCCCCAACCTCTTATATCTCTGTGCCCCAATCCCTTATTTCTGTGCCC CAATCCCTTATTTCCGTGCCCCAACCTCTTATCTCTCTGTGCCCCAATCCCTTATTTCTGTGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:36317427..36317826 26863196 MeRIP-seq:(Medium) rs920361368 Functional Loss SNV dbSNP153 33..33 33 - - - 92035 RMVar_ID_92035 Human_SNP_ID_526968094 m1A Human chr13 - 36317979 36317979 36317979 AGATTTGGGACGAGTTGCACTGGGCACAGACTAGGAAGGGACTGATGTGTAAAAGAATGCCTGGA AGATTTGGGACGAGTTGCACTGGGCACAGACTGGGAAGGGACTGATGTGTAAAAGAATGCCTGGA T C SPART Ensembl:ENSG00000133104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:36317970..36318036;chr13:36317976..36318247 26863196 MeRIP-seq:(Medium) rs1369944458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87342,RMVar_hsa_circ_162840,RMVar_hsa_circ_91065,RMVar_hsa_circ_37859,RMVar_hsa_circ_38449,RMVar_hsa_circ_162842,RMVar_hsa_circ_326959 92036 RMVar_ID_92036 Human_SNP_ID_526968422 m1A Human chr13 + 36319193 36319193 36319193 AAGCACTCCTTTTTAGTTATCCCCACCTGCCCAGTTCCCTTATTAGGCTGAGACACTAACTAAAT AAGCACTCCTTTTTAGTTATCCCCACCTGCCCCGTTCCCTTATTAGGCTGAGACACTAACTAAAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:36319181..36319310 26863196 MeRIP-seq:(Medium) rs1459920667 Functional Loss SNV dbSNP153 33..33 33 - - - 92037 RMVar_ID_92037 Human_SNP_ID_526972448 m1A Human chr13 - 36335830 36335830 36335830 AGATAATTAAATATGTCTCCAATTTTGCAGAAATGGAGCAAGAGCCACAAAATGGAGAACCTGCT AGATAATTAAATATGTCTCCAATTTTGCAGAAGTGGAGCAAGAGCCACAAAATGGAGAACCTGCT T C SPART Ensembl:ENSG00000133104 Protein coding start codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:36335712..36336317 32194978 MeRIP-seq:(Medium) rs1288960337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4268658,Human_RBP_ID_22648016,Human_RBP_ID_27807904 Human_Splice_Rec_1457060,Human_Splice_Rec_1457076,Human_Splice_Rec_1457092,Human_Splice_Rec_1457126,Human_Splice_Rec_1457166,Human_Splice_Rec_1457174,Human_Splice_Rec_1457176 RMVar_hsa_circ_37859,RMVar_hsa_circ_317361,RMVar_hsa_circ_347279,RMVar_hsa_circ_162843,RMVar_hsa_circ_366415 92038 RMVar_ID_92038 Human_SNP_ID_526975008 m1A Human chr13 - 36346345 36346345 36346345 AAGCGCGCGCGCGAGGCCTTGGGAACCTCGGGACCGGCCCCCGGCGAGCGCAGCGGCGCCCAGTG AAGCGCGCGCGCGAGGCCTTGGGAACCTCGGGGCCGGCCCCCGGCGAGCGCAGCGGCGCCCAGTG T C SPART Ensembl:ENSG00000133104 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:36346224..36346404;chr13:36346179..36346440;chr13:36346193..36360672;chr13:36346201..36346463 26863196 MeRIP-seq:(Medium) rs772271103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118826,Human_RBP_ID_4268669,Human_RBP_ID_17115564,Human_RBP_ID_18410993 Human_Splice_Rec_1457123 92039 RMVar_ID_92039 Human_SNP_ID_527088741 m1A Human chr13 + 36819636 36819627 36819636 GAGGAGGCTGGGGAGGACGAGGCGGACCTGTTAGACACTTCGGACCCTCCGGGGGGAGGCGAGAG GAGGAGGCTGGGGAGGACGAGGCG_________GACACTTCGGACCCTCCGGGGGGAGGCGAGAG GGACCTGTTA G RFXAP Ensembl:ENSG00000133111 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:36819517..36819866;chr13:36819464..36819958;chr13:36819468..36819875 26863196 MeRIP-seq:(Medium) rs1566318853 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_6276469,Human_RBP_ID_9323608,Human_RBP_ID_12144967,Human_RBP_ID_18435193,Human_RBP_ID_22180217,Human_RBP_ID_26324320 92040 RMVar_ID_92040 Human_SNP_ID_527088743 m1A Human chr13 + 36819636 36819636 36819636 GAGGAGGCTGGGGAGGACGAGGCGGACCTGTTAGACACTTCGGACCCTCCGGGGGGAGGCGAGAG GAGGAGGCTGGGGAGGACGAGGCGGACCTGTTCGACACTTCGGACCCTCCGGGGGGAGGCGAGAG A C RFXAP Ensembl:ENSG00000133111 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:36819517..36819866;chr13:36819464..36819958;chr13:36819468..36819875 26863196 MeRIP-seq:(Medium) rs985061791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6276469,Human_RBP_ID_9323608,Human_RBP_ID_12144967,Human_RBP_ID_18435193,Human_RBP_ID_22180217,Human_RBP_ID_26324320 92041 RMVar_ID_92041 Human_SNP_ID_527101626 m1A Human chr13 + 36872767 36872767 36872767 GAGAACGCGTGGCTGGGTGAGGGAGGGAGTGCAGAGCACGGAGGCTGCTGGAAAGAGTCAGGATA GAGAACGCGTGGCTGGGTGAGGGAGGGAGTGCGGAGCACGGAGGCTGCTGGAAAGAGTCAGGATA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:36872717..36872912 26863196 MeRIP-seq:(Medium) rs1181535863 Functional Loss SNV dbSNP153 33..33 33 - - - 92042 RMVar_ID_92042 Human_SNP_ID_527103515 m1A Human chr13 - 36879551 36879551 36879551 AGGCAGTGGACTCTCTAGTGAAGAAGTTAAAGAAGAAGAAGGGAGCCATGGACGAGCTGGAGAGG AGGCAGTGGACTCTCTAGTGAAGAAGTTAAAGTAGAAGAAGGGAGCCATGGACGAGCTGGAGAGG T A SMAD9 Ensembl:ENSG00000120693 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:36879500..36879751 26863196 MeRIP-seq:(Medium) rs1482543614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4268781,Human_RBP_ID_5522293,Human_RBP_ID_17836950 RMVar_hsa_circ_301847,RMVar_hsa_circ_162850,RMVar_hsa_circ_319908,RMVar_hsa_circ_162851,RMVar_hsa_circ_35143 92043 RMVar_ID_92043 Human_SNP_ID_527103634 m1A Human chr13 + 36879863 36879863 36879863 AAGTGTGTTGACTTTCTCCTAAGCCCTTGAACAGGGTGGCCAACTCTGGAAAACACGACAAGACT AAGTGTGTTGACTTTCTCCTAAGCCCTTGAACGGGGTGGCCAACTCTGGAAAACACGACAAGACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:36879814..36920154 26863196 MeRIP-seq:(Medium) rs1245810577 Functional Loss SNV dbSNP153 33..33 33 - - - 92044 RMVar_ID_92044 Human_SNP_ID_527134072 m1A Human chr13 + 37000822 37000822 37000822 ACGCGCGGGCGGGAAGATGGCGGCTGGGTTCAAGTGAGTGTTGGCGGGTGGCGGGTAGAGTTCTG ACGCGCGGGCGGGAAGATGGCGGCTGGGTTCAGGTGAGTGTTGGCGGGTGGCGGGTAGAGTTCTG A G EXOSC8 Ensembl:ENSG00000120699 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control chr13:37000776..37000875;chr13:37000751..37000850;chr13:37000801..37000894 26863410 MeRIP-seq:(Medium) rs550092596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276959,Human_RBP_ID_19062111 Human_Splice_Rec_1457381,Human_Splice_Rec_1457397,Human_Splice_Rec_1457417,Human_Splice_Rec_1457435 92045 RMVar_ID_92045 Human_SNP_ID_527134074 m1A Human chr13 - 37000824 37000824 37000824 TACAGAACTCTACCCGCCACCCGCCAACACTCACTTGAACCCAGCCGCCATCTTCCCGCCCGCGC TACAGAACTCTACCCGCCACCCGCCAACACTCGCTTGAACCCAGCCGCCATCTTCCCGCCCGCGC T C lnc-ALG5-2 RNACentral:URS00008B699F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:37000707..37000919;chr13:37000660..37001509;chr13:37000703..37001509 26863196 MeRIP-seq:(Medium) rs1403422168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12146747 92046 RMVar_ID_92046 Human_SNP_ID_527134079 m1A Human chr13 - 37000830 37000830 37000830 CCAGGGTACAGAACTCTACCCGCCACCCGCCAACACTCACTTGAACCCAGCCGCCATCTTCCCGC CCAGGGTACAGAACTCTACCCGCCACCCGCCAGCACTCACTTGAACCCAGCCGCCATCTTCCCGC T C lnc-ALG5-2 RNACentral:URS00008B699F lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:37000827..37001056 26863196 MeRIP-seq:(Medium) rs200292064 Functional Loss SNV dbSNP153 33..33 33 - - - 92047 RMVar_ID_92047 Human_SNP_ID_527134116 m1A Human chr13 + 37000871 37000871 37000871 GGCGGGTAGAGTTCTGTACCCTGGCGGACGGCAGCTTCCTTTAACTCTTAGCTGGGATTCTCTCA GGCGGGTAGAGTTCTGTACCCTGGCGGACGGCGGCTTCCTTTAACTCTTAGCTGGGATTCTCTCA A G EXOSC8 Ensembl:ENSG00000120699 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:37000866..37000999 32194978 MeRIP-seq:(Medium) rs1310418292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5350814,Human_RBP_ID_6277222,Human_RBP_ID_12146750,Human_RBP_ID_19062111,Human_RBP_ID_22042165,Human_RBP_ID_22180250,Human_RBP_ID_22354858,Human_RBP_ID_23593653 92048 RMVar_ID_92048 Human_SNP_ID_527134117 m1A Human chr13 + 37000871 37000871 37000871 GGCGGGTAGAGTTCTGTACCCTGGCGGACGGCAGCTTCCTTTAACTCTTAGCTGGGATTCTCTCA GGCGGGTAGAGTTCTGTACCCTGGCGGACGGCTGCTTCCTTTAACTCTTAGCTGGGATTCTCTCA A T EXOSC8 Ensembl:ENSG00000120699 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:37000866..37000999 32194978 MeRIP-seq:(Medium) rs1310418292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5350814,Human_RBP_ID_6277222,Human_RBP_ID_12146750,Human_RBP_ID_19062111,Human_RBP_ID_22042165,Human_RBP_ID_22180250,Human_RBP_ID_22354858,Human_RBP_ID_23593653 92049 RMVar_ID_92049 Human_SNP_ID_527134125 m1A Human chr13 - 37000886 37000885 37000887 GGGTCGGCCTCCAGGTGAGAGAATCCCAGCTAAGAGTTAAAGGAAGCTGCCGTCCGCCAGGGTAC GGGTCGGCCTCCAGGTGAGAGAATCCCAGCT__GAGTTAAAGGAAGCTGCCGTCCGCCAGGGTAC CTT C lnc-ALG5-2 RNACentral:URS00008B699F lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:37000841..37000983 26863196 MeRIP-seq:(Medium) rs1212820538 Functional Loss DEL dbSNP153 32..33 33 - - - 92050 RMVar_ID_92050 Human_SNP_ID_527134135 m1A Human chr13 + 37000915 37000912 37000915 CTCTTAGCTGGGATTCTCTCACCTGGAGGCCGACCCCGTTGGGGTGCCATTTCCTTCCTCGTCGA CTCTTAGCTGGGATTCTCTCACCTGGAGGC___CCCCGTTGGGGTGCCATTTCCTTCCTCGTCGA CCGA C EXOSC8 Ensembl:ENSG00000120699 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr13:37000869..37001009;chr13:37000833..37001032 26863196 MeRIP-seq:(Medium) rs1263683186 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5350815,Human_RBP_ID_22354858 92051 RMVar_ID_92051 Human_SNP_ID_527134559 m1A Human chr13 - 37002425 37002424 37002426 TATACCTATTACATATTTTACACATCTATCACAAGTTTTACACACACATTAAATGTTACTTCAAA TATACCTATTACATATTTTACACATCTATCA__AGTTTTACACACACATTAAATGTTACTTCAAA TTG T lnc-ALG5-2 RNACentral:URS00008B699F lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:37002419..37002520 26863410 MeRIP-seq:(Medium) rs1350113021 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3428492 92052 RMVar_ID_92052 Human_SNP_ID_527134560 m1A Human chr13 - 37002425 37002425 37002425 TATACCTATTACATATTTTACACATCTATCACAAGTTTTACACACACATTAAATGTTACTTCAAA TATACCTATTACATATTTTACACATCTATCACGAGTTTTACACACACATTAAATGTTACTTCAAA T C lnc-ALG5-2 RNACentral:URS00008B699F lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:37002419..37002520 26863410 MeRIP-seq:(Medium) rs1304279958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3428492 92053 RMVar_ID_92053 Human_SNP_ID_527134575 m1A Human chr13 + 37002478 37002478 37002478 GTAATAGGTATAATCTATTTTTATATAAACATATTTATTTAGAAAGAGAACTGCCGTCCTGATGG GTAATAGGTATAATCTATTTTTATATAAACATGTTTATTTAGAAAGAGAACTGCCGTCCTGATGG A G EXOSC8 Ensembl:ENSG00000120699 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:37002476..37002550 32194978 MeRIP-seq:(Medium) rs1386675479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6277237,Human_RBP_ID_25045916 Human_Splice_Rec_1457373,Human_Splice_Rec_1457383,Human_Splice_Rec_1457403,Human_Splice_Rec_1457421,Human_Splice_Rec_1457439,Human_Splice_Rec_1457455,Human_Splice_Rec_1457459,Human_Splice_Rec_1457475,Human_Splice_Rec_1457489 RMVar_hsa_circ_377804 92054 RMVar_ID_92054 Human_SNP_ID_527146295 m1A Human chr13 - 37051559 37051559 37051559 CTTTTCAGTACTGTAAGATTGATGTTAAAGGCATGGTGTTCACCCCACTTCATCAGCGTACATAA CTTTTCAGTACTGTAAGATTGATGTTAAAGGCGTGGTGTTCACCCCACTTCATCAGCGTACATAA T C SUPT20H Ensembl:ENSG00000102710 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:37051440..37051659 26863196 MeRIP-seq:(Medium) rs1180620160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1808282,Human_RBP_ID_4276593,Human_RBP_ID_18639642,Human_RBP_ID_26807701,Human_RBP_ID_27638836 Human_Splice_Rec_1457524,Human_Splice_Rec_1457525,Human_Splice_Rec_1457572,Human_Splice_Rec_1457573,Human_Splice_Rec_1457622,Human_Splice_Rec_1457623,Human_Splice_Rec_1457666,Human_Splice_Rec_1457667,Human_Splice_Rec_1457714,Human_Splice_Rec_1457715,Human_Splice_Rec_1457786,Human_Splice_Rec_1457787,Human_Splice_Rec_1457835,Human_Splice_Rec_1457882,Human_Splice_Rec_1457883,Human_Splice_Rec_1457941,Human_Splice_Rec_1458002,Human_Splice_Rec_1458003,Human_Splice_Rec_1458024,Human_Splice_Rec_1458025,Human_Splice_Rec_1458040,Human_Splice_Rec_1458041,Human_Splice_Rec_1458056,Human_Splice_Rec_1458057,Human_Splice_Rec_1458078 Human_miRNA_ID_2870030,Human_miRNA_ID_2870031,Human_miRNA_ID_2870032 RMVar_hsa_circ_14313,RMVar_hsa_circ_341021,RMVar_hsa_circ_330744,RMVar_hsa_circ_162862,RMVar_hsa_circ_102021,RMVar_hsa_circ_162864,RMVar_hsa_circ_61261,RMVar_hsa_circ_34171,RMVar_hsa_circ_271677,RMVar_hsa_circ_314163,RMVar_hsa_circ_322896,RMVar_hsa_circ_162867,RMVar_hsa_circ_162870,RMVar_hsa_circ_19321,RMVar_hsa_circ_301095,RMVar_hsa_circ_162871,RMVar_hsa_circ_320774 92055 RMVar_ID_92055 Human_SNP_ID_527148447 m1A Human chr13 + 37059610 37059610 37059610 GCTAGGCCCCAAGACGGCGCCGCCTGCTCGGCAGCAAAGCCCACCCGCCCCGTCGGCGGCTCAGT GCTAGGCCCCAAGACGGCGCCGCCTGCTCGGCGGCAAAGCCCACCCGCCCCGTCGGCGGCTCAGT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr13:37059400..37059675;chr13:37059416..37059675 26863196 MeRIP-seq:(Medium) rs980865408 Functional Loss SNV dbSNP153 33..33 33 - - - 92056 RMVar_ID_92056 Human_SNP_ID_527148448 m1A Human chr13 + 37059613 37059613 37059613 AGGCCCCAAGACGGCGCCGCCTGCTCGGCAGCAAAGCCCACCCGCCCCGTCGGCGGCTCAGTGCT AGGCCCCAAGACGGCGCCGCCTGCTCGGCAGCGAAGCCCACCCGCCCCGTCGGCGGCTCAGTGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr13:37059500..37059675;chr13:37059441..37059652 26863196 MeRIP-seq:(Medium) rs1003087616 Functional Loss SNV dbSNP153 33..33 33 - - - 92057 RMVar_ID_92057 Human_SNP_ID_527462960 m1A Human chr13 + 38349917 38349917 38349917 GTTGTCGTGTGTTCTGGATTCATTCCGGCACCACCATGTAAGTGTTTGCTTACCGACTGCCATAA GTTGTCGTGTGTTCTGGATTCATTCCGGCACCGCCATGTAAGTGTTTGCTTACCGACTGCCATAA A G UFM1 Ensembl:ENSG00000120686 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:38349879..38350232 26863196 MeRIP-seq:(Medium) rs1424329031 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4276595,Human_RBP_ID_5492676 Human_Splice_Rec_1458599,Human_Splice_Rec_1458603,Human_Splice_Rec_1458613,Human_Splice_Rec_1458623 92058 RMVar_ID_92058 Human_SNP_ID_527462963 m1A Human chr13 + 38349920 38349920 38349920 GTCGTGTGTTCTGGATTCATTCCGGCACCACCATGTAAGTGTTTGCTTACCGACTGCCATAATTC GTCGTGTGTTCTGGATTCATTCCGGCACCACCGTGTAAGTGTTTGCTTACCGACTGCCATAATTC A G UFM1 Ensembl:ENSG00000120686 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:38349897..38349982 26863196 MeRIP-seq:(Medium) rs1172508646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276595,Human_RBP_ID_5492676 Human_Splice_Rec_1458599,Human_Splice_Rec_1458603,Human_Splice_Rec_1458613,Human_Splice_Rec_1458623 92059 RMVar_ID_92059 Human_SNP_ID_527465798 m1A Human chr13 + 38361776 38361776 38361776 AGATCACCAGGCTTCTATTAAGGAGGAAAGCAACAGAGGAAACAGTGAAGGGGAACAGAAGGGGG AGATCACCAGGCTTCTATTAAGGAGGAAAGCAGCAGAGGAAACAGTGAAGGGGAACAGAAGGGGG A G UFM1 Ensembl:ENSG00000120686 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:38361726..38361900 26863196 MeRIP-seq:(Medium) rs1485221553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6278360,Human_RBP_ID_8180653,Human_RBP_ID_12148458,Human_RBP_ID_26425335,Human_RBP_ID_27638916 Human_miRNA_ID_1343547,Human_miRNA_ID_2648168,Human_miRNA_ID_2670765,Human_miRNA_ID_3101416 RMVar_hsa_circ_125783,RMVar_hsa_circ_162879 92060 RMVar_ID_92060 Human_SNP_ID_527624766 m1A Human chr13 - 39013232 39013232 39013232 TCTCCAGCTTGAGTACTCCTTTAAATGGTTCAAATCCTCTTTCCTCTATTTCCCTTCCACCACAT TCTCCAGCTTGAGTACTCCTTTAAATGGTTCACATCCTCTTTCCTCTATTTCCCTTCCACCACAT T G PROSER1 Ensembl:ENSG00000120685 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_17244731,Human_RBP_ID_17359646,Human_RBP_ID_17476457,Human_RBP_ID_18936333,Human_RBP_ID_27427693 Human_miRNA_ID_822419,Human_miRNA_ID_2350397,Human_miRNA_ID_3094864 RMVar_hsa_circ_162885,RMVar_hsa_circ_119274,RMVar_hsa_circ_162886 92061 RMVar_ID_92061 Human_SNP_ID_527624948 m1A Human chr13 + 39013681 39013675 39013681 ACCCTGGAGTGGAAGTCCTCTGTGGGGTAGGGATGGCTGATGGGGCATAGCACTTGTTAGGGGCT ACCCTGGAGTGGAAGTCCTCTGTGGGG______TGGCTGATGGGGCATAGCACTTGTTAGGGGCT GTAGGGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:39013580..39013694 26863196 MeRIP-seq:(Medium) rs1566021935 Functional Loss DEL dbSNP153 28..33 33 - - - 92062 RMVar_ID_92062 Human_SNP_ID_527625185 m1A Human chr13 - 39014189 39014189 39014189 CTGCACCTGTTACATCCATCCACAGTACAACCACCACTCCTGTTCCTTCCATTTTTTCTGGCCTA CTGCACCTGTTACATCCATCCACAGTACAACCGCCACTCCTGTTCCTTCCATTTTTTCTGGCCTA T C PROSER1 Ensembl:ENSG00000120685 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:39014140..39014338 26863196 MeRIP-seq:(Medium) rs776865093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8391560,Human_RBP_ID_17244754,Human_RBP_ID_17476474 Human_miRNA_ID_1971004 RMVar_hsa_circ_162885,RMVar_hsa_circ_119274,RMVar_hsa_circ_162886 92063 RMVar_ID_92063 Human_SNP_ID_527625224 m1A Human chr13 - 39014276 39014276 39014276 TGTTCCCAGGGCAGGTCTCCTCAGCCGTTCACACACCTCAGCCATCAATACCAAACCCAACAGTT TGTTCCCAGGGCAGGTCTCCTCAGCCGTTCACGCACCTCAGCCATCAATACCAAACCCAACAGTT T C PROSER1 Ensembl:ENSG00000120685 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:39014177..39014327 26863196 MeRIP-seq:(Medium) rs1330940179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17244756,Human_RBP_ID_17359667,Human_RBP_ID_17476477 RMVar_hsa_circ_162885,RMVar_hsa_circ_119274,RMVar_hsa_circ_162886 92064 RMVar_ID_92064 Human_SNP_ID_527631479 m1A Human chr13 - 39038024 39038024 39038024 TGAGTTTACTTGGGCGCGACTGGCTTTATTGTAGGTCCCCATGAGCTGGTGGGGGCTGTAGGGGT TGAGTTTACTTGGGCGCGACTGGCTTTATTGTTGGTCCCCATGAGCTGGTGGGGGCTGTAGGGGT T A PROSER1 Ensembl:ENSG00000120685 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:39037974..39038062 26863196 MeRIP-seq:(Medium) rs1043353058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276780,Human_RBP_ID_12150567,Human_RBP_ID_17837344,Human_RBP_ID_19855218 92065 RMVar_ID_92065 Human_SNP_ID_527631486 m1A Human chr13 - 39038038 39038038 39038038 TGGCGGCGCAGTGTTGAGTTTACTTGGGCGCGACTGGCTTTATTGTAGGTCCCCATGAGCTGGTG TGGCGGCGCAGTGTTGAGTTTACTTGGGCGCGGCTGGCTTTATTGTAGGTCCCCATGAGCTGGTG T C PROSER1 Ensembl:ENSG00000120685 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:39037876..39038059 26863196 MeRIP-seq:(Medium) rs1281158872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1483908,Human_RBP_ID_5462770,Human_RBP_ID_5493113,Human_RBP_ID_6279424,Human_RBP_ID_12150567,Human_RBP_ID_17837344,Human_RBP_ID_23594216,Human_RBP_ID_27639047 92066 RMVar_ID_92066 Human_SNP_ID_527760994 m1A Human chr13 + 39583855 39583855 39583855 CCACTGCCTCCCTCTCCAGCTTCACCTGACCCATCCTCCCTCGTGTCCTCCGGTCTAGTGTGCCT CCACTGCCTCCCTCTCCAGCTTCACCTGACCCGTCCTCCCTCGTGTCCTCCGGTCTAGTGTGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:39583820..39583903 26863196 MeRIP-seq:(Medium) rs1188238540 Functional Loss SNV dbSNP153 33..33 33 - - - 92067 RMVar_ID_92067 Human_SNP_ID_527765433 m1A Human chr13 + 39602958 39602958 39602958 GCACACACAACTTGCTGTCTTTCTCGGGCGGGAACATCCACGGGAAACCGGACCGTCCTGCCCTT GCACACACAACTTGCTGTCTTTCTCGGGCGGGTACATCCACGGGAAACCGGACCGTCCTGCCCTT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:39601351..39603091 32194978 MeRIP-seq:(Medium) rs950778619 Functional Loss SNV dbSNP153 33..33 33 - - - 92068 RMVar_ID_92068 Human_SNP_ID_527765495 m1A Human chr13 - 39603141 39603141 39603141 GCGTGCGATCCCCGGCGCCCGCGCGCGCCCACAGCGCTCCGCCAGAGCTGCCGCCGCGGACTCGC GCGTGCGATCCCCGGCGCCCGCGCGCGCCCACGGCGCTCCGCCAGAGCTGCCGCCGCGGACTCGC T C LHFPL6 Ensembl:ENSG00000183722 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:39603059..39603171 26863196 MeRIP-seq:(Medium) rs916794457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4269394 92069 RMVar_ID_92069 Human_SNP_ID_527778428 m1A Human chr13 - 39655854 39655854 39655854 CGGTTACCTTGTCGTTGTCCAGCCGCGTCTCCAGGATCTTATGCAGCTTGCGCGACAGCGGGTTG CGGTTACCTTGTCGTTGTCCAGCCGCGTCTCCGGGATCTTATGCAGCTTGCGCGACAGCGGGTTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:39655735..39655853 26863196 MeRIP-seq:(Medium) rs770003167 Functional Loss SNV dbSNP153 33..33 33 - - - 92070 RMVar_ID_92070 Human_SNP_ID_527788204 m1A Human chr13 + 39696593 39696592 39696593 AGCTTGCATTTTGGAGGACTAGAAAGAAAACCAGGAATTGGAGTGTAGTGAATTGGAAGGAGTAG AGCTTGCATTTTGGAGGACTAGAAAGAAAACC_GGAATTGGAGTGTAGTGAATTGGAAGGAGTAG CA C COG6 Ensembl:ENSG00000133103 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:39696562..39696695 26863196 MeRIP-seq:(Medium) rs1337165051 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_1095,RMVar_hsa_circ_44749,RMVar_hsa_circ_305117,RMVar_hsa_circ_286224,RMVar_hsa_circ_162898,RMVar_hsa_circ_162900,RMVar_hsa_circ_280323,RMVar_hsa_circ_162899,RMVar_hsa_circ_162901,RMVar_hsa_circ_162903,RMVar_hsa_circ_305207,RMVar_hsa_circ_306919,RMVar_hsa_circ_265521,RMVar_hsa_circ_162902 92071 RMVar_ID_92071 Human_SNP_ID_528022870 m1A Human chr13 + 40666250 40666250 40666250 CCCCCGCCCCTCCCCCAGCCGCAGGAGAGCCAAGAGGGGGAGAACGCAGCACTGGGGGCGGACGG CCCCCGCCCCTCCCCCAGCCGCAGGAGAGCCAGGAGGGGGAGAACGCAGCACTGGGGGCGGACGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:40666226..40666365 26863196 MeRIP-seq:(Medium) rs991694850 Functional Loss SNV dbSNP153 33..33 33 - - - 92072 RMVar_ID_92072 Human_SNP_ID_528022934 m1A Human chr13 - 40666430 40666430 40666430 GGCTCTGGCCGGCCGTCCAGTCCGTGCGGCGGACCCCGAGGAGCCTCGATGTGGATGGCCCCGCG GGCTCTGGCCGGCCGTCCAGTCCGTGCGGCGGGCCCCGAGGAGCCTCGATGTGGATGGCCCCGCG T C FOXO1 Ensembl:ENSG00000150907 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:40666189..40666590 26863196 MeRIP-seq:(Medium) rs1458240726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276448 92073 RMVar_ID_92073 Human_SNP_ID_528022954 m1A Human chr13 - 40666492 40666492 40666492 TCCGTCCTTCCGTCCGCGGCCCTGTCAGCTGGAGCGCGGCGCAGGCTCTGCCCCGGCCCGGCGGC TCCGTCCTTCCGTCCGCGGCCCTGTCAGCTGGGGCGCGGCGCAGGCTCTGCCCCGGCCCGGCGGC T C FOXO1 Ensembl:ENSG00000150907 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:40666397..40666547 26863410 MeRIP-seq:(Medium) rs1379556959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276448,Human_RBP_ID_9367894 92074 RMVar_ID_92074 Human_SNP_ID_528045590 m1A Human chr13 - 40758989 40758989 40758989 GAGCTGCTGAGCCAGCTCCAGCAGCATGAGGAAGAGTCAAGGGCACAGAGAGATGCAAAGCGACC GAGCTGCTGAGCCAGCTCCAGCAGCATGAGGAGGAGTCAAGGGCACAGAGAGATGCAAAGCGACC T C MRPS31 Ensembl:ENSG00000102738 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:40757004..40759037 32194978 MeRIP-seq:(Medium) rs202016797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1459309 RMVar_hsa_circ_272531,RMVar_hsa_circ_327728,RMVar_hsa_circ_96833,RMVar_hsa_circ_162917,RMVar_hsa_circ_128088,RMVar_hsa_circ_8891,RMVar_hsa_circ_162916,RMVar_hsa_circ_365146,RMVar_hsa_circ_284478,RMVar_hsa_circ_364784,RMVar_hsa_circ_162918 92075 RMVar_ID_92075 Human_SNP_ID_528047433 m1A Human chr13 - 40766923 40766923 40766923 TGAGGAGACTTCCAAGGAGACTTCAGAGAGCCAAGACAGTGAAAAGGAAAATACGAAAAAAGACT TGAGGAGACTTCCAAGGAGACTTCAGAGAGCCGAGACAGTGAAAAGGAAAATACGAAAAAAGACT T C MRPS31 Ensembl:ENSG00000102738 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:40766873..40770786 32194978 MeRIP-seq:(Medium) rs201183404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1484027,Human_RBP_ID_8391797,Human_RBP_ID_12155423 RMVar_hsa_circ_327728,RMVar_hsa_circ_96833,RMVar_hsa_circ_162917,RMVar_hsa_circ_128088,RMVar_hsa_circ_8891,RMVar_hsa_circ_162916,RMVar_hsa_circ_336975 92076 RMVar_ID_92076 Human_SNP_ID_528048508 m1A Human chr13 - 40771061 40771061 40771061 CCCGCCACCCTTTGTCCTCTGGAAGCCCGGAGACATCAGCGGCTGCGATTATGCTACTCACTGTT CCCGCCACCCTTTGTCCTCTGGAAGCCCGGAGGCATCAGCGGCTGCGATTATGCTACTCACTGTT T C MRPS31 Ensembl:ENSG00000102738 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:40770934..40771074 32194978 MeRIP-seq:(Medium) rs1439577746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_435943,Human_RBP_ID_812385,Human_RBP_ID_9367895,Human_RBP_ID_26324053 Human_Splice_Rec_1459305 RMVar_hsa_circ_96833,RMVar_hsa_circ_162917,RMVar_hsa_circ_128088,RMVar_hsa_circ_162916 92077 RMVar_ID_92077 Human_SNP_ID_528048525 m1A Human chr13 + 40771095 40771095 40771095 TCCGGGCTTCCAGAGGACAAAGGGTGGCGGGAAAGGGGGCGAAGAGGTAGGAACGTCGAGACTCT TCCGGGCTTCCAGAGGACAAAGGGTGGCGGGAGAGGGGGCGAAGAGGTAGGAACGTCGAGACTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:40771047..40771141 26863196 MeRIP-seq:(Medium) rs1231647777 Functional Loss SNV dbSNP153 33..33 33 - - - 92078 RMVar_ID_92078 Human_SNP_ID_528052848 m1A Human chr13 - 40789639 40789639 40789639 GCGCTCACCGCCGCGCCGGCGTGGCCGCGTCCAGCTCAGGCTCCGCCGCCCGCTCTCGGCTCCGG GCGCTCACCGCCGCGCCGGCGTGGCCGCGTCCGGCTCAGGCTCCGCCGCCCGCTCTCGGCTCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:40789445..40793222;chr13:40789465..40793212 26863196 MeRIP-seq:(Medium) rs1292571563 Functional Loss SNV dbSNP153 33..33 33 - - - 92079 RMVar_ID_92079 Human_SNP_ID_528118126 m1A Human chr13 + 41060883 41060883 41060883 GTGCCTCTGCCTCCTTCGCCGCACCTCTCGCCACCGCCGCCTCTGCGCTACTGAAGCTGCTGCTG GTGCCTCTGCCTCCTTCGCCGCACCTCTCGCCGCCGCCGCCTCTGCGCTACTGAAGCTGCTGCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:41019268..41060968 26863196 MeRIP-seq:(Medium) rs985850175 Functional Loss SNV dbSNP153 33..33 33 - - - 92080 RMVar_ID_92080 Human_SNP_ID_528118183 m1A Human chr13 - 41060914 41060914 41060914 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCTTCAGTAGCGCAGAGGCGGCGGTG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCTTCAGTAGCGCAGAGGCGGCGGTG T C ELF1 Ensembl:ENSG00000120690 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:41060888..41060965 26863196 MeRIP-seq:(Medium) rs867278669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5522298 Human_Splice_Rec_1459489 92081 RMVar_ID_92081 Human_SNP_ID_528118486 m1A Human chr13 + 41061265 41061254 41061265 AGGCGGCGCGCTGAGCTCCTTGGCCTTGAGCCAGCGAGCCTAGAAGGAGGATGGAGGTTTTGGGC AGGCGGCGCGCTGAGCTCCTTG___________GCGAGCCTAGAAGGAGGATGGAGGTTTTGGGC GGCCTTGAGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:41061214..41061354 26863196 MeRIP-seq:(Medium) rs1428195196 Functional Loss DEL dbSNP153 23..33 33 - - - 92082 RMVar_ID_92082 Human_SNP_ID_528118510 m1A Human chr13 + 41061301 41061301 41061301 AGCCTAGAAGGAGGATGGAGGTTTTGGGCCCCAGGGGAGGACACAGAGACGGCGGGATGGCGCAG AGCCTAGAAGGAGGATGGAGGTTTTGGGCCCCGGGGGAGGACACAGAGACGGCGGGATGGCGCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:41061256..41061354 26863410 MeRIP-seq:(Medium) rs1003095194 Functional Loss SNV dbSNP153 33..33 33 - - - 92083 RMVar_ID_92083 Human_SNP_ID_528118526 m1A Human chr13 + 41061332 41061332 41061332 CAGGGGAGGACACAGAGACGGCGGGATGGCGCAGGGACTTGAGGCTTGAGATCCCGTCCTTCAGC CAGGGGAGGACACAGAGACGGCGGGATGGCGCGGGGACTTGAGGCTTGAGATCCCGTCCTTCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:41060825..41061390;chr13:41061140..41061390;chr13:41061190..41061472 26863196 MeRIP-seq:(Medium) rs1339090434 Functional Loss SNV dbSNP153 33..33 33 - - - 92084 RMVar_ID_92084 Human_SNP_ID_528119081 m1A Human chr13 + 41062588 41062588 41062588 ATTTCAAACTTTAAAAACTGTAAAGCATGCAGAATTTAACCTTTTTTAAGTTTTACATGAGCTTA ATTTCAAACTTTAAAAACTGTAAAGCATGCAGTATTTAACCTTTTTTAAGTTTTACATGAGCTTA A T WBP4 Ensembl:ENSG00000120688 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:41062585..41062659 26863196 MeRIP-seq:(Medium) rs1316052713 Functional Loss SNV dbSNP153 33..33 33 - - - 92085 RMVar_ID_92085 Human_SNP_ID_528119803 m1A Human chr13 + 41065227 41065227 41065227 AAGAAGAAAAGGCATCAAAGGAGTTTGCTGCAATGGAGGCAGCTGCCCTGAAAGCATACCAAGAG AAGAAGAAAAGGCATCAAAGGAGTTTGCTGCAGTGGAGGCAGCTGCCCTGAAAGCATACCAAGAG A G WBP4 Ensembl:ENSG00000120688 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:41065098..41065252 26863196 MeRIP-seq:(Medium) rs920912586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_436008,Human_RBP_ID_9367465,Human_RBP_ID_18978823,Human_RBP_ID_26324056,Human_RBP_ID_27807657 Human_Splice_Rec_1459496,Human_Splice_Rec_1459497 RMVar_hsa_circ_59098,RMVar_hsa_circ_361111,RMVar_hsa_circ_351581,RMVar_hsa_circ_365836,RMVar_hsa_circ_298165,RMVar_hsa_circ_162932,RMVar_hsa_circ_44406 92086 RMVar_ID_92086 Human_SNP_ID_528136939 m1A Human chr13 + 41132664 41132664 41132664 CCCATTTACTGAATTCAACCCTACCCCGCAGAACCGCCTCCCGTTATCGTTTAGACAGTGGCTGA CCCATTTACTGAATTCAACCCTACCCCGCAGAGCCGCCTCCCGTTATCGTTTAGACAGTGGCTGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:41132614..41132746 26863196 MeRIP-seq:(Medium) rs9566703 Functional Loss SNV dbSNP153 33..33 33 - - - 92087 RMVar_ID_92087 Human_SNP_ID_528136940 m1A Human chr13 + 41132664 41132664 41132664 CCCATTTACTGAATTCAACCCTACCCCGCAGAACCGCCTCCCGTTATCGTTTAGACAGTGGCTGA CCCATTTACTGAATTCAACCCTACCCCGCAGATCCGCCTCCCGTTATCGTTTAGACAGTGGCTGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:41132614..41132746 26863196 MeRIP-seq:(Medium) rs9566703 Functional Loss SNV dbSNP153 33..33 33 - - - 92088 RMVar_ID_92088 Human_SNP_ID_528147961 m1A Human chr13 - 41183357 41183357 41183357 TTGAACCGGGGAGGAGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGAT TTGAACCGGGGAGGAGGAGGTTGCAGTGAGCCTAGATCACGCCACTGCACTCCAGCCTGGGCGAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:41183354..41183481 26863196 MeRIP-seq:(Medium) rs111605029 Functional Loss SNV dbSNP153 33..33 33 - - - 92089 RMVar_ID_92089 Human_SNP_ID_528163055 m1A Human chr13 - 41250266 41250261 41250266 TAAAAAGAGGATTCAAGATAATCAGAAAAAGGATGAGGACAGTAAAATATTATGGAAGCAAAAGA TAAAAAGAGGATTCAAGATAATCAGAAAAAGG_____GACAGTAAAATATTATGGAAGCAAAAGA CCTCAT C MTRF1 Ensembl:ENSG00000120662 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:41250216..41250341 26863196 MeRIP-seq:(Medium) rs1232835045 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_12156581 RMVar_hsa_circ_311761,RMVar_hsa_circ_332064,RMVar_hsa_circ_86304,RMVar_hsa_circ_329534,RMVar_hsa_circ_351806,RMVar_hsa_circ_55310,RMVar_hsa_circ_162937,RMVar_hsa_circ_360621,RMVar_hsa_circ_120203,RMVar_hsa_circ_278218,RMVar_hsa_circ_117038,RMVar_hsa_circ_162940,RMVar_hsa_circ_162941,RMVar_hsa_circ_162942,RMVar_hsa_circ_162939,RMVar_hsa_circ_162943,RMVar_hsa_circ_73864,RMVar_hsa_circ_86972,RMVar_hsa_circ_287202,RMVar_hsa_circ_67400,RMVar_hsa_circ_162944 92090 RMVar_ID_92090 Human_SNP_ID_528163056 m1A Human chr13 - 41250266 41250266 41250266 TAAAAAGAGGATTCAAGATAATCAGAAAAAGGATGAGGACAGTAAAATATTATGGAAGCAAAAGA TAAAAAGAGGATTCAAGATAATCAGAAAAAGGGTGAGGACAGTAAAATATTATGGAAGCAAAAGA T C MTRF1 Ensembl:ENSG00000120662 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:41250216..41250341 26863196 MeRIP-seq:(Medium) rs562423858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12156581 RMVar_hsa_circ_311761,RMVar_hsa_circ_332064,RMVar_hsa_circ_86304,RMVar_hsa_circ_329534,RMVar_hsa_circ_351806,RMVar_hsa_circ_55310,RMVar_hsa_circ_162937,RMVar_hsa_circ_360621,RMVar_hsa_circ_120203,RMVar_hsa_circ_278218,RMVar_hsa_circ_117038,RMVar_hsa_circ_162940,RMVar_hsa_circ_162941,RMVar_hsa_circ_162942,RMVar_hsa_circ_162939,RMVar_hsa_circ_162943,RMVar_hsa_circ_73864,RMVar_hsa_circ_86972,RMVar_hsa_circ_287202,RMVar_hsa_circ_67400,RMVar_hsa_circ_162944 92091 RMVar_ID_92091 Human_SNP_ID_528316648 m1A Human chr13 - 41879436 41879436 41879436 AGACAGCAGAGGATGGAAGCAGTGAAATAACCAATGATGAAAGAGAAGAAAGGTGTGTGTGTGTG AGACAGCAGAGGATGGAAGCAGTGAAATAACCGATGATGAAAGAGAAGAAAGGTGTGTGTGTGTG T C VWA8 Ensembl:ENSG00000102763 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:41879283..41879511 26863196 MeRIP-seq:(Medium) rs1278069637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23595731 RMVar_hsa_circ_59073,RMVar_hsa_circ_125325,RMVar_hsa_circ_162987,RMVar_hsa_circ_104308,RMVar_hsa_circ_94911,RMVar_hsa_circ_162990,RMVar_hsa_circ_9497,RMVar_hsa_circ_162991,RMVar_hsa_circ_16742,RMVar_hsa_circ_107996,RMVar_hsa_circ_163003,RMVar_hsa_circ_348883,RMVar_hsa_circ_365493,RMVar_hsa_circ_319906,RMVar_hsa_circ_54850,RMVar_hsa_circ_81065,RMVar_hsa_circ_163015,RMVar_hsa_circ_317709,RMVar_hsa_circ_293850,RMVar_hsa_circ_163036,RMVar_hsa_circ_26626,RMVar_hsa_circ_75357,RMVar_hsa_circ_368736,RMVar_hsa_circ_73832,RMVar_hsa_circ_316119,RMVar_hsa_circ_368743,RMVar_hsa_circ_374710,RMVar_hsa_circ_308484,RMVar_hsa_circ_163025,RMVar_hsa_circ_163026,RMVar_hsa_circ_163024,RMVar_hsa_circ_371891,RMVar_hsa_circ_329450,RMVar_hsa_circ_55717,RMVar_hsa_circ_72790,RMVar_hsa_circ_163032,RMVar_hsa_circ_114502,RMVar_hsa_circ_298256,RMVar_hsa_circ_312307,RMVar_hsa_circ_277963,RMVar_hsa_circ_271408,RMVar_hsa_circ_163038,RMVar_hsa_circ_163039,RMVar_hsa_circ_163040,RMVar_hsa_circ_163037,RMVar_hsa_circ_163041,RMVar_hsa_circ_268292,RMVar_hsa_circ_304242 92092 RMVar_ID_92092 Human_SNP_ID_528354105 m1A Human chr13 + 42040708 42040708 42040708 GGGACCGGCGCGGGGGCGGGAGAGCGCGGCGGAAGCCGGAGACGGCGGGTGGGCCGGTGGCTGGC GGGACCGGCGCGGGGGCGGGAGAGCGCGGCGGCAGCCGGAGACGGCGGGTGGGCCGGTGGCTGGC A C DGKH Ensembl:ENSG00000102780 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:42040659..42040797;chr13:42040661..42040806 26863196 MeRIP-seq:(Medium) rs923800265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9323460,Human_RBP_ID_9417300 92093 RMVar_ID_92093 Human_SNP_ID_528356149 m1A Human chr13 - 42048888 42048888 42048888 CTGGGGTCCCTCTTGCTCCGCTTCGCTGTCAGACGAATCCTCTCCCGGCCCCGCCGAGGCAGCGG CTGGGGTCCCTCTTGCTCCGCTTCGCTGTCAGTCGAATCCTCTCCCGGCCCCGCCGAGGCAGCGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:42048797..42048928 26863196 MeRIP-seq:(Medium) rs751162443 Functional Loss SNV dbSNP153 33..33 33 - - - 92094 RMVar_ID_92094 Human_SNP_ID_528368095 m1A Human chr13 - 42101684 42101684 42101684 CTCTTTCTTGCCACTGTCAGACCTCTAGAATCAATACTCCTCACCTCCATTTCTTTATCAAACAT CTCTTTCTTGCCACTGTCAGACCTCTAGAATCTATACTCCTCACCTCCATTTCTTTATCAAACAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:42101683..42101858 26863196 MeRIP-seq:(Medium) rs142643232 Functional Loss SNV dbSNP153 33..33 33 - - - 92095 RMVar_ID_92095 Human_SNP_ID_528407646 m1A Human chr13 - 42272197 42272197 42272197 CCTGGGGGCCGCAGCCTCCGCAGCTCACAGACATGTCACCGGCCTCAACGACCCGTGAGCGAGCC CCTGGGGGCCGCAGCCTCCGCAGCTCACAGACTTGTCACCGGCCTCAACGACCCGTGAGCGAGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:42272148..42272420 26863196 MeRIP-seq:(Medium) rs1441155585 Functional Loss SNV dbSNP153 33..33 33 - - - 92096 RMVar_ID_92096 Human_SNP_ID_528407647 m1A Human chr13 - 42272197 42272197 42272197 CCTGGGGGCCGCAGCCTCCGCAGCTCACAGACATGTCACCGGCCTCAACGACCCGTGAGCGAGCC CCTGGGGGCCGCAGCCTCCGCAGCTCACAGACGTGTCACCGGCCTCAACGACCCGTGAGCGAGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:42272148..42272420 26863196 MeRIP-seq:(Medium) rs1441155585 Functional Loss SNV dbSNP153 33..33 33 - - - 92097 RMVar_ID_92097 Human_SNP_ID_528599555 m1A Human chr13 - 43059820 43059820 43059820 CCCGCGAAACATTGCTCCTAACTGCACCGCCTATCCCAAAACCTGTAAGAACTAATGATAATCCA CCCGCGAAACATTGCTCCTAACTGCACCGCCTGTCCCAAAACCTGTAAGAACTAATGATAATCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:43059815..43059957 26863196 MeRIP-seq:(Medium) rs925646316 Functional Loss SNV dbSNP153 33..33 33 - - - 92098 RMVar_ID_92098 Human_SNP_ID_528599567 m1A Human chr13 + 43059841 43059840 43059842 AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCAATGTTTCGCGGGCATGGGGTGGATCTCACAAAG AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCA__GTTTCGCGGGCATGGGGTGGATCTCACAAAG AAT A DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43059838..43060029 26863196 MeRIP-seq:(Medium) rs1491142382 Functional Loss DEL dbSNP153 33..34 33 - - - 92099 RMVar_ID_92099 Human_SNP_ID_528599569 m1A Human chr13 + 43059841 43059841 43059841 AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCAATGTTTCGCGGGCATGGGGTGGATCTCACAAAG AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCACTGTTTCGCGGGCATGGGGTGGATCTCACAAAG A C DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43059838..43060029 26863196 MeRIP-seq:(Medium) rs1051993242 Functional Loss SNV dbSNP153 33..33 33 - - - 92100 RMVar_ID_92100 Human_SNP_ID_528599570 m1A Human chr13 + 43059841 43059841 43059841 AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCAATGTTTCGCGGGCATGGGGTGGATCTCACAAAG AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCAGTGTTTCGCGGGCATGGGGTGGATCTCACAAAG A G DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43059838..43060029 26863196 MeRIP-seq:(Medium) rs1051993242 Functional Loss SNV dbSNP153 33..33 33 - - - 92101 RMVar_ID_92101 Human_SNP_ID_528599571 m1A Human chr13 + 43059841 43059841 43059841 AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCAATGTTTCGCGGGCATGGGGTGGATCTCACAAAG AGGTTTTGGGATAGGCGGTGCAGTTAGGAGCATTGTTTCGCGGGCATGGGGTGGATCTCACAAAG A T DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43059838..43060029 26863196 MeRIP-seq:(Medium) rs1051993242 Functional Loss SNV dbSNP153 33..33 33 - - - 92102 RMVar_ID_92102 Human_SNP_ID_528599672 m1A Human chr13 + 43060162 43060162 43060162 CAAAACAAAATAGTGAAGTGTTGGAGCGGCGAAAAATTTTGGGGGTGGTATGGAGAGATAATGGG CAAAACAAAATAGTGAAGTGTTGGAGCGGCGACAAATTTTGGGGGTGGTATGGAGAGATAATGGG A C DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:43060155..43060275 26863196 MeRIP-seq:(Medium) rs1020899371 Functional Loss SNV dbSNP153 33..33 33 - - - 92103 RMVar_ID_92103 Human_SNP_ID_528599673 m1A Human chr13 + 43060162 43060162 43060162 CAAAACAAAATAGTGAAGTGTTGGAGCGGCGAAAAATTTTGGGGGTGGTATGGAGAGATAATGGG CAAAACAAAATAGTGAAGTGTTGGAGCGGCGATAAATTTTGGGGGTGGTATGGAGAGATAATGGG A T DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:43060155..43060275 26863196 MeRIP-seq:(Medium) rs1020899371 Functional Loss SNV dbSNP153 33..33 33 - - - 92104 RMVar_ID_92104 Human_SNP_ID_528599895 m1A Human chr13 - 43061048 43061048 43061048 GAAATCTATCCTCAAGGAAATCACTTCTCAGCATTCCATCTGCTATTCTGCTACTCCTCAGGAAT GAAATCTATCCTCAAGGAAATCACTTCTCAGCGTTCCATCTGCTATTCTGCTACTCCTCAGGAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43061047..43061209 26863196 MeRIP-seq:(Medium) rs1290752399 Functional Loss SNV dbSNP153 33..33 33 - - - 92105 RMVar_ID_92105 Human_SNP_ID_528788557 m1A Human chr13 - 43879362 43879362 43879362 CCGAGTCCGGAAAGGGTCGCGAGGAGGCAGCTAGGGGCCCCTTGAGGAGGGATAGGGCGGCGGAA CCGAGTCCGGAAAGGGTCGCGAGGAGGCAGCTTGGGGCCCCTTGAGGAGGGATAGGGCGGCGGAA T A CCDC122 Ensembl:ENSG00000151773 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:43879226..43879544 26863196 MeRIP-seq:(Medium) rs1055835385 Functional Loss SNV dbSNP153 33..33 33 - - - 92106 RMVar_ID_92106 Human_SNP_ID_528788558 m1A Human chr13 - 43879366 43879366 43879366 CAGGCCGAGTCCGGAAAGGGTCGCGAGGAGGCAGCTAGGGGCCCCTTGAGGAGGGATAGGGCGGC CAGGCCGAGTCCGGAAAGGGTCGCGAGGAGGCGGCTAGGGGCCCCTTGAGGAGGGATAGGGCGGC T C CCDC122 Ensembl:ENSG00000151773 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43879172..43879534 26863196 MeRIP-seq:(Medium) rs1342755648 Functional Loss SNV dbSNP153 33..33 33 - - - 92107 RMVar_ID_92107 Human_SNP_ID_528788893 m1A Human chr13 - 43879961 43879961 43879961 CCCGCTCTTCACCTTCGGTTGCACACCGGTCTACGGCGACCTCTGTGACAATTTGCCGCCCCGTC CCCGCTCTTCACCTTCGGTTGCACACCGGTCTGCGGCGACCTCTGTGACAATTTGCCGCCCCGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:43879881..43880082 26863196 MeRIP-seq:(Medium) rs1203852248 Functional Loss SNV dbSNP153 33..33 33 - - - 92108 RMVar_ID_92108 Human_SNP_ID_528788921 m1A Human chr13 - 43880071 43880071 43880071 GGCGCAGGCTGTGGCTCTGCACCTGCCCGGGCACCTCCACCGGCGGCTCACAGCCCATTCGGGAC GGCGCAGGCTGTGGCTCTGCACCTGCCCGGGCCCCTCCACCGGCGGCTCACAGCCCATTCGGGAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:43879931..43880082 26863196 MeRIP-seq:(Medium) rs1286102569 Functional Loss SNV dbSNP153 33..33 33 - - - 92109 RMVar_ID_92109 Human_SNP_ID_528791693 m1A Human chr13 + 43892053 43892053 43892053 TGAACCAGGGCATGAAACTGAAAGTGCATAACATATTCTAGAGAGAGAAGGGTGTGGGCATGAGT TGAACCAGGGCATGAAACTGAAAGTGCATAACGTATTCTAGAGAGAGAAGGGTGTGGGCATGAGT A G LACC1,AL512506.3 Ensembl:ENSG00000179630,Ensembl:ENSG00000281883 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:43892002..43892232 26863196 MeRIP-seq:(Medium) rs1410344528 Functional Loss SNV dbSNP153 33..33 33 - - - 92110 RMVar_ID_92110 Human_SNP_ID_528851439 m1A Human chr13 + 44146924 44146924 44146924 AGATAAATGAGCAGAGCCGTGATCAGGACCAGAGAGGAGGCAACAGAAAAGAGATGCTCAGGATA AGATAAATGAGCAGAGCCGTGATCAGGACCAGGGAGGAGGCAACAGAAAAGAGATGCTCAGGATA A G SMIM2-AS1 Ensembl:ENSG00000227258 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:44146920..44146989 26863196 MeRIP-seq:(Medium) rs1370937389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5562230 92111 RMVar_ID_92111 Human_SNP_ID_528886191 m1A Human chr13 + 44307192 44307192 44307192 AAAGAAAGGAAGAAAGGAAGAGAAAGAAAGAAAGAAAGGAAGAGAAAGAAAGACAGAAAGAAAGA AAAGAAAGGAAGAAAGGAAGAGAAAGAAAGAACGAAAGGAAGAGAAAGAAAGACAGAAAGAAAGA A C lnc-SERP2-7,lnc-SERP2-15 RNACentral:URS00008C025F,RNACentral:URS0000D5BE55 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:44307065..44307433;chr13:44307083..44307440 26863196 MeRIP-seq:(Medium) rs1477091672 Functional Loss SNV dbSNP153 33..33 33 - - - 92112 RMVar_ID_92112 Human_SNP_ID_528886196 m1A Human chr13 + 44307199 44307197 44307199 GGAAGAAAGGAAGAGAAAGAAAGAAAGAAAGGAAGAGAAAGAAAGACAGAAAGAAAGAAAGAAAG GGAAGAAAGGAAGAGAAAGAAAGAAAGAAAG__AGAGAAAGAAAGACAGAAAGAAAGAAAGAAAG GGA G lnc-SERP2-7 RNACentral:URS00008C025F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:44307132..44307309 26863196 MeRIP-seq:(Medium) rs1221082922 Functional Loss DEL dbSNP153 32..33 33 - - - 92113 RMVar_ID_92113 Human_SNP_ID_528886201 m1A Human chr13 + 44307199 44307199 44307199 GGAAGAAAGGAAGAGAAAGAAAGAAAGAAAGGAAGAGAAAGAAAGACAGAAAGAAAGAAAGAAAG GGAAGAAAGGAAGAGAAAGAAAGAAAGAAAGGGAGAGAAAGAAAGACAGAAAGAAAGAAAGAAAG A G lnc-SERP2-7 RNACentral:URS00008C025F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:44307132..44307309 26863196 MeRIP-seq:(Medium) rs375918795 Functional Loss SNV dbSNP153 33..33 33 - - - 92114 RMVar_ID_92114 Human_SNP_ID_528951340 m1A Human chr13 + 44576056 44576041 44576056 AATGTCTGCAGCGGCGGCGGCCGCGGCGGTGGACTCAGGCGGCTGGTGCATTGTGTTGGGTACCG AATGTCTGCAGCGGCGGC_______________CTCAGGCGGCTGGTGCATTGTGTTGGGTACCG CGGCCGCGGCGGTGGA C TSC22D1-AS1 Ensembl:ENSG00000278156 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:44576005..44576157 26863196 MeRIP-seq:(Medium) rs1218993716 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_8075501 92115 RMVar_ID_92115 Human_SNP_ID_528951347 m1A Human chr13 + 44576056 44576056 44576056 AATGTCTGCAGCGGCGGCGGCCGCGGCGGTGGACTCAGGCGGCTGGTGCATTGTGTTGGGTACCG AATGTCTGCAGCGGCGGCGGCCGCGGCGGTGGGCTCAGGCGGCTGGTGCATTGTGTTGGGTACCG A G TSC22D1-AS1 Ensembl:ENSG00000278156 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:44576005..44576157 26863196 MeRIP-seq:(Medium) rs756659374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8075501 92116 RMVar_ID_92116 Human_SNP_ID_528951606 m1A Human chr13 + 44576727 44576707 44576727 AGGAAACGCTGGCCGCGGCTGGGGCCGGGGCGACGCGGCTGCGAGCGGGGCGGCGGCGAGGCGCC AGGAAACGCTGGC____________________CGCGGCTGCGAGCGGGGCGGCGGCGAGGCGCC CCGCGGCTGGGGCCGGGGCGA C TSC22D1-AS1 Ensembl:ENSG00000278156 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:44576681..44576904 26863196 MeRIP-seq:(Medium) rs1232774727 Functional Loss DEL dbSNP153 14..33 33 - - - 92117 RMVar_ID_92117 Human_SNP_ID_528951659 m1A Human chr13 + 44576858 44576857 44576858 GGCCGGGGCGCGGCGGCGGCGGTGGCAGCGGGAGCCCAGGGACCGCTCCATCACTGGCAGCCATG GGCCGGGGCGCGGCGGCGGCGGTGGCAGCGGG_GCCCAGGGACCGCTCCATCACTGGCAGCCATG GA G TSC22D1-AS1 Ensembl:ENSG00000278156 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:44576807..44576955 32194978 MeRIP-seq:(Medium) rs950663293 Functional Loss DEL dbSNP153 33..33 33 - - - 92118 RMVar_ID_92118 Human_SNP_ID_528951712 m1A Human chr13 - 44577026 44577026 44577026 GGGTGAGGAAGAGCCGGCTGCGGAGGAAGAGGATAAGAGAGGGTCGCACCCTCCGCCCTAGCGCA GGGTGAGGAAGAGCCGGCTGCGGAGGAAGAGGTTAAGAGAGGGTCGCACCCTCCGCCCTAGCGCA T A TSC22D1 Ensembl:ENSG00000102804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:44576975..44577320 26863196 MeRIP-seq:(Medium) rs1225536441 Functional Loss SNV dbSNP153 33..33 33 - - - 92119 RMVar_ID_92119 Human_SNP_ID_529034753 m1A Human chr13 - 44917942 44917942 44917942 TTCCTGGTTTTCACCCAGGCGGCCCGGGTTCGACTCCCGGTGTGGGAACGCCGAAATTTTAGACT TTCCTGGTTTTCACCCAGGCGGCCCGGGTTCGGCTCCCGGTGTGGGAACGCCGAAATTTTAGACT T C tRNA-Glu-TTC-2-1 RNACentral:URS00003C9A26 tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs568303599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269561,Human_RBP_ID_276041,Human_RBP_ID_436412,Human_RBP_ID_996554,Human_RBP_ID_1128890,Human_RBP_ID_1272475,Human_RBP_ID_1359910,Human_RBP_ID_1484462,Human_RBP_ID_3430421,Human_RBP_ID_4279008,Human_RBP_ID_5174171,Human_RBP_ID_5257407,Human_RBP_ID_5417712,Human_RBP_ID_5438516,Human_RBP_ID_5462786,Human_RBP_ID_5492730,Human_RBP_ID_6285113,Human_RBP_ID_8248878,Human_RBP_ID_8392406,Human_RBP_ID_8790291,Human_RBP_ID_9281336,Human_RBP_ID_12163106,Human_RBP_ID_16994878,Human_RBP_ID_17686322,Human_RBP_ID_17838437,Human_RBP_ID_18199444,Human_RBP_ID_18206707,Human_RBP_ID_18268749,Human_RBP_ID_18435253,Human_RBP_ID_18511797,Human_RBP_ID_18640708,Human_RBP_ID_19862906,Human_RBP_ID_21920623,Human_RBP_ID_22180665,Human_RBP_ID_22421257,Human_RBP_ID_22796185,Human_RBP_ID_22916541,Human_RBP_ID_23110285,Human_RBP_ID_23111321,Human_RBP_ID_23126282,Human_RBP_ID_23270804,Human_RBP_ID_23306604,Human_RBP_ID_23596733,Human_RBP_ID_24530353,Human_RBP_ID_26425533,Human_RBP_ID_26619647,Human_RBP_ID_26748332,Human_RBP_ID_26916271,Human_RBP_ID_27155181,Human_RBP_ID_27223433,Human_RBP_ID_27427973,Human_RBP_ID_27558565 92120 RMVar_ID_92120 Human_SNP_ID_529051385 m1A Human chr13 - 44989313 44989313 44989313 CCCCGCCGCGGGACAGCTGGATGTTCTGGGCAATGCTGCCGCCACCGCCACCACCACTTACGTCC CCCCGCCGCGGGACAGCTGGATGTTCTGGGCAGTGCTGCCGCCACCGCCACCACCACTTACGTCC T C AL359706.1,NUFIP1 Ensembl:ENSG00000223732,Ensembl:ENSG00000083635 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:44989186..44989439 26863196 MeRIP-seq:(Medium) rs879017648 Functional Loss SNV dbSNP153 33..33 33 - - - 92121 RMVar_ID_92121 Human_SNP_ID_529051406 m1A Human chr13 - 44989351 44989351 44989351 CGAGCTGACTCCCACGTTAGGGCCCCTGAGCGACACTGCCCCGCCGCGGGACAGCTGGATGTTCT CGAGCTGACTCCCACGTTAGGGCCCCTGAGCGGCACTGCCCCGCCGCGGGACAGCTGGATGTTCT T C AL359706.1,NUFIP1 Ensembl:ENSG00000223732,Ensembl:ENSG00000083635 lincRNA,Protein coding intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:44989302..44989433 26863196 MeRIP-seq:(Medium) rs748429578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276610,Human_RBP_ID_5561456 Human_miRNA_ID_1019774,Human_miRNA_ID_1297585 92122 RMVar_ID_92122 Human_SNP_ID_529051454 m1A Human chr13 + 44989422 44989422 44989422 GCATGCCACCCGATAGGAGTCTCGAAATCACTAGTCGGCTCAGCCATACCACTGGCGGGTCCGGA GCATGCCACCCGATAGGAGTCTCGAAATCACTGGTCGGCTCAGCCATACCACTGGCGGGTCCGGA A G lnc-GPALPP1-5 RNACentral:URS00008B5DA4 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:44989332..44989433 26863410 MeRIP-seq:(Medium) rs1328537010 Functional Loss SNV dbSNP153 33..33 33 - - - 92123 RMVar_ID_92123 Human_SNP_ID_365356474 m1A Human chr8 - 60517140 60517140 60517140 TCCTCCCGCTGCTGCTCCTCCTCCGCGCCCCAACCCCGGTGCCGCTCAGCCTCGAAACGCCAGGC TCCTCCCGCTGCTGCTCCTCCTCCGCGCCCCACCCCCGGTGCCGCTCAGCCTCGAAACGCCAGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:60516951..60517250 26863196 MeRIP-seq:(Medium) rs972144104 Functional Loss SNV dbSNP153 33..33 33 - - - 92124 RMVar_ID_92124 Human_SNP_ID_365367851 m1A Human chr8 - 60558859 60558859 60558859 TTGTCTGTAAACTGTAGCAATAAGCATGATTTACCAACACCTGAAAGTTAAAAAAAAATAAATAA TTGTCTGTAAACTGTAGCAATAAGCATGATTTCCCAACACCTGAAAGTTAAAAAAAAATAAATAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:60558851..60558875 26863196 MeRIP-seq:(Medium) rs1429324364 Functional Loss SNV dbSNP153 33..33 33 - - - 92125 RMVar_ID_92125 Human_SNP_ID_365383773 m1A Human chr8 + 60621869 60621868 60621869 GAAGGGGATATGACAATAAATCTATCAGATGGAAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA GAAGGGGATATGACAATAAATCTATCAGATGG_AAATCCTGTTACAAAGTAGAAAAGCTTTAGTA GA G RAB2A Ensembl:ENSG00000104388 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1419737063 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_702173,Human_RBP_ID_3163413,Human_RBP_ID_26559228 92126 RMVar_ID_92126 Human_SNP_ID_365383774 m1A Human chr8 + 60621869 60621869 60621869 GAAGGGGATATGACAATAAATCTATCAGATGGAAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA GAAGGGGATATGACAATAAATCTATCAGATGGGAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA A G RAB2A Ensembl:ENSG00000104388 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_702173,Human_RBP_ID_3163413,Human_RBP_ID_26559228 GWAS_ID_11997,GWAS_ID_11998,GWAS_ID_11999,GWAS_ID_12000,GWAS_ID_12001,GWAS_ID_12002,GWAS_ID_12003,GWAS_ID_12004,GWAS_ID_12005,GWAS_ID_12006,GWAS_ID_12007,GWAS_ID_12008,GWAS_ID_12009,GWAS_ID_12010,GWAS_ID_12011,GWAS_ID_12012,GWAS_ID_12013,GWAS_ID_12014,GWAS_ID_12015,GWAS_ID_12016,GWAS_ID_12017,GWAS_ID_12018,GWAS_ID_12019,GWAS_ID_12020,GWAS_ID_12021,GWAS_ID_12022,GWAS_ID_12023,GWAS_ID_12024,GWAS_ID_12025,GWAS_ID_12026,GWAS_ID_12027,GWAS_ID_12028,GWAS_ID_12029,GWAS_ID_12030,GWAS_ID_12031,GWAS_ID_12032,GWAS_ID_12033,GWAS_ID_12034,GWAS_ID_12035,GWAS_ID_12036,GWAS_ID_12037,GWAS_ID_12038,GWAS_ID_12039,GWAS_ID_12040,GWAS_ID_12041,GWAS_ID_12042,GWAS_ID_12043,GWAS_ID_12044,GWAS_ID_12045,GWAS_ID_12046,GWAS_ID_12047,GWAS_ID_12048,GWAS_ID_12049,GWAS_ID_12050,GWAS_ID_12051,GWAS_ID_12052,GWAS_ID_12053,GWAS_ID_12054,GWAS_ID_12055,GWAS_ID_12056,GWAS_ID_12057,GWAS_ID_12058,GWAS_ID_12059 92127 RMVar_ID_92127 Human_SNP_ID_365383775 m1A Human chr8 + 60621869 60621869 60621869 GAAGGGGATATGACAATAAATCTATCAGATGGAAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA GAAGGGGATATGACAATAAATCTATCAGATGGTAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA A T RAB2A Ensembl:ENSG00000104388 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_702173,Human_RBP_ID_3163413,Human_RBP_ID_26559228 GWAS_ID_11997,GWAS_ID_11998,GWAS_ID_11999,GWAS_ID_12000,GWAS_ID_12001,GWAS_ID_12002,GWAS_ID_12003,GWAS_ID_12004,GWAS_ID_12005,GWAS_ID_12006,GWAS_ID_12007,GWAS_ID_12008,GWAS_ID_12009,GWAS_ID_12010,GWAS_ID_12011,GWAS_ID_12012,GWAS_ID_12013,GWAS_ID_12014,GWAS_ID_12015,GWAS_ID_12016,GWAS_ID_12017,GWAS_ID_12018,GWAS_ID_12019,GWAS_ID_12020,GWAS_ID_12021,GWAS_ID_12022,GWAS_ID_12023,GWAS_ID_12024,GWAS_ID_12025,GWAS_ID_12026,GWAS_ID_12027,GWAS_ID_12028,GWAS_ID_12029,GWAS_ID_12030,GWAS_ID_12031,GWAS_ID_12032,GWAS_ID_12033,GWAS_ID_12034,GWAS_ID_12035,GWAS_ID_12036,GWAS_ID_12037,GWAS_ID_12038,GWAS_ID_12039,GWAS_ID_12040,GWAS_ID_12041,GWAS_ID_12042,GWAS_ID_12043,GWAS_ID_12044,GWAS_ID_12045,GWAS_ID_12046,GWAS_ID_12047,GWAS_ID_12048,GWAS_ID_12049,GWAS_ID_12050,GWAS_ID_12051,GWAS_ID_12052,GWAS_ID_12053,GWAS_ID_12054,GWAS_ID_12055,GWAS_ID_12056,GWAS_ID_12057,GWAS_ID_12058,GWAS_ID_12059 92128 RMVar_ID_92128 Human_SNP_ID_365398200 m1A Human chr8 - 60678833 60678833 60678833 ATCCGATAGTTCCCGAGCACGAGCGCGTCCGCACCACCACGACTCAACCCCCGCGCCGCCGCCGC ATCCGATAGTTCCCGAGCACGAGCGCGTCCGCCCCACCACGACTCAACCCCCGCGCCGCCGCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:60678786..60679352 26863196 MeRIP-seq:(Medium) rs1293104473 Functional Loss SNV dbSNP153 33..33 33 - - - 92129 RMVar_ID_92129 Human_SNP_ID_365398375 m1A Human chr8 - 60679287 60679261 60679287 TCGGGGCGCGGGTTCGGGCCCCGCGGGCGGCGACGCCGGCGACACTACGCGGGCGGCGCTGCGCT TCGGGGCGCGGGTTCGGGCCCCGCGGGCGGCG__________________________CTGCGCT GCGCCGCCCGCGTAGTGTCGCCGGCGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:60679276..60679377 26863196 MeRIP-seq:(Medium) rs971060068 Functional Loss DEL dbSNP153 33..58 33 - - - 92130 RMVar_ID_92130 Human_SNP_ID_365398533 m1A Human chr8 - 60679537 60679537 60679537 GCCCAACTTTTCCTCCTTCCTTTTTCTCTCGAATGGAGCCGGCAACTCGTGCTCGGCGCCGGCGG GCCCAACTTTTCCTCCTTCCTTTTTCTCTCGAGTGGAGCCGGCAACTCGTGCTCGGCGCCGGCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:60679528..60679599 26863196 MeRIP-seq:(Medium) rs1209835707 Functional Loss SNV dbSNP153 33..33 33 - - - 92131 RMVar_ID_92131 Human_SNP_ID_365398653 m1A Human chr8 + 60679809 60679808 60679809 CCGCCACCGAGCGAGGTGGGTCGGCGGCGGGGAAAGTGCGCGGGGCGCCGCGTGGGGCGGGGGCA CCGCCACCGAGCGAGGTGGGTCGGCGGCGGGG_AAGTGCGCGGGGCGCCGCGTGGGGCGGGGGCA GA G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:60679806..60679910 26863196 MeRIP-seq:(Medium) rs562403018 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3885798,Human_RBP_ID_8221085 92132 RMVar_ID_92132 Human_SNP_ID_365398654 m1A Human chr8 + 60679809 60679809 60679809 CCGCCACCGAGCGAGGTGGGTCGGCGGCGGGGAAAGTGCGCGGGGCGCCGCGTGGGGCGGGGGCA CCGCCACCGAGCGAGGTGGGTCGGCGGCGGGGGAAGTGCGCGGGGCGCCGCGTGGGGCGGGGGCA A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:60679806..60679910 26863196 MeRIP-seq:(Medium) rs1361905011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885798,Human_RBP_ID_8221085 92133 RMVar_ID_92133 Human_SNP_ID_365398898 m1A Human chr8 - 60680395 60680394 60680396 CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGCGACCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGC__CCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC GTC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:60680303..60680431 26863196 MeRIP-seq:(Medium) rs1245143744 Functional Loss DEL dbSNP153 32..33 33 - - - 92134 RMVar_ID_92134 Human_SNP_ID_365398899 m1A Human chr8 - 60680395 60680395 60680395 CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGCGACCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGCGGCCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:60680303..60680431 26863196 MeRIP-seq:(Medium) rs969442449 Functional Loss SNV dbSNP153 33..33 33 - - - 92135 RMVar_ID_92135 Human_SNP_ID_365398900 m1A Human chr8 - 60680395 60680395 60680395 CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGCGACCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC CGCCGCCGCCGCCCCCGCCCCCCCCCCCCGCGCCCTCGACAGCCCCGCGCCGCCGCGCCCGCCCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:60680303..60680431 26863196 MeRIP-seq:(Medium) rs969442449 Functional Loss SNV dbSNP153 33..33 33 - - - 92136 RMVar_ID_92136 Human_SNP_ID_365407152 m1A Human chr8 - 60714312 60714312 60714312 CGCAGCTCCGGCCCCGAGCCACTGAGGCGGGCATGAGGTGAAGCGAGCGCCCCGAGTGGGTGGGA CGCAGCTCCGGCCCCGAGCCACTGAGGCGGGCGTGAGGTGAAGCGAGCGCCCCGAGTGGGTGGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:60714310..60714441 26863196 MeRIP-seq:(Medium) rs1409330830 Functional Loss SNV dbSNP153 33..33 33 - - - 92137 RMVar_ID_92137 Human_SNP_ID_365412129 m1A Human chr8 + 60734534 60734534 60734534 TCAGCCTGAAGAGGGAGGGTTGAGGGTCAGGAAGCTTCCGAAGATGGGTGATAACAAAGGAACTG TCAGCCTGAAGAGGGAGGGTTGAGGGTCAGGAGGCTTCCGAAGATGGGTGATAACAAAGGAACTG A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:60734529..60734761 26863196 MeRIP-seq:(Medium) rs76066600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3163630,Human_RBP_ID_7846900 92138 RMVar_ID_92138 Human_SNP_ID_365412132 m1A Human chr8 + 60734543 60734543 60734543 AGAGGGAGGGTTGAGGGTCAGGAAGCTTCCGAAGATGGGTGATAACAAAGGAACTGAGATGAAAA AGAGGGAGGGTTGAGGGTCAGGAAGCTTCCGAGGATGGGTGATAACAAAGGAACTGAGATGAAAA A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:60734535..60734651 26863196 MeRIP-seq:(Medium) rs150025193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3163630 92139 RMVar_ID_92139 Human_SNP_ID_365438978 m1A Human chr8 + 60843840 60843840 60843840 TTGGGTAGGGAAGGGAAGTGAGGTACCGGCAGATAGAGCAGTGTGTTCCAAGGCCTAGCAGTGAG TTGGGTAGGGAAGGGAAGTGAGGTACCGGCAGGTAGAGCAGTGTGTTCCAAGGCCTAGCAGTGAG A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:60843833..60843944 26863196 MeRIP-seq:(Medium) rs759285772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76107,RMVar_hsa_circ_79266,RMVar_hsa_circ_252260,RMVar_hsa_circ_63165,RMVar_hsa_circ_252259,RMVar_hsa_circ_268589,RMVar_hsa_circ_13184,RMVar_hsa_circ_359239,RMVar_hsa_circ_269627,RMVar_hsa_circ_73304,RMVar_hsa_circ_267861,RMVar_hsa_circ_107755,RMVar_hsa_circ_75257,RMVar_hsa_circ_252283,RMVar_hsa_circ_34287 92140 RMVar_ID_92140 Human_SNP_ID_365440836 m1A Human chr8 - 60850981 60850981 60850981 AAAATTATTTGAATCATACTGATAAGCAAAAGAAGGAAGGGGGGTGGGTAGGAAAGAGTAATAAT AAAATTATTTGAATCATACTGATAAGCAAAAGGAGGAAGGGGGGTGGGTAGGAAAGAGTAATAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:60850978..60851071 26863196 MeRIP-seq:(Medium) rs1294663861 Functional Loss SNV dbSNP153 33..33 33 - - - 92141 RMVar_ID_92141 Human_SNP_ID_365620027 m1A Human chr8 - 61576820 61576820 61576820 ATTGAGGAAGCAGTGAATGCATTTAAAGAACTAGTACGCAAATACCCTCAGAGTCCACGAGCAAG ATTGAGGAAGCAGTGAATGCATTTAAAGAACTGGTACGCAAATACCCTCAGAGTCCACGAGCAAG T C ASPH Ensembl:ENSG00000198363 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:61576719..61576820 26863196 MeRIP-seq:(Medium) rs1363006694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89319,Human_RBP_ID_3164186,Human_RBP_ID_9405520 Human_Splice_Rec_980832,Human_Splice_Rec_980833,Human_Splice_Rec_980878,Human_Splice_Rec_980879,Human_Splice_Rec_980918,Human_Splice_Rec_980919,Human_Splice_Rec_980928,Human_Splice_Rec_980934 RMVar_hsa_circ_13547,RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_356125,RMVar_hsa_circ_126733,RMVar_hsa_circ_61508,RMVar_hsa_circ_62714,RMVar_hsa_circ_252302,RMVar_hsa_circ_357580,RMVar_hsa_circ_354051,RMVar_hsa_circ_59143,RMVar_hsa_circ_351342,RMVar_hsa_circ_356752,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_353568,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_252306,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_74702,RMVar_hsa_circ_360147,RMVar_hsa_circ_362743,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_355039,RMVar_hsa_circ_362181,RMVar_hsa_circ_350762,RMVar_hsa_circ_59281,RMVar_hsa_circ_317219,RMVar_hsa_circ_336392,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_376937,RMVar_hsa_circ_344297,RMVar_hsa_circ_324201,RMVar_hsa_circ_252311,RMVar_hsa_circ_252312,RMVar_hsa_circ_252310 92142 RMVar_ID_92142 Human_SNP_ID_365622493 m1A Human chr8 - 61586071 61586071 61586071 TCTAGGAAGGAGGAGGGCATCAACTGTGTCAAATGTTGCAAAAGGGCCAGGTAAAATAGGAAGAA TCTAGGAAGGAGGAGGGCATCAACTGTGTCAAGTGTTGCAAAAGGGCCAGGTAAAATAGGAAGAA T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61586069..61586142 26863196 MeRIP-seq:(Medium) rs1293549474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13547,RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_126733,RMVar_hsa_circ_61508,RMVar_hsa_circ_62714,RMVar_hsa_circ_252302,RMVar_hsa_circ_357580,RMVar_hsa_circ_59143,RMVar_hsa_circ_356752,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_362743,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_355039,RMVar_hsa_circ_362181,RMVar_hsa_circ_350762,RMVar_hsa_circ_70818,RMVar_hsa_circ_317219,RMVar_hsa_circ_336392,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_376937,RMVar_hsa_circ_324201,RMVar_hsa_circ_252311,RMVar_hsa_circ_252312,RMVar_hsa_circ_356313,RMVar_hsa_circ_37564 92143 RMVar_ID_92143 Human_SNP_ID_365634128 m1A Human chr8 + 61637564 61637564 61637564 ACCAAAAAAAAAAAAATTTGTTTTGTTTTCCCAGGTGAGTCATGACATAAAGACCCATCTTTCAA ACCAAAAAAAAAAAAATTTGTTTTGTTTTCCCCGGTGAGTCATGACATAAAGACCCATCTTTCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61637562..61637679 26863196 MeRIP-seq:(Medium) rs1309740495 Functional Loss SNV dbSNP153 33..33 33 - - - 92144 RMVar_ID_92144 Human_SNP_ID_365634563 m1A Human chr8 - 61639254 61639252 61639254 GAAGAAATTAGATTGTTCAATGGAAGAAAGAGAGGGTGACGAGAAGCAAGCTTAAGAAAGAGTGG GAAGAAATTAGATTGTTCAATGGAAGAAAGAG__GGTGACGAGAAGCAAGCTTAAGAAAGAGTGG CCT C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61639251..61639570 26863196 MeRIP-seq:(Medium) rs1333095242 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_13547,RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252302,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_362181,RMVar_hsa_circ_32262,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_376937,RMVar_hsa_circ_324201,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_349562,RMVar_hsa_circ_359967,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_291764,RMVar_hsa_circ_252314,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_252313,RMVar_hsa_circ_362475,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_306904,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_377230,RMVar_hsa_circ_309039,RMVar_hsa_circ_61421,RMVar_hsa_circ_252320 92145 RMVar_ID_92145 Human_SNP_ID_365634707 m1A Human chr8 - 61639868 61639866 61639868 CATACACTCTTCTGCTTCTGCAGCCTGGTGACAGGGGGTGCTCTTTTCCTAACGTGGGAGAGACT CATACACTCTTCTGCTTCTGCAGCCTGGTGAC__GGGGTGCTCTTTTCCTAACGTGGGAGAGACT CCT C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61639866..61640034 26863196 MeRIP-seq:(Medium) rs1337716042 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_13547,RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252302,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_362181,RMVar_hsa_circ_32262,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_376937,RMVar_hsa_circ_324201,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_349562,RMVar_hsa_circ_359967,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_291764,RMVar_hsa_circ_252314,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_252313,RMVar_hsa_circ_362475,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_306904,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_377230,RMVar_hsa_circ_309039,RMVar_hsa_circ_61421,RMVar_hsa_circ_252320 92146 RMVar_ID_92146 Human_SNP_ID_365634709 m1A Human chr8 - 61639868 61639868 61639868 CATACACTCTTCTGCTTCTGCAGCCTGGTGACAGGGGGTGCTCTTTTCCTAACGTGGGAGAGACT CATACACTCTTCTGCTTCTGCAGCCTGGTGACTGGGGGTGCTCTTTTCCTAACGTGGGAGAGACT T A ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61639866..61640034 26863196 MeRIP-seq:(Medium) rs1027856906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13547,RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252302,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_362181,RMVar_hsa_circ_32262,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_376937,RMVar_hsa_circ_324201,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_349562,RMVar_hsa_circ_359967,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_291764,RMVar_hsa_circ_252314,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_252313,RMVar_hsa_circ_362475,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_306904,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_377230,RMVar_hsa_circ_309039,RMVar_hsa_circ_61421,RMVar_hsa_circ_252320 92147 RMVar_ID_92147 Human_SNP_ID_365637049 m1A Human chr8 - 61649688 61649687 61649688 TGCCTCAGCCAAAGGAGGGGATGGAGAGAAATAGAAAGAACCCTAAGATGTTTAGGTGGTGGGGG TGCCTCAGCCAAAGGAGGGGATGGAGAGAAAT_GAAAGAACCCTAAGATGTTTAGGTGGTGGGGG CT C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61649685..61649765 26863196 MeRIP-seq:(Medium) rs1370898068 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_67952,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_354845,RMVar_hsa_circ_362181,RMVar_hsa_circ_46334,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_359967,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_309039,RMVar_hsa_circ_61421,RMVar_hsa_circ_252320,RMVar_hsa_circ_252322,RMVar_hsa_circ_371589,RMVar_hsa_circ_373031,RMVar_hsa_circ_252323,RMVar_hsa_circ_75674,RMVar_hsa_circ_39855,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_47583,RMVar_hsa_circ_14252,RMVar_hsa_circ_252327,RMVar_hsa_circ_302003 92148 RMVar_ID_92148 Human_SNP_ID_365637435 m1A Human chr8 - 61651126 61651126 61651126 TTTTCTACTTAGCTATGTTTTGCAATTATTTTAGAACCCCAGAATATCGAAGATGAAGCAAAAGA TTTTCTACTTAGCTATGTTTTGCAATTATTTTGGAACCCCAGAATATCGAAGATGAAGCAAAAGA T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:61651076..61651125 26863196 MeRIP-seq:(Medium) rs898835958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89349,Human_RBP_ID_702379,Human_RBP_ID_960747,Human_RBP_ID_3164580,Human_RBP_ID_9406340,Human_RBP_ID_16449439,Human_RBP_ID_19022936,Human_RBP_ID_24549561,Human_RBP_ID_26177874 Human_Splice_Rec_980811,Human_Splice_Rec_980857,Human_Splice_Rec_980901,Human_Splice_Rec_980951,Human_Splice_Rec_980989,Human_Splice_Rec_981013,Human_Splice_Rec_981037,Human_Splice_Rec_981061,Human_Splice_Rec_981085,Human_Splice_Rec_981111,Human_Splice_Rec_981141,Human_Splice_Rec_981181,Human_Splice_Rec_981191 RMVar_hsa_circ_67952,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_354845,RMVar_hsa_circ_362181,RMVar_hsa_circ_46334,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_309039,RMVar_hsa_circ_252320,RMVar_hsa_circ_252322,RMVar_hsa_circ_371589,RMVar_hsa_circ_373031,RMVar_hsa_circ_252323,RMVar_hsa_circ_75674,RMVar_hsa_circ_93208,RMVar_hsa_circ_39855,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_47583,RMVar_hsa_circ_14252,RMVar_hsa_circ_252327,RMVar_hsa_circ_302003,RMVar_hsa_circ_348386,RMVar_hsa_circ_351145,RMVar_hsa_circ_272199,RMVar_hsa_circ_252328,RMVar_hsa_circ_252329 92149 RMVar_ID_92149 Human_SNP_ID_365638008 m1A Human chr8 - 61653553 61653553 61653553 AGGTTCCTGTGGAGGCAGGTAAGCTTGTCCTCATCCTCGAGTCTCGCCCAGGTGTGCCAGAGCCT AGGTTCCTGTGGAGGCAGGTAAGCTTGTCCTCGTCCTCGAGTCTCGCCCAGGTGTGCCAGAGCCT T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:61653551..61653675 26863196 MeRIP-seq:(Medium) rs535998067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959176 RMVar_hsa_circ_67952,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_354845,RMVar_hsa_circ_362181,RMVar_hsa_circ_46334,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_309039,RMVar_hsa_circ_252320,RMVar_hsa_circ_252322,RMVar_hsa_circ_371589,RMVar_hsa_circ_373031,RMVar_hsa_circ_252323,RMVar_hsa_circ_75674,RMVar_hsa_circ_93208,RMVar_hsa_circ_39855,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_47583,RMVar_hsa_circ_14252,RMVar_hsa_circ_252327,RMVar_hsa_circ_302003,RMVar_hsa_circ_348386,RMVar_hsa_circ_351145,RMVar_hsa_circ_272199,RMVar_hsa_circ_252328,RMVar_hsa_circ_252329 92150 RMVar_ID_92150 Human_SNP_ID_365645110 m1A Human chr8 - 61684186 61684185 61684187 TTATGATATCTTACATTTATTTCTAAACAGAGACAAAGCATGGAGGACACAAGAATGGGAGGAAA TTATGATATCTTACATTTATTTCTAAACAGA__CAAAGCATGGAGGACACAAGAATGGGAGGAAA GTC G ASPH Ensembl:ENSG00000198363 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:61683999..61684243 26863196 MeRIP-seq:(Medium) rs762634513 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9405532 Human_Splice_Rec_980806,Human_Splice_Rec_980852,Human_Splice_Rec_980930,Human_Splice_Rec_980984,Human_Splice_Rec_981008,Human_Splice_Rec_981030,Human_Splice_Rec_981056,Human_Splice_Rec_981078,Human_Splice_Rec_981104,Human_Splice_Rec_981134,Human_Splice_Rec_981176,Human_Splice_Rec_981196,Human_Splice_Rec_981200,Human_Splice_Rec_981204,Human_Splice_Rec_981212,Human_Splice_Rec_981218,Human_Splice_Rec_981224,Human_Splice_Rec_981232 Human_miRNA_ID_2896518,Human_miRNA_ID_2896519,Human_miRNA_ID_2896520,Human_miRNA_ID_2896521 RMVar_hsa_circ_372416,RMVar_hsa_circ_252305,RMVar_hsa_circ_354845,RMVar_hsa_circ_366161,RMVar_hsa_circ_252316,RMVar_hsa_circ_37564,RMVar_hsa_circ_322811,RMVar_hsa_circ_326261,RMVar_hsa_circ_252317,RMVar_hsa_circ_309039,RMVar_hsa_circ_252320,RMVar_hsa_circ_371589,RMVar_hsa_circ_252323,RMVar_hsa_circ_75674,RMVar_hsa_circ_93208,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_272199,RMVar_hsa_circ_17017,RMVar_hsa_circ_252328,RMVar_hsa_circ_252329,RMVar_hsa_circ_106376,RMVar_hsa_circ_252330,RMVar_hsa_circ_42874,RMVar_hsa_circ_271012,RMVar_hsa_circ_252331,RMVar_hsa_circ_378272,RMVar_hsa_circ_252332,RMVar_hsa_circ_252333,RMVar_hsa_circ_343188 92151 RMVar_ID_92151 Human_SNP_ID_365647052 m1A Human chr8 - 61693006 61693006 61693006 GTTGGATAATTAGATGTCATAGACCACAGAGGAGCAGGGAGCAGGGTTTTGTTGTTGATGTCATC GTTGGATAATTAGATGTCATAGACCACAGAGGTGCAGGGAGCAGGGTTTTGTTGTTGATGTCATC T A ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:61693003..61693250 26863196 MeRIP-seq:(Medium) rs772269072 Functional Loss SNV dbSNP153 33..33 33 - - - 92152 RMVar_ID_92152 Human_SNP_ID_365647235 m1A Human chr8 - 61693748 61693748 61693748 AGGTGAAGAGGGGATATGCAGGAAGCAGAAATAAGAGAACTACAGGATCCAAGAAGAAAATGTTG AGGTGAAGAGGGGATATGCAGGAAGCAGAAATGAGAGAACTACAGGATCCAAGAAGAAAATGTTG T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:61693746..61693870 26863196 MeRIP-seq:(Medium) rs928448140 Functional Loss SNV dbSNP153 33..33 33 - - - 92153 RMVar_ID_92153 Human_SNP_ID_365647308 m1A Human chr8 + 61694022 61694022 61694022 CCAGCCTCAGCTGGGCCTCGGTGCTGCCTGCCACCCTCCCATATTCTCTACAAACTCACCTTGCC CCAGCCTCAGCTGGGCCTCGGTGCTGCCTGCCGCCCTCCCATATTCTCTACAAACTCACCTTGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:61694019..61694686 26863196 MeRIP-seq:(Medium) rs958566552 Functional Loss SNV dbSNP153 33..33 33 - - - 92154 RMVar_ID_92154 Human_SNP_ID_365652252 m1A Human chr8 - 61714326 61714326 61714326 AGAATGCCAAGAGCAGCGGCAACAGCAGCAGCAGCGGCTCCGGCAGCGGTAGCACGAGTGCGGGC AGAATGCCAAGAGCAGCGGCAACAGCAGCAGCCGCGGCTCCGGCAGCGGTAGCACGAGTGCGGGC T G ASPH Ensembl:ENSG00000198363 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:61714251..61714325 26863196 MeRIP-seq:(Medium) rs755173683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90019,Human_RBP_ID_5002181,Human_RBP_ID_5224741,Human_RBP_ID_26359149,Human_RBP_ID_27831924 Human_Splice_Rec_980805,Human_Splice_Rec_980983,Human_Splice_Rec_981007,Human_Splice_Rec_981029,Human_Splice_Rec_981055,Human_Splice_Rec_981195,Human_Splice_Rec_981217 92155 RMVar_ID_92155 Human_SNP_ID_365652297 m1A Human chr8 - 61714412 61714411 61714412 TCCCGCGTCGCGTGTGTACCCCCGCGCACTGAAGGAGGTCCGCCAGCCCTCACCAGCCCCCGCGG TCCCGCGTCGCGTGTGTACCCCCGCGCACTGA_GGAGGTCCGCCAGCCCTCACCAGCCCCCGCGG CT C ASPH Ensembl:ENSG00000198363 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:61714214..61714634 26863196 MeRIP-seq:(Medium) rs1563690185 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_90019,Human_RBP_ID_4995067,Human_RBP_ID_9405533,Human_RBP_ID_18426837,Human_RBP_ID_22410884,Human_RBP_ID_24520924,Human_RBP_ID_26359149,Human_RBP_ID_27831924 92156 RMVar_ID_92156 Human_SNP_ID_365652298 m1A Human chr8 - 61714412 61714412 61714412 TCCCGCGTCGCGTGTGTACCCCCGCGCACTGAAGGAGGTCCGCCAGCCCTCACCAGCCCCCGCGG TCCCGCGTCGCGTGTGTACCCCCGCGCACTGAGGGAGGTCCGCCAGCCCTCACCAGCCCCCGCGG T C ASPH Ensembl:ENSG00000198363 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:61714214..61714634 26863196 MeRIP-seq:(Medium) rs1482774008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90019,Human_RBP_ID_4995067,Human_RBP_ID_9405533,Human_RBP_ID_18426837,Human_RBP_ID_22410884,Human_RBP_ID_24520924,Human_RBP_ID_26359149,Human_RBP_ID_27831924 92157 RMVar_ID_92157 Human_SNP_ID_365766725 m1A Human chr8 - 62164770 62164770 62164770 CGATCCCCCAACACCACACTGAGTCTATTTCCAGGCAGCCAGTGACCAGGGGTGAGGACTTGCCC CGATCCCCCAACACCACACTGAGTCTATTTCCGGGCAGCCAGTGACCAGGGGTGAGGACTTGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:62164721..62164786 26863196 MeRIP-seq:(Medium) rs1408348894 Functional Loss SNV dbSNP153 33..33 33 - - - 92158 RMVar_ID_92158 Human_SNP_ID_365788879 m1A Human chr8 - 62248600 62248600 62248600 AGTGCCGCTGGGGAGGATCGGCCTGTCTAGTTAAGAGTCTTTGGGGAGAAAGGAAGAGGGACAGA AGTGCCGCTGGGGAGGATCGGCCTGTCTAGTTGAGAGTCTTTGGGGAGAAAGGAAGAGGGACAGA T C AC023095.1 Ensembl:ENSG00000285971 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:62248553..62248839 26863196 MeRIP-seq:(Medium) rs1282631504 Functional Loss SNV dbSNP153 33..33 33 - - - 92159 RMVar_ID_92159 Human_SNP_ID_365983973 m1A Human chr8 + 63038723 63038723 63038723 GGGTCTAGACAGCTCGAGGCTCGCCGCCCCGCAGAGTAGCAGGCCCAGCACGCACAGCAGGCAGC GGGTCTAGACAGCTCGAGGCTCGCCGCCCCGCCGAGTAGCAGGCCCAGCACGCACAGCAGGCAGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:63035735..63038800 26863410 MeRIP-seq:(Medium) rs767324259 Functional Loss SNV dbSNP153 33..33 33 - - - 92160 RMVar_ID_92160 Human_SNP_ID_365983995 m1A Human chr8 + 63038753 63038753 63038753 GCAGAGTAGCAGGCCCAGCACGCACAGCAGGCAGCCCGGACTGGCCATGGCGCTCGCCGCCTCCC GCAGAGTAGCAGGCCCAGCACGCACAGCAGGCGGCCCGGACTGGCCATGGCGCTCGCCGCCTCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:63038706..63038781;chr8:63038702..63038825 26863196 MeRIP-seq:(Medium) rs1800909 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_12060,GWAS_ID_12061,GWAS_ID_12062,GWAS_ID_12063,GWAS_ID_12064,GWAS_ID_12065,GWAS_ID_12066,GWAS_ID_12067,GWAS_ID_12068 92161 RMVar_ID_92161 Human_SNP_ID_365984010 m1A Human chr8 + 63038767 63038767 63038767 CCAGCACGCACAGCAGGCAGCCCGGACTGGCCATGGCGCTCGCCGCCTCCCGCCGCCTTTCAAAA CCAGCACGCACAGCAGGCAGCCCGGACTGGCCCTGGCGCTCGCCGCCTCCCGCCGCCTTTCAAAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:63038651..63038825 26863196 MeRIP-seq:(Medium) rs752518189 Functional Loss SNV dbSNP153 33..33 33 - - - 92162 RMVar_ID_92162 Human_SNP_ID_365984011 m1A Human chr8 + 63038767 63038767 63038767 CCAGCACGCACAGCAGGCAGCCCGGACTGGCCATGGCGCTCGCCGCCTCCCGCCGCCTTTCAAAA CCAGCACGCACAGCAGGCAGCCCGGACTGGCCGTGGCGCTCGCCGCCTCCCGCCGCCTTTCAAAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:63038651..63038825 26863196 MeRIP-seq:(Medium) rs752518189 Functional Loss SNV dbSNP153 33..33 33 - - - 92163 RMVar_ID_92163 Human_SNP_ID_366017348 m1A Human chr8 + 63168725 63168725 63168725 CGGAAAAGACGGGCCTCTTCCTCCGACTCCCGAGCGCGAGGCCCTCATTTTGGGTTCTCAGCGAA CGGAAAAGACGGGCCTCTTCCTCCGACTCCCGGGCGCGAGGCCCTCATTTTGGGTTCTCAGCGAA A G YTHDF3 Ensembl:ENSG00000185728 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:63168674..63168925 26863196 MeRIP-seq:(Medium) rs955219228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958175,Human_RBP_ID_4995070,Human_RBP_ID_18426703,Human_RBP_ID_22465868,Human_RBP_ID_23088048,Human_RBP_ID_23216311,Human_RBP_ID_24549502,Human_RBP_ID_26359152,Human_RBP_ID_27831354 RMVar_hsa_circ_124231,RMVar_hsa_circ_252352 92164 RMVar_ID_92164 Human_SNP_ID_366017527 m1A Human chr8 + 63169115 63169115 63169115 GGGCGGGCGCGGTGCCGCGGCGGGTGGGGGCAAGGACCGGTCTTAGGGGCCTTAGGACAGATCCT GGGCGGGCGCGGTGCCGCGGCGGGTGGGGGCAGGGACCGGTCTTAGGGGCCTTAGGACAGATCCT A G YTHDF3 Ensembl:ENSG00000185728 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:63169111..63169249 26863196 MeRIP-seq:(Medium) rs961277958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267962,Human_RBP_ID_845998,Human_RBP_ID_18960940,Human_RBP_ID_26795085 RMVar_hsa_circ_124231,RMVar_hsa_circ_252352 92165 RMVar_ID_92165 Human_SNP_ID_366017635 m1A Human chr8 + 63169380 63169380 63169380 TTTTCTCCTCTTTACCGCATCTTTCGTCTTGCAACACAGAGACCTAAAGGGCAAGGAAATAAAGG TTTTCTCCTCTTTACCGCATCTTTCGTCTTGCGACACAGAGACCTAAAGGGCAAGGAAATAAAGG A G YTHDF3 Ensembl:ENSG00000185728 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:63169376..63169425 26863196 MeRIP-seq:(Medium) rs368771863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957780,Human_RBP_ID_9351595,Human_RBP_ID_19140219,Human_RBP_ID_24563389,Human_RBP_ID_26188985 Human_Splice_Rec_981423,Human_Splice_Rec_981433,Human_Splice_Rec_981441,Human_Splice_Rec_981445,Human_Splice_Rec_981453,Human_Splice_Rec_981461,Human_Splice_Rec_981467,Human_Splice_Rec_981477,Human_Splice_Rec_981487,Human_Splice_Rec_981491,Human_Splice_Rec_981497,Human_Splice_Rec_981503,Human_Splice_Rec_981509,Human_Splice_Rec_981517 RMVar_hsa_circ_124231,RMVar_hsa_circ_252352 92166 RMVar_ID_92166 Human_SNP_ID_366029332 m1A Human chr8 + 63212006 63212006 63212006 TCCTCTGAATGAAATTATCACAGGTTGTCTCAAGCACAACCAACTGAATGTCTCTTAACTGTGGG TCCTCTGAATGAAATTATCACAGGTTGTCTCAGGCACAACCAACTGAATGTCTCTTAACTGTGGG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs998816549 Functional Loss SNV dbSNP153 33..33 33 - - - 92167 RMVar_ID_92167 Human_SNP_ID_366623100 m1A Human chr8 + 65644783 65644783 65644783 AGCCGGAGAGGGTGCTGGCTGCCGCGCGGCCGAGGTGAGTAGGGTGGGAACTCGGAAAAGCGGTT AGCCGGAGAGGGTGCTGGCTGCCGCGCGGCCGGGGTGAGTAGGGTGGGAACTCGGAAAAGCGGTT A G MTFR1 Ensembl:ENSG00000066855 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:65644754..65644866;chr8:65644758..65644914 26863196 MeRIP-seq:(Medium) rs1183593742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995549,Human_RBP_ID_23087951 Human_Splice_Rec_981839,Human_Splice_Rec_981851,Human_Splice_Rec_981861,Human_Splice_Rec_981869,Human_Splice_Rec_981883 RMVar_hsa_circ_110390,RMVar_hsa_circ_252366 92168 RMVar_ID_92168 Human_SNP_ID_366665138 m1A Human chr8 - 65819809 65819809 65819809 CGGCTATGCCTACCTATAAGGGAGGCTGGGAAATGGAGCCTATGTGACTGATTGTATGCTCAGGA CGGCTATGCCTACCTATAAGGGAGGCTGGGAAGTGGAGCCTATGTGACTGATTGTATGCTCAGGA T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:65819776..65819933 26863196 MeRIP-seq:(Medium) rs904296250 Functional Loss SNV dbSNP153 33..33 33 - - - 92169 RMVar_ID_92169 Human_SNP_ID_366670532 m1A Human chr8 + 65841837 65841835 65841838 GAACCCCGCCGCCCTGGGGCTCCTCGGCCGAGAGGAGCAGGTACCCGGACTGCAGAGTTCGAGCG GAACCCCGCCGCCCTGGGGCTCCTCGGCCGA___GAGCAGGTACCCGGACTGCAGAGTTCGAGCG AGAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:65841788..65842511 26863196 MeRIP-seq:(Medium) rs1229167747 Functional Loss DEL dbSNP153 32..34 33 - - - 92170 RMVar_ID_92170 Human_SNP_ID_366736478 m1A Human chr8 - 66113425 66113425 66113425 CTTCGAGCCGGAATCGAACCAGCGACCTAAGGATGTCTCCTGCTGAGGAAGTAGCTACAGTCCTC CTTCGAGCCGGAATCGAACCAGCGACCTAAGGTTGTCTCCTGCTGAGGAAGTAGCTACAGTCCTC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr8:66113376..66113502;chr8:66113365..66113501;chr8:66113376..66113541;chr8:66113340..66113505 26863196 MeRIP-seq:(Medium) rs886490483 Functional Loss SNV dbSNP153 33..33 33 - - - 92171 RMVar_ID_92171 Human_SNP_ID_366736975 m1A Human chr8 - 66114205 66114205 66114205 CTACCTCTCGCATGCTAAGCGAGCGCTCTACCATTTGAGCTAATCCCCCACGGCTGGGCACGGCT CTACCTCTCGCATGCTAAGCGAGCGCTCTACCTTTTGAGCTAATCCCCCACGGCTGGGCACGGCT T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:66114188..66114272 26863410 MeRIP-seq:(Medium) rs1326183217 Functional Loss SNV dbSNP153 33..33 33 - - - 92172 RMVar_ID_92172 Human_SNP_ID_366736976 m1A Human chr8 - 66114205 66114205 66114205 CTACCTCTCGCATGCTAAGCGAGCGCTCTACCATTTGAGCTAATCCCCCACGGCTGGGCACGGCT CTACCTCTCGCATGCTAAGCGAGCGCTCTACCCTTTGAGCTAATCCCCCACGGCTGGGCACGGCT T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:66114188..66114272 26863410 MeRIP-seq:(Medium) rs1326183217 Functional Loss SNV dbSNP153 33..33 33 - - - 92173 RMVar_ID_92173 Human_SNP_ID_366736984 m1A Human chr8 + 66114209 66114209 66114209 GTGCCCAGCCGTGGGGGATTAGCTCAAATGGTAGAGCGCTCGCTTAGCATGCGAGAGGTAGCGGG GTGCCCAGCCGTGGGGGATTAGCTCAAATGGTGGAGCGCTCGCTTAGCATGCGAGAGGTAGCGGG A G AC084082.1 Ensembl:ENSG00000253190 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:66114189..66114285 26863410 MeRIP-seq:(Medium) rs977450892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1224912,Human_RBP_ID_1698630,Human_RBP_ID_5270885,Human_RBP_ID_8689715,Human_RBP_ID_16457081,Human_RBP_ID_17434774,Human_RBP_ID_18212048,Human_RBP_ID_18898587,Human_RBP_ID_22837152,Human_RBP_ID_23112172,Human_RBP_ID_23117152,Human_RBP_ID_23140961,Human_RBP_ID_26752132 92174 RMVar_ID_92174 Human_SNP_ID_366737033 m1A Human chr8 + 66114246 66114246 66114246 GCTCGCTTAGCATGCGAGAGGTAGCGGGATCGATGCCCGCATCCTCCAGTTTTCCTTCCTGTCCC GCTCGCTTAGCATGCGAGAGGTAGCGGGATCGGTGCCCGCATCCTCCAGTTTTCCTTCCTGTCCC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs1002540494 Functional Loss SNV dbSNP153 33..33 33 - - - 92175 RMVar_ID_92175 Human_SNP_ID_366737055 m1A Human chr8 - 66114269 66114267 66114269 GAGAATCGAAAGAAAAACCGTACGGGACAGGAAGGAAAACTGGAGGATGCGGGCATCGATCCCGC GAGAATCGAAAGAAAAACCGTACGGGACAGGA__GAAAACTGGAGGATGCGGGCATCGATCCCGC CCT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:66114183..66114292 26863410 MeRIP-seq:(Medium) rs1373129065 Functional Loss DEL dbSNP153 33..34 33 - - - 92176 RMVar_ID_92176 Human_SNP_ID_366737059 m1A Human chr8 - 66114269 66114269 66114269 GAGAATCGAAAGAAAAACCGTACGGGACAGGAAGGAAAACTGGAGGATGCGGGCATCGATCCCGC GAGAATCGAAAGAAAAACCGTACGGGACAGGAGGGAAAACTGGAGGATGCGGGCATCGATCCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:66114183..66114292 26863410 MeRIP-seq:(Medium) rs1391388659 Functional Loss SNV dbSNP153 33..33 33 - - - 92177 RMVar_ID_92177 Human_SNP_ID_366812513 m1A Human chr8 + 66430062 66430062 66430062 CCGCCAAGAGGAGGAAAATGAGCCAGAAGGGCAAGAGAAAGGGAGGCCGGCAGGGGCCTGGGGGC CCGCCAAGAGGAGGAAAATGAGCCAGAAGGGCGAGAGAAAGGGAGGCCGGCAGGGGCCTGGGGGC A G RRS1 Ensembl:ENSG00000179041 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:66429926..66430250;chr8:66429817..66430346 26863196 MeRIP-seq:(Medium) rs575683969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15106,Human_RBP_ID_255498,Human_RBP_ID_4990211 92178 RMVar_ID_92178 Human_SNP_ID_366853547 m1A Human chr8 + 66602511 66602511 66602511 TCATAATCATGATCGGCATACTGAAGGTCATCATCCTCATCCTCACTACAAAAAAAACACAATTT TCATAATCATGATCGGCATACTGAAGGTCATCCTCCTCATCCTCACTACAAAAAAAACACAATTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:66602460..66612550 26863196 MeRIP-seq:(Medium) rs367791059 Functional Loss SNV dbSNP153 33..33 33 - - - 92179 RMVar_ID_92179 Human_SNP_ID_366855985 m1A Human chr8 - 66612854 66612854 66612854 GGCTGACCCGCGTCCCCGCCCAGCCTGCTCCTATGCGGTACTTGAAGGATGGCGAAGAGGTCGCG GGCTGACCCGCGTCCCCGCCCAGCCTGCTCCTGTGCGGTACTTGAAGGATGGCGAAGAGGTCGCG T C MYBL1 Ensembl:ENSG00000185697 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:66602460..66613074 32194978 MeRIP-seq:(Medium) rs1487667250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4990236 Human_Splice_Rec_982591,Human_Splice_Rec_982619,Human_Splice_Rec_982639 92180 RMVar_ID_92180 Human_SNP_ID_366855986 m1A Human chr8 - 66612854 66612854 66612854 GGCTGACCCGCGTCCCCGCCCAGCCTGCTCCTATGCGGTACTTGAAGGATGGCGAAGAGGTCGCG GGCTGACCCGCGTCCCCGCCCAGCCTGCTCCTCTGCGGTACTTGAAGGATGGCGAAGAGGTCGCG T G MYBL1 Ensembl:ENSG00000185697 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:66602460..66613074 32194978 MeRIP-seq:(Medium) rs1487667250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4990236 Human_Splice_Rec_982591,Human_Splice_Rec_982619,Human_Splice_Rec_982639 92181 RMVar_ID_92181 Human_SNP_ID_366856089 m1A Human chr8 + 66613159 66613159 66613159 CCGCCGCTTGTCAGCCTCCCTGCCCTGGCCCCAGCCCGGCTCCGCCACAGGCGCCCGACCCCTGC CCGCCGCTTGTCAGCCTCCCTGCCCTGGCCCCGGCCCGGCTCCGCCACAGGCGCCCGACCCCTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:66612800..66613300 26863196 MeRIP-seq:(Medium) rs1229489125 Functional Loss SNV dbSNP153 33..33 33 - - - 92182 RMVar_ID_92182 Human_SNP_ID_366856124 m1A Human chr8 - 66613235 66613235 66613235 CGCGAGATTCGGCGGTGCGGACAAAACCCTGCAGGAGACTGCGAGCCCTGCAGAACTGCTAGCTG CGCGAGATTCGGCGGTGCGGACAAAACCCTGCGGGAGACTGCGAGCCCTGCAGAACTGCTAGCTG T C MYBL1 Ensembl:ENSG00000185697 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr8:66612828..66613294;chr8:66612926..66613275 26863196 MeRIP-seq:(Medium) rs922680136 Functional Loss SNV dbSNP153 33..33 33 - - - 92183 RMVar_ID_92183 Human_SNP_ID_366869310 m1A Human chr8 + 66667006 66667006 66667006 TGTCTCGCTCCGCGTCCCAGGCGACCCTCAAAAGCTCATAGCCCAGACCCCCACCAACCCGACTC TGTCTCGCTCCGCGTCCCAGGCGACCCTCAAACGCTCATAGCCCAGACCCCCACCAACCCGACTC A C RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:66666847..66667201 26863196 MeRIP-seq:(Medium) rs552325432 Functional Loss SNV dbSNP153 33..33 33 - - - 92184 RMVar_ID_92184 Human_SNP_ID_366869311 m1A Human chr8 + 66667006 66667006 66667006 TGTCTCGCTCCGCGTCCCAGGCGACCCTCAAAAGCTCATAGCCCAGACCCCCACCAACCCGACTC TGTCTCGCTCCGCGTCCCAGGCGACCCTCAAAGGCTCATAGCCCAGACCCCCACCAACCCGACTC A G RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:66666847..66667201 26863196 MeRIP-seq:(Medium) rs552325432 Functional Loss SNV dbSNP153 33..33 33 - - - 92185 RMVar_ID_92185 Human_SNP_ID_366869541 m1A Human chr8 - 66667653 66667653 66667653 CTTTCCACTCCCCTCCCCTTCTAGTAGTCGTGAACTTCAGACCCTCGCTTCGACTCCCACTGCCA CTTTCCACTCCCCTCCCCTTCTAGTAGTCGTGGACTTCAGACCCTCGCTTCGACTCCCACTGCCA T C RF00017-7091 RNACentral:URS0000905735 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:66667602..66679763;chr8:66667605..66667767 26863196 MeRIP-seq:(Medium) rs1051189116 Functional Loss SNV dbSNP153 33..33 33 - - - 92186 RMVar_ID_92186 Human_SNP_ID_366880635 m1A Human chr8 + 66712783 66712783 66712783 GCCCGGCGGCCCTGCCGGGAAGGAGGAAGCGCAGTGCGTTCGGCTCCGCGCCCGCCGCGCCGGGA GCCCGGCGGCCCTGCCGGGAAGGAGGAAGCGCGGTGCGTTCGGCTCCGCGCCCGCCGCGCCGGGA A G SGK3,C8orf44-SGK3 Ensembl:ENSG00000104205,Ensembl:ENSG00000288602 Protein coding,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:66712555..66712835 26863196 MeRIP-seq:(Medium) rs1342143312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959185 Human_Splice_Rec_982749,Human_Splice_Rec_982757,Human_Splice_Rec_982759 92187 RMVar_ID_92187 Human_SNP_ID_366880735 m1A Human chr8 + 66713096 66713096 66713096 GCTGGACCTTGTTAACCCCCACGCAGCCGCCGAGCCTGGAGGAACTGGGAACGCCGAGCAGGGAG GCTGGACCTTGTTAACCCCCACGCAGCCGCCGTGCCTGGAGGAACTGGGAACGCCGAGCAGGGAG A T SGK3,C8orf44-SGK3 Ensembl:ENSG00000104205,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:66713064..66713212 26863196 MeRIP-seq:(Medium) rs1227255099 Functional Loss SNV dbSNP153 33..33 33 - - - 92188 RMVar_ID_92188 Human_SNP_ID_366915986 m1A Human chr8 + 66861417 66861417 66861417 ATCACTTGAGCCTATGAGTTCAAGACCAGCCTAGGCAATGTAGTGACACCTCATTTCTATTTATT ATCACTTGAGCCTATGAGTTCAAGACCAGCCTGGGCAATGTAGTGACACCTCATTTCTATTTATT A G SGK3 Ensembl:ENSG00000104205 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7815142 Functional Loss SNV dbSNP153 33..33 33 - - - 92189 RMVar_ID_92189 Human_SNP_ID_366929768 m1A Human chr8 + 66922339 66922339 66922339 CTTGACAAATCACTTACTTGAGGTAACGAAGCAGAAGTATTTTTAAACATGACAGCTAAGAACAT CTTGACAAATCACTTACTTGAGGTAACGAAGCGGAAGTATTTTTAAACATGACAGCTAAGAACAT A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:66921982..66922338 32194978 MeRIP-seq:(Medium) rs1248362275 Functional Loss SNV dbSNP153 33..33 33 - - - 92190 RMVar_ID_92190 Human_SNP_ID_366930552 m1A Human chr8 - 66925515 66925515 66925515 CTCTTCCTTTCCCGCGCGACCGGCGAGGGAGGAAGAAGCGCGAAGAGCCGTTAGTCATGCCGGTG CTCTTCCTTTCCCGCGCGACCGGCGAGGGAGGGAGAAGCGCGAAGAGCCGTTAGTCATGCCGGTG T C SNHG6 Ensembl:ENSG00000245910 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs536644508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_703046,Human_RBP_ID_796817,Human_RBP_ID_844834,Human_RBP_ID_1700166,Human_RBP_ID_4995556,Human_RBP_ID_5090865,Human_RBP_ID_5106751,Human_RBP_ID_5641193,Human_RBP_ID_5658392,Human_RBP_ID_8223084,Human_RBP_ID_18426706,Human_RBP_ID_22332590,Human_RBP_ID_23088098,Human_RBP_ID_24549563 Human_Splice_Rec_983129,Human_Splice_Rec_983133,Human_Splice_Rec_983139,Human_Splice_Rec_983149 92191 RMVar_ID_92191 Human_SNP_ID_366984142 m1A Human chr8 - 67158523 67158523 67158523 ACTCCTGCTGAATTCGTGCCCTCTGTTCTGCAAGCCGTCTTTCTTCTTTTTCTTCTGCAATTCTC ACTCCTGCTGAATTCGTGCCCTCTGTTCTGCAGGCCGTCTTTCTTCTTTTTCTTCTGCAATTCTC T C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:67158474..67158638 26863196 MeRIP-seq:(Medium) rs778324209 Functional Loss SNV dbSNP153 33..33 33 - - - 92192 RMVar_ID_92192 Human_SNP_ID_366984162 m1A Human chr8 + 67158579 67158578 67158580 AGCAGGAGTATGAAGAGGAACAGGAAAAGAAAAGAGAGAAAGAGGAGGAGGTACATCTTTTTTCC AGCAGGAGTATGAAGAGGAACAGGAAAAGAAA__AGAGAAAGAGGAGGAGGTACATCTTTTTTCC AAG A CSPP1 Ensembl:ENSG00000104218 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:67158465..67158650 26863196 MeRIP-seq:(Medium) rs1375090095 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24549385 Human_Splice_Rec_983423,Human_Splice_Rec_983493,Human_Splice_Rec_983523,Human_Splice_Rec_983545 RMVar_hsa_circ_7486,RMVar_hsa_circ_365717,RMVar_hsa_circ_58093,RMVar_hsa_circ_58565,RMVar_hsa_circ_356456,RMVar_hsa_circ_326067,RMVar_hsa_circ_355060,RMVar_hsa_circ_350678,RMVar_hsa_circ_316576,RMVar_hsa_circ_125750,RMVar_hsa_circ_60609,RMVar_hsa_circ_252481,RMVar_hsa_circ_45641,RMVar_hsa_circ_367747,RMVar_hsa_circ_62091,RMVar_hsa_circ_29849,RMVar_hsa_circ_252494,RMVar_hsa_circ_366704,RMVar_hsa_circ_358910,RMVar_hsa_circ_312072,RMVar_hsa_circ_323307,RMVar_hsa_circ_330321,RMVar_hsa_circ_324673,RMVar_hsa_circ_313413,RMVar_hsa_circ_293911,RMVar_hsa_circ_122910,RMVar_hsa_circ_252496,RMVar_hsa_circ_252495,RMVar_hsa_circ_61044,RMVar_hsa_circ_304846,RMVar_hsa_circ_354711,RMVar_hsa_circ_359086,RMVar_hsa_circ_252493,RMVar_hsa_circ_364833,RMVar_hsa_circ_354912,RMVar_hsa_circ_350717,RMVar_hsa_circ_69878,RMVar_hsa_circ_299921,RMVar_hsa_circ_303783,RMVar_hsa_circ_363845,RMVar_hsa_circ_364023,RMVar_hsa_circ_339691,RMVar_hsa_circ_295302,RMVar_hsa_circ_9577,RMVar_hsa_circ_58455,RMVar_hsa_circ_252505,RMVar_hsa_circ_252506,RMVar_hsa_circ_252504,RMVar_hsa_circ_327453,RMVar_hsa_circ_335876,RMVar_hsa_circ_338038,RMVar_hsa_circ_352866,RMVar_hsa_circ_333165,RMVar_hsa_circ_51791,RMVar_hsa_circ_342024,RMVar_hsa_circ_252508,RMVar_hsa_circ_252509,RMVar_hsa_circ_252507,RMVar_hsa_circ_344183,RMVar_hsa_circ_59501,RMVar_hsa_circ_314819,RMVar_hsa_circ_56761 92193 RMVar_ID_92193 Human_SNP_ID_366989557 m1A Human chr8 + 67178638 67178638 67178638 TACAGTGGGCATGGGGGCTCACTGGGTAGGCAACATTTGAGTAAGGACATCAGGGAGGTGTCTAT TACAGTGGGCATGGGGGCTCACTGGGTAGGCATCATTTGAGTAAGGACATCAGGGAGGTGTCTAT A T CSPP1 Ensembl:ENSG00000104218 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:67178615..67178802;chr8:67178484..67178773 26863196 MeRIP-seq:(Medium) rs1347331596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7851907 RMVar_hsa_circ_7486,RMVar_hsa_circ_58093,RMVar_hsa_circ_355060,RMVar_hsa_circ_350678,RMVar_hsa_circ_125750,RMVar_hsa_circ_252481,RMVar_hsa_circ_312072,RMVar_hsa_circ_313413,RMVar_hsa_circ_252493,RMVar_hsa_circ_364833,RMVar_hsa_circ_354912,RMVar_hsa_circ_363845,RMVar_hsa_circ_364023,RMVar_hsa_circ_327453,RMVar_hsa_circ_338038,RMVar_hsa_circ_252507,RMVar_hsa_circ_344183,RMVar_hsa_circ_252510,RMVar_hsa_circ_318310,RMVar_hsa_circ_367203,RMVar_hsa_circ_252511,RMVar_hsa_circ_313783,RMVar_hsa_circ_323991,RMVar_hsa_circ_252513,RMVar_hsa_circ_89490,RMVar_hsa_circ_252516,RMVar_hsa_circ_311572,RMVar_hsa_circ_334062,RMVar_hsa_circ_356506,RMVar_hsa_circ_252515,RMVar_hsa_circ_323902,RMVar_hsa_circ_252517,RMVar_hsa_circ_252518 92194 RMVar_ID_92194 Human_SNP_ID_366996160 m1A Human chr8 + 67203448 67203448 67203448 TCGTCCCCAAGCACCACCTCCCATTAGTCCAGACCCTCCTGGACTCCCAACTCCCTGGCCCTGCG TCGTCCCCAAGCACCACCTCCCATTAGTCCAGGCCCTCCTGGACTCCCAACTCCCTGGCCCTGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:67203401..67203589 26863196 MeRIP-seq:(Medium) rs1478386233 Functional Loss SNV dbSNP153 33..33 33 - - - 92195 RMVar_ID_92195 Human_SNP_ID_366996165 m1A Human chr8 + 67203464 67203457 67203464 CCTCCCATTAGTCCAGACCCTCCTGGACTCCCAACTCCCTGGCCCTGCGTTCCTCAGCCCCTCAA CCTCCCATTAGTCCAGACCCTCCTGG_______ACTCCCTGGCCCTGCGTTCCTCAGCCCCTCAA GACTCCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:67203419..67203598 26863196 MeRIP-seq:(Medium) rs1209880627 Functional Loss DEL dbSNP153 27..33 33 - - - 92196 RMVar_ID_92196 Human_SNP_ID_366996169 m1A Human chr8 + 67203464 67203464 67203464 CCTCCCATTAGTCCAGACCCTCCTGGACTCCCAACTCCCTGGCCCTGCGTTCCTCAGCCCCTCAA CCTCCCATTAGTCCAGACCCTCCTGGACTCCCTACTCCCTGGCCCTGCGTTCCTCAGCCCCTCAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:67203419..67203598 26863196 MeRIP-seq:(Medium) rs982297955 Functional Loss SNV dbSNP153 33..33 33 - - - 92197 RMVar_ID_92197 Human_SNP_ID_367030477 m1A Human chr8 - 67337498 67337498 67337498 CATGTTTATGTTTTTAAAGGCTCACTGTGGCCAGAGACCATGGGGACTTAGGCTAAGTTGGTGGT CATGTTTATGTTTTTAAAGGCTCACTGTGGCCGGAGACCATGGGGACTTAGGCTAAGTTGGTGGT T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:67337495..67337641 26863196 MeRIP-seq:(Medium) rs779644801 Functional Loss SNV dbSNP153 33..33 33 - - - 92198 RMVar_ID_92198 Human_SNP_ID_367032163 m1A Human chr8 + 67343361 67343361 67343361 CCCAGCGGCTGGAGGGGAGGAGGAGGAGAGGAAGGAAGAGAAGAGAGAAAGGAGAGGGGGTGGAG CCCAGCGGCTGGAGGGGAGGAGGAGGAGAGGATGGAAGAGAAGAGAGAAAGGAGAGGGGGTGGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:67343311..67343406 26863196 MeRIP-seq:(Medium) rs1458306186 Functional Loss SNV dbSNP153 33..33 33 - - - 92199 RMVar_ID_92199 Human_SNP_ID_367032172 m1A Human chr8 + 67343377 67343377 67343377 GAGGAGGAGGAGAGGAAGGAAGAGAAGAGAGAAAGGAGAGGGGGTGGAGGTGGGGGATTGGAGGC GAGGAGGAGGAGAGGAAGGAAGAGAAGAGAGACAGGAGAGGGGGTGGAGGTGGGGGATTGGAGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:67343327..67343428 26863196 MeRIP-seq:(Medium) rs997402398 Functional Loss SNV dbSNP153 33..33 33 - - - 92200 RMVar_ID_92200 Human_SNP_ID_367032186 m1A Human chr8 - 67343402 67343402 67343402 TCCTGATCCTGCCGCTGCCCTCCACGCCTCCAATCCCCCACCTCCACCCCCTCTCCTTTCTCTCT TCCTGATCCTGCCGCTGCCCTCCACGCCTCCAGTCCCCCACCTCCACCCCCTCTCCTTTCTCTCT T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:67343276..67343489 26863196 MeRIP-seq:(Medium) rs1212910489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18961537 92201 RMVar_ID_92201 Human_SNP_ID_367265401 m1A Human chr8 - 68306413 68306413 68306413 CGCTGGGGAGGTGGAGCATGAGCACAGGTGTTAGGAAATGAAAGATTGTGAACTATGCCTGGGCA CGCTGGGGAGGTGGAGCATGAGCACAGGTGTTGGGAAATGAAAGATTGTGAACTATGCCTGGGCA T C C8orf34-AS1 Ensembl:ENSG00000248801 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:68306226..68306541 26863196 MeRIP-seq:(Medium) rs1206506260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7852344,Human_RBP_ID_8156589,Human_RBP_ID_8921445,Human_RBP_ID_9230525,Human_RBP_ID_16462727,Human_RBP_ID_17053712,Human_RBP_ID_17318586,Human_RBP_ID_17433225,Human_RBP_ID_17715125,Human_RBP_ID_18125840,Human_RBP_ID_21953612,Human_RBP_ID_26752047,Human_RBP_ID_27162104 92202 RMVar_ID_92202 Human_SNP_ID_367388535 m1A Human chr8 - 68813633 68813633 68813633 GTGCTTGGCACAGGGCAATGGAGAGAAGCAACAGCTTCCTCTGGAGGAGGCTAACAGGGACCCAA GTGCTTGGCACAGGGCAATGGAGAGAAGCAACGGCTTCCTCTGGAGGAGGCTAACAGGGACCCAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:68813630..68813715 32194978 MeRIP-seq:(Medium) rs907258634 Functional Loss SNV dbSNP153 33..33 33 - - - 92203 RMVar_ID_92203 Human_SNP_ID_367468468 m1A Human chr8 - 69129994 69129994 69129994 CACGCTCCTCTGCCCTCTCCAGCTCACCCTCCAGGATGACCAGCTTACGAGCTACCTTCTCGTAT CACGCTCCTCTGCCCTCTCCAGCTCACCCTCCGGGATGACCAGCTTACGAGCTACCTTCTCGTAT T C lnc-SLCO5A1-8 RNACentral:URS00008B4F17 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:69129830..69130009 26863196 MeRIP-seq:(Medium) rs540707911 Functional Loss SNV dbSNP153 33..33 33 - - - 92204 RMVar_ID_92204 Human_SNP_ID_367745036 m1A Human chr8 - 70237317 70237317 70237317 TAATGAGGCAGTGTCCTAGAGGTAAAGAGTACAGGCTTAGAGTCAGACAGCGCGGGTTCAAATCC TAATGAGGCAGTGTCCTAGAGGTAAAGAGTACGGGCTTAGAGTCAGACAGCGCGGGTTCAAATCC T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:70237297..70237433 26863196 MeRIP-seq:(Medium) rs139259883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16463653 RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_106213,RMVar_hsa_circ_252651,RMVar_hsa_circ_72919,RMVar_hsa_circ_252669,RMVar_hsa_circ_289573 92205 RMVar_ID_92205 Human_SNP_ID_367785113 m1A Human chr8 - 70403337 70403337 70403337 GCGGGCGGAGGCTGCAGCCCGCGGCGCGGGCGAGAGGTGAGCGCCGAGGCGCGGCCGGGGGTGCG GCGGGCGGAGGCTGCAGCCCGCGGCGCGGGCGGGAGGTGAGCGCCGAGGCGCGGCCGGGGGTGCG T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:70402780..70403425 26863196 MeRIP-seq:(Medium) rs1005630436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885820,Human_RBP_ID_4990786,Human_RBP_ID_8238697,Human_RBP_ID_9441428,Human_RBP_ID_22732264,Human_RBP_ID_23088049 RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_106213,RMVar_hsa_circ_252651 92206 RMVar_ID_92206 Human_SNP_ID_367834413 m1A Human chr8 + 70608224 70608224 70608224 ATCGCCATGGTGGGGCCGCCGCCCGCGCCTGCAGGTGCTCCGCCCCGGTTCTGCTCTTCCCAGCT ATCGCCATGGTGGGGCCGCCGCCCGCGCCTGCCGGTGCTCCGCCCCGGTTCTGCTCTTCCCAGCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:70608076..70608288 32194978 MeRIP-seq:(Medium) rs1386372904 Functional Loss SNV dbSNP153 33..33 33 - - - 92207 RMVar_ID_92207 Human_SNP_ID_367834433 m1A Human chr8 - 70608256 70608255 70608256 AGCCAGCGGGAGGCGGCGGCGAGTCGGTGAGCAGCTGGGAAGAGCAGAACCGGGGCGGAGCACCT AGCCAGCGGGAGGCGGCGGCGAGTCGGTGAGC_GCTGGGAAGAGCAGAACCGGGGCGGAGCACCT CT C TRAM1 Ensembl:ENSG00000067167 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:70608215..70608361 26863196 MeRIP-seq:(Medium) rs1324476834 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_795304,Human_RBP_ID_844745,Human_RBP_ID_961109,Human_RBP_ID_4995077,Human_RBP_ID_5153904,Human_RBP_ID_5329141,Human_RBP_ID_16467428,Human_RBP_ID_22465231 RMVar_hsa_circ_93562,RMVar_hsa_circ_252673,RMVar_hsa_circ_101158,RMVar_hsa_circ_252694 92208 RMVar_ID_92208 Human_SNP_ID_367834445 m1A Human chr8 - 70608288 70608288 70608288 CAGCGAGCGGCTGCAGCGGGGCCGTGAGGAGCAGCCAGCGGGAGGCGGCGGCGAGTCGGTGAGCA CAGCGAGCGGCTGCAGCGGGGCCGTGAGGAGCCGCCAGCGGGAGGCGGCGGCGAGTCGGTGAGCA T G TRAM1 Ensembl:ENSG00000067167 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:70608144..70608375;chr8:70608187..70608337;chr8:70608076..70608389;chr8:70608076..70608375 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1194279471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795304,Human_RBP_ID_844745,Human_RBP_ID_961109,Human_RBP_ID_4995077,Human_RBP_ID_5329141,Human_RBP_ID_22465231,Human_RBP_ID_22837212 Human_Splice_Rec_984985 RMVar_hsa_circ_93562,RMVar_hsa_circ_252673,RMVar_hsa_circ_101158,RMVar_hsa_circ_252694 92209 RMVar_ID_92209 Human_SNP_ID_367834446 m1A Human chr8 - 70608291 70608291 70608291 CCCCAGCGAGCGGCTGCAGCGGGGCCGTGAGGAGCAGCCAGCGGGAGGCGGCGGCGAGTCGGTGA CCCCAGCGAGCGGCTGCAGCGGGGCCGTGAGGCGCAGCCAGCGGGAGGCGGCGGCGAGTCGGTGA T G TRAM1 Ensembl:ENSG00000067167 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:70608126..70608375 26863196 MeRIP-seq:(Medium) rs1380131415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795304,Human_RBP_ID_844745,Human_RBP_ID_961109,Human_RBP_ID_4990856,Human_RBP_ID_5329141,Human_RBP_ID_22465231,Human_RBP_ID_22837212 Human_Splice_Rec_984985 RMVar_hsa_circ_93562,RMVar_hsa_circ_252673,RMVar_hsa_circ_101158,RMVar_hsa_circ_252694 92210 RMVar_ID_92210 Human_SNP_ID_368307008 m1A Human chr8 - 72537374 72537373 72537374 AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGGAGGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGG_GGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:72537330..72537443 26863196 MeRIP-seq:(Medium) rs1289192460 Functional Loss DEL dbSNP153 33..33 33 - - - 92211 RMVar_ID_92211 Human_SNP_ID_368307010 m1A Human chr8 - 72537374 72537374 72537374 AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGGAGGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGGGGGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:72537330..72537443 26863196 MeRIP-seq:(Medium) rs1298253835 Functional Loss SNV dbSNP153 33..33 33 - - - 92212 RMVar_ID_92212 Human_SNP_ID_368307011 m1A Human chr8 - 72537374 72537374 72537374 AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGGAGGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT AGGCGCAGCGGCGGCGGCGGCCGCGGGGGCGGCGGGCGGAGGGCGGAGGGCGGTGGGTGCTTGGT T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:72537330..72537443 26863196 MeRIP-seq:(Medium) rs1298253835 Functional Loss SNV dbSNP153 33..33 33 - - - 92213 RMVar_ID_92213 Human_SNP_ID_368414199 m1A Human chr8 - 73008940 73008940 73008940 GCCATCTGCTCCTCAGTAGGGTCGGCATCCCTACCATCCGCACAGCCCCGCGGGCTCGGGGCCGC GCCATCTGCTCCTCAGTAGGGTCGGCATCCCTGCCATCCGCACAGCCCCGCGGGCTCGGGGCCGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:73008891..73009021 26863196 MeRIP-seq:(Medium) rs1304461214 Functional Loss SNV dbSNP153 33..33 33 - - - 92214 RMVar_ID_92214 Human_SNP_ID_368419730 m1A Human chr8 + 73030951 73030951 73030951 GAGGTGATTGGACATGAGGAACTGAGAGGCCAAGATGGTATATGAATTGTCTGTGAGAACACTGA GAGGTGATTGGACATGAGGAACTGAGAGGCCAGGATGGTATATGAATTGTCTGTGAGAACACTGA A G TERF1 Ensembl:ENSG00000147601 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:73030900..73031039 26863196 MeRIP-seq:(Medium) rs1354743765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16468393 RMVar_hsa_circ_68840,RMVar_hsa_circ_363284,RMVar_hsa_circ_335559,RMVar_hsa_circ_355960,RMVar_hsa_circ_363210 92215 RMVar_ID_92215 Human_SNP_ID_368484288 m1A Human chr8 - 73292751 73292751 73292751 AGGTTCCTGCTGTGCCAGAAACCCTTAAGAAAAAGCGAAGGAATTTCGCAGAGCTGAAGATCAAG AGGTTCCTGCTGTGCCAGAAACCCTTAAGAAAGAGCGAAGGAATTTCGCAGAGCTGAAGATCAAG T C RPL7 Ensembl:ENSG00000147604 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:73292676..73292825 26863410 MeRIP-seq:(Medium) rs11545448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26193785 Human_Splice_Rec_986026,Human_Splice_Rec_986027,Human_Splice_Rec_986040,Human_Splice_Rec_986041,Human_Splice_Rec_986050,Human_Splice_Rec_986051,Human_Splice_Rec_986060,Human_Splice_Rec_986061,Human_Splice_Rec_986072,Human_Splice_Rec_986073,Human_Splice_Rec_986078,Human_Splice_Rec_986079 RMVar_hsa_circ_76234,RMVar_hsa_circ_252730,RMVar_hsa_circ_68230 92216 RMVar_ID_92216 Human_SNP_ID_368484289 m1A Human chr8 - 73292751 73292751 73292751 AGGTTCCTGCTGTGCCAGAAACCCTTAAGAAAAAGCGAAGGAATTTCGCAGAGCTGAAGATCAAG AGGTTCCTGCTGTGCCAGAAACCCTTAAGAAACAGCGAAGGAATTTCGCAGAGCTGAAGATCAAG T G RPL7 Ensembl:ENSG00000147604 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:73292676..73292825 26863410 MeRIP-seq:(Medium) rs11545448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26193785 Human_Splice_Rec_986026,Human_Splice_Rec_986027,Human_Splice_Rec_986040,Human_Splice_Rec_986041,Human_Splice_Rec_986050,Human_Splice_Rec_986051,Human_Splice_Rec_986060,Human_Splice_Rec_986061,Human_Splice_Rec_986072,Human_Splice_Rec_986073,Human_Splice_Rec_986078,Human_Splice_Rec_986079 RMVar_hsa_circ_76234,RMVar_hsa_circ_252730,RMVar_hsa_circ_68230 92217 RMVar_ID_92217 Human_SNP_ID_368484308 m1A Human chr8 - 73292787 73292784 73292787 CATTTTTGTTTATTAACGTTAGAGAGAAGAAGAAGGAGGTTCCTGCTGTGCCAGAAACCCTTAAG CATTTTTGTTTATTAACGTTAGAGAGAAGAAG___GAGGTTCCTGCTGTGCCAGAAACCCTTAAG CCTT C RPL7 Ensembl:ENSG00000147604 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:73292654..73292825 26863410 MeRIP-seq:(Medium) rs556746526 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_254881,Human_RBP_ID_16469095,Human_RBP_ID_17665965,Human_RBP_ID_24391634,Human_RBP_ID_24549456,Human_RBP_ID_26181672 Human_Splice_Rec_986026,Human_Splice_Rec_986027,Human_Splice_Rec_986040,Human_Splice_Rec_986041,Human_Splice_Rec_986050,Human_Splice_Rec_986051,Human_Splice_Rec_986060,Human_Splice_Rec_986061,Human_Splice_Rec_986072,Human_Splice_Rec_986073,Human_Splice_Rec_986078,Human_Splice_Rec_986079 Human_miRNA_ID_2221270,Human_miRNA_ID_2484316,Human_miRNA_ID_3072695,Human_miRNA_ID_3088051 RMVar_hsa_circ_76234,RMVar_hsa_circ_252730,RMVar_hsa_circ_68230 92218 RMVar_ID_92218 Human_SNP_ID_368484310 m1A Human chr8 - 73292787 73292787 73292787 CATTTTTGTTTATTAACGTTAGAGAGAAGAAGAAGGAGGTTCCTGCTGTGCCAGAAACCCTTAAG CATTTTTGTTTATTAACGTTAGAGAGAAGAAGGAGGAGGTTCCTGCTGTGCCAGAAACCCTTAAG T C RPL7 Ensembl:ENSG00000147604 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:73292654..73292825 26863410 MeRIP-seq:(Medium) rs768798846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254881,Human_RBP_ID_16469095,Human_RBP_ID_17665965,Human_RBP_ID_24391634,Human_RBP_ID_24549456,Human_RBP_ID_26181672 Human_Splice_Rec_986026,Human_Splice_Rec_986027,Human_Splice_Rec_986040,Human_Splice_Rec_986041,Human_Splice_Rec_986050,Human_Splice_Rec_986051,Human_Splice_Rec_986060,Human_Splice_Rec_986061,Human_Splice_Rec_986072,Human_Splice_Rec_986073,Human_Splice_Rec_986078,Human_Splice_Rec_986079 Human_miRNA_ID_2221270,Human_miRNA_ID_2484316,Human_miRNA_ID_3072695,Human_miRNA_ID_3088051 RMVar_hsa_circ_76234,RMVar_hsa_circ_252730,RMVar_hsa_circ_68230 92219 RMVar_ID_92219 Human_SNP_ID_368485150 m1A Human chr8 + 73294648 73294648 73294648 GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGAGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGCGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG A C RDH10 Ensembl:ENSG00000121039 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73294600..73295400 26863196 MeRIP-seq:(Medium) rs1390901288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88371,Human_RBP_ID_254834,Human_RBP_ID_846032,Human_RBP_ID_4995079,Human_RBP_ID_5453719,Human_RBP_ID_5534221,Human_RBP_ID_22626527 Human_miRNA_ID_2553642,Human_miRNA_ID_2996280 RMVar_hsa_circ_107011,RMVar_hsa_circ_252735 92220 RMVar_ID_92220 Human_SNP_ID_368485151 m1A Human chr8 + 73294648 73294648 73294648 GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGAGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGGGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG A G RDH10 Ensembl:ENSG00000121039 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73294600..73295400 26863196 MeRIP-seq:(Medium) rs1390901288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88371,Human_RBP_ID_254834,Human_RBP_ID_846032,Human_RBP_ID_4995079,Human_RBP_ID_5453719,Human_RBP_ID_5534221,Human_RBP_ID_22626527 Human_miRNA_ID_2553642,Human_miRNA_ID_2996280 RMVar_hsa_circ_107011,RMVar_hsa_circ_252735 92221 RMVar_ID_92221 Human_SNP_ID_368485152 m1A Human chr8 + 73294648 73294648 73294648 GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGAGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG GCGCTCTGACTTGCAAGCGGGCTGCGCTGCGGTGCCCAGTGCCCGAGTGACACCCGCGGAGAGTG A T RDH10 Ensembl:ENSG00000121039 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73294600..73295400 26863196 MeRIP-seq:(Medium) rs1390901288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88371,Human_RBP_ID_254834,Human_RBP_ID_846032,Human_RBP_ID_4995079,Human_RBP_ID_5453719,Human_RBP_ID_5534221,Human_RBP_ID_22626527 Human_miRNA_ID_2553642,Human_miRNA_ID_2996280 RMVar_hsa_circ_107011,RMVar_hsa_circ_252735 92222 RMVar_ID_92222 Human_SNP_ID_368485285 m1A Human chr8 + 73295043 73295043 73295043 GACGGGCGGGCGGCTGCCGGCAGGAGGCGCCGAGCCGGGTGACTGCCGCGGCGGGCACAGTCCGG GACGGGCGGGCGGCTGCCGGCAGGAGGCGCCGTGCCGGGTGACTGCCGCGGCGGGCACAGTCCGG A T RDH10 Ensembl:ENSG00000121039 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:73294551..73295522 26863196 MeRIP-seq:(Medium) rs985638120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254836,Human_RBP_ID_846034,Human_RBP_ID_4995082,Human_RBP_ID_5515105,Human_RBP_ID_5534223 Human_miRNA_ID_2017781,Human_miRNA_ID_3115059 RMVar_hsa_circ_107011,RMVar_hsa_circ_252735 92223 RMVar_ID_92223 Human_SNP_ID_368592718 m1A Human chr8 + 73746200 73746200 73746200 ATTTCGGCAAGTTACGTCTTTACCACTAGCCCATTCTACAGAAATAGCTGCCGCCGCCACCCTCC ATTTCGGCAAGTTACGTCTTTACCACTAGCCCGTTCTACAGAAATAGCTGCCGCCGCCACCCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73746195..73746512 26863196 MeRIP-seq:(Medium) rs1357276226 Functional Loss SNV dbSNP153 33..33 33 - - - 92224 RMVar_ID_92224 Human_SNP_ID_368592763 m1A Human chr8 + 73746349 73746349 73746349 TACTCTAGGCGCTCCCTCTCCCTCGCAGCCACACCGTGGCTGCACTCGCCGTCCTCTCTTCCGGC TACTCTAGGCGCTCCCTCTCCCTCGCAGCCACCCCGTGGCTGCACTCGCCGTCCTCTCTTCCGGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:73746253..73746446 26863196 MeRIP-seq:(Medium) rs1224211180 Functional Loss SNV dbSNP153 33..33 33 - - - 92225 RMVar_ID_92225 Human_SNP_ID_368627007 m1A Human chr8 - 73878727 73878727 73878727 GTGCCAGCGTTCGGGCGGGGGTGGCGTCCGCGATTCGGGGACACCCGGGCGGGTTCGGGATCGGT GTGCCAGCGTTCGGGCGGGGGTGGCGTCCGCGGTTCGGGGACACCCGGGCGGGTTCGGGATCGGT T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:73878700..73878782 26863196 MeRIP-seq:(Medium) rs1243384421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5224202,Human_RBP_ID_8221123,Human_RBP_ID_18466772,Human_RBP_ID_26795460 92226 RMVar_ID_92226 Human_SNP_ID_368627025 m1A Human chr8 - 73878776 73878776 73878776 GGTGAGAGGAGTTTGCTGCATCTGGGCGGGCCAGGGAGCCGCCGAGAGAGTGCCAGCGTTCGGGC GGTGAGAGGAGTTTGCTGCATCTGGGCGGGCCGGGGAGCCGCCGAGAGAGTGCCAGCGTTCGGGC T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:73878628..73878798 26863196 MeRIP-seq:(Medium) rs1053548282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18426710,Human_RBP_ID_19140234 92227 RMVar_ID_92227 Human_SNP_ID_368646651 m1A Human chr8 - 73956020 73956020 73956020 GGAGAGGAGAAAACCTATGGTGGCTGTGAAGGACCTGATGCCATGTATGTCAAATTGATATCATC GGAGAGGAGAAAACCTATGGTGGCTGTGAAGGGCCTGATGCCATGTATGTCAAATTGATATCATC T C ELOC Ensembl:ENSG00000154582 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:73955976..73956088;chr8:73955951..73969668 26863196 MeRIP-seq:(Medium) rs758728102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_703878,Human_RBP_ID_959211,Human_RBP_ID_1698969,Human_RBP_ID_2057277,Human_RBP_ID_4996606,Human_RBP_ID_5154059,Human_RBP_ID_7856267,Human_RBP_ID_9405563,Human_RBP_ID_16472837,Human_RBP_ID_17666129,Human_RBP_ID_22689234,Human_RBP_ID_23216318,Human_RBP_ID_24267765,Human_RBP_ID_26359180 Human_Splice_Rec_986682,Human_Splice_Rec_986688,Human_Splice_Rec_986696,Human_Splice_Rec_986700,Human_Splice_Rec_986706,Human_Splice_Rec_986712,Human_Splice_Rec_986718,Human_Splice_Rec_986726,Human_Splice_Rec_986736,Human_Splice_Rec_986744 RMVar_hsa_circ_42679,RMVar_hsa_circ_369710,RMVar_hsa_circ_279358,RMVar_hsa_circ_252760,RMVar_hsa_circ_22742,RMVar_hsa_circ_252759 92228 RMVar_ID_92228 Human_SNP_ID_368647657 m1A Human chr8 - 73959753 73959753 73959753 AATTTCATAAGAACAAAATGGGTAAGCTAAAGATAATTAATTTTGTGTTTTAACTAGTAGAAACT AATTTCATAAGAACAAAATGGGTAAGCTAAAGTTAATTAATTTTGTGTTTTAACTAGTAGAAACT T A ELOC Ensembl:ENSG00000154582 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:73959751..73959850 26863410 MeRIP-seq:(Medium) rs993327257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_986680,Human_Splice_Rec_986686,Human_Splice_Rec_986694,Human_Splice_Rec_986704,Human_Splice_Rec_986710,Human_Splice_Rec_986716,Human_Splice_Rec_986724,Human_Splice_Rec_986734,Human_Splice_Rec_986742 RMVar_hsa_circ_42679,RMVar_hsa_circ_279358,RMVar_hsa_circ_252760,RMVar_hsa_circ_22742 92229 RMVar_ID_92229 Human_SNP_ID_368647658 m1A Human chr8 - 73959753 73959753 73959753 AATTTCATAAGAACAAAATGGGTAAGCTAAAGATAATTAATTTTGTGTTTTAACTAGTAGAAACT AATTTCATAAGAACAAAATGGGTAAGCTAAAGGTAATTAATTTTGTGTTTTAACTAGTAGAAACT T C ELOC Ensembl:ENSG00000154582 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:73959751..73959850 26863410 MeRIP-seq:(Medium) rs993327257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_986680,Human_Splice_Rec_986686,Human_Splice_Rec_986694,Human_Splice_Rec_986704,Human_Splice_Rec_986710,Human_Splice_Rec_986716,Human_Splice_Rec_986724,Human_Splice_Rec_986734,Human_Splice_Rec_986742 RMVar_hsa_circ_42679,RMVar_hsa_circ_279358,RMVar_hsa_circ_252760,RMVar_hsa_circ_22742 92230 RMVar_ID_92230 Human_SNP_ID_368648937 m1A Human chr8 + 73964587 73964587 73964587 GGAGGGAGATCACTTGAGGTCAGGAATTTGAGACCAGCCGGGCACTCCAGCCTGGGCCACACAGC GGAGGGAGATCACTTGAGGTCAGGAATTTGAGGCCAGCCGGGCACTCCAGCCTGGGCCACACAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73964584..73969618 26863196 MeRIP-seq:(Medium) rs1221322300 Functional Loss SNV dbSNP153 33..33 33 - - - 92231 RMVar_ID_92231 Human_SNP_ID_368651002 m1A Human chr8 - 73971832 73971832 73971832 TTTGGAAAGAGGTGGAAGGAGGGGCAGCAGCCAGCGAGACTGGGCCTTCTCCGGGCTGAGCGCGG TTTGGAAAGAGGTGGAAGGAGGGGCAGCAGCCGGCGAGACTGGGCCTTCTCCGGGCTGAGCGCGG T C ELOC Ensembl:ENSG00000154582 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:73971828..73971914 26863196 MeRIP-seq:(Medium) rs1036154543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9440899 92232 RMVar_ID_92232 Human_SNP_ID_368651106 m1A Human chr8 - 73972114 73972114 73972114 GGGGGCGGCCCTGGGATAGGGGCTGTGGCAGTACGCGGGGACCCGGCTGCGGTGGCTGCGGGACT GGGGGCGGCCCTGGGATAGGGGCTGTGGCAGTCCGCGGGGACCCGGCTGCGGTGGCTGCGGGACT T G ELOC Ensembl:ENSG00000154582 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:73971947..73972150 26863196 MeRIP-seq:(Medium) rs1332852846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255375,Human_RBP_ID_703882,Human_RBP_ID_796375,Human_RBP_ID_4995087,Human_RBP_ID_5328874,Human_RBP_ID_8944460,Human_RBP_ID_9338667,Human_RBP_ID_9354903,Human_RBP_ID_9440696,Human_RBP_ID_18426711,Human_RBP_ID_19140235,Human_RBP_ID_22465875,Human_RBP_ID_24267793,Human_RBP_ID_26182345,Human_RBP_ID_26772461 Human_Splice_Rec_986679,Human_Splice_Rec_986699,Human_Splice_Rec_986703,Human_Splice_Rec_986715,Human_Splice_Rec_986721,Human_Splice_Rec_986739 92233 RMVar_ID_92233 Human_SNP_ID_368651109 m1A Human chr8 + 73972123 73972123 73972123 GCCACCGCAGCCGGGTCCCCGCGTACTGCCACAGCCCCTATCCCAGGGCCGCCCCCCCACCCCCA GCCACCGCAGCCGGGTCCCCGCGTACTGCCACGGCCCCTATCCCAGGGCCGCCCCCCCACCCCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:73972011..73972236;chr8:73971989..73972248;chr8:73971904..73972200 26863196 MeRIP-seq:(Medium) rs1393250862 Functional Loss SNV dbSNP153 33..33 33 - - - 92234 RMVar_ID_92234 Human_SNP_ID_368651110 m1A Human chr8 + 73972123 73972123 73972123 GCCACCGCAGCCGGGTCCCCGCGTACTGCCACAGCCCCTATCCCAGGGCCGCCCCCCCACCCCCA GCCACCGCAGCCGGGTCCCCGCGTACTGCCACTGCCCCTATCCCAGGGCCGCCCCCCCACCCCCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:73972011..73972236;chr8:73971989..73972248;chr8:73971904..73972200 26863196 MeRIP-seq:(Medium) rs1393250862 Functional Loss SNV dbSNP153 33..33 33 - - - 92235 RMVar_ID_92235 Human_SNP_ID_368652355 m1A Human chr8 - 73976236 73976236 73976236 AGCGGCTGCGGACGCCCCAGCTGCACGAGTCCACGACTGCGAGACACGGCTTCCCACCCGACTGC AGCGGCTGCGGACGCCCCAGCTGCACGAGTCCGCGACTGCGAGACACGGCTTCCCACCCGACTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:73976166..73976400 26863196 MeRIP-seq:(Medium) rs774693342 Functional Loss SNV dbSNP153 33..33 33 - - - 92236 RMVar_ID_92236 Human_SNP_ID_368652375 m1A Human chr8 - 73976257 73976257 73976257 AACAGCATCACGCGGGTGACGAGCGGCTGCGGACGCCCCAGCTGCACGAGTCCACGACTGCGAGA AACAGCATCACGCGGGTGACGAGCGGCTGCGGCCGCCCCAGCTGCACGAGTCCACGACTGCGAGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr8:73976191..73976425;chr8:73976195..73976481;chr8:73976202..73976439;chr8:73976174..73976500;chr8:73976176..73976400 26863196 MeRIP-seq:(Medium) rs1481420468 Functional Loss SNV dbSNP153 33..33 33 - - - 92237 RMVar_ID_92237 Human_SNP_ID_368652379 m1A Human chr8 + 73976262 73976262 73976262 CAGTCGTGGACTCGTGCAGCTGGGGCGTCCGCAGCCGCTCGTCACCCGCGTGATGCTGTTTCTGG CAGTCGTGGACTCGTGCAGCTGGGGCGTCCGCCGCCGCTCGTCACCCGCGTGATGCTGTTTCTGG A C TMEM70 Ensembl:ENSG00000175606 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:73976201..73976400 26863196 MeRIP-seq:(Medium) rs1234242574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_703884,Human_RBP_ID_4995088,Human_RBP_ID_5481421,Human_RBP_ID_9338668,Human_RBP_ID_22517326 92238 RMVar_ID_92238 Human_SNP_ID_368731804 m1A Human chr8 - 74303885 74303885 74303885 GAACCTATAAGAGGGAGTTTGGACATTATCCCAAGGATAGGGGAAGGCTATTGATAGGTGTTAGG GAACCTATAAGAGGGAGTTTGGACATTATCCCGAGGATAGGGGAAGGCTATTGATAGGTGTTAGG T C JPH1 Ensembl:ENSG00000104369 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:74303883..74304057 26863196 MeRIP-seq:(Medium) rs950861619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52990 92239 RMVar_ID_92239 Human_SNP_ID_368734623 m1A Human chr8 + 74315476 74315476 74315476 GGCTGTCGGCGGCGGCTGCGGCGTCGTGGAGCACGCTGCCATTGCTCTGCTCGCTGCGCAGCGAG GGCTGTCGGCGGCGGCTGCGGCGTCGTGGAGCTCGCTGCCATTGCTCTGCTCGCTGCGCAGCGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:74315428..74315642 26863196 MeRIP-seq:(Medium) rs1563424927 Functional Loss SNV dbSNP153 33..33 33 - - - 92240 RMVar_ID_92240 Human_SNP_ID_368734634 m1A Human chr8 - 74315498 74315498 74315498 CACCGCTGCGTACCTCGCTGGCCTCGCTGCGCAGCGAGCAGAGCAATGGCAGCGTGCTCCACGAC CACCGCTGCGTACCTCGCTGGCCTCGCTGCGCGGCGAGCAGAGCAATGGCAGCGTGCTCCACGAC T C JPH1 Ensembl:ENSG00000104369 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:74315376..74315550 26863196 MeRIP-seq:(Medium) rs753904915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328683,RMVar_hsa_circ_52990,RMVar_hsa_circ_252763 92241 RMVar_ID_92241 Human_SNP_ID_368736089 m1A Human chr8 - 74321462 74321462 74321462 AGGAGGAGGAGGAAGGCGGCGGTGGCGGCGGCAAAAGAGGAGGGAGGACGGGGGCGGCGTCGGAC AGGAGGAGGAGGAAGGCGGCGGTGGCGGCGGCCAAAGAGGAGGGAGGACGGGGGCGGCGTCGGAC T G JPH1 Ensembl:ENSG00000104369 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:74320926..74321550 26863196 MeRIP-seq:(Medium) rs1169379860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5002565 92242 RMVar_ID_92242 Human_SNP_ID_368742631 m1A Human chr8 + 74350471 74350471 74350471 CACCCGTGCTCGCGCACCCCAAGATGGCTGAGAGGCAGGAAGAGCAGAGAGGGAGCCCGCCCTTG CACCCGTGCTCGCGCACCCCAAGATGGCTGAGGGGCAGGAAGAGCAGAGAGGGAGCCCGCCCTTG A G GDAP1 Ensembl:ENSG00000104381 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:74350420..74350546;chr8:74350423..74350538 26863196 MeRIP-seq:(Medium) rs757057386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18426852 92243 RMVar_ID_92243 Human_SNP_ID_368742634 m1A Human chr8 + 74350484 74350484 74350484 GCACCCCAAGATGGCTGAGAGGCAGGAAGAGCAGAGAGGGAGCCCGCCCTTGAGGGCGGAAGGCA GCACCCCAAGATGGCTGAGAGGCAGGAAGAGCGGAGAGGGAGCCCGCCCTTGAGGGCGGAAGGCA A G GDAP1 Ensembl:ENSG00000104381 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:74350434..74350537 26863196 MeRIP-seq:(Medium) rs879253884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18426852 Human_Splice_Rec_986843,Human_Splice_Rec_986861,Human_Splice_Rec_986863,Human_Splice_Rec_986871 92244 RMVar_ID_92244 Human_SNP_ID_368746492 m1A Human chr8 - 74365539 74365539 74365539 CACCAGAAATGGCTTCTAAGGCCTTCATGGCCAGCTCCAGGGAAACTGTCTTCCTGTCACCATGA CACCAGAAATGGCTTCTAAGGCCTTCATGGCCTGCTCCAGGGAAACTGTCTTCCTGTCACCATGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:74365492..74365622 26863196 MeRIP-seq:(Medium) rs1314670545 Functional Loss SNV dbSNP153 33..33 33 - - - 92245 RMVar_ID_92245 Human_SNP_ID_275759356 m1A Human chr6 - 46652683 46652683 46652683 TACGAAGGAGAGCTGCAAAAGTTGCAGCAGAAAGGTTGGGAGTCCCGACAGGTTCCGTAGCCCAC TACGAAGGAGAGCTGCAAAAGTTGCAGCAGAAGGGTTGGGAGTCCCGACAGGTTCCGTAGCCCAC T C CYP39A1 Ensembl:ENSG00000146233 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:46652632..46652741 26863196 MeRIP-seq:(Medium) rs555227266 Functional Loss SNV dbSNP153 33..33 33 - - - 92246 RMVar_ID_92246 Human_SNP_ID_275759470 m1A Human chr6 + 46653048 46653048 46653048 CCAGCTGGGACTGCTAGGAAGGTTGCGGGTCCACCCGGCCGAGCCGAACGAGGGAAATGGTCCTC CCAGCTGGGACTGCTAGGAAGGTTGCGGGTCCTCCCGGCCGAGCCGAACGAGGGAAATGGTCCTC A T SLC25A27 Ensembl:ENSG00000153291 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:46653002..46653218 26863196 MeRIP-seq:(Medium) rs1305252271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21349424 92247 RMVar_ID_92247 Human_SNP_ID_275759583 m1A Human chr6 + 46653264 46653264 46653264 ACCCAGAGATGGCCCCGAGCGAGCAAATTCCTACTGTCCGGCTGCGCGGCTACCGTGGCCGAGCT ACCCAGAGATGGCCCCGAGCGAGCAAATTCCTGCTGTCCGGCTGCGCGGCTACCGTGGCCGAGCT A G SLC25A27 Ensembl:ENSG00000153291 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:46653219..46653360 26863196 MeRIP-seq:(Medium) rs780332313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252328,Human_RBP_ID_4892916 Human_Splice_Rec_775637,Human_Splice_Rec_775649 92248 RMVar_ID_92248 Human_SNP_ID_275759628 m1A Human chr6 + 46653339 46653339 46653339 CTGCCCACGCCTGGGCCTCCCGGGCCAGTGGCACGCGCCGCGCTGGGGGAGGGTGCGCGGGCGGC CTGCCCACGCCTGGGCCTCCCGGGCCAGTGGCCCGCGCCGCGCTGGGGGAGGGTGCGCGGGCGGC A C SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:46653294..46653398 26863196 MeRIP-seq:(Medium) rs748424637 Functional Loss SNV dbSNP153 33..33 33 - - - 92249 RMVar_ID_92249 Human_SNP_ID_275929745 m1A Human chr6 + 47309531 47309531 47309531 GAGAGGTCCCCATGGCTGAACCGGGGACTCGCAGGGGCGCCCGGGGCGCGCGGGGCAGCTGGAAT GAGAGGTCCCCATGGCTGAACCGGGGACTCGCCGGGGCGCCCGGGGCGCGCGGGGCAGCTGGAAT A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:47309486..47309870 26863196 MeRIP-seq:(Medium) rs1459568412 Functional Loss SNV dbSNP153 33..33 33 - - - 92250 RMVar_ID_92250 Human_SNP_ID_275994021 m1A Human chr6 + 47567901 47567901 47567901 ATTGTTTTTCAGATAAATTGGTGGCAGTATGGAGAGTGAATTGCAATGTGGGGAGTAGATTGGAG ATTGTTTTTCAGATAAATTGGTGGCAGTATGGCGAGTGAATTGCAATGTGGGGAGTAGATTGGAG A C CD2AP Ensembl:ENSG00000198087 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:47567801..47567969 26863196 MeRIP-seq:(Medium) rs79378395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52595,RMVar_hsa_circ_3198,RMVar_hsa_circ_354153,RMVar_hsa_circ_108122,RMVar_hsa_circ_109092,RMVar_hsa_circ_79850,RMVar_hsa_circ_64125,RMVar_hsa_circ_238868,RMVar_hsa_circ_238869,RMVar_hsa_circ_316637,RMVar_hsa_circ_360889,RMVar_hsa_circ_238867,RMVar_hsa_circ_367533,RMVar_hsa_circ_60093,RMVar_hsa_circ_62012,RMVar_hsa_circ_238874,RMVar_hsa_circ_62273,RMVar_hsa_circ_45963,RMVar_hsa_circ_66158,RMVar_hsa_circ_350211,RMVar_hsa_circ_350848,RMVar_hsa_circ_361817,RMVar_hsa_circ_349688,RMVar_hsa_circ_58671,RMVar_hsa_circ_238875 92251 RMVar_ID_92251 Human_SNP_ID_276503341 m1A Human chr6 + 49463189 49463189 49463189 CCCCGCCTCACCTGTCAGACATCCACACAGCCAGGCCTCCCCGCCCTCACCAAGCCCACACAAAC CCCCGCCTCACCTGTCAGACATCCACACAGCCGGGCCTCCCCGCCCTCACCAAGCCCACACAAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:49463073..49463280;chr6:49459476..49463285 26863196 MeRIP-seq:(Medium) rs1369538484 Functional Loss SNV dbSNP153 33..33 33 - - - 92252 RMVar_ID_92252 Human_SNP_ID_277153686 m1A Human chr6 - 52016025 52016025 52016025 GTCAGTAGGTCCTGGCTCCATTGAATTCAGGGACTTCATCTGAATCCCCAAAACTCTTCTTTGGG GTCAGTAGGTCCTGGCTCCATTGAATTCAGGGGCTTCATCTGAATCCCCAAAACTCTTCTTTGGG T C PKHD1 Ensembl:ENSG00000170927 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:52016019..52016103 26863410 MeRIP-seq:(Medium) rs931365768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54417,RMVar_hsa_circ_55932,RMVar_hsa_circ_70075,RMVar_hsa_circ_70953,RMVar_hsa_circ_68894,RMVar_hsa_circ_356941,RMVar_hsa_circ_65821,RMVar_hsa_circ_364727,RMVar_hsa_circ_360248,RMVar_hsa_circ_72664,RMVar_hsa_circ_73777,RMVar_hsa_circ_58833,RMVar_hsa_circ_360460,RMVar_hsa_circ_62010,RMVar_hsa_circ_54259,RMVar_hsa_circ_238902,RMVar_hsa_circ_115901,RMVar_hsa_circ_359777,RMVar_hsa_circ_350934,RMVar_hsa_circ_357925,RMVar_hsa_circ_77728,RMVar_hsa_circ_110694,RMVar_hsa_circ_351946,RMVar_hsa_circ_369201,RMVar_hsa_circ_120068,RMVar_hsa_circ_87952,RMVar_hsa_circ_238904,RMVar_hsa_circ_238906,RMVar_hsa_circ_24874,RMVar_hsa_circ_238905,RMVar_hsa_circ_238903 92253 RMVar_ID_92253 Human_SNP_ID_277215540 m1A Human chr6 - 52264159 52264159 52264159 TAGGCTTTGGGTGGTTCCAATTGGTGGAGAGAAGCTCTGAGGCACGTCATGCAGGTCAAGAAAGC TAGGCTTTGGGTGGTTCCAATTGGTGGAGAGACGCTCTGAGGCACGTCATGCAGGTCAAGAAAGC T G MCM3 Ensembl:ENSG00000112118 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:52264077..52264228 26863196 MeRIP-seq:(Medium) rs1412717826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_666048,Human_RBP_ID_789781,Human_RBP_ID_1674555,Human_RBP_ID_2023083,Human_RBP_ID_3811497,Human_RBP_ID_4914712,Human_RBP_ID_5122035,Human_RBP_ID_5219200,Human_RBP_ID_5533090,Human_RBP_ID_7614463,Human_RBP_ID_9354716,Human_RBP_ID_9400709,Human_RBP_ID_15846199,Human_RBP_ID_17307493,Human_RBP_ID_18078229,Human_RBP_ID_18450545,Human_RBP_ID_18867366,Human_RBP_ID_22313669,Human_RBP_ID_22832011,Human_RBP_ID_23062943,Human_RBP_ID_23214866,Human_RBP_ID_24166254,Human_RBP_ID_24437235,Human_RBP_ID_26039274,Human_RBP_ID_26354121,Human_RBP_ID_27099356,Human_RBP_ID_27348143 Human_miRNA_ID_3116832 RMVar_hsa_circ_238913,RMVar_hsa_circ_83669,RMVar_hsa_circ_99793,RMVar_hsa_circ_121340,RMVar_hsa_circ_121805,RMVar_hsa_circ_113495,RMVar_hsa_circ_89985,RMVar_hsa_circ_99124,RMVar_hsa_circ_89607,RMVar_hsa_circ_79221,RMVar_hsa_circ_79823,RMVar_hsa_circ_238915,RMVar_hsa_circ_238917,RMVar_hsa_circ_78156,RMVar_hsa_circ_238916,RMVar_hsa_circ_238914,RMVar_hsa_circ_238909,RMVar_hsa_circ_238911,RMVar_hsa_circ_238912,RMVar_hsa_circ_238910,RMVar_hsa_circ_238907,RMVar_hsa_circ_238908 92254 RMVar_ID_92254 Human_SNP_ID_277216671 m1A Human chr6 - 52267955 52267953 52267956 ACACTTGCCTTGGTCTTAGGTTCTGGAGAAGGAGAAGAAACGTAAGAAGCGAAGTGAGGATGAAT ACACTTGCCTTGGTCTTAGGTTCTGGAGAAG___AAGAAACGTAAGAAGCGAAGTGAGGATGAAT TCTC T MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:52267876..52267975 26863196 MeRIP-seq:(Medium) rs769676124 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_79471,Human_RBP_ID_1678510,Human_RBP_ID_2023106,Human_RBP_ID_3010510,Human_RBP_ID_7614506,Human_RBP_ID_8270200,Human_RBP_ID_8646738,Human_RBP_ID_9400726,Human_RBP_ID_15846330,Human_RBP_ID_19131380,Human_RBP_ID_22683006,Human_RBP_ID_23067593,Human_RBP_ID_24548421,Human_RBP_ID_26354128,Human_RBP_ID_27827773 Human_Splice_Rec_777316,Human_Splice_Rec_777317,Human_Splice_Rec_777346,Human_Splice_Rec_777347,Human_Splice_Rec_777378,Human_Splice_Rec_777379,Human_Splice_Rec_777408,Human_Splice_Rec_777409,Human_Splice_Rec_777422,Human_Splice_Rec_777423 RMVar_hsa_circ_5805,RMVar_hsa_circ_238913,RMVar_hsa_circ_83669,RMVar_hsa_circ_121340,RMVar_hsa_circ_121805,RMVar_hsa_circ_113495,RMVar_hsa_circ_89985,RMVar_hsa_circ_99124,RMVar_hsa_circ_89607,RMVar_hsa_circ_79221,RMVar_hsa_circ_79823,RMVar_hsa_circ_238915,RMVar_hsa_circ_78156,RMVar_hsa_circ_238916,RMVar_hsa_circ_238914,RMVar_hsa_circ_238909,RMVar_hsa_circ_238911,RMVar_hsa_circ_238912,RMVar_hsa_circ_238910,RMVar_hsa_circ_238907,RMVar_hsa_circ_238908,RMVar_hsa_circ_335585,RMVar_hsa_circ_110326,RMVar_hsa_circ_110458,RMVar_hsa_circ_6089,RMVar_hsa_circ_115005,RMVar_hsa_circ_238919,RMVar_hsa_circ_238920,RMVar_hsa_circ_108765,RMVar_hsa_circ_238921,RMVar_hsa_circ_238922,RMVar_hsa_circ_238923,RMVar_hsa_circ_280485,RMVar_hsa_circ_339495,RMVar_hsa_circ_353656,RMVar_hsa_circ_281477,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924,RMVar_hsa_circ_238926,RMVar_hsa_circ_238927,RMVar_hsa_circ_238925 92255 RMVar_ID_92255 Human_SNP_ID_277216973 m1A Human chr6 + 52269170 52269170 52269170 AGGTCCACAGTCTTGCTCATGCGGGCCTTCGCATGGGCTGTGGCCAGTCGAATCAGAGTTTCCAG AGGTCCACAGTCTTGCTCATGCGGGCCTTCGCGTGGGCTGTGGCCAGTCGAATCAGAGTTTCCAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52269076..52269250 32194978 MeRIP-seq:(Medium) rs1182190239 Functional Loss SNV dbSNP153 33..33 33 - - - 92256 RMVar_ID_92256 Human_SNP_ID_277217846 m1A Human chr6 - 52272379 52272379 52272379 CATGTGGCCAAAATCATCAAGCCTGTCCTGACACAGGAGTCGGCCACCTACATTGCAGAAGAGTA CATGTGGCCAAAATCATCAAGCCTGTCCTGACGCAGGAGTCGGCCACCTACATTGCAGAAGAGTA T C MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:52272261..52272401 26863196 MeRIP-seq:(Medium) rs762153505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951415,Human_RBP_ID_2023133,Human_RBP_ID_3811527,Human_RBP_ID_4893457,Human_RBP_ID_7614550,Human_RBP_ID_9400730,Human_RBP_ID_15846565,Human_RBP_ID_18195615,Human_RBP_ID_18867410,Human_RBP_ID_26353227,Human_RBP_ID_26828592 Human_Splice_Rec_777312,Human_Splice_Rec_777313,Human_Splice_Rec_777342,Human_Splice_Rec_777343,Human_Splice_Rec_777374,Human_Splice_Rec_777375,Human_Splice_Rec_777404,Human_Splice_Rec_777405,Human_Splice_Rec_777418,Human_Splice_Rec_777419 RMVar_hsa_circ_5805,RMVar_hsa_circ_238913,RMVar_hsa_circ_121340,RMVar_hsa_circ_121805,RMVar_hsa_circ_113495,RMVar_hsa_circ_89985,RMVar_hsa_circ_99124,RMVar_hsa_circ_89607,RMVar_hsa_circ_79823,RMVar_hsa_circ_78156,RMVar_hsa_circ_238914,RMVar_hsa_circ_238909,RMVar_hsa_circ_238911,RMVar_hsa_circ_238912,RMVar_hsa_circ_238910,RMVar_hsa_circ_238907,RMVar_hsa_circ_238908,RMVar_hsa_circ_335585,RMVar_hsa_circ_110458,RMVar_hsa_circ_6089,RMVar_hsa_circ_115005,RMVar_hsa_circ_238920,RMVar_hsa_circ_108765,RMVar_hsa_circ_238921,RMVar_hsa_circ_238922,RMVar_hsa_circ_238923,RMVar_hsa_circ_339495,RMVar_hsa_circ_353656,RMVar_hsa_circ_281477,RMVar_hsa_circ_116391,RMVar_hsa_circ_3283,RMVar_hsa_circ_56281,RMVar_hsa_circ_238924,RMVar_hsa_circ_238926,RMVar_hsa_circ_238925,RMVar_hsa_circ_125321,RMVar_hsa_circ_238928,RMVar_hsa_circ_36316,RMVar_hsa_circ_295603,RMVar_hsa_circ_373749,RMVar_hsa_circ_80271,RMVar_hsa_circ_238929,RMVar_hsa_circ_238930,RMVar_hsa_circ_238931 92257 RMVar_ID_92257 Human_SNP_ID_277220549 m1A Human chr6 + 52282126 52282126 52282126 TCAGAATAACGTCGCTCTATGGTCTTCTTAGTAGCAGGACAGTAGTGGACACTGCGGACGACTTT TCAGAATAACGTCGCTCTATGGTCTTCTTAGTGGCAGGACAGTAGTGGACACTGCGGACGACTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52282076..52282200 32194978 MeRIP-seq:(Medium) rs768941914 Functional Loss SNV dbSNP153 33..33 33 - - - 92258 RMVar_ID_92258 Human_SNP_ID_277220720 m1A Human chr6 - 52282689 52282689 52282689 TCTCCCCGCGGACTCTTACCTCCTGCTTCCTCAGCTGTGTGGTCTGTGTGGAGGGCATTGTCACT TCTCCCCGCGGACTCTTACCTCCTGCTTCCTCTGCTGTGTGGTCTGTGTGGAGGGCATTGTCACT T A MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52282651..52282875 32194978 MeRIP-seq:(Medium) rs758234731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1674751,Human_RBP_ID_2023226,Human_RBP_ID_3811567,Human_RBP_ID_7614692,Human_RBP_ID_8902147,Human_RBP_ID_15847078,Human_RBP_ID_17307507,Human_RBP_ID_18078273,Human_RBP_ID_18867504,Human_RBP_ID_19018794,Human_RBP_ID_22832058,Human_RBP_ID_24166376,Human_RBP_ID_27525407 Human_Splice_Rec_777295,Human_Splice_Rec_777325,Human_Splice_Rec_777357,Human_Splice_Rec_777387 RMVar_hsa_circ_79823,RMVar_hsa_circ_78156,RMVar_hsa_circ_238907,RMVar_hsa_circ_238908,RMVar_hsa_circ_110458,RMVar_hsa_circ_238923,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924,RMVar_hsa_circ_238925,RMVar_hsa_circ_125321,RMVar_hsa_circ_238928,RMVar_hsa_circ_6182,RMVar_hsa_circ_6725,RMVar_hsa_circ_370568,RMVar_hsa_circ_24461,RMVar_hsa_circ_238938,RMVar_hsa_circ_354042 92259 RMVar_ID_92259 Human_SNP_ID_277221432 m1A Human chr6 + 52284690 52284690 52284690 ACCACGGTACCCGCCATGCCCGCTGCCAAAGAACTACCTCCACCAAAGTCGCGTGGAGGTTCCCA ACCACGGTACCCGCCATGCCCGCTGCCAAAGACCTACCTCCACCAAAGTCGCGTGGAGGTTCCCA A C NONHSAG043930.2 RNACentral:URS00008B5BEC lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:52284566..52284750 26863196 MeRIP-seq:(Medium) rs915669790 Functional Loss SNV dbSNP153 33..33 33 - - - 92260 RMVar_ID_92260 Human_SNP_ID_277221444 m1A Human chr6 - 52284706 52284706 52284706 CGGGGTGGAGTCATCCTGGGAACCTCCACGCGACTTTGGTGGAGGTAGTTCTTTGGCAGCGGGCA CGGGGTGGAGTCATCCTGGGAACCTCCACGCGGCTTTGGTGGAGGTAGTTCTTTGGCAGCGGGCA T C MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:52283301..52284775;chr6:52284543..52284775 26863196 MeRIP-seq:(Medium) rs761088358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1327977,Human_RBP_ID_1395811,Human_RBP_ID_4893541,Human_RBP_ID_8905848,Human_RBP_ID_18078280 RMVar_hsa_circ_78156,RMVar_hsa_circ_238907,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924 92261 RMVar_ID_92261 Human_SNP_ID_277221445 m1A Human chr6 - 52284706 52284706 52284706 CGGGGTGGAGTCATCCTGGGAACCTCCACGCGACTTTGGTGGAGGTAGTTCTTTGGCAGCGGGCA CGGGGTGGAGTCATCCTGGGAACCTCCACGCGCCTTTGGTGGAGGTAGTTCTTTGGCAGCGGGCA T G MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:52283301..52284775;chr6:52284543..52284775 26863196 MeRIP-seq:(Medium) rs761088358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1327977,Human_RBP_ID_1395811,Human_RBP_ID_4893541,Human_RBP_ID_8905848,Human_RBP_ID_18078280 RMVar_hsa_circ_78156,RMVar_hsa_circ_238907,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924 92262 RMVar_ID_92262 Human_SNP_ID_277239853 m1A Human chr6 + 52362181 52362181 52362181 TCACAGCCACCCGCGGGAAGCTCGTGGCCGGGACCCCGAGGCGGGAGCGCGGGCTGGGCCGGGCT TCACAGCCACCCGCGGGAAGCTCGTGGCCGGGGCCCCGAGGCGGGAGCGCGGGCTGGGCCGGGCT A G PAQR8,EFHC1 Ensembl:ENSG00000170915,Ensembl:ENSG00000096093 Protein coding,Protein coding intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:52362149..52362406 26863196 MeRIP-seq:(Medium) rs894784035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840255,Human_RBP_ID_3821271,Human_RBP_ID_4903396,Human_RBP_ID_5242760,Human_RBP_ID_18425668,Human_RBP_ID_23120373 Human_Splice_Rec_777441,Human_Splice_Rec_777447,Human_Splice_Rec_777465,Human_Splice_Rec_777483,Human_Splice_Rec_777503 92263 RMVar_ID_92263 Human_SNP_ID_277239860 m1A Human chr6 - 52362203 52362203 52362203 GCCGAGCCCGTGCGCGTAGCCCAGCCCGGCCCAGCCCGCGCTCCCGCCTCGGGGTCCCGGCCACG GCCGAGCCCGTGCGCGTAGCCCAGCCCGGCCCGGCCCGCGCTCCCGCCTCGGGGTCCCGGCCACG T C lnc-MCM3-3,lnc-MCM3-3:2 RNACentral:URS0000D59D71,RNACentral:URS0000D5DF87 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:52362167..52363008;chr6:52362195..52362331 26863196 MeRIP-seq:(Medium) rs1454866578 Functional Loss SNV dbSNP153 33..33 33 - - - 92264 RMVar_ID_92264 Human_SNP_ID_277271740 m1A Human chr6 + 52499636 52499634 52499636 AAAAAGAAGGGGTACTGACAAAGGAGGTCCCAAAAGAGACCCCAGAAGCACACACCCACCCCAAG AAAAAGAAGGGGTACTGACAAAGGAGGTCCC__AAGAGACCCCAGAAGCACACACCCACCCCAAG CAA C EFHC1 Ensembl:ENSG00000096093 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52499587..52499688 32194978 MeRIP-seq:(Medium) rs112044263 Functional Loss DEL dbSNP153 32..33 33 - - - 92265 RMVar_ID_92265 Human_SNP_ID_277272786 m1A Human chr6 - 52502990 52502990 52502990 TATTCTTCCACAAACCATTCTCAATAAAGCCAAAAATCTTTCTCTTTCTCCCCCTCAGGCCACCT TATTCTTCCACAAACCATTCTCAATAAAGCCAGAAATCTTTCTCTTTCTCCCCCTCAGGCCACCT T C TRAM2 Ensembl:ENSG00000065308 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:52502939..52503040 26863196 MeRIP-seq:(Medium) rs144061637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3811649,Human_RBP_ID_5152696,Human_RBP_ID_17309626,Human_RBP_ID_17536502,Human_RBP_ID_21387232 Human_miRNA_ID_186320 92266 RMVar_ID_92266 Human_SNP_ID_277290392 m1A Human chr6 + 52576949 52576949 52576949 GCAGCGGGCGCGCAGCGGCCGGCGGGGCCCGCACCCTGCGCTCACGAACCGCAGCGCAAACTTCT GCAGCGGGCGCGCAGCGGCCGGCGGGGCCCGCGCCCTGCGCTCACGAACCGCAGCGCAAACTTCT A G TRAM2-AS1 Ensembl:ENSG00000225791 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:52576906..52577040 26863196 MeRIP-seq:(Medium) rs1181653225 Functional Loss SNV dbSNP153 33..33 33 - - - 92267 RMVar_ID_92267 Human_SNP_ID_277290548 m1A Human chr6 - 52577267 52577267 52577267 GAGAATGCGGCCGGGCGCGGCGCTGGCGCGGGACGAGGAGGAGCCGAGCCCCGCTCGCCGCCCCC GAGAATGCGGCCGGGCGCGGCGCTGGCGCGGGTCGAGGAGGAGCCGAGCCCCGCTCGCCGCCCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:52577224..52577366 26863196 MeRIP-seq:(Medium) rs1290466405 Functional Loss SNV dbSNP153 33..33 33 - - - 92268 RMVar_ID_92268 Human_SNP_ID_277311233 m1A Human chr6 - 52664500 52664500 52664500 GTATGGGTTCTCGGTGGCGCCCGTAGTCCCCAAGACCTTCTTCCTCTAACTTGCTTCTAACACAC GTATGGGTTCTCGGTGGCGCCCGTAGTCCCCAGGACCTTCTTCCTCTAACTTGCTTCTAACACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:52664449..52664699 26863196 MeRIP-seq:(Medium) rs1448520913 Functional Loss SNV dbSNP153 33..33 33 - - - 92269 RMVar_ID_92269 Human_SNP_ID_277400448 m1A Human chr6 - 52995884 52995884 52995884 TTGGATGTGTCTGGAGTCTTGGAAGCTTGACTACCCTACGTTCTCCTACAAATGGACCTTGAGAG TTGGATGTGTCTGGAGTCTTGGAAGCTTGACTGCCCTACGTTCTCCTACAAATGGACCTTGAGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52995826..52995925 32194978 MeRIP-seq:(Medium) rs934625113 Functional Loss SNV dbSNP153 33..33 33 - - - 92270 RMVar_ID_92270 Human_SNP_ID_277400450 m1A Human chr6 - 52995887 52995887 52995887 CATTTGGATGTGTCTGGAGTCTTGGAAGCTTGACTACCCTACGTTCTCCTACAAATGGACCTTGA CATTTGGATGTGTCTGGAGTCTTGGAAGCTTGGCTACCCTACGTTCTCCTACAAATGGACCTTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr6:52995829..52995914;chr6:52995767..52995906;chr6:52995627..52995931;chr6:52995768..52995902 26863196 MeRIP-seq:(Medium) rs974610349 Functional Loss SNV dbSNP153 33..33 33 - - - 92271 RMVar_ID_92271 Human_SNP_ID_277403745 m1A Human chr6 - 53009877 53009877 53009877 GGGATGGAGAAGAAACTGAAAAGGTGACTGAAAGGAAGTAGTCTGTGAAGGGGAAGAACAGCATG GGGATGGAGAAGAAACTGAAAAGGTGACTGAAGGGAAGTAGTCTGTGAAGGGGAAGAACAGCATG T C CILK1 Ensembl:ENSG00000112144 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:53009840..53010021 26863196 MeRIP-seq:(Medium) rs1441370656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76952,RMVar_hsa_circ_369747,RMVar_hsa_circ_238969,RMVar_hsa_circ_238970 92272 RMVar_ID_92272 Human_SNP_ID_277407219 m1A Human chr6 - 53025282 53025282 53025282 CAGAGGGAGTTGCCATAGTGGGTAGGGGCTGCAGAACAAAGGACCCATTATAACGGAACTGCCAC CAGAGGGAGTTGCCATAGTGGGTAGGGGCTGCGGAACAAAGGACCCATTATAACGGAACTGCCAC T C CILK1 Ensembl:ENSG00000112144 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:53025260..53025426 26863196 MeRIP-seq:(Medium) rs1249682821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73379,RMVar_hsa_circ_70641,RMVar_hsa_circ_238971,RMVar_hsa_circ_84314,RMVar_hsa_circ_343499 92273 RMVar_ID_92273 Human_SNP_ID_277415130 m1A Human chr6 - 53061628 53061628 53061628 CGCCCCGCTCGTCGAGGAGCTGCGCTCACCTCAGGGGCGGGCCCCCGCCTGCGTTCGCGGCGCCA CGCCCCGCTCGTCGAGGAGCTGCGCTCACCTCTGGGGCGGGCCCCCGCCTGCGTTCGCGGCGCCA T A CILK1 Ensembl:ENSG00000112144 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:53061598..53061775 26863196 MeRIP-seq:(Medium) rs1211647973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904968 Human_Splice_Rec_778307,Human_Splice_Rec_778331 92274 RMVar_ID_92274 Human_SNP_ID_277415132 m1A Human chr6 - 53061633 53061633 53061633 GGCTGCGCCCCGCTCGTCGAGGAGCTGCGCTCACCTCAGGGGCGGGCCCCCGCCTGCGTTCGCGG GGCTGCGCCCCGCTCGTCGAGGAGCTGCGCTCCCCTCAGGGGCGGGCCCCCGCCTGCGTTCGCGG T G CILK1 Ensembl:ENSG00000112144 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:53061604..53061713 26863196 MeRIP-seq:(Medium) rs953203679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904968 Human_Splice_Rec_778307,Human_Splice_Rec_778331 92275 RMVar_ID_92275 Human_SNP_ID_277416104 m1A Human chr6 - 53065474 53065474 53065474 GGGGATTGTGCGAGCACCGGAGCGTCAGCCCTACTGGAGACCCCGGACGCCGCCGCGGAGCTGCC GGGGATTGTGCGAGCACCGGAGCGTCAGCCCTGCTGGAGACCCCGGACGCCGCCGCGGAGCTGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:53065426..53065750 26863196 MeRIP-seq:(Medium) rs1021936036 Functional Loss SNV dbSNP153 33..33 33 - - - 92276 RMVar_ID_92276 Human_SNP_ID_277472244 m1A Human chr6 - 53295701 53295701 53295701 ATCAGTATCTTTTTTTTTCTTAATAGGTTTTCAAATGGAACATTTTGATGCATCACTTAGTACCT ATCAGTATCTTTTTTTTTCTTAATAGGTTTTCCAATGGAACATTTTGATGCATCACTTAGTACCT T G ELOVL5 Ensembl:ENSG00000012660 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:53295651..53295765 26863196 MeRIP-seq:(Medium) rs1372398655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78865,Human_RBP_ID_2023450,Human_RBP_ID_4894046 Human_Splice_Rec_778488,Human_Splice_Rec_778489,Human_Splice_Rec_778504,Human_Splice_Rec_778505,Human_Splice_Rec_778516,Human_Splice_Rec_778517,Human_Splice_Rec_778530,Human_Splice_Rec_778531,Human_Splice_Rec_778540,Human_Splice_Rec_778541,Human_Splice_Rec_778550,Human_Splice_Rec_778551,Human_Splice_Rec_778562,Human_Splice_Rec_778563 RMVar_hsa_circ_106233,RMVar_hsa_circ_104715,RMVar_hsa_circ_238984,RMVar_hsa_circ_238985,RMVar_hsa_circ_238992,RMVar_hsa_circ_238997,RMVar_hsa_circ_370444,RMVar_hsa_circ_47010,RMVar_hsa_circ_332334 92277 RMVar_ID_92277 Human_SNP_ID_277485349 m1A Human chr6 + 53347971 53347971 53347971 GGCGTGGAAACAGTAAAAAGGCACTTTTCCTTACAACTCGCAAGACAACACACACTCTAGCTCCC GGCGTGGAAACAGTAAAAAGGCACTTTTCCTTTCAACTCGCAAGACAACACACACTCTAGCTCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:53347966..53348146 26863196 MeRIP-seq:(Medium) rs1327620454 Functional Loss SNV dbSNP153 33..33 33 - - - 92278 RMVar_ID_92278 Human_SNP_ID_277485777 m1A Human chr6 + 53348905 53348905 53348905 GGGAGCGCGGGTGGCAGCCGGCGCAGAGGCGGATGTAGAAGGAGACACCGGTGGCTAGGACCCGC GGGAGCGCGGGTGGCAGCCGGCGCAGAGGCGGCTGTAGAAGGAGACACCGGTGGCTAGGACCCGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:53348734..53348975;chr6:53348771..53348975;chr6:53348729..53348950 26863196 MeRIP-seq:(Medium) rs767448086 Functional Loss SNV dbSNP153 33..33 33 - - - 92279 RMVar_ID_92279 Human_SNP_ID_277485778 m1A Human chr6 + 53348905 53348905 53348905 GGGAGCGCGGGTGGCAGCCGGCGCAGAGGCGGATGTAGAAGGAGACACCGGTGGCTAGGACCCGC GGGAGCGCGGGTGGCAGCCGGCGCAGAGGCGGTTGTAGAAGGAGACACCGGTGGCTAGGACCCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:53348734..53348975;chr6:53348771..53348975;chr6:53348729..53348950 26863196 MeRIP-seq:(Medium) rs767448086 Functional Loss SNV dbSNP153 33..33 33 - - - 92280 RMVar_ID_92280 Human_SNP_ID_277485783 m1A Human chr6 - 53348908 53348908 53348908 CGCGCGGGTCCTAGCCACCGGTGTCTCCTTCTACATCCGCCTCTGCGCCGGCTGCCACCCGCGCT CGCGCGGGTCCTAGCCACCGGTGTCTCCTTCTGCATCCGCCTCTGCGCCGGCTGCCACCCGCGCT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:53348783..53348950 26863196 MeRIP-seq:(Medium) rs1419553601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169008,Human_RBP_ID_251084,Human_RBP_ID_666429,Human_RBP_ID_4903406,Human_RBP_ID_5511876,Human_RBP_ID_9336212,Human_RBP_ID_17421788,Human_RBP_ID_22461352,Human_RBP_ID_22534115,Human_RBP_ID_27099583 Human_Splice_Rec_778487,Human_Splice_Rec_778503,Human_Splice_Rec_778515,Human_Splice_Rec_778529,Human_Splice_Rec_778539,Human_Splice_Rec_778549,Human_Splice_Rec_778561 Human_miRNA_ID_2272007 RMVar_hsa_circ_104715,RMVar_hsa_circ_238984 92281 RMVar_ID_92281 Human_SNP_ID_277529399 m1A Human chr6 - 53519201 53519201 53519201 GTAAAGGGAAGCTGGCAGGTAATTGGCAGGCCAGGTCAGGTTAACCATAAATTTTAGTTGTTCTC GTAAAGGGAAGCTGGCAGGTAATTGGCAGGCCGGGTCAGGTTAACCATAAATTTTAGTTGTTCTC T C GCLC Ensembl:ENSG00000001084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:53519172..53519376 26863196 MeRIP-seq:(Medium) rs1163030210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239000,RMVar_hsa_circ_351776,RMVar_hsa_circ_368645,RMVar_hsa_circ_55917,RMVar_hsa_circ_350029,RMVar_hsa_circ_355534 92282 RMVar_ID_92282 Human_SNP_ID_277560906 m1A Human chr6 + 53651794 53651794 53651794 TGTACTTCTTCTCGCCCTCGTTCCAGCCCCCCACCAGGTAGGCGCGGCCATGCAGCGCCGAGACG TGTACTTCTTCTCGCCCTCGTTCCAGCCCCCCGCCAGGTAGGCGCGGCCATGCAGCGCCGAGACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:53651755..53651855 26863196 MeRIP-seq:(Medium) rs767600623 Functional Loss SNV dbSNP153 33..33 33 - - - 92283 RMVar_ID_92283 Human_SNP_ID_277599439 m1A Human chr6 - 53813064 53813064 53813064 CTCTCTCTGTACAGCATCCCAAGTACCTTTTCATCGGCATCCTCAGTGGCCCCATCCCACCCTCT CTCTCTCTGTACAGCATCCCAAGTACCTTTTCCTCGGCATCCTCAGTGGCCCCATCCCACCCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:53813043..53813137;chr6:53813027..53813111 26863196 MeRIP-seq:(Medium) rs576507226 Functional Loss SNV dbSNP153 33..33 33 - - - 92284 RMVar_ID_92284 Human_SNP_ID_277613506 m1A Human chr6 + 53873559 53873559 53873559 CTGACCCCGTGATCTGCCCGCCTCAGCCTCCCAAAGCGCTGGGACCACAGGCGCGAGCCACCATG CTGACCCCGTGATCTGCCCGCCTCAGCCTCCCGAAGCGCTGGGACCACAGGCGCGAGCCACCATG A G LRRC1 Ensembl:ENSG00000137269 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:53873431..53873558 26863196 MeRIP-seq:(Medium) rs903018236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163,RMVar_hsa_circ_330899,RMVar_hsa_circ_364281,RMVar_hsa_circ_239007 92285 RMVar_ID_92285 Human_SNP_ID_277692898 m1A Human chr6 + 54210202 54210202 54210202 GCCAGAGCAGCTGCTTGTCTGCAGCAGGACACAGTTCCTACATACGTTTCAGTTCTTTCATGGTA GCCAGAGCAGCTGCTTGTCTGCAGCAGGACACGGTTCCTACATACGTTTCAGTTCTTTCATGGTA A G MLIP Ensembl:ENSG00000146147 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs139254516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26861,RMVar_hsa_circ_356542,RMVar_hsa_circ_239018,RMVar_hsa_circ_334360,RMVar_hsa_circ_302058,RMVar_hsa_circ_63697,RMVar_hsa_circ_239020,RMVar_hsa_circ_295015,RMVar_hsa_circ_357155 92286 RMVar_ID_92286 Human_SNP_ID_278386384 m1A Human chr6 - 56954590 56954590 56954590 CCCCGCCGTCGAGTCGCCCTCGCCTCGCCCGCACCATGATCGCCGCGGCTTTCCTCGTCTTGCTG CCCCGCCGTCGAGTCGCCCTCGCCTCGCCCGCGCCATGATCGCCGCGGCTTTCCTCGTCTTGCTG T C DST Ensembl:ENSG00000151914 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:56954541..56954796 26863196 MeRIP-seq:(Medium) rs1172227783 Functional Loss SNV dbSNP153 33..33 33 - - - 92287 RMVar_ID_92287 Human_SNP_ID_278407297 m1A Human chr6 - 57046702 57046702 57046702 AGCACCACTGCTCCTGCTGTCCCTACTGCCGCAGCCGCCACCACTCCCCTTCCCGCCCTGCACCG AGCACCACTGCTCCTGCTGTCCCTACTGCCGCCGCCGCCACCACTCCCCTTCCCGCCCTGCACCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:57046563..57046767 26863196 MeRIP-seq:(Medium) rs201107446 Functional Loss SNV dbSNP153 33..33 33 - - - 92288 RMVar_ID_92288 Human_SNP_ID_278407320 m1A Human chr6 - 57046728 57046728 57046728 CCCATGTCTCCGACGGCCGCGCTGACAGCACCACTGCTCCTGCTGTCCCTACTGCCGCAGCCGCC CCCATGTCTCCGACGGCCGCGCTGACAGCACCTCTGCTCCTGCTGTCCCTACTGCCGCAGCCGCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:57046680..57046806 26863196 MeRIP-seq:(Medium) rs751214126 Functional Loss SNV dbSNP153 33..33 33 - - - 92289 RMVar_ID_92289 Human_SNP_ID_278407321 m1A Human chr6 - 57046728 57046728 57046728 CCCATGTCTCCGACGGCCGCGCTGACAGCACCACTGCTCCTGCTGTCCCTACTGCCGCAGCCGCC CCCATGTCTCCGACGGCCGCGCTGACAGCACCGCTGCTCCTGCTGTCCCTACTGCCGCAGCCGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:57046680..57046806 26863196 MeRIP-seq:(Medium) rs751214126 Functional Loss SNV dbSNP153 33..33 33 - - - 92290 RMVar_ID_92290 Human_SNP_ID_278417558 m1A Human chr6 - 57090190 57090190 57090190 CTCCTGCTGTCCCTGCCGCCGCCGTCGCCACGAATCCCCTTCCCGCCCTGCACCGCCTGGCGCTA CTCCTGCTGTCCCTGCCGCCGCCGTCGCCACGCATCCCCTTCCCGCCCTGCACCGCCTGGCGCTA T G lnc-RAB23-8 RNACentral:URS00009BEC68 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:57090071..57090361 26863196 MeRIP-seq:(Medium) rs893530016 Functional Loss SNV dbSNP153 33..33 33 - - - 92291 RMVar_ID_92291 Human_SNP_ID_278422446 m1A Human chr6 - 57110128 57110128 57110128 CCTCCAGCTGAATGTCTGGCTCCTGTTTCTCCACCAGGCCAACTAACTCTTGCCTAATCATCCTC CCTCCAGCTGAATGTCTGGCTCCTGTTTCTCCGCCAGGCCAACTAACTCTTGCCTAATCATCCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:57110080..57110190 26863196 MeRIP-seq:(Medium) rs1054168124 Functional Loss SNV dbSNP153 33..33 33 - - - 92292 RMVar_ID_92292 Human_SNP_ID_278436469 m1A Human chr6 - 57172361 57172361 57172361 GCAAGTCTCTGAGGCACGGGAGGGGCGGACGCAGAGACCGAGCGCCTAATGTGGCTAGCGGATCG GCAAGTCTCTGAGGCACGGGAGGGGCGGACGCCGAGACCGAGCGCCTAATGTGGCTAGCGGATCG T G ZNF451-AS1 Ensembl:ENSG00000226803 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:57172326..57172500 26863196 MeRIP-seq:(Medium) rs1332035684 Functional Loss SNV dbSNP153 33..33 33 - - - 92293 RMVar_ID_92293 Human_SNP_ID_278440547 m1A Human chr6 + 57189180 57189180 57189180 GTGACAAAATTTATGTCCTGACACATGATTACATATTAAATCATTTTGTAAAAGAAATGATTCTG GTGACAAAATTTATGTCCTGACACATGATTACGTATTAAATCATTTTGTAAAAGAAATGATTCTG A G BAG2 Ensembl:ENSG00000112208 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:57189130..57189280 32194978 MeRIP-seq:(Medium) rs954191542 Functional Loss SNV dbSNP153 33..33 33 - - - 92294 RMVar_ID_92294 Human_SNP_ID_278516281 m1A Human chr6 + 57512007 57512007 57512007 GAGTATAGAGAGACAAGAAAAGGGTGAAGGGTACTGAATCGAACCCACAGAATATCAGTGTTTAA GAGTATAGAGAGACAAGAAAAGGGTGAAGGGTTCTGAATCGAACCCACAGAATATCAGTGTTTAA A T PRIM2 Ensembl:ENSG00000146143 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:57511958..57512070 26863196 MeRIP-seq:(Medium) rs1554347747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43753,RMVar_hsa_circ_331015,RMVar_hsa_circ_57631,RMVar_hsa_circ_291484,RMVar_hsa_circ_306755 92295 RMVar_ID_92295 Human_SNP_ID_278568102 m1A Human chr6 - 57792848 57792848 57792848 GCTCCCTTAGCATGCGAGAGGTAGCGGGATCGACGCCCGCATTCTCTAATTTCTTGTCTGGTTTA GCTCCCTTAGCATGCGAGAGGTAGCGGGATCGGCGCCCGCATTCTCTAATTTCTTGTCTGGTTTA T C TRA-AGC22-1-001,tRNA-Ala-AGC-22-1 RNACentral:URS00006E5A57,RNACentral:URS0000693544 tRNA,tRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1279420787 Functional Loss SNV dbSNP153 33..33 33 - - - 92296 RMVar_ID_92296 Human_SNP_ID_278568399 m1A Human chr6 - 57793560 57793560 57793560 GCCTGCTTAGCATGCAAGAGGTAGCAGGATCGATGCCTGCATTCTCCAGCTTCTTTTAATCCCTA GCCTGCTTAGCATGCAAGAGGTAGCAGGATCGGTGCCTGCATTCTCCAGCTTCTTTTAATCCCTA T C tRNA-Ala-AGC-19-1 RNACentral:URS00006E6B1E tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1430207813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_666820,Human_RBP_ID_1675356,Human_RBP_ID_8271621,Human_RBP_ID_8647878,Human_RBP_ID_15862225,Human_RBP_ID_18539897,Human_RBP_ID_21359900,Human_RBP_ID_22832113,Human_RBP_ID_23139133,Human_RBP_ID_27100063 92297 RMVar_ID_92297 Human_SNP_ID_278580549 m1A Human chr6 - 57842229 57842229 57842229 GTCAGTTTCATAATCTGAAAGTCCTGAGTTCAAGCCTCAGAGAGGGCATCACTTTTGCCAAAGAA GTCAGTTTCATAATCTGAAAGTCCTGAGTTCAGGCCTCAGAGAGGGCATCACTTTTGCCAAAGAA T C tRNA-Met-CAT-7-1 RNACentral:URS000065DEBF tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1432559271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5268973,Human_RBP_ID_18519741,Human_RBP_ID_23139140 92298 RMVar_ID_92298 Human_SNP_ID_278584965 m1A Human chr6 - 57861181 57861181 57861181 GCTTGCTTAGCATGCAAGAGGTAGTGGGATCGATGCCCACATTCTCCAAACTTTATTATTTAGAC GCTTGCTTAGCATGCAAGAGGTAGTGGGATCGGTGCCCACATTCTCCAAACTTTATTATTTAGAC T C tRNA-Ala-AGC-17-1,lnc-RAB23-17 RNACentral:URS00006A7FD7,RNACentral:URS00008BE4AD tRNA,lincRNA exon,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1241633703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8944112 92299 RMVar_ID_92299 Human_SNP_ID_278609326 m1A Human chr6 - 57961635 57961635 57961635 AGATTACGCCACTGTACTGCAGCCTGGGCGACAGAGGCTCTGGCTTTAAAAAAAAAAAAAAAGGG AGATTACGCCACTGTACTGCAGCCTGGGCGACGGAGGCTCTGGCTTTAAAAAAAAAAAAAAAGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:57961606..57961693 26863410 MeRIP-seq:(Medium) rs1345538231 Functional Loss SNV dbSNP153 33..33 33 - - - 92300 RMVar_ID_92300 Human_SNP_ID_518019964 m1A Human chr12 + 120070762 120070762 120070762 ACTCTTTTTTTTTTTTTTTGAGACGGAGTTTCATTCTTGTCGCCCAGGCTGGAGTGCAATGGCGC ACTCTTTTTTTTTTTTTTTGAGACGGAGTTTCTTTCTTGTCGCCCAGGCTGGAGTGCAATGGCGC A T BICDL1 Ensembl:ENSG00000135127 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:120070730..120070817 26863410 MeRIP-seq:(Medium) rs1433118772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60580,RMVar_hsa_circ_160646,RMVar_hsa_circ_357395,RMVar_hsa_circ_28637 92301 RMVar_ID_92301 Human_SNP_ID_518026525 m1A Human chr12 + 120095532 120095532 120095532 GCACCGTGCATCCTCAGGGCCCGTGGCCAACCAGGACAGTCCCAAGGACGGAGACCCCGCTTCTG GCACCGTGCATCCTCAGGGCCCGTGGCCAACCGGGACAGTCCCAAGGACGGAGACCCCGCTTCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120095445..120095754 26863196 MeRIP-seq:(Medium) rs1350224286 Functional Loss SNV dbSNP153 33..33 33 - - - 92302 RMVar_ID_92302 Human_SNP_ID_518026656 m1A Human chr12 - 120095999 120095999 120095999 GCGGCCAGTTTTGACACGCCCCAGTGCCCTGGAGAACAACCAGGGTCATCTGCACTTGATGACTG GCGGCCAGTTTTGACACGCCCCAGTGCCCTGGGGAACAACCAGGGTCATCTGCACTTGATGACTG T C RAB35 Ensembl:ENSG00000111737 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120095948..120096015 26863196 MeRIP-seq:(Medium) rs1036282404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26421723 Human_miRNA_ID_1539373 92303 RMVar_ID_92303 Human_SNP_ID_518027003 m1A Human chr12 - 120096955 120096955 120096955 GCCGAGCGGACTGATTCGCAGAGTCTGTACATAGTGTATATTGCTCTACCCGGCCGCACACCACG GCCGAGCGGACTGATTCGCAGAGTCTGTACATCGTGTATATTGCTCTACCCGGCCGCACACCACG T G RAB35 Ensembl:ENSG00000111737 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120096905..120097000 26863196 MeRIP-seq:(Medium) rs561118334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412098,Human_RBP_ID_1788487,Human_RBP_ID_2308777,Human_RBP_ID_3395406,Human_RBP_ID_21884822,Human_RBP_ID_27418959 92304 RMVar_ID_92304 Human_SNP_ID_518027207 m1A Human chr12 - 120097366 120097366 120097366 GGCCCTTCCTCTTTCCTCTCCACAGATGTTCAACTGCATCACGGAGCTGGTCCTCCGAGCAAAGA GGCCCTTCCTCTTTCCTCTCCACAGATGTTCAGCTGCATCACGGAGCTGGTCCTCCGAGCAAAGA T C RAB35 Ensembl:ENSG00000111737 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs761499454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875232 Human_Splice_Rec_1432228,Human_Splice_Rec_1432240,Human_Splice_Rec_1432248,Human_Splice_Rec_1432258,Human_Splice_Rec_1432264 92305 RMVar_ID_92305 Human_SNP_ID_518032362 m1A Human chr12 - 120116666 120116666 120116666 GAGGCCAGTACCGACCCCGCCCGCCCGCGCGCACCGCCCCCGCCCGCCATGGCCCGGGACTACGA GAGGCCAGTACCGACCCCGCCCGCCCGCGCGCCCCGCCCCCGCCCGCCATGGCCCGGGACTACGA T G RAB35 Ensembl:ENSG00000111737 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120116626..120116813 26863196 MeRIP-seq:(Medium) rs1056840256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4204399,Human_RBP_ID_5171342,Human_RBP_ID_23256009 Human_Splice_Rec_1432219,Human_Splice_Rec_1432229,Human_Splice_Rec_1432241,Human_Splice_Rec_1432249,Human_Splice_Rec_1432265 92306 RMVar_ID_92306 Human_SNP_ID_518032541 m1A Human chr12 - 120117003 120117003 120117003 CAGCGGCTCGGCTCCGCAAGCTCTCAGCGCCCAGGGTGGCGGCGACGACGCTCCCCGAGGAGACG CAGCGGCTCGGCTCCGCAAGCTCTCAGCGCCCCGGGTGGCGGCGACGACGCTCCCCGAGGAGACG T G RAB35 Ensembl:ENSG00000111737 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120116952..120117357 26863196 MeRIP-seq:(Medium) rs1330225570 Functional Loss SNV dbSNP153 33..33 33 - - - 92307 RMVar_ID_92307 Human_SNP_ID_518032556 m1A Human chr12 + 120117039 120117039 120117039 CGCTGAGAGCTTGCGGAGCCGAGCCGCTGTCGAGTCCCAGCGGAAAGAAGCCCAAGGTGCCGGAG CGCTGAGAGCTTGCGGAGCCGAGCCGCTGTCGTGTCCCAGCGGAAAGAAGCCCAAGGTGCCGGAG A T AC004812.2 Ensembl:ENSG00000277283 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120116993..120117084 26863196 MeRIP-seq:(Medium) rs1268809340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247038 92308 RMVar_ID_92308 Human_SNP_ID_518040748 m1A Human chr12 + 120147069 120147069 120147069 CAGCTGGGCCGCTACCTTCTGGTCTGTCAGGGAGTACATGTTGCCAATAATCTGGGCTGCCATCT CAGCTGGGCCGCTACCTTCTGGTCTGTCAGGGTGTACATGTTGCCAATAATCTGGGCTGCCATCT A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120147051..120147125 26863196 MeRIP-seq:(Medium) rs748941770 Functional Loss SNV dbSNP153 33..33 33 - - - 92309 RMVar_ID_92309 Human_SNP_ID_518044522 m1A Human chr12 - 120160229 120160228 120160230 CTTTAGGAGATAAAGAAGAAGAAAGGCATCAAAGAGGAGGTGCAGCTGACCAGCAAGCAGAAGGA CTTTAGGAGATAAAGAAGAAGAAAGGCATCA__GAGGAGGTGCAGCTGACCAGCAAGCAGAAGGA CTT C GCN1 Ensembl:ENSG00000089154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120160126..120160286 26863196 MeRIP-seq:(Medium) rs775760259 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_872671,Human_RBP_ID_1479626,Human_RBP_ID_18976274,Human_RBP_ID_22645453,Human_RBP_ID_24543505,Human_RBP_ID_26322152,Human_RBP_ID_26901893,Human_RBP_ID_27807274 Human_Splice_Rec_1432312,Human_Splice_Rec_1432313,Human_Splice_Rec_1432399,Human_Splice_Rec_1432408,Human_Splice_Rec_1432409 RMVar_hsa_circ_93383,RMVar_hsa_circ_113123,RMVar_hsa_circ_160658,RMVar_hsa_circ_160672,RMVar_hsa_circ_160659,RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_127865,RMVar_hsa_circ_82818,RMVar_hsa_circ_160670,RMVar_hsa_circ_124983,RMVar_hsa_circ_160673,RMVar_hsa_circ_117599,RMVar_hsa_circ_160679,RMVar_hsa_circ_116765,RMVar_hsa_circ_160680,RMVar_hsa_circ_160682,RMVar_hsa_circ_121223,RMVar_hsa_circ_160690,RMVar_hsa_circ_101318,RMVar_hsa_circ_123642,RMVar_hsa_circ_118731,RMVar_hsa_circ_96078,RMVar_hsa_circ_99907,RMVar_hsa_circ_160692,RMVar_hsa_circ_160694,RMVar_hsa_circ_160693,RMVar_hsa_circ_160691,RMVar_hsa_circ_11802,RMVar_hsa_circ_121604,RMVar_hsa_circ_86722,RMVar_hsa_circ_98244,RMVar_hsa_circ_160703,RMVar_hsa_circ_160702,RMVar_hsa_circ_121514,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160711,RMVar_hsa_circ_160712,RMVar_hsa_circ_160710,RMVar_hsa_circ_112828,RMVar_hsa_circ_160716,RMVar_hsa_circ_85377,RMVar_hsa_circ_91241,RMVar_hsa_circ_80851,RMVar_hsa_circ_8132,RMVar_hsa_circ_160717,RMVar_hsa_circ_160718,RMVar_hsa_circ_160719,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_160722,RMVar_hsa_circ_118394,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_107761,RMVar_hsa_circ_348583,RMVar_hsa_circ_34195,RMVar_hsa_circ_160724 92310 RMVar_ID_92310 Human_SNP_ID_518048567 m1A Human chr12 + 120174121 120174121 120174121 GGATGAACAGCTCAGCCACGATCCCATTCAGGACCTGACTGGAAGGTCCAGACACCACGTGATGA GGATGAACAGCTCAGCCACGATCCCATTCAGGCCCTGACTGGAAGGTCCAGACACCACGTGATGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120174051..120174125 32194978 MeRIP-seq:(Medium) rs1479631360 Functional Loss SNV dbSNP153 33..33 33 - - - 92311 RMVar_ID_92311 Human_SNP_ID_518053233 m1A Human chr12 - 120190389 120190389 120190389 TCTGTTGCTTGGCCTTCACAGGTTTCCGAGACACTAAAGCGTTTTGCAGGGAAGGTGACAACAGC TCTGTTGCTTGGCCTTCACAGGTTTCCGAGACGCTAAAGCGTTTTGCAGGGAAGGTGACAACAGC T C GCN1 Ensembl:ENSG00000089154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120190276..120190425 26863196 MeRIP-seq:(Medium) rs1191315487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247040,Human_RBP_ID_24938189 Human_Splice_Rec_1432272,Human_Splice_Rec_1432273 RMVar_hsa_circ_47903,RMVar_hsa_circ_80413,RMVar_hsa_circ_328382,RMVar_hsa_circ_160738,RMVar_hsa_circ_160739,RMVar_hsa_circ_160743,RMVar_hsa_circ_83250,RMVar_hsa_circ_95142,RMVar_hsa_circ_98067,RMVar_hsa_circ_160748,RMVar_hsa_circ_160747,RMVar_hsa_circ_87849,RMVar_hsa_circ_370883,RMVar_hsa_circ_160750,RMVar_hsa_circ_160751,RMVar_hsa_circ_61267 92312 RMVar_ID_92312 Human_SNP_ID_518056464 m1A Human chr12 - 120200829 120200829 120200829 ACCAGGCCTGAGCTCCCTGTCTCTCCTCAGTGACATCGTCTTTAAACCCTGCGTGGCAATCCCTG ACCAGGCCTGAGCTCCCTGTCTCTCCTCAGTGGCATCGTCTTTAAACCCTGCGTGGCAATCCCTG T C RPLP0 Ensembl:ENSG00000089157 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK-293T cells,m1A-IP-seq;HEK293T,ALKBH3 KO chr12:120200704..120200900 31548705,26863410 m1A-IP-seq:(High) rs948873913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412180,Human_RBP_ID_753085,Human_RBP_ID_1164990,Human_RBP_ID_1356278,Human_RBP_ID_1465865,Human_RBP_ID_1788644,Human_RBP_ID_3395499,Human_RBP_ID_4204840,Human_RBP_ID_8367224,Human_RBP_ID_18188942,Human_RBP_ID_22170514,Human_RBP_ID_22795654,Human_RBP_ID_26806218,Human_RBP_ID_26901963,Human_RBP_ID_27210732,Human_RBP_ID_27425856 Human_Splice_Rec_1432419,Human_Splice_Rec_1432432,Human_Splice_Rec_1432433,Human_Splice_Rec_1432448,Human_Splice_Rec_1432449,Human_Splice_Rec_1432460,Human_Splice_Rec_1432461,Human_Splice_Rec_1432484,Human_Splice_Rec_1432485,Human_Splice_Rec_1432498,Human_Splice_Rec_1432512,Human_Splice_Rec_1432513,Human_Splice_Rec_1432525,Human_Splice_Rec_1432535,Human_Splice_Rec_1432545,Human_Splice_Rec_1432555,Human_Splice_Rec_1432566,Human_Splice_Rec_1432567,Human_Splice_Rec_1432577,Human_Splice_Rec_1432581,Human_Splice_Rec_1432588,Human_Splice_Rec_1432589,Human_Splice_Rec_1432599,Human_Splice_Rec_1432607,Human_Splice_Rec_1432614,Human_Splice_Rec_1432627,Human_Splice_Rec_1432634,Human_Splice_Rec_1432640,Human_Splice_Rec_1432641,Human_Splice_Rec_1432645 Human_miRNA_ID_2950546,Human_miRNA_ID_2950547,Human_miRNA_ID_2950548 RMVar_hsa_circ_101737,RMVar_hsa_circ_160761,RMVar_hsa_circ_117872,RMVar_hsa_circ_160764,RMVar_hsa_circ_127168,RMVar_hsa_circ_1983,RMVar_hsa_circ_160767,RMVar_hsa_circ_160769,RMVar_hsa_circ_102143 92313 RMVar_ID_92313 Human_SNP_ID_518059573 m1A Human chr12 - 120211379 120211379 120211379 GTATTTTATTGTTTCTTAGCACAAGCAGGTGAACTGGGAGCAGCTCTGTGACTCCCCCTCTTTCA GTATTTTATTGTTTCTTAGCACAAGCAGGTGAGCTGGGAGCAGCTCTGTGACTCCCCCTCTTTCA T C PXN Ensembl:ENSG00000089159 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:120211301..120211425 26863196 MeRIP-seq:(Medium) rs1322716732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412210,Human_RBP_ID_17236448,Human_RBP_ID_17357757,Human_RBP_ID_21884824,Human_RBP_ID_24464251 92314 RMVar_ID_92314 Human_SNP_ID_518059714 m1A Human chr12 - 120211897 120211897 120211897 TGGGGTCTCTTTTTATCCTTATTCCTCCCCCGACCTAATTGTCTTTGTTCTGTGATTATTGGGGG TGGGGTCTCTTTTTATCCTTATTCCTCCCCCGGCCTAATTGTCTTTGTTCTGTGATTATTGGGGG T C PXN Ensembl:ENSG00000089159 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120211851..120211900 32194978 MeRIP-seq:(Medium) rs1453822705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5490998,Human_RBP_ID_16989075,Human_RBP_ID_17810871,Human_RBP_ID_24464253,Human_RBP_ID_26412622 92315 RMVar_ID_92315 Human_SNP_ID_518059754 m1A Human chr12 + 120211988 120211984 120211989 CCCCGGCTGCACTGCTGAAATATGAGGAAGAGATGGCTCCAGTGTGGGGTGCTGGCCAGGCCAGT CCCCGGCTGCACTGCTGAAATATGAGGAA_____GGCTCCAGTGTGGGGTGCTGGCCAGGCCAGT AGAGAT A PXN-AS1 Ensembl:ENSG00000255857 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:120211938..120212081;chr12:120211938..120212024 26863196 MeRIP-seq:(Medium) rs776054329 Functional Loss DEL dbSNP153 30..34 33 - - - 92316 RMVar_ID_92316 Human_SNP_ID_518059772 m1A Human chr12 - 120212020 120212020 120212020 GGCTCCACCCCAGCCCATGTACGTCCCCACGAACTGGCCTGGCCAGCACCCCACACTGGAGCCAT GGCTCCACCCCAGCCCATGTACGTCCCCACGATCTGGCCTGGCCAGCACCCCACACTGGAGCCAT T A PXN Ensembl:ENSG00000089159 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:120211972..120212099 26863196 MeRIP-seq:(Medium) rs367774069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8367233,Human_RBP_ID_17357409,Human_RBP_ID_27419014 92317 RMVar_ID_92317 Human_SNP_ID_518059775 m1A Human chr12 - 120212024 120212023 120212024 TGGGGGCTCCACCCCAGCCCATGTACGTCCCCACGAACTGGCCTGGCCAGCACCCCACACTGGAG TGGGGGCTCCACCCCAGCCCATGTACGTCCCC_CGAACTGGCCTGGCCAGCACCCCACACTGGAG GT G PXN Ensembl:ENSG00000089159 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120211976..120212577 32194978 MeRIP-seq:(Medium) rs1373196678 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8367233,Human_RBP_ID_17357409,Human_RBP_ID_23541897 Human_miRNA_ID_841947,Human_miRNA_ID_1417822 92318 RMVar_ID_92318 Human_SNP_ID_518060626 m1A Human chr12 - 120214934 120214932 120214935 CGAGCACTTCGTCTGCACCCACTGCCAGGAGGAGATCGGATCCCGGAACTTCTTCGAGCGGGATG CGAGCACTTCGTCTGCACCCACTGCCAGGAG___ATCGGATCCCGGAACTTCTTCGAGCGGGATG TCTC T PXN Ensembl:ENSG00000089159 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120214838..120215192 32194978 MeRIP-seq:(Medium) rs1566354869 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_33653,Human_RBP_ID_8787440 Human_Splice_Rec_1432706,Human_Splice_Rec_1432726,Human_Splice_Rec_1432748,Human_Splice_Rec_1432768,Human_Splice_Rec_1432780,Human_Splice_Rec_1432802,Human_Splice_Rec_1432824,Human_Splice_Rec_1432842,Human_Splice_Rec_1432866,Human_Splice_Rec_1432878 RMVar_hsa_circ_19844,RMVar_hsa_circ_85880,RMVar_hsa_circ_160771,RMVar_hsa_circ_370560,RMVar_hsa_circ_160773,RMVar_hsa_circ_75592,RMVar_hsa_circ_345196,RMVar_hsa_circ_160774 92319 RMVar_ID_92319 Human_SNP_ID_518061359 m1A Human chr12 - 120216842 120216832 120216843 TGGGAAGCGGGCCGGGGGGCAGCTCGTAGAGAAGGTGGCGAGGAGATGCCCATGGCTGGGGCTGG TGGGAAGCGGGCCGGGGGGCAGCTCGTAGAG___________GAGATGCCCATGGCTGGGGCTGG CCTCGCCACCTT C PXN Ensembl:ENSG00000089159 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120216818..120217015 26863196 MeRIP-seq:(Medium) rs753967042 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_809690,Human_RBP_ID_872682,Human_RBP_ID_21967164,Human_RBP_ID_22436140,Human_RBP_ID_24551250 Human_Splice_Rec_1432861 RMVar_hsa_circ_19844,RMVar_hsa_circ_160771,RMVar_hsa_circ_370560,RMVar_hsa_circ_126431,RMVar_hsa_circ_160775 92320 RMVar_ID_92320 Human_SNP_ID_518061364 m1A Human chr12 - 120216842 120216842 120216842 TGGGAAGCGGGCCGGGGGGCAGCTCGTAGAGAAGGTGGCGAGGAGATGCCCATGGCTGGGGCTGG TGGGAAGCGGGCCGGGGGGCAGCTCGTAGAGACGGTGGCGAGGAGATGCCCATGGCTGGGGCTGG T G PXN Ensembl:ENSG00000089159 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120216818..120217015 26863196 MeRIP-seq:(Medium) rs1476971000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809690,Human_RBP_ID_872682,Human_RBP_ID_21967164,Human_RBP_ID_22436140,Human_RBP_ID_24551250 Human_Splice_Rec_1432861 RMVar_hsa_circ_19844,RMVar_hsa_circ_160771,RMVar_hsa_circ_370560,RMVar_hsa_circ_126431,RMVar_hsa_circ_160775 92321 RMVar_ID_92321 Human_SNP_ID_518063010 m1A Human chr12 + 120222615 120222615 120222615 AGAGACTCTCCACACTGGGCCGCACGTCCTCCAGGCCCCGGCCCCCATTCCGCTTAGGCTTCTCT AGAGACTCTCCACACTGGGCCGCACGTCCTCCGGGCCCCGGCCCCCATTCCGCTTAGGCTTCTCT A G AC004263.2 Ensembl:ENSG00000286067 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120222532..120222617 26863196 MeRIP-seq:(Medium) rs891382407 Functional Loss SNV dbSNP153 33..33 33 - - - 92322 RMVar_ID_92322 Human_SNP_ID_518065614 m1A Human chr12 - 120232963 120232963 120232963 ACTTAGTGACCAGCTAAATGTGGGAGCTATTAAAGGGACTTAGAAAAGAGAACTGGGGAAGTCAG ACTTAGTGACCAGCTAAATGTGGGAGCTATTATAGGGACTTAGAAAAGAGAACTGGGGAAGTCAG T A PXN Ensembl:ENSG00000089159 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120232960..120233114 26863196 MeRIP-seq:(Medium) rs749800424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2308923 92323 RMVar_ID_92323 Human_SNP_ID_518065621 m1A Human chr12 + 120233003 120233003 120233003 TCCCACATTTAGCTGGTCACTAAGTCACATCAATTCTTCCTTCGCGGGGCCTCTCCCTGTCATCA TCCCACATTTAGCTGGTCACTAAGTCACATCAGTTCTTCCTTCGCGGGGCCTCTCCCTGTCATCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120232997..120233192 26863196 MeRIP-seq:(Medium) rs1566409875 Functional Loss SNV dbSNP153 33..33 33 - - - 92324 RMVar_ID_92324 Human_SNP_ID_518065776 m1A Human chr12 + 120233763 120233763 120233763 TTCTTGACCCTCTCAGAATATGGCCCCAAACTAACCTTCACTGCCTCCTTGGTCCCCCTCACTGC TTCTTGACCCTCTCAGAATATGGCCCCAAACTGACCTTCACTGCCTCCTTGGTCCCCCTCACTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120233760..120233869 26863196 MeRIP-seq:(Medium) rs1385233274 Functional Loss SNV dbSNP153 33..33 33 - - - 92325 RMVar_ID_92325 Human_SNP_ID_518067446 m1A Human chr12 + 120240793 120240793 120240793 CTCCTAACTCTGCCAGAGCATTCGCCATTGGAACATCGACACTAACCCACCCAGGACTGACTCCA CTCCTAACTCTGCCAGAGCATTCGCCATTGGAGCATCGACACTAACCCACCCAGGACTGACTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120240788..120240853 26863196 MeRIP-seq:(Medium) rs546968760 Functional Loss SNV dbSNP153 33..33 33 - - - 92326 RMVar_ID_92326 Human_SNP_ID_518069538 m1A Human chr12 + 120249431 120249431 120249431 CATTAGGAGGGAAAATCTCAGACAGTCGAAGCAGGGAGAAGAGGAAGGACAGAGCCCAAGCCAGT CATTAGGAGGGAAAATCTCAGACAGTCGAAGCGGGGAGAAGAGGAAGGACAGAGCCCAAGCCAGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120249428..120249562 32194978 MeRIP-seq:(Medium) rs905955731 Functional Loss SNV dbSNP153 33..33 33 - - - 92327 RMVar_ID_92327 Human_SNP_ID_518078229 m1A Human chr12 - 120282530 120282530 120282530 CCTGGCTTAGAATCTGCTGGATTGGTCTCCCCAAGCATCACTCGGCCTGTCTTCACGACGTTCAG CCTGGCTTAGAATCTGCTGGATTGGTCTCCCCCAGCATCACTCGGCCTGTCTTCACGACGTTCAG T G lnc-PXN-1,RF00017-049,RF00017-1304 RNACentral:URS00008C12D4,RNACentral:URS000096B6E3,RNACentral:URS0000990DE9 lincRNA,SRP RNA,SRP RNA exon,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120282527..120282614 26863196 MeRIP-seq:(Medium) rs1342586901 Functional Loss SNV dbSNP153 33..33 33 - - - 92328 RMVar_ID_92328 Human_SNP_ID_518081184 m1A Human chr12 - 120291850 120291850 120291850 CGTAGCCAATGAGGTTTATCCGAGGCGCGATTATTGCTAATTGAAAACTTTTCCCAATACCCCGC CGTAGCCAATGAGGTTTATCCGAGGCGCGATTTTTGCTAATTGAAAACTTTTCCCAATACCCCGC T A RNU4-2 Ensembl:ENSG00000202538 snRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:120291765..120291896 26863196 MeRIP-seq:(Medium) rs1429747184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275034,Human_RBP_ID_412244,Human_RBP_ID_1082697,Human_RBP_ID_1164998,Human_RBP_ID_1235675,Human_RBP_ID_1267411,Human_RBP_ID_1356287,Human_RBP_ID_1465876,Human_RBP_ID_1788655,Human_RBP_ID_2308952,Human_RBP_ID_3395525,Human_RBP_ID_4250797,Human_RBP_ID_5174046,Human_RBP_ID_5491005,Human_RBP_ID_5554711,Human_RBP_ID_6142029,Human_RBP_ID_8066081,Human_RBP_ID_8247494,Human_RBP_ID_8367273,Human_RBP_ID_8776965,Human_RBP_ID_9012160,Human_RBP_ID_9711730,Human_RBP_ID_11842008,Human_RBP_ID_17062416,Human_RBP_ID_17067265,Human_RBP_ID_17111892,Human_RBP_ID_17186764,Human_RBP_ID_17667688,Human_RBP_ID_17683512,Human_RBP_ID_17832092,Human_RBP_ID_18174135,Human_RBP_ID_18176675,Human_RBP_ID_18199044,Human_RBP_ID_18206234,Human_RBP_ID_18256051,Human_RBP_ID_18433666,Human_RBP_ID_18511055,Human_RBP_ID_18527550,Human_RBP_ID_18619507,Human_RBP_ID_19826335,Human_RBP_ID_22036559,Human_RBP_ID_22170528,Human_RBP_ID_22382576,Human_RBP_ID_22492448,Human_RBP_ID_22793250,Human_RBP_ID_22911151,Human_RBP_ID_23110230,Human_RBP_ID_23268431,Human_RBP_ID_23541942,Human_RBP_ID_24464261,Human_RBP_ID_24551380,Human_RBP_ID_24938342,Human_RBP_ID_26412651,Human_RBP_ID_26609009,Human_RBP_ID_26747946,Human_RBP_ID_26901995,Human_RBP_ID_27210753,Human_RBP_ID_27419038,Human_RBP_ID_27623673 Human_miRNA_ID_3136562,Human_miRNA_ID_3137748,Human_miRNA_ID_3138178 92329 RMVar_ID_92329 Human_SNP_ID_518081186 m1A Human chr12 - 120291853 120291853 120291853 TATCGTAGCCAATGAGGTTTATCCGAGGCGCGATTATTGCTAATTGAAAACTTTTCCCAATACCC TATCGTAGCCAATGAGGTTTATCCGAGGCGCGGTTATTGCTAATTGAAAACTTTTCCCAATACCC T C RNU4-2 Ensembl:ENSG00000202538 snRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120291765..120291931 26863196 MeRIP-seq:(Medium) rs553906182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275034,Human_RBP_ID_412244,Human_RBP_ID_1082697,Human_RBP_ID_1164998,Human_RBP_ID_1235675,Human_RBP_ID_1267411,Human_RBP_ID_1356287,Human_RBP_ID_1465876,Human_RBP_ID_1788655,Human_RBP_ID_2308952,Human_RBP_ID_3395525,Human_RBP_ID_4250797,Human_RBP_ID_5174046,Human_RBP_ID_5491005,Human_RBP_ID_5554711,Human_RBP_ID_5640983,Human_RBP_ID_6142029,Human_RBP_ID_8066081,Human_RBP_ID_8247494,Human_RBP_ID_8367273,Human_RBP_ID_8776965,Human_RBP_ID_9012160,Human_RBP_ID_9277145,Human_RBP_ID_9711730,Human_RBP_ID_11842008,Human_RBP_ID_17062416,Human_RBP_ID_17067265,Human_RBP_ID_17111892,Human_RBP_ID_17186764,Human_RBP_ID_17667688,Human_RBP_ID_17683512,Human_RBP_ID_17832092,Human_RBP_ID_18174135,Human_RBP_ID_18176675,Human_RBP_ID_18199044,Human_RBP_ID_18206234,Human_RBP_ID_18256051,Human_RBP_ID_18433666,Human_RBP_ID_18511055,Human_RBP_ID_18527550,Human_RBP_ID_18619507,Human_RBP_ID_19826335,Human_RBP_ID_22036559,Human_RBP_ID_22170528,Human_RBP_ID_22382576,Human_RBP_ID_22492448,Human_RBP_ID_22793250,Human_RBP_ID_22911151,Human_RBP_ID_23110230,Human_RBP_ID_23125169,Human_RBP_ID_23268431,Human_RBP_ID_23541942,Human_RBP_ID_24464261,Human_RBP_ID_24551380,Human_RBP_ID_24938342,Human_RBP_ID_26412651,Human_RBP_ID_26609009,Human_RBP_ID_26747946,Human_RBP_ID_26901995,Human_RBP_ID_27210753,Human_RBP_ID_27419039,Human_RBP_ID_27623673 Human_miRNA_ID_3136562,Human_miRNA_ID_3137748,Human_miRNA_ID_3138178 92330 RMVar_ID_92330 Human_SNP_ID_518081187 m1A Human chr12 - 120291853 120291853 120291853 TATCGTAGCCAATGAGGTTTATCCGAGGCGCGATTATTGCTAATTGAAAACTTTTCCCAATACCC TATCGTAGCCAATGAGGTTTATCCGAGGCGCGCTTATTGCTAATTGAAAACTTTTCCCAATACCC T G RNU4-2 Ensembl:ENSG00000202538 snRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120291765..120291931 26863196 MeRIP-seq:(Medium) rs553906182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275034,Human_RBP_ID_412244,Human_RBP_ID_1082697,Human_RBP_ID_1164998,Human_RBP_ID_1235675,Human_RBP_ID_1267411,Human_RBP_ID_1356287,Human_RBP_ID_1465876,Human_RBP_ID_1788655,Human_RBP_ID_2308952,Human_RBP_ID_3395525,Human_RBP_ID_4250797,Human_RBP_ID_5174046,Human_RBP_ID_5491005,Human_RBP_ID_5554711,Human_RBP_ID_5640983,Human_RBP_ID_6142029,Human_RBP_ID_8066081,Human_RBP_ID_8247494,Human_RBP_ID_8367273,Human_RBP_ID_8776965,Human_RBP_ID_9012160,Human_RBP_ID_9277145,Human_RBP_ID_9711730,Human_RBP_ID_11842008,Human_RBP_ID_17062416,Human_RBP_ID_17067265,Human_RBP_ID_17111892,Human_RBP_ID_17186764,Human_RBP_ID_17667688,Human_RBP_ID_17683512,Human_RBP_ID_17832092,Human_RBP_ID_18174135,Human_RBP_ID_18176675,Human_RBP_ID_18199044,Human_RBP_ID_18206234,Human_RBP_ID_18256051,Human_RBP_ID_18433666,Human_RBP_ID_18511055,Human_RBP_ID_18527550,Human_RBP_ID_18619507,Human_RBP_ID_19826335,Human_RBP_ID_22036559,Human_RBP_ID_22170528,Human_RBP_ID_22382576,Human_RBP_ID_22492448,Human_RBP_ID_22793250,Human_RBP_ID_22911151,Human_RBP_ID_23110230,Human_RBP_ID_23125169,Human_RBP_ID_23268431,Human_RBP_ID_23541942,Human_RBP_ID_24464261,Human_RBP_ID_24551380,Human_RBP_ID_24938342,Human_RBP_ID_26412651,Human_RBP_ID_26609009,Human_RBP_ID_26747946,Human_RBP_ID_26901995,Human_RBP_ID_27210753,Human_RBP_ID_27419039,Human_RBP_ID_27623673 Human_miRNA_ID_3136562,Human_miRNA_ID_3137748,Human_miRNA_ID_3138178 92331 RMVar_ID_92331 Human_SNP_ID_518081238 m1A Human chr12 + 120291883 120291883 120291883 AATCGCGCCTCGGATAAACCTCATTGGCTACGATACTGCCACTGCGCAAAGCTGGAAAGGTTCTG AATCGCGCCTCGGATAAACCTCATTGGCTACGCTACTGCCACTGCGCAAAGCTGGAAAGGTTCTG A C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:120291797..120291882 26863410 MeRIP-seq:(Medium) rs1017668573 Functional Loss SNV dbSNP153 33..33 33 - - - 92332 RMVar_ID_92332 Human_SNP_ID_518081239 m1A Human chr12 + 120291883 120291883 120291883 AATCGCGCCTCGGATAAACCTCATTGGCTACGATACTGCCACTGCGCAAAGCTGGAAAGGTTCTG AATCGCGCCTCGGATAAACCTCATTGGCTACGGTACTGCCACTGCGCAAAGCTGGAAAGGTTCTG A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:120291797..120291882 26863410 MeRIP-seq:(Medium) rs1017668573 Functional Loss SNV dbSNP153 33..33 33 - - - 92333 RMVar_ID_92333 Human_SNP_ID_518082333 m1A Human chr12 + 120293141 120293141 120293141 CTGTCAAAAATTGCCAGTGCCGACTATATTGCAAGTCGTCACGGCGGGGTATTGGGAAAAGTTTT CTGTCAAAAATTGCCAGTGCCGACTATATTGCCAGTCGTCACGGCGGGGTATTGGGAAAAGTTTT A C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:120293121..120293205 26863410 MeRIP-seq:(Medium) rs1420025948 Functional Loss SNV dbSNP153 33..33 33 - - - 92334 RMVar_ID_92334 Human_SNP_ID_518082354 m1A Human chr12 + 120293149 120293149 120293149 AATTGCCAGTGCCGACTATATTGCAAGTCGTCACGGCGGGGTATTGGGAAAAGTTTTCAATTAGC AATTGCCAGTGCCGACTATATTGCAAGTCGTCCCGGCGGGGTATTGGGAAAAGTTTTCAATTAGC A C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:120293101..120293225;chr12:120293101..120293234;chr12:120293086..120293213 26863196 MeRIP-seq:(Medium) rs868323850 Functional Loss SNV dbSNP153 33..33 33 - - - 92335 RMVar_ID_92335 Human_SNP_ID_518082355 m1A Human chr12 + 120293149 120293149 120293149 AATTGCCAGTGCCGACTATATTGCAAGTCGTCACGGCGGGGTATTGGGAAAAGTTTTCAATTAGC AATTGCCAGTGCCGACTATATTGCAAGTCGTCGCGGCGGGGTATTGGGAAAAGTTTTCAATTAGC A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:120293101..120293225;chr12:120293101..120293234;chr12:120293086..120293213 26863196 MeRIP-seq:(Medium) rs868323850 Functional Loss SNV dbSNP153 33..33 33 - - - 92336 RMVar_ID_92336 Human_SNP_ID_518082356 m1A Human chr12 + 120293149 120293149 120293149 AATTGCCAGTGCCGACTATATTGCAAGTCGTCACGGCGGGGTATTGGGAAAAGTTTTCAATTAGC AATTGCCAGTGCCGACTATATTGCAAGTCGTCTCGGCGGGGTATTGGGAAAAGTTTTCAATTAGC A T RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr12:120293101..120293225;chr12:120293101..120293234;chr12:120293086..120293213 26863196 MeRIP-seq:(Medium) rs868323850 Functional Loss SNV dbSNP153 33..33 33 - - - 92337 RMVar_ID_92337 Human_SNP_ID_518082404 m1A Human chr12 + 120293179 120293179 120293179 TCACGGCGGGGTATTGGGAAAAGTTTTCAATTAGCAATAATCGCGCCTCGGATAGACCTCATTGG TCACGGCGGGGTATTGGGAAAAGTTTTCAATTGGCAATAATCGCGCCTCGGATAGACCTCATTGG A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:120293113..120293208 26863410 MeRIP-seq:(Medium) rs916836386 Functional Loss SNV dbSNP153 33..33 33 - - - 92338 RMVar_ID_92338 Human_SNP_ID_518082405 m1A Human chr12 + 120293179 120293179 120293179 TCACGGCGGGGTATTGGGAAAAGTTTTCAATTAGCAATAATCGCGCCTCGGATAGACCTCATTGG TCACGGCGGGGTATTGGGAAAAGTTTTCAATTTGCAATAATCGCGCCTCGGATAGACCTCATTGG A T RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:120293113..120293208 26863410 MeRIP-seq:(Medium) rs916836386 Functional Loss SNV dbSNP153 33..33 33 - - - 92339 RMVar_ID_92339 Human_SNP_ID_518085709 m1A Human chr12 - 120303580 120303580 120303580 GATCCAACGGCCTTTTGCTGACCTGAAAGTCAACGCAAAGCTCATCTTCATTCTAGAGAAAAAGA GATCCAACGGCCTTTTGCTGACCTGAAAGTCACCGCAAAGCTCATCTTCATTCTAGAGAAAAAGA T G RF00017-049,RF00017-1304,lnc-PLA2G1B-2 RNACentral:URS000096B6E3,RNACentral:URS0000990DE9,RNACentral:URS0000D58AC8 SRP RNA,SRP RNA,lincRNA intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120303575..120303715 26863196 MeRIP-seq:(Medium) rs1202259174 Functional Loss SNV dbSNP153 33..33 33 - - - 92340 RMVar_ID_92340 Human_SNP_ID_518098786 m1A Human chr12 - 120353376 120353376 120353376 CATCTGACACTGCCCCCTTGCCCCATCAGGTTACCCAGGTTTCCAAGCCACAACCTACGCCAGCC CATCTGACACTGCCCCCTTGCCCCATCAGGTTCCCCAGGTTTCCAAGCCACAACCTACGCCAGCC T G MSI1 Ensembl:ENSG00000135097 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120345587..120356960 32194978 MeRIP-seq:(Medium) rs970659874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433000,Human_Splice_Rec_1433001,Human_Splice_Rec_1433022,Human_Splice_Rec_1433023,Human_Splice_Rec_1433034 RMVar_hsa_circ_59497,RMVar_hsa_circ_266395 92341 RMVar_ID_92341 Human_SNP_ID_518102751 m1A Human chr12 + 120369120 120369120 120369120 CCATCGGGAGCCGCGGGCGGCGCGGGCAGCGGAGCGGCGGCGGCGGCGGCGGCGGCGGCGCTCGG CCATCGGGAGCCGCGGGCGGCGCGGGCAGCGGGGCGGCGGCGGCGGCGGCGGCGGCGGCGCTCGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:120369026..120369200 26863410 MeRIP-seq:(Medium) rs1163916509 Functional Loss SNV dbSNP153 33..33 33 - - - 92342 RMVar_ID_92342 Human_SNP_ID_518120638 m1A Human chr12 - 120438145 120438145 120438145 GCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTGATCTGGACT GCGGGACCGACCCAGCAGCCGAGAAACCGAGGTCACACCAACTACCGCCATTTTTGATCTGGACT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120438101..120438450 26863196 MeRIP-seq:(Medium) rs567294603 Functional Loss SNV dbSNP153 33..33 33 - - - 92343 RMVar_ID_92343 Human_SNP_ID_518120639 m1A Human chr12 - 120438145 120438145 120438145 GCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTGATCTGGACT GCGGGACCGACCCAGCAGCCGAGAAACCGAGGGCACACCAACTACCGCCATTTTTGATCTGGACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120438101..120438450 26863196 MeRIP-seq:(Medium) rs567294603 Functional Loss SNV dbSNP153 33..33 33 - - - 92344 RMVar_ID_92344 Human_SNP_ID_518120640 m1A Human chr12 - 120438154 120438146 120438154 CAGCTGTGGGCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTG CAGCTGTGGGCGGGACCGACCCAGCAGCCGAG________GACACACCAACTACCGCCATTTTTG CCTCGGTTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120438101..120438450 26863196 MeRIP-seq:(Medium) rs754588549 Functional Loss DEL dbSNP153 33..40 33 - - - 92345 RMVar_ID_92345 Human_SNP_ID_518120647 m1A Human chr12 - 120438148 120438148 120438148 TGGGCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTGATCTGG TGGGCGGGACCGACCCAGCAGCCGAGAAACCGTGGACACACCAACTACCGCCATTTTTGATCTGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120438101..120438425 26863196 MeRIP-seq:(Medium) rs759197876 Functional Loss SNV dbSNP153 33..33 33 - - - 92346 RMVar_ID_92346 Human_SNP_ID_518120653 m1A Human chr12 - 120438152 120438152 120438152 GCTGTGGGCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTGAT GCTGTGGGCGGGACCGACCCAGCAGCCGAGAACCCGAGGACACACCAACTACCGCCATTTTTGAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120438101..120438391 26863196 MeRIP-seq:(Medium) rs777475898 Functional Loss SNV dbSNP153 33..33 33 - - - 92347 RMVar_ID_92347 Human_SNP_ID_518120655 m1A Human chr12 - 120438154 120438154 120438154 CAGCTGTGGGCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTG CAGCTGTGGGCGGGACCGACCCAGCAGCCGAGCAACCGAGGACACACCAACTACCGCCATTTTTG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120438101..120438450 26863196 MeRIP-seq:(Medium) rs942665096 Functional Loss SNV dbSNP153 33..33 33 - - - 92348 RMVar_ID_92348 Human_SNP_ID_518120764 m1A Human chr12 - 120438385 120438385 120438385 GGAGCGCGACGAAGAAGGTGAGAGTCTTCCACATGCGAGCTGCGGAGAAGCCACAAACGTTCAGC GGAGCGCGACGAAGAAGGTGAGAGTCTTCCACTTGCGAGCTGCGGAGAAGCCACAAACGTTCAGC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:120438101..120438425 26863196 MeRIP-seq:(Medium) rs143732226 Functional Loss SNV dbSNP153 33..33 33 - - - 92349 RMVar_ID_92349 Human_SNP_ID_518120765 m1A Human chr12 - 120438385 120438385 120438385 GGAGCGCGACGAAGAAGGTGAGAGTCTTCCACATGCGAGCTGCGGAGAAGCCACAAACGTTCAGC GGAGCGCGACGAAGAAGGTGAGAGTCTTCCACGTGCGAGCTGCGGAGAAGCCACAAACGTTCAGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:120438101..120438425 26863196 MeRIP-seq:(Medium) rs143732226 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 92350 RMVar_ID_92350 Human_SNP_ID_518123202 m1A Human chr12 - 120446509 120446509 120446509 TGAAGCCCTGGCGCCCGCCCAGAGGGGCCCGAAGGCCCAGCCACACCAACCGCGACCACATTTCT TGAAGCCCTGGCGCCCGCCCAGAGGGGCCCGACGGCCCAGCCACACCAACCGCGACCACATTTCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120446451..120446724 26863196 MeRIP-seq:(Medium) rs1283663576 Functional Loss SNV dbSNP153 33..33 33 - - - 92351 RMVar_ID_92351 Human_SNP_ID_518123306 m1A Human chr12 - 120446712 120446712 120446712 GTCGCGCCACTGCCTCGCGGCTGCCGAAGTCCACAAGCGCTAGACGCTCCAGGTGCTCGATCACC GTCGCGCCACTGCCTCGCGGCTGCCGAAGTCCCCAAGCGCTAGACGCTCCAGGTGCTCGATCACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120446651..120446775 26863196 MeRIP-seq:(Medium) rs1176658145 Functional Loss SNV dbSNP153 33..33 33 - - - 92352 RMVar_ID_92352 Human_SNP_ID_518127395 m1A Human chr12 + 120461213 120461213 120461213 CAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACATATGTGCA CAACTCCTGGGCTCAAGTGATCCTCCCACCTCCGCCTCCTAAGTAACTGGGACTACATATGTGCA A C GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs117232182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_582613,Human_miRNA_ID_1128690 92353 RMVar_ID_92353 Human_SNP_ID_518127396 m1A Human chr12 + 120461213 120461213 120461213 CAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACATATGTGCA CAACTCCTGGGCTCAAGTGATCCTCCCACCTCGGCCTCCTAAGTAACTGGGACTACATATGTGCA A G GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs117232182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_582613,Human_miRNA_ID_1128690 92354 RMVar_ID_92354 Human_SNP_ID_518127628 m1A Human chr12 - 120462157 120462157 120462157 CTCTTTTTGTTTTTGTTTGCATTTCAGGGTGAAACTTCCTACATCCGAGTTTATCCTGAGAGAAG CTCTTTTTGTTTTTGTTTGCATTTCAGGGTGAGACTTCCTACATCCGAGTTTATCCTGAGAGAAG T C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_412414,Human_RBP_ID_1788704,Human_RBP_ID_3395586,Human_RBP_ID_6142345,Human_RBP_ID_17810993,Human_RBP_ID_18188949,Human_RBP_ID_26806229 Human_Splice_Rec_1433090,Human_Splice_Rec_1433092,Human_Splice_Rec_1433100 RMVar_hsa_circ_105111,RMVar_hsa_circ_160784 92355 RMVar_ID_92355 Human_SNP_ID_518128080 m1A Human chr12 - 120464007 120464003 120464008 GATGGAGTGGGGATGGTCGAGTATCTCAGAAAAGAAGACATGGAATATGCCCTGCGTAAACTGGA GATGGAGTGGGGATGGTCGAGTATCTCAGAA_____GACATGGAATATGCCCTGCGTAAACTGGA CTTCTT C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1370157091 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_412436,Human_RBP_ID_1126925,Human_RBP_ID_1465957,Human_RBP_ID_1788714,Human_RBP_ID_4205225,Human_RBP_ID_5437339,Human_RBP_ID_6142426,Human_RBP_ID_8367341,Human_RBP_ID_11842995,Human_RBP_ID_17650502,Human_RBP_ID_17830595,Human_RBP_ID_18619570,Human_RBP_ID_19826110,Human_RBP_ID_22039590,Human_RBP_ID_23542128,Human_RBP_ID_26806230,Human_RBP_ID_26902066,Human_RBP_ID_27210822 Human_Splice_Rec_1433089,Human_Splice_Rec_1433091,Human_Splice_Rec_1433099 92356 RMVar_ID_92356 Human_SNP_ID_518128102 m1A Human chr12 - 120464109 120464109 120464109 TTATGTTCTCCATGCCTAGGACTTCCTCCGTCAGGCAGCTGGCAGGACCTGAAGGATCACATGCG TTATGTTCTCCATGCCTAGGACTTCCTCCGTCGGGCAGCTGGCAGGACCTGAAGGATCACATGCG T C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120464001..120464233 26863196 MeRIP-seq:(Medium) rs533703713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36597,Human_RBP_ID_412441,Human_RBP_ID_1788715,Human_RBP_ID_6142428,Human_RBP_ID_11842995,Human_RBP_ID_17242649,Human_RBP_ID_17650868,Human_RBP_ID_17830596,Human_RBP_ID_19056961,Human_RBP_ID_19728466 Human_Splice_Rec_1433088,Human_Splice_Rec_1433098,Human_Splice_Rec_1433104 92357 RMVar_ID_92357 Human_SNP_ID_518128485 m1A Human chr12 - 120465714 120465714 120465714 ATGGCCAGTGTCGGCTTCGTGTGGAGTTCCCCAGGACTTATGGAGGTCGGGGTGGGTGGCCCCGT ATGGCCAGTGTCGGCTTCGTGTGGAGTTCCCCGGGACTTATGGAGGTCGGGGTGGGTGGCCCCGT T C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120465552..120469725 26863196 MeRIP-seq:(Medium) rs1256559379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412445,Human_RBP_ID_990076,Human_RBP_ID_1465991,Human_RBP_ID_4205232,Human_RBP_ID_5348819,Human_RBP_ID_6142458,Human_RBP_ID_8777003,Human_RBP_ID_9012208,Human_RBP_ID_9279331,Human_RBP_ID_9322749,Human_RBP_ID_11843095,Human_RBP_ID_17650869,Human_RBP_ID_17811015,Human_RBP_ID_22170585,Human_RBP_ID_22793276,Human_RBP_ID_23125180,Human_RBP_ID_23542141,Human_RBP_ID_26322157,Human_RBP_ID_26902077,Human_RBP_ID_27210825,Human_RBP_ID_27623731 Human_Splice_Rec_1433086,Human_Splice_Rec_1433087,Human_Splice_Rec_1433094,Human_Splice_Rec_1433095,Human_Splice_Rec_1433102,Human_Splice_Rec_1433106 92358 RMVar_ID_92358 Human_SNP_ID_518128487 m1A Human chr12 - 120465722 120465722 120465722 TTATGATTATGGCCAGTGTCGGCTTCGTGTGGAGTTCCCCAGGACTTATGGAGGTCGGGGTGGGT TTATGATTATGGCCAGTGTCGGCTTCGTGTGGCGTTCCCCAGGACTTATGGAGGTCGGGGTGGGT T G SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120465546..120469725 26863196 MeRIP-seq:(Medium) rs1485838742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412446,Human_RBP_ID_990076,Human_RBP_ID_1465992,Human_RBP_ID_5348819,Human_RBP_ID_6142458,Human_RBP_ID_8777003,Human_RBP_ID_9012208,Human_RBP_ID_9279331,Human_RBP_ID_9322749,Human_RBP_ID_11843095,Human_RBP_ID_17650869,Human_RBP_ID_17811015,Human_RBP_ID_22170585,Human_RBP_ID_23125181,Human_RBP_ID_23542141,Human_RBP_ID_26322157,Human_RBP_ID_27210825,Human_RBP_ID_27623731 Human_Splice_Rec_1433086,Human_Splice_Rec_1433087,Human_Splice_Rec_1433094,Human_Splice_Rec_1433095,Human_Splice_Rec_1433102,Human_Splice_Rec_1433106 92359 RMVar_ID_92359 Human_SNP_ID_518129716 m1A Human chr12 - 120469527 120469527 120469527 CGTGGGGAACCTTCCGACCGACGTGCGCGAGAAGGACTTGGAGGACCTGTTCTACAAGTACGGCC CGTGGGGAACCTTCCGACCGACGTGCGCGAGAGGGACTTGGAGGACCTGTTCTACAAGTACGGCC T C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120469476..120469650 32194978 MeRIP-seq:(Medium) rs1250789428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229888,Human_RBP_ID_412453,Human_RBP_ID_990078,Human_RBP_ID_1465994,Human_RBP_ID_1788737,Human_RBP_ID_3395609,Human_RBP_ID_4205234,Human_RBP_ID_6142478,Human_RBP_ID_8367362,Human_RBP_ID_8777005,Human_RBP_ID_8940732,Human_RBP_ID_9322751,Human_RBP_ID_11843197,Human_RBP_ID_17468584,Human_RBP_ID_17650870,Human_RBP_ID_18206247,Human_RBP_ID_18619584,Human_RBP_ID_23125183,Human_RBP_ID_23542150,Human_RBP_ID_26902081,Human_RBP_ID_27210828,Human_RBP_ID_27419108 92360 RMVar_ID_92360 Human_SNP_ID_518129717 m1A Human chr12 - 120469527 120469527 120469527 CGTGGGGAACCTTCCGACCGACGTGCGCGAGAAGGACTTGGAGGACCTGTTCTACAAGTACGGCC CGTGGGGAACCTTCCGACCGACGTGCGCGAGACGGACTTGGAGGACCTGTTCTACAAGTACGGCC T G SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120469476..120469650 32194978 MeRIP-seq:(Medium) rs1250789428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229888,Human_RBP_ID_412453,Human_RBP_ID_990078,Human_RBP_ID_1465994,Human_RBP_ID_1788737,Human_RBP_ID_3395609,Human_RBP_ID_4205234,Human_RBP_ID_6142478,Human_RBP_ID_8367362,Human_RBP_ID_8777005,Human_RBP_ID_8940732,Human_RBP_ID_9322751,Human_RBP_ID_11843197,Human_RBP_ID_17468584,Human_RBP_ID_17650870,Human_RBP_ID_18206247,Human_RBP_ID_18619584,Human_RBP_ID_23125183,Human_RBP_ID_23542150,Human_RBP_ID_26902081,Human_RBP_ID_27210828,Human_RBP_ID_27419108 92361 RMVar_ID_92361 Human_SNP_ID_518129784 m1A Human chr12 + 120469667 120469667 120469667 GCCGCAGCCCACGTCGCCGCCGCCGCCTCAGCACGGGTCCCCCCGCAGCGTCCCCGCGGGCTCCG GCCGCAGCCCACGTCGCCGCCGCCGCCTCAGCCCGGGTCCCCCCGCAGCGTCCCCGCGGGCTCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120465581..120469750 26863196 MeRIP-seq:(Medium) rs1397497686 Functional Loss SNV dbSNP153 33..33 33 - - - 92362 RMVar_ID_92362 Human_SNP_ID_518134647 m1A Human chr12 - 120489551 120489551 120489551 AGTTAGAGGCTATTGCAGCAGTCCAGGTAAGAAGGAATGGTGGCTTGGACAAGGAGGTGGTAGCA AGTTAGAGGCTATTGCAGCAGTCCAGGTAAGACGGAATGGTGGCTTGGACAAGGAGGTGGTAGCA T G NRAV Ensembl:ENSG00000248008 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120489437..120489603 26863196 MeRIP-seq:(Medium) rs1169239233 Functional Loss SNV dbSNP153 33..33 33 - - - 92363 RMVar_ID_92363 Human_SNP_ID_518136229 m1A Human chr12 - 120496174 120496173 120496174 GGGGCTGGCCGACTGCAACGGTCTCCTGGGGGAGGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT GGGGCTGGCCGACTGCAACGGTCTCCTGGGGG_GGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr12:120496126..120496200;chr12:120496126..120496225 26863196,32194978 MeRIP-seq:(Medium) rs1230424714 Functional Loss DEL dbSNP153 33..33 33 - - - 92364 RMVar_ID_92364 Human_SNP_ID_518136231 m1A Human chr12 - 120496174 120496174 120496174 GGGGCTGGCCGACTGCAACGGTCTCCTGGGGGAGGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT GGGGCTGGCCGACTGCAACGGTCTCCTGGGGGGGGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr12:120496126..120496200;chr12:120496126..120496225 26863196,32194978 MeRIP-seq:(Medium) rs580016 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12069,GWAS_ID_12070,GWAS_ID_12071,GWAS_ID_12072,GWAS_ID_12073,GWAS_ID_12074,GWAS_ID_12075,GWAS_ID_12076,GWAS_ID_12077,GWAS_ID_12078,GWAS_ID_12079,GWAS_ID_12080,GWAS_ID_12081,GWAS_ID_12082,GWAS_ID_12083,GWAS_ID_12084,GWAS_ID_12085,GWAS_ID_12086 92365 RMVar_ID_92365 Human_SNP_ID_518136367 m1A Human chr12 - 120496471 120496470 120496472 CCTGAGTAGCGCACTCCACCGAGTCCTGTTGCATCTCTTCCGACATGTCCGCATTTTTGATCACG CCTGAGTAGCGCACTCCACCGAGTCCTGTTG__TCTCTTCCGACATGTCCGCATTTTTGATCACG ATG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120496358..120496476 26863196 MeRIP-seq:(Medium) rs1393054729 Functional Loss DEL dbSNP153 32..33 33 - - - 92366 RMVar_ID_92366 Human_SNP_ID_518136368 m1A Human chr12 - 120496471 120496471 120496471 CCTGAGTAGCGCACTCCACCGAGTCCTGTTGCATCTCTTCCGACATGTCCGCATTTTTGATCACG CCTGAGTAGCGCACTCCACCGAGTCCTGTTGCGTCTCTTCCGACATGTCCGCATTTTTGATCACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120496358..120496476 26863196 MeRIP-seq:(Medium) rs751780551 Functional Loss SNV dbSNP153 33..33 33 - - - 92367 RMVar_ID_92367 Human_SNP_ID_518136377 m1A Human chr12 - 120496496 120496496 120496496 TTCTCTATGTTGTATTTCTCCAGCGCCTGAGTAGCGCACTCCACCGAGTCCTGTTGCATCTCTTC TTCTCTATGTTGTATTTCTCCAGCGCCTGAGTCGCGCACTCCACCGAGTCCTGTTGCATCTCTTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr12:120496356..120496496;chr12:120496401..120496575 26863196,32194978 MeRIP-seq:(Medium) rs796364245 Functional Loss SNV dbSNP153 33..33 33 - - - 92368 RMVar_ID_92368 Human_SNP_ID_518138359 m1A Human chr12 - 120503816 120503816 120503816 ACAAGGTGACTTACGAAAGTCTAACATCAGGCATTGTGGCCATTCATTCTGGCTTCAAACTTTAA ACAAGGTGACTTACGAAAGTCTAACATCAGGCGTTGTGGCCATTCATTCTGGCTTCAAACTTTAA T C COQ5 Ensembl:ENSG00000110871 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120503768..120504961 32194978 MeRIP-seq:(Medium) rs138832185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1466020 Human_Splice_Rec_1433164,Human_Splice_Rec_1433174 RMVar_hsa_circ_87522,RMVar_hsa_circ_160791 92369 RMVar_ID_92369 Human_SNP_ID_518141538 m1A Human chr12 + 120516656 120516656 120516656 TGATGTCACACACCACGACACGAGACCCGCCCAAGGAATCTTCTTCATTCTGGTACTCTTTGGCA TGATGTCACACACCACGACACGAGACCCGCCCCAGGAATCTTCTTCATTCTGGTACTCTTTGGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120516605..120516724 26863196 MeRIP-seq:(Medium) rs190556242 Functional Loss SNV dbSNP153 33..33 33 - - - 92370 RMVar_ID_92370 Human_SNP_ID_518141539 m1A Human chr12 + 120516656 120516656 120516656 TGATGTCACACACCACGACACGAGACCCGCCCAAGGAATCTTCTTCATTCTGGTACTCTTTGGCA TGATGTCACACACCACGACACGAGACCCGCCCGAGGAATCTTCTTCATTCTGGTACTCTTTGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120516605..120516724 26863196 MeRIP-seq:(Medium) rs190556242 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 92371 RMVar_ID_92371 Human_SNP_ID_518145219 m1A Human chr12 - 120529002 120529002 120529002 CCTACTAAGTGCTCGGCTCTTGTCCCAAGAGAAGCGGGCAGCGGAAACGCACTTTGGGTTTGAGA CCTACTAAGTGCTCGGCTCTTGTCCCAAGAGAGGCGGGCAGCGGAAACGCACTTTGGGTTTGAGA T C COQ5 Ensembl:ENSG00000110871 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120528951..120529100 32194978 MeRIP-seq:(Medium) rs377206577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412489,Human_RBP_ID_4247059 Human_Splice_Rec_1433153,Human_Splice_Rec_1433165,Human_Splice_Rec_1433175,Human_Splice_Rec_1433189,Human_Splice_Rec_1433199,Human_Splice_Rec_1433205 92372 RMVar_ID_92372 Human_SNP_ID_518145248 m1A Human chr12 + 120529062 120529060 120529062 GTAGGTCCCCGGGCCAAGAGCTACGAAGCCCGAGGAGCTGGCAGCCCCGCATCGCCCGCGACCAC GTAGGTCCCCGGGCCAAGAGCTACGAAGCCC__GGAGCTGGCAGCCCCGCATCGCCCGCGACCAC CGA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120529011..120529111 32194978 MeRIP-seq:(Medium) rs764373282 Functional Loss DEL dbSNP153 32..33 33 - - - 92373 RMVar_ID_92373 Human_SNP_ID_518146767 m1A Human chr12 + 120534726 120534726 120534726 GCCATGAAGGCCGAGAACCGCTGCCGCCGCCGACCCCCGCCGGCCCTGAACGCCATGAGCCTGGG GCCATGAAGGCCGAGAACCGCTGCCGCCGCCGCCCCCCGCCGGCCCTGAACGCCATGAGCCTGGG A C RNF10 Ensembl:ENSG00000022840 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr12:120534409..120534925;chr12:120534676..120534975 26863196 MeRIP-seq:(Medium) rs1057080299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809419,Human_RBP_ID_11843369,Human_RBP_ID_22532445,Human_RBP_ID_27419147 Human_Splice_Rec_1433208 Human_miRNA_ID_2146829,Human_miRNA_ID_2353791,Human_miRNA_ID_2573833,Human_miRNA_ID_2988257,Human_miRNA_ID_3021956 RMVar_hsa_circ_106714,RMVar_hsa_circ_160797 92374 RMVar_ID_92374 Human_SNP_ID_518149958 m1A Human chr12 - 120546421 120546421 120546421 AGTTCACGTTTGCGATTATAACGCTTGGATCCACTGGAGTTCTTTCCATCTGAAAGCAAGAAACA AGTTCACGTTTGCGATTATAACGCTTGGATCCGCTGGAGTTCTTTCCATCTGAAAGCAAGAAACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120546419..120546569 32194978 MeRIP-seq:(Medium) rs1218038438 Functional Loss SNV dbSNP153 33..33 33 - - - 92375 RMVar_ID_92375 Human_SNP_ID_518154771 m1A Human chr12 + 120562908 120562908 120562908 CCTTGCCCTTCAAGCTAAGTGTGTGTCTGGAAACTTAACCTTCTCTGGTGTTCTCTCTGGCCACG CCTTGCCCTTCAAGCTAAGTGTGTGTCTGGAAGCTTAACCTTCTCTGGTGTTCTCTCTGGCCACG A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120562905..120563043 26863196 MeRIP-seq:(Medium) rs771214352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11843890,Human_RBP_ID_23542256 RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_265128,RMVar_hsa_circ_68570,RMVar_hsa_circ_88407,RMVar_hsa_circ_107504,RMVar_hsa_circ_86391,RMVar_hsa_circ_6872,RMVar_hsa_circ_305382,RMVar_hsa_circ_160802,RMVar_hsa_circ_160804,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_290831,RMVar_hsa_circ_294043,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160807,RMVar_hsa_circ_160809,RMVar_hsa_circ_160810,RMVar_hsa_circ_160808,RMVar_hsa_circ_368189,RMVar_hsa_circ_375920,RMVar_hsa_circ_359541,RMVar_hsa_circ_308441,RMVar_hsa_circ_160814,RMVar_hsa_circ_160815,RMVar_hsa_circ_160813,RMVar_hsa_circ_160821,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_354368,RMVar_hsa_circ_80028,RMVar_hsa_circ_160817,RMVar_hsa_circ_160818,RMVar_hsa_circ_160823,RMVar_hsa_circ_309460,RMVar_hsa_circ_370437,RMVar_hsa_circ_300609,RMVar_hsa_circ_160822 92376 RMVar_ID_92376 Human_SNP_ID_518154772 m1A Human chr12 + 120562908 120562908 120562908 CCTTGCCCTTCAAGCTAAGTGTGTGTCTGGAAACTTAACCTTCTCTGGTGTTCTCTCTGGCCACG CCTTGCCCTTCAAGCTAAGTGTGTGTCTGGAATCTTAACCTTCTCTGGTGTTCTCTCTGGCCACG A T RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120562905..120563043 26863196 MeRIP-seq:(Medium) rs771214352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11843890,Human_RBP_ID_23542256 RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_265128,RMVar_hsa_circ_68570,RMVar_hsa_circ_88407,RMVar_hsa_circ_107504,RMVar_hsa_circ_86391,RMVar_hsa_circ_6872,RMVar_hsa_circ_305382,RMVar_hsa_circ_160802,RMVar_hsa_circ_160804,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_290831,RMVar_hsa_circ_294043,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160807,RMVar_hsa_circ_160809,RMVar_hsa_circ_160810,RMVar_hsa_circ_160808,RMVar_hsa_circ_368189,RMVar_hsa_circ_375920,RMVar_hsa_circ_359541,RMVar_hsa_circ_308441,RMVar_hsa_circ_160814,RMVar_hsa_circ_160815,RMVar_hsa_circ_160813,RMVar_hsa_circ_160821,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_354368,RMVar_hsa_circ_80028,RMVar_hsa_circ_160817,RMVar_hsa_circ_160818,RMVar_hsa_circ_160823,RMVar_hsa_circ_309460,RMVar_hsa_circ_370437,RMVar_hsa_circ_300609,RMVar_hsa_circ_160822 92377 RMVar_ID_92377 Human_SNP_ID_518159579 m1A Human chr12 - 120579919 120579919 120579919 CCAAAATGATTTTTCTTTCCTGTTGTAGTTCGATATCTCAATGCCTATACTGGAATAGTGCTACT CCAAAATGATTTTTCTTTCCTGTTGTAGTTCGGTATCTCAATGCCTATACTGGAATAGTGCTACT T C POP5 Ensembl:ENSG00000167272 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120579800..120579949 32194978 MeRIP-seq:(Medium) rs780252851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11844303 Human_Splice_Rec_1433430,Human_Splice_Rec_1433436,Human_Splice_Rec_1433444,Human_Splice_Rec_1433452 RMVar_hsa_circ_88505,RMVar_hsa_circ_90543,RMVar_hsa_circ_160834,RMVar_hsa_circ_160835 92378 RMVar_ID_92378 Human_SNP_ID_518186446 m1A Human chr12 + 120687502 120687502 120687502 GCATGTGGACGTGCACGGGATCCACTTCCGCAAGGACCCTTTGGAAGGCCGGGTGGGCCGAGGTG GCATGTGGACGTGCACGGGATCCACTTCCGCAGGGACCCTTTGGAAGGCCGGGTGGGCCGAGGTG A G MLEC Ensembl:ENSG00000110917 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120687151..120687598 26863196 MeRIP-seq:(Medium) rs760226011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412559,Human_RBP_ID_873922,Human_RBP_ID_1466080,Human_RBP_ID_4247922,Human_RBP_ID_6142803,Human_RBP_ID_9352852,Human_RBP_ID_17112400,Human_RBP_ID_22437485,Human_RBP_ID_22910807 Human_Splice_Rec_1433511,Human_Splice_Rec_1433519 RMVar_hsa_circ_128145,RMVar_hsa_circ_160837,RMVar_hsa_circ_77514,RMVar_hsa_circ_160836 92379 RMVar_ID_92379 Human_SNP_ID_518188154 m1A Human chr12 + 120694984 120694984 120694984 GGGGGAGGTGTCCACCTTCACAGGGAAACTCTACATTGAGTTTGTCAAGGTAATTCCCCTATTCT GGGGGAGGTGTCCACCTTCACAGGGAAACTCTCCATTGAGTTTGTCAAGGTAATTCCCCTATTCT A C MLEC Ensembl:ENSG00000110917 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120694826..120695025 32194978 MeRIP-seq:(Medium) rs1212997458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059438,Human_RBP_ID_22492482 Human_Splice_Rec_1433515,Human_Splice_Rec_1433525,Human_Splice_Rec_1433531 RMVar_hsa_circ_80500,RMVar_hsa_circ_128145,RMVar_hsa_circ_160837,RMVar_hsa_circ_77514,RMVar_hsa_circ_160836,RMVar_hsa_circ_96742,RMVar_hsa_circ_160839,RMVar_hsa_circ_160840 92380 RMVar_ID_92380 Human_SNP_ID_518188155 m1A Human chr12 + 120694984 120694984 120694984 GGGGGAGGTGTCCACCTTCACAGGGAAACTCTACATTGAGTTTGTCAAGGTAATTCCCCTATTCT GGGGGAGGTGTCCACCTTCACAGGGAAACTCTGCATTGAGTTTGTCAAGGTAATTCCCCTATTCT A G MLEC Ensembl:ENSG00000110917 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120694826..120695025 32194978 MeRIP-seq:(Medium) rs1212997458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059438,Human_RBP_ID_22492482 Human_Splice_Rec_1433515,Human_Splice_Rec_1433525,Human_Splice_Rec_1433531 RMVar_hsa_circ_80500,RMVar_hsa_circ_128145,RMVar_hsa_circ_160837,RMVar_hsa_circ_77514,RMVar_hsa_circ_160836,RMVar_hsa_circ_96742,RMVar_hsa_circ_160839,RMVar_hsa_circ_160840 92381 RMVar_ID_92381 Human_SNP_ID_518188201 m1A Human chr12 - 120695154 120695154 120695154 TCAAGTCAAAAAAGCAGGTCAGAACACAACCTACCATCCACTGTCCCAGCCATGATGTAGAGTGC TCAAGTCAAAAAAGCAGGTCAGAACACAACCTCCCATCCACTGTCCCAGCCATGATGTAGAGTGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120695076..120695175 32194978 MeRIP-seq:(Medium) rs774308113 Functional Loss SNV dbSNP153 33..33 33 - - - 92382 RMVar_ID_92382 Human_SNP_ID_518188470 m1A Human chr12 + 120696418 120696418 120696418 TGAAGGGTCTAATCTCAAAAAACAGACCAATAAGAACCGGGTGCAGTCAGGCCCCCGCACACCCA TGAAGGGTCTAATCTCAAAAAACAGACCAATAGGAACCGGGTGCAGTCAGGCCCCCGCACACCCA A G MLEC Ensembl:ENSG00000110917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120696368..120696487 26863196 MeRIP-seq:(Medium) rs1313248155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_412571,Human_RBP_ID_753206,Human_RBP_ID_878905,Human_RBP_ID_9365702,Human_RBP_ID_23113411,Human_RBP_ID_24543506,Human_RBP_ID_26322161,Human_RBP_ID_26412808,Human_RBP_ID_27557695 Human_miRNA_ID_3002700 RMVar_hsa_circ_80500,RMVar_hsa_circ_160837,RMVar_hsa_circ_77514,RMVar_hsa_circ_112729,RMVar_hsa_circ_96742,RMVar_hsa_circ_160839,RMVar_hsa_circ_160840,RMVar_hsa_circ_160841 92383 RMVar_ID_92383 Human_SNP_ID_518188529 m1A Human chr12 - 120696602 120696602 120696602 TAATCATTGTGAAAAATACAGAAACCAAAACCAATATGGCTGGTTTCTTTCCCACACCCCTCCAC TAATCATTGTGAAAAATACAGAAACCAAAACCTATATGGCTGGTTTCTTTCCCACACCCCTCCAC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120696551..120696675 32194978 MeRIP-seq:(Medium) rs1456383076 Functional Loss SNV dbSNP153 33..33 33 - - - 92384 RMVar_ID_92384 Human_SNP_ID_518189063 m1A Human chr12 - 120699324 120699324 120699324 GGATCTAAAAACCTGGGACAGAGTGTAGATCCAGTAGAGGAGCCCAGGCCTCTCCTCCACGCACC GGATCTAAAAACCTGGGACAGAGTGTAGATCCGGTAGAGGAGCCCAGGCCTCTCCTCCACGCACC T C AC069234.2 Ensembl:ENSG00000256364 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:120699301..120699325 32194978 MeRIP-seq:(Medium) rs1196536166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433535 92385 RMVar_ID_92385 Human_SNP_ID_518189310 m1A Human chr12 + 120700550 120700550 120700550 GACTGAGGCAAGGCAAAGTGATAGTACACGGAAGCAGAACCGGAAACACCCAGGAACTGTTCAGA GACTGAGGCAAGGCAAAGTGATAGTACACGGAGGCAGAACCGGAAACACCCAGGAACTGTTCAGA A G MLEC Ensembl:ENSG00000110917 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120700501..120700600 32194978 MeRIP-seq:(Medium) rs952814132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5174049,Human_RBP_ID_17683563,Human_RBP_ID_19701874,Human_RBP_ID_26412918,Human_RBP_ID_27419203 Human_Splice_Rec_1433534 Human_miRNA_ID_2668871,Human_miRNA_ID_3002701,Human_miRNA_ID_3019385 RMVar_hsa_circ_80500,RMVar_hsa_circ_160837,RMVar_hsa_circ_77514,RMVar_hsa_circ_112729,RMVar_hsa_circ_96742,RMVar_hsa_circ_160839,RMVar_hsa_circ_160840,RMVar_hsa_circ_160841 92386 RMVar_ID_92386 Human_SNP_ID_518191733 m1A Human chr12 + 120710676 120710676 120710676 TCACGGAGCAGGAGCTGCTGGCGCTGGACACCATCCGGCCCGAGCACGTCCTGCGCCTCAGCCGG TCACGGAGCAGGAGCTGCTGGCGCTGGACACCCTCCGGCCCGAGCACGTCCTGCGCCTCAGCCGG A C UNC119B Ensembl:ENSG00000175970 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:120710476..120710783 26863410 MeRIP-seq:(Medium) rs1473154994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9277160,Human_RBP_ID_22492487 Human_Splice_Rec_1433539,Human_Splice_Rec_1433547 RMVar_hsa_circ_117258,RMVar_hsa_circ_160843 92387 RMVar_ID_92387 Human_SNP_ID_518191734 m1A Human chr12 + 120710676 120710676 120710676 TCACGGAGCAGGAGCTGCTGGCGCTGGACACCATCCGGCCCGAGCACGTCCTGCGCCTCAGCCGG TCACGGAGCAGGAGCTGCTGGCGCTGGACACCGTCCGGCCCGAGCACGTCCTGCGCCTCAGCCGG A G UNC119B Ensembl:ENSG00000175970 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:120710476..120710783 26863410 MeRIP-seq:(Medium) rs1473154994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9277160,Human_RBP_ID_22492487 Human_Splice_Rec_1433539,Human_Splice_Rec_1433547 RMVar_hsa_circ_117258,RMVar_hsa_circ_160843 92388 RMVar_ID_92388 Human_SNP_ID_518195700 m1A Human chr12 - 120725921 120725921 120725921 TACGGATCCCCAGCGCACTCACCTCTGCGGGCAGGGCCCGAGGCCCGGGCGAGCAGCGCGGCGGC TACGGATCCCCAGCGCACTCACCTCTGCGGGCCGGGCCCGAGGCCCGGGCGAGCAGCGCGGCGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120725871..120725938 26863196 MeRIP-seq:(Medium) rs1204157490 Functional Loss SNV dbSNP153 33..33 33 - - - 92389 RMVar_ID_92389 Human_SNP_ID_518208568 m1A Human chr12 - 120771015 120771014 120771016 AGGATGGCGGCTTAAGCCAGGCAGGGTGTAAAAGAGAGACGGGTCAAAAACGACATCACAGATTT AGGATGGCGGCTTAAGCCAGGCAGGGTGTAA__GAGAGACGGGTCAAAAACGACATCACAGATTT CTT C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120770988..120771086 26863196 MeRIP-seq:(Medium) rs1292813686 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_271105,RMVar_hsa_circ_265688,RMVar_hsa_circ_68822,RMVar_hsa_circ_160855,RMVar_hsa_circ_342598,RMVar_hsa_circ_266422 92390 RMVar_ID_92390 Human_SNP_ID_518208569 m1A Human chr12 - 120771015 120771015 120771015 AGGATGGCGGCTTAAGCCAGGCAGGGTGTAAAAGAGAGACGGGTCAAAAACGACATCACAGATTT AGGATGGCGGCTTAAGCCAGGCAGGGTGTAAAGGAGAGACGGGTCAAAAACGACATCACAGATTT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120770988..120771086 26863196 MeRIP-seq:(Medium) rs1242740044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_271105,RMVar_hsa_circ_265688,RMVar_hsa_circ_68822,RMVar_hsa_circ_160855,RMVar_hsa_circ_342598,RMVar_hsa_circ_266422 92391 RMVar_ID_92391 Human_SNP_ID_518208636 m1A Human chr12 + 120771326 120771326 120771326 CCAGCCACAGCAGCCTCCTCACTCTACCCCCCATGCCGCCGCTTCGGCCACGCCGCCGCTTCAGT CCAGCCACAGCAGCCTCCTCACTCTACCCCCCGTGCCGCCGCTTCGGCCACGCCGCCGCTTCAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120771283..120771479 26863196 MeRIP-seq:(Medium) rs977545164 Functional Loss SNV dbSNP153 33..33 33 - - - 92392 RMVar_ID_92392 Human_SNP_ID_518227547 m1A Human chr12 - 120844456 120844456 120844456 AGGTAGACAGGAGCTTGGGTTTTATCAGCACGATGGGAGGCTGTTAGAGGATTTTAAACAGGCAC AGGTAGACAGGAGCTTGGGTTTTATCAGCACGGTGGGAGGCTGTTAGAGGATTTTAAACAGGCAC T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120844446..120844554 26863196 MeRIP-seq:(Medium) rs1198652271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12075429 RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 92393 RMVar_ID_92393 Human_SNP_ID_518243412 m1A Human chr12 - 120902793 120902793 120902793 GAGAGTGAGGAAGCAAGAAATGGCATGATCGTAGGAGTGGGGGACCTGATTGCAATTTAGAGAAA GAGAGTGAGGAAGCAAGAAATGGCATGATCGTGGGAGTGGGGGACCTGATTGCAATTTAGAGAAA T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120902784..120902951 26863196 MeRIP-seq:(Medium) rs1217003362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 92394 RMVar_ID_92394 Human_SNP_ID_518243871 m1A Human chr12 - 120904128 120904128 120904128 CGCCGCCGCCGCCATGTTGGGTTTGGAGCTGCAGCGGAGCCGCCGCCGCCGCCGCGGGTGAGGGA CGCCGCCGCCGCCATGTTGGGTTTGGAGCTGCGGCGGAGCCGCCGCCGCCGCCGCGGGTGAGGGA T C SPPL3 Ensembl:ENSG00000157837 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120902756..120904375 26863196 MeRIP-seq:(Medium) rs1203591877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229111,Human_RBP_ID_412913,Human_RBP_ID_990186,Human_RBP_ID_1466182,Human_RBP_ID_4246369,Human_RBP_ID_5139961,Human_RBP_ID_5314687,Human_RBP_ID_5347823,Human_RBP_ID_8367571,Human_RBP_ID_9323275,Human_RBP_ID_22039603,Human_RBP_ID_22436737,Human_RBP_ID_22532527,Human_RBP_ID_22573637 Human_miRNA_ID_2013128,Human_miRNA_ID_2759511 RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 92395 RMVar_ID_92395 Human_SNP_ID_518243873 m1A Human chr12 + 120904137 120904137 120904137 CGCGGCGGCGGCGGCGGCTCCGCTGCAGCTCCAAACCCAACATGGCGGCGGCGGCGGCGCGGAGA CGCGGCGGCGGCGGCGGCTCCGCTGCAGCTCCGAACCCAACATGGCGGCGGCGGCGGCGCGGAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:120903249..120904371 26863196 MeRIP-seq:(Medium) rs1377622842 Functional Loss SNV dbSNP153 33..33 33 - - - 92396 RMVar_ID_92396 Human_SNP_ID_518243892 m1A Human chr12 - 120904182 120904182 120904182 AGCGCGGGCCCGTCTTGCCGTTCGCCCGCCCCAGGGCCCCCTTGTTCTCCGCGCCGCCGCCGCCG AGCGCGGGCCCGTCTTGCCGTTCGCCCGCCCCGGGGCCCCCTTGTTCTCCGCGCCGCCGCCGCCG T C SPPL3 Ensembl:ENSG00000157837 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:120903925..120904303 26863196 MeRIP-seq:(Medium) rs1234454602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247074,Human_RBP_ID_5139961,Human_RBP_ID_9322760,Human_RBP_ID_22040125,Human_RBP_ID_22436737 Human_miRNA_ID_2386957,Human_miRNA_ID_2388432,Human_miRNA_ID_2399580,Human_miRNA_ID_3030635 RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 92397 RMVar_ID_92397 Human_SNP_ID_518243929 m1A Human chr12 + 120904290 120904257 120904290 GGCGGCGGCCGGGGGACATGGCCGGCGGGCGGAGGCGGCGGCGACTGAGGGGGGCGCTAGGCGAT _________________________________GGCGGCGGCGACTGAGGGGGGCGCTAGGCGAT CGGCGGCGGCCGGGGGACATGGCCGGCGGGCGGA C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:120904194..120904371 26863410 MeRIP-seq:(Medium) rs1390788332 Functional Loss DEL dbSNP153 1..33 33 - - - 92398 RMVar_ID_92398 Human_SNP_ID_518243948 m1A Human chr12 + 120904290 120904290 120904290 GGCGGCGGCCGGGGGACATGGCCGGCGGGCGGAGGCGGCGGCGACTGAGGGGGGCGCTAGGCGAT GGCGGCGGCCGGGGGACATGGCCGGCGGGCGGGGGCGGCGGCGACTGAGGGGGGCGCTAGGCGAT A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:120904194..120904371 26863410 MeRIP-seq:(Medium) rs1003192880 Functional Loss SNV dbSNP153 33..33 33 - - - 92399 RMVar_ID_92399 Human_SNP_ID_518243951 m1A Human chr12 + 120904301 120904298 120904301 GGGGACATGGCCGGCGGGCGGAGGCGGCGGCGACTGAGGGGGGCGCTAGGCGATGAGGCGAGGCC GGGGACATGGCCGGCGGGCGGAGGCGGCGG___CTGAGGGGGGCGCTAGGCGATGAGGCGAGGCC GCGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120903724..120904350 26863196 MeRIP-seq:(Medium) rs978372765 Functional Loss DEL dbSNP153 31..33 33 - - - 92400 RMVar_ID_92400 Human_SNP_ID_518272053 m1A Human chr12 - 121004256 121004256 121004256 CCAGAAGCAGAAGTCAGGTGAGCTCAACGGGGACCAGGTGTCGCTTGGGACCAAAAAGAAGAAAA CCAGAAGCAGAAGTCAGGTGAGCTCAACGGGGGCCAGGTGTCGCTTGGGACCAAAAAGAAGAAAA T C C12orf43 Ensembl:ENSG00000157895 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121004210..121004352 26863196 MeRIP-seq:(Medium) rs764806741 Functional Loss SNV dbSNP153 33..33 33 - - - 92401 RMVar_ID_92401 Human_SNP_ID_518333559 m1A Human chr12 + 121245329 121245329 121245329 TCTGGGCAACATCCTCCCTCTTCCTTCTCCCCAGCCCCTGCCAGCTCCCAGGGCTGGTGACCGAT TCTGGGCAACATCCTCCCTCTTCCTTCTCCCCCGCCCCTGCCAGCTCCCAGGGCTGGTGACCGAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121245327..121245473 26863196 MeRIP-seq:(Medium) rs1250803324 Functional Loss SNV dbSNP153 33..33 33 - - - 92402 RMVar_ID_92402 Human_SNP_ID_518333974 m1A Human chr12 + 121246994 121246994 121246994 AAGTCAGACCACTTCCCAGTATCTACCCGCCCATCCCTGCTCCAGCTGCCCTGGTTCAAACCCTG AAGTCAGACCACTTCCCAGTATCTACCCGCCCTTCCCTGCTCCAGCTGCCCTGGTTCAAACCCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121246985..121247187 26863196 MeRIP-seq:(Medium) rs1021815331 Functional Loss SNV dbSNP153 33..33 33 - - - 92403 RMVar_ID_92403 Human_SNP_ID_518355113 m1A Human chr12 - 121331425 121331425 121331425 TGGGATATTAATGTTTAGTCTGTCATTAGTCAACAGGCAGAGCTCGCCCTGCAGGAGGCAATTAG TGGGATATTAATGTTTAGTCTGTCATTAGTCAGCAGGCAGAGCTCGCCCTGCAGGAGGCAATTAG T C ANAPC5 Ensembl:ENSG00000089053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:121331326..121331450 32194978 MeRIP-seq:(Medium) rs781824563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11848979,Human_RBP_ID_24940021,Human_RBP_ID_26807258 Human_Splice_Rec_1434856,Human_Splice_Rec_1434857,Human_Splice_Rec_1434876,Human_Splice_Rec_1434877,Human_Splice_Rec_1434896,Human_Splice_Rec_1434897,Human_Splice_Rec_1434926,Human_Splice_Rec_1434927,Human_Splice_Rec_1434984,Human_Splice_Rec_1434985,Human_Splice_Rec_1435040,Human_Splice_Rec_1435041,Human_Splice_Rec_1435064,Human_Splice_Rec_1435065,Human_Splice_Rec_1435086 RMVar_hsa_circ_111714,RMVar_hsa_circ_13766,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_332271,RMVar_hsa_circ_76171,RMVar_hsa_circ_160908,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 92404 RMVar_ID_92404 Human_SNP_ID_518356496 m1A Human chr12 - 121337584 121337584 121337584 AAGAGGAAACAGTGTTGTAGATGGTCAAGAGGAGAGCATGTGGCAGGGTCCACCTTCAGTGTTAC AAGAGGAAACAGTGTTGTAGATGGTCAAGAGGGGAGCATGTGGCAGGGTCCACCTTCAGTGTTAC T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121337582..121337672 26863196 MeRIP-seq:(Medium) rs1555273636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11849237 RMVar_hsa_circ_111714,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_313313,RMVar_hsa_circ_358407,RMVar_hsa_circ_76171,RMVar_hsa_circ_3941,RMVar_hsa_circ_86554,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905,RMVar_hsa_circ_270470,RMVar_hsa_circ_311975,RMVar_hsa_circ_356730,RMVar_hsa_circ_160912,RMVar_hsa_circ_160913,RMVar_hsa_circ_160914,RMVar_hsa_circ_63098 92405 RMVar_ID_92405 Human_SNP_ID_518358532 m1A Human chr12 + 121345907 121345907 121345907 CTTTCACCCTCATCTCTACTGGTCAGTTCCATATCAGCATCCTCCACTGTCTTTTTCTCACCATT CTTTCACCCTCATCTCTACTGGTCAGTTCCATGTCAGCATCCTCCACTGTCTTTTTCTCACCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121345826..121345950 26863196 MeRIP-seq:(Medium) rs566792082 Functional Loss SNV dbSNP153 33..33 33 - - - 92406 RMVar_ID_92406 Human_SNP_ID_518358533 m1A Human chr12 - 121345908 121345908 121345908 GAATGGTGAGAAAAAGACAGTGGAGGATGCTGATATGGAACTGACCAGTAGAGATGAGGGTGAAA GAATGGTGAGAAAAAGACAGTGGAGGATGCTGTTATGGAACTGACCAGTAGAGATGAGGGTGAAA T A ANAPC5 Ensembl:ENSG00000089053 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121345810..121345975 26863196 MeRIP-seq:(Medium) rs782540524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1789036,Human_RBP_ID_3943675,Human_RBP_ID_4206423,Human_RBP_ID_8367663,Human_RBP_ID_8777248,Human_RBP_ID_11849373,Human_RBP_ID_17468694,Human_RBP_ID_18976352,Human_RBP_ID_22793311,Human_RBP_ID_23542964,Human_RBP_ID_26322167 Human_Splice_Rec_1434849,Human_Splice_Rec_1434919,Human_Splice_Rec_1434949,Human_Splice_Rec_1434977,Human_Splice_Rec_1435093,Human_Splice_Rec_1435103,Human_Splice_Rec_1435116 Human_miRNA_ID_2245603 RMVar_hsa_circ_111714,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_313313,RMVar_hsa_circ_358407,RMVar_hsa_circ_3941,RMVar_hsa_circ_36437,RMVar_hsa_circ_270470,RMVar_hsa_circ_311975,RMVar_hsa_circ_356730,RMVar_hsa_circ_160913,RMVar_hsa_circ_160914,RMVar_hsa_circ_63098,RMVar_hsa_circ_72271,RMVar_hsa_circ_106943,RMVar_hsa_circ_332100,RMVar_hsa_circ_160915 92407 RMVar_ID_92407 Human_SNP_ID_518358534 m1A Human chr12 - 121345908 121345908 121345908 GAATGGTGAGAAAAAGACAGTGGAGGATGCTGATATGGAACTGACCAGTAGAGATGAGGGTGAAA GAATGGTGAGAAAAAGACAGTGGAGGATGCTGGTATGGAACTGACCAGTAGAGATGAGGGTGAAA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121345810..121345975 26863196 MeRIP-seq:(Medium) rs782540524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1789036,Human_RBP_ID_3943675,Human_RBP_ID_4206423,Human_RBP_ID_8367663,Human_RBP_ID_8777248,Human_RBP_ID_11849373,Human_RBP_ID_17468694,Human_RBP_ID_18976352,Human_RBP_ID_22793311,Human_RBP_ID_23542964,Human_RBP_ID_26322167 Human_Splice_Rec_1434849,Human_Splice_Rec_1434919,Human_Splice_Rec_1434949,Human_Splice_Rec_1434977,Human_Splice_Rec_1435093,Human_Splice_Rec_1435103,Human_Splice_Rec_1435116 Human_miRNA_ID_2245603 RMVar_hsa_circ_111714,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_313313,RMVar_hsa_circ_358407,RMVar_hsa_circ_3941,RMVar_hsa_circ_36437,RMVar_hsa_circ_270470,RMVar_hsa_circ_311975,RMVar_hsa_circ_356730,RMVar_hsa_circ_160913,RMVar_hsa_circ_160914,RMVar_hsa_circ_63098,RMVar_hsa_circ_72271,RMVar_hsa_circ_106943,RMVar_hsa_circ_332100,RMVar_hsa_circ_160915 92408 RMVar_ID_92408 Human_SNP_ID_518358535 m1A Human chr12 - 121345908 121345908 121345908 GAATGGTGAGAAAAAGACAGTGGAGGATGCTGATATGGAACTGACCAGTAGAGATGAGGGTGAAA GAATGGTGAGAAAAAGACAGTGGAGGATGCTGCTATGGAACTGACCAGTAGAGATGAGGGTGAAA T G ANAPC5 Ensembl:ENSG00000089053 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121345810..121345975 26863196 MeRIP-seq:(Medium) rs782540524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1789036,Human_RBP_ID_3943675,Human_RBP_ID_4206423,Human_RBP_ID_8367663,Human_RBP_ID_8777248,Human_RBP_ID_11849373,Human_RBP_ID_17468694,Human_RBP_ID_18976352,Human_RBP_ID_22793311,Human_RBP_ID_23542964,Human_RBP_ID_26322167 Human_Splice_Rec_1434849,Human_Splice_Rec_1434919,Human_Splice_Rec_1434949,Human_Splice_Rec_1434977,Human_Splice_Rec_1435093,Human_Splice_Rec_1435103,Human_Splice_Rec_1435116 Human_miRNA_ID_2245603 RMVar_hsa_circ_111714,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_313313,RMVar_hsa_circ_358407,RMVar_hsa_circ_3941,RMVar_hsa_circ_36437,RMVar_hsa_circ_270470,RMVar_hsa_circ_311975,RMVar_hsa_circ_356730,RMVar_hsa_circ_160913,RMVar_hsa_circ_160914,RMVar_hsa_circ_63098,RMVar_hsa_circ_72271,RMVar_hsa_circ_106943,RMVar_hsa_circ_332100,RMVar_hsa_circ_160915 92409 RMVar_ID_92409 Human_SNP_ID_518360143 m1A Human chr12 + 121352352 121352344 121352353 GCTCTCGTGGACGCTGGCCATGGCGGCCCGAGACTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA GCTCTCGTGGACGCTGGCCATGGCG_________TAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA GGCCCGAGAC G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:121352251..121352425 26863410 MeRIP-seq:(Medium) rs1555275521 Functional Loss DEL dbSNP153 26..34 33 - - - 92410 RMVar_ID_92410 Human_SNP_ID_518360145 m1A Human chr12 + 121352352 121352346 121352352 GCTCTCGTGGACGCTGGCCATGGCGGCCCGAGACTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA GCTCTCGTGGACGCTGGCCATGGCGGC______CTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA CCCGAGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:121352251..121352425 26863410 MeRIP-seq:(Medium) rs781872789 Functional Loss DEL dbSNP153 28..33 33 - - - 92411 RMVar_ID_92411 Human_SNP_ID_518360160 m1A Human chr12 + 121352352 121352352 121352352 GCTCTCGTGGACGCTGGCCATGGCGGCCCGAGACTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA GCTCTCGTGGACGCTGGCCATGGCGGCCCGAGGCTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:121352251..121352425 26863410 MeRIP-seq:(Medium) rs1555275530 Functional Loss SNV dbSNP153 33..33 33 - - - 92412 RMVar_ID_92412 Human_SNP_ID_518360212 m1A Human chr12 + 121352384 121352384 121352384 ACTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCAGTTGTCACCACAAGGCACAACACTACCGGGTC ACTAAGTCTCGGGCCCGCGGCGCGCTGCCGCCCGTTGTCACCACAAGGCACAACACTACCGGGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121352190..121352450 26863196 MeRIP-seq:(Medium) rs782691156 Functional Loss SNV dbSNP153 33..33 33 - - - 92413 RMVar_ID_92413 Human_SNP_ID_518374202 m1A Human chr12 + 121399803 121399803 121399803 AAACTTGACCACCTAGCCCAGAAAGCCGCAGCAGCTTCCTCAGGGACGCTATCTCCCATTTCAAA AAACTTGACCACCTAGCCCAGAAAGCCGCAGCGGCTTCCTCAGGGACGCTATCTCCCATTTCAAA A G AC048337.1 Ensembl:ENSG00000258435 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121399753..121399836 26863196 MeRIP-seq:(Medium) rs1302463062 Functional Loss SNV dbSNP153 33..33 33 - - - 92414 RMVar_ID_92414 Human_SNP_ID_518374414 m1A Human chr12 - 121400179 121400178 121400179 GCCGCGACCGCCTCAGCTCGGCCGGCTCTACCAGGAAACTCAGCACCATAGCAGCTCCTCACACT GCCGCGACCGCCTCAGCTCGGCCGGCTCTACC_GGAAACTCAGCACCATAGCAGCTCCTCACACT CT C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121400126..121400418 26863196 MeRIP-seq:(Medium) rs782717878 Functional Loss DEL dbSNP153 33..33 33 - - - 92415 RMVar_ID_92415 Human_SNP_ID_518374415 m1A Human chr12 - 121400179 121400179 121400179 GCCGCGACCGCCTCAGCTCGGCCGGCTCTACCAGGAAACTCAGCACCATAGCAGCTCCTCACACT GCCGCGACCGCCTCAGCTCGGCCGGCTCTACCGGGAAACTCAGCACCATAGCAGCTCCTCACACT T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121400126..121400418 26863196 MeRIP-seq:(Medium) rs781843715 Functional Loss SNV dbSNP153 33..33 33 - - - 92416 RMVar_ID_92416 Human_SNP_ID_518374418 m1A Human chr12 - 121400182 121400182 121400182 ATGGCCGCGACCGCCTCAGCTCGGCCGGCTCTACCAGGAAACTCAGCACCATAGCAGCTCCTCAC ATGGCCGCGACCGCCTCAGCTCGGCCGGCTCTGCCAGGAAACTCAGCACCATAGCAGCTCCTCAC T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121400126..121400261 26863196 MeRIP-seq:(Medium) rs782440713 Functional Loss SNV dbSNP153 33..33 33 - - - 92417 RMVar_ID_92417 Human_SNP_ID_518374419 m1A Human chr12 - 121400182 121400182 121400182 ATGGCCGCGACCGCCTCAGCTCGGCCGGCTCTACCAGGAAACTCAGCACCATAGCAGCTCCTCAC ATGGCCGCGACCGCCTCAGCTCGGCCGGCTCTCCCAGGAAACTCAGCACCATAGCAGCTCCTCAC T G lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121400126..121400261 26863196 MeRIP-seq:(Medium) rs782440713 Functional Loss SNV dbSNP153 33..33 33 - - - 92418 RMVar_ID_92418 Human_SNP_ID_518378533 m1A Human chr12 + 121416369 121416369 121416369 GTAAAGCCTGTGGGCTTTCATTTTCAGTCTTTAGAAAGAAGGTGAGTTGGATGAAATGTTACATA GTAAAGCCTGTGGGCTTTCATTTTCAGTCTTTGGAAAGAAGGTGAGTTGGATGAAATGTTACATA A G RNF34 Ensembl:ENSG00000170633 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:121416319..121416420 32194978 MeRIP-seq:(Medium) rs1555282200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2309391,Human_RBP_ID_6144232 Human_Splice_Rec_1435137,Human_Splice_Rec_1435157,Human_Splice_Rec_1435171,Human_Splice_Rec_1435179,Human_Splice_Rec_1435183,Human_Splice_Rec_1435197 RMVar_hsa_circ_42823,RMVar_hsa_circ_273207,RMVar_hsa_circ_160918,RMVar_hsa_circ_288450,RMVar_hsa_circ_160916,RMVar_hsa_circ_339653,RMVar_hsa_circ_280713,RMVar_hsa_circ_160917 92419 RMVar_ID_92419 Human_SNP_ID_518392409 m1A Human chr12 - 121466973 121466963 121466974 GAGCGGGGCGTAGAGGAGCGCGGCAGGCCCGCAGCCGGCCCGGGCAGGGGGCGTGTGCGGCCGAG GAGCGGGGCGTAGAGGAGCGCGGCAGGCCCG___________GGCAGGGGGCGTGTGCGGCCGAG CCGGGCCGGCTG C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121466961..121467141 26863196 MeRIP-seq:(Medium) rs1388831105 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_468,RMVar_hsa_circ_47992,RMVar_hsa_circ_101784,RMVar_hsa_circ_160923,RMVar_hsa_circ_94276,RMVar_hsa_circ_103737,RMVar_hsa_circ_160922,RMVar_hsa_circ_160924,RMVar_hsa_circ_348249,RMVar_hsa_circ_333954,RMVar_hsa_circ_21309 92420 RMVar_ID_92420 Human_SNP_ID_518392530 m1A Human chr12 + 121467254 121467254 121467254 GGGCCCAGGCTCGCGCGCGCTGACATGGCTGGAGCGGCGCCGCCGCCGCCGCCCGCCCGGAGCAG GGGCCCAGGCTCGCGCGCGCTGACATGGCTGGGGCGGCGCCGCCGCCGCCGCCCGCCCGGAGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:121467225..121467337;chr12:121467221..121467320 26863196 MeRIP-seq:(Medium) rs1406539766 Functional Loss SNV dbSNP153 33..33 33 - - - 92421 RMVar_ID_92421 Human_SNP_ID_518392531 m1A Human chr12 + 121467254 121467254 121467254 GGGCCCAGGCTCGCGCGCGCTGACATGGCTGGAGCGGCGCCGCCGCCGCCGCCCGCCCGGAGCAG GGGCCCAGGCTCGCGCGCGCTGACATGGCTGGTGCGGCGCCGCCGCCGCCGCCCGCCCGGAGCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:121467225..121467337;chr12:121467221..121467320 26863196 MeRIP-seq:(Medium) rs1406539766 Functional Loss SNV dbSNP153 33..33 33 - - - 92422 RMVar_ID_92422 Human_SNP_ID_518410920 m1A Human chr12 - 121537246 121537246 121537246 GAGCAAACCAGCCAGGGGGGAGCCCCGGAGCCAGCGCGGGGCGGGAGCGGGGGTGGCCTGTCGCT GAGCAAACCAGCCAGGGGGGAGCCCCGGAGCCGGCGCGGGGCGGGAGCGGGGGTGGCCTGTCGCT T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121537239..121537549 26863196 MeRIP-seq:(Medium) rs1315703447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_10764,RMVar_hsa_circ_309099,RMVar_hsa_circ_20833,RMVar_hsa_circ_15469,RMVar_hsa_circ_325352,RMVar_hsa_circ_14388,RMVar_hsa_circ_160928,RMVar_hsa_circ_302455,RMVar_hsa_circ_336377 92423 RMVar_ID_92423 Human_SNP_ID_518410969 m1A Human chr12 + 121537395 121537395 121537395 GGTGCCACGGCCGCTAAGCTCTCCCCACGGCCAGCCGGCTAGCCCGGCTTCCGCCTGGGCCTCGG GGTGCCACGGCCGCTAAGCTCTCCCCACGGCCGGCCGGCTAGCCCGGCTTCCGCCTGGGCCTCGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121537382..121537497 26863196 MeRIP-seq:(Medium) rs1555308927 Functional Loss SNV dbSNP153 33..33 33 - - - 92424 RMVar_ID_92424 Human_SNP_ID_518411136 m1A Human chr12 - 121537949 121537949 121537949 CCTCCGCAGCCGAAGGGGACGCCCGGGAGCCGAAGGGGACGCACGGGAGCCGCCGCCGCCGCCGC CCTCCGCAGCCGAAGGGGACGCCCGGGAGCCGGAGGGGACGCACGGGAGCCGCCGCCGCCGCCGC T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121537823..121538077 26863196 MeRIP-seq:(Medium) rs1160568873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_10764,RMVar_hsa_circ_309099,RMVar_hsa_circ_20833,RMVar_hsa_circ_15469,RMVar_hsa_circ_325352,RMVar_hsa_circ_14388,RMVar_hsa_circ_160928,RMVar_hsa_circ_302455,RMVar_hsa_circ_336377 92425 RMVar_ID_92425 Human_SNP_ID_518422241 m1A Human chr12 + 121580206 121580206 121580206 GCCGAGATCTACAAAGTTTTGCACCAACACTTAGGCAGATCCGTTTGCAAAGTCCTAGGAAACCA GCCGAGATCTACAAAGTTTTGCACCAACACTTTGGCAGATCCGTTTGCAAAGTCCTAGGAAACCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121580158..121580244 26863196 MeRIP-seq:(Medium) rs1000171238 Functional Loss SNV dbSNP153 33..33 33 - - - 92426 RMVar_ID_92426 Human_SNP_ID_518422363 m1A Human chr12 - 121580442 121580442 121580442 AGGCGCACTCGTGACCCAACAACAAAACAGCGATGCCACGGCGCTAACGGCGCCCGGTGCCTCCC AGGCGCACTCGTGACCCAACAACAAAACAGCGCTGCCACGGCGCTAACGGCGCCCGGTGCCTCCC T G KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121580394..121580560 26863196 MeRIP-seq:(Medium) rs1410684308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4206677 92427 RMVar_ID_92427 Human_SNP_ID_518461237 m1A Human chr12 + 121712848 121712848 121712848 GCGGGCGTGGGGCGCTGGGGGGCCGGTCGGGCAGCGCTGCGGGAGCAGCCGCCGGCACCGCCGCC GCGGGCGTGGGGCGCTGGGGGGCCGGTCGGGCCGCGCTGCGGGAGCAGCCGCCGGCACCGCCGCC A C TMEM120B Ensembl:ENSG00000188735 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121712801..121743660 26863196 MeRIP-seq:(Medium) rs928038281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229448,Human_RBP_ID_810611,Human_RBP_ID_876273,Human_RBP_ID_4246383,Human_RBP_ID_9352781,Human_RBP_ID_18417529 RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 92428 RMVar_ID_92428 Human_SNP_ID_518470574 m1A Human chr12 - 121747167 121747167 121747167 GATGCTGCCTCCCAGGTAGTCTTGTGACTTTCAGAAAGTCCTTAAACCTCTCTGCCTTATTTTCC GATGCTGCCTCCCAGGTAGTCTTGTGACTTTCGGAAAGTCCTTAAACCTCTCTGCCTTATTTTCC T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121747162..121747306 26863196 MeRIP-seq:(Medium) rs867565559 Functional Loss SNV dbSNP153 33..33 33 - - - 92429 RMVar_ID_92429 Human_SNP_ID_518470584 m1A Human chr12 - 121747205 121747205 121747205 CCGCAGTTCCCCATCTCAACTCTCGGGGTTGGAGGAGTGATGCTGCCTCCCAGGTAGTCTTGTGA CCGCAGTTCCCCATCTCAACTCTCGGGGTTGGGGGAGTGATGCTGCCTCCCAGGTAGTCTTGTGA T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121747200..121747332 26863196 MeRIP-seq:(Medium) rs1458115026 Functional Loss SNV dbSNP153 33..33 33 - - - 92430 RMVar_ID_92430 Human_SNP_ID_518470718 m1A Human chr12 + 121747573 121747571 121747573 AAGGCGGGAGGCTGGGGTAGAAGGCGGGAGGCACTGGGGTAGAAGGCGGGAGGCTGGGGTAGAAG AAGGCGGGAGGCTGGGGTAGAAGGCGGGAGG__CTGGGGTAGAAGGCGGGAGGCTGGGGTAGAAG GCA G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121747535..121747620 26863196 MeRIP-seq:(Medium) rs1566515572 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160942,RMVar_hsa_circ_273534,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939,RMVar_hsa_circ_362168,RMVar_hsa_circ_372610,RMVar_hsa_circ_289314,RMVar_hsa_circ_76846,RMVar_hsa_circ_95470,RMVar_hsa_circ_160944,RMVar_hsa_circ_160945,RMVar_hsa_circ_160943,RMVar_hsa_circ_160940,RMVar_hsa_circ_160941 92431 RMVar_ID_92431 Human_SNP_ID_518472564 m1A Human chr12 - 121753174 121753174 121753174 GACTGGTTCTTTAACTCAGCATCACATTTTCAAGGTTCATCCATGCTGCAGCCTGGCTCCGTACT GACTGGTTCTTTAACTCAGCATCACATTTTCACGGTTCATCCATGCTGCAGCCTGGCTCCGTACT T G lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121753125..121753328 26863196 MeRIP-seq:(Medium) rs940244141 Functional Loss SNV dbSNP153 33..33 33 - - - 92432 RMVar_ID_92432 Human_SNP_ID_518472594 m1A Human chr12 + 121753294 121753293 121753294 CTATAGAGACGGGGAGTAGGTGAGTGGTGGCCAGGGGCTGCGGGAGGCAGGAAGGAGGGCATGAC CTATAGAGACGGGGAGTAGGTGAGTGGTGGCC_GGGGCTGCGGGAGGCAGGAAGGAGGGCATGAC CA C TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121753094..121753337 26863196 MeRIP-seq:(Medium) rs1259837846 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6144471 RMVar_hsa_circ_6499,RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160942,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939,RMVar_hsa_circ_372610,RMVar_hsa_circ_289314,RMVar_hsa_circ_76846,RMVar_hsa_circ_95470,RMVar_hsa_circ_160944,RMVar_hsa_circ_160945,RMVar_hsa_circ_160943,RMVar_hsa_circ_371905,RMVar_hsa_circ_112218,RMVar_hsa_circ_160947,RMVar_hsa_circ_160948,RMVar_hsa_circ_97769,RMVar_hsa_circ_160949 92433 RMVar_ID_92433 Human_SNP_ID_518479263 m1A Human chr12 + 121776021 121776021 121776021 CCAGTCTTCCTGGGGATGGGGCCTGAAGCCTCAGGGAGCCCCTCTGTTCCCACTCCTGTCATTTG CCAGTCTTCCTGGGGATGGGGCCTGAAGCCTCGGGGAGCCCCTCTGTTCCCACTCCTGTCATTTG A G TMEM120B Ensembl:ENSG00000188735 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:121775970..121776164 32194978 MeRIP-seq:(Medium) rs1261704096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260136,Human_RBP_ID_4206765,Human_RBP_ID_8367763 Human_miRNA_ID_119476,Human_miRNA_ID_123283,Human_miRNA_ID_1003863,Human_miRNA_ID_1267097,Human_miRNA_ID_1973327,Human_miRNA_ID_1975503,Human_miRNA_ID_2390533,Human_miRNA_ID_2591775,Human_miRNA_ID_2613305,Human_miRNA_ID_3001606 RMVar_hsa_circ_91782,RMVar_hsa_circ_160939,RMVar_hsa_circ_95470,RMVar_hsa_circ_160945,RMVar_hsa_circ_105163,RMVar_hsa_circ_119183,RMVar_hsa_circ_160953,RMVar_hsa_circ_377348,RMVar_hsa_circ_160955,RMVar_hsa_circ_120307,RMVar_hsa_circ_160956,RMVar_hsa_circ_160957 92434 RMVar_ID_92434 Human_SNP_ID_518479802 m1A Human chr12 - 121777821 121777819 121777822 GCCTCATGATGGTCTACGGTAGAGGTCCAACAACTACAGCCTGTGGGCCACATCTGGCCACAGCC GCCTCATGATGGTCTACGGTAGAGGTCCAAC___TACAGCCTGTGGGCCACATCTGGCCACAGCC AGTT A RHOF Ensembl:ENSG00000139725 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:121777803..121777904 32194978 MeRIP-seq:(Medium) rs1212054446 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_413133,Human_RBP_ID_27419366 92435 RMVar_ID_92435 Human_SNP_ID_518479804 m1A Human chr12 - 121777821 121777821 121777821 GCCTCATGATGGTCTACGGTAGAGGTCCAACAACTACAGCCTGTGGGCCACATCTGGCCACAGCC GCCTCATGATGGTCTACGGTAGAGGTCCAACAGCTACAGCCTGTGGGCCACATCTGGCCACAGCC T C RHOF Ensembl:ENSG00000139725 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:121777803..121777904 32194978 MeRIP-seq:(Medium) rs1279553645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413133,Human_RBP_ID_27419366 92436 RMVar_ID_92436 Human_SNP_ID_518480170 m1A Human chr12 + 121779098 121779098 121779098 CAGTGGTGCCTATCTCGGGAGCCCAGGGAGGCAGGGACACAGGAGTGGCAGGCTTGGGGCGCCCG CAGTGGTGCCTATCTCGGGAGCCCAGGGAGGCGGGGACACAGGAGTGGCAGGCTTGGGGCGCCCG A G TMEM120B Ensembl:ENSG00000188735 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:121779049..121779199 32194978 MeRIP-seq:(Medium) rs1028717949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229456,Human_RBP_ID_413145,Human_RBP_ID_6144503 RMVar_hsa_circ_91782,RMVar_hsa_circ_160939,RMVar_hsa_circ_95470,RMVar_hsa_circ_160945,RMVar_hsa_circ_105163,RMVar_hsa_circ_119183,RMVar_hsa_circ_160953,RMVar_hsa_circ_377348,RMVar_hsa_circ_160955,RMVar_hsa_circ_120307,RMVar_hsa_circ_160956,RMVar_hsa_circ_160957 92437 RMVar_ID_92437 Human_SNP_ID_518480861 m1A Human chr12 - 121781099 121781099 121781099 CTGCTATGACGTCATGAATCCCACCAGCTACGACAACGTCCTCATCAAGGTGAGGCCGGCCTCCT CTGCTATGACGTCATGAATCCCACCAGCTACGCCAACGTCCTCATCAAGGTGAGGCCGGCCTCCT T G RHOF Ensembl:ENSG00000139725 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:121781076..121781100 26863196 MeRIP-seq:(Medium) rs755379087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35120 Human_Splice_Rec_1435670,Human_Splice_Rec_1435671,Human_Splice_Rec_1435676,Human_Splice_Rec_1435677,Human_Splice_Rec_1435684,Human_Splice_Rec_1435685,Human_Splice_Rec_1435692,Human_Splice_Rec_1435693,Human_Splice_Rec_1435702,Human_Splice_Rec_1435703,Human_Splice_Rec_1435710 Human_miRNA_ID_1962325 RMVar_hsa_circ_32048,RMVar_hsa_circ_286866,RMVar_hsa_circ_160958,RMVar_hsa_circ_378829,RMVar_hsa_circ_160959 92438 RMVar_ID_92438 Human_SNP_ID_518480887 m1A Human chr12 - 121781144 121781144 121781144 CCGGCTGCGGCCCCTGTCCTACCAGAACACCCACCTCGTGCTCATCTGCTATGACGTCATGAATC CCGGCTGCGGCCCCTGTCCTACCAGAACACCCGCCTCGTGCTCATCTGCTATGACGTCATGAATC T C RHOF Ensembl:ENSG00000139725 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr12:121780905..121781215;chr12:121780926..121781200 26863196 MeRIP-seq:(Medium) rs1438878634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35120,Human_RBP_ID_4247949 Human_Splice_Rec_1435670,Human_Splice_Rec_1435671,Human_Splice_Rec_1435676,Human_Splice_Rec_1435677,Human_Splice_Rec_1435684,Human_Splice_Rec_1435685,Human_Splice_Rec_1435692,Human_Splice_Rec_1435693,Human_Splice_Rec_1435702,Human_Splice_Rec_1435703,Human_Splice_Rec_1435710 RMVar_hsa_circ_32048,RMVar_hsa_circ_286866,RMVar_hsa_circ_160958,RMVar_hsa_circ_378829,RMVar_hsa_circ_160959 92439 RMVar_ID_92439 Human_SNP_ID_518481681 m1A Human chr12 - 121783908 121783908 121783908 AGGGGAGATGTTTGGATTTTATGCAAAGGGCAATAGGGGCCAGGCACGGTGGCTCATGCCTATAA AGGGGAGATGTTTGGATTTTATGCAAAGGGCAGTAGGGGCCAGGCACGGTGGCTCATGCCTATAA T C RHOF Ensembl:ENSG00000139725 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121783906..121784089 26863196 MeRIP-seq:(Medium) rs564669552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378829 92440 RMVar_ID_92440 Human_SNP_ID_518484238 m1A Human chr12 + 121793164 121793163 121793165 CGGCGCGCAGGCGCACTCACCGGCCGTGTCGTAGAGGTTCAGGGTCACCTCCTTGCTGCCAACGG CGGCGCGCAGGCGCACTCACCGGCCGTGTCGT__AGGTTCAGGGTCACCTCCTTGCTGCCAACGG TAG T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121793151..121793250 26863196 MeRIP-seq:(Medium) rs760785782 Functional Loss DEL dbSNP153 33..34 33 - - - 92441 RMVar_ID_92441 Human_SNP_ID_518487942 m1A Human chr12 - 121803459 121803459 121803459 CCTCCCCGGAGCTGAGCTGGGGAAGGGAGACCAGGGTTCACCACGTTAGCATTCGCATTCCTGGG CCTCCCCGGAGCTGAGCTGGGGAAGGGAGACCCGGGTTCACCACGTTAGCATTCGCATTCCTGGG T G LINC01089 Ensembl:ENSG00000212694 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:121803409..121803510 32194978 MeRIP-seq:(Medium) rs1206448850 Functional Loss SNV dbSNP153 33..33 33 - - - 92442 RMVar_ID_92442 Human_SNP_ID_518488107 m1A Human chr12 + 121803892 121803892 121803892 GGGGCCGCTGGGGCCCGGGGCTTTGGCGGCGCAGCTGCCGCCGCCGGGAGAGTGCCTGGGGAAGC GGGGCCGCTGGGGCCCGGGGCTTTGGCGGCGCGGCTGCCGCCGCCGGGAGAGTGCCTGGGGAAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121803805..121803906 26863196 MeRIP-seq:(Medium) rs1452806061 Functional Loss SNV dbSNP153 33..33 33 - - - 92443 RMVar_ID_92443 Human_SNP_ID_518488187 m1A Human chr12 + 121804074 121804074 121804074 CCTCCGCCGCCAGCCGCCTCCCGGGCAGCAGCAGCAGCAGCGGCGGCGGCAGCGGCAGCAGCTCC CCTCCGCCGCCAGCCGCCTCCCGGGCAGCAGCGGCAGCAGCGGCGGCGGCAGCGGCAGCAGCTCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:121804026..121804188 26863196 MeRIP-seq:(Medium) rs1327148541 Functional Loss SNV dbSNP153 33..33 33 - - - 92444 RMVar_ID_92444 Human_SNP_ID_518488201 m1A Human chr12 + 121804092 121804086 121804092 TCCCGGGCAGCAGCAGCAGCAGCGGCGGCGGCAGCGGCAGCAGCTCCGGGCCCGGCAGCCGCGGC TCCCGGGCAGCAGCAGCAGCAGCGGCG______GCGGCAGCAGCTCCGGGCCCGGCAGCCGCGGC GGCGGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121804042..121804204 26863196 MeRIP-seq:(Medium) rs924808280 Functional Loss DEL dbSNP153 28..33 33 - - - 92445 RMVar_ID_92445 Human_SNP_ID_518488204 m1A Human chr12 + 121804092 121804092 121804092 TCCCGGGCAGCAGCAGCAGCAGCGGCGGCGGCAGCGGCAGCAGCTCCGGGCCCGGCAGCCGCGGC TCCCGGGCAGCAGCAGCAGCAGCGGCGGCGGCGGCGGCAGCAGCTCCGGGCCCGGCAGCCGCGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121804042..121804204 26863196 MeRIP-seq:(Medium) rs1232632011 Functional Loss SNV dbSNP153 33..33 33 - - - 92446 RMVar_ID_92446 Human_SNP_ID_518488211 m1A Human chr12 - 121804104 121804104 121804104 GGGGGCGCCGCCGCCGCGGCTGCCGGGCCCGGAGCTGCTGCCGCTGCCGCCGCCGCTGCTGCTGC GGGGGCGCCGCCGCCGCGGCTGCCGGGCCCGGCGCTGCTGCCGCTGCCGCCGCCGCTGCTGCTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121803931..121804285 26863196 MeRIP-seq:(Medium) rs932608877 Functional Loss SNV dbSNP153 33..33 33 - - - 92447 RMVar_ID_92447 Human_SNP_ID_518488264 m1A Human chr12 + 121804213 121804213 121804213 GGGGACACCATGTACTGGCTGGCGGCGCAGGGAGGCCGGCGCCCGGCGGGGATGTAAGCGCGGCT GGGGACACCATGTACTGGCTGGCGGCGCAGGGGGGCCGGCGCCCGGCGGGGATGTAAGCGCGGCT A G SETD1B Ensembl:ENSG00000139718 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121803922..121804278 26863196 MeRIP-seq:(Medium) rs1030262127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230031,Human_RBP_ID_754869,Human_RBP_ID_3418514,Human_RBP_ID_4247952,Human_RBP_ID_5314693,Human_RBP_ID_8230079,Human_RBP_ID_9323291 Human_Splice_Rec_1435793,Human_Splice_Rec_1435823 92448 RMVar_ID_92448 Human_SNP_ID_518488510 m1A Human chr12 + 121804772 121804770 121804773 GGAGAACAGTCACCCCCCCCACCACCACCACCAGCAGCCCCCGCCGCAGCCCGGCCCTTCGGGCG GGAGAACAGTCACCCCCCCCACCACCACCAC___CAGCCCCCGCCGCAGCCCGGCCCTTCGGGCG CCAG C SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121804681..121804850 26863196 MeRIP-seq:(Medium) rs879887994 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3943693,Human_RBP_ID_27419401 Human_Splice_Rec_1435794,Human_Splice_Rec_1435824 RMVar_hsa_circ_339239 92449 RMVar_ID_92449 Human_SNP_ID_518488512 m1A Human chr12 + 121804772 121804772 121804772 GGAGAACAGTCACCCCCCCCACCACCACCACCAGCAGCCCCCGCCGCAGCCCGGCCCTTCGGGCG GGAGAACAGTCACCCCCCCCACCACCACCACCGGCAGCCCCCGCCGCAGCCCGGCCCTTCGGGCG A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121804681..121804850 26863196 MeRIP-seq:(Medium) rs1316945004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3943693,Human_RBP_ID_27419401 Human_Splice_Rec_1435794,Human_Splice_Rec_1435824 RMVar_hsa_circ_339239 92450 RMVar_ID_92450 Human_SNP_ID_518490101 m1A Human chr12 + 121809864 121809864 121809864 CCTCATACCTCTTCAGCCAGGACCCTGCAGTGACCTTCAAGGCCCGGCGCCACGAGAGCAAGTTC CCTCATACCTCTTCAGCCAGGACCCTGCAGTGGCCTTCAAGGCCCGGCGCCACGAGAGCAAGTTC A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121809814..121809967 26863196 MeRIP-seq:(Medium) rs1468185202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6144542 92451 RMVar_ID_92451 Human_SNP_ID_518490301 m1A Human chr12 + 121810278 121810278 121810278 CCCCACCCCTGCCACCTGCTGAGCCTCTGGCCAAGGAGAAGCCAGGCACGCCACCCGGCCCGCCG CCCCACCCCTGCCACCTGCTGAGCCTCTGGCCGAGGAGAAGCCAGGCACGCCACCCGGCCCGCCG A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121810227..121810368 26863196 MeRIP-seq:(Medium) rs558470422 Functional Loss SNV dbSNP153 33..33 33 - - - 92452 RMVar_ID_92452 Human_SNP_ID_518490412 m1A Human chr12 + 121810515 121810515 121810515 AGCTGCTCTTCCTGAGGGAGCCGGACTCGGACACCGAGCTGCAGATGGAGGGCAGCCCCATCTCC AGCTGCTCTTCCTGAGGGAGCCGGACTCGGACGCCGAGCTGCAGATGGAGGGCAGCCCCATCTCC A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121810466..121810619 26863196 MeRIP-seq:(Medium) rs1219688296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17811432,Human_RBP_ID_27419417,Human_RBP_ID_27557721 92453 RMVar_ID_92453 Human_SNP_ID_518491612 m1A Human chr12 + 121814493 121814493 121814493 CGCCGGGCCTGTTCCCTGTGATGCAGGTGGACATGAGCCACGTGCTGGGTGGCCAGTGGGGCGGC CGCCGGGCCTGTTCCCTGTGATGCAGGTGGACGTGAGCCACGTGCTGGGTGGCCAGTGGGGCGGC A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121814442..121814531 26863196 MeRIP-seq:(Medium) rs1417003991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413169,Human_RBP_ID_3942299,Human_RBP_ID_5127230,Human_RBP_ID_8787006,Human_RBP_ID_9279335,Human_RBP_ID_17075186,Human_RBP_ID_17811435,Human_RBP_ID_18935763,Human_RBP_ID_22039626 92454 RMVar_ID_92454 Human_SNP_ID_518492559 m1A Human chr12 - 121817446 121817446 121817446 AGCTCCAGAGGCCGCGCCGGCCGCCGCCGCACACCCACGCCCTTGGGGTCCCGCTTGGCGAGCTC AGCTCCAGAGGCCGCGCCGGCCGCCGCCGCACTCCCACGCCCTTGGGGTCCCGCTTGGCGAGCTC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121817330..121817900 26863196 MeRIP-seq:(Medium) rs1021810527 Functional Loss SNV dbSNP153 33..33 33 - - - 92455 RMVar_ID_92455 Human_SNP_ID_518492577 m1A Human chr12 + 121817475 121817475 121817475 GGGTGTGCGGCGGCGGCCGGCGCGGCCTCTGGAGCTGGACAGTGGTGGGGAGGAGGACGAGAAGG GGGTGTGCGGCGGCGGCCGGCGCGGCCTCTGGGGCTGGACAGTGGTGGGGAGGAGGACGAGAAGG A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121817425..121817725 26863196 MeRIP-seq:(Medium) rs1035748037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230038,Human_RBP_ID_755733,Human_RBP_ID_5521830,Human_RBP_ID_5554736 RMVar_hsa_circ_12018 92456 RMVar_ID_92456 Human_SNP_ID_518492668 m1A Human chr12 - 121817672 121817670 121817673 CTTATCTGATGTGGATGAGGTTGAGGAGGAGGAGAGCTGGCTCCTGGGGACTTCCTCCTCCTCCT CTTATCTGATGTGGATGAGGTTGAGGAGGAG___AGCTGGCTCCTGGGGACTTCCTCCTCCTCCT TCTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121817621..121817705 26863196 MeRIP-seq:(Medium) rs1220241283 Functional Loss DEL dbSNP153 32..34 33 - - - 92457 RMVar_ID_92457 Human_SNP_ID_518492669 m1A Human chr12 - 121817672 121817672 121817672 CTTATCTGATGTGGATGAGGTTGAGGAGGAGGAGAGCTGGCTCCTGGGGACTTCCTCCTCCTCCT CTTATCTGATGTGGATGAGGTTGAGGAGGAGGCGAGCTGGCTCCTGGGGACTTCCTCCTCCTCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121817621..121817705 26863196 MeRIP-seq:(Medium) rs1423785992 Functional Loss SNV dbSNP153 33..33 33 - - - 92458 RMVar_ID_92458 Human_SNP_ID_518493326 m1A Human chr12 - 121819572 121819572 121819572 CAGGGCCTGCAGAAGCCATGCTTTCCTCGGCCACCATCTCCTCCTCCTCCTCTTCTTCCTCCTCT CAGGGCCTGCAGAAGCCATGCTTTCCTCGGCCTCCATCTCCTCCTCCTCCTCTTCTTCCTCCTCT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:121819526..121819725 26863196 MeRIP-seq:(Medium) rs188280904 Functional Loss SNV dbSNP153 33..33 33 - - - 92459 RMVar_ID_92459 Human_SNP_ID_518493342 m1A Human chr12 + 121819620 121819620 121819620 GGCTTCTGCAGGCCCTGAGGACTTTGAGCAGGACGGGGAGGAAGCGGCTCTGGCCCCGGGGGCAC GGCTTCTGCAGGCCCTGAGGACTTTGAGCAGGGCGGGGAGGAAGCGGCTCTGGCCCCGGGGGCAC A G SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:121819570..121819712 26863196 MeRIP-seq:(Medium) rs1414382014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521834,Human_RBP_ID_6144555,Human_RBP_ID_22039630,Human_RBP_ID_27419425 RMVar_hsa_circ_323997 92460 RMVar_ID_92460 Human_SNP_ID_518494234 m1A Human chr12 + 121822544 121822544 121822544 GGAGCCCCCTATGATGCTCCCCTTGCCGCTGCAACCACCATTGCCGCCCCCACGACCACCCCGGC GGAGCCCCCTATGATGCTCCCCTTGCCGCTGCCACCACCATTGCCGCCCCCACGACCACCCCGGC A C SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121822479..121822640 26863196 MeRIP-seq:(Medium) rs1362955291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875309,Human_RBP_ID_8367802 Human_Splice_Rec_1435814,Human_Splice_Rec_1435844,Human_Splice_Rec_1435872,Human_Splice_Rec_1435900 92461 RMVar_ID_92461 Human_SNP_ID_518494258 m1A Human chr12 + 121822587 121822587 121822587 CCGCCCCCACGACCACCCCGGCCACCCAGCCCACCGCCGGAGCCTGAGACCACAGATGCCTCACA CCGCCCCCACGACCACCCCGGCCACCCAGCCCCCCGCCGGAGCCTGAGACCACAGATGCCTCACA A C SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121822543..121822693 26863196 MeRIP-seq:(Medium) rs775255325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1435814,Human_Splice_Rec_1435844,Human_Splice_Rec_1435872,Human_Splice_Rec_1435900 92462 RMVar_ID_92462 Human_SNP_ID_518494406 m1A Human chr12 - 121822910 121822910 121822910 GTCGGCCAGTGGGGAGTGGGCAGACGGGCAGGAGCAAGGGCCCGCTGGGCTCGGAGAAGGTGGGT GTCGGCCAGTGGGGAGTGGGCAGACGGGCAGGCGCAAGGGCCCGCTGGGCTCGGAGAAGGTGGGT T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:121822860..121823119 26863196 MeRIP-seq:(Medium) rs757578120 Functional Loss SNV dbSNP153 33..33 33 - - - 92463 RMVar_ID_92463 Human_SNP_ID_518494462 m1A Human chr12 - 121823012 121823012 121823012 CGGCGGGCAATGCCAAGGGCAAGGGCAGGGGAAGGGGCAGAGGGAGGGGCAGGCCCGTCTCCAGG CGGCGGGCAATGCCAAGGGCAAGGGCAGGGGAGGGGGCAGAGGGAGGGGCAGGCCCGTCTCCAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:121822876..121823282 26863196 MeRIP-seq:(Medium) rs1379233693 Functional Loss SNV dbSNP153 33..33 33 - - - 92464 RMVar_ID_92464 Human_SNP_ID_518500497 m1A Human chr12 - 121843305 121843305 121843305 CATGCCCTGAGCGTCTGAGGAACAGAAAGAATAGGCTAGAGTGGATGGGAGGCTGTTTTTGAGCG CATGCCCTGAGCGTCTGAGGAACAGAAAGAATGGGCTAGAGTGGATGGGAGGCTGTTTTTGAGCG T C HPD Ensembl:ENSG00000158104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121843301..121843507 26863196 MeRIP-seq:(Medium) rs973294738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53858,RMVar_hsa_circ_87811,RMVar_hsa_circ_160967 92465 RMVar_ID_92465 Human_SNP_ID_518501554 m1A Human chr12 + 121846950 121846948 121846951 TATAGTCCACATATTCCTGGGGGAGGGAAACAAGGAGACCACTGTCATTTGCCCCATCACCCACA TATAGTCCACATATTCCTGGGGGAGGGAAAC___GAGACCACTGTCATTTGCCCCATCACCCACA CAAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121846948..121847042 26863196 MeRIP-seq:(Medium) rs1231759368 Functional Loss DEL dbSNP153 32..34 33 - - - 92466 RMVar_ID_92466 Human_SNP_ID_518504596 m1A Human chr12 - 121857306 121857306 121857306 AACAAGGGAAGGTGAGTCACCACCCCCAGGACAGCCCCCAACCCCTGCCTGGCCAACATGGTGAA AACAAGGGAAGGTGAGTCACCACCCCCAGGACGGCCCCCAACCCCTGCCTGGCCAACATGGTGAA T C HPD Ensembl:ENSG00000158104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121857301..121857325 26863196 MeRIP-seq:(Medium) rs542256602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19057030 RMVar_hsa_circ_87811,RMVar_hsa_circ_160967,RMVar_hsa_circ_74191,RMVar_hsa_circ_361490 92467 RMVar_ID_92467 Human_SNP_ID_518504707 m1A Human chr12 - 121857643 121857642 121857643 TGTGATTGGCCCTTGGGAGGGAGGATCAGGCCAGGGGTGGGCCAGATACTCTGAATCCTAATTAC TGTGATTGGCCCTTGGGAGGGAGGATCAGGCC_GGGGTGGGCCAGATACTCTGAATCCTAATTAC CT C HPD Ensembl:ENSG00000158104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121857642..121857766 26863196 MeRIP-seq:(Medium) rs1426693207 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5348857 RMVar_hsa_circ_74191,RMVar_hsa_circ_361490 92468 RMVar_ID_92468 Human_SNP_ID_518512604 m1A Human chr12 + 121888911 121888911 121888911 AGAGCGGAGGCTCCTCGCAGGCCGGCGTCGTGACTGTCAGCGACGTCCAGGAGCTGATGCGGCGC AGAGCGGAGGCTCCTCGCAGGCCGGCGTCGTGGCTGTCAGCGACGTCCAGGAGCTGATGCGGCGC A G PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:121888826..121888975 26863410 MeRIP-seq:(Medium) rs1349486934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413189,Human_RBP_ID_753171,Human_RBP_ID_4247087 Human_Splice_Rec_1435983,Human_Splice_Rec_1435995,Human_Splice_Rec_1436003,Human_Splice_Rec_1436013,Human_Splice_Rec_1436017,Human_Splice_Rec_1436023,Human_Splice_Rec_1436033,Human_Splice_Rec_1436063 Human_miRNA_ID_2509408 RMVar_hsa_circ_160970,RMVar_hsa_circ_92659 92469 RMVar_ID_92469 Human_SNP_ID_518515501 m1A Human chr12 + 121899777 121899777 121899777 AGGCCATGAGCCGCAAACTGGGTCAGAGTGAGAGCCAGGGCCCTCCACGGGCCTTCGCCAAAGTG AGGCCATGAGCCGCAAACTGGGTCAGAGTGAGTGCCAGGGCCCTCCACGGGCCTTCGCCAAAGTG A T PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:121899726..121899825 32194978 MeRIP-seq:(Medium) rs753485859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876031,Human_RBP_ID_4207095,Human_RBP_ID_8367818,Human_RBP_ID_23543272 Human_Splice_Rec_1435987,Human_Splice_Rec_1436007,Human_Splice_Rec_1436027,Human_Splice_Rec_1436051 RMVar_hsa_circ_160970,RMVar_hsa_circ_92659,RMVar_hsa_circ_160971,RMVar_hsa_circ_274514,RMVar_hsa_circ_282670 92470 RMVar_ID_92470 Human_SNP_ID_518520007 m1A Human chr12 + 121916291 121916291 121916291 CCATTCCTTTTCTTCTTTCTTCCAGCTGCAACATTATTCCTCTGCAAAGATGATTGTCCCTGGGG CCATTCCTTTTCTTCTTTCTTCCAGCTGCAACGTTATTCCTCTGCAAAGATGATTGTCCCTGGGG A G PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:121916276..121916426 32194978 MeRIP-seq:(Medium) rs766842397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18256405,Human_RBP_ID_26902499 Human_Splice_Rec_1435994,Human_Splice_Rec_1436002,Human_Splice_Rec_1436012,Human_Splice_Rec_1436022,Human_Splice_Rec_1436032,Human_Splice_Rec_1436042,Human_Splice_Rec_1436050,Human_Splice_Rec_1436056,Human_Splice_Rec_1436060,Human_Splice_Rec_1436062 92471 RMVar_ID_92471 Human_SNP_ID_518546819 m1A Human chr12 + 122022088 122022088 122022088 GGCGCGCTCCCCAGCCTCCGTCTCCCCGCCGGAACCATGTCGGGCAGGTCGGTTCGAGCCGAGAC GGCGCGCTCCCCAGCCTCCGTCTCCCCGCCGGGACCATGTCGGGCAGGTCGGTTCGAGCCGAGAC A G BCL7A Ensembl:ENSG00000110987 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEPG2 cell line,total RNA Untreated chr12:122022000..122022087;chr12:122021955..122022175 26863410,26863196 MeRIP-seq:(Medium) rs1242594485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5416745,Human_RBP_ID_5437370,Human_RBP_ID_5461501,Human_RBP_ID_5491064,Human_RBP_ID_5645025,Human_RBP_ID_17683608,Human_RBP_ID_17811489,Human_RBP_ID_22793331,Human_RBP_ID_23543356 Human_Splice_Rec_1436185,Human_Splice_Rec_1436195,Human_Splice_Rec_1436205 92472 RMVar_ID_92472 Human_SNP_ID_518546851 m1A Human chr12 + 122022149 122022149 122022149 AGACGAGGAGCCGGGCCAAAGATGATATCAAGAGGGTCATGGCGGCGATCGAGAAAGTGCGCAAA AGACGAGGAGCCGGGCCAAAGATGATATCAAGTGGGTCATGGCGGCGATCGAGAAAGTGCGCAAA A T BCL7A Ensembl:ENSG00000110987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122021909..122022229 26863196 MeRIP-seq:(Medium) rs1215968468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4207172,Human_RBP_ID_23543362 Human_Splice_Rec_1436185,Human_Splice_Rec_1436195,Human_Splice_Rec_1436205 92473 RMVar_ID_92473 Human_SNP_ID_518546864 m1A Human chr12 - 122022182 122022182 122022182 GAGGCGGCTGGCGGCGGGCGCCTCCGCTTACCATTTGCGCACTTTCTCGATCGCCGCCATGACCC GAGGCGGCTGGCGGCGGGCGCCTCCGCTTACCTTTTGCGCACTTTCTCGATCGCCGCCATGACCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122022156..122030772 32194978 MeRIP-seq:(Medium) rs756357727 Functional Loss SNV dbSNP153 33..33 33 - - - 92474 RMVar_ID_92474 Human_SNP_ID_518546877 m1A Human chr12 + 122022192 122022192 122022192 GGCGATCGAGAAAGTGCGCAAATGGTAAGCGGAGGCGCCCGCCGCCAGCCGCCTCCCCGGCCGCC GGCGATCGAGAAAGTGCGCAAATGGTAAGCGGCGGCGCCCGCCGCCAGCCGCCTCCCCGGCCGCC A C BCL7A Ensembl:ENSG00000110987 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:122022176..122022200 26863196 MeRIP-seq:(Medium) rs1324815665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059544 92475 RMVar_ID_92475 Human_SNP_ID_518547283 m1A Human chr12 + 122023365 122023365 122023365 TCGACCCTTTATTTCGAGCCTGGAAGCTGGGCAGGCCCTGTGGCAGGGGATGTTTACGTTTGGGG TCGACCCTTTATTTCGAGCCTGGAAGCTGGGCTGGCCCTGTGGCAGGGGATGTTTACGTTTGGGG A T BCL7A Ensembl:ENSG00000110987 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:122023269..122023453 26863196 MeRIP-seq:(Medium) rs181225670 Functional Loss SNV dbSNP153 33..33 33 - - - 92476 RMVar_ID_92476 Human_SNP_ID_518557775 m1A Human chr12 + 122060403 122060403 122060403 GGCCACAAACAAGGCGTCGAGGAATTGGAAAGATTTGCACACCCTCCAGAAAGGAGAGACGCAAT GGCCACAAACAAGGCGTCGAGGAATTGGAAAGGTTTGCACACCCTCCAGAAAGGAGAGACGCAAT A G BCL7A Ensembl:ENSG00000110987 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122060352..122060453 32194978 MeRIP-seq:(Medium) rs1385309858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1466377,Human_RBP_ID_1789165,Human_RBP_ID_5256316,Human_RBP_ID_8367896,Human_RBP_ID_11852677 92477 RMVar_ID_92477 Human_SNP_ID_518562397 m1A Human chr12 - 122078852 122078852 122078852 GCGGGGAGCACATGAAGACGTCGGCGGCCATGAGAAGGGCTCGGCCGGGGGCATCCCCCGGAGCC GCGGGGAGCACATGAAGACGTCGGCGGCCATGGGAAGGGCTCGGCCGGGGGCATCCCCCGGAGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:122078751..122079125 26863410 MeRIP-seq:(Medium) rs1008641599 Functional Loss SNV dbSNP153 33..33 33 - - - 92478 RMVar_ID_92478 Human_SNP_ID_518562399 m1A Human chr12 - 122078855 122078855 122078855 GGCGCGGGGAGCACATGAAGACGTCGGCGGCCATGAGAAGGGCTCGGCCGGGGGCATCCCCCGGA GGCGCGGGGAGCACATGAAGACGTCGGCGGCCGTGAGAAGGGCTCGGCCGGGGGCATCCCCCGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122078808..122079127 26863196 MeRIP-seq:(Medium) rs1471097298 Functional Loss SNV dbSNP153 33..33 33 - - - 92479 RMVar_ID_92479 Human_SNP_ID_518566225 m1A Human chr12 - 122093820 122093817 122093821 CAAACACACACCCCACACACACTGACACACACACCAACACACGACACACACCGACACACACAGAC CAAACACACACCCCACACACACTGACACACA____AACACACGACACACACCGACACACACAGAC TGGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:122093551..122094740 26863196 MeRIP-seq:(Medium) rs1317279149 Functional Loss DEL dbSNP153 32..35 33 - - - 92480 RMVar_ID_92480 Human_SNP_ID_518577115 m1A Human chr12 + 122133636 122133636 122133636 TACCATTAGTTCCTCCTCCTGCCACTGCCCTGAACCCCCCGGCTCCACCCACCTTCCATCAGCCA TACCATTAGTTCCTCCTCCTGCCACTGCCCTGGACCCCCCGGCTCCACCCACCTTCCATCAGCCA A G MLXIP Ensembl:ENSG00000175727 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122133326..122133975 26863196 MeRIP-seq:(Medium) rs1473066421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754277,Human_RBP_ID_5126965,Human_RBP_ID_11853754,Human_RBP_ID_17075189,Human_RBP_ID_17811561,Human_RBP_ID_18934830,Human_RBP_ID_27419536 Human_miRNA_ID_828965,Human_miRNA_ID_2353793 RMVar_hsa_circ_161008,RMVar_hsa_circ_76768 92481 RMVar_ID_92481 Human_SNP_ID_518577152 m1A Human chr12 - 122133740 122133740 122133740 CCCTGACTCTGGCTAAAGGTGGTGGCGGGGGCATCGTGGGTGAGGGTGGCAGAGGCCGTGTGGGT CCCTGACTCTGGCTAAAGGTGGTGGCGGGGGCGTCGTGGGTGAGGGTGGCAGAGGCCGTGTGGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:122133366..122133915;chr12:122133332..122133914 26863196 MeRIP-seq:(Medium) rs780039151 Functional Loss SNV dbSNP153 33..33 33 - - - 92482 RMVar_ID_92482 Human_SNP_ID_518577153 m1A Human chr12 - 122133740 122133740 122133740 CCCTGACTCTGGCTAAAGGTGGTGGCGGGGGCATCGTGGGTGAGGGTGGCAGAGGCCGTGTGGGT CCCTGACTCTGGCTAAAGGTGGTGGCGGGGGCCTCGTGGGTGAGGGTGGCAGAGGCCGTGTGGGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:122133366..122133915;chr12:122133332..122133914 26863196 MeRIP-seq:(Medium) rs780039151 Functional Loss SNV dbSNP153 33..33 33 - - - 92483 RMVar_ID_92483 Human_SNP_ID_518577830 m1A Human chr12 - 122135653 122135653 122135653 CCGCCGAGTGAACACTCACTGGGCCCTGTGACAGTGACCTGGGGGCTGCCCCCATGCAGCGGGAC CCGCCGAGTGAACACTCACTGGGCCCTGTGACTGTGACCTGGGGGCTGCCCCCATGCAGCGGGAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:122135476..122135700;chr12:122135526..122135725;chr12:122135508..122135725 26863196 MeRIP-seq:(Medium) rs1324306420 Functional Loss SNV dbSNP153 33..33 33 - - - 92484 RMVar_ID_92484 Human_SNP_ID_518577831 m1A Human chr12 - 122135653 122135653 122135653 CCGCCGAGTGAACACTCACTGGGCCCTGTGACAGTGACCTGGGGGCTGCCCCCATGCAGCGGGAC CCGCCGAGTGAACACTCACTGGGCCCTGTGACGGTGACCTGGGGGCTGCCCCCATGCAGCGGGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:122135476..122135700;chr12:122135526..122135725;chr12:122135508..122135725 26863196 MeRIP-seq:(Medium) rs1324306420 Functional Loss SNV dbSNP153 33..33 33 - - - 92485 RMVar_ID_92485 Human_SNP_ID_518579724 m1A Human chr12 - 122141814 122141814 122141814 TGGCATCTCATGCGGCCACATGCCAGCTAAGCAGCTAGGACTCTCCCAATCTCTTGCCAATCCTG TGGCATCTCATGCGGCCACATGCCAGCTAAGCCGCTAGGACTCTCCCAATCTCTTGCCAATCCTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122141764..122142363 32194978 MeRIP-seq:(Medium) rs893750635 Functional Loss SNV dbSNP153 33..33 33 - - - 92486 RMVar_ID_92486 Human_SNP_ID_518580770 m1A Human chr12 - 122145599 122145599 122145599 CCAGCTAGGGCCTTGGAGGAAGGGGCCTCGCCAGTTCTCAGCTGCAGCTCCCCTCTATGAGAGAG CCAGCTAGGGCCTTGGAGGAAGGGGCCTCGCCCGTTCTCAGCTGCAGCTCCCCTCTATGAGAGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122145552..122145653 32194978 MeRIP-seq:(Medium) rs902509032 Functional Loss SNV dbSNP153 33..33 33 - - - 92487 RMVar_ID_92487 Human_SNP_ID_518599232 m1A Human chr12 - 122208505 122208505 122208505 GCTGGTGAAACTGCAGGTGGAAGAGGTGCACCAGCTCTCCCGGAAAGCAGAAACCAAGCTGGCAG GCTGGTGAAACTGCAGGTGGAAGAGGTGCACCGGCTCTCCCGGAAAGCAGAAACCAAGCTGGCAG T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding CDS,3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:122208456..122208575 32194978 MeRIP-seq:(Medium) rs1448019291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755139 Human_Splice_Rec_1436410,Human_Splice_Rec_1436422,Human_Splice_Rec_1436444,Human_Splice_Rec_1436456,Human_Splice_Rec_1436464,Human_Splice_Rec_1436476,Human_Splice_Rec_1436484,Human_Splice_Rec_1436494,Human_Splice_Rec_1436502,Human_Splice_Rec_1436514,Human_Splice_Rec_1436518,Human_Splice_Rec_1436528,Human_Splice_Rec_1436536,Human_Splice_Rec_1436544,Human_Splice_Rec_1436552,Human_Splice_Rec_1436558,Human_Splice_Rec_1436568,Human_Splice_Rec_1436608 92488 RMVar_ID_92488 Human_SNP_ID_518599233 m1A Human chr12 - 122208505 122208505 122208505 GCTGGTGAAACTGCAGGTGGAAGAGGTGCACCAGCTCTCCCGGAAAGCAGAAACCAAGCTGGCAG GCTGGTGAAACTGCAGGTGGAAGAGGTGCACCCGCTCTCCCGGAAAGCAGAAACCAAGCTGGCAG T G DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding CDS,3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:122208456..122208575 32194978 MeRIP-seq:(Medium) rs1448019291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755139 Human_Splice_Rec_1436410,Human_Splice_Rec_1436422,Human_Splice_Rec_1436444,Human_Splice_Rec_1436456,Human_Splice_Rec_1436464,Human_Splice_Rec_1436476,Human_Splice_Rec_1436484,Human_Splice_Rec_1436494,Human_Splice_Rec_1436502,Human_Splice_Rec_1436514,Human_Splice_Rec_1436518,Human_Splice_Rec_1436528,Human_Splice_Rec_1436536,Human_Splice_Rec_1436544,Human_Splice_Rec_1436552,Human_Splice_Rec_1436558,Human_Splice_Rec_1436568,Human_Splice_Rec_1436608 92489 RMVar_ID_92489 Human_SNP_ID_518604863 m1A Human chr12 + 122225996 122225996 122225996 CCTGAAGAATGAAGTTACGCTGCGCGACAGCCAACTCTTCAGAGCCGCCATTGTGCAGCGCGCGG CCTGAAGAATGAAGTTACGCTGCGCGACAGCCTACTCTTCAGAGCCGCCATTGTGCAGCGCGCGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122225857..122226000 26863196 MeRIP-seq:(Medium) rs139511903 Functional Loss SNV dbSNP153 33..33 33 - - - 92490 RMVar_ID_92490 Human_SNP_ID_518606526 m1A Human chr12 - 122231900 122231900 122231900 GGCATGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGCCATGGTGTTTCACCATGTTGG GGCATGCACCACCACACCCGGCTAATTTTTGTTTTTTTAGTAGCCATGGTGTTTCACCATGTTGG T A VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12816400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11854737,Human_RBP_ID_24406565 RMVar_hsa_circ_266437 92491 RMVar_ID_92491 Human_SNP_ID_518606527 m1A Human chr12 - 122231900 122231900 122231900 GGCATGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGCCATGGTGTTTCACCATGTTGG GGCATGCACCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGCCATGGTGTTTCACCATGTTGG T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12816400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11854737,Human_RBP_ID_24406565 RMVar_hsa_circ_266437 92492 RMVar_ID_92492 Human_SNP_ID_518615963 m1A Human chr12 - 122266414 122266414 122266414 CTCGGTTGGCGTTGTGGGGCAGGGGGTGGTGGAGCAAGATGGCGGCTCATCTGTCCTACGGCCGA CTCGGTTGGCGTTGTGGGGCAGGGGGTGGTGGGGCAAGATGGCGGCTCATCTGTCCTACGGCCGA T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122264165..122266428 26863196 MeRIP-seq:(Medium) rs569562977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246389 92493 RMVar_ID_92493 Human_SNP_ID_518631413 m1A Human chr12 - 122328099 122328099 122328099 GTCAGGAGCTGAAAGCCAGGTATGAGAGAGCCACTTCTGAGACAAAAACCAAGCATGAAGAAATC GTCAGGAGCTGAAAGCCAGGTATGAGAGAGCCTCTTCTGAGACAAAAACCAAGCATGAAGAAATC T A CLIP1 Ensembl:ENSG00000130779 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122328051..122328325 26863196 MeRIP-seq:(Medium) rs1555264879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11855396,Human_RBP_ID_24543176,Human_RBP_ID_26322207 Human_Splice_Rec_1436774,Human_Splice_Rec_1436814,Human_Splice_Rec_1436860,Human_Splice_Rec_1436908,Human_Splice_Rec_1436958,Human_Splice_Rec_1437004,Human_Splice_Rec_1437044,Human_Splice_Rec_1437106 Human_miRNA_ID_181234 RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_269181,RMVar_hsa_circ_268219,RMVar_hsa_circ_161041,RMVar_hsa_circ_360514,RMVar_hsa_circ_360846,RMVar_hsa_circ_268999,RMVar_hsa_circ_31445,RMVar_hsa_circ_161045,RMVar_hsa_circ_331709,RMVar_hsa_circ_161042,RMVar_hsa_circ_359262,RMVar_hsa_circ_367744,RMVar_hsa_circ_372327,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_120675,RMVar_hsa_circ_161046,RMVar_hsa_circ_161047,RMVar_hsa_circ_57681,RMVar_hsa_circ_357637,RMVar_hsa_circ_359646,RMVar_hsa_circ_72951,RMVar_hsa_circ_350851,RMVar_hsa_circ_364249,RMVar_hsa_circ_161048,RMVar_hsa_circ_365822,RMVar_hsa_circ_361027,RMVar_hsa_circ_343482,RMVar_hsa_circ_161050,RMVar_hsa_circ_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161051,RMVar_hsa_circ_161052,RMVar_hsa_circ_353605,RMVar_hsa_circ_45437,RMVar_hsa_circ_18786,RMVar_hsa_circ_374794,RMVar_hsa_circ_339671,RMVar_hsa_circ_344769,RMVar_hsa_circ_310239,RMVar_hsa_circ_161053,RMVar_hsa_circ_161054,RMVar_hsa_circ_161055 92494 RMVar_ID_92494 Human_SNP_ID_518640387 m1A Human chr12 + 122361068 122361068 122361068 TGCGCTTCAGGCTGGCGGACGTGGTCGCCATCACTCGCCTCACTGCGTTGGCCTTGGCTTTGGCT TGCGCTTCAGGCTGGCGGACGTGGTCGCCATCGCTCGCCTCACTGCGTTGGCCTTGGCTTTGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122361017..122361124 26863196 MeRIP-seq:(Medium) rs775992825 Functional Loss SNV dbSNP153 33..33 33 - - - 92495 RMVar_ID_92495 Human_SNP_ID_518644475 m1A Human chr12 - 122377516 122377516 122377516 CATCCCTCAGAAACCATCACAGCCAGCAGCAAAGGAACCTTCAGCTACGCCTCCGATCAGCAACC CATCCCTCAGAAACCATCACAGCCAGCAGCAAGGGAACCTTCAGCTACGCCTCCGATCAGCAACC T C CLIP1 Ensembl:ENSG00000130779 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122377391..122377634 26863196 MeRIP-seq:(Medium) rs746813209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113933,Human_RBP_ID_1789322 Human_miRNA_ID_1422772 RMVar_hsa_circ_360846,RMVar_hsa_circ_357637,RMVar_hsa_circ_364249,RMVar_hsa_circ_161052,RMVar_hsa_circ_54738,RMVar_hsa_circ_33535,RMVar_hsa_circ_39752,RMVar_hsa_circ_294560,RMVar_hsa_circ_161066,RMVar_hsa_circ_161071,RMVar_hsa_circ_161069,RMVar_hsa_circ_289502,RMVar_hsa_circ_285078,RMVar_hsa_circ_161070,RMVar_hsa_circ_321041,RMVar_hsa_circ_300205,RMVar_hsa_circ_161072 92496 RMVar_ID_92496 Human_SNP_ID_518644486 m1A Human chr12 + 122377562 122377562 122377562 TGATGGTTTCTGAGGGATGTTTGAAGGGGTGGAGGGGGAGGAAGACACCATGCTGGCCGTAGAAG TGATGGTTTCTGAGGGATGTTTGAAGGGGTGGGGGGGGAGGAAGACACCATGCTGGCCGTAGAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122377511..122377683 26863196 MeRIP-seq:(Medium) rs7963597 Functional Loss SNV dbSNP153 33..33 33 - - - 92497 RMVar_ID_92497 Human_SNP_ID_518655235 m1A Human chr12 - 122417891 122417891 122417891 AGAGAAAAACATCCTAGGGAGAAGGAAGGAGGAGGCAGGACATTGAAGACTTTCTAGGCTGTAGT AGAGAAAAACATCCTAGGGAGAAGGAAGGAGGCGGCAGGACATTGAAGACTTTCTAGGCTGTAGT T G CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122417889..122418072 26863196 MeRIP-seq:(Medium) rs1198932717 Functional Loss SNV dbSNP153 33..33 33 - - - 92498 RMVar_ID_92498 Human_SNP_ID_518655236 m1A Human chr12 - 122417897 122417897 122417897 GCCCAGAGAGAAAAACATCCTAGGGAGAAGGAAGGAGGAGGCAGGACATTGAAGACTTTCTAGGC GCCCAGAGAGAAAAACATCCTAGGGAGAAGGATGGAGGAGGCAGGACATTGAAGACTTTCTAGGC T A CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122417891..122418057 26863196 MeRIP-seq:(Medium) rs939424047 Functional Loss SNV dbSNP153 33..33 33 - - - 92499 RMVar_ID_92499 Human_SNP_ID_518656408 m1A Human chr12 + 122422570 122422570 122422570 GTCGCCGCCACCTGTCCCACTGCAGCAGCAGCAGCCGCCGCGGCCGCCGCCTCCCGCCTCCCGGC GTCGCCGCCACCTGTCCCACTGCAGCAGCAGCGGCCGCCGCGGCCGCCGCCTCCCGCCTCCCGGC A G CLIP1-AS1 RNACentral:URS00009C32F0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:122422483..122422656;chr12:122422277..122422670 26863196 MeRIP-seq:(Medium) rs1335453315 Functional Loss SNV dbSNP153 33..33 33 - - - 92500 RMVar_ID_92500 Human_SNP_ID_518656556 m1A Human chr12 - 122422802 122422794 122422802 TCCTCCCGGGGCCGCGGTGGGCGCAGACAAAGAGGCGGCGGGGCGGCGCGGGGCCGGGCGCGGGC TCCTCCCGGGGCCGCGGTGGGCGCAGACAAAG________GGGCGGCGCGGGGCCGGGCGCGGGC CCGCCGCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122422751..122422932 26863196 MeRIP-seq:(Medium) rs1160705971 Functional Loss DEL dbSNP153 33..40 33 - - - 92501 RMVar_ID_92501 Human_SNP_ID_518670698 m1A Human chr12 - 122474147 122474147 122474147 CACCCGTCTTCACCCCTCCACTCCCAAAGGGCACCCCGCCGCTGACTCCCAGTGACTCACCCCAG CACCCGTCTTCACCCCTCCACTCCCAAAGGGCTCCCCGCCGCTGACTCCCAGTGACTCACCCCAG T A ZCCHC8 Ensembl:ENSG00000033030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122474099..122474204 26863196 MeRIP-seq:(Medium) rs755245037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810023,Human_RBP_ID_18620319,Human_RBP_ID_26323552,Human_RBP_ID_27419684 92502 RMVar_ID_92502 Human_SNP_ID_518670699 m1A Human chr12 - 122474147 122474147 122474147 CACCCGTCTTCACCCCTCCACTCCCAAAGGGCACCCCGCCGCTGACTCCCAGTGACTCACCCCAG CACCCGTCTTCACCCCTCCACTCCCAAAGGGCCCCCCGCCGCTGACTCCCAGTGACTCACCCCAG T G ZCCHC8 Ensembl:ENSG00000033030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122474099..122474204 26863196 MeRIP-seq:(Medium) rs755245037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810023,Human_RBP_ID_18620319,Human_RBP_ID_26323552,Human_RBP_ID_27419684 92503 RMVar_ID_92503 Human_SNP_ID_518673244 m1A Human chr12 - 122484918 122484918 122484918 GCTCAGTCAGCAAGGAAAGAAGAGAACGGAGAAGCATGTCCTAGAAGACAAGGGAGGAAGATGTT GCTCAGTCAGCAAGGAAAGAAGAGAACGGAGAGGCATGTCCTAGAAGACAAGGGAGGAAGATGTT T C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122484868..122484960 26863196 MeRIP-seq:(Medium) rs190122010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810025,Human_RBP_ID_6145894,Human_RBP_ID_9344772,Human_RBP_ID_11856325,Human_RBP_ID_24543182 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 92504 RMVar_ID_92504 Human_SNP_ID_518673248 m1A Human chr12 - 122484931 122484929 122484931 ACAGAAGAGCGAGGCTCAGTCAGCAAGGAAAGAAGAGAACGGAGAAGCATGTCCTAGAAGACAAG ACAGAAGAGCGAGGCTCAGTCAGCAAGGAAAG__GAGAACGGAGAAGCATGTCCTAGAAGACAAG CTT C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122484881..122485030 26863196 MeRIP-seq:(Medium) rs1353589762 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_810025,Human_RBP_ID_9344772,Human_RBP_ID_11856325,Human_RBP_ID_24543182 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 92505 RMVar_ID_92505 Human_SNP_ID_518677022 m1A Human chr12 - 122500725 122500725 122500725 CACTCGCTTCAAGGACGACGACGGCGACGAGGAGGACGAAAATGGGGTCGGCGACGCGGAGCTAC CACTCGCTTCAAGGACGACGACGGCGACGAGGTGGACGAAAATGGGGTCGGCGACGCGGAGCTAC T A ZCCHC8 Ensembl:ENSG00000033030 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122500677..122500806 26863196 MeRIP-seq:(Medium) rs1468036472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36301,Human_RBP_ID_229603,Human_RBP_ID_9365751,Human_RBP_ID_11856717,Human_RBP_ID_26902751,Human_RBP_ID_27806140 92506 RMVar_ID_92506 Human_SNP_ID_518682515 m1A Human chr12 - 122517367 122517367 122517367 AAGTCTCGATCCAGGAGTAGGGAGCGGAAGAAATCGAGATCCAGAAGCAGAGAGAGGAAGAAATC AAGTCTCGATCCAGGAGTAGGGAGCGGAAGAAGTCGAGATCCAGAAGCAGAGAGAGGAAGAAATC T C RSRC2 Ensembl:ENSG00000111011 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122517177..122517467 26863196 MeRIP-seq:(Medium) rs1443757883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228653,Human_RBP_ID_5554766,Human_RBP_ID_6146122,Human_RBP_ID_9365754,Human_RBP_ID_9668239,Human_RBP_ID_22736954,Human_RBP_ID_22910919,Human_RBP_ID_24543195,Human_RBP_ID_26322235,Human_RBP_ID_27807332 Human_Splice_Rec_1437364,Human_Splice_Rec_1437384,Human_Splice_Rec_1437404,Human_Splice_Rec_1437422,Human_Splice_Rec_1437452,Human_Splice_Rec_1437468,Human_Splice_Rec_1437476,Human_Splice_Rec_1437496,Human_Splice_Rec_1437508,Human_Splice_Rec_1437516 RMVar_hsa_circ_72827,RMVar_hsa_circ_356319,RMVar_hsa_circ_367831,RMVar_hsa_circ_38546,RMVar_hsa_circ_330603,RMVar_hsa_circ_56997,RMVar_hsa_circ_356489,RMVar_hsa_circ_298882,RMVar_hsa_circ_161084,RMVar_hsa_circ_161085 92507 RMVar_ID_92507 Human_SNP_ID_518682998 m1A Human chr12 - 122518877 122518877 122518877 GACAGGCACAAACGCAAAGAAAGAAAGTCATCAAGAGGCAGAAGTCACTCAAGATCTAGGTCTCG GACAGGCACAAACGCAAAGAAAGAAAGTCATCCAGAGGCAGAAGTCACTCAAGATCTAGGTCTCG T G RSRC2 Ensembl:ENSG00000111011 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122518800..122518877 26863196 MeRIP-seq:(Medium) rs551445445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33850,Human_RBP_ID_228328,Human_RBP_ID_811066,Human_RBP_ID_875329,Human_RBP_ID_2310080,Human_RBP_ID_6146130,Human_RBP_ID_9012532,Human_RBP_ID_19059574,Human_RBP_ID_22910637,Human_RBP_ID_24543198,Human_RBP_ID_26321035,Human_RBP_ID_27806152 Human_Splice_Rec_1437363,Human_Splice_Rec_1437383,Human_Splice_Rec_1437403,Human_Splice_Rec_1437421,Human_Splice_Rec_1437451,Human_Splice_Rec_1437467,Human_Splice_Rec_1437475,Human_Splice_Rec_1437495,Human_Splice_Rec_1437507,Human_Splice_Rec_1437515 Human_miRNA_ID_1688891,Human_miRNA_ID_2376611,Human_miRNA_ID_2865787,Human_miRNA_ID_3032260 RMVar_hsa_circ_54145,RMVar_hsa_circ_72827,RMVar_hsa_circ_356319,RMVar_hsa_circ_367831,RMVar_hsa_circ_38546,RMVar_hsa_circ_330603,RMVar_hsa_circ_56997,RMVar_hsa_circ_356489,RMVar_hsa_circ_161084,RMVar_hsa_circ_161085,RMVar_hsa_circ_64979 92508 RMVar_ID_92508 Human_SNP_ID_518684017 m1A Human chr12 - 122522296 122522296 122522296 ACTTTAATCATTTGTTTTTAAACTTTTAGGCTAGTGATACAGAGCGAGATGGACTAGCCCCAGAA ACTTTAATCATTTGTTTTTAAACTTTTAGGCTCGTGATACAGAGCGAGATGGACTAGCCCCAGAA T G RSRC2 Ensembl:ENSG00000111011 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122522251..122522300 26863196 MeRIP-seq:(Medium) rs753268862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24942412 Human_Splice_Rec_1437358,Human_Splice_Rec_1437376,Human_Splice_Rec_1437396,Human_Splice_Rec_1437416,Human_Splice_Rec_1437446,Human_Splice_Rec_1437488,Human_Splice_Rec_1437504,Human_Splice_Rec_1437520,Human_Splice_Rec_1437542,Human_Splice_Rec_1437552 RMVar_hsa_circ_54145,RMVar_hsa_circ_72827,RMVar_hsa_circ_356319,RMVar_hsa_circ_330603,RMVar_hsa_circ_161085,RMVar_hsa_circ_34303,RMVar_hsa_circ_74106,RMVar_hsa_circ_350093 92509 RMVar_ID_92509 Human_SNP_ID_518685576 m1A Human chr12 + 122526861 122526861 122526861 ACTCAGATTCGGTACCTACCGCCATAGTTCAGAGTCCCGGCCGCTAGAGCGGCGCCTCCACTTGT ACTCAGATTCGGTACCTACCGCCATAGTTCAGGGTCCCGGCCGCTAGAGCGGCGCCTCCACTTGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122526851..122526950 32194978 MeRIP-seq:(Medium) rs1264189296 Functional Loss SNV dbSNP153 33..33 33 - - - 92510 RMVar_ID_92510 Human_SNP_ID_518685612 m1A Human chr12 - 122526897 122526897 122526897 GGCGAAGCTTCGGAGCGGCCGGTACTGTTGAAAGCGACAAGTGGAGGCGCCGCTCTAGCGGCCGG GGCGAAGCTTCGGAGCGGCCGGTACTGTTGAATGCGACAAGTGGAGGCGCCGCTCTAGCGGCCGG T A RSRC2 Ensembl:ENSG00000111011 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122526687..122526975 26863196 MeRIP-seq:(Medium) rs1258597258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36481,Human_RBP_ID_1466664,Human_RBP_ID_4247099,Human_RBP_ID_5139743,Human_RBP_ID_5554769,Human_RBP_ID_6146280,Human_RBP_ID_9322792,Human_RBP_ID_9365756,Human_RBP_ID_11857460,Human_RBP_ID_18417357,Human_RBP_ID_18635638,Human_RBP_ID_19057052,Human_RBP_ID_22910638 Human_Splice_Rec_1437357,Human_Splice_Rec_1437375,Human_Splice_Rec_1437395,Human_Splice_Rec_1437445,Human_Splice_Rec_1437461,Human_Splice_Rec_1437487,Human_Splice_Rec_1437503,Human_Splice_Rec_1437511,Human_Splice_Rec_1437517,Human_Splice_Rec_1437541,Human_Splice_Rec_1437547,Human_Splice_Rec_1437557 92511 RMVar_ID_92511 Human_SNP_ID_518685619 m1A Human chr12 + 122526904 122526904 122526904 CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACAGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACCGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122526826..122526975 26863196 MeRIP-seq:(Medium) rs764931238 Functional Loss SNV dbSNP153 33..33 33 - - - 92512 RMVar_ID_92512 Human_SNP_ID_518685620 m1A Human chr12 + 122526904 122526904 122526904 CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACAGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACGGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122526826..122526975 26863196 MeRIP-seq:(Medium) rs764931238 Functional Loss SNV dbSNP153 33..33 33 - - - 92513 RMVar_ID_92513 Human_SNP_ID_518685621 m1A Human chr12 + 122526904 122526904 122526904 CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACAGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT CTAGAGCGGCGCCTCCACTTGTCGCTTTCAACTGTACCGGCCGCTCCGAAGCTTCGCCTCAGACT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122526826..122526975 26863196 MeRIP-seq:(Medium) rs764931238 Functional Loss SNV dbSNP153 33..33 33 - - - 92514 RMVar_ID_92514 Human_SNP_ID_518685633 m1A Human chr12 - 122526916 122526916 122526916 CGCGAGCGATTTAGTCTGAGGCGAAGCTTCGGAGCGGCCGGTACTGTTGAAAGCGACAAGTGGAG CGCGAGCGATTTAGTCTGAGGCGAAGCTTCGGTGCGGCCGGTACTGTTGAAAGCGACAAGTGGAG T A RSRC2 Ensembl:ENSG00000111011 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122526819..122526975 26863196 MeRIP-seq:(Medium) rs896941801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36481,Human_RBP_ID_754605,Human_RBP_ID_1466664,Human_RBP_ID_4247099,Human_RBP_ID_6146280,Human_RBP_ID_9322792,Human_RBP_ID_9365756,Human_RBP_ID_11857460,Human_RBP_ID_18417357,Human_RBP_ID_18620393,Human_RBP_ID_22910638,Human_RBP_ID_23544016 Human_Splice_Rec_1437357,Human_Splice_Rec_1437375,Human_Splice_Rec_1437395,Human_Splice_Rec_1437445,Human_Splice_Rec_1437461,Human_Splice_Rec_1437487,Human_Splice_Rec_1437503,Human_Splice_Rec_1437511,Human_Splice_Rec_1437517,Human_Splice_Rec_1437541,Human_Splice_Rec_1437547,Human_Splice_Rec_1437557 92515 RMVar_ID_92515 Human_SNP_ID_518685634 m1A Human chr12 - 122526916 122526916 122526916 CGCGAGCGATTTAGTCTGAGGCGAAGCTTCGGAGCGGCCGGTACTGTTGAAAGCGACAAGTGGAG CGCGAGCGATTTAGTCTGAGGCGAAGCTTCGGGGCGGCCGGTACTGTTGAAAGCGACAAGTGGAG T C RSRC2 Ensembl:ENSG00000111011 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122526819..122526975 26863196 MeRIP-seq:(Medium) rs896941801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36481,Human_RBP_ID_754605,Human_RBP_ID_1466664,Human_RBP_ID_4247099,Human_RBP_ID_6146280,Human_RBP_ID_9322792,Human_RBP_ID_9365756,Human_RBP_ID_11857460,Human_RBP_ID_18417357,Human_RBP_ID_18620393,Human_RBP_ID_22910638,Human_RBP_ID_23544016 Human_Splice_Rec_1437357,Human_Splice_Rec_1437375,Human_Splice_Rec_1437395,Human_Splice_Rec_1437445,Human_Splice_Rec_1437461,Human_Splice_Rec_1437487,Human_Splice_Rec_1437503,Human_Splice_Rec_1437511,Human_Splice_Rec_1437517,Human_Splice_Rec_1437541,Human_Splice_Rec_1437547,Human_Splice_Rec_1437557 92516 RMVar_ID_92516 Human_SNP_ID_518685640 m1A Human chr12 + 122526921 122526921 122526921 CTTGTCGCTTTCAACAGTACCGGCCGCTCCGAAGCTTCGCCTCAGACTAAATCGCTCGCGCGAGA CTTGTCGCTTTCAACAGTACCGGCCGCTCCGAGGCTTCGCCTCAGACTAAATCGCTCGCGCGAGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:122526682..122526975 26863196 MeRIP-seq:(Medium) rs543009224 Functional Loss SNV dbSNP153 33..33 33 - - - 92517 RMVar_ID_92517 Human_SNP_ID_518685813 m1A Human chr12 + 122527315 122527315 122527315 AGGCGGTTGTGTGAGTCAGGAAGAGGGGCCAGATATCTGAGTGTTCCTCTTTAGTTTCTTCAATT AGGCGGTTGTGTGAGTCAGGAAGAGGGGCCAGGTATCTGAGTGTTCCTCTTTAGTTTCTTCAATT A G KNTC1 Ensembl:ENSG00000184445 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122527242..122527441 26863196 MeRIP-seq:(Medium) rs577392947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3396576,Human_RBP_ID_8787447 Human_Splice_Rec_1437559,Human_Splice_Rec_1437561,Human_Splice_Rec_1437637 RMVar_hsa_circ_107161,RMVar_hsa_circ_161088 92518 RMVar_ID_92518 Human_SNP_ID_518685822 m1A Human chr12 + 122527335 122527335 122527335 AAGAGGGGCCAGATATCTGAGTGTTCCTCTTTAGTTTCTTCAATTGCAGGTGAGGACGGGGAGCT AAGAGGGGCCAGATATCTGAGTGTTCCTCTTTGGTTTCTTCAATTGCAGGTGAGGACGGGGAGCT A G KNTC1 Ensembl:ENSG00000184445 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122527284..122527385 26863196 MeRIP-seq:(Medium) rs1481531241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18410936 Human_Splice_Rec_1437559,Human_Splice_Rec_1437561,Human_Splice_Rec_1437637 RMVar_hsa_circ_107161,RMVar_hsa_circ_161088 92519 RMVar_ID_92519 Human_SNP_ID_518746350 m1A Human chr12 - 122753684 122753684 122753684 AATGTCAGCAGCCATTTCACAAACCTGTAAGCAAGGAAAATAACACACCCTCACTATTTTAGAAT AATGTCAGCAGCCATTTCACAAACCTGTAAGCGAGGAAAATAACACACCCTCACTATTTTAGAAT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:122753676..122753775 26863196 MeRIP-seq:(Medium) rs749388565 Functional Loss SNV dbSNP153 33..33 33 - - - 92520 RMVar_ID_92520 Human_SNP_ID_518746370 m1A Human chr12 + 122753746 122753746 122753746 ATTTCTGAATCCAGCGGGGCTGACTGCAAAGGAGACCCAAGGAACAGTGCCAAGTTAGATGCCGA ATTTCTGAATCCAGCGGGGCTGACTGCAAAGGCGACCCAAGGAACAGTGCCAAGTTAGATGCCGA A C DENR Ensembl:ENSG00000139726 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr12:122753648..122753825;chr12:122753660..122753775;chr12:122753676..122753800 26863196,32194978 MeRIP-seq:(Medium) rs1240744117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754886,Human_RBP_ID_1466775,Human_RBP_ID_1789582,Human_RBP_ID_4247102,Human_RBP_ID_11859725,Human_RBP_ID_23544171 Human_Splice_Rec_1437884,Human_Splice_Rec_1437896,Human_Splice_Rec_1437908,Human_Splice_Rec_1437912 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 92521 RMVar_ID_92521 Human_SNP_ID_518767373 m1A Human chr12 + 122835517 122835517 122835517 GCTGCCGGACCGTGAGGCTGTGAGTCGCGCGGACGGAGCCGGACAAAAGCGGGCGGCGGCGGCAG GCTGCCGGACCGTGAGGCTGTGAGTCGCGCGGGCGGAGCCGGACAAAAGCGGGCGGCGGCGGCAG A G HIP1R Ensembl:ENSG00000130787 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122835467..122835675 26863196 MeRIP-seq:(Medium) rs1413007510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247103 RMVar_hsa_circ_84373,RMVar_hsa_circ_161197 92522 RMVar_ID_92522 Human_SNP_ID_518772554 m1A Human chr12 + 122854094 122854094 122854094 GGCCATCGCCGTATCCCAGATGTCCTCAGGCCAGTGCCGCCTGGCCCCCCTCATCCAGGTCATCC GGCCATCGCCGTATCCCAGATGTCCTCAGGCCGGTGCCGCCTGGCCCCCCTCATCCAGGTCATCC A G HIP1R Ensembl:ENSG00000130787 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122853687..122854150 32194978 MeRIP-seq:(Medium) rs1332627553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1438028,Human_Splice_Rec_1438029,Human_Splice_Rec_1438060,Human_Splice_Rec_1438061,Human_Splice_Rec_1438120,Human_Splice_Rec_1438121,Human_Splice_Rec_1438144,Human_Splice_Rec_1438145,Human_Splice_Rec_1438151 RMVar_hsa_circ_43947,RMVar_hsa_circ_25718,RMVar_hsa_circ_80778,RMVar_hsa_circ_161200,RMVar_hsa_circ_100123,RMVar_hsa_circ_161201,RMVar_hsa_circ_161204 92523 RMVar_ID_92523 Human_SNP_ID_518773672 m1A Human chr12 + 122856535 122856535 122856535 GCTGGCCTTCCAGGTGGAGCAGGTGAAGCGGGAGTCGGAGTTGAAGGTATGTCCCTTGTGGCACA GCTGGCCTTCCAGGTGGAGCAGGTGAAGCGGGGGTCGGAGTTGAAGGTATGTCCCTTGTGGCACA A G HIP1R Ensembl:ENSG00000130787 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122855986..122857261 26863196 MeRIP-seq:(Medium) rs1381384318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753595,Human_RBP_ID_5521871,Human_RBP_ID_26777547,Human_RBP_ID_27807353 Human_Splice_Rec_1438045,Human_Splice_Rec_1438077,Human_Splice_Rec_1438137 RMVar_hsa_circ_80778,RMVar_hsa_circ_161200,RMVar_hsa_circ_100123,RMVar_hsa_circ_79317,RMVar_hsa_circ_161204,RMVar_hsa_circ_102953,RMVar_hsa_circ_161205,RMVar_hsa_circ_161206,RMVar_hsa_circ_82163,RMVar_hsa_circ_161207 92524 RMVar_ID_92524 Human_SNP_ID_518773925 m1A Human chr12 + 122857104 122857104 122857104 GCTCTGAGTGGAGCTGTGCGGCAGCGGGAGGCAGACCTGCTGGCGGCGCAGAGCCTGGTGCGCGA GCTCTGAGTGGAGCTGTGCGGCAGCGGGAGGCCGACCTGCTGGCGGCGCAGAGCCTGGTGCGCGA A C HIP1R Ensembl:ENSG00000130787 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122857025..122857200 26863196 MeRIP-seq:(Medium) rs1229959272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18976419 Human_Splice_Rec_1438048,Human_Splice_Rec_1438080,Human_Splice_Rec_1438140 RMVar_hsa_circ_80778,RMVar_hsa_circ_161200,RMVar_hsa_circ_100123,RMVar_hsa_circ_79317,RMVar_hsa_circ_161204,RMVar_hsa_circ_102953,RMVar_hsa_circ_161205,RMVar_hsa_circ_161206,RMVar_hsa_circ_82163,RMVar_hsa_circ_161207 92525 RMVar_ID_92525 Human_SNP_ID_518774397 m1A Human chr12 - 122858388 122858388 122858388 GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCACGGCATCCAAGGCCTCCTGGGCCCTGCTCACC GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCTCGGCATCCAAGGCCTCCTGGGCCCTGCTCACC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122858005..122860203 32194978 MeRIP-seq:(Medium) rs773821606 Functional Loss SNV dbSNP153 33..33 33 - - - 92526 RMVar_ID_92526 Human_SNP_ID_518774398 m1A Human chr12 - 122858388 122858388 122858388 GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCACGGCATCCAAGGCCTCCTGGGCCCTGCTCACC GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCGCGGCATCCAAGGCCTCCTGGGCCCTGCTCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122858005..122860203 32194978 MeRIP-seq:(Medium) rs773821606 Functional Loss SNV dbSNP153 33..33 33 - - - 92527 RMVar_ID_92527 Human_SNP_ID_518774399 m1A Human chr12 - 122858388 122858388 122858388 GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCACGGCATCCAAGGCCTCCTGGGCCCTGCTCACC GGTACTGGGCGTGGCCCTCCTCCAGGGTGCTCCCGGCATCCAAGGCCTCCTGGGCCCTGCTCACC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122858005..122860203 32194978 MeRIP-seq:(Medium) rs773821606 Functional Loss SNV dbSNP153 33..33 33 - - - 92528 RMVar_ID_92528 Human_SNP_ID_518775246 m1A Human chr12 + 122860202 122860194 122860203 CATCCACTAGCCTGCAGAAGGAGATCGTGGAGAGCGGCAGGGTGAGGGGCCGGCGGCAGCAGGGC CATCCACTAGCCTGCAGAAGGAGAT_________CGGCAGGGTGAGGGGCCGGCGGCAGCAGGGC TCGTGGAGAG T HIP1R Ensembl:ENSG00000130787 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122859139..122860203 26863196 MeRIP-seq:(Medium) rs1284882892 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_3943765,Human_RBP_ID_19057072 Human_Splice_Rec_1438096,Human_Splice_Rec_1438097,Human_Splice_Rec_1438175,Human_Splice_Rec_1438187,Human_Splice_Rec_1438193 RMVar_hsa_circ_80778,RMVar_hsa_circ_161200,RMVar_hsa_circ_100123,RMVar_hsa_circ_161204,RMVar_hsa_circ_161209,RMVar_hsa_circ_90699,RMVar_hsa_circ_111474,RMVar_hsa_circ_161208,RMVar_hsa_circ_374427,RMVar_hsa_circ_161210 92529 RMVar_ID_92529 Human_SNP_ID_518775860 m1A Human chr12 - 122861398 122861398 122861398 CCGGATGGCCACCTCCTCTCCAGGGCTGCCTGATGCCCCAGCCAGCACGTAGTGTTGCTTCCGCA CCGGATGGCCACCTCCTCTCCAGGGCTGCCTGGTGCCCCAGCCAGCACGTAGTGTTGCTTCCGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122861312..122861561 32194978 MeRIP-seq:(Medium) rs753115161 Functional Loss SNV dbSNP153 33..33 33 - - - 92530 RMVar_ID_92530 Human_SNP_ID_518775865 m1A Human chr12 + 122861417 122861417 122861417 GCTGGCTGGGGCATCAGGCAGCCCTGGAGAGGAGGTGGCCATCCGGCCCAGCACTGCCCCCCGAA GCTGGCTGGGGCATCAGGCAGCCCTGGAGAGGTGGTGGCCATCCGGCCCAGCACTGCCCCCCGAA A T HIP1R Ensembl:ENSG00000130787 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122861367..122861465 26863196 MeRIP-seq:(Medium) rs779185355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1438107,Human_Splice_Rec_1438185,Human_Splice_Rec_1438201 Human_miRNA_ID_2016335,Human_miRNA_ID_2675399,Human_miRNA_ID_2926150 RMVar_hsa_circ_80778,RMVar_hsa_circ_161200,RMVar_hsa_circ_100123,RMVar_hsa_circ_161204,RMVar_hsa_circ_90699,RMVar_hsa_circ_161210,RMVar_hsa_circ_267728 92531 RMVar_ID_92531 Human_SNP_ID_518777512 m1A Human chr12 + 122865626 122865626 122865626 TACAGCTTCATTTCCTTTAAGAAAACAGTTACAGTAGAGTTCAAGTCCGAGAGCAGGAATGTACG TACAGCTTCATTTCCTTTAAGAAAACAGTTACTGTAGAGTTCAAGTCCGAGAGCAGGAATGTACG A T AC027290.2 Ensembl:ENSG00000256152 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:122865575..122865725 32194978 MeRIP-seq:(Medium) rs1049852413 Functional Loss SNV dbSNP153 33..33 33 - - - 92532 RMVar_ID_92532 Human_SNP_ID_518778098 m1A Human chr12 - 122867295 122867295 122867295 CGGGACGCTTAGCCACCCCGTTTACTGCGGCCATGAGTTCGGGACAGGCCGTGCCGTACCCAGGA CGGGACGCTTAGCCACCCCGTTTACTGCGGCCGTGAGTTCGGGACAGGCCGTGCCGTACCCAGGA T C VPS37B Ensembl:ENSG00000139722 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122867246..122867494 26863196 MeRIP-seq:(Medium) rs1475121878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17683656 92533 RMVar_ID_92533 Human_SNP_ID_518778101 m1A Human chr12 + 122867302 122867302 122867302 TACGGCACGGCCTGTCCCGAACTCATGGCCGCAGTAAACGGGGTGGCTAAGCGTCCCGCAGGCAC TACGGCACGGCCTGTCCCGAACTCATGGCCGCGGTAAACGGGGTGGCTAAGCGTCCCGCAGGCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122867198..122867492 26863196 MeRIP-seq:(Medium) rs1464101858 Functional Loss SNV dbSNP153 33..33 33 - - - 92534 RMVar_ID_92534 Human_SNP_ID_518779422 m1A Human chr12 - 122871909 122871909 122871909 TGAGGTGGCGGCGGCTGGGCTGTGGTAGAGGAAGCCGATCACCAGTGAGTGAAAAGGGAACTAGG TGAGGTGGCGGCGGCTGGGCTGTGGTAGAGGAGGCCGATCACCAGTGAGTGAAAAGGGAACTAGG T C AC027290.3,VPS37B Ensembl:ENSG00000280138,Ensembl:ENSG00000139722 Other,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122871903..122872133 26863196 MeRIP-seq:(Medium) rs1436475651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3422037,Human_RBP_ID_22573737 92535 RMVar_ID_92535 Human_SNP_ID_518783784 m1A Human chr12 - 122889791 122889791 122889791 GCGCCCCATGGTGGTTAATTTAGGAGGAAACAAGGAGCTTCGTGATGATTTTGGAGCAGAGAAGC GCGCCCCATGGTGGTTAATTTAGGAGGAAACAGGGAGCTTCGTGATGATTTTGGAGCAGAGAAGC T C VPS37B Ensembl:ENSG00000139722 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:122889788..122889921 26863196 MeRIP-seq:(Medium) rs996865796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6147263,Human_RBP_ID_11861342 92536 RMVar_ID_92536 Human_SNP_ID_518785055 m1A Human chr12 + 122895036 122895036 122895036 GCAACCCTTACAGAAAAACGTATCCTGTCGCCACCCTTAGGCCCATCCACGAACTCCCGTAACTC GCAACCCTTACAGAAAAACGTATCCTGTCGCCTCCCTTAGGCCCATCCACGAACTCCCGTAACTC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122895012..122895132 32194978 MeRIP-seq:(Medium) rs1182661172 Functional Loss SNV dbSNP153 33..33 33 - - - 92537 RMVar_ID_92537 Human_SNP_ID_518785278 m1A Human chr12 - 122895956 122895956 122895956 GGGCCAGCTGACGGAGATGGTGCAGAAGATGGAGGAGGTGAGCCGAGCTGGGCTTAAGGCGGCGG GGGCCAGCTGACGGAGATGGTGCAGAAGATGGTGGAGGTGAGCCGAGCTGGGCTTAAGGCGGCGG T A VPS37B Ensembl:ENSG00000139722 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:122895953..122896100 26863196 MeRIP-seq:(Medium) rs762249308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709967 Human_Splice_Rec_1438205,Human_Splice_Rec_1438211 92538 RMVar_ID_92538 Human_SNP_ID_518785332 m1A Human chr12 + 122896067 122896067 122896067 ACCGGGCTTCGCTCCCGGCGCCCGCCATCCCCACGTCTCGGCCGTCGTCGCCACCGCCGCTGCGG ACCGGGCTTCGCTCCCGGCGCCCGCCATCCCCGCGTCTCGGCCGTCGTCGCCACCGCCGCTGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:122895180..122896125;chr12:122895163..122896125;chr12:122895763..122896125 26863196 MeRIP-seq:(Medium) rs1457873750 Functional Loss SNV dbSNP153 33..33 33 - - - 92539 RMVar_ID_92539 Human_SNP_ID_518799084 m1A Human chr12 - 122950432 122950432 122950432 CTGGCCATTGGCAGGTAGCTGGCTCAACCCCCACGCCCTGCCCCGCACACCCCGACCTGCACCAG CTGGCCATTGGCAGGTAGCTGGCTCAACCCCCGCGCCCTGCCCCGCACACCCCGACCTGCACCAG T C ABCB9 Ensembl:ENSG00000150967 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122950429..122950512 26863196 MeRIP-seq:(Medium) rs1294654780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24072,RMVar_hsa_circ_294867,RMVar_hsa_circ_104417,RMVar_hsa_circ_161219,RMVar_hsa_circ_334428,RMVar_hsa_circ_161220,RMVar_hsa_circ_277396,RMVar_hsa_circ_161221 92540 RMVar_ID_92540 Human_SNP_ID_518802906 m1A Human chr12 + 122966372 122966372 122966372 CTGGGGTGCAGTTTCCGCGCTGCTCATTGAAGACTGCGCCGGACGCGGTCCTCGCTCCGCTCTTC CTGGGGTGCAGTTTCCGCGCTGCTCATTGAAGGCTGCGCCGGACGCGGTCCTCGCTCCGCTCTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122966257..122966414 26863196 MeRIP-seq:(Medium) rs986228011 Functional Loss SNV dbSNP153 33..33 33 - - - 92541 RMVar_ID_92541 Human_SNP_ID_518805264 m1A Human chr12 - 122975315 122975315 122975315 GAAGCGCACGTGCAGCCCATAGCGCGCCACGTACAAGTTATCGGTGCAGAAGCAGGCGCAGCGGC GAAGCGCACGTGCAGCCCATAGCGCGCCACGTCCAAGTTATCGGTGCAGAAGCAGGCGCAGCGGC T G ABCB9 Ensembl:ENSG00000150967 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:122975267..122975846 26863196 MeRIP-seq:(Medium) rs1238866409 Functional Loss SNV dbSNP153 33..33 33 - - - 92542 RMVar_ID_92542 Human_SNP_ID_518805778 m1A Human chr12 + 122976710 122976710 122976710 CAGCGGCTGGGGCAGGAGTCAGCAGCTAGGAAAGCCCTCATCGCGAGTTCCTACCACCCGGCACG CAGCGGCTGGGGCAGGAGTCAGCAGCTAGGAAGGCCCTCATCGCGAGTTCCTACCACCCGGCACG A G OGFOD2,AC026362.1 Ensembl:ENSG00000111325,Ensembl:ENSG00000256028 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122976624..122976747 26863196 MeRIP-seq:(Medium) rs761260271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942363,Human_RBP_ID_4248435,Human_RBP_ID_26609351 Human_Splice_Rec_1438504,Human_Splice_Rec_1438505,Human_Splice_Rec_1438514,Human_Splice_Rec_1438515,Human_Splice_Rec_1438524,Human_Splice_Rec_1438525,Human_Splice_Rec_1438536,Human_Splice_Rec_1438537,Human_Splice_Rec_1438547,Human_Splice_Rec_1438559,Human_Splice_Rec_1438572,Human_Splice_Rec_1438573,Human_Splice_Rec_1438584,Human_Splice_Rec_1438585,Human_Splice_Rec_1438596,Human_Splice_Rec_1438597,Human_Splice_Rec_1438607,Human_Splice_Rec_1438616,Human_Splice_Rec_1438617,Human_Splice_Rec_1438624,Human_Splice_Rec_1438625,Human_Splice_Rec_1438638,Human_Splice_Rec_1438639,Human_Splice_Rec_1438650,Human_Splice_Rec_1438651,Human_Splice_Rec_1438665,Human_Splice_Rec_1438670,Human_Splice_Rec_1438671,Human_Splice_Rec_1438678,Human_Splice_Rec_1438679,Human_Splice_Rec_1438692,Human_Splice_Rec_1438693,Human_Splice_Rec_1438701,Human_Splice_Rec_1438714,Human_Splice_Rec_1438715,Human_Splice_Rec_1438721,Human_Splice_Rec_1438742,Human_Splice_Rec_1438743 92543 RMVar_ID_92543 Human_SNP_ID_518806492 m1A Human chr12 + 122978867 122978867 122978867 TGTACCCTGACTGTGGCGGGGGCCGGCTCGACAGCCACCGGGCCTTTGTGGTCAAATACGCACCG TGTACCCTGACTGTGGCGGGGGCCGGCTCGACGGCCACCGGGCCTTTGTGGTCAAATACGCACCG A G OGFOD2,AC026362.1 Ensembl:ENSG00000111325,Ensembl:ENSG00000256028 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122978817..122978962 26863196 MeRIP-seq:(Medium) rs926326073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087494,Human_RBP_ID_9367125,Human_RBP_ID_22040174 92544 RMVar_ID_92544 Human_SNP_ID_518806801 m1A Human chr12 - 122979399 122979399 122979399 GGCTGCGGGGATTTTATTTCTGCCCCCAGACCAAGGCAACGGAGCCCTCACCTGCCTGCCACCCC GGCTGCGGGGATTTTATTTCTGCCCCCAGACCGAGGCAACGGAGCCCTCACCTGCCTGCCACCCC T C ABCB9 Ensembl:ENSG00000150967 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122979131..122979798 26863196 MeRIP-seq:(Medium) rs1384357600 Functional Loss SNV dbSNP153 33..33 33 - - - 92545 RMVar_ID_92545 Human_SNP_ID_518807261 m1A Human chr12 - 122980741 122980741 122980741 GGGGCCCCCGGGGCTGCTCCGTTCCCACCTCGACCGCCCTGCGGGCCGGACAGCCCGCCCCGCGC GGGGCCCCCGGGGCTGCTCCGTTCCCACCTCGTCCGCCCTGCGGGCCGGACAGCCCGCCCCGCGC T A ABCB9 Ensembl:ENSG00000150967 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:122980701..122980775 26863410 MeRIP-seq:(Medium) rs1463849992 Functional Loss SNV dbSNP153 33..33 33 - - - 92546 RMVar_ID_92546 Human_SNP_ID_518807453 m1A Human chr12 + 122981219 122981219 122981219 CCGGGGACGGGGGTCGGAAAAGAGAAAGAAGAAGAGCAGGAAAGACACCTCGAGGAACTGCTCGG CCGGGGACGGGGGTCGGAAAAGAGAAAGAAGAGGAGCAGGAAAGACACCTCGAGGAACTGCTCGG A G ARL6IP4,AC026362.1 Ensembl:ENSG00000182196,Ensembl:ENSG00000256028 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:122980299..122981449;chr12:122980299..122981499 26863196 MeRIP-seq:(Medium) rs1291630884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875355,Human_RBP_ID_3421757,Human_RBP_ID_4248314,Human_RBP_ID_5094097,Human_RBP_ID_5558906,Human_RBP_ID_5645388,Human_RBP_ID_9365774,Human_RBP_ID_22900202 Human_Splice_Rec_1438752,Human_Splice_Rec_1438753,Human_Splice_Rec_1438762,Human_Splice_Rec_1438763,Human_Splice_Rec_1438772,Human_Splice_Rec_1438773,Human_Splice_Rec_1438782,Human_Splice_Rec_1438783,Human_Splice_Rec_1438792,Human_Splice_Rec_1438793,Human_Splice_Rec_1438798,Human_Splice_Rec_1438799,Human_Splice_Rec_1438806,Human_Splice_Rec_1438807,Human_Splice_Rec_1438814,Human_Splice_Rec_1438815,Human_Splice_Rec_1438824,Human_Splice_Rec_1438825,Human_Splice_Rec_1438834,Human_Splice_Rec_1438840,Human_Splice_Rec_1438841,Human_Splice_Rec_1438848,Human_Splice_Rec_1438849,Human_Splice_Rec_1438858,Human_Splice_Rec_1438861,Human_Splice_Rec_1438870,Human_Splice_Rec_1438876,Human_Splice_Rec_1438877,Human_Splice_Rec_1438886,Human_Splice_Rec_1438891,Human_Splice_Rec_1438897 RMVar_hsa_circ_40126,RMVar_hsa_circ_113283,RMVar_hsa_circ_378741,RMVar_hsa_circ_161223,RMVar_hsa_circ_41806,RMVar_hsa_circ_161224 92547 RMVar_ID_92547 Human_SNP_ID_518807798 m1A Human chr12 + 122981800 122981800 122981800 AAGCTGAAGAAGAAGGGCAAGGAGAAGGCGGAAGCACAGCAGGTGGAGGCTCTGCCGGGCCCCTC AAGCTGAAGAAGAAGGGCAAGGAGAAGGCGGAGGCACAGCAGGTGGAGGCTCTGCCGGGCCCCTC A G ARL6IP4,AC026362.1 Ensembl:ENSG00000182196,Ensembl:ENSG00000256028 Protein coding,lincRNA CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122981751..122981825 32194978 MeRIP-seq:(Medium) rs1279839076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_195028,Human_RBP_ID_228291,Human_RBP_ID_875356,Human_RBP_ID_1479648,Human_RBP_ID_5094099,Human_RBP_ID_5111833,Human_RBP_ID_5645280,Human_RBP_ID_9323306,Human_RBP_ID_9365776,Human_RBP_ID_17650247,Human_RBP_ID_18976428,Human_RBP_ID_24366150,Human_RBP_ID_24543342,Human_RBP_ID_26322260,Human_RBP_ID_27806190 Human_Splice_Rec_1438747,Human_Splice_Rec_1438755,Human_Splice_Rec_1438765,Human_Splice_Rec_1438775,Human_Splice_Rec_1438785,Human_Splice_Rec_1438795,Human_Splice_Rec_1438801,Human_Splice_Rec_1438809,Human_Splice_Rec_1438817,Human_Splice_Rec_1438827,Human_Splice_Rec_1438835,Human_Splice_Rec_1438843,Human_Splice_Rec_1438851,Human_Splice_Rec_1438859,Human_Splice_Rec_1438863,Human_Splice_Rec_1438871,Human_Splice_Rec_1438879,Human_Splice_Rec_1438887,Human_Splice_Rec_1438893,Human_Splice_Rec_1438899 RMVar_hsa_circ_40126,RMVar_hsa_circ_113283,RMVar_hsa_circ_378741,RMVar_hsa_circ_161223,RMVar_hsa_circ_64350,RMVar_hsa_circ_161224 92548 RMVar_ID_92548 Human_SNP_ID_518837801 m1A Human chr12 - 123110487 123110487 123110487 ACCTCCTCTCCCATTGTGCTTCTCCCTGCAGGATGCTGGCACGTGTGTCCTGGTCCTCAACAACC ACCTCCTCTCCCATTGTGCTTCTCCCTGCAGGTTGCTGGCACGTGTGTCCTGGTCCTCAACAACC T A PITPNM2 Ensembl:ENSG00000090975 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:123110448..123110529;chr12:123110438..123110549 26863196 MeRIP-seq:(Medium) rs1223669086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1439094 RMVar_hsa_circ_161235,RMVar_hsa_circ_374963,RMVar_hsa_circ_161234,RMVar_hsa_circ_161236 92549 RMVar_ID_92549 Human_SNP_ID_518846908 m1A Human chr12 - 123150798 123150798 123150798 CCCCGTGAGGCGGCGTGAGGTGGCGGCGGCCCAGCCGGGGCCCCGAAGAGGACAGAGCCCGCGGC CCCCGTGAGGCGGCGTGAGGTGGCGGCGGCCCGGCCGGGGCCCCGAAGAGGACAGAGCCCGCGGC T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123150715..123151107 26863196 MeRIP-seq:(Medium) rs891170619 Functional Loss SNV dbSNP153 33..33 33 - - - 92550 RMVar_ID_92550 Human_SNP_ID_518876573 m1A Human chr12 + 123265218 123265218 123265218 CCGGGCTTACCGCGCTTCAGCCTCTCCATGGCACTCTTGCTCCCTGCGTACGTGGGTCTGATCTC CCGGGCTTACCGCGCTTCAGCCTCTCCATGGCGCTCTTGCTCCCTGCGTACGTGGGTCTGATCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:123265176..123265225 26863196 MeRIP-seq:(Medium) rs1251600299 Functional Loss SNV dbSNP153 33..33 33 - - - 92551 RMVar_ID_92551 Human_SNP_ID_518876891 m1A Human chr12 + 123266239 123266223 123266239 GTCCTGCTCCGGCTGCTCTGCCTCCCCACGGCACTGCCTCCAGGCCTCACGGGCCTCCCGCCTGT GTCCTGCTCCGGCTGCT________________CTGCCTCCAGGCCTCACGGGCCTCCCGCCTGT TCTGCCTCCCCACGGCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123266235..123266319 26863196 MeRIP-seq:(Medium) rs1233141631 Functional Loss DEL dbSNP153 18..33 33 - - - 92552 RMVar_ID_92552 Human_SNP_ID_518876899 m1A Human chr12 + 123266239 123266239 123266239 GTCCTGCTCCGGCTGCTCTGCCTCCCCACGGCACTGCCTCCAGGCCTCACGGGCCTCCCGCCTGT GTCCTGCTCCGGCTGCTCTGCCTCCCCACGGCCCTGCCTCCAGGCCTCACGGGCCTCCCGCCTGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123266235..123266319 26863196 MeRIP-seq:(Medium) rs1284062694 Functional Loss SNV dbSNP153 33..33 33 - - - 92553 RMVar_ID_92553 Human_SNP_ID_518877216 m1A Human chr12 + 123267273 123267273 123267273 AAGACGTTGCCATGCTGGTGGAAGGCGAGTGGACACTCCCAGCTGTGGGGTGGGGAGAGAGAGGC AAGACGTTGCCATGCTGGTGGAAGGCGAGTGGGCACTCCCAGCTGTGGGGTGGGGAGAGAGAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:123267138..123267337;chr12:123267226..123267300 26863196 MeRIP-seq:(Medium) rs146228272 Functional Loss SNV dbSNP153 33..33 33 - - - 92554 RMVar_ID_92554 Human_SNP_ID_518877219 m1A Human chr12 + 123267281 123267280 123267281 GCCATGCTGGTGGAAGGCGAGTGGACACTCCCAGCTGTGGGGTGGGGAGAGAGAGGCCAGGAGTC GCCATGCTGGTGGAAGGCGAGTGGACACTCCC_GCTGTGGGGTGGGGAGAGAGAGGCCAGGAGTC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:123267251..123267300;chr12:123267265..123267351 26863196 MeRIP-seq:(Medium) rs761073337 Functional Loss DEL dbSNP153 33..33 33 - - - 92555 RMVar_ID_92555 Human_SNP_ID_518878592 m1A Human chr12 + 123271489 123271470 123271489 CCCCGCCCCCGGCCTCCGCGGGCGCCCCGGGCATCCCCGGGCCGGGGCCGGGCGCGCGGACCCCC CCCCGCCCCCGGCC___________________TCCCCGGGCCGGGGCCGGGCGCGCGGACCCCC CTCCGCGGGCGCCCCGGGCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:123271487..123271833 26863196 MeRIP-seq:(Medium) rs1463165347 Functional Loss DEL dbSNP153 15..33 33 - - - 92556 RMVar_ID_92556 Human_SNP_ID_518878594 m1A Human chr12 + 123271489 123271479 123271489 CCCCGCCCCCGGCCTCCGCGGGCGCCCCGGGCATCCCCGGGCCGGGGCCGGGCGCGCGGACCCCC CCCCGCCCCCGGCCTCCGCGGGC__________TCCCCGGGCCGGGGCCGGGCGCGCGGACCCCC CGCCCCGGGCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:123271487..123271833 26863196 MeRIP-seq:(Medium) rs1415554424 Functional Loss DEL dbSNP153 24..33 33 - - - 92557 RMVar_ID_92557 Human_SNP_ID_518878595 m1A Human chr12 + 123271489 123271480 123271490 CCCCGCCCCCGGCCTCCGCGGGCGCCCCGGGCATCCCCGGGCCGGGGCCGGGCGCGCGGACCCCC CCCCGCCCCCGGCCTCCGCGGGCG__________CCCCGGGCCGGGGCCGGGCGCGCGGACCCCC GCCCCGGGCAT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:123271487..123271833 26863196 MeRIP-seq:(Medium) rs954857981 Functional Loss DEL dbSNP153 25..34 33 - - - 92558 RMVar_ID_92558 Human_SNP_ID_518878712 m1A Human chr12 + 123271733 123271733 123271733 CTGCAGCCCCGCGCCCGTCCGAGCGCCCGCCGAGCGCCCGCGCACTTTTTGTTGTCGGCGGCTCG CTGCAGCCCCGCGCCCGTCCGAGCGCCCGCCGTGCGCCCGCGCACTTTTTGTTGTCGGCGGCTCG A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:123271631..123271775 26863410 MeRIP-seq:(Medium) rs963341826 Functional Loss SNV dbSNP153 33..33 33 - - - 92559 RMVar_ID_92559 Human_SNP_ID_518878811 m1A Human chr12 - 123271985 123271985 123271985 CGCGCGCGGGCCTCAGGCGCCGCCGGGACCCCAGCCCCCCAAACTTTGGCAAGTTGCGGGCGCCG CGCGCGCGGGCCTCAGGCGCCGCCGGGACCCCCGCCCCCCAAACTTTGGCAAGTTGCGGGCGCCG T G CDK2AP1 Ensembl:ENSG00000111328 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:123271876..123272025 26863410 MeRIP-seq:(Medium) rs895487460 Functional Loss SNV dbSNP153 33..33 33 - - - 92560 RMVar_ID_92560 Human_SNP_ID_518899877 m1A Human chr12 - 123339858 123339858 123339858 TGAAAATAAGCCAGGAAGCTTAGCTTGTAGAAAGAAGTGGGAATAGTAGGTCTGGGCTCCATGGA TGAAAATAAGCCAGGAAGCTTAGCTTGTAGAAGGAAGTGGGAATAGTAGGTCTGGGCTCCATGGA T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123339848..123339959 26863196 MeRIP-seq:(Medium) rs184325891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11864569 RMVar_hsa_circ_7345,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_9389,RMVar_hsa_circ_41035,RMVar_hsa_circ_31067,RMVar_hsa_circ_161318,RMVar_hsa_circ_92146,RMVar_hsa_circ_2491,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161329,RMVar_hsa_circ_161330,RMVar_hsa_circ_323804,RMVar_hsa_circ_66999,RMVar_hsa_circ_161332,RMVar_hsa_circ_80624,RMVar_hsa_circ_37146,RMVar_hsa_circ_77087,RMVar_hsa_circ_161333,RMVar_hsa_circ_70431,RMVar_hsa_circ_4343,RMVar_hsa_circ_13440,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_330338,RMVar_hsa_circ_65931,RMVar_hsa_circ_293777,RMVar_hsa_circ_161337,RMVar_hsa_circ_295963,RMVar_hsa_circ_292683,RMVar_hsa_circ_161339,RMVar_hsa_circ_56723,RMVar_hsa_circ_161340,RMVar_hsa_circ_161338,RMVar_hsa_circ_304795 92561 RMVar_ID_92561 Human_SNP_ID_518907675 m1A Human chr12 - 123364787 123364784 123364787 AGGCAGAGCAGGACGCCGCTGCTGCCGCCGCCACCGCCGCCTCCGCTCCAGTCGCCTCTGGTCCT AGGCAGAGCAGGACGCCGCTGCTGCCGCCGCC___GCCGCCTCCGCTCCAGTCGCCTCTGGTCCT CGGT C MIR8072,SBNO1 Ensembl:ENSG00000284425,Ensembl:ENSG00000139697 miRNA,Protein coding exon,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123364669..123364825 26863196 MeRIP-seq:(Medium) rs539121918 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_230030,Human_RBP_ID_4247115,Human_RBP_ID_8787016,Human_RBP_ID_9279345,Human_RBP_ID_18457105 Human_Splice_Rec_1439573,Human_Splice_Rec_1439635 92562 RMVar_ID_92562 Human_SNP_ID_518907705 m1A Human chr12 - 123364807 123364807 123364807 CAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGACGCCGCTGCTGCCGCCGCCACCGCCGCCTCCG CAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGCCGCCGCTGCTGCCGCCGCCACCGCCGCCTCCG T G MIR8072,SBNO1 Ensembl:ENSG00000284425,Ensembl:ENSG00000139697 miRNA,Protein coding exon,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:123364722..123364887 26863196 MeRIP-seq:(Medium) rs1262473597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230030,Human_RBP_ID_4247115,Human_RBP_ID_8787016,Human_RBP_ID_9279345,Human_RBP_ID_17357423,Human_RBP_ID_18457105 92563 RMVar_ID_92563 Human_SNP_ID_518907708 m1A Human chr12 - 123364810 123364810 123364810 CGTCAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGACGCCGCTGCTGCCGCCGCCACCGCCGCCT CGTCAAGATGGCGGCGGGGAGGTAGGCAGAGCGGGACGCCGCTGCTGCCGCCGCCACCGCCGCCT T C MIR8072,SBNO1 Ensembl:ENSG00000284425,Ensembl:ENSG00000139697 miRNA,Protein coding exon,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123350383..123364827 26863196 MeRIP-seq:(Medium) rs1030822454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230030,Human_RBP_ID_4247115,Human_RBP_ID_8777876,Human_RBP_ID_9279345,Human_RBP_ID_11864974,Human_RBP_ID_17357423,Human_RBP_ID_18457105,Human_RBP_ID_23125236 92564 RMVar_ID_92564 Human_SNP_ID_518907709 m1A Human chr12 - 123364810 123364810 123364810 CGTCAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGACGCCGCTGCTGCCGCCGCCACCGCCGCCT CGTCAAGATGGCGGCGGGGAGGTAGGCAGAGCCGGACGCCGCTGCTGCCGCCGCCACCGCCGCCT T G MIR8072,SBNO1 Ensembl:ENSG00000284425,Ensembl:ENSG00000139697 miRNA,Protein coding exon,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123350383..123364827 26863196 MeRIP-seq:(Medium) rs1030822454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230030,Human_RBP_ID_4247115,Human_RBP_ID_8777876,Human_RBP_ID_9279345,Human_RBP_ID_11864974,Human_RBP_ID_17357423,Human_RBP_ID_18457105,Human_RBP_ID_23125236 92565 RMVar_ID_92565 Human_SNP_ID_518907871 m1A Human chr12 + 123365047 123365047 123365047 TCTTGACCACCCCCCAGTCTTCGCCGCCAAAAACGGACTCCGCCGGCTATCCTCGGCCCGGTACC TCTTGACCACCCCCCAGTCTTCGCCGCCAAAACCGGACTCCGCCGGCTATCCTCGGCCCGGTACC A C SBNO1-AS1 Ensembl:ENSG00000256092 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123364999..123365167 26863196 MeRIP-seq:(Medium) rs1165189405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3421764 Human_Splice_Rec_1439697 92566 RMVar_ID_92566 Human_SNP_ID_518913387 m1A Human chr12 - 123384200 123384200 123384200 GGTGCCGGCCACTTGGGCAAATACCTCTAGCCATGGCTCCACTCTGTCACCGCCTGGGATCTCCC GGTGCCGGCCACTTGGGCAAATACCTCTAGCCGTGGCTCCACTCTGTCACCGCCTGGGATCTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123384151..123388504 26863196 MeRIP-seq:(Medium) rs771910601 Functional Loss SNV dbSNP153 33..33 33 - - - 92567 RMVar_ID_92567 Human_SNP_ID_518916424 m1A Human chr12 - 123395123 123395123 123395123 TCAGATTTTTGGTTTGGAAAAGGTACCAGGGGACCTTTCCTGGCGTCTTTGATCTTCTGTTCCTC TCAGATTTTTGGTTTGGAAAAGGTACCAGGGGCCCTTTCCTGGCGTCTTTGATCTTCTGTTCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123395076..123396400 26863196 MeRIP-seq:(Medium) rs774856187 Functional Loss SNV dbSNP153 33..33 33 - - - 92568 RMVar_ID_92568 Human_SNP_ID_518920320 m1A Human chr12 + 123409119 123409119 123409119 GAGAGGCTGTCCTCGTCTTTGATTCCCCCCCAACCCCACCTCGGGCCTCACGACGGTGCTACCTA GAGAGGCTGTCCTCGTCTTTGATTCCCCCCCACCCCCACCTCGGGCCTCACGACGGTGCTACCTA A C KMT5A Ensembl:ENSG00000183955 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123409071..123409200 26863196 MeRIP-seq:(Medium) rs1303521348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413914,Human_RBP_ID_6148501,Human_RBP_ID_11865316,Human_RBP_ID_17812117,Human_RBP_ID_22900386,Human_RBP_ID_26421881 92569 RMVar_ID_92569 Human_SNP_ID_518920321 m1A Human chr12 + 123409119 123409119 123409119 GAGAGGCTGTCCTCGTCTTTGATTCCCCCCCAACCCCACCTCGGGCCTCACGACGGTGCTACCTA GAGAGGCTGTCCTCGTCTTTGATTCCCCCCCAGCCCCACCTCGGGCCTCACGACGGTGCTACCTA A G KMT5A Ensembl:ENSG00000183955 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123409071..123409200 26863196 MeRIP-seq:(Medium) rs1303521348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413914,Human_RBP_ID_6148501,Human_RBP_ID_11865316,Human_RBP_ID_17812117,Human_RBP_ID_22900386,Human_RBP_ID_26421881 92570 RMVar_ID_92570 Human_SNP_ID_518928117 m1A Human chr12 - 123436444 123436444 123436444 AACCTTTGGGAGACTCCAAGACAGCAGCTCCGAGGTCGGCGGGGGTCTGGGTGGCCATGGAGGAG AACCTTTGGGAGACTCCAAGACAGCAGCTCCGTGGTCGGCGGGGGTCTGGGTGGCCATGGAGGAG T A RILPL2 Ensembl:ENSG00000150977 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:123436303..123436457;chr12:123423097..123436715;chr12:123422998..123436687;chr12:123423095..123436670 26863196 MeRIP-seq:(Medium) rs1478416306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9365801,Human_RBP_ID_17812126 RMVar_hsa_circ_83077,RMVar_hsa_circ_161347 92571 RMVar_ID_92571 Human_SNP_ID_518928173 m1A Human chr12 + 123436625 123436625 123436625 GGCCTGCGCCCCGGCGCACCGTCCCCGCTGCCAGCCACGCTGGAGAGTGCGCTCCAGGATGTGGT GGCCTGCGCCCCGGCGCACCGTCCCCGCTGCCCGCCACGCTGGAGAGTGCGCTCCAGGATGTGGT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:123436517..123436679 26863196 MeRIP-seq:(Medium) rs1371954844 Functional Loss SNV dbSNP153 33..33 33 - - - 92572 RMVar_ID_92572 Human_SNP_ID_518935250 m1A Human chr12 + 123458215 123458215 123458215 GTCTCCGTCGGAAGGGAGCCCAAGCTTTGCAGAGGTGAGTGGAAGCGGCTTGGAAGGAGCGGGCC GTCTCCGTCGGAAGGGAGCCCAAGCTTTGCAGCGGTGAGTGGAAGCGGCTTGGAAGGAGCGGGCC A C SNRNP35 Ensembl:ENSG00000184209 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123458174..123459053 26863196 MeRIP-seq:(Medium) rs917409974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875385,Human_RBP_ID_4248316 Human_Splice_Rec_1439785,Human_Splice_Rec_1439787,Human_Splice_Rec_1439789,Human_Splice_Rec_1439791 92573 RMVar_ID_92573 Human_SNP_ID_518935696 m1A Human chr12 + 123459791 123459791 123459791 CCTGGGTGACAGAGTGAGACTTTGTCTCGAGTAAAAAAAGAGAATGTAAAAATCGAAAGAGATTG CCTGGGTGACAGAGTGAGACTTTGTCTCGAGTGAAAAAAGAGAATGTAAAAATCGAAAGAGATTG A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123459786..123459918 26863196 MeRIP-seq:(Medium) rs187002924 Functional Loss SNV dbSNP153 33..33 33 - - - 92574 RMVar_ID_92574 Human_SNP_ID_518937511 m1A Human chr12 + 123466205 123466205 123466205 GCAAGAAAGAGAGCCGACCAGGGTGTGGCCCGACAATGACTGGGAGAGAGAGAGGGACTTCAGAG GCAAGAAAGAGAGCCGACCAGGGTGTGGCCCGTCAATGACTGGGAGAGAGAGAGGGACTTCAGAG A T SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123466051..123466350 26863196 MeRIP-seq:(Medium) rs772824414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811864,Human_RBP_ID_4209483,Human_RBP_ID_5139969,Human_RBP_ID_17650252,Human_RBP_ID_22492606 RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 92575 RMVar_ID_92575 Human_SNP_ID_518937512 m1A Human chr12 - 123466209 123466209 123466209 TCATCTCTGAAGTCCCTCTCTCTCTCCCAGTCATTGTCGGGCCACACCCTGGTCGGCTCTCTTTC TCATCTCTGAAGTCCCTCTCTCTCTCCCAGTCGTTGTCGGGCCACACCCTGGTCGGCTCTCTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:123465547..123466375;chr12:123465805..123466325 26863196 MeRIP-seq:(Medium) rs760666219 Functional Loss SNV dbSNP153 33..33 33 - - - 92576 RMVar_ID_92576 Human_SNP_ID_518950102 m1A Human chr12 - 123513089 123513089 123513089 ACACACAGACGCCACCACACAGACATACACGCACTCACACTGCACACAGCACACACGCAGACCTC ACACACAGACGCCACCACACAGACATACACGCCCTCACACTGCACACAGCACACACGCAGACCTC T G RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123513087..123513185 26863196 MeRIP-seq:(Medium) rs1457398754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194581,Human_RBP_ID_260160,Human_RBP_ID_2310935,Human_RBP_ID_24530041,Human_RBP_ID_26755700 RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 92577 RMVar_ID_92577 Human_SNP_ID_518955771 m1A Human chr12 - 123533212 123533212 123533212 TGCGCCTGGAGCTGGACCGCCTGCGCCTGGAGAGGATGGACCGCATCGAGAAGGAGCGCAAGCAC TGCGCCTGGAGCTGGACCGCCTGCGCCTGGAGCGGATGGACCGCATCGAGAAGGAGCGCAAGCAC T G RILPL1 Ensembl:ENSG00000188026 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:123533162..123533309 26863196 MeRIP-seq:(Medium) rs762942945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9365803,Human_RBP_ID_18978158,Human_RBP_ID_22910923,Human_RBP_ID_23545016,Human_RBP_ID_26322305 Human_Splice_Rec_1439797,Human_Splice_Rec_1439807 92578 RMVar_ID_92578 Human_SNP_ID_518956030 m1A Human chr12 + 123533758 123533758 123533758 CGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGGAGGGCGCGCGCGTGCGCAGGCCCGCGGCGCCTC CGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGGCGGGCGCGCGCGTGCGCAGGCCCGCGGCGCCTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:123533579..123533926 26863196 MeRIP-seq:(Medium) rs1033162843 Functional Loss SNV dbSNP153 33..33 33 - - - 92579 RMVar_ID_92579 Human_SNP_ID_518956031 m1A Human chr12 + 123533758 123533758 123533758 CGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGGAGGGCGCGCGCGTGCGCAGGCCCGCGGCGCCTC CGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGGGGGGCGCGCGCGTGCGCAGGCCCGCGGCGCCTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:123533579..123533926 26863196 MeRIP-seq:(Medium) rs1033162843 Functional Loss SNV dbSNP153 33..33 33 - - - 92580 RMVar_ID_92580 Human_SNP_ID_518969225 m1A Human chr12 + 123584654 123584654 123584654 GGCCTCAGCCCCACCATGGTGACGCTTGCTGAACTGCTGGTGCTTCTGGCCGCTCTCCTGGCCAC GGCCTCAGCCCCACCATGGTGACGCTTGCTGAGCTGCTGGTGCTTCTGGCCGCTCTCCTGGCCAC A G TMED2 Ensembl:ENSG00000086598 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:123584551..123585574 26863410 MeRIP-seq:(Medium) rs199935307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413954,Human_RBP_ID_876654,Human_RBP_ID_1467070,Human_RBP_ID_1789978,Human_RBP_ID_3397138,Human_RBP_ID_4209579,Human_RBP_ID_5416772,Human_RBP_ID_5491102,Human_RBP_ID_6148664,Human_RBP_ID_8368646,Human_RBP_ID_9012728,Human_RBP_ID_9322823,Human_RBP_ID_11866124,Human_RBP_ID_22040466,Human_RBP_ID_22436741,Human_RBP_ID_23125239,Human_RBP_ID_27211817,Human_RBP_ID_27419807 Human_miRNA_ID_2300900,Human_miRNA_ID_2304161,Human_miRNA_ID_2307429 RMVar_hsa_circ_124313,RMVar_hsa_circ_161352 92581 RMVar_ID_92581 Human_SNP_ID_518969230 m1A Human chr12 - 123584665 123584665 123584665 AGCCCGAGACCGTGGCCAGGAGAGCGGCCAGAAGCACCAGCAGTTCAGCAAGCGTCACCATGGTG AGCCCGAGACCGTGGCCAGGAGAGCGGCCAGAGGCACCAGCAGTTCAGCAAGCGTCACCATGGTG T C TMED2-DT Ensembl:ENSG00000247373 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr12:123584574..123584671;chr12:123584580..123584680 26863410 MeRIP-seq:(Medium) rs754658176 Functional Loss SNV dbSNP153 33..33 33 - - - 92582 RMVar_ID_92582 Human_SNP_ID_518969292 m1A Human chr12 + 123584803 123584803 123584803 CATCTTCGAGGTGGCGGAGGGCGGCTTCCTGGACATCGACGTGGAGGTGCGGGCTAGCTGCCCGC CATCTTCGAGGTGGCGGAGGGCGGCTTCCTGGGCATCGACGTGGAGGTGCGGGCTAGCTGCCCGC A G TMED2 Ensembl:ENSG00000086598 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:123584601..123585574 32194978 MeRIP-seq:(Medium) rs1188523458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228507,Human_RBP_ID_413957,Human_RBP_ID_752633,Human_RBP_ID_809744,Human_RBP_ID_876655,Human_RBP_ID_1789981,Human_RBP_ID_4246404,Human_RBP_ID_6148668,Human_RBP_ID_9322824,Human_RBP_ID_9365804,Human_RBP_ID_11866138,Human_RBP_ID_22492611,Human_RBP_ID_23113417 Human_Splice_Rec_1439837,Human_Splice_Rec_1439843,Human_Splice_Rec_1439849,Human_Splice_Rec_1439855 RMVar_hsa_circ_124313,RMVar_hsa_circ_161352 92583 RMVar_ID_92583 Human_SNP_ID_518969343 m1A Human chr12 + 123584918 123584918 123584918 GGCGCGGGGCCTGTGTGGGGAGTGGGCTTGGAAGTCGCTGTCCGAGTCCTGGAGAAGCCCAGGCC GGCGCGGGGCCTGTGTGGGGAGTGGGCTTGGACGTCGCTGTCCGAGTCCTGGAGAAGCCCAGGCC A C TMED2 Ensembl:ENSG00000086598 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123584915..123585065 26863196 MeRIP-seq:(Medium) rs1029857329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8368649,Human_RBP_ID_22040729 RMVar_hsa_circ_124313,RMVar_hsa_circ_161352 92584 RMVar_ID_92584 Human_SNP_ID_518978343 m1A Human chr12 + 123619627 123619627 123619627 GGAGCAACAAAGAAGAGAGAAAACAGAAAATGAAGGGAGAAGAAAATTCATAAAAAATAAAGCTT GGAGCAACAAAGAAGAGAGAAAACAGAAAATGTAGGGAGAAGAAAATTCATAAAAAATAAAGCTT A T DDX55 Ensembl:ENSG00000111364 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123619576..123620075 26863196 MeRIP-seq:(Medium) rs1320397377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1439917,Human_Splice_Rec_1439967,Human_Splice_Rec_1440023 RMVar_hsa_circ_87842,RMVar_hsa_circ_161362,RMVar_hsa_circ_85741,RMVar_hsa_circ_107907,RMVar_hsa_circ_161372,RMVar_hsa_circ_161374 92585 RMVar_ID_92585 Human_SNP_ID_518979341 m1A Human chr12 - 123622726 123622726 123622726 GGAACCAACCAGATGGCTGTGTGTGCCAAAGCACAGAACAAACCTTTCTATGTGGTTGCAGAAAG GGAACCAACCAGATGGCTGTGTGTGCCAAAGCGCAGAACAAACCTTTCTATGTGGTTGCAGAAAG T C EIF2B1 Ensembl:ENSG00000111361 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:123621498..123625988 32194978 MeRIP-seq:(Medium) rs943314619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414082,Human_RBP_ID_875394,Human_RBP_ID_1790078,Human_RBP_ID_18621115,Human_RBP_ID_25016354,Human_RBP_ID_26322320 Human_Splice_Rec_1440036,Human_Splice_Rec_1440044,Human_Splice_Rec_1440054 RMVar_hsa_circ_30173,RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 92586 RMVar_ID_92586 Human_SNP_ID_518980633 m1A Human chr12 - 123627156 123627156 123627156 TGCCCCTTTGACAAAGCTTTCTCGGTCCACAGACAATATTGACTCACGCCTACTCCAGAGTGGTC TGCCCCTTTGACAAAGCTTTCTCGGTCCACAGGCAATATTGACTCACGCCTACTCCAGAGTGGTC T C EIF2B1 Ensembl:ENSG00000111361 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:123627031..123630071 32194978 MeRIP-seq:(Medium) rs769237783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26806308 Human_Splice_Rec_1440032,Human_Splice_Rec_1440042,Human_Splice_Rec_1440062 RMVar_hsa_circ_38129,RMVar_hsa_circ_115197,RMVar_hsa_circ_161375,RMVar_hsa_circ_306871,RMVar_hsa_circ_324591,RMVar_hsa_circ_348531,RMVar_hsa_circ_297053,RMVar_hsa_circ_105703,RMVar_hsa_circ_161376,RMVar_hsa_circ_161377,RMVar_hsa_circ_161378 92587 RMVar_ID_92587 Human_SNP_ID_518982364 m1A Human chr12 + 123633592 123633592 123633592 CGTCCTCCTGCTGCGGAGCCCCAGGGGACCCGAGCCGCCCGCGCTGTCTCGAACGGGTCCGCCGG CGTCCTCCTGCTGCGGAGCCCCAGGGGACCCGGGCCGCCCGCGCTGTCTCGAACGGGTCCGCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:123632396..123633700;chr12:123633498..123633675;chr12:123632420..123633675;chr12:123633507..123633675 26863196 MeRIP-seq:(Medium) rs1355015535 Functional Loss SNV dbSNP153 33..33 33 - - - 92588 RMVar_ID_92588 Human_SNP_ID_518987630 m1A Human chr12 + 123654127 123654112 123654127 GTGTGTGTATTTTGGATGTGTGTGTATTCTGGATGTGTGTATGTGTGTATATTTTGGATGTGTGT GTGTGTGTATTTTGGATG_______________TGTGTGTATGTGTGTATATTTTGGATGTGTGT GTGTGTGTATTCTGGA G GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123654122..123654207 26863196 MeRIP-seq:(Medium) rs1465958702 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_6149124,Human_RBP_ID_23545263 RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_95852,RMVar_hsa_circ_161389,RMVar_hsa_circ_43282,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 92589 RMVar_ID_92589 Human_SNP_ID_518987679 m1A Human chr12 - 123654299 123654285 123654300 CACACACACAACCAAATACACAGCCCCAAAAAATACACATCCAAAACATACCCCCCAAAATACAC CACACACACAACCAAATACACAGCCCCAAAA_______________CATACCCCCCAAAATACAC GTTTTGGATGTGTATT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123654293..123654623 26863196 MeRIP-seq:(Medium) rs1484380407 Functional Loss DEL dbSNP153 32..46 33 - - - 92590 RMVar_ID_92590 Human_SNP_ID_518987727 m1A Human chr12 + 123654455 123654453 123654455 ATTTTGGGTGTATGTCCGTGTGTGTATTTTGTATATGTGTGTGTTTTGGGTGTATGTGTATTTGG ATTTTGGGTGTATGTCCGTGTGTGTATTTTG__TATGTGTGTGTTTTGGGTGTATGTGTATTTGG GTA G GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123654448..123654643 26863196 MeRIP-seq:(Medium) rs767633565 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23545280 RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_95852,RMVar_hsa_circ_161389,RMVar_hsa_circ_43282,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 92591 RMVar_ID_92591 Human_SNP_ID_518991778 m1A Human chr12 - 123671217 123671217 123671217 GAAGCCCATGCCTTAGACCTCGCGGGCCGGGCACAGCAGAACCGCGCCCTCATTAGAACCCAGGA GAAGCCCATGCCTTAGACCTCGCGGGCCGGGCGCAGCAGAACCGCGCCCTCATTAGAACCCAGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123671169..123671258 26863196 MeRIP-seq:(Medium) rs756826958 Functional Loss SNV dbSNP153 33..33 33 - - - 92592 RMVar_ID_92592 Human_SNP_ID_518991779 m1A Human chr12 - 123671217 123671217 123671217 GAAGCCCATGCCTTAGACCTCGCGGGCCGGGCACAGCAGAACCGCGCCCTCATTAGAACCCAGGA GAAGCCCATGCCTTAGACCTCGCGGGCCGGGCCCAGCAGAACCGCGCCCTCATTAGAACCCAGGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123671169..123671258 26863196 MeRIP-seq:(Medium) rs756826958 Functional Loss SNV dbSNP153 33..33 33 - - - 92593 RMVar_ID_92593 Human_SNP_ID_519061932 m1A Human chr12 - 123936970 123936970 123936970 CTCAGCCACACCTTTTCTGTTTAATCCCATGCATGCCAAACACTTTTCACACCTACCGACCCATT CTCAGCCACACCTTTTCTGTTTAATCCCATGCTTGCCAAACACTTTTCACACCTACCGACCCATT T A CCDC92 Ensembl:ENSG00000119242 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123936919..123937110 26863196 MeRIP-seq:(Medium) rs1013346734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27419870 RMVar_hsa_circ_86596,RMVar_hsa_circ_97032,RMVar_hsa_circ_161492,RMVar_hsa_circ_79108,RMVar_hsa_circ_161493,RMVar_hsa_circ_161491 92594 RMVar_ID_92594 Human_SNP_ID_519061948 m1A Human chr12 - 123937028 123937028 123937028 TGAAGCCCGCCGTGCCCCACCCCGCGCTGTCCATGCACTGTGAGCACCACTGGGAAATCTCAGCC TGAAGCCCGCCGTGCCCCACCCCGCGCTGTCCGTGCACTGTGAGCACCACTGGGAAATCTCAGCC T C CCDC92 Ensembl:ENSG00000119242 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123936986..123937093 26863196 MeRIP-seq:(Medium) rs773368767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414238,Human_RBP_ID_27211913 Human_miRNA_ID_330776,Human_miRNA_ID_347885,Human_miRNA_ID_1072082,Human_miRNA_ID_1996086,Human_miRNA_ID_2078922,Human_miRNA_ID_2081238,Human_miRNA_ID_2091784,Human_miRNA_ID_2228579,Human_miRNA_ID_2286010,Human_miRNA_ID_2289008,Human_miRNA_ID_2504557 RMVar_hsa_circ_86596,RMVar_hsa_circ_97032,RMVar_hsa_circ_161492,RMVar_hsa_circ_79108,RMVar_hsa_circ_161493,RMVar_hsa_circ_161491 92595 RMVar_ID_92595 Human_SNP_ID_519062188 m1A Human chr12 - 123937455 123937455 123937455 CAAGCCAGCGCCCCCCAAAGACAAGCTACCCGAAACGCCTCGCCGCCGCATGAAAAAGAGCCTCT CAAGCCAGCGCCCCCCAAAGACAAGCTACCCGGAACGCCTCGCCGCCGCATGAAAAAGAGCCTCT T C CCDC92 Ensembl:ENSG00000119242 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123937347..123937545 26863196 MeRIP-seq:(Medium) rs1311080176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86596,RMVar_hsa_circ_97032,RMVar_hsa_circ_161492,RMVar_hsa_circ_79108,RMVar_hsa_circ_161493,RMVar_hsa_circ_161491 92596 RMVar_ID_92596 Human_SNP_ID_519064382 m1A Human chr12 - 123946018 123946018 123946018 GGATCTGAGAGCTGCTTTCAAAGCAGGATGCCAGCAAGATCATCATGGACTGGAAATGGATGGCG GGATCTGAGAGCTGCTTTCAAAGCAGGATGCCGGCAAGATCATCATGGACTGGAAATGGATGGCG T C CCDC92 Ensembl:ENSG00000119242 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:123945943..123946043;chr12:123945941..123946442 26863196 MeRIP-seq:(Medium) rs980903859 Functional Loss SNV dbSNP153 33..33 33 - - - 92597 RMVar_ID_92597 Human_SNP_ID_519071283 m1A Human chr12 - 123972621 123972621 123972621 GCCCAGGCAGCCCCGCCCGCCGCGCCCCGCCCAGCCCATGGGCCACGGGCCCCCACCGCCGCCCG GCCCAGGCAGCCCCGCCCGCCGCGCCCCGCCCTGCCCATGGGCCACGGGCCCCCACCGCCGCCCG T A CCDC92 Ensembl:ENSG00000119242 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123972581..123972831 26863196 MeRIP-seq:(Medium) rs1566187892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22710372 Human_Splice_Rec_1441119,Human_Splice_Rec_1441131,Human_Splice_Rec_1441149,Human_Splice_Rec_1441167 92598 RMVar_ID_92598 Human_SNP_ID_519071328 m1A Human chr12 - 123972714 123972714 123972714 CCGCGGCTAGCGCTGGGGTGGGAGCGGGCGAGATGCGCCGGGCGGGCGGTGCCCACTGACCTCCC CCGCGGCTAGCGCTGGGGTGGGAGCGGGCGAGGTGCGCCGGGCGGGCGGTGCCCACTGACCTCCC T C CCDC92 Ensembl:ENSG00000119242 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:123972625..123972716 26863410 MeRIP-seq:(Medium) rs1244523247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4251969 92599 RMVar_ID_92599 Human_SNP_ID_519071355 m1A Human chr12 - 123972788 123972788 123972788 CGCCGCCGCGCCGGCGCCTAGCCCGCCGGGTCAGCGCGGCCAGGCCTCGCCGCCGGCCCCGCTCC CGCCGCCGCGCCGGCGCCTAGCCCGCCGGGTCGGCGCGGCCAGGCCTCGCCGCCGGCCCCGCTCC T C CCDC92 Ensembl:ENSG00000119242 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123972531..123973006 26863196 MeRIP-seq:(Medium) rs1356889187 Functional Loss SNV dbSNP153 33..33 33 - - - 92600 RMVar_ID_92600 Human_SNP_ID_519071372 m1A Human chr12 + 123972802 123972802 123972802 GGCGAGGCCTGGCCGCGCTGACCCGGCGGGCTAGGCGCCGGCGCGGCGGCGGGCCTGTGTCTGCC GGCGAGGCCTGGCCGCGCTGACCCGGCGGGCTCGGCGCCGGCGCGGCGGCGGGCCTGTGTCTGCC A C ZNF664 Ensembl:ENSG00000179195 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123972627..123972959 26863196 MeRIP-seq:(Medium) rs959804028 Functional Loss SNV dbSNP153 33..33 33 - - - 92601 RMVar_ID_92601 Human_SNP_ID_519071644 m1A Human chr12 - 123973291 123973291 123973291 CGCGGGCGCCGCGCACCCACCTCCCTCTCCTCAGGGACACCTCACAGGTGCGCCTCCGAGCCGCG CGCGGGCGCCGCGCACCCACCTCCCTCTCCTCGGGGACACCTCACAGGTGCGCCTCCGAGCCGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123973240..123974076 26863196 MeRIP-seq:(Medium) rs1382429233 Functional Loss SNV dbSNP153 33..33 33 - - - 92602 RMVar_ID_92602 Human_SNP_ID_519071645 m1A Human chr12 + 123973296 123973294 123973296 CTCGGAGGCGCACCTGTGAGGTGTCCCTGAGGAGAGGGAGGTGGGTGCGCGGCGCCCGCGGCCTG CTCGGAGGCGCACCTGTGAGGTGTCCCTGAG__GAGGGAGGTGGGTGCGCGGCGCCCGCGGCCTG GGA G RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA 5'UTR,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123973180..123973393 26863196 MeRIP-seq:(Medium) rs896084432 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_229339,Human_RBP_ID_414244,Human_RBP_ID_810817,Human_RBP_ID_4246408,Human_RBP_ID_5314704,Human_RBP_ID_9279348,Human_RBP_ID_9322826,Human_RBP_ID_17357438,Human_RBP_ID_18417683 Human_Splice_Rec_1441191,Human_Splice_Rec_1441199,Human_Splice_Rec_1441205,Human_Splice_Rec_1441213,Human_Splice_Rec_1441221,Human_Splice_Rec_1441223,Human_Splice_Rec_1441225,Human_Splice_Rec_1441235,Human_Splice_Rec_1441241,Human_Splice_Rec_1441259,Human_Splice_Rec_1441265,Human_Splice_Rec_1441273 RMVar_hsa_circ_104122,RMVar_hsa_circ_161495 92603 RMVar_ID_92603 Human_SNP_ID_519071647 m1A Human chr12 + 123973296 123973296 123973296 CTCGGAGGCGCACCTGTGAGGTGTCCCTGAGGAGAGGGAGGTGGGTGCGCGGCGCCCGCGGCCTG CTCGGAGGCGCACCTGTGAGGTGTCCCTGAGGCGAGGGAGGTGGGTGCGCGGCGCCCGCGGCCTG A C RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA 5'UTR,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:123973180..123973393 26863196 MeRIP-seq:(Medium) rs1436773574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229339,Human_RBP_ID_414244,Human_RBP_ID_810817,Human_RBP_ID_4246408,Human_RBP_ID_5314704,Human_RBP_ID_9279348,Human_RBP_ID_9322826,Human_RBP_ID_17357438,Human_RBP_ID_18417683 Human_Splice_Rec_1441191,Human_Splice_Rec_1441199,Human_Splice_Rec_1441205,Human_Splice_Rec_1441213,Human_Splice_Rec_1441221,Human_Splice_Rec_1441223,Human_Splice_Rec_1441225,Human_Splice_Rec_1441235,Human_Splice_Rec_1441241,Human_Splice_Rec_1441259,Human_Splice_Rec_1441265,Human_Splice_Rec_1441273 RMVar_hsa_circ_104122,RMVar_hsa_circ_161495 92604 RMVar_ID_92604 Human_SNP_ID_519071653 m1A Human chr12 + 123973302 123973302 123973302 GGCGCACCTGTGAGGTGTCCCTGAGGAGAGGGAGGTGGGTGCGCGGCGCCCGCGGCCTGGGGCGC GGCGCACCTGTGAGGTGTCCCTGAGGAGAGGGGGGTGGGTGCGCGGCGCCCGCGGCCTGGGGCGC A G RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA 5'UTR,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123973147..123973394 26863196 MeRIP-seq:(Medium) rs1280065560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229339,Human_RBP_ID_414244,Human_RBP_ID_753462,Human_RBP_ID_810817,Human_RBP_ID_4246408,Human_RBP_ID_5314704,Human_RBP_ID_9279348,Human_RBP_ID_9322826,Human_RBP_ID_17357438,Human_RBP_ID_18417683 Human_Splice_Rec_1441191,Human_Splice_Rec_1441199,Human_Splice_Rec_1441205,Human_Splice_Rec_1441213,Human_Splice_Rec_1441221,Human_Splice_Rec_1441223,Human_Splice_Rec_1441225,Human_Splice_Rec_1441235,Human_Splice_Rec_1441241,Human_Splice_Rec_1441259,Human_Splice_Rec_1441265,Human_Splice_Rec_1441273 RMVar_hsa_circ_104122,RMVar_hsa_circ_161495 92605 RMVar_ID_92605 Human_SNP_ID_519071678 m1A Human chr12 + 123973352 123973352 123973352 CGCGGCCTGGGGCGCTGACTCCCCTCACTTGGAGTGAGTTCTCGGCGGCCGGGCTGCAGTCTTTC CGCGGCCTGGGGCGCTGACTCCCCTCACTTGGTGTGAGTTCTCGGCGGCCGGGCTGCAGTCTTTC A T RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA 5'UTR,intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:123973285..123973385 32194978 MeRIP-seq:(Medium) rs1010089264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246408,Human_RBP_ID_17357438,Human_RBP_ID_18206254 Human_Splice_Rec_1441199,Human_Splice_Rec_1441205,Human_Splice_Rec_1441213,Human_Splice_Rec_1441221,Human_Splice_Rec_1441259,Human_Splice_Rec_1441265 RMVar_hsa_circ_104122,RMVar_hsa_circ_161495 92606 RMVar_ID_92606 Human_SNP_ID_519074589 m1A Human chr12 + 123984283 123984283 123984283 ACACAGAGGCCGTAGGGTCACAGAAGGAGCCAAGGGAGTGTGGCCAGTAATGTCCAGTGGGATAA ACACAGAGGCCGTAGGGTCACAGAAGGAGCCACGGGAGTGTGGCCAGTAATGTCCAGTGGGATAA A C RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:123984279..123984538 26863196 MeRIP-seq:(Medium) rs958110838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9669630 RMVar_hsa_circ_12289,RMVar_hsa_circ_104122,RMVar_hsa_circ_161495 92607 RMVar_ID_92607 Human_SNP_ID_519078738 m1A Human chr12 - 124002329 124002329 124002329 TCACTGGCTCACAAGCTGGAGGTGGCCCAGCCACCGCCTCCTTCCAACCTCACCTCCTGCACTCT TCACTGGCTCACAAGCTGGAGGTGGCCCAGCCGCCGCCTCCTTCCAACCTCACCTCCTGCACTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124002323..124002776 26863196 MeRIP-seq:(Medium) rs1686730 Functional Loss SNV dbSNP153 33..33 33 - - - 92608 RMVar_ID_92608 Human_SNP_ID_519081266 m1A Human chr12 + 124012697 124012697 124012697 ATGAGTGTGGGAAGGCGTTCAGTCAGAGTTCGAGCCTCTGCATCCACCAGAGAGTCCACACTGGA ATGAGTGTGGGAAGGCGTTCAGTCAGAGTTCGTGCCTCTGCATCCACCAGAGAGTCCACACTGGA A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs760212002 Functional Loss SNV dbSNP153 33..33 33 - - - 92609 RMVar_ID_92609 Human_SNP_ID_519081454 m1A Human chr12 + 124013225 124013225 124013225 GCCTCCATAGTTGAAAGACTACACAAAAAGCCACAATCATTGCCCGGCCTCCTGAGTCACCTTCT GCCTCCATAGTTGAAAGACTACACAAAAAGCCGCAATCATTGCCCGGCCTCCTGAGTCACCTTCT A G RFLNA,ZNF664,AC068790.8 Ensembl:ENSG00000178882,Ensembl:ENSG00000179195,Ensembl:ENSG00000274874 Protein coding,Protein coding,lincRNA intron,3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124013175..124013332 26863196 MeRIP-seq:(Medium) rs1025639437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414312,Human_RBP_ID_1467336,Human_RBP_ID_3397414,Human_RBP_ID_6149750,Human_RBP_ID_9012847,Human_RBP_ID_9712029,Human_RBP_ID_17236868,Human_RBP_ID_17352552,Human_RBP_ID_17469049,Human_RBP_ID_27419900 Human_miRNA_ID_629411,Human_miRNA_ID_1502418 92610 RMVar_ID_92610 Human_SNP_ID_519081723 m1A Human chr12 - 124014061 124014061 124014061 ATCATCTGTCTCCTCCACCAGAAGTAAACTCCACAAGAGTAGGGACCTTGTCTGTCTCATCAGTG ATCATCTGTCTCCTCCACCAGAAGTAAACTCCGCAAGAGTAGGGACCTTGTCTGTCTCATCAGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124014011..124014150 26863196 MeRIP-seq:(Medium) rs1033079761 Functional Loss SNV dbSNP153 33..33 33 - - - 92611 RMVar_ID_92611 Human_SNP_ID_519158964 m1A Human chr12 - 124324515 124324515 124324515 CGCTGTGTCCTCCCTCCCTCCCTTCCTTGGGCAGAATGAATTCGATGCGTATTCTGTGGCCGCCA CGCTGTGTCCTCCCTCCCTCCCTTCCTTGGGCGGAATGAATTCGATGCGTATTCTGTGGCCGCCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124324464..124324650 32194978 MeRIP-seq:(Medium) rs936298864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37165,Human_RBP_ID_5235750,Human_RBP_ID_18188968,Human_RBP_ID_27419915 Human_miRNA_ID_926639 92612 RMVar_ID_92612 Human_SNP_ID_519158965 m1A Human chr12 - 124324515 124324515 124324515 CGCTGTGTCCTCCCTCCCTCCCTTCCTTGGGCAGAATGAATTCGATGCGTATTCTGTGGCCGCCA CGCTGTGTCCTCCCTCCCTCCCTTCCTTGGGCCGAATGAATTCGATGCGTATTCTGTGGCCGCCA T G NCOR2 Ensembl:ENSG00000196498 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124324464..124324650 32194978 MeRIP-seq:(Medium) rs936298864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37165,Human_RBP_ID_5235750,Human_RBP_ID_18188968,Human_RBP_ID_27419915 Human_miRNA_ID_926639 92613 RMVar_ID_92613 Human_SNP_ID_519158998 m1A Human chr12 + 124324590 124324590 124324590 CAGCAGTCCCCGCCCCCTTGGTCCTGCGAGTGATGGGGTCACCGACTGTCGGCCTGCACACGCCT CAGCAGTCCCCGCCCCCTTGGTCCTGCGAGTGGTGGGGTCACCGACTGTCGGCCTGCACACGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124324540..124324657 26863196 MeRIP-seq:(Medium) rs1362839063 Functional Loss SNV dbSNP153 33..33 33 - - - 92614 RMVar_ID_92614 Human_SNP_ID_519159119 m1A Human chr12 - 124324944 124324938 124324944 CATCCCGCTTAGCGCTCTGGACAGATGGACGCAGGCCCTGTCCAGCCCCCAGTGCGCTCGTTCCG CATCCCGCTTAGCGCTCTGGACAGATGGACGC______TGTCCAGCCCCCAGTGCGCTCGTTCCG AGGGCCT A NCOR2 Ensembl:ENSG00000196498 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124324681..124325161 26863196 MeRIP-seq:(Medium) rs1194141189 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4210286,Human_RBP_ID_17357439,Human_RBP_ID_26421894 92615 RMVar_ID_92615 Human_SNP_ID_519159147 m1A Human chr12 - 124325002 124325002 124325002 GCATTTGGAACCAAAGTCTAAACTGAGCTCGCAGCCCCCGCGCCCTCCCTCCGCCTCCCATCCCG GCATTTGGAACCAAAGTCTAAACTGAGCTCGCGGCCCCCGCGCCCTCCCTCCGCCTCCCATCCCG T C NCOR2 Ensembl:ENSG00000196498 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124324751..124325050 26863196 MeRIP-seq:(Medium) rs889543069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8247540,Human_RBP_ID_8368916,Human_RBP_ID_17357439,Human_RBP_ID_18188970,Human_RBP_ID_26421894,Human_RBP_ID_27419921 92616 RMVar_ID_92616 Human_SNP_ID_519159519 m1A Human chr12 - 124325563 124325563 124325563 TTCTTCCCGCAGGTTCCACGCCATTCCCCTACAACCCCCTGATCATGCGGCTGCAGGCGGGTGTC TTCTTCCCGCAGGTTCCACGCCATTCCCCTACGACCCCCTGATCATGCGGCTGCAGGCGGGTGTC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124325462..124325563 26863410 MeRIP-seq:(Medium) rs995765280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17236905,Human_RBP_ID_17812469 Human_Splice_Rec_1441382,Human_Splice_Rec_1441474,Human_Splice_Rec_1441542,Human_Splice_Rec_1441612,Human_Splice_Rec_1441704,Human_Splice_Rec_1441712,Human_Splice_Rec_1441722,Human_Splice_Rec_1441726 92617 RMVar_ID_92617 Human_SNP_ID_519159733 m1A Human chr12 - 124326256 124326256 124326256 CCGGCCACCCTCTGTCTCCTCAGTGCACTCGGAGGGAGACTGCAACCGCCGGACGCCGCTCACCA CCGGCCACCCTCTGTCTCCTCAGTGCACTCGGGGGGAGACTGCAACCGCCGGACGCCGCTCACCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124326251..124327439 26863410 MeRIP-seq:(Medium) rs771099650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17650027 Human_Splice_Rec_1441381,Human_Splice_Rec_1441473,Human_Splice_Rec_1441541,Human_Splice_Rec_1441611,Human_Splice_Rec_1441703,Human_Splice_Rec_1441711,Human_Splice_Rec_1441721,Human_Splice_Rec_1441725 92618 RMVar_ID_92618 Human_SNP_ID_519162785 m1A Human chr12 - 124334619 124334619 124334619 CTGCCTGACTCTGGGCCCCCCCACTTGCCTGCAGGAGGTCATCACACAGGACTACACCCGGCACC CTGCCTGACTCTGGGCCCCCCCACTTGCCTGCGGGAGGTCATCACACAGGACTACACCCGGCACC T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124334509..124334652 26863196 MeRIP-seq:(Medium) rs112688899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322829,Human_RBP_ID_22538991,Human_RBP_ID_22647084 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161512 92619 RMVar_ID_92619 Human_SNP_ID_519162948 m1A Human chr12 - 124335128 124335128 124335128 TGGTCACCCTGGCCCAGCACATCAGTGTAACTACGCGTTCTCTGCTGCTGCTTGTCACCTTTGCA TGGTCACCCTGGCCCAGCACATCAGTGTAACTGCGCGTTCTCTGCTGCTGCTTGTCACCTTTGCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124335126..124335300 26863196 MeRIP-seq:(Medium) rs1162862210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059726 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161512 92620 RMVar_ID_92620 Human_SNP_ID_519163228 m1A Human chr12 - 124335836 124335836 124335836 CCCTCTCTGTCTGTCTCTGTCCCGGGCTCTGCATCTCTCTCCACCTCTCCCTTGGCCTCCCTGTC CCCTCTCTGTCTGTCTCTGTCCCGGGCTCTGCGTCTCTCTCCACCTCTCCCTTGGCCTCCCTGTC T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124335834..124335949 26863196 MeRIP-seq:(Medium) rs1010818589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17075398,Human_RBP_ID_18934845,Human_RBP_ID_19701944,Human_RBP_ID_24946744 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92621 RMVar_ID_92621 Human_SNP_ID_519163577 m1A Human chr12 - 124336835 124336835 124336835 CCTCACCACGCCAGCCCGGACCCGCCGGCGCCACCTGCCTCGGCCTCGGACCCGCACCGGGAAAA CCTCACCACGCCAGCCCGGACCCGCCGGCGCCTCCTGCCTCGGCCTCGGACCCGCACCGGGAAAA T A NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124336776..124336931 26863196 MeRIP-seq:(Medium) rs759160238 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4210325,Human_RBP_ID_8787023,Human_RBP_ID_9279353,Human_RBP_ID_17357798,Human_RBP_ID_26323639 Human_Splice_Rec_1441365,Human_Splice_Rec_1441457,Human_Splice_Rec_1441525,Human_Splice_Rec_1441595,Human_Splice_Rec_1441687 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161514,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92622 RMVar_ID_92622 Human_SNP_ID_519163578 m1A Human chr12 - 124336835 124336835 124336835 CCTCACCACGCCAGCCCGGACCCGCCGGCGCCACCTGCCTCGGCCTCGGACCCGCACCGGGAAAA CCTCACCACGCCAGCCCGGACCCGCCGGCGCCGCCTGCCTCGGCCTCGGACCCGCACCGGGAAAA T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124336776..124336931 26863196 MeRIP-seq:(Medium) rs759160238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210325,Human_RBP_ID_8787023,Human_RBP_ID_9279353,Human_RBP_ID_17357798,Human_RBP_ID_26323639 Human_Splice_Rec_1441365,Human_Splice_Rec_1441457,Human_Splice_Rec_1441525,Human_Splice_Rec_1441595,Human_Splice_Rec_1441687 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161514,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92623 RMVar_ID_92623 Human_SNP_ID_519163592 m1A Human chr12 - 124336848 124336848 124336848 GAAGAACCTCGCACCTCACCACGCCAGCCCGGACCCGCCGGCGCCACCTGCCTCGGCCTCGGACC GAAGAACCTCGCACCTCACCACGCCAGCCCGGCCCCGCCGGCGCCACCTGCCTCGGCCTCGGACC T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:124336760..124337100 26863196 MeRIP-seq:(Medium) rs1024549976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8787023,Human_RBP_ID_9279353,Human_RBP_ID_17357798 Human_Splice_Rec_1441365,Human_Splice_Rec_1441457,Human_Splice_Rec_1441525,Human_Splice_Rec_1441595,Human_Splice_Rec_1441687 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161514,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92624 RMVar_ID_92624 Human_SNP_ID_519163602 m1A Human chr12 - 124336863 124336863 124336863 CGCCCGCACCCCTGCGAAGAACCTCGCACCTCACCACGCCAGCCCGGACCCGCCGGCGCCACCTG CGCCCGCACCCCTGCGAAGAACCTCGCACCTCCCCACGCCAGCCCGGACCCGCCGGCGCCACCTG T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:124336715..124337207;chr12:124336731..124337200;chr12:124336776..124337068 26863196 MeRIP-seq:(Medium) rs533590387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35919,Human_RBP_ID_9279353,Human_RBP_ID_17357798,Human_RBP_ID_18188978 Human_miRNA_ID_2007252 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161514,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92625 RMVar_ID_92625 Human_SNP_ID_519163770 m1A Human chr12 - 124337176 124337176 124337176 TGCCTGACCGCCTTCTCTCCTCCCCCAGGTCCACCTCCACCTCCTCACCCGTTCGCCCGGCTGCC TGCCTGACCGCCTTCTCTCCTCCCCCAGGTCCTCCTCCACCTCCTCACCCGTTCGCCCGGCTGCC T A NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124337126..124337175 26863196 MeRIP-seq:(Medium) rs373637496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210333,Human_RBP_ID_17357441,Human_RBP_ID_17474880,Human_RBP_ID_18935792 Human_Splice_Rec_1441364,Human_Splice_Rec_1441456,Human_Splice_Rec_1441524,Human_Splice_Rec_1441594,Human_Splice_Rec_1441686,Human_Splice_Rec_1441748 Human_miRNA_ID_98451 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 92626 RMVar_ID_92626 Human_SNP_ID_519164876 m1A Human chr12 + 124340170 124340170 124340170 GAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCACCCCCGCCGCTGCTGCCGCTGCTCTGCTCTGT GAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCCCCCCCGCCGCTGCTGCCGCTGCTCTGCTCTGT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124340078..124340179 26863410 MeRIP-seq:(Medium) rs80209266 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 92627 RMVar_ID_92627 Human_SNP_ID_519164877 m1A Human chr12 + 124340170 124340170 124340170 GAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCACCCCCGCCGCTGCTGCCGCTGCTCTGCTCTGT GAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCGCCCCCGCCGCTGCTGCCGCTGCTCTGCTCTGT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124340078..124340179 26863410 MeRIP-seq:(Medium) rs80209266 Functional Loss SNV dbSNP153 33..33 33 - - - 92628 RMVar_ID_92628 Human_SNP_ID_519165018 m1A Human chr12 - 124340376 124340358 124340376 TCCTCGTCCGAGCGGGAGCGAGACCGGGATCGAGAGCGGGACCGGGATCGGGAGCGGGAAAAGTC TCCTCGTCCGAGCGGGAGCGAGACCGGGATCG__________________GGAGCGGGAAAAGTC CCGATCCCGGTCCCGCTCT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124340259..124340376 26863196 MeRIP-seq:(Medium) rs1271707581 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_8787024,Human_RBP_ID_9279930,Human_RBP_ID_18188981 Human_Splice_Rec_1441360,Human_Splice_Rec_1441361,Human_Splice_Rec_1441452,Human_Splice_Rec_1441453,Human_Splice_Rec_1441520,Human_Splice_Rec_1441521,Human_Splice_Rec_1441590,Human_Splice_Rec_1441591,Human_Splice_Rec_1441682,Human_Splice_Rec_1441683,Human_Splice_Rec_1441744,Human_Splice_Rec_1441745,Human_Splice_Rec_1441752,Human_Splice_Rec_1441753 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92629 RMVar_ID_92629 Human_SNP_ID_519165035 m1A Human chr12 - 124340376 124340376 124340376 TCCTCGTCCGAGCGGGAGCGAGACCGGGATCGAGAGCGGGACCGGGATCGGGAGCGGGAAAAGTC TCCTCGTCCGAGCGGGAGCGAGACCGGGATCGGGAGCGGGACCGGGATCGGGAGCGGGAAAAGTC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124340259..124340376 26863196 MeRIP-seq:(Medium) rs1193843649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8787024,Human_RBP_ID_9279930,Human_RBP_ID_18188981 Human_Splice_Rec_1441360,Human_Splice_Rec_1441361,Human_Splice_Rec_1441452,Human_Splice_Rec_1441453,Human_Splice_Rec_1441520,Human_Splice_Rec_1441521,Human_Splice_Rec_1441590,Human_Splice_Rec_1441591,Human_Splice_Rec_1441682,Human_Splice_Rec_1441683,Human_Splice_Rec_1441744,Human_Splice_Rec_1441745,Human_Splice_Rec_1441752,Human_Splice_Rec_1441753 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92630 RMVar_ID_92630 Human_SNP_ID_519165170 m1A Human chr12 - 124340653 124340653 124340653 CCACCGCCATGGACCGCCTTGCCTACCTCCCCACCGCGCCCCAGCCCTTCAGCAGCCGCCACAGC CCACCGCCATGGACCGCCTTGCCTACCTCCCCCCCGCGCCCCAGCCCTTCAGCAGCCGCCACAGC T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124340460..124340775 26863196 MeRIP-seq:(Medium) rs780703898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357802,Human_RBP_ID_17475100,Human_RBP_ID_18189266 Human_Splice_Rec_1441358,Human_Splice_Rec_1441359,Human_Splice_Rec_1441450,Human_Splice_Rec_1441451,Human_Splice_Rec_1441518,Human_Splice_Rec_1441519,Human_Splice_Rec_1441588,Human_Splice_Rec_1441589,Human_Splice_Rec_1441680,Human_Splice_Rec_1441681,Human_Splice_Rec_1441750,Human_Splice_Rec_1441751 Human_miRNA_ID_1356242,Human_miRNA_ID_2367492,Human_miRNA_ID_2685034,Human_miRNA_ID_2725993,Human_miRNA_ID_3015286 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92631 RMVar_ID_92631 Human_SNP_ID_519165174 m1A Human chr12 + 124340658 124340658 124340658 GGCGGCTGCTGAAGGGCTGGGGCGCGGTGGGGAGGTAGGCAAGGCGGTCCATGGCGGTGGCTGGG GGCGGCTGCTGAAGGGCTGGGGCGCGGTGGGGGGGTAGGCAAGGCGGTCCATGGCGGTGGCTGGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124340601..124340801 26863196 MeRIP-seq:(Medium) rs900561965 Functional Loss SNV dbSNP153 33..33 33 - - - 92632 RMVar_ID_92632 Human_SNP_ID_519165200 m1A Human chr12 + 124340709 124340709 124340709 TGGCGGTGGCTGGGGTGCCTGGTGTCGGGGGCACGAGCACAGGCAGGTGTGGCACTTGGGACAGG TGGCGGTGGCTGGGGTGCCTGGTGTCGGGGGCGCGAGCACAGGCAGGTGTGGCACTTGGGACAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124340587..124340750 26863196 MeRIP-seq:(Medium) rs565085130 Functional Loss SNV dbSNP153 33..33 33 - - - 92633 RMVar_ID_92633 Human_SNP_ID_519165204 m1A Human chr12 - 124340724 124340724 124340724 CGCAGGCATCATCGACCTGTCCCAAGTGCCACACCTGCCTGTGCTCGTGCCCCCGACACCAGGCA CGCAGGCATCATCGACCTGTCCCAAGTGCCACGCCTGCCTGTGCTCGTGCCCCCGACACCAGGCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124340625..124343200 26863410 MeRIP-seq:(Medium) rs532473630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210342,Human_RBP_ID_8368933,Human_RBP_ID_18188982 Human_Splice_Rec_1441358,Human_Splice_Rec_1441450,Human_Splice_Rec_1441518,Human_Splice_Rec_1441588,Human_Splice_Rec_1441680 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92634 RMVar_ID_92634 Human_SNP_ID_519165205 m1A Human chr12 - 124340724 124340724 124340724 CGCAGGCATCATCGACCTGTCCCAAGTGCCACACCTGCCTGTGCTCGTGCCCCCGACACCAGGCA CGCAGGCATCATCGACCTGTCCCAAGTGCCACCCCTGCCTGTGCTCGTGCCCCCGACACCAGGCA T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124340625..124343200 26863410 MeRIP-seq:(Medium) rs532473630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210342,Human_RBP_ID_8368933,Human_RBP_ID_18188982 Human_Splice_Rec_1441358,Human_Splice_Rec_1441450,Human_Splice_Rec_1441518,Human_Splice_Rec_1441588,Human_Splice_Rec_1441680 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92635 RMVar_ID_92635 Human_SNP_ID_519165210 m1A Human chr12 - 124340742 124340742 124340742 CCCTGGCCCAACACCTCCCGCAGGCATCATCGACCTGTCCCAAGTGCCACACCTGCCTGTGCTCG CCCTGGCCCAACACCTCCCGCAGGCATCATCGGCCTGTCCCAAGTGCCACACCTGCCTGTGCTCG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124340568..124340780 26863196 MeRIP-seq:(Medium) rs1371175273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18188982 Human_Splice_Rec_1441358,Human_Splice_Rec_1441450,Human_Splice_Rec_1441518,Human_Splice_Rec_1441588,Human_Splice_Rec_1441680 Human_miRNA_ID_2479242 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 92636 RMVar_ID_92636 Human_SNP_ID_519165597 m1A Human chr12 + 124342002 124342002 124342002 TCTCCAGCGCCGCCGTGTCGGGGTAGCCGCGGATGAGGTAGGGTGGGTACAGGTGCGGGTAGGTG TCTCCAGCGCCGCCGTGTCGGGGTAGCCGCGGGTGAGGTAGGGTGGGTACAGGTGCGGGTAGGTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124341951..124342170 26863196 MeRIP-seq:(Medium) rs1247399574 Functional Loss SNV dbSNP153 33..33 33 - - - 92637 RMVar_ID_92637 Human_SNP_ID_519167146 m1A Human chr12 - 124346572 124346572 124346572 CCCTGGCCCCGCGGCCGCTCAAGGAGGGCTCCATCACGCAGGTATGGCCCAGGGCCAGGCACACG CCCTGGCCCCGCGGCCGCTCAAGGAGGGCTCCGTCACGCAGGTATGGCCCAGGGCCAGGCACACG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124346551..124346575 26863196 MeRIP-seq:(Medium) rs768456898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059729 Human_Splice_Rec_1441351,Human_Splice_Rec_1441443,Human_Splice_Rec_1441511,Human_Splice_Rec_1441581,Human_Splice_Rec_1441673 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_40459,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_67558 92638 RMVar_ID_92638 Human_SNP_ID_519167231 m1A Human chr12 - 124346743 124346743 124346743 CGCCTCCGCCCCCACCGCCCTCACGGGACCTGACCGAGGCCTACAAGACGCAGGCCCTGGGCCCC CGCCTCCGCCCCCACCGCCCTCACGGGACCTGGCCGAGGCCTACAAGACGCAGGCCCTGGGCCCC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124343025..124347407 32194978 MeRIP-seq:(Medium) rs1463955435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_40459,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_67558 92639 RMVar_ID_92639 Human_SNP_ID_519167777 m1A Human chr12 - 124348236 124348236 124348236 CTCAGGACCCCCCCATGAGACGGCCGCCCCCAAGCGCACCTATGACATGATGGAGGGCCGCGTGG CTCAGGACCCCCCCATGAGACGGCCGCCCCCAGGCGCACCTATGACATGATGGAGGGCCGCGTGG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124348144..124348307 26863196 MeRIP-seq:(Medium) rs772869612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8787029,Human_RBP_ID_9279933 Human_Splice_Rec_1441346,Human_Splice_Rec_1441347,Human_Splice_Rec_1441438,Human_Splice_Rec_1441439,Human_Splice_Rec_1441506,Human_Splice_Rec_1441507,Human_Splice_Rec_1441576,Human_Splice_Rec_1441577,Human_Splice_Rec_1441668,Human_Splice_Rec_1441669,Human_Splice_Rec_1441814,Human_Splice_Rec_1441815,Human_Splice_Rec_1441819 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_40459,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_50097,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_67558,RMVar_hsa_circ_326236,RMVar_hsa_circ_346115,RMVar_hsa_circ_282681,RMVar_hsa_circ_53149,RMVar_hsa_circ_161517 92640 RMVar_ID_92640 Human_SNP_ID_519170417 m1A Human chr12 - 124356692 124356692 124356692 GCCCTTCCCCGTGCCCCCCCGTGAGGTGATCAAGGCCTCCCCGCATGCCCCGGACCCCTCAGCCT GCCCTTCCCCGTGCCCCCCCGTGAGGTGATCACGGCCTCCCCGCATGCCCCGGACCCCTCAGCCT T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:124356608..124356838;chr12:124356602..124356869 26863196 MeRIP-seq:(Medium) rs1369108347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35937,Human_RBP_ID_5127244,Human_RBP_ID_9279934 Human_Splice_Rec_1441334,Human_Splice_Rec_1441335,Human_Splice_Rec_1441427,Human_Splice_Rec_1441495,Human_Splice_Rec_1441565,Human_Splice_Rec_1441657,Human_Splice_Rec_1441803,Human_Splice_Rec_1441821,Human_Splice_Rec_1441825 Human_miRNA_ID_1966174,Human_miRNA_ID_1966175,Human_miRNA_ID_2361631,Human_miRNA_ID_2361632 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_50097,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_346115,RMVar_hsa_circ_104619,RMVar_hsa_circ_25865,RMVar_hsa_circ_161518 92641 RMVar_ID_92641 Human_SNP_ID_519170419 m1A Human chr12 - 124356696 124356696 124356696 GCCTGCCCTTCCCCGTGCCCCCCCGTGAGGTGATCAAGGCCTCCCCGCATGCCCCGGACCCCTCA GCCTGCCCTTCCCCGTGCCCCCCCGTGAGGTGGTCAAGGCCTCCCCGCATGCCCCGGACCCCTCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr12:124355426..124356808;chr12:124356626..124356725 26863196 MeRIP-seq:(Medium) rs767718046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35937,Human_RBP_ID_5127244,Human_RBP_ID_9279934 Human_Splice_Rec_1441334,Human_Splice_Rec_1441335,Human_Splice_Rec_1441427,Human_Splice_Rec_1441495,Human_Splice_Rec_1441565,Human_Splice_Rec_1441657,Human_Splice_Rec_1441803,Human_Splice_Rec_1441821,Human_Splice_Rec_1441825 Human_miRNA_ID_1966174,Human_miRNA_ID_1966175,Human_miRNA_ID_2361631,Human_miRNA_ID_2361632 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_50097,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_346115,RMVar_hsa_circ_104619,RMVar_hsa_circ_25865,RMVar_hsa_circ_161518 92642 RMVar_ID_92642 Human_SNP_ID_519170420 m1A Human chr12 + 124356698 124356698 124356698 AGGGGTCCGGGGCATGCGGGGAGGCCTTGATCACCTCACGGGGGGGCACGGGGAAGGGCAGGCCG AGGGGTCCGGGGCATGCGGGGAGGCCTTGATCCCCTCACGGGGGGGCACGGGGAAGGGCAGGCCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124356626..124356700 26863196 MeRIP-seq:(Medium) rs1376129058 Functional Loss SNV dbSNP153 33..33 33 - - - 92643 RMVar_ID_92643 Human_SNP_ID_519170437 m1A Human chr12 + 124356720 124356720 124356720 GGCCTTGATCACCTCACGGGGGGGCACGGGGAAGGGCAGGCCGGAAGTCCAGCAAGGGGGGTCCC GGCCTTGATCACCTCACGGGGGGGCACGGGGAGGGGCAGGCCGGAAGTCCAGCAAGGGGGGTCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:124356557..124356846 26863196 MeRIP-seq:(Medium) rs745530821 Functional Loss SNV dbSNP153 33..33 33 - - - 92644 RMVar_ID_92644 Human_SNP_ID_519170476 m1A Human chr12 - 124356801 124356801 124356801 TCTGACTGCCCCACCTCCTGCCCTCAGCAGAGAAGCCTGTGTTCTTCCCAGCCTTCGCAGCCGAG TCTGACTGCCCCACCTCCTGCCCTCAGCAGAGGAGCCTGTGTTCTTCCCAGCCTTCGCAGCCGAG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124356751..124356800 26863196 MeRIP-seq:(Medium) rs889545982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1441426,Human_Splice_Rec_1441494,Human_Splice_Rec_1441564,Human_Splice_Rec_1441656,Human_Splice_Rec_1441802 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_346115,RMVar_hsa_circ_104619,RMVar_hsa_circ_25865,RMVar_hsa_circ_161518 92645 RMVar_ID_92645 Human_SNP_ID_519172570 m1A Human chr12 + 124362284 124362284 124362284 TGGGAGCTGCGTCCTCCCGGGGGGGCTCATGGACTTTGGTGACCTGCTGAGGGAAGCAGGCAGAA TGGGAGCTGCGTCCTCCCGGGGGGGCTCATGGGCTTTGGTGACCTGCTGAGGGAAGCAGGCAGAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124361993..124362337 26863196 MeRIP-seq:(Medium) rs1182951497 Functional Loss SNV dbSNP153 33..33 33 - - - 92646 RMVar_ID_92646 Human_SNP_ID_519173033 m1A Human chr12 - 124363786 124363786 124363786 GGTGCTCGTGTGCCCGCAGGCTGCTGTCCCCAAGGCCCAGCCTCCTCACCCCGACTGGCGACCCC GGTGCTCGTGTGCCCGCAGGCTGCTGTCCCCAGGGCCCAGCCTCCTCACCCCGACTGGCGACCCC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124363635..124363858 26863196 MeRIP-seq:(Medium) rs777015163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35950 Human_Splice_Rec_1441330,Human_Splice_Rec_1441422,Human_Splice_Rec_1441490,Human_Splice_Rec_1441560,Human_Splice_Rec_1441652,Human_Splice_Rec_1441798 Human_miRNA_ID_2715055,Human_miRNA_ID_3051038 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_304932,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_161519 92647 RMVar_ID_92647 Human_SNP_ID_519173035 m1A Human chr12 + 124363794 124363794 124363794 CAGTCGGGGTGAGGAGGCTGGGCCTTGGGGACAGCAGCCTGCGGGCACACGAGCACCATCAGCTG CAGTCGGGGTGAGGAGGCTGGGCCTTGGGGACGGCAGCCTGCGGGCACACGAGCACCATCAGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124363626..124363860 26863196 MeRIP-seq:(Medium) rs770082105 Functional Loss SNV dbSNP153 33..33 33 - - - 92648 RMVar_ID_92648 Human_SNP_ID_519175521 m1A Human chr12 - 124372230 124372230 124372230 GGAAGGCCGAGGAGCCCGTCAAGAGCGAGTGCACGGAGGAAGCCGAGGAGGGGCCGGCCAAGGGC GGAAGGCCGAGGAGCCCGTCAAGAGCGAGTGCGCGGAGGAAGCCGAGGAGGGGCCGGCCAAGGGC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:124371999..124372635;chr12:124372001..124372630;chr12:124372001..124372636 26863196 MeRIP-seq:(Medium) rs1383586344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35953,Human_RBP_ID_9365821,Human_RBP_ID_22532449 Human_miRNA_ID_2464983 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92649 RMVar_ID_92649 Human_SNP_ID_519175526 m1A Human chr12 - 124372239 124372239 124372239 TGGACACAGGGAAGGCCGAGGAGCCCGTCAAGAGCGAGTGCACGGAGGAAGCCGAGGAGGGGCCG TGGACACAGGGAAGGCCGAGGAGCCCGTCAAGGGCGAGTGCACGGAGGAAGCCGAGGAGGGGCCG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124372001..124372647 26863196 MeRIP-seq:(Medium) rs1407023581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35953,Human_RBP_ID_9365821,Human_RBP_ID_22532449 Human_miRNA_ID_2464983 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92650 RMVar_ID_92650 Human_SNP_ID_519175560 m1A Human chr12 - 124372301 124372301 124372301 AGCAGCGCCCCCAGTGGAGGAGGGGGAGGAGCAGAAGCCCCCCGCGGCTGAGGAGCTGGCAGTGG AGCAGCGCCCCCAGTGGAGGAGGGGGAGGAGCGGAAGCCCCCCGCGGCTGAGGAGCTGGCAGTGG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:124372152..124372385 26863196 MeRIP-seq:(Medium) rs1403180266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35953,Human_RBP_ID_26323645,Human_RBP_ID_27806231 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92651 RMVar_ID_92651 Human_SNP_ID_519175579 m1A Human chr12 - 124372349 124372337 124372349 TGCACCTCCTCCTGTGGTCCCCAAGGAGGAGAAGGAGGAGGAGACCGCAGCAGCGCCCCCAGTGG TGCACCTCCTCCTGTGGTCCCCAAGGAGGAGA____________CCGCAGCAGCGCCCCCAGTGG GTCTCCTCCTCCT G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124355401..124374418 32194978 MeRIP-seq:(Medium) rs1020305106 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_35953,Human_RBP_ID_18189278 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92652 RMVar_ID_92652 Human_SNP_ID_519175581 m1A Human chr12 - 124372349 124372341 124372350 TGCACCTCCTCCTGTGGTCCCCAAGGAGGAGAAGGAGGAGGAGACCGCAGCAGCGCCCCCAGTGG TGCACCTCCTCCTGTGGTCCCCAAGGAGGAG_________GAGACCGCAGCAGCGCCCCCAGTGG CCTCCTCCTT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124355401..124374418 32194978 MeRIP-seq:(Medium) rs1302878234 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_35953,Human_RBP_ID_18189278 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92653 RMVar_ID_92653 Human_SNP_ID_519175584 m1A Human chr12 - 124372349 124372347 124372350 TGCACCTCCTCCTGTGGTCCCCAAGGAGGAGAAGGAGGAGGAGACCGCAGCAGCGCCCCCAGTGG TGCACCTCCTCCTGTGGTCCCCAAGGAGGAG___GAGGAGGAGACCGCAGCAGCGCCCCCAGTGG CCTT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124355401..124374418 32194978 MeRIP-seq:(Medium) rs546202475 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_35953,Human_RBP_ID_18189278 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 92654 RMVar_ID_92654 Human_SNP_ID_519177663 m1A Human chr12 - 124378287 124378251 124378287 ATTCCCGCCCGTGGTGGAGGATGAGGAGATGGAGGCGTCGGGCGTGAGCGGAAATGAGGAGGAGA ATTCCCGCCCGTGGTGGAGGATGAGGAGATGG_________________________________ ACCATCTCCTCCTCATTTCCGCTCACGCCCGACGCCT A NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:124378161..124378427;chr12:124378182..124378438 26863196 MeRIP-seq:(Medium) rs779235385 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_3942411,Human_RBP_ID_4210417,Human_RBP_ID_5172692,Human_RBP_ID_5462374,Human_RBP_ID_5521878,Human_RBP_ID_8778088,Human_RBP_ID_9365822,Human_RBP_ID_17812484,Human_RBP_ID_18189279,Human_RBP_ID_18410765,Human_RBP_ID_18978186,Human_RBP_ID_19057144,Human_RBP_ID_19826121,Human_RBP_ID_22532537,Human_RBP_ID_23208309,Human_RBP_ID_24543344,Human_RBP_ID_26322334,Human_RBP_ID_27806232 Human_Splice_Rec_1441324,Human_Splice_Rec_1441325,Human_Splice_Rec_1441418,Human_Splice_Rec_1441419,Human_Splice_Rec_1441486,Human_Splice_Rec_1441487,Human_Splice_Rec_1441554,Human_Splice_Rec_1441555,Human_Splice_Rec_1441648,Human_Splice_Rec_1441649,Human_Splice_Rec_1441792,Human_Splice_Rec_1441793,Human_Splice_Rec_1441830,Human_Splice_Rec_1441831 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_49785,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 92655 RMVar_ID_92655 Human_SNP_ID_519177677 m1A Human chr12 - 124378287 124378287 124378287 ATTCCCGCCCGTGGTGGAGGATGAGGAGATGGAGGCGTCGGGCGTGAGCGGAAATGAGGAGGAGA ATTCCCGCCCGTGGTGGAGGATGAGGAGATGGCGGCGTCGGGCGTGAGCGGAAATGAGGAGGAGA T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:124378161..124378427;chr12:124378182..124378438 26863196 MeRIP-seq:(Medium) rs377686301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942411,Human_RBP_ID_4210417,Human_RBP_ID_5172692,Human_RBP_ID_5462374,Human_RBP_ID_5521878,Human_RBP_ID_8778088,Human_RBP_ID_9365822,Human_RBP_ID_17812484,Human_RBP_ID_18189279,Human_RBP_ID_18410765,Human_RBP_ID_18978186,Human_RBP_ID_19057144,Human_RBP_ID_19826121,Human_RBP_ID_22532537,Human_RBP_ID_23208309,Human_RBP_ID_24543344,Human_RBP_ID_26322334,Human_RBP_ID_27806232 Human_Splice_Rec_1441324,Human_Splice_Rec_1441325,Human_Splice_Rec_1441418,Human_Splice_Rec_1441419,Human_Splice_Rec_1441486,Human_Splice_Rec_1441487,Human_Splice_Rec_1441554,Human_Splice_Rec_1441555,Human_Splice_Rec_1441648,Human_Splice_Rec_1441649,Human_Splice_Rec_1441792,Human_Splice_Rec_1441793,Human_Splice_Rec_1441830,Human_Splice_Rec_1441831 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_49785,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 92656 RMVar_ID_92656 Human_SNP_ID_519177689 m1A Human chr12 + 124378318 124378318 124378318 CTCCATCTCCTCATCCTCCACCACGGGCGGGAATGCAGCCTCCTCGCTGGCCGCCGCCGGCGCTT CTCCATCTCCTCATCCTCCACCACGGGCGGGAGTGCAGCCTCCTCGCTGGCCGCCGCCGGCGCTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:124378251..124378425 26863196 MeRIP-seq:(Medium) rs1158575353 Functional Loss SNV dbSNP153 33..33 33 - - - 92657 RMVar_ID_92657 Human_SNP_ID_519177722 m1A Human chr12 - 124378380 124378380 124378380 CCTGATCTGCTGCTTCCCTGTGCCCCAGGAGAAGGAGAGGAACGCGCGGAGGAAGAAGAAGAAAG CCTGATCTGCTGCTTCCCTGTGCCCCAGGAGAGGGAGAGGAACGCGCGGAGGAAGAAGAAGAAAG T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124378376..124378400 26863196 MeRIP-seq:(Medium) rs760401324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521878,Human_RBP_ID_18189279,Human_RBP_ID_24543344,Human_RBP_ID_26322335,Human_RBP_ID_27807408 Human_Splice_Rec_1441324,Human_Splice_Rec_1441418,Human_Splice_Rec_1441486,Human_Splice_Rec_1441554,Human_Splice_Rec_1441648,Human_Splice_Rec_1441792,Human_Splice_Rec_1441830 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_49785,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 92658 RMVar_ID_92658 Human_SNP_ID_519179876 m1A Human chr12 - 124385696 124385696 124385696 GCTGCACCGCGCCTCTGGGAAGCTGGGAGAGGAGCCCAGACTGCCTCAGGAGATGTCTCTGCACC GCTGCACCGCGCCTCTGGGAAGCTGGGAGAGGTGCCCAGACTGCCTCAGGAGATGTCTCTGCACC T A NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:124385693..124385845;chr12:124385694..124385850 26863196 MeRIP-seq:(Medium) rs769355105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 92659 RMVar_ID_92659 Human_SNP_ID_519179897 m1A Human chr12 - 124385730 124385730 124385730 CAGCACAAGCTGAAGATGGTGAGCCCCCAGTCACGCTGCACCGCGCCTCTGGGAAGCTGGGAGAG CAGCACAAGCTGAAGATGGTGAGCCCCCAGTCGCGCTGCACCGCGCCTCTGGGAAGCTGGGAGAG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:124385726..124385800 26863196 MeRIP-seq:(Medium) rs750588014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19059735 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 92660 RMVar_ID_92660 Human_SNP_ID_519181133 m1A Human chr12 + 124389135 124389135 124389135 GGATGCCCCTGGGCCAGGTATCACCGGGGCGCAGCGTGCCGAGCTCCTCCAGCACCAATGTGCCC GGATGCCCCTGGGCCAGGTATCACCGGGGCGCGGCGTGCCGAGCTCCTCCAGCACCAATGTGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:124389132..124389310;chr12:124389130..124389279 26863196 MeRIP-seq:(Medium) rs1245945675 Functional Loss SNV dbSNP153 33..33 33 - - - 92661 RMVar_ID_92661 Human_SNP_ID_519184988 m1A Human chr12 - 124402452 124402450 124402453 AGATGAGAAGGAGAAGGAAAAGGAGGCGGAGAAGGAGGAGGAGAAGCCGGAGGTGGAGAACGACA AGATGAGAAGGAGAAGGAAAAGGAGGCGGAG___GAGGAGGAGAAGCCGGAGGTGGAGAACGACA CCTT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124402351..124402610 26863196 MeRIP-seq:(Medium) rs1418191685 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_35970,Human_RBP_ID_875407,Human_RBP_ID_3943838,Human_RBP_ID_9279360,Human_RBP_ID_18976454,Human_RBP_ID_24543214,Human_RBP_ID_26322341,Human_RBP_ID_27806236 Human_Splice_Rec_1441317,Human_Splice_Rec_1441411,Human_Splice_Rec_1441479,Human_Splice_Rec_1441547,Human_Splice_Rec_1441641,Human_Splice_Rec_1441785 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_161525,RMVar_hsa_circ_34554,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_359115,RMVar_hsa_circ_21997,RMVar_hsa_circ_123262,RMVar_hsa_circ_161521,RMVar_hsa_circ_333303,RMVar_hsa_circ_42196,RMVar_hsa_circ_356650,RMVar_hsa_circ_161522,RMVar_hsa_circ_161523,RMVar_hsa_circ_361562,RMVar_hsa_circ_376528,RMVar_hsa_circ_121865,RMVar_hsa_circ_303521,RMVar_hsa_circ_52164,RMVar_hsa_circ_161526,RMVar_hsa_circ_56917,RMVar_hsa_circ_161524 92662 RMVar_ID_92662 Human_SNP_ID_519192031 m1A Human chr12 + 124426721 124426721 124426721 TCATGGGGTCGGCCATAAGCCCGTTCATGTTGATGAACTTGATGCGCTGCTGGTCAGCGTCGTAC TCATGGGGTCGGCCATAAGCCCGTTCATGTTGCTGAACTTGATGCGCTGCTGGTCAGCGTCGTAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124426671..124426738 26863196 MeRIP-seq:(Medium) rs1367699862 Functional Loss SNV dbSNP153 33..33 33 - - - 92663 RMVar_ID_92663 Human_SNP_ID_519192944 m1A Human chr12 + 124429578 124429578 124429578 GCCTCTGCACCCTCACGGGGGATGCCAGGGAAAAGGAGCTGAGGCCAGAGTCAGGGCCTGGACTC GCCTCTGCACCCTCACGGGGGATGCCAGGGAAGAGGAGCTGAGGCCAGAGTCAGGGCCTGGACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124429576..124429656 26863196 MeRIP-seq:(Medium) rs921517910 Functional Loss SNV dbSNP153 33..33 33 - - - 92664 RMVar_ID_92664 Human_SNP_ID_519193301 m1A Human chr12 - 124430736 124430736 124430736 GCTATGACCAGCTCATGGAGGCCTGGGAGAAGAAGGTGGAGCGCATCGAGAACAACCCCCGGCGG GCTATGACCAGCTCATGGAGGCCTGGGAGAAGCAGGTGGAGCGCATCGAGAACAACCCCCGGCGG T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124429637..124430741 32194978 MeRIP-seq:(Medium) rs749576073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942416,Human_RBP_ID_9322837,Human_RBP_ID_18978192,Human_RBP_ID_23545800 Human_Splice_Rec_1441306,Human_Splice_Rec_1441400,Human_Splice_Rec_1441630,Human_Splice_Rec_1441774,Human_Splice_Rec_1441850,Human_Splice_Rec_1441872,Human_Splice_Rec_1441882 RMVar_hsa_circ_49218,RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161512,RMVar_hsa_circ_108865,RMVar_hsa_circ_161516,RMVar_hsa_circ_161525,RMVar_hsa_circ_34554,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521,RMVar_hsa_circ_333303,RMVar_hsa_circ_356650,RMVar_hsa_circ_161522,RMVar_hsa_circ_361562,RMVar_hsa_circ_376528,RMVar_hsa_circ_303521,RMVar_hsa_circ_161526,RMVar_hsa_circ_161530,RMVar_hsa_circ_289282,RMVar_hsa_circ_293667,RMVar_hsa_circ_351509,RMVar_hsa_circ_292563,RMVar_hsa_circ_67300,RMVar_hsa_circ_271831,RMVar_hsa_circ_161531,RMVar_hsa_circ_161535,RMVar_hsa_circ_322102,RMVar_hsa_circ_161528,RMVar_hsa_circ_161529,RMVar_hsa_circ_378574,RMVar_hsa_circ_283919,RMVar_hsa_circ_317072,RMVar_hsa_circ_282765,RMVar_hsa_circ_161533,RMVar_hsa_circ_161534,RMVar_hsa_circ_161532,RMVar_hsa_circ_161536,RMVar_hsa_circ_107486 92665 RMVar_ID_92665 Human_SNP_ID_519201806 m1A Human chr12 - 124459809 124459809 124459809 TGACCCTGGCGAGGAGTTTGGATTTGGTGCTCAGGGTGGCAGGAAGACAGCAGCCGAGGAGGTGA TGACCCTGGCGAGGAGTTTGGATTTGGTGCTCTGGGTGGCAGGAAGACAGCAGCCGAGGAGGTGA T A NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:124459807..124460118;chr12:124459807..124460103 26863196 MeRIP-seq:(Medium) rs1345120525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418605,Human_RBP_ID_5139981,Human_RBP_ID_8070460 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_161509,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_311834,RMVar_hsa_circ_270683,RMVar_hsa_circ_161538,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_314613,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277 92666 RMVar_ID_92666 Human_SNP_ID_519201851 m1A Human chr12 - 124459994 124459994 124459994 GTGGGGAGGGGAGGCTGAGTCAAGACATGAGCAAGAGGCAGGCGAGAGCATGTGAAGATGTGGGG GTGGGGAGGGGAGGCTGAGTCAAGACATGAGCGAGAGGCAGGCGAGAGCATGTGAAGATGTGGGG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124459943..124460072 26863196 MeRIP-seq:(Medium) rs1033207753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5171483 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_161509,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_311834,RMVar_hsa_circ_270683,RMVar_hsa_circ_161538,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_314613,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277 92667 RMVar_ID_92667 Human_SNP_ID_519203658 m1A Human chr12 + 124467001 124466998 124467001 TCACCCCCATCATCCTCATCCTCATCACCCCCATCATCCTCATCCTCACTACCCCCATCATCCTC TCACCCCCATCATCCTCATCCTCATCACCC___TCATCCTCATCCTCACTACCCCCATCATCCTC CCCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124466999..124467327 26863196 MeRIP-seq:(Medium) rs1422076943 Functional Loss DEL dbSNP153 31..33 33 - - - 92668 RMVar_ID_92668 Human_SNP_ID_519203725 m1A Human chr12 + 124467118 124467118 124467118 TCATCACCCTCATCATCCTCGTCATCCTCATGACCACCATCACCCTCATCCTCATCACCCCCATC TCATCACCCTCATCATCCTCGTCATCCTCATGCCCACCATCACCCTCATCCTCATCACCCCCATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124467115..124467214 26863196 MeRIP-seq:(Medium) rs1284493328 Functional Loss SNV dbSNP153 33..33 33 - - - 92669 RMVar_ID_92669 Human_SNP_ID_519203818 m1A Human chr12 + 124467305 124467302 124467305 ATCACCCCATCACCCTCATCCTCATCACCCTCATCCTCATCACCCCCATCATCCTCATCCTCATC ATCACCCCATCACCCTCATCCTCATCACCC___TCCTCATCACCCCCATCATCCTCATCCTCATC CTCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:124467226..124467317 26863410 MeRIP-seq:(Medium) rs1206290781 Functional Loss DEL dbSNP153 31..33 33 - - - 92670 RMVar_ID_92670 Human_SNP_ID_519204003 m1A Human chr12 + 124467693 124467691 124467694 ACCCCATCACCCTTATCATCCTCATGACCTCCATCATCCTTATCACCCTCATCATCCTCATCACC ACCCCATCACCCTTATCATCCTCATGACCTC___CATCCTTATCACCCTCATCATCCTCATCACC CCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124467691..124467782 26863196 MeRIP-seq:(Medium) rs1200942044 Functional Loss DEL dbSNP153 32..34 33 - - - 92671 RMVar_ID_92671 Human_SNP_ID_519204318 m1A Human chr12 + 124468327 124468324 124468327 CGCCCATCACCCTCATCATCCTCATCACCCTCATCATCCTCATCCTCCTCACCCCCATCATCCTC CGCCCATCACCCTCATCATCCTCATCACCC___TCATCCTCATCCTCCTCACCCCCATCATCCTC CTCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124468325..124468444 26863196 MeRIP-seq:(Medium) rs1329284111 Functional Loss DEL dbSNP153 31..33 33 - - - 92672 RMVar_ID_92672 Human_SNP_ID_519204320 m1A Human chr12 - 124468325 124468325 124468325 GGATGATGGGGGTGAGGAGGATGAGGATGATGAGGGTGATGAGGATGATGAGGGTGATGGGCGTG GGATGATGGGGGTGAGGAGGATGAGGATGATGGGGGTGATGAGGATGATGAGGGTGATGGGCGTG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124468322..124468438 26863196 MeRIP-seq:(Medium) rs1465007049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94184,RMVar_hsa_circ_161505,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_311834,RMVar_hsa_circ_270683,RMVar_hsa_circ_161538,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_314613,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277,RMVar_hsa_circ_161546,RMVar_hsa_circ_290700,RMVar_hsa_circ_294197,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110 92673 RMVar_ID_92673 Human_SNP_ID_519204537 m1A Human chr12 - 124468750 124468750 124468750 GGATGATGAGGGTGATGGGCGTGATGAGGATGAGGGTGATGAGGATGATGGGGGTGATGAGGATG GGATGATGAGGGTGATGGGCGTGATGAGGATGGGGGTGATGAGGATGATGGGGGTGATGAGGATG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124468747..124469037 26863196 MeRIP-seq:(Medium) rs1283971085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94184,RMVar_hsa_circ_161505,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_311834,RMVar_hsa_circ_270683,RMVar_hsa_circ_161538,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_314613,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277,RMVar_hsa_circ_161546,RMVar_hsa_circ_290700,RMVar_hsa_circ_294197,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110 92674 RMVar_ID_92674 Human_SNP_ID_519208664 m1A Human chr12 - 124483694 124483694 124483694 AGCTGGGGAAGTCAGAGATGGAGTTCATTGAAAGCAAGCGCCCTCGGCTAGAGCTGCTGCCTGAC AGCTGGGGAAGTCAGAGATGGAGTTCATTGAAGGCAAGCGCCCTCGGCTAGAGCTGCTGCCTGAC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124483557..124483736 26863196 MeRIP-seq:(Medium) rs183845640 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3942421,Human_RBP_ID_5554878,Human_RBP_ID_18621336 Human_Splice_Rec_1441294,Human_Splice_Rec_1441295,Human_Splice_Rec_1441388,Human_Splice_Rec_1441389,Human_Splice_Rec_1441618,Human_Splice_Rec_1441619,Human_Splice_Rec_1441762,Human_Splice_Rec_1441763,Human_Splice_Rec_1441838,Human_Splice_Rec_1441839,Human_Splice_Rec_1441861,Human_Splice_Rec_1441873 RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_290700,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_338622,RMVar_hsa_circ_161548,RMVar_hsa_circ_161549 92675 RMVar_ID_92675 Human_SNP_ID_519208682 m1A Human chr12 - 124483737 124483737 124483737 CAGGAGCTCCACCTGCGGCCAGAGTCCCACTCATACCTGCCCGAGCTGGGGAAGTCAGAGATGGA CAGGAGCTCCACCTGCGGCCAGAGTCCCACTCCTACCTGCCCGAGCTGGGGAAGTCAGAGATGGA T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124483626..124486525 32194978 MeRIP-seq:(Medium) rs993492414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3943848,Human_RBP_ID_22709973 Human_Splice_Rec_1441294,Human_Splice_Rec_1441388,Human_Splice_Rec_1441618,Human_Splice_Rec_1441762,Human_Splice_Rec_1441838 Human_miRNA_ID_2257776 RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_290700,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_338622,RMVar_hsa_circ_161548,RMVar_hsa_circ_161549 92676 RMVar_ID_92676 Human_SNP_ID_519209720 m1A Human chr12 - 124487485 124487485 124487485 CCGCAAGGCCAAGGCCAAGGCCGAGGCCCCGTAGAGAGAGGATGGGTCAGAGGAGCTTGACTCAG CCGCAAGGCCAAGGCCAAGGCCGAGGCCCCGTGGAGAGAGGATGGGTCAGAGGAGCTTGACTCAG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124487483..124487586 26863196 MeRIP-seq:(Medium) rs1407551044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92677 RMVar_ID_92677 Human_SNP_ID_519211905 m1A Human chr12 - 124495114 124495114 124495114 GTAAGGGGGTGCACATGTGTGCGCCTGGGGCTACCTTTGAGACCCTTCTTCCATTCCACTGAGTC GTAAGGGGGTGCACATGTGTGCGCCTGGGGCTGCCTTTGAGACCCTTCTTCCATTCCACTGAGTC T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124495111..124495399 26863196 MeRIP-seq:(Medium) rs773596411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92678 RMVar_ID_92678 Human_SNP_ID_519211915 m1A Human chr12 - 124495132 124495132 124495132 ATCGCCCGGACGCACACGGTAAGGGGGTGCACATGTGTGCGCCTGGGGCTACCTTTGAGACCCTT ATCGCCCGGACGCACACGGTAAGGGGGTGCACGTGTGTGCGCCTGGGGCTACCTTTGAGACCCTT T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124495126..124495150 26863196 MeRIP-seq:(Medium) rs201531964 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92679 RMVar_ID_92679 Human_SNP_ID_519211916 m1A Human chr12 - 124495132 124495132 124495132 ATCGCCCGGACGCACACGGTAAGGGGGTGCACATGTGTGCGCCTGGGGCTACCTTTGAGACCCTT ATCGCCCGGACGCACACGGTAAGGGGGTGCACCTGTGTGCGCCTGGGGCTACCTTTGAGACCCTT T G NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124495126..124495150 26863196 MeRIP-seq:(Medium) rs201531964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92680 RMVar_ID_92680 Human_SNP_ID_519211965 m1A Human chr12 - 124495225 124495225 124495225 ACCACCATGTCGGGATCCACACAGCCTGTGGCACAGACGTGGAGGGCCACTGAGCCCCGCTACCC ACCACCATGTCGGGATCCACACAGCCTGTGGCGCAGACGTGGAGGGCCACTGAGCCCCGCTACCC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124495176..124495411 26863196 MeRIP-seq:(Medium) rs994962810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114790,Human_RBP_ID_4210501,Human_RBP_ID_5521880,Human_RBP_ID_8787038,Human_RBP_ID_9279365 Human_Splice_Rec_1441291,Human_Splice_Rec_1441385,Human_Splice_Rec_1441615,Human_Splice_Rec_1441759,Human_Splice_Rec_1441835,Human_Splice_Rec_1441887 Human_miRNA_ID_2427261 RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92681 RMVar_ID_92681 Human_SNP_ID_519212018 m1A Human chr12 - 124495336 124495336 124495336 GTGCCAGTGACGGGGTGGCCCGTGAGCTGATGACGAGGACTGGCTTTTAATCCTTGGTGGTGATT GTGCCAGTGACGGGGTGGCCCGTGAGCTGATGGCGAGGACTGGCTTTTAATCCTTGGTGGTGATT T C NCOR2 Ensembl:ENSG00000196498 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124495113..124495406 26863196 MeRIP-seq:(Medium) rs548995011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114790,Human_RBP_ID_1790229,Human_RBP_ID_8778108,Human_RBP_ID_9323347,Human_RBP_ID_9365826,Human_RBP_ID_17812500,Human_RBP_ID_22573832,Human_RBP_ID_27419959 Human_Splice_Rec_1441384,Human_Splice_Rec_1441614,Human_Splice_Rec_1441758,Human_Splice_Rec_1441834,Human_Splice_Rec_1441886 RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_301571,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_161549,RMVar_hsa_circ_161550,RMVar_hsa_circ_375473 92682 RMVar_ID_92682 Human_SNP_ID_519213993 m1A Human chr12 - 124501577 124501577 124501577 GCTGCGTGGAGATAGAGGCAGAGGATGGCACGATGCATCTACAAGCCAGGGAACACCGGGGGTTG GCTGCGTGGAGATAGAGGCAGAGGATGGCACGCTGCATCTACAAGCCAGGGAACACCGGGGGTTG T G NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124501569..124501677 26863196 MeRIP-seq:(Medium) rs1278542998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21997,RMVar_hsa_circ_62283,RMVar_hsa_circ_379002 92683 RMVar_ID_92683 Human_SNP_ID_519214576 m1A Human chr12 + 124503516 124503512 124503516 TGATGGATTGATGGATGGATGGATGGATGGACAGAGGATGGACAGATGAATGGATGGATGGATGG TGATGGATTGATGGATGGATGGATGGATG____GAGGATGGACAGATGAATGGATGGATGGATGG GGACA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124503510..124503626 26863196 MeRIP-seq:(Medium) rs942152631 Functional Loss DEL dbSNP153 30..33 33 - - - 92684 RMVar_ID_92684 Human_SNP_ID_519214578 m1A Human chr12 + 124503516 124503514 124503517 TGATGGATTGATGGATGGATGGATGGATGGACAGAGGATGGACAGATGAATGGATGGATGGATGG TGATGGATTGATGGATGGATGGATGGATGGA___AGGATGGACAGATGAATGGATGGATGGATGG ACAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124503510..124503626 26863196 MeRIP-seq:(Medium) rs1436556539 Functional Loss DEL dbSNP153 32..34 33 - - - 92685 RMVar_ID_92685 Human_SNP_ID_519214583 m1A Human chr12 + 124503552 124503528 124503552 GATGGACAGATGAATGGATGGATGGATGGACGAATGGATGGATGGATAGATGGAAGACGGACGGA GATGGACAG________________________ATGGATGGATGGATAGATGGAAGACGGACGGA GATGAATGGATGGATGGATGGACGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124503549..124503670 26863196 MeRIP-seq:(Medium) rs1566004768 Functional Loss DEL dbSNP153 10..33 33 - - - 92686 RMVar_ID_92686 Human_SNP_ID_519214599 m1A Human chr12 + 124503552 124503552 124503552 GATGGACAGATGAATGGATGGATGGATGGACGAATGGATGGATGGATAGATGGAAGACGGACGGA GATGGACAGATGAATGGATGGATGGATGGACGGATGGATGGATGGATAGATGGAAGACGGACGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124503549..124503670 26863196 MeRIP-seq:(Medium) rs1294309834 Functional Loss SNV dbSNP153 33..33 33 - - - 92687 RMVar_ID_92687 Human_SNP_ID_519222630 m1A Human chr12 - 124532649 124532649 124532649 CTCCTGTGGCTGAGTTATCTGCTTGTCATGCCAGTGGCCCACCCGAGGACGATAAAAGGGCTTTT CTCCTGTGGCTGAGTTATCTGCTTGTCATGCCGGTGGCCCACCCGAGGACGATAAAAGGGCTTTT T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:124532647..124532892;chr12:124532628..124532875 26863196 MeRIP-seq:(Medium) rs1437445563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150128,Human_RBP_ID_18479803 RMVar_hsa_circ_21997,RMVar_hsa_circ_62283,RMVar_hsa_circ_379002 92688 RMVar_ID_92688 Human_SNP_ID_519224427 m1A Human chr12 - 124539223 124539221 124539223 GCCTTGAGCGAGTGAGTGGTGGGTGTGAGCACAGGGGAGCGTGACACAGCGAGTGAGACCTGCTG GCCTTGAGCGAGTGAGTGGTGGGTGTGAGCAC__GGGAGCGTGACACAGCGAGTGAGACCTGCTG CCT C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124539220..124539457 26863196 MeRIP-seq:(Medium) rs1293961208 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3418626,Human_RBP_ID_5315133,Human_RBP_ID_5644804,Human_RBP_ID_8071036,Human_RBP_ID_8177594,Human_RBP_ID_9323349,Human_RBP_ID_17243028,Human_RBP_ID_18457119 92689 RMVar_ID_92689 Human_SNP_ID_519224576 m1A Human chr12 - 124539747 124539747 124539747 GGTGCGTTTGGTAGAGTTGAGGGTAAAAGCCAACGCCAGGAGGTGGGCTTGTTTGGGAGCTGACA GGTGCGTTTGGTAGAGTTGAGGGTAAAAGCCAGCGCCAGGAGGTGGGCTTGTTTGGGAGCTGACA T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124539745..124539871 26863196 MeRIP-seq:(Medium) rs1566039092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3420859,Human_RBP_ID_8178299 92690 RMVar_ID_92690 Human_SNP_ID_519231244 m1A Human chr12 + 124562256 124562256 124562256 ACCCACTTTTCAAGTGCTCCCGAGTGACAGGCACCTAGTGGCTAAAGCACGGGACAGCGCAGCCG ACCCACTTTTCAAGTGCTCCCGAGTGACAGGCCCCTAGTGGCTAAAGCACGGGACAGCGCAGCCG A C AC073592.6 Ensembl:ENSG00000279334 Other exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124562223..124562375 26863196 MeRIP-seq:(Medium) rs1167361159 Functional Loss SNV dbSNP153 33..33 33 - - - 92691 RMVar_ID_92691 Human_SNP_ID_519232726 m1A Human chr12 - 124567525 124567525 124567525 CCGGAGCCCCGCGTCCGCCGGCGCCCCGCCCGAGCCCTGCGCCCGCGCCCTGCGCTCCGCGATGC CCGGAGCCCCGCGTCCGCCGGCGCCCCGCCCGCGCCCTGCGCCCGCGCCCTGCGCTCCGCGATGC T G NCOR2 Ensembl:ENSG00000196498 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:124567338..124567589 26863410 MeRIP-seq:(Medium) rs1266991878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247141,Human_RBP_ID_5350419,Human_RBP_ID_9279371,Human_RBP_ID_18189001 92692 RMVar_ID_92692 Human_SNP_ID_519232757 m1A Human chr12 - 124567609 124567591 124567609 CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCC__________________GGGGAGCGCGGAGCC CGGCGGCCGCGGCGGCGGT C lnc-NCOR2-5 RNACentral:URS00008BAAC8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:124567319..124567668;chr12:124567505..124567632 26863196 MeRIP-seq:(Medium) rs1351752498 Functional Loss DEL dbSNP153 33..50 33 - - - 92693 RMVar_ID_92693 Human_SNP_ID_519232765 m1A Human chr12 - 124567609 124567598 124567610 CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGC____________GGCCGCCGGGGAGCGCGGAGCC CGCGGCGGCGGTG C lnc-NCOR2-5 RNACentral:URS00008BAAC8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:124567319..124567668;chr12:124567505..124567632 26863196 MeRIP-seq:(Medium) rs1389256018 Functional Loss DEL dbSNP153 32..43 33 - - - 92694 RMVar_ID_92694 Human_SNP_ID_519232775 m1A Human chr12 - 124567609 124567600 124567609 CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCC_________GCGGCCGCCGGGGAGCGCGGAGCC CGGCGGCGGT C lnc-NCOR2-5 RNACentral:URS00008BAAC8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:124567319..124567668;chr12:124567505..124567632 26863196 MeRIP-seq:(Medium) rs1340560111 Functional Loss DEL dbSNP153 33..41 33 - - - 92695 RMVar_ID_92695 Human_SNP_ID_519232778 m1A Human chr12 - 124567609 124567603 124567609 CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCC______GCCGCGGCCGCCGGGGAGCGCGGAGCC CGGCGGT C lnc-NCOR2-5 RNACentral:URS00008BAAC8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:124567319..124567668;chr12:124567505..124567632 26863196 MeRIP-seq:(Medium) rs1232644961 Functional Loss DEL dbSNP153 33..38 33 - - - 92696 RMVar_ID_92696 Human_SNP_ID_519232784 m1A Human chr12 - 124567609 124567609 124567609 CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC CTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCGGCCGCCGGGGAGCGCGGAGCC T C lnc-NCOR2-5 RNACentral:URS00008BAAC8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:124567319..124567668;chr12:124567505..124567632 26863196 MeRIP-seq:(Medium) rs1309789246 Functional Loss SNV dbSNP153 33..33 33 - - - 92697 RMVar_ID_92697 Human_SNP_ID_519232824 m1A Human chr12 + 124567640 124567640 124567640 GTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGGGGGAGGAGGGGGCGGGGCGCGAGCCCGGGA GTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGGGGGAGGAGGGGGCGGGGCGCGAGCCCGGGA A G lnc-RFLNA-4 RNACentral:URS00008BB8F6 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:124567368..124567716 26863196 MeRIP-seq:(Medium) rs892714887 Functional Loss SNV dbSNP153 33..33 33 - - - 92698 RMVar_ID_92698 Human_SNP_ID_519287084 m1A Human chr12 - 124778037 124778037 124778037 TCTACCTGCCAGGCCAGGCAAAGCGCCTTTACACAGGCCTCGGAAAACAATGGAGTGAGCACAAG TCTACCTGCCAGGCCAGGCAAAGCGCCTTTACGCAGGCCTCGGAAAACAATGGAGTGAGCACAAG T C SCARB1 Ensembl:ENSG00000073060 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124777704..124782700 32194978 MeRIP-seq:(Medium) rs568054617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1790235,Human_RBP_ID_23546182,Human_RBP_ID_26413596 92699 RMVar_ID_92699 Human_SNP_ID_519287212 m1A Human chr12 - 124778496 124778496 124778496 GCCCCTACACCCCGCTTCTCCCGGACTCTCCCAGCGGACAGCCCCCCAGCCCCACAGCCTGAGCC GCCCCTACACCCCGCTTCTCCCGGACTCTCCCTGCGGACAGCCCCCCAGCCCCACAGCCTGAGCC T A SCARB1 Ensembl:ENSG00000073060 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124777818..124778553 26863196 MeRIP-seq:(Medium) rs1290385950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357444,Human_RBP_ID_17650922,Human_RBP_ID_18621370,Human_RBP_ID_18934882,Human_RBP_ID_22436743,Human_RBP_ID_22910647,Human_RBP_ID_27212052,Human_RBP_ID_27419990 Human_Splice_Rec_1441918,Human_Splice_Rec_1441940,Human_Splice_Rec_1441962,Human_Splice_Rec_1441964,Human_Splice_Rec_1441986,Human_Splice_Rec_1442010 Human_miRNA_ID_1356252 92700 RMVar_ID_92700 Human_SNP_ID_519289137 m1A Human chr12 + 124785937 124785937 124785937 AATTATCTTTTCTGCTGATTTACTTGGTTTTCATCTGTCTCCCCGGCTGGGATGCCAGCCCCCCT AATTATCTTTTCTGCTGATTTACTTGGTTTTCTTCTGTCTCCCCGGCTGGGATGCCAGCCCCCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124785935..124786073 26863196 MeRIP-seq:(Medium) rs1174712060 Functional Loss SNV dbSNP153 33..33 33 - - - 92701 RMVar_ID_92701 Human_SNP_ID_519289138 m1A Human chr12 - 124785938 124785938 124785938 GAGGGGGGCTGGCATCCCAGCCGGGGAGACAGATGAAAACCAAGTAAATCAGCAGAAAAGATAAT GAGGGGGGCTGGCATCCCAGCCGGGGAGACAGGTGAAAACCAAGTAAATCAGCAGAAAAGATAAT T C SCARB1 Ensembl:ENSG00000073060 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124785888..124786105 26863196 MeRIP-seq:(Medium) rs925951564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755464,Human_RBP_ID_3942424 RMVar_hsa_circ_10216,RMVar_hsa_circ_71896,RMVar_hsa_circ_161552 92702 RMVar_ID_92702 Human_SNP_ID_519289156 m1A Human chr12 - 124785979 124785979 124785979 AGCAGTAGAGGAGACAGCTGAGATCCCTGCTCAGGGGGATTGAGGGGGGCTGGCATCCCAGCCGG AGCAGTAGAGGAGACAGCTGAGATCCCTGCTCGGGGGGATTGAGGGGGGCTGGCATCCCAGCCGG T C SCARB1 Ensembl:ENSG00000073060 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124785975..124786041 26863196 MeRIP-seq:(Medium) rs2037748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150234 RMVar_hsa_circ_10216,RMVar_hsa_circ_71896 92703 RMVar_ID_92703 Human_SNP_ID_519289189 m1A Human chr12 + 124786105 124786105 124786105 ATGCAAGTACCAGGTCTCATTACTCAAAGCCCACCTGTGCCCCCTCCAAGGGAGGGTCCCAGGCC ATGCAAGTACCAGGTCTCATTACTCAAAGCCCTCCTGTGCCCCCTCCAAGGGAGGGTCCCAGGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124786092..124786295 32194978 MeRIP-seq:(Medium) rs1378166987 Functional Loss SNV dbSNP153 33..33 33 - - - 92704 RMVar_ID_92704 Human_SNP_ID_519295363 m1A Human chr12 + 124810242 124810241 124810242 TCAGGAGTCATGAAGGGCGGCCACATTTGCCCAGAAGTTCCATTGATCATGTTGCACTGATCGGA TCAGGAGTCATGAAGGGCGGCCACATTTGCCC_GAAGTTCCATTGATCATGTTGCACTGATCGGA CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124810129..124810246 26863196 MeRIP-seq:(Medium) rs749446809 Functional Loss DEL dbSNP153 33..33 33 - - - 92705 RMVar_ID_92705 Human_SNP_ID_519295364 m1A Human chr12 + 124810242 124810242 124810242 TCAGGAGTCATGAAGGGCGGCCACATTTGCCCAGAAGTTCCATTGATCATGTTGCACTGATCGGA TCAGGAGTCATGAAGGGCGGCCACATTTGCCCGGAAGTTCCATTGATCATGTTGCACTGATCGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124810129..124810246 26863196 MeRIP-seq:(Medium) rs771694795 Functional Loss SNV dbSNP153 33..33 33 - - - 92706 RMVar_ID_92706 Human_SNP_ID_519295368 m1A Human chr12 - 124810252 124810252 124810252 CTTCTGGCATTCCGATCAGTGCAACATGATCAATGGAACTTCTGGGCAAATGTGGCCGCCCTTCA CTTCTGGCATTCCGATCAGTGCAACATGATCAGTGGAACTTCTGGGCAAATGTGGCCGCCCTTCA T C SCARB1 Ensembl:ENSG00000073060 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:124810201..124810300 32194978 MeRIP-seq:(Medium) rs777634591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_873982,Human_RBP_ID_3942432,Human_RBP_ID_11870966,Human_RBP_ID_18256997,Human_RBP_ID_22756168 Human_Splice_Rec_1441904,Human_Splice_Rec_1441905,Human_Splice_Rec_1441928,Human_Splice_Rec_1441929,Human_Splice_Rec_1441950,Human_Splice_Rec_1441951,Human_Splice_Rec_1441974,Human_Splice_Rec_1441975,Human_Splice_Rec_1441996,Human_Splice_Rec_1441997,Human_Splice_Rec_1442022,Human_Splice_Rec_1442023,Human_Splice_Rec_1442042,Human_Splice_Rec_1442043 RMVar_hsa_circ_87817,RMVar_hsa_circ_71896,RMVar_hsa_circ_95970,RMVar_hsa_circ_96762,RMVar_hsa_circ_161553,RMVar_hsa_circ_161557,RMVar_hsa_circ_116316,RMVar_hsa_circ_47875,RMVar_hsa_circ_161558,RMVar_hsa_circ_161559,RMVar_hsa_circ_161560,RMVar_hsa_circ_126952,RMVar_hsa_circ_343193,RMVar_hsa_circ_288174,RMVar_hsa_circ_161563,RMVar_hsa_circ_161564,RMVar_hsa_circ_161565,RMVar_hsa_circ_161566,RMVar_hsa_circ_289491,RMVar_hsa_circ_371768,RMVar_hsa_circ_373801,RMVar_hsa_circ_371025,RMVar_hsa_circ_161568,RMVar_hsa_circ_161569,RMVar_hsa_circ_161567,RMVar_hsa_circ_161574,RMVar_hsa_circ_278562,RMVar_hsa_circ_316332,RMVar_hsa_circ_375439,RMVar_hsa_circ_375831,RMVar_hsa_circ_287041,RMVar_hsa_circ_161575,RMVar_hsa_circ_161572,RMVar_hsa_circ_161573,RMVar_hsa_circ_78746,RMVar_hsa_circ_341587,RMVar_hsa_circ_161576 92707 RMVar_ID_92707 Human_SNP_ID_519296359 m1A Human chr12 - 124814393 124814393 124814393 AGTGTCCCTTCGCCTTGCAGGGTGCGGCGGTGATGATGGAGAATAAGCCCATGACCCTGAAGCTC AGTGTCCCTTCGCCTTGCAGGGTGCGGCGGTGGTGATGGAGAATAAGCCCATGACCCTGAAGCTC T C SCARB1 Ensembl:ENSG00000073060 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124814376..124814400 26863196 MeRIP-seq:(Medium) rs200037169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_878158,Human_RBP_ID_18469261,Human_RBP_ID_22436757,Human_RBP_ID_22575530,Human_RBP_ID_22645605,Human_RBP_ID_22756174 Human_Splice_Rec_1441900,Human_Splice_Rec_1441924,Human_Splice_Rec_1441946,Human_Splice_Rec_1441970,Human_Splice_Rec_1441992,Human_Splice_Rec_1442018,Human_Splice_Rec_1442038 RMVar_hsa_circ_71896,RMVar_hsa_circ_116316,RMVar_hsa_circ_47875,RMVar_hsa_circ_161559,RMVar_hsa_circ_161560,RMVar_hsa_circ_126952,RMVar_hsa_circ_343193,RMVar_hsa_circ_161564,RMVar_hsa_circ_161565,RMVar_hsa_circ_161566,RMVar_hsa_circ_371768,RMVar_hsa_circ_373801,RMVar_hsa_circ_371025,RMVar_hsa_circ_161568,RMVar_hsa_circ_161567,RMVar_hsa_circ_161574,RMVar_hsa_circ_278562,RMVar_hsa_circ_316332,RMVar_hsa_circ_375831,RMVar_hsa_circ_161575,RMVar_hsa_circ_341587,RMVar_hsa_circ_161577,RMVar_hsa_circ_61197,RMVar_hsa_circ_277781,RMVar_hsa_circ_276245,RMVar_hsa_circ_161578,RMVar_hsa_circ_49113,RMVar_hsa_circ_304520,RMVar_hsa_circ_313850,RMVar_hsa_circ_161579,RMVar_hsa_circ_161580 92708 RMVar_ID_92708 Human_SNP_ID_519296553 m1A Human chr12 - 124815052 124815052 124815052 CAACAACAACGACACCGTGTCCTTCCTCGAGTACCGCACCTTCCAGTTCCAGCCCTCCAAGTCCC CAACAACAACGACACCGTGTCCTTCCTCGAGTTCCGCACCTTCCAGTTCCAGCCCTCCAAGTCCC T A SCARB1 Ensembl:ENSG00000073060 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:124815001..124815125 26863196 MeRIP-seq:(Medium) rs754220228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18621395,Human_RBP_ID_22436758 Human_Splice_Rec_1441898,Human_Splice_Rec_1441899,Human_Splice_Rec_1441922,Human_Splice_Rec_1441923,Human_Splice_Rec_1441944,Human_Splice_Rec_1441945,Human_Splice_Rec_1441968,Human_Splice_Rec_1441969,Human_Splice_Rec_1441990,Human_Splice_Rec_1441991,Human_Splice_Rec_1442016,Human_Splice_Rec_1442017,Human_Splice_Rec_1442036,Human_Splice_Rec_1442037,Human_Splice_Rec_1442056,Human_Splice_Rec_1442060,Human_Splice_Rec_1442066 Human_miRNA_ID_2143710,Human_miRNA_ID_2145241,Human_miRNA_ID_2687742 RMVar_hsa_circ_71896,RMVar_hsa_circ_116316,RMVar_hsa_circ_47875,RMVar_hsa_circ_161559,RMVar_hsa_circ_161560,RMVar_hsa_circ_126952,RMVar_hsa_circ_343193,RMVar_hsa_circ_161564,RMVar_hsa_circ_161565,RMVar_hsa_circ_161566,RMVar_hsa_circ_371768,RMVar_hsa_circ_371025,RMVar_hsa_circ_161567,RMVar_hsa_circ_278562,RMVar_hsa_circ_316332,RMVar_hsa_circ_161575,RMVar_hsa_circ_341587,RMVar_hsa_circ_161577,RMVar_hsa_circ_277781,RMVar_hsa_circ_276245,RMVar_hsa_circ_161578,RMVar_hsa_circ_304520,RMVar_hsa_circ_313850,RMVar_hsa_circ_161579,RMVar_hsa_circ_161580 92709 RMVar_ID_92709 Human_SNP_ID_519296571 m1A Human chr12 - 124815079 124815079 124815079 GTTCAGGCACAAAAGCAACATCACCTTCAACAACAACGACACCGTGTCCTTCCTCGAGTACCGCA GTTCAGGCACAAAAGCAACATCACCTTCAACAGCAACGACACCGTGTCCTTCCTCGAGTACCGCA T C SCARB1 Ensembl:ENSG00000073060 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124814945..124815165 26863196 MeRIP-seq:(Medium) rs948517892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2311978,Human_RBP_ID_17236919,Human_RBP_ID_17352598,Human_RBP_ID_17469104,Human_RBP_ID_27420005 Human_Splice_Rec_1441898,Human_Splice_Rec_1441922,Human_Splice_Rec_1441944,Human_Splice_Rec_1441968,Human_Splice_Rec_1441990,Human_Splice_Rec_1442016,Human_Splice_Rec_1442036,Human_Splice_Rec_1442056,Human_Splice_Rec_1442060,Human_Splice_Rec_1442066 Human_miRNA_ID_1959227,Human_miRNA_ID_2977376 RMVar_hsa_circ_71896,RMVar_hsa_circ_116316,RMVar_hsa_circ_47875,RMVar_hsa_circ_161559,RMVar_hsa_circ_161560,RMVar_hsa_circ_126952,RMVar_hsa_circ_343193,RMVar_hsa_circ_161564,RMVar_hsa_circ_161565,RMVar_hsa_circ_161566,RMVar_hsa_circ_371768,RMVar_hsa_circ_371025,RMVar_hsa_circ_161567,RMVar_hsa_circ_278562,RMVar_hsa_circ_316332,RMVar_hsa_circ_161575,RMVar_hsa_circ_341587,RMVar_hsa_circ_161577,RMVar_hsa_circ_277781,RMVar_hsa_circ_276245,RMVar_hsa_circ_161578,RMVar_hsa_circ_304520,RMVar_hsa_circ_313850,RMVar_hsa_circ_161579,RMVar_hsa_circ_161580 92710 RMVar_ID_92710 Human_SNP_ID_519297421 m1A Human chr12 + 124817652 124817652 124817652 CGTCAAAGAAGTAGACGGAGAGATAGAAGGGGATAGGGATCTCCTTCCACATGTTGAAGGACAGG CGTCAAAGAAGTAGACGGAGAGATAGAAGGGGGTAGGGATCTCCTTCCACATGTTGAAGGACAGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:124817474..124817760;chr12:124817468..124817811 26863196 MeRIP-seq:(Medium) rs367868503 Functional Loss SNV dbSNP153 33..33 33 - - - 92711 RMVar_ID_92711 Human_SNP_ID_519303818 m1A Human chr12 + 124841592 124841592 124841592 CTGAACTCCTCCAGGTGTCCTGCAAGGCCCCCACATGCCTGTCCCCTTTCACCCCCTCCAGTCAC CTGAACTCCTCCAGGTGTCCTGCAAGGCCCCCTCATGCCTGTCCCCTTTCACCCCCTCCAGTCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124841590..124841903 26863196 MeRIP-seq:(Medium) rs571456879 Functional Loss SNV dbSNP153 33..33 33 - - - 92712 RMVar_ID_92712 Human_SNP_ID_519322426 m1A Human chr12 + 124911831 124911831 124911831 AGCTGTTTCCCAGCAAAGATCAACCTCTGCTGATCAGGAGGGATGCCTTCCTTATCTTGGATCTT AGCTGTTTCCCAGCAAAGATCAACCTCTGCTGGTCAGGAGGGATGCCTTCCTTATCTTGGATCTT A G HSALNG0094859 RNACentral:URS0000EB0431 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124911693..124911866 26863196 MeRIP-seq:(Medium) rs16918544 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_12087 92713 RMVar_ID_92713 Human_SNP_ID_519322482 m1A Human chr12 - 124911942 124911942 124911942 CACCTGGTGCTCCGTCTCAGAGGTGGGATGCAAATCTTCGTGAAGACCCTGACTGGTAAGACCAT CACCTGGTGCTCCGTCTCAGAGGTGGGATGCAGATCTTCGTGAAGACCCTGACTGGTAAGACCAT T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1071727 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_2157713 RMVar_hsa_circ_94375,RMVar_hsa_circ_95999,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161583,RMVar_hsa_circ_92676,RMVar_hsa_circ_161582,RMVar_hsa_circ_100069,RMVar_hsa_circ_161584,RMVar_hsa_circ_161585 92714 RMVar_ID_92714 Human_SNP_ID_519322698 m1A Human chr12 - 124912671 124912671 124912671 GGTCGTACCCTGTCTGACTACAACATCCAGAAAGAGTCCACCTTGCACCTGGTGCTCCGTCTCAG GGTCGTACCCTGTCTGACTACAACATCCAGAAGGAGTCCACCTTGCACCTGGTGCTCCGTCTCAG T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1203640792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1790258,Human_RBP_ID_5171557,Human_RBP_ID_9255617,Human_RBP_ID_18189004,Human_RBP_ID_18621418,Human_RBP_ID_22171688,Human_RBP_ID_27420014 Human_miRNA_ID_2697487 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_92676,RMVar_hsa_circ_161582,RMVar_hsa_circ_161585 92715 RMVar_ID_92715 Human_SNP_ID_519322720 m1A Human chr12 - 124912716 124912716 124912716 CCTGACCAGCAGAGGTTGATCTTTGCCGGAAAACAGCTGGAAGATGGTCGTACCCTGTCTGACTA CCTGACCAGCAGAGGTTGATCTTTGCCGGAAAGCAGCTGGAAGATGGTCGTACCCTGTCTGACTA T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11537764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229097,Human_RBP_ID_4252182,Human_RBP_ID_24543217,Human_RBP_ID_26322357 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_92676,RMVar_hsa_circ_161582,RMVar_hsa_circ_161585 92716 RMVar_ID_92716 Human_SNP_ID_519322833 m1A Human chr12 - 124913007 124913007 124913007 GTCGAGCCCAGTGACACTATCGAGAACGTCAAAGCAAAGATCCAAGACAAGGAAGGCATTCCTCC GTCGAGCCCAGTGACACTATCGAGAACGTCAAGGCAAAGATCCAAGACAAGGAAGGCATTCCTCC T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124912956..124913225 26863196 MeRIP-seq:(Medium) rs116167503 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_35136,Human_RBP_ID_1467387,Human_RBP_ID_1790259,Human_RBP_ID_3397568,Human_RBP_ID_8369135,Human_RBP_ID_8787464,Human_RBP_ID_9255621,Human_RBP_ID_9279376,Human_RBP_ID_24543218,Human_RBP_ID_26413633,Human_RBP_ID_26807307,Human_RBP_ID_27807429 Human_miRNA_ID_1264451,Human_miRNA_ID_1269541,Human_miRNA_ID_1697215 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161585 92717 RMVar_ID_92717 Human_SNP_ID_519323024 m1A Human chr12 + 124913455 124913455 124913455 GCTGGTCAGGAGGAATGCCTTCCTTGTCCTGGATCTTTGCTTTGACGTTCTCGATGGTGTCACTG GCTGGTCAGGAGGAATGCCTTCCTTGTCCTGGGTCTTTGCTTTGACGTTCTCGATGGTGTCACTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:124913401..124913802 32194978 MeRIP-seq:(Medium) rs1411146710 Functional Loss SNV dbSNP153 33..33 33 - - - 92718 RMVar_ID_92718 Human_SNP_ID_519323027 m1A Human chr12 - 124913463 124913463 124913463 GTCGAGCCCAGTGACACCATCGAGAACGTCAAAGCAAAGATCCAGGACAAGGAAGGCATTCCTCC GTCGAGCCCAGTGACACCATCGAGAACGTCAAGGCAAAGATCCAGGACAAGGAAGGCATTCCTCC T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs576419569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35138,Human_RBP_ID_753917,Human_RBP_ID_990514,Human_RBP_ID_1467393,Human_RBP_ID_1790263,Human_RBP_ID_3397570,Human_RBP_ID_4210735,Human_RBP_ID_6150339,Human_RBP_ID_8369136,Human_RBP_ID_8778124,Human_RBP_ID_11871302,Human_RBP_ID_17812541,Human_RBP_ID_18257001,Human_RBP_ID_18527564,Human_RBP_ID_18621420,Human_RBP_ID_22900692,Human_RBP_ID_23305718,Human_RBP_ID_24543220,Human_RBP_ID_26322360,Human_RBP_ID_26609575,Human_RBP_ID_26903499,Human_RBP_ID_27212081 Human_miRNA_ID_2255125 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161585 92719 RMVar_ID_92719 Human_SNP_ID_519323134 m1A Human chr12 + 124913722 124913722 124913722 CCTTGACATTCTCGATGGTGTCACTGGGCTCAACCTCGAGGGTGATGGTCTTACCAGTCAGAGTC CCTTGACATTCTCGATGGTGTCACTGGGCTCAGCCTCGAGGGTGATGGTCTTACCAGTCAGAGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124913578..124913779 26863196 MeRIP-seq:(Medium) rs1429145940 Functional Loss SNV dbSNP153 33..33 33 - - - 92720 RMVar_ID_92720 Human_SNP_ID_519323623 m1A Human chr12 - 124914580 124914580 124914580 TTGTGGATCGCTGTGATCGTCACTTGGTGAGTAGCGGGCTGCTGGGCTGGCCGGGGCTTTCGTGG TTGTGGATCGCTGTGATCGTCACTTGGTGAGTGGCGGGCTGCTGGGCTGGCCGGGGCTTTCGTGG T C UBC Ensembl:ENSG00000150991 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:124914576..124914650 32194978 MeRIP-seq:(Medium) rs1458084575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753924,Human_RBP_ID_1480039,Human_RBP_ID_1790271,Human_RBP_ID_4252204,Human_RBP_ID_5171564,Human_RBP_ID_5347027,Human_RBP_ID_6150344,Human_RBP_ID_18417627,Human_RBP_ID_18621424,Human_RBP_ID_19057155,Human_RBP_ID_22039725,Human_RBP_ID_22171701,Human_RBP_ID_22354602,Human_RBP_ID_22710388,Human_RBP_ID_23113357,Human_RBP_ID_26776941 RMVar_hsa_circ_94375,RMVar_hsa_circ_161581 92721 RMVar_ID_92721 Human_SNP_ID_519323633 m1A Human chr12 - 124914597 124914597 124914597 TGGGTCGCAGTTCTTGTTTGTGGATCGCTGTGATCGTCACTTGGTGAGTAGCGGGCTGCTGGGCT TGGGTCGCAGTTCTTGTTTGTGGATCGCTGTGGTCGTCACTTGGTGAGTAGCGGGCTGCTGGGCT T C UBC Ensembl:ENSG00000150991 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124914350..124914650 26863196 MeRIP-seq:(Medium) rs1333986884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275113,Human_RBP_ID_753925,Human_RBP_ID_1165456,Human_RBP_ID_1467406,Human_RBP_ID_1790272,Human_RBP_ID_4210747,Human_RBP_ID_8787468,Human_RBP_ID_9255627,Human_RBP_ID_18189011,Human_RBP_ID_18417627,Human_RBP_ID_19059750,Human_RBP_ID_22039726,Human_RBP_ID_22436171,Human_RBP_ID_23113357,Human_RBP_ID_23207933,Human_RBP_ID_23546280,Human_RBP_ID_26903504,Human_RBP_ID_27212091 Human_Splice_Rec_1442071,Human_Splice_Rec_1442075,Human_Splice_Rec_1442079,Human_Splice_Rec_1442099,Human_Splice_Rec_1442103 RMVar_hsa_circ_94375,RMVar_hsa_circ_161581 92722 RMVar_ID_92722 Human_SNP_ID_519327522 m1A Human chr12 - 124927360 124927360 124927360 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGCCAAGTACGTTTTTAC TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGGCCAAGTACGTTTTTAC T C tRNA-Asp-GTC-2-1,AB330774-001,AB330774-001:2,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00000711F0,RNACentral:URS00002B094D,RNACentral:URS00005EA0AD tRNA,misc_RNA,misc_RNA,tRNA intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1446806586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414491,Human_RBP_ID_1165460,Human_RBP_ID_1356586,Human_RBP_ID_1467414,Human_RBP_ID_5461550,Human_RBP_ID_6150354,Human_RBP_ID_8369150,Human_RBP_ID_9012932,Human_RBP_ID_9669856,Human_RBP_ID_17812544,Human_RBP_ID_18206514,Human_RBP_ID_18433808,Human_RBP_ID_18621431,Human_RBP_ID_19701967,Human_RBP_ID_22002019,Human_RBP_ID_22492667,Human_RBP_ID_22793498,Human_RBP_ID_23125266,Human_RBP_ID_23156730,Human_RBP_ID_23546283,Human_RBP_ID_26748136,Human_RBP_ID_27557765,Human_RBP_ID_27624541 92723 RMVar_ID_92723 Human_SNP_ID_519327593 m1A Human chr12 - 124927408 124927408 124927408 TTGAAGAACCTGTTTTATGGGCGGTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG TTGAAGAACCTGTTTTATGGGCGGTCCTCGTTGGTATAGTGGTGAGTATCCCCGCCTGTCACGCG T C tRNA-Asp-GTC-2-1,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00005EA0AD tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs970372691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414493,Human_RBP_ID_990518,Human_RBP_ID_1165461,Human_RBP_ID_1356587,Human_RBP_ID_1467416,Human_RBP_ID_1790277,Human_RBP_ID_6150355,Human_RBP_ID_8247545,Human_RBP_ID_8369151,Human_RBP_ID_8778129,Human_RBP_ID_9012933,Human_RBP_ID_11871324,Human_RBP_ID_17683741,Human_RBP_ID_17812545,Human_RBP_ID_18433809,Human_RBP_ID_18621433,Human_RBP_ID_23125268,Human_RBP_ID_23546287,Human_RBP_ID_26609576,Human_RBP_ID_27154688,Human_RBP_ID_27624542 92724 RMVar_ID_92724 Human_SNP_ID_519327618 m1A Human chr12 - 124927424 124927424 124927424 ACCTTAAAACAGTCTCTTGAAGAACCTGTTTTATGGGCGGTCCTCGTTAGTATAGTGGTGAGTAT ACCTTAAAACAGTCTCTTGAAGAACCTGTTTTGTGGGCGGTCCTCGTTAGTATAGTGGTGAGTAT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:124927338..124927486 26863196 MeRIP-seq:(Medium) rs977620387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_990518,Human_RBP_ID_1356588,Human_RBP_ID_1467417,Human_RBP_ID_1790277,Human_RBP_ID_4210765,Human_RBP_ID_6150355,Human_RBP_ID_8369152,Human_RBP_ID_8778129,Human_RBP_ID_9012933,Human_RBP_ID_11871324,Human_RBP_ID_17683743,Human_RBP_ID_17812546,Human_RBP_ID_18621433,Human_RBP_ID_22171706,Human_RBP_ID_23125269,Human_RBP_ID_23546287,Human_RBP_ID_26903510,Human_RBP_ID_27154688,Human_RBP_ID_27624543 92725 RMVar_ID_92725 Human_SNP_ID_519327868 m1A Human chr12 - 124927858 124927858 124927858 GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACTTCCTCTTTTTCCTTC GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGGTCCCGGGTTTCGGCACTTCCTCTTTTTCCTTC T C TRF-GAA1-1,TRF-GAA1-1:2,piR-43773,TRF-GAA1-1:3,TRF-GAA1-1:4,lnc-UBC-3,tRNA-Phe-GAA-1-3 RNACentral:URS0000632456,RNACentral:URS00001CE4E0,RNACentral:URS00004CEA14,RNACentral:URS00006A7E04,RNACentral:URS00006D05AC,RNACentral:URS0000D5BF17,RNACentral:URS000029CCC5 tRNA,tRNA,piRNA,tRNA,tRNA,lincRNA,tRNA intron,intron,intron,intron,intron,intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1382117447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414494,Human_RBP_ID_1128009,Human_RBP_ID_1165463,Human_RBP_ID_1267846,Human_RBP_ID_1356589,Human_RBP_ID_1480042,Human_RBP_ID_1790279,Human_RBP_ID_3397577,Human_RBP_ID_4210767,Human_RBP_ID_5257069,Human_RBP_ID_5273932,Human_RBP_ID_5416786,Human_RBP_ID_5461552,Human_RBP_ID_5560853,Human_RBP_ID_6150357,Human_RBP_ID_8066326,Human_RBP_ID_8247547,Human_RBP_ID_8369154,Human_RBP_ID_8778131,Human_RBP_ID_9012934,Human_RBP_ID_11871325,Human_RBP_ID_17586769,Human_RBP_ID_17683744,Human_RBP_ID_17812547,Human_RBP_ID_18257003,Human_RBP_ID_18433810,Human_RBP_ID_18511078,Human_RBP_ID_18526533,Human_RBP_ID_18621435,Human_RBP_ID_19736772,Human_RBP_ID_22793500,Human_RBP_ID_23125274,Human_RBP_ID_23582374,Human_RBP_ID_26747969,Human_RBP_ID_27154693 92726 RMVar_ID_92726 Human_SNP_ID_519331384 m1A Human chr12 - 124939662 124939662 124939662 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGCCGGGTACTTTCGTAT TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGGCCGGGTACTTTCGTAT T C tRNA-Asp-GTC-2-1,AB330774-001,AB330774-001:2,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00000711F0,RNACentral:URS00002B094D,RNACentral:URS00005EA0AD tRNA,misc_RNA,misc_RNA,tRNA exon,intron,intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1033637936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1165464,Human_RBP_ID_1467424,Human_RBP_ID_8247550,Human_RBP_ID_11871349,Human_RBP_ID_17812549,Human_RBP_ID_18199239,Human_RBP_ID_23125280,Human_RBP_ID_26748183,Human_RBP_ID_27154697 92727 RMVar_ID_92727 Human_SNP_ID_519331471 m1A Human chr12 - 124939710 124939710 124939710 CTGCAGGGAACACAGTACGGCTTGTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG CTGCAGGGAACACAGTACGGCTTGTCCTCGTTTGTATAGTGGTGAGTATCCCCGCCTGTCACGCG T A tRNA-Asp-GTC-2-1,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00005EA0AD tRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs970133733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1467428,Human_RBP_ID_5274081,Human_RBP_ID_5560852,Human_RBP_ID_8369162,Human_RBP_ID_11871351,Human_RBP_ID_17358718,Human_RBP_ID_18621443,Human_RBP_ID_23125282,Human_RBP_ID_23546294,Human_RBP_ID_26609579,Human_RBP_ID_26748169 92728 RMVar_ID_92728 Human_SNP_ID_519331472 m1A Human chr12 - 124939710 124939710 124939710 CTGCAGGGAACACAGTACGGCTTGTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG CTGCAGGGAACACAGTACGGCTTGTCCTCGTTGGTATAGTGGTGAGTATCCCCGCCTGTCACGCG T C tRNA-Asp-GTC-2-1,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00005EA0AD tRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs970133733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1467428,Human_RBP_ID_5274081,Human_RBP_ID_5560852,Human_RBP_ID_8369162,Human_RBP_ID_11871351,Human_RBP_ID_17358718,Human_RBP_ID_18621443,Human_RBP_ID_23125282,Human_RBP_ID_23546294,Human_RBP_ID_26609579,Human_RBP_ID_26748169 92729 RMVar_ID_92729 Human_SNP_ID_519331763 m1A Human chr12 + 124940022 124940010 124940023 GCATGCTTTGCACGTATGAGGCCCCGGGTTCAATCCCCGGCATCTCCAGACTTTTCCGCCTTTTT GCATGCTTTGCACGTATGAGG_____________CCCCGGCATCTCCAGACTTTTCCGCCTTTTT GCCCCGGGTTCAAT G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1566314239 Functional Loss DEL dbSNP153 22..34 33 - - - 92730 RMVar_ID_92730 Human_SNP_ID_519331783 m1A Human chr12 + 124940022 124940022 124940022 GCATGCTTTGCACGTATGAGGCCCCGGGTTCAATCCCCGGCATCTCCAGACTTTTCCGCCTTTTT GCATGCTTTGCACGTATGAGGCCCCGGGTTCAGTCCCCGGCATCTCCAGACTTTTCCGCCTTTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs768586678 Functional Loss SNV dbSNP153 33..33 33 - - - 92731 RMVar_ID_92731 Human_SNP_ID_519334646 m1A Human chr12 - 124950243 124950243 124950243 GGGTCCCTGTCTCACTGGCTCCCACCTTCTAGATCGCGTGGGCTGGCCGCTCCCCGCCATCGAGG GGGTCCCTGTCTCACTGGCTCCCACCTTCTAGTTCGCGTGGGCTGGCCGCTCCCCGCCATCGAGG T A DHX37 Ensembl:ENSG00000150990 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124950223..124950543 32194978 MeRIP-seq:(Medium) rs927709664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8369177,Human_RBP_ID_26807312 Human_Splice_Rec_1442108,Human_Splice_Rec_1442109,Human_Splice_Rec_1442160,Human_Splice_Rec_1442161,Human_Splice_Rec_1442206,Human_Splice_Rec_1442207 RMVar_hsa_circ_97516,RMVar_hsa_circ_118039,RMVar_hsa_circ_113657,RMVar_hsa_circ_161587,RMVar_hsa_circ_161588,RMVar_hsa_circ_161589 92732 RMVar_ID_92732 Human_SNP_ID_519334647 m1A Human chr12 - 124950243 124950243 124950243 GGGTCCCTGTCTCACTGGCTCCCACCTTCTAGATCGCGTGGGCTGGCCGCTCCCCGCCATCGAGG GGGTCCCTGTCTCACTGGCTCCCACCTTCTAGGTCGCGTGGGCTGGCCGCTCCCCGCCATCGAGG T C DHX37 Ensembl:ENSG00000150990 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124950223..124950543 32194978 MeRIP-seq:(Medium) rs927709664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8369177,Human_RBP_ID_26807312 Human_Splice_Rec_1442108,Human_Splice_Rec_1442109,Human_Splice_Rec_1442160,Human_Splice_Rec_1442161,Human_Splice_Rec_1442206,Human_Splice_Rec_1442207 RMVar_hsa_circ_97516,RMVar_hsa_circ_118039,RMVar_hsa_circ_113657,RMVar_hsa_circ_161587,RMVar_hsa_circ_161588,RMVar_hsa_circ_161589 92733 RMVar_ID_92733 Human_SNP_ID_519335306 m1A Human chr12 - 124952473 124952473 124952473 CAGGTGACCTACCTGCGACAGATCGTGACGGCAGGCCTGGGGGACCACTTGGCCCGCAGGGTCCA CAGGTGACCTACCTGCGACAGATCGTGACGGCGGGCCTGGGGGACCACTTGGCCCGCAGGGTCCA T C DHX37 Ensembl:ENSG00000150990 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4429156 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_229092,Human_RBP_ID_8787042 Human_Splice_Rec_1442105,Human_Splice_Rec_1442154,Human_Splice_Rec_1442155,Human_Splice_Rec_1442200,Human_Splice_Rec_1442201 RMVar_hsa_circ_97516,RMVar_hsa_circ_118039,RMVar_hsa_circ_161587,RMVar_hsa_circ_28697,RMVar_hsa_circ_107808,RMVar_hsa_circ_161589,RMVar_hsa_circ_306387,RMVar_hsa_circ_50710,RMVar_hsa_circ_161590 92734 RMVar_ID_92734 Human_SNP_ID_519339200 m1A Human chr12 - 124965003 124965003 124965003 GGTGCCAGTGACCTCTGCTTTCCCTCCAGGTGAGCAGCCGGATGCCTCCCTCCCGCTCCACGTGC GGTGCCAGTGACCTCTGCTTTCCCTCCAGGTGGGCAGCCGGATGCCTCCCTCCCGCTCCACGTGC T C DHX37 Ensembl:ENSG00000150990 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124964977..124966917 32194978 MeRIP-seq:(Medium) rs757544001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_810338,Human_RBP_ID_3942439,Human_RBP_ID_18978210 Human_Splice_Rec_1442140,Human_Splice_Rec_1442141,Human_Splice_Rec_1442186,Human_Splice_Rec_1442187,Human_Splice_Rec_1442216,Human_Splice_Rec_1442217 RMVar_hsa_circ_97516,RMVar_hsa_circ_161587,RMVar_hsa_circ_71382,RMVar_hsa_circ_82982,RMVar_hsa_circ_107808,RMVar_hsa_circ_50710,RMVar_hsa_circ_161590,RMVar_hsa_circ_110692,RMVar_hsa_circ_161591,RMVar_hsa_circ_119770,RMVar_hsa_circ_161595,RMVar_hsa_circ_73533,RMVar_hsa_circ_161594,RMVar_hsa_circ_15905,RMVar_hsa_circ_161596,RMVar_hsa_circ_11460,RMVar_hsa_circ_374926,RMVar_hsa_circ_293941,RMVar_hsa_circ_347256,RMVar_hsa_circ_126719,RMVar_hsa_circ_161597,RMVar_hsa_circ_161598,RMVar_hsa_circ_161599,RMVar_hsa_circ_111581 92735 RMVar_ID_92735 Human_SNP_ID_519344049 m1A Human chr12 - 124980731 124980731 124980731 CTGGCCCTCAGCTGAGGAGGAGGAGGAGGAGGAGGAGGAGTCGGAATCGGAGCTGGAGGAGGAGT CTGGCCCTCAGCTGAGGAGGAGGAGGAGGAGGCGGAGGAGTCGGAATCGGAGCTGGAGGAGGAGT T G DHX37 Ensembl:ENSG00000150990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124980683..124980805 26863196 MeRIP-seq:(Medium) rs780779636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811549,Human_RBP_ID_26322364 RMVar_hsa_circ_73533,RMVar_hsa_circ_120739,RMVar_hsa_circ_161604,RMVar_hsa_circ_9280,RMVar_hsa_circ_303576,RMVar_hsa_circ_313598 92736 RMVar_ID_92736 Human_SNP_ID_519346345 m1A Human chr12 - 124989071 124989071 124989071 TGGTCTGGGAACCCACGTGGGCTGGGTTTCGGATTGCTCTGCTGGTCCGGCCGCTGGAGCGCCCA TGGTCTGGGAACCCACGTGGGCTGGGTTTCGGCTTGCTCTGCTGGTCCGGCCGCTGGAGCGCCCA T G DHX37 Ensembl:ENSG00000150990 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124988982..124989072 26863196 MeRIP-seq:(Medium) rs1400182025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247144,Human_RBP_ID_9365833 RMVar_hsa_circ_120739,RMVar_hsa_circ_161604 92737 RMVar_ID_92737 Human_SNP_ID_519347758 m1A Human chr12 + 124993726 124993726 124993726 GCCCCCGAGCGCGCCAACCTTGCCCTAGCCGGAGCCCGCTGCGGCCCAGCGCACGGCCCTCACCC GCCCCCGAGCGCGCCAACCTTGCCCTAGCCGGGGCCCGCTGCGGCCCAGCGCACGGCCCTCACCC A G BRI3BP Ensembl:ENSG00000184992 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124993676..124994004 26863196 MeRIP-seq:(Medium) rs1437987980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210862,Human_RBP_ID_22436769 92738 RMVar_ID_92738 Human_SNP_ID_519347772 m1A Human chr12 + 124993755 124993755 124993755 CGGAGCCCGCTGCGGCCCAGCGCACGGCCCTCACCCCGCATCGCGACCCCGCGCCCCGCCGGCCG CGGAGCCCGCTGCGGCCCAGCGCACGGCCCTCCCCCCGCATCGCGACCCCGCGCCCCGCCGGCCG A C BRI3BP Ensembl:ENSG00000184992 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:124993656..124993773 26863410 MeRIP-seq:(Medium) rs946046783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4210862,Human_RBP_ID_22436769 92739 RMVar_ID_92739 Human_SNP_ID_519347869 m1A Human chr12 + 124993915 124993915 124993915 CGCGCAGGGGGCGCGGGGCCGCGGCGGCGCGGAGAAGAACAGCTACCGCCGCACGGTCAACACCT CGCGCAGGGGGCGCGGGGCCGCGGCGGCGCGGGGAAGAACAGCTACCGCCGCACGGTCAACACCT A G BRI3BP Ensembl:ENSG00000184992 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:124993686..124993963 26863196 MeRIP-seq:(Medium) rs751236717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4248016,Human_RBP_ID_22436770 Human_Splice_Rec_1442219,Human_Splice_Rec_1442223,Human_Splice_Rec_1442227 92740 RMVar_ID_92740 Human_SNP_ID_519366578 m1A Human chr12 + 125065598 125065597 125065598 CCGGCCGCCCGCCGCCGCCATGTCCAAGGAGGAGCGCCCCGGTCGGGAGGAGATCCTGGAGTGCC CCGGCCGCCCGCCGCCGCCATGTCCAAGGAGG_GCGCCCCGGTCGGGAGGAGATCCTGGAGTGCC GA G AACS Ensembl:ENSG00000081760 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:125065491..125065675 26863196 MeRIP-seq:(Medium) rs1565916511 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_810314,Human_RBP_ID_9322860 92741 RMVar_ID_92741 Human_SNP_ID_519386943 m1A Human chr12 - 125142778 125142778 125142778 GGTGACGCACAGTCCTCCAGGGCCTGCATTGCATCCATGACACAGACACACGTGAACACCCAGCC GGTGACGCACAGTCCTCCAGGGCCTGCATTGCGTCCATGACACAGACACACGTGAACACCCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:125142727..125142847 26863196 MeRIP-seq:(Medium) rs1246528549 Functional Loss SNV dbSNP153 33..33 33 - - - 92742 RMVar_ID_92742 Human_SNP_ID_519884462 m1A Human chr12 + 127130032 127130032 127130032 TCCTCAGCTCAGAGGCGGATCAATGTACAAGAACAAATAAAATATGGAAAGACAGATACAGTTTT TCCTCAGCTCAGAGGCGGATCAATGTACAAGAGCAAATAAAATATGGAAAGACAGATACAGTTTT A G AC079949.3 Ensembl:ENSG00000286016 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:127129973..127130045 26863196 MeRIP-seq:(Medium) rs937778441 Functional Loss SNV dbSNP153 33..33 33 - - - 92743 RMVar_ID_92743 Human_SNP_ID_519888265 m1A Human chr12 + 127146331 127146331 127146331 GGTCGCAGCCTCAGGACCCGGAGGATGTGCCCAGCACCTCCAGGAGACGCGCGGACGAGGTCGTC GGTCGCAGCCTCAGGACCCGGAGGATGTGCCCCGCACCTCCAGGAGACGCGCGGACGAGGTCGTC A C AC079949.3 Ensembl:ENSG00000286016 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:127146282..127146437 26863196 MeRIP-seq:(Medium) rs1303481981 Functional Loss SNV dbSNP153 33..33 33 - - - 92744 RMVar_ID_92744 Human_SNP_ID_519892889 m1A Human chr12 + 127166018 127166018 127166018 AGAAGCAAGTCGTCTACGAATGGTTTAGCGCCAGGTTCCCCACGAACGTGCGTTGCGTGACGGGC AGAAGCAAGTCGTCTACGAATGGTTTAGCGCCGGGTTCCCCACGAACGTGCGTTGCGTGACGGGC A G AC079949.3 Ensembl:ENSG00000286016 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:127166001..127166025 26863196 MeRIP-seq:(Medium) rs897764340 Functional Loss SNV dbSNP153 33..33 33 - - - 92745 RMVar_ID_92745 Human_SNP_ID_519892902 m1A Human chr12 - 127166043 127166043 127166043 CGGCCGGAAAGGCGGCCGCCCTCTCGCCCGTCACGCAACGCACGTTCGTGGGGAACCTGGCGCTA CGGCCGGAAAGGCGGCCGCCCTCTCGCCCGTCGCGCAACGCACGTTCGTGGGGAACCTGGCGCTA T C lnc-SLC15A4-24 RNACentral:URS00008C3198 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:127166001..127166108;chr12:127165963..127166121;chr12:127166001..127166075 26863196 MeRIP-seq:(Medium) rs556285089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269446,Human_RBP_ID_275124,Human_RBP_ID_414701,Human_RBP_ID_1082790,Human_RBP_ID_5560930,Human_RBP_ID_8778509,Human_RBP_ID_9255020,Human_RBP_ID_11873598,Human_RBP_ID_17683800,Human_RBP_ID_17812790,Human_RBP_ID_18199067,Human_RBP_ID_18206573,Human_RBP_ID_18433831,Human_RBP_ID_19701991,Human_RBP_ID_21917997,Human_RBP_ID_22492684,Human_RBP_ID_23268559,Human_RBP_ID_23305723,Human_RBP_ID_24529789,Human_RBP_ID_24539704,Human_RBP_ID_24947625,Human_RBP_ID_26423332,Human_RBP_ID_27154710,Human_RBP_ID_27420176 92746 RMVar_ID_92746 Human_SNP_ID_520330432 m1A Human chr12 - 128823475 128823475 128823475 CCGACGCCGCCGCCCGCTGCTGCTCACCGGCCACCTTCGCGGGGCTGGTGCTGGTGGGCCTGGGC CCGACGCCGCCGCCCGCTGCTGCTCACCGGCCGCCTTCGCGGGGCTGGTGCTGGTGGGCCTGGGC T C SLC15A4 Ensembl:ENSG00000139370 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:128823424..128823584 26863196 MeRIP-seq:(Medium) rs1403376844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5348963 Human_Splice_Rec_1444095,Human_Splice_Rec_1444109,Human_Splice_Rec_1444139,Human_Splice_Rec_1444147 RMVar_hsa_circ_161642,RMVar_hsa_circ_84074 92747 RMVar_ID_92747 Human_SNP_ID_520330690 m1A Human chr12 + 128823942 128823942 128823942 CCCGCTCGCCCGCACCGCCCCCAGAGCCCTCCATGCGACGCCGCCAGCTGCCTCGCCCCGCCGCC CCCGCTCGCCCGCACCGCCCCCAGAGCCCTCCGTGCGACGCCGCCAGCTGCCTCGCCCCGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:128823732..128823999 26863196 MeRIP-seq:(Medium) rs1326748289 Functional Loss SNV dbSNP153 33..33 33 - - - 92748 RMVar_ID_92748 Human_SNP_ID_493044981 m1A Human chr12 + 20368735 20368735 20368735 TGCCGGGGAGAATCGGCCGAGGAGAAAGAAAGAGTGATAGAAAAAGAGCTGCAGGAAGGAGGAGA TGCCGGGGAGAATCGGCCGAGGAGAAAGAAAGGGTGATAGAAAAAGAGCTGCAGGAAGGAGGAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:20368685..20368846 26863196 MeRIP-seq:(Medium) rs1021248297 Functional Loss SNV dbSNP153 33..33 33 - - - 92749 RMVar_ID_92749 Human_SNP_ID_493045167 m1A Human chr12 - 20369198 20369198 20369198 CGACCCACGCGCGCGCGCGCACACACACACACACACACACGCACGCACGCTCTTCCCAATTCCAC CGACCCACGCGCGCGCGCGCACACACACACACGCACACACGCACGCACGCTCTTCCCAATTCCAC T C AC129102.1 Ensembl:ENSG00000256879 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:20369148..20369317 26863196 MeRIP-seq:(Medium) rs1236606210 Functional Loss SNV dbSNP153 33..33 33 - - - 92750 RMVar_ID_92750 Human_SNP_ID_493045172 m1A Human chr12 - 20369208 20369208 20369208 GCCCCCGCCCCGACCCACGCGCGCGCGCGCACACACACACACACACACACGCACGCACGCTCTTC GCCCCCGCCCCGACCCACGCGCGCGCGCGCACGCACACACACACACACACGCACGCACGCTCTTC T C AC129102.1 Ensembl:ENSG00000256879 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:20369171..20369273 26863196 MeRIP-seq:(Medium) rs372956905 Functional Loss SNV dbSNP153 33..33 33 - - - 92751 RMVar_ID_92751 Human_SNP_ID_493045174 m1A Human chr12 - 20369210 20369210 20369210 ACGCCCCCGCCCCGACCCACGCGCGCGCGCGCACACACACACACACACACACGCACGCACGCTCT ACGCCCCCGCCCCGACCCACGCGCGCGCGCGCGCACACACACACACACACACGCACGCACGCTCT T C AC129102.1 Ensembl:ENSG00000256879 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:20369168..20369327;chr12:20369160..20369262 26863196 MeRIP-seq:(Medium) rs566929213 Functional Loss SNV dbSNP153 33..33 33 - - - 92752 RMVar_ID_92752 Human_SNP_ID_493063008 m1A Human chr12 - 20438848 20438848 20438848 GGTGGAGGCAGGAGAATCGCTTGAACCTGGGAAGTGGAGGTTGCAGTGAGCCAATATCATGCCAC GGTGGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAATATCATGCCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:20438801..20438954 26863196 MeRIP-seq:(Medium) rs1187243650 Functional Loss SNV dbSNP153 33..33 33 - - - 92753 RMVar_ID_92753 Human_SNP_ID_493069770 m1A Human chr12 + 20466983 20466983 20466983 CAGAGTTGAATTCAAATTTTTCAGAAATAAGCACATATTTTATTTGTTTTTTGAGACTTCTTTGT CAGAGTTGAATTCAAATTTTTCAGAAATAAGCCCATATTTTATTTGTTTTTTGAGACTTCTTTGT A C PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:20466973..20467195 26863196 MeRIP-seq:(Medium) rs943554796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2323248 92754 RMVar_ID_92754 Human_SNP_ID_493090499 m1A Human chr12 + 20551978 20551978 20551978 GGGTGTCCATCGGCCCCACGTGGCTGGCATCCATGGCCGGAGCAACGACGGAGCGTACTCCCTAG GGGTGTCCATCGGCCCCACGTGGCTGGCATCCGTGGCCGGAGCAACGACGGAGCGTACTCCCTAG A G PDE3A,AC112777.1 Ensembl:ENSG00000172572,Ensembl:ENSG00000256663 Protein coding,Pseudogene intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:20551936..20552076 26863196 MeRIP-seq:(Medium) rs547572880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36207,Human_RBP_ID_875810,Human_RBP_ID_4216422,Human_RBP_ID_8179592,Human_RBP_ID_8787594,Human_RBP_ID_12070961,Human_RBP_ID_17673084,Human_RBP_ID_18926384,Human_RBP_ID_21959585 92755 RMVar_ID_92755 Human_SNP_ID_493090500 m1A Human chr12 + 20551978 20551978 20551978 GGGTGTCCATCGGCCCCACGTGGCTGGCATCCATGGCCGGAGCAACGACGGAGCGTACTCCCTAG GGGTGTCCATCGGCCCCACGTGGCTGGCATCCTTGGCCGGAGCAACGACGGAGCGTACTCCCTAG A T PDE3A,AC112777.1 Ensembl:ENSG00000172572,Ensembl:ENSG00000256663 Protein coding,Pseudogene intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:20551936..20552076 26863196 MeRIP-seq:(Medium) rs547572880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36207,Human_RBP_ID_875810,Human_RBP_ID_4216422,Human_RBP_ID_8179592,Human_RBP_ID_8787594,Human_RBP_ID_12070961,Human_RBP_ID_17673084,Human_RBP_ID_18926384,Human_RBP_ID_21959585 92756 RMVar_ID_92756 Human_SNP_ID_493112669 m1A Human chr12 + 20643067 20643067 20643067 AGTGTATCAAGACGGAAGAGGGAGATGGGCGGACTCTGGGAAAGAGGTAGGGTGTACCATGTGCT AGTGTATCAAGACGGAAGAGGGAGATGGGCGGGCTCTGGGAAAGAGGTAGGGTGTACCATGTGCT A G PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:20643018..20643201 26863196 MeRIP-seq:(Medium) rs573336804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341985,RMVar_hsa_circ_102493,RMVar_hsa_circ_301529,RMVar_hsa_circ_155197,RMVar_hsa_circ_94384,RMVar_hsa_circ_40885,RMVar_hsa_circ_155201,RMVar_hsa_circ_375739,RMVar_hsa_circ_155204,RMVar_hsa_circ_155205,RMVar_hsa_circ_336724,RMVar_hsa_circ_155208,RMVar_hsa_circ_290380,RMVar_hsa_circ_155207,RMVar_hsa_circ_323587,RMVar_hsa_circ_374916,RMVar_hsa_circ_378687,RMVar_hsa_circ_155209 92757 RMVar_ID_92757 Human_SNP_ID_493337015 m1A Human chr12 - 21468957 21468957 21468957 CTTAAGATTTTTATCTAAGCGGTCAGTGTTGTATTGGAAAGATATATCTATAAATAAACTTTGAA CTTAAGATTTTTATCTAAGCGGTCAGTGTTGTGTTGGAAAGATATATCTATAAATAAACTTTGAA T C RECQL Ensembl:ENSG00000004700 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24465687 Human_miRNA_ID_925071,Human_miRNA_ID_2418440 GWAS_ID_12088,GWAS_ID_12089 RMVar_hsa_circ_155220,RMVar_hsa_circ_94484 92758 RMVar_ID_92758 Human_SNP_ID_493337092 m1A Human chr12 + 21469309 21469309 21469309 CAACTCTAGCCCACGGGTCTAATGCAGCCCAGAACAGCTTTGAATGCAGCCCAACACAAATCTGT CAACTCTAGCCCACGGGTCTAATGCAGCCCAGCACAGCTTTGAATGCAGCCCAACACAAATCTGT A C PYROXD1 Ensembl:ENSG00000121350 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:21469258..21469358 32194978 MeRIP-seq:(Medium) rs1332987997 Functional Loss SNV dbSNP153 33..33 33 - - - 92759 RMVar_ID_92759 Human_SNP_ID_493345197 m1A Human chr12 - 21501543 21501543 21501543 CGAGGCCTGGGTGCTTTGGTGTCGGAGATCCGAGAGTCGGAGATCGGAGAGTCGGACACAGGACA CGAGGCCTGGGTGCTTTGGTGTCGGAGATCCGCGAGTCGGAGATCGGAGAGTCGGACACAGGACA T G RECQL Ensembl:ENSG00000004700 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:21501462..21501600 26863196 MeRIP-seq:(Medium) rs1053837532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1469553,Human_RBP_ID_1792405,Human_RBP_ID_4216508,Human_RBP_ID_8787184,Human_RBP_ID_9278917,Human_RBP_ID_18623837 Human_Splice_Rec_1345601,Human_Splice_Rec_1345613,Human_Splice_Rec_1345625,Human_Splice_Rec_1345633,Human_Splice_Rec_1345645 92760 RMVar_ID_92760 Human_SNP_ID_493345330 m1A Human chr12 + 21501875 21501875 21501875 TCCCGGCTTCATTTCTCCCGACTCAGCTTCCCACCCTGGGCTTTCCGAGGTGCTGTCGCCGCTGT TCCCGGCTTCATTTCTCCCGACTCAGCTTCCCCCCCTGGGCTTTCCGAGGTGCTGTCGCCGCTGT A C GOLT1B Ensembl:ENSG00000111711 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:21501826..21501923 26863196 MeRIP-seq:(Medium) rs757650851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_416286,Human_RBP_ID_4246025,Human_RBP_ID_5437549,Human_RBP_ID_8372628,Human_RBP_ID_17356924,Human_RBP_ID_22039183,Human_RBP_ID_22910513,Human_RBP_ID_24364863 Human_Splice_Rec_1345653,Human_Splice_Rec_1345657,Human_Splice_Rec_1345665,Human_Splice_Rec_1345671,Human_Splice_Rec_1345673,Human_Splice_Rec_1345683,Human_Splice_Rec_1345689,Human_Splice_Rec_1345701,Human_Splice_Rec_1345711,Human_Splice_Rec_1345715 92761 RMVar_ID_92761 Human_SNP_ID_493345331 m1A Human chr12 + 21501875 21501875 21501875 TCCCGGCTTCATTTCTCCCGACTCAGCTTCCCACCCTGGGCTTTCCGAGGTGCTGTCGCCGCTGT TCCCGGCTTCATTTCTCCCGACTCAGCTTCCCGCCCTGGGCTTTCCGAGGTGCTGTCGCCGCTGT A G GOLT1B Ensembl:ENSG00000111711 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:21501826..21501923 26863196 MeRIP-seq:(Medium) rs757650851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_416286,Human_RBP_ID_4246025,Human_RBP_ID_5437549,Human_RBP_ID_8372628,Human_RBP_ID_17356924,Human_RBP_ID_22039183,Human_RBP_ID_22910513,Human_RBP_ID_24364863 Human_Splice_Rec_1345653,Human_Splice_Rec_1345657,Human_Splice_Rec_1345665,Human_Splice_Rec_1345671,Human_Splice_Rec_1345673,Human_Splice_Rec_1345683,Human_Splice_Rec_1345689,Human_Splice_Rec_1345701,Human_Splice_Rec_1345711,Human_Splice_Rec_1345715 92762 RMVar_ID_92762 Human_SNP_ID_493380195 m1A Human chr12 + 21641901 21641901 21641901 AAAAATAAAATTTGAAATAAAATGAAAAATTCAAAATGGCAAAACCAACATCACAAGTAATTATT AAAAATAAAATTTGAAATAAAATGAAAAATTCCAAATGGCAAAACCAACATCACAAGTAATTATT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:21641899..21642162 26863196 MeRIP-seq:(Medium) rs778657685 Functional Loss SNV dbSNP153 33..33 33 - - - 92763 RMVar_ID_92763 Human_SNP_ID_493380289 m1A Human chr12 + 21642118 21642118 21642118 AATCCACTTAGTTTCCAGGTAACATACGTAAGAATGTCCACTAAAAATTTTGGAAATAATATATG AATCCACTTAGTTTCCAGGTAACATACGTAAGTATGTCCACTAAAAATTTTGGAAATAATATATG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:21638351..21643606 32194978 MeRIP-seq:(Medium) rs771659456 Functional Loss SNV dbSNP153 33..33 33 - - - 92764 RMVar_ID_92764 Human_SNP_ID_493380744 m1A Human chr12 - 21643971 21643971 21643971 TCAAATTCATTATTCCTCAGATCGTCAAGTACAGTCCTGATTGCATCATAATTGTGGTTTCCAAC TCAAATTCATTATTCCTCAGATCGTCAAGTACCGTCCTGATTGCATCATAATTGTGGTTTCCAAC T G LDHB,AC010197.2 Ensembl:ENSG00000111716,Ensembl:ENSG00000285854 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:21643926..21654380 32194978 MeRIP-seq:(Medium) rs118203896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269523,Human_RBP_ID_416423,Human_RBP_ID_991302,Human_RBP_ID_1166203,Human_RBP_ID_1356960,Human_RBP_ID_1469601,Human_RBP_ID_1792447,Human_RBP_ID_2327943,Human_RBP_ID_3400881,Human_RBP_ID_3941475,Human_RBP_ID_4216606,Human_RBP_ID_5139826,Human_RBP_ID_5170403,Human_RBP_ID_6164760,Human_RBP_ID_8067202,Human_RBP_ID_8372685,Human_RBP_ID_8779824,Human_RBP_ID_9014751,Human_RBP_ID_9255109,Human_RBP_ID_9277665,Human_RBP_ID_11905702,Human_RBP_ID_17237571,Human_RBP_ID_17353459,Human_RBP_ID_17470085,Human_RBP_ID_17832255,Human_RBP_ID_18206299,Human_RBP_ID_18623880,Human_RBP_ID_22172862,Human_RBP_ID_22435806,Human_RBP_ID_22492980,Human_RBP_ID_22755846,Human_RBP_ID_22793792,Human_RBP_ID_23208010,Human_RBP_ID_23270030,Human_RBP_ID_23552163,Human_RBP_ID_26414872,Human_RBP_ID_26905110,Human_RBP_ID_27421012,Human_RBP_ID_27626629 Human_Splice_Rec_1345813,Human_Splice_Rec_1345883,Human_Splice_Rec_1345897,Human_Splice_Rec_1345911,Human_Splice_Rec_1345925 Clinvar_Rec_525 GWAS_ID_12090 RMVar_hsa_circ_5538,RMVar_hsa_circ_113832,RMVar_hsa_circ_104276,RMVar_hsa_circ_105309,RMVar_hsa_circ_94889,RMVar_hsa_circ_155230,RMVar_hsa_circ_155232,RMVar_hsa_circ_84785,RMVar_hsa_circ_155233,RMVar_hsa_circ_155231,RMVar_hsa_circ_155229,RMVar_hsa_circ_89741,RMVar_hsa_circ_14657,RMVar_hsa_circ_97579,RMVar_hsa_circ_155236,RMVar_hsa_circ_88276,RMVar_hsa_circ_155237,RMVar_hsa_circ_371434,RMVar_hsa_circ_155235,RMVar_hsa_circ_155238 92765 RMVar_ID_92765 Human_SNP_ID_493381675 m1A Human chr12 + 21647012 21647012 21647012 CCAAAACATCCACAAGAGCAAGTTCATCAGCCAGAGACTGTAAACGCAAAAACAGGCATTAGAAC CCAAAACATCCACAAGAGCAAGTTCATCAGCCGGAGACTGTAAACGCAAAAACAGGCATTAGAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:21646850..21647068 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 92766 RMVar_ID_92766 Human_SNP_ID_493383657 m1A Human chr12 - 21654527 21654527 21654527 TCAGCATTCTGGGAAAGGTACATTTCAAGAACACCATAGATGATAGAGAAGTTCAGCATGTATAC TCAGCATTCTGGGAAAGGTACATTTCAAGAACGCCATAGATGATAGAGAAGTTCAGCATGTATAC T C LDHB,AC010197.2 Ensembl:ENSG00000111716,Ensembl:ENSG00000285854 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:21654526..21656989 32194978 MeRIP-seq:(Medium) rs750596551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23552203,Human_RBP_ID_24957568 RMVar_hsa_circ_5538,RMVar_hsa_circ_113832,RMVar_hsa_circ_104276,RMVar_hsa_circ_105309,RMVar_hsa_circ_155232,RMVar_hsa_circ_155233,RMVar_hsa_circ_155231,RMVar_hsa_circ_89741,RMVar_hsa_circ_97579,RMVar_hsa_circ_155236,RMVar_hsa_circ_155235 92767 RMVar_ID_92767 Human_SNP_ID_493383698 m1A Human chr12 + 21654646 21654646 21654646 GAACTGTTGCCTCTTCTTCCGCAACTGGTGCAATGAGTTTTTCCTTAAGAGTTGCCATTTTGCAC GAACTGTTGCCTCTTCTTCCGCAACTGGTGCACTGAGTTTTTCCTTAAGAGTTGCCATTTTGCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:21654595..21654713 26863196 MeRIP-seq:(Medium) rs779501801 Functional Loss SNV dbSNP153 33..33 33 - - - 92768 RMVar_ID_92768 Human_SNP_ID_493383699 m1A Human chr12 + 21654646 21654646 21654646 GAACTGTTGCCTCTTCTTCCGCAACTGGTGCAATGAGTTTTTCCTTAAGAGTTGCCATTTTGCAC GAACTGTTGCCTCTTCTTCCGCAACTGGTGCAGTGAGTTTTTCCTTAAGAGTTGCCATTTTGCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:21654595..21654713 26863196 MeRIP-seq:(Medium) rs779501801 Functional Loss SNV dbSNP153 33..33 33 - - - 92769 RMVar_ID_92769 Human_SNP_ID_493384559 m1A Human chr12 + 21657801 21657800 21657801 GGAGACCTCTGTAACAGTCGTGCGGAGAAGACAAAGTCAGCTGCGTGCGTCTCCTCCGGCGCCGG GGAGACCTCTGTAACAGTCGTGCGGAGAAGAC_AAGTCAGCTGCGTGCGTCTCCTCCGGCGCCGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:21657659..21657850;chr12:21657701..21657850;chr12:21657686..21657850 26863196 MeRIP-seq:(Medium) rs752482900 Functional Loss DEL dbSNP153 33..33 33 - - - 92770 RMVar_ID_92770 Human_SNP_ID_493384560 m1A Human chr12 + 21657801 21657801 21657801 GGAGACCTCTGTAACAGTCGTGCGGAGAAGACAAAGTCAGCTGCGTGCGTCTCCTCCGGCGCCGG GGAGACCTCTGTAACAGTCGTGCGGAGAAGACGAAGTCAGCTGCGTGCGTCTCCTCCGGCGCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:21657659..21657850;chr12:21657701..21657850;chr12:21657686..21657850 26863196 MeRIP-seq:(Medium) rs1267641909 Functional Loss SNV dbSNP153 33..33 33 - - - 92771 RMVar_ID_92771 Human_SNP_ID_493478353 m1A Human chr12 + 22046301 22046301 22046301 ATGTGGAGAAGCTGGGGAGAAGGCGTGGGAGGAAGATGGACTCGGTGGAGAAGGGGGCCGCCACC ATGTGGAGAAGCTGGGGAGAAGGCGTGGGAGGTAGATGGACTCGGTGGAGAAGGGGGCCGCCACC A T CMAS Ensembl:ENSG00000111726 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:22046201..22046469 26863196 MeRIP-seq:(Medium) rs11554349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4216650,Human_RBP_ID_5314516,Human_RBP_ID_6164869,Human_RBP_ID_8940698,Human_RBP_ID_9352799,Human_RBP_ID_9366196,Human_RBP_ID_22436359 RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 92772 RMVar_ID_92772 Human_SNP_ID_493478363 m1A Human chr12 + 22046331 22046331 22046331 GGAAGATGGACTCGGTGGAGAAGGGGGCCGCCACCTCCGTCTCCAACCCGCGGGGGCGACCGTCC GGAAGATGGACTCGGTGGAGAAGGGGGCCGCCGCCTCCGTCTCCAACCCGCGGGGGCGACCGTCC A G CMAS Ensembl:ENSG00000111726 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:22046241..22046361 26863196 MeRIP-seq:(Medium) rs977836280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246026,Human_RBP_ID_5314516,Human_RBP_ID_8940698,Human_RBP_ID_9352799,Human_RBP_ID_22436359 RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 92773 RMVar_ID_92773 Human_SNP_ID_493478364 m1A Human chr12 + 22046331 22046331 22046331 GGAAGATGGACTCGGTGGAGAAGGGGGCCGCCACCTCCGTCTCCAACCCGCGGGGGCGACCGTCC GGAAGATGGACTCGGTGGAGAAGGGGGCCGCCTCCTCCGTCTCCAACCCGCGGGGGCGACCGTCC A T CMAS Ensembl:ENSG00000111726 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:22046241..22046361 26863196 MeRIP-seq:(Medium) rs977836280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246026,Human_RBP_ID_5314516,Human_RBP_ID_8940698,Human_RBP_ID_9352799,Human_RBP_ID_22436359 RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 92774 RMVar_ID_92774 Human_SNP_ID_493478381 m1A Human chr12 + 22046392 22046392 22046392 GTCCCGGGGCCGGCCGCCGAAGCTGCAGCGCAACTCTCGCGGCGGCCAGGGCCGAGGTGTGGAGA GTCCCGGGGCCGGCCGCCGAAGCTGCAGCGCAGCTCTCGCGGCGGCCAGGGCCGAGGTGTGGAGA A G CMAS Ensembl:ENSG00000111726 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:22046301..22046450 26863410 MeRIP-seq:(Medium) rs1351166826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6164871,Human_RBP_ID_8940698,Human_RBP_ID_22437634 RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 92775 RMVar_ID_92775 Human_SNP_ID_493478423 m1A Human chr12 + 22046487 22046487 22046487 CCCGGGGAGGCAGCAAAGGCATCCCCCTGAAGAACATTAAGCACCTGGCGGGGGTCCCGCTCATT CCCGGGGAGGCAGCAAAGGCATCCCCCTGAAGGACATTAAGCACCTGGCGGGGGTCCCGCTCATT A G CMAS Ensembl:ENSG00000111726 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1263984867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_416458,Human_RBP_ID_4216665,Human_RBP_ID_8372741,Human_RBP_ID_8786622,Human_RBP_ID_9278918,Human_RBP_ID_18623913 Human_Splice_Rec_1346233,Human_Splice_Rec_1346247,Human_Splice_Rec_1346259 RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 92776 RMVar_ID_92776 Human_SNP_ID_493597065 m1A Human chr12 - 22544173 22544173 22544173 GCAGACTCGTTTGTTTGTTTCTGCAGGAGCCCAAGAAGAGGCCGAAACCGAGACCATGCCAGGGA GCAGACTCGTTTGTTTGTTTCTGCAGGAGCCCGAGAAGAGGCCGAAACCGAGACCATGCCAGGGA T C C2CD5 Ensembl:ENSG00000111731 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:22544126..22544471 26863196 MeRIP-seq:(Medium) rs771149279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4216790,Human_RBP_ID_24958599 Human_Splice_Rec_1346388,Human_Splice_Rec_1346436,Human_Splice_Rec_1346488,Human_Splice_Rec_1346542,Human_Splice_Rec_1346644,Human_Splice_Rec_1346734 RMVar_hsa_circ_66939,RMVar_hsa_circ_64599,RMVar_hsa_circ_37492,RMVar_hsa_circ_331378,RMVar_hsa_circ_328599,RMVar_hsa_circ_359118,RMVar_hsa_circ_342116,RMVar_hsa_circ_57263,RMVar_hsa_circ_378022 92777 RMVar_ID_92777 Human_SNP_ID_493597070 m1A Human chr12 - 22544181 22544181 22544181 CGCTCGGCGCAGACTCGTTTGTTTGTTTCTGCAGGAGCCCAAGAAGAGGCCGAAACCGAGACCAT CGCTCGGCGCAGACTCGTTTGTTTGTTTCTGCGGGAGCCCAAGAAGAGGCCGAAACCGAGACCAT T C C2CD5 Ensembl:ENSG00000111731 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:22544137..22544303 26863196 MeRIP-seq:(Medium) rs1355314863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24958600 92778 RMVar_ID_92778 Human_SNP_ID_493597177 m1A Human chr12 + 22544360 22544360 22544360 GAGGAAGGGTGCTGTCCCGCGCGGGTGCTGAGACCTCATTCCGGAGAGGCGGCGGGAGGAAGGGC GAGGAAGGGTGCTGTCCCGCGCGGGTGCTGAGCCCTCATTCCGGAGAGGCGGCGGGAGGAAGGGC A C AC053513.1 Ensembl:ENSG00000250166 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:22544231..22544496 26863196 MeRIP-seq:(Medium) rs1356689699 Functional Loss SNV dbSNP153 33..33 33 - - - 92779 RMVar_ID_92779 Human_SNP_ID_494194825 m1A Human chr12 + 24907705 24907705 24907705 GAAGGTACTTTGTAATATCCTTCCCTGCCCTTAAGGTACTTTGTAATATTCTCCTCGCCCTTGAG GAAGGTACTTTGTAATATCCTTCCCTGCCCTTGAGGTACTTTGTAATATTCTCCTCGCCCTTGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:24907702..24907824 26863196 MeRIP-seq:(Medium) rs1044537823 Functional Loss SNV dbSNP153 33..33 33 - - - 92780 RMVar_ID_92780 Human_SNP_ID_494204870 m1A Human chr12 - 24948997 24948997 24948997 GCTCTGCAGCCGCAGACCCGGTCCACACGGCCAGGGGCTACGACCCTTGGGATCTGCCCTCCGCT GCTCTGCAGCCGCAGACCCGGTCCACACGGCCGGGGGCTACGACCCTTGGGATCTGCCCTCCGCT T C BCAT1 Ensembl:ENSG00000060982 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:24948951..24949210 26863196 MeRIP-seq:(Medium) rs920600938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4217200,Human_RBP_ID_5314870,Human_RBP_ID_9322455,Human_RBP_ID_9364741,Human_RBP_ID_17356944 Human_Splice_Rec_1347539,Human_Splice_Rec_1347579,Human_Splice_Rec_1347619,Human_Splice_Rec_1347661,Human_Splice_Rec_1347667 92781 RMVar_ID_92781 Human_SNP_ID_494281047 m1A Human chr12 + 25250849 25250849 25250849 CTCGCTCCCAGTCCGAAATGGCGGGGGCCGGGAGTACTGGCCGAGCCGCCGCCACCTTCGCCGCC CTCGCTCCCAGTCCGAAATGGCGGGGGCCGGGGGTACTGGCCGAGCCGCCGCCACCTTCGCCGCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:25250752..25250936 26863196 MeRIP-seq:(Medium) rs932064897 Functional Loss SNV dbSNP153 33..33 33 - - - 92782 RMVar_ID_92782 Human_SNP_ID_494281053 m1A Human chr12 - 25250874 25250860 25250875 AGGCAGCAGCGGCGGCGGCAGTGGCGGCGGCGAAGGTGGCGGCGGCTCGGCCAGTACTCCCGGCC AGGCAGCAGCGGCGGCGGCAGTGGCGGCGGC_______________TCGGCCAGTACTCCCGGCC AGCCGCCGCCACCTTC A KRAS Ensembl:ENSG00000133703 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:25250751..25250925 26863196 MeRIP-seq:(Medium) rs895194880 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_4217321 92783 RMVar_ID_92783 Human_SNP_ID_494281057 m1A Human chr12 - 25250873 25250862 25250874 GGCAGCAGCGGCGGCGGCAGTGGCGGCGGCGAAGGTGGCGGCGGCTCGGCCAGTACTCCCGGCCC GGCAGCAGCGGCGGCGGCAGTGGCGGCGGCG____________GCTCGGCCAGTACTCCCGGCCC CCGCCGCCACCTT C KRAS Ensembl:ENSG00000133703 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:25250708..25250925;chr12:25245332..25250936;chr12:25250691..25250904 26863196 MeRIP-seq:(Medium) rs948127681 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_4217321 92784 RMVar_ID_92784 Human_SNP_ID_494281057 m1A Human chr12 - 25250874 25250862 25250874 AGGCAGCAGCGGCGGCGGCAGTGGCGGCGGCGAAGGTGGCGGCGGCTCGGCCAGTACTCCCGGCC AGGCAGCAGCGGCGGCGGCAGTGGCGGCGGCG____________GCTCGGCCAGTACTCCCGGCC CCGCCGCCACCTT C KRAS Ensembl:ENSG00000133703 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:25250751..25250925 26863196 MeRIP-seq:(Medium) rs948127681 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_4217321 92785 RMVar_ID_92785 Human_SNP_ID_494312550 m1A Human chr12 + 25386156 25386156 25386156 TGCCGCCCCGCCACCTCACGCGCGCAGCGCTAACTGCAGCTCCGCAGCCACCGCCGTCGCCGCCG TGCCGCCCCGCCACCTCACGCGCGCAGCGCTACCTGCAGCTCCGCAGCCACCGCCGTCGCCGCCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:25386094..25386177 26863196 MeRIP-seq:(Medium) rs1380356632 Functional Loss SNV dbSNP153 33..33 33 - - - 92786 RMVar_ID_92786 Human_SNP_ID_494469255 m1A Human chr12 + 26027856 26027856 26027856 CTGAGCCAGAAATTCAATAATGTTAGCCTGAAAAAGAACAGCCCAGAAGATGACAGAGGGGAATG CTGAGCCAGAAATTCAATAATGTTAGCCTGAAGAAGAACAGCCCAGAAGATGACAGAGGGGAATG A G RASSF8 Ensembl:ENSG00000123094 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:26027852..26027993 26863196 MeRIP-seq:(Medium) rs1445539242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2329089 RMVar_hsa_circ_155344,RMVar_hsa_circ_347495,RMVar_hsa_circ_321711 92787 RMVar_ID_92787 Human_SNP_ID_494472968 m1A Human chr12 + 26043344 26043344 26043344 AGATGCTTGGGAGAGTGATAGATTGAGAGAACAGAAATGTCTTGGCATAAGGGTAGAGGGGAACT AGATGCTTGGGAGAGTGATAGATTGAGAGAACCGAAATGTCTTGGCATAAGGGTAGAGGGGAACT A C RASSF8 Ensembl:ENSG00000123094 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:26043342..26043451 26863196 MeRIP-seq:(Medium) rs1226783338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155344,RMVar_hsa_circ_347495,RMVar_hsa_circ_321711 92788 RMVar_ID_92788 Human_SNP_ID_494478774 m1A Human chr12 + 26067656 26067656 26067656 AGCAGTTCATCCAGCAGACAGGGACAAAAGTTACCGTTTTGCCAGCGGAGCCCATTGAAATAGAG AGCAGTTCATCCAGCAGACAGGGACAAAAGTTCCCGTTTTGCCAGCGGAGCCCATTGAAATAGAG A C RASSF8 Ensembl:ENSG00000123094 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:26067549..26067664 26863196 MeRIP-seq:(Medium) rs1427589953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8373137 Human_Splice_Rec_1348750,Human_Splice_Rec_1348751,Human_Splice_Rec_1348768,Human_Splice_Rec_1348769,Human_Splice_Rec_1348776,Human_Splice_Rec_1348777,Human_Splice_Rec_1348786,Human_Splice_Rec_1348787,Human_Splice_Rec_1348794,Human_Splice_Rec_1348795,Human_Splice_Rec_1348818,Human_Splice_Rec_1348819,Human_Splice_Rec_1348828,Human_Splice_Rec_1348829 RMVar_hsa_circ_155346,RMVar_hsa_circ_347495,RMVar_hsa_circ_273007,RMVar_hsa_circ_155348,RMVar_hsa_circ_278043,RMVar_hsa_circ_155349,RMVar_hsa_circ_291391,RMVar_hsa_circ_155350 92789 RMVar_ID_92789 Human_SNP_ID_494493166 m1A Human chr12 + 26124978 26124978 26124978 TCCACCGCGCTCGCACACACACACGCACACACACGCACACTCGCGCCGGCCCCACTGCGCTGGTA TCCACCGCGCTCGCACACACACACGCACACACGCGCACACTCGCGCCGGCCCCACTGCGCTGGTA A G SSPN Ensembl:ENSG00000123096 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:26124814..26125015 26863196 MeRIP-seq:(Medium) rs1435260190 Functional Loss SNV dbSNP153 33..33 33 - - - 92790 RMVar_ID_92790 Human_SNP_ID_494518263 m1A Human chr12 + 26234510 26234510 26234510 GGCAAATGTATTGACTCACAGTGGAAACATTCATTTGGATGAAGAATTAGTGGTTTAGCCTTTGA GGCAAATGTATTGACTCACAGTGGAAACATTCGTTTGGATGAAGAATTAGTGGTTTAGCCTTTGA A G SSPN Ensembl:ENSG00000123096 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7470 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12091,GWAS_ID_12092,GWAS_ID_12093 92791 RMVar_ID_92791 Human_SNP_ID_494518264 m1A Human chr12 + 26234510 26234510 26234511 GGCAAATGTATTGACTCACAGTGGAAACATTCATTTGGATGAAGAATTAGTGGTTTAGCCTTTGA GGCAAATGTATTGACTCACAGTGGAAACATTCGCTTGGATGAAGAATTAGTGGTTTAGCCTTTGA AT GC SSPN Ensembl:ENSG00000123096 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs386761340 Functional Loss MNV dbSNP153 33..34 33 - - - 92792 RMVar_ID_92792 Human_SNP_ID_494658668 m1A Human chr12 - 26833060 26833060 26833060 TGTTGGAGAGAAAACTTCAGAAAGGAACAGGAAACCTGCCGGGGAGGCGGCGGCGGCTGCGGCTT TGTTGGAGAGAAAACTTCAGAAAGGAACAGGATACCTGCCGGGGAGGCGGCGGCGGCTGCGGCTT T A ITPR2 Ensembl:ENSG00000123104 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:26833012..26833147 26863196 MeRIP-seq:(Medium) rs1040193407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877350,Human_RBP_ID_4246031,Human_RBP_ID_5521415,Human_RBP_ID_8229858,Human_RBP_ID_9366255,Human_RBP_ID_18417239,Human_RBP_ID_18975435,Human_RBP_ID_22040556,Human_RBP_ID_26323860 RMVar_hsa_circ_155417,RMVar_hsa_circ_110060 92793 RMVar_ID_92793 Human_SNP_ID_494677674 m1A Human chr12 - 26913533 26913533 26913533 AAGAGGAAGAACGAAAGAAACGAGGAAGAAAGAGGGAAGACAAAGAGGACAAGTCAGAGAAAGCA AAGAGGAAGAACGAAAGAAACGAGGAAGAAAGCGGGAAGACAAAGAGGACAAGTCAGAGAAAGCA T G INTS13 Ensembl:ENSG00000064102 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:26913482..26913576;chr12:26913451..26913626 26863196 MeRIP-seq:(Medium) rs1171061206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33263,Human_RBP_ID_24543052,Human_RBP_ID_26321263,Human_RBP_ID_27805325 Human_Splice_Rec_1349121,Human_Splice_Rec_1349153 RMVar_hsa_circ_54530,RMVar_hsa_circ_155419,RMVar_hsa_circ_112157,RMVar_hsa_circ_294155,RMVar_hsa_circ_360008,RMVar_hsa_circ_267096,RMVar_hsa_circ_363111,RMVar_hsa_circ_155420 92794 RMVar_ID_92794 Human_SNP_ID_494683815 m1A Human chr12 + 26938635 26938635 26938635 CGGATTAGGGGGGCGCGGAGTCTCTTCCCTTGAGTGCATAGGTCCCGGTTGGTAGAGGGTTTGAG CGGATTAGGGGGGCGCGGAGTCTCTTCCCTTGTGTGCATAGGTCCCGGTTGGTAGAGGGTTTGAG A T FGFR1OP2 Ensembl:ENSG00000111790 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:26938528..26938640 26863196 MeRIP-seq:(Medium) rs1201069827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_417254,Human_RBP_ID_4246561,Human_RBP_ID_6169225,Human_RBP_ID_9322458,Human_RBP_ID_9366256,Human_RBP_ID_11912488,Human_RBP_ID_18624414,Human_RBP_ID_22793862,Human_RBP_ID_23554099 Human_Splice_Rec_1349205,Human_Splice_Rec_1349217,Human_Splice_Rec_1349223,Human_Splice_Rec_1349229,Human_Splice_Rec_1349237 RMVar_hsa_circ_155430,RMVar_hsa_circ_79220 92795 RMVar_ID_92795 Human_SNP_ID_494702116 m1A Human chr12 - 27014213 27014213 27014213 CGAGGCTGCGGGGCCCCGGCGCGCACGCCCGCACCTCTCCCCAGCCCTGGCGTGGGCCCAGCCCG CGAGGCTGCGGGGCCCCGGCGCGCACGCCCGCTCCTCTCCCCAGCCCTGGCGTGGGCCCAGCCCG T A TM7SF3 Ensembl:ENSG00000064115 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:27014164..27014400 26863196 MeRIP-seq:(Medium) rs1408987520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246036,Human_RBP_ID_9323026,Human_RBP_ID_22436363,Human_RBP_ID_23554318 Human_miRNA_ID_2367355,Human_miRNA_ID_2684883,Human_miRNA_ID_3015152 RMVar_hsa_circ_378029,RMVar_hsa_circ_155445,RMVar_hsa_circ_155459,RMVar_hsa_circ_76192 92796 RMVar_ID_92796 Human_SNP_ID_494702132 m1A Human chr12 - 27014255 27014255 27014255 CGGGCGATGGCGCCCGATGCGGGCGCCCCGGGATAGCGTGGGCGAGGCTGCGGGGCCCCGGCGCG CGGGCGATGGCGCCCGATGCGGGCGCCCCGGGGTAGCGTGGGCGAGGCTGCGGGGCCCCGGCGCG T C TM7SF3 Ensembl:ENSG00000064115 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:27014101..27014377 26863196 MeRIP-seq:(Medium) rs1335751034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4246036,Human_RBP_ID_22436363 RMVar_hsa_circ_378029,RMVar_hsa_circ_155445,RMVar_hsa_circ_155459,RMVar_hsa_circ_76192 92797 RMVar_ID_92797 Human_SNP_ID_494757398 m1A Human chr12 + 27244299 27244299 27244299 GACGGGCGCCCGGCCGGCTGCGGTCCGTGCGGAGGCTGAGCCGGCCGCGGGCGCGACCGGAGGCA GACGGGCGCCCGGCCGGCTGCGGTCCGTGCGGGGGCTGAGCCGGCCGCGGGCGCGACCGGAGGCA A G STK38L Ensembl:ENSG00000211455 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:27244159..27244401 26863196 MeRIP-seq:(Medium) rs905965976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4218001,Human_RBP_ID_18417243 Human_Splice_Rec_1349457,Human_Splice_Rec_1349467,Human_Splice_Rec_1349477,Human_Splice_Rec_1349481,Human_Splice_Rec_1349483,Human_Splice_Rec_1349507,Human_Splice_Rec_1349515 Human_miRNA_ID_2269685 RMVar_hsa_circ_117233,RMVar_hsa_circ_155466 92798 RMVar_ID_92798 Human_SNP_ID_494785448 m1A Human chr12 + 27368277 27368277 27368277 TACTCTGCTGCCCATAGGTAAAGTGTTGAGAGAGGAGAACCAGTGCATTGCTCCTGTGGTTTCCA TACTCTGCTGCCCATAGGTAAAGTGTTGAGAGTGGAGAACCAGTGCATTGCTCCTGTGGTTTCCA A T ARNTL2 Ensembl:ENSG00000029153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:27332931..27368278;chr12:27332913..27368359;chr12:27332918..27368378 26863196 MeRIP-seq:(Medium) rs781272646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1349568,Human_Splice_Rec_1349598,Human_Splice_Rec_1349626,Human_Splice_Rec_1349652,Human_Splice_Rec_1349682,Human_Splice_Rec_1349710 RMVar_hsa_circ_25688,RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_295611,RMVar_hsa_circ_111023,RMVar_hsa_circ_337163,RMVar_hsa_circ_377191,RMVar_hsa_circ_155469,RMVar_hsa_circ_340443,RMVar_hsa_circ_304515,RMVar_hsa_circ_270475,RMVar_hsa_circ_280128,RMVar_hsa_circ_293365,RMVar_hsa_circ_279261,RMVar_hsa_circ_270206,RMVar_hsa_circ_270278,RMVar_hsa_circ_99156,RMVar_hsa_circ_155470,RMVar_hsa_circ_155474,RMVar_hsa_circ_155478,RMVar_hsa_circ_155480,RMVar_hsa_circ_155481,RMVar_hsa_circ_155482,RMVar_hsa_circ_155479,RMVar_hsa_circ_155476,RMVar_hsa_circ_155477,RMVar_hsa_circ_155475,RMVar_hsa_circ_155472,RMVar_hsa_circ_155473,RMVar_hsa_circ_155471 92799 RMVar_ID_92799 Human_SNP_ID_494788185 m1A Human chr12 + 27379428 27379428 27379428 GAATGAGATCTCAGGGTGAATAAAGAGTGAGGAGAGAGCGGTGCTAAGCAGGGAATCTTAGTGCA GAATGAGATCTCAGGGTGAATAAAGAGTGAGGGGAGAGCGGTGCTAAGCAGGGAATCTTAGTGCA A G ARNTL2 Ensembl:ENSG00000029153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:27379418..27379697 26863196 MeRIP-seq:(Medium) rs1021257124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25688,RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_295611,RMVar_hsa_circ_337163,RMVar_hsa_circ_377191,RMVar_hsa_circ_340443,RMVar_hsa_circ_304515,RMVar_hsa_circ_280128,RMVar_hsa_circ_279261,RMVar_hsa_circ_270206,RMVar_hsa_circ_155470,RMVar_hsa_circ_155474,RMVar_hsa_circ_155476,RMVar_hsa_circ_155475,RMVar_hsa_circ_155472,RMVar_hsa_circ_155473,RMVar_hsa_circ_155471,RMVar_hsa_circ_38572,RMVar_hsa_circ_335753,RMVar_hsa_circ_12200 92800 RMVar_ID_92800 Human_SNP_ID_494788194 m1A Human chr12 - 27379457 27379457 27379457 AGCTCTTACTTGATCCTTAAATACTGGTGTGCACTAAGATTCCCTGCTTAGCACCGCTCTCTCCT AGCTCTTACTTGATCCTTAAATACTGGTGTGCCCTAAGATTCCCTGCTTAGCACCGCTCTCTCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:27379452..27379606 26863196 MeRIP-seq:(Medium) rs954290390 Functional Loss SNV dbSNP153 33..33 33 - - - 92801 RMVar_ID_92801 Human_SNP_ID_494823762 m1A Human chr12 + 27533757 27533756 27533758 GAGCTCCCCGAACAAGAGTATGTAGAGTAAAAAGAGAAGCAAGCATACAGTCTTCAGGGGACTCC GAGCTCCCCGAACAAGAGTATGTAGAGTAAAA__AGAAGCAAGCATACAGTCTTCAGGGGACTCC AAG A PPFIBP1 Ensembl:ENSG00000110841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:27533750..27533815 26863196 MeRIP-seq:(Medium) rs1343371982 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466 92802 RMVar_ID_92802 Human_SNP_ID_494864387 m1A Human chr12 - 27710897 27710895 27710897 GCCGAGTAGACGGCAGTGGAGAATGCACGCAGAGTCCTTGCCCTCGACTGCAGAGACAGCCATGC GCCGAGTAGACGGCAGTGGAGAATGCACGCAG__TCCTTGCCCTCGACTGCAGAGACAGCCATGC ACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:27710847..27710952 26863196 MeRIP-seq:(Medium) rs1566045131 Functional Loss DEL dbSNP153 33..34 33 - - - 92803 RMVar_ID_92803 Human_SNP_ID_494864389 m1A Human chr12 - 27710897 27710897 27710897 GCCGAGTAGACGGCAGTGGAGAATGCACGCAGAGTCCTTGCCCTCGACTGCAGAGACAGCCATGC GCCGAGTAGACGGCAGTGGAGAATGCACGCAGGGTCCTTGCCCTCGACTGCAGAGACAGCCATGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:27710847..27710952 26863196 MeRIP-seq:(Medium) rs748655948 Functional Loss SNV dbSNP153 33..33 33 - - - 92804 RMVar_ID_92804 Human_SNP_ID_494870464 m1A Human chr12 + 27737585 27737584 27737586 GGCAGAATTACGATTATGCAGTGTATCTACTAACAGTGTTATACCATGAGTCTTGGGTAAGTGTG GGCAGAATTACGATTATGCAGTGTATCTACTA__AGTGTTATACCATGAGTCTTGGGTAAGTGTG AAC A MRPS35 Ensembl:ENSG00000061794 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:27735553..27755355 32194978 MeRIP-seq:(Medium) rs754400770 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_417611,Human_RBP_ID_9344227,Human_RBP_ID_23554699 Human_Splice_Rec_1350238,Human_Splice_Rec_1350239,Human_Splice_Rec_1350250,Human_Splice_Rec_1350251,Human_Splice_Rec_1350268 Human_miRNA_ID_2060127,Human_miRNA_ID_2185523 RMVar_hsa_circ_316814,RMVar_hsa_circ_155515,RMVar_hsa_circ_88661,RMVar_hsa_circ_39378,RMVar_hsa_circ_155516,RMVar_hsa_circ_358058,RMVar_hsa_circ_155519,RMVar_hsa_circ_304922 92805 RMVar_ID_92805 Human_SNP_ID_494874570 m1A Human chr12 + 27755670 27755670 27755670 AGACTAGGAGGTCTCTGATTTCTTCTTGGTCTAAAGTGTTTTGATTTTATTTCTACATAATAGCT AGACTAGGAGGTCTCTGATTTCTTCTTGGTCTGAAGTGTTTTGATTTTATTTCTACATAATAGCT A G MRPS35 Ensembl:ENSG00000061794 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3751233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36369,Human_RBP_ID_417624,Human_RBP_ID_2330107,Human_RBP_ID_3402229,Human_RBP_ID_6170651,Human_RBP_ID_8373428,Human_RBP_ID_11915194,Human_RBP_ID_23208017,Human_RBP_ID_24465888,Human_RBP_ID_26423520 Human_miRNA_ID_851262 GWAS_ID_12094,GWAS_ID_12095,GWAS_ID_12096,GWAS_ID_12097,GWAS_ID_12098,GWAS_ID_12099,GWAS_ID_12100,GWAS_ID_12101,GWAS_ID_12102,GWAS_ID_12103,GWAS_ID_12104,GWAS_ID_12105,GWAS_ID_12106,GWAS_ID_12107,GWAS_ID_12108,GWAS_ID_12109,GWAS_ID_12110,GWAS_ID_12111,GWAS_ID_12112,GWAS_ID_12113,GWAS_ID_12114 92806 RMVar_ID_92806 Human_SNP_ID_494880454 m1A Human chr12 + 27780279 27780272 27780279 CGCCCGGAACCGGCGCGCGCGTAGGGGCTGGGAGGCCGGCGCGCAGATCTGGCGGTGAGCGCTGC CGCCCGGAACCGGCGCGCGCGTAGGG_______GGCCGGCGCGCAGATCTGGCGGTGAGCGCTGC GGCTGGGA G KLHL42 Ensembl:ENSG00000087448 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:27780239..27780444 26863196 MeRIP-seq:(Medium) rs1215519228 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_22493032 92807 RMVar_ID_92807 Human_SNP_ID_494880459 m1A Human chr12 + 27780279 27780279 27780279 CGCCCGGAACCGGCGCGCGCGTAGGGGCTGGGAGGCCGGCGCGCAGATCTGGCGGTGAGCGCTGC CGCCCGGAACCGGCGCGCGCGTAGGGGCTGGGGGGCCGGCGCGCAGATCTGGCGGTGAGCGCTGC A G KLHL42 Ensembl:ENSG00000087448 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:27780239..27780444 26863196 MeRIP-seq:(Medium) rs1253532991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22493032 92808 RMVar_ID_92808 Human_SNP_ID_494974011 m1A Human chr12 + 28190590 28190590 28190590 GGGGTCTGTGTGCTGGGGGTGGCTCACCGGGCAGCGTGGGTGAGCGGCGCAGCGGCGGCAGCGGA GGGGTCTGTGTGCTGGGGGTGGCTCACCGGGCGGCGTGGGTGAGCGGCGCAGCGGCGGCAGCGGA A G CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr12:28190476..28190667;chr12:28190451..28190650;chr12:28190540..28190689 26863196,32194978 MeRIP-seq:(Medium) rs1265019468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065451,Human_RBP_ID_4246569,Human_RBP_ID_18417643,Human_RBP_ID_26322738,Human_RBP_ID_26777264 Human_Splice_Rec_1350397,Human_Splice_Rec_1350419,Human_Splice_Rec_1350439,Human_Splice_Rec_1350445,Human_Splice_Rec_1350475 92809 RMVar_ID_92809 Human_SNP_ID_495014005 m1A Human chr12 + 28364625 28364625 28364625 GCCTAATATATTTGCAGATTCCATAACCATGGATGAGAAATGTTTGGGGAAGAAAAGCAATAAAA GCCTAATATATTTGCAGATTCCATAACCATGGGTGAGAAATGTTTGGGGAAGAAAAGCAATAAAA A G CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:28364612..28364766 32194978 MeRIP-seq:(Medium) rs948415568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6171654,Human_RBP_ID_9679227 RMVar_hsa_circ_4996,RMVar_hsa_circ_355108,RMVar_hsa_circ_68151,RMVar_hsa_circ_309605,RMVar_hsa_circ_271409,RMVar_hsa_circ_331879,RMVar_hsa_circ_366179,RMVar_hsa_circ_300770,RMVar_hsa_circ_55096,RMVar_hsa_circ_277465,RMVar_hsa_circ_281288,RMVar_hsa_circ_293054,RMVar_hsa_circ_278642,RMVar_hsa_circ_277446,RMVar_hsa_circ_95347,RMVar_hsa_circ_55846,RMVar_hsa_circ_155538,RMVar_hsa_circ_155539,RMVar_hsa_circ_110591,RMVar_hsa_circ_5211,RMVar_hsa_circ_273367,RMVar_hsa_circ_155543,RMVar_hsa_circ_73696,RMVar_hsa_circ_155544 92810 RMVar_ID_92810 Human_SNP_ID_495014006 m1A Human chr12 + 28364625 28364625 28364625 GCCTAATATATTTGCAGATTCCATAACCATGGATGAGAAATGTTTGGGGAAGAAAAGCAATAAAA GCCTAATATATTTGCAGATTCCATAACCATGGTTGAGAAATGTTTGGGGAAGAAAAGCAATAAAA A T CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:28364612..28364766 32194978 MeRIP-seq:(Medium) rs948415568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6171654,Human_RBP_ID_9679227 RMVar_hsa_circ_4996,RMVar_hsa_circ_355108,RMVar_hsa_circ_68151,RMVar_hsa_circ_309605,RMVar_hsa_circ_271409,RMVar_hsa_circ_331879,RMVar_hsa_circ_366179,RMVar_hsa_circ_300770,RMVar_hsa_circ_55096,RMVar_hsa_circ_277465,RMVar_hsa_circ_281288,RMVar_hsa_circ_293054,RMVar_hsa_circ_278642,RMVar_hsa_circ_277446,RMVar_hsa_circ_95347,RMVar_hsa_circ_55846,RMVar_hsa_circ_155538,RMVar_hsa_circ_155539,RMVar_hsa_circ_110591,RMVar_hsa_circ_5211,RMVar_hsa_circ_273367,RMVar_hsa_circ_155543,RMVar_hsa_circ_73696,RMVar_hsa_circ_155544 92811 RMVar_ID_92811 Human_SNP_ID_495033952 m1A Human chr12 + 28452582 28452581 28452583 CATGCTGAAGAAAGGGAATTATGGAAGACAGAACATGCAAAAGATCAAGAAAAAGTATCTCAGGA CATGCTGAAGAAAGGGAATTATGGAAGACAGA__ATGCAAAAGATCAAGAAAAAGTATCTCAGGA AAC A CCDC91 Ensembl:ENSG00000123106 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:28452536..28452685 26863196 MeRIP-seq:(Medium) rs1565996909 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1479522,Human_RBP_ID_23555118,Human_RBP_ID_26321264,Human_RBP_ID_27805330 Human_Splice_Rec_1350367,Human_Splice_Rec_1350393,Human_Splice_Rec_1350415,Human_Splice_Rec_1350471,Human_Splice_Rec_1350517,Human_Splice_Rec_1350557,Human_Splice_Rec_1350579,Human_Splice_Rec_1350599,Human_Splice_Rec_1350601 Human_miRNA_ID_1309193,Human_miRNA_ID_1688924 RMVar_hsa_circ_355108,RMVar_hsa_circ_68151,RMVar_hsa_circ_331879,RMVar_hsa_circ_366179,RMVar_hsa_circ_55096,RMVar_hsa_circ_293054,RMVar_hsa_circ_278642,RMVar_hsa_circ_95347,RMVar_hsa_circ_155538,RMVar_hsa_circ_110591,RMVar_hsa_circ_5211,RMVar_hsa_circ_155543,RMVar_hsa_circ_287767,RMVar_hsa_circ_273786,RMVar_hsa_circ_155545,RMVar_hsa_circ_155546,RMVar_hsa_circ_282674,RMVar_hsa_circ_61899,RMVar_hsa_circ_307642,RMVar_hsa_circ_155547 92812 RMVar_ID_92812 Human_SNP_ID_495251875 m1A Human chr12 + 29349086 29349086 29349086 CCAACAATAATTATTAAATACTTACGATCTATAGCAATTTTTTCAGTTCCATCTAAAGGATTAAT CCAACAATAATTATTAAATACTTACGATCTATGGCAATTTTTTCAGTTCCATCTAAAGGATTAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:29349083..29350018 32194978 MeRIP-seq:(Medium) rs1424272322 Functional Loss SNV dbSNP153 33..33 33 - - - 92813 RMVar_ID_92813 Human_SNP_ID_495257062 m1A Human chr12 + 29371638 29371638 29371638 AAGTTTTTTTCCGATTCAGTCGCCTCATCTTCAGGAAAACCTTCCTCTTCCTTCATATAGTCATG AAGTTTTTTTCCGATTCAGTCGCCTCATCTTCGGGAAAACCTTCCTCTTCCTTCATATAGTCATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:29371588..29371678 26863196 MeRIP-seq:(Medium) rs775062759 Functional Loss SNV dbSNP153 33..33 33 - - - 92814 RMVar_ID_92814 Human_SNP_ID_495359100 m1A Human chr12 + 29783541 29783541 29783541 CTTGCCCCAGAAGTCGTTGGTGAAGATGCCCCAGCGGAGCGGGGCGCCGGGCCGCACGTCGGGGT CTTGCCCCAGAAGTCGTTGGTGAAGATGCCCCCGCGGAGCGGGGCGCCGGGCCGCACGTCGGGGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:29783501..29783899 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 92815 RMVar_ID_92815 Human_SNP_ID_495359101 m1A Human chr12 + 29783541 29783541 29783541 CTTGCCCCAGAAGTCGTTGGTGAAGATGCCCCAGCGGAGCGGGGCGCCGGGCCGCACGTCGGGGT CTTGCCCCAGAAGTCGTTGGTGAAGATGCCCCTGCGGAGCGGGGCGCCGGGCCGCACGTCGGGGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:29783501..29783899 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 92816 RMVar_ID_92816 Human_SNP_ID_495359275 m1A Human chr12 + 29783876 29783876 29783876 GGGGGGCTCGGGCATGGTGCTGCGGCAGCTGGACCCGCCGCGAGCTCCCCGCGCTCCGCCGCCGC GGGGGGCTCGGGCATGGTGCTGCGGCAGCTGGCCCCGCCGCGAGCTCCCCGCGCTCCGCCGCCGC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:29783807..29783889 26863410 MeRIP-seq:(Medium) rs1032477973 Functional Loss SNV dbSNP153 33..33 33 - - - 92817 RMVar_ID_92817 Human_SNP_ID_605073127 m1A Human chr16 - 61055932 61055932 61055932 TAAAGAGTTCTATAGATTGAGAAGCTATCTGCAGTGGAGCCGCCACCAAAATGCAGATTTTCGTG TAAAGAGTTCTATAGATTGAGAAGCTATCTGCTGTGGAGCCGCCACCAAAATGCAGATTTTCGTG T A RPS27AP16 Ensembl:ENSG00000224631 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112657530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26811438 92818 RMVar_ID_92818 Human_SNP_ID_605073128 m1A Human chr16 - 61055932 61055932 61055932 TAAAGAGTTCTATAGATTGAGAAGCTATCTGCAGTGGAGCCGCCACCAAAATGCAGATTTTCGTG TAAAGAGTTCTATAGATTGAGAAGCTATCTGCGGTGGAGCCGCCACCAAAATGCAGATTTTCGTG T C RPS27AP16 Ensembl:ENSG00000224631 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112657530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26811438 92819 RMVar_ID_92819 Human_SNP_ID_605073129 m1A Human chr16 - 61055932 61055932 61055932 TAAAGAGTTCTATAGATTGAGAAGCTATCTGCAGTGGAGCCGCCACCAAAATGCAGATTTTCGTG TAAAGAGTTCTATAGATTGAGAAGCTATCTGCCGTGGAGCCGCCACCAAAATGCAGATTTTCGTG T G RPS27AP16 Ensembl:ENSG00000224631 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112657530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26811438 92820 RMVar_ID_92820 Human_SNP_ID_606417424 m1A Human chr16 + 66427104 66427104 66427104 CCGGTGACGGTGGCGTGGGCGGCGGCGCGGGGACGACGGGCGGCCGGGCGGGGCTGCGGCAGGGC CCGGTGACGGTGGCGTGGGCGGCGGCGCGGGGTCGACGGGCGGCCGGGCGGGGCTGCGGCAGGGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66427020..66427142 26863196 MeRIP-seq:(Medium) rs1341021514 Functional Loss SNV dbSNP153 33..33 33 - - - 92821 RMVar_ID_92821 Human_SNP_ID_606433947 m1A Human chr16 + 66495522 66495522 66495522 TTCCTTCTTTCCTTCCTTCCCTCCATCCAACCATCCATCCATCCCTGCCTCCCACCTCCCTCCTG TTCCTTCTTTCCTTCCTTCCCTCCATCCAACCGTCCATCCATCCCTGCCTCCCACCTCCCTCCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:66495471..66495542 26863196 MeRIP-seq:(Medium) rs1346648729 Functional Loss SNV dbSNP153 33..33 33 - - - 92822 RMVar_ID_92822 Human_SNP_ID_606442501 m1A Human chr16 - 66529845 66529845 66529845 AGGAAAGAGAGGATGGAAGAATGGAAAGGAAGATGGATGGGCAGAGGATGGATGGACAGAGGGAC AGGAAAGAGAGGATGGAAGAATGGAAAGGAAGTTGGATGGGCAGAGGATGGATGGACAGAGGGAC T A TK2 Ensembl:ENSG00000166548 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66529834..66529928 26863196 MeRIP-seq:(Medium) rs981135230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33042,RMVar_hsa_circ_274881,RMVar_hsa_circ_11219,RMVar_hsa_circ_21481,RMVar_hsa_circ_178941,RMVar_hsa_circ_28034,RMVar_hsa_circ_365686,RMVar_hsa_circ_39925,RMVar_hsa_circ_70458,RMVar_hsa_circ_307120,RMVar_hsa_circ_285364,RMVar_hsa_circ_178943,RMVar_hsa_circ_178944 92823 RMVar_ID_92823 Human_SNP_ID_606447508 m1A Human chr16 + 66550045 66550045 66550045 AGCAGCGCAGCGCCCGGGCGGCCCAGCCCCGCAGCGGCCACAGCAGCATAGCCGGGCGAGCGGAT AGCAGCGCAGCGCCCGGGCGGCCCAGCCCCGCGGCGGCCACAGCAGCATAGCCGGGCGAGCGGAT A G AC010542.4 Ensembl:ENSG00000261519 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66549995..66550088 26863196 MeRIP-seq:(Medium) rs779367525 Functional Loss SNV dbSNP153 33..33 33 - - - 92824 RMVar_ID_92824 Human_SNP_ID_606448324 m1A Human chr16 - 66552644 66552644 66552644 TTCTCAGCTGGCTGCCTGAGTAGGTTCTGCGAAGCGATAGCAACCGCCACCGCGGCGGAGCACCG TTCTCAGCTGGCTGCCTGAGTAGGTTCTGCGAGGCGATAGCAACCGCCACCGCGGCGGAGCACCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:66552593..66552775 26863196 MeRIP-seq:(Medium) rs969377706 Functional Loss SNV dbSNP153 33..33 33 - - - 92825 RMVar_ID_92825 Human_SNP_ID_606448325 m1A Human chr16 - 66552645 66552645 66552645 CTTCTCAGCTGGCTGCCTGAGTAGGTTCTGCGAAGCGATAGCAACCGCCACCGCGGCGGAGCACC CTTCTCAGCTGGCTGCCTGAGTAGGTTCTGCGGAGCGATAGCAACCGCCACCGCGGCGGAGCACC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:66552601..66552732 26863196 MeRIP-seq:(Medium) rs1373108573 Functional Loss SNV dbSNP153 33..33 33 - - - 92826 RMVar_ID_92826 Human_SNP_ID_606448348 m1A Human chr16 - 66552694 66552694 66552694 ACGTTATCCATCGCGTCTGCAGACCCAGCAGCAGCACTTTCCCTCAACTCTTCTCAGCTGGCTGC ACGTTATCCATCGCGTCTGCAGACCCAGCAGCTGCACTTTCCCTCAACTCTTCTCAGCTGGCTGC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:66552609..66552722 26863196 MeRIP-seq:(Medium) rs776601179 Functional Loss SNV dbSNP153 33..33 33 - - - 92827 RMVar_ID_92827 Human_SNP_ID_606449909 m1A Human chr16 + 66559994 66559993 66559995 CAGAAACTTTAAATGCACCCAGGAAGCAACACAGAGAATATAGGTGCTATGAGAGATATACACCT CAGAAACTTTAAATGCACCCAGGAAGCAACAC__AGAATATAGGTGCTATGAGAGATATACACCT CAG C CKLF-CMTM1,CKLF Ensembl:ENSG00000254788,Ensembl:ENSG00000217555 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:66559991..66560427 26863196 MeRIP-seq:(Medium) rs1171975142 Functional Loss DEL dbSNP153 33..34 33 - - - 92828 RMVar_ID_92828 Human_SNP_ID_606449920 m1A Human chr16 + 66560066 66560066 66560066 CGTGGATGCAACCCAGCAAGGGAAAGGGACCAAGTCACAGTAGGCTGTGAAGAAAAAGTGCCCAA CGTGGATGCAACCCAGCAAGGGAAAGGGACCAGGTCACAGTAGGCTGTGAAGAAAAAGTGCCCAA A G CKLF-CMTM1,CKLF Ensembl:ENSG00000254788,Ensembl:ENSG00000217555 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66560062..66560421 26863196 MeRIP-seq:(Medium) rs1267150923 Functional Loss SNV dbSNP153 33..33 33 - - - 92829 RMVar_ID_92829 Human_SNP_ID_606450645 m1A Human chr16 + 66563146 66563146 66563146 GTTTTTAGGATATTATCAACTCACTGGTAACAACAGTATTCATGCTCATCGTATCTGTGTTGGCA GTTTTTAGGATATTATCAACTCACTGGTAACAGCAGTATTCATGCTCATCGTATCTGTGTTGGCA A G CKLF-CMTM1,CKLF Ensembl:ENSG00000254788,Ensembl:ENSG00000217555 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:66563143..66566107 32194978 MeRIP-seq:(Medium) rs749672003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476783,Human_RBP_ID_1178616,Human_RBP_ID_1520269,Human_RBP_ID_1844451,Human_RBP_ID_17370332,Human_RBP_ID_17879017,Human_RBP_ID_22759860,Human_RBP_ID_26810437 Human_Splice_Rec_1723450,Human_Splice_Rec_1723451,Human_Splice_Rec_1723454,Human_Splice_Rec_1723455,Human_Splice_Rec_1723468,Human_Splice_Rec_1723469,Human_Splice_Rec_1723474,Human_Splice_Rec_1723475,Human_Splice_Rec_1723478,Human_Splice_Rec_1723479,Human_Splice_Rec_1723482,Human_Splice_Rec_1723483,Human_Splice_Rec_1723490,Human_Splice_Rec_1723491,Human_Splice_Rec_1723494,Human_Splice_Rec_1723495,Human_Splice_Rec_1723505 92830 RMVar_ID_92830 Human_SNP_ID_606454342 m1A Human chr16 - 66579042 66579042 66579042 ATGCGAGCTCGGGGGTGGGCTCGGAGGCAGCGATTCGACAGACACGTGCATCTGCTAGGGCGCCG ATGCGAGCTCGGGGGTGGGCTCGGAGGCAGCGCTTCGACAGACACGTGCATCTGCTAGGGCGCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66578994..66579083 26863196 MeRIP-seq:(Medium) rs1215249427 Functional Loss SNV dbSNP153 33..33 33 - - - 92831 RMVar_ID_92831 Human_SNP_ID_606454441 m1A Human chr16 - 66579362 66579362 66579362 GGATCCTCCCACCCTCCACGCGCCGGCCCCCGACGGGCCCCAACTCCGTTCCCAACCCGCCGGTC GGATCCTCCCACCCTCCACGCGCCGGCCCCCGTCGGGCCCCAACTCCGTTCCCAACCCGCCGGTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:66579322..66579455 26863196 MeRIP-seq:(Medium) rs1428830604 Functional Loss SNV dbSNP153 33..33 33 - - - 92832 RMVar_ID_92832 Human_SNP_ID_606462919 m1A Human chr16 + 66613297 66613297 66613297 TCTGGGGGTGAGATGACCATTCTGGGTCTAAGACTGTTTCAAAGAAGAGCTCATAGACTGACTGG TCTGGGGGTGAGATGACCATTCTGGGTCTAAGTCTGTTTCAAAGAAGAGCTCATAGACTGACTGG A T CMTM3 Ensembl:ENSG00000140931 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:66613249..66613349 32194978 MeRIP-seq:(Medium) rs1393343254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1520280,Human_RBP_ID_1844459,Human_RBP_ID_8808868,Human_RBP_ID_18286368,Human_RBP_ID_26442292 Human_miRNA_ID_226942,Human_miRNA_ID_589795,Human_miRNA_ID_2026607,Human_miRNA_ID_2216248,Human_miRNA_ID_2894589 RMVar_hsa_circ_111499,RMVar_hsa_circ_178950 92833 RMVar_ID_92833 Human_SNP_ID_606464846 m1A Human chr16 + 66622068 66622068 66622068 GGAGGAGGATCCAGGCAGGTCCTCACGTGTCCAGGCGCTGGATCTCAGGGCGACTGTCCACATCC GGAGGAGGATCCAGGCAGGTCCTCACGTGTCCGGGCGCTGGATCTCAGGGCGACTGTCCACATCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:66622019..66622169 32194978 MeRIP-seq:(Medium) rs1458791918 Functional Loss SNV dbSNP153 33..33 33 - - - 92834 RMVar_ID_92834 Human_SNP_ID_606468912 m1A Human chr16 - 66638051 66638051 66638051 GGGGAGGAGGTGGCGGCATCATCAAGTGGAGCATTGGAAAGCATGAGTAGGACTTTCAGCAGGTG GGGGAGGAGGTGGCGGCATCATCAAGTGGAGCTTTGGAAAGCATGAGTAGGACTTTCAGCAGGTG T A CMTM4 Ensembl:ENSG00000183723 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66638048..66638131 26863196 MeRIP-seq:(Medium) rs748297068 Functional Loss SNV dbSNP153 33..33 33 - - - 92835 RMVar_ID_92835 Human_SNP_ID_606483013 m1A Human chr16 + 66696186 66696185 66696187 TGGCCGAAGGCGGGGTCCCCAGAGAAGGCTGCAGAGTGGTCCCGGGACCCCACGAGGGAGAGGGG TGGCCGAAGGCGGGGTCCCCAGAGAAGGCTGC__AGTGGTCCCGGGACCCCACGAGGGAGAGGGG CAG C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:66696180..66696307 26863196 MeRIP-seq:(Medium) rs1189780184 Functional Loss DEL dbSNP153 33..34 33 - - - 92836 RMVar_ID_92836 Human_SNP_ID_606483120 m1A Human chr16 - 66696512 66696512 66696512 GCCCGGGCCGGGCGGCAGCATGCGGAGCGGCGAGGAGCTGGACGGCTTCGAGGGCGAGGCCTCGA GCCCGGGCCGGGCGGCAGCATGCGGAGCGGCGTGGAGCTGGACGGCTTCGAGGGCGAGGCCTCGA T A CMTM4 Ensembl:ENSG00000183723 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:66696388..66696599 26863196 MeRIP-seq:(Medium) rs1370706689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393164,Human_RBP_ID_5237545 Human_Splice_Rec_1723751 92837 RMVar_ID_92837 Human_SNP_ID_606483176 m1A Human chr16 + 66696634 66696624 66696634 ATCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGACTGACTGCCCGCGGCCCGCCCGCCGCCGCCGC ATCGCCGCCGCCGCCGCCGCCGC__________CTGACTGCCCGCGGCCCGCCCGCCGCCGCCGC CCGCCGCCCGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr16:66696542..66696653;chr16:66696290..66696740 26863410,26863196 MeRIP-seq:(Medium) rs1199690822 Functional Loss DEL dbSNP153 24..33 33 - - - 92838 RMVar_ID_92838 Human_SNP_ID_606483209 m1A Human chr16 - 66696698 66696698 66696698 CGAGGCGGCGGGAGCCGAGCCCGAGCGGACCGAGCCGCAGCCGCAGCCGGGCGGCGGGCGAGAGG CGAGGCGGCGGGAGCCGAGCCCGAGCGGACCGTGCCGCAGCCGCAGCCGGGCGGCGGGCGAGAGG T A CMTM4 Ensembl:ENSG00000183723 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:66696611..66696711 26863410 MeRIP-seq:(Medium) rs1299346910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4376590 92839 RMVar_ID_92839 Human_SNP_ID_606489650 m1A Human chr16 - 66722487 66722487 66722487 TGGAAATAAGAGTTTCAGGTGTCTCCCCACCTAGGGCAAATTCATGCACATTGTCATGTTATACC TGGAAATAAGAGTTTCAGGTGTCTCCCCACCTGGGGCAAATTCATGCACATTGTCATGTTATACC T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:66722438..66722638 32194978 MeRIP-seq:(Medium) rs1040519435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477060,Human_RBP_ID_761331,Human_RBP_ID_1178630,Human_RBP_ID_1520335,Human_RBP_ID_1844518,Human_RBP_ID_6525343,Human_RBP_ID_8809006,Human_RBP_ID_12770933,Human_RBP_ID_17254907,Human_RBP_ID_18681687,Human_RBP_ID_26946872 RMVar_hsa_circ_95754,RMVar_hsa_circ_117018,RMVar_hsa_circ_124215,RMVar_hsa_circ_108594,RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_86225,RMVar_hsa_circ_93341,RMVar_hsa_circ_178959,RMVar_hsa_circ_178961,RMVar_hsa_circ_178962,RMVar_hsa_circ_178960,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956 92840 RMVar_ID_92840 Human_SNP_ID_606489813 m1A Human chr16 + 66723196 66723196 66723196 AACAATGATTCTTCAACTTCTACTGAATGCACAGTATTTACTGACACTGCTCATCTCCTCCTTCC AACAATGATTCTTCAACTTCTACTGAATGCACTGTATTTACTGACACTGCTCATCTCCTCCTTCC A T AC018557.1 Ensembl:ENSG00000260465 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66723145..66723300 26863196 MeRIP-seq:(Medium) rs777182006 Functional Loss SNV dbSNP153 33..33 33 - - - 92841 RMVar_ID_92841 Human_SNP_ID_606489881 m1A Human chr16 - 66723451 66723451 66723451 GTGGGAGGCAAGCACATCTGGGCTTCTTGTGGAGGGGAAGGTAGAGTGAAAGAAAGAGGGCCCAC GTGGGAGGCAAGCACATCTGGGCTTCTTGTGGTGGGGAAGGTAGAGTGAAAGAAAGAGGGCCCAC T A DYNC1LI2 Ensembl:ENSG00000135720 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66723401..66723500 26863196 MeRIP-seq:(Medium) rs556134457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233671,Human_RBP_ID_761334,Human_RBP_ID_818134,Human_RBP_ID_1178631,Human_RBP_ID_4376674,Human_RBP_ID_5524503,Human_RBP_ID_6525385,Human_RBP_ID_8809015,Human_RBP_ID_17879107,Human_RBP_ID_18163005,Human_RBP_ID_23695243 RMVar_hsa_circ_95754,RMVar_hsa_circ_117018,RMVar_hsa_circ_124215,RMVar_hsa_circ_108594,RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_86225,RMVar_hsa_circ_93341,RMVar_hsa_circ_178959,RMVar_hsa_circ_178961,RMVar_hsa_circ_178962,RMVar_hsa_circ_178960,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956 92842 RMVar_ID_92842 Human_SNP_ID_606489882 m1A Human chr16 - 66723451 66723451 66723451 GTGGGAGGCAAGCACATCTGGGCTTCTTGTGGAGGGGAAGGTAGAGTGAAAGAAAGAGGGCCCAC GTGGGAGGCAAGCACATCTGGGCTTCTTGTGGGGGGGAAGGTAGAGTGAAAGAAAGAGGGCCCAC T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66723401..66723500 26863196 MeRIP-seq:(Medium) rs556134457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233671,Human_RBP_ID_761334,Human_RBP_ID_818134,Human_RBP_ID_1178631,Human_RBP_ID_4376674,Human_RBP_ID_5524503,Human_RBP_ID_6525385,Human_RBP_ID_8809015,Human_RBP_ID_17879107,Human_RBP_ID_18163005,Human_RBP_ID_23695243 RMVar_hsa_circ_95754,RMVar_hsa_circ_117018,RMVar_hsa_circ_124215,RMVar_hsa_circ_108594,RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_86225,RMVar_hsa_circ_93341,RMVar_hsa_circ_178959,RMVar_hsa_circ_178961,RMVar_hsa_circ_178962,RMVar_hsa_circ_178960,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956 92843 RMVar_ID_92843 Human_SNP_ID_606491645 m1A Human chr16 - 66730146 66730146 66730146 AAATTTTACAACCGTGAAGCCGGAAGATGCATATGAAGACTTTATTGTGAAACCTCCCGTGAGAA AAATTTTACAACCGTGAAGCCGGAAGATGCATGTGAAGACTTTATTGTGAAACCTCCCGTGAGAA T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:66730143..66730244 32194978 MeRIP-seq:(Medium) rs750133866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233674,Human_RBP_ID_477078,Human_RBP_ID_895443,Human_RBP_ID_6525443,Human_RBP_ID_9372919,Human_RBP_ID_12771252,Human_RBP_ID_18983882,Human_RBP_ID_24544414,Human_RBP_ID_27811145 Human_Splice_Rec_1723770,Human_Splice_Rec_1723771,Human_Splice_Rec_1723792,Human_Splice_Rec_1723793,Human_Splice_Rec_1723807,Human_Splice_Rec_1723823,Human_Splice_Rec_1723833,Human_Splice_Rec_1723838,Human_Splice_Rec_1723839,Human_Splice_Rec_1723852,Human_Splice_Rec_1723853,Human_Splice_Rec_1723858,Human_Splice_Rec_1723859 Human_miRNA_ID_1523114,Human_miRNA_ID_1751835,Human_miRNA_ID_2063730,Human_miRNA_ID_2063731,Human_miRNA_ID_2901391,Human_miRNA_ID_2901392 RMVar_hsa_circ_124215,RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_2282,RMVar_hsa_circ_49120,RMVar_hsa_circ_178957,RMVar_hsa_circ_93341,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_49799,RMVar_hsa_circ_30777,RMVar_hsa_circ_109490,RMVar_hsa_circ_178965,RMVar_hsa_circ_178967,RMVar_hsa_circ_25272,RMVar_hsa_circ_178966,RMVar_hsa_circ_178969,RMVar_hsa_circ_313510,RMVar_hsa_circ_67167,RMVar_hsa_circ_319145,RMVar_hsa_circ_316889,RMVar_hsa_circ_345952,RMVar_hsa_circ_23453,RMVar_hsa_circ_127934,RMVar_hsa_circ_178971,RMVar_hsa_circ_178972,RMVar_hsa_circ_178970,RMVar_hsa_circ_178968 92844 RMVar_ID_92844 Human_SNP_ID_606491914 m1A Human chr16 + 66731436 66731436 66731436 AATCCCTGAGAGCTCCTGGCTTTCACATTTCCAGCCTCTCACAGACTGCACTCCCCGGCTCCCCC AATCCCTGAGAGCTCCTGGCTTTCACATTTCCGGCCTCTCACAGACTGCACTCCCCGGCTCCCCC A G AC018557.1,AC018557.3 Ensembl:ENSG00000260465,Ensembl:ENSG00000287965 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:66731388..66731573 26863196 MeRIP-seq:(Medium) rs976545218 Functional Loss SNV dbSNP153 33..33 33 - - - 92845 RMVar_ID_92845 Human_SNP_ID_606491935 m1A Human chr16 - 66731505 66731505 66731505 AGGGAAAGCAGGAGGGTGATGCTGGAAGACAAATGGTAGATCCCAGGCGGACTGGAAAGAATTGC AGGGAAAGCAGGAGGGTGATGCTGGAAGACAAGTGGTAGATCCCAGGCGGACTGGAAAGAATTGC T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:66731383..66731601;chr16:66731363..66731597;chr16:66731372..66731603 26863196 MeRIP-seq:(Medium) rs1401459537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760246,Human_RBP_ID_1066334,Human_RBP_ID_5087950,Human_RBP_ID_9843175,Human_RBP_ID_12771320,Human_RBP_ID_22946173,Human_RBP_ID_25245514,Human_RBP_ID_26330140 RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_93341,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_49799,RMVar_hsa_circ_30777,RMVar_hsa_circ_109490,RMVar_hsa_circ_178967,RMVar_hsa_circ_25272,RMVar_hsa_circ_178966,RMVar_hsa_circ_178969,RMVar_hsa_circ_313510,RMVar_hsa_circ_319145,RMVar_hsa_circ_316889,RMVar_hsa_circ_345952,RMVar_hsa_circ_23453,RMVar_hsa_circ_127934,RMVar_hsa_circ_178971,RMVar_hsa_circ_178972,RMVar_hsa_circ_178970,RMVar_hsa_circ_178968 92846 RMVar_ID_92846 Human_SNP_ID_606496702 m1A Human chr16 - 66749243 66749243 66749243 CTACAAGGAGCTGAGCATGGCAAAAAAGGAAGAGGCCTAGAATATCTCTACCTCAGTGTCCATGA CTACAAGGAGCTGAGCATGGCAAAAAAGGAAGGGGCCTAGAATATCTCTACCTCAGTGTCCATGA T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:66742664..66749292 32194978 MeRIP-seq:(Medium) rs1313817622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1844580,Human_RBP_ID_3947728,Human_RBP_ID_5571883,Human_RBP_ID_8231644,Human_RBP_ID_9372929,Human_RBP_ID_17879121,Human_RBP_ID_18983889,Human_RBP_ID_22801891,Human_RBP_ID_22940777,Human_RBP_ID_26330143,Human_RBP_ID_27811153 Human_Splice_Rec_1723760,Human_Splice_Rec_1723761,Human_Splice_Rec_1723784,Human_Splice_Rec_1723785,Human_Splice_Rec_1723876,Human_Splice_Rec_1723877,Human_Splice_Rec_1723884,Human_Splice_Rec_1723885,Human_Splice_Rec_1723892,Human_Splice_Rec_1723893 Human_miRNA_ID_1929613,Human_miRNA_ID_1932064 RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_93341,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_109490,RMVar_hsa_circ_178967,RMVar_hsa_circ_25272,RMVar_hsa_circ_319145,RMVar_hsa_circ_316889,RMVar_hsa_circ_78309,RMVar_hsa_circ_88939,RMVar_hsa_circ_178968,RMVar_hsa_circ_178973,RMVar_hsa_circ_178974,RMVar_hsa_circ_296572,RMVar_hsa_circ_334386,RMVar_hsa_circ_178977,RMVar_hsa_circ_370557 92847 RMVar_ID_92847 Human_SNP_ID_606496714 m1A Human chr16 - 66749290 66749290 66749290 CCTTTGTAGGTGAAGATGGTTCTGGTAAAACAACCCTCATGACTAAACTACAAGGAGCTGAGCAT CCTTTGTAGGTGAAGATGGTTCTGGTAAAACAGCCCTCATGACTAAACTACAAGGAGCTGAGCAT T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:66749165..66749342 26863196 MeRIP-seq:(Medium) rs760882886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895455,Human_RBP_ID_1520402,Human_RBP_ID_1844580,Human_RBP_ID_3947728,Human_RBP_ID_8231645,Human_RBP_ID_9063760,Human_RBP_ID_9285155,Human_RBP_ID_9372929,Human_RBP_ID_17879122,Human_RBP_ID_18681746,Human_RBP_ID_18986444,Human_RBP_ID_27811153 Human_Splice_Rec_1723760,Human_Splice_Rec_1723761,Human_Splice_Rec_1723784,Human_Splice_Rec_1723785,Human_Splice_Rec_1723876,Human_Splice_Rec_1723877,Human_Splice_Rec_1723884,Human_Splice_Rec_1723885,Human_Splice_Rec_1723892,Human_Splice_Rec_1723893 Human_miRNA_ID_2294344 RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_178957,RMVar_hsa_circ_93341,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_109490,RMVar_hsa_circ_178967,RMVar_hsa_circ_25272,RMVar_hsa_circ_319145,RMVar_hsa_circ_316889,RMVar_hsa_circ_78309,RMVar_hsa_circ_88939,RMVar_hsa_circ_178968,RMVar_hsa_circ_178973,RMVar_hsa_circ_178974,RMVar_hsa_circ_296572,RMVar_hsa_circ_334386,RMVar_hsa_circ_178977,RMVar_hsa_circ_370557 92848 RMVar_ID_92848 Human_SNP_ID_606497321 m1A Human chr16 - 66751388 66751383 66751388 CACTGAGGGGCCGACGCGAGCCGGGCCATCCCAGCCCGGCCCGGGGCTGACCACTCTTGCCATTG CACTGAGGGGCCGACGCGAGCCGGGCCATCCC_____GGCCCGGGGCTGACCACTCTTGCCATTG CGGGCT C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:66751373..66751518 26863410 MeRIP-seq:(Medium) rs1314518274 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_5355894,Human_RBP_ID_6525575,Human_RBP_ID_19071715,Human_RBP_ID_22541648,Human_RBP_ID_22652145 RMVar_hsa_circ_93341,RMVar_hsa_circ_178955 92849 RMVar_ID_92849 Human_SNP_ID_606497330 m1A Human chr16 - 66751388 66751388 66751388 CACTGAGGGGCCGACGCGAGCCGGGCCATCCCAGCCCGGCCCGGGGCTGACCACTCTTGCCATTG CACTGAGGGGCCGACGCGAGCCGGGCCATCCCGGCCCGGCCCGGGGCTGACCACTCTTGCCATTG T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:66751373..66751518 26863410 MeRIP-seq:(Medium) rs373201543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355894,Human_RBP_ID_6525575,Human_RBP_ID_19071715,Human_RBP_ID_22541648,Human_RBP_ID_22652145 RMVar_hsa_circ_93341,RMVar_hsa_circ_178955 92850 RMVar_ID_92850 Human_SNP_ID_606517030 m1A Human chr16 - 66830909 66830909 66830909 CTCCGCAGGGGCTCGGCTGTTTTCCGCGCGGCAGGCGCGGCCATGGCGCAGCTGGGAAAGCTGCT CTCCGCAGGGGCTCGGCTGTTTTCCGCGCGGCGGGCGCGGCCATGGCGCAGCTGGGAAAGCTGCT T C NAE1 Ensembl:ENSG00000159593 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66830792..66830917 26863196 MeRIP-seq:(Medium) rs886401227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477121,Human_RBP_ID_4393166,Human_RBP_ID_22054123,Human_RBP_ID_22441041 Human_Splice_Rec_1724065,Human_Splice_Rec_1724111,Human_Splice_Rec_1724155,Human_Splice_Rec_1724195,Human_Splice_Rec_1724237,Human_Splice_Rec_1724251,Human_Splice_Rec_1724263,Human_Splice_Rec_1724285,Human_Splice_Rec_1724299,Human_Splice_Rec_1724309,Human_Splice_Rec_1724323,Human_Splice_Rec_1724335,Human_Splice_Rec_1724345,Human_Splice_Rec_1724353,Human_Splice_Rec_1724359 92851 RMVar_ID_92851 Human_SNP_ID_606517031 m1A Human chr16 - 66830909 66830909 66830909 CTCCGCAGGGGCTCGGCTGTTTTCCGCGCGGCAGGCGCGGCCATGGCGCAGCTGGGAAAGCTGCT CTCCGCAGGGGCTCGGCTGTTTTCCGCGCGGCCGGCGCGGCCATGGCGCAGCTGGGAAAGCTGCT T G NAE1 Ensembl:ENSG00000159593 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66830792..66830917 26863196 MeRIP-seq:(Medium) rs886401227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477121,Human_RBP_ID_4393166,Human_RBP_ID_22054123,Human_RBP_ID_22441041 Human_Splice_Rec_1724065,Human_Splice_Rec_1724111,Human_Splice_Rec_1724155,Human_Splice_Rec_1724195,Human_Splice_Rec_1724237,Human_Splice_Rec_1724251,Human_Splice_Rec_1724263,Human_Splice_Rec_1724285,Human_Splice_Rec_1724299,Human_Splice_Rec_1724309,Human_Splice_Rec_1724323,Human_Splice_Rec_1724335,Human_Splice_Rec_1724345,Human_Splice_Rec_1724353,Human_Splice_Rec_1724359 92852 RMVar_ID_92852 Human_SNP_ID_606541337 m1A Human chr16 - 66924869 66924869 66924869 GGTGCTGCTGCTGGGGGCGCCCGGCGTGGGCAAGAGCGCCCTGGCGCGCATCTTCGGCGGTGTGG GGTGCTGCTGCTGGGGGCGCCCGGCGTGGGCATGAGCGCCCTGGCGCGCATCTTCGGCGGTGTGG T A RRAD Ensembl:ENSG00000166592 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66924818..66924992 26863196 MeRIP-seq:(Medium) rs754757202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1724663,Human_Splice_Rec_1724671,Human_Splice_Rec_1724679,Human_Splice_Rec_1724683 92853 RMVar_ID_92853 Human_SNP_ID_606543391 m1A Human chr16 - 66932849 66932849 66932849 AGGGAAAAGTGTGGGTCGGTGGGTGGGTGTTCAGGCCCTGGTTATCTCCCTCCCAGATGGACGTG AGGGAAAAGTGTGGGTCGGTGGGTGGGTGTTCGGGCCCTGGTTATCTCCCTCCCAGATGGACGTG T C CIAO2B Ensembl:ENSG00000166595 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66932844..66932971 26863196 MeRIP-seq:(Medium) rs1016248146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780489 Human_Splice_Rec_1724693,Human_Splice_Rec_1724701,Human_Splice_Rec_1724709,Human_Splice_Rec_1724715,Human_Splice_Rec_1724723 RMVar_hsa_circ_103379,RMVar_hsa_circ_107703,RMVar_hsa_circ_94109,RMVar_hsa_circ_179001,RMVar_hsa_circ_179003,RMVar_hsa_circ_179002 92854 RMVar_ID_92854 Human_SNP_ID_606543656 m1A Human chr16 + 66933711 66933711 66933711 TGCTGCAGTGCGGAATGGTTGGTGTGAAAGCCACAGCCACTGTACTCTCGGGGTCGCTAACCTGG TGCTGCAGTGCGGAATGGTTGGTGTGAAAGCCCCAGCCACTGTACTCTCGGGGTCGCTAACCTGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:66933661..66933780 26863196 MeRIP-seq:(Medium) rs779007005 Functional Loss SNV dbSNP153 33..33 33 - - - 92855 RMVar_ID_92855 Human_SNP_ID_606543884 m1A Human chr16 - 66934267 66934267 66934267 CTCTGGGGAGCGGCCTGTGACGGCAGGCGAGGAGGACGAGCAGGTTCCCGACAGCATCGACGCAC CTCTGGGGAGCGGCCTGTGACGGCAGGCGAGGGGGACGAGCAGGTTCCCGACAGCATCGACGCAC T C CIAO2B Ensembl:ENSG00000166595 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:66933976..66934379 26863196 MeRIP-seq:(Medium) rs770135318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477163,Human_RBP_ID_1520434,Human_RBP_ID_4376903,Human_RBP_ID_17883528 Human_Splice_Rec_1724703 RMVar_hsa_circ_103379,RMVar_hsa_circ_179001 92856 RMVar_ID_92856 Human_SNP_ID_606543909 m1A Human chr16 - 66934325 66934325 66934325 GCGGCGGCGGGGTCGGCGGCGGCCTCCTGGAGAATGCCAACCCCCTCATCTACCAGCGCTCTGGG GCGGCGGCGGGGTCGGCGGCGGCCTCCTGGAGGATGCCAACCCCCTCATCTACCAGCGCTCTGGG T C CIAO2B Ensembl:ENSG00000166595 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:66934201..66934375 26863196 MeRIP-seq:(Medium) rs1312432426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477165,Human_RBP_ID_4376904,Human_RBP_ID_5317580,Human_RBP_ID_5495918,Human_RBP_ID_17883528,Human_RBP_ID_22441556,Human_RBP_ID_26946967 Human_Splice_Rec_1724703 RMVar_hsa_circ_103379,RMVar_hsa_circ_179001 92857 RMVar_ID_92857 Human_SNP_ID_606543910 m1A Human chr16 - 66934325 66934325 66934325 GCGGCGGCGGGGTCGGCGGCGGCCTCCTGGAGAATGCCAACCCCCTCATCTACCAGCGCTCTGGG GCGGCGGCGGGGTCGGCGGCGGCCTCCTGGAGCATGCCAACCCCCTCATCTACCAGCGCTCTGGG T G CIAO2B Ensembl:ENSG00000166595 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:66934201..66934375 26863196 MeRIP-seq:(Medium) rs1312432426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477165,Human_RBP_ID_4376904,Human_RBP_ID_5317580,Human_RBP_ID_5495918,Human_RBP_ID_17883528,Human_RBP_ID_22441556,Human_RBP_ID_26946967 Human_Splice_Rec_1724703 RMVar_hsa_circ_103379,RMVar_hsa_circ_179001 92858 RMVar_ID_92858 Human_SNP_ID_606543917 m1A Human chr16 + 66934333 66934333 66934333 GCTGGTAGATGAGGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGACCCCGCCGCCGCCTACCATC GCTGGTAGATGAGGGGGTTGGCATTCTCCAGGCGGCCGCCGCCGACCCCGCCGCCGCCTACCATC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:66934053..66934400 26863196 MeRIP-seq:(Medium) rs1366839114 Functional Loss SNV dbSNP153 33..33 33 - - - 92859 RMVar_ID_92859 Human_SNP_ID_606543933 m1A Human chr16 + 66934345 66934345 66934345 GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGACCCCGCCGCCGCCTACCATCGCGGAACCACCA GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGCCCCCGCCGCCGCCTACCATCGCGGAACCACCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:66934139..66934375 26863196 MeRIP-seq:(Medium) rs1427505058 Functional Loss SNV dbSNP153 33..33 33 - - - 92860 RMVar_ID_92860 Human_SNP_ID_606543934 m1A Human chr16 + 66934345 66934345 66934345 GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGACCCCGCCGCCGCCTACCATCGCGGAACCACCA GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGTCCCCGCCGCCGCCTACCATCGCGGAACCACCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:66934139..66934375 26863196 MeRIP-seq:(Medium) rs1427505058 Functional Loss SNV dbSNP153 33..33 33 - - - 92861 RMVar_ID_92861 Human_SNP_ID_606544054 m1A Human chr16 + 66934550 66934550 66934550 GACCGCGGCCCTGGCTGCTCGGACCCGGGAACATGATGGTCGCTGGAGCAGAAGGCGCTGAGAAG GACCGCGGCCCTGGCTGCTCGGACCCGGGAACGTGATGGTCGCTGGAGCAGAAGGCGCTGAGAAG A G CES2 Ensembl:ENSG00000172831 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:66934501..66934670 26863196 MeRIP-seq:(Medium) rs1427862254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393897,Human_RBP_ID_5524505 RMVar_hsa_circ_127527,RMVar_hsa_circ_179006 92862 RMVar_ID_92862 Human_SNP_ID_606544292 m1A Human chr16 + 66935473 66935473 66935473 CCTATGACTGCTCAGTCCCGCTCTCCTACCACACCCACCTTTCCCGGCCCAAGCCAGCGCACCCC CCTATGACTGCTCAGTCCCGCTCTCCTACCACCCCCACCTTTCCCGGCCCAAGCCAGCGCACCCC A C CES2 Ensembl:ENSG00000172831 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:66935424..66935516 26863196 MeRIP-seq:(Medium) rs767099099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4376955,Human_RBP_ID_5142889,Human_RBP_ID_5495920,Human_RBP_ID_27443979 RMVar_hsa_circ_127527,RMVar_hsa_circ_179006 92863 RMVar_ID_92863 Human_SNP_ID_606546986 m1A Human chr16 + 66944602 66944602 66944602 AACCCCATCTCTATGAAAAATACAAAAATCAGACGGGCACAGTGGTGGTGCCCACCTGTGATCCC AACCCCATCTCTATGAAAAATACAAAAATCAGCCGGGCACAGTGGTGGTGCCCACCTGTGATCCC A C AC009084.1,CES2 Ensembl:ENSG00000265408,Ensembl:ENSG00000172831 lincRNA,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:66944556..66944630 26863196 MeRIP-seq:(Medium) rs900913356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477193,Human_RBP_ID_760100,Human_RBP_ID_8188372,Human_RBP_ID_17690624,Human_RBP_ID_17879179 RMVar_hsa_circ_112490,RMVar_hsa_circ_179010 92864 RMVar_ID_92864 Human_SNP_ID_606547055 m1A Human chr16 + 66944894 66944894 66944894 TGGGCAAACCCCGGTGGAATCCCACCCTCCCCAACACCCCACTGAGCCCTGGGCCCCCTCCTCCC TGGGCAAACCCCGGTGGAATCCCACCCTCCCCCACACCCCACTGAGCCCTGGGCCCCCTCCTCCC A C AC009084.1,CES2 Ensembl:ENSG00000265408,Ensembl:ENSG00000172831 lincRNA,Protein coding intron,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:66944844..66944980 26863196 MeRIP-seq:(Medium) rs1478425455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477196,Human_RBP_ID_4377061,Human_RBP_ID_5465319,Human_RBP_ID_8188373,Human_RBP_ID_18939236,Human_RBP_ID_27443990 RMVar_hsa_circ_112490,RMVar_hsa_circ_179010 92865 RMVar_ID_92865 Human_SNP_ID_606547086 m1A Human chr16 - 66944994 66944994 66944994 GTGTGGGCAACATTCTTCGAAGCACCTCCCTCAAAGTGGAAAAGGCCTGGGGGCTCAGACGAGAG GTGTGGGCAACATTCTTCGAAGCACCTCCCTCTAAGTGGAAAAGGCCTGGGGGCTCAGACGAGAG T A AC009084.3 Ensembl:ENSG00000280416 Other exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66944944..66945037 26863196 MeRIP-seq:(Medium) rs1359113390 Functional Loss SNV dbSNP153 33..33 33 - - - 92866 RMVar_ID_92866 Human_SNP_ID_606568795 m1A Human chr16 - 67029698 67029698 67029698 TAATCTGCAAGGCAAGACGGCCCGAAATCAGGAGCCAAATCCGCGGCGCCGCCCGCGCGCCCGCC TAATCTGCAAGGCAAGACGGCCCGAAATCAGGGGCCAAATCCGCGGCGCCGCCCGCGCGCCCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67029695..67029849 26863196 MeRIP-seq:(Medium) rs756781303 Functional Loss SNV dbSNP153 33..33 33 - - - 92867 RMVar_ID_92867 Human_SNP_ID_606578878 m1A Human chr16 + 67066785 67066785 67066785 ACTGGATGGTATGGGCTGTCTGGAGTTTGATGAGGAGCGAGCCCAGGTAGGGTAACATCAGGCTT ACTGGATGGTATGGGCTGTCTGGAGTTTGATGGGGAGCGAGCCCAGGTAGGGTAACATCAGGCTT A G CBFB Ensembl:ENSG00000067955 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67066637..67066843 26863196 MeRIP-seq:(Medium) rs113484034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43696,Human_RBP_ID_894833,Human_RBP_ID_23118478,Human_RBP_ID_26329067,Human_RBP_ID_26810452 Human_Splice_Rec_1725119,Human_Splice_Rec_1725131,Human_Splice_Rec_1725141,Human_Splice_Rec_1725151,Human_Splice_Rec_1725161,Human_Splice_Rec_1725169,Human_Splice_Rec_1725177,Human_Splice_Rec_1725189 Human_miRNA_ID_2554717,Human_miRNA_ID_2554718,Human_miRNA_ID_2554719 RMVar_hsa_circ_99066,RMVar_hsa_circ_179019,RMVar_hsa_circ_80501,RMVar_hsa_circ_179021,RMVar_hsa_circ_281379,RMVar_hsa_circ_289906,RMVar_hsa_circ_291214,RMVar_hsa_circ_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_179020,RMVar_hsa_circ_349193,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023,RMVar_hsa_circ_179024 92868 RMVar_ID_92868 Human_SNP_ID_606584191 m1A Human chr16 + 67086990 67086990 67086990 TTTGAAGGAAGAGTGTGTTTTGCCAGCTGTTCAAGTTGGAGAAAGCATTCTGGGCAGGACAAACA TTTGAAGGAAGAGTGTGTTTTGCCAGCTGTTCGAGTTGGAGAAAGCATTCTGGGCAGGACAAACA A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67086985..67087077 26863196 MeRIP-seq:(Medium) rs937550811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80501,RMVar_hsa_circ_179023 92869 RMVar_ID_92869 Human_SNP_ID_606587227 m1A Human chr16 - 67099188 67099187 67099188 GCTCATCTAAAATGAAGCTGTATAACCAAAACATCTAGAAGTACAAAAAAAAAAATAGAAAAAAT GCTCATCTAAAATGAAGCTGTATAACCAAAAC_TCTAGAAGTACAAAAAAAAAAATAGAAAAAAT AT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:67099096..67099188 32194978 MeRIP-seq:(Medium) rs1567628537 Functional Loss DEL dbSNP153 33..33 33 - - - 92870 RMVar_ID_92870 Human_SNP_ID_606591416 m1A Human chr16 + 67115033 67115033 67115033 GGTTAGTTGAACCAGGGATGAGCAGAAGAAACATAGCCTATTGGAGAGACTTGGAAAAGTTAGAG GGTTAGTTGAACCAGGGATGAGCAGAAGAAACGTAGCCTATTGGAGAGACTTGGAAAAGTTAGAG A G C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67115021..67115104 26863196 MeRIP-seq:(Medium) rs148823364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179025,RMVar_hsa_circ_90176 92871 RMVar_ID_92871 Human_SNP_ID_606598108 m1A Human chr16 - 67142978 67142978 67142978 AACCTCTGACTCTACCCCTGTACCCACAGCCAACTAAGTCCTACTGAGGCCAGTCCATTCTCTCC AACCTCTGACTCTACCCCTGTACCCACAGCCATCTAAGTCCTACTGAGGCCAGTCCATTCTCTCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67142954..67143075 26863196 MeRIP-seq:(Medium) rs956130568 Functional Loss SNV dbSNP153 33..33 33 - - - 92872 RMVar_ID_92872 Human_SNP_ID_606598109 m1A Human chr16 - 67142978 67142978 67142978 AACCTCTGACTCTACCCCTGTACCCACAGCCAACTAAGTCCTACTGAGGCCAGTCCATTCTCTCC AACCTCTGACTCTACCCCTGTACCCACAGCCAGCTAAGTCCTACTGAGGCCAGTCCATTCTCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67142954..67143075 26863196 MeRIP-seq:(Medium) rs956130568 Functional Loss SNV dbSNP153 33..33 33 - - - 92873 RMVar_ID_92873 Human_SNP_ID_606598125 m1A Human chr16 + 67143030 67143030 67143030 AGAGTCAGAGGTTACCCTGAGGTCACGGGCCCAAGCAGCTGGATGGATATGAAGCTGGAAAGGGT AGAGTCAGAGGTTACCCTGAGGTCACGGGCCCCAGCAGCTGGATGGATATGAAGCTGGAAAGGGT A C C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67142982..67143105 26863196 MeRIP-seq:(Medium) rs1004318499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6526409,Human_RBP_ID_12774163 RMVar_hsa_circ_179025,RMVar_hsa_circ_90176 92874 RMVar_ID_92874 Human_SNP_ID_606600436 m1A Human chr16 - 67150465 67150465 67150465 GGCCGCGCGGAGATGAGGAGGAGGCTGCGCCTACGCAGGGACGCATTGCTCACGCTGCTCCTTGG GGCCGCGCGGAGATGAGGAGGAGGCTGCGCCTCCGCAGGGACGCATTGCTCACGCTGCTCCTTGG T G B3GNT9 Ensembl:ENSG00000237172 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67150427..67150576 26863196 MeRIP-seq:(Medium) rs1414695989 Functional Loss SNV dbSNP153 33..33 33 - - - 92875 RMVar_ID_92875 Human_SNP_ID_606600618 m1A Human chr16 - 67150940 67150940 67150940 TGCCAACGCTGCATTTGGCTCGGGCCCGGTCCATGGCGGCCCCTCGGACCCTGCGCTGAGCCCCG TGCCAACGCTGCATTTGGCTCGGGCCCGGTCCTTGGCGGCCCCTCGGACCCTGCGCTGAGCCCCG T A B3GNT9 Ensembl:ENSG00000237172 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67150699..67150955 26863196 MeRIP-seq:(Medium) rs1001729621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1725353 92876 RMVar_ID_92876 Human_SNP_ID_606600619 m1A Human chr16 - 67150940 67150940 67150940 TGCCAACGCTGCATTTGGCTCGGGCCCGGTCCATGGCGGCCCCTCGGACCCTGCGCTGAGCCCCG TGCCAACGCTGCATTTGGCTCGGGCCCGGTCCCTGGCGGCCCCTCGGACCCTGCGCTGAGCCCCG T G B3GNT9 Ensembl:ENSG00000237172 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67150699..67150955 26863196 MeRIP-seq:(Medium) rs1001729621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1725353 92877 RMVar_ID_92877 Human_SNP_ID_606602154 m1A Human chr16 - 67155652 67155652 67155652 CGCCCGGCGCCTGACCGCCCGCCTCCGCAGAGAGCGGCGGGAGCCCGGACGTGCTGCAGATGCTG CGCCCGGCGCCTGACCGCCCGCCTCCGCAGAGGGCGGCGGGAGCCCGGACGTGCTGCAGATGCTG T C TRADD Ensembl:ENSG00000102871 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67155498..67155667 26863196 MeRIP-seq:(Medium) rs754990814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477361,Human_RBP_ID_22653152 Human_Splice_Rec_1725358 RMVar_hsa_circ_78411,RMVar_hsa_circ_179033 92878 RMVar_ID_92878 Human_SNP_ID_606604369 m1A Human chr16 + 67163562 67163562 67163562 GCGCTGCGCCTCAACCTCTCAGGCGACACCGTAGGCCCAGTGCGCTTCGCAGCACACCACTACGC GCGCTGCGCCTCAACCTCTCAGGCGACACCGTCGGCCCAGTGCGCTTCGCAGCACACCACTACGC A C AC074143.1,FBXL8 Ensembl:ENSG00000265690,Ensembl:ENSG00000135722 Protein coding,Protein coding CDS,stop codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:67163425..67163692 26863196 MeRIP-seq:(Medium) rs1267738109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1725380 92879 RMVar_ID_92879 Human_SNP_ID_606604400 m1A Human chr16 + 67163615 67163603 67163616 ACACCACTACGCCGCAACCCTGTGCGCGCTCGAGGTGCGCGCAGCCGCTTCGGCCGAGCTGAACG ACACCACTACGCCGCAACCCT_____________GTGCGCGCAGCCGCTTCGGCCGAGCTGAACG TGTGCGCGCTCGAG T AC074143.1,FBXL8 Ensembl:ENSG00000265690,Ensembl:ENSG00000135722 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:67163532..67163666 26863196 MeRIP-seq:(Medium) rs752265284 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_477364 92880 RMVar_ID_92880 Human_SNP_ID_606604476 m1A Human chr16 - 67163726 67163726 67163726 GCAGGCGCGGGCAGTGCGCGCGGAAGGCGTCCAGCACCGAGTGGCTCACCACGCAGAAACAATGC GCAGGCGCGGGCAGTGCGCGCGGAAGGCGTCCGGCACCGAGTGGCTCACCACGCAGAAACAATGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67163675..67163825 32194978 MeRIP-seq:(Medium) rs762161864 Functional Loss SNV dbSNP153 33..33 33 - - - 92881 RMVar_ID_92881 Human_SNP_ID_606604668 m1A Human chr16 - 67164139 67164139 67164139 TGCAGGATTTGTTTATTTCACACTCACCCTTGAGGCCCGGCCCGCGCCCGTGCCCTCCCTCTCCC TGCAGGATTTGTTTATTTCACACTCACCCTTGGGGCCCGGCCCGCGCCCGTGCCCTCCCTCTCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67164122..67164272 32194978 MeRIP-seq:(Medium) rs1470372882 Functional Loss SNV dbSNP153 33..33 33 - - - 92882 RMVar_ID_92882 Human_SNP_ID_606607178 m1A Human chr16 + 67171455 67171455 67171455 AGCATCAGCAAAGGCTCCGAGGTGCCAGAGGCATAGTGAGTTCTCCGATCCCTGGCTGGTGGAGG AGCATCAGCAAAGGCTCCGAGGTGCCAGAGGCTTAGTGAGTTCTCCGATCCCTGGCTGGTGGAGG A T NOL3 Ensembl:ENSG00000140939 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67171424..67171549 26863196 MeRIP-seq:(Medium) rs1264408064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1725775,Human_Splice_Rec_1725785 92883 RMVar_ID_92883 Human_SNP_ID_606607193 m1A Human chr16 + 67171497 67171496 67171497 CTCCGATCCCTGGCTGGTGGAGGGAAGCTGGGAAGGGCCTGGCTGTCCAGGGTGGTGGGAGGAGG CTCCGATCCCTGGCTGGTGGAGGGAAGCTGGG_AGGGCCTGGCTGTCCAGGGTGGTGGGAGGAGG GA G NOL3 Ensembl:ENSG00000140939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67171272..67171563 26863196 MeRIP-seq:(Medium) rs1377838353 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_234900,Human_RBP_ID_762612,Human_RBP_ID_18939237 92884 RMVar_ID_92884 Human_SNP_ID_606607311 m1A Human chr16 + 67172007 67172007 67172007 GAAGCCAGGGTGTGAAGTGACGGGGGAGGTATAGTGTGACACCAGAGGGTACTGAGAAAGACCTG GAAGCCAGGGTGTGAAGTGACGGGGGAGGTATGGTGTGACACCAGAGGGTACTGAGAAAGACCTG A G NOL3 Ensembl:ENSG00000140939 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:67171707..67172780;chr16:67171747..67172780 26863196 MeRIP-seq:(Medium) rs1192279916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947752,Human_RBP_ID_9419291,Human_RBP_ID_23274552,Human_RBP_ID_23695712,Human_RBP_ID_24551947 92885 RMVar_ID_92885 Human_SNP_ID_606607719 m1A Human chr16 + 67173480 67173480 67173480 GTGGGAGGGTGTAGAGGCGGGGCTTGTCCTGGAAAGTTGGATATCAGGGTCAAGGTAAGGGGAGA GTGGGAGGGTGTAGAGGCGGGGCTTGTCCTGGCAAGTTGGATATCAGGGTCAAGGTAAGGGGAGA A C NOL3 Ensembl:ENSG00000140939 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67173464..67173647 26863196 MeRIP-seq:(Medium) rs563235961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509087,Human_RBP_ID_23274554,Human_RBP_ID_26445229 92886 RMVar_ID_92886 Human_SNP_ID_606607720 m1A Human chr16 + 67173480 67173480 67173480 GTGGGAGGGTGTAGAGGCGGGGCTTGTCCTGGAAAGTTGGATATCAGGGTCAAGGTAAGGGGAGA GTGGGAGGGTGTAGAGGCGGGGCTTGTCCTGGGAAGTTGGATATCAGGGTCAAGGTAAGGGGAGA A G NOL3 Ensembl:ENSG00000140939 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67173464..67173647 26863196 MeRIP-seq:(Medium) rs563235961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509087,Human_RBP_ID_23274554,Human_RBP_ID_26445229 92887 RMVar_ID_92887 Human_SNP_ID_606607998 m1A Human chr16 - 67174321 67174321 67174321 GTAGGCGGCGCACCCTGCGCTCGGCATCAGGCAGTGCATCCAATGCCTCGTACTCTGGCCCGGTG GTAGGCGGCGCACCCTGCGCTCGGCATCAGGCGGTGCATCCAATGCCTCGTACTCTGGCCCGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67174158..67174320 26863196 MeRIP-seq:(Medium) rs1479752275 Functional Loss SNV dbSNP153 33..33 33 - - - 92888 RMVar_ID_92888 Human_SNP_ID_606608285 m1A Human chr16 - 67174862 67174860 67174862 TCTGGCTCCAGTTCCGGCTCTGGTTCTGCTTCAGCCTCGGGTTCCAGCTCTGGCTCTGGCTCCGG TCTGGCTCCAGTTCCGGCTCTGGTTCTGCTTC__CCTCGGGTTCCAGCTCTGGCTCTGGCTCCGG GCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67174811..67174882 26863196 MeRIP-seq:(Medium) rs1193628741 Functional Loss DEL dbSNP153 33..34 33 - - - 92889 RMVar_ID_92889 Human_SNP_ID_606610074 m1A Human chr16 - 67180615 67180615 67180615 TTGGAGTGACCCGGCTGGATGTGACCCCCAGGACAGAATGGTGCTGGACTCAGGGGCTCAGGCGT TTGGAGTGACCCGGCTGGATGTGACCCCCAGGGCAGAATGGTGCTGGACTCAGGGGCTCAGGCGT T C KIAA0895L Ensembl:ENSG00000196123 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67180565..67180688 26863196 MeRIP-seq:(Medium) rs770258958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892284,Human_RBP_ID_3947757,Human_RBP_ID_9372942,Human_RBP_ID_18681919 Human_Splice_Rec_1725812,Human_Splice_Rec_1725840,Human_Splice_Rec_1725854 RMVar_hsa_circ_179036 92890 RMVar_ID_92890 Human_SNP_ID_606610655 m1A Human chr16 - 67183416 67183416 67183416 TCTGAGTAAAGAAGTCGCCGAAGCAGTGGGACACTAGACGCGGGGAAGGCTTCCTGGAGGAAGTG TCTGAGTAAAGAAGTCGCCGAAGCAGTGGGACCCTAGACGCGGGGAAGGCTTCCTGGAGGAAGTG T G KIAA0895L Ensembl:ENSG00000196123 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67183366..67183510 26863196 MeRIP-seq:(Medium) rs1238266754 Functional Loss SNV dbSNP153 33..33 33 - - - 92891 RMVar_ID_92891 Human_SNP_ID_606613606 m1A Human chr16 + 67192228 67192228 67192228 GCCTGGCTGAGGGGAGGCGGCGGGCGGGCGCGATGGCGGAGGCCGGGCCACAGGCGCCGCCGCCC GCCTGGCTGAGGGGAGGCGGCGGGCGGGCGCGGTGGCGGAGGCCGGGCCACAGGCGCCGCCGCCC A G E2F4 Ensembl:ENSG00000205250 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:67192176..67192325;chr16:67192176..67192350 26863196 MeRIP-seq:(Medium) rs1211826296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235236,Human_RBP_ID_763792,Human_RBP_ID_4393176,Human_RBP_ID_9325160 92892 RMVar_ID_92892 Human_SNP_ID_606614492 m1A Human chr16 + 67194822 67194822 67194822 TGTGCCTGTGCCACCACCTGAAGATTTGCTCCAGAGCCCATCTGCTGTTTCTACACCTCCACCTC TGTGCCTGTGCCACCACCTGAAGATTTGCTCCGGAGCCCATCTGCTGTTTCTACACCTCCACCTC A G E2F4 Ensembl:ENSG00000205250 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67194772..67194865 26863196 MeRIP-seq:(Medium) rs1462325357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477404,Human_RBP_ID_1520501,Human_RBP_ID_8436533,Human_RBP_ID_22053269,Human_RBP_ID_26442529 Human_miRNA_ID_2793446,Human_miRNA_ID_3069762 RMVar_hsa_circ_64904,RMVar_hsa_circ_376029,RMVar_hsa_circ_330244,RMVar_hsa_circ_82573,RMVar_hsa_circ_179038,RMVar_hsa_circ_179039,RMVar_hsa_circ_179040 92893 RMVar_ID_92893 Human_SNP_ID_606621315 m1A Human chr16 - 67216054 67216050 67216054 AAGAAGTCTTCTGGAAGCAAAAGAGCAGGAGAAGGAGGAAGGTTCAGATGGGCCCTGCCTGGAGG AAGAAGTCTTCTGGAAGCAAAAGAGCAGGAGA____GGAAGGTTCAGATGGGCCCTGCCTGGAGG CTCCT C LRRC29 Ensembl:ENSG00000125122 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67215997..67216434 26863196 MeRIP-seq:(Medium) rs991653115 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_121517,RMVar_hsa_circ_179042 92894 RMVar_ID_92894 Human_SNP_ID_606621316 m1A Human chr16 - 67216054 67216052 67216055 AAGAAGTCTTCTGGAAGCAAAAGAGCAGGAGAAGGAGGAAGGTTCAGATGGGCCCTGCCTGGAGG AAGAAGTCTTCTGGAAGCAAAAGAGCAGGAG___GAGGAAGGTTCAGATGGGCCCTGCCTGGAGG CCTT C LRRC29 Ensembl:ENSG00000125122 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67215997..67216434 26863196 MeRIP-seq:(Medium) rs1252520024 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_121517,RMVar_hsa_circ_179042 92895 RMVar_ID_92895 Human_SNP_ID_606621328 m1A Human chr16 - 67216117 67216115 67216118 TGGAAAGGCATAAACATCAGGGTTCTCAGAGGAGAAGGTGCAGCAGGAGAAGGAGGCCAGGAGAA TGGAAAGGCATAAACATCAGGGTTCTCAGAG___AAGGTGCAGCAGGAGAAGGAGGCCAGGAGAA TCTC T LRRC29 Ensembl:ENSG00000125122 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67216086..67216370 26863196 MeRIP-seq:(Medium) rs1302113179 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_121517,RMVar_hsa_circ_179042 92896 RMVar_ID_92896 Human_SNP_ID_606627241 m1A Human chr16 + 67236646 67236646 67236646 AAAAGGTTCACTGAAGCTTGGAGACCGGAGGGAGGGCCCACAGGGCTGGAGGCGGGGCCTGTCAG AAAAGGTTCACTGAAGCTTGGAGACCGGAGGGCGGGCCCACAGGGCTGGAGGCGGGGCCTGTCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67236601..67236700 26863196 MeRIP-seq:(Medium) rs747988511 Functional Loss SNV dbSNP153 33..33 33 - - - 92897 RMVar_ID_92897 Human_SNP_ID_606633421 m1A Human chr16 + 67260607 67260607 67260607 AGCGGTGGGAAAGAAGAGGGGCACGTAGGCCTAGGTGATTGGCTCTGATGGTGAGAGGAGGAGGA AGCGGTGGGAAAGAAGAGGGGCACGTAGGCCTCGGTGATTGGCTCTGATGGTGAGAGGAGGAGGA A C SLC9A5 Ensembl:ENSG00000135740 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67260560..67260693 26863196 MeRIP-seq:(Medium) rs996497803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23695851 RMVar_hsa_circ_99910,RMVar_hsa_circ_115359,RMVar_hsa_circ_179065,RMVar_hsa_circ_179062,RMVar_hsa_circ_179063,RMVar_hsa_circ_371114 92898 RMVar_ID_92898 Human_SNP_ID_606633841 m1A Human chr16 + 67262755 67262754 67262756 AACACTGAGGAGTGCGCATGGGAGAAAAGGAAAGAGAGCCAAAGACAAGGAACCCTTGGAGAAGC AACACTGAGGAGTGCGCATGGGAGAAAAGGAA__AGAGCCAAAGACAAGGAACCCTTGGAGAAGC AAG A SLC9A5,AC040160.1 Ensembl:ENSG00000135740,Ensembl:ENSG00000262691 Protein coding,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67262706..67262865 26863196 MeRIP-seq:(Medium) rs1335879963 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5575412 RMVar_hsa_circ_99910,RMVar_hsa_circ_115359,RMVar_hsa_circ_179065,RMVar_hsa_circ_179062,RMVar_hsa_circ_179063,RMVar_hsa_circ_371114 92899 RMVar_ID_92899 Human_SNP_ID_606675354 m1A Human chr16 - 67432719 67432719 67432719 CCCTTGTGCCTCCTTCCCCCCTACTCTGCCTCAGCAGTCTGGCTTCTTACCTGATTCATGGCCCC CCCTTGTGCCTCCTTCCCCCCTACTCTGCCTCGGCAGTCTGGCTTCTTACCTGATTCATGGCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67432669..67432817 26863196 MeRIP-seq:(Medium) rs956792327 Functional Loss SNV dbSNP153 33..33 33 - - - 92900 RMVar_ID_92900 Human_SNP_ID_606677078 m1A Human chr16 + 67438475 67438445 67438475 GACCACATACACACACACGCACACACACGCGCACACACACACACACACACACAAAGAGTGCAATT GAC______________________________CACACACACACACACACACAAAGAGTGCAATT CCACATACACACACACGCACACACACGCGCA C NONHSAG019743.2 RNACentral:URS00009BC955 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67438425..67438502 26863196 MeRIP-seq:(Medium) rs1265758032 Functional Loss DEL dbSNP153 4..33 33 - - - 92901 RMVar_ID_92901 Human_SNP_ID_606677115 m1A Human chr16 + 67438475 67438475 67438475 GACCACATACACACACACGCACACACACGCGCACACACACACACACACACACAAAGAGTGCAATT GACCACATACACACACACGCACACACACGCGCGCACACACACACACACACACAAAGAGTGCAATT A G NONHSAG019743.2 RNACentral:URS00009BC955 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67438425..67438502 26863196 MeRIP-seq:(Medium) rs72650133 Functional Loss SNV dbSNP153 33..33 33 - - - 92902 RMVar_ID_92902 Human_SNP_ID_606677402 m1A Human chr16 + 67439255 67439255 67439255 CAGGCCAGGGCTAGCGGGCACCAGCAGGCAGGAGGGCGGGCAGGCACTCACCTCCAGGATGGGGC CAGGCCAGGGCTAGCGGGCACCAGCAGGCAGGGGGGCGGGCAGGCACTCACCTCCAGGATGGGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:67439251..67439375 32194978 MeRIP-seq:(Medium) rs1222129888 Functional Loss SNV dbSNP153 33..33 33 - - - 92903 RMVar_ID_92903 Human_SNP_ID_606679773 m1A Human chr16 - 67449598 67449580 67449598 GGTGGCTGGAGAAGAGGCAGCTGTCTGGCATGAGGCAGCTGTCTGGCATGGGGCCGACAGCCTGA GGTGGCTGGAGAAGAGGCAGCTGTCTGGCATG__________________GGGCCGACAGCCTGA CCATGCCAGACAGCTGCCT C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67449597..67449784 26863196 MeRIP-seq:(Medium) rs974857986 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_32849,RMVar_hsa_circ_85319,RMVar_hsa_circ_117044,RMVar_hsa_circ_179078,RMVar_hsa_circ_274091,RMVar_hsa_circ_179081,RMVar_hsa_circ_179082 92904 RMVar_ID_92904 Human_SNP_ID_606687084 m1A Human chr16 + 67481019 67481019 67481019 GGTAGTCGGCCTGGCTGAGCACCCCGGCCTTCAGGCCGCGCACCAGTCCCTCCAAGTAGCCATTG GGTAGTCGGCCTGGCTGAGCACCCCGGCCTTCCGGCCGCGCACCAGTCCCTCCAAGTAGCCATTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:67481001..67481025 32194978 MeRIP-seq:(Medium) rs1392421888 Functional Loss SNV dbSNP153 33..33 33 - - - 92905 RMVar_ID_92905 Human_SNP_ID_606687113 m1A Human chr16 + 67481099 67481099 67481099 AGCTCCGGGAAGAACGACATGGCTGCTGCGGGAGCGGCGGGACCGGAGAACCAGGACCGGCCGGC AGCTCCGGGAAGAACGACATGGCTGCTGCGGGGGCGGCGGGACCGGAGAACCAGGACCGGCCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67480900..67481150 26863196 MeRIP-seq:(Medium) rs757350377 Functional Loss SNV dbSNP153 33..33 33 - - - 92906 RMVar_ID_92906 Human_SNP_ID_606698009 m1A Human chr16 - 67524504 67524504 67524504 CCAGAAGGCAGCTGGACAGGCAGGGAGAAGAGAGAGGGGTCTGAGCTGGAGACATCTTCTGGGGG CCAGAAGGCAGCTGGACAGGCAGGGAGAAGAGGGAGGGGTCTGAGCTGGAGACATCTTCTGGGGG T C AC027682.6 Ensembl:ENSG00000276075 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67524497..67525061 26863196 MeRIP-seq:(Medium) rs1240511158 Functional Loss SNV dbSNP153 33..33 33 - - - 92907 RMVar_ID_92907 Human_SNP_ID_606699087 m1A Human chr16 + 67528909 67528909 67528909 AAGGACAGCGCGAGGTCCGCGCAGCCCAGCGCAGCCATGTGAGTGTCCCGCGCCGTTTCCGGGGC AAGGACAGCGCGAGGTCCGCGCAGCCCAGCGCGGCCATGTGAGTGTCCCGCGCCGTTTCCGGGGC A G RIPOR1 Ensembl:ENSG00000039523 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:67528860..67529064;chr16:67528860..67529036 26863196 MeRIP-seq:(Medium) rs1198874807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393915 Human_Splice_Rec_1727611,Human_Splice_Rec_1727653,Human_Splice_Rec_1727695,Human_Splice_Rec_1727709 92908 RMVar_ID_92908 Human_SNP_ID_606699089 m1A Human chr16 - 67528916 67528916 67528916 GCCTGCAGCCCCGGAAACGGCGCGGGACACTCACATGGCTGCGCTGGGCTGCGCGGACCTCGCGC GCCTGCAGCCCCGGAAACGGCGCGGGACACTCGCATGGCTGCGCTGGGCTGCGCGGACCTCGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:67528869..67528955;chr16:67528875..67529045 26863196 MeRIP-seq:(Medium) rs1276037658 Functional Loss SNV dbSNP153 33..33 33 - - - 92909 RMVar_ID_92909 Human_SNP_ID_606699406 m1A Human chr16 + 67530085 67530085 67530085 TGGGTCCTGTGACTGCGGCGGGAGAGAGGAGCAAGGTGAGCCGCCCCAGGGGTCTGGGTTTGGGT TGGGTCCTGTGACTGCGGCGGGAGAGAGGAGCGAGGTGAGCCGCCCCAGGGGTCTGGGTTTGGGT A G RIPOR1 Ensembl:ENSG00000039523 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67530076..67530171 26863196 MeRIP-seq:(Medium) rs1405285721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1727797 92910 RMVar_ID_92910 Human_SNP_ID_606699736 m1A Human chr16 - 67531528 67531528 67531528 AAGTCCCTCTCCTTCCTCAAGTCTACCCTATGACTTCTTCCTCCAGGAAGCAGGCCCTGGGTTGG AAGTCCCTCTCCTTCCTCAAGTCTACCCTATGGCTTCTTCCTCCAGGAAGCAGGCCCTGGGTTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67531527..67531710 26863196 MeRIP-seq:(Medium) rs950757501 Functional Loss SNV dbSNP153 33..33 33 - - - 92911 RMVar_ID_92911 Human_SNP_ID_606699758 m1A Human chr16 - 67531595 67531595 67531595 CAAGGTTCTTCAGAATCTGACCGGCAGCCCCCATCGCTCCTATTCCTTCTTCCCACTACTCAGCC CAAGGTTCTTCAGAATCTGACCGGCAGCCCCCGTCGCTCCTATTCCTTCTTCCCACTACTCAGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67530024..67537787 26863196 MeRIP-seq:(Medium) rs1346723962 Functional Loss SNV dbSNP153 33..33 33 - - - 92912 RMVar_ID_92912 Human_SNP_ID_606701110 m1A Human chr16 - 67537404 67537404 67537404 CCAGTTCCTGCCGCCTGACTCAGCCCGCCTGGATGGGGCGGGACCGGTGACTGGGGTTCCCCTCG CCAGTTCCTGCCGCCTGACTCAGCCCGCCTGGGTGGGGCGGGACCGGTGACTGGGGTTCCCCTCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67537399..67537756 26863196 MeRIP-seq:(Medium) rs990400194 Functional Loss SNV dbSNP153 33..33 33 - - - 92913 RMVar_ID_92913 Human_SNP_ID_606702085 m1A Human chr16 - 67540137 67540137 67540137 CAGGCTGTCCCGGGCCTCTCGGCTTCCCGGGGACCCAGTGGTGTAGGCACGGACCATGTTGTAGG CAGGCTGTCCCGGGCCTCTCGGCTTCCCGGGGGCCCAGTGGTGTAGGCACGGACCATGTTGTAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67540086..67540237 32194978 MeRIP-seq:(Medium) rs754994468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1727989 92914 RMVar_ID_92914 Human_SNP_ID_606702584 m1A Human chr16 + 67541696 67541696 67541696 AGGATGACCAGCCCTCAGCTGCTTCTTCTGTCAACAAGGCCTCCACAGTCACCAAGCGCTTCTCC AGGATGACCAGCCCTCAGCTGCTTCTTCTGTCCACAAGGCCTCCACAGTCACCAAGCGCTTCTCC A C RIPOR1 Ensembl:ENSG00000039523 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67541420..67541695 32194978 MeRIP-seq:(Medium) rs773878675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005048 Human_Splice_Rec_1727632,Human_Splice_Rec_1727633,Human_Splice_Rec_1727674,Human_Splice_Rec_1727675,Human_Splice_Rec_1727732,Human_Splice_Rec_1727733,Human_Splice_Rec_1727776,Human_Splice_Rec_1727777,Human_Splice_Rec_1727836,Human_Splice_Rec_1727837,Human_Splice_Rec_1727876,Human_Splice_Rec_1727877,Human_Splice_Rec_1727898,Human_Splice_Rec_1727899,Human_Splice_Rec_1727942,Human_Splice_Rec_1727954,Human_Splice_Rec_1727956,Human_Splice_Rec_1727957 RMVar_hsa_circ_95118,RMVar_hsa_circ_77250,RMVar_hsa_circ_179084,RMVar_hsa_circ_179085,RMVar_hsa_circ_87536,RMVar_hsa_circ_17766,RMVar_hsa_circ_75430,RMVar_hsa_circ_179086 92915 RMVar_ID_92915 Human_SNP_ID_606702814 m1A Human chr16 - 67542295 67542295 67542295 GAGCCTGTTGTACCGAGGGTAGAGCTTGTGGCAGAGTGGCCAGGGTCCAGGGCAGGAGGAACAGG GAGCCTGTTGTACCGAGGGTAGAGCTTGTGGCCGAGTGGCCAGGGTCCAGGGCAGGAGGAACAGG T G AC027682.2 Ensembl:ENSG00000259945 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:67542276..67542300 26863196 MeRIP-seq:(Medium) rs1184295166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5576352 Human_Splice_Rec_1727994 92916 RMVar_ID_92916 Human_SNP_ID_606702853 m1A Human chr16 + 67542440 67542440 67542440 TGCCAGGCCCCACTCACACCACTACAGGCTCTACCTATAGTGCCATTACCACTACCCACAGTGCT TGCCAGGCCCCACTCACACCACTACAGGCTCTGCCTATAGTGCCATTACCACTACCCACAGTGCT A G RIPOR1 Ensembl:ENSG00000039523 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:67542376..67542726 26863410 MeRIP-seq:(Medium) rs1317565868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45963 RMVar_hsa_circ_75430 92917 RMVar_ID_92917 Human_SNP_ID_606702883 m1A Human chr16 + 67542520 67542520 67542520 CACACTACTACAGGCTCCACCCACAAGCCCATAATCTCTACCCTTACTACTACAGGCCCTACCCT CACACTACTACAGGCTCCACCCACAAGCCCATCATCTCTACCCTTACTACTACAGGCCCTACCCT A C RIPOR1 Ensembl:ENSG00000039523 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:67542476..67542550 26863196 MeRIP-seq:(Medium) rs1174316235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128671,Human_RBP_ID_17254959,Human_RBP_ID_17371775,Human_RBP_ID_17487238,Human_RBP_ID_17879343,Human_RBP_ID_27444106 RMVar_hsa_circ_75430 92918 RMVar_ID_92918 Human_SNP_ID_606702885 m1A Human chr16 - 67542526 67542526 67542526 ATATTGAGGGTAGGGCCTGTAGTAGTAAGGGTAGAGATTATGGGCTTGTGGGTGGAGCCTGTAGT ATATTGAGGGTAGGGCCTGTAGTAGTAAGGGTGGAGATTATGGGCTTGTGGGTGGAGCCTGTAGT T C AC027682.3,AC027682.2 Ensembl:ENSG00000260894,Ensembl:ENSG00000259945 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67542188..67543035 26863196 MeRIP-seq:(Medium) rs778816969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1727995 92919 RMVar_ID_92919 Human_SNP_ID_606702893 m1A Human chr16 - 67542547 67542547 67542547 GTAGTCTGGACTGGGCCTATGATATTGAGGGTAGGGCCTGTAGTAGTAAGGGTAGAGATTATGGG GTAGTCTGGACTGGGCCTATGATATTGAGGGTGGGGCCTGTAGTAGTAAGGGTAGAGATTATGGG T C AC027682.3,AC027682.2 Ensembl:ENSG00000260894,Ensembl:ENSG00000259945 lincRNA,lincRNA exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:67542526..67542550 26863196 MeRIP-seq:(Medium) rs998037069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1727995 92920 RMVar_ID_92920 Human_SNP_ID_606703269 m1A Human chr16 + 67543488 67543488 67543488 GTTCCTGGGGACAGGTGAGGGGGCTAGGCAAGATGGGTGTGAGGCTAGGTGAGAGGGAAAAGGTG GTTCCTGGGGACAGGTGAGGGGGCTAGGCAAGTTGGGTGTGAGGCTAGGTGAGAGGGAAAAGGTG A T RIPOR1 Ensembl:ENSG00000039523 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67543482..67543585 26863196 MeRIP-seq:(Medium) rs1187428808 Functional Loss SNV dbSNP153 33..33 33 - - - 92921 RMVar_ID_92921 Human_SNP_ID_606703275 m1A Human chr16 - 67543495 67543495 67543495 CCTGCCTCACCTTTTCCCTCTCACCTAGCCTCACACCCATCTTGCCTAGCCCCCTCACCTGTCCC CCTGCCTCACCTTTTCCCTCTCACCTAGCCTCTCACCCATCTTGCCTAGCCCCCTCACCTGTCCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67543493..67543577 26863196 MeRIP-seq:(Medium) rs760145131 Functional Loss SNV dbSNP153 33..33 33 - - - 92922 RMVar_ID_92922 Human_SNP_ID_606708263 m1A Human chr16 + 67562615 67562615 67562615 TAAACCGTGCGCGGAGCTGCTTCTTTGGCGGCAGCGGCGGCGGCGGTGGCCGGTGCGGACGCGCG TAAACCGTGCGCGGAGCTGCTTCTTTGGCGGCGGCGGCGGCGGCGGTGGCCGGTGCGGACGCGCG A G CTCF Ensembl:ENSG00000102974 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:67562576..67571225;chr16:67562474..67610983;chr16:67562526..67611030 26863196 MeRIP-seq:(Medium) rs867414433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4377674,Human_RBP_ID_5316684,Human_RBP_ID_5465330,Human_RBP_ID_8812395,Human_RBP_ID_8941357,Human_RBP_ID_9285821,Human_RBP_ID_9325165,Human_RBP_ID_18418756,Human_RBP_ID_22944667,Human_RBP_ID_27811895 RMVar_hsa_circ_104522,RMVar_hsa_circ_179087 92923 RMVar_ID_92923 Human_SNP_ID_606708310 m1A Human chr16 + 67562723 67562723 67562723 GCGGAGCGGGCGCCGCGGGGGGTGTGGCGCGGAGGTAAGGGGGCCCGGGGTGGAGGAGGTTTCGC GCGGAGCGGGCGCCGCGGGGGGTGTGGCGCGGCGGTAAGGGGGCCCGGGGTGGAGGAGGTTTCGC A C CTCF Ensembl:ENSG00000102974 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67562551..67610993 26863196 MeRIP-seq:(Medium) rs1447872334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818164,Human_RBP_ID_4394890,Human_RBP_ID_8812395,Human_RBP_ID_8941357,Human_RBP_ID_9286347,Human_RBP_ID_18418756,Human_RBP_ID_22944667,Human_RBP_ID_27811895 Human_Splice_Rec_1727999,Human_Splice_Rec_1728023,Human_Splice_Rec_1728025,Human_Splice_Rec_1728047,Human_Splice_Rec_1728065 RMVar_hsa_circ_104522,RMVar_hsa_circ_179087 92924 RMVar_ID_92924 Human_SNP_ID_606708312 m1A Human chr16 - 67562726 67562726 67562726 CCCGCGAAACCTCCTCCACCCCGGGCCCCCTTACCTCCGCGCCACACCCCCCGCGGCGCCCGCTC CCCGCGAAACCTCCTCCACCCCGGGCCCCCTTCCCTCCGCGCCACACCCCCCGCGGCGCCCGCTC T G AC027682.4 Ensembl:ENSG00000261386 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:67562593..67562725 26863196 MeRIP-seq:(Medium) rs1014308429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3504597 92925 RMVar_ID_92925 Human_SNP_ID_606730703 m1A Human chr16 + 67636814 67636814 67636814 GCCCCACCACCCGCCAAGAAGCGGAGAGGACGACCCCCTGGCAGAACCAACCAGCCCAAACAGAA GCCCCACCACCCGCCAAGAAGCGGAGAGGACGCCCCCCTGGCAGAACCAACCAGCCCAAACAGAA A C CTCF Ensembl:ENSG00000102974 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67629447..67637804 26863196 MeRIP-seq:(Medium) rs772451262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6527044,Human_RBP_ID_26330173 Human_Splice_Rec_1728021,Human_Splice_Rec_1728045,Human_Splice_Rec_1728063,Human_Splice_Rec_1728085,Human_Splice_Rec_1728111,Human_Splice_Rec_1728131,Human_Splice_Rec_1728153,Human_Splice_Rec_1728177,Human_Splice_Rec_1728195,Human_Splice_Rec_1728217,Human_Splice_Rec_1728231,Human_Splice_Rec_1728241,Human_Splice_Rec_1728249 RMVar_hsa_circ_310170,RMVar_hsa_circ_268048,RMVar_hsa_circ_179108,RMVar_hsa_circ_372892 92926 RMVar_ID_92926 Human_SNP_ID_606730704 m1A Human chr16 + 67636814 67636814 67636814 GCCCCACCACCCGCCAAGAAGCGGAGAGGACGACCCCCTGGCAGAACCAACCAGCCCAAACAGAA GCCCCACCACCCGCCAAGAAGCGGAGAGGACGGCCCCCTGGCAGAACCAACCAGCCCAAACAGAA A G CTCF Ensembl:ENSG00000102974 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67629447..67637804 26863196 MeRIP-seq:(Medium) rs772451262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6527044,Human_RBP_ID_26330173 Human_Splice_Rec_1728021,Human_Splice_Rec_1728045,Human_Splice_Rec_1728063,Human_Splice_Rec_1728085,Human_Splice_Rec_1728111,Human_Splice_Rec_1728131,Human_Splice_Rec_1728153,Human_Splice_Rec_1728177,Human_Splice_Rec_1728195,Human_Splice_Rec_1728217,Human_Splice_Rec_1728231,Human_Splice_Rec_1728241,Human_Splice_Rec_1728249 RMVar_hsa_circ_310170,RMVar_hsa_circ_268048,RMVar_hsa_circ_179108,RMVar_hsa_circ_372892 92927 RMVar_ID_92927 Human_SNP_ID_606736962 m1A Human chr16 - 67654902 67654898 67654902 CCTCTCACTTCATGCTCAGGTCCCCTCAACTCACTTGCTTCCTCTTGCCTTCGGCACCCCCGCTG CCTCTCACTTCATGCTCAGGTCCCCTCAACTC____GCTTCCTCTTGCCTTCGGCACCCCCGCTG CAAGT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67654794..67656830 32194978 MeRIP-seq:(Medium) rs1457511046 Functional Loss DEL dbSNP153 33..36 33 - - - 92928 RMVar_ID_92928 Human_SNP_ID_606738091 m1A Human chr16 - 67658197 67658170 67658197 AGCCCCTGCCACCCTGACCCCCAGGTCCCCACACGCCAGCCGTACCCCCAGCTCCCCACTCCAGA AGCCCCTGCCACCCTGACCCCCAGGTCCCCAC___________________________TCCAGA AGTGGGGAGCTGGGGGTACGGCTGGCGT A ACD Ensembl:ENSG00000102977 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67658085..67658284 26863196 MeRIP-seq:(Medium) rs1198502930 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_234666,Human_RBP_ID_17077559,Human_RBP_ID_17257177,Human_RBP_ID_17371504,Human_RBP_ID_18939255 Human_miRNA_ID_1418466 92929 RMVar_ID_92929 Human_SNP_ID_606738916 m1A Human chr16 - 67660029 67660029 67660029 CGCTCGCCGCCGTCAGGTACTACAGGACGCCGAGGCCGCGGTCGCGGGCCCATCCCACGCCCCTG CGCTCGCCGCCGTCAGGTACTACAGGACGCCGGGGCCGCGGTCGCGGGCCCATCCCACGCCCCTG T C ACD Ensembl:ENSG00000102977 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67659983..67660220 26863196 MeRIP-seq:(Medium) rs745789392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234668,Human_RBP_ID_4393918 Human_Splice_Rec_1728488,Human_Splice_Rec_1728510,Human_Splice_Rec_1728532,Human_Splice_Rec_1728572,Human_Splice_Rec_1728594,Human_Splice_Rec_1728638 92930 RMVar_ID_92930 Human_SNP_ID_606740558 m1A Human chr16 + 67663973 67663973 67663973 GCTTCGGGACCTGGTGGGGTTGGCTGGGGACTAGATACATGGGGTGGTGGGAGGCCAGGGCCGCA GCTTCGGGACCTGGTGGGGTTGGCTGGGGACTCGATACATGGGGTGGTGGGAGGCCAGGGCCGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67663963..67664048 26863196 MeRIP-seq:(Medium) rs1411340696 Functional Loss SNV dbSNP153 33..33 33 - - - 92931 RMVar_ID_92931 Human_SNP_ID_606740597 m1A Human chr16 + 67664051 67664051 67664051 CGCAGGAAGTGGGCAGACTCTGTCCCAGAGGCAGGGCCAGGCTCCTGGAGGGCAGGGCACAGCAG CGCAGGAAGTGGGCAGACTCTGTCCCAGAGGCCGGGCCAGGCTCCTGGAGGGCAGGGCACAGCAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67662994..67664080 32194978 MeRIP-seq:(Medium) rs1443235543 Functional Loss SNV dbSNP153 33..33 33 - - - 92932 RMVar_ID_92932 Human_SNP_ID_606741135 m1A Human chr16 + 67666080 67666080 67666080 CTTCTTCCATTCCTGGGACTTACTCTTGAGAGAGGCCCCAGGACCTAGGGAGATCCCCTCGAGTT CTTCTTCCATTCCTGGGACTTACTCTTGAGAGTGGCCCCAGGACCTAGGGAGATCCCCTCGAGTT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67665001..67666448 32194978 MeRIP-seq:(Medium) rs763639292 Functional Loss SNV dbSNP153 33..33 33 - - - 92933 RMVar_ID_92933 Human_SNP_ID_606743711 m1A Human chr16 + 67675235 67675235 67675235 GGGCTCCTCCGTCAGCACCTCCACAGCCTCCCACTCCCCGGATCGGCTCGACCTCTTGATGGCAT GGGCTCCTCCGTCAGCACCTCCACAGCCTCCCTCTCCCCGGATCGGCTCGACCTCTTGATGGCAT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67674630..67676026 32194978 MeRIP-seq:(Medium) rs1327899809 Functional Loss SNV dbSNP153 33..33 33 - - - 92934 RMVar_ID_92934 Human_SNP_ID_606746264 m1A Human chr16 + 67685461 67685461 67685461 TGCCCCTGCTGTGGCCTGCCGGGCGTACCTAGAGCCTTCACGGATATCTGCCGGGTGAGTGGAGG TGCCCCTGCTGTGGCCTGCCGGGCGTACCTAGTGCCTTCACGGATATCTGCCGGGTGAGTGGAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67685412..67685513 32194978 MeRIP-seq:(Medium) rs746731186 Functional Loss SNV dbSNP153 33..33 33 - - - 92935 RMVar_ID_92935 Human_SNP_ID_606746329 m1A Human chr16 + 67685634 67685634 67685634 CTCAGTCTTCCCCCACAGGGCCTCAACAGTGAACCCTTCTGCCCTCAGCAGTGGGACCAGAACTC CTCAGTCTTCCCCCACAGGGCCTCAACAGTGACCCCTTCTGCCCTCAGCAGTGGGACCAGAACTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67685585..67719315 26863196 MeRIP-seq:(Medium) rs1213162168 Functional Loss SNV dbSNP153 33..33 33 - - - 92936 RMVar_ID_92936 Human_SNP_ID_606746330 m1A Human chr16 + 67685634 67685634 67685634 CTCAGTCTTCCCCCACAGGGCCTCAACAGTGAACCCTTCTGCCCTCAGCAGTGGGACCAGAACTC CTCAGTCTTCCCCCACAGGGCCTCAACAGTGATCCCTTCTGCCCTCAGCAGTGGGACCAGAACTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67685585..67719315 26863196 MeRIP-seq:(Medium) rs1213162168 Functional Loss SNV dbSNP153 33..33 33 - - - 92937 RMVar_ID_92937 Human_SNP_ID_606746381 m1A Human chr16 + 67685796 67685796 67685796 TGGATATGATCTTCCAAACGTCCTGGTCAGACATGGCTCCTAGAATAGCAAACATTACACTGGTT TGGATATGATCTTCCAAACGTCCTGGTCAGACGTGGCTCCTAGAATAGCAAACATTACACTGGTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67685761..67719271 32194978 MeRIP-seq:(Medium) rs978897060 Functional Loss SNV dbSNP153 33..33 33 - - - 92938 RMVar_ID_92938 Human_SNP_ID_606757063 m1A Human chr16 - 67729728 67729728 67729728 CCAAGTCCCAGGACAGCTACCCTGGCTCCCCCAGCCTCAGTCCCCGACATGGCCCCAGTAGTTCC CCAAGTCCCAGGACAGCTACCCTGGCTCCCCCGGCCTCAGTCCCCGACATGGCCCCAGTAGTTCC T C RANBP10 Ensembl:ENSG00000141084 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67729647..67729778 26863196 MeRIP-seq:(Medium) rs760273026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1728769,Human_Splice_Rec_1728791,Human_Splice_Rec_1728815,Human_Splice_Rec_1728847,Human_Splice_Rec_1728873 Human_miRNA_ID_2685555,Human_miRNA_ID_2715679,Human_miRNA_ID_3051661 RMVar_hsa_circ_695,RMVar_hsa_circ_336505,RMVar_hsa_circ_366567,RMVar_hsa_circ_344840,RMVar_hsa_circ_179116 92939 RMVar_ID_92939 Human_SNP_ID_606782751 m1A Human chr16 + 67829488 67829487 67829489 AACTGATGATGTCGCCTGGCCTGGAGAGACTCAGGGGTGCTGGAGGCCGACTCTGGACTTGCTAC AACTGATGATGTCGCCTGGCCTGGAGAGACTC__GGGTGCTGGAGGCCGACTCTGGACTTGCTAC CAG C TSNAXIP1 Ensembl:ENSG00000102904 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67829165..67829866 32194978 MeRIP-seq:(Medium) rs753595432 Functional Loss DEL dbSNP153 33..34 33 - - - 92940 RMVar_ID_92940 Human_SNP_ID_606782870 m1A Human chr16 - 67829875 67829875 67829875 GGCAACAGGAGCACAAGGACCCAGCAGGGTAGAAGAGGCTGAGGGACACACAGAGGTGACAGAAG GGCAACAGGAGCACAAGGACCCAGCAGGGTAGCAGAGGCTGAGGGACACACAGAGGTGACAGAAG T G CENPT Ensembl:ENSG00000102901 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67829826..67830023 26863196 MeRIP-seq:(Medium) rs1345413002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760769,Human_RBP_ID_892331,Human_RBP_ID_3947796,Human_RBP_ID_5114296,Human_RBP_ID_9372973,Human_RBP_ID_18983972,Human_RBP_ID_22415506,Human_RBP_ID_22944461,Human_RBP_ID_26328171 RMVar_hsa_circ_179127,RMVar_hsa_circ_110378,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128,RMVar_hsa_circ_179126 92941 RMVar_ID_92941 Human_SNP_ID_606782892 m1A Human chr16 + 67829941 67829941 67829941 CCATTTCACTCACACTCACACCTTCTTCTTCCATCTTTTTCTCTGCCTCTTCAACTCCATCGTGT CCATTTCACTCACACTCACACCTTCTTCTTCCGTCTTTTTCTCTGCCTCTTCAACTCCATCGTGT A G TSNAXIP1 Ensembl:ENSG00000102904 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67829753..67830075 26863196 MeRIP-seq:(Medium) rs546308121 Functional Loss SNV dbSNP153 33..33 33 - - - 92942 RMVar_ID_92942 Human_SNP_ID_606783046 m1A Human chr16 - 67830353 67830353 67830353 GTGTGTGGCACTGGTGGCCTGGAGCCAAATTTAGCTTGGGTGAGAGTTGACAATGGTAGTTTTCC GTGTGTGGCACTGGTGGCCTGGAGCCAAATTTGGCTTGGGTGAGAGTTGACAATGGTAGTTTTCC T C CENPT Ensembl:ENSG00000102901 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67830214..67830464 32194978 MeRIP-seq:(Medium) rs1287354338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44026,Human_RBP_ID_888837,Human_RBP_ID_1844890,Human_RBP_ID_3947797,Human_RBP_ID_12778861,Human_RBP_ID_18983975,Human_RBP_ID_19071827,Human_RBP_ID_22415507,Human_RBP_ID_23696247 RMVar_hsa_circ_179127,RMVar_hsa_circ_110378,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128,RMVar_hsa_circ_179126 92943 RMVar_ID_92943 Human_SNP_ID_606783599 m1A Human chr16 - 67832030 67832028 67832030 GCCAGCACCGCAGGCGGTCCAACCCTCCAGACAAGAGAGCAGTTGCGGCAGGTACACAGAACTCC GCCAGCACCGCAGGCGGTCCAACCCTCCAGAC__GAGAGCAGTTGCGGCAGGTACACAGAACTCC CTT C CENPT Ensembl:ENSG00000102901 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67831561..67832099 32194978 MeRIP-seq:(Medium) rs771666658 Functional Loss DEL dbSNP153,HGVD 33..34 33 - - - Human_RBP_ID_233326,Human_RBP_ID_3949369,Human_RBP_ID_9372979,Human_RBP_ID_18986600,Human_RBP_ID_26329113 Human_Splice_Rec_1729184,Human_Splice_Rec_1729185,Human_Splice_Rec_1729210,Human_Splice_Rec_1729211,Human_Splice_Rec_1729234,Human_Splice_Rec_1729235,Human_Splice_Rec_1729258,Human_Splice_Rec_1729259,Human_Splice_Rec_1729278,Human_Splice_Rec_1729279,Human_Splice_Rec_1729302,Human_Splice_Rec_1729303,Human_Splice_Rec_1729324,Human_Splice_Rec_1729325,Human_Splice_Rec_1729358,Human_Splice_Rec_1729359,Human_Splice_Rec_1729380,Human_Splice_Rec_1729381,Human_Splice_Rec_1729404,Human_Splice_Rec_1729405,Human_Splice_Rec_1729413,Human_Splice_Rec_1729416,Human_Splice_Rec_1729417,Human_Splice_Rec_1729428,Human_Splice_Rec_1729429,Human_Splice_Rec_1729440,Human_Splice_Rec_1729441,Human_Splice_Rec_1729450,Human_Splice_Rec_1729451,Human_Splice_Rec_1729458,Human_Splice_Rec_1729459,Human_Splice_Rec_1729468,Human_Splice_Rec_1729469,Human_Splice_Rec_1729477,Human_Splice_Rec_1729483 RMVar_hsa_circ_179127,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128,RMVar_hsa_circ_179129,RMVar_hsa_circ_374012 92944 RMVar_ID_92944 Human_SNP_ID_606783602 m1A Human chr16 - 67832030 67832030 67832030 GCCAGCACCGCAGGCGGTCCAACCCTCCAGACAAGAGAGCAGTTGCGGCAGGTACACAGAACTCC GCCAGCACCGCAGGCGGTCCAACCCTCCAGACGAGAGAGCAGTTGCGGCAGGTACACAGAACTCC T C CENPT Ensembl:ENSG00000102901 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67831561..67832099 32194978 MeRIP-seq:(Medium) rs759013748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233326,Human_RBP_ID_3949369,Human_RBP_ID_9372979,Human_RBP_ID_18986600,Human_RBP_ID_26329113 Human_Splice_Rec_1729184,Human_Splice_Rec_1729185,Human_Splice_Rec_1729210,Human_Splice_Rec_1729211,Human_Splice_Rec_1729234,Human_Splice_Rec_1729235,Human_Splice_Rec_1729258,Human_Splice_Rec_1729259,Human_Splice_Rec_1729278,Human_Splice_Rec_1729279,Human_Splice_Rec_1729302,Human_Splice_Rec_1729303,Human_Splice_Rec_1729324,Human_Splice_Rec_1729325,Human_Splice_Rec_1729358,Human_Splice_Rec_1729359,Human_Splice_Rec_1729380,Human_Splice_Rec_1729381,Human_Splice_Rec_1729404,Human_Splice_Rec_1729405,Human_Splice_Rec_1729413,Human_Splice_Rec_1729416,Human_Splice_Rec_1729417,Human_Splice_Rec_1729428,Human_Splice_Rec_1729429,Human_Splice_Rec_1729440,Human_Splice_Rec_1729441,Human_Splice_Rec_1729450,Human_Splice_Rec_1729451,Human_Splice_Rec_1729458,Human_Splice_Rec_1729459,Human_Splice_Rec_1729468,Human_Splice_Rec_1729469,Human_Splice_Rec_1729477,Human_Splice_Rec_1729483 RMVar_hsa_circ_179127,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128,RMVar_hsa_circ_179129,RMVar_hsa_circ_374012 92945 RMVar_ID_92945 Human_SNP_ID_606783603 m1A Human chr16 - 67832030 67832030 67832030 GCCAGCACCGCAGGCGGTCCAACCCTCCAGACAAGAGAGCAGTTGCGGCAGGTACACAGAACTCC GCCAGCACCGCAGGCGGTCCAACCCTCCAGACCAGAGAGCAGTTGCGGCAGGTACACAGAACTCC T G CENPT Ensembl:ENSG00000102901 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67831561..67832099 32194978 MeRIP-seq:(Medium) rs759013748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233326,Human_RBP_ID_3949369,Human_RBP_ID_9372979,Human_RBP_ID_18986600,Human_RBP_ID_26329113 Human_Splice_Rec_1729184,Human_Splice_Rec_1729185,Human_Splice_Rec_1729210,Human_Splice_Rec_1729211,Human_Splice_Rec_1729234,Human_Splice_Rec_1729235,Human_Splice_Rec_1729258,Human_Splice_Rec_1729259,Human_Splice_Rec_1729278,Human_Splice_Rec_1729279,Human_Splice_Rec_1729302,Human_Splice_Rec_1729303,Human_Splice_Rec_1729324,Human_Splice_Rec_1729325,Human_Splice_Rec_1729358,Human_Splice_Rec_1729359,Human_Splice_Rec_1729380,Human_Splice_Rec_1729381,Human_Splice_Rec_1729404,Human_Splice_Rec_1729405,Human_Splice_Rec_1729413,Human_Splice_Rec_1729416,Human_Splice_Rec_1729417,Human_Splice_Rec_1729428,Human_Splice_Rec_1729429,Human_Splice_Rec_1729440,Human_Splice_Rec_1729441,Human_Splice_Rec_1729450,Human_Splice_Rec_1729451,Human_Splice_Rec_1729458,Human_Splice_Rec_1729459,Human_Splice_Rec_1729468,Human_Splice_Rec_1729469,Human_Splice_Rec_1729477,Human_Splice_Rec_1729483 RMVar_hsa_circ_179127,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128,RMVar_hsa_circ_179129,RMVar_hsa_circ_374012 92946 RMVar_ID_92946 Human_SNP_ID_606784149 m1A Human chr16 - 67833834 67833834 67833834 CGAGACGATGGCTGACCACAACCCTGACAGCGACTCCACGCCGCGCACGCTGCTGCGACGCGTGC CGAGACGATGGCTGACCACAACCCTGACAGCGTCTCCACGCCGCGCACGCTGCTGCGACGCGTGC T A CENPT Ensembl:ENSG00000102901 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:67833751..67833900;chr16:67833784..67833900 26863196 MeRIP-seq:(Medium) rs772159728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5832,Human_RBP_ID_1282801,Human_RBP_ID_4378042,Human_RBP_ID_9372983,Human_RBP_ID_18419399,Human_RBP_ID_18986603,Human_RBP_ID_22944670 Human_Splice_Rec_1729181,Human_Splice_Rec_1729205,Human_Splice_Rec_1729229,Human_Splice_Rec_1729253,Human_Splice_Rec_1729273,Human_Splice_Rec_1729297,Human_Splice_Rec_1729321,Human_Splice_Rec_1729353,Human_Splice_Rec_1729375,Human_Splice_Rec_1729399,Human_Splice_Rec_1729411,Human_Splice_Rec_1729425,Human_Splice_Rec_1729435,Human_Splice_Rec_1729447,Human_Splice_Rec_1729453,Human_Splice_Rec_1729463,Human_Splice_Rec_1729471,Human_Splice_Rec_1729479,Human_Splice_Rec_1729487,Human_Splice_Rec_1729493,Human_Splice_Rec_1729499 RMVar_hsa_circ_179127,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128 92947 RMVar_ID_92947 Human_SNP_ID_606784152 m1A Human chr16 - 67833838 67833838 67833838 GGGCCGAGACGATGGCTGACCACAACCCTGACAGCGACTCCACGCCGCGCACGCTGCTGCGACGC GGGCCGAGACGATGGCTGACCACAACCCTGACGGCGACTCCACGCCGCGCACGCTGCTGCGACGC T C CENPT Ensembl:ENSG00000102901 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67832530..67833900 26863196 MeRIP-seq:(Medium) rs766145204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5832,Human_RBP_ID_1282801,Human_RBP_ID_4378044,Human_RBP_ID_9372983,Human_RBP_ID_18419399,Human_RBP_ID_18682246,Human_RBP_ID_18986603,Human_RBP_ID_22944670 Human_Splice_Rec_1729181,Human_Splice_Rec_1729205,Human_Splice_Rec_1729229,Human_Splice_Rec_1729253,Human_Splice_Rec_1729273,Human_Splice_Rec_1729297,Human_Splice_Rec_1729321,Human_Splice_Rec_1729353,Human_Splice_Rec_1729375,Human_Splice_Rec_1729399,Human_Splice_Rec_1729411,Human_Splice_Rec_1729425,Human_Splice_Rec_1729435,Human_Splice_Rec_1729447,Human_Splice_Rec_1729453,Human_Splice_Rec_1729463,Human_Splice_Rec_1729471,Human_Splice_Rec_1729479,Human_Splice_Rec_1729487,Human_Splice_Rec_1729493,Human_Splice_Rec_1729499 RMVar_hsa_circ_179127,RMVar_hsa_circ_120506,RMVar_hsa_circ_85892,RMVar_hsa_circ_179128 92948 RMVar_ID_92948 Human_SNP_ID_606786670 m1A Human chr16 + 67842347 67842347 67842347 TCCCCGGGGCCCACTCCCGAGCGCAGGCGGGCAGCCAGGCGGGCGGCGCGGCGCGGGCCGGCAGG TCCCCGGGGCCCACTCCCGAGCGCAGGCGGGCGGCCAGGCGGGCGGCGCGGCGCGGGCCGGCAGG A G THAP11 Ensembl:ENSG00000168286 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67842293..67842860 26863196 MeRIP-seq:(Medium) rs995943560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235056,Human_RBP_ID_4393186 92949 RMVar_ID_92949 Human_SNP_ID_606786817 m1A Human chr16 + 67842722 67842722 67842722 AGTGGGTGCTTCTCCACCTTCCAGCCCACCACAGGCCACCGTCTCTGCAGCGTTCACTTCCAGGG AGTGGGTGCTTCTCCACCTTCCAGCCCACCACCGGCCACCGTCTCTGCAGCGTTCACTTCCAGGG A C THAP11 Ensembl:ENSG00000168286 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67842474..67842721 32194978 MeRIP-seq:(Medium) rs1193733631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5259425,Human_RBP_ID_26810465,Human_RBP_ID_27444211 92950 RMVar_ID_92950 Human_SNP_ID_606787115 m1A Human chr16 - 67843010 67843010 67843010 GTGGCCTGAAGGGTGAGAAGCACGGCCGCGGAAGCAGATACCAGGTTCGGCTGCAGCTGGGCAGT GTGGCCTGAAGGGTGAGAAGCACGGCCGCGGAGGCAGATACCAGGTTCGGCTGCAGCTGGGCAGT T C CENPT Ensembl:ENSG00000102901 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67842961..67843117 26863196 MeRIP-seq:(Medium) rs1355660965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1729501,Human_Splice_Rec_1729511,Human_Splice_Rec_1729517,Human_Splice_Rec_1729535,Human_Splice_Rec_1729545 92951 RMVar_ID_92951 Human_SNP_ID_606788382 m1A Human chr16 + 67847212 67847212 67847212 GGGGTAACGCACAGAGAGCCAGCCGGGCGCCTATCTGGGCCGTACCGTGCTGGTGGCTGGTGCAC GGGGTAACGCACAGAGAGCCAGCCGGGCGCCTCTCTGGGCCGTACCGTGCTGGTGGCTGGTGCAC A C NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:67847188..67847425 26863196 MeRIP-seq:(Medium) rs1299962548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4378160 92952 RMVar_ID_92952 Human_SNP_ID_606793786 m1A Human chr16 + 67868423 67868423 67868423 GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGAAGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGAGGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC A G NUTF2 Ensembl:ENSG00000102898 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67868420..67868519 26863196 MeRIP-seq:(Medium) rs2271294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12779553,Human_RBP_ID_19074777,Human_RBP_ID_23696275 Human_Splice_Rec_1729562,Human_Splice_Rec_1729566,Human_Splice_Rec_1729574,Human_Splice_Rec_1729582,Human_Splice_Rec_1729590,Human_Splice_Rec_1729598,Human_Splice_Rec_1729606 GWAS_ID_12115,GWAS_ID_12116,GWAS_ID_12117,GWAS_ID_12118,GWAS_ID_12119,GWAS_ID_12120 RMVar_hsa_circ_84061,RMVar_hsa_circ_283198,RMVar_hsa_circ_179132,RMVar_hsa_circ_292199,RMVar_hsa_circ_179133 92953 RMVar_ID_92953 Human_SNP_ID_606793787 m1A Human chr16 + 67868423 67868423 67868423 GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGAAGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGATGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC A T NUTF2 Ensembl:ENSG00000102898 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67868420..67868519 26863196 MeRIP-seq:(Medium) rs2271294 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_12779553,Human_RBP_ID_19074777,Human_RBP_ID_23696275 Human_Splice_Rec_1729562,Human_Splice_Rec_1729566,Human_Splice_Rec_1729574,Human_Splice_Rec_1729582,Human_Splice_Rec_1729590,Human_Splice_Rec_1729598,Human_Splice_Rec_1729606 GWAS_ID_12115,GWAS_ID_12116,GWAS_ID_12117,GWAS_ID_12118,GWAS_ID_12119,GWAS_ID_12120 RMVar_hsa_circ_84061,RMVar_hsa_circ_283198,RMVar_hsa_circ_179132,RMVar_hsa_circ_292199,RMVar_hsa_circ_179133 92954 RMVar_ID_92954 Human_SNP_ID_606794967 m1A Human chr16 - 67873200 67873200 67873200 CGCGTTCGTTCCGCCGCCGCCGCGCACCACGCACCCTCGCTCACCCGCCACGGGGCGAGACAGCG CGCGTTCGTTCCGCCGCCGCCGCGCACCACGCGCCCTCGCTCACCCGCCACGGGGCGAGACAGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:67873151..67873289 26863196 MeRIP-seq:(Medium) rs935794023 Functional Loss SNV dbSNP153 33..33 33 - - - 92955 RMVar_ID_92955 Human_SNP_ID_606794968 m1A Human chr16 - 67873200 67873200 67873200 CGCGTTCGTTCCGCCGCCGCCGCGCACCACGCACCCTCGCTCACCCGCCACGGGGCGAGACAGCG CGCGTTCGTTCCGCCGCCGCCGCGCACCACGCCCCCTCGCTCACCCGCCACGGGGCGAGACAGCG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:67873151..67873289 26863196 MeRIP-seq:(Medium) rs935794023 Functional Loss SNV dbSNP153 33..33 33 - - - 92956 RMVar_ID_92956 Human_SNP_ID_606796798 m1A Human chr16 - 67879711 67879711 67879711 GCGTCAGGTGTCATCAACTTGGGCTTGGTCTCACTGCTCAGACTGAGGAAGTCGGCAGGTGCAGG GCGTCAGGTGTCATCAACTTGGGCTTGGTCTCCCTGCTCAGACTGAGGAAGTCGGCAGGTGCAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67879661..67879766 26863196 MeRIP-seq:(Medium) rs1253020749 Functional Loss SNV dbSNP153 33..33 33 - - - 92957 RMVar_ID_92957 Human_SNP_ID_606797585 m1A Human chr16 + 67881840 67881840 67881840 CGTAGAACGTGCCCTTGAGACTCGGCACGAGCAGGAACGTATCCTTGAGACTGGTAGCACAACAT CGTAGAACGTGCCCTTGAGACTCGGCACGAGCCGGAACGTATCCTTGAGACTGGTAGCACAACAT A C EDC4 Ensembl:ENSG00000038358 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67881657..67881855 26863196 MeRIP-seq:(Medium) rs774789553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12779795,Human_RBP_ID_23209676 Human_Splice_Rec_1729647,Human_Splice_Rec_1729703,Human_Splice_Rec_1729801 RMVar_hsa_circ_121355,RMVar_hsa_circ_89720,RMVar_hsa_circ_279737,RMVar_hsa_circ_179138,RMVar_hsa_circ_179139,RMVar_hsa_circ_179141,RMVar_hsa_circ_85775,RMVar_hsa_circ_87191,RMVar_hsa_circ_179144,RMVar_hsa_circ_82857,RMVar_hsa_circ_179147,RMVar_hsa_circ_315196,RMVar_hsa_circ_179149 92958 RMVar_ID_92958 Human_SNP_ID_606797677 m1A Human chr16 + 67882048 67882048 67882048 CTGACACAACAGTTGTCCCAAGCACTGTCGTCAGCTGTAGCTGGGCGGCTAGAGCGCAGCATACG CTGACACAACAGTTGTCCCAAGCACTGTCGTCGGCTGTAGCTGGGCGGCTAGAGCGCAGCATACG A G EDC4 Ensembl:ENSG00000038358 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67881917..67882049 26863196 MeRIP-seq:(Medium) rs1567391734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477794,Human_RBP_ID_1520781,Human_RBP_ID_6527527,Human_RBP_ID_8809225,Human_RBP_ID_9285183,Human_RBP_ID_22941007,Human_RBP_ID_23209394 Human_Splice_Rec_1729648,Human_Splice_Rec_1729649,Human_Splice_Rec_1729704,Human_Splice_Rec_1729705,Human_Splice_Rec_1729802,Human_Splice_Rec_1729803,Human_Splice_Rec_1729839,Human_Splice_Rec_1729843 Human_miRNA_ID_3010839 RMVar_hsa_circ_121355,RMVar_hsa_circ_89720,RMVar_hsa_circ_179138,RMVar_hsa_circ_179141,RMVar_hsa_circ_85775,RMVar_hsa_circ_87191,RMVar_hsa_circ_179144,RMVar_hsa_circ_82857,RMVar_hsa_circ_179147,RMVar_hsa_circ_179149 92959 RMVar_ID_92959 Human_SNP_ID_606798007 m1A Human chr16 + 67883055 67883055 67883055 AGGAGCAGCAGGCCGCCGTCACCTCCAGCATCATGCAGGCCATGCGCTCAGCTGCTGGCACACCT AGGAGCAGCAGGCCGCCGTCACCTCCAGCATCGTGCAGGCCATGCGCTCAGCTGCTGGCACACCT A G AC040162.3,EDC4 Ensembl:ENSG00000263126,Ensembl:ENSG00000038358 lincRNA,Protein coding exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67883004..67883203 32194978 MeRIP-seq:(Medium) rs1234411552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510294,Human_RBP_ID_8811994,Human_RBP_ID_22801993,Human_RBP_ID_27444268 Human_Splice_Rec_1729656,Human_Splice_Rec_1729712,Human_Splice_Rec_1729810,Human_Splice_Rec_1729856 RMVar_hsa_circ_121355,RMVar_hsa_circ_179138,RMVar_hsa_circ_21606,RMVar_hsa_circ_82857,RMVar_hsa_circ_179149,RMVar_hsa_circ_99042,RMVar_hsa_circ_25207,RMVar_hsa_circ_179150 92960 RMVar_ID_92960 Human_SNP_ID_606810454 m1A Human chr16 - 67931459 67931458 67931459 AACTGTTCAGGTCGGGAGGGGGCAGAGAGACCAGGGGTAGAGATGGGGAACAGCGGGGACTAGGC AACTGTTCAGGTCGGGAGGGGGCAGAGAGACC_GGGGTAGAGATGGGGAACAGCGGGGACTAGGC CT C AC040162.1,CTRL Ensembl:ENSG00000261884,Ensembl:ENSG00000141086 Protein coding,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67931410..67931691 26863196 MeRIP-seq:(Medium) rs1306449325 Functional Loss DEL dbSNP153 33..33 33 - - - 92961 RMVar_ID_92961 Human_SNP_ID_606811309 m1A Human chr16 - 67934600 67934600 67934600 CCTGACCCAGACAGTGAAGCCACTAACCCTGGAGCTAGTGGAGGAAACTGTGCAGGCTATGGAGG CCTGACCCAGACAGTGAAGCCACTAACCCTGGCGCTAGTGGAGGAAACTGTGCAGGCTATGGAGG T G AC040162.1,PSMB10 Ensembl:ENSG00000261884,Ensembl:ENSG00000205220 Protein coding,Protein coding exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:67934550..67934799;chr16:67934550..67936076 32194978 MeRIP-seq:(Medium) rs750557294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_477838 Human_Splice_Rec_1729938,Human_Splice_Rec_1729948,Human_Splice_Rec_1729949,Human_Splice_Rec_1729956,Human_Splice_Rec_1729964,Human_Splice_Rec_1729978 92962 RMVar_ID_92962 Human_SNP_ID_606814648 m1A Human chr16 - 67944810 67944810 67944810 TGAGCCCAGTGTCATCTTGTGGCCTGGAGTCGAGGTCTTGGCCAGGACATAACAAGCTGTGGTCT TGAGCCCAGTGTCATCTTGTGGCCTGGAGTCGCGGTCTTGGCCAGGACATAACAAGCTGTGGTCT T G SLC12A4 Ensembl:ENSG00000124067 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67944423..67944923 32194978 MeRIP-seq:(Medium) rs1323430313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373000,Human_RBP_ID_18190055,Human_RBP_ID_18984016 Human_miRNA_ID_1347413 RMVar_hsa_circ_179157,RMVar_hsa_circ_81413 92963 RMVar_ID_92963 Human_SNP_ID_606814953 m1A Human chr16 + 67945488 67945488 67945488 ATCTGGATCTTGTCAGCCCCCACTGCAGACTCATCTTCCTCGTCCGAGTACAGGCTCTCCAGCCG ATCTGGATCTTGTCAGCCCCCACTGCAGACTCGTCTTCCTCGTCCGAGTACAGGCTCTCCAGCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67945372..67945523 32194978 MeRIP-seq:(Medium) rs1487060864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12780141 92964 RMVar_ID_92964 Human_SNP_ID_606815229 m1A Human chr16 - 67946250 67946250 67946250 CTTCTACCCCAGCAACCACGAGCGCTACCTGGAGGGCCACATAGACGTGTGGTGGATCGTGCACG CTTCTACCCCAGCAACCACGAGCGCTACCTGGTGGGCCACATAGACGTGTGGTGGATCGTGCACG T A SLC12A4 Ensembl:ENSG00000124067 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67946199..67947425 32194978 MeRIP-seq:(Medium) rs1224594991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892356,Human_RBP_ID_4378491 Human_Splice_Rec_1730078,Human_Splice_Rec_1730079,Human_Splice_Rec_1730122,Human_Splice_Rec_1730123,Human_Splice_Rec_1730166,Human_Splice_Rec_1730167,Human_Splice_Rec_1730212,Human_Splice_Rec_1730213,Human_Splice_Rec_1730258,Human_Splice_Rec_1730259,Human_Splice_Rec_1730302,Human_Splice_Rec_1730303,Human_Splice_Rec_1730346,Human_Splice_Rec_1730347,Human_Splice_Rec_1730362,Human_Splice_Rec_1730363 Human_miRNA_ID_2427527 RMVar_hsa_circ_179157,RMVar_hsa_circ_81413,RMVar_hsa_circ_294199,RMVar_hsa_circ_179159,RMVar_hsa_circ_82820,RMVar_hsa_circ_91485,RMVar_hsa_circ_114980,RMVar_hsa_circ_179160,RMVar_hsa_circ_179158 92965 RMVar_ID_92965 Human_SNP_ID_606816890 m1A Human chr16 - 67951218 67951218 67951218 TGCCCTCCGCAGATGCCCCGAGCCTGAAGGAGAGCCTGCCTCTGTACGTGGTCGCTGACATCGCC TGCCCTCCGCAGATGCCCCGAGCCTGAAGGAGCGCCTGCCTCTGTACGTGGTCGCTGACATCGCC T G SLC12A4 Ensembl:ENSG00000124067 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67951167..67951318 32194978 MeRIP-seq:(Medium) rs752852592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18411696,Human_RBP_ID_18984038,Human_RBP_ID_23209682,Human_RBP_ID_27811191 Human_Splice_Rec_1730058,Human_Splice_Rec_1730059,Human_Splice_Rec_1730102,Human_Splice_Rec_1730103,Human_Splice_Rec_1730146,Human_Splice_Rec_1730147,Human_Splice_Rec_1730192,Human_Splice_Rec_1730193,Human_Splice_Rec_1730238,Human_Splice_Rec_1730239,Human_Splice_Rec_1730282,Human_Splice_Rec_1730283,Human_Splice_Rec_1730326,Human_Splice_Rec_1730327,Human_Splice_Rec_1730384,Human_Splice_Rec_1730385,Human_Splice_Rec_1730403,Human_Splice_Rec_1730411,Human_Splice_Rec_1730416,Human_Splice_Rec_1730426,Human_Splice_Rec_1730427 RMVar_hsa_circ_179157,RMVar_hsa_circ_81413,RMVar_hsa_circ_117186,RMVar_hsa_circ_82820,RMVar_hsa_circ_179160,RMVar_hsa_circ_348877,RMVar_hsa_circ_179163,RMVar_hsa_circ_343082,RMVar_hsa_circ_37076,RMVar_hsa_circ_100266,RMVar_hsa_circ_90752,RMVar_hsa_circ_179165,RMVar_hsa_circ_375773,RMVar_hsa_circ_179168,RMVar_hsa_circ_179169,RMVar_hsa_circ_62795,RMVar_hsa_circ_22674 92966 RMVar_ID_92966 Human_SNP_ID_606819611 m1A Human chr16 - 67961615 67961615 67961615 CAACCTCACCCAGGGCGCCAAAGAGCATGAGGAGGCCGAGAGTGGGGAGGGCACCCGCCGGAGGG CAACCTCACCCAGGGCGCCAAAGAGCATGAGGTGGCCGAGAGTGGGGAGGGCACCCGCCGGAGGG T A SLC12A4 Ensembl:ENSG00000124067 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67957908..67961639 32194978 MeRIP-seq:(Medium) rs1462407514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892379,Human_RBP_ID_3949411,Human_RBP_ID_18469785,Human_RBP_ID_18986688,Human_RBP_ID_19071886,Human_RBP_ID_27811192 Human_Splice_Rec_1730046,Human_Splice_Rec_1730047,Human_Splice_Rec_1730090,Human_Splice_Rec_1730091,Human_Splice_Rec_1730134,Human_Splice_Rec_1730135,Human_Splice_Rec_1730180,Human_Splice_Rec_1730181,Human_Splice_Rec_1730226,Human_Splice_Rec_1730227,Human_Splice_Rec_1730270,Human_Splice_Rec_1730271,Human_Splice_Rec_1730314,Human_Splice_Rec_1730315,Human_Splice_Rec_1730372,Human_Splice_Rec_1730373,Human_Splice_Rec_1730432,Human_Splice_Rec_1730433,Human_Splice_Rec_1730444,Human_Splice_Rec_1730445,Human_Splice_Rec_1730456,Human_Splice_Rec_1730457 RMVar_hsa_circ_3043,RMVar_hsa_circ_100266,RMVar_hsa_circ_375773,RMVar_hsa_circ_179168,RMVar_hsa_circ_179169,RMVar_hsa_circ_124440,RMVar_hsa_circ_68777,RMVar_hsa_circ_94391,RMVar_hsa_circ_179171,RMVar_hsa_circ_179172,RMVar_hsa_circ_291870 92967 RMVar_ID_92967 Human_SNP_ID_606819612 m1A Human chr16 - 67961615 67961615 67961615 CAACCTCACCCAGGGCGCCAAAGAGCATGAGGAGGCCGAGAGTGGGGAGGGCACCCGCCGGAGGG CAACCTCACCCAGGGCGCCAAAGAGCATGAGGGGGCCGAGAGTGGGGAGGGCACCCGCCGGAGGG T C SLC12A4 Ensembl:ENSG00000124067 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67957908..67961639 32194978 MeRIP-seq:(Medium) rs1462407514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892379,Human_RBP_ID_3949411,Human_RBP_ID_18469785,Human_RBP_ID_18986688,Human_RBP_ID_19071886,Human_RBP_ID_27811192 Human_Splice_Rec_1730046,Human_Splice_Rec_1730047,Human_Splice_Rec_1730090,Human_Splice_Rec_1730091,Human_Splice_Rec_1730134,Human_Splice_Rec_1730135,Human_Splice_Rec_1730180,Human_Splice_Rec_1730181,Human_Splice_Rec_1730226,Human_Splice_Rec_1730227,Human_Splice_Rec_1730270,Human_Splice_Rec_1730271,Human_Splice_Rec_1730314,Human_Splice_Rec_1730315,Human_Splice_Rec_1730372,Human_Splice_Rec_1730373,Human_Splice_Rec_1730432,Human_Splice_Rec_1730433,Human_Splice_Rec_1730444,Human_Splice_Rec_1730445,Human_Splice_Rec_1730456,Human_Splice_Rec_1730457 RMVar_hsa_circ_3043,RMVar_hsa_circ_100266,RMVar_hsa_circ_375773,RMVar_hsa_circ_179168,RMVar_hsa_circ_179169,RMVar_hsa_circ_124440,RMVar_hsa_circ_68777,RMVar_hsa_circ_94391,RMVar_hsa_circ_179171,RMVar_hsa_circ_179172,RMVar_hsa_circ_291870 92968 RMVar_ID_92968 Human_SNP_ID_606821392 m1A Human chr16 - 67968525 67968525 67968525 CACGATGCCTCACTTCACCGTGGTGCCAGTGGACGGGCCGAGGCGCGGCGACTATGACAACCTCG CACGATGCCTCACTTCACCGTGGTGCCAGTGGGCGGGCCGAGGCGCGGCGACTATGACAACCTCG T C SLC12A4 Ensembl:ENSG00000124067 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67968442..67968543 32194978 MeRIP-seq:(Medium) rs540888852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947847,Human_RBP_ID_8941358,Human_RBP_ID_9326034,Human_RBP_ID_18190532,Human_RBP_ID_18418759,Human_RBP_ID_26329129,Human_RBP_ID_27444321 Human_Splice_Rec_1730043,Human_Splice_Rec_1730089,Human_Splice_Rec_1730133,Human_Splice_Rec_1730223,Human_Splice_Rec_1730267,Human_Splice_Rec_1730369,Human_Splice_Rec_1730421,Human_Splice_Rec_1730453 Human_miRNA_ID_1967385,Human_miRNA_ID_2969435 RMVar_hsa_circ_124440,RMVar_hsa_circ_179172 92969 RMVar_ID_92969 Human_SNP_ID_606821415 m1A Human chr16 + 67968588 67968570 67968588 TGCGGGCTCGGCCCCGCCGCACCCGCCGTCCCAGCCGCCCGCCGCTGTCCCCGCCGCTGTCCCCG TGCGGGCTCGGCCCC__________________GCCGCCCGCCGCTGTCCCCGCCGCTGTCCCCG CGCCGCACCCGCCGTCCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67968397..67968650 26863196 MeRIP-seq:(Medium) rs1355888262 Functional Loss DEL dbSNP153 16..33 33 - - - 92970 RMVar_ID_92970 Human_SNP_ID_606821420 m1A Human chr16 + 67968576 67968576 67968576 AGTGAGGCATCGTGCGGGCTCGGCCCCGCCGCACCCGCCGTCCCAGCCGCCCGCCGCTGTCCCCG AGTGAGGCATCGTGCGGGCTCGGCCCCGCCGCCCCCGCCGTCCCAGCCGCCCGCCGCTGTCCCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67968381..67968629 26863196 MeRIP-seq:(Medium) rs1005691479 Functional Loss SNV dbSNP153 33..33 33 - - - 92971 RMVar_ID_92971 Human_SNP_ID_606821423 m1A Human chr16 - 67968584 67968582 67968584 GACAGCGGCGGGGACAGCGGCGGGCGGCTGGGACGGCGGGTGCGGCGGGGCCGAGCCCGCACGAT GACAGCGGCGGGGACAGCGGCGGGCGGCTGGG__GGCGGGTGCGGCGGGGCCGAGCCCGCACGAT CGT C SLC12A4 Ensembl:ENSG00000124067 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:67968385..67968625;chr16:67968390..67968625 26863196 MeRIP-seq:(Medium) rs1555502917 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_233577,Human_RBP_ID_761196,Human_RBP_ID_818025,Human_RBP_ID_3502752,Human_RBP_ID_5236630,Human_RBP_ID_5316689,Human_RBP_ID_9325172,Human_RBP_ID_18418759,Human_RBP_ID_26329129 RMVar_hsa_circ_124440,RMVar_hsa_circ_179172 92972 RMVar_ID_92972 Human_SNP_ID_606821425 m1A Human chr16 - 67968584 67968584 67968584 GACAGCGGCGGGGACAGCGGCGGGCGGCTGGGACGGCGGGTGCGGCGGGGCCGAGCCCGCACGAT GACAGCGGCGGGGACAGCGGCGGGCGGCTGGGTCGGCGGGTGCGGCGGGGCCGAGCCCGCACGAT T A SLC12A4 Ensembl:ENSG00000124067 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:67968385..67968625;chr16:67968390..67968625 26863196 MeRIP-seq:(Medium) rs1193243618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233577,Human_RBP_ID_761196,Human_RBP_ID_818025,Human_RBP_ID_3502752,Human_RBP_ID_5236630,Human_RBP_ID_5316689,Human_RBP_ID_9325172,Human_RBP_ID_18418759,Human_RBP_ID_26329129 RMVar_hsa_circ_124440,RMVar_hsa_circ_179172 92973 RMVar_ID_92973 Human_SNP_ID_606821426 m1A Human chr16 + 67968588 67968587 67968589 TGCGGGCTCGGCCCCGCCGCACCCGCCGTCCCAGCCGCCCGCCGCTGTCCCCGCCGCTGTCCCCG TGCGGGCTCGGCCCCGCCGCACCCGCCGTCCC__CCGCCCGCCGCTGTCCCCGCCGCTGTCCCCG CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67968397..67968650 26863196 MeRIP-seq:(Medium) rs1555502920 Functional Loss DEL dbSNP153 33..34 33 - - - 92974 RMVar_ID_92974 Human_SNP_ID_606841469 m1A Human chr16 + 68039815 68039815 68039815 AAAATTAGACCCCTGGAGGACAGCTCTAGCACATAGACATGAACACTCACGGAGTTAATGGCTTG AAAATTAGACCCCTGGAGGACAGCTCTAGCACGTAGACATGAACACTCACGGAGTTAATGGCTTG A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68039800..68039865 26863196 MeRIP-seq:(Medium) rs1429153310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28772,RMVar_hsa_circ_47122,RMVar_hsa_circ_99498,RMVar_hsa_circ_330428,RMVar_hsa_circ_179175,RMVar_hsa_circ_87968,RMVar_hsa_circ_360853,RMVar_hsa_circ_179174,RMVar_hsa_circ_332664,RMVar_hsa_circ_280695,RMVar_hsa_circ_271056,RMVar_hsa_circ_179177,RMVar_hsa_circ_179176,RMVar_hsa_circ_358257,RMVar_hsa_circ_325614,RMVar_hsa_circ_333138,RMVar_hsa_circ_305238,RMVar_hsa_circ_179180,RMVar_hsa_circ_179181,RMVar_hsa_circ_179182 92975 RMVar_ID_92975 Human_SNP_ID_606854932 m1A Human chr16 + 68095764 68095764 68095764 GTCAGAGTCCTTGGGGATGGGCATGGGAGTTGATAGAGGTGCCAAGAAAGAGAAGTATGGCTATT GTCAGAGTCCTTGGGGATGGGCATGGGAGTTGGTAGAGGTGCCAAGAAAGAGAAGTATGGCTATT A G AC130462.3,NFATC3 Ensembl:ENSG00000261864,Ensembl:ENSG00000072736 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68095758..68095875 26863196 MeRIP-seq:(Medium) rs139953767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80319,RMVar_hsa_circ_179197 92976 RMVar_ID_92976 Human_SNP_ID_606855180 m1A Human chr16 + 68097020 68097020 68097020 GGAGGTGGGGACACATGTATTTGAGAAATGATAAGGGTAGAGCAGTGAAGACGACAAAGTGGGAA GGAGGTGGGGACACATGTATTTGAGAAATGATGAGGGTAGAGCAGTGAAGACGACAAAGTGGGAA A G AC130462.3,NFATC3 Ensembl:ENSG00000261864,Ensembl:ENSG00000072736 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:68097011..68097107 26863196 MeRIP-seq:(Medium) rs1219358973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12780886 RMVar_hsa_circ_80319,RMVar_hsa_circ_179197 92977 RMVar_ID_92977 Human_SNP_ID_606889741 m1A Human chr16 - 68232689 68232689 68232689 ATAGCTCTGACAGCACTGTGCCCTGCCCCTACAGCAGCAAGGCTGATGTGGTGGACAGTGAGACT ATAGCTCTGACAGCACTGTGCCCTGCCCCTACTGCAGCAAGGCTGATGTGGTGGACAGTGAGACT T A ESRP2 Ensembl:ENSG00000103067 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:68232567..68232736;chr16:68232657..68232749 26863196 MeRIP-seq:(Medium) rs1025909942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892391,Human_RBP_ID_5358377,Human_RBP_ID_18984071,Human_RBP_ID_19074846,Human_RBP_ID_22541730,Human_RBP_ID_22738883,Human_RBP_ID_26780544 Human_Splice_Rec_1731194 RMVar_hsa_circ_179222,RMVar_hsa_circ_127536 92978 RMVar_ID_92978 Human_SNP_ID_606890791 m1A Human chr16 + 68235938 68235938 68235938 GAGCCCAGGTCCCGTCCCAGCGCACCCGCCGTAGCCCCGAAGAGGACGACCAGTGATCCGGGCCA GAGCCCAGGTCCCGTCCCAGCGCACCCGCCGTGGCCCCGAAGAGGACGACCAGTGATCCGGGCCA A G L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:68235901..68236100 26863196 MeRIP-seq:(Medium) rs763517082 Functional Loss SNV dbSNP153 33..33 33 - - - 92979 RMVar_ID_92979 Human_SNP_ID_606890819 m1A Human chr16 - 68235993 68235993 68235993 GCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGACCCCGCCGCGGACCCCTGCCCCTGGCCCGGAT GCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGCCCCCGCCGCGGACCCCTGCCCCTGGCCCGGAT T G ESRP2 Ensembl:ENSG00000103067 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:68235837..68236100 26863196 MeRIP-seq:(Medium) rs1018552761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4378844,Human_RBP_ID_18419077 92980 RMVar_ID_92980 Human_SNP_ID_606890826 m1A Human chr16 + 68236019 68236007 68236020 GCGGGGTCGGCCGCGGGGTCAGGGCCCGGGGGAGGGGGCGGCGGCGGCGGCGGAGTCATGGCCGC GCGGGGTCGGCCGCGGGGTCA_____________GGGGCGGCGGCGGCGGCGGAGTCATGGCCGC AGGGCCCGGGGGAG A L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68235979..68236091 26863196 MeRIP-seq:(Medium) rs767961739 Functional Loss DEL dbSNP153 22..34 33 - - - 92981 RMVar_ID_92981 Human_SNP_ID_606890832 m1A Human chr16 + 68236019 68236019 68236019 GCGGGGTCGGCCGCGGGGTCAGGGCCCGGGGGAGGGGGCGGCGGCGGCGGCGGAGTCATGGCCGC GCGGGGTCGGCCGCGGGGTCAGGGCCCGGGGGGGGGGGCGGCGGCGGCGGCGGAGTCATGGCCGC A G L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68235979..68236091 26863196 MeRIP-seq:(Medium) rs997886751 Functional Loss SNV dbSNP153 33..33 33 - - - 92982 RMVar_ID_92982 Human_SNP_ID_606898196 m1A Human chr16 - 68264253 68264253 68264253 CCTGGAGTTAGATGGGGCCTCCGAGGGCGTCCACAGCGGACATTCCCGCGGGGAGCTCTCATCGG CCTGGAGTTAGATGGGGCCTCCGAGGGCGTCCGCAGCGGACATTCCCGCGGGGAGCTCTCATCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68264222..68264423 26863196 MeRIP-seq:(Medium) rs1198081128 Functional Loss SNV dbSNP153 33..33 33 - - - 92983 RMVar_ID_92983 Human_SNP_ID_606900663 m1A Human chr16 + 68274784 68274784 68274784 CCACACCCACCTACCATCTTGTCCCTAACACCAGCCAGTCCCAGGTGGAAGAAGATGTCAGCTCG CCACACCCACCTACCATCTTGTCCCTAACACCGGCCAGTCCCAGGTGGAAGAAGATGTCAGCTCG A G SLC7A6 Ensembl:ENSG00000103064 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68274733..68274800 26863196 MeRIP-seq:(Medium) rs773590135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44148,Human_RBP_ID_760833,Human_RBP_ID_894150,Human_RBP_ID_9373006 Human_Splice_Rec_1731382,Human_Splice_Rec_1731402,Human_Splice_Rec_1731426,Human_Splice_Rec_1731446,Human_Splice_Rec_1731468,Human_Splice_Rec_1731469,Human_Splice_Rec_1731478,Human_Splice_Rec_1731500,Human_Splice_Rec_1731504,Human_Splice_Rec_1731508,Human_Splice_Rec_1731510,Human_Splice_Rec_1731520,Human_Splice_Rec_1731524 RMVar_hsa_circ_179232,RMVar_hsa_circ_274079,RMVar_hsa_circ_88143,RMVar_hsa_circ_91429,RMVar_hsa_circ_315644,RMVar_hsa_circ_372976,RMVar_hsa_circ_179228,RMVar_hsa_circ_179229,RMVar_hsa_circ_375292,RMVar_hsa_circ_372263,RMVar_hsa_circ_354650,RMVar_hsa_circ_308580,RMVar_hsa_circ_314640,RMVar_hsa_circ_296067,RMVar_hsa_circ_179236,RMVar_hsa_circ_111783,RMVar_hsa_circ_179237,RMVar_hsa_circ_179234,RMVar_hsa_circ_179235,RMVar_hsa_circ_179233,RMVar_hsa_circ_179242,RMVar_hsa_circ_91249,RMVar_hsa_circ_179230,RMVar_hsa_circ_179231,RMVar_hsa_circ_111921,RMVar_hsa_circ_179240,RMVar_hsa_circ_179241,RMVar_hsa_circ_270345,RMVar_hsa_circ_289527,RMVar_hsa_circ_362625,RMVar_hsa_circ_179243 92984 RMVar_ID_92984 Human_SNP_ID_606908021 m1A Human chr16 - 68304045 68304045 68304045 CTGGATTGAGAACATCCTCTCCGTGCAGCCCTACAGCCAAGAATGGGAGCTGGTAAGGGGGCCCA CTGGATTGAGAACATCCTCTCCGTGCAGCCCTGCAGCCAAGAATGGGAGCTGGTAAGGGGGCCCA T C SLC7A6OS Ensembl:ENSG00000103061 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11548855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373009 Human_Splice_Rec_1731547,Human_Splice_Rec_1731555,Human_Splice_Rec_1731561,Human_Splice_Rec_1731565 RMVar_hsa_circ_42678,RMVar_hsa_circ_71250,RMVar_hsa_circ_179253 92985 RMVar_ID_92985 Human_SNP_ID_606910041 m1A Human chr16 - 68311101 68311101 68311101 CGACCCCACCTTCCCAGCATACCCAGCGCCTCACCCGCCGCGGGAAACCCTCCGCTCGCCTCCGC CGACCCCACCTTCCCAGCATACCCAGCGCCTCCCCCGCCGCGGGAAACCCTCCGCTCGCCTCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr16:68311074..68311177;chr16:68311079..68311183;chr16:68311077..68311182;chr16:68311078..68311162;chr16:68311073..68311223 26863196,32194978 MeRIP-seq:(Medium) rs890105071 Functional Loss SNV dbSNP153 33..33 33 - - - 92986 RMVar_ID_92986 Human_SNP_ID_606911492 m1A Human chr16 + 68316044 68316044 68316044 CACGGGGTCTGTGGAGTGGCTGGAGGAGGATGAACACTATGATTACCACCAGGAGATTGCAAGGT CACGGGGTCTGTGGAGTGGCTGGAGGAGGATGGACACTATGATTACCACCAGGAGATTGCAAGGT A G PRMT7 Ensembl:ENSG00000132600 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:68315901..68316044 26863196 MeRIP-seq:(Medium) rs910672785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393939,Human_RBP_ID_5571915,Human_RBP_ID_6528359,Human_RBP_ID_12783995,Human_RBP_ID_22944673 Human_Splice_Rec_1731575,Human_Splice_Rec_1731581,Human_Splice_Rec_1731593,Human_Splice_Rec_1731597,Human_Splice_Rec_1731609,Human_Splice_Rec_1731627,Human_Splice_Rec_1731639,Human_Splice_Rec_1731685,Human_Splice_Rec_1731705,Human_Splice_Rec_1731735,Human_Splice_Rec_1731767,Human_Splice_Rec_1731799,Human_Splice_Rec_1731805,Human_Splice_Rec_1731811,Human_Splice_Rec_1731843,Human_Splice_Rec_1731847 RMVar_hsa_circ_340373 92987 RMVar_ID_92987 Human_SNP_ID_606913929 m1A Human chr16 + 68324732 68324732 68324732 AGGTATCCGGGCTGCCGTGAGCAGGGTGAAGGACAGAGGACAGAAGGCCTTGGTTCTCGACATTG AGGTATCCGGGCTGCCGTGAGCAGGGTGAAGGGCAGAGGACAGAAGGCCTTGGTTCTCGACATTG A G PRMT7 Ensembl:ENSG00000132600 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:68324659..68324789 26863196 MeRIP-seq:(Medium) rs202175390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3949421,Human_RBP_ID_8811996,Human_RBP_ID_12784192,Human_RBP_ID_22945115 Human_Splice_Rec_1731578,Human_Splice_Rec_1731584,Human_Splice_Rec_1731596,Human_Splice_Rec_1731600,Human_Splice_Rec_1731610,Human_Splice_Rec_1731630,Human_Splice_Rec_1731674,Human_Splice_Rec_1731688,Human_Splice_Rec_1731706,Human_Splice_Rec_1731718,Human_Splice_Rec_1731738,Human_Splice_Rec_1731770,Human_Splice_Rec_1731802,Human_Splice_Rec_1731808,Human_Splice_Rec_1731814,Human_Splice_Rec_1731846 Human_miRNA_ID_1966419,Human_miRNA_ID_2361876,Human_miRNA_ID_2571174,Human_miRNA_ID_3044910 RMVar_hsa_circ_85592,RMVar_hsa_circ_280960,RMVar_hsa_circ_283871,RMVar_hsa_circ_340373,RMVar_hsa_circ_94598,RMVar_hsa_circ_96991,RMVar_hsa_circ_91222,RMVar_hsa_circ_179256,RMVar_hsa_circ_179258,RMVar_hsa_circ_179260,RMVar_hsa_circ_179261,RMVar_hsa_circ_179259,RMVar_hsa_circ_179257,RMVar_hsa_circ_42376,RMVar_hsa_circ_315918,RMVar_hsa_circ_358896,RMVar_hsa_circ_365158,RMVar_hsa_circ_118965,RMVar_hsa_circ_179262,RMVar_hsa_circ_179263 92988 RMVar_ID_92988 Human_SNP_ID_606914659 m1A Human chr16 + 68327481 68327481 68327481 GGGAAGTGGGGTTTGATTTGGCAGGTGGGGCCAGGATAGGGAAGGCTCAGTGATCATGAGATCAT GGGAAGTGGGGTTTGATTTGGCAGGTGGGGCCGGGATAGGGAAGGCTCAGTGATCATGAGATCAT A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:68327476..68327619 26863196 MeRIP-seq:(Medium) rs1344355984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233642,Human_RBP_ID_818681 RMVar_hsa_circ_85592,RMVar_hsa_circ_280960,RMVar_hsa_circ_340373,RMVar_hsa_circ_94598,RMVar_hsa_circ_96991,RMVar_hsa_circ_91222,RMVar_hsa_circ_179258,RMVar_hsa_circ_179260,RMVar_hsa_circ_179261,RMVar_hsa_circ_179259,RMVar_hsa_circ_179257,RMVar_hsa_circ_42376,RMVar_hsa_circ_315918,RMVar_hsa_circ_358896,RMVar_hsa_circ_365158,RMVar_hsa_circ_118965,RMVar_hsa_circ_179262,RMVar_hsa_circ_179263 92989 RMVar_ID_92989 Human_SNP_ID_606914664 m1A Human chr16 + 68327491 68327491 68327491 GTTTGATTTGGCAGGTGGGGCCAGGATAGGGAAGGCTCAGTGATCATGAGATCATTGTGGCTGGA GTTTGATTTGGCAGGTGGGGCCAGGATAGGGAGGGCTCAGTGATCATGAGATCATTGTGGCTGGA A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68327486..68327563 26863196 MeRIP-seq:(Medium) rs1372633635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233642,Human_RBP_ID_818681 RMVar_hsa_circ_85592,RMVar_hsa_circ_280960,RMVar_hsa_circ_340373,RMVar_hsa_circ_94598,RMVar_hsa_circ_96991,RMVar_hsa_circ_91222,RMVar_hsa_circ_179258,RMVar_hsa_circ_179260,RMVar_hsa_circ_179261,RMVar_hsa_circ_179259,RMVar_hsa_circ_179257,RMVar_hsa_circ_42376,RMVar_hsa_circ_315918,RMVar_hsa_circ_358896,RMVar_hsa_circ_365158,RMVar_hsa_circ_118965,RMVar_hsa_circ_179262,RMVar_hsa_circ_179263 92990 RMVar_ID_92990 Human_SNP_ID_606917544 m1A Human chr16 - 68338226 68338226 68338226 CAGGCCTCTGTCTACAGCCTTAGCTGAGGCCCACTGTACCACAGCGTCTGGACGATTCCACAGCC CAGGCCTCTGTCTACAGCCTTAGCTGAGGCCCGCTGTACCACAGCGTCTGGACGATTCCACAGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68338214..68338356 26863196 MeRIP-seq:(Medium) rs966636866 Functional Loss SNV dbSNP153 33..33 33 - - - 92991 RMVar_ID_92991 Human_SNP_ID_606917545 m1A Human chr16 - 68338226 68338226 68338226 CAGGCCTCTGTCTACAGCCTTAGCTGAGGCCCACTGTACCACAGCGTCTGGACGATTCCACAGCC CAGGCCTCTGTCTACAGCCTTAGCTGAGGCCCCCTGTACCACAGCGTCTGGACGATTCCACAGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68338214..68338356 26863196 MeRIP-seq:(Medium) rs966636866 Functional Loss SNV dbSNP153 33..33 33 - - - 92992 RMVar_ID_92992 Human_SNP_ID_606923157 m1A Human chr16 + 68357234 68357232 68357234 GGCATGCAGATACCCCAGACTGACCACTCTTGAGCAATAAAGTGGCCTGAGGGCTGGGGTTCTGA GGCATGCAGATACCCCAGACTGACCACTCTT__GCAATAAAGTGGCCTGAGGGCTGGGGTTCTGA TGA T PRMT7 Ensembl:ENSG00000132600 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:68357218..68357319 32194978 MeRIP-seq:(Medium) rs1203673253 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8437115,Human_RBP_ID_12784556 Human_miRNA_ID_268534 RMVar_hsa_circ_265528 92993 RMVar_ID_92993 Human_SNP_ID_606923372 m1A Human chr16 + 68357865 68357865 68357865 GGACCTGAGACTGGACACAAGGCAGCTGTCCCAGAGCAGTTCCTGAGATGCAGGCCCAGGAAAGT GGACCTGAGACTGGACACAAGGCAGCTGTCCCGGAGCAGTTCCTGAGATGCAGGCCCAGGAAAGT A G PRMT7 Ensembl:ENSG00000132600 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:68357815..68358215 32194978 MeRIP-seq:(Medium) rs578154226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802015 92994 RMVar_ID_92994 Human_SNP_ID_606927113 m1A Human chr16 + 68368412 68368412 68368412 CCTGAGGCAGTGGAGGGCATAAGAGGAGTCACACCTGGCCTCAGACGAGGAGGGTGGCTGAAACC CCTGAGGCAGTGGAGGGCATAAGAGGAGTCACCCCTGGCCTCAGACGAGGAGGGTGGCTGAAACC A C L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:68368365..68368494 26863196 MeRIP-seq:(Medium) rs1474537897 Functional Loss SNV dbSNP153 33..33 33 - - - 92995 RMVar_ID_92995 Human_SNP_ID_606966109 m1A Human chr16 + 68530289 68530289 68530289 CCCTGCAACTAGCCTGCCGCTTCCCTCCCGGCACCCCCGCCGCCAGCCCCGAGCGCGGACCTGGA CCCTGCAACTAGCCTGCCGCTTCCCTCCCGGCCCCCCCGCCGCCAGCCCCGAGCGCGGACCTGGA A C ZFP90 Ensembl:ENSG00000184939 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:68530189..68530307 26863196 MeRIP-seq:(Medium) rs879604104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1731975,Human_Splice_Rec_1731981 92996 RMVar_ID_92996 Human_SNP_ID_606969325 m1A Human chr16 + 68539455 68539455 68539455 GCTCTGGGTGGGCCGGAGGTCGCGAAATCCGGAGCCCCCCAGAGGCGGTGATTCTGAGTGCGCGG GCTCTGGGTGGGCCGGAGGTCGCGAAATCCGGGGCCCCCCAGAGGCGGTGATTCTGAGTGCGCGG A G ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68539366..68539486 26863196 MeRIP-seq:(Medium) rs1341142368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234225,Human_RBP_ID_22944878 Human_Splice_Rec_1731999,Human_Splice_Rec_1732007,Human_Splice_Rec_1732023,Human_Splice_Rec_1732031,Human_Splice_Rec_1732039,Human_Splice_Rec_1732045,Human_Splice_Rec_1732061,Human_Splice_Rec_1732069 RMVar_hsa_circ_99542,RMVar_hsa_circ_104884,RMVar_hsa_circ_179268,RMVar_hsa_circ_179269 92997 RMVar_ID_92997 Human_SNP_ID_606969503 m1A Human chr16 - 68539744 68539744 68539744 CCCGGCTCCGGGGCAGGAGCTGGGGAGAAAGGACAGGGCCCACTCACCCCGCTGCAACACCGACC CCCGGCTCCGGGGCAGGAGCTGGGGAGAAAGGGCAGGGCCCACTCACCCCGCTGCAACACCGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68539734..68539803 26863196 MeRIP-seq:(Medium) rs780498261 Functional Loss SNV dbSNP153 33..33 33 - - - 92998 RMVar_ID_92998 Human_SNP_ID_606969693 m1A Human chr16 + 68540082 68540082 68540082 AGGAGTTGAGATTGGATGCGTTGGGAAGTGTCAGTTTTGAGAGTCCTGAATGCCACGCCAGTTTT AGGAGTTGAGATTGGATGCGTTGGGAAGTGTCGGTTTTGAGAGTCCTGAATGCCACGCCAGTTTT A G ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68540056..68540333 26863196 MeRIP-seq:(Medium) rs1362181849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12784672 RMVar_hsa_circ_105731,RMVar_hsa_circ_99542,RMVar_hsa_circ_104884,RMVar_hsa_circ_179268,RMVar_hsa_circ_179269,RMVar_hsa_circ_283768,RMVar_hsa_circ_179271,RMVar_hsa_circ_40734,RMVar_hsa_circ_179272,RMVar_hsa_circ_179270 92999 RMVar_ID_92999 Human_SNP_ID_606973835 m1A Human chr16 + 68553969 68553951 68553969 TTAACAAGATCTCTCTGGTTGTAATGTGGAAAATGGACTTGGGTGGTGGGGCAAGAGTGAGAGGA TTAACAAGATCTCTC__________________TGGACTTGGGTGGTGGGGCAAGAGTGAGAGGA CTGGTTGTAATGTGGAAAA C ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68553946..68554052 26863196 MeRIP-seq:(Medium) rs1246338753 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_23696879 RMVar_hsa_circ_105731,RMVar_hsa_circ_99542,RMVar_hsa_circ_104884,RMVar_hsa_circ_179268,RMVar_hsa_circ_179269,RMVar_hsa_circ_283768,RMVar_hsa_circ_179271,RMVar_hsa_circ_40734,RMVar_hsa_circ_179272,RMVar_hsa_circ_179270 93000 RMVar_ID_93000 Human_SNP_ID_606997560 m1A Human chr16 - 68645346 68645346 68645346 GCTGCAGAGAGAGGGGTGAAGCAGCTGCCGCGACGGCGGGCCGGTGTTCCGCTCAGCTCTTGCCC GCTGCAGAGAGAGGGGTGAAGCAGCTGCCGCGGCGGCGGGCCGGTGTTCCGCTCAGCTCTTGCCC T C AC126773.4 Ensembl:ENSG00000260577 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68645300..68645428 26863196 MeRIP-seq:(Medium) rs1414633544 Functional Loss SNV dbSNP153 33..33 33 - - - 93001 RMVar_ID_93001 Human_SNP_ID_606997855 m1A Human chr16 - 68646000 68646000 68646000 TCGAGACTGGGTGAGGGGCTCAGCCATCCGGCATCTCGGAGGAGGGGGTCAAGGTAAGCAGTGGC TCGAGACTGGGTGAGGGGCTCAGCCATCCGGCGTCTCGGAGGAGGGGGTCAAGGTAAGCAGTGGC T C AC126773.4 Ensembl:ENSG00000260577 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68645993..68646235 26863196 MeRIP-seq:(Medium) rs191016948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1732209 93002 RMVar_ID_93002 Human_SNP_ID_607051615 m1A Human chr16 - 68843616 68843616 68843616 CCCCGCTGCCCACGGCCTGTCGGGCCGCCATGACTGGAGTGTAACACCACGCTCGCGACCCGCTC CCCCGCTGCCCACGGCCTGTCGGGCCGCCATGTCTGGAGTGTAACACCACGCTCGCGACCCGCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:68843573..68843692 26863196 MeRIP-seq:(Medium) rs1482074639 Functional Loss SNV dbSNP153 33..33 33 - - - 93003 RMVar_ID_93003 Human_SNP_ID_607106034 m1A Human chr16 + 69072081 69072068 69072081 GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGACCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GTGTGTGTGTGTGTGTGTGT_____________CCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG TAGAGAGAGGGAGA T TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69072075..69072147 26863196 MeRIP-seq:(Medium) rs1409482826 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_5288694,Human_RBP_ID_5646890,Human_RBP_ID_23696985 RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 93004 RMVar_ID_93004 Human_SNP_ID_607106048 m1A Human chr16 + 69072081 69072074 69072082 GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGACCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GTGTGTGTGTGTGTGTGTGTAGAGAG________CGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GAGGGAGAC G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69072075..69072147 26863196 MeRIP-seq:(Medium) rs1567570618 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_5288694,Human_RBP_ID_5646890,Human_RBP_ID_23696985 RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 93005 RMVar_ID_93005 Human_SNP_ID_607106052 m1A Human chr16 + 69072081 69072076 69072082 GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGACCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GTGTGTGTGTGTGTGTGTGTAGAGAGAG______CGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GGGAGAC G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69072075..69072147 26863196 MeRIP-seq:(Medium) rs1200324772 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_5288694,Human_RBP_ID_5646890,Human_RBP_ID_23696985 RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 93006 RMVar_ID_93006 Human_SNP_ID_607106054 m1A Human chr16 + 69072081 69072078 69072082 GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGACCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GTGTGTGTGTGTGTGTGTGTAGAGAGAGGG____CGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GAGAC G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69072075..69072147 26863196 MeRIP-seq:(Medium) rs1475940672 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5288694,Human_RBP_ID_5646890,Human_RBP_ID_23696985 RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 93007 RMVar_ID_93007 Human_SNP_ID_607106055 m1A Human chr16 + 69072081 69072081 69072081 GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGACCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG GTGTGTGTGTGTGTGTGTGTAGAGAGAGGGAGGCCGTGTGTGTGTGTGTGTATGTGTGAAGAGAG A G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69072075..69072147 26863196 MeRIP-seq:(Medium) rs1567570621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5288694,Human_RBP_ID_5646890,Human_RBP_ID_23696985 RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 93008 RMVar_ID_93008 Human_SNP_ID_607119236 m1A Human chr16 - 69121126 69121126 69121126 AGGCCTGGCAGAATGGGTGCTGATGGAGCTACAGGGGGAGATCGAGGCTCGCTACAGCACTGGAT AGGCCTGGCAGAATGGGTGCTGATGGAGCTACCGGGGGAGATCGAGGCTCGCTACAGCACTGGAT T G DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69121076..69121217 26863196 MeRIP-seq:(Medium) rs1026353602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762856,Human_RBP_ID_1520953,Human_RBP_ID_4395336,Human_RBP_ID_6528758,Human_RBP_ID_8437224 Human_Splice_Rec_1732584,Human_Splice_Rec_1732585,Human_Splice_Rec_1732590,Human_Splice_Rec_1732591,Human_Splice_Rec_1732596,Human_Splice_Rec_1732597,Human_Splice_Rec_1732604,Human_Splice_Rec_1732605,Human_Splice_Rec_1732610,Human_Splice_Rec_1732611,Human_Splice_Rec_1732616 93009 RMVar_ID_93009 Human_SNP_ID_607122781 m1A Human chr16 - 69132688 69132688 69132688 AGCCGCTTCCCACGCCCCTTCCCCAACTCACCAGCGGCCCCACGCTCCCCTTCCCGGTGCTCGCC AGCCGCTTCCCACGCCCCTTCCCCAACTCACCGGCGGCCCCACGCTCCCCTTCCCGGTGCTCGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:69132617..69133600;chr16:69131306..69133600 26863196 MeRIP-seq:(Medium) rs1481366566 Functional Loss SNV dbSNP153 33..33 33 - - - 93010 RMVar_ID_93010 Human_SNP_ID_607125926 m1A Human chr16 - 69143286 69143286 69143286 AGTCCCAGAACTGCACCTTCCCAGCAGAGTCCACACTTATGATAGTGCCATCGGACAAGAAGGCG AGTCCCAGAACTGCACCTTCCCAGCAGAGTCCGCACTTATGATAGTGCCATCGGACAAGAAGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69143237..69143308 26863196 MeRIP-seq:(Medium) rs538321215 Functional Loss SNV dbSNP153 33..33 33 - - - 93011 RMVar_ID_93011 Human_SNP_ID_607138744 m1A Human chr16 + 69187185 69187176 69187185 GCTGCCTGACTGGAATGAGGGTAGCTGCGGCGACTGCGGCGGCTGGAGCGGGGCCGGCCATGGCG GCTGCCTGACTGGAATGAGGGTAG_________CTGCGGCGGCTGGAGCGGGGCCGGCCATGGCG GCTGCGGCGA G UTP4,SNTB2 Ensembl:ENSG00000141076,Ensembl:ENSG00000168807 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr16:69187126..69187738;chr16:69187126..69187375 26863196 MeRIP-seq:(Medium) rs771173459 Functional Loss DEL dbSNP153 25..33 33 - - - 93012 RMVar_ID_93012 Human_SNP_ID_607138751 m1A Human chr16 + 69187185 69187185 69187185 GCTGCCTGACTGGAATGAGGGTAGCTGCGGCGACTGCGGCGGCTGGAGCGGGGCCGGCCATGGCG GCTGCCTGACTGGAATGAGGGTAGCTGCGGCGGCTGCGGCGGCTGGAGCGGGGCCGGCCATGGCG A G UTP4,SNTB2 Ensembl:ENSG00000141076,Ensembl:ENSG00000168807 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr16:69187126..69187738;chr16:69187126..69187375 26863196 MeRIP-seq:(Medium) rs751283655 Functional Loss SNV dbSNP153 33..33 33 - - - 93013 RMVar_ID_93013 Human_SNP_ID_607141270 m1A Human chr16 + 69197265 69197265 69197265 GAGAACTTGGAATAAGTGAGCAAGTAGTAGGAATGTATTTTGGGTCAAGTGAGAGAAGGGTGGGA GAGAACTTGGAATAAGTGAGCAAGTAGTAGGAGTGTATTTTGGGTCAAGTGAGAGAAGGGTGGGA A G UTP4,SNTB2 Ensembl:ENSG00000141076,Ensembl:ENSG00000168807 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69197259..69197401 26863196 MeRIP-seq:(Medium) rs927675314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23697115 93014 RMVar_ID_93014 Human_SNP_ID_607167903 m1A Human chr16 + 69303188 69303188 69303188 CGTGCCTGGCCCACAATAAATTTTCATTTCAGAGAAGGAAAAAAATCTCTTGAACGTCCAGAAAT CGTGCCTGGCCCACAATAAATTTTCATTTCAGGGAAGGAAAAAAATCTCTTGAACGTCCAGAAAT A G SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8053471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12786924 GWAS_ID_12121,GWAS_ID_12122,GWAS_ID_12123,GWAS_ID_12124,GWAS_ID_12125 93015 RMVar_ID_93015 Human_SNP_ID_607170774 m1A Human chr16 + 69314759 69314759 69314759 TTCTTCCTTGCAGATAAGAGAGGGCTGAACAAATGCCCCGGCCCTGCCAAGAGCCGGTCAGGAGG TTCTTCCTTGCAGATAAGAGAGGGCTGAACAAGTGCCCCGGCCCTGCCAAGAGCCGGTCAGGAGG A G VPS4A,AC026464.4 Ensembl:ENSG00000132612,Ensembl:ENSG00000260914 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69314752..69314903 26863196 MeRIP-seq:(Medium) rs1315181330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80196,RMVar_hsa_circ_95764,RMVar_hsa_circ_179380,RMVar_hsa_circ_179381 93016 RMVar_ID_93016 Human_SNP_ID_607171100 m1A Human chr16 - 69316019 69316019 69316019 GCTTTGTCCTCCTCTGTGGCTTTCGTCACCAGATCAATGGCTTTCTGGAAAGGCAAAGCAAATGG GCTTTGTCCTCCTCTGTGGCTTTCGTCACCAGGTCAATGGCTTTCTGGAAAGGCAAAGCAAATGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69311399..69316125 26863196 MeRIP-seq:(Medium) rs1476671875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521022 93017 RMVar_ID_93017 Human_SNP_ID_607171224 m1A Human chr16 + 69316339 69316339 69316339 TTATTTACGAAGCAAAGAGAAACACGGCAAGAAGCCAGTCAAAGAGAACCAGAGTGAGGGCAAGG TTATTTACGAAGCAAAGAGAAACACGGCAAGAGGCCAGTCAAAGAGAACCAGAGTGAGGGCAAGG A G VPS4A,AC026464.4 Ensembl:ENSG00000132612,Ensembl:ENSG00000260914 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:69316291..69316416 26863196 MeRIP-seq:(Medium) rs532302590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892429,Human_RBP_ID_3949440,Human_RBP_ID_9373024,Human_RBP_ID_18986754,Human_RBP_ID_26330196 Human_Splice_Rec_1732869,Human_Splice_Rec_1732887 RMVar_hsa_circ_82529,RMVar_hsa_circ_80196,RMVar_hsa_circ_95764,RMVar_hsa_circ_179380,RMVar_hsa_circ_179381,RMVar_hsa_circ_84005,RMVar_hsa_circ_375219,RMVar_hsa_circ_76611,RMVar_hsa_circ_25976,RMVar_hsa_circ_59180,RMVar_hsa_circ_179385,RMVar_hsa_circ_179386,RMVar_hsa_circ_179384,RMVar_hsa_circ_179387 93018 RMVar_ID_93018 Human_SNP_ID_607173804 m1A Human chr16 - 69323406 69323406 69323406 TCAGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCCACGCTGAGAGGATCACTTGAGCCCAGCA TCAGCTCATGCTTGTAATCCCAGCACTTTGGGGGGCCACGCTGAGAGGATCACTTGAGCCCAGCA T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9931701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27444628 GWAS_ID_12126,GWAS_ID_12127,GWAS_ID_12128 93019 RMVar_ID_93019 Human_SNP_ID_607176400 m1A Human chr16 - 69330134 69330134 69330134 CCCGCCCCGCCAGCGCGCGCTCCGCCAAATGGAGCCCTTCCCCCTGCGCGTGTTCGTGAACCCCA CCCGCCCCGCCAGCGCGCGCTCCGCCAAATGGTGCCCTTCCCCCTGCGCGTGTTCGTGAACCCCA T A PDF,AC026464.6,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000272617,Ensembl:ENSG00000213380 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:69330112..69330450 32194978 MeRIP-seq:(Medium) rs775729370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326042,Human_RBP_ID_18682727 Human_miRNA_ID_2946082 RMVar_hsa_circ_114921,RMVar_hsa_circ_179397,RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 93020 RMVar_ID_93020 Human_SNP_ID_607176401 m1A Human chr16 - 69330134 69330134 69330134 CCCGCCCCGCCAGCGCGCGCTCCGCCAAATGGAGCCCTTCCCCCTGCGCGTGTTCGTGAACCCCA CCCGCCCCGCCAGCGCGCGCTCCGCCAAATGGGGCCCTTCCCCCTGCGCGTGTTCGTGAACCCCA T C PDF,AC026464.6,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000272617,Ensembl:ENSG00000213380 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:69330112..69330450 32194978 MeRIP-seq:(Medium) rs775729370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326042,Human_RBP_ID_18682727 Human_miRNA_ID_2946082 RMVar_hsa_circ_114921,RMVar_hsa_circ_179397,RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 93021 RMVar_ID_93021 Human_SNP_ID_607176403 m1A Human chr16 - 69330139 69330139 69330139 GAGTGCCCGCCCCGCCAGCGCGCGCTCCGCCAAATGGAGCCCTTCCCCCTGCGCGTGTTCGTGAA GAGTGCCCGCCCCGCCAGCGCGCGCTCCGCCAGATGGAGCCCTTCCCCCTGCGCGTGTTCGTGAA T C PDF,AC026464.6,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000272617,Ensembl:ENSG00000213380 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1016499466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18682727 Human_miRNA_ID_2946082 RMVar_hsa_circ_114921,RMVar_hsa_circ_179397,RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 93022 RMVar_ID_93022 Human_SNP_ID_607176410 m1A Human chr16 + 69330146 69330146 69330146 ACACGCGCAGGGGGAAGGGCTCCATTTGGCGGAGCGCGCGCTGGCGGGGCGGGCACTCCCGACAC ACACGCGCAGGGGGAAGGGCTCCATTTGGCGGGGCGCGCGCTGGCGGGGCGGGCACTCCCGACAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:69330101..69330600 26863196 MeRIP-seq:(Medium) rs370832882 Functional Loss SNV dbSNP153 33..33 33 - - - 93023 RMVar_ID_93023 Human_SNP_ID_607176529 m1A Human chr16 + 69330347 69330324 69330348 GCGCCCGCTCCACCGGGGCCGCCACGCCGCGCAGCACCGGGTCCCCGACTTGGCACACGTGCGAG GCGCCCGCTC________________________CACCGGGTCCCCGACTTGGCACACGTGCGAG CCACCGGGGCCGCCACGCCGCGCAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69330101..69330600 26863196 MeRIP-seq:(Medium) rs1486421884 Functional Loss DEL dbSNP153 11..34 33 - - - 93024 RMVar_ID_93024 Human_SNP_ID_607176544 m1A Human chr16 + 69330347 69330347 69330347 GCGCCCGCTCCACCGGGGCCGCCACGCCGCGCAGCACCGGGTCCCCGACTTGGCACACGTGCGAG GCGCCCGCTCCACCGGGGCCGCCACGCCGCGCGGCACCGGGTCCCCGACTTGGCACACGTGCGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69330101..69330600 26863196 MeRIP-seq:(Medium) rs1256877856 Functional Loss SNV dbSNP153 33..33 33 - - - 93025 RMVar_ID_93025 Human_SNP_ID_607176651 m1A Human chr16 + 69330521 69330521 69330521 GGACACCGACGGCTGCCGCCCCGCCCCACGGCACGGCCGCCCACAGTGGCCAAAGACTCAGCGCG GGACACCGACGGCTGCCGCCCCGCCCCACGGCGCGGCCGCCCACAGTGGCCAAAGACTCAGCGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:69330112..69330600 26863410 MeRIP-seq:(Medium) rs1331856407 Functional Loss SNV dbSNP153 33..33 33 - - - 93026 RMVar_ID_93026 Human_SNP_ID_607176662 m1A Human chr16 - 69330535 69330535 69330535 GCCCGGCTGTGGGGCGCGCTGAGTCTTTGGCCACTGTGGGCGGCCGTGCCGTGGGGCGGGGCGGC GCCCGGCTGTGGGGCGCGCTGAGTCTTTGGCCGCTGTGGGCGGCCGTGCCGTGGGGCGGGGCGGC T C PDF,AC026464.6,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000272617,Ensembl:ENSG00000213380 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:69330449..69330550 26863410 MeRIP-seq:(Medium) rs1297751993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234337,Human_RBP_ID_818283,Human_RBP_ID_4393209,Human_RBP_ID_5358405,Human_RBP_ID_17653533,Human_RBP_ID_22441572,Human_RBP_ID_22715372,Human_RBP_ID_26757910 RMVar_hsa_circ_114921,RMVar_hsa_circ_179397,RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 93027 RMVar_ID_93027 Human_SNP_ID_607176667 m1A Human chr16 + 69330541 69330539 69330541 CCGCCCCACGGCACGGCCGCCCACAGTGGCCAAAGACTCAGCGCGCCCCACAGCCGGGCCATGGC CCGCCCCACGGCACGGCCGCCCACAGTGGCC__AGACTCAGCGCGCCCCACAGCCGGGCCATGGC CAA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:69330365..69330575 26863196 MeRIP-seq:(Medium) rs1458359625 Functional Loss DEL dbSNP153 32..33 33 - - - 93028 RMVar_ID_93028 Human_SNP_ID_607176669 m1A Human chr16 + 69330541 69330541 69330541 CCGCCCCACGGCACGGCCGCCCACAGTGGCCAAAGACTCAGCGCGCCCCACAGCCGGGCCATGGC CCGCCCCACGGCACGGCCGCCCACAGTGGCCAGAGACTCAGCGCGCCCCACAGCCGGGCCATGGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:69330365..69330575 26863196 MeRIP-seq:(Medium) rs1345312116 Functional Loss SNV dbSNP153 33..33 33 - - - 93029 RMVar_ID_93029 Human_SNP_ID_607178408 m1A Human chr16 + 69335193 69335193 69335193 ATGGACCGGAGCCAAGCATCTCGGGCCTGAAGAAACTTCACCCTCAACTCAGCCTCAGTGAAGAC ATGGACCGGAGCCAAGCATCTCGGGCCTGAAGCAACTTCACCCTCAACTCAGCCTCAGTGAAGAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69334998..69335249 32194978 MeRIP-seq:(Medium) rs142530290 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93030 RMVar_ID_93030 Human_SNP_ID_607178470 m1A Human chr16 - 69335326 69335326 69335326 GTATTGTCAGGGCATCGTGAACGAAGTGCGCCAGTCCATGCAGCTGATGCTGAGCCAGCTGATCC GTATTGTCAGGGCATCGTGAACGAAGTGCGCCGGTCCATGCAGCTGATGCTGAGCCAGCTGATCC T C AC026464.3,COG8,AC026464.1 Ensembl:ENSG00000260371,Ensembl:ENSG00000213380,Ensembl:ENSG00000259900 Protein coding,Protein coding,Protein coding CDS,CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69335275..69336636 32194978 MeRIP-seq:(Medium) rs1364070163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1732916,Human_Splice_Rec_1732917,Human_Splice_Rec_1732922,Human_Splice_Rec_1732932,Human_Splice_Rec_1732942,Human_Splice_Rec_1732948,Human_Splice_Rec_1732956,Human_Splice_Rec_1732962,Human_Splice_Rec_1732970 Human_miRNA_ID_1981135,Human_miRNA_ID_1982859 RMVar_hsa_circ_9610,RMVar_hsa_circ_98220,RMVar_hsa_circ_179396,RMVar_hsa_circ_179400,RMVar_hsa_circ_80003 93031 RMVar_ID_93031 Human_SNP_ID_607179746 m1A Human chr16 - 69339513 69339508 69339514 CCGCGGCGACTATCCCATCGGTAGCCACGGCCACAGCAGCGGCTCTCGGCGAGGTGGAGGATGAA CCGCGGCGACTATCCCATCGGTAGCCACGGC______AGCGGCTCTCGGCGAGGTGGAGGATGAA TGCTGTG T AC026464.3,COG8,AC026464.1 Ensembl:ENSG00000260371,Ensembl:ENSG00000213380,Ensembl:ENSG00000259900 Protein coding,Protein coding,Protein coding intron,CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69339425..69339526 26863196 MeRIP-seq:(Medium) rs760106237 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_234339,Human_RBP_ID_18418765,Human_RBP_ID_22442130 RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 93032 RMVar_ID_93032 Human_SNP_ID_607179955 m1A Human chr16 - 69339839 69339839 69339839 CTCAAACATGACACGGGTCTCCTCTTCAGTCAAAGGCCGCATTTTTCCCCCTGGGTTGGAACACC CTCAAACATGACACGGGTCTCCTCTTCAGTCAGAGGCCGCATTTTTCCCCCTGGGTTGGAACACC T C AC026464.3,AC026464.1 Ensembl:ENSG00000260371,Ensembl:ENSG00000259900 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69339767..69340066 26863196 MeRIP-seq:(Medium) rs769898686 Functional Loss SNV dbSNP153 33..33 33 - - - 93033 RMVar_ID_93033 Human_SNP_ID_607179959 m1A Human chr16 + 69339847 69339845 69339847 AACCCAGGGGGAAAAATGCGGCCTTTGACTGAAGAGGAGACCCGTGTCATGTTTGAGAAGATAGC AACCCAGGGGGAAAAATGCGGCCTTTGACTG__GAGGAGACCCGTGTCATGTTTGAGAAGATAGC GAA G NIP7 Ensembl:ENSG00000132603 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:69339717..69339903;chr16:69339695..69340003 26863196 MeRIP-seq:(Medium) rs753573745 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1521174,Human_RBP_ID_1845259,Human_RBP_ID_4379920,Human_RBP_ID_6529602,Human_RBP_ID_8437420,Human_RBP_ID_18418766,Human_RBP_ID_23697269,Human_RBP_ID_26329138 Human_Splice_Rec_1732977,Human_Splice_Rec_1732981,Human_Splice_Rec_1732989,Human_Splice_Rec_1732995 93034 RMVar_ID_93034 Human_SNP_ID_607179961 m1A Human chr16 + 69339847 69339847 69339847 AACCCAGGGGGAAAAATGCGGCCTTTGACTGAAGAGGAGACCCGTGTCATGTTTGAGAAGATAGC AACCCAGGGGGAAAAATGCGGCCTTTGACTGACGAGGAGACCCGTGTCATGTTTGAGAAGATAGC A C NIP7 Ensembl:ENSG00000132603 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:69339717..69339903;chr16:69339695..69340003 26863196 MeRIP-seq:(Medium) rs772073790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521174,Human_RBP_ID_1845259,Human_RBP_ID_4379920,Human_RBP_ID_6529602,Human_RBP_ID_8437420,Human_RBP_ID_18418766,Human_RBP_ID_23697269,Human_RBP_ID_26329138 Human_Splice_Rec_1732977,Human_Splice_Rec_1732981,Human_Splice_Rec_1732989,Human_Splice_Rec_1732995 93035 RMVar_ID_93035 Human_SNP_ID_607179962 m1A Human chr16 + 69339847 69339847 69339847 AACCCAGGGGGAAAAATGCGGCCTTTGACTGAAGAGGAGACCCGTGTCATGTTTGAGAAGATAGC AACCCAGGGGGAAAAATGCGGCCTTTGACTGAGGAGGAGACCCGTGTCATGTTTGAGAAGATAGC A G NIP7 Ensembl:ENSG00000132603 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:69339717..69339903;chr16:69339695..69340003 26863196 MeRIP-seq:(Medium) rs772073790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521174,Human_RBP_ID_1845259,Human_RBP_ID_4379920,Human_RBP_ID_6529602,Human_RBP_ID_8437420,Human_RBP_ID_18418766,Human_RBP_ID_23697269,Human_RBP_ID_26329138 Human_Splice_Rec_1732977,Human_Splice_Rec_1732981,Human_Splice_Rec_1732989,Human_Splice_Rec_1732995 93036 RMVar_ID_93036 Human_SNP_ID_607187378 m1A Human chr16 - 69366952 69366952 69366952 GTGGCTCGGAACTGCAGCCCAAGAACAAGCGCATGACAATAAGCAGATTGGTCTTGGAGGAGGAC GTGGCTCGGAACTGCAGCCCAAGAACAAGCGCGTGACAATAAGCAGATTGGTCTTGGAGGAGGAC T C TERF2 Ensembl:ENSG00000132604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69366901..69367015 26863196 MeRIP-seq:(Medium) rs1275325268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373034 RMVar_hsa_circ_33460,RMVar_hsa_circ_76940,RMVar_hsa_circ_304990,RMVar_hsa_circ_367686,RMVar_hsa_circ_352995,RMVar_hsa_circ_179403,RMVar_hsa_circ_179404,RMVar_hsa_circ_179402,RMVar_hsa_circ_266141,RMVar_hsa_circ_337272,RMVar_hsa_circ_355993,RMVar_hsa_circ_46401,RMVar_hsa_circ_179405 93037 RMVar_ID_93037 Human_SNP_ID_607187379 m1A Human chr16 - 69366952 69366952 69366952 GTGGCTCGGAACTGCAGCCCAAGAACAAGCGCATGACAATAAGCAGATTGGTCTTGGAGGAGGAC GTGGCTCGGAACTGCAGCCCAAGAACAAGCGCCTGACAATAAGCAGATTGGTCTTGGAGGAGGAC T G TERF2 Ensembl:ENSG00000132604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69366901..69367015 26863196 MeRIP-seq:(Medium) rs1275325268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373034 RMVar_hsa_circ_33460,RMVar_hsa_circ_76940,RMVar_hsa_circ_304990,RMVar_hsa_circ_367686,RMVar_hsa_circ_352995,RMVar_hsa_circ_179403,RMVar_hsa_circ_179404,RMVar_hsa_circ_179402,RMVar_hsa_circ_266141,RMVar_hsa_circ_337272,RMVar_hsa_circ_355993,RMVar_hsa_circ_46401,RMVar_hsa_circ_179405 93038 RMVar_ID_93038 Human_SNP_ID_607203341 m1A Human chr16 + 69428677 69428677 69428677 ACTCCGTCACAAATGAAAAAAAAAAGAAAAATAATACAGGGAAGAGGACTGTGGAATATTTATGT ACTCCGTCACAAATGAAAAAAAAAAGAAAAATTATACAGGGAAGAGGACTGTGGAATATTTATGT A T CYB5B Ensembl:ENSG00000103018 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69428674..69428797 26863196 MeRIP-seq:(Medium) rs149609803 Functional Loss SNV dbSNP153 33..33 33 - - - 93039 RMVar_ID_93039 Human_SNP_ID_607207474 m1A Human chr16 - 69447155 69447155 69447155 CCAGCTTGTTCCAGCAGAACCTCTTCTCCTCCAGGGTGCTACAAGGAAAAGATATTTACTGAACC CCAGCTTGTTCCAGCAGAACCTCTTCTCCTCCGGGGTGCTACAAGGAAAAGATATTTACTGAACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:69447151..69447200;chr16:69447151..69447225 26863196 MeRIP-seq:(Medium) rs751501732 Functional Loss SNV dbSNP153 33..33 33 - - - 93040 RMVar_ID_93040 Human_SNP_ID_607211327 m1A Human chr16 - 69463375 69463375 69463375 CCAGTTTTCTAAAGAAAGATTACTCTGAATTCACCAGGGTTCTATCACCCCAATTCATCCCTACC CCAGTTTTCTAAAGAAAGATTACTCTGAATTCCCCAGGGTTCTATCACCCCAATTCATCCCTACC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69463326..69463375 32194978 MeRIP-seq:(Medium) rs1483042932 Functional Loss SNV dbSNP153 33..33 33 - - - 93041 RMVar_ID_93041 Human_SNP_ID_607237107 m1A Human chr16 - 69565593 69565593 69565593 AGCCGGGGACGGACCCCAGAGGCCGGCGGCGGACGGGCCTGGCTGGCCCGGGGTCTCGCAGGGGA AGCCGGGGACGGACCCCAGAGGCCGGCGGCGGCCGGGCCTGGCTGGCCCGGGGTCTCGCAGGGGA T G L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:69565542..69565729 26863196 MeRIP-seq:(Medium) rs554956165 Functional Loss SNV dbSNP153 33..33 33 - - - 93042 RMVar_ID_93042 Human_SNP_ID_607237147 m1A Human chr16 - 69565715 69565706 69565716 GCTGGGGCCCCGGGGAGGGAAAAGGTATTTGCAACGACCTGGTGGCGGCGAGCCTGAGGCGGCCG GCTGGGGCCCCGGGGAGGGAAAAGGTATTTG__________GTGGCGGCGAGCCTGAGGCGGCCG CCAGGTCGTTG C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69565544..69565739 26863196 MeRIP-seq:(Medium) rs1328462033 Functional Loss DEL dbSNP153 32..41 33 - - - 93043 RMVar_ID_93043 Human_SNP_ID_607237357 m1A Human chr16 + 69566034 69566034 69566034 GTCAGTTTTCGCTGAGGAGAAACACGAAACGGACCCTTTGGCTCTCCCCCTTCCCCTTCCCCGTC GTCAGTTTTCGCTGAGGAGAAACACGAAACGGGCCCTTTGGCTCTCCCCCTTCCCCTTCCCCGTC A G NFAT5 Ensembl:ENSG00000102908 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:69565939..69566311 26863196 MeRIP-seq:(Medium) rs903489282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17077575,Human_RBP_ID_18940456,Human_RBP_ID_22053340,Human_RBP_ID_22941237,Human_RBP_ID_26442965 93044 RMVar_ID_93044 Human_SNP_ID_607237368 m1A Human chr16 - 69566053 69566048 69566053 GACCAGGAGAGGGGTTCAGGACGGGGAAGGGGAAGGGGGAGAGCCAAAGGGTCCGTTTCGTGTTT GACCAGGAGAGGGGTTCAGGACGGGGAAGGGG_____GGAGAGCCAAAGGGTCCGTTTCGTGTTT CCCCTT C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:69565965..69566057 26863410 MeRIP-seq:(Medium) rs199570325 Functional Loss DEL dbSNP153 33..37 33 - - - 93045 RMVar_ID_93045 Human_SNP_ID_607237418 m1A Human chr16 - 69566199 69566186 69566200 CCGGGACCGCGGGCACCGAACCGGGGGCGGCGACGCGAGGGCGGCTGCCGCTGCCTCCTCCTCGA CCGGGACCGCGGGCACCGAACCGGGGGCGGC______________TGCCGCTGCCTCCTCCTCGA AGCCGCCCTCGCGTC A L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69565993..69566350 26863196 MeRIP-seq:(Medium) rs1374031782 Functional Loss DEL dbSNP153 32..45 33 - - - 93046 RMVar_ID_93046 Human_SNP_ID_607237420 m1A Human chr16 - 69566194 69566194 69566194 ACCGCGGGCACCGAACCGGGGGCGGCGACGCGAGGGCGGCTGCCGCTGCCTCCTCCTCGAGGGTA ACCGCGGGCACCGAACCGGGGGCGGCGACGCGTGGGCGGCTGCCGCTGCCTCCTCCTCGAGGGTA T A L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:69566001..69566375 26863196 MeRIP-seq:(Medium) rs984785742 Functional Loss SNV dbSNP153 33..33 33 - - - 93047 RMVar_ID_93047 Human_SNP_ID_607245212 m1A Human chr16 - 69597136 69597136 69597136 ATACTGAATTTCTTTCAATTCTTCAATACACCAAGCTCTCATTTACCTCCAAAACTTCTAACATG ATACTGAATTTCTTTCAATTCTTCAATACACCGAGCTCTCATTTACCTCCAAAACTTCTAACATG T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69597111..69597258 26863196 MeRIP-seq:(Medium) rs763433860 Functional Loss SNV dbSNP153 33..33 33 - - - 93048 RMVar_ID_93048 Human_SNP_ID_607246029 m1A Human chr16 + 69600343 69600343 69600343 ATTTGAATGGGGAGTGGTTGGAACAGAAGCCAAGTAGTAGTTGGTTGAGTAATAAATGTGAATAG ATTTGAATGGGGAGTGGTTGGAACAGAAGCCAGGTAGTAGTTGGTTGAGTAATAAATGTGAATAG A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69600333..69600563 26863196 MeRIP-seq:(Medium) rs1315563286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 93049 RMVar_ID_93049 Human_SNP_ID_607246049 m1A Human chr16 + 69600448 69600448 69600448 TAAGGATGGTTGTGAGGGGAAGGAGAGAGTGGAAACTAGAAAGGCATATATAAGAATAGGAATCT TAAGGATGGTTGTGAGGGGAAGGAGAGAGTGGGAACTAGAAAGGCATATATAAGAATAGGAATCT A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69600439..69600535 26863196 MeRIP-seq:(Medium) rs764040442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817569 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 93050 RMVar_ID_93050 Human_SNP_ID_607249812 m1A Human chr16 - 69616255 69616255 69616255 GTGTTCACTGGGCAAGAGAGGGGGAGCCCAGCACGGGGAGTTACAATCCAAGCAGGGTGAGGAGG GTGTTCACTGGGCAAGAGAGGGGGAGCCCAGCGCGGGGAGTTACAATCCAAGCAGGGTGAGGAGG T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:69616175..69616315 26863196 MeRIP-seq:(Medium) rs1210249522 Functional Loss SNV dbSNP153 33..33 33 - - - 93051 RMVar_ID_93051 Human_SNP_ID_607272310 m1A Human chr16 + 69710904 69710904 69710904 GGAAAAAGAAAAACACAAATCTTAAAAACTAAAGCAAGTCAGGGAAGCCTGGAAAGATACCCAGA GGAAAAAGAAAAACACAAATCTTAAAAACTAACGCAAGTCAGGGAAGCCTGGAAAGATACCCAGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69710864..69710963 32194978 MeRIP-seq:(Medium) rs577562308 Functional Loss SNV dbSNP153 33..33 33 - - - 93052 RMVar_ID_93052 Human_SNP_ID_607281822 m1A Human chr16 - 69744459 69744459 69744459 AGAATCGGGAGGGAAGGATTGGAGGACGAATGAGTGGCACTGGCTTCTCCCAGCAGTAAAATAGC AGAATCGGGAGGGAAGGATTGGAGGACGAATGGGTGGCACTGGCTTCTCCCAGCAGTAAAATAGC T C NOB1 Ensembl:ENSG00000141101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69744457..69744605 26863196 MeRIP-seq:(Medium) rs757418627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107685,RMVar_hsa_circ_114942,RMVar_hsa_circ_117319,RMVar_hsa_circ_112970,RMVar_hsa_circ_179442,RMVar_hsa_circ_179444,RMVar_hsa_circ_179445,RMVar_hsa_circ_179443 93053 RMVar_ID_93053 Human_SNP_ID_607281823 m1A Human chr16 - 69744459 69744459 69744459 AGAATCGGGAGGGAAGGATTGGAGGACGAATGAGTGGCACTGGCTTCTCCCAGCAGTAAAATAGC AGAATCGGGAGGGAAGGATTGGAGGACGAATGCGTGGCACTGGCTTCTCCCAGCAGTAAAATAGC T G NOB1 Ensembl:ENSG00000141101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69744457..69744605 26863196 MeRIP-seq:(Medium) rs757418627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107685,RMVar_hsa_circ_114942,RMVar_hsa_circ_117319,RMVar_hsa_circ_112970,RMVar_hsa_circ_179442,RMVar_hsa_circ_179444,RMVar_hsa_circ_179445,RMVar_hsa_circ_179443 93054 RMVar_ID_93054 Human_SNP_ID_607282023 m1A Human chr16 + 69744925 69744925 69744925 GCACCTTGGGGTTGCGGGAGAAGTGCATGTGCAGGGTGCCGTCGTCGCTGACGGTCACGGACACT GCACCTTGGGGTTGCGGGAGAAGTGCATGTGCGGGGTGCCGTCGTCGCTGACGGTCACGGACACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69744823..69744979 26863196 MeRIP-seq:(Medium) rs745439543 Functional Loss SNV dbSNP153 33..33 33 - - - 93055 RMVar_ID_93055 Human_SNP_ID_607283291 m1A Human chr16 - 69748985 69748985 69748985 AACCCCCAGTAACATCAAGCAGATCCAGCAGGAGCTGGAGCAGTGTGACGTCCCCGAGGACGTGC AACCCCCAGTAACATCAAGCAGATCCAGCAGGGGCTGGAGCAGTGTGACGTCCCCGAGGACGTGC T C NOB1 Ensembl:ENSG00000141101 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69748976..69749025 26863196 MeRIP-seq:(Medium) rs1292954268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947862,Human_RBP_ID_9373067,Human_RBP_ID_18984120,Human_RBP_ID_26328201,Human_RBP_ID_27811934 Human_Splice_Rec_1733481,Human_Splice_Rec_1733495,Human_Splice_Rec_1733509 Human_miRNA_ID_2512789,Human_miRNA_ID_3055612 RMVar_hsa_circ_107685,RMVar_hsa_circ_117319,RMVar_hsa_circ_112970,RMVar_hsa_circ_65703,RMVar_hsa_circ_179442,RMVar_hsa_circ_179444,RMVar_hsa_circ_179443,RMVar_hsa_circ_353810,RMVar_hsa_circ_34455 93056 RMVar_ID_93056 Human_SNP_ID_607284924 m1A Human chr16 + 69754680 69754680 69754680 CAGCGAGCCGCCTGCGTGTGGCCTTGTCCCGAATCTCAGTGACCACCTCCCGGATGGTGTAAATG CAGCGAGCCGCCTGCGTGTGGCCTTGTCCCGAGTCTCAGTGACCACCTCCCGGATGGTGTAAATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69754557..69754925 26863196 MeRIP-seq:(Medium) rs1382529224 Functional Loss SNV dbSNP153 33..33 33 - - - 93057 RMVar_ID_93057 Human_SNP_ID_607284934 m1A Human chr16 - 69754702 69754702 69754702 GTCCGCAGGACATCGGGAAGAACATTTACACCATCCGGGAGGTGGTCACTGAGATTCGGGACAAG GTCCGCAGGACATCGGGAAGAACATTTACACCGTCCGGGAGGTGGTCACTGAGATTCGGGACAAG T C NOB1 Ensembl:ENSG00000141101 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:69754653..69754874 26863196 MeRIP-seq:(Medium) rs768064932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44983,Human_RBP_ID_478601,Human_RBP_ID_890673,Human_RBP_ID_1845514,Human_RBP_ID_12792546,Human_RBP_ID_17880110,Human_RBP_ID_18190540,Human_RBP_ID_18682946,Human_RBP_ID_22053354 Human_Splice_Rec_1733472,Human_Splice_Rec_1733488,Human_Splice_Rec_1733502 Human_miRNA_ID_1957489,Human_miRNA_ID_2016761 RMVar_hsa_circ_112970,RMVar_hsa_circ_179442 93058 RMVar_ID_93058 Human_SNP_ID_607284950 m1A Human chr16 + 69754750 69754750 69754750 CCCGATGTCCTGCGGACAGAACGCCCCAGCTCAGACCCACCCGCACCAAGCAACGCTCCGCGCGA CCCGATGTCCTGCGGACAGAACGCCCCAGCTCCGACCCACCCGCACCAAGCAACGCTCCGCGCGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:69754725..69754858 26863196 MeRIP-seq:(Medium) rs201300304 Functional Loss SNV dbSNP153 33..33 33 - - - 93059 RMVar_ID_93059 Human_SNP_ID_607319156 m1A Human chr16 + 69888137 69888137 69888137 CTGCTGCACCCTTGAGTGTGACCCCGAATCCCAACACGACTTCTCTCCCTGCCCCAGCCACACCG CTGCTGCACCCTTGAGTGTGACCCCGAATCCCTACACGACTTCTCTCCCTGCCCCAGCCACACCG A T WWP2 Ensembl:ENSG00000198373 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69888087..69888189 26863196 MeRIP-seq:(Medium) rs977924804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27560378 Human_Splice_Rec_1733540,Human_Splice_Rec_1733632,Human_Splice_Rec_1733644,Human_Splice_Rec_1733690,Human_Splice_Rec_1733698,Human_Splice_Rec_1733732 Human_miRNA_ID_233231,Human_miRNA_ID_1365059,Human_miRNA_ID_2137310,Human_miRNA_ID_2609946,Human_miRNA_ID_2666097 RMVar_hsa_circ_3147,RMVar_hsa_circ_14205,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_318947,RMVar_hsa_circ_122846,RMVar_hsa_circ_179459,RMVar_hsa_circ_309684,RMVar_hsa_circ_84734,RMVar_hsa_circ_268531,RMVar_hsa_circ_179460,RMVar_hsa_circ_179461,RMVar_hsa_circ_360520,RMVar_hsa_circ_373654,RMVar_hsa_circ_179463,RMVar_hsa_circ_41540,RMVar_hsa_circ_179462 93060 RMVar_ID_93060 Human_SNP_ID_607332870 m1A Human chr16 - 69940091 69940091 69940091 GGGTCGGGGGAACTGCAGGGCCTCCTGGGATCAGGCTTTTCTGCCAGCAGCGAGATGACAGTGTG GGGTCGGGGGAACTGCAGGGCCTCCTGGGATCGGGCTTTTCTGCCAGCAGCGAGATGACAGTGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69940043..69940132 26863196 MeRIP-seq:(Medium) rs1040551690 Functional Loss SNV dbSNP153 33..33 33 - - - 93061 RMVar_ID_93061 Human_SNP_ID_607332871 m1A Human chr16 - 69940091 69940091 69940091 GGGTCGGGGGAACTGCAGGGCCTCCTGGGATCAGGCTTTTCTGCCAGCAGCGAGATGACAGTGTG GGGTCGGGGGAACTGCAGGGCCTCCTGGGATCCGGCTTTTCTGCCAGCAGCGAGATGACAGTGTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:69940043..69940132 26863196 MeRIP-seq:(Medium) rs1040551690 Functional Loss SNV dbSNP153 33..33 33 - - - 93062 RMVar_ID_93062 Human_SNP_ID_607359240 m1A Human chr16 - 70039082 70039082 70039082 TCTTTCTCTTATAGTTGCTTAAGAAAAAAAAAAACTTGAAGCAACGCCAGTTGAATGAGGGAAGT TCTTTCTCTTATAGTTGCTTAAGAAAAAAAAATACTTGAAGCAACGCCAGTTGAATGAGGGAAGT T A PDXDC2P,AC009022.1 Ensembl:ENSG00000255185,Ensembl:ENSG00000196696 Pseudogene,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70038986..70039128 26863196 MeRIP-seq:(Medium) rs1319472922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1734054 RMVar_hsa_circ_266162,RMVar_hsa_circ_15271,RMVar_hsa_circ_91912,RMVar_hsa_circ_179480,RMVar_hsa_circ_70010,RMVar_hsa_circ_376091,RMVar_hsa_circ_179491,RMVar_hsa_circ_351129,RMVar_hsa_circ_351652 93063 RMVar_ID_93063 Human_SNP_ID_607380665 m1A Human chr16 + 70118141 70118141 70118141 TTGCTGAGGAAAAGCAGCAAAAAGGGAGGGAAACGTTGCAGGTACATGAAAGAGAGATAGCAGTT TTGCTGAGGAAAAGCAGCAAAAAGGGAGGGAAGCGTTGCAGGTACATGAAAGAGAGATAGCAGTT A G PDPR Ensembl:ENSG00000090857 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:70118101..70118209 26863196 MeRIP-seq:(Medium) rs1198117634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815816 RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 93064 RMVar_ID_93064 Human_SNP_ID_607395897 m1A Human chr16 + 70158560 70158558 70158560 ACCACTCCTAGTGATTACTGACTTTAGTGCCTAAACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA ACCACTCCTAGTGATTACTGACTTTAGTGCC__AACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA CTA C PDPR Ensembl:ENSG00000090857 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs147147897 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18287002 Human_miRNA_ID_736151 RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 93065 RMVar_ID_93065 Human_SNP_ID_607395900 m1A Human chr16 + 70158560 70158558 70158561 ACCACTCCTAGTGATTACTGACTTTAGTGCCTAAACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA ACCACTCCTAGTGATTACTGACTTTAGTGCC___ACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA CTAA C PDPR Ensembl:ENSG00000090857 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1567569975 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18287002 Human_miRNA_ID_736151 RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 93066 RMVar_ID_93066 Human_SNP_ID_607395901 m1A Human chr16 + 70158560 70158559 70158561 ACCACTCCTAGTGATTACTGACTTTAGTGCCTAAACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA ACCACTCCTAGTGATTACTGACTTTAGTGCCT__ACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA TAA T PDPR Ensembl:ENSG00000090857 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs71385645 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18287002 Human_miRNA_ID_736151 RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 93067 RMVar_ID_93067 Human_SNP_ID_607421184 m1A Human chr16 + 70251030 70251030 70251030 ACTGGAGGCCGATGGCGCGGGTCTTTTCGTGGACGGCGGCAGCACGGTCCTCGGCTTGCGTCCGT ACTGGAGGCCGATGGCGCGGGTCTTTTCGTGGTCGGCGGCAGCACGGTCCTCGGCTTGCGTCCGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70250980..70251150 26863196 MeRIP-seq:(Medium) rs1225215660 Functional Loss SNV dbSNP153 33..33 33 - - - 93068 RMVar_ID_93068 Human_SNP_ID_607421208 m1A Human chr16 + 70251063 70251063 70251063 CGGCGGCAGCACGGTCCTCGGCTTGCGTCCGTAGTTGCTCAGGCTTCTGGTTCAGGGCTGGGCGG CGGCGGCAGCACGGTCCTCGGCTTGCGTCCGTGGTTGCTCAGGCTTCTGGTTCAGGGCTGGGCGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70251012..70251150 26863196 MeRIP-seq:(Medium) rs1323038061 Functional Loss SNV dbSNP153 33..33 33 - - - 93069 RMVar_ID_93069 Human_SNP_ID_607421242 m1A Human chr16 - 70251105 70251105 70251105 TGCAGCAGAGCCTGGTGCGGGCCGCCCGCCGCAGGGGCGCCGCCGCCCAGCCCTGAACCAGAAGC TGCAGCAGAGCCTGGTGCGGGCCGCCCGCCGCCGGGGCGCCGCCGCCCAGCCCTGAACCAGAAGC T G EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70251055..70251180 26863196 MeRIP-seq:(Medium) rs899462834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763078,Human_RBP_ID_8437794,Human_RBP_ID_22051375,Human_RBP_ID_26948116,Human_RBP_ID_27245066 93070 RMVar_ID_93070 Human_SNP_ID_607421266 m1A Human chr16 - 70251134 70251134 70251134 CGAGGGCTGCCAGCGCCTCTACCCCGTGCTGCAGCAGAGCCTGGTGCGGGCCGCCCGCCGCAGGG CGAGGGCTGCCAGCGCCTCTACCCCGTGCTGCGGCAGAGCCTGGTGCGGGCCGCCCGCCGCAGGG T C EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:70251033..70251583 26863410 MeRIP-seq:(Medium) rs1208267329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22441578 93071 RMVar_ID_93071 Human_SNP_ID_607421742 m1A Human chr16 - 70251848 70251845 70251848 CATCCGCGGCCCTGAAGAATCGCAGCCGCCGCAGCTGTACGCGGCCGACGAGGAGGAGGCGCCCG CATCCGCGGCCCTGAAGAATCGCAGCCGCCGC___TGTACGCGGCCGACGAGGAGGAGGCGCCCG AGCT A EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70251351..70251975 26863196 MeRIP-seq:(Medium) rs1353803684 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_235265,Human_RBP_ID_4380677,Human_RBP_ID_6531722,Human_RBP_ID_22054200,Human_RBP_ID_22714399 93072 RMVar_ID_93072 Human_SNP_ID_607421744 m1A Human chr16 - 70251848 70251848 70251848 CATCCGCGGCCCTGAAGAATCGCAGCCGCCGCAGCTGTACGCGGCCGACGAGGAGGAGGCGCCCG CATCCGCGGCCCTGAAGAATCGCAGCCGCCGCTGCTGTACGCGGCCGACGAGGAGGAGGCGCCCG T A EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70251351..70251975 26863196 MeRIP-seq:(Medium) rs1199047319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235265,Human_RBP_ID_4380677,Human_RBP_ID_6531722,Human_RBP_ID_22054200,Human_RBP_ID_22714399 93073 RMVar_ID_93073 Human_SNP_ID_607421786 m1A Human chr16 - 70251887 70251887 70251887 TCGCACGCCAAGAACCGCCATGCCTGGGGATCACCGCCGCATCCGCGGCCCTGAAGAATCGCAGC TCGCACGCCAAGAACCGCCATGCCTGGGGATCTCCGCCGCATCCGCGGCCCTGAAGAATCGCAGC T A EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70251582..70251950 26863196 MeRIP-seq:(Medium) rs529346561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521473,Human_RBP_ID_4380677,Human_RBP_ID_5496032,Human_RBP_ID_6531724,Human_RBP_ID_12794620,Human_RBP_ID_18438017,Human_RBP_ID_18683096,Human_RBP_ID_22053365,Human_RBP_ID_22204666,Human_RBP_ID_22714399,Human_RBP_ID_27444874 Human_miRNA_ID_1194222 93074 RMVar_ID_93074 Human_SNP_ID_607421787 m1A Human chr16 - 70251887 70251887 70251887 TCGCACGCCAAGAACCGCCATGCCTGGGGATCACCGCCGCATCCGCGGCCCTGAAGAATCGCAGC TCGCACGCCAAGAACCGCCATGCCTGGGGATCGCCGCCGCATCCGCGGCCCTGAAGAATCGCAGC T C EXOSC6 Ensembl:ENSG00000223496 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70251582..70251950 26863196 MeRIP-seq:(Medium) rs529346561 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1521473,Human_RBP_ID_4380677,Human_RBP_ID_5496032,Human_RBP_ID_6531724,Human_RBP_ID_12794620,Human_RBP_ID_18438017,Human_RBP_ID_18683096,Human_RBP_ID_22053365,Human_RBP_ID_22204666,Human_RBP_ID_22714399,Human_RBP_ID_27444874 Human_miRNA_ID_1194222 93075 RMVar_ID_93075 Human_SNP_ID_607421793 m1A Human chr16 + 70251895 70251895 70251895 TCTTCAGGGCCGCGGATGCGGCGGTGATCCCCAGGCATGGCGGTTCTTGGCGTGCGAACCCCTTC TCTTCAGGGCCGCGGATGCGGCGGTGATCCCCCGGCATGGCGGTTCTTGGCGTGCGAACCCCTTC A C HSALNG0112427 RNACentral:URS0000EB9C5D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70251617..70251950 26863196 MeRIP-seq:(Medium) rs1210457327 Functional Loss SNV dbSNP153 33..33 33 - - - 93076 RMVar_ID_93076 Human_SNP_ID_607422124 m1A Human chr16 + 70252731 70252731 70252731 TGGGAGCCTCCTCCTTCCCCACTCAGTTCTTTACATCCCCGAGGCGCAGCTGGGCGAAGGAAGTG TGGGAGCCTCCTCCTTCCCCACTCAGTTCTTTGCATCCCCGAGGCGCAGCTGGGCGAAGGAAGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:70252501..70252800 32194978 MeRIP-seq:(Medium) rs1029517336 Functional Loss SNV dbSNP153 33..33 33 - - - 93077 RMVar_ID_93077 Human_SNP_ID_607422612 m1A Human chr16 + 70254027 70254027 70254027 AATTCATCCTTCTGCCACTGGGGGATGACTGCAGTGGCCAGGGCCTGGAACCAATAGACGACCAT AATTCATCCTTCTGCCACTGGGGGATGACTGCGGTGGCCAGGGCCTGGAACCAATAGACGACCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70253978..70254063 26863196 MeRIP-seq:(Medium) rs761717573 Functional Loss SNV dbSNP153 33..33 33 - - - 93078 RMVar_ID_93078 Human_SNP_ID_607423229 m1A Human chr16 - 70255693 70255693 70255693 GAGCAGGTCAGGCTGGTTTGTGGCTTATCTGAAGAAGGCAAGAGGAGCCCAGTCTGCGAATCCAT GAGCAGGTCAGGCTGGTTTGTGGCTTATCTGAGGAAGGCAAGAGGAGCCCAGTCTGCGAATCCAT T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70255690..70255814 26863196 MeRIP-seq:(Medium) rs751421844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5358424,Human_RBP_ID_19071981,Human_RBP_ID_22356390,Human_RBP_ID_22654431,Human_RBP_ID_26779279 RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_104782,RMVar_hsa_circ_110665,RMVar_hsa_circ_102846,RMVar_hsa_circ_91493,RMVar_hsa_circ_95320,RMVar_hsa_circ_99353,RMVar_hsa_circ_93392,RMVar_hsa_circ_82118,RMVar_hsa_circ_82188,RMVar_hsa_circ_179532,RMVar_hsa_circ_179540,RMVar_hsa_circ_76551,RMVar_hsa_circ_179542,RMVar_hsa_circ_179543,RMVar_hsa_circ_179541,RMVar_hsa_circ_179536,RMVar_hsa_circ_179538,RMVar_hsa_circ_179539,RMVar_hsa_circ_179537,RMVar_hsa_circ_179534,RMVar_hsa_circ_179535,RMVar_hsa_circ_179533,RMVar_hsa_circ_76998,RMVar_hsa_circ_75642,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_358152,RMVar_hsa_circ_109290,RMVar_hsa_circ_179549,RMVar_hsa_circ_123518,RMVar_hsa_circ_179550,RMVar_hsa_circ_113281,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_179552 93079 RMVar_ID_93079 Human_SNP_ID_607425297 m1A Human chr16 - 70262449 70262449 70262449 GAAGATGTTCGTGGAAGAGGTGTCCACAGGCCAGGAGTGTGGAGTGGTGCTGGACAAGACCTGTT GAAGATGTTCGTGGAAGAGGTGTCCACAGGCCGGGAGTGTGGAGTGGTGCTGGACAAGACCTGTT T C AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:70262293..70262565;chr16:70262302..70262472 26863196 MeRIP-seq:(Medium) rs1276426551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233236,Human_RBP_ID_3949473,Human_RBP_ID_6531781,Human_RBP_ID_8812435,Human_RBP_ID_9257050,Human_RBP_ID_9285863,Human_RBP_ID_12794803,Human_RBP_ID_17883550,Human_RBP_ID_22944466 Human_Splice_Rec_1734758,Human_Splice_Rec_1734796,Human_Splice_Rec_1734812 Human_miRNA_ID_2301279,Human_miRNA_ID_2301280,Human_miRNA_ID_2304543,Human_miRNA_ID_2304544,Human_miRNA_ID_2307808,Human_miRNA_ID_2307809,Human_miRNA_ID_2708976,Human_miRNA_ID_2708977 RMVar_hsa_circ_2025,RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_91493,RMVar_hsa_circ_99353,RMVar_hsa_circ_93392,RMVar_hsa_circ_82118,RMVar_hsa_circ_82188,RMVar_hsa_circ_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179536,RMVar_hsa_circ_179538,RMVar_hsa_circ_179539,RMVar_hsa_circ_179537,RMVar_hsa_circ_179534,RMVar_hsa_circ_179535,RMVar_hsa_circ_179533,RMVar_hsa_circ_76998,RMVar_hsa_circ_75642,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_109290,RMVar_hsa_circ_179549,RMVar_hsa_circ_123518,RMVar_hsa_circ_179550,RMVar_hsa_circ_113281,RMVar_hsa_circ_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555,RMVar_hsa_circ_40313,RMVar_hsa_circ_11576,RMVar_hsa_circ_179562,RMVar_hsa_circ_49717,RMVar_hsa_circ_332434,RMVar_hsa_circ_375222,RMVar_hsa_circ_324254,RMVar_hsa_circ_273456,RMVar_hsa_circ_286801,RMVar_hsa_circ_101642,RMVar_hsa_circ_179564,RMVar_hsa_circ_179565,RMVar_hsa_circ_179563,RMVar_hsa_circ_100575,RMVar_hsa_circ_179560,RMVar_hsa_circ_179561,RMVar_hsa_circ_269986,RMVar_hsa_circ_277436,RMVar_hsa_circ_319248,RMVar_hsa_circ_122626,RMVar_hsa_circ_77343,RMVar_hsa_circ_50084,RMVar_hsa_circ_31010,RMVar_hsa_circ_179570,RMVar_hsa_circ_179572,RMVar_hsa_circ_179573,RMVar_hsa_circ_179571,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569,RMVar_hsa_circ_105986,RMVar_hsa_circ_374593,RMVar_hsa_circ_179575,RMVar_hsa_circ_179576 93080 RMVar_ID_93080 Human_SNP_ID_607425300 m1A Human chr16 - 70262454 70262454 70262454 AGGGAGAAGATGTTCGTGGAAGAGGTGTCCACAGGCCAGGAGTGTGGAGTGGTGCTGGACAAGAC AGGGAGAAGATGTTCGTGGAAGAGGTGTCCACGGGCCAGGAGTGTGGAGTGGTGCTGGACAAGAC T C AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70262404..70262575 26863196 MeRIP-seq:(Medium) rs1273011840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233236,Human_RBP_ID_3949473,Human_RBP_ID_6531781,Human_RBP_ID_8812435,Human_RBP_ID_9257050,Human_RBP_ID_9285863,Human_RBP_ID_12794803,Human_RBP_ID_17883550,Human_RBP_ID_22944466 Human_Splice_Rec_1734758,Human_Splice_Rec_1734796,Human_Splice_Rec_1734812 Human_miRNA_ID_2708976,Human_miRNA_ID_2708977 RMVar_hsa_circ_2025,RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_91493,RMVar_hsa_circ_99353,RMVar_hsa_circ_93392,RMVar_hsa_circ_82118,RMVar_hsa_circ_82188,RMVar_hsa_circ_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179536,RMVar_hsa_circ_179538,RMVar_hsa_circ_179539,RMVar_hsa_circ_179537,RMVar_hsa_circ_179534,RMVar_hsa_circ_179535,RMVar_hsa_circ_179533,RMVar_hsa_circ_76998,RMVar_hsa_circ_75642,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_109290,RMVar_hsa_circ_179549,RMVar_hsa_circ_123518,RMVar_hsa_circ_179550,RMVar_hsa_circ_113281,RMVar_hsa_circ_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555,RMVar_hsa_circ_40313,RMVar_hsa_circ_11576,RMVar_hsa_circ_179562,RMVar_hsa_circ_49717,RMVar_hsa_circ_332434,RMVar_hsa_circ_375222,RMVar_hsa_circ_324254,RMVar_hsa_circ_273456,RMVar_hsa_circ_286801,RMVar_hsa_circ_101642,RMVar_hsa_circ_179564,RMVar_hsa_circ_179565,RMVar_hsa_circ_179563,RMVar_hsa_circ_100575,RMVar_hsa_circ_179560,RMVar_hsa_circ_179561,RMVar_hsa_circ_269986,RMVar_hsa_circ_277436,RMVar_hsa_circ_319248,RMVar_hsa_circ_122626,RMVar_hsa_circ_77343,RMVar_hsa_circ_50084,RMVar_hsa_circ_31010,RMVar_hsa_circ_179570,RMVar_hsa_circ_179572,RMVar_hsa_circ_179573,RMVar_hsa_circ_179571,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569,RMVar_hsa_circ_105986,RMVar_hsa_circ_374593,RMVar_hsa_circ_179575,RMVar_hsa_circ_179576 93081 RMVar_ID_93081 Human_SNP_ID_607426392 m1A Human chr16 - 70265590 70265590 70265590 AGTGGATCTGACTGGACTGATTGCTGAAGAGAAGGGCCTGGTGGTAGACATGGATGGCTTTGAAG AGTGGATCTGACTGGACTGATTGCTGAAGAGAGGGGCCTGGTGGTAGACATGGATGGCTTTGAAG T C AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70265493..70265709 26863196 MeRIP-seq:(Medium) rs758372672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277827,Human_RBP_ID_1521578,Human_RBP_ID_1845632,Human_RBP_ID_3498429,Human_RBP_ID_3947887,Human_RBP_ID_5571970,Human_RBP_ID_6531796,Human_RBP_ID_8437833,Human_RBP_ID_8809570,Human_RBP_ID_9373096,Human_RBP_ID_12794875,Human_RBP_ID_18683154,Human_RBP_ID_22441074,Human_RBP_ID_22498315,Human_RBP_ID_22944468,Human_RBP_ID_26329165 Human_Splice_Rec_1734754,Human_Splice_Rec_1734755,Human_Splice_Rec_1734806,Human_Splice_Rec_1734807 Human_miRNA_ID_3118565,Human_miRNA_ID_3118566 RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_93392,RMVar_hsa_circ_82118,RMVar_hsa_circ_82188,RMVar_hsa_circ_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179536,RMVar_hsa_circ_179537,RMVar_hsa_circ_179534,RMVar_hsa_circ_179535,RMVar_hsa_circ_179533,RMVar_hsa_circ_76998,RMVar_hsa_circ_75642,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_109290,RMVar_hsa_circ_179549,RMVar_hsa_circ_123518,RMVar_hsa_circ_179550,RMVar_hsa_circ_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_40313,RMVar_hsa_circ_11576,RMVar_hsa_circ_179562,RMVar_hsa_circ_332434,RMVar_hsa_circ_375222,RMVar_hsa_circ_324254,RMVar_hsa_circ_286801,RMVar_hsa_circ_101642,RMVar_hsa_circ_179564,RMVar_hsa_circ_179563,RMVar_hsa_circ_100575,RMVar_hsa_circ_179560,RMVar_hsa_circ_179561,RMVar_hsa_circ_277436,RMVar_hsa_circ_319248,RMVar_hsa_circ_122626,RMVar_hsa_circ_77343,RMVar_hsa_circ_50084,RMVar_hsa_circ_179577,RMVar_hsa_circ_31010,RMVar_hsa_circ_179570,RMVar_hsa_circ_179572,RMVar_hsa_circ_179571,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569,RMVar_hsa_circ_374593,RMVar_hsa_circ_292131,RMVar_hsa_circ_179576,RMVar_hsa_circ_376243,RMVar_hsa_circ_376996,RMVar_hsa_circ_319138,RMVar_hsa_circ_12494,RMVar_hsa_circ_119896,RMVar_hsa_circ_179579,RMVar_hsa_circ_179580,RMVar_hsa_circ_179578,RMVar_hsa_circ_32788,RMVar_hsa_circ_264996 93082 RMVar_ID_93082 Human_SNP_ID_607426416 m1A Human chr16 + 70265655 70265655 70265655 GGAAACCCATAGGTGTCATAGAGGAGCCAAGCAGTGTCTCCTACACAGCACAAAGGAGGTGTGTC GGAAACCCATAGGTGTCATAGAGGAGCCAAGCGGTGTCTCCTACACAGCACAAAGGAGGTGTGTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:70265526..70265675 32194978 MeRIP-seq:(Medium) rs748544878 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_526 93083 RMVar_ID_93083 Human_SNP_ID_607427960 m1A Human chr16 - 70270252 70270252 70270252 GCCTGGAACGACTGGTATCTGTGCTGCAGAATAAGATGTCCAACTATGACACTGACCTTTTTGTC GCCTGGAACGACTGGTATCTGTGCTGCAGAATCAGATGTCCAACTATGACACTGACCTTTTTGTC T G AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70270160..70270293 26863196 MeRIP-seq:(Medium) rs770790585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521601,Human_RBP_ID_1845639,Human_RBP_ID_4380840,Human_RBP_ID_5576753,Human_RBP_ID_6531821,Human_RBP_ID_12794987,Human_RBP_ID_18683173,Human_RBP_ID_22941451,Human_RBP_ID_23698008 Human_Splice_Rec_1734746,Human_Splice_Rec_1734747 RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_82118,RMVar_hsa_circ_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179534,RMVar_hsa_circ_179533,RMVar_hsa_circ_76998,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_46263,RMVar_hsa_circ_179554,RMVar_hsa_circ_11576,RMVar_hsa_circ_324254,RMVar_hsa_circ_101642,RMVar_hsa_circ_100575,RMVar_hsa_circ_179560,RMVar_hsa_circ_179561,RMVar_hsa_circ_122626,RMVar_hsa_circ_77343,RMVar_hsa_circ_50084,RMVar_hsa_circ_179570,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569,RMVar_hsa_circ_376996,RMVar_hsa_circ_12494,RMVar_hsa_circ_119896,RMVar_hsa_circ_179580,RMVar_hsa_circ_589,RMVar_hsa_circ_96218,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_7020,RMVar_hsa_circ_179583,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584 93084 RMVar_ID_93084 Human_SNP_ID_607428548 m1A Human chr16 + 70271897 70271897 70271897 CCAATCCGGTCGTAGTGGATCTCACTGCAAGGACCACAGGGGCCCGTGTCACCCATCTCCCAGAA CCAATCCGGTCGTAGTGGATCTCACTGCAAGGGCCACAGGGGCCCGTGTCACCCATCTCCCAGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70271846..70271917 26863196 MeRIP-seq:(Medium) rs1238452818 Functional Loss SNV dbSNP153 33..33 33 - - - 93085 RMVar_ID_93085 Human_SNP_ID_607430474 m1A Human chr16 - 70277057 70277057 70277057 CAATACCCAGAAGTGCATCCGGGCTGGGGGCAAACATAATGACCTGGACGATGTGGGCAAGGATG CAATACCCAGAAGTGCATCCGGGCTGGGGGCACACATAATGACCTGGACGATGTGGGCAAGGATG T G AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70277013..70277193 26863196 MeRIP-seq:(Medium) rs786205157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005297,Human_RBP_ID_6531853,Human_RBP_ID_12795221,Human_RBP_ID_17256156,Human_RBP_ID_17371530,Human_RBP_ID_17880208 Human_Splice_Rec_1734740,Human_Splice_Rec_1734741 Clinvar_Rec_527 RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_82118,RMVar_hsa_circ_179532,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_101642,RMVar_hsa_circ_179560,RMVar_hsa_circ_122626,RMVar_hsa_circ_179568,RMVar_hsa_circ_12494,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_7020,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584,RMVar_hsa_circ_47503,RMVar_hsa_circ_281927,RMVar_hsa_circ_331613,RMVar_hsa_circ_47298 93086 RMVar_ID_93086 Human_SNP_ID_607434486 m1A Human chr16 + 70289328 70289328 70289328 AGACTGGGCTTCTCCAGGCCACGCGGGGCCTGATCCTGGGGCCCACTGCGGCTGCGGAGCTTTCC AGACTGGGCTTCTCCAGGCCACGCGGGGCCTGTTCCTGGGGCCCACTGCGGCTGCGGAGCTTTCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70289325..70289425 32194978 MeRIP-seq:(Medium) rs749989661 Functional Loss SNV dbSNP153 33..33 33 - - - 93087 RMVar_ID_93087 Human_SNP_ID_607437299 m1A Human chr16 + 70299260 70299248 70299260 CCGGAGCCCACGATCCCTCGTGCCATCCCTCGAATCCACCAGCACGAGCGTCCCACCCGCGCCTG CCGGAGCCCACGATCCCTCGT____________ATCCACCAGCACGAGCGTCCCACCCGCGCCTG TGCCATCCCTCGA T DDX19B,AC012184.2 Ensembl:ENSG00000157349,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70299210..70299294 26863196 MeRIP-seq:(Medium) rs1243627112 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_762718 Human_Splice_Rec_1734925,Human_Splice_Rec_1734941,Human_Splice_Rec_1734959,Human_Splice_Rec_1734967,Human_Splice_Rec_1734975,Human_Splice_Rec_1734997,Human_Splice_Rec_1735007,Human_Splice_Rec_1735027,Human_Splice_Rec_1735039,Human_Splice_Rec_1735047,Human_Splice_Rec_1735055,Human_Splice_Rec_1735069 93088 RMVar_ID_93088 Human_SNP_ID_607441646 m1A Human chr16 + 70316061 70316061 70316061 CAAACCAAGTGGAAGTCCTGCAGCGGGATCCAAACTCCCCTCTGTACTCGGTGAAGTCTTTTGAA CAAACCAAGTGGAAGTCCTGCAGCGGGATCCATACTCCCCTCTGTACTCGGTGAAGTCTTTTGAA A T AC012184.3 Ensembl:ENSG00000261777 lincRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs757659949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1735096,Human_Splice_Rec_1735104 93089 RMVar_ID_93089 Human_SNP_ID_607450175 m1A Human chr16 + 70346952 70346952 70346952 GCGAGGTTAGGGCCCGCGTTGCGACGTGGTGCAGCGCATATTTTCACAAGTGGGTCTCCCTTGTC GCGAGGTTAGGGCCCGCGTTGCGACGTGGTGCGGCGCATATTTTCACAAGTGGGTCTCCCTTGTC A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70346901..70347050 26863196 MeRIP-seq:(Medium) rs748657054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234106,Human_RBP_ID_761935,Human_RBP_ID_895506,Human_RBP_ID_4393964,Human_RBP_ID_9326051 Human_Splice_Rec_1735109,Human_Splice_Rec_1735119,Human_Splice_Rec_1735123,Human_Splice_Rec_1735143,Human_Splice_Rec_1735151,Human_Splice_Rec_1735161,Human_Splice_Rec_1735183,Human_Splice_Rec_1735193,Human_Splice_Rec_1735203,Human_Splice_Rec_1735223 RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 93090 RMVar_ID_93090 Human_SNP_ID_607450204 m1A Human chr16 + 70346998 70346998 70346998 CAAGTGGGTCTCCCTTGTCCGGGACTATGGCCACCGACTCGTGGGCCCTGGCGGTGGACGAGCAG CAAGTGGGTCTCCCTTGTCCGGGACTATGGCCGCCGACTCGTGGGCCCTGGCGGTGGACGAGCAG A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70346949..70347107 26863196 MeRIP-seq:(Medium) rs773132234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234107,Human_RBP_ID_895506,Human_RBP_ID_4393213,Human_RBP_ID_9325187,Human_RBP_ID_19074988,Human_RBP_ID_22945123,Human_RBP_ID_26329170 Human_Splice_Rec_1735109,Human_Splice_Rec_1735119,Human_Splice_Rec_1735123,Human_Splice_Rec_1735143,Human_Splice_Rec_1735151,Human_Splice_Rec_1735161,Human_Splice_Rec_1735183,Human_Splice_Rec_1735193,Human_Splice_Rec_1735203,Human_Splice_Rec_1735223 Human_miRNA_ID_2393622,Human_miRNA_ID_2574398 RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 93091 RMVar_ID_93091 Human_SNP_ID_607452868 m1A Human chr16 + 70356204 70356204 70356204 CAAACCAAGTGGAAGTCCTGCAACGGGATCCAAACTCCCCTCTGTACTCGGTGAAGTCGTTTGAA CAAACCAAGTGGAAGTCCTGCAACGGGATCCACACTCCCCTCTGTACTCGGTGAAGTCGTTTGAA A C AC012184.4 Ensembl:ENSG00000285710 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs769302675 Functional Loss SNV dbSNP153 33..33 33 - - - 93092 RMVar_ID_93092 Human_SNP_ID_607457680 m1A Human chr16 + 70372372 70372372 70372372 GTGCAGGTTGTGCGGAAGAGGCTGAGTGGAAAATGGTGTGAGCCCCACCGCTGTGCATCGAATGA GTGCAGGTTGTGCGGAAGAGGCTGAGTGGAAAGTGGTGTGAGCCCCACCGCTGTGCATCGAATGA A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:70372326..70372425 26863196 MeRIP-seq:(Medium) rs908343992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8185950,Human_RBP_ID_22053375,Human_RBP_ID_26445315,Human_RBP_ID_27811230 RMVar_hsa_circ_179599,RMVar_hsa_circ_179602 93093 RMVar_ID_93093 Human_SNP_ID_607460710 m1A Human chr16 + 70380906 70380906 70380906 TTTTTTCCAGAGCAACAGGTAGGCTGGTGAGGAGGCCTCCGGCCCAGGGAGAGGCGCTGAGAAGG TTTTTTCCAGAGCAACAGGTAGGCTGGTGAGGCGGCCTCCGGCCCAGGGAGAGGCGCTGAGAAGG A C AC012184.1 Ensembl:ENSG00000260111 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70380866..70381074 26863196 MeRIP-seq:(Medium) rs950676386 Functional Loss SNV dbSNP153 33..33 33 - - - 93094 RMVar_ID_93094 Human_SNP_ID_607460724 m1A Human chr16 + 70380923 70380923 70380923 GGTAGGCTGGTGAGGAGGCCTCCGGCCCAGGGAGAGGCGCTGAGAAGGCTGCGGGTGAACGGGAG GGTAGGCTGGTGAGGAGGCCTCCGGCCCAGGGTGAGGCGCTGAGAAGGCTGCGGGTGAACGGGAG A T AC012184.1 Ensembl:ENSG00000260111 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70380874..70380978 26863196 MeRIP-seq:(Medium) rs889996598 Functional Loss SNV dbSNP153 33..33 33 - - - 93095 RMVar_ID_93095 Human_SNP_ID_607466080 m1A Human chr16 + 70398277 70398277 70398277 CGGGGGAAATGTTACCGTCAAAGTGGCTGTCAAACCAGTCGGAGGCACCGGCATCGCCCATGCAG CGGGGGAAATGTTACCGTCAAAGTGGCTGTCAGACCAGTCGGAGGCACCGGCATCGCCCATGCAG A G AC012184.1 Ensembl:ENSG00000260111 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70398207..70398408 26863196 MeRIP-seq:(Medium) rs137977873 Functional Loss SNV dbSNP153 33..33 33 - - - 93096 RMVar_ID_93096 Human_SNP_ID_607466924 m1A Human chr16 + 70401012 70401012 70401012 GTAGATGGGAAGCCAGGTCCTTGTCTCCTCTCATTCTCCCTTTGCCTGCTGCATGCCCAACATCT GTAGATGGGAAGCCAGGTCCTTGTCTCCTCTCTTTCTCCCTTTGCCTGCTGCATGCCCAACATCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70400962..70401063 32194978 MeRIP-seq:(Medium) rs1417331011 Functional Loss SNV dbSNP153 33..33 33 - - - 93097 RMVar_ID_93097 Human_SNP_ID_607478447 m1A Human chr16 - 70439022 70438992 70439023 GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG GGACGACGGCGGCGGCGGCGGCGGCGGCGGC_______________________________CGG GGCCGCCGCCGCCGCCCGCGCAGAAAGCCGTC G ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70423061..70439224;chr16:70438841..70439217;chr16:70423061..70439231;chr16:70423061..70439190 26863196 MeRIP-seq:(Medium) rs1189829900 Functional Loss DEL dbSNP153 32..62 33 - - - Human_RBP_ID_4381120,Human_RBP_ID_5316703,Human_RBP_ID_5419564,Human_RBP_ID_5524574,Human_RBP_ID_9325192,Human_RBP_ID_17121684,Human_RBP_ID_22532826,Human_RBP_ID_23118626 Human_Splice_Rec_1735295,Human_Splice_Rec_1735325,Human_Splice_Rec_1735329 93098 RMVar_ID_93098 Human_SNP_ID_607478451 m1A Human chr16 - 70439022 70438994 70439022 GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG GGACGACGGCGGCGGCGGCGGCGGCGGCGGCG____________________________GCCGG CCGCCGCCGCCGCCCGCGCAGAAAGCCGT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70423061..70439224;chr16:70438841..70439217;chr16:70423061..70439231;chr16:70423061..70439190 26863196 MeRIP-seq:(Medium) rs1290656060 Functional Loss DEL dbSNP153 33..60 33 - - - Human_RBP_ID_4381120,Human_RBP_ID_5316703,Human_RBP_ID_5419564,Human_RBP_ID_5524574,Human_RBP_ID_9325192,Human_RBP_ID_17121684,Human_RBP_ID_22532826,Human_RBP_ID_23118626 Human_Splice_Rec_1735295,Human_Splice_Rec_1735325,Human_Splice_Rec_1735329 93099 RMVar_ID_93099 Human_SNP_ID_607478452 m1A Human chr16 - 70439022 70438997 70439022 GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG GGACGACGGCGGCGGCGGCGGCGGCGGCGGCG_________________________GCGGCCGG CCGCCGCCGCCCGCGCAGAAAGCCGT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70423061..70439224;chr16:70438841..70439217;chr16:70423061..70439231;chr16:70423061..70439190 26863196 MeRIP-seq:(Medium) rs1025410730 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_4381120,Human_RBP_ID_5316703,Human_RBP_ID_5419564,Human_RBP_ID_5524574,Human_RBP_ID_9325192,Human_RBP_ID_17121684,Human_RBP_ID_22532826,Human_RBP_ID_23118626 Human_Splice_Rec_1735295,Human_Splice_Rec_1735325,Human_Splice_Rec_1735329 93100 RMVar_ID_93100 Human_SNP_ID_607478460 m1A Human chr16 - 70439022 70439006 70439022 GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG GGACGACGGCGGCGGCGGCGGCGGCGGCGGCG________________GCGGCGGCGGCGGCCGG CCCGCGCAGAAAGCCGT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70423061..70439224;chr16:70438841..70439217;chr16:70423061..70439231;chr16:70423061..70439190 26863196 MeRIP-seq:(Medium) rs1350919440 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_4381120,Human_RBP_ID_5316703,Human_RBP_ID_5419564,Human_RBP_ID_5524574,Human_RBP_ID_9325192,Human_RBP_ID_17121684,Human_RBP_ID_22532826,Human_RBP_ID_23118626 Human_Splice_Rec_1735295,Human_Splice_Rec_1735325,Human_Splice_Rec_1735329 93101 RMVar_ID_93101 Human_SNP_ID_607478470 m1A Human chr16 - 70439022 70439022 70439022 GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG GGACGACGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTTTCTGCGCGGGCGGCGGCGGCGGCCGG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70423061..70439224;chr16:70438841..70439217;chr16:70423061..70439231;chr16:70423061..70439190 26863196 MeRIP-seq:(Medium) rs1174621621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4381120,Human_RBP_ID_5316703,Human_RBP_ID_5419564,Human_RBP_ID_5524574,Human_RBP_ID_9325192,Human_RBP_ID_17121684,Human_RBP_ID_22532826,Human_RBP_ID_23118626 Human_Splice_Rec_1735295,Human_Splice_Rec_1735325,Human_Splice_Rec_1735329 93102 RMVar_ID_93102 Human_SNP_ID_607478485 m1A Human chr16 - 70439049 70439034 70439049 ACGAGAGAGCTGCGAGCTAACGGGTCCGGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCT ACGAGAGAGCTGCGAGCTAACGGGTCCGGACG_______________GCGGCGGCGGCGACGGCT CCGCCGCCGCCGCCGT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70438889..70439117 26863196 MeRIP-seq:(Medium) rs997047152 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_4381121,Human_RBP_ID_9419325,Human_RBP_ID_17124041,Human_RBP_ID_22441088,Human_RBP_ID_22532826,Human_RBP_ID_23118626 93103 RMVar_ID_93103 Human_SNP_ID_607478498 m1A Human chr16 - 70439049 70439049 70439049 ACGAGAGAGCTGCGAGCTAACGGGTCCGGACGACGGCGGCGGCGGCGGCGGCGGCGGCGACGGCT ACGAGAGAGCTGCGAGCTAACGGGTCCGGACGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70438889..70439117 26863196 MeRIP-seq:(Medium) rs1162722171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4381121,Human_RBP_ID_9419325,Human_RBP_ID_17124041,Human_RBP_ID_22441088,Human_RBP_ID_22532826,Human_RBP_ID_23118626 93104 RMVar_ID_93104 Human_SNP_ID_607478518 m1A Human chr16 - 70439092 70439092 70439092 AGGGTTGGGCCAGGCAAGGGCGGGACTAGCCCACGGCGGGCGGACGAGAGAGCTGCGAGCTAACG AGGGTTGGGCCAGGCAAGGGCGGGACTAGCCCCCGGCGGGCGGACGAGAGAGCTGCGAGCTAACG T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:70438943..70439203 26863196 MeRIP-seq:(Medium) rs987920642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393225,Human_RBP_ID_9325193,Human_RBP_ID_9419325,Human_RBP_ID_23118626 93105 RMVar_ID_93105 Human_SNP_ID_607489493 m1A Human chr16 + 70474243 70474243 70474243 CCGTGGGGGCTTGCGGAGCGGGCCAGCTGCCAACCCTGAGTGGATGCGGCCCTTCTCATACCTGG CCGTGGGGGCTTGCGGAGCGGGCCAGCTGCCAGCCCTGAGTGGATGCGGCCCTTCTCATACCTGG A G FCSK Ensembl:ENSG00000157353 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:70474192..70474333 26863196 MeRIP-seq:(Medium) rs770074270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1735387,Human_Splice_Rec_1735433,Human_Splice_Rec_1735479,Human_Splice_Rec_1735521 RMVar_hsa_circ_3974,RMVar_hsa_circ_90261,RMVar_hsa_circ_179612,RMVar_hsa_circ_87222,RMVar_hsa_circ_105099,RMVar_hsa_circ_111662,RMVar_hsa_circ_179615,RMVar_hsa_circ_179616,RMVar_hsa_circ_179617,RMVar_hsa_circ_339387,RMVar_hsa_circ_115892,RMVar_hsa_circ_179621,RMVar_hsa_circ_122500,RMVar_hsa_circ_113028,RMVar_hsa_circ_179623,RMVar_hsa_circ_179624 93106 RMVar_ID_93106 Human_SNP_ID_607491609 m1A Human chr16 + 70480734 70480734 70480734 TTGAGGGCAAGAGACTGACCATCCATGCAGAAAGCTGGCCTGGGCTGCTCGCTGCCTGCCGTGGC TTGAGGGCAAGAGACTGACCATCCATGCAGAATGCTGGCCTGGGCTGCTCGCTGCCTGCCGTGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70480685..70480832 26863196 MeRIP-seq:(Medium) rs1210860216 Functional Loss SNV dbSNP153 33..33 33 - - - 93107 RMVar_ID_93107 Human_SNP_ID_607492389 m1A Human chr16 + 70482843 70482842 70482844 GTCAGCCCTTCCTGCACAAGGACAAGGTGGAGACATGTGACACAGAAGGCACGACTCATCCCTTC GTCAGCCCTTCCTGCACAAGGACAAGGTGGAG__ATGTGACACAGAAGGCACGACTCATCCCTTC GAC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70482837..70482969 26863196 MeRIP-seq:(Medium) rs758986477 Functional Loss DEL dbSNP153 33..34 33 - - - 93108 RMVar_ID_93108 Human_SNP_ID_607492406 m1A Human chr16 + 70482868 70482868 70482868 GGTGGAGACATGTGACACAGAAGGCACGACTCATCCCTTCCCTCTCTCTTCTCCCCATCCCTTCC GGTGGAGACATGTGACACAGAAGGCACGACTCCTCCCTTCCCTCTCTCTTCTCCCCATCCCTTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70482820..70482966 26863196 MeRIP-seq:(Medium) rs1243513085 Functional Loss SNV dbSNP153 33..33 33 - - - 93109 RMVar_ID_93109 Human_SNP_ID_607500190 m1A Human chr16 - 70509185 70509185 70509185 GCTACAGGTAGGGTTTGGTAGCAGCTTTAGCGAGGAACACTGAGTAGAATAAATTGTAGGGTTTG GCTACAGGTAGGGTTTGGTAGCAGCTTTAGCGGGGAACACTGAGTAGAATAAATTGTAGGGTTTG T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70509137..70509217 26863196 MeRIP-seq:(Medium) rs781656921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892488,Human_RBP_ID_2481438,Human_RBP_ID_5355987,Human_RBP_ID_12797198,Human_RBP_ID_19072010,Human_RBP_ID_22356147 RMVar_hsa_circ_50,RMVar_hsa_circ_81662,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633,RMVar_hsa_circ_294105,RMVar_hsa_circ_367065,RMVar_hsa_circ_35411,RMVar_hsa_circ_53487,RMVar_hsa_circ_329426,RMVar_hsa_circ_347038,RMVar_hsa_circ_348334,RMVar_hsa_circ_55087 93110 RMVar_ID_93110 Human_SNP_ID_607501715 m1A Human chr16 + 70514435 70514435 70514435 GCAGCCTGCTCATAATCTTCACTCCTCAAAGCAGTCTGAACTCCATCCATGCAGAACTTCAGGTC GCAGCCTGCTCATAATCTTCACTCCTCAAAGCTGTCTGAACTCCATCCATGCAGAACTTCAGGTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70514326..70514525 26863196 MeRIP-seq:(Medium) rs1170462603 Functional Loss SNV dbSNP153 33..33 33 - - - 93111 RMVar_ID_93111 Human_SNP_ID_607502675 m1A Human chr16 - 70517720 70517720 70517720 GTATTTCTCCAGTCCTAATCTGCAGCTGATTGAGGGAGATGCAAAGCAGCTGGCTGGAATGATCA GTATTTCTCCAGTCCTAATCTGCAGCTGATTGCGGGAGATGCAAAGCAGCTGGCTGGAATGATCA T G COG4 Ensembl:ENSG00000103051 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:70517631..70517731 32194978 MeRIP-seq:(Medium) rs1268494338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521711,Human_RBP_ID_5524575,Human_RBP_ID_18984184,Human_RBP_ID_22584501 Human_Splice_Rec_1735582,Human_Splice_Rec_1735583,Human_Splice_Rec_1735618,Human_Splice_Rec_1735619,Human_Splice_Rec_1735652,Human_Splice_Rec_1735653,Human_Splice_Rec_1735688,Human_Splice_Rec_1735689,Human_Splice_Rec_1735722,Human_Splice_Rec_1735723,Human_Splice_Rec_1735756,Human_Splice_Rec_1735757,Human_Splice_Rec_1735828,Human_Splice_Rec_1735829,Human_Splice_Rec_1735838,Human_Splice_Rec_1735839,Human_Splice_Rec_1735846,Human_Splice_Rec_1735847,Human_Splice_Rec_1735860,Human_Splice_Rec_1735861 RMVar_hsa_circ_50,RMVar_hsa_circ_122105,RMVar_hsa_circ_112041,RMVar_hsa_circ_179627,RMVar_hsa_circ_179632,RMVar_hsa_circ_367065,RMVar_hsa_circ_347038,RMVar_hsa_circ_348334,RMVar_hsa_circ_23429,RMVar_hsa_circ_179635,RMVar_hsa_circ_373235,RMVar_hsa_circ_345854,RMVar_hsa_circ_179636,RMVar_hsa_circ_270314,RMVar_hsa_circ_65388,RMVar_hsa_circ_314586,RMVar_hsa_circ_179637,RMVar_hsa_circ_179638,RMVar_hsa_circ_327616 93112 RMVar_ID_93112 Human_SNP_ID_607504493 m1A Human chr16 + 70523447 70523447 70523447 CAGCTCTGTCAGGGAGCGAATGAGCTCAGCGGAGATTTCGGAGCAGCGGCCACCTCCCACCCCCT CAGCTCTGTCAGGGAGCGAATGAGCTCAGCGGCGATTTCGGAGCAGCGGCCACCTCCCACCCCCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:70523380..70523527 26863196 MeRIP-seq:(Medium) rs761374483 Functional Loss SNV dbSNP153 33..33 33 - - - 93113 RMVar_ID_93113 Human_SNP_ID_607504524 m1A Human chr16 + 70523494 70523494 70523494 GGCCACCTCCCACCCCCTCAGACGGCTGCTGCACCCCTGACAGCTTCGGAGGCGAATCAAGGTCC GGCCACCTCCCACCCCCTCAGACGGCTGCTGCGCCCCTGACAGCTTCGGAGGCGAATCAAGGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70523351..70523550;chr16:70523376..70523550;chr16:70523401..70523550 26863196 MeRIP-seq:(Medium) rs780394487 Functional Loss SNV dbSNP153 33..33 33 - - - 93114 RMVar_ID_93114 Human_SNP_ID_607504525 m1A Human chr16 + 70523494 70523494 70523494 GGCCACCTCCCACCCCCTCAGACGGCTGCTGCACCCCTGACAGCTTCGGAGGCGAATCAAGGTCC GGCCACCTCCCACCCCCTCAGACGGCTGCTGCTCCCCTGACAGCTTCGGAGGCGAATCAAGGTCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70523351..70523550;chr16:70523376..70523550;chr16:70523401..70523550 26863196 MeRIP-seq:(Medium) rs780394487 Functional Loss SNV dbSNP153 33..33 33 - - - 93115 RMVar_ID_93115 Human_SNP_ID_607515107 m1A Human chr16 + 70560418 70560418 70560418 TGTGAAGTACCCAAGGGAGAGGTTTTCCCATCATAGCTGATAAGCTTCCATCAGGCTTCACCTGC TGTGAAGTACCCAAGGGAGAGGTTTTCCCATCGTAGCTGATAAGCTTCCATCAGGCTTCACCTGC A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70560414..70560541 26863196 MeRIP-seq:(Medium) rs1449666688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22652308 RMVar_hsa_circ_35580,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179640,RMVar_hsa_circ_376283,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179653,RMVar_hsa_circ_179654,RMVar_hsa_circ_86802,RMVar_hsa_circ_179662,RMVar_hsa_circ_179663,RMVar_hsa_circ_375363,RMVar_hsa_circ_58019,RMVar_hsa_circ_119000,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_338483,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668,RMVar_hsa_circ_95163,RMVar_hsa_circ_352474,RMVar_hsa_circ_123867,RMVar_hsa_circ_89946,RMVar_hsa_circ_179679,RMVar_hsa_circ_179680,RMVar_hsa_circ_179678,RMVar_hsa_circ_124155,RMVar_hsa_circ_333063,RMVar_hsa_circ_94340,RMVar_hsa_circ_115059,RMVar_hsa_circ_24064,RMVar_hsa_circ_66049,RMVar_hsa_circ_24318,RMVar_hsa_circ_179682,RMVar_hsa_circ_179681,RMVar_hsa_circ_80109,RMVar_hsa_circ_102045,RMVar_hsa_circ_179687,RMVar_hsa_circ_179688,RMVar_hsa_circ_179686,RMVar_hsa_circ_113193,RMVar_hsa_circ_6818,RMVar_hsa_circ_268098,RMVar_hsa_circ_333306,RMVar_hsa_circ_179689,RMVar_hsa_circ_305699,RMVar_hsa_circ_81194,RMVar_hsa_circ_122547,RMVar_hsa_circ_56818,RMVar_hsa_circ_179693,RMVar_hsa_circ_76553,RMVar_hsa_circ_179690,RMVar_hsa_circ_179691,RMVar_hsa_circ_24044 93116 RMVar_ID_93116 Human_SNP_ID_607516051 m1A Human chr16 + 70564049 70564049 70564049 CACGAAAGCTCAGAGAAAGCAGCAGATGGCAGAGGTAATGAGACTAACGTTCAGGGGTTCTATTA CACGAAAGCTCAGAGAAAGCAGCAGATGGCAGTGGTAATGAGACTAACGTTCAGGGGTTCTATTA A T SF3B3 Ensembl:ENSG00000189091 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70564031..70564102 26863196 MeRIP-seq:(Medium) rs1335392503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17607970,Human_RBP_ID_19075039 Human_Splice_Rec_1735909,Human_Splice_Rec_1735969,Human_Splice_Rec_1735975 RMVar_hsa_circ_316,RMVar_hsa_circ_35580,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179640,RMVar_hsa_circ_376283,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_179655,RMVar_hsa_circ_179653,RMVar_hsa_circ_179654,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_375363,RMVar_hsa_circ_58019,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_338483,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179668,RMVar_hsa_circ_95163,RMVar_hsa_circ_352474,RMVar_hsa_circ_123867,RMVar_hsa_circ_89946,RMVar_hsa_circ_179679,RMVar_hsa_circ_179680,RMVar_hsa_circ_179678,RMVar_hsa_circ_124155,RMVar_hsa_circ_333063,RMVar_hsa_circ_94340,RMVar_hsa_circ_115059,RMVar_hsa_circ_24064,RMVar_hsa_circ_179682,RMVar_hsa_circ_179681,RMVar_hsa_circ_80109,RMVar_hsa_circ_102045,RMVar_hsa_circ_179687,RMVar_hsa_circ_179688,RMVar_hsa_circ_179686,RMVar_hsa_circ_6818,RMVar_hsa_circ_268098,RMVar_hsa_circ_81194,RMVar_hsa_circ_122547,RMVar_hsa_circ_56818,RMVar_hsa_circ_179693,RMVar_hsa_circ_76553,RMVar_hsa_circ_179690,RMVar_hsa_circ_179691,RMVar_hsa_circ_24044,RMVar_hsa_circ_306611,RMVar_hsa_circ_363307,RMVar_hsa_circ_330717,RMVar_hsa_circ_179697,RMVar_hsa_circ_119421,RMVar_hsa_circ_179695,RMVar_hsa_circ_179694,RMVar_hsa_circ_362026,RMVar_hsa_circ_288221,RMVar_hsa_circ_290501,RMVar_hsa_circ_179699,RMVar_hsa_circ_115007,RMVar_hsa_circ_179698,RMVar_hsa_circ_179696 93117 RMVar_ID_93117 Human_SNP_ID_607516474 m1A Human chr16 - 70565497 70565497 70565497 CCTACCTTGTGCAAAAACTCCAGTTTTTCCCCATTGTTCACAAGCTTGTAAGTATAGACGAAGCC CCTACCTTGTGCAAAAACTCCAGTTTTTCCCCGTTGTTCACAAGCTTGTAAGTATAGACGAAGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:70565351..70565569 32194978 MeRIP-seq:(Medium) rs1206171930 Functional Loss SNV dbSNP153 33..33 33 - - - 93118 RMVar_ID_93118 Human_SNP_ID_607516475 m1A Human chr16 + 70565503 70565503 70565503 GTCTATACTTACAAGCTTGTGAACAATGGGGAAAAACTGGAGTTTTTGCACAAGGTAGGAATCTG GTCTATACTTACAAGCTTGTGAACAATGGGGATAAACTGGAGTTTTTGCACAAGGTAGGAATCTG A T SF3B3 Ensembl:ENSG00000189091 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:70565401..70565508 26863410 MeRIP-seq:(Medium) rs748833404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478856,Human_RBP_ID_1178965,Human_RBP_ID_1521867,Human_RBP_ID_1845850,Human_RBP_ID_5356886,Human_RBP_ID_8809715,Human_RBP_ID_9373131,Human_RBP_ID_18984192,Human_RBP_ID_22442176,Human_RBP_ID_22582842,Human_RBP_ID_23698312,Human_RBP_ID_26810535 Human_Splice_Rec_1735913,Human_Splice_Rec_1735973 Human_miRNA_ID_516384,Human_miRNA_ID_520612,Human_miRNA_ID_2071176,Human_miRNA_ID_2181369,Human_miRNA_ID_2183473,Human_miRNA_ID_2804102 RMVar_hsa_circ_316,RMVar_hsa_circ_35580,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179640,RMVar_hsa_circ_376283,RMVar_hsa_circ_90869,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_179653,RMVar_hsa_circ_179654,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_375363,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179668,RMVar_hsa_circ_123867,RMVar_hsa_circ_89946,RMVar_hsa_circ_179679,RMVar_hsa_circ_179680,RMVar_hsa_circ_124155,RMVar_hsa_circ_94340,RMVar_hsa_circ_115059,RMVar_hsa_circ_24064,RMVar_hsa_circ_179682,RMVar_hsa_circ_179681,RMVar_hsa_circ_80109,RMVar_hsa_circ_102045,RMVar_hsa_circ_179687,RMVar_hsa_circ_179688,RMVar_hsa_circ_179686,RMVar_hsa_circ_6818,RMVar_hsa_circ_268098,RMVar_hsa_circ_81194,RMVar_hsa_circ_56818,RMVar_hsa_circ_179693,RMVar_hsa_circ_76553,RMVar_hsa_circ_179691,RMVar_hsa_circ_24044,RMVar_hsa_circ_363307,RMVar_hsa_circ_330717,RMVar_hsa_circ_103993,RMVar_hsa_circ_179697,RMVar_hsa_circ_119421,RMVar_hsa_circ_288221,RMVar_hsa_circ_179699,RMVar_hsa_circ_115007,RMVar_hsa_circ_179698,RMVar_hsa_circ_274147,RMVar_hsa_circ_347681,RMVar_hsa_circ_365267,RMVar_hsa_circ_179701,RMVar_hsa_circ_179702 93119 RMVar_ID_93119 Human_SNP_ID_607547002 m1A Human chr16 + 70661702 70661700 70661702 ATGGAGTAGAGTATGTACAGCCCCCGGGGCTCACAGGGGAGGGGGACGGCGGAGTCGGTGGGGGC ATGGAGTAGAGTATGTACAGCCCCCGGGGCT__CAGGGGAGGGGGACGGCGGAGTCGGTGGGGGC TCA T AC020763.4 Ensembl:ENSG00000279569 Other exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:70661601..70661800 26863410 MeRIP-seq:(Medium) rs1425328862 Functional Loss DEL dbSNP153 32..33 33 - - - 93120 RMVar_ID_93120 Human_SNP_ID_607547247 m1A Human chr16 + 70662190 70662186 70662190 AAGCCTGGGAGGCTCAGACCCAGCTCCATTCTATCAATCAATCAATCAATCATCAAGACCAAGGT AAGCCTGGGAGGCTCAGACCCAGCTCCAT____TCAATCAATCAATCAATCATCAAGACCAAGGT TTCTA T AC020763.4 Ensembl:ENSG00000279569 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70662139..70662407 26863196 MeRIP-seq:(Medium) rs920916427 Functional Loss DEL dbSNP153 30..33 33 - - - 93121 RMVar_ID_93121 Human_SNP_ID_607547254 m1A Human chr16 + 70662190 70662190 70662190 AAGCCTGGGAGGCTCAGACCCAGCTCCATTCTATCAATCAATCAATCAATCATCAAGACCAAGGT AAGCCTGGGAGGCTCAGACCCAGCTCCATTCTGTCAATCAATCAATCAATCATCAAGACCAAGGT A G AC020763.4 Ensembl:ENSG00000279569 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70662139..70662407 26863196 MeRIP-seq:(Medium) rs947045720 Functional Loss SNV dbSNP153 33..33 33 - - - 93122 RMVar_ID_93122 Human_SNP_ID_607547366 m1A Human chr16 - 70662355 70662355 70662355 GCTGCCCCCACCCCACGCACCAAGTCACGCCAAGTCTCAGCAGGTAAAAGCACGTGAGCCTAGGG GCTGCCCCCACCCCACGCACCAAGTCACGCCAGGTCTCAGCAGGTAAAAGCACGTGAGCCTAGGG T C MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70661903..70662660 32194978 MeRIP-seq:(Medium) rs1216917217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93123 RMVar_ID_93123 Human_SNP_ID_607547503 m1A Human chr16 - 70662629 70662629 70662629 CGGTGGTCCTATGGCAGGATGAGAAGGGAGGGACTTGGCTCCCCCAGAGCCCGGTGGAAGCTACT CGGTGGTCCTATGGCAGGATGAGAAGGGAGGGCCTTGGCTCCCCCAGAGCCCGGTGGAAGCTACT T G MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70662580..70662898 26863196 MeRIP-seq:(Medium) rs992101928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4381596,Human_RBP_ID_5524588,Human_RBP_ID_9353242,Human_RBP_ID_23165351,Human_RBP_ID_26445345 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93124 RMVar_ID_93124 Human_SNP_ID_607547640 m1A Human chr16 - 70662888 70662888 70662888 GAGGCCGGAGGCCCTGGGGTCACCGGCCAGCCACACAGGCACCGTTTTCAGATGTCCACTTCTCA GAGGCCGGAGGCCCTGGGGTCACCGGCCAGCCGCACAGGCACCGTTTTCAGATGTCCACTTCTCA T C MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70662837..70662987 26863196 MeRIP-seq:(Medium) rs1372944694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1283052,Human_RBP_ID_5524591,Human_RBP_ID_26445349 Human_miRNA_ID_2076427 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93125 RMVar_ID_93125 Human_SNP_ID_607547961 m1A Human chr16 - 70663511 70663511 70663511 AAGACACCTCACTTGGATTCCAGCATTTAAACAGGAAGTGACTTCTTAGCAAGCCTGGCCAGGAC AAGACACCTCACTTGGATTCCAGCATTTAAACGGGAAGTGACTTCTTAGCAAGCCTGGCCAGGAC T C MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs78335918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22055181,Human_RBP_ID_27245299 Human_miRNA_ID_649143 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93126 RMVar_ID_93126 Human_SNP_ID_607547962 m1A Human chr16 - 70663511 70663511 70663511 AAGACACCTCACTTGGATTCCAGCATTTAAACAGGAAGTGACTTCTTAGCAAGCCTGGCCAGGAC AAGACACCTCACTTGGATTCCAGCATTTAAACCGGAAGTGACTTCTTAGCAAGCCTGGCCAGGAC T G MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs78335918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22055181,Human_RBP_ID_27245299 Human_miRNA_ID_649143 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93127 RMVar_ID_93127 Human_SNP_ID_607547978 m1A Human chr16 - 70663558 70663558 70663558 CCAGGAGAGAGGACAGAGCCAGGGCAGAGGCCATGCCACTTTATGGAAAGACACCTCACTTGGAT CCAGGAGAGAGGACAGAGCCAGGGCAGAGGCCGTGCCACTTTATGGAAAGACACCTCACTTGGAT T C MTSS2 Ensembl:ENSG00000132613 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70663509..70663927 26863196 MeRIP-seq:(Medium) rs1165797681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005378,Human_RBP_ID_6533065,Human_RBP_ID_27445099 Human_miRNA_ID_2063738,Human_miRNA_ID_2493712,Human_miRNA_ID_2901399 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93128 RMVar_ID_93128 Human_SNP_ID_607548566 m1A Human chr16 - 70664372 70664372 70664372 AGGGCCCGCCCGAGTTTGACAAGTCATCCACCATCCCGCGCAACAGCAACATCGCCCAGAACTAC AGGGCCCGCCCGAGTTTGACAAGTCATCCACCCTCCCGCGCAACAGCAACATCGCCCAGAACTAC T G MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:70664351..70664400 26863196 MeRIP-seq:(Medium) rs138817967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_88252,Human_miRNA_ID_1957497,Human_miRNA_ID_2250271 RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 93129 RMVar_ID_93129 Human_SNP_ID_607548949 m1A Human chr16 - 70664946 70664946 70664946 GCCCCAGCGGGGAAGAGGCACCGCGACCCCGGATGTCCCCTGCCACCATCGCAGCCAAGGTAGGC GCCCCAGCGGGGAAGAGGCACCGCGACCCCGGCTGTCCCCTGCCACCATCGCAGCCAAGGTAGGC T G MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70664644..70665526 32194978 MeRIP-seq:(Medium) rs1157457792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18469793,Human_RBP_ID_18986858 Human_Splice_Rec_1736049,Human_Splice_Rec_1736071 RMVar_hsa_circ_115261,RMVar_hsa_circ_179710,RMVar_hsa_circ_123812,RMVar_hsa_circ_179708,RMVar_hsa_circ_369493,RMVar_hsa_circ_179711 93130 RMVar_ID_93130 Human_SNP_ID_607553003 m1A Human chr16 - 70676888 70676888 70676888 CACCCAGCAGCTCCAGCTCCCGGAAGTCCAGCATGTGCAGGTCAGTGGGGGTGGGGTTCCCAGGG CACCCAGCAGCTCCAGCTCCCGGAAGTCCAGCTTGTGCAGGTCAGTGGGGGTGGGGTTCCCAGGG T A MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70674439..70676892 32194978 MeRIP-seq:(Medium) rs1202749219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233658,Human_RBP_ID_9064684,Human_RBP_ID_19075052 Human_Splice_Rec_1736042,Human_Splice_Rec_1736043,Human_Splice_Rec_1736064,Human_Splice_Rec_1736065,Human_Splice_Rec_1736076,Human_Splice_Rec_1736077,Human_Splice_Rec_1736088 RMVar_hsa_circ_115261,RMVar_hsa_circ_22883,RMVar_hsa_circ_179708,RMVar_hsa_circ_86405,RMVar_hsa_circ_372916,RMVar_hsa_circ_84703,RMVar_hsa_circ_89895,RMVar_hsa_circ_179713,RMVar_hsa_circ_179714,RMVar_hsa_circ_179715,RMVar_hsa_circ_93759,RMVar_hsa_circ_364581,RMVar_hsa_circ_179716,RMVar_hsa_circ_17940,RMVar_hsa_circ_50057,RMVar_hsa_circ_179717 93131 RMVar_ID_93131 Human_SNP_ID_607553982 m1A Human chr16 - 70679677 70679677 70679677 TGCAGAGTACAAACGAGCCCGGCATGAGATCAAAAAGAAGTCGTCGGACACGCTGAAGCTGCAGA TGCAGAGTACAAACGAGCCCGGCATGAGATCAGAAAGAAGTCGTCGGACACGCTGAAGCTGCAGA T C MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70679576..70679895 26863196 MeRIP-seq:(Medium) rs111728238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373140,Human_RBP_ID_18287163,Human_RBP_ID_18986871,Human_RBP_ID_19072047,Human_RBP_ID_26329183 Human_Splice_Rec_1736034,Human_Splice_Rec_1736035,Human_Splice_Rec_1736060,Human_Splice_Rec_1736082,Human_Splice_Rec_1736083 RMVar_hsa_circ_93759,RMVar_hsa_circ_179716,RMVar_hsa_circ_50057,RMVar_hsa_circ_104494,RMVar_hsa_circ_85203,RMVar_hsa_circ_179718,RMVar_hsa_circ_101908,RMVar_hsa_circ_179719,RMVar_hsa_circ_179720 93132 RMVar_ID_93132 Human_SNP_ID_607554165 m1A Human chr16 - 70679999 70679978 70680000 CGCTCACACGCATGTGCATGCGCCACCGCAGCATCGAGACCAAGCTGCGGCAGTTCACCAAGTGA CGCTCACACGCATGTGCATGCGCCACCGCAG______________________TTCACCAAGTGA ACTGCCGCAGCTTGGTCTCGATG A MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70677804..70685866 32194978 MeRIP-seq:(Medium) rs1312565550 Functional Loss DEL dbSNP153 32..53 33 - - - Human_RBP_ID_18984202 Human_Splice_Rec_1736030,Human_Splice_Rec_1736031,Human_Splice_Rec_1736056,Human_Splice_Rec_1736057,Human_Splice_Rec_1736079 RMVar_hsa_circ_93759,RMVar_hsa_circ_179716,RMVar_hsa_circ_50057,RMVar_hsa_circ_104494,RMVar_hsa_circ_85203,RMVar_hsa_circ_179718,RMVar_hsa_circ_179720,RMVar_hsa_circ_38347 93133 RMVar_ID_93133 Human_SNP_ID_607555962 m1A Human chr16 + 70685823 70685823 70685823 TGCTCTGGCTGGGCCGGGCCGCGGCGGCGGCTAGGCGCACGGAGCGCGGGGAGCAGCGCAAGGGA TGCTCTGGCTGGGCCGGGCCGCGGCGGCGGCTTGGCGCACGGAGCGCGGGGAGCAGCGCAAGGGA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70685776..70685987 26863196 MeRIP-seq:(Medium) rs1157874410 Functional Loss SNV dbSNP153 33..33 33 - - - 93134 RMVar_ID_93134 Human_SNP_ID_607555964 m1A Human chr16 + 70685829 70685829 70685829 GGCTGGGCCGGGCCGCGGCGGCGGCTAGGCGCACGGAGCGCGGGGAGCAGCGCAAGGGAGGGGGC GGCTGGGCCGGGCCGCGGCGGCGGCTAGGCGCCCGGAGCGCGGGGAGCAGCGCAAGGGAGGGGGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:70685738..70685942 26863196 MeRIP-seq:(Medium) rs1303814125 Functional Loss SNV dbSNP153 33..33 33 - - - 93135 RMVar_ID_93135 Human_SNP_ID_607556002 m1A Human chr16 - 70685949 70685949 70685949 ACATGGCCCGCGCCGCCCGCCGGAGGCCCGCGACCCCGGAGCGCGGCGCGGCCGGCCGCTGAGCG ACATGGCCCGCGCCGCCCGCCGGAGGCCCGCGCCCCCGGAGCGCGGCGCGGCCGGCCGCTGAGCG T G MTSS2 Ensembl:ENSG00000132613 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:70685851..70686050 26863410 MeRIP-seq:(Medium) rs990852436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393228 RMVar_hsa_circ_102921,RMVar_hsa_circ_38347,RMVar_hsa_circ_179722 93136 RMVar_ID_93136 Human_SNP_ID_607568285 m1A Human chr16 - 70730135 70730135 70730135 CAGCCGGATTCGAGAATGAGGATTCGAGACTGAGTAGGAAGTAGATTTGTCTGGTGACTGATGTG CAGCCGGATTCGAGAATGAGGATTCGAGACTGGGTAGGAAGTAGATTTGTCTGGTGACTGATGTG T C VAC14 Ensembl:ENSG00000103043 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70730087..70730247 26863196 MeRIP-seq:(Medium) rs944184142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12800265,Human_RBP_ID_23698476,Human_RBP_ID_27660132 RMVar_hsa_circ_92763,RMVar_hsa_circ_108734,RMVar_hsa_circ_103777,RMVar_hsa_circ_179724,RMVar_hsa_circ_179726,RMVar_hsa_circ_84985,RMVar_hsa_circ_179725,RMVar_hsa_circ_99834,RMVar_hsa_circ_85805,RMVar_hsa_circ_179728,RMVar_hsa_circ_179727,RMVar_hsa_circ_119900,RMVar_hsa_circ_179731,RMVar_hsa_circ_179732 93137 RMVar_ID_93137 Human_SNP_ID_607568297 m1A Human chr16 - 70730160 70730160 70730160 AGCTTGTGAGGGGGATGGGAAGCTGCAGCCGGATTCGAGAATGAGGATTCGAGACTGAGTAGGAA AGCTTGTGAGGGGGATGGGAAGCTGCAGCCGGGTTCGAGAATGAGGATTCGAGACTGAGTAGGAA T C VAC14 Ensembl:ENSG00000103043 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:70730122..70730243 26863196 MeRIP-seq:(Medium) rs937740644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6533201,Human_RBP_ID_12800267,Human_RBP_ID_23698478 RMVar_hsa_circ_92763,RMVar_hsa_circ_108734,RMVar_hsa_circ_103777,RMVar_hsa_circ_179724,RMVar_hsa_circ_179726,RMVar_hsa_circ_84985,RMVar_hsa_circ_179725,RMVar_hsa_circ_99834,RMVar_hsa_circ_85805,RMVar_hsa_circ_179728,RMVar_hsa_circ_179727,RMVar_hsa_circ_119900,RMVar_hsa_circ_179731,RMVar_hsa_circ_179732 93138 RMVar_ID_93138 Human_SNP_ID_607581955 m1A Human chr16 - 70779054 70779054 70779054 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCAATGCAGCAGCTGAAAGCTTTTT TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGGTTCCCGGCCAATGCAGCAGCTGAAAGCTTTTT T C VAC14 Ensembl:ENSG00000103043 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1567598126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43534,Human_RBP_ID_233354,Human_RBP_ID_760827,Human_RBP_ID_1522029,Human_RBP_ID_5274712,Human_RBP_ID_8812781,Human_RBP_ID_9257239,Human_RBP_ID_9286590,Human_RBP_ID_17126208,Human_RBP_ID_20170871,Human_RBP_ID_22357090,Human_RBP_ID_22531530,Human_RBP_ID_22760641,Human_RBP_ID_22802195,Human_RBP_ID_23128543,Human_RBP_ID_23698502,Human_RBP_ID_24531756,Human_RBP_ID_24552148,Human_RBP_ID_26757395,Human_RBP_ID_26781078 RMVar_hsa_circ_179726,RMVar_hsa_circ_84985,RMVar_hsa_circ_99834,RMVar_hsa_circ_94852,RMVar_hsa_circ_85805,RMVar_hsa_circ_179727,RMVar_hsa_circ_179732,RMVar_hsa_circ_39178,RMVar_hsa_circ_179734,RMVar_hsa_circ_372554,RMVar_hsa_circ_124095,RMVar_hsa_circ_95619,RMVar_hsa_circ_9496,RMVar_hsa_circ_179735,RMVar_hsa_circ_179737,RMVar_hsa_circ_179736,RMVar_hsa_circ_104593,RMVar_hsa_circ_179741 93139 RMVar_ID_93139 Human_SNP_ID_607587971 m1A Human chr16 - 70800942 70800942 70800942 GCAGACTCCCCTGGCCCCGGCGCGGCCCCGGCAGCCGCGGGCTAAGGAGTCGCGAGGTTCCCCCA GCAGACTCCCCTGGCCCCGGCGCGGCCCCGGCGGCCGCGGGCTAAGGAGTCGCGAGGTTCCCCCA T C VAC14 Ensembl:ENSG00000103043 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70800913..70801066 26863196 MeRIP-seq:(Medium) rs765329752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393230 93140 RMVar_ID_93140 Human_SNP_ID_607587972 m1A Human chr16 - 70800942 70800942 70800942 GCAGACTCCCCTGGCCCCGGCGCGGCCCCGGCAGCCGCGGGCTAAGGAGTCGCGAGGTTCCCCCA GCAGACTCCCCTGGCCCCGGCGCGGCCCCGGCCGCCGCGGGCTAAGGAGTCGCGAGGTTCCCCCA T G VAC14 Ensembl:ENSG00000103043 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:70800913..70801066 26863196 MeRIP-seq:(Medium) rs765329752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393230 93141 RMVar_ID_93141 Human_SNP_ID_607704633 m1A Human chr16 - 71288280 71288280 71288280 CAATCTTAGGTAGGCTTCACTGAGAAAATGACATTTGAGCAAATATTGGAAGGAGGTGAAGGAGT CAATCTTAGGTAGGCTTCACTGAGAAAATGACGTTTGAGCAAATATTGGAAGGAGGTGAAGGAGT T C CMTR2 Ensembl:ENSG00000180917 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71288273..71288380 26863196 MeRIP-seq:(Medium) rs1455435212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12800904 RMVar_hsa_circ_98947,RMVar_hsa_circ_179747 93142 RMVar_ID_93142 Human_SNP_ID_607741833 m1A Human chr16 + 71426550 71426550 71426550 GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGAGCCTCAGAGAGGGCAGCTGTTTTGTTGTGCTA GTCAGTCTCATAATCTGAAGGTCCTGAGTTCGGGCCTCAGAGAGGGCAGCTGTTTTGTTGTGCTA A G tRNA-Met-CAT-2-1 RNACentral:URS00006E998F tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1229112176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1527548,Human_RBP_ID_1845959,Human_RBP_ID_3498685,Human_RBP_ID_5259468,Human_RBP_ID_5274851,Human_RBP_ID_6533409,Human_RBP_ID_8252280,Human_RBP_ID_8438196,Human_RBP_ID_9064819,Human_RBP_ID_12800995,Human_RBP_ID_18683639,Human_RBP_ID_20139406,Human_RBP_ID_22498342,Human_RBP_ID_22802203,Human_RBP_ID_22941740,Human_RBP_ID_23128558,Human_RBP_ID_23698549,Human_RBP_ID_26638461,Human_RBP_ID_26948585,Human_RBP_ID_27660151 93143 RMVar_ID_93143 Human_SNP_ID_607749162 m1A Human chr16 - 71454614 71454614 71454614 GAAGGGAATCTGGTGGGGCTGGATGAGACAGAAGCCGTGGATGATCTTTGGGGGTGGCTTGAGCT GAAGGGAATCTGGTGGGGCTGGATGAGACAGAGGCCGTGGATGATCTTTGGGGGTGGCTTGAGCT T C ZNF23,AC010547.4 Ensembl:ENSG00000167377,Ensembl:ENSG00000261611 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:71454516..71454715 26863196 MeRIP-seq:(Medium) rs1416971450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12801065 RMVar_hsa_circ_46546 93144 RMVar_ID_93144 Human_SNP_ID_607809703 m1A Human chr16 - 71688727 71688726 71688727 GTTGCTTGAGAGGGAAAGAGTGAATGAGGACAAGGCTGGGGATTGGTGGAGAGGAAGCAGCAGAT GTTGCTTGAGAGGGAAAGAGTGAATGAGGACA_GGCTGGGGATTGGTGGAGAGGAAGCAGCAGAT CT C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:71688676..71688781 26863196 MeRIP-seq:(Medium) rs1252373234 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_815847 RMVar_hsa_circ_358023,RMVar_hsa_circ_378879,RMVar_hsa_circ_69085,RMVar_hsa_circ_14005,RMVar_hsa_circ_91472,RMVar_hsa_circ_123475,RMVar_hsa_circ_179779,RMVar_hsa_circ_88313,RMVar_hsa_circ_179780,RMVar_hsa_circ_179781,RMVar_hsa_circ_290439,RMVar_hsa_circ_298899,RMVar_hsa_circ_49787,RMVar_hsa_circ_179787,RMVar_hsa_circ_179788,RMVar_hsa_circ_90415,RMVar_hsa_circ_179790,RMVar_hsa_circ_372980,RMVar_hsa_circ_179793,RMVar_hsa_circ_179794,RMVar_hsa_circ_297182,RMVar_hsa_circ_333656,RMVar_hsa_circ_267363 93145 RMVar_ID_93145 Human_SNP_ID_607819420 m1A Human chr16 - 71723320 71723320 71723320 GCTTTCTCCCCTCCCGGACACCTGAAGACATCACCCCAGCGGGAGGATGGCAGCGGCGATTGGCC GCTTTCTCCCCTCCCGGACACCTGAAGACATCGCCCCAGCGGGAGGATGGCAGCGGCGATTGGCC T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71723317..71723636 26863196 MeRIP-seq:(Medium) rs1363817110 Functional Loss SNV dbSNP153 33..33 33 - - - 93146 RMVar_ID_93146 Human_SNP_ID_607819644 m1A Human chr16 - 71723860 71723860 71723860 CGTCTCTGTGAATCCTGGGTCGCCGATGGGGGAGGTGGAGCCGGGGCCCGCGGGCCCGCTGGAGC CGTCTCTGTGAATCCTGGGTCGCCGATGGGGGGGGTGGAGCCGGGGCCCGCGGGCCCGCTGGAGC T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:71723710..71723875 26863196 MeRIP-seq:(Medium) rs1426604033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234563,Human_RBP_ID_816450,Human_RBP_ID_18418773 Human_Splice_Rec_1737377,Human_Splice_Rec_1737413 93147 RMVar_ID_93147 Human_SNP_ID_607855623 m1A Human chr16 - 71846050 71846035 71846050 CAGGATCCACTCACTCGTCCCGGAGCCGCCGCAACCGCGGCCGCCGCCATCCCCGGCCCCGGAGC CAGGATCCACTCACTCGTCCCGGAGCCGCCGC_______________CATCCCCGGCCCCGGAGC GGCGGCGGCCGCGGTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:71845999..71846095;chr16:71846003..71885261 26863196 MeRIP-seq:(Medium) rs1283018267 Functional Loss DEL dbSNP153 33..47 33 - - - 93148 RMVar_ID_93148 Human_SNP_ID_607855634 m1A Human chr16 - 71846050 71846050 71846050 CAGGATCCACTCACTCGTCCCGGAGCCGCCGCAACCGCGGCCGCCGCCATCCCCGGCCCCGGAGC CAGGATCCACTCACTCGTCCCGGAGCCGCCGCGACCGCGGCCGCCGCCATCCCCGGCCCCGGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:71845999..71846095;chr16:71846003..71885261 26863196 MeRIP-seq:(Medium) rs939165476 Functional Loss SNV dbSNP153 33..33 33 - - - 93149 RMVar_ID_93149 Human_SNP_ID_607855642 m1A Human chr16 - 71846059 71846059 71846059 AGCGCTTCCCAGGATCCACTCACTCGTCCCGGAGCCGCCGCAACCGCGGCCGCCGCCATCCCCGG AGCGCTTCCCAGGATCCACTCACTCGTCCCGGGGCCGCCGCAACCGCGGCCGCCGCCATCCCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:71846013..71848050;chr16:71846012..71848050 26863196 MeRIP-seq:(Medium) rs1439475212 Functional Loss SNV dbSNP153 33..33 33 - - - 93150 RMVar_ID_93150 Human_SNP_ID_607856583 m1A Human chr16 - 71849600 71849600 71849600 CGCCCACATCTATTAGGGAACAAATCAGAGGCAAAGAAAAGTAACCTAGGGATGAGCCAAGACAA CGCCCACATCTATTAGGGAACAAATCAGAGGCTAAGAAAAGTAACCTAGGGATGAGCCAAGACAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71849597..71849689 26863196 MeRIP-seq:(Medium) rs1456008817 Functional Loss SNV dbSNP153 33..33 33 - - - 93151 RMVar_ID_93151 Human_SNP_ID_607856794 m1A Human chr16 - 71850201 71850201 71850201 TGGCAGAAGGAGATAGGAGGGGACTCGGTAGGAAATTAGGTGGCACAGCATAGGGAAGGCTATAA TGGCAGAAGGAGATAGGAGGGGACTCGGTAGGTAATTAGGTGGCACAGCATAGGGAAGGCTATAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:71850114..71850267 26863196 MeRIP-seq:(Medium) rs1276081051 Functional Loss SNV dbSNP153 33..33 33 - - - 93152 RMVar_ID_93152 Human_SNP_ID_607856941 m1A Human chr16 + 71850612 71850612 71850612 AAGACGGGAAAGTGAAGCCCTTGACTCCCCCAACAGCAAGGGTGAAGGCCAGGGACTGGTGCCAG AAGACGGGAAAGTGAAGCCCTTGACTCCCCCAGCAGCAAGGGTGAAGGCCAGGGACTGGTGCCAG A G ATXN1L,IST1 Ensembl:ENSG00000224470,Ensembl:ENSG00000182149 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:71850562..71850660 26863196 MeRIP-seq:(Medium) rs1199023664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5182854 RMVar_hsa_circ_99871,RMVar_hsa_circ_179850 93153 RMVar_ID_93153 Human_SNP_ID_607859536 m1A Human chr16 - 71860332 71860332 71860332 TGAGGGACCGTGAAGCCAAGCGCTTGCAGCGCATGCAGGAGACAGACGAGCAGCGGGCACGCCGG TGAGGGACCGTGAAGCCAAGCGCTTGCAGCGCTTGCAGGAGACAGACGAGCAGCGGGCACGCCGG T A ZNF821 Ensembl:ENSG00000102984 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:71860180..71860430 26863196 MeRIP-seq:(Medium) rs1462721816 Functional Loss SNV dbSNP153 33..33 33 - - - 93154 RMVar_ID_93154 Human_SNP_ID_607859548 m1A Human chr16 - 71860358 71860358 71860358 CCCCGAGGAGCGGGAGGTGAGGCGCATGAGGGACCGTGAAGCCAAGCGCTTGCAGCGCATGCAGG CCCCGAGGAGCGGGAGGTGAGGCGCATGAGGGGCCGTGAAGCCAAGCGCTTGCAGCGCATGCAGG T C ZNF821 Ensembl:ENSG00000102984 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71860192..71860452 26863196 MeRIP-seq:(Medium) rs1477957240 Functional Loss SNV dbSNP153 33..33 33 - - - 93155 RMVar_ID_93155 Human_SNP_ID_607860915 m1A Human chr16 - 71865393 71865393 71865393 TGGAAAGTGTTGGTAAGTCAGAGGTGGTGTACAGTGGGAATGAGCTCAGTGTAAGGTGCTTGGGG TGGAAAGTGTTGGTAAGTCAGAGGTGGTGTACGGTGGGAATGAGCTCAGTGTAAGGTGCTTGGGG T C ZNF821 Ensembl:ENSG00000102984 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71865381..71865469 26863196 MeRIP-seq:(Medium) rs1324000142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22405 93156 RMVar_ID_93156 Human_SNP_ID_607869453 m1A Human chr16 - 71895565 71895565 71895565 ACACTCACCTAACCGAATCCTGCCGTGAACGCAGCAGACACCGACTTCAGGGTTCACCATCCAAA ACACTCACCTAACCGAATCCTGCCGTGAACGCGGCAGACACCGACTTCAGGGTTCACCATCCAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:71895501..71895698 26863196 MeRIP-seq:(Medium) rs1168458874 Functional Loss SNV dbSNP153 33..33 33 - - - 93157 RMVar_ID_93157 Human_SNP_ID_607869471 m1A Human chr16 - 71895591 71895591 71895591 CAGAGACCTCTGACGCCGAGGATGCCACACTCACCTAACCGAATCCTGCCGTGAACGCAGCAGAC CAGAGACCTCTGACGCCGAGGATGCCACACTCGCCTAACCGAATCCTGCCGTGAACGCAGCAGAC T C piR-51338 RNACentral:URS00001953D4 piRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:71895551..71895653 26863410 MeRIP-seq:(Medium) rs1295976691 Functional Loss SNV dbSNP153 33..33 33 - - - 93158 RMVar_ID_93158 Human_SNP_ID_607869549 m1A Human chr16 + 71895765 71895755 71895765 AAGTGGGGGTCAGACCGGAGGTCAGGCCCTCGAGGGCCCGCGGCGCAGGAGGCTGCCCAGGCCTG AAGTGGGGGTCAGACCGGAGGTC__________GGGCCCGCGGCGCAGGAGGCTGCCCAGGCCTG CAGGCCCTCGA C IST1 Ensembl:ENSG00000182149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71895762..71895870 26863196 MeRIP-seq:(Medium) rs1020847348 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5087962,Human_RBP_ID_9326066 RMVar_hsa_circ_122289,RMVar_hsa_circ_92307,RMVar_hsa_circ_103632,RMVar_hsa_circ_179851,RMVar_hsa_circ_179852,RMVar_hsa_circ_179854,RMVar_hsa_circ_97663,RMVar_hsa_circ_179853 93159 RMVar_ID_93159 Human_SNP_ID_607876131 m1A Human chr16 + 71915709 71915709 71915709 GTGAATTTGAGATTAGTCATAAATCGCCTTAAACTATTGGAGAAAAAGAAAAGTGAGTAGTGTAC GTGAATTTGAGATTAGTCATAAATCGCCTTAAGCTATTGGAGAAAAAGAAAAGTGAGTAGTGTAC A G IST1 Ensembl:ENSG00000182149 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:71915620..71916600 26863196 MeRIP-seq:(Medium) rs1411563971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1846126,Human_RBP_ID_8083944,Human_RBP_ID_23698928 Human_Splice_Rec_1737806,Human_Splice_Rec_1737807,Human_Splice_Rec_1737812,Human_Splice_Rec_1737813,Human_Splice_Rec_1737820,Human_Splice_Rec_1737821,Human_Splice_Rec_1737840,Human_Splice_Rec_1737841,Human_Splice_Rec_1737864,Human_Splice_Rec_1737865,Human_Splice_Rec_1737868,Human_Splice_Rec_1737869,Human_Splice_Rec_1737897,Human_Splice_Rec_1737908,Human_Splice_Rec_1737909,Human_Splice_Rec_1737916,Human_Splice_Rec_1737917,Human_Splice_Rec_1737934,Human_Splice_Rec_1737935,Human_Splice_Rec_1737952,Human_Splice_Rec_1737953,Human_Splice_Rec_1737984,Human_Splice_Rec_1737985,Human_Splice_Rec_1737996,Human_Splice_Rec_1737997,Human_Splice_Rec_1738008,Human_Splice_Rec_1738009,Human_Splice_Rec_1738024,Human_Splice_Rec_1738025,Human_Splice_Rec_1738033,Human_Splice_Rec_1738041 Human_miRNA_ID_2790061,Human_miRNA_ID_2819679 RMVar_hsa_circ_37106,RMVar_hsa_circ_122289,RMVar_hsa_circ_92307,RMVar_hsa_circ_103632,RMVar_hsa_circ_179851,RMVar_hsa_circ_179852,RMVar_hsa_circ_179854,RMVar_hsa_circ_97663,RMVar_hsa_circ_313849,RMVar_hsa_circ_362283,RMVar_hsa_circ_179853,RMVar_hsa_circ_341169,RMVar_hsa_circ_306294,RMVar_hsa_circ_179856,RMVar_hsa_circ_179857,RMVar_hsa_circ_179855 93160 RMVar_ID_93160 Human_SNP_ID_607876342 m1A Human chr16 + 71916395 71916395 71916395 AGTAGAAACACCCAGTTCTTCCTGTTGGGGGGAGATTGGCCTGTAGGCCAGATGCAAGTGCTCTA AGTAGAAACACCCAGTTCTTCCTGTTGGGGGGCGATTGGCCTGTAGGCCAGATGCAAGTGCTCTA A C IST1 Ensembl:ENSG00000182149 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:71916392..71916594 26863410 MeRIP-seq:(Medium) rs1269489192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12803922 RMVar_hsa_circ_37106,RMVar_hsa_circ_122289,RMVar_hsa_circ_92307,RMVar_hsa_circ_103632,RMVar_hsa_circ_179851,RMVar_hsa_circ_179852,RMVar_hsa_circ_179854,RMVar_hsa_circ_97663,RMVar_hsa_circ_313849,RMVar_hsa_circ_362283,RMVar_hsa_circ_179853,RMVar_hsa_circ_341169,RMVar_hsa_circ_306294,RMVar_hsa_circ_179856,RMVar_hsa_circ_179857,RMVar_hsa_circ_179855 93161 RMVar_ID_93161 Human_SNP_ID_607909273 m1A Human chr16 + 72008783 72008783 72008783 ATGACGGAAGGAGCATGGCGTGGAGACACCTGAAAGTGAGTCCCGCGAGTGAGCAGTGTGGATGG ATGACGGAAGGAGCATGGCGTGGAGACACCTGCAAGTGAGTCCCGCGAGTGAGCAGTGTGGATGG A C DHODH Ensembl:ENSG00000102967 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72008774..72008910 26863196 MeRIP-seq:(Medium) rs3213422 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19075108 Human_Splice_Rec_1738347,Human_Splice_Rec_1738361,Human_Splice_Rec_1738375,Human_Splice_Rec_1738383 Clinvar_Rec_528 GWAS_ID_12129,GWAS_ID_12130,GWAS_ID_12131,GWAS_ID_12132,GWAS_ID_12133,GWAS_ID_12134,GWAS_ID_12135,GWAS_ID_12136,GWAS_ID_12137,GWAS_ID_12138,GWAS_ID_12139,GWAS_ID_12140,GWAS_ID_12141,GWAS_ID_12142,GWAS_ID_12143,GWAS_ID_12144,GWAS_ID_12145,GWAS_ID_12146,GWAS_ID_12147,GWAS_ID_12148,GWAS_ID_12149,GWAS_ID_12150,GWAS_ID_12151,GWAS_ID_12152,GWAS_ID_12153,GWAS_ID_12154,GWAS_ID_12155,GWAS_ID_12156,GWAS_ID_12157,GWAS_ID_12158,GWAS_ID_12159,GWAS_ID_12160,GWAS_ID_12161,GWAS_ID_12162,GWAS_ID_12163,GWAS_ID_12164,GWAS_ID_12165,GWAS_ID_12166,GWAS_ID_12167 93162 RMVar_ID_93162 Human_SNP_ID_607909274 m1A Human chr16 + 72008784 72008784 72008784 TGACGGAAGGAGCATGGCGTGGAGACACCTGAAAGTGAGTCCCGCGAGTGAGCAGTGTGGATGGG TGACGGAAGGAGCATGGCGTGGAGACACCTGAGAGTGAGTCCCGCGAGTGAGCAGTGTGGATGGG A G DHODH Ensembl:ENSG00000102967 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:72008778..72008996;chr16:72008782..72008924 26863196 MeRIP-seq:(Medium) rs1326426210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19075108 Human_Splice_Rec_1738347,Human_Splice_Rec_1738361,Human_Splice_Rec_1738375,Human_Splice_Rec_1738383 93163 RMVar_ID_93163 Human_SNP_ID_607911027 m1A Human chr16 + 72014669 72014669 72014669 CTTCCGCCTCCCTGAGGACCAAGCTGTCATTAACAGGTAGGTGAGCGGCCCAGAGTTAACGGGGG CTTCCGCCTCCCTGAGGACCAAGCTGTCATTAGCAGGTAGGTGAGCGGCCCAGAGTTAACGGGGG A G DHODH Ensembl:ENSG00000102967 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:72014618..72015718 32194978 MeRIP-seq:(Medium) rs1215774893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5360855,Human_RBP_ID_17880669 Human_Splice_Rec_1738351,Human_Splice_Rec_1738365,Human_Splice_Rec_1738379,Human_Splice_Rec_1738389,Human_Splice_Rec_1738397,Human_Splice_Rec_1738401,Human_Splice_Rec_1738405,Human_Splice_Rec_1738411 RMVar_hsa_circ_179867,RMVar_hsa_circ_118880,RMVar_hsa_circ_179868,RMVar_hsa_circ_121964 93164 RMVar_ID_93164 Human_SNP_ID_607912946 m1A Human chr16 + 72021055 72021055 72021055 GGCCTGCGCGGCTGTCCACAGGTGGTTTGGTCAAGGGCAGCCTCAGAAGGTGGCACAGGAAAGGG GGCCTGCGCGGCTGTCCACAGGTGGTTTGGTCGAGGGCAGCCTCAGAAGGTGGCACAGGAAAGGG A G DHODH Ensembl:ENSG00000102967 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:72021041..72021113 26863196 MeRIP-seq:(Medium) rs559542296 Functional Loss SNV dbSNP153 33..33 33 - - - 93165 RMVar_ID_93165 Human_SNP_ID_607913037 m1A Human chr16 - 72021217 72021216 72021217 GGCTGGACACATTCACCACCAGGTAGTCGGCCAGGGGGCCCAGTACGCGCACCCCTTCTGCGTAG GGCTGGACACATTCACCACCAGGTAGTCGGCC_GGGGGCCCAGTACGCGCACCCCTTCTGCGTAG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72021170..72021245 26863196 MeRIP-seq:(Medium) rs1215488320 Functional Loss DEL dbSNP153 33..33 33 - - - 93166 RMVar_ID_93166 Human_SNP_ID_607913818 m1A Human chr16 - 72023579 72023579 72023579 GCTTGACTTTGCCCACAACGGGTGGCCCCCAGAAGGTGAGGGCCGTGTACAGCTGCACCAGGGAG GCTTGACTTTGCCCACAACGGGTGGCCCCCAGCAGGTGAGGGCCGTGTACAGCTGCACCAGGGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:72023218..72024328 32194978 MeRIP-seq:(Medium) rs1424609724 Functional Loss SNV dbSNP153 33..33 33 - - - 93167 RMVar_ID_93167 Human_SNP_ID_607914042 m1A Human chr16 + 72024329 72024329 72024329 ATGTCCCCCAGCCATGGCATGGCTGCACTGTAAACGCCAATCGGGGGGTCACCAGGATCAACCGC ATGTCCCCCAGCCATGGCATGGCTGCACTGTAGACGCCAATCGGGGGGTCACCAGGATCAACCGC A G DHODH Ensembl:ENSG00000102967 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:72024278..72024428 32194978 MeRIP-seq:(Medium) rs1393173972 Functional Loss SNV dbSNP153 33..33 33 - - - 93168 RMVar_ID_93168 Human_SNP_ID_607934102 m1A Human chr16 + 72096920 72096920 72096920 ACGCAGTCGGCAGAGAGAGCGGGAGCGGCGGGAACATGGTGTCTATGCCTCGTCCAAAGAAGAAA ACGCAGTCGGCAGAGAGAGCGGGAGCGGCGGGGACATGGTGTCTATGCCTCGTCCAAAGAAGAAA A G DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:72096101..72097175;chr16:72093842..72097175;chr16:72093859..72097225 26863196 MeRIP-seq:(Medium) rs76109028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9285922,Human_RBP_ID_21889393,Human_RBP_ID_26329192,Human_RBP_ID_27811247 Human_Splice_Rec_1738634,Human_Splice_Rec_1738660,Human_Splice_Rec_1738661,Human_Splice_Rec_1738714,Human_Splice_Rec_1738715 RMVar_hsa_circ_53741 93169 RMVar_ID_93169 Human_SNP_ID_607934308 m1A Human chr16 + 72097629 72097629 72097629 GCCTGTCCTTTCTCTAGGGTGAAGATGTGTATACCTTAGGATGGGATGCATGTTTTTAAGCTTCG GCCTGTCCTTTCTCTAGGGTGAAGATGTGTATTCCTTAGGATGGGATGCATGTTTTTAAGCTTCG A T DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72097627..72097800 26863196 MeRIP-seq:(Medium) rs1354282568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23699098 RMVar_hsa_circ_53741 93170 RMVar_ID_93170 Human_SNP_ID_607934349 m1A Human chr16 - 72097727 72097727 72097727 CTCGGGTTCATTTCTTCTGCTGCTACGCTCTGACCCTCCATCTCGCTCTGATCTGCTGCTGTGCC CTCGGGTTCATTTCTTCTGCTGCTACGCTCTGCCCCTCCATCTCGCTCTGATCTGCTGCTGTGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72097618..72099084 26863196 MeRIP-seq:(Medium) rs776044870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18683859 93171 RMVar_ID_93171 Human_SNP_ID_607934658 m1A Human chr16 - 72098773 72098773 72098773 CCCAGAACATCACCTGTCTCGATCTCGAGTGGACAGCCGATGGCTCCGCTCAGAATCCCGATAGG CCCAGAACATCACCTGTCTCGATCTCGAGTGGCCAGCCGATGGCTCCGCTCAGAATCCCGATAGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:72097721..72099017 32194978 MeRIP-seq:(Medium) rs74649326 Functional Loss SNV dbSNP153 33..33 33 - - - 93172 RMVar_ID_93172 Human_SNP_ID_607934851 m1A Human chr16 + 72099267 72099267 72099267 ATTTGACACGGAGGAGGAGCGGCAGCAGTGGGAAGATGACCAGAGGGTAAAGTTTTATACCTCTG ATTTGACACGGAGGAGGAGCGGCAGCAGTGGGGAGATGACCAGAGGGTAAAGTTTTATACCTCTG A G DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:72099162..72099900;chr16:72097619..72100519 26863196 MeRIP-seq:(Medium) rs76047777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233714,Human_RBP_ID_818290,Human_RBP_ID_895682,Human_RBP_ID_8812050,Human_RBP_ID_9285925,Human_RBP_ID_9373168,Human_RBP_ID_18469801,Human_RBP_ID_18986912,Human_RBP_ID_22055189,Human_RBP_ID_24544417,Human_RBP_ID_26329196,Human_RBP_ID_27811250 Human_Splice_Rec_1738668,Human_Splice_Rec_1738669,Human_Splice_Rec_1738721,Human_Splice_Rec_1738728,Human_Splice_Rec_1738729 RMVar_hsa_circ_83109,RMVar_hsa_circ_106563,RMVar_hsa_circ_179873,RMVar_hsa_circ_179874,RMVar_hsa_circ_87519,RMVar_hsa_circ_179875 93173 RMVar_ID_93173 Human_SNP_ID_607934989 m1A Human chr16 - 72099690 72099690 72099690 AGGAGGCAAAGCAAGGGAGTGAGGGACAGATCAAGTTTATGCACGAGACATGGCCAACAGAAGAA AGGAGGCAAAGCAAGGGAGTGAGGGACAGATCGAGTTTATGCACGAGACATGGCCAACAGAAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72099688..72099907 26863196 MeRIP-seq:(Medium) rs765148055 Functional Loss SNV dbSNP153 33..33 33 - - - 93174 RMVar_ID_93174 Human_SNP_ID_607936322 m1A Human chr16 + 72103999 72103999 72103999 GAAGACTGCACTTCAGAGAACACCTTGATCAAATACATGACTGACGGGATCCTGCTCCGAGAGTC GAAGACTGCACTTCAGAGAACACCTTGATCAACTACATGACTGACGGGATCCTGCTCCGAGAGTC A C DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72103926..72104075 26863196 MeRIP-seq:(Medium) rs1437493098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9374624,Human_RBP_ID_18683869 Human_Splice_Rec_1738682,Human_Splice_Rec_1738740 RMVar_hsa_circ_38081,RMVar_hsa_circ_87519,RMVar_hsa_circ_179875,RMVar_hsa_circ_121473,RMVar_hsa_circ_179877 93175 RMVar_ID_93175 Human_SNP_ID_607936771 m1A Human chr16 + 72105254 72105254 72105254 GGGCTCTCAGGTGACCTCAGACCAGATTGTGGAGCATCTGGAGGAACTGGAGAACGCGCCTGCCC GGGCTCTCAGGTGACCTCAGACCAGATTGTGGCGCATCTGGAGGAACTGGAGAACGCGCCTGCCC A C DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:72104468..72105300 32194978 MeRIP-seq:(Medium) rs756701702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895592,Human_RBP_ID_1846194,Human_RBP_ID_6534668,Human_RBP_ID_8438427,Human_RBP_ID_8810165,Human_RBP_ID_17487665,Human_RBP_ID_18984237 Human_Splice_Rec_1738688,Human_Splice_Rec_1738689,Human_Splice_Rec_1738744,Human_Splice_Rec_1738745 Human_miRNA_ID_2071183,Human_miRNA_ID_2804109 RMVar_hsa_circ_38081,RMVar_hsa_circ_121473,RMVar_hsa_circ_18014,RMVar_hsa_circ_179877 93176 RMVar_ID_93176 Human_SNP_ID_607936772 m1A Human chr16 + 72105254 72105254 72105254 GGGCTCTCAGGTGACCTCAGACCAGATTGTGGAGCATCTGGAGGAACTGGAGAACGCGCCTGCCC GGGCTCTCAGGTGACCTCAGACCAGATTGTGGGGCATCTGGAGGAACTGGAGAACGCGCCTGCCC A G DHX38 Ensembl:ENSG00000140829 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:72104468..72105300 32194978 MeRIP-seq:(Medium) rs756701702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895592,Human_RBP_ID_1846194,Human_RBP_ID_6534668,Human_RBP_ID_8438427,Human_RBP_ID_8810165,Human_RBP_ID_17487665,Human_RBP_ID_18984237 Human_Splice_Rec_1738688,Human_Splice_Rec_1738689,Human_Splice_Rec_1738744,Human_Splice_Rec_1738745 Human_miRNA_ID_2071183,Human_miRNA_ID_2804109 RMVar_hsa_circ_38081,RMVar_hsa_circ_121473,RMVar_hsa_circ_18014,RMVar_hsa_circ_179877 93177 RMVar_ID_93177 Human_SNP_ID_608088824 m1A Human chr16 - 72664821 72664820 72664821 CGGAGCTGGAGGGGCGCGGAGTTAAACAAAAAAGGGCGGCCGGAGCTGCAGGGGCGCCGAGTTAA CGGAGCTGGAGGGGCGCGGAGTTAAACAAAAA_GGGCGGCCGGAGCTGCAGGGGCGCCGAGTTAA CT C LINC01572 Ensembl:ENSG00000261008 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:72664803..72664920 26863196 MeRIP-seq:(Medium) rs959505112 Functional Loss DEL dbSNP153 33..33 33 - - - 93178 RMVar_ID_93178 Human_SNP_ID_608089004 m1A Human chr16 - 72665237 72665237 72665237 AGGACACAGCCGGTGGAGGGACCCCAGCACACAGTCCCGTGGGTGCTCCGGAGGAAACGGCCGCA AGGACACAGCCGGTGGAGGGACCCCAGCACACCGTCCCGTGGGTGCTCCGGAGGAAACGGCCGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:72665188..72665326 26863196 MeRIP-seq:(Medium) rs1283969752 Functional Loss SNV dbSNP153 33..33 33 - - - 93179 RMVar_ID_93179 Human_SNP_ID_608122202 m1A Human chr16 + 72787719 72787695 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAG________________________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs765152994 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_9325207 93180 RMVar_ID_93180 Human_SNP_ID_608122210 m1A Human chr16 + 72787719 72787698 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCG_____________________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs781609559 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_9325207 93181 RMVar_ID_93181 Human_SNP_ID_608122220 m1A Human chr16 + 72787719 72787701 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCG__________________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs778016374 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_9325207 93182 RMVar_ID_93182 Human_SNP_ID_608122229 m1A Human chr16 + 72787719 72787704 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCG_______________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs771374165 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_9325207 93183 RMVar_ID_93183 Human_SNP_ID_608122234 m1A Human chr16 - 72787739 72787706 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC_________________________________ CGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs1567506139 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93184 RMVar_ID_93184 Human_SNP_ID_608122236 m1A Human chr16 + 72787719 72787707 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCG____________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs746268093 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_9325207 93185 RMVar_ID_93185 Human_SNP_ID_608122246 m1A Human chr16 + 72787719 72787710 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCGCCG_________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs760306096 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_9325207 93186 RMVar_ID_93186 Human_SNP_ID_608122253 m1A Human chr16 + 72787719 72787713 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCGCCGCCG______CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs761344900 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_9325207 93187 RMVar_ID_93187 Human_SNP_ID_608122260 m1A Human chr16 - 72787739 72787715 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC________________________GGCGGCGGC CGCCACCGCCGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs750348888 Functional Loss DEL dbSNP153,HGVD 33..56 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93188 RMVar_ID_93188 Human_SNP_ID_608122264 m1A Human chr16 + 72787737 72787716 72787737 CCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCCGCCGCCGGTGGGGACGTG CCGCCGCCGCCG_____________________CTGCCACCGCCGCCGCCGCCGGTGGGGACGTG GCCACCGCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:72787706..72787833 26863196 MeRIP-seq:(Medium) rs756410079 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_9325207 93189 RMVar_ID_93189 Human_SNP_ID_608122265 m1A Human chr16 + 72787719 72787716 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCGCCGCCGCCG___CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs766266415 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_9325207 93190 RMVar_ID_93190 Human_SNP_ID_608122272 m1A Human chr16 - 72787739 72787718 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC_____________________GGCGGCGGCGGC CACCGCCGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs778017973 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93191 RMVar_ID_93191 Human_SNP_ID_608122273 m1A Human chr16 + 72787719 72787719 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCACCGCCGCC A G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs112443847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9325207 93192 RMVar_ID_93192 Human_SNP_ID_608122286 m1A Human chr16 - 72787739 72787721 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC__________________GGTGGCGGCGGCGGC CGCCGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs775843921 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93193 RMVar_ID_93193 Human_SNP_ID_608122294 m1A Human chr16 - 72787739 72787724 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC_______________GGCGGTGGCGGCGGCGGC CGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs761275974 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93194 RMVar_ID_93194 Human_SNP_ID_608122305 m1A Human chr16 - 72787739 72787727 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC____________GGCGGCGGTGGCGGCGGCGGC CGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs1173189614 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93195 RMVar_ID_93195 Human_SNP_ID_608122315 m1A Human chr16 - 72787739 72787730 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC_________GGCGGCGGCGGTGGCGGCGGCGGC CGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs759356254 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93196 RMVar_ID_93196 Human_SNP_ID_608122324 m1A Human chr16 + 72787737 72787731 72787737 CCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCCGCCGCCGGTGGGGACGTG CCGCCGCCGCCGCCACCGCCGCCGCCG______CTGCCACCGCCGCCGCCGCCGGTGGGGACGTG GCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:72787706..72787833 26863196 MeRIP-seq:(Medium) rs757346850 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_9325207 93197 RMVar_ID_93197 Human_SNP_ID_608122331 m1A Human chr16 - 72787739 72787733 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC______GGCGGCGGCGGCGGTGGCGGCGGCGGC CGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs750444062 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93198 RMVar_ID_93198 Human_SNP_ID_608122335 m1A Human chr16 + 72787737 72787734 72787737 CCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCCGCCGCCGGTGGGGACGTG CCGCCGCCGCCGCCACCGCCGCCGCCGCCG___CTGCCACCGCCGCCGCCGCCGGTGGGGACGTG GCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:72787706..72787833 26863196 MeRIP-seq:(Medium) rs1567506504 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_9325207 93199 RMVar_ID_93199 Human_SNP_ID_608122339 m1A Human chr16 - 72787739 72787736 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC___GGCGGCGGCGGCGGCGGTGGCGGCGGCGGC CACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs1283843849 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93200 RMVar_ID_93200 Human_SNP_ID_608122340 m1A Human chr16 + 72787737 72787737 72787737 CCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCCGCCGCCGGTGGGGACGTG CCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCGCTGCCACCGCCGCCGCCGCCGGTGGGGACGTG A G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:72787706..72787833 26863196 MeRIP-seq:(Medium) rs544296333 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9325207 93201 RMVar_ID_93201 Human_SNP_ID_608122342 m1A Human chr16 - 72787739 72787737 72787740 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGG___TGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC ACTG A ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs1429156408 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93202 RMVar_ID_93202 Human_SNP_ID_608122350 m1A Human chr16 - 72787739 72787739 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCGGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC T C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs200561133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93203 RMVar_ID_93203 Human_SNP_ID_608122351 m1A Human chr16 - 72787739 72787739 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCCGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC T G ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs200561133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 93204 RMVar_ID_93204 Human_SNP_ID_608122545 m1A Human chr16 - 72788002 72788002 72788002 TGCCAAAGAATCCCCCAAACCAGAAGAACAGAAAAACACCCCCCGTGAGGTGTCCCCCCTCCTGC TGCCAAAGAATCCCCCAAACCAGAAGAACAGAGAAACACCCCCCGTGAGGTGTCCCCCCTCCTGC T C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:72787952..72788110 26863196 MeRIP-seq:(Medium) rs780948706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18940531 93205 RMVar_ID_93205 Human_SNP_ID_608122562 m1A Human chr16 - 72788028 72788028 72788028 GGGGCTCCTTCCCCAGACAAAGACCCTGCCAAAGAATCCCCCAAACCAGAAGAACAGAAAAACAC GGGGCTCCTTCCCCAGACAAAGACCCTGCCAACGAATCCCCCAAACCAGAAGAACAGAAAAACAC T G ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:72787977..72788111 26863196 MeRIP-seq:(Medium) rs1197736437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18940531 93206 RMVar_ID_93206 Human_SNP_ID_608122926 m1A Human chr16 + 72788646 72788584 72788647 GTGGGTGGCGGCTGGGCTGCTGGCGGCGGGGGAGGCTGCTGCACCTGTGGTTGCTGCTGCTGCTG __________________________________GCTGCTGCACCTGTGGTTGCTGCTGCTGCTG TGCTGCTGCTGTTGCAGTGGGAGCTGTGGTGTGGGTGGCGGCTGGGCTGCTGGCGGCGGGGGAG T AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:72788595..72788783 26863196 MeRIP-seq:(Medium) rs1567508890 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5141961,Human_RBP_ID_9353243,Human_RBP_ID_21971453,Human_RBP_ID_22474169 93207 RMVar_ID_93207 Human_SNP_ID_608122967 m1A Human chr16 + 72788646 72788646 72788646 GTGGGTGGCGGCTGGGCTGCTGGCGGCGGGGGAGGCTGCTGCACCTGTGGTTGCTGCTGCTGCTG GTGGGTGGCGGCTGGGCTGCTGGCGGCGGGGGGGGCTGCTGCACCTGTGGTTGCTGCTGCTGCTG A G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:72788595..72788783 26863196 MeRIP-seq:(Medium) rs995671051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5141961,Human_RBP_ID_9353243,Human_RBP_ID_21971453,Human_RBP_ID_22474169 93208 RMVar_ID_93208 Human_SNP_ID_608125089 m1A Human chr16 + 72795193 72795193 72795193 CAGGTGGGAGAGCTGGGAAGGACTGGGGCTCGACTGGGGTAAGGGGCACTGTGGAGGGGGCGCTT CAGGTGGGAGAGCTGGGAAGGACTGGGGCTCGCCTGGGGTAAGGGGCACTGTGGAGGGGGCGCTT A C AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:72795096..72795301 26863196 MeRIP-seq:(Medium) rs780252867 Functional Loss SNV dbSNP153 33..33 33 - - - 93209 RMVar_ID_93209 Human_SNP_ID_608125506 m1A Human chr16 + 72796401 72796401 72796401 TCGTCTGCATCATCAGCGGCGAGAAGATGGGCAGCTCCATCGGCATGGAGAGCTGGGTGAGCGGC TCGTCTGCATCATCAGCGGCGAGAAGATGGGCGGCTCCATCGGCATGGAGAGCTGGGTGAGCGGC A G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72796372..72796543 26863196 MeRIP-seq:(Medium) rs140314411 Functional Loss SNV dbSNP153 33..33 33 - - - 93210 RMVar_ID_93210 Human_SNP_ID_608150368 m1A Human chr16 + 72887791 72887791 72887791 GTGAGTGTATACAGGGGGTGTGTGTGTGTACAACGTATGTGGGTATGGTGTCTTGTCTGTGGGCT GTGAGTGTATACAGGGGGTGTGTGTGTGTACAGCGTATGTGGGTATGGTGTCTTGTCTGTGGGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72887789..72887872 26863196 MeRIP-seq:(Medium) rs1233835082 Functional Loss SNV dbSNP153 33..33 33 - - - 93211 RMVar_ID_93211 Human_SNP_ID_608171353 m1A Human chr16 - 72958623 72958623 72958623 CGAGTTGGATGAGGAACTGGAGGACAGGCCCCATGAGGAGCCTGGGGCCGCAGCAGGTAGTAGCA CGAGTTGGATGAGGAACTGGAGGACAGGCCCCGTGAGGAGCCTGGGGCCGCAGCAGGTAGTAGCA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:72958572..72958841;chr16:72958576..72958856 26863196 MeRIP-seq:(Medium) rs1449867919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_894506,Human_RBP_ID_5524655,Human_RBP_ID_5572037,Human_RBP_ID_8231677,Human_RBP_ID_27245717 RMVar_hsa_circ_26118,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011,RMVar_hsa_circ_294312,RMVar_hsa_circ_91300,RMVar_hsa_circ_112909,RMVar_hsa_circ_97467,RMVar_hsa_circ_179900,RMVar_hsa_circ_179901,RMVar_hsa_circ_270069,RMVar_hsa_circ_100227,RMVar_hsa_circ_179903,RMVar_hsa_circ_179904,RMVar_hsa_circ_179902,RMVar_hsa_circ_288691,RMVar_hsa_circ_179906,RMVar_hsa_circ_179907 93212 RMVar_ID_93212 Human_SNP_ID_608171835 m1A Human chr16 - 72959568 72959568 72959568 GGACCCTTCGTGTGCTGCACCCGTGTACCCGCAGATCATCAACACTTTCCACATAGCCTCATCCT GGACCCTTCGTGTGCTGCACCCGTGTACCCGCTGATCATCAACACTTTCCACATAGCCTCATCCT T A ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:72959526..72959682 26863196 MeRIP-seq:(Medium) rs766294787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5525099,Human_RBP_ID_17256774 RMVar_hsa_circ_26118,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011,RMVar_hsa_circ_294312,RMVar_hsa_circ_91300,RMVar_hsa_circ_112909,RMVar_hsa_circ_97467,RMVar_hsa_circ_179900,RMVar_hsa_circ_179901,RMVar_hsa_circ_270069,RMVar_hsa_circ_100227,RMVar_hsa_circ_179903,RMVar_hsa_circ_179904,RMVar_hsa_circ_179902,RMVar_hsa_circ_288691,RMVar_hsa_circ_179906,RMVar_hsa_circ_179907 93213 RMVar_ID_93213 Human_SNP_ID_608171836 m1A Human chr16 - 72959568 72959568 72959568 GGACCCTTCGTGTGCTGCACCCGTGTACCCGCAGATCATCAACACTTTCCACATAGCCTCATCCT GGACCCTTCGTGTGCTGCACCCGTGTACCCGCGGATCATCAACACTTTCCACATAGCCTCATCCT T C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:72959526..72959682 26863196 MeRIP-seq:(Medium) rs766294787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5525099,Human_RBP_ID_17256774 RMVar_hsa_circ_26118,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011,RMVar_hsa_circ_294312,RMVar_hsa_circ_91300,RMVar_hsa_circ_112909,RMVar_hsa_circ_97467,RMVar_hsa_circ_179900,RMVar_hsa_circ_179901,RMVar_hsa_circ_270069,RMVar_hsa_circ_100227,RMVar_hsa_circ_179903,RMVar_hsa_circ_179904,RMVar_hsa_circ_179902,RMVar_hsa_circ_288691,RMVar_hsa_circ_179906,RMVar_hsa_circ_179907 93214 RMVar_ID_93214 Human_SNP_ID_608188037 m1A Human chr16 + 73017487 73017487 73017487 GCTTTCCAGTGGTGCCCTTCGCCAAGTCATGAAAACTCTGCCAACACTGTTCTCTCTCCAGCACT GCTTTCCAGTGGTGCCCTTCGCCAAGTCATGAGAACTCTGCCAACACTGTTCTCTCTCCAGCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:73017484..73017567 26863196 MeRIP-seq:(Medium) rs954863597 Functional Loss SNV dbSNP153 33..33 33 - - - 93215 RMVar_ID_93215 Human_SNP_ID_608196810 m1A Human chr16 - 73047821 73047821 73047821 TCGGGTGCCACTGGAATTTCCCGTTGTTGCGCATGGCGGCGCGGCCCCCGGACCTGCAAGTGCCG TCGGGTGCCACTGGAATTTCCCGTTGTTGCGCGTGGCGGCGCGGCCCCCGGACCTGCAAGTGCCG T C ZFHX3 Ensembl:ENSG00000140836 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:73047771..73048092 26863196 MeRIP-seq:(Medium) rs1156757147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_894514,Human_RBP_ID_5181965,Human_RBP_ID_5524667,Human_RBP_ID_6536139,Human_RBP_ID_18459181,Human_RBP_ID_22697114,Human_RBP_ID_22714419 Human_Splice_Rec_1739225 RMVar_hsa_circ_26118,RMVar_hsa_circ_81898,RMVar_hsa_circ_179897,RMVar_hsa_circ_91300,RMVar_hsa_circ_112909,RMVar_hsa_circ_97467,RMVar_hsa_circ_179901,RMVar_hsa_circ_100227,RMVar_hsa_circ_179903,RMVar_hsa_circ_179902,RMVar_hsa_circ_179907 93216 RMVar_ID_93216 Human_SNP_ID_608197215 m1A Human chr16 + 73049102 73049102 73049102 TCTCCCCAAGTTCACCTTTTCCAGTTGGTCAAAGCGATTGCTGGGCGCCTTCTATCTCCCCAAGT TCTCCCCAAGTTCACCTTTTCCAGTTGGTCAATGCGATTGCTGGGCGCCTTCTATCTCCCCAAGT A T lnc-DHX38-29,lnc-DHX38-29:2,lnc-DHX38-29:3 RNACentral:URS0000D5B1B8,RNACentral:URS0000D5CFF7,RNACentral:URS0000D58D9C lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:73049100..73049284 26863196 MeRIP-seq:(Medium) rs1298502536 Functional Loss SNV dbSNP153 33..33 33 - - - 93217 RMVar_ID_93217 Human_SNP_ID_608197222 m1A Human chr16 - 73049119 73049119 73049119 AGAATGGAAAAAGGTGGACTTGGGGAGATAGAAGGCGCCCAGCAATCGCTTTGACCAACTGGAAA AGAATGGAAAAAGGTGGACTTGGGGAGATAGAGGGCGCCCAGCAATCGCTTTGACCAACTGGAAA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:73049117..73049282 26863196 MeRIP-seq:(Medium) rs974810329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26118,RMVar_hsa_circ_81898,RMVar_hsa_circ_179897,RMVar_hsa_circ_100227,RMVar_hsa_circ_179902 93218 RMVar_ID_93218 Human_SNP_ID_608201936 m1A Human chr16 + 73064188 73064188 73064188 AAAGGGAACTAGATCCCTGGGGGGCAGGAGGCAGGTGGGGGGTGCGGTGAGAAGATAAGGAGATG AAAGGGAACTAGATCCCTGGGGGGCAGGAGGCGGGTGGGGGGTGCGGTGAGAAGATAAGGAGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:73064155..73064243 26863196 MeRIP-seq:(Medium) rs1299593383 Functional Loss SNV dbSNP153 33..33 33 - - - 93219 RMVar_ID_93219 Human_SNP_ID_608558220 m1A Human chr16 + 74305668 74305629 74305668 AAGAAGAGAGCAAAAAGGATAGGAAAGAGGACAAGGAGAAAGATAAAGATAAGGAAAAGAGTGAT _________________________________AGGAGAAAGATAAAGATAAGGAAAAGAGTGAT CAGGAGAAAGAAGAGAGCAAAAAGGATAGGAAAGAGGACA C PSMD7 Ensembl:ENSG00000103035 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:74305557..74305750 26863196 MeRIP-seq:(Medium) rs1567526813 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_44134,Human_RBP_ID_8438768,Human_RBP_ID_18411407,Human_RBP_ID_18529877,Human_RBP_ID_23699734,Human_RBP_ID_24544542,Human_RBP_ID_26329215 Human_miRNA_ID_1191928,Human_miRNA_ID_2255421,Human_miRNA_ID_2571189,Human_miRNA_ID_3044925 RMVar_hsa_circ_101025,RMVar_hsa_circ_92508,RMVar_hsa_circ_179910,RMVar_hsa_circ_89829,RMVar_hsa_circ_179912,RMVar_hsa_circ_82589,RMVar_hsa_circ_179913,RMVar_hsa_circ_179917,RMVar_hsa_circ_76646,RMVar_hsa_circ_94310,RMVar_hsa_circ_179919,RMVar_hsa_circ_117663,RMVar_hsa_circ_179921,RMVar_hsa_circ_179922 93220 RMVar_ID_93220 Human_SNP_ID_608558239 m1A Human chr16 + 74305678 74305673 74305679 CAAAAAGGATAGGAAAGAGGACAAGGAGAAAGATAAAGATAAGGAAAAGAGTGATGTAAAGAAAG CAAAAAGGATAGGAAAGAGGACAAGGAG______AAAGATAAGGAAAAGAGTGATGTAAAGAAAG GAAAGAT G PSMD7 Ensembl:ENSG00000103035 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:74305545..74305775;chr16:74305565..74305750 26863196 MeRIP-seq:(Medium) rs776195019 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_44134,Human_RBP_ID_8438768,Human_RBP_ID_18411407,Human_RBP_ID_18529878,Human_RBP_ID_23699734,Human_RBP_ID_26329216 RMVar_hsa_circ_101025,RMVar_hsa_circ_92508,RMVar_hsa_circ_179910,RMVar_hsa_circ_89829,RMVar_hsa_circ_179912,RMVar_hsa_circ_82589,RMVar_hsa_circ_179913,RMVar_hsa_circ_179917,RMVar_hsa_circ_76646,RMVar_hsa_circ_94310,RMVar_hsa_circ_179919,RMVar_hsa_circ_117663,RMVar_hsa_circ_179921,RMVar_hsa_circ_179922 93221 RMVar_ID_93221 Human_SNP_ID_608562551 m1A Human chr16 - 74319340 74319339 74319341 GATCCATAGGTTGGTGCAGGTCCAGGTCATGCAGGGACCCGTGAGCCCCGATGAAGAGCTTGGGT GATCCATAGGTTGGTGCAGGTCCAGGTCATG__GGGACCCGTGAGCCCCGATGAAGAGCTTGGGT CTG C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:74319162..74319359 26863196 MeRIP-seq:(Medium) rs1487642688 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_198065,Human_RBP_ID_888938,Human_RBP_ID_22356165,Human_RBP_ID_22523449,Human_RBP_ID_22712246,Human_RBP_ID_22944477,Human_RBP_ID_23118488,Human_RBP_ID_24544614,Human_RBP_ID_26329223,Human_RBP_ID_27572573 93222 RMVar_ID_93222 Human_SNP_ID_608562610 m1A Human chr16 - 74319523 74319515 74319523 AGAAGAAGAAAGAAGGAGAAGGAAAGAAAGAAAGAAAGAAGAATCAGCCAGCCAAGTAAAGAGCT AGAAGAAGAAAGAAGGAGAAGGAAAGAAAGAA________GAATCAGCCAGCCAAGTAAAGAGCT CTTCTTTCT C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74319400..74319644 26863196 MeRIP-seq:(Medium) rs371812896 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_892576,Human_RBP_ID_1526928,Human_RBP_ID_5096753,Human_RBP_ID_5247751 93223 RMVar_ID_93223 Human_SNP_ID_608562611 m1A Human chr16 - 74319523 74319515 74319523 AGAAGAAGAAAGAAGGAGAAGGAAAGAAAGAAAGAAAGAAGAATCAGCCAGCCAAGTAAAGAGCT AGAAGAAGAAAGAAGGAGAAGGAAAGAAAGAA____AGAAGAATCAGCCAGCCAAGTAAAGAGCT CTTCTTTCT CTTCT AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74319400..74319644 26863196 MeRIP-seq:(Medium) rs371812896 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_892576,Human_RBP_ID_1526928,Human_RBP_ID_5096753,Human_RBP_ID_5247751 93224 RMVar_ID_93224 Human_SNP_ID_608562639 m1A Human chr16 - 74319557 74319555 74319558 GAAAGGAGGAGGAGGAGGAGGAGAAGGAGAAGAAAGAAGAAGAAAGAAGGAGAAGGAAAGAAAGA GAAAGGAGGAGGAGGAGGAGGAGAAGGAGAA___AGAAGAAGAAAGAAGGAGAAGGAAAGAAAGA TTTC T AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:74319348..74319609 26863196 MeRIP-seq:(Medium) rs953209858 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_892576,Human_RBP_ID_1526928,Human_RBP_ID_5096753,Human_RBP_ID_5247751,Human_RBP_ID_22356166,Human_RBP_ID_24544544 93225 RMVar_ID_93225 Human_SNP_ID_608566756 m1A Human chr16 + 74331567 74331567 74331567 TCTCAAAAGTACAAATACTTAAAAAAAAAAAAAAAAACTACTCAAAAATTACCTGGGGCCAGGCA TCTCAAAAGTACAAATACTTAAAAAAAAAAAACAAAACTACTCAAAAATTACCTGGGGCCAGGCA A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:74331557..74331646 26863410 MeRIP-seq:(Medium) rs979756928 Functional Loss SNV dbSNP153 33..33 33 - - - 93226 RMVar_ID_93226 Human_SNP_ID_608577029 m1A Human chr16 - 74360773 74360773 74360773 TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCATCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCTTCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC T A AC009053.2 Ensembl:ENSG00000214331 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62055171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510562,Human_RBP_ID_5096542,Human_RBP_ID_9373210,Human_RBP_ID_18529945,Human_RBP_ID_24371089 RMVar_hsa_circ_377905,RMVar_hsa_circ_107349,RMVar_hsa_circ_179924,RMVar_hsa_circ_295646,RMVar_hsa_circ_179928,RMVar_hsa_circ_179927,RMVar_hsa_circ_330711,RMVar_hsa_circ_19145,RMVar_hsa_circ_352828,RMVar_hsa_circ_358935,RMVar_hsa_circ_179933,RMVar_hsa_circ_179932,RMVar_hsa_circ_292513,RMVar_hsa_circ_303550 93227 RMVar_ID_93227 Human_SNP_ID_608577030 m1A Human chr16 - 74360773 74360773 74360773 TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCATCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCGTCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62055171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510562,Human_RBP_ID_5096542,Human_RBP_ID_9373210,Human_RBP_ID_18529945,Human_RBP_ID_24371089 RMVar_hsa_circ_377905,RMVar_hsa_circ_107349,RMVar_hsa_circ_179924,RMVar_hsa_circ_295646,RMVar_hsa_circ_179928,RMVar_hsa_circ_179927,RMVar_hsa_circ_330711,RMVar_hsa_circ_19145,RMVar_hsa_circ_352828,RMVar_hsa_circ_358935,RMVar_hsa_circ_179933,RMVar_hsa_circ_179932,RMVar_hsa_circ_292513,RMVar_hsa_circ_303550 93228 RMVar_ID_93228 Human_SNP_ID_608577883 m1A Human chr16 - 74362927 74362927 74362927 TTGAAGGTTGAGAGAGGAATAGCTGGGCTCTGAACCTGAATACAGACAGAGGTCTACCTGTGGCT TTGAAGGTTGAGAGAGGAATAGCTGGGCTCTGGACCTGAATACAGACAGAGGTCTACCTGTGGCT T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:74362880..74363246 26863196 MeRIP-seq:(Medium) rs565887033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5572941,Human_RBP_ID_18926619 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 93229 RMVar_ID_93229 Human_SNP_ID_608577924 m1A Human chr16 + 74363052 74363052 74363052 CCCTTCCTATAGACCCACTTACATCTGCAACCATCTCTTCCTTCTTTTATCCACTGGAAAGTTAA CCCTTCCTATAGACCCACTTACATCTGCAACCGTCTCTTCCTTCTTTTATCCACTGGAAAGTTAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:74363028..74363270 26863196 MeRIP-seq:(Medium) rs1384751331 Functional Loss SNV dbSNP153 33..33 33 - - - 93230 RMVar_ID_93230 Human_SNP_ID_608609158 m1A Human chr16 + 74452562 74452562 74452562 AACTGGAAAGCGTCACTGTCTCAGCAGAAGAAAGCAGGACCCCACACAGCCTGGGGAACGGCTGC AACTGGAAAGCGTCACTGTCTCAGCAGAAGAAGGCAGGACCCCACACAGCCTGGGGAACGGCTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:74452512..74452712 32194978 MeRIP-seq:(Medium) rs1328697088 Functional Loss SNV dbSNP153 33..33 33 - - - 93231 RMVar_ID_93231 Human_SNP_ID_608609309 m1A Human chr16 - 74453001 74453001 74453001 TGCGTTGTCCCATCCAGCCTCCACTCGTGTCCATGGTGTCCTCCTCCTCCTCACCGTGCAGCAGC TGCGTTGTCCCATCCAGCCTCCACTCGTGTCCGTGGTGTCCTCCTCCTCCTCACCGTGCAGCAGC T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74452913..74453122 26863196 MeRIP-seq:(Medium) rs114491569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479460,Human_RBP_ID_17256795,Human_RBP_ID_17488470,Human_RBP_ID_26949292 Human_miRNA_ID_189505,Human_miRNA_ID_1959503 RMVar_hsa_circ_100317,RMVar_hsa_circ_121633,RMVar_hsa_circ_179934,RMVar_hsa_circ_179935 93232 RMVar_ID_93232 Human_SNP_ID_608612746 m1A Human chr16 - 74463414 74463414 74463414 TTGCAGTGCTTGAAGCAAAATAAAAACAGTGAATTGATGGATCCCAAATGCAAACAGATGATAAC TTGCAGTGCTTGAAGCAAAATAAAAACAGTGAGTTGATGGATCCCAAATGCAAACAGATGATAAC T C GLG1 Ensembl:ENSG00000090863 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74463363..74465710 32194978 MeRIP-seq:(Medium) rs200712036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1846503,Human_RBP_ID_12809485 Human_Splice_Rec_1739862,Human_Splice_Rec_1739863,Human_Splice_Rec_1739914,Human_Splice_Rec_1739915,Human_Splice_Rec_1739962,Human_Splice_Rec_1739963,Human_Splice_Rec_1740004,Human_Splice_Rec_1740005,Human_Splice_Rec_1740056,Human_Splice_Rec_1740057,Human_Splice_Rec_1740076,Human_Splice_Rec_1740079 Human_miRNA_ID_3063281 RMVar_hsa_circ_20809,RMVar_hsa_circ_121633,RMVar_hsa_circ_179935,RMVar_hsa_circ_23793,RMVar_hsa_circ_54318,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_67270,RMVar_hsa_circ_75482,RMVar_hsa_circ_64890,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_179940,RMVar_hsa_circ_11610,RMVar_hsa_circ_179944,RMVar_hsa_circ_115672,RMVar_hsa_circ_305269,RMVar_hsa_circ_321638,RMVar_hsa_circ_345084,RMVar_hsa_circ_292548,RMVar_hsa_circ_179946,RMVar_hsa_circ_179945,RMVar_hsa_circ_297579,RMVar_hsa_circ_179942,RMVar_hsa_circ_179943,RMVar_hsa_circ_323969,RMVar_hsa_circ_318392,RMVar_hsa_circ_276518,RMVar_hsa_circ_294160,RMVar_hsa_circ_104398,RMVar_hsa_circ_179951,RMVar_hsa_circ_179952,RMVar_hsa_circ_179953,RMVar_hsa_circ_179950,RMVar_hsa_circ_27971,RMVar_hsa_circ_29687,RMVar_hsa_circ_22097,RMVar_hsa_circ_357120,RMVar_hsa_circ_11749,RMVar_hsa_circ_24809,RMVar_hsa_circ_340694,RMVar_hsa_circ_179954 93233 RMVar_ID_93233 Human_SNP_ID_608612752 m1A Human chr16 - 74463449 74463449 74463449 AGAGGTTCTGTCCGGAAGCAGATTCTAAAACCATGTTGCAGTGCTTGAAGCAAAATAAAAACAGT AGAGGTTCTGTCCGGAAGCAGATTCTAAAACCGTGTTGCAGTGCTTGAAGCAAAATAAAAACAGT T C GLG1 Ensembl:ENSG00000090863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74463400..74463523 26863196 MeRIP-seq:(Medium) rs575198253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43927,Human_RBP_ID_888941,Human_RBP_ID_1846503,Human_RBP_ID_4403468,Human_RBP_ID_17690813,Human_RBP_ID_17883569,Human_RBP_ID_23699844,Human_RBP_ID_25228685 Human_Splice_Rec_1739862,Human_Splice_Rec_1739863,Human_Splice_Rec_1739914,Human_Splice_Rec_1739915,Human_Splice_Rec_1739962,Human_Splice_Rec_1739963,Human_Splice_Rec_1740004,Human_Splice_Rec_1740005,Human_Splice_Rec_1740056,Human_Splice_Rec_1740057,Human_Splice_Rec_1740076,Human_Splice_Rec_1740079 Human_miRNA_ID_2742968 RMVar_hsa_circ_20809,RMVar_hsa_circ_121633,RMVar_hsa_circ_179935,RMVar_hsa_circ_23793,RMVar_hsa_circ_54318,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_67270,RMVar_hsa_circ_75482,RMVar_hsa_circ_64890,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_179940,RMVar_hsa_circ_11610,RMVar_hsa_circ_179944,RMVar_hsa_circ_115672,RMVar_hsa_circ_305269,RMVar_hsa_circ_321638,RMVar_hsa_circ_345084,RMVar_hsa_circ_292548,RMVar_hsa_circ_179946,RMVar_hsa_circ_179945,RMVar_hsa_circ_297579,RMVar_hsa_circ_179942,RMVar_hsa_circ_179943,RMVar_hsa_circ_323969,RMVar_hsa_circ_318392,RMVar_hsa_circ_276518,RMVar_hsa_circ_294160,RMVar_hsa_circ_104398,RMVar_hsa_circ_179951,RMVar_hsa_circ_179952,RMVar_hsa_circ_179953,RMVar_hsa_circ_179950,RMVar_hsa_circ_27971,RMVar_hsa_circ_29687,RMVar_hsa_circ_22097,RMVar_hsa_circ_357120,RMVar_hsa_circ_11749,RMVar_hsa_circ_24809,RMVar_hsa_circ_340694,RMVar_hsa_circ_179954 93234 RMVar_ID_93234 Human_SNP_ID_608613523 m1A Human chr16 - 74465777 74465777 74465777 TCGAATGTCTGAAAGAAAACAAGAAGCAGCTAAGCACCCGCTGCCACCAAAAAGTATTTAAGCTG TCGAATGTCTGAAAGAAAACAAGAAGCAGCTAGGCACCCGCTGCCACCAAAAAGTATTTAAGCTG T C GLG1 Ensembl:ENSG00000090863 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:74465618..74465843 26863196 MeRIP-seq:(Medium) rs1319225479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22760593 Human_Splice_Rec_1739860,Human_Splice_Rec_1739912,Human_Splice_Rec_1739960,Human_Splice_Rec_1740002,Human_Splice_Rec_1740054,Human_Splice_Rec_1740074 Human_miRNA_ID_182418 RMVar_hsa_circ_20809,RMVar_hsa_circ_121633,RMVar_hsa_circ_179935,RMVar_hsa_circ_23793,RMVar_hsa_circ_54318,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_67270,RMVar_hsa_circ_75482,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_11610,RMVar_hsa_circ_179944,RMVar_hsa_circ_115672,RMVar_hsa_circ_321638,RMVar_hsa_circ_345084,RMVar_hsa_circ_292548,RMVar_hsa_circ_179945,RMVar_hsa_circ_297579,RMVar_hsa_circ_179942,RMVar_hsa_circ_179943,RMVar_hsa_circ_323969,RMVar_hsa_circ_318392,RMVar_hsa_circ_294160,RMVar_hsa_circ_104398,RMVar_hsa_circ_179951,RMVar_hsa_circ_179952,RMVar_hsa_circ_179953,RMVar_hsa_circ_27971,RMVar_hsa_circ_29687,RMVar_hsa_circ_96558,RMVar_hsa_circ_11749,RMVar_hsa_circ_24809,RMVar_hsa_circ_340694,RMVar_hsa_circ_179954,RMVar_hsa_circ_348785,RMVar_hsa_circ_15226,RMVar_hsa_circ_60359,RMVar_hsa_circ_179955 93235 RMVar_ID_93235 Human_SNP_ID_608625701 m1A Human chr16 - 74503726 74503726 74503726 TATTTTGAGCAGATTAAAGAATGTGCTGATGAACCGGTTGGAAAAGGTTACATGGTTTCCTGCTT TATTTTGAGCAGATTAAAGAATGTGCTGATGAGCCGGTTGGAAAAGGTTACATGGTTTCCTGCTT T C GLG1 Ensembl:ENSG00000090863 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74503626..74503726 32194978 MeRIP-seq:(Medium) rs1177494258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1846523,Human_RBP_ID_18684414,Human_RBP_ID_23699881 Human_Splice_Rec_1739830,Human_Splice_Rec_1739882,Human_Splice_Rec_1739930,Human_Splice_Rec_1739982,Human_Splice_Rec_1740022,Human_Splice_Rec_1740100,Human_Splice_Rec_1740128,Human_Splice_Rec_1740136 Human_miRNA_ID_2560301,Human_miRNA_ID_2584420,Human_miRNA_ID_3002771 RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_66790,RMVar_hsa_circ_67380,RMVar_hsa_circ_358004,RMVar_hsa_circ_108207,RMVar_hsa_circ_179963,RMVar_hsa_circ_342637,RMVar_hsa_circ_345792,RMVar_hsa_circ_359220,RMVar_hsa_circ_55149,RMVar_hsa_circ_316303,RMVar_hsa_circ_179966,RMVar_hsa_circ_179967,RMVar_hsa_circ_311608,RMVar_hsa_circ_362182,RMVar_hsa_circ_69784 93236 RMVar_ID_93236 Human_SNP_ID_608658409 m1A Human chr16 + 74606777 74606777 74606777 GACTCTTCCTCCGCCAGCTTCCAGCCCCCACCAGCCCCCGCTCCTCCCCGCCGGGCCGGAGGCCC GACTCTTCCTCCGCCAGCTTCCAGCCCCCACCCGCCCCCGCTCCTCCCCGCCGGGCCGGAGGCCC A C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74606726..74606805 26863196 MeRIP-seq:(Medium) rs771470230 Functional Loss SNV dbSNP153 33..33 33 - - - 93237 RMVar_ID_93237 Human_SNP_ID_608658410 m1A Human chr16 + 74606777 74606777 74606777 GACTCTTCCTCCGCCAGCTTCCAGCCCCCACCAGCCCCCGCTCCTCCCCGCCGGGCCGGAGGCCC GACTCTTCCTCCGCCAGCTTCCAGCCCCCACCTGCCCCCGCTCCTCCCCGCCGGGCCGGAGGCCC A T RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74606726..74606805 26863196 MeRIP-seq:(Medium) rs771470230 Functional Loss SNV dbSNP153 33..33 33 - - - 93238 RMVar_ID_93238 Human_SNP_ID_608668610 m1A Human chr16 - 74637884 74637884 74637884 GTGCCGACTCCAACTGCAGGTCCTCACTGATAAGTGCACTAGGCTTCAAAGGCGTGTTCAGGTAC GTGCCGACTCCAACTGCAGGTCCTCACTGATACGTGCACTAGGCTTCAAAGGCGTGTTCAGGTAC T G RFWD3 Ensembl:ENSG00000168411 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74637851..74637975 32194978 MeRIP-seq:(Medium) rs1405792931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1740148,Human_Splice_Rec_1740149,Human_Splice_Rec_1740174,Human_Splice_Rec_1740175,Human_Splice_Rec_1740196 Human_miRNA_ID_2525523 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_81650,RMVar_hsa_circ_179972,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_179975,RMVar_hsa_circ_310100,RMVar_hsa_circ_336224,RMVar_hsa_circ_179977,RMVar_hsa_circ_179979,RMVar_hsa_circ_373538,RMVar_hsa_circ_124944,RMVar_hsa_circ_28231,RMVar_hsa_circ_179981,RMVar_hsa_circ_90685,RMVar_hsa_circ_299985,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179984,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_294256,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179990,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179992 93239 RMVar_ID_93239 Human_SNP_ID_608689138 m1A Human chr16 - 74700524 74700524 74700524 TCTCGCCTGGGCAGGAGGCGGTCGTGGGAAAGAAGGTGGAAGAGCGAGCTTTTTGGAACTGTGCA TCTCGCCTGGGCAGGAGGCGGTCGTGGGAAAGTAGGTGGAAGAGCGAGCTTTTTGGAACTGTGCA T A MLKL Ensembl:ENSG00000168404 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74695717..74700921 26863196 MeRIP-seq:(Medium) rs1025298024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1740229,Human_Splice_Rec_1740237,Human_Splice_Rec_1740280,Human_Splice_Rec_1740281,Human_Splice_Rec_1740285 RMVar_hsa_circ_94784,RMVar_hsa_circ_180003 93240 RMVar_ID_93240 Human_SNP_ID_608689139 m1A Human chr16 - 74700526 74700526 74700526 CTTCTCGCCTGGGCAGGAGGCGGTCGTGGGAAAGAAGGTGGAAGAGCGAGCTTTTTGGAACTGTG CTTCTCGCCTGGGCAGGAGGCGGTCGTGGGAAGGAAGGTGGAAGAGCGAGCTTTTTGGAACTGTG T C MLKL Ensembl:ENSG00000168404 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:74700476..74700677 26863196 MeRIP-seq:(Medium) rs974160952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1740229,Human_Splice_Rec_1740237,Human_Splice_Rec_1740280,Human_Splice_Rec_1740281,Human_Splice_Rec_1740285 RMVar_hsa_circ_94784,RMVar_hsa_circ_180003 93241 RMVar_ID_93241 Human_SNP_ID_608710276 m1A Human chr16 + 74774722 74774722 74774722 GGCCGCCAGGCGCCGCTGGACCTCGGAGGGCGAGAAGGAGGCGGCGGGGGGCGGAGCGGGGGCCA GGCCGCCAGGCGCCGCTGGACCTCGGAGGGCGTGAAGGAGGCGGCGGGGGGCGGAGCGGGGGCCA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:74774635..74774787 26863410 MeRIP-seq:(Medium) rs993939257 Functional Loss SNV dbSNP153 33..33 33 - - - 93242 RMVar_ID_93242 Human_SNP_ID_608739511 m1A Human chr16 - 74873854 74873853 74873854 CCCTGTAAGGTGTTAGCCTTAAACCACCGAGCAGCGTTCTCTTGATGCCAGTGCAGAGACCAGAG CCCTGTAAGGTGTTAGCCTTAAACCACCGAGC_GCGTTCTCTTGATGCCAGTGCAGAGACCAGAG CT C WDR59 Ensembl:ENSG00000103091 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74873659..74873859 32194978 MeRIP-seq:(Medium) rs1320673469 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5113643,Human_RBP_ID_18163619,Human_RBP_ID_18684525 RMVar_hsa_circ_180006,RMVar_hsa_circ_90270 93243 RMVar_ID_93243 Human_SNP_ID_608740120 m1A Human chr16 - 74875655 74875655 74875655 TTCAGGTTGGCCAAAGGGCAAATTGCAGCTAGAAAGGGGCAGGTGGACTGAAGGGTTAGTGGTGA TTCAGGTTGGCCAAAGGGCAAATTGCAGCTAGCAAGGGGCAGGTGGACTGAAGGGTTAGTGGTGA T G WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:74875650..74875715 26863196 MeRIP-seq:(Medium) rs1272616283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180006,RMVar_hsa_circ_90270 93244 RMVar_ID_93244 Human_SNP_ID_608742718 m1A Human chr16 - 74884935 74884935 74884935 AAACAGAAACGATGTGGGGGCAGGGAGAACAGAGAGGGAGAATCTTAGAAGAGGAATTGAGGTGT AAACAGAAACGATGTGGGGGCAGGGAGAACAGCGAGGGAGAATCTTAGAAGAGGAATTGAGGTGT T G WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:74884884..74884959 26863196 MeRIP-seq:(Medium) rs1174338534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180006,RMVar_hsa_circ_90270 93245 RMVar_ID_93245 Human_SNP_ID_608744356 m1A Human chr16 - 74889795 74889795 74889795 TGATCTGTCCAGGTTTGGTCGCTGGCTACGGTAGCTACAGATCTTTGCCTTGGTCCGAAATCTGA TGATCTGTCCAGGTTTGGTCGCTGGCTACGGTTGCTACAGATCTTTGCCTTGGTCCGAAATCTGA T A WDR59 Ensembl:ENSG00000103091 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74889748..74889851 26863196 MeRIP-seq:(Medium) rs771002476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12812308,Human_RBP_ID_18984275 Human_Splice_Rec_1740358,Human_Splice_Rec_1740359,Human_Splice_Rec_1740390,Human_Splice_Rec_1740391,Human_Splice_Rec_1740398,Human_Splice_Rec_1740399,Human_Splice_Rec_1740406,Human_Splice_Rec_1740422,Human_Splice_Rec_1740430 RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_310259,RMVar_hsa_circ_348093,RMVar_hsa_circ_364614,RMVar_hsa_circ_335991,RMVar_hsa_circ_301284,RMVar_hsa_circ_42922,RMVar_hsa_circ_6043,RMVar_hsa_circ_69206,RMVar_hsa_circ_180008,RMVar_hsa_circ_180009,RMVar_hsa_circ_275522,RMVar_hsa_circ_34028,RMVar_hsa_circ_268663,RMVar_hsa_circ_180010,RMVar_hsa_circ_286252,RMVar_hsa_circ_306088 93246 RMVar_ID_93246 Human_SNP_ID_608744357 m1A Human chr16 - 74889795 74889795 74889795 TGATCTGTCCAGGTTTGGTCGCTGGCTACGGTAGCTACAGATCTTTGCCTTGGTCCGAAATCTGA TGATCTGTCCAGGTTTGGTCGCTGGCTACGGTGGCTACAGATCTTTGCCTTGGTCCGAAATCTGA T C WDR59 Ensembl:ENSG00000103091 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74889748..74889851 26863196 MeRIP-seq:(Medium) rs771002476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12812308,Human_RBP_ID_18984275 Human_Splice_Rec_1740358,Human_Splice_Rec_1740359,Human_Splice_Rec_1740390,Human_Splice_Rec_1740391,Human_Splice_Rec_1740398,Human_Splice_Rec_1740399,Human_Splice_Rec_1740406,Human_Splice_Rec_1740422,Human_Splice_Rec_1740430 RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_310259,RMVar_hsa_circ_348093,RMVar_hsa_circ_364614,RMVar_hsa_circ_335991,RMVar_hsa_circ_301284,RMVar_hsa_circ_42922,RMVar_hsa_circ_6043,RMVar_hsa_circ_69206,RMVar_hsa_circ_180008,RMVar_hsa_circ_180009,RMVar_hsa_circ_275522,RMVar_hsa_circ_34028,RMVar_hsa_circ_268663,RMVar_hsa_circ_180010,RMVar_hsa_circ_286252,RMVar_hsa_circ_306088 93247 RMVar_ID_93247 Human_SNP_ID_608759169 m1A Human chr16 - 74938247 74938247 74938247 TGATCTGTTGCAGAAACCCAGTACAGCAGTGGAATATCTAGCCGCCCACCTCTCCAAAATCCATG TGATCTGTTGCAGAAACCCAGTACAGCAGTGGGATATCTAGCCGCCCACCTCTCCAAAATCCATG T C WDR59 Ensembl:ENSG00000103091 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74923965..74942757 32194978 MeRIP-seq:(Medium) rs372389250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9373235,Human_RBP_ID_22654495 Human_Splice_Rec_1740332,Human_Splice_Rec_1740333,Human_Splice_Rec_1740450,Human_Splice_Rec_1740451,Human_Splice_Rec_1740500,Human_Splice_Rec_1740501,Human_Splice_Rec_1740532,Human_Splice_Rec_1740533,Human_Splice_Rec_1740546 Human_miRNA_ID_2873861,Human_miRNA_ID_2969456,Human_miRNA_ID_2981824 RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_116812,RMVar_hsa_circ_115136,RMVar_hsa_circ_180016,RMVar_hsa_circ_96865,RMVar_hsa_circ_350367,RMVar_hsa_circ_180017,RMVar_hsa_circ_367393,RMVar_hsa_circ_300619,RMVar_hsa_circ_333951,RMVar_hsa_circ_180020,RMVar_hsa_circ_180022,RMVar_hsa_circ_46638,RMVar_hsa_circ_180021,RMVar_hsa_circ_348790,RMVar_hsa_circ_180037,RMVar_hsa_circ_4984,RMVar_hsa_circ_180023,RMVar_hsa_circ_180024,RMVar_hsa_circ_92597,RMVar_hsa_circ_84749,RMVar_hsa_circ_180028,RMVar_hsa_circ_343477,RMVar_hsa_circ_358496,RMVar_hsa_circ_332412,RMVar_hsa_circ_180031,RMVar_hsa_circ_7112,RMVar_hsa_circ_280918,RMVar_hsa_circ_308648,RMVar_hsa_circ_180030,RMVar_hsa_circ_296724,RMVar_hsa_circ_277941,RMVar_hsa_circ_120143,RMVar_hsa_circ_180033,RMVar_hsa_circ_180035,RMVar_hsa_circ_2684,RMVar_hsa_circ_180036,RMVar_hsa_circ_180034,RMVar_hsa_circ_274537,RMVar_hsa_circ_280144,RMVar_hsa_circ_180032,RMVar_hsa_circ_296155,RMVar_hsa_circ_277466,RMVar_hsa_circ_273813,RMVar_hsa_circ_180039,RMVar_hsa_circ_180041,RMVar_hsa_circ_180042,RMVar_hsa_circ_180040,RMVar_hsa_circ_180038 93248 RMVar_ID_93248 Human_SNP_ID_608763574 m1A Human chr16 - 74951479 74951479 74951479 AGACGGCAGTGGGGAAGTTGGCACAACCTTACAAGGCCACACTCGTGTCATCAGGTAGGCACCAG AGACGGCAGTGGGGAAGTTGGCACAACCTTACGAGGCCACACTCGTGTCATCAGGTAGGCACCAG T C WDR59 Ensembl:ENSG00000103091 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74951472..74956503 32194978 MeRIP-seq:(Medium) rs779613550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947967,Human_RBP_ID_22654496,Human_RBP_ID_26330272 Human_Splice_Rec_1740324,Human_Splice_Rec_1740325,Human_Splice_Rec_1740442,Human_Splice_Rec_1740443,Human_Splice_Rec_1740492,Human_Splice_Rec_1740493,Human_Splice_Rec_1740526,Human_Splice_Rec_1740527,Human_Splice_Rec_1740540,Human_Splice_Rec_1740541,Human_Splice_Rec_1740552,Human_Splice_Rec_1740553,Human_Splice_Rec_1740564,Human_Splice_Rec_1740565 Human_miRNA_ID_2600031,Human_miRNA_ID_2910609 RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_96865,RMVar_hsa_circ_367393,RMVar_hsa_circ_300619,RMVar_hsa_circ_333951,RMVar_hsa_circ_180020,RMVar_hsa_circ_180022,RMVar_hsa_circ_46638,RMVar_hsa_circ_180021,RMVar_hsa_circ_4984,RMVar_hsa_circ_180023,RMVar_hsa_circ_92597,RMVar_hsa_circ_358496,RMVar_hsa_circ_332412,RMVar_hsa_circ_180031,RMVar_hsa_circ_180030,RMVar_hsa_circ_296724,RMVar_hsa_circ_277941,RMVar_hsa_circ_180033,RMVar_hsa_circ_180034,RMVar_hsa_circ_274537,RMVar_hsa_circ_180032,RMVar_hsa_circ_277466,RMVar_hsa_circ_273813,RMVar_hsa_circ_180041,RMVar_hsa_circ_180042,RMVar_hsa_circ_180040,RMVar_hsa_circ_180047,RMVar_hsa_circ_180045,RMVar_hsa_circ_305790,RMVar_hsa_circ_370224,RMVar_hsa_circ_302741,RMVar_hsa_circ_180044,RMVar_hsa_circ_271582,RMVar_hsa_circ_313869,RMVar_hsa_circ_301208,RMVar_hsa_circ_111091,RMVar_hsa_circ_180048,RMVar_hsa_circ_180050,RMVar_hsa_circ_365513,RMVar_hsa_circ_180046,RMVar_hsa_circ_347046,RMVar_hsa_circ_180051,RMVar_hsa_circ_304019,RMVar_hsa_circ_358964 93249 RMVar_ID_93249 Human_SNP_ID_608774681 m1A Human chr16 - 74985017 74985017 74985017 CGTCCTGGGGCCGCGGCGGCCGGGCGGGGGAGATGGCGGCGCGATGGAGCAGCGAAAACGTGGTT CGTCCTGGGGCCGCGGCGGCCGGGCGGGGGAGGTGGCGGCGCGATGGAGCAGCGAAAACGTGGTT T C WDR59 Ensembl:ENSG00000103091 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:74984925..74985116 26863196 MeRIP-seq:(Medium) rs1447510500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_199311,Human_RBP_ID_233366,Human_RBP_ID_760847,Human_RBP_ID_818836,Human_RBP_ID_3947971,Human_RBP_ID_5113988,Human_RBP_ID_5419592,Human_RBP_ID_9325215,Human_RBP_ID_9419338,Human_RBP_ID_18418781,Human_RBP_ID_18986982,Human_RBP_ID_22426262,Human_RBP_ID_22532830,Human_RBP_ID_22712250,Human_RBP_ID_26330275,Human_RBP_ID_26769167,Human_RBP_ID_26949407 Human_Splice_Rec_1740319,Human_Splice_Rec_1740437,Human_Splice_Rec_1740567 RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_96865,RMVar_hsa_circ_180022,RMVar_hsa_circ_92597,RMVar_hsa_circ_180031,RMVar_hsa_circ_111091,RMVar_hsa_circ_180046 93250 RMVar_ID_93250 Human_SNP_ID_608774731 m1A Human chr16 + 74985085 74985085 74985085 CCCTCCCACCCCGCCGTCCCCAGTATCCCGGGACCGTGCGCCCCACACAGCCAGAGAATCAGCCC CCCTCCCACCCCGCCGTCCCCAGTATCCCGGGGCCGTGCGCCCCACACAGCCAGAGAATCAGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr16:74984951..74985125;chr16:74984984..74985123 26863196 MeRIP-seq:(Medium) rs1293482254 Functional Loss SNV dbSNP153 33..33 33 - - - 93251 RMVar_ID_93251 Human_SNP_ID_608774732 m1A Human chr16 + 74985085 74985085 74985085 CCCTCCCACCCCGCCGTCCCCAGTATCCCGGGACCGTGCGCCCCACACAGCCAGAGAATCAGCCC CCCTCCCACCCCGCCGTCCCCAGTATCCCGGGTCCGTGCGCCCCACACAGCCAGAGAATCAGCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr16:74984951..74985125;chr16:74984984..74985123 26863196 MeRIP-seq:(Medium) rs1293482254 Functional Loss SNV dbSNP153 33..33 33 - - - 93252 RMVar_ID_93252 Human_SNP_ID_608779690 m1A Human chr16 + 74999855 74999855 74999855 TCAGCTCGGTGGCAGGCATGGGCATGGACCCCAGCACGGCCGGGGGGGTGCCCTTTGGCCTCTAC TCAGCTCGGTGGCAGGCATGGGCATGGACCCCCGCACGGCCGGGGGGGTGCCCTTTGGCCTCTAC A C ZNRF1 Ensembl:ENSG00000186187 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74999805..74999889 26863196 MeRIP-seq:(Medium) rs756911197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815597 93253 RMVar_ID_93253 Human_SNP_ID_608779691 m1A Human chr16 + 74999855 74999855 74999855 TCAGCTCGGTGGCAGGCATGGGCATGGACCCCAGCACGGCCGGGGGGGTGCCCTTTGGCCTCTAC TCAGCTCGGTGGCAGGCATGGGCATGGACCCCGGCACGGCCGGGGGGGTGCCCTTTGGCCTCTAC A G ZNRF1 Ensembl:ENSG00000186187 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74999805..74999889 26863196 MeRIP-seq:(Medium) rs756911197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815597 93254 RMVar_ID_93254 Human_SNP_ID_422886072 m1A Human chr10 - 15103348 15103348 15103348 CTTCACAACCAGAGGTCTCGTCTTACGGAGAGATCCCCGCCCCGGTGCTTGAGGAGCTGCAGCCA CTTCACAACCAGAGGTCTCGTCTTACGGAGAGTTCCCCGCCCCGGTGCTTGAGGAGCTGCAGCCA T A NMT2 Ensembl:ENSG00000152465 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:15097575..15103489 32194978 MeRIP-seq:(Medium) rs554194985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374792,Human_RBP_ID_5949896,Human_RBP_ID_9360166 93255 RMVar_ID_93255 Human_SNP_ID_422898639 m1A Human chr10 + 15149283 15149281 15149284 TCACCATCACCATCGCCACTACCATTGCCATCACCACCATCACTGCCACCATCATCACCATCACC TCACCATCACCATCGCCACTACCATTGCCAT___CACCATCACTGCCACCATCATCACCATCACC TCAC T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:15149188..15149375 26863196 MeRIP-seq:(Medium) rs1334832054 Functional Loss DEL dbSNP153 32..34 33 - - - 93256 RMVar_ID_93256 Human_SNP_ID_422959244 m1A Human chr10 + 15371004 15371003 15371004 GGGCTCCCGCAGCGTCTTGGTCACCGCCTTCCAGACGTGGCAGCCCAGCAGGCACAGCAGCAGCG GGGCTCCCGCAGCGTCTTGGTCACCGCCTTCC_GACGTGGCAGCCCAGCAGGCACAGCAGCAGCG CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:15370977..15371089 26863196 MeRIP-seq:(Medium) rs1160348830 Functional Loss DEL dbSNP153 33..33 33 - - - 93257 RMVar_ID_93257 Human_SNP_ID_422989798 m1A Human chr10 - 15480473 15480473 15480473 GACTCCATCTCAAAAAAAAAAAAGAAAGAAAAAGTCTTCTGGATATAAGATTTTAAAGTTGACTT GACTCCATCTCAAAAAAAAAAAAGAAAGAAAAGGTCTTCTGGATATAAGATTTTAAAGTTGACTT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:15480399..15480481 26863410 MeRIP-seq:(Medium) rs550371298 Functional Loss SNV dbSNP153 33..33 33 - - - 93258 RMVar_ID_93258 Human_SNP_ID_423093066 m1A Human chr10 + 15860425 15860423 15860426 GGCGGCAAACGAATTGGAAGGTGAGGCAGGAAAGAAGAAGGGGCTGAGAGCCACTTGCAGAGACC GGCGGCAAACGAATTGGAAGGTGAGGCAGGA___AAGAAGGGGCTGAGAGCCACTTGCAGAGACC AAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:15860378..15860465 26863196 MeRIP-seq:(Medium) rs1439956176 Functional Loss DEL dbSNP153 32..34 33 - - - 93259 RMVar_ID_93259 Human_SNP_ID_423256953 m1A Human chr10 - 16437037 16437037 16437037 CTCTGACTCCAAGAAGCCTTACCTCGGGTACAACGCGCTGCCTTCTCCCTGGGAACTTCCGGCAG CTCTGACTCCAAGAAGCCTTACCTCGGGTACAGCGCGCTGCCTTCTCCCTGGGAACTTCCGGCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16436993..16437139 26863196 MeRIP-seq:(Medium) rs1037847465 Functional Loss SNV dbSNP153 33..33 33 - - - 93260 RMVar_ID_93260 Human_SNP_ID_423257107 m1A Human chr10 + 16437418 16437418 16437418 AGAGTGCATTTGGCGCGATCACAGCTCACTGCAGCCTCGACCTCCTGAGCTCAAGCGAACTTCCT AGAGTGCATTTGGCGCGATCACAGCTCACTGCGGCCTCGACCTCCTGAGCTCAAGCGAACTTCCT A G PTER Ensembl:ENSG00000165983 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:16437346..16437445 26863196 MeRIP-seq:(Medium) rs11558230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1115464 93261 RMVar_ID_93261 Human_SNP_ID_423265714 m1A Human chr10 - 16469138 16469119 16469138 CCCTAACCCTTTCCCAGTCCTGGCCAACTTCTACTCGGCCTTCAGCACTCTTCCTAACTAGAAGA CCCTAACCCTTTCCCAGTCCTGGCCAACTTCT___________________TCCTAACTAGAAGA AAGAGTGCTGAAGGCCGAGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16469136..16469237 26863196 MeRIP-seq:(Medium) rs1327161847 Functional Loss DEL dbSNP153 33..51 33 - - - 93262 RMVar_ID_93262 Human_SNP_ID_423308524 m1A Human chr10 - 16624350 16624350 16624350 AGTGATGGGCAGCCACAGAGGTGGAAGGAAAGAGGTTAGGGCAGTGGGACCAGAAAGGGAAGTAA AGTGATGGGCAGCCACAGAGGTGGAAGGAAAGTGGTTAGGGCAGTGGGACCAGAAAGGGAAGTAA T A RSU1 Ensembl:ENSG00000148484 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16624347..16624437 26863196 MeRIP-seq:(Medium) rs143332256 Functional Loss SNV dbSNP153 33..33 33 - - - 93263 RMVar_ID_93263 Human_SNP_ID_423356282 m1A Human chr10 + 16787290 16787290 16787290 TGGAATCTTGCGAGCCCTTTCAATTATCCAACACGTGTTCCACTATGTAGAGCAACCAATCTCCC TGGAATCTTGCGAGCCCTTTCAATTATCCAACCCGTGTTCCACTATGTAGAGCAACCAATCTCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16787287..16787494 26863196 MeRIP-seq:(Medium) rs1451616583 Functional Loss SNV dbSNP153 33..33 33 - - - 93264 RMVar_ID_93264 Human_SNP_ID_423356283 m1A Human chr10 + 16787290 16787290 16787290 TGGAATCTTGCGAGCCCTTTCAATTATCCAACACGTGTTCCACTATGTAGAGCAACCAATCTCCC TGGAATCTTGCGAGCCCTTTCAATTATCCAACGCGTGTTCCACTATGTAGAGCAACCAATCTCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16787287..16787494 26863196 MeRIP-seq:(Medium) rs1451616583 Functional Loss SNV dbSNP153 33..33 33 - - - 93265 RMVar_ID_93265 Human_SNP_ID_423365114 m1A Human chr10 - 16817373 16817373 16817373 GTGCCGGTGTTGCAGGGAGTGAGGGCAGCTGGAGTGCGTTCTGCCGAAGCTTGTGGTTGCACGCC GTGCCGGTGTTGCAGGGAGTGAGGGCAGCTGGGGTGCGTTCTGCCGAAGCTTGTGGTTGCACGCC T C RSU1 Ensembl:ENSG00000148484 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:16817278..16817428 26863196 MeRIP-seq:(Medium) rs147854078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1444857,Human_RBP_ID_4114842,Human_RBP_ID_22489694,Human_RBP_ID_23447579,Human_RBP_ID_26317006 Human_Splice_Rec_1115509,Human_Splice_Rec_1115525,Human_Splice_Rec_1115539,Human_Splice_Rec_1115553 93266 RMVar_ID_93266 Human_SNP_ID_423466400 m1A Human chr10 + 17201624 17201624 17201624 CGCCCACGCCGCTGTATAGCTCCAGCACCCGCAGGGGCTCCATCCCCGCGCCTCAGCCGCCGCAG CGCCCACGCCGCTGTATAGCTCCAGCACCCGCGGGGGCTCCATCCCCGCGCCTCAGCCGCCGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:17201558..17201650 26863196 MeRIP-seq:(Medium) rs1170371855 Functional Loss SNV dbSNP153 33..33 33 - - - 93267 RMVar_ID_93267 Human_SNP_ID_423471705 m1A Human chr10 - 17222303 17222303 17222303 ACGCGGAGATGATTTAAGGAATTGTGATGTTTAAGGGCTAGGGGATAAGAAAAATCGAGTGGGCT ACGCGGAGATGATTTAAGGAATTGTGATGTTTGAGGGCTAGGGGATAAGAAAAATCGAGTGGGCT T C VIM-AS1 Ensembl:ENSG00000229124 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:17222263..17222356 26863196 MeRIP-seq:(Medium) rs1302930226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5951545,Human_RBP_ID_11323270 93268 RMVar_ID_93268 Human_SNP_ID_423473715 m1A Human chr10 + 17229386 17229386 17229386 GTTCGCCTCTTCTCCGGGAGCCAGTCCGCGCCACCGCCGCCGCCCAGGCCATCGCCACCCTCCGC GTTCGCCTCTTCTCCGGGAGCCAGTCCGCGCCGCCGCCGCCGCCCAGGCCATCGCCACCCTCCGC A G VIM Ensembl:ENSG00000026025 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:17229276..17229978 26863196 MeRIP-seq:(Medium) rs1564372087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224965,Human_RBP_ID_1763819,Human_RBP_ID_4136178,Human_RBP_ID_5415003,Human_RBP_ID_5435286,Human_RBP_ID_8759903,Human_RBP_ID_17226384,Human_RBP_ID_17345580,Human_RBP_ID_17774117,Human_RBP_ID_22532201 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_266472,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142429,RMVar_hsa_circ_142426 93269 RMVar_ID_93269 Human_SNP_ID_423473749 m1A Human chr10 - 17229444 17229444 17229444 CGGGCCGCCGAACATCCTGCGGTAGGAGGACGAGGACACGGACCTGGTGGACATGGCTGCGGAGG CGGGCCGCCGAACATCCTGCGGTAGGAGGACGTGGACACGGACCTGGTGGACATGGCTGCGGAGG T A VIM-AS1 Ensembl:ENSG00000229124 lincRNA exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr10:17229343..17229492 26863410 MeRIP-seq:(Medium) rs1288770216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5548176,Human_RBP_ID_8245114 Human_Splice_Rec_1115879,Human_Splice_Rec_1115881 RMVar_hsa_circ_142430 93270 RMVar_ID_93270 Human_SNP_ID_423473938 m1A Human chr10 - 17229826 17229826 17229826 GGCGCGACTTGCCTTGGCCCTTGAGCTGCTCGAGCTCGGCCAGCAGGATCTTATTCTGCTGCTCC GGCGCGACTTGCCTTGGCCCTTGAGCTGCTCGTGCTCGGCCAGCAGGATCTTATTCTGCTGCTCC T A VIM-AS1 Ensembl:ENSG00000229124 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:17226891..17229839 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_8245302 RMVar_hsa_circ_96603,RMVar_hsa_circ_142431 93271 RMVar_ID_93271 Human_SNP_ID_423474074 m1A Human chr10 + 17230108 17230108 17230108 CCCTTGGGGATGTGGCCGGGGGGAGGCCTGCCAGGGAGACAGCGGAGAGCGGGGCTGTGGCTGTG CCCTTGGGGATGTGGCCGGGGGGAGGCCTGCCTGGGAGACAGCGGAGAGCGGGGCTGTGGCTGTG A T VIM Ensembl:ENSG00000026025 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:17230104..17230205 32194978 MeRIP-seq:(Medium) rs906123743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5339104,Human_RBP_ID_19047788,Human_RBP_ID_22639189 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_266472,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142429,RMVar_hsa_circ_142426 93272 RMVar_ID_93272 Human_SNP_ID_423475404 m1A Human chr10 + 17234771 17234771 17234771 GCCAGGCAAAGCAGGAGTCCACTGAGTACCGGAGACAGGTGCAGTCCCTCACCTGTGAAGTGGAT GCCAGGCAAAGCAGGAGTCCACTGAGTACCGGCGACAGGTGCAGTCCCTCACCTGTGAAGTGGAT A C VIM Ensembl:ENSG00000026025 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:17234661..17234866;chr10:17234675..17234774 26863196 MeRIP-seq:(Medium) rs762030566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26056,Human_RBP_ID_224970,Human_RBP_ID_375099,Human_RBP_ID_746971,Human_RBP_ID_1444900,Human_RBP_ID_1763833,Human_RBP_ID_3345382,Human_RBP_ID_4140746,Human_RBP_ID_5951590,Human_RBP_ID_8986298,Human_RBP_ID_17345584,Human_RBP_ID_17679797,Human_RBP_ID_22377302,Human_RBP_ID_22432362,Human_RBP_ID_23447726,Human_RBP_ID_26399649,Human_RBP_ID_26877815 Human_Splice_Rec_1115894,Human_Splice_Rec_1115895,Human_Splice_Rec_1115912,Human_Splice_Rec_1115913,Human_Splice_Rec_1115928,Human_Splice_Rec_1115929,Human_Splice_Rec_1115942,Human_Splice_Rec_1115943,Human_Splice_Rec_1115952,Human_Splice_Rec_1115960 Human_miRNA_ID_188571,Human_miRNA_ID_1472631,Human_miRNA_ID_2351666,Human_miRNA_ID_2750639,Human_miRNA_ID_3047212 RMVar_hsa_circ_10661,RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_112400,RMVar_hsa_circ_40197,RMVar_hsa_circ_82020,RMVar_hsa_circ_142434,RMVar_hsa_circ_142435,RMVar_hsa_circ_117850,RMVar_hsa_circ_37563,RMVar_hsa_circ_78427,RMVar_hsa_circ_95432,RMVar_hsa_circ_119637,RMVar_hsa_circ_142436,RMVar_hsa_circ_142437,RMVar_hsa_circ_103579,RMVar_hsa_circ_142438,RMVar_hsa_circ_142440,RMVar_hsa_circ_85982,RMVar_hsa_circ_142441,RMVar_hsa_circ_142439,RMVar_hsa_circ_142443,RMVar_hsa_circ_23969 93273 RMVar_ID_93273 Human_SNP_ID_423475563 m1A Human chr10 - 17235245 17235245 17235245 TCATATTCTGAATCTCATCCTGCAGGCGGCCAATAGTGTCTTGGTAGTTAGCAGCTTCAACGGCA TCATATTCTGAATCTCATCCTGCAGGCGGCCATTAGTGTCTTGGTAGTTAGCAGCTTCAACGGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:17235131..17235390 26863196 MeRIP-seq:(Medium) rs114322672 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93274 RMVar_ID_93274 Human_SNP_ID_423475564 m1A Human chr10 - 17235245 17235245 17235245 TCATATTCTGAATCTCATCCTGCAGGCGGCCAATAGTGTCTTGGTAGTTAGCAGCTTCAACGGCA TCATATTCTGAATCTCATCCTGCAGGCGGCCAGTAGTGTCTTGGTAGTTAGCAGCTTCAACGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:17235131..17235390 26863196 MeRIP-seq:(Medium) rs114322672 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93275 RMVar_ID_93275 Human_SNP_ID_423475857 m1A Human chr10 + 17236248 17236248 17236248 TGTTTCAGTAAAATGGTTACTTGGTTTTTCCAAGAAAAAACTCGTTTTTACTCATTTTTGGCCTG TGTTTCAGTAAAATGGTTACTTGGTTTTTCCAGGAAAAAACTCGTTTTTACTCATTTTTGGCCTG A G VIM Ensembl:ENSG00000026025 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:17236246..17237350 32194978 MeRIP-seq:(Medium) rs767913477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5951599,Human_RBP_ID_22639190 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_142425,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_112400,RMVar_hsa_circ_82020,RMVar_hsa_circ_142434,RMVar_hsa_circ_142435,RMVar_hsa_circ_117850,RMVar_hsa_circ_78427,RMVar_hsa_circ_119637,RMVar_hsa_circ_142436,RMVar_hsa_circ_142437,RMVar_hsa_circ_103579,RMVar_hsa_circ_142438,RMVar_hsa_circ_142439,RMVar_hsa_circ_75842,RMVar_hsa_circ_92840,RMVar_hsa_circ_142443,RMVar_hsa_circ_125809,RMVar_hsa_circ_142445,RMVar_hsa_circ_142446,RMVar_hsa_circ_142447 93276 RMVar_ID_93276 Human_SNP_ID_423576398 m1A Human chr10 + 17599386 17599386 17599386 TGATCTCTGTCACAGTCCACGCGACCAGAAAAAGCACCACACTCTCTTCATTCTGGATCTGCAGA TGATCTCTGTCACAGTCCACGCGACCAGAAAATGCACCACACTCTCTTCATTCTGGATCTGCAGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:17599209..17599408 32194978 MeRIP-seq:(Medium) rs781998397 Functional Loss SNV dbSNP153 33..33 33 - - - 93277 RMVar_ID_93277 Human_SNP_ID_423589730 m1A Human chr10 + 17644304 17644304 17644304 CTACGTCGAGCTCTGACTCCCGTGCTGTCGAGAGGGAGTCCCCGGGGACACCTCGGCACGCAGCG CTACGTCGAGCTCTGACTCCCGTGCTGTCGAGCGGGAGTCCCCGGGGACACCTCGGCACGCAGCG A C STAM Ensembl:ENSG00000136738 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:17644256..17644382 26863196 MeRIP-seq:(Medium) rs1554820501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136181,Human_RBP_ID_11324083,Human_RBP_ID_22029200,Human_RBP_ID_22886718 Human_Splice_Rec_1116065,Human_Splice_Rec_1116091,Human_Splice_Rec_1116103 RMVar_hsa_circ_124839,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_142469 93278 RMVar_ID_93278 Human_SNP_ID_423589731 m1A Human chr10 + 17644304 17644304 17644304 CTACGTCGAGCTCTGACTCCCGTGCTGTCGAGAGGGAGTCCCCGGGGACACCTCGGCACGCAGCG CTACGTCGAGCTCTGACTCCCGTGCTGTCGAGGGGGAGTCCCCGGGGACACCTCGGCACGCAGCG A G STAM Ensembl:ENSG00000136738 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:17644256..17644382 26863196 MeRIP-seq:(Medium) rs1554820501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136181,Human_RBP_ID_11324083,Human_RBP_ID_22029200,Human_RBP_ID_22886718 Human_Splice_Rec_1116065,Human_Splice_Rec_1116091,Human_Splice_Rec_1116103 RMVar_hsa_circ_124839,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_142469 93279 RMVar_ID_93279 Human_SNP_ID_423841274 m1A Human chr10 - 18563980 18563975 18563980 ATGGAATGCAGTGGAATGGAGAATGGAATGGAATGGAGTGGAGAATAGAAAGGAATCGAGAATGG ATGGAATGCAGTGGAATGGAGAATGGAATGGA_____GTGGAGAATAGAAAGGAATCGAGAATGG CTCCAT C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18563929..18564012 26863196 MeRIP-seq:(Medium) rs796760640 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_191786,Human_RBP_ID_5643227,Human_RBP_ID_24550719 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93280 RMVar_ID_93280 Human_SNP_ID_423841276 m1A Human chr10 - 18563980 18563980 18563980 ATGGAATGCAGTGGAATGGAGAATGGAATGGAATGGAGTGGAGAATAGAAAGGAATCGAGAATGG ATGGAATGCAGTGGAATGGAGAATGGAATGGAGTGGAGTGGAGAATAGAAAGGAATCGAGAATGG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18563929..18564012 26863196 MeRIP-seq:(Medium) rs534303978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191786,Human_RBP_ID_5643227,Human_RBP_ID_24550719 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93281 RMVar_ID_93281 Human_SNP_ID_423841474 m1A Human chr10 - 18564547 18564531 18564548 GAAGTGGAGAATGGAATAGAGAATGGAATGGAATGGACAATGGAATGGGGAATGGAATGGAGTGG GAAGTGGAGAATGGAATAGAGAATGGAATGG_________________GGAATGGAATGGAGTGG CCCATTCCATTGTCCATT C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:18564371..18564805 26863196 MeRIP-seq:(Medium) rs574207918 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_191790,Human_RBP_ID_5234749 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93282 RMVar_ID_93282 Human_SNP_ID_423841476 m1A Human chr10 - 18564540 18564540 18564540 AGAATGGAATAGAGAATGGAATGGAATGGACAATGGAATGGGGAATGGAATGGAGTGGAGAATGG AGAATGGAATAGAGAATGGAATGGAATGGACAGTGGAATGGGGAATGGAATGGAGTGGAGAATGG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:18564513..18564642 26863196 MeRIP-seq:(Medium) rs543258966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191790,Human_RBP_ID_5234570,Human_RBP_ID_5642895 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93283 RMVar_ID_93283 Human_SNP_ID_423841479 m1A Human chr10 - 18564547 18564542 18564547 GAAGTGGAGAATGGAATAGAGAATGGAATGGAATGGACAATGGAATGGGGAATGGAATGGAGTGG GAAGTGGAGAATGGAATAGAGAATGGAATGGA_____CAATGGAATGGGGAATGGAATGGAGTGG GTCCAT G NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:18564371..18564805 26863196 MeRIP-seq:(Medium) rs1397019240 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_191790,Human_RBP_ID_5234749 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93284 RMVar_ID_93284 Human_SNP_ID_423841750 m1A Human chr10 - 18565376 18565376 18565376 ATGGAATGGAGAATGGTATGGAATGGAAGGGAATGAAATGGAGAGTGGAAGGGAATAGAATGGAG ATGGAATGGAGAATGGTATGGAATGGAAGGGAGTGAAATGGAGAGTGGAAGGGAATAGAATGGAG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18565357..18565484 26863196 MeRIP-seq:(Medium) rs1253640222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5642900,Human_RBP_ID_9443882 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93285 RMVar_ID_93285 Human_SNP_ID_423842220 m1A Human chr10 - 18566555 18566555 18566555 AGAGTAGAATGCAATAGAATGGAATGGAATGGAGAATGGAATGGATTGGACAGGAATGTAGAATG AGAGTAGAATGCAATAGAATGGAATGGAATGGGGAATGGAATGGATTGGACAGGAATGTAGAATG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18566509..18566620 26863196 MeRIP-seq:(Medium) rs1159949499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93286 RMVar_ID_93286 Human_SNP_ID_423842221 m1A Human chr10 - 18566555 18566555 18566555 AGAGTAGAATGCAATAGAATGGAATGGAATGGAGAATGGAATGGATTGGACAGGAATGTAGAATG AGAGTAGAATGCAATAGAATGGAATGGAATGGCGAATGGAATGGATTGGACAGGAATGTAGAATG T G NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18566509..18566620 26863196 MeRIP-seq:(Medium) rs1159949499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93287 RMVar_ID_93287 Human_SNP_ID_423842363 m1A Human chr10 + 18566946 18566946 18566946 TCCATTCCACTCCATTCTCCATTCCAGCCTCCATTATATTTCATTCTATTCCATTCTCCATTCCA TCCATTCCACTCCATTCTCCATTCCAGCCTCCGTTATATTTCATTCTATTCCATTCTCCATTCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18566841..18566995 26863196 MeRIP-seq:(Medium) rs1351441667 Functional Loss SNV dbSNP153 33..33 33 - - - 93288 RMVar_ID_93288 Human_SNP_ID_423842483 m1A Human chr10 + 18567348 18567348 18567348 ATTCACCAATGCATTCCATTCCATTCCATTCTATTCTCCATTCCATTCCATATTCCATTTTCCAT ATTCACCAATGCATTCCATTCCATTCCATTCTGTTCTCCATTCCATTCCATATTCCATTTTCCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18567299..18567384 26863196 MeRIP-seq:(Medium) rs1272560083 Functional Loss SNV dbSNP153 33..33 33 - - - 93289 RMVar_ID_93289 Human_SNP_ID_423842552 m1A Human chr10 - 18567520 18567520 18567520 AAGAGAATGGAATGGAGAACGGAATGGGATGCAGTGGTGAATAGAATGGAATGGAGAATGGAATG AAGAGAATGGAATGGAGAACGGAATGGGATGCGGTGGTGAATAGAATGGAATGGAGAATGGAATG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18567518..18567606 26863196 MeRIP-seq:(Medium) rs986956657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5162645,Human_RBP_ID_5643235,Human_RBP_ID_9443863 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93290 RMVar_ID_93290 Human_SNP_ID_423842772 m1A Human chr10 - 18568081 18568081 18568081 GGAATGGAGCATGGAGTGCAATGAAATAGAGAATGGAATGGAATGGAACGGAAAATGGAGAATGG GGAATGGAGCATGGAGTGCAATGAAATAGAGAGTGGAATGGAATGGAACGGAAAATGGAGAATGG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18568031..18568125 26863196 MeRIP-seq:(Medium) rs1392340850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1756,Human_RBP_ID_23448231 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93291 RMVar_ID_93291 Human_SNP_ID_423843095 m1A Human chr10 - 18568937 18568937 18568937 AATAGAATGGAGAATGGATTGGAATGGAATGGAGAACCAAATGGAGAATGGAATGGAATGGAGAG AATAGAATGGAGAATGGATTGGAATGGAATGGGGAACCAAATGGAGAATGGAATGGAATGGAGAG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18568918..18568983 26863196 MeRIP-seq:(Medium) rs1419452317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93292 RMVar_ID_93292 Human_SNP_ID_423843146 m1A Human chr10 + 18569113 18569113 18569113 TCCATTCAATTCCACATTCCATTCCATTCTCCATCCGTTACATTCTCCATTCCATTCCCCATTCC TCCATTCAATTCCACATTCCATTCCATTCTCCGTCCGTTACATTCTCCATTCCATTCCCCATTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18569094..18569310 26863196 MeRIP-seq:(Medium) rs1171313533 Functional Loss SNV dbSNP153 33..33 33 - - - 93293 RMVar_ID_93293 Human_SNP_ID_423843698 m1A Human chr10 - 18570636 18570636 18570636 AGAATGGAATGGAATGGATGATGGTATGGAGAATGGAATGGAATGGAGAATGGAATGGAATGGAC AGAATGGAATGGAATGGATGATGGTATGGAGAGTGGAATGGAATGGAGAATGGAATGGAATGGAC T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:18570365..18570790 26863196 MeRIP-seq:(Medium) rs1185362333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93294 RMVar_ID_93294 Human_SNP_ID_423844541 m1A Human chr10 - 18573062 18573062 18573062 ATGGAATGGAGTGGAACGGAGAATGGAATGGAATGGAGAAGAGAATGGAGAATGGAATGGAATGA ATGGAATGGAGTGGAACGGAGAATGGAATGGATTGGAGAAGAGAATGGAGAATGGAATGGAATGA T A NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18572808..18573167 26863196 MeRIP-seq:(Medium) rs117700259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191798,Human_RBP_ID_5642931,Human_RBP_ID_23481120 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93295 RMVar_ID_93295 Human_SNP_ID_423844542 m1A Human chr10 - 18573062 18573062 18573062 ATGGAATGGAGTGGAACGGAGAATGGAATGGAATGGAGAAGAGAATGGAGAATGGAATGGAATGA ATGGAATGGAGTGGAACGGAGAATGGAATGGAGTGGAGAAGAGAATGGAGAATGGAATGGAATGA T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:18572808..18573167 26863196 MeRIP-seq:(Medium) rs117700259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191798,Human_RBP_ID_5642931,Human_RBP_ID_23481120 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93296 RMVar_ID_93296 Human_SNP_ID_423844701 m1A Human chr10 - 18573416 18573416 18573416 GGAATGGAGAATGGAATGGAAAGGAAAATGGAACCGATGGAATGGAAGGGAGAATGGAATGGAAT GGAATGGAGAATGGAATGGAAAGGAAAATGGAGCCGATGGAATGGAAGGGAGAATGGAATGGAAT T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18573365..18573481 26863196 MeRIP-seq:(Medium) rs548019574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191801 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 93297 RMVar_ID_93297 Human_SNP_ID_423848838 m1A Human chr10 - 18586873 18586873 18586873 GATTGTAAATGCACCAATCAGCACTGTGTAAAATGGACCAATCAGCGCTCTGTAAAATGGACCAA GATTGTAAATGCACCAATCAGCACTGTGTAAATTGGACCAATCAGCGCTCTGTAAAATGGACCAA T A NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18586868..18586962 26863196 MeRIP-seq:(Medium) rs149775197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30562,RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_304992,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695,RMVar_hsa_circ_353618,RMVar_hsa_circ_367694,RMVar_hsa_circ_369431,RMVar_hsa_circ_313309,RMVar_hsa_circ_267252,RMVar_hsa_circ_291385,RMVar_hsa_circ_142501,RMVar_hsa_circ_142503,RMVar_hsa_circ_142504,RMVar_hsa_circ_142505,RMVar_hsa_circ_142502 93298 RMVar_ID_93298 Human_SNP_ID_423871405 m1A Human chr10 + 18659446 18659444 18659447 GGGTCGGCGTTGGGCTCAGTGGGCTCGAAACAAAGGGCTGTCCGGTGGGGATTCGTCGCGGCGCC GGGTCGGCGTTGGGCTCAGTGGGCTCGAAAC___GGGCTGTCCGGTGGGGATTCGTCGCGGCGCC CAAA C ARL5B Ensembl:ENSG00000165997 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:18659342..18659542 26863196 MeRIP-seq:(Medium) rs1291196989 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5459173,Human_RBP_ID_22152486 RMVar_hsa_circ_83841,RMVar_hsa_circ_142515 93299 RMVar_ID_93299 Human_SNP_ID_423871406 m1A Human chr10 + 18659446 18659446 18659446 GGGTCGGCGTTGGGCTCAGTGGGCTCGAAACAAAGGGCTGTCCGGTGGGGATTCGTCGCGGCGCC GGGTCGGCGTTGGGCTCAGTGGGCTCGAAACATAGGGCTGTCCGGTGGGGATTCGTCGCGGCGCC A T ARL5B Ensembl:ENSG00000165997 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:18659342..18659542 26863196 MeRIP-seq:(Medium) rs1433814237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5459173,Human_RBP_ID_22152486 RMVar_hsa_circ_83841,RMVar_hsa_circ_142515 93300 RMVar_ID_93300 Human_SNP_ID_423871407 m1A Human chr10 - 18659452 18659451 18659452 TCAGAAGGCGCCGCGACGAATCCCCACCGGACAGCCCTTTGTTTCGAGCCCACTGAGCCCAACGC TCAGAAGGCGCCGCGACGAATCCCCACCGGAC_GCCCTTTGTTTCGAGCCCACTGAGCCCAACGC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:18659354..18659655 26863196 MeRIP-seq:(Medium) rs546240282 Functional Loss DEL dbSNP153 33..33 33 - - - 93301 RMVar_ID_93301 Human_SNP_ID_423871409 m1A Human chr10 - 18659452 18659452 18659452 TCAGAAGGCGCCGCGACGAATCCCCACCGGACAGCCCTTTGTTTCGAGCCCACTGAGCCCAACGC TCAGAAGGCGCCGCGACGAATCCCCACCGGACTGCCCTTTGTTTCGAGCCCACTGAGCCCAACGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:18659354..18659655 26863196 MeRIP-seq:(Medium) rs538289611 Functional Loss SNV dbSNP153 33..33 33 - - - 93302 RMVar_ID_93302 Human_SNP_ID_423871448 m1A Human chr10 - 18659554 18659554 18659554 CCGGGTCCCCCACCGCGGCGCGGGCTGCGCGGAGCCGAGGAGAACCCGCCTGAGATCGCGCAGCG CCGGGTCCCCCACCGCGGCGCGGGCTGCGCGGGGCCGAGGAGAACCCGCCTGAGATCGCGCAGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:18659504..18668540 32194978 MeRIP-seq:(Medium) rs1312545919 Functional Loss SNV dbSNP153 33..33 33 - - - 93303 RMVar_ID_93303 Human_SNP_ID_423877285 m1A Human chr10 + 18678861 18678861 18678861 TGAGCCTTAATTTGGCCGTTTCTCAATTGTCTAGTTGACCTTAGACAATTAGTGTCCATGGCTTT TGAGCCTTAATTTGGCCGTTTCTCAATTGTCTGGTTGACCTTAGACAATTAGTGTCCATGGCTTT A G ARL5B Ensembl:ENSG00000165997 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:18678812..18678914 32194978 MeRIP-seq:(Medium) rs1217534814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_375370,Human_RBP_ID_8760017,Human_RBP_ID_11327920 93304 RMVar_ID_93304 Human_SNP_ID_424182272 m1A Human chr10 - 19746813 19746813 19746813 AGAGGTGATGTTTTTGGTAAACAGGCGGGGTAAGATTGGCTGAATTCCTTTTACTTTTTGTAATC AGAGGTGATGTTTTTGGTAAACAGGCGGGGTAGGATTGGCTGAATTCCTTTTACTTTTTGTAATC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:19746778..19746929 26863196 MeRIP-seq:(Medium) rs975360528 Functional Loss SNV dbSNP153 33..33 33 - - - 93305 RMVar_ID_93305 Human_SNP_ID_424573357 m1A Human chr10 - 21173868 21173868 21173868 GGGGGATGTCACAGCGGCTCCTGGGAGCCAGCAGCCGCCGCCGCCGCCGCCCCCGGGAACCGCGA GGGGGATGTCACAGCGGCTCCTGGGAGCCAGCCGCCGCCGCCGCCGCCGCCCCCGGGAACCGCGA T G NEBL Ensembl:ENSG00000078114 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr10:21173844..21173970;chr10:21173828..21173981 26863196 MeRIP-seq:(Medium) rs552261723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4140835 93306 RMVar_ID_93306 Human_SNP_ID_424573412 m1A Human chr10 - 21174017 21174017 21174017 GCGCCTGCGAGCCCGAGAGCGCGGCCGGCCCCAGGCGCCAGGCCCCGTCGCCCTCCCCGTGCACT GCGCCTGCGAGCCCGAGAGCGCGGCCGGCCCCCGGCGCCAGGCCCCGTCGCCCTCCCCGTGCACT T G NEBL Ensembl:ENSG00000078114 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr10:21173847..21174324;chr10:21173837..21174137 26863196,26863410 MeRIP-seq:(Medium) rs983149883 Functional Loss SNV dbSNP153 33..33 33 - - - 93307 RMVar_ID_93307 Human_SNP_ID_424658875 m1A Human chr10 - 21497179 21497179 21497179 TGGAGCTGACGGCGCCGGGCTGCGTCCTCTTCACCTGGGGGTGGGGGGTGGGGGCACGTACTTTG TGGAGCTGACGGCGCCGGGCTGCGTCCTCTTCGCCTGGGGGTGGGGGGTGGGGGCACGTACTTTG T C MIR1915HG Ensembl:ENSG00000204682 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:21497129..21497240 26863196 MeRIP-seq:(Medium) rs1408733194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4115356,Human_RBP_ID_5488020 93308 RMVar_ID_93308 Human_SNP_ID_424663958 m1A Human chr10 - 21516813 21516813 21516813 TCATCTGGTCAACGGCTTCTGCCCGCCTCCGCACCACCACCACCACCACCACCATCACCACCACC TCATCTGGTCAACGGCTTCTGCCCGCCTCCGCCCCACCACCACCACCACCACCATCACCACCACC T G SKIDA1 Ensembl:ENSG00000180592 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21516778..21516862 26863196 MeRIP-seq:(Medium) rs1194807916 Functional Loss SNV dbSNP153 33..33 33 - - - 93309 RMVar_ID_93309 Human_SNP_ID_424664056 m1A Human chr10 - 21516918 21516916 21516919 CCTGCTGCTGTTGCCCAGGTCCTACAAAGCCAAGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGG CCTGCTGCTGTTGCCCAGGTCCTACAAAGCC___GCGGCGGCGGCGGCGGCGGCGGCGGCAGCGG CCTT C SKIDA1 Ensembl:ENSG00000180592 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21516773..21516950 26863196 MeRIP-seq:(Medium) rs1193220273 Functional Loss DEL dbSNP153 32..34 33 - - - 93310 RMVar_ID_93310 Human_SNP_ID_424664146 m1A Human chr10 + 21517124 21517094 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCG______________________________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCGGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1339832341 Functional Loss DEL dbSNP153 4..33 33 - - - 93311 RMVar_ID_93311 Human_SNP_ID_424664149 m1A Human chr10 + 21517124 21517097 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCG___________________________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1193412048 Functional Loss DEL dbSNP153 7..33 33 - - - 93312 RMVar_ID_93312 Human_SNP_ID_424664151 m1A Human chr10 + 21517124 21517100 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCG________________________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs767464686 Functional Loss DEL dbSNP153 10..33 33 - - - 93313 RMVar_ID_93313 Human_SNP_ID_424664157 m1A Human chr10 + 21517124 21517103 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCG_____________________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1251465132 Functional Loss DEL dbSNP153 13..33 33 - - - 93314 RMVar_ID_93314 Human_SNP_ID_424664160 m1A Human chr10 + 21517124 21517106 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCG__________________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs993815009 Functional Loss DEL dbSNP153 16..33 33 - - - 93315 RMVar_ID_93315 Human_SNP_ID_424664163 m1A Human chr10 + 21517124 21517109 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCGGCG_______________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1455988251 Functional Loss DEL dbSNP153 19..33 33 - - - 93316 RMVar_ID_93316 Human_SNP_ID_424664165 m1A Human chr10 + 21517124 21517112 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCGGCGGCG____________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1317570874 Functional Loss DEL dbSNP153 22..33 33 - - - 93317 RMVar_ID_93317 Human_SNP_ID_424664168 m1A Human chr10 + 21517124 21517115 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCGGCGGCGGCG_________GCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GGCGGCAGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs1289380619 Functional Loss DEL dbSNP153 25..33 33 - - - 93318 RMVar_ID_93318 Human_SNP_ID_424664181 m1A Human chr10 + 21517124 21517124 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs868442911 Functional Loss SNV dbSNP153 33..33 33 - - - 93319 RMVar_ID_93319 Human_SNP_ID_424665562 m1A Human chr10 + 21522266 21522266 21522266 ATACATACATAATTTAAATGAGGATCACAGCCACCCCCCCCCCCCCCCCCCCCCCCCCGCCACCA ATACATACATAATTTAAATGAGGATCACAGCCCCCCCCCCCCCCCCCCCCCCCCCCCCGCCACCA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:21522251..21522300 26863196 MeRIP-seq:(Medium) rs1420897721 Functional Loss SNV dbSNP153 33..33 33 - - - 93320 RMVar_ID_93320 Human_SNP_ID_424669200 m1A Human chr10 - 21534840 21534817 21534841 CCCAGGTGGGGGCGGCGGTGACCGTTGGGCGCAGGCCGGCGCGCCCCGGCGGGCGGTTGGGTGTT CCCAGGTGGGGGCGGCGGTGACCGTTGGGCG________________________GTTGGGTGTT CCGCCCGCCGGGGCGCGCCGGCCTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21534824..21535015 26863196 MeRIP-seq:(Medium) rs1299324424 Functional Loss DEL dbSNP153 32..55 33 - - - 93321 RMVar_ID_93321 Human_SNP_ID_424669222 m1A Human chr10 - 21534840 21534840 21534840 CCCAGGTGGGGGCGGCGGTGACCGTTGGGCGCAGGCCGGCGCGCCCCGGCGGGCGGTTGGGTGTT CCCAGGTGGGGGCGGCGGTGACCGTTGGGCGCGGGCCGGCGCGCCCCGGCGGGCGGTTGGGTGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21534824..21535015 26863196 MeRIP-seq:(Medium) rs1406934751 Functional Loss SNV dbSNP153 33..33 33 - - - 93322 RMVar_ID_93322 Human_SNP_ID_424669264 m1A Human chr10 + 21534914 21534914 21534914 CCGGCGCCCCCGCCCCGTGCCGCGGCCGCGGGAGGGACGCGGAGGGTCCGCGGCGGGGCGCGGGG CCGGCGCCCCCGCCCCGTGCCGCGGCCGCGGGGGGGACGCGGAGGGTCCGCGGCGGGGCGCGGGG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21534908..21535020 26863196 MeRIP-seq:(Medium) rs1380926843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3363844,Human_RBP_ID_8059131 RMVar_hsa_circ_41652,RMVar_hsa_circ_365259,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578 93323 RMVar_ID_93323 Human_SNP_ID_424695255 m1A Human chr10 + 21630172 21630172 21630172 AGATATTGCTAGGCAGATTGGGTATACAAATAAGGAGGCCAAGTGCGTTATTTTCAAAAGTGTTT AGATATTGCTAGGCAGATTGGGTATACAAATAGGGAGGCCAAGTGCGTTATTTTCAAAAGTGTTT A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21630162..21630395 26863196 MeRIP-seq:(Medium) rs1004572039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5954284 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_361775,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_283296,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_288611,RMVar_hsa_circ_58461,RMVar_hsa_circ_9911,RMVar_hsa_circ_142584,RMVar_hsa_circ_337991,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_278812,RMVar_hsa_circ_377825,RMVar_hsa_circ_142588,RMVar_hsa_circ_61898,RMVar_hsa_circ_313538,RMVar_hsa_circ_368910,RMVar_hsa_circ_65965 93324 RMVar_ID_93324 Human_SNP_ID_424701328 m1A Human chr10 + 21654170 21654170 21654170 TAAAGTACTGATTGAGGCAAAAGCCTGATTGGAGTGCTTTATAGAGAGAATGGGGGAGAAAAGTC TAAAGTACTGATTGAGGCAAAAGCCTGATTGGGGTGCTTTATAGAGAGAATGGGGGAGAAAAGTC A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21654164..21654408 26863196 MeRIP-seq:(Medium) rs1237457492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23449532 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_361775,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_9911,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_377825,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_368910,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_298322,RMVar_hsa_circ_25936,RMVar_hsa_circ_142590,RMVar_hsa_circ_142591 93325 RMVar_ID_93325 Human_SNP_ID_424714996 m1A Human chr10 + 21705507 21705507 21705507 TGATCCCTAAGTCACCAGCAGAATGTTCAGGTAGCCGGGGCAGCATTGGTCACACCGTTGCCCTG TGATCCCTAAGTCACCAGCAGAATGTTCAGGTTGCCGGGGCAGCATTGGTCACACCGTTGCCCTG A T MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21705141..21705571 26863196 MeRIP-seq:(Medium) rs897105815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142597,RMVar_hsa_circ_268026,RMVar_hsa_circ_286617,RMVar_hsa_circ_377400,RMVar_hsa_circ_142595,RMVar_hsa_circ_276739,RMVar_hsa_circ_74327,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_84528,RMVar_hsa_circ_359005,RMVar_hsa_circ_289028,RMVar_hsa_circ_53576,RMVar_hsa_circ_19368,RMVar_hsa_circ_28893,RMVar_hsa_circ_142601,RMVar_hsa_circ_142602,RMVar_hsa_circ_332502,RMVar_hsa_circ_309660,RMVar_hsa_circ_303644,RMVar_hsa_circ_142603,RMVar_hsa_circ_45753,RMVar_hsa_circ_7458 93326 RMVar_ID_93326 Human_SNP_ID_424715524 m1A Human chr10 + 21707520 21707520 21707520 GCCAAGTTTAGATGATTCTAATTTCTAGATGCACTGCAAGTCCTTGTCCGTGTTCAGTACTACTA GCCAAGTTTAGATGATTCTAATTTCTAGATGCGCTGCAAGTCCTTGTCCGTGTTCAGTACTACTA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:21707470..21707543 26863196 MeRIP-seq:(Medium) rs999508479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1260304,Human_RBP_ID_11333155 RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142597,RMVar_hsa_circ_268026,RMVar_hsa_circ_286617,RMVar_hsa_circ_377400,RMVar_hsa_circ_142595,RMVar_hsa_circ_276739,RMVar_hsa_circ_74327,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_84528,RMVar_hsa_circ_359005,RMVar_hsa_circ_289028,RMVar_hsa_circ_53576,RMVar_hsa_circ_19368,RMVar_hsa_circ_28893,RMVar_hsa_circ_142601,RMVar_hsa_circ_142602,RMVar_hsa_circ_332502,RMVar_hsa_circ_309660,RMVar_hsa_circ_303644,RMVar_hsa_circ_142603,RMVar_hsa_circ_45753,RMVar_hsa_circ_7458 93327 RMVar_ID_93327 Human_SNP_ID_424723070 m1A Human chr10 + 21735698 21735698 21735698 CGATGTGAGAGTTCAGGGAGTGTGCCTTTGTGACTTGAGGGAACGCAGAGAGAAAGCACGTTGGA CGATGTGAGAGTTCAGGGAGTGTGCCTTTGTGGCTTGAGGGAACGCAGAGAGAAAGCACGTTGGA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:21735648..21735734 26863196 MeRIP-seq:(Medium) rs779813345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11333537 RMVar_hsa_circ_63935,RMVar_hsa_circ_142612 93328 RMVar_ID_93328 Human_SNP_ID_424723427 m1A Human chr10 + 21736951 21736951 21736951 AAGGAGAATAAGCCAGTAAAGAAAGGCTATTGAGAAACTGTGGCCAGTGAGCCAAGAGAAGGACA AAGGAGAATAAGCCAGTAAAGAAAGGCTATTGGGAAACTGTGGCCAGTGAGCCAAGAGAAGGACA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21736925..21737063 26863196 MeRIP-seq:(Medium) rs904578998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11333586 RMVar_hsa_circ_63935 93329 RMVar_ID_93329 Human_SNP_ID_424850316 m1A Human chr10 - 22229524 22229524 22229524 GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGAGCCCACCCAGGGACGCGCTCTCCTTTTATGAG GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGGGCCCACCCAGGGACGCGCTCTCCTTTTATGAG T C piR-37182,piR-59260,piR-37183,tRNA-Asn-GTT-2-1,lnc-EBLN1-1,piR-59259,lnc-EBLN1-1:2,TRN,piR-36706,piR-36705 RNACentral:URS00003B4A72,RNACentral:URS00005F0138,RNACentral:URS00003905DB,RNACentral:URS000059D2BF,RNACentral:URS00008BC03A,RNACentral:URS00000E6438,RNACentral:URS0000D585BE,RNACentral:URS00001246A7,RNACentral:URS000020012B,RNACentral:URS00004F59A9 piRNA,piRNA,piRNA,tRNA,lincRNA,piRNA,lincRNA,tRNA,piRNA,piRNA intron,intron,intron,exon,intron,intron,intron,exon,intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1396888286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_375621,Human_RBP_ID_1445185,Human_RBP_ID_5273546,Human_RBP_ID_5548746,Human_RBP_ID_5955537,Human_RBP_ID_8244569,Human_RBP_ID_8331936,Human_RBP_ID_17073554,Human_RBP_ID_17581319,Human_RBP_ID_18205570,Human_RBP_ID_18431596,Human_RBP_ID_19502440,Human_RBP_ID_22788034,Human_RBP_ID_23123540,Human_RBP_ID_26884732 93330 RMVar_ID_93330 Human_SNP_ID_424850317 m1A Human chr10 - 22229524 22229524 22229524 GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGAGCCCACCCAGGGACGCGCTCTCCTTTTATGAG GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGCGCCCACCCAGGGACGCGCTCTCCTTTTATGAG T G piR-37182,piR-59260,piR-37183,tRNA-Asn-GTT-2-1,lnc-EBLN1-1,piR-59259,lnc-EBLN1-1:2,TRN,piR-36706,piR-36705 RNACentral:URS00003B4A72,RNACentral:URS00005F0138,RNACentral:URS00003905DB,RNACentral:URS000059D2BF,RNACentral:URS00008BC03A,RNACentral:URS00000E6438,RNACentral:URS0000D585BE,RNACentral:URS00001246A7,RNACentral:URS000020012B,RNACentral:URS00004F59A9 piRNA,piRNA,piRNA,tRNA,lincRNA,piRNA,lincRNA,tRNA,piRNA,piRNA intron,intron,intron,exon,intron,intron,intron,exon,intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1396888286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_375621,Human_RBP_ID_1445185,Human_RBP_ID_5273546,Human_RBP_ID_5548746,Human_RBP_ID_5955537,Human_RBP_ID_8244569,Human_RBP_ID_8331936,Human_RBP_ID_17073554,Human_RBP_ID_17581319,Human_RBP_ID_18205570,Human_RBP_ID_18431596,Human_RBP_ID_19502440,Human_RBP_ID_22788034,Human_RBP_ID_23123540,Human_RBP_ID_26884732 93331 RMVar_ID_93331 Human_SNP_ID_424871541 m1A Human chr10 - 22316465 22316465 22316465 AGCGTGAAGGCGTTGGAGTCGAAGGAGCGGGGATCCGCCAGCATCTGGAAGCCTTTCTGCACAGA AGCGTGAAGGCGTTGGAGTCGAAGGAGCGGGGCTCCGCCAGCATCTGGAAGCCTTTCTGCACAGA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:22316418..22316519 26863196 MeRIP-seq:(Medium) rs1564345406 Functional Loss SNV dbSNP153 33..33 33 - - - 93332 RMVar_ID_93332 Human_SNP_ID_424871554 m1A Human chr10 + 22316485 22316485 22316485 GATGCTGGCGGATCCCCGCTCCTTCGACTCCAACGCCTTCACGCTTCTCCTCCGGGCGGCATTCC GATGCTGGCGGATCCCCGCTCCTTCGACTCCAGCGCCTTCACGCTTCTCCTCCGGGCGGCATTCC A G COMMD3,COMMD3-BMI1 Ensembl:ENSG00000148444,Ensembl:ENSG00000269897 Protein coding,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:22316436..22316612 26863196 MeRIP-seq:(Medium) rs373854912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136186 Human_Splice_Rec_1117867,Human_Splice_Rec_1117875,Human_Splice_Rec_1117889,Human_Splice_Rec_1117895,Human_Splice_Rec_1117903,Human_Splice_Rec_1117905,Human_Splice_Rec_1117915,Human_Splice_Rec_1117925,Human_Splice_Rec_1117933,Human_Splice_Rec_1117945,Human_Splice_Rec_1117953,Human_Splice_Rec_1117997,Human_Splice_Rec_1118005,Human_Splice_Rec_1118031,Human_Splice_Rec_1118035,Human_Splice_Rec_1118049 Human_miRNA_ID_2369978 RMVar_hsa_circ_127457,RMVar_hsa_circ_142627 93333 RMVar_ID_93333 Human_SNP_ID_424871575 m1A Human chr10 - 22316524 22316523 22316524 CTAACACGGCCTCGTCCGCCTGGGCGTCCAGCAGACTCTGGAATGCCGCCCGGAGGAGAAGCGTG CTAACACGGCCTCGTCCGCCTGGGCGTCCAGC_GACTCTGGAATGCCGCCCGGAGGAGAAGCGTG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:22316476..22316525 26863196 MeRIP-seq:(Medium) rs1345604308 Functional Loss DEL dbSNP153 33..33 33 - - - 93334 RMVar_ID_93334 Human_SNP_ID_424871963 m1A Human chr10 + 22317982 22317981 22317982 ACATACTAGAGGCAGGAAAGCACCGAGCTGACAAGTCAACTCTAAGGTACAGGATTTATTTAAAT ACATACTAGAGGCAGGAAAGCACCGAGCTGAC_AGTCAACTCTAAGGTACAGGATTTATTTAAAT CA C COMMD3,COMMD3-BMI1 Ensembl:ENSG00000148444,Ensembl:ENSG00000269897 Protein coding,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:22317931..22318031 32194978 MeRIP-seq:(Medium) rs1274054646 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11334316 Human_Splice_Rec_1117868,Human_Splice_Rec_1117869,Human_Splice_Rec_1117876,Human_Splice_Rec_1117877,Human_Splice_Rec_1117890,Human_Splice_Rec_1117891,Human_Splice_Rec_1117896,Human_Splice_Rec_1117897,Human_Splice_Rec_1117904,Human_Splice_Rec_1117906,Human_Splice_Rec_1117907,Human_Splice_Rec_1117916,Human_Splice_Rec_1117917,Human_Splice_Rec_1117927,Human_Splice_Rec_1117934,Human_Splice_Rec_1117935,Human_Splice_Rec_1117946,Human_Splice_Rec_1117947,Human_Splice_Rec_1117966,Human_Splice_Rec_1117967,Human_Splice_Rec_1117976,Human_Splice_Rec_1117977,Human_Splice_Rec_1117981,Human_Splice_Rec_1117998,Human_Splice_Rec_1117999,Human_Splice_Rec_1118006,Human_Splice_Rec_1118007,Human_Splice_Rec_1118032,Human_Splice_Rec_1118033,Human_Splice_Rec_1118036,Human_Splice_Rec_1118037 RMVar_hsa_circ_62006,RMVar_hsa_circ_127457,RMVar_hsa_circ_291858,RMVar_hsa_circ_142627,RMVar_hsa_circ_97680,RMVar_hsa_circ_142628,RMVar_hsa_circ_142629 93335 RMVar_ID_93335 Human_SNP_ID_424873202 m1A Human chr10 + 22321374 22321371 22321374 CCGCGCGCGCCCTCCCCCGAGTGCGGAGCGGGAGGAGGCGGCGGCGGCCGAGGAGGAGGAGGAGG CCGCGCGCGCCCTCCCCCGAGTGCGGAGCG___GGAGGCGGCGGCGGCCGAGGAGGAGGAGGAGG GGGA G COMMD3-BMI1,BMI1 Ensembl:ENSG00000269897,Ensembl:ENSG00000168283 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:22321285..22321465 26863196 MeRIP-seq:(Medium) rs968182324 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4135781 93336 RMVar_ID_93336 Human_SNP_ID_424873243 m1A Human chr10 - 22321434 22321429 22321435 CCTCGGCCTCCTCCTCCTCCGCCTCCGCCTCGACCTCCAACGCCTCCTCCTCCGGGGCCTCCTCC CCTCGGCCTCCTCCTCCTCCGCCTCCGCCTC______CAACGCCTCCTCCTCCGGGGCCTCCTCC GGAGGTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:22321227..22322118 26863196 MeRIP-seq:(Medium) rs1246080872 Functional Loss DEL dbSNP153 32..37 33 - - - 93337 RMVar_ID_93337 Human_SNP_ID_424873279 m1A Human chr10 + 22321491 22321491 22321491 GGCCGAGGCGCCGGAGGAGGCCGAGGCGCCGGAGCAGGAGGAGGCCGGCCGGAGGCGGCATGAGA GGCCGAGGCGCCGGAGGAGGCCGAGGCGCCGGTGCAGGAGGAGGCCGGCCGGAGGCGGCATGAGA A T COMMD3-BMI1,BMI1 Ensembl:ENSG00000269897,Ensembl:ENSG00000168283 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:22321246..22322118;chr10:22321242..22321659 26863196 MeRIP-seq:(Medium) rs1477492577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225939,Human_RBP_ID_3937689,Human_RBP_ID_4135782,Human_RBP_ID_5086606,Human_RBP_ID_5312977,Human_RBP_ID_8940369,Human_RBP_ID_9274099,Human_RBP_ID_9320834,Human_RBP_ID_17668578,Human_RBP_ID_22531401,Human_RBP_ID_26317027,Human_RBP_ID_26767684,Human_RBP_ID_27801934 93338 RMVar_ID_93338 Human_SNP_ID_424873281 m1A Human chr10 + 22321500 22321500 22321500 GCCGGAGGAGGCCGAGGCGCCGGAGCAGGAGGAGGCCGGCCGGAGGCGGCATGAGACGAGCGTGG GCCGGAGGAGGCCGAGGCGCCGGAGCAGGAGGCGGCCGGCCGGAGGCGGCATGAGACGAGCGTGG A C COMMD3-BMI1,BMI1 Ensembl:ENSG00000269897,Ensembl:ENSG00000168283 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:22321409..22321510 26863410 MeRIP-seq:(Medium) rs1032608497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225939,Human_RBP_ID_3937689,Human_RBP_ID_4135782,Human_RBP_ID_5086606,Human_RBP_ID_5312977,Human_RBP_ID_8940369,Human_RBP_ID_9274099,Human_RBP_ID_9320834,Human_RBP_ID_22531401,Human_RBP_ID_26317027,Human_RBP_ID_26767684,Human_RBP_ID_27801934 93339 RMVar_ID_93339 Human_SNP_ID_424927750 m1A Human chr10 - 22541956 22541954 22541957 GAGAGCCGAACAGGAGGAAGTGGAGTGTGAGGAGAACGATGGGGAGGAGGAGGGCGAGAGCGATG GAGAGCCGAACAGGAGGAAGTGGAGTGTGAG___AACGATGGGGAGGAGGAGGGCGAGAGCGATG TCTC T PIP4K2A Ensembl:ENSG00000150867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:22541907..22541988 26863196 MeRIP-seq:(Medium) rs1256733270 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4115714,Human_RBP_ID_5955770,Human_RBP_ID_23450119,Human_RBP_ID_26317028 Human_Splice_Rec_1118282,Human_Splice_Rec_1118296,Human_Splice_Rec_1118316,Human_Splice_Rec_1118328 RMVar_hsa_circ_142634,RMVar_hsa_circ_47025,RMVar_hsa_circ_142633,RMVar_hsa_circ_76969,RMVar_hsa_circ_317452,RMVar_hsa_circ_318438,RMVar_hsa_circ_112978,RMVar_hsa_circ_3590,RMVar_hsa_circ_142635,RMVar_hsa_circ_32885,RMVar_hsa_circ_82944,RMVar_hsa_circ_303004,RMVar_hsa_circ_142636 93340 RMVar_ID_93340 Human_SNP_ID_424937868 m1A Human chr10 - 22578505 22578505 22578505 CAGGAAAGATGGGACGGAGTAGGAGGACTGCCAGGAGAACACAGCGTCTCAGAAGCCAAGGGAGG CAGGAAAGATGGGACGGAGTAGGAGGACTGCCGGGAGAACACAGCGTCTCAGAAGCCAAGGGAGG T C PIP4K2A Ensembl:ENSG00000150867 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:22578499..22578608 26863196 MeRIP-seq:(Medium) rs1475320729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112978,RMVar_hsa_circ_3590,RMVar_hsa_circ_142635,RMVar_hsa_circ_29641,RMVar_hsa_circ_355251,RMVar_hsa_circ_356562,RMVar_hsa_circ_142638,RMVar_hsa_circ_312981,RMVar_hsa_circ_331633,RMVar_hsa_circ_364370,RMVar_hsa_circ_374124,RMVar_hsa_circ_60069,RMVar_hsa_circ_142640,RMVar_hsa_circ_142641 93341 RMVar_ID_93341 Human_SNP_ID_424941711 m1A Human chr10 + 22592577 22592565 22592578 TCCTGGAGGGTGGACAAGGACGGGCTCTGAGTAGGGGCTCTGCTGACATCATTCACTCCAAGATC TCCTGGAGGGTGGACAAGGAC_____________GGGCTCTGCTGACATCATTCACTCCAAGATC CGGGCTCTGAGTAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:22592563..22592675 26863196 MeRIP-seq:(Medium) rs1210858506 Functional Loss DEL dbSNP153 22..34 33 - - - 93342 RMVar_ID_93342 Human_SNP_ID_424974079 m1A Human chr10 - 22714514 22714496 22714515 GCAGGATACGGGCCGGGGCGCGAGCCGAGCGCAGTCTGCCGGGCCGAGCGGGCGGAGCGAGCCGA GCAGGATACGGGCCGGGGCGCGAGCCGAGCG___________________GGCGGAGCGAGCCGA CCGCTCGGCCCGGCAGACTG C PIP4K2A Ensembl:ENSG00000150867 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:22714317..22714575 26863196 MeRIP-seq:(Medium) rs1054709355 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_4136191 93343 RMVar_ID_93343 Human_SNP_ID_425042838 m1A Human chr10 - 22990165 22990164 22990166 TAAGTATGCTTCAAATTGGAAGTGGGGGGGGGAAATCACACAATATAAAGATTTCCTCTGAAAAT TAAGTATGCTTCAAATTGGAAGTGGGGGGGG__AATCACACAATATAAAGATTTCCTCTGAAAAT TTC T AL139815.1 Ensembl:ENSG00000286924 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:22990083..22990168 26863410 MeRIP-seq:(Medium) rs772484221 Functional Loss DEL dbSNP153 32..33 33 - - - 93344 RMVar_ID_93344 Human_SNP_ID_425042840 m1A Human chr10 - 22990165 22990165 22990165 TAAGTATGCTTCAAATTGGAAGTGGGGGGGGGAAATCACACAATATAAAGATTTCCTCTGAAAAT TAAGTATGCTTCAAATTGGAAGTGGGGGGGGGGAATCACACAATATAAAGATTTCCTCTGAAAAT T C AL139815.1 Ensembl:ENSG00000286924 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:22990083..22990168 26863410 MeRIP-seq:(Medium) rs569148074 Functional Loss SNV dbSNP153 33..33 33 - - - 93345 RMVar_ID_93345 Human_SNP_ID_425067769 m1A Human chr10 - 23095619 23095619 23095619 TTCCGAGGGTCAGGCCCCGGAGCAACCAGAGGAGCCGCGCCATGACGCCCGCTCCGGCGCCGCTC TTCCGAGGGTCAGGCCCCGGAGCAACCAGAGGGGCCGCGCCATGACGCCCGCTCCGGCGCCGCTC T C AL139815.1 Ensembl:ENSG00000286924 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr10:23095576..23095780;chr10:23095551..23104250 26863196 MeRIP-seq:(Medium) rs1392670303 Functional Loss SNV dbSNP153 33..33 33 - - - 93346 RMVar_ID_93346 Human_SNP_ID_425067820 m1A Human chr10 + 23095721 23095721 23095721 CGGCGGGCCCGGCACCGGGCCGGGACTGGGGGAGGCAGGTAGGACGCGGGTCCCGCAGGCCCCGC CGGCGGGCCCGGCACCGGGCCGGGACTGGGGGGGGCAGGTAGGACGCGGGTCCCGCAGGCCCCGC A G MSRB2 Ensembl:ENSG00000148450 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:23095652..23104167 26863410 MeRIP-seq:(Medium) rs911851386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136192,Human_RBP_ID_9320514 Human_Splice_Rec_1118579 93347 RMVar_ID_93347 Human_SNP_ID_425155571 m1A Human chr10 - 23439508 23439508 23439508 GCGGCGGGTGGCGCGGGGGCGGCGGCCGTGGGACCCGGGGCCCCGGCGGGGTAGTGGGTGCAGAC GCGGCGGGTGGCGCGGGGGCGGCGGCCGTGGGGCCCGGGGCCCCGGCGGGGTAGTGGGTGCAGAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:23439457..23439806 32194978 MeRIP-seq:(Medium) rs915361482 Functional Loss SNV dbSNP153 33..33 33 - - - 93348 RMVar_ID_93348 Human_SNP_ID_425155572 m1A Human chr10 - 23439508 23439508 23439508 GCGGCGGGTGGCGCGGGGGCGGCGGCCGTGGGACCCGGGGCCCCGGCGGGGTAGTGGGTGCAGAC GCGGCGGGTGGCGCGGGGGCGGCGGCCGTGGGCCCCGGGGCCCCGGCGGGGTAGTGGGTGCAGAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:23439457..23439806 32194978 MeRIP-seq:(Medium) rs915361482 Functional Loss SNV dbSNP153 33..33 33 - - - 93349 RMVar_ID_93349 Human_SNP_ID_425155610 m1A Human chr10 + 23439577 23439577 23439577 ACCCCCTTCAAGGTCTCGCTGCAGCCCCCGGGAGCCGCCGGCGCCGCGCCCGAGCCCGAGACCGG ACCCCCTTCAAGGTCTCGCTGCAGCCCCCGGGGGCCGCCGGCGCCGCGCCCGAGCCCGAGACCGG A G OTUD1 Ensembl:ENSG00000165312 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:23439476..23439856 26863410 MeRIP-seq:(Medium) rs1310601816 Functional Loss SNV dbSNP153 33..33 33 - - - 93350 RMVar_ID_93350 Human_SNP_ID_425155809 m1A Human chr10 - 23439953 23439953 23439953 GCAGTCGGGCCGCAGCAGCTCCTCCAGGAGCCAGGCCGAGGAGCCCCGCCGCGGCGGGACCGGGG GCAGTCGGGCCGCAGCAGCTCCTCCAGGAGCCGGGCCGAGGAGCCCCGCCGCGGCGGGACCGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:23439904..23440054 32194978 MeRIP-seq:(Medium) rs983276142 Functional Loss SNV dbSNP153 33..33 33 - - - 93351 RMVar_ID_93351 Human_SNP_ID_425156010 m1A Human chr10 + 23440352 23440352 23440352 AGAAGCTGGCCCTATACCTGGCCGAGGTGGAGAAGCAGGACAAGTATCTGCGGCAGAGGAATAAG AGAAGCTGGCCCTATACCTGGCCGAGGTGGAGCAGCAGGACAAGTATCTGCGGCAGAGGAATAAG A C OTUD1 Ensembl:ENSG00000165312 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:23440153..23440402 32194978 MeRIP-seq:(Medium) rs1220832315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_982684,Human_RBP_ID_17774878 93352 RMVar_ID_93352 Human_SNP_ID_425436098 m1A Human chr10 - 24546042 24546042 24546042 GAGCCATTAGAGACAGAAGGGATGAGGGAGGCAGAGTGAGCAGGTGGTCCTGTTTGGGGGCTGAG GAGCCATTAGAGACAGAAGGGATGAGGGAGGCGGAGTGAGCAGGTGGTCCTGTTTGGGGGCTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:24545991..24546085 26863196 MeRIP-seq:(Medium) rs752079976 Functional Loss SNV dbSNP153 33..33 33 - - - 93353 RMVar_ID_93353 Human_SNP_ID_425436165 m1A Human chr10 + 24546215 24546215 24546215 TCCTTCTCCTGCCTCCTCCGTCTCACTGAATCAAGGTGCCAAGGGCACCAGGACCATCCATACTC TCCTTCTCCTGCCTCCTCCGTCTCACTGAATCTAGGTGCCAAGGGCACCAGGACCATCCATACTC A T KIAA1217 Ensembl:ENSG00000120549 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:24546167..24546262 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_17230068,Human_RBP_ID_18930784 Human_miRNA_ID_414819 93354 RMVar_ID_93354 Human_SNP_ID_425446728 m1A Human chr10 - 24584646 24584646 24584646 GGAGATCCCCAGACAGAGAACCCAAGCACACGAGAAATAGCCACGACCGACACACCTTTGTCTCT GGAGATCCCCAGACAGAGAACCCAAGCACACGGGAAATAGCCACGACCGACACACCTTTGTCTCT T C ARHGAP21 Ensembl:ENSG00000107863 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:24584526..24584754 26863196 MeRIP-seq:(Medium) rs1234285835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5545588,Human_RBP_ID_11336026,Human_RBP_ID_17230069 93355 RMVar_ID_93355 Human_SNP_ID_425447183 m1A Human chr10 - 24585752 24585750 24585753 AACCCTCACCACCACACAACTCAAAACACAACAAGTCACCAACTCTCAGCTGTCGCTTTGCCATC AACCCTCACCACCACACAACTCAAAACACAA___GTCACCAACTCTCAGCTGTCGCTTTGCCATC CTTG C ARHGAP21 Ensembl:ENSG00000107863 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:24585701..24585900 26863196 MeRIP-seq:(Medium) rs776553614 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17343296,Human_RBP_ID_17774919,Human_RBP_ID_18524971,Human_RBP_ID_26316150,Human_RBP_ID_27405332,Human_RBP_ID_27801936 93356 RMVar_ID_93356 Human_SNP_ID_425460850 m1A Human chr10 + 24636998 24636998 24636998 CATAGAGCAGGCATTCAATAAATAATTATTCAATGAATTAATACATTTATTATTTAGTTTAAATT CATAGAGCAGGCATTCAATAAATAATTATTCAGTGAATTAATACATTTATTATTTAGTTTAAATT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:24636996..24637199 26863196 MeRIP-seq:(Medium) rs761826494 Functional Loss SNV dbSNP153 33..33 33 - - - 93357 RMVar_ID_93357 Human_SNP_ID_425477405 m1A Human chr10 - 24703641 24703640 24703641 TGGGAAGTGGGAGAGTGGCCATCATGTTTCTCAGGTTGCATACTGAGAATTCTGCAAGGTAACAT TGGGAAGTGGGAGAGTGGCCATCATGTTTCTC_GGTTGCATACTGAGAATTCTGCAAGGTAACAT CT C ARHGAP21 Ensembl:ENSG00000107863 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:24703639..24703742 26863196 MeRIP-seq:(Medium) rs1475379705 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2959,RMVar_hsa_circ_347323,RMVar_hsa_circ_363963,RMVar_hsa_circ_142683 93358 RMVar_ID_93358 Human_SNP_ID_425477411 m1A Human chr10 + 24703666 24703666 24703666 TGCAACCTGAGAAACATGATGGCCACTCTCCCACTTCCCATGGTATCATTTCTTTTGTCTGTCTC TGCAACCTGAGAAACATGATGGCCACTCTCCCGCTTCCCATGGTATCATTTCTTTTGTCTGTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:24703660..24703770 26863196 MeRIP-seq:(Medium) rs1272171168 Functional Loss SNV dbSNP153 33..33 33 - - - 93359 RMVar_ID_93359 Human_SNP_ID_425478314 m1A Human chr10 + 24707524 24707524 24707524 CCTCTTCAACACCACCCTTTCTCCCAAGCTCCAAATCTGCGTGACTAAACACTTGCTAAGCACAT CCTCTTCAACACCACCCTTTCTCCCAAGCTCCCAATCTGCGTGACTAAACACTTGCTAAGCACAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:24707515..24707819 26863196 MeRIP-seq:(Medium) rs975900499 Functional Loss SNV dbSNP153 33..33 33 - - - 93360 RMVar_ID_93360 Human_SNP_ID_425481936 m1A Human chr10 - 24722281 24722281 24722281 AAAGTTCATGACCTTTAACTTCTCGTTTTCCTAGGATCTCTCTAGGAGCTGACACTCGAACCTTC AAAGTTCATGACCTTTAACTTCTCGTTTTCCTGGGATCTCTCTAGGAGCTGACACTCGAACCTTC T C ARHGAP21 Ensembl:ENSG00000107863 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:24722226..24722300 26863196 MeRIP-seq:(Medium) rs1046325626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11337357,Human_RBP_ID_24801835 93361 RMVar_ID_93361 Human_SNP_ID_425482411 m1A Human chr10 + 24723708 24723681 24723709 GCCGCCGCCGCCGCCGCCGCCGCCGCGCTCCGAGGCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA GCCGCC____________________________GCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA CGCCGCCGCCGCCGCCGCCGCGCTCCGAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:24723551..24723804 26863196 MeRIP-seq:(Medium) rs1484227221 Functional Loss DEL dbSNP153 7..34 33 - - - 93362 RMVar_ID_93362 Human_SNP_ID_425482412 m1A Human chr10 + 24723708 24723687 24723709 GCCGCCGCCGCCGCCGCCGCCGCCGCGCTCCGAGGCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA GCCGCCGCCGCC______________________GCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA CGCCGCCGCCGCCGCGCTCCGAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:24723551..24723804 26863196 MeRIP-seq:(Medium) rs1273008353 Functional Loss DEL dbSNP153 13..34 33 - - - 93363 RMVar_ID_93363 Human_SNP_ID_425482414 m1A Human chr10 + 24723708 24723690 24723709 GCCGCCGCCGCCGCCGCCGCCGCCGCGCTCCGAGGCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA GCCGCCGCCGCCGCC___________________GCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA CGCCGCCGCCGCGCTCCGAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:24723551..24723804 26863196 MeRIP-seq:(Medium) rs1316738879 Functional Loss DEL dbSNP153 16..34 33 - - - 93364 RMVar_ID_93364 Human_SNP_ID_425482416 m1A Human chr10 + 24723708 24723693 24723709 GCCGCCGCCGCCGCCGCCGCCGCCGCGCTCCGAGGCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA GCCGCCGCCGCCGCCGCC________________GCCGCCGCCCCCGGCCGGCCGCTCCCAGGCA CGCCGCCGCGCTCCGAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:24723551..24723804 26863196 MeRIP-seq:(Medium) rs1031277529 Functional Loss DEL dbSNP153 19..34 33 - - - 93365 RMVar_ID_93365 Human_SNP_ID_425482677 m1A Human chr10 + 24724562 24724562 24724562 GAGCGAATTTGGCGCGGCTAGCGGAACTGTGGAGAGGCGGCTGCGCTTCTCTGTCCGCCACACTC GAGCGAATTTGGCGCGGCTAGCGGAACTGTGGGGAGGCGGCTGCGCTTCTCTGTCCGCCACACTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:24724519..24724597 26863196 MeRIP-seq:(Medium) rs987117371 Functional Loss SNV dbSNP153 33..33 33 - - - 93366 RMVar_ID_93366 Human_SNP_ID_425537678 m1A Human chr10 - 24944942 24944942 24944942 CTTGAAAGAGAGCAGCTGCTGAAGCAGAGGGAAGAGGAAGAGTGCCAGGAATGAGTCAGACAAGG CTTGAAAGAGAGCAGCTGCTGAAGCAGAGGGAGGAGGAAGAGTGCCAGGAATGAGTCAGACAAGG T C PRTFDC1 Ensembl:ENSG00000099256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:24944936..24945119 26863196 MeRIP-seq:(Medium) rs928139520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142693,RMVar_hsa_circ_106590 93367 RMVar_ID_93367 Human_SNP_ID_425539444 m1A Human chr10 - 24952549 24952549 24952549 AGAAACATGGCCGGGAGCAGCGAGGAGGCGCCAGACTACGGGCGAGGCGTCGTGGTAAATGCAAA AGAAACATGGCCGGGAGCAGCGAGGAGGCGCCGGACTACGGGCGAGGCGTCGTGGTAAATGCAAA T C PRTFDC1 Ensembl:ENSG00000099256 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:24942363..24952554 26863196 MeRIP-seq:(Medium) rs760528354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225067 Human_Splice_Rec_1119431,Human_Splice_Rec_1119447,Human_Splice_Rec_1119461 RMVar_hsa_circ_142693,RMVar_hsa_circ_106590 93368 RMVar_ID_93368 Human_SNP_ID_425554874 m1A Human chr10 + 25016674 25016674 25016674 CACAGGCGCAGAGTCCACTGCGCGGGGGCGGGACCGGGGAGCTAGCTGCAGGTACGGTGCTCCGT CACAGGCGCAGAGTCCACTGCGCGGGGGCGGGGCCGGGGAGCTAGCTGCAGGTACGGTGCTCCGT A G AL512598.2,THNSL1 Ensembl:ENSG00000285859,Ensembl:ENSG00000185875 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:25016624..25016733 26863196 MeRIP-seq:(Medium) rs1280550632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136194,Human_RBP_ID_5957041 Human_Splice_Rec_1119519 93369 RMVar_ID_93369 Human_SNP_ID_425554875 m1A Human chr10 + 25016674 25016674 25016674 CACAGGCGCAGAGTCCACTGCGCGGGGGCGGGACCGGGGAGCTAGCTGCAGGTACGGTGCTCCGT CACAGGCGCAGAGTCCACTGCGCGGGGGCGGGTCCGGGGAGCTAGCTGCAGGTACGGTGCTCCGT A T AL512598.2,THNSL1 Ensembl:ENSG00000285859,Ensembl:ENSG00000185875 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:25016624..25016733 26863196 MeRIP-seq:(Medium) rs1280550632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136194,Human_RBP_ID_5957041 Human_Splice_Rec_1119519 93370 RMVar_ID_93370 Human_SNP_ID_425713172 m1A Human chr10 + 25638540 25638540 25638540 CTGCCCGCTTTGTTCCCTAAATAGGGACTTGTATGAATGGCCCCACGAAGGTTCAGCTGTCTCTT CTGCCCGCTTTGTTCCCTAAATAGGGACTTGTGTGAATGGCCCCACGAAGGTTCAGCTGTCTCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr10:25638493..25638608;chr10:25638454..25638586;chr10:25638434..25638600 26863196 MeRIP-seq:(Medium) rs1288371189 Functional Loss SNV dbSNP153 33..33 33 - - - 93371 RMVar_ID_93371 Human_SNP_ID_425713173 m1A Human chr10 - 25638545 25638545 25638545 GAAGTAAGAGACAGCTGAACCTTCGTGGGGCCATTCATACAAGTCCCTATTTAGGGAACAAAGCG GAAGTAAGAGACAGCTGAACCTTCGTGGGGCCGTTCATACAAGTCCCTATTTAGGGAACAAAGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:25638484..25638620 26863196 MeRIP-seq:(Medium) rs570231371 Functional Loss SNV dbSNP153 33..33 33 - - - 93372 RMVar_ID_93372 Human_SNP_ID_425977968 m1A Human chr10 - 26697718 26697718 26697718 GGAGCAGCCGCGCCGCCACCGCCACCAGCGCGAGGCCATGGTCGGAGTCTGAAAGTCGCGGCAGG GGAGCAGCCGCGCCGCCACCGCCACCAGCGCGGGGCCATGGTCGGAGTCTGAAAGTCGCGGCAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr10:26697714..26697842;chr10:26697671..26704706 26863196 MeRIP-seq:(Medium) rs1172253611 Functional Loss SNV dbSNP153 33..33 33 - - - 93373 RMVar_ID_93373 Human_SNP_ID_426000069 m1A Human chr10 - 26789784 26789784 26789784 ACAGTGCACACTGGGGCCTACTGGAGGGTGAAAGGTGGGAAGAGGGAGAGGACCAGGAAAAACCT ACAGTGCACACTGGGGCCTACTGGAGGGTGAAGGGTGGGAAGAGGGAGAGGACCAGGAAAAACCT T C ABI1 Ensembl:ENSG00000136754 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:26789782..26789890 26863196 MeRIP-seq:(Medium) rs567499188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60583,RMVar_hsa_circ_315843,RMVar_hsa_circ_65317,RMVar_hsa_circ_352130 93374 RMVar_ID_93374 Human_SNP_ID_426017468 m1A Human chr10 - 26860830 26860830 26860830 TGGCAGAGCTGCAGATGTTACTAGAGGAGGAGATCCCGTCTGGCAAGAGGGCGCTGATCGAGAGT TGGCAGAGCTGCAGATGTTACTAGAGGAGGAGGTCCCGTCTGGCAAGAGGGCGCTGATCGAGAGT T C ABI1 Ensembl:ENSG00000136754 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:26860793..26860956 26863196 MeRIP-seq:(Medium) rs1327209239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5958088,Human_RBP_ID_11339221,Human_RBP_ID_17775152,Human_RBP_ID_18416093,Human_RBP_ID_26316157 Human_Splice_Rec_1120223,Human_Splice_Rec_1120241,Human_Splice_Rec_1120263,Human_Splice_Rec_1120283,Human_Splice_Rec_1120301,Human_Splice_Rec_1120319,Human_Splice_Rec_1120335,Human_Splice_Rec_1120353,Human_Splice_Rec_1120369,Human_Splice_Rec_1120381,Human_Splice_Rec_1120399,Human_Splice_Rec_1120421 Human_miRNA_ID_2709859,Human_miRNA_ID_2709860 RMVar_hsa_circ_118821,RMVar_hsa_circ_121568,RMVar_hsa_circ_142747,RMVar_hsa_circ_142748 93375 RMVar_ID_93375 Human_SNP_ID_426017474 m1A Human chr10 - 26860843 26860843 26860843 GAGGGGTGGAAAATGGCAGAGCTGCAGATGTTACTAGAGGAGGAGATCCCGTCTGGCAAGAGGGC GAGGGGTGGAAAATGGCAGAGCTGCAGATGTTTCTAGAGGAGGAGATCCCGTCTGGCAAGAGGGC T A ABI1 Ensembl:ENSG00000136754 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:26823215..26861040;chr10:26823249..26861042 26863196 MeRIP-seq:(Medium) rs201126139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4116136,Human_RBP_ID_18416093,Human_RBP_ID_26316157 Human_Splice_Rec_1120223,Human_Splice_Rec_1120241,Human_Splice_Rec_1120263,Human_Splice_Rec_1120283,Human_Splice_Rec_1120301,Human_Splice_Rec_1120319,Human_Splice_Rec_1120335,Human_Splice_Rec_1120353,Human_Splice_Rec_1120369,Human_Splice_Rec_1120381,Human_Splice_Rec_1120399,Human_Splice_Rec_1120421 Human_miRNA_ID_3084241,Human_miRNA_ID_3084242 RMVar_hsa_circ_118821,RMVar_hsa_circ_121568,RMVar_hsa_circ_142747,RMVar_hsa_circ_142748 93376 RMVar_ID_93376 Human_SNP_ID_426017475 m1A Human chr10 - 26860843 26860843 26860843 GAGGGGTGGAAAATGGCAGAGCTGCAGATGTTACTAGAGGAGGAGATCCCGTCTGGCAAGAGGGC GAGGGGTGGAAAATGGCAGAGCTGCAGATGTTGCTAGAGGAGGAGATCCCGTCTGGCAAGAGGGC T C ABI1 Ensembl:ENSG00000136754 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:26823215..26861040;chr10:26823249..26861042 26863196 MeRIP-seq:(Medium) rs201126139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4116136,Human_RBP_ID_18416093,Human_RBP_ID_26316157 Human_Splice_Rec_1120223,Human_Splice_Rec_1120241,Human_Splice_Rec_1120263,Human_Splice_Rec_1120283,Human_Splice_Rec_1120301,Human_Splice_Rec_1120319,Human_Splice_Rec_1120335,Human_Splice_Rec_1120353,Human_Splice_Rec_1120369,Human_Splice_Rec_1120381,Human_Splice_Rec_1120399,Human_Splice_Rec_1120421 Human_miRNA_ID_3084241,Human_miRNA_ID_3084242 RMVar_hsa_circ_118821,RMVar_hsa_circ_121568,RMVar_hsa_circ_142747,RMVar_hsa_circ_142748 93377 RMVar_ID_93377 Human_SNP_ID_426078029 m1A Human chr10 - 27100439 27100439 27100439 GGTAACCCGGAGGGAGAGATTGGAAACCGCGGAGTTTCCTTTGGGAGGCTGCGGCCAGCCGGGGC GGTAACCCGGAGGGAGAGATTGGAAACCGCGGCGTTTCCTTTGGGAGGCTGCGGCCAGCCGGGGC T G ANKRD26 Ensembl:ENSG00000107890 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:27100089..27100472;chr10:27100165..27100458 26863196 MeRIP-seq:(Medium) rs886046949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4116253,Human_RBP_ID_18416095 Clinvar_Rec_529 RMVar_hsa_circ_121573,RMVar_hsa_circ_142788 93378 RMVar_ID_93378 Human_SNP_ID_426080924 m1A Human chr10 - 27111037 27111034 27111038 AAAAATTAAAATAAATTTAAATACAAAAAAAAATAGCCAGGTGTGGGGTGCATGCCTGGAATCCC AAAAATTAAAATAAATTTAAATACAAAAAAA____GCCAGGTGTGGGGTGCATGCCTGGAATCCC CTATT C YME1L1 Ensembl:ENSG00000136758 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1409284796 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_4141019,Human_RBP_ID_5958730,Human_RBP_ID_8172580,Human_RBP_ID_8332372,Human_RBP_ID_24803106 93379 RMVar_ID_93379 Human_SNP_ID_426080927 m1A Human chr10 - 27111037 27111036 27111037 AAAAATTAAAATAAATTTAAATACAAAAAAAAATAGCCAGGTGTGGGGTGCATGCCTGGAATCCC AAAAATTAAAATAAATTTAAATACAAAAAAAA_TAGCCAGGTGTGGGGTGCATGCCTGGAATCCC AT A YME1L1 Ensembl:ENSG00000136758 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1207223401 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4141019,Human_RBP_ID_5958730,Human_RBP_ID_8172580,Human_RBP_ID_8332372,Human_RBP_ID_24803106 93380 RMVar_ID_93380 Human_SNP_ID_426082975 m1A Human chr10 + 27119373 27119373 27119373 ATTTCTTTTCCATCAACAGCTGCTTTTAATGCAGCCTGGTTCACAAGATTCTCCAACTCTGCTCC ATTTCTTTTCCATCAACAGCTGCTTTTAATGCGGCCTGGTTCACAAGATTCTCCAACTCTGCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:27119351..27119375 26863196 MeRIP-seq:(Medium) rs762250433 Functional Loss SNV dbSNP153 33..33 33 - - - 93381 RMVar_ID_93381 Human_SNP_ID_426085830 m1A Human chr10 - 27131092 27131092 27131092 GGTGACATTTGAGATAAAATCTGAAGGAGAAGATGGAATAAACTGCATTTATCTGAGAAAGGAAC GGTGACATTTGAGATAAAATCTGAAGGAGAAGGTGGAATAAACTGCATTTATCTGAGAAAGGAAC T C YME1L1 Ensembl:ENSG00000136758 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:27131087..27131201 26863196 MeRIP-seq:(Medium) rs755458502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11340574,Human_RBP_ID_23451280 RMVar_hsa_circ_3388,RMVar_hsa_circ_20627,RMVar_hsa_circ_142789,RMVar_hsa_circ_330757,RMVar_hsa_circ_142793,RMVar_hsa_circ_18071,RMVar_hsa_circ_313501,RMVar_hsa_circ_142797,RMVar_hsa_circ_32462,RMVar_hsa_circ_142800,RMVar_hsa_circ_334406,RMVar_hsa_circ_16607,RMVar_hsa_circ_31968,RMVar_hsa_circ_48914,RMVar_hsa_circ_142801,RMVar_hsa_circ_313908,RMVar_hsa_circ_16151,RMVar_hsa_circ_142806,RMVar_hsa_circ_142809,RMVar_hsa_circ_142808,RMVar_hsa_circ_315022,RMVar_hsa_circ_327530,RMVar_hsa_circ_49978,RMVar_hsa_circ_142807 93382 RMVar_ID_93382 Human_SNP_ID_426092318 m1A Human chr10 - 27155418 27155418 27155418 CTTGCTTCCCGCGGTGGGATCCATCGCTGGACAGCATACAGCGGCCCCGCAGACACTGCCCCTCC CTTGCTTCCCGCGGTGGGATCCATCGCTGGACGGCATACAGCGGCCCCGCAGACACTGCCCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:27155351..27155634;chr10:27155351..27155575;chr10:27155351..27155535 26863196 MeRIP-seq:(Medium) rs750218603 Functional Loss SNV dbSNP153 33..33 33 - - - 93383 RMVar_ID_93383 Human_SNP_ID_426092323 m1A Human chr10 + 27155423 27155423 27155423 GGCAGTGTCTGCGGGGCCGCTGTATGCTGTCCAGCGATGGATCCCACCGCGGGAAGCAAGAAGGA GGCAGTGTCTGCGGGGCCGCTGTATGCTGTCCTGCGATGGATCCCACCGCGGGAAGCAAGAAGGA A T MASTL Ensembl:ENSG00000120539 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:27155381..27155470 26863410 MeRIP-seq:(Medium) rs922386126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4116425,Human_RBP_ID_18416228 93384 RMVar_ID_93384 Human_SNP_ID_426094813 m1A Human chr10 + 27165469 27165469 27165469 GCCTGTCTGTCTGAAACATCACAGCTTTCTCAAGGACTCGTATGCCCTATGTCTGTAGATCAAAA GCCTGTCTGTCTGAAACATCACAGCTTTCTCAGGGACTCGTATGCCCTATGTCTGTAGATCAAAA A G MASTL Ensembl:ENSG00000120539 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27165418..27167130 32194978 MeRIP-seq:(Medium) rs779042509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863656,Human_RBP_ID_1158424,Human_RBP_ID_1351668,Human_RBP_ID_1445521,Human_RBP_ID_1764830,Human_RBP_ID_3937693,Human_RBP_ID_5959151,Human_RBP_ID_8332433,Human_RBP_ID_9361156,Human_RBP_ID_11340921,Human_RBP_ID_17459230,Human_RBP_ID_18592317,Human_RBP_ID_23451369 Human_Splice_Rec_1120830,Human_Splice_Rec_1120831,Human_Splice_Rec_1120852,Human_Splice_Rec_1120853,Human_Splice_Rec_1120874,Human_Splice_Rec_1120875 Human_miRNA_ID_2695628,Human_miRNA_ID_2695629 RMVar_hsa_circ_94473,RMVar_hsa_circ_356762,RMVar_hsa_circ_366274,RMVar_hsa_circ_366834,RMVar_hsa_circ_359266,RMVar_hsa_circ_326591,RMVar_hsa_circ_295391,RMVar_hsa_circ_142823,RMVar_hsa_circ_142824,RMVar_hsa_circ_142821,RMVar_hsa_circ_142822,RMVar_hsa_circ_142829,RMVar_hsa_circ_367681,RMVar_hsa_circ_142828,RMVar_hsa_circ_278209,RMVar_hsa_circ_66739 93385 RMVar_ID_93385 Human_SNP_ID_426098568 m1A Human chr10 - 27180967 27180967 27180967 AAATTCAAACAAGCAAACTCCAAGTGCCCACCAGTCTACCGCAGGACCTGTAATCGAAGAGGAAA AAATTCAAACAAGCAAACTCCAAGTGCCCACCGGTCTACCGCAGGACCTGTAATCGAAGAGGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27173125..27180968 32194978 MeRIP-seq:(Medium) rs757596656 Functional Loss SNV dbSNP153 33..33 33 - - - 93386 RMVar_ID_93386 Human_SNP_ID_426105708 m1A Human chr10 - 27208437 27208437 27208437 GCTTATTTTTGCCTCTTAAAATAGGACATAGGATGCAACACTTGAGCGAAGGAACCAAGGGCCGG GCTTATTTTTGCCTCTTAAAATAGGACATAGGGTGCAACACTTGAGCGAAGGAACCAAGGGCCGG T C ACBD5 Ensembl:ENSG00000107897 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:27208312..27208494;chr10:27208388..27210856 26863196 MeRIP-seq:(Medium) rs751272846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862231,Human_RBP_ID_9360217,Human_RBP_ID_26316164 Human_Splice_Rec_1120906,Human_Splice_Rec_1120928,Human_Splice_Rec_1120950,Human_Splice_Rec_1120974,Human_Splice_Rec_1120998,Human_Splice_Rec_1121022 RMVar_hsa_circ_36314,RMVar_hsa_circ_73480,RMVar_hsa_circ_351282,RMVar_hsa_circ_351811,RMVar_hsa_circ_341731,RMVar_hsa_circ_74468,RMVar_hsa_circ_68572,RMVar_hsa_circ_345574,RMVar_hsa_circ_367688,RMVar_hsa_circ_142842,RMVar_hsa_circ_57280,RMVar_hsa_circ_74227,RMVar_hsa_circ_342967,RMVar_hsa_circ_354464,RMVar_hsa_circ_65506,RMVar_hsa_circ_48672 93387 RMVar_ID_93387 Human_SNP_ID_426113745 m1A Human chr10 - 27240411 27240411 27240411 GATTCCCGCCGACAGACCTTGGGACCGGGGCCAACACTGGCAGCTGGAGATGGCGGACACGAGAT GATTCCCGCCGACAGACCTTGGGACCGGGGCCCACACTGGCAGCTGGAGATGGCGGACACGAGAT T G ACBD5 Ensembl:ENSG00000107897 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:27240360..27240545 26863196 MeRIP-seq:(Medium) rs1308575643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4116559,Human_RBP_ID_8765544 Human_Splice_Rec_1120890,Human_Splice_Rec_1120891,Human_Splice_Rec_1120913,Human_Splice_Rec_1120936,Human_Splice_Rec_1120937,Human_Splice_Rec_1120958,Human_Splice_Rec_1120959,Human_Splice_Rec_1120981,Human_Splice_Rec_1121005,Human_Splice_Rec_1121028,Human_Splice_Rec_1121029,Human_Splice_Rec_1121042,Human_Splice_Rec_1121043 93388 RMVar_ID_93388 Human_SNP_ID_426113759 m1A Human chr10 - 27240432 27240432 27240432 AAGCTGGTGCTGCTGCTGCCTGATTCCCGCCGACAGACCTTGGGACCGGGGCCAACACTGGCAGC AAGCTGGTGCTGCTGCTGCCTGATTCCCGCCGGCAGACCTTGGGACCGGGGCCAACACTGGCAGC T C ACBD5 Ensembl:ENSG00000107897 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:27240385..27240504 26863196 MeRIP-seq:(Medium) rs1458983066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136205,Human_RBP_ID_8760357,Human_RBP_ID_18592365 Human_Splice_Rec_1120890,Human_Splice_Rec_1120936,Human_Splice_Rec_1120958,Human_Splice_Rec_1121028,Human_Splice_Rec_1121042 93389 RMVar_ID_93389 Human_SNP_ID_426113765 m1A Human chr10 + 27240440 27240440 27240440 TGTTGGCCCCGGTCCCAAGGTCTGTCGGCGGGAATCAGGCAGCAGCAGCACCAGCTTTCCCAAGA TGTTGGCCCCGGTCCCAAGGTCTGTCGGCGGGCATCAGGCAGCAGCAGCACCAGCTTTCCCAAGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:27240338..27240561 26863196 MeRIP-seq:(Medium) rs1414151049 Functional Loss SNV dbSNP153 33..33 33 - - - 93390 RMVar_ID_93390 Human_SNP_ID_426113766 m1A Human chr10 + 27240440 27240440 27240440 TGTTGGCCCCGGTCCCAAGGTCTGTCGGCGGGAATCAGGCAGCAGCAGCACCAGCTTTCCCAAGA TGTTGGCCCCGGTCCCAAGGTCTGTCGGCGGGTATCAGGCAGCAGCAGCACCAGCTTTCCCAAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:27240338..27240561 26863196 MeRIP-seq:(Medium) rs1414151049 Functional Loss SNV dbSNP153 33..33 33 - - - 93391 RMVar_ID_93391 Human_SNP_ID_426113889 m1A Human chr10 + 27240763 27240763 27240763 GAGCCGCTCTCCCACCCTGGGGACCCTGGCGGAGCAGCCACACCCCCCATTCCGCCGGAGTCCGT GAGCCGCTCTCCCACCCTGGGGACCCTGGCGGGGCAGCCACACCCCCCATTCCGCCGGAGTCCGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:27240631..27240814;chr10:27240622..27240776 26863196 MeRIP-seq:(Medium) rs1377019287 Functional Loss SNV dbSNP153 33..33 33 - - - 93392 RMVar_ID_93392 Human_SNP_ID_426181575 m1A Human chr10 + 27504367 27504367 27504367 GCGGCCAGCTGGGCTCGGAGCGGAACGGGGTCAGGATGGACGAGGACGTGCTAACCACCCTGAAG GCGGCCAGCTGGGCTCGGAGCGGAACGGGGTCGGGATGGACGAGGACGTGCTAACCACCCTGAAG A G RAB18 Ensembl:ENSG00000099246 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:27504301..27504450;chr10:27504205..27504485;chr10:27504266..27504486 26863196 MeRIP-seq:(Medium) rs1413098312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_806228,Human_RBP_ID_1445589,Human_RBP_ID_4116581,Human_RBP_ID_5959464,Human_RBP_ID_8760360,Human_RBP_ID_18970683,Human_RBP_ID_22886605,Human_RBP_ID_27801954 Human_Splice_Rec_1121109,Human_Splice_Rec_1121117,Human_Splice_Rec_1121125,Human_Splice_Rec_1121137,Human_Splice_Rec_1121145,Human_Splice_Rec_1121159,Human_Splice_Rec_1121169 RMVar_hsa_circ_110698,RMVar_hsa_circ_142848 93393 RMVar_ID_93393 Human_SNP_ID_426181581 m1A Human chr10 + 27504377 27504377 27504377 GGGCTCGGAGCGGAACGGGGTCAGGATGGACGAGGACGTGCTAACCACCCTGAAGATCCTCATCA GGGCTCGGAGCGGAACGGGGTCAGGATGGACGGGGACGTGCTAACCACCCTGAAGATCCTCATCA A G RAB18 Ensembl:ENSG00000099246 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:27504326..27504446 26863196 MeRIP-seq:(Medium) rs1315455064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1445589,Human_RBP_ID_4116581,Human_RBP_ID_5959465,Human_RBP_ID_8760360,Human_RBP_ID_18970683,Human_RBP_ID_22886605,Human_RBP_ID_27801954 Human_Splice_Rec_1121109,Human_Splice_Rec_1121117,Human_Splice_Rec_1121125,Human_Splice_Rec_1121137,Human_Splice_Rec_1121145,Human_Splice_Rec_1121159,Human_Splice_Rec_1121169 RMVar_hsa_circ_110698,RMVar_hsa_circ_142848 93394 RMVar_ID_93394 Human_SNP_ID_426183101 m1A Human chr10 + 27509927 27509927 27509927 ATGATACGTTTGATCCAGAACTTGCAGCAACAATAGGTAAGCCTGTGTTTAAAAATTCTATAGAA ATGATACGTTTGATCCAGAACTTGCAGCAACAGTAGGTAAGCCTGTGTTTAAAAATTCTATAGAA A G RAB18 Ensembl:ENSG00000099246 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27509876..27509950 32194978 MeRIP-seq:(Medium) rs375572465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861512,Human_RBP_ID_1764892,Human_RBP_ID_27801956 Human_Splice_Rec_1121110,Human_Splice_Rec_1121111,Human_Splice_Rec_1121118,Human_Splice_Rec_1121126,Human_Splice_Rec_1121127,Human_Splice_Rec_1121138,Human_Splice_Rec_1121139,Human_Splice_Rec_1121146,Human_Splice_Rec_1121147,Human_Splice_Rec_1121160,Human_Splice_Rec_1121161,Human_Splice_Rec_1121170,Human_Splice_Rec_1121171,Human_Splice_Rec_1121176,Human_Splice_Rec_1121177 RMVar_hsa_circ_110698,RMVar_hsa_circ_142848 93395 RMVar_ID_93395 Human_SNP_ID_426187054 m1A Human chr10 + 27526834 27526820 27526834 CTTATCAAAATTTTCATTTCTTTAAGGTGTTGACTTTAAGGTGAAAACAATTTCAGTGGATGGAA CTTATCAAAATTTTCATTT______________CTTTAAGGTGAAAACAATTTCAGTGGATGGAA TCTTTAAGGTGTTGA T RAB18 Ensembl:ENSG00000099246 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27526826..27526900 32194978 MeRIP-seq:(Medium) rs1277492062 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_28591,Human_RBP_ID_861513,Human_RBP_ID_22639245,Human_RBP_ID_23451488,Human_RBP_ID_27801957 Human_Splice_Rec_1121112,Human_Splice_Rec_1121113,Human_Splice_Rec_1121128,Human_Splice_Rec_1121129,Human_Splice_Rec_1121148,Human_Splice_Rec_1121149,Human_Splice_Rec_1121162,Human_Splice_Rec_1121163,Human_Splice_Rec_1121178,Human_Splice_Rec_1121179 RMVar_hsa_circ_142850,RMVar_hsa_circ_313164 93396 RMVar_ID_93396 Human_SNP_ID_426187065 m1A Human chr10 + 27526883 27526883 27526883 ATTTCAGTGGATGGAAATAAGGCTAAACTTGCAATATGGGTAAGAGTTTTTAAAATGTATTTTTA ATTTCAGTGGATGGAAATAAGGCTAAACTTGCGATATGGGTAAGAGTTTTTAAAATGTATTTTTA A G RAB18 Ensembl:ENSG00000099246 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:27526826..27526900;chr10:27514208..27531607 26863196 MeRIP-seq:(Medium) rs1184067133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861513,Human_RBP_ID_27801957 Human_Splice_Rec_1121112,Human_Splice_Rec_1121113,Human_Splice_Rec_1121128,Human_Splice_Rec_1121129,Human_Splice_Rec_1121148,Human_Splice_Rec_1121149,Human_Splice_Rec_1121162,Human_Splice_Rec_1121163,Human_Splice_Rec_1121178,Human_Splice_Rec_1121179 RMVar_hsa_circ_142850,RMVar_hsa_circ_313164 93397 RMVar_ID_93397 Human_SNP_ID_426193543 m1A Human chr10 + 27550888 27550888 27550888 TGGGCCTAGGAAGAGAGAAAATGGGACATGTTACAGAATGCTTTTGTGTTGATGGGAATGAGACA TGGGCCTAGGAAGAGAGAAAATGGGACATGTTGCAGAATGCTTTTGTGTTGATGGGAATGAGACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:27550837..27550926 26863196 MeRIP-seq:(Medium) rs902696053 Functional Loss SNV dbSNP153 33..33 33 - - - 93398 RMVar_ID_93398 Human_SNP_ID_426232308 m1A Human chr10 - 27711407 27711403 27711408 GAAAGAAAGAGAAAAGAAAGAAAGAAAGAAGGAAAGAAGGAAAGGAAGAAAGAAAAGAAAAAAGT GAAAGAAAGAGAAAAGAAAGAAAGAAAGAAG_____AAGGAAAGGAAGAAAGAAAAGAAAAAAGT TCTTTC T MKX Ensembl:ENSG00000150051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:27711377..27711634;chr10:27711360..27711614 26863196 MeRIP-seq:(Medium) rs1260711340 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_28851 93399 RMVar_ID_93399 Human_SNP_ID_426232309 m1A Human chr10 - 27711407 27711407 27711407 GAAAGAAAGAGAAAAGAAAGAAAGAAAGAAGGAAAGAAGGAAAGGAAGAAAGAAAAGAAAAAAGT GAAAGAAAGAGAAAAGAAAGAAAGAAAGAAGGCAAGAAGGAAAGGAAGAAAGAAAAGAAAAAAGT T G MKX Ensembl:ENSG00000150051 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:27711377..27711634;chr10:27711360..27711614 26863196 MeRIP-seq:(Medium) rs547138947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28851 93400 RMVar_ID_93400 Human_SNP_ID_426239989 m1A Human chr10 + 27743288 27743288 27743288 TGTCCTTGAGGGGCGGGCCGTCGGGAATGCCCACCTCGGGGCGGGCGTGAGGACTGTCCAGGACA TGTCCTTGAGGGGCGGGCCGTCGGGAATGCCCTCCTCGGGGCGGGCGTGAGGACTGTCCAGGACA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:27743232..27743382 32194978 MeRIP-seq:(Medium) rs771310883 Functional Loss SNV dbSNP153 33..33 33 - - - 93401 RMVar_ID_93401 Human_SNP_ID_426240105 m1A Human chr10 - 27743463 27743463 27743463 GCCGAGCCCCGCTGCGGAGCTCCCGGCGGCCCAGCCCCGAGGCTCTGCGGCCGCGCCGCGCGTCC GCCGAGCCCCGCTGCGGAGCTCCCGGCGGCCCGGCCCCGAGGCTCTGCGGCCGCGCCGCGCGTCC T C MKX Ensembl:ENSG00000150051 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:27743422..27743537 26863196 MeRIP-seq:(Medium) rs755161075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1121196,Human_Splice_Rec_1121208,Human_Splice_Rec_1121228 RMVar_hsa_circ_57167 93402 RMVar_ID_93402 Human_SNP_ID_426240106 m1A Human chr10 - 27743463 27743463 27743463 GCCGAGCCCCGCTGCGGAGCTCCCGGCGGCCCAGCCCCGAGGCTCTGCGGCCGCGCCGCGCGTCC GCCGAGCCCCGCTGCGGAGCTCCCGGCGGCCCCGCCCCGAGGCTCTGCGGCCGCGCCGCGCGTCC T G MKX Ensembl:ENSG00000150051 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:27743422..27743537 26863196 MeRIP-seq:(Medium) rs755161075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1121196,Human_Splice_Rec_1121208,Human_Splice_Rec_1121228 RMVar_hsa_circ_57167 93403 RMVar_ID_93403 Human_SNP_ID_426240819 m1A Human chr10 + 27745788 27745788 27745788 CTCGAGACTAGGCGCACTCCCATCCCCGCCGCATGTTCTCCACGCGGGCTCCAGCGCGCTCACCA CTCGAGACTAGGCGCACTCCCATCCCCGCCGCTTGTTCTCCACGCGGGCTCCAGCGCGCTCACCA A T MKX-AS1 Ensembl:ENSG00000230500 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr10:27745668..27745803;chr10:27743381..27745961 26863196 MeRIP-seq:(Medium) rs1378575368 Functional Loss SNV dbSNP153 33..33 33 - - - 93404 RMVar_ID_93404 Human_SNP_ID_426257176 m1A Human chr10 + 27813197 27813197 27813197 TCATAACTTTCCCACTTCTCTTGGCTTTACTGATGCTATCCCCTATCTAAAATGCCTTCCCATCC TCATAACTTTCCCACTTCTCTTGGCTTTACTGTTGCTATCCCCTATCTAAAATGCCTTCCCATCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:27813147..27813244 26863196 MeRIP-seq:(Medium) rs1564386984 Functional Loss SNV dbSNP153 33..33 33 - - - 93405 RMVar_ID_93405 Human_SNP_ID_426373885 m1A Human chr10 + 28302952 28302952 28302952 CCGGGCCCGGAGGCAAGGAGGCAGCGACCGCCACCGCCGCAGAGGACAATCGGGAGCCAGCGGGC CCGGGCCCGGAGGCAAGGAGGCAGCGACCGCCGCCGCCGCAGAGGACAATCGGGAGCCAGCGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:28302904..28302996 26863196 MeRIP-seq:(Medium) rs1255770533 Functional Loss SNV dbSNP153 33..33 33 - - - 93406 RMVar_ID_93406 Human_SNP_ID_426431758 m1A Human chr10 + 28532252 28532252 28532252 TGTTCCCAAGGAACTCATCTCCCTAAATTTCCAGTCTCAAGCGCCGCTTTCATTCCCTGCCCCGA TGTTCCCAAGGAACTCATCTCCCTAAATTTCCCGTCTCAAGCGCCGCTTTCATTCCCTGCCCCGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:28532246..28532373 26863196 MeRIP-seq:(Medium) rs1564364995 Functional Loss SNV dbSNP153 33..33 33 - - - 93407 RMVar_ID_93407 Human_SNP_ID_426432263 m1A Human chr10 + 28533215 28533215 28533215 GAGGAGGAGGAGAAGAAGGACCAGGCGGCGGCAGCAGCGGCGGCGGCGGGGGGAGGAGGGGAGGA GAGGAGGAGGAGAAGAAGGACCAGGCGGCGGCGGCAGCGGCGGCGGCGGGGGGAGGAGGGGAGGA A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:28533151..28533300 26863410 MeRIP-seq:(Medium) rs1056997887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135789,Human_RBP_ID_17066900,Human_RBP_ID_18456051 RMVar_hsa_circ_83153,RMVar_hsa_circ_122678,RMVar_hsa_circ_142861,RMVar_hsa_circ_142862 93408 RMVar_ID_93408 Human_SNP_ID_426432276 m1A Human chr10 + 28533236 28533236 28533236 CAGGCGGCGGCAGCAGCGGCGGCGGCGGGGGGAGGAGGGGAGGAGGCGGCGGAGCAGGAGGAGGA CAGGCGGCGGCAGCAGCGGCGGCGGCGGGGGGGGGAGGGGAGGAGGCGGCGGAGCAGGAGGAGGA A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:28533151..28533275 26863410 MeRIP-seq:(Medium) rs1036685921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225039,Human_RBP_ID_805879,Human_RBP_ID_4135789,Human_RBP_ID_18456051 RMVar_hsa_circ_83153,RMVar_hsa_circ_122678,RMVar_hsa_circ_142861,RMVar_hsa_circ_142862 93409 RMVar_ID_93409 Human_SNP_ID_426432290 m1A Human chr10 + 28533268 28533268 28533268 AGGAGGGGAGGAGGCGGCGGAGCAGGAGGAGGAGAAGGCGGAGGAGGCAGTCGCTCTCCGCGGGG AGGAGGGGAGGAGGCGGCGGAGCAGGAGGAGGGGAAGGCGGAGGAGGCAGTCGCTCTCCGCGGGG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:28533171..28533283 26863410 MeRIP-seq:(Medium) rs1280004202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5340406,Human_RBP_ID_26317051 RMVar_hsa_circ_83153,RMVar_hsa_circ_122678,RMVar_hsa_circ_142861,RMVar_hsa_circ_142862 93410 RMVar_ID_93410 Human_SNP_ID_426432299 m1A Human chr10 - 28533286 28533286 28533286 ACGACGCGTCCGGCTCAGCCCCGCGGAGAGCGACTGCCTCCTCCGCCTTCTCCTCCTCCTGCTCC ACGACGCGTCCGGCTCAGCCCCGCGGAGAGCGGCTGCCTCCTCCGCCTTCTCCTCCTCCTGCTCC T C WAC-AS1,WAC-AS1:2,WAC-AS1:3,WAC-AS1:4 RNACentral:URS0000D5AE7F,RNACentral:URS0000D58195,RNACentral:URS0000D5DE00,RNACentral:URS0000D5C177 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr10:28532793..28533638;chr10:28532692..28534125;chr10:28532692..28533825;chr10:28533151..28533350 26863196 MeRIP-seq:(Medium) rs1173707181 Functional Loss SNV dbSNP153 33..33 33 - - - 93411 RMVar_ID_93411 Human_SNP_ID_426432458 m1A Human chr10 - 28533563 28533559 28533563 TCGCATACATTACCATCAATGCCCGGCCTGTGAGTGTGTGTCGGGGAGGGGGGAGAGCGGCCGCG TCGCATACATTACCATCAATGCCCGGCCTGTG____TGTGTCGGGGAGGGGGGAGAGCGGCCGCG ACACT A WAC-AS1,WAC-AS1:2,WAC-AS1:3,WAC-AS1:4 RNACentral:URS0000D5AE7F,RNACentral:URS0000D58195,RNACentral:URS0000D5DE00,RNACentral:URS0000D5C177 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:28533126..28533625 26863196 MeRIP-seq:(Medium) rs753837598 Functional Loss DEL dbSNP153 33..36 33 - - - 93412 RMVar_ID_93412 Human_SNP_ID_426432655 m1A Human chr10 - 28533862 28533862 28533862 CCGAGCGCCCCAGCGCCGAGCCCCGCACGCACACGGCACAAACCCGGAGCCTCCGGAAGGGCCGG CCGAGCGCCCCAGCGCCGAGCCCCGCACGCACGCGGCACAAACCCGGAGCCTCCGGAAGGGCCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:28533858..28533967 32194978 MeRIP-seq:(Medium) rs573100307 Functional Loss SNV dbSNP153 33..33 33 - - - 93413 RMVar_ID_93413 Human_SNP_ID_426432724 m1A Human chr10 - 28533962 28533960 28533962 AAAAACAGGAAGAGAAGGCAGCGACATAAGACACGGCGCGGGTGGGGGGCCGGGGAGGAAGAAAA AAAAACAGGAAGAGAAGGCAGCGACATAAGAC__GGCGCGGGTGGGGGGCCGGGGAGGAAGAAAA CGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:28533953..28534077 26863196 MeRIP-seq:(Medium) rs1256093749 Functional Loss DEL dbSNP153 33..34 33 - - - 93414 RMVar_ID_93414 Human_SNP_ID_426433367 m1A Human chr10 + 28535624 28535624 28535624 AGTAGCGGTGATCACAGACATGAAAAGATGCGAGACGCCGGAGATCCTTCACCACCAAATAAAAT AGTAGCGGTGATCACAGACATGAAAAGATGCGGGACGCCGGAGATCCTTCACCACCAAATAAAAT A G WAC Ensembl:ENSG00000095787 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:28535518..28535705;chr10:28535498..28535694 26863196 MeRIP-seq:(Medium) rs774802587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1445699,Human_RBP_ID_1765002,Human_RBP_ID_3347556,Human_RBP_ID_4141157,Human_RBP_ID_5960645,Human_RBP_ID_8244582,Human_RBP_ID_8332682,Human_RBP_ID_11342648,Human_RBP_ID_17226696,Human_RBP_ID_17459287,Human_RBP_ID_18524985,Human_RBP_ID_18592493,Human_RBP_ID_22880504 Human_Splice_Rec_1121658,Human_Splice_Rec_1121692,Human_Splice_Rec_1121696,Human_Splice_Rec_1121702,Human_Splice_Rec_1121708,Human_Splice_Rec_1121732,Human_Splice_Rec_1121758,Human_Splice_Rec_1121794,Human_Splice_Rec_1121808,Human_Splice_Rec_1121824,Human_Splice_Rec_1121840,Human_Splice_Rec_1121844,Human_Splice_Rec_1121854,Human_Splice_Rec_1121858 RMVar_hsa_circ_24199,RMVar_hsa_circ_83153,RMVar_hsa_circ_122678,RMVar_hsa_circ_319068,RMVar_hsa_circ_100516,RMVar_hsa_circ_142861,RMVar_hsa_circ_142862,RMVar_hsa_circ_362963,RMVar_hsa_circ_142863,RMVar_hsa_circ_357747,RMVar_hsa_circ_299770,RMVar_hsa_circ_311914,RMVar_hsa_circ_48352,RMVar_hsa_circ_142864,RMVar_hsa_circ_142866,RMVar_hsa_circ_142867,RMVar_hsa_circ_142865 93415 RMVar_ID_93415 Human_SNP_ID_426440997 m1A Human chr10 + 28560835 28560835 28560835 TGAAGGGGTGTTGCCAGCTTTGACCAGTAGGCAGATTTTCCTAATTTGTACACTCCTGCTGTAGA TGAAGGGGTGTTGCCAGCTTTGACCAGTAGGCCGATTTTCCTAATTTGTACACTCCTGCTGTAGA A C WAC Ensembl:ENSG00000095787 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:28560833..28561029 26863196 MeRIP-seq:(Medium) rs902985710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24199,RMVar_hsa_circ_83153,RMVar_hsa_circ_122678,RMVar_hsa_circ_100516,RMVar_hsa_circ_142861,RMVar_hsa_circ_142862,RMVar_hsa_circ_362963,RMVar_hsa_circ_142863,RMVar_hsa_circ_357747,RMVar_hsa_circ_299770,RMVar_hsa_circ_311914,RMVar_hsa_circ_48352,RMVar_hsa_circ_142866,RMVar_hsa_circ_142867,RMVar_hsa_circ_142865 93416 RMVar_ID_93416 Human_SNP_ID_426453978 m1A Human chr10 + 28608280 28608280 28608280 TCTGGACTGAACCCCACATCTGCACCTCCAACATCTGCTTCAGCGGTCCCTGTTTCTCCTGTTCC TCTGGACTGAACCCCACATCTGCACCTCCAACGTCTGCTTCAGCGGTCCCTGTTTCTCCTGTTCC A G WAC Ensembl:ENSG00000095787 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:28608230..28608348 26863196 MeRIP-seq:(Medium) rs1408979486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376419,Human_RBP_ID_4116850,Human_RBP_ID_17226715,Human_RBP_ID_17343391,Human_RBP_ID_17459298,Human_RBP_ID_18592575,Human_RBP_ID_22880624,Human_RBP_ID_24805137,Human_RBP_ID_26394394,Human_RBP_ID_27405430 Human_Splice_Rec_1121668,Human_Splice_Rec_1121716,Human_Splice_Rec_1121742,Human_Splice_Rec_1121766,Human_Splice_Rec_1121818,Human_Splice_Rec_1121834,Human_Splice_Rec_1121876,Human_Splice_Rec_1121900,Human_Splice_Rec_1121924,Human_Splice_Rec_1121936 RMVar_hsa_circ_24199,RMVar_hsa_circ_122678,RMVar_hsa_circ_142861,RMVar_hsa_circ_357747,RMVar_hsa_circ_48352,RMVar_hsa_circ_142867,RMVar_hsa_circ_372424,RMVar_hsa_circ_90294,RMVar_hsa_circ_142870,RMVar_hsa_circ_142871,RMVar_hsa_circ_377287,RMVar_hsa_circ_378310,RMVar_hsa_circ_352921,RMVar_hsa_circ_103059,RMVar_hsa_circ_29550,RMVar_hsa_circ_142873,RMVar_hsa_circ_142872,RMVar_hsa_circ_42828,RMVar_hsa_circ_53960,RMVar_hsa_circ_331927,RMVar_hsa_circ_312253 93417 RMVar_ID_93417 Human_SNP_ID_426455825 m1A Human chr10 + 28614619 28614619 28614619 GCAAGGACCAGTGTCACAGTCAGCCACACAGCAGCCTGTAACTGCTGACAAGCAGCAAGGTCATG GCAAGGACCAGTGTCACAGTCAGCCACACAGCTGCCTGTAACTGCTGACAAGCAGCAAGGTCATG A T WAC Ensembl:ENSG00000095787 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:28614540..28614646 26863196 MeRIP-seq:(Medium) rs774042989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376427,Human_RBP_ID_17229175,Human_RBP_ID_18592589 Human_Splice_Rec_1121674,Human_Splice_Rec_1121675,Human_Splice_Rec_1121722,Human_Splice_Rec_1121723,Human_Splice_Rec_1121748,Human_Splice_Rec_1121749,Human_Splice_Rec_1121772,Human_Splice_Rec_1121773,Human_Splice_Rec_1121884,Human_Splice_Rec_1121885,Human_Splice_Rec_1121908,Human_Splice_Rec_1121909,Human_Splice_Rec_1121928 Human_miRNA_ID_1043597 RMVar_hsa_circ_122678,RMVar_hsa_circ_142861,RMVar_hsa_circ_357747,RMVar_hsa_circ_48352,RMVar_hsa_circ_142867,RMVar_hsa_circ_90294,RMVar_hsa_circ_142871,RMVar_hsa_circ_377287,RMVar_hsa_circ_29550,RMVar_hsa_circ_53960,RMVar_hsa_circ_36982,RMVar_hsa_circ_339513 93418 RMVar_ID_93418 Human_SNP_ID_426472187 m1A Human chr10 - 28677550 28677550 28677550 AAGAGAGTAGGGTCTCCACAGCACGCAAGGGTATCCGCCGCAGCTCCCGCCCGCGCCAGCCCAGG AAGAGAGTAGGGTCTCCACAGCACGCAAGGGTCTCCGCCGCAGCTCCCGCCCGCGCCAGCCCAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:28677501..28677773 26863196 MeRIP-seq:(Medium) rs1437502095 Functional Loss SNV dbSNP153 33..33 33 - - - 93419 RMVar_ID_93419 Human_SNP_ID_426472196 m1A Human chr10 - 28677555 28677555 28677555 CAGCGAAGAGAGTAGGGTCTCCACAGCACGCAAGGGTATCCGCCGCAGCTCCCGCCCGCGCCAGC CAGCGAAGAGAGTAGGGTCTCCACAGCACGCAGGGGTATCCGCCGCAGCTCCCGCCCGCGCCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:28677501..28677748 26863196 MeRIP-seq:(Medium) rs924382872 Functional Loss SNV dbSNP153 33..33 33 - - - 93420 RMVar_ID_93420 Human_SNP_ID_426472219 m1A Human chr10 - 28677586 28677586 28677586 CCGGCCTTCAGTCCCCGCTAGCGGCCGTTCTCAGCGAAGAGAGTAGGGTCTCCACAGCACGCAAG CCGGCCTTCAGTCCCCGCTAGCGGCCGTTCTCGGCGAAGAGAGTAGGGTCTCCACAGCACGCAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:28677536..28677765 26863196 MeRIP-seq:(Medium) rs1413413708 Functional Loss SNV dbSNP153 33..33 33 - - - 93421 RMVar_ID_93421 Human_SNP_ID_426472245 m1A Human chr10 + 28677632 28677632 28677632 AGCGGGGACTGAAGGCCGGGAGCCCACTCCCGACCCGGGGCTAGCGTGCGTCCCTAGAGTCGAGC AGCGGGGACTGAAGGCCGGGAGCCCACTCCCGGCCCGGGGCTAGCGTGCGTCCCTAGAGTCGAGC A G BAMBI Ensembl:ENSG00000095739 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:28677538..28677648 26863410 MeRIP-seq:(Medium) rs1391300047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748361,Human_RBP_ID_4136209,Human_RBP_ID_5138239,Human_RBP_ID_5520099,Human_RBP_ID_22431676 93422 RMVar_ID_93422 Human_SNP_ID_426661675 m1A Human chr10 + 29422126 29422126 29422126 GGTGGTGAAATGGCCCTGTGTGAATGTGGAAGACCAGCAGATTGGAGGTGGAATTGGCCTCAGTG GGTGGTGAAATGGCCCTGTGTGAATGTGGAAGCCCAGCAGATTGGAGGTGGAATTGGCCTCAGTG A C SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:29422049..29422186 26863196 MeRIP-seq:(Medium) rs1482097741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5962121,Human_RBP_ID_9340640,Human_RBP_ID_17104908,Human_RBP_ID_17204662,Human_RBP_ID_22708226,Human_RBP_ID_23452432,Human_RBP_ID_26398240 93423 RMVar_ID_93423 Human_SNP_ID_426666625 m1A Human chr10 + 29439252 29439224 29439252 CGGATTGAGTCAGGGTGGAGCAGGTAATCCACATGAGTCAGGGTGGAGTAGGTAATCGGAATGAG CGGAT____________________________TGAGTCAGGGTGGAGTAGGTAATCGGAATGAG TTGAGTCAGGGTGGAGCAGGTAATCCACA T SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:29439066..29439323 26863196 MeRIP-seq:(Medium) rs1318280325 Functional Loss DEL dbSNP153 6..33 33 - - - 93424 RMVar_ID_93424 Human_SNP_ID_426666635 m1A Human chr10 + 29439252 29439251 29439253 CGGATTGAGTCAGGGTGGAGCAGGTAATCCACATGAGTCAGGGTGGAGTAGGTAATCGGAATGAG CGGATTGAGTCAGGGTGGAGCAGGTAATCCAC__GAGTCAGGGTGGAGTAGGTAATCGGAATGAG CAT C SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:29439066..29439323 26863196 MeRIP-seq:(Medium) rs1415879537 Functional Loss DEL dbSNP153 33..34 33 - - - 93425 RMVar_ID_93425 Human_SNP_ID_426674335 m1A Human chr10 + 29470478 29470478 29470478 GGGCACCTCTCCACGCACGCAGTACAGCCGCCACTCACCTGCAGGGGGCACCGGCGGCGCGGAGG GGGCACCTCTCCACGCACGCAGTACAGCCGCCCCTCACCTGCAGGGGGCACCGGCGGCGCGGAGG A C SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29470364..29470521 26863196 MeRIP-seq:(Medium) rs1227213128 Functional Loss SNV dbSNP153 33..33 33 - - - 93426 RMVar_ID_93426 Human_SNP_ID_426674508 m1A Human chr10 + 29471100 29471100 29471100 CCCAGCTTATAAAAATTCTTTCCAAGAGAGGGAAAGGCAAAGTCGAATTCCAGCAGTAAAAGTGA CCCAGCTTATAAAAATTCTTTCCAAGAGAGGGCAAGGCAAAGTCGAATTCCAGCAGTAAAAGTGA A C SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:29471098..29471207 26863196 MeRIP-seq:(Medium) rs1225290469 Functional Loss SNV dbSNP153 33..33 33 - - - 93427 RMVar_ID_93427 Human_SNP_ID_426674874 m1A Human chr10 - 29472704 29472689 29472705 CAGATCCAAGGCCACCTAAAGCTACTGGCCTCACAACCCCATGGCCTTATAACCCCAGGGCCTGC CAGATCCAAGGCCACCTAAAGCTACTGGCCT________________TATAACCCCAGGGCCTGC AAGGCCATGGGGTTGTG A SVIL Ensembl:ENSG00000197321 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29472702..29472797 26863196 MeRIP-seq:(Medium) rs1370771966 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_105841 RMVar_hsa_circ_52759,RMVar_hsa_circ_96184,RMVar_hsa_circ_142884,RMVar_hsa_circ_142885,RMVar_hsa_circ_126998,RMVar_hsa_circ_363075 93428 RMVar_ID_93428 Human_SNP_ID_426687876 m1A Human chr10 - 29523764 29523764 29523764 AACAAGGGAATGTTGAGAGAATATGGAGAGACAGAAAGCAAGAGAGCTTTGACAGGTCGAGACAG AACAAGGGAATGTTGAGAGAATATGGAGAGACGGAAAGCAAGAGAGCTTTGACAGGTCGAGACAG T C SVIL Ensembl:ENSG00000197321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29523714..29523797 26863196 MeRIP-seq:(Medium) rs1319189951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22771,RMVar_hsa_circ_142885,RMVar_hsa_circ_126998,RMVar_hsa_circ_64840,RMVar_hsa_circ_361448,RMVar_hsa_circ_367567,RMVar_hsa_circ_15950,RMVar_hsa_circ_55417,RMVar_hsa_circ_18215,RMVar_hsa_circ_67161,RMVar_hsa_circ_334511,RMVar_hsa_circ_11657,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_310324,RMVar_hsa_circ_362967 93429 RMVar_ID_93429 Human_SNP_ID_426694982 m1A Human chr10 + 29550670 29550670 29550670 GGGGCTCCGGGAGGCTGCCTGCTGCAGGGAGGAGCTGTGGGCGTGCTTGGGGGACCGTGGCACTT GGGGCTCCGGGAGGCTGCCTGCTGCAGGGAGGCGCTGTGGGCGTGCTTGGGGGACCGTGGCACTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29550611..29550692 26863196 MeRIP-seq:(Medium) rs755414793 Functional Loss SNV dbSNP153 33..33 33 - - - 93430 RMVar_ID_93430 Human_SNP_ID_426709083 m1A Human chr10 + 29610196 29610196 29610196 CTCTATCTCCAATCAGTTCCTCAACCTGGGCAATTCTTCCCTCACGCCCCACCCTCGTCCCTTCC CTCTATCTCCAATCAGTTCCTCAACCTGGGCAGTTCTTCCCTCACGCCCCACCCTCGTCCCTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:29610168..29610370 26863196 MeRIP-seq:(Medium) rs1404509607 Functional Loss SNV dbSNP153 33..33 33 - - - 93431 RMVar_ID_93431 Human_SNP_ID_426726973 m1A Human chr10 - 29686653 29686653 29686653 ATCCTATGATTTTTTTAAAACTTTTCTCCCCCAGATTCTGGCTACATTGGAGATTGGTTGCTTTC ATCCTATGATTTTTTTAAAACTTTTCTCCCCCTGATTCTGGCTACATTGGAGATTGGTTGCTTTC T A SVIL Ensembl:ENSG00000197321 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29686651..29686675 26863196 MeRIP-seq:(Medium) rs1379623634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142889,RMVar_hsa_circ_118204 93432 RMVar_ID_93432 Human_SNP_ID_426739092 m1A Human chr10 - 29735328 29735328 29735328 GTGGCCCGGGGAGTGGCGCGCCAGTGATCAGAACTACGACATCGCCCGGTTCCTTTCCCGACACC GTGGCCCGGGGAGTGGCGCGCCAGTGATCAGATCTACGACATCGCCCGGTTCCTTTCCCGACACC T A SVIL Ensembl:ENSG00000197321 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:29735326..29735411 26863196 MeRIP-seq:(Medium) rs1316026218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364540,Human_RBP_ID_8172128,Human_RBP_ID_26775181 RMVar_hsa_circ_142889,RMVar_hsa_circ_118204 93433 RMVar_ID_93433 Human_SNP_ID_426739502 m1A Human chr10 + 29736652 29736652 29736652 CTTCCCGGGGGTGCGCCCACACTCACGCGCCCACACTCGCGTCCCCACCTTCCCCCCCGTCTCAC CTTCCCGGGGGTGCGCCCACACTCACGCGCCCCCACTCGCGTCCCCACCTTCCCCCCCGTCTCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:29736647..29736956 26863196 MeRIP-seq:(Medium) rs1010588811 Functional Loss SNV dbSNP153 33..33 33 - - - 93434 RMVar_ID_93434 Human_SNP_ID_426739566 m1A Human chr10 + 29736834 29736834 29736834 GCTGGCTCTCGAGGAGGTGTGGGCCCCGGGAAAGTCGGCCAGGGCCACTGTCGCCGTCGCCGCCG GCTGGCTCTCGAGGAGGTGTGGGCCCCGGGAAGGTCGGCCAGGGCCACTGTCGCCGTCGCCGCCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:29736725..29736933 26863196 MeRIP-seq:(Medium) rs1467834528 Functional Loss SNV dbSNP153 33..33 33 - - - 93435 RMVar_ID_93435 Human_SNP_ID_458121326 m1A Human chr11 + 20054160 20054160 20054160 GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGACACCGCTGCCAATTCCCCCTTTTCCTCTGGCT GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGGCACCGCTGCCAATTCCCCCTTTTCCTCTGGCT A G NAV2 Ensembl:ENSG00000166833 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:20054076..20054230 26863196 MeRIP-seq:(Medium) rs766953407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1220000,Human_Splice_Rec_1220001,Human_Splice_Rec_1220074,Human_Splice_Rec_1220075,Human_Splice_Rec_1220150,Human_Splice_Rec_1220151,Human_Splice_Rec_1220224,Human_Splice_Rec_1220225,Human_Splice_Rec_1220298,Human_Splice_Rec_1220299,Human_Splice_Rec_1220374,Human_Splice_Rec_1220375,Human_Splice_Rec_1220444,Human_Splice_Rec_1220445,Human_Splice_Rec_1220494,Human_Splice_Rec_1220495 Human_miRNA_ID_2945643,Human_miRNA_ID_2945644 RMVar_hsa_circ_484,RMVar_hsa_circ_107272,RMVar_hsa_circ_148647,RMVar_hsa_circ_36342,RMVar_hsa_circ_82910,RMVar_hsa_circ_148654,RMVar_hsa_circ_94749,RMVar_hsa_circ_148658,RMVar_hsa_circ_11275,RMVar_hsa_circ_100448,RMVar_hsa_circ_148660,RMVar_hsa_circ_83061,RMVar_hsa_circ_148663,RMVar_hsa_circ_527,RMVar_hsa_circ_29438,RMVar_hsa_circ_70211,RMVar_hsa_circ_322464,RMVar_hsa_circ_11838,RMVar_hsa_circ_22991,RMVar_hsa_circ_31331,RMVar_hsa_circ_50864,RMVar_hsa_circ_25909,RMVar_hsa_circ_148672,RMVar_hsa_circ_300836,RMVar_hsa_circ_312011,RMVar_hsa_circ_364513,RMVar_hsa_circ_377604,RMVar_hsa_circ_339899,RMVar_hsa_circ_307639,RMVar_hsa_circ_7249,RMVar_hsa_circ_20683,RMVar_hsa_circ_148674,RMVar_hsa_circ_148675,RMVar_hsa_circ_148673 93436 RMVar_ID_93436 Human_SNP_ID_458121327 m1A Human chr11 + 20054160 20054160 20054160 GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGACACCGCTGCCAATTCCCCCTTTTCCTCTGGCT GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGTCACCGCTGCCAATTCCCCCTTTTCCTCTGGCT A T NAV2 Ensembl:ENSG00000166833 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:20054076..20054230 26863196 MeRIP-seq:(Medium) rs766953407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1220000,Human_Splice_Rec_1220001,Human_Splice_Rec_1220074,Human_Splice_Rec_1220075,Human_Splice_Rec_1220150,Human_Splice_Rec_1220151,Human_Splice_Rec_1220224,Human_Splice_Rec_1220225,Human_Splice_Rec_1220298,Human_Splice_Rec_1220299,Human_Splice_Rec_1220374,Human_Splice_Rec_1220375,Human_Splice_Rec_1220444,Human_Splice_Rec_1220445,Human_Splice_Rec_1220494,Human_Splice_Rec_1220495 Human_miRNA_ID_2945643,Human_miRNA_ID_2945644 RMVar_hsa_circ_484,RMVar_hsa_circ_107272,RMVar_hsa_circ_148647,RMVar_hsa_circ_36342,RMVar_hsa_circ_82910,RMVar_hsa_circ_148654,RMVar_hsa_circ_94749,RMVar_hsa_circ_148658,RMVar_hsa_circ_11275,RMVar_hsa_circ_100448,RMVar_hsa_circ_148660,RMVar_hsa_circ_83061,RMVar_hsa_circ_148663,RMVar_hsa_circ_527,RMVar_hsa_circ_29438,RMVar_hsa_circ_70211,RMVar_hsa_circ_322464,RMVar_hsa_circ_11838,RMVar_hsa_circ_22991,RMVar_hsa_circ_31331,RMVar_hsa_circ_50864,RMVar_hsa_circ_25909,RMVar_hsa_circ_148672,RMVar_hsa_circ_300836,RMVar_hsa_circ_312011,RMVar_hsa_circ_364513,RMVar_hsa_circ_377604,RMVar_hsa_circ_339899,RMVar_hsa_circ_307639,RMVar_hsa_circ_7249,RMVar_hsa_circ_20683,RMVar_hsa_circ_148674,RMVar_hsa_circ_148675,RMVar_hsa_circ_148673 93437 RMVar_ID_93437 Human_SNP_ID_458122812 m1A Human chr11 + 20060548 20060548 20060548 TCTAGAACGCAGGGCATTGCTAAGGAGGGTGGATGTACATGCTGATATAGGGACAGCTTAGAGCA TCTAGAACGCAGGGCATTGCTAAGGAGGGTGGGTGTACATGCTGATATAGGGACAGCTTAGAGCA A G NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:20060542..20060692 26863196 MeRIP-seq:(Medium) rs1390563400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_484,RMVar_hsa_circ_107272,RMVar_hsa_circ_148647,RMVar_hsa_circ_82910,RMVar_hsa_circ_148654,RMVar_hsa_circ_94749,RMVar_hsa_circ_148658,RMVar_hsa_circ_83061,RMVar_hsa_circ_148663,RMVar_hsa_circ_527,RMVar_hsa_circ_29438,RMVar_hsa_circ_11838,RMVar_hsa_circ_31331,RMVar_hsa_circ_148672,RMVar_hsa_circ_300836,RMVar_hsa_circ_312011,RMVar_hsa_circ_364513,RMVar_hsa_circ_377604,RMVar_hsa_circ_339899,RMVar_hsa_circ_307639,RMVar_hsa_circ_20683,RMVar_hsa_circ_148674,RMVar_hsa_circ_148675,RMVar_hsa_circ_148673 93438 RMVar_ID_93438 Human_SNP_ID_458122874 m1A Human chr11 - 20060840 20060833 20060840 GACCTCTCCTTCTTCCCTTATATGTTCTTGTTACACTATGAATTCTGCACTGCTCTCCCAAGCTT GACCTCTCCTTCTTCCCTTATATGTTCTTGTT_______GAATTCTGCACTGCTCTCCCAAGCTT CATAGTGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:20060796..20060861 26863196 MeRIP-seq:(Medium) rs1042042323 Functional Loss DEL dbSNP153 33..39 33 - - - 93439 RMVar_ID_93439 Human_SNP_ID_458198064 m1A Human chr11 - 20364052 20364052 20364052 GCGGCTCCCCGGCCATCGCCCGCACCTGAGCCAGCAGACCCATCGGAAGGGGCCCGAGCTGGAGG GCGGCTCCCCGGCCATCGCCCGCACCTGAGCCGGCAGACCCATCGGAAGGGGCCCGAGCTGGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:20364049..20364256 26863196 MeRIP-seq:(Medium) rs936495386 Functional Loss SNV dbSNP153 33..33 33 - - - 93440 RMVar_ID_93440 Human_SNP_ID_458203944 m1A Human chr11 + 20388043 20388041 20388044 TGTGTTAGGCGGCCGGGGCGCTGTGGAGAATGAGGAGGACCTGCCAGAACTGTCGGACAGCGGGG TGTGTTAGGCGGCCGGGGCGCTGTGGAGAAT___GAGGACCTGCCAGAACTGTCGGACAGCGGGG TGAG T PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:20387750..20388100 26863196 MeRIP-seq:(Medium) rs1565188827 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_227249,Human_RBP_ID_750705,Human_RBP_ID_871383,Human_RBP_ID_5344951,Human_RBP_ID_9362068,Human_RBP_ID_11582815,Human_RBP_ID_23499005 Human_Splice_Rec_1220690 RMVar_hsa_circ_438,RMVar_hsa_circ_63978,RMVar_hsa_circ_110608,RMVar_hsa_circ_40294,RMVar_hsa_circ_148688 93441 RMVar_ID_93441 Human_SNP_ID_458203945 m1A Human chr11 + 20388043 20388043 20388043 TGTGTTAGGCGGCCGGGGCGCTGTGGAGAATGAGGAGGACCTGCCAGAACTGTCGGACAGCGGGG TGTGTTAGGCGGCCGGGGCGCTGTGGAGAATGTGGAGGACCTGCCAGAACTGTCGGACAGCGGGG A T PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:20387750..20388100 26863196 MeRIP-seq:(Medium) rs748806306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227249,Human_RBP_ID_750705,Human_RBP_ID_871383,Human_RBP_ID_5344951,Human_RBP_ID_9362068,Human_RBP_ID_11582815,Human_RBP_ID_23499005 Human_Splice_Rec_1220690 RMVar_hsa_circ_438,RMVar_hsa_circ_63978,RMVar_hsa_circ_110608,RMVar_hsa_circ_40294,RMVar_hsa_circ_148688 93442 RMVar_ID_93442 Human_SNP_ID_458203961 m1A Human chr11 + 20388076 20388076 20388076 GGAGGACCTGCCAGAACTGTCGGACAGCGGGGACGAGGCCGCCTGGGAGGATGAGGACGATGCAG GGAGGACCTGCCAGAACTGTCGGACAGCGGGGTCGAGGCCGCCTGGGAGGATGAGGACGATGCAG A T PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:20388026..20388126 32194978 MeRIP-seq:(Medium) rs760910891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227249,Human_RBP_ID_750705,Human_RBP_ID_871383,Human_RBP_ID_9362068,Human_RBP_ID_18973407 Human_Splice_Rec_1220690,Human_Splice_Rec_1220691,Human_Splice_Rec_1220719 RMVar_hsa_circ_438,RMVar_hsa_circ_63978,RMVar_hsa_circ_110608,RMVar_hsa_circ_40294,RMVar_hsa_circ_148688 93443 RMVar_ID_93443 Human_SNP_ID_458420856 m1A Human chr11 + 21228714 21228712 21228714 CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCCCACCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCC__CCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT CCA C NELL1 Ensembl:ENSG00000165973 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:21228708..21228835 26863196 MeRIP-seq:(Medium) rs1381127881 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_24353,RMVar_hsa_circ_13859 93444 RMVar_ID_93444 Human_SNP_ID_458420863 m1A Human chr11 + 21228714 21228714 21228714 CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCCCACCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCCCCCCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT A C NELL1 Ensembl:ENSG00000165973 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:21228708..21228835 26863196 MeRIP-seq:(Medium) rs1280047949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24353,RMVar_hsa_circ_13859 93445 RMVar_ID_93445 Human_SNP_ID_458420864 m1A Human chr11 + 21228714 21228714 21228714 CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCCCACCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT CCCTCCCCTCCCCTCTCCTTCCCTCCCCTCCCTCCCCTCCTTCCCTCCCCTCCCTCCCCTCCCCT A T NELL1 Ensembl:ENSG00000165973 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:21228708..21228835 26863196 MeRIP-seq:(Medium) rs1280047949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24353,RMVar_hsa_circ_13859 93446 RMVar_ID_93446 Human_SNP_ID_458670488 m1A Human chr11 + 22193695 22193695 22193695 GTGCTCAGCGCGAAACCGGGACTGCGGGGCAGAGTCCCCCGCCTGGGGTGAGTGGGGTTGGTTTC GTGCTCAGCGCGAAACCGGGACTGCGGGGCAGGGTCCCCCGCCTGGGGTGAGTGGGGTTGGTTTC A G ANO5 Ensembl:ENSG00000171714 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:22193649..22193873 32194978 MeRIP-seq:(Medium) rs935092077 Functional Loss SNV dbSNP153 33..33 33 - - - 93447 RMVar_ID_93447 Human_SNP_ID_458839240 m1A Human chr11 + 22829680 22829680 22829680 GGTGCTCAAGGCGCGGCCCGGCGGACGCAGGGACCTGCTCTACTCACCAGGTCCGGCGTGGGAGG GGTGCTCAAGGCGCGGCCCGGCGGACGCAGGGGCCTGCTCTACTCACCAGGTCCGGCGTGGGAGG A G AC006299.1 Ensembl:ENSG00000246225 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:22829676..22829775 32194978 MeRIP-seq:(Medium) rs1186984634 Functional Loss SNV dbSNP153 33..33 33 - - - 93448 RMVar_ID_93448 Human_SNP_ID_458839285 m1A Human chr11 - 22829748 22829748 22829748 GACCCGGTCAGGGTTCTCAAGCTGTCGTCCCTATGGGGCTGTGTTTTCCTTGTCCCGGGGAGTCC GACCCGGTCAGGGTTCTCAAGCTGTCGTCCCTCTGGGGCTGTGTTTTCCTTGTCCCGGGGAGTCC T G SVIP Ensembl:ENSG00000198168 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:22829651..22829791 26863196 MeRIP-seq:(Medium) rs764834025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393861,Human_RBP_ID_4183967,Human_RBP_ID_5235193,Human_RBP_ID_9321342,Human_RBP_ID_23499303 Human_Splice_Rec_1221295 93449 RMVar_ID_93449 Human_SNP_ID_458839291 m1A Human chr11 + 22829756 22829756 22829756 CGGGACAAGGAAAACACAGCCCCATAGGGACGACAGCTTGAGAACCCTGACCGGGTCCGGCCCAG CGGGACAAGGAAAACACAGCCCCATAGGGACGTCAGCTTGAGAACCCTGACCGGGTCCGGCCCAG A T AC006299.1 Ensembl:ENSG00000246225 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:22829642..22829784 26863196 MeRIP-seq:(Medium) rs779494185 Functional Loss SNV dbSNP153 33..33 33 - - - 93450 RMVar_ID_93450 Human_SNP_ID_458839311 m1A Human chr11 - 22829779 22829779 22829779 CCGCGCAGTTAGCGCCGCCTGGCCTGGGCCGGACCCGGTCAGGGTTCTCAAGCTGTCGTCCCTAT CCGCGCAGTTAGCGCCGCCTGGCCTGGGCCGGGCCCGGTCAGGGTTCTCAAGCTGTCGTCCCTAT T C SVIP Ensembl:ENSG00000198168 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:22829671..22829799 26863196 MeRIP-seq:(Medium) rs1420652968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393861,Human_RBP_ID_4183968,Human_RBP_ID_9321343,Human_RBP_ID_23499303 Human_Splice_Rec_1221295 93451 RMVar_ID_93451 Human_SNP_ID_458845720 m1A Human chr11 - 22853692 22853692 22853692 CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCATCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCTTCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT T A CCDC179 Ensembl:ENSG00000255359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:22853674..22853739 26863196 MeRIP-seq:(Medium) rs7395367 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12168,GWAS_ID_12169,GWAS_ID_12170,GWAS_ID_12171,GWAS_ID_12172,GWAS_ID_12173,GWAS_ID_12174,GWAS_ID_12175,GWAS_ID_12176,GWAS_ID_12177,GWAS_ID_12178,GWAS_ID_12179,GWAS_ID_12180,GWAS_ID_12181,GWAS_ID_12182,GWAS_ID_12183,GWAS_ID_12184,GWAS_ID_12185,GWAS_ID_12186,GWAS_ID_12187,GWAS_ID_12188 93452 RMVar_ID_93452 Human_SNP_ID_458845721 m1A Human chr11 - 22853692 22853692 22853692 CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCATCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCGTCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT T C CCDC179 Ensembl:ENSG00000255359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:22853674..22853739 26863196 MeRIP-seq:(Medium) rs7395367 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12168,GWAS_ID_12169,GWAS_ID_12170,GWAS_ID_12171,GWAS_ID_12172,GWAS_ID_12173,GWAS_ID_12174,GWAS_ID_12175,GWAS_ID_12176,GWAS_ID_12177,GWAS_ID_12178,GWAS_ID_12179,GWAS_ID_12180,GWAS_ID_12181,GWAS_ID_12182,GWAS_ID_12183,GWAS_ID_12184,GWAS_ID_12185,GWAS_ID_12186,GWAS_ID_12187,GWAS_ID_12188 93453 RMVar_ID_93453 Human_SNP_ID_458845722 m1A Human chr11 - 22853692 22853692 22853692 CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCATCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCCTCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT T G CCDC179 Ensembl:ENSG00000255359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:22853674..22853739 26863196 MeRIP-seq:(Medium) rs7395367 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12168,GWAS_ID_12169,GWAS_ID_12170,GWAS_ID_12171,GWAS_ID_12172,GWAS_ID_12173,GWAS_ID_12174,GWAS_ID_12175,GWAS_ID_12176,GWAS_ID_12177,GWAS_ID_12178,GWAS_ID_12179,GWAS_ID_12180,GWAS_ID_12181,GWAS_ID_12182,GWAS_ID_12183,GWAS_ID_12184,GWAS_ID_12185,GWAS_ID_12186,GWAS_ID_12187,GWAS_ID_12188 93454 RMVar_ID_93454 Human_SNP_ID_460042195 m1A Human chr11 + 27339032 27339032 27339032 AGGCTGGTTCTGGATAGGAATTTCCACTGTAAAAACCTAAAATTATTGAAAAATCAGATCAAAAC AGGCTGGTTCTGGATAGGAATTTCCACTGTAAGAACCTAAAATTATTGAAAAATCAGATCAAAAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:27338993..27348924 32194978 MeRIP-seq:(Medium) rs1029193907 Functional Loss SNV dbSNP153 33..33 33 - - - 93455 RMVar_ID_93455 Human_SNP_ID_460042747 m1A Human chr11 + 27341422 27341422 27341422 ACCTTTTCTTTCTTCTTCCTCTCACATTCTTCAGCATTTTTTTTCTTTAACCATTCTTGATATTT ACCTTTTCTTTCTTCTTCCTCTCACATTCTTCCGCATTTTTTTTCTTTAACCATTCTTGATATTT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:27341420..27341549 26863196 MeRIP-seq:(Medium) rs745647709 Functional Loss SNV dbSNP153 33..33 33 - - - 93456 RMVar_ID_93456 Human_SNP_ID_460042779 m1A Human chr11 - 27341520 27341517 27341521 AGAAAAGAAAAGAAAGAGAACAAAAAATTAATAAAGAAATGGAGGAAAAAGCAGCAAAGGAACTG AGAAAAGAAAAGAAAGAGAACAAAAAATTAA____GAAATGGAGGAAAAAGCAGCAAAGGAACTG CTTTA C CCDC34 Ensembl:ENSG00000109881 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:27340751..27348924 26863196 MeRIP-seq:(Medium) rs1307488368 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_32144,Human_RBP_ID_986650,Human_RBP_ID_17464233,Human_RBP_ID_18525805 Human_Splice_Rec_1222028,Human_Splice_Rec_1222042 RMVar_hsa_circ_67491 93457 RMVar_ID_93457 Human_SNP_ID_460042785 m1A Human chr11 - 27341533 27341533 27341533 CTATTTTTATTTAAGAAAAGAAAAGAAAGAGAACAAAAAATTAATAAAGAAATGGAGGAAAAAGC CTATTTTTATTTAAGAAAAGAAAAGAAAGAGAGCAAAAAATTAATAAAGAAATGGAGGAAAAAGC T C CCDC34 Ensembl:ENSG00000109881 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:27341348..27341581;chr11:27341365..27348924;chr11:27341358..27348924 26863196 MeRIP-seq:(Medium) rs1565057339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32144,Human_RBP_ID_986650,Human_RBP_ID_18525805 Human_Splice_Rec_1222028,Human_Splice_Rec_1222042 RMVar_hsa_circ_67491 93458 RMVar_ID_93458 Human_SNP_ID_460044992 m1A Human chr11 - 27350382 27350382 27350382 GAAAAGAAATGGAAGAACGTGAAAAAAGAAAGATAATTGCTGAAGAAAAGCACAAGGAATGGGTT GAAAAGAAATGGAAGAACGTGAAAAAAGAAAGGTAATTGCTGAAGAAAAGCACAAGGAATGGGTT T C CCDC34 Ensembl:ENSG00000109881 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:27350284..27350420 26863196 MeRIP-seq:(Medium) rs374290862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32145,Human_RBP_ID_8229205,Human_RBP_ID_17648627,Human_RBP_ID_23499749,Human_RBP_ID_26318153 Human_Splice_Rec_1222027,Human_Splice_Rec_1222040,Human_Splice_Rec_1222041,Human_Splice_Rec_1222050 93459 RMVar_ID_93459 Human_SNP_ID_460047982 m1A Human chr11 + 27362949 27362949 27362949 TCATCATCCACGTCTTCCTCATCCTCCCCGTCACCGTCGTCCTCGTCAAACTGGAAGCTCTGGTG TCATCATCCACGTCTTCCTCATCCTCCCCGTCCCCGTCGTCCTCGTCAAACTGGAAGCTCTGGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:27362901..27363171 32194978 MeRIP-seq:(Medium) rs931126531 Functional Loss SNV dbSNP153 33..33 33 - - - 93460 RMVar_ID_93460 Human_SNP_ID_460048036 m1A Human chr11 + 27363041 27363041 27363041 GGAATTGCTGCAGCTCAGCGGCAGCGGCGGCGACGGCGAGCGCACCACCTCCAGCCCCTGCCCAC GGAATTGCTGCAGCTCAGCGGCAGCGGCGGCGGCGGCGAGCGCACCACCTCCAGCCCCTGCCCAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:27362973..27363142 26863196 MeRIP-seq:(Medium) rs375252730 Functional Loss SNV dbSNP153 33..33 33 - - - 93461 RMVar_ID_93461 Human_SNP_ID_460049070 m1A Human chr11 - 27367363 27367363 27367363 GGACTGTCCCAGCTAGAACTGTGAGAGTATACATAGGCATTACTTTATTATGTTTTCACTTGCCA GGACTGTCCCAGCTAGAACTGTGAGAGTATACGTAGGCATTACTTTATTATGTTTTCACTTGCCA T C LGR4 Ensembl:ENSG00000205213 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2447995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17681775 Human_miRNA_ID_1750846,Human_miRNA_ID_2063252,Human_miRNA_ID_2576358,Human_miRNA_ID_2900917 GWAS_ID_12189,GWAS_ID_12190,GWAS_ID_12191 RMVar_hsa_circ_101570,RMVar_hsa_circ_111858,RMVar_hsa_circ_148775,RMVar_hsa_circ_148776 93462 RMVar_ID_93462 Human_SNP_ID_460072877 m1A Human chr11 - 27472723 27472722 27472724 GAGATTGAGCCGCGGCTGGGAGACAGCGAGCCAGAGTCTGGGTGTTTGTGCGAGAGCCACGGCGG GAGATTGAGCCGCGGCTGGGAGACAGCGAGC__GAGTCTGGGTGTTTGTGCGAGAGCCACGGCGG CTG C LGR4 Ensembl:ENSG00000205213 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:27472118..27472800;chr11:27472270..27472800;chr11:27412818..27472800 26863196 MeRIP-seq:(Medium) rs1267346024 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_193687,Human_RBP_ID_752452,Human_RBP_ID_4157170,Human_RBP_ID_5520652,Human_RBP_ID_18188176,Human_RBP_ID_18416531,Human_RBP_ID_22433455,Human_RBP_ID_24542956,Human_RBP_ID_26318156,Human_RBP_ID_27803301 93463 RMVar_ID_93463 Human_SNP_ID_460072883 m1A Human chr11 - 27472731 27472731 27472731 GACGGGAAGAGATTGAGCCGCGGCTGGGAGACAGCGAGCCAGAGTCTGGGTGTTTGTGCGAGAGC GACGGGAAGAGATTGAGCCGCGGCTGGGAGACCGCGAGCCAGAGTCTGGGTGTTTGTGCGAGAGC T G LGR4 Ensembl:ENSG00000205213 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:27472324..27472825 26863196 MeRIP-seq:(Medium) rs1314707574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4157170,Human_RBP_ID_5520652,Human_RBP_ID_18188176,Human_RBP_ID_18416531,Human_RBP_ID_22433455,Human_RBP_ID_24542956,Human_RBP_ID_26318156,Human_RBP_ID_27803301 93464 RMVar_ID_93464 Human_SNP_ID_460081383 m1A Human chr11 - 27506360 27506360 27506360 CCCGAAAAGCAAACGTCACACACCCGGTTCGCACAGACTACACTCATTGCCTGTACAGCACGAGA CCCGAAAAGCAAACGTCACACACCCGGTTCGCGCAGACTACACTCATTGCCTGTACAGCACGAGA T C LIN7C Ensembl:ENSG00000148943 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:27506357..27506446 26863196 MeRIP-seq:(Medium) rs1465826319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11586654 93465 RMVar_ID_93465 Human_SNP_ID_460114782 m1A Human chr11 + 27656090 27656090 27656090 CCAGACACCTTCCCGAAGTCTTGTCTCTGGACAAGATTTCCTATGGGTCCCCTTGATCATTCGGC CCAGACACCTTCCCGAAGTCTTGTCTCTGGACGAGATTTCCTATGGGTCCCCTTGATCATTCGGC A G BDNF-AS Ensembl:ENSG00000245573 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:27656040..27656191 32194978 MeRIP-seq:(Medium) rs927052912 Functional Loss SNV dbSNP153 33..33 33 - - - 93466 RMVar_ID_93466 Human_SNP_ID_460114899 m1A Human chr11 + 27656591 27656591 27656591 CGCACTGCCGGTAAATGCAATGCCAACTCCACATAGCCTCCATTTGGCTGTTCAGTCTCATGTCA CGCACTGCCGGTAAATGCAATGCCAACTCCACGTAGCCTCCATTTGGCTGTTCAGTCTCATGTCA A G BDNF-AS Ensembl:ENSG00000245573 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:27656540..27656690 32194978 MeRIP-seq:(Medium) rs1415962525 Functional Loss SNV dbSNP153 33..33 33 - - - 93467 RMVar_ID_93467 Human_SNP_ID_460115331 m1A Human chr11 - 27658102 27658102 27658102 TTAGTGAGTGGGTAACGGCGGCAGACAAAAAGACTGCAGTGGACATGTCGGGCGGGACGGTCACA TTAGTGAGTGGGTAACGGCGGCAGACAAAAAGTCTGCAGTGGACATGTCGGGCGGGACGGTCACA T A BDNF Ensembl:ENSG00000176697 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:27658051..27658400 32194978 MeRIP-seq:(Medium) rs201468555 Functional Loss SNV dbSNP153 33..33 33 - - - 93468 RMVar_ID_93468 Human_SNP_ID_460115461 m1A Human chr11 + 27658552 27658552 27658552 GCAACCAAAGTATGAAATAACCATAGTAAGGAAAAGGATGGTCATCACTCTTCTCACCTGGTGGA GCAACCAAAGTATGAAATAACCATAGTAAGGAGAAGGATGGTCATCACTCTTCTCACCTGGTGGA A G BDNF-AS Ensembl:ENSG00000245573 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:27658501..27658638 26863196 MeRIP-seq:(Medium) rs1253363411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1222263,Human_Splice_Rec_1222275,Human_Splice_Rec_1222283,Human_Splice_Rec_1222369,Human_Splice_Rec_1222405,Human_Splice_Rec_1222421 RMVar_hsa_circ_25208 93469 RMVar_ID_93469 Human_SNP_ID_460125251 m1A Human chr11 - 27700550 27700547 27700550 CGAACGGGTATCGGTAGCGCGGGCGAGCGGGGAGCGGGGGGCGGGGGGCGGGGGGGGGGGGGCGG CGAACGGGTATCGGTAGCGCGGGCGAGCGGGG___GGGGGGCGGGGGGCGGGGGGGGGGGGGCGG CGCT C BDNF,AC103796.1 Ensembl:ENSG00000176697,Ensembl:ENSG00000255496 Protein coding,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:27700501..27700575 26863196 MeRIP-seq:(Medium) rs1432482029 Functional Loss DEL dbSNP153 33..35 33 - - - 93470 RMVar_ID_93470 Human_SNP_ID_460125254 m1A Human chr11 - 27700550 27700550 27700550 CGAACGGGTATCGGTAGCGCGGGCGAGCGGGGAGCGGGGGGCGGGGGGCGGGGGGGGGGGGGCGG CGAACGGGTATCGGTAGCGCGGGCGAGCGGGGGGCGGGGGGCGGGGGGCGGGGGGGGGGGGGCGG T C BDNF,AC103796.1 Ensembl:ENSG00000176697,Ensembl:ENSG00000255496 Protein coding,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:27700501..27700575 26863196 MeRIP-seq:(Medium) rs960321323 Functional Loss SNV dbSNP153 33..33 33 - - - 93471 RMVar_ID_93471 Human_SNP_ID_460125563 m1A Human chr11 + 27701539 27701539 27701539 GTAATACTCGCACCCCATCAGCGAGAAGCTCCATTTGATCTCGGCAGAGGCAGGGAGATTTCATG GTAATACTCGCACCCCATCAGCGAGAAGCTCCGTTTGATCTCGGCAGAGGCAGGGAGATTTCATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:27701489..27701577 26863196 MeRIP-seq:(Medium) rs985458593 Functional Loss SNV dbSNP153 33..33 33 - - - 93472 RMVar_ID_93472 Human_SNP_ID_460129582 m1A Human chr11 + 27719399 27719399 27719399 CGGAGCTAAAAGTGTTCTTCTCCACCGCCTCCAGCCGCCCAGGCCCCCTCGCCCGGCCCGCTCTC CGGAGCTAAAAGTGTTCTTCTCCACCGCCTCCGGCCGCCCAGGCCCCCTCGCCCGGCCCGCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:27719364..27719429 26863196 MeRIP-seq:(Medium) rs1460722127 Functional Loss SNV dbSNP153 33..33 33 - - - 93473 RMVar_ID_93473 Human_SNP_ID_460169613 m1A Human chr11 - 27890196 27890196 27890196 AGAAGGATGGTGACAAGAAGAAGAAGAAGACTAAGGAAAAGTACATCGACCAAGAAGAACTCAAC AGAAGGATGGTGACAAGAAGAAGAAGAAGACTGAGGAAAAGTACATCGACCAAGAAGAACTCAAC T C HSP90AA2P Ensembl:ENSG00000224411 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:27890151..27890381 26863196 MeRIP-seq:(Medium) rs1399196811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092970,Human_RBP_ID_6064018,Human_RBP_ID_8246747,Human_RBP_ID_17467191,Human_RBP_ID_18526150 93474 RMVar_ID_93474 Human_SNP_ID_460219659 m1A Human chr11 - 28097973 28097973 28097973 TTTTAATTTCAGAGAAGTATTCAAGTATTTATACAGATAGGAATCAAGATAATCAACAATGTCTG TTTTAATTTCAGAGAAGTATTCAAGTATTTATGCAGATAGGAATCAAGATAATCAACAATGTCTG T C KIF18A Ensembl:ENSG00000121621 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:28097923..28098015 26863196 MeRIP-seq:(Medium) rs1181493456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22034337,Human_RBP_ID_23500132,Human_RBP_ID_27803313 Human_Splice_Rec_1222766,Human_Splice_Rec_1222818 RMVar_hsa_circ_8134,RMVar_hsa_circ_86626,RMVar_hsa_circ_32143,RMVar_hsa_circ_148800,RMVar_hsa_circ_148804,RMVar_hsa_circ_106119,RMVar_hsa_circ_66920 93475 RMVar_ID_93475 Human_SNP_ID_460226945 m1A Human chr11 + 28127078 28127077 28127079 AGCAAGCCACTGAGTGAGTGTGCTGAAAATGCAAAGAGGGAGATGGTGCAAGATGAGGCTGGAGA AGCAAGCCACTGAGTGAGTGTGCTGAAAATGC__AGAGGGAGATGGTGCAAGATGAGGCTGGAGA CAA C METTL15 Ensembl:ENSG00000169519 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:28126936..28127104 26863196 MeRIP-seq:(Medium) rs1371697027 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_394339 RMVar_hsa_circ_88384,RMVar_hsa_circ_358017,RMVar_hsa_circ_148806,RMVar_hsa_circ_107276,RMVar_hsa_circ_370933,RMVar_hsa_circ_148808,RMVar_hsa_circ_148807 93476 RMVar_ID_93476 Human_SNP_ID_460226946 m1A Human chr11 + 28127078 28127078 28127078 AGCAAGCCACTGAGTGAGTGTGCTGAAAATGCAAAGAGGGAGATGGTGCAAGATGAGGCTGGAGA AGCAAGCCACTGAGTGAGTGTGCTGAAAATGCCAAGAGGGAGATGGTGCAAGATGAGGCTGGAGA A C METTL15 Ensembl:ENSG00000169519 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:28126936..28127104 26863196 MeRIP-seq:(Medium) rs1170635936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_394339 RMVar_hsa_circ_88384,RMVar_hsa_circ_358017,RMVar_hsa_circ_148806,RMVar_hsa_circ_107276,RMVar_hsa_circ_370933,RMVar_hsa_circ_148808,RMVar_hsa_circ_148807 93477 RMVar_ID_93477 Human_SNP_ID_33297958 m1A Human chr1 + 150010586 150010586 150010586 CGACGGCGATGGAGGTGGAGGCGGTGGTGGAGACTGCGACCGCAGCTGTTGCTCCGCACGGGATC CGACGGCGATGGAGGTGGAGGCGGTGGTGGAGCCTGCGACCGCAGCTGTTGCTCCGCACGGGATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149971191..150010725 26863196 MeRIP-seq:(Medium) rs147372021 Functional Loss SNV dbSNP153 33..33 33 - - - 93478 RMVar_ID_93478 Human_SNP_ID_33297963 m1A Human chr1 - 150010602 150010602 150010602 TCTGGCTCCAGCTCCAGATCCCGTGCGGAGCAACAGCTGCGGTCGCAGTCTCCACCACCGCCTCC TCTGGCTCCAGCTCCAGATCCCGTGCGGAGCAGCAGCTGCGGTCGCAGTCTCCACCACCGCCTCC T C OTUD7B Ensembl:ENSG00000264522 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:150010453..150010722;chr1:150010426..150010725 26863196 MeRIP-seq:(Medium) rs368490394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125515 93479 RMVar_ID_93479 Human_SNP_ID_33306314 m1A Human chr1 + 150047346 150047346 150047346 TGATTCCCTAACCACCACATTTATAACTGCAAACCTTATGCATCTCAACACTCCCCCCAACCTCC TGATTCCCTAACCACCACATTTATAACTGCAATCCTTATGCATCTCAACACTCCCCCCAACCTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150047130..150047445 26863196 MeRIP-seq:(Medium) rs1299058147 Functional Loss SNV dbSNP153 33..33 33 - - - 93480 RMVar_ID_93480 Human_SNP_ID_33311037 m1A Human chr1 + 150067880 150067880 150067880 ATTCGCCGCCATGAACGTGGTTTTTGCTGTGAAGCAGTACATTTCCAAAATGATAGAGGACAGCG ATTCGCCGCCATGAACGTGGTTTTTGCTGTGAGGCAGTACATTTCCAAAATGATAGAGGACAGCG A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:150067830..150067906 26863196 MeRIP-seq:(Medium) rs781836609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1411165,Human_RBP_ID_18415049,Human_RBP_ID_22127034,Human_RBP_ID_26840797 Human_Splice_Rec_125591,Human_Splice_Rec_125681,Human_Splice_Rec_125689,Human_Splice_Rec_125717,Human_Splice_Rec_125719,Human_Splice_Rec_125745,Human_Splice_Rec_125751,Human_Splice_Rec_125779,Human_Splice_Rec_125803 93481 RMVar_ID_93481 Human_SNP_ID_33317494 m1A Human chr1 + 150095956 150095956 150095956 GGATTATTGAAGGCAAAAATAGAAGCAGAGAGACTACTGAGGAGATGAATGCAGTAGTCCAGGTG GGATTATTGAAGGCAAAAATAGAAGCAGAGAGGCTACTGAGGAGATGAATGCAGTAGTCCAGGTG A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150095946..150096079 26863196 MeRIP-seq:(Medium) rs1196890724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6693,RMVar_hsa_circ_293143,RMVar_hsa_circ_62762,RMVar_hsa_circ_11465,RMVar_hsa_circ_42942,RMVar_hsa_circ_359182,RMVar_hsa_circ_74674,RMVar_hsa_circ_284279,RMVar_hsa_circ_336444,RMVar_hsa_circ_304965,RMVar_hsa_circ_60399 93482 RMVar_ID_93482 Human_SNP_ID_33317585 m1A Human chr1 + 150096419 150096419 150096419 AGGTAGTTATTGGATAAAGATATTTTGAATTCAAGATTTCATAGGGGGTTCAGATACTTGTAACG AGGTAGTTATTGGATAAAGATATTTTGAATTCGAGATTTCATAGGGGGTTCAGATACTTGTAACG A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150096411..150096603 26863196 MeRIP-seq:(Medium) rs587618824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6693,RMVar_hsa_circ_293143,RMVar_hsa_circ_62762,RMVar_hsa_circ_11465,RMVar_hsa_circ_42942,RMVar_hsa_circ_359182,RMVar_hsa_circ_74674,RMVar_hsa_circ_284279,RMVar_hsa_circ_336444,RMVar_hsa_circ_304965,RMVar_hsa_circ_60399 93483 RMVar_ID_93483 Human_SNP_ID_33317586 m1A Human chr1 + 150096419 150096419 150096419 AGGTAGTTATTGGATAAAGATATTTTGAATTCAAGATTTCATAGGGGGTTCAGATACTTGTAACG AGGTAGTTATTGGATAAAGATATTTTGAATTCTAGATTTCATAGGGGGTTCAGATACTTGTAACG A T VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150096411..150096603 26863196 MeRIP-seq:(Medium) rs587618824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6693,RMVar_hsa_circ_293143,RMVar_hsa_circ_62762,RMVar_hsa_circ_11465,RMVar_hsa_circ_42942,RMVar_hsa_circ_359182,RMVar_hsa_circ_74674,RMVar_hsa_circ_284279,RMVar_hsa_circ_336444,RMVar_hsa_circ_304965,RMVar_hsa_circ_60399 93484 RMVar_ID_93484 Human_SNP_ID_33330195 m1A Human chr1 + 150150872 150150872 150150872 TGAGAGACGGACGGAGAGGAAGCGCCGGCTGGAATCTCCTAACCGCCCGCTTCTCATCTTGTCCT TGAGAGACGGACGGAGAGGAAGCGCCGGCTGGGATCTCCTAACCGCCCGCTTCTCATCTTGTCCT A G PLEKHO1 Ensembl:ENSG00000023902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:150150869..150151038;chr1:150150861..150150997 26863196 MeRIP-seq:(Medium) rs1553818716 Functional Loss SNV dbSNP153 33..33 33 - - - 93485 RMVar_ID_93485 Human_SNP_ID_33347846 m1A Human chr1 - 150220150 150220149 150220150 TTGTCACAAGTAACTTGGAAAATAGAAGCAGAATAGTAAAGGTTCTATTCAGCAACATAGTTCAT TTGTCACAAGTAACTTGGAAAATAGAAGCAGA_TAGTAAAGGTTCTATTCAGCAACATAGTTCAT AT A ANP32E Ensembl:ENSG00000143401 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1412808242 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_325314,Human_RBP_ID_2092722,Human_RBP_ID_5136340,Human_RBP_ID_5686119,Human_RBP_ID_10567432,Human_RBP_ID_23330682,Human_RBP_ID_24398804,Human_RBP_ID_24447060,Human_RBP_ID_26367764,Human_RBP_ID_26840866 93486 RMVar_ID_93486 Human_SNP_ID_33347847 m1A Human chr1 - 150220150 150220150 150220150 TTGTCACAAGTAACTTGGAAAATAGAAGCAGAATAGTAAAGGTTCTATTCAGCAACATAGTTCAT TTGTCACAAGTAACTTGGAAAATAGAAGCAGAGTAGTAAAGGTTCTATTCAGCAACATAGTTCAT T C ANP32E Ensembl:ENSG00000143401 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6679147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325314,Human_RBP_ID_2092722,Human_RBP_ID_5136340,Human_RBP_ID_5686119,Human_RBP_ID_10567432,Human_RBP_ID_23330682,Human_RBP_ID_24398804,Human_RBP_ID_24447060,Human_RBP_ID_26367764,Human_RBP_ID_26840866 GWAS_ID_12192,GWAS_ID_12193 93487 RMVar_ID_93487 Human_SNP_ID_33347979 m1A Human chr1 + 150220689 150220689 150220689 CCAGAAACATTAGAGAATCTGGTCTTAGAATGATCTAGTCATCTTCTTCCTCTCCATCGTCTTCA CCAGAAACATTAGAGAATCTGGTCTTAGAATGGTCTAGTCATCTTCTTCCTCTCCATCGTCTTCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150220638..150230676 32194978 MeRIP-seq:(Medium) rs1320489974 Functional Loss SNV dbSNP153 33..33 33 - - - 93488 RMVar_ID_93488 Human_SNP_ID_33349703 m1A Human chr1 - 150226768 150226768 150226768 TAAAGATGGCGATGAAGATGATGAAGAGGAAGAGGAAAATGAAGCTGGTCCACCGGAAGGATATG TAAAGATGGCGATGAAGATGATGAAGAGGAAGGGGAAAATGAAGCTGGTCCACCGGAAGGATATG T C ANP32E Ensembl:ENSG00000143401 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr1:150226559..150229170;chr1:150226564..150229125 26863196 MeRIP-seq:(Medium) rs782722374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21087,Human_RBP_ID_1438200,Human_RBP_ID_2092760,Human_RBP_ID_3991447,Human_RBP_ID_5686206,Human_RBP_ID_9342224,Human_RBP_ID_18522562,Human_RBP_ID_22870937,Human_RBP_ID_23112453,Human_RBP_ID_23117568,Human_RBP_ID_24541209,Human_RBP_ID_26311739 Human_Splice_Rec_125922,Human_Splice_Rec_125930,Human_Splice_Rec_125942,Human_Splice_Rec_125952,Human_Splice_Rec_125974,Human_Splice_Rec_125984,Human_Splice_Rec_125990 Human_miRNA_ID_1781933 RMVar_hsa_circ_51775,RMVar_hsa_circ_307489,RMVar_hsa_circ_368933,RMVar_hsa_circ_365719,RMVar_hsa_circ_66515 93489 RMVar_ID_93489 Human_SNP_ID_33350950 m1A Human chr1 - 150231889 150231889 150231889 AGAGTTAGTCCTTGATAATTGCCTGTGTGTCAATGGGGAAATTGAAGGCCTGAATGATACTTTCA AGAGTTAGTCCTTGATAATTGCCTGTGTGTCAGTGGGGAAATTGAAGGCCTGAATGATACTTTCA T C ANP32E Ensembl:ENSG00000143401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150231838..150231984 26863196 MeRIP-seq:(Medium) rs782794752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21092,Human_RBP_ID_325354,Human_RBP_ID_1411217,Human_RBP_ID_1724905,Human_RBP_ID_2092770,Human_RBP_ID_3991462,Human_RBP_ID_5458344,Human_RBP_ID_8940013,Human_RBP_ID_8955699,Human_RBP_ID_9356775,Human_RBP_ID_17204280,Human_RBP_ID_18550857,Human_RBP_ID_23330731,Human_RBP_ID_26311743,Human_RBP_ID_27798478 Human_Splice_Rec_125916,Human_Splice_Rec_125936,Human_Splice_Rec_125948,Human_Splice_Rec_125962,Human_Splice_Rec_125980 Human_miRNA_ID_1180931,Human_miRNA_ID_1965171,Human_miRNA_ID_2360624,Human_miRNA_ID_2782022,Human_miRNA_ID_2784990 RMVar_hsa_circ_66515,RMVar_hsa_circ_349491,RMVar_hsa_circ_276670 93490 RMVar_ID_93490 Human_SNP_ID_33352032 m1A Human chr1 + 150236054 150236042 150236054 ACACACACGCACGCACGCGCGCACACACATACACACACACATACACACACACACCCGCAGTTCCT ACACACACGCACGCACGCGCG____________CACACACATACACACACACACCCGCAGTTCCT GCACACACATACA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150235697..150236150 26863196 MeRIP-seq:(Medium) rs60015667 Functional Loss DEL dbSNP153 22..33 33 - - - 93491 RMVar_ID_93491 Human_SNP_ID_33352038 m1A Human chr1 + 150236052 150236051 150236053 GCACACACACGCACGCACGCGCGCACACACATACACACACACATACACACACACACCCGCAGTTC GCACACACACGCACGCACGCGCGCACACACAT__ACACACACATACACACACACACCCGCAGTTC TAC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:150235958..150236132 26863196 MeRIP-seq:(Medium) rs1159794096 Functional Loss DEL dbSNP153 33..34 33 - - - 93492 RMVar_ID_93492 Human_SNP_ID_33352041 m1A Human chr1 + 150236052 150236052 150236052 GCACACACACGCACGCACGCGCGCACACACATACACACACACATACACACACACACCCGCAGTTC GCACACACACGCACGCACGCGCGCACACACATGCACACACACATACACACACACACCCGCAGTTC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:150235958..150236132 26863196 MeRIP-seq:(Medium) rs764904067 Functional Loss SNV dbSNP153 33..33 33 - - - 93493 RMVar_ID_93493 Human_SNP_ID_33352044 m1A Human chr1 + 150236054 150236054 150236054 ACACACACGCACGCACGCGCGCACACACATACACACACACATACACACACACACCCGCAGTTCCT ACACACACGCACGCACGCGCGCACACACATACTCACACACATACACACACACACCCGCAGTTCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150235697..150236150 26863196 MeRIP-seq:(Medium) rs587684856 Functional Loss SNV dbSNP153 33..33 33 - - - 93494 RMVar_ID_93494 Human_SNP_ID_33359946 m1A Human chr1 + 150265798 150265797 150265798 GAGCCCAGCCATGAGGAGCAACTCGAGGAGAGAAAATATAGCCCAAGGAGGTTAGAAGAGTTCCA GAGCCCAGCCATGAGGAGCAACTCGAGGAGAG_AAATATAGCCCAAGGAGGTTAGAAGAGTTCCA GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:150265751..150265925 26863196 MeRIP-seq:(Medium) rs1188518121 Functional Loss DEL dbSNP153 33..33 33 - - - 93495 RMVar_ID_93495 Human_SNP_ID_33359991 m1A Human chr1 + 150265973 150265973 150265973 GTCTTGAGGGAGTACTGAGAAACTCAGAGCTCATCTATCCTTGAGCCTCCATTAATTTCATCTCC GTCTTGAGGGAGTACTGAGAAACTCAGAGCTCGTCTATCCTTGAGCCTCCATTAATTTCATCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150265922..150266084 26863196 MeRIP-seq:(Medium) rs1218538267 Functional Loss SNV dbSNP153 33..33 33 - - - 93496 RMVar_ID_93496 Human_SNP_ID_33360039 m1A Human chr1 - 150266134 150266134 150266134 GGTGTATTCTGCCCTGCGCATCCCACCCGAGGACTGAGGGAACCTAGGGGGGACCCCTGGGCCTG GGTGTATTCTGCCCTGCGCATCCCACCCGAGGGCTGAGGGAACCTAGGGGGGACCCCTGGGCCTG T C APH1A Ensembl:ENSG00000117362 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:150266084..150266450 26863196 MeRIP-seq:(Medium) rs1553849757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325408,Human_RBP_ID_3991521,Human_RBP_ID_5484278,Human_RBP_ID_8169581,Human_RBP_ID_10567794,Human_RBP_ID_17338385,Human_RBP_ID_17647049,Human_RBP_ID_17724901,Human_RBP_ID_22779798,Human_RBP_ID_27167481,Human_RBP_ID_27387623 Human_Splice_Rec_126084,Human_Splice_Rec_126096 Human_miRNA_ID_1327903 93497 RMVar_ID_93497 Human_SNP_ID_33360161 m1A Human chr1 - 150266492 150266492 150266492 TGACTACCTGGACTGATCGCCTGACAGATCCCACCTGCCTGTCCACTGCCCATGACTGAGCCCAG TGACTACCTGGACTGATCGCCTGACAGATCCCCCCTGCCTGTCCACTGCCCATGACTGAGCCCAG T G APH1A Ensembl:ENSG00000117362 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150266454..150266550 26863196 MeRIP-seq:(Medium) rs201680381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325426,Human_RBP_ID_5686315,Human_RBP_ID_8284519,Human_RBP_ID_10567821,Human_RBP_ID_17212129,Human_RBP_ID_19039041,Human_RBP_ID_19187238,Human_RBP_ID_23330795,Human_RBP_ID_26798812,Human_RBP_ID_27167488 Human_miRNA_ID_1700575 93498 RMVar_ID_93498 Human_SNP_ID_33360171 m1A Human chr1 + 150266508 150266508 150266508 GCAGTGGACAGGCAGGTGGGATCTGTCAGGCGATCAGTCCAGGTAGTCAGTCCTTACACAAGAGG GCAGTGGACAGGCAGGTGGGATCTGTCAGGCGTTCAGTCCAGGTAGTCAGTCCTTACACAAGAGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150266468..150266564 26863196 MeRIP-seq:(Medium) rs1202236644 Functional Loss SNV dbSNP153 33..33 33 - - - 93499 RMVar_ID_93499 Human_SNP_ID_33360390 m1A Human chr1 + 150267360 150267360 150267360 TAAAGGCTAGATAGAAGGTGGATCTTACCTGAAGTCAGGAAGTAATAGGGTGAGTCTCCATGGAT TAAAGGCTAGATAGAAGGTGGATCTTACCTGAGGTCAGGAAGTAATAGGGTGAGTCTCCATGGAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150267351..150267500 32194978 MeRIP-seq:(Medium) rs1553850139 Functional Loss SNV dbSNP153 33..33 33 - - - 93500 RMVar_ID_93500 Human_SNP_ID_33360809 m1A Human chr1 - 150268834 150268833 150268834 CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCCACCCCCCTTCCCACCTGACCAGCCATGGGGGCT CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCC_CCCCCCTTCCCACCTGACCAGCCATGGGGGCT GT G APH1A Ensembl:ENSG00000117362 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr1:150268630..150268952;chr1:150268788..150268945 26863196 MeRIP-seq:(Medium) rs1560036083 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_325451,Human_RBP_ID_3991587,Human_RBP_ID_5432851,Human_RBP_ID_5456261,Human_RBP_ID_9320150,Human_RBP_ID_18187250,Human_RBP_ID_27835281 93501 RMVar_ID_93501 Human_SNP_ID_33360811 m1A Human chr1 - 150268834 150268834 150268834 CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCCACCCCCCTTCCCACCTGACCAGCCATGGGGGCT CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCCTCCCCCCTTCCCACCTGACCAGCCATGGGGGCT T A APH1A Ensembl:ENSG00000117362 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr1:150268630..150268952;chr1:150268788..150268945 26863196 MeRIP-seq:(Medium) rs781967022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325451,Human_RBP_ID_3991587,Human_RBP_ID_5432851,Human_RBP_ID_5456261,Human_RBP_ID_9320150,Human_RBP_ID_18187250,Human_RBP_ID_27835281 93502 RMVar_ID_93502 Human_SNP_ID_33360812 m1A Human chr1 - 150268834 150268834 150268834 CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCCACCCCCCTTCCCACCTGACCAGCCATGGGGGCT CCCTCCCATTTGCCTGTCCTGGTCAGGCCCCCCCCCCCCTTCCCACCTGACCAGCCATGGGGGCT T G APH1A Ensembl:ENSG00000117362 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr1:150268630..150268952;chr1:150268788..150268945 26863196 MeRIP-seq:(Medium) rs781967022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325451,Human_RBP_ID_3991587,Human_RBP_ID_5432851,Human_RBP_ID_5456261,Human_RBP_ID_9320150,Human_RBP_ID_18187250,Human_RBP_ID_27835281 93503 RMVar_ID_93503 Human_SNP_ID_33360829 m1A Human chr1 - 150268884 150268884 150268884 CCCTCGTGGGGTCGCGTTGCCACCCCACGCGGACTCCCCAGCTGGCGCGCCCCTCCCATTTGCCT CCCTCGTGGGGTCGCGTTGCCACCCCACGCGGTCTCCCCAGCTGGCGCGCCCCTCCCATTTGCCT T A APH1A Ensembl:ENSG00000117362 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:150268842..150269000 26863196 MeRIP-seq:(Medium) rs200412198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325453,Human_RBP_ID_3991588,Human_RBP_ID_5484282,Human_RBP_ID_8734480,Human_RBP_ID_9319120,Human_RBP_ID_10567882,Human_RBP_ID_26840925,Human_RBP_ID_27167503 93504 RMVar_ID_93504 Human_SNP_ID_33364297 m1A Human chr1 + 150282665 150282665 150282665 AGGACAAAGCGAGCTGTTAGGGAGTATTTGGGAGTGGATTTGGGGGCTGAATGCAGATCTTGGTA AGGACAAAGCGAGCTGTTAGGGAGTATTTGGGGGTGGATTTGGGGGCTGAATGCAGATCTTGGTA A G CIART Ensembl:ENSG00000159208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150282662..150282753 26863196 MeRIP-seq:(Medium) rs944442795 Functional Loss SNV dbSNP153 33..33 33 - - - 93505 RMVar_ID_93505 Human_SNP_ID_33367300 m1A Human chr1 - 150293900 150293895 150293900 CCTTCCTTTCCCCAAACCCTGCACAACTCCTCACCTCGCGCGCTCAGTACCTAGCCCACCGGAAG CCTTCCTTTCCCCAAACCCTGCACAACTCCTC_____GCGCGCTCAGTACCTAGCCCACCGGAAG CGAGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:150293851..150294000;chr1:150293851..150294059;chr1:150293851..150294016;chr1:150293851..150294003 26863196 MeRIP-seq:(Medium) rs1461597281 Functional Loss DEL dbSNP153 33..37 33 - - - 93506 RMVar_ID_93506 Human_SNP_ID_33371274 m1A Human chr1 + 150308010 150308010 150308010 TCTATTTATGAAACTGGAAAAGAATAATGATGATCCCAAATGTCTAACCTCATTGCTTGCCTTTA TCTATTTATGAAACTGGAAAAGAATAATGATGTTCCCAAATGTCTAACCTCATTGCTTGCCTTTA A T MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150308007..150308289 26863196 MeRIP-seq:(Medium) rs782050845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8284549,Human_RBP_ID_24583953 93507 RMVar_ID_93507 Human_SNP_ID_33371275 m1A Human chr1 - 150308011 150308011 150308011 ATAAAGGCAAGCAATGAGGTTAGACATTTGGGATCATCATTATTCTTTTCCAGTTTCATAAATAG ATAAAGGCAAGCAATGAGGTTAGACATTTGGGGTCATCATTATTCTTTTCCAGTTTCATAAATAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150308007..150308163 26863196 MeRIP-seq:(Medium) rs1553858786 Functional Loss SNV dbSNP153 33..33 33 - - - 93508 RMVar_ID_93508 Human_SNP_ID_33371288 m1A Human chr1 + 150308029 150308029 150308029 AAGAATAATGATGATCCCAAATGTCTAACCTCATTGCTTGCCTTTATACAGAATCCTCACTATGG AAGAATAATGATGATCCCAAATGTCTAACCTCGTTGCTTGCCTTTATACAGAATCCTCACTATGG A G MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150308026..150308050 32194978 MeRIP-seq:(Medium) rs200920233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24583953 93509 RMVar_ID_93509 Human_SNP_ID_33371339 m1A Human chr1 + 150308151 150308151 150308151 GACAGAGGGAAAGCTATGAAAGGTGCCGGCGGATCTACAACATGGAAATGGCTCGCAAGATCAAC GACAGAGGGAAAGCTATGAAAGGTGCCGGCGGGTCTACAACATGGAAATGGCTCGCAAGATCAAC A G MRPS21 Ensembl:ENSG00000266472 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:150308126..150308150 26863196 MeRIP-seq:(Medium) rs782681271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325471,Human_RBP_ID_970948,Human_RBP_ID_5686387,Human_RBP_ID_9356782,Human_RBP_ID_10568189,Human_RBP_ID_17724923,Human_RBP_ID_18428489,Human_RBP_ID_22127117,Human_RBP_ID_22485814,Human_RBP_ID_22564040,Human_RBP_ID_23121375,Human_RBP_ID_23330854,Human_RBP_ID_27387651 93510 RMVar_ID_93510 Human_SNP_ID_33371376 m1A Human chr1 + 150308243 150308243 150308243 CCGTGGCAGGGCTGCTGAGGCCTGTGGGTGGGACACCCAGTGCGAAACCCTCATCCAGTTTTCTC CCGTGGCAGGGCTGCTGAGGCCTGTGGGTGGGGCACCCAGTGCGAAACCCTCATCCAGTTTTCTC A G MRPS21 Ensembl:ENSG00000266472 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150294326..150308375 32194978 MeRIP-seq:(Medium) rs1480595405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325473,Human_RBP_ID_4080857,Human_RBP_ID_5686388,Human_RBP_ID_8284552,Human_RBP_ID_8955733,Human_RBP_ID_10568193,Human_RBP_ID_17647640,Human_RBP_ID_17724924,Human_RBP_ID_22023747,Human_RBP_ID_22427476,Human_RBP_ID_27167518 93511 RMVar_ID_93511 Human_SNP_ID_33374963 m1A Human chr1 - 150321594 150321594 150321594 AATTACCCTCTGTGGGCCCGGGGCCACTACTCACCTCACAAACTTCAGCCCCTGAGACGGAGCCC AATTACCCTCTGTGGGCCCGGGGCCACTACTCGCCTCACAAACTTCAGCCCCTGAGACGGAGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:150321587..150321698;chr1:150321475..150322033;chr1:150321480..150322034;chr1:150321494..150321938 26863196 MeRIP-seq:(Medium) rs1438777644 Functional Loss SNV dbSNP153 33..33 33 - - - 93512 RMVar_ID_93512 Human_SNP_ID_33376584 m1A Human chr1 + 150328020 150328019 150328020 GGAGGAGGTGAGTTTTAGGCAGGATTTGGAACAGGGGTTGTGGAAAAGTTGAGAGAAATCATTAT GGAGGAGGTGAGTTTTAGGCAGGATTTGGAAC_GGGGTTGTGGAAAAGTTGAGAGAAATCATTAT CA C PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150328015..150328080 26863196 MeRIP-seq:(Medium) rs1336203656 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10568530 RMVar_hsa_circ_310454,RMVar_hsa_circ_355159,RMVar_hsa_circ_319565,RMVar_hsa_circ_19437,RMVar_hsa_circ_351891,RMVar_hsa_circ_352571,RMVar_hsa_circ_362153,RMVar_hsa_circ_277133,RMVar_hsa_circ_135873 93513 RMVar_ID_93513 Human_SNP_ID_33386503 m1A Human chr1 + 150364253 150364253 150364253 TAGCGAGTCTAAAGGAAAGAAAGATTTCTGCAACTGAAGGGGCAGTCGGGTAGTATTACATTTAA TAGCGAGTCTAAAGGAAAGAAAGATTTCTGCAGCTGAAGGGGCAGTCGGGTAGTATTACATTTAA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150364202..150364338 26863196 MeRIP-seq:(Medium) rs1553876687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1724991,Human_RBP_ID_4076975,Human_RBP_ID_10569431,Human_RBP_ID_18415052 93514 RMVar_ID_93514 Human_SNP_ID_33392356 m1A Human chr1 - 150385979 150385979 150385979 CACTTTCAATACAAACTCTACCCTACTTACCTACGATTTATTACTCAACTCAGGAAACTCCCCTA CACTTTCAATACAAACTCTACCCTACTTACCTGCGATTTATTACTCAACTCAGGAAACTCCCCTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150385977..150386058 26863196 MeRIP-seq:(Medium) rs1369451528 Functional Loss SNV dbSNP153 33..33 33 - - - 93515 RMVar_ID_93515 Human_SNP_ID_33414461 m1A Human chr1 + 150472250 150472250 150472250 TCACAGTGCATCCAATAGGAGGATGTCAGGGGAGCCGATCCAGACCGTAGAGTCCATCCGAGTTC TCACAGTGCATCCAATAGGAGGATGTCAGGGGTGCCGATCCAGACCGTAGAGTCCATCCGAGTTC A T RPRD2 Ensembl:ENSG00000163125 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150472201..150472394 26863196 MeRIP-seq:(Medium) rs1156611385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2093074,Human_RBP_ID_5686950,Human_RBP_ID_22023760 93516 RMVar_ID_93516 Human_SNP_ID_33418711 m1A Human chr1 + 150487860 150487860 150487860 TGTTACCTGCTAATATATCTTTCCCTCCAGGCAGTTGTGTCGACCCCTCCACGCTGGTTGGCAGA TGTTACCTGCTAATATATCTTTCCCTCCAGGCCGTTGTGTCGACCCCTCCACGCTGGTTGGCAGA A C TARS2 Ensembl:ENSG00000143374 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150487851..150487925 32194978 MeRIP-seq:(Medium) rs772482080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3991836 Human_Splice_Rec_126374,Human_Splice_Rec_126398,Human_Splice_Rec_126424,Human_Splice_Rec_126458,Human_Splice_Rec_126488,Human_Splice_Rec_126492,Human_Splice_Rec_126516 RMVar_hsa_circ_9525,RMVar_hsa_circ_61140,RMVar_hsa_circ_94626,RMVar_hsa_circ_135901,RMVar_hsa_circ_135902,RMVar_hsa_circ_34053 93517 RMVar_ID_93517 Human_SNP_ID_33425301 m1A Human chr1 + 150510961 150510961 150510961 GCAGCCCAGCACTGCCAACAGGACCGGTCCCAAGGGGGCTGGGGCCACCGGCTGGATGGCTTCCC GCAGCCCAGCACTGCCAACAGGACCGGTCCCAGGGGGGCTGGGGCCACCGGCTGGATGGCTTCCC A G ECM1 Ensembl:ENSG00000143369 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150510914..150511013 32194978 MeRIP-seq:(Medium) rs768806152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22749416 Human_Splice_Rec_126608,Human_Splice_Rec_126624,Human_Splice_Rec_126640,Human_Splice_Rec_126656 RMVar_hsa_circ_128202,RMVar_hsa_circ_135913 93518 RMVar_ID_93518 Human_SNP_ID_33425631 m1A Human chr1 + 150511749 150511749 150511749 CAACCTGCCAGCTACTGACCCCCTACAAAGGGAGCTGCTGGCACTGATCCAGCTGGAGAGGGAGT CAACCTGCCAGCTACTGACCCCCTACAAAGGGTGCTGCTGGCACTGATCCAGCTGGAGAGGGAGT A T ECM1 Ensembl:ENSG00000143369 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150511605..150512472 32194978 MeRIP-seq:(Medium) rs587775247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22749420 Human_Splice_Rec_126593,Human_Splice_Rec_126611,Human_Splice_Rec_126659 Human_miRNA_ID_1999321,Human_miRNA_ID_2192037,Human_miRNA_ID_2206246,Human_miRNA_ID_2767910 RMVar_hsa_circ_128202,RMVar_hsa_circ_135913 93519 RMVar_ID_93519 Human_SNP_ID_33436044 m1A Human chr1 - 150549878 150549878 150549878 ATCAAGGGCACCCACCTGCGTCCCTCGCGGCGACCCTGTCCTCCAAGTTCAGGAGTGCAGTGGGG ATCAAGGGCACCCACCTGCGTCCCTCGCGGCGCCCCTGTCCTCCAAGTTCAGGAGTGCAGTGGGG T G ADAMTSL4-AS2 Ensembl:ENSG00000237781 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:150549767..150549972;chr1:150549799..150549950 26863196 MeRIP-seq:(Medium) rs587771487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241687 93520 RMVar_ID_93520 Human_SNP_ID_33437097 m1A Human chr1 + 150553503 150553503 150553503 GAGAGTGCCCTTTGCATTGCCACTGCACCGGAACCGCAGGCACCCTCGGAGCCCACCCAGATCTG GAGAGTGCCCTTTGCATTGCCACTGCACCGGACCCGCAGGCACCCTCGGAGCCCACCCAGATCTG A C ADAMTSL4 Ensembl:ENSG00000143382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150553454..150553605 32194978 MeRIP-seq:(Medium) rs373098149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741365,Human_RBP_ID_3933925,Human_RBP_ID_17071952,Human_RBP_ID_22023771 Human_Splice_Rec_126692,Human_Splice_Rec_126730,Human_Splice_Rec_126766,Human_Splice_Rec_126796,Human_Splice_Rec_126832,Human_Splice_Rec_126866 RMVar_hsa_circ_378875,RMVar_hsa_circ_45523,RMVar_hsa_circ_79678,RMVar_hsa_circ_135916,RMVar_hsa_circ_82583,RMVar_hsa_circ_135917 93521 RMVar_ID_93521 Human_SNP_ID_33438748 m1A Human chr1 + 150557548 150557548 150557548 CTGCATCTCCCGTGAGTCGGGAGAGGAACTGGATGAACGCAGCTGTGCCGCGGGTGCCAGGCCCC CTGCATCTCCCGTGAGTCGGGAGAGGAACTGGCTGAACGCAGCTGTGCCGCGGGTGCCAGGCCCC A C ADAMTSL4 Ensembl:ENSG00000143382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150555486..150557724 32194978 MeRIP-seq:(Medium) rs777396369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3936560,Human_RBP_ID_22025306 Human_Splice_Rec_126708,Human_Splice_Rec_126709,Human_Splice_Rec_126744,Human_Splice_Rec_126745,Human_Splice_Rec_126780,Human_Splice_Rec_126781,Human_Splice_Rec_126812,Human_Splice_Rec_126813,Human_Splice_Rec_126848,Human_Splice_Rec_126849,Human_Splice_Rec_126880,Human_Splice_Rec_126881 RMVar_hsa_circ_79678,RMVar_hsa_circ_135916,RMVar_hsa_circ_82583,RMVar_hsa_circ_135917 93522 RMVar_ID_93522 Human_SNP_ID_33438749 m1A Human chr1 + 150557548 150557548 150557548 CTGCATCTCCCGTGAGTCGGGAGAGGAACTGGATGAACGCAGCTGTGCCGCGGGTGCCAGGCCCC CTGCATCTCCCGTGAGTCGGGAGAGGAACTGGGTGAACGCAGCTGTGCCGCGGGTGCCAGGCCCC A G ADAMTSL4 Ensembl:ENSG00000143382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150555486..150557724 32194978 MeRIP-seq:(Medium) rs777396369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3936560,Human_RBP_ID_22025306 Human_Splice_Rec_126708,Human_Splice_Rec_126709,Human_Splice_Rec_126744,Human_Splice_Rec_126745,Human_Splice_Rec_126780,Human_Splice_Rec_126781,Human_Splice_Rec_126812,Human_Splice_Rec_126813,Human_Splice_Rec_126848,Human_Splice_Rec_126849,Human_Splice_Rec_126880,Human_Splice_Rec_126881 RMVar_hsa_circ_79678,RMVar_hsa_circ_135916,RMVar_hsa_circ_82583,RMVar_hsa_circ_135917 93523 RMVar_ID_93523 Human_SNP_ID_33443886 m1A Human chr1 + 150574856 150574855 150574856 ATCCTCCCTTTCCCTTTTGGAGGATTTGCCCGAACTACGTAGCCAGTCAGCACTTAGACCACCTG ATCCTCCCTTTCCCTTTTGGAGGATTTGCCCG_ACTACGTAGCCAGTCAGCACTTAGACCACCTG GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150574805..150575031 26863196 MeRIP-seq:(Medium) rs1176054465 Functional Loss DEL dbSNP153 33..33 33 - - - 93524 RMVar_ID_93524 Human_SNP_ID_33443918 m1A Human chr1 + 150574969 150574969 150574969 CCACTTGGGGTGTCCTAAGCCCTCACTGCCCCAAGCCCAAAATATCAACTAAGATCCTTGTCTGT CCACTTGGGGTGTCCTAAGCCCTCACTGCCCCGAGCCCAAAATATCAACTAAGATCCTTGTCTGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150574805..150575007 26863196 MeRIP-seq:(Medium) rs1189052601 Functional Loss SNV dbSNP153 33..33 33 - - - 93525 RMVar_ID_93525 Human_SNP_ID_33444220 m1A Human chr1 - 150576091 150576091 150576091 GATGGAGAGACATTTGATCCCTTGTTTGCTTAATAAATTATAAAATGATGGCTTGGAAAAGCAGG GATGGAGAGACATTTGATCCCTTGTTTGCTTACTAAATTATAAAATGATGGCTTGGAAAAGCAGG T G MCL1 Ensembl:ENSG00000143384 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150575990..150576090 32194978 MeRIP-seq:(Medium) rs748026354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_971011,Human_RBP_ID_1725083,Human_RBP_ID_3280814,Human_RBP_ID_5687318,Human_RBP_ID_8284784,Human_RBP_ID_8734610,Human_RBP_ID_17445920,Human_RBP_ID_17725128,Human_RBP_ID_18216710,Human_RBP_ID_22373416,Human_RBP_ID_22846604,Human_RBP_ID_23331301,Human_RBP_ID_24447138,Human_RBP_ID_24751658,Human_RBP_ID_26578102,Human_RBP_ID_27167641,Human_RBP_ID_27578633 RMVar_hsa_circ_75621,RMVar_hsa_circ_81857,RMVar_hsa_circ_135919,RMVar_hsa_circ_135920 93526 RMVar_ID_93526 Human_SNP_ID_33444902 m1A Human chr1 - 150578305 150578305 150578305 AAACCAAGAAAGCTGCATCGAACCATTAGCAGAAAGTATCACAGACGTTCTCGTAAGGACAAAAC AAACCAAGAAAGCTGCATCGAACCATTAGCAGTAAGTATCACAGACGTTCTCGTAAGGACAAAAC T A MCL1 Ensembl:ENSG00000143384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:150578254..150578334 26863196 MeRIP-seq:(Medium) rs921336171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1411461,Human_RBP_ID_1725109,Human_RBP_ID_2093256,Human_RBP_ID_5536472,Human_RBP_ID_5687402,Human_RBP_ID_8734640,Human_RBP_ID_10571971,Human_RBP_ID_18551073,Human_RBP_ID_22127274,Human_RBP_ID_22846637,Human_RBP_ID_27167664 Human_Splice_Rec_126907,Human_Splice_Rec_126911,Human_Splice_Rec_126913 RMVar_hsa_circ_75621,RMVar_hsa_circ_81857,RMVar_hsa_circ_114084,RMVar_hsa_circ_135919,RMVar_hsa_circ_135920,RMVar_hsa_circ_135923 93527 RMVar_ID_93527 Human_SNP_ID_33444967 m1A Human chr1 - 150578489 150578489 150578489 CGTGAGGACCTGCATGCTTTTCTTTCTCAGGCATGCTTCGGAAACTGGACATCAAAAACGAAGAC CGTGAGGACCTGCATGCTTTTCTTTCTCAGGCCTGCTTCGGAAACTGGACATCAAAAACGAAGAC T G MCL1 Ensembl:ENSG00000143384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:150578411..150578524;chr1:150578401..150578531;chr1:150578451..150578525;chr1:150578401..150578625;chr1:150578431..150578531;chr1:150578325..150578531;chr1:150578394..150578500 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs140449444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_852874,Human_RBP_ID_1411466,Human_RBP_ID_1725111,Human_RBP_ID_3933945,Human_RBP_ID_3992077,Human_RBP_ID_5687407,Human_RBP_ID_8284808,Human_RBP_ID_8734645,Human_RBP_ID_10571982,Human_RBP_ID_22560163,Human_RBP_ID_27167668 Human_Splice_Rec_126906,Human_Splice_Rec_126910 Human_miRNA_ID_2069238,Human_miRNA_ID_2802136 RMVar_hsa_circ_75621,RMVar_hsa_circ_81857,RMVar_hsa_circ_114084,RMVar_hsa_circ_135919,RMVar_hsa_circ_135920,RMVar_hsa_circ_135923 93528 RMVar_ID_93528 Human_SNP_ID_33445166 m1A Human chr1 - 150578960 150578960 150578960 AGATTATCTCTCGGTACCTTCGGGAGCAGGCCACCGGCGCCAAGGACACAAAGCCAATGGGCAGG AGATTATCTCTCGGTACCTTCGGGAGCAGGCCGCCGGCGCCAAGGACACAAAGCCAATGGGCAGG T C MCL1 Ensembl:ENSG00000143384 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150578843..150579550 32194978 MeRIP-seq:(Medium) rs764147144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4080966,Human_RBP_ID_5687415,Human_RBP_ID_8755112,Human_RBP_ID_9270318,Human_RBP_ID_17725153,Human_RBP_ID_18551079,Human_RBP_ID_22015713,Human_RBP_ID_23117671,Human_RBP_ID_26311775,Human_RBP_ID_27167672,Human_RBP_ID_27387835 Human_miRNA_ID_2216696,Human_miRNA_ID_2929470 RMVar_hsa_circ_75621,RMVar_hsa_circ_135920,RMVar_hsa_circ_269447 93529 RMVar_ID_93529 Human_SNP_ID_33445188 m1A Human chr1 - 150578992 150578992 150578992 GGAGGAGGACGAGTTGTACCGGCAGTCGCTGGAGATTATCTCTCGGTACCTTCGGGAGCAGGCCA GGAGGAGGACGAGTTGTACCGGCAGTCGCTGGGGATTATCTCTCGGTACCTTCGGGAGCAGGCCA T C MCL1 Ensembl:ENSG00000143384 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150578942..150579192 32194978 MeRIP-seq:(Medium) rs748809663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8734654,Human_RBP_ID_9270319,Human_RBP_ID_10571990,Human_RBP_ID_17725153,Human_RBP_ID_22023785 RMVar_hsa_circ_75621,RMVar_hsa_circ_135920 93530 RMVar_ID_93530 Human_SNP_ID_33445328 m1A Human chr1 + 150579236 150579233 150579236 CTCAAGCGGCGCCGCGCGGCGGGTGGGCGCGAAGAAAAGCAGCCTCGCGGGGGTCGCGGTGACGT CTCAAGCGGCGCCGCGCGGCGGGTGGGCGC___GAAAAGCAGCCTCGCGGGGGTCGCGGTGACGT CGAA C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:150578752..150579600;chr1:150578726..150579600 26863196 MeRIP-seq:(Medium) rs764173760 Functional Loss DEL dbSNP153 31..33 33 - - - 93531 RMVar_ID_93531 Human_SNP_ID_33445441 m1A Human chr1 - 150579419 150579419 150579419 GCGCCACCCGCCCGGGAGGGCGACTTTTGGCTACGGAGAAGGAGGCCTCGGCCCGGCGAGAGATA GCGCCACCCGCCCGGGAGGGCGACTTTTGGCTTCGGAGAAGGAGGCCTCGGCCCGGCGAGAGATA T A MCL1 Ensembl:ENSG00000143384 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:150578768..150579575 26863196 MeRIP-seq:(Medium) rs768191690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804521,Human_RBP_ID_4080979,Human_RBP_ID_5687419,Human_RBP_ID_9320160,Human_RBP_ID_22023793,Human_RBP_ID_22428572,Human_RBP_ID_24584860 Human_miRNA_ID_1342154,Human_miRNA_ID_2667464 RMVar_hsa_circ_75621,RMVar_hsa_circ_135920 93532 RMVar_ID_93532 Human_SNP_ID_33456796 m1A Human chr1 + 150622851 150622851 150622851 GGATCTGGCAGAGCCCCGGGCAGCATCATTCAACTTGGCCACTGCGGACGAACACAGAAGAAAAA GGATCTGGCAGAGCCCCGGGCAGCATCATTCACCTTGGCCACTGCGGACGAACACAGAAGAAAAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150622801..150622875 26863196 MeRIP-seq:(Medium) rs587672876 Functional Loss SNV dbSNP153 33..33 33 - - - 93533 RMVar_ID_93533 Human_SNP_ID_33456799 m1A Human chr1 + 150622859 150622859 150622859 CAGAGCCCCGGGCAGCATCATTCAACTTGGCCACTGCGGACGAACACAGAAGAAAAAAAAAAAAA CAGAGCCCCGGGCAGCATCATTCAACTTGGCCCCTGCGGACGAACACAGAAGAAAAAAAAAAAAA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150622818..150623340 26863196 MeRIP-seq:(Medium) rs1269588765 Functional Loss SNV dbSNP153 33..33 33 - - - 93534 RMVar_ID_93534 Human_SNP_ID_33457993 m1A Human chr1 - 150627576 150627576 150627576 CATTTGTTTTCTCCAGGACACGCAGGAGAAAGAAGGTATTCTGCCTGAGAGAGCTGAAGAGGCAA CATTTGTTTTCTCCAGGACACGCAGGAGAAAGGAGGTATTCTGCCTGAGAGAGCTGAAGAGGCAA T C ENSA Ensembl:ENSG00000143420 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150627526..150627600 32194978 MeRIP-seq:(Medium) rs747403259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222211,Human_RBP_ID_271811,Human_RBP_ID_325754,Human_RBP_ID_804762,Human_RBP_ID_1411525,Human_RBP_ID_1725167,Human_RBP_ID_3933946,Human_RBP_ID_5109194,Human_RBP_ID_8170676,Human_RBP_ID_8955871,Human_RBP_ID_11183037,Human_RBP_ID_18415053,Human_RBP_ID_23426219,Human_RBP_ID_26311776 Human_Splice_Rec_126918,Human_Splice_Rec_126926,Human_Splice_Rec_126932,Human_Splice_Rec_126938,Human_Splice_Rec_126946,Human_Splice_Rec_126954,Human_Splice_Rec_126962,Human_Splice_Rec_126968,Human_Splice_Rec_126972,Human_Splice_Rec_126976,Human_Splice_Rec_126982,Human_Splice_Rec_126986,Human_Splice_Rec_126990,Human_Splice_Rec_126996 RMVar_hsa_circ_85281,RMVar_hsa_circ_350296,RMVar_hsa_circ_135925 93535 RMVar_ID_93535 Human_SNP_ID_33458340 m1A Human chr1 + 150629010 150629010 150629010 GTTTTTTTTTAAACGTCTTTACCTCGACCCCTATCTTTGCGGATTGAGGCTGCGGGCCCCAGCCC GTTTTTTTTTAAACGTCTTTACCTCGACCCCTGTCTTTGCGGATTGAGGCTGCGGGCCCCAGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150629008..150629150 26863196 MeRIP-seq:(Medium) rs754074553 Functional Loss SNV dbSNP153 33..33 33 - - - 93536 RMVar_ID_93536 Human_SNP_ID_33458341 m1A Human chr1 - 150629011 150629011 150629011 CGGGCTGGGGCCCGCAGCCTCAATCCGCAAAGATAGGGGTCGAGGTAAAGACGTTTAAAAAAAAA CGGGCTGGGGCCCGCAGCCTCAATCCGCAAAGGTAGGGGTCGAGGTAAAGACGTTTAAAAAAAAA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150629009..150629150 26863196 MeRIP-seq:(Medium) rs1208206931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_126985 RMVar_hsa_circ_85281,RMVar_hsa_circ_135925 93537 RMVar_ID_93537 Human_SNP_ID_33458576 m1A Human chr1 + 150629525 150629525 150629525 GTAAGGGGCCCGGGAAGGCAACCGGAGAAGGGAAGGGGGAGGGGAAACGGGGACAACCTGCGCTG GTAAGGGGCCCGGGAAGGCAACCGGAGAAGGGGAGGGGGAGGGGAAACGGGGACAACCTGCGCTG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:150629426..150629575 26863410 MeRIP-seq:(Medium) rs1016518214 Functional Loss SNV dbSNP153 33..33 33 - - - 93538 RMVar_ID_93538 Human_SNP_ID_33458585 m1A Human chr1 + 150629545 150629545 150629545 ACCGGAGAAGGGAAGGGGGAGGGGAAACGGGGACAACCTGCGCTGCTGCTTCGGCTCCTGTCACT ACCGGAGAAGGGAAGGGGGAGGGGAAACGGGGCCAACCTGCGCTGCTGCTTCGGCTCCTGTCACT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:150629401..150629600 26863196 MeRIP-seq:(Medium) rs1285566373 Functional Loss SNV dbSNP153 33..33 33 - - - 93539 RMVar_ID_93539 Human_SNP_ID_33458588 m1A Human chr1 - 150629556 150629556 150629556 TGAGCAACCCTAGTGACAGGAGCCGAAGCAGCAGCGCAGGTTGTCCCCGTTTCCCCTCCCCCTTC TGAGCAACCCTAGTGACAGGAGCCGAAGCAGCCGCGCAGGTTGTCCCCGTTTCCCCTCCCCCTTC T G ENSA Ensembl:ENSG00000143420 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:150629401..150629600 26863196 MeRIP-seq:(Medium) rs1000836365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325757,Human_RBP_ID_804716,Human_RBP_ID_3992306,Human_RBP_ID_8284870,Human_RBP_ID_17072458,Human_RBP_ID_18929944,Human_RBP_ID_22015736,Human_RBP_ID_22127324,Human_RBP_ID_26841192 Human_Splice_Rec_126979 RMVar_hsa_circ_85281,RMVar_hsa_circ_135925 93540 RMVar_ID_93540 Human_SNP_ID_33472839 m1A Human chr1 - 150690729 150690729 150690729 ATGGAGAAAAGGAAACACGTTCTGGATGAGGGAACCTGAGTGAGCAAAGGTATCATGAGCTTGAT ATGGAGAAAAGGAAACACGTTCTGGATGAGGGGACCTGAGTGAGCAAAGGTATCATGAGCTTGAT T C GOLPH3L Ensembl:ENSG00000143457 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150690714..150690812 26863196 MeRIP-seq:(Medium) rs1233784811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10573269,Human_RBP_ID_23331513 RMVar_hsa_circ_93444,RMVar_hsa_circ_135927,RMVar_hsa_circ_75597,RMVar_hsa_circ_135926,RMVar_hsa_circ_45177 93541 RMVar_ID_93541 Human_SNP_ID_33501362 m1A Human chr1 - 150811479 150811465 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGT______________GTGTGTGCGCACACATGCT CACACACACACACAT C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1321344117 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 93542 RMVar_ID_93542 Human_SNP_ID_33501366 m1A Human chr1 - 150811479 150811469 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGT__________GTGTGTGTGTGCGCACACATGCT CACACACACAT C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs967619713 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 93543 RMVar_ID_93543 Human_SNP_ID_33501371 m1A Human chr1 - 150811479 150811473 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGT______GTGTGTGTGTGTGTGCGCACACATGCT CACACAT C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs760531583 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 93544 RMVar_ID_93544 Human_SNP_ID_33501376 m1A Human chr1 - 150811479 150811475 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGT____GTGTGTGTGTGTGTGTGCGCACACATGCT CACAT C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1450820233 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 93545 RMVar_ID_93545 Human_SNP_ID_33501378 m1A Human chr1 - 150811479 150811479 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCACACATGCT T C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61817635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 93546 RMVar_ID_93546 Human_SNP_ID_33502620 m1A Human chr1 - 150816405 150816405 150816405 TTAATCTTTTACCTCATTTATTCACTCCTAGGAATAGTGGCCTAGCCCCTCCTGTAACCATTGTC TTAATCTTTTACCTCATTTATTCACTCCTAGGGATAGTGGCCTAGCCCCTCCTGTAACCATTGTC T C ARNT Ensembl:ENSG00000143437 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:150816376..150816425 26863196 MeRIP-seq:(Medium) rs587640516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858422,Human_RBP_ID_17338394 Human_Splice_Rec_127248,Human_Splice_Rec_127358,Human_Splice_Rec_127396 Human_miRNA_ID_2590511 RMVar_hsa_circ_106973,RMVar_hsa_circ_135939,RMVar_hsa_circ_341675,RMVar_hsa_circ_355353,RMVar_hsa_circ_368934,RMVar_hsa_circ_330599 93547 RMVar_ID_93547 Human_SNP_ID_33503036 m1A Human chr1 + 150817895 150817895 150817895 GCAAATGACCACCCCCTGGGTGACTGCTCAACAGATGATTATTTCACCCTTTTTTACCTGGGTGC GCAAATGACCACCCCCTGGGTGACTGCTCAACCGATGATTATTTCACCCTTTTTTACCTGGGTGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:150817892..150817972 26863196 MeRIP-seq:(Medium) rs749829643 Functional Loss SNV dbSNP153 33..33 33 - - - 93548 RMVar_ID_93548 Human_SNP_ID_33512398 m1A Human chr1 - 150858303 150858303 150858303 TAGTGTGTTATGAATATCTCTCCTATAAACCAACTTTAGTTGCTGAATTTATTTAGTTGCTGAAC TAGTGTGTTATGAATATCTCTCCTATAAACCACCTTTAGTTGCTGAATTTATTTAGTTGCTGAAC T G ARNT Ensembl:ENSG00000143437 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150858301..150858424 26863196 MeRIP-seq:(Medium) rs374503314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22904,RMVar_hsa_circ_4816,RMVar_hsa_circ_57485,RMVar_hsa_circ_54627,RMVar_hsa_circ_85968,RMVar_hsa_circ_135954,RMVar_hsa_circ_356276,RMVar_hsa_circ_378953 93549 RMVar_ID_93549 Human_SNP_ID_33539606 m1A Human chr1 - 150964508 150964508 150964508 TCCTGCCTGCTAGCACCACATTGGAAGGGATCATCTGGTCCAGAACCCCCATTTCTATCAACTAG TCCTGCCTGCTAGCACCACATTGGAAGGGATCGTCTGGTCCAGAACCCCCATTTCTATCAACTAG T C CERS2 Ensembl:ENSG00000143418 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150964457..150964558 32194978 MeRIP-seq:(Medium) rs1272710115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_127688 RMVar_hsa_circ_355252 93550 RMVar_ID_93550 Human_SNP_ID_33540061 m1A Human chr1 + 150966133 150966133 150966133 GTTCCTTGGCTTTATGCATTAATCTGGGAGGCAGCTGGAGTAATGGTTCAGTCATTCTTACGATG GTTCCTTGGCTTTATGCATTAATCTGGGAGGCGGCTGGAGTAATGGTTCAGTCATTCTTACGATG A G AL590133.2 Ensembl:ENSG00000259357 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:150966084..150966286 26863196 MeRIP-seq:(Medium) rs999420969 Functional Loss SNV dbSNP153 33..33 33 - - - 93551 RMVar_ID_93551 Human_SNP_ID_33540082 m1A Human chr1 + 150966176 150966176 150966176 TGGTTCAGTCATTCTTACGATGGTTGTTATTGAGGATGGGGTGGCCATTGGCTAGGGGCCGGCTC TGGTTCAGTCATTCTTACGATGGTTGTTATTGGGGATGGGGTGGCCATTGGCTAGGGGCCGGCTC A G AL590133.2 Ensembl:ENSG00000259357 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150966127..150966223 26863196 MeRIP-seq:(Medium) rs1166513857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3189481,Human_miRNA_ID_3204552 93552 RMVar_ID_93552 Human_SNP_ID_33540235 m1A Human chr1 - 150966621 150966621 150966621 TTCTCTCTCTCCTTGAATCCTCAGGATCCTGCATTGCACCCTGGTGTACCCACTGGAGCTCTATC TTCTCTCTCTCCTTGAATCCTCAGGATCCTGCGTTGCACCCTGGTGTACCCACTGGAGCTCTATC T C CERS2 Ensembl:ENSG00000143418 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150966601..150966878 32194978 MeRIP-seq:(Medium) rs753590439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21097,Human_RBP_ID_743226,Human_RBP_ID_4081096,Human_RBP_ID_17212304,Human_RBP_ID_17338408,Human_RBP_ID_17446024,Human_RBP_ID_18187254,Human_RBP_ID_22485859,Human_RBP_ID_23331777,Human_RBP_ID_26368168 Human_Splice_Rec_127684,Human_Splice_Rec_127706,Human_Splice_Rec_127716,Human_Splice_Rec_127734,Human_Splice_Rec_127754,Human_Splice_Rec_127774,Human_Splice_Rec_127786,Human_Splice_Rec_127804 RMVar_hsa_circ_135992,RMVar_hsa_circ_60340,RMVar_hsa_circ_122611,RMVar_hsa_circ_362748,RMVar_hsa_circ_135993,RMVar_hsa_circ_135994 93553 RMVar_ID_93553 Human_SNP_ID_33540767 m1A Human chr1 + 150968186 150968186 150968186 CTGGCGGCCAGAGAGCCCGCTCTGCCGGGACAAAAGCTCTACTTCCACCTGGGCACAGTGAAGAA CTGGCGGCCAGAGAGCCCGCTCTGCCGGGACAGAAGCTCTACTTCCACCTGGGCACAGTGAAGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150968045..150968225 26863196 MeRIP-seq:(Medium) rs1369232038 Functional Loss SNV dbSNP153 33..33 33 - - - 93554 RMVar_ID_93554 Human_SNP_ID_33540842 m1A Human chr1 + 150968379 150968379 150968379 CCACCAAACTCAGTGATTCCCAGAGCCAGAGCAGCATGCGGCTCATACCTGCTTGGGCTGCTTGC CCACCAAACTCAGTGATTCCCAGAGCCAGAGCGGCATGCGGCTCATACCTGCTTGGGCTGCTTGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr1:150968376..150968425;chr1:150968376..150968400 26863196,32194978 MeRIP-seq:(Medium) rs761512748 Functional Loss SNV dbSNP153 33..33 33 - - - 93555 RMVar_ID_93555 Human_SNP_ID_33540844 m1A Human chr1 + 150968382 150968382 150968382 CCAAACTCAGTGATTCCCAGAGCCAGAGCAGCATGCGGCTCATACCTGCTTGGGCTGCTTGCCAC CCAAACTCAGTGATTCCCAGAGCCAGAGCAGCTTGCGGCTCATACCTGCTTGGGCTGCTTGCCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150968380..150968457 26863196 MeRIP-seq:(Medium) rs969519210 Functional Loss SNV dbSNP153 33..33 33 - - - 93556 RMVar_ID_93556 Human_SNP_ID_33540903 m1A Human chr1 - 150968514 150968514 150968514 CAAGCTAGATACCTTACTCATATCCCTTCCCCAGGTACGTGGCTACACCACTGGCTGCCCTCTTG CAAGCTAGATACCTTACTCATATCCCTTCCCCCGGTACGTGGCTACACCACTGGCTGCCCTCTTG T G CERS2 Ensembl:ENSG00000143418 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150968476..150968525 26863196 MeRIP-seq:(Medium) rs745876310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5333645,Human_RBP_ID_5458534,Human_RBP_ID_22634282 RMVar_hsa_circ_135992,RMVar_hsa_circ_362748,RMVar_hsa_circ_135994,RMVar_hsa_circ_65260,RMVar_hsa_circ_73742,RMVar_hsa_circ_70057,RMVar_hsa_circ_354868 93557 RMVar_ID_93557 Human_SNP_ID_33542581 m1A Human chr1 - 150974719 150974719 150974719 CGGGCGCGGGCCGGCGGGCGGGCGGAAGAGGGAGGAGAGGCGCGGGGAGCCAGGCCTCGGGGCCT CGGGCGCGGGCCGGCGGGCGGGCGGAAGAGGGCGGAGAGGCGCGGGGAGCCAGGCCTCGGGGCCT T G CERS2 Ensembl:ENSG00000143418 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr1:150974444..150974850;chr1:150974542..150974850 26863196 MeRIP-seq:(Medium) rs1035645161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25145,Human_RBP_ID_224101,Human_RBP_ID_745056,Human_RBP_ID_3933962,Human_RBP_ID_4073014,Human_RBP_ID_5125279,Human_RBP_ID_5136357,Human_RBP_ID_5312664,Human_RBP_ID_5338350,Human_RBP_ID_8168300,Human_RBP_ID_8940015,Human_RBP_ID_9319137,Human_RBP_ID_9410654,Human_RBP_ID_17066656,Human_RBP_ID_17338420,Human_RBP_ID_18415056,Human_RBP_ID_18928574,Human_RBP_ID_22428574,Human_RBP_ID_22532150,Human_RBP_ID_22560186 93558 RMVar_ID_93558 Human_SNP_ID_33551318 m1A Human chr1 - 151008524 151008524 151008524 GCAGCCCGCCCGGGACTCAGGGACTAGAGGCCAGAGTCAGGAGGCGGGACTCGAACCCGCCACAC GCAGCCCGCCCGGGACTCAGGGACTAGAGGCCGGAGTCAGGAGGCGGGACTCGAACCCGCCACAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151008473..151008742 26863196 MeRIP-seq:(Medium) rs1028389870 Functional Loss SNV dbSNP153 33..33 33 - - - 93559 RMVar_ID_93559 Human_SNP_ID_33551327 m1A Human chr1 - 151008554 151008554 151008554 CCTGGTCGAGGAGAGGTTTCCCCGACGAATGCAGCCCGCCCGGGACTCAGGGACTAGAGGCCAGA CCTGGTCGAGGAGAGGTTTCCCCGACGAATGCCGCCCGCCCGGGACTCAGGGACTAGAGGCCAGA T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:151008457..151008631 26863410 MeRIP-seq:(Medium) rs1225560519 Functional Loss SNV dbSNP153 33..33 33 - - - 93560 RMVar_ID_93560 Human_SNP_ID_33551389 m1A Human chr1 + 151008697 151008697 151008697 TCTGCAGGTAACGAATCCCTGTCTGTGACTGTAAGGAATGGAGCACGGGGTCCAGGAAGGACGAA TCTGCAGGTAACGAATCCCTGTCTGTGACTGTGAGGAATGGAGCACGGGGTCCAGGAAGGACGAA A G PRUNE1 Ensembl:ENSG00000143363 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151008686..151008844 26863196 MeRIP-seq:(Medium) rs1463947100 Functional Loss SNV dbSNP153 33..33 33 - - - 93561 RMVar_ID_93561 Human_SNP_ID_33555696 m1A Human chr1 - 151025534 151025534 151025534 GTTGCCTTTCCAATTTTAAGGTCCATGTTGACACAGTCCAGGATGATGGTTCCTGTGGAGAAGGG GTTGCCTTTCCAATTTTAAGGTCCATGTTGACGCAGTCCAGGATGATGGTTCCTGTGGAGAAGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:151024655..151025572 32194978 MeRIP-seq:(Medium) rs1456845940 Functional Loss SNV dbSNP153 33..33 33 - - - 93562 RMVar_ID_93562 Human_SNP_ID_33561922 m1A Human chr1 + 151047829 151047829 151047829 AGGCAGGGCTTGCCTCACTGGCCACCCTCCCAACCCCAAGAGCCCAGCCCCATGGTCCCCGCCGC AGGCAGGGCTTGCCTCACTGGCCACCCTCCCACCCCCAAGAGCCCAGCCCCATGGTCCCCGCCGC A C C1orf56 Ensembl:ENSG00000143443 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151047780..151048027 26863196 MeRIP-seq:(Medium) rs751113549 Functional Loss SNV dbSNP153 33..33 33 - - - 93563 RMVar_ID_93563 Human_SNP_ID_33563375 m1A Human chr1 + 151053026 151053026 151053026 AAAAACAGGTGGCACCCAGACCATCATTCAGGAGACAGGAACTCATTCCAGGTTCCTAGAGAACT AAAAACAGGTGGCACCCAGACCATCATTCAGGCGACAGGAACTCATTCCAGGTTCCTAGAGAACT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151052663..151053062 32194978 MeRIP-seq:(Medium) rs938471046 Functional Loss SNV dbSNP153 33..33 33 - - - 93564 RMVar_ID_93564 Human_SNP_ID_33565102 m1A Human chr1 + 151060463 151060463 151060463 GAGTGAGAAGACAAAGCCGTCAAAGCCCCAACAGCTTTGTATTTCTCCAGCCCGGCGCAGACCCC GAGTGAGAAGACAAAGCCGTCAAAGCCCCAACGGCTTTGTATTTCTCCAGCCCGGCGCAGACCCC A G MLLT11 Ensembl:ENSG00000213190 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151060427..151060508 26863196 MeRIP-seq:(Medium) rs1335816829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26798848 Human_Splice_Rec_128269 Human_miRNA_ID_2404954,Human_miRNA_ID_2407949,Human_miRNA_ID_2410943,Human_miRNA_ID_2413924,Human_miRNA_ID_2622433,Human_miRNA_ID_2837008,Human_miRNA_ID_2854886 RMVar_hsa_circ_105255,RMVar_hsa_circ_136018 93565 RMVar_ID_93565 Human_SNP_ID_33565120 m1A Human chr1 - 151060541 151060538 151060542 CCTCCCTCAGTTTGGTTTACCTGTTATCAATCAATTACTGGCGTGTTCCAAAGATGGAGGGAGTG CCTCCCTCAGTTTGGTTTACCTGTTATCAAT____TACTGGCGTGTTCCAAAGATGGAGGGAGTG AATTG A CDC42SE1 Ensembl:ENSG00000197622 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151060490..151068342 32194978 MeRIP-seq:(Medium) rs1188302660 Functional Loss DEL dbSNP153 32..35 33 - - - 93566 RMVar_ID_93566 Human_SNP_ID_33580770 m1A Human chr1 + 151117986 151117986 151117986 CAGGAAGGCAATGAAAGAGAGCTACTACAGCAACAACTCCAGGAGGCCAATCGAAGAGCCCAGGA CAGGAAGGCAATGAAAGAGAGCTACTACAGCAGCAACTCCAGGAGGCCAATCGAAGAGCCCAGGA A G GABPB2 Ensembl:ENSG00000143458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151117958..151118049 26863196 MeRIP-seq:(Medium) rs1264066022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_128296,Human_Splice_Rec_128330,Human_Splice_Rec_128336 RMVar_hsa_circ_19016,RMVar_hsa_circ_288996,RMVar_hsa_circ_267228,RMVar_hsa_circ_136021,RMVar_hsa_circ_340094,RMVar_hsa_circ_300384,RMVar_hsa_circ_136030,RMVar_hsa_circ_136033,RMVar_hsa_circ_136034,RMVar_hsa_circ_330561,RMVar_hsa_circ_309381,RMVar_hsa_circ_136035 93567 RMVar_ID_93567 Human_SNP_ID_33593756 m1A Human chr1 + 151166525 151166525 151166525 TAGCCAGTTACATTCCAGAGGATGAGGCGCTGATGCTTCGGGATGGACGGTAAGAGCAAGGAGTG TAGCCAGTTACATTCCAGAGGATGAGGCGCTGGTGCTTCGGGATGGACGGTAAGAGCAAGGAGTG A G SCNM1 Ensembl:ENSG00000163156 Protein coding start codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151166477..151166577 32194978 MeRIP-seq:(Medium) rs151069031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850377,Human_RBP_ID_1411684,Human_RBP_ID_10576110 Human_Splice_Rec_128542,Human_Splice_Rec_128543,Human_Splice_Rec_128554,Human_Splice_Rec_128555,Human_Splice_Rec_128562,Human_Splice_Rec_128564,Human_Splice_Rec_128565,Human_Splice_Rec_128576,Human_Splice_Rec_128577 RMVar_hsa_circ_102632,RMVar_hsa_circ_136044 93568 RMVar_ID_93568 Human_SNP_ID_33593757 m1A Human chr1 + 151166525 151166525 151166525 TAGCCAGTTACATTCCAGAGGATGAGGCGCTGATGCTTCGGGATGGACGGTAAGAGCAAGGAGTG TAGCCAGTTACATTCCAGAGGATGAGGCGCTGTTGCTTCGGGATGGACGGTAAGAGCAAGGAGTG A T SCNM1 Ensembl:ENSG00000163156 Protein coding start codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151166477..151166577 32194978 MeRIP-seq:(Medium) rs151069031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850377,Human_RBP_ID_1411684,Human_RBP_ID_10576110 Human_Splice_Rec_128542,Human_Splice_Rec_128543,Human_Splice_Rec_128554,Human_Splice_Rec_128555,Human_Splice_Rec_128562,Human_Splice_Rec_128564,Human_Splice_Rec_128565,Human_Splice_Rec_128576,Human_Splice_Rec_128577 RMVar_hsa_circ_102632,RMVar_hsa_circ_136044 93569 RMVar_ID_93569 Human_SNP_ID_33596626 m1A Human chr1 + 151176744 151176744 151176744 GGCCGGGGCCCAGGGCTGAGGCAGTGGGCGGCAGTCCATGGGCAGTAATGTACTTCTTGTAAGCC GGCCGGGGCCCAGGGCTGAGGCAGTGGGCGGCGGTCCATGGGCAGTAATGTACTTCTTGTAAGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151176501..151177000 26863196 MeRIP-seq:(Medium) rs1289963250 Functional Loss SNV dbSNP153 33..33 33 - - - 93570 RMVar_ID_93570 Human_SNP_ID_33596699 m1A Human chr1 + 151176938 151176938 151176938 AACCATTCCTCGAAAGTTGCATCATCACTAAAAGTGATGAAGGTACGTGAGCAGCGAGCAGGGGG AACCATTCCTCGAAAGTTGCATCATCACTAAAGGTGATGAAGGTACGTGAGCAGCGAGCAGGGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151176534..151178150 26863196 MeRIP-seq:(Medium) rs28405665 Functional Loss SNV dbSNP153 33..33 33 - - - 93571 RMVar_ID_93571 Human_SNP_ID_33599784 m1A Human chr1 - 151190137 151190137 151190137 CCGAGCTGGTGAGGGGCTGCAGGTGGCGGCGCAGTCTCGGTAGGCGGTATGAGTTTGGCTGGGGG CCGAGCTGGTGAGGGGCTGCAGGTGGCGGCGCGGTCTCGGTAGGCGGTATGAGTTTGGCTGGGGG T C VPS72 Ensembl:ENSG00000163159 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:151185776..151190200;chr1:151185801..151190200 26863196 MeRIP-seq:(Medium) rs1229056741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074383,Human_RBP_ID_5109201,Human_RBP_ID_5688960,Human_RBP_ID_9270321,Human_RBP_ID_23332104 Human_Splice_Rec_128681 Human_miRNA_ID_3085130 RMVar_hsa_circ_119046,RMVar_hsa_circ_136056 93572 RMVar_ID_93572 Human_SNP_ID_33602063 m1A Human chr1 + 151198624 151198624 151198624 GGCGATTAACAGGCCGTGGTTAGGAAGGACGGAGAAGGGGCGTTCGCTCCTTTGGGACTTTTCAT GGCGATTAACAGGCCGTGGTTAGGAAGGACGGGGAAGGGGCGTTCGCTCCTTTGGGACTTTTCAT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:151198576..151198759 26863196 MeRIP-seq:(Medium) rs958295693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224095,Human_RBP_ID_4076988,Human_RBP_ID_5688970,Human_RBP_ID_9554966,Human_RBP_ID_10576389,Human_RBP_ID_18415059,Human_RBP_ID_22127531,Human_RBP_ID_24447231,Human_RBP_ID_24586393,Human_RBP_ID_26841459 93573 RMVar_ID_93573 Human_SNP_ID_33602102 m1A Human chr1 - 151198763 151198763 151198763 GAACTCACGTCCCGCACCCCCTCCACAAGTTTAACCGCTTTCCACAGGGGATACTTTCCCCTTTC GAACTCACGTCCCGCACCCCCTCCACAAGTTTCACCGCTTTCCACAGGGGATACTTTCCCCTTTC T G lnc-VPS72-1 RNACentral:URS0000D5BB4F lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151198576..151198825;chr1:151198551..151198800;chr1:151198551..151199370 26863196 MeRIP-seq:(Medium) rs1176470187 Functional Loss SNV dbSNP153 33..33 33 - - - 93574 RMVar_ID_93574 Human_SNP_ID_33602281 m1A Human chr1 - 151199176 151199176 151199176 GCCCAGCTCGCGCCCACTTACCGGTAACACGTAGGACATTCCCAGCTACAGGTACCCTCTTAGGT GCCCAGCTCGCGCCCACTTACCGGTAACACGTGGGACATTCCCAGCTACAGGTACCCTCTTAGGT T C lnc-VPS72-1 RNACentral:URS0000D5BB4F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151199125..151199197 26863196 MeRIP-seq:(Medium) rs1392752902 Functional Loss SNV dbSNP153 33..33 33 - - - 93575 RMVar_ID_93575 Human_SNP_ID_33602416 m1A Human chr1 + 151199647 151199646 151199648 AAAAAAAAAAAAAAGAAGTTGCGGTAGGAAACAAGAGAAACGGAAGGGAGTAGAGAAACTAAGAA AAAAAAAAAAAAAAGAAGTTGCGGTAGGAAAC__GAGAAACGGAAGGGAGTAGAGAAACTAAGAA CAA C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151199596..151199867 26863196 MeRIP-seq:(Medium) rs952247201 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9554969,Human_RBP_ID_10576435,Human_RBP_ID_22846811 93576 RMVar_ID_93576 Human_SNP_ID_33602420 m1A Human chr1 + 151199650 151199650 151199650 AAAAAAAAAAAGAAGTTGCGGTAGGAAACAAGAGAAACGGAAGGGAGTAGAGAAACTAAGAAAGT AAAAAAAAAAAGAAGTTGCGGTAGGAAACAAGGGAAACGGAAGGGAGTAGAGAAACTAAGAAAGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:151199621..151199818;chr1:151199606..151199888 26863196 MeRIP-seq:(Medium) rs145727504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9554969,Human_RBP_ID_10576435,Human_RBP_ID_22846811 93577 RMVar_ID_93577 Human_SNP_ID_33617444 m1A Human chr1 + 151254798 151254798 151254798 GGGAGGAAGGTGGCAAGATGGTGTTGGAAAGCACTATGGTGTGGTGAGGAGCTACTTCGGGGCAG GGGAGGAAGGTGGCAAGATGGTGTTGGAAAGCGCTATGGTGTGGTGAGGAGCTACTTCGGGGCAG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151254726..151254970 26863196 MeRIP-seq:(Medium) rs990243239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326203,Human_RBP_ID_745283,Human_RBP_ID_4073020,Human_RBP_ID_18187263,Human_RBP_ID_18415995,Human_RBP_ID_19039117,Human_RBP_ID_22430909,Human_RBP_ID_23205330,Human_RBP_ID_23332276,Human_RBP_ID_26311804 Human_Splice_Rec_128901,Human_Splice_Rec_128919,Human_Splice_Rec_128937,Human_Splice_Rec_128939,Human_Splice_Rec_128947 93578 RMVar_ID_93578 Human_SNP_ID_33617446 m1A Human chr1 - 151254800 151254800 151254800 TCCTGCCCCGAAGTAGCTCCTCACCACACCATAGTGCTTTCCAACACCATCTTGCCACCTTCCTC TCCTGCCCCGAAGTAGCTCCTCACCACACCATGGTGCTTTCCAACACCATCTTGCCACCTTCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151254726..151255004 26863196 MeRIP-seq:(Medium) rs1215292077 Functional Loss SNV dbSNP153 33..33 33 - - - 93579 RMVar_ID_93579 Human_SNP_ID_33617447 m1A Human chr1 + 151254801 151254801 151254801 AGGAAGGTGGCAAGATGGTGTTGGAAAGCACTATGGTGTGGTGAGGAGCTACTTCGGGGCAGGAG AGGAAGGTGGCAAGATGGTGTTGGAAAGCACTGTGGTGTGGTGAGGAGCTACTTCGGGGCAGGAG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:151254751..151254859 26863410 MeRIP-seq:(Medium) rs754892033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326203,Human_RBP_ID_4073020,Human_RBP_ID_11183521,Human_RBP_ID_18187263,Human_RBP_ID_18415995,Human_RBP_ID_19039117,Human_RBP_ID_22430909,Human_RBP_ID_23205330,Human_RBP_ID_23332276,Human_RBP_ID_26311804 Human_Splice_Rec_128901,Human_Splice_Rec_128919,Human_Splice_Rec_128937,Human_Splice_Rec_128939,Human_Splice_Rec_128947 93580 RMVar_ID_93580 Human_SNP_ID_33617452 m1A Human chr1 - 151254807 151254807 151254807 CTGCCCCTCCTGCCCCGAAGTAGCTCCTCACCACACCATAGTGCTTTCCAACACCATCTTGCCAC CTGCCCCTCCTGCCCCGAAGTAGCTCCTCACCGCACCATAGTGCTTTCCAACACCATCTTGCCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:151254801..151259155 32194978 MeRIP-seq:(Medium) rs1558318702 Functional Loss SNV dbSNP153 33..33 33 - - - 93581 RMVar_ID_93581 Human_SNP_ID_33619391 m1A Human chr1 + 151262122 151262122 151262122 TGGAACTGGAGAGAAGGTTTTGGAAAACTTCTACATTTCTTCTCTCTTGTCCTTCAACCCTAATC TGGAACTGGAGAGAAGGTTTTGGAAAACTTCTGCATTTCTTCTCTCTTGTCCTTCAACCCTAATC A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:151262118..151262325 26863410 MeRIP-seq:(Medium) rs1394587752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101942,Human_RBP_ID_22015844,Human_RBP_ID_22536267,Human_RBP_ID_24587265 93582 RMVar_ID_93582 Human_SNP_ID_33619794 m1A Human chr1 + 151263905 151263905 151263905 TGCTGACCTGAATTCACTGAAATGCTTTTCCTACATCCCAGTGACTGTGAAGTGCTGACCACACT TGCTGACCTGAATTCACTGAAATGCTTTTCCTGCATCCCAGTGACTGTGAAGTGCTGACCACACT A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151263901..151263975 26863196 MeRIP-seq:(Medium) rs1450718607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2093901,Human_RBP_ID_3281256,Human_RBP_ID_10578514,Human_RBP_ID_18551426,Human_RBP_ID_19039119 RMVar_hsa_circ_136084,RMVar_hsa_circ_25805,RMVar_hsa_circ_271856,RMVar_hsa_circ_373184,RMVar_hsa_circ_373456,RMVar_hsa_circ_354212,RMVar_hsa_circ_114455,RMVar_hsa_circ_136086,RMVar_hsa_circ_136087,RMVar_hsa_circ_136085 93583 RMVar_ID_93583 Human_SNP_ID_33620406 m1A Human chr1 + 151266050 151266050 151266050 TATGGAAGAGCAGCGGCAGCGGCAGGAGGAGGAGGCCCGGCGGGCAGCTGCAGCTTCTGCTGCTG TATGGAAGAGCAGCGGCAGCGGCAGGAGGAGGGGGCCCGGCGGGCAGCTGCAGCTTCTGCTGCTG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:151265505..151266100 32194978 MeRIP-seq:(Medium) rs754574405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222537,Human_RBP_ID_326216,Human_RBP_ID_855204,Human_RBP_ID_5158814,Human_RBP_ID_9270322,Human_RBP_ID_17762872,Human_RBP_ID_21879210 Human_Splice_Rec_128912,Human_Splice_Rec_128913,Human_Splice_Rec_128930,Human_Splice_Rec_128931,Human_Splice_Rec_128958,Human_Splice_Rec_128978,Human_Splice_Rec_128979,Human_Splice_Rec_128986 RMVar_hsa_circ_37876,RMVar_hsa_circ_136084,RMVar_hsa_circ_373184,RMVar_hsa_circ_354212,RMVar_hsa_circ_114455,RMVar_hsa_circ_136085,RMVar_hsa_circ_89368,RMVar_hsa_circ_136088,RMVar_hsa_circ_79232,RMVar_hsa_circ_103510,RMVar_hsa_circ_136089,RMVar_hsa_circ_320402,RMVar_hsa_circ_377694,RMVar_hsa_circ_377759,RMVar_hsa_circ_136092,RMVar_hsa_circ_136093,RMVar_hsa_circ_136091,RMVar_hsa_circ_96708,RMVar_hsa_circ_113113,RMVar_hsa_circ_136094,RMVar_hsa_circ_136095 93584 RMVar_ID_93584 Human_SNP_ID_33620417 m1A Human chr1 - 151266081 151266081 151266081 CCTTCAGTCCCAGTCGTAGCAATCCCGGCCTCAGCAGCAGAAGCTGCAGCTGCCCGCCGGGCCTC CCTTCAGTCCCAGTCGTAGCAATCCCGGCCTCCGCAGCAGAAGCTGCAGCTGCCCGCCGGGCCTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151266035..151266116 26863196 MeRIP-seq:(Medium) rs1248303832 Functional Loss SNV dbSNP153 33..33 33 - - - 93585 RMVar_ID_93585 Human_SNP_ID_33620513 m1A Human chr1 + 151266401 151266401 151266401 TCCTGACCTAAGCAGTATGACTGAGGAAGAGCAGATTGCTTATGCCATGCAGATGTCCCTGCAGG TCCTGACCTAAGCAGTATGACTGAGGAAGAGCGGATTGCTTATGCCATGCAGATGTCCCTGCAGG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:151266326..151266400;chr1:151266296..151266525 32194978 MeRIP-seq:(Medium) rs768787222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1455,Human_RBP_ID_971200,Human_RBP_ID_1411775,Human_RBP_ID_4081290,Human_RBP_ID_5136359,Human_RBP_ID_5689415,Human_RBP_ID_8956018,Human_RBP_ID_10578536,Human_RBP_ID_23332308 Human_Splice_Rec_128914,Human_Splice_Rec_128915,Human_Splice_Rec_128932,Human_Splice_Rec_128933,Human_Splice_Rec_128959,Human_Splice_Rec_128980,Human_Splice_Rec_128981,Human_Splice_Rec_128988,Human_Splice_Rec_128989,Human_Splice_Rec_128993 RMVar_hsa_circ_37876,RMVar_hsa_circ_136084,RMVar_hsa_circ_354212,RMVar_hsa_circ_114455,RMVar_hsa_circ_136088,RMVar_hsa_circ_79232,RMVar_hsa_circ_103510,RMVar_hsa_circ_136089,RMVar_hsa_circ_320402,RMVar_hsa_circ_377694,RMVar_hsa_circ_377759,RMVar_hsa_circ_136092,RMVar_hsa_circ_136093,RMVar_hsa_circ_96708,RMVar_hsa_circ_113113,RMVar_hsa_circ_136094,RMVar_hsa_circ_136095 93586 RMVar_ID_93586 Human_SNP_ID_33620773 m1A Human chr1 + 151267312 151267310 151267313 CTCCCTGGCCTCCCAGGCCACCAAGGACGGCAAGAAGGACAAGAAGGAGGAAGACAAGAAGTGAG CTCCCTGGCCTCCCAGGCCACCAAGGACGGC___AAGGACAAGAAGGAGGAAGACAAGAAGTGAG CAAG C PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:151267185..151267400 26863196 MeRIP-seq:(Medium) rs1315647267 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_326224,Human_RBP_ID_858897,Human_RBP_ID_3936592,Human_RBP_ID_22427497,Human_RBP_ID_26311805,Human_RBP_ID_27800771 Human_miRNA_ID_655331,Human_miRNA_ID_2253913 RMVar_hsa_circ_103510,RMVar_hsa_circ_136089,RMVar_hsa_circ_377694,RMVar_hsa_circ_377759,RMVar_hsa_circ_136092,RMVar_hsa_circ_136093,RMVar_hsa_circ_96708,RMVar_hsa_circ_113113,RMVar_hsa_circ_136094,RMVar_hsa_circ_136095 93587 RMVar_ID_93587 Human_SNP_ID_33620777 m1A Human chr1 + 151267323 151267323 151267323 CCCAGGCCACCAAGGACGGCAAGAAGGACAAGAAGGAGGAAGACAAGAAGTGAGACTGGAGGGAA CCCAGGCCACCAAGGACGGCAAGAAGGACAAGGAGGAGGAAGACAAGAAGTGAGACTGGAGGGAA A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs996715839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259013,Human_RBP_ID_22427497,Human_RBP_ID_26311805,Human_RBP_ID_27800772 RMVar_hsa_circ_103510,RMVar_hsa_circ_136089,RMVar_hsa_circ_377694,RMVar_hsa_circ_377759,RMVar_hsa_circ_136092,RMVar_hsa_circ_136093,RMVar_hsa_circ_96708,RMVar_hsa_circ_113113,RMVar_hsa_circ_136094,RMVar_hsa_circ_136095 93588 RMVar_ID_93588 Human_SNP_ID_33620780 m1A Human chr1 + 151267327 151267327 151267327 GGCCACCAAGGACGGCAAGAAGGACAAGAAGGAGGAAGACAAGAAGTGAGACTGGAGGGAAAGGG GGCCACCAAGGACGGCAAGAAGGACAAGAAGGGGGAAGACAAGAAGTGAGACTGGAGGGAAAGGG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151267276..151267425 32194978 MeRIP-seq:(Medium) rs1064203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259013,Human_RBP_ID_22427497,Human_RBP_ID_26311805,Human_RBP_ID_27798514 RMVar_hsa_circ_103510,RMVar_hsa_circ_136089,RMVar_hsa_circ_377694,RMVar_hsa_circ_377759,RMVar_hsa_circ_136092,RMVar_hsa_circ_136093,RMVar_hsa_circ_96708,RMVar_hsa_circ_113113,RMVar_hsa_circ_136094,RMVar_hsa_circ_136095 93589 RMVar_ID_93589 Human_SNP_ID_33620792 m1A Human chr1 - 151267370 151267370 151267370 ATATTCCGTGCTTCCCATGCAGTCCCCTAAGCAGACTCAGCTACCCTTTCCCTCCAGTCTCACTT ATATTCCGTGCTTCCCATGCAGTCCCCTAAGCCGACTCAGCTACCCTTTCCCTCCAGTCTCACTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151267151..151267450;chr1:151267201..151267450 26863196 MeRIP-seq:(Medium) rs185955158 Functional Loss SNV dbSNP153 33..33 33 - - - 93590 RMVar_ID_93590 Human_SNP_ID_33624757 m1A Human chr1 + 151281633 151281633 151281633 AGAGGGAGGAGCGACGGGTTACGCTGTCGCCCAGGAGCTGAACCGCGCGAGGACCCCATCCATCA AGAGGGAGGAGCGACGGGTTACGCTGTCGCCCCGGAGCTGAACCGCGCGAGGACCCCATCCATCA A C ZNF687 Ensembl:ENSG00000143373 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151281594..151281690 26863196 MeRIP-seq:(Medium) rs747172005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1250182,Human_RBP_ID_1411782,Human_RBP_ID_5412953 93591 RMVar_ID_93591 Human_SNP_ID_33624758 m1A Human chr1 + 151281633 151281633 151281633 AGAGGGAGGAGCGACGGGTTACGCTGTCGCCCAGGAGCTGAACCGCGCGAGGACCCCATCCATCA AGAGGGAGGAGCGACGGGTTACGCTGTCGCCCGGGAGCTGAACCGCGCGAGGACCCCATCCATCA A G ZNF687 Ensembl:ENSG00000143373 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151281594..151281690 26863196 MeRIP-seq:(Medium) rs747172005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1250182,Human_RBP_ID_1411782,Human_RBP_ID_5412953 93592 RMVar_ID_93592 Human_SNP_ID_33624989 m1A Human chr1 + 151282339 151282339 151282339 GCGGCGGCCGCGGGGAGGGCGGCGGTGGCTGCAGCGGCTGGAGCGGGGTAGAGACCGCCGGGTCT GCGGCGGCCGCGGGGAGGGCGGCGGTGGCTGCGGCGGCTGGAGCGGGGTAGAGACCGCCGGGTCT A G ZNF687 Ensembl:ENSG00000143373 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151282230..151282396 26863196 MeRIP-seq:(Medium) rs1326968741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224075,Human_RBP_ID_3993289,Human_RBP_ID_5519158,Human_RBP_ID_8227822,Human_RBP_ID_8940016 Human_Splice_Rec_129009,Human_Splice_Rec_129021,Human_Splice_Rec_129037 93593 RMVar_ID_93593 Human_SNP_ID_33625549 m1A Human chr1 - 151284216 151284216 151284216 CTGCCACAGTGGGAAAAAGCCAGGCTCCCTCAACCCTCACCCATCATTTCTGCTCCAAGCTCCTC CTGCCACAGTGGGAAAAAGCCAGGCTCCCTCAGCCCTCACCCATCATTTCTGCTCCAAGCTCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151284214..151284294 26863196 MeRIP-seq:(Medium) rs1218244778 Functional Loss SNV dbSNP153 33..33 33 - - - 93594 RMVar_ID_93594 Human_SNP_ID_33626383 m1A Human chr1 + 151287059 151287059 151287059 ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCAGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCC ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCCGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCC A C ZNF687 Ensembl:ENSG00000143373 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151287009..151287079 26863196 MeRIP-seq:(Medium) rs768168409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26368340,Human_RBP_ID_27168005 RMVar_hsa_circ_266724 93595 RMVar_ID_93595 Human_SNP_ID_33626384 m1A Human chr1 + 151287059 151287059 151287059 ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCAGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCC ACGGACATCCCTGCCAGTGCCTCGCCTCCCCCGGTTGCTGGGGTGCCCTTCTTCAAGCAGTCTCC A G ZNF687 Ensembl:ENSG00000143373 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151287009..151287079 26863196 MeRIP-seq:(Medium) rs768168409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26368340,Human_RBP_ID_27168005 RMVar_hsa_circ_266724 93596 RMVar_ID_93596 Human_SNP_ID_33627177 m1A Human chr1 - 151289224 151289224 151289224 TGGAAGCTGGGATGCTGGGAGTAGAGGTGGGCATGGGCACTTGGCCCAGACTTGAAGGCCATGGG TGGAAGCTGGGATGCTGGGAGTAGAGGTGGGCGTGGGCACTTGGCCCAGACTTGAAGGCCATGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151289126..151289275 26863196 MeRIP-seq:(Medium) rs111833417 Functional Loss SNV dbSNP153 33..33 33 - - - 93597 RMVar_ID_93597 Human_SNP_ID_33640362 m1A Human chr1 + 151342283 151342283 151342283 TTAAGTCTTTATTACCCTGTGGTGCAGTGTCTACCTCTCCCTTTGCCAAAGGAAAAGCCTCCTTT TTAAGTCTTTATTACCCTGTGGTGCAGTGTCTGCCTCTCCCTTTGCCAAAGGAAAAGCCTCCTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151342234..151342334 32194978 MeRIP-seq:(Medium) rs762798581 Functional Loss SNV dbSNP153 33..33 33 - - - 93598 RMVar_ID_93598 Human_SNP_ID_33641809 m1A Human chr1 - 151347135 151347135 151347135 AAGGCGACTGTTCAGAGGTAGGGAGGGGCAAGATGAGTTGGGAGGAGAGCAGAAAAAGATTGTAG AAGGCGACTGTTCAGAGGTAGGGAGGGGCAAGGTGAGTTGGGAGGAGAGCAGAAAAAGATTGTAG T C RFX5 Ensembl:ENSG00000143390 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151347132..151347275 26863196 MeRIP-seq:(Medium) rs949528560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23332410 93599 RMVar_ID_93599 Human_SNP_ID_33645960 m1A Human chr1 - 151364502 151364502 151364502 CTCATCACCCACACTCCCTATTTTGGGCCCTCACTTCCTTGGGGACCTGGCTTCATTCTGCTCTC CTCATCACCCACACTCCCTATTTTGGGCCCTCGCTTCCTTGGGGACCTGGCTTCATTCTGCTCTC T C SELENBP1 Ensembl:ENSG00000143416 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151364452..151364650 26863196 MeRIP-seq:(Medium) rs1188031490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326373,Human_RBP_ID_5109206,Human_RBP_ID_17339085,Human_RBP_ID_17647649,Human_RBP_ID_18157823,Human_RBP_ID_24447265 Human_miRNA_ID_188248 RMVar_hsa_circ_87249,RMVar_hsa_circ_136109,RMVar_hsa_circ_85190,RMVar_hsa_circ_136108 93600 RMVar_ID_93600 Human_SNP_ID_33647244 m1A Human chr1 + 151368180 151368178 151368180 CACATTTCACAGCTGTGGAAGTTTTCATGAGCACACAGTGCTGGCAGGTACCTTTGCCATTGCCC CACATTTCACAGCTGTGGAAGTTTTCATGAG__CACAGTGCTGGCAGGTACCTTTGCCATTGCCC GCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151368178..151368274 26863196 MeRIP-seq:(Medium) rs780328331 Functional Loss DEL dbSNP153 32..33 33 - - - 93601 RMVar_ID_93601 Human_SNP_ID_33647246 m1A Human chr1 + 151368180 151368180 151368180 CACATTTCACAGCTGTGGAAGTTTTCATGAGCACACAGTGCTGGCAGGTACCTTTGCCATTGCCC CACATTTCACAGCTGTGGAAGTTTTCATGAGCGCACAGTGCTGGCAGGTACCTTTGCCATTGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151368178..151368274 26863196 MeRIP-seq:(Medium) rs1402167328 Functional Loss SNV dbSNP153 33..33 33 - - - 93602 RMVar_ID_93602 Human_SNP_ID_33647247 m1A Human chr1 + 151368180 151368180 151368180 CACATTTCACAGCTGTGGAAGTTTTCATGAGCACACAGTGCTGGCAGGTACCTTTGCCATTGCCC CACATTTCACAGCTGTGGAAGTTTTCATGAGCTCACAGTGCTGGCAGGTACCTTTGCCATTGCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151368178..151368274 26863196 MeRIP-seq:(Medium) rs1402167328 Functional Loss SNV dbSNP153 33..33 33 - - - 93603 RMVar_ID_93603 Human_SNP_ID_33655018 m1A Human chr1 + 151399666 151399666 151399666 CGGCCCCAGGACAGTTTTACCGCATTCCGTCCACTCCCGATTCCTTCATGGATCCGGCGTCTGCA CGGCCCCAGGACAGTTTTACCGCATTCCGTCCGCTCCCGATTCCTTCATGGATCCGGCGTCTGCA A G PSMB4 Ensembl:ENSG00000159377 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:151399566..151400081 26863410 MeRIP-seq:(Medium) rs1381259372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858880,Human_RBP_ID_3993741,Human_RBP_ID_5137190,Human_RBP_ID_5155694,Human_RBP_ID_11183599,Human_RBP_ID_22427499,Human_RBP_ID_22780020,Human_RBP_ID_26389782,Human_RBP_ID_26841700,Human_RBP_ID_27168096 Human_Splice_Rec_129743,Human_Splice_Rec_129747,Human_Splice_Rec_129759,Human_Splice_Rec_129765,Human_Splice_Rec_129767 Human_miRNA_ID_1969167,Human_miRNA_ID_2134810 RMVar_hsa_circ_77086,RMVar_hsa_circ_136111 93604 RMVar_ID_93604 Human_SNP_ID_33655028 m1A Human chr1 + 151399698 151399698 151399698 ACTCCCGATTCCTTCATGGATCCGGCGTCTGCACTTTACAGAGGTCCAATCACGCGGACCCAGTA ACTCCCGATTCCTTCATGGATCCGGCGTCTGCCCTTTACAGAGGTCCAATCACGCGGACCCAGTA A C PSMB4 Ensembl:ENSG00000159377 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:151399576..151400113 26863196 MeRIP-seq:(Medium) rs755459175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326386,Human_RBP_ID_743624,Human_RBP_ID_858880,Human_RBP_ID_4075943,Human_RBP_ID_5137190,Human_RBP_ID_5484357,Human_RBP_ID_10579482,Human_RBP_ID_17725697,Human_RBP_ID_18204514,Human_RBP_ID_18551502,Human_RBP_ID_22427499,Human_RBP_ID_22485904,Human_RBP_ID_23332420,Human_RBP_ID_27388146 Human_Splice_Rec_129743,Human_Splice_Rec_129747,Human_Splice_Rec_129759,Human_Splice_Rec_129765,Human_Splice_Rec_129767 Human_miRNA_ID_1940998,Human_miRNA_ID_1944054,Human_miRNA_ID_2115189,Human_miRNA_ID_2198763,Human_miRNA_ID_2201833,Human_miRNA_ID_2804780,Human_miRNA_ID_2807925,Human_miRNA_ID_2811069,Human_miRNA_ID_2814296,Human_miRNA_ID_2861555,Human_miRNA_ID_3111283 RMVar_hsa_circ_77086,RMVar_hsa_circ_136111 93605 RMVar_ID_93605 Human_SNP_ID_33655029 m1A Human chr1 + 151399698 151399698 151399698 ACTCCCGATTCCTTCATGGATCCGGCGTCTGCACTTTACAGAGGTCCAATCACGCGGACCCAGTA ACTCCCGATTCCTTCATGGATCCGGCGTCTGCGCTTTACAGAGGTCCAATCACGCGGACCCAGTA A G PSMB4 Ensembl:ENSG00000159377 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:151399576..151400113 26863196 MeRIP-seq:(Medium) rs755459175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326386,Human_RBP_ID_743624,Human_RBP_ID_858880,Human_RBP_ID_4075943,Human_RBP_ID_5137190,Human_RBP_ID_5484357,Human_RBP_ID_10579482,Human_RBP_ID_17725697,Human_RBP_ID_18204514,Human_RBP_ID_18551502,Human_RBP_ID_22427499,Human_RBP_ID_22485904,Human_RBP_ID_23332420,Human_RBP_ID_27388146 Human_Splice_Rec_129743,Human_Splice_Rec_129747,Human_Splice_Rec_129759,Human_Splice_Rec_129765,Human_Splice_Rec_129767 Human_miRNA_ID_1940998,Human_miRNA_ID_1944054,Human_miRNA_ID_2115189,Human_miRNA_ID_2198763,Human_miRNA_ID_2201833,Human_miRNA_ID_2804780,Human_miRNA_ID_2807925,Human_miRNA_ID_2811069,Human_miRNA_ID_2814296,Human_miRNA_ID_2861555,Human_miRNA_ID_3111283 RMVar_hsa_circ_77086,RMVar_hsa_circ_136111 93606 RMVar_ID_93606 Human_SNP_ID_33655037 m1A Human chr1 + 151399727 151399727 151399727 TGCACTTTACAGAGGTCCAATCACGCGGACCCAGTAAGTTCTCGGCGCTTTCGTTTGCGTAGCGG TGCACTTTACAGAGGTCCAATCACGCGGACCCGGTAAGTTCTCGGCGCTTTCGTTTGCGTAGCGG A G PSMB4 Ensembl:ENSG00000159377 Protein coding exon GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr1:151399676..151399750 26863196,32194978 MeRIP-seq:(Medium) rs1308655589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743624,Human_RBP_ID_5137190,Human_RBP_ID_10579488,Human_RBP_ID_19039141,Human_RBP_ID_22427500 Human_Splice_Rec_129743,Human_Splice_Rec_129747,Human_Splice_Rec_129759,Human_Splice_Rec_129765,Human_Splice_Rec_129767 RMVar_hsa_circ_77086,RMVar_hsa_circ_136111 93607 RMVar_ID_93607 Human_SNP_ID_33655635 m1A Human chr1 - 151401529 151401526 151401529 GTGACAGTGGCGATTTGAAACTGGAAGAAAGCAGAGCATTCAATAATGCCCACGCCTTAAGTCCT GTGACAGTGGCGATTTGAAACTGGAAGAAAGC___GCATTCAATAATGCCCACGCCTTAAGTCCT CTCT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151401526..151401650 32194978 MeRIP-seq:(Medium) rs1418577748 Functional Loss DEL dbSNP153 33..35 33 - - - 93608 RMVar_ID_93608 Human_SNP_ID_33655636 m1A Human chr1 - 151401529 151401527 151401530 GTGACAGTGGCGATTTGAAACTGGAAGAAAGCAGAGCATTCAATAATGCCCACGCCTTAAGTCCT GTGACAGTGGCGATTTGAAACTGGAAGAAAG___AGCATTCAATAATGCCCACGCCTTAAGTCCT TCTG T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151401526..151401650 32194978 MeRIP-seq:(Medium) rs755122811 Functional Loss DEL dbSNP153 32..34 33 - - - 93609 RMVar_ID_93609 Human_SNP_ID_33657714 m1A Human chr1 - 151408479 151408479 151408479 CCTTGCAGGAGGCAGCACCGCTGACCTCCTCAATGGACCCTCTGCCTGTCTTCCTTTATCCCCCT CCTTGCAGGAGGCAGCACCGCTGACCTCCTCAGTGGACCCTCTGCCTGTCTTCCTTTATCCCCCT T C POGZ Ensembl:ENSG00000143442 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:151408401..151408581 26863196 MeRIP-seq:(Medium) rs760122079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8735011,Human_RBP_ID_9359319,Human_RBP_ID_18929969,Human_RBP_ID_22427507 Human_Splice_Rec_129807,Human_Splice_Rec_129841,Human_Splice_Rec_129875,Human_Splice_Rec_129907,Human_Splice_Rec_129943,Human_Splice_Rec_129977,Human_Splice_Rec_130011,Human_Splice_Rec_130027 Human_miRNA_ID_2271095,Human_miRNA_ID_3056643 RMVar_hsa_circ_94373,RMVar_hsa_circ_338382,RMVar_hsa_circ_136122,RMVar_hsa_circ_373774,RMVar_hsa_circ_136123,RMVar_hsa_circ_361867,RMVar_hsa_circ_32445,RMVar_hsa_circ_292373,RMVar_hsa_circ_136124,RMVar_hsa_circ_136125 93610 RMVar_ID_93610 Human_SNP_ID_33671370 m1A Human chr1 + 151458504 151458501 151458505 ATTACATAACACAAGGGATCGGCTCAGCAATCACTCATTTTCCTCCTCCCGCTCAAAACGAGCGC ATTACATAACACAAGGGATCGGCTCAGCAA____TCATTTTCCTCCTCCCGCTCAAAACGAGCGC ATCAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:151458477..151458573 26863196 MeRIP-seq:(Medium) rs1350884021 Functional Loss DEL dbSNP153 31..34 33 - - - 93611 RMVar_ID_93611 Human_SNP_ID_33671660 m1A Human chr1 + 151458866 151458866 151458866 CGCCGGGGGGCGGGGGCGGCCGGCCAGCCGGCAGGCAGGGACCTCCGCCGCCGGCCCTTCGCGCG CGCCGGGGGGCGGGGGCGGCCGGCCAGCCGGCCGGCAGGGACCTCCGCCGCCGGCCCTTCGCGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151458853..151459067 26863196 MeRIP-seq:(Medium) rs1157424561 Functional Loss SNV dbSNP153 33..33 33 - - - 93612 RMVar_ID_93612 Human_SNP_ID_33671661 m1A Human chr1 + 151458866 151458866 151458866 CGCCGGGGGGCGGGGGCGGCCGGCCAGCCGGCAGGCAGGGACCTCCGCCGCCGGCCCTTCGCGCG CGCCGGGGGGCGGGGGCGGCCGGCCAGCCGGCGGGCAGGGACCTCCGCCGCCGGCCCTTCGCGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151458853..151459067 26863196 MeRIP-seq:(Medium) rs1157424561 Functional Loss SNV dbSNP153 33..33 33 - - - 93613 RMVar_ID_93613 Human_SNP_ID_33671776 m1A Human chr1 - 151459069 151459069 151459069 TCCGTTATCTTTTCGCTCGGCGAGGCGTTCAGAGGCGAGACAATGAGAGGGGGATGGGGCCGGTA TCCGTTATCTTTTCGCTCGGCGAGGCGTTCAGCGGCGAGACAATGAGAGGGGGATGGGGCCGGTA T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151459064..151459208;chr1:151459064..151459162 26863196 MeRIP-seq:(Medium) rs1320775011 Functional Loss SNV dbSNP153 33..33 33 - - - 93614 RMVar_ID_93614 Human_SNP_ID_33689141 m1A Human chr1 + 151529996 151529996 151529996 TGGAGACGACGCTTCGGGAGACCCAGGAGGAAAATGACGAATTCCGCCGGCGCATCCTGGGTTTG TGGAGACGACGCTTCGGGAGACCCAGGAGGAAGATGACGAATTCCGCCGGCGCATCCTGGGTTTG A G CGN Ensembl:ENSG00000143375 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151529947..151530147 26863196 MeRIP-seq:(Medium) rs749713533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19739,RMVar_hsa_circ_367904 93615 RMVar_ID_93615 Human_SNP_ID_33689196 m1A Human chr1 - 151530117 151530117 151530117 GAGCAGAGAGGGCTGGGAGGGCAGAACCACTGACCTCCAGCCGCTGCAGCTTGTCCCGTAGTCGT GAGCAGAGAGGGCTGGGAGGGCAGAACCACTGCCCTCCAGCCGCTGCAGCTTGTCCCGTAGTCGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151530068..151530139 26863196 MeRIP-seq:(Medium) rs914543522 Functional Loss SNV dbSNP153 33..33 33 - - - 93616 RMVar_ID_93616 Human_SNP_ID_33690292 m1A Human chr1 + 151534093 151534093 151534093 GCAGGGGCTGGAGCAAGAGGCAGAGAACAAGAAGCGTTCCCAGGACGACAGGGCCCGGCAGCTGA GCAGGGGCTGGAGCAAGAGGCAGAGAACAAGAGGCGTTCCCAGGACGACAGGGCCCGGCAGCTGA A G CGN Ensembl:ENSG00000143375 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151533950..151534153 26863196 MeRIP-seq:(Medium) rs1553246988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_130123 RMVar_hsa_circ_19739,RMVar_hsa_circ_65997 93617 RMVar_ID_93617 Human_SNP_ID_33690512 m1A Human chr1 + 151535084 151535084 151535084 CACGGCTGGAAACAGAGTTAGATGAGGAGAAGAACACCGTGGAGCTGCTAACAGATCGGGTGAAT CACGGCTGGAAACAGAGTTAGATGAGGAGAAGGACACCGTGGAGCTGCTAACAGATCGGGTGAAT A G CGN Ensembl:ENSG00000143375 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151535067..151535146 26863196 MeRIP-seq:(Medium) rs1167999078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_130124,Human_Splice_Rec_130125,Human_Splice_Rec_130147 RMVar_hsa_circ_19739,RMVar_hsa_circ_65997 93618 RMVar_ID_93618 Human_SNP_ID_33691824 m1A Human chr1 - 151540428 151540428 151540428 AAACGGAGAAGACAGCGAGAGCGCTTTTTCTTACCGCCGCCTGGTCCTCTGGGTGCACGTCCACC AAACGGAGAAGACAGCGAGAGCGCTTTTTCTTTCCGCCGCCTGGTCCTCTGGGTGCACGTCCACC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr1:151540330..151540451;chr1:151540398..151540504 26863196,32194978 MeRIP-seq:(Medium) rs111671554 Functional Loss SNV dbSNP153 33..33 33 - - - 93619 RMVar_ID_93619 Human_SNP_ID_33691825 m1A Human chr1 - 151540428 151540428 151540428 AAACGGAGAAGACAGCGAGAGCGCTTTTTCTTACCGCCGCCTGGTCCTCTGGGTGCACGTCCACC AAACGGAGAAGACAGCGAGAGCGCTTTTTCTTGCCGCCGCCTGGTCCTCTGGGTGCACGTCCACC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr1:151540330..151540451;chr1:151540398..151540504 26863196,32194978 MeRIP-seq:(Medium) rs111671554 Functional Loss SNV dbSNP153 33..33 33 - - - 93620 RMVar_ID_93620 Human_SNP_ID_33696906 m1A Human chr1 + 151562051 151562050 151562051 TGTACTGGTAGCAGTTTGTACCTGTAGACTGTAAAGTTGAGGGGTTATTGTTGCTGTCATTGTCA TGTACTGGTAGCAGTTTGTACCTGTAGACTGT_AAGTTGAGGGGTTATTGTTGCTGTCATTGTCA TA T TUFT1 Ensembl:ENSG00000143367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151562049..151562156 26863196 MeRIP-seq:(Medium) rs1173547548 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_114052,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151,RMVar_hsa_circ_136140 93621 RMVar_ID_93621 Human_SNP_ID_33697366 m1A Human chr1 + 151563860 151563860 151563860 CACTATATGAAGCTGCCTATTTTTGTATAGTTAATTTAATTTGAGGTTTCTTAACTAAATGGTGT CACTATATGAAGCTGCCTATTTTTGTATAGTTGATTTAATTTGAGGTTTCTTAACTAAATGGTGT A G TUFT1 Ensembl:ENSG00000143367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151563858..151564000 26863196 MeRIP-seq:(Medium) rs1405463141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41192,RMVar_hsa_circ_110647,RMVar_hsa_circ_114052,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151,RMVar_hsa_circ_136140 93622 RMVar_ID_93622 Human_SNP_ID_33697519 m1A Human chr1 + 151564458 151564458 151564458 GACTCGCAGTACAGGCCAGGGATGGGGCACAGAGTTGGGTGAGTTGGCATGCTCTCTTTCTCTAC GACTCGCAGTACAGGCCAGGGATGGGGCACAGGGTTGGGTGAGTTGGCATGCTCTCTTTCTCTAC A G TUFT1 Ensembl:ENSG00000143367 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:151564456..151564545 26863196 MeRIP-seq:(Medium) rs373428303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41192,RMVar_hsa_circ_110647,RMVar_hsa_circ_114052,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151,RMVar_hsa_circ_136140,RMVar_hsa_circ_136142,RMVar_hsa_circ_310305 93623 RMVar_ID_93623 Human_SNP_ID_33699971 m1A Human chr1 + 151574352 151574352 151574352 TCAGAGAGAGGAGGACAGAGTGGAGCAGAAAGAGGCAGAAGTCGGAGAGCTGCAGAGGCGCTTGC TCAGAGAGAGGAGGACAGAGTGGAGCAGAAAGGGGCAGAAGTCGGAGAGCTGCAGAGGCGCTTGC A G TUFT1 Ensembl:ENSG00000143367 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:151574301..151575000 26863196 MeRIP-seq:(Medium) rs1247441433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_130170,Human_Splice_Rec_130171,Human_Splice_Rec_130192,Human_Splice_Rec_130193,Human_Splice_Rec_130216,Human_Splice_Rec_130217,Human_Splice_Rec_130238,Human_Splice_Rec_130258,Human_Splice_Rec_130259 RMVar_hsa_circ_110647,RMVar_hsa_circ_114052,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151,RMVar_hsa_circ_136140,RMVar_hsa_circ_64262,RMVar_hsa_circ_266855 93624 RMVar_ID_93624 Human_SNP_ID_33701547 m1A Human chr1 + 151580771 151580771 151580771 TTATGGAGGAGCAGGTATTGGAGGATAAGCGCAATCTATGGTAATGAAGATGAGGCAAGTGGGTA TTATGGAGGAGCAGGTATTGGAGGATAAGCGCGATCTATGGTAATGAAGATGAGGCAAGTGGGTA A G TUFT1 Ensembl:ENSG00000143367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151580766..151580914 26863196 MeRIP-seq:(Medium) rs1396443752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151 93625 RMVar_ID_93625 Human_SNP_ID_33701595 m1A Human chr1 + 151580963 151580963 151580963 TTGTGTTACAGAATTTAGAGATGCATGACCGGATGGAACACCTGATAGAAAAACAAATCAGTCAT TTGTGTTACAGAATTTAGAGATGCATGACCGGGTGGAACACCTGATAGAAAAACAAATCAGTCAT A G TUFT1 Ensembl:ENSG00000143367 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151580746..151580962 26863196 MeRIP-seq:(Medium) rs774041226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5690164,Human_RBP_ID_10581276 Human_Splice_Rec_130178,Human_Splice_Rec_130179,Human_Splice_Rec_130200,Human_Splice_Rec_130201,Human_Splice_Rec_130224,Human_Splice_Rec_130225 RMVar_hsa_circ_110647,RMVar_hsa_circ_136139,RMVar_hsa_circ_136141,RMVar_hsa_circ_99151 93626 RMVar_ID_93626 Human_SNP_ID_33701803 m1A Human chr1 + 151581761 151581761 151581761 CCATTGCTGCTGCCTCTGCCTCGGAGAAGCCCACTGCCCCTGTTGGCTGTTAACACTGCCTTTGA CCATTGCTGCTGCCTCTGCCTCGGAGAAGCCCGCTGCCCCTGTTGGCTGTTAACACTGCCTTTGA A G TUFT1 Ensembl:ENSG00000143367 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151581711..151581794 26863196 MeRIP-seq:(Medium) rs1263512977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23332664,Human_RBP_ID_27388235 Human_miRNA_ID_1010833,Human_miRNA_ID_1019052,Human_miRNA_ID_2456188,Human_miRNA_ID_2461098,Human_miRNA_ID_2633755,Human_miRNA_ID_2636442 RMVar_hsa_circ_136141,RMVar_hsa_circ_99151 93627 RMVar_ID_93627 Human_SNP_ID_33706292 m1A Human chr1 - 151600318 151600318 151600318 GGCAGAGGGTTTCCTCACTTCTCAGACGGGGCAGCCGGGCAGAGACGCTCCTCACCTCCCAGACA GGCAGAGGGTTTCCTCACTTCTCAGACGGGGCGGCCGGGCAGAGACGCTCCTCACCTCCCAGACA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:151600295..151600419 26863196 MeRIP-seq:(Medium) rs1407254743 Functional Loss SNV dbSNP153 33..33 33 - - - 93628 RMVar_ID_93628 Human_SNP_ID_33709316 m1A Human chr1 - 151612235 151612235 151612235 GCCGCCGCCACCTCCGTTCCTGTGAGGGGCTGAGGGATGAATCCCTTCCCCGTCCTCGTCCGCCA GCCGCCGCCACCTCCGTTCCTGTGAGGGGCTGCGGGATGAATCCCTTCCCCGTCCTCGTCCGCCA T G AL391335.1 Ensembl:ENSG00000250734 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:151612051..151612528 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 93629 RMVar_ID_93629 Human_SNP_ID_33745368 m1A Human chr1 - 151763059 151763059 151763059 AGCCGCGCCTGCACCGGCGACATCGCGTCTATAAGCTGGTGGAGGACACGAAGCATCGGCCCAAA AGCCGCGCCTGCACCGGCGACATCGCGTCTATGAGCTGGTGGAGGACACGAAGCATCGGCCCAAA T C MRPL9 Ensembl:ENSG00000143436 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:151762976..151763425 32194978 MeRIP-seq:(Medium) rs1442038806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_971300,Human_RBP_ID_3994333,Human_RBP_ID_8956136,Human_RBP_ID_27579000 Human_Splice_Rec_130702,Human_Splice_Rec_130703,Human_Splice_Rec_130714,Human_Splice_Rec_130730,Human_Splice_Rec_130731,Human_Splice_Rec_130742,Human_Splice_Rec_130743,Human_Splice_Rec_130754,Human_Splice_Rec_130763,Human_Splice_Rec_130772,Human_Splice_Rec_130773,Human_Splice_Rec_130780,Human_Splice_Rec_130781,Human_Splice_Rec_130784 93630 RMVar_ID_93630 Human_SNP_ID_33745520 m1A Human chr1 - 151763344 151763344 151763344 AAGGGAACGCCCCTGACCTGGCCTGCAACTTCAGCCTTTCTCAAAATCGGGTGAGGGCTGAGTCT AAGGGAACGCCCCTGACCTGGCCTGCAACTTCGGCCTTTCTCAAAATCGGGTGAGGGCTGAGTCT T C MRPL9 Ensembl:ENSG00000143436 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:151763326..151763500 26863196 MeRIP-seq:(Medium) rs1347414607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_971301,Human_RBP_ID_4081494,Human_RBP_ID_8285434 Human_Splice_Rec_130701,Human_Splice_Rec_130713,Human_Splice_Rec_130729,Human_Splice_Rec_130741,Human_Splice_Rec_130753,Human_Splice_Rec_130771,Human_Splice_Rec_130779,Human_Splice_Rec_130783 RMVar_hsa_circ_136169,RMVar_hsa_circ_377784 93631 RMVar_ID_93631 Human_SNP_ID_33745557 m1A Human chr1 + 151763403 151763403 151763403 TCCCTTCATGTCGCGGCCGCAGTAGCTCCTGGACGCCTCCCCGAAGCAGCCGTCCAGCGCCCGCC TCCCTTCATGTCGCGGCCGCAGTAGCTCCTGGCCGCCTCCCCGAAGCAGCCGTCCAGCGCCCGCC A C OAZ3 Ensembl:ENSG00000143450 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:151763040..151763510 26863410 MeRIP-seq:(Medium) rs768370611 Functional Loss SNV dbSNP153 33..33 33 - - - 93632 RMVar_ID_93632 Human_SNP_ID_33745583 m1A Human chr1 + 151763442 151763442 151763442 CCCGAAGCAGCCGTCCAGCGCCCGCCCGCAGCAGAGCTCTGCCCGGGGCCGTGACAACGGGCGCC CCCGAAGCAGCCGTCCAGCGCCCGCCCGCAGCGGAGCTCTGCCCGGGGCCGTGACAACGGGCGCC A G OAZ3 Ensembl:ENSG00000143450 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151763026..151763500 26863196 MeRIP-seq:(Medium) rs897185006 Functional Loss SNV dbSNP153 33..33 33 - - - 93633 RMVar_ID_93633 Human_SNP_ID_33745600 m1A Human chr1 - 151763461 151763461 151763461 CTGTGCCTGTGAACATGGCGGCGCCCGTTGTCACGGCCCCGGGCAGAGCTCTGCTGCGGGCGGGC CTGTGCCTGTGAACATGGCGGCGCCCGTTGTCCCGGCCCCGGGCAGAGCTCTGCTGCGGGCGGGC T G MRPL9,AL589765.4 Ensembl:ENSG00000143436,Ensembl:ENSG00000249602 Protein coding,lincRNA CDS,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151762948..151763515 26863196 MeRIP-seq:(Medium) rs768160583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074395,Human_RBP_ID_5161476,Human_RBP_ID_26798881,Human_RBP_ID_26841866 Human_Splice_Rec_130848 93634 RMVar_ID_93634 Human_SNP_ID_33750989 m1A Human chr1 - 151783051 151783051 151783051 AACCTCCCTCTTTTCCCTGCTTTGCTTGTTTCAGGATATAAGTCAAAGAGTACAGCAGAAAATGT AACCTCCCTCTTTTCCCTGCTTTGCTTGTTTCCGGATATAAGTCAAAGAGTACAGCAGAAAATGT T G TDRKH Ensembl:ENSG00000182134 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr1:151783005..151783099;chr1:151783001..151783121 26863196,26863410 MeRIP-seq:(Medium) rs754296502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136171,RMVar_hsa_circ_108927 93635 RMVar_ID_93635 Human_SNP_ID_33767747 m1A Human chr1 + 151851979 151851979 151851979 GCTTGATAGTTAGGGAGGGGCAGTCAGTGAGAAGTCGGGGCAGGAGCTGGGCTGGCTGTCCTCCA GCTTGATAGTTAGGGAGGGGCAGTCAGTGAGAGGTCGGGGCAGGAGCTGGGCTGGCTGTCCTCCA A G C2CD4D-AS1,C2CD4D-AS1:2,C2CD4D-AS1:3 RNACentral:URS00008BA739,RNACentral:URS00008BEC73,RNACentral:URS00008C2208 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:151851929..151852110 26863196 MeRIP-seq:(Medium) rs1296737734 Functional Loss SNV dbSNP153 33..33 33 - - - 93636 RMVar_ID_93636 Human_SNP_ID_33773170 m1A Human chr1 - 151874373 151874373 151874373 AAGAACCCATCTCAAACAAACAAACAAACAAAAAAAAAAAACTCTTGTCTCCTTAGGATATGTTA AAGAACCCATCTCAAACAAACAAACAAACAAACAAAAAAAACTCTTGTCTCCTTAGGATATGTTA T G THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3180671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27388283 Human_miRNA_ID_179613 93637 RMVar_ID_93637 Human_SNP_ID_33773235 m1A Human chr1 - 151874650 151874650 151874650 AACTCTCGGGCCAGGCGCTGTGGCTCACACCTATAATCCCAGCACTTTAGGAGGCCGAGGCAGGC AACTCTCGGGCCAGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGC T C THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12045899 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12194,GWAS_ID_12195,GWAS_ID_12196,GWAS_ID_12197,GWAS_ID_12198 93638 RMVar_ID_93638 Human_SNP_ID_33777894 m1A Human chr1 - 151894638 151894638 151894638 GGTTATATCACCCTAAGAAGCTTAGAACACTCAGGTTATACCCACATCTCCCAGTATCTAAATCC GGTTATATCACCCTAAGAAGCTTAGAACACTCCGGTTATACCCACATCTCCCAGTATCTAAATCC T G THEM4 Ensembl:ENSG00000159445 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:151894602..151894749 26863196 MeRIP-seq:(Medium) rs780845812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10582906 Human_miRNA_ID_2296749 RMVar_hsa_circ_369425,RMVar_hsa_circ_136175,RMVar_hsa_circ_104150,RMVar_hsa_circ_136177 93639 RMVar_ID_93639 Human_SNP_ID_33781379 m1A Human chr1 - 151909381 151909381 151909381 TGCCTGCCGCCAGTAGGCCGGCGCCTGCCGGGAAGCGAGCCGCGACCCGAGCTGGTGAGTCTGGG TGCCTGCCGCCAGTAGGCCGGCGCCTGCCGGGGAGCGAGCCGCGACCCGAGCTGGTGAGTCTGGG T C THEM4 Ensembl:ENSG00000159445 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151909374..151909474 26863196 MeRIP-seq:(Medium) rs1428025380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074397,Human_RBP_ID_22871396 Human_Splice_Rec_131219,Human_Splice_Rec_131229,Human_Splice_Rec_131253 93640 RMVar_ID_93640 Human_SNP_ID_33797718 m1A Human chr1 + 151983310 151983310 151983310 TCCAGGTCCTTCATTATTTTGTCCACAGCCAGAGGGTCTTTTTGATTCTGAAAAAAAAAAGAACA TCCAGGTCCTTCATTATTTTGTCCACAGCCAGGGGGTCTTTTTGATTCTGAAAAAAAAAAGAACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:151983262..151984115 32194978 MeRIP-seq:(Medium) rs749748438 Functional Loss SNV dbSNP153 33..33 33 - - - 93641 RMVar_ID_93641 Human_SNP_ID_33797721 m1A Human chr1 - 151983319 151983319 151983319 TCTTGCCTTTGTTCTTTTTTTTTTCAGAATCAAAAAGACCCTCTGGCTGTGGACAAAATAATGAA TCTTGCCTTTGTTCTTTTTTTTTTCAGAATCAGAAAGACCCTCTGGCTGTGGACAAAATAATGAA T C S100A10 Ensembl:ENSG00000197747 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:151983035..151983346;chr1:151982995..151983365;chr1:151983185..151983367 26863196 MeRIP-seq:(Medium) rs367809896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_131264,Human_Splice_Rec_131268,Human_Splice_Rec_131274 Human_miRNA_ID_2156832 RMVar_hsa_circ_80438,RMVar_hsa_circ_109261,RMVar_hsa_circ_95807,RMVar_hsa_circ_136178,RMVar_hsa_circ_136179,RMVar_hsa_circ_136180 93642 RMVar_ID_93642 Human_SNP_ID_33798354 m1A Human chr1 - 151986225 151986225 151986225 TAATAGGCTTCAACGGACCACACCAAAATGCCATCTCAAATGGAACACGCCATGGAAACCATGAT TAATAGGCTTCAACGGACCACACCAAAATGCCCTCTCAAATGGAACACGCCATGGAAACCATGAT T G S100A10 Ensembl:ENSG00000197747 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:151986176..151986275 26863196 MeRIP-seq:(Medium) rs776775873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326673,Human_RBP_ID_971311,Human_RBP_ID_4075949,Human_RBP_ID_5458535,Human_RBP_ID_17446214,Human_RBP_ID_18204515,Human_RBP_ID_27388298 Human_Splice_Rec_131262,Human_Splice_Rec_131266,Human_Splice_Rec_131270,Human_Splice_Rec_131276 RMVar_hsa_circ_109261,RMVar_hsa_circ_95807,RMVar_hsa_circ_136179,RMVar_hsa_circ_136180,RMVar_hsa_circ_64971 93643 RMVar_ID_93643 Human_SNP_ID_33800112 m1A Human chr1 - 151993793 151993768 151993793 GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCCAGCTCGCCCAGCTCGCCCAGCGTCCGCCGCGCC GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCC_________________________GCCGCGCC CGGACGCTGGGCGAGCTGGGCGAGCT C S100A10 Ensembl:ENSG00000197747 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151986065..151994091;chr1:151986049..151994125 26863196 MeRIP-seq:(Medium) rs1220671785 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_859024,Human_RBP_ID_3994419 Human_Splice_Rec_131261,Human_Splice_Rec_131269,Human_Splice_Rec_131275 RMVar_hsa_circ_109261,RMVar_hsa_circ_136180 93644 RMVar_ID_93644 Human_SNP_ID_33800124 m1A Human chr1 + 151993790 151993790 151993790 CGAGGCGCGGCGGACGCTGGGCGAGCTGGGCGAGCTGGACGCGGGGCGGAGAGGCGAGCGCGGCG CGAGGCGCGGCGGACGCTGGGCGAGCTGGGCGGGCTGGACGCGGGGCGGAGAGGCGAGCGCGGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:151986126..151993900 26863410 MeRIP-seq:(Medium) rs1276012519 Functional Loss SNV dbSNP153 33..33 33 - - - 93645 RMVar_ID_93645 Human_SNP_ID_33800126 m1A Human chr1 - 151993793 151993793 151993793 GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCCAGCTCGCCCAGCTCGCCCAGCGTCCGCCGCGCC GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCCTGCTCGCCCAGCTCGCCCAGCGTCCGCCGCGCC T A S100A10 Ensembl:ENSG00000197747 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151986065..151994091;chr1:151986049..151994125 26863196 MeRIP-seq:(Medium) rs976825746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_859024,Human_RBP_ID_3994419 Human_Splice_Rec_131261,Human_Splice_Rec_131269,Human_Splice_Rec_131275 RMVar_hsa_circ_109261,RMVar_hsa_circ_136180 93646 RMVar_ID_93646 Human_SNP_ID_33800127 m1A Human chr1 - 151993793 151993793 151993793 GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCCAGCTCGCCCAGCTCGCCCAGCGTCCGCCGCGCC GCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCCCGCTCGCCCAGCTCGCCCAGCGTCCGCCGCGCC T G S100A10 Ensembl:ENSG00000197747 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:151986065..151994091;chr1:151986049..151994125 26863196 MeRIP-seq:(Medium) rs976825746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_859024,Human_RBP_ID_3994419 Human_Splice_Rec_131261,Human_Splice_Rec_131269,Human_Splice_Rec_131275 RMVar_hsa_circ_109261,RMVar_hsa_circ_136180 93647 RMVar_ID_93647 Human_SNP_ID_33800128 m1A Human chr1 + 151993796 151993796 151993796 GCGGCGGACGCTGGGCGAGCTGGGCGAGCTGGACGCGGGGCGGAGAGGCGAGCGCGGCGGGCTGT GCGGCGGACGCTGGGCGAGCTGGGCGAGCTGGCCGCGGGGCGGAGAGGCGAGCGCGGCGGGCTGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:151986249..151993843 32194978 MeRIP-seq:(Medium) rs1228004892 Functional Loss SNV dbSNP153 33..33 33 - - - 93648 RMVar_ID_93648 Human_SNP_ID_33800139 m1A Human chr1 - 151993826 151993826 151993826 CCCACCCGCCGCACGTACTAAGGAAGGCGCACAGCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCC CCCACCCGCCGCACGTACTAAGGAAGGCGCACGGCCCGCCGCGCTCGCCTCTCCGCCCCGCGTCC T C S100A10 Ensembl:ENSG00000197747 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:151986249..151993843 26863410 MeRIP-seq:(Medium) rs557824954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_131261,Human_Splice_Rec_131269,Human_Splice_Rec_131275 RMVar_hsa_circ_109261,RMVar_hsa_circ_136180 93649 RMVar_ID_93649 Human_SNP_ID_33808639 m1A Human chr1 - 152032573 152032573 152032573 TCATCTCCACAGCCCACCCATCCCCTGAGCACACTAACCACCTCATGCAGGCCCCACCTGCCAAT TCATCTCCACAGCCCACCCATCCCCTGAGCACGCTAACCACCTCATGCAGGCCCCACCTGCCAAT T C S100A11 Ensembl:ENSG00000163191 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:152032501..152032700 26863196 MeRIP-seq:(Medium) rs1290505720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326678,Human_RBP_ID_743986,Human_RBP_ID_17212476,Human_RBP_ID_17338425,Human_RBP_ID_17647654,Human_RBP_ID_18928593,Human_RBP_ID_19151494,Human_RBP_ID_24455192,Human_RBP_ID_26841892,Human_RBP_ID_27168264,Human_RBP_ID_27388301 Human_miRNA_ID_623138 RMVar_hsa_circ_104799,RMVar_hsa_circ_121205,RMVar_hsa_circ_136182,RMVar_hsa_circ_83952,RMVar_hsa_circ_136183,RMVar_hsa_circ_136181 93650 RMVar_ID_93650 Human_SNP_ID_33808641 m1A Human chr1 - 152032603 152032600 152032603 CCACCCCCTTTCCTTCCAGCCTTTCTGTCATCATCTCCACAGCCCACCCATCCCCTGAGCACACT CCACCCCCTTTCCTTCCAGCCTTTCTGTCATC___TCCACAGCCCACCCATCCCCTGAGCACACT AGAT A S100A11 Ensembl:ENSG00000163191 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:152032553..152032727 26863196 MeRIP-seq:(Medium) rs1373282368 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_22762,Human_RBP_ID_326678,Human_RBP_ID_743986,Human_RBP_ID_8285463,Human_RBP_ID_17221623,Human_RBP_ID_17338426,Human_RBP_ID_17647654,Human_RBP_ID_18928593,Human_RBP_ID_24447318,Human_RBP_ID_27388302 Human_miRNA_ID_132910,Human_miRNA_ID_299845,Human_miRNA_ID_1381059,Human_miRNA_ID_1983764,Human_miRNA_ID_2064249,Human_miRNA_ID_2702126,Human_miRNA_ID_2872391,Human_miRNA_ID_2933430,Human_miRNA_ID_2939401,Human_miRNA_ID_2980357 RMVar_hsa_circ_104799,RMVar_hsa_circ_121205,RMVar_hsa_circ_136182,RMVar_hsa_circ_83952,RMVar_hsa_circ_136183,RMVar_hsa_circ_136181 93651 RMVar_ID_93651 Human_SNP_ID_33808645 m1A Human chr1 + 152032614 152032614 152032614 GGGATGGGTGGGCTGTGGAGATGATGACAGAAAGGCTGGAAGGAAAGGGGGTGGGTTTGAAGGCC GGGATGGGTGGGCTGTGGAGATGATGACAGAAGGGCTGGAAGGAAAGGGGGTGGGTTTGAAGGCC A G AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:152032565..152032717 26863196 MeRIP-seq:(Medium) rs1048411966 Functional Loss SNV dbSNP153 33..33 33 - - - 93652 RMVar_ID_93652 Human_SNP_ID_33809612 m1A Human chr1 + 152036953 152036953 152036953 AGCTGAGCGAGGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGAGAGCTCTGTGCGCGCGGCGTGC AGCTGAGCGAGGCGCGGGAGGCTGTGGCTGGGGGCGGCGCTGAGAGCTCTGTGCGCGCGGCGTGC A G AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972531,GSM1972532 HEK293T,untreat control;HEPG2 cell line,mRNA heat shock 4h chr1:152033766..152036975;chr1:152033586..152037025 26863410,26863196 MeRIP-seq:(Medium) rs753704548 Functional Loss SNV dbSNP153 33..33 33 - - - 93653 RMVar_ID_93653 Human_SNP_ID_33809615 m1A Human chr1 - 152036961 152036961 152036961 CCAGACCCGCACGCCGCGCGCACAGAGCTCTCAGCGCCGCTCCCAGCCACAGCCTCCCGCGCCTC CCAGACCCGCACGCCGCGCGCACAGAGCTCTCGGCGCCGCTCCCAGCCACAGCCTCCCGCGCCTC T C S100A11 Ensembl:ENSG00000163191 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:152033602..152037025;chr1:152033626..152037025 31548705,26863196 m1A-IP-seq:(High) rs1395370296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22767,Human_RBP_ID_3994442,Human_RBP_ID_8240180 Human_Splice_Rec_131303 Human_miRNA_ID_1355008 RMVar_hsa_circ_93683,RMVar_hsa_circ_83952,RMVar_hsa_circ_136181,RMVar_hsa_circ_136185 93654 RMVar_ID_93654 Human_SNP_ID_33809616 m1A Human chr1 + 152036963 152036963 152036963 GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGAGAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGCGAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG A C AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:152036818..152037025;chr1:152036870..152037025 26863196 MeRIP-seq:(Medium) rs745398370 Functional Loss SNV dbSNP153 33..33 33 - - - 93655 RMVar_ID_93655 Human_SNP_ID_33809617 m1A Human chr1 + 152036963 152036963 152036963 GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGAGAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGGGAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG A G AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:152036818..152037025;chr1:152036870..152037025 26863196 MeRIP-seq:(Medium) rs745398370 Functional Loss SNV dbSNP153 33..33 33 - - - 93656 RMVar_ID_93656 Human_SNP_ID_34203671 m1A Human chr1 - 153534829 153534829 153534829 TGAGTATGGATTTCACATTCTAACACATTAGAAGCTGCAGGATGCTGAAATTGCAAGGCTGATGG TGAGTATGGATTTCACATTCTAACACATTAGAGGCTGCAGGATGCTGAAATTGCAAGGCTGATGG T C S100A6 Ensembl:ENSG00000197956 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153534626..153534850 32194978 MeRIP-seq:(Medium) rs749958198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_131698,Human_Splice_Rec_131702,Human_Splice_Rec_131706,Human_Splice_Rec_131708 Human_miRNA_ID_2011187,Human_miRNA_ID_2757539 RMVar_hsa_circ_93996,RMVar_hsa_circ_104305,RMVar_hsa_circ_99399,RMVar_hsa_circ_136205,RMVar_hsa_circ_136206,RMVar_hsa_circ_136204 93657 RMVar_ID_93657 Human_SNP_ID_34206204 m1A Human chr1 - 153543872 153543870 153543872 CTTTCCAGAAGCTGATGAGCAACTTGGACAGCAACAGGGACAACGAGGTGGACTTCCAAGAGTAC CTTTCCAGAAGCTGATGAGCAACTTGGACAGC__CAGGGACAACGAGGTGGACTTCCAAGAGTAC GTT G S100A4 Ensembl:ENSG00000196154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153543674..153543956 26863196 MeRIP-seq:(Medium) rs763415081 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24447343 Human_Splice_Rec_131724,Human_Splice_Rec_131726,Human_Splice_Rec_131732,Human_Splice_Rec_131736,Human_Splice_Rec_131740,Human_Splice_Rec_131744 RMVar_hsa_circ_106855,RMVar_hsa_circ_122775,RMVar_hsa_circ_136208,RMVar_hsa_circ_136209 93658 RMVar_ID_93658 Human_SNP_ID_34206412 m1A Human chr1 - 153544696 153544696 153544696 GAGGGTGACAAGTTCAAGCTCAACAAGTCAGAACTAAAGGAGCTGCTGACCCGGGAGCTGCCCAG GAGGGTGACAAGTTCAAGCTCAACAAGTCAGAGCTAAAGGAGCTGCTGACCCGGGAGCTGCCCAG T C S100A4 Ensembl:ENSG00000196154 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1050923 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_131723,Human_Splice_Rec_131725,Human_Splice_Rec_131731,Human_Splice_Rec_131735,Human_Splice_Rec_131739,Human_Splice_Rec_131743 RMVar_hsa_circ_106855,RMVar_hsa_circ_122775,RMVar_hsa_circ_136208,RMVar_hsa_circ_136209,RMVar_hsa_circ_116803,RMVar_hsa_circ_136210 93659 RMVar_ID_93659 Human_SNP_ID_34206452 m1A Human chr1 - 153544803 153544803 153544803 ACGGTCTCTGTGCCTCCTGCTCCCAGATCCTGACTGCTGTCATGGCGTGCCCTCTGGAGAAGGCC ACGGTCTCTGTGCCTCCTGCTCCCAGATCCTGGCTGCTGTCATGGCGTGCCCTCTGGAGAAGGCC T C S100A4 Ensembl:ENSG00000196154 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:153544724..153544878;chr1:153544651..153544842;chr1:153544611..153544875;chr1:153544610..153544863 26863196 MeRIP-seq:(Medium) rs763849889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074407,Human_RBP_ID_22429672,Human_RBP_ID_24447346,Human_RBP_ID_26368602 Human_Splice_Rec_131722,Human_Splice_Rec_131730,Human_Splice_Rec_131734,Human_Splice_Rec_131738,Human_Splice_Rec_131742 RMVar_hsa_circ_106855,RMVar_hsa_circ_122775,RMVar_hsa_circ_136208,RMVar_hsa_circ_136209,RMVar_hsa_circ_116803,RMVar_hsa_circ_136210 93660 RMVar_ID_93660 Human_SNP_ID_34207197 m1A Human chr1 - 153547794 153547794 153547794 CTACAACAAATTCATGAGTGTTCTGGACACCAACAAGGACTGCGAGGTGGACTTTGTGGAGTATG CTACAACAAATTCATGAGTGTTCTGGACACCAGCAAGGACTGCGAGGTGGACTTTGTGGAGTATG T C S100A3,S100A4 Ensembl:ENSG00000188015,Ensembl:ENSG00000196154 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153547743..153547868 26863196 MeRIP-seq:(Medium) rs536309763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_131748,Human_Splice_Rec_131752 RMVar_hsa_circ_81060,RMVar_hsa_circ_136211 93661 RMVar_ID_93661 Human_SNP_ID_34208054 m1A Human chr1 - 153551293 153551293 153551293 GCAGGAAGGCTTCTTTGCCGGCCTGGGAGTCAATCTCCTTCCTCTTTTCCCTCTCACGCTCTTCT GCAGGAAGGCTTCTTTGCCGGCCTGGGAGTCAGTCTCCTTCCTCTTTTCCCTCTCACGCTCTTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153551227..153551661 26863196 MeRIP-seq:(Medium) rs1207804380 Functional Loss SNV dbSNP153 33..33 33 - - - 93662 RMVar_ID_93662 Human_SNP_ID_34208103 m1A Human chr1 + 153551480 153551480 153551480 TAGAGGAGGGAAGGAAAAGAGGAGCTGTGATTAGCCCTGTTTTATAATGGGCTACATAGCCCTGT TAGAGGAGGGAAGGAAAAGAGGAGCTGTGATTCGCCCTGTTTTATAATGGGCTACATAGCCCTGT A C LOC101928034,LOC101928034:2 RNACentral:URS00007E39B3,RNACentral:URS0000EC013C lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:153551460..153551636;chr1:153551449..153551643 26863196 MeRIP-seq:(Medium) rs553170976 Functional Loss SNV dbSNP153 33..33 33 - - - 93663 RMVar_ID_93663 Human_SNP_ID_34211204 m1A Human chr1 - 153563784 153563784 153563784 CCTGCCAAGAGGGCGACAAGTTCAAGCTGAGTAAGGGGGAAATGAAGGAACTTCTGCACAAGGAG CCTGCCAAGAGGGCGACAAGTTCAAGCTGAGTGAGGGGGAAATGAAGGAACTTCTGCACAAGGAG T C S100A2 Ensembl:ENSG00000196754 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153563517..153563862 26863196 MeRIP-seq:(Medium) rs1245905726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8285522 Human_Splice_Rec_131755,Human_Splice_Rec_131757,Human_Splice_Rec_131760,Human_Splice_Rec_131761,Human_Splice_Rec_131765,Human_Splice_Rec_131769,Human_Splice_Rec_131773 Human_miRNA_ID_2194256 RMVar_hsa_circ_101687,RMVar_hsa_circ_95455,RMVar_hsa_circ_136214,RMVar_hsa_circ_81760,RMVar_hsa_circ_136213,RMVar_hsa_circ_136215 93664 RMVar_ID_93664 Human_SNP_ID_34222889 m1A Human chr1 + 153608148 153608146 153608149 GACTGCCTTCTCCAGCTCCGTGTAGCAGTCTGACATCTCCCTGCTTCGCCTGCTGGCGGGGCCTG GACTGCCTTCTCCAGCTCCGTGTAGCAGTCT___ATCTCCCTGCTTCGCCTGCTGGCGGGGCCTG TGAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153608097..153608211 26863196 MeRIP-seq:(Medium) rs1380469768 Functional Loss DEL dbSNP153 32..34 33 - - - 93665 RMVar_ID_93665 Human_SNP_ID_34225790 m1A Human chr1 - 153618899 153618898 153618899 CAGGAAGAAGAAAGACCTGAAGATCAGGAAGAAGTAAAGCCGCCTGGCTGAGATGGGGTGGGCAG CAGGAAGAAGAAAGACCTGAAGATCAGGAAGA_GTAAAGCCGCCTGGCTGAGATGGGGTGGGCAG CT C S100A13 Ensembl:ENSG00000189171 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153618848..153618964 26863196 MeRIP-seq:(Medium) rs1205557070 Functional Loss DEL dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_326729,Human_RBP_ID_1725685,Human_RBP_ID_5136849,Human_RBP_ID_8956195,Human_RBP_ID_17647059,Human_RBP_ID_17725966,Human_RBP_ID_22430936,Human_RBP_ID_22637472,Human_RBP_ID_26311816 93666 RMVar_ID_93666 Human_SNP_ID_34225798 m1A Human chr1 - 153618926 153618926 153618926 ATTGATTGGGGAGCTGGCCAAGGAAATCAGGAAGAAGAAAGACCTGAAGATCAGGAAGAAGTAAA ATTGATTGGGGAGCTGGCCAAGGAAATCAGGAGGAAGAAAGACCTGAAGATCAGGAAGAAGTAAA T C S100A13 Ensembl:ENSG00000189171 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153618876..153619025 32194978 MeRIP-seq:(Medium) rs748899362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326730,Human_RBP_ID_855227,Human_RBP_ID_1725685,Human_RBP_ID_3994694,Human_RBP_ID_5136849,Human_RBP_ID_9356823,Human_RBP_ID_17647060,Human_RBP_ID_17725966,Human_RBP_ID_22023821,Human_RBP_ID_26311816 93667 RMVar_ID_93667 Human_SNP_ID_34229871 m1A Human chr1 + 153634129 153634129 153634129 GGAGCTGGCGGCCGCTGCAGACGAAAGGCAGGAAAGGGCAGGCCGGGTGAGCAGACGGATCGGCC GGAGCTGGCGGCCGCTGCAGACGAAAGGCAGGCAAGGGCAGGCCGGGTGAGCAGACGGATCGGCC A C CHTOP Ensembl:ENSG00000160679 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:153634076..153634250 26863196 MeRIP-seq:(Medium) rs976115049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222589,Human_RBP_ID_743686,Human_RBP_ID_801942,Human_RBP_ID_858237,Human_RBP_ID_4074417,Human_RBP_ID_8285529,Human_RBP_ID_18551725,Human_RBP_ID_22025345 Human_miRNA_ID_3114850 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 93668 RMVar_ID_93668 Human_SNP_ID_34229873 m1A Human chr1 + 153634136 153634136 153634136 GCGGCCGCTGCAGACGAAAGGCAGGAAAGGGCAGGCCGGGTGAGCAGACGGATCGGCCGACTAGA GCGGCCGCTGCAGACGAAAGGCAGGAAAGGGCCGGCCGGGTGAGCAGACGGATCGGCCGACTAGA A C CHTOP Ensembl:ENSG00000160679 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153634051..153634667 26863196 MeRIP-seq:(Medium) rs1365655690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222589,Human_RBP_ID_743686,Human_RBP_ID_801942,Human_RBP_ID_858237,Human_RBP_ID_4074417,Human_RBP_ID_5691048,Human_RBP_ID_8285529,Human_RBP_ID_18551725,Human_RBP_ID_22025345 Human_miRNA_ID_3114850 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 93669 RMVar_ID_93669 Human_SNP_ID_34229904 m1A Human chr1 + 153634240 153634240 153634240 GCTTACGCATCTAACCAACCGCCCATCTAGCTAACCCGAGCCCCTCCACCGTCAACTCAGGTTCG GCTTACGCATCTAACCAACCGCCCATCTAGCTGACCCGAGCCCCTCCACCGTCAACTCAGGTTCG A G CHTOP Ensembl:ENSG00000160679 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153634076..153634360 26863196 MeRIP-seq:(Medium) rs978251656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743688,Human_RBP_ID_858238,Human_RBP_ID_5414464,Human_RBP_ID_5432905,Human_RBP_ID_5519173,Human_RBP_ID_8285531,Human_RBP_ID_17725971,Human_RBP_ID_22427512,Human_RBP_ID_26841924 Human_miRNA_ID_2389293,Human_miRNA_ID_2590518 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 93670 RMVar_ID_93670 Human_SNP_ID_34231107 m1A Human chr1 + 153638025 153638025 153638025 CTCTTGTCATATCTGCTTATTGCGTGTTTTTCATACCTTCCACCTCTCTAAAAGCCGTTACCTGA CTCTTGTCATATCTGCTTATTGCGTGTTTTTCCTACCTTCCACCTCTCTAAAAGCCGTTACCTGA A C CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153638001..153638025 26863196 MeRIP-seq:(Medium) rs906604340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271840,Human_RBP_ID_971326,Human_RBP_ID_1149624,Human_RBP_ID_3281632,Human_RBP_ID_5484392,Human_RBP_ID_5519930,Human_RBP_ID_5691093,Human_RBP_ID_17330368,Human_RBP_ID_17725987,Human_RBP_ID_19193065,Human_RBP_ID_27579030 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326,RMVar_hsa_circ_118301,RMVar_hsa_circ_136224 93671 RMVar_ID_93671 Human_SNP_ID_34231108 m1A Human chr1 + 153638025 153638025 153638025 CTCTTGTCATATCTGCTTATTGCGTGTTTTTCATACCTTCCACCTCTCTAAAAGCCGTTACCTGA CTCTTGTCATATCTGCTTATTGCGTGTTTTTCGTACCTTCCACCTCTCTAAAAGCCGTTACCTGA A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153638001..153638025 26863196 MeRIP-seq:(Medium) rs906604340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271840,Human_RBP_ID_971326,Human_RBP_ID_1149624,Human_RBP_ID_3281632,Human_RBP_ID_5484392,Human_RBP_ID_5519930,Human_RBP_ID_5691093,Human_RBP_ID_17330368,Human_RBP_ID_17725987,Human_RBP_ID_19193065,Human_RBP_ID_27579030 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326,RMVar_hsa_circ_118301,RMVar_hsa_circ_136224 93672 RMVar_ID_93672 Human_SNP_ID_34232931 m1A Human chr1 - 153645134 153645134 153645134 TGCTCCTTGGTCAATACAGGGCGAGCAAGGGCACCTCTCCCTCGTCCACGGCCTCGGCCTCGGCC TGCTCCTTGGTCAATACAGGGCGAGCAAGGGCGCCTCTCCCTCGTCCACGGCCTCGGCCTCGGCC T C lnc-S100A13-1 RNACentral:URS00008B8491 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:153645051..153645175 26863196 MeRIP-seq:(Medium) rs1455731990 Functional Loss SNV dbSNP153 33..33 33 - - - 93673 RMVar_ID_93673 Human_SNP_ID_34236640 m1A Human chr1 - 153658769 153658766 153658770 TGGGCCCCGCCACCGGGGTCCCTGCCCCCGATACAGCGGCGGAACCAGCCCCCGCCATCACGAAT TGGGCCCCGCCACCGGGGTCCCTGCCCCCGA____GCGGCGGAACCAGCCCCCGCCATCACGAAT CTGTA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153658726..153658828 26863196 MeRIP-seq:(Medium) rs1282551795 Functional Loss DEL dbSNP153 32..35 33 - - - 93674 RMVar_ID_93674 Human_SNP_ID_34236641 m1A Human chr1 - 153658769 153658769 153658769 TGGGCCCCGCCACCGGGGTCCCTGCCCCCGATACAGCGGCGGAACCAGCCCCCGCCATCACGAAT TGGGCCCCGCCACCGGGGTCCCTGCCCCCGATTCAGCGGCGGAACCAGCCCCCGCCATCACGAAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153658726..153658828 26863196 MeRIP-seq:(Medium) rs577300238 Functional Loss SNV dbSNP153 33..33 33 - - - 93675 RMVar_ID_93675 Human_SNP_ID_34236642 m1A Human chr1 - 153658769 153658769 153658769 TGGGCCCCGCCACCGGGGTCCCTGCCCCCGATACAGCGGCGGAACCAGCCCCCGCCATCACGAAT TGGGCCCCGCCACCGGGGTCCCTGCCCCCGATGCAGCGGCGGAACCAGCCCCCGCCATCACGAAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153658726..153658828 26863196 MeRIP-seq:(Medium) rs577300238 Functional Loss SNV dbSNP153 33..33 33 - - - 93676 RMVar_ID_93676 Human_SNP_ID_34237481 m1A Human chr1 + 153661327 153661327 153661327 CAAATAACAGATGAGCCTATGGACTCAGTAGCACAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC CAAATAACAGATGAGCCTATGGACTCAGTAGCCCAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC A C SNAPIN Ensembl:ENSG00000143553 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153661281..153661432 32194978 MeRIP-seq:(Medium) rs16835489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326805,Human_RBP_ID_10583756,Human_RBP_ID_22127952 Human_miRNA_ID_623319 93677 RMVar_ID_93677 Human_SNP_ID_34237482 m1A Human chr1 + 153661327 153661327 153661327 CAAATAACAGATGAGCCTATGGACTCAGTAGCACAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC CAAATAACAGATGAGCCTATGGACTCAGTAGCGCAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC A G SNAPIN Ensembl:ENSG00000143553 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153661281..153661432 32194978 MeRIP-seq:(Medium) rs16835489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326805,Human_RBP_ID_10583756,Human_RBP_ID_22127952 Human_miRNA_ID_623319 93678 RMVar_ID_93678 Human_SNP_ID_34237814 m1A Human chr1 - 153662454 153662452 153662455 ACCAGAGAAGAAGGAAGGAGAGGAAGAAGAGGAGAATACAGAAGAACCACCTCAAGGAGAGGAAG ACCAGAGAAGAAGGAAGGAGAGGAAGAAGAG___AATACAGAAGAACCACCTCAAGGAGAGGAAG TCTC T ILF2 Ensembl:ENSG00000143621 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153662404..153662492 26863196 MeRIP-seq:(Medium) rs756474490 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_803261,Human_RBP_ID_859375,Human_RBP_ID_1412125,Human_RBP_ID_1725769,Human_RBP_ID_4081622,Human_RBP_ID_5691361,Human_RBP_ID_8285620,Human_RBP_ID_9356828,Human_RBP_ID_10583793,Human_RBP_ID_17646537,Human_RBP_ID_17726043,Human_RBP_ID_18522600,Human_RBP_ID_18965965,Human_RBP_ID_22430947,Human_RBP_ID_22780101,Human_RBP_ID_22871397,Human_RBP_ID_23255566,Human_RBP_ID_24541218,Human_RBP_ID_24752145,Human_RBP_ID_26311820,Human_RBP_ID_26842008,Human_RBP_ID_27168360,Human_RBP_ID_27800785 RMVar_hsa_circ_136227,RMVar_hsa_circ_104995,RMVar_hsa_circ_118387,RMVar_hsa_circ_122948,RMVar_hsa_circ_126664,RMVar_hsa_circ_120297,RMVar_hsa_circ_110566,RMVar_hsa_circ_94334,RMVar_hsa_circ_95774,RMVar_hsa_circ_98310,RMVar_hsa_circ_94614,RMVar_hsa_circ_136231,RMVar_hsa_circ_136235,RMVar_hsa_circ_76039,RMVar_hsa_circ_84560,RMVar_hsa_circ_136236,RMVar_hsa_circ_136237,RMVar_hsa_circ_136233,RMVar_hsa_circ_136234,RMVar_hsa_circ_136232,RMVar_hsa_circ_136229,RMVar_hsa_circ_136230,RMVar_hsa_circ_136228,RMVar_hsa_circ_136226 93679 RMVar_ID_93679 Human_SNP_ID_34239678 m1A Human chr1 + 153669839 153669839 153669839 AATGTGTATCATTAACCCAAGGTACTCACCAAATAGAAGTCAAATGGGATATGTGGTACAAAGGG AATGTGTATCATTAACCCAAGGTACTCACCAAGTAGAAGTCAAATGGGATATGTGGTACAAAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:153669826..153669900 26863196 MeRIP-seq:(Medium) rs886682785 Functional Loss SNV dbSNP153 33..33 33 - - - 93680 RMVar_ID_93680 Human_SNP_ID_34239686 m1A Human chr1 + 153669881 153669881 153669881 AATGGGATATGTGGTACAAAGGGCCTGAACCTAAAACATGAAAAACAGCCAAATTATTCCCTAGG AATGGGATATGTGGTACAAAGGGCCTGAACCTGAAACATGAAAAACAGCCAAATTATTCCCTAGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153669876..153669900 26863196 MeRIP-seq:(Medium) rs375405198 Functional Loss SNV dbSNP153 33..33 33 - - - 93681 RMVar_ID_93681 Human_SNP_ID_34239981 m1A Human chr1 + 153670931 153670931 153670931 ACCGCTTCGACCCACTTACCTCATGGCGCCTTAAAACACGAACAATGGAGGCCGCACCAACCGCC ACCGCTTCGACCCACTTACCTCATGGCGCCTTCAAACACGAACAATGGAGGCCGCACCAACCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153668526..153671000 26863196 MeRIP-seq:(Medium) rs768198219 Functional Loss SNV dbSNP153 33..33 33 - - - 93682 RMVar_ID_93682 Human_SNP_ID_34239982 m1A Human chr1 + 153670931 153670931 153670931 ACCGCTTCGACCCACTTACCTCATGGCGCCTTAAAACACGAACAATGGAGGCCGCACCAACCGCC ACCGCTTCGACCCACTTACCTCATGGCGCCTTGAAACACGAACAATGGAGGCCGCACCAACCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153668526..153671000 26863196 MeRIP-seq:(Medium) rs768198219 Functional Loss SNV dbSNP153 33..33 33 - - - 93683 RMVar_ID_93683 Human_SNP_ID_34240197 m1A Human chr1 + 153671306 153671306 153671306 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTATCGGAGTTTTTTCATTG GCTGGGCCCATAACCCAGAGGTCGATGGATCGGAACCATCCTCTGCTATCGGAGTTTTTTCATTG A G tRNA-iMet-CAT-1-1,TRX-CAT1-1 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC tRNA,tRNA intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs748033005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269093,Human_RBP_ID_326870,Human_RBP_ID_1149648,Human_RBP_ID_1250275,Human_RBP_ID_1412178,Human_RBP_ID_1725800,Human_RBP_ID_3281709,Human_RBP_ID_4081659,Human_RBP_ID_5252820,Human_RBP_ID_5273226,Human_RBP_ID_5412983,Human_RBP_ID_5432915,Human_RBP_ID_5456334,Human_RBP_ID_5484402,Human_RBP_ID_5691402,Human_RBP_ID_8240188,Human_RBP_ID_8285646,Human_RBP_ID_8735114,Human_RBP_ID_8956229,Human_RBP_ID_9457760,Human_RBP_ID_10584062,Human_RBP_ID_16979218,Human_RBP_ID_17330393,Human_RBP_ID_17675122,Human_RBP_ID_17726061,Human_RBP_ID_18174106,Human_RBP_ID_18204531,Human_RBP_ID_18217198,Human_RBP_ID_18428563,Human_RBP_ID_18508611,Human_RBP_ID_18551837,Human_RBP_ID_19193290,Human_RBP_ID_22016009,Human_RBP_ID_22127986,Human_RBP_ID_22780119,Human_RBP_ID_22847098,Human_RBP_ID_23121415,Human_RBP_ID_23144365,Human_RBP_ID_23333275,Human_RBP_ID_24400664,Human_RBP_ID_24455052,Human_RBP_ID_24589116,Human_RBP_ID_26578309,Human_RBP_ID_26747263,Human_RBP_ID_26842036,Human_RBP_ID_27168387,Human_RBP_ID_27388394,Human_RBP_ID_27554391,Human_RBP_ID_27579068 93684 RMVar_ID_93684 Human_SNP_ID_34240262 m1A Human chr1 + 153671401 153671401 153671401 TTAGTGAAGGAAAATATCTTGCCAATTTTCCTACCTCAAAAATGCAACCAATATCAGCTATTTTT TTAGTGAAGGAAAATATCTTGCCAATTTTCCTGCCTCAAAAATGCAACCAATATCAGCTATTTTT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153671288..153671425 26863196 MeRIP-seq:(Medium) rs1181965768 Functional Loss SNV dbSNP153 33..33 33 - - - 93685 RMVar_ID_93685 Human_SNP_ID_34242110 m1A Human chr1 + 153678714 153678714 153678714 TCTGGCACACTCCCTGGGGCAGGCGCTCACGCACGCTACAAACACACACTCCTCTTTCCTCCCTC TCTGGCACACTCCCTGGGGCAGGCGCTCACGCGCGCTACAAACACACACTCCTCTTTCCTCCCTC A G NPR1 Ensembl:ENSG00000169418 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153678671..153678930 26863196 MeRIP-seq:(Medium) rs1221831378 Functional Loss SNV dbSNP153 33..33 33 - - - 93686 RMVar_ID_93686 Human_SNP_ID_34256586 m1A Human chr1 - 153728697 153728697 153728697 CCTGGGGCTCCTGCTCCCGCTCCTCCTCCTCCACCTCCCGCTGCTCCCGAAGCAGCTGCTGCTGC CCTGGGGCTCCTGCTCCCGCTCCTCCTCCTCCCCCTCCCGCTGCTCCCGAAGCAGCTGCTGCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153728648..153728748 26863196 MeRIP-seq:(Medium) rs1557982839 Functional Loss SNV dbSNP153 33..33 33 - - - 93687 RMVar_ID_93687 Human_SNP_ID_34259805 m1A Human chr1 - 153741332 153741332 153741332 TGGGCTTGGGCAGGTTCAGTGAGGATGAGAGTAAACAGGCCCAGGCAGATTTCTTCATGCTGGGG TGGGCTTGGGCAGGTTCAGTGAGGATGAGAGTGAACAGGCCCAGGCAGATTTCTTCATGCTGGGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153740732..153746971 32194978 MeRIP-seq:(Medium) rs938377124 Functional Loss SNV dbSNP153 33..33 33 - - - 93688 RMVar_ID_93688 Human_SNP_ID_34259806 m1A Human chr1 - 153741332 153741332 153741332 TGGGCTTGGGCAGGTTCAGTGAGGATGAGAGTAAACAGGCCCAGGCAGATTTCTTCATGCTGGGG TGGGCTTGGGCAGGTTCAGTGAGGATGAGAGTCAACAGGCCCAGGCAGATTTCTTCATGCTGGGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153740732..153746971 32194978 MeRIP-seq:(Medium) rs938377124 Functional Loss SNV dbSNP153 33..33 33 - - - 93689 RMVar_ID_93689 Human_SNP_ID_34265151 m1A Human chr1 + 153763281 153763281 153763281 TCGCTTCCACCCTATCAAGGAGACAGTTGTGGAGGAGCCAGTTGATATCACCCCTTACCTTGACC TCGCTTCCACCCTATCAAGGAGACAGTTGTGGCGGAGCCAGTTGATATCACCCCTTACCTTGACC A C INTS3 Ensembl:ENSG00000143624 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153763203..153763281 26863196 MeRIP-seq:(Medium) rs995293823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850406,Human_RBP_ID_3933994,Human_RBP_ID_5108749,Human_RBP_ID_9342991,Human_RBP_ID_9356839,Human_RBP_ID_18551867,Human_RBP_ID_18965977,Human_RBP_ID_26309809,Human_RBP_ID_27798534 Human_Splice_Rec_132140,Human_Splice_Rec_132141,Human_Splice_Rec_132200,Human_Splice_Rec_132201,Human_Splice_Rec_132256,Human_Splice_Rec_132257,Human_Splice_Rec_132302,Human_Splice_Rec_132303,Human_Splice_Rec_132348,Human_Splice_Rec_132349,Human_Splice_Rec_132392,Human_Splice_Rec_132393 Human_miRNA_ID_334341,Human_miRNA_ID_470074,Human_miRNA_ID_475899,Human_miRNA_ID_792786,Human_miRNA_ID_2068127,Human_miRNA_ID_2082188 RMVar_hsa_circ_113049,RMVar_hsa_circ_136268,RMVar_hsa_circ_24292,RMVar_hsa_circ_105743,RMVar_hsa_circ_120592,RMVar_hsa_circ_136279,RMVar_hsa_circ_96334,RMVar_hsa_circ_136278,RMVar_hsa_circ_116662,RMVar_hsa_circ_24624,RMVar_hsa_circ_136282,RMVar_hsa_circ_136283,RMVar_hsa_circ_115117,RMVar_hsa_circ_136287,RMVar_hsa_circ_361592,RMVar_hsa_circ_81847,RMVar_hsa_circ_136288,RMVar_hsa_circ_293536,RMVar_hsa_circ_306712,RMVar_hsa_circ_91267,RMVar_hsa_circ_136291,RMVar_hsa_circ_136293,RMVar_hsa_circ_51749,RMVar_hsa_circ_136292,RMVar_hsa_circ_136294,RMVar_hsa_circ_281911,RMVar_hsa_circ_136295,RMVar_hsa_circ_324021 93690 RMVar_ID_93690 Human_SNP_ID_34277903 m1A Human chr1 + 153809497 153809497 153809497 CTTTCCCCTCATTCTTAGAGCCCAACTTCAGTACCAAACACTGCCACCCAAATTGTCCAGCCCCC CTTTCCCCTCATTCTTAGAGCCCAACTTCAGTTCCAAACACTGCCACCCAAATTGTCCAGCCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153809448..153809522 26863196 MeRIP-seq:(Medium) rs553456953 Functional Loss SNV dbSNP153 33..33 33 - - - 93691 RMVar_ID_93691 Human_SNP_ID_34279685 m1A Human chr1 - 153816385 153816385 153816385 AAACAGCTGGAAAAGACACTCCTGGAGATCCCACCCCCTAAACCTCCTGCTCCCTTACTTCATTT AAACAGCTGGAAAAGACACTCCTGGAGATCCCGCCCCCTAAACCTCCTGCTCCCTTACTTCATTT T C GATAD2B Ensembl:ENSG00000143614 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153816251..153816525 26863196 MeRIP-seq:(Medium) rs768941302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9359350,Human_RBP_ID_10585227 RMVar_hsa_circ_28731,RMVar_hsa_circ_121103,RMVar_hsa_circ_269744,RMVar_hsa_circ_32482,RMVar_hsa_circ_111817,RMVar_hsa_circ_136304,RMVar_hsa_circ_136305,RMVar_hsa_circ_136306,RMVar_hsa_circ_93080,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971 93692 RMVar_ID_93692 Human_SNP_ID_34308530 m1A Human chr1 - 153922356 153922356 153922356 CACGCCCCGTTTCCCCCGCCATCCCCGCTTTCACTCCCTGCCTCATGCCCGCCATGCTCCCCTCC CACGCCCCGTTTCCCCCGCCATCCCCGCTTTCCCTCCCTGCCTCATGCCCGCCATGCTCCCCTCC T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153922348..153922519 26863196 MeRIP-seq:(Medium) rs1464129522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330407,Human_RBP_ID_5125292,Human_RBP_ID_17072464,Human_RBP_ID_18928605,Human_RBP_ID_24398840,Human_RBP_ID_26774531 93693 RMVar_ID_93693 Human_SNP_ID_34308536 m1A Human chr1 + 153922377 153922376 153922377 GAGGCAGGGAGTGAAAGCGGGGATGGCGGGGGAAACGGGGCGTGAGGGAGGGGAGAAAGAGTACA GAGGCAGGGAGTGAAAGCGGGGATGGCGGGGG_AACGGGGCGTGAGGGAGGGGAGAAAGAGTACA GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153922326..153922475 26863196 MeRIP-seq:(Medium) rs1190429205 Functional Loss DEL dbSNP153 33..33 33 - - - 93694 RMVar_ID_93694 Human_SNP_ID_34311576 m1A Human chr1 - 153932929 153932929 153932929 GGCTGGGCACCTGATGACTCTAACCTCAACACAACCTGCCCCTTCTGCGCCTGCCCCTTTGTGCC GGCTGGGCACCTGATGACTCTAACCTCAACACGACCTGCCCCTTCTGCGCCTGCCCCTTTGTGCC T C DENND4B Ensembl:ENSG00000198837 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153932880..153933014 26863196 MeRIP-seq:(Medium) rs1357635660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327027,Human_RBP_ID_17726227,Human_RBP_ID_18428573,Human_RBP_ID_22847202 Human_Splice_Rec_132733,Human_Splice_Rec_132753,Human_Splice_Rec_132761,Human_Splice_Rec_132763 Human_miRNA_ID_2383578 RMVar_hsa_circ_13679,RMVar_hsa_circ_128047,RMVar_hsa_circ_17629,RMVar_hsa_circ_136312,RMVar_hsa_circ_136316,RMVar_hsa_circ_104692,RMVar_hsa_circ_116711,RMVar_hsa_circ_94517,RMVar_hsa_circ_136317,RMVar_hsa_circ_106447,RMVar_hsa_circ_136318,RMVar_hsa_circ_136319 93695 RMVar_ID_93695 Human_SNP_ID_34311786 m1A Human chr1 - 153933555 153933555 153933555 ATTCCCCCACCTGAGCTGCCTCCTGACCTGCCACCCCCAGCCCGCCGCAGCCCCATGGACAGTCT ATTCCCCCACCTGAGCTGCCTCCTGACCTGCCCCCCCCAGCCCGCCGCAGCCCCATGGACAGTCT T G DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153933504..153933622 26863196 MeRIP-seq:(Medium) rs1017020435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744463,Human_RBP_ID_5458538,Human_RBP_ID_18928608 Human_Splice_Rec_132729,Human_Splice_Rec_132803 Human_miRNA_ID_2682866 RMVar_hsa_circ_128047,RMVar_hsa_circ_17629,RMVar_hsa_circ_136312,RMVar_hsa_circ_136316,RMVar_hsa_circ_104692,RMVar_hsa_circ_116711,RMVar_hsa_circ_94517,RMVar_hsa_circ_136317,RMVar_hsa_circ_106447,RMVar_hsa_circ_82827,RMVar_hsa_circ_136318,RMVar_hsa_circ_136319,RMVar_hsa_circ_80114,RMVar_hsa_circ_136320,RMVar_hsa_circ_136321 93696 RMVar_ID_93696 Human_SNP_ID_34312730 m1A Human chr1 + 153936651 153936651 153936651 AGGGTGCCGACCGCACATAGGCAGGCAGACACAGGAACCACAGCCCATAGCAGTGCCCCAGCAGG AGGGTGCCGACCGCACATAGGCAGGCAGACACGGGAACCACAGCCCATAGCAGTGCCCCAGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:153936602..153937542 32194978 MeRIP-seq:(Medium) rs754098427 Functional Loss SNV dbSNP153 33..33 33 - - - 93697 RMVar_ID_93697 Human_SNP_ID_34314559 m1A Human chr1 - 153943073 153943073 153943073 CCCAAGCCTGGCTTCCAAGTGCTTGACACGACACCCTACAGCCACTCAGCAAACCTGGCCCCTCC CCCAAGCCTGGCTTCCAAGTGCTTGACACGACGCCCTACAGCCACTCAGCAAACCTGGCCCCTCC T C DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153942951..153943154 26863196 MeRIP-seq:(Medium) rs754892693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18187270,Human_RBP_ID_18552001 Human_Splice_Rec_132694,Human_Splice_Rec_132768,Human_Splice_Rec_132818 RMVar_hsa_circ_28451,RMVar_hsa_circ_124737,RMVar_hsa_circ_136323,RMVar_hsa_circ_99777,RMVar_hsa_circ_136337 93698 RMVar_ID_93698 Human_SNP_ID_34314560 m1A Human chr1 - 153943073 153943073 153943073 CCCAAGCCTGGCTTCCAAGTGCTTGACACGACACCCTACAGCCACTCAGCAAACCTGGCCCCTCC CCCAAGCCTGGCTTCCAAGTGCTTGACACGACCCCCTACAGCCACTCAGCAAACCTGGCCCCTCC T G DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153942951..153943154 26863196 MeRIP-seq:(Medium) rs754892693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18187270,Human_RBP_ID_18552001 Human_Splice_Rec_132694,Human_Splice_Rec_132768,Human_Splice_Rec_132818 RMVar_hsa_circ_28451,RMVar_hsa_circ_124737,RMVar_hsa_circ_136323,RMVar_hsa_circ_99777,RMVar_hsa_circ_136337 93699 RMVar_ID_93699 Human_SNP_ID_34314842 m1A Human chr1 - 153944111 153944111 153944111 GAACTCAGTGCTGGACTTCTGGGTGGAACTCAACCCGTCATCTGCTACCGCAGGGGCCGTGACAA GAACTCAGTGCTGGACTTCTGGGTGGAACTCAGCCCGTCATCTGCTACCGCAGGGGCCGTGACAA T C DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:153944035..153944145 26863196 MeRIP-seq:(Medium) rs368659630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18968968,Human_RBP_ID_27798548 Human_Splice_Rec_132693,Human_Splice_Rec_132767,Human_Splice_Rec_132817 RMVar_hsa_circ_28451 93700 RMVar_ID_93700 Human_SNP_ID_34314881 m1A Human chr1 - 153944246 153944246 153944246 GAACCCAGTGGGCCCCTGCGCCCTCCCCGGCCAGCTGAGCCCATCACAGATGTGGCAGTCATCGC GAACCCAGTGGGCCCCTGCGCCCTCCCCGGCCGGCTGAGCCCATCACAGATGTGGCAGTCATCGC T C DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153944203..153944274 26863196 MeRIP-seq:(Medium) rs200382412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271848,Human_RBP_ID_4075968,Human_RBP_ID_22536285 Human_miRNA_ID_675514 RMVar_hsa_circ_28451 93701 RMVar_ID_93701 Human_SNP_ID_34315447 m1A Human chr1 - 153946543 153946514 153946543 GAGGACCGAGCCGGCCGAGCGAGCAGCGCGGCAGCACAGTCCCCGCGTGGCGCAGCGCGGCGGGG GAGGACCGAGCCGGCCGAGCGAGCAGCGCGGC_____________________________GGGG CGCCGCGCTGCGCCACGCGGGGACTGTGCT C DENND4B Ensembl:ENSG00000198837 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153946425..153946635 26863196 MeRIP-seq:(Medium) rs1350574385 Functional Loss DEL dbSNP153 33..61 33 - - - Human_RBP_ID_3328572,Human_RBP_ID_4073031,Human_RBP_ID_5311821,Human_RBP_ID_9411262,Human_RBP_ID_18415627,Human_RBP_ID_26311830,Human_RBP_ID_26773150 93702 RMVar_ID_93702 Human_SNP_ID_34315472 m1A Human chr1 - 153946623 153946623 153946623 CGGCCCGGAGCGGGGGTTGGGGGAGTAGAGAAAGCGGGGCGCGCGGAGGAACGCTGGGTCCCCGG CGGCCCGGAGCGGGGGTTGGGGGAGTAGAGAAGGCGGGGCGCGCGGAGGAACGCTGGGTCCCCGG T C DENND4B Ensembl:ENSG00000198837 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153946264..153946725 26863196 MeRIP-seq:(Medium) rs954972509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855269,Human_RBP_ID_3328572,Human_RBP_ID_3934042,Human_RBP_ID_4073031,Human_RBP_ID_5109900,Human_RBP_ID_5136371,Human_RBP_ID_5158501,Human_RBP_ID_5311821,Human_RBP_ID_5335871,Human_RBP_ID_9319157,Human_RBP_ID_9411262,Human_RBP_ID_17646538,Human_RBP_ID_18415064,Human_RBP_ID_18968969,Human_RBP_ID_26311830,Human_RBP_ID_26773150 93703 RMVar_ID_93703 Human_SNP_ID_34315500 m1A Human chr1 - 153946687 153946687 153946687 CAGACGCTTGCCAGGGTCACGGCCGCCGGCCGAGGAGGAGGGGTGGGGGTAGCGGCGGCGCCCGC CAGACGCTTGCCAGGGTCACGGCCGCCGGCCGTGGAGGAGGGGTGGGGGTAGCGGCGGCGCCCGC T A DENND4B Ensembl:ENSG00000198837 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:153946587..153946704 26863410 MeRIP-seq:(Medium) rs1227372103 Functional Loss SNV dbSNP153 33..33 33 - - - 93704 RMVar_ID_93704 Human_SNP_ID_34315501 m1A Human chr1 - 153946687 153946687 153946687 CAGACGCTTGCCAGGGTCACGGCCGCCGGCCGAGGAGGAGGGGTGGGGGTAGCGGCGGCGCCCGC CAGACGCTTGCCAGGGTCACGGCCGCCGGCCGGGGAGGAGGGGTGGGGGTAGCGGCGGCGCCCGC T C DENND4B Ensembl:ENSG00000198837 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:153946587..153946704 26863410 MeRIP-seq:(Medium) rs1227372103 Functional Loss SNV dbSNP153 33..33 33 - - - 93705 RMVar_ID_93705 Human_SNP_ID_34317006 m1A Human chr1 + 153951997 153951997 153951997 ATCCCTCCAGTCAGGCAGCACCCAGTGGGCACATGGCCAGGACAGTCACTCACCTGGTGCATCAT ATCCCTCCAGTCAGGCAGCACCCAGTGGGCACGTGGCCAGGACAGTCACTCACCTGGTGCATCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153951994..153952257 26863196 MeRIP-seq:(Medium) rs566679859 Functional Loss SNV dbSNP153 33..33 33 - - - 93706 RMVar_ID_93706 Human_SNP_ID_34317023 m1A Human chr1 - 153952034 153952034 153952034 CTGGGCATCAGCAGGGGCATGGGCCTGGGCCCAGGCTATGATGCACCAGGTGAGTGACTGTCCTG CTGGGCATCAGCAGGGGCATGGGCCTGGGCCCGGGCTATGATGCACCAGGTGAGTGACTGTCCTG T C CRTC2 Ensembl:ENSG00000160741 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153952001..153952050 26863196 MeRIP-seq:(Medium) rs1211182815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17223501,Human_RBP_ID_18552016 Human_Splice_Rec_132835,Human_Splice_Rec_132855,Human_Splice_Rec_132887,Human_Splice_Rec_132909 RMVar_hsa_circ_56096,RMVar_hsa_circ_83539,RMVar_hsa_circ_94064,RMVar_hsa_circ_136338,RMVar_hsa_circ_136339,RMVar_hsa_circ_53851,RMVar_hsa_circ_317828 93707 RMVar_ID_93707 Human_SNP_ID_34317442 m1A Human chr1 + 153953315 153953315 153953315 AGGATGCTGGGAGGTGTGGGGCCTGGGTAGGTATCCTGGGGACTGGGGTTCATCACACTTGTATG AGGATGCTGGGAGGTGTGGGGCCTGGGTAGGTGTCCTGGGGACTGGGGTTCATCACACTTGTATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153953238..153953328 26863196 MeRIP-seq:(Medium) rs1487350625 Functional Loss SNV dbSNP153 33..33 33 - - - 93708 RMVar_ID_93708 Human_SNP_ID_34317921 m1A Human chr1 - 153954975 153954975 153954975 TTCTGTCCTTTTTGGCAGAGCCCCCTCCACTCACCTTTGGATTCATCTCGGAGCACTCGGCACCA TTCTGTCCTTTTTGGCAGAGCCCCCTCCACTCGCCTTTGGATTCATCTCGGAGCACTCGGCACCA T C CRTC2 Ensembl:ENSG00000160741 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:153954925..153958067 32194978 MeRIP-seq:(Medium) rs774330877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22126,Human_RBP_ID_1149711,Human_RBP_ID_3995471,Human_RBP_ID_5331954,Human_RBP_ID_10587816,Human_RBP_ID_17726255,Human_RBP_ID_19043935,Human_RBP_ID_22535472,Human_RBP_ID_22634339 Human_Splice_Rec_132874,Human_Splice_Rec_132926,Human_Splice_Rec_132934 Human_miRNA_ID_2064251,Human_miRNA_ID_2702128,Human_miRNA_ID_2933432 RMVar_hsa_circ_40937,RMVar_hsa_circ_317828,RMVar_hsa_circ_104348,RMVar_hsa_circ_136340,RMVar_hsa_circ_292921,RMVar_hsa_circ_49440,RMVar_hsa_circ_296080 93709 RMVar_ID_93709 Human_SNP_ID_34318862 m1A Human chr1 + 153958530 153958530 153958530 CTTCCTTCCCCGTCCCTCCCTGCCACCCTCCCAGTACCAGCCGCGGCCTCCGCCGCGGCCTCGGC CTTCCTTCCCCGTCCCTCCCTGCCACCCTCCCTGTACCAGCCGCGGCCTCCGCCGCGGCCTCGGC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:153958446..153958572 26863410 MeRIP-seq:(Medium) rs1404864965 Functional Loss SNV dbSNP153 33..33 33 - - - 93710 RMVar_ID_93710 Human_SNP_ID_34319152 m1A Human chr1 - 153959577 153959577 153959577 AGGGGACTGGCGCCAAATGGTCTCTCCCTGCCAATTTTGGTATCTTCTCTGGCCTCTCCAGTCCT AGGGGACTGGCGCCAAATGGTCTCTCCCTGCCGATTTTGGTATCTTCTCTGGCCTCTCCAGTCCT T C SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:153959526..153959675 26863196 MeRIP-seq:(Medium) rs1360838445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327101,Human_RBP_ID_5109216,Human_RBP_ID_8168338,Human_RBP_ID_10587989,Human_RBP_ID_18217319,Human_RBP_ID_18928619,Human_RBP_ID_23333782,Human_RBP_ID_26368786 Human_miRNA_ID_137702,Human_miRNA_ID_414375 RMVar_hsa_circ_77644,RMVar_hsa_circ_136342 93711 RMVar_ID_93711 Human_SNP_ID_34319972 m1A Human chr1 + 153962570 153962570 153962570 CATGGTTAGCTCCTGGCCGGCGCAGCACACAGATGGGCACCAGGCTGCAGAGGAGGGTGAGCACC CATGGTTAGCTCCTGGCCGGCGCAGCACACAGGTGGGCACCAGGCTGCAGAGGAGGGTGAGCACC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:153962551..153962575 26863196 MeRIP-seq:(Medium) rs369281695 Functional Loss SNV dbSNP153 33..33 33 - - - 93712 RMVar_ID_93712 Human_SNP_ID_34319996 m1A Human chr1 - 153962633 153962633 153962633 AGCTTCAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGG AGCTTCAGAGCCTCCAGTGCCTGTGGGGCTGGGGGTGAAGTTGGGGGCCCTGGTGCTGCTGCTGG T C SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153962583..153962700 26863196 MeRIP-seq:(Medium) rs1407450707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224147,Human_RBP_ID_745092,Human_RBP_ID_4073035,Human_RBP_ID_9320179,Human_RBP_ID_22427528 93713 RMVar_ID_93713 Human_SNP_ID_34320208 m1A Human chr1 + 153963482 153963482 153963482 CTGGGCAGCCGACATGGACCCCGCTGCCAGACAGCCCGCACTCACCTCGCGAGGGTCTCACTACA CTGGGCAGCCGACATGGACCCCGCTGCCAGACGGCCCGCACTCACCTCGCGAGGGTCTCACTACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:153963476..153963575 26863196 MeRIP-seq:(Medium) rs1418352506 Functional Loss SNV dbSNP153 33..33 33 - - - 93714 RMVar_ID_93714 Human_SNP_ID_34321257 m1A Human chr1 - 153967551 153967551 153967551 GACCTCCCGGGCTCAGGTGATTCTCCCGCCTCAGCACCGCGAGCAGCTAGGACCACAGGCGCGAG GACCTCCCGGGCTCAGGTGATTCTCCCGCCTCTGCACCGCGAGCAGCTAGGACCACAGGCGCGAG T A SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:153967522..153967645 26863196 MeRIP-seq:(Medium) rs368076810 Functional Loss SNV dbSNP153 33..33 33 - - - 93715 RMVar_ID_93715 Human_SNP_ID_34321262 m1A Human chr1 - 153967582 153967581 153967582 GGTGGTGCGATCACGGTTCCATGCAGCCCCCGACCTCCCGGGCTCAGGTGATTCTCCCGCCTCAG GGTGGTGCGATCACGGTTCCATGCAGCCCCCG_CCTCCCGGGCTCAGGTGATTCTCCCGCCTCAG GT G SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153967532..153967683 26863196 MeRIP-seq:(Medium) rs1471201864 Functional Loss DEL dbSNP153 33..33 33 - - - 93716 RMVar_ID_93716 Human_SNP_ID_34321263 m1A Human chr1 - 153967582 153967582 153967582 GGTGGTGCGATCACGGTTCCATGCAGCCCCCGACCTCCCGGGCTCAGGTGATTCTCCCGCCTCAG GGTGGTGCGATCACGGTTCCATGCAGCCCCCGGCCTCCCGGGCTCAGGTGATTCTCCCGCCTCAG T C SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153967532..153967683 26863196 MeRIP-seq:(Medium) rs887009026 Functional Loss SNV dbSNP153 33..33 33 - - - 93717 RMVar_ID_93717 Human_SNP_ID_34321436 m1A Human chr1 + 153968289 153968289 153968289 TTGGGGAGGTCAACGGGCTATGCTGGCTTGACAGGGCTGGGCTCTTCAGAACAGGTAATGCTTGG TTGGGGAGGTCAACGGGCTATGCTGGCTTGACCGGGCTGGGCTCTTCAGAACAGGTAATGCTTGG A C CREB3L4 Ensembl:ENSG00000143578 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:153968239..153968354 26863196 MeRIP-seq:(Medium) rs1182967402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_133071,Human_Splice_Rec_133079,Human_Splice_Rec_133097,Human_Splice_Rec_133115,Human_Splice_Rec_133119,Human_Splice_Rec_133127,Human_Splice_Rec_133129 93718 RMVar_ID_93718 Human_SNP_ID_34324191 m1A Human chr1 + 153977299 153977299 153977299 CGCACCTGTCGGAACAGAGGGACCTACTCCACAGGCCTCGTGCCTCCGTCGGAGCGCAGAGGCGG CGCACCTGTCGGAACAGAGGGACCTACTCCACGGGCCTCGTGCCTCCGTCGGAGCGCAGAGGCGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:153977276..153977300 32194978 MeRIP-seq:(Medium) rs1557889632 Functional Loss SNV dbSNP153 33..33 33 - - - 93719 RMVar_ID_93719 Human_SNP_ID_34324243 m1A Human chr1 - 153977480 153977480 153977480 CGGCCCTTCCTCCAGCGCCCTGCGGACCCCGCAGAAGGCGCTCGCCTCCCTAGCCCGCAAAAACA CGGCCCTTCCTCCAGCGCCCTGCGGACCCCGCGGAAGGCGCTCGCCTCCCTAGCCCGCAAAAACA T C AL358472.6,JTB Ensembl:ENSG00000285641,Ensembl:ENSG00000143543 Protein coding,Protein coding 3'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:153977326..153977675 26863410 MeRIP-seq:(Medium) rs1235340579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327182,Human_RBP_ID_745086,Human_RBP_ID_3995659,Human_RBP_ID_17338434,Human_RBP_ID_22429693 93720 RMVar_ID_93720 Human_SNP_ID_34324244 m1A Human chr1 - 153977480 153977480 153977480 CGGCCCTTCCTCCAGCGCCCTGCGGACCCCGCAGAAGGCGCTCGCCTCCCTAGCCCGCAAAAACA CGGCCCTTCCTCCAGCGCCCTGCGGACCCCGCCGAAGGCGCTCGCCTCCCTAGCCCGCAAAAACA T G AL358472.6,JTB Ensembl:ENSG00000285641,Ensembl:ENSG00000143543 Protein coding,Protein coding 3'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:153977326..153977675 26863410 MeRIP-seq:(Medium) rs1235340579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327182,Human_RBP_ID_745086,Human_RBP_ID_3995659,Human_RBP_ID_17338434,Human_RBP_ID_22429693 93721 RMVar_ID_93721 Human_SNP_ID_34325356 m1A Human chr1 - 153981927 153981927 153981927 AAGGGAAAAGCAGAAAGGAAAAAAAGGAAGAGAGAGGAAGGGAGAAGGGAGAGGAATGAATTGAG AAGGGAAAAGCAGAAAGGAAAAAAAGGAAGAGGGAGGAAGGGAGAAGGGAGAGGAATGAATTGAG T C AL358472.6,RAB13 Ensembl:ENSG00000285641,Ensembl:ENSG00000143545 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:153981826..153982200 26863196 MeRIP-seq:(Medium) rs1435638164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258532 RMVar_hsa_circ_136344,RMVar_hsa_circ_124620,RMVar_hsa_circ_98861,RMVar_hsa_circ_136345 93722 RMVar_ID_93722 Human_SNP_ID_34325548 m1A Human chr1 - 153982410 153982410 153982410 TTTTAGTTCCCTGGCCCGGGACATCTTGCTCAAGTCAGGAGGCCGGAGATCAGTAAGTTGGTTTT TTTTAGTTCCCTGGCCCGGGACATCTTGCTCACGTCAGGAGGCCGGAGATCAGTAAGTTGGTTTT T G AL358472.6,RAB13 Ensembl:ENSG00000285641,Ensembl:ENSG00000143545 Protein coding,Protein coding CDS,CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1049574987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_133196,Human_Splice_Rec_133197,Human_Splice_Rec_133218,Human_Splice_Rec_133219,Human_Splice_Rec_133232,Human_Splice_Rec_133233,Human_Splice_Rec_133250,Human_Splice_Rec_133251 RMVar_hsa_circ_378,RMVar_hsa_circ_136344,RMVar_hsa_circ_124620,RMVar_hsa_circ_98861,RMVar_hsa_circ_136345 93723 RMVar_ID_93723 Human_SNP_ID_34325788 m1A Human chr1 - 153983171 153983171 153983171 AAGAGATGGGGAAACTGGTTAGAACCTGGAGAATGAAGGGGTCCATCAGGATAGGCAAGACCTAA AAGAGATGGGGAAACTGGTTAGAACCTGGAGAGTGAAGGGGTCCATCAGGATAGGCAAGACCTAA T C AL358472.6,RAB13 Ensembl:ENSG00000285641,Ensembl:ENSG00000143545 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153983168..153983239 26863196 MeRIP-seq:(Medium) rs1316643465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23333874 RMVar_hsa_circ_136344,RMVar_hsa_circ_124620,RMVar_hsa_circ_98861,RMVar_hsa_circ_136345 93724 RMVar_ID_93724 Human_SNP_ID_34325907 m1A Human chr1 - 153983577 153983577 153983577 CATCCCATGAAAACTTCTCCTTCTTTAGGGACACGGCTGGCCAAGAGCGGTTCAAGACAATAACT CATCCCATGAAAACTTCTCCTTCTTTAGGGACGCGGCTGGCCAAGAGCGGTTCAAGACAATAACT T C AL358472.6,RAB13 Ensembl:ENSG00000285641,Ensembl:ENSG00000143545 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153983526..153983600 26863196 MeRIP-seq:(Medium) rs977469670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858986 Human_Splice_Rec_133188,Human_Splice_Rec_133189,Human_Splice_Rec_133210,Human_Splice_Rec_133211,Human_Splice_Rec_133224,Human_Splice_Rec_133225,Human_Splice_Rec_133238,Human_Splice_Rec_133242,Human_Splice_Rec_133243,Human_Splice_Rec_133256,Human_Splice_Rec_133257 RMVar_hsa_circ_136344,RMVar_hsa_circ_124620,RMVar_hsa_circ_98861,RMVar_hsa_circ_136345 93725 RMVar_ID_93725 Human_SNP_ID_34326459 m1A Human chr1 + 153986045 153986045 153986045 TTACTCTAAGGGGACTGAAAAGTGGGGTCACTAGTAATCCGGGAGCCGGAGAAGGAGGTCACAGG TTACTCTAAGGGGACTGAAAAGTGGGGTCACTGGTAATCCGGGAGCCGGAGAAGGAGGTCACAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153985363..153986112 26863196 MeRIP-seq:(Medium) rs1231497573 Functional Loss SNV dbSNP153 33..33 33 - - - 93726 RMVar_ID_93726 Human_SNP_ID_34328015 m1A Human chr1 + 153990794 153990794 153990794 CCTTTCCGGCGGTGACGACCTACGCACACGAGAACATGCCTGTGAGTGCTTTGGTCCAGGTTTCG CCTTTCCGGCGGTGACGACCTACGCACACGAGGACATGCCTGTGAGTGCTTTGGTCCAGGTTTCG A G RPS27 Ensembl:ENSG00000177954 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153990758..153990858 26863196 MeRIP-seq:(Medium) rs766410015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222950,Human_RBP_ID_744209,Human_RBP_ID_802285,Human_RBP_ID_1412308,Human_RBP_ID_4074435,Human_RBP_ID_10588171,Human_RBP_ID_17338436,Human_RBP_ID_17456307,Human_RBP_ID_22026047,Human_RBP_ID_22531978,Human_RBP_ID_23333875,Human_RBP_ID_26801029 Human_Splice_Rec_133261,Human_Splice_Rec_133263,Human_Splice_Rec_133275 RMVar_hsa_circ_136347,RMVar_hsa_circ_82786,RMVar_hsa_circ_107976,RMVar_hsa_circ_136348 93727 RMVar_ID_93727 Human_SNP_ID_34328024 m1A Human chr1 - 153990802 153990802 153990802 ATCTCCGCCGAAACCTGGACCAAAGCACTCACAGGCATGTTCTCGTGTGCGTAGGTCGTCACCGC ATCTCCGCCGAAACCTGGACCAAAGCACTCACTGGCATGTTCTCGTGTGCGTAGGTCGTCACCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HeLa cell line,mRNA;HEK293T,Wild Type chr1:153990751..153991025;chr1:153990751..153990850 26863196,26863410 MeRIP-seq:(Medium) rs1448259293 Functional Loss SNV dbSNP153 33..33 33 - - - 93728 RMVar_ID_93728 Human_SNP_ID_34368338 m1A Human chr1 - 154156965 154156965 154156965 TTTTCATTAGAAGTTACCAAATTAAGATGGTAAGACCTCTGAGACCAAAATTTTGTCCCATCTCT TTTTCATTAGAAGTTACCAAATTAAGATGGTAGGACCTCTGAGACCAAAATTTTGTCCCATCTCT T C TPM3 Ensembl:ENSG00000143549 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154156914..154156986 26863196 MeRIP-seq:(Medium) rs1280417684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327243,Human_RBP_ID_2094930,Human_RBP_ID_3995714,Human_RBP_ID_5692650,Human_RBP_ID_8168345,Human_RBP_ID_10589200,Human_RBP_ID_19195079,Human_RBP_ID_22128170,Human_RBP_ID_22780187,Human_RBP_ID_23333960,Human_RBP_ID_24395470,Human_RBP_ID_24455217,Human_RBP_ID_26389824,Human_RBP_ID_26842347,Human_RBP_ID_27168568 93729 RMVar_ID_93729 Human_SNP_ID_34368380 m1A Human chr1 - 154157174 154157170 154157174 GAAAAGGTGTAGGCCTGCCTTACCGAGAGCCAAACAGAGCCCAGGGAGACTCCGCTGTGGGAAAC GAAAAGGTGTAGGCCTGCCTTACCGAGAGCCA____GAGCCCAGGGAGACTCCGCTGTGGGAAAC CTGTT C TPM3 Ensembl:ENSG00000143549 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154157101..154157400 32194978 MeRIP-seq:(Medium) rs1405460933 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_224143,Human_RBP_ID_327247,Human_RBP_ID_5692657,Human_RBP_ID_8168347,Human_RBP_ID_10589206,Human_RBP_ID_17224006,Human_RBP_ID_17446346,Human_RBP_ID_17762894,Human_RBP_ID_18217353,Human_RBP_ID_26368859 93730 RMVar_ID_93730 Human_SNP_ID_34371629 m1A Human chr1 - 154170467 154170467 154170467 TGGTTCTGACTAATTTCATATTTCCCCCAGGCAGAGACCCGTGCTGAGTTTGCTGAGAGATCGGT TGGTTCTGACTAATTTCATATTTCCCCCAGGCGGAGACCCGTGCTGAGTTTGCTGAGAGATCGGT T C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154170401..154170475 32194978 MeRIP-seq:(Medium) rs373670110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222251,Human_RBP_ID_1064554,Human_RBP_ID_3995735,Human_RBP_ID_9356872,Human_RBP_ID_22634345,Human_RBP_ID_22735160,Human_RBP_ID_26311839,Human_RBP_ID_27800819 Human_Splice_Rec_133478,Human_Splice_Rec_133479,Human_Splice_Rec_133492,Human_Splice_Rec_133493,Human_Splice_Rec_133498,Human_Splice_Rec_133499,Human_Splice_Rec_133506,Human_Splice_Rec_133507,Human_Splice_Rec_133520,Human_Splice_Rec_133521,Human_Splice_Rec_133534,Human_Splice_Rec_133535,Human_Splice_Rec_133548,Human_Splice_Rec_133549,Human_Splice_Rec_133560,Human_Splice_Rec_133561,Human_Splice_Rec_133566,Human_Splice_Rec_133567,Human_Splice_Rec_133584,Human_Splice_Rec_133585,Human_Splice_Rec_133598,Human_Splice_Rec_133599,Human_Splice_Rec_133612,Human_Splice_Rec_133613,Human_Splice_Rec_133628,Human_Splice_Rec_133629,Human_Splice_Rec_133634,Human_Splice_Rec_133635,Human_Splice_Rec_133648,Human_Splice_Rec_133649,Human_Splice_Rec_133662,Human_Splice_Rec_133663,Human_Splice_Rec_133676,Human_Splice_Rec_133677,Human_Splice_Rec_133692,Human_Splice_Rec_133693,Human_Splice_Rec_133710,Human_Splice_Rec_133711,Human_Splice_Rec_133716,Human_Splice_Rec_133724 RMVar_hsa_circ_136356,RMVar_hsa_circ_285478,RMVar_hsa_circ_369627,RMVar_hsa_circ_279851,RMVar_hsa_circ_320725 93731 RMVar_ID_93731 Human_SNP_ID_34373300 m1A Human chr1 + 154176165 154176165 154176165 GCTTTTTCAGCTTCTTCCAGCTTTTGCAGGGCAGTGGCCAGGCGCTCCTGAGCACGGTCCAGCTC GCTTTTTCAGCTTCTTCCAGCTTTTGCAGGGCCGTGGCCAGGCGCTCCTGAGCACGGTCCAGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154176059..154176280 26863196 MeRIP-seq:(Medium) rs764255899 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_530 93732 RMVar_ID_93732 Human_SNP_ID_34374883 m1A Human chr1 - 154182991 154182991 154182991 CGAGAAGTTGAGGGAGAAAGGCGGGCCCGGGAACAGGTACGGAGATGGTGAGGCTCATGAGGGAG CGAGAAGTTGAGGGAGAAAGGCGGGCCCGGGAGCAGGTACGGAGATGGTGAGGCTCATGAGGGAG T C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1362613279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_190493,Human_RBP_ID_743267,Human_RBP_ID_802345,Human_RBP_ID_857343,Human_RBP_ID_4081861,Human_RBP_ID_5338438,Human_RBP_ID_9356883,Human_RBP_ID_22560271,Human_RBP_ID_23112579,Human_RBP_ID_24541221,Human_RBP_ID_24556226,Human_RBP_ID_26309812,Human_RBP_ID_27798561 Human_Splice_Rec_133469,Human_Splice_Rec_133481,Human_Splice_Rec_133501,Human_Splice_Rec_133509,Human_Splice_Rec_133523,Human_Splice_Rec_133551,Human_Splice_Rec_133573,Human_Splice_Rec_133589,Human_Splice_Rec_133601,Human_Splice_Rec_133651,Human_Splice_Rec_133665,Human_Splice_Rec_133717,Human_Splice_Rec_133753 RMVar_hsa_circ_85814,RMVar_hsa_circ_136357 93733 RMVar_ID_93733 Human_SNP_ID_34374890 m1A Human chr1 - 154183005 154183005 154183005 CTGAGCGCCTCCAGCGAGAAGTTGAGGGAGAAAGGCGGGCCCGGGAACAGGTACGGAGATGGTGA CTGAGCGCCTCCAGCGAGAAGTTGAGGGAGAAGGGCGGGCCCGGGAACAGGTACGGAGATGGTGA T C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:154182976..154183075 32194978 MeRIP-seq:(Medium) rs200139477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743267,Human_RBP_ID_802345,Human_RBP_ID_857343,Human_RBP_ID_9356884,Human_RBP_ID_22560271,Human_RBP_ID_24541222,Human_RBP_ID_24556226,Human_RBP_ID_26309812,Human_RBP_ID_27798561 Human_Splice_Rec_133469,Human_Splice_Rec_133481,Human_Splice_Rec_133501,Human_Splice_Rec_133509,Human_Splice_Rec_133523,Human_Splice_Rec_133551,Human_Splice_Rec_133573,Human_Splice_Rec_133589,Human_Splice_Rec_133601,Human_Splice_Rec_133651,Human_Splice_Rec_133665,Human_Splice_Rec_133717,Human_Splice_Rec_133753 RMVar_hsa_circ_85814,RMVar_hsa_circ_136357 93734 RMVar_ID_93734 Human_SNP_ID_34374918 m1A Human chr1 - 154183101 154183101 154183101 GCTGGGTGGGCACCATGGCTGGGATCACCACCATCGAGGCGGTGAAGCGCAAGATCCAGGTTCTG GCTGGGTGGGCACCATGGCTGGGATCACCACCTTCGAGGCGGTGAAGCGCAAGATCCAGGTTCTG T A TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:154183001..154183200 26863196 MeRIP-seq:(Medium) rs1165885225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101583,Human_RBP_ID_9356885,Human_RBP_ID_27798563 RMVar_hsa_circ_85814,RMVar_hsa_circ_136357 93735 RMVar_ID_93735 Human_SNP_ID_34374941 m1A Human chr1 - 154183140 154183140 154183140 CGCCGAGCGGAGGAGGCAGGAACCGGAGCGCGAGCAGTAGCTGGGTGGGCACCATGGCTGGGATC CGCCGAGCGGAGGAGGCAGGAACCGGAGCGCGCGCAGTAGCTGGGTGGGCACCATGGCTGGGATC T G TPM3 Ensembl:ENSG00000143549 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:154182976..154183225 26863196 MeRIP-seq:(Medium) rs763996113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101583,Human_RBP_ID_222257,Human_RBP_ID_860583,Human_RBP_ID_4081863,Human_RBP_ID_5312677,Human_RBP_ID_9356886,Human_RBP_ID_22871844,Human_RBP_ID_24556227,Human_RBP_ID_26311857,Human_RBP_ID_27798563 RMVar_hsa_circ_85814,RMVar_hsa_circ_136357 93736 RMVar_ID_93736 Human_SNP_ID_34374956 m1A Human chr1 - 154183151 154183151 154183151 GGAGGCTGCAACGCCGAGCGGAGGAGGCAGGAACCGGAGCGCGAGCAGTAGCTGGGTGGGCACCA GGAGGCTGCAACGCCGAGCGGAGGAGGCAGGATCCGGAGCGCGAGCAGTAGCTGGGTGGGCACCA T A TPM3 Ensembl:ENSG00000143549 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:154182976..154183200 26863196 MeRIP-seq:(Medium) rs11540112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101583,Human_RBP_ID_222257,Human_RBP_ID_743268,Human_RBP_ID_802346,Human_RBP_ID_860583,Human_RBP_ID_5312677,Human_RBP_ID_9356886,Human_RBP_ID_22871844,Human_RBP_ID_24556227,Human_RBP_ID_26311857,Human_RBP_ID_27798563 Human_miRNA_ID_3002454 RMVar_hsa_circ_85814,RMVar_hsa_circ_136357 93737 RMVar_ID_93737 Human_SNP_ID_34380915 m1A Human chr1 + 154206963 154206963 154206963 AGTGGAGCACAAAGGTAAGTTATTCCACATTCACCAACTTCCCCACTTGACCTCCCACCAGTTCC AGTGGAGCACAAAGGTAAGTTATTCCACATTCTCCAACTTCCCCACTTGACCTCCCACCAGTTCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154206913..154207080 26863196 MeRIP-seq:(Medium) rs1380530268 Functional Loss SNV dbSNP153 33..33 33 - - - 93738 RMVar_ID_93738 Human_SNP_ID_34381066 m1A Human chr1 - 154207563 154207563 154207563 ACCTAACTCAGTCCCCTGAGGTCTCCCCAACAACCATCCAGGTGACATACCTCCCCTCCAGTCAG ACCTAACTCAGTCCCCTGAGGTCTCCCCAACAGCCATCCAGGTGACATACCTCCCCTCCAGTCAG T C C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154207384..154207647 26863196 MeRIP-seq:(Medium) rs756416070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327294,Human_RBP_ID_1726034,Human_RBP_ID_8956340,Human_RBP_ID_17212615,Human_RBP_ID_17330465,Human_RBP_ID_17456549,Human_RBP_ID_17726378,Human_RBP_ID_18187273,Human_RBP_ID_26801039 Human_Splice_Rec_133788,Human_Splice_Rec_133800,Human_Splice_Rec_133814,Human_Splice_Rec_133822,Human_Splice_Rec_133832,Human_Splice_Rec_133842,Human_Splice_Rec_133852,Human_Splice_Rec_133854,Human_Splice_Rec_133858 Human_miRNA_ID_119,Human_miRNA_ID_3774,Human_miRNA_ID_7461,Human_miRNA_ID_11013,Human_miRNA_ID_18202,Human_miRNA_ID_21833,Human_miRNA_ID_25475,Human_miRNA_ID_1956129 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 93739 RMVar_ID_93739 Human_SNP_ID_34382480 m1A Human chr1 - 154212368 154212368 154212368 CTCTTCCTTTCTCTTTCCTAAGGTCTTTGGCCAGAATGAGTACCTACGCTATCAGGAGGCCCTGA CTCTTCCTTTCTCTTTCCTAAGGTCTTTGGCCGGAATGAGTACCTACGCTATCAGGAGGCCCTGA T C C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154212301..154212400 32194978 MeRIP-seq:(Medium) rs1250434723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855280,Human_RBP_ID_5333708,Human_RBP_ID_8956342,Human_RBP_ID_19039236,Human_RBP_ID_22427530,Human_RBP_ID_26386446,Human_RBP_ID_26798923 Human_Splice_Rec_133786,Human_Splice_Rec_133787,Human_Splice_Rec_133798,Human_Splice_Rec_133799,Human_Splice_Rec_133812,Human_Splice_Rec_133813,Human_Splice_Rec_133820,Human_Splice_Rec_133821,Human_Splice_Rec_133830,Human_Splice_Rec_133831,Human_Splice_Rec_133850,Human_Splice_Rec_133851,Human_Splice_Rec_133856,Human_Splice_Rec_133857,Human_Splice_Rec_133868,Human_Splice_Rec_133876 RMVar_hsa_circ_136362,RMVar_hsa_circ_136359,RMVar_hsa_circ_121933,RMVar_hsa_circ_270644,RMVar_hsa_circ_314962,RMVar_hsa_circ_274629,RMVar_hsa_circ_136363,RMVar_hsa_circ_136361 93740 RMVar_ID_93740 Human_SNP_ID_34382538 m1A Human chr1 - 154212478 154212478 154212478 CACTCATTGATACCCTTTTGGATGGCTATGAAACAGCCCGCTATGGGACAGGGGTAAGCCAGTTT CACTCATTGATACCCTTTTGGATGGCTATGAAGCAGCCCGCTATGGGACAGGGGTAAGCCAGTTT T C C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1215766960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327305,Human_RBP_ID_1412364,Human_RBP_ID_1726038,Human_RBP_ID_17338444,Human_RBP_ID_18552103,Human_RBP_ID_18966005,Human_RBP_ID_19039237,Human_RBP_ID_22128182,Human_RBP_ID_23334076,Human_RBP_ID_26798925 Human_Splice_Rec_133785,Human_Splice_Rec_133797,Human_Splice_Rec_133811,Human_Splice_Rec_133819,Human_Splice_Rec_133829,Human_Splice_Rec_133841,Human_Splice_Rec_133849,Human_Splice_Rec_133855,Human_Splice_Rec_133867,Human_Splice_Rec_133875 Human_miRNA_ID_2443350 RMVar_hsa_circ_136362,RMVar_hsa_circ_136359,RMVar_hsa_circ_121933,RMVar_hsa_circ_270644,RMVar_hsa_circ_314962,RMVar_hsa_circ_274629,RMVar_hsa_circ_136363,RMVar_hsa_circ_87644,RMVar_hsa_circ_136361,RMVar_hsa_circ_136364,RMVar_hsa_circ_60729 93741 RMVar_ID_93741 Human_SNP_ID_34383121 m1A Human chr1 - 154214513 154214513 154214513 CTCCAGGGTTCAGGATATCAAGTATGAGCCCCAGCTCCTTGCAGATGATGATGCTAGACTACTAC CTCCAGGGTTCAGGATATCAAGTATGAGCCCCGGCTCCTTGCAGATGATGATGCTAGACTACTAC T C C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154214418..154214536 26863196 MeRIP-seq:(Medium) rs1303684086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327317,Human_RBP_ID_971452,Human_RBP_ID_1412374,Human_RBP_ID_1726044,Human_RBP_ID_3282057,Human_RBP_ID_5692905,Human_RBP_ID_8286028,Human_RBP_ID_10590036,Human_RBP_ID_17212622,Human_RBP_ID_22780210,Human_RBP_ID_23334083,Human_RBP_ID_27579185 Human_Splice_Rec_133780,Human_Splice_Rec_133781,Human_Splice_Rec_133792,Human_Splice_Rec_133793,Human_Splice_Rec_133804,Human_Splice_Rec_133805,Human_Splice_Rec_133816,Human_Splice_Rec_133817,Human_Splice_Rec_133824,Human_Splice_Rec_133825,Human_Splice_Rec_133836,Human_Splice_Rec_133837,Human_Splice_Rec_133846,Human_Splice_Rec_133847,Human_Splice_Rec_133862,Human_Splice_Rec_133863,Human_Splice_Rec_133870,Human_Splice_Rec_133871 Human_miRNA_ID_2290914,Human_miRNA_ID_2356260,Human_miRNA_ID_2682870,Human_miRNA_ID_3058704 RMVar_hsa_circ_32958,RMVar_hsa_circ_136359,RMVar_hsa_circ_121933,RMVar_hsa_circ_314962,RMVar_hsa_circ_136363,RMVar_hsa_circ_60729,RMVar_hsa_circ_348330 93742 RMVar_ID_93742 Human_SNP_ID_34385002 m1A Human chr1 + 154220534 154220534 154220534 GGAGCTCCCCGGCCATTTCCTTACGGGGGAAGACCAAGCCAGACCCGGCCTGAAAACATGGCGGA GGAGCTCCCCGGCCATTTCCTTACGGGGGAAGCCCAAGCCAGACCCGGCCTGAAAACATGGCGGA A C UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154220302..154220625 26863196 MeRIP-seq:(Medium) rs563231443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121210,RMVar_hsa_circ_136366 93743 RMVar_ID_93743 Human_SNP_ID_34385003 m1A Human chr1 + 154220534 154220534 154220534 GGAGCTCCCCGGCCATTTCCTTACGGGGGAAGACCAAGCCAGACCCGGCCTGAAAACATGGCGGA GGAGCTCCCCGGCCATTTCCTTACGGGGGAAGGCCAAGCCAGACCCGGCCTGAAAACATGGCGGA A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154220302..154220625 26863196 MeRIP-seq:(Medium) rs563231443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121210,RMVar_hsa_circ_136366 93744 RMVar_ID_93744 Human_SNP_ID_34385008 m1A Human chr1 - 154220552 154220552 154220552 TCCCAGCTCTCCTGCCTGTCCGCCATGTTTTCAGGCCGGGTCTGGCTTGGTCTTCCCCCGTAAGG TCCCAGCTCTCCTGCCTGTCCGCCATGTTTTCTGGCCGGGTCTGGCTTGGTCTTCCCCCGTAAGG T A C1orf43 Ensembl:ENSG00000143612 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1373129862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222284,Human_RBP_ID_271858,Human_RBP_ID_327330,Human_RBP_ID_3995827,Human_RBP_ID_5234019,Human_RBP_ID_5692940,Human_RBP_ID_8735202,Human_RBP_ID_9320181,Human_RBP_ID_22128194,Human_RBP_ID_23334103 Human_miRNA_ID_3114852 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 93745 RMVar_ID_93745 Human_SNP_ID_34385018 m1A Human chr1 + 154220575 154220575 154220575 GACCCGGCCTGAAAACATGGCGGACAGGCAGGAGAGCTGGGAAAGGAGAACGACGCCTTCCAGCT GACCCGGCCTGAAAACATGGCGGACAGGCAGGCGAGCTGGGAAAGGAGAACGACGCCTTCCAGCT A C UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:154220526..154220575 26863196 MeRIP-seq:(Medium) rs1036921018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121210,RMVar_hsa_circ_136366 93746 RMVar_ID_93746 Human_SNP_ID_34385229 m1A Human chr1 - 154221042 154221042 154221042 GGGATCGCGGATTTAAAGGGGCCGCGGACAATACCCGGCCCCGCCGCGCTGCCGCTGCCGCCGCC GGGATCGCGGATTTAAAGGGGCCGCGGACAATCCCCGGCCCCGCCGCGCTGCCGCTGCCGCCGCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:154220951..154221070;chr1:154220951..154221095 26863410 MeRIP-seq:(Medium) rs899946886 Functional Loss SNV dbSNP153 33..33 33 - - - 93747 RMVar_ID_93747 Human_SNP_ID_34388689 m1A Human chr1 + 154234661 154234661 154234661 AGGCCAGAAGGATGGTGGCCAGACGGAATCCAATGAGGAAGGCAAAGAAAATCGAGACCGGGACA AGGCCAGAAGGATGGTGGCCAGACGGAATCCAGTGAGGAAGGCAAAGAAAATCGAGACCGGGACA A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:154227319..154234725;chr1:154228673..154235240 32194978 MeRIP-seq:(Medium) rs374548186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21227,Human_RBP_ID_3936673,Human_RBP_ID_8286067,Human_RBP_ID_8754124,Human_RBP_ID_9356888,Human_RBP_ID_10590935,Human_RBP_ID_17764096,Human_RBP_ID_24590943 Human_Splice_Rec_133884,Human_Splice_Rec_133885,Human_Splice_Rec_133930,Human_Splice_Rec_133931,Human_Splice_Rec_133976,Human_Splice_Rec_134026,Human_Splice_Rec_134027,Human_Splice_Rec_134036,Human_Splice_Rec_134037,Human_Splice_Rec_134054,Human_Splice_Rec_134072,Human_Splice_Rec_134073,Human_Splice_Rec_134122,Human_Splice_Rec_134123,Human_Splice_Rec_134140,Human_Splice_Rec_134141,Human_Splice_Rec_134152,Human_Splice_Rec_134153 Human_miRNA_ID_2997179,Human_miRNA_ID_2997180 RMVar_hsa_circ_106772,RMVar_hsa_circ_282860,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,RMVar_hsa_circ_350611,RMVar_hsa_circ_359817,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_317384,RMVar_hsa_circ_310695,RMVar_hsa_circ_36383,RMVar_hsa_circ_58333,RMVar_hsa_circ_72328,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_136370,RMVar_hsa_circ_136371,RMVar_hsa_circ_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_335129,RMVar_hsa_circ_287167,RMVar_hsa_circ_123093,RMVar_hsa_circ_33724,RMVar_hsa_circ_299716,RMVar_hsa_circ_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375,RMVar_hsa_circ_348380,RMVar_hsa_circ_365992,RMVar_hsa_circ_340534,RMVar_hsa_circ_57790,RMVar_hsa_circ_290058,RMVar_hsa_circ_46680,RMVar_hsa_circ_136376,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_136377 93748 RMVar_ID_93748 Human_SNP_ID_34388701 m1A Human chr1 - 154234701 154234701 154234701 CCCCGTCTTGGTGGCCCACCACGTCGCCGACTATAGTCTCTGTCCCGGTCTCGATTTTCTTTGCC CCCCGTCTTGGTGGCCCACCACGTCGCCGACTGTAGTCTCTGTCCCGGTCTCGATTTTCTTTGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:154234651..154234800 26863196 MeRIP-seq:(Medium) rs1558138671 Functional Loss SNV dbSNP153 33..33 33 - - - 93749 RMVar_ID_93749 Human_SNP_ID_34388705 m1A Human chr1 + 154234710 154234710 154234710 AATCGAGACCGGGACAGAGACTATAGTCGGCGACGTGGTGGGCCACCAAGACGGGGGAGAGGTGC AATCGAGACCGGGACAGAGACTATAGTCGGCGCCGTGGTGGGCCACCAAGACGGGGGAGAGGTGC A C UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154234560..154234813 26863196 MeRIP-seq:(Medium) rs985042195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21227,Human_RBP_ID_802453,Human_RBP_ID_2095083,Human_RBP_ID_3936674,Human_RBP_ID_5693140,Human_RBP_ID_8735209,Human_RBP_ID_9356888,Human_RBP_ID_10590935,Human_RBP_ID_17726408,Human_RBP_ID_24358905,Human_RBP_ID_24528788 Human_Splice_Rec_133885,Human_Splice_Rec_133931,Human_Splice_Rec_133977,Human_Splice_Rec_134027,Human_Splice_Rec_134037,Human_Splice_Rec_134055,Human_Splice_Rec_134073,Human_Splice_Rec_134123,Human_Splice_Rec_134141,Human_Splice_Rec_134153 RMVar_hsa_circ_106772,RMVar_hsa_circ_282860,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,RMVar_hsa_circ_350611,RMVar_hsa_circ_359817,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_317384,RMVar_hsa_circ_310695,RMVar_hsa_circ_36383,RMVar_hsa_circ_58333,RMVar_hsa_circ_72328,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_136370,RMVar_hsa_circ_136371,RMVar_hsa_circ_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_335129,RMVar_hsa_circ_287167,RMVar_hsa_circ_123093,RMVar_hsa_circ_33724,RMVar_hsa_circ_299716,RMVar_hsa_circ_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375,RMVar_hsa_circ_348380,RMVar_hsa_circ_365992,RMVar_hsa_circ_340534,RMVar_hsa_circ_57790,RMVar_hsa_circ_290058,RMVar_hsa_circ_46680,RMVar_hsa_circ_136376,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_136377 93750 RMVar_ID_93750 Human_SNP_ID_34388824 m1A Human chr1 - 154235152 154235151 154235153 ATAAAAATTAAAACAACAACAACAACAAAAAAACCAAACCACAGATGGCCAGAGCACAGTCAACA ATAAAAATTAAAACAACAACAACAACAAAAA__CCAAACCACAGATGGCCAGAGCACAGTCAACA GTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154235149..154235338 26863196 MeRIP-seq:(Medium) rs201031131 Functional Loss DEL dbSNP153 32..33 33 - - - 93751 RMVar_ID_93751 Human_SNP_ID_34388829 m1A Human chr1 - 154235152 154235152 154235152 ATAAAAATTAAAACAACAACAACAACAAAAAAACCAAACCACAGATGGCCAGAGCACAGTCAACA ATAAAAATTAAAACAACAACAACAACAAAAAACCCAAACCACAGATGGCCAGAGCACAGTCAACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154235149..154235338 26863196 MeRIP-seq:(Medium) rs942237274 Functional Loss SNV dbSNP153 33..33 33 - - - 93752 RMVar_ID_93752 Human_SNP_ID_34388873 m1A Human chr1 - 154235242 154235242 154235242 CCCCTTCTGCCTCTTTCTGTTCCTCTTCCAGAAGGCCCTCCACTCTTGGTGCCATCCAATCCATT CCCCTTCTGCCTCTTTCTGTTCCTCTTCCAGAGGGCCCTCCACTCTTGGTGCCATCCAATCCATT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:154235112..154235300 26863196 MeRIP-seq:(Medium) rs1338616421 Functional Loss SNV dbSNP153 33..33 33 - - - 93753 RMVar_ID_93753 Human_SNP_ID_34388874 m1A Human chr1 - 154235245 154235245 154235245 CGGCCCCTTCTGCCTCTTTCTGTTCCTCTTCCAGAAGGCCCTCCACTCTTGGTGCCATCCAATCC CGGCCCCTTCTGCCTCTTTCTGTTCCTCTTCCGGAAGGCCCTCCACTCTTGGTGCCATCCAATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154235176..154235300 26863196 MeRIP-seq:(Medium) rs1210155957 Functional Loss SNV dbSNP153 33..33 33 - - - 93754 RMVar_ID_93754 Human_SNP_ID_34389225 m1A Human chr1 - 154236554 154236553 154236554 CTCCTCGCCTACCAGAGCCACCTAAAGAAAGAATGAGAAAAAGAGAAGAGAGATGTATTTTAGAA CTCCTCGCCTACCAGAGCCACCTAAAGAAAGA_TGAGAAAAAGAGAAGAGAGATGTATTTTAGAA AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154236551..154236600 26863196 MeRIP-seq:(Medium) rs768531533 Functional Loss DEL dbSNP153 33..33 33 - - - 93755 RMVar_ID_93755 Human_SNP_ID_34392430 m1A Human chr1 + 154249334 154249334 154249334 TCCCAGTTCTTGGAGCAATTCAAGACTGCCCAAGCCCTGGCTCAGTTGGCAGCTCAGCATTCTCA TCCCAGTTCTTGGAGCAATTCAAGACTGCCCAGGCCCTGGCTCAGTTGGCAGCTCAGCATTCTCA A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154246209..154253925 32194978 MeRIP-seq:(Medium) rs755075789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21241,Human_RBP_ID_1726122,Human_RBP_ID_8735224,Human_RBP_ID_10591490,Human_RBP_ID_17212626,Human_RBP_ID_26842453 Human_Splice_Rec_133896,Human_Splice_Rec_133942,Human_Splice_Rec_133988,Human_Splice_Rec_134084,Human_Splice_Rec_134164,Human_Splice_Rec_134196 RMVar_hsa_circ_6037,RMVar_hsa_circ_106772,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_350611,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_36383,RMVar_hsa_circ_58333,RMVar_hsa_circ_72328,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_268210,RMVar_hsa_circ_287167,RMVar_hsa_circ_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_136375,RMVar_hsa_circ_348380,RMVar_hsa_circ_365992,RMVar_hsa_circ_46680,RMVar_hsa_circ_304820,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_371865,RMVar_hsa_circ_59942,RMVar_hsa_circ_49077,RMVar_hsa_circ_89708,RMVar_hsa_circ_82305,RMVar_hsa_circ_92765,RMVar_hsa_circ_353270,RMVar_hsa_circ_136379,RMVar_hsa_circ_136380,RMVar_hsa_circ_136381,RMVar_hsa_circ_313505,RMVar_hsa_circ_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,RMVar_hsa_circ_321596,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_370035,RMVar_hsa_circ_106731,RMVar_hsa_circ_136388,RMVar_hsa_circ_136389,RMVar_hsa_circ_83175,RMVar_hsa_circ_278469,RMVar_hsa_circ_351449,RMVar_hsa_circ_85902,RMVar_hsa_circ_136390,RMVar_hsa_circ_136391,RMVar_hsa_circ_136392 93756 RMVar_ID_93756 Human_SNP_ID_34394072 m1A Human chr1 + 154255222 154255222 154255222 ACTTCTAGCATCCCCCCTCTCAATGAAACGGTATCTGCAGCTTCCTTACTGACGACAACCAATCA ACTTCTAGCATCCCCCCTCTCAATGAAACGGTGTCTGCAGCTTCCTTACTGACGACAACCAATCA A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154255129..154255349 26863196 MeRIP-seq:(Medium) rs1291662868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1412421,Human_RBP_ID_1726138,Human_RBP_ID_5536556,Human_RBP_ID_8286087,Human_RBP_ID_10591680,Human_RBP_ID_17212639,Human_RBP_ID_17330481,Human_RBP_ID_17446391,Human_RBP_ID_24556355,Human_RBP_ID_27388583 Human_Splice_Rec_133906,Human_Splice_Rec_133952,Human_Splice_Rec_133998,Human_Splice_Rec_134094,Human_Splice_Rec_134174,Human_Splice_Rec_134200 RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_11572,RMVar_hsa_circ_49077,RMVar_hsa_circ_89708,RMVar_hsa_circ_82305,RMVar_hsa_circ_353270,RMVar_hsa_circ_136379,RMVar_hsa_circ_136381,RMVar_hsa_circ_23121,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_106731,RMVar_hsa_circ_136389,RMVar_hsa_circ_351449,RMVar_hsa_circ_85902,RMVar_hsa_circ_136392,RMVar_hsa_circ_274170,RMVar_hsa_circ_98499,RMVar_hsa_circ_136394,RMVar_hsa_circ_106489,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_324255,RMVar_hsa_circ_136398,RMVar_hsa_circ_321484,RMVar_hsa_circ_136399,RMVar_hsa_circ_136400,RMVar_hsa_circ_136401,RMVar_hsa_circ_116719,RMVar_hsa_circ_65135,RMVar_hsa_circ_118289,RMVar_hsa_circ_136402,RMVar_hsa_circ_108179,RMVar_hsa_circ_136403,RMVar_hsa_circ_136404 93757 RMVar_ID_93757 Human_SNP_ID_34394089 m1A Human chr1 - 154255278 154255278 154255278 TGGTAGTATTTGGAATCTCCTCACTGTGGCTCAAGCCACCCAAGGAGGATGAATGCTGATTGGTT TGGTAGTATTTGGAATCTCCTCACTGTGGCTCCAGCCACCCAAGGAGGATGAATGCTGATTGGTT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:154255176..154255387 26863196 MeRIP-seq:(Medium) rs1165221516 Functional Loss SNV dbSNP153 33..33 33 - - - 93758 RMVar_ID_93758 Human_SNP_ID_34394588 m1A Human chr1 + 154257198 154257198 154257198 CCAGTCTCAATAGTGGCAGTAGCCTGGGCCTCAGCCTAGGCAGCAACTCCACTGTCACAGCCTCG CCAGTCTCAATAGTGGCAGTAGCCTGGGCCTCGGCCTAGGCAGCAACTCCACTGTCACAGCCTCG A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154257150..154257485 32194978 MeRIP-seq:(Medium) rs757730922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327361,Human_RBP_ID_17222820,Human_RBP_ID_17456316,Human_RBP_ID_21880555 Human_Splice_Rec_133911,Human_Splice_Rec_133957,Human_Splice_Rec_134003,Human_Splice_Rec_134099,Human_Splice_Rec_134179,Human_Splice_Rec_134205,Human_Splice_Rec_134215,Human_Splice_Rec_134221,Human_Splice_Rec_134237 RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_11572,RMVar_hsa_circ_49077,RMVar_hsa_circ_89708,RMVar_hsa_circ_82305,RMVar_hsa_circ_136379,RMVar_hsa_circ_136381,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_106731,RMVar_hsa_circ_136389,RMVar_hsa_circ_351449,RMVar_hsa_circ_85902,RMVar_hsa_circ_136392,RMVar_hsa_circ_274170,RMVar_hsa_circ_98499,RMVar_hsa_circ_136394,RMVar_hsa_circ_106489,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_324255,RMVar_hsa_circ_136398,RMVar_hsa_circ_136400,RMVar_hsa_circ_136401,RMVar_hsa_circ_83774,RMVar_hsa_circ_126027,RMVar_hsa_circ_118289,RMVar_hsa_circ_108179,RMVar_hsa_circ_136403,RMVar_hsa_circ_136404,RMVar_hsa_circ_136406,RMVar_hsa_circ_353883,RMVar_hsa_circ_136407 93759 RMVar_ID_93759 Human_SNP_ID_34395023 m1A Human chr1 + 154259027 154259027 154259027 GATGACTTGCAGATGCTTCAGACAAGATTTCCATTGGTGAGTATGTGGGATAGAGCTTTGGAAAA GATGACTTGCAGATGCTTCAGACAAGATTTCCGTTGGTGAGTATGTGGGATAGAGCTTTGGAAAA A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154258964..154259769 32194978 MeRIP-seq:(Medium) rs774825218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1726159,Human_RBP_ID_10591842,Human_RBP_ID_19039253,Human_RBP_ID_22847381 Human_Splice_Rec_133914,Human_Splice_Rec_133915,Human_Splice_Rec_133960,Human_Splice_Rec_133961,Human_Splice_Rec_134006,Human_Splice_Rec_134007,Human_Splice_Rec_134102,Human_Splice_Rec_134103,Human_Splice_Rec_134182,Human_Splice_Rec_134183,Human_Splice_Rec_134208,Human_Splice_Rec_134209,Human_Splice_Rec_134224,Human_Splice_Rec_134225,Human_Splice_Rec_134240,Human_Splice_Rec_134241,Human_Splice_Rec_134257,Human_Splice_Rec_134263 RMVar_hsa_circ_356443,RMVar_hsa_circ_50165,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_11572,RMVar_hsa_circ_49077,RMVar_hsa_circ_89708,RMVar_hsa_circ_82305,RMVar_hsa_circ_136379,RMVar_hsa_circ_136381,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_106731,RMVar_hsa_circ_136389,RMVar_hsa_circ_85902,RMVar_hsa_circ_136392,RMVar_hsa_circ_98499,RMVar_hsa_circ_106489,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_324255,RMVar_hsa_circ_136398,RMVar_hsa_circ_136400,RMVar_hsa_circ_136401,RMVar_hsa_circ_86658,RMVar_hsa_circ_83774,RMVar_hsa_circ_126027,RMVar_hsa_circ_118289,RMVar_hsa_circ_136404,RMVar_hsa_circ_136406,RMVar_hsa_circ_127313,RMVar_hsa_circ_106934,RMVar_hsa_circ_136407,RMVar_hsa_circ_371668,RMVar_hsa_circ_136408,RMVar_hsa_circ_136409,RMVar_hsa_circ_272021,RMVar_hsa_circ_101381,RMVar_hsa_circ_111655,RMVar_hsa_circ_96950,RMVar_hsa_circ_136411,RMVar_hsa_circ_136413,RMVar_hsa_circ_136415,RMVar_hsa_circ_66134,RMVar_hsa_circ_136414,RMVar_hsa_circ_136412,RMVar_hsa_circ_136410 93760 RMVar_ID_93760 Human_SNP_ID_34395523 m1A Human chr1 - 154260980 154260980 154260980 GGGTTCAGGAATGTCTGCTGCGTGGTATGGTGAGTCTGCGTCTGGTTCTGTTGGGGTTGGGCCAA GGGTTCAGGAATGTCTGCTGCGTGGTATGGTGGGTCTGCGTCTGGTTCTGTTGGGGTTGGGCCAA T C lnc-C1orf43-4 RNACentral:URS00008B58D2 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154259967..154260979 32194978 MeRIP-seq:(Medium) rs146701910 Functional Loss SNV dbSNP153 33..33 33 - - - 93761 RMVar_ID_93761 Human_SNP_ID_34395556 m1A Human chr1 - 154261097 154261097 154261097 GACCAAAGCCAGGTACTCACAGGGAACACAGCAGGCCCATACTGGAAGGTGCTGGGGAGGCCCGG GACCAAAGCCAGGTACTCACAGGGAACACAGCCGGCCCATACTGGAAGGTGCTGGGGAGGCCCGG T G lnc-C1orf43-4 RNACentral:URS00008B58D2 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:154261051..154261100 26863196 MeRIP-seq:(Medium) rs1287651067 Functional Loss SNV dbSNP153 33..33 33 - - - 93762 RMVar_ID_93762 Human_SNP_ID_34398546 m1A Human chr1 + 154272701 154272694 154272702 CCCGTCTGCGAATGGACCACTGGAGGGGTTCAAAGGTTCGCGTCCCAGTACGGGAATGAGCCTCT CCCGTCTGCGAATGGACCACTGGAGG________GGTTCGCGTCCCAGTACGGGAATGAGCCTCT GGGTTCAAA G HAX1 Ensembl:ENSG00000143575 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154272626..154272725 26863196 MeRIP-seq:(Medium) rs1380402974 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_745095,Human_RBP_ID_1412463,Human_RBP_ID_3996001,Human_RBP_ID_5311825,Human_RBP_ID_8286142,Human_RBP_ID_8755124,Human_RBP_ID_22023839,Human_RBP_ID_22427536,Human_RBP_ID_26311865 Human_Splice_Rec_134283,Human_Splice_Rec_134295,Human_Splice_Rec_134307,Human_Splice_Rec_134319,Human_Splice_Rec_134331,Human_Splice_Rec_134341,Human_Splice_Rec_134345,Human_Splice_Rec_134355 93763 RMVar_ID_93763 Human_SNP_ID_34398651 m1A Human chr1 + 154273021 154273017 154273021 ATGCAACAGGGACCCGGGCGGGGAAGACCGTGAGGGTCTGGGGAATAAGACAGTGAGCAAGTGAG ATGCAACAGGGACCCGGGCGGGGAAGACC____GGGTCTGGGGAATAAGACAGTGAGCAAGTGAG CGTGA C HAX1 Ensembl:ENSG00000143575 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154273019..154273092 26863196 MeRIP-seq:(Medium) rs1311152096 Functional Loss DEL dbSNP153 30..33 33 - - - 93764 RMVar_ID_93764 Human_SNP_ID_34398861 m1A Human chr1 - 154273470 154273470 154273470 GTATCCCTCCTCCTGGGCTGAAGCTGAAGCCGAAGCCAAATTCCTCAGGGGGGTGCTGAGGACTA GTATCCCTCCTCCTGGGCTGAAGCTGAAGCCGGAGCCAAATTCCTCAGGGGGGTGCTGAGGACTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154273326..154273600 32194978 MeRIP-seq:(Medium) rs1162822393 Functional Loss SNV dbSNP153 33..33 33 - - - 93765 RMVar_ID_93765 Human_SNP_ID_34398917 m1A Human chr1 + 154273622 154273611 154273623 ATCCTCCTGGTGTGTGGCTTTCCCTAAGGGGCAACCTGTGGTTTCTGGTGGGTTGGTGGGTGAAA ATCCTCCTGGTGTGTGGCTTTC____________CCTGTGGTTTCTGGTGGGTTGGTGGGTGAAA CCCTAAGGGGCAA C HAX1 Ensembl:ENSG00000143575 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154273618..154273739 26863196 MeRIP-seq:(Medium) rs1484850337 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_852934,Human_RBP_ID_19039258,Human_RBP_ID_22023842 RMVar_hsa_circ_39662,RMVar_hsa_circ_108442,RMVar_hsa_circ_136421 93766 RMVar_ID_93766 Human_SNP_ID_34398924 m1A Human chr1 + 154273622 154273622 154273622 ATCCTCCTGGTGTGTGGCTTTCCCTAAGGGGCAACCTGTGGTTTCTGGTGGGTTGGTGGGTGAAA ATCCTCCTGGTGTGTGGCTTTCCCTAAGGGGCGACCTGTGGTTTCTGGTGGGTTGGTGGGTGAAA A G HAX1 Ensembl:ENSG00000143575 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154273618..154273739 26863196 MeRIP-seq:(Medium) rs769751533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_852934,Human_RBP_ID_19039258,Human_RBP_ID_22023842 RMVar_hsa_circ_39662,RMVar_hsa_circ_108442,RMVar_hsa_circ_136421 93767 RMVar_ID_93767 Human_SNP_ID_34399287 m1A Human chr1 + 154274999 154274999 154274999 TATGGACCCCCATCCTAGAACCAGAGAGGACAATGGTAAGTCTGGAGGAAGGGGAAGTTTACCAG TATGGACCCCCATCCTAGAACCAGAGAGGACAGTGGTAAGTCTGGAGGAAGGGGAAGTTTACCAG A G HAX1 Ensembl:ENSG00000143575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154274960..154275059 32194978 MeRIP-seq:(Medium) rs1480499507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855284,Human_RBP_ID_1412479 Human_Splice_Rec_134288,Human_Splice_Rec_134289,Human_Splice_Rec_134300,Human_Splice_Rec_134301,Human_Splice_Rec_134312,Human_Splice_Rec_134313,Human_Splice_Rec_134324,Human_Splice_Rec_134325,Human_Splice_Rec_134334,Human_Splice_Rec_134335,Human_Splice_Rec_134344,Human_Splice_Rec_134350,Human_Splice_Rec_134351,Human_Splice_Rec_134358,Human_Splice_Rec_134359,Human_Splice_Rec_134368,Human_Splice_Rec_134369,Human_Splice_Rec_134374,Human_Splice_Rec_134375,Human_Splice_Rec_134380 Human_miRNA_ID_2253920 RMVar_hsa_circ_108442,RMVar_hsa_circ_91557,RMVar_hsa_circ_136421,RMVar_hsa_circ_136422 93768 RMVar_ID_93768 Human_SNP_ID_34399451 m1A Human chr1 - 154275467 154275467 154275467 TTGTCTTTTAACTTACCACCCCTAGGACTGCTATCTGCTTCGTGTCGGGTTACTGTAGTCTCTGT TTGTCTTTTAACTTACCACCCCTAGGACTGCTGTCTGCTTCGTGTCGGGTTACTGTAGTCTCTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154275365..154275515 26863196 MeRIP-seq:(Medium) rs1196857360 Functional Loss SNV dbSNP153 33..33 33 - - - 93769 RMVar_ID_93769 Human_SNP_ID_34399519 m1A Human chr1 - 154275683 154275683 154275683 GAGGGTTAACAAGGCTACCGGGACCGGAACCAACGTCCCAGGAATAAGTCCAGGATGGAAAAGGC GAGGGTTAACAAGGCTACCGGGACCGGAACCAGCGTCCCAGGAATAAGTCCAGGATGGAAAAGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:154275651..154275800 26863196 MeRIP-seq:(Medium) rs756399040 Functional Loss SNV dbSNP153 33..33 33 - - - 93770 RMVar_ID_93770 Human_SNP_ID_34412624 m1A Human chr1 - 154325596 154325596 154325596 CGGCTCGGCTCCCCACGGGCTCCCGCCCCCCCAGCTGCGGCCCCGCTCCCCCGGGGCCTCGGCCC CGGCTCGGCTCCCCACGGGCTCCCGCCCCCCCCGCTGCGGCCCCGCTCCCCCGGGGCCTCGGCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:154325561..154325983;chr1:154325554..154325672 26863196 MeRIP-seq:(Medium) rs1319445939 Functional Loss SNV dbSNP153 33..33 33 - - - 93771 RMVar_ID_93771 Human_SNP_ID_34412647 m1A Human chr1 + 154325624 154325624 154325624 CAGCTGGGGGGGCGGGAGCCCGTGGGGAGCCGAGCCGAGCGCCCCCCGCCCCAGCCCCCGGCATG CAGCTGGGGGGGCGGGAGCCCGTGGGGAGCCGCGCCGAGCGCCCCCCGCCCCAGCCCCCGGCATG A C ATP8B2 Ensembl:ENSG00000143515 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154325576..154326032 26863196 MeRIP-seq:(Medium) rs898764077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745079,Human_RBP_ID_3328578,Human_RBP_ID_4073043,Human_RBP_ID_5234361,Human_RBP_ID_8052739,Human_RBP_ID_17668239,Human_RBP_ID_23206123 Human_Splice_Rec_134411,Human_Splice_Rec_134433 Human_miRNA_ID_1229852 93772 RMVar_ID_93772 Human_SNP_ID_34442558 m1A Human chr1 - 154442450 154442450 154442450 GCCGGCCTCCACCTGTCCCACTCAGACCACCCACCCACACACGTGTCGGCCTCACCAAGCAGCTC GCCGGCCTCCACCTGTCCCACTCAGACCACCCGCCCACACACGTGTCGGCCTCACCAAGCAGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154442217..154442491 26863196 MeRIP-seq:(Medium) rs1415942414 Functional Loss SNV dbSNP153 33..33 33 - - - 93773 RMVar_ID_93773 Human_SNP_ID_34446423 m1A Human chr1 + 154456757 154456757 154456757 CCGAGAACCTCAAGCGGACACGCTTGGCAGGCAACACAGATCGTCACCAGCAAGTAGATGGCAAT CCGAGAACCTCAAGCGGACACGCTTGGCAGGCCACACAGATCGTCACCAGCAAGTAGATGGCAAT A C IL6R Ensembl:ENSG00000160712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154456756..154456880 26863196 MeRIP-seq:(Medium) rs1236395007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268328 93774 RMVar_ID_93774 Human_SNP_ID_34470060 m1A Human chr1 - 154550396 154550396 154550396 ATCACCCTTCCTCCCTCCCCAGGCACCACTGGACCAATTACCTTTGAATGCTGTATTTGGATCTC ATCACCCTTCCTCCCTCCCCAGGCACCACTGGGCCAATTACCTTTGAATGCTGTATTTGGATCTC T C UBE2Q1 Ensembl:ENSG00000160714 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154550347..154550486 26863196 MeRIP-seq:(Medium) rs1427807226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327510,Human_RBP_ID_745336,Human_RBP_ID_971483,Human_RBP_ID_9356901,Human_RBP_ID_10592593,Human_RBP_ID_18552269,Human_RBP_ID_18928631,Human_RBP_ID_27168739,Human_RBP_ID_27388660 Human_Splice_Rec_134780,Human_Splice_Rec_134788 Human_miRNA_ID_244892,Human_miRNA_ID_247395,Human_miRNA_ID_310249,Human_miRNA_ID_1562588 93775 RMVar_ID_93775 Human_SNP_ID_34470215 m1A Human chr1 + 154550910 154550910 154550910 GAAGTGAAAACCTGGGTGTGGCAAGTGTCCGAATCTCCTGAGTCCTGGCTCCAGCCTCACCGTTT GAAGTGAAAACCTGGGTGTGGCAAGTGTCCGAGTCTCCTGAGTCCTGGCTCCAGCCTCACCGTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154550908..154551025 26863196 MeRIP-seq:(Medium) rs1439324656 Functional Loss SNV dbSNP153 33..33 33 - - - 93776 RMVar_ID_93776 Human_SNP_ID_34478910 m1A Human chr1 + 154582567 154582567 154582567 AATTCAGGGATGCCTCGCTCTCTTCCTACAACAGAAACTGAATACTACAGGCTTGCTAGATAAGA AATTCAGGGATGCCTCGCTCTCTTCCTACAACGGAAACTGAATACTACAGGCTTGCTAGATAAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154582517..154582595 26863196 MeRIP-seq:(Medium) rs1379972914 Functional Loss SNV dbSNP153 33..33 33 - - - 93777 RMVar_ID_93777 Human_SNP_ID_34479060 m1A Human chr1 + 154583206 154583202 154583206 GCCTCAGTAGTCCTCCTGAGTGTGTCTAGCTGACTGTTATCGAGGGACACGTAAAAGCAGCATCA GCCTCAGTAGTCCTCCTGAGTGTGTCTAG____CTGTTATCGAGGGACACGTAAAAGCAGCATCA GCTGA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154583155..154583504 32194978 MeRIP-seq:(Medium) rs1230354507 Functional Loss DEL dbSNP153 30..33 33 - - - 93778 RMVar_ID_93778 Human_SNP_ID_34480943 m1A Human chr1 - 154589867 154589867 154589867 CCAGATAGCCATGCTGAGCCACCGGTGCTTCAACACTCTGACTAACAGCTTCCAGCCCTCCTTGC CCAGATAGCCATGCTGAGCCACCGGTGCTTCAGCACTCTGACTAACAGCTTCCAGCCCTCCTTGC T C ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154589421..154589866 32194978 MeRIP-seq:(Medium) rs370898628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327609,Human_RBP_ID_1412577,Human_RBP_ID_1726272,Human_RBP_ID_8735357,Human_RBP_ID_9266383,Human_RBP_ID_10592990,Human_RBP_ID_17330543,Human_RBP_ID_17446486,Human_RBP_ID_18552315,Human_RBP_ID_22427541 Human_Splice_Rec_134884,Human_Splice_Rec_134912,Human_Splice_Rec_134940,Human_Splice_Rec_134992,Human_Splice_Rec_135020,Human_Splice_Rec_135048,Human_Splice_Rec_135076,Human_Splice_Rec_135104,Human_Splice_Rec_135128,Human_Splice_Rec_135154 Human_miRNA_ID_2976029 RMVar_hsa_circ_127324,RMVar_hsa_circ_23411,RMVar_hsa_circ_105169,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_118402,RMVar_hsa_circ_136444,RMVar_hsa_circ_136446,RMVar_hsa_circ_136445,RMVar_hsa_circ_365332,RMVar_hsa_circ_43148,RMVar_hsa_circ_58192,RMVar_hsa_circ_275867,RMVar_hsa_circ_136449,RMVar_hsa_circ_17336 93779 RMVar_ID_93779 Human_SNP_ID_34483165 m1A Human chr1 + 154597940 154597940 154597940 TGTGGTGACGGGGCTCTTCCCAGAAAAGAAGGATGTGGCTGAAGGGGTGGGGGTCTGGGACTCTG TGTGGTGACGGGGCTCTTCCCAGAAAAGAAGGGTGTGGCTGAAGGGGTGGGGGTCTGGGACTCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154597890..154598012 26863196 MeRIP-seq:(Medium) rs756311131 Functional Loss SNV dbSNP153 33..33 33 - - - 93780 RMVar_ID_93780 Human_SNP_ID_34484156 m1A Human chr1 - 154601491 154601491 154601491 TGAAACCGCTCCAGCTGCAATCCCTGAGACCAAAAGAAACGCAGAGTTCCTCACCTGTAATATAC TGAAACCGCTCCAGCTGCAATCCCTGAGACCAGAAGAAACGCAGAGTTCCTCACCTGTAATATAC T C ADAR Ensembl:ENSG00000160710 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2229857 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_858053,Human_RBP_ID_8754143,Human_RBP_ID_17221650,Human_RBP_ID_19151593,Human_RBP_ID_21879230,Human_RBP_ID_26311876 Human_miRNA_ID_247398 Clinvar_Rec_531 GWAS_ID_12199,GWAS_ID_12200,GWAS_ID_12201,GWAS_ID_12202,GWAS_ID_12203,GWAS_ID_12204 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203,RMVar_hsa_circ_136455 93781 RMVar_ID_93781 Human_SNP_ID_34484367 m1A Human chr1 - 154602055 154602055 154602055 ACAGAAAGAGGCAGGAACACCCCCTTTGTGGAAAATCGCGGTCTCCACTCAGGCTTGGAACCAGC ACAGAAAGAGGCAGGAACACCCCCTTTGTGGACAATCGCGGTCTCCACTCAGGCTTGGAACCAGC T G ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154602016..154602149 26863196 MeRIP-seq:(Medium) rs1209683504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22113,Human_RBP_ID_3996559,Human_RBP_ID_8735405,Human_RBP_ID_9356921,Human_RBP_ID_18552356,Human_RBP_ID_26309819,Human_RBP_ID_26842752,Human_RBP_ID_27168823 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203 93782 RMVar_ID_93782 Human_SNP_ID_34484566 m1A Human chr1 - 154602583 154602583 154602583 CAGCGGATACTACACCCATCCATTTCAAGGCTATGAGCACAGACAGCTCAGGTACCAGCAGCCTG CAGCGGATACTACACCCATCCATTTCAAGGCTGTGAGCACAGACAGCTCAGGTACCAGCAGCCTG T C ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154602533..154602650 26863196 MeRIP-seq:(Medium) rs754158375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22118,Human_RBP_ID_4074447,Human_RBP_ID_5458541,Human_RBP_ID_9356924,Human_RBP_ID_18187277,Human_RBP_ID_18552363,Human_RBP_ID_26842760 Human_Splice_Rec_134872,Human_Splice_Rec_134900,Human_Splice_Rec_134928,Human_Splice_Rec_134980,Human_Splice_Rec_135008,Human_Splice_Rec_135036,Human_Splice_Rec_135064,Human_Splice_Rec_135092,Human_Splice_Rec_135116,Human_Splice_Rec_135214,Human_Splice_Rec_135216,Human_Splice_Rec_135218,Human_Splice_Rec_135220 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_126815,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203,RMVar_hsa_circ_76145,RMVar_hsa_circ_84571,RMVar_hsa_circ_136457,RMVar_hsa_circ_136458,RMVar_hsa_circ_136459 93783 RMVar_ID_93783 Human_SNP_ID_34484573 m1A Human chr1 - 154602602 154602602 154602602 TTCTGCAGGGGTATTCCCTCAGCGGATACTACACCCATCCATTTCAAGGCTATGAGCACAGACAG TTCTGCAGGGGTATTCCCTCAGCGGATACTACCCCCATCCATTTCAAGGCTATGAGCACAGACAG T G ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154602551..154602650 26863196 MeRIP-seq:(Medium) rs1162214932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1232769,Human_RBP_ID_1412628,Human_RBP_ID_4074447,Human_RBP_ID_5413029,Human_RBP_ID_5432953,Human_RBP_ID_5456366,Human_RBP_ID_5484459,Human_RBP_ID_8043655,Human_RBP_ID_8980417,Human_RBP_ID_9356924,Human_RBP_ID_17330548,Human_RBP_ID_17726590,Human_RBP_ID_18187277,Human_RBP_ID_18552364,Human_RBP_ID_23260402,Human_RBP_ID_26801059 Human_Splice_Rec_134872,Human_Splice_Rec_134900,Human_Splice_Rec_134928,Human_Splice_Rec_134980,Human_Splice_Rec_135008,Human_Splice_Rec_135036,Human_Splice_Rec_135064,Human_Splice_Rec_135092,Human_Splice_Rec_135116,Human_Splice_Rec_135214,Human_Splice_Rec_135216,Human_Splice_Rec_135218,Human_Splice_Rec_135220 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_126815,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203,RMVar_hsa_circ_76145,RMVar_hsa_circ_84571,RMVar_hsa_circ_136457,RMVar_hsa_circ_136458,RMVar_hsa_circ_136459 93784 RMVar_ID_93784 Human_SNP_ID_34486093 m1A Human chr1 + 154608143 154608143 154608143 CACTGGAAGTGGCCCCGGGGCGTCGGCACGGGAAACTCCGCGGGTCTGCGCGCCGGGCCCAAGAT CACTGGAAGTGGCCCCGGGGCGTCGGCACGGGGAACTCCGCGGGTCTGCGCGCCGGGCCCAAGAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154608014..154608200 26863196 MeRIP-seq:(Medium) rs958245319 Functional Loss SNV dbSNP153 33..33 33 - - - 93785 RMVar_ID_93785 Human_SNP_ID_34490618 m1A Human chr1 + 154627896 154627896 154627896 CACTTCCTCGGGACACGGCCGGACACCCGGAGACTGCCAGTGCGGCCGCGACCCTCCCCCCACCC CACTTCCTCGGGACACGGCCGGACACCCGGAGGCTGCCAGTGCGGCCGCGACCCTCCCCCCACCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:154627810..154627939 26863196 MeRIP-seq:(Medium) rs6426859 Functional Loss SNV dbSNP153 33..33 33 - - - 93786 RMVar_ID_93786 Human_SNP_ID_34490639 m1A Human chr1 - 154627918 154627918 154627918 GAGAAGGCTACGTGGTGGGGGAGGGTGGGGGGAGGGTCGCGGCCGCACTGGCAGTCTCCGGGTGT GAGAAGGCTACGTGGTGGGGGAGGGTGGGGGGGGGGTCGCGGCCGCACTGGCAGTCTCCGGGTGT T C ADAR Ensembl:ENSG00000160710 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154627806..154627975 26863196 MeRIP-seq:(Medium) rs749763161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25396,Human_RBP_ID_224364,Human_RBP_ID_745329,Human_RBP_ID_4073055,Human_RBP_ID_5312686,Human_RBP_ID_5519187,Human_RBP_ID_18415071,Human_RBP_ID_26311878,Human_RBP_ID_26767564 Human_Splice_Rec_134927,Human_Splice_Rec_135217 93787 RMVar_ID_93787 Human_SNP_ID_34560834 m1A Human chr1 - 154926420 154926420 154926420 TCCAGTGGTTTCGGGAGGCCTATGGGGCCGTGACGCAGACGGTCCGCGTTGTAGCGTTGGAGCAG TCCAGTGGTTTCGGGAGGCCTATGGGGCCGTGGCGCAGACGGTCCGCGTTGTAGCGTTGGAGCAG T C PMVK Ensembl:ENSG00000163344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:154926307..154926500;chr1:154926310..154926500;chr1:154926292..154926524 26863196 MeRIP-seq:(Medium) rs372574645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327640 Human_Splice_Rec_135290,Human_Splice_Rec_135291 RMVar_hsa_circ_108951,RMVar_hsa_circ_136466 93788 RMVar_ID_93788 Human_SNP_ID_34563317 m1A Human chr1 + 154936684 154936684 154936684 GTACCAGCCGCGGGGCGCCTCCCAGCGGGGCCATGGGGCCGCCACGCCTCGCGATGCCTGAAGCT GTACCAGCCGCGGGGCGCCTCCCAGCGGGGCCCTGGGGCCGCCACGCCTCGCGATGCCTGAAGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:154936539..154936950;chr1:154936527..154936918 26863196 MeRIP-seq:(Medium) rs763698153 Functional Loss SNV dbSNP153 33..33 33 - - - 93789 RMVar_ID_93789 Human_SNP_ID_34563318 m1A Human chr1 + 154936684 154936684 154936684 GTACCAGCCGCGGGGCGCCTCCCAGCGGGGCCATGGGGCCGCCACGCCTCGCGATGCCTGAAGCT GTACCAGCCGCGGGGCGCCTCCCAGCGGGGCCTTGGGGCCGCCACGCCTCGCGATGCCTGAAGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:154936539..154936950;chr1:154936527..154936918 26863196 MeRIP-seq:(Medium) rs763698153 Functional Loss SNV dbSNP153 33..33 33 - - - 93790 RMVar_ID_93790 Human_SNP_ID_34563331 m1A Human chr1 - 154936706 154936706 154936706 TTTAGGGGTAGGGAGAAGTGTCAGCTTCAGGCATCGCGAGGCGTGGCGGCCCCATGGCCCCGCTG TTTAGGGGTAGGGAGAAGTGTCAGCTTCAGGCCTCGCGAGGCGTGGCGGCCCCATGGCCCCGCTG T G PMVK Ensembl:ENSG00000163344 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154936549..154936750 26863196 MeRIP-seq:(Medium) rs780530219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327642,Human_RBP_ID_4073057 93791 RMVar_ID_93791 Human_SNP_ID_34563396 m1A Human chr1 + 154936925 154936925 154936925 ACGCGGAGAGAAAGGCGGTTCCTTCACAGAGCAGCCTCCCCTCGTGAAGCTCCCCCACCCGAACT ACGCGGAGAGAAAGGCGGTTCCTTCACAGAGCGGCCTCCCCTCGTGAAGCTCCCCCACCCGAACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154936877..154936948 26863196 MeRIP-seq:(Medium) rs1022418566 Functional Loss SNV dbSNP153 33..33 33 - - - 93792 RMVar_ID_93792 Human_SNP_ID_34565258 m1A Human chr1 - 154944827 154944827 154944827 AAAAGGCCTTAGCTGGACCTGCGTTGCCGTCTATGCAAATGCATGCAAATACTCCAGGCCCTGGG AAAAGGCCTTAGCTGGACCTGCGTTGCCGTCTGTGCAAATGCATGCAAATACTCCAGGCCCTGGG T C PBXIP1 Ensembl:ENSG00000163346 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154944776..154944842 26863196 MeRIP-seq:(Medium) rs1324452731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327655,Human_RBP_ID_5109696,Human_RBP_ID_17647084,Human_RBP_ID_18552380,Human_RBP_ID_21879231 Human_miRNA_ID_351035,Human_miRNA_ID_1288864,Human_miRNA_ID_2092617,Human_miRNA_ID_2734899 RMVar_hsa_circ_99558,RMVar_hsa_circ_136468 93793 RMVar_ID_93793 Human_SNP_ID_34565600 m1A Human chr1 + 154945870 154945870 154945870 TTGCCGCACTGGGGCTAGCTCTGTGCCAAAGAAAGTCAGGCCCTCCTGCCGGGCACACTCGTCCA TTGCCGCACTGGGGCTAGCTCTGTGCCAAAGAGAGTCAGGCCCTCCTGCCGGGCACACTCGTCCA A G NONHSAG003032.2 RNACentral:URS00008B1FF6 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154945784..154945925 26863196 MeRIP-seq:(Medium) rs766574634 Functional Loss SNV dbSNP153 33..33 33 - - - 93794 RMVar_ID_93794 Human_SNP_ID_34565683 m1A Human chr1 - 154946085 154946085 154946085 GGGCAGGCCAAGGGTGGAGGAGTCGGGGAGCAAGAAGGAGGGCAAGCGACAGGGCCCGAAGGAAC GGGCAGGCCAAGGGTGGAGGAGTCGGGGAGCACGAAGGAGGGCAAGCGACAGGGCCCGAAGGAAC T G PBXIP1 Ensembl:ENSG00000163346 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:154945826..154946825;chr1:154945951..154946775;chr1:154945951..154947144 26863196 MeRIP-seq:(Medium) rs144596543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934080,Human_RBP_ID_5086222,Human_RBP_ID_5136379,Human_RBP_ID_9412622,Human_RBP_ID_22026464,Human_RBP_ID_22751218,Human_RBP_ID_26311879,Human_RBP_ID_27800854 Human_miRNA_ID_2443352 RMVar_hsa_circ_99558,RMVar_hsa_circ_136468 93795 RMVar_ID_93795 Human_SNP_ID_34567049 m1A Human chr1 - 154951336 154951336 154951336 GGAGCCTCCTGGCCCAGGAGACACAGTAGTCCAGGGAGACCTGCAGGAGACCACCGTGGTGACAG GGAGCCTCCTGGCCCAGGAGACACAGTAGTCCTGGGAGACCTGCAGGAGACCACCGTGGTGACAG T A PBXIP1 Ensembl:ENSG00000163346 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154951202..154951565 26863196 MeRIP-seq:(Medium) rs967607480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743992,Human_RBP_ID_3936713,Human_RBP_ID_5333743,Human_RBP_ID_9359397,Human_RBP_ID_22428598 Human_Splice_Rec_135298,Human_Splice_Rec_135318,Human_Splice_Rec_135338,Human_Splice_Rec_135350,Human_Splice_Rec_135366,Human_Splice_Rec_135376 Human_miRNA_ID_2508507,Human_miRNA_ID_2541056,Human_miRNA_ID_2542949,Human_miRNA_ID_2544806,Human_miRNA_ID_2546647,Human_miRNA_ID_2548516,Human_miRNA_ID_2550380,Human_miRNA_ID_2555781,Human_miRNA_ID_2557663,Human_miRNA_ID_2588077 RMVar_hsa_circ_99558,RMVar_hsa_circ_136468,RMVar_hsa_circ_349446,RMVar_hsa_circ_136469 93796 RMVar_ID_93796 Human_SNP_ID_34567205 m1A Human chr1 - 154951865 154951863 154951865 CCGGCATCCAGGATGGACCCAGAATCTGAGAGAGCCCTGCAGGCCCCTCACAGCCCCTCCAAGAC CCGGCATCCAGGATGGACCCAGAATCTGAGAG__CCCTGCAGGCCCCTCACAGCCCCTCCAAGAC GCT G PBXIP1 Ensembl:ENSG00000163346 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154951767..154951949 26863196 MeRIP-seq:(Medium) rs763923030 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3936714 Human_Splice_Rec_135294,Human_Splice_Rec_135295,Human_Splice_Rec_135314,Human_Splice_Rec_135315,Human_Splice_Rec_135334,Human_Splice_Rec_135335,Human_Splice_Rec_135362,Human_Splice_Rec_135363,Human_Splice_Rec_135374 RMVar_hsa_circ_99558,RMVar_hsa_circ_136468,RMVar_hsa_circ_349446,RMVar_hsa_circ_136469 93797 RMVar_ID_93797 Human_SNP_ID_34567342 m1A Human chr1 + 154952319 154952319 154952319 CTGGGTGCCCACGGGTCACAGTTATGCCTCCCAGGGTGTCCCTGCAGCTGCCCTCTCAACTGGAC CTGGGTGCCCACGGGTCACAGTTATGCCTCCCCGGGTGTCCCTGCAGCTGCCCTCTCAACTGGAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154952310..154952616 26863196 MeRIP-seq:(Medium) rs1419687173 Functional Loss SNV dbSNP153 33..33 33 - - - 93798 RMVar_ID_93798 Human_SNP_ID_34568135 m1A Human chr1 - 154956058 154956058 154956058 ACCGAAGCAAGAGCTGGTTCAGGTAATGCCTTAGCTGGGAAGGGGTCCACAGATTCGCTTTGAAG ACCGAAGCAAGAGCTGGTTCAGGTAATGCCTTGGCTGGGAAGGGGTCCACAGATTCGCTTTGAAG T C PBXIP1 Ensembl:ENSG00000163346 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154956051..154956125 26863196 MeRIP-seq:(Medium) rs1006165746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19035455 RMVar_hsa_circ_99558,RMVar_hsa_circ_136468 93799 RMVar_ID_93799 Human_SNP_ID_34568442 m1A Human chr1 + 154957234 154957232 154957235 AAAAACAGCAACAGATAAATGGGGCAAACAGAACAACAAACACAAGAGTTGAGCAGCGGGGTGGG AAAAACAGCAACAGATAAATGGGGCAAACAG___AACAAACACAAGAGTTGAGCAGCGGGGTGGG GAAC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154957183..154957508 26863196 MeRIP-seq:(Medium) rs964601359 Functional Loss DEL dbSNP153 32..34 33 - - - 93800 RMVar_ID_93800 Human_SNP_ID_34568471 m1A Human chr1 + 154957307 154957307 154957307 GTTGCCATCTACGCCGTTTTAGTGTGAGGGACACTGGGAACGATGCCCAGAGGCTGCTCTCCTCC GTTGCCATCTACGCCGTTTTAGTGTGAGGGACGCTGGGAACGATGCCCAGAGGCTGCTCTCCTCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:154957151..154957400 26863196 MeRIP-seq:(Medium) rs1266408082 Functional Loss SNV dbSNP153 33..33 33 - - - 93801 RMVar_ID_93801 Human_SNP_ID_34568845 m1A Human chr1 + 154958772 154958772 154958772 GGAGAGACATGTGCACTTCCCTGGGCCACTTCACCAGCGTCACCCATCGTTAGCAGCCACCAGCT GGAGAGACATGTGCACTTCCCTGGGCCACTTCCCCAGCGTCACCCATCGTTAGCAGCCACCAGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154958721..154958923 26863196 MeRIP-seq:(Medium) rs1288922950 Functional Loss SNV dbSNP153 33..33 33 - - - 93802 RMVar_ID_93802 Human_SNP_ID_34569817 m1A Human chr1 - 154961576 154961576 154961576 CGCCGCTGCCGCTAACCCGGGTCCCCCACTCCATGGCCGCCTCGGCGCCGCCCCCACCGGACAAG CGCCGCTGCCGCTAACCCGGGTCCCCCACTCCTTGGCCGCCTCGGCGCCGCCCCCACCGGACAAG T A PYGO2 Ensembl:ENSG00000163348 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154961527..154961721 26863196 MeRIP-seq:(Medium) rs1468454272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4082164 93803 RMVar_ID_93803 Human_SNP_ID_34569818 m1A Human chr1 - 154961576 154961576 154961576 CGCCGCTGCCGCTAACCCGGGTCCCCCACTCCATGGCCGCCTCGGCGCCGCCCCCACCGGACAAG CGCCGCTGCCGCTAACCCGGGTCCCCCACTCCGTGGCCGCCTCGGCGCCGCCCCCACCGGACAAG T C PYGO2 Ensembl:ENSG00000163348 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154961527..154961721 26863196 MeRIP-seq:(Medium) rs1468454272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4082164 93804 RMVar_ID_93804 Human_SNP_ID_34569840 m1A Human chr1 - 154961626 154961626 154961626 CCTGACACCCCTTCTGGGCGATGGTGCAGCCCAAGGGCGCCTCCATCCCCCGCCGCTGCCGCTAA CCTGACACCCCTTCTGGGCGATGGTGCAGCCCGAGGGCGCCTCCATCCCCCGCCGCTGCCGCTAA T C PYGO2 Ensembl:ENSG00000163348 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:154961576..154961733 26863196 MeRIP-seq:(Medium) rs1398734060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074451,Human_RBP_ID_5484478,Human_RBP_ID_9319174 93805 RMVar_ID_93805 Human_SNP_ID_34570159 m1A Human chr1 - 154962469 154962458 154962469 CAGTTCCTGAGTACCTTCTACAGGCCCGGCCCAGCCTAGGCCCGGGGTGGCCACACCACAGCAAG CAGTTCCTGAGTACCTTCTACAGGCCCGGCCC___________GGGGTGGCCACACCACAGCAAG CGGGCCTAGGCT C SHC1,PYGO2 Ensembl:ENSG00000160691,Ensembl:ENSG00000163348 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:154962223..154962525;chr1:154962323..154962575 32194978 MeRIP-seq:(Medium) rs949813475 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_327696,Human_RBP_ID_26386481 Human_miRNA_ID_2673919,Human_miRNA_ID_2673920,Human_miRNA_ID_2924675,Human_miRNA_ID_2924676 RMVar_hsa_circ_114089,RMVar_hsa_circ_93581,RMVar_hsa_circ_123316,RMVar_hsa_circ_136470,RMVar_hsa_circ_136472,RMVar_hsa_circ_91316,RMVar_hsa_circ_136473,RMVar_hsa_circ_136471 93806 RMVar_ID_93806 Human_SNP_ID_34570444 m1A Human chr1 - 154963601 154963601 154963601 AGCCTGGGTGAGAATCCTGCCTCTCCCCAAACATTAATCACCAAAGTATTAATGTACAGAGTGGC AGCCTGGGTGAGAATCCTGCCTCTCCCCAAACGTTAATCACCAAAGTATTAATGTACAGAGTGGC T C SHC1,PYGO2 Ensembl:ENSG00000160691,Ensembl:ENSG00000163348 Protein coding,Protein coding 3'UTR,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154963551..154963800 32194978 MeRIP-seq:(Medium) rs1300989017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5519188,Human_RBP_ID_8228627,Human_RBP_ID_17330561,Human_RBP_ID_17675214,Human_RBP_ID_17726661,Human_RBP_ID_27388789 Human_Splice_Rec_135385 Human_miRNA_ID_1201124,Human_miRNA_ID_3106080,Human_miRNA_ID_3106081 RMVar_hsa_circ_114089,RMVar_hsa_circ_93581,RMVar_hsa_circ_123316,RMVar_hsa_circ_136470,RMVar_hsa_circ_136472,RMVar_hsa_circ_91316,RMVar_hsa_circ_136473,RMVar_hsa_circ_136471 93807 RMVar_ID_93807 Human_SNP_ID_34570537 m1A Human chr1 + 154963855 154963853 154963856 GTTGCTGTAGACACAGTTCGCTGCCCGCAGAGATGATGGGCAAGTGATTGTCCATGTGGTAGCTG GTTGCTGTAGACACAGTTCGCTGCCCGCAGA___GATGGGCAAGTGATTGTCCATGTGGTAGCTG AGAT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154963804..154963954 26863196 MeRIP-seq:(Medium) rs1334448521 Functional Loss DEL dbSNP153 32..34 33 - - - 93808 RMVar_ID_93808 Human_SNP_ID_34571050 m1A Human chr1 - 154965652 154965652 154965652 CCGGCGGGAGGCTGAGGCACTGCTGCAGCTCAATGGGGACTTCCTGGTACGGGAGAGCACGACCA CCGGCGGGAGGCTGAGGCACTGCTGCAGCTCAGTGGGGACTTCCTGGTACGGGAGAGCACGACCA T C SHC1 Ensembl:ENSG00000160691 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:154965601..154965725 32194978 MeRIP-seq:(Medium) rs141502949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5519189 Human_Splice_Rec_135497 RMVar_hsa_circ_43303,RMVar_hsa_circ_114089,RMVar_hsa_circ_93581,RMVar_hsa_circ_123316,RMVar_hsa_circ_136470,RMVar_hsa_circ_136472,RMVar_hsa_circ_91316,RMVar_hsa_circ_136473,RMVar_hsa_circ_377371,RMVar_hsa_circ_136471,RMVar_hsa_circ_324940,RMVar_hsa_circ_136474 93809 RMVar_ID_93809 Human_SNP_ID_34571101 m1A Human chr1 + 154965776 154965776 154965776 GGGAGGTGGAGGCACGCGAAGAGCATCTTCGAAGGGCTCTGGAAGTATAGAGGGAGGGTGAGGGG GGGAGGTGGAGGCACGCGAAGAGCATCTTCGACGGGCTCTGGAAGTATAGAGGGAGGGTGAGGGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:154965726..154965800 26863196 MeRIP-seq:(Medium) rs1439225757 Functional Loss SNV dbSNP153 33..33 33 - - - 93810 RMVar_ID_93810 Human_SNP_ID_34571155 m1A Human chr1 + 154965928 154965926 154965928 GAACCAAGTAGAAAGGTGGGGATGCAGAGAGGAGAGAGACGAGCACTCACTCATGTCAAACAGGT GAACCAAGTAGAAAGGTGGGGATGCAGAGAG__GAGAGACGAGCACTCACTCATGTCAAACAGGT GGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:154965926..154966050;chr1:154965926..154966075 26863196 MeRIP-seq:(Medium) rs762597104 Functional Loss DEL dbSNP153 32..33 33 - - - 93811 RMVar_ID_93811 Human_SNP_ID_34571299 m1A Human chr1 + 154966321 154966321 154966321 CCCCAGCCCGCCTCCATCCAAGCAACTTACCAATGTAGCTCCCAAGTGGCTGGGGGTCTGGGCAT CCCCAGCCCGCCTCCATCCAAGCAACTTACCAGTGTAGCTCCCAAGTGGCTGGGGGTCTGGGCAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:154966301..154966350 26863196 MeRIP-seq:(Medium) rs77859168 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93812 RMVar_ID_93812 Human_SNP_ID_34571317 m1A Human chr1 + 154966361 154966361 154966361 CCCAAGTGGCTGGGGGTCTGGGCATTGGGTGCAGTGGGTCGAGCAGCCCCTGGAGCGGCTCCTTC CCCAAGTGGCTGGGGGTCTGGGCATTGGGTGCGGTGGGTCGAGCAGCCCCTGGAGCGGCTCCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154966224..154966452 26863196 MeRIP-seq:(Medium) rs750776129 Functional Loss SNV dbSNP153 33..33 33 - - - 93813 RMVar_ID_93813 Human_SNP_ID_34571355 m1A Human chr1 + 154966423 154966423 154966423 TTCCCGAAGCCTCATGTCTACCACCCCCCCCAAGGGGGGTTCCTTCCCCGGGAAGTCATTATAGT TTCCCGAAGCCTCATGTCTACCACCCCCCCCAGGGGGGGTTCCTTCCCCGGGAAGTCATTATAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154966374..154966445 26863196 MeRIP-seq:(Medium) rs1558054538 Functional Loss SNV dbSNP153 33..33 33 - - - 93814 RMVar_ID_93814 Human_SNP_ID_34571960 m1A Human chr1 - 154968590 154968590 154968590 TACCTTAGCCCTGTAGCCGCCCGCTCAGCTCTATCCTGGGGAGGAGTAACCTGAAATTTGCTGGA TACCTTAGCCCTGTAGCCGCCCGCTCAGCTCTGTCCTGGGGAGGAGTAACCTGAAATTTGCTGGA T C SHC1 Ensembl:ENSG00000160691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154968540..154968860 26863196 MeRIP-seq:(Medium) rs150941014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855298,Human_RBP_ID_18966028,Human_RBP_ID_19035462,Human_RBP_ID_27388805 Human_Splice_Rec_135394,Human_Splice_Rec_135395,Human_Splice_Rec_135416,Human_Splice_Rec_135417,Human_Splice_Rec_135433,Human_Splice_Rec_135456,Human_Splice_Rec_135457,Human_Splice_Rec_135480,Human_Splice_Rec_135481,Human_Splice_Rec_135508,Human_Splice_Rec_135509,Human_Splice_Rec_135520,Human_Splice_Rec_135521,Human_Splice_Rec_135536,Human_Splice_Rec_135537,Human_Splice_Rec_135550 Human_miRNA_ID_2256078 RMVar_hsa_circ_43303,RMVar_hsa_circ_93581,RMVar_hsa_circ_136470,RMVar_hsa_circ_91316,RMVar_hsa_circ_136473,RMVar_hsa_circ_317581,RMVar_hsa_circ_331251,RMVar_hsa_circ_136480,RMVar_hsa_circ_58190,RMVar_hsa_circ_136481,RMVar_hsa_circ_346787 93815 RMVar_ID_93815 Human_SNP_ID_34572432 m1A Human chr1 + 154970141 154970141 154970141 AGCTCCCGTGGCGGGTCCACTCCTCGCCCCCAAGCTGGCCCCCTTCCACCCGAGTCCTGCGCCCG AGCTCCCGTGGCGGGTCCACTCCTCGCCCCCAGGCTGGCCCCCTTCCACCCGAGTCCTGCGCCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:154970126..154970150 26863196 MeRIP-seq:(Medium) rs746181295 Functional Loss SNV dbSNP153 33..33 33 - - - 93816 RMVar_ID_93816 Human_SNP_ID_34572450 m1A Human chr1 - 154970179 154970179 154970179 CCCCTCCTCCAGGACATGAACAAGCTGAGTGGAGGCGGCGGGCGCAGGACTCGGGTGGAAGGGGG CCCCTCCTCCAGGACATGAACAAGCTGAGTGGTGGCGGCGGGCGCAGGACTCGGGTGGAAGGGGG T A SHC1 Ensembl:ENSG00000160691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154970005..154970261 26863196 MeRIP-seq:(Medium) rs767189880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3996869,Human_RBP_ID_10593875,Human_RBP_ID_18966033,Human_RBP_ID_22871641 Human_Splice_Rec_135450,Human_Splice_Rec_135474,Human_Splice_Rec_135530,Human_Splice_Rec_135544 RMVar_hsa_circ_43303 93817 RMVar_ID_93817 Human_SNP_ID_34572598 m1A Human chr1 + 154970519 154970519 154970519 GGAGTGGATTGTACTTGGGCTTGGGGGGCAGGAGATCCATAGTTGAGGTGAAAGAGGGGCTGCTG GGAGTGGATTGTACTTGGGCTTGGGGGGCAGGTGATCCATAGTTGAGGTGAAAGAGGGGCTGCTG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:154970501..154970650 26863196 MeRIP-seq:(Medium) rs189263031 Functional Loss SNV dbSNP153 33..33 33 - - - 93818 RMVar_ID_93818 Human_SNP_ID_34573442 m1A Human chr1 + 154973832 154973832 154973832 GGGGAGGCTTTCTGGACAGTCAGACGTGGATTACGGAGGGGGCGTGGCTTCGGAGGGGCGGAGCT GGGGAGGCTTTCTGGACAGTCAGACGTGGATTCCGGAGGGGGCGTGGCTTCGGAGGGGCGGAGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154973831..154974055 26863196 MeRIP-seq:(Medium) rs538019631 Functional Loss SNV dbSNP153 33..33 33 - - - 93819 RMVar_ID_93819 Human_SNP_ID_34573760 m1A Human chr1 + 154974760 154974760 154974760 CTAGCAAACCGAGCGATCATGTCGCACAAACAAATTTACTATTCGGACAAATACGACGACGAGGA CTAGCAAACCGAGCGATCATGTCGCACAAACAGATTTACTATTCGGACAAATACGACGACGAGGA A G CKS1B Ensembl:ENSG00000173207 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:154974651..154974852 26863410 MeRIP-seq:(Medium) rs1467056254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1726341,Human_RBP_ID_4074453 Human_Splice_Rec_135555,Human_Splice_Rec_135559 RMVar_hsa_circ_98035,RMVar_hsa_circ_136483 93820 RMVar_ID_93820 Human_SNP_ID_34576034 m1A Human chr1 - 154984033 154984033 154984033 TTAAGGATCTCATCTCCAACAATGATGATGCCAGCCGTCACGCTGCGCCCCGGAGAAAGTTCAGA TTAAGGATCTCATCTCCAACAATGATGATGCCGGCCGTCACGCTGCGCCCCGGAGAAAGTTCAGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:154983783..154984032 32194978 MeRIP-seq:(Medium) rs1044204334 Functional Loss SNV dbSNP153 33..33 33 - - - 93821 RMVar_ID_93821 Human_SNP_ID_34577943 m1A Human chr1 + 154990413 154990413 154990413 GGCCCTGGGTGAACTGCAGGCACGGCACCCCCAGCTGGAGGCTGTCCTTATGGGCACCCGCCGGA GGCCCTGGGTGAACTGCAGGCACGGCACCCCCGGCTGGAGGCTGTCCTTATGGGCACCCGCCGGA A G FLAD1 Ensembl:ENSG00000160688 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:154990363..154990463 32194978 MeRIP-seq:(Medium) rs947902409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327753,Human_RBP_ID_3996953,Human_RBP_ID_18966036,Human_RBP_ID_27388842 Human_Splice_Rec_135582,Human_Splice_Rec_135602,Human_Splice_Rec_135616,Human_Splice_Rec_135648 Human_miRNA_ID_1355366,Human_miRNA_ID_2682880,Human_miRNA_ID_2682881 RMVar_hsa_circ_136485,RMVar_hsa_circ_100202,RMVar_hsa_circ_58525,RMVar_hsa_circ_110664,RMVar_hsa_circ_88673,RMVar_hsa_circ_107749,RMVar_hsa_circ_136487,RMVar_hsa_circ_136488,RMVar_hsa_circ_315160,RMVar_hsa_circ_351147,RMVar_hsa_circ_136489,RMVar_hsa_circ_136490 93822 RMVar_ID_93822 Human_SNP_ID_34580782 m1A Human chr1 - 155000002 155000002 155000002 GGGAGAGTAGCACGAGTTGGACAAATACCCAGAGAAGGAAGTGTTTACCCTAAGAGAGGAATGAA GGGAGAGTAGCACGAGTTGGACAAATACCCAGTGAAGGAAGTGTTTACCCTAAGAGAGGAATGAA T A lnc-DCST2-2 RNACentral:URS00008B7FB4 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154999839..155000151 26863196 MeRIP-seq:(Medium) rs1439506426 Functional Loss SNV dbSNP153 33..33 33 - - - 93823 RMVar_ID_93823 Human_SNP_ID_34581332 m1A Human chr1 + 155001809 155001809 155001809 TCCCTCCCCGCGGGGCACCGTCACGCGTGGGGAGGGACGCAGGGCGCCCGCAGGCTCAACTCCCC TCCCTCCCCGCGGGGCACCGTCACGCGTGGGGGGGGACGCAGGGCGCCCGCAGGCTCAACTCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155001795..155001864 26863196 MeRIP-seq:(Medium) rs557202657 Functional Loss SNV dbSNP153 33..33 33 - - - 93824 RMVar_ID_93824 Human_SNP_ID_34582398 m1A Human chr1 + 155005725 155005725 155005725 GGGAGAGAACAGTGGGGGAGGAAGGTGGGGACAGGCAGATGGATAGGACCCTGGCATGGGGTGTG GGGAGAGAACAGTGGGGGAGGAAGGTGGGGACGGGCAGATGGATAGGACCCTGGCATGGGGTGTG A G ZBTB7B Ensembl:ENSG00000160685 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155005723..155005875 26863196 MeRIP-seq:(Medium) rs1012941437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1468,Human_RBP_ID_3328599,Human_RBP_ID_18928642 93825 RMVar_ID_93825 Human_SNP_ID_34583152 m1A Human chr1 - 155009034 155009034 155009034 GTCCTCTGACCCTTGGCTAATTCTAGGCCTCCAAGCCCCCCTGGGGCCTGATCTCCCAAGCCAGA GTCCTCTGACCCTTGGCTAATTCTAGGCCTCCGAGCCCCCCTGGGGCCTGATCTCCCAAGCCAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155009029..155009383 26863196 MeRIP-seq:(Medium) rs1405162123 Functional Loss SNV dbSNP153 33..33 33 - - - 93826 RMVar_ID_93826 Human_SNP_ID_34583393 m1A Human chr1 + 155010054 155010053 155010055 GGAGGCAATGAGGGGACAGAACCAGGAGGCCAAGAGAGGGGCAAGAGTGAGGGCTGGATGATGGC GGAGGCAATGAGGGGACAGAACCAGGAGGCCA__AGAGGGGCAAGAGTGAGGGCTGGATGATGGC AAG A ZBTB7B Ensembl:ENSG00000160685 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:155009860..155010100 26863196 MeRIP-seq:(Medium) rs533403122 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3328605,Human_RBP_ID_8052761,Human_RBP_ID_8167190,Human_RBP_ID_18455187 93827 RMVar_ID_93827 Human_SNP_ID_34584321 m1A Human chr1 - 155013859 155013859 155013859 CGGGAAACACAGCTCCCAGCATCCCTCCCCCCACATCCTCCCCTCCCCCATGGGGCCAAGGAGCA CGGGAAACACAGCTCCCAGCATCCCTCCCCCCCCATCCTCCCCTCCCCCATGGGGCCAAGGAGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155013857..155014078 26863196 MeRIP-seq:(Medium) rs1275022937 Functional Loss SNV dbSNP153 33..33 33 - - - 93828 RMVar_ID_93828 Human_SNP_ID_34584539 m1A Human chr1 + 155014874 155014874 155014874 AGCTTTTCACTGAGGGCGGTGGCGGAGCTGTCATGGGGGCCGGGGGTAGCGGGACGGCCACTGGG AGCTTTTCACTGAGGGCGGTGGCGGAGCTGTCTTGGGGGCCGGGGGTAGCGGGACGGCCACTGGG A T ZBTB7B Ensembl:ENSG00000160685 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155014828..155015014 26863196 MeRIP-seq:(Medium) rs1483198158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851784,Human_RBP_ID_3934093,Human_RBP_ID_3996980,Human_RBP_ID_5234364,Human_RBP_ID_5519192,Human_RBP_ID_22023862,Human_RBP_ID_27388855 93829 RMVar_ID_93829 Human_SNP_ID_34584734 m1A Human chr1 - 155015444 155015444 155015444 GGGTTCGTAGCTCTGGGGACCCTCAGGAGGGGAGGCAGTTCCTGTGGGAGGGCTGTAGCTGTCCC GGGTTCGTAGCTCTGGGGACCCTCAGGAGGGGGGGCAGTTCCTGTGGGAGGGCTGTAGCTGTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155015397..155015652 26863196 MeRIP-seq:(Medium) rs200348493 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93830 RMVar_ID_93830 Human_SNP_ID_34585049 m1A Human chr1 - 155016435 155016435 155016435 GTGCATCGTCCTTGCGGCGCCGTCGGGTGCGCACCTCCAGGCAGTTCTGGCCTTTGAGGTGGCGC GTGCATCGTCCTTGCGGCGCCGTCGGGTGCGCGCCTCCAGGCAGTTCTGGCCTTTGAGGTGGCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155016384..155016518 26863196 MeRIP-seq:(Medium) rs774982140 Functional Loss SNV dbSNP153 33..33 33 - - - 93831 RMVar_ID_93831 Human_SNP_ID_34585086 m1A Human chr1 - 155016511 155016511 155016511 GTGTCCAGGTGGCCATTGGAGAGGTCGAGGCCAGCGGGGGATGCAGCAGCGGTAGAGGGTGGTGG GTGTCCAGGTGGCCATTGGAGAGGTCGAGGCCGGCGGGGGATGCAGCAGCGGTAGAGGGTGGTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155016476..155016550 26863196 MeRIP-seq:(Medium) rs761959889 Functional Loss SNV dbSNP153 33..33 33 - - - 93832 RMVar_ID_93832 Human_SNP_ID_34585290 m1A Human chr1 + 155017224 155017223 155017224 GGGTAGGTGGGGGAAAGCCAGGTGGAAGCTTGAAAGACTGGGGGACTGGGCCTGTAAGGAAGGAG GGGTAGGTGGGGGAAAGCCAGGTGGAAGCTTG_AAGACTGGGGGACTGGGCCTGTAAGGAAGGAG GA G ZBTB7B Ensembl:ENSG00000160685 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155017110..155017425 26863196 MeRIP-seq:(Medium) rs773017640 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9320194,Human_RBP_ID_26388644 Human_miRNA_ID_1460288 93833 RMVar_ID_93833 Human_SNP_ID_34589238 m1A Human chr1 - 155031165 155031165 155031165 ACCCTTCTTGCGCCAGACCATCGGCACCCGTGAGTGACCCCCTCCTGCCACATATGGTGCTCCCT ACCCTTCTTGCGCCAGACCATCGGCACCCGTGGGTGACCCCCTCCTGCCACATATGGTGCTCCCT T C DCST2 Ensembl:ENSG00000163354 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155031159..155031281 26863196 MeRIP-seq:(Medium) rs1226298715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_135696,Human_Splice_Rec_135726 93834 RMVar_ID_93834 Human_SNP_ID_34590211 m1A Human chr1 + 155034184 155034184 155034184 CTCCTCCTGGAACTCCTGCACACTATCCCCCAACTCGGTGTCCGCGCCTCCACCACCTCTCTGGT CTCCTCCTGGAACTCCTGCACACTATCCCCCACCTCGGTGTCCGCGCCTCCACCACCTCTCTGGT A C DCST1 Ensembl:ENSG00000163357 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155034144..155034276 26863196 MeRIP-seq:(Medium) rs895849818 Functional Loss SNV dbSNP153 33..33 33 - - - 93835 RMVar_ID_93835 Human_SNP_ID_34590243 m1A Human chr1 - 155034297 155034297 155034297 TGAAACAGTAGGAACTTAGGGGACCCTGGAGGAGGATGAGGGAGCCTGAGGAAGTGGTATGGGTG TGAAACAGTAGGAACTTAGGGGACCCTGGAGGTGGATGAGGGAGCCTGAGGAAGTGGTATGGGTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155034184..155034343 26863196 MeRIP-seq:(Medium) rs754697415 Functional Loss SNV dbSNP153 33..33 33 - - - 93836 RMVar_ID_93836 Human_SNP_ID_34595116 m1A Human chr1 + 155051351 155051351 155051351 GCCGCCGGCCGCTCCTCCGCGCGCTGTTCCGCACTTGCTGCCCTCGCCCGGCCCGGAGCGCCGCT GCCGCCGGCCGCTCCTCCGCGCGCTGTTCCGCGCTTGCTGCCCTCGCCCGGCCCGGAGCGCCGCT A G ADAM15 Ensembl:ENSG00000143537 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:155051301..155051494;chr1:155051301..155051562;chr1:155051301..155051634 26863196 MeRIP-seq:(Medium) rs1260195915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3997057,Human_RBP_ID_27388898 93837 RMVar_ID_93837 Human_SNP_ID_34595118 m1A Human chr1 - 155051354 155051354 155051354 GGCAGCGGCGCTCCGGGCCGGGCGAGGGCAGCAAGTGCGGAACAGCGCGCGGAGGAGCGGCCGGC GGCAGCGGCGCTCCGGGCCGGGCGAGGGCAGCGAGTGCGGAACAGCGCGCGGAGGAGCGGCCGGC T C DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155051301..155051443 26863196 MeRIP-seq:(Medium) rs993906289 Functional Loss SNV dbSNP153 33..33 33 - - - 93838 RMVar_ID_93838 Human_SNP_ID_34595136 m1A Human chr1 - 155051403 155051386 155051403 GGCTGCCCGCGCCCAGGAGCCCCAGGGCCCAGAGCAGCGCCAGCCGCATGGCAGCGGCGCTCCGG GGCTGCCCGCGCCCAGGAGCCCCAGGGCCCAG_________________GGCAGCGGCGCTCCGG CATGCGGCTGGCGCTGCT C DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:155051301..155051475 26863410 MeRIP-seq:(Medium) rs1374239807 Functional Loss DEL dbSNP153 33..49 33 - - - 93839 RMVar_ID_93839 Human_SNP_ID_34595144 m1A Human chr1 - 155051403 155051403 155051403 GGCTGCCCGCGCCCAGGAGCCCCAGGGCCCAGAGCAGCGCCAGCCGCATGGCAGCGGCGCTCCGG GGCTGCCCGCGCCCAGGAGCCCCAGGGCCCAGGGCAGCGCCAGCCGCATGGCAGCGGCGCTCCGG T C DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:155051301..155051475 26863410 MeRIP-seq:(Medium) rs757926512 Functional Loss SNV dbSNP153 33..33 33 - - - 93840 RMVar_ID_93840 Human_SNP_ID_34595339 m1A Human chr1 - 155052095 155052095 155052095 CACACAATGGCCCTCTCTCCTCCGGACACTCCACCCGCGCCTGCCCTCTCGGTCCCGGCCCAAGA CACACAATGGCCCTCTCTCCTCCGGACACTCCCCCCGCGCCTGCCCTCTCGGTCCCGGCCCAAGA T G DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155052088..155052495 26863196 MeRIP-seq:(Medium) rs1167317313 Functional Loss SNV dbSNP153 33..33 33 - - - 93841 RMVar_ID_93841 Human_SNP_ID_34595529 m1A Human chr1 - 155052721 155052721 155052721 TGGGAGATCGTCCTGAAGGACCTGGGGCTCCAAGGGCTCCCTCGGGGCCTTCTCTGACTCTGCCT TGGGAGATCGTCCTGAAGGACCTGGGGCTCCACGGGCTCCCTCGGGGCCTTCTCTGACTCTGCCT T G DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155052624..155052750 26863196 MeRIP-seq:(Medium) rs1385611371 Functional Loss SNV dbSNP153 33..33 33 - - - 93842 RMVar_ID_93842 Human_SNP_ID_34595997 m1A Human chr1 - 155054228 155054227 155054228 CTTTCTCTACTGTCATTAAATCCGCCCAGTATACCTGAGCCCAGAGCAGGTGCAGATGGACACCC CTTTCTCTACTGTCATTAAATCCGCCCAGTAT_CCTGAGCCCAGAGCAGGTGCAGATGGACACCC GT G DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:155054127..155054229 32194978 MeRIP-seq:(Medium) rs776504044 Functional Loss DEL dbSNP153 33..33 33 - - - 93843 RMVar_ID_93843 Human_SNP_ID_34598946 m1A Human chr1 - 155063831 155063831 155063831 CGGCCCAGAGGACAGTCCGCAGCAGGGGCAGCAGCCGCATCGCCCCCGAGGTCCGGTTTGGTCTG CGGCCCAGAGGACAGTCCGCAGCAGGGGCAGCGGCCGCATCGCCCCCGAGGTCCGGTTTGGTCTG T C DCST1-AS1,DCST1-AS1:2,DCST1-AS1:3 RNACentral:URS000075C771,RNACentral:URS0000D5A432,RNACentral:URS00008BC1C6 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155063780..155063918 26863196 MeRIP-seq:(Medium) rs938282528 Functional Loss SNV dbSNP153 33..33 33 - - - 93844 RMVar_ID_93844 Human_SNP_ID_34604191 m1A Human chr1 - 155085018 155085018 155085018 GAGCAAAGCCGCTTTCCATCTGACCGCTCCGCAGCCCCTCCCCAGGGTCCGCGTAGCCTTCCGAC GAGCAAAGCCGCTTTCCATCTGACCGCTCCGCGGCCCCTCCCCAGGGTCCGCGTAGCCTTCCGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155085014..155085120 26863196 MeRIP-seq:(Medium) rs978343240 Functional Loss SNV dbSNP153 33..33 33 - - - 93845 RMVar_ID_93845 Human_SNP_ID_34604765 m1A Human chr1 - 155086503 155086503 155086503 CCAAGAACGTCATGAGGAAGAAGGCGATGCCCACGGCCAGGGGCAGGTGTTCCCGTTTGGGGCTG CCAAGAACGTCATGAGGAAGAAGGCGATGCCCGCGGCCAGGGGCAGGTGTTCCCGTTTGGGGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155086461..155086560 26863196 MeRIP-seq:(Medium) rs759884576 Functional Loss SNV dbSNP153 33..33 33 - - - 93846 RMVar_ID_93846 Human_SNP_ID_34614939 m1A Human chr1 + 155127939 155127939 155127939 GGAGAAAGCCAGTGGGAACCCAGACCCATAGGAGACCCGCGTCCCCGCTCGGCCTGGCCAGGCCC GGAGAAAGCCAGTGGGAACCCAGACCCATAGGGGACCCGCGTCCCCGCTCGGCCTGGCCAGGCCC A G EFNA1 Ensembl:ENSG00000169242 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:155127876..155128075;chr1:155127876..155128151;chr1:155127876..155127950 26863196 MeRIP-seq:(Medium) rs766284771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745554,Human_RBP_ID_4073070,Human_RBP_ID_5519194,Human_RBP_ID_22428604 93847 RMVar_ID_93847 Human_SNP_ID_34615195 m1A Human chr1 - 155128757 155128757 155128757 AATTAACTCCTTCCTGCCCAGAACCTTCTGTAACCCCTTTAACCTCTTCTGTTCATTCTGAAGCT AATTAACTCCTTCCTGCCCAGAACCTTCTGTATCCCCTTTAACCTCTTCTGTTCATTCTGAAGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155128753..155128853 26863196 MeRIP-seq:(Medium) rs115018509 Functional Loss SNV dbSNP153 33..33 33 - - - 93848 RMVar_ID_93848 Human_SNP_ID_34615742 m1A Human chr1 + 155130506 155130504 155130506 GGAGGGGAGAGGGGGAGAGGAGGAGAGAGGGGAGAGAGGGGAGAGGGGAGAGGCTGTCTCAAGCT GGAGGGGAGAGGGGGAGAGGAGGAGAGAGGG__GAGAGGGGAGAGGGGAGAGGCTGTCTCAAGCT GGA G EFNA1 Ensembl:ENSG00000169242 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155130495..155130893 26863196 MeRIP-seq:(Medium) rs1173858813 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8167204,Human_RBP_ID_9410667,Human_RBP_ID_26774557 93849 RMVar_ID_93849 Human_SNP_ID_34615746 m1A Human chr1 + 155130506 155130506 155130506 GGAGGGGAGAGGGGGAGAGGAGGAGAGAGGGGAGAGAGGGGAGAGGGGAGAGGCTGTCTCAAGCT GGAGGGGAGAGGGGGAGAGGAGGAGAGAGGGGGGAGAGGGGAGAGGGGAGAGGCTGTCTCAAGCT A G EFNA1 Ensembl:ENSG00000169242 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155130495..155130893 26863196 MeRIP-seq:(Medium) rs1468950882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167204,Human_RBP_ID_9410667,Human_RBP_ID_26774557 93850 RMVar_ID_93850 Human_SNP_ID_34616477 m1A Human chr1 - 155133245 155133245 155133245 ACATTTCATCCTTCATTCCTCCGAGTCTGAATATGTTCCTCTTGCCTGGGCCACTTAATACTACT ACATTTCATCCTTCATTCCTCCGAGTCTGAATGTGTTCCTCTTGCCTGGGCCACTTAATACTACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155133225..155133486 26863196 MeRIP-seq:(Medium) rs767445135 Functional Loss SNV dbSNP153 33..33 33 - - - 93851 RMVar_ID_93851 Human_SNP_ID_34616623 m1A Human chr1 + 155133751 155133751 155133751 TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGACAATCCACAGGAGAAGAGACTTGCAGCAGGTG TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGTCAATCCACAGGAGAAGAGACTTGCAGCAGGTG A T EFNA1 Ensembl:ENSG00000169242 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4745 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_327815,Human_RBP_ID_851790,Human_RBP_ID_5536581,Human_RBP_ID_18969027,Human_RBP_ID_19035473,Human_RBP_ID_22634390,Human_RBP_ID_22751229,Human_RBP_ID_24556231,Human_RBP_ID_26774559 Human_Splice_Rec_136692,Human_Splice_Rec_136693,Human_Splice_Rec_136700,Human_Splice_Rec_136701,Human_Splice_Rec_136707,Human_Splice_Rec_136714,Human_Splice_Rec_136715,Human_Splice_Rec_136720,Human_Splice_Rec_136721 GWAS_ID_12205,GWAS_ID_12206,GWAS_ID_12207,GWAS_ID_12208,GWAS_ID_12209,GWAS_ID_12210,GWAS_ID_12211,GWAS_ID_12212,GWAS_ID_12213 RMVar_hsa_circ_59688 93852 RMVar_ID_93852 Human_SNP_ID_34617270 m1A Human chr1 - 155135902 155135902 155135902 TCCAGAAAGCCGCCCGCCTCCATTACGACTAGAGTCGGATCCCGCGCCCAGCGCCCGCCGCGAGC TCCAGAAAGCCGCCCGCCTCCATTACGACTAGTGTCGGATCCCGCGCCCAGCGCCCGCCGCGAGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155135851..155136317 26863196 MeRIP-seq:(Medium) rs770851521 Functional Loss SNV dbSNP153 33..33 33 - - - 93853 RMVar_ID_93853 Human_SNP_ID_34617302 m1A Human chr1 + 155135975 155135975 155135975 TTTACGGAGCATGCGTGGTCTTCACCCTTGGCATGTTCTCCGCCGGCCTGTGAGAGTGCGGCCGG TTTACGGAGCATGCGTGGTCTTCACCCTTGGCGTGTTCTCCGCCGGCCTGTGAGAGTGCGGCCGG A G SLC50A1 Ensembl:ENSG00000169241 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155135901..155136000 26863196 MeRIP-seq:(Medium) rs1332092502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327829,Human_RBP_ID_4074461,Human_RBP_ID_9320196,Human_RBP_ID_17338452 Human_Splice_Rec_136757,Human_Splice_Rec_136771,Human_Splice_Rec_136779,Human_Splice_Rec_136787,Human_Splice_Rec_136797,Human_Splice_Rec_136805,Human_Splice_Rec_136811,Human_Splice_Rec_136821 93854 RMVar_ID_93854 Human_SNP_ID_34618642 m1A Human chr1 - 155140492 155140492 155140492 GGGCCGCGCGGGGAAGGGGAGACGTGGGGTAGAGGTAAGTGTAGGTTGAAGGCTGAATGGGGAGG GGGCCGCGCGGGGAAGGGGAGACGTGGGGTAGTGGTAAGTGTAGGTTGAAGGCTGAATGGGGAGG T A DPM3 Ensembl:ENSG00000179085 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155139901..155140550 26863196 MeRIP-seq:(Medium) rs1019063610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073075,Human_RBP_ID_5109234 Human_Splice_Rec_136831,Human_Splice_Rec_136833 RMVar_hsa_circ_119499,RMVar_hsa_circ_136505 93855 RMVar_ID_93855 Human_SNP_ID_34625995 m1A Human chr1 - 155169525 155169525 155169525 CATCTTCTCCATGGTTGGTCTGTACTACATCAACAAGATCTCCTCCACCCTGTACCAGGCAGCAG CATCTTCTCCATGGTTGGTCTGTACTACATCAGCAAGATCTCCTCCACCCTGTACCAGGCAGCAG T C KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155169474..155169584 26863196 MeRIP-seq:(Medium) rs1229297585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22822,Human_RBP_ID_327879,Human_RBP_ID_1412681,Human_RBP_ID_1726360,Human_RBP_ID_2095489,Human_RBP_ID_3282332,Human_RBP_ID_5155719,Human_RBP_ID_8956449,Human_RBP_ID_9356930,Human_RBP_ID_10594463,Human_RBP_ID_17212751,Human_RBP_ID_17330579,Human_RBP_ID_17446523,Human_RBP_ID_17726751,Human_RBP_ID_18187280,Human_RBP_ID_19197293,Human_RBP_ID_22749473,Human_RBP_ID_22780326,Human_RBP_ID_24395516,Human_RBP_ID_24447596,Human_RBP_ID_26369266,Human_RBP_ID_26746767,Human_RBP_ID_26798957,Human_RBP_ID_27388924 Human_Splice_Rec_136842,Human_Splice_Rec_136848,Human_Splice_Rec_136856,Human_Splice_Rec_136864,Human_Splice_Rec_136872,Human_Splice_Rec_136878,Human_Splice_Rec_136882,Human_Splice_Rec_136888,Human_Splice_Rec_136894,Human_Splice_Rec_136902 Human_miRNA_ID_2368840,Human_miRNA_ID_2705117 RMVar_hsa_circ_95930,RMVar_hsa_circ_106282,RMVar_hsa_circ_106385,RMVar_hsa_circ_104135,RMVar_hsa_circ_136507,RMVar_hsa_circ_136508,RMVar_hsa_circ_136509,RMVar_hsa_circ_136506 93856 RMVar_ID_93856 Human_SNP_ID_34626002 m1A Human chr1 + 155169552 155169549 155169552 TCTTGTTGATGTAGTACAGACCAACCATGGAGAAGATGAAGCTATATGGTGAAGACAGAAAGGTC TCTTGTTGATGTAGTACAGACCAACCATGG___AGATGAAGCTATATGGTGAAGACAGAAAGGTC GAGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155169514..155169601 26863196 MeRIP-seq:(Medium) rs765212411 Functional Loss DEL dbSNP153 31..33 33 - - - 93857 RMVar_ID_93857 Human_SNP_ID_34626772 m1A Human chr1 + 155172601 155172601 155172601 AGGGAAGATCTTTGCTTGGAATCCTTTGCCAAAGACAAGATTCTCCAGATTATTGAAGGCCTGGT AGGGAAGATCTTTGCTTGGAATCCTTTGCCAAGGACAAGATTCTCCAGATTATTGAAGGCCTGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155172551..155172600 26863196 MeRIP-seq:(Medium) rs200430293 Functional Loss SNV dbSNP153 33..33 33 - - - 93858 RMVar_ID_93858 Human_SNP_ID_34626858 m1A Human chr1 - 155172824 155172824 155172824 TCCTGTCCCTGCTGCTCTTTGCTGGGATGCAGATGTACAGCCGTCAGCTGGCCTCCACCGAGTGG TCCTGTCCCTGCTGCTCTTTGCTGGGATGCAGTTGTACAGCCGTCAGCTGGCCTCCACCGAGTGG T A KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding exon,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:155172670..155172900 26863196 MeRIP-seq:(Medium) rs918862966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22824,Human_RBP_ID_327895,Human_RBP_ID_1412689,Human_RBP_ID_3997318,Human_RBP_ID_9319182,Human_RBP_ID_9359405,Human_RBP_ID_17647095,Human_RBP_ID_22429710,Human_RBP_ID_22560327,Human_RBP_ID_23334847 Human_Splice_Rec_136835,Human_Splice_Rec_136843,Human_Splice_Rec_136850,Human_Splice_Rec_136851,Human_Splice_Rec_136858,Human_Splice_Rec_136859,Human_Splice_Rec_136866,Human_Splice_Rec_136867,Human_Splice_Rec_136874,Human_Splice_Rec_136880,Human_Splice_Rec_136881,Human_Splice_Rec_136884,Human_Splice_Rec_136898 Human_miRNA_ID_2728692 RMVar_hsa_circ_95930,RMVar_hsa_circ_136509,RMVar_hsa_circ_46942,RMVar_hsa_circ_90082,RMVar_hsa_circ_136511 93859 RMVar_ID_93859 Human_SNP_ID_34626879 m1A Human chr1 - 155172884 155172884 155172884 CGTCCCTTCTCCCATCCCCTCCAGTGGTGGGTACGGGCACCTCGCTGGCGCTCTCCTCCCTCCTG CGTCCCTTCTCCCATCCCCTCCAGTGGTGGGTGCGGGCACCTCGCTGGCGCTCTCCTCCCTCCTG T C KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:155172551..155173300;chr1:155172580..155173276 26863196 MeRIP-seq:(Medium) rs1308037067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222855,Human_RBP_ID_4074467,Human_RBP_ID_5312693,Human_RBP_ID_5338496,Human_RBP_ID_9319182,Human_RBP_ID_17647095,Human_RBP_ID_22634393,Human_RBP_ID_24591889 Human_Splice_Rec_136850,Human_Splice_Rec_136858,Human_Splice_Rec_136866,Human_Splice_Rec_136874,Human_Splice_Rec_136880,Human_Splice_Rec_136884,Human_Splice_Rec_136898 Human_miRNA_ID_2442757 RMVar_hsa_circ_95930,RMVar_hsa_circ_136509,RMVar_hsa_circ_46942,RMVar_hsa_circ_90082,RMVar_hsa_circ_136511 93860 RMVar_ID_93860 Human_SNP_ID_34636225 m1A Human chr1 - 155206373 155206373 155206373 AATTGACCTGCTGACTGTGGGCGAGTCTCGGCAGATGGTAGCTGTGGCAGAGAAGATCCGGACAG AATTGACCTGCTGACTGTGGGCGAGTCTCGGCCGATGGTAGCTGTGGCAGAGAAGATCCGGACAG T G THBS3 Ensembl:ENSG00000169231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155206326..155206440 26863196 MeRIP-seq:(Medium) rs1407623219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10594606 Human_Splice_Rec_137424,Human_Splice_Rec_137468,Human_Splice_Rec_137510,Human_Splice_Rec_137550,Human_Splice_Rec_137596,Human_Splice_Rec_137630 RMVar_hsa_circ_17320,RMVar_hsa_circ_49762,RMVar_hsa_circ_107213,RMVar_hsa_circ_136519,RMVar_hsa_circ_368663 93861 RMVar_ID_93861 Human_SNP_ID_34637013 m1A Human chr1 - 155209046 155209046 155209046 CGCGGGCCTCGGGGGAGGGCGGCCGCCGGCCCATCCAGAGGTGGCCCACGTAGCGGGACAGCGCT CGCGGGCCTCGGGGGAGGGCGGCCGCCGGCCCGTCCAGAGGTGGCCCACGTAGCGGGACAGCGCT T C THBS3 Ensembl:ENSG00000169231 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155208999..155209143 26863196 MeRIP-seq:(Medium) rs772450682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107213,RMVar_hsa_circ_136519 93862 RMVar_ID_93862 Human_SNP_ID_34637037 m1A Human chr1 - 155209101 155209101 155209101 GGGGAGGCGAGGCTTCTTCTGGCCCGACTGGCAGCTGAACTGCGGGGGACTGGGCCGCGGGCCTC GGGGAGGCGAGGCTTCTTCTGGCCCGACTGGCCGCTGAACTGCGGGGGACTGGGCCGCGGGCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155208842..155209108 26863196 MeRIP-seq:(Medium) rs1379485040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107213,RMVar_hsa_circ_136519 93863 RMVar_ID_93863 Human_SNP_ID_34637170 m1A Human chr1 + 155209318 155209318 155209318 GGGGCTGGGGGCTGCCGTCAGTGGACCTGGACAGCCTGGCCGTGCTGGTGAGGGGTGGCGCCGGC GGGGCTGGGGGCTGCCGTCAGTGGACCTGGACGGCCTGGCCGTGCTGGTGAGGGGTGGCGCCGGC A G MTX1 Ensembl:ENSG00000173171 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:155209251..155209427 26863196 MeRIP-seq:(Medium) rs916979959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327912,Human_RBP_ID_4073078,Human_RBP_ID_18415075,Human_RBP_ID_19039333,Human_RBP_ID_22428611 Human_Splice_Rec_137673,Human_Splice_Rec_137687,Human_Splice_Rec_137699,Human_Splice_Rec_137713,Human_Splice_Rec_137727 93864 RMVar_ID_93864 Human_SNP_ID_34640722 m1A Human chr1 + 155221852 155221852 155221852 TTTAATAAGGACTAATGTTTATTGTGCCAAAGACAAAATTACAACAAATTTAACGATCTCGACTG TTTAATAAGGACTAATGTTTATTGTGCCAAAGGCAAAATTACAACAAATTTAACGATCTCGACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155221845..155221932 26863196 MeRIP-seq:(Medium) rs970996478 Functional Loss SNV dbSNP153 33..33 33 - - - 93865 RMVar_ID_93865 Human_SNP_ID_34644499 m1A Human chr1 - 155236443 155236443 155236443 TTGCAGGTACTGACAGACCCAGAAGCAGCTAAATATGTTCATGGCATTGCTGTACATTGGTACCT TTGCAGGTACTGACAGACCCAGAAGCAGCTAAGTATGTTCATGGCATTGCTGTACATTGGTACCT T C GBA Ensembl:ENSG00000177628 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:155236431..155237403 32194978 MeRIP-seq:(Medium) rs1064646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27169035 Human_Splice_Rec_137900,Human_Splice_Rec_137922,Human_Splice_Rec_137940,Human_Splice_Rec_137958,Human_Splice_Rec_137986,Human_Splice_Rec_137994 RMVar_hsa_circ_136529,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 93866 RMVar_ID_93866 Human_SNP_ID_34646648 m1A Human chr1 + 155244472 155244472 155244472 AGGTTAAGTGCGAACGCAGGGAGGGGACAGCTAAGATCCAAAGGTCGAAATATTCATTACGCCTA AGGTTAAGTGCGAACGCAGGGAGGGGACAGCTTAGATCCAAAGGTCGAAATATTCATTACGCCTA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:155244469..155244613 26863196 MeRIP-seq:(Medium) rs999958433 Functional Loss SNV dbSNP153 33..33 33 - - - 93867 RMVar_ID_93867 Human_SNP_ID_34647462 m1A Human chr1 - 155247643 155247643 155247643 TGTATACCCCCCAAAGTGTCCCTTTCCCTCCTACCTCTGGGGTCTCTTGCTGCTTGCCTCTGCTG TGTATACCCCCCAAAGTGTCCCTTTCCCTCCTGCCTCTGGGGTCTCTTGCTGCTTGCCTCTGCTG T C FAM189B Ensembl:ENSG00000160767 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155247594..155247782 26863196 MeRIP-seq:(Medium) rs1221091115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327947,Human_RBP_ID_4082305,Human_RBP_ID_5109719,Human_RBP_ID_17647704,Human_RBP_ID_18930043,Human_RBP_ID_19197595,Human_RBP_ID_27388948 Human_miRNA_ID_123,Human_miRNA_ID_3779,Human_miRNA_ID_7464,Human_miRNA_ID_11017,Human_miRNA_ID_14538,Human_miRNA_ID_18205,Human_miRNA_ID_21837,Human_miRNA_ID_25480,Human_miRNA_ID_490103,Human_miRNA_ID_493356,Human_miRNA_ID_1913210,Human_miRNA_ID_1915659,Human_miRNA_ID_1918108,Human_miRNA_ID_1920562,Human_miRNA_ID_1923020,Human_miRNA_ID_1925472,Human_miRNA_ID_1927924,Human_miRNA_ID_1930375,Human_miRNA_ID_2628200,Human_miRNA_ID_2641310,Human_miRNA_ID_3124055 RMVar_hsa_circ_124894,RMVar_hsa_circ_136533 93868 RMVar_ID_93868 Human_SNP_ID_34647690 m1A Human chr1 + 155248195 155248195 155248195 AGTGGGCAGGTGCAGGGCCCGAGGGCAGGGGAACTTTTTGGAAGGTGGGCACAGGGCGCCGTTTC AGTGGGCAGGTGCAGGGCCCGAGGGCAGGGGAGCTTTTTGGAAGGTGGGCACAGGGCGCCGTTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155248145..155248314 26863196 MeRIP-seq:(Medium) rs1217295650 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93869 RMVar_ID_93869 Human_SNP_ID_34649938 m1A Human chr1 + 155254732 155254732 155254732 TGGTGACGGAAGAGGCCACCATGCTGAAGGTGACCACCAGGATGCCCAGGAGCACTTGGACCAGC TGGTGACGGAAGAGGCCACCATGCTGAAGGTGCCCACCAGGATGCCCAGGAGCACTTGGACCAGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:155253609..155255384 32194978 MeRIP-seq:(Medium) rs1242810665 Functional Loss SNV dbSNP153 33..33 33 - - - 93870 RMVar_ID_93870 Human_SNP_ID_34650107 m1A Human chr1 - 155255194 155255194 155255194 GCTCCAGGCCGCCGCCCCCTCCTCACTCCTGGACCGGCCCTTCTCGGTGCCCCTCTTCCCTAGGG GCTCCAGGCCGCCGCCCCCTCCTCACTCCTGGGCCGGCCCTTCTCGGTGCCCCTCTTCCCTAGGG T C FAM189B Ensembl:ENSG00000160767 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:155255151..155255475 26863196 MeRIP-seq:(Medium) rs878436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328022,Human_RBP_ID_4076040,Human_RBP_ID_5413052,Human_RBP_ID_5432990,Human_RBP_ID_5456397,Human_RBP_ID_5484509,Human_RBP_ID_9319184,Human_RBP_ID_17072475,Human_RBP_ID_17647706,Human_RBP_ID_19197699 93871 RMVar_ID_93871 Human_SNP_ID_34650108 m1A Human chr1 - 155255194 155255194 155255194 GCTCCAGGCCGCCGCCCCCTCCTCACTCCTGGACCGGCCCTTCTCGGTGCCCCTCTTCCCTAGGG GCTCCAGGCCGCCGCCCCCTCCTCACTCCTGGCCCGGCCCTTCTCGGTGCCCCTCTTCCCTAGGG T G FAM189B Ensembl:ENSG00000160767 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:155255151..155255475 26863196 MeRIP-seq:(Medium) rs878436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328022,Human_RBP_ID_4076040,Human_RBP_ID_5413052,Human_RBP_ID_5432990,Human_RBP_ID_5456397,Human_RBP_ID_5484509,Human_RBP_ID_9319184,Human_RBP_ID_17072475,Human_RBP_ID_17647706,Human_RBP_ID_19197699 93872 RMVar_ID_93872 Human_SNP_ID_34650145 m1A Human chr1 + 155255345 155255345 155255345 GGCGCGGTCGGTGTGCCCTCAGGGCGTCCAGTAGGATCCGGGGCCGCCTGGTGGGGAGAGGCCGC GGCGCGGTCGGTGTGCCCTCAGGGCGTCCAGTGGGATCCGGGGCCGCCTGGTGGGGAGAGGCCGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155255129..155255417 26863196 MeRIP-seq:(Medium) rs1222217601 Functional Loss SNV dbSNP153 33..33 33 - - - 93873 RMVar_ID_93873 Human_SNP_ID_34650345 m1A Human chr1 + 155256151 155256150 155256152 ACACGCCTGTCAGGTTCAGCAGTCATGGCCATAGGATTGGGAGCACTACGGAGGAGCCATCAGTT ACACGCCTGTCAGGTTCAGCAGTCATGGCCAT__GATTGGGAGCACTACGGAGGAGCCATCAGTT TAG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:155256101..155256731 32194978 MeRIP-seq:(Medium) rs796401461 Functional Loss DEL dbSNP153 33..34 33 - - - 93874 RMVar_ID_93874 Human_SNP_ID_34650724 m1A Human chr1 - 155257374 155257374 155257374 CATTTTTTTCCTCTTTGTAGGAGTGACAGTTCATTCAATTTCTTCGTTTTCTTCTTCATTTTCTT CATTTTTTTCCTCTTTGTAGGAGTGACAGTTCGTTCAATTTCTTCGTTTTCTTCTTCATTTTCTT T C SCAMP3 Ensembl:ENSG00000116521 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:155257323..155258867 32194978 MeRIP-seq:(Medium) rs761338233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2095571,Human_RBP_ID_3282364,Human_RBP_ID_5694154,Human_RBP_ID_10594852,Human_RBP_ID_17212768,Human_RBP_ID_17330593,Human_RBP_ID_17446540 Human_Splice_Rec_138174,Human_Splice_Rec_138175,Human_Splice_Rec_138188,Human_Splice_Rec_138189,Human_Splice_Rec_138198,Human_Splice_Rec_138199,Human_Splice_Rec_138208,Human_Splice_Rec_138209,Human_Splice_Rec_138222,Human_Splice_Rec_138232 RMVar_hsa_circ_80200,RMVar_hsa_circ_109541,RMVar_hsa_circ_136539,RMVar_hsa_circ_91034,RMVar_hsa_circ_107759,RMVar_hsa_circ_79072,RMVar_hsa_circ_136540,RMVar_hsa_circ_136537,RMVar_hsa_circ_136538,RMVar_hsa_circ_111577,RMVar_hsa_circ_136542,RMVar_hsa_circ_136543 93875 RMVar_ID_93875 Human_SNP_ID_34651245 m1A Human chr1 - 155258950 155258950 155258950 GGTCCACCTGTTTTTTTGTGCCTTACAGCTCGACAGAACAATTGGCCCCCTCTACCTTCTTTTTG GGTCCACCTGTTTTTTTGTGCCTTACAGCTCGTCAGAACAATTGGCCCCCTCTACCTTCTTTTTG T A SCAMP3 Ensembl:ENSG00000116521 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155258901..155258975 26863196 MeRIP-seq:(Medium) rs1257477161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5157376,Human_RBP_ID_10594889,Human_RBP_ID_22637573 Human_Splice_Rec_138170,Human_Splice_Rec_138184,Human_Splice_Rec_138194,Human_Splice_Rec_138204,Human_Splice_Rec_138240 RMVar_hsa_circ_80200,RMVar_hsa_circ_109541,RMVar_hsa_circ_136539,RMVar_hsa_circ_91034,RMVar_hsa_circ_107759,RMVar_hsa_circ_136537,RMVar_hsa_circ_136538,RMVar_hsa_circ_111577,RMVar_hsa_circ_136542,RMVar_hsa_circ_136543 93876 RMVar_ID_93876 Human_SNP_ID_34651678 m1A Human chr1 - 155260388 155260388 155260388 CTGAAGAAACAGGAGGAGCTCAACCGGAAGGCAGAGGAGTTGGACCGAAGGGAGCGAGAGCTGCA CTGAAGAAACAGGAGGAGCTCAACCGGAAGGCGGAGGAGTTGGACCGAAGGGAGCGAGAGCTGCA T C SCAMP3 Ensembl:ENSG00000116521 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:155260340..155260491 32194978 MeRIP-seq:(Medium) rs768955194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221367,Human_RBP_ID_803466,Human_RBP_ID_857407,Human_RBP_ID_1412730,Human_RBP_ID_5694160,Human_RBP_ID_10594898,Human_RBP_ID_26314758 Human_Splice_Rec_138168,Human_Splice_Rec_138169,Human_Splice_Rec_138182,Human_Splice_Rec_138183,Human_Splice_Rec_138193,Human_Splice_Rec_138203,Human_Splice_Rec_138216,Human_Splice_Rec_138217,Human_Splice_Rec_138226,Human_Splice_Rec_138227,Human_Splice_Rec_138238,Human_Splice_Rec_138239 RMVar_hsa_circ_80200,RMVar_hsa_circ_91034,RMVar_hsa_circ_107759,RMVar_hsa_circ_136537,RMVar_hsa_circ_136538,RMVar_hsa_circ_111577,RMVar_hsa_circ_136542,RMVar_hsa_circ_82148,RMVar_hsa_circ_136543,RMVar_hsa_circ_136544 93877 RMVar_ID_93877 Human_SNP_ID_34651774 m1A Human chr1 - 155260657 155260657 155260657 AGATGATCACTAAGGTCTTTTCCTCAACAGCCACCACCAGCCTATGAGCCTCCAGCCCCTGCCCC AGATGATCACTAAGGTCTTTTCCTCAACAGCCGCCACCAGCCTATGAGCCTCCAGCCCCTGCCCC T C SCAMP3 Ensembl:ENSG00000116521 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155260551..155261257 26863196 MeRIP-seq:(Medium) rs771283991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18930053,Human_RBP_ID_26798972 Human_Splice_Rec_138166,Human_Splice_Rec_138180,Human_Splice_Rec_138214,Human_Splice_Rec_138224,Human_Splice_Rec_138236 Human_miRNA_ID_2050340 RMVar_hsa_circ_91034,RMVar_hsa_circ_107759,RMVar_hsa_circ_136537,RMVar_hsa_circ_136538 93878 RMVar_ID_93878 Human_SNP_ID_34651775 m1A Human chr1 - 155260657 155260657 155260657 AGATGATCACTAAGGTCTTTTCCTCAACAGCCACCACCAGCCTATGAGCCTCCAGCCCCTGCCCC AGATGATCACTAAGGTCTTTTCCTCAACAGCCCCCACCAGCCTATGAGCCTCCAGCCCCTGCCCC T G SCAMP3 Ensembl:ENSG00000116521 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155260551..155261257 26863196 MeRIP-seq:(Medium) rs771283991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18930053,Human_RBP_ID_26798972 Human_Splice_Rec_138166,Human_Splice_Rec_138180,Human_Splice_Rec_138214,Human_Splice_Rec_138224,Human_Splice_Rec_138236 Human_miRNA_ID_2050340 RMVar_hsa_circ_91034,RMVar_hsa_circ_107759,RMVar_hsa_circ_136537,RMVar_hsa_circ_136538 93879 RMVar_ID_93879 Human_SNP_ID_34652026 m1A Human chr1 - 155261653 155261653 155261653 ACGTCTACAACCCTTTTGAGACCCGGGAGGTGAGCTACTGGAGAGCATAGGAGTTCAAGGAAGGG ACGTCTACAACCCTTTTGAGACCCGGGAGGTGTGCTACTGGAGAGCATAGGAGTTCAAGGAAGGG T A SCAMP3 Ensembl:ENSG00000116521 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155261651..155261750 26863196 MeRIP-seq:(Medium) rs781458671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5694169 Human_Splice_Rec_138164,Human_Splice_Rec_138234,Human_Splice_Rec_138242 RMVar_hsa_circ_107759,RMVar_hsa_circ_136537 93880 RMVar_ID_93880 Human_SNP_ID_34652037 m1A Human chr1 + 155261672 155261672 155261672 GCTCTCCAGTAGCTCACCTCCCGGGTCTCAAAAGGGTTGTAGACGTCAAGCGTGGCATACTGCCG GCTCTCCAGTAGCTCACCTCCCGGGTCTCAAAGGGGTTGTAGACGTCAAGCGTGGCATACTGCCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155261651..155261750 26863196 MeRIP-seq:(Medium) rs146187850 Functional Loss SNV dbSNP153 33..33 33 - - - 93881 RMVar_ID_93881 Human_SNP_ID_34652045 m1A Human chr1 + 155261688 155261688 155261688 CCTCCCGGGTCTCAAAAGGGTTGTAGACGTCAAGCGTGGCATACTGCCGGCTGGGTCGGTGCTGG CCTCCCGGGTCTCAAAAGGGTTGTAGACGTCACGCGTGGCATACTGCCGGCTGGGTCGGTGCTGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155261676..155261700 26863196 MeRIP-seq:(Medium) rs760073 Functional Loss SNV dbSNP153 33..33 33 - - - 93882 RMVar_ID_93882 Human_SNP_ID_34652046 m1A Human chr1 + 155261688 155261688 155261688 CCTCCCGGGTCTCAAAAGGGTTGTAGACGTCAAGCGTGGCATACTGCCGGCTGGGTCGGTGCTGG CCTCCCGGGTCTCAAAAGGGTTGTAGACGTCAGGCGTGGCATACTGCCGGCTGGGTCGGTGCTGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155261676..155261700 26863196 MeRIP-seq:(Medium) rs760073 Functional Loss SNV dbSNP153 33..33 33 - - - 93883 RMVar_ID_93883 Human_SNP_ID_34652220 m1A Human chr1 - 155262212 155262207 155262213 GGCGAGTGAAGTGGACTCTGAGGGCTACCGCTACCGCCACTGCTGCGGCAGGGGCGTGGAGGGCA GGCGAGTGAAGTGGACTCTGAGGGCTACCGC______CACTGCTGCGGCAGGGGCGTGGAGGGCA GGCGGTA G SCAMP3 Ensembl:ENSG00000116521 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:155262076..155262228;chr1:155262056..155262329;chr1:155262041..155262277 26863196 MeRIP-seq:(Medium) rs1156451768 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_221369,Human_RBP_ID_741939,Human_RBP_ID_3997599,Human_RBP_ID_5137654,Human_RBP_ID_5234026,Human_RBP_ID_5311838,Human_RBP_ID_5484513,Human_RBP_ID_22428615 RMVar_hsa_circ_107759,RMVar_hsa_circ_136537 93884 RMVar_ID_93884 Human_SNP_ID_34652225 m1A Human chr1 + 155262226 155262224 155262226 CTGCCGCAGCAGTGGCGGTAGCGGTAGCCCTCAGAGTCCACTTCACTCGCCTCAGTTCGCCCCGC CTGCCGCAGCAGTGGCGGTAGCGGTAGCCCT__GAGTCCACTTCACTCGCCTCAGTTCGCCCCGC TCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155262041..155262300 26863196 MeRIP-seq:(Medium) rs575667038 Functional Loss DEL dbSNP153 32..33 33 - - - 93885 RMVar_ID_93885 Human_SNP_ID_34654104 m1A Human chr1 - 155268794 155268794 155268794 GCTTGCTCCGACCCCCCCTGCCCCCCGACAGCAGCACAGCAGCCGGAGAGCCAAGAGTGTAGAGG GCTTGCTCCGACCCCCCCTGCCCCCCGACAGCGGCACAGCAGCCGGAGAGCCAAGAGTGTAGAGG T C CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155268694..155269030;chr1:155268690..155269079;chr1:155268700..155268944 26863196 MeRIP-seq:(Medium) rs1305733956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23094,Human_RBP_ID_22560336,Human_RBP_ID_22847603,Human_RBP_ID_26843042 Human_Splice_Rec_138249,Human_Splice_Rec_138272,Human_Splice_Rec_138273,Human_Splice_Rec_138319,Human_Splice_Rec_138354,Human_Splice_Rec_138355 RMVar_hsa_circ_136546,RMVar_hsa_circ_108543,RMVar_hsa_circ_291123,RMVar_hsa_circ_113999,RMVar_hsa_circ_101046,RMVar_hsa_circ_136550,RMVar_hsa_circ_136551,RMVar_hsa_circ_88657,RMVar_hsa_circ_136553,RMVar_hsa_circ_98497,RMVar_hsa_circ_136554,RMVar_hsa_circ_136555 93886 RMVar_ID_93886 Human_SNP_ID_34654124 m1A Human chr1 - 155268816 155268815 155268816 CCGGCCCCCGCTCCGACACCTGGCTTGCTCCGACCCCCCCTGCCCCCCGACAGCAGCACAGCAGC CCGGCCCCCGCTCCGACACCTGGCTTGCTCCG_CCCCCCCTGCCCCCCGACAGCAGCACAGCAGC GT G CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155268680..155268975 26863196 MeRIP-seq:(Medium) rs869246115 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23094,Human_RBP_ID_10595149 RMVar_hsa_circ_136546,RMVar_hsa_circ_108543,RMVar_hsa_circ_291123,RMVar_hsa_circ_113999,RMVar_hsa_circ_101046,RMVar_hsa_circ_136550,RMVar_hsa_circ_136551,RMVar_hsa_circ_88657,RMVar_hsa_circ_136553,RMVar_hsa_circ_98497,RMVar_hsa_circ_136554,RMVar_hsa_circ_136555 93887 RMVar_ID_93887 Human_SNP_ID_34654132 m1A Human chr1 + 155268828 155268828 155268828 CTGTCGGGGGGCAGGGGGGGTCGGAGCAAGCCAGGTGTCGGAGCGGGGGCCGGAGGGAGGCGGGG CTGTCGGGGGGCAGGGGGGGTCGGAGCAAGCCCGGTGTCGGAGCGGGGGCCGGAGGGAGGCGGGG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:155268778..155268925 26863196 MeRIP-seq:(Medium) rs756581857 Functional Loss SNV dbSNP153 33..33 33 - - - 93888 RMVar_ID_93888 Human_SNP_ID_34654349 m1A Human chr1 - 155269555 155269555 155269555 ATATCAGCGGGAGAACAGCAGTTACCGCAGCCAGCGCAGCAGCCGGAGGAAGCACAGACGGCGGA ATATCAGCGGGAGAACAGCAGTTACCGCAGCCGGCGCAGCAGCCGGAGGAAGCACAGACGGCGGA T C CLK2 Ensembl:ENSG00000176444 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155269426..155269750 26863196 MeRIP-seq:(Medium) rs1471328129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9356938,Human_RBP_ID_22780399,Human_RBP_ID_26311898,Human_RBP_ID_26843057,Human_RBP_ID_27798592 Human_Splice_Rec_138247,Human_Splice_Rec_138271,Human_Splice_Rec_138295,Human_Splice_Rec_138317,Human_Splice_Rec_138353 Human_miRNA_ID_2330046,Human_miRNA_ID_2963123 RMVar_hsa_circ_136546,RMVar_hsa_circ_108543,RMVar_hsa_circ_291123,RMVar_hsa_circ_113999,RMVar_hsa_circ_101046,RMVar_hsa_circ_136550,RMVar_hsa_circ_136551,RMVar_hsa_circ_114454,RMVar_hsa_circ_88657,RMVar_hsa_circ_136553,RMVar_hsa_circ_98497,RMVar_hsa_circ_136554,RMVar_hsa_circ_136555,RMVar_hsa_circ_325211,RMVar_hsa_circ_136556 93889 RMVar_ID_93889 Human_SNP_ID_34654374 m1A Human chr1 + 155269602 155269602 155269602 CTGTTCTCCCGCTGATATTCATAGGAATGCCGATAGTCTGTGTCATAGTAGGCATCTCCCCGATC CTGTTCTCCCGCTGATATTCATAGGAATGCCGGTAGTCTGTGTCATAGTAGGCATCTCCCCGATC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:155269475..155269625 32194978 MeRIP-seq:(Medium) rs757895648 Functional Loss SNV dbSNP153 33..33 33 - - - 93890 RMVar_ID_93890 Human_SNP_ID_34655420 m1A Human chr1 + 155273441 155273441 155273441 GCTCGCACCGCCCCCGCCCGGGGCCCGATCCCAGCTCGGTCTCCGGCTCTGGCCTCTCCGCTCCG GCTCGCACCGCCCCCGCCCGGGGCCCGATCCCGGCTCGGTCTCCGGCTCTGGCCTCTCCGCTCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:155273226..155273485 26863196 MeRIP-seq:(Medium) rs961688114 Functional Loss SNV dbSNP153 33..33 33 - - - 93891 RMVar_ID_93891 Human_SNP_ID_34655421 m1A Human chr1 + 155273441 155273441 155273441 GCTCGCACCGCCCCCGCCCGGGGCCCGATCCCAGCTCGGTCTCCGGCTCTGGCCTCTCCGCTCCG GCTCGCACCGCCCCCGCCCGGGGCCCGATCCCTGCTCGGTCTCCGGCTCTGGCCTCTCCGCTCCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:155273226..155273485 26863196 MeRIP-seq:(Medium) rs961688114 Functional Loss SNV dbSNP153 33..33 33 - - - 93892 RMVar_ID_93892 Human_SNP_ID_34656563 m1A Human chr1 - 155277572 155277572 155277572 TGCTCTGCCTCCATGGCGCCCACCCCGCTTACACGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC TGCTCTGCCTCCATGGCGCCCACCCCGCTTACTCGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC T A CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155277481..155277692;chr1:155277470..155277693 26863196 MeRIP-seq:(Medium) rs1369618157 Functional Loss SNV dbSNP153 33..33 33 - - - 93893 RMVar_ID_93893 Human_SNP_ID_34656564 m1A Human chr1 - 155277572 155277572 155277572 TGCTCTGCCTCCATGGCGCCCACCCCGCTTACACGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC TGCTCTGCCTCCATGGCGCCCACCCCGCTTACGCGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC T C CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155277481..155277692;chr1:155277470..155277693 26863196 MeRIP-seq:(Medium) rs1369618157 Functional Loss SNV dbSNP153 33..33 33 - - - 93894 RMVar_ID_93894 Human_SNP_ID_34656565 m1A Human chr1 - 155277572 155277572 155277572 TGCTCTGCCTCCATGGCGCCCACCCCGCTTACACGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC TGCTCTGCCTCCATGGCGCCCACCCCGCTTACCCGCTCGGCCTCCTAGAGCCCTCTGTGGCCATC T G CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155277481..155277692;chr1:155277470..155277693 26863196 MeRIP-seq:(Medium) rs1369618157 Functional Loss SNV dbSNP153 33..33 33 - - - 93895 RMVar_ID_93895 Human_SNP_ID_34658407 m1A Human chr1 + 155284276 155284276 155284276 AATAGGAGCGAGGAGGTGGGGAGGAGGGAGGAAAGGGGAAGGAGACCCAGAAGAAGTGCTCGTGT AATAGGAGCGAGGAGGTGGGGAGGAGGGAGGAGAGGGGAAGGAGACCCAGAAGAAGTGCTCGTGT A G HCN3 Ensembl:ENSG00000143630 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155284227..155284440 26863196 MeRIP-seq:(Medium) rs116597799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25185,Human_RBP_ID_9412030,Human_RBP_ID_18928662,Human_RBP_ID_22560340 93896 RMVar_ID_93896 Human_SNP_ID_34666052 m1A Human chr1 - 155310190 155310190 155310190 AGTCATGAATCCCTCACCTCCTTGAGCCGGGCAATAGCATCTCCTATCTCTGGGTGCCCCATCTC AGTCATGAATCCCTCACCTCCTTGAGCCGGGCGATAGCATCTCCTATCTCTGGGTGCCCCATCTC T C lnc-PKLR-1,lnc-PKLR-1:2 RNACentral:URS00009AF9AA,RNACentral:URS00008BD07B lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155310021..155310262 26863196 MeRIP-seq:(Medium) rs1459110829 Functional Loss SNV dbSNP153 33..33 33 - - - 93897 RMVar_ID_93897 Human_SNP_ID_34666539 m1A Human chr1 + 155312335 155312335 155312335 GTGGTAGTAGCATTCCGGGAGCTGGTGGAGCCAAGGAAACAGGATGCTGATAGTCTCCAGCGGGC GTGGTAGTAGCATTCCGGGAGCTGGTGGAGCCGAGGAAACAGGATGCTGATAGTCTCCAGCGGGC A G FDPS Ensembl:ENSG00000160752 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155312212..155312450 26863196 MeRIP-seq:(Medium) rs993376440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743734,Human_RBP_ID_3936743,Human_RBP_ID_4076047,Human_RBP_ID_8286581,Human_RBP_ID_9359425,Human_RBP_ID_18543932,Human_RBP_ID_22707149,Human_RBP_ID_22870959,Human_RBP_ID_24528789,Human_RBP_ID_26773157 Human_Splice_Rec_138448,Human_Splice_Rec_138449,Human_Splice_Rec_138466,Human_Splice_Rec_138467,Human_Splice_Rec_138480,Human_Splice_Rec_138481,Human_Splice_Rec_138498,Human_Splice_Rec_138499,Human_Splice_Rec_138508,Human_Splice_Rec_138509,Human_Splice_Rec_138528,Human_Splice_Rec_138529,Human_Splice_Rec_138534,Human_Splice_Rec_138535,Human_Splice_Rec_138542,Human_Splice_Rec_138543,Human_Splice_Rec_138560,Human_Splice_Rec_138561,Human_Splice_Rec_138566,Human_Splice_Rec_138572,Human_Splice_Rec_138573,Human_Splice_Rec_138586,Human_Splice_Rec_138587,Human_Splice_Rec_138606,Human_Splice_Rec_138607,Human_Splice_Rec_138612,Human_Splice_Rec_138613,Human_Splice_Rec_138622,Human_Splice_Rec_138623,Human_Splice_Rec_138640,Human_Splice_Rec_138641,Human_Splice_Rec_138648,Human_Splice_Rec_138649 Human_miRNA_ID_2216713,Human_miRNA_ID_2216714 RMVar_hsa_circ_101793,RMVar_hsa_circ_115755,RMVar_hsa_circ_99858,RMVar_hsa_circ_136560,RMVar_hsa_circ_136562,RMVar_hsa_circ_105685,RMVar_hsa_circ_136561,RMVar_hsa_circ_49079,RMVar_hsa_circ_136563 93898 RMVar_ID_93898 Human_SNP_ID_34666546 m1A Human chr1 + 155312361 155312361 155312361 GGAGCCAAGGAAACAGGATGCTGATAGTCTCCAGCGGGCCTGGACTGTGGGCTGGTGTGTGGAAC GGAGCCAAGGAAACAGGATGCTGATAGTCTCCCGCGGGCCTGGACTGTGGGCTGGTGTGTGGAAC A C FDPS Ensembl:ENSG00000160752 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155312313..155312573 26863196 MeRIP-seq:(Medium) rs370107498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22131,Human_RBP_ID_328101,Human_RBP_ID_1074426,Human_RBP_ID_1412822,Human_RBP_ID_3997712,Human_RBP_ID_5694287,Human_RBP_ID_8286582,Human_RBP_ID_10595400,Human_RBP_ID_18543932,Human_RBP_ID_22429713,Human_RBP_ID_23335026,Human_RBP_ID_24528789,Human_RBP_ID_26311902,Human_RBP_ID_26773157,Human_RBP_ID_26843116 Human_Splice_Rec_138449,Human_Splice_Rec_138467,Human_Splice_Rec_138481,Human_Splice_Rec_138499,Human_Splice_Rec_138509,Human_Splice_Rec_138529,Human_Splice_Rec_138535,Human_Splice_Rec_138543,Human_Splice_Rec_138561,Human_Splice_Rec_138573,Human_Splice_Rec_138587,Human_Splice_Rec_138607,Human_Splice_Rec_138613,Human_Splice_Rec_138623,Human_Splice_Rec_138641,Human_Splice_Rec_138649 Human_miRNA_ID_2656059,Human_miRNA_ID_2656060 RMVar_hsa_circ_101793,RMVar_hsa_circ_115755,RMVar_hsa_circ_99858,RMVar_hsa_circ_136560,RMVar_hsa_circ_136562,RMVar_hsa_circ_105685,RMVar_hsa_circ_136561,RMVar_hsa_circ_49079,RMVar_hsa_circ_136563 93899 RMVar_ID_93899 Human_SNP_ID_34666810 m1A Human chr1 + 155313374 155313374 155313374 TTTCATTAGTGGCAGGGGGACTGGGTTCTGGGAGGGGTGCCATGCCCGAGGAGGGTGGCAGTGAG TTTCATTAGTGGCAGGGGGACTGGGTTCTGGGGGGGGTGCCATGCCCGAGGAGGGTGGCAGTGAG A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155313351..155313800 26863196 MeRIP-seq:(Medium) rs918067132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222637,Human_RBP_ID_743738,Human_RBP_ID_802499,Human_RBP_ID_5694299,Human_RBP_ID_8052775,Human_RBP_ID_22870960 RMVar_hsa_circ_101793,RMVar_hsa_circ_99858,RMVar_hsa_circ_136560,RMVar_hsa_circ_136562,RMVar_hsa_circ_105685,RMVar_hsa_circ_49079,RMVar_hsa_circ_136563 93900 RMVar_ID_93900 Human_SNP_ID_34667922 m1A Human chr1 - 155318180 155318180 155318180 TCCAGGAGGTTAGCATCATTGATGGCATCCAAACCCACGCCCGGCTGTCATGACAGACAGAAAAA TCCAGGAGGTTAGCATCATTGATGGCATCCAATCCCACGCCCGGCTGTCATGACAGACAGAAAAA T A RUSC1-AS1 Ensembl:ENSG00000225855 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155318166..155318267 26863196 MeRIP-seq:(Medium) rs779023160 Functional Loss SNV dbSNP153 33..33 33 - - - 93901 RMVar_ID_93901 Human_SNP_ID_34668489 m1A Human chr1 + 155320459 155320459 155320459 GAGGCTGAGAAAGTGGCCCGGGTGAAGGCGCTATATGAGGAGCTGGATCTGCCAGCAGTGTTCTT GAGGCTGAGAAAGTGGCCCGGGTGAAGGCGCTGTATGAGGAGCTGGATCTGCCAGCAGTGTTCTT A G FDPS Ensembl:ENSG00000160752 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155320242..155320609 26863196 MeRIP-seq:(Medium) rs760412972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328111,Human_RBP_ID_971588,Human_RBP_ID_1726439,Human_RBP_ID_4082422,Human_RBP_ID_5694332,Human_RBP_ID_8755151,Human_RBP_ID_9356941,Human_RBP_ID_17646164,Human_RBP_ID_17764121,Human_RBP_ID_19198082,Human_RBP_ID_22429717,Human_RBP_ID_22750297,Human_RBP_ID_22847733,Human_RBP_ID_27169124,Human_RBP_ID_27800868 Human_Splice_Rec_138462,Human_Splice_Rec_138494,Human_Splice_Rec_138522,Human_Splice_Rec_138556,Human_Splice_Rec_138600,Human_Splice_Rec_138636,Human_Splice_Rec_138672,Human_Splice_Rec_138678,Human_Splice_Rec_138680 93902 RMVar_ID_93902 Human_SNP_ID_34668569 m1A Human chr1 + 155320653 155320650 155320654 CAAGGGCGGGGAGAGGAGGCTCTCAATAAATAATCGTGTAACCTTCTTGTGGTTCTGTTCTTGCT CAAGGGCGGGGAGAGGAGGCTCTCAATAAA____CGTGTAACCTTCTTGTGGTTCTGTTCTTGCT ATAAT A FDPS Ensembl:ENSG00000160752 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155320651..155320675 26863196 MeRIP-seq:(Medium) rs1266166601 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_328119,Human_RBP_ID_971589,Human_RBP_ID_2095654,Human_RBP_ID_5484517,Human_RBP_ID_5694333,Human_RBP_ID_17764905,Human_RBP_ID_18552622,Human_RBP_ID_22369422,Human_RBP_ID_22426011,Human_RBP_ID_26578461 93903 RMVar_ID_93903 Human_SNP_ID_34670134 m1A Human chr1 - 155324546 155324546 155324546 CCCGGAACTCCGGGAGCGGGATGGCCGCGCTCACCTCCCGCCTGCCCTGCTAGGGCCTGTAGGGC CCCGGAACTCCGGGAGCGGGATGGCCGCGCTCGCCTCCCGCCTGCCCTGCTAGGGCCTGTAGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155324526..155324702 26863196 MeRIP-seq:(Medium) rs778106605 Functional Loss SNV dbSNP153 33..33 33 - - - 93904 RMVar_ID_93904 Human_SNP_ID_34670217 m1A Human chr1 - 155324807 155324807 155324807 GTAAGGGAAGAAGGGCGCGGTAACACTTACCAAGTGTTATTCCGAGGACTCCGGGCTCCCGCACA GTAAGGGAAGAAGGGCGCGGTAACACTTACCAGGTGTTATTCCGAGGACTCCGGGCTCCCGCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155324802..155324928 26863196 MeRIP-seq:(Medium) rs766316152 Functional Loss SNV dbSNP153 33..33 33 - - - 93905 RMVar_ID_93905 Human_SNP_ID_34670879 m1A Human chr1 - 155326693 155326693 155326693 GTGGTGGTGCTCAAAGAGCAGGTCCAGGTGGAAAGTGAGCACCGACAATGGCTGCAGCAGGAGCA GTGGTGGTGCTCAAAGAGCAGGTCCAGGTGGACAGTGAGCACCGACAATGGCTGCAGCAGGAGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155326651..155326815 26863196 MeRIP-seq:(Medium) rs1232988101 Functional Loss SNV dbSNP153 33..33 33 - - - 93906 RMVar_ID_93906 Human_SNP_ID_34671948 m1A Human chr1 - 155330625 155330625 155330625 GGAAAATGCTTCTGGGATGGTGTTCACTGGCCATTCCATTCCCAGGTGACAGGAAGGAGACACAT GGAAAATGCTTCTGGGATGGTGTTCACTGGCCTTTCCATTCCCAGGTGACAGGAAGGAGACACAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155330576..155330650 26863196 MeRIP-seq:(Medium) rs941239211 Functional Loss SNV dbSNP153 33..33 33 - - - 93907 RMVar_ID_93907 Human_SNP_ID_34671949 m1A Human chr1 - 155330625 155330625 155330625 GGAAAATGCTTCTGGGATGGTGTTCACTGGCCATTCCATTCCCAGGTGACAGGAAGGAGACACAT GGAAAATGCTTCTGGGATGGTGTTCACTGGCCGTTCCATTCCCAGGTGACAGGAAGGAGACACAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:155330576..155330650 26863196 MeRIP-seq:(Medium) rs941239211 Functional Loss SNV dbSNP153 33..33 33 - - - 93908 RMVar_ID_93908 Human_SNP_ID_34678963 m1A Human chr1 - 155357365 155357365 155357365 CTGAGGAACCCAGTGAAAATATCAACACCCCAACTAGATTGACCCCCCAATTACAGATGAAGCCA CTGAGGAACCCAGTGAAAATATCAACACCCCAGCTAGATTGACCCCCCAATTACAGATGAAGCCA T C ASH1L Ensembl:ENSG00000116539 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155357277..155357441 26863196 MeRIP-seq:(Medium) rs887197165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18170,Human_RBP_ID_8043674,Human_RBP_ID_17726880 Human_Splice_Rec_138924,Human_Splice_Rec_138925,Human_Splice_Rec_138976,Human_Splice_Rec_138977 RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,RMVar_hsa_circ_362764,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_353828,RMVar_hsa_circ_100989,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_126702,RMVar_hsa_circ_91291,RMVar_hsa_circ_136576,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136581,RMVar_hsa_circ_136580,RMVar_hsa_circ_116685,RMVar_hsa_circ_125118,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136587,RMVar_hsa_circ_136588,RMVar_hsa_circ_136586,RMVar_hsa_circ_107116,RMVar_hsa_circ_104606,RMVar_hsa_circ_136591,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_71110,RMVar_hsa_circ_313297,RMVar_hsa_circ_136595,RMVar_hsa_circ_64146,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_337790,RMVar_hsa_circ_136600,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_349043,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,RMVar_hsa_circ_136604,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_136605,RMVar_hsa_circ_357101,RMVar_hsa_circ_360143,RMVar_hsa_circ_266780,RMVar_hsa_circ_288993,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_136609,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608 93909 RMVar_ID_93909 Human_SNP_ID_34678964 m1A Human chr1 - 155357365 155357365 155357365 CTGAGGAACCCAGTGAAAATATCAACACCCCAACTAGATTGACCCCCCAATTACAGATGAAGCCA CTGAGGAACCCAGTGAAAATATCAACACCCCACCTAGATTGACCCCCCAATTACAGATGAAGCCA T G ASH1L Ensembl:ENSG00000116539 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155357277..155357441 26863196 MeRIP-seq:(Medium) rs887197165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18170,Human_RBP_ID_8043674,Human_RBP_ID_17726880 Human_Splice_Rec_138924,Human_Splice_Rec_138925,Human_Splice_Rec_138976,Human_Splice_Rec_138977 RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,RMVar_hsa_circ_362764,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_353828,RMVar_hsa_circ_100989,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_126702,RMVar_hsa_circ_91291,RMVar_hsa_circ_136576,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136581,RMVar_hsa_circ_136580,RMVar_hsa_circ_116685,RMVar_hsa_circ_125118,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136587,RMVar_hsa_circ_136588,RMVar_hsa_circ_136586,RMVar_hsa_circ_107116,RMVar_hsa_circ_104606,RMVar_hsa_circ_136591,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_71110,RMVar_hsa_circ_313297,RMVar_hsa_circ_136595,RMVar_hsa_circ_64146,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_337790,RMVar_hsa_circ_136600,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_349043,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,RMVar_hsa_circ_136604,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_136605,RMVar_hsa_circ_357101,RMVar_hsa_circ_360143,RMVar_hsa_circ_266780,RMVar_hsa_circ_288993,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_136609,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608 93910 RMVar_ID_93910 Human_SNP_ID_34704184 m1A Human chr1 - 155458759 155458759 155458759 TAAATAAAAAAGCCAGTGTGGTCAGACTAAAGACGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT TAAATAAAAAAGCCAGTGTGGTCAGACTAAAGTCGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGT T A ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155458745..155458838 26863196 MeRIP-seq:(Medium) rs145052357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1149835 RMVar_hsa_circ_366827,RMVar_hsa_circ_69363,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_55595,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_136594,RMVar_hsa_circ_85679,RMVar_hsa_circ_136606,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_96092,RMVar_hsa_circ_136618,RMVar_hsa_circ_358840,RMVar_hsa_circ_136620,RMVar_hsa_circ_53527,RMVar_hsa_circ_136624,RMVar_hsa_circ_270411,RMVar_hsa_circ_136628,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_277790,RMVar_hsa_circ_136632,RMVar_hsa_circ_277338,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136634,RMVar_hsa_circ_136635,RMVar_hsa_circ_136633 93911 RMVar_ID_93911 Human_SNP_ID_34744570 m1A Human chr1 - 155612521 155612521 155612521 GGAAGCTGACAGGTGGCTCGGGTCGCAGGCCCAGGCTCCCACCCAAGGACAAGGGGCAGACAAGA GGAAGCTGACAGGTGGCTCGGGTCGCAGGCCCTGGCTCCCACCCAAGGACAAGGGGCAGACAAGA T A lnc-YY1AP1-3 RNACentral:URS00008C3E43 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155612471..155612554 26863196 MeRIP-seq:(Medium) rs1207609536 Functional Loss SNV dbSNP153 33..33 33 - - - 93912 RMVar_ID_93912 Human_SNP_ID_34753830 m1A Human chr1 + 155648467 155648467 155648467 GGAGCAGTCTCAGGTGAGGCAAAAGTAGAAGGAGGCTTCTCAGCAGAGTCTCCAACTGCTTCATC GGAGCAGTCTCAGGTGAGGCAAAAGTAGAAGGCGGCTTCTCAGCAGAGTCTCCAACTGCTTCATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155648465..155648584 26863196 MeRIP-seq:(Medium) rs1470125636 Functional Loss SNV dbSNP153 33..33 33 - - - 93913 RMVar_ID_93913 Human_SNP_ID_34756585 m1A Human chr1 - 155659861 155659861 155659861 CCCAAAGTGGAACATAGCCCAGGGCCTCCACCAGTCGATAAACAGTGCCAAGAAGGATTGTCAGA CCCAAAGTGGAACATAGCCCAGGGCCTCCACCTGTCGATAAACAGTGCCAAGAAGGATTGTCAGA T A YY1AP1,AL353807.3 Ensembl:ENSG00000163374,Ensembl:ENSG00000246203 Protein coding,Pseudogene CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155659810..155659908 26863196 MeRIP-seq:(Medium) rs1558294477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438618,Human_RBP_ID_1726613,Human_RBP_ID_5092260,Human_RBP_ID_8171301,Human_RBP_ID_8286771,Human_RBP_ID_8755868,Human_RBP_ID_9552717,Human_RBP_ID_10481936,Human_RBP_ID_10599435,Human_RBP_ID_17182651,Human_RBP_ID_17204388,Human_RBP_ID_18158661,Human_RBP_ID_18552803,Human_RBP_ID_27169261,Human_RBP_ID_27389116 Human_miRNA_ID_137713,Human_miRNA_ID_414385,Human_miRNA_ID_1821262,Human_miRNA_ID_1876110,Human_miRNA_ID_1877796,Human_miRNA_ID_1910824,Human_miRNA_ID_1912636 93914 RMVar_ID_93914 Human_SNP_ID_34761453 m1A Human chr1 + 155676597 155676597 155676597 GGAGTCTCTTCCTTTGTGCTGGGTCCAGAATCAGGGTCTGATGAACTTCCTTACACTGGGGTTTA GGAGTCTCTTCCTTTGTGCTGGGTCCAGAATCGGGGTCTGATGAACTTCCTTACACTGGGGTTTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155676504..155676680 26863196 MeRIP-seq:(Medium) rs1474626005 Functional Loss SNV dbSNP153 33..33 33 - - - 93915 RMVar_ID_93915 Human_SNP_ID_34764556 m1A Human chr1 + 155688408 155688408 155688408 CTAAGGGCGCCTAGCGACACCCCCAACCTCCCACTCCTCCCTCCTCGCGTTCTTCCCCACGGTCC CTAAGGGCGCCTAGCGACACCCCCAACCTCCCTCTCCTCCCTCCTCGCGTTCTTCCCCACGGTCC A T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:155688401..155688700 26863196 MeRIP-seq:(Medium) rs955953653 Functional Loss SNV dbSNP153 33..33 33 - - - 93916 RMVar_ID_93916 Human_SNP_ID_34764653 m1A Human chr1 + 155688643 155688643 155688643 CCCCTCAGACCCTGTCAAGCCGGCTCCAGCGCAGGCCCTCACGCGTACCTTCAGCGGCGCGAGCC CCCCTCAGACCCTGTCAAGCCGGCTCCAGCGCGGGCCCTCACGCGTACCTTCAGCGGCGCGAGCC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:155688484..155688652 26863196 MeRIP-seq:(Medium) rs1278163603 Functional Loss SNV dbSNP153 33..33 33 - - - 93917 RMVar_ID_93917 Human_SNP_ID_34770460 m1A Human chr1 - 155709754 155709752 155709755 GCATCATCCTTGCACTGTTACAAAAAAAAAAAAAGTGAAAAGGTAAACCACAAATGGGAAAAGAT GCATCATCCTTGCACTGTTACAAAAAAAAAA___GTGAAAAGGTAAACCACAAATGGGAAAAGAT CTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155709751..155709800 26863196 MeRIP-seq:(Medium) rs372695062 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 93918 RMVar_ID_93918 Human_SNP_ID_34770461 m1A Human chr1 - 155709754 155709752 155709755 GCATCATCCTTGCACTGTTACAAAAAAAAAAAAAGTGAAAAGGTAAACCACAAATGGGAAAAGAT GCATCATCCTTGCACTGTTACAAAAAAAAAA__AGTGAAAAGGTAAACCACAAATGGGAAAAGAT CTTT CT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155709751..155709800 26863196 MeRIP-seq:(Medium) rs372695062 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 93919 RMVar_ID_93919 Human_SNP_ID_34770466 m1A Human chr1 - 155709754 155709754 155709754 GCATCATCCTTGCACTGTTACAAAAAAAAAAAAAGTGAAAAGGTAAACCACAAATGGGAAAAGAT GCATCATCCTTGCACTGTTACAAAAAAAAAAACAGTGAAAAGGTAAACCACAAATGGGAAAAGAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155709751..155709800 26863196 MeRIP-seq:(Medium) rs554664018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 93920 RMVar_ID_93920 Human_SNP_ID_34773343 m1A Human chr1 + 155721566 155721566 155721566 GCACGAGGGTCAGCACTACAACATCTCCCCCCAGGATTTGGAGACTGTATTTCCCCATGGCCTTC GCACGAGGGTCAGCACTACAACATCTCCCCCCGGGATTTGGAGACTGTATTTCCCCATGGCCTTC A G DAP3 Ensembl:ENSG00000132676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:155721470..155721665;chr1:155721456..155721695 26863196 MeRIP-seq:(Medium) rs1465445158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328281,Human_RBP_ID_10600921,Human_RBP_ID_17727012,Human_RBP_ID_18552839,Human_RBP_ID_27389134 Human_Splice_Rec_139706,Human_Splice_Rec_139707,Human_Splice_Rec_139734,Human_Splice_Rec_139735,Human_Splice_Rec_139754,Human_Splice_Rec_139755,Human_Splice_Rec_139778,Human_Splice_Rec_139779,Human_Splice_Rec_139808,Human_Splice_Rec_139809,Human_Splice_Rec_139832,Human_Splice_Rec_139833,Human_Splice_Rec_139856,Human_Splice_Rec_139862,Human_Splice_Rec_139863,Human_Splice_Rec_139872,Human_Splice_Rec_139873,Human_Splice_Rec_139884,Human_Splice_Rec_139885,Human_Splice_Rec_139896,Human_Splice_Rec_139897,Human_Splice_Rec_139912,Human_Splice_Rec_139913,Human_Splice_Rec_139918,Human_Splice_Rec_139919 Human_miRNA_ID_2038452,Human_miRNA_ID_2787745,Human_miRNA_ID_2817354,Human_miRNA_ID_3017434 RMVar_hsa_circ_25131,RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_280673,RMVar_hsa_circ_301144,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136672,RMVar_hsa_circ_136673,RMVar_hsa_circ_325523,RMVar_hsa_circ_276721,RMVar_hsa_circ_136677,RMVar_hsa_circ_136674,RMVar_hsa_circ_136675,RMVar_hsa_circ_271004,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_118932,RMVar_hsa_circ_136676 93921 RMVar_ID_93921 Human_SNP_ID_34773344 m1A Human chr1 + 155721566 155721566 155721566 GCACGAGGGTCAGCACTACAACATCTCCCCCCAGGATTTGGAGACTGTATTTCCCCATGGCCTTC GCACGAGGGTCAGCACTACAACATCTCCCCCCTGGATTTGGAGACTGTATTTCCCCATGGCCTTC A T DAP3 Ensembl:ENSG00000132676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:155721470..155721665;chr1:155721456..155721695 26863196 MeRIP-seq:(Medium) rs1465445158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328281,Human_RBP_ID_10600921,Human_RBP_ID_17727012,Human_RBP_ID_18552839,Human_RBP_ID_27389134 Human_Splice_Rec_139706,Human_Splice_Rec_139707,Human_Splice_Rec_139734,Human_Splice_Rec_139735,Human_Splice_Rec_139754,Human_Splice_Rec_139755,Human_Splice_Rec_139778,Human_Splice_Rec_139779,Human_Splice_Rec_139808,Human_Splice_Rec_139809,Human_Splice_Rec_139832,Human_Splice_Rec_139833,Human_Splice_Rec_139856,Human_Splice_Rec_139862,Human_Splice_Rec_139863,Human_Splice_Rec_139872,Human_Splice_Rec_139873,Human_Splice_Rec_139884,Human_Splice_Rec_139885,Human_Splice_Rec_139896,Human_Splice_Rec_139897,Human_Splice_Rec_139912,Human_Splice_Rec_139913,Human_Splice_Rec_139918,Human_Splice_Rec_139919 Human_miRNA_ID_2038452,Human_miRNA_ID_2787745,Human_miRNA_ID_2817354,Human_miRNA_ID_3017434 RMVar_hsa_circ_25131,RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_280673,RMVar_hsa_circ_301144,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136672,RMVar_hsa_circ_136673,RMVar_hsa_circ_325523,RMVar_hsa_circ_276721,RMVar_hsa_circ_136677,RMVar_hsa_circ_136674,RMVar_hsa_circ_136675,RMVar_hsa_circ_271004,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_118932,RMVar_hsa_circ_136676 93922 RMVar_ID_93922 Human_SNP_ID_34774872 m1A Human chr1 - 155727714 155727714 155727714 CTAGTCACCTGGTTCAGGAAGCGCTCATTTGTAGTTTTGAAATTCTTCAGCCAGGTTGAAGCCTC CTAGTCACCTGGTTCAGGAAGCGCTCATTTGTCGTTTTGAAATTCTTCAGCCAGGTTGAAGCCTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:155727663..155731440 32194978 MeRIP-seq:(Medium) rs1481019201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 93923 RMVar_ID_93923 Human_SNP_ID_34775270 m1A Human chr1 + 155729227 155729227 155729227 TCTCTCCCAATAGGGCATAACACGGGTGAGGAACGCCACAGATGCAGTTGGAATTGTGCTGAAAG TCTCTCCCAATAGGGCATAACACGGGTGAGGAGCGCCACAGATGCAGTTGGAATTGTGCTGAAAG A G DAP3 Ensembl:ENSG00000132676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155729091..155729414 26863196 MeRIP-seq:(Medium) rs867839385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19796,Human_RBP_ID_221867,Human_RBP_ID_742717,Human_RBP_ID_802729,Human_RBP_ID_858194,Human_RBP_ID_1726664,Human_RBP_ID_3934115,Human_RBP_ID_8286846,Human_RBP_ID_10601144,Human_RBP_ID_19035510,Human_RBP_ID_22427565,Human_RBP_ID_26311916 Human_Splice_Rec_139716,Human_Splice_Rec_139744,Human_Splice_Rec_139764,Human_Splice_Rec_139796,Human_Splice_Rec_139818,Human_Splice_Rec_139842,Human_Splice_Rec_139892,Human_Splice_Rec_139904,Human_Splice_Rec_139926,Human_Splice_Rec_139934,Human_Splice_Rec_139938,Human_Splice_Rec_139944 Human_miRNA_ID_2233801,Human_miRNA_ID_2997189,Human_miRNA_ID_3027956 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_317244,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_47498,RMVar_hsa_circ_68767,RMVar_hsa_circ_136686,RMVar_hsa_circ_49600 93924 RMVar_ID_93924 Human_SNP_ID_34776017 m1A Human chr1 - 155731967 155731967 155731967 CGGGGCTTAAAGAGAGACCCAGTCTGGCTCAAAGCCGACACAATGGCGCCTCCATGCTGAAAGAA CGGGGCTTAAAGAGAGACCCAGTCTGGCTCAAGGCCGACACAATGGCGCCTCCATGCTGAAAGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:155731951..155732102 32194978 MeRIP-seq:(Medium) rs147434037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 93925 RMVar_ID_93925 Human_SNP_ID_34781114 m1A Human chr1 + 155750863 155750863 155750863 TCAGCTTACTGCAACCTCCGTCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCAGAGTAGC TCAGCTTACTGCAACCTCCGTCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTTCAGAGTAGC A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1286371422 Functional Loss SNV dbSNP153 33..33 33 - - - 93926 RMVar_ID_93926 Human_SNP_ID_34784407 m1A Human chr1 - 155763466 155763466 155763466 GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCAGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCGGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT T C GON4L Ensembl:ENSG00000116580 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155763424..155763509 26863196 MeRIP-seq:(Medium) rs607834 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5536619,Human_RBP_ID_24541699,Human_RBP_ID_26311926,Human_RBP_ID_27798605 Human_Splice_Rec_140052,Human_Splice_Rec_140114,Human_Splice_Rec_140176,Human_Splice_Rec_140240,Human_Splice_Rec_140302 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668,RMVar_hsa_circ_6614,RMVar_hsa_circ_62122,RMVar_hsa_circ_53480,RMVar_hsa_circ_268558,RMVar_hsa_circ_72995,RMVar_hsa_circ_62364,RMVar_hsa_circ_67549,RMVar_hsa_circ_104870,RMVar_hsa_circ_98494,RMVar_hsa_circ_136689,RMVar_hsa_circ_136690,RMVar_hsa_circ_101015,RMVar_hsa_circ_136691,RMVar_hsa_circ_367638,RMVar_hsa_circ_13676,RMVar_hsa_circ_67152,RMVar_hsa_circ_108586,RMVar_hsa_circ_136692 93927 RMVar_ID_93927 Human_SNP_ID_34784408 m1A Human chr1 - 155763466 155763466 155763466 GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCAGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCCGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT T G GON4L Ensembl:ENSG00000116580 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155763424..155763509 26863196 MeRIP-seq:(Medium) rs607834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5536619,Human_RBP_ID_24541699,Human_RBP_ID_26311926,Human_RBP_ID_27798605 Human_Splice_Rec_140052,Human_Splice_Rec_140114,Human_Splice_Rec_140176,Human_Splice_Rec_140240,Human_Splice_Rec_140302 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668,RMVar_hsa_circ_6614,RMVar_hsa_circ_62122,RMVar_hsa_circ_53480,RMVar_hsa_circ_268558,RMVar_hsa_circ_72995,RMVar_hsa_circ_62364,RMVar_hsa_circ_67549,RMVar_hsa_circ_104870,RMVar_hsa_circ_98494,RMVar_hsa_circ_136689,RMVar_hsa_circ_136690,RMVar_hsa_circ_101015,RMVar_hsa_circ_136691,RMVar_hsa_circ_367638,RMVar_hsa_circ_13676,RMVar_hsa_circ_67152,RMVar_hsa_circ_108586,RMVar_hsa_circ_136692 93928 RMVar_ID_93928 Human_SNP_ID_34796068 m1A Human chr1 - 155808414 155808413 155808414 TGAAAAAGAGGTAGAAATGAGGTCAGAGAGCAAGGCAAGAGCTAGATCATGAAGGTCTTAGGAAA TGAAAAAGAGGTAGAAATGAGGTCAGAGAGCA_GGCAAGAGCTAGATCATGAAGGTCTTAGGAAA CT C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155808410..155808506 26863196 MeRIP-seq:(Medium) rs1350843664 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5695555,Human_RBP_ID_10601841 RMVar_hsa_circ_18762,RMVar_hsa_circ_6614,RMVar_hsa_circ_62122,RMVar_hsa_circ_57488,RMVar_hsa_circ_60308,RMVar_hsa_circ_62302,RMVar_hsa_circ_46340,RMVar_hsa_circ_58047,RMVar_hsa_circ_29349,RMVar_hsa_circ_26499,RMVar_hsa_circ_99162,RMVar_hsa_circ_136702,RMVar_hsa_circ_88356,RMVar_hsa_circ_136703,RMVar_hsa_circ_32199,RMVar_hsa_circ_75300,RMVar_hsa_circ_269872,RMVar_hsa_circ_271767,RMVar_hsa_circ_29744,RMVar_hsa_circ_51275,RMVar_hsa_circ_136707,RMVar_hsa_circ_136708,RMVar_hsa_circ_136709,RMVar_hsa_circ_293885,RMVar_hsa_circ_348477,RMVar_hsa_circ_350519,RMVar_hsa_circ_70592,RMVar_hsa_circ_136711,RMVar_hsa_circ_18573,RMVar_hsa_circ_48407,RMVar_hsa_circ_136712 93929 RMVar_ID_93929 Human_SNP_ID_34802936 m1A Human chr1 - 155834254 155834254 155834254 ACAAGGTACTTTAAAATGTAAATTTAAAATTTAGTAGCAAAGGAGGGATAAGGATAATACCTGAG ACAAGGTACTTTAAAATGTAAATTTAAAATTTGGTAGCAAAGGAGGGATAAGGATAATACCTGAG T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155834252..155834394 26863196 MeRIP-seq:(Medium) rs1377417510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348477,RMVar_hsa_circ_136712,RMVar_hsa_circ_71077,RMVar_hsa_circ_360729 93930 RMVar_ID_93930 Human_SNP_ID_34802956 m1A Human chr1 + 155834350 155834350 155834350 ACTATTACTTCTCCAGTTGTTCCTTCTCTGTTATCTTCTTCCTCAAGGCAAGGTTGTCTTCAATC ACTATTACTTCTCCAGTTGTTCCTTCTCTGTTTTCTTCTTCCTCAAGGCAAGGTTGTCTTCAATC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155834250..155834373 26863196 MeRIP-seq:(Medium) rs934046764 Functional Loss SNV dbSNP153 33..33 33 - - - 93931 RMVar_ID_93931 Human_SNP_ID_34822003 m1A Human chr1 - 155911320 155911314 155911320 GTCAGTGCCGGAGCCTCCGCGAGTGAAGGAAGACGAAGTGCGTGACCCGACCGGCTGTGGTGTTC GTCAGTGCCGGAGCCTCCGCGAGTGAAGGAAG______TGCGTGACCCGACCGGCTGTGGTGTTC ACTTCGT A RIT1 Ensembl:ENSG00000143622 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155911222..155911350;chr1:155911216..155911353;chr1:155911241..155911375 26863196 MeRIP-seq:(Medium) rs970994124 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4074488,Human_RBP_ID_18415080,Human_RBP_ID_22780445 Human_Splice_Rec_140505,Human_Splice_Rec_140515,Human_Splice_Rec_140527,Human_Splice_Rec_140545,Human_Splice_Rec_140565,Human_Splice_Rec_140573 93932 RMVar_ID_93932 Human_SNP_ID_34827270 m1A Human chr1 - 155929662 155929662 155929662 CTCTTTGGGGAGGGCGGTGAGTGGATTCAGATAAAGAAGACCTCTAAATAGACAGGCGTCAGATA CTCTTTGGGGAGGGCGGTGAGTGGATTCAGATGAAGAAGACCTCTAAATAGACAGGCGTCAGATA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155929659..155929740 26863196 MeRIP-seq:(Medium) rs761762051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_136725,RMVar_hsa_circ_55113,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_309713,RMVar_hsa_circ_334796,RMVar_hsa_circ_286630,RMVar_hsa_circ_136738,RMVar_hsa_circ_291312,RMVar_hsa_circ_62977,RMVar_hsa_circ_136739 93933 RMVar_ID_93933 Human_SNP_ID_34827303 m1A Human chr1 + 155929763 155929763 155929763 CGAGTCAGCAAGTTCCTACATGTGAGAGGCACATCATTAATTTCTACTTCAGCTACCACCAGGTC CGAGTCAGCAAGTTCCTACATGTGAGAGGCACGTCATTAATTTCTACTTCAGCTACCACCAGGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155929669..155929767 26863196 MeRIP-seq:(Medium) rs1225653765 Functional Loss SNV dbSNP153 33..33 33 - - - 93934 RMVar_ID_93934 Human_SNP_ID_34828326 m1A Human chr1 - 155933795 155933795 155933795 CCAGCTCCAGCCCCACTTCTCTTCCTCCCGCCAGCGGCCCCAGGTGGGGAGGTCACCAGCAGTGG CCAGCTCCAGCCCCACTTCTCTTCCTCCCGCCGGCGGCCCCAGGTGGGGAGGTCACCAGCAGTGG T C KHDC4 Ensembl:ENSG00000132680 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:155933701..155933894;chr1:155933705..155933827 26863196 MeRIP-seq:(Medium) rs1367972687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19837,Human_RBP_ID_221878,Human_RBP_ID_18415081,Human_RBP_ID_18969095 Human_Splice_Rec_140582,Human_Splice_Rec_140606,Human_Splice_Rec_140654,Human_Splice_Rec_140672,Human_Splice_Rec_140690,Human_Splice_Rec_140700 RMVar_hsa_circ_117053,RMVar_hsa_circ_136725,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_62977 93935 RMVar_ID_93935 Human_SNP_ID_34828536 m1A Human chr1 + 155934387 155934387 155934387 TCGCGCTCCCCGCGGACATGGCGACCGCTTCTACTCAACCACCCGCCAACTATCCGACTACCACC TCGCGCTCCCCGCGGACATGGCGACCGCTTCTCCTCAACCACCCGCCAACTATCCGACTACCACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155934202..155934400;chr1:155934095..155934400;chr1:155934066..155934400;chr1:155934193..155934425 26863196 MeRIP-seq:(Medium) rs760111538 Functional Loss SNV dbSNP153 33..33 33 - - - 93936 RMVar_ID_93936 Human_SNP_ID_34828537 m1A Human chr1 + 155934387 155934387 155934387 TCGCGCTCCCCGCGGACATGGCGACCGCTTCTACTCAACCACCCGCCAACTATCCGACTACCACC TCGCGCTCCCCGCGGACATGGCGACCGCTTCTGCTCAACCACCCGCCAACTATCCGACTACCACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155934202..155934400;chr1:155934095..155934400;chr1:155934066..155934400;chr1:155934193..155934425 26863196 MeRIP-seq:(Medium) rs760111538 Functional Loss SNV dbSNP153 33..33 33 - - - 93937 RMVar_ID_93937 Human_SNP_ID_34828538 m1A Human chr1 + 155934387 155934387 155934387 TCGCGCTCCCCGCGGACATGGCGACCGCTTCTACTCAACCACCCGCCAACTATCCGACTACCACC TCGCGCTCCCCGCGGACATGGCGACCGCTTCTTCTCAACCACCCGCCAACTATCCGACTACCACC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:155934202..155934400;chr1:155934095..155934400;chr1:155934066..155934400;chr1:155934193..155934425 26863196 MeRIP-seq:(Medium) rs760111538 Functional Loss SNV dbSNP153 33..33 33 - - - 93938 RMVar_ID_93938 Human_SNP_ID_34833287 m1A Human chr1 - 155952816 155952816 155952816 CACTTGTTCCTTATCTGCAGTGGAGTTGCAGCAGAAGGACCGGGCACTGGTGGAGCTGCTGCGAG CACTTGTTCCTTATCTGCAGTGGAGTTGCAGCGGAAGGACCGGGCACTGGTGGAGCTGCTGCGAG T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155952679..155952866 26863196 MeRIP-seq:(Medium) rs1406748622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8754159,Human_RBP_ID_9271575,Human_RBP_ID_18966087,Human_RBP_ID_19039413,Human_RBP_ID_22560387 Human_Splice_Rec_140728,Human_Splice_Rec_140770,Human_Splice_Rec_140820,Human_Splice_Rec_140870,Human_Splice_Rec_140936,Human_Splice_Rec_140960,Human_Splice_Rec_140968 RMVar_hsa_circ_39461,RMVar_hsa_circ_29298,RMVar_hsa_circ_78625,RMVar_hsa_circ_120830,RMVar_hsa_circ_279307,RMVar_hsa_circ_122212,RMVar_hsa_circ_136740,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742 93939 RMVar_ID_93939 Human_SNP_ID_34837770 m1A Human chr1 - 155969287 155969285 155969288 CCTCTCATCCCTTCCACAGACCCGGGAAAAGGAGAAGATGAAGGAAGCCAAGGATGCCCGCTATA CCTCTCATCCCTTCCACAGACCCGGGAAAAG___AAGATGAAGGAAGCCAAGGATGCCCGCTATA TCTC T ARHGEF2 Ensembl:ENSG00000116584 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:155969213..155969554 26863196 MeRIP-seq:(Medium) rs776640726 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_857915,Human_RBP_ID_22634445,Human_RBP_ID_24748789,Human_RBP_ID_27798648 Human_Splice_Rec_140702,Human_Splice_Rec_140744,Human_Splice_Rec_140794,Human_Splice_Rec_140844,Human_Splice_Rec_140910,Human_Splice_Rec_140978,Human_Splice_Rec_140992,Human_Splice_Rec_141004,Human_Splice_Rec_141014,Human_Splice_Rec_141024,Human_Splice_Rec_141026,Human_Splice_Rec_141034 Human_miRNA_ID_2194266,Human_miRNA_ID_2216717,Human_miRNA_ID_2489437 RMVar_hsa_circ_9728,RMVar_hsa_circ_40268,RMVar_hsa_circ_73347,RMVar_hsa_circ_360636,RMVar_hsa_circ_110718,RMVar_hsa_circ_355369,RMVar_hsa_circ_136752,RMVar_hsa_circ_344834,RMVar_hsa_circ_136751,RMVar_hsa_circ_322106 93940 RMVar_ID_93940 Human_SNP_ID_34838089 m1A Human chr1 + 155970778 155970777 155970779 GGGGAAGTGTGGAGGGGCTGAGTCAACAGTGCAGGGACAGAGGGCATGGGGCTGCAGTGCCTGGG GGGGAAGTGTGGAGGGGCTGAGTCAACAGTGC__GGACAGAGGGCATGGGGCTGCAGTGCCTGGG CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155970774..155971201 26863196 MeRIP-seq:(Medium) rs1182184271 Functional Loss DEL dbSNP153 33..34 33 - - - 93941 RMVar_ID_93941 Human_SNP_ID_34839198 m1A Human chr1 + 155975576 155975576 155975576 CCTCAGCCACCAGGAGGACCCCCCATTCTTCCACTCTCCTCCAACACCGTCAGCCCTCTCAGCTC CCTCAGCCACCAGGAGGACCCCCCATTCTTCCGCTCTCCTCCAACACCGTCAGCCCTCTCAGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155975573..155975718 26863196 MeRIP-seq:(Medium) rs1009111077 Functional Loss SNV dbSNP153 33..33 33 - - - 93942 RMVar_ID_93942 Human_SNP_ID_34839746 m1A Human chr1 + 155978084 155978084 155978084 CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCAAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCGAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155978082..155978160 26863196 MeRIP-seq:(Medium) rs928596 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12214,GWAS_ID_12215,GWAS_ID_12216,GWAS_ID_12217 93943 RMVar_ID_93943 Human_SNP_ID_34839747 m1A Human chr1 + 155978084 155978084 155978084 CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCAAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCTAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155978082..155978160 26863196 MeRIP-seq:(Medium) rs928596 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12214,GWAS_ID_12215,GWAS_ID_12216,GWAS_ID_12217 93944 RMVar_ID_93944 Human_SNP_ID_34839916 m1A Human chr1 - 155978482 155978482 155978482 GCGGGCCGAACCCCTCCCCCCGCCTTCCCCCAACAATACAGGACGCCGGGGTCCGCGCCGCGTCC GCGGGCCGAACCCCTCCCCCCGCCTTCCCCCAGCAATACAGGACGCCGGGGTCCGCGCCGCGTCC T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:155978253..155978561;chr1:155970814..155978924 26863196 MeRIP-seq:(Medium) rs1276439420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074490,Human_RBP_ID_9270381,Human_RBP_ID_17072485,Human_RBP_ID_17727143,Human_RBP_ID_27835325 RMVar_hsa_circ_73347,RMVar_hsa_circ_110718,RMVar_hsa_circ_136751,RMVar_hsa_circ_322106 93945 RMVar_ID_93945 Human_SNP_ID_34847402 m1A Human chr1 + 156009336 156009336 156009336 CTATTGCCAAAGGCATTCCTGTTTATGGCTTCACGATGGAACCAAGGAGGCTCTCGCAGACTCCT CTATTGCCAAAGGCATTCCTGTTTATGGCTTCCCGATGGAACCAAGGAGGCTCTCGCAGACTCCT A C AL355388.2 Ensembl:ENSG00000285677 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156009230..156009670 26863196 MeRIP-seq:(Medium) rs1417138834 Functional Loss SNV dbSNP153 33..33 33 - - - 93946 RMVar_ID_93946 Human_SNP_ID_34847453 m1A Human chr1 - 156009550 156009550 156009550 CAGCAAGAGGAAATATGACACTCCCAAAACGAAGAAGAACTGATTGGGGCTTCCACAGCCCTCCT CAGCAAGAGGAAATATGACACTCCCAAAACGAGGAAGAACTGATTGGGGCTTCCACAGCCCTCCT T C SSR2 Ensembl:ENSG00000163479 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156009526..156009550 26863196 MeRIP-seq:(Medium) rs200258821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22873,Human_RBP_ID_1413159,Human_RBP_ID_1726802,Human_RBP_ID_3282961,Human_RBP_ID_8287046,Human_RBP_ID_18187296,Human_RBP_ID_18553063,Human_RBP_ID_19199620,Human_RBP_ID_22429721,Human_RBP_ID_22749481,Human_RBP_ID_26843601 Human_miRNA_ID_3003059 RMVar_hsa_circ_77498,RMVar_hsa_circ_87891,RMVar_hsa_circ_120703,RMVar_hsa_circ_136754,RMVar_hsa_circ_136755,RMVar_hsa_circ_136753 93947 RMVar_ID_93947 Human_SNP_ID_34847474 m1A Human chr1 + 156009625 156009625 156009625 ATAGCAGGGGGATGCCGATGGAGGGAAGGGTCATGACCCCAAAGGCTGCCCAGTCCAGCTGTAAA ATAGCAGGGGGATGCCGATGGAGGGAAGGGTCGTGACCCCAAAGGCTGCCCAGTCCAGCTGTAAA A G AL355388.2 Ensembl:ENSG00000285677 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156009576..156009625 26863196 MeRIP-seq:(Medium) rs756794782 Functional Loss SNV dbSNP153 33..33 33 - - - 93948 RMVar_ID_93948 Human_SNP_ID_34847475 m1A Human chr1 - 156009626 156009626 156009626 CTTTACAGCTGGACTGGGCAGCCTTTGGGGTCATGACCCTTCCCTCCATCGGCATCCCCCTGCTA CTTTACAGCTGGACTGGGCAGCCTTTGGGGTCTTGACCCTTCCCTCCATCGGCATCCCCCTGCTA T A SSR2 Ensembl:ENSG00000163479 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156009576..156009650 32194978 MeRIP-seq:(Medium) rs146799038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22873,Human_RBP_ID_222865,Human_RBP_ID_328433,Human_RBP_ID_803090,Human_RBP_ID_859070,Human_RBP_ID_3998722,Human_RBP_ID_5108796,Human_RBP_ID_17338478,Human_RBP_ID_17647105,Human_RBP_ID_19199624,Human_RBP_ID_22427573,Human_RBP_ID_22749481,Human_RBP_ID_22780520,Human_RBP_ID_23335877,Human_RBP_ID_27169369 Human_Splice_Rec_141064,Human_Splice_Rec_141066,Human_Splice_Rec_141074,Human_Splice_Rec_141080,Human_Splice_Rec_141086,Human_Splice_Rec_141096,Human_Splice_Rec_141106,Human_Splice_Rec_141114,Human_Splice_Rec_141122,Human_Splice_Rec_141132,Human_Splice_Rec_141140 RMVar_hsa_circ_77498,RMVar_hsa_circ_87891,RMVar_hsa_circ_120703,RMVar_hsa_circ_136754,RMVar_hsa_circ_136755,RMVar_hsa_circ_136753 93949 RMVar_ID_93949 Human_SNP_ID_34850162 m1A Human chr1 - 156020169 156020169 156020169 GGTTTGATAACTCACTTTGCTTTTTTCTCTAAAGATGAGGCTGCTGTCATTTGTGGTGTTGGCTC GGTTTGATAACTCACTTTGCTTTTTTCTCTAACGATGAGGCTGCTGTCATTTGTGGTGTTGGCTC T G SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156020126..156020175 26863196 MeRIP-seq:(Medium) rs878876479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062 93950 RMVar_ID_93950 Human_SNP_ID_34850345 m1A Human chr1 - 156020748 156020748 156020748 CGCGGTGGCTGGAGGACGTGTAACCTTGCAAGAGGCGGGAGGCGGGGGGCAGAGGTGATTGACCC CGCGGTGGCTGGAGGACGTGTAACCTTGCAAGTGGCGGGAGGCGGGGGGCAGAGGTGATTGACCC T A SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156020741..156020925 26863196 MeRIP-seq:(Medium) rs940468667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5338556 Human_Splice_Rec_141123 93951 RMVar_ID_93951 Human_SNP_ID_34855868 m1A Human chr1 + 156042729 156042729 156042729 GTTTTGACCACAAGAAACTGCCCCCAACCAAGAGGAACTCTCTCCCCAACAATACTCTCCTCATG GTTTTGACCACAAGAAACTGCCCCCAACCAAGGGGAACTCTCTCCCCAACAATACTCTCCTCATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156042727..156042803 26863196 MeRIP-seq:(Medium) rs533271095 Functional Loss SNV dbSNP153 33..33 33 - - - 93952 RMVar_ID_93952 Human_SNP_ID_34856395 m1A Human chr1 + 156045157 156045154 156045157 CAGCTCTCTTTCCTGAGTTCCCAGGTGGTCCTACCTCAGCCCCTCCCCACCGTAGGGTTTCATAT CAGCTCTCTTTCCTGAGTTCCCAGGTGGTC___CCTCAGCCCCTCCCCACCGTAGGGTTTCATAT CCTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156045151..156045216 26863196 MeRIP-seq:(Medium) rs1009464627 Functional Loss DEL dbSNP153 31..33 33 - - - 93953 RMVar_ID_93953 Human_SNP_ID_34857808 m1A Human chr1 - 156051229 156051229 156051229 CACCACGCCTGCTTCACCCGCCACCCCTGCCCAGCCCTCCACCTCTGGCAGTGCCTCTTCAGATG CACCACGCCTGCTTCACCCGCCACCCCTGCCCGGCCCTCCACCTCTGGCAGTGCCTCTTCAGATG T C UBQLN4 Ensembl:ENSG00000160803 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156051180..156051283;chr1:156051182..156051301 26863196 MeRIP-seq:(Medium) rs1477243791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222652,Human_RBP_ID_743779,Human_RBP_ID_8240223,Human_RBP_ID_22532154 Human_Splice_Rec_141192,Human_Splice_Rec_141214 RMVar_hsa_circ_38871,RMVar_hsa_circ_114812,RMVar_hsa_circ_118397,RMVar_hsa_circ_136763,RMVar_hsa_circ_136764 93954 RMVar_ID_93954 Human_SNP_ID_34857815 m1A Human chr1 - 156051246 156051246 156051246 CCTGCCTCAGCACCCTCCACCACGCCTGCTTCACCCGCCACCCCTGCCCAGCCCTCCACCTCTGG CCTGCCTCAGCACCCTCCACCACGCCTGCTTCCCCCGCCACCCCTGCCCAGCCCTCCACCTCTGG T G UBQLN4 Ensembl:ENSG00000160803 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156051201..156051277 26863196 MeRIP-seq:(Medium) rs766625825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222652,Human_RBP_ID_743779,Human_RBP_ID_8240224,Human_RBP_ID_22532154 Human_Splice_Rec_141192,Human_Splice_Rec_141214 RMVar_hsa_circ_38871,RMVar_hsa_circ_114812,RMVar_hsa_circ_118397,RMVar_hsa_circ_136763,RMVar_hsa_circ_136764 93955 RMVar_ID_93955 Human_SNP_ID_34858342 m1A Human chr1 + 156053539 156053539 156053539 TCCGGGACGCCGGACCGTCAGAGAGGCCCCCCATCTCTTCGCAGACCCCTCCTCCGCGCTCCCCC TCCGGGACGCCGGACCGTCAGAGAGGCCCCCCCTCTCTTCGCAGACCCCTCCTCCGCGCTCCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156053281..156053616 26863196 MeRIP-seq:(Medium) rs1325669030 Functional Loss SNV dbSNP153 33..33 33 - - - 93956 RMVar_ID_93956 Human_SNP_ID_34858419 m1A Human chr1 + 156053714 156053714 156053714 GCCCCGCTCGGCTCCGCCATGCCGCCGCCGCCACCCGGCCGCCCGCCAGCCCGCCCGGCTCCTCC GCCCCGCTCGGCTCCGCCATGCCGCCGCCGCCCCCCGGCCGCCCGCCAGCCCGCCCGGCTCCTCC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:156053673..156053774 26863410 MeRIP-seq:(Medium) rs973930133 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 93957 RMVar_ID_93957 Human_SNP_ID_34858436 m1A Human chr1 - 156053750 156053750 156053750 GAAGCCGAGCCGGGCCGGCCGGGCGGGCGGGGAGGAGGAGGAGCCGGGCGGGCTGGCGGGCGGCC GAAGCCGAGCCGGGCCGGCCGGGCGGGCGGGGTGGAGGAGGAGCCGGGCGGGCTGGCGGGCGGCC T A UBQLN4 Ensembl:ENSG00000160803 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr1:156053687..156053771;chr1:156053702..156053791 26863410 MeRIP-seq:(Medium) rs1333624156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22532155 93958 RMVar_ID_93958 Human_SNP_ID_34858462 m1A Human chr1 - 156053775 156053775 156053775 GAGAGAGGGGAGTGTTGGAGGCGCAGAAGCCGAGCCGGGCCGGCCGGGCGGGCGGGGAGGAGGAG GAGAGAGGGGAGTGTTGGAGGCGCAGAAGCCGGGCCGGGCCGGCCGGGCGGGCGGGGAGGAGGAG T C UBQLN4 Ensembl:ENSG00000160803 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156053710..156053809;chr1:156053709..156053807;chr1:156053183..156053825 26863196 MeRIP-seq:(Medium) rs1326950669 Functional Loss SNV dbSNP153 33..33 33 - - - 93959 RMVar_ID_93959 Human_SNP_ID_34858985 m1A Human chr1 - 156055384 156055384 156055384 CATGAGGATGAATTTGAGATTGTCTTCATTAAACGCTTGGTTCCCGTTCCGGTCGTAGGCGGCCC CATGAGGATGAATTTGAGATTGTCTTCATTAATCGCTTGGTTCCCGTTCCGGTCGTAGGCGGCCC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:156055324..156055474 26863410 MeRIP-seq:(Medium) rs760807797 Functional Loss SNV dbSNP153 33..33 33 - - - 93960 RMVar_ID_93960 Human_SNP_ID_34865549 m1A Human chr1 - 156082278 156082278 156082278 CTGCAGCCCCCCGCCCCCCGTCACCCCCGGAGAGGAGAGGAGATCTGCTTTCTTGGTTTTGCTTC CTGCAGCCCCCCGCCCCCCGTCACCCCCGGAGTGGAGAGGAGATCTGCTTTCTTGGTTTTGCTTC T A MEX3A Ensembl:ENSG00000254726 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156082268..156082443 26863196 MeRIP-seq:(Medium) rs1461189327 Functional Loss SNV dbSNP153 33..33 33 - - - 93961 RMVar_ID_93961 Human_SNP_ID_34865597 m1A Human chr1 + 156082430 156082430 156082430 CCCAGTCCGGGAGCGGCGCTCAGTGGCCCCCAATAGAGCCCAGCCCCTTCCAGCGCTCAAACTCT CCCAGTCCGGGAGCGGCGCTCAGTGGCCCCCAGTAGAGCCCAGCCCCTTCCAGCGCTCAAACTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156082278..156082461 26863196 MeRIP-seq:(Medium) rs890531583 Functional Loss SNV dbSNP153 33..33 33 - - - 93962 RMVar_ID_93962 Human_SNP_ID_34865669 m1A Human chr1 - 156082620 156082620 156082620 TCCCACTCCTAGCTTGCCCCGGAGCTGCGAGGAAAGACCGAAGGCCACATCCCTATCCTCCTCGG TCCCACTCCTAGCTTGCCCCGGAGCTGCGAGGGAAGACCGAAGGCCACATCCCTATCCTCCTCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156082614..156082722 26863196 MeRIP-seq:(Medium) rs1055065771 Functional Loss SNV dbSNP153 33..33 33 - - - 93963 RMVar_ID_93963 Human_SNP_ID_34870564 m1A Human chr1 + 156103952 156103952 156103952 CCTTCCCCGAACCCGGCCTCAGTTCCTGGGACATCCTGGCTCCATTCTTCAGCACACCCTCCCTC CCTTCCCCGAACCCGGCCTCAGTTCCTGGGACGTCCTGGCTCCATTCTTCAGCACACCCTCCCTC A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156103945..156104010 26863196 MeRIP-seq:(Medium) rs1457925398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125762 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_136772 93964 RMVar_ID_93964 Human_SNP_ID_34872928 m1A Human chr1 + 156114766 156114766 156114766 TACACCAGCCAACCCAGATCCCGAGGTCCGACAGCGCCCGGCCCAGATCCCCACGCCTGCCAGGA TACACCAGCCAACCCAGATCCCGAGGTCCGACGGCGCCCGGCCCAGATCCCCACGCCTGCCAGGA A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:156114676..156123198;chr1:156114701..156115198;chr1:156114676..156115336;chr1:156114701..156115212;chr1:156114701..156123198;chr1:156114701..156115025 26863196 MeRIP-seq:(Medium) rs1558115528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22148,Human_RBP_ID_743753,Human_RBP_ID_3998936,Human_RBP_ID_22429727 Human_Splice_Rec_141286,Human_Splice_Rec_141318 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 93965 RMVar_ID_93965 Human_SNP_ID_34873199 m1A Human chr1 + 156115240 156115240 156115240 AGGAGCGCGCCCGCCTGCAGCTGGAGCTGAGCAAAGTGCGTGAGGAGTTTAAGGAGCTGAAAGCG AGGAGCGCGCCCGCCTGCAGCTGGAGCTGAGCGAAGTGCGTGAGGAGTTTAAGGAGCTGAAAGCG A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156114751..156123198 32194978 MeRIP-seq:(Medium) rs771065515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22150,Human_RBP_ID_3934152,Human_RBP_ID_8755170,Human_RBP_ID_22427581,Human_RBP_ID_26314810 Human_Splice_Rec_141287,Human_Splice_Rec_141319,Human_Splice_Rec_141333,Human_Splice_Rec_141355,Human_Splice_Rec_141377,Human_Splice_Rec_141381 GWAS_ID_12218,GWAS_ID_12219 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 93966 RMVar_ID_93966 Human_SNP_ID_34875515 m1A Human chr1 + 156125287 156125287 156125287 AGGGAGGGACAGAGAGAAGGAGGATATATTGCAGTAGGAGGAGTTGCTGGAACAAAAGGAGGGGT AGGGAGGGACAGAGAGAAGGAGGATATATTGCCGTAGGAGGAGTTGCTGGAACAAAAGGAGGGGT A C LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156125284..156125460 26863196 MeRIP-seq:(Medium) rs1395730507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22157 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 93967 RMVar_ID_93967 Human_SNP_ID_34875516 m1A Human chr1 + 156125287 156125287 156125287 AGGGAGGGACAGAGAGAAGGAGGATATATTGCAGTAGGAGGAGTTGCTGGAACAAAAGGAGGGGT AGGGAGGGACAGAGAGAAGGAGGATATATTGCTGTAGGAGGAGTTGCTGGAACAAAAGGAGGGGT A T LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156125284..156125460 26863196 MeRIP-seq:(Medium) rs1395730507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22157 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 93968 RMVar_ID_93968 Human_SNP_ID_34875523 m1A Human chr1 + 156125326 156125326 156125326 GGAGTTGCTGGAACAAAAGGAGGGGTGGTAGGAGTGGCTTGGGGTGGCAGCAGAAGACGCCCTGT GGAGTTGCTGGAACAAAAGGAGGGGTGGTAGGTGTGGCTTGGGGTGGCAGCAGAAGACGCCCTGT A T LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:156125314..156125443 26863196 MeRIP-seq:(Medium) rs571511416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17182339 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 93969 RMVar_ID_93969 Human_SNP_ID_34876983 m1A Human chr1 - 156130775 156130775 156130775 GGGGCCATGGGTGGGCCCTGCAGGGTGGCCTCACCTTGGCCACCTGGCCCCGCAGATCATGCAGC GGGGCCATGGGTGGGCCCTGCAGGGTGGCCTCCCCTTGGCCACCTGGCCCCGCAGATCATGCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:156130567..156130825;chr1:156130601..156130830 26863196 MeRIP-seq:(Medium) rs1553264668 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_532 93970 RMVar_ID_93970 Human_SNP_ID_34877868 m1A Human chr1 - 156134500 156134500 156134500 CCACCTCACTGTAGATGTTCTTCTGGAAGTCCAGTTCCTCCTTCATGGTCTGCAGCCTGTTCTCA CCACCTCACTGTAGATGTTCTTCTGGAAGTCCTGTTCCTCCTTCATGGTCTGCAGCCTGTTCTCA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:156134451..156134525 26863196 MeRIP-seq:(Medium) rs1553265180 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_533,Clinvar_Rec_534,Clinvar_Rec_5184,Clinvar_Rec_5185 93971 RMVar_ID_93971 Human_SNP_ID_34877869 m1A Human chr1 - 156134500 156134500 156134500 CCACCTCACTGTAGATGTTCTTCTGGAAGTCCAGTTCCTCCTTCATGGTCTGCAGCCTGTTCTCA CCACCTCACTGTAGATGTTCTTCTGGAAGTCCCGTTCCTCCTTCATGGTCTGCAGCCTGTTCTCA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:156134451..156134525 26863196 MeRIP-seq:(Medium) rs1553265180 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_533,Clinvar_Rec_534,Clinvar_Rec_5184,Clinvar_Rec_5185 93972 RMVar_ID_93972 Human_SNP_ID_34877950 m1A Human chr1 - 156134764 156134764 156134764 GTTGGAGGAAGGACACAGAAACCAAAATCAGAATTAGTTCCTGGGAGGCCAAGACCCAGGGGCGG GTTGGAGGAAGGACACAGAAACCAAAATCAGACTTAGTTCCTGGGAGGCCAAGACCCAGGGGCGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156134758..156134911 26863196 MeRIP-seq:(Medium) rs996477659 Functional Loss SNV dbSNP153 33..33 33 - - - 93973 RMVar_ID_93973 Human_SNP_ID_34877974 m1A Human chr1 + 156134821 156134821 156134821 CCTCCAACCCTTCCAGGAGCTGCGTGAGACCAAGCGCCGTCATGAGACCCGACTGGTGGAGATTG CCTCCAACCCTTCCAGGAGCTGCGTGAGACCACGCGCCGTCATGAGACCCGACTGGTGGAGATTG A C LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156134801..156134875 26863196 MeRIP-seq:(Medium) rs267607584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743762,Human_RBP_ID_851815,Human_RBP_ID_8755175,Human_RBP_ID_9252991,Human_RBP_ID_9270388,Human_RBP_ID_9356991,Human_RBP_ID_19035549,Human_RBP_ID_22429736,Human_RBP_ID_23336083,Human_RBP_ID_26311979,Human_RBP_ID_27798649 Human_Splice_Rec_141292,Human_Splice_Rec_141324,Human_Splice_Rec_141338,Human_Splice_Rec_141360,Human_Splice_Rec_141386,Human_Splice_Rec_141412,Human_Splice_Rec_141438,Human_Splice_Rec_141448,Human_Splice_Rec_141464,Human_Splice_Rec_141470 GWAS_ID_12220 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_103790,RMVar_hsa_circ_136773,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_74959,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_136774 93974 RMVar_ID_93974 Human_SNP_ID_34877975 m1A Human chr1 + 156134821 156134821 156134821 CCTCCAACCCTTCCAGGAGCTGCGTGAGACCAAGCGCCGTCATGAGACCCGACTGGTGGAGATTG CCTCCAACCCTTCCAGGAGCTGCGTGAGACCAGGCGCCGTCATGAGACCCGACTGGTGGAGATTG A G LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156134801..156134875 26863196 MeRIP-seq:(Medium) rs267607584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743762,Human_RBP_ID_851815,Human_RBP_ID_8755175,Human_RBP_ID_9252991,Human_RBP_ID_9270388,Human_RBP_ID_9356991,Human_RBP_ID_19035549,Human_RBP_ID_22429736,Human_RBP_ID_23336083,Human_RBP_ID_26311979,Human_RBP_ID_27798649 Human_Splice_Rec_141292,Human_Splice_Rec_141324,Human_Splice_Rec_141338,Human_Splice_Rec_141360,Human_Splice_Rec_141386,Human_Splice_Rec_141412,Human_Splice_Rec_141438,Human_Splice_Rec_141448,Human_Splice_Rec_141464,Human_Splice_Rec_141470 GWAS_ID_12220 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_103790,RMVar_hsa_circ_136773,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_74959,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_136774 93975 RMVar_ID_93975 Human_SNP_ID_34878040 m1A Human chr1 + 156134926 156134926 156134926 TGCGCTGCAGGAACTGCGGGCCCAGCATGAGGACCAGGTGGAGCAGTATAAGAAGGAGCTGGAGA TGCGCTGCAGGAACTGCGGGCCCAGCATGAGGCCCAGGTGGAGCAGTATAAGAAGGAGCTGGAGA A C LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156134901..156134925 26863196 MeRIP-seq:(Medium) rs1240651706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743764,Human_RBP_ID_1413182,Human_RBP_ID_5136403,Human_RBP_ID_5536647,Human_RBP_ID_8228373,Human_RBP_ID_9356993,Human_RBP_ID_18455194,Human_RBP_ID_18468760,Human_RBP_ID_18966089,Human_RBP_ID_22429737,Human_RBP_ID_26309825,Human_RBP_ID_27798651 Human_Splice_Rec_141293,Human_Splice_Rec_141325,Human_Splice_Rec_141339,Human_Splice_Rec_141361,Human_Splice_Rec_141387,Human_Splice_Rec_141413,Human_Splice_Rec_141439,Human_Splice_Rec_141449,Human_Splice_Rec_141471,Human_Splice_Rec_141487,Human_Splice_Rec_141489 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_103790,RMVar_hsa_circ_136773,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_74959,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_136774 93976 RMVar_ID_93976 Human_SNP_ID_34878118 m1A Human chr1 + 156135154 156135154 156135154 AACTCAGGCCTGTGCCTCCACCCCTCCCAGTCACCACAGTCCTAACCCTTTGTCCTCCCCTCCAG AACTCAGGCCTGTGCCTCCACCCCTCCCAGTCGCCACAGTCCTAACCCTTTGTCCTCCCCTCCAG A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156135151..156135336 26863196 MeRIP-seq:(Medium) rs765005892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22634456 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_103790,RMVar_hsa_circ_136773,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_136774 93977 RMVar_ID_93977 Human_SNP_ID_34878125 m1A Human chr1 - 156135177 156135177 156135177 GCAGACTGCCTGGCATTGTCCAGCTGGAGGGGAGGACAAAGGGTTAGGACTGTGGTGACTGGGAG GCAGACTGCCTGGCATTGTCCAGCTGGAGGGGTGGACAAAGGGTTAGGACTGTGGTGACTGGGAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156135176..156135250 26863196 MeRIP-seq:(Medium) rs267607685 Functional Loss SNV dbSNP153 33..33 33 - - - 93978 RMVar_ID_93978 Human_SNP_ID_34878660 m1A Human chr1 + 156136422 156136420 156136423 TGGATGAGGAGGGCAAGTTTGTCCGGCTGCGCAACAAGTCCAATGAGGTAGGCTCCTGCTCAGGG TGGATGAGGAGGGCAAGTTTGTCCGGCTGCG___CAAGTCCAATGAGGTAGGCTCCTGCTCAGGG GCAA G LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156135871..156136465 26863196 MeRIP-seq:(Medium) rs267607550 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_98173,Human_RBP_ID_743767,Human_RBP_ID_3934154,Human_RBP_ID_8755185,Human_RBP_ID_8956686,Human_RBP_ID_22429744,Human_RBP_ID_26314817,Human_RBP_ID_27800934 Human_Splice_Rec_141299,Human_Splice_Rec_141345,Human_Splice_Rec_141367,Human_Splice_Rec_141393,Human_Splice_Rec_141419,Human_Splice_Rec_141455,Human_Splice_Rec_141477,Human_Splice_Rec_141495,Human_Splice_Rec_141507,Human_Splice_Rec_141515 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_6548,RMVar_hsa_circ_126432,RMVar_hsa_circ_136774,RMVar_hsa_circ_73140,RMVar_hsa_circ_136776 93979 RMVar_ID_93979 Human_SNP_ID_34878663 m1A Human chr1 + 156136422 156136422 156136422 TGGATGAGGAGGGCAAGTTTGTCCGGCTGCGCAACAAGTCCAATGAGGTAGGCTCCTGCTCAGGG TGGATGAGGAGGGCAAGTTTGTCCGGCTGCGCGACAAGTCCAATGAGGTAGGCTCCTGCTCAGGG A G LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156135871..156136465 26863196 MeRIP-seq:(Medium) rs267607599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98173,Human_RBP_ID_743767,Human_RBP_ID_3934154,Human_RBP_ID_8755185,Human_RBP_ID_8956686,Human_RBP_ID_22429744,Human_RBP_ID_26314817,Human_RBP_ID_27800934 Human_Splice_Rec_141299,Human_Splice_Rec_141345,Human_Splice_Rec_141367,Human_Splice_Rec_141393,Human_Splice_Rec_141419,Human_Splice_Rec_141455,Human_Splice_Rec_141477,Human_Splice_Rec_141495,Human_Splice_Rec_141507,Human_Splice_Rec_141515 Clinvar_Rec_535 GWAS_ID_12221 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_6548,RMVar_hsa_circ_126432,RMVar_hsa_circ_136774,RMVar_hsa_circ_73140,RMVar_hsa_circ_136776 93980 RMVar_ID_93980 Human_SNP_ID_34878664 m1A Human chr1 + 156136422 156136422 156136422 TGGATGAGGAGGGCAAGTTTGTCCGGCTGCGCAACAAGTCCAATGAGGTAGGCTCCTGCTCAGGG TGGATGAGGAGGGCAAGTTTGTCCGGCTGCGCTACAAGTCCAATGAGGTAGGCTCCTGCTCAGGG A T LMNA Ensembl:ENSG00000160789 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156135871..156136465 26863196 MeRIP-seq:(Medium) rs267607599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98173,Human_RBP_ID_743767,Human_RBP_ID_3934154,Human_RBP_ID_8755185,Human_RBP_ID_8956686,Human_RBP_ID_22429744,Human_RBP_ID_26314817,Human_RBP_ID_27800934 Human_Splice_Rec_141299,Human_Splice_Rec_141345,Human_Splice_Rec_141367,Human_Splice_Rec_141393,Human_Splice_Rec_141419,Human_Splice_Rec_141455,Human_Splice_Rec_141477,Human_Splice_Rec_141495,Human_Splice_Rec_141507,Human_Splice_Rec_141515 Clinvar_Rec_535 GWAS_ID_12221 RMVar_hsa_circ_3076,RMVar_hsa_circ_41174,RMVar_hsa_circ_8019,RMVar_hsa_circ_21469,RMVar_hsa_circ_5856,RMVar_hsa_circ_94333,RMVar_hsa_circ_6548,RMVar_hsa_circ_126432,RMVar_hsa_circ_136774,RMVar_hsa_circ_73140,RMVar_hsa_circ_136776 93981 RMVar_ID_93981 Human_SNP_ID_34878671 m1A Human chr1 - 156136438 156136438 156136438 GCTGTATCCCCTTAGACCCTGAGCAGGAGCCTACCTCATTGGACTTGTTGCGCAGCCGGACAAAC GCTGTATCCCCTTAGACCCTGAGCAGGAGCCTCCCTCATTGGACTTGTTGCGCAGCCGGACAAAC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156136401..156136450 32194978 MeRIP-seq:(Medium) rs1553265924 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_536 93982 RMVar_ID_93982 Human_SNP_ID_34879126 m1A Human chr1 - 156137673 156137673 156137673 CGTCGTCCTCAACCACAGTCACTGAGCGCACCAGCTTGCGCATGGCCACTTCCTGGTGGGGACAT CGTCGTCCTCAACCACAGTCACTGAGCGCACCGGCTTGCGCATGGCCACTTCCTGGTGGGGACAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156137651..156137821 32194978 MeRIP-seq:(Medium) rs886042329 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_537 93983 RMVar_ID_93983 Human_SNP_ID_34879339 m1A Human chr1 - 156138477 156138476 156138477 CCGAGCTGCTGCAGTGGGAGCCCTGGGAAGGGAGACAAGGCTCAGGCGGGACGGCGAGTCTGGGA CCGAGCTGCTGCAGTGGGAGCCCTGGGAAGGG_GACAAGGCTCAGGCGGGACGGCGAGTCTGGGA CT C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156138476..156138525 26863196 MeRIP-seq:(Medium) rs772968294 Functional Loss DEL dbSNP153 33..33 33 - - - 93984 RMVar_ID_93984 Human_SNP_ID_34879378 m1A Human chr1 - 156138551 156138551 156138551 TGCCTTGTCGGCAGGCTGCCCGCAGGTCCCGCACAGCACGGTGCGCGAGCGCAGGTTGTACTCAG TGCCTTGTCGGCAGGCTGCCCGCAGGTCCCGCGCAGCACGGTGCGCGAGCGCAGGTTGTACTCAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156138526..156138550 26863196 MeRIP-seq:(Medium) rs267607621 Functional Loss SNV dbSNP153 33..33 33 - - - 93985 RMVar_ID_93985 Human_SNP_ID_34879795 m1A Human chr1 - 156139828 156139828 156139828 GAGCCCACCCAGGGTCTAAAGCTAGGGAAGGCAGCTCAAACTCACCTTTCTTCTCCCTTCTTCCA GAGCCCACCCAGGGTCTAAAGCTAGGGAAGGCGGCTCAAACTCACCTTTCTTCTCCCTTCTTCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156139531..156140025;chr1:156139726..156140000;chr1:156139726..156140025 26863196 MeRIP-seq:(Medium) rs921268252 Functional Loss SNV dbSNP153 33..33 33 - - - 93986 RMVar_ID_93986 Human_SNP_ID_34893761 m1A Human chr1 + 156194166 156194166 156194166 ATGCGACCGGCAGACGGCATTCGCTGGGAACGACGGATAGACTGGGGGCTGCGGCCTAGAGGTCC ATGCGACCGGCAGACGGCATTCGCTGGGAACGGCGGATAGACTGGGGGCTGCGGCCTAGAGGTCC A G SLC25A44 Ensembl:ENSG00000160785 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156194117..156194285 26863196 MeRIP-seq:(Medium) rs79014111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224382,Human_RBP_ID_328582,Human_RBP_ID_745345,Human_RBP_ID_22871420,Human_RBP_ID_26314818 Human_Splice_Rec_141759,Human_Splice_Rec_141765 93987 RMVar_ID_93987 Human_SNP_ID_34898090 m1A Human chr1 + 156213060 156213060 156213060 AGTAGCGCCAATCTAGGCAGCGGCTGTGAGGAAAAAAGGCATGAGGGGTCGTCTTCGGAATCTGT AGTAGCGCCAATCTAGGCAGCGGCTGTGAGGAGAAAAGGCATGAGGGGTCGTCTTCGGAATCTGT A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156213001..156213130;chr1:156213001..156213075 26863196 MeRIP-seq:(Medium) rs369050130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328622,Human_RBP_ID_10604849,Human_RBP_ID_18428685,Human_RBP_ID_22431015,Human_RBP_ID_22870973 93988 RMVar_ID_93988 Human_SNP_ID_34899128 m1A Human chr1 + 156216731 156216726 156216732 GGCGCCCGGGGCGGCCGCGACAACCCCACCCCACTGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC GGCGCCCGGGGCGGCCGCGACAACCCCA______TGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC ACCCCAC A PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1217887544 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_25410,Human_RBP_ID_269107,Human_RBP_ID_1074460,Human_RBP_ID_1149943,Human_RBP_ID_1344993,Human_RBP_ID_1413215,Human_RBP_ID_2096779,Human_RBP_ID_3283026,Human_RBP_ID_4082664,Human_RBP_ID_5155738,Human_RBP_ID_5272919,Human_RBP_ID_8240234,Human_RBP_ID_8287149,Human_RBP_ID_8735691,Human_RBP_ID_10604989,Human_RBP_ID_18553134,Human_RBP_ID_19200408,Human_RBP_ID_22129135,Human_RBP_ID_22780547,Human_RBP_ID_22848117,Human_RBP_ID_23123115,Human_RBP_ID_23144834,Human_RBP_ID_23303865,Human_RBP_ID_26389885,Human_RBP_ID_26578617,Human_RBP_ID_26843688,Human_RBP_ID_27169487 93989 RMVar_ID_93989 Human_SNP_ID_34899131 m1A Human chr1 + 156216731 156216731 156216731 GGCGCCCGGGGCGGCCGCGACAACCCCACCCCACTGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC GGCGCCCGGGGCGGCCGCGACAACCCCACCCCGCTGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4119260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25410,Human_RBP_ID_269107,Human_RBP_ID_1074460,Human_RBP_ID_1149943,Human_RBP_ID_1344993,Human_RBP_ID_1413215,Human_RBP_ID_2096779,Human_RBP_ID_3283026,Human_RBP_ID_4082664,Human_RBP_ID_5155738,Human_RBP_ID_5272919,Human_RBP_ID_8240234,Human_RBP_ID_8287149,Human_RBP_ID_8735691,Human_RBP_ID_10604989,Human_RBP_ID_18553134,Human_RBP_ID_19200408,Human_RBP_ID_22129135,Human_RBP_ID_22780547,Human_RBP_ID_22848117,Human_RBP_ID_23123115,Human_RBP_ID_23144834,Human_RBP_ID_23303865,Human_RBP_ID_26389885,Human_RBP_ID_26578617,Human_RBP_ID_26843688,Human_RBP_ID_27169487 93990 RMVar_ID_93990 Human_SNP_ID_34904129 m1A Human chr1 + 156236386 156236386 156236386 GGACACCCTGCGGCGCCATGTGCAGAAACAGGAGGCCGAGAACCAGCAGCTGGCAGATGCCGTCC GGACACCCTGCGGCGCCATGTGCAGAAACAGGGGGCCGAGAACCAGCAGCTGGCAGATGCCGTCC A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156236335..156236511 26863196 MeRIP-seq:(Medium) rs761830699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_141784,Human_Splice_Rec_141785,Human_Splice_Rec_141796,Human_Splice_Rec_141797,Human_Splice_Rec_141804,Human_Splice_Rec_141805,Human_Splice_Rec_141826,Human_Splice_Rec_141827,Human_Splice_Rec_141842,Human_Splice_Rec_141843,Human_Splice_Rec_141848,Human_Splice_Rec_141854,Human_Splice_Rec_141855,Human_Splice_Rec_141862,Human_Splice_Rec_141863 RMVar_hsa_circ_50170,RMVar_hsa_circ_296234,RMVar_hsa_circ_136785 93991 RMVar_ID_93991 Human_SNP_ID_34904137 m1A Human chr1 + 156236398 156236398 156236398 GCGCCATGTGCAGAAACAGGAGGCCGAGAACCAGCAGCTGGCAGATGCCGTCCTGGCAGGGCGGA GCGCCATGTGCAGAAACAGGAGGCCGAGAACCGGCAGCTGGCAGATGCCGTCCTGGCAGGGCGGA A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156235982..156236551 26863196 MeRIP-seq:(Medium) rs764380670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_141785,Human_Splice_Rec_141796,Human_Splice_Rec_141797,Human_Splice_Rec_141805,Human_Splice_Rec_141826,Human_Splice_Rec_141827,Human_Splice_Rec_141843,Human_Splice_Rec_141855,Human_Splice_Rec_141863 RMVar_hsa_circ_50170,RMVar_hsa_circ_296234,RMVar_hsa_circ_136785 93992 RMVar_ID_93992 Human_SNP_ID_34905034 m1A Human chr1 + 156239604 156239604 156239604 CTGGTTGCTGTGCTGAGGGAGCCTGAGTGAGGAGACCGCCAGCCCCAGAAGCAGAGGGCAGTCAA CTGGTTGCTGTGCTGAGGGAGCCTGAGTGAGGGGACCGCCAGCCCCAGAAGCAGAGGGCAGTCAA A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156239526..156240050;chr1:156239512..156240050 26863196 MeRIP-seq:(Medium) rs1404762646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855378,Human_RBP_ID_5109254,Human_RBP_ID_5136409,Human_RBP_ID_17646168,Human_RBP_ID_19039442,Human_RBP_ID_22429754,Human_RBP_ID_22637637,Human_RBP_ID_27835328 Human_Splice_Rec_141828,Human_Splice_Rec_141844,Human_Splice_Rec_141856,Human_Splice_Rec_141864 93993 RMVar_ID_93993 Human_SNP_ID_34905035 m1A Human chr1 + 156239604 156239604 156239604 CTGGTTGCTGTGCTGAGGGAGCCTGAGTGAGGAGACCGCCAGCCCCAGAAGCAGAGGGCAGTCAA CTGGTTGCTGTGCTGAGGGAGCCTGAGTGAGGTGACCGCCAGCCCCAGAAGCAGAGGGCAGTCAA A T PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156239526..156240050;chr1:156239512..156240050 26863196 MeRIP-seq:(Medium) rs1404762646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855378,Human_RBP_ID_5109254,Human_RBP_ID_5136409,Human_RBP_ID_17646168,Human_RBP_ID_19039442,Human_RBP_ID_22429754,Human_RBP_ID_22637637,Human_RBP_ID_27835328 Human_Splice_Rec_141828,Human_Splice_Rec_141844,Human_Splice_Rec_141856,Human_Splice_Rec_141864 93994 RMVar_ID_93994 Human_SNP_ID_34908599 m1A Human chr1 - 156250000 156250000 156250000 CTGTTAGAGAAGCAAGGCCTGGAGTGGCCTGCACCGAGTAGCAGGGTCAGGGTTCGTGTGCTCCT CTGTTAGAGAAGCAAGGCCTGGAGTGGCCTGCGCCGAGTAGCAGGGTCAGGGTTCGTGTGCTCCT T C SMG5 Ensembl:ENSG00000198952 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156249951..156250200 32194978 MeRIP-seq:(Medium) rs1273038921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8228056,Human_RBP_ID_10605861,Human_RBP_ID_22848136 Human_miRNA_ID_1266617 RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136786,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_81768,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787 93995 RMVar_ID_93995 Human_SNP_ID_34908857 m1A Human chr1 - 156250949 156250948 156250949 CCTAGACAGCTGCAAACAGCTGACTCTGGCCCAGGGGGCAGGTGAGGAGGATCCGAGTGGCATGG CCTAGACAGCTGCAAACAGCTGACTCTGGCCC_GGGGGCAGGTGAGGAGGATCCGAGTGGCATGG CT C SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156250901..156250975 32194978 MeRIP-seq:(Medium) rs1428333171 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1502,Human_RBP_ID_1726860,Human_RBP_ID_5109912,Human_RBP_ID_5696628,Human_RBP_ID_9356997,Human_RBP_ID_10605892,Human_RBP_ID_18553219,Human_RBP_ID_22780600,Human_RBP_ID_22871422,Human_RBP_ID_26386532 Human_Splice_Rec_142110,Human_Splice_Rec_142111,Human_Splice_Rec_142113 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136786,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_81768,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787 93996 RMVar_ID_93996 Human_SNP_ID_34908858 m1A Human chr1 - 156250949 156250949 156250949 CCTAGACAGCTGCAAACAGCTGACTCTGGCCCAGGGGGCAGGTGAGGAGGATCCGAGTGGCATGG CCTAGACAGCTGCAAACAGCTGACTCTGGCCCCGGGGGCAGGTGAGGAGGATCCGAGTGGCATGG T G SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156250901..156250975 32194978 MeRIP-seq:(Medium) rs200665589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1502,Human_RBP_ID_1726860,Human_RBP_ID_5109912,Human_RBP_ID_5696628,Human_RBP_ID_9356997,Human_RBP_ID_10605892,Human_RBP_ID_18553219,Human_RBP_ID_22780600,Human_RBP_ID_22871422,Human_RBP_ID_26386532 Human_Splice_Rec_142110,Human_Splice_Rec_142111,Human_Splice_Rec_142113 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136786,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_81768,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787 93997 RMVar_ID_93997 Human_SNP_ID_34909241 m1A Human chr1 + 156252406 156252406 156252406 GACCCAGGGCTCAGCACAGGTCCAGCCAGGCCACACTCACCTGTTTCCTTTTTTAAACTCTGCCT GACCCAGGGCTCAGCACAGGTCCAGCCAGGCCGCACTCACCTGTTTCCTTTTTTAAACTCTGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156252401..156252450 26863196 MeRIP-seq:(Medium) rs984889064 Functional Loss SNV dbSNP153 33..33 33 - - - 93998 RMVar_ID_93998 Human_SNP_ID_34911290 m1A Human chr1 - 156260602 156260602 156260602 CTGCCCAGGCCTGGCCTTGTGTCCTGAGGTCCAAGATCTTCTTGAAGGTTGTGAACTGCCTGACC CTGCCCAGGCCTGGCCTTGTGTCCTGAGGTCCGAGATCTTCTTGAAGGTTGTGAACTGCCTGACC T C SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156260551..156260650 32194978 MeRIP-seq:(Medium) rs1335110674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413295,Human_RBP_ID_3999254,Human_RBP_ID_18553228,Human_RBP_ID_23255387,Human_RBP_ID_23336251 Human_Splice_Rec_142098 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787,RMVar_hsa_circ_3375,RMVar_hsa_circ_85980,RMVar_hsa_circ_78121,RMVar_hsa_circ_121354,RMVar_hsa_circ_136792,RMVar_hsa_circ_136793,RMVar_hsa_circ_33818,RMVar_hsa_circ_356241,RMVar_hsa_circ_136794,RMVar_hsa_circ_350515,RMVar_hsa_circ_37355,RMVar_hsa_circ_331386,RMVar_hsa_circ_339581,RMVar_hsa_circ_38583 93999 RMVar_ID_93999 Human_SNP_ID_34912065 m1A Human chr1 - 156263358 156263358 156263358 GTCAGTCCACTCCATTGCCCCTGTCAGGTCCCAGGGTCTTGGAGGAGGGGATGAGCCAGGATGGG GTCAGTCCACTCCATTGCCCCTGTCAGGTCCCGGGGTCTTGGAGGAGGGGATGAGCCAGGATGGG T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156263354..156263459 26863196 MeRIP-seq:(Medium) rs376867760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5335986 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787,RMVar_hsa_circ_85980,RMVar_hsa_circ_78121,RMVar_hsa_circ_121354,RMVar_hsa_circ_136792,RMVar_hsa_circ_136793,RMVar_hsa_circ_33818,RMVar_hsa_circ_356241,RMVar_hsa_circ_136794,RMVar_hsa_circ_350515,RMVar_hsa_circ_37355,RMVar_hsa_circ_339581,RMVar_hsa_circ_38583,RMVar_hsa_circ_358939 94000 RMVar_ID_94000 Human_SNP_ID_34912114 m1A Human chr1 - 156263493 156263493 156263493 GCTCCTGTCGGAATGAGCGCAGCATCCAGGAGAAGCTTCAGGTCCTGATGGCCGAAGGTCTGCTT GCTCCTGTCGGAATGAGCGCAGCATCCAGGAGGAGCTTCAGGTCCTGATGGCCGAAGGTCTGCTT T C SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156263401..156263500 32194978 MeRIP-seq:(Medium) rs200093957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328677,Human_RBP_ID_1726864,Human_RBP_ID_5536656,Human_RBP_ID_8735719,Human_RBP_ID_9266447,Human_RBP_ID_23336255 Human_Splice_Rec_142094,Human_Splice_Rec_142095 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787,RMVar_hsa_circ_85980,RMVar_hsa_circ_78121,RMVar_hsa_circ_121354,RMVar_hsa_circ_136792,RMVar_hsa_circ_136793,RMVar_hsa_circ_33818,RMVar_hsa_circ_356241,RMVar_hsa_circ_136794,RMVar_hsa_circ_350515,RMVar_hsa_circ_37355,RMVar_hsa_circ_339581,RMVar_hsa_circ_38583,RMVar_hsa_circ_300204,RMVar_hsa_circ_358939 94001 RMVar_ID_94001 Human_SNP_ID_34912972 m1A Human chr1 - 156266138 156266136 156266138 CCAGTGAGGGCTCAGACAGTGGCTCTGACAAGAGTCTTGAAGGTGGGGGAACGGCCTTTGATGCT CCAGTGAGGGCTCAGACAGTGGCTCTGACAAG__TCTTGAAGGTGGGGGAACGGCCTTTGATGCT ACT A SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156266088..156266322 26863196 MeRIP-seq:(Medium) rs1341800750 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23828,Human_RBP_ID_1726866,Human_RBP_ID_8754176,Human_RBP_ID_9270399,Human_RBP_ID_23205381 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_136789,RMVar_hsa_circ_85980,RMVar_hsa_circ_78121,RMVar_hsa_circ_136793,RMVar_hsa_circ_33818,RMVar_hsa_circ_136794,RMVar_hsa_circ_350515,RMVar_hsa_circ_37355,RMVar_hsa_circ_38583,RMVar_hsa_circ_293195,RMVar_hsa_circ_300204,RMVar_hsa_circ_358939,RMVar_hsa_circ_312873,RMVar_hsa_circ_375623,RMVar_hsa_circ_60394,RMVar_hsa_circ_80134,RMVar_hsa_circ_136795,RMVar_hsa_circ_136796 94002 RMVar_ID_94002 Human_SNP_ID_34912973 m1A Human chr1 - 156266138 156266138 156266138 CCAGTGAGGGCTCAGACAGTGGCTCTGACAAGAGTCTTGAAGGTGGGGGAACGGCCTTTGATGCT CCAGTGAGGGCTCAGACAGTGGCTCTGACAAGTGTCTTGAAGGTGGGGGAACGGCCTTTGATGCT T A SMG5 Ensembl:ENSG00000198952 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156266088..156266322 26863196 MeRIP-seq:(Medium) rs1469529768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23828,Human_RBP_ID_1726866,Human_RBP_ID_8754176,Human_RBP_ID_9270399,Human_RBP_ID_23205381 RMVar_hsa_circ_34234,RMVar_hsa_circ_90375,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_136789,RMVar_hsa_circ_85980,RMVar_hsa_circ_78121,RMVar_hsa_circ_136793,RMVar_hsa_circ_33818,RMVar_hsa_circ_136794,RMVar_hsa_circ_350515,RMVar_hsa_circ_37355,RMVar_hsa_circ_38583,RMVar_hsa_circ_293195,RMVar_hsa_circ_300204,RMVar_hsa_circ_358939,RMVar_hsa_circ_312873,RMVar_hsa_circ_375623,RMVar_hsa_circ_60394,RMVar_hsa_circ_80134,RMVar_hsa_circ_136795,RMVar_hsa_circ_136796 94003 RMVar_ID_94003 Human_SNP_ID_34917488 m1A Human chr1 + 156282780 156282765 156282780 CGTCTCCGGCCGTAGCCGCAGCCGCCGCCGCCACCGGCCCTGCTCGGCCGCCATCGCTGTGAGGC CGTCTCCGGCCGTAGCCG_______________CCGGCCCTGCTCGGCCGCCATCGCTGTGAGGC GCAGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156282363..156282850;chr1:156282626..156282905 26863196 MeRIP-seq:(Medium) rs976735510 Functional Loss DEL dbSNP153 19..33 33 - - - 94004 RMVar_ID_94004 Human_SNP_ID_34920421 m1A Human chr1 - 156293448 156293448 156293448 CCCTGCCAAGCTTCCCCTCTTCATCCTGCCTTAGCATACTCTCTTCCCCAGTCACCCATTGTCCG CCCTGCCAAGCTTCCCCTCTTCATCCTGCCTTGGCATACTCTCTTCCCCAGTCACCCATTGTCCG T C GLMP Ensembl:ENSG00000198715 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156293399..156293528 26863196 MeRIP-seq:(Medium) rs183754290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18930104 RMVar_hsa_circ_119259,RMVar_hsa_circ_83568,RMVar_hsa_circ_116526,RMVar_hsa_circ_99684,RMVar_hsa_circ_136805,RMVar_hsa_circ_136806,RMVar_hsa_circ_136804,RMVar_hsa_circ_136807 94005 RMVar_ID_94005 Human_SNP_ID_34920742 m1A Human chr1 + 156294438 156294437 156294439 CGTTCATGGGGTGGCCTTGAAATGTGGCACTCAGGGTGGCAGGATCCAATGAATCAGTGATGTTG CGTTCATGGGGTGGCCTTGAAATGTGGCACTC__GGTGGCAGGATCCAATGAATCAGTGATGTTG CAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156294300..156294438 26863196 MeRIP-seq:(Medium) rs1346702216 Functional Loss DEL dbSNP153 33..34 33 - - - 94006 RMVar_ID_94006 Human_SNP_ID_34925116 m1A Human chr1 - 156309199 156309195 156309199 CAAGGCGGGGCTCCTGATGCTGGCCAGGAGTGAGTGCTAGGCAAGGCTACTTCAATGCACAGAAC CAAGGCGGGGCTCCTGATGCTGGCCAGGAGTG____CTAGGCAAGGCTACTTCAATGCACAGAAC GCACT G CCT3 Ensembl:ENSG00000163468 Protein coding stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156309026..156309200 32194978 MeRIP-seq:(Medium) rs753057668 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_328743,Human_RBP_ID_744062,Human_RBP_ID_1726903,Human_RBP_ID_3283105,Human_RBP_ID_4082713,Human_RBP_ID_5137660,Human_RBP_ID_5696943,Human_RBP_ID_8287303,Human_RBP_ID_8735764,Human_RBP_ID_8956720,Human_RBP_ID_17212879,Human_RBP_ID_17446658,Human_RBP_ID_22427607,Human_RBP_ID_23336377,Human_RBP_ID_26369633,Human_RBP_ID_27169573 Human_miRNA_ID_1387309,Human_miRNA_ID_2707718 RMVar_hsa_circ_123798,RMVar_hsa_circ_136809,RMVar_hsa_circ_91850,RMVar_hsa_circ_118445,RMVar_hsa_circ_136810,RMVar_hsa_circ_136811 94007 RMVar_ID_94007 Human_SNP_ID_34925140 m1A Human chr1 + 156309272 156309272 156309272 GGTCATCGCCTTTCTTTTTGTGGCCTGAAACGATGTCATCAATTCGCAGTAGCAGAACTGCCGTC GGTCATCGCCTTTCTTTTTGTGGCCTGAAACGGTGTCATCAATTCGCAGTAGCAGAACTGCCGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156309118..156309345;chr1:156309149..156309334;chr1:156309169..156309349 26863196 MeRIP-seq:(Medium) rs1219421492 Functional Loss SNV dbSNP153 33..33 33 - - - 94008 RMVar_ID_94008 Human_SNP_ID_34925538 m1A Human chr1 - 156310619 156310619 156310619 AAATGGTGAGACGGGTACTTTGGTGGACATGAAGGAACTGGGCATATGGGAGCCATTGGCTGTGA AAATGGTGAGACGGGTACTTTGGTGGACATGAGGGAACTGGGCATATGGGAGCCATTGGCTGTGA T C CCT3 Ensembl:ENSG00000163468 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156310527..156310622 26863196 MeRIP-seq:(Medium) rs199530951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22828,Human_RBP_ID_328756,Human_RBP_ID_971728,Human_RBP_ID_1413344,Human_RBP_ID_1726906,Human_RBP_ID_3283107,Human_RBP_ID_5136412,Human_RBP_ID_5433020,Human_RBP_ID_5696949,Human_RBP_ID_8287307,Human_RBP_ID_8735767,Human_RBP_ID_10607138,Human_RBP_ID_17446659,Human_RBP_ID_18553313,Human_RBP_ID_22428638,Human_RBP_ID_22780648,Human_RBP_ID_23206149,Human_RBP_ID_23336381,Human_RBP_ID_24528790 Human_Splice_Rec_142276,Human_Splice_Rec_142277,Human_Splice_Rec_142298,Human_Splice_Rec_142299,Human_Splice_Rec_142322,Human_Splice_Rec_142323,Human_Splice_Rec_142331,Human_Splice_Rec_142358,Human_Splice_Rec_142359,Human_Splice_Rec_142386,Human_Splice_Rec_142387 Human_miRNA_ID_256281,Human_miRNA_ID_260074,Human_miRNA_ID_585315,Human_miRNA_ID_2194268,Human_miRNA_ID_2213519 RMVar_hsa_circ_123798,RMVar_hsa_circ_20416,RMVar_hsa_circ_136809,RMVar_hsa_circ_91850,RMVar_hsa_circ_118445,RMVar_hsa_circ_136810,RMVar_hsa_circ_136811,RMVar_hsa_circ_340707,RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_53778,RMVar_hsa_circ_136813,RMVar_hsa_circ_15909 94009 RMVar_ID_94009 Human_SNP_ID_34925674 m1A Human chr1 + 156311048 156311048 156311048 CTCTAGGGCCTGGGCAACAGCCCTGTATGGCCATTGTTCCACACCAGTCATGGCCTTGGATTTTT CTCTAGGGCCTGGGCAACAGCCCTGTATGGCCGTTGTTCCACACCAGTCATGGCCTTGGATTTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156310997..156311142 26863196 MeRIP-seq:(Medium) rs150509620 Functional Loss SNV dbSNP153 33..33 33 - - - 94010 RMVar_ID_94010 Human_SNP_ID_34925723 m1A Human chr1 - 156311193 156311193 156311193 GGCTTCATACTGTCTGTTTGCTTCTCCAAGGAAGTAGAACGCAACCTCCAGGATGCCATGCAAGT GGCTTCATACTGTCTGTTTGCTTCTCCAAGGAGGTAGAACGCAACCTCCAGGATGCCATGCAAGT T C CCT3 Ensembl:ENSG00000163468 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156310951..156311200 32194978 MeRIP-seq:(Medium) rs770438547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413354,Human_RBP_ID_10607159,Human_RBP_ID_17764143,Human_RBP_ID_26767578 Human_Splice_Rec_142274,Human_Splice_Rec_142296,Human_Splice_Rec_142320,Human_Splice_Rec_142356,Human_Splice_Rec_142384 RMVar_hsa_circ_20416,RMVar_hsa_circ_136809,RMVar_hsa_circ_91850,RMVar_hsa_circ_118445,RMVar_hsa_circ_136810,RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_53778,RMVar_hsa_circ_136813,RMVar_hsa_circ_15909 94011 RMVar_ID_94011 Human_SNP_ID_34927427 m1A Human chr1 + 156317367 156317367 156317367 TGCCAAACATGAGGGGAGAAAACAAATCACCCACCCTCGTCTACCTCAAAGGTAGGCTGGAAAAA TGCCAAACATGAGGGGAGAAAACAAATCACCCGCCCTCGTCTACCTCAAAGGTAGGCTGGAAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156317365..156317590 26863196 MeRIP-seq:(Medium) rs766917682 Functional Loss SNV dbSNP153 33..33 33 - - - 94012 RMVar_ID_94012 Human_SNP_ID_34927446 m1A Human chr1 + 156317403 156317403 156317403 TCGTCTACCTCAAAGGTAGGCTGGAAAAAGTAACAAAGTCCCACCTGAGATGCCCTTTTCAGTGA TCGTCTACCTCAAAGGTAGGCTGGAAAAAGTATCAAAGTCCCACCTGAGATGCCCTTTTCAGTGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156317401..156317550 32194978 MeRIP-seq:(Medium) rs1432367388 Functional Loss SNV dbSNP153 33..33 33 - - - 94013 RMVar_ID_94013 Human_SNP_ID_34927876 m1A Human chr1 + 156319001 156319001 156319001 TCATGACTCCACGCAAGACACAGGAGTCTTCAATGATGCCTCCAGGTATCTGAACAAAAGACAAC TCATGACTCCACGCAAGACACAGGAGTCTTCAGTGATGCCTCCAGGTATCTGAACAAAAGACAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156318851..156319000 32194978 MeRIP-seq:(Medium) rs758871657 Functional Loss SNV dbSNP153 33..33 33 - - - 94014 RMVar_ID_94014 Human_SNP_ID_34928441 m1A Human chr1 + 156321023 156321023 156321023 GCATCATATCACTGTCACTGATGTCGACTGGGATACTAGAGAAAAGAAAACCAGACGATATGTGA GCATCATATCACTGTCACTGATGTCGACTGGGGTACTAGAGAAAAGAAAACCAGACGATATGTGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156320876..156321050 32194978 MeRIP-seq:(Medium) rs1452443917 Functional Loss SNV dbSNP153 33..33 33 - - - 94015 RMVar_ID_94015 Human_SNP_ID_34929518 m1A Human chr1 - 156325027 156325027 156325027 TCCTGGAGCAGCAGATGCACCCAACAGTGGTGATCAGTGCTTACCGCAAGGCATTGGATGATATG TCCTGGAGCAGCAGATGCACCCAACAGTGGTGGTCAGTGCTTACCGCAAGGCATTGGATGATATG T C CCT3 Ensembl:ENSG00000163468 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs757799696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22846,Human_RBP_ID_328796,Human_RBP_ID_1149977,Human_RBP_ID_1413381,Human_RBP_ID_1726941,Human_RBP_ID_3999459,Human_RBP_ID_8287341,Human_RBP_ID_9271599,Human_RBP_ID_9357010,Human_RBP_ID_17727384,Human_RBP_ID_18416007,Human_RBP_ID_22780666,Human_RBP_ID_23336413,Human_RBP_ID_26309830,Human_RBP_ID_27800935 Human_Splice_Rec_142262,Human_Splice_Rec_142263,Human_Splice_Rec_142284,Human_Splice_Rec_142285,Human_Splice_Rec_142308,Human_Splice_Rec_142309,Human_Splice_Rec_142325,Human_Splice_Rec_142344,Human_Splice_Rec_142345,Human_Splice_Rec_142372,Human_Splice_Rec_142373,Human_Splice_Rec_142398,Human_Splice_Rec_142399,Human_Splice_Rec_142412,Human_Splice_Rec_142413,Human_Splice_Rec_142418,Human_Splice_Rec_142419,Human_Splice_Rec_142430,Human_Splice_Rec_142431,Human_Splice_Rec_142440,Human_Splice_Rec_142441,Human_Splice_Rec_142448,Human_Splice_Rec_142449,Human_Splice_Rec_142458,Human_Splice_Rec_142459,Human_Splice_Rec_142472 Human_miRNA_ID_2170728,Human_miRNA_ID_2170729 RMVar_hsa_circ_136809,RMVar_hsa_circ_91850,RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_66101,RMVar_hsa_circ_136813,RMVar_hsa_circ_15909,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,RMVar_hsa_circ_361492,RMVar_hsa_circ_327572,RMVar_hsa_circ_63473,RMVar_hsa_circ_4850,RMVar_hsa_circ_71294,RMVar_hsa_circ_136817,RMVar_hsa_circ_136818,RMVar_hsa_circ_136819,RMVar_hsa_circ_98847,RMVar_hsa_circ_57307,RMVar_hsa_circ_353599,RMVar_hsa_circ_293454,RMVar_hsa_circ_136822,RMVar_hsa_circ_63269,RMVar_hsa_circ_357308,RMVar_hsa_circ_136821,RMVar_hsa_circ_292980,RMVar_hsa_circ_136827,RMVar_hsa_circ_279689,RMVar_hsa_circ_136824,RMVar_hsa_circ_297674,RMVar_hsa_circ_318796,RMVar_hsa_circ_104416,RMVar_hsa_circ_125478,RMVar_hsa_circ_136828,RMVar_hsa_circ_136829,RMVar_hsa_circ_136825,RMVar_hsa_circ_136826 94016 RMVar_ID_94016 Human_SNP_ID_34932172 m1A Human chr1 + 156333499 156333498 156333500 TGTAACAGAATTTCCTTCTTAAAATATGACACAGGTGTTACTTCTAATTTTTCCTTATCAACCTC TGTAACAGAATTTCCTTCTTAAAATATGACAC__GTGTTACTTCTAATTTTTCCTTATCAACCTC CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156333497..156333691 26863196 MeRIP-seq:(Medium) rs1192462253 Functional Loss DEL dbSNP153 33..34 33 - - - 94017 RMVar_ID_94017 Human_SNP_ID_34932173 m1A Human chr1 + 156333499 156333499 156333499 TGTAACAGAATTTCCTTCTTAAAATATGACACAGGTGTTACTTCTAATTTTTCCTTATCAACCTC TGTAACAGAATTTCCTTCTTAAAATATGACACGGGTGTTACTTCTAATTTTTCCTTATCAACCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156333497..156333691 26863196 MeRIP-seq:(Medium) rs1019812431 Functional Loss SNV dbSNP153 33..33 33 - - - 94018 RMVar_ID_94018 Human_SNP_ID_34932577 m1A Human chr1 + 156334913 156334913 156334913 TTGGGTCCCAAACATGTTCGGATGATATCTGCAATAGTCTAATGGAAAGGGAACATAAAATACGC TTGGGTCCCAAACATGTTCGGATGATATCTGCGATAGTCTAATGGAAAGGGAACATAAAATACGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156334659..156334973 26863196 MeRIP-seq:(Medium) rs1227415940 Functional Loss SNV dbSNP153 33..33 33 - - - 94019 RMVar_ID_94019 Human_SNP_ID_34933487 m1A Human chr1 + 156338208 156338208 156338208 GCCCATCATGGCGACGCGATGCAGAGCCGGGTACCCAGAGCTGGGGGAACCGGCAGAACCTTCTG GCCCATCATGGCGACGCGATGCAGAGCCGGGTCCCCAGAGCTGGGGGAACCGGCAGAACCTTCTG A C TSACC Ensembl:ENSG00000163467 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr1:156338130..156338275;chr1:156337784..156338275 26863410,32194978 MeRIP-seq:(Medium) rs753553271 Functional Loss SNV dbSNP153 33..33 33 - - - 94020 RMVar_ID_94020 Human_SNP_ID_34933521 m1A Human chr1 + 156338258 156338258 156338258 CGGCAGAACCTTCTGGAGAGAGAGAACCAGACAGAAGCCCAGAAAACGCTGCCTCCTCAGGGCTT CGGCAGAACCTTCTGGAGAGAGAGAACCAGACGGAAGCCCAGAAAACGCTGCCTCCTCAGGGCTT A G TSACC Ensembl:ENSG00000163467 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:156338226..156338300 26863196 MeRIP-seq:(Medium) rs978716093 Functional Loss SNV dbSNP153 33..33 33 - - - 94021 RMVar_ID_94021 Human_SNP_ID_34965638 m1A Human chr1 - 156466655 156466655 156466655 GAGAGTCGGCCTGGACTTCCCTGGGGTGCTCCAGGCCAGAGCTCTTTCATTGGGGCGAGTGTGGT GAGAGTCGGCCTGGACTTCCCTGGGGTGCTCCGGGCCAGAGCTCTTTCATTGGGGCGAGTGTGGT T C MEF2D Ensembl:ENSG00000116604 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156466607..156466717 26863196 MeRIP-seq:(Medium) rs912287777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9352395,Human_RBP_ID_17727415,Human_RBP_ID_26386536 Human_miRNA_ID_1090212,Human_miRNA_ID_1987508 RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 94022 RMVar_ID_94022 Human_SNP_ID_34965707 m1A Human chr1 + 156466907 156466906 156466908 GCTCTCTTGTCTTTCCCTCCAAATGTGCTTCCAGAGAGGCCCCCACCTCAAACCCCTGTCTCCAG GCTCTCTTGTCTTTCCCTCCAAATGTGCTTCC__AGAGGCCCCCACCTCAAACCCCTGTCTCCAG CAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156466474..156467126 32194978 MeRIP-seq:(Medium) rs1433293037 Functional Loss DEL dbSNP153 33..34 33 - - - 94023 RMVar_ID_94023 Human_SNP_ID_34965915 m1A Human chr1 + 156467626 156467622 156467627 GAGATTGTCAACTCTTCATCAGGGAGGCTGAGAGGAGGGGAGTGGGAATCGTCACTTTAATGTCT GAGATTGTCAACTCTTCATCAGGGAGGCT_____GAGGGGAGTGGGAATCGTCACTTTAATGTCT TGAGAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156467577..156467654 26863196 MeRIP-seq:(Medium) rs752818500 Functional Loss DEL dbSNP153 30..34 33 - - - 94024 RMVar_ID_94024 Human_SNP_ID_34965917 m1A Human chr1 + 156467626 156467626 156467626 GAGATTGTCAACTCTTCATCAGGGAGGCTGAGAGGAGGGGAGTGGGAATCGTCACTTTAATGTCT GAGATTGTCAACTCTTCATCAGGGAGGCTGAGTGGAGGGGAGTGGGAATCGTCACTTTAATGTCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156467577..156467654 26863196 MeRIP-seq:(Medium) rs1020757973 Functional Loss SNV dbSNP153 33..33 33 - - - 94025 RMVar_ID_94025 Human_SNP_ID_34966327 m1A Human chr1 - 156468831 156468831 156468831 GCCACAGCCACAGCAGCCTCAGCAGCCGCAACAGCCACCTCAGCAACAGTCCCACCTGGTCCCTG GCCACAGCCACAGCAGCCTCAGCAGCCGCAACGGCCACCTCAGCAACAGTCCCACCTGGTCCCTG T C MEF2D Ensembl:ENSG00000116604 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156468751..156468954;chr1:156468760..156468940 26863196 MeRIP-seq:(Medium) rs1279704801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17338485,Human_RBP_ID_18553401,Human_RBP_ID_19151700 Human_Splice_Rec_142859,Human_Splice_Rec_142881,Human_Splice_Rec_142901,Human_Splice_Rec_142917,Human_Splice_Rec_142933 RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 94026 RMVar_ID_94026 Human_SNP_ID_34969088 m1A Human chr1 - 156479700 156479686 156479701 TGCAGTTCAGCAATCCCAGCGGCTCCCTGGTCACCCCTTCCCTGGTGACATCATCCCTCACGGAC TGCAGTTCAGCAATCCCAGCGGCTCCCTGGT_______________GACATCATCCCTCACGGAC CACCAGGGAAGGGGTG C MEF2D Ensembl:ENSG00000116604 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156479649..156479773 26863196 MeRIP-seq:(Medium) rs751946964 Functional Loss DEL dbSNP153 32..46 33 - - - Human_Splice_Rec_142850,Human_Splice_Rec_142870,Human_Splice_Rec_142892 Human_miRNA_ID_2383601 RMVar_hsa_circ_22376,RMVar_hsa_circ_51128,RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846,RMVar_hsa_circ_343418,RMVar_hsa_circ_94677,RMVar_hsa_circ_136849 94027 RMVar_ID_94027 Human_SNP_ID_34971714 m1A Human chr1 - 156490077 156490077 156490077 GGTAATGCCCCCCACTTCTTTTGTGAAGGAAGAGCTCACTGTGTGAACCACAGAATGATCCTGGA GGTAATGCCCCCCACTTCTTTTGTGAAGGAAGGGCTCACTGTGTGAACCACAGAATGATCCTGGA T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156490075..156490257 26863196 MeRIP-seq:(Medium) rs1327748847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109353,RMVar_hsa_circ_112745,RMVar_hsa_circ_136853,RMVar_hsa_circ_136854 94028 RMVar_ID_94028 Human_SNP_ID_34971945 m1A Human chr1 - 156490903 156490903 156490903 GAGAGCCAAATGGCCTCACAGCTGCTACAGGAAGGATGAGAGCTAGACTACAGGAAGAACAAGCT GAGAGCCAAATGGCCTCACAGCTGCTACAGGACGGATGAGAGCTAGACTACAGGAAGAACAAGCT T G MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156490901..156491020 26863196 MeRIP-seq:(Medium) rs1472635876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109353,RMVar_hsa_circ_136854 94029 RMVar_ID_94029 Human_SNP_ID_34973323 m1A Human chr1 - 156496566 156496566 156496566 AGAACTTTGAAGAGAGAAGGGCTGACTGGAGCAGGAGGGATTAAGGTTAGACCACAGATGGGCAG AGAACTTTGAAGAGAGAAGGGCTGACTGGAGCGGGAGGGATTAAGGTTAGACCACAGATGGGCAG T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156496564..156496737 26863196 MeRIP-seq:(Medium) rs1426204551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5697160,Human_RBP_ID_10608040 RMVar_hsa_circ_109353,RMVar_hsa_circ_136854 94030 RMVar_ID_94030 Human_SNP_ID_34973649 m1A Human chr1 + 156497928 156497926 156497929 CACAGCAGAGGGACCCTCTGAGGGCACGGTAGAGGAGAAGGGTCTGAGGGGCTGGGCCATAATCA CACAGCAGAGGGACCCTCTGAGGGCACGGTA___GAGAAGGGTCTGAGGGGCTGGGCCATAATCA AGAG A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156497923..156498024 32194978 MeRIP-seq:(Medium) rs1418905613 Functional Loss DEL dbSNP153 32..34 33 - - - 94031 RMVar_ID_94031 Human_SNP_ID_34973810 m1A Human chr1 + 156498348 156498348 156498348 GGCATTGAGTACAGCAGACAGAAGCTCTAGCCAATTCCCCATGCCCATCCCCCAACACAAGGATC GGCATTGAGTACAGCAGACAGAAGCTCTAGCCCATTCCCCATGCCCATCCCCCAACACAAGGATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156498344..156498456 26863196 MeRIP-seq:(Medium) rs1318193962 Functional Loss SNV dbSNP153 33..33 33 - - - 94032 RMVar_ID_94032 Human_SNP_ID_34974522 m1A Human chr1 + 156500669 156500669 156500669 AGGCCTGGGCCCCCGTCGTGGGCGCGGGGGCCAGCAGGCGGGCGGCAGGCAAGCGGGGAACCGGG AGGCCTGGGCCCCCGTCGTGGGCGCGGGGGCCGGCAGGCGGGCGGCAGGCAAGCGGGGAACCGGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:156500576..156500790 26863410 MeRIP-seq:(Medium) rs1467709137 Functional Loss SNV dbSNP153 33..33 33 - - - 94033 RMVar_ID_94033 Human_SNP_ID_34975950 m1A Human chr1 - 156505589 156505589 156505589 GCTCTACCCTGCATTCCTTTCTGCTCCAAGACATTTCCCCACATCCCATTTCGTTCCTCCCAAGC GCTCTACCCTGCATTCCTTTCTGCTCCAAGACTTTTCCCCACATCCCATTTCGTTCCTCCCAAGC T A lnc-MEF2D-1 RNACentral:URS00008BD488 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156505572..156505643 26863196 MeRIP-seq:(Medium) rs1272602887 Functional Loss SNV dbSNP153 33..33 33 - - - 94034 RMVar_ID_94034 Human_SNP_ID_34980651 m1A Human chr1 - 156526075 156526075 156526075 CCTTCTCTCTGCACTCCCACAAAGCCAGGGCCAGGCTCCCCATCCCTACCTCCCACTGCATCAGC CCTTCTCTCTGCACTCCCACAAAGCCAGGGCCGGGCTCCCCATCCCTACCTCCCACTGCATCAGC T C IQGAP3 Ensembl:ENSG00000183856 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156526025..156526155 26863196 MeRIP-seq:(Medium) rs888819847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109263,Human_RBP_ID_5312726,Human_RBP_ID_18930110 RMVar_hsa_circ_98213,RMVar_hsa_circ_104223,RMVar_hsa_circ_136856,RMVar_hsa_circ_87136,RMVar_hsa_circ_136857,RMVar_hsa_circ_136855 94035 RMVar_ID_94035 Human_SNP_ID_34981330 m1A Human chr1 - 156528245 156528245 156528245 GGTGAGAACAGCTGCGTAGGGCGGGGCAGATAAAGAGATGGTGTGGGGAGCAGAAGTAAAATGGA GGTGAGAACAGCTGCGTAGGGCGGGGCAGATATAGAGATGGTGTGGGGAGCAGAAGTAAAATGGA T A IQGAP3 Ensembl:ENSG00000183856 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:156528147..156528415;chr1:156528177..156528379;chr1:156528143..156528356 26863196 MeRIP-seq:(Medium) rs934849523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23336641 RMVar_hsa_circ_98213,RMVar_hsa_circ_104223,RMVar_hsa_circ_136856,RMVar_hsa_circ_87136,RMVar_hsa_circ_136857,RMVar_hsa_circ_136855 94036 RMVar_ID_94036 Human_SNP_ID_34983052 m1A Human chr1 + 156534227 156534227 156534227 CTTCTGTCCCCATCATTTCCCCAGCCTTCTCCAGTGATTGCTCAGGCCAATTTGGACTCTCCAGT CTTCTGTCCCCATCATTTCCCCAGCCTTCTCCGGTGATTGCTCAGGCCAATTTGGACTCTCCAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156534177..156534365 26863196 MeRIP-seq:(Medium) rs1377436173 Functional Loss SNV dbSNP153 33..33 33 - - - 94037 RMVar_ID_94037 Human_SNP_ID_34988495 m1A Human chr1 + 156556693 156556693 156556693 TGGCTTTGTTGATCCGCTGCACAGCGTGGAGCACTGCAAGGCAGGAGAGCAACAGGTTGTACTGG TGGCTTTGTTGATCCGCTGCACAGCGTGGAGCCCTGCAAGGCAGGAGAGCAACAGGTTGTACTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156556677..156556745 26863196 MeRIP-seq:(Medium) rs746235312 Functional Loss SNV dbSNP153 33..33 33 - - - 94038 RMVar_ID_94038 Human_SNP_ID_34990061 m1A Human chr1 + 156562183 156562183 156562183 AAATTCTTCAGCTTGGTCTTCACAGCCTTCTCACTTCGCCGCCCCAGACCCCAAGGATATCCTCA AAATTCTTCAGCTTGGTCTTCACAGCCTTCTCGCTTCGCCGCCCCAGACCCCAAGGATATCCTCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156562022..156562387 26863196 MeRIP-seq:(Medium) rs1218576884 Functional Loss SNV dbSNP153 33..33 33 - - - 94039 RMVar_ID_94039 Human_SNP_ID_34990150 m1A Human chr1 - 156562552 156562552 156562552 AAGAGACCTCGAGCAGGAGTGGTTTGGGGGTGACCTCAGGGTAAGCCCCTGCACTGGGAGGTTTG AAGAGACCTCGAGCAGGAGTGGTTTGGGGGTGCCCTCAGGGTAAGCCCCTGCACTGGGAGGTTTG T G IQGAP3 Ensembl:ENSG00000183856 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7548309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850519,Human_RBP_ID_19039495,Human_RBP_ID_22351944 GWAS_ID_12222,GWAS_ID_12223,GWAS_ID_12224,GWAS_ID_12225,GWAS_ID_12226,GWAS_ID_12227,GWAS_ID_12228,GWAS_ID_12229,GWAS_ID_12230,GWAS_ID_12231,GWAS_ID_12232,GWAS_ID_12233,GWAS_ID_12234,GWAS_ID_12235,GWAS_ID_12236,GWAS_ID_12237,GWAS_ID_12238,GWAS_ID_12239,GWAS_ID_12240 RMVar_hsa_circ_5204,RMVar_hsa_circ_98213,RMVar_hsa_circ_136857,RMVar_hsa_circ_105275,RMVar_hsa_circ_136863,RMVar_hsa_circ_80838,RMVar_hsa_circ_136864,RMVar_hsa_circ_92144,RMVar_hsa_circ_128164,RMVar_hsa_circ_136867,RMVar_hsa_circ_38439,RMVar_hsa_circ_126915,RMVar_hsa_circ_136869,RMVar_hsa_circ_111007,RMVar_hsa_circ_136871,RMVar_hsa_circ_136872,RMVar_hsa_circ_120953,RMVar_hsa_circ_19393,RMVar_hsa_circ_96156,RMVar_hsa_circ_136874,RMVar_hsa_circ_136875,RMVar_hsa_circ_370622,RMVar_hsa_circ_136876 94040 RMVar_ID_94040 Human_SNP_ID_34991931 m1A Human chr1 + 156569462 156569462 156569462 TGCTCATCCATCTCCTCAGCTGTGAGGCGTTCATCTGAGGAGTTAAACGGGATAAGGTCAATGAA TGCTCATCCATCTCCTCAGCTGTGAGGCGTTCCTCTGAGGAGTTAAACGGGATAAGGTCAATGAA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156569309..156569512 26863196 MeRIP-seq:(Medium) rs781164390 Functional Loss SNV dbSNP153 33..33 33 - - - 94041 RMVar_ID_94041 Human_SNP_ID_34992096 m1A Human chr1 - 156569833 156569833 156569833 CTCTGAGCAGGGTTGCCTAAACAAGTCTGTTGAGAAGATGTTTCGGCTGGGCATGGTGGCGGCTC CTCTGAGCAGGGTTGCCTAAACAAGTCTGTTGGGAAGATGTTTCGGCTGGGCATGGTGGCGGCTC T C IQGAP3 Ensembl:ENSG00000183856 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156569830..156569949 26863196 MeRIP-seq:(Medium) rs994164381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128164,RMVar_hsa_circ_136869 94042 RMVar_ID_94042 Human_SNP_ID_34992584 m1A Human chr1 + 156572285 156572285 156572285 AGGAAGAAAGTTCTTTGTAAGCTTTAAAGCGCAGCACATTAGTCAGGGGACAATGCGCCGCTCAC AGGAAGAAAGTTCTTTGTAAGCTTTAAAGCGCCGCACATTAGTCAGGGGACAATGCGCCGCTCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156572282..156572575 26863196 MeRIP-seq:(Medium) rs1557950925 Functional Loss SNV dbSNP153 33..33 33 - - - 94043 RMVar_ID_94043 Human_SNP_ID_34992623 m1A Human chr1 + 156572437 156572437 156572437 GACACACGCCCCAATCTCTCCCGGGACAGCCAAGCCCCCGACCAGCGGCACCACTGCGAGACCCT GACACACGCCCCAATCTCTCCCGGGACAGCCACGCCCCCGACCAGCGGCACCACTGCGAGACCCT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:156572403..156572519 26863196 MeRIP-seq:(Medium) rs1271410537 Functional Loss SNV dbSNP153 33..33 33 - - - 94044 RMVar_ID_94044 Human_SNP_ID_34992659 m1A Human chr1 - 156572515 156572515 156572515 CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCAGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCTGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG T A IQGAP3 Ensembl:ENSG00000183856 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156566376..156572586;chr1:156566395..156572575 26863196 MeRIP-seq:(Medium) rs140461633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222985,Human_RBP_ID_18415655,Human_RBP_ID_18969179,Human_RBP_ID_22637656,Human_RBP_ID_24541229,Human_RBP_ID_26312017,Human_RBP_ID_27798663 Human_Splice_Rec_142945,Human_Splice_Rec_143017 RMVar_hsa_circ_128164,RMVar_hsa_circ_136869 94045 RMVar_ID_94045 Human_SNP_ID_34992660 m1A Human chr1 - 156572515 156572515 156572515 CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCAGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCCGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG T G IQGAP3 Ensembl:ENSG00000183856 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156566376..156572586;chr1:156566395..156572575 26863196 MeRIP-seq:(Medium) rs140461633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222985,Human_RBP_ID_18415655,Human_RBP_ID_18969179,Human_RBP_ID_22637656,Human_RBP_ID_24541229,Human_RBP_ID_26312017,Human_RBP_ID_27798663 Human_Splice_Rec_142945,Human_Splice_Rec_143017 RMVar_hsa_circ_128164,RMVar_hsa_circ_136869 94046 RMVar_ID_94046 Human_SNP_ID_34998148 m1A Human chr1 - 156591860 156591860 156591860 GACAGGCGATGGTCTGGCTTTTGATCCGCGGCACGCGCGAGCCCGCAACCAGCAGCCCGAGGCCC GACAGGCGATGGTCTGGCTTTTGATCCGCGGCTCGCGCGAGCCCGCAACCAGCAGCCCGAGGCCC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156591751..156592000;chr1:156591812..156591928 26863410,26863196 MeRIP-seq:(Medium) rs1269457222 Functional Loss SNV dbSNP153 33..33 33 - - - 94047 RMVar_ID_94047 Human_SNP_ID_34998158 m1A Human chr1 + 156591878 156591878 156591878 TGCGGGCTCGCGCGTGCCGCGGATCAAAAGCCAGACCATCGCCTGTCGCTCGGGACCCACCTGGT TGCGGGCTCGCGCGTGCCGCGGATCAAAAGCCGGACCATCGCCTGTCGCTCGGGACCCACCTGGT A G NAXE Ensembl:ENSG00000163382 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156591776..156591920 26863196 MeRIP-seq:(Medium) rs1186285446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073097,Human_RBP_ID_5108811,Human_RBP_ID_5311872,Human_RBP_ID_5456438,Human_RBP_ID_9319208,Human_RBP_ID_22428645,Human_RBP_ID_26843938 RMVar_hsa_circ_117354,RMVar_hsa_circ_136880 94048 RMVar_ID_94048 Human_SNP_ID_34998264 m1A Human chr1 + 156592134 156592134 156592134 CAGGAGGAGGCCCAGGCCGTGGACCAGGAGCTATTTAACGAATACCAGTTCAGCGTGGACCAACT CAGGAGGAGGCCCAGGCCGTGGACCAGGAGCTTTTTAACGAATACCAGTTCAGCGTGGACCAACT A T NAXE Ensembl:ENSG00000163382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156592101..156592706 32194978 MeRIP-seq:(Medium) rs753746153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22783,Human_RBP_ID_1413446,Human_RBP_ID_1727006,Human_RBP_ID_4082802,Human_RBP_ID_5433031,Human_RBP_ID_19202226,Human_RBP_ID_26843940,Human_RBP_ID_27169648 Human_Splice_Rec_143138,Human_Splice_Rec_143139,Human_Splice_Rec_143148,Human_Splice_Rec_143149,Human_Splice_Rec_143158,Human_Splice_Rec_143159,Human_Splice_Rec_143166,Human_Splice_Rec_143167 Human_miRNA_ID_2919908 RMVar_hsa_circ_117354,RMVar_hsa_circ_136880 94049 RMVar_ID_94049 Human_SNP_ID_34998331 m1A Human chr1 + 156592332 156592332 156592332 AGCTGGGCCAATATGGTCTATTACCGCCTGAAACCCCGCCGAACCACCCTTGACTCTGCCTTCAG AGCTGGGCCAATATGGTCTATTACCGCCTGAACCCCCGCCGAACCACCCTTGACTCTGCCTTCAG A C NAXE Ensembl:ENSG00000163382 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156592330..156592576 26863196 MeRIP-seq:(Medium) rs1025418049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5338617,Human_RBP_ID_22469497 RMVar_hsa_circ_117354,RMVar_hsa_circ_136880 94050 RMVar_ID_94050 Human_SNP_ID_34998884 m1A Human chr1 - 156593990 156593990 156593990 TCTCCAGAGCAGGTGGCACAAAACGACCCCCCAGGTAATGGTAGCGACCGGTAAACTGGGTTGCA TCTCCAGAGCAGGTGGCACAAAACGACCCCCCCGGTAATGGTAGCGACCGGTAAACTGGGTTGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156593939..156594062 26863196 MeRIP-seq:(Medium) rs1557963525 Functional Loss SNV dbSNP153 33..33 33 - - - 94051 RMVar_ID_94051 Human_SNP_ID_34998890 m1A Human chr1 - 156594002 156594002 156594002 GCTGGTACTTCTTCTCCAGAGCAGGTGGCACAAAACGACCCCCCAGGTAATGGTAGCGACCGGTA GCTGGTACTTCTTCTCCAGAGCAGGTGGCACAGAACGACCCCCCAGGTAATGGTAGCGACCGGTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156593951..156594125 32194978 MeRIP-seq:(Medium) rs1245765243 Functional Loss SNV dbSNP153 33..33 33 - - - 94052 RMVar_ID_94052 Human_SNP_ID_34999213 m1A Human chr1 - 156595184 156595183 156595184 GTGATGGAAGAAGCAGGAAAAGCAAGAAGAAAAGACAGCAGCATCAAGAGGAGGAGGACATCTTG GTGATGGAAGAAGCAGGAAAAGCAAGAAGAAA_GACAGCAGCATCAAGAGGAGGAGGACATCTTG CT C GPATCH4 Ensembl:ENSG00000160818 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156595151..156595225 26863196 MeRIP-seq:(Medium) rs769661827 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2097079,Human_RBP_ID_5697326,Human_RBP_ID_24541521,Human_RBP_ID_26314837 94053 RMVar_ID_94053 Human_SNP_ID_35000074 m1A Human chr1 - 156598116 156598116 156598116 TTCACTGGTACTGATAATTCTCTACAGGATGGAGTACAGATAAGGAGCCTTTCTAAGGAGACCAC TTCACTGGTACTGATAATTCTCTACAGGATGGGGTACAGATAAGGAGCCTTTCTAAGGAGACCAC T C GPATCH4 Ensembl:ENSG00000160818 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156598114..156598241 26863196 MeRIP-seq:(Medium) rs1404340272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413487,Human_RBP_ID_10608859 Human_Splice_Rec_143180,Human_Splice_Rec_143181,Human_Splice_Rec_143194,Human_Splice_Rec_143195,Human_Splice_Rec_143213,Human_Splice_Rec_143222,Human_Splice_Rec_143223,Human_Splice_Rec_143236,Human_Splice_Rec_143237,Human_Splice_Rec_143254,Human_Splice_Rec_143262,Human_Splice_Rec_143263,Human_Splice_Rec_143274,Human_Splice_Rec_143275,Human_Splice_Rec_143288,Human_Splice_Rec_143289,Human_Splice_Rec_143298 RMVar_hsa_circ_8121 94054 RMVar_ID_94054 Human_SNP_ID_35000128 m1A Human chr1 - 156598273 156598273 156598273 TGCCAAGGAGTTCACAAACCACTGGTGGAATGAGCTCTTCAACAAGACTGCGGCCAACTTGGTAG TGCCAAGGAGTTCACAAACCACTGGTGGAATGGGCTCTTCAACAAGACTGCGGCCAACTTGGTAG T C GPATCH4 Ensembl:ENSG00000160818 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156598125..156598476 32194978 MeRIP-seq:(Medium) rs761122138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413490,Human_RBP_ID_1727029,Human_RBP_ID_10608863,Human_RBP_ID_17446684,Human_RBP_ID_23336771 Human_Splice_Rec_143178,Human_Splice_Rec_143179,Human_Splice_Rec_143192,Human_Splice_Rec_143193,Human_Splice_Rec_143206,Human_Splice_Rec_143207,Human_Splice_Rec_143220,Human_Splice_Rec_143221,Human_Splice_Rec_143234,Human_Splice_Rec_143235,Human_Splice_Rec_143252,Human_Splice_Rec_143253,Human_Splice_Rec_143260,Human_Splice_Rec_143261,Human_Splice_Rec_143272,Human_Splice_Rec_143273,Human_Splice_Rec_143286,Human_Splice_Rec_143287,Human_Splice_Rec_143296,Human_Splice_Rec_143297,Human_Splice_Rec_143302,Human_Splice_Rec_143308 RMVar_hsa_circ_8121 94055 RMVar_ID_94055 Human_SNP_ID_35000904 m1A Human chr1 + 156601438 156601437 156601439 TACCGTCATTGCTGGGTCCGCTCCGCGGAAACATGTGCCGGACCTGACTTGTGCGCCGCCATCTT TACCGTCATTGCTGGGTCCGCTCCGCGGAAAC__GTGCCGGACCTGACTTGTGCGCCGCCATCTT CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156601347..156601475;chr1:156601335..156601475 26863196 MeRIP-seq:(Medium) rs1364839460 Functional Loss DEL dbSNP153 33..34 33 - - - 94056 RMVar_ID_94056 Human_SNP_ID_35000905 m1A Human chr1 + 156601438 156601438 156601438 TACCGTCATTGCTGGGTCCGCTCCGCGGAAACATGTGCCGGACCTGACTTGTGCGCCGCCATCTT TACCGTCATTGCTGGGTCCGCTCCGCGGAAACCTGTGCCGGACCTGACTTGTGCGCCGCCATCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156601347..156601475;chr1:156601335..156601475 26863196 MeRIP-seq:(Medium) rs553801671 Functional Loss SNV dbSNP153 33..33 33 - - - 94057 RMVar_ID_94057 Human_SNP_ID_35000906 m1A Human chr1 + 156601438 156601438 156601438 TACCGTCATTGCTGGGTCCGCTCCGCGGAAACATGTGCCGGACCTGACTTGTGCGCCGCCATCTT TACCGTCATTGCTGGGTCCGCTCCGCGGAAACTTGTGCCGGACCTGACTTGTGCGCCGCCATCTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156601347..156601475;chr1:156601335..156601475 26863196 MeRIP-seq:(Medium) rs553801671 Functional Loss SNV dbSNP153 33..33 33 - - - 94058 RMVar_ID_94058 Human_SNP_ID_35006800 m1A Human chr1 - 156625265 156625265 156625265 CCCGCAGCGCGGCCTCGGCGTGGTGATTGGGAAGCGCACACTGCCGTCAGCCAGCCAGCCGCCGT CCCGCAGCGCGGCCTCGGCGTGGTGATTGGGAGGCGCACACTGCCGTCAGCCAGCCAGCCGCCGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:156625176..156625277 26863410 MeRIP-seq:(Medium) rs1003041645 Functional Loss SNV dbSNP153 33..33 33 - - - 94059 RMVar_ID_94059 Human_SNP_ID_35011631 m1A Human chr1 - 156643841 156643841 156643841 AGAGCTCAGCAGTCATGCGGTCCGTTCCCTTGACGCCACAACATCCCCCTCTCTGTTTCAGCTCC AGAGCTCAGCAGTCATGCGGTCCGTTCCCTTGGCGCCACAACATCCCCCTCTCTGTTTCAGCTCC T C AL365181.3 Ensembl:ENSG00000272405 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156643741..156643927 26863196 MeRIP-seq:(Medium) rs1236574196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3188202,Human_miRNA_ID_3194220 94060 RMVar_ID_94060 Human_SNP_ID_35012328 m1A Human chr1 - 156646600 156646600 156646600 AGGTCCTCCAGGACCACCCCGACGGTCTCCAGACCCATCCCCCAAAGTCTCCCAGTCAATTCAGC AGGTCCTCCAGGACCACCCCGACGGTCTCCAGTCCCATCCCCCAAAGTCTCCCAGTCAATTCAGC T A AL590666.2 Ensembl:ENSG00000229953 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156646551..156646815 26863196 MeRIP-seq:(Medium) rs1369902881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8244047,Human_RBP_ID_17072499,Human_RBP_ID_18930115 Human_miRNA_ID_3188203,Human_miRNA_ID_3194221,Human_miRNA_ID_3196347 94061 RMVar_ID_94061 Human_SNP_ID_35012329 m1A Human chr1 - 156646600 156646600 156646600 AGGTCCTCCAGGACCACCCCGACGGTCTCCAGACCCATCCCCCAAAGTCTCCCAGTCAATTCAGC AGGTCCTCCAGGACCACCCCGACGGTCTCCAGGCCCATCCCCCAAAGTCTCCCAGTCAATTCAGC T C AL590666.2 Ensembl:ENSG00000229953 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156646551..156646815 26863196 MeRIP-seq:(Medium) rs1369902881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8244047,Human_RBP_ID_17072499,Human_RBP_ID_18930115 Human_miRNA_ID_3188203,Human_miRNA_ID_3194221,Human_miRNA_ID_3196347 94062 RMVar_ID_94062 Human_SNP_ID_35012346 m1A Human chr1 - 156646661 156646647 156646661 CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCCAGGGGCCAGGGTCCTGCAGCCCTACCTCTAGGT CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCC______________TGCAGCCCTACCTCTAGGT AGGACCCTGGCCCCT A AL590666.2 Ensembl:ENSG00000229953 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156646551..156646700 26863196 MeRIP-seq:(Medium) rs1211135066 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_4076068,Human_RBP_ID_26774607 Human_miRNA_ID_3149867,Human_miRNA_ID_3175580 94063 RMVar_ID_94063 Human_SNP_ID_35012362 m1A Human chr1 - 156646661 156646655 156646661 CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCCAGGGGCCAGGGTCCTGCAGCCCTACCTCTAGGT CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCC______CAGGGTCCTGCAGCCCTACCTCTAGGT GGCCCCT G AL590666.2 Ensembl:ENSG00000229953 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156646551..156646700 26863196 MeRIP-seq:(Medium) rs767167576 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4076068,Human_RBP_ID_26774607 Human_miRNA_ID_3149867,Human_miRNA_ID_3175580 94064 RMVar_ID_94064 Human_SNP_ID_35012369 m1A Human chr1 - 156646661 156646661 156646661 CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCCAGGGGCCAGGGTCCTGCAGCCCTACCTCTAGGT CCCGGCCCCCCTAGGACCAGGGGCCAGGGGCCGGGGGCCAGGGTCCTGCAGCCCTACCTCTAGGT T C AL590666.2 Ensembl:ENSG00000229953 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156646551..156646700 26863196 MeRIP-seq:(Medium) rs976901538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4076068,Human_RBP_ID_26774607 Human_miRNA_ID_3149867,Human_miRNA_ID_3175580 94065 RMVar_ID_94065 Human_SNP_ID_35014354 m1A Human chr1 - 156653016 156653016 156653016 AGACCCATAGGTAGAGGTGGGTAAGAGAATGAAGGCAAAGGACAGGAGAGTTTGGGATGATGGTG AGACCCATAGGTAGAGGTGGGTAAGAGAATGATGGCAAAGGACAGGAGAGTTTGGGATGATGGTG T A AL590666.2 Ensembl:ENSG00000229953 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156653014..156653260 26863196 MeRIP-seq:(Medium) rs1295149003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5540956 94066 RMVar_ID_94066 Human_SNP_ID_35014492 m1A Human chr1 - 156653487 156653487 156653487 AATGAGAGAGGTGGACAGCAGGAGATGGAGACAGAGGGTACCAGAGCTTGGTTACAAAGCGGTTT AATGAGAGAGGTGGACAGCAGGAGATGGAGACCGAGGGTACCAGAGCTTGGTTACAAAGCGGTTT T G AL590666.2 Ensembl:ENSG00000229953 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156653484..156653699 26863196 MeRIP-seq:(Medium) rs1423729543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5540959 94067 RMVar_ID_94067 Human_SNP_ID_35015421 m1A Human chr1 + 156657111 156657111 156657111 AACAGGACTTCATCAACAGTGGGCTGGGAGACAGGGCGGGAGGGGCCCCTGCCATATGCTCTCAC AACAGGACTTCATCAACAGTGGGCTGGGAGACGGGGCGGGAGGGGCCCCTGCCATATGCTCTCAC A G BCAN Ensembl:ENSG00000132692 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156657109..156657256 26863196 MeRIP-seq:(Medium) rs768899151 Functional Loss SNV dbSNP153 33..33 33 - - - 94068 RMVar_ID_94068 Human_SNP_ID_35015632 m1A Human chr1 - 156657720 156657720 156657720 GGACGCCATCCGACCACAAGAAGTCGCCTTCGATGGTCCTGTCGTTGAGTCCGATCCACTGGTAC GGACGCCATCCGACCACAAGAAGTCGCCTTCGGTGGTCCTGTCGTTGAGTCCGATCCACTGGTAC T C AL590666.2 Ensembl:ENSG00000229953 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156657718..156658103 26863196 MeRIP-seq:(Medium) rs1200538652 Functional Loss SNV dbSNP153 33..33 33 - - - 94069 RMVar_ID_94069 Human_SNP_ID_35016661 m1A Human chr1 - 156661270 156661270 156661270 TGATGGGAAACCAAAGCCCCTTCCAGCTCACCACCATGGGCTCTCTGGGGAATCCAATATACTAT TGATGGGAAACCAAAGCCCCTTCCAGCTCACCGCCATGGGCTCTCTGGGGAATCCAATATACTAT T C AL590666.2 Ensembl:ENSG00000229953 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156661262..156661401 26863196 MeRIP-seq:(Medium) rs1478597028 Functional Loss SNV dbSNP153 33..33 33 - - - 94070 RMVar_ID_94070 Human_SNP_ID_35018596 m1A Human chr1 - 156669054 156669054 156669054 TCCATCTCATAGGCTAAGTCAGCTGAATCCCGATAGTACTAGGTCCCCTTCCCTCCGCATCCCGT TCCATCTCATAGGCTAAGTCAGCTGAATCCCGGTAGTACTAGGTCCCCTTCCCTCCGCATCCCGT T C NES Ensembl:ENSG00000132688 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156669007..156669102 26863196 MeRIP-seq:(Medium) rs752999187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_156176,Human_miRNA_ID_2383603 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94071 RMVar_ID_94071 Human_SNP_ID_35018699 m1A Human chr1 - 156669312 156669312 156669312 CCTGGTCCTCAGGGGAGGACTAGGAAAAGACCATCTGCCCGGCACTGGGGACTTAGGGGTGCGGG CCTGGTCCTCAGGGGAGGACTAGGAAAAGACCGTCTGCCCGGCACTGGGGACTTAGGGGTGCGGG T C NES Ensembl:ENSG00000132688 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156669308..156669373 26863196 MeRIP-seq:(Medium) rs150109340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2256099,Human_miRNA_ID_2515632 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94072 RMVar_ID_94072 Human_SNP_ID_35018785 m1A Human chr1 - 156669532 156669532 156669532 TTGGAGGGGAAGTCACAGCATGTGAATGGGGGAGTGATGAACGGGCTGGAGCAGTCTGAGGAAGT TTGGAGGGGAAGTCACAGCATGTGAATGGGGGCGTGATGAACGGGCTGGAGCAGTCTGAGGAAGT T G NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156669484..156669639 26863196 MeRIP-seq:(Medium) rs145578225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8170759 Human_miRNA_ID_2972196,Human_miRNA_ID_3005378 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94073 RMVar_ID_94073 Human_SNP_ID_35018977 m1A Human chr1 - 156670013 156670013 156670013 GGTCCCTGGGGAGGTGGCAGAACCTCTGGGCCAGGTGCCCCAGCTGCTACTGGATCCTGCAGCCT GGTCCCTGGGGAGGTGGCAGAACCTCTGGGCCGGGTGCCCCAGCTGCTACTGGATCCTGCAGCCT T C NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156669821..156670106 26863196 MeRIP-seq:(Medium) rs1342318388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2649002,Human_miRNA_ID_2650949,Human_miRNA_ID_2682906 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94074 RMVar_ID_94074 Human_SNP_ID_35019511 m1A Human chr1 - 156671328 156671328 156671328 CGCAGTCTGCAGATGTGCAGAGGTGGGAAGATACGGTGGAGAAGGACCAAGAACTGGCTCAGGAA CGCAGTCTGCAGATGTGCAGAGGTGGGAAGATGCGGTGGAGAAGGACCAAGAACTGGCTCAGGAA T C NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156670647..156671500;chr1:156669796..156671505 26863196 MeRIP-seq:(Medium) rs375001753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22871863,Human_RBP_ID_23117574 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94075 RMVar_ID_94075 Human_SNP_ID_35020118 m1A Human chr1 - 156673020 156673020 156673020 AGGCCCGTACCCCTACCTTGGCCAGCACCCCCATCCCCCCCACACCTCAGGCACCCTCTCCTGCT AGGCCCGTACCCCTACCTTGGCCAGCACCCCCGTCCCCCCCACACCTCAGGCACCCTCTCCTGCT T C NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156673018..156673172 26863196 MeRIP-seq:(Medium) rs772195958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803587 Human_miRNA_ID_2652858,Human_miRNA_ID_2754053 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94076 RMVar_ID_94076 Human_SNP_ID_35020119 m1A Human chr1 - 156673020 156673020 156673020 AGGCCCGTACCCCTACCTTGGCCAGCACCCCCATCCCCCCCACACCTCAGGCACCCTCTCCTGCT AGGCCCGTACCCCTACCTTGGCCAGCACCCCCCTCCCCCCCACACCTCAGGCACCCTCTCCTGCT T G NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156673018..156673172 26863196 MeRIP-seq:(Medium) rs772195958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803587 Human_miRNA_ID_2652858,Human_miRNA_ID_2754053 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 94077 RMVar_ID_94077 Human_SNP_ID_35031028 m1A Human chr1 - 156714825 156714824 156714826 CTGCGCAGATGCAGCAAAGGAGGAGAAGACACAATGAGCACATGGCATGAGCCTTAAAGAATTTG CTGCGCAGATGCAGCAAAGGAGGAGAAGACA__ATGAGCACATGGCATGAGCCTTAAAGAATTTG TTG T lnc-ISG20L2-1 RNACentral:URS0000D5CED2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156714823..156715032 26863196 MeRIP-seq:(Medium) rs1414032355 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10609137 94078 RMVar_ID_94078 Human_SNP_ID_35031030 m1A Human chr1 + 156714848 156714848 156714848 TGTGCTCATTGTGTCTTCTCCTCCTTTGCTGCATCTGCGCAGCTCAGGTCACTGCATGTCTAGCT TGTGCTCATTGTGTCTTCTCCTCCTTTGCTGCGTCTGCGCAGCTCAGGTCACTGCATGTCTAGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156714811..156715022 26863196 MeRIP-seq:(Medium) rs1010806181 Functional Loss SNV dbSNP153 33..33 33 - - - 94079 RMVar_ID_94079 Human_SNP_ID_35031140 m1A Human chr1 - 156715421 156715421 156715421 AGACAGGAGGGATCCCAAGCTTAGCCTTGGCCAGCAGTAAGGACACCTTATCTTCTGGGAAAGAA AGACAGGAGGGATCCCAAGCTTAGCCTTGGCCGGCAGTAAGGACACCTTATCTTCTGGGAAAGAA T C lnc-ISG20L2-1 RNACentral:URS0000D5CED2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156715418..156715941 26863196 MeRIP-seq:(Medium) rs1173142220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10609158 94080 RMVar_ID_94080 Human_SNP_ID_35031220 m1A Human chr1 - 156715827 156715825 156715827 GGACTTACAAGCTTCTGGAGGTAGAGAGGCCTAAGAGAGAGCTACAAGACAGGTAAGAGGACAAT GGACTTACAAGCTTCTGGAGGTAGAGAGGCCT__GAGAGAGCTACAAGACAGGTAAGAGGACAAT CTT C lnc-ISG20L2-1 RNACentral:URS0000D5CED2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156715540..156715943 26863196 MeRIP-seq:(Medium) rs937735084 Functional Loss DEL dbSNP153 33..34 33 - - - 94081 RMVar_ID_94081 Human_SNP_ID_35031221 m1A Human chr1 - 156715827 156715827 156715827 GGACTTACAAGCTTCTGGAGGTAGAGAGGCCTAAGAGAGAGCTACAAGACAGGTAAGAGGACAAT GGACTTACAAGCTTCTGGAGGTAGAGAGGCCTCAGAGAGAGCTACAAGACAGGTAAGAGGACAAT T G lnc-ISG20L2-1 RNACentral:URS0000D5CED2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156715540..156715943 26863196 MeRIP-seq:(Medium) rs1307301970 Functional Loss SNV dbSNP153 33..33 33 - - - 94082 RMVar_ID_94082 Human_SNP_ID_35031309 m1A Human chr1 - 156716220 156716220 156716220 ATATAAAGAAGACCAGCAGGTTGGCCTGGTGCAGTAGCTTACACCTGTAATCCCAGCACTTTGGG ATATAAAGAAGACCAGCAGGTTGGCCTGGTGCTGTAGCTTACACCTGTAATCCCAGCACTTTGGG T A lnc-ISG20L2-1 RNACentral:URS0000D5CED2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156716218..156716357 26863196 MeRIP-seq:(Medium) rs1467321623 Functional Loss SNV dbSNP153 33..33 33 - - - 94083 RMVar_ID_94083 Human_SNP_ID_35034170 m1A Human chr1 - 156727238 156727238 156727238 AGATCAATAGCCACCCAACCCGCTCTCAGAAGAAGAGCTCCCAGAAGAAATCCTCTAAAAAGAAC AGATCAATAGCCACCCAACCCGCTCTCAGAAGGAGAGCTCCCAGAAGAAATCCTCTAAAAAGAAC T C ISG20L2 Ensembl:ENSG00000143319 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156727187..156727283 26863196 MeRIP-seq:(Medium) rs146047012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1727062,Human_RBP_ID_5519237,Human_RBP_ID_18522648 Human_miRNA_ID_2377245,Human_miRNA_ID_3092321 RMVar_hsa_circ_89340,RMVar_hsa_circ_136889 94084 RMVar_ID_94084 Human_SNP_ID_35034588 m1A Human chr1 - 156728627 156728612 156728627 GGGGCCGGGGAGCGCATCCCGCCCCCGCCCCCACCCACGCCGCCCCCTCCTCCGCCGCCACTGCC GGGGCCGGGGAGCGCATCCCGCCCCCGCCCCC_______________TCCTCCGCCGCCACTGCC AGGGGGCGGCGTGGGT A ISG20L2 Ensembl:ENSG00000143319 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:156728540..156728689 26863410 MeRIP-seq:(Medium) rs901936450 Functional Loss DEL dbSNP153 33..47 33 - - - 94085 RMVar_ID_94085 Human_SNP_ID_35034598 m1A Human chr1 - 156728627 156728627 156728627 GGGGCCGGGGAGCGCATCCCGCCCCCGCCCCCACCCACGCCGCCCCCTCCTCCGCCGCCACTGCC GGGGCCGGGGAGCGCATCCCGCCCCCGCCCCCCCCCACGCCGCCCCCTCCTCCGCCGCCACTGCC T G ISG20L2 Ensembl:ENSG00000143319 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:156728540..156728689 26863410 MeRIP-seq:(Medium) rs1388725532 Functional Loss SNV dbSNP153 33..33 33 - - - 94086 RMVar_ID_94086 Human_SNP_ID_35037463 m1A Human chr1 - 156738103 156738103 156738103 GCATTACCGCTACATTGGCAAGACCATGGATTACCGGGGAACCATGATCCCTAGTGAAGCCCCCT GCATTACCGCTACATTGGCAAGACCATGGATTTCCGGGGAACCATGATCCCTAGTGAAGCCCCCT T A MRPL24 Ensembl:ENSG00000143314 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156738026..156738150 26863196 MeRIP-seq:(Medium) rs1484378764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329027,Human_RBP_ID_743147,Human_RBP_ID_4000124 Human_Splice_Rec_143570,Human_Splice_Rec_143578,Human_Splice_Rec_143586,Human_Splice_Rec_143594 RMVar_hsa_circ_83029,RMVar_hsa_circ_104885,RMVar_hsa_circ_127038,RMVar_hsa_circ_84035,RMVar_hsa_circ_136895,RMVar_hsa_circ_136896,RMVar_hsa_circ_136897,RMVar_hsa_circ_136899,RMVar_hsa_circ_136898,RMVar_hsa_circ_345771 94087 RMVar_ID_94087 Human_SNP_ID_35037653 m1A Human chr1 - 156738615 156738615 156738615 CGCTATGGGATGAGCCCCCCAGGCTCTGTTGCAGACAAGAGGAAGAACCCCCCATGGATCAGGCG CGCTATGGGATGAGCCCCCCAGGCTCTGTTGCGGACAAGAGGAAGAACCCCCCATGGATCAGGCG T C MRPL24 Ensembl:ENSG00000143314 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156737517..156740427 26863196 MeRIP-seq:(Medium) rs559866026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329030,Human_RBP_ID_1413573,Human_RBP_ID_22431034,Human_RBP_ID_26801146 Human_Splice_Rec_143567,Human_Splice_Rec_143575,Human_Splice_Rec_143583,Human_Splice_Rec_143591,Human_Splice_Rec_143597 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897,RMVar_hsa_circ_269637 94088 RMVar_ID_94088 Human_SNP_ID_35037658 m1A Human chr1 - 156738627 156738627 156738627 CCCCCCCATTACCGCTATGGGATGAGCCCCCCAGGCTCTGTTGCAGACAAGAGGAAGAACCCCCC CCCCCCCATTACCGCTATGGGATGAGCCCCCCGGGCTCTGTTGCAGACAAGAGGAAGAACCCCCC T C MRPL24 Ensembl:ENSG00000143314 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156738576..156738775 26863196 MeRIP-seq:(Medium) rs1327235415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329030,Human_RBP_ID_971793,Human_RBP_ID_1413573,Human_RBP_ID_22431034,Human_RBP_ID_26801146 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897,RMVar_hsa_circ_269637 94089 RMVar_ID_94089 Human_SNP_ID_35037670 m1A Human chr1 - 156738652 156738652 156738652 GGCCTTGGCATCCAAGGTCACTCTGCCCCCCCATTACCGCTATGGGATGAGCCCCCCAGGCTCTG GGCCTTGGCATCCAAGGTCACTCTGCCCCCCCCTTACCGCTATGGGATGAGCCCCCCAGGCTCTG T G MRPL24 Ensembl:ENSG00000143314 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156738601..156738725 32194978 MeRIP-seq:(Medium) rs1558026811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4082945,Human_RBP_ID_5413097,Human_RBP_ID_22431034,Human_RBP_ID_26801146 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897,RMVar_hsa_circ_269637 94090 RMVar_ID_94090 Human_SNP_ID_35037728 m1A Human chr1 - 156738759 156738759 156738759 TGTTCCCGTTTCTATCCATCTGCCCAGAGCTGACAAGGAAGGTTTCGAGCGTTTTGCTGGCAAAG TGTTCCCGTTTCTATCCATCTGCCCAGAGCTGTCAAGGAAGGTTTCGAGCGTTTTGCTGGCAAAG T A MRPL24 Ensembl:ENSG00000143314 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK-293T cells,m1A-IP-seq;HEK293T,ALKBH3 KO chr1:156738657..156740427 31548705,26863410 m1A-IP-seq:(High) rs1369954782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17727566,Human_RBP_ID_24596111 Human_Splice_Rec_143566,Human_Splice_Rec_143574,Human_Splice_Rec_143582,Human_Splice_Rec_143590,Human_Splice_Rec_143596 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897,RMVar_hsa_circ_269637 94091 RMVar_ID_94091 Human_SNP_ID_35038250 m1A Human chr1 - 156740973 156740973 156740973 GAAGAGCCTATCCTTTTCCCTGGCCATGGCTCAGTCGCCTCCCCAGGGTTTATTTGCACCGGAAG GAAGAGCCTATCCTTTTCCCTGGCCATGGCTCGGTCGCCTCCCCAGGGTTTATTTGCACCGGAAG T C MRPL24 Ensembl:ENSG00000143314 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156740970..156741125 26863196 MeRIP-seq:(Medium) rs916945057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_143589 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897 94092 RMVar_ID_94092 Human_SNP_ID_35038276 m1A Human chr1 - 156741061 156741061 156741061 GGCCCATGTGCTGAAAATCCGAAGTGCCGCGGAAAGTGGAGGTGAGGGCCGCCCGCCCTAGAGGT GGCCCATGTGCTGAAAATCCGAAGTGCCGCGGCAAGTGGAGGTGAGGGCCGCCCGCCCTAGAGGT T G MRPL24 Ensembl:ENSG00000143314 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156740937..156741125;chr1:156740972..156741125 26863196 MeRIP-seq:(Medium) rs1183411943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074516,Human_RBP_ID_18415657,Human_RBP_ID_22431035,Human_RBP_ID_23206154 Human_Splice_Rec_143565,Human_Splice_Rec_143573 Human_miRNA_ID_2014711 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897 94093 RMVar_ID_94093 Human_SNP_ID_35038285 m1A Human chr1 + 156741076 156741075 156741076 GGCCCTCACCTCCACTTTCCGCGGCACTTCGGATTTTCAGCACATGGGCCCTCAGCGTCCCCTCC GGCCCTCACCTCCACTTTCCGCGGCACTTCGG_TTTTCAGCACATGGGCCCTCAGCGTCCCCTCC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156740938..156741125 26863196 MeRIP-seq:(Medium) rs1453467943 Functional Loss DEL dbSNP153 33..33 33 - - - 94094 RMVar_ID_94094 Human_SNP_ID_35038288 m1A Human chr1 + 156741076 156741076 156741076 GGCCCTCACCTCCACTTTCCGCGGCACTTCGGATTTTCAGCACATGGGCCCTCAGCGTCCCCTCC GGCCCTCACCTCCACTTTCCGCGGCACTTCGGCTTTTCAGCACATGGGCCCTCAGCGTCCCCTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156740938..156741125 26863196 MeRIP-seq:(Medium) rs1008936789 Functional Loss SNV dbSNP153 33..33 33 - - - 94095 RMVar_ID_94095 Human_SNP_ID_35038289 m1A Human chr1 + 156741076 156741076 156741076 GGCCCTCACCTCCACTTTCCGCGGCACTTCGGATTTTCAGCACATGGGCCCTCAGCGTCCCCTCC GGCCCTCACCTCCACTTTCCGCGGCACTTCGGGTTTTCAGCACATGGGCCCTCAGCGTCCCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:156740938..156741125 26863196 MeRIP-seq:(Medium) rs1008936789 Functional Loss SNV dbSNP153 33..33 33 - - - 94096 RMVar_ID_94096 Human_SNP_ID_35038665 m1A Human chr1 + 156742401 156742401 156742401 AGAAATGACACTGGAAGGAACATCAAAGCCCCAGCTACAAAAAGAAAGTCATCAAGCCCCAAATA AGAAATGACACTGGAAGGAACATCAAAGCCCCGGCTACAAAAAGAAAGTCATCAAGCCCCAAATA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156742351..156742550 26863196 MeRIP-seq:(Medium) rs1480491399 Functional Loss SNV dbSNP153 33..33 33 - - - 94097 RMVar_ID_94097 Human_SNP_ID_35038761 m1A Human chr1 + 156742833 156742833 156742833 AACTACAACTCCCAAAACTCTTGGGGTCGGCAAAAGGAAAAATGGGTGTTGTCAATCATCAAGGA AACTACAACTCCCAAAACTCTTGGGGTCGGCACAAGGAAAAATGGGTGTTGTCAATCATCAAGGA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:156742825..156742951;chr1:156742101..156742900 26863196 MeRIP-seq:(Medium) rs925345802 Functional Loss SNV dbSNP153 33..33 33 - - - 94098 RMVar_ID_94098 Human_SNP_ID_35038770 m1A Human chr1 + 156742921 156742920 156742921 TACAAGCTGTCCCACTTTCCCTGAATCTAGGCAGCTGGGATAATAGGTGTAGCAGGGGACAGGAG TACAAGCTGTCCCACTTTCCCTGAATCTAGGC_GCTGGGATAATAGGTGTAGCAGGGGACAGGAG CA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156742605..156742975 32194978 MeRIP-seq:(Medium) rs1242438081 Functional Loss DEL dbSNP153 33..33 33 - - - 94099 RMVar_ID_94099 Human_SNP_ID_35039063 m1A Human chr1 - 156743856 156743856 156743856 TCCTGCCTAGGACTCTCCTAAACGTCCCAAGGAGGCAGAAAACCCTGAAGGAGAGGAGAAGGAGG TCCTGCCTAGGACTCTCCTAAACGTCCCAAGGCGGCAGAAAACCCTGAAGGAGAGGAGAAGGAGG T G HDGF Ensembl:ENSG00000143321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:156743609..156743909;chr1:156743851..156743900 26863196 MeRIP-seq:(Medium) rs750355824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20978,Human_RBP_ID_855416,Human_RBP_ID_971825,Human_RBP_ID_1727101,Human_RBP_ID_3934185,Human_RBP_ID_5136886,Human_RBP_ID_8170769,Human_RBP_ID_9357043,Human_RBP_ID_18966127,Human_RBP_ID_22486143,Human_RBP_ID_22637662,Human_RBP_ID_26314844,Human_RBP_ID_26386574 Human_Splice_Rec_143606,Human_Splice_Rec_143616,Human_Splice_Rec_143626,Human_Splice_Rec_143640,Human_Splice_Rec_143650,Human_Splice_Rec_143654,Human_Splice_Rec_143662,Human_Splice_Rec_143674,Human_Splice_Rec_143684,Human_Splice_Rec_143690 RMVar_hsa_circ_82179,RMVar_hsa_circ_117608,RMVar_hsa_circ_108690,RMVar_hsa_circ_115770,RMVar_hsa_circ_99168,RMVar_hsa_circ_62751,RMVar_hsa_circ_136902,RMVar_hsa_circ_136904,RMVar_hsa_circ_136905,RMVar_hsa_circ_136903,RMVar_hsa_circ_136901,RMVar_hsa_circ_361976,RMVar_hsa_circ_363631,RMVar_hsa_circ_65078 94100 RMVar_ID_94100 Human_SNP_ID_35039174 m1A Human chr1 + 156744226 156744226 156744226 GCTCCTTTCTCGTTCTTCTCCTTGGCTGGCTCATCAATGACCAGCTTCCCTTCCTCGTCGCTGCT GCTCCTTTCTCGTTCTTCTCCTTGGCTGGCTCCTCAATGACCAGCTTCCCTTCCTCGTCGCTGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr1:156744146..156744389;chr1:156744134..156744386;chr1:156744151..156744275 26863196,32194978 MeRIP-seq:(Medium) rs544419635 Functional Loss SNV dbSNP153 33..33 33 - - - 94101 RMVar_ID_94101 Human_SNP_ID_35041322 m1A Human chr1 + 156751703 156751703 156751703 GTTTGAAATTCAATTGCTCCCTCCTCTGCGCGAGGCCTCTTCCTCCACCCCCCGCCCGGTCCCCA GTTTGAAATTCAATTGCTCCCTCCTCTGCGCGGGGCCTCTTCCTCCACCCCCCGCCCGGTCCCCA A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156751701..156751725 26863196 MeRIP-seq:(Medium) rs953956134 Functional Loss SNV dbSNP153 33..33 33 - - - 94102 RMVar_ID_94102 Human_SNP_ID_35045649 m1A Human chr1 - 156767858 156767858 156767858 GCGAACAAGCCCCCTAAAGCGGGCCCAGATGTAGGAGCCACCGCCTCCTCTTCCTCCGGCTCGGG GCGAACAAGCCCCCTAAAGCGGGCCCAGATGTGGGAGCCACCGCCTCCTCTTCCTCCGGCTCGGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156767853..156768200 26863196 MeRIP-seq:(Medium) rs1465424848 Functional Loss SNV dbSNP153 33..33 33 - - - 94103 RMVar_ID_94103 Human_SNP_ID_35045717 m1A Human chr1 + 156767951 156767951 156767951 TTGCTGCCTCCGCCCCCTCAGATGCTGGCGCCAGCCTTTCCCCCGCCGCTGTTGCTTCCCCCACC TTGCTGCCTCCGCCCCCTCAGATGCTGGCGCCGGCCTTTCCCCCGCCGCTGTTGCTTCCCCCACC A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156767780..156768188 26863196 MeRIP-seq:(Medium) rs904583520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222154,Human_RBP_ID_329112,Human_RBP_ID_18428741 Human_miRNA_ID_2145954,Human_miRNA_ID_2944824,Human_miRNA_ID_2987388,Human_miRNA_ID_3021079 RMVar_hsa_circ_136906,RMVar_hsa_circ_88557 94104 RMVar_ID_94104 Human_SNP_ID_35045741 m1A Human chr1 - 156768011 156767980 156768011 GGGAAGCCTCCCAGGCCGAAGGGCAAGGGGGGAGGAGGCTGAAGCCTGGGGTCTCCGGTGGGTGG GGGAAGCCTCCCAGGCCGAAGGGCAAGGGGGG_______________________________GG CACCCACCGGAGACCCCAGGCTTCAGCCTCCT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156767976..156768025 26863196 MeRIP-seq:(Medium) rs1553251805 Functional Loss DEL dbSNP153 33..63 33 - - - 94105 RMVar_ID_94105 Human_SNP_ID_35045747 m1A Human chr1 + 156767985 156767985 156767985 CCTTTCCCCCGCCGCTGTTGCTTCCCCCACCCACCGGAGACCCCAGGCTTCAGCCTCCTCCCCCC CCTTTCCCCCGCCGCTGTTGCTTCCCCCACCCCCCGGAGACCCCAGGCTTCAGCCTCCTCCCCCC A C PRCC Ensembl:ENSG00000143294 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:156767887..156768175 26863410 MeRIP-seq:(Medium) rs1390282491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222154,Human_RBP_ID_741357,Human_RBP_ID_971838,Human_RBP_ID_4083026,Human_RBP_ID_9319217,Human_RBP_ID_22531985,Human_RBP_ID_27389599 RMVar_hsa_circ_136906,RMVar_hsa_circ_88557 94106 RMVar_ID_94106 Human_SNP_ID_35045762 m1A Human chr1 - 156768011 156768011 156768011 GGGAAGCCTCCCAGGCCGAAGGGCAAGGGGGGAGGAGGCTGAAGCCTGGGGTCTCCGGTGGGTGG GGGAAGCCTCCCAGGCCGAAGGGCAAGGGGGGGGGAGGCTGAAGCCTGGGGTCTCCGGTGGGTGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156767976..156768025 26863196 MeRIP-seq:(Medium) rs1203085549 Functional Loss SNV dbSNP153 33..33 33 - - - 94107 RMVar_ID_94107 Human_SNP_ID_35045816 m1A Human chr1 - 156768105 156768105 156768105 CAGATTGAGGCCAGGGCCTCGGGGCGAGGGCAACCCCAATCCCAGTCCCTCCCCAACTCCCGCCG CAGATTGAGGCCAGGGCCTCGGGGCGAGGGCAGCCCCAATCCCAGTCCCTCCCCAACTCCCGCCG T C AL590666.5 Ensembl:ENSG00000287624 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156768076..156768200 26863196 MeRIP-seq:(Medium) rs754197287 Functional Loss SNV dbSNP153 33..33 33 - - - 94108 RMVar_ID_94108 Human_SNP_ID_35050450 m1A Human chr1 + 156786678 156786676 156786679 CCAACCTAAAAACCTGACTGTGAAAGAGACTAACAGGTTGCTCCTGCCCCATGCCTTCTCCCGCA CCAACCTAAAAACCTGACTGTGAAAGAGACT___AGGTTGCTCCTGCCCCATGCCTTCTCCCGCA TAAC T PRCC Ensembl:ENSG00000143294 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:156786676..156786700 26863196 MeRIP-seq:(Medium) rs1488785422 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1413664,Human_RBP_ID_1727120,Human_RBP_ID_3283315,Human_RBP_ID_4000324,Human_RBP_ID_18928722,Human_RBP_ID_23337015,Human_RBP_ID_27169804 Human_Splice_Rec_143694,Human_Splice_Rec_143700,Human_Splice_Rec_143712 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_323236,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908 94109 RMVar_ID_94109 Human_SNP_ID_35050488 m1A Human chr1 - 156786769 156786769 156786769 GTTGTGGTGCCCACAACAGGGGCAAGAGAGGAAGTCTTGGTCTTAGAAGCCAGTCTGGAGGGCTT GTTGTGGTGCCCACAACAGGGGCAAGAGAGGACGTCTTGGTCTTAGAAGCCAGTCTGGAGGGCTT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156786735..156786861 26863196 MeRIP-seq:(Medium) rs766921423 Functional Loss SNV dbSNP153 33..33 33 - - - 94110 RMVar_ID_94110 Human_SNP_ID_35050529 m1A Human chr1 + 156786885 156786883 156786886 GCAGGTGACAAAGCAGATCACGCAGGAAGAAGACGACAGTGATGAGGAAGTAGCCCCCGAAAACT GCAGGTGACAAAGCAGATCACGCAGGAAGAA___GACAGTGATGAGGAAGTAGCCCCCGAAAACT AGAC A PRCC Ensembl:ENSG00000143294 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156786632..156787037 26863196 MeRIP-seq:(Medium) rs1174966649 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_329122,Human_RBP_ID_5697834,Human_RBP_ID_10610540,Human_RBP_ID_22129471,Human_RBP_ID_27169809 Human_miRNA_ID_2997197 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_323236,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908 94111 RMVar_ID_94111 Human_SNP_ID_35050584 m1A Human chr1 + 156787035 156787035 156787035 AGGCACGGAACCAGAGCCGGCTTTCCAGGACGATGCAGCCAATGCCCCCCTTGAATTCAAGATGG AGGCACGGAACCAGAGCCGGCTTTCCAGGACGTTGCAGCCAATGCCCCCCTTGAATTCAAGATGG A T PRCC Ensembl:ENSG00000143294 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156786984..156787083 32194978 MeRIP-seq:(Medium) rs896261026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329127,Human_RBP_ID_971844,Human_RBP_ID_1727121,Human_RBP_ID_4000341,Human_RBP_ID_5697837,Human_RBP_ID_8287662,Human_RBP_ID_8735875,Human_RBP_ID_9357047,Human_RBP_ID_10610546,Human_RBP_ID_17212957,Human_RBP_ID_17727634,Human_RBP_ID_22023927,Human_RBP_ID_23337017,Human_RBP_ID_24360613,Human_RBP_ID_27169813,Human_RBP_ID_27389621,Human_RBP_ID_27579555 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_323236,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908 94112 RMVar_ID_94112 Human_SNP_ID_35051369 m1A Human chr1 + 156789434 156789434 156789434 GTGGAAGAGGACTGGTATCTAATCTTAGAATTACAAGATAGCTTCCTGAAATGTGGATGATGAGG GTGGAAGAGGACTGGTATCTAATCTTAGAATTGCAAGATAGCTTCCTGAAATGTGGATGATGAGG A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156789429..156789632 26863196 MeRIP-seq:(Medium) rs1323682781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5697856,Human_RBP_ID_10610647 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908 94113 RMVar_ID_94113 Human_SNP_ID_35052647 m1A Human chr1 + 156794761 156794761 156794761 GTGATGACCAGCTCAGTGGGGCCCAGCAATGGATGACTAAGTCATTGACAGAAGAGAAAACCATG GTGATGACCAGCTCAGTGGGGCCCAGCAATGGGTGACTAAGTCATTGACAGAAGAGAAAACCATG A G PRCC Ensembl:ENSG00000143294 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156794711..156794845 26863196 MeRIP-seq:(Medium) rs769121851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329130,Human_RBP_ID_1413677,Human_RBP_ID_1727128,Human_RBP_ID_3283326,Human_RBP_ID_5332060,Human_RBP_ID_10610859,Human_RBP_ID_18553668,Human_RBP_ID_23337032,Human_RBP_ID_26312033,Human_RBP_ID_27798669 Human_Splice_Rec_143704,Human_Splice_Rec_143705,Human_Splice_Rec_143714,Human_Splice_Rec_143715,Human_Splice_Rec_143724,Human_Splice_Rec_143725,Human_Splice_Rec_143730 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908,RMVar_hsa_circ_102368,RMVar_hsa_circ_118873,RMVar_hsa_circ_281789,RMVar_hsa_circ_136909,RMVar_hsa_circ_136910 94114 RMVar_ID_94114 Human_SNP_ID_35052649 m1A Human chr1 + 156794772 156794772 156794772 CTCAGTGGGGCCCAGCAATGGATGACTAAGTCATTGACAGAAGAGAAAACCATGAAGTCATTCAG CTCAGTGGGGCCCAGCAATGGATGACTAAGTCGTTGACAGAAGAGAAAACCATGAAGTCATTCAG A G PRCC Ensembl:ENSG00000143294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156794721..156794854 26863196 MeRIP-seq:(Medium) rs777177184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329130,Human_RBP_ID_1413678,Human_RBP_ID_1727128,Human_RBP_ID_5332060,Human_RBP_ID_26312033,Human_RBP_ID_27798669 Human_Splice_Rec_143705,Human_Splice_Rec_143715,Human_Splice_Rec_143725 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908,RMVar_hsa_circ_102368,RMVar_hsa_circ_118873,RMVar_hsa_circ_281789,RMVar_hsa_circ_136909,RMVar_hsa_circ_136910 94115 RMVar_ID_94115 Human_SNP_ID_35052650 m1A Human chr1 + 156794772 156794772 156794772 CTCAGTGGGGCCCAGCAATGGATGACTAAGTCATTGACAGAAGAGAAAACCATGAAGTCATTCAG CTCAGTGGGGCCCAGCAATGGATGACTAAGTCTTTGACAGAAGAGAAAACCATGAAGTCATTCAG A T PRCC Ensembl:ENSG00000143294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156794721..156794854 26863196 MeRIP-seq:(Medium) rs777177184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329130,Human_RBP_ID_1413678,Human_RBP_ID_1727128,Human_RBP_ID_5332060,Human_RBP_ID_26312033,Human_RBP_ID_27798669 Human_Splice_Rec_143705,Human_Splice_Rec_143715,Human_Splice_Rec_143725 RMVar_hsa_circ_31039,RMVar_hsa_circ_136906,RMVar_hsa_circ_88557,RMVar_hsa_circ_97987,RMVar_hsa_circ_84794,RMVar_hsa_circ_136907,RMVar_hsa_circ_136908,RMVar_hsa_circ_102368,RMVar_hsa_circ_118873,RMVar_hsa_circ_281789,RMVar_hsa_circ_136909,RMVar_hsa_circ_136910 94116 RMVar_ID_94116 Human_SNP_ID_35053129 m1A Human chr1 - 156796641 156796641 156796641 TTAGAAATTTCACAATCACTCTACCTCTCCCCAGTCTTCCAGCCTCCGCCCGTAACTGCACTGAA TTAGAAATTTCACAATCACTCTACCTCTCCCCTGTCTTCCAGCCTCCGCCCGTAACTGCACTGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156796640..156796941 26863196 MeRIP-seq:(Medium) rs1049932548 Functional Loss SNV dbSNP153 33..33 33 - - - 94117 RMVar_ID_94117 Human_SNP_ID_35053130 m1A Human chr1 - 156796641 156796641 156796641 TTAGAAATTTCACAATCACTCTACCTCTCCCCAGTCTTCCAGCCTCCGCCCGTAACTGCACTGAA TTAGAAATTTCACAATCACTCTACCTCTCCCCCGTCTTCCAGCCTCCGCCCGTAACTGCACTGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156796640..156796941 26863196 MeRIP-seq:(Medium) rs1049932548 Functional Loss SNV dbSNP153 33..33 33 - - - 94118 RMVar_ID_94118 Human_SNP_ID_35055896 m1A Human chr1 - 156809426 156809426 156809426 CCCCGCCAAACCTCAGCTGCCCCCAGAAGTCTACACAATCCCTGTTCCACGACACCGCCCGGCCC CCCCGCCAAACCTCAGCTGCCCCCAGAAGTCTGCACAATCCCTGTTCCACGACACCGCCCGGCCC T C SH2D2A Ensembl:ENSG00000027869 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156809391..156809538 26863196 MeRIP-seq:(Medium) rs759965228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_143746,Human_Splice_Rec_143762,Human_Splice_Rec_143778,Human_Splice_Rec_143786 RMVar_hsa_circ_55300 94119 RMVar_ID_94119 Human_SNP_ID_35056574 m1A Human chr1 + 156812401 156812401 156812401 CATCTCCTACCTCTCTATCCCTCAGTCACCGGATCCACCCATGCTAACTTCCTCTCTGCTCCCAT CATCTCCTACCTCTCTATCCCTCAGTCACCGGCTCCACCCATGCTAACTTCCTCTCTGCTCCCAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156812399..156812508 26863196 MeRIP-seq:(Medium) rs1490549102 Functional Loss SNV dbSNP153 33..33 33 - - - 94120 RMVar_ID_94120 Human_SNP_ID_35056930 m1A Human chr1 + 156814003 156814003 156814003 GTCCCTGAGCTGGGCCAGCAGGAAGTGGCGGCAGCAAGTCCGGCTCCTGGAGGGCGCCGTTAGGG GTCCCTGAGCTGGGCCAGCAGGAAGTGGCGGCGGCAAGTCCGGCTCCTGGAGGGCGCCGTTAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156813971..156814093 26863196 MeRIP-seq:(Medium) rs1316741212 Functional Loss SNV dbSNP153 33..33 33 - - - 94121 RMVar_ID_94121 Human_SNP_ID_35083047 m1A Human chr1 + 156907697 156907697 156907697 TCTTGCCAAAATGGAGGTGTCTTCCAAACCCCACAGGGCTCCTGCAGCTGCCCCCCTGGCTGGAT TCTTGCCAAAATGGAGGTGTCTTCCAAACCCCCCAGGGCTCCTGCAGCTGCCCCCCTGGCTGGAT A C PEAR1 Ensembl:ENSG00000187800 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156907662..156907747 26863196 MeRIP-seq:(Medium) rs1186644695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_144068,Human_Splice_Rec_144069,Human_Splice_Rec_144122,Human_Splice_Rec_144123,Human_Splice_Rec_144158,Human_Splice_Rec_144159 94122 RMVar_ID_94122 Human_SNP_ID_35103371 m1A Human chr1 - 156978169 156978168 156978169 AATAATCCTCCTGGCTTTCTTTCCTCACCCTAATGTCCTGTTGAAAAGCTCCGCATTGGGGAGGA AATAATCCTCCTGGCTTTCTTTCCTCACCCTA_TGTCCTGTTGAAAAGCTCCGCATTGGGGAGGA AT A ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156978165..156978288 26863196 MeRIP-seq:(Medium) rs1377239558 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82735,RMVar_hsa_circ_14778,RMVar_hsa_circ_81487,RMVar_hsa_circ_111368,RMVar_hsa_circ_136921,RMVar_hsa_circ_76961,RMVar_hsa_circ_136923,RMVar_hsa_circ_87290,RMVar_hsa_circ_136924,RMVar_hsa_circ_136927,RMVar_hsa_circ_116431,RMVar_hsa_circ_136929,RMVar_hsa_circ_136931,RMVar_hsa_circ_104248,RMVar_hsa_circ_136937,RMVar_hsa_circ_82574,RMVar_hsa_circ_136939,RMVar_hsa_circ_344510,RMVar_hsa_circ_336875,RMVar_hsa_circ_113353,RMVar_hsa_circ_136940,RMVar_hsa_circ_76567,RMVar_hsa_circ_136941,RMVar_hsa_circ_136942,RMVar_hsa_circ_56235,RMVar_hsa_circ_295316,RMVar_hsa_circ_136943 94123 RMVar_ID_94123 Human_SNP_ID_35103372 m1A Human chr1 - 156978169 156978169 156978169 AATAATCCTCCTGGCTTTCTTTCCTCACCCTAATGTCCTGTTGAAAAGCTCCGCATTGGGGAGGA AATAATCCTCCTGGCTTTCTTTCCTCACCCTAGTGTCCTGTTGAAAAGCTCCGCATTGGGGAGGA T C ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156978165..156978288 26863196 MeRIP-seq:(Medium) rs373423595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82735,RMVar_hsa_circ_14778,RMVar_hsa_circ_81487,RMVar_hsa_circ_111368,RMVar_hsa_circ_136921,RMVar_hsa_circ_76961,RMVar_hsa_circ_136923,RMVar_hsa_circ_87290,RMVar_hsa_circ_136924,RMVar_hsa_circ_136927,RMVar_hsa_circ_116431,RMVar_hsa_circ_136929,RMVar_hsa_circ_136931,RMVar_hsa_circ_104248,RMVar_hsa_circ_136937,RMVar_hsa_circ_82574,RMVar_hsa_circ_136939,RMVar_hsa_circ_344510,RMVar_hsa_circ_336875,RMVar_hsa_circ_113353,RMVar_hsa_circ_136940,RMVar_hsa_circ_76567,RMVar_hsa_circ_136941,RMVar_hsa_circ_136942,RMVar_hsa_circ_56235,RMVar_hsa_circ_295316,RMVar_hsa_circ_136943 94124 RMVar_ID_94124 Human_SNP_ID_35104029 m1A Human chr1 - 156980828 156980828 156980828 AGTAAACTCATTTCCCCCCCCCCCCCCGGAATATAACTGATTTGACCTTGGAACATATCCAGATA AGTAAACTCATTTCCCCCCCCCCCCCCGGAATGTAACTGATTTGACCTTGGAACATATCCAGATA T C ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:156980826..156980850 26863196 MeRIP-seq:(Medium) rs1289517348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14778,RMVar_hsa_circ_111368,RMVar_hsa_circ_136924,RMVar_hsa_circ_82574,RMVar_hsa_circ_136939,RMVar_hsa_circ_336875,RMVar_hsa_circ_136940,RMVar_hsa_circ_295316,RMVar_hsa_circ_136943,RMVar_hsa_circ_359574 94125 RMVar_ID_94125 Human_SNP_ID_35111676 m1A Human chr1 + 157013444 157013444 157013444 AAAAACTCCTGCTTATTCCTCAAGCCCCTATGAATTCCTCAAACATTAATGCTTCTTGGTGAAGC AAAAACTCCTGCTTATTCCTCAAGCCCCTATGTATTCCTCAAACATTAATGCTTCTTGGTGAAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:157013441..157013633 26863196 MeRIP-seq:(Medium) rs1443549531 Functional Loss SNV dbSNP153 33..33 33 - - - 94126 RMVar_ID_94126 Human_SNP_ID_35111729 m1A Human chr1 - 157013725 157013725 157013725 AGGAAACTGGAGCCTGTGTTTTTGAAGGTGGAAGTATTGTGAGCAATGTCAAGATTCAAAATGTA AGGAAACTGGAGCCTGTGTTTTTGAAGGTGGAGGTATTGTGAGCAATGTCAAGATTCAAAATGTA T C ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:157013722..157013845 26863196 MeRIP-seq:(Medium) rs1450104221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23337195 RMVar_hsa_circ_127797,RMVar_hsa_circ_136946 94127 RMVar_ID_94127 Human_SNP_ID_35117354 m1A Human chr1 - 157037348 157037348 157037348 TTATGTATTATATGGTGATAAACATAGTGTTTAAAGAGAGAATTCTGATATTAATATATAGAGCA TTATGTATTATATGGTGATAAACATAGTGTTTGAAGAGAGAATTCTGATATTAATATATAGAGCA T C ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:157037345..157037529 26863196 MeRIP-seq:(Medium) rs1262206802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127797,RMVar_hsa_circ_136946 94128 RMVar_ID_94128 Human_SNP_ID_35117367 m1A Human chr1 + 157037408 157037408 157037408 CATAAACCTTCCCCGGCTCCCTTTCTACTACCACATAAAGTCTGAATCCCTTCATTCTCCCTACC CATAAACCTTCCCCGGCTCCCTTTCTACTACCGCATAAAGTCTGAATCCCTTCATTCTCCCTACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:157037379..157037582 26863196 MeRIP-seq:(Medium) rs1298008216 Functional Loss SNV dbSNP153 33..33 33 - - - 94129 RMVar_ID_94129 Human_SNP_ID_35138950 m1A Human chr1 - 157125363 157125363 157125363 CCACTGCAGTGCCAAATGCATCCTGAGGAGTCAACTCAGTTCTCCATCAAGCTGCAGCCCCCACC CCACTGCAGTGCCAAATGCATCCTGAGGAGTCGACTCAGTTCTCCATCAAGCTGCAGCCCCCACC T C ETV3 Ensembl:ENSG00000117036 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:157125313..157125513 32194978 MeRIP-seq:(Medium) rs1427938789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329210,Human_RBP_ID_27800957 Human_miRNA_ID_203353,Human_miRNA_ID_1488554 94130 RMVar_ID_94130 Human_SNP_ID_35139009 m1A Human chr1 + 157125570 157125570 157125570 CCTGGTGATGGGCTATAGGAGAAGATGGTGGGAGTCAGGGAGAGGGCTGGTGAAATGGGGACATT CCTGGTGATGGGCTATAGGAGAAGATGGTGGGGGTCAGGGAGAGGGCTGGTGAAATGGGGACATT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:157125519..157125634 26863196 MeRIP-seq:(Medium) rs1359784094 Functional Loss SNV dbSNP153 33..33 33 - - - 94131 RMVar_ID_94131 Human_SNP_ID_35142107 m1A Human chr1 - 157138342 157138342 157138342 GGAGGAGCCGGAGACGCCGCGGAGGAGACCGGACCGAAGACGGACCGTGCCGGGAAGAGGTGAGT GGAGGAGCCGGAGACGCCGCGGAGGAGACCGGCCCGAAGACGGACCGTGCCGGGAAGAGGTGAGT T G ETV3 Ensembl:ENSG00000117036 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:157135662..157138584 26863196 MeRIP-seq:(Medium) rs1256998274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18415660,Human_RBP_ID_26314849 Human_Splice_Rec_144515,Human_Splice_Rec_144523,Human_Splice_Rec_144529 94132 RMVar_ID_94132 Human_SNP_ID_35355724 m1A Human chr1 - 157995935 157995935 157995935 CCTGCCAAGCTCTCCACCCCCATGTGTGTCCCAGTCTCCCCAGACCCCTACTCCTTCCCTCTCTG CCTGCCAAGCTCTCCACCCCCATGTGTGTCCCGGTCTCCCCAGACCCCTACTCCTTCCCTCTCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:157995753..157996139 26863196 MeRIP-seq:(Medium) rs1245894280 Functional Loss SNV dbSNP153 33..33 33 - - - 94133 RMVar_ID_94133 Human_SNP_ID_35356948 m1A Human chr1 + 158001483 158001483 158001483 AGCAGGTGGTCCTTCCCTTTTAAGAAACTAAGATATACACACATGAAGACTGCTGGTGGTGCAAG AGCAGGTGGTCCTTCCCTTTTAAGAAACTAAGGTATACACACATGAAGACTGCTGGTGGTGCAAG A G KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:158001477..158001787 26863196 MeRIP-seq:(Medium) rs1030291048 Functional Loss SNV dbSNP153 33..33 33 - - - 94134 RMVar_ID_94134 Human_SNP_ID_35359834 m1A Human chr1 + 158014062 158014046 158014062 GGGGATTAGGACCAGTTTGGAAGCCCAAAGATATGGGAGAGGGCTTAGTAAGAAGGCAGGTGGAA GGGGATTAGGACCAGTT________________TGGGAGAGGGCTTAGTAAGAAGGCAGGTGGAA TTGGAAGCCCAAAGATA T KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:158014060..158014199 26863196 MeRIP-seq:(Medium) rs1182845777 Functional Loss DEL dbSNP153 18..33 33 - - - 94135 RMVar_ID_94135 Human_SNP_ID_35359844 m1A Human chr1 + 158014080 158014080 158014080 GGAAGCCCAAAGATATGGGAGAGGGCTTAGTAAGAAGGCAGGTGGAAGGAGGAAATGAGAGAATG GGAAGCCCAAAGATATGGGAGAGGGCTTAGTACGAAGGCAGGTGGAAGGAGGAAATGAGAGAATG A C KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:158014070..158014224 26863196 MeRIP-seq:(Medium) rs921053715 Functional Loss SNV dbSNP153 33..33 33 - - - 94136 RMVar_ID_94136 Human_SNP_ID_35362534 m1A Human chr1 + 158025433 158025433 158025433 GCAGGAGAAGCAAGGAACTGAAGACTCTGAGGAGGGACAAAGGCTAAGGGTGCCCCAGGGAGAAG GCAGGAGAAGCAAGGAACTGAAGACTCTGAGGGGGGACAAAGGCTAAGGGTGCCCCAGGGAGAAG A G KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:158025348..158025764 26863196 MeRIP-seq:(Medium) rs1341121325 Functional Loss SNV dbSNP153 33..33 33 - - - 94137 RMVar_ID_94137 Human_SNP_ID_35362584 m1A Human chr1 + 158025653 158025653 158025653 GACGAGGCCAGGCGGGAAGAGATGCAGCCAAGAGCAGCACCGAAGAGGAGAAGCAGAGGCCAGAG GACGAGGCCAGGCGGGAAGAGATGCAGCCAAGGGCAGCACCGAAGAGGAGAAGCAGAGGCCAGAG A G KIRREL1-IT1,KIRREL1 Ensembl:ENSG00000226520,Ensembl:ENSG00000183853 lincRNA,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:158025273..158025816 26863196 MeRIP-seq:(Medium) rs779994140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_145261 94138 RMVar_ID_94138 Human_SNP_ID_35367268 m1A Human chr1 + 158044988 158044984 158044988 AGTGGTCCAATTTTAAGTAGTGCAGTGAGTAAAGAACTTACTCAGAAGGTGATAACAAGAAAAGA AGTGGTCCAATTTTAAGTAGTGCAGTGAG____GAACTTACTCAGAAGGTGATAACAAGAAAAGA GTAAA G KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:158044980..158045095 26863196 MeRIP-seq:(Medium) rs372222104 Functional Loss DEL dbSNP153 30..33 33 - - - 94139 RMVar_ID_94139 Human_SNP_ID_35367581 m1A Human chr1 + 158046571 158046571 158046571 GTTGAATTTAACAAGGGAGCGAACCAAGAGGGAGGGGAGGGCCAGTCAGGACCCTTCAACAAGAA GTTGAATTTAACAAGGGAGCGAACCAAGAGGGCGGGGAGGGCCAGTCAGGACCCTTCAACAAGAA A C KIRREL1 Ensembl:ENSG00000183853 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:158046566..158046745 26863196 MeRIP-seq:(Medium) rs952437564 Functional Loss SNV dbSNP153 33..33 33 - - - 94140 RMVar_ID_94140 Human_SNP_ID_35377186 m1A Human chr1 - 158088029 158088029 158088029 TTGTCTCATAGCGACTCTCGTGGGCGTCTTCAATCAAGAAACCCCCTTTGGCCCACCTAGGGGAG TTGTCTCATAGCGACTCTCGTGGGCGTCTTCATTCAAGAAACCCCCTTTGGCCCACCTAGGGGAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:158088026..158088100 32194978 MeRIP-seq:(Medium) rs761695279 Functional Loss SNV dbSNP153 33..33 33 - - - 94141 RMVar_ID_94141 Human_SNP_ID_35377187 m1A Human chr1 - 158088029 158088029 158088029 TTGTCTCATAGCGACTCTCGTGGGCGTCTTCAATCAAGAAACCCCCTTTGGCCCACCTAGGGGAG TTGTCTCATAGCGACTCTCGTGGGCGTCTTCAGTCAAGAAACCCCCTTTGGCCCACCTAGGGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:158088026..158088100 32194978 MeRIP-seq:(Medium) rs761695279 Functional Loss SNV dbSNP153 33..33 33 - - - 94142 RMVar_ID_94142 Human_SNP_ID_35823828 m1A Human chr1 - 159781207 159781207 159781207 GCCCGCGCTCCGTCAGGGACACCAGGTGCCGCACGCCCAGGTCCAACAGGAACTGGTAGTGGGCG GCCCGCGCTCCGTCAGGGACACCAGGTGCCGCTCGCCCAGGTCCAACAGGAACTGGTAGTGGGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:159781158..159781277 26863196 MeRIP-seq:(Medium) rs1416308866 Functional Loss SNV dbSNP153 33..33 33 - - - 94143 RMVar_ID_94143 Human_SNP_ID_35843537 m1A Human chr1 + 159855983 159855980 159855983 ACCGCGGGCGCCGCCAGCCCCGGAGCCCCCGCAGCAGCAGCAGACGAGCCCCCAGATGCCTACGG ACCGCGGGCGCCGCCAGCCCCGGAGCCCCC___GCAGCAGCAGACGAGCCCCCAGATGCCTACGG CGCA C AL590560.3 Ensembl:ENSG00000272668 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:159855934..159856066 26863196 MeRIP-seq:(Medium) rs774629452 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_146338 94144 RMVar_ID_94144 Human_SNP_ID_35843545 m1A Human chr1 - 159856007 159856007 159856007 CTCTGCTCGCGCTGGGCTGCCTGGCCGTAGGCATCTGGGGGCTCGTCTGCTGCTGCTGCGGGGGC CTCTGCTCGCGCTGGGCTGCCTGGCCGTAGGCTTCTGGGGGCTCGTCTGCTGCTGCTGCGGGGGC T A AL590560.2,VSIG8 Ensembl:ENSG00000256029,Ensembl:ENSG00000243284 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:159855959..159856056 26863196 MeRIP-seq:(Medium) rs1341170360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_146282,Human_Splice_Rec_146334 94145 RMVar_ID_94145 Human_SNP_ID_35850613 m1A Human chr1 - 159884488 159884486 159884489 GCGATCGCTGCTTGCTGAGCAGCGGGAGCAGGAGAAGGAGCAGATGCTGGAATATATGGAACAGC GCGATCGCTGCTTGCTGAGCAGCGGGAGCAG___AAGGAGCAGATGCTGGAATATATGGAACAGC TCTC T CFAP45 Ensembl:ENSG00000213085 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:159884436..159884547 26863196 MeRIP-seq:(Medium) rs753806120 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_146354,Human_Splice_Rec_146355,Human_Splice_Rec_146376,Human_Splice_Rec_146377,Human_Splice_Rec_146398,Human_Splice_Rec_146399 94146 RMVar_ID_94146 Human_SNP_ID_35858704 m1A Human chr1 + 159918773 159918773 159918773 ATATATCTACATATATATTAACCATTCGTGGGAGGGCAGGGGCAAGGCCTGGGGTGGGATCAGAG ATATATCTACATATATATTAACCATTCGTGGGCGGGCAGGGGCAAGGCCTGGGGTGGGATCAGAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:159918726..159918925 32194978 MeRIP-seq:(Medium) rs970685163 Functional Loss SNV dbSNP153 33..33 33 - - - 94147 RMVar_ID_94147 Human_SNP_ID_35858719 m1A Human chr1 - 159918808 159918808 159918808 CAGGCATGACTGGCTACGGGATGCCACGCCAGATCCTCTGATCCCACCCCAGGCCTTGCCCCTGC CAGGCATGACTGGCTACGGGATGCCACGCCAGGTCCTCTGATCCCACCCCAGGCCTTGCCCCTGC T C TAGLN2 Ensembl:ENSG00000158710 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:159918758..159918877 26863196 MeRIP-seq:(Medium) rs773234892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222512,Human_RBP_ID_329411,Human_RBP_ID_743558,Human_RBP_ID_4083190,Human_RBP_ID_8287878,Human_RBP_ID_22427625,Human_RBP_ID_23337600,Human_RBP_ID_27152873,Human_RBP_ID_27389860 Human_miRNA_ID_2567739 RMVar_hsa_circ_136988,RMVar_hsa_circ_97163,RMVar_hsa_circ_113441,RMVar_hsa_circ_120380,RMVar_hsa_circ_106752,RMVar_hsa_circ_90034,RMVar_hsa_circ_136989,RMVar_hsa_circ_136986,RMVar_hsa_circ_136987,RMVar_hsa_circ_136990,RMVar_hsa_circ_136985,RMVar_hsa_circ_378704 94148 RMVar_ID_94148 Human_SNP_ID_35858872 m1A Human chr1 + 159919337 159919337 159919337 GCCCATCATCTCGGGCTACTGCCAGCCCACCCAGATTCATCAGCGTCCGCTGCACACAGGCCATG GCCCATCATCTCGGGCTACTGCCAGCCCACCCGGATTCATCAGCGTCCGCTGCACACAGGCCATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:159919273..159919389;chr1:159919276..159919400 26863196 MeRIP-seq:(Medium) rs1174074445 Functional Loss SNV dbSNP153 33..33 33 - - - 94149 RMVar_ID_94149 Human_SNP_ID_35858873 m1A Human chr1 + 159919339 159919339 159919339 CCATCATCTCGGGCTACTGCCAGCCCACCCAGATTCATCAGCGTCCGCTGCACACAGGCCATGTT CCATCATCTCGGGCTACTGCCAGCCCACCCAGGTTCATCAGCGTCCGCTGCACACAGGCCATGTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:159919301..159919400 26863196 MeRIP-seq:(Medium) rs764239031 Functional Loss SNV dbSNP153 33..33 33 - - - 94150 RMVar_ID_94150 Human_SNP_ID_35859205 m1A Human chr1 - 159920445 159920445 159920445 CCGGGAGGTGCAGCAGAAGATTGAGAAACAATATGATGCAGATCTGGAGCAGATCCTGATCCAGT CCGGGAGGTGCAGCAGAAGATTGAGAAACAATGTGATGCAGATCTGGAGCAGATCCTGATCCAGT T C TAGLN2 Ensembl:ENSG00000158710 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:159920394..159920581 26863196 MeRIP-seq:(Medium) rs1337124522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1150086,Human_RBP_ID_1413775,Human_RBP_ID_1727273,Human_RBP_ID_4074530,Human_RBP_ID_5698817,Human_RBP_ID_22431050,Human_RBP_ID_22848585 Human_Splice_Rec_146428,Human_Splice_Rec_146436,Human_Splice_Rec_146444,Human_Splice_Rec_146450,Human_Splice_Rec_146458 RMVar_hsa_circ_136988,RMVar_hsa_circ_113441,RMVar_hsa_circ_90034,RMVar_hsa_circ_136989,RMVar_hsa_circ_136990,RMVar_hsa_circ_378704,RMVar_hsa_circ_289074,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_323290,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 94151 RMVar_ID_94151 Human_SNP_ID_35859209 m1A Human chr1 - 159920466 159920466 159920466 GGGACCTGCATATGGCCTGAGCCGGGAGGTGCAGCAGAAGATTGAGAAACAATATGATGCAGATC GGGACCTGCATATGGCCTGAGCCGGGAGGTGCGGCAGAAGATTGAGAAACAATATGATGCAGATC T C TAGLN2 Ensembl:ENSG00000158710 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11556958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329433,Human_RBP_ID_1413775,Human_RBP_ID_1727273,Human_RBP_ID_3283496,Human_RBP_ID_4074530,Human_RBP_ID_5311875,Human_RBP_ID_5698817,Human_RBP_ID_8287885,Human_RBP_ID_18187826,Human_RBP_ID_18428760,Human_RBP_ID_18553865,Human_RBP_ID_19151784,Human_RBP_ID_22427633,Human_RBP_ID_26844389,Human_RBP_ID_27170011,Human_RBP_ID_27389871 Human_Splice_Rec_146428,Human_Splice_Rec_146436,Human_Splice_Rec_146444,Human_Splice_Rec_146450,Human_Splice_Rec_146458 Human_miRNA_ID_2749958 RMVar_hsa_circ_136988,RMVar_hsa_circ_113441,RMVar_hsa_circ_90034,RMVar_hsa_circ_136989,RMVar_hsa_circ_136990,RMVar_hsa_circ_378704,RMVar_hsa_circ_289074,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_323290,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 94152 RMVar_ID_94152 Human_SNP_ID_35859222 m1A Human chr1 - 159920502 159920502 159920502 CCCGCAGCCACCGCCACCCATTGGAATGGCCAACAGGGGACCTGCATATGGCCTGAGCCGGGAGG CCCGCAGCCACCGCCACCCATTGGAATGGCCAGCAGGGGACCTGCATATGGCCTGAGCCGGGAGG T C TAGLN2 Ensembl:ENSG00000158710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:159920451..159920550 26863196 MeRIP-seq:(Medium) rs765357705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21939,Human_RBP_ID_4074531,Human_RBP_ID_5311875,Human_RBP_ID_9319219,Human_RBP_ID_18187316,Human_RBP_ID_22532170 Human_Splice_Rec_146428,Human_Splice_Rec_146436,Human_Splice_Rec_146444,Human_Splice_Rec_146450,Human_Splice_Rec_146458 Human_miRNA_ID_2392187 RMVar_hsa_circ_136988,RMVar_hsa_circ_113441,RMVar_hsa_circ_90034,RMVar_hsa_circ_136989,RMVar_hsa_circ_136990,RMVar_hsa_circ_378704,RMVar_hsa_circ_289074,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_323290,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 94153 RMVar_ID_94153 Human_SNP_ID_35859236 m1A Human chr1 + 159920536 159920536 159920536 GGCCATTCCAATGGGTGGCGGTGGCTGCGGGGAGCTAGGGAGAGGACACACCCGGGCTTTTGGTC GGCCATTCCAATGGGTGGCGGTGGCTGCGGGGTGCTAGGGAGAGGACACACCCGGGCTTTTGGTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:159920290..159923473;chr1:159920376..159920576;chr1:159920404..159920550 26863196 MeRIP-seq:(Medium) rs754720025 Functional Loss SNV dbSNP153 33..33 33 - - - 94154 RMVar_ID_94154 Human_SNP_ID_35860390 m1A Human chr1 - 159925320 159925320 159925320 AAGGGCTGGTACCAGGCAAGGGTCCGGTGACTACTTTACCCCGCCCCGTGCTGTCAGGTCCTGTC AAGGGCTGGTACCAGGCAAGGGTCCGGTGACTGCTTTACCCCGCCCCGTGCTGTCAGGTCCTGTC T C TAGLN2 Ensembl:ENSG00000158710 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:159925318..159925550 26863196 MeRIP-seq:(Medium) rs3789039 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - GWAS_ID_12241,GWAS_ID_12242,GWAS_ID_12243,GWAS_ID_12244 RMVar_hsa_circ_113441,RMVar_hsa_circ_136989,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 94155 RMVar_ID_94155 Human_SNP_ID_35860409 m1A Human chr1 - 159925391 159925391 159925391 GGGGACATGTGCGTGCTGTGTAGAAAGCAAGAAGCCAGCGCTTTGAACTTGCTCCAGCGAGCTCG GGGGACATGTGCGTGCTGTGTAGAAAGCAAGAGGCCAGCGCTTTGAACTTGCTCCAGCGAGCTCG T C TAGLN2 Ensembl:ENSG00000158710 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:159925387..159925550 26863196 MeRIP-seq:(Medium) rs1361068635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113441,RMVar_hsa_circ_136989,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 94156 RMVar_ID_94156 Human_SNP_ID_35886620 m1A Human chr1 + 160031856 160031856 160031856 GGCCGCCGCATCTCCCACCCGCCAGGCTGCCAACCGAAACGACTGCAGACTATCACATCCGGCAT GGCCGCCGCATCTCCCACCCGCCAGGCTGCCAGCCGAAACGACTGCAGACTATCACATCCGGCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:160031742..160031952 26863196 MeRIP-seq:(Medium) rs536135478 Functional Loss SNV dbSNP153 33..33 33 - - - 94157 RMVar_ID_94157 Human_SNP_ID_35901196 m1A Human chr1 - 160093851 160093851 160093851 GTCTGGGCAAGGAAGGGACCGATCGGTACCGCATGGTAGTAGGGGGTGCCCAGGCAGGGGACGCA GTCTGGGCAAGGAAGGGACCGATCGGTACCGCTTGGTAGTAGGGGGTGCCCAGGCAGGGGACGCA T A IGSF8 Ensembl:ENSG00000162729 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160093801..160094108 26863196 MeRIP-seq:(Medium) rs1321989806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22751281 94158 RMVar_ID_94158 Human_SNP_ID_35901197 m1A Human chr1 - 160093851 160093851 160093851 GTCTGGGCAAGGAAGGGACCGATCGGTACCGCATGGTAGTAGGGGGTGCCCAGGCAGGGGACGCA GTCTGGGCAAGGAAGGGACCGATCGGTACCGCGTGGTAGTAGGGGGTGCCCAGGCAGGGGACGCA T C IGSF8 Ensembl:ENSG00000162729 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160093801..160094108 26863196 MeRIP-seq:(Medium) rs1321989806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22751281 94159 RMVar_ID_94159 Human_SNP_ID_35901351 m1A Human chr1 + 160094159 160094159 160094159 GGGGCCCTGGGGGGGCAGCAGACACCTGGAGGACATCTGGAAGAACTGGAGAGAACAGCTGGAGT GGGGCCCTGGGGGGGCAGCAGACACCTGGAGGTCATCTGGAAGAACTGGAGAGAACAGCTGGAGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:160094108..160095155 32194978 MeRIP-seq:(Medium) rs771004387 Functional Loss SNV dbSNP153 33..33 33 - - - 94160 RMVar_ID_94160 Human_SNP_ID_35902382 m1A Human chr1 + 160098531 160098531 160098531 CCGGGGGATGGCGCGGGTTCTGGGGGGCCGGAAGGGTGGGGGGCGCATGCCCAGGTTGAGGGCAG CCGGGGGATGGCGCGGGTTCTGGGGGGCCGGAGGGGTGGGGGGCGCATGCCCAGGTTGAGGGCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:160098451..160098625 26863410 MeRIP-seq:(Medium) rs1157663532 Functional Loss SNV dbSNP153 33..33 33 - - - 94161 RMVar_ID_94161 Human_SNP_ID_35931293 m1A Human chr1 + 160205485 160205485 160205485 GGTTCCGGACGCTGCTTAGGAACCGGGGACTCAGGAGTGCCCGCGCCCTGAGCGCTCAGCTCCAG GGTTCCGGACGCTGCTTAGGAACCGGGGACTCGGGAGTGCCCGCGCCCTGAGCGCTCAGCTCCAG A G PEA15 Ensembl:ENSG00000162734 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:160205448..160205547 26863410 MeRIP-seq:(Medium) rs1229404327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_971986,Human_RBP_ID_1413814,Human_RBP_ID_4001428,Human_RBP_ID_5413130,Human_RBP_ID_5484670 Human_Splice_Rec_147143,Human_Splice_Rec_147149,Human_Splice_Rec_147155 94162 RMVar_ID_94162 Human_SNP_ID_35931306 m1A Human chr1 - 160205524 160205524 160205524 TCCCCGCGACATGTCTCCTCTCCGCCCCTCTCACCGCCTCTGGAGCTGAGCGCTCAGGGCGCGGG TCCCCGCGACATGTCTCCTCTCCGCCCCTCTCTCCGCCTCTGGAGCTGAGCGCTCAGGGCGCGGG T A AL121987.2 Ensembl:ENSG00000227741 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:160205448..160205547;chr1:160205426..160205560 26863410 MeRIP-seq:(Medium) rs112457601 Functional Loss SNV dbSNP153 33..33 33 - - - 94163 RMVar_ID_94163 Human_SNP_ID_35931307 m1A Human chr1 - 160205524 160205524 160205524 TCCCCGCGACATGTCTCCTCTCCGCCCCTCTCACCGCCTCTGGAGCTGAGCGCTCAGGGCGCGGG TCCCCGCGACATGTCTCCTCTCCGCCCCTCTCGCCGCCTCTGGAGCTGAGCGCTCAGGGCGCGGG T C AL121987.2 Ensembl:ENSG00000227741 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:160205448..160205547;chr1:160205426..160205560 26863410 MeRIP-seq:(Medium) rs112457601 Functional Loss SNV dbSNP153 33..33 33 - - - 94164 RMVar_ID_94164 Human_SNP_ID_35931547 m1A Human chr1 - 160206515 160206515 160206515 CTCCATCCCTTGGCCACTCTTACCCAGAAACTAGCCACTCCCAGCACGCTAAGCCCTAACTGGAC CTCCATCCCTTGGCCACTCTTACCCAGAAACTGGCCACTCCCAGCACGCTAAGCCCTAACTGGAC T C AL121987.2 Ensembl:ENSG00000227741 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:160206512..160206766 26863196 MeRIP-seq:(Medium) rs935181345 Functional Loss SNV dbSNP153 33..33 33 - - - 94165 RMVar_ID_94165 Human_SNP_ID_35939299 m1A Human chr1 - 160239924 160239924 160239924 TCCCTGCCCTTCGGGAGCGGGAGCTGGGTTCAAGTGCCCGCTTTGTCTATGAGGCCTGTGGGGCA TCCCTGCCCTTCGGGAGCGGGAGCTGGGTTCAGGTGCCCGCTTTGTCTATGAGGCCTGTGGGGCA T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding CDS,3'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs763263130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413860,Human_RBP_ID_1727368,Human_RBP_ID_9357065 Human_miRNA_ID_2533740,Human_miRNA_ID_2535471 RMVar_hsa_circ_123319,RMVar_hsa_circ_137004,RMVar_hsa_circ_346799,RMVar_hsa_circ_109951,RMVar_hsa_circ_137005,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_267279,RMVar_hsa_circ_270197,RMVar_hsa_circ_137010,RMVar_hsa_circ_137009,RMVar_hsa_circ_125505,RMVar_hsa_circ_274375,RMVar_hsa_circ_340875,RMVar_hsa_circ_348906,RMVar_hsa_circ_341148,RMVar_hsa_circ_299355,RMVar_hsa_circ_137012,RMVar_hsa_circ_137013,RMVar_hsa_circ_344533,RMVar_hsa_circ_293177,RMVar_hsa_circ_61406,RMVar_hsa_circ_137015,RMVar_hsa_circ_137016,RMVar_hsa_circ_137014,RMVar_hsa_circ_327417,RMVar_hsa_circ_47567 94166 RMVar_ID_94166 Human_SNP_ID_35939333 m1A Human chr1 - 160240050 160240050 160240050 AGCCTCGGCGCCGTGTACAGCGCAAGCGGGCTAACCGTGACCAGGACTCATCAGATGATGAGCGG AGCCTCGGCGCCGTGTACAGCGCAAGCGGGCTGACCGTGACCAGGACTCATCAGATGATGAGCGG T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160240001..160240168 26863196 MeRIP-seq:(Medium) rs890486134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3934224,Human_RBP_ID_4001618,Human_RBP_ID_8228380,Human_RBP_ID_8736238,Human_RBP_ID_9357065,Human_RBP_ID_10614593,Human_RBP_ID_18410226,Human_RBP_ID_18415859,Human_RBP_ID_18966146,Human_RBP_ID_22026495,Human_RBP_ID_22870981,Human_RBP_ID_24358920,Human_RBP_ID_24541254,Human_RBP_ID_26309840,Human_RBP_ID_26844540,Human_RBP_ID_27798750 RMVar_hsa_circ_123319,RMVar_hsa_circ_137004,RMVar_hsa_circ_346799,RMVar_hsa_circ_109951,RMVar_hsa_circ_137005,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_267279,RMVar_hsa_circ_270197,RMVar_hsa_circ_137010,RMVar_hsa_circ_137009,RMVar_hsa_circ_125505,RMVar_hsa_circ_274375,RMVar_hsa_circ_340875,RMVar_hsa_circ_348906,RMVar_hsa_circ_341148,RMVar_hsa_circ_299355,RMVar_hsa_circ_137012,RMVar_hsa_circ_137013,RMVar_hsa_circ_344533,RMVar_hsa_circ_293177,RMVar_hsa_circ_61406,RMVar_hsa_circ_137015,RMVar_hsa_circ_137016,RMVar_hsa_circ_137014,RMVar_hsa_circ_327417,RMVar_hsa_circ_47567 94167 RMVar_ID_94167 Human_SNP_ID_35939437 m1A Human chr1 + 160240343 160240343 160240343 AGGATGTCTCCCTCCCCTCTTCAGCTCCAGACATCTCCTCTGGACTGCTAGACAGGCTTCCTGCA AGGATGTCTCCCTCCCCTCTTCAGCTCCAGACGTCTCCTCTGGACTGCTAGACAGGCTTCCTGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160240219..160261319 26863196 MeRIP-seq:(Medium) rs1443219783 Functional Loss SNV dbSNP153 33..33 33 - - - 94168 RMVar_ID_94168 Human_SNP_ID_35944756 m1A Human chr1 - 160262284 160262284 160262284 AACTGCCCCAGCCGGACACCCCCCCTCCCTTGACCTACCCGGTCTGTGTCTCGTTCCGGCTCGGC AACTGCCCCAGCCGGACACCCCCCCTCCCTTGGCCTACCCGGTCTGTGTCTCGTTCCGGCTCGGC T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:160262234..160262414 26863196 MeRIP-seq:(Medium) rs1356484261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074536,Human_RBP_ID_17072508,Human_RBP_ID_18928732 Human_Splice_Rec_147197,Human_Splice_Rec_147327,Human_Splice_Rec_147345 RMVar_hsa_circ_115602,RMVar_hsa_circ_137009 94169 RMVar_ID_94169 Human_SNP_ID_35952223 m1A Human chr1 - 160291348 160291348 160291348 TCGGCGCCTACTAGAACTCGGGCCCAAGCCTGAGGTGGCCCAACAGGTAGATGGAACTCCTTCAG TCGGCGCCTACTAGAACTCGGGCCCAAGCCTGCGGTGGCCCAACAGGTAGATGGAACTCCTTCAG T G COPA Ensembl:ENSG00000122218 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:160290169..160293175 32194978 MeRIP-seq:(Medium) rs748305561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_857448,Human_RBP_ID_8755202,Human_RBP_ID_9253000,Human_RBP_ID_9270418,Human_RBP_ID_17221677,Human_RBP_ID_17338502,Human_RBP_ID_26799068 Human_Splice_Rec_147601,Human_Splice_Rec_147663,Human_Splice_Rec_147715,Human_Splice_Rec_147779,Human_Splice_Rec_147839,Human_Splice_Rec_147899,Human_Splice_Rec_147963,Human_Splice_Rec_148023,Human_Splice_Rec_148087,Human_Splice_Rec_148109,Human_Splice_Rec_148173,Human_Splice_Rec_148233,Human_Splice_Rec_148285 RMVar_hsa_circ_83196,RMVar_hsa_circ_103491,RMVar_hsa_circ_137019,RMVar_hsa_circ_99830,RMVar_hsa_circ_137018,RMVar_hsa_circ_94259,RMVar_hsa_circ_137020,RMVar_hsa_circ_137021 94170 RMVar_ID_94170 Human_SNP_ID_35953590 m1A Human chr1 - 160297305 160297305 160297305 TATCCGAGACTTGCCAGCTTTTTCAGGGTCTGAGGAAGTATTTTTCTGTTTTTGTTGAGTTAATC TATCCGAGACTTGCCAGCTTTTTCAGGGTCTGGGGAAGTATTTTTCTGTTTTTGTTGAGTTAATC T C COPA Ensembl:ENSG00000122218 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160297301..160297389 26863196 MeRIP-seq:(Medium) rs1264785993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83196,RMVar_hsa_circ_99830,RMVar_hsa_circ_137018,RMVar_hsa_circ_5479,RMVar_hsa_circ_97035,RMVar_hsa_circ_94259,RMVar_hsa_circ_137020,RMVar_hsa_circ_137021,RMVar_hsa_circ_137024,RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_18002,RMVar_hsa_circ_137028,RMVar_hsa_circ_359528,RMVar_hsa_circ_363673,RMVar_hsa_circ_97323,RMVar_hsa_circ_102286,RMVar_hsa_circ_70148,RMVar_hsa_circ_118414,RMVar_hsa_circ_137030,RMVar_hsa_circ_71098,RMVar_hsa_circ_96707,RMVar_hsa_circ_62893,RMVar_hsa_circ_94232,RMVar_hsa_circ_137033,RMVar_hsa_circ_137032,RMVar_hsa_circ_74631,RMVar_hsa_circ_137035 94171 RMVar_ID_94171 Human_SNP_ID_35954012 m1A Human chr1 - 160299165 160299165 160299165 TACTGCCTAGACAGGGAGTGTCGTCCCCGGGTACTCACCATTGATCCCACTGAGTTCAAATTCAA TACTGCCTAGACAGGGAGTGTCGTCCCCGGGTGCTCACCATTGATCCCACTGAGTTCAAATTCAA T C COPA Ensembl:ENSG00000122218 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:160299114..160299264 32194978 MeRIP-seq:(Medium) rs1351815135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742364,Human_RBP_ID_8755222,Human_RBP_ID_9253029,Human_RBP_ID_9266520,Human_RBP_ID_17675407,Human_RBP_ID_17728155,Human_RBP_ID_18187831,Human_RBP_ID_18468632,Human_RBP_ID_19151802,Human_RBP_ID_22427648,Human_RBP_ID_22750321,Human_RBP_ID_26801185,Human_RBP_ID_27389986 Human_Splice_Rec_147574,Human_Splice_Rec_147575,Human_Splice_Rec_147636,Human_Splice_Rec_147637,Human_Splice_Rec_147690,Human_Splice_Rec_147691,Human_Splice_Rec_147752,Human_Splice_Rec_147753,Human_Splice_Rec_147872,Human_Splice_Rec_147873,Human_Splice_Rec_147936,Human_Splice_Rec_147937,Human_Splice_Rec_147996,Human_Splice_Rec_147997,Human_Splice_Rec_148060,Human_Splice_Rec_148061,Human_Splice_Rec_148146,Human_Splice_Rec_148147,Human_Splice_Rec_148258,Human_Splice_Rec_148259,Human_Splice_Rec_148289,Human_Splice_Rec_148324,Human_Splice_Rec_148325,Human_Splice_Rec_148344 Human_miRNA_ID_2149781 RMVar_hsa_circ_83196,RMVar_hsa_circ_99830,RMVar_hsa_circ_137018,RMVar_hsa_circ_30268,RMVar_hsa_circ_5479,RMVar_hsa_circ_97035,RMVar_hsa_circ_94259,RMVar_hsa_circ_137020,RMVar_hsa_circ_137021,RMVar_hsa_circ_137024,RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_137028,RMVar_hsa_circ_359528,RMVar_hsa_circ_363673,RMVar_hsa_circ_97323,RMVar_hsa_circ_102286,RMVar_hsa_circ_70148,RMVar_hsa_circ_118414,RMVar_hsa_circ_137030,RMVar_hsa_circ_71098,RMVar_hsa_circ_96707,RMVar_hsa_circ_62893,RMVar_hsa_circ_86396,RMVar_hsa_circ_94232,RMVar_hsa_circ_137033,RMVar_hsa_circ_137032,RMVar_hsa_circ_74631,RMVar_hsa_circ_137035,RMVar_hsa_circ_34001,RMVar_hsa_circ_88577,RMVar_hsa_circ_137036,RMVar_hsa_circ_326348,RMVar_hsa_circ_88509,RMVar_hsa_circ_86528,RMVar_hsa_circ_137038,RMVar_hsa_circ_137039,RMVar_hsa_circ_137037,RMVar_hsa_circ_82756,RMVar_hsa_circ_137040,RMVar_hsa_circ_137041 94172 RMVar_ID_94172 Human_SNP_ID_35957484 m1A Human chr1 + 160314028 160314028 160314028 GACATATCCCAGACTCGAATACTCTTGTCCTCAGAATTGCTGAGGATCAACTCTTGGCGAGGGTG GACATATCCCAGACTCGAATACTCTTGTCCTCCGAATTGCTGAGGATCAACTCTTGGCGAGGGTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:160313156..160332540 32194978 MeRIP-seq:(Medium) rs1316714607 Functional Loss SNV dbSNP153 33..33 33 - - - 94173 RMVar_ID_94173 Human_SNP_ID_35963335 m1A Human chr1 - 160338764 160338764 160338764 AAACAGTGATTCGAGGGGTTCGAGATGAACCAAGAGGGAGAAGAAGCCTCTTGGATGCCAAGGAA AAACAGTGATTCGAGGGGTTCGAGATGAACCAGGAGGGAGAAGAAGCCTCTTGGATGCCAAGGAA T C COPA Ensembl:ENSG00000122218 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:160338748..160338892 26863196 MeRIP-seq:(Medium) rs1046319162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_666,Human_RBP_ID_8940023 RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_88577,RMVar_hsa_circ_137039,RMVar_hsa_circ_81166,RMVar_hsa_circ_120443,RMVar_hsa_circ_137056,RMVar_hsa_circ_84740,RMVar_hsa_circ_137055,RMVar_hsa_circ_90612,RMVar_hsa_circ_137067,RMVar_hsa_circ_137068,RMVar_hsa_circ_82993,RMVar_hsa_circ_137069,RMVar_hsa_circ_15953 94174 RMVar_ID_94174 Human_SNP_ID_35963641 m1A Human chr1 + 160340214 160340214 160340214 ATCATGTTCATCAAACTTGTCAATGAGAGTGCACATCCGATAGTCCCATAACTGGATGACCCCAT ATCATGTTCATCAAACTTGTCAATGAGAGTGCGCATCCGATAGTCCCATAACTGGATGACCCCAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:160339966..160340300 32194978 MeRIP-seq:(Medium) rs200362589 Functional Loss SNV dbSNP153 33..33 33 - - - 94175 RMVar_ID_94175 Human_SNP_ID_35964284 m1A Human chr1 + 160343204 160343204 160343204 TCTCAGGTCTCCGACTCCGATGTCTTAATCCGAGCCCCGACACACCCTGCTGCCCTTCGGACGCC TCTCAGGTCTCCGACTCCGATGTCTTAATCCGGGCCCCGACACACCCTGCTGCCCTTCGGACGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr1:160343059..160343275;chr1:160340226..160343275;chr1:160343126..160343225 26863196 MeRIP-seq:(Medium) rs968665335 Functional Loss SNV dbSNP153 33..33 33 - - - 94176 RMVar_ID_94176 Human_SNP_ID_35964296 m1A Human chr1 - 160343219 160343219 160343219 GGTCGCTGACGTGGAGGCGTCCGAAGGGCAGCAGGGTGTGTCGGGGCTCGGATTAAGACATCGGA GGTCGCTGACGTGGAGGCGTCCGAAGGGCAGCGGGGTGTGTCGGGGCTCGGATTAAGACATCGGA T C COPA Ensembl:ENSG00000122218 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160343073..160343275 26863196 MeRIP-seq:(Medium) rs1292340368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19203,Human_RBP_ID_221664,Human_RBP_ID_741129,Human_RBP_ID_802384,Human_RBP_ID_4001921,Human_RBP_ID_5484680,Human_RBP_ID_8755248,Human_RBP_ID_9253071,Human_RBP_ID_9270467,Human_RBP_ID_22427663,Human_RBP_ID_23338153 Human_Splice_Rec_147541,Human_Splice_Rec_147605,Human_Splice_Rec_147719,Human_Splice_Rec_147783,Human_Splice_Rec_147843,Human_Splice_Rec_147903,Human_Splice_Rec_147967,Human_Splice_Rec_148027,Human_Splice_Rec_148113,Human_Splice_Rec_148177,Human_Splice_Rec_148349 Human_miRNA_ID_2428092,Human_miRNA_ID_2487891,Human_miRNA_ID_2510509,Human_miRNA_ID_2937149,Human_miRNA_ID_3053331 RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_81166,RMVar_hsa_circ_84740,RMVar_hsa_circ_137055,RMVar_hsa_circ_137068 94177 RMVar_ID_94177 Human_SNP_ID_35964420 m1A Human chr1 - 160343438 160343438 160343438 ACGCAGAAAGACAGAAGGCGAAGGAGACCCCGACTTCCCGGGTCAGCCCCAGAGCCACCCCCTGC ACGCAGAAAGACAGAAGGCGAAGGAGACCCCGGCTTCCCGGGTCAGCCCCAGAGCCACCCCCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:160343351..160343480 26863196 MeRIP-seq:(Medium) rs759140355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_81166,RMVar_hsa_circ_84740,RMVar_hsa_circ_137055,RMVar_hsa_circ_137068 94178 RMVar_ID_94178 Human_SNP_ID_35964426 m1A Human chr1 - 160343450 160343447 160343450 CCTGCTAGTAGGACGCAGAAAGACAGAAGGCGAAGGAGACCCCGACTTCCCGGGTCAGCCCCAGA CCTGCTAGTAGGACGCAGAAAGACAGAAGGCG___GAGACCCCGACTTCCCGGGTCAGCCCCAGA CCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:160343351..160343550 26863196 MeRIP-seq:(Medium) rs764980428 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_81166,RMVar_hsa_circ_84740,RMVar_hsa_circ_137055,RMVar_hsa_circ_137068 94179 RMVar_ID_94179 Human_SNP_ID_35964431 m1A Human chr1 - 160343450 160343450 160343450 CCTGCTAGTAGGACGCAGAAAGACAGAAGGCGAAGGAGACCCCGACTTCCCGGGTCAGCCCCAGA CCTGCTAGTAGGACGCAGAAAGACAGAAGGCGGAGGAGACCCCGACTTCCCGGGTCAGCCCCAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:160343351..160343550 26863196 MeRIP-seq:(Medium) rs141165822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_81166,RMVar_hsa_circ_84740,RMVar_hsa_circ_137055,RMVar_hsa_circ_137068 94180 RMVar_ID_94180 Human_SNP_ID_35978724 m1A Human chr1 - 160400654 160400653 160400654 CTTCCCCCTCAAGGCCCCGGGGGCTGGGGGCCAGGGGGGAATAGGGGGCGCTCAGGCTCCCATGG CTTCCCCCTCAAGGCCCCGGGGGCTGGGGGCC_GGGGGGAATAGGGGGCGCTCAGGCTCCCATGG CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:160400577..160400784 26863196 MeRIP-seq:(Medium) rs1204609723 Functional Loss DEL dbSNP153 33..33 33 - - - 94181 RMVar_ID_94181 Human_SNP_ID_36136815 m1A Human chr1 - 161021252 161021252 161021252 ACACCTGGCCGAGGTGACTCGTTCTGAAGAGCAGCGGTTCCTTACACCAATCGGAACGTGCAGGG ACACCTGGCCGAGGTGACTCGTTCTGAAGAGCTGCGGTTCCTTACACCAATCGGAACGTGCAGGG T A F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161021201..161021318 26863196 MeRIP-seq:(Medium) rs751009212 Functional Loss SNV dbSNP153 33..33 33 - - - 94182 RMVar_ID_94182 Human_SNP_ID_36136816 m1A Human chr1 - 161021252 161021252 161021252 ACACCTGGCCGAGGTGACTCGTTCTGAAGAGCAGCGGTTCCTTACACCAATCGGAACGTGCAGGG ACACCTGGCCGAGGTGACTCGTTCTGAAGAGCCGCGGTTCCTTACACCAATCGGAACGTGCAGGG T G F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161021201..161021318 26863196 MeRIP-seq:(Medium) rs751009212 Functional Loss SNV dbSNP153 33..33 33 - - - 94183 RMVar_ID_94183 Human_SNP_ID_36141137 m1A Human chr1 + 161037737 161037737 161037737 CCCGTTCACACCCTTAGTTAAGGTGGCCATTAAGGGGCCAGGGGGTGGCAATCAGTAAGCTGCCT CCCGTTCACACCCTTAGTTAAGGTGGCCATTACGGGGCCAGGGGGTGGCAATCAGTAAGCTGCCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:161037727..161037824 32194978 MeRIP-seq:(Medium) rs955077934 Functional Loss SNV dbSNP153 33..33 33 - - - 94184 RMVar_ID_94184 Human_SNP_ID_36141531 m1A Human chr1 + 161038918 161038918 161038918 CCATGGTGCGCGTAGCAACCGCGAGTCTCCGGAGTGCGGCCCTGGCCCGCCCTCTCGGCGCCTGC CCATGGTGCGCGTAGCAACCGCGAGTCTCCGGGGTGCGGCCCTGGCCCGCCCTCTCGGCGCCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:161038617..161038975;chr1:161038635..161038929;chr1:161038831..161038925 26863196 MeRIP-seq:(Medium) rs1050123696 Functional Loss SNV dbSNP153 33..33 33 - - - 94185 RMVar_ID_94185 Human_SNP_ID_36141795 m1A Human chr1 + 161039445 161039445 161039445 CAATCTCCTCTTCATGGGCACCAGCCACTGCTAAACATCCTTCCCTCACTTCTTGTGTAAGCTTG CAATCTCCTCTTCATGGGCACCAGCCACTGCTGAACATCCTTCCCTCACTTCTTGTGTAAGCTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161039394..161039463 26863196 MeRIP-seq:(Medium) rs1045682727 Functional Loss SNV dbSNP153 33..33 33 - - - 94186 RMVar_ID_94186 Human_SNP_ID_36143615 m1A Human chr1 + 161045863 161045863 161045863 CAGACTTCTGCCCGGTCCTACACTCACCGGCCAAGGCCGTCTCAGCTGCCGATTTTCTCCAACTG CAGACTTCTGCCCGGTCCTACACTCACCGGCCGAGGCCGTCTCAGCTGCCGATTTTCTCCAACTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161042629..161045927 26863196 MeRIP-seq:(Medium) rs907302946 Functional Loss SNV dbSNP153 33..33 33 - - - 94187 RMVar_ID_94187 Human_SNP_ID_36163203 m1A Human chr1 - 161117993 161117993 161117993 TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCTGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC T A PFDN2 Ensembl:ENSG00000143256 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161100614..161118075 26863196 MeRIP-seq:(Medium) rs781295624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20939,Human_RBP_ID_4083504,Human_RBP_ID_5136419,Human_RBP_ID_5311877,Human_RBP_ID_27801035 Human_Splice_Rec_149545,Human_Splice_Rec_149547 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 94188 RMVar_ID_94188 Human_SNP_ID_36163204 m1A Human chr1 - 161117993 161117993 161117993 TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCGGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC T C PFDN2 Ensembl:ENSG00000143256 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161100614..161118075 26863196 MeRIP-seq:(Medium) rs781295624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20939,Human_RBP_ID_4083504,Human_RBP_ID_5136419,Human_RBP_ID_5311877,Human_RBP_ID_27801035 Human_Splice_Rec_149545,Human_Splice_Rec_149547 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 94189 RMVar_ID_94189 Human_SNP_ID_36163205 m1A Human chr1 - 161117993 161117993 161117993 TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC TGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCCGCGGGAGCGGCGCGGGGAAGGGGGCGGTGTCC T G PFDN2 Ensembl:ENSG00000143256 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161100614..161118075 26863196 MeRIP-seq:(Medium) rs781295624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20939,Human_RBP_ID_4083504,Human_RBP_ID_5136419,Human_RBP_ID_5311877,Human_RBP_ID_27801035 Human_Splice_Rec_149545,Human_Splice_Rec_149547 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 94190 RMVar_ID_94190 Human_SNP_ID_36163210 m1A Human chr1 - 161117999 161117999 161117999 CGAAGATGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCG CGAAGATGGCGGAGAACAGCGGTCGCGCCGGCGAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCG T C PFDN2 Ensembl:ENSG00000143256 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:161102003..161118050;chr1:161100626..161118050 26863196 MeRIP-seq:(Medium) rs1292608687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20939,Human_RBP_ID_4083504,Human_RBP_ID_5136419 Human_Splice_Rec_149545,Human_Splice_Rec_149547 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 94191 RMVar_ID_94191 Human_SNP_ID_36163211 m1A Human chr1 - 161117999 161117999 161117999 CGAAGATGGCGGAGAACAGCGGTCGCGCCGGCAAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCG CGAAGATGGCGGAGAACAGCGGTCGCGCCGGCCAGAGCAGCGGGAGCGGCGCGGGGAAGGGGGCG T G PFDN2 Ensembl:ENSG00000143256 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:161102003..161118050;chr1:161100626..161118050 26863196 MeRIP-seq:(Medium) rs1292608687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20939,Human_RBP_ID_4083504,Human_RBP_ID_5136419 Human_Splice_Rec_149545,Human_Splice_Rec_149547 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 94192 RMVar_ID_94192 Human_SNP_ID_36163224 m1A Human chr1 + 161118009 161118009 161118009 CCCGCGCCGCTCCCGCTGCTCTTGCCGGCGCGACCGCTGTTCTCCGCCATCTTCGCCGCCTGCTG CCCGCGCCGCTCCCGCTGCTCTTGCCGGCGCGCCCGCTGTTCTCCGCCATCTTCGCCGCCTGCTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:161100626..161118050;chr1:161117893..161118025 26863196 MeRIP-seq:(Medium) rs1292581732 Functional Loss SNV dbSNP153 33..33 33 - - - 94193 RMVar_ID_94193 Human_SNP_ID_36163352 m1A Human chr1 + 161118169 161118169 161118169 CTCCGGATCGGACCCTGCGAATGGTTTTGGCTATATCTTCATGTAGGACCTACTCCCTATCCCGT CTCCGGATCGGACCCTGCGAATGGTTTTGGCTGTATCTTCATGTAGGACCTACTCCCTATCCCGT A G NIT1 Ensembl:ENSG00000158793 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:161118118..161118228 26863196 MeRIP-seq:(Medium) rs369706655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1250716,Human_RBP_ID_4074548,Human_RBP_ID_19039588 Human_Splice_Rec_149553,Human_Splice_Rec_149563,Human_Splice_Rec_149569,Human_Splice_Rec_149581,Human_Splice_Rec_149587,Human_Splice_Rec_149603,Human_Splice_Rec_149613,Human_Splice_Rec_149625,Human_Splice_Rec_149637,Human_Splice_Rec_149639 RMVar_hsa_circ_76659,RMVar_hsa_circ_137117,RMVar_hsa_circ_376402 94194 RMVar_ID_94194 Human_SNP_ID_36164230 m1A Human chr1 + 161120525 161120525 161120525 GCCCAGGTGTTGCTGCGGGCCCGTGCTATCGAAACCCAGTGCTATGTAGTGGCAGCAGCACAGTG GCCCAGGTGTTGCTGCGGGCCCGTGCTATCGACACCCAGTGCTATGTAGTGGCAGCAGCACAGTG A C NIT1 Ensembl:ENSG00000158793 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:161119508..161120534 32194978 MeRIP-seq:(Medium) rs1456915436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149580,Human_Splice_Rec_149602,Human_Splice_Rec_149624,Human_Splice_Rec_149652,Human_Splice_Rec_149666 94195 RMVar_ID_94195 Human_SNP_ID_36165464 m1A Human chr1 + 161124478 161124478 161124478 CGCTTTAGGCCCGCCATGCTGGGGGCTCAGGTACGCAATGCTTTCCAGAATCCCTGCTCAGCAGC CGCTTTAGGCCCGCCATGCTGGGGGCTCAGGTGCGCAATGCTTTCCAGAATCCCTGCTCAGCAGC A G NIT1 Ensembl:ENSG00000158793 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161124427..161131007 26863196 MeRIP-seq:(Medium) rs1276389611 Functional Loss SNV dbSNP153 33..33 33 - - - 94196 RMVar_ID_94196 Human_SNP_ID_36165470 m1A Human chr1 + 161124492 161124492 161124492 CATGCTGGGGGCTCAGGTACGCAATGCTTTCCAGAATCCCTGCTCAGCAGCTGCAATCCCCACCG CATGCTGGGGGCTCAGGTACGCAATGCTTTCCGGAATCCCTGCTCAGCAGCTGCAATCCCCACCG A G NIT1 Ensembl:ENSG00000158793 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161124442..161124556 26863196 MeRIP-seq:(Medium) rs1352889174 Functional Loss SNV dbSNP153 33..33 33 - - - 94197 RMVar_ID_94197 Human_SNP_ID_36166997 m1A Human chr1 + 161131444 161131444 161131444 TTAAAACAGCAAAAGGGTCTGGAAACTACAGCACTCATTTAATTAACCTGTCTAGATGCCACTCT TTAAAACAGCAAAAGGGTCTGGAAACTACAGCGCTCATTTAATTAACCTGTCTAGATGCCACTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161131442..161131619 26863196 MeRIP-seq:(Medium) rs1051965704 Functional Loss SNV dbSNP153 33..33 33 - - - 94198 RMVar_ID_94198 Human_SNP_ID_36167599 m1A Human chr1 + 161133570 161133570 161133570 GCCTGTGGAAGGGAGAGTGCGGATGGGGAGATACAGATTGGTTTAAGAGGTACGAATGTTGTGAC GCCTGTGGAAGGGAGAGTGCGGATGGGGAGATGCAGATTGGTTTAAGAGGTACGAATGTTGTGAC A G LOC112543491-001,LOC112543491-001:2 RNACentral:URS00008B5145,RNACentral:URS00008BFDC5 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161133520..161133586 26863196 MeRIP-seq:(Medium) rs1365546607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23338586 94199 RMVar_ID_94199 Human_SNP_ID_36172752 m1A Human chr1 - 161154026 161154026 161154026 CGGCGTTAGTCTTCAGCACCGGGATCTCAGACACAACACGTCGCGTGGCTTCATCCGCCATCTTG CGGCGTTAGTCTTCAGCACCGGGATCTCAGACGCAACACGTCGCGTGGCTTCATCCGCCATCTTG T C AL590714.1 Ensembl:ENSG00000224985 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:161153976..161157025;chr1:161153976..161154151 26863196 MeRIP-seq:(Medium) rs568476475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149826 94200 RMVar_ID_94200 Human_SNP_ID_36172756 m1A Human chr1 - 161154035 161154035 161154035 CTCGGGGTCCGGCGTTAGTCTTCAGCACCGGGATCTCAGACACAACACGTCGCGTGGCTTCATCC CTCGGGGTCCGGCGTTAGTCTTCAGCACCGGGTTCTCAGACACAACACGTCGCGTGGCTTCATCC T A AL590714.1 Ensembl:ENSG00000224985 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161153976..161154125 26863196 MeRIP-seq:(Medium) rs762935146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149826 94201 RMVar_ID_94201 Human_SNP_ID_36172757 m1A Human chr1 - 161154035 161154035 161154035 CTCGGGGTCCGGCGTTAGTCTTCAGCACCGGGATCTCAGACACAACACGTCGCGTGGCTTCATCC CTCGGGGTCCGGCGTTAGTCTTCAGCACCGGGCTCTCAGACACAACACGTCGCGTGGCTTCATCC T G AL590714.1 Ensembl:ENSG00000224985 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161153976..161154125 26863196 MeRIP-seq:(Medium) rs762935146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149826 94202 RMVar_ID_94202 Human_SNP_ID_36173851 m1A Human chr1 - 161158207 161158207 161158207 CCTTTTATGCCAAATACACAAAACTTACCCCCAGAGCCATGAGATGAGCTAGTCCAAATTTGGGC CCTTTTATGCCAAATACACAAAACTTACCCCCGGAGCCATGAGATGAGCTAGTCCAAATTTGGGC T C AL590714.1 Ensembl:ENSG00000224985 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:161158195..161158609 32194978 MeRIP-seq:(Medium) rs149244863 Functional Loss SNV dbSNP153 33..33 33 - - - 94203 RMVar_ID_94203 Human_SNP_ID_36174614 m1A Human chr1 - 161160795 161160795 161160795 GCCGTTCATCAGGCAGACCTGGCCGGGGAGGCAGAGGTCGTAACATGGGGTTTGGCCCAGAGGCT GCCGTTCATCAGGCAGACCTGGCCGGGGAGGCCGAGGTCGTAACATGGGGTTTGGCCCAGAGGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161160745..161160848 26863196 MeRIP-seq:(Medium) rs935089193 Functional Loss SNV dbSNP153 33..33 33 - - - 94204 RMVar_ID_94204 Human_SNP_ID_36174667 m1A Human chr1 + 161160919 161160919 161160919 CGAGCAGATCATGGGGTTCCCCTGCCTGGCTCACCACCCCCAACAGTGGCTTTGCCTCTCCCATC CGAGCAGATCATGGGGTTCCCCTGCCTGGCTCGCCACCCCCAACAGTGGCTTTGCCTCTCCCATC A G USP21 Ensembl:ENSG00000143258 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:161160813..161161042 26863196 MeRIP-seq:(Medium) rs370862481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149907 94205 RMVar_ID_94205 Human_SNP_ID_36179224 m1A Human chr1 - 161176076 161176076 161176076 TGCCTACCCCCAGAATTCCCCTCTCCCTCCCTAGATCTCACCCCCAGGATGTTGCGGAGGCTGCT TGCCTACCCCCAGAATTCCCCTCTCCCTCCCTGGATCTCACCCCCAGGATGTTGCGGAGGCTGCT T C B4GALT3 Ensembl:ENSG00000158850 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161176036..161176116 26863196 MeRIP-seq:(Medium) rs976733732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745271,Human_RBP_ID_5456521,Human_RBP_ID_5519246,Human_RBP_ID_9319230,Human_RBP_ID_18928746,Human_RBP_ID_24748842 Human_Splice_Rec_150302,Human_Splice_Rec_150316,Human_Splice_Rec_150354,Human_Splice_Rec_150360,Human_Splice_Rec_150368 94206 RMVar_ID_94206 Human_SNP_ID_36185163 m1A Human chr1 - 161198993 161198992 161198994 CATATGCACGAGAGAGACAGAGGAGGAAAGAGACAGAGACAAAGGCACAGCGGAAGAAGGCAGAG CATATGCACGAGAGAGACAGAGGAGGAAAGA__CAGAGACAAAGGCACAGCGGAAGAAGGCAGAG GTC G ADAMTS4 Ensembl:ENSG00000158859 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161198759..161199049 26863196 MeRIP-seq:(Medium) rs1031236266 Functional Loss DEL dbSNP153 32..33 33 - - - 94207 RMVar_ID_94207 Human_SNP_ID_36185925 m1A Human chr1 - 161202423 161202423 161202423 CTCCAGCCCCAGGCCGCAGCACCTGGGCCGCGACGCCCCGGAAGCCGCACAAAGCCCTCAGCGCC CTCCAGCCCCAGGCCGCAGCACCTGGGCCGCGGCGCCCCGGAAGCCGCACAAAGCCCTCAGCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:161202376..161202535;chr1:161202376..161202524;chr1:161202376..161203525;chr1:161202376..161203500 26863196 MeRIP-seq:(Medium) rs1396630476 Functional Loss SNV dbSNP153 33..33 33 - - - 94208 RMVar_ID_94208 Human_SNP_ID_36185967 m1A Human chr1 - 161202468 161202468 161202468 AGAGCTGCCCTCGATCTCACCTGCTGGGCTGAATCGGCAATCGGACTCCAGCCCCAGGCCGCAGC AGAGCTGCCCTCGATCTCACCTGCTGGGCTGAGTCGGCAATCGGACTCCAGCCCCAGGCCGCAGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:161202351..161202525 26863410 MeRIP-seq:(Medium) rs1405391267 Functional Loss SNV dbSNP153 33..33 33 - - - 94209 RMVar_ID_94209 Human_SNP_ID_36187611 m1A Human chr1 + 161209232 161209232 161209232 CATACTTTGACCGGCTAGACTATGTGTCCATGATGTGTAACGAACAGGCCTATTCTCTAGCTGTG CATACTTTGACCGGCTAGACTATGTGTCCATGGTGTGTAACGAACAGGCCTATTCTCTAGCTGTG A G NDUFS2 Ensembl:ENSG00000158864 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:161209218..161209600 32194978 MeRIP-seq:(Medium) rs765726842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1414014,Human_RBP_ID_1727522,Human_RBP_ID_9359535,Human_RBP_ID_18966185,Human_RBP_ID_22749561,Human_RBP_ID_23338697,Human_RBP_ID_26315870,Human_RBP_ID_26799103 Human_Splice_Rec_150412,Human_Splice_Rec_150420,Human_Splice_Rec_150421,Human_Splice_Rec_150446,Human_Splice_Rec_150447,Human_Splice_Rec_150454,Human_Splice_Rec_150455,Human_Splice_Rec_150480,Human_Splice_Rec_150481,Human_Splice_Rec_150498,Human_Splice_Rec_150499,Human_Splice_Rec_150506,Human_Splice_Rec_150507,Human_Splice_Rec_150509 Human_miRNA_ID_1978342,Human_miRNA_ID_1978343,Human_miRNA_ID_2275981,Human_miRNA_ID_2275982 RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_49463,RMVar_hsa_circ_88006,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_137139,RMVar_hsa_circ_120716,RMVar_hsa_circ_137140 94210 RMVar_ID_94210 Human_SNP_ID_36192691 m1A Human chr1 - 161226135 161226135 161226135 ACCAGGCCCGCAATGGTGCAGTATCCCTTACCATCTCAGACCATCATGCTGCCCCTTTCCCCCCG ACCAGGCCCGCAATGGTGCAGTATCCCTTACCGTCTCAGACCATCATGCTGCCCCTTTCCCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161226093..161226471 26863196 MeRIP-seq:(Medium) rs1315434073 Functional Loss SNV dbSNP153 33..33 33 - - - 94211 RMVar_ID_94211 Human_SNP_ID_36193418 m1A Human chr1 + 161228441 161228441 161228441 TGTACTTTGGATTTTACAGCTGTACACTGGGTAGCTACATTGAATGTGGGATCAGGCGGGGCCCA TGTACTTTGGATTTTACAGCTGTACACTGGGTGGCTACATTGAATGTGGGATCAGGCGGGGCCCA A G TOMM40L Ensembl:ENSG00000158882 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161228221..161228440 26863196 MeRIP-seq:(Medium) rs373013630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330309,Human_RBP_ID_5700365 Human_Splice_Rec_150650,Human_Splice_Rec_150651,Human_Splice_Rec_150662,Human_Splice_Rec_150663,Human_Splice_Rec_150680,Human_Splice_Rec_150681,Human_Splice_Rec_150698,Human_Splice_Rec_150699,Human_Splice_Rec_150720,Human_Splice_Rec_150721,Human_Splice_Rec_150736,Human_Splice_Rec_150737 94212 RMVar_ID_94212 Human_SNP_ID_36225688 m1A Human chr1 + 161356808 161356808 161356808 ACACAGCTAAGTTTGCACTTGTCTTCCCTCTCATGTATCATACCTGGAATGGGATCCGACACTTG ACACAGCTAAGTTTGCACTTGTCTTCCCTCTCGTGTATCATACCTGGAATGGGATCCGACACTTG A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs771059368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2098017,Human_RBP_ID_21879286,Human_RBP_ID_22749567 Human_Splice_Rec_151225,Human_Splice_Rec_151233,Human_Splice_Rec_151239,Human_Splice_Rec_151257,Human_Splice_Rec_151267 RMVar_hsa_circ_81462,RMVar_hsa_circ_301479,RMVar_hsa_circ_137157,RMVar_hsa_circ_137158 94213 RMVar_ID_94213 Human_SNP_ID_36227352 m1A Human chr1 - 161362823 161362823 161362823 ACAGGCAGTGGCACCCAAAGCCTCACCAACCCACCCCCCAACCCGGCCCATCCCCAGGGCAGAAG ACAGGCAGTGGCACCCAAAGCCTCACCAACCCCCCCCCCAACCCGGCCCATCCCCAGGGCAGAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:161362772..161362864;chr1:161362801..161362825 26863196 MeRIP-seq:(Medium) rs1036476854 Functional Loss SNV dbSNP153 33..33 33 - - - 94214 RMVar_ID_94214 Human_SNP_ID_36228301 m1A Human chr1 + 161366302 161366302 161366302 AGAGATGCTCTGGGGTACAAGTGGGAGAGATAAAGGTTTGTGAGGGGAAAAAGGGAAGTATTTGG AGAGATGCTCTGGGGTACAAGTGGGAGAGATACAGGTTTGTGAGGGGAAAAAGGGAAGTATTTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161366251..161366418 26863196 MeRIP-seq:(Medium) rs746780160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5700695 94215 RMVar_ID_94215 Human_SNP_ID_36228306 m1A Human chr1 + 161366317 161366317 161366317 TACAAGTGGGAGAGATAAAGGTTTGTGAGGGGAAAAAGGGAAGTATTTGGGGAGCTTGGTCAGAG TACAAGTGGGAGAGATAAAGGTTTGTGAGGGGGAAAAGGGAAGTATTTGGGGAGCTTGGTCAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161366227..161366418 26863196 MeRIP-seq:(Medium) rs201395829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5700698,Human_RBP_ID_18218212 94216 RMVar_ID_94216 Human_SNP_ID_36242540 m1A Human chr1 - 161422108 161422108 161422108 TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAAGTTTGCTTTTTTCCTTT TTCGGCGCTTTCACCGCCGCGGCCCGGGTTCGGTTCCCGGTCAGGGAAGTTTGCTTTTTTCCTTT T C AL592295.3 Ensembl:ENSG00000283360 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs922780616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330468,Human_RBP_ID_1439055,Human_RBP_ID_4077254,Human_RBP_ID_5161591,Human_RBP_ID_5254029,Human_RBP_ID_5273255,Human_RBP_ID_5484707,Human_RBP_ID_8288260,Human_RBP_ID_8957159,Human_RBP_ID_17675470,Human_RBP_ID_18554286,Human_RBP_ID_19208029,Human_RBP_ID_22780874,Human_RBP_ID_23121592,Human_RBP_ID_23338974,Human_RBP_ID_24455057 94217 RMVar_ID_94217 Human_SNP_ID_36242696 m1A Human chr1 - 161422257 161422257 161422257 GACCGTGGGGAGAGGGAGAGGGAGAAAAAGACATTCCTATAGGTTTCTAACATGTGCCTGAGGTG GACCGTGGGGAGAGGGAGAGGGAGAAAAAGACGTTCCTATAGGTTTCTAACATGTGCCTGAGGTG T C AL592295.3 Ensembl:ENSG00000283360 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161422207..161422314 26863196 MeRIP-seq:(Medium) rs1219735821 Functional Loss SNV dbSNP153 33..33 33 - - - 94218 RMVar_ID_94218 Human_SNP_ID_36242698 m1A Human chr1 - 161422262 161422260 161422262 AGGGAGACCGTGGGGAGAGGGAGAGGGAGAAAAAGACATTCCTATAGGTTTCTAACATGTGCCTG AGGGAGACCGTGGGGAGAGGGAGAGGGAGAAA__GACATTCCTATAGGTTTCTAACATGTGCCTG CTT C AL592295.3 Ensembl:ENSG00000283360 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161422212..161422314 26863196 MeRIP-seq:(Medium) rs141240282 Functional Loss DEL dbSNP153 33..34 33 - - - 94219 RMVar_ID_94219 Human_SNP_ID_36248042 m1A Human chr1 - 161440186 161440186 161440186 TAGTTGCCTTCCAAGCAGTTGACCCGGGCTCGATTCCCGCCCAACGCATCGGGCGGACCTTTTGC TAGTTGCCTTCCAAGCAGTTGACCCGGGCTCGGTTCCCGCCCAACGCATCGGGCGGACCTTTTGC T C AL592295.3,AL831711.1 Ensembl:ENSG00000283360,Ensembl:ENSG00000283317 lincRNA,lincRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1391444434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972097,Human_RBP_ID_1063848,Human_RBP_ID_1345146,Human_RBP_ID_1414086,Human_RBP_ID_5091305,Human_RBP_ID_5252897,Human_RBP_ID_5700887,Human_RBP_ID_8240260,Human_RBP_ID_8288270,Human_RBP_ID_8957163,Human_RBP_ID_10620128,Human_RBP_ID_17586710,Human_RBP_ID_17728529,Human_RBP_ID_18509851,Human_RBP_ID_18522667,Human_RBP_ID_18554296,Human_RBP_ID_21999654,Human_RBP_ID_22780878,Human_RBP_ID_23121600,Human_RBP_ID_23338984,Human_RBP_ID_24395625,Human_RBP_ID_24447911,Human_RBP_ID_26578802,Human_RBP_ID_27579989 94220 RMVar_ID_94220 Human_SNP_ID_36248200 m1A Human chr1 - 161440397 161440397 161440397 CGGGCGTAACGGGTCAGCCGCGCTGGCCTTGCACCGGTGGGGCGCGGGGCGGCCTTTGGAGAGGC CGGGCGTAACGGGTCAGCCGCGCTGGCCTTGCTCCGGTGGGGCGCGGGGCGGCCTTTGGAGAGGC T A AL592295.3,AL831711.1 Ensembl:ENSG00000283360,Ensembl:ENSG00000283317 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161440348..161440501 26863196 MeRIP-seq:(Medium) rs1461908323 Functional Loss SNV dbSNP153 33..33 33 - - - 94221 RMVar_ID_94221 Human_SNP_ID_36248201 m1A Human chr1 - 161440397 161440397 161440397 CGGGCGTAACGGGTCAGCCGCGCTGGCCTTGCACCGGTGGGGCGCGGGGCGGCCTTTGGAGAGGC CGGGCGTAACGGGTCAGCCGCGCTGGCCTTGCCCCGGTGGGGCGCGGGGCGGCCTTTGGAGAGGC T G AL592295.3,AL831711.1 Ensembl:ENSG00000283360,Ensembl:ENSG00000283317 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:161440348..161440501 26863196 MeRIP-seq:(Medium) rs1461908323 Functional Loss SNV dbSNP153 33..33 33 - - - 94222 RMVar_ID_94222 Human_SNP_ID_36248549 m1A Human chr1 - 161440840 161440840 161440840 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGCAGCCGTGCTTTTTGG TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGGCAGCCGTGCTTTTTGG T C AL592295.3,AL831711.1 Ensembl:ENSG00000283360,Ensembl:ENSG00000283317 lincRNA,lincRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1313291588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4077590,Human_RBP_ID_18205090,Human_RBP_ID_26747080 94223 RMVar_ID_94223 Human_SNP_ID_36264384 m1A Human chr1 - 161523862 161523862 161523862 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCAATGCACTTTCATTTTTTTCCGA TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGCTTCCCGGCCAATGCACTTTCATTTTTTTCCGA T G piR-33487,piR-33486,tRNA-Gly-GCC-2-1,piR-36173,TRG2,lnc-FCGR3A-2 RNACentral:URS000044CE8A,RNACentral:URS000044DA37,RNACentral:URS000013B42D,RNACentral:URS000043000B,RNACentral:URS00005AFD62,RNACentral:URS00008BD94B piRNA,piRNA,tRNA,piRNA,tRNA,lincRNA exon,exon,exon,exon,exon,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1237989509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330481,Human_RBP_ID_1414091,Human_RBP_ID_4077640,Human_RBP_ID_5252902,Human_RBP_ID_5273258,Human_RBP_ID_5456528,Human_RBP_ID_5544670,Human_RBP_ID_5700913,Human_RBP_ID_8240262,Human_RBP_ID_8288275,Human_RBP_ID_10620177,Human_RBP_ID_16970302,Human_RBP_ID_18174107,Human_RBP_ID_18508658,Human_RBP_ID_18554304,Human_RBP_ID_19029842,Human_RBP_ID_19208066,Human_RBP_ID_22780880,Human_RBP_ID_23112706,Human_RBP_ID_23121609,Human_RBP_ID_23303875,Human_RBP_ID_27152889,Human_RBP_ID_27390187 94224 RMVar_ID_94224 Human_SNP_ID_36264801 m1A Human chr1 - 161524559 161524559 161524559 CAGCAGTGAGGCTCTCCCTGCGGTTTCTCTGCAGCCAGCCCGGCTCGGATCTGCTCAGCTCCGCT CAGCAGTGAGGCTCTCCCTGCGGTTTCTCTGCCGCCAGCCCGGCTCGGATCTGCTCAGCTCCGCT T G lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161524335..161524625 26863196 MeRIP-seq:(Medium) rs425949 Functional Loss SNV dbSNP153 33..33 33 - - - 94225 RMVar_ID_94225 Human_SNP_ID_36265078 m1A Human chr1 - 161525121 161525121 161525121 GGCCCCCGCGTCCTTGGTGGCCTGGCGCTGCGAGTCATTGAAATAGGCGGGCACGGTGATCACTG GGCCCCCGCGTCCTTGGTGGCCTGGCGCTGCGCGTCATTGAAATAGGCGGGCACGGTGATCACTG T G lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161525071..161525309 26863196 MeRIP-seq:(Medium) rs1479069105 Functional Loss SNV dbSNP153 33..33 33 - - - 94226 RMVar_ID_94226 Human_SNP_ID_36265587 m1A Human chr1 + 161526241 161526241 161526241 GGAGAGGATGGTTCATGAAGCCGAGCAGTACAAGGCTGAGGATGAGGCCCAGAGGGACAGAGTGG GGAGAGGATGGTTCATGAAGCCGAGCAGTACAGGGCTGAGGATGAGGCCCAGAGGGACAGAGTGG A G AL590385.2,HSPA6 Ensembl:ENSG00000273112,Ensembl:ENSG00000173110 lincRNA,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161526130..161526281 26863196 MeRIP-seq:(Medium) rs570167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23302936 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94227 RMVar_ID_94227 Human_SNP_ID_36267246 m1A Human chr1 + 161531169 161531169 161531169 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCAAGGGTTTTTGTCTTTCC TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGTTTCCCGGCCAACGCAAGGGTTTTTGTCTTTCC A T lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1232154009 Functional Loss SNV dbSNP153 33..33 33 - - - 94228 RMVar_ID_94228 Human_SNP_ID_36267301 m1A Human chr1 - 161531190 161531190 161531190 TGAGAAAGGTTTTTCGTAGAAGGAAAGACAAAAACCCTTGCGTTGGCCGGGAATCGAACCCGGGT TGAGAAAGGTTTTTCGTAGAAGGAAAGACAAACACCCTTGCGTTGGCCGGGAATCGAACCCGGGT T G lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:161531089..161531275 26863196 MeRIP-seq:(Medium) rs1358799924 Functional Loss SNV dbSNP153 33..33 33 - - - 94229 RMVar_ID_94229 Human_SNP_ID_36267304 m1A Human chr1 - 161531193 161531193 161531193 GACTGAGAAAGGTTTTTCGTAGAAGGAAAGACAAAAACCCTTGCGTTGGCCGGGAATCGAACCCG GACTGAGAAAGGTTTTTCGTAGAAGGAAAGACGAAAACCCTTGCGTTGGCCGGGAATCGAACCCG T C lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:161531126..161531275 26863196 MeRIP-seq:(Medium) rs151017625 Functional Loss SNV dbSNP153 33..33 33 - - - 94230 RMVar_ID_94230 Human_SNP_ID_36267305 m1A Human chr1 - 161531195 161531195 161531195 CTGACTGAGAAAGGTTTTTCGTAGAAGGAAAGACAAAAACCCTTGCGTTGGCCGGGAATCGAACC CTGACTGAGAAAGGTTTTTCGTAGAAGGAAAGGCAAAAACCCTTGCGTTGGCCGGGAATCGAACC T C lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:161531150..161531223 26863196 MeRIP-seq:(Medium) rs543114875 Functional Loss SNV dbSNP153 33..33 33 - - - 94231 RMVar_ID_94231 Human_SNP_ID_36267330 m1A Human chr1 + 161531228 161531228 161531228 CTTTCCTTCTACGAAAAACCTTTCTCAGTCAGAACCTATAACGCGCTGTGTATCCGTTTTACGCC CTTTCCTTCTACGAAAAACCTTTCTCAGTCAGGACCTATAACGCGCTGTGTATCCGTTTTACGCC A G AL590385.2 Ensembl:ENSG00000273112 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr1:161531121..161531275;chr1:161531153..161531239 26863196 MeRIP-seq:(Medium) rs994289594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063847,Human_RBP_ID_1727571,Human_RBP_ID_5155776,Human_RBP_ID_5272929,Human_RBP_ID_5278590,Human_RBP_ID_5542091,Human_RBP_ID_9461297,Human_RBP_ID_10620190,Human_RBP_ID_18554317,Human_RBP_ID_19151834,Human_RBP_ID_22129975,Human_RBP_ID_22734842,Human_RBP_ID_22848825,Human_RBP_ID_23121624,Human_RBP_ID_24395629,Human_RBP_ID_24447913,Human_RBP_ID_26370497,Human_RBP_ID_26578804,Human_RBP_ID_27170457 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94232 RMVar_ID_94232 Human_SNP_ID_36267331 m1A Human chr1 + 161531228 161531228 161531228 CTTTCCTTCTACGAAAAACCTTTCTCAGTCAGAACCTATAACGCGCTGTGTATCCGTTTTACGCC CTTTCCTTCTACGAAAAACCTTTCTCAGTCAGTACCTATAACGCGCTGTGTATCCGTTTTACGCC A T AL590385.2 Ensembl:ENSG00000273112 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr1:161531121..161531275;chr1:161531153..161531239 26863196 MeRIP-seq:(Medium) rs994289594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063847,Human_RBP_ID_1727571,Human_RBP_ID_5155776,Human_RBP_ID_5272929,Human_RBP_ID_5278590,Human_RBP_ID_5542091,Human_RBP_ID_9461297,Human_RBP_ID_10620190,Human_RBP_ID_18554317,Human_RBP_ID_19151834,Human_RBP_ID_22129975,Human_RBP_ID_22734842,Human_RBP_ID_22848825,Human_RBP_ID_23121624,Human_RBP_ID_24395629,Human_RBP_ID_24447913,Human_RBP_ID_26370497,Human_RBP_ID_26578804,Human_RBP_ID_27170457 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94233 RMVar_ID_94233 Human_SNP_ID_36269978 m1A Human chr1 + 161540299 161540299 161540299 GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGATCCCACCCAGGGACGGAAGTCGCATTTTGTGA GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGGTCCCACCCAGGGACGGAAGTCGCATTTTGTGA A G lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs188147179 Functional Loss SNV dbSNP153 33..33 33 - - - 94234 RMVar_ID_94234 Human_SNP_ID_36269979 m1A Human chr1 + 161540299 161540299 161540299 GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGATCCCACCCAGGGACGGAAGTCGCATTTTGTGA GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGTTCCCACCCAGGGACGGAAGTCGCATTTTGTGA A T lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs188147179 Functional Loss SNV dbSNP153 33..33 33 - - - 94235 RMVar_ID_94235 Human_SNP_ID_36270021 m1A Human chr1 + 161540323 161540323 161540323 GTGGTTCGATCCCACCCAGGGACGGAAGTCGCATTTTGTGAACCCTGGGTTTTTGAAACTTTGAC GTGGTTCGATCCCACCCAGGGACGGAAGTCGCCTTTTGTGAACCCTGGGTTTTTGAAACTTTGAC A C AL590385.2 Ensembl:ENSG00000273112 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161540319..161540432 26863196 MeRIP-seq:(Medium) rs578140253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269113,Human_RBP_ID_330488,Human_RBP_ID_1414102,Human_RBP_ID_5272930,Human_RBP_ID_5456536,Human_RBP_ID_5484716,Human_RBP_ID_5700923,Human_RBP_ID_8288288,Human_RBP_ID_8957167,Human_RBP_ID_10620199,Human_RBP_ID_18554321,Human_RBP_ID_21908420,Human_RBP_ID_23121633,Human_RBP_ID_24529026,Human_RBP_ID_24598386,Human_RBP_ID_26753464,Human_RBP_ID_26767590 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94236 RMVar_ID_94236 Human_SNP_ID_36270022 m1A Human chr1 + 161540323 161540323 161540323 GTGGTTCGATCCCACCCAGGGACGGAAGTCGCATTTTGTGAACCCTGGGTTTTTGAAACTTTGAC GTGGTTCGATCCCACCCAGGGACGGAAGTCGCGTTTTGTGAACCCTGGGTTTTTGAAACTTTGAC A G AL590385.2 Ensembl:ENSG00000273112 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161540319..161540432 26863196 MeRIP-seq:(Medium) rs578140253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269113,Human_RBP_ID_330488,Human_RBP_ID_1414102,Human_RBP_ID_5272930,Human_RBP_ID_5456536,Human_RBP_ID_5484716,Human_RBP_ID_5700923,Human_RBP_ID_8288288,Human_RBP_ID_8957167,Human_RBP_ID_10620199,Human_RBP_ID_18554321,Human_RBP_ID_21908420,Human_RBP_ID_23121633,Human_RBP_ID_24529026,Human_RBP_ID_24598386,Human_RBP_ID_26753464,Human_RBP_ID_26767590 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94237 RMVar_ID_94237 Human_SNP_ID_36270023 m1A Human chr1 + 161540323 161540323 161540323 GTGGTTCGATCCCACCCAGGGACGGAAGTCGCATTTTGTGAACCCTGGGTTTTTGAAACTTTGAC GTGGTTCGATCCCACCCAGGGACGGAAGTCGCTTTTTGTGAACCCTGGGTTTTTGAAACTTTGAC A T AL590385.2 Ensembl:ENSG00000273112 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161540319..161540432 26863196 MeRIP-seq:(Medium) rs578140253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269113,Human_RBP_ID_330488,Human_RBP_ID_1414102,Human_RBP_ID_5272930,Human_RBP_ID_5456536,Human_RBP_ID_5484716,Human_RBP_ID_5700923,Human_RBP_ID_8288288,Human_RBP_ID_8957167,Human_RBP_ID_10620199,Human_RBP_ID_18554321,Human_RBP_ID_21908420,Human_RBP_ID_23121633,Human_RBP_ID_24529026,Human_RBP_ID_24598386,Human_RBP_ID_26753464,Human_RBP_ID_26767590 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 94238 RMVar_ID_94238 Human_SNP_ID_36287901 m1A Human chr1 + 161612774 161612774 161612774 CAGCTGCCTTTCAAGCAGTTAACGCGGGTTCGATTCCCGGGTAACGAAACGTTTTTGTCTTTCCT CAGCTGCCTTTCAAGCAGTTAACGCGGGTTCGGTTCCCGGGTAACGAAACGTTTTTGTCTTTCCT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1298371375 Functional Loss SNV dbSNP153 33..33 33 - - - 94239 RMVar_ID_94239 Human_SNP_ID_36321527 m1A Human chr1 - 161749944 161749944 161749944 CTGTTAGCACGGCCGTGATGCCCGCTTCCCTCAGGTGATCTGGCTCCGCGACGGCCGCGGCCCCA CTGTTAGCACGGCCGTGATGCCCGCTTCCCTCCGGTGATCTGGCTCCGCGACGGCCGCGGCCCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:161749801..161750075;chr1:161749801..161750019 26863196 MeRIP-seq:(Medium) rs752113173 Functional Loss SNV dbSNP153 33..33 33 - - - 94240 RMVar_ID_94240 Human_SNP_ID_36321570 m1A Human chr1 + 161750026 161750026 161750026 AGCTTCAAGGCGGGGCCTGGGGTCGAGGATCTATGGCGCCTCTTCGTGCCAGCGCTGGACAAACC AGCTTCAAGGCGGGGCCTGGGGTCGAGGATCTGTGGCGCCTCTTCGTGCCAGCGCTGGACAAACC A G DUSP12 Ensembl:ENSG00000081721 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161749806..161750025 26863196 MeRIP-seq:(Medium) rs1323041651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330513,Human_RBP_ID_4083720,Human_RBP_ID_17728563,Human_RBP_ID_22871866 Human_Splice_Rec_151825 RMVar_hsa_circ_88584,RMVar_hsa_circ_137165 94241 RMVar_ID_94241 Human_SNP_ID_36325577 m1A Human chr1 - 161766381 161766381 161766381 CCCGGGCTAAAAGGTGACTCCATGGTGCCGGCAACCCCAGCCGGCTCCCCCATTTCACAAGTTCC CCCGGGCTAAAAGGTGACTCCATGGTGCCGGCCACCCCAGCCGGCTCCCCCATTTCACAAGTTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161766299..161766465 26863196 MeRIP-seq:(Medium) rs760186881 Functional Loss SNV dbSNP153 33..33 33 - - - 94242 RMVar_ID_94242 Human_SNP_ID_36325584 m1A Human chr1 - 161766392 161766392 161766392 TGTGAAAGAGTCCCGGGCTAAAAGGTGACTCCATGGTGCCGGCAACCCCAGCCGGCTCCCCCATT TGTGAAAGAGTCCCGGGCTAAAAGGTGACTCCGTGGTGCCGGCAACCCCAGCCGGCTCCCCCATT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161766294..161778261 26863196 MeRIP-seq:(Medium) rs753909268 Functional Loss SNV dbSNP153 33..33 33 - - - 94243 RMVar_ID_94243 Human_SNP_ID_36368463 m1A Human chr1 - 161959345 161959345 161959345 AATGGAGCTATCTCCTCTCTCCAAACCCCACCACTGGCCCTTCCCTTACCCTTCTATTTTCTCAA AATGGAGCTATCTCCTCTCTCCAAACCCCACCGCTGGCCCTTCCCTTACCCTTCTATTTTCTCAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161959296..161959439 26863196 MeRIP-seq:(Medium) rs1283359505 Functional Loss SNV dbSNP153 33..33 33 - - - 94244 RMVar_ID_94244 Human_SNP_ID_36380073 m1A Human chr1 - 162006441 162006441 162006441 GAAGTGTCTAAAAACCTCACCAAGGAAAATGAACAAATCAAAGAGGACATGGAAGAAATTCGAAC GAAGTGTCTAAAAACCTCACCAAGGAAAATGAGCAAATCAAAGAGGACATGGAAGAAATTCGAAC T C OLFML2B Ensembl:ENSG00000162745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:162000300..162020088;chr1:162000300..162020137 26863196 MeRIP-seq:(Medium) rs374100255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_151878,Human_Splice_Rec_151894 RMVar_hsa_circ_29039,RMVar_hsa_circ_356635 94245 RMVar_ID_94245 Human_SNP_ID_36380078 m1A Human chr1 - 162006446 162006446 162006446 CTCAGGAAGTGTCTAAAAACCTCACCAAGGAAAATGAACAAATCAAAGAGGACATGGAAGAAATT CTCAGGAAGTGTCTAAAAACCTCACCAAGGAACATGAACAAATCAAAGAGGACATGGAAGAAATT T G OLFML2B Ensembl:ENSG00000162745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:162006395..162020137 26863196 MeRIP-seq:(Medium) rs1455988203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_151878,Human_Splice_Rec_151894 RMVar_hsa_circ_29039,RMVar_hsa_circ_356635 94246 RMVar_ID_94246 Human_SNP_ID_36380086 m1A Human chr1 - 162006460 162006460 162006460 TTTTTTTTTTCCTTCTCAGGAAGTGTCTAAAAACCTCACCAAGGAAAATGAACAAATCAAAGAGG TTTTTTTTTTCCTTCTCAGGAAGTGTCTAAAATCCTCACCAAGGAAAATGAACAAATCAAAGAGG T A OLFML2B Ensembl:ENSG00000162745 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:162006351..162006516 26863196 MeRIP-seq:(Medium) rs778563885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_151878,Human_Splice_Rec_151894 RMVar_hsa_circ_29039,RMVar_hsa_circ_356635 94247 RMVar_ID_94247 Human_SNP_ID_36384203 m1A Human chr1 + 162023759 162023759 162023759 CAGGAGGGCTCAGGTGGCTGGAAGGCGTTCGGACAGACGCCCGCGGTGCGCGCCGGGACGGGCGG CAGGAGGGCTCAGGTGGCTGGAAGGCGTTCGGGCAGACGCCCGCGGTGCGCGCCGGGACGGGCGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:162023714..162023845 26863196 MeRIP-seq:(Medium) rs114746071 Functional Loss SNV dbSNP153 33..33 33 - - - 94248 RMVar_ID_94248 Human_SNP_ID_36384226 m1A Human chr1 + 162023833 162023833 162023833 TCGGGACGCACGGGGACCGGACACGGGGAGGGAAGAGGCGGTGGCGGCGCGGGCTGCTGGGCGAG TCGGGACGCACGGGGACCGGACACGGGGAGGGTAGAGGCGGTGGCGGCGCGGGCTGCTGGGCGAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:162023655..162023882;chr1:162023539..162023870 26863196 MeRIP-seq:(Medium) rs540592535 Functional Loss SNV dbSNP153 33..33 33 - - - 94249 RMVar_ID_94249 Human_SNP_ID_36496656 m1A Human chr1 + 162497925 162497925 162497925 CCTCCCTGCGGAGCCGCTGGTCCGGCTGGCGGAGATGTGACCGCGGGCCCGGCCGGCCTGCCTCA CCTCCCTGCGGAGCCGCTGGTCCGGCTGGCGGGGATGTGACCGCGGGCCCGGCCGGCCTGCCTCA A G UHMK1 Ensembl:ENSG00000152332 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:162497874..162497953 26863196 MeRIP-seq:(Medium) rs1372887365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073127,Human_RBP_ID_18415861 94250 RMVar_ID_94250 Human_SNP_ID_36496699 m1A Human chr1 - 162498022 162498022 162498022 GGCCTCCAGAAAACGCGGCGGCTCCGCGCCCCAGGCGCAGCCGGATCCCGCCATCGGTGTGGGTT GGCCTCCAGAAAACGCGGCGGCTCCGCGCCCCGGGCGCAGCCGGATCCCGCCATCGGTGTGGGTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:162497976..162498050 26863196 MeRIP-seq:(Medium) rs1173273583 Functional Loss SNV dbSNP153 33..33 33 - - - 94251 RMVar_ID_94251 Human_SNP_ID_36512151 m1A Human chr1 + 162561702 162561702 162561702 CCGCGGCCCCCCGGATGAGGGTATATATTCGGAGCGAGCGCGGGACGCCGATGAGTGGCCGCGCG CCGCGGCCCCCCGGATGAGGGTATATATTCGGGGCGAGCGCGGGACGCCGATGAGTGGCCGCGCG A G UAP1 Ensembl:ENSG00000117143 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:162561601..162561825 26863410 MeRIP-seq:(Medium) rs1292557951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330839,Human_RBP_ID_4074562,Human_RBP_ID_5234047,Human_RBP_ID_5456549,Human_RBP_ID_5484736,Human_RBP_ID_8940190,Human_RBP_ID_23339769 Human_Splice_Rec_152067,Human_Splice_Rec_152087,Human_Splice_Rec_152105 RMVar_hsa_circ_137225,RMVar_hsa_circ_82328 94252 RMVar_ID_94252 Human_SNP_ID_36512161 m1A Human chr1 - 162561725 162561725 162561725 CTACGACCGTCTCCAGCTCCTTCCGCGCGGCCACTCATCGGCGTCCCGCGCTCGCTCCGAATATA CTACGACCGTCTCCAGCTCCTTCCGCGCGGCCCCTCATCGGCGTCCCGCGCTCGCTCCGAATATA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:162561676..162561775 32194978 MeRIP-seq:(Medium) rs541957300 Functional Loss SNV dbSNP153 33..33 33 - - - 94253 RMVar_ID_94253 Human_SNP_ID_36512252 m1A Human chr1 - 162562020 162562020 162562020 CATCCCTGGCCCCGCCATCCACCCGGCTGCCCAGCCCACACACCCTCTCGCGGGGTGGCGGAGGA CATCCCTGGCCCCGCCATCCACCCGGCTGCCCGGCCCACACACCCTCTCGCGGGGTGGCGGAGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:162562018..162562311 26863196 MeRIP-seq:(Medium) rs1402328124 Functional Loss SNV dbSNP153 33..33 33 - - - 94254 RMVar_ID_94254 Human_SNP_ID_36512267 m1A Human chr1 + 162562074 162562074 162562074 GGCCAGGGATGGAATGAGCGCGCCCCAGATGGACTGGGGGCGTTGTGGGAGGAGGTCTGGGCCAG GGCCAGGGATGGAATGAGCGCGCCCCAGATGGGCTGGGGGCGTTGTGGGAGGAGGTCTGGGCCAG A G UAP1 Ensembl:ENSG00000117143 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:162562027..162562260 26863196 MeRIP-seq:(Medium) rs1171275307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328690,Human_RBP_ID_9412087,Human_RBP_ID_23339770 RMVar_hsa_circ_137225,RMVar_hsa_circ_82328 94255 RMVar_ID_94255 Human_SNP_ID_36516953 m1A Human chr1 + 162581388 162581388 162581388 TTTGGAGCATTCATGTCTATTGTGTTGACAACATATTAGTAAAAGTGGCAGACCCACGGTTCATT TTTGGAGCATTCATGTCTATTGTGTTGACAACGTATTAGTAAAAGTGGCAGACCCACGGTTCATT A G UAP1 Ensembl:ENSG00000117143 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:162579537..162581425 32194978 MeRIP-seq:(Medium) rs753571677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8957353,Human_RBP_ID_26312117 Human_Splice_Rec_152075,Human_Splice_Rec_152095,Human_Splice_Rec_152113,Human_Splice_Rec_152131,Human_Splice_Rec_152143 Human_miRNA_ID_2454879 RMVar_hsa_circ_2024,RMVar_hsa_circ_286491,RMVar_hsa_circ_137225,RMVar_hsa_circ_82328,RMVar_hsa_circ_288800,RMVar_hsa_circ_340602,RMVar_hsa_circ_56796,RMVar_hsa_circ_103345,RMVar_hsa_circ_311274,RMVar_hsa_circ_137227,RMVar_hsa_circ_137228,RMVar_hsa_circ_338598,RMVar_hsa_circ_291971,RMVar_hsa_circ_304815,RMVar_hsa_circ_108581,RMVar_hsa_circ_137230,RMVar_hsa_circ_137232,RMVar_hsa_circ_69126,RMVar_hsa_circ_137233,RMVar_hsa_circ_137231,RMVar_hsa_circ_87439,RMVar_hsa_circ_137229,RMVar_hsa_circ_137234,RMVar_hsa_circ_6162 94256 RMVar_ID_94256 Human_SNP_ID_36516954 m1A Human chr1 + 162581388 162581388 162581388 TTTGGAGCATTCATGTCTATTGTGTTGACAACATATTAGTAAAAGTGGCAGACCCACGGTTCATT TTTGGAGCATTCATGTCTATTGTGTTGACAACTTATTAGTAAAAGTGGCAGACCCACGGTTCATT A T UAP1 Ensembl:ENSG00000117143 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:162579537..162581425 32194978 MeRIP-seq:(Medium) rs753571677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8957353,Human_RBP_ID_26312117 Human_Splice_Rec_152075,Human_Splice_Rec_152095,Human_Splice_Rec_152113,Human_Splice_Rec_152131,Human_Splice_Rec_152143 Human_miRNA_ID_2454879 RMVar_hsa_circ_2024,RMVar_hsa_circ_286491,RMVar_hsa_circ_137225,RMVar_hsa_circ_82328,RMVar_hsa_circ_288800,RMVar_hsa_circ_340602,RMVar_hsa_circ_56796,RMVar_hsa_circ_103345,RMVar_hsa_circ_311274,RMVar_hsa_circ_137227,RMVar_hsa_circ_137228,RMVar_hsa_circ_338598,RMVar_hsa_circ_291971,RMVar_hsa_circ_304815,RMVar_hsa_circ_108581,RMVar_hsa_circ_137230,RMVar_hsa_circ_137232,RMVar_hsa_circ_69126,RMVar_hsa_circ_137233,RMVar_hsa_circ_137231,RMVar_hsa_circ_87439,RMVar_hsa_circ_137229,RMVar_hsa_circ_137234,RMVar_hsa_circ_6162 94257 RMVar_ID_94257 Human_SNP_ID_36518375 m1A Human chr1 - 162587576 162587576 162587576 AACAGCAGTCGTCCGTCTGAGCTTCGTTTTTGAGCTGTTGCCAGGGAAATCTCACTATATTCTAC AACAGCAGTCGTCCGTCTGAGCTTCGTTTTTGGGCTGTTGCCAGGGAAATCTCACTATATTCTAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:162587526..162587684 32194978 MeRIP-seq:(Medium) rs377349247 Functional Loss SNV dbSNP153 33..33 33 - - - 94258 RMVar_ID_94258 Human_SNP_ID_36563765 m1A Human chr1 - 162780312 162780312 162780312 TTCATTAAATGTCCAGATGGAGTGGCATAGGCATGGGTGAGTGGTAGGTCTTGTAGGGAGGACCT TTCATTAAATGTCCAGATGGAGTGGCATAGGCGTGGGTGAGTGGTAGGTCTTGTAGGGAGGACCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:162780292..162780379 26863410 MeRIP-seq:(Medium) rs1281032817 Functional Loss SNV dbSNP153 33..33 33 - - - 94259 RMVar_ID_94259 Human_SNP_ID_36564696 m1A Human chr1 + 162784703 162784702 162784703 CAGTGGGGAATTGTTGAGTTGCTGTATCCTTTAAAAAAAAACAAAAAACTTGTTATTTTGAAAGA CAGTGGGGAATTGTTGAGTTGCTGTATCCTTT_AAAAAAAACAAAAAACTTGTTATTTTGAAAGA TA T DDR2 Ensembl:ENSG00000162733 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs887936133 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17729106 94260 RMVar_ID_94260 Human_SNP_ID_36564698 m1A Human chr1 + 162784703 162784703 162784703 CAGTGGGGAATTGTTGAGTTGCTGTATCCTTTAAAAAAAAACAAAAAACTTGTTATTTTGAAAGA CAGTGGGGAATTGTTGAGTTGCTGTATCCTTTTAAAAAAAACAAAAAACTTGTTATTTTGAAAGA A T DDR2 Ensembl:ENSG00000162733 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1302802921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17729106 94261 RMVar_ID_94261 Human_SNP_ID_36690210 m1A Human chr1 + 163312416 163312389 163312417 GATAGTAGTTATATGTAATGGGAGACTAAATAAAAGAAAGATCTGTATGAAGTGAAGTGGAAACT GATAGT____________________________AGAAAGATCTGTATGAAGTGAAGTGGAAACT TAGTTATATGTAATGGGAGACTAAATAAA T NUF2 Ensembl:ENSG00000143228 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:163312414..163312592 26863196 MeRIP-seq:(Medium) rs1442143681 Functional Loss DEL dbSNP153 7..34 33 - - - 94262 RMVar_ID_94262 Human_SNP_ID_36692354 m1A Human chr1 + 163321693 163321693 163321693 TTTCCTTCACTTGGTTTTGCTCTTCAACTCGGACCCCGAAAACGCTCTAAACGCTGGCGGAAGTC TTTCCTTCACTTGGTTTTGCTCTTCAACTCGGGCCCCGAAAACGCTCTAAACGCTGGCGGAAGTC A G NUF2 Ensembl:ENSG00000143228 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:163321644..163321719 26863196 MeRIP-seq:(Medium) rs961016754 Functional Loss SNV dbSNP153 33..33 33 - - - 94263 RMVar_ID_94263 Human_SNP_ID_36995894 m1A Human chr1 + 164559243 164559243 164559243 GCTGGAGTTTGCAGAGACACGGAGGAGGAGAGAGCCTGTGCTTTGCCTGCCGCCGCGGCTGGGGG GCTGGAGTTTGCAGAGACACGGAGGAGGAGAGGGCCTGTGCTTTGCCTGCCGCCGCGGCTGGGGG A G PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:164559193..164559335 26863196 MeRIP-seq:(Medium) rs1344877922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4084107 94264 RMVar_ID_94264 Human_SNP_ID_37024190 m1A Human chr1 + 164677610 164677610 164677610 ATGGGTTAAAAGTATAATGATATTTCAGAGACAAAAGCAGTGGTTTGGGGTTCATGAAAATTAAG ATGGGTTAAAAGTATAATGATATTTCAGAGACCAAAGCAGTGGTTTGGGGTTCATGAAAATTAAG A C PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:164677608..164677870 26863196 MeRIP-seq:(Medium) rs1557935676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41542,RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 94265 RMVar_ID_94265 Human_SNP_ID_37051259 m1A Human chr1 + 164792621 164792606 164792621 GAGAAGGGCGGAGGGTCGGCGGCAGCGGCGGCAGCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA GAGAAGGGCGGAGGGTCG_______________GCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA GGCGGCAGCGGCGGCA G PBX1 Ensembl:ENSG00000185630 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:164792462..164792700;chr1:164792504..164792675;chr1:164792476..164792700 26863196 MeRIP-seq:(Medium) rs1558010701 Functional Loss DEL dbSNP153 19..33 33 - - - Human_miRNA_ID_460487,Human_miRNA_ID_926101 RMVar_hsa_circ_41542,RMVar_hsa_circ_74927,RMVar_hsa_circ_329982,RMVar_hsa_circ_24162,RMVar_hsa_circ_324907,RMVar_hsa_circ_342573,RMVar_hsa_circ_291403,RMVar_hsa_circ_137264,RMVar_hsa_circ_137265,RMVar_hsa_circ_137263 94266 RMVar_ID_94266 Human_SNP_ID_37051270 m1A Human chr1 + 164792621 164792621 164792621 GAGAAGGGCGGAGGGTCGGCGGCAGCGGCGGCAGCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA GAGAAGGGCGGAGGGTCGGCGGCAGCGGCGGCGGCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA A G PBX1 Ensembl:ENSG00000185630 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:164792462..164792700;chr1:164792504..164792675;chr1:164792476..164792700 26863196 MeRIP-seq:(Medium) rs751176674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_460487,Human_miRNA_ID_926101 RMVar_hsa_circ_41542,RMVar_hsa_circ_74927,RMVar_hsa_circ_329982,RMVar_hsa_circ_24162,RMVar_hsa_circ_324907,RMVar_hsa_circ_342573,RMVar_hsa_circ_291403,RMVar_hsa_circ_137264,RMVar_hsa_circ_137265,RMVar_hsa_circ_137263 94267 RMVar_ID_94267 Human_SNP_ID_37051271 m1A Human chr1 + 164792621 164792621 164792621 GAGAAGGGCGGAGGGTCGGCGGCAGCGGCGGCAGCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA GAGAAGGGCGGAGGGTCGGCGGCAGCGGCGGCTGCGGCGGCGGCTTCTGGAGGGGCAGGTTCAGA A T PBX1 Ensembl:ENSG00000185630 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:164792462..164792700;chr1:164792504..164792675;chr1:164792476..164792700 26863196 MeRIP-seq:(Medium) rs751176674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_460487,Human_miRNA_ID_926101 RMVar_hsa_circ_41542,RMVar_hsa_circ_74927,RMVar_hsa_circ_329982,RMVar_hsa_circ_24162,RMVar_hsa_circ_324907,RMVar_hsa_circ_342573,RMVar_hsa_circ_291403,RMVar_hsa_circ_137264,RMVar_hsa_circ_137265,RMVar_hsa_circ_137263 94268 RMVar_ID_94268 Human_SNP_ID_417745522 m1A Human chr9 - 135119488 135119488 135119488 CCGTCCATGTACCACACCTGTGGAGAGAGCAGACCCGGTGGTGAGCACTTCCAAAGACCCAGTGA CCGTCCATGTACCACACCTGTGGAGAGAGCAGGCCCGGTGGTGAGCACTTCCAAAGACCCAGTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135119486..135119618 26863196 MeRIP-seq:(Medium) rs200592441 Functional Loss SNV dbSNP153 33..33 33 - - - 94269 RMVar_ID_94269 Human_SNP_ID_417745690 m1A Human chr9 + 135120001 135120001 135120001 GGCTACTCAGGGGGTACCAAGGTCCACTATGCATACCAGACCAATGCCTCCACCTATGAATACAT GGCTACTCAGGGGGTACCAAGGTCCACTATGCCTACCAGACCAATGCCTCCACCTATGAATACAT A C OLFM1 Ensembl:ENSG00000130558 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:135119976..135120000 26863196 MeRIP-seq:(Medium) rs956229703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27543897 94270 RMVar_ID_94270 Human_SNP_ID_417745691 m1A Human chr9 + 135120001 135120001 135120001 GGCTACTCAGGGGGTACCAAGGTCCACTATGCATACCAGACCAATGCCTCCACCTATGAATACAT GGCTACTCAGGGGGTACCAAGGTCCACTATGCTTACCAGACCAATGCCTCCACCTATGAATACAT A T OLFM1 Ensembl:ENSG00000130558 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:135119976..135120000 26863196 MeRIP-seq:(Medium) rs956229703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27543897 94271 RMVar_ID_94271 Human_SNP_ID_417754651 m1A Human chr9 + 135151548 135151548 135151548 GAGATTCCACTGCGTGATGGGCTCTTCCAGCCACCATAGTACCCAAGCCACAGGGACCAGATTCA GAGATTCCACTGCGTGATGGGCTCTTCCAGCCCCCATAGTACCCAAGCCACAGGGACCAGATTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135151515..135151809 26863196 MeRIP-seq:(Medium) rs911953416 Functional Loss SNV dbSNP153 33..33 33 - - - 94272 RMVar_ID_94272 Human_SNP_ID_417784415 m1A Human chr9 - 135253808 135253808 135253808 CGGCGATCCCGCTGTGGCCAGGCAGACGACGCAGGAGCTGAGGGCTGCCCGACGGCACGGCAGCA CGGCGATCCCGCTGTGGCCAGGCAGACGACGCGGGAGCTGAGGGCTGCCCGACGGCACGGCAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135253770..135253887 26863196 MeRIP-seq:(Medium) rs947962931 Functional Loss SNV dbSNP153 33..33 33 - - - 94273 RMVar_ID_94273 Human_SNP_ID_417845609 m1A Human chr9 - 135467044 135467044 135467044 CAGACTAAACTGTCATGTTTAAAGATAGAGATATTAAATAATTTGACCTAAATGAAAGTGTAGAG CAGACTAAACTGTCATGTTTAAAGATAGAGATGTTAAATAATTTGACCTAAATGAAAGTGTAGAG T C PPP1R26-AS1 Ensembl:ENSG00000225361 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:135466995..135467090 26863196 MeRIP-seq:(Medium) rs1450308288 Functional Loss SNV dbSNP153 33..33 33 - - - 94274 RMVar_ID_94274 Human_SNP_ID_417848863 m1A Human chr9 - 135479152 135479152 135479152 GGGGCGGCGGCTCCTCGAGCACACCTGCCGCCAGGTTCGGGGGAGGGAACAGTTTCTAGGAACTG GGGGCGGCGGCTCCTCGAGCACACCTGCCGCCGGGTTCGGGGGAGGGAACAGTTTCTAGGAACTG T C PPP1R26-AS1 Ensembl:ENSG00000225361 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:135479103..135479240 26863196 MeRIP-seq:(Medium) rs1402586619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8226110,Human_RBP_ID_8276052 94275 RMVar_ID_94275 Human_SNP_ID_417849175 m1A Human chr9 - 135479957 135479957 135479957 CCCGCCTGCGCCCGCGTCCCACGTCCCGGGGGAGGCGGCGGGCCGGGGGCGGGCCGGAGGCTGCA CCCGCCTGCGCCCGCGTCCCACGTCCCGGGGGGGGCGGCGGGCCGGGGGCGGGCCGGAGGCTGCA T C PPP1R26-AS1 Ensembl:ENSG00000225361 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr9:135479905..135480159;chr9:135479851..135480000 26863410 MeRIP-seq:(Medium) rs926229380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26796815 94276 RMVar_ID_94276 Human_SNP_ID_417850002 m1A Human chr9 + 135482706 135482706 135482706 TTCTGGTAGTCAAAAGTCTATTGAAAAAGCAGAGAGAGAATGCCTCGGTGTGTAAGTGGAGTGAT TTCTGGTAGTCAAAAGTCTATTGAAAAAGCAGGGAGAGAATGCCTCGGTGTGTAAGTGGAGTGAT A G PPP1R26 Ensembl:ENSG00000196422 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:135479847..135482756 26863196 MeRIP-seq:(Medium) rs190880880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964123,Human_RBP_ID_5018340,Human_RBP_ID_24292015 Human_Splice_Rec_1097476,Human_Splice_Rec_1097486,Human_Splice_Rec_1097494 RMVar_hsa_circ_113515,RMVar_hsa_circ_54160,RMVar_hsa_circ_260770 94277 RMVar_ID_94277 Human_SNP_ID_417850007 m1A Human chr9 + 135482733 135482733 135482733 AGCAGAGAGAGAATGCCTCGGTGTGTAAGTGGAGTGATGAGGACCTGATCTCTGGGCCGTGTGGG AGCAGAGAGAGAATGCCTCGGTGTGTAAGTGGTGTGATGAGGACCTGATCTCTGGGCCGTGTGGG A T PPP1R26 Ensembl:ENSG00000196422 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135482667..135482772 26863196 MeRIP-seq:(Medium) rs1172726903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24292015 Human_Splice_Rec_1097476,Human_Splice_Rec_1097477,Human_Splice_Rec_1097486,Human_Splice_Rec_1097487,Human_Splice_Rec_1097494,Human_Splice_Rec_1097495,Human_Splice_Rec_1097499 RMVar_hsa_circ_113515,RMVar_hsa_circ_54160,RMVar_hsa_circ_260770 94278 RMVar_ID_94278 Human_SNP_ID_417850901 m1A Human chr9 + 135485503 135485503 135485503 CCGGCAACCCCCTGCCGCCCTTCAGAAGCAGCACAGAATAAAGGTGGGATCAAAAGGAGCGCCAG CCGGCAACCCCCTGCCGCCCTTCAGAAGCAGCGCAGAATAAAGGTGGGATCAAAAGGAGCGCCAG A G PPP1R26 Ensembl:ENSG00000196422 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:135485452..135485633 26863196 MeRIP-seq:(Medium) rs765781609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113515,RMVar_hsa_circ_260770,RMVar_hsa_circ_123719,RMVar_hsa_circ_260771 94279 RMVar_ID_94279 Human_SNP_ID_417850916 m1A Human chr9 + 135485542 135485542 135485542 AAAGGTGGGATCAAAAGGAGCGCCAGCGCTGCAAGGAGGGGAAAGCGAGTCATGAGTGCGGCACA AAAGGTGGGATCAAAAGGAGCGCCAGCGCTGCCAGGAGGGGAAAGCGAGTCATGAGTGCGGCACA A C PPP1R26 Ensembl:ENSG00000196422 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135485491..135485636 26863196 MeRIP-seq:(Medium) rs1295858482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22733165,Human_RBP_ID_27132981 RMVar_hsa_circ_113515,RMVar_hsa_circ_260770,RMVar_hsa_circ_123719,RMVar_hsa_circ_260771 94280 RMVar_ID_94280 Human_SNP_ID_417850921 m1A Human chr9 - 135485559 135485559 135485559 CGGACGCCTCGGACGCCTGTGCCGCACTCATGACTCGCTTTCCCCTCCTTGCAGCGCTGGCGCTC CGGACGCCTCGGACGCCTGTGCCGCACTCATGGCTCGCTTTCCCCTCCTTGCAGCGCTGGCGCTC T C lnc-GLT6D1-2 RNACentral:URS00008B66B3 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:135485553..135485719 26863196 MeRIP-seq:(Medium) rs771713276 Functional Loss SNV dbSNP153 33..33 33 - - - 94281 RMVar_ID_94281 Human_SNP_ID_417855780 m1A Human chr9 - 135500755 135500755 135500755 GCTCCTCCCCAGGGTCCCGCAAGCGCGCGCTCACCCGCGCCGAGTATTCGGGGCAGCGCGGCCGA GCTCCTCCCCAGGGTCCCGCAAGCGCGCGCTCTCCCGCGCCGAGTATTCGGGGCAGCGCGGCCGA T A C9orf116 Ensembl:ENSG00000160345 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:135500750..135500889;chr9:135500731..135500982 26863196 MeRIP-seq:(Medium) rs774077286 Functional Loss SNV dbSNP153 33..33 33 - - - 94282 RMVar_ID_94282 Human_SNP_ID_417855931 m1A Human chr9 + 135501042 135501042 135501042 CGTCGCGCTGGTTGGGCTTTCTCGGGAAGGCGACCCCCCGGCCTGCTCGGCCGAGCCGCAGGACG CGTCGCGCTGGTTGGGCTTTCTCGGGAAGGCGCCCCCCCGGCCTGCTCGGCCGAGCCGCAGGACG A C MRPS2 Ensembl:ENSG00000122140 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:135500651..135501150 26863410 MeRIP-seq:(Medium) rs756128845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036567,Human_RBP_ID_19147842 Human_Splice_Rec_1097530,Human_Splice_Rec_1097531,Human_Splice_Rec_1097536,Human_Splice_Rec_1097537,Human_Splice_Rec_1097542,Human_Splice_Rec_1097543,Human_Splice_Rec_1097550,Human_Splice_Rec_1097551,Human_Splice_Rec_1097558,Human_Splice_Rec_1097564,Human_Splice_Rec_1097565,Human_Splice_Rec_1097569 RMVar_hsa_circ_67977,RMVar_hsa_circ_124833,RMVar_hsa_circ_82747,RMVar_hsa_circ_260773,RMVar_hsa_circ_260774 94283 RMVar_ID_94283 Human_SNP_ID_417855932 m1A Human chr9 + 135501042 135501042 135501042 CGTCGCGCTGGTTGGGCTTTCTCGGGAAGGCGACCCCCCGGCCTGCTCGGCCGAGCCGCAGGACG CGTCGCGCTGGTTGGGCTTTCTCGGGAAGGCGTCCCCCCGGCCTGCTCGGCCGAGCCGCAGGACG A T MRPS2 Ensembl:ENSG00000122140 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:135500651..135501150 26863410 MeRIP-seq:(Medium) rs756128845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036567,Human_RBP_ID_19147842 Human_Splice_Rec_1097530,Human_Splice_Rec_1097531,Human_Splice_Rec_1097536,Human_Splice_Rec_1097537,Human_Splice_Rec_1097542,Human_Splice_Rec_1097543,Human_Splice_Rec_1097550,Human_Splice_Rec_1097551,Human_Splice_Rec_1097558,Human_Splice_Rec_1097564,Human_Splice_Rec_1097565,Human_Splice_Rec_1097569 RMVar_hsa_circ_67977,RMVar_hsa_circ_124833,RMVar_hsa_circ_82747,RMVar_hsa_circ_260773,RMVar_hsa_circ_260774 94284 RMVar_ID_94284 Human_SNP_ID_417857119 m1A Human chr9 - 135504400 135504400 135504400 CAGGGACAGCAGCATCTTCTAGCAGCTTGGCCATACCAGCCACTGAGGTCCTAACTGCAGCCAAG CAGGGACAGCAGCATCTTCTAGCAGCTTGGCCGTACCAGCCACTGAGGTCCTAACTGCAGCCAAG T C AL161452.1 Ensembl:ENSG00000226706 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:135504351..135504500 32194978 MeRIP-seq:(Medium) rs1473511073 Functional Loss SNV dbSNP153 33..33 33 - - - 94285 RMVar_ID_94285 Human_SNP_ID_417953711 m1A Human chr9 + 135821341 135821341 135821341 AGGAGCCCTGTGGCCTGTCTTTTGGGACCTTCAGCTCCGCCGGCCTTCCGGAACGGGAATTCCGG AGGAGCCCTGTGGCCTGTCTTTTGGGACCTTCTGCTCCGCCGGCCTTCCGGAACGGGAATTCCGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:135821241..135821492 32194978 MeRIP-seq:(Medium) rs1196595794 Functional Loss SNV dbSNP153 33..33 33 - - - 94286 RMVar_ID_94286 Human_SNP_ID_417957972 m1A Human chr9 + 135836457 135836457 135836457 CGTCACCACACACTTTCTACCCTGTTCTACAGACACGTCACCACACACTTTCTACCCTGTTCTAC CGTCACCACACACTTTCTACCCTGTTCTACAGGCACGTCACCACACACTTTCTACCCTGTTCTAC A G NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135836433..135836514 26863196 MeRIP-seq:(Medium) rs1384800228 Functional Loss SNV dbSNP153 33..33 33 - - - 94287 RMVar_ID_94287 Human_SNP_ID_417957993 m1A Human chr9 + 135836563 135836528 135836563 CACAGTCATGTACCTTCTACCCCGTTCTACAGACACACATCACCACACACTTTCTACCCATTCTG _________________________________CACACATCACCACACACTTTCTACCCATTCTG CCACACAGTCATGTACCTTCTACCCCGTTCTACAGA C NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135836188..135837093 26863196 MeRIP-seq:(Medium) rs1564429986 Functional Loss DEL dbSNP153 1..33 33 - - - 94288 RMVar_ID_94288 Human_SNP_ID_417958008 m1A Human chr9 + 135836561 135836561 135836561 CACACAGTCATGTACCTTCTACCCCGTTCTACAGACACACATCACCACACACTTTCTACCCATTC CACACAGTCATGTACCTTCTACCCCGTTCTACGGACACACATCACCACACACTTTCTACCCATTC A G NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:135836418..135836748 26863196 MeRIP-seq:(Medium) rs935140383 Functional Loss SNV dbSNP153 33..33 33 - - - 94289 RMVar_ID_94289 Human_SNP_ID_417958009 m1A Human chr9 + 135836563 135836563 135836563 CACAGTCATGTACCTTCTACCCCGTTCTACAGACACACATCACCACACACTTTCTACCCATTCTG CACAGTCATGTACCTTCTACCCCGTTCTACAGGCACACATCACCACACACTTTCTACCCATTCTG A G NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135836188..135837093 26863196 MeRIP-seq:(Medium) rs1158374662 Functional Loss SNV dbSNP153 33..33 33 - - - 94290 RMVar_ID_94290 Human_SNP_ID_417958087 m1A Human chr9 + 135836736 135836736 135836736 TACAGACACACATCACCACGCACTTTCTACCCATTCCACAGCCACACATTGTCACGTACCTTCTA TACAGACACACATCACCACGCACTTTCTACCCCTTCCACAGCCACACATTGTCACGTACCTTCTA A C NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135836711..135836803 26863196 MeRIP-seq:(Medium) rs58282610 Functional Loss SNV dbSNP153 33..33 33 - - - 94291 RMVar_ID_94291 Human_SNP_ID_417958088 m1A Human chr9 + 135836736 135836736 135836736 TACAGACACACATCACCACGCACTTTCTACCCATTCCACAGCCACACATTGTCACGTACCTTCTA TACAGACACACATCACCACGCACTTTCTACCCGTTCCACAGCCACACATTGTCACGTACCTTCTA A G NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135836711..135836803 26863196 MeRIP-seq:(Medium) rs58282610 Functional Loss SNV dbSNP153 33..33 33 - - - 94292 RMVar_ID_94292 Human_SNP_ID_417958274 m1A Human chr9 + 135837205 135837205 135837205 ACATCATCACGCACTTTCTACCCATTCCAGAGACACACGTCACCACGGACATTCTACAGACACAC ACATCATCACGCACTTTCTACCCATTCCAGAGGCACACGTCACCACGGACATTCTACAGACACAC A G NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135837179..135837297 26863196 MeRIP-seq:(Medium) rs976196139 Functional Loss SNV dbSNP153 33..33 33 - - - 94293 RMVar_ID_94293 Human_SNP_ID_417958754 m1A Human chr9 + 135838197 135838195 135838197 ACTTTCCACCCGTTCTACAGACACACGTCATCACACACTTTCCACCCGTTCTACAGACACACGTC ACTTTCCACCCGTTCTACAGACACACGTCAT__CACACTTTCCACCCGTTCTACAGACACACGTC TCA T NONHSAG053777.2 RNACentral:URS00009BB400 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135837858..135839108 26863196 MeRIP-seq:(Medium) rs1191704960 Functional Loss DEL dbSNP153 32..33 33 - - - 94294 RMVar_ID_94294 Human_SNP_ID_417958899 m1A Human chr9 - 135838522 135838522 135838522 CATGATGATGTGTGTCTGTAGAATGGGTGGAAAGTGCGTGATGACGTGTGTCTGTAGAAGGGGTA CATGATGATGTGTGTCTGTAGAATGGGTGGAACGTGCGTGATGACGTGTGTCTGTAGAAGGGGTA T G CAMSAP1 Ensembl:ENSG00000130559 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135838477..135838598 26863196 MeRIP-seq:(Medium) rs985585701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24292153 RMVar_hsa_circ_34745,RMVar_hsa_circ_91970,RMVar_hsa_circ_342118,RMVar_hsa_circ_105500,RMVar_hsa_circ_83068,RMVar_hsa_circ_260777,RMVar_hsa_circ_260778,RMVar_hsa_circ_99970,RMVar_hsa_circ_260780,RMVar_hsa_circ_94018,RMVar_hsa_circ_78142,RMVar_hsa_circ_125052,RMVar_hsa_circ_260781,RMVar_hsa_circ_260782,RMVar_hsa_circ_260783,RMVar_hsa_circ_103605,RMVar_hsa_circ_322971,RMVar_hsa_circ_260785,RMVar_hsa_circ_260786,RMVar_hsa_circ_372783,RMVar_hsa_circ_260788,RMVar_hsa_circ_111726,RMVar_hsa_circ_260789,RMVar_hsa_circ_338388,RMVar_hsa_circ_260790 94295 RMVar_ID_94295 Human_SNP_ID_417977818 m1A Human chr9 + 135907344 135907344 135907344 GCCGCCGCCGTCGCCGCCCCCGCGGCTGCTGCATGCTGCGGGCGCTGAGCCCGAGCGGAGGAGGT GCCGCCGCCGTCGCCGCCCCCGCGGCTGCTGCGTGCTGCGGGCGCTGAGCCCGAGCGGAGGAGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135907053..135907505 26863196 MeRIP-seq:(Medium) rs1177178241 Functional Loss SNV dbSNP153 33..33 33 - - - 94296 RMVar_ID_94296 Human_SNP_ID_417977819 m1A Human chr9 + 135907344 135907344 135907344 GCCGCCGCCGTCGCCGCCCCCGCGGCTGCTGCATGCTGCGGGCGCTGAGCCCGAGCGGAGGAGGT GCCGCCGCCGTCGCCGCCCCCGCGGCTGCTGCTTGCTGCGGGCGCTGAGCCCGAGCGGAGGAGGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135907053..135907505 26863196 MeRIP-seq:(Medium) rs1177178241 Functional Loss SNV dbSNP153 33..33 33 - - - 94297 RMVar_ID_94297 Human_SNP_ID_417978400 m1A Human chr9 - 135908754 135908754 135908754 TCGACGCCCACGTCCCGCCGGTCTTTGCTCAAATAAGTGCCCTCCTCCTATGGCTTTCCTTGACC TCGACGCCCACGTCCCGCCGGTCTTTGCTCAATTAAGTGCCCTCCTCCTATGGCTTTCCTTGACC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135908707..135908897 26863196 MeRIP-seq:(Medium) rs763362785 Functional Loss SNV dbSNP153 33..33 33 - - - 94298 RMVar_ID_94298 Human_SNP_ID_417978401 m1A Human chr9 - 135908754 135908754 135908754 TCGACGCCCACGTCCCGCCGGTCTTTGCTCAAATAAGTGCCCTCCTCCTATGGCTTTCCTTGACC TCGACGCCCACGTCCCGCCGGTCTTTGCTCAAGTAAGTGCCCTCCTCCTATGGCTTTCCTTGACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135908707..135908897 26863196 MeRIP-seq:(Medium) rs763362785 Functional Loss SNV dbSNP153 33..33 33 - - - 94299 RMVar_ID_94299 Human_SNP_ID_417979032 m1A Human chr9 + 135911034 135911034 135911034 AGAGAGAGCCTTTAGAGCTGTGAGACAGGAGGAGGCGCCAAGGAGCCATTGCTCAGGTGGAGGGG AGAGAGAGCCTTTAGAGCTGTGAGACAGGAGGCGGCGCCAAGGAGCCATTGCTCAGGTGGAGGGG A C AL355574.1 Ensembl:ENSG00000238058 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135910989..135911136 26863196 MeRIP-seq:(Medium) rs971913932 Functional Loss SNV dbSNP153 33..33 33 - - - 94300 RMVar_ID_94300 Human_SNP_ID_417983033 m1A Human chr9 + 135924793 135924793 135924793 TCATTCCCGATGCGTCGCAGCCACATCCATCTAGTTCCAGAACACTGTCATGCCCTGGGAAGGAA TCATTCCCGATGCGTCGCAGCCACATCCATCTGGTTCCAGAACACTGTCATGCCCTGGGAAGGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:135924752..135924850 26863196 MeRIP-seq:(Medium) rs1405333896 Functional Loss SNV dbSNP153 33..33 33 - - - 94301 RMVar_ID_94301 Human_SNP_ID_417987662 m1A Human chr9 + 135939483 135939481 135939483 CTCACCACAGCCCACACTCACAGCCCACACTCACTCACCACAGCCCACACTCACTCAGCCCACAC CTCACCACAGCCCACACTCACAGCCCACACT__CTCACCACAGCCCACACTCACTCAGCCCACAC TCA T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:135939436..135939612 26863196 MeRIP-seq:(Medium) rs141027492 Functional Loss DEL dbSNP153 32..33 33 - - - 94302 RMVar_ID_94302 Human_SNP_ID_417987664 m1A Human chr9 + 135939483 135939483 135939483 CTCACCACAGCCCACACTCACAGCCCACACTCACTCACCACAGCCCACACTCACTCAGCCCACAC CTCACCACAGCCCACACTCACAGCCCACACTCCCTCACCACAGCCCACACTCACTCAGCCCACAC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:135939436..135939612 26863196 MeRIP-seq:(Medium) rs1564194978 Functional Loss SNV dbSNP153 33..33 33 - - - 94303 RMVar_ID_94303 Human_SNP_ID_417987666 m1A Human chr9 - 135939485 135939485 135939485 GAGTGTGGGCTGAGTGAGTGTGGGCTGTGGTGAGTGAGTGTGGGCTGTGAGTGTGGGCTGTGGTG GAGTGTGGGCTGAGTGAGTGTGGGCTGTGGTGGGTGAGTGTGGGCTGTGAGTGTGGGCTGTGGTG T C UBAC1 Ensembl:ENSG00000130560 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135939373..135939673 26863196 MeRIP-seq:(Medium) rs1564194981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3910638,Human_RBP_ID_5244215,Human_RBP_ID_5407548,Human_RBP_ID_5658760,Human_RBP_ID_9442478,Human_RBP_ID_17323403,Human_RBP_ID_24292327,Human_RBP_ID_26565603,Human_RBP_ID_27843935 RMVar_hsa_circ_113186,RMVar_hsa_circ_114121,RMVar_hsa_circ_103924,RMVar_hsa_circ_108556,RMVar_hsa_circ_102109,RMVar_hsa_circ_260813,RMVar_hsa_circ_260817,RMVar_hsa_circ_80175,RMVar_hsa_circ_82369,RMVar_hsa_circ_260818,RMVar_hsa_circ_260815,RMVar_hsa_circ_260816,RMVar_hsa_circ_260814,RMVar_hsa_circ_260822,RMVar_hsa_circ_260812,RMVar_hsa_circ_336038,RMVar_hsa_circ_320563 94304 RMVar_ID_94304 Human_SNP_ID_417989690 m1A Human chr9 - 135946300 135946300 135946300 GAGGTGGCGCAGAAGCTGTTAGCGCTGAACCCAGATGCAGTGGAATTGTTTAAGAAGGCGAATGG GAGGTGGCGCAGAAGCTGTTAGCGCTGAACCCGGATGCAGTGGAATTGTTTAAGAAGGCGAATGG T C UBAC1 Ensembl:ENSG00000130560 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:135945979..135946350 32194978 MeRIP-seq:(Medium) rs759877665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633911,Human_RBP_ID_24292341 Human_Splice_Rec_1098844,Human_Splice_Rec_1098845,Human_Splice_Rec_1098870,Human_Splice_Rec_1098871 Human_miRNA_ID_2234810,Human_miRNA_ID_2968603,Human_miRNA_ID_3028971 RMVar_hsa_circ_117627,RMVar_hsa_circ_113186,RMVar_hsa_circ_102109,RMVar_hsa_circ_260813,RMVar_hsa_circ_80175,RMVar_hsa_circ_82369,RMVar_hsa_circ_260815,RMVar_hsa_circ_260814,RMVar_hsa_circ_260824,RMVar_hsa_circ_260812,RMVar_hsa_circ_336038,RMVar_hsa_circ_260827,RMVar_hsa_circ_321899,RMVar_hsa_circ_354070,RMVar_hsa_circ_308236,RMVar_hsa_circ_260826,RMVar_hsa_circ_119912,RMVar_hsa_circ_260828,RMVar_hsa_circ_260829 94305 RMVar_ID_94305 Human_SNP_ID_417989691 m1A Human chr9 - 135946300 135946300 135946300 GAGGTGGCGCAGAAGCTGTTAGCGCTGAACCCAGATGCAGTGGAATTGTTTAAGAAGGCGAATGG GAGGTGGCGCAGAAGCTGTTAGCGCTGAACCCCGATGCAGTGGAATTGTTTAAGAAGGCGAATGG T G UBAC1 Ensembl:ENSG00000130560 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:135945979..135946350 32194978 MeRIP-seq:(Medium) rs759877665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633911,Human_RBP_ID_24292341 Human_Splice_Rec_1098844,Human_Splice_Rec_1098845,Human_Splice_Rec_1098870,Human_Splice_Rec_1098871 Human_miRNA_ID_2234810,Human_miRNA_ID_2968603,Human_miRNA_ID_3028971 RMVar_hsa_circ_117627,RMVar_hsa_circ_113186,RMVar_hsa_circ_102109,RMVar_hsa_circ_260813,RMVar_hsa_circ_80175,RMVar_hsa_circ_82369,RMVar_hsa_circ_260815,RMVar_hsa_circ_260814,RMVar_hsa_circ_260824,RMVar_hsa_circ_260812,RMVar_hsa_circ_336038,RMVar_hsa_circ_260827,RMVar_hsa_circ_321899,RMVar_hsa_circ_354070,RMVar_hsa_circ_308236,RMVar_hsa_circ_260826,RMVar_hsa_circ_119912,RMVar_hsa_circ_260828,RMVar_hsa_circ_260829 94306 RMVar_ID_94306 Human_SNP_ID_417990115 m1A Human chr9 + 135947727 135947727 135947727 CCAGAGAATCTCCTCTTGCTGCCCCGCCCCGCAGGAACCCCCCCACAGCAATCCCCCACACGGGG CCAGAGAATCTCCTCTTGCTGCCCCGCCCCGCGGGAACCCCCCCACAGCAATCCCCCACACGGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135947722..135947817 26863196 MeRIP-seq:(Medium) rs962260190 Functional Loss SNV dbSNP153 33..33 33 - - - 94307 RMVar_ID_94307 Human_SNP_ID_417992234 m1A Human chr9 - 135955417 135955417 135955417 TATTTTCTACCTTGAAATTTCTATTTTTCCCCAGTGTGCTCATGGGAGCTTAGAAGATCCCAAAA TATTTTCTACCTTGAAATTTCTATTTTTCCCCGGTGTGCTCATGGGAGCTTAGAAGATCCCAAAA T C UBAC1 Ensembl:ENSG00000130560 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr9:135955391..135955463;chr9:135955388..135955479;chr9:135955351..135955425 26863196,32194978 MeRIP-seq:(Medium) rs1251673918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22690548 RMVar_hsa_circ_82369,RMVar_hsa_circ_260812 94308 RMVar_ID_94308 Human_SNP_ID_417993838 m1A Human chr9 + 135961140 135961140 135961140 AGATGTGCAGCCGCAGCACCTTGCCCGCGAAGATCTTCTCCTCCTGCACGAACATCCCGCCGCCG AGATGTGCAGCCGCAGCACCTTGCCCGCGAAGGTCTTCTCCTCCTGCACGAACATCCCGCCGCCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:135961090..135961319 26863196 MeRIP-seq:(Medium) rs1170624335 Functional Loss SNV dbSNP153 33..33 33 - - - 94309 RMVar_ID_94309 Human_SNP_ID_417993890 m1A Human chr9 + 135961232 135961232 135961232 GCCCCTGAAGGTCACCGGGAAGGCGGGCGGGGAGGGGGCGGGGCCAGACCGCCCGCGCGCTCCTT GCCCCTGAAGGTCACCGGGAAGGCGGGCGGGGGGGGGGCGGGGCCAGACCGCCCGCGCGCTCCTT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:135961131..135961281 26863410 MeRIP-seq:(Medium) rs912565155 Functional Loss SNV dbSNP153 33..33 33 - - - 94310 RMVar_ID_94310 Human_SNP_ID_417993938 m1A Human chr9 - 135961325 135961325 135961325 CTGCTGCGGCGGCGGGAGCGAGGCGACCGCTGAGGCCGCGGAGAGTGACGGCGGCCCGGCCGACG CTGCTGCGGCGGCGGGAGCGAGGCGACCGCTGGGGCCGCGGAGAGTGACGGCGGCCCGGCCGACG T C UBAC1 Ensembl:ENSG00000130560 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:135961230..135961330 26863410 MeRIP-seq:(Medium) rs948354708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035997 RMVar_hsa_circ_82369,RMVar_hsa_circ_260812 94311 RMVar_ID_94311 Human_SNP_ID_418008294 m1A Human chr9 - 136010299 136010299 136010299 GCTGGGCTCCCCGTCTGCCTTGAGGGGTGTGCATGGATGGAGGGTGCCTGAGGCTGCAGGCAGGG GCTGGGCTCCCCGTCTGCCTTGAGGGGTGTGCGTGGATGGAGGGTGCCTGAGGCTGCAGGCAGGG T C NACC2 Ensembl:ENSG00000148411 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136010268..136010397 26863196 MeRIP-seq:(Medium) rs1326540439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8944718,Human_RBP_ID_9355112 Human_miRNA_ID_2896597 RMVar_hsa_circ_127352,RMVar_hsa_circ_260832 94312 RMVar_ID_94312 Human_SNP_ID_418008329 m1A Human chr9 - 136010393 136010393 136010393 CTGAGCTCAGGGCCGGACCTGGGGAGCGGGGGACTCCGCTCGGGCAGGAGGCAGCGGCCAGGGCT CTGAGCTCAGGGCCGGACCTGGGGAGCGGGGGCCTCCGCTCGGGCAGGAGGCAGCGGCCAGGGCT T G NACC2 Ensembl:ENSG00000148411 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136010189..136010555 26863196 MeRIP-seq:(Medium) rs963656046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3908204,Human_RBP_ID_8224198,Human_RBP_ID_9355112,Human_RBP_ID_18468097,Human_RBP_ID_27544033 RMVar_hsa_circ_127352,RMVar_hsa_circ_260832 94313 RMVar_ID_94313 Human_SNP_ID_418008830 m1A Human chr9 - 136011775 136011775 136011775 CGAGCAACGCATCTACGCCGAGCGGCGGGGCGACGCCGCCACCATCGTGGCTCTGAGAACTGACG CGAGCAACGCATCTACGCCGAGCGGCGGGGCGCCGCCGCCACCATCGTGGCTCTGAGAACTGACG T G NACC2 Ensembl:ENSG00000148411 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136011732..136011915 26863196 MeRIP-seq:(Medium) rs749227087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127352,RMVar_hsa_circ_260832 94314 RMVar_ID_94314 Human_SNP_ID_418017940 m1A Human chr9 + 136042676 136042676 136042676 AGACACACACACACAGAAACACACACAGACACACAGACATACACACACAGACACACACACAGACA AGACACACACACACAGAAACACACACAGACACGCAGACATACACACACAGACACACACACAGACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136042674..136042831 26863196 MeRIP-seq:(Medium) rs912672695 Functional Loss SNV dbSNP153 33..33 33 - - - 94315 RMVar_ID_94315 Human_SNP_ID_418020258 m1A Human chr9 + 136050028 136050028 136050028 CATGCTTTACTCGGGTCAGCAGCGGGATGGGCACCGAGGGGGACACGACGTAGGGGGCCGCGGCG CATGCTTTACTCGGGTCAGCAGCGGGATGGGCGCCGAGGGGGACACGACGTAGGGGGCCGCGGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136049977..136050148 26863196 MeRIP-seq:(Medium) rs1229651352 Functional Loss SNV dbSNP153 33..33 33 - - - 94316 RMVar_ID_94316 Human_SNP_ID_418027403 m1A Human chr9 - 136074769 136074769 136074769 AGGTGAGCTGGGAACAGAATGTGACCACCGACATGGGCCCTCTGGGAGTCACAGGGGATGGTCGT AGGTGAGCTGGGAACAGAATGTGACCACCGACGTGGGCCCTCTGGGAGTCACAGGGGATGGTCGT T C NACC2 Ensembl:ENSG00000148411 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136074607..136074901 26863196 MeRIP-seq:(Medium) rs959707985 Functional Loss SNV dbSNP153 33..33 33 - - - 94317 RMVar_ID_94317 Human_SNP_ID_418029675 m1A Human chr9 + 136082086 136082086 136082086 CACAAAATGGGGGCACCAGCCATTCTCCAAAGACTCTCCACCTGAACACGACCTGCCGGGGCCCT CACAAAATGGGGGCACCAGCCATTCTCCAAAGCCTCTCCACCTGAACACGACCTGCCGGGGCCCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136082038..136082232 26863196 MeRIP-seq:(Medium) rs140067700 Functional Loss SNV dbSNP153 33..33 33 - - - 94318 RMVar_ID_94318 Human_SNP_ID_418038578 m1A Human chr9 + 136109216 136109216 136109216 CAAGCCCCTTTACGAAGCCCCTTCCCAAATAGAGCCGGCGCCCTCCTCCCCTGGGCCCGGGTCAC CAAGCCCCTTTACGAAGCCCCTTCCCAAATAGTGCCGGCGCCCTCCTCCCCTGGGCCCGGGTCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136109175..136109264 26863196 MeRIP-seq:(Medium) rs773687325 Functional Loss SNV dbSNP153 33..33 33 - - - 94319 RMVar_ID_94319 Human_SNP_ID_418038733 m1A Human chr9 - 136109666 136109666 136109666 GTGCAGTCCTTGTATGGCCTCCTGCAGAGGAGAGGCCCCGTGGGAGGCGGAAGGCAGAGCTGGGT GTGCAGTCCTTGTATGGCCTCCTGCAGAGGAGGGGCCCCGTGGGAGGCGGAAGGCAGAGCTGGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136109616..136109756 26863196 MeRIP-seq:(Medium) rs1420296883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714858 94320 RMVar_ID_94320 Human_SNP_ID_418040697 m1A Human chr9 - 136115541 136115541 136115541 TTCAGTGAGCCAGGATGGAAACGCGTGTCCCAAGTGTCCGGAGCAGGCGGCAGAGGCCTCAGTGC TTCAGTGAGCCAGGATGGAAACGCGTGTCCCACGTGTCCGGAGCAGGCGGCAGAGGCCTCAGTGC T G TMEM250 Ensembl:ENSG00000238227 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136115491..136115577 26863196 MeRIP-seq:(Medium) rs1260173134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256440,Human_RBP_ID_5019009 Human_Splice_Rec_1098913 Human_miRNA_ID_2478974 RMVar_hsa_circ_76151,RMVar_hsa_circ_260837 94321 RMVar_ID_94321 Human_SNP_ID_418040780 m1A Human chr9 + 136115775 136115775 136115775 GGAGTCAGCCCCTGGCTCCCAGGGTTCCCCCCAGGCCAGCCCCTGAGCTGGGAGCCTGCTGAGGC GGAGTCAGCCCCTGGCTCCCAGGGTTCCCCCCGGGCCAGCCCCTGAGCTGGGAGCCTGCTGAGGC A G NONHSAG053785.2 RNACentral:URS00008C2D03 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136115728..136115879 32194978 MeRIP-seq:(Medium) rs1392586888 Functional Loss SNV dbSNP153 33..33 33 - - - 94322 RMVar_ID_94322 Human_SNP_ID_418040985 m1A Human chr9 + 136116452 136116452 136116452 CACCCATGGAGAGAACACAGCCACAGGCCGGGACGATACATCAAGCTCGCACCCACGGCCCTCAC CACCCATGGAGAGAACACAGCCACAGGCCGGGGCGATACATCAAGCTCGCACCCACGGCCCTCAC A G NONHSAG053785.2 RNACentral:URS00008C2D03 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136116228..136116678 32194978 MeRIP-seq:(Medium) rs746393891 Functional Loss SNV dbSNP153 33..33 33 - - - 94323 RMVar_ID_94323 Human_SNP_ID_418041199 m1A Human chr9 + 136116828 136116828 136116828 GCGGGCCAGGTGGGAGGCGCGCACGGGCCCGCAGGCCGCATGCAGGCAGGTGGTGTGCGGGCCGT GCGGGCCAGGTGGGAGGCGCGCACGGGCCCGCTGGCCGCATGCAGGCAGGTGGTGTGCGGGCCGT A T NONHSAG053785.2 RNACentral:URS00008C2D03 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136116777..136116878 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 94324 RMVar_ID_94324 Human_SNP_ID_418041252 m1A Human chr9 - 136116901 136116901 136116901 ACTGCGACCTAGCGCCGCCGCCGCCGGGGCCCAATGCCGGTCATGCCCATTCCGCGGCGGGTGCG ACTGCGACCTAGCGCCGCCGCCGCCGGGGCCCTATGCCGGTCATGCCCATTCCGCGGCGGGTGCG T A TMEM250 Ensembl:ENSG00000238227 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136116801..136117918;chr9:136116851..136117025;chr9:136116860..136117046 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1409938986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036001,Human_RBP_ID_27544093 Human_miRNA_ID_2295450 RMVar_hsa_circ_76151,RMVar_hsa_circ_260837 94325 RMVar_ID_94325 Human_SNP_ID_418041301 m1A Human chr9 - 136116959 136116959 136116959 CCCAGGCCTAGGCGCCCATGACCCCTACGCCAACAGCCGCCTGGACACCGCCGCCGCCACTGCGA CCCAGGCCTAGGCGCCCATGACCCCTACGCCAGCAGCCGCCTGGACACCGCCGCCGCCACTGCGA T C TMEM250 Ensembl:ENSG00000238227 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr9:136116877..136116977 26863410 MeRIP-seq:(Medium) rs1353056163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256442,Human_RBP_ID_798163,Human_RBP_ID_26562387,Human_RBP_ID_27544094 Human_Splice_Rec_1098910,Human_Splice_Rec_1098912,Human_Splice_Rec_1098916,Human_Splice_Rec_1098918,Human_Splice_Rec_1098920 RMVar_hsa_circ_76151,RMVar_hsa_circ_260837 94326 RMVar_ID_94326 Human_SNP_ID_418041957 m1A Human chr9 + 136118688 136118688 136118688 ACGCGTCGCCGGCTGGGGTCGCCCTGCAGGTGAAGGGGCTCTCGGGCGCGGCCGCCGGAGGCGTT ACGCGTCGCCGGCTGGGGTCGCCCTGCAGGTGTAGGGGCTCTCGGGCGCGGCCGCCGGAGGCGTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136118439..136118857 26863196 MeRIP-seq:(Medium) rs965101676 Functional Loss SNV dbSNP153 33..33 33 - - - 94327 RMVar_ID_94327 Human_SNP_ID_418041983 m1A Human chr9 - 136118775 136118775 136118775 GCGGCTCGGTCGGCGCGGGTGGAGGGGGCGTGAGGCCGCCCTACGGTGGCCGTCGAGGGACGGCG GCGGCTCGGTCGGCGCGGGTGGAGGGGGCGTGGGGCCGCCCTACGGTGGCCGTCGAGGGACGGCG T C TMEM250 Ensembl:ENSG00000238227 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136118444..136118875;chr9:136118435..136118850 26863196 MeRIP-seq:(Medium) rs888019313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256943,Human_RBP_ID_5036003,Human_RBP_ID_8944658,Human_RBP_ID_18453311,Human_RBP_ID_22748312 94328 RMVar_ID_94328 Human_SNP_ID_418042241 m1A Human chr9 - 136119244 136119243 136119245 CATTCCCGCCGCCGCCCTGTCCTCCCAGCCCCAGGCCGCGCAGGAGGCCTTCGCACACGGCCCCG CATTCCCGCCGCCGCCCTGTCCTCCCAGCCC__GGCCGCGCAGGAGGCCTTCGCACACGGCCCCG CTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136119194..136119392 26863196 MeRIP-seq:(Medium) rs748863650 Functional Loss DEL dbSNP153 32..33 33 - - - 94329 RMVar_ID_94329 Human_SNP_ID_418042255 m1A Human chr9 + 136119274 136119274 136119274 CCTGGGGCTGGGAGGACAGGGCGGCGGCGGGAATGAGGGCGCCCCCCAGGCTCCAGGAGGGCGGG CCTGGGGCTGGGAGGACAGGGCGGCGGCGGGAGTGAGGGCGCCCCCCAGGCTCCAGGAGGGCGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136119135..136119431 26863196 MeRIP-seq:(Medium) rs747032742 Functional Loss SNV dbSNP153 33..33 33 - - - 94330 RMVar_ID_94330 Human_SNP_ID_418078131 m1A Human chr9 - 136236962 136236962 136236962 GACGCCGGCCCAGGACAGGCTCCAGGTGTGGCACAGGACGGGCACCAGGTGATGCAGGCCCAGGA GACGCCGGCCCAGGACAGGCTCCAGGTGTGGCGCAGGACGGGCACCAGGTGATGCAGGCCCAGGA T C QSOX2 Ensembl:ENSG00000165661 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136236960..136237082 26863196 MeRIP-seq:(Medium) rs1169189538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84379,RMVar_hsa_circ_92215,RMVar_hsa_circ_260842,RMVar_hsa_circ_260845,RMVar_hsa_circ_260847,RMVar_hsa_circ_107211 94331 RMVar_ID_94331 Human_SNP_ID_418080430 m1A Human chr9 - 136245550 136245550 136245550 CACCGCCAACAGCTCGGCCGCGTGGCTCGTGCAGTTCTACTCGTCGTGGTGTGGCCACTGCATCG CACCGCCAACAGCTCGGCCGCGTGGCTCGTGCGGTTCTACTCGTCGTGGTGTGGCCACTGCATCG T C QSOX2 Ensembl:ENSG00000165661 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136245501..136245600 32194978 MeRIP-seq:(Medium) rs1554758413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1098959 RMVar_hsa_circ_84379,RMVar_hsa_circ_92215,RMVar_hsa_circ_260842,RMVar_hsa_circ_260845,RMVar_hsa_circ_260847,RMVar_hsa_circ_107211 94332 RMVar_ID_94332 Human_SNP_ID_418098506 m1A Human chr9 + 136308585 136308585 136308585 AATACACAGACAATACACATCACACATAACACACAGACAACACACACACCACACACAAACGCACA AATACACAGACAATACACATCACACATAACACTCAGACAACACACACACCACACACAAACGCACA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136308579..136308706 26863196 MeRIP-seq:(Medium) rs1370711688 Functional Loss SNV dbSNP153 33..33 33 - - - 94333 RMVar_ID_94333 Human_SNP_ID_418104227 m1A Human chr9 + 136329328 136329328 136329328 CCCCGGGAGTCTGCACCCCACCGTGTAGCCACAGCCCGGTTTGGGCAGGCGGTTCCTGGTCGGAG CCCCGGGAGTCTGCACCCCACCGTGTAGCCACGGCCCGGTTTGGGCAGGCGGTTCCTGGTCGGAG A G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136329325..136329443 32194978 MeRIP-seq:(Medium) rs959578499 Functional Loss SNV dbSNP153 33..33 33 - - - 94334 RMVar_ID_94334 Human_SNP_ID_418105854 m1A Human chr9 + 136334679 136334678 136334679 AGCATGACCTCCTGCTGGCGCGGTGAGTGGGGACGGTCCTGCTGGCGGGTGAGTGGGGCGGCCCT AGCATGACCTCCTGCTGGCGCGGTGAGTGGGG_CGGTCCTGCTGGCGGGTGAGTGGGGCGGCCCT GA G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136334676..136334839 26863196 MeRIP-seq:(Medium) rs782168146 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_260848,RMVar_hsa_circ_317492 94335 RMVar_ID_94335 Human_SNP_ID_418105855 m1A Human chr9 + 136334679 136334679 136334679 AGCATGACCTCCTGCTGGCGCGGTGAGTGGGGACGGTCCTGCTGGCGGGTGAGTGGGGCGGCCCT AGCATGACCTCCTGCTGGCGCGGTGAGTGGGGCCGGTCCTGCTGGCGGGTGAGTGGGGCGGCCCT A C GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136334676..136334839 26863196 MeRIP-seq:(Medium) rs782322719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260848,RMVar_hsa_circ_317492 94336 RMVar_ID_94336 Human_SNP_ID_418107278 m1A Human chr9 + 136338626 136338626 136338626 AGTGGAGGCGCAGGCCTGCTACAGTCTGGGCAACACCTACACGCTGCTGCAGGACTACGAGCGCG AGTGGAGGCGCAGGCCTGCTACAGTCTGGGCATCACCTACACGCTGCTGCAGGACTACGAGCGCG A T GPSM1 Ensembl:ENSG00000160360 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136338575..136341025 32194978 MeRIP-seq:(Medium) rs782398108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099114,Human_Splice_Rec_1099115,Human_Splice_Rec_1099130,Human_Splice_Rec_1099131,Human_Splice_Rec_1099156,Human_Splice_Rec_1099157 Human_miRNA_ID_2756521,Human_miRNA_ID_2756522 RMVar_hsa_circ_260848,RMVar_hsa_circ_317492 94337 RMVar_ID_94337 Human_SNP_ID_418109191 m1A Human chr9 - 136344756 136344752 136344756 CAGCTCCAGACAGTCTCCCTGTCCCTTCACCTACCAGGCTGGCCCCTGCCTCAGGCCCTTTGCAC CAGCTCCAGACAGTCTCCCTGTCCCTTCACCT___AGGCTGGCCCCTGCCTCAGGCCCTTTGCAC CTGGT CT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136344752..136344873 26863196 MeRIP-seq:(Medium) rs386739576 Functional Loss DEL dbSNP153 33..35 33 - - - 94338 RMVar_ID_94338 Human_SNP_ID_418109193 m1A Human chr9 - 136344756 136344756 136344756 CAGCTCCAGACAGTCTCCCTGTCCCTTCACCTACCAGGCTGGCCCCTGCCTCAGGCCCTTTGCAC CAGCTCCAGACAGTCTCCCTGTCCCTTCACCTGCCAGGCTGGCCCCTGCCTCAGGCCCTTTGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136344752..136344873 26863196 MeRIP-seq:(Medium) rs1325300367 Functional Loss SNV dbSNP153 33..33 33 - - - 94339 RMVar_ID_94339 Human_SNP_ID_418109254 m1A Human chr9 + 136344986 136344986 136344986 GGCAAGGCTGGGGCAGCAGGCAGGTGAGGGGCAGGTGATCCGGCTCCAGGGAGGTGAGGAGGGGT GGCAAGGCTGGGGCAGCAGGCAGGTGAGGGGCGGGTGATCCGGCTCCAGGGAGGTGAGGAGGGGT A G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136344981..136345366 26863196 MeRIP-seq:(Medium) rs1427167723 Functional Loss SNV dbSNP153 33..33 33 - - - 94340 RMVar_ID_94340 Human_SNP_ID_418111772 m1A Human chr9 - 136352518 136352518 136352518 TGCCTCTCTGTCTCATTCCTGGTTGGACCTACACTGTCTCCAGCCTCTGAGGCCAACCCTGCCCT TGCCTCTCTGTCTCATTCCTGGTTGGACCTACGCTGTCTCCAGCCTCTGAGGCCAACCCTGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136352468..136352614 26863196 MeRIP-seq:(Medium) rs1402681077 Functional Loss SNV dbSNP153 33..33 33 - - - 94341 RMVar_ID_94341 Human_SNP_ID_418111976 m1A Human chr9 + 136353205 136353205 136353205 GGGGTCCTAACAGGTGGAGGCTGAGGGAGCACACGGGCCTCTGTGAAGCCGGGTGGGGTGGTCTT GGGGTCCTAACAGGTGGAGGCTGAGGGAGCACTCGGGCCTCTGTGAAGCCGGGTGGGGTGGTCTT A T GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:136353154..136353352;chr9:136353159..136353358 26863196 MeRIP-seq:(Medium) rs1554772432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906584,Human_RBP_ID_5244016,Human_RBP_ID_8160521 94342 RMVar_ID_94342 Human_SNP_ID_418112148 m1A Human chr9 + 136353762 136353762 136353762 TCACCTGGGGGAGTCCAGATTGGGCCAGAGGCAGAGGCCCCCCGCGGCTGTGCCCTAGGTCATCA TCACCTGGGGGAGTCCAGATTGGGCCAGAGGCGGAGGCCCCCCGCGGCTGTGCCCTAGGTCATCA A G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136353761..136353866 32194978 MeRIP-seq:(Medium) rs1049833387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3910101,Human_RBP_ID_26795993 94343 RMVar_ID_94343 Human_SNP_ID_418112611 m1A Human chr9 + 136355069 136355068 136355069 CTGGGGGAGGGGTAGCCGGGTGCCGAGGGTGGATGACACATCCTGGGAGAGGGGTAGCCGGGTGC CTGGGGGAGGGGTAGCCGGGTGCCGAGGGTGG_TGACACATCCTGGGAGAGGGGTAGCCGGGTGC GA G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:136354976..136355158 26863196 MeRIP-seq:(Medium) rs59335446 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5227433,Human_RBP_ID_8224308,Human_RBP_ID_8238994,Human_RBP_ID_9442503,Human_RBP_ID_18962555 GWAS_ID_12245,GWAS_ID_12246,GWAS_ID_12247,GWAS_ID_12248,GWAS_ID_12249,GWAS_ID_12250,GWAS_ID_12251,GWAS_ID_12252,GWAS_ID_12253,GWAS_ID_12254,GWAS_ID_12255,GWAS_ID_12256,GWAS_ID_12257,GWAS_ID_12258,GWAS_ID_12259,GWAS_ID_12260,GWAS_ID_12261,GWAS_ID_12262,GWAS_ID_12263,GWAS_ID_12264,GWAS_ID_12265,GWAS_ID_12266,GWAS_ID_12267,GWAS_ID_12268,GWAS_ID_12269,GWAS_ID_12270,GWAS_ID_12271,GWAS_ID_12272,GWAS_ID_12273,GWAS_ID_12274,GWAS_ID_12275,GWAS_ID_12276,GWAS_ID_12277,GWAS_ID_12278,GWAS_ID_12279,GWAS_ID_12280,GWAS_ID_12281,GWAS_ID_12282,GWAS_ID_12283,GWAS_ID_12284,GWAS_ID_12285,GWAS_ID_12286,GWAS_ID_12287,GWAS_ID_12288,GWAS_ID_12289,GWAS_ID_12290,GWAS_ID_12291,GWAS_ID_12292,GWAS_ID_12293,GWAS_ID_12294,GWAS_ID_12295 94344 RMVar_ID_94344 Human_SNP_ID_418112615 m1A Human chr9 + 136355069 136355069 136355069 CTGGGGGAGGGGTAGCCGGGTGCCGAGGGTGGATGACACATCCTGGGAGAGGGGTAGCCGGGTGC CTGGGGGAGGGGTAGCCGGGTGCCGAGGGTGGGTGACACATCCTGGGAGAGGGGTAGCCGGGTGC A G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:136354976..136355158 26863196 MeRIP-seq:(Medium) rs62579164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227433,Human_RBP_ID_8224308,Human_RBP_ID_8238994,Human_RBP_ID_9442503,Human_RBP_ID_18962555 94345 RMVar_ID_94345 Human_SNP_ID_418112694 m1A Human chr9 + 136355560 136355534 136355561 GGGTGACACGTTCTGGGGGAGGGGTAGCCGACAGGGGGCAGGTTAGAGTCCCGATCTTGGCCAGG GGGTGAC___________________________GGGGCAGGTTAGAGTCCCGATCTTGGCCAGG CACGTTCTGGGGGAGGGGTAGCCGACAG C GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136355513..136355852 26863196 MeRIP-seq:(Medium) rs1554772821 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_268738,Human_RBP_ID_965123,Human_RBP_ID_3906592,Human_RBP_ID_3975119,Human_RBP_ID_5229453,Human_RBP_ID_5329749,Human_RBP_ID_8159738,Human_RBP_ID_8224309,Human_RBP_ID_8239092,Human_RBP_ID_8944726,Human_RBP_ID_9442151,Human_RBP_ID_17202286,Human_RBP_ID_24443588 94346 RMVar_ID_94346 Human_SNP_ID_418112702 m1A Human chr9 + 136355560 136355559 136355561 GGGTGACACGTTCTGGGGGAGGGGTAGCCGACAGGGGGCAGGTTAGAGTCCCGATCTTGGCCAGG GGGTGACACGTTCTGGGGGAGGGGTAGCCGAC__GGGGCAGGTTAGAGTCCCGATCTTGGCCAGG CAG C GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136355513..136355852 26863196 MeRIP-seq:(Medium) rs10647805 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_268738,Human_RBP_ID_965123,Human_RBP_ID_3906592,Human_RBP_ID_3975119,Human_RBP_ID_5229453,Human_RBP_ID_5329749,Human_RBP_ID_8159738,Human_RBP_ID_8224309,Human_RBP_ID_8239092,Human_RBP_ID_8944726,Human_RBP_ID_9442151,Human_RBP_ID_17202286,Human_RBP_ID_24443588 94347 RMVar_ID_94347 Human_SNP_ID_418112704 m1A Human chr9 + 136355560 136355560 136355560 GGGTGACACGTTCTGGGGGAGGGGTAGCCGACAGGGGGCAGGTTAGAGTCCCGATCTTGGCCAGG GGGTGACACGTTCTGGGGGAGGGGTAGCCGACGGGGGGCAGGTTAGAGTCCCGATCTTGGCCAGG A G GPSM1 Ensembl:ENSG00000160360 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136355513..136355852 26863196 MeRIP-seq:(Medium) rs1328135601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268738,Human_RBP_ID_965123,Human_RBP_ID_3906592,Human_RBP_ID_3975119,Human_RBP_ID_5229453,Human_RBP_ID_5329749,Human_RBP_ID_8159738,Human_RBP_ID_8224309,Human_RBP_ID_8239092,Human_RBP_ID_8944726,Human_RBP_ID_9442151,Human_RBP_ID_17202286,Human_RBP_ID_24443588 94348 RMVar_ID_94348 Human_SNP_ID_418113843 m1A Human chr9 - 136358126 136358126 136358126 GGCCCCCGGCGAGGTCCACCCGCTGCTCGTCCATGCGCTTAGCCTGCACCCTCTGAATGAGGCTG GGCCCCCGGCGAGGTCCACCCGCTGCTCGTCCGTGCGCTTAGCCTGCACCCTCTGAATGAGGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136358077..136358269 26863196 MeRIP-seq:(Medium) rs782545530 Functional Loss SNV dbSNP153 33..33 33 - - - 94349 RMVar_ID_94349 Human_SNP_ID_418113857 m1A Human chr9 - 136358147 136358147 136358147 GGCCGCCTGCCCCCTGCTCCGGGCCCCCGGCGAGGTCCACCCGCTGCTCGTCCATGCGCTTAGCC GGCCGCCTGCCCCCTGCTCCGGGCCCCCGGCGGGGTCCACCCGCTGCTCGTCCATGCGCTTAGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136358096..136358324 26863196 MeRIP-seq:(Medium) rs1554773586 Functional Loss SNV dbSNP153 33..33 33 - - - 94350 RMVar_ID_94350 Human_SNP_ID_418114074 m1A Human chr9 - 136358638 136358637 136358638 CACACGGCCATCCCAAGACCAGCTCTGGGGGGACAGAACATGGCCCTGTCCTTGGTGGCCCCAAG CACACGGCCATCCCAAGACCAGCTCTGGGGGG_CAGAACATGGCCCTGTCCTTGGTGGCCCCAAG GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136358373..136358775 26863196 MeRIP-seq:(Medium) rs1182961863 Functional Loss DEL dbSNP153 33..33 33 - - - 94351 RMVar_ID_94351 Human_SNP_ID_418116024 m1A Human chr9 - 136363567 136363567 136363567 GGCGGGCCTGGGCCTGGGGCTGGCGGCGCTCAAGCTCCGAGCAGGGGCCGGGGCCCGCGGCGGCT GGCGGGCCTGGGCCTGGGGCTGGCGGCGCTCACGCTCCGAGCAGGGGCCGGGGCCCGCGGCGGCT T G DNLZ,CARD9 Ensembl:ENSG00000213221,Ensembl:ENSG00000187796 Protein coding,Protein coding CDS,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136363562..136363725 26863196 MeRIP-seq:(Medium) rs778158039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099187,Human_Splice_Rec_1099189 94352 RMVar_ID_94352 Human_SNP_ID_418116122 m1A Human chr9 + 136363710 136363710 136363710 GCAACCTCGGCGCGCCGCGCAGCGCAGTCCGCAGCATCCCGCTCGCCGGCTCCGTCCGCCCTGCC GCAACCTCGGCGCGCCGCGCAGCGCAGTCCGCGGCATCCCGCTCGCCGGCTCCGTCCGCCCTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:136361950..136363775;chr9:136361952..136363789;chr9:136362052..136363911 26863196 MeRIP-seq:(Medium) rs1378882204 Functional Loss SNV dbSNP153 33..33 33 - - - 94353 RMVar_ID_94353 Human_SNP_ID_418116123 m1A Human chr9 + 136363710 136363710 136363710 GCAACCTCGGCGCGCCGCGCAGCGCAGTCCGCAGCATCCCGCTCGCCGGCTCCGTCCGCCCTGCC GCAACCTCGGCGCGCCGCGCAGCGCAGTCCGCTGCATCCCGCTCGCCGGCTCCGTCCGCCCTGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:136361950..136363775;chr9:136361952..136363789;chr9:136362052..136363911 26863196 MeRIP-seq:(Medium) rs1378882204 Functional Loss SNV dbSNP153 33..33 33 - - - 94354 RMVar_ID_94354 Human_SNP_ID_418117892 m1A Human chr9 - 136367659 136367659 136367659 GCTACTGGCCGTGGAGGGCAGGCTCAGGCGGCAGCAGCTGGAGACGCTCGTCCTGGTGGGCCTGG GCTACTGGCCGTGGAGGGCAGGCTCAGGCGGCGGCAGCTGGAGACGCTCGTCCTGGTGGGCCTGG T C CARD9 Ensembl:ENSG00000187796 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136367613..136367738 26863196 MeRIP-seq:(Medium) rs1372834289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19144319,Human_RBP_ID_22838148,Human_RBP_ID_23094549 Human_Splice_Rec_1099207,Human_Splice_Rec_1099239,Human_Splice_Rec_1099263,Human_Splice_Rec_1099293 RMVar_hsa_circ_42372 94355 RMVar_ID_94355 Human_SNP_ID_418121621 m1A Human chr9 - 136377591 136377591 136377591 GATGAAGACCTCCTGAGTGAGCTGGAACTTGCAGACAGGGACGGGCAGCCGGGCTGCACGACAGC GATGAAGACCTCCTGAGTGAGCTGGAACTTGCGGACAGGGACGGGCAGCCGGGCTGCACGACAGC T C SNAPC4 Ensembl:ENSG00000165684 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136377541..136377809 26863196 MeRIP-seq:(Medium) rs771038292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1703357,Human_RBP_ID_3895505,Human_RBP_ID_5535217,Human_RBP_ID_22838151,Human_RBP_ID_27544140 Human_Splice_Rec_1099355 Human_miRNA_ID_1967219,Human_miRNA_ID_2444009 RMVar_hsa_circ_96571,RMVar_hsa_circ_99270,RMVar_hsa_circ_260855,RMVar_hsa_circ_260857,RMVar_hsa_circ_77763,RMVar_hsa_circ_260856,RMVar_hsa_circ_102139,RMVar_hsa_circ_260859 94356 RMVar_ID_94356 Human_SNP_ID_418122055 m1A Human chr9 - 136378233 136378233 136378233 AGGACGTCCTCCCACGCTGACCCTCCTGAAGCAGAACCCCCTTGGTCCGGGAGGCTGCCAGCCTT AGGACGTCCTCCCACGCTGACCCTCCTGAAGCGGAACCCCCTTGGTCCGGGAGGCTGCCAGCCTT T C SNAPC4 Ensembl:ENSG00000165684 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136378105..136378324 26863196 MeRIP-seq:(Medium) rs1196081301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23091004,Human_RBP_ID_27544144 RMVar_hsa_circ_96571,RMVar_hsa_circ_99270,RMVar_hsa_circ_260855,RMVar_hsa_circ_260857,RMVar_hsa_circ_77763,RMVar_hsa_circ_260856,RMVar_hsa_circ_102139,RMVar_hsa_circ_260859 94357 RMVar_ID_94357 Human_SNP_ID_418122543 m1A Human chr9 + 136379041 136379041 136379041 GGCCGTGTGGGGTGTGTGGTAGAGGGGGCTGGAGGATCACAGACGAGGAGACCAGCAGCTGGGAC GGCCGTGTGGGGTGTGTGGTAGAGGGGGCTGGTGGATCACAGACGAGGAGACCAGCAGCTGGGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136378990..136379090 26863196 MeRIP-seq:(Medium) rs1037019895 Functional Loss SNV dbSNP153 33..33 33 - - - 94358 RMVar_ID_94358 Human_SNP_ID_418124341 m1A Human chr9 - 136383599 136383599 136383599 GTCACAGCGTCCGGTGGAGCTCTACCAGCAGCAGCGGCAGCAGCAGTGGCAGCAGTGGAGGGAGC GTCACAGCGTCCGGTGGAGCTCTACCAGCAGCGGCGGCAGCAGCAGTGGCAGCAGTGGAGGGAGC T C SNAPC4 Ensembl:ENSG00000165684 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136383424..136383958 32194978 MeRIP-seq:(Medium) rs1242518923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797851,Human_RBP_ID_19026048 Human_Splice_Rec_1099342 RMVar_hsa_circ_99270,RMVar_hsa_circ_260857,RMVar_hsa_circ_77763,RMVar_hsa_circ_260856,RMVar_hsa_circ_60273 94359 RMVar_ID_94359 Human_SNP_ID_418126062 m1A Human chr9 + 136388522 136388522 136388522 CTGCGTGAGCATGCGGTCCTCCTCCTCTGTCCACTCCTTGCGTTTCAGAGCTTTGTTGTGCTGCT CTGCGTGAGCATGCGGTCCTCCTCCTCTGTCCGCTCCTTGCGTTTCAGAGCTTTGTTGTGCTGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136388471..136391972 32194978 MeRIP-seq:(Medium) rs762164868 Functional Loss SNV dbSNP153 33..33 33 - - - 94360 RMVar_ID_94360 Human_SNP_ID_418127592 m1A Human chr9 - 136392772 136392772 136392772 CCCTTCTGCCTCTGCTCTGCTTTGCAGGCTCGAGTACTTGCACCAGAAGCAGAGCAAAGTCTCCA CCCTTCTGCCTCTGCTCTGCTTTGCAGGCTCGCGTACTTGCACCAGAAGCAGAGCAAAGTCTCCA T G SNAPC4 Ensembl:ENSG00000165684 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs767522548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22556820,Human_RBP_ID_22690568 Human_Splice_Rec_1099326,Human_Splice_Rec_1099327,Human_Splice_Rec_1099372,Human_Splice_Rec_1099373 RMVar_hsa_circ_99270,RMVar_hsa_circ_260857,RMVar_hsa_circ_77763,RMVar_hsa_circ_260856,RMVar_hsa_circ_65536,RMVar_hsa_circ_60273,RMVar_hsa_circ_119623,RMVar_hsa_circ_82945,RMVar_hsa_circ_260860,RMVar_hsa_circ_260861,RMVar_hsa_circ_49477,RMVar_hsa_circ_330289 94361 RMVar_ID_94361 Human_SNP_ID_418128577 m1A Human chr9 + 136395373 136395373 136395373 CCCATGTATGTGCTTGGGGGCAGGCTTTTGCCATCTTTCACCTTGGTGCCTTTGGACCCAGCCAG CCCATGTATGTGCTTGGGGGCAGGCTTTTGCCGTCTTTCACCTTGGTGCCTTTGGACCCAGCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136395322..136397008 32194978 MeRIP-seq:(Medium) rs4266763 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_538 GWAS_ID_12296,GWAS_ID_12297,GWAS_ID_12298,GWAS_ID_12299,GWAS_ID_12300,GWAS_ID_12301,GWAS_ID_12302,GWAS_ID_12303,GWAS_ID_12304,GWAS_ID_12305,GWAS_ID_12306,GWAS_ID_12307,GWAS_ID_12308,GWAS_ID_12309,GWAS_ID_12310,GWAS_ID_12311,GWAS_ID_12312,GWAS_ID_12313,GWAS_ID_12314,GWAS_ID_12315,GWAS_ID_12316,GWAS_ID_12317,GWAS_ID_12318,GWAS_ID_12319,GWAS_ID_12320,GWAS_ID_12321,GWAS_ID_12322,GWAS_ID_12323,GWAS_ID_12324,GWAS_ID_12325,GWAS_ID_12326,GWAS_ID_12327,GWAS_ID_12328,GWAS_ID_12329,GWAS_ID_12330,GWAS_ID_12331,GWAS_ID_12332,GWAS_ID_12333,GWAS_ID_12334,GWAS_ID_12335,GWAS_ID_12336,GWAS_ID_12337,GWAS_ID_12338,GWAS_ID_12339,GWAS_ID_12340,GWAS_ID_12341,GWAS_ID_12342,GWAS_ID_12343,GWAS_ID_12344,GWAS_ID_12345,GWAS_ID_12346,GWAS_ID_12347,GWAS_ID_12348,GWAS_ID_12349,GWAS_ID_12350,GWAS_ID_12351,GWAS_ID_12352,GWAS_ID_12353,GWAS_ID_12354,GWAS_ID_12355,GWAS_ID_12356,GWAS_ID_12357,GWAS_ID_12358,GWAS_ID_12359,GWAS_ID_12360,GWAS_ID_12361,GWAS_ID_12362,GWAS_ID_12363,GWAS_ID_12364,GWAS_ID_12365,GWAS_ID_12366,GWAS_ID_12367,GWAS_ID_12368,GWAS_ID_12369,GWAS_ID_12370,GWAS_ID_12371,GWAS_ID_12372,GWAS_ID_12373,GWAS_ID_12374,GWAS_ID_12375,GWAS_ID_12376,GWAS_ID_12377,GWAS_ID_12378,GWAS_ID_12379,GWAS_ID_12380,GWAS_ID_12381,GWAS_ID_12382,GWAS_ID_12383,GWAS_ID_12384,GWAS_ID_12385,GWAS_ID_12386,GWAS_ID_12387,GWAS_ID_12388,GWAS_ID_12389,GWAS_ID_12390,GWAS_ID_12391,GWAS_ID_12392,GWAS_ID_12393,GWAS_ID_12394,GWAS_ID_12395,GWAS_ID_12396,GWAS_ID_12397,GWAS_ID_12398,GWAS_ID_12399,GWAS_ID_12400,GWAS_ID_12401,GWAS_ID_12402,GWAS_ID_12403,GWAS_ID_12404,GWAS_ID_12405,GWAS_ID_12406,GWAS_ID_12407,GWAS_ID_12408,GWAS_ID_12409,GWAS_ID_12410,GWAS_ID_12411,GWAS_ID_12412,GWAS_ID_12413,GWAS_ID_12414,GWAS_ID_12415,GWAS_ID_12416,GWAS_ID_12417,GWAS_ID_12418,GWAS_ID_12419,GWAS_ID_12420,GWAS_ID_12421,GWAS_ID_12422,GWAS_ID_12423,GWAS_ID_12424,GWAS_ID_12425,GWAS_ID_12426,GWAS_ID_12427,GWAS_ID_12428,GWAS_ID_12429,GWAS_ID_12430,GWAS_ID_12431,GWAS_ID_12432,GWAS_ID_12433,GWAS_ID_12434,GWAS_ID_12435,GWAS_ID_12436,GWAS_ID_12437,GWAS_ID_12438,GWAS_ID_12439,GWAS_ID_12440,GWAS_ID_12441,GWAS_ID_12442,GWAS_ID_12443,GWAS_ID_12444,GWAS_ID_12445,GWAS_ID_12446,GWAS_ID_12447,GWAS_ID_12448,GWAS_ID_12449,GWAS_ID_12450,GWAS_ID_12451,GWAS_ID_12452,GWAS_ID_12453,GWAS_ID_12454,GWAS_ID_12455,GWAS_ID_12456,GWAS_ID_12457,GWAS_ID_12458,GWAS_ID_12459,GWAS_ID_12460,GWAS_ID_12461 94362 RMVar_ID_94362 Human_SNP_ID_418131675 m1A Human chr9 - 136404118 136404118 136404118 CGGCCAGGGTGCCAGCCTGACCGTGGTGAAGCAGAACGCCGACGTGGCCCTGCAGAACCTCCGGG CGGCCAGGGTGCCAGCCTGACCGTGGTGAAGCGGAACGCCGACGTGGCCCTGCAGAACCTCCGGG T C ENTR1 Ensembl:ENSG00000165689 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136403956..136404156 26863196 MeRIP-seq:(Medium) rs368069637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715018 Human_Splice_Rec_1099400,Human_Splice_Rec_1099401,Human_Splice_Rec_1099416,Human_Splice_Rec_1099417,Human_Splice_Rec_1099430,Human_Splice_Rec_1099431,Human_Splice_Rec_1099436,Human_Splice_Rec_1099437,Human_Splice_Rec_1099448,Human_Splice_Rec_1099449,Human_Splice_Rec_1099452,Human_Splice_Rec_1099453,Human_Splice_Rec_1099462 RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018,RMVar_hsa_circ_61004 94363 RMVar_ID_94363 Human_SNP_ID_418131955 m1A Human chr9 + 136404766 136404766 136404766 TGTCCTCACATTCATACCGGACACGGGCCCCAACCCAGGGAGCAGGAGGGCACCCAACCTGGCTG TGTCCTCACATTCATACCGGACACGGGCCCCATCCCAGGGAGCAGGAGGGCACCCAACCTGGCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:136404720..136404967;chr9:136404732..136405052 26863196 MeRIP-seq:(Medium) rs1255806931 Functional Loss SNV dbSNP153 33..33 33 - - - 94364 RMVar_ID_94364 Human_SNP_ID_418131957 m1A Human chr9 + 136404774 136404774 136404774 CATTCATACCGGACACGGGCCCCAACCCAGGGAGCAGGAGGGCACCCAACCTGGCTGTGGCCCTT CATTCATACCGGACACGGGCCCCAACCCAGGGGGCAGGAGGGCACCCAACCTGGCTGTGGCCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136404739..136404943 26863196 MeRIP-seq:(Medium) rs1333379506 Functional Loss SNV dbSNP153 33..33 33 - - - 94365 RMVar_ID_94365 Human_SNP_ID_418132065 m1A Human chr9 + 136405081 136405081 136405081 CTGCCCCACCCAGCTCGTCCGATTCAGAGAAGAAACCCATACGGTCATCAGCTCCAGGTTCTGCT CTGCCCCACCCAGCTCGTCCGATTCAGAGAAGCAACCCATACGGTCATCAGCTCCAGGTTCTGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136405041..136405112 26863196 MeRIP-seq:(Medium) rs372652609 Functional Loss SNV dbSNP153 33..33 33 - - - 94366 RMVar_ID_94366 Human_SNP_ID_418132066 m1A Human chr9 + 136405081 136405081 136405081 CTGCCCCACCCAGCTCGTCCGATTCAGAGAAGAAACCCATACGGTCATCAGCTCCAGGTTCTGCT CTGCCCCACCCAGCTCGTCCGATTCAGAGAAGGAACCCATACGGTCATCAGCTCCAGGTTCTGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136405041..136405112 26863196 MeRIP-seq:(Medium) rs372652609 Functional Loss SNV dbSNP153 33..33 33 - - - 94367 RMVar_ID_94367 Human_SNP_ID_418132880 m1A Human chr9 - 136407214 136407214 136407214 TCTCCGGCCTCTCCGGCAGGGAGTCCTAGCGCAGACTTTGCGGTTCATGGAGAGTCTCTGGGAGA TCTCCGGCCTCTCCGGCAGGGAGTCCTAGCGCTGACTTTGCGGTTCATGGAGAGTCTCTGGGAGA T A ENTR1 Ensembl:ENSG00000165689 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136407164..136407505 26863196 MeRIP-seq:(Medium) rs1031917792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2062177,Human_RBP_ID_27372925 Human_Splice_Rec_1099393,Human_Splice_Rec_1099409,Human_Splice_Rec_1099423,Human_Splice_Rec_1099441 RMVar_hsa_circ_51422,RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018,RMVar_hsa_circ_61004,RMVar_hsa_circ_331680 94368 RMVar_ID_94368 Human_SNP_ID_418132881 m1A Human chr9 - 136407214 136407214 136407214 TCTCCGGCCTCTCCGGCAGGGAGTCCTAGCGCAGACTTTGCGGTTCATGGAGAGTCTCTGGGAGA TCTCCGGCCTCTCCGGCAGGGAGTCCTAGCGCGGACTTTGCGGTTCATGGAGAGTCTCTGGGAGA T C ENTR1 Ensembl:ENSG00000165689 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136407164..136407505 26863196 MeRIP-seq:(Medium) rs1031917792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2062177,Human_RBP_ID_27372925 Human_Splice_Rec_1099393,Human_Splice_Rec_1099409,Human_Splice_Rec_1099423,Human_Splice_Rec_1099441 RMVar_hsa_circ_51422,RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018,RMVar_hsa_circ_61004,RMVar_hsa_circ_331680 94369 RMVar_ID_94369 Human_SNP_ID_418133633 m1A Human chr9 - 136408620 136408620 136408620 TCGGGAAGAGGGTCAGGGGGCACTGGGTCCCCAGCGTTGCAGCACCTGAGGAGCTGGTTGTTGTT TCGGGAAGAGGGTCAGGGGGCACTGGGTCCCCGGCGTTGCAGCACCTGAGGAGCTGGTTGTTGTT T C ENTR1 Ensembl:ENSG00000165689 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136408616..136408779 26863196 MeRIP-seq:(Medium) rs1036184308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9442511,Human_RBP_ID_18962566 RMVar_hsa_circ_51422,RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018 94370 RMVar_ID_94370 Human_SNP_ID_418133645 m1A Human chr9 - 136408654 136408654 136408654 AGTGGGCGTTATTTAGGCTACCTAGGTAGGAAAGTCGGGAAGAGGGTCAGGGGGCACTGGGTCCC AGTGGGCGTTATTTAGGCTACCTAGGTAGGAAGGTCGGGAAGAGGGTCAGGGGGCACTGGGTCCC T C ENTR1 Ensembl:ENSG00000165689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136408652..136408847 26863196 MeRIP-seq:(Medium) rs1002343741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9442511,Human_RBP_ID_18962566 RMVar_hsa_circ_51422,RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018 94371 RMVar_ID_94371 Human_SNP_ID_418134311 m1A Human chr9 + 136410211 136410207 136410212 CCATGGGGGCGCTCACAATTTAGCTGGGGGAGACAAGACCGGCGCTCATAGAACGCTGGAGCTGG CCATGGGGGCGCTCACAATTTAGCTGGGG_____AAGACCGGCGCTCATAGAACGCTGGAGCTGG GGAGAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:136410126..136410586;chr9:136410126..136410570 26863196 MeRIP-seq:(Medium) rs1284057354 Functional Loss DEL dbSNP153 30..34 33 - - - 94372 RMVar_ID_94372 Human_SNP_ID_418134415 m1A Human chr9 + 136410388 136410388 136410388 GGACAGCGGGGTGGCGCCCGGGCGGCGCTGGTAGCCCGACATCGCCGCCGGCCCGGCGGGGCACG GGACAGCGGGGTGGCGCCCGGGCGGCGCTGGTTGCCCGACATCGCCGCCGGCCCGGCGGGGCACG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr9:136410211..136410575;chr9:136410201..136410526 26863196,26863410 MeRIP-seq:(Medium) rs1287142292 Functional Loss SNV dbSNP153 33..33 33 - - - 94373 RMVar_ID_94373 Human_SNP_ID_418134492 m1A Human chr9 - 136410536 136410536 136410536 GCTCGGAGCGGAAGCAGCGGCGAGAGGCTCGGAGGCGCGGGGGCGGCCGAGCGGCGGGCGACGGG GCTCGGAGCGGAAGCAGCGGCGAGAGGCTCGGCGGCGCGGGGGCGGCCGAGCGGCGGGCGACGGG T G ENTR1 Ensembl:ENSG00000165689 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr9:136410069..136410625;chr9:136410416..136410600 26863196 MeRIP-seq:(Medium) rs1406279364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9339244,Human_RBP_ID_18427675 RMVar_hsa_circ_260862,RMVar_hsa_circ_114249 94374 RMVar_ID_94374 Human_SNP_ID_418134626 m1A Human chr9 - 136410700 136410700 136410700 GCGAACAGCCCCAAGAACCCGAGCCCCGCAGCAACCGCGTCGCCGCCAGCACCACAGCCGCCATC GCGAACAGCCCCAAGAACCCGAGCCCCGCAGCGACCGCGTCGCCGCCAGCACCACAGCCGCCATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136410651..136411148 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 94375 RMVar_ID_94375 Human_SNP_ID_418134627 m1A Human chr9 - 136410703 136410703 136410703 GCCGCGAACAGCCCCAAGAACCCGAGCCCCGCAGCAACCGCGTCGCCGCCAGCACCACAGCCGCC GCCGCGAACAGCCCCAAGAACCCGAGCCCCGCGGCAACCGCGTCGCCGCCAGCACCACAGCCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136410651..136410750 26863196 MeRIP-seq:(Medium) rs771285196 Functional Loss SNV dbSNP153 33..33 33 - - - 94376 RMVar_ID_94376 Human_SNP_ID_418139054 m1A Human chr9 - 136423079 136423079 136423079 TTCCGGCTTCACGTTGCCTAGTGCAGAGGGCAAACGCGTGTCACACGAGCGCGCCACGGCCCCCA TTCCGGCTTCACGTTGCCTAGTGCAGAGGGCAGACGCGTGTCACACGAGCGCGCCACGGCCCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136423073..136423187 26863196 MeRIP-seq:(Medium) rs891179314 Functional Loss SNV dbSNP153 33..33 33 - - - 94377 RMVar_ID_94377 Human_SNP_ID_418139151 m1A Human chr9 - 136423262 136423262 136423262 TCCCTGGGTCTGTCAGGCCGGGGAGCGGTTCTACCGGAAGAGCCGGTACGTCCTGGGCAGGCGCC TCCCTGGGTCTGTCAGGCCGGGGAGCGGTTCTCCCGGAAGAGCCGGTACGTCCTGGGCAGGCGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136423211..136423312 32194978 MeRIP-seq:(Medium) rs1320619683 Functional Loss SNV dbSNP153 33..33 33 - - - 94378 RMVar_ID_94378 Human_SNP_ID_418139194 m1A Human chr9 - 136423342 136423342 136423342 ACCGTTTATACAACCAGACAGCTTTTTAGACTAAATTCGTGTCCAAACTAACACGCACGGGAACG ACCGTTTATACAACCAGACAGCTTTTTAGACTCAATTCGTGTCCAAACTAACACGCACGGGAACG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136423201..136423350 32194978 MeRIP-seq:(Medium) rs762908093 Functional Loss SNV dbSNP153 33..33 33 - - - 94379 RMVar_ID_94379 Human_SNP_ID_418141740 m1A Human chr9 - 136430587 136430587 136430587 CGCTGTCCACAGGGTCTCTCCAGCGGCGAGGGACAGGCCCTGGCCCAGCTGGCCACAGACGCCAG CGCTGTCCACAGGGTCTCTCCAGCGGCGAGGGGCAGGCCCTGGCCCAGCTGGCCACAGACGCCAG T C INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136430583..136430867 26863196 MeRIP-seq:(Medium) rs915303872 Functional Loss SNV dbSNP153 33..33 33 - - - 94380 RMVar_ID_94380 Human_SNP_ID_418142184 m1A Human chr9 - 136431820 136431820 136431820 CGACCAGCTCATCCGGGAGATGCGGAAAGGTGAGGGCCTGGGGGGGCGGGCATGGAGGGAGATGA CGACCAGCTCATCCGGGAGATGCGGAAAGGTGGGGGCCTGGGGGGGCGGGCATGGAGGGAGATGA T C INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136431787..136431878 26863196 MeRIP-seq:(Medium) rs1451464457 Functional Loss SNV dbSNP153 33..33 33 - - - 94381 RMVar_ID_94381 Human_SNP_ID_418142194 m1A Human chr9 - 136431833 136431833 136431833 CGCTGCTGCAGCACGACCAGCTCATCCGGGAGATGCGGAAAGGTGAGGGCCTGGGGGGGCGGGCA CGCTGCTGCAGCACGACCAGCTCATCCGGGAGGTGCGGAAAGGTGAGGGCCTGGGGGGGCGGGCA T C INPP5E Ensembl:ENSG00000148384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136431783..136431944 26863196 MeRIP-seq:(Medium) rs768016672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099607 RMVar_hsa_circ_45444 94382 RMVar_ID_94382 Human_SNP_ID_418142432 m1A Human chr9 - 136432393 136432393 136432393 GCCCGTCGTTTTTAGGGCAGTTCTGAAGAGGCAGCGTCCTGAGCTTTGGGAAGCGAGGGCCGAAA GCCCGTCGTTTTTAGGGCAGTTCTGAAGAGGCGGCGTCCTGAGCTTTGGGAAGCGAGGGCCGAAA T C INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136431928..136432572 32194978 MeRIP-seq:(Medium) rs751058987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975136,Human_RBP_ID_9339245,Human_RBP_ID_16615958,Human_RBP_ID_22119502 RMVar_hsa_circ_45444 94383 RMVar_ID_94383 Human_SNP_ID_418142736 m1A Human chr9 + 136433072 136433072 136433072 ACACGATGCGTGTGGTCACCGTGGAGCACTCCACCTCTGTGGGAGGGGCAGCCCTCAGCTCACCT ACACGATGCGTGTGGTCACCGTGGAGCACTCCGCCTCTGTGGGAGGGGCAGCCCTCAGCTCACCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136433039..136434126 32194978 MeRIP-seq:(Medium) rs1004625981 Functional Loss SNV dbSNP153 33..33 33 - - - 94384 RMVar_ID_94384 Human_SNP_ID_418142982 m1A Human chr9 - 136433571 136433571 136433571 CGCCCACACAGGTGCTCTGGGGGAAGGAGTTGAGGTGGGCCCCACCTCCCTGGCCCATGAGTCCC CGCCCACACAGGTGCTCTGGGGGAAGGAGTTGTGGTGGGCCCCACCTCCCTGGCCCATGAGTCCC T A INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136433547..136433795 26863196 MeRIP-seq:(Medium) rs552198661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15935,Human_RBP_ID_268749,Human_RBP_ID_18468127,Human_RBP_ID_22630210 RMVar_hsa_circ_45444 94385 RMVar_ID_94385 Human_SNP_ID_418142983 m1A Human chr9 - 136433571 136433571 136433571 CGCCCACACAGGTGCTCTGGGGGAAGGAGTTGAGGTGGGCCCCACCTCCCTGGCCCATGAGTCCC CGCCCACACAGGTGCTCTGGGGGAAGGAGTTGGGGTGGGCCCCACCTCCCTGGCCCATGAGTCCC T C INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136433547..136433795 26863196 MeRIP-seq:(Medium) rs552198661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15935,Human_RBP_ID_268749,Human_RBP_ID_18468127,Human_RBP_ID_22630210 RMVar_hsa_circ_45444 94386 RMVar_ID_94386 Human_SNP_ID_418143262 m1A Human chr9 - 136434319 136434319 136434319 TCGTGCTTGGAGAGGGAAACAGGCCGAGGGCCAACGTGAGGCGTGTTTGGTGTGTCAGAGGCTGC TCGTGCTTGGAGAGGGAAACAGGCCGAGGGCCGACGTGAGGCGTGTTTGGTGTGTCAGAGGCTGC T C INPP5E Ensembl:ENSG00000148384 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136434316..136434471 26863196 MeRIP-seq:(Medium) rs878910994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906598,Human_RBP_ID_8159745,Human_RBP_ID_8944727,Human_RBP_ID_9339246,Human_RBP_ID_9442513 RMVar_hsa_circ_45444 94387 RMVar_ID_94387 Human_SNP_ID_418144628 m1A Human chr9 - 136438723 136438723 136438723 GCGCGCAGCCGCTCCTGGTGCGGGCCCACAGCAGCCTGGGCCCCGGCCGGCCGCGGAGCCCCCTG GCGCGCAGCCGCTCCTGGTGCGGGCCCACAGCGGCCTGGGCCCCGGCCGGCCGCGGAGCCCCCTG T C INPP5E Ensembl:ENSG00000148384 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136438672..136438895 26863196 MeRIP-seq:(Medium) rs1172820622 Functional Loss SNV dbSNP153 33..33 33 - - - 94388 RMVar_ID_94388 Human_SNP_ID_418144886 m1A Human chr9 - 136439178 136439178 136439178 CGCCCCGCGGCCCCCCGCCAGGCCTCGACTGGAGCGAGCCCTGTCCCTGGACGACAAGGGCTGGA CGCCCCGCGGCCCCCCGCCAGGCCTCGACTGGCGCGAGCCCTGTCCCTGGACGACAAGGGCTGGA T G INPP5E Ensembl:ENSG00000148384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136439079..136439823 26863196 MeRIP-seq:(Medium) rs1564438050 Functional Loss SNV dbSNP153 33..33 33 - - - 94389 RMVar_ID_94389 Human_SNP_ID_418144961 m1A Human chr9 - 136439319 136439319 136439319 CCAAGGACAGCTTCCCGGCGCTCCGCCGGCCCAGCGCGCGGGGTCCCCACCCGATGCTCCGGGCT CCAAGGACAGCTTCCCGGCGCTCCGCCGGCCCGGCGCGCGGGGTCCCCACCCGATGCTCCGGGCT T C INPP5E Ensembl:ENSG00000148384 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136439272..136439473 32194978 MeRIP-seq:(Medium) rs1418350214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5019857 94390 RMVar_ID_94390 Human_SNP_ID_418145052 m1A Human chr9 + 136439519 136439519 136439519 GTCCGGGGTCGCCGGCGCAGCGAGGAGCAGAAACGCCGCTGCGGCTCCCGCTTGGGCCGGGGATG GTCCGGGGTCGCCGGCGCAGCGAGGAGCAGAATCGCCGCTGCGGCTCCCGCTTGGGCCGGGGATG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136439472..136439804;chr9:136439472..136439801 26863196 MeRIP-seq:(Medium) rs1287904479 Functional Loss SNV dbSNP153 33..33 33 - - - 94391 RMVar_ID_94391 Human_SNP_ID_418145134 m1A Human chr9 + 136439760 136439759 136439761 GGTGGGAAGCGGGCACCCCTGGCTGGGCTCGCAGACTCCGAAGTCGACCCGGTACTCGCGGAGGC GGTGGGAAGCGGGCACCCCTGGCTGGGCTCGC__ACTCCGAAGTCGACCCGGTACTCGCGGAGGC CAG C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:136439671..136439773 26863410 MeRIP-seq:(Medium) rs1370903115 Functional Loss DEL dbSNP153 33..34 33 - - - 94392 RMVar_ID_94392 Human_SNP_ID_418147353 m1A Human chr9 + 136447244 136447244 136447244 GCTCGTGCTACCTACCTGGGGTTGGCACGAACAAGTTAGAAGGAATTGGGAGTGGCGCGAGTGGA GCTCGTGCTACCTACCTGGGGTTGGCACGAACCAGTTAGAAGGAATTGGGAGTGGCGCGAGTGGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136447226..136447275 26863196 MeRIP-seq:(Medium) rs1564456644 Functional Loss SNV dbSNP153 33..33 33 - - - 94393 RMVar_ID_94393 Human_SNP_ID_418147422 m1A Human chr9 - 136447363 136447363 136447363 TCACCTCAATTTGCTTCCCTCCCCTTTGCAGCAGGAACCAGAGCTCGCTACGTTGACGTCCTGAA TCACCTCAATTTGCTTCCCTCCCCTTTGCAGCGGGAACCAGAGCTCGCTACGTTGACGTCCTGAA T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136447226..136447400 26863196 MeRIP-seq:(Medium) rs1354349585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3976137,Human_RBP_ID_26240699 Human_Splice_Rec_1099662,Human_Splice_Rec_1099722,Human_Splice_Rec_1099758,Human_Splice_Rec_1099810,Human_Splice_Rec_1099866,Human_Splice_Rec_1099880,Human_Splice_Rec_1099938 Human_miRNA_ID_1095853 RMVar_hsa_circ_46101,RMVar_hsa_circ_273550,RMVar_hsa_circ_61224,RMVar_hsa_circ_308925,RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_260867,RMVar_hsa_circ_42427,RMVar_hsa_circ_260868 94394 RMVar_ID_94394 Human_SNP_ID_418147536 m1A Human chr9 - 136447675 136447675 136447675 TGTCTGAAGCTGTGTTTCCCTCTGCAGAAGAAAGCCCCGCCCCCACCTCCAACCTCGATGCCCAA TGTCTGAAGCTGTGTTTCCCTCTGCAGAAGAATGCCCCGCCCCCACCTCCAACCTCGATGCCCAA T A SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136447651..136447700 26863196 MeRIP-seq:(Medium) rs752806806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975146,Human_RBP_ID_19026085,Human_RBP_ID_22690582,Human_RBP_ID_26211494 Human_Splice_Rec_1099660,Human_Splice_Rec_1099720,Human_Splice_Rec_1099756,Human_Splice_Rec_1099808,Human_Splice_Rec_1099864,Human_Splice_Rec_1099878,Human_Splice_Rec_1099936 RMVar_hsa_circ_46101,RMVar_hsa_circ_273550,RMVar_hsa_circ_61224,RMVar_hsa_circ_308925,RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_260867,RMVar_hsa_circ_42427,RMVar_hsa_circ_260868 94395 RMVar_ID_94395 Human_SNP_ID_418147537 m1A Human chr9 - 136447675 136447675 136447675 TGTCTGAAGCTGTGTTTCCCTCTGCAGAAGAAAGCCCCGCCCCCACCTCCAACCTCGATGCCCAA TGTCTGAAGCTGTGTTTCCCTCTGCAGAAGAAGGCCCCGCCCCCACCTCCAACCTCGATGCCCAA T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136447651..136447700 26863196 MeRIP-seq:(Medium) rs752806806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975146,Human_RBP_ID_19026085,Human_RBP_ID_22690582,Human_RBP_ID_26211494 Human_Splice_Rec_1099660,Human_Splice_Rec_1099720,Human_Splice_Rec_1099756,Human_Splice_Rec_1099808,Human_Splice_Rec_1099864,Human_Splice_Rec_1099878,Human_Splice_Rec_1099936 RMVar_hsa_circ_46101,RMVar_hsa_circ_273550,RMVar_hsa_circ_61224,RMVar_hsa_circ_308925,RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_260867,RMVar_hsa_circ_42427,RMVar_hsa_circ_260868 94396 RMVar_ID_94396 Human_SNP_ID_418148637 m1A Human chr9 - 136451319 136451319 136451319 TCGGGTCCCACGCAGCCACCTCTGTCTCTCTCACCCGCTCCCGAAACAAAGAGACCCGGACAGGC TCGGGTCCCACGCAGCCACCTCTGTCTCTCTCGCCCGCTCCCGAAACAAAGAGACCCGGACAGGC T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136451251..136451425 26863196 MeRIP-seq:(Medium) rs765851297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099654,Human_Splice_Rec_1099655,Human_Splice_Rec_1099714,Human_Splice_Rec_1099715,Human_Splice_Rec_1099750,Human_Splice_Rec_1099751,Human_Splice_Rec_1099802,Human_Splice_Rec_1099803,Human_Splice_Rec_1099858,Human_Splice_Rec_1099859,Human_Splice_Rec_1099930,Human_Splice_Rec_1099931 RMVar_hsa_circ_10442,RMVar_hsa_circ_46101,RMVar_hsa_circ_308925,RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_42427,RMVar_hsa_circ_260868,RMVar_hsa_circ_61233 94397 RMVar_ID_94397 Human_SNP_ID_418153298 m1A Human chr9 - 136466124 136466124 136466124 CGTTTGCTTTGTTTTCTAAGAGTCAGATTTACAGAAGCCACAATGTGGCTGCCGGTTCCTACGAG CGTTTGCTTTGTTTTCTAAGAGTCAGATTTACGGAAGCCACAATGTGGCTGCCGGTTCCTACGAG T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136466074..136466145 26863196 MeRIP-seq:(Medium) rs1262252155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5020030 Human_Splice_Rec_1099624,Human_Splice_Rec_1099684,Human_Splice_Rec_1099772,Human_Splice_Rec_1099828,Human_Splice_Rec_1099900 RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_260868,RMVar_hsa_circ_61233,RMVar_hsa_circ_53669,RMVar_hsa_circ_336448,RMVar_hsa_circ_350779,RMVar_hsa_circ_30059,RMVar_hsa_circ_53885,RMVar_hsa_circ_65878,RMVar_hsa_circ_50592,RMVar_hsa_circ_318184,RMVar_hsa_circ_260875,RMVar_hsa_circ_316839,RMVar_hsa_circ_377985,RMVar_hsa_circ_305552 94398 RMVar_ID_94398 Human_SNP_ID_418158602 m1A Human chr9 + 136482420 136482420 136482420 AATGGCTCTGATGTTTCTGAAGGCTCTACTGTAACACTTCCATCACAAAGGGGCGAGCCGGATCA AATGGCTCTGATGTTTCTGAAGGCTCTACTGTGACACTTCCATCACAAAGGGGCGAGCCGGATCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136482410..136482487 26863196 MeRIP-seq:(Medium) rs754517158 Functional Loss SNV dbSNP153 33..33 33 - - - 94399 RMVar_ID_94399 Human_SNP_ID_418158764 m1A Human chr9 + 136482918 136482900 136482918 CTCCGCCTTCCTCCTCCCGCGCTCGCCCCCTCACCCGCGCTCGCCCCCTCACCCGCGCGGCTGAG CTCCGCCTTCCTCCT__________________CCCGCGCTCGCCCCCTCACCCGCGCGGCTGAG TCCCGCGCTCGCCCCCTCA T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:136482888..136483005 26863196 MeRIP-seq:(Medium) rs574021886 Functional Loss DEL dbSNP153 16..33 33 - - - 94400 RMVar_ID_94400 Human_SNP_ID_418158784 m1A Human chr9 + 136482936 136482936 136482936 GCGCTCGCCCCCTCACCCGCGCTCGCCCCCTCACCCGCGCGGCTGAGACCGATCCCTCAGGAGCC GCGCTCGCCCCCTCACCCGCGCTCGCCCCCTCTCCCGCGCGGCTGAGACCGATCCCTCAGGAGCC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136482842..136483021 26863196 MeRIP-seq:(Medium) rs1339070115 Functional Loss SNV dbSNP153 33..33 33 - - - 94401 RMVar_ID_94401 Human_SNP_ID_418158793 m1A Human chr9 + 136482978 136482978 136482978 CTGAGACCGATCCCTCAGGAGCCGCGGGCGAAAGCCCACCCGACGCTGGCGACGAGCACAGACAC CTGAGACCGATCCCTCAGGAGCCGCGGGCGAAGGCCCACCCGACGCTGGCGACGAGCACAGACAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136482679..136483185 26863196 MeRIP-seq:(Medium) rs1046432397 Functional Loss SNV dbSNP153 33..33 33 - - - 94402 RMVar_ID_94402 Human_SNP_ID_418158799 m1A Human chr9 + 136482988 136482988 136482988 TCCCTCAGGAGCCGCGGGCGAAAGCCCACCCGACGCTGGCGACGAGCACAGACACCTCAGCCGCC TCCCTCAGGAGCCGCGGGCGAAAGCCCACCCGGCGCTGGCGACGAGCACAGACACCTCAGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr9:136482743..136483033;chr9:136482821..136483050 26863196 MeRIP-seq:(Medium) rs1431450856 Functional Loss SNV dbSNP153 33..33 33 - - - 94403 RMVar_ID_94403 Human_SNP_ID_418158807 m1A Human chr9 + 136483005 136483005 136483005 GCGAAAGCCCACCCGACGCTGGCGACGAGCACAGACACCTCAGCCGCCGCAGCCATCTTGGCACA GCGAAAGCCCACCCGACGCTGGCGACGAGCACGGACACCTCAGCCGCCGCAGCCATCTTGGCACA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136482826..136483050 26863196 MeRIP-seq:(Medium) rs1015544532 Functional Loss SNV dbSNP153 33..33 33 - - - 94404 RMVar_ID_94404 Human_SNP_ID_418158983 m1A Human chr9 - 136483367 136483367 136483367 CGACGGGCGGGGCTAAGGGGGCGGGACGAAAGAATGAGGCGAGGAACGACGGAAGAGGGGCGGGG CGACGGGCGGGGCTAAGGGGGCGGGACGAAAGCATGAGGCGAGGAACGACGGAAGAGGGGCGGGG T G SEC16A Ensembl:ENSG00000148396 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136483329..136483429 26863196 MeRIP-seq:(Medium) rs1278848470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224320 94405 RMVar_ID_94405 Human_SNP_ID_418158984 m1A Human chr9 - 136483371 136483371 136483371 CGGACGACGGGCGGGGCTAAGGGGGCGGGACGAAAGAATGAGGCGAGGAACGACGGAAGAGGGGC CGGACGACGGGCGGGGCTAAGGGGGCGGGACGGAAGAATGAGGCGAGGAACGACGGAAGAGGGGC T C SEC16A Ensembl:ENSG00000148396 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136483321..136483423 26863196 MeRIP-seq:(Medium) rs148853824 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_539 94406 RMVar_ID_94406 Human_SNP_ID_418158989 m1A Human chr9 - 136483385 136483385 136483385 GAGGCGGAGAAAGACGGACGACGGGCGGGGCTAAGGGGGCGGGACGAAAGAATGAGGCGAGGAAC GAGGCGGAGAAAGACGGACGACGGGCGGGGCTGAGGGGGCGGGACGAAAGAATGAGGCGAGGAAC T C SEC16A Ensembl:ENSG00000148396 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136483344..136483425 26863196 MeRIP-seq:(Medium) rs1259790749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224321 94407 RMVar_ID_94407 Human_SNP_ID_418159070 m1A Human chr9 - 136483559 136483559 136483559 AAGAGCCAGCGTAAACAGGGCGACGTACTGGGACGGCCCCGGCGCGCCTGGCCGGGCAGGTGGCG AAGAGCCAGCGTAAACAGGGCGACGTACTGGGCCGGCCCCGGCGCGCCTGGCCGGGCAGGTGGCG T G SEC16A Ensembl:ENSG00000148396 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136483521..136483835 26863196 MeRIP-seq:(Medium) rs1021122955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099673 94408 RMVar_ID_94408 Human_SNP_ID_418159898 m1A Human chr9 - 136485763 136485763 136485763 GGTGCACCAGCCTGTCCTGTGTGCTCTGCATAATGTGGTACAGCAGTGGTCACAGAGCTTTGCAC GGTGCACCAGCCTGTCCTGTGTGCTCTGCATACTGTGGTACAGCAGTGGTCACAGAGCTTTGCAC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136485715..136485799 32194978 MeRIP-seq:(Medium) rs1176227218 Functional Loss SNV dbSNP153 33..33 33 - - - 94409 RMVar_ID_94409 Human_SNP_ID_418170568 m1A Human chr9 - 136515624 136515624 136515624 ACGGCTCCTGCAAGGACGGCGTCGCCACCTTCACCTGCCTCTGCCGCCCAGGCTACACGGGCCAC ACGGCTCCTGCAAGGACGGCGTCGCCACCTTCCCCTGCCTCTGCCGCCCAGGCTACACGGGCCAC T G NOTCH1 Ensembl:ENSG00000148400 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136515516..136515700 26863196 MeRIP-seq:(Medium) rs747384159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099970 Human_miRNA_ID_2272596 RMVar_hsa_circ_106844,RMVar_hsa_circ_260876,RMVar_hsa_circ_108177,RMVar_hsa_circ_260878,RMVar_hsa_circ_260882,RMVar_hsa_circ_97625,RMVar_hsa_circ_54681,RMVar_hsa_circ_291480,RMVar_hsa_circ_260884 94410 RMVar_ID_94410 Human_SNP_ID_418176421 m1A Human chr9 - 136531766 136531766 136531766 TGTCCTGGTGGTTTCCCGGGACAGGCGGGAGGAGGCGCAGGAGGGCGGCGTCTGCCCCCGGGATG TGTCCTGGTGGTTTCCCGGGACAGGCGGGAGGGGGCGCAGGAGGGCGGCGTCTGCCCCCGGGATG T C NOTCH1 Ensembl:ENSG00000148400 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136531762..136531827 26863196 MeRIP-seq:(Medium) rs1002499772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_268761,Human_RBP_ID_3908375,Human_RBP_ID_8160545,Human_RBP_ID_8224839 RMVar_hsa_circ_260876,RMVar_hsa_circ_108177,RMVar_hsa_circ_81762,RMVar_hsa_circ_260885 94411 RMVar_ID_94411 Human_SNP_ID_418178201 m1A Human chr9 - 136536356 136536356 136536356 CTAGATCCAGGCCCGTGTGACAGGAGAGAGCTAGGAACCTGGCCCCTCACTCTGAGACACAGATG CTAGATCCAGGCCCGTGTGACAGGAGAGAGCTGGGAACCTGGCCCCTCACTCTGAGACACAGATG T C NOTCH1 Ensembl:ENSG00000148400 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:136536345..136536429 26863410 MeRIP-seq:(Medium) rs1488464491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260876,RMVar_hsa_circ_108177,RMVar_hsa_circ_81762,RMVar_hsa_circ_260885 94412 RMVar_ID_94412 Human_SNP_ID_418178988 m1A Human chr9 + 136539134 136539134 136539134 GCTCTGCCCTGTGGAAGCACTTCCCCTGGTGCACTGTCTGCCCTGCCCTACCCTCTTCCTGCCAG GCTCTGCCCTGTGGAAGCACTTCCCCTGGTGCGCTGTCTGCCCTGCCCTACCCTCTTCCTGCCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136539094..136539245 26863196 MeRIP-seq:(Medium) rs919469068 Functional Loss SNV dbSNP153 33..33 33 - - - 94413 RMVar_ID_94413 Human_SNP_ID_418181041 m1A Human chr9 + 136545938 136545938 136545938 TCCCCGGCTGGCTGGCGGCGCTGTGCTCTCGCAGGCCCCCGGGCCCGGCTCCGCGCCCGGCTCGT TCCCCGGCTGGCTGGCGGCGCTGTGCTCTCGCGGGCCCCCGGGCCCGGCTCCGCGCCCGGCTCGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr9:136545717..136545982;chr9:136545866..136545962 26863196,26863410 MeRIP-seq:(Medium) rs7028061 Functional Loss SNV dbSNP153 33..33 33 - - - 94414 RMVar_ID_94414 Human_SNP_ID_418181042 m1A Human chr9 + 136545938 136545938 136545938 TCCCCGGCTGGCTGGCGGCGCTGTGCTCTCGCAGGCCCCCGGGCCCGGCTCCGCGCCCGGCTCGT TCCCCGGCTGGCTGGCGGCGCTGTGCTCTCGCTGGCCCCCGGGCCCGGCTCCGCGCCCGGCTCGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr9:136545717..136545982;chr9:136545866..136545962 26863196,26863410 MeRIP-seq:(Medium) rs7028061 Functional Loss SNV dbSNP153 33..33 33 - - - 94415 RMVar_ID_94415 Human_SNP_ID_418181247 m1A Human chr9 + 136546292 136546292 136546292 ACTACTTCTCGTTTGAAAGTTTTCAGAGGCCAAAAGTTTGAGCCGGGGCTGCGGAAGGATCCGGC ACTACTTCTCGTTTGAAAGTTTTCAGAGGCCAGAAGTTTGAGCCGGGGCTGCGGAAGGATCCGGC A G NALT1 Ensembl:ENSG00000237886 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136546255..136546395 26863196 MeRIP-seq:(Medium) rs989855753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1100055 94416 RMVar_ID_94416 Human_SNP_ID_418181268 m1A Human chr9 - 136546360 136546360 136546360 CGGGCTCCTCCGCTTATTCACATGCAAATTTCAGTCGCCAGTTGTCGCCGAGCGCGGCAACCGCC CGGGCTCCTCCGCTTATTCACATGCAAATTTCGGTCGCCAGTTGTCGCCGAGCGCGGCAACCGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136546280..136546415 26863196 MeRIP-seq:(Medium) rs776717054 Functional Loss SNV dbSNP153 33..33 33 - - - 94417 RMVar_ID_94417 Human_SNP_ID_418181796 m1A Human chr9 - 136547922 136547922 136547922 TGTGCTTCCCTCGGGCCTGTGCACCCGGCCGCACCATCCGTAACGCGGGCTTATGAGCGTGCCTG TGTGCTTCCCTCGGGCCTGTGCACCCGGCCGCGCCATCCGTAACGCGGGCTTATGAGCGTGCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136547877..136548051 26863196 MeRIP-seq:(Medium) rs1407173400 Functional Loss SNV dbSNP153 33..33 33 - - - 94418 RMVar_ID_94418 Human_SNP_ID_418219935 m1A Human chr9 + 136669688 136669688 136669688 GGCCTCGCTACGCGTGCTGCCCCGGCTGGAAGAGGACCAGCGGGCTTCCTGGGGCCTGTGGAGCA GGCCTCGCTACGCGTGCTGCCCCGGCTGGAAGCGGACCAGCGGGCTTCCTGGGGCCTGTGGAGCA A C EGFL7 Ensembl:ENSG00000172889 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136669639..136669931 32194978 MeRIP-seq:(Medium) rs776741180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23216779 Human_Splice_Rec_1100080,Human_Splice_Rec_1100081,Human_Splice_Rec_1100100,Human_Splice_Rec_1100101,Human_Splice_Rec_1100118,Human_Splice_Rec_1100119,Human_Splice_Rec_1100142,Human_Splice_Rec_1100146,Human_Splice_Rec_1100147,Human_Splice_Rec_1100160,Human_Splice_Rec_1100161 94419 RMVar_ID_94419 Human_SNP_ID_418220481 m1A Human chr9 + 136670956 136670956 136670956 GACCCAGCGCCTGGCTCTGCCCGCAGGAGTGGACAGTGCAATGAAGGAAGAAGTGCAGAGGCTGC GACCCAGCGCCTGGCTCTGCCCGCAGGAGTGGGCAGTGCAATGAAGGAAGAAGTGCAGAGGCTGC A G EGFL7 Ensembl:ENSG00000172889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136670951..136671025 32194978 MeRIP-seq:(Medium) rs746198843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961851,Human_RBP_ID_3975180,Human_RBP_ID_5228180,Human_RBP_ID_5329789,Human_RBP_ID_8944752,Human_RBP_ID_9339735,Human_RBP_ID_9341812,Human_RBP_ID_21996318,Human_RBP_ID_22630231,Human_RBP_ID_22690620,Human_RBP_ID_22748360,Human_RBP_ID_23216600,Human_RBP_ID_26361474 Human_Splice_Rec_1100086,Human_Splice_Rec_1100087,Human_Splice_Rec_1100106,Human_Splice_Rec_1100107,Human_Splice_Rec_1100124,Human_Splice_Rec_1100125,Human_Splice_Rec_1100152,Human_Splice_Rec_1100153,Human_Splice_Rec_1100166,Human_Splice_Rec_1100167 Human_miRNA_ID_550689,Human_miRNA_ID_687303,Human_miRNA_ID_889902,Human_miRNA_ID_1066478,Human_miRNA_ID_1077818,Human_miRNA_ID_2195325 RMVar_hsa_circ_78150,RMVar_hsa_circ_260891 94420 RMVar_ID_94420 Human_SNP_ID_418220516 m1A Human chr9 - 136671016 136671016 136671016 TGCCTGCCCCCCCCCCCCCCCACCAATGCCTCACCTCCTCCAGCAGGTCCACCCTGGACTGCAGC TGCCTGCCCCCCCCCCCCCCCACCAATGCCTCGCCTCCTCCAGCAGGTCCACCCTGGACTGCAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136671013..136671144 26863196 MeRIP-seq:(Medium) rs374380340 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 94421 RMVar_ID_94421 Human_SNP_ID_418220517 m1A Human chr9 - 136671016 136671016 136671016 TGCCTGCCCCCCCCCCCCCCCACCAATGCCTCACCTCCTCCAGCAGGTCCACCCTGGACTGCAGC TGCCTGCCCCCCCCCCCCCCCACCAATGCCTCCCCTCCTCCAGCAGGTCCACCCTGGACTGCAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136671013..136671144 26863196 MeRIP-seq:(Medium) rs374380340 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 94422 RMVar_ID_94422 Human_SNP_ID_418221052 m1A Human chr9 - 136672011 136672011 136672011 AGTCGATGCGGCCGAGCTGCTGGAAGGAGTGCACCAGGAGGCTGCCGGGGTCCGGGAGCCCATGC AGTCGATGCGGCCGAGCTGCTGGAAGGAGTGCGCCAGGAGGCTGCCGGGGTCCGGGAGCCCATGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136671962..136672061 32194978 MeRIP-seq:(Medium) rs980601277 Functional Loss SNV dbSNP153 33..33 33 - - - 94423 RMVar_ID_94423 Human_SNP_ID_418221227 m1A Human chr9 - 136672329 136672329 136672329 CCCAGCATGTTGGGCAGGGGCATGGGGGCTGCAGGGCGGCGTGAGGGGCTCAGTCCAGCCTGGGG CCCAGCATGTTGGGCAGGGGCATGGGGGCTGCGGGGCGGCGTGAGGGGCTCAGTCCAGCCTGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136672258..136672414 26863196 MeRIP-seq:(Medium) rs1200521577 Functional Loss SNV dbSNP153 33..33 33 - - - 94424 RMVar_ID_94424 Human_SNP_ID_418221233 m1A Human chr9 + 136672339 136672339 136672339 GACTGAGCCCCTCACGCCGCCCTGCAGCCCCCATGCCCCTGCCCAACATGCTGGGGGTCCAGAAA GACTGAGCCCCTCACGCCGCCCTGCAGCCCCCGTGCCCCTGCCCAACATGCTGGGGGTCCAGAAA A G EGFL7 Ensembl:ENSG00000172889 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136671983..136672405 26863196 MeRIP-seq:(Medium) rs1216156639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715119,Human_RBP_ID_5124271 Human_Splice_Rec_1100090,Human_Splice_Rec_1100110,Human_Splice_Rec_1100128,Human_Splice_Rec_1100170 94425 RMVar_ID_94425 Human_SNP_ID_418221333 m1A Human chr9 + 136672632 136672632 136672632 GGCCAGGCAGCCCGGAGGCTGGGTGGGGCCTCAGTGGGGGCTGCTGCCTGACCCCCAGCACAATA GGCCAGGCAGCCCGGAGGCTGGGTGGGGCCTCGGTGGGGGCTGCTGCCTGACCCCCAGCACAATA A G EGFL7 Ensembl:ENSG00000172889 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136672432..136672635 26863196 MeRIP-seq:(Medium) rs1293063680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256864,Human_RBP_ID_715130,Human_RBP_ID_5020416,Human_RBP_ID_5229535 94426 RMVar_ID_94426 Human_SNP_ID_418221694 m1A Human chr9 - 136673629 136673629 136673629 ACCACTCTGTCCGGCTCCCCCAGCTCTCACTCAGCCCGGGAAGCAGGAAGCCCCTTCTGTCACTG ACCACTCTGTCCGGCTCCCCCAGCTCTCACTCGGCCCGGGAAGCAGGAAGCCCCTTCTGTCACTG T C AGPAT2 Ensembl:ENSG00000169692 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136673579..136673706 26863196 MeRIP-seq:(Medium) rs868667663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5020442,Human_RBP_ID_26562479,Human_RBP_ID_27544340,Human_RBP_ID_27570441 RMVar_hsa_circ_95679,RMVar_hsa_circ_112519,RMVar_hsa_circ_260893,RMVar_hsa_circ_80210,RMVar_hsa_circ_89996,RMVar_hsa_circ_260894,RMVar_hsa_circ_260895,RMVar_hsa_circ_260892 94427 RMVar_ID_94427 Human_SNP_ID_418221695 m1A Human chr9 - 136673629 136673629 136673629 ACCACTCTGTCCGGCTCCCCCAGCTCTCACTCAGCCCGGGAAGCAGGAAGCCCCTTCTGTCACTG ACCACTCTGTCCGGCTCCCCCAGCTCTCACTCCGCCCGGGAAGCAGGAAGCCCCTTCTGTCACTG T G AGPAT2 Ensembl:ENSG00000169692 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136673579..136673706 26863196 MeRIP-seq:(Medium) rs868667663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5020442,Human_RBP_ID_26562479,Human_RBP_ID_27544340,Human_RBP_ID_27570441 RMVar_hsa_circ_95679,RMVar_hsa_circ_112519,RMVar_hsa_circ_260893,RMVar_hsa_circ_80210,RMVar_hsa_circ_89996,RMVar_hsa_circ_260894,RMVar_hsa_circ_260895,RMVar_hsa_circ_260892 94428 RMVar_ID_94428 Human_SNP_ID_418221774 m1A Human chr9 - 136673792 136673788 136673792 CTTCCTCCACATCTCCAAGACCCCCCAGGAGAACGGGGCCACTGCGGGGTCTGGCGTGCAGCCGG CTTCCTCCACATCTCCAAGACCCCCCAGGAGA____GGCCACTGCGGGGTCTGGCGTGCAGCCGG CCCGT C AGPAT2 Ensembl:ENSG00000169692 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136673751..136673925 26863196 MeRIP-seq:(Medium) rs1564289276 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_18132383 RMVar_hsa_circ_95679,RMVar_hsa_circ_112519,RMVar_hsa_circ_260893,RMVar_hsa_circ_80210,RMVar_hsa_circ_89996,RMVar_hsa_circ_260894,RMVar_hsa_circ_260895,RMVar_hsa_circ_260892 94429 RMVar_ID_94429 Human_SNP_ID_418222983 m1A Human chr9 + 136677017 136677017 136677017 CAGGTCGGCCATCACTGTCATGGCAGTGCTAGAGCGCTGCCGGTTGATGAAGAAGACGCCCCCGA CAGGTCGGCCATCACTGTCATGGCAGTGCTAGGGCGCTGCCGGTTGATGAAGAAGACGCCCCCGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136676951..136677075 32194978 MeRIP-seq:(Medium) rs1371561893 Functional Loss SNV dbSNP153 33..33 33 - - - 94430 RMVar_ID_94430 Human_SNP_ID_418226045 m1A Human chr9 + 136687251 136687251 136687251 CGAGCGAGGCCACGGCGGACACCGTGAAGCACAGCGCGCAGTACAGGGCGACCTTGGCGTAGAAC CGAGCGAGGCCACGGCGGACACCGTGAAGCACTGCGCGCAGTACAGGGCGACCTTGGCGTAGAAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136687201..136687323 32194978 MeRIP-seq:(Medium) rs1173020252 Functional Loss SNV dbSNP153 33..33 33 - - - 94431 RMVar_ID_94431 Human_SNP_ID_418226112 m1A Human chr9 - 136687357 136687357 136687357 GCTGGCGGCGCCGTCGGGCGCCGGGCCGGGCCATGGAGCTGTGGCCGTGTCTGGCCGCGGCGCTG GCTGGCGGCGCCGTCGGGCGCCGGGCCGGGCCGTGGAGCTGTGGCCGTGTCTGGCCGCGGCGCTG T C AGPAT2 Ensembl:ENSG00000169692 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:136687276..136687400 26863410 MeRIP-seq:(Medium) rs770394952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256300,Human_RBP_ID_5020480,Human_RBP_ID_8944670 RMVar_hsa_circ_89996,RMVar_hsa_circ_260895 94432 RMVar_ID_94432 Human_SNP_ID_418226130 m1A Human chr9 + 136687376 136687376 136687376 GGCCACAGCTCCATGGCCCGGCCCGGCGCCCGACGGCGCCGCCAGCTCGCTCCCGCTCCCGCTCC GGCCACAGCTCCATGGCCCGGCCCGGCGCCCGGCGGCGCCGCCAGCTCGCTCCCGCTCCCGCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136687281..136687385 26863196 MeRIP-seq:(Medium) rs754090246 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 94433 RMVar_ID_94433 Human_SNP_ID_418226131 m1A Human chr9 + 136687376 136687376 136687376 GGCCACAGCTCCATGGCCCGGCCCGGCGCCCGACGGCGCCGCCAGCTCGCTCCCGCTCCCGCTCC GGCCACAGCTCCATGGCCCGGCCCGGCGCCCGTCGGCGCCGCCAGCTCGCTCCCGCTCCCGCTCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136687281..136687385 26863196 MeRIP-seq:(Medium) rs754090246 Functional Loss SNV dbSNP153 33..33 33 - - - 94434 RMVar_ID_94434 Human_SNP_ID_418229066 m1A Human chr9 - 136697085 136697077 136697085 AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGGAGGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGG________GAGGAGGGGGAGGGGGGAGGAGGAG CCTCCCCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136697041..136697199 26863196 MeRIP-seq:(Medium) rs1564300270 Functional Loss DEL dbSNP153 33..40 33 - - - 94435 RMVar_ID_94435 Human_SNP_ID_418229078 m1A Human chr9 - 136697085 136697082 136697085 AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGGAGGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGG___GGGAGGAGGAGGGGGAGGGGGGAGGAGGAG CCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136697041..136697199 26863196 MeRIP-seq:(Medium) rs1564300287 Functional Loss DEL dbSNP153 33..35 33 - - - 94436 RMVar_ID_94436 Human_SNP_ID_418229080 m1A Human chr9 - 136697085 136697084 136697085 AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGGAGGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGG_GGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136697041..136697199 26863196 MeRIP-seq:(Medium) rs1564300290 Functional Loss DEL dbSNP153 33..33 33 - - - 94437 RMVar_ID_94437 Human_SNP_ID_418229081 m1A Human chr9 - 136697085 136697085 136697085 AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGGAGGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG AAGGAGGAGGGGGAGGGGGAAGGAGGAGGGGGGGGGGGAGGAGGAGGGGGAGGGGGGAGGAGGAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136697041..136697199 26863196 MeRIP-seq:(Medium) rs1317924867 Functional Loss SNV dbSNP153 33..33 33 - - - 94438 RMVar_ID_94438 Human_SNP_ID_418234729 m1A Human chr9 + 136716973 136716973 136716973 TCATTCGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTAG TCATTCGGCCAGGCACAGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCAAGGCAGGTAG A C DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1264964968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84006,RMVar_hsa_circ_260896 94439 RMVar_ID_94439 Human_SNP_ID_418235780 m1A Human chr9 + 136719718 136719718 136719718 TGGTAGGTGCCCAGGACCATGGAGGCAGCTCCATCTCCCCACCCCTGGGGGACCCTGGAGCCCCA TGGTAGGTGCCCAGGACCATGGAGGCAGCTCCGTCTCCCCACCCCTGGGGGACCCTGGAGCCCCA A G DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9411219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8159855,Human_RBP_ID_27133553 94440 RMVar_ID_94440 Human_SNP_ID_418235944 m1A Human chr9 + 136720034 136720034 136720034 CAGGGGGCTGTGTGGTCTGGGGTTCCAGGCGCAGGGGCTGGTCTGGGGCTCCGGGTGCAGGGGGC CAGGGGGCTGTGTGGTCTGGGGTTCCAGGCGCGGGGGCTGGTCTGGGGCTCCGGGTGCAGGGGGC A G DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136719988..136720224 26863196 MeRIP-seq:(Medium) rs1191942477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5330278 94441 RMVar_ID_94441 Human_SNP_ID_418235945 m1A Human chr9 + 136720060 136720034 136720061 AGGCGCAGGGGCTGGTCTGGGGCTCCGGGTGCAGGGGGCTGGTCTGGGGTTCCGGGTGCAGGGGC AGGCGCA___________________________GGGGCTGGTCTGGGGTTCCGGGTGCAGGGGC AGGGGCTGGTCTGGGGCTCCGGGTGCAG A DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136720010..136720143 26863196 MeRIP-seq:(Medium) rs1460164251 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_5330278,Human_RBP_ID_5409066 94442 RMVar_ID_94442 Human_SNP_ID_418236212 m1A Human chr9 + 136720660 136720660 136720660 GGGGGTCTGGCTAAGGAGGGGGCCTGTGGGACAGGGAAGGACAGGCCCGGAGTCATTGTGGGGCC GGGGGTCTGGCTAAGGAGGGGGCCTGTGGGACCGGGAAGGACAGGCCCGGAGTCATTGTGGGGCC A C DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4880134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8159857,Human_RBP_ID_18414458,Human_RBP_ID_22733299 GWAS_ID_12462,GWAS_ID_12463,GWAS_ID_12464,GWAS_ID_12465 94443 RMVar_ID_94443 Human_SNP_ID_418236213 m1A Human chr9 + 136720660 136720660 136720660 GGGGGTCTGGCTAAGGAGGGGGCCTGTGGGACAGGGAAGGACAGGCCCGGAGTCATTGTGGGGCC GGGGGTCTGGCTAAGGAGGGGGCCTGTGGGACTGGGAAGGACAGGCCCGGAGTCATTGTGGGGCC A T DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4880134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8159857,Human_RBP_ID_18414458,Human_RBP_ID_22733299 GWAS_ID_12462,GWAS_ID_12463,GWAS_ID_12464,GWAS_ID_12465 94444 RMVar_ID_94444 Human_SNP_ID_418237233 m1A Human chr9 + 136723116 136723116 136723116 GCGTAACGAGTTCCTGCTGCTGCTGTCCCTGCAGGAGAAGGAGCACGCCTCCAGACTGCTGGGCT GCGTAACGAGTTCCTGCTGCTGCTGTCCCTGCGGGAGAAGGAGCACGCCTCCAGACTGCTGGGCT A G DIPK1B Ensembl:ENSG00000165716 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136723066..136723165 32194978 MeRIP-seq:(Medium) rs1477453720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715154 94445 RMVar_ID_94445 Human_SNP_ID_418237636 m1A Human chr9 - 136723839 136723839 136723839 TTGCATTTCACATCTTCTGACAGGATTCCTTGAGGGAGGGTTGGACCCTGGCACCTGGCCAGCTC TTGCATTTCACATCTTCTGACAGGATTCCTTGCGGGAGGGTTGGACCCTGGCACCTGGCCAGCTC T G SNHG7 Ensembl:ENSG00000233016 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136723063..136723998 32194978 MeRIP-seq:(Medium) rs560079081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1703472,Human_RBP_ID_8276087,Human_RBP_ID_8700123,Human_RBP_ID_16616898 94446 RMVar_ID_94446 Human_SNP_ID_418237677 m1A Human chr9 + 136723950 136723950 136723950 CACCACAGACATGAGACCCCAGCTCGGAGCAAAGGCGGACATGGACATCCCGGCAGGAGAGTCCT CACCACAGACATGAGACCCCAGCTCGGAGCAACGGCGGACATGGACATCCCGGCAGGAGAGTCCT A C DIPK1B Ensembl:ENSG00000165716 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136723902..136724001 32194978 MeRIP-seq:(Medium) rs1451974965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715176,Human_RBP_ID_2062225,Human_RBP_ID_27373189,Human_RBP_ID_27544370 94447 RMVar_ID_94447 Human_SNP_ID_418238529 m1A Human chr9 - 136726373 136726373 136726373 TTTAACACGGGAAGGAGGTGACTTCGCCTGTGATGGACTTCCAGTGTGAGCACTGGCCAGAGTGA TTTAACACGGGAAGGAGGTGACTTCGCCTGTGGTGGACTTCCAGTGTGAGCACTGGCCAGAGTGA T C SNHG7 Ensembl:ENSG00000233016 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136726141..136726691 32194978 MeRIP-seq:(Medium) rs547032047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715214,Human_RBP_ID_1703484,Human_RBP_ID_2062233,Human_RBP_ID_3910910,Human_RBP_ID_5020626,Human_RBP_ID_5091000,Human_RBP_ID_5636155,Human_RBP_ID_8226179,Human_RBP_ID_8700150,Human_RBP_ID_8927407,Human_RBP_ID_9233995,Human_RBP_ID_16616955,Human_RBP_ID_18132415,Human_RBP_ID_18906043,Human_RBP_ID_19024601,Human_RBP_ID_22119521,Human_RBP_ID_22337932,Human_RBP_ID_22838209,Human_RBP_ID_24292849,Human_RBP_ID_26562496 Human_Splice_Rec_1100214,Human_Splice_Rec_1100215,Human_Splice_Rec_1100221,Human_Splice_Rec_1100225,Human_Splice_Rec_1100230,Human_Splice_Rec_1100231,Human_Splice_Rec_1100235,Human_Splice_Rec_1100240,Human_Splice_Rec_1100241 Human_miRNA_ID_2450328,Human_miRNA_ID_2450329,Human_miRNA_ID_2777462,Human_miRNA_ID_2777463,Human_miRNA_ID_3176424,Human_miRNA_ID_3195584 RMVar_hsa_circ_260897,RMVar_hsa_circ_376878,RMVar_hsa_circ_260898,RMVar_hsa_circ_349179 94448 RMVar_ID_94448 Human_SNP_ID_418243551 m1A Human chr9 + 136741944 136741944 136741944 CCACTTTGTTCACCTTTACCACGGACGCCCCCAGCTTCCTCTTGTCCCTGGCCGGCAAGAATCCC CCACTTTGTTCACCTTTACCACGGACGCCCCCGGCTTCCTCTTGTCCCTGGCCGGCAAGAATCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136740919..136741978 26863196 MeRIP-seq:(Medium) rs1238703033 Functional Loss SNV dbSNP153 33..33 33 - - - 94449 RMVar_ID_94449 Human_SNP_ID_418262107 m1A Human chr9 - 136801197 136801197 136801197 GTGCTGAGAGCCACCTGGGCTGGGACCACAGCAGGAAAAGAGCTGCGATGCAGCCTCCGTCCACC GTGCTGAGAGCCACCTGGGCTGGGACCACAGCGGGAAAAGAGCTGCGATGCAGCCTCCGTCCACC T C CCDC183-AS1,CCDC183-AS1:2,CCDC183-AS1:3,CCDC183-AS1:4,CCDC183-AS1:5,CCDC183-AS1:6,CCDC183-AS1:7,CCDC183-AS1:8,CCDC183-AS1:9 RNACentral:URS0000D59639,RNACentral:URS0000D5C9E5,RNACentral:URS0000D5BD89,RNACentral:URS0000D5824F,RNACentral:URS0000D5C11B,RNACentral:URS0000D5BD5A,RNACentral:URS0000D5B69B,RNACentral:URS00008C2725,RNACentral:URS0000D5C47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136801188..136801325 26863196 MeRIP-seq:(Medium) rs1380601757 Functional Loss SNV dbSNP153 33..33 33 - - - 94450 RMVar_ID_94450 Human_SNP_ID_418263464 m1A Human chr9 + 136804723 136804722 136804724 CAGGGCCACCACTCAGGGCCCACTCCCTGCCAAGGATGTCTCATCCCTTCCCCGCCCCCACCTCC CAGGGCCACCACTCAGGGCCCACTCCCTGCCA__GATGTCTCATCCCTTCCCCGCCCCCACCTCC AAG A CCDC183,AL355987.4,AL355987.2 Ensembl:ENSG00000213213,Ensembl:ENSG00000273066,Ensembl:ENSG00000272679 Protein coding,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136804674..136804823 26863196 MeRIP-seq:(Medium) rs754232072 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1100513,Human_Splice_Rec_1100539,Human_Splice_Rec_1100563,Human_Splice_Rec_1100575,Human_Splice_Rec_1100591,Human_Splice_Rec_1100625 RMVar_hsa_circ_126143,RMVar_hsa_circ_260902 94451 RMVar_ID_94451 Human_SNP_ID_418264586 m1A Human chr9 + 136807689 136807689 136807689 GAAGCTCAAGGCGGCCAAGAAAAAGAAGAAGTAGCCCCGCCGCCCCGCTCCCTGCTTTGCTACAC GAAGCTCAAGGCGGCCAAGAAAAAGAAGAAGTCGCCCCGCCGCCCCGCTCCCTGCTTTGCTACAC A C CCDC183,AL355987.4,AL355987.2 Ensembl:ENSG00000213213,Ensembl:ENSG00000273066,Ensembl:ENSG00000272679 Protein coding,lincRNA,lincRNA stop codon,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136807641..136807769 26863196 MeRIP-seq:(Medium) rs1240090839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9408905,Human_RBP_ID_19026128,Human_RBP_ID_26362558 94452 RMVar_ID_94452 Human_SNP_ID_418264785 m1A Human chr9 - 136808074 136808074 136808074 CGGCCCCCCCGGAGGCCGGAGCCGGCGCGGCCAGAGGCCGGGGTCCCGGCGGCGGAGCGCAGCCC CGGCCCCCCCGGAGGCCGGAGCCGGCGCGGCCGGAGGCCGGGGTCCCGGCGGCGGAGCGCAGCCC T C CCDC183-AS1 Ensembl:ENSG00000228544 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136807980..136808250 26863196 MeRIP-seq:(Medium) rs1471619047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260905,RMVar_hsa_circ_89890 94453 RMVar_ID_94453 Human_SNP_ID_418269249 m1A Human chr9 - 136821990 136821990 136821990 TGTTCATTTCCTCGCCCATCCTAGGTACCTCAACGCGCCAACTTTCAACGCCTCTGGTCATATCT TGTTCATTTCCTCGCCCATCCTAGGTACCTCAGCGCGCCAACTTTCAACGCCTCTGGTCATATCT T C CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136821984..136822222 26863196 MeRIP-seq:(Medium) rs1263285815 Functional Loss SNV dbSNP153 33..33 33 - - - 94454 RMVar_ID_94454 Human_SNP_ID_418269262 m1A Human chr9 + 136822022 136822022 136822022 TTGAGGTACCTAGGATGGGCGAGGAAATGAACAAGCTTCAGGGGAGAAGAAATGACTGTGGGAAC TTGAGGTACCTAGGATGGGCGAGGAAATGAACGAGCTTCAGGGGAGAAGAAATGACTGTGGGAAC A G AL355987.2,RABL6 Ensembl:ENSG00000272679,Ensembl:ENSG00000196642 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136822009..136822203 26863196 MeRIP-seq:(Medium) rs1473340938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5636918,Human_RBP_ID_16617341 Human_Splice_Rec_1100771,Human_Splice_Rec_1100799 RMVar_hsa_circ_260907,RMVar_hsa_circ_88767 94455 RMVar_ID_94455 Human_SNP_ID_418272575 m1A Human chr9 - 136831731 136831731 136831731 GGTGGGCACTTTTGGAAGCTCCCGGAGAATGTAATTGAAGGTCCTCGGAGAACAGGTGAGGACCT GGTGGGCACTTTTGGAAGCTCCCGGAGAATGTCATTGAAGGTCCTCGGAGAACAGGTGAGGACCT T G CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136831722..136831915 26863196 MeRIP-seq:(Medium) rs1469010047 Functional Loss SNV dbSNP153 33..33 33 - - - 94456 RMVar_ID_94456 Human_SNP_ID_418273938 m1A Human chr9 + 136835309 136835309 136835309 TTCCAGGCCAGGAGGGCAGTGGTTTGCTCCAGAGCCAGCTGCTTGTGGGTGTGGGACGGTGGCGA TTCCAGGCCAGGAGGGCAGTGGTTTGCTCCAGGGCCAGCTGCTTGTGGGTGTGGGACGGTGGCGA A G RABL6 Ensembl:ENSG00000196642 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136835292..136835425 26863196 MeRIP-seq:(Medium) rs997511308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22338115 RMVar_hsa_circ_291256,RMVar_hsa_circ_260907,RMVar_hsa_circ_88767,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260911,RMVar_hsa_circ_260912,RMVar_hsa_circ_96460,RMVar_hsa_circ_260913,RMVar_hsa_circ_260914 94457 RMVar_ID_94457 Human_SNP_ID_418273975 m1A Human chr9 - 136835430 136835427 136835430 CCCCACCCACACACGCACCTCTAAGAGTGAAGAAGCCGCACCTTCACCTGGGAAACAAAGCCCCT CCCCACCCACACACGCACCTCTAAGAGTGAAG___CCGCACCTTCACCTGGGAAACAAAGCCCCT GCTT G CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136835205..136835543 26863196 MeRIP-seq:(Medium) rs1379246232 Functional Loss DEL dbSNP153 33..35 33 - - - 94458 RMVar_ID_94458 Human_SNP_ID_418274360 m1A Human chr9 + 136836579 136836579 136836579 GCCTGGAGAGGGACCCGTGGCTTCCAGCTGCCAGGCCAGCCCCAGAATGGAGCCCCCCGCATGGG GCCTGGAGAGGGACCCGTGGCTTCCAGCTGCCCGGCCAGCCCCAGAATGGAGCCCCCCGCATGGG A C RABL6 Ensembl:ENSG00000196642 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136836572..136836651 26863196 MeRIP-seq:(Medium) rs980811468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18507264,Human_RBP_ID_22119138,Human_RBP_ID_27843763 RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913 94459 RMVar_ID_94459 Human_SNP_ID_418274458 m1A Human chr9 - 136836867 136836867 136836867 TCCATCTCAGAAAAAGAAAGAGCAGCAGTGCCAAAGGGTGGGGACAGCAGGCACCAGCGTACATG TCCATCTCAGAAAAAGAAAGAGCAGCAGTGCCTAAGGGTGGGGACAGCAGGCACCAGCGTACATG T A CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136836821..136836928 26863196 MeRIP-seq:(Medium) rs1232300753 Functional Loss SNV dbSNP153 33..33 33 - - - 94460 RMVar_ID_94460 Human_SNP_ID_418274805 m1A Human chr9 + 136837626 136837626 136837626 CACGGCGCAGCATCATCTCTAGGCTGTTTGGGACGTCACCTGCCACCGAGGCAGCCCCTCCACCT CACGGCGCAGCATCATCTCTAGGCTGTTTGGGGCGTCACCTGCCACCGAGGCAGCCCCTCCACCT A G RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136837576..136837747 26863196 MeRIP-seq:(Medium) rs1403618847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9339308,Human_RBP_ID_22338137,Human_RBP_ID_26361492,Human_RBP_ID_26833814,Human_RBP_ID_27373311 Human_Splice_Rec_1100689,Human_Splice_Rec_1100717,Human_Splice_Rec_1100743,Human_Splice_Rec_1100787,Human_Splice_Rec_1100815,Human_Splice_Rec_1100847 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_260916 94461 RMVar_ID_94461 Human_SNP_ID_418274809 m1A Human chr9 + 136837631 136837631 136837631 CGCAGCATCATCTCTAGGCTGTTTGGGACGTCACCTGCCACCGAGGCAGCCCCTCCACCTCCAGG CGCAGCATCATCTCTAGGCTGTTTGGGACGTCCCCTGCCACCGAGGCAGCCCCTCCACCTCCAGG A C RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136837580..136837705 26863196 MeRIP-seq:(Medium) rs761238208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965171,Human_RBP_ID_9339308,Human_RBP_ID_19026144,Human_RBP_ID_26361492,Human_RBP_ID_26833814 Human_Splice_Rec_1100689,Human_Splice_Rec_1100717,Human_Splice_Rec_1100743,Human_Splice_Rec_1100787,Human_Splice_Rec_1100815,Human_Splice_Rec_1100847 Human_miRNA_ID_2390233 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_260916 94462 RMVar_ID_94462 Human_SNP_ID_418275016 m1A Human chr9 - 136838017 136838017 136838017 GCAATGGGAGAGGAGGCCCAGGCCCACCCCTCACCTGTCGCTGTCCTGCTGGGCAGCCTTGGCCC GCAATGGGAGAGGAGGCCCAGGCCCACCCCTCCCCTGTCGCTGTCCTGCTGGGCAGCCTTGGCCC T G CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:136838001..136838192;chr9:136837976..136838190 26863196 MeRIP-seq:(Medium) rs1476870880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27544454 94463 RMVar_ID_94463 Human_SNP_ID_418275214 m1A Human chr9 + 136838646 136838646 136838646 CCCCGTGGCCCTGAGCTGGGCCCGCCTCCTCCACGAGCGCCCACTTGTGCGGCTCCACATCCTTC CCCCGTGGCCCTGAGCTGGGCCCGCCTCCTCCGCGAGCGCCCACTTGTGCGGCTCCACATCCTTC A G RABL6 Ensembl:ENSG00000196642 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136838638..136838717 26863196 MeRIP-seq:(Medium) rs775897585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_260916 94464 RMVar_ID_94464 Human_SNP_ID_418275607 m1A Human chr9 + 136839331 136839331 136839331 TCTCTGTTCGCACAGGTCCGGAGAAGCGCAGCAGCACCAGGCCCCCTGCTGAGATGGAGCCGGGG TCTCTGTTCGCACAGGTCCGGAGAAGCGCAGCGGCACCAGGCCCCCTGCTGAGATGGAGCCGGGG A G RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136839224..136839493 26863196 MeRIP-seq:(Medium) rs372498938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961876,Human_RBP_ID_9315405,Human_RBP_ID_9407823,Human_RBP_ID_18132459,Human_RBP_ID_24537663,Human_RBP_ID_26360532 Human_Splice_Rec_1100720,Human_Splice_Rec_1100792,Human_Splice_Rec_1100820 Human_miRNA_ID_2221565,Human_miRNA_ID_2484620,Human_miRNA_ID_3072996 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_98619,RMVar_hsa_circ_260916,RMVar_hsa_circ_260917 94465 RMVar_ID_94465 Human_SNP_ID_418275860 m1A Human chr9 - 136839790 136839790 136839790 CCCGAAGAGGTCCGAGTCATTCTTCAGTCTGAAGGCGGGGAGAGGGAGCTTGGGGGGTGGGGGCG CCCGAAGAGGTCCGAGTCATTCTTCAGTCTGAGGGCGGGGAGAGGGAGCTTGGGGGGTGGGGGCG T C CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136839751..136839800 26863196 MeRIP-seq:(Medium) rs760383497 Functional Loss SNV dbSNP153 33..33 33 - - - 94466 RMVar_ID_94466 Human_SNP_ID_418275866 m1A Human chr9 + 136839802 136839802 136839802 CCAAGCTCCCTCTCCCCGCCTTCAGACTGAAGAATGACTCGGACCTCTTCGGGCTGGGGCTGGAG CCAAGCTCCCTCTCCCCGCCTTCAGACTGAAGGATGACTCGGACCTCTTCGGGCTGGGGCTGGAG A G RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136837345..136841150 32194978 MeRIP-seq:(Medium) rs753806442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1058623,Human_RBP_ID_5020843,Human_RBP_ID_5481902,Human_RBP_ID_8700205,Human_RBP_ID_9407827 Human_Splice_Rec_1100697,Human_Splice_Rec_1100723,Human_Splice_Rec_1100751,Human_Splice_Rec_1100795,Human_Splice_Rec_1100855 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_98619,RMVar_hsa_circ_260916,RMVar_hsa_circ_260917,RMVar_hsa_circ_282976 94467 RMVar_ID_94467 Human_SNP_ID_418275892 m1A Human chr9 + 136839864 136839864 136839864 GAGGAGGCCGGACCCAAGGAGAGCAGTGAGGAAGGTGGGTGGGGGCACCAGAGTGCGGTCAGCCT GAGGAGGCCGGACCCAAGGAGAGCAGTGAGGAGGGTGGGTGGGGGCACCAGAGTGCGGTCAGCCT A G RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136839676..136839896 26863196 MeRIP-seq:(Medium) rs201227766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19144417,Human_RBP_ID_24549679 Human_Splice_Rec_1100697,Human_Splice_Rec_1100723,Human_Splice_Rec_1100751,Human_Splice_Rec_1100795,Human_Splice_Rec_1100855 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_98619,RMVar_hsa_circ_260916,RMVar_hsa_circ_260917,RMVar_hsa_circ_282976 94468 RMVar_ID_94468 Human_SNP_ID_418276187 m1A Human chr9 + 136840424 136840424 136840424 AGCGGCGACGGCGGCAGCAGCGGCCCCCGCGCAGCAGGGAGAGGACGGCTGCCGATGAGCTGGAG AGCGGCGACGGCGGCAGCAGCGGCCCCCGCGCGGCAGGGAGAGGACGGCTGCCGATGAGCTGGAG A G RABL6 Ensembl:ENSG00000196642 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:136840266..136840462 26863196 MeRIP-seq:(Medium) rs952500959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964217,Human_RBP_ID_3975190,Human_RBP_ID_5020852,Human_RBP_ID_5227514,Human_RBP_ID_9339758,Human_RBP_ID_9407830,Human_RBP_ID_17666430,Human_RBP_ID_21760776,Human_RBP_ID_21996990,Human_RBP_ID_23094438,Human_RBP_ID_24549734,Human_RBP_ID_26361501,Human_RBP_ID_27832928,Human_RBP_ID_27843948 Human_miRNA_ID_2250089,Human_miRNA_ID_2511880,Human_miRNA_ID_2570679,Human_miRNA_ID_3044425,Human_miRNA_ID_3054698 RMVar_hsa_circ_76594,RMVar_hsa_circ_78953,RMVar_hsa_circ_89237,RMVar_hsa_circ_260912,RMVar_hsa_circ_260913,RMVar_hsa_circ_98619,RMVar_hsa_circ_260916,RMVar_hsa_circ_260917 94469 RMVar_ID_94469 Human_SNP_ID_418276404 m1A Human chr9 - 136840776 136840776 136840776 TCCCTGAGAAACACTGGCGGCTCTGCCCCGAGAGGGCCAGGGTGTCCACCGAGCCTGGCTGAAGC TCCCTGAGAAACACTGGCGGCTCTGCCCCGAGGGGGCCAGGGTGTCCACCGAGCCTGGCTGAAGC T C CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136840751..136840775 26863196 MeRIP-seq:(Medium) rs1205287773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27544477 94470 RMVar_ID_94470 Human_SNP_ID_418277920 m1A Human chr9 - 136845118 136845106 136845118 AGTATGAGTCGCTGGGCGTCGGGGTGCGCGACAGCGCCATGTGGCGGGGCCCGGGCACCGTGAGG AGTATGAGTCGCTGGGCGTCGGGGTGCGCGAC____________CGGGGCCCGGGCACCGTGAGG GCCACATGGCGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:136844805..136847375;chr9:136844841..136846556;chr9:136844876..136846532 26863196 MeRIP-seq:(Medium) rs954854261 Functional Loss DEL dbSNP153 33..44 33 - - - 94471 RMVar_ID_94471 Human_SNP_ID_418278259 m1A Human chr9 - 136845690 136845690 136845690 GGGCGGACTGGTGCCGGTGCCGCCGTGCCAGGAGGCGAGCAACGGGTCGGGGTCAGAGGGCGGCA GGGCGGACTGGTGCCGGTGCCGCCGTGCCAGGTGGCGAGCAACGGGTCGGGGTCAGAGGGCGGCA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136845526..136845950 26863196 MeRIP-seq:(Medium) rs778221852 Functional Loss SNV dbSNP153 33..33 33 - - - 94472 RMVar_ID_94472 Human_SNP_ID_418278260 m1A Human chr9 - 136845690 136845690 136845690 GGGCGGACTGGTGCCGGTGCCGCCGTGCCAGGAGGCGAGCAACGGGTCGGGGTCAGAGGGCGGCA GGGCGGACTGGTGCCGGTGCCGCCGTGCCAGGCGGCGAGCAACGGGTCGGGGTCAGAGGGCGGCA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136845526..136845950 26863196 MeRIP-seq:(Medium) rs778221852 Functional Loss SNV dbSNP153 33..33 33 - - - 94473 RMVar_ID_94473 Human_SNP_ID_418279748 m1A Human chr9 + 136849187 136849185 136849187 CCCCGCTGGAGAGGAACTTCTCCGTTGGCTGGATTTCATCACCACCCATTCCCGATTCCACGTTT CCCCGCTGGAGAGGAACTTCTCCGTTGGCTG__TTTCATCACCACCCATTCCCGATTCCACGTTT GGA G PHPT1 Ensembl:ENSG00000054148 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136849042..136849231 26863196 MeRIP-seq:(Medium) rs1305468004 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5431055,Human_RBP_ID_5454316,Human_RBP_ID_5481907,Human_RBP_ID_5515873 Human_Splice_Rec_1100858 RMVar_hsa_circ_100969,RMVar_hsa_circ_260918 94474 RMVar_ID_94474 Human_SNP_ID_418279888 m1A Human chr9 + 136849425 136849425 136849425 CGGGTCGGGTGGGAGGAGGGGACTCCGGGAGGAGGAACATGGCGGTGGCGGACCTCGCTCTCATT CGGGTCGGGTGGGAGGAGGGGACTCCGGGAGGGGGAACATGGCGGTGGCGGACCTCGCTCTCATT A G PHPT1 Ensembl:ENSG00000054148 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136849401..136849425 26863196 MeRIP-seq:(Medium) rs1490132233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255729,Human_RBP_ID_846194,Human_RBP_ID_5020926,Human_RBP_ID_9442965,Human_RBP_ID_17666432,Human_RBP_ID_18472851,Human_RBP_ID_19144424,Human_RBP_ID_21996139,Human_RBP_ID_22119949,Human_RBP_ID_22467160,Human_RBP_ID_27843766 RMVar_hsa_circ_100969,RMVar_hsa_circ_260918 94475 RMVar_ID_94475 Human_SNP_ID_418279901 m1A Human chr9 - 136849438 136849438 136849438 TGTCCACATCAGGAATGAGAGCGAGGTCCGCCACCGCCATGTTCCTCCTCCCGGAGTCCCCTCCT TGTCCACATCAGGAATGAGAGCGAGGTCCGCCGCCGCCATGTTCCTCCTCCCGGAGTCCCCTCCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136849301..136849584 26863196 MeRIP-seq:(Medium) rs75735760 Functional Loss SNV dbSNP153 33..33 33 - - - 94476 RMVar_ID_94476 Human_SNP_ID_418279902 m1A Human chr9 - 136849438 136849438 136849438 TGTCCACATCAGGAATGAGAGCGAGGTCCGCCACCGCCATGTTCCTCCTCCCGGAGTCCCCTCCT TGTCCACATCAGGAATGAGAGCGAGGTCCGCCCCCGCCATGTTCCTCCTCCCGGAGTCCCCTCCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136849301..136849584 26863196 MeRIP-seq:(Medium) rs75735760 Functional Loss SNV dbSNP153 33..33 33 - - - 94477 RMVar_ID_94477 Human_SNP_ID_418279916 m1A Human chr9 - 136849447 136849447 136849447 CGGAGTCGATGTCCACATCAGGAATGAGAGCGAGGTCCGCCACCGCCATGTTCCTCCTCCCGGAG CGGAGTCGATGTCCACATCAGGAATGAGAGCGGGGTCCGCCACCGCCATGTTCCTCCTCCCGGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136849353..136849630 26863196 MeRIP-seq:(Medium) rs1230101414 Functional Loss SNV dbSNP153 33..33 33 - - - 94478 RMVar_ID_94478 Human_SNP_ID_418279922 m1A Human chr9 - 136849451 136849451 136849451 CCGTCGGAGTCGATGTCCACATCAGGAATGAGAGCGAGGTCCGCCACCGCCATGTTCCTCCTCCC CCGTCGGAGTCGATGTCCACATCAGGAATGAGTGCGAGGTCCGCCACCGCCATGTTCCTCCTCCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136849401..136849596 26863196 MeRIP-seq:(Medium) rs368087987 Functional Loss SNV dbSNP153 33..33 33 - - - 94479 RMVar_ID_94479 Human_SNP_ID_418279923 m1A Human chr9 - 136849451 136849451 136849451 CCGTCGGAGTCGATGTCCACATCAGGAATGAGAGCGAGGTCCGCCACCGCCATGTTCCTCCTCCC CCGTCGGAGTCGATGTCCACATCAGGAATGAGGGCGAGGTCCGCCACCGCCATGTTCCTCCTCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136849401..136849596 26863196 MeRIP-seq:(Medium) rs368087987 Functional Loss SNV dbSNP153 33..33 33 - - - 94480 RMVar_ID_94480 Human_SNP_ID_418279925 m1A Human chr9 + 136849455 136849455 136849455 GGAGGAACATGGCGGTGGCGGACCTCGCTCTCATTCCTGATGTGGACATCGACTCCGACGGCGTC GGAGGAACATGGCGGTGGCGGACCTCGCTCTCGTTCCTGATGTGGACATCGACTCCGACGGCGTC A G PHPT1 Ensembl:ENSG00000054148 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136849301..136849525 26863196 MeRIP-seq:(Medium) rs1185863929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715338,Human_RBP_ID_1703532,Human_RBP_ID_5020926,Human_RBP_ID_5431056,Human_RBP_ID_8700220,Human_RBP_ID_9442965,Human_RBP_ID_17666432,Human_RBP_ID_19026153,Human_RBP_ID_19146522,Human_RBP_ID_21996139,Human_RBP_ID_22119949,Human_RBP_ID_22338164,Human_RBP_ID_22467160,Human_RBP_ID_26562522 RMVar_hsa_circ_100969,RMVar_hsa_circ_260918 94481 RMVar_ID_94481 Human_SNP_ID_418279926 m1A Human chr9 + 136849455 136849455 136849455 GGAGGAACATGGCGGTGGCGGACCTCGCTCTCATTCCTGATGTGGACATCGACTCCGACGGCGTC GGAGGAACATGGCGGTGGCGGACCTCGCTCTCTTTCCTGATGTGGACATCGACTCCGACGGCGTC A T PHPT1 Ensembl:ENSG00000054148 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:136849301..136849525 26863196 MeRIP-seq:(Medium) rs1185863929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715338,Human_RBP_ID_1703532,Human_RBP_ID_5020926,Human_RBP_ID_5431056,Human_RBP_ID_8700220,Human_RBP_ID_9442965,Human_RBP_ID_17666432,Human_RBP_ID_19026153,Human_RBP_ID_19146522,Human_RBP_ID_21996139,Human_RBP_ID_22119949,Human_RBP_ID_22338164,Human_RBP_ID_22467160,Human_RBP_ID_26562522 RMVar_hsa_circ_100969,RMVar_hsa_circ_260918 94482 RMVar_ID_94482 Human_SNP_ID_418280198 m1A Human chr9 - 136849931 136849931 136849931 CGCGGGAGGAACTCCCAGCCGAAGGGGTCTGAAATCCCAGCTCTGAACAGCCCCTTCCCCAGGAG CGCGGGAGGAACTCCCAGCCGAAGGGGTCTGAGATCCCAGCTCTGAACAGCCCCTTCCCCAGGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136849929..136850208 26863196 MeRIP-seq:(Medium) rs1027250542 Functional Loss SNV dbSNP153 33..33 33 - - - 94483 RMVar_ID_94483 Human_SNP_ID_418280216 m1A Human chr9 + 136849971 136849971 136849971 CCTTCGGCTGGGAGTTCCTCCCGCGGCCTCCAAGGGCGGCCAGGGCACGTCCTGAGGCCGCCCTC CCTTCGGCTGGGAGTTCCTCCCGCGGCCTCCAGGGGCGGCCAGGGCACGTCCTGAGGCCGCCCTC A G PHPT1 Ensembl:ENSG00000054148 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136849970..136850220 26863196 MeRIP-seq:(Medium) rs766305082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5410563,Human_RBP_ID_19144426,Human_RBP_ID_22690956 RMVar_hsa_circ_100969,RMVar_hsa_circ_260918 94484 RMVar_ID_94484 Human_SNP_ID_418280713 m1A Human chr9 - 136850874 136850874 136850874 GGCAAAGGCGGGGGCTCTGAAGTGGCTGCTGGAGGCAGCAGGCCCCGGGCTGGGAGTGCTCAGTA GGCAAAGGCGGGGGCTCTGAAGTGGCTGCTGGCGGCAGCAGGCCCCGGGCTGGGAGTGCTCAGTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136850825..136850951 26863196 MeRIP-seq:(Medium) rs759701333 Functional Loss SNV dbSNP153 33..33 33 - - - 94485 RMVar_ID_94485 Human_SNP_ID_418283404 m1A Human chr9 + 136856553 136856553 136856553 GACAACGTGACCCTGAGGGACTGTAGCCCCACAGTGACCACCGAGAGAGACAGAGGTTCCTGCTG GACAACGTGACCCTGAGGGACTGTAGCCCCACGGTGACCACCGAGAGAGACAGAGGTTCCTGCTG A G MAMDC4 Ensembl:ENSG00000177943 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136856503..136856647 26863196 MeRIP-seq:(Medium) rs562832104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975203,Human_RBP_ID_5409138,Human_RBP_ID_16617566,Human_RBP_ID_19024641 Human_Splice_Rec_1100910,Human_Splice_Rec_1101014,Human_Splice_Rec_1101015 RMVar_hsa_circ_14072,RMVar_hsa_circ_108991,RMVar_hsa_circ_260921 94486 RMVar_ID_94486 Human_SNP_ID_418285862 m1A Human chr9 - 136862189 136862189 136862189 CAGTTCCGTTCTCCTCACGGGCCGAACGGAACAAGGGGTCCAGCTTGCGGGGGACCCTCCCCAGC CAGTTCCGTTCTCCTCACGGGCCGAACGGAACGAGGGGTCCAGCTTGCGGGGGACCCTCCCCAGC T C EDF1 Ensembl:ENSG00000107223 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136862101..136862400 32194978 MeRIP-seq:(Medium) rs561693227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182777,Human_RBP_ID_715355,Human_RBP_ID_1058629,Human_RBP_ID_1703551,Human_RBP_ID_17666912,Human_RBP_ID_18906127,Human_RBP_ID_26562528,Human_RBP_ID_27133912,Human_RBP_ID_27373353 Human_miRNA_ID_1134797 GWAS_ID_12466 RMVar_hsa_circ_100159,RMVar_hsa_circ_117009,RMVar_hsa_circ_124366,RMVar_hsa_circ_107067,RMVar_hsa_circ_260928,RMVar_hsa_circ_260930,RMVar_hsa_circ_88579,RMVar_hsa_circ_260931,RMVar_hsa_circ_260929,RMVar_hsa_circ_260927 94487 RMVar_ID_94487 Human_SNP_ID_418285893 m1A Human chr9 + 136862249 136862249 136862249 AACTGGCGGCCAAGGGGAACCGGCGGAACGAGATCAGCTGGAGCGCACTGATTTCGAGGCTTTGT AACTGGCGGCCAAGGGGAACCGGCGGAACGAGCTCAGCTGGAGCGCACTGATTTCGAGGCTTTGT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136862226..136862250 26863196 MeRIP-seq:(Medium) rs1564391135 Functional Loss SNV dbSNP153 33..33 33 - - - 94488 RMVar_ID_94488 Human_SNP_ID_418285922 m1A Human chr9 - 136862339 136862339 136862339 TGGCCAGTGGCTGTGGCTCATTTCAGGCCTCAAGCTCCGGGGAAAGGACATTGGAAAGCCCATCG TGGCCAGTGGCTGTGGCTCATTTCAGGCCTCAGGCTCCGGGGAAAGGACATTGGAAAGCCCATCG T C EDF1 Ensembl:ENSG00000107223 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr9:136862150..136862529;chr9:136862172..136862400 26863196 MeRIP-seq:(Medium) rs1368002372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90604,Human_RBP_ID_962431,Human_RBP_ID_5410589,Human_RBP_ID_8224357,Human_RBP_ID_9442966,Human_RBP_ID_18507268,Human_RBP_ID_22467163,Human_RBP_ID_22628937,Human_RBP_ID_26834513 Human_Splice_Rec_1101074 RMVar_hsa_circ_100159,RMVar_hsa_circ_117009,RMVar_hsa_circ_124366,RMVar_hsa_circ_107067,RMVar_hsa_circ_260928,RMVar_hsa_circ_260930,RMVar_hsa_circ_88579,RMVar_hsa_circ_260931,RMVar_hsa_circ_260929,RMVar_hsa_circ_260927 94489 RMVar_ID_94489 Human_SNP_ID_418286196 m1A Human chr9 + 136862991 136862991 136862991 CTCTCATAGTCCGCGATCACCTGTGGCTTCTCATTGATTTTCTAAAGAGAAGATGTGCTTTATAC CTCTCATAGTCCGCGATCACCTGTGGCTTCTCGTTGATTTTCTAAAGAGAAGATGTGCTTTATAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:136862901..136866275 32194978 MeRIP-seq:(Medium) rs370764238 Functional Loss SNV dbSNP153 33..33 33 - - - 94490 RMVar_ID_94490 Human_SNP_ID_418291913 m1A Human chr9 + 136882606 136882606 136882606 TGCTGGGGCTTCTCCTGAGACTGCCCGGGGACATACCCTCCCCCTGCCCCTGCTGGAGGCCTGGG TGCTGGGGCTTCTCCTGAGACTGCCCGGGGACTTACCCTCCCCCTGCCCCTGCTGGAGGCCTGGG A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136882599..136882679 26863196 MeRIP-seq:(Medium) rs1394810820 Functional Loss SNV dbSNP153 33..33 33 - - - 94491 RMVar_ID_94491 Human_SNP_ID_418293177 m1A Human chr9 - 136886594 136886582 136886594 GCGCCTGCGCCCGACCCCGCGCCCGACCCCGCACCCGACCCCGCGCCCGCGCCCGACCCCGCACC GCGCCTGCGCCCGACCCCGCGCCCGACCCCGC____________GCCCGCGCCCGACCCCGCACC CGCGGGGTCGGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136886526..136887630 26863196 MeRIP-seq:(Medium) rs1217393513 Functional Loss DEL dbSNP153 33..44 33 - - - 94492 RMVar_ID_94492 Human_SNP_ID_418293184 m1A Human chr9 - 136886594 136886594 136886594 GCGCCTGCGCCCGACCCCGCGCCCGACCCCGCACCCGACCCCGCGCCCGCGCCCGACCCCGCACC GCGCCTGCGCCCGACCCCGCGCCCGACCCCGCGCCCGACCCCGCGCCCGCGCCCGACCCCGCACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136886526..136887630 26863196 MeRIP-seq:(Medium) rs1398593872 Functional Loss SNV dbSNP153 33..33 33 - - - 94493 RMVar_ID_94493 Human_SNP_ID_418293202 m1A Human chr9 - 136886613 136886613 136886613 GTCTCCCTGAGAGGTGCCCGCGCCTGCGCCCGACCCCGCGCCCGACCCCGCACCCGACCCCGCGC GTCTCCCTGAGAGGTGCCCGCGCCTGCGCCCGCCCCCGCGCCCGACCCCGCACCCGACCCCGCGC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136886571..136886825 26863196 MeRIP-seq:(Medium) rs1217371058 Functional Loss SNV dbSNP153 33..33 33 - - - 94494 RMVar_ID_94494 Human_SNP_ID_418293212 m1A Human chr9 + 136886638 136886638 136886638 CGCGGGGTCGGGCGCAGGCGCGGGCACCTCTCAGGGAGACTCCGGGCCGGAGCGGGAGCGGGGGC CGCGGGGTCGGGCGCAGGCGCGGGCACCTCTCGGGGAGACTCCGGGCCGGAGCGGGAGCGGGGGC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:136886564..136886728 26863196 MeRIP-seq:(Medium) rs1290082769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5329806,Human_RBP_ID_8224364,Human_RBP_ID_8239114,Human_RBP_ID_9441873,Human_RBP_ID_17070601,Human_RBP_ID_18962583,Human_RBP_ID_26796870 94495 RMVar_ID_94495 Human_SNP_ID_418294425 m1A Human chr9 + 136890125 136890125 136890125 CTTGTTCAGCCGGTCACCGCGTGTGAGTCCCCACTGCACGCTCGTTCAGCCGGTCACCGTGTGTG CTTGTTCAGCCGGTCACCGCGTGTGAGTCCCCCCTGCACGCTCGTTCAGCCGGTCACCGTGTGTG A C TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136889758..136890247;chr9:136889895..136890135 26863196 MeRIP-seq:(Medium) rs367681052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617792,Human_RBP_ID_18507277,Human_RBP_ID_21996155,Human_RBP_ID_22484480,Human_RBP_ID_24292957 94496 RMVar_ID_94496 Human_SNP_ID_418294426 m1A Human chr9 + 136890125 136890125 136890125 CTTGTTCAGCCGGTCACCGCGTGTGAGTCCCCACTGCACGCTCGTTCAGCCGGTCACCGTGTGTG CTTGTTCAGCCGGTCACCGCGTGTGAGTCCCCTCTGCACGCTCGTTCAGCCGGTCACCGTGTGTG A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:136889758..136890247;chr9:136889895..136890135 26863196 MeRIP-seq:(Medium) rs367681052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617792,Human_RBP_ID_18507277,Human_RBP_ID_21996155,Human_RBP_ID_22484480,Human_RBP_ID_24292957 94497 RMVar_ID_94497 Human_SNP_ID_418294529 m1A Human chr9 + 136890413 136890413 136890413 CTTATGATACGTACAGAAAGCAAGAGCAGCCCATGCCGTCCGGCCGCGCACCAGGTCTCAGTCTG CTTATGATACGTACAGAAAGCAAGAGCAGCCCGTGCCGTCCGGCCGCGCACCAGGTCTCAGTCTG A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136890411..136890485 26863196 MeRIP-seq:(Medium) rs931287508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715381,Human_RBP_ID_5431057 Human_Splice_Rec_1101124 RMVar_hsa_circ_305064 94498 RMVar_ID_94498 Human_SNP_ID_418295764 m1A Human chr9 + 136894614 136894614 136894614 GATTGGGGGCATCATGAGGATGGAGGGGGACAAGGCCAGATGGGGCTAAACCCAGTGGCCGGGTT GATTGGGGGCATCATGAGGATGGAGGGGGACAGGGCCAGATGGGGCTAAACCCAGTGGCCGGGTT A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136894608..136894788 26863196 MeRIP-seq:(Medium) rs552579149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9441878 RMVar_hsa_circ_305064 94499 RMVar_ID_94499 Human_SNP_ID_418296759 m1A Human chr9 - 136897808 136897808 136897808 CTATAGCTACCACGGGTTCCCCTCCAGCCCCGAGAGCGGAACGTAGCACACCTGGAGCTGGCTAG CTATAGCTACCACGGGTTCCCCTCCAGCCCCGGGAGCGGAACGTAGCACACCTGGAGCTGGCTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136897804..136897872 26863196 MeRIP-seq:(Medium) rs1255919253 Functional Loss SNV dbSNP153 33..33 33 - - - 94500 RMVar_ID_94500 Human_SNP_ID_418301193 m1A Human chr9 - 136909981 136909981 136909981 GGAGGTGAAGGACACTCACCTTCTCCCGGGGGATCTTCTTCTTGCCGCAGCCGTCACAAGTTAAG GGAGGTGAAGGACACTCACCTTCTCCCGGGGGTTCTTCTTCTTGCCGCAGCCGTCACAAGTTAAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136902389..136920444 32194978 MeRIP-seq:(Medium) rs1250915147 Functional Loss SNV dbSNP153 33..33 33 - - - 94501 RMVar_ID_94501 Human_SNP_ID_418303407 m1A Human chr9 + 136916586 136916586 136916586 TCAAGACTTGTGGCAAGTGTCGAGTCCCTTGCAGATTCCACGCCATCGGCTGCCTCGAGACGGTG TCAAGACTTGTGGCAAGTGTCGAGTCCCTTGCCGATTCCACGCCATCGGCTGCCTCGAGACGGTG A C TRAF2 Ensembl:ENSG00000127191 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136916526..136916625 26863196 MeRIP-seq:(Medium) rs780369173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90844,Human_RBP_ID_964262,Human_RBP_ID_8927443,Human_RBP_ID_9315872,Human_RBP_ID_9407848,Human_RBP_ID_16618386,Human_RBP_ID_19024657 Human_Splice_Rec_1101112,Human_Splice_Rec_1101113,Human_Splice_Rec_1101140,Human_Splice_Rec_1101141,Human_Splice_Rec_1101146 RMVar_hsa_circ_5399,RMVar_hsa_circ_355760,RMVar_hsa_circ_260937,RMVar_hsa_circ_108701,RMVar_hsa_circ_335363,RMVar_hsa_circ_260940,RMVar_hsa_circ_305307,RMVar_hsa_circ_346018,RMVar_hsa_circ_107198,RMVar_hsa_circ_314815,RMVar_hsa_circ_260941,RMVar_hsa_circ_260942 94502 RMVar_ID_94502 Human_SNP_ID_418303506 m1A Human chr9 - 136916903 136916903 136916903 TGGCGAGCCGGCCGGGTACATCTGAGACGTGCACTCAACACCCAGGGAGGCTCAAGGCGACAGGT TGGCGAGCCGGCCGGGTACATCTGAGACGTGCGCTCAACACCCAGGGAGGCTCAAGGCGACAGGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:136916895..136917028 26863196 MeRIP-seq:(Medium) rs944900500 Functional Loss SNV dbSNP153 33..33 33 - - - 94503 RMVar_ID_94503 Human_SNP_ID_418304770 m1A Human chr9 + 136920388 136920388 136920388 GCTCCTGCAGAGGTGCGAGAGCCTGGAGAAGAAGACGGCCACTTTTGAGAACATTGTCTGCGTCC GCTCCTGCAGAGGTGCGAGAGCCTGGAGAAGACGACGGCCACTTTTGAGAACATTGTCTGCGTCC A C TRAF2 Ensembl:ENSG00000127191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136920183..136920515 26863196 MeRIP-seq:(Medium) rs146501200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633951,Human_RBP_ID_8930407,Human_RBP_ID_16618450 RMVar_hsa_circ_5399,RMVar_hsa_circ_260937,RMVar_hsa_circ_108701,RMVar_hsa_circ_107198,RMVar_hsa_circ_260942,RMVar_hsa_circ_260943,RMVar_hsa_circ_265791,RMVar_hsa_circ_371322 94504 RMVar_ID_94504 Human_SNP_ID_418305705 m1A Human chr9 + 136922896 136922896 136922896 GGGCCTGGGGGCACGAGGTGGAGAGGACTAGGACAGGGAGGATGGGCTTGGGGGCACGCGGTGGA GGGCCTGGGGGCACGAGGTGGAGAGGACTAGGTCAGGGAGGATGGGCTTGGGGGCACGCGGTGGA A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136922557..136923065 26863196 MeRIP-seq:(Medium) rs1181951667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3910158,Human_RBP_ID_8224372,Human_RBP_ID_19144458,Human_RBP_ID_21996160,Human_RBP_ID_22368289 RMVar_hsa_circ_260937,RMVar_hsa_circ_108701,RMVar_hsa_circ_265791 94505 RMVar_ID_94505 Human_SNP_ID_418306913 m1A Human chr9 + 136925710 136925710 136925710 TCCAGGTGACCTTAATGCTGCTCGACCAGAATAACCGGGAGCACGTGATTGACGCCTTCAGGCCC TCCAGGTGACCTTAATGCTGCTCGACCAGAATCACCGGGAGCACGTGATTGACGCCTTCAGGCCC A C TRAF2 Ensembl:ENSG00000127191 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136925676..136925725 32194978 MeRIP-seq:(Medium) rs1345029426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18906163 Human_Splice_Rec_1101120 94506 RMVar_ID_94506 Human_SNP_ID_418307079 m1A Human chr9 + 136926044 136926044 136926044 TGGGCGCTTGGGAGGGTGTCGGCCTGCAGCCAAGTTCACTGTCACGGGGGAAGGAGCCACCAGCC TGGGCGCTTGGGAGGGTGTCGGCCTGCAGCCAGGTTCACTGTCACGGGGGAAGGAGCCACCAGCC A G TRAF2 Ensembl:ENSG00000127191 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136925994..136926206 26863196 MeRIP-seq:(Medium) rs994927693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975211,Human_RBP_ID_9355132,Human_RBP_ID_18141070,Human_RBP_ID_19026228,Human_RBP_ID_22119544,Human_RBP_ID_22338209,Human_RBP_ID_22838246,Human_RBP_ID_26565633 94507 RMVar_ID_94507 Human_SNP_ID_418312059 m1A Human chr9 + 136940762 136940762 136940762 CCATCTGCACTGGCCACCCCGTGCCAAGCATCACAGCTGCGTGAGCAGGTTTGTGTGTGAGCGTG CCATCTGCACTGGCCACCCCGTGCCAAGCATCGCAGCTGCGTGAGCAGGTTTGTGTGTGAGCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136940711..136940863 26863196 MeRIP-seq:(Medium) rs1315137200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8700378 94508 RMVar_ID_94508 Human_SNP_ID_418312228 m1A Human chr9 - 136941034 136941034 136941034 GGAGCAGGAGCTGCTGCTCACGGCCAGCGACGACGCCACCATCAAAGCCTGGCGCTCCCCACGCA GGAGCAGGAGCTGCTGCTCACGGCCAGCGACGCCGCCACCATCAAAGCCTGGCGCTCCCCACGCA T G FBXW5 Ensembl:ENSG00000159069 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136940985..136941173 26863196 MeRIP-seq:(Medium) rs762147399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256176 RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947 94509 RMVar_ID_94509 Human_SNP_ID_418312240 m1A Human chr9 + 136941052 136941052 136941052 CTTTGATGGTGGCGTCGTCGCTGGCCGTGAGCAGCAGCTCCTGCTCCTGGGGACTGAAGACCACT CTTTGATGGTGGCGTCGTCGCTGGCCGTGAGCGGCAGCTCCTGCTCCTGGGGACTGAAGACCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136941003..136941114 26863196 MeRIP-seq:(Medium) rs747602415 Functional Loss SNV dbSNP153 33..33 33 - - - 94510 RMVar_ID_94510 Human_SNP_ID_418312270 m1A Human chr9 - 136941100 136941100 136941100 CTACAACATCTGTCTGGCCAGGCTGCGGCACGAGGATGTGGTCAACTCAGTGGTCTTCAGTCCCC CTACAACATCTGTCTGGCCAGGCTGCGGCACGCGGATGTGGTCAACTCAGTGGTCTTCAGTCCCC T G FBXW5 Ensembl:ENSG00000159069 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136941051..136941150 32194978 MeRIP-seq:(Medium) rs766798323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715420,Human_RBP_ID_18197222,Human_RBP_ID_18906180,Human_RBP_ID_22119152,Human_RBP_ID_27544557 Human_Splice_Rec_1101156,Human_Splice_Rec_1101170,Human_Splice_Rec_1101182,Human_Splice_Rec_1101198 RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947 94511 RMVar_ID_94511 Human_SNP_ID_418312656 m1A Human chr9 + 136941610 136941610 136941610 TATGTCTATGACGTGGTCCAGCGCGTCGAAGAAGGCATCGGAGCCCCGGCCCTCACCCAGCACGG TATGTCTATGACGTGGTCCAGCGCGTCGAAGACGGCATCGGAGCCCCGGCCCTCACCCAGCACGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136941574..136941668 26863196 MeRIP-seq:(Medium) rs34563315 Functional Loss SNV dbSNP153 33..33 33 - - - 94512 RMVar_ID_94512 Human_SNP_ID_418312931 m1A Human chr9 - 136942133 136942108 136942134 AGGTGGCCGAGCTGCTGGCCCAGGGCCACACCAAGCCACCCGAGCGCAGTGCCACAGGCGCCAAG AGGTGGCCGAGCTGCTGGCCCAGGGCCACAC__________________________GCGCCAAG CCTGTGGCACTGCGCTCGGGTGGCTTG C FBXW5 Ensembl:ENSG00000159069 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136942082..136942214 26863196 MeRIP-seq:(Medium) rs1564434080 Functional Loss DEL dbSNP153 32..57 33 - - - Human_Splice_Rec_1101165,Human_Splice_Rec_1101193,Human_Splice_Rec_1101205 RMVar_hsa_circ_81707,RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947,RMVar_hsa_circ_260948 94513 RMVar_ID_94513 Human_SNP_ID_418313130 m1A Human chr9 - 136942391 136942391 136942391 AGATCCAGAACCTCAATGCCAGCACCGTCCGCACGGTGATGGTGGCCGACTGCAGCCGCTTCGAC AGATCCAGAACCTCAATGCCAGCACCGTCCGCGCGGTGATGGTGGCCGACTGCAGCCGCTTCGAC T C FBXW5 Ensembl:ENSG00000159069 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136941983..136942501 26863196 MeRIP-seq:(Medium) rs1264926854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1101150,Human_Splice_Rec_1101178,Human_Splice_Rec_1101192,Human_Splice_Rec_1101204 RMVar_hsa_circ_81707,RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947,RMVar_hsa_circ_260948 94514 RMVar_ID_94514 Human_SNP_ID_418313886 m1A Human chr9 + 136943393 136943393 136943393 GTCCTTGGAGCAGGACGCGAACTGGTACCCGGAATGGGAGAAGCTGAGGTGCAGGACCTGGTCTG GTCCTTGGAGCAGGACGCGAACTGGTACCCGGCATGGGAGAAGCTGAGGTGCAGGACCTGGTCTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136943351..136944050 32194978 MeRIP-seq:(Medium) rs1313360763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16619156 94515 RMVar_ID_94515 Human_SNP_ID_418313936 m1A Human chr9 - 136943470 136943470 136943470 CATGTCCTGGTACGAGGAGTTCCAGCGGCTGTATGACACGGTGCCCTGCGTGGAGGTGCAGACGC CATGTCCTGGTACGAGGAGTTCCAGCGGCTGTGTGACACGGTGCCCTGCGTGGAGGTGCAGACGC T C FBXW5 Ensembl:ENSG00000159069 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136943419..136943520 26863196 MeRIP-seq:(Medium) rs1467765628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797740,Human_RBP_ID_962436,Human_RBP_ID_5041281,Human_RBP_ID_19026237 Human_Splice_Rec_1101160,Human_Splice_Rec_1101174,Human_Splice_Rec_1101186,Human_Splice_Rec_1101200,Human_Splice_Rec_1101212,Human_Splice_Rec_1101220,Human_Splice_Rec_1101226 RMVar_hsa_circ_117139,RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947,RMVar_hsa_circ_345205,RMVar_hsa_circ_260954,RMVar_hsa_circ_86422,RMVar_hsa_circ_260955,RMVar_hsa_circ_260953 94516 RMVar_ID_94516 Human_SNP_ID_418314369 m1A Human chr9 - 136944086 136944086 136944086 GGTGGGTTTCAGGGCCGCCTGGGCAGAATGTCACGATGGACGAGGGCGGCACGCCCCTGCTCCCC GGTGGGTTTCAGGGCCGCCTGGGCAGAATGTCGCGATGGACGAGGGCGGCACGCCCCTGCTCCCC T C FBXW5 Ensembl:ENSG00000159069 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:136943880..136944155;chr9:136943898..136944150;chr9:136943969..136944291 26863196 MeRIP-seq:(Medium) rs980009644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964270,Human_RBP_ID_5036598,Human_RBP_ID_18197227,Human_RBP_ID_22556862,Human_RBP_ID_23259619 Human_Splice_Rec_1101158,Human_Splice_Rec_1101172,Human_Splice_Rec_1101184,Human_Splice_Rec_1101210,Human_Splice_Rec_1101218 RMVar_hsa_circ_117139,RMVar_hsa_circ_100040,RMVar_hsa_circ_260947,RMVar_hsa_circ_260954,RMVar_hsa_circ_86422,RMVar_hsa_circ_260955 94517 RMVar_ID_94517 Human_SNP_ID_418314423 m1A Human chr9 - 136944213 136944213 136944213 CGGCGGTACCCGGGCGTCCCCTGCAGACACGCAGCCCCGTGGAACTCCCGGCGGGACGGTTGGGG CGGCGGTACCCGGGCGTCCCCTGCAGACACGCGGCCCCGTGGAACTCCCGGCGGGACGGTTGGGG T C FBXW5 Ensembl:ENSG00000159069 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136944210..136944309 26863196 MeRIP-seq:(Medium) rs999961843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5409162 RMVar_hsa_circ_100040,RMVar_hsa_circ_260947,RMVar_hsa_circ_86422,RMVar_hsa_circ_260955 94518 RMVar_ID_94518 Human_SNP_ID_418314520 m1A Human chr9 + 136944415 136944415 136944415 ACCAGGCGCCGTCCGGGGACGGGCTTCCGCCGAGAGGAAGCTCGGGGCGGCCAGGCAGTGGCCTC ACCAGGCGCCGTCCGGGGACGGGCTTCCGCCGGGAGGAAGCTCGGGGCGGCCAGGCAGTGGCCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:136944413..136944728 26863196 MeRIP-seq:(Medium) rs993434670 Functional Loss SNV dbSNP153 33..33 33 - - - 94519 RMVar_ID_94519 Human_SNP_ID_418316756 m1A Human chr9 - 136949581 136949581 136949581 CTCCCCTCTCTCTTCCCACTCTCCGGGCAAAGACCTTTTCCCAGACACGGTCCTGGGCGCTGGGA CTCCCCTCTCTCTTCCCACTCTCCGGGCAAAGGCCTTTTCCCAGACACGGTCCTGGGCGCTGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136949579..136949842 26863196 MeRIP-seq:(Medium) rs1474297947 Functional Loss SNV dbSNP153 33..33 33 - - - 94520 RMVar_ID_94520 Human_SNP_ID_418319560 m1A Human chr9 + 136957686 136957686 136957686 GAAGGGTGGGTGGATGGATAGTTGGATGGATGATGCTTTTTTGCTCTTTTTTTCTTGTGCCCTAG GAAGGGTGGGTGGATGGATAGTTGGATGGATGGTGCTTTTTTGCTCTTTTTTTCTTGTGCCCTAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136957637..136957764 26863196 MeRIP-seq:(Medium) rs1038204139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3908414,Human_RBP_ID_8225637 94521 RMVar_ID_94521 Human_SNP_ID_418319902 m1A Human chr9 + 136959096 136959086 136959096 CTGGGAGCTGGCGGCGTGGAGCCGAGGCCAGGAGAGGCCAGGCAGGTGGTCCAGGCATGTCTGCC CTGGGAGCTGGCGGCGTGGAGCC__________GAGGCCAGGCAGGTGGTCCAGGCATGTCTGCC CGAGGCCAGGA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136959046..136959270 26863196 MeRIP-seq:(Medium) rs997489224 Functional Loss DEL dbSNP153 24..33 33 - - - 94522 RMVar_ID_94522 Human_SNP_ID_418320344 m1A Human chr9 - 136960602 136960575 136960602 ACCCTCGCCCCCGGCCACAGAACATTCTACCCACCCCGCAGCTGCAGGCTGTACCCTCACCCTGG ACCCTCGCCCCCGGCCACAGAACATTCTACCC___________________________CCCTGG GTGAGGGTACAGCCTGCAGCTGCGGGGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136960526..136960655 26863196 MeRIP-seq:(Medium) rs1444291053 Functional Loss DEL dbSNP153 33..59 33 - - - 94523 RMVar_ID_94523 Human_SNP_ID_418320355 m1A Human chr9 - 136960602 136960602 136960602 ACCCTCGCCCCCGGCCACAGAACATTCTACCCACCCCGCAGCTGCAGGCTGTACCCTCACCCTGG ACCCTCGCCCCCGGCCACAGAACATTCTACCCCCCCCGCAGCTGCAGGCTGTACCCTCACCCTGG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136960526..136960655 26863196 MeRIP-seq:(Medium) rs865995636 Functional Loss SNV dbSNP153 33..33 33 - - - 94524 RMVar_ID_94524 Human_SNP_ID_418325640 m1A Human chr9 - 136978283 136978283 136978283 CCGATTCTGTGCCCTGGCTGAGCGCCTGGCCCATACAGCGGGCGGCAGAGGACGTCGCATTCCTG CCGATTCTGTGCCCTGGCTGAGCGCCTGGCCCGTACAGCGGGCGGCAGAGGACGTCGCATTCCTG T C lnc-CLIC3-4 RNACentral:URS00009C172E lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136978274..136978373 26863196 MeRIP-seq:(Medium) rs1395307113 Functional Loss SNV dbSNP153 33..33 33 - - - 94525 RMVar_ID_94525 Human_SNP_ID_418325641 m1A Human chr9 - 136978283 136978283 136978283 CCGATTCTGTGCCCTGGCTGAGCGCCTGGCCCATACAGCGGGCGGCAGAGGACGTCGCATTCCTG CCGATTCTGTGCCCTGGCTGAGCGCCTGGCCCCTACAGCGGGCGGCAGAGGACGTCGCATTCCTG T G lnc-CLIC3-4 RNACentral:URS00009C172E lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136978274..136978373 26863196 MeRIP-seq:(Medium) rs1395307113 Functional Loss SNV dbSNP153 33..33 33 - - - 94526 RMVar_ID_94526 Human_SNP_ID_418326017 m1A Human chr9 + 136978954 136978954 136978954 GCGCCCCCGCAGGTAGGCGCAGGTGGGTCCGGAGGGTCCTGGCCGACGCGGGTGGGGGTCGCTCG GCGCCCCCGCAGGTAGGCGCAGGTGGGTCCGGCGGGTCCTGGCCGACGCGGGTGGGGGTCGCTCG A C AL807752.7,PTGDS Ensembl:ENSG00000284341,Ensembl:ENSG00000107317 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136978950..136979087 26863196 MeRIP-seq:(Medium) rs768517023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5124281,Human_RBP_ID_23216788 94527 RMVar_ID_94527 Human_SNP_ID_418330130 m1A Human chr9 - 136992475 136992474 136992475 ACACGAAGCGGGGCGGCTCGGGGCCCGGCGGCAGCGTGCAGAGCGGCGGCGACAGCGGATCCATG ACACGAAGCGGGGCGGCTCGGGGCCCGGCGGC_GCGTGCAGAGCGGCGGCGACAGCGGATCCATG CT C lnc-CLIC3-1-001 RNACentral:URS00009AD959 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136992426..136992650 26863196 MeRIP-seq:(Medium) rs1382550718 Functional Loss DEL dbSNP153 33..33 33 - - - 94528 RMVar_ID_94528 Human_SNP_ID_418330168 m1A Human chr9 + 136992541 136992541 136992541 CTACTGCGAAGGGGAGGAAAGCGGGGAGGGGGACCGCGGCGGCTTCAACCTCTAGTGAGTGGGGG CTACTGCGAAGGGGAGGAAAGCGGGGAGGGGGGCCGCGGCGGCTTCAACCTCTAGTGAGTGGGGG A G PAXX Ensembl:ENSG00000148362 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:136992450..136992628 26863410 MeRIP-seq:(Medium) rs576291300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256136,Human_RBP_ID_5021219,Human_RBP_ID_5124285,Human_RBP_ID_18132537 Human_Splice_Rec_1101467,Human_Splice_Rec_1101483,Human_Splice_Rec_1101491,Human_Splice_Rec_1101499 Human_miRNA_ID_3010562 RMVar_hsa_circ_92680,RMVar_hsa_circ_260957,RMVar_hsa_circ_82681,RMVar_hsa_circ_260956 94529 RMVar_ID_94529 Human_SNP_ID_418330177 m1A Human chr9 - 136992564 136992564 136992564 CTGCACCCCTACCTCCCCGCGGACCCCCACTCACTAGAGGTTGAAGCCGCCGCGGTCCCCCTCCC CTGCACCCCTACCTCCCCGCGGACCCCCACTCGCTAGAGGTTGAAGCCGCCGCGGTCCCCCTCCC T C lnc-CLIC3-1-001 RNACentral:URS00009AD959 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:136992465..136992629;chr9:136992401..136992801;chr9:136992401..136992753 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1404167187 Functional Loss SNV dbSNP153 33..33 33 - - - 94530 RMVar_ID_94530 Human_SNP_ID_418330178 m1A Human chr9 - 136992564 136992564 136992564 CTGCACCCCTACCTCCCCGCGGACCCCCACTCACTAGAGGTTGAAGCCGCCGCGGTCCCCCTCCC CTGCACCCCTACCTCCCCGCGGACCCCCACTCCCTAGAGGTTGAAGCCGCCGCGGTCCCCCTCCC T G lnc-CLIC3-1-001 RNACentral:URS00009AD959 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,Starvation treatment;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:136992465..136992629;chr9:136992401..136992801;chr9:136992401..136992753 26863410,26863196,26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 94531 RMVar_ID_94531 Human_SNP_ID_418330394 m1A Human chr9 + 136993119 136993119 136993119 CTGCAGGAGGACAGAGCATCCCTGACGCTTTCAGGGGGGCCCTCGGCACTGGCCTTTGACCTCTC CTGCAGGAGGACAGAGCATCCCTGACGCTTTCGGGGGGGCCCTCGGCACTGGCCTTTGACCTCTC A G PAXX Ensembl:ENSG00000148362 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136992848..136993181 26863196 MeRIP-seq:(Medium) rs1293084528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715440,Human_RBP_ID_796988,Human_RBP_ID_1058641,Human_RBP_ID_5021239,Human_RBP_ID_5431061,Human_RBP_ID_5481922,Human_RBP_ID_5515882,Human_RBP_ID_18132540,Human_RBP_ID_19147236,Human_RBP_ID_23094574 Human_Splice_Rec_1101472,Human_Splice_Rec_1101480,Human_Splice_Rec_1101502,Human_Splice_Rec_1101518 Human_miRNA_ID_2295460,Human_miRNA_ID_2452219,Human_miRNA_ID_2515783,Human_miRNA_ID_2700860 RMVar_hsa_circ_92680,RMVar_hsa_circ_102136,RMVar_hsa_circ_260957,RMVar_hsa_circ_260958 94532 RMVar_ID_94532 Human_SNP_ID_418330446 m1A Human chr9 + 136993236 136993235 136993236 CTGGCAAAACGCGTGTGGAGCCTGGAGCGGCGACTGGCAGGTAGGATTGGGGGTGGGCACCTCAT CTGGCAAAACGCGTGTGGAGCCTGGAGCGGCG_CTGGCAGGTAGGATTGGGGGTGGGCACCTCAT GA G PAXX Ensembl:ENSG00000148362 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr9:136992866..136993252;chr9:136992515..136993444 26863196,32194978 MeRIP-seq:(Medium) rs1409478773 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_19024665,Human_RBP_ID_23094576 Human_Splice_Rec_1101473,Human_Splice_Rec_1101481,Human_Splice_Rec_1101485,Human_Splice_Rec_1101493,Human_Splice_Rec_1101503,Human_Splice_Rec_1101511,Human_Splice_Rec_1101519 RMVar_hsa_circ_92680,RMVar_hsa_circ_102136,RMVar_hsa_circ_260957,RMVar_hsa_circ_260958 94533 RMVar_ID_94533 Human_SNP_ID_418330450 m1A Human chr9 + 136993236 136993236 136993236 CTGGCAAAACGCGTGTGGAGCCTGGAGCGGCGACTGGCAGGTAGGATTGGGGGTGGGCACCTCAT CTGGCAAAACGCGTGTGGAGCCTGGAGCGGCGGCTGGCAGGTAGGATTGGGGGTGGGCACCTCAT A G PAXX Ensembl:ENSG00000148362 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr9:136992866..136993252;chr9:136992515..136993444 26863196,32194978 MeRIP-seq:(Medium) rs1176237713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19024665,Human_RBP_ID_23094576 Human_Splice_Rec_1101473,Human_Splice_Rec_1101481,Human_Splice_Rec_1101485,Human_Splice_Rec_1101493,Human_Splice_Rec_1101503,Human_Splice_Rec_1101511,Human_Splice_Rec_1101519 RMVar_hsa_circ_92680,RMVar_hsa_circ_102136,RMVar_hsa_circ_260957,RMVar_hsa_circ_260958 94534 RMVar_ID_94534 Human_SNP_ID_418330455 m1A Human chr9 - 136993245 136993245 136993245 AGTGAAGGTATGAGGTGCCCACCCCCAATCCTACCTGCCAGTCGCCGCTCCAGGCTCCACACGCG AGTGAAGGTATGAGGTGCCCACCCCCAATCCTCCCTGCCAGTCGCCGCTCCAGGCTCCACACGCG T G lnc-CLIC3-1-001 RNACentral:URS00009AD959 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:136993151..136993444 26863410 MeRIP-seq:(Medium) rs775689767 Functional Loss SNV dbSNP153 33..33 33 - - - 94535 RMVar_ID_94535 Human_SNP_ID_418331360 m1A Human chr9 - 136995511 136995509 136995511 CGCCCCCGGCTCGCAGCTGCCCATCCTGCTCTATGACAGCGACGCCAAGACAGACACGCTGCAGA CGCCCCCGGCTCGCAGCTGCCCATCCTGCTCT__GACAGCGACGCCAAGACAGACACGCTGCAGA CAT C CLIC3 Ensembl:ENSG00000169583 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136995431..136995746 26863196 MeRIP-seq:(Medium) rs776176446 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1101528,Human_Splice_Rec_1101529,Human_Splice_Rec_1101536,Human_Splice_Rec_1101537,Human_Splice_Rec_1101543 94536 RMVar_ID_94536 Human_SNP_ID_418331363 m1A Human chr9 - 136995511 136995511 136995511 CGCCCCCGGCTCGCAGCTGCCCATCCTGCTCTATGACAGCGACGCCAAGACAGACACGCTGCAGA CGCCCCCGGCTCGCAGCTGCCCATCCTGCTCTGTGACAGCGACGCCAAGACAGACACGCTGCAGA T C CLIC3 Ensembl:ENSG00000169583 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136995431..136995746 26863196 MeRIP-seq:(Medium) rs1461438409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1101528,Human_Splice_Rec_1101529,Human_Splice_Rec_1101536,Human_Splice_Rec_1101537,Human_Splice_Rec_1101543 94537 RMVar_ID_94537 Human_SNP_ID_418331478 m1A Human chr9 + 136995735 136995735 136995735 TGAAGAGCCGCTGGCAGGAGGGGCAGTGACCCACGCTCTCCCCGTCCTCACTCGCCTGGGTGGGT TGAAGAGCCGCTGGCAGGAGGGGCAGTGACCCTCGCTCTCCCCGTCCTCACTCGCCTGGGTGGGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136995633..136995735 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 94538 RMVar_ID_94538 Human_SNP_ID_418335891 m1A Human chr9 + 137009298 137009298 137009298 CCCACAGCCCTCACAGCCCTGCAGCCACCCCCACTCCTGGCCCCGCTGCCTGGCCGCCCCCCCCG CCCACAGCCCTCACAGCCCTGCAGCCACCCCCCCTCCTGGCCCCGCTGCCTGGCCGCCCCCCCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137009289..137009440 26863196 MeRIP-seq:(Medium) rs1191399750 Functional Loss SNV dbSNP153 33..33 33 - - - 94539 RMVar_ID_94539 Human_SNP_ID_418336054 m1A Human chr9 - 137009616 137009616 137009616 CCAGGACGAGCCCACCACAGGCATGGACCCCAAGGCCCGGCGCTTCCTCTGGAACCTCATCCTTG CCAGGACGAGCCCACCACAGGCATGGACCCCAGGGCCCGGCGCTTCCTCTGGAACCTCATCCTTG T C ABCA2 Ensembl:ENSG00000107331 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137009500..137009656 26863196 MeRIP-seq:(Medium) rs1389843121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8927479 Human_Splice_Rec_1101634,Human_Splice_Rec_1101635,Human_Splice_Rec_1101726,Human_Splice_Rec_1101727,Human_Splice_Rec_1101820,Human_Splice_Rec_1101821,Human_Splice_Rec_1101912,Human_Splice_Rec_1101913,Human_Splice_Rec_1101980,Human_Splice_Rec_1101981,Human_Splice_Rec_1102072,Human_Splice_Rec_1102073,Human_Splice_Rec_1102164,Human_Splice_Rec_1102165,Human_Splice_Rec_1102181,Human_Splice_Rec_1102200,Human_Splice_Rec_1102201,Human_Splice_Rec_1102206,Human_Splice_Rec_1102207 Human_miRNA_ID_594993,Human_miRNA_ID_1606507,Human_miRNA_ID_1680759 RMVar_hsa_circ_43507,RMVar_hsa_circ_31859 94540 RMVar_ID_94540 Human_SNP_ID_418336166 m1A Human chr9 + 137009902 137009902 137009902 TCAGCTCCAGCTTCTCCAGAGCCCACTTCACCACCTGGCCAGGGAACGCAGGTGTCAGTGGAGGC TCAGCTCCAGCTTCTCCAGAGCCCACTTCACCTCCTGGCCAGGGAACGCAGGTGTCAGTGGAGGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137009900..137010012 32194978 MeRIP-seq:(Medium) rs1281815541 Functional Loss SNV dbSNP153 33..33 33 - - - 94541 RMVar_ID_94541 Human_SNP_ID_418337833 m1A Human chr9 + 137013316 137013316 137013316 GCTGCTGGGGGCTGGCGTCGGGCGATAGCCGCAGCCTGCGGGCACCGACAGTGTGAGGTGGGGCT GCTGCTGGGGGCTGGCGTCGGGCGATAGCCGCGGCCTGCGGGCACCGACAGTGTGAGGTGGGGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137013053..137013336 26863196 MeRIP-seq:(Medium) rs756430995 Functional Loss SNV dbSNP153 33..33 33 - - - 94542 RMVar_ID_94542 Human_SNP_ID_418337834 m1A Human chr9 + 137013316 137013316 137013316 GCTGCTGGGGGCTGGCGTCGGGCGATAGCCGCAGCCTGCGGGCACCGACAGTGTGAGGTGGGGCT GCTGCTGGGGGCTGGCGTCGGGCGATAGCCGCTGCCTGCGGGCACCGACAGTGTGAGGTGGGGCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137013053..137013336 26863196 MeRIP-seq:(Medium) rs756430995 Functional Loss SNV dbSNP153 33..33 33 - - - 94543 RMVar_ID_94543 Human_SNP_ID_418338077 m1A Human chr9 - 137013813 137013812 137013813 CGTCCCGGAGATTGGTAGGCCACCGGCTGGACAGGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG CGTCCCGGAGATTGGTAGGCCACCGGCTGGAC_GGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG CT C ABCA2 Ensembl:ENSG00000107331 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137013810..137013972 26863196 MeRIP-seq:(Medium) rs1205925236 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_46620 94544 RMVar_ID_94544 Human_SNP_ID_418338078 m1A Human chr9 - 137013813 137013813 137013813 CGTCCCGGAGATTGGTAGGCCACCGGCTGGACAGGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG CGTCCCGGAGATTGGTAGGCCACCGGCTGGACTGGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG T A ABCA2 Ensembl:ENSG00000107331 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137013810..137013972 26863196 MeRIP-seq:(Medium) rs10781531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46620 94545 RMVar_ID_94545 Human_SNP_ID_418338079 m1A Human chr9 - 137013813 137013813 137013813 CGTCCCGGAGATTGGTAGGCCACCGGCTGGACAGGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG CGTCCCGGAGATTGGTAGGCCACCGGCTGGACGGGGGTGCTGGGCTTGCCTCCCCCCACCGCCCG T C ABCA2 Ensembl:ENSG00000107331 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137013810..137013972 26863196 MeRIP-seq:(Medium) rs10781531 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_46620 94546 RMVar_ID_94546 Human_SNP_ID_418338463 m1A Human chr9 + 137014667 137014667 137014667 CCGAGCTGGGGCCTTGTGGGTGGGGTGGGCTGAGCAAGTGGTCCAGGCCCCTCACCGGCCTCACT CCGAGCTGGGGCCTTGTGGGTGGGGTGGGCTGGGCAAGTGGTCCAGGCCCCTCACCGGCCTCACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137014665..137014746 26863196 MeRIP-seq:(Medium) rs1424267015 Functional Loss SNV dbSNP153 33..33 33 - - - 94547 RMVar_ID_94547 Human_SNP_ID_418339877 m1A Human chr9 + 137018045 137018045 137018045 AGCTGCCTGGCTCCACCACATCGTGCCCCACAAAAGTGTCGATGATGGCGCGCTCCATCATGTCT AGCTGCCTGGCTCCACCACATCGTGCCCCACAGAAGTGTCGATGATGGCGCGCTCCATCATGTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137017995..137018076 26863196 MeRIP-seq:(Medium) rs1285515284 Functional Loss SNV dbSNP153 33..33 33 - - - 94548 RMVar_ID_94548 Human_SNP_ID_418340197 m1A Human chr9 - 137018754 137018754 137018754 CGACGAGGAGAGCATTGTCAACTACACCCTCAACCAGGCCTACCAGGACAACGTCACTGTTTTTG CGACGAGGAGAGCATTGTCAACTACACCCTCAGCCAGGCCTACCAGGACAACGTCACTGTTTTTG T C ABCA2 Ensembl:ENSG00000107331 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137018671..137018755 26863196 MeRIP-seq:(Medium) rs1369421082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26833832 Human_Splice_Rec_1101572,Human_Splice_Rec_1101573,Human_Splice_Rec_1101664,Human_Splice_Rec_1101665,Human_Splice_Rec_1101758,Human_Splice_Rec_1101759,Human_Splice_Rec_1101850,Human_Splice_Rec_1101851,Human_Splice_Rec_1102012,Human_Splice_Rec_1102013,Human_Splice_Rec_1102104,Human_Splice_Rec_1102105,Human_Splice_Rec_1102280,Human_Splice_Rec_1102281,Human_Splice_Rec_1102290 RMVar_hsa_circ_101033,RMVar_hsa_circ_260961 94549 RMVar_ID_94549 Human_SNP_ID_418343564 m1A Human chr9 - 137028163 137028163 137028163 CGGGGCGCGCAGAGGAGCGGGCCGCGGCGCTGAGGCGGCGGAGCGTGGCCCCGCCATGGGCTTCC CGGGGCGCGCAGAGGAGCGGGCCGCGGCGCTGGGGCGGCGGAGCGTGGCCCCGCCATGGGCTTCC T C ABCA2 Ensembl:ENSG00000107331 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137028116..137028204 26863196 MeRIP-seq:(Medium) rs1281823701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5021424 Human_Splice_Rec_1101549,Human_Splice_Rec_1101645,Human_Splice_Rec_1101737,Human_Splice_Rec_1102261,Human_Splice_Rec_1102293,Human_Splice_Rec_1102307 94550 RMVar_ID_94550 Human_SNP_ID_418347523 m1A Human chr9 - 137039775 137039775 137039775 CTGCCGGCCCCCAGCTCACCGCCTGCACTGCCATGACCTGGAGGCAGACAGACGCCCACCTGCTC CTGCCGGCCCCCAGCTCACCGCCTGCACTGCCCTGACCTGGAGGCAGACAGACGCCCACCTGCTC T G AL807752.6,NPDC1 Ensembl:ENSG00000279073,Ensembl:ENSG00000107281 Protein coding,Protein coding intron,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:137039726..137039896 26863196 MeRIP-seq:(Medium) rs1251911270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5021448,Human_RBP_ID_8700400,Human_RBP_ID_26562553 Human_Splice_Rec_1102398,Human_Splice_Rec_1102412,Human_Splice_Rec_1102414,Human_Splice_Rec_1102418 94551 RMVar_ID_94551 Human_SNP_ID_418349007 m1A Human chr9 + 137043072 137043072 137043072 GCACAGTCCAGGCTCCCGGGACAGGCGGCTACATCTGGGAAGGAAGCAGAAGGCAGGGCCGGCTC GCACAGTCCAGGCTCCCGGGACAGGCGGCTACGTCTGGGAAGGAAGCAGAAGGCAGGGCCGGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137043026..137043140 26863410 MeRIP-seq:(Medium) rs771103148 Functional Loss SNV dbSNP153 33..33 33 - - - 94552 RMVar_ID_94552 Human_SNP_ID_418349437 m1A Human chr9 + 137044422 137044422 137044422 TGAGGCAGTCCCCGCTCCTGTGCTGATACCCCACCGTCCACCACGCCAAAGGCAGGGGCCTGAGG TGAGGCAGTCCCCGCTCCTGTGCTGATACCCCGCCGTCCACCACGCCAAAGGCAGGGGCCTGAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137044412..137044503 26863196 MeRIP-seq:(Medium) rs892128220 Functional Loss SNV dbSNP153 33..33 33 - - - 94553 RMVar_ID_94553 Human_SNP_ID_418351504 m1A Human chr9 - 137050096 137050090 137050096 TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTAAGGGCAGGCGGGTGGCTGGGAACTTTGTCGTGA TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTA______GGCGGGTGGCTGGGAACTTTGTCGTGA CTGCCCT C ENTPD2 Ensembl:ENSG00000054179 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137050026..137050200;chr9:137050038..137050156;chr9:137050017..137050319 26863196 MeRIP-seq:(Medium) rs1371780509 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_846398,Human_RBP_ID_3908421,Human_RBP_ID_8224384,Human_RBP_ID_8239490,Human_RBP_ID_9441884,Human_RBP_ID_18962602,Human_RBP_ID_19146588,Human_RBP_ID_21996179,Human_RBP_ID_22419590,Human_RBP_ID_22705034,Human_RBP_ID_26796884 94554 RMVar_ID_94554 Human_SNP_ID_418351510 m1A Human chr9 - 137050096 137050096 137050096 TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTAAGGGCAGGCGGGTGGCTGGGAACTTTGTCGTGA TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTAGGGGCAGGCGGGTGGCTGGGAACTTTGTCGTGA T C ENTPD2 Ensembl:ENSG00000054179 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137050026..137050200;chr9:137050038..137050156;chr9:137050017..137050319 26863196 MeRIP-seq:(Medium) rs12555382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_846398,Human_RBP_ID_3908421,Human_RBP_ID_8224384,Human_RBP_ID_8239490,Human_RBP_ID_9441884,Human_RBP_ID_18962602,Human_RBP_ID_19146588,Human_RBP_ID_21996179,Human_RBP_ID_22419590,Human_RBP_ID_22705034,Human_RBP_ID_26796884 94555 RMVar_ID_94555 Human_SNP_ID_418353009 m1A Human chr9 + 137053927 137053927 137053927 GCTCCCGGACGTCGCGGGTGGGGACGCACAGCAGTAGGAGGCCGGCGAGGCCCGCGGCGGCCAGC GCTCCCGGACGTCGCGGGTGGGGACGCACAGCGGTAGGAGGCCGGCGAGGCCCGCGGCGGCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137053924..137054015 26863196 MeRIP-seq:(Medium) rs1326872827 Functional Loss SNV dbSNP153 33..33 33 - - - 94556 RMVar_ID_94556 Human_SNP_ID_418356180 m1A Human chr9 - 137064670 137064670 137064670 TGAGCCAGCAGGACGGGGGACCTCTGGATTCCACCTTCATCTAGTCCTTGTGGGCCGCGTGGGCC TGAGCCAGCAGGACGGGGGACCTCTGGATTCCGCCTTCATCTAGTCCTTGTGGGCCGCGTGGGCC T C SAPCD2 Ensembl:ENSG00000186193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137064621..137064785 26863196 MeRIP-seq:(Medium) rs1344270128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5154598,Human_RBP_ID_8927497,Human_RBP_ID_9339333,Human_RBP_ID_18906217 94557 RMVar_ID_94557 Human_SNP_ID_418356813 m1A Human chr9 + 137066316 137066316 137066316 GCGATGGTGTGCCTCCGACGTTCCCCTCGGGCACGGGGAGCCCGCCGGGCATCCCCTGAGTCCGC GCGATGGTGTGCCTCCGACGTTCCCCTCGGGCTCGGGGAGCCCGCCGGGCATCCCCTGAGTCCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137066259..137066375 26863196 MeRIP-seq:(Medium) rs1270627712 Functional Loss SNV dbSNP153 33..33 33 - - - 94558 RMVar_ID_94558 Human_SNP_ID_418356828 m1A Human chr9 - 137066340 137066338 137066340 GCAGTGGCGTGCAGGGCCCTGGAGGCGGACTCAGGGGATGCCCGGCGGGCTCCCCGTGCCCGAGG GCAGTGGCGTGCAGGGCCCTGGAGGCGGACTC__GGGATGCCCGGCGGGCTCCCCGTGCCCGAGG CCT C SAPCD2 Ensembl:ENSG00000186193 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137066251..137066350 26863196 MeRIP-seq:(Medium) rs779849623 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_964298,Human_RBP_ID_5021695,Human_RBP_ID_18132582 Human_Splice_Rec_1102470,Human_Splice_Rec_1102471 94559 RMVar_ID_94559 Human_SNP_ID_418356830 m1A Human chr9 - 137066340 137066340 137066340 GCAGTGGCGTGCAGGGCCCTGGAGGCGGACTCAGGGGATGCCCGGCGGGCTCCCCGTGCCCGAGG GCAGTGGCGTGCAGGGCCCTGGAGGCGGACTCGGGGGATGCCCGGCGGGCTCCCCGTGCCCGAGG T C SAPCD2 Ensembl:ENSG00000186193 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137066251..137066350 26863196 MeRIP-seq:(Medium) rs750774599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964298,Human_RBP_ID_5021695,Human_RBP_ID_18132582 Human_Splice_Rec_1102470,Human_Splice_Rec_1102471 94560 RMVar_ID_94560 Human_SNP_ID_418358103 m1A Human chr9 - 137070438 137070438 137070438 CCGGGCGCCCATGGCCGGGGCCGCCATGGCCGAGCGGGGCCGCGTGCCTCCCCCCGCACCCGCGC CCGGGCGCCCATGGCCGGGGCCGCCATGGCCGCGCGGGGCCGCGTGCCTCCCCCCGCACCCGCGC T G SAPCD2 Ensembl:ENSG00000186193 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137070337..137070550 26863410 MeRIP-seq:(Medium) rs1205379728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036050,Human_RBP_ID_9339337,Human_RBP_ID_22466693 94561 RMVar_ID_94561 Human_SNP_ID_418360222 m1A Human chr9 - 137077651 137077648 137077651 GGCAGTGCTCGCGCAGCGCCTCGGGCTCCAGCAGCGCCAGCTCCGCCAGCAGCGCGGCTCGTGGC GGCAGTGCTCGCGCAGCGCCTCGGGCTCCAGC___GCCAGCTCCGCCAGCAGCGCGGCTCGTGGC CGCT C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137077551..137077676 26863410 MeRIP-seq:(Medium) rs1206573592 Functional Loss DEL dbSNP153 33..35 33 - - - 94562 RMVar_ID_94562 Human_SNP_ID_418362027 m1A Human chr9 + 137082695 137082695 137082695 GGAGTTCCAGTCCCCGCTCATCCTGGATGAAGACCAGGCCAGGGAGCCGCAGCTGCAGGAGTCCT GGAGTTCCAGTCCCCGCTCATCCTGGATGAAGTCCAGGCCAGGGAGCCGCAGCTGCAGGAGTCCT A T UAP1L1 Ensembl:ENSG00000197355 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137082644..137083243 32194978 MeRIP-seq:(Medium) rs780394935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847605,Human_RBP_ID_964301 Human_Splice_Rec_1102494,Human_Splice_Rec_1102510 RMVar_hsa_circ_79308,RMVar_hsa_circ_260969 94563 RMVar_ID_94563 Human_SNP_ID_418362156 m1A Human chr9 - 137083041 137083041 137083041 AACCCGAAGCCTCCTCTCAGCCCCATTCTCCCAGGTCCCAAGTCCCTCTGCCTCTTGACTAGACC AACCCGAAGCCTCCTCTCAGCCCCATTCTCCCTGGTCCCAAGTCCCTCTGCCTCTTGACTAGACC T A L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137082990..137083075 26863196 MeRIP-seq:(Medium) rs1045209423 Functional Loss SNV dbSNP153 33..33 33 - - - 94564 RMVar_ID_94564 Human_SNP_ID_418362315 m1A Human chr9 - 137083640 137083640 137083640 AATATGGAGGCTGCGTCCTCACTCGGAGAGCCAGGCAGCCTGAGCACCAAGATCCGTCAGAAGCA AATATGGAGGCTGCGTCCTCACTCGGAGAGCCCGGCAGCCTGAGCACCAAGATCCGTCAGAAGCA T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137083591..137083991 32194978 MeRIP-seq:(Medium) rs971776870 Functional Loss SNV dbSNP153 33..33 33 - - - 94565 RMVar_ID_94565 Human_SNP_ID_418363448 m1A Human chr9 + 137087024 137087024 137087024 GCGCTGCGATGGCTGCCTGCGAGGGCAGGAGAAGCGGAGCTCTCGGTTCCTCTCAGTCGGACTTC GCGCTGCGATGGCTGCCTGCGAGGGCAGGAGAGGCGGAGCTCTCGGTTCCTCTCAGTCGGACTTC A G MAN1B1 Ensembl:ENSG00000177239 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137086985..137087072 26863196 MeRIP-seq:(Medium) rs1047813903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036051,Human_RBP_ID_18427705 RMVar_hsa_circ_260971,RMVar_hsa_circ_103921 94566 RMVar_ID_94566 Human_SNP_ID_418366233 m1A Human chr9 + 137096298 137096298 137096298 ACCTCACCTGCAGATTAGACCCCCAAGCCAAGACCTGAAGGATGGGACCCAGGAGGAGGCCACAA ACCTCACCTGCAGATTAGACCCCCAAGCCAAGTCCTGAAGGATGGGACCCAGGAGGAGGCCACAA A T MAN1B1 Ensembl:ENSG00000177239 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137096200..137096323 26863196 MeRIP-seq:(Medium) rs886063728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3976235,Human_RBP_ID_22776605,Human_RBP_ID_24555503,Human_RBP_ID_26362402,Human_RBP_ID_27832938 Human_Splice_Rec_1102522,Human_Splice_Rec_1102523,Human_Splice_Rec_1102546,Human_Splice_Rec_1102547,Human_Splice_Rec_1102570,Human_Splice_Rec_1102571,Human_Splice_Rec_1102592,Human_Splice_Rec_1102600,Human_Splice_Rec_1102601,Human_Splice_Rec_1102614,Human_Splice_Rec_1102615,Human_Splice_Rec_1102624,Human_Splice_Rec_1102626,Human_Splice_Rec_1102627 Human_miRNA_ID_256063 Clinvar_Rec_540,Clinvar_Rec_5229 RMVar_hsa_circ_11340,RMVar_hsa_circ_87061,RMVar_hsa_circ_260971,RMVar_hsa_circ_103921,RMVar_hsa_circ_315366,RMVar_hsa_circ_296359,RMVar_hsa_circ_114338,RMVar_hsa_circ_51966,RMVar_hsa_circ_260972,RMVar_hsa_circ_342554,RMVar_hsa_circ_260973,RMVar_hsa_circ_118823,RMVar_hsa_circ_260974 94567 RMVar_ID_94567 Human_SNP_ID_418368316 m1A Human chr9 + 137102066 137102066 137102066 GGTTGGTGCTGTTACACACATGCTGTTGCAGGAGTACAGGTCGGTGGTGTTACATGCTGTTGCAG GGTTGGTGCTGTTACACACATGCTGTTGCAGGCGTACAGGTCGGTGGTGTTACATGCTGTTGCAG A C MAN1B1 Ensembl:ENSG00000177239 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137102057..137102168 26863196 MeRIP-seq:(Medium) rs1191350573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_846069,Human_RBP_ID_8159909,Human_RBP_ID_17174589,Human_RBP_ID_23300695 RMVar_hsa_circ_87061,RMVar_hsa_circ_260971,RMVar_hsa_circ_103921,RMVar_hsa_circ_114338,RMVar_hsa_circ_51966,RMVar_hsa_circ_260972,RMVar_hsa_circ_260973,RMVar_hsa_circ_118823,RMVar_hsa_circ_89598,RMVar_hsa_circ_84893,RMVar_hsa_circ_260974,RMVar_hsa_circ_90773,RMVar_hsa_circ_260976,RMVar_hsa_circ_260978,RMVar_hsa_circ_17075,RMVar_hsa_circ_260977 94568 RMVar_ID_94568 Human_SNP_ID_418371214 m1A Human chr9 + 137107376 137107376 137107376 AGACTTGTTACCAGATGAACCGGCAGATGGAGACGGGGCTGAGTCCCGAGATCGTGCACTTCAAC AGACTTGTTACCAGATGAACCGGCAGATGGAGGCGGGGCTGAGTCCCGAGATCGTGCACTTCAAC A G MAN1B1 Ensembl:ENSG00000177239 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137107325..137107478 26863196 MeRIP-seq:(Medium) rs1564313394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1102537,Human_Splice_Rec_1102561,Human_Splice_Rec_1102585,Human_Splice_Rec_1102641,Human_Splice_Rec_1102649,Human_Splice_Rec_1102659,Human_Splice_Rec_1102667,Human_Splice_Rec_1102673,Human_Splice_Rec_1102677,Human_Splice_Rec_1102679,Human_Splice_Rec_1102683 RMVar_hsa_circ_51966,RMVar_hsa_circ_90773,RMVar_hsa_circ_260978,RMVar_hsa_circ_17075,RMVar_hsa_circ_50916 94569 RMVar_ID_94569 Human_SNP_ID_418371462 m1A Human chr9 + 137107809 137107809 137107809 GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACACTGCAGCTTGGGGGCCCTGGCATCCCCATCCC GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACCCTGCAGCTTGGGGGCCCTGGCATCCCCATCCC A C MAN1B1 Ensembl:ENSG00000177239 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11790092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975234,Human_RBP_ID_5410649,Human_RBP_ID_9339339,Human_RBP_ID_18414476 RMVar_hsa_circ_90773,RMVar_hsa_circ_260978 94570 RMVar_ID_94570 Human_SNP_ID_418371463 m1A Human chr9 + 137107809 137107809 137107809 GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACACTGCAGCTTGGGGGCCCTGGCATCCCCATCCC GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACGCTGCAGCTTGGGGGCCCTGGCATCCCCATCCC A G MAN1B1 Ensembl:ENSG00000177239 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11790092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975234,Human_RBP_ID_5410649,Human_RBP_ID_9339339,Human_RBP_ID_18414476 RMVar_hsa_circ_90773,RMVar_hsa_circ_260978 94571 RMVar_ID_94571 Human_SNP_ID_418372071 m1A Human chr9 + 137109121 137109121 137109121 GGGGCTTGGAGGGCTGGACGGCAAGTCCGTCTAGCTCACGGGCCCCTCCAGTGGAATGGGTCTTT GGGGCTTGGAGGGCTGGACGGCAAGTCCGTCTTGCTCACGGGCCCCTCCAGTGGAATGGGTCTTT A T MAN1B1 Ensembl:ENSG00000177239 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:137109086..137109187 32194978 MeRIP-seq:(Medium) rs1366015124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715544,Human_RBP_ID_24293194 Human_miRNA_ID_2390234,Human_miRNA_ID_2591472 RMVar_hsa_circ_90773,RMVar_hsa_circ_260978 94572 RMVar_ID_94572 Human_SNP_ID_418372641 m1A Human chr9 - 137110645 137110645 137110645 CTGCGTGGGGGGCCCAGACTCAGCCTCTGAGCACAGGACTGGAGGGGTCTCAAGGCTCCTCATGG CTGCGTGGGGGGCCCAGACTCAGCCTCTGAGCGCAGGACTGGAGGGGTCTCAAGGCTCCTCATGG T C DPP7 Ensembl:ENSG00000176978 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137110596..137110719 26863196 MeRIP-seq:(Medium) rs777851739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91798,Human_RBP_ID_5154599 Human_miRNA_ID_1565083 RMVar_hsa_circ_81158,RMVar_hsa_circ_101654,RMVar_hsa_circ_122525,RMVar_hsa_circ_90241,RMVar_hsa_circ_260979,RMVar_hsa_circ_260981,RMVar_hsa_circ_260982,RMVar_hsa_circ_260980 94573 RMVar_ID_94573 Human_SNP_ID_418372709 m1A Human chr9 - 137110783 137110774 137110784 GCTGACGGGCCCCCTCTGTGCCCGCTCCCCAGAGCCTCCCACCCAGAAGATCCTGCTTCCGTGGT GCTGACGGGCCCCCTCTGTGCCCGCTCCCCA__________CCCAGAAGATCCTGCTTCCGTGGT GTGGGAGGCTC G DPP7 Ensembl:ENSG00000176978 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137110739..137112093 26863196 MeRIP-seq:(Medium) rs772716097 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_715547,Human_RBP_ID_18173115 Human_Splice_Rec_1102692,Human_Splice_Rec_1102710,Human_Splice_Rec_1102734,Human_Splice_Rec_1102744,Human_Splice_Rec_1102752 RMVar_hsa_circ_81158,RMVar_hsa_circ_101654,RMVar_hsa_circ_122525,RMVar_hsa_circ_90241,RMVar_hsa_circ_260979,RMVar_hsa_circ_260981,RMVar_hsa_circ_260982,RMVar_hsa_circ_260980 94574 RMVar_ID_94574 Human_SNP_ID_418372790 m1A Human chr9 - 137110895 137110895 137110895 AGTCATCGCCGTCACCATCCAGGGGGGAGCGCACCACCTCGACCTCAGGTGCGGAGGGAGGTGGC AGTCATCGCCGTCACCATCCAGGGGGGAGCGCGCCACCTCGACCTCAGGTGCGGAGGGAGGTGGC T C DPP7 Ensembl:ENSG00000176978 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137110575..137110973 26863196 MeRIP-seq:(Medium) rs760548777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5124293,Human_RBP_ID_18173116,Human_RBP_ID_18197072 Human_Splice_Rec_1102690,Human_Splice_Rec_1102691,Human_Splice_Rec_1102708,Human_Splice_Rec_1102709,Human_Splice_Rec_1102732,Human_Splice_Rec_1102733,Human_Splice_Rec_1102742,Human_Splice_Rec_1102743,Human_Splice_Rec_1102750,Human_Splice_Rec_1102751 RMVar_hsa_circ_81158,RMVar_hsa_circ_122525,RMVar_hsa_circ_90241,RMVar_hsa_circ_260979,RMVar_hsa_circ_260981,RMVar_hsa_circ_260980 94575 RMVar_ID_94575 Human_SNP_ID_418372823 m1A Human chr9 + 137110937 137110937 137110937 CCTGGATGGTGACGGCGATGACTGAGGCACTCAGGTTCCTCCGAATCTGTGGTCAGTGGAAAGAA CCTGGATGGTGACGGCGATGACTGAGGCACTCGGGTTCCTCCGAATCTGTGGTCAGTGGAAAGAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137110876..137110975 32194978 MeRIP-seq:(Medium) rs761585241 Functional Loss SNV dbSNP153 33..33 33 - - - 94576 RMVar_ID_94576 Human_SNP_ID_418373354 m1A Human chr9 + 137111977 137111977 137111977 GGCGGAGCTCGTCAGTGAAGGGCAGGTCCGGGAACATATCGGTCACATTGTTGCTGGCGAAGGTC GGCGGAGCTCGTCAGTGAAGGGCAGGTCCGGGGACATATCGGTCACATTGTTGCTGGCGAAGGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:137111874..137112269;chr9:137111926..137112257 26863196 MeRIP-seq:(Medium) rs761185569 Functional Loss SNV dbSNP153 33..33 33 - - - 94577 RMVar_ID_94577 Human_SNP_ID_418373802 m1A Human chr9 - 137112795 137112795 137112795 CGCCGCTGCCCCTGCACTCCAGGTGGGCTGTGATCGGCTGCTGAGTGAGGCCCAGAGGATCACGG CGCCGCTGCCCCTGCACTCCAGGTGGGCTGTGGTCGGCTGCTGAGTGAGGCCCAGAGGATCACGG T C DPP7 Ensembl:ENSG00000176978 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:137112707..137112816;chr9:137112700..137112805 26863196 MeRIP-seq:(Medium) rs372674817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3976247,Human_RBP_ID_16619453,Human_RBP_ID_26833836 Human_Splice_Rec_1102700,Human_Splice_Rec_1102701,Human_Splice_Rec_1102724,Human_Splice_Rec_1102725,Human_Splice_Rec_1102736,Human_Splice_Rec_1102764,Human_Splice_Rec_1102765,Human_Splice_Rec_1102778,Human_Splice_Rec_1102779,Human_Splice_Rec_1102784 RMVar_hsa_circ_90241,RMVar_hsa_circ_115463,RMVar_hsa_circ_260979,RMVar_hsa_circ_126416,RMVar_hsa_circ_260983,RMVar_hsa_circ_260984 94578 RMVar_ID_94578 Human_SNP_ID_418375010 m1A Human chr9 + 137114679 137114679 137114679 CCCCCGCCTGGAGGCCGCGCAGCCCGAGCGCCAGCAGCAGGACCGGGGCCCAGGGAGCGGAGCCC CCCCCGCCTGGAGGCCGCGCAGCCCGAGCGCCGGCAGCAGGACCGGGGCCCAGGGAGCGGAGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137114423..137114725 26863196 MeRIP-seq:(Medium) rs1428632166 Functional Loss SNV dbSNP153 33..33 33 - - - 94579 RMVar_ID_94579 Human_SNP_ID_418379747 m1A Human chr9 - 137129683 137129683 137129683 GCAATGGCTGCCCGCGAGTATCGGAGAGGCGGAGCTCTCAGTCTTTTACAGGACCGGGTCTCCTG GCAATGGCTGCCCGCGAGTATCGGAGAGGCGGGGCTCTCAGTCTTTTACAGGACCGGGTCTCCTG T C L13712-001,lnc-DPP7-2,lnc-DPP7-2:2,lnc-DPP7-2:3,lnc-DPP7-2:4 RNACentral:URS0000334622,RNACentral:URS00009B876F,RNACentral:URS0000D59C3A,RNACentral:URS00009B3CBC,RNACentral:URS00009BB481 misc_RNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137129432..137129722 26863196 MeRIP-seq:(Medium) rs1047023736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16619717 94580 RMVar_ID_94580 Human_SNP_ID_418388801 m1A Human chr9 - 137157076 137157076 137157076 CCCATCTCTGGAGTGACCCCGCCCACCTCCCCAAGAGCAGCCCCGCCCAGCTCCGGGGAGGCCCC CCCATCTCTGGAGTGACCCCGCCCACCTCCCCCAGAGCAGCCCCGCCCAGCTCCGGGGAGGCCCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137157072..137157240 26863196 MeRIP-seq:(Medium) rs1419138859 Functional Loss SNV dbSNP153 33..33 33 - - - 94581 RMVar_ID_94581 Human_SNP_ID_418389376 m1A Human chr9 - 137159193 137159193 137159193 AGTAGGGAGCCAAGGGAAAGATGTTCTGGAGGAGGAAGCCGGCGAGGGCAGAGGCTCTCAGAGGC AGTAGGGAGCCAAGGGAAAGATGTTCTGGAGGGGGAAGCCGGCGAGGGCAGAGGCTCTCAGAGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137159184..137159301 26863196 MeRIP-seq:(Medium) rs909749438 Functional Loss SNV dbSNP153 33..33 33 - - - 94582 RMVar_ID_94582 Human_SNP_ID_418390088 m1A Human chr9 + 137161444 137161444 137161444 AGCGGGTAGGCTGGACGGCGGGGGTGGGGACCAGCGTGAGAGGGGCCTGCAGGCGCGGTCGGAGT AGCGGGTAGGCTGGACGGCGGGGGTGGGGACCTGCGTGAGAGGGGCCTGCAGGCGCGGTCGGAGT A T GRIN1 Ensembl:ENSG00000176884 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137161442..137161513 26863196 MeRIP-seq:(Medium) rs533592868 Functional Loss SNV dbSNP153 33..33 33 - - - 94583 RMVar_ID_94583 Human_SNP_ID_418390808 m1A Human chr9 - 137163332 137163328 137163332 GGCGGAGGAGGGACGCGGGCGCACGGACACTCACTTGAGGATGGACAGGGAGACGTTCTGCTTCC GGCGGAGGAGGGACGCGGGCGCACGGACACTC____GAGGATGGACAGGGAGACGTTCTGCTTCC CAAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137163329..137163457 26863196 MeRIP-seq:(Medium) rs1048941579 Functional Loss DEL dbSNP153 33..36 33 - - - 94584 RMVar_ID_94584 Human_SNP_ID_418391314 m1A Human chr9 - 137164815 137164815 137164815 CTCAGGCCACACCAGCTGTCTGCGTGGAGGCCACTGACCCCCAAGGGGCACACACCAAGATTCAG CTCAGGCCACACCAGCTGTCTGCGTGGAGGCCGCTGACCCCCAAGGGGCACACACCAAGATTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137164812..137164878 26863196 MeRIP-seq:(Medium) rs774210322 Functional Loss SNV dbSNP153 33..33 33 - - - 94585 RMVar_ID_94585 Human_SNP_ID_418392071 m1A Human chr9 + 137167576 137167576 137167576 TCCTCTGCCCCCTCCCCCGCAGACAGACAGACAGACGGACGGGACAGCGGCCCGGCCCACGCAGA TCCTCTGCCCCCTCCCCCGCAGACAGACAGACGGACGGACGGGACAGCGGCCCGGCCCACGCAGA A G GRIN1 Ensembl:ENSG00000176884 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137167566..137167718 26863196 MeRIP-seq:(Medium) rs974552016 Functional Loss SNV dbSNP153 33..33 33 - - - 94586 RMVar_ID_94586 Human_SNP_ID_418392466 m1A Human chr9 + 137168838 137168838 137168838 GGCAAAGGCATGGGGGAAGCTTCGAGCGCTCCAGGCGGCCGCGGCCGCTCAGGCTTGGGCGGCAG GGCAAAGGCATGGGGGAAGCTTCGAGCGCTCCGGGCGGCCGCGGCCGCTCAGGCTTGGGCGGCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137168801..137169175 26863196 MeRIP-seq:(Medium) rs1235065467 Functional Loss SNV dbSNP153 33..33 33 - - - 94587 RMVar_ID_94587 Human_SNP_ID_418392525 m1A Human chr9 + 137168954 137168954 137168954 CGGGGTTCGGGTCTGGCGGTCTCGGCGGGCGGAGGGCGGCGGTGCGGAGGCGGCGGCGGCGCGCA CGGGGTTCGGGTCTGGCGGTCTCGGCGGGCGGGGGGCGGCGGTGCGGAGGCGGCGGCGGCGCGCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137168854..137169083 26863410 MeRIP-seq:(Medium) rs747146307 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 94588 RMVar_ID_94588 Human_SNP_ID_418392604 m1A Human chr9 - 137169077 137169077 137169077 TAGCCATTGCGCGCAGCCGCTCGCCCTGCGGGACCTGGCCGTGGTTTACACGCTCGGGCCGGCCT TAGCCATTGCGCGCAGCCGCTCGCCCTGCGGGTCCTGGCCGTGGTTTACACGCTCGGGCCGGCCT T A LRRC26,AL929554.2 Ensembl:ENSG00000184709,Ensembl:ENSG00000261793 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137168834..137169175 26863196 MeRIP-seq:(Medium) rs1198626729 Functional Loss SNV dbSNP153 33..33 33 - - - 94589 RMVar_ID_94589 Human_SNP_ID_418394793 m1A Human chr9 - 137174912 137174912 137174912 TGACACATCGCCCGCCCGCCCGCCCGCCCGCCAGGCGCTGCCCTGCAGGTGCTCTCGTCCTCCCG TGACACATCGCCCGCCCGCCCGCCCGCCCGCCCGGCGCTGCCCTGCAGGTGCTCTCGTCCTCCCG T G ANAPC2 Ensembl:ENSG00000176248 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137174833..137174938 26863410 MeRIP-seq:(Medium) rs1431490994 Functional Loss SNV dbSNP153 33..33 33 - - - 94590 RMVar_ID_94590 Human_SNP_ID_418395044 m1A Human chr9 + 137175406 137175406 137175406 CACGCAGCACACCCTGCTGCAGCCACACGGACATCCGCCGCCGCAGCAGCGCCACGGGCATCTTC CACGCAGCACACCCTGCTGCAGCCACACGGACGTCCGCCGCCGCAGCAGCGCCACGGGCATCTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137175365..137175516 32194978 MeRIP-seq:(Medium) rs371949799 Functional Loss SNV dbSNP153 33..33 33 - - - 94591 RMVar_ID_94591 Human_SNP_ID_418396331 m1A Human chr9 - 137179216 137179216 137179216 ACTGGGGGGAGGCGGGCACCCCAGCGGGGGACATGTGAGGAGAGGGTTCTGGGGCACAGCCAGCA ACTGGGGGGAGGCGGGCACCCCAGCGGGGGACGTGTGAGGAGAGGGTTCTGGGGCACAGCCAGCA T C ANAPC2 Ensembl:ENSG00000176248 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137179194..137179437 26863196 MeRIP-seq:(Medium) rs547743388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961912,Human_RBP_ID_3910766,Human_RBP_ID_5329820,Human_RBP_ID_8159921,Human_RBP_ID_8224388,Human_RBP_ID_9442560,Human_RBP_ID_16619847,Human_RBP_ID_17666439 RMVar_hsa_circ_103747,RMVar_hsa_circ_121009,RMVar_hsa_circ_260989,RMVar_hsa_circ_260990 94592 RMVar_ID_94592 Human_SNP_ID_418399794 m1A Human chr9 - 137188507 137188507 137188507 GGTGCAGATGGCGGCGGCAGTTGTGGTGGCGGAGGGGGACAGCGACTCCCGGCCCGGACAGGAGT GGTGCAGATGGCGGCGGCAGTTGTGGTGGCGGGGGGGGACAGCGACTCCCGGCCCGGACAGGAGT T C ANAPC2 Ensembl:ENSG00000176248 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:137188401..137188575;chr9:137187976..137188575 26863196 MeRIP-seq:(Medium) rs202152762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036605,Human_RBP_ID_5124123 Human_Splice_Rec_1103197,Human_Splice_Rec_1103241 94593 RMVar_ID_94593 Human_SNP_ID_418399997 m1A Human chr9 + 137188775 137188774 137188775 CGGCGCTGCAGAACTACAACAACGAGCTGGTCAAGTGTGAGCGGCGCAGCCGGGACGGGGAGGTC CGGCGCTGCAGAACTACAACAACGAGCTGGTC_AGTGTGAGCGGCGCAGCCGGGACGGGGAGGTC CA C SSNA1 Ensembl:ENSG00000176101 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137188676..137189150 26863410 MeRIP-seq:(Medium) rs1379629110 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_715578,Human_RBP_ID_5021998,Human_RBP_ID_18132618,Human_RBP_ID_27544717 Human_Splice_Rec_1103245,Human_Splice_Rec_1103251 94594 RMVar_ID_94594 Human_SNP_ID_418400163 m1A Human chr9 + 137189108 137189108 137189108 GCTGTGCCAGAAGCGGGAGGAGCTGTGCCGGCAGATCCAGGAGGAGGAGGACGAGAAGCAGCGGC GCTGTGCCAGAAGCGGGAGGAGCTGTGCCGGCCGATCCAGGAGGAGGAGGACGAGAAGCAGCGGC A C SSNA1 Ensembl:ENSG00000176101 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137188651..137190300 26863196 MeRIP-seq:(Medium) rs1351363841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715580,Human_RBP_ID_5036054,Human_RBP_ID_18140730,Human_RBP_ID_22467463,Human_RBP_ID_26362413,Human_RBP_ID_26566351 Human_Splice_Rec_1103246,Human_Splice_Rec_1103249,Human_Splice_Rec_1103252,Human_Splice_Rec_1103253 RMVar_hsa_circ_99499,RMVar_hsa_circ_260994 94595 RMVar_ID_94595 Human_SNP_ID_418400164 m1A Human chr9 + 137189108 137189108 137189108 GCTGTGCCAGAAGCGGGAGGAGCTGTGCCGGCAGATCCAGGAGGAGGAGGACGAGAAGCAGCGGC GCTGTGCCAGAAGCGGGAGGAGCTGTGCCGGCGGATCCAGGAGGAGGAGGACGAGAAGCAGCGGC A G SSNA1 Ensembl:ENSG00000176101 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137188651..137190300 26863196 MeRIP-seq:(Medium) rs1351363841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715580,Human_RBP_ID_5036054,Human_RBP_ID_18140730,Human_RBP_ID_22467463,Human_RBP_ID_26362413,Human_RBP_ID_26566351 Human_Splice_Rec_1103246,Human_Splice_Rec_1103249,Human_Splice_Rec_1103252,Human_Splice_Rec_1103253 RMVar_hsa_circ_99499,RMVar_hsa_circ_260994 94596 RMVar_ID_94596 Human_SNP_ID_418400180 m1A Human chr9 + 137189129 137189129 137189129 GCTGTGCCGGCAGATCCAGGAGGAGGAGGACGAGAAGCAGCGGCTGCAGAATGAGGTGAGGCAGC GCTGTGCCGGCAGATCCAGGAGGAGGAGGACGGGAAGCAGCGGCTGCAGAATGAGGTGAGGCAGC A G SSNA1 Ensembl:ENSG00000176101 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137188651..137189963 26863196 MeRIP-seq:(Medium) rs199697535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22467463,Human_RBP_ID_26362413,Human_RBP_ID_26566351 Human_Splice_Rec_1103246,Human_Splice_Rec_1103249,Human_Splice_Rec_1103252,Human_Splice_Rec_1103253 RMVar_hsa_circ_99499,RMVar_hsa_circ_260994 94597 RMVar_ID_94597 Human_SNP_ID_418400215 m1A Human chr9 + 137189204 137189204 137189204 GCTGGCCCGCGTCAACGAGAACCTGGCACGCAAGATTGCCTCTCGCAACGAGTTCGACCGGACCA GCTGGCCCGCGTCAACGAGAACCTGGCACGCAGGATTGCCTCTCGCAACGAGTTCGACCGGACCA A G SSNA1 Ensembl:ENSG00000176101 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137188951..137189275 32194978 MeRIP-seq:(Medium) rs898219178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26833838 Human_Splice_Rec_1103243,Human_Splice_Rec_1103247 RMVar_hsa_circ_99499,RMVar_hsa_circ_260994 94598 RMVar_ID_94598 Human_SNP_ID_418400564 m1A Human chr9 - 137190185 137190185 137190185 TGCTCAGACAACCAGAGCCTCCCTGGCAGGGCAGGAGTGTGGGTGCCACAGAGACAAGCCCCTTG TGCTCAGACAACCAGAGCCTCCCTGGCAGGGCGGGAGTGTGGGTGCCACAGAGACAAGCCCCTTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137190137..137190246 26863196 MeRIP-seq:(Medium) rs1460408968 Functional Loss SNV dbSNP153 33..33 33 - - - 94599 RMVar_ID_94599 Human_SNP_ID_418401320 m1A Human chr9 + 137192362 137192362 137192362 AGGCCACAGAGTGCTTCGGGGTGTAGCTGGACAGGCCTGTGAATGGAGGTGCACATGCAGACGTG AGGCCACAGAGTGCTTCGGGGTGTAGCTGGACTGGCCTGTGAATGGAGGTGCACATGCAGACGTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137192314..137192500 32194978 MeRIP-seq:(Medium) rs752691960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8700484 94600 RMVar_ID_94600 Human_SNP_ID_418401418 m1A Human chr9 + 137192544 137192544 137192544 GGGCAGGAAGAGTGCAAAGGGCTTCTCCTCTGAGCCGGATCCCTCTTCCTCCTCTTCCTCTTCCT GGGCAGGAAGAGTGCAAAGGGCTTCTCCTCTGGGCCGGATCCCTCTTCCTCCTCTTCCTCTTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137192493..137192610 26863196 MeRIP-seq:(Medium) rs1412647594 Functional Loss SNV dbSNP153 33..33 33 - - - 94601 RMVar_ID_94601 Human_SNP_ID_418401531 m1A Human chr9 + 137192701 137192701 137192701 TTGTCGTTGAAGGAGATCTTCATCTGGGAGTGAGAGTCACGTGAACGAGGGCTGAGGGCCCACAT TTGTCGTTGAAGGAGATCTTCATCTGGGAGTGGGAGTCACGTGAACGAGGGCTGAGGGCCCACAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137192699..137192799 32194978 MeRIP-seq:(Medium) rs1260950693 Functional Loss SNV dbSNP153 33..33 33 - - - 94602 RMVar_ID_94602 Human_SNP_ID_418402699 m1A Human chr9 - 137196887 137196887 137196887 GACGATACCTGGCATGGCCAGGTGGCCCGGGCAGGGCCCTGCCAGAGCAGCATGACCTGCTGGCT GACGATACCTGGCATGGCCAGGTGGCCCGGGCTGGGCCCTGCCAGAGCAGCATGACCTGCTGGCT T A TPRN Ensembl:ENSG00000176058 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137196879..137197066 26863196 MeRIP-seq:(Medium) rs1448050253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579161 RMVar_hsa_circ_260999,RMVar_hsa_circ_84228 94603 RMVar_ID_94603 Human_SNP_ID_418403419 m1A Human chr9 - 137199185 137199185 137199185 AACACCTTCACAGTGGTGCCCAAGAGGAAGCCAGGGACTCTGCAGGACCAGCACTTCAGTCAGGC AACACCTTCACAGTGGTGCCCAAGAGGAAGCCGGGGACTCTGCAGGACCAGCACTTCAGTCAGGC T C TPRN Ensembl:ENSG00000176058 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137199081..137199275 26863196 MeRIP-seq:(Medium) rs1327394650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5410662,Human_RBP_ID_7908239 Human_miRNA_ID_1514068,Human_miRNA_ID_2210359 RMVar_hsa_circ_100873,RMVar_hsa_circ_260999,RMVar_hsa_circ_84228,RMVar_hsa_circ_261000 94604 RMVar_ID_94604 Human_SNP_ID_418403473 m1A Human chr9 - 137199300 137199300 137199300 GGTAGACTCGGAGGAGGCCCCCCAAGCAGCCAAACTACCCTACCTCCCGCACCCTGCCAGGCCTC GGTAGACTCGGAGGAGGCCCCCCAAGCAGCCACACTACCCTACCTCCCGCACCCTGCCAGGCCTC T G TPRN Ensembl:ENSG00000176058 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137199249..137199363 26863196 MeRIP-seq:(Medium) rs1488099592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27544725 Human_miRNA_ID_1914196,Human_miRNA_ID_1916647,Human_miRNA_ID_1919096,Human_miRNA_ID_1921553,Human_miRNA_ID_1924010,Human_miRNA_ID_1926461,Human_miRNA_ID_1928913,Human_miRNA_ID_1931365,Human_miRNA_ID_2629195,Human_miRNA_ID_2642306,Human_miRNA_ID_3125046 RMVar_hsa_circ_100873,RMVar_hsa_circ_260999,RMVar_hsa_circ_84228,RMVar_hsa_circ_261000 94605 RMVar_ID_94605 Human_SNP_ID_418404125 m1A Human chr9 + 137200701 137200675 137200701 CCGCAGCGCGCGGCCCCGAGCCCGGCCGCCCCAGGGCGGCCATGCTGCGAACGCGGCAGCGGACG CCGCAGC__________________________GGGCGGCCATGCTGCGAACGCGGCAGCGGACG CGCGCGGCCCCGAGCCCGGCCGCCCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137199801..137200750 26863196 MeRIP-seq:(Medium) rs921735193 Functional Loss DEL dbSNP153 8..33 33 - - - 94606 RMVar_ID_94606 Human_SNP_ID_418404145 m1A Human chr9 + 137200701 137200701 137200701 CCGCAGCGCGCGGCCCCGAGCCCGGCCGCCCCAGGGCGGCCATGCTGCGAACGCGGCAGCGGACG CCGCAGCGCGCGGCCCCGAGCCCGGCCGCCCCGGGGCGGCCATGCTGCGAACGCGGCAGCGGACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137199801..137200750 26863196 MeRIP-seq:(Medium) rs1165184097 Functional Loss SNV dbSNP153 33..33 33 - - - 94607 RMVar_ID_94607 Human_SNP_ID_418405606 m1A Human chr9 - 137205484 137205484 137205484 CGCAGCAGCGGCGGCAGGCGCGGGCGAGGGCCACGGGGAGAGGAGACGCAGCCCCGCGGGTGGCA CGCAGCAGCGGCGGCAGGCGCGGGCGAGGGCCTCGGGGAGAGGAGACGCAGCCCCGCGGGTGGCA T A TMEM203 Ensembl:ENSG00000187713 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:137205467..137205598 26863196 MeRIP-seq:(Medium) rs1468275433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5022199 94608 RMVar_ID_94608 Human_SNP_ID_418405607 m1A Human chr9 - 137205484 137205484 137205484 CGCAGCAGCGGCGGCAGGCGCGGGCGAGGGCCACGGGGAGAGGAGACGCAGCCCCGCGGGTGGCA CGCAGCAGCGGCGGCAGGCGCGGGCGAGGGCCGCGGGGAGAGGAGACGCAGCCCCGCGGGTGGCA T C TMEM203 Ensembl:ENSG00000187713 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:137205467..137205598 26863196 MeRIP-seq:(Medium) rs1468275433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5022199 94609 RMVar_ID_94609 Human_SNP_ID_418405613 m1A Human chr9 - 137205510 137205510 137205510 GGCGGGGCCGCTCGCTGCCTCTCGCTCGCAGCAGCGGCGGCAGGCGCGGGCGAGGGCCACGGGGA GGCGGGGCCGCTCGCTGCCTCTCGCTCGCAGCGGCGGCGGCAGGCGCGGGCGAGGGCCACGGGGA T C TMEM203 Ensembl:ENSG00000187713 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:137205276..137205625 26863196 MeRIP-seq:(Medium) rs1268347627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715652,Human_RBP_ID_5022200,Human_RBP_ID_5244243,Human_RBP_ID_22119554,Human_RBP_ID_22466699 94610 RMVar_ID_94610 Human_SNP_ID_418405661 m1A Human chr9 - 137205626 137205626 137205626 GACGCGCCCTGTGGGGGCATGGCGTCCGATCGAGGCGGGCGTTCACGGGCGGCCAGGGTTGAGTC GACGCGCCCTGTGGGGGCATGGCGTCCGATCGGGGCGGGCGTTCACGGGCGGCCAGGGTTGAGTC T C TMEM203 Ensembl:ENSG00000187713 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs550823906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5022205 94611 RMVar_ID_94611 Human_SNP_ID_418405843 m1A Human chr9 - 137205887 137205887 137205887 CCCTCACCACCGGGTAGGAGTCCAGGGCCTGCACCCGGCAGCCAAGCCGCCGGCGCCGGGCCTCG CCCTCACCACCGGGTAGGAGTCCAGGGCCTGCTCCCGGCAGCCAAGCCGCCGGCGCCGGGCCTCG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137205726..137206009 26863196 MeRIP-seq:(Medium) rs200272893 Functional Loss SNV dbSNP153 33..33 33 - - - 94612 RMVar_ID_94612 Human_SNP_ID_418406303 m1A Human chr9 + 137207425 137207425 137207425 CACGGTGGGAGTAGGGGGCTGTGCAGGAAGGGAACCTGGAGACATTGAAGTGGAGAAGTGCAGTA CACGGTGGGAGTAGGGGGCTGTGCAGGAAGGGCACCTGGAGACATTGAAGTGGAGAAGTGCAGTA A C NDOR1 Ensembl:ENSG00000188566 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137207242..137207823 26863196 MeRIP-seq:(Medium) rs1564391926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797007,Human_RBP_ID_3195207 RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153 94613 RMVar_ID_94613 Human_SNP_ID_418408612 m1A Human chr9 + 137214341 137214340 137214342 GAAGCCCTTCCTAGCACCCATGATCTCCAACCAGAGAGTCACCGGCCCCTCCCACTTCCAGGACG GAAGCCCTTCCTAGCACCCATGATCTCCAACC__AGAGTCACCGGCCCCTCCCACTTCCAGGACG CAG C NDOR1 Ensembl:ENSG00000188566 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137214310..137214406 26863196 MeRIP-seq:(Medium) rs1413414357 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1103295,Human_Splice_Rec_1103323,Human_Splice_Rec_1103349 Human_miRNA_ID_2390236,Human_miRNA_ID_2591474 RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153,RMVar_hsa_circ_96901,RMVar_hsa_circ_264898,RMVar_hsa_circ_261003 94614 RMVar_ID_94614 Human_SNP_ID_418408613 m1A Human chr9 + 137214341 137214341 137214341 GAAGCCCTTCCTAGCACCCATGATCTCCAACCAGAGAGTCACCGGCCCCTCCCACTTCCAGGACG GAAGCCCTTCCTAGCACCCATGATCTCCAACCGGAGAGTCACCGGCCCCTCCCACTTCCAGGACG A G NDOR1 Ensembl:ENSG00000188566 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137214310..137214406 26863196 MeRIP-seq:(Medium) rs369326691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1103295,Human_Splice_Rec_1103323,Human_Splice_Rec_1103349 Human_miRNA_ID_2390236,Human_miRNA_ID_2591474 RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153,RMVar_hsa_circ_96901,RMVar_hsa_circ_264898,RMVar_hsa_circ_261003 94615 RMVar_ID_94615 Human_SNP_ID_418408791 m1A Human chr9 + 137214677 137214677 137214677 GGGCCTGGACCCTGACCAGCTCTTCATGCTGCAGCCGCGGGAGCCAGGTGAGCCCAGCCTCGGCC GGGCCTGGACCCTGACCAGCTCTTCATGCTGCGGCCGCGGGAGCCAGGTGAGCCCAGCCTCGGCC A G NDOR1 Ensembl:ENSG00000188566 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:137214626..137214700 32194978 MeRIP-seq:(Medium) rs770991148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19026315 Human_Splice_Rec_1103283,Human_Splice_Rec_1103297,Human_Splice_Rec_1103325,Human_Splice_Rec_1103351 Human_miRNA_ID_795976,Human_miRNA_ID_1937286,Human_miRNA_ID_1948386 RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153,RMVar_hsa_circ_96901,RMVar_hsa_circ_264898,RMVar_hsa_circ_261003,RMVar_hsa_circ_348016 94616 RMVar_ID_94616 Human_SNP_ID_418409138 m1A Human chr9 - 137215373 137215301 137215373 TGGGGAGGACGGCGGGGTGGGGGTGGTGGAACAAGGCTGCCCTCACCTGTGCCTGGGCCGTGGGC TGGGGAGGACGGCGGGGTGGGGGTGGTGGAAC_________________________________ CGTTCCCCCAGTCGGACTGCCTCTGCGGGAGGTAGGTGGGGCCCACGGCCCAGGCACAGGTGAGGGCAGCCTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137215353..137215475 26863196 MeRIP-seq:(Medium) rs1564400447 Functional Loss DEL dbSNP153 33..65 33 - - - 94617 RMVar_ID_94617 Human_SNP_ID_418410012 m1A Human chr9 + 137217376 137217365 137217376 AAGGCGGAACCAAGCCGTCCGTGCCGCTAGGGAGCCGAGACTGCCGGAAAGAGGAGCGGCAGGAG AAGGCGGAACCAAGCCGTCCGT___________GCCGAGACTGCCGGAAAGAGGAGCGGCAGGAG TGCCGCTAGGGA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137217326..137217443 26863196 MeRIP-seq:(Medium) rs1474467701 Functional Loss DEL dbSNP153 23..33 33 - - - RMVar_hsa_circ_264898 94618 RMVar_ID_94618 Human_SNP_ID_418410270 m1A Human chr9 + 137218067 137218065 137218068 GGGGAGAGAGCAGGCAGCAGGGCAGGGGGAAGAGGAGGAGTGCCCGATCTGCACAGAGCCCTACG GGGGAGAGAGCAGGCAGCAGGGCAGGGGGAA___GAGGAGTGCCCGATCTGCACAGAGCCCTACG AGAG A BX255925.3 Ensembl:ENSG00000284976 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137218017..137218082 26863196 MeRIP-seq:(Medium) rs1435267934 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_27134315 RMVar_hsa_circ_264898 94619 RMVar_ID_94619 Human_SNP_ID_418411767 m1A Human chr9 - 137222083 137222083 137222083 GCGGCCGCCGCCGGAGCCGCCGGAGCCCCCCGAGCTGCCGGGCCGAGGCGCGGGCGCCGCGTCCG GCGGCCGCCGCCGGAGCCGCCGGAGCCCCCCGCGCTGCCGGGCCGAGGCGCGGGCGCCGCGTCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137221879..137222194 26863196 MeRIP-seq:(Medium) rs1338674487 Functional Loss SNV dbSNP153 33..33 33 - - - 94620 RMVar_ID_94620 Human_SNP_ID_418412156 m1A Human chr9 + 137223267 137223266 137223268 AGAAGAGCAATAGGGAGAGGTGTGCGGGTGACAGGGGCGCTGCTGGAGGGGTCCTTACGGGGCCC AGAAGAGCAATAGGGAGAGGTGTGCGGGTGAC__GGGCGCTGCTGGAGGGGTCCTTACGGGGCCC CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137223156..137223352 26863196 MeRIP-seq:(Medium) rs896354126 Functional Loss DEL dbSNP153 33..34 33 - - - 94621 RMVar_ID_94621 Human_SNP_ID_418413148 m1A Human chr9 - 137225982 137225982 137225982 GGGGGGGCAGTGGCAGCAGTGGCAGCAGGGGCAGCAGCAGCAGTGGTGGGCGATGTCATCCCCGC GGGGGGGCAGTGGCAGCAGTGGCAGCAGGGGCTGCAGCAGCAGTGGTGGGCGATGTCATCCCCGC T A lnc-RNF208-1,lnc-RNF208-1:2,lnc-RNF208-1:3,lnc-RNF208-1:4,lnc-RNF208-1:5,lnc-RNF208-1:6 RNACentral:URS00008B8519,RNACentral:URS00008C0A0B,RNACentral:URS0000EA487D,RNACentral:URS00008C34B4,RNACentral:URS00009B8031,RNACentral:URS00009B0B59 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137225946..137226089 26863196 MeRIP-seq:(Medium) rs766034541 Functional Loss SNV dbSNP153 33..33 33 - - - 94622 RMVar_ID_94622 Human_SNP_ID_418413149 m1A Human chr9 - 137225982 137225982 137225982 GGGGGGGCAGTGGCAGCAGTGGCAGCAGGGGCAGCAGCAGCAGTGGTGGGCGATGTCATCCCCGC GGGGGGGCAGTGGCAGCAGTGGCAGCAGGGGCGGCAGCAGCAGTGGTGGGCGATGTCATCCCCGC T C lnc-RNF208-1,lnc-RNF208-1:2,lnc-RNF208-1:3,lnc-RNF208-1:4,lnc-RNF208-1:5,lnc-RNF208-1:6 RNACentral:URS00008B8519,RNACentral:URS00008C0A0B,RNACentral:URS0000EA487D,RNACentral:URS00008C34B4,RNACentral:URS00009B8031,RNACentral:URS00009B0B59 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137225946..137226089 26863196 MeRIP-seq:(Medium) rs766034541 Functional Loss SNV dbSNP153 33..33 33 - - - 94623 RMVar_ID_94623 Human_SNP_ID_418417039 m1A Human chr9 - 137234941 137234938 137234942 AGCTGAGAAAATGTGGAAGTGAGGAGGTCTCAAGGGAGGAGACGCAGGGAGGGTGTGAAATGTGT AGCTGAGAAAATGTGGAAGTGAGGAGGTCTC____GAGGAGACGCAGGGAGGGTGTGAAATGTGT CCCTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137234892..137235045 26863196 MeRIP-seq:(Medium) rs919626531 Functional Loss DEL dbSNP153 32..35 33 - - - 94624 RMVar_ID_94624 Human_SNP_ID_418417415 m1A Human chr9 - 137236000 137236000 137236000 CGGGATGGGCAGCCGCAGTGCAGGCACCAGGTACCACAGCAGGATGCCGGCCAGGTTGAAGAAGA CGGGATGGGCAGCCGCAGTGCAGGCACCAGGTGCCACAGCAGGATGCCGGCCAGGTTGAAGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137235990..137236137 26863196 MeRIP-seq:(Medium) rs1329546454 Functional Loss SNV dbSNP153 33..33 33 - - - 94625 RMVar_ID_94625 Human_SNP_ID_418419623 m1A Human chr9 + 137241405 137241405 137241405 GTGCACTTGCAGGCCGGGCAGTGCGGCAACCAAATCGGCGCCAAGGTAAGTTGCCGGGGCGCTGG GTGCACTTGCAGGCCGGGCAGTGCGGCAACCAGATCGGCGCCAAGGTAAGTTGCCGGGGCGCTGG A G TUBB4B Ensembl:ENSG00000188229 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:137241284..137241484 26863196 MeRIP-seq:(Medium) rs1004221423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798011,Human_RBP_ID_1058667,Human_RBP_ID_5036614,Human_RBP_ID_5124567,Human_RBP_ID_5431071,Human_RBP_ID_18132682,Human_RBP_ID_23216609,Human_RBP_ID_27843794 Human_Splice_Rec_1103469,Human_Splice_Rec_1103475 RMVar_hsa_circ_86963,RMVar_hsa_circ_261004 94626 RMVar_ID_94626 Human_SNP_ID_418420309 m1A Human chr9 + 137242513 137242513 137242513 TGTGTTCTCTCACAGGTCAGAGTGGTGCTGGGAACAACTGGGCCAAGGGGCACTACACAGAAGGC TGTGTTCTCTCACAGGTCAGAGTGGTGCTGGGGACAACTGGGCCAAGGGGCACTACACAGAAGGC A G TUBB4B Ensembl:ENSG00000188229 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11545615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287027,Human_RBP_ID_847172,Human_RBP_ID_1058671,Human_RBP_ID_3976258,Human_RBP_ID_5022421,Human_RBP_ID_8700540,Human_RBP_ID_17716261,Human_RBP_ID_18132686,Human_RBP_ID_19144519,Human_RBP_ID_22117529,Human_RBP_ID_22466702,Human_RBP_ID_22690683,Human_RBP_ID_22748393,Human_RBP_ID_24293315,Human_RBP_ID_27373749 Human_Splice_Rec_1103474 Human_miRNA_ID_2217769 RMVar_hsa_circ_80561,RMVar_hsa_circ_102310,RMVar_hsa_circ_86963,RMVar_hsa_circ_261004,RMVar_hsa_circ_117450,RMVar_hsa_circ_261005,RMVar_hsa_circ_261006,RMVar_hsa_circ_261007 94627 RMVar_ID_94627 Human_SNP_ID_418420323 m1A Human chr9 - 137242561 137242561 137242561 CTCAGCCTCCTTTCTCACAACATCCAGCACCGAGTCCACCAGCTCCGCGCCTTCTGTGTAGTGCC CTCAGCCTCCTTTCTCACAACATCCAGCACCGCGTCCACCAGCTCCGCGCCTTCTGTGTAGTGCC T G lnc-FAM166A-3 RNACentral:URS0000D5C5A6 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137242476..137242625 26863196 MeRIP-seq:(Medium) rs903103718 Functional Loss SNV dbSNP153 33..33 33 - - - 94628 RMVar_ID_94628 Human_SNP_ID_418420326 m1A Human chr9 - 137242565 137242565 137242565 AGCTCTCAGCCTCCTTTCTCACAACATCCAGCACCGAGTCCACCAGCTCCGCGCCTTCTGTGTAG AGCTCTCAGCCTCCTTTCTCACAACATCCAGCGCCGAGTCCACCAGCTCCGCGCCTTCTGTGTAG T C lnc-FAM166A-3 RNACentral:URS0000D5C5A6 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:137242476..137242725 26863196 MeRIP-seq:(Medium) rs893210425 Functional Loss SNV dbSNP153 33..33 33 - - - 94629 RMVar_ID_94629 Human_SNP_ID_418420331 m1A Human chr9 - 137242575 137242575 137242575 AGGCAGTCACAGCTCTCAGCCTCCTTTCTCACAACATCCAGCACCGAGTCCACCAGCTCCGCGCC AGGCAGTCACAGCTCTCAGCCTCCTTTCTCACGACATCCAGCACCGAGTCCACCAGCTCCGCGCC T C lnc-FAM166A-3 RNACentral:URS0000D5C5A6 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137242551..137242575 26863196 MeRIP-seq:(Medium) rs1197226915 Functional Loss SNV dbSNP153 33..33 33 - - - 94630 RMVar_ID_94630 Human_SNP_ID_418420668 m1A Human chr9 + 137243543 137243543 137243543 GGAGGAGGGCGAGTTCGAGGAGGAGGCTGAGGAGGAGGTGGCCTAGAGCCTTCAGTCACTGGGGA GGAGGAGGGCGAGTTCGAGGAGGAGGCTGAGGTGGAGGTGGCCTAGAGCCTTCAGTCACTGGGGA A T TUBB4B Ensembl:ENSG00000188229 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr9:137243426..137243657;chr9:137243426..137243649;chr9:137243426..137243600 26863196 MeRIP-seq:(Medium) rs1158708712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91870,Human_RBP_ID_715698,Human_RBP_ID_5022473,Human_RBP_ID_5124302,Human_RBP_ID_7908284,Human_RBP_ID_8239118,Human_RBP_ID_17666442,Human_RBP_ID_22466292,Human_RBP_ID_27373764 Human_miRNA_ID_2015914 RMVar_hsa_circ_80561,RMVar_hsa_circ_102310,RMVar_hsa_circ_86963,RMVar_hsa_circ_261004,RMVar_hsa_circ_117450,RMVar_hsa_circ_261005,RMVar_hsa_circ_261006,RMVar_hsa_circ_261007 94631 RMVar_ID_94631 Human_SNP_ID_418420688 m1A Human chr9 - 137243566 137243566 137243566 GAGTTCACACTGCTTCCCTGCTTTCCCCAGTGACTGAAGGCTCTAGGCCACCTCCTCCTCAGCCT GAGTTCACACTGCTTCCCTGCTTTCCCCAGTGCCTGAAGGCTCTAGGCCACCTCCTCCTCAGCCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:137243551..137243575 26863196 MeRIP-seq:(Medium) rs375069372 Functional Loss SNV dbSNP153 33..33 33 - - - 94632 RMVar_ID_94632 Human_SNP_ID_418425614 m1A Human chr9 + 137255346 137255346 137255346 GGCGGAAGTGGGCGGCTGCGGGACGCGCGCGGAGTCGCGCGGCGGGCGGGACCTGGCCGAGCTGG GGCGGAAGTGGGCGGCTGCGGGACGCGCGCGGGGTCGCGCGGCGGGCGGGACCTGGCCGAGCTGG A G NELFB Ensembl:ENSG00000188986 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137255246..137255917 26863196 MeRIP-seq:(Medium) rs1426765532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715704,Human_RBP_ID_798026,Human_RBP_ID_5036059,Human_RBP_ID_5409220,Human_RBP_ID_8731495,Human_RBP_ID_9339362,Human_RBP_ID_9355136,Human_RBP_ID_9442979,Human_RBP_ID_18427269,Human_RBP_ID_18962614,Human_RBP_ID_22534483,Human_RBP_ID_24555505 RMVar_hsa_circ_261009,RMVar_hsa_circ_105724,RMVar_hsa_circ_114440,RMVar_hsa_circ_123031,RMVar_hsa_circ_261010,RMVar_hsa_circ_261011 94633 RMVar_ID_94633 Human_SNP_ID_418425654 m1A Human chr9 - 137255439 137255439 137255439 CCCCAGCCCGTTCCCCCGGCGCCGCCGCAGACACCCCAGAAGCCCGCTCCGCCGGGCCTCGGGGA CCCCAGCCCGTTCCCCCGGCGCCGCCGCAGACGCCCCAGAAGCCCGCTCCGCCGGGCCTCGGGGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137255303..137255525 26863196 MeRIP-seq:(Medium) rs1398277040 Functional Loss SNV dbSNP153 33..33 33 - - - 94634 RMVar_ID_94634 Human_SNP_ID_418426224 m1A Human chr9 - 137256878 137256878 137256878 TTGCCAGATCTGCCGCTTCACCTCCACGGCGCAGGCTCGATACAGCTCCTTGTCAGCCATAACCA TTGCCAGATCTGCCGCTTCACCTCCACGGCGCGGGCTCGATACAGCTCCTTGTCAGCCATAACCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137256794..137257077 26863196 MeRIP-seq:(Medium) rs1259798839 Functional Loss SNV dbSNP153 33..33 33 - - - 94635 RMVar_ID_94635 Human_SNP_ID_418426249 m1A Human chr9 - 137256940 137256940 137256940 TTCTCCAGGATGTACTGCTTCAGGAGTGGGGAAACCTCGTCCCCGAAGAGGGCCTGGTTGTCTTG TTCTCCAGGATGTACTGCTTCAGGAGTGGGGACACCTCGTCCCCGAAGAGGGCCTGGTTGTCTTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137256890..137257006 26863196 MeRIP-seq:(Medium) rs751037466 Functional Loss SNV dbSNP153 33..33 33 - - - 94636 RMVar_ID_94636 Human_SNP_ID_418428442 m1A Human chr9 + 137262994 137262994 137262994 GTCGCCGGGCGTGACGTCCCTGTGTCTGGCGGAGCCCAGGACGGTCTGGGGGCCTGACAGTGCCT GTCGCCGGGCGTGACGTCCCTGTGTCTGGCGGGGCCCAGGACGGTCTGGGGGCCTGACAGTGCCT A G NELFB Ensembl:ENSG00000188986 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137262990..137263061 26863196 MeRIP-seq:(Medium) rs1386289213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22556504,Human_RBP_ID_22690978 RMVar_hsa_circ_93913,RMVar_hsa_circ_261009,RMVar_hsa_circ_105724,RMVar_hsa_circ_114440,RMVar_hsa_circ_123031,RMVar_hsa_circ_261010,RMVar_hsa_circ_261011,RMVar_hsa_circ_374613,RMVar_hsa_circ_97344,RMVar_hsa_circ_90638,RMVar_hsa_circ_261014,RMVar_hsa_circ_18736,RMVar_hsa_circ_79629,RMVar_hsa_circ_261015,RMVar_hsa_circ_261012,RMVar_hsa_circ_261013,RMVar_hsa_circ_107348,RMVar_hsa_circ_370260,RMVar_hsa_circ_261022,RMVar_hsa_circ_127899,RMVar_hsa_circ_261019,RMVar_hsa_circ_261020,RMVar_hsa_circ_261018,RMVar_hsa_circ_123893,RMVar_hsa_circ_261021 94637 RMVar_ID_94637 Human_SNP_ID_418429931 m1A Human chr9 - 137267052 137267052 137267052 AGTGAAGCTTTCGGGAAGTGTGTTTGGATATGAGACTGGGGCTTTCTCCTCAGCCGGAAGTTTCT AGTGAAGCTTTCGGGAAGTGTGTTTGGATATGGGACTGGGGCTTTCTCCTCAGCCGGAAGTTTCT T C HSALNG0075385 RNACentral:URS0000E99C05 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137267002..137267263 26863196 MeRIP-seq:(Medium) rs746566888 Functional Loss SNV dbSNP153 33..33 33 - - - 94638 RMVar_ID_94638 Human_SNP_ID_418429932 m1A Human chr9 - 137267052 137267052 137267052 AGTGAAGCTTTCGGGAAGTGTGTTTGGATATGAGACTGGGGCTTTCTCCTCAGCCGGAAGTTTCT AGTGAAGCTTTCGGGAAGTGTGTTTGGATATGCGACTGGGGCTTTCTCCTCAGCCGGAAGTTTCT T G HSALNG0075385 RNACentral:URS0000E99C05 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137267002..137267263 26863196 MeRIP-seq:(Medium) rs746566888 Functional Loss SNV dbSNP153 33..33 33 - - - 94639 RMVar_ID_94639 Human_SNP_ID_418430489 m1A Human chr9 + 137268808 137268808 137268808 ATGAGAGACAAAGATGAGAGACACAGAGACAGAGATGAGACACAGAGAGATGAGAGACAGGTAAG ATGAGAGACAAAGATGAGAGACACAGAGACAGCGATGAGACACAGAGAGATGAGAGACAGGTAAG A C NELFB Ensembl:ENSG00000188986 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137268664..137268967 26863196 MeRIP-seq:(Medium) rs1357215460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16620452,Human_RBP_ID_23316622 RMVar_hsa_circ_123031,RMVar_hsa_circ_261011,RMVar_hsa_circ_374613,RMVar_hsa_circ_79629,RMVar_hsa_circ_261012,RMVar_hsa_circ_261013,RMVar_hsa_circ_107348,RMVar_hsa_circ_261022,RMVar_hsa_circ_127899,RMVar_hsa_circ_261020,RMVar_hsa_circ_92784,RMVar_hsa_circ_261024,RMVar_hsa_circ_122484,RMVar_hsa_circ_36544,RMVar_hsa_circ_261026,RMVar_hsa_circ_91902,RMVar_hsa_circ_261027,RMVar_hsa_circ_122067,RMVar_hsa_circ_261028 94640 RMVar_ID_94640 Human_SNP_ID_418431845 m1A Human chr9 + 137272928 137272928 137272928 CTCCCCAGCGTGCCCGCCCCTGCCCCGCTCTGAGGGCCCTCCAGACCTGCTCGGGTGCTGGGGCC CTCCCCAGCGTGCCCGCCCCTGCCCCGCTCTGCGGGCCCTCCAGACCTGCTCGGGTGCTGGGGCC A C NELFB Ensembl:ENSG00000188986 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137272776..137273221 26863196 MeRIP-seq:(Medium) rs1239853474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715726 Human_miRNA_ID_2792705 RMVar_hsa_circ_123031,RMVar_hsa_circ_261011,RMVar_hsa_circ_107348,RMVar_hsa_circ_261022,RMVar_hsa_circ_127899,RMVar_hsa_circ_261020,RMVar_hsa_circ_92784,RMVar_hsa_circ_261024,RMVar_hsa_circ_91902,RMVar_hsa_circ_261027,RMVar_hsa_circ_122067,RMVar_hsa_circ_261028,RMVar_hsa_circ_261030,RMVar_hsa_circ_103545 94641 RMVar_ID_94641 Human_SNP_ID_418433777 m1A Human chr9 - 137278943 137278943 137278943 GCCGGCGCTTCTTGCGTGGCGTCCTGGAGGGTAGCTCCGCGGGGCTGTCGAAGGTGAAGAACTTT GCCGGCGCTTCTTGCGTGGCGTCCTGGAGGGTGGCTCCGCGGGGCTGTCGAAGGTGAAGAACTTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137278816..137278942 26863196 MeRIP-seq:(Medium) rs1319336346 Functional Loss SNV dbSNP153 33..33 33 - - - 94642 RMVar_ID_94642 Human_SNP_ID_418434298 m1A Human chr9 + 137279971 137279971 137279971 TGGCCACGGTGAACCTCCTGTAGTGGAGGCGCAGGACGGGACGTTTGGGTTGATGGCGGCAGTAG TGGCCACGGTGAACCTCCTGTAGTGGAGGCGCTGGACGGGACGTTTGGGTTGATGGCGGCAGTAG A T TOR4A Ensembl:ENSG00000198113 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137279871..137279995 26863196 MeRIP-seq:(Medium) rs754297841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5330351 RMVar_hsa_circ_113849,RMVar_hsa_circ_261031 94643 RMVar_ID_94643 Human_SNP_ID_418434355 m1A Human chr9 + 137280207 137280190 137280207 CCAAACTTGCCCATTGCCCTGCTGGGCGTCCCAGGCATGGTCTGGTGCGTTCTCCCTGTGGCCCC CCAAACTTGCCCATTG_________________GGCATGGTCTGGTGCGTTCTCCCTGTGGCCCC GCCCTGCTGGGCGTCCCA G TOR4A Ensembl:ENSG00000198113 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137279892..137280742 32194978 MeRIP-seq:(Medium) rs1371302047 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_5037326,Human_RBP_ID_5155127,Human_RBP_ID_22372571,Human_RBP_ID_26565657 Human_miRNA_ID_1699191 RMVar_hsa_circ_113849,RMVar_hsa_circ_261031 94644 RMVar_ID_94644 Human_SNP_ID_418434364 m1A Human chr9 + 137280207 137280207 137280207 CCAAACTTGCCCATTGCCCTGCTGGGCGTCCCAGGCATGGTCTGGTGCGTTCTCCCTGTGGCCCC CCAAACTTGCCCATTGCCCTGCTGGGCGTCCCGGGCATGGTCTGGTGCGTTCTCCCTGTGGCCCC A G TOR4A Ensembl:ENSG00000198113 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137279892..137280742 32194978 MeRIP-seq:(Medium) rs1260563118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037326,Human_RBP_ID_5155127,Human_RBP_ID_22372571,Human_RBP_ID_26565657 Human_miRNA_ID_1699191 RMVar_hsa_circ_113849,RMVar_hsa_circ_261031 94645 RMVar_ID_94645 Human_SNP_ID_418438935 m1A Human chr9 - 137295640 137295640 137295640 GCCCCGGCCCGGTCCGCGGGGGCATGCGAGGCAGGGGAGGGGGCGCGCCCGGGGCTCCCACCGAC GCCCCGGCCCGGTCCGCGGGGGCATGCGAGGCGGGGGAGGGGGCGCGCCCGGGGCTCCCACCGAC T C BX255925.1 Ensembl:ENSG00000260996 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr9:137295601..137295650 26863196 MeRIP-seq:(Medium) rs1235038512 Functional Loss SNV dbSNP153 33..33 33 - - - 94646 RMVar_ID_94646 Human_SNP_ID_418440375 m1A Human chr9 + 137300729 137300729 137300729 TGGTGGCCTCATCCAGGAGGGGCGGGGGAGAGAGGCCCTGGGGCTTCCAAAACTCACGGATTTGA TGGTGGCCTCATCCAGGAGGGGCGGGGGAGAGCGGCCCTGGGGCTTCCAAAACTCACGGATTTGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137300626..137300857 26863196 MeRIP-seq:(Medium) rs1279480368 Functional Loss SNV dbSNP153 33..33 33 - - - 94647 RMVar_ID_94647 Human_SNP_ID_418440558 m1A Human chr9 - 137301372 137301372 137301372 TGCGGCCTAGCCGGGCCCGGCCGGGCCGGAGCAGCTTCCCACGGCCCCCACCCGCTCGCCTGCCC TGCGGCCTAGCCGGGCCCGGCCGGGCCGGAGCGGCTTCCCACGGCCCCCACCCGCTCGCCTGCCC T C NRARP Ensembl:ENSG00000198435 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137301362..137301595 26863196 MeRIP-seq:(Medium) rs555899039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18197078,Human_RBP_ID_22119204 Human_miRNA_ID_634993 94648 RMVar_ID_94648 Human_SNP_ID_418440822 m1A Human chr9 - 137302159 137302159 137302159 GCCGCCGTCCCCGGCCGGGCCCGGCCCCCGCGAGCCGAGCGCGCGCCCCCGTCGCCCACCCGGGC GCCGCCGTCCCCGGCCGGGCCCGGCCCCCGCGTGCCGAGCGCGCGCCCCCGTCGCCCACCCGGGC T A NRARP Ensembl:ENSG00000198435 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr9:137301955..137302275;chr9:137301906..137302250 26863410 MeRIP-seq:(Medium) rs1463038741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256923,Human_RBP_ID_962921,Human_RBP_ID_5022742 94649 RMVar_ID_94649 Human_SNP_ID_418440838 m1A Human chr9 - 137302211 137302187 137302211 GGGACCGCGTGGGAGCCGCAGCCGAACCGAGTAGGGACCGGGACCGCGCGGCGCCGCCGTCCCCG GGGACCGCGTGGGAGCCGCAGCCGAACCGAGT________________________CCGTCCCCG GCGGCGCCGCGCGGTCCCGGTCCCT G NRARP Ensembl:ENSG00000198435 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr9:137302111..137302275;chr9:137302109..137302246 26863196,26863410 MeRIP-seq:(Medium) rs1376471221 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_5036620 94650 RMVar_ID_94650 Human_SNP_ID_418442447 m1A Human chr9 - 137307071 137307071 137307071 GCGGTGCTTCTACTGCTGCACGGGCTGTGGAAAGGTCTTCTGGGACGGCTCCCACCTGGGTCGTG GCGGTGCTTCTACTGCTGCACGGGCTGTGGAAGGGTCTTCTGGGACGGCTCCCACCTGGGTCGTG T C EXD3 Ensembl:ENSG00000187609 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137307035..137307150 32194978 MeRIP-seq:(Medium) rs1382613538 Functional Loss SNV dbSNP153 33..33 33 - - - 94651 RMVar_ID_94651 Human_SNP_ID_418449829 m1A Human chr9 + 137328756 137328756 137328756 ACACGGGACTACACGGGGCTACACGGGACTACACGGGACTACACGGGGCTACACGGGACTACACG ACACGGGACTACACGGGGCTACACGGGACTACGCGGGACTACACGGGGCTACACGGGACTACACG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137328656..137329063 26863196 MeRIP-seq:(Medium) rs1481412478 Functional Loss SNV dbSNP153 33..33 33 - - - 94652 RMVar_ID_94652 Human_SNP_ID_418450560 m1A Human chr9 + 137329716 137329656 137329716 GGGTCACACGGGACTACACGGGACTACACGGGACTACACGGGACTACACGGGGTCACACGGGACT _________________________________CTACACGGGACTACACGGGGTCACACGGGACT GCTACACGGGACTACACGGGACTACACGGGGTCACACGGGACTACACGGGACTACACGGGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137329313..137329809 26863196 MeRIP-seq:(Medium) rs1564479932 Functional Loss DEL dbSNP153 1..33 33 - - - 94653 RMVar_ID_94653 Human_SNP_ID_418450605 m1A Human chr9 + 137329716 137329716 137329716 GGGTCACACGGGACTACACGGGACTACACGGGACTACACGGGACTACACGGGGTCACACGGGACT GGGTCACACGGGACTACACGGGACTACACGGGGCTACACGGGACTACACGGGGTCACACGGGACT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137329313..137329809 26863196 MeRIP-seq:(Medium) rs111207789 Functional Loss SNV dbSNP153 33..33 33 - - - 94654 RMVar_ID_94654 Human_SNP_ID_418458834 m1A Human chr9 - 137354725 137354725 137354725 GGCCATTCAGCAGCGCCTGGCGGCCCTGCGGCACCTGTGCCACAAGCGGTTTGTGGAGGTTCGTG GGCCATTCAGCAGCGCCTGGCGGCCCTGCGGCTCCTGTGCCACAAGCGGTTTGTGGAGGTTCGTG T A EXD3 Ensembl:ENSG00000187609 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137354674..137354774 32194978 MeRIP-seq:(Medium) rs1257440042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1103602,Human_Splice_Rec_1103642,Human_Splice_Rec_1103643,Human_Splice_Rec_1103734,Human_Splice_Rec_1103752,Human_Splice_Rec_1103753 RMVar_hsa_circ_43214,RMVar_hsa_circ_61714,RMVar_hsa_circ_35336 94655 RMVar_ID_94655 Human_SNP_ID_418466437 m1A Human chr9 - 137378856 137378856 137378856 CGTCACCCACAAACCCTGTACCCCTCACACAGACGCCCCATTCCCCTTGTCACACAGGCCCTAGC CGTCACCCACAAACCCTGTACCCCTCACACAGTCGCCCCATTCCCCTTGTCACACAGGCCCTAGC T A EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137378842..137379001 26863196 MeRIP-seq:(Medium) rs1334165531 Functional Loss SNV dbSNP153 33..33 33 - - - 94656 RMVar_ID_94656 Human_SNP_ID_418466821 m1A Human chr9 - 137379816 137379816 137379816 AAGGTTTACGGGACTGAAGCAGGAGTGAGGGAAGGCGGGCTGTGGTTAGAACGGGTGCTGCAGAA AAGGTTTACGGGACTGAAGCAGGAGTGAGGGAGGGCGGGCTGTGGTTAGAACGGGTGCTGCAGAA T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137379809..137379960 26863196 MeRIP-seq:(Medium) rs1410023494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906725,Human_RBP_ID_5135432,Human_RBP_ID_8160728,Human_RBP_ID_8224407,Human_RBP_ID_8944677,Human_RBP_ID_9442981,Human_RBP_ID_22733334 94657 RMVar_ID_94657 Human_SNP_ID_418467526 m1A Human chr9 - 137381601 137381601 137381601 GTGTTCCTCTAACGTGAGAGAGGAGCCAGCACACCGGGCGGGTGAGAGCAGCCTGGGAGACGGGC GTGTTCCTCTAACGTGAGAGAGGAGCCAGCACGCCGGGCGGGTGAGAGCAGCCTGGGAGACGGGC T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137381585..137381670 26863196 MeRIP-seq:(Medium) rs1249195123 Functional Loss SNV dbSNP153 33..33 33 - - - 94658 RMVar_ID_94658 Human_SNP_ID_418467673 m1A Human chr9 + 137382004 137382001 137382004 TGGGAGCACGCAGAGGAGGTGAGGACGCGGGGAGGAGGTGAGGACGCGGGGAGGAGGTGAGGGCG TGGGAGCACGCAGAGGAGGTGAGGACGCGG___GGAGGTGAGGACGCGGGGAGGAGGTGAGGGCG GGGA G RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr9:137382001..137382050 26863196 MeRIP-seq:(Medium) rs1490337919 Functional Loss DEL dbSNP153 31..33 33 - - - 94659 RMVar_ID_94659 Human_SNP_ID_418467733 m1A Human chr9 - 137382067 137382067 137382067 CACCGCCGCCCTGACCTCCACCGCGCGCCCTCACCTCCTCCGCGCGCCCTCACCTCCTCCCCGCG CACCGCCGCCCTGACCTCCACCGCGCGCCCTCCCCTCCTCCGCGCGCCCTCACCTCCTCCCCGCG T G EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:137381963..137382353;chr9:137382001..137382134 26863196 MeRIP-seq:(Medium) rs1489466175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3908452,Human_RBP_ID_21996196,Human_RBP_ID_22484744 94660 RMVar_ID_94660 Human_SNP_ID_418469262 m1A Human chr9 - 137386840 137386840 137386840 GGGGGCCAGGCAGGGAGCAGGGGTGCTGAGGGAGGCAGGCAGGGAGCAGGTGTGCTGAGGGGGCC GGGGGCCAGGCAGGGAGCAGGGGTGCTGAGGGGGGCAGGCAGGGAGCAGGTGTGCTGAGGGGGCC T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137386534..137387300 26863196 MeRIP-seq:(Medium) rs1218469259 Functional Loss SNV dbSNP153 33..33 33 - - - 94661 RMVar_ID_94661 Human_SNP_ID_418469328 m1A Human chr9 - 137387035 137387035 137387035 AGCACGGAGCAGGGGTGCTGAGGGAGGCAGGCAGGGAGCAGGGGTGCTGAGGGGGCCAGGCAGGG AGCACGGAGCAGGGGTGCTGAGGGAGGCAGGCGGGGAGCAGGGGTGCTGAGGGGGCCAGGCAGGG T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:137386934..137387078 26863196 MeRIP-seq:(Medium) rs1564198377 Functional Loss SNV dbSNP153 33..33 33 - - - 94662 RMVar_ID_94662 Human_SNP_ID_418471408 m1A Human chr9 + 137393122 137393122 137393122 GGGGTGCCGTGTCTGTTCCAGGGAGGGCCATTAGTGTTCCAGGGGGCGCCGAGGCTGTTCCAGGG GGGGTGCCGTGTCTGTTCCAGGGAGGGCCATTGGTGTTCCAGGGGGCGCCGAGGCTGTTCCAGGG A G RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137393114..137393246 26863196 MeRIP-seq:(Medium) rs1472851948 Functional Loss SNV dbSNP153 33..33 33 - - - 94663 RMVar_ID_94663 Human_SNP_ID_418471838 m1A Human chr9 - 137394558 137394558 137394558 GTTAGGGAAGCGGAGGCTGGAAGGCCGGGATTAGGGAAGCGGAGGCTGGGAGGCCGGGGTTAGGG GTTAGGGAAGCGGAGGCTGGAAGGCCGGGATTGGGGAAGCGGAGGCTGGGAGGCCGGGGTTAGGG T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137394386..137394663 26863196 MeRIP-seq:(Medium) rs1318210685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22628999 94664 RMVar_ID_94664 Human_SNP_ID_418475691 m1A Human chr9 - 137407158 137407158 137407158 GGCGCTGCCGGGTTCCACCAGCAGAGGGGCCCAGAGACCGGCCCGGACGCGCGGCGGTCGGCGTG GGCGCTGCCGGGTTCCACCAGCAGAGGGGCCCGGAGACCGGCCCGGACGCGCGGCGGTCGGCGTG T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137407149..137407338 26863196 MeRIP-seq:(Medium) rs1229456118 Functional Loss SNV dbSNP153 33..33 33 - - - 94665 RMVar_ID_94665 Human_SNP_ID_418478494 m1A Human chr9 + 137416395 137416395 137416395 TCTGCCACCTTCCCATCAGGCCGGGCACCCCCAGGTCCAGCTCACACTCCACCGCAGCTTCTGCA TCTGCCACCTTCCCATCAGGCCGGGCACCCCCCGGTCCAGCTCACACTCCACCGCAGCTTCTGCA A C RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137416385..137416592 26863196 MeRIP-seq:(Medium) rs966159953 Functional Loss SNV dbSNP153 33..33 33 - - - 94666 RMVar_ID_94666 Human_SNP_ID_418478495 m1A Human chr9 + 137416395 137416395 137416395 TCTGCCACCTTCCCATCAGGCCGGGCACCCCCAGGTCCAGCTCACACTCCACCGCAGCTTCTGCA TCTGCCACCTTCCCATCAGGCCGGGCACCCCCGGGTCCAGCTCACACTCCACCGCAGCTTCTGCA A G RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137416385..137416592 26863196 MeRIP-seq:(Medium) rs966159953 Functional Loss SNV dbSNP153 33..33 33 - - - 94667 RMVar_ID_94667 Human_SNP_ID_418480716 m1A Human chr9 + 137423441 137423441 137423441 GCGCTTGGCGCCCGCACCTCTGCCCGCCTCGGAGACCCCGCAGCCCCGCGCCGCCGCCTGGCCCC GCGCTTGGCGCCCGCACCTCTGCCCGCCTCGGTGACCCCGCAGCCCCGCGCCGCCGCCTGGCCCC A T NOXA1 Ensembl:ENSG00000188747 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137423414..137423650 26863196 MeRIP-seq:(Medium) rs1041246842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5228194,Human_RBP_ID_9339381,Human_RBP_ID_26796907 94668 RMVar_ID_94668 Human_SNP_ID_418483416 m1A Human chr9 - 137431477 137431477 137431477 ATCCTCCCATCTGGCTGGGCTGGGCCAGGACCACGGGTGAGCCCGGCCCCGTCTACCCCCCAGCG ATCCTCCCATCTGGCTGGGCTGGGCCAGGACCGCGGGTGAGCCCGGCCCCGTCTACCCCCCAGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137431458..137431595 26863196 MeRIP-seq:(Medium) rs1349144184 Functional Loss SNV dbSNP153 33..33 33 - - - 94669 RMVar_ID_94669 Human_SNP_ID_418484506 m1A Human chr9 + 137434353 137434353 137434353 CGGCCGCCTGCCCCGATCCCAGCAGGGAGATCAGCCCTAATGATGCTGTGTCCATGATGCTTTTA CGGCCGCCTGCCCCGATCCCAGCAGGGAGATCGGCCCTAATGATGCTGTGTCCATGATGCTTTTA A G NOXA1 Ensembl:ENSG00000188747 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137434208..137434357 32194978 MeRIP-seq:(Medium) rs978781668 Functional Loss SNV dbSNP153 33..33 33 - - - 94670 RMVar_ID_94670 Human_SNP_ID_418489219 m1A Human chr9 + 137448319 137448319 137448319 CCCCGCCCCAGCCCTCCCTCAGCTGGGAACACAGCCAGGTGCCCTCAGACCCCTGGCTCTGCACA CCCCGCCCCAGCCCTCCCTCAGCTGGGAACACGGCCAGGTGCCCTCAGACCCCTGGCTCTGCACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137448271..137448343 26863196 MeRIP-seq:(Medium) rs1424214552 Functional Loss SNV dbSNP153 33..33 33 - - - 94671 RMVar_ID_94671 Human_SNP_ID_418489585 m1A Human chr9 - 137449370 137449370 137449370 GTCCTGTGAGGGGCAGAGGCCTCCGCCCAGTCACCATCAGGCCACTCCCTCTGCACCGGGACCTG GTCCTGTGAGGGGCAGAGGCCTCCGCCCAGTCGCCATCAGGCCACTCCCTCTGCACCGGGACCTG T C NSMF Ensembl:ENSG00000165802 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137449322..137449402 26863196 MeRIP-seq:(Medium) rs1376222630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5154610,Human_RBP_ID_23091227,Human_RBP_ID_27373880 94672 RMVar_ID_94672 Human_SNP_ID_418489835 m1A Human chr9 - 137449914 137449914 137449914 CTGGGGAACCCCAATGGAGAGAAGGTACAGTGACCCCCAAGCCCCACCCCAGACCTCTGGAAACC CTGGGGAACCCCAATGGAGAGAAGGTACAGTGGCCCCCAAGCCCCACCCCAGACCTCTGGAAACC T C NSMF Ensembl:ENSG00000165802 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137449913..137449996 26863196 MeRIP-seq:(Medium) rs1039642165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52047,RMVar_hsa_circ_107783,RMVar_hsa_circ_13084,RMVar_hsa_circ_32797,RMVar_hsa_circ_261033 94673 RMVar_ID_94673 Human_SNP_ID_418491859 m1A Human chr9 - 137454477 137454477 137454477 GCTAGGTGGGCAGGGGCTGCCGTCACCCTCTCACGGCCCTCTTCAGCCCCTGGCTTCCTCCCCCA GCTAGGTGGGCAGGGGCTGCCGTCACCCTCTCGCGGCCCTCTTCAGCCCCTGGCTTCCTCCCCCA T C NSMF Ensembl:ENSG00000165802 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137454468..137454733 26863196 MeRIP-seq:(Medium) rs866337822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964330,Human_RBP_ID_3975267,Human_RBP_ID_5407642,Human_RBP_ID_19147959,Human_RBP_ID_22556520,Human_RBP_ID_22690697,Human_RBP_ID_26212061 Human_Splice_Rec_1103923,Human_Splice_Rec_1103951,Human_Splice_Rec_1103977,Human_Splice_Rec_1104007,Human_Splice_Rec_1104025,Human_Splice_Rec_1104049,Human_Splice_Rec_1104077,Human_Splice_Rec_1104095,Human_Splice_Rec_1104119 RMVar_hsa_circ_28216,RMVar_hsa_circ_52047,RMVar_hsa_circ_95519,RMVar_hsa_circ_261035,RMVar_hsa_circ_261037,RMVar_hsa_circ_117134,RMVar_hsa_circ_373633,RMVar_hsa_circ_261036 94674 RMVar_ID_94674 Human_SNP_ID_418491860 m1A Human chr9 - 137454477 137454477 137454477 GCTAGGTGGGCAGGGGCTGCCGTCACCCTCTCACGGCCCTCTTCAGCCCCTGGCTTCCTCCCCCA GCTAGGTGGGCAGGGGCTGCCGTCACCCTCTCCCGGCCCTCTTCAGCCCCTGGCTTCCTCCCCCA T G NSMF Ensembl:ENSG00000165802 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137454468..137454733 26863196 MeRIP-seq:(Medium) rs866337822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964330,Human_RBP_ID_3975267,Human_RBP_ID_5407642,Human_RBP_ID_19147959,Human_RBP_ID_22556520,Human_RBP_ID_22690697,Human_RBP_ID_26212061 Human_Splice_Rec_1103923,Human_Splice_Rec_1103951,Human_Splice_Rec_1103977,Human_Splice_Rec_1104007,Human_Splice_Rec_1104025,Human_Splice_Rec_1104049,Human_Splice_Rec_1104077,Human_Splice_Rec_1104095,Human_Splice_Rec_1104119 RMVar_hsa_circ_28216,RMVar_hsa_circ_52047,RMVar_hsa_circ_95519,RMVar_hsa_circ_261035,RMVar_hsa_circ_261037,RMVar_hsa_circ_117134,RMVar_hsa_circ_373633,RMVar_hsa_circ_261036 94675 RMVar_ID_94675 Human_SNP_ID_418491883 m1A Human chr9 - 137454515 137454515 137454515 CACCGAAGGGGTGAGAGTAGAGCCATGACCCGACGGGGGCTAGGTGGGCAGGGGCTGCCGTCACC CACCGAAGGGGTGAGAGTAGAGCCATGACCCGGCGGGGGCTAGGTGGGCAGGGGCTGCCGTCACC T C NSMF Ensembl:ENSG00000165802 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:137454508..137454701;chr9:137454503..137454643 26863196 MeRIP-seq:(Medium) rs1176755710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975267,Human_RBP_ID_5407642,Human_RBP_ID_22556520 RMVar_hsa_circ_28216,RMVar_hsa_circ_52047,RMVar_hsa_circ_95519,RMVar_hsa_circ_261035,RMVar_hsa_circ_261037,RMVar_hsa_circ_117134,RMVar_hsa_circ_373633,RMVar_hsa_circ_261036 94676 RMVar_ID_94676 Human_SNP_ID_418493333 m1A Human chr9 - 137458546 137458546 137458546 CTCTGACCGTGCCCTCTGTCCACCCTCAGAGCAGCCCGAGCGTTTGGAGAGTACCTGTCCCAGAG CTCTGACCGTGCCCTCTGTCCACCCTCAGAGCTGCCCGAGCGTTTGGAGAGTACCTGTCCCAGAG T A NSMF Ensembl:ENSG00000165802 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137458476..137458550 26863196 MeRIP-seq:(Medium) rs1240433915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15990,Human_RBP_ID_5036076,Human_RBP_ID_19026370,Human_RBP_ID_22119766 Human_Splice_Rec_1103912,Human_Splice_Rec_1103913,Human_Splice_Rec_1103942,Human_Splice_Rec_1103943,Human_Splice_Rec_1103970,Human_Splice_Rec_1103971,Human_Splice_Rec_1103996,Human_Splice_Rec_1103997,Human_Splice_Rec_1104040,Human_Splice_Rec_1104041,Human_Splice_Rec_1104068,Human_Splice_Rec_1104069 RMVar_hsa_circ_261037,RMVar_hsa_circ_117134 94677 RMVar_ID_94677 Human_SNP_ID_418493515 m1A Human chr9 - 137459038 137459038 137459038 GAGGAGCGAGGCCATGTCCTCGGTGGCGGCCAAAGTGCGGTGAGTGCGGCGGGGCCGCCTTCCCG GAGGAGCGAGGCCATGTCCTCGGTGGCGGCCAGAGTGCGGTGAGTGCGGCGGGGCCGCCTTCCCG T C NSMF Ensembl:ENSG00000165802 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137459035..137459288 26863196 MeRIP-seq:(Medium) rs1449233725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715885,Human_RBP_ID_797884,Human_RBP_ID_5036077 Human_Splice_Rec_1103911,Human_Splice_Rec_1103941,Human_Splice_Rec_1103969,Human_Splice_Rec_1103995,Human_Splice_Rec_1104039,Human_Splice_Rec_1104067 RMVar_hsa_circ_261037,RMVar_hsa_circ_117134 94678 RMVar_ID_94678 Human_SNP_ID_418493529 m1A Human chr9 - 137459081 137459081 137459081 CCGCCTCGACCATGGGCGCCGCCGCCTCCAGGAGGAGGGCGCTGAGGAGCGAGGCCATGTCCTCG CCGCCTCGACCATGGGCGCCGCCGCCTCCAGGCGGAGGGCGCTGAGGAGCGAGGCCATGTCCTCG T G NSMF Ensembl:ENSG00000165802 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137459005..137459350 26863196 MeRIP-seq:(Medium) rs915747302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036078,Human_RBP_ID_22629010 Human_Splice_Rec_1103911,Human_Splice_Rec_1103941,Human_Splice_Rec_1103969,Human_Splice_Rec_1103995,Human_Splice_Rec_1104039,Human_Splice_Rec_1104067 RMVar_hsa_circ_261037,RMVar_hsa_circ_117134 94679 RMVar_ID_94679 Human_SNP_ID_418496374 m1A Human chr9 + 137466870 137466870 137466870 CCATCACCTCAGACCCGGGCACGGATCAGACCACCTCCCACCACCGTCTCCACCAACTCAGACCC CCATCACCTCAGACCCGGGCACGGATCAGACCGCCTCCCACCACCGTCTCCACCAACTCAGACCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137466853..137467068 26863196 MeRIP-seq:(Medium) rs376839240 Functional Loss SNV dbSNP153 33..33 33 - - - 94680 RMVar_ID_94680 Human_SNP_ID_418501377 m1A Human chr9 + 137485046 137485046 137485046 GAGGCTACCTGGGCCTCACGCTGTCCCCAGCCATGTGGCTGCCTAGGCCTCACGCCTTCTCCAGG GAGGCTACCTGGGCCTCACGCTGTCCCCAGCCGTGTGGCTGCCTAGGCCTCACGCCTTCTCCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137485035..137485150 26863196 MeRIP-seq:(Medium) rs1310768140 Functional Loss SNV dbSNP153 33..33 33 - - - 94681 RMVar_ID_94681 Human_SNP_ID_418504000 m1A Human chr9 - 137494681 137494681 137494681 GTGAAGGCACAGAGTGGATGAGGTCATGGAGCAGGTGAGGGCAGGGCACAGGTGAGGGCGCGGAG GTGAAGGCACAGAGTGGATGAGGTCATGGAGCGGGTGAGGGCAGGGCACAGGTGAGGGCGCGGAG T C PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137494612..137494951 26863196 MeRIP-seq:(Medium) rs1405653421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68505,RMVar_hsa_circ_55214 94682 RMVar_ID_94682 Human_SNP_ID_418504008 m1A Human chr9 - 137494705 137494705 137494705 GGAGCTGGTGAGGGCGCAGAGCAGGTGAAGGCACAGAGTGGATGAGGTCATGGAGCAGGTGAGGG GGAGCTGGTGAGGGCGCAGAGCAGGTGAAGGCGCAGAGTGGATGAGGTCATGGAGCAGGTGAGGG T C PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137494654..137494772 26863196 MeRIP-seq:(Medium) rs1362111244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68505,RMVar_hsa_circ_55214 94683 RMVar_ID_94683 Human_SNP_ID_418504050 m1A Human chr9 - 137494807 137494791 137494808 AGAGTGGATGAGGTCACGGAGCAGGTGAGGGCAGGGCGCAGGTGAGGGTGCGGAGTGGATGAGGT AGAGTGGATGAGGTCACGGAGCAGGTGAGGG_________________TGCGGAGTGGATGAGGT ACCCTCACCTGCGCCCTG A PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137494801..137494943 26863196 MeRIP-seq:(Medium) rs1289346200 Functional Loss DEL dbSNP153 32..48 33 - - - RMVar_hsa_circ_68505,RMVar_hsa_circ_55214 94684 RMVar_ID_94684 Human_SNP_ID_418504099 m1A Human chr9 - 137494907 137494907 137494907 AGCAGGTGAGGGCGCGGAGCAGGTGAGAGCGCAGAGCAGGTGAAGGCGCGGAGTGGATGAGGTCA AGCAGGTGAGGGCGCGGAGCAGGTGAGAGCGCGGAGCAGGTGAAGGCGCGGAGTGGATGAGGTCA T C PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137494856..137494934 26863196 MeRIP-seq:(Medium) rs1421714345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68505,RMVar_hsa_circ_55214 94685 RMVar_ID_94685 Human_SNP_ID_418512215 m1A Human chr9 + 137517010 137517006 137517010 TCACTCACTCAACTCTGTCCACTCCATCCCCCACTCACTCCACTCTGTCCACTCCATCCCCTGTC TCACTCACTCAACTCTGTCCACTCCATCC____CTCACTCCACTCTGTCCACTCCATCCCCTGTC CCCCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137516942..137517141 26863196 MeRIP-seq:(Medium) rs1291465631 Functional Loss DEL dbSNP153 30..33 33 - - - 94686 RMVar_ID_94686 Human_SNP_ID_418512330 m1A Human chr9 - 137517273 137517241 137517273 GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGAGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT GGATGGAGTGGACAGAGTGGAGTGAGTGAGTG________________________________T ACTCACTCACTCCACTCTGTCCACTCCATCCCT A PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137517222..137517410;chr9:137516961..137517572 26863196 MeRIP-seq:(Medium) rs1171593435 Functional Loss DEL dbSNP153 33..64 33 - - - Human_RBP_ID_24293485 RMVar_hsa_circ_55214 94687 RMVar_ID_94687 Human_SNP_ID_418512340 m1A Human chr9 - 137517273 137517273 137517273 GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGAGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGTGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT T A PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137517222..137517410;chr9:137516961..137517572 26863196 MeRIP-seq:(Medium) rs377731762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24293485 RMVar_hsa_circ_55214 94688 RMVar_ID_94688 Human_SNP_ID_418512341 m1A Human chr9 - 137517273 137517273 137517273 GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGAGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGGGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT T C PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137517222..137517410;chr9:137516961..137517572 26863196 MeRIP-seq:(Medium) rs377731762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24293485 RMVar_hsa_circ_55214 94689 RMVar_ID_94689 Human_SNP_ID_418512342 m1A Human chr9 - 137517273 137517273 137517273 GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGAGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGCGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT T G PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137517222..137517410;chr9:137516961..137517572 26863196 MeRIP-seq:(Medium) rs377731762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24293485 RMVar_hsa_circ_55214 94690 RMVar_ID_94690 Human_SNP_ID_418512351 m1A Human chr9 + 137517307 137517307 137517307 ACTCACTCACTCCACTCTGTCCACTCCATCCCACACTCACTCACTCCACTCTGTCCACTCCATCC ACTCACTCACTCCACTCTGTCCACTCCATCCCCCACTCACTCACTCCACTCTGTCCACTCCATCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137517264..137517348 26863196 MeRIP-seq:(Medium) rs1370605853 Functional Loss SNV dbSNP153 33..33 33 - - - 94691 RMVar_ID_94691 Human_SNP_ID_418512352 m1A Human chr9 + 137517307 137517307 137517307 ACTCACTCACTCCACTCTGTCCACTCCATCCCACACTCACTCACTCCACTCTGTCCACTCCATCC ACTCACTCACTCCACTCTGTCCACTCCATCCCTCACTCACTCACTCCACTCTGTCCACTCCATCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137517264..137517348 26863196 MeRIP-seq:(Medium) rs1370605853 Functional Loss SNV dbSNP153 33..33 33 - - - 94692 RMVar_ID_94692 Human_SNP_ID_418512699 m1A Human chr9 - 137518277 137518277 137518277 CAGAGTGGAGTCAGTGAGTGGGGGATGGAGTGAGCAGAGTGGAGTGAGTGAATGAGGGATGGAGT CAGAGTGGAGTCAGTGAGTGGGGGATGGAGTGGGCAGAGTGGAGTGAGTGAATGAGGGATGGAGT T C PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137517668..137518735 26863196 MeRIP-seq:(Medium) rs1163768808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5229584,Human_RBP_ID_24293502 RMVar_hsa_circ_55214 94693 RMVar_ID_94693 Human_SNP_ID_418512975 m1A Human chr9 + 137518881 137518881 137518881 CCCCCACTCACTCACTTCACTCTACTCACTCCATCCTCACTCACTCACTCCACTCTGCTCACTCC CCCCCACTCACTCACTTCACTCTACTCACTCCGTCCTCACTCACTCACTCCACTCTGCTCACTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137518793..137519168 26863196 MeRIP-seq:(Medium) rs1237167799 Functional Loss SNV dbSNP153 33..33 33 - - - 94694 RMVar_ID_94694 Human_SNP_ID_418513280 m1A Human chr9 + 137519662 137519662 137519662 CCTGGGGGGCCATCTGATGAGACCTGGGGGGCATGTGAGGTGACCTGGGGCACGTGTGAGGGGAC CCTGGGGGGCCATCTGATGAGACCTGGGGGGCGTGTGAGGTGACCTGGGGCACGTGTGAGGGGAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137519611..137519695 26863196 MeRIP-seq:(Medium) rs1454312531 Functional Loss SNV dbSNP153 33..33 33 - - - 94695 RMVar_ID_94695 Human_SNP_ID_418523088 m1A Human chr9 - 137551951 137551951 137551951 CTCACCTGGACCGGAGACCCCACACGAGCTCCAAGCGGCCCCGGCTCCGGCGCCAACCCGGCCTC CTCACCTGGACCGGAGACCCCACACGAGCTCCTAGCGGCCCCGGCTCCGGCGCCAACCCGGCCTC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr9:137551901..137552200;chr9:137551901..137552275;chr9:137551901..137552175;chr9:137551901..137552147 26863196 MeRIP-seq:(Medium) rs1165656637 Functional Loss SNV dbSNP153 33..33 33 - - - 94696 RMVar_ID_94696 Human_SNP_ID_418523252 m1A Human chr9 - 137552318 137552316 137552318 TGCGCGGCCGTCAGGGGCGTCTCCTCGCTCTCAGGGGCGAGGTAGCTCACGTAGGGCTTGAGCTT TGCGCGGCCGTCAGGGGCGTCTCCTCGCTCTC__GGGCGAGGTAGCTCACGTAGGGCTTGAGCTT CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137551829..137552507 32194978 MeRIP-seq:(Medium) rs1256000675 Functional Loss DEL dbSNP153 33..34 33 - - - 94697 RMVar_ID_94697 Human_SNP_ID_418527879 m1A Human chr9 - 137569052 137569052 137569052 CTTTTCTTGGAAGATTGGTTGTGGTTCAGTGCACCAACTCCTCTCTTCTCCCATCCTTTTCGTTC CTTTTCTTGGAAGATTGGTTGTGGTTCAGTGCCCCAACTCCTCTCTTCTCCCATCCTTTTCGTTC T G DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137569048..137569262 26863196 MeRIP-seq:(Medium) rs1045933637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906764,Human_RBP_ID_8159960,Human_RBP_ID_8224889,Human_RBP_ID_26212116 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94698 RMVar_ID_94698 Human_SNP_ID_418527895 m1A Human chr9 + 137569112 137569112 137569112 AAAAGCAATGCAGACATGGGGTGAATGGTGGCACCTGAAGGAAGGGAAGCTCAAGAGCAGGGCCC AAAAGCAATGCAGACATGGGGTGAATGGTGGCTCCTGAAGGAAGGGAAGCTCAAGAGCAGGGCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137569108..137569261 26863196 MeRIP-seq:(Medium) rs999009106 Functional Loss SNV dbSNP153 33..33 33 - - - 94699 RMVar_ID_94699 Human_SNP_ID_418528059 m1A Human chr9 - 137569592 137569588 137569592 TGGTGGGTGAGTGGCTGGCTGGCTGGCTTGATAGACGGGGGGTGGATGGATGGATTTTTGGGTGG TGGTGGGTGAGTGGCTGGCTGGCTGGCTTGAT____GGGGGGTGGATGGATGGATTTTTGGGTGG CGTCT C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137569586..137569857 26863196 MeRIP-seq:(Medium) rs1233118584 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3906769,Human_RBP_ID_5658800,Human_RBP_ID_8160761,Human_RBP_ID_8224449,Human_RBP_ID_8239029,Human_RBP_ID_8944765,Human_RBP_ID_9442594,Human_RBP_ID_17323177,Human_RBP_ID_24293579 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94700 RMVar_ID_94700 Human_SNP_ID_418528063 m1A Human chr9 - 137569592 137569592 137569592 TGGTGGGTGAGTGGCTGGCTGGCTGGCTTGATAGACGGGGGGTGGATGGATGGATTTTTGGGTGG TGGTGGGTGAGTGGCTGGCTGGCTGGCTTGATGGACGGGGGGTGGATGGATGGATTTTTGGGTGG T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137569586..137569857 26863196 MeRIP-seq:(Medium) rs1339280078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906769,Human_RBP_ID_5658800,Human_RBP_ID_8160761,Human_RBP_ID_8224449,Human_RBP_ID_8239029,Human_RBP_ID_8944765,Human_RBP_ID_9442594,Human_RBP_ID_17323177,Human_RBP_ID_24293579 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94701 RMVar_ID_94701 Human_SNP_ID_418528136 m1A Human chr9 - 137569785 137569785 137569785 GATGGTGGTGGTGGTGGCGTGGATAGATGGTGAGTGACTGGATAGATGGATGGTGGATTGTTGGA GATGGTGGTGGTGGTGGCGTGGATAGATGGTGGGTGACTGGATAGATGGATGGTGGATTGTTGGA T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137569763..137569864 26863196 MeRIP-seq:(Medium) rs1411302579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906771,Human_RBP_ID_5658803,Human_RBP_ID_8160763,Human_RBP_ID_8224451,Human_RBP_ID_8239030,Human_RBP_ID_24293584 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94702 RMVar_ID_94702 Human_SNP_ID_418528319 m1A Human chr9 - 137570398 137570398 137570398 GTTGGGTTCTGGATAGAAGTGAAGGTATATCCAGTCAGATTTCCTGATGGAGTGGATATGTGGGG GTTGGGTTCTGGATAGAAGTGAAGGTATATCCGGTCAGATTTCCTGATGGAGTGGATATGTGGGG T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137570395..137570507 26863196 MeRIP-seq:(Medium) rs1052232849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906775,Human_RBP_ID_5309439,Human_RBP_ID_7908537,Human_RBP_ID_8159966,Human_RBP_ID_8224895,Human_RBP_ID_8944681,Human_RBP_ID_9442228,Human_RBP_ID_21997029,Human_RBP_ID_24293594 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94703 RMVar_ID_94703 Human_SNP_ID_418528320 m1A Human chr9 - 137570398 137570398 137570398 GTTGGGTTCTGGATAGAAGTGAAGGTATATCCAGTCAGATTTCCTGATGGAGTGGATATGTGGGG GTTGGGTTCTGGATAGAAGTGAAGGTATATCCCGTCAGATTTCCTGATGGAGTGGATATGTGGGG T G DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137570395..137570507 26863196 MeRIP-seq:(Medium) rs1052232849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906775,Human_RBP_ID_5309439,Human_RBP_ID_7908537,Human_RBP_ID_8159966,Human_RBP_ID_8224895,Human_RBP_ID_8944681,Human_RBP_ID_9442228,Human_RBP_ID_21997029,Human_RBP_ID_24293594 RMVar_hsa_circ_9205,RMVar_hsa_circ_331421 94704 RMVar_ID_94704 Human_SNP_ID_418532031 m1A Human chr9 + 137582472 137582472 137582472 CGCAGCTGGCTTTTTTGGCACCTCCAGGTTCAACCACCAGTCTGTCTCTGCTGTGCCCAGGGTAG CGCAGCTGGCTTTTTTGGCACCTCCAGGTTCAGCCACCAGTCTGTCTCTGCTGTGCCCAGGGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137582421..137582637 26863196 MeRIP-seq:(Medium) rs1255623461 Functional Loss SNV dbSNP153 33..33 33 - - - 94705 RMVar_ID_94705 Human_SNP_ID_418532252 m1A Human chr9 + 137583101 137583101 137583101 CATTATAATACCGGGTCACATTTAGGACAGGAAACTGTTCTTCTATAGGGTCTGTAGGCAGCTGC CATTATAATACCGGGTCACATTTAGGACAGGACACTGTTCTTCTATAGGGTCTGTAGGCAGCTGC A C NONHSAG053875.2 RNACentral:URS00008BD8C3 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:137583051..137583100 32194978 MeRIP-seq:(Medium) rs1278543212 Functional Loss SNV dbSNP153 33..33 33 - - - 94706 RMVar_ID_94706 Human_SNP_ID_418533303 m1A Human chr9 - 137586552 137586545 137586553 CTCTGCTCACCTCAGGATTCCTTCCTTCTCTCACCTCAGGATTCCTTCCTTCTCTCACCTCAGGA CTCTGCTCACCTCAGGATTCCTTCCTTCTCT________GATTCCTTCCTTCTCTCACCTCAGGA CCTGAGGTG C ZMYND19 Ensembl:ENSG00000165724 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:137586291..137586600 26863196 MeRIP-seq:(Medium) rs1349360781 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_309546 94707 RMVar_ID_94707 Human_SNP_ID_418534681 m1A Human chr9 + 137590363 137590358 137590364 GGCCGCGGCGCGCCGGGACAGGACGGGACCGGAGCCGGGGTCGGGGTAGCAGCCAGGCGGGCTCC GGCCGCGGCGCGCCGGGACAGGACGGGA______CCGGGGTCGGGGTAGCAGCCAGGCGGGCTCC ACCGGAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137590182..137590500;chr9:137590201..137590450 26863196 MeRIP-seq:(Medium) rs1457322834 Functional Loss DEL dbSNP153 29..34 33 - - - 94708 RMVar_ID_94708 Human_SNP_ID_418534721 m1A Human chr9 + 137590452 137590452 137590452 TCGGGCCTCCGCCGCCGCCTCGCGCCCGCCGGACCTGCCACGCGCCGCCGCCGCCGCCGCCACCG TCGGGCCTCCGCCGCCGCCTCGCGCCCGCCGGCCCTGCCACGCGCCGCCGCCGCCGCCGCCACCG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:137590373..137590490 26863410 MeRIP-seq:(Medium) rs890798794 Functional Loss SNV dbSNP153 33..33 33 - - - 94709 RMVar_ID_94709 Human_SNP_ID_418534932 m1A Human chr9 - 137590792 137590792 137590792 GCGAAAAGCAGCCAGCTCGCAGAGCTCCACGGACCCGGCGCGAGTCCCCAGCCACACTCCGCACT GCGAAAAGCAGCCAGCTCGCAGAGCTCCACGGGCCCGGCGCGAGTCCCCAGCCACACTCCGCACT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr9:137590762..137590888;chr9:137590778..137590888 26863196 MeRIP-seq:(Medium) rs1288555743 Functional Loss SNV dbSNP153 33..33 33 - - - 94710 RMVar_ID_94710 Human_SNP_ID_418539745 m1A Human chr9 - 137605719 137605719 137605719 TCAGGCTGATCTCGAAGAGCTGCACTCGCCCCATGCCGCGGCCTCACCGGCCAGCCGCGCAGCGA TCAGGCTGATCTCGAAGAGCTGCACTCGCCCCTTGCCGCGGCCTCACCGGCCAGCCGCGCAGCGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137605672..137611467 26863196 MeRIP-seq:(Medium) rs1564497714 Functional Loss SNV dbSNP153 33..33 33 - - - 94711 RMVar_ID_94711 Human_SNP_ID_418539759 m1A Human chr9 + 137605740 137605740 137605740 AGGCCGCGGCATGGGGCGAGTGCAGCTCTTCGAGATCAGCCTGAGCCACGGCCGCGTCGTCTACA AGGCCGCGGCATGGGGCGAGTGCAGCTCTTCGGGATCAGCCTGAGCCACGGCCGCGTCGTCTACA A G ARRDC1 Ensembl:ENSG00000197070 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137605691..137605793 26863196 MeRIP-seq:(Medium) rs1428363150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036631,Human_RBP_ID_18427270 Human_Splice_Rec_1104457,Human_Splice_Rec_1104467,Human_Splice_Rec_1104481,Human_Splice_Rec_1104489,Human_Splice_Rec_1104493,Human_Splice_Rec_1104505,Human_Splice_Rec_1104511,Human_Splice_Rec_1104519,Human_Splice_Rec_1104557 Human_miRNA_ID_679507,Human_miRNA_ID_2027263,Human_miRNA_ID_2269407 RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 94712 RMVar_ID_94712 Human_SNP_ID_418539779 m1A Human chr9 + 137605770 137605770 137605770 CGAGATCAGCCTGAGCCACGGCCGCGTCGTCTACAGCCCCGGGGAGCCGTTGGCTGGGACCGTGC CGAGATCAGCCTGAGCCACGGCCGCGTCGTCTGCAGCCCCGGGGAGCCGTTGGCTGGGACCGTGC A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137605678..137605770 26863410 MeRIP-seq:(Medium) rs1460193161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_846328,Human_RBP_ID_5023101 Human_Splice_Rec_1104457,Human_Splice_Rec_1104467,Human_Splice_Rec_1104481,Human_Splice_Rec_1104489,Human_Splice_Rec_1104493,Human_Splice_Rec_1104505,Human_Splice_Rec_1104511,Human_Splice_Rec_1104519,Human_Splice_Rec_1104557 RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 94713 RMVar_ID_94713 Human_SNP_ID_418541563 m1A Human chr9 + 137611684 137611684 137611684 GCCCTGGCAGCGCCCGGGGGTAGAGGGCGTGCAGCAGGAAGCAAGGGCCACCCTCAGGGATGGGG GCCCTGGCAGCGCCCGGGGGTAGAGGGCGTGCGGCAGGAAGCAAGGGCCACCCTCAGGGATGGGG A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:137611640..137611775 26863196 MeRIP-seq:(Medium) rs1056996509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 94714 RMVar_ID_94714 Human_SNP_ID_418542884 m1A Human chr9 + 137614769 137614766 137614769 GCCCCCACTTCTTGGACCCCGTCTTCCTCTCCACCAAGAGCCATTCGCAGCGGCAGCCCCTGCTG GCCCCCACTTCTTGGACCCCGTCTTCCTCT___CCAAGAGCCATTCGCAGCGGCAGCCCCTGCTG TCCA T ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137614719..137614950 26863196 MeRIP-seq:(Medium) rs777781156 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3911435,Human_RBP_ID_5107228,Human_RBP_ID_27134595 RMVar_hsa_circ_120864,RMVar_hsa_circ_261051 94715 RMVar_ID_94715 Human_SNP_ID_418542886 m1A Human chr9 + 137614769 137614769 137614769 GCCCCCACTTCTTGGACCCCGTCTTCCTCTCCACCAAGAGCCATTCGCAGCGGCAGCCCCTGCTG GCCCCCACTTCTTGGACCCCGTCTTCCTCTCCCCCAAGAGCCATTCGCAGCGGCAGCCCCTGCTG A C ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137614719..137614950 26863196 MeRIP-seq:(Medium) rs1178011742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3911435,Human_RBP_ID_5107228,Human_RBP_ID_27134595 RMVar_hsa_circ_120864,RMVar_hsa_circ_261051 94716 RMVar_ID_94716 Human_SNP_ID_418542893 m1A Human chr9 + 137614785 137614785 137614785 CCCCGTCTTCCTCTCCACCAAGAGCCATTCGCAGCGGCAGCCCCTGCTGGCCACCTTGAGTTCTG CCCCGTCTTCCTCTCCACCAAGAGCCATTCGCGGCGGCAGCCCCTGCTGGCCACCTTGAGTTCTG A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137614739..137614950 26863196 MeRIP-seq:(Medium) rs377668499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715999,Human_RBP_ID_3911435,Human_RBP_ID_19144564 Human_miRNA_ID_2221581,Human_miRNA_ID_2484636,Human_miRNA_ID_3073012 RMVar_hsa_circ_120864,RMVar_hsa_circ_261051 94717 RMVar_ID_94717 Human_SNP_ID_418543425 m1A Human chr9 + 137616047 137616047 137616047 TTCTCCTTTAGGGCGAAGGGGTGACTGTGGCTAGGTTTGTCAGTTACCTTATCTATAAAATGCAC TTCTCCTTTAGGGCGAAGGGGTGACTGTGGCTCGGTTTGTCAGTTACCTTATCTATAAAATGCAC A C AL590627.3 Ensembl:ENSG00000283411 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137615996..137616091 26863196 MeRIP-seq:(Medium) rs144180383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120864,RMVar_hsa_circ_261051 94718 RMVar_ID_94718 Human_SNP_ID_418544308 m1A Human chr9 - 137618795 137618795 137618795 CGGAACCGGAACGCGCGCCCGCGGGGTAGGAGACCTGGAGCTGGAGAACCCGCCCGCCAGAGTCG CGGAACCGGAACGCGCGCCCGCGGGGTAGGAGTCCTGGAGCTGGAGAACCCGCCCGCCAGAGTCG T A ARRDC1-AS1 Ensembl:ENSG00000203993 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137618737..137618833 26863410 MeRIP-seq:(Medium) rs996240393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_716013,Human_RBP_ID_846341,Human_RBP_ID_5023251,Human_RBP_ID_5107012,Human_RBP_ID_5229736,Human_RBP_ID_5636762,Human_RBP_ID_18427716,Human_RBP_ID_23094898,Human_RBP_ID_27374000 94719 RMVar_ID_94719 Human_SNP_ID_418544595 m1A Human chr9 + 137619312 137619312 137619312 CGGGCGGCGGCTGGGGGAGCGGGCGGGGGCGCAGGTGAGGGAGGCGACCGCGTACCTGTGCCCGC CGGGCGGCGGCTGGGGGAGCGGGCGGGGGCGCGGGTGAGGGAGGCGACCGCGTACCTGTGCCCGC A G AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137619295..137619439 26863196 MeRIP-seq:(Medium) rs1291414777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224465,Human_RBP_ID_9339823,Human_RBP_ID_9355142,Human_RBP_ID_18467765,Human_RBP_ID_26796292 RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056 94720 RMVar_ID_94720 Human_SNP_ID_418558609 m1A Human chr9 + 137669416 137669385 137669416 ACCCAAGACGCCCCCCACAGCACGTGCACTCCACGACTGCACCCAAGACGCCGCCCACAGCACGT AC_______________________________CGACTGCACCCAAGACGCCGCCCACAGCACGT CCCAAGACGCCCCCCACAGCACGTGCACTCCA C AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137669363..137669546 26863196 MeRIP-seq:(Medium) rs1332610788 Functional Loss DEL dbSNP153 3..33 33 - - - Human_RBP_ID_219255,Human_RBP_ID_255643,Human_RBP_ID_3911446,Human_RBP_ID_5107245,Human_RBP_ID_5135436,Human_RBP_ID_17094855,Human_RBP_ID_24537666,Human_RBP_ID_24555508,Human_RBP_ID_27843804 RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056 94721 RMVar_ID_94721 Human_SNP_ID_418558618 m1A Human chr9 + 137669400 137669400 137669400 ACGTGCACTGGACTCCACCCAAGACGCCCCCCACAGCACGTGCACTCCACGACTGCACCCAAGAC ACGTGCACTGGACTCCACCCAAGACGCCCCCCTCAGCACGTGCACTCCACGACTGCACCCAAGAC A T AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137669284..137669571 26863196 MeRIP-seq:(Medium) rs10867044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219255,Human_RBP_ID_3911446,Human_RBP_ID_5107245,Human_RBP_ID_5135436,Human_RBP_ID_17095025,Human_RBP_ID_24537666,Human_RBP_ID_24555508,Human_RBP_ID_27843804 RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056 94722 RMVar_ID_94722 Human_SNP_ID_418558623 m1A Human chr9 + 137669416 137669413 137669416 ACCCAAGACGCCCCCCACAGCACGTGCACTCCACGACTGCACCCAAGACGCCGCCCACAGCACGT ACCCAAGACGCCCCCCACAGCACGTGCACT___CGACTGCACCCAAGACGCCGCCCACAGCACGT TCCA T AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137669363..137669546 26863196 MeRIP-seq:(Medium) rs57396533 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_219255,Human_RBP_ID_255643,Human_RBP_ID_3911446,Human_RBP_ID_5107245,Human_RBP_ID_5135436,Human_RBP_ID_17094855,Human_RBP_ID_24537666,Human_RBP_ID_24555508,Human_RBP_ID_27843804 RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056 94723 RMVar_ID_94723 Human_SNP_ID_418558630 m1A Human chr9 + 137669416 137669416 137669416 ACCCAAGACGCCCCCCACAGCACGTGCACTCCACGACTGCACCCAAGACGCCGCCCACAGCACGT ACCCAAGACGCCCCCCACAGCACGTGCACTCCCCGACTGCACCCAAGACGCCGCCCACAGCACGT A C AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137669363..137669546 26863196 MeRIP-seq:(Medium) rs1017138715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219255,Human_RBP_ID_255643,Human_RBP_ID_3911446,Human_RBP_ID_5107245,Human_RBP_ID_5135436,Human_RBP_ID_17094855,Human_RBP_ID_24537666,Human_RBP_ID_24555508,Human_RBP_ID_27843804 RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056 94724 RMVar_ID_94724 Human_SNP_ID_418570388 m1A Human chr9 - 137710990 137710990 137710990 AGCAGCTCGGTTTTCACACAGCAATCCTGCTGAGGCTCCCCCCTCGCCGGAACTGCCTGTTAGAG AGCAGCTCGGTTTTCACACAGCAATCCTGCTGGGGCTCCCCCCTCGCCGGAACTGCCTGTTAGAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:137710980..137711073 26863410 MeRIP-seq:(Medium) rs749617180 Functional Loss SNV dbSNP153 33..33 33 - - - 94725 RMVar_ID_94725 Human_SNP_ID_418572028 m1A Human chr9 - 137716362 137716360 137716363 ACCAACACAACTTCCTCCCCCACCATGACACCACAACTTCCTCCCCCACCATGACACCACCACAA ACCAACACAACTTCCTCCCCCACCATGACAC___AACTTCCTCCCCCACCATGACACCACCACAA TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137716308..137716407 26863196 MeRIP-seq:(Medium) rs1310093322 Functional Loss DEL dbSNP153 32..34 33 - - - 94726 RMVar_ID_94726 Human_SNP_ID_418572184 m1A Human chr9 - 137716645 137716645 137716645 GCCTCTCCTGCCTGTTTCTCTGCTGAGCCTTCATCGGCAGCCATAGGTGTCTCTGCCAACAAAGA GCCTCTCCTGCCTGTTTCTCTGCTGAGCCTTCTTCGGCAGCCATAGGTGTCTCTGCCAACAAAGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137716612..137716693 26863196 MeRIP-seq:(Medium) rs1308596650 Functional Loss SNV dbSNP153 33..33 33 - - - 94727 RMVar_ID_94727 Human_SNP_ID_418572185 m1A Human chr9 - 137716645 137716645 137716645 GCCTCTCCTGCCTGTTTCTCTGCTGAGCCTTCATCGGCAGCCATAGGTGTCTCTGCCAACAAAGA GCCTCTCCTGCCTGTTTCTCTGCTGAGCCTTCGTCGGCAGCCATAGGTGTCTCTGCCAACAAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137716612..137716693 26863196 MeRIP-seq:(Medium) rs1308596650 Functional Loss SNV dbSNP153 33..33 33 - - - 94728 RMVar_ID_94728 Human_SNP_ID_418572210 m1A Human chr9 + 137716680 137716680 137716680 AGGCTCAGCAGAGAAACAGGCAGGAGAGGCCCACATGGCTGCGGACGGTGAGACCAATGGGTCTT AGGCTCAGCAGAGAAACAGGCAGGAGAGGCCCGCATGGCTGCGGACGGTGAGACCAATGGGTCTT A G EHMT1 Ensembl:ENSG00000181090 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137716602..137716730 26863196 MeRIP-seq:(Medium) rs1177732855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964354,Human_RBP_ID_5023275,Human_RBP_ID_5482454,Human_RBP_ID_9407869,Human_RBP_ID_18414481,Human_RBP_ID_19026392,Human_RBP_ID_26240718,Human_RBP_ID_26361564,Human_RBP_ID_27832953 Human_Splice_Rec_1104570,Human_Splice_Rec_1104598,Human_Splice_Rec_1104632,Human_Splice_Rec_1104636,Human_Splice_Rec_1104688,Human_Splice_Rec_1104694,Human_Splice_Rec_1104718,Human_Splice_Rec_1104758,Human_Splice_Rec_1104762,Human_Splice_Rec_1104770,Human_Splice_Rec_1104822,Human_Splice_Rec_1104826,Human_Splice_Rec_1104872,Human_Splice_Rec_1104890 Human_miRNA_ID_2297361 RMVar_hsa_circ_11273,RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_125105,RMVar_hsa_circ_261057,RMVar_hsa_circ_261059,RMVar_hsa_circ_81510,RMVar_hsa_circ_261058,RMVar_hsa_circ_261056,RMVar_hsa_circ_103423,RMVar_hsa_circ_296362,RMVar_hsa_circ_367520,RMVar_hsa_circ_375633,RMVar_hsa_circ_299059,RMVar_hsa_circ_295981,RMVar_hsa_circ_58621,RMVar_hsa_circ_93074,RMVar_hsa_circ_19449,RMVar_hsa_circ_39019,RMVar_hsa_circ_261063,RMVar_hsa_circ_261065,RMVar_hsa_circ_261066,RMVar_hsa_circ_261067,RMVar_hsa_circ_261064,RMVar_hsa_circ_316781,RMVar_hsa_circ_318929,RMVar_hsa_circ_261062,RMVar_hsa_circ_356217,RMVar_hsa_circ_316808,RMVar_hsa_circ_278047,RMVar_hsa_circ_286764,RMVar_hsa_circ_275498,RMVar_hsa_circ_261068,RMVar_hsa_circ_261070,RMVar_hsa_circ_261071,RMVar_hsa_circ_261072,RMVar_hsa_circ_261069 94729 RMVar_ID_94729 Human_SNP_ID_418574909 m1A Human chr9 - 137723262 137723262 137723262 CACCCCGGGCTCAGGCCCAGAACCACAGACACAGGCACACCCCGGGCTCAGGCCCAGAACCACGG CACCCCGGGCTCAGGCCCAGAACCACAGACACGGGCACACCCCGGGCTCAGGCCCAGAACCACGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137723186..137723299 26863196 MeRIP-seq:(Medium) rs1375031398 Functional Loss SNV dbSNP153 33..33 33 - - - 94730 RMVar_ID_94730 Human_SNP_ID_418582512 m1A Human chr9 + 137750746 137750746 137750746 GGGACTGTGCACAGTGGGGGACACCGGAGCTCAGGACGTGGCTGCCGGAGGGGGCGCGGCTGCCG GGGACTGTGCACAGTGGGGGACACCGGAGCTCGGGACGTGGCTGCCGGAGGGGGCGCGGCTGCCG A G EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137750744..137750838 26863196 MeRIP-seq:(Medium) rs3123513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7908952 GWAS_ID_12467,GWAS_ID_12468 RMVar_hsa_circ_11273,RMVar_hsa_circ_106451,RMVar_hsa_circ_123156,RMVar_hsa_circ_261059,RMVar_hsa_circ_261058,RMVar_hsa_circ_103423,RMVar_hsa_circ_367520,RMVar_hsa_circ_375633,RMVar_hsa_circ_58621,RMVar_hsa_circ_93074,RMVar_hsa_circ_23265,RMVar_hsa_circ_39019,RMVar_hsa_circ_261063,RMVar_hsa_circ_261064,RMVar_hsa_circ_316781,RMVar_hsa_circ_318929,RMVar_hsa_circ_261062,RMVar_hsa_circ_356217,RMVar_hsa_circ_278047,RMVar_hsa_circ_261070,RMVar_hsa_circ_261071,RMVar_hsa_circ_261072,RMVar_hsa_circ_296556,RMVar_hsa_circ_349919,RMVar_hsa_circ_359399,RMVar_hsa_circ_286330,RMVar_hsa_circ_116934,RMVar_hsa_circ_121088,RMVar_hsa_circ_72224,RMVar_hsa_circ_261082,RMVar_hsa_circ_261073,RMVar_hsa_circ_261075,RMVar_hsa_circ_261077,RMVar_hsa_circ_261076,RMVar_hsa_circ_261074,RMVar_hsa_circ_273196,RMVar_hsa_circ_331067,RMVar_hsa_circ_334300,RMVar_hsa_circ_313864,RMVar_hsa_circ_261083,RMVar_hsa_circ_31834,RMVar_hsa_circ_261081,RMVar_hsa_circ_294215,RMVar_hsa_circ_311965,RMVar_hsa_circ_54563,RMVar_hsa_circ_261084,RMVar_hsa_circ_261085 94731 RMVar_ID_94731 Human_SNP_ID_418590440 m1A Human chr9 - 137779469 137779469 137779469 TGAAGGCTGGAAGGCCCGGCAGACGTCTGCCCACCAGCCCCACAAGCTCAAGTGCAAACCCACCA TGAAGGCTGGAAGGCCCGGCAGACGTCTGCCCGCCAGCCCCACAAGCTCAAGTGCAAACCCACCA T C AL590627.1 Ensembl:ENSG00000255585 Pseudogene intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137779463..137779584 32194978 MeRIP-seq:(Medium) rs1157392900 Functional Loss SNV dbSNP153 33..33 33 - - - 94732 RMVar_ID_94732 Human_SNP_ID_418590777 m1A Human chr9 - 137780376 137780374 137780376 AGCGTCATCACCACACATCCCAGCGTCATCACACGTCTCAGCGTCATCACCACACGTCTCAGCGT AGCGTCATCACCACACATCCCAGCGTCATCACCCATCTCAGCGTCATCACCACACGTCTCAGCGT CGT TGG AL590627.1 Ensembl:ENSG00000255585 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:137780042..137780421;chr9:137780049..137780441;chr9:137780033..137780430 26863196 MeRIP-seq:(Medium) rs796673909 Functional Loss MNV dbSNP153 33..35 33 - - - 94733 RMVar_ID_94733 Human_SNP_ID_418590781 m1A Human chr9 - 137780376 137780376 137780376 AGCGTCATCACCACACATCCCAGCGTCATCACACGTCTCAGCGTCATCACCACACGTCTCAGCGT AGCGTCATCACCACACATCCCAGCGTCATCACCCGTCTCAGCGTCATCACCACACGTCTCAGCGT T G AL590627.1 Ensembl:ENSG00000255585 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:137780042..137780421;chr9:137780049..137780441;chr9:137780033..137780430 26863196 MeRIP-seq:(Medium) rs62589683 Functional Loss SNV dbSNP153 33..33 33 - - - 94734 RMVar_ID_94734 Human_SNP_ID_418590876 m1A Human chr9 + 137780566 137780566 137780566 TGACGCTGAGATGTGTGGTGATGGCATCACTGAGATGTGTGGTGATGACGCTGGGATGTGTGGTG TGACGCTGAGATGTGTGGTGATGGCATCACTGGGATGTGTGGTGATGACGCTGGGATGTGTGGTG A G EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137780517..137780601 26863196 MeRIP-seq:(Medium) rs1251218754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22338905,Human_RBP_ID_24294024 RMVar_hsa_circ_6821,RMVar_hsa_circ_11273,RMVar_hsa_circ_123156,RMVar_hsa_circ_261059,RMVar_hsa_circ_103423,RMVar_hsa_circ_58621,RMVar_hsa_circ_23265,RMVar_hsa_circ_39019,RMVar_hsa_circ_318929,RMVar_hsa_circ_261062,RMVar_hsa_circ_116934,RMVar_hsa_circ_72224,RMVar_hsa_circ_261073,RMVar_hsa_circ_261074,RMVar_hsa_circ_313864,RMVar_hsa_circ_31834,RMVar_hsa_circ_261085,RMVar_hsa_circ_360394,RMVar_hsa_circ_107097,RMVar_hsa_circ_111115,RMVar_hsa_circ_87517,RMVar_hsa_circ_83777,RMVar_hsa_circ_82547,RMVar_hsa_circ_261086,RMVar_hsa_circ_261088,RMVar_hsa_circ_261089,RMVar_hsa_circ_261087,RMVar_hsa_circ_332958,RMVar_hsa_circ_353080,RMVar_hsa_circ_285505,RMVar_hsa_circ_261096,RMVar_hsa_circ_261097,RMVar_hsa_circ_261095,RMVar_hsa_circ_107071,RMVar_hsa_circ_261098,RMVar_hsa_circ_41490,RMVar_hsa_circ_57287,RMVar_hsa_circ_261099,RMVar_hsa_circ_288081,RMVar_hsa_circ_261102,RMVar_hsa_circ_372908,RMVar_hsa_circ_327999,RMVar_hsa_circ_99787,RMVar_hsa_circ_285558,RMVar_hsa_circ_92204,RMVar_hsa_circ_71271,RMVar_hsa_circ_104125,RMVar_hsa_circ_261104,RMVar_hsa_circ_261106,RMVar_hsa_circ_261107,RMVar_hsa_circ_261105,RMVar_hsa_circ_261103,RMVar_hsa_circ_273236,RMVar_hsa_circ_261110,RMVar_hsa_circ_88014,RMVar_hsa_circ_91749,RMVar_hsa_circ_261112,RMVar_hsa_circ_75840,RMVar_hsa_circ_261111,RMVar_hsa_circ_261108,RMVar_hsa_circ_261109,RMVar_hsa_circ_98690,RMVar_hsa_circ_12813,RMVar_hsa_circ_30197,RMVar_hsa_circ_268157,RMVar_hsa_circ_376114,RMVar_hsa_circ_261113,RMVar_hsa_circ_308809,RMVar_hsa_circ_261114 94735 RMVar_ID_94735 Human_SNP_ID_418590943 m1A Human chr9 - 137780722 137780722 137780722 TCACCACACATCCCAGTGTCATCACCACACATACCGGCGTCATCACCACACGTCTCGGCGTCATC TCACCACACATCCCAGTGTCATCACCACACATCCCGGCGTCATCACCACACGTCTCGGCGTCATC T G AL590627.1 Ensembl:ENSG00000255585 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137780685..137780774 26863196 MeRIP-seq:(Medium) rs62589686 Functional Loss SNV dbSNP153 33..33 33 - - - 94736 RMVar_ID_94736 Human_SNP_ID_418592290 m1A Human chr9 - 137784795 137784795 137784795 CATGGAGCTGGCCCCCAGTGCCCCCAGTGCCTACCTCGGCTCAGCGCTTCTCACGGCACACTTTC CATGGAGCTGGCCCCCAGTGCCCCCAGTGCCTGCCTCGGCTCAGCGCTTCTCACGGCACACTTTC T C AL590627.1 Ensembl:ENSG00000255585 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137784792..137784876 26863196 MeRIP-seq:(Medium) rs1434791575 Functional Loss SNV dbSNP153 33..33 33 - - - 94737 RMVar_ID_94737 Human_SNP_ID_418602471 m1A Human chr9 + 137818513 137818513 137818513 GGGCGCCGTGTACCAAGACTGTAGAGAGGCTGAGGGGGGGCGCCATGTACCGAGACTGTAGAGAG GGGCGCCGTGTACCAAGACTGTAGAGAGGCTGTGGGGGGGCGCCATGTACCGAGACTGTAGAGAG A T EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:137818480..137818593 26863196 MeRIP-seq:(Medium) rs866503342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5244087,Human_RBP_ID_16626090,Human_RBP_ID_24443327 RMVar_hsa_circ_75840,RMVar_hsa_circ_261108,RMVar_hsa_circ_268157,RMVar_hsa_circ_115754,RMVar_hsa_circ_261127,RMVar_hsa_circ_101253,RMVar_hsa_circ_261129 94738 RMVar_ID_94738 Human_SNP_ID_418602853 m1A Human chr9 + 137819580 137819580 137819580 GCCGTGTACCGAGACCGTAGAGAGGCCGACTGAGGGGCGCCGTGTACCGAGACTGTAGAGAGGCC GCCGTGTACCGAGACCGTAGAGAGGCCGACTGGGGGGCGCCGTGTACCGAGACTGTAGAGAGGCC A G EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137819561..137819634 26863196 MeRIP-seq:(Medium) rs1218621467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227569,Human_RBP_ID_16626095,Human_RBP_ID_17437421 RMVar_hsa_circ_75840,RMVar_hsa_circ_261108,RMVar_hsa_circ_268157,RMVar_hsa_circ_115754,RMVar_hsa_circ_261127,RMVar_hsa_circ_101253,RMVar_hsa_circ_261129 94739 RMVar_ID_94739 Human_SNP_ID_418607726 m1A Human chr9 + 137834895 137834886 137834895 CCTGGCCCAGCGTCAGGCCAGCGCGGCCCAGGAGGCCCAGGAGGACGGCTTGCCCGACACCAGCT CCTGGCCCAGCGTCAGGCCAGCGC_________GGCCCAGGAGGACGGCTTGCCCGACACCAGCT CGGCCCAGGA C EHMT1 Ensembl:ENSG00000181090 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137834844..137834954 26863196 MeRIP-seq:(Medium) rs751283937 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_75840,RMVar_hsa_circ_261108,RMVar_hsa_circ_268157,RMVar_hsa_circ_261130 94740 RMVar_ID_94740 Human_SNP_ID_418607954 m1A Human chr9 + 137835427 137835427 137835427 CGCCCTGCCCACGGCCTGCGTGGCTGGGGCCGAGTCCCAGGGGCCGCACGGAGGGCACAGTCTCC CGCCCTGCCCACGGCCTGCGTGGCTGGGGCCGTGTCCCAGGGGCCGCACGGAGGGCACAGTCTCC A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1009907478 Functional Loss SNV dbSNP153 33..33 33 - - - 94741 RMVar_ID_94741 Human_SNP_ID_418703231 m1A Human chr9 + 138176986 138176986 138176986 CTGACTGGTTCCCCGACAACGTAAAAACAGCCATCTGTGACATCCCACCCCGGGGGCTAAAAATG CTGACTGGTTCCCCGACAACGTAAAAACAGCCGTCTGTGACATCCCACCCCGGGGGCTAAAAATG A G TUBBP5 Ensembl:ENSG00000159247 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7869352 Functional Loss SNV dbSNP153 33..33 33 - - - 94742 RMVar_ID_94742 Human_SNP_ID_305218629 m1A Human chr6 + 165624160 165624160 165624160 CAAGCTTTGAGTCATATCCATCCACCTCTCACAAGAGTTCCCACAAGAACTGTCCCTCCTCTGGC CAAGCTTTGAGTCATATCCATCCACCTCTCACGAGAGTTCCCACAAGAACTGTCCCTCCTCTGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165624153..165624336 26863196 MeRIP-seq:(Medium) rs1204742499 Functional Loss SNV dbSNP153 33..33 33 - - - 94743 RMVar_ID_94743 Human_SNP_ID_305226607 m1A Human chr6 - 165654248 165654248 165654248 GGAACAGGACAATGAGGAGGATGACGGGAGTGACTGGGAACGTTTTAGAAGGAAAGTGATGCAAT GGAACAGGACAATGAGGAGGATGACGGGAGTGGCTGGGAACGTTTTAGAAGGAAAGTGATGCAAT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165654198..165654336 26863196 MeRIP-seq:(Medium) rs1361428473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18858483 94744 RMVar_ID_94744 Human_SNP_ID_305226797 m1A Human chr6 - 165654926 165654926 165654926 AGTCGGAGGATAGGACAGAAGAAGGCAGAGCCATGGAGCACCCTGGAGAGGTGTGACCCGGCAAG AGTCGGAGGATAGGACAGAAGAAGGCAGAGCCTTGGAGCACCCTGGAGAGGTGTGACCCGGCAAG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165654810..165654963 26863196 MeRIP-seq:(Medium) rs1193948759 Functional Loss SNV dbSNP153 33..33 33 - - - 94745 RMVar_ID_94745 Human_SNP_ID_305227000 m1A Human chr6 + 165655525 165655524 165655526 GTCCCCATATCCAACCCACCTGCAGGTCTTATACACGCCACCTCCAAACACCTCCTGAACCACCG GTCCCCATATCCAACCCACCTGCAGGTCTTAT__ACGCCACCTCCAAACACCTCCTGAACCACCG TAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:165655312..165655632;chr6:165655320..165655643 26863196 MeRIP-seq:(Medium) rs200377113 Functional Loss DEL dbSNP153 33..34 33 - - - 94746 RMVar_ID_94746 Human_SNP_ID_305227362 m1A Human chr6 - 165656363 165656363 165656363 GAGATACAAGCAGGAGGTAGCAGTTAATAGTCACACATCCAGGTGGCTGGTTGGATAAGGCAGGA GAGATACAAGCAGGAGGTAGCAGTTAATAGTCGCACATCCAGGTGGCTGGTTGGATAAGGCAGGA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165656313..165656511 26863196 MeRIP-seq:(Medium) rs548430193 Functional Loss SNV dbSNP153 33..33 33 - - - 94747 RMVar_ID_94747 Human_SNP_ID_305229182 m1A Human chr6 + 165662295 165662295 165662295 GCCGCGGTGACTACTGCTGGTGGGGACGCTCAAGGGAGCTGCCTCTTGTCCTCCTCCTCCTCCTC GCCGCGGTGACTACTGCTGGTGGGGACGCTCAGGGGAGCTGCCTCTTGTCCTCCTCCTCCTCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165662247..165662351 26863196 MeRIP-seq:(Medium) rs1281009120 Functional Loss SNV dbSNP153 33..33 33 - - - 94748 RMVar_ID_94748 Human_SNP_ID_305229257 m1A Human chr6 + 165662430 165662430 165662430 GAGGTGAAAGGCAGATGAGGAGGGGAGAAAAGAGGGAGGGGGCGGGGGGGGCGGCGGCCAGAAGT GAGGTGAAAGGCAGATGAGGAGGGGAGAAAAGGGGGAGGGGGCGGGGGGGGCGGCGGCCAGAAGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:165662306..165662527 26863196 MeRIP-seq:(Medium) rs1404943271 Functional Loss SNV dbSNP153 33..33 33 - - - 94749 RMVar_ID_94749 Human_SNP_ID_305241366 m1A Human chr6 - 165709103 165709103 165709103 GGGAGCATGGAGGCGGAAAGTGTGGGGAGAGCACGGCAGCATGTGGGTGGAGAGTGGGAGGAAGA GGGAGCATGGAGGCGGAAAGTGTGGGGAGAGCGCGGCAGCATGTGGGTGGAGAGTGGGAGGAAGA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165709022..165709416 26863196 MeRIP-seq:(Medium) rs1405255057 Functional Loss SNV dbSNP153 33..33 33 - - - 94750 RMVar_ID_94750 Human_SNP_ID_305241468 m1A Human chr6 + 165709318 165709318 165709318 CTCTCCCCACCATGCTGCGGCGCTCTCCCCCCACTCCACCGCTATGCTGTGGTGCTCTCTCCCCA CTCTCCCCACCATGCTGCGGCGCTCTCCCCCCCCTCCACCGCTATGCTGTGGTGCTCTCTCCCCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165709236..165709401 26863196 MeRIP-seq:(Medium) rs577904135 Functional Loss SNV dbSNP153 33..33 33 - - - 94751 RMVar_ID_94751 Human_SNP_ID_305241469 m1A Human chr6 + 165709318 165709318 165709318 CTCTCCCCACCATGCTGCGGCGCTCTCCCCCCACTCCACCGCTATGCTGTGGTGCTCTCTCCCCA CTCTCCCCACCATGCTGCGGCGCTCTCCCCCCTCTCCACCGCTATGCTGTGGTGCTCTCTCCCCA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165709236..165709401 26863196 MeRIP-seq:(Medium) rs577904135 Functional Loss SNV dbSNP153 33..33 33 - - - 94752 RMVar_ID_94752 Human_SNP_ID_305241634 m1A Human chr6 - 165709602 165709602 165709602 GGCAGCATGGGGGTGTAGAGTGGAGGGAGCACAGCAGCATGGAGGTGGAGAGTGTGGGGGATAGC GGCAGCATGGGGGTGTAGAGTGGAGGGAGCACGGCAGCATGGAGGTGGAGAGTGTGGGGGATAGC T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165709556..165709919 26863196 MeRIP-seq:(Medium) rs1429165694 Functional Loss SNV dbSNP153 33..33 33 - - - 94753 RMVar_ID_94753 Human_SNP_ID_305252058 m1A Human chr6 + 165749230 165749228 165749230 ATCACCATCATCACCATCACCATCATATCACCATCACCACCATCACATCACCATCATCACCATTA ATCACCATCATCACCATCACCATCATATCAC__TCACCACCATCACATCACCATCATCACCATTA CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165749132..165749510 26863196 MeRIP-seq:(Medium) rs1417562284 Functional Loss DEL dbSNP153 32..33 33 - - - 94754 RMVar_ID_94754 Human_SNP_ID_305252197 m1A Human chr6 + 165749385 165749379 165749386 TCACCATCACCATCATCACCATCACCACCACCATCATCACCATTACCATCAACACCATCACCATC TCACCATCACCATCATCACCATCACCA_______CATCACCATTACCATCAACACCATCACCATC ACCACCAT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165749340..165749449 26863196 MeRIP-seq:(Medium) rs1562717455 Functional Loss DEL dbSNP153 28..34 33 - - - 94755 RMVar_ID_94755 Human_SNP_ID_305252201 m1A Human chr6 + 165749385 165749380 165749386 TCACCATCACCATCATCACCATCACCACCACCATCATCACCATTACCATCAACACCATCACCATC TCACCATCACCATCATCACCATCACCAC______CATCACCATTACCATCAACACCATCACCATC CCACCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165749340..165749449 26863196 MeRIP-seq:(Medium) rs1562717463 Functional Loss DEL dbSNP153 29..34 33 - - - 94756 RMVar_ID_94756 Human_SNP_ID_305252209 m1A Human chr6 + 165749385 165749383 165749386 TCACCATCACCATCATCACCATCACCACCACCATCATCACCATTACCATCAACACCATCACCATC TCACCATCACCATCATCACCATCACCACCAC___CATCACCATTACCATCAACACCATCACCATC CCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165749340..165749449 26863196 MeRIP-seq:(Medium) rs1409248015 Functional Loss DEL dbSNP153 32..34 33 - - - 94757 RMVar_ID_94757 Human_SNP_ID_305252261 m1A Human chr6 + 165749459 165749441 165749460 ACCACCATCACCATCACCACCATCACATCACCATCATCAACAACACCATCAACACCATCATCACC ACCACCATCACCATC___________________CATCAACAACACCATCAACACCATCATCACC CACCACCATCACATCACCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165749184..165749493 26863196 MeRIP-seq:(Medium) rs1240369038 Functional Loss DEL dbSNP153 16..34 33 - - - 94758 RMVar_ID_94758 Human_SNP_ID_305252274 m1A Human chr6 + 165749459 165749457 165749460 ACCACCATCACCATCACCACCATCACATCACCATCATCAACAACACCATCAACACCATCATCACC ACCACCATCACCATCACCACCATCACATCAC___CATCAACAACACCATCAACACCATCATCACC CCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165749184..165749493 26863196 MeRIP-seq:(Medium) rs1325000220 Functional Loss DEL dbSNP153 32..34 33 - - - 94759 RMVar_ID_94759 Human_SNP_ID_305252279 m1A Human chr6 - 165749463 165749463 165749463 TGATGGTGATGATGGTGTTGATGGTGTTGTTGATGATGGTGATGTGATGGTGGTGATGGTGATGG TGATGGTGATGATGGTGTTGATGGTGTTGTTGGTGATGGTGATGTGATGGTGGTGATGGTGATGG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165749148..165749527 26863196 MeRIP-seq:(Medium) rs1386820845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24147005 94760 RMVar_ID_94760 Human_SNP_ID_305262758 m1A Human chr6 - 165792158 165792158 165792158 GGTGGATGAGGGCAAGTGGGGCAGGGGCGAACATTGCAGGCCCGAGAAGCAGCAGGTGTGGGAAT GGTGGATGAGGGCAAGTGGGGCAGGGGCGAACGTTGCAGGCCCGAGAAGCAGCAGGTGTGGGAAT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165792107..165792172 26863196 MeRIP-seq:(Medium) rs900811637 Functional Loss SNV dbSNP153 33..33 33 - - - 94761 RMVar_ID_94761 Human_SNP_ID_305262759 m1A Human chr6 - 165792158 165792158 165792158 GGTGGATGAGGGCAAGTGGGGCAGGGGCGAACATTGCAGGCCCGAGAAGCAGCAGGTGTGGGAAT GGTGGATGAGGGCAAGTGGGGCAGGGGCGAACCTTGCAGGCCCGAGAAGCAGCAGGTGTGGGAAT T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165792107..165792172 26863196 MeRIP-seq:(Medium) rs900811637 Functional Loss SNV dbSNP153 33..33 33 - - - 94762 RMVar_ID_94762 Human_SNP_ID_305263453 m1A Human chr6 + 165794383 165794381 165794383 ACAGATGCTCACACACACTCATACAATCCCCCACACTCACACATGCTCACACTCATCACACACTC ACAGATGCTCACACACACTCATACAATCCCC__CACTCACACATGCTCACACTCATCACACACTC CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:165794107..165794644;chr6:165794079..165794675;chr6:165794079..165794666;chr6:165794117..165794681 26863196 MeRIP-seq:(Medium) rs1229520892 Functional Loss DEL dbSNP153 32..33 33 - - - 94763 RMVar_ID_94763 Human_SNP_ID_305263454 m1A Human chr6 + 165794383 165794383 165794383 ACAGATGCTCACACACACTCATACAATCCCCCACACTCACACATGCTCACACTCATCACACACTC ACAGATGCTCACACACACTCATACAATCCCCCCCACTCACACATGCTCACACTCATCACACACTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:165794107..165794644;chr6:165794079..165794675;chr6:165794079..165794666;chr6:165794117..165794681 26863196 MeRIP-seq:(Medium) rs1011128788 Functional Loss SNV dbSNP153 33..33 33 - - - 94764 RMVar_ID_94764 Human_SNP_ID_305263560 m1A Human chr6 - 165794564 165794560 165794564 GAGTGAATATGTGTGTGTAGGAATGTGTGTGTAAGTGACCTTGTGAGTGTGTAATGAGTGTGTGT GAGTGAATATGTGTGTGTAGGAATGTGTGTGT____GACCTTGTGAGTGTGTAATGAGTGTGTGT CACTT C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165794245..165794650 26863196 MeRIP-seq:(Medium) rs750303854 Functional Loss DEL dbSNP153 33..36 33 - - - 94765 RMVar_ID_94765 Human_SNP_ID_305266069 m1A Human chr6 + 165804933 165804932 165804933 GCAAGCAGAGGGGCGCACGGAGGGGAGCATGGAGGGACGTGGGGAGCATGGAGAGACGTGGGGGC GCAAGCAGAGGGGCGCACGGAGGGGAGCATGG_GGGACGTGGGGAGCATGGAGAGACGTGGGGGC GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165804690..165805137 26863196 MeRIP-seq:(Medium) rs1562745258 Functional Loss DEL dbSNP153 33..33 33 - - - 94766 RMVar_ID_94766 Human_SNP_ID_305266077 m1A Human chr6 + 165804954 165804954 165804954 GGGGAGCATGGAGGGACGTGGGGAGCATGGAGAGACGTGGGGGCGCACGGAGGGACGGCGGGGCC GGGGAGCATGGAGGGACGTGGGGAGCATGGAGGGACGTGGGGGCGCACGGAGGGACGGCGGGGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:165804605..165805200 26863196 MeRIP-seq:(Medium) rs112859373 Functional Loss SNV dbSNP153 33..33 33 - - - 94767 RMVar_ID_94767 Human_SNP_ID_305266081 m1A Human chr6 + 165804968 165804968 165804968 GACGTGGGGAGCATGGAGAGACGTGGGGGCGCACGGAGGGACGGCGGGGCCTGGAGCGAGCATAG GACGTGGGGAGCATGGAGAGACGTGGGGGCGCGCGGAGGGACGGCGGGGCCTGGAGCGAGCATAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165804676..165805101 26863196 MeRIP-seq:(Medium) rs1290129357 Functional Loss SNV dbSNP153 33..33 33 - - - 94768 RMVar_ID_94768 Human_SNP_ID_305269666 m1A Human chr6 - 165819380 165819380 165819380 GCAGGAGGTGGGGTCGGCAACTGCATCAGGCAACAGGAGCTGAGGATGAGCATCTGAATCTCTCA GCAGGAGGTGGGGTCGGCAACTGCATCAGGCAGCAGGAGCTGAGGATGAGCATCTGAATCTCTCA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165819330..165819525 26863196 MeRIP-seq:(Medium) rs1209299731 Functional Loss SNV dbSNP153 33..33 33 - - - 94769 RMVar_ID_94769 Human_SNP_ID_305271774 m1A Human chr6 - 165826450 165826450 165826450 GGGGACAGGTGGACATGGGGACAGAGAGACACAGGGACAAAGGAACGTAAGGACAGAGGGATACC GGGGACAGGTGGACATGGGGACAGAGAGACACGGGGACAAAGGAACGTAAGGACAGAGGGATACC T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165826305..165826597 26863196 MeRIP-seq:(Medium) rs531981180 Functional Loss SNV dbSNP153 33..33 33 - - - 94770 RMVar_ID_94770 Human_SNP_ID_305271816 m1A Human chr6 + 165826514 165826512 165826514 CACGTCCCTCTGTCCCTGTGTCCCTCTGTCCCAGTGTTACTCTGCCCCTGTGTCCCTCTGTCCCC CACGTCCCTCTGTCCCTGTGTCCCTCTGTCC__GTGTTACTCTGCCCCTGTGTCCCTCTGTCCCC CCA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165826263..165826600 26863196 MeRIP-seq:(Medium) rs11268670 Functional Loss DEL dbSNP153 32..33 33 - - - 94771 RMVar_ID_94771 Human_SNP_ID_305271819 m1A Human chr6 + 165826514 165826514 165826514 CACGTCCCTCTGTCCCTGTGTCCCTCTGTCCCAGTGTTACTCTGCCCCTGTGTCCCTCTGTCCCC CACGTCCCTCTGTCCCTGTGTCCCTCTGTCCCTGTGTTACTCTGCCCCTGTGTCCCTCTGTCCCC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165826263..165826600 26863196 MeRIP-seq:(Medium) rs138038543 Functional Loss SNV dbSNP153 33..33 33 - - - 94772 RMVar_ID_94772 Human_SNP_ID_305272147 m1A Human chr6 - 165827422 165827422 165827422 TTTTGTTGAATTGGAGAGACCACCACATTCCCAGGAATTACTGGGAGGAGTTCTTCTGGGAGAGT TTTTGTTGAATTGGAGAGACCACCACATTCCCGGGAATTACTGGGAGGAGTTCTTCTGGGAGAGT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165827408..165827478 26863196 MeRIP-seq:(Medium) rs191869687 Functional Loss SNV dbSNP153 33..33 33 - - - 94773 RMVar_ID_94773 Human_SNP_ID_305275281 m1A Human chr6 - 165839830 165839826 165839831 AGACAGGGATGGAGATGATAAGAATGGAGACGAGATTGGAGATGGGGATGGAGCTGGAGAAGGGG AGACAGGGATGGAGATGATAAGAATGGAGAC_____TGGAGATGGGGATGGAGCTGGAGAAGGGG AATCTC A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:165839683..165840250;chr6:165839619..165840181 26863196 MeRIP-seq:(Medium) rs1349650425 Functional Loss DEL dbSNP153 32..36 33 - - - 94774 RMVar_ID_94774 Human_SNP_ID_305275419 m1A Human chr6 - 165839944 165839927 165839945 GGATGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATG GGATGAAGACAGAGATGTAGATGGGGATGGA__________________GATGAGGTTGGGGATG CTCCATTCTTATCTTCATT C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165839648..165840170 26863196 MeRIP-seq:(Medium) rs1562762646 Functional Loss DEL dbSNP153 32..49 33 - - - 94775 RMVar_ID_94775 Human_SNP_ID_305275426 m1A Human chr6 - 165839941 165839933 165839941 TGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATGGAG TGAAGACAGAGATGTAGATGGGGATGGAAATGTGGTTGTAGATGGAGATGAGGTTGGGGATGGAG TCTTATCTT CTACAACCA PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165839631..165840115 26863196 MeRIP-seq:(Medium) rs796709268 Functional Loss MNV dbSNP153 33..41 33 - - - 94776 RMVar_ID_94776 Human_SNP_ID_305275441 m1A Human chr6 - 165839941 165839941 165839941 TGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATGGAG TGAAGACAGAGATGTAGATGGGGATGGAAATGTAGATAAGAATGGAGATGAGGTTGGGGATGGAG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165839631..165840115 26863196 MeRIP-seq:(Medium) rs1412170617 Functional Loss SNV dbSNP153 33..33 33 - - - 94777 RMVar_ID_94777 Human_SNP_ID_305275442 m1A Human chr6 - 165839941 165839941 165839941 TGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATGGAG TGAAGACAGAGATGTAGATGGGGATGGAAATGGAGATAAGAATGGAGATGAGGTTGGGGATGGAG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165839631..165840115 26863196 MeRIP-seq:(Medium) rs1412170617 Functional Loss SNV dbSNP153 33..33 33 - - - 94778 RMVar_ID_94778 Human_SNP_ID_305275443 m1A Human chr6 - 165839941 165839941 165839941 TGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATGGAG TGAAGACAGAGATGTAGATGGGGATGGAAATGCAGATAAGAATGGAGATGAGGTTGGGGATGGAG T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165839631..165840115 26863196 MeRIP-seq:(Medium) rs1412170617 Functional Loss SNV dbSNP153 33..33 33 - - - 94779 RMVar_ID_94779 Human_SNP_ID_305275444 m1A Human chr6 - 165839944 165839944 165839944 GGATGAAGACAGAGATGTAGATGGGGATGGAAATGAAGATAAGAATGGAGATGAGGTTGGGGATG GGATGAAGACAGAGATGTAGATGGGGATGGAATTGAAGATAAGAATGGAGATGAGGTTGGGGATG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165839648..165840170 26863196 MeRIP-seq:(Medium) rs1320989764 Functional Loss SNV dbSNP153 33..33 33 - - - 94780 RMVar_ID_94780 Human_SNP_ID_305275449 m1A Human chr6 + 165839949 165839949 165839949 CCAACCTCATCTCCATTCTTATCTTCATTTCCATCCCCATCTACATCTCTGTCTTCATCCCCATC CCAACCTCATCTCCATTCTTATCTTCATTTCCTTCCCCATCTACATCTCTGTCTTCATCCCCATC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165839592..165840191 26863196 MeRIP-seq:(Medium) rs1562762713 Functional Loss SNV dbSNP153 33..33 33 - - - 94781 RMVar_ID_94781 Human_SNP_ID_305287602 m1A Human chr6 - 165889833 165889833 165889833 GAGTGAGGGAGGAGTGAGGAGTGAGTGGGGCGAGAGGGAGGGAGGAGTAGGTGAGTGAGGAAATG GAGTGAGGGAGGAGTGAGGAGTGAGTGGGGCGTGAGGGAGGGAGGAGTAGGTGAGTGAGGAAATG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:165889701..165890225;chr6:165889565..165889909;chr6:165889612..165889932 26863196 MeRIP-seq:(Medium) rs1291612666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15728160 94782 RMVar_ID_94782 Human_SNP_ID_305287617 m1A Human chr6 + 165889851 165889851 165889851 CTCCTCCCTCCCTCTCGCCCCACTCACTCCTCACTCCTCCCTCACTCACTCCTCACTCCTCCCTC CTCCTCCCTCCCTCTCGCCCCACTCACTCCTCCCTCCTCCCTCACTCACTCCTCACTCCTCCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165889645..165889887 26863196 MeRIP-seq:(Medium) rs1215033182 Functional Loss SNV dbSNP153 33..33 33 - - - 94783 RMVar_ID_94783 Human_SNP_ID_305288462 m1A Human chr6 - 165892664 165892664 165892664 CAAAGGTGATGATGGGTCAGGGCCGGGGAGGGAGACACGGCCACTCACAGGGGACAGAGGAGCTG CAAAGGTGATGATGGGTCAGGGCCGGGGAGGGGGACACGGCCACTCACAGGGGACAGAGGAGCTG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165892614..165892753 26863196 MeRIP-seq:(Medium) rs1467550856 Functional Loss SNV dbSNP153 33..33 33 - - - 94784 RMVar_ID_94784 Human_SNP_ID_305289752 m1A Human chr6 - 165897442 165897442 165897442 CAGCTCAGGACCCTCTCATTCTCCTCCCTGGGACCCTCCCTATCTCCCCCACCCCCAAATACTGG CAGCTCAGGACCCTCTCATTCTCCTCCCTGGGGCCCTCCCTATCTCCCCCACCCCCAAATACTGG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165897401..165897555 26863196 MeRIP-seq:(Medium) rs1204821283 Functional Loss SNV dbSNP153 33..33 33 - - - 94785 RMVar_ID_94785 Human_SNP_ID_305291156 m1A Human chr6 + 165902661 165902661 165902661 AAGGAAGTTCTAGGAGGTGGCTACCCACCAGCAATGATATTTCCTCGCCATCCTTCCCATTCCAG AAGGAAGTTCTAGGAGGTGGCTACCCACCAGCGATGATATTTCCTCGCCATCCTTCCCATTCCAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165902476..165902825 26863196 MeRIP-seq:(Medium) rs921832885 Functional Loss SNV dbSNP153 33..33 33 - - - 94786 RMVar_ID_94786 Human_SNP_ID_305291176 m1A Human chr6 - 165902740 165902740 165902740 TGCCCTTCAGTCTTGGCCCAGAAACAATGCTGATACCTCCACTGACATTCCACTGGCAAGAACAG TGCCCTTCAGTCTTGGCCCAGAAACAATGCTGTTACCTCCACTGACATTCCACTGGCAAGAACAG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:165902501..165902782 26863196 MeRIP-seq:(Medium) rs978231211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15728325,Human_RBP_ID_27521078 94787 RMVar_ID_94787 Human_SNP_ID_305291408 m1A Human chr6 - 165903725 165903725 165903725 CAGCTTTTTTTTTGTATCTACACTTTCTCCCCAGGTGATCTCATCCAAAGTAATGGCTTTAATCA CAGCTTTTTTTTTGTATCTACACTTTCTCCCCGGGTGATCTCATCCAAAGTAATGGCTTTAATCA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165903701..165903725 26863196 MeRIP-seq:(Medium) rs1220012763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2991610,Human_RBP_ID_15728345,Human_RBP_ID_21390300 94788 RMVar_ID_94788 Human_SNP_ID_305291459 m1A Human chr6 - 165903939 165903939 165903939 ACTCCAGTGAAACTAACCTTGTTATGGTCCCCAGTGGCCTCCTTCTTGCTAAATCCATTGGCCAT ACTCCAGTGAAACTAACCTTGTTATGGTCCCCCGTGGCCTCCTTCTTGCTAAATCCATTGGCCAT T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165903926..165903950 26863196 MeRIP-seq:(Medium) rs1002155925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8636888,Human_RBP_ID_21220543 94789 RMVar_ID_94789 Human_SNP_ID_305292465 m1A Human chr6 + 165907268 165907268 165907268 GTGGTTGCAGGATTCACTGGTCCTGGTGGGAGATTCAGGATCCGGGCCATCACCACATCTCTTTC GTGGTTGCAGGATTCACTGGTCCTGGTGGGAGCTTCAGGATCCGGGCCATCACCACATCTCTTTC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165907226..165907375 26863196 MeRIP-seq:(Medium) rs529850542 Functional Loss SNV dbSNP153 33..33 33 - - - 94790 RMVar_ID_94790 Human_SNP_ID_305292493 m1A Human chr6 - 165907397 165907397 165907397 AGTTCCAGCAACGCGAGGCTCCCGGGAAGGGCAGCTGCTCTTTCAGAGGGAGGCTCTCGCCCACC AGTTCCAGCAACGCGAGGCTCCCGGGAAGGGCGGCTGCTCTTTCAGAGGGAGGCTCTCGCCCACC T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:165907330..165907532 32194978 MeRIP-seq:(Medium) rs1259530515 Functional Loss SNV dbSNP153 33..33 33 - - - 94791 RMVar_ID_94791 Human_SNP_ID_305298059 m1A Human chr6 + 165929216 165929212 165929216 TGGTAAAGACGTGGTTGGTGCAGAAAAACAAAAGAACTAAAACAAGATGCTTGTAAAGCACGCAG TGGTAAAGACGTGGTTGGTGCAGAAAAAC____GAACTAAAACAAGATGCTTGTAAAGCACGCAG CAAAA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165929205..165929345 26863196 MeRIP-seq:(Medium) rs1386583550 Functional Loss DEL dbSNP153 30..33 33 - - - 94792 RMVar_ID_94792 Human_SNP_ID_305298542 m1A Human chr6 - 165930924 165930924 165930924 GTTCTCCTTGCGGTTCCCTCAGTTTCATCAGCACCACGGTGGCTTCCCATGTTCCAGGCTGCGCC GTTCTCCTTGCGGTTCCCTCAGTTTCATCAGCGCCACGGTGGCTTCCCATGTTCCAGGCTGCGCC T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:165930776..165930992 26863196 MeRIP-seq:(Medium) rs1354961533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15932230 94793 RMVar_ID_94793 Human_SNP_ID_305300830 m1A Human chr6 + 165940386 165940386 165940386 GTACAGACGCGGGCAGCTACTTGCCAACAACCAGGCCGAGCATAAAGTAGTATCAAGGAAAATCA GTACAGACGCGGGCAGCTACTTGCCAACAACCGGGCCGAGCATAAAGTAGTATCAAGGAAAATCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165940335..165940418 26863196 MeRIP-seq:(Medium) rs1026907807 Functional Loss SNV dbSNP153 33..33 33 - - - 94794 RMVar_ID_94794 Human_SNP_ID_305300871 m1A Human chr6 - 165940534 165940534 165940534 AGTGTGAGCAGAAGCGGAGCCCGCAGAGCGCCAGGCTGCGCCGGGAGATGCATCACGATGAAAAA AGTGTGAGCAGAAGCGGAGCCCGCAGAGCGCCTGGCTGCGCCGGGAGATGCATCACGATGAAAAA T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165940487..165940744 26863196 MeRIP-seq:(Medium) rs1310808569 Functional Loss SNV dbSNP153 33..33 33 - - - 94795 RMVar_ID_94795 Human_SNP_ID_305301144 m1A Human chr6 + 165941695 165941695 165941695 GTGATGTGCCTGCTCTCCCTTTGCCTTCTGCCATGATTGTAAGCTTCCTGAGGCCTCCCTAAAAA GTGATGTGCCTGCTCTCCCTTTGCCTTCTGCCGTGATTGTAAGCTTCCTGAGGCCTCCCTAAAAA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165941644..165941825 26863196 MeRIP-seq:(Medium) rs1161060576 Functional Loss SNV dbSNP153 33..33 33 - - - 94796 RMVar_ID_94796 Human_SNP_ID_305301385 m1A Human chr6 - 165942581 165942581 165942581 AGGGCAGGTGAGCAGAGGCCCGAGAGCGGGGCAGAGCGGGGGCAGAGCGGCGAGCCCTGGCAAGC AGGGCAGGTGAGCAGAGGCCCGAGAGCGGGGCCGAGCGGGGGCAGAGCGGCGAGCCCTGGCAAGC T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165942546..165942637 26863196 MeRIP-seq:(Medium) rs1328092882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5621496 94797 RMVar_ID_94797 Human_SNP_ID_305303345 m1A Human chr6 - 165948623 165948623 165948623 CCTCGATGGTTTCTTGATGGGCCTCAGCTCTCAGCTACCTTCCTTAGCAGGAGTATTCGGGAACT CCTCGATGGTTTCTTGATGGGCCTCAGCTCTCGGCTACCTTCCTTAGCAGGAGTATTCGGGAACT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165948576..165948650 26863196 MeRIP-seq:(Medium) rs186428042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8637106,Human_RBP_ID_15729288 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94798 RMVar_ID_94798 Human_SNP_ID_305304058 m1A Human chr6 - 165951442 165951442 165951442 GGAGCTGTGGCAATCCAGCTGAAGGATGCTGGACACGGAAAGGAGGGCTGTTAGCCAATAGATCA GGAGCTGTGGCAATCCAGCTGAAGGATGCTGGGCACGGAAAGGAGGGCTGTTAGCCAATAGATCA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165951430..165951795 26863196 MeRIP-seq:(Medium) rs1017471120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5619608 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94799 RMVar_ID_94799 Human_SNP_ID_305304103 m1A Human chr6 + 165951551 165951551 165951551 CCTGAAGCAGAGCGACATCCAGCTTCTTCTGCACCACTCACGACGTAGGGTGAACTTCCAATGGG CCTGAAGCAGAGCGACATCCAGCTTCTTCTGCCCCACTCACGACGTAGGGTGAACTTCCAATGGG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165951501..165951710 26863196 MeRIP-seq:(Medium) rs987906012 Functional Loss SNV dbSNP153 33..33 33 - - - 94800 RMVar_ID_94800 Human_SNP_ID_305304128 m1A Human chr6 + 165951645 165951645 165951645 GGCTCCAGCCTTCCTTTCTCACTCGGTCTCCTAACACTGACTCCCCCATTTAGACGAGTCTGTTC GGCTCCAGCCTTCCTTTCTCACTCGGTCTCCTGACACTGACTCCCCCATTTAGACGAGTCTGTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165951470..165951796 26863196 MeRIP-seq:(Medium) rs1013020492 Functional Loss SNV dbSNP153 33..33 33 - - - 94801 RMVar_ID_94801 Human_SNP_ID_305307040 m1A Human chr6 + 165960973 165960973 165960973 AATGTGTCTTTGGGCAGAAGCAAGAGGGGAGGAAGCGTTGCCGGGGAGTGTGGCAGAACGCATAA AATGTGTCTTTGGGCAGAAGCAAGAGGGGAGGGAGCGTTGCCGGGGAGTGTGGCAGAACGCATAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:165960828..165961175 26863196 MeRIP-seq:(Medium) rs1236775494 Functional Loss SNV dbSNP153 33..33 33 - - - 94802 RMVar_ID_94802 Human_SNP_ID_305307085 m1A Human chr6 + 165961100 165961100 165961100 CCTCTCAGCCTGTCGATCTCCAGTCCGAGGCCAGGCTTGTGGTGGGAGGGTGGGGATGGGGTGCA CCTCTCAGCCTGTCGATCTCCAGTCCGAGGCCGGGCTTGTGGTGGGAGGGTGGGGATGGGGTGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165961076..165961100 26863196 MeRIP-seq:(Medium) rs968139387 Functional Loss SNV dbSNP153 33..33 33 - - - 94803 RMVar_ID_94803 Human_SNP_ID_305307761 m1A Human chr6 - 165963719 165963719 165963719 CAGCAAGAGGGGACTGATGGTGGGGTCAAGAGAGGAAGGAGTTGAGGCTTTTCTCAGGACAGGTG CAGCAAGAGGGGACTGATGGTGGGGTCAAGAGGGGAAGGAGTTGAGGCTTTTCTCAGGACAGGTG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165963699..165963900 26863196 MeRIP-seq:(Medium) rs1177025650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2993130,Human_RBP_ID_5618775 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94804 RMVar_ID_94804 Human_SNP_ID_305307784 m1A Human chr6 - 165963777 165963777 165963777 GAGGCACAGCACAGCCTGAGTGGTCAAGGAGGACGTGCCAGCAGGGGATACCACCTTCCAGCAAG GAGGCACAGCACAGCCTGAGTGGTCAAGGAGGGCGTGCCAGCAGGGGATACCACCTTCCAGCAAG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165963726..165963868 26863196 MeRIP-seq:(Medium) rs1360014728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2993131,Human_RBP_ID_21220965 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94805 RMVar_ID_94805 Human_SNP_ID_305307794 m1A Human chr6 - 165963816 165963815 165963817 GATAGAGGCCCAAGGAGGGATGGCCACAGCTCAGAGGAGGAGGCACAGCACAGCCTGAGTGGTCA GATAGAGGCCCAAGGAGGGATGGCCACAGCT__GAGGAGGAGGCACAGCACAGCCTGAGTGGTCA CTG C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165963801..165963825 26863196 MeRIP-seq:(Medium) rs1260431211 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94806 RMVar_ID_94806 Human_SNP_ID_305308953 m1A Human chr6 - 165968486 165968486 165968486 CCTCCTTGGTCAAAAGAAAATTAGCGTGTTGAAAATGTTTGGCCCATTTTCTAGAAATCTATGTA CCTCCTTGGTCAAAAGAAAATTAGCGTGTTGATAATGTTTGGCCCATTTTCTAGAAATCTATGTA T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165968480..165968606 26863196 MeRIP-seq:(Medium) rs1482625257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2993249,Human_RBP_ID_5621933,Human_RBP_ID_15729927 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94807 RMVar_ID_94807 Human_SNP_ID_305311015 m1A Human chr6 - 165976849 165976849 165976849 GAAGGTGGGGACAGGAGGATGGCATGGCGCACAGCCCGAGGAGGGCCCTGCTGCAGGGTGGCTGG GAAGGTGGGGACAGGAGGATGGCATGGCGCACCGCCCGAGGAGGGCCCTGCTGCAGGGTGGCTGG T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:165976798..165976909 26863196 MeRIP-seq:(Medium) rs1470586845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2993538,Human_RBP_ID_5621520,Human_RBP_ID_15730266 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94808 RMVar_ID_94808 Human_SNP_ID_305313276 m1A Human chr6 - 165986149 165986149 165986149 AGGAGGTGGCGGAGAACCCCAGCTCCCAGAGGAGGAACCCACTGCCTGGTTTGGGGACAGCAGCG AGGAGGTGGCGGAGAACCCCAGCTCCCAGAGGTGGAACCCACTGCCTGGTTTGGGGACAGCAGCG T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165986101..165986150 26863196 MeRIP-seq:(Medium) rs990327114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5619678 Human_Splice_Rec_832301,Human_Splice_Rec_832311,Human_Splice_Rec_832317 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94809 RMVar_ID_94809 Human_SNP_ID_305313330 m1A Human chr6 + 165986352 165986352 165986352 TGCAGAGGAAAGGGGTGGGGAGAAGAGACCAGAGAGGGAGATGGAAGAGATTGCTGCTTCAGGAG TGCAGAGGAAAGGGGTGGGGAGAAGAGACCAGGGAGGGAGATGGAAGAGATTGCTGCTTCAGGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165986340..165986472 26863196 MeRIP-seq:(Medium) rs1181888504 Functional Loss SNV dbSNP153 33..33 33 - - - 94810 RMVar_ID_94810 Human_SNP_ID_305313506 m1A Human chr6 + 165986792 165986792 165986792 GTTGGGCTTGGCTTGGCTTGGGGGGAGGGGGGACGGGACAGTGTTTGCAGTGTTTGGTGAGGATG GTTGGGCTTGGCTTGGCTTGGGGGGAGGGGGGGCGGGACAGTGTTTGCAGTGTTTGGTGAGGATG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165986776..165986800 26863196 MeRIP-seq:(Medium) rs956799363 Functional Loss SNV dbSNP153 33..33 33 - - - 94811 RMVar_ID_94811 Human_SNP_ID_305313631 m1A Human chr6 - 165987297 165987297 165987297 TGGACTCGAGAAAGAAGAAAAGGGAGTATATAAAGCCGAAGACTCAAGGGTTTGCAGAGGAGGGG TGGACTCGAGAAAGAAGAAAAGGGAGTATATACAGCCGAAGACTCAAGGGTTTGCAGAGGAGGGG T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:165987284..165987364 26863196 MeRIP-seq:(Medium) rs893832607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2993952,Human_RBP_ID_5617634,Human_RBP_ID_8637449,Human_RBP_ID_15730648,Human_RBP_ID_24147151,Human_RBP_ID_24511477 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94812 RMVar_ID_94812 Human_SNP_ID_305313649 m1A Human chr6 + 165987352 165987352 165987352 CTCGAGTCCACTCATCACCCTTTCCCCCAAACAGTCACCTCCACAAGCACAACACACCACACACG CTCGAGTCCACTCATCACCCTTTCCCCCAAACGGTCACCTCCACAAGCACAACACACCACACACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165987228..165987427 26863196 MeRIP-seq:(Medium) rs1031959375 Functional Loss SNV dbSNP153 33..33 33 - - - 94813 RMVar_ID_94813 Human_SNP_ID_305313817 m1A Human chr6 - 165987825 165987824 165987825 TTTCCCCGAGACCCCCAGATGGAAAGGAGGGAAGGAGGAACCCCACACACTCGCCTTTTGCGAGA TTTCCCCGAGACCCCCAGATGGAAAGGAGGGA_GGAGGAACCCCACACACTCGCCTTTTGCGAGA CT C PDE10A Ensembl:ENSG00000112541 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165987776..165987973 26863196 MeRIP-seq:(Medium) rs1382183314 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5622092,Human_RBP_ID_8637458 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 94814 RMVar_ID_94814 Human_SNP_ID_305313834 m1A Human chr6 + 165987863 165987863 165987863 CCTTTCCATCTGGGGGTCTCGGGGAAAGCTGCACCCAGCGCCTTGGGCGCCCATGAAGACCAGTC CCTTTCCATCTGGGGGTCTCGGGGAAAGCTGCGCCCAGCGCCTTGGGCGCCCATGAAGACCAGTC A G LINC00602 Ensembl:ENSG00000281832 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:165987815..165988141 26863196 MeRIP-seq:(Medium) rs915797772 Functional Loss SNV dbSNP153 33..33 33 - - - 94815 RMVar_ID_94815 Human_SNP_ID_305313864 m1A Human chr6 + 165987925 165987925 165987925 GTCCATCTCAGCTCAAGCTCCCAGCAGCAGCAACTTCGGACTCAGACCTCTCTCTTTAGAACATG GTCCATCTCAGCTCAAGCTCCCAGCAGCAGCAGCTTCGGACTCAGACCTCTCTCTTTAGAACATG A G LINC00602 Ensembl:ENSG00000281832 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165987876..165987925 26863196 MeRIP-seq:(Medium) rs1008409331 Functional Loss SNV dbSNP153 33..33 33 - - - 94816 RMVar_ID_94816 Human_SNP_ID_305409068 m1A Human chr6 - 166342517 166342517 166342517 CGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCAACAGAGTGGCGGCCGCTACGGCCCTGTAACAGG CGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCATCAGAGTGGCGGCCGCTACGGCCCTGTAACAGG T A SFT2D1 Ensembl:ENSG00000198818 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:166330245..166342600;chr6:166330230..166342600 26863196 MeRIP-seq:(Medium) rs533081754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252474,Human_RBP_ID_791243,Human_RBP_ID_4873013,Human_RBP_ID_5151999,Human_RBP_ID_5327266,Human_RBP_ID_8905922,Human_RBP_ID_9336377,Human_RBP_ID_18425531,Human_RBP_ID_22426618,Human_RBP_ID_22461529,Human_RBP_ID_24147313,Human_RBP_ID_27091586 Human_Splice_Rec_832437,Human_Splice_Rec_832451,Human_Splice_Rec_832467 94817 RMVar_ID_94817 Human_SNP_ID_305409069 m1A Human chr6 - 166342517 166342517 166342517 CGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCAACAGAGTGGCGGCCGCTACGGCCCTGTAACAGG CGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCAGCAGAGTGGCGGCCGCTACGGCCCTGTAACAGG T C SFT2D1 Ensembl:ENSG00000198818 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:166330245..166342600;chr6:166330230..166342600 26863196 MeRIP-seq:(Medium) rs533081754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252474,Human_RBP_ID_791243,Human_RBP_ID_4873013,Human_RBP_ID_5151999,Human_RBP_ID_5327266,Human_RBP_ID_8905922,Human_RBP_ID_9336377,Human_RBP_ID_18425531,Human_RBP_ID_22426618,Human_RBP_ID_22461529,Human_RBP_ID_24147313,Human_RBP_ID_27091586 Human_Splice_Rec_832437,Human_Splice_Rec_832451,Human_Splice_Rec_832467 94818 RMVar_ID_94818 Human_SNP_ID_305409070 m1A Human chr6 - 166342518 166342518 166342518 TCGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCAACAGAGTGGCGGCCGCTACGGCCCTGTAACAG TCGGGGTTTCCTGGTGGGCGTCAGGGGCAGGCCACAGAGTGGCGGCCGCTACGGCCCTGTAACAG T G SFT2D1 Ensembl:ENSG00000198818 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:166330201..166342600 26863196 MeRIP-seq:(Medium) rs1400312376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252474,Human_RBP_ID_791243,Human_RBP_ID_4873013,Human_RBP_ID_5151999,Human_RBP_ID_5327266,Human_RBP_ID_8905922,Human_RBP_ID_9336377,Human_RBP_ID_18425531,Human_RBP_ID_22426618,Human_RBP_ID_22461529,Human_RBP_ID_24147313,Human_RBP_ID_27091586 Human_Splice_Rec_832437,Human_Splice_Rec_832451,Human_Splice_Rec_832467 94819 RMVar_ID_94819 Human_SNP_ID_305415253 m1A Human chr6 + 166368822 166368822 166368822 TCCATAGTGATCTTCCTTTTCCTCCTTTTTTGACCAGGCCTTTCTCCACTTGGTCTATTTTCATC TCCATAGTGATCTTCCTTTTCCTCCTTTTTTGTCCAGGCCTTTCTCCACTTGGTCTATTTTCATC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:166368785..166368873 26863196 MeRIP-seq:(Medium) rs1481065919 Functional Loss SNV dbSNP153 33..33 33 - - - 94820 RMVar_ID_94820 Human_SNP_ID_305418572 m1A Human chr6 - 166382915 166382915 166382915 CCGGGGTGTCATTGGCTCTGGGAAGCGGCAGCAGAGGCAGGGACCACTCGGGGTCTGGTGTCGGC CCGGGGTGTCATTGGCTCTGGGAAGCGGCAGCGGAGGCAGGGACCACTCGGGGTCTGGTGTCGGC T C MPC1 Ensembl:ENSG00000060762 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:166382718..166382931 26863196 MeRIP-seq:(Medium) rs746906037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789628,Human_RBP_ID_4873030,Human_RBP_ID_9402964,Human_RBP_ID_22461530,Human_RBP_ID_27842520 RMVar_hsa_circ_91597,RMVar_hsa_circ_242960 94821 RMVar_ID_94821 Human_SNP_ID_305559664 m1A Human chr6 - 166931588 166931588 166931588 GTCTAGGTTTGCAGTTTCGGGACCGGTAGCTGAGGGGTCCCAGGGCCTTTCTTCTGTGAAGGAGA GTCTAGGTTTGCAGTTTCGGGACCGGTAGCTGGGGGGTCCCAGGGCCTTTCTTCTGTGAAGGAGA T C AL159163.1,RNASET2 Ensembl:ENSG00000249141,Ensembl:ENSG00000026297 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:166931586..166931712 26863196 MeRIP-seq:(Medium) rs1412477304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242978,RMVar_hsa_circ_375748,RMVar_hsa_circ_342127,RMVar_hsa_circ_242977 94822 RMVar_ID_94822 Human_SNP_ID_305566909 m1A Human chr6 + 166956151 166956151 166956151 CCAGGCAAAGCAACGCCAGGCAGAGGCAGCCCAGCAGGGCCCCGCGCAGGGCTGCAGGGCGCATG CCAGGCAAAGCAACGCCAGGCAGAGGCAGCCCGGCAGGGCCCCGCGCAGGGCTGCAGGGCGCATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:166956101..166956225 32194978 MeRIP-seq:(Medium) rs1330045184 Functional Loss SNV dbSNP153 33..33 33 - - - 94823 RMVar_ID_94823 Human_SNP_ID_305567025 m1A Human chr6 + 166956504 166956504 166956504 GCTTCGCGACCCACAGCGACCCCAGCTCCTCCACGCTGCAGCCGCCGTCCGCCCACGACCACGGT GCTTCGCGACCCACAGCGACCCCAGCTCCTCCGCGCTGCAGCCGCCGTCCGCCCACGACCACGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:166956193..166956595;chr6:166956159..166956554 26863196 MeRIP-seq:(Medium) rs2247325 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_541 94824 RMVar_ID_94824 Human_SNP_ID_305578160 m1A Human chr6 + 166999433 166999433 166999433 TGGAGAAGCAAGATGGCGGCGACGGCGGCCGCAGTGGTGGCCGAGGAGGACACGGAGCTGCGGGA TGGAGAAGCAAGATGGCGGCGACGGCGGCCGCGGTGGTGGCCGAGGAGGACACGGAGCTGCGGGA A G Z94721.2,FGFR1OP Ensembl:ENSG00000272980,Ensembl:ENSG00000213066 lincRNA,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:166999381..166999504 26863196 MeRIP-seq:(Medium) rs905499893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251861,Human_RBP_ID_657199,Human_RBP_ID_4904380,Human_RBP_ID_5401314,Human_RBP_ID_5620593,Human_RBP_ID_9336388,Human_RBP_ID_9402975,Human_RBP_ID_19019238,Human_RBP_ID_22105512,Human_RBP_ID_23067896,Human_RBP_ID_23120410,Human_RBP_ID_27828152 Human_Splice_Rec_833019,Human_Splice_Rec_833039,Human_Splice_Rec_833063,Human_Splice_Rec_833085,Human_Splice_Rec_833115 94825 RMVar_ID_94825 Human_SNP_ID_305584608 m1A Human chr6 - 167023080 167023080 167023080 GCAACTCCCTTACCTCCTCTAGCTCTTTGCTCACTGGGCACCTCCAAGTGAGGCCCCCTCCAATT GCAACTCCCTTACCTCCTCTAGCTCTTTGCTCTCTGGGCACCTCCAAGTGAGGCCCCCTCCAATT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:167023031..167023209 26863196 MeRIP-seq:(Medium) rs1387967741 Functional Loss SNV dbSNP153 33..33 33 - - - 94826 RMVar_ID_94826 Human_SNP_ID_305584609 m1A Human chr6 - 167023080 167023080 167023080 GCAACTCCCTTACCTCCTCTAGCTCTTTGCTCACTGGGCACCTCCAAGTGAGGCCCCCTCCAATT GCAACTCCCTTACCTCCTCTAGCTCTTTGCTCGCTGGGCACCTCCAAGTGAGGCCCCCTCCAATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:167023031..167023209 26863196 MeRIP-seq:(Medium) rs1387967741 Functional Loss SNV dbSNP153 33..33 33 - - - 94827 RMVar_ID_94827 Human_SNP_ID_305787247 m1A Human chr6 + 167826984 167826984 167826984 GACTGAGCCCCAGGCGGAGGCCAAGTCGGAGGACGCGGCGCGGCCGCGGAGGCGGAGGCAGCCGC GACTGAGCCCCAGGCGGAGGCCAAGTCGGAGGGCGCGGCGCGGCCGCGGAGGCGGAGGCAGCCGC A G AFDN Ensembl:ENSG00000130396 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr6:167826897..167827125;chr6:167826904..167826989 26863410 MeRIP-seq:(Medium) rs1377811327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903611,Human_RBP_ID_8905597,Human_RBP_ID_9336391,Human_RBP_ID_9437978,Human_RBP_ID_18195661,Human_RBP_ID_18425534,Human_RBP_ID_23067448 94828 RMVar_ID_94828 Human_SNP_ID_305787251 m1A Human chr6 + 167827007 167826990 167827008 AGTCGGAGGACGCGGCGCGGCCGCGGAGGCGGAGGCAGCCGCGGAGGCGGAGGCGGCCGGCGGGG AGTCGGAGGACGCGGC__________________GCAGCCGCGGAGGCGGAGGCGGCCGGCGGGG CGCGGCCGCGGAGGCGGAG C AFDN Ensembl:ENSG00000130396 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr6:167826876..167827177;chr6:167826930..167827120;chr6:167826894..167827219 26863196 MeRIP-seq:(Medium) rs1178549978 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_4873284,Human_RBP_ID_8905597,Human_RBP_ID_9336391,Human_RBP_ID_18425534,Human_RBP_ID_23067448,Human_RBP_ID_27828153 RMVar_hsa_circ_97075,RMVar_hsa_circ_243002 94829 RMVar_ID_94829 Human_SNP_ID_305787258 m1A Human chr6 + 167827011 167826993 167827011 GGAGGACGCGGCGCGGCCGCGGAGGCGGAGGCAGCCGCGGAGGCGGAGGCGGCCGGCGGGGGGTG GGAGGACGCGGCGCG__________________GCCGCGGAGGCGGAGGCGGCCGGCGGGGGGTG GGCCGCGGAGGCGGAGGCA G AFDN Ensembl:ENSG00000130396 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:167826909..167827193 26863196 MeRIP-seq:(Medium) rs1280947509 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_4903611,Human_RBP_ID_8905597,Human_RBP_ID_9336391,Human_RBP_ID_18425793,Human_RBP_ID_23067448,Human_RBP_ID_27828153 RMVar_hsa_circ_97075,RMVar_hsa_circ_243002 94830 RMVar_ID_94830 Human_SNP_ID_305787271 m1A Human chr6 + 167827011 167827011 167827011 GGAGGACGCGGCGCGGCCGCGGAGGCGGAGGCAGCCGCGGAGGCGGAGGCGGCCGGCGGGGGGTG GGAGGACGCGGCGCGGCCGCGGAGGCGGAGGCGGCCGCGGAGGCGGAGGCGGCCGGCGGGGGGTG A G AFDN Ensembl:ENSG00000130396 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:167826909..167827193 26863196 MeRIP-seq:(Medium) rs1364775649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903611,Human_RBP_ID_8905597,Human_RBP_ID_9336391,Human_RBP_ID_18425793,Human_RBP_ID_23067448,Human_RBP_ID_27828153 RMVar_hsa_circ_97075,RMVar_hsa_circ_243002 94831 RMVar_ID_94831 Human_SNP_ID_305787340 m1A Human chr6 + 167827114 167827112 167827115 GCCCGTCCTCCGGCCCCGGCCCCGCGCGGCTGAGGAGGCGCGGCCAGGACCATGTCGGCGGGCGG GCCCGTCCTCCGGCCCCGGCCCCGCGCGGCT___GAGGCGCGGCCAGGACCATGTCGGCGGGCGG TGAG T AFDN Ensembl:ENSG00000130396 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:167826900..167827189 26863196 MeRIP-seq:(Medium) rs887205321 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4903611,Human_RBP_ID_5242746,Human_RBP_ID_8905597,Human_RBP_ID_9336392,Human_RBP_ID_23067899,Human_RBP_ID_27091985,Human_RBP_ID_27829073 RMVar_hsa_circ_97075,RMVar_hsa_circ_243002 94832 RMVar_ID_94832 Human_SNP_ID_305787341 m1A Human chr6 - 167827112 167827112 167827112 GCCCGCCGACATGGTCCTGGCCGCGCCTCCTCAGCCGCGCGGGGCCGGGGCCGGAGGACGGGCCG GCCCGCCGACATGGTCCTGGCCGCGCCTCCTCGGCCGCGCGGGGCCGGGGCCGGAGGACGGGCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:167826972..167827129 26863196 MeRIP-seq:(Medium) rs1389360931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243003 94833 RMVar_ID_94833 Human_SNP_ID_305819251 m1A Human chr6 + 167952159 167952159 167952159 GGACGATGATGTGGACACCATGCTGATCATGCAGCGCCTGGAGGCTGAACGAAGAGCGAGGGTAA GGACGATGATGTGGACACCATGCTGATCATGCGGCGCCTGGAGGCTGAACGAAGAGCGAGGGTAA A G AFDN Ensembl:ENSG00000130396 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:167952114..167952194 26863196 MeRIP-seq:(Medium) rs771508660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251517,Human_RBP_ID_950916,Human_RBP_ID_3970627,Human_RBP_ID_9309895,Human_RBP_ID_9401433,Human_RBP_ID_18171139,Human_RBP_ID_22830030,Human_RBP_ID_23067454,Human_RBP_ID_24548661,Human_RBP_ID_24554680,Human_RBP_ID_26354613,Human_RBP_ID_27828181 Human_Splice_Rec_833529,Human_Splice_Rec_833589,Human_Splice_Rec_833651,Human_Splice_Rec_833705,Human_Splice_Rec_833827,Human_Splice_Rec_833889,Human_Splice_Rec_833953,Human_Splice_Rec_834005,Human_Splice_Rec_834025,Human_Splice_Rec_834033 RMVar_hsa_circ_18189,RMVar_hsa_circ_91897,RMVar_hsa_circ_243011,RMVar_hsa_circ_112581,RMVar_hsa_circ_49754,RMVar_hsa_circ_243024,RMVar_hsa_circ_92159,RMVar_hsa_circ_243036,RMVar_hsa_circ_268899,RMVar_hsa_circ_76045,RMVar_hsa_circ_243039,RMVar_hsa_circ_92017,RMVar_hsa_circ_90633,RMVar_hsa_circ_243045,RMVar_hsa_circ_111983,RMVar_hsa_circ_243046,RMVar_hsa_circ_269387,RMVar_hsa_circ_377050,RMVar_hsa_circ_243047,RMVar_hsa_circ_378462,RMVar_hsa_circ_41725,RMVar_hsa_circ_63448,RMVar_hsa_circ_337853,RMVar_hsa_circ_350024,RMVar_hsa_circ_95895,RMVar_hsa_circ_267993,RMVar_hsa_circ_366256,RMVar_hsa_circ_73122,RMVar_hsa_circ_49246,RMVar_hsa_circ_243049 94834 RMVar_ID_94834 Human_SNP_ID_305821879 m1A Human chr6 + 167962489 167962489 167962489 CAGCAGCAGTTAGAAGAGATGCGCAAGCGGGAAGCGGAAGACCGAGCGAGGCAAGAGGAAGAGCG CAGCAGCAGTTAGAAGAGATGCGCAAGCGGGAGGCGGAAGACCGAGCGAGGCAAGAGGAAGAGCG A G AFDN Ensembl:ENSG00000130396 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:167962385..167962596 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_251518,Human_RBP_ID_841300,Human_RBP_ID_950917,Human_RBP_ID_3969473,Human_RBP_ID_8944050,Human_RBP_ID_9403033,Human_RBP_ID_24548516,Human_RBP_ID_26354615,Human_RBP_ID_27828182 Human_Splice_Rec_833532,Human_Splice_Rec_833590,Human_Splice_Rec_833591,Human_Splice_Rec_833652,Human_Splice_Rec_833706,Human_Splice_Rec_833707,Human_Splice_Rec_833828,Human_Splice_Rec_833829,Human_Splice_Rec_833892,Human_Splice_Rec_833893,Human_Splice_Rec_833954,Human_Splice_Rec_833955,Human_Splice_Rec_834006,Human_Splice_Rec_834026,Human_Splice_Rec_834027,Human_Splice_Rec_834034 RMVar_hsa_circ_91897,RMVar_hsa_circ_243011,RMVar_hsa_circ_112581,RMVar_hsa_circ_49754,RMVar_hsa_circ_243024,RMVar_hsa_circ_92159,RMVar_hsa_circ_243036,RMVar_hsa_circ_76045,RMVar_hsa_circ_243039,RMVar_hsa_circ_92017,RMVar_hsa_circ_90633,RMVar_hsa_circ_243045,RMVar_hsa_circ_111983,RMVar_hsa_circ_243046,RMVar_hsa_circ_269387,RMVar_hsa_circ_377050,RMVar_hsa_circ_243047,RMVar_hsa_circ_63448,RMVar_hsa_circ_350024,RMVar_hsa_circ_95895,RMVar_hsa_circ_366256,RMVar_hsa_circ_73122,RMVar_hsa_circ_243049 94835 RMVar_ID_94835 Human_SNP_ID_305821880 m1A Human chr6 + 167962489 167962489 167962489 CAGCAGCAGTTAGAAGAGATGCGCAAGCGGGAAGCGGAAGACCGAGCGAGGCAAGAGGAAGAGCG CAGCAGCAGTTAGAAGAGATGCGCAAGCGGGATGCGGAAGACCGAGCGAGGCAAGAGGAAGAGCG A T AFDN Ensembl:ENSG00000130396 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:167962385..167962596 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_251518,Human_RBP_ID_841300,Human_RBP_ID_950917,Human_RBP_ID_3969473,Human_RBP_ID_8944050,Human_RBP_ID_9403033,Human_RBP_ID_24548516,Human_RBP_ID_26354615,Human_RBP_ID_27828182 Human_Splice_Rec_833532,Human_Splice_Rec_833590,Human_Splice_Rec_833591,Human_Splice_Rec_833652,Human_Splice_Rec_833706,Human_Splice_Rec_833707,Human_Splice_Rec_833828,Human_Splice_Rec_833829,Human_Splice_Rec_833892,Human_Splice_Rec_833893,Human_Splice_Rec_833954,Human_Splice_Rec_833955,Human_Splice_Rec_834006,Human_Splice_Rec_834026,Human_Splice_Rec_834027,Human_Splice_Rec_834034 RMVar_hsa_circ_91897,RMVar_hsa_circ_243011,RMVar_hsa_circ_112581,RMVar_hsa_circ_49754,RMVar_hsa_circ_243024,RMVar_hsa_circ_92159,RMVar_hsa_circ_243036,RMVar_hsa_circ_76045,RMVar_hsa_circ_243039,RMVar_hsa_circ_92017,RMVar_hsa_circ_90633,RMVar_hsa_circ_243045,RMVar_hsa_circ_111983,RMVar_hsa_circ_243046,RMVar_hsa_circ_269387,RMVar_hsa_circ_377050,RMVar_hsa_circ_243047,RMVar_hsa_circ_63448,RMVar_hsa_circ_350024,RMVar_hsa_circ_95895,RMVar_hsa_circ_366256,RMVar_hsa_circ_73122,RMVar_hsa_circ_243049 94836 RMVar_ID_94836 Human_SNP_ID_305822696 m1A Human chr6 - 167965713 167965713 167965713 AATAGACAAGAGTGCAAAGGTCAGAGGTGAGAAGGGAACAGCCGACCCACTGGGCCTTCAAAGGG AATAGACAAGAGTGCAAAGGTCAGAGGTGAGAGGGGAACAGCCGACCCACTGGGCCTTCAAAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:167965709..167965879 26863196 MeRIP-seq:(Medium) rs759473271 Functional Loss SNV dbSNP153 33..33 33 - - - 94837 RMVar_ID_94837 Human_SNP_ID_305822788 m1A Human chr6 - 167965859 167965859 167965859 GGGCTCGTAGTCCCGGGGAAGCGGAGGGCGGCACAGACCGGGCGCCTCGGGCTCCAGCAACCTGC GGGCTCGTAGTCCCGGGGAAGCGGAGGGCGGCCCAGACCGGGCGCCTCGGGCTCCAGCAACCTGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:167965823..167965949 26863196 MeRIP-seq:(Medium) rs754308498 Functional Loss SNV dbSNP153 33..33 33 - - - 94838 RMVar_ID_94838 Human_SNP_ID_305822820 m1A Human chr6 - 167965901 167965901 167965901 AGGCGGGGGAGGAGGGGCGCCGGGCGCGGGGGACGGGGACGGGGGCTCGTAGTCCCGGGGAAGCG AGGCGGGGGAGGAGGGGCGCCGGGCGCGGGGGTCGGGGACGGGGGCTCGTAGTCCCGGGGAAGCG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:167965776..167966025 26863410 MeRIP-seq:(Medium) rs1409446539 Functional Loss SNV dbSNP153 33..33 33 - - - 94839 RMVar_ID_94839 Human_SNP_ID_305924860 m1A Human chr6 + 168319630 168319630 168319630 GCCCGCGGACCCCGGGGGTCCGCCCGGCGTCCACATCTCCCGGGCAGGGTCCCGGCCTCCCGAAC GCCCGCGGACCCCGGGGGTCCGCCCGGCGTCCGCATCTCCCGGGCAGGGTCCCGGCCTCCCGAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:168319499..168319833 26863196 MeRIP-seq:(Medium) rs1254898035 Functional Loss SNV dbSNP153 33..33 33 - - - 94840 RMVar_ID_94840 Human_SNP_ID_306169551 m1A Human chr6 - 169221500 169221500 169221500 CTCAGGTGCGAACCTTATGGCACGACCCCAGGAACATTGGCTGGAAGGACTACACGGCCTATAGG CTCAGGTGCGAACCTTATGGCACGACCCCAGGCACATTGGCTGGAAGGACTACACGGCCTATAGG T G THBS2 Ensembl:ENSG00000186340 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:169221451..169221550 32194978 MeRIP-seq:(Medium) rs1212274901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_834626,Human_Splice_Rec_834627,Human_Splice_Rec_834668,Human_Splice_Rec_834669,Human_Splice_Rec_834710,Human_Splice_Rec_834711,Human_Splice_Rec_834718,Human_Splice_Rec_834719 RMVar_hsa_circ_114016,RMVar_hsa_circ_121175,RMVar_hsa_circ_243062,RMVar_hsa_circ_112051,RMVar_hsa_circ_124008,RMVar_hsa_circ_302240,RMVar_hsa_circ_89719,RMVar_hsa_circ_243064,RMVar_hsa_circ_243066,RMVar_hsa_circ_88270,RMVar_hsa_circ_243067,RMVar_hsa_circ_243065,RMVar_hsa_circ_243063,RMVar_hsa_circ_243069 94841 RMVar_ID_94841 Human_SNP_ID_306170704 m1A Human chr6 - 169225351 169225351 169225351 CTAGACCGACGTGGACAATGACCTTGTTGGGGACCAGTGTGACAACAACGAGGACATAGATGACG CTAGACCGACGTGGACAATGACCTTGTTGGGGCCCAGTGTGACAACAACGAGGACATAGATGACG T G THBS2 Ensembl:ENSG00000186340 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:169225326..169225350 32194978 MeRIP-seq:(Medium) rs1280481974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_834620,Human_Splice_Rec_834662,Human_Splice_Rec_834704 RMVar_hsa_circ_114016,RMVar_hsa_circ_121175,RMVar_hsa_circ_243062,RMVar_hsa_circ_112051,RMVar_hsa_circ_124008,RMVar_hsa_circ_89719,RMVar_hsa_circ_243064,RMVar_hsa_circ_243066,RMVar_hsa_circ_88270,RMVar_hsa_circ_243065,RMVar_hsa_circ_243063,RMVar_hsa_circ_33893,RMVar_hsa_circ_114333,RMVar_hsa_circ_124355,RMVar_hsa_circ_243069,RMVar_hsa_circ_107639,RMVar_hsa_circ_83223,RMVar_hsa_circ_243071,RMVar_hsa_circ_243072,RMVar_hsa_circ_243070,RMVar_hsa_circ_243073 94842 RMVar_ID_94842 Human_SNP_ID_306279811 m1A Human chr6 - 169649873 169649873 169649873 AGGGGATGGAGGGATGGAGAGATGAGATATGGATGAGTGGCTCAATTGATGGGGGGGATGGATGG AGGGGATGGAGGGATGGAGAGATGAGATATGGTTGAGTGGCTCAATTGATGGGGGGGATGGATGG T A WDR27,AL031315.1 Ensembl:ENSG00000184465,Ensembl:ENSG00000285733 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:169649824..169649919 26863196 MeRIP-seq:(Medium) rs568092986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821461,Human_RBP_ID_5401329,Human_RBP_ID_5656628,Human_RBP_ID_8215446,Human_RBP_ID_17310470,Human_RBP_ID_21991019,Human_RBP_ID_22617711,Human_RBP_ID_24148928 RMVar_hsa_circ_370265,RMVar_hsa_circ_311533,RMVar_hsa_circ_312825,RMVar_hsa_circ_280668,RMVar_hsa_circ_290644,RMVar_hsa_circ_283452,RMVar_hsa_circ_127253,RMVar_hsa_circ_265902,RMVar_hsa_circ_9960,RMVar_hsa_circ_243087,RMVar_hsa_circ_243088,RMVar_hsa_circ_243085,RMVar_hsa_circ_243086,RMVar_hsa_circ_243084,RMVar_hsa_circ_375969,RMVar_hsa_circ_289539,RMVar_hsa_circ_8467,RMVar_hsa_circ_20825,RMVar_hsa_circ_243097,RMVar_hsa_circ_243098,RMVar_hsa_circ_292575,RMVar_hsa_circ_284246,RMVar_hsa_circ_370420,RMVar_hsa_circ_296397,RMVar_hsa_circ_276659,RMVar_hsa_circ_17272,RMVar_hsa_circ_109,RMVar_hsa_circ_23007,RMVar_hsa_circ_243101,RMVar_hsa_circ_243103,RMVar_hsa_circ_243102,RMVar_hsa_circ_126062,RMVar_hsa_circ_243105,RMVar_hsa_circ_378025,RMVar_hsa_circ_243107,RMVar_hsa_circ_243106,RMVar_hsa_circ_57434,RMVar_hsa_circ_292009,RMVar_hsa_circ_300908,RMVar_hsa_circ_316843,RMVar_hsa_circ_118014,RMVar_hsa_circ_120664,RMVar_hsa_circ_328895,RMVar_hsa_circ_13792,RMVar_hsa_circ_243109,RMVar_hsa_circ_243110,RMVar_hsa_circ_243108 94843 RMVar_ID_94843 Human_SNP_ID_306285723 m1A Human chr6 - 169668443 169668443 169668443 GAACAGATGCTGAGGGATTGGGAAGGCAGAGCAGTACATTCTGAGTTACAGGCGGGGAGCCTCAG GAACAGATGCTGAGGGATTGGGAAGGCAGAGCGGTACATTCTGAGTTACAGGCGGGGAGCCTCAG T C WDR27,AL031315.1 Ensembl:ENSG00000184465,Ensembl:ENSG00000285733 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:169668394..169668552 26863196 MeRIP-seq:(Medium) rs905550895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7575761,Human_RBP_ID_15741562,Human_RBP_ID_23057947,Human_RBP_ID_25986360 RMVar_hsa_circ_50898,RMVar_hsa_circ_290644,RMVar_hsa_circ_127253,RMVar_hsa_circ_265902,RMVar_hsa_circ_243084,RMVar_hsa_circ_20825,RMVar_hsa_circ_296397,RMVar_hsa_circ_13792,RMVar_hsa_circ_355096,RMVar_hsa_circ_268612,RMVar_hsa_circ_116483,RMVar_hsa_circ_243111,RMVar_hsa_circ_6313,RMVar_hsa_circ_58669,RMVar_hsa_circ_51561,RMVar_hsa_circ_67185,RMVar_hsa_circ_12106,RMVar_hsa_circ_243118,RMVar_hsa_circ_291220,RMVar_hsa_circ_353965,RMVar_hsa_circ_322395 94844 RMVar_ID_94844 Human_SNP_ID_306286508 m1A Human chr6 + 169671612 169671612 169671612 TGAGACTCTCCTAACATCAGCATGCTCCAAGCACACAGGCAGGTTCTCACTCTTCCCAGGGCCTT TGAGACTCTCCTAACATCAGCATGCTCCAAGCGCACAGGCAGGTTCTCACTCTTCCCAGGGCCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:169671561..169671803 26863196 MeRIP-seq:(Medium) rs1177316872 Functional Loss SNV dbSNP153 33..33 33 - - - 94845 RMVar_ID_94845 Human_SNP_ID_306294164 m1A Human chr6 - 169701745 169701745 169701745 GCGATTTGAGGGTTCCGCCGTGACCGCTTCCAACGGCGGACACGCGCGCTCTGGACCAGAGCCGT GCGATTTGAGGGTTCCGCCGTGACCGCTTCCAGCGGCGGACACGCGCGCTCTGGACCAGAGCCGT T C WDR27,AL031315.1 Ensembl:ENSG00000184465,Ensembl:ENSG00000285733 Protein coding,Protein coding 5'UTR,5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1137523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5532999,Human_RBP_ID_9403055,Human_RBP_ID_17163933 GWAS_ID_12469 RMVar_hsa_circ_116483,RMVar_hsa_circ_243111 94846 RMVar_ID_94846 Human_SNP_ID_306300695 m1A Human chr6 - 169723965 169723956 169723965 GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTCGGGCT GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG_________GCGGCGGCGCGGGGCGCTCGGGCT CCGCCGCCGT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:169723820..169724025;chr6:169721001..169724025;chr6:169723782..169724025 26863196 MeRIP-seq:(Medium) rs1277497350 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94847 RMVar_ID_94847 Human_SNP_ID_306300699 m1A Human chr6 - 169723965 169723959 169723965 GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTCGGGCT GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG______GCGGCGGCGGCGCGGGGCGCTCGGGCT CCGCCGT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:169723820..169724025;chr6:169721001..169724025;chr6:169723782..169724025 26863196 MeRIP-seq:(Medium) rs1332368284 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94848 RMVar_ID_94848 Human_SNP_ID_306300704 m1A Human chr6 - 169723965 169723962 169723965 GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTCGGGCT GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG___GCGGCGGCGGCGGCGCGGGGCGCTCGGGCT CCGT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:169723820..169724025;chr6:169721001..169724025;chr6:169723782..169724025 26863196 MeRIP-seq:(Medium) rs948194639 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94849 RMVar_ID_94849 Human_SNP_ID_306300706 m1A Human chr6 - 169723970 169723965 169723971 CGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTC CGGCAGCGGCGGCGGCGGCCGGGACAAGGCG______ACGGCGGCGGCGGCGGCGCGGGGCGCTC TCGCCTC T PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:169723869..169725466 26863410 MeRIP-seq:(Medium) rs982241960 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8237649,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94850 RMVar_ID_94850 Human_SNP_ID_306300707 m1A Human chr6 - 169723965 169723965 169723965 GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTCGGGCT GCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGGCGGCGGCGGCGGCGGCGCGGGGCGCTCGGGCT T C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:169723820..169724025;chr6:169721001..169724025;chr6:169723782..169724025 26863196 MeRIP-seq:(Medium) rs1444168698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94851 RMVar_ID_94851 Human_SNP_ID_306300711 m1A Human chr6 - 169723970 169723970 169723970 CGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTC CGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGTGGCGACGGCGGCGGCGGCGGCGCGGGGCGCTC T A PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:169723869..169725466 26863410 MeRIP-seq:(Medium) rs1355319142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821473,Human_RBP_ID_4904385,Human_RBP_ID_5217198,Human_RBP_ID_8237649,Human_RBP_ID_8730341,Human_RBP_ID_9309463,Human_RBP_ID_22728272 94852 RMVar_ID_94852 Human_SNP_ID_306300715 m1A Human chr6 - 169723998 169723983 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGC_______________CGGGACAAGGCGGAGGCG GGCCGCCGCCGCCGCT G PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs1309845535 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94853 RMVar_ID_94853 Human_SNP_ID_306300731 m1A Human chr6 - 169723998 169723986 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGC____________GGCCGGGACAAGGCGGAGGCG CGCCGCCGCCGCT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs1452658447 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94854 RMVar_ID_94854 Human_SNP_ID_306300732 m1A Human chr6 - 169723998 169723989 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGC_________GGCGGCCGGGACAAGGCGGAGGCG CGCCGCCGCT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs1416301203 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94855 RMVar_ID_94855 Human_SNP_ID_306300737 m1A Human chr6 - 169723998 169723992 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGC______GGCGGCGGCCGGGACAAGGCGGAGGCG CGCCGCT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs1201836642 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94856 RMVar_ID_94856 Human_SNP_ID_306300741 m1A Human chr6 - 169723998 169723995 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGC___GGCGGCGGCGGCCGGGACAAGGCGGAGGCG CGCT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs1298404111 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94857 RMVar_ID_94857 Human_SNP_ID_306300743 m1A Human chr6 - 169723998 169723998 169723998 GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG GCCCGCGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCCGGGACAAGGCGGAGGCG T C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:169723901..169725466 26863410 MeRIP-seq:(Medium) rs866592785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252195,Human_RBP_ID_3821473,Human_RBP_ID_4903617,Human_RBP_ID_5217260,Human_RBP_ID_5242748,Human_RBP_ID_5327280,Human_RBP_ID_8215458,Human_RBP_ID_8237570,Human_RBP_ID_8730342,Human_RBP_ID_9336843,Human_RBP_ID_9437708,Human_RBP_ID_18957861,Human_RBP_ID_21991026,Human_RBP_ID_22619570,Human_RBP_ID_22728273,Human_RBP_ID_26793414 94858 RMVar_ID_94858 Human_SNP_ID_306300924 m1A Human chr6 - 169724359 169724355 169724359 GGGCTGAGGCGGCCGCGGGGCTGAGGCGAGCGAGCGGCGGGGCTGAGGCGAGCGAGTGGCGGGGC GGGCTGAGGCGGCCGCGGGGCTGAGGCGAGCG____GCGGGGCTGAGGCGAGCGAGTGGCGGGGC CCGCT C PHF10 Ensembl:ENSG00000130024 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:169724093..169724500 26863196 MeRIP-seq:(Medium) rs1336722453 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3821035,Human_RBP_ID_3969483,Human_RBP_ID_4903618,Human_RBP_ID_5217263,Human_RBP_ID_5327283,Human_RBP_ID_5510881,Human_RBP_ID_8143875,Human_RBP_ID_8215460,Human_RBP_ID_8237170,Human_RBP_ID_8730343,Human_RBP_ID_8905930,Human_RBP_ID_8944052,Human_RBP_ID_9336401,Human_RBP_ID_9354666,Human_RBP_ID_9437711,Human_RBP_ID_17069879,Human_RBP_ID_17161790,Human_RBP_ID_17663541,Human_RBP_ID_18425540,Human_RBP_ID_18465880,Human_RBP_ID_18957863,Human_RBP_ID_21991028,Human_RBP_ID_22461554,Human_RBP_ID_22703152,Human_RBP_ID_22728275,Human_RBP_ID_24149340,Human_RBP_ID_24386957,Human_RBP_ID_24554682,Human_RBP_ID_26354630,Human_RBP_ID_26792660,Human_RBP_ID_27828189,Human_RBP_ID_27842536 94859 RMVar_ID_94859 Human_SNP_ID_306300977 m1A Human chr6 + 169724441 169724441 169724441 CCGCCGCTCGCCTCAGCCCCGCCGCTCCCCTCAGCCCCGCGGCCGCCTCAGCCCCGCCGCCGCCT CCGCCGCTCGCCTCAGCCCCGCCGCTCCCCTCCGCCCCGCGGCCGCCTCAGCCCCGCCGCCGCCT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chr6:169724283..169724481;chr6:169724370..169724478 26863196,26863410 MeRIP-seq:(Medium) rs1285311521 Functional Loss SNV dbSNP153 33..33 33 - - - 94860 RMVar_ID_94860 Human_SNP_ID_306300978 m1A Human chr6 + 169724441 169724441 169724441 CCGCCGCTCGCCTCAGCCCCGCCGCTCCCCTCAGCCCCGCGGCCGCCTCAGCCCCGCCGCCGCCT CCGCCGCTCGCCTCAGCCCCGCCGCTCCCCTCGGCCCCGCGGCCGCCTCAGCCCCGCCGCCGCCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chr6:169724283..169724481;chr6:169724370..169724478 26863196,26863410 MeRIP-seq:(Medium) rs1285311521 Functional Loss SNV dbSNP153 33..33 33 - - - 94861 RMVar_ID_94861 Human_SNP_ID_306307264 m1A Human chr6 - 169751377 169751377 169751377 ACCAGACCCCTCAGCAGGCTCCGGTGACGCCTAGGAAAGAAAGGAGGCCTAGCATGTTCGAGAAG ACCAGACCCCTCAGCAGGCTCCGGTGACGCCTGGGAAAGAAAGGAGGCCTAGCATGTTCGAGAAG T C TCTE3 Ensembl:ENSG00000184786 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:169751330..169751538 26863196 MeRIP-seq:(Medium) rs141108786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_835301 94862 RMVar_ID_94862 Human_SNP_ID_306307265 m1A Human chr6 - 169751377 169751377 169751377 ACCAGACCCCTCAGCAGGCTCCGGTGACGCCTAGGAAAGAAAGGAGGCCTAGCATGTTCGAGAAG ACCAGACCCCTCAGCAGGCTCCGGTGACGCCTCGGAAAGAAAGGAGGCCTAGCATGTTCGAGAAG T G TCTE3 Ensembl:ENSG00000184786 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:169751330..169751538 26863196 MeRIP-seq:(Medium) rs141108786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_835301 94863 RMVar_ID_94863 Human_SNP_ID_306424285 m1A Human chr6 + 170177361 170177361 170177361 GCGGGGGAGGGGCAGTCGGCGGGGGGAGGGGCAGTCGGCGGGGGGAGGGGCAGCCGGTCGGGAGG GCGGGGGAGGGGCAGTCGGCGGGGGGAGGGGCCGTCGGCGGGGGGAGGGGCAGCCGGTCGGGAGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:170177333..170177462 26863196 MeRIP-seq:(Medium) rs1381739635 Functional Loss SNV dbSNP153 33..33 33 - - - 94864 RMVar_ID_94864 Human_SNP_ID_306464204 m1A Human chr6 + 170317447 170317447 170317447 TTTGTGGGAAGTACCTGCCCACATATATGTACAGTAGTAAATTTCAAAGAACTGGCAGAGCACCA TTTGTGGGAAGTACCTGCCCACATATATGTACGGTAGTAAATTTCAAAGAACTGGCAGAGCACCA A G FAM120B Ensembl:ENSG00000112584 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:170317344..170317461 26863196 MeRIP-seq:(Medium) rs1020720237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2014967,Human_RBP_ID_4905652,Human_RBP_ID_9401449,Human_RBP_ID_15743291,Human_RBP_ID_18859170,Human_RBP_ID_21902640,Human_RBP_ID_24149452,Human_RBP_ID_27092520 Human_Splice_Rec_835634,Human_Splice_Rec_835654,Human_Splice_Rec_835674 Human_miRNA_ID_2729359,Human_miRNA_ID_2729360 RMVar_hsa_circ_114410,RMVar_hsa_circ_292584,RMVar_hsa_circ_116294,RMVar_hsa_circ_243139,RMVar_hsa_circ_319382,RMVar_hsa_circ_283417,RMVar_hsa_circ_289213,RMVar_hsa_circ_273880,RMVar_hsa_circ_243141,RMVar_hsa_circ_243143,RMVar_hsa_circ_243145,RMVar_hsa_circ_243146,RMVar_hsa_circ_243144,RMVar_hsa_circ_243142,RMVar_hsa_circ_243140 94865 RMVar_ID_94865 Human_SNP_ID_306464660 m1A Human chr6 + 170318567 170318567 170318567 ACCCTGAACCCAGGCAAGAAGTTCCCACGTGTACAGGCCCTGAATCCAGGCGAGAAGTTCCCATG ACCCTGAACCCAGGCAAGAAGTTCCCACGTGTTCAGGCCCTGAATCCAGGCGAGAAGTTCCCATG A T FAM120B Ensembl:ENSG00000112584 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:170318520..170318665 26863196 MeRIP-seq:(Medium) rs878927734 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4873927,Human_RBP_ID_21903485,Human_RBP_ID_26354633 RMVar_hsa_circ_114410,RMVar_hsa_circ_292584,RMVar_hsa_circ_116294,RMVar_hsa_circ_243139,RMVar_hsa_circ_319382,RMVar_hsa_circ_283417,RMVar_hsa_circ_289213,RMVar_hsa_circ_273880,RMVar_hsa_circ_243141,RMVar_hsa_circ_243143,RMVar_hsa_circ_243145,RMVar_hsa_circ_243146,RMVar_hsa_circ_243144,RMVar_hsa_circ_243142,RMVar_hsa_circ_243140 94866 RMVar_ID_94866 Human_SNP_ID_306485936 m1A Human chr6 + 170400105 170400105 170400105 GAACTATGTCATAAGCCTTAGGAGTGAGTGAGAAAGGTAGAACTATGTCATAACCCTTAGGAGTG GAACTATGTCATAAGCCTTAGGAGTGAGTGAGGAAGGTAGAACTATGTCATAACCCTTAGGAGTG A G FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:170400085..170400169 26863410 MeRIP-seq:(Medium) rs1287975274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13315,Human_RBP_ID_1111235,Human_RBP_ID_5152268,Human_RBP_ID_5242751,Human_RBP_ID_5400073,Human_RBP_ID_5478639,Human_RBP_ID_15744867,Human_RBP_ID_21948483,Human_RBP_ID_23259203,Human_RBP_ID_24149646,Human_RBP_ID_24386960 RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_91561,RMVar_hsa_circ_243154,RMVar_hsa_circ_332497,RMVar_hsa_circ_45303,RMVar_hsa_circ_243156 94867 RMVar_ID_94867 Human_SNP_ID_306523099 m1A Human chr6 + 170535302 170535302 170535302 CTATGCAGATCCGGAGTGCGTCCCCAGTGTACACATCTCTCTCAGCCGCAGAAATGAAGACATCT CTATGCAGATCCGGAGTGCGTCCCCAGTGTACTCATCTCTCTCAGCCGCAGAAATGAAGACATCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:170535251..170535366 26863196 MeRIP-seq:(Medium) rs767087766 Functional Loss SNV dbSNP153 33..33 33 - - - 94868 RMVar_ID_94868 Human_SNP_ID_306525765 m1A Human chr6 - 170546159 170546159 170546159 TTTACAGAACAGACAAAACAGTCATTGGATGCAGCGGTTTTCATGGAGACTGTCTTACGCTGACA TTTACAGAACAGACAAAACAGTCATTGGATGCGGCGGTTTTCATGGAGACTGTCTTACGCTGACA T C PSMB1 Ensembl:ENSG00000008018 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:170535165..170546165 32194978 MeRIP-seq:(Medium) rs1289256838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78811,Human_RBP_ID_657709,Human_RBP_ID_950335,Human_RBP_ID_1667633,Human_RBP_ID_2015103,Human_RBP_ID_8638431,Human_RBP_ID_9192134,Human_RBP_ID_9403065,Human_RBP_ID_15745705,Human_RBP_ID_17309331,Human_RBP_ID_17663863,Human_RBP_ID_18086065,Human_RBP_ID_18859314,Human_RBP_ID_22462350,Human_RBP_ID_24149767 Human_Splice_Rec_835714,Human_Splice_Rec_835715,Human_Splice_Rec_835722,Human_Splice_Rec_835723 RMVar_hsa_circ_109293,RMVar_hsa_circ_125903,RMVar_hsa_circ_243157,RMVar_hsa_circ_243158,RMVar_hsa_circ_243159,RMVar_hsa_circ_243166,RMVar_hsa_circ_243163,RMVar_hsa_circ_243165,RMVar_hsa_circ_92612,RMVar_hsa_circ_243164,RMVar_hsa_circ_243167,RMVar_hsa_circ_278468,RMVar_hsa_circ_358936,RMVar_hsa_circ_243168,RMVar_hsa_circ_243169,RMVar_hsa_circ_294725,RMVar_hsa_circ_368351,RMVar_hsa_circ_243170,RMVar_hsa_circ_243171,RMVar_hsa_circ_292714,RMVar_hsa_circ_243172 94869 RMVar_ID_94869 Human_SNP_ID_306527678 m1A Human chr6 + 170553239 170553239 170553239 GCCAGGAGCCGAATACATGGCTGTAGAGGACAACATCGCACGGCTGCGCCTGCGGATCCGACACT GCCAGGAGCCGAATACATGGCTGTAGAGGACACCATCGCACGGCTGCGCCTGCGGATCCGACACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:170553189..170553300 26863196 MeRIP-seq:(Medium) rs761244885 Functional Loss SNV dbSNP153 33..33 33 - - - 94870 RMVar_ID_94870 Human_SNP_ID_306529888 m1A Human chr6 + 170561924 170561910 170561925 GGAAGAGCAACAAAGGCAGCAGCAGCAACAACAACAGCAGCAGCAGCAGCAGCAGCAGCAACAGC GGAAGAGCAACAAAGGCAG_______________CAGCAGCAGCAGCAGCAGCAGCAGCAACAGC GCAGCAGCAACAACAA G TBP Ensembl:ENSG00000112592 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs755629023 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_27828192 RMVar_hsa_circ_19194,RMVar_hsa_circ_285689 94871 RMVar_ID_94871 Human_SNP_ID_306535674 m1A Human chr6 + 170583747 170583747 170583747 AATCGTTTTTCCTGGGTAGTTGATTCCTAAAAACTAAAAAAGAATACAGAGAAAAGTTTTATCTT AATCGTTTTTCCTGGGTAGTTGATTCCTAAAATCTAAAAAAGAATACAGAGAAAAGTTTTATCTT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:170583149..170584072 32194978 MeRIP-seq:(Medium) rs148653243 Functional Loss SNV dbSNP153 33..33 33 - - - 94872 RMVar_ID_94872 Human_SNP_ID_306535903 m1A Human chr6 + 170584350 170584350 170584350 CGGCTGCTCGCGGCAGCAGAAGAGGAAGATGCAGCGGTGGAAGGCGTCCGGGCGGCCAGGCAGCG CGGCTGCTCGCGGCAGCAGAAGAGGAAGATGCTGCGGTGGAAGGCGTCCGGGCGGCCAGGCAGCG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:170584221..170584443 32194978 MeRIP-seq:(Medium) rs751128316 Functional Loss SNV dbSNP153 33..33 33 - - - 94873 RMVar_ID_94873 Human_SNP_ID_306535905 m1A Human chr6 + 170584358 170584358 170584358 CGCGGCAGCAGAAGAGGAAGATGCAGCGGTGGAAGGCGTCCGGGCGGCCAGGCAGCGGCGCATAC CGCGGCAGCAGAAGAGGAAGATGCAGCGGTGGGAGGCGTCCGGGCGGCCAGGCAGCGGCGCATAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:170584289..170584376 26863196 MeRIP-seq:(Medium) rs1216934637 Functional Loss SNV dbSNP153 33..33 33 - - - 94874 RMVar_ID_94874 Human_SNP_ID_306535962 m1A Human chr6 - 170584474 170584448 170584475 CAGTTCCCCAGCAAGGTGGGCGGGCGGCCGGCATGGCTGGGCGCGGCCGGGCTGCCGGGGCCCCA CAGTTCCCCAGCAAGGTGGGCGGGCGGCCGG___________________________GGCCCCA CCCGGCAGCCCGGCCGCGCCCAGCCATG C PDCD2 Ensembl:ENSG00000071994 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:170584436..170584602 26863196 MeRIP-seq:(Medium) rs759988711 Functional Loss DEL dbSNP153 32..58 33 - - - Human_RBP_ID_840553,Human_RBP_ID_951177,Human_RBP_ID_4874091,Human_RBP_ID_5242641,Human_RBP_ID_5477647,Human_RBP_ID_9309898,Human_RBP_ID_9336404,Human_RBP_ID_17664242,Human_RBP_ID_18070097 Human_miRNA_ID_2577140 RMVar_hsa_circ_83712,RMVar_hsa_circ_243176,RMVar_hsa_circ_243179,RMVar_hsa_circ_111454 94875 RMVar_ID_94875 Human_SNP_ID_306535967 m1A Human chr6 + 170584454 170584454 170584454 ACAGCTCGCAGGCCAGGGCCTGGGGCCCCGGCAGCCCGGCCGCGCCCAGCCATGCCGGCCGCCCG ACAGCTCGCAGGCCAGGGCCTGGGGCCCCGGCGGCCCGGCCGCGCCCAGCCATGCCGGCCGCCCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:170584365..170584650 26863410 MeRIP-seq:(Medium) rs947729536 Functional Loss SNV dbSNP153 33..33 33 - - - 94876 RMVar_ID_94876 Human_SNP_ID_650233225 m1A Human chr18 - 62187627 62187627 62187627 CAGAGCCAGGATCTAGGCCACTTCCGGCGCCCAGCCGAAGTACTGCCCGCCGTTCCTCTGTTGCA CAGAGCCAGGATCTAGGCCACTTCCGGCGCCCCGCCGAAGTACTGCCCGCCGTTCCTCTGTTGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:62187582..62187688 26863196 MeRIP-seq:(Medium) rs758174003 Functional Loss SNV dbSNP153 33..33 33 - - - 94877 RMVar_ID_94877 Human_SNP_ID_650233241 m1A Human chr18 - 62187669 62187669 62187669 TGCTTCCTAAGGCCACGGGATCCTGTGGCGACAGCGAGCCCGCAGAGCCAGGATCTAGGCCACTT TGCTTCCTAAGGCCACGGGATCCTGTGGCGACGGCGAGCCCGCAGAGCCAGGATCTAGGCCACTT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:62187619..62187751 26863196 MeRIP-seq:(Medium) rs1292946832 Functional Loss SNV dbSNP153 33..33 33 - - - 94878 RMVar_ID_94878 Human_SNP_ID_650233242 m1A Human chr18 - 62187669 62187669 62187669 TGCTTCCTAAGGCCACGGGATCCTGTGGCGACAGCGAGCCCGCAGAGCCAGGATCTAGGCCACTT TGCTTCCTAAGGCCACGGGATCCTGTGGCGACCGCGAGCCCGCAGAGCCAGGATCTAGGCCACTT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:62187619..62187751 26863196 MeRIP-seq:(Medium) rs1292946832 Functional Loss SNV dbSNP153 33..33 33 - - - 94879 RMVar_ID_94879 Human_SNP_ID_650309444 m1A Human chr18 + 62522794 62522794 62522794 CGCACGCTCCTCACCGCTCCCGGGCTACCCTCACGCCGCCCCACGGCCCCAGCCCGCGTCCTCCT CGCACGCTCCTCACCGCTCCCGGGCTACCCTCTCGCCGCCCCACGGCCCCAGCCCGCGTCCTCCT A T NONHSAG024039.2 RNACentral:URS00009B50F2 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:62522657..62522813 26863196 MeRIP-seq:(Medium) rs1052244961 Functional Loss SNV dbSNP153 33..33 33 - - - 94880 RMVar_ID_94880 Human_SNP_ID_650309624 m1A Human chr18 + 62523123 62523123 62523123 GCTCAGCGCGGACGGCGGAGAGAGGGAGGCGGAAGGAGGACACCCTCGCTCGCTTGCTCCCACCC GCTCAGCGCGGACGGCGGAGAGAGGGAGGCGGCAGGAGGACACCCTCGCTCGCTTGCTCCCACCC A C ZCCHC2 Ensembl:ENSG00000141664 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:62523015..62523239 26863196 MeRIP-seq:(Medium) rs965395964 Functional Loss SNV dbSNP153 33..33 33 - - - 94881 RMVar_ID_94881 Human_SNP_ID_650309630 m1A Human chr18 + 62523132 62523132 62523132 GGACGGCGGAGAGAGGGAGGCGGAAGGAGGACACCCTCGCTCGCTTGCTCCCACCCGCACCCGGG GGACGGCGGAGAGAGGGAGGCGGAAGGAGGACTCCCTCGCTCGCTTGCTCCCACCCGCACCCGGG A T ZCCHC2 Ensembl:ENSG00000141664 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:62523083..62523243 26863196 MeRIP-seq:(Medium) rs1454281058 Functional Loss SNV dbSNP153 33..33 33 - - - 94882 RMVar_ID_94882 Human_SNP_ID_650310004 m1A Human chr18 + 62523708 62523708 62523708 CGGCGGGGGGCCCTCGGCGGCGCTGCGCGAGCAGGAGCGGGTATACGAGTGGTTCGGGCTGGTGC CGGCGGGGGGCCCTCGGCGGCGCTGCGCGAGCGGGAGCGGGTATACGAGTGGTTCGGGCTGGTGC A G ZCCHC2 Ensembl:ENSG00000141664 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:62523659..62523799 26863196 MeRIP-seq:(Medium) rs1555783802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22589693,Human_RBP_ID_22718029,Human_RBP_ID_26783256 94883 RMVar_ID_94883 Human_SNP_ID_650310200 m1A Human chr18 + 62524122 62524099 62524123 CGAGGACGGCGACGGCGAGCAGGACGCCGAGAAGGACGGCTCAGGCCCGGAAGGCGGCATTGTGG CGAGGACGGC________________________GACGGCTCAGGCCCGGAAGGCGGCATTGTGG CGACGGCGAGCAGGACGCCGAGAAG C ZCCHC2 Ensembl:ENSG00000141664 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:62524073..62524214 26863196 MeRIP-seq:(Medium) rs1320517945 Functional Loss DEL dbSNP153 11..34 33 - - - 94884 RMVar_ID_94884 Human_SNP_ID_650327364 m1A Human chr18 - 62587866 62587866 62587866 GCCACCCTCCGCCTGCCCCAAGTACAACGGGCAACTCCACCTTCACAGCTCCCATCTGCCTAGGC GCCACCCTCCGCCTGCCCCAAGTACAACGGGCGACTCCACCTTCACAGCTCCCATCTGCCTAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:62587821..62587913 26863196 MeRIP-seq:(Medium) rs923359526 Functional Loss SNV dbSNP153 33..33 33 - - - 94885 RMVar_ID_94885 Human_SNP_ID_650359115 m1A Human chr18 - 62715589 62715589 62715589 AGGCGGAGGTGGGAGACGGCGGCGGCGCGCGGAGAAGGGAGAAGCCAATGGCGTTGTGCGCGGCC AGGCGGAGGTGGGAGACGGCGGCGGCGCGCGGGGAAGGGAGAAGCCAATGGCGTTGTGCGCGGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:62715542..62715674 26863196 MeRIP-seq:(Medium) rs1031684749 Functional Loss SNV dbSNP153 33..33 33 - - - 94886 RMVar_ID_94886 Human_SNP_ID_650359130 m1A Human chr18 - 62715629 62715629 62715629 CCCCCAGCTCCGGAGGCAGCGGGCGGAGAGGGAGGCGATGAGGCGGAGGTGGGAGACGGCGGCGG CCCCCAGCTCCGGAGGCAGCGGGCGGAGAGGGGGGCGATGAGGCGGAGGTGGGAGACGGCGGCGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:62715549..62715704 26863196 MeRIP-seq:(Medium) rs1398833163 Functional Loss SNV dbSNP153 33..33 33 - - - 94887 RMVar_ID_94887 Human_SNP_ID_650364628 m1A Human chr18 + 62737193 62737193 62737193 CTGGGAAAGATTCTCTGAGAAAATGAGAGACTAGCATTGCATGAAAAGGGCATGCCAGGTACTGC CTGGGAAAGATTCTCTGAGAAAATGAGAGACTGGCATTGCATGAAAAGGGCATGCCAGGTACTGC A G PHLPP1 Ensembl:ENSG00000081913 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:62737177..62737367 26863196 MeRIP-seq:(Medium) rs1050856199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102066,RMVar_hsa_circ_190539 94888 RMVar_ID_94888 Human_SNP_ID_650399024 m1A Human chr18 - 62879892 62879892 62879892 AACATGAGTAGGAGTTCAATAGACAGAGGGGGACTGGAAGACAGACCATTTAAAAAGAATCGTAT AACATGAGTAGGAGTTCAATAGACAGAGGGGGGCTGGAAGACAGACCATTTAAAAAGAATCGTAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:62879764..62879978 26863196 MeRIP-seq:(Medium) rs955674025 Functional Loss SNV dbSNP153 33..33 33 - - - 94889 RMVar_ID_94889 Human_SNP_ID_650477223 m1A Human chr18 - 63198393 63198393 63198393 GTGTCTCTGTGTCTATGTGTGTCTGTGTGTCAATGGGTGTCTGTGTGTGTCTATGTCAGTGTGTG GTGTCTCTGTGTCTATGTGTGTCTGTGTGTCAGTGGGTGTCTGTGTGTGTCTATGTCAGTGTGTG T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:63198278..63198409 26863196 MeRIP-seq:(Medium) rs1388732848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23775881 94890 RMVar_ID_94890 Human_SNP_ID_650477424 m1A Human chr18 + 63198646 63198645 63198647 ACTGACACACAGACACAGAGACACACACACAGACATACACAGACACACACAGACACAAAGACACA ACTGACACACAGACACAGAGACACACACACAG__ATACACAGACACACACAGACACAAAGACACA GAC G HSALNG0122033 RNACentral:URS0000E98B7C lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:63198263..63199011 26863196 MeRIP-seq:(Medium) rs1457983601 Functional Loss DEL dbSNP153 33..34 33 - - - 94891 RMVar_ID_94891 Human_SNP_ID_650477426 m1A Human chr18 + 63198652 63198649 63198653 ACACAGACACAGAGACACACACACAGACATACACAGACACACACAGACACAAAGACACAACAGAC ACACAGACACAGAGACACACACACAGACAT____AGACACACACAGACACAAAGACACAACAGAC TACAC T HSALNG0122033 RNACentral:URS0000E98B7C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63198224..63199090 26863196 MeRIP-seq:(Medium) rs1313283120 Functional Loss DEL dbSNP153 31..34 33 - - - 94892 RMVar_ID_94892 Human_SNP_ID_650477690 m1A Human chr18 + 63198925 63198924 63198926 ACACACACACAGACATATACAGACACACACAGACACAGAGACACACACTGACACAGAGACACACA ACACACACACAGACATATACAGACACACACAG__ACAGAGACACACACTGACACAGAGACACACA GAC G HSALNG0122033 RNACentral:URS0000E98B7C lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr18:63198843..63199093;chr18:63198843..63198978 26863196 MeRIP-seq:(Medium) rs1568231618 Functional Loss DEL dbSNP153 33..34 33 - - - 94893 RMVar_ID_94893 Human_SNP_ID_650482654 m1A Human chr18 + 63218639 63218639 63218639 CACTCATCCCCCTCCACTCATCCCATCCACTCATCCCATCCTCCACTCATCCCCATCCTCCAGTC CACTCATCCCCCTCCACTCATCCCATCCACTCCTCCCATCCTCCACTCATCCCCATCCTCCAGTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:63218562..63218852 26863196 MeRIP-seq:(Medium) rs916115110 Functional Loss SNV dbSNP153 33..33 33 - - - 94894 RMVar_ID_94894 Human_SNP_ID_650482669 m1A Human chr18 + 63218678 63218659 63218679 CCTCCACTCATCCCCATCCTCCAGTCATCCCCATCCTCCACTCATCCCATTCTCCACTCATCCCC CCTCCACTCATCCC____________________CCTCCACTCATCCCATTCTCCACTCATCCCC CCATCCTCCAGTCATCCCCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:63218534..63218965;chr18:63218452..63219023;chr18:63218539..63218953 26863196 MeRIP-seq:(Medium) rs1258503773 Functional Loss DEL dbSNP153 15..34 33 - - - 94895 RMVar_ID_94895 Human_SNP_ID_650485258 m1A Human chr18 - 63229517 63229516 63229517 ATGTCATGAGAACTCACTATCACAAAGAAGACACCAAGGGGATAGTGCTAAACCATTCATGAGAA ATGTCATGAGAACTCACTATCACAAAGAAGAC_CCAAGGGGATAGTGCTAAACCATTCATGAGAA GT G BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63229514..63229659 26863196 MeRIP-seq:(Medium) rs1429706483 Functional Loss DEL dbSNP153 33..33 33 - - - 94896 RMVar_ID_94896 Human_SNP_ID_650496405 m1A Human chr18 + 63277024 63277024 63277024 TGGGTCTGGCCAGGGCTGCTTTCCTCCATCTCATTTCCCGCCACTTTCCCTCCCTCCCACTGCAA TGGGTCTGGCCAGGGCTGCTTTCCTCCATCTCGTTTCCCGCCACTTTCCCTCCCTCCCACTGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63277016..63277161 26863196 MeRIP-seq:(Medium) rs1383907610 Functional Loss SNV dbSNP153 33..33 33 - - - 94897 RMVar_ID_94897 Human_SNP_ID_650496417 m1A Human chr18 - 63277072 63277072 63277072 GAGGGTCCAGGACAAAGGCTGGGCATGCCAACAGGGGAGAAAGAGGTATTGCAGTGGGAGGGAGG GAGGGTCCAGGACAAAGGCTGGGCATGCCAACGGGGGAGAAAGAGGTATTGCAGTGGGAGGGAGG T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63277050..63277178 26863196 MeRIP-seq:(Medium) rs1449520031 Functional Loss SNV dbSNP153 33..33 33 - - - 94898 RMVar_ID_94898 Human_SNP_ID_650500817 m1A Human chr18 + 63295688 63295688 63295688 AAATGTCCTCAACAACTACACAGCTCTCACCCATATCCACCTCCTCTTCTTGATCAATTCTCTCT AAATGTCCTCAACAACTACACAGCTCTCACCCCTATCCACCTCCTCTTCTTGATCAATTCTCTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63295650..63295848 26863196 MeRIP-seq:(Medium) rs1168433775 Functional Loss SNV dbSNP153 33..33 33 - - - 94899 RMVar_ID_94899 Human_SNP_ID_650503965 m1A Human chr18 - 63309553 63309553 63309553 TGGAACAGAAAGGACAGGACAGATGTGGGCACACTGCACGTGTAGAATCAAAGGACTGACAGCAG TGGAACAGAAAGGACAGGACAGATGTGGGCACGCTGCACGTGTAGAATCAAAGGACTGACAGCAG T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:63309507..63309640 26863196 MeRIP-seq:(Medium) rs1001045146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1551349,Human_RBP_ID_13330246 94900 RMVar_ID_94900 Human_SNP_ID_650505808 m1A Human chr18 + 63318007 63318007 63318007 TCGCCGGCTCCACAGCCTCCCATTGCCCCAGGAGCCCACCCGCACTCCAACCCCCGCATCTCGGA TCGCCGGCTCCACAGCCTCCCATTGCCCCAGGTGCCCACCCGCACTCCAACCCCCGCATCTCGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63317961..63318183 26863196 MeRIP-seq:(Medium) rs557876106 Functional Loss SNV dbSNP153 33..33 33 - - - 94901 RMVar_ID_94901 Human_SNP_ID_650505833 m1A Human chr18 + 63318051 63318051 63318051 CTCCAACCCCCGCATCTCGGACCTGTGGCCTCAGCCCAGACTCACATCACCAAGTGCACCTACCC CTCCAACCCCCGCATCTCGGACCTGTGGCCTCGGCCCAGACTCACATCACCAAGTGCACCTACCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:63318001..63318112 26863196 MeRIP-seq:(Medium) rs748213542 Functional Loss SNV dbSNP153 33..33 33 - - - 94902 RMVar_ID_94902 Human_SNP_ID_650506367 m1A Human chr18 - 63319892 63319892 63319892 ACCAGGAGGAGGAGAAAGGGTGCGCAGCCCGGAGGCGGGGTGCGCCGGTGGGGTGCAGCGGAAGA ACCAGGAGGAGGAGAAAGGGTGCGCAGCCCGGGGGCGGGGTGCGCCGGTGGGGTGCAGCGGAAGA T C BCL2 Ensembl:ENSG00000171791 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:63319845..63320076;chr18:63319843..63320061 26863196 MeRIP-seq:(Medium) rs1328985209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17911835 94903 RMVar_ID_94903 Human_SNP_ID_650530642 m1A Human chr18 + 63418126 63418126 63418126 CCTCAGCAGAAAAATGTGTTGTCCTATCTCAGACTCACATCTGCAGAACACAAACTACACACCAT CCTCAGCAGAAAAATGTGTTGTCCTATCTCAGCCTCACATCTGCAGAACACAAACTACACACCAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63418124..63418325 26863196 MeRIP-seq:(Medium) rs1243569473 Functional Loss SNV dbSNP153 33..33 33 - - - 94904 RMVar_ID_94904 Human_SNP_ID_650530651 m1A Human chr18 - 63418173 63418173 63418173 GAGATGAGTGAGATGTAGGGAGAGGAGAACCGAGGAGCTGAGGAGTGATGGTGTGTAGTTTGTGT GAGATGAGTGAGATGTAGGGAGAGGAGAACCGGGGAGCTGAGGAGTGATGGTGTGTAGTTTGTGT T C VPS4B Ensembl:ENSG00000119541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63418171..63418284 26863196 MeRIP-seq:(Medium) rs1411343575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23776093 94905 RMVar_ID_94905 Human_SNP_ID_650675136 m1A Human chr18 + 63970130 63970130 63970130 AGCATCTACAAAGGAGGAATAGTCAAAGCAGCAGCGGCGGCGGCGGCGGCGGCAGCAGCAGCAGC AGCATCTACAAAGGAGGAATAGTCAAAGCAGCGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCAGC A G SERPINB8,HMSD Ensembl:ENSG00000166401,Ensembl:ENSG00000221887 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:63970093..63970440;chr18:63970099..63970342 26863196 MeRIP-seq:(Medium) rs796245876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1923203,Human_Splice_Rec_1923215,Human_Splice_Rec_1923225,Human_Splice_Rec_1923237,Human_Splice_Rec_1923251 94906 RMVar_ID_94906 Human_SNP_ID_650677276 m1A Human chr18 - 63978265 63978265 63978265 TGCATCAAAGGCACAGCAGGGAAAAGCACATAAGCCAATGACTCCGGTAGCCACGCAGTCATTCA TGCATCAAAGGCACAGCAGGGAAAAGCACATATGCCAATGACTCCGGTAGCCACGCAGTCATTCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63978261..63978423 26863196 MeRIP-seq:(Medium) rs1026173076 Functional Loss SNV dbSNP153 33..33 33 - - - 94907 RMVar_ID_94907 Human_SNP_ID_650677277 m1A Human chr18 - 63978265 63978265 63978265 TGCATCAAAGGCACAGCAGGGAAAAGCACATAAGCCAATGACTCCGGTAGCCACGCAGTCATTCA TGCATCAAAGGCACAGCAGGGAAAAGCACATAGGCCAATGACTCCGGTAGCCACGCAGTCATTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:63978261..63978423 26863196 MeRIP-seq:(Medium) rs1026173076 Functional Loss SNV dbSNP153 33..33 33 - - - 94908 RMVar_ID_94908 Human_SNP_ID_651884080 m1A Human chr18 + 68676083 68676083 68676083 AAAAATATGATACATACCACTTTTCAAAAAGCAGAAGATTTTTATCAAAGGAAATGTTAGAAGAA AAAAATATGATACATACCACTTTTCAAAAAGCGGAAGATTTTTATCAAAGGAAATGTTAGAAGAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:68676033..68676134 32194978 MeRIP-seq:(Medium) rs1174387693 Functional Loss SNV dbSNP153 33..33 33 - - - 94909 RMVar_ID_94909 Human_SNP_ID_651884252 m1A Human chr18 - 68676824 68676824 68676824 ATGATCTTTACAGAAAAGAACATGTTATTCGTATTTTGCTAATATCAACTGCATGGATTAAAGTA ATGATCTTTACAGAAAAGAACATGTTATTCGTGTTTTGCTAATATCAACTGCATGGATTAAAGTA T C TMX3 Ensembl:ENSG00000166479 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:68676781..68677032 32194978 MeRIP-seq:(Medium) rs1216211694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9082666,Human_RBP_ID_22390800,Human_RBP_ID_24483074 RMVar_hsa_circ_190592,RMVar_hsa_circ_118208 94910 RMVar_ID_94910 Human_SNP_ID_651894600 m1A Human chr18 - 68714998 68714998 68714998 CTTTATCCCTCTTTTGCACAGTCAGCTTCTGCAGCTCTCCCGGGCTAGCATGGCAGCGTGGAAGA CTTTATCCCTCTTTTGCACAGTCAGCTTCTGCGGCTCTCCCGGGCTAGCATGGCAGCGTGGAAGA T C TMX3 Ensembl:ENSG00000166479 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:68714948..68715048 32194978 MeRIP-seq:(Medium) rs769459920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_510627,Human_RBP_ID_906015,Human_RBP_ID_4494043,Human_RBP_ID_18420680 Human_Splice_Rec_1923683,Human_Splice_Rec_1923715,Human_Splice_Rec_1923757,Human_Splice_Rec_1923773,Human_Splice_Rec_1923787,Human_Splice_Rec_1923801,Human_Splice_Rec_1923813,Human_Splice_Rec_1923841 94911 RMVar_ID_94911 Human_SNP_ID_652062838 m1A Human chr18 - 69400845 69400845 69400845 AGCGCACCACCGCGGCTCCCCGGCGCGGGGGGAGGGGGCGGGCCGGGGGGGGCGGGCTGATGCGC AGCGCACCACCGCGGCTCCCCGGCGCGGGGGGGGGGGGCGGGCCGGGGGGGGCGGGCTGATGCGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:69400751..69400864 26863196 MeRIP-seq:(Medium) rs905086049 Functional Loss SNV dbSNP153 33..33 33 - - - 94912 RMVar_ID_94912 Human_SNP_ID_652278167 m1A Human chr18 - 70289086 70289086 70289086 CTCCCGCCCGAGCTCCCCGGACGCTTACCCGGAGGCGGCCCGGCTCCGCTTCCTCGCCCAGCGCC CTCCCGCCCGAGCTCCCCGGACGCTTACCCGGGGGCGGCCCGGCTCCGCTTCCTCGCCCAGCGCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:70288921..70289352 26863196 MeRIP-seq:(Medium) rs1219685843 Functional Loss SNV dbSNP153 33..33 33 - - - 94913 RMVar_ID_94913 Human_SNP_ID_652281407 m1A Human chr18 + 70301303 70301303 70301303 ACTTATTAGGAGGTATTGCCATAATGCAGGAGAAAGAGGATGGTAGCTTGGACTAGTATAGTGGC ACTTATTAGGAGGTATTGCCATAATGCAGGAGTAAGAGGATGGTAGCTTGGACTAGTATAGTGGC A T SOCS6 Ensembl:ENSG00000170677 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:70301301..70301485 26863196 MeRIP-seq:(Medium) rs1161960644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13333384 94914 RMVar_ID_94914 Human_SNP_ID_652281469 m1A Human chr18 + 70301594 70301594 70301594 TGAACTTGTGAAGTTTCAGATATCTGCAAGACATCAAAGTGGCAGTGTCCTGAAGGGAGCTGAAT TGAACTTGTGAAGTTTCAGATATCTGCAAGACGTCAAAGTGGCAGTGTCCTGAAGGGAGCTGAAT A G SOCS6 Ensembl:ENSG00000170677 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:70301592..70302019 26863196 MeRIP-seq:(Medium) rs1032860316 Functional Loss SNV dbSNP153 33..33 33 - - - 94915 RMVar_ID_94915 Human_SNP_ID_652281534 m1A Human chr18 - 70301862 70301862 70301862 CCTAATCTTAGAGGCACTGTGTGTGACCACTGACCACTCCTTTTCCTTTCATATCATTTTACCTC CCTAATCTTAGAGGCACTGTGTGTGACCACTGGCCACTCCTTTTCCTTTCATATCATTTTACCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:70301859..70301981 26863196 MeRIP-seq:(Medium) rs1182619340 Functional Loss SNV dbSNP153 33..33 33 - - - 94916 RMVar_ID_94916 Human_SNP_ID_652287256 m1A Human chr18 + 70324544 70324542 70324544 ATATGACTCTTTTTATATTTTTATTTTTTAGAAAATGGCTCCAAAGGTTAAATGAAGCAGGAAAA ATATGACTCTTTTTATATTTTTATTTTTTAG__AATGGCTCCAAAGGTTAAATGAAGCAGGAAAA GAA G SOCS6 Ensembl:ENSG00000170677 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:70324531..70324605 26863196 MeRIP-seq:(Medium) rs1181097671 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1924826,Human_Splice_Rec_1924828,Human_Splice_Rec_1924830 RMVar_hsa_circ_190668 94917 RMVar_ID_94917 Human_SNP_ID_652287431 m1A Human chr18 - 70325015 70325015 70325015 GCGACGTGGACCTTATCGGCCTCTGAGCTCTCACGTCTTTAAAGACTATGGGTGCTGAGGAGGAG GCGACGTGGACCTTATCGGCCTCTGAGCTCTCCCGTCTTTAAAGACTATGGGTGCTGAGGAGGAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:70324964..70325164 32194978 MeRIP-seq:(Medium) rs750564600 Functional Loss SNV dbSNP153 33..33 33 - - - 94918 RMVar_ID_94918 Human_SNP_ID_652287675 m1A Human chr18 + 70325662 70325662 70325662 AAATCCAAAGGAACTTCAGTGGACTCACTGGCACAGAAGCCCACGTGGCTGAAAGTATGCGCTGT AAATCCAAAGGAACTTCAGTGGACTCACTGGCGCAGAAGCCCACGTGGCTGAAAGTATGCGCTGT A G SOCS6 Ensembl:ENSG00000170677 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:70325612..70325862 32194978 MeRIP-seq:(Medium) rs932798136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4491549 RMVar_hsa_circ_190668 94919 RMVar_ID_94919 Human_SNP_ID_653269182 m1A Human chr18 + 74148612 74148612 74148612 AGAGCCTGTTAATTAAAATGGAAAGAAGACAGAAGGGAAGGTAGACATCAGGTTCTCCCTGGAGA AGAGCCTGTTAATTAAAATGGAAAGAAGACAGGAGGGAAGGTAGACATCAGGTTCTCCCTGGAGA A G TIMM21 Ensembl:ENSG00000075336 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:74148563..74148656 26863196 MeRIP-seq:(Medium) rs545082000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3559371,Human_RBP_ID_6703742,Human_RBP_ID_13335583 94920 RMVar_ID_94920 Human_SNP_ID_653271007 m1A Human chr18 + 74155389 74155389 74155389 GCAAGATATATGGGAGAGCCTTAGAAAAATGCAGATCACATCCTGAGGTTAGTTCTCAAGATTGA GCAAGATATATGGGAGAGCCTTAGAAAAATGCTGATCACATCCTGAGGTTAGTTCTCAAGATTGA A T TIMM21 Ensembl:ENSG00000075336 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:74155338..74155438 32194978 MeRIP-seq:(Medium) rs747347327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_510740,Human_RBP_ID_1551735,Human_RBP_ID_2547965,Human_RBP_ID_17912257 Human_Splice_Rec_1925264,Human_Splice_Rec_1925265,Human_Splice_Rec_1925270,Human_Splice_Rec_1925271,Human_Splice_Rec_1925279,Human_Splice_Rec_1925284,Human_Splice_Rec_1925285,Human_Splice_Rec_1925292,Human_Splice_Rec_1925293 RMVar_hsa_circ_43174 94921 RMVar_ID_94921 Human_SNP_ID_653299279 m1A Human chr18 - 74263422 74263414 74263423 AAGGGAACAAGCTGGAGGTGACGCTACTGAGAACTTTGAGGATGTCGGGCACTCTACAGATGCCA AAGGGAACAAGCTGGAGGTGACGCTACTGAG_________GATGTCGGGCACTCTACAGATGCCA CCTCAAAGTT C CYB5A Ensembl:ENSG00000166347 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74263387..74263547 26863196 MeRIP-seq:(Medium) rs1341210125 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_769144,Human_RBP_ID_1551756,Human_RBP_ID_1878075,Human_RBP_ID_4491744,Human_RBP_ID_8474160,Human_RBP_ID_13335854,Human_RBP_ID_17655270,Human_RBP_ID_18719698,Human_RBP_ID_22064558,Human_RBP_ID_26814701,Human_RBP_ID_27814632 Human_Splice_Rec_1925300,Human_Splice_Rec_1925301,Human_Splice_Rec_1925312,Human_Splice_Rec_1925313,Human_Splice_Rec_1925320,Human_Splice_Rec_1925321,Human_Splice_Rec_1925330,Human_Splice_Rec_1925331,Human_Splice_Rec_1925336,Human_Splice_Rec_1925337 RMVar_hsa_circ_88202,RMVar_hsa_circ_190680 94922 RMVar_ID_94922 Human_SNP_ID_653299283 m1A Human chr18 - 74263422 74263422 74263422 AAGGGAACAAGCTGGAGGTGACGCTACTGAGAACTTTGAGGATGTCGGGCACTCTACAGATGCCA AAGGGAACAAGCTGGAGGTGACGCTACTGAGAGCTTTGAGGATGTCGGGCACTCTACAGATGCCA T C CYB5A Ensembl:ENSG00000166347 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74263387..74263547 26863196 MeRIP-seq:(Medium) rs1398570012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769144,Human_RBP_ID_1551756,Human_RBP_ID_1878075,Human_RBP_ID_4491744,Human_RBP_ID_8474160,Human_RBP_ID_13335854,Human_RBP_ID_17655270,Human_RBP_ID_18719698,Human_RBP_ID_22064558,Human_RBP_ID_26814701,Human_RBP_ID_27814632 Human_Splice_Rec_1925300,Human_Splice_Rec_1925301,Human_Splice_Rec_1925312,Human_Splice_Rec_1925313,Human_Splice_Rec_1925320,Human_Splice_Rec_1925321,Human_Splice_Rec_1925330,Human_Splice_Rec_1925331,Human_Splice_Rec_1925336,Human_Splice_Rec_1925337 RMVar_hsa_circ_88202,RMVar_hsa_circ_190680 94923 RMVar_ID_94923 Human_SNP_ID_653299304 m1A Human chr18 - 74263479 74263479 74263479 AAAAAAATTTTTATTCTACCTCTCCTTTGAACAGCATCCTGGTGGGGAAGAAGTTTTAAGGGAAC AAAAAAATTTTTATTCTACCTCTCCTTTGAACGGCATCCTGGTGGGGAAGAAGTTTTAAGGGAAC T C CYB5A Ensembl:ENSG00000166347 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:74263451..74263500 32194978 MeRIP-seq:(Medium) rs794728010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_906020 Clinvar_Rec_542 RMVar_hsa_circ_88202,RMVar_hsa_circ_190680 94924 RMVar_ID_94924 Human_SNP_ID_653311653 m1A Human chr18 - 74315070 74315070 74315070 GCCTCGTGGAGAACGGGACGTTTGAGAAAGACATGAAGGCGGTGAGAGTGGGCAGCCTCGTGCAT GCCTCGTGGAGAACGGGACGTTTGAGAAAGACGTGAAGGCGGTGAGAGTGGGCAGCCTCGTGCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74315021..74315145 26863196 MeRIP-seq:(Medium) rs1262425944 Functional Loss SNV dbSNP153 33..33 33 - - - 94925 RMVar_ID_94925 Human_SNP_ID_653357277 m1A Human chr18 + 74496401 74496401 74496401 ACGGAACCGGCGCCGCGCTTGCTGCTGGTAACAGGGCCTTGCCTAGTGGGCCTTCCTTCCCAGGT ACGGAACCGGCGCCGCGCTTGCTGCTGGTAACGGGGCCTTGCCTAGTGGGCCTTCCTTCCCAGGT A G CNDP2 Ensembl:ENSG00000133313 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:74496355..74496480 26863196 MeRIP-seq:(Medium) rs1373057868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4494261,Human_RBP_ID_19087311 Human_Splice_Rec_1925393,Human_Splice_Rec_1925401,Human_Splice_Rec_1925407,Human_Splice_Rec_1925427,Human_Splice_Rec_1925433,Human_Splice_Rec_1925443,Human_Splice_Rec_1925453,Human_Splice_Rec_1925455,Human_Splice_Rec_1925475,Human_Splice_Rec_1925483,Human_Splice_Rec_1925491 94926 RMVar_ID_94926 Human_SNP_ID_653384345 m1A Human chr18 - 74598371 74598371 74598371 CGGTGCAGGGGTGCGTCCCGAAGGAACGGGGGACTGTTTCTGCGCGGACAGGCGAACCCGGCAGG CGGTGCAGGGGTGCGTCCCGAAGGAACGGGGGGCTGTTTCTGCGCGGACAGGCGAACCCGGCAGG T C LINC00909 Ensembl:ENSG00000264247 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr18:74598251..74598377;chr18:74598327..74598458 26863196 MeRIP-seq:(Medium) rs1482758132 Functional Loss SNV dbSNP153 33..33 33 - - - 94927 RMVar_ID_94927 Human_SNP_ID_653390528 m1A Human chr18 - 74623299 74623288 74623300 TTTCACACATGCACTTACCCTCACGCACTCACACTTGCACTCAAACACGCAGTCTCACACTCATG TTTCACACATGCACTTACCCTCACGCACTCA____________AACACGCAGTCTCACACTCATG TTGAGTGCAAGTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74623294..74623377 26863196 MeRIP-seq:(Medium) rs1432713550 Functional Loss DEL dbSNP153 32..43 33 - - - 94928 RMVar_ID_94928 Human_SNP_ID_653390531 m1A Human chr18 - 74623299 74623297 74623299 TTTCACACATGCACTTACCCTCACGCACTCACACTTGCACTCAAACACGCAGTCTCACACTCATG TTTCACACATGCACTTACCCTCACGCACTCAC__TTGCACTCAAACACGCAGTCTCACACTCATG AGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74623294..74623377 26863196 MeRIP-seq:(Medium) rs890740311 Functional Loss DEL dbSNP153 33..34 33 - - - 94929 RMVar_ID_94929 Human_SNP_ID_653392563 m1A Human chr18 - 74631037 74631037 74631037 TTTATCTTTTCATCCTCATCATTTTCGGGTTTATTCTCACTATCCATCATTAATAAAGTGCTGAC TTTATCTTTTCATCCTCATCATTTTCGGGTTTTTTCTCACTATCCATCATTAATAAAGTGCTGAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74630966..74631077 26863196 MeRIP-seq:(Medium) rs748906984 Functional Loss SNV dbSNP153 33..33 33 - - - 94930 RMVar_ID_94930 Human_SNP_ID_653392564 m1A Human chr18 - 74631037 74631037 74631037 TTTATCTTTTCATCCTCATCATTTTCGGGTTTATTCTCACTATCCATCATTAATAAAGTGCTGAC TTTATCTTTTCATCCTCATCATTTTCGGGTTTCTTCTCACTATCCATCATTAATAAAGTGCTGAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:74630966..74631077 26863196 MeRIP-seq:(Medium) rs748906984 Functional Loss SNV dbSNP153 33..33 33 - - - 94931 RMVar_ID_94931 Human_SNP_ID_653412357 m1A Human chr18 + 74712898 74712898 74712898 GGGAGAGTGCTGGAGCATACAGAAGGAAGAAGACAGGAAGTCAGGGTTTGGTGGGAGAAAAATAG GGGAGAGTGCTGGAGCATACAGAAGGAAGAAGGCAGGAAGTCAGGGTTTGGTGGGAGAAAAATAG A G ZNF407 Ensembl:ENSG00000215421 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:74712788..74712936 26863196 MeRIP-seq:(Medium) rs943832749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6704351 RMVar_hsa_circ_267682,RMVar_hsa_circ_269158,RMVar_hsa_circ_296893,RMVar_hsa_circ_190685,RMVar_hsa_circ_56612,RMVar_hsa_circ_363240,RMVar_hsa_circ_63368 94932 RMVar_ID_94932 Human_SNP_ID_653472857 m1A Human chr18 - 74961077 74961077 74961077 TCTCCTATCCCTCCACCCAGTCCTCGCTCAGGACCTTCTCCTATCCCTCCACCCAGTCCTCACTC TCTCCTATCCCTCCACCCAGTCCTCGCTCAGGGCCTTCTCCTATCCCTCCACCCAGTCCTCACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:74961073..74961151 26863196 MeRIP-seq:(Medium) rs1169989463 Functional Loss SNV dbSNP153 33..33 33 - - - 94933 RMVar_ID_94933 Human_SNP_ID_587181354 m1A Human chr15 + 90001482 90001482 90001482 AAGAGAGGAGCCGGAGGGAGGGCGGCAGGAGCAGGCGGCGGGCGCGCGTGGAGGCGGGCGGCGGG AAGAGAGGAGCCGGAGGGAGGGCGGCAGGAGCGGGCGGCGGGCGCGCGTGGAGGCGGGCGGCGGG A G ZNF710 Ensembl:ENSG00000140548 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:90001409..90001561;chr15:90001438..90067677 26863196 MeRIP-seq:(Medium) rs547911226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355327,Human_RBP_ID_18418532,Human_RBP_ID_18458252 94934 RMVar_ID_94934 Human_SNP_ID_587181365 m1A Human chr15 - 90001498 90001498 90001498 GGGCTGCTGCTGTGCGCCCGCCGCCCGCCTCCACGCGCGCCCGCCGCCTGCTCCTGCCGCCCTCC GGGCTGCTGCTGTGCGCCCGCCGCCCGCCTCCGCGCGCGCCCGCCGCCTGCTCCTGCCGCCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90001404..90067658 26863196 MeRIP-seq:(Medium) rs1168112981 Functional Loss SNV dbSNP153 33..33 33 - - - 94935 RMVar_ID_94935 Human_SNP_ID_587198679 m1A Human chr15 + 90067518 90067518 90067518 GAGGAACAGGAGGTCTATGAGGTTTCTGTGCCAGGTGACGACAAGGACGCAGGGCCAGCAGAAGC GAGGAACAGGAGGTCTATGAGGTTTCTGTGCCGGGTGACGACAAGGACGCAGGGCCAGCAGAAGC A G ZNF710 Ensembl:ENSG00000140548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90067090..90067598 26863196 MeRIP-seq:(Medium) rs1312110780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6478943 RMVar_hsa_circ_111859,RMVar_hsa_circ_290626,RMVar_hsa_circ_174715,RMVar_hsa_circ_95129,RMVar_hsa_circ_375823,RMVar_hsa_circ_174714,RMVar_hsa_circ_370951,RMVar_hsa_circ_174717,RMVar_hsa_circ_174718,RMVar_hsa_circ_174716 94936 RMVar_ID_94936 Human_SNP_ID_587203538 m1A Human chr15 + 90084805 90084805 90084805 CCCACATGGCCCCAGGGTCTGCCTACCACCCCAGGCCACGCACTTGCTGAGGCCGTGAATGCAGC CCCACATGGCCCCAGGGTCTGCCTACCACCCCGGGCCACGCACTTGCTGAGGCCGTGAATGCAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90084801..90084875 32194978 MeRIP-seq:(Medium) rs200898927 Functional Loss SNV dbSNP153 33..33 33 - - - 94937 RMVar_ID_94937 Human_SNP_ID_587208642 m1A Human chr15 + 90102314 90102314 90102314 GCCGCGGCTGCTCTTGCGAGGTGGGGGCTGTCAGGGCCGCCGGCGCCCAGGCCGGCCGCGAGCCT GCCGCGGCTGCTCTTGCGAGGTGGGGGCTGTCGGGGCCGCCGGCGCCCAGGCCGGCCGCGAGCCT A G IDH2-DT RNACentral:URS0000BC45DA lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:90102285..90102451 26863196 MeRIP-seq:(Medium) rs1212451541 Functional Loss SNV dbSNP153 33..33 33 - - - 94938 RMVar_ID_94938 Human_SNP_ID_587208669 m1A Human chr15 + 90102359 90102359 90102359 CCCAGGCCGGCCGCGAGCCTGAGGCTCTGCAGAGCGAGCGCACGACCCGCAGGTAGCCGGCCATC CCCAGGCCGGCCGCGAGCCTGAGGCTCTGCAGCGCGAGCGCACGACCCGCAGGTAGCCGGCCATC A C IDH2-DT RNACentral:URS0000BC45DA lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90102309..90102456 26863196 MeRIP-seq:(Medium) rs1258065873 Functional Loss SNV dbSNP153 33..33 33 - - - 94939 RMVar_ID_94939 Human_SNP_ID_587208678 m1A Human chr15 + 90102377 90102377 90102377 CTGAGGCTCTGCAGAGCGAGCGCACGACCCGCAGGTAGCCGGCCATCCCAAGCTGGAGAGCGAAC CTGAGGCTCTGCAGAGCGAGCGCACGACCCGCGGGTAGCCGGCCATCCCAAGCTGGAGAGCGAAC A G IDH2-DT RNACentral:URS0000BC45DA lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr15:90102276..90102475;chr15:90102326..90102400 26863410,32194978 MeRIP-seq:(Medium) rs766605461 Functional Loss SNV dbSNP153 33..33 33 - - - 94940 RMVar_ID_94940 Human_SNP_ID_587208679 m1A Human chr15 + 90102377 90102377 90102377 CTGAGGCTCTGCAGAGCGAGCGCACGACCCGCAGGTAGCCGGCCATCCCAAGCTGGAGAGCGAAC CTGAGGCTCTGCAGAGCGAGCGCACGACCCGCTGGTAGCCGGCCATCCCAAGCTGGAGAGCGAAC A T IDH2-DT RNACentral:URS0000BC45DA lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr15:90102276..90102475;chr15:90102326..90102400 26863410,32194978 MeRIP-seq:(Medium) rs766605461 Functional Loss SNV dbSNP153 33..33 33 - - - 94941 RMVar_ID_94941 Human_SNP_ID_587208702 m1A Human chr15 + 90102424 90102424 90102424 CCAAGCTGGAGAGCGAACGAGCAGGGCGGGAGAGGTCCGAGCGCGCGCCGCTCCTCCCGGCTGCC CCAAGCTGGAGAGCGAACGAGCAGGGCGGGAGCGGTCCGAGCGCGCGCCGCTCCTCCCGGCTGCC A C IDH2-DT RNACentral:URS0000BC45DA lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90102339..90102430 26863196 MeRIP-seq:(Medium) rs1460014634 Functional Loss SNV dbSNP153 33..33 33 - - - 94942 RMVar_ID_94942 Human_SNP_ID_587208715 m1A Human chr15 - 90102446 90102446 90102446 GCCCAGCGTTAGCCCGCGGCCAGGCAGCCGGGAGGAGCGGCGCGCGCTCGGACCTCTCCCGCCCT GCCCAGCGTTAGCCCGCGGCCAGGCAGCCGGGGGGAGCGGCGCGCGCTCGGACCTCTCCCGCCCT T C IDH2 Ensembl:ENSG00000182054 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:90102355..90102455 26863410 MeRIP-seq:(Medium) rs1330114413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759747,Human_RBP_ID_4342925,Human_RBP_ID_9324407 94943 RMVar_ID_94943 Human_SNP_ID_587231962 m1A Human chr15 - 90185023 90185023 90185023 GTCATCGCCCCCCGCGGGGCCGCTCTTCCTGGAGTGTCCACTGACTCGTCCCCCTTGCCAGGCCG GTCATCGCCCCCCGCGGGGCCGCTCTTCCTGGCGTGTCCACTGACTCGTCCCCCTTGCCAGGCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90184972..90185142 26863196 MeRIP-seq:(Medium) rs1356602123 Functional Loss SNV dbSNP153 33..33 33 - - - 94944 RMVar_ID_94944 Human_SNP_ID_587235968 m1A Human chr15 - 90199221 90199221 90199221 GTTCTCCCCGTTTCCTCCTTGGTTCCCCTACAATCTATTCTCAACACAGCAGCTGGAGTGAGTCT GTTCTCCCCGTTTCCTCCTTGGTTCCCCTACAGTCTATTCTCAACACAGCAGCTGGAGTGAGTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90199218..90199349 26863196 MeRIP-seq:(Medium) rs1441841456 Functional Loss SNV dbSNP153 33..33 33 - - - 94945 RMVar_ID_94945 Human_SNP_ID_587236579 m1A Human chr15 + 90201508 90201485 90201508 CCGGGGCGACTCGGGGGCGGACCGCGGGGCGGAGCTGCCGCCCGTGAGTCCGGCCGAGCCACCTG CCGGGGCGAC_______________________GCTGCCGCCCGTGAGTCCGGCCGAGCCACCTG CTCGGGGGCGGACCGCGGGGCGGA C SEMA4B Ensembl:ENSG00000185033 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:90201374..90201720;chr15:90201385..90201677 26863196 MeRIP-seq:(Medium) rs1199332907 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_815490,Human_RBP_ID_4342469 Human_Splice_Rec_1643622,Human_Splice_Rec_1643642,Human_Splice_Rec_1643670,Human_Splice_Rec_1643676 RMVar_hsa_circ_127929,RMVar_hsa_circ_90524,RMVar_hsa_circ_174728,RMVar_hsa_circ_174729 94946 RMVar_ID_94946 Human_SNP_ID_587238907 m1A Human chr15 - 90210072 90210072 90210072 TTCCCCTCACCATCCCCACTACCGCAGTCCTGAGCCTGGCACCATCCTCTCTCACCTAGGCCACC TTCCCCTCACCATCCCCACTACCGCAGTCCTGGGCCTGGCACCATCCTCTCTCACCTAGGCCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90210066..90210163 26863196 MeRIP-seq:(Medium) rs1346321070 Functional Loss SNV dbSNP153 33..33 33 - - - 94947 RMVar_ID_94947 Human_SNP_ID_587243755 m1A Human chr15 - 90225771 90225771 90225771 AGGCTGACGTGCTTGCAGCTGGAGCCGCTCCAAGCACAGTAGGGGTCCCGGGCGAGGAGGCAGTC AGGCTGACGTGCTTGCAGCTGGAGCCGCTCCACGCACAGTAGGGGTCCCGGGCGAGGAGGCAGTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90225721..90227282 32194978 MeRIP-seq:(Medium) rs1359060676 Functional Loss SNV dbSNP153 33..33 33 - - - 94948 RMVar_ID_94948 Human_SNP_ID_587244981 m1A Human chr15 + 90229478 90229478 90229478 CCTCGCTCCATCTTTGAACTCAAACACGAGGAACTAACTGCACCCTGGTCCTCTCCCCAGTCCCC CCTCGCTCCATCTTTGAACTCAAACACGAGGAGCTAACTGCACCCTGGTCCTCTCCCCAGTCCCC A G SEMA4B Ensembl:ENSG00000185033 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90229428..90229493 26863196 MeRIP-seq:(Medium) rs1302549880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18938039,Human_RBP_ID_26438388 RMVar_hsa_circ_107082,RMVar_hsa_circ_174742 94949 RMVar_ID_94949 Human_SNP_ID_587245446 m1A Human chr15 + 90231018 90231018 90231018 TGGTTCCATCCCTGTCAATGTCAGACTCCTCCAGGATCTGGGAAAGGGAGAGTTTCAGGCCAGAG TGGTTCCATCCCTGTCAATGTCAGACTCCTCCTGGATCTGGGAAAGGGAGAGTTTCAGGCCAGAG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90230315..90231025 32194978 MeRIP-seq:(Medium) rs1018739778 Functional Loss SNV dbSNP153 33..33 33 - - - 94950 RMVar_ID_94950 Human_SNP_ID_587245545 m1A Human chr15 - 90231196 90231196 90231196 GTGTCTGCTCTCTAGACTTTGATGATGACGGAACCTTGAACAGAGAAGACCTGAGCCGGCTGGTG GTGTCTGCTCTCTAGACTTTGATGATGACGGAGCCTTGAACAGAGAAGACCTGAGCCGGCTGGTG T C CIB1 Ensembl:ENSG00000185043 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90231076..90231500 32194978 MeRIP-seq:(Medium) rs773449398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466825,Human_RBP_ID_5113225,Human_RBP_ID_12634592,Human_RBP_ID_18982651,Human_RBP_ID_22497025,Human_RBP_ID_25178160 Human_Splice_Rec_1643814,Human_Splice_Rec_1643826,Human_Splice_Rec_1643838 Human_miRNA_ID_3118417 RMVar_hsa_circ_83623,RMVar_hsa_circ_102799,RMVar_hsa_circ_118811,RMVar_hsa_circ_85101,RMVar_hsa_circ_174746,RMVar_hsa_circ_174747,RMVar_hsa_circ_174748,RMVar_hsa_circ_174745,RMVar_hsa_circ_174750,RMVar_hsa_circ_92564,RMVar_hsa_circ_372832,RMVar_hsa_circ_174749 94951 RMVar_ID_94951 Human_SNP_ID_587246352 m1A Human chr15 - 90233836 90233836 90233836 TCGCCTGTCCAAGGAGCTGCTGGCCGAGTACCAGGTGCGCGGGACGCCTGGCCCTGGGGAGCTCG TCGCCTGTCCAAGGAGCTGCTGGCCGAGTACCGGGTGCGCGGGACGCCTGGCCCTGGGGAGCTCG T C CIB1 Ensembl:ENSG00000185043 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90233826..90233900 32194978 MeRIP-seq:(Medium) rs1208188220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342470,Human_RBP_ID_5316335,Human_RBP_ID_19068904 Human_Splice_Rec_1643807,Human_Splice_Rec_1643819 RMVar_hsa_circ_85101,RMVar_hsa_circ_174748 94952 RMVar_ID_94952 Human_SNP_ID_587246360 m1A Human chr15 + 90233851 90233851 90233851 CAGGCGTCCCGCGCACCTGGTACTCGGCCAGCAGCTCCTTGGACAGGCGACTGCCCGAGCCCCCC CAGGCGTCCCGCGCACCTGGTACTCGGCCAGCTGCTCCTTGGACAGGCGACTGCCCGAGCCCCCC A T GDPGP1 Ensembl:ENSG00000183208 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90232401..90233852 32194978 MeRIP-seq:(Medium) rs1402203366 Functional Loss SNV dbSNP153 33..33 33 - - - 94953 RMVar_ID_94953 Human_SNP_ID_587246370 m1A Human chr15 + 90233876 90233876 90233876 GGCCAGCAGCTCCTTGGACAGGCGACTGCCCGAGCCCCCCATCGCCCCGCCGCGCGCACAGCTCC GGCCAGCAGCTCCTTGGACAGGCGACTGCCCGTGCCCCCCATCGCCCCGCCGCGCGCACAGCTCC A T GDPGP1 Ensembl:ENSG00000183208 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:90233651..90234002;chr15:90233651..90233949;chr15:90233634..90234032;chr15:90233690..90234029;chr15:90233651..90234010 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs534664812 Functional Loss SNV dbSNP153 33..33 33 - - - 94954 RMVar_ID_94954 Human_SNP_ID_587255935 m1A Human chr15 + 90265728 90265728 90265728 GGCTGGTTTGCGTCGACATGGCGGTTACCCTGAGTCTCTTGCTGGGCGGGCGCGTTTGCGCCGCC GGCTGGTTTGCGTCGACATGGCGGTTACCCTGCGTCTCTTGCTGGGCGGGCGCGTTTGCGCCGCC A C NGRN,AC091167.2 Ensembl:ENSG00000182768,Ensembl:ENSG00000261147 Protein coding,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90265676..90265877 26863196 MeRIP-seq:(Medium) rs1012168362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814855,Human_RBP_ID_1002593,Human_RBP_ID_1510794,Human_RBP_ID_4342932,Human_RBP_ID_6479026,Human_RBP_ID_8425746,Human_RBP_ID_9057710,Human_RBP_ID_9324410,Human_RBP_ID_12634698,Human_RBP_ID_17119336,Human_RBP_ID_22047714,Human_RBP_ID_22439916,Human_RBP_ID_23674068 Human_miRNA_ID_2770934,Human_miRNA_ID_2770935 RMVar_hsa_circ_109702,RMVar_hsa_circ_111510,RMVar_hsa_circ_174752,RMVar_hsa_circ_127844,RMVar_hsa_circ_174753,RMVar_hsa_circ_116879,RMVar_hsa_circ_174754,RMVar_hsa_circ_174755 94955 RMVar_ID_94955 Human_SNP_ID_587256163 m1A Human chr15 - 90266209 90266209 90266209 GGATGTTTGAAGAGCCTCAGGCTAAATCATGGAGCGCCCAGCCCTCTTCTCTTTGATCGCAAGGG GGATGTTTGAAGAGCCTCAGGCTAAATCATGGCGCGCCCAGCCCTCTTCTCTTTGATCGCAAGGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90266026..90266300 32194978 MeRIP-seq:(Medium) rs1331067519 Functional Loss SNV dbSNP153 33..33 33 - - - 94956 RMVar_ID_94956 Human_SNP_ID_587257759 m1A Human chr15 - 90271662 90271662 90271662 AACTCCTCCAGCTTCTGACCACTTGGCAACGCACCACTGCCAGTTCCTCTGGGGCTCTCAGAATC AACTCCTCCAGCTTCTGACCACTTGGCAACGCTCCACTGCCAGTTCCTCTGGGGCTCTCAGAATC T A lnc-CIB1-3 RNACentral:URS00008B27EA lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90271345..90271794 26863196 MeRIP-seq:(Medium) rs370104771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174758 94957 RMVar_ID_94957 Human_SNP_ID_587305964 m1A Human chr15 + 90452811 90452811 90452811 GGCAGCAGTAGCACTGATTAATGCTGCAATCCAGAAGGGTGTTGCTGAGAAGACTGTTTTGGAAC GGCAGCAGTAGCACTGATTAATGCTGCAATCCGGAAGGGTGTTGCTGAGAAGACTGTTTTGGAAC A G IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90449629..90453154 32194978 MeRIP-seq:(Medium) rs754848833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1836906,Human_RBP_ID_5566818,Human_RBP_ID_8804168 Human_Splice_Rec_1644102,Human_Splice_Rec_1644176 Human_miRNA_ID_226782,Human_miRNA_ID_589636 RMVar_hsa_circ_915,RMVar_hsa_circ_80929,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_113637,RMVar_hsa_circ_174765,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_378533,RMVar_hsa_circ_174768,RMVar_hsa_circ_325516,RMVar_hsa_circ_174771,RMVar_hsa_circ_297589,RMVar_hsa_circ_341836,RMVar_hsa_circ_342091,RMVar_hsa_circ_118590,RMVar_hsa_circ_280892,RMVar_hsa_circ_126990,RMVar_hsa_circ_90363,RMVar_hsa_circ_96141,RMVar_hsa_circ_17611,RMVar_hsa_circ_7495,RMVar_hsa_circ_174780,RMVar_hsa_circ_127514,RMVar_hsa_circ_174775,RMVar_hsa_circ_174776,RMVar_hsa_circ_174773,RMVar_hsa_circ_174774,RMVar_hsa_circ_174772,RMVar_hsa_circ_105113,RMVar_hsa_circ_174781,RMVar_hsa_circ_80566,RMVar_hsa_circ_110777,RMVar_hsa_circ_368410,RMVar_hsa_circ_267221,RMVar_hsa_circ_96336,RMVar_hsa_circ_28117,RMVar_hsa_circ_30659,RMVar_hsa_circ_16052,RMVar_hsa_circ_87573,RMVar_hsa_circ_126002,RMVar_hsa_circ_174783,RMVar_hsa_circ_174784,RMVar_hsa_circ_174782,RMVar_hsa_circ_174789,RMVar_hsa_circ_72163,RMVar_hsa_circ_174790,RMVar_hsa_circ_22616,RMVar_hsa_circ_174792,RMVar_hsa_circ_64927,RMVar_hsa_circ_287317,RMVar_hsa_circ_336679,RMVar_hsa_circ_97147,RMVar_hsa_circ_25383,RMVar_hsa_circ_114764,RMVar_hsa_circ_174791,RMVar_hsa_circ_285127,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_174793 94958 RMVar_ID_94958 Human_SNP_ID_587309923 m1A Human chr15 + 90467591 90467591 90467591 AAATTCTATGCAGCTTTCTCGGGAGGAGATCCAGGTAGGTTACCTTTCTTCACGTAAGAAGAAGC AAATTCTATGCAGCTTTCTCGGGAGGAGATCCGGGTAGGTTACCTTTCTTCACGTAAGAAGAAGC A G IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90467561..90473059 32194978 MeRIP-seq:(Medium) rs372432449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2459518,Human_RBP_ID_8804178,Human_RBP_ID_9256540,Human_RBP_ID_9283797,Human_RBP_ID_17870603,Human_RBP_ID_19067603,Human_RBP_ID_22195672,Human_RBP_ID_22439918,Human_RBP_ID_22759483 Human_Splice_Rec_1644115,Human_Splice_Rec_1644189,Human_Splice_Rec_1644239,Human_Splice_Rec_1644295 RMVar_hsa_circ_80929,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_113637,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_174768,RMVar_hsa_circ_325516,RMVar_hsa_circ_174771,RMVar_hsa_circ_341836,RMVar_hsa_circ_118590,RMVar_hsa_circ_126990,RMVar_hsa_circ_96141,RMVar_hsa_circ_17611,RMVar_hsa_circ_7495,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174774,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_80566,RMVar_hsa_circ_110777,RMVar_hsa_circ_368410,RMVar_hsa_circ_267221,RMVar_hsa_circ_96336,RMVar_hsa_circ_28117,RMVar_hsa_circ_30659,RMVar_hsa_circ_16052,RMVar_hsa_circ_87573,RMVar_hsa_circ_174783,RMVar_hsa_circ_174784,RMVar_hsa_circ_174782,RMVar_hsa_circ_72163,RMVar_hsa_circ_174790,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_64927,RMVar_hsa_circ_336679,RMVar_hsa_circ_97147,RMVar_hsa_circ_25383,RMVar_hsa_circ_114764,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_79444,RMVar_hsa_circ_96288,RMVar_hsa_circ_118885,RMVar_hsa_circ_174796,RMVar_hsa_circ_174797,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_102052,RMVar_hsa_circ_174800,RMVar_hsa_circ_174802,RMVar_hsa_circ_86723,RMVar_hsa_circ_174803,RMVar_hsa_circ_174801,RMVar_hsa_circ_66609,RMVar_hsa_circ_286293,RMVar_hsa_circ_104056,RMVar_hsa_circ_174805,RMVar_hsa_circ_174806,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807 94959 RMVar_ID_94959 Human_SNP_ID_587309924 m1A Human chr15 + 90467591 90467591 90467591 AAATTCTATGCAGCTTTCTCGGGAGGAGATCCAGGTAGGTTACCTTTCTTCACGTAAGAAGAAGC AAATTCTATGCAGCTTTCTCGGGAGGAGATCCTGGTAGGTTACCTTTCTTCACGTAAGAAGAAGC A T IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90467561..90473059 32194978 MeRIP-seq:(Medium) rs372432449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2459518,Human_RBP_ID_8804178,Human_RBP_ID_9256540,Human_RBP_ID_9283797,Human_RBP_ID_17870603,Human_RBP_ID_19067603,Human_RBP_ID_22195672,Human_RBP_ID_22439918,Human_RBP_ID_22759483 Human_Splice_Rec_1644115,Human_Splice_Rec_1644189,Human_Splice_Rec_1644239,Human_Splice_Rec_1644295 RMVar_hsa_circ_80929,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_113637,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_174768,RMVar_hsa_circ_325516,RMVar_hsa_circ_174771,RMVar_hsa_circ_341836,RMVar_hsa_circ_118590,RMVar_hsa_circ_126990,RMVar_hsa_circ_96141,RMVar_hsa_circ_17611,RMVar_hsa_circ_7495,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174774,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_80566,RMVar_hsa_circ_110777,RMVar_hsa_circ_368410,RMVar_hsa_circ_267221,RMVar_hsa_circ_96336,RMVar_hsa_circ_28117,RMVar_hsa_circ_30659,RMVar_hsa_circ_16052,RMVar_hsa_circ_87573,RMVar_hsa_circ_174783,RMVar_hsa_circ_174784,RMVar_hsa_circ_174782,RMVar_hsa_circ_72163,RMVar_hsa_circ_174790,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_64927,RMVar_hsa_circ_336679,RMVar_hsa_circ_97147,RMVar_hsa_circ_25383,RMVar_hsa_circ_114764,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_79444,RMVar_hsa_circ_96288,RMVar_hsa_circ_118885,RMVar_hsa_circ_174796,RMVar_hsa_circ_174797,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_102052,RMVar_hsa_circ_174800,RMVar_hsa_circ_174802,RMVar_hsa_circ_86723,RMVar_hsa_circ_174803,RMVar_hsa_circ_174801,RMVar_hsa_circ_66609,RMVar_hsa_circ_286293,RMVar_hsa_circ_104056,RMVar_hsa_circ_174805,RMVar_hsa_circ_174806,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807 94960 RMVar_ID_94960 Human_SNP_ID_587311510 m1A Human chr15 + 90473797 90473797 90473797 TTACCTGCGCTCCCACAAAGATGAAGTTGTAAAGGTATGGTAGCCTGAACAGGGTTTCTCCATGA TTACCTGCGCTCCCACAAAGATGAAGTTGTAAGGGTATGGTAGCCTGAACAGGGTTTCTCCATGA A G IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90473776..90474073 32194978 MeRIP-seq:(Medium) rs755816222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1644118,Human_Splice_Rec_1644119,Human_Splice_Rec_1644192,Human_Splice_Rec_1644193,Human_Splice_Rec_1644242,Human_Splice_Rec_1644243 RMVar_hsa_circ_80929,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_113637,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_174768,RMVar_hsa_circ_341836,RMVar_hsa_circ_118590,RMVar_hsa_circ_126990,RMVar_hsa_circ_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174774,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_80566,RMVar_hsa_circ_110777,RMVar_hsa_circ_368410,RMVar_hsa_circ_96336,RMVar_hsa_circ_28117,RMVar_hsa_circ_30659,RMVar_hsa_circ_16052,RMVar_hsa_circ_87573,RMVar_hsa_circ_174783,RMVar_hsa_circ_174784,RMVar_hsa_circ_174782,RMVar_hsa_circ_174790,RMVar_hsa_circ_20848,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_64927,RMVar_hsa_circ_97147,RMVar_hsa_circ_25383,RMVar_hsa_circ_114764,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_79444,RMVar_hsa_circ_96288,RMVar_hsa_circ_118885,RMVar_hsa_circ_174796,RMVar_hsa_circ_174797,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_102052,RMVar_hsa_circ_174800,RMVar_hsa_circ_174802,RMVar_hsa_circ_86723,RMVar_hsa_circ_174803,RMVar_hsa_circ_174801,RMVar_hsa_circ_66609,RMVar_hsa_circ_104056,RMVar_hsa_circ_174806,RMVar_hsa_circ_124236,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807,RMVar_hsa_circ_32636,RMVar_hsa_circ_27438,RMVar_hsa_circ_88952,RMVar_hsa_circ_120510,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_174810,RMVar_hsa_circ_174811,RMVar_hsa_circ_174812,RMVar_hsa_circ_174809 94961 RMVar_ID_94961 Human_SNP_ID_587311512 m1A Human chr15 - 90473805 90473805 90473805 TGTGCCCCTCATGGAGAAACCCTGTTCAGGCTACCATACCTTTACAACTTCATCTTTGTGGGAGC TGTGCCCCTCATGGAGAAACCCTGTTCAGGCTGCCATACCTTTACAACTTCATCTTTGTGGGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90473803..90473882 26863196 MeRIP-seq:(Medium) rs918569771 Functional Loss SNV dbSNP153 33..33 33 - - - 94962 RMVar_ID_94962 Human_SNP_ID_587314894 m1A Human chr15 - 90486055 90486055 90486055 GTTCGTGGATTGGATCATTGTGCTCCGGAGCAATGGCATCCTGGTGATCCAACAGGAGCTGCAAA GTTCGTGGATTGGATCATTGTGCTCCGGAGCAGTGGCATCCTGGTGATCCAACAGGAGCTGCAAA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:90486026..90486075 26863196 MeRIP-seq:(Medium) rs535698281 Functional Loss SNV dbSNP153 33..33 33 - - - 94963 RMVar_ID_94963 Human_SNP_ID_587314913 m1A Human chr15 + 90486117 90486117 90486117 AACTGCTGGACGACCTCGGCGAGGTGCCCACCATCGAGTCCCTGATAGGTAGAGTTCTAACTTTT AACTGCTGGACGACCTCGGCGAGGTGCCCACCGTCGAGTCCCTGATAGGTAGAGTTCTAACTTTT A G IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:90486026..90486213 26863196 MeRIP-seq:(Medium) rs753502137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8804196,Human_RBP_ID_9256558,Human_RBP_ID_9283815,Human_RBP_ID_17367007,Human_RBP_ID_18671607,Human_RBP_ID_22439924,Human_RBP_ID_22759484 Human_Splice_Rec_1644140,Human_Splice_Rec_1644141,Human_Splice_Rec_1644216,Human_Splice_Rec_1644217,Human_Splice_Rec_1644264,Human_Splice_Rec_1644265,Human_Splice_Rec_1644308,Human_Splice_Rec_1644310,Human_Splice_Rec_1644311 Human_miRNA_ID_2873726,Human_miRNA_ID_2873727,Human_miRNA_ID_2981689,Human_miRNA_ID_2981690 RMVar_hsa_circ_10061,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_92142,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_341836,RMVar_hsa_circ_118590,RMVar_hsa_circ_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_368410,RMVar_hsa_circ_96336,RMVar_hsa_circ_87573,RMVar_hsa_circ_174782,RMVar_hsa_circ_174790,RMVar_hsa_circ_20848,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_97147,RMVar_hsa_circ_114764,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_79444,RMVar_hsa_circ_96288,RMVar_hsa_circ_174796,RMVar_hsa_circ_174797,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_174802,RMVar_hsa_circ_86723,RMVar_hsa_circ_174803,RMVar_hsa_circ_66609,RMVar_hsa_circ_104056,RMVar_hsa_circ_174806,RMVar_hsa_circ_124236,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_106849,RMVar_hsa_circ_174812,RMVar_hsa_circ_174813,RMVar_hsa_circ_84291,RMVar_hsa_circ_174816,RMVar_hsa_circ_56066,RMVar_hsa_circ_96155,RMVar_hsa_circ_174819,RMVar_hsa_circ_101774,RMVar_hsa_circ_105439,RMVar_hsa_circ_174818,RMVar_hsa_circ_312268,RMVar_hsa_circ_125928,RMVar_hsa_circ_174820,RMVar_hsa_circ_44075,RMVar_hsa_circ_174821,RMVar_hsa_circ_77141,RMVar_hsa_circ_117130,RMVar_hsa_circ_174822,RMVar_hsa_circ_174825,RMVar_hsa_circ_128212,RMVar_hsa_circ_280143,RMVar_hsa_circ_174823,RMVar_hsa_circ_346312,RMVar_hsa_circ_272151,RMVar_hsa_circ_174826,RMVar_hsa_circ_174824 94964 RMVar_ID_94964 Human_SNP_ID_587314914 m1A Human chr15 + 90486117 90486117 90486117 AACTGCTGGACGACCTCGGCGAGGTGCCCACCATCGAGTCCCTGATAGGTAGAGTTCTAACTTTT AACTGCTGGACGACCTCGGCGAGGTGCCCACCTTCGAGTCCCTGATAGGTAGAGTTCTAACTTTT A T IQGAP1 Ensembl:ENSG00000140575 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:90486026..90486213 26863196 MeRIP-seq:(Medium) rs753502137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8804196,Human_RBP_ID_9256558,Human_RBP_ID_9283815,Human_RBP_ID_17367007,Human_RBP_ID_18671607,Human_RBP_ID_22439924,Human_RBP_ID_22759484 Human_Splice_Rec_1644140,Human_Splice_Rec_1644141,Human_Splice_Rec_1644216,Human_Splice_Rec_1644217,Human_Splice_Rec_1644264,Human_Splice_Rec_1644265,Human_Splice_Rec_1644308,Human_Splice_Rec_1644310,Human_Splice_Rec_1644311 Human_miRNA_ID_2873726,Human_miRNA_ID_2873727,Human_miRNA_ID_2981689,Human_miRNA_ID_2981690 RMVar_hsa_circ_10061,RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,RMVar_hsa_circ_92142,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_341836,RMVar_hsa_circ_118590,RMVar_hsa_circ_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_368410,RMVar_hsa_circ_96336,RMVar_hsa_circ_87573,RMVar_hsa_circ_174782,RMVar_hsa_circ_174790,RMVar_hsa_circ_20848,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_97147,RMVar_hsa_circ_114764,RMVar_hsa_circ_88988,RMVar_hsa_circ_174794,RMVar_hsa_circ_174795,RMVar_hsa_circ_79444,RMVar_hsa_circ_96288,RMVar_hsa_circ_174796,RMVar_hsa_circ_174797,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_174802,RMVar_hsa_circ_86723,RMVar_hsa_circ_174803,RMVar_hsa_circ_66609,RMVar_hsa_circ_104056,RMVar_hsa_circ_174806,RMVar_hsa_circ_124236,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_106849,RMVar_hsa_circ_174812,RMVar_hsa_circ_174813,RMVar_hsa_circ_84291,RMVar_hsa_circ_174816,RMVar_hsa_circ_56066,RMVar_hsa_circ_96155,RMVar_hsa_circ_174819,RMVar_hsa_circ_101774,RMVar_hsa_circ_105439,RMVar_hsa_circ_174818,RMVar_hsa_circ_312268,RMVar_hsa_circ_125928,RMVar_hsa_circ_174820,RMVar_hsa_circ_44075,RMVar_hsa_circ_174821,RMVar_hsa_circ_77141,RMVar_hsa_circ_117130,RMVar_hsa_circ_174822,RMVar_hsa_circ_174825,RMVar_hsa_circ_128212,RMVar_hsa_circ_280143,RMVar_hsa_circ_174823,RMVar_hsa_circ_346312,RMVar_hsa_circ_272151,RMVar_hsa_circ_174826,RMVar_hsa_circ_174824 94965 RMVar_ID_94965 Human_SNP_ID_587316726 m1A Human chr15 + 90492505 90492505 90492505 ATTGCTGGGTTGTAGTGTGAAATGATAATGATAACTGTCGTTATTTTTCTAACTTTAATAATTAT ATTGCTGGGTTGTAGTGTGAAATGATAATGATGACTGTCGTTATTTTTCTAACTTTAATAATTAT A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90492502..90492613 26863196 MeRIP-seq:(Medium) rs1013025584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10061,RMVar_hsa_circ_92142,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_118590,RMVar_hsa_circ_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,RMVar_hsa_circ_174772,RMVar_hsa_circ_174781,RMVar_hsa_circ_96336,RMVar_hsa_circ_87573,RMVar_hsa_circ_174782,RMVar_hsa_circ_174790,RMVar_hsa_circ_20848,RMVar_hsa_circ_77530,RMVar_hsa_circ_174792,RMVar_hsa_circ_97147,RMVar_hsa_circ_114764,RMVar_hsa_circ_174795,RMVar_hsa_circ_96288,RMVar_hsa_circ_174796,RMVar_hsa_circ_97041,RMVar_hsa_circ_174799,RMVar_hsa_circ_174803,RMVar_hsa_circ_104056,RMVar_hsa_circ_174806,RMVar_hsa_circ_124236,RMVar_hsa_circ_100289,RMVar_hsa_circ_174807,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_106849,RMVar_hsa_circ_174812,RMVar_hsa_circ_174813,RMVar_hsa_circ_84291,RMVar_hsa_circ_174816,RMVar_hsa_circ_96155,RMVar_hsa_circ_174819,RMVar_hsa_circ_101774,RMVar_hsa_circ_105439,RMVar_hsa_circ_174818,RMVar_hsa_circ_174821,RMVar_hsa_circ_77141,RMVar_hsa_circ_117130,RMVar_hsa_circ_174822,RMVar_hsa_circ_29931,RMVar_hsa_circ_174825,RMVar_hsa_circ_128212,RMVar_hsa_circ_280143,RMVar_hsa_circ_174823,RMVar_hsa_circ_174826,RMVar_hsa_circ_272795,RMVar_hsa_circ_174828,RMVar_hsa_circ_81281,RMVar_hsa_circ_90816,RMVar_hsa_circ_174827,RMVar_hsa_circ_355010,RMVar_hsa_circ_113201,RMVar_hsa_circ_174832,RMVar_hsa_circ_295114,RMVar_hsa_circ_174833,RMVar_hsa_circ_174834 94966 RMVar_ID_94966 Human_SNP_ID_587327000 m1A Human chr15 + 90530021 90530021 90530021 GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTACAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTGCAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC A G CRTC3 Ensembl:ENSG00000140577 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:90529901..90530175 26863196 MeRIP-seq:(Medium) rs910957497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4340052,Human_RBP_ID_17367011 94967 RMVar_ID_94967 Human_SNP_ID_587327001 m1A Human chr15 + 90530021 90530021 90530021 GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTACAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTTCAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC A T CRTC3 Ensembl:ENSG00000140577 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:90529901..90530175 26863196 MeRIP-seq:(Medium) rs910957497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4340052,Human_RBP_ID_17367011 94968 RMVar_ID_94968 Human_SNP_ID_587327263 m1A Human chr15 + 90530726 90530726 90530726 CCGGCCCTGGGGTGGCTCGGGTTGTTGGAACCACGACGGGATTCCGTGTCGAGTGTGAGGCTCTG CCGGCCCTGGGGTGGCTCGGGTTGTTGGAACCGCGACGGGATTCCGTGTCGAGTGTGAGGCTCTG A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90530722..90530869 32194978 MeRIP-seq:(Medium) rs1039022197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1644401 94969 RMVar_ID_94969 Human_SNP_ID_587327294 m1A Human chr15 + 90530884 90530884 90530884 GGAGAGGGACCTGGAGGAATGAGTAAGGCGCGAGCCGGGACAAACACCTGGAGAGGTTAGGTAAC GGAGAGGGACCTGGAGGAATGAGTAAGGCGCGGGCCGGGACAAACACCTGGAGAGGTTAGGTAAC A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:90530850..90530982 26863196 MeRIP-seq:(Medium) rs1438844453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355339 94970 RMVar_ID_94970 Human_SNP_ID_587327722 m1A Human chr15 + 90532750 90532750 90532750 AAGCAGTGGGAAAATTTTGAGAAGGGAGTACTAGGAGGAGGAGTTGAGTGGTGGTACCTGGAATG AAGCAGTGGGAAAATTTTGAGAAGGGAGTACTGGGAGGAGGAGTTGAGTGGTGGTACCTGGAATG A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90532747..90532832 26863196 MeRIP-seq:(Medium) rs903687091 Functional Loss SNV dbSNP153 33..33 33 - - - 94971 RMVar_ID_94971 Human_SNP_ID_587328132 m1A Human chr15 + 90533917 90533917 90533917 GGGAGGGAATATGTTGCAGGTACAGAGAACAGAGATTCAGTAAAAGAGGATGAGGAGGGGATGTG GGGAGGGAATATGTTGCAGGTACAGAGAACAGTGATTCAGTAAAAGAGGATGAGGAGGGGATGTG A T CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90533913..90533984 26863196 MeRIP-seq:(Medium) rs966881427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12635786 94972 RMVar_ID_94972 Human_SNP_ID_587345035 m1A Human chr15 + 90600888 90600888 90600888 CAAAAGGAATGGGCTTGGTTTGGGTGAGTGATAAGGAGGCAACCTTCCACATAGGAGGTGAGAAA CAAAAGGAATGGGCTTGGTTTGGGTGAGTGATGAGGAGGCAACCTTCCACATAGGAGGTGAGAAA A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90600886..90600981 26863196 MeRIP-seq:(Medium) rs986292870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2460025,Human_RBP_ID_6479620,Human_RBP_ID_22933803 RMVar_hsa_circ_17814,RMVar_hsa_circ_174838,RMVar_hsa_circ_75563,RMVar_hsa_circ_307272,RMVar_hsa_circ_350127,RMVar_hsa_circ_115476,RMVar_hsa_circ_174839,RMVar_hsa_circ_271402,RMVar_hsa_circ_333091,RMVar_hsa_circ_377347,RMVar_hsa_circ_289115,RMVar_hsa_circ_64728,RMVar_hsa_circ_174840,RMVar_hsa_circ_174841,RMVar_hsa_circ_174842,RMVar_hsa_circ_21283,RMVar_hsa_circ_353353 94973 RMVar_ID_94973 Human_SNP_ID_587347785 m1A Human chr15 + 90611044 90611044 90611044 CTGCAGAGTTAAGGAGAAGGTTTACAATGCAAAGAACCTTGAAAGATGTAAGCCTGTTAATTGCA CTGCAGAGTTAAGGAGAAGGTTTACAATGCAAGGAACCTTGAAAGATGTAAGCCTGTTAATTGCA A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90611027..90611192 26863196 MeRIP-seq:(Medium) rs1295513239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12637032 RMVar_hsa_circ_17814,RMVar_hsa_circ_174838,RMVar_hsa_circ_75563,RMVar_hsa_circ_115476,RMVar_hsa_circ_174839,RMVar_hsa_circ_333091,RMVar_hsa_circ_377347,RMVar_hsa_circ_64728,RMVar_hsa_circ_174842,RMVar_hsa_circ_353353,RMVar_hsa_circ_107780,RMVar_hsa_circ_278297,RMVar_hsa_circ_363662,RMVar_hsa_circ_333825,RMVar_hsa_circ_266129,RMVar_hsa_circ_97706,RMVar_hsa_circ_174846,RMVar_hsa_circ_174847,RMVar_hsa_circ_174845,RMVar_hsa_circ_174849,RMVar_hsa_circ_118064,RMVar_hsa_circ_333159,RMVar_hsa_circ_174848 94974 RMVar_ID_94974 Human_SNP_ID_587352655 m1A Human chr15 - 90629340 90629340 90629340 AGGGAAAACAGACGGAGCGAAGGGTGAAGAGCAGATGCGTTGGGAACAGATGTCTGTGGGTGGTT AGGGAAAACAGACGGAGCGAAGGGTGAAGAGCGGATGCGTTGGGAACAGATGTCTGTGGGTGGTT T C CRTC3-AS1 Ensembl:ENSG00000259736 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90629291..90629493 26863196 MeRIP-seq:(Medium) rs774595088 Functional Loss SNV dbSNP153 33..33 33 - - - 94975 RMVar_ID_94975 Human_SNP_ID_587355564 m1A Human chr15 + 90638601 90638601 90638601 GCCCCTGAGGCCCCTGCCCAGCAGCCCCAGGCAGCCTCCTCACTGCCACAGTCAGACTTTCAGCT GCCCCTGAGGCCCCTGCCCAGCAGCCCCAGGCGGCCTCCTCACTGCCACAGTCAGACTTTCAGCT A G CRTC3 Ensembl:ENSG00000140577 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:90638501..90638650 26863410 MeRIP-seq:(Medium) rs548542658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17367125,Human_RBP_ID_27438173 Human_Splice_Rec_1644361,Human_Splice_Rec_1644387 Human_miRNA_ID_2457873,Human_miRNA_ID_2462796,Human_miRNA_ID_2635438,Human_miRNA_ID_2638125,Human_miRNA_ID_2715365,Human_miRNA_ID_3051343 RMVar_hsa_circ_377347,RMVar_hsa_circ_64728,RMVar_hsa_circ_174842,RMVar_hsa_circ_107780,RMVar_hsa_circ_97706,RMVar_hsa_circ_174846,RMVar_hsa_circ_174847,RMVar_hsa_circ_110712,RMVar_hsa_circ_174854,RMVar_hsa_circ_115460,RMVar_hsa_circ_174857,RMVar_hsa_circ_174858,RMVar_hsa_circ_277051,RMVar_hsa_circ_341753 94976 RMVar_ID_94976 Human_SNP_ID_587357032 m1A Human chr15 - 90642941 90642941 90642941 GGGAGGTCTGTGCTTGTCTGGAGTTTGTCTGGAGGCCACTGAGTATGAGACACCTGCAGTCCCTG GGGAGGTCTGTGCTTGTCTGGAGTTTGTCTGGGGGCCACTGAGTATGAGACACCTGCAGTCCCTG T C CRTC3-AS1 Ensembl:ENSG00000259736 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90642891..90642986 26863196 MeRIP-seq:(Medium) rs1406498619 Functional Loss SNV dbSNP153 33..33 33 - - - 94977 RMVar_ID_94977 Human_SNP_ID_587357320 m1A Human chr15 + 90643753 90643753 90643753 CAGGGGGAGGGGGGGGTCTAGGCTGTGAGAGGACAGGGTGGAGAGGAGGAGAACCCTGAAGGAGA CAGGGGGAGGGGGGGGTCTAGGCTGTGAGAGGGCAGGGTGGAGAGGAGGAGAACCCTGAAGGAGA A G CRTC3 Ensembl:ENSG00000140577 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90643707..90643840 26863196 MeRIP-seq:(Medium) rs1003159763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25178919,Human_RBP_ID_26438399 RMVar_hsa_circ_377347,RMVar_hsa_circ_174842,RMVar_hsa_circ_110712,RMVar_hsa_circ_174854 94978 RMVar_ID_94978 Human_SNP_ID_587418798 m1A Human chr15 + 90875634 90875634 90875634 CCGAGCCCTGCCCGTCTCGGCCCCATGCCCCCACCAGTCAGCCCCGGGCCACAGGCAGTGAGCAG CCGAGCCCTGCCCGTCTCGGCCCCATGCCCCCGCCAGTCAGCCCCGGGCCACAGGCAGTGAGCAG A G FURIN Ensembl:ENSG00000140564 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr15:90875552..90875853;chr15:90875519..90875771 26863196 MeRIP-seq:(Medium) rs1047174537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815055,Human_RBP_ID_4342474,Human_RBP_ID_5354226,Human_RBP_ID_18189611,Human_RBP_ID_22650261 Human_Splice_Rec_1644726,Human_Splice_Rec_1644756,Human_Splice_Rec_1644786,Human_Splice_Rec_1644790 RMVar_hsa_circ_114360,RMVar_hsa_circ_105692,RMVar_hsa_circ_346250,RMVar_hsa_circ_174865,RMVar_hsa_circ_127353,RMVar_hsa_circ_174866,RMVar_hsa_circ_174867 94979 RMVar_ID_94979 Human_SNP_ID_587418808 m1A Human chr15 + 90875691 90875663 90875692 GTGAGCAGGCACCTGGGAGCCGAGGCCCTGTGACCAGGCCAAGGAGACGGGCGCTCCAGGGTCCC GTGAG_____________________________CAGGCCAAGGAGACGGGCGCTCCAGGGTCCC GCAGGCACCTGGGAGCCGAGGCCCTGTGAC G FURIN Ensembl:ENSG00000140564 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:90875594..90875711;chr15:90875552..90875735 26863196 MeRIP-seq:(Medium) rs1241880150 Functional Loss DEL dbSNP153 6..34 33 - - - Human_RBP_ID_232242,Human_RBP_ID_4342475,Human_RBP_ID_18189613 Human_miRNA_ID_2218315,Human_miRNA_ID_2778058 RMVar_hsa_circ_114360,RMVar_hsa_circ_105692,RMVar_hsa_circ_346250,RMVar_hsa_circ_174865,RMVar_hsa_circ_127353,RMVar_hsa_circ_174866,RMVar_hsa_circ_174867 94980 RMVar_ID_94980 Human_SNP_ID_587418831 m1A Human chr15 + 90875716 90875716 90875716 CCCTGTGACCAGGCCAAGGAGACGGGCGCTCCAGGGTCCCAGCCACCTGTCCCCCCCATGGAGCT CCCTGTGACCAGGCCAAGGAGACGGGCGCTCCGGGGTCCCAGCCACCTGTCCCCCCCATGGAGCT A G FURIN Ensembl:ENSG00000140564 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:90875614..90875800 26863196 MeRIP-seq:(Medium) rs890087717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232242,Human_RBP_ID_4342475,Human_RBP_ID_18189614 Human_miRNA_ID_2890812 RMVar_hsa_circ_114360,RMVar_hsa_circ_105692,RMVar_hsa_circ_346250,RMVar_hsa_circ_174865,RMVar_hsa_circ_127353,RMVar_hsa_circ_174866,RMVar_hsa_circ_174867 94981 RMVar_ID_94981 Human_SNP_ID_587418862 m1A Human chr15 - 90875796 90875796 90875796 AGACCTTCTGGCCCTGAGCATCAGCTGCTAGCAGGACCAAGGTTCCTGTTGCTGCTACCACCCAT AGACCTTCTGGCCCTGAGCATCAGCTGCTAGCGGGACCAAGGTTCCTGTTGCTGCTACCACCCAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:90875776..90875800 26863196 MeRIP-seq:(Medium) rs763749238 Functional Loss SNV dbSNP153 33..33 33 - - - 94982 RMVar_ID_94982 Human_SNP_ID_587419721 m1A Human chr15 + 90878098 90878098 90878098 TGGGGTGGGGGCCCTGACAGCTGGACCCATGCAGCATCCCTCTTCGTGCCCCCCCTTCACGGCCA TGGGGTGGGGGCCCTGACAGCTGGACCCATGCGGCATCCCTCTTCGTGCCCCCCCTTCACGGCCA A G FURIN Ensembl:ENSG00000140564 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90878096..90878314 26863196 MeRIP-seq:(Medium) rs1567083593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887302,Human_RBP_ID_22650268,Human_RBP_ID_26779036 RMVar_hsa_circ_114360,RMVar_hsa_circ_105692,RMVar_hsa_circ_346250,RMVar_hsa_circ_174865,RMVar_hsa_circ_127353,RMVar_hsa_circ_95275,RMVar_hsa_circ_174866,RMVar_hsa_circ_174867,RMVar_hsa_circ_174868,RMVar_hsa_circ_110600,RMVar_hsa_circ_174869 94983 RMVar_ID_94983 Human_SNP_ID_587421030 m1A Human chr15 + 90881626 90881626 90881626 GGGCAACGGCTGCGGGCAGGGCTGCTGCCCTCACACCTGCCTGAGGTGGTGGCCGGCCTCAGCTG GGGCAACGGCTGCGGGCAGGGCTGCTGCCCTCGCACCTGCCTGAGGTGGTGGCCGGCCTCAGCTG A G FURIN Ensembl:ENSG00000140564 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:90881576..90881675 26863196 MeRIP-seq:(Medium) rs376540057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4340339,Human_RBP_ID_22047729,Human_RBP_ID_27438246 RMVar_hsa_circ_99850,RMVar_hsa_circ_105692,RMVar_hsa_circ_174865,RMVar_hsa_circ_127353,RMVar_hsa_circ_174867,RMVar_hsa_circ_174868,RMVar_hsa_circ_110600,RMVar_hsa_circ_104780,RMVar_hsa_circ_174870,RMVar_hsa_circ_174871,RMVar_hsa_circ_115851,RMVar_hsa_circ_79171,RMVar_hsa_circ_174873,RMVar_hsa_circ_174874 94984 RMVar_ID_94984 Human_SNP_ID_587429989 m1A Human chr15 + 90909348 90909348 90909348 TCCTGCCCCAGGGCAGCCCTGCTTCTGGACCAATACCGGAAGAAGTCCCAGCTGTTCCGAAGCAA TCCTGCCCCAGGGCAGCCCTGCTTCTGGACCAGTACCGGAAGAAGTCCCAGCTGTTCCGAAGCAA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs866654925 Functional Loss SNV dbSNP153 33..33 33 - - - 94985 RMVar_ID_94985 Human_SNP_ID_587432359 m1A Human chr15 - 90916265 90916246 90916266 TAGCCAGACCTGGCTCCCTGGGCGTCAGCCCCAGATGTTACCTCACTGCCCACGGTTCGCCGCTC TAGCCAGACCTGGCTCCCTGGGCGTCAGCCC____________________ACGGTTCGCCGCTC TGGGCAGTGAGGTAACATCTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90916263..90916368 26863196 MeRIP-seq:(Medium) rs1261829092 Functional Loss DEL dbSNP153 32..51 33 - - - 94986 RMVar_ID_94986 Human_SNP_ID_587433384 m1A Human chr15 + 90919725 90919725 90919725 TGACGTTACTGTACCCTCTGGCCTCCCCGTCCAACAGCACTGACGTCTATTTGGAGCCCATGGAG TGACGTTACTGTACCCTCTGGCCTCCCCGTCCGACAGCACTGACGTCTATTTGGAGCCCATGGAG A G MAN2A2 Ensembl:ENSG00000196547 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90919675..90919839 26863196 MeRIP-seq:(Medium) rs1183691302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758743,Human_RBP_ID_18189644,Human_RBP_ID_18671823,Human_RBP_ID_22581362 Human_Splice_Rec_1645156,Human_Splice_Rec_1645198,Human_Splice_Rec_1645238,Human_Splice_Rec_1645302,Human_Splice_Rec_1645348,Human_Splice_Rec_1645404,Human_Splice_Rec_1645426,Human_Splice_Rec_1645434,Human_Splice_Rec_1645440,Human_Splice_Rec_1645446,Human_Splice_Rec_1645454,Human_Splice_Rec_1645460,Human_Splice_Rec_1645462 Human_miRNA_ID_423422,Human_miRNA_ID_1511372,Human_miRNA_ID_2350568,Human_miRNA_ID_2775282 RMVar_hsa_circ_127370,RMVar_hsa_circ_174880 94987 RMVar_ID_94987 Human_SNP_ID_587436700 m1A Human chr15 - 90932112 90932112 90932112 CGACCTGACTTCCTGCTTTGCCCCTCCCCGTCAGGTGTGGCACGGATCCTGACCCACGAGGCGGG CGACCTGACTTCCTGCTTTGCCCCTCCCCGTCGGGTGTGGCACGGATCCTGACCCACGAGGCGGG T C HDDC3 Ensembl:ENSG00000184508 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:90932051..90932125 26863410 MeRIP-seq:(Medium) rs368111215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4340550,Human_RBP_ID_5236300,Human_RBP_ID_22650472 Human_Splice_Rec_1645467,Human_Splice_Rec_1645471,Human_Splice_Rec_1645479,Human_Splice_Rec_1645485,Human_Splice_Rec_1645489,Human_Splice_Rec_1645495,Human_Splice_Rec_1645501 RMVar_hsa_circ_81800,RMVar_hsa_circ_174883 94988 RMVar_ID_94988 Human_SNP_ID_587436815 m1A Human chr15 - 90932476 90932476 90932476 TGCCGACTTCGCGGCTCGCAAGCACCGGCAGCAGCGGCGGAAGGACCCCGAGGGGACCCCCTACA TGCCGACTTCGCGGCTCGCAAGCACCGGCAGCCGCGGCGGAAGGACCCCGAGGGGACCCCCTACA T G HDDC3 Ensembl:ENSG00000184508 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:90932426..90932575 26863410 MeRIP-seq:(Medium) rs1233238066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342942,Human_RBP_ID_22934738 Human_Splice_Rec_1645465,Human_Splice_Rec_1645477,Human_Splice_Rec_1645483,Human_Splice_Rec_1645493,Human_Splice_Rec_1645499 RMVar_hsa_circ_81800,RMVar_hsa_circ_174883 94989 RMVar_ID_94989 Human_SNP_ID_587439692 m1A Human chr15 + 90942559 90942559 90942559 CTGCTGCAGGTTATGTTTGATGCCCTCAAGGAAGGTGTCAAAAAAGGCTTCCGAGGCAAAGAAGG CTGCTGCAGGTTATGTTTGATGCCCTCAAGGAGGGTGTCAAAAAAGGCTTCCGAGGCAAAGAAGG A G UNC45A Ensembl:ENSG00000140553 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90942461..90942612 32194978 MeRIP-seq:(Medium) rs200987825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1645541,Human_Splice_Rec_1645585,Human_Splice_Rec_1645629,Human_Splice_Rec_1645703 RMVar_hsa_circ_112478,RMVar_hsa_circ_91863,RMVar_hsa_circ_107959,RMVar_hsa_circ_174885,RMVar_hsa_circ_174886,RMVar_hsa_circ_113551,RMVar_hsa_circ_174887,RMVar_hsa_circ_100469,RMVar_hsa_circ_76200,RMVar_hsa_circ_80040,RMVar_hsa_circ_174888,RMVar_hsa_circ_174889,RMVar_hsa_circ_57724,RMVar_hsa_circ_111051,RMVar_hsa_circ_116625,RMVar_hsa_circ_174890,RMVar_hsa_circ_174891,RMVar_hsa_circ_174892,RMVar_hsa_circ_174893,RMVar_hsa_circ_371801,RMVar_hsa_circ_78631,RMVar_hsa_circ_174894,RMVar_hsa_circ_174895,RMVar_hsa_circ_358258 94990 RMVar_ID_94990 Human_SNP_ID_587439749 m1A Human chr15 - 90942715 90942715 90942715 TAGAGTAAAATAATGTCACCAAACCGTATTCCAAACAACCTGCAGCTGCAAGTCTGGTCCCCAAA TAGAGTAAAATAATGTCACCAAACCGTATTCCTAACAACCTGCAGCTGCAAGTCTGGTCCCCAAA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90942711..90942862 32194978 MeRIP-seq:(Medium) rs944743001 Functional Loss SNV dbSNP153 33..33 33 - - - 94991 RMVar_ID_94991 Human_SNP_ID_587439851 m1A Human chr15 + 90943050 90943047 90943050 AGCGGTGCCCCGGAAGTCTCTCAAGGACCCCAACAACAGCCTCACCCTCTGGGTCATCGACCAAG AGCGGTGCCCCGGAAGTCTCTCAAGGACCC___CAACAGCCTCACCCTCTGGGTCATCGACCAAG CCAA C UNC45A Ensembl:ENSG00000140553 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90943001..90943050 32194978 MeRIP-seq:(Medium) rs1180464560 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_232239 Human_Splice_Rec_1645543,Human_Splice_Rec_1645587,Human_Splice_Rec_1645631,Human_Splice_Rec_1645705,Human_Splice_Rec_1645743 Human_miRNA_ID_189420,Human_miRNA_ID_2715369,Human_miRNA_ID_3051347 RMVar_hsa_circ_112478,RMVar_hsa_circ_107959,RMVar_hsa_circ_174885,RMVar_hsa_circ_174886,RMVar_hsa_circ_113551,RMVar_hsa_circ_100469,RMVar_hsa_circ_76200,RMVar_hsa_circ_80040,RMVar_hsa_circ_174888,RMVar_hsa_circ_174889,RMVar_hsa_circ_57724,RMVar_hsa_circ_116625,RMVar_hsa_circ_174891,RMVar_hsa_circ_174892,RMVar_hsa_circ_174893,RMVar_hsa_circ_371801,RMVar_hsa_circ_174896,RMVar_hsa_circ_123104,RMVar_hsa_circ_174895,RMVar_hsa_circ_125113,RMVar_hsa_circ_358258,RMVar_hsa_circ_174897 94992 RMVar_ID_94992 Human_SNP_ID_587441038 m1A Human chr15 + 90946733 90946733 90946733 CAACCGGGCCTTGGAGCTGAGCGGTGTCATGGAGAGTGTGATTGCTCTGTGTGCCTCTGAGCAGG CAACCGGGCCTTGGAGCTGAGCGGTGTCATGGCGAGTGTGATTGCTCTGTGTGCCTCTGAGCAGG A C UNC45A Ensembl:ENSG00000140553 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90946682..90946777 26863196 MeRIP-seq:(Medium) rs1160165327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8803977,Human_RBP_ID_9283831,Human_RBP_ID_22440501,Human_RBP_ID_23674536 RMVar_hsa_circ_112478,RMVar_hsa_circ_107959,RMVar_hsa_circ_174885,RMVar_hsa_circ_174886,RMVar_hsa_circ_113551,RMVar_hsa_circ_100469,RMVar_hsa_circ_76200,RMVar_hsa_circ_80040,RMVar_hsa_circ_174888,RMVar_hsa_circ_174889,RMVar_hsa_circ_116625,RMVar_hsa_circ_174891,RMVar_hsa_circ_174892,RMVar_hsa_circ_174896,RMVar_hsa_circ_123104,RMVar_hsa_circ_174895,RMVar_hsa_circ_125113,RMVar_hsa_circ_174897,RMVar_hsa_circ_174898,RMVar_hsa_circ_93289,RMVar_hsa_circ_174899,RMVar_hsa_circ_332197 94993 RMVar_ID_94993 Human_SNP_ID_587441549 m1A Human chr15 - 90948247 90948247 90948247 CTGAGCTGGAACAGAGCTTTCAGAGCAGCCGCATCCTCCACAAACTCTTCCTTCACGTCGGCATC CTGAGCTGGAACAGAGCTTTCAGAGCAGCCGCGTCCTCCACAAACTCTTCCTTCACGTCGGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90948201..90948300 26863196 MeRIP-seq:(Medium) rs111289397 Functional Loss SNV dbSNP153 33..33 33 - - - 94994 RMVar_ID_94994 Human_SNP_ID_587443311 m1A Human chr15 + 90953546 90953546 90953546 TGCAGCACCGGGGTGCTGTGGTGGTGCTGAACATGGTGGAGGCCTCGAGGGAGATTGCCAGCACC TGCAGCACCGGGGTGCTGTGGTGGTGCTGAACGTGGTGGAGGCCTCGAGGGAGATTGCCAGCACC A G UNC45A Ensembl:ENSG00000140553 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90950141..90953600 32194978 MeRIP-seq:(Medium) rs774212444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22440777 Human_Splice_Rec_1645566,Human_Splice_Rec_1645610,Human_Splice_Rec_1645654,Human_Splice_Rec_1645728,Human_Splice_Rec_1645766,Human_Splice_Rec_1645776 RMVar_hsa_circ_112478,RMVar_hsa_circ_107959,RMVar_hsa_circ_174885,RMVar_hsa_circ_174886,RMVar_hsa_circ_100469,RMVar_hsa_circ_113920,RMVar_hsa_circ_76200,RMVar_hsa_circ_174888,RMVar_hsa_circ_116625,RMVar_hsa_circ_174892,RMVar_hsa_circ_123104,RMVar_hsa_circ_174895,RMVar_hsa_circ_174897,RMVar_hsa_circ_174898,RMVar_hsa_circ_93289,RMVar_hsa_circ_95276,RMVar_hsa_circ_127340,RMVar_hsa_circ_116172,RMVar_hsa_circ_174901,RMVar_hsa_circ_174902,RMVar_hsa_circ_110885,RMVar_hsa_circ_174903,RMVar_hsa_circ_174904,RMVar_hsa_circ_124259,RMVar_hsa_circ_174905,RMVar_hsa_circ_174906 94995 RMVar_ID_94995 Human_SNP_ID_587443352 m1A Human chr15 - 90953691 90953691 90953691 AACCCCCTCACTCTCCATCTTGGTTGGGTTGGATAAGCCCATATTCCACTGCTTTGTCCAGGCAG AACCCCCTCACTCTCCATCTTGGTTGGGTTGGGTAAGCCCATATTCCACTGCTTTGTCCAGGCAG T C AC068831.2 Ensembl:ENSG00000258384 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:90953642..90954043 32194978 MeRIP-seq:(Medium) rs878942963 Functional Loss SNV dbSNP153 33..33 33 - - - 94996 RMVar_ID_94996 Human_SNP_ID_587443766 m1A Human chr15 - 90954950 90954950 90954950 GTGACGCCCAAGACGGGCGGACCCCGCCACCCACCTCAGTCCCGGGACCGCGGCAGCTCAAAACC GTGACGCCCAAGACGGGCGGACCCCGCCACCCCCCTCAGTCCCGGGACCGCGGCAGCTCAAAACC T G AC068831.2 Ensembl:ENSG00000258384 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90954909..90955700 26863196 MeRIP-seq:(Medium) rs1176164764 Functional Loss SNV dbSNP153 33..33 33 - - - 94997 RMVar_ID_94997 Human_SNP_ID_587443923 m1A Human chr15 - 90955399 90955396 90955399 TCTACCCTCTCGGGCAGGTCCTTCTGGTGGGCAGCCTTGGAGGAAACGCCGAGGCGCAGAGCGGC TCTACCCTCTCGGGCAGGTCCTTCTGGTGGGC___CTTGGAGGAAACGCCGAGGCGCAGAGCGGC GGCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:90955396..90955515 26863196 MeRIP-seq:(Medium) rs1458004199 Functional Loss DEL dbSNP153 33..35 33 - - - 94998 RMVar_ID_94998 Human_SNP_ID_587444897 m1A Human chr15 - 90957718 90957718 90957718 TCTGGAGAAGCACTAAGTCACTCACCACTCACACACACAGAATGCCAGCCCCCCGCGGCCACCTC TCTGGAGAAGCACTAAGTCACTCACCACTCACGCACACAGAATGCCAGCCCCCCGCGGCCACCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:90955804..90959796;chr15:90955848..90959796 26863196 MeRIP-seq:(Medium) rs779844641 Functional Loss SNV dbSNP153 33..33 33 - - - 94999 RMVar_ID_94999 Human_SNP_ID_587444898 m1A Human chr15 - 90957718 90957718 90957718 TCTGGAGAAGCACTAAGTCACTCACCACTCACACACACAGAATGCCAGCCCCCCGCGGCCACCTC TCTGGAGAAGCACTAAGTCACTCACCACTCACCCACACAGAATGCCAGCCCCCCGCGGCCACCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:90955804..90959796;chr15:90955848..90959796 26863196 MeRIP-seq:(Medium) rs779844641 Functional Loss SNV dbSNP153 33..33 33 - - - 95000 RMVar_ID_95000 Human_SNP_ID_587444903 m1A Human chr15 - 90957727 90957727 90957727 ATGAGCTCGTCTGGAGAAGCACTAAGTCACTCACCACTCACACACACAGAATGCCAGCCCCCCGC ATGAGCTCGTCTGGAGAAGCACTAAGTCACTCCCCACTCACACACACAGAATGCCAGCCCCCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:90956601..90959796;chr15:90955848..90959796 26863196 MeRIP-seq:(Medium) rs1184159556 Functional Loss SNV dbSNP153 33..33 33 - - - 95001 RMVar_ID_95001 Human_SNP_ID_587445806 m1A Human chr15 + 90960332 90960332 90960332 TGTTCACATCATTATTATCATTCTGAAGCCACAGAACTGAATGAAGATGGTTCTCAGGTGAAGAG TGTTCACATCATTATTATCATTCTGAAGCCACGGAACTGAATGAAGATGGTTCTCAGGTGAAGAG A G RCCD1 Ensembl:ENSG00000166965 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90960326..90960375 26863196 MeRIP-seq:(Medium) rs960968235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886032,Human_RBP_ID_3945915,Human_RBP_ID_18981839,Human_RBP_ID_26327069 Human_Splice_Rec_1645788,Human_Splice_Rec_1645816,Human_Splice_Rec_1645826,Human_Splice_Rec_1645842,Human_Splice_Rec_1645854 RMVar_hsa_circ_268618,RMVar_hsa_circ_278583,RMVar_hsa_circ_174907 95002 RMVar_ID_95002 Human_SNP_ID_587450765 m1A Human chr15 - 90974524 90974524 90974524 AAAAGACGAAGAAAGTAATCTGAGCAGCCCATAGTCTCTGCCGGGGACCAGGGTTTGTGGAACAG AAAAGACGAAGAAAGTAATCTGAGCAGCCCATGGTCTCTGCCGGGGACCAGGGTTTGTGGAACAG T C AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90974522..90974669 26863196 MeRIP-seq:(Medium) rs1233199729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355361 RMVar_hsa_circ_75163,RMVar_hsa_circ_49308,RMVar_hsa_circ_106428,RMVar_hsa_circ_114313,RMVar_hsa_circ_121413,RMVar_hsa_circ_109536,RMVar_hsa_circ_90798,RMVar_hsa_circ_174908,RMVar_hsa_circ_174910,RMVar_hsa_circ_174911,RMVar_hsa_circ_174912,RMVar_hsa_circ_174909,RMVar_hsa_circ_114358,RMVar_hsa_circ_116418,RMVar_hsa_circ_375970,RMVar_hsa_circ_99176,RMVar_hsa_circ_174915,RMVar_hsa_circ_174916,RMVar_hsa_circ_174917,RMVar_hsa_circ_174914,RMVar_hsa_circ_61093,RMVar_hsa_circ_104298,RMVar_hsa_circ_30689,RMVar_hsa_circ_370843,RMVar_hsa_circ_174918,RMVar_hsa_circ_174919,RMVar_hsa_circ_98695,RMVar_hsa_circ_174920,RMVar_hsa_circ_62368 95003 RMVar_ID_95003 Human_SNP_ID_587452570 m1A Human chr15 + 90980368 90980368 90980368 TTTCTTCATGTTTTGCATTTTCAGTTCTTCCAACCGATCCACTTCTAATTGCAGCTGAAAGAAAG TTTCTTCATGTTTTGCATTTTCAGTTCTTCCACCCGATCCACTTCTAATTGCAGCTGAAAGAAAG A C PRC1-AS1 Ensembl:ENSG00000258725 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90980317..90980418 26863196 MeRIP-seq:(Medium) rs746327520 Functional Loss SNV dbSNP153 33..33 33 - - - 95004 RMVar_ID_95004 Human_SNP_ID_587452792 m1A Human chr15 - 90980935 90980935 90980935 TGGGACAGGTTGCAAATACCTGAAGAAGAAAGAGAAGCTGTGGCCACCATTATGTCTGGGTCAAA TGGGACAGGTTGCAAATACCTGAAGAAGAAAGCGAAGCTGTGGCCACCATTATGTCTGGGTCAAA T G AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90980849..90980983 26863196 MeRIP-seq:(Medium) rs529948276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1511060,Human_RBP_ID_1837146,Human_RBP_ID_6480293,Human_RBP_ID_9371287,Human_RBP_ID_12639905,Human_RBP_ID_18283477,Human_RBP_ID_18529075,Human_RBP_ID_18671938,Human_RBP_ID_23674657,Human_RBP_ID_26327084,Human_RBP_ID_27810638 Human_Splice_Rec_1645870,Human_Splice_Rec_1645871,Human_Splice_Rec_1645902,Human_Splice_Rec_1645903,Human_Splice_Rec_1645944,Human_Splice_Rec_1645945,Human_Splice_Rec_1645981,Human_Splice_Rec_1645992,Human_Splice_Rec_1646000,Human_Splice_Rec_1646092,Human_Splice_Rec_1646093,Human_Splice_Rec_1646159 Human_miRNA_ID_2675594,Human_miRNA_ID_2926345,Human_miRNA_ID_3118427 RMVar_hsa_circ_49308,RMVar_hsa_circ_106428,RMVar_hsa_circ_109536,RMVar_hsa_circ_174908,RMVar_hsa_circ_174909,RMVar_hsa_circ_114358,RMVar_hsa_circ_116418,RMVar_hsa_circ_375970,RMVar_hsa_circ_174915,RMVar_hsa_circ_174916,RMVar_hsa_circ_174917,RMVar_hsa_circ_61093,RMVar_hsa_circ_98695,RMVar_hsa_circ_174920,RMVar_hsa_circ_62368,RMVar_hsa_circ_174921,RMVar_hsa_circ_81400,RMVar_hsa_circ_345530,RMVar_hsa_circ_314924,RMVar_hsa_circ_54339,RMVar_hsa_circ_115607,RMVar_hsa_circ_174922,RMVar_hsa_circ_174923,RMVar_hsa_circ_174924,RMVar_hsa_circ_317745 95005 RMVar_ID_95005 Human_SNP_ID_587452800 m1A Human chr15 + 90980969 90980969 90980969 TTTCTTCTTCAGGTATTTGCAACCTGTCCCAGAGCTCTCGGATTTGAGTACGCAGCCCCTCACAC TTTCTTCTTCAGGTATTTGCAACCTGTCCCAGGGCTCTCGGATTTGAGTACGCAGCCCCTCACAC A G PRC1-AS1 Ensembl:ENSG00000258725 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90980918..90981018 32194978 MeRIP-seq:(Medium) rs1441893021 Functional Loss SNV dbSNP153 33..33 33 - - - 95006 RMVar_ID_95006 Human_SNP_ID_587456551 m1A Human chr15 + 90994482 90994482 90994482 CCAGACCTACTCCACACGGCCCCGAGAGCAACAACCACCCGCAAACACCGGCGATGTCACTCCGC CCAGACCTACTCCACACGGCCCCGAGAGCAACCACCACCCGCAAACACCGGCGATGTCACTCCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:90994217..90994575;chr15:90994292..90994525;chr15:90994152..90994584;chr15:90994071..90994575;chr15:90994221..90994575 26863196 MeRIP-seq:(Medium) rs985873349 Functional Loss SNV dbSNP153 33..33 33 - - - 95007 RMVar_ID_95007 Human_SNP_ID_587528455 m1A Human chr15 - 91270904 91270902 91270904 GACTCACCGTCCTCCCATCGTCCACAGGACTCACCGTCCTCCCATCATCCACAAGATTCACCGTC GACTCACCGTCCTCCCATCGTCCACAGGACTC__CGTCCTCCCATCATCCACAAGATTCACCGTC GGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:91270854..91271139 26863196 MeRIP-seq:(Medium) rs1341224575 Functional Loss DEL dbSNP153 33..34 33 - - - 95008 RMVar_ID_95008 Human_SNP_ID_587682959 m1A Human chr15 + 91853876 91853873 91853876 GCCCCGACACCCGGGGCGAGCGGGAAAGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGGGGAAGG GCCCCGACACCCGGGGCGAGCGGGAAAGCG___GCGGCGGCGGCGGCGGCGGCGGCGGGGGAAGG GGCA G SLCO3A1 Ensembl:ENSG00000176463 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:91853352..91854127 26863196 MeRIP-seq:(Medium) rs758850577 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_174958,RMVar_hsa_circ_80571,RMVar_hsa_circ_174957 95009 RMVar_ID_95009 Human_SNP_ID_587682962 m1A Human chr15 + 91853876 91853876 91853876 GCCCCGACACCCGGGGCGAGCGGGAAAGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGGGGAAGG GCCCCGACACCCGGGGCGAGCGGGAAAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGAAGG A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:91853352..91854127 26863196 MeRIP-seq:(Medium) rs1215476541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_174958,RMVar_hsa_circ_80571,RMVar_hsa_circ_174957 95010 RMVar_ID_95010 Human_SNP_ID_587686311 m1A Human chr15 - 91866893 91866893 91866893 AAAATTATTTTATATCTCCGACCAGTCTACCCAGGCCCATCTCCCACCCTGGCCCAATGCTTTGC AAAATTATTTTATATCTCCGACCAGTCTACCCTGGCCCATCTCCCACCCTGGCCCAATGCTTTGC T A lnc-FAM174B-8 RNACentral:URS00008B4BE9 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:91866889..91867047 26863196 MeRIP-seq:(Medium) rs1421338557 Functional Loss SNV dbSNP153 33..33 33 - - - 95011 RMVar_ID_95011 Human_SNP_ID_587693381 m1A Human chr15 + 91894396 91894396 91894396 AATATCTAATTGCCATGTAGTGTGCATGGACAATGGGGAGAGGCATGGCAGGTGTGGTGGTATCT AATATCTAATTGCCATGTAGTGTGCATGGACATTGGGGAGAGGCATGGCAGGTGTGGTGGTATCT A T SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:91894395..91894570 26863196 MeRIP-seq:(Medium) rs1567174589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_80571,RMVar_hsa_circ_174957,RMVar_hsa_circ_174959 95012 RMVar_ID_95012 Human_SNP_ID_587698902 m1A Human chr15 + 91916323 91916323 91916323 GGCCCGACCCCGACCTCATCTGCCGCAACCGGACGGCTACCAACATGATGTACTTGCTGCTCATT GGCCCGACCCCGACCTCATCTGCCGCAACCGGCCGGCTACCAACATGATGTACTTGCTGCTCATT A C SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:91916276..91916350 26863196 MeRIP-seq:(Medium) rs759282606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27438321 RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_80571,RMVar_hsa_circ_174957,RMVar_hsa_circ_174959,RMVar_hsa_circ_302845,RMVar_hsa_circ_174960,RMVar_hsa_circ_174961 95013 RMVar_ID_95013 Human_SNP_ID_587698903 m1A Human chr15 + 91916323 91916323 91916323 GGCCCGACCCCGACCTCATCTGCCGCAACCGGACGGCTACCAACATGATGTACTTGCTGCTCATT GGCCCGACCCCGACCTCATCTGCCGCAACCGGGCGGCTACCAACATGATGTACTTGCTGCTCATT A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:91916276..91916350 26863196 MeRIP-seq:(Medium) rs759282606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27438321 RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_80571,RMVar_hsa_circ_174957,RMVar_hsa_circ_174959,RMVar_hsa_circ_302845,RMVar_hsa_circ_174960,RMVar_hsa_circ_174961 95014 RMVar_ID_95014 Human_SNP_ID_587707777 m1A Human chr15 + 91950304 91950304 91950304 GGGGATTGCAGGGGGCTGGGGAAGCAGAGATCAGTCTGCAGTGGTGGGTGAAGACAGCCAGTCGT GGGGATTGCAGGGGGCTGGGGAAGCAGAGATCGGTCTGCAGTGGTGGGTGAAGACAGCCAGTCGT A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:91950188..91950382 26863196 MeRIP-seq:(Medium) rs941624683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_174961 95015 RMVar_ID_95015 Human_SNP_ID_587730633 m1A Human chr15 + 92032637 92032637 92032637 GGGTAGTGGAGGTGCTCTCTGGGTTTTGGCAGAAAGCCCTGGGTGCGGTGATTGGGTAGGTTGGA GGGTAGTGGAGGTGCTCTCTGGGTTTTGGCAGGAAGCCCTGGGTGCGGTGATTGGGTAGGTTGGA A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:92032623..92032752 26863196 MeRIP-seq:(Medium) rs768233083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_174961 95016 RMVar_ID_95016 Human_SNP_ID_587730695 m1A Human chr15 + 92032770 92032770 92032770 GGAAAGCAGGCCAAGTTGGAGATGTGGTGAGGAGACAGCTTTGAGGAGCATCATGGAAGCAGTAC GGAAAGCAGGCCAAGTTGGAGATGTGGTGAGGGGACAGCTTTGAGGAGCATCATGGAAGCAGTAC A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:92032328..92032861 26863196 MeRIP-seq:(Medium) rs1013007321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_174961 95017 RMVar_ID_95017 Human_SNP_ID_587730983 m1A Human chr15 + 92033694 92033694 92033694 GTGAGGGAGAGAGACAGTAAACAATATAACTAAGAAGAGTAGGTGGTGGCTCGCTGGTGGCAAAA GTGAGGGAGAGAGACAGTAAACAATATAACTAGGAAGAGTAGGTGGTGGCTCGCTGGTGGCAAAA A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:92033676..92034599 26863196 MeRIP-seq:(Medium) rs1431263448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_174961 95018 RMVar_ID_95018 Human_SNP_ID_587750583 m1A Human chr15 + 92104435 92104435 92104435 CCCGCACTCAGAGCCCGCCATGGAAAGCGAGCAGGCCATGCTCTCCGAAAGAGAATACGAGAGAC CCCGCACTCAGAGCCCGCCATGGAAAGCGAGCGGGCCATGCTCTCCGAAAGAGAATACGAGAGAC A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92104332..92104518 26863196 MeRIP-seq:(Medium) rs1484885148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37228,RMVar_hsa_circ_122260,RMVar_hsa_circ_110046,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_174961,RMVar_hsa_circ_361576,RMVar_hsa_circ_370084,RMVar_hsa_circ_332542,RMVar_hsa_circ_174964,RMVar_hsa_circ_174965,RMVar_hsa_circ_348642 95019 RMVar_ID_95019 Human_SNP_ID_587756062 m1A Human chr15 + 92126126 92126126 92126126 TCTTCCTGGGAGGTCTTTTGGTGAAGAAGCTCAGCCTGTCTGCCCTGGGGGCCATTCGGATGGCC TCTTCCTGGGAGGTCTTTTGGTGAAGAAGCTCGGCCTGTCTGCCCTGGGGGCCATTCGGATGGCC A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:92126101..92126125 26863196 MeRIP-seq:(Medium) rs1325435651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20004668 Human_Splice_Rec_1646522,Human_Splice_Rec_1646540,Human_Splice_Rec_1646556,Human_Splice_Rec_1646582,Human_Splice_Rec_1646602 Human_miRNA_ID_2469444,Human_miRNA_ID_2469445 RMVar_hsa_circ_122260,RMVar_hsa_circ_101544,RMVar_hsa_circ_174958,RMVar_hsa_circ_174959,RMVar_hsa_circ_370084,RMVar_hsa_circ_332542,RMVar_hsa_circ_174967,RMVar_hsa_circ_174964,RMVar_hsa_circ_174965,RMVar_hsa_circ_85352,RMVar_hsa_circ_370325,RMVar_hsa_circ_348642,RMVar_hsa_circ_294242,RMVar_hsa_circ_174968,RMVar_hsa_circ_326339,RMVar_hsa_circ_174966 95020 RMVar_ID_95020 Human_SNP_ID_587764853 m1A Human chr15 + 92153850 92153850 92153850 CCCAGCATGTTTGGGGGCTGCAGAAGGCCCAGACTGGGGGGAAAGGGGGGACAGAAGAAGATGGA CCCAGCATGTTTGGGGGCTGCAGAAGGCCCAGGCTGGGGGGAAAGGGGGGACAGAAGAAGATGGA A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:92153654..92154126 26863196 MeRIP-seq:(Medium) rs529102003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 95021 RMVar_ID_95021 Human_SNP_ID_587765151 m1A Human chr15 + 92154819 92154819 92154819 GAGTGGAGCCAAAGAAGCTGAGGGTGATGATCAAAGTAGGGCTGAGATGGGAGAAAGGAGAGAGG GAGTGGAGCCAAAGAAGCTGAGGGTGATGATCGAAGTAGGGCTGAGATGGGAGAAAGGAGAGAGG A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:92154632..92154854 26863196 MeRIP-seq:(Medium) rs1321195772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 95022 RMVar_ID_95022 Human_SNP_ID_587767867 m1A Human chr15 + 92163334 92163334 92163334 AGCCAGACAGGATTCAGAATAAGGAGAGAATGACATCGTGCGGCAGGGTCCTGGAGGCCACTTGC AGCCAGACAGGATTCAGAATAAGGAGAGAATGGCATCGTGCGGCAGGGTCCTGGAGGCCACTTGC A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:92163284..92163449 32194978 MeRIP-seq:(Medium) rs576760663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27438349 95023 RMVar_ID_95023 Human_SNP_ID_587919073 m1A Human chr15 - 92734170 92734170 92734170 CGAGAACATGGCCGGAGGCAAAGCTGGAAAGGACAGTGGGAAGGCCAAGGCTAAGGCAGTATCTC CGAGAACATGGCCGGAGGCAAAGCTGGAAAGGGCAGTGGGAAGGCCAAGGCTAAGGCAGTATCTC T C FAM174B,H2AZ2P1 Ensembl:ENSG00000185442,Ensembl:ENSG00000258741 Protein coding,Pseudogene intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:92734120..92734266 26863196 MeRIP-seq:(Medium) rs927153401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1511122,Human_RBP_ID_4341000,Human_RBP_ID_18672015 Human_miRNA_ID_1841160 95024 RMVar_ID_95024 Human_SNP_ID_587919107 m1A Human chr15 + 92734209 92734209 92734209 CAGCTTTGCCTCCGGCCATGTTCTCGGCGCCGACTCCGCCTCCGCCTCCGCCCCGCCGCGCGCCC CAGCTTTGCCTCCGGCCATGTTCTCGGCGCCGGCTCCGCCTCCGCCTCCGCCCCGCCGCGCGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92734159..92734294 26863196 MeRIP-seq:(Medium) rs575710766 Functional Loss SNV dbSNP153 33..33 33 - - - 95025 RMVar_ID_95025 Human_SNP_ID_587919168 m1A Human chr15 + 92734253 92734253 92734253 CCTCCGCCCCGCCGCGCGCCCTCCCGCTGCCGACCCGCGCCGCCGCCGCCGCTCTCCTTCACCTC CCTCCGCCCCGCCGCGCGCCCTCCCGCTGCCGCCCCGCGCCGCCGCCGCCGCTCTCCTTCACCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92734095..92734269 26863196 MeRIP-seq:(Medium) rs1462318954 Functional Loss SNV dbSNP153 33..33 33 - - - 95026 RMVar_ID_95026 Human_SNP_ID_587940910 m1A Human chr15 + 92808217 92808217 92808217 CAGCTTCTCGGGCCCCACCCGCCACCGTCCTCAGAATTTCCCATTTAGAAGGTCCGGGATAGACT CAGCTTCTCGGGCCCCACCCGCCACCGTCCTCGGAATTTCCCATTTAGAAGGTCCGGGATAGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92808187..92808296 26863196 MeRIP-seq:(Medium) rs8040146 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12470,GWAS_ID_12471,GWAS_ID_12472,GWAS_ID_12473,GWAS_ID_12474 95027 RMVar_ID_95027 Human_SNP_ID_587941561 m1A Human chr15 + 92809691 92809691 92809691 TTTCTTTTGTCTCTGCGTTTGCTGCTCCGTGCAAACAAGGAGGACAGAAAACTCTTTATCGTGGC TTTCTTTTGTCTCTGCGTTTGCTGCTCCGTGCGAACAAGGAGGACAGAAAACTCTTTATCGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92809658..92809774 26863196 MeRIP-seq:(Medium) rs1017206311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8426260 95028 RMVar_ID_95028 Human_SNP_ID_587963364 m1A Human chr15 + 92883112 92883099 92883112 GGGCCCCGGCGGCTGGACCCGGCGCGGGCGGGAGGCTCGGGCGGGCGGTCCGGCCCGGGACTCGG GGGCCCCGGCGGCTGGACCC_____________GGCTCGGGCGGGCGGTCCGGCCCGGGACTCGG CGGCGCGGGCGGGA C LINC01578 Ensembl:ENSG00000272888 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:92882851..92883604 26863410 MeRIP-seq:(Medium) rs1157370181 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_467316,Human_RBP_ID_5180325,Human_RBP_ID_5236368,Human_RBP_ID_5418874,Human_RBP_ID_5494953,Human_RBP_ID_8082045,Human_RBP_ID_9324434,Human_RBP_ID_17367025,Human_RBP_ID_17669393,Human_RBP_ID_22370038,Human_RBP_ID_22934609,Human_RBP_ID_23118399,Human_RBP_ID_26778745 Human_Splice_Rec_1646785,Human_Splice_Rec_1646793,Human_Splice_Rec_1646795,Human_Splice_Rec_1646803,Human_Splice_Rec_1646807,Human_Splice_Rec_1646817 Human_miRNA_ID_3162141,Human_miRNA_ID_3211045 95029 RMVar_ID_95029 Human_SNP_ID_587968778 m1A Human chr15 + 92900432 92900431 92900433 TACGCAACTTTCCCTAACTTTCGGGCAGCCTCAGGGGGCCCCCGTAGCCCCCTGCCTTTCCTAGG TACGCAACTTTCCCTAACTTTCGGGCAGCCTC__GGGGCCCCCGTAGCCCCCTGCCTTTCCTAGG CAG C CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92900388..92900459 26863196 MeRIP-seq:(Medium) rs1432921498 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_232317,Human_RBP_ID_759221,Human_RBP_ID_814995,Human_RBP_ID_2461787,Human_RBP_ID_12641740,Human_RBP_ID_17367027,Human_RBP_ID_18672067 Human_miRNA_ID_1973502,Human_miRNA_ID_1973503,Human_miRNA_ID_1975681,Human_miRNA_ID_1975682,Human_miRNA_ID_2295850,Human_miRNA_ID_2295851,Human_miRNA_ID_2613481,Human_miRNA_ID_2613482,Human_miRNA_ID_2715373,Human_miRNA_ID_2715374,Human_miRNA_ID_3051351,Human_miRNA_ID_3051352 RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_98654,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985 95030 RMVar_ID_95030 Human_SNP_ID_587968779 m1A Human chr15 + 92900432 92900432 92900432 TACGCAACTTTCCCTAACTTTCGGGCAGCCTCAGGGGGCCCCCGTAGCCCCCTGCCTTTCCTAGG TACGCAACTTTCCCTAACTTTCGGGCAGCCTCGGGGGGCCCCCGTAGCCCCCTGCCTTTCCTAGG A G CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92900388..92900459 26863196 MeRIP-seq:(Medium) rs751119192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232317,Human_RBP_ID_759221,Human_RBP_ID_814995,Human_RBP_ID_2461787,Human_RBP_ID_12641740,Human_RBP_ID_17367027,Human_RBP_ID_18672067 Human_miRNA_ID_1973502,Human_miRNA_ID_1973503,Human_miRNA_ID_1975681,Human_miRNA_ID_1975682,Human_miRNA_ID_2295850,Human_miRNA_ID_2295851,Human_miRNA_ID_2613481,Human_miRNA_ID_2613482,Human_miRNA_ID_2715373,Human_miRNA_ID_2715374,Human_miRNA_ID_3051351,Human_miRNA_ID_3051352 RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_98654,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985 95031 RMVar_ID_95031 Human_SNP_ID_587979370 m1A Human chr15 - 92937569 92937561 92937569 TTTACTTTTTTTTGTTCTGGCTCACTCTCTGCACTGGTGCCTTGTTCCTGTTCATCTTCTGAGGG TTTACTTTTTTTTGTTCTGGCTCACTCTCTGC________CTTGTTCCTGTTCATCTTCTGAGGG GGCACCAGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92937468..92937625 26863196 MeRIP-seq:(Medium) rs781742188 Functional Loss DEL dbSNP153 33..40 33 - - - 95032 RMVar_ID_95032 Human_SNP_ID_587979897 m1A Human chr15 + 92939536 92939536 92939536 GAAATACTGTTATATAAAGTAGACACCAAATGATAAAGTGAAGACTTAGCCTTTTGTTTCTCTTC GAAATACTGTTATATAAAGTAGACACCAAATGGTAAAGTGAAGACTTAGCCTTTTGTTTCTCTTC A G CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92939532..92939643 26863196 MeRIP-seq:(Medium) rs1488667832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50134,RMVar_hsa_circ_28480,RMVar_hsa_circ_74200,RMVar_hsa_circ_98654,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985,RMVar_hsa_circ_268815,RMVar_hsa_circ_360648,RMVar_hsa_circ_363239,RMVar_hsa_circ_359197,RMVar_hsa_circ_126848,RMVar_hsa_circ_66951,RMVar_hsa_circ_32807,RMVar_hsa_circ_75240,RMVar_hsa_circ_292262,RMVar_hsa_circ_323411,RMVar_hsa_circ_357151,RMVar_hsa_circ_362938,RMVar_hsa_circ_174986,RMVar_hsa_circ_371539,RMVar_hsa_circ_359930,RMVar_hsa_circ_341090,RMVar_hsa_circ_345255,RMVar_hsa_circ_321640,RMVar_hsa_circ_312312,RMVar_hsa_circ_269937,RMVar_hsa_circ_88004,RMVar_hsa_circ_63727,RMVar_hsa_circ_64882,RMVar_hsa_circ_69369,RMVar_hsa_circ_64646,RMVar_hsa_circ_61324,RMVar_hsa_circ_63270,RMVar_hsa_circ_57571,RMVar_hsa_circ_174988,RMVar_hsa_circ_174992,RMVar_hsa_circ_174994,RMVar_hsa_circ_174995,RMVar_hsa_circ_174993,RMVar_hsa_circ_174990,RMVar_hsa_circ_174991,RMVar_hsa_circ_174989,RMVar_hsa_circ_174987,RMVar_hsa_circ_311113,RMVar_hsa_circ_112225,RMVar_hsa_circ_175001,RMVar_hsa_circ_275251,RMVar_hsa_circ_36546,RMVar_hsa_circ_54394,RMVar_hsa_circ_175000,RMVar_hsa_circ_283751,RMVar_hsa_circ_329026,RMVar_hsa_circ_344479,RMVar_hsa_circ_365807,RMVar_hsa_circ_338725,RMVar_hsa_circ_320789,RMVar_hsa_circ_278223,RMVar_hsa_circ_60206,RMVar_hsa_circ_93247,RMVar_hsa_circ_108751,RMVar_hsa_circ_65959,RMVar_hsa_circ_175003,RMVar_hsa_circ_175005,RMVar_hsa_circ_175006,RMVar_hsa_circ_175007,RMVar_hsa_circ_175004,RMVar_hsa_circ_175002 95033 RMVar_ID_95033 Human_SNP_ID_587979898 m1A Human chr15 + 92939536 92939536 92939536 GAAATACTGTTATATAAAGTAGACACCAAATGATAAAGTGAAGACTTAGCCTTTTGTTTCTCTTC GAAATACTGTTATATAAAGTAGACACCAAATGTTAAAGTGAAGACTTAGCCTTTTGTTTCTCTTC A T CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92939532..92939643 26863196 MeRIP-seq:(Medium) rs1488667832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50134,RMVar_hsa_circ_28480,RMVar_hsa_circ_74200,RMVar_hsa_circ_98654,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985,RMVar_hsa_circ_268815,RMVar_hsa_circ_360648,RMVar_hsa_circ_363239,RMVar_hsa_circ_359197,RMVar_hsa_circ_126848,RMVar_hsa_circ_66951,RMVar_hsa_circ_32807,RMVar_hsa_circ_75240,RMVar_hsa_circ_292262,RMVar_hsa_circ_323411,RMVar_hsa_circ_357151,RMVar_hsa_circ_362938,RMVar_hsa_circ_174986,RMVar_hsa_circ_371539,RMVar_hsa_circ_359930,RMVar_hsa_circ_341090,RMVar_hsa_circ_345255,RMVar_hsa_circ_321640,RMVar_hsa_circ_312312,RMVar_hsa_circ_269937,RMVar_hsa_circ_88004,RMVar_hsa_circ_63727,RMVar_hsa_circ_64882,RMVar_hsa_circ_69369,RMVar_hsa_circ_64646,RMVar_hsa_circ_61324,RMVar_hsa_circ_63270,RMVar_hsa_circ_57571,RMVar_hsa_circ_174988,RMVar_hsa_circ_174992,RMVar_hsa_circ_174994,RMVar_hsa_circ_174995,RMVar_hsa_circ_174993,RMVar_hsa_circ_174990,RMVar_hsa_circ_174991,RMVar_hsa_circ_174989,RMVar_hsa_circ_174987,RMVar_hsa_circ_311113,RMVar_hsa_circ_112225,RMVar_hsa_circ_175001,RMVar_hsa_circ_275251,RMVar_hsa_circ_36546,RMVar_hsa_circ_54394,RMVar_hsa_circ_175000,RMVar_hsa_circ_283751,RMVar_hsa_circ_329026,RMVar_hsa_circ_344479,RMVar_hsa_circ_365807,RMVar_hsa_circ_338725,RMVar_hsa_circ_320789,RMVar_hsa_circ_278223,RMVar_hsa_circ_60206,RMVar_hsa_circ_93247,RMVar_hsa_circ_108751,RMVar_hsa_circ_65959,RMVar_hsa_circ_175003,RMVar_hsa_circ_175005,RMVar_hsa_circ_175006,RMVar_hsa_circ_175007,RMVar_hsa_circ_175004,RMVar_hsa_circ_175002 95034 RMVar_ID_95034 Human_SNP_ID_587982429 m1A Human chr15 + 92947691 92947691 92947691 CACGAATGAAGAAGTAGTGTGAGGACAAGGGAAGTAACAGTGGCGTGGAAGGAGTGGATGGGAGA CACGAATGAAGAAGTAGTGTGAGGACAAGGGAGGTAACAGTGGCGTGGAAGGAGTGGATGGGAGA A G CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:92947680..92947764 26863196 MeRIP-seq:(Medium) rs1293483392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10482913,Human_RBP_ID_12643497 RMVar_hsa_circ_50134,RMVar_hsa_circ_28480,RMVar_hsa_circ_74200,RMVar_hsa_circ_98654,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985,RMVar_hsa_circ_360648,RMVar_hsa_circ_363239,RMVar_hsa_circ_359197,RMVar_hsa_circ_126848,RMVar_hsa_circ_66951,RMVar_hsa_circ_32807,RMVar_hsa_circ_75240,RMVar_hsa_circ_292262,RMVar_hsa_circ_323411,RMVar_hsa_circ_362938,RMVar_hsa_circ_174986,RMVar_hsa_circ_371539,RMVar_hsa_circ_359930,RMVar_hsa_circ_345255,RMVar_hsa_circ_312312,RMVar_hsa_circ_269937,RMVar_hsa_circ_88004,RMVar_hsa_circ_63727,RMVar_hsa_circ_64882,RMVar_hsa_circ_64646,RMVar_hsa_circ_63270,RMVar_hsa_circ_57571,RMVar_hsa_circ_174988,RMVar_hsa_circ_174992,RMVar_hsa_circ_174993,RMVar_hsa_circ_174990,RMVar_hsa_circ_174991,RMVar_hsa_circ_174989,RMVar_hsa_circ_174987,RMVar_hsa_circ_112225,RMVar_hsa_circ_175001,RMVar_hsa_circ_275251,RMVar_hsa_circ_36546,RMVar_hsa_circ_175000,RMVar_hsa_circ_283751,RMVar_hsa_circ_329026,RMVar_hsa_circ_344479,RMVar_hsa_circ_365807,RMVar_hsa_circ_320789,RMVar_hsa_circ_60206,RMVar_hsa_circ_108751,RMVar_hsa_circ_65959,RMVar_hsa_circ_175003,RMVar_hsa_circ_175005,RMVar_hsa_circ_175004,RMVar_hsa_circ_175002,RMVar_hsa_circ_56143,RMVar_hsa_circ_269339,RMVar_hsa_circ_74495,RMVar_hsa_circ_62194,RMVar_hsa_circ_83944,RMVar_hsa_circ_117984,RMVar_hsa_circ_95103,RMVar_hsa_circ_100988,RMVar_hsa_circ_175010,RMVar_hsa_circ_175011,RMVar_hsa_circ_175009,RMVar_hsa_circ_62429,RMVar_hsa_circ_16699,RMVar_hsa_circ_60115,RMVar_hsa_circ_67922,RMVar_hsa_circ_175013,RMVar_hsa_circ_318420,RMVar_hsa_circ_368895,RMVar_hsa_circ_73891,RMVar_hsa_circ_61814,RMVar_hsa_circ_62525,RMVar_hsa_circ_61692,RMVar_hsa_circ_175014,RMVar_hsa_circ_59042,RMVar_hsa_circ_175017,RMVar_hsa_circ_286320,RMVar_hsa_circ_351438,RMVar_hsa_circ_378934,RMVar_hsa_circ_175018 95035 RMVar_ID_95035 Human_SNP_ID_587996803 m1A Human chr15 + 93002274 93002274 93002274 GGAGAAACAAATGAGTTCTAGGAAAGACAAAGAAGGGGACAAGGAAAGAAAGAAGTCAAAAGATA GGAGAAACAAATGAGTTCTAGGAAAGACAAAGGAGGGGACAAGGAAAGAAAGAAGTCAAAAGATA A G CHD2 Ensembl:ENSG00000173575 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:93002152..93002368 26863196 MeRIP-seq:(Medium) rs1064795470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887249,Human_RBP_ID_2462184,Human_RBP_ID_3945935,Human_RBP_ID_5523558,Human_RBP_ID_9345324,Human_RBP_ID_24544186,Human_RBP_ID_26327145,Human_RBP_ID_27809960 Human_Splice_Rec_1646932,Human_Splice_Rec_1646933,Human_Splice_Rec_1647112,Human_Splice_Rec_1647113,Human_Splice_Rec_1647368,Human_Splice_Rec_1647394,Human_Splice_Rec_1647395,Human_Splice_Rec_1647414,Human_Splice_Rec_1647415 RMVar_hsa_circ_22375,RMVar_hsa_circ_98654,RMVar_hsa_circ_174984,RMVar_hsa_circ_362938,RMVar_hsa_circ_88004,RMVar_hsa_circ_63270,RMVar_hsa_circ_174987,RMVar_hsa_circ_60206,RMVar_hsa_circ_88492,RMVar_hsa_circ_175022,RMVar_hsa_circ_53788,RMVar_hsa_circ_175023,RMVar_hsa_circ_70647,RMVar_hsa_circ_19468,RMVar_hsa_circ_72524,RMVar_hsa_circ_56036,RMVar_hsa_circ_16759,RMVar_hsa_circ_365470,RMVar_hsa_circ_175038,RMVar_hsa_circ_94734,RMVar_hsa_circ_55449,RMVar_hsa_circ_74275,RMVar_hsa_circ_119721,RMVar_hsa_circ_175041,RMVar_hsa_circ_356133,RMVar_hsa_circ_103601,RMVar_hsa_circ_175048,RMVar_hsa_circ_175043,RMVar_hsa_circ_265214,RMVar_hsa_circ_283661,RMVar_hsa_circ_369031,RMVar_hsa_circ_302819,RMVar_hsa_circ_175045,RMVar_hsa_circ_175046,RMVar_hsa_circ_122989,RMVar_hsa_circ_277927,RMVar_hsa_circ_353321,RMVar_hsa_circ_364817,RMVar_hsa_circ_334097,RMVar_hsa_circ_271889,RMVar_hsa_circ_175050,RMVar_hsa_circ_175051,RMVar_hsa_circ_175049,RMVar_hsa_circ_72838,RMVar_hsa_circ_336105,RMVar_hsa_circ_352757,RMVar_hsa_circ_363894,RMVar_hsa_circ_296564 95036 RMVar_ID_95036 Human_SNP_ID_588000064 m1A Human chr15 + 93014799 93014799 93014799 GGACTCTCTGATATCTCAGTCCCATACCTCACACAACCTTCACCCTCAGAAGCCTCATTTGCCTG GGACTCTCTGATATCTCAGTCCCATACCTCACGCAACCTTCACCCTCAGAAGCCTCATTTGCCTG A G CHD2 Ensembl:ENSG00000173575 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:93014748..93014848 26863196 MeRIP-seq:(Medium) rs1248526429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371944,Human_RBP_ID_17869603,Human_RBP_ID_18529096,Human_RBP_ID_18672225 Human_miRNA_ID_2007391 RMVar_hsa_circ_63270,RMVar_hsa_circ_60206,RMVar_hsa_circ_88492,RMVar_hsa_circ_175022,RMVar_hsa_circ_72524,RMVar_hsa_circ_103601,RMVar_hsa_circ_175043,RMVar_hsa_circ_265214,RMVar_hsa_circ_302819,RMVar_hsa_circ_175045,RMVar_hsa_circ_364817,RMVar_hsa_circ_271889,RMVar_hsa_circ_175051,RMVar_hsa_circ_175053,RMVar_hsa_circ_336105,RMVar_hsa_circ_363894,RMVar_hsa_circ_283415,RMVar_hsa_circ_309356,RMVar_hsa_circ_281865,RMVar_hsa_circ_175054,RMVar_hsa_circ_175055,RMVar_hsa_circ_349198,RMVar_hsa_circ_378870,RMVar_hsa_circ_90289,RMVar_hsa_circ_277419,RMVar_hsa_circ_175059,RMVar_hsa_circ_175060 95037 RMVar_ID_95037 Human_SNP_ID_588002910 m1A Human chr15 - 93025110 93025110 93025110 CACACACTGTTCACCAGGTCCCAGCAGCCTCCATGCACCAGTTCCTGCCCCGACCATGCACTAAG CACACACTGTTCACCAGGTCCCAGCAGCCTCCGTGCACCAGTTCCTGCCCCGACCATGCACTAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:93025060..93025281 26863196 MeRIP-seq:(Medium) rs1031950690 Functional Loss SNV dbSNP153 33..33 33 - - - 95038 RMVar_ID_95038 Human_SNP_ID_588002919 m1A Human chr15 - 93025155 93025155 93025155 CATCAGCAGCATCCATCATGTCAGAGTGAACCAAATCAACCAAATCACACACTGTTCACCAGGTC CATCAGCAGCATCCATCATGTCAGAGTGAACCCAATCAACCAAATCACACACTGTTCACCAGGTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:93025105..93025241 26863196 MeRIP-seq:(Medium) rs1335554471 Functional Loss SNV dbSNP153 33..33 33 - - - 95039 RMVar_ID_95039 Human_SNP_ID_588009434 m1A Human chr15 + 93044609 93044609 93044609 CGTGCGTGTGGCGGGCACAGGGGGCCCCACGGATCGGCGAGCAGCAGTCGGCCGGGCCTTTCAGT CGTGCGTGTGGCGGGCACAGGGGGCCCCACGGGTCGGCGAGCAGCAGTCGGCCGGGCCTTTCAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:93044558..93044659 26863196 MeRIP-seq:(Medium) rs557054421 Functional Loss SNV dbSNP153 33..33 33 - - - 95040 RMVar_ID_95040 Human_SNP_ID_588009465 m1A Human chr15 + 93044671 93044671 93044671 AGTGCATTGCGAGGGGGAAGGAGCTGACTCTGACGGTTCCCAGTGTGTCTCTGGTGGGGGTGGGG AGTGCATTGCGAGGGGGAAGGAGCTGACTCTGTCGGTTCCCAGTGTGTCTCTGGTGGGGGTGGGG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:93044567..93044711 26863196 MeRIP-seq:(Medium) rs1341360146 Functional Loss SNV dbSNP153 33..33 33 - - - 95041 RMVar_ID_95041 Human_SNP_ID_588878460 m1A Human chr15 - 96330819 96330819 96330819 GAGGAGGAGAAGAAGAAAACACACACGCGCGCACGCACACACACACCGCGGAGAGAAAAGAACAG GAGGAGGAGAAGAAGAAAACACACACGCGCGCGCGCACACACACACCGCGGAGAGAAAAGAACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:96326334..96331296 26863196 MeRIP-seq:(Medium) rs1330006841 Functional Loss SNV dbSNP153 33..33 33 - - - 95042 RMVar_ID_95042 Human_SNP_ID_588878584 m1A Human chr15 + 96331097 96331070 96331097 GCAGCGGCTCCGGCGGCGGCAGCAGCGGCAGCAGCGACTTCAGCGGCGGCGGCGGCGCTAGACGC GCAGCG___________________________GCGACTTCAGCGGCGGCGGCGGCGCTAGACGC GGCTCCGGCGGCGGCAGCAGCGGCAGCA G NR2F2 Ensembl:ENSG00000185551 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:96331046..96331147 32194978 MeRIP-seq:(Medium) rs1258985082 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_232823,Human_RBP_ID_22439939 95043 RMVar_ID_95043 Human_SNP_ID_588878620 m1A Human chr15 - 96331156 96331148 96331157 CGGGCCGCCGCTGCCGCCGGAGCCGCCGCCGAAGCCGCCGGGTCGGGCCCGGAGCCGCTGCGTCT CGGGCCGCCGCTGCCGCCGGAGCCGCCGCCG_________GGTCGGGCCCGGAGCCGCTGCGTCT CCGGCGGCTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:96331096..96331196 26863410 MeRIP-seq:(Medium) rs1430587353 Functional Loss DEL dbSNP153 32..40 33 - - - 95044 RMVar_ID_95044 Human_SNP_ID_588878912 m1A Human chr15 - 96331932 96331928 96331932 GTGGCTCGGGGGCTGGTTGGTTGAGGTTGGTTAGTTTTTCCTTTTTTGTTTTTGCTTTTGCAAAG GTGGCTCGGGGGCTGGTTGGTTGAGGTTGGTT____TTTCCTTTTTTGTTTTTGCTTTTGCAAAG AAACT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:96331791..96332190 26863196 MeRIP-seq:(Medium) rs1315014169 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6482429 95045 RMVar_ID_95045 Human_SNP_ID_588878914 m1A Human chr15 - 96331932 96331932 96331932 GTGGCTCGGGGGCTGGTTGGTTGAGGTTGGTTAGTTTTTCCTTTTTTGTTTTTGCTTTTGCAAAG GTGGCTCGGGGGCTGGTTGGTTGAGGTTGGTTTGTTTTTCCTTTTTTGTTTTTGCTTTTGCAAAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:96331791..96332190 26863196 MeRIP-seq:(Medium) rs901353840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6482429 95046 RMVar_ID_95046 Human_SNP_ID_588879033 m1A Human chr15 + 96332240 96332240 96332240 GGCGCCCCGCACACGCCACAGACGCCCGGCCAAGGGGGCCCAGCCAGCACGCCAGCCCAGACGGC GGCGCCCCGCACACGCCACAGACGCCCGGCCAGGGGGGCCCAGCCAGCACGCCAGCCCAGACGGC A G NR2F2 Ensembl:ENSG00000185551 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:96332139..96332587 26863410 MeRIP-seq:(Medium) rs1375546674 Functional Loss SNV dbSNP153 33..33 33 - - - 95047 RMVar_ID_95047 Human_SNP_ID_589297642 m1A Human chr15 - 97965625 97965625 97965625 AGTTGAAAGCGAAATGGAAATTCATGTTTTCCAGGCTGTAATAAAATGATGCCTTCACCTATAAG AGTTGAAAGCGAAATGGAAATTCATGTTTTCCTGGCTGTAATAAAATGATGCCTTCACCTATAAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:97960846..97965625 32194978 MeRIP-seq:(Medium) rs770898973 Functional Loss SNV dbSNP153 33..33 33 - - - 95048 RMVar_ID_95048 Human_SNP_ID_589484720 m1A Human chr15 + 98648649 98648649 98648649 AAAAGGGAAAAAACCCGAGGAGGAGCGAGCGCACCAGGCGAACTCGAGAGAGGCGGGAGAGCGAG AAAAGGGAAAAAACCCGAGGAGGAGCGAGCGCGCCAGGCGAACTCGAGAGAGGCGGGAGAGCGAG A G IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:98648557..98649431 26863196 MeRIP-seq:(Medium) rs930955483 Functional Loss SNV dbSNP153 33..33 33 - - - 95049 RMVar_ID_95049 Human_SNP_ID_589484732 m1A Human chr15 + 98648674 98648674 98648674 CGAGCGCACCAGGCGAACTCGAGAGAGGCGGGAGAGCGAGAGGGACGCCGCCAGCGAGCCTGCCC CGAGCGCACCAGGCGAACTCGAGAGAGGCGGGGGAGCGAGAGGGACGCCGCCAGCGAGCCTGCCC A G IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:98648575..98648804 26863196 MeRIP-seq:(Medium) rs1456012133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4341647 95050 RMVar_ID_95050 Human_SNP_ID_589484865 m1A Human chr15 + 98648920 98648920 98648920 GGCGGCGGCGCAGAGCCGGGCGGCGCGGCGGGAGTGCTGAGCGCGGCGCGGCCGGCCCGCCGCTT GGCGGCGGCGCAGAGCCGGGCGGCGCGGCGGGCGTGCTGAGCGCGGCGCGGCCGGCCCGCCGCTT A C IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:98648881..98649012 26863196 MeRIP-seq:(Medium) rs868696482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4341659 95051 RMVar_ID_95051 Human_SNP_ID_589484895 m1A Human chr15 + 98649011 98648987 98649011 GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA GCTCGCCGC________________________GGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA CGGCGGCGGCGGCGCTGAGGGAGGA C IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98648876..98649242 26863196 MeRIP-seq:(Medium) rs1053681925 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_4342486,Human_RBP_ID_5523575,Human_RBP_ID_22440202 95052 RMVar_ID_95052 Human_SNP_ID_589484902 m1A Human chr15 + 98649011 98648993 98649011 GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA GCTCGCCGCGGCGGC__________________GGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA CGGCGGCGCTGAGGGAGGA C IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98648876..98649242 26863196 MeRIP-seq:(Medium) rs891986395 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_4342486,Human_RBP_ID_5523575,Human_RBP_ID_22440202 95053 RMVar_ID_95053 Human_SNP_ID_589484906 m1A Human chr15 - 98649002 98649002 98649002 TCCTGGCTCCGCTCGCCGCCGCCTCCTCCCTCAGCGCCGCCGCCGCCGCGGCGAGCTCCTTCCCA TCCTGGCTCCGCTCGCCGCCGCCTCCTCCCTCGGCGCCGCCGCCGCCGCGGCGAGCTCCTTCCCA T C IRAIN,IRAIN:2,IRAIN:3,IRAIN:4 RNACentral:URS0000E972DF,RNACentral:URS00007E3F3D,RNACentral:URS0000D5B6C0,RNACentral:URS00009C4D20 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:98648856..98649025 26863196 MeRIP-seq:(Medium) rs1287962731 Functional Loss SNV dbSNP153 33..33 33 - - - 95054 RMVar_ID_95054 Human_SNP_ID_589484907 m1A Human chr15 + 98649004 98649004 98649004 GGAAGGAGCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGG GGAAGGAGCTCGCCGCGGCGGCGGCGGCGCTGTGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGG A T IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:98648913..98649047 26863196 MeRIP-seq:(Medium) rs1236421280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232647,Human_RBP_ID_4341663,Human_RBP_ID_5523575,Human_RBP_ID_22440202 95055 RMVar_ID_95055 Human_SNP_ID_589484909 m1A Human chr15 + 98649011 98649011 98649011 GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGCGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA A C IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98648876..98649242 26863196 MeRIP-seq:(Medium) rs1334201966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342486,Human_RBP_ID_5523575,Human_RBP_ID_22440202 95056 RMVar_ID_95056 Human_SNP_ID_589484910 m1A Human chr15 + 98649011 98649011 98649011 GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGAGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA GCTCGCCGCGGCGGCGGCGGCGCTGAGGGAGGGGGCGGCGGCGAGCGGAGCCAGGAGGAGGAGGA A G IGF1R Ensembl:ENSG00000140443 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98648876..98649242 26863196 MeRIP-seq:(Medium) rs1334201966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342486,Human_RBP_ID_5523575,Human_RBP_ID_22440202 95057 RMVar_ID_95057 Human_SNP_ID_589485078 m1A Human chr15 - 98649347 98649347 98649347 GGGCGGCCCCTCAGCGCCGGCAGCAGCGGCCCAGGGCTCGGCGGAGTCGGGAACCCGAGGCGCGC GGGCGGCCCCTCAGCGCCGGCAGCAGCGGCCCGGGGCTCGGCGGAGTCGGGAACCCGAGGCGCGC T C IRAIN,IRAIN:2,IRAIN:3,IRAIN:4 RNACentral:URS0000E972DF,RNACentral:URS00007E3F3D,RNACentral:URS0000D5B6C0,RNACentral:URS00009C4D20 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98649297..98649426 26863196 MeRIP-seq:(Medium) rs1216321225 Functional Loss SNV dbSNP153 33..33 33 - - - 95058 RMVar_ID_95058 Human_SNP_ID_589489598 m1A Human chr15 + 98663268 98663268 98663268 GTCCCAGTTGATGGAGAGGCAGGACCCGCAAAACAGGTTGGCTGCAGGACTGGGGGCGGTAGCAC GTCCCAGTTGATGGAGAGGCAGGACCCGCAAAGCAGGTTGGCTGCAGGACTGGGGGCGGTAGCAC A G IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98663218..98663314 26863196 MeRIP-seq:(Medium) rs1160918323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17188205 95059 RMVar_ID_95059 Human_SNP_ID_589501300 m1A Human chr15 - 98704736 98704736 98704736 ACACTTCCCTCCCAAGGTACACCACCCTCTGCAGGACACCGCTCTGGCCCTTCTTTTCATGGTCT ACACTTCCCTCCCAAGGTACACCACCCTCTGCGGGACACCGCTCTGGCCCTTCTTTTCATGGTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98704733..98704851 26863196 MeRIP-seq:(Medium) rs944753193 Functional Loss SNV dbSNP153 33..33 33 - - - 95060 RMVar_ID_95060 Human_SNP_ID_589511755 m1A Human chr15 + 98744513 98744513 98744513 AGAGAAGCATGGCTGTGCACAGGGGAGGTGGGATGGCAGCCAGGGAGGAGCAGAGGTGGAATGTG AGAGAAGCATGGCTGTGCACAGGGGAGGTGGGCTGGCAGCCAGGGAGGAGCAGAGGTGGAATGTG A C IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:98744382..98744692;chr15:98744368..98744713 26863196 MeRIP-seq:(Medium) rs1263970501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41914,Human_RBP_ID_6483035,Human_RBP_ID_8182718,Human_RBP_ID_9418516,Human_RBP_ID_12648409,Human_RBP_ID_23273505,Human_RBP_ID_26779048 RMVar_hsa_circ_175102,RMVar_hsa_circ_318859,RMVar_hsa_circ_372350,RMVar_hsa_circ_373599,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_284004,RMVar_hsa_circ_125337,RMVar_hsa_circ_175104,RMVar_hsa_circ_175105,RMVar_hsa_circ_175103,RMVar_hsa_circ_175100,RMVar_hsa_circ_175101,RMVar_hsa_circ_175099 95061 RMVar_ID_95061 Human_SNP_ID_589511756 m1A Human chr15 + 98744513 98744513 98744513 AGAGAAGCATGGCTGTGCACAGGGGAGGTGGGATGGCAGCCAGGGAGGAGCAGAGGTGGAATGTG AGAGAAGCATGGCTGTGCACAGGGGAGGTGGGGTGGCAGCCAGGGAGGAGCAGAGGTGGAATGTG A G IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:98744382..98744692;chr15:98744368..98744713 26863196 MeRIP-seq:(Medium) rs1263970501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41914,Human_RBP_ID_6483035,Human_RBP_ID_8182718,Human_RBP_ID_9418516,Human_RBP_ID_12648409,Human_RBP_ID_23273505,Human_RBP_ID_26779048 RMVar_hsa_circ_175102,RMVar_hsa_circ_318859,RMVar_hsa_circ_372350,RMVar_hsa_circ_373599,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_284004,RMVar_hsa_circ_125337,RMVar_hsa_circ_175104,RMVar_hsa_circ_175105,RMVar_hsa_circ_175103,RMVar_hsa_circ_175100,RMVar_hsa_circ_175101,RMVar_hsa_circ_175099 95062 RMVar_ID_95062 Human_SNP_ID_589512581 m1A Human chr15 + 98747644 98747644 98747644 GCATGAGAACTGTGTCGGGTGGTCCTGAAGAGATTAGTGGATTAGAAGGAGATTTGGAGATTTTT GCATGAGAACTGTGTCGGGTGGTCCTGAAGAGTTTAGTGGATTAGAAGGAGATTTGGAGATTTTT A T IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:98747640..98747770 26863196 MeRIP-seq:(Medium) rs1317034928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12648468 RMVar_hsa_circ_175102,RMVar_hsa_circ_318859,RMVar_hsa_circ_372350,RMVar_hsa_circ_373599,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_284004,RMVar_hsa_circ_125337,RMVar_hsa_circ_175104,RMVar_hsa_circ_175105,RMVar_hsa_circ_175103,RMVar_hsa_circ_175100,RMVar_hsa_circ_175101,RMVar_hsa_circ_175099 95063 RMVar_ID_95063 Human_SNP_ID_589517845 m1A Human chr15 - 98765964 98765964 98765964 ACCTTGGTAAGGGGTTGCACCACTGCCACTGCACAGAACCAGACACCCTCTCCCTTGCGTGGCAT ACCTTGGTAAGGGGTTGCACCACTGCCACTGCGCAGAACCAGACACCCTCTCCCTTGCGTGGCAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:98765959..98766085 26863196 MeRIP-seq:(Medium) rs1164954611 Functional Loss SNV dbSNP153 33..33 33 - - - 95064 RMVar_ID_95064 Human_SNP_ID_589532208 m1A Human chr15 + 98818369 98818369 98818369 CAATACACAGTGGAAGTTGGGGATGAGTGAGAAGCACAAGAGTGGCACACTGATTTCTACAACAG CAATACACAGTGGAAGTTGGGGATGAGTGAGAGGCACAAGAGTGGCACACTGATTTCTACAACAG A G IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:98818365..98818478 26863196 MeRIP-seq:(Medium) rs1170062385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175102,RMVar_hsa_circ_318859,RMVar_hsa_circ_372350,RMVar_hsa_circ_373599,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_284004,RMVar_hsa_circ_125337,RMVar_hsa_circ_175104,RMVar_hsa_circ_175105,RMVar_hsa_circ_175103,RMVar_hsa_circ_175100,RMVar_hsa_circ_175101,RMVar_hsa_circ_175099 95065 RMVar_ID_95065 Human_SNP_ID_589560293 m1A Human chr15 + 98916727 98916727 98916727 GCCGACGGCACCATCGACATTGAGGAGGTCACAGAGAACCCCAAGACTGAGGTGTGTGGTGGGGA GCCGACGGCACCATCGACATTGAGGAGGTCACCGAGAACCCCAAGACTGAGGTGTGTGGTGGGGA A C IGF1R Ensembl:ENSG00000140443 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:98916676..98916918 26863196 MeRIP-seq:(Medium) rs1365057142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42007,Human_RBP_ID_5523580,Human_RBP_ID_12650602,Human_RBP_ID_17689437 Human_Splice_Rec_1649430,Human_Splice_Rec_1649470,Human_Splice_Rec_1649510,Human_Splice_Rec_1649558 Human_miRNA_ID_943574,Human_miRNA_ID_1051546 RMVar_hsa_circ_12520,RMVar_hsa_circ_372350,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_175100,RMVar_hsa_circ_175101,RMVar_hsa_circ_175099,RMVar_hsa_circ_336504,RMVar_hsa_circ_374260,RMVar_hsa_circ_38472,RMVar_hsa_circ_175114,RMVar_hsa_circ_175115,RMVar_hsa_circ_24360,RMVar_hsa_circ_32268,RMVar_hsa_circ_330334,RMVar_hsa_circ_332342,RMVar_hsa_circ_175118,RMVar_hsa_circ_370628,RMVar_hsa_circ_27157,RMVar_hsa_circ_13020,RMVar_hsa_circ_175120,RMVar_hsa_circ_175121,RMVar_hsa_circ_266373,RMVar_hsa_circ_175122,RMVar_hsa_circ_175123,RMVar_hsa_circ_175125,RMVar_hsa_circ_42036,RMVar_hsa_circ_296903,RMVar_hsa_circ_362204,RMVar_hsa_circ_175124,RMVar_hsa_circ_309360 95066 RMVar_ID_95066 Human_SNP_ID_589567779 m1A Human chr15 - 98942883 98942883 98942883 GGAAGAGAGGGCGCAGAGTCACACGCTGGAGCAGGCACCACTGCTGTCACAGCAGAGGACCCTAC GGAAGAGAGGGCGCAGAGTCACACGCTGGAGCGGGCACCACTGCTGTCACAGCAGAGGACCCTAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:98942878..98942991 26863196 MeRIP-seq:(Medium) rs1458171249 Functional Loss SNV dbSNP153 33..33 33 - - - 95067 RMVar_ID_95067 Human_SNP_ID_589573622 m1A Human chr15 - 98960823 98960823 98960823 TTTGGTACATCTCTGTCTACCCCTAGGGAAGGAGGTGAGGGAGAAGTTGAGAGGGCAGCCTGGAG TTTGGTACATCTCTGTCTACCCCTAGGGAAGGTGGTGAGGGAGAAGTTGAGAGGGCAGCCTGGAG T A AC036108.1 Ensembl:ENSG00000259475 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:98960773..98960979 26863196 MeRIP-seq:(Medium) rs998974068 Functional Loss SNV dbSNP153 33..33 33 - - - 95068 RMVar_ID_95068 Human_SNP_ID_589615308 m1A Human chr15 + 99105132 99105110 99105132 AGCGGCGAGGCCGGAGCGTCGCGGCGGAGAGGACGAGACCGGGACAAGACCAGGGCAGGAGGGAG AGCGGCGAGGC______________________CGAGACCGGGACAAGACCAGGGCAGGAGGGAG CCGGAGCGTCGCGGCGGAGAGGA C SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:99105082..99105536 26863196 MeRIP-seq:(Medium) rs1202391297 Functional Loss DEL dbSNP153 12..33 33 - - - 95069 RMVar_ID_95069 Human_SNP_ID_589615799 m1A Human chr15 - 99105887 99105887 99105887 CTCGCGCCGCAGCGCCTCTGCCTCCTGCGCGCACAGCCGCGTCTCTTCCTCCGCCTGGAGTCTGC CTCGCGCCGCAGCGCCTCTGCCTCCTGCGCGCGCAGCCGCGTCTCTTCCTCCGCCTGGAGTCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:99105717..99105964 26863196 MeRIP-seq:(Medium) rs1555482649 Functional Loss SNV dbSNP153 33..33 33 - - - 95070 RMVar_ID_95070 Human_SNP_ID_589615885 m1A Human chr15 + 99105971 99105950 99105971 TGCGCGCGCGGCTGGAGGACGCGCTGCTGCGGATGCGCGAGGAGTACGGGATACAGGCCGAGGAG TGCGCGCGCGGC_____________________TGCGCGAGGAGTACGGGATACAGGCCGAGGAG CTGGAGGACGCGCTGCTGCGGA C SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:99105926..99106025 26863196 MeRIP-seq:(Medium) rs781900681 Functional Loss DEL dbSNP153 13..33 33 - - - Human_Splice_Rec_1649669,Human_Splice_Rec_1649675,Human_Splice_Rec_1649683 RMVar_hsa_circ_118267,RMVar_hsa_circ_175137 95071 RMVar_ID_95071 Human_SNP_ID_589615898 m1A Human chr15 + 99105971 99105971 99105971 TGCGCGCGCGGCTGGAGGACGCGCTGCTGCGGATGCGCGAGGAGTACGGGATACAGGCCGAGGAG TGCGCGCGCGGCTGGAGGACGCGCTGCTGCGGCTGCGCGAGGAGTACGGGATACAGGCCGAGGAG A C SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:99105926..99106025 26863196 MeRIP-seq:(Medium) rs932744574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1649669,Human_Splice_Rec_1649675,Human_Splice_Rec_1649683 RMVar_hsa_circ_118267,RMVar_hsa_circ_175137 95072 RMVar_ID_95072 Human_SNP_ID_589615899 m1A Human chr15 + 99105971 99105971 99105971 TGCGCGCGCGGCTGGAGGACGCGCTGCTGCGGATGCGCGAGGAGTACGGGATACAGGCCGAGGAG TGCGCGCGCGGCTGGAGGACGCGCTGCTGCGGGTGCGCGAGGAGTACGGGATACAGGCCGAGGAG A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:99105926..99106025 26863196 MeRIP-seq:(Medium) rs932744574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1649669,Human_Splice_Rec_1649675,Human_Splice_Rec_1649683 RMVar_hsa_circ_118267,RMVar_hsa_circ_175137 95073 RMVar_ID_95073 Human_SNP_ID_589615910 m1A Human chr15 + 99105989 99105989 99105989 ACGCGCTGCTGCGGATGCGCGAGGAGTACGGGATACAGGCCGAGGAGCGGCAGGTCCGTGCGCGG ACGCGCTGCTGCGGATGCGCGAGGAGTACGGGCTACAGGCCGAGGAGCGGCAGGTCCGTGCGCGG A C SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:99105715..99106025 26863196 MeRIP-seq:(Medium) rs1201744453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1649669,Human_Splice_Rec_1649675,Human_Splice_Rec_1649683 RMVar_hsa_circ_118267,RMVar_hsa_circ_175137 95074 RMVar_ID_95074 Human_SNP_ID_589615911 m1A Human chr15 + 99105989 99105989 99105989 ACGCGCTGCTGCGGATGCGCGAGGAGTACGGGATACAGGCCGAGGAGCGGCAGGTCCGTGCGCGG ACGCGCTGCTGCGGATGCGCGAGGAGTACGGGGTACAGGCCGAGGAGCGGCAGGTCCGTGCGCGG A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:99105715..99106025 26863196 MeRIP-seq:(Medium) rs1201744453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1649669,Human_Splice_Rec_1649675,Human_Splice_Rec_1649683 RMVar_hsa_circ_118267,RMVar_hsa_circ_175137 95075 RMVar_ID_95075 Human_SNP_ID_589619940 m1A Human chr15 + 99120345 99120345 99120345 GAGGCACGCAGGGAGGGCTTCCTGAAGAGGCAATGCTTGATTCTTGTAGGAAGAGAAGCTGGAAA GAGGCACGCAGGGAGGGCTTCCTGAAGAGGCAGTGCTTGATTCTTGTAGGAAGAGAAGCTGGAAA A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:99120344..99120412 26863196 MeRIP-seq:(Medium) rs1213309992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81728,RMVar_hsa_circ_175138 95076 RMVar_ID_95076 Human_SNP_ID_589620059 m1A Human chr15 + 99120758 99120758 99120758 GGTGATGGGGAGGGAGTTGTGAGAATCAGGGGAGGCTTCTAGAGGGATTGAAGATTGATGAAGGT GGTGATGGGGAGGGAGTTGTGAGAATCAGGGGGGGCTTCTAGAGGGATTGAAGATTGATGAAGGT A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:99120755..99120852 26863196 MeRIP-seq:(Medium) rs924991483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81728,RMVar_hsa_circ_175138 95077 RMVar_ID_95077 Human_SNP_ID_589622467 m1A Human chr15 + 99129997 99129997 99129997 AAACCTAAGATGGGAAGAATTGACAAAGTTAGATAAGGAAGCGAGACAGAGAGAAAGCCAGCAGA AAACCTAAGATGGGAAGAATTGACAAAGTTAGGTAAGGAAGCGAGACAGAGAGAAAGCCAGCAGA A G SYNM Ensembl:ENSG00000182253 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:99129946..99130079 26863196 MeRIP-seq:(Medium) rs782577182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43460 95078 RMVar_ID_95078 Human_SNP_ID_589622923 m1A Human chr15 - 99131020 99131020 99131020 GAGAGGGCGCTGGGACATCCAAGGGCTTCACAACCTTCTCGCCCACTGCACCGTCCTTCTGTGTC GAGAGGGCGCTGGGACATCCAAGGGCTTCACAGCCTTCTCGCCCACTGCACCGTCCTTCTGTGTC T C AC036108.2 Ensembl:ENSG00000261054 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:99130970..99131072 32194978 MeRIP-seq:(Medium) rs782341979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5288211,Human_RBP_ID_17869997 95079 RMVar_ID_95079 Human_SNP_ID_589646438 m1A Human chr15 - 99226683 99226683 99226683 TTCCAGGGAGAGGAAACAGCACACATAAATCTACAGGGTAGGCACAAGCAGGACATATCTGAAGC TTCCAGGGAGAGGAAACAGCACACATAAATCTGCAGGGTAGGCACAAGCAGGACATATCTGAAGC T C TTC23 Ensembl:ENSG00000103852 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:99226663..99226767 26863196 MeRIP-seq:(Medium) rs1223628677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124920,RMVar_hsa_circ_266999,RMVar_hsa_circ_175140,RMVar_hsa_circ_74686,RMVar_hsa_circ_318991,RMVar_hsa_circ_353175,RMVar_hsa_circ_352876,RMVar_hsa_circ_297725,RMVar_hsa_circ_175141 95080 RMVar_ID_95080 Human_SNP_ID_589733225 m1A Human chr15 + 99566284 99566284 99566284 GGGACCCCTGGACGAGGCCGTGTCCGGCTTGGAGGGGGCCAGGGTCGCGTTCGCGCATTGGCGGG GGGACCCCTGGACGAGGCCGTGTCCGGCTTGGGGGGGGCCAGGGTCGCGTTCGCGCATTGGCGGG A G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:99566280..99566369 26863196 MeRIP-seq:(Medium) rs1481481447 Functional Loss SNV dbSNP153 33..33 33 - - - 95081 RMVar_ID_95081 Human_SNP_ID_589770008 m1A Human chr15 - 99708852 99708852 99708852 CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACAGGCACACCCTCTCCCAAGAGCACTCTGCCTCC CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACTGGCACACCCTCTCCCAAGAGCACTCTGCCTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:99708828..99708934 26863196 MeRIP-seq:(Medium) rs167805 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12475,GWAS_ID_12476,GWAS_ID_12477 95082 RMVar_ID_95082 Human_SNP_ID_589770009 m1A Human chr15 - 99708852 99708852 99708852 CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACAGGCACACCCTCTCCCAAGAGCACTCTGCCTCC CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACGGGCACACCCTCTCCCAAGAGCACTCTGCCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:99708828..99708934 26863196 MeRIP-seq:(Medium) rs167805 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12475,GWAS_ID_12476,GWAS_ID_12477 95083 RMVar_ID_95083 Human_SNP_ID_590027247 m1A Human chr15 - 100600831 100600831 100600831 TTCAGAAGGAAGTGGGTGTAGGGTGGGCCTGGATACAACCACTTTGGAAGGGATCGGTTGCAGTT TTCAGAAGGAAGTGGGTGTAGGGTGGGCCTGGTTACAACCACTTTGGAAGGGATCGGTTGCAGTT T A LINS1 Ensembl:ENSG00000140471 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:100600781..100600985 26863196 MeRIP-seq:(Medium) rs141285520 Functional Loss SNV dbSNP153 33..33 33 - - - 95084 RMVar_ID_95084 Human_SNP_ID_590027248 m1A Human chr15 - 100600831 100600831 100600831 TTCAGAAGGAAGTGGGTGTAGGGTGGGCCTGGATACAACCACTTTGGAAGGGATCGGTTGCAGTT TTCAGAAGGAAGTGGGTGTAGGGTGGGCCTGGGTACAACCACTTTGGAAGGGATCGGTTGCAGTT T C LINS1 Ensembl:ENSG00000140471 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:100600781..100600985 26863196 MeRIP-seq:(Medium) rs141285520 Functional Loss SNV dbSNP153 33..33 33 - - - 95085 RMVar_ID_95085 Human_SNP_ID_590076645 m1A Human chr15 + 100786418 100786367 100786418 GTGTGTGAGTGTGCGTGTGTATGTGTGTGTGAATGTGTGTGTGAGAGTGTGTGTGCGTGTCAATG _________________________________TGTGTGTGTGAGAGTGTGTGTGCGTGTCAATG GTGTGTGAGTGTGTGTCGTGTGTGTGAGTGTGCGTGTGTATGTGTGTGTGAA G AC087762.1 Ensembl:ENSG00000259579 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:100786147..100786453 26863196 MeRIP-seq:(Medium) rs1567147013 Functional Loss DEL dbSNP153 1..33 33 - - - 95086 RMVar_ID_95086 Human_SNP_ID_590076662 m1A Human chr15 - 100786385 100786381 100786385 TCACACACACATACACACGCACACTCACACACACGACACACACTCACACACATTCACACACATAA TCACACACACATACACACGCACACTCACACAC____CACACACTCACACACATTCACACACATAA GTCGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:100786166..100786441 26863196 MeRIP-seq:(Medium) rs778423023 Functional Loss DEL dbSNP153 33..36 33 - - - 95087 RMVar_ID_95087 Human_SNP_ID_590076676 m1A Human chr15 - 100786385 100786385 100786385 TCACACACACATACACACGCACACTCACACACACGACACACACTCACACACATTCACACACATAA TCACACACACATACACACGCACACTCACACACGCGACACACACTCACACACATTCACACACATAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:100786166..100786441 26863196 MeRIP-seq:(Medium) rs76834446 Functional Loss SNV dbSNP153 33..33 33 - - - 95088 RMVar_ID_95088 Human_SNP_ID_590076717 m1A Human chr15 + 100786418 100786418 100786418 GTGTGTGAGTGTGCGTGTGTATGTGTGTGTGAATGTGTGTGTGAGAGTGTGTGTGCGTGTCAATG GTGTGTGAGTGTGCGTGTGTATGTGTGTGTGAGTGTGTGTGTGAGAGTGTGTGTGCGTGTCAATG A G AC087762.1 Ensembl:ENSG00000259579 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:100786147..100786453 26863196 MeRIP-seq:(Medium) rs375185890 Functional Loss SNV dbSNP153 33..33 33 - - - 95089 RMVar_ID_95089 Human_SNP_ID_590093103 m1A Human chr15 - 100849860 100849860 100849860 GTTTCCTCGTCTGGGGAGCGCAGCAGTCTCATAGCTGCCGTGAGAGGGTTCGCGACAGAATCACC GTTTCCTCGTCTGGGGAGCGCAGCAGTCTCATTGCTGCCGTGAGAGGGTTCGCGACAGAATCACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:100849809..100849915 26863196 MeRIP-seq:(Medium) rs555995683 Functional Loss SNV dbSNP153 33..33 33 - - - 95090 RMVar_ID_95090 Human_SNP_ID_590096552 m1A Human chr15 + 100863002 100863001 100863002 GTCTCGAAAATAAACAAATAAAGAAAGGTTCCAAGGATGGTCTGGAGGACAAACAAAGGAGGAGA GTCTCGAAAATAAACAAATAAAGAAAGGTTCC_AGGATGGTCTGGAGGACAAACAAAGGAGGAGA CA C AC015712.6,AC015712.5,AC015712.4 Ensembl:ENSG00000272808,Ensembl:ENSG00000272639,Ensembl:ENSG00000259604 lincRNA,lincRNA,lincRNA exon,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:100862951..100863104 26863196 MeRIP-seq:(Medium) rs1371171926 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5569642 Human_miRNA_ID_3164681,Human_miRNA_ID_3178686,Human_miRNA_ID_3194146 95091 RMVar_ID_95091 Human_SNP_ID_590096756 m1A Human chr15 - 100863880 100863880 100863880 TTTGACTCTGTAACACGGTGACCACAAGCCCCATTCCACTGGCCGACACGGTCCCAAATATTTCC TTTGACTCTGTAACACGGTGACCACAAGCCCCTTTCCACTGGCCGACACGGTCCCAAATATTTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:100863830..100864097 26863196 MeRIP-seq:(Medium) rs1426123602 Functional Loss SNV dbSNP153 33..33 33 - - - 95092 RMVar_ID_95092 Human_SNP_ID_590100736 m1A Human chr15 - 100879862 100879862 100879862 TCCCTGGCCCGAGGCGCCCTAGTCTGCGGCGCACCGGCTCGGCCCGGACACTGCGCAGCCCGCTC TCCCTGGCCCGAGGCGCCCTAGTCTGCGGCGCGCCGGCTCGGCCCGGACACTGCGCAGCCCGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:100879770..100880000;chr15:100879801..100880025 26863196 MeRIP-seq:(Medium) rs993313886 Functional Loss SNV dbSNP153 33..33 33 - - - 95093 RMVar_ID_95093 Human_SNP_ID_590102830 m1A Human chr15 + 100887617 100887617 100887617 AGGCTGTGGAGGCTGCACAGGTTGCCTTCCAGAGGGGCTCGCCATGGCGCCGGCTGGATGCCCTG AGGCTGTGGAGGCTGCACAGGTTGCCTTCCAGGGGGGCTCGCCATGGCGCCGGCTGGATGCCCTG A G ALDH1A3 Ensembl:ENSG00000184254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:100885369..100892075 32194978 MeRIP-seq:(Medium) rs369355060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1650834,Human_Splice_Rec_1650835,Human_Splice_Rec_1650842,Human_Splice_Rec_1650843,Human_Splice_Rec_1650852,Human_Splice_Rec_1650853,Human_Splice_Rec_1650876,Human_Splice_Rec_1650877,Human_Splice_Rec_1650882,Human_Splice_Rec_1650883 95094 RMVar_ID_95094 Human_SNP_ID_590104344 m1A Human chr15 + 100893992 100893992 100893992 TTCCCCCTGCTGATGCTGGTGTGGAAGCTGGCACCCGCCCTCTGCTGTGGGAACACCATGGTCCT TTCCCCCTGCTGATGCTGGTGTGGAAGCTGGCGCCCGCCCTCTGCTGTGGGAACACCATGGTCCT A G ALDH1A3 Ensembl:ENSG00000184254 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:100892593..100893995 32194978 MeRIP-seq:(Medium) rs1436859231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1650846,Human_Splice_Rec_1650847,Human_Splice_Rec_1650858,Human_Splice_Rec_1650859 95095 RMVar_ID_95095 Human_SNP_ID_590109491 m1A Human chr15 + 100915073 100915072 100915074 GGAGACAGTGAGATACTCAGGGCGTTGTTAACAGGGAGTGGTATTTGAAGTGTCCAGCAGTTGCT GGAGACAGTGAGATACTCAGGGCGTTGTTAAC__GGAGTGGTATTTGAAGTGTCCAGCAGTTGCT CAG C ALDH1A3 Ensembl:ENSG00000184254 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:100908417..100915084 32194978 MeRIP-seq:(Medium) rs1199828445 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_123672 Human_miRNA_ID_975761 RMVar_hsa_circ_175200,RMVar_hsa_circ_91021 95096 RMVar_ID_95096 Human_SNP_ID_590171994 m1A Human chr15 - 101141855 101141855 101141855 ATGGGTGTGGGGGTAGATAGATGGTTGGGTGGATGGGTAGATAGGTGGATAGGCAGATGAGTGGG ATGGGTGTGGGGGTAGATAGATGGTTGGGTGGCTGGGTAGATAGGTGGATAGGCAGATGAGTGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101141816..101141887 26863196 MeRIP-seq:(Medium) rs1411439943 Functional Loss SNV dbSNP153 33..33 33 - - - 95097 RMVar_ID_95097 Human_SNP_ID_590183918 m1A Human chr15 - 101185445 101185445 101185445 AGGATGGAGGGTGCTCCATGGAGAGTGTTCACAGGGAAGGAGGATGGAGGGTGCTCCATGGAGGT AGGATGGAGGGTGCTCCATGGAGAGTGTTCACTGGGAAGGAGGATGGAGGGTGCTCCATGGAGGT T A CHSY1 Ensembl:ENSG00000131873 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101185443..101185643 26863196 MeRIP-seq:(Medium) rs941569807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342500,Human_RBP_ID_8182725,Human_RBP_ID_9048791 RMVar_hsa_circ_175219 95098 RMVar_ID_95098 Human_SNP_ID_590183919 m1A Human chr15 - 101185445 101185445 101185445 AGGATGGAGGGTGCTCCATGGAGAGTGTTCACAGGGAAGGAGGATGGAGGGTGCTCCATGGAGGT AGGATGGAGGGTGCTCCATGGAGAGTGTTCACGGGGAAGGAGGATGGAGGGTGCTCCATGGAGGT T C CHSY1 Ensembl:ENSG00000131873 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101185443..101185643 26863196 MeRIP-seq:(Medium) rs941569807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342500,Human_RBP_ID_8182725,Human_RBP_ID_9048791 RMVar_hsa_circ_175219 95099 RMVar_ID_95099 Human_SNP_ID_590194259 m1A Human chr15 + 101224727 101224727 101224727 TGCTAATACTTCACGTCCACACACACGCTTACACTTCTAAACCTTACACTTCACCTCCGACTTTC TGCTAATACTTCACGTCCACACACACGCTTACCCTTCTAAACCTTACACTTCACCTCCGACTTTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101224724..101224827 26863196 MeRIP-seq:(Medium) rs1474879106 Functional Loss SNV dbSNP153 33..33 33 - - - 95100 RMVar_ID_95100 Human_SNP_ID_590194735 m1A Human chr15 + 101226526 101226526 101226526 TCAGGCCTATTTGTGCCCAAACCAATGTCCTCAGCATTCCCTGCCTCCCCTCAACTCTGATGCCA TCAGGCCTATTTGTGCCCAAACCAATGTCCTCGGCATTCCCTGCCTCCCCTCAACTCTGATGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101226524..101226707 26863196 MeRIP-seq:(Medium) rs180776103 Functional Loss SNV dbSNP153 33..33 33 - - - 95101 RMVar_ID_95101 Human_SNP_ID_590194746 m1A Human chr15 + 101226580 101226580 101226580 CTCTGATGCCATCTGGCCTTACCCTTCGCCCCACTCTGCCTCGTCACTCCACTCATGCTGGCCAC CTCTGATGCCATCTGGCCTTACCCTTCGCCCCGCTCTGCCTCGTCACTCCACTCATGCTGGCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:101226577..101226671 26863196 MeRIP-seq:(Medium) rs569272626 Functional Loss SNV dbSNP153 33..33 33 - - - 95102 RMVar_ID_95102 Human_SNP_ID_590197001 m1A Human chr15 - 101235185 101235185 101235185 GAGCCGGGAGGTGCTTCGGAGAATGGTGCCGCACATTGGCAAGTGTCTCCGGGAGATGTACACCA GAGCCGGGAGGTGCTTCGGAGAATGGTGCCGCGCATTGGCAAGTGTCTCCGGGAGATGTACACCA T C CHSY1 Ensembl:ENSG00000131873 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101235138..101235308 26863196 MeRIP-seq:(Medium) rs1480921610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_455036,Human_RBP_ID_23645484 Human_miRNA_ID_2077157 RMVar_hsa_circ_175221,RMVar_hsa_circ_269838 95103 RMVar_ID_95103 Human_SNP_ID_590202200 m1A Human chr15 - 101251641 101251640 101251641 GCCGCGGCGGCGGGGGCGGGCGTGCGGAACAAAGCGCCGGCGCGGGGCCTGCGGGCGGCTCGGGG GCCGCGGCGGCGGGGGCGGGCGTGCGGAACAA_GCGCCGGCGCGGGGCCTGCGGGCGGCTCGGGG CT C CHSY1 Ensembl:ENSG00000131873 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:101251537..101251735 26863196 MeRIP-seq:(Medium) rs1268634568 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4342504 95104 RMVar_ID_95104 Human_SNP_ID_590202201 m1A Human chr15 - 101251643 101251643 101251643 AGGCCGCGGCGGCGGGGGCGGGCGTGCGGAACAAAGCGCCGGCGCGGGGCCTGCGGGCGGCTCGG AGGCCGCGGCGGCGGGGGCGGGCGTGCGGAACGAAGCGCCGGCGCGGGGCCTGCGGGCGGCTCGG T C CHSY1 Ensembl:ENSG00000131873 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:101251610..101251938 26863196 MeRIP-seq:(Medium) rs1041086190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4315867 95105 RMVar_ID_95105 Human_SNP_ID_590202289 m1A Human chr15 - 101251826 101251826 101251826 GAACCGAGCCCAGCCAGCCGGAGGACGCGGGCAGGGCGGGACGGGAGCCCGGACTCGTCTGCCGC GAACCGAGCCCAGCCAGCCGGAGGACGCGGGCGGGGCGGGACGGGAGCCCGGACTCGTCTGCCGC T C CHSY1 Ensembl:ENSG00000131873 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:101251816..101251944 26863196 MeRIP-seq:(Medium) rs1295857491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343454,Human_RBP_ID_5179200,Human_RBP_ID_22440210 95106 RMVar_ID_95106 Human_SNP_ID_590202309 m1A Human chr15 + 101251911 101251911 101251911 CTCTTCGTAGCCGGCGCCGCCGCCGCAGCTGCACATCCTCCGGCTTAGCTCGCCATTGCAACAGG CTCTTCGTAGCCGGCGCCGCCGCCGCAGCTGCGCATCCTCCGGCTTAGCTCGCCATTGCAACAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:101251624..101251983;chr15:101235351..101251975 26863196 MeRIP-seq:(Medium) rs1272095108 Functional Loss SNV dbSNP153 33..33 33 - - - 95107 RMVar_ID_95107 Human_SNP_ID_590202313 m1A Human chr15 - 101251917 101251917 101251917 GGGGCTCCTGTTGCAATGGCGAGCTAAGCCGGAGGATGTGCAGCTGCGGCGGCGGCGCCGGCTAC GGGGCTCCTGTTGCAATGGCGAGCTAAGCCGGGGGATGTGCAGCTGCGGCGGCGGCGCCGGCTAC T C CHSY1 Ensembl:ENSG00000131873 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:101251699..101251959 26863196 MeRIP-seq:(Medium) rs1283973526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886079,Human_RBP_ID_4343455,Human_RBP_ID_18418545 95108 RMVar_ID_95108 Human_SNP_ID_590202314 m1A Human chr15 - 101251917 101251917 101251917 GGGGCTCCTGTTGCAATGGCGAGCTAAGCCGGAGGATGTGCAGCTGCGGCGGCGGCGCCGGCTAC GGGGCTCCTGTTGCAATGGCGAGCTAAGCCGGCGGATGTGCAGCTGCGGCGGCGGCGCCGGCTAC T G CHSY1 Ensembl:ENSG00000131873 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:101251699..101251959 26863196 MeRIP-seq:(Medium) rs1283973526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886079,Human_RBP_ID_4343455,Human_RBP_ID_18418545 95109 RMVar_ID_95109 Human_SNP_ID_590209498 m1A Human chr15 - 101276677 101276677 101276677 TTTTTAGTTTTTTGAAAACTGTTTTTCTTTTCAGTGGGCTCCCTGCTGGCCACCTATGGCTGGTA TTTTTAGTTTTTTGAAAACTGTTTTTCTTTTCGGTGGGCTCCCTGCTGGCCACCTATGGCTGGTA T C SELENOS Ensembl:ENSG00000131871 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:101276601..101276730 26863410 MeRIP-seq:(Medium) rs756199410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343642,Human_RBP_ID_12477826 95110 RMVar_ID_95110 Human_SNP_ID_590209862 m1A Human chr15 - 101277406 101277406 101277406 GCGGCGGCGGCGGCGGCGGTCATGGAACGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA GCGGCGGCGGCGGCGGCGGTCATGGAACGCCAGGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA T C SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:101277323..101277454 26863196 MeRIP-seq:(Medium) rs1210366614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759941,Human_RBP_ID_1129685,Human_RBP_ID_1503288,Human_RBP_ID_4315916,Human_RBP_ID_5464618,Human_RBP_ID_9371963 Human_Splice_Rec_1651193,Human_Splice_Rec_1651223,Human_Splice_Rec_1651243,Human_Splice_Rec_1651249,Human_Splice_Rec_1651253 95111 RMVar_ID_95111 Human_SNP_ID_590209863 m1A Human chr15 - 101277406 101277406 101277406 GCGGCGGCGGCGGCGGCGGTCATGGAACGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA GCGGCGGCGGCGGCGGCGGTCATGGAACGCCACGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA T G SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:101277323..101277454 26863196 MeRIP-seq:(Medium) rs1210366614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759941,Human_RBP_ID_1129685,Human_RBP_ID_1503288,Human_RBP_ID_4315916,Human_RBP_ID_5464618,Human_RBP_ID_9371963 Human_Splice_Rec_1651193,Human_Splice_Rec_1651223,Human_Splice_Rec_1651243,Human_Splice_Rec_1651249,Human_Splice_Rec_1651253 95112 RMVar_ID_95112 Human_SNP_ID_590209864 m1A Human chr15 - 101277407 101277407 101277407 GGCGGCGGCGGCGGCGGCGGTCATGGAACGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGG GGCGGCGGCGGCGGCGGCGGTCATGGAACGCCGAGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGG T C SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101277301..101277475 26863196 MeRIP-seq:(Medium) rs1278528868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759941,Human_RBP_ID_1129685,Human_RBP_ID_1503288,Human_RBP_ID_4315916,Human_RBP_ID_5464618,Human_RBP_ID_9371963 Human_Splice_Rec_1651193,Human_Splice_Rec_1651223,Human_Splice_Rec_1651243,Human_Splice_Rec_1651249,Human_Splice_Rec_1651253 95113 RMVar_ID_95113 Human_SNP_ID_590209870 m1A Human chr15 - 101277412 101277412 101277412 GGCTGGGCGGCGGCGGCGGCGGCGGTCATGGAACGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGC GGCTGGGCGGCGGCGGCGGCGGCGGTCATGGACCGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGC T G SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:101277333..101277475;chr15:101277307..101277475 26863196 MeRIP-seq:(Medium) rs1475021338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759941,Human_RBP_ID_1129685,Human_RBP_ID_1503288,Human_RBP_ID_4315917,Human_RBP_ID_5464618,Human_RBP_ID_9371963 Human_Splice_Rec_1651193,Human_Splice_Rec_1651223,Human_Splice_Rec_1651243,Human_Splice_Rec_1651249,Human_Splice_Rec_1651253 95114 RMVar_ID_95114 Human_SNP_ID_590214988 m1A Human chr15 + 101295081 101295081 101295081 GCGGCTCGGTGCCGCCTGGGGACTGGCCGCCCACGCCCCCGGACTCACCCCGGAGGTCCAGCTCC GCGGCTCGGTGCCGCCTGGGGACTGGCCGCCCTCGCCCCCGGACTCACCCCGGAGGTCCAGCTCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:101295076..101295200 26863410 MeRIP-seq:(Medium) rs1434516357 Functional Loss SNV dbSNP153 33..33 33 - - - 95115 RMVar_ID_95115 Human_SNP_ID_590217691 m1A Human chr15 - 101304722 101304722 101304722 AGACTATAAATAAGATAGGTTTGAGGGCATAAAATGTATGACCACTGGGGCCGGAGTATCTATTT AGACTATAAATAAGATAGGTTTGAGGGCATAAGATGTATGACCACTGGGGCCGGAGTATCTATTT T C PCSK6 Ensembl:ENSG00000140479 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:101304679..101304781 32194978 MeRIP-seq:(Medium) rs1183245753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17857799,Human_RBP_ID_27230420 RMVar_hsa_circ_175229 95116 RMVar_ID_95116 Human_SNP_ID_590259647 m1A Human chr15 + 101459488 101459446 101459489 CCACCATTCCCGTCCCCCCACCCTAAGTCCACACCACCCGCTGCCACCGTTCCCGTCCCCCCACC __________________________________CACCCGCTGCCACCGTTCCCGTCCCCCCACC TCACCTGCTGCCACCATTCCCGTCCCCCCACCCTAAGTCCACAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101459360..101459688 26863196 MeRIP-seq:(Medium) rs370077435 Functional Loss DEL dbSNP153 1..34 33 - - - 95117 RMVar_ID_95117 Human_SNP_ID_590259694 m1A Human chr15 + 101459488 101459487 101459488 CCACCATTCCCGTCCCCCCACCCTAAGTCCACACCACCCGCTGCCACCGTTCCCGTCCCCCCACC CCACCATTCCCGTCCCCCCACCCTAAGTCCAC_CCACCCGCTGCCACCGTTCCCGTCCCCCCACC CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101459360..101459688 26863196 MeRIP-seq:(Medium) rs1241835385 Functional Loss DEL dbSNP153 33..33 33 - - - 95118 RMVar_ID_95118 Human_SNP_ID_590259701 m1A Human chr15 + 101459491 101459491 101459491 CCATTCCCGTCCCCCCACCCTAAGTCCACACCACCCGCTGCCACCGTTCCCGTCCCCCCACCCTA CCATTCCCGTCCCCCCACCCTAAGTCCACACCCCCCGCTGCCACCGTTCCCGTCCCCCCACCCTA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:101459253..101459819 26863196 MeRIP-seq:(Medium) rs1182750268 Functional Loss SNV dbSNP153 33..33 33 - - - 95119 RMVar_ID_95119 Human_SNP_ID_590259897 m1A Human chr15 + 101460074 101460074 101460074 GCCCCACACTGAACTGAGGGCCTCCTCCCCACACAGCCACATGGCCACCACTATGCCCCTATGAA GCCCCACACTGAACTGAGGGCCTCCTCCCCACCCAGCCACATGGCCACCACTATGCCCCTATGAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101460064..101460219 26863196 MeRIP-seq:(Medium) rs139183540 Functional Loss SNV dbSNP153 33..33 33 - - - 95120 RMVar_ID_95120 Human_SNP_ID_590263638 m1A Human chr15 - 101474829 101474829 101474829 AGGGTGTTGAGGTACCCGGGGACTGGGTAGGCAGTGGTGGGGAGCTGCTGCAGGGATGGAGGCAA AGGGTGTTGAGGTACCCGGGGACTGGGTAGGCGGTGGTGGGGAGCTGCTGCAGGGATGGAGGCAA T C PCSK6 Ensembl:ENSG00000140479 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101474784..101474883 26863196 MeRIP-seq:(Medium) rs1354797008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21970019 95121 RMVar_ID_95121 Human_SNP_ID_590267911 m1A Human chr15 - 101489420 101489420 101489420 CTGGGCGGTGCAAGTGCTGGGCGGCCCGGCCGAGGCGGACCGCGTGGCGGCGGCGCACGGGTACC CTGGGCGGTGCAAGTGCTGGGCGGCCCGGCCGGGGCGGACCGCGTGGCGGCGGCGCACGGGTACC T C PCSK6 Ensembl:ENSG00000140479 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:101489341..101489541 26863196 MeRIP-seq:(Medium) rs1414788967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342511,Human_RBP_ID_9324447 Human_Splice_Rec_1651445,Human_Splice_Rec_1651487,Human_Splice_Rec_1651563,Human_Splice_Rec_1651601,Human_Splice_Rec_1651649,Human_Splice_Rec_1651677,Human_Splice_Rec_1651707,Human_Splice_Rec_1651737 Human_miRNA_ID_2391846 95122 RMVar_ID_95122 Human_SNP_ID_590267971 m1A Human chr15 + 101489497 101489497 101489497 ACGGGGCGCGGCGGGGGCGCGGAGCAGGCGGCAGGCAGCGCCAGCAGCAGCAGCCAGCGCCAGGG ACGGGGCGCGGCGGGGGCGCGGAGCAGGCGGCGGGCAGCGCCAGCAGCAGCAGCCAGCGCCAGGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:101489492..101489802 26863410 MeRIP-seq:(Medium) rs1326349493 Functional Loss SNV dbSNP153 33..33 33 - - - 95123 RMVar_ID_95123 Human_SNP_ID_590268062 m1A Human chr15 - 101489670 101489670 101489670 CAGCTCGGGCGCCGCGCGAGCCTGTCGCCGCTATGCCTCCGCGCGCGCCGCCTGCGCCCGGGCCC CAGCTCGGGCGCCGCGCGAGCCTGTCGCCGCTGTGCCTCCGCGCGCGCCGCCTGCGCCCGGGCCC T C PCSK6 Ensembl:ENSG00000140479 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:101489620..101489692 26863196 MeRIP-seq:(Medium) rs1475787959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489272,Human_RBP_ID_4342514,Human_RBP_ID_9324649 Human_miRNA_ID_2476119,Human_miRNA_ID_2961904 95124 RMVar_ID_95124 Human_SNP_ID_590312587 m1A Human chr15 + 101652322 101652322 101652322 GAACTGCGAGAGGAAGAGCAGCACGCGACACAAGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC GAACTGCGAGAGGAAGAGCAGCACGCGACACACGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101652194..101652324 26863196 MeRIP-seq:(Medium) rs11538412 Functional Loss SNV dbSNP153 33..33 33 - - - 95125 RMVar_ID_95125 Human_SNP_ID_590312588 m1A Human chr15 + 101652322 101652322 101652322 GAACTGCGAGAGGAAGAGCAGCACGCGACACAAGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC GAACTGCGAGAGGAAGAGCAGCACGCGACACAGGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101652194..101652324 26863196 MeRIP-seq:(Medium) rs11538412 Functional Loss SNV dbSNP153 33..33 33 - - - 95126 RMVar_ID_95126 Human_SNP_ID_590312589 m1A Human chr15 + 101652322 101652322 101652322 GAACTGCGAGAGGAAGAGCAGCACGCGACACAAGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC GAACTGCGAGAGGAAGAGCAGCACGCGACACATGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:101652194..101652324 26863196 MeRIP-seq:(Medium) rs11538412 Functional Loss SNV dbSNP153 33..33 33 - - - 95127 RMVar_ID_95127 Human_SNP_ID_590312602 m1A Human chr15 + 101652330 101652330 101652330 AGAGGAAGAGCAGCACGCGACACAAGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTCCCGCCATC AGAGGAAGAGCAGCACGCGACACAAGGCGCGGCGGCCCCTCAGCGGGAGCACCCCTCCCGCCATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:101652199..101652334;chr15:101652194..101652334;chr15:101652176..101652329 26863196 MeRIP-seq:(Medium) rs747787074 Functional Loss SNV dbSNP153 33..33 33 - - - 95128 RMVar_ID_95128 Human_SNP_ID_590312603 m1A Human chr15 + 101652330 101652330 101652330 AGAGGAAGAGCAGCACGCGACACAAGGCGCGGAGGCCCCTCAGCGGGAGCACCCCTCCCGCCATC AGAGGAAGAGCAGCACGCGACACAAGGCGCGGGGGCCCCTCAGCGGGAGCACCCCTCCCGCCATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:101652199..101652334;chr15:101652194..101652334;chr15:101652176..101652329 26863196 MeRIP-seq:(Medium) rs747787074 Functional Loss SNV dbSNP153 33..33 33 - - - 95129 RMVar_ID_95129 Human_SNP_ID_590400910 m1A Human chr15 + 101973964 101973964 101973964 GACCTGGGCCAGGTGCCTGAGATTGATGTTCCATCCTACCTGCCTGACCTGCCCGGCATTACCAA GACCTGGGCCAGGTGCCTGAGATTGATGTTCCCTCCTACCTGCCTGACCTGCCCGGCATTACCAA A C WASH3P Ensembl:ENSG00000185596 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1240910256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27810705 Human_Splice_Rec_1652118,Human_Splice_Rec_1652128,Human_Splice_Rec_1652146,Human_Splice_Rec_1652164 95130 RMVar_ID_95130 Human_SNP_ID_590400911 m1A Human chr15 + 101973964 101973964 101973964 GACCTGGGCCAGGTGCCTGAGATTGATGTTCCATCCTACCTGCCTGACCTGCCCGGCATTACCAA GACCTGGGCCAGGTGCCTGAGATTGATGTTCCGTCCTACCTGCCTGACCTGCCCGGCATTACCAA A G WASH3P Ensembl:ENSG00000185596 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1240910256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27810705 Human_Splice_Rec_1652118,Human_Splice_Rec_1652128,Human_Splice_Rec_1652146,Human_Splice_Rec_1652164 95131 RMVar_ID_95131 Human_SNP_ID_590401351 m1A Human chr15 + 101975117 101975117 101975117 CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAG CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCGTGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAG A G WASH3P Ensembl:ENSG00000185596 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs755525291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759805,Human_RBP_ID_814595,Human_RBP_ID_886390,Human_RBP_ID_1511714,Human_RBP_ID_3946831,Human_RBP_ID_5567318,Human_RBP_ID_8804242,Human_RBP_ID_17484650,Human_RBP_ID_18161609,Human_RBP_ID_18981875,Human_RBP_ID_21970673,Human_RBP_ID_26768823 Human_Splice_Rec_1652133,Human_Splice_Rec_1652151,Human_Splice_Rec_1652169 95132 RMVar_ID_95132 Human_SNP_ID_590401352 m1A Human chr15 + 101975117 101975117 101975117 CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAG CTGGGGGCATCGGCAAGGCCAAGCTGCGCAGCTTGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAG A T WASH3P Ensembl:ENSG00000185596 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs755525291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759805,Human_RBP_ID_814595,Human_RBP_ID_886390,Human_RBP_ID_1511714,Human_RBP_ID_3946831,Human_RBP_ID_5567318,Human_RBP_ID_8804242,Human_RBP_ID_17484650,Human_RBP_ID_18161609,Human_RBP_ID_18981875,Human_RBP_ID_21970673,Human_RBP_ID_26768823 Human_Splice_Rec_1652133,Human_Splice_Rec_1652151,Human_Splice_Rec_1652169 95133 RMVar_ID_95133 Human_SNP_ID_590401372 m1A Human chr15 + 101975148 101975147 101975149 CATGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAGAAGGAGCAGGAGCAAGGTGAGCGGGCCCTGG CATGAAGGAGCGAAAGCTGGAGAAGAAGCAGC__AAGGAGCAGGAGCAAGGTGAGCGGGCCCTGG CAG C WASH3P Ensembl:ENSG00000185596 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:101975125..101975202 26863196 MeRIP-seq:(Medium) rs778284493 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_814596,Human_RBP_ID_886390,Human_RBP_ID_1511714,Human_RBP_ID_3945948,Human_RBP_ID_5567318,Human_RBP_ID_5646484,Human_RBP_ID_8183511,Human_RBP_ID_8251541,Human_RBP_ID_8804242,Human_RBP_ID_17673214,Human_RBP_ID_18161609,Human_RBP_ID_18981875,Human_RBP_ID_26768823 Human_Splice_Rec_1652133,Human_Splice_Rec_1652151,Human_Splice_Rec_1652169 95134 RMVar_ID_95134 Human_SNP_ID_601435646 m1A Human chr16 - 46618350 46618350 46618350 TTTTTTTTAGGTTTGTTCCAAGATGAAGATTCATGCAGTGATTGTAGCTACCGTGATAAACCAGG TTTTTTTTAGGTTTGTTCCAAGATGAAGATTCGTGCAGTGATTGTAGCTACCGTGATAAACCAGG T C SHCBP1 Ensembl:ENSG00000171241 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:46618226..46618416;chr16:46618226..46620527 26863196 MeRIP-seq:(Medium) rs148413248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888715,Human_RBP_ID_1518511,Human_RBP_ID_1842606,Human_RBP_ID_12738807 Human_Splice_Rec_1707896,Human_Splice_Rec_1707936 Human_miRNA_ID_2235259,Human_miRNA_ID_3029425 RMVar_hsa_circ_362364,RMVar_hsa_circ_4165,RMVar_hsa_circ_65929,RMVar_hsa_circ_99175,RMVar_hsa_circ_276238,RMVar_hsa_circ_337326,RMVar_hsa_circ_178078,RMVar_hsa_circ_178079 95135 RMVar_ID_95135 Human_SNP_ID_601435650 m1A Human chr16 - 46618362 46618362 46618362 TATTTTTGCTTTTTTTTTTTAGGTTTGTTCCAAGATGAAGATTCATGCAGTGATTGTAGCTACCG TATTTTTGCTTTTTTTTTTTAGGTTTGTTCCAGGATGAAGATTCATGCAGTGATTGTAGCTACCG T C SHCBP1 Ensembl:ENSG00000171241 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr16:46618276..46620527;chr16:46618251..46620527 26863196 MeRIP-seq:(Medium) rs748113923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888715,Human_RBP_ID_12738810 Human_Splice_Rec_1707896,Human_Splice_Rec_1707936 Human_miRNA_ID_2235259,Human_miRNA_ID_3029425 RMVar_hsa_circ_362364,RMVar_hsa_circ_4165,RMVar_hsa_circ_65929,RMVar_hsa_circ_99175,RMVar_hsa_circ_276238,RMVar_hsa_circ_337326,RMVar_hsa_circ_178078,RMVar_hsa_circ_178079 95136 RMVar_ID_95136 Human_SNP_ID_601463030 m1A Human chr16 - 46730095 46730095 46730095 GTGCAGGATGGCCTCAGTGGTGTGGGGTGAGGAGATGTTCCCTGGGGTGCAGGATGGCCTGGGTG GTGCAGGATGGCCTCAGTGGTGTGGGGTGAGGGGATGTTCCCTGGGGTGCAGGATGGCCTGGGTG T C MYLK3 Ensembl:ENSG00000140795 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:46730093..46730567 26863196 MeRIP-seq:(Medium) rs1017332144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37357,RMVar_hsa_circ_44432 95137 RMVar_ID_95137 Human_SNP_ID_601463228 m1A Human chr16 - 46730693 46730693 46730693 CACAGGTCCTTATTGCCTCCTGAGCAGATGACAGTCCGGCCCCACCAGCTCCTTTTGAACACCGG CACAGGTCCTTATTGCCTCCTGAGCAGATGACGGTCCGGCCCCACCAGCTCCTTTTGAACACCGG T C MYLK3 Ensembl:ENSG00000140795 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46730069..46730737 26863196 MeRIP-seq:(Medium) rs1165889514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1708182,Human_Splice_Rec_1708204,Human_Splice_Rec_1708234 RMVar_hsa_circ_37357,RMVar_hsa_circ_44432 95138 RMVar_ID_95138 Human_SNP_ID_601467745 m1A Human chr16 + 46748003 46748003 46748003 GGCCCGGTGCCCGGGAGGCCTCCAGCCTGTGCAGGCCCCGCTCCAGGTGGCCCATGTCTCGGCAC GGCCCGGTGCCCGGGAGGCCTCCAGCCTGTGCGGGCCCCGCTCCAGGTGGCCCATGTCTCGGCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46747954..46748154 26863196 MeRIP-seq:(Medium) rs1313770426 Functional Loss SNV dbSNP153 33..33 33 - - - 95139 RMVar_ID_95139 Human_SNP_ID_601467844 m1A Human chr16 - 46748270 46748270 46748270 TGTCAGCTACGGAGGACAATGACCTTGCAGACACCACCGCCTGAGTGAGAACCAGGGGTCTGTGC TGTCAGCTACGGAGGACAATGACCTTGCAGACTCCACCGCCTGAGTGAGAACCAGGGGTCTGTGC T A MYLK3 Ensembl:ENSG00000140795 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46748220..46748332 26863196 MeRIP-seq:(Medium) rs192142624 Functional Loss SNV dbSNP153 33..33 33 - - - 95140 RMVar_ID_95140 Human_SNP_ID_601486802 m1A Human chr16 + 46831082 46831082 46831082 CCGCCCGCCCGCGCGCCCGGCCCCCGGCACCCACCTGTTGGTCGCACTCGGGGCATGATTTGGTG CCGCCCGCCCGCGCGCCCGGCCCCCGGCACCCCCCTGTTGGTCGCACTCGGGGCATGATTTGGTG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:46831040..46831193 26863196 MeRIP-seq:(Medium) rs1360895007 Functional Loss SNV dbSNP153 33..33 33 - - - 95141 RMVar_ID_95141 Human_SNP_ID_601504285 m1A Human chr16 + 46903964 46903964 46903964 AGAGCTTAAGGGGAAACGTGGCATTCACGCTCATGGGGAGGATGAGTAAGAACCTGCAAATGCAT AGAGCTTAAGGGGAAACGTGGCATTCACGCTCCTGGGGAGGATGAGTAAGAACCTGCAAATGCAT A C GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46903962..46904064 26863196 MeRIP-seq:(Medium) rs1208165662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12740448,Human_RBP_ID_23689784 RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_287310,RMVar_hsa_circ_326819,RMVar_hsa_circ_373404,RMVar_hsa_circ_178112,RMVar_hsa_circ_178114,RMVar_hsa_circ_344182,RMVar_hsa_circ_332278 95142 RMVar_ID_95142 Human_SNP_ID_601504413 m1A Human chr16 + 46904516 46904516 46904516 TCTTTAGGGCAGGCCTCCGGGAGACAGACTAGAAATGAGCCTAGAAGGATCAGTGTGGTTTGGAG TCTTTAGGGCAGGCCTCCGGGAGACAGACTAGGAATGAGCCTAGAAGGATCAGTGTGGTTTGGAG A G GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:46904514..46904621 26863196 MeRIP-seq:(Medium) rs1407385371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12740460 RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_287310,RMVar_hsa_circ_326819,RMVar_hsa_circ_373404,RMVar_hsa_circ_178112,RMVar_hsa_circ_178114,RMVar_hsa_circ_344182,RMVar_hsa_circ_332278 95143 RMVar_ID_95143 Human_SNP_ID_601507085 m1A Human chr16 - 46915482 46915480 46915482 TAGGTGTGTTGGGGTGTCTGTGTATGGTGTGTAATGTGTGTGCAGGTGTGGTGGGGTGTGTGTGT TAGGTGTGTTGGGGTGTCTGTGTATGGTGTGT__TGTGTGTGCAGGTGTGGTGGGGTGTGTGTGT ATT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46915480..46915545 26863196 MeRIP-seq:(Medium) rs1250999648 Functional Loss DEL dbSNP153 33..34 33 - - - 95144 RMVar_ID_95144 Human_SNP_ID_601507089 m1A Human chr16 - 46915482 46915482 46915482 TAGGTGTGTTGGGGTGTCTGTGTATGGTGTGTAATGTGTGTGCAGGTGTGGTGGGGTGTGTGTGT TAGGTGTGTTGGGGTGTCTGTGTATGGTGTGTGATGTGTGTGCAGGTGTGGTGGGGTGTGTGTGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46915480..46915545 26863196 MeRIP-seq:(Medium) rs1184155630 Functional Loss SNV dbSNP153 33..33 33 - - - 95145 RMVar_ID_95145 Human_SNP_ID_601511050 m1A Human chr16 + 46930165 46930164 46930165 CTTCCGGCTCCCCTCCCAGGCTGCAGACTCTGACCTGTGGCATCAGGCTTCTCCCAGTACAGGAG CTTCCGGCTCCCCTCCCAGGCTGCAGACTCTG_CCTGTGGCATCAGGCTTCTCCCAGTACAGGAG GA G GPT2 Ensembl:ENSG00000166123 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:46929956..46930205 32194978 MeRIP-seq:(Medium) rs758295196 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6514427,Human_RBP_ID_9062336,Human_RBP_ID_12740778,Human_RBP_ID_27442928 RMVar_hsa_circ_127742,RMVar_hsa_circ_178118,RMVar_hsa_circ_99044,RMVar_hsa_circ_178123 95146 RMVar_ID_95146 Human_SNP_ID_601519585 m1A Human chr16 - 46964674 46964674 46964674 CATGGACAGAGAATTACATTCACTGGGGAAGCAGACCAGGCCCCAGGAGTGGAACCCGGAGACAT CATGGACAGAGAATTACATTCACTGGGGAAGCCGACCAGGCCCCAGGAGTGGAACCCGGAGACAT T G DNAJA2 Ensembl:ENSG00000069345 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:46964601..46964675 26863196 MeRIP-seq:(Medium) rs769651421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4370117,Human_RBP_ID_6514539,Human_RBP_ID_12740984,Human_RBP_ID_22442019 Human_Splice_Rec_1708347,Human_Splice_Rec_1708363 Human_miRNA_ID_2040906,Human_miRNA_ID_2708957,Human_miRNA_ID_3019890 RMVar_hsa_circ_120220,RMVar_hsa_circ_178128,RMVar_hsa_circ_24687,RMVar_hsa_circ_299104,RMVar_hsa_circ_4706,RMVar_hsa_circ_37170,RMVar_hsa_circ_98672,RMVar_hsa_circ_178129,RMVar_hsa_circ_19704,RMVar_hsa_circ_360406,RMVar_hsa_circ_363387,RMVar_hsa_circ_178130 95147 RMVar_ID_95147 Human_SNP_ID_601522153 m1A Human chr16 + 46973620 46973620 46973620 AGTGCTCGGGGAGAAGGTGGCGAAGCAGACAGAGCGGAGTCGGGCCCACAAGCGGCGTCGGCGGC AGTGCTCGGGGAGAAGGTGGCGAAGCAGACAGGGCGGAGTCGGGCCCACAAGCGGCGTCGGCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46973454..46973700 26863196 MeRIP-seq:(Medium) rs1415118132 Functional Loss SNV dbSNP153 33..33 33 - - - 95148 RMVar_ID_95148 Human_SNP_ID_601563387 m1A Human chr16 + 47143675 47143662 47143676 GCTGAGGTAGCGGCGGCGGTGGCTCGGCGCTCACGGCTCGGCGCGGCGGCGACGGCCCCACTCCG GCTGAGGTAGCGGCGGCGGT______________GGCTCGGCGCGGCGGCGACGGCCCCACTCCG TGGCTCGGCGCTCAC T ITFG1-AS1 RNACentral:URS00009C1D3E lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:47143624..47143957 26863196 MeRIP-seq:(Medium) rs1009610379 Functional Loss DEL dbSNP153 21..34 33 - - - 95149 RMVar_ID_95149 Human_SNP_ID_601563462 m1A Human chr16 + 47143898 47143898 47143898 GAGGGCCGAGGAGTGCGGACGCGCGGCGCGGGACCGGCAGGCAGCTCCGCCCGCGGCCCCGGCGC GAGGGCCGAGGAGTGCGGACGCGCGGCGCGGGTCCGGCAGGCAGCTCCGCCCGCGGCCCCGGCGC A T ITFG1-AS1 RNACentral:URS00009C1D3E lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:47143797..47143947 26863410 MeRIP-seq:(Medium) rs990730970 Functional Loss SNV dbSNP153 33..33 33 - - - 95150 RMVar_ID_95150 Human_SNP_ID_601637682 m1A Human chr16 + 47460945 47460945 47460945 CGGCCCCAAAGAGCTCGGCCGTGACGTTGTGCAGCGCCCGCGCTGGGACCGGCCCGACTCCCAGT CGGCCCCAAAGAGCTCGGCCGTGACGTTGTGCCGCGCCCGCGCTGGGACCGGCCCGACTCCCAGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:47460943..47461049 26863196 MeRIP-seq:(Medium) rs1422507707 Functional Loss SNV dbSNP153 33..33 33 - - - 95151 RMVar_ID_95151 Human_SNP_ID_601637899 m1A Human chr16 + 47461331 47461331 47461331 ATTGCTGACAGGCGGCCCCGGGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGATGGCGGGGGCGG ATTGCTGACAGGCGGCCCCGGGGGCGGTGGCCGAGGCGGCGACCGGAGCGCGATGGCGGGGGCGG A G PHKB Ensembl:ENSG00000102893 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:47461322..47461456 26863196 MeRIP-seq:(Medium) rs748523564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4394703,Human_RBP_ID_5317559,Human_RBP_ID_22944653 Human_Splice_Rec_1708633,Human_Splice_Rec_1708647,Human_Splice_Rec_1708709,Human_Splice_Rec_1708769,Human_Splice_Rec_1708771,Human_Splice_Rec_1708773,Human_Splice_Rec_1708833,Human_Splice_Rec_1708853 RMVar_hsa_circ_178161,RMVar_hsa_circ_121637 95152 RMVar_ID_95152 Human_SNP_ID_601637916 m1A Human chr16 + 47461351 47461351 47461351 GGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGATGGCGGGGGCGGCGGGACTCACGGCAGAAGTG GGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGGTGGCGGGGGCGGCGGGACTCACGGCAGAAGTG A G PHKB Ensembl:ENSG00000102893 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:47461344..47461434 26863196 MeRIP-seq:(Medium) rs750315969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817318,Human_RBP_ID_4393823,Human_RBP_ID_5317559,Human_RBP_ID_18986264,Human_RBP_ID_22944441 Human_Splice_Rec_1708633,Human_Splice_Rec_1708647,Human_Splice_Rec_1708709,Human_Splice_Rec_1708769,Human_Splice_Rec_1708771,Human_Splice_Rec_1708773,Human_Splice_Rec_1708833,Human_Splice_Rec_1708853 RMVar_hsa_circ_178161,RMVar_hsa_circ_121637 95153 RMVar_ID_95153 Human_SNP_ID_601637917 m1A Human chr16 + 47461351 47461351 47461351 GGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGATGGCGGGGGCGGCGGGACTCACGGCAGAAGTG GGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGTTGGCGGGGGCGGCGGGACTCACGGCAGAAGTG A T PHKB Ensembl:ENSG00000102893 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:47461344..47461434 26863196 MeRIP-seq:(Medium) rs750315969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_817318,Human_RBP_ID_4393823,Human_RBP_ID_5317559,Human_RBP_ID_18986264,Human_RBP_ID_22944441 Human_Splice_Rec_1708633,Human_Splice_Rec_1708647,Human_Splice_Rec_1708709,Human_Splice_Rec_1708769,Human_Splice_Rec_1708771,Human_Splice_Rec_1708773,Human_Splice_Rec_1708833,Human_Splice_Rec_1708853 RMVar_hsa_circ_178161,RMVar_hsa_circ_121637 95154 RMVar_ID_95154 Human_SNP_ID_601637918 m1A Human chr16 - 47461352 47461352 47461352 TCACTTCTGCCGTGAGTCCCGCCGCCCCCGCCATCGCGCTCCGGTCGCCGCCTTGGCCACCGCCC TCACTTCTGCCGTGAGTCCCGCCGCCCCCGCCGTCGCGCTCCGGTCGCCGCCTTGGCCACCGCCC T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:47461351..47461605 26863196 MeRIP-seq:(Medium) rs766369800 Functional Loss SNV dbSNP153 33..33 33 - - - 95155 RMVar_ID_95155 Human_SNP_ID_601637935 m1A Human chr16 + 47461368 47461368 47461368 GGCGACCGGAGCGCGATGGCGGGGGCGGCGGGACTCACGGCAGAAGTGAGCTGGAAGGTCTTGGA GGCGACCGGAGCGCGATGGCGGGGGCGGCGGGTCTCACGGCAGAAGTGAGCTGGAAGGTCTTGGA A T PHKB Ensembl:ENSG00000102893 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:47461352..47461451 26863196 MeRIP-seq:(Medium) rs777322397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760749,Human_RBP_ID_817318,Human_RBP_ID_4393823,Human_RBP_ID_5317559,Human_RBP_ID_17669670,Human_RBP_ID_18679874,Human_RBP_ID_18986264,Human_RBP_ID_22944441 Human_Splice_Rec_1708633,Human_Splice_Rec_1708647,Human_Splice_Rec_1708709,Human_Splice_Rec_1708769,Human_Splice_Rec_1708771,Human_Splice_Rec_1708773,Human_Splice_Rec_1708833,Human_Splice_Rec_1708853 RMVar_hsa_circ_178161,RMVar_hsa_circ_121637 95156 RMVar_ID_95156 Human_SNP_ID_601647760 m1A Human chr16 - 47504814 47504814 47504814 GACTGGAGAGGCCTCGGGATCCCACCTCAGCCAGGGAGTGCGCTGGCCTTCACCTTCACTGCGCC GACTGGAGAGGCCTCGGGATCCCACCTCAGCCGGGGAGTGCGCTGGCCTTCACCTTCACTGCGCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:47504706..47504875 26863196 MeRIP-seq:(Medium) rs796670787 Functional Loss SNV dbSNP153 33..33 33 - - - 95157 RMVar_ID_95157 Human_SNP_ID_601825444 m1A Human chr16 - 48244356 48244354 48244356 GCTGGCAGCCTTTCGCACTGGGGGCTGTCAAAAAGAGCCAGACAGACAGCTGCCCCCGGCCTGCC GCTGGCAGCCTTTCGCACTGGGGGCTGTCAAA__GAGCCAGACAGACAGCTGCCCCCGGCCTGCC CTT C ABCC11 Ensembl:ENSG00000121270 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:48244305..48244505 26863196 MeRIP-seq:(Medium) rs1567300864 Functional Loss DEL dbSNP153 33..34 33 - - - 95158 RMVar_ID_95158 Human_SNP_ID_601825467 m1A Human chr16 + 48244389 48244389 48244389 TTTGACAGCCCCCAGTGCGAAAGGCTGCCAGCATGTCATCAGTGAGCCCCATCCAGATCCCCAGT TTTGACAGCCCCCAGTGCGAAAGGCTGCCAGCCTGTCATCAGTGAGCCCCATCCAGATCCCCAGT A C LONP2 Ensembl:ENSG00000102910 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:48244338..48244490 26863196 MeRIP-seq:(Medium) rs745524521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760776,Human_RBP_ID_4370721,Human_RBP_ID_9285773,Human_RBP_ID_26441458,Human_RBP_ID_26810328 RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220 95159 RMVar_ID_95159 Human_SNP_ID_601825468 m1A Human chr16 + 48244389 48244389 48244389 TTTGACAGCCCCCAGTGCGAAAGGCTGCCAGCATGTCATCAGTGAGCCCCATCCAGATCCCCAGT TTTGACAGCCCCCAGTGCGAAAGGCTGCCAGCGTGTCATCAGTGAGCCCCATCCAGATCCCCAGT A G LONP2 Ensembl:ENSG00000102910 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:48244338..48244490 26863196 MeRIP-seq:(Medium) rs745524521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760776,Human_RBP_ID_4370721,Human_RBP_ID_9285773,Human_RBP_ID_26441458,Human_RBP_ID_26810328 RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220 95160 RMVar_ID_95160 Human_SNP_ID_601846882 m1A Human chr16 + 48339182 48339182 48339182 GAGAGAAGAGGAGCCAACAAAGAAGTCGGGAAAAACAGAAAGGGACTGGGAAGGAACAAGCCTTC GAGAGAAGAGGAGCCAACAAAGAAGTCGGGAAGAACAGAAAGGGACTGGGAAGGAACAAGCCTTC A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:48339170..48339241 26863196 MeRIP-seq:(Medium) rs1407871862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_57064,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248,RMVar_hsa_circ_364069 95161 RMVar_ID_95161 Human_SNP_ID_601846960 m1A Human chr16 + 48339585 48339585 48339585 AGAATGTTTTCAAAATAGTAGCTGCTGCTGAGAGTAATCCAGTAGAGAGCACAGACTGATGTTGC AGAATGTTTTCAAAATAGTAGCTGCTGCTGAGGGTAATCCAGTAGAGAGCACAGACTGATGTTGC A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:48339582..48340170 26863196 MeRIP-seq:(Medium) rs1177532685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12744982 RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_57064,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248,RMVar_hsa_circ_364069 95162 RMVar_ID_95162 Human_SNP_ID_601850094 m1A Human chr16 + 48352513 48352513 48352513 AAAAATATACAGGCGTGTTAGCATGTGCCTGTAATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA AAAAATATACAGGCGTGTTAGCATGTGCCTGTGATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1129702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26441463 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 95163 RMVar_ID_95163 Human_SNP_ID_601850095 m1A Human chr16 + 48352513 48352513 48352513 AAAAATATACAGGCGTGTTAGCATGTGCCTGTAATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA AAAAATATACAGGCGTGTTAGCATGTGCCTGTTATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA A T LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1129702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26441463 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 95164 RMVar_ID_95164 Human_SNP_ID_601850298 m1A Human chr16 + 48353385 48353385 48353385 AAAATTAGCTGGGCATGGTGGCACCCGCCTGTAGTCCAGCTACTTGAGGCTGAGATGGGAGGATG AAAATTAGCTGGGCATGGTGGCACCCGCCTGTCGTCCAGCTACTTGAGGCTGAGATGGGAGGATG A C LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 95165 RMVar_ID_95165 Human_SNP_ID_601850299 m1A Human chr16 + 48353385 48353385 48353385 AAAATTAGCTGGGCATGGTGGCACCCGCCTGTAGTCCAGCTACTTGAGGCTGAGATGGGAGGATG AAAATTAGCTGGGCATGGTGGCACCCGCCTGTGGTCCAGCTACTTGAGGCTGAGATGGGAGGATG A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 95166 RMVar_ID_95166 Human_SNP_ID_601855658 m1A Human chr16 + 48373025 48373025 48373025 TACTCTTGGTTTTCCTATCTCAGTCACTCCTCAGCTTCCTTTTATTCCTGCTCTTCTCCCCCAAA TACTCTTGGTTTTCCTATCTCAGTCACTCCTCGGCTTCCTTTTATTCCTGCTCTTCTCCCCCAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:48373023..48373135 26863196 MeRIP-seq:(Medium) rs1021152416 Functional Loss SNV dbSNP153 33..33 33 - - - 95167 RMVar_ID_95167 Human_SNP_ID_601859128 m1A Human chr16 + 48385280 48385266 48385281 GCGCTCCGTCGCCAACCCCCGCCACCGCGGGCAGCGCCACCGCCTCTTCCCGGCGCCGAGACCGA GCGCTCCGTCGCCAACCCC_______________CGCCACCGCCTCTTCCCGGCGCCGAGACCGA CCGCCACCGCGGGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:48385116..48385474 26863196 MeRIP-seq:(Medium) rs1221204056 Functional Loss DEL dbSNP153 20..34 33 - - - 95168 RMVar_ID_95168 Human_SNP_ID_601904943 m1A Human chr16 - 48576711 48576711 48576711 ACATGACTTTGAAAAAGTAGGAAGGAGAAGGAAGTCATGAAAGGTAGAATTTTTAGATGAAATGG ACATGACTTTGAAAAAGTAGGAAGGAGAAGGATGTCATGAAAGGTAGAATTTTTAGATGAAATGG T A N4BP1 Ensembl:ENSG00000102921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:48576709..48576861 26863196 MeRIP-seq:(Medium) rs1367875809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89968,RMVar_hsa_circ_178255 95169 RMVar_ID_95169 Human_SNP_ID_601911379 m1A Human chr16 - 48603879 48603879 48603879 GGTCAGCCTTGTTCAAGCTAGGACAGGGAAACAGATGAGAGCAGAAAGGGCGGAGTGAGCTGCAA GGTCAGCCTTGTTCAAGCTAGGACAGGGAAACGGATGAGAGCAGAAAGGGCGGAGTGAGCTGCAA T C N4BP1 Ensembl:ENSG00000102921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:48603872..48603952 26863196 MeRIP-seq:(Medium) rs1251831905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6516838 RMVar_hsa_circ_89968,RMVar_hsa_circ_178255 95170 RMVar_ID_95170 Human_SNP_ID_601913147 m1A Human chr16 + 48610053 48610053 48610053 CCCCCTCAGCTTGCTGCCGCTGCTCCCAAGCCAGTCAGGCGGCGTCGGCCCTTCCCGGCCGCCTC CCCCCTCAGCTTGCTGCCGCTGCTCCCAAGCCGGTCAGGCGGCGTCGGCCCTTCCCGGCCGCCTC A G lnc-LONP2-9 RNACentral:URS00009B78C3 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:48609833..48610174 26863196 MeRIP-seq:(Medium) rs1340920157 Functional Loss SNV dbSNP153 33..33 33 - - - 95171 RMVar_ID_95171 Human_SNP_ID_602267339 m1A Human chr16 + 50025266 50025266 50025266 AGTTGGCGCTGCGGGCCGGGCGGGGGCCGCGGAAGCTGCGATGCGGACAGGGCAGCGGCGGTGAC AGTTGGCGCTGCGGGCCGGGCGGGGGCCGCGGGAGCTGCGATGCGGACAGGGCAGCGGCGGTGAC A G CNEP1R1 Ensembl:ENSG00000205423 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:50025217..50025402 26863196 MeRIP-seq:(Medium) rs1223217803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4371470,Human_RBP_ID_18419477,Human_RBP_ID_18986279 Human_Splice_Rec_1710653,Human_Splice_Rec_1710665,Human_Splice_Rec_1710675,Human_Splice_Rec_1710685,Human_Splice_Rec_1710687,Human_Splice_Rec_1710695,Human_Splice_Rec_1710701,Human_Splice_Rec_1710707,Human_Splice_Rec_1710717 95172 RMVar_ID_95172 Human_SNP_ID_602267361 m1A Human chr16 + 50025287 50025287 50025287 GGGGGCCGCGGAAGCTGCGATGCGGACAGGGCAGCGGCGGTGACCCGAGCTGCCGCCCGACATGA GGGGGCCGCGGAAGCTGCGATGCGGACAGGGCCGCGGCGGTGACCCGAGCTGCCGCCCGACATGA A C CNEP1R1 Ensembl:ENSG00000205423 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:50025239..50025448;chr16:50025238..50025412 26863196 MeRIP-seq:(Medium) rs965740497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393081,Human_RBP_ID_18419477,Human_RBP_ID_18986279 Human_Splice_Rec_1710653,Human_Splice_Rec_1710665,Human_Splice_Rec_1710675,Human_Splice_Rec_1710685,Human_Splice_Rec_1710687,Human_Splice_Rec_1710695,Human_Splice_Rec_1710701,Human_Splice_Rec_1710707,Human_Splice_Rec_1710717 RMVar_hsa_circ_112468,RMVar_hsa_circ_178280 95173 RMVar_ID_95173 Human_SNP_ID_602267362 m1A Human chr16 + 50025287 50025287 50025287 GGGGGCCGCGGAAGCTGCGATGCGGACAGGGCAGCGGCGGTGACCCGAGCTGCCGCCCGACATGA GGGGGCCGCGGAAGCTGCGATGCGGACAGGGCGGCGGCGGTGACCCGAGCTGCCGCCCGACATGA A G CNEP1R1 Ensembl:ENSG00000205423 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:50025239..50025448;chr16:50025238..50025412 26863196 MeRIP-seq:(Medium) rs965740497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393081,Human_RBP_ID_18419477,Human_RBP_ID_18986279 Human_Splice_Rec_1710653,Human_Splice_Rec_1710665,Human_Splice_Rec_1710675,Human_Splice_Rec_1710685,Human_Splice_Rec_1710687,Human_Splice_Rec_1710695,Human_Splice_Rec_1710701,Human_Splice_Rec_1710707,Human_Splice_Rec_1710717 RMVar_hsa_circ_112468,RMVar_hsa_circ_178280 95174 RMVar_ID_95174 Human_SNP_ID_602277774 m1A Human chr16 + 50066222 50066222 50066222 GTCAGGCCGAGGCGGCTGCGGCGGCGAATGGGACCGGAGGCGAGGAGGACGACGGGCCGGCGGCG GTCAGGCCGAGGCGGCTGCGGCGGCGAATGGGCCCGGAGGCGAGGAGGACGACGGGCCGGCGGCG A C HEATR3 Ensembl:ENSG00000155393 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50066174..50066245 26863196 MeRIP-seq:(Medium) rs1357485855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889720,Human_RBP_ID_18986280 Human_Splice_Rec_1710751,Human_Splice_Rec_1710779,Human_Splice_Rec_1710785 95175 RMVar_ID_95175 Human_SNP_ID_602277782 m1A Human chr16 + 50066238 50066238 50066238 TGCGGCGGCGAATGGGACCGGAGGCGAGGAGGACGACGGGCCGGCGGCGGAGCTGCTGGAAAAGG TGCGGCGGCGAATGGGACCGGAGGCGAGGAGGTCGACGGGCCGGCGGCGGAGCTGCTGGAAAAGG A T HEATR3 Ensembl:ENSG00000155393 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:50066188..50066353 26863196 MeRIP-seq:(Medium) rs755328786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889720,Human_RBP_ID_4371496,Human_RBP_ID_18986280,Human_RBP_ID_19071558 Human_Splice_Rec_1710751,Human_Splice_Rec_1710779,Human_Splice_Rec_1710785 95176 RMVar_ID_95176 Human_SNP_ID_602278218 m1A Human chr16 + 50067441 50067441 50067441 AGAGAGCCAGGAGGCATGGGAAAATAGGGGGAAGAATATTCCCCACAAAGGGAGCAGCAACAGCA AGAGAGCCAGGAGGCATGGGAAAATAGGGGGAGGAATATTCCCCACAAAGGGAGCAGCAACAGCA A G HEATR3 Ensembl:ENSG00000155393 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:50067390..50067595 26863196 MeRIP-seq:(Medium) rs897862349 Functional Loss SNV dbSNP153 33..33 33 - - - 95177 RMVar_ID_95177 Human_SNP_ID_602300464 m1A Human chr16 + 50153315 50153286 50153315 CGCTGCCGCCGCCGCCGCTCGCTCTTCTGTGGAGCCGCCGCCGCCGCCGCCGCCATTTGCACGGG CGCT_____________________________GCCGCCGCCGCCGCCGCCGCCATTTGCACGGG TGCCGCCGCCGCCGCTCGCTCTTCTGTGGA T TENT4B Ensembl:ENSG00000121274 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50153267..50153804 26863196 MeRIP-seq:(Medium) rs1412944419 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_4393082,Human_RBP_ID_9325113 95178 RMVar_ID_95178 Human_SNP_ID_602300500 m1A Human chr16 + 50153315 50153315 50153315 CGCTGCCGCCGCCGCCGCTCGCTCTTCTGTGGAGCCGCCGCCGCCGCCGCCGCCATTTGCACGGG CGCTGCCGCCGCCGCCGCTCGCTCTTCTGTGGGGCCGCCGCCGCCGCCGCCGCCATTTGCACGGG A G TENT4B Ensembl:ENSG00000121274 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50153267..50153804 26863196 MeRIP-seq:(Medium) rs1249936863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393082,Human_RBP_ID_9325113 95179 RMVar_ID_95179 Human_SNP_ID_602300846 m1A Human chr16 - 50154000 50154000 50154000 CGAGGACGCCGAGGGAGGCGAGGACGCCGAGGAGCCCGCCCGGCGGGCCCAGGCCCCGGGCTGGT CGAGGACGCCGAGGGAGGCGAGGACGCCGAGGTGCCCGCCCGGCGGGCCCAGGCCCCGGGCTGGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:50153951..50154259 26863196 MeRIP-seq:(Medium) rs1270696531 Functional Loss SNV dbSNP153 33..33 33 - - - 95180 RMVar_ID_95180 Human_SNP_ID_602300847 m1A Human chr16 - 50154000 50154000 50154000 CGAGGACGCCGAGGGAGGCGAGGACGCCGAGGAGCCCGCCCGGCGGGCCCAGGCCCCGGGCTGGT CGAGGACGCCGAGGGAGGCGAGGACGCCGAGGCGCCCGCCCGGCGGGCCCAGGCCCCGGGCTGGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:50153951..50154259 26863196 MeRIP-seq:(Medium) rs1270696531 Functional Loss SNV dbSNP153 33..33 33 - - - 95181 RMVar_ID_95181 Human_SNP_ID_602300870 m1A Human chr16 + 50154040 50154040 50154040 GTCCTCGCCTCCCTCGGCGTCCTCGTCCCCGCACCCTTCGGCCGCCGTCCCCGCCGCCGATCCAG GTCCTCGCCTCCCTCGGCGTCCTCGTCCCCGCCCCCTTCGGCCGCCGTCCCCGCCGCCGATCCAG A C TENT4B Ensembl:ENSG00000121274 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50153989..50154199 26863196 MeRIP-seq:(Medium) rs879227372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_893602 RMVar_hsa_circ_79929,RMVar_hsa_circ_178299 95182 RMVar_ID_95182 Human_SNP_ID_602323242 m1A Human chr16 - 50245719 50245719 50245719 CCCCCTGCAGGAGCGCCCGTGTTTCTGGAAGGATCCACAGACGGCGGGCCAGTGCCCTCCTCCCA CCCCCTGCAGGAGCGCCCGTGTTTCTGGAAGGCTCCACAGACGGCGGGCCAGTGCCCTCCTCCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50245716..50245904 26863196 MeRIP-seq:(Medium) rs1322438124 Functional Loss SNV dbSNP153 33..33 33 - - - 95183 RMVar_ID_95183 Human_SNP_ID_602323401 m1A Human chr16 - 50246205 50246205 50246205 CCGCCCGCCGCGCTCCCCCGCGCCCCGCGCTCACCTGCTGCGCGCTCCCGCTCCACCGCCGCCCG CCGCCCGCCGCGCTCCCCCGCGCCCCGCGCTCGCCTGCTGCGCGCTCCCGCTCCACCGCCGCCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:50246181..50246374;chr16:50246175..50246522 26863196 MeRIP-seq:(Medium) rs1377588633 Functional Loss SNV dbSNP153 33..33 33 - - - 95184 RMVar_ID_95184 Human_SNP_ID_602323689 m1A Human chr16 - 50247225 50247225 50247225 CTCCCCACAGCCTGTCCCCAGCTCCACAGCCCACAAACTCCCTTCTACAAGGGCACCTGCCCACG CTCCCCACAGCCTGTCCCCAGCTCCACAGCCCCCAAACTCCCTTCTACAAGGGCACCTGCCCACG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:50247175..50247314 26863196 MeRIP-seq:(Medium) rs1433184068 Functional Loss SNV dbSNP153 33..33 33 - - - 95185 RMVar_ID_95185 Human_SNP_ID_602340007 m1A Human chr16 - 50310206 50310206 50310206 TCCCAGTTCTCCCCACTCCCTCTCCAGGAGACAACCCACCCAAAACCCCACTGCTCCCAACACAC TCCCAGTTCTCCCCACTCCCTCTCCAGGAGACGACCCACCCAAAACCCCACTGCTCCCAACACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:50310156..50310264 26863196 MeRIP-seq:(Medium) rs1472451687 Functional Loss SNV dbSNP153 33..33 33 - - - 95186 RMVar_ID_95186 Human_SNP_ID_602355723 m1A Human chr16 - 50368227 50368227 50368227 GAGGGAACGAAGTCACCGAACTCTCCACGGGCAGCTCGGGGCACGACTCCAGCCTCTTCGAAGAC GAGGGAACGAAGTCACCGAACTCTCCACGGGCGGCTCGGGGCACGACTCCAGCCTCTTCGAAGAC T C BRD7 Ensembl:ENSG00000166164 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:50368176..50368300 26863196 MeRIP-seq:(Medium) rs762078120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4371742,Human_RBP_ID_6518129,Human_RBP_ID_8808186,Human_RBP_ID_9286295,Human_RBP_ID_26330097,Human_RBP_ID_26810340 Human_Splice_Rec_1711252,Human_Splice_Rec_1711284,Human_Splice_Rec_1711326,Human_Splice_Rec_1711336 RMVar_hsa_circ_178324,RMVar_hsa_circ_85881 95187 RMVar_ID_95187 Human_SNP_ID_602356012 m1A Human chr16 + 50368773 50368773 50368773 TGTCCGACTTGTGCTTCTTGTGCTTCTTGCCCATGTCCGACCGGGCCCCGGTGCCCGCCCCCCGC TGTCCGACTTGTGCTTCTTGTGCTTCTTGCCCCTGTCCGACCGGGCCCCGGTGCCCGCCCCCCGC A C AC007493.2 Ensembl:ENSG00000261393 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:50368156..50368784 26863410 MeRIP-seq:(Medium) rs776671264 Functional Loss SNV dbSNP153 33..33 33 - - - 95188 RMVar_ID_95188 Human_SNP_ID_602356013 m1A Human chr16 + 50368773 50368773 50368773 TGTCCGACTTGTGCTTCTTGTGCTTCTTGCCCATGTCCGACCGGGCCCCGGTGCCCGCCCCCCGC TGTCCGACTTGTGCTTCTTGTGCTTCTTGCCCGTGTCCGACCGGGCCCCGGTGCCCGCCCCCCGC A G AC007493.2 Ensembl:ENSG00000261393 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:50368156..50368784 26863410 MeRIP-seq:(Medium) rs776671264 Functional Loss SNV dbSNP153 33..33 33 - - - 95189 RMVar_ID_95189 Human_SNP_ID_602551852 m1A Human chr16 + 51151290 51151290 51151290 GCTGGGGCAGAATAAAAAATTACTAAAAAAAAATCTTCTCAAAATTACGGAAATCGAGCGGCGGC GCTGGGGCAGAATAAAAAATTACTAAAAAAAACTCTTCTCAAAATTACGGAAATCGAGCGGCGGC A C AC087564.1 Ensembl:ENSG00000285367 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:51151201..51151375 26863410 MeRIP-seq:(Medium) rs781336249 Functional Loss SNV dbSNP153 33..33 33 - - - 95190 RMVar_ID_95190 Human_SNP_ID_602551853 m1A Human chr16 + 51151290 51151290 51151290 GCTGGGGCAGAATAAAAAATTACTAAAAAAAAATCTTCTCAAAATTACGGAAATCGAGCGGCGGC GCTGGGGCAGAATAAAAAATTACTAAAAAAAAGTCTTCTCAAAATTACGGAAATCGAGCGGCGGC A G AC087564.1 Ensembl:ENSG00000285367 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:51151201..51151375 26863410 MeRIP-seq:(Medium) rs781336249 Functional Loss SNV dbSNP153 33..33 33 - - - 95191 RMVar_ID_95191 Human_SNP_ID_602680665 m1A Human chr16 + 51646731 51646731 51646731 ATACTTTGCAAAACCACGAAACCAAGGTGGCTATGGCGGTTCCAGCAGCAGCAGTAGCTATGGCA ATACTTTGCAAAACCACGAAACCAAGGTGGCTGTGGCGGTTCCAGCAGCAGCAGTAGCTATGGCA A G HNRNPA1P48 Ensembl:ENSG00000224578 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1334145533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475285 95192 RMVar_ID_95192 Human_SNP_ID_602680675 m1A Human chr16 + 51646745 51646745 51646745 CACGAAACCAAGGTGGCTATGGCGGTTCCAGCAGCAGCAGTAGCTATGGCAGTGGCAGAAGATTT CACGAAACCAAGGTGGCTATGGCGGTTCCAGCGGCAGCAGTAGCTATGGCAGTGGCAGAAGATTT A G HNRNPA1P48 Ensembl:ENSG00000224578 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs868364556 Functional Loss SNV dbSNP153 33..33 33 - - - 95193 RMVar_ID_95193 Human_SNP_ID_602680676 m1A Human chr16 + 51646745 51646745 51646745 CACGAAACCAAGGTGGCTATGGCGGTTCCAGCAGCAGCAGTAGCTATGGCAGTGGCAGAAGATTT CACGAAACCAAGGTGGCTATGGCGGTTCCAGCTGCAGCAGTAGCTATGGCAGTGGCAGAAGATTT A T HNRNPA1P48 Ensembl:ENSG00000224578 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs868364556 Functional Loss SNV dbSNP153 33..33 33 - - - 95194 RMVar_ID_95194 Human_SNP_ID_603048477 m1A Human chr16 - 53042255 53042252 53042255 AGGAGAGGGGTGAGGGAAAAGGGGTAGGGAGGAGGGAGGAAGAGAAAAATGGGGAGAGGGTGGGC AGGAGAGGGGTGAGGGAAAAGGGGTAGGGAGG___GAGGAAGAGAAAAATGGGGAGAGGGTGGGC CCCT C AC007906.2 Ensembl:ENSG00000277639 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:53042223..53042300 26863196 MeRIP-seq:(Medium) rs558094399 Functional Loss DEL dbSNP153 33..35 33 - - - 95195 RMVar_ID_95195 Human_SNP_ID_603051047 m1A Human chr16 - 53052946 53052945 53052946 GGAGCAGGAGGAAGAGGAGGAGAAGCAGGAGCAGGGGGAGGAGGAGGAGGCAGAGCAGGAGGAGG GGAGCAGGAGGAAGAGGAGGAGAAGCAGGAGC_GGGGGAGGAGGAGGAGGCAGAGCAGGAGGAGG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:53052900..53053060 26863196 MeRIP-seq:(Medium) rs1337480811 Functional Loss DEL dbSNP153 33..33 33 - - - 95196 RMVar_ID_95196 Human_SNP_ID_603052521 m1A Human chr16 + 53058556 53058556 53058556 TGTACAGAGATAGCCAAGAGCTTGGCAAGGCCAGGGGACTCAAGGAGAGCCAGTGGGCAGGGAGT TGTACAGAGATAGCCAAGAGCTTGGCAAGGCCCGGGGACTCAAGGAGAGCCAGTGGGCAGGGAGT A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:53058508..53058592 26863196 MeRIP-seq:(Medium) rs1329645444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12751099 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 95197 RMVar_ID_95197 Human_SNP_ID_603069816 m1A Human chr16 + 53131123 53131123 53131123 CCGCCTCGGGCGTGGGGAGGAAGCCCGGGGGCACCGCGGGGCAGCGGCCGCTGCTCAACTGGTGG CCGCCTCGGGCGTGGGGAGGAAGCCCGGGGGCGCCGCGGGGCAGCGGCCGCTGCTCAACTGGTGG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:53131058..53131595 26863196 MeRIP-seq:(Medium) rs112757932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3504557,Human_RBP_ID_26779713 GWAS_ID_12478,GWAS_ID_12479,GWAS_ID_12480,GWAS_ID_12481,GWAS_ID_12482,GWAS_ID_12483,GWAS_ID_12484,GWAS_ID_12485,GWAS_ID_12486,GWAS_ID_12487,GWAS_ID_12488,GWAS_ID_12489,GWAS_ID_12490,GWAS_ID_12491,GWAS_ID_12492,GWAS_ID_12493,GWAS_ID_12494,GWAS_ID_12495,GWAS_ID_12496,GWAS_ID_12497,GWAS_ID_12498,GWAS_ID_12499,GWAS_ID_12500,GWAS_ID_12501,GWAS_ID_12502,GWAS_ID_12503,GWAS_ID_12504,GWAS_ID_12505,GWAS_ID_12506,GWAS_ID_12507,GWAS_ID_12508,GWAS_ID_12509,GWAS_ID_12510,GWAS_ID_12511,GWAS_ID_12512,GWAS_ID_12513,GWAS_ID_12514,GWAS_ID_12515,GWAS_ID_12516,GWAS_ID_12517,GWAS_ID_12518,GWAS_ID_12519,GWAS_ID_12520,GWAS_ID_12521,GWAS_ID_12522,GWAS_ID_12523,GWAS_ID_12524,GWAS_ID_12525,GWAS_ID_12526,GWAS_ID_12527,GWAS_ID_12528,GWAS_ID_12529,GWAS_ID_12530,GWAS_ID_12531,GWAS_ID_12532,GWAS_ID_12533,GWAS_ID_12534,GWAS_ID_12535,GWAS_ID_12536,GWAS_ID_12537 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 95198 RMVar_ID_95198 Human_SNP_ID_603069875 m1A Human chr16 + 53131269 53131269 53131269 TCGAGGCGGGGGGCGGCGGGGGCGCCTCAGTCATGGCGAAGCGCGAGAGTCAGCGAGCGGCGGTG TCGAGGCGGGGGGCGGCGGGGGCGCCTCAGTCTTGGCGAAGCGCGAGAGTCAGCGAGCGGCGGTG A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:53131030..53155936 26863196 MeRIP-seq:(Medium) rs915865353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3502718,Human_RBP_ID_8084901,Human_RBP_ID_18482347,Human_RBP_ID_22714371 Human_Splice_Rec_1712899 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 95199 RMVar_ID_95199 Human_SNP_ID_603070117 m1A Human chr16 + 53131811 53131811 53131811 CCCGGAGCACGGGACGTCCCCGGCGCTTTCCCAGGCCTTGCCTCTCGGTTCCGACCGCAGTGCCT CCCGGAGCACGGGACGTCCCCGGCGCTTTCCCGGGCCTTGCCTCTCGGTTCCGACCGCAGTGCCT A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:53131763..53131888 32194978 MeRIP-seq:(Medium) rs1238487372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6518612 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 95200 RMVar_ID_95200 Human_SNP_ID_603070130 m1A Human chr16 + 53131865 53131865 53131865 CCGCAGTGCCTTCCCCGCGATCCTTCACCCCGAGTGCCTCTCCCCGTCTGCAGCGTGGCCCGGAC CCGCAGTGCCTTCCCCGCGATCCTTCACCCCGGGTGCCTCTCCCCGTCTGCAGCGTGGCCCGGAC A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:53131779..53131958 26863196 MeRIP-seq:(Medium) rs752397464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3504564,Human_RBP_ID_5237261,Human_RBP_ID_17371446,Human_RBP_ID_18482350,Human_RBP_ID_22370202,Human_RBP_ID_26779715 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 95201 RMVar_ID_95201 Human_SNP_ID_603158627 m1A Human chr16 + 53500301 53500301 53500301 TCCAAACAAAGAAAGTCAGTGGTGTATCATCCAAATCTTCTGTCTTCGGCATTCACTTTACCTTA TCCAAACAAAGAAAGTCAGTGGTGTATCATCCGAATCTTCTGTCTTCGGCATTCACTTTACCTTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:53500250..53501126 26863196 MeRIP-seq:(Medium) rs1161163070 Functional Loss SNV dbSNP153 33..33 33 - - - 95202 RMVar_ID_95202 Human_SNP_ID_603158628 m1A Human chr16 - 53500306 53500303 53500306 TGTTTTAAGGTAAAGTGAATGCCGAAGACAGAAGATTTGGATGATACACCACTGACTTTCTTTGT TGTTTTAAGGTAAAGTGAATGCCGAAGACAGA___TTTGGATGATACACCACTGACTTTCTTTGT ATCT A AKTIP Ensembl:ENSG00000166971 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:53500255..53500374 26863196 MeRIP-seq:(Medium) rs1258305648 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1843501 Human_Splice_Rec_1713340,Human_Splice_Rec_1713341,Human_Splice_Rec_1713360,Human_Splice_Rec_1713361,Human_Splice_Rec_1713380,Human_Splice_Rec_1713381,Human_Splice_Rec_1713397,Human_Splice_Rec_1713412,Human_Splice_Rec_1713413,Human_Splice_Rec_1713422,Human_Splice_Rec_1713423,Human_Splice_Rec_1713430,Human_Splice_Rec_1713431,Human_Splice_Rec_1713438,Human_Splice_Rec_1713439,Human_Splice_Rec_1713446,Human_Splice_Rec_1713447,Human_Splice_Rec_1713452,Human_Splice_Rec_1713453,Human_Splice_Rec_1713458,Human_Splice_Rec_1713459,Human_Splice_Rec_1713464 RMVar_hsa_circ_321096,RMVar_hsa_circ_66267,RMVar_hsa_circ_287467,RMVar_hsa_circ_178452 95203 RMVar_ID_95203 Human_SNP_ID_603208053 m1A Human chr16 - 53704202 53704202 53704202 CATACCTTAGCTTCGCGCTCTCGTTCCTCGGCAGTCGGGGTGCGCTTCATGCTGCCACTAAAGCC CATACCTTAGCTTCGCGCTCTCGTTCCTCGGCGGTCGGGGTGCGCTTCATGCTGCCACTAAAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:53704151..53704268 26863196 MeRIP-seq:(Medium) rs73609956 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_543 95204 RMVar_ID_95204 Human_SNP_ID_603226072 m1A Human chr16 - 53785477 53785477 53785477 CTTTCTCATCAATTCATTCCCCAAATGGCCCAATCCCTGCCATCCTATCAAAAACAGCACTCTCA CTTTCTCATCAATTCATTCCCCAAATGGCCCAGTCCCTGCCATCCTATCAAAAACAGCACTCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:53785471..53785588 26863196 MeRIP-seq:(Medium) rs780278261 Functional Loss SNV dbSNP153 33..33 33 - - - 95205 RMVar_ID_95205 Human_SNP_ID_603255031 m1A Human chr16 + 53911213 53911213 53911213 GAAAGCACTTAGCACATGGCAGGCATCTCCACAGAGACAGTGGCTGAGCGATTGGAGTGAGTAAG GAAAGCACTTAGCACATGGCAGGCATCTCCACCGAGACAGTGGCTGAGCGATTGGAGTGAGTAAG A C FTO Ensembl:ENSG00000140718 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:53911209..53911458 26863196 MeRIP-seq:(Medium) rs1402714178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340040,RMVar_hsa_circ_343245,RMVar_hsa_circ_178476,RMVar_hsa_circ_178473,RMVar_hsa_circ_104875,RMVar_hsa_circ_178474,RMVar_hsa_circ_101702,RMVar_hsa_circ_271656,RMVar_hsa_circ_178480,RMVar_hsa_circ_178475,RMVar_hsa_circ_280905,RMVar_hsa_circ_178481,RMVar_hsa_circ_362995 95206 RMVar_ID_95206 Human_SNP_ID_603284229 m1A Human chr16 + 54040713 54040713 54040713 CAAACGGTTAAGTGCAAAGTCCCTGAGGCTGGAATGGGCTTAATGTCGTGGAGAAACAGGAAGAG CAAACGGTTAAGTGCAAAGTCCCTGAGGCTGGGATGGGCTTAATGTCGTGGAGAAACAGGAAGAG A G FTO Ensembl:ENSG00000140718 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:54040709..54040792 26863196 MeRIP-seq:(Medium) rs1427217880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104875,RMVar_hsa_circ_178474,RMVar_hsa_circ_101702,RMVar_hsa_circ_178475 95207 RMVar_ID_95207 Human_SNP_ID_603343789 m1A Human chr16 + 54283469 54283469 54283469 AACTCCACCCCCCAAAATCAACCGGACAAACAAACCTCACAGCGAATGCGGGGTGCCACAGAAGC AACTCCACCCCCCAAAATCAACCGGACAAACAGACCTCACAGCGAATGCGGGGTGCCACAGAAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:54283421..54283541 26863196 MeRIP-seq:(Medium) rs562272318 Functional Loss SNV dbSNP153 33..33 33 - - - 95208 RMVar_ID_95208 Human_SNP_ID_603343808 m1A Human chr16 - 54283532 54283529 54283533 AAAACTAAACAAAGAAAGTAAGAAAAAGAAATAAAACCAGTCCTCCTCAGCCCTCCCCAAGTCGC AAAACTAAACAAAGAAAGTAAGAAAAAGAAA____ACCAGTCCTCCTCAGCCCTCCCCAAGTCGC TTTTA T IRX3 Ensembl:ENSG00000177508 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:54283366..54283674 26863196 MeRIP-seq:(Medium) rs1318902253 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_475470,Human_RBP_ID_2491835,Human_RBP_ID_5113524 95209 RMVar_ID_95209 Human_SNP_ID_603343923 m1A Human chr16 - 54283773 54283773 54283773 CGCCCTAGGCAGCCTCTGCGCTCCTGAATCTCACCTCTTTTGCTACTACTGTCTCTCTCTTCCAG CGCCCTAGGCAGCCTCTGCGCTCCTGAATCTCGCCTCTTTTGCTACTACTGTCTCTCTCTTCCAG T C IRX3 Ensembl:ENSG00000177508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:54283733..54283920 26863196 MeRIP-seq:(Medium) rs1023932424 Functional Loss SNV dbSNP153 33..33 33 - - - 95210 RMVar_ID_95210 Human_SNP_ID_603343925 m1A Human chr16 + 54283781 54283781 54283781 GAGAGACAGTAGTAGCAAAAGAGGTGAGATTCAGGAGCGCAGAGGCTGCCTAGGGCGGGGAGATC GAGAGACAGTAGTAGCAAAAGAGGTGAGATTCGGGAGCGCAGAGGCTGCCTAGGGCGGGGAGATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:54283743..54283889 26863196 MeRIP-seq:(Medium) rs775139195 Functional Loss SNV dbSNP153 33..33 33 - - - 95211 RMVar_ID_95211 Human_SNP_ID_603343928 m1A Human chr16 + 54283789 54283789 54283789 GTAGTAGCAAAAGAGGTGAGATTCAGGAGCGCAGAGGCTGCCTAGGGCGGGGAGATCCTACTTGG GTAGTAGCAAAAGAGGTGAGATTCAGGAGCGCTGAGGCTGCCTAGGGCGGGGAGATCCTACTTGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:54283753..54283880 26863196 MeRIP-seq:(Medium) rs1264930226 Functional Loss SNV dbSNP153 33..33 33 - - - 95212 RMVar_ID_95212 Human_SNP_ID_603344254 m1A Human chr16 + 54284601 54284601 54284601 GTCCCAGCAGGTGCGGAGGGGCAGAGCCCAGCAGGGAGAGCGGGTGCAGGCGGGGGCCGGGCGGT GTCCCAGCAGGTGCGGAGGGGCAGAGCCCAGCGGGGAGAGCGGGTGCAGGCGGGGGCCGGGCGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:54284551..54284942 26863196 MeRIP-seq:(Medium) rs1383214418 Functional Loss SNV dbSNP153 33..33 33 - - - 95213 RMVar_ID_95213 Human_SNP_ID_603344625 m1A Human chr16 - 54285228 54285228 54285228 GAGCGAGCGCGAGGAGGAAGACGAAGAGGAGGACGAGGAGGACGGCAAACGCGAGCTAGAGCTGG GAGCGAGCGCGAGGAGGAAGACGAAGAGGAGGGCGAGGAGGACGGCAAACGCGAGCTAGAGCTGG T C IRX3 Ensembl:ENSG00000177508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr16:54285055..54285328;chr16:54284518..54285375;chr16:54285118..54285325 26863196 MeRIP-seq:(Medium) rs1465301616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4372548,Human_RBP_ID_27443337 95214 RMVar_ID_95214 Human_SNP_ID_603345005 m1A Human chr16 + 54285982 54285982 54285982 CCCCGGGCCCCCGCGCTGCCGCCGCTGCCGCCAGCGGCCCCCGGGCGCTCGGACGGGTAAAGCGG CCCCGGGCCCCCGCGCTGCCGCCGCTGCCGCCGGCGGCCCCCGGGCGCTCGGACGGGTAAAGCGG A G AC018553.2 Ensembl:ENSG00000283689 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:54285943..54286064 26863196 MeRIP-seq:(Medium) rs1246359219 Functional Loss SNV dbSNP153 33..33 33 - - - 95215 RMVar_ID_95215 Human_SNP_ID_603510788 m1A Human chr16 - 54931016 54931016 54931016 CCTCGCTGGCTTCCCGCGCGCCTCCGGCTGCGACCGCCGCGCCCGCTCCTCTGCGCGCCTCGCTC CCTCGCTGGCTTCCCGCGCGCCTCCGGCTGCGGCCGCCGCGCCCGCTCCTCTGCGCGCCTCGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:54930742..54932067;chr16:54930648..54931196 26863196 MeRIP-seq:(Medium) rs1452185153 Functional Loss SNV dbSNP153 33..33 33 - - - 95216 RMVar_ID_95216 Human_SNP_ID_603511462 m1A Human chr16 + 54932815 54932815 54932815 TGGACGCCGCGGAACCGCAGCGAGGACGAGGAAGAGGAGGAGAACATTGACCTGGAGAAGAACGA TGGACGCCGCGGAACCGCAGCGAGGACGAGGAGGAGGAGGAGAACATTGACCTGGAGAAGAACGA A G IRX5 Ensembl:ENSG00000176842 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:54932764..54933238 26863196 MeRIP-seq:(Medium) rs150223604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1714219,Human_Splice_Rec_1714231,Human_Splice_Rec_1714233 95217 RMVar_ID_95217 Human_SNP_ID_603511467 m1A Human chr16 + 54932826 54932826 54932826 GAACCGCAGCGAGGACGAGGAAGAGGAGGAGAACATTGACCTGGAGAAGAACGACGAGGACGAGC GAACCGCAGCGAGGACGAGGAAGAGGAGGAGAGCATTGACCTGGAGAAGAACGACGAGGACGAGC A G IRX5 Ensembl:ENSG00000176842 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:54932776..54933169 26863196 MeRIP-seq:(Medium) rs1377397171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1714219,Human_Splice_Rec_1714231,Human_Splice_Rec_1714233 95218 RMVar_ID_95218 Human_SNP_ID_603660468 m1A Human chr16 + 55505702 55505702 55505702 CCACCAACCCTCAGAGCCACCCCTAAAGAGATACTTTGATATTTTCAACGCAGCCCTGCTTTGGG CCACCAACCCTCAGAGCCACCCCTAAAGAGATCCTTTGATATTTTCAACGCAGCCCTGCTTTGGG A C MMP2 Ensembl:ENSG00000087245 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7201 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_miRNA_ID_1646329,Human_miRNA_ID_1651855 Clinvar_Rec_544 GWAS_ID_12538,GWAS_ID_12539,GWAS_ID_12540,GWAS_ID_12541,GWAS_ID_12542,GWAS_ID_12543,GWAS_ID_12544 RMVar_hsa_circ_89298,RMVar_hsa_circ_178492 95219 RMVar_ID_95219 Human_SNP_ID_603661487 m1A Human chr16 + 55509529 55509529 55509529 GAGTCTGAGGAGGGAGGTGGCCTGAAGGGGGCATGGGTCTGAGGAGGGAGGTGGCCCGAGGGGAG GAGTCTGAGGAGGGAGGTGGCCTGAAGGGGGCGTGGGTCTGAGGAGGGAGGTGGCCCGAGGGGAG A G LPCAT2 Ensembl:ENSG00000087253 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:55509429..55509815 26863196 MeRIP-seq:(Medium) rs1275817254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_816585,Human_RBP_ID_8184606,Human_RBP_ID_9419275 95220 RMVar_ID_95220 Human_SNP_ID_603677381 m1A Human chr16 + 55583019 55583019 55583019 GTGCCATGTGTTTTCATTACCAAAAGAAGTCCAGACAACCCCCTCCACCGCCAGTAATAAAGTCA GTGCCATGTGTTTTCATTACCAAAAGAAGTCCTGACAACCCCCTCCACCGCCAGTAATAAAGTCA A T LPCAT2 Ensembl:ENSG00000087253 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:55582971..55583055 26863196 MeRIP-seq:(Medium) rs1054079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_763393 95221 RMVar_ID_95221 Human_SNP_ID_603863903 m1A Human chr16 - 56340796 56340796 56340796 ACAGAGTGGAGGGGTGAGTGAGGGGCGGCAGCATCCAGGGCCCTGACCCACCGCGGCCAATGACA ACAGAGTGGAGGGGTGAGTGAGGGGCGGCAGCGTCCAGGGCCCTGACCCACCGCGGCCAATGACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56340684..56340851 26863196 MeRIP-seq:(Medium) rs1309765813 Functional Loss SNV dbSNP153 33..33 33 - - - 95222 RMVar_ID_95222 Human_SNP_ID_603865133 m1A Human chr16 + 56345096 56345096 56345096 CCAACTCTAAAGGGAGAGTCCTAGGACTCCTTAGAGGAGGCTTCACTGCGGAGATCCCTGAGCAG CCAACTCTAAAGGGAGAGTCCTAGGACTCCTTGGAGGAGGCTTCACTGCGGAGATCCCTGAGCAG A G GNAO1 Ensembl:ENSG00000087258 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:56345046..56345197 32194978 MeRIP-seq:(Medium) rs1206191833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316685 95223 RMVar_ID_95223 Human_SNP_ID_603865393 m1A Human chr16 + 56346072 56346072 56346072 TGGGTGCTCAGCCCTTCCTGCCCTCCATCCCCAGCCTGCCTTTCTCTTCCTTTGGATGCTCCATC TGGGTGCTCAGCCCTTCCTGCCCTCCATCCCCTGCCTGCCTTTCTCTTCCTTTGGATGCTCCATC A T GNAO1 Ensembl:ENSG00000087258 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:56345945..56346146 32194978 MeRIP-seq:(Medium) rs1488809875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316685 95224 RMVar_ID_95224 Human_SNP_ID_603869756 m1A Human chr16 + 56362743 56362742 56362744 GGAAGAGAAATGTCACATAGAAAGTATTACAAAGAAGGATTAAATTTATCAGCTGTCCAAACACT GGAAGAGAAATGTCACATAGAAAGTATTACAA__AAGGATTAAATTTATCAGCTGTCCAAACACT AAG A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:56362692..56362842 32194978 MeRIP-seq:(Medium) rs760303996 Functional Loss DEL dbSNP153 33..34 33 - - - 95225 RMVar_ID_95225 Human_SNP_ID_603869809 m1A Human chr16 - 56362865 56362865 56362865 CTTCCTCAGCTGCCTCCTGCGCCCTGTGCCCGACTGACTGGAGGAGGCCTGTCCCAATTCTGCCC CTTCCTCAGCTGCCTCCTGCGCCCTGTGCCCGCCTGACTGGAGGAGGCCTGTCCCAATTCTGCCC T G AMFR Ensembl:ENSG00000159461 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:56362817..56362975 26863196 MeRIP-seq:(Medium) rs1255853079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475673,Human_RBP_ID_761687,Human_RBP_ID_894443,Human_RBP_ID_8187022,Human_RBP_ID_9325995,Human_RBP_ID_17653037,Human_RBP_ID_18680786,Human_RBP_ID_22441011,Human_RBP_ID_23692902,Human_RBP_ID_24370812,Human_RBP_ID_26441692,Human_RBP_ID_26810347 Human_miRNA_ID_642019 RMVar_hsa_circ_107159,RMVar_hsa_circ_117430,RMVar_hsa_circ_178520,RMVar_hsa_circ_178521 95226 RMVar_ID_95226 Human_SNP_ID_603869842 m1A Human chr16 - 56362925 56362925 56362925 GCTGGCTGCCGCCGCGGAACGGAGGCTTCAGAAGCAGCAGACCTCCTAGCGCTCCCTTGCCTTCC GCTGGCTGCCGCCGCGGAACGGAGGCTTCAGACGCAGCAGACCTCCTAGCGCTCCCTTGCCTTCC T G AMFR Ensembl:ENSG00000159461 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56362876..56363025 26863196 MeRIP-seq:(Medium) rs762776771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107159,RMVar_hsa_circ_117430,RMVar_hsa_circ_178520,RMVar_hsa_circ_178521 95227 RMVar_ID_95227 Human_SNP_ID_603874755 m1A Human chr16 - 56383485 56383485 56383485 TCTGGGTTGCTCTGTGGGCAGTTCTGGACCTCAGTGAGGAGATCAAGTGAGAGATGCACATTTGG TCTGGGTTGCTCTGTGGGCAGTTCTGGACCTCCGTGAGGAGATCAAGTGAGAGATGCACATTTGG T G AMFR Ensembl:ENSG00000159461 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56383476..56383652 26863196 MeRIP-seq:(Medium) rs1456017999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12757564 RMVar_hsa_circ_37204,RMVar_hsa_circ_107159,RMVar_hsa_circ_117430,RMVar_hsa_circ_178520,RMVar_hsa_circ_178521,RMVar_hsa_circ_75167,RMVar_hsa_circ_85419,RMVar_hsa_circ_111419,RMVar_hsa_circ_334718,RMVar_hsa_circ_95377,RMVar_hsa_circ_58383,RMVar_hsa_circ_178522,RMVar_hsa_circ_178524,RMVar_hsa_circ_178525,RMVar_hsa_circ_178523,RMVar_hsa_circ_18847,RMVar_hsa_circ_371388,RMVar_hsa_circ_268266,RMVar_hsa_circ_178529 95228 RMVar_ID_95228 Human_SNP_ID_603874848 m1A Human chr16 + 56384039 56384039 56384039 ATTCCTATCACAGTGTTGTTCCCCTACTTGCCAGGCCCCAACCATAATGACCTTTCTCAGTTCCT ATTCCTATCACAGTGTTGTTCCCCTACTTGCCCGGCCCCAACCATAATGACCTTTCTCAGTTCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56384027..56384209 26863196 MeRIP-seq:(Medium) rs1240370733 Functional Loss SNV dbSNP153 33..33 33 - - - 95229 RMVar_ID_95229 Human_SNP_ID_603881505 m1A Human chr16 - 56409514 56409514 56409514 ATTTTCATCTTTGGTGTGCTGAATGTCCAGACAGTGGAAGAGGTGGTCATGTGGTGCCTCTGGTT ATTTTCATCTTTGGTGTGCTGAATGTCCAGACGGTGGAAGAGGTGGTCATGTGGTGCCTCTGGTT T C AMFR Ensembl:ENSG00000159461 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:56408156..56409569 32194978 MeRIP-seq:(Medium) rs1195578044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475692,Human_RBP_ID_4372995,Human_RBP_ID_5358140,Human_RBP_ID_9285784,Human_RBP_ID_17883829,Human_RBP_ID_23692981,Human_RBP_ID_26945963 Human_Splice_Rec_1715356,Human_Splice_Rec_1715357,Human_Splice_Rec_1715420,Human_Splice_Rec_1715421,Human_Splice_Rec_1715430,Human_Splice_Rec_1715431,Human_Splice_Rec_1715440,Human_Splice_Rec_1715441 Human_miRNA_ID_2969421 RMVar_hsa_circ_117430,RMVar_hsa_circ_178521,RMVar_hsa_circ_334718,RMVar_hsa_circ_178522,RMVar_hsa_circ_293239,RMVar_hsa_circ_327858,RMVar_hsa_circ_16894,RMVar_hsa_circ_178530,RMVar_hsa_circ_178531,RMVar_hsa_circ_178540,RMVar_hsa_circ_93483,RMVar_hsa_circ_282557,RMVar_hsa_circ_109796,RMVar_hsa_circ_58883,RMVar_hsa_circ_178541,RMVar_hsa_circ_376893,RMVar_hsa_circ_285788,RMVar_hsa_circ_178542,RMVar_hsa_circ_178544,RMVar_hsa_circ_272257,RMVar_hsa_circ_178545 95230 RMVar_ID_95230 Human_SNP_ID_603884564 m1A Human chr16 + 56422586 56422579 56422587 GCCTGTGCCTAGCACTGTCCTCCCCACGCCAGACCGAGCTCCACATGCTGGTTTCTCTATCTGGA GCCTGTGCCTAGCACTGTCCTCCCCA________CGAGCTCCACATGCTGGTTTCTCTATCTGGA ACGCCAGAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56422580..56422703 26863196 MeRIP-seq:(Medium) rs1280019401 Functional Loss DEL dbSNP153 27..34 33 - - - 95231 RMVar_ID_95231 Human_SNP_ID_603884569 m1A Human chr16 + 56422586 56422586 56422586 GCCTGTGCCTAGCACTGTCCTCCCCACGCCAGACCGAGCTCCACATGCTGGTTTCTCTATCTGGA GCCTGTGCCTAGCACTGTCCTCCCCACGCCAGGCCGAGCTCCACATGCTGGTTTCTCTATCTGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56422580..56422703 26863196 MeRIP-seq:(Medium) rs1356345615 Functional Loss SNV dbSNP153 33..33 33 - - - 95232 RMVar_ID_95232 Human_SNP_ID_603885325 m1A Human chr16 - 56425436 56425432 56425436 CCGGCCCGGCCCGGCGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGACGCCAGAGCCCGTGGG CCGGCCCGGCCCGGCGCGGCGGCGGCGGCGGC____GCAGCGGCAGCGACGCCAGAGCCCGTGGG CCGCT C AMFR Ensembl:ENSG00000159461 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:56425413..56425495 26863410 MeRIP-seq:(Medium) rs1388647673 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_233914,Human_RBP_ID_817511,Human_RBP_ID_4393109,Human_RBP_ID_9325125 RMVar_hsa_circ_117430,RMVar_hsa_circ_178521 95233 RMVar_ID_95233 Human_SNP_ID_603885326 m1A Human chr16 - 56425436 56425436 56425436 CCGGCCCGGCCCGGCGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGACGCCAGAGCCCGTGGG CCGGCCCGGCCCGGCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGACGCCAGAGCCCGTGGG T C AMFR Ensembl:ENSG00000159461 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:56425413..56425495 26863410 MeRIP-seq:(Medium) rs1352707233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233914,Human_RBP_ID_817511,Human_RBP_ID_4393109,Human_RBP_ID_9325125 RMVar_hsa_circ_117430,RMVar_hsa_circ_178521 95234 RMVar_ID_95234 Human_SNP_ID_603891417 m1A Human chr16 + 56451153 56451153 56451153 TCTGCTGGATGTACTTGTTGCCGAACTGAGTGACCCCCCGGGGCCAGCCGGTCTGCGAGCGATTG TCTGCTGGATGTACTTGTTGCCGAACTGAGTGCCCCCCCGGGGCCAGCCGGTCTGCGAGCGATTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56451114..56451294 26863196 MeRIP-seq:(Medium) rs755431752 Functional Loss SNV dbSNP153 33..33 33 - - - 95235 RMVar_ID_95235 Human_SNP_ID_603891426 m1A Human chr16 - 56451183 56451183 56451183 GGAGCTCGCCAGCATGTCTGTGGTACCGCCCAATCGCTCGCAGACCGGCTGGCCCCGGGGGGTCA GGAGCTCGCCAGCATGTCTGTGGTACCGCCCAGTCGCTCGCAGACCGGCTGGCCCCGGGGGGTCA T C NUDT21 Ensembl:ENSG00000167005 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56451136..56451300 26863196 MeRIP-seq:(Medium) rs1457214228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233987,Human_RBP_ID_818184,Human_RBP_ID_4393844,Human_RBP_ID_5142491,Human_RBP_ID_9325996,Human_RBP_ID_17371454,Human_RBP_ID_17653038,Human_RBP_ID_22442042,Human_RBP_ID_26810361 Human_Splice_Rec_1715447,Human_Splice_Rec_1715479 Human_miRNA_ID_2663053 RMVar_hsa_circ_87420,RMVar_hsa_circ_178547 95236 RMVar_ID_95236 Human_SNP_ID_603891591 m1A Human chr16 - 56451577 56451577 56451577 TTCCCAAGGCACAGAACCACGCCACGCAGATCAAGACGCTACCTTCCTGAGGGTACTGCAACTCC TTCCCAAGGCACAGAACCACGCCACGCAGATCGAGACGCTACCTTCCTGAGGGTACTGCAACTCC T C NUDT21 Ensembl:ENSG00000167005 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:56451526..56451775;chr16:56451526..56453285 26863196 MeRIP-seq:(Medium) rs1195051232 Functional Loss SNV dbSNP153 33..33 33 - - - 95237 RMVar_ID_95237 Human_SNP_ID_603891602 m1A Human chr16 - 56451591 56451591 56451591 TTCCCATTCATCTCTTCCCAAGGCACAGAACCACGCCACGCAGATCAAGACGCTACCTTCCTGAG TTCCCATTCATCTCTTCCCAAGGCACAGAACCTCGCCACGCAGATCAAGACGCTACCTTCCTGAG T A NUDT21 Ensembl:ENSG00000167005 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:56451526..56451702 26863196 MeRIP-seq:(Medium) rs574676974 Functional Loss SNV dbSNP153 33..33 33 - - - 95238 RMVar_ID_95238 Human_SNP_ID_603891603 m1A Human chr16 - 56451591 56451591 56451591 TTCCCATTCATCTCTTCCCAAGGCACAGAACCACGCCACGCAGATCAAGACGCTACCTTCCTGAG TTCCCATTCATCTCTTCCCAAGGCACAGAACCGCGCCACGCAGATCAAGACGCTACCTTCCTGAG T C NUDT21 Ensembl:ENSG00000167005 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:56451526..56451702 26863196 MeRIP-seq:(Medium) rs574676974 Functional Loss SNV dbSNP153 33..33 33 - - - 95239 RMVar_ID_95239 Human_SNP_ID_603898008 m1A Human chr16 + 56477114 56477114 56477114 TTGTGCCACTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAAAAAAAAGAAGA TTGTGCCACTGCACTCCAGCCTGGGCAACAAGGGTGAAACTCTGTCTCAAAAAAAAAAAAGAAGA A G OGFOD1 Ensembl:ENSG00000087263 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112162270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126136 GWAS_ID_12545,GWAS_ID_12546,GWAS_ID_12547,GWAS_ID_12548,GWAS_ID_12549,GWAS_ID_12550,GWAS_ID_12551,GWAS_ID_12552,GWAS_ID_12553,GWAS_ID_12554,GWAS_ID_12555,GWAS_ID_12556,GWAS_ID_12557,GWAS_ID_12558,GWAS_ID_12559,GWAS_ID_12560,GWAS_ID_12561,GWAS_ID_12562,GWAS_ID_12563,GWAS_ID_12564,GWAS_ID_12565,GWAS_ID_12566,GWAS_ID_12567,GWAS_ID_12568,GWAS_ID_12569,GWAS_ID_12570,GWAS_ID_12571,GWAS_ID_12572,GWAS_ID_12573,GWAS_ID_12574,GWAS_ID_12575 RMVar_hsa_circ_178551,RMVar_hsa_circ_98818,RMVar_hsa_circ_114582,RMVar_hsa_circ_112805,RMVar_hsa_circ_110916,RMVar_hsa_circ_178557,RMVar_hsa_circ_178558,RMVar_hsa_circ_178561,RMVar_hsa_circ_105393,RMVar_hsa_circ_104978,RMVar_hsa_circ_178562,RMVar_hsa_circ_178563 95240 RMVar_ID_95240 Human_SNP_ID_603908424 m1A Human chr16 + 56519904 56519902 56519904 GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGACAAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGGCCAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC ACA GCC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56519854..56520009 26863196 MeRIP-seq:(Medium) rs796816065 Functional Loss MNV dbSNP153 31..33 33 - - - 95241 RMVar_ID_95241 Human_SNP_ID_603908426 m1A Human chr16 + 56519904 56519904 56519904 GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGACAAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGACCAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56519854..56520009 26863196 MeRIP-seq:(Medium) rs78076550 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_545,Clinvar_Rec_546 GWAS_ID_12576,GWAS_ID_12577,GWAS_ID_12578,GWAS_ID_12579,GWAS_ID_12580,GWAS_ID_12581,GWAS_ID_12582,GWAS_ID_12583,GWAS_ID_12584,GWAS_ID_12585 95242 RMVar_ID_95242 Human_SNP_ID_603931580 m1A Human chr16 - 56608643 56608643 56608643 CAGGAGCAGTTGGGATCCATGGCGAGCTGAAGAGGCGGCTAGAGTCGGGACAGGTTGCACGCGGG CAGGAGCAGTTGGGATCCATGGCGAGCTGAAGGGGCGGCTAGAGTCGGGACAGGTTGCACGCGGG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:56608576..56608767 26863196 MeRIP-seq:(Medium) rs1257363028 Functional Loss SNV dbSNP153 33..33 33 - - - 95243 RMVar_ID_95243 Human_SNP_ID_603931598 m1A Human chr16 - 56608685 56608685 56608685 CTACAGTCTACACTGGGCATCCCCAGCCTCTTACCGGCGGCGCAGGAGCAGTTGGGATCCATGGC CTACAGTCTACACTGGGCATCCCCAGCCTCTTCCCGGCGGCGCAGGAGCAGTTGGGATCCATGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:56608597..56608712;chr16:56608601..56608898;chr16:56608601..56608748 26863410,32194978,32194978 MeRIP-seq:(Medium) rs757928620 Functional Loss SNV dbSNP153 33..33 33 - - - 95244 RMVar_ID_95244 Human_SNP_ID_603931706 m1A Human chr16 - 56609045 56609045 56609045 AAAGAGAGGATCCCACTTACTTTTCTTGCAGGAGGTGCATTTGCACTCTTTGCATTTGCAGGAGC AAAGAGAGGATCCCACTTACTTTTCTTGCAGGGGGTGCATTTGCACTCTTTGCATTTGCAGGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:56608943..56609103;chr16:56608932..56609115 26863196 MeRIP-seq:(Medium) rs1334688686 Functional Loss SNV dbSNP153 33..33 33 - - - 95245 RMVar_ID_95245 Human_SNP_ID_603931773 m1A Human chr16 + 56609213 56609213 56609213 AGTGATCCTTATCAGGGAGAGCAGGAATCCTTATTCCCGGTGTCGCTAGTACTCATCTCTGCCGC AGTGATCCTTATCAGGGAGAGCAGGAATCCTTGTTCCCGGTGTCGCTAGTACTCATCTCTGCCGC A G MT2A Ensembl:ENSG00000125148 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56609210..56609406 26863196 MeRIP-seq:(Medium) rs775941407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22584269 RMVar_hsa_circ_92058,RMVar_hsa_circ_112190,RMVar_hsa_circ_178577,RMVar_hsa_circ_178578 95246 RMVar_ID_95246 Human_SNP_ID_603936359 m1A Human chr16 - 56625830 56625830 56625830 TTGGGGTCCATTTCGAGCAAAGGGGATGCTGGAGCTCACACCAGTGAGACGAACAAGCAGTCAGG TTGGGGTCCATTTCGAGCAAAGGGGATGCTGGGGCTCACACCAGTGAGACGAACAAGCAGTCAGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:56625761..56626550 26863196 MeRIP-seq:(Medium) rs1488434972 Functional Loss SNV dbSNP153 33..33 33 - - - 95247 RMVar_ID_95247 Human_SNP_ID_603936365 m1A Human chr16 - 56625842 56625842 56625842 GCGCAAGAGCAGTTGGGGTCCATTTCGAGCAAAGGGGATGCTGGAGCTCACACCAGTGAGACGAA GCGCAAGAGCAGTTGGGGTCCATTTCGAGCAATGGGGATGCTGGAGCTCACACCAGTGAGACGAA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr16:56625734..56625982;chr16:56625776..56625974 26863196 MeRIP-seq:(Medium) rs370357493 Functional Loss SNV dbSNP153 33..33 33 - - - 95248 RMVar_ID_95248 Human_SNP_ID_603936731 m1A Human chr16 - 56626832 56626827 56626832 AGAGTGAGAGGTGGCAGTAGACTTGACCGGGCACCTCCCTGCCCTAATAGCAAGCCTGGCTCGAG AGAGTGAGAGGTGGCAGTAGACTTGACCGGGC_____CCTGCCCTAATAGCAAGCCTGGCTCGAG GGAGGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56626831..56626909 26863196 MeRIP-seq:(Medium) rs772119790 Functional Loss DEL dbSNP153 33..37 33 - - - 95249 RMVar_ID_95249 Human_SNP_ID_603952497 m1A Human chr16 - 56682522 56682522 56682522 CAGTTGGGGTCCATTTCGAGGCAAGGAGAAGCAGGAGTTCCCGATCAAGAGGAAAACACGCAGCG CAGTTGGGGTCCATTTCGAGGCAAGGAGAAGCGGGAGTTCCCGATCAAGAGGAAAACACGCAGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56682472..56682670 26863196 MeRIP-seq:(Medium) rs200672898 Functional Loss SNV dbSNP153 33..33 33 - - - 95250 RMVar_ID_95250 Human_SNP_ID_603952501 m1A Human chr16 - 56682532 56682532 56682532 CGAGCAGGAGCAGTTGGGGTCCATTTCGAGGCAAGGAGAAGCAGGAGTTCCCGATCAAGAGGAAA CGAGCAGGAGCAGTTGGGGTCCATTTCGAGGCGAGGAGAAGCAGGAGTTCCCGATCAAGAGGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56682451..56682615 26863196 MeRIP-seq:(Medium) rs1394714302 Functional Loss SNV dbSNP153 33..33 33 - - - 95251 RMVar_ID_95251 Human_SNP_ID_603952995 m1A Human chr16 - 56684069 56684069 56684069 CAGGTTTATATAGGTTGCTCTATTTACATCTGAGAGCACAGCTGTCCTGGCATCAGGCACAGCAG CAGGTTTATATAGGTTGCTCTATTTACATCTGCGAGCACAGCTGTCCTGGCATCAGGCACAGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56684020..56684089 26863196 MeRIP-seq:(Medium) rs756014665 Functional Loss SNV dbSNP153 33..33 33 - - - 95252 RMVar_ID_95252 Human_SNP_ID_603953008 m1A Human chr16 + 56684097 56684097 56684097 GCTCTCAGATGTAAATAGAGCAACCTATATAAACCTGGATTTTTTTTTTTTTTTTTTTTGTACAA GCTCTCAGATGTAAATAGAGCAACCTATATAAGCCTGGATTTTTTTTTTTTTTTTTTTTGTACAA A G AC026461.1,MT1X Ensembl:ENSG00000259827,Ensembl:ENSG00000187193 lincRNA,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56684051..56684100 26863196 MeRIP-seq:(Medium) rs778034731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475889,Human_RBP_ID_6521573,Human_RBP_ID_9063140,Human_RBP_ID_21889290 Human_miRNA_ID_736136 RMVar_hsa_circ_121107,RMVar_hsa_circ_178589 95253 RMVar_ID_95253 Human_SNP_ID_603963742 m1A Human chr16 + 56730174 56730174 56730174 GAGCGGCGCGAGAAGCGGCGGCCGCGTCCTCAAGCCGGCACCTGAGCGGCGGAGACGGCTGTAGC GAGCGGCGCGAGAAGCGGCGGCCGCGTCCTCATGCCGGCACCTGAGCGGCGGAGACGGCTGTAGC A T NUP93 Ensembl:ENSG00000102900 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:56730126..56730267;chr16:56730126..56730284 26863196 MeRIP-seq:(Medium) rs1022190326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126244,Human_RBP_ID_760766,Human_RBP_ID_4393854,Human_RBP_ID_5237262,Human_RBP_ID_5571816,Human_RBP_ID_8812373,Human_RBP_ID_9286300 Human_Splice_Rec_1715949,Human_Splice_Rec_1715963,Human_Splice_Rec_1715973,Human_Splice_Rec_1716015,Human_Splice_Rec_1716059 RMVar_hsa_circ_85420,RMVar_hsa_circ_178590 95254 RMVar_ID_95254 Human_SNP_ID_603963752 m1A Human chr16 + 56730196 56730196 56730196 CGCGTCCTCAAGCCGGCACCTGAGCGGCGGAGACGGCTGTAGCACAAGGTAAGGGTGTGTCTGGT CGCGTCCTCAAGCCGGCACCTGAGCGGCGGAGGCGGCTGTAGCACAAGGTAAGGGTGTGTCTGGT A G NUP93 Ensembl:ENSG00000102900 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56730146..56730262 26863196 MeRIP-seq:(Medium) rs1178080250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126244,Human_RBP_ID_4393854,Human_RBP_ID_5237262,Human_RBP_ID_8812373,Human_RBP_ID_9286300,Human_RBP_ID_19074442 Human_Splice_Rec_1715949,Human_Splice_Rec_1715963,Human_Splice_Rec_1715973,Human_Splice_Rec_1716015,Human_Splice_Rec_1716059 RMVar_hsa_circ_85420,RMVar_hsa_circ_178590 95255 RMVar_ID_95255 Human_SNP_ID_603964558 m1A Human chr16 + 56733453 56733451 56733454 GAGAAGTAGAGCTTGAGATTGGCTGAGTGTTGAGGAGGTGAAAGGGGCGCTGGGGTGACTTGAAG GAGAAGTAGAGCTTGAGATTGGCTGAGTGTT___GAGGTGAAAGGGGCGCTGGGGTGACTTGAAG TGAG T NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56733451..56733628 26863196 MeRIP-seq:(Medium) rs1236383924 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_85420,RMVar_hsa_circ_178590 95256 RMVar_ID_95256 Human_SNP_ID_603968283 m1A Human chr16 + 56748319 56748318 56748320 GAACAGCTTGCTGCTGAGACTGAGGGCATCTCAGAGCTTCCCCATGTGGAACGGAACTTACAGGA GAACAGCTTGCTGCTGAGACTGAGGGCATCTC__AGCTTCCCCATGTGGAACGGAACTTACAGGA CAG C NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56748270..56748378 26863196 MeRIP-seq:(Medium) rs1285784621 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_475891,Human_RBP_ID_1519463,Human_RBP_ID_1843765,Human_RBP_ID_3947687,Human_RBP_ID_4393855,Human_RBP_ID_5358144,Human_RBP_ID_9286301,Human_RBP_ID_18680904,Human_RBP_ID_18983802 Human_Splice_Rec_1715950,Human_Splice_Rec_1715966,Human_Splice_Rec_1715974,Human_Splice_Rec_1716016,Human_Splice_Rec_1716078 RMVar_hsa_circ_25462,RMVar_hsa_circ_85420,RMVar_hsa_circ_22527,RMVar_hsa_circ_178590,RMVar_hsa_circ_321734,RMVar_hsa_circ_349228,RMVar_hsa_circ_178591 95257 RMVar_ID_95257 Human_SNP_ID_603968284 m1A Human chr16 + 56748319 56748319 56748319 GAACAGCTTGCTGCTGAGACTGAGGGCATCTCAGAGCTTCCCCATGTGGAACGGAACTTACAGGA GAACAGCTTGCTGCTGAGACTGAGGGCATCTCCGAGCTTCCCCATGTGGAACGGAACTTACAGGA A C NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56748270..56748378 26863196 MeRIP-seq:(Medium) rs754667340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475891,Human_RBP_ID_1519463,Human_RBP_ID_1843765,Human_RBP_ID_3947687,Human_RBP_ID_4393855,Human_RBP_ID_5358144,Human_RBP_ID_9286301,Human_RBP_ID_18680904,Human_RBP_ID_18983802 Human_Splice_Rec_1715950,Human_Splice_Rec_1715966,Human_Splice_Rec_1715974,Human_Splice_Rec_1716016,Human_Splice_Rec_1716078 RMVar_hsa_circ_25462,RMVar_hsa_circ_85420,RMVar_hsa_circ_22527,RMVar_hsa_circ_178590,RMVar_hsa_circ_321734,RMVar_hsa_circ_349228,RMVar_hsa_circ_178591 95258 RMVar_ID_95258 Human_SNP_ID_603988132 m1A Human chr16 + 56830605 56830605 56830605 TGCATGCGCTGTGGAGACCTGCTTGCCGCTTCACAGGTAGTTAATCGAGCCCAGCACCAGCTGGG TGCATGCGCTGTGGAGACCTGCTTGCCGCTTCTCAGGTAGTTAATCGAGCCCAGCACCAGCTGGG A T NUP93 Ensembl:ENSG00000102900 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:56830555..56831535 32194978 MeRIP-seq:(Medium) rs763589213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44010,Human_RBP_ID_1519467,Human_RBP_ID_8811930,Human_RBP_ID_18983803,Human_RBP_ID_22441024,Human_RBP_ID_22584277,Human_RBP_ID_22759852 Human_Splice_Rec_1715958,Human_Splice_Rec_1715959,Human_Splice_Rec_1715990,Human_Splice_Rec_1715991,Human_Splice_Rec_1716032,Human_Splice_Rec_1716033,Human_Splice_Rec_1716106,Human_Splice_Rec_1716107,Human_Splice_Rec_1716174,Human_Splice_Rec_1716175 Human_miRNA_ID_2473346,Human_miRNA_ID_2473347 RMVar_hsa_circ_178593,RMVar_hsa_circ_103358,RMVar_hsa_circ_77865,RMVar_hsa_circ_178594,RMVar_hsa_circ_18118,RMVar_hsa_circ_127700,RMVar_hsa_circ_92014,RMVar_hsa_circ_178598,RMVar_hsa_circ_178599,RMVar_hsa_circ_178602,RMVar_hsa_circ_5701,RMVar_hsa_circ_178603 95259 RMVar_ID_95259 Human_SNP_ID_603989708 m1A Human chr16 - 56836644 56836644 56836644 CTTTATTTTCTGCCACAGAAGCAACTTTGTTGATAATAGGCTTTGTGTCACTAGTAAACTTATCT CTTTATTTTCTGCCACAGAAGCAACTTTGTTGGTAATAGGCTTTGTGTCACTAGTAAACTTATCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:56834773..56839060 32194978 MeRIP-seq:(Medium) rs759630879 Functional Loss SNV dbSNP153 33..33 33 - - - 95260 RMVar_ID_95260 Human_SNP_ID_603989709 m1A Human chr16 - 56836644 56836644 56836644 CTTTATTTTCTGCCACAGAAGCAACTTTGTTGATAATAGGCTTTGTGTCACTAGTAAACTTATCT CTTTATTTTCTGCCACAGAAGCAACTTTGTTGCTAATAGGCTTTGTGTCACTAGTAAACTTATCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:56834773..56839060 32194978 MeRIP-seq:(Medium) rs759630879 Functional Loss SNV dbSNP153 33..33 33 - - - 95261 RMVar_ID_95261 Human_SNP_ID_603997033 m1A Human chr16 + 56865251 56865248 56865251 TGGACACCCAGGCGACAATGGCAGAACTGCCCACAACAGAGACGCCTGGGGACGCCACTTTGTGC TGGACACCCAGGCGACAATGGCAGAACTGC___CAACAGAGACGCCTGGGGACGCCACTTTGTGC CCCA C SLC12A3 Ensembl:ENSG00000070915 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:56865226..56865250 26863196 MeRIP-seq:(Medium) rs763922717 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_96542,RMVar_hsa_circ_126698,RMVar_hsa_circ_178615,RMVar_hsa_circ_178616 95262 RMVar_ID_95262 Human_SNP_ID_603997046 m1A Human chr16 - 56865265 56865265 56865265 GTGAAGCGCCCGCTGCACAAAGTGGCGTCCCCAGGCGTCTCTGTTGTGGGCAGTTCTGCCATTGT GTGAAGCGCCCGCTGCACAAAGTGGCGTCCCCGGGCGTCTCTGTTGTGGGCAGTTCTGCCATTGT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:56865201..56865375 26863196 MeRIP-seq:(Medium) rs1401034070 Functional Loss SNV dbSNP153 33..33 33 - - - 95263 RMVar_ID_95263 Human_SNP_ID_603997076 m1A Human chr16 + 56865317 56865317 56865317 GCGGGCGCTTCACCATCAGCACACTGCTGAGCAGTGATGAGCCCTCTCCACCAGCTGCCTATGAC GCGGGCGCTTCACCATCAGCACACTGCTGAGCGGTGATGAGCCCTCTCCACCAGCTGCCTATGAC A G SLC12A3 Ensembl:ENSG00000070915 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56865266..56865354 26863196 MeRIP-seq:(Medium) rs1470397391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96542,RMVar_hsa_circ_126698,RMVar_hsa_circ_178615,RMVar_hsa_circ_178616 95264 RMVar_ID_95264 Human_SNP_ID_604002136 m1A Human chr16 - 56882434 56882434 56882434 GCTGAAGTTGATGAGGGCATAGGAGCAGAGGAAGAAGTTGGAAATGATGGGGGCTATGGTGTTGA GCTGAAGTTGATGAGGGCATAGGAGCAGAGGAGGAAGTTGGAAATGATGGGGGCTATGGTGTTGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:56882401..56882475 26863196 MeRIP-seq:(Medium) rs748650798 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_547 GWAS_ID_12586 95265 RMVar_ID_95265 Human_SNP_ID_604002621 m1A Human chr16 - 56884103 56884103 56884103 AGGTGAGGAGGAACATGATGACCACGGAGATGATAGCCCCAAACAGCGCCGCCCACTTGTTGTAG AGGTGAGGAGGAACATGATGACCACGGAGATGGTAGCCCCAAACAGCGCCGCCCACTTGTTGTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56884047..56884143 26863196 MeRIP-seq:(Medium) rs1169812154 Functional Loss SNV dbSNP153 33..33 33 - - - 95266 RMVar_ID_95266 Human_SNP_ID_604005127 m1A Human chr16 - 56892193 56892193 56892193 AAGTGGCCCACCCCTAGCCACCCCACAGGGCTAGAGTGCCCTGAGCTCTGAGTGGGAACACTGAC AAGTGGCCCACCCCTAGCCACCCCACAGGGCTTGAGTGCCCTGAGCTCTGAGTGGGAACACTGAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56892178..56892288 26863196 MeRIP-seq:(Medium) rs1200642166 Functional Loss SNV dbSNP153 33..33 33 - - - 95267 RMVar_ID_95267 Human_SNP_ID_604011119 m1A Human chr16 + 56914812 56914812 56914812 TGTCAGGAATGAAGATGTGGAGAGGGGTGTAGAGATGGCAAGGTTGGCAAGGAACAGATAGGCAG TGTCAGGAATGAAGATGTGGAGAGGGGTGTAGCGATGGCAAGGTTGGCAAGGAACAGATAGGCAG A C SLC12A3 Ensembl:ENSG00000070915 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:56914624..56914875 26863196 MeRIP-seq:(Medium) rs1270963405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127714,RMVar_hsa_circ_178621 95268 RMVar_ID_95268 Human_SNP_ID_604011282 m1A Human chr16 + 56915635 56915635 56915635 ATCCATCAGGGAATGCTGGCCTTTCTAGAGCCACGTAGAAAACAATTTTCTGGTTCTTCAAACCT ATCCATCAGGGAATGCTGGCCTTTCTAGAGCCGCGTAGAAAACAATTTTCTGGTTCTTCAAACCT A G SLC12A3 Ensembl:ENSG00000070915 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56915584..56915680 26863196 MeRIP-seq:(Medium) rs1333842348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127714,RMVar_hsa_circ_178621 95269 RMVar_ID_95269 Human_SNP_ID_604015730 m1A Human chr16 + 56932186 56932186 56932186 TGAACTGTCGTTGCAGAGATTGCGGGCGGCTGAGACGCCGCCTGCCTGGCACCTAGGAGCGCAGC TGAACTGTCGTTGCAGAGATTGCGGGCGGCTGGGACGCCGCCTGCCTGGCACCTAGGAGCGCAGC A G HERPUD1 Ensembl:ENSG00000051108 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:56932151..56932300 26863196 MeRIP-seq:(Medium) rs547581145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128100,Human_RBP_ID_816464,Human_RBP_ID_1519483,Human_RBP_ID_4373426,Human_RBP_ID_9063160,Human_RBP_ID_22441028,Human_RBP_ID_22944448 95270 RMVar_ID_95270 Human_SNP_ID_604015736 m1A Human chr16 - 56932196 56932196 56932196 TCGGGGCTCCGCTGCGCTCCTAGGTGCCAGGCAGGCGGCGTCTCAGCCGCCCGCAATCTCTGCAA TCGGGGCTCCGCTGCGCTCCTAGGTGCCAGGCGGGCGGCGTCTCAGCCGCCCGCAATCTCTGCAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:56932146..56932350;chr16:56932126..56932350;chr16:56932143..56932325 26863196 MeRIP-seq:(Medium) rs759433854 Functional Loss SNV dbSNP153 33..33 33 - - - 95271 RMVar_ID_95271 Human_SNP_ID_604015775 m1A Human chr16 + 56932261 56932261 56932261 CACCGCCGCCGCCGCCATGGAGTCCGAGACCGAACCCGAGCCCGTCACGCTCCTGGTGAAGAGCC CACCGCCGCCGCCGCCATGGAGTCCGAGACCGGACCCGAGCCCGTCACGCTCCTGGTGAAGAGCC A G HERPUD1 Ensembl:ENSG00000051108 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:56932165..56932299 26863196 MeRIP-seq:(Medium) rs1367278942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128100,Human_RBP_ID_234567,Human_RBP_ID_763311,Human_RBP_ID_816464,Human_RBP_ID_4393113,Human_RBP_ID_12760082,Human_RBP_ID_22441521,Human_RBP_ID_22944448 95272 RMVar_ID_95272 Human_SNP_ID_604030852 m1A Human chr16 + 56989593 56989593 56989593 TCGTGCAGAGCGCGGAGGAGCCGCGAGCGCTGAGGGTGAGTGCCGGGAGCTCTGAGGGTGAGTGC TCGTGCAGAGCGCGGAGGAGCCGCGAGCGCTGCGGGTGAGTGCCGGGAGCTCTGAGGGTGAGTGC A C NLRC5 Ensembl:ENSG00000140853 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56989576..56989684 26863196 MeRIP-seq:(Medium) rs1191132490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1716683,Human_Splice_Rec_1716731,Human_Splice_Rec_1716827,Human_Splice_Rec_1716829,Human_Splice_Rec_1716833 95273 RMVar_ID_95273 Human_SNP_ID_604031451 m1A Human chr16 - 56991953 56991953 56991953 GGTCCTATTGGATTCAAGGCCCATCCTACTCCAGTATGACCTCATCTTCACCAGTTATATCTGCA GGTCCTATTGGATTCAAGGCCCATCCTACTCCTGTATGACCTCATCTTCACCAGTTATATCTGCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56991945..56992064 26863196 MeRIP-seq:(Medium) rs1482563756 Functional Loss SNV dbSNP153 33..33 33 - - - 95274 RMVar_ID_95274 Human_SNP_ID_604052511 m1A Human chr16 - 57071457 57071457 57071457 CTCACTCACCCCCTTCCCCATTAACCACCAACACCACTCACTCACAACCCTTCCCCATTAACCAC CTCACTCACCCCCTTCCCCATTAACCACCAACGCCACTCACTCACAACCCTTCCCCATTAACCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57071389..57071500 26863196 MeRIP-seq:(Medium) rs1273939470 Functional Loss SNV dbSNP153 33..33 33 - - - 95275 RMVar_ID_95275 Human_SNP_ID_604052512 m1A Human chr16 - 57071457 57071457 57071457 CTCACTCACCCCCTTCCCCATTAACCACCAACACCACTCACTCACAACCCTTCCCCATTAACCAC CTCACTCACCCCCTTCCCCATTAACCACCAACCCCACTCACTCACAACCCTTCCCCATTAACCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57071389..57071500 26863196 MeRIP-seq:(Medium) rs1273939470 Functional Loss SNV dbSNP153 33..33 33 - - - 95276 RMVar_ID_95276 Human_SNP_ID_604060907 m1A Human chr16 + 57104888 57104884 57104889 TAAGGCCCTGAGGCAGGAGAGAGCCTGACAGCAAAGGGAGGCCAGTGCAGCTGGGCCAAAGGAAG TAAGGCCCTGAGGCAGGAGAGAGCCTGAC_____AGGGAGGCCAGTGCAGCTGGGCCAAAGGAAG CAGCAA C CPNE2 Ensembl:ENSG00000140848 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57104883..57104980 26863196 MeRIP-seq:(Medium) rs1384271997 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_269766 95277 RMVar_ID_95277 Human_SNP_ID_604066951 m1A Human chr16 - 57129070 57129070 57129070 TCTGCCCTGAAGGCTCCCCCTGCCCCACTGCCACCTCTAGTCACTCTGCTACTTCCCTTTCCCCT TCTGCCCTGAAGGCTCCCCCTGCCCCACTGCCGCCTCTAGTCACTCTGCTACTTCCCTTTCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57129067..57129143 26863196 MeRIP-seq:(Medium) rs931120162 Functional Loss SNV dbSNP153 33..33 33 - - - 95278 RMVar_ID_95278 Human_SNP_ID_604068801 m1A Human chr16 - 57137199 57137199 57137199 GACGATGGGGGAGAAATTGGTAGGACCGTAGAAGCGGATGTGGGGCAGGCAAGCTGAGTACGCCT GACGATGGGGGAGAAATTGGTAGGACCGTAGAGGCGGATGTGGGGCAGGCAAGCTGAGTACGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57137137..57137223 26863196 MeRIP-seq:(Medium) rs377640626 Functional Loss SNV dbSNP153 33..33 33 - - - 95279 RMVar_ID_95279 Human_SNP_ID_604068802 m1A Human chr16 - 57137199 57137199 57137199 GACGATGGGGGAGAAATTGGTAGGACCGTAGAAGCGGATGTGGGGCAGGCAAGCTGAGTACGCCT GACGATGGGGGAGAAATTGGTAGGACCGTAGACGCGGATGTGGGGCAGGCAAGCTGAGTACGCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57137137..57137223 26863196 MeRIP-seq:(Medium) rs377640626 Functional Loss SNV dbSNP153 33..33 33 - - - 95280 RMVar_ID_95280 Human_SNP_ID_604069943 m1A Human chr16 - 57142293 57142293 57142293 CCTCCAAGTTTCAGCTCACATGTCACTTTCCCAAAAAGCCTTTCCTGAGCCCTCCATCTGGGTCG CCTCCAAGTTTCAGCTCACATGTCACTTTCCCCAAAAGCCTTTCCTGAGCCCTCCATCTGGGTCG T G AC009090.4 Ensembl:ENSG00000279019 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57142287..57142398 26863196 MeRIP-seq:(Medium) rs1368238498 Functional Loss SNV dbSNP153 33..33 33 - - - 95281 RMVar_ID_95281 Human_SNP_ID_604071243 m1A Human chr16 + 57147671 57147669 57147672 CCAACTCGGAGCCCGCCTGAGCTCCAGTGCCCAGCAGCAGCATGTCAGCTGAGCCTCCTGCCCTC CCAACTCGGAGCCCGCCTGAGCTCCAGTGCC___CAGCAGCATGTCAGCTGAGCCTCCTGCCCTC CCAG C CPNE2 Ensembl:ENSG00000140848 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57147622..57147784 26863196 MeRIP-seq:(Medium) rs763464977 Functional Loss DEL dbSNP153 32..34 33 - - - 95282 RMVar_ID_95282 Human_SNP_ID_604071249 m1A Human chr16 - 57147681 57147681 57147681 GTTCCTGGGGGAGGGCAGGAGGCTCAGCTGACATGCTGCTGCTGGGCACTGGAGCTCAGGCGGGC GTTCCTGGGGGAGGGCAGGAGGCTCAGCTGACGTGCTGCTGCTGGGCACTGGAGCTCAGGCGGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:57147631..57147835 26863196 MeRIP-seq:(Medium) rs769131866 Functional Loss SNV dbSNP153 33..33 33 - - - 95283 RMVar_ID_95283 Human_SNP_ID_604072662 m1A Human chr16 - 57154256 57154256 57154256 TTCTCCGTCCCTACACAGGGAGCTCCTCCCCAAGGGTAGATCGGACCGTTCATGCTGCCTATAGG TTCTCCGTCCCTACACAGGGAGCTCCTCCCCAGGGGTAGATCGGACCGTTCATGCTGCCTATAGG T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57154064..57154264 32194978 MeRIP-seq:(Medium) rs766329136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475980,Human_RBP_ID_1282521,Human_RBP_ID_6522090,Human_RBP_ID_9372861,Human_RBP_ID_12760665,Human_RBP_ID_17254664,Human_RBP_ID_26946074 Human_miRNA_ID_2367834,Human_miRNA_ID_3015618,Human_miRNA_ID_3096566 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_75903,RMVar_hsa_circ_178677 95284 RMVar_ID_95284 Human_SNP_ID_604072720 m1A Human chr16 - 57154376 57154376 57154376 GTGCCTACTCTGGGAGCAGCGACTCCGAGTCCAGCTCAGACAGCGAAGGCACCATCAATGCCACC GTGCCTACTCTGGGAGCAGCGACTCCGAGTCCGGCTCAGACAGCGAAGGCACCATCAATGCCACC T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57154326..57167184 32194978 MeRIP-seq:(Medium) rs1223060883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234140,Human_RBP_ID_817409,Human_RBP_ID_9372862,Human_RBP_ID_18163003,Human_RBP_ID_18680974,Human_RBP_ID_26328160 Human_miRNA_ID_2542414,Human_miRNA_ID_2544282,Human_miRNA_ID_2546127,Human_miRNA_ID_2547987,Human_miRNA_ID_2549850,Human_miRNA_ID_2551720,Human_miRNA_ID_2557132,Human_miRNA_ID_2559016,Human_miRNA_ID_2589431 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_75903,RMVar_hsa_circ_178677 95285 RMVar_ID_95285 Human_SNP_ID_604079983 m1A Human chr16 + 57185801 57185801 57185801 GGAAGCTGGAACCCAGGTGTCGCCGCCAGGCCAGGACCGAGGCCGCACTCACCTACCGGCGCGCG GGAAGCTGGAACCCAGGTGTCGCCGCCAGGCCGGGACCGAGGCCGCACTCACCTACCGGCGCGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57185799..57186026 26863196 MeRIP-seq:(Medium) rs1035214425 Functional Loss SNV dbSNP153 33..33 33 - - - 95286 RMVar_ID_95286 Human_SNP_ID_604079986 m1A Human chr16 + 57185823 57185823 57185823 CCGCCAGGCCAGGACCGAGGCCGCACTCACCTACCGGCGCGCGGGAGGCGAGACGACCTCACCTC CCGCCAGGCCAGGACCGAGGCCGCACTCACCTCCCGGCGCGCGGGAGGCGAGACGACCTCACCTC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57185815..57185916 32194978 MeRIP-seq:(Medium) rs1184093842 Functional Loss SNV dbSNP153 33..33 33 - - - 95287 RMVar_ID_95287 Human_SNP_ID_604079987 m1A Human chr16 + 57185823 57185823 57185823 CCGCCAGGCCAGGACCGAGGCCGCACTCACCTACCGGCGCGCGGGAGGCGAGACGACCTCACCTC CCGCCAGGCCAGGACCGAGGCCGCACTCACCTGCCGGCGCGCGGGAGGCGAGACGACCTCACCTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57185815..57185916 32194978 MeRIP-seq:(Medium) rs1184093842 Functional Loss SNV dbSNP153 33..33 33 - - - 95288 RMVar_ID_95288 Human_SNP_ID_604080011 m1A Human chr16 - 57185896 57185896 57185896 TTTCTTCCTTTCATTTTTTTTTCTTTTTTAAGAGCGAGCGGCTCTGCGGTGGCGGTTTGGGGTGG TTTCTTCCTTTCATTTTTTTTTCTTTTTTAAGTGCGAGCGGCTCTGCGGTGGCGGTTTGGGGTGG T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57185865..57186048 26863196 MeRIP-seq:(Medium) rs1021218442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1366028,Human_RBP_ID_6522350,Human_RBP_ID_12761341,Human_RBP_ID_24558671 Human_Splice_Rec_1717731,Human_Splice_Rec_1717767,Human_Splice_Rec_1717787,Human_Splice_Rec_1717797,Human_Splice_Rec_1717825,Human_Splice_Rec_1717839,Human_Splice_Rec_1717853,Human_Splice_Rec_1717861,Human_Splice_Rec_1717875,Human_Splice_Rec_1717883 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 95289 RMVar_ID_95289 Human_SNP_ID_604080016 m1A Human chr16 + 57185907 57185906 57185907 CGCCACCGCAGAGCCGCTCGCTCTTAAAAAAGAAAAAAAAATGAAAGGAAGAAAGAAAGAAACAG CGCCACCGCAGAGCCGCTCGCTCTTAAAAAAG_AAAAAAAATGAAAGGAAGAAAGAAAGAAACAG GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57185905..57186034 26863196 MeRIP-seq:(Medium) rs11383644 Functional Loss DEL dbSNP153 33..33 33 - - - 95290 RMVar_ID_95290 Human_SNP_ID_604080289 m1A Human chr16 + 57186543 57186543 57186543 TCTGAGGGTTGGGGACGTCTGTGAGGGAGGGGAACAGCCGCTCGAGCCTGGGGCGGGCGGACCGG TCTGAGGGTTGGGGACGTCTGTGAGGGAGGGGTACAGCCGCTCGAGCCTGGGGCGGGCGGACCGG A T RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57186334..57186647 26863196 MeRIP-seq:(Medium) rs1200685326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_261501,Human_RBP_ID_3502721,Human_RBP_ID_4393117,Human_RBP_ID_5360390,Human_RBP_ID_9419278,Human_RBP_ID_22415489,Human_RBP_ID_26779255 95291 RMVar_ID_95291 Human_SNP_ID_604094751 m1A Human chr16 - 57245404 57245402 57245404 AAGTCGCCTGCGCCCTGGAGGAGCTACTCACAAAGACAGCGCAAAGCTCTCTCCTTCTAAGGCGT AAGTCGCCTGCGCCCTGGAGGAGCTACTCACA__GACAGCGCAAAGCTCTCTCCTTCTAAGGCGT CTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57245391..57246139 32194978 MeRIP-seq:(Medium) rs754087233 Functional Loss DEL dbSNP153 33..34 33 - - - 95292 RMVar_ID_95292 Human_SNP_ID_604104382 m1A Human chr16 + 57284452 57284452 57284452 TGAGCGCCCCGAGGCGGGAGCGCACGAAGCCCAGGTCCGGGCGCAGCGCCGACACCGAGGCTTCG TGAGCGCCCCGAGGCGGGAGCGCACGAAGCCCGGGTCCGGGCGCAGCGCCGACACCGAGGCTTCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57284402..57284529 26863196 MeRIP-seq:(Medium) rs1429764926 Functional Loss SNV dbSNP153 33..33 33 - - - 95293 RMVar_ID_95293 Human_SNP_ID_604108601 m1A Human chr16 + 57300018 57300018 57300018 AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGAATCCCACTTCTGACAAGCGCTCTTTTCCGGTA AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGGATCCCACTTCTGACAAGCGCTCTTTTCCGGTA A G tRNA-Leu-CAG-2-1 RNACentral:URS00000FB60D tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs192959558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269795,Human_RBP_ID_476100,Human_RBP_ID_1519635,Human_RBP_ID_1843904,Human_RBP_ID_3496844,Human_RBP_ID_5180773,Human_RBP_ID_5274692,Human_RBP_ID_5495841,Human_RBP_ID_6522587,Human_RBP_ID_8435589,Human_RBP_ID_8808476,Human_RBP_ID_9830552,Human_RBP_ID_12762003,Human_RBP_ID_18681030,Human_RBP_ID_20170613,Human_RBP_ID_22203100,Human_RBP_ID_22801747,Human_RBP_ID_22940316,Human_RBP_ID_23128447,Human_RBP_ID_23693615,Human_RBP_ID_26441932,Human_RBP_ID_26946123,Human_RBP_ID_27243127,Human_RBP_ID_27560253 95294 RMVar_ID_95294 Human_SNP_ID_604108630 m1A Human chr16 - 57300039 57300039 57300039 TCGAAGATTTCTCTTCTGAAATACCGGAAAAGAGCGCTTGTCAGAAGTGGGATTCGAACCCACGC TCGAAGATTTCTCTTCTGAAATACCGGAAAAGGGCGCTTGTCAGAAGTGGGATTCGAACCCACGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57299976..57300050 26863196 MeRIP-seq:(Medium) rs572081623 Functional Loss SNV dbSNP153 33..33 33 - - - 95295 RMVar_ID_95295 Human_SNP_ID_604108631 m1A Human chr16 - 57300039 57300039 57300039 TCGAAGATTTCTCTTCTGAAATACCGGAAAAGAGCGCTTGTCAGAAGTGGGATTCGAACCCACGC TCGAAGATTTCTCTTCTGAAATACCGGAAAAGCGCGCTTGTCAGAAGTGGGATTCGAACCCACGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57299976..57300050 26863196 MeRIP-seq:(Medium) rs572081623 Functional Loss SNV dbSNP153 33..33 33 - - - 95296 RMVar_ID_95296 Human_SNP_ID_604108669 m1A Human chr16 + 57300079 57300079 57300079 GGTATTTCAGAAGAGAAATCTTCGACGACCGCACACCAAGAGAGGCCCTCAAACACAGAGGACCG GGTATTTCAGAAGAGAAATCTTCGACGACCGCTCACCAAGAGAGGCCCTCAAACACAGAGGACCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57300031..57300234 26863196 MeRIP-seq:(Medium) rs1326585520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1519636,Human_RBP_ID_1843904,Human_RBP_ID_18681032,Human_RBP_ID_22940317,Human_RBP_ID_25216865,Human_RBP_ID_26946125 95297 RMVar_ID_95297 Human_SNP_ID_604108986 m1A Human chr16 - 57300495 57300484 57300496 AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTCGAATCCCACTTCTGACAGAGCTCAATTACTTTTC AGGTCGCAGTCTCCCCTGGAGGCGTGGGTTC____________TGACAGAGCTCAATTACTTTTC AGAAGTGGGATTC A tRNA-Leu-CAG-2-1 RNACentral:URS00000FB60D tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1373503700 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_476104,Human_RBP_ID_1282542,Human_RBP_ID_1366035,Human_RBP_ID_1519639,Human_RBP_ID_1843907,Human_RBP_ID_2478284,Human_RBP_ID_3496846,Human_RBP_ID_5440682,Human_RBP_ID_5465261,Human_RBP_ID_6522591,Human_RBP_ID_8435594,Human_RBP_ID_9843055,Human_RBP_ID_12762005,Human_RBP_ID_18207451,Human_RBP_ID_18681038,Human_RBP_ID_20170616,Human_RBP_ID_22050810,Human_RBP_ID_22803011,Human_RBP_ID_23128456,Human_RBP_ID_23693626,Human_RBP_ID_24477463,Human_RBP_ID_26946129,Human_RBP_ID_27443471 95298 RMVar_ID_95298 Human_SNP_ID_604145459 m1A Human chr16 - 57439285 57439285 57439285 AGCTTTGACATTATTTTGTCAGGTTTAGTCCCAGGAAGCACCACTCTGCACAGTGCTGAGATTTT AGCTTTGACATTATTTTGTCAGGTTTAGTCCCGGGAAGCACCACTCTGCACAGTGCTGAGATTTT T C CIAPIN1 Ensembl:ENSG00000005194 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57439144..57439385 26863196 MeRIP-seq:(Medium) rs11557673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1843919,Human_RBP_ID_6522619,Human_RBP_ID_12762145,Human_RBP_ID_22442081,Human_RBP_ID_22654270 Human_Splice_Rec_1718096,Human_Splice_Rec_1718112,Human_Splice_Rec_1718128,Human_Splice_Rec_1718129,Human_Splice_Rec_1718140,Human_Splice_Rec_1718154,Human_Splice_Rec_1718166,Human_Splice_Rec_1718176,Human_Splice_Rec_1718198,Human_Splice_Rec_1718210,Human_Splice_Rec_1718222,Human_Splice_Rec_1718234,Human_Splice_Rec_1718242 RMVar_hsa_circ_296748,RMVar_hsa_circ_6729,RMVar_hsa_circ_14846,RMVar_hsa_circ_24891 95299 RMVar_ID_95299 Human_SNP_ID_604147523 m1A Human chr16 + 57447551 57447551 57447551 CGGTATCTGGTGCGCTTGGCCGGGCGGGCTGGAGGCTCCTGCAGCTGCGATGCCTGCCCGGTGAG CGGTATCTGGTGCGCTTGGCCGGGCGGGCTGGTGGCTCCTGCAGCTGCGATGCCTGCCCGGTGAG A T COQ9 Ensembl:ENSG00000088682 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57447501..57447701 26863196 MeRIP-seq:(Medium) rs1226931534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393131,Human_RBP_ID_5495845,Human_RBP_ID_9325138,Human_RBP_ID_17878532 Human_Splice_Rec_1718245,Human_Splice_Rec_1718249,Human_Splice_Rec_1718257,Human_Splice_Rec_1718273,Human_Splice_Rec_1718279,Human_Splice_Rec_1718287,Human_Splice_Rec_1718301,Human_Splice_Rec_1718313,Human_Splice_Rec_1718327,Human_Splice_Rec_1718337,Human_Splice_Rec_1718345 RMVar_hsa_circ_178706,RMVar_hsa_circ_82461 95300 RMVar_ID_95300 Human_SNP_ID_604148440 m1A Human chr16 + 57451118 57451118 57451118 AGCTGTGGGGCTAAGGTCTTCAGATGAGCAGAAGCAGCAGCCTCCCAACTCATTTTCTCAGCAGC AGCTGTGGGGCTAAGGTCTTCAGATGAGCAGAGGCAGCAGCCTCCCAACTCATTTTCTCAGCAGC A G COQ9 Ensembl:ENSG00000088682 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57451068..57452859 32194978 MeRIP-seq:(Medium) rs1336095241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393866,Human_RBP_ID_9374357 Human_Splice_Rec_1718246,Human_Splice_Rec_1718247,Human_Splice_Rec_1718250,Human_Splice_Rec_1718251,Human_Splice_Rec_1718258,Human_Splice_Rec_1718259,Human_Splice_Rec_1718274,Human_Splice_Rec_1718275,Human_Splice_Rec_1718280,Human_Splice_Rec_1718281,Human_Splice_Rec_1718288,Human_Splice_Rec_1718289,Human_Splice_Rec_1718302,Human_Splice_Rec_1718303,Human_Splice_Rec_1718314,Human_Splice_Rec_1718315,Human_Splice_Rec_1718328,Human_Splice_Rec_1718329,Human_Splice_Rec_1718338,Human_Splice_Rec_1718339,Human_Splice_Rec_1718346,Human_Splice_Rec_1718347,Human_Splice_Rec_1718350,Human_Splice_Rec_1718351,Human_Splice_Rec_1718359,Human_Splice_Rec_1718361 RMVar_hsa_circ_178706,RMVar_hsa_circ_82461,RMVar_hsa_circ_358207,RMVar_hsa_circ_367298,RMVar_hsa_circ_27492 95301 RMVar_ID_95301 Human_SNP_ID_604148473 m1A Human chr16 - 57451179 57451179 57451179 TACCTGGGGGGTGAATGAGAAGACTCTGGATCAGGTTTTTCTGCCCCCTGTGTCTCAGAATGCTG TACCTGGGGGGTGAATGAGAAGACTCTGGATCCGGTTTTTCTGCCCCCTGTGTCTCAGAATGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57450999..57451242 26863196 MeRIP-seq:(Medium) rs773595935 Functional Loss SNV dbSNP153 33..33 33 - - - 95302 RMVar_ID_95302 Human_SNP_ID_604148911 m1A Human chr16 + 57452876 57452876 57452876 GAGGAGCAGTTGCAGCACCGCATCCTGACGGCAGCCCTTGAGTTTGTGCCCGCCCACGGGTGGAC GAGGAGCAGTTGCAGCACCGCATCCTGACGGCCGCCCTTGAGTTTGTGCCCGCCCACGGGTGGAC A C COQ9 Ensembl:ENSG00000088682 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57452826..57452985 26863196 MeRIP-seq:(Medium) rs567112416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888774,Human_RBP_ID_18983819,Human_RBP_ID_26330128 Human_Splice_Rec_1718248,Human_Splice_Rec_1718252,Human_Splice_Rec_1718253,Human_Splice_Rec_1718260,Human_Splice_Rec_1718261,Human_Splice_Rec_1718276,Human_Splice_Rec_1718277,Human_Splice_Rec_1718282,Human_Splice_Rec_1718283,Human_Splice_Rec_1718290,Human_Splice_Rec_1718291,Human_Splice_Rec_1718304,Human_Splice_Rec_1718305,Human_Splice_Rec_1718316,Human_Splice_Rec_1718317,Human_Splice_Rec_1718330,Human_Splice_Rec_1718331,Human_Splice_Rec_1718340,Human_Splice_Rec_1718341,Human_Splice_Rec_1718348,Human_Splice_Rec_1718352,Human_Splice_Rec_1718353,Human_Splice_Rec_1718360,Human_Splice_Rec_1718362,Human_Splice_Rec_1718363 RMVar_hsa_circ_7322,RMVar_hsa_circ_178706,RMVar_hsa_circ_82461,RMVar_hsa_circ_358207,RMVar_hsa_circ_367298,RMVar_hsa_circ_27492 95303 RMVar_ID_95303 Human_SNP_ID_604148912 m1A Human chr16 + 57452876 57452876 57452876 GAGGAGCAGTTGCAGCACCGCATCCTGACGGCAGCCCTTGAGTTTGTGCCCGCCCACGGGTGGAC GAGGAGCAGTTGCAGCACCGCATCCTGACGGCGGCCCTTGAGTTTGTGCCCGCCCACGGGTGGAC A G COQ9 Ensembl:ENSG00000088682 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57452826..57452985 26863196 MeRIP-seq:(Medium) rs567112416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888774,Human_RBP_ID_18983819,Human_RBP_ID_26330128 Human_Splice_Rec_1718248,Human_Splice_Rec_1718252,Human_Splice_Rec_1718253,Human_Splice_Rec_1718260,Human_Splice_Rec_1718261,Human_Splice_Rec_1718276,Human_Splice_Rec_1718277,Human_Splice_Rec_1718282,Human_Splice_Rec_1718283,Human_Splice_Rec_1718290,Human_Splice_Rec_1718291,Human_Splice_Rec_1718304,Human_Splice_Rec_1718305,Human_Splice_Rec_1718316,Human_Splice_Rec_1718317,Human_Splice_Rec_1718330,Human_Splice_Rec_1718331,Human_Splice_Rec_1718340,Human_Splice_Rec_1718341,Human_Splice_Rec_1718348,Human_Splice_Rec_1718352,Human_Splice_Rec_1718353,Human_Splice_Rec_1718360,Human_Splice_Rec_1718362,Human_Splice_Rec_1718363 RMVar_hsa_circ_7322,RMVar_hsa_circ_178706,RMVar_hsa_circ_82461,RMVar_hsa_circ_358207,RMVar_hsa_circ_367298,RMVar_hsa_circ_27492 95304 RMVar_ID_95304 Human_SNP_ID_604153830 m1A Human chr16 - 57471861 57471861 57471861 TAATTAACTGCTTTGTGCATGTTCCTATCTGGAGACAGTGCTGAGGGGTTAGGGCCAGAGCCTTC TAATTAACTGCTTTGTGCATGTTCCTATCTGGTGACAGTGCTGAGGGGTTAGGGCCAGAGCCTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57471810..57471960 32194978 MeRIP-seq:(Medium) rs1223288548 Functional Loss SNV dbSNP153 33..33 33 - - - 95305 RMVar_ID_95305 Human_SNP_ID_604153894 m1A Human chr16 - 57472136 57472133 57472136 GCTAGGGAGGTGGTGCAGTCAGCCTCGCTCTCAACGTGACCCGGGGAATGACCACCCAGAGGGAT GCTAGGGAGGTGGTGCAGTCAGCCTCGCTCTC___GTGACCCGGGGAATGACCACCCAGAGGGAT CGTT C DOK4 Ensembl:ENSG00000125170 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57472021..57472171 32194978 MeRIP-seq:(Medium) rs1183830792 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_476195 RMVar_hsa_circ_88035,RMVar_hsa_circ_178718,RMVar_hsa_circ_178717 95306 RMVar_ID_95306 Human_SNP_ID_604154312 m1A Human chr16 + 57473466 57473466 57473466 CAGGATGAATCTGTTGAGGAGGTCTGTTTCCGAGCTGGCCTGGGCTGCCCCATACCCCTCACCTG CAGGATGAATCTGTTGAGGAGGTCTGTTTCCGGGCTGGCCTGGGCTGCCCCATACCCCTCACCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57473417..57473518 32194978 MeRIP-seq:(Medium) rs769963864 Functional Loss SNV dbSNP153 33..33 33 - - - 95307 RMVar_ID_95307 Human_SNP_ID_604156120 m1A Human chr16 - 57479538 57479538 57479538 GGCACCTGGGCATCCTTCCCCTCGCCTCTGCCAGGCCCCGCGCCCCTAAAAGGTGGGAAAACCAT GGCACCTGGGCATCCTTCCCCTCGCCTCTGCCGGGCCCCGCGCCCCTAAAAGGTGGGAAAACCAT T C DOK4 Ensembl:ENSG00000125170 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:57479443..57479593 32194978 MeRIP-seq:(Medium) rs376338750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393135 Human_Splice_Rec_1718449,Human_Splice_Rec_1718463,Human_Splice_Rec_1718477,Human_Splice_Rec_1718493,Human_Splice_Rec_1718503,Human_Splice_Rec_1718509,Human_Splice_Rec_1718521,Human_Splice_Rec_1718529,Human_Splice_Rec_1718537,Human_Splice_Rec_1718545,Human_Splice_Rec_1718553,Human_Splice_Rec_1718561,Human_Splice_Rec_1718569,Human_Splice_Rec_1718577,Human_Splice_Rec_1718587,Human_Splice_Rec_1718593,Human_Splice_Rec_1718599 RMVar_hsa_circ_377433,RMVar_hsa_circ_178719,RMVar_hsa_circ_48424 95308 RMVar_ID_95308 Human_SNP_ID_604156122 m1A Human chr16 + 57479544 57479544 57479544 TTCCCACCTTTTAGGGGCGCGGGGCCTGGCAGAGGCGAGGGGAAGGATGCCCAGGTGCCTGGGTC TTCCCACCTTTTAGGGGCGCGGGGCCTGGCAGTGGCGAGGGGAAGGATGCCCAGGTGCCTGGGTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57479496..57479754 26863196 MeRIP-seq:(Medium) rs1237055537 Functional Loss SNV dbSNP153 33..33 33 - - - 95309 RMVar_ID_95309 Human_SNP_ID_604156294 m1A Human chr16 - 57480272 57480265 57480273 AGAGAAACAGGTAGAGGACCGGGTGGGGCAGGAGGGTAGAGGGGTTTGTGGGGGCTGCTGAGCTG AGAGAAACAGGTAGAGGACCGGGTGGGGCAG________AGGGGTTTGTGGGGGCTGCTGAGCTG TCTACCCTC T DOK4 Ensembl:ENSG00000125170 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57480268..57480360 26863196 MeRIP-seq:(Medium) rs1209731396 Functional Loss DEL dbSNP153 32..39 33 - - - 95310 RMVar_ID_95310 Human_SNP_ID_604157861 m1A Human chr16 + 57486428 57486428 57486428 AGGGCGGCGGCGGCGCCGGGCTCCAGGCGGGGACGGCGAGGGAGGCGCGGCCGCAGGGCTAGGGA AGGGCGGCGGCGGCGCCGGGCTCCAGGCGGGGGCGGCGAGGGAGGCGCGGCCGCAGGGCTAGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:57486263..57486471;chr16:57486245..57486465 26863196 MeRIP-seq:(Medium) rs1279940406 Functional Loss SNV dbSNP153 33..33 33 - - - 95311 RMVar_ID_95311 Human_SNP_ID_604164431 m1A Human chr16 + 57512815 57512815 57512815 ACTGGTTCCATCCTCGGCCTCCTCGGTGCCAAAGCGAGCACTGCGGATCTTCCCGAAGAGGGGAG ACTGGTTCCATCCTCGGCCTCCTCGGTGCCAAGGCGAGCACTGCGGATCTTCCCGAAGAGGGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57512766..57512906 26863196 MeRIP-seq:(Medium) rs778693391 Functional Loss SNV dbSNP153 33..33 33 - - - 95312 RMVar_ID_95312 Human_SNP_ID_604191710 m1A Human chr16 + 57620135 57620135 57620135 CACAGGCCGGTGAGGGACCTGCCCAGACCTGGAGGTAAGAGACGGGTGGGGGACAGGGGTGGGAA CACAGGCCGGTGAGGGACCTGCCCAGACCTGGGGGTAAGAGACGGGTGGGGGACAGGGGTGGGAA A G ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57620085..57620249 26863196 MeRIP-seq:(Medium) rs1555528458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1718779,Human_Splice_Rec_1718805,Human_Splice_Rec_1718829,Human_Splice_Rec_1718833,Human_Splice_Rec_1718837,Human_Splice_Rec_1718839,Human_Splice_Rec_1718847,Human_Splice_Rec_1718873,Human_Splice_Rec_1718877,Human_Splice_Rec_1718881 95313 RMVar_ID_95313 Human_SNP_ID_604193846 m1A Human chr16 - 57628819 57628819 57628819 ACTCACACTATTCCCCTTCCCACCTGCTGTCCAGCCCTTGTTTGGGTACCTGCTGCCAGGTGGAG ACTCACACTATTCCCCTTCCCACCTGCTGTCCTGCCCTTGTTTGGGTACCTGCTGCCAGGTGGAG T A AC018552.3 Ensembl:ENSG00000261633 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57628817..57629124 26863196 MeRIP-seq:(Medium) rs1413066022 Functional Loss SNV dbSNP153 33..33 33 - - - 95314 RMVar_ID_95314 Human_SNP_ID_604193851 m1A Human chr16 + 57628885 57628842 57628886 TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA __________________________________AGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TAGTGTGAGTGTGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAG T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:57628757..57629301;chr16:57628755..57629309 26863196 MeRIP-seq:(Medium) rs1407279304 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_5181315 RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95315 RMVar_ID_95315 Human_SNP_ID_604193893 m1A Human chr16 + 57628885 57628875 57628885 TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGAGAGTGTGAGTGTGTGAGCGT__________GAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGAGTGTGTGA T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:57628757..57629301;chr16:57628755..57629309 26863196 MeRIP-seq:(Medium) rs1356065650 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5181315 RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95316 RMVar_ID_95316 Human_SNP_ID_604193903 m1A Human chr16 + 57628885 57628881 57628885 TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGAGAGTGTGAGTGTGTGAGCGTGAGTGT____GAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGTGA T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:57628757..57629301;chr16:57628755..57629309 26863196 MeRIP-seq:(Medium) rs1236943515 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5181315 RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95317 RMVar_ID_95317 Human_SNP_ID_604193905 m1A Human chr16 + 57628885 57628883 57628885 TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGT__GAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGA T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:57628757..57629301;chr16:57628755..57629309 26863196 MeRIP-seq:(Medium) rs72102673 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5181315 RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95318 RMVar_ID_95318 Human_SNP_ID_604193907 m1A Human chr16 + 57628885 57628885 57628885 TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGAGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA TGAGAGTGTGAGTGTGTGAGCGTGAGTGTGTGTGAGTGTGAGTGTGTGAGTGTGAGTGTGTGAGA A T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr16:57628757..57629301;chr16:57628755..57629309 26863196 MeRIP-seq:(Medium) rs796405169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5181315 RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95319 RMVar_ID_95319 Human_SNP_ID_604194197 m1A Human chr16 + 57629001 57628997 57629001 AGTGTGTGAGAGTGAGTGAGAATGTGAGTGTGAGTGTGAGAGTGTGACTGAGCGTTTGAGTGTGA AGTGTGTGAGAGTGAGTGAGAATGTGAGT____GTGTGAGAGTGTGACTGAGCGTTTGAGTGTGA TGTGA T ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57628786..57629318 26863196 MeRIP-seq:(Medium) rs1420141864 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95320 RMVar_ID_95320 Human_SNP_ID_604194764 m1A Human chr16 + 57630636 57630636 57630636 CACTGGGCAAGGGCCAGTCAGCCTGGTGTGACACTTCCTTTTGTCAGGGATACAAACAAACAAAC CACTGGGCAAGGGCCAGTCAGCCTGGTGTGACGCTTCCTTTTGTCAGGGATACAAACAAACAAAC A G ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57630631..57630795 26863196 MeRIP-seq:(Medium) rs1346181687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95321 RMVar_ID_95321 Human_SNP_ID_604196273 m1A Human chr16 + 57636805 57636805 57636805 TAGGTACTGGAGATGCAGGTGGTGAGCAAGACAGGTGAGACAGCAAAGCTGAGCAAGGGATAACA TAGGTACTGGAGATGCAGGTGGTGAGCAAGACCGGTGAGACAGCAAAGCTGAGCAAGGGATAACA A C ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57636800..57637115 26863196 MeRIP-seq:(Medium) rs956656265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95322 RMVar_ID_95322 Human_SNP_ID_604196274 m1A Human chr16 + 57636805 57636805 57636805 TAGGTACTGGAGATGCAGGTGGTGAGCAAGACAGGTGAGACAGCAAAGCTGAGCAAGGGATAACA TAGGTACTGGAGATGCAGGTGGTGAGCAAGACGGGTGAGACAGCAAAGCTGAGCAAGGGATAACA A G ADGRG1 Ensembl:ENSG00000205336 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57636800..57637115 26863196 MeRIP-seq:(Medium) rs956656265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94149,RMVar_hsa_circ_178722 95323 RMVar_ID_95323 Human_SNP_ID_604200429 m1A Human chr16 + 57651601 57651601 57651601 GCCCTCAGAACATCAGCCTGCCCAGTGCCGCCAGCTTCACCTTCTCCTTCCACAGTAAGGCAACT GCCCTCAGAACATCAGCCTGCCCAGTGCCGCCGGCTTCACCTTCTCCTTCCACAGTAAGGCAACT A G ADGRG1 Ensembl:ENSG00000205336 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:57651551..57651625 26863196 MeRIP-seq:(Medium) rs774670158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27443523 Human_Splice_Rec_1718745,Human_Splice_Rec_1718757,Human_Splice_Rec_1718783,Human_Splice_Rec_1718807,Human_Splice_Rec_1718843,Human_Splice_Rec_1718851,Human_Splice_Rec_1718897,Human_Splice_Rec_1718925,Human_Splice_Rec_1718953,Human_Splice_Rec_1718977,Human_Splice_Rec_1718983,Human_Splice_Rec_1719009,Human_Splice_Rec_1719015,Human_Splice_Rec_1719025,Human_Splice_Rec_1719051,Human_Splice_Rec_1719093,Human_Splice_Rec_1719149,Human_Splice_Rec_1719191,Human_Splice_Rec_1719215,Human_Splice_Rec_1719233,Human_Splice_Rec_1719243 Human_miRNA_ID_115528,Human_miRNA_ID_1277009,Human_miRNA_ID_2621640 RMVar_hsa_circ_29774,RMVar_hsa_circ_178723,RMVar_hsa_circ_9858,RMVar_hsa_circ_372122 95324 RMVar_ID_95324 Human_SNP_ID_604200432 m1A Human chr16 - 57651613 57651611 57651614 CCTCCGCCTGGAAGTTGCCTTACTGTGGAAGGAGAAGGTGAAGCTGGCGGCACTGGGCAGGCTGA CCTCCGCCTGGAAGTTGCCTTACTGTGGAAG___AAGGTGAAGCTGGCGGCACTGGGCAGGCTGA TCTC T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:57651401..57651675 26863196 MeRIP-seq:(Medium) rs755315705 Functional Loss DEL dbSNP153 32..34 33 - - - 95325 RMVar_ID_95325 Human_SNP_ID_604200433 m1A Human chr16 - 57651613 57651613 57651613 CCTCCGCCTGGAAGTTGCCTTACTGTGGAAGGAGAAGGTGAAGCTGGCGGCACTGGGCAGGCTGA CCTCCGCCTGGAAGTTGCCTTACTGTGGAAGGTGAAGGTGAAGCTGGCGGCACTGGGCAGGCTGA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:57651401..57651675 26863196 MeRIP-seq:(Medium) rs1355781777 Functional Loss SNV dbSNP153 33..33 33 - - - 95326 RMVar_ID_95326 Human_SNP_ID_604201101 m1A Human chr16 + 57653996 57653996 57653996 ACCGCTTTCTCCTCCCTGCCAGGCAGTTGCAGAGCCTGGAGTCGAAACTGACCTCTGTGAGATTC ACCGCTTTCTCCTCCCTGCCAGGCAGTTGCAGGGCCTGGAGTCGAAACTGACCTCTGTGAGATTC A G ADGRG1 Ensembl:ENSG00000205336 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57653976..57654100 26863196 MeRIP-seq:(Medium) rs757807546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1718748,Human_Splice_Rec_1718760,Human_Splice_Rec_1718786,Human_Splice_Rec_1718810,Human_Splice_Rec_1718846,Human_Splice_Rec_1718854,Human_Splice_Rec_1718928,Human_Splice_Rec_1718956,Human_Splice_Rec_1718986,Human_Splice_Rec_1719028,Human_Splice_Rec_1719054,Human_Splice_Rec_1719096,Human_Splice_Rec_1719152,Human_Splice_Rec_1719194,Human_Splice_Rec_1719258,Human_Splice_Rec_1719260 RMVar_hsa_circ_29774,RMVar_hsa_circ_178723,RMVar_hsa_circ_9858,RMVar_hsa_circ_372122 95327 RMVar_ID_95327 Human_SNP_ID_604202256 m1A Human chr16 - 57657443 57657443 57657443 CGGCAATGGTGACAAGGCAGGCCAGGGCAGAGACGACACAGCCCACGTAGGAGAGGAGGCTCAGG CGGCAATGGTGACAAGGCAGGCCAGGGCAGAGGCGACACAGCCCACGTAGGAGAGGAGGCTCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57657393..57657546 26863196 MeRIP-seq:(Medium) rs1470700508 Functional Loss SNV dbSNP153 33..33 33 - - - 95328 RMVar_ID_95328 Human_SNP_ID_604223378 m1A Human chr16 + 57735842 57735842 57735842 GGTCGCGCCTGGAGCGGAGCCTCGGCCTCCGGAGCCGCAGCTGCAGGTGGAGTGGGCAAGGGGAC GGTCGCGCCTGGAGCGGAGCCTCGGCCTCCGGTGCCGCAGCTGCAGGTGGAGTGGGCAAGGGGAC A T KATNB1 Ensembl:ENSG00000140854 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57735794..57736070 26863196 MeRIP-seq:(Medium) rs1319541688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4393141,Human_RBP_ID_18418742,Human_RBP_ID_18986373 Human_Splice_Rec_1719521,Human_Splice_Rec_1719537,Human_Splice_Rec_1719573 95329 RMVar_ID_95329 Human_SNP_ID_604223453 m1A Human chr16 + 57736191 57736191 57736191 GAGACCCCGCGAGCATATGGGAAAGGGCAGTAACGGGAGTCTGGCGAGGCAGGGGCCACGTGAGG GAGACCCCGCGAGCATATGGGAAAGGGCAGTAGCGGGAGTCTGGCGAGGCAGGGGCCACGTGAGG A G KATNB1 Ensembl:ENSG00000140854 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57736185..57736357 26863196 MeRIP-seq:(Medium) rs1374594140 Functional Loss SNV dbSNP153 33..33 33 - - - 95330 RMVar_ID_95330 Human_SNP_ID_604225654 m1A Human chr16 - 57744736 57744731 57744737 AGACACACACATCCAAACACACATACATCCAAACACACACACACACACACCCGCACATCCCCCCA AGACACACACATCCAAACACACATACATCCA______CACACACACACACCCGCACATCCCCCCA GTGTGTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57744728..57744833 26863196 MeRIP-seq:(Medium) rs1256669231 Functional Loss DEL dbSNP153 32..37 33 - - - 95331 RMVar_ID_95331 Human_SNP_ID_604229750 m1A Human chr16 - 57758345 57758345 57758345 TATGGCTGGCAGAGGCAGCCAGCGGGTGGGGGATTCTGCTGCTCGCTCACCTGCCTGGCTCGCTG TATGGCTGGCAGAGGCAGCCAGCGGGTGGGGGGTTCTGCTGCTCGCTCACCTGCCTGGCTCGCTG T C KIFC3 Ensembl:ENSG00000140859 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:57758266..57758417;chr16:57758251..57759466 32194978 MeRIP-seq:(Medium) rs1555589832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762605,Human_RBP_ID_3947699,Human_RBP_ID_5237544,Human_RBP_ID_23209365,Human_RBP_ID_26445179,Human_RBP_ID_26757356 95332 RMVar_ID_95332 Human_SNP_ID_604229906 m1A Human chr16 - 57758701 57758701 57758701 GTCTCTCGGCTGTGGCTCTGAGTGCAAATTGCATGGGCGGAAAGGCGGGGGTGGCTGCTCTTCCT GTCTCTCGGCTGTGGCTCTGAGTGCAAATTGCGTGGGCGGAAAGGCGGGGGTGGCTGCTCTTCCT T C KIFC3 Ensembl:ENSG00000140859 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57758676..57758700 26863196 MeRIP-seq:(Medium) rs782679520 Functional Loss SNV dbSNP153 33..33 33 - - - 95333 RMVar_ID_95333 Human_SNP_ID_604229915 m1A Human chr16 + 57758721 57758721 57758721 CCTTTCCGCCCATGCAATTTGCACTCAGAGCCACAGCCGAGAGACACCGTTTCCTTCTGAACATG CCTTTCCGCCCATGCAATTTGCACTCAGAGCCGCAGCCGAGAGACACCGTTTCCTTCTGAACATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57758523..57758854 26863196 MeRIP-seq:(Medium) rs1555591471 Functional Loss SNV dbSNP153 33..33 33 - - - 95334 RMVar_ID_95334 Human_SNP_ID_604230630 m1A Human chr16 - 57760745 57760745 57760745 CCTGCTGCAGGATTCGCTTAGTGGTGACAGCAAGACCCTCATGGTGGTACAGGTGAGGACCTTGG CCTGCTGCAGGATTCGCTTAGTGGTGACAGCAGGACCCTCATGGTGGTACAGGTGAGGACCTTGG T C KIFC3 Ensembl:ENSG00000140859 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57760732..57760960 26863196 MeRIP-seq:(Medium) rs1309399371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128612,Human_RBP_ID_299476,Human_RBP_ID_3949263,Human_RBP_ID_18983836,Human_RBP_ID_19071653 Human_Splice_Rec_1719693,Human_Splice_Rec_1719731,Human_Splice_Rec_1719769,Human_Splice_Rec_1719775,Human_Splice_Rec_1719805,Human_Splice_Rec_1719843,Human_Splice_Rec_1719877,Human_Splice_Rec_1719911,Human_Splice_Rec_1719951,Human_Splice_Rec_1719987,Human_Splice_Rec_1720003 Human_miRNA_ID_2157904,Human_miRNA_ID_2611599 RMVar_hsa_circ_14674,RMVar_hsa_circ_119197,RMVar_hsa_circ_374406,RMVar_hsa_circ_178735,RMVar_hsa_circ_178736 95335 RMVar_ID_95335 Human_SNP_ID_604231307 m1A Human chr16 + 57762907 57762907 57762907 GGCATGCTCTGGCCTCTTGGCCTCAGCCCTGCAGCTCCCTCTGCCCCGGGTACTCCTCTGACCGC GGCATGCTCTGGCCTCTTGGCCTCAGCCCTGCGGCTCCCTCTGCCCCGGGTACTCCTCTGACCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57762905..57763013 26863196 MeRIP-seq:(Medium) rs1555599304 Functional Loss SNV dbSNP153 33..33 33 - - - 95336 RMVar_ID_95336 Human_SNP_ID_604232053 m1A Human chr16 + 57765567 57765567 57765567 ATGATGGAGTCGTCGTCGGCATCGAAAGTCACAGCATTGGTGGCCTCAGGTCCTTCCCCATCCTC ATGATGGAGTCGTCGTCGGCATCGAAAGTCACGGCATTGGTGGCCTCAGGTCCTTCCCCATCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:57765206..57765625;chr16:57765195..57765598 26863196 MeRIP-seq:(Medium) rs782779469 Functional Loss SNV dbSNP153 33..33 33 - - - 95337 RMVar_ID_95337 Human_SNP_ID_604232403 m1A Human chr16 - 57766948 57766948 57766948 CCAGGCCATCGAGGAGGTCAACAGCAACAACCAGGAGCTGCTGCGCAAGTACCGCCGCGAGCTGC CCAGGCCATCGAGGAGGTCAACAGCAACAACCGGGAGCTGCTGCGCAAGTACCGCCGCGAGCTGC T C KIFC3 Ensembl:ENSG00000140859 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:57766834..57767016;chr16:57766876..57767000 26863196 MeRIP-seq:(Medium) rs1555603533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_892219,Human_RBP_ID_9286310 Human_Splice_Rec_1719680,Human_Splice_Rec_1719681,Human_Splice_Rec_1719718,Human_Splice_Rec_1719719,Human_Splice_Rec_1719756,Human_Splice_Rec_1719757,Human_Splice_Rec_1719792,Human_Splice_Rec_1719793,Human_Splice_Rec_1719830,Human_Splice_Rec_1719831,Human_Splice_Rec_1719864,Human_Splice_Rec_1719865,Human_Splice_Rec_1719898,Human_Splice_Rec_1719899,Human_Splice_Rec_1719938,Human_Splice_Rec_1719939,Human_Splice_Rec_1719976,Human_Splice_Rec_1719977 RMVar_hsa_circ_119197,RMVar_hsa_circ_178736,RMVar_hsa_circ_50631,RMVar_hsa_circ_1967 95338 RMVar_ID_95338 Human_SNP_ID_604233161 m1A Human chr16 - 57769727 57769727 57769727 CCCCTCCCGCCTCACAGCCCGAGTGTCCCCATAGGCGTCCGGACCAACTTGCTGACCTTGCAGCC CCCCTCCCGCCTCACAGCCCGAGTGTCCCCATGGGCGTCCGGACCAACTTGCTGACCTTGCAGCC T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:57769701..57770725;chr16:57769706..57769798 26863196 MeRIP-seq:(Medium) rs1555605951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119197,RMVar_hsa_circ_178736,RMVar_hsa_circ_50631,RMVar_hsa_circ_1967,RMVar_hsa_circ_53254,RMVar_hsa_circ_335733 95339 RMVar_ID_95339 Human_SNP_ID_604233249 m1A Human chr16 + 57769920 57769920 57769920 TCCAGGGACTGCATCTCCTCCAGCATCTGCCCATGGGCCCGCTCCAGCTCTGACTCGTACATGGC TCCAGGGACTGCATCTCCTCCAGCATCTGCCCGTGGGCCCGCTCCAGCTCTGACTCGTACATGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57769801..57769981 26863196 MeRIP-seq:(Medium) rs782129947 Functional Loss SNV dbSNP153 33..33 33 - - - 95340 RMVar_ID_95340 Human_SNP_ID_604233250 m1A Human chr16 + 57769920 57769920 57769920 TCCAGGGACTGCATCTCCTCCAGCATCTGCCCATGGGCCCGCTCCAGCTCTGACTCGTACATGGC TCCAGGGACTGCATCTCCTCCAGCATCTGCCCTTGGGCCCGCTCCAGCTCTGACTCGTACATGGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57769801..57769981 26863196 MeRIP-seq:(Medium) rs782129947 Functional Loss SNV dbSNP153 33..33 33 - - - 95341 RMVar_ID_95341 Human_SNP_ID_604233802 m1A Human chr16 - 57771637 57771637 57771637 GAAGCACCGGGACCTGCTGATGGTGGAGAATGAGCGACTGAGGCAGGAGATGCGGCGCTGTGAGG GAAGCACCGGGACCTGCTGATGGTGGAGAATGGGCGACTGAGGCAGGAGATGCGGCGCTGTGAGG T C KIFC3 Ensembl:ENSG00000140859 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:57771405..57771718;chr16:57771500..57771719 26863196 MeRIP-seq:(Medium) rs376828844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3947706,Human_RBP_ID_9372881,Human_RBP_ID_18986393 Human_Splice_Rec_1719670,Human_Splice_Rec_1719671,Human_Splice_Rec_1719708,Human_Splice_Rec_1719709,Human_Splice_Rec_1719746,Human_Splice_Rec_1719747,Human_Splice_Rec_1719782,Human_Splice_Rec_1719783,Human_Splice_Rec_1719820,Human_Splice_Rec_1719821,Human_Splice_Rec_1719854,Human_Splice_Rec_1719855,Human_Splice_Rec_1719888,Human_Splice_Rec_1719889,Human_Splice_Rec_1719928,Human_Splice_Rec_1719929,Human_Splice_Rec_1719966,Human_Splice_Rec_1719967,Human_Splice_Rec_1720018,Human_Splice_Rec_1720019,Human_Splice_Rec_1720030,Human_Splice_Rec_1720031,Human_Splice_Rec_1720036,Human_Splice_Rec_1720037,Human_Splice_Rec_1720048,Human_Splice_Rec_1720049,Human_Splice_Rec_1720058,Human_Splice_Rec_1720059,Human_Splice_Rec_1720068,Human_Splice_Rec_1720069,Human_Splice_Rec_1720076,Human_Splice_Rec_1720084,Human_Splice_Rec_1720092,Human_Splice_Rec_1720096,Human_Splice_Rec_1720102,Human_Splice_Rec_1720110,Human_Splice_Rec_1720118 RMVar_hsa_circ_119197,RMVar_hsa_circ_178736,RMVar_hsa_circ_50631,RMVar_hsa_circ_1967,RMVar_hsa_circ_335733 95342 RMVar_ID_95342 Human_SNP_ID_604233966 m1A Human chr16 + 57772205 57772205 57772205 ACAAGGCAGGCCAGGCCCTGCGCTACCCCAGGACAGCCTTGTGGCCTCACCAGCTCAGATCGCAG ACAAGGCAGGCCAGGCCCTGCGCTACCCCAGGTCAGCCTTGTGGCCTCACCAGCTCAGATCGCAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57772201..57772275 26863196 MeRIP-seq:(Medium) rs1555609189 Functional Loss SNV dbSNP153 33..33 33 - - - 95343 RMVar_ID_95343 Human_SNP_ID_604238034 m1A Human chr16 + 57788586 57788586 57788586 TGGCGGGCAGGCCTGCTTTACCTGTATTCTCTACATTCATGGTGCCACCAGCTTCCCGGGCCTCC TGGCGGGCAGGCCTGCTTTACCTGTATTCTCTGCATTCATGGTGCCACCAGCTTCCCGGGCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57788580..57788675 26863196 MeRIP-seq:(Medium) rs1555618811 Functional Loss SNV dbSNP153 33..33 33 - - - 95344 RMVar_ID_95344 Human_SNP_ID_604239785 m1A Human chr16 - 57795143 57795143 57795143 GGAGTGTCTCACCTATCTCTCTGTCCTGGGACAGGGCGTGGAAAAGATACCCCAGTCTGCGGTGA GGAGTGTCTCACCTATCTCTCTGTCCTGGGACTGGGCGTGGAAAAGATACCCCAGTCTGCGGTGA T A KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57795101..57795150 26863196 MeRIP-seq:(Medium) rs1333073508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22653128 95345 RMVar_ID_95345 Human_SNP_ID_604239786 m1A Human chr16 - 57795143 57795143 57795143 GGAGTGTCTCACCTATCTCTCTGTCCTGGGACAGGGCGTGGAAAAGATACCCCAGTCTGCGGTGA GGAGTGTCTCACCTATCTCTCTGTCCTGGGACGGGGCGTGGAAAAGATACCCCAGTCTGCGGTGA T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:57795101..57795150 26863196 MeRIP-seq:(Medium) rs1333073508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22653128 95346 RMVar_ID_95346 Human_SNP_ID_604291613 m1A Human chr16 + 57995013 57995013 57995013 TGGCCACAGGAAGGAACTCAGTCAGACAGAGGAGGTGGGCGTGGCTGGTCAGCCTTCTTACGGTG TGGCCACAGGAAGGAACTCAGTCAGACAGAGGGGGTGGGCGTGGCTGGTCAGCCTTCTTACGGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:57994963..57995094 26863196 MeRIP-seq:(Medium) rs937423967 Functional Loss SNV dbSNP153 33..33 33 - - - 95347 RMVar_ID_95347 Human_SNP_ID_604291877 m1A Human chr16 + 57996071 57996071 57996071 CCACACGGCAACTGATGCCTTACACCTAGCCCACCTCTGGGGCCCCAGCCCCACCATGAGCCTCC CCACACGGCAACTGATGCCTTACACCTAGCCCGCCTCTGGGGCCCCAGCCCCACCATGAGCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57996027..57996136 26863196 MeRIP-seq:(Medium) rs1294903567 Functional Loss SNV dbSNP153 33..33 33 - - - 95348 RMVar_ID_95348 Human_SNP_ID_604291908 m1A Human chr16 + 57996182 57996182 57996182 TGGGCTGGCATCACACCCTCCTTAGGGCAGGGAGAAGCCACTTGACTTCCAGCCTGGCTCCAGTG TGGGCTGGCATCACACCCTCCTTAGGGCAGGGGGAAGCCACTTGACTTCCAGCCTGGCTCCAGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57996058..57996407 32194978 MeRIP-seq:(Medium) rs529359264 Functional Loss SNV dbSNP153 33..33 33 - - - 95349 RMVar_ID_95349 Human_SNP_ID_604292194 m1A Human chr16 - 57996904 57996904 57996904 CAGAAGCACCAGCTGGCCCACTGTGCGGCGGCAGAGAAGCCCCTGCGCTGCACGCTTTGCGAACG CAGAAGCACCAGCTGGCCCACTGTGCGGCGGCGGAGAAGCCCCTGCGCTGCACGCTTTGCGAACG T C ZNF319 Ensembl:ENSG00000166188 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57996853..57997003 32194978 MeRIP-seq:(Medium) rs757245099 Functional Loss SNV dbSNP153 33..33 33 - - - 95350 RMVar_ID_95350 Human_SNP_ID_604293959 m1A Human chr16 + 58002428 58002428 58002428 GGGGTTACAACTTTTGTGGTATATACAAAGGTAGAGAATGCTAACAGGATAAATGTACTCATTTT GGGGTTACAACTTTTGTGGTATATACAAAGGTGGAGAATGCTAACAGGATAAATGTACTCATTTT A G USB1 Ensembl:ENSG00000103005 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58002425..58002685 26863196 MeRIP-seq:(Medium) rs562589210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85931,RMVar_hsa_circ_178740 95351 RMVar_ID_95351 Human_SNP_ID_604297237 m1A Human chr16 + 58016018 58016018 58016018 GAGGCATGACCTGATCTATATCTGGGGATGTCAGTCTGGCTAGTGGTGTGTCTGTGGCCATGGAG GAGGCATGACCTGATCTATATCTGGGGATGTCGGTCTGGCTAGTGGTGTGTCTGTGGCCATGGAG A G USB1 Ensembl:ENSG00000103005 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:58015967..58016051 26863196 MeRIP-seq:(Medium) rs1027173018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23693860 RMVar_hsa_circ_83965,RMVar_hsa_circ_85931,RMVar_hsa_circ_178740,RMVar_hsa_circ_23230,RMVar_hsa_circ_8193,RMVar_hsa_circ_178743,RMVar_hsa_circ_376785,RMVar_hsa_circ_178744 95352 RMVar_ID_95352 Human_SNP_ID_604298306 m1A Human chr16 - 58020451 58020449 58020452 AGAGGAAGAGAGACAGAGGAGAGAAAGAGAGGAGAAGAGAGAGAAAGAAGAGGAAGAGAAAGAGA AGAGGAAGAGAGACAGAGGAGAGAAAGAGAG___AAGAGAGAGAAAGAAGAGGAAGAGAAAGAGA TCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58020400..58020522 26863196 MeRIP-seq:(Medium) rs752765084 Functional Loss DEL dbSNP153 32..34 33 - - - 95353 RMVar_ID_95353 Human_SNP_ID_604298455 m1A Human chr16 - 58020646 58020634 58020646 AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGAAGAGAGAGAGGAGAGGAAGAGAGAGGAGGGGAG AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGA____________GAGGAAGAGAGAGGAGGGGAG CTCCTCTCTCTCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58020599..58020732 26863196 MeRIP-seq:(Medium) rs1392464356 Functional Loss DEL dbSNP153 33..44 33 - - - 95354 RMVar_ID_95354 Human_SNP_ID_604298459 m1A Human chr16 - 58020646 58020643 58020646 AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGAAGAGAGAGAGGAGAGGAAGAGAGAGGAGGGGAG AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGA___GAGAGAGGAGAGGAAGAGAGAGGAGGGGAG CTCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58020599..58020732 26863196 MeRIP-seq:(Medium) rs1567424890 Functional Loss DEL dbSNP153 33..35 33 - - - 95355 RMVar_ID_95355 Human_SNP_ID_604298460 m1A Human chr16 - 58020646 58020646 58020646 AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGAAGAGAGAGAGGAGAGGAAGAGAGAGGAGGGGAG AGAGAGACAGGAAGGGAAGAGAGAGGAGAGGATGAGAGAGAGGAGAGGAAGAGAGAGGAGGGGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58020599..58020732 26863196 MeRIP-seq:(Medium) rs1323051521 Functional Loss SNV dbSNP153 33..33 33 - - - 95356 RMVar_ID_95356 Human_SNP_ID_604299783 m1A Human chr16 - 58025830 58025830 58025830 GGGAGCCGACCCGAGAGAGCGAGCGAGAGAGCAAGCGAGCCAGCCAAGGAGCGGGCGCCCGACGT GGGAGCCGACCCGAGAGAGCGAGCGAGAGAGCGAGCGAGCCAGCCAAGGAGCGGGCGCCCGACGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58025781..58026015 26863196 MeRIP-seq:(Medium) rs1000024926 Functional Loss SNV dbSNP153 33..33 33 - - - 95357 RMVar_ID_95357 Human_SNP_ID_604299922 m1A Human chr16 - 58026220 58026220 58026220 GCCGCGGACCTCGGGCTCCCGGTCCCCGCCGGAGCCGCCTAGGTCGCCTCGGCAAATTCCCAAGC GCCGCGGACCTCGGGCTCCCGGTCCCCGCCGGGGCCGCCTAGGTCGCCTCGGCAAATTCCCAAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58026171..58026352 26863196 MeRIP-seq:(Medium) rs1051811071 Functional Loss SNV dbSNP153 33..33 33 - - - 95358 RMVar_ID_95358 Human_SNP_ID_604304338 m1A Human chr16 - 58041708 58041708 58041708 TCTGGCTTCCCACCTGGGGGTGGTGGCTGGGGAGGCCGGGGCGGCCGGTGGTCAGGCCGGCCTGG TCTGGCTTCCCACCTGGGGGTGGTGGCTGGGGTGGCCGGGGCGGCCGGTGGTCAGGCCGGCCTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr16:58041661..58041763;chr16:58041631..58041721 26863196,26863410 MeRIP-seq:(Medium) rs774601548 Functional Loss SNV dbSNP153 33..33 33 - - - 95359 RMVar_ID_95359 Human_SNP_ID_604304339 m1A Human chr16 - 58041708 58041708 58041708 TCTGGCTTCCCACCTGGGGGTGGTGGCTGGGGAGGCCGGGGCGGCCGGTGGTCAGGCCGGCCTGG TCTGGCTTCCCACCTGGGGGTGGTGGCTGGGGCGGCCGGGGCGGCCGGTGGTCAGGCCGGCCTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr16:58041661..58041763;chr16:58041631..58041721 26863196,26863410 MeRIP-seq:(Medium) rs774601548 Functional Loss SNV dbSNP153 33..33 33 - - - 95360 RMVar_ID_95360 Human_SNP_ID_604305506 m1A Human chr16 + 58045299 58045299 58045299 AGCCGCGTGGTGGTGCAGATGGAGGAGGTGGCACGGACGGTGAACGTGGTGATGGTGCTGGTGCC AGCCGCGTGGTGGTGCAGATGGAGGAGGTGGCCCGGACGGTGAACGTGGTGATGGTGCTGGTGCC A C MMP15 Ensembl:ENSG00000102996 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:58045248..58045398 26863196 MeRIP-seq:(Medium) rs372006759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2172235 RMVar_hsa_circ_97048,RMVar_hsa_circ_178748,RMVar_hsa_circ_99441,RMVar_hsa_circ_178749,RMVar_hsa_circ_178750,RMVar_hsa_circ_118632,RMVar_hsa_circ_178751,RMVar_hsa_circ_76167 95361 RMVar_ID_95361 Human_SNP_ID_604305510 m1A Human chr16 + 58045303 58045303 58045303 GCGTGGTGGTGCAGATGGAGGAGGTGGCACGGACGGTGAACGTGGTGATGGTGCTGGTGCCACTG GCGTGGTGGTGCAGATGGAGGAGGTGGCACGGGCGGTGAACGTGGTGATGGTGCTGGTGCCACTG A G MMP15 Ensembl:ENSG00000102996 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58045253..58045318 26863196 MeRIP-seq:(Medium) rs763008598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2172235 RMVar_hsa_circ_97048,RMVar_hsa_circ_178748,RMVar_hsa_circ_99441,RMVar_hsa_circ_178749,RMVar_hsa_circ_178750,RMVar_hsa_circ_118632,RMVar_hsa_circ_178751,RMVar_hsa_circ_76167 95362 RMVar_ID_95362 Human_SNP_ID_604305870 m1A Human chr16 + 58046455 58046455 58046455 GGGGTTCCTCCCCTCCAGCTCCCTGTGCCCCCAGGGTCCTGGGAGGAGAGACACTGGTGGGGATA GGGGTTCCTCCCCTCCAGCTCCCTGTGCCCCCGGGGTCCTGGGAGGAGAGACACTGGTGGGGATA A G MMP15 Ensembl:ENSG00000102996 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:58046304..58046851 32194978 MeRIP-seq:(Medium) rs945454629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476277 RMVar_hsa_circ_97048,RMVar_hsa_circ_178748,RMVar_hsa_circ_99441,RMVar_hsa_circ_178749,RMVar_hsa_circ_178750,RMVar_hsa_circ_118632,RMVar_hsa_circ_178751,RMVar_hsa_circ_76167 95363 RMVar_ID_95363 Human_SNP_ID_604335117 m1A Human chr16 - 58160070 58160070 58160070 GTTAATAACATGCTTCTGAGCTATGTGGATGTATAAATGAAAACACCCCCAACTAGGTATTGTAG GTTAATAACATGCTTCTGAGCTATGTGGATGTGTAAATGAAAACACCCCCAACTAGGTATTGTAG T C CSNK2A2 Ensembl:ENSG00000070770 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:58160026..58160275 32194978 MeRIP-seq:(Medium) rs960331127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476322,Human_RBP_ID_1519786,Human_RBP_ID_8435791,Human_RBP_ID_18286194,Human_RBP_ID_21888888,Human_RBP_ID_23693929 Human_miRNA_ID_1784920 RMVar_hsa_circ_178752 95364 RMVar_ID_95364 Human_SNP_ID_604344553 m1A Human chr16 + 58197683 58197683 58197683 GCCTCGTAGTCCCAGTACTCGCGGCTCCTCAGACTGTTCACCTCGGCGTAGACCCGGGCCCTGCT GCCTCGTAGTCCCAGTACTCGCGGCTCCTCAGCCTGTTCACCTCGGCGTAGACCCGGGCCCTGCT A C AC009107.1 Ensembl:ENSG00000260867 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:58197626..58197775 32194978 MeRIP-seq:(Medium) rs576968089 Functional Loss SNV dbSNP153 33..33 33 - - - 95365 RMVar_ID_95365 Human_SNP_ID_604344554 m1A Human chr16 + 58197683 58197683 58197683 GCCTCGTAGTCCCAGTACTCGCGGCTCCTCAGACTGTTCACCTCGGCGTAGACCCGGGCCCTGCT GCCTCGTAGTCCCAGTACTCGCGGCTCCTCAGGCTGTTCACCTCGGCGTAGACCCGGGCCCTGCT A G AC009107.1 Ensembl:ENSG00000260867 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:58197626..58197775 32194978 MeRIP-seq:(Medium) rs576968089 Functional Loss SNV dbSNP153 33..33 33 - - - 95366 RMVar_ID_95366 Human_SNP_ID_604344572 m1A Human chr16 + 58197747 58197747 58197747 TGCCCGCGGCCGGGCCGGGCATGGCGGGCGGGACCGGGGGGCGGCGCGGGGCGCAGAGGGTGGCG TGCCCGCGGCCGGGCCGGGCATGGCGGGCGGGGCCGGGGGGCGGCGCGGGGCGCAGAGGGTGGCG A G AC009107.1 Ensembl:ENSG00000260867 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:58197713..58197878 26863196 MeRIP-seq:(Medium) rs887497202 Functional Loss SNV dbSNP153 33..33 33 - - - 95367 RMVar_ID_95367 Human_SNP_ID_604357176 m1A Human chr16 + 58250049 58250049 58250049 GACTGATGATGAGTCCGAGAGCGTCCTCTCCGACTCCCATGAAGGGTCGGAGCTGGAGCTGCCTG GACTGATGATGAGTCCGAGAGCGTCCTCTCCGTCTCCCATGAAGGGTCGGAGCTGGAGCTGCCTG A T CCDC113 Ensembl:ENSG00000103021 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58249999..58250079 26863196 MeRIP-seq:(Medium) rs952410327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1720677,Human_Splice_Rec_1720691,Human_Splice_Rec_1720707,Human_Splice_Rec_1720713 95368 RMVar_ID_95368 Human_SNP_ID_604364355 m1A Human chr16 + 58279707 58279707 58279707 TTTTTTTTTTTTGCAGATGTCCTTAAAAGGCCATCGTAAGGCTTGGAATCGAATGAAAATAACCA TTTTTTTTTTTTGCAGATGTCCTTAAAAGGCCGTCGTAAGGCTTGGAATCGAATGAAAATAACCA A G CCDC113 Ensembl:ENSG00000103021 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:58279701..58279800 32194978 MeRIP-seq:(Medium) rs770794619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1720690,Human_Splice_Rec_1720706 95369 RMVar_ID_95369 Human_SNP_ID_604390963 m1A Human chr16 - 58392523 58392523 58392523 GCCTCAGGAGTTAGGGGTGTACAAGACGGGGAAGCGGAGACTGGGCAGGATGGTTGGGGTCAGGA GCCTCAGGAGTTAGGGGTGTACAAGACGGGGAGGCGGAGACTGGGCAGGATGGTTGGGGTCAGGA T C AC009118.2 Ensembl:ENSG00000276131 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:58392476..58392762;chr16:58392444..58392699 26863196 MeRIP-seq:(Medium) rs971019267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_277607,Human_RBP_ID_1131229,Human_RBP_ID_5576113 95370 RMVar_ID_95370 Human_SNP_ID_604390974 m1A Human chr16 + 58392552 58392552 58392552 CGCTTCCCCGTCTTGTACACCCCTAACTCCTGAGGCTCCTCCGAATCACGCGAGTGGAAGCGGAG CGCTTCCCCGTCTTGTACACCCCTAACTCCTGGGGCTCCTCCGAATCACGCGAGTGGAAGCGGAG A G GINS3 Ensembl:ENSG00000181938 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:58392502..58392695 26863196 MeRIP-seq:(Medium) rs756801247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1366048,Human_RBP_ID_1519844 95371 RMVar_ID_95371 Human_SNP_ID_604391021 m1A Human chr16 - 58392639 58392639 58392639 CGTCCAAAGAAAGAAAGTTCTCCTCAGGCCCCAGCGCACCCGACTCCACTCGGAAATAAGCCTCT CGTCCAAAGAAAGAAAGTTCTCCTCAGGCCCCTGCGCACCCGACTCCACTCGGAAATAAGCCTCT T A AC009118.2 Ensembl:ENSG00000276131 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:58392476..58392643 32194978 MeRIP-seq:(Medium) rs1159126126 Functional Loss SNV dbSNP153 33..33 33 - - - 95372 RMVar_ID_95372 Human_SNP_ID_604420213 m1A Human chr16 + 58503952 58503952 58503952 CTCAGTCAGCCCTCCTCTGCCTCCCATCAGCCAGAGCGGTGAGGCCCCCCACCCTCCCCACAGGG CTCAGTCAGCCCTCCTCTGCCTCCCATCAGCCCGAGCGGTGAGGCCCCCCACCCTCCCCACAGGG A C NDRG4 Ensembl:ENSG00000103034 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58503901..58504073 26863196 MeRIP-seq:(Medium) rs771737366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1721325 RMVar_hsa_circ_7134,RMVar_hsa_circ_20750,RMVar_hsa_circ_2587 95373 RMVar_ID_95373 Human_SNP_ID_604424544 m1A Human chr16 - 58515882 58515882 58515882 CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCACCTTGGGACTCAGCTCCAGCCCCACCCGCCGG CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCTCCTTGGGACTCAGCTCCAGCCCCACCCGCCGG T A lnc-CNOT1-3 RNACentral:URS00009B655F lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:58515765..58516073 26863196 MeRIP-seq:(Medium) rs1046247861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4374946,Human_RBP_ID_12764584 95374 RMVar_ID_95374 Human_SNP_ID_604424545 m1A Human chr16 - 58515882 58515882 58515882 CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCACCTTGGGACTCAGCTCCAGCCCCACCCGCCGG CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCCCCTTGGGACTCAGCTCCAGCCCCACCCGCCGG T G lnc-CNOT1-3 RNACentral:URS00009B655F lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:58515765..58516073 26863196 MeRIP-seq:(Medium) rs1046247861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4374946,Human_RBP_ID_12764584 95375 RMVar_ID_95375 Human_SNP_ID_604424548 m1A Human chr16 + 58515888 58515888 58515888 GGTGGGGCTGGAGCTGAGTCCCAAGGTGAGCGAGCGAGCCGGCGGGCGGAGGACCCGCGGCGGGG GGTGGGGCTGGAGCTGAGTCCCAAGGTGAGCGGGCGAGCCGGCGGGCGGAGGACCCGCGGCGGGG A G SETD6 Ensembl:ENSG00000103037 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:58515770..58516002 26863196 MeRIP-seq:(Medium) rs186683751 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5358200,Human_RBP_ID_9372884,Human_RBP_ID_18983848,Human_RBP_ID_19071679,Human_RBP_ID_22442100,Human_RBP_ID_22945091 Human_Splice_Rec_1721516,Human_Splice_Rec_1721532,Human_Splice_Rec_1721548,Human_Splice_Rec_1721564,Human_Splice_Rec_1721576,Human_Splice_Rec_1721584,Human_Splice_Rec_1721600 95376 RMVar_ID_95376 Human_SNP_ID_604424843 m1A Human chr16 - 58516192 58516192 58516192 CTGGCTCTGCAGCGCAACTCGCTCTGAGGAAGACACAGGTGTGAGCGCCCCGGCGCGGCCTCGCG CTGGCTCTGCAGCGCAACTCGCTCTGAGGAAGTCACAGGTGTGAGCGCCCCGGCGCGGCCTCGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58516189..58516288 26863196 MeRIP-seq:(Medium) rs780786816 Functional Loss SNV dbSNP153 33..33 33 - - - 95377 RMVar_ID_95377 Human_SNP_ID_604425841 m1A Human chr16 + 58518518 58518501 58518519 CTTTGTGATAGGGAGGGAGGAGGTGCTGACTGAAGAGGAGCTGACCACCACACTAAAGGTAAACG CTTTGTGATAGGGAGG__________________GAGGAGCTGACCACCACACTAAAGGTAAACG GGAGGAGGTGCTGACTGAA G SETD6 Ensembl:ENSG00000103037 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:58518412..58518742 26863196 MeRIP-seq:(Medium) rs759344297 Functional Loss DEL dbSNP153,HGVD 17..34 33 - - - Human_RBP_ID_762422,Human_RBP_ID_18986411,Human_RBP_ID_22356103,Human_RBP_ID_22541635,Human_RBP_ID_23694240,Human_RBP_ID_26329056 Human_Splice_Rec_1721529,Human_Splice_Rec_1721545,Human_Splice_Rec_1721561,Human_Splice_Rec_1721581,Human_Splice_Rec_1721595,Human_Splice_Rec_1721623,Human_Splice_Rec_1721629,Human_Splice_Rec_1721631 95378 RMVar_ID_95378 Human_SNP_ID_604425849 m1A Human chr16 + 58518521 58518521 58518521 TGTGATAGGGAGGGAGGAGGTGCTGACTGAAGAGGAGCTGACCACCACACTAAAGGTAAACGGCT TGTGATAGGGAGGGAGGAGGTGCTGACTGAAGGGGAGCTGACCACCACACTAAAGGTAAACGGCT A G SETD6 Ensembl:ENSG00000103037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58518431..58518850 26863196 MeRIP-seq:(Medium) rs1399376698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762422,Human_RBP_ID_18986411,Human_RBP_ID_22356103,Human_RBP_ID_23694240,Human_RBP_ID_26329056 Human_Splice_Rec_1721529,Human_Splice_Rec_1721545,Human_Splice_Rec_1721561,Human_Splice_Rec_1721581,Human_Splice_Rec_1721595,Human_Splice_Rec_1721623,Human_Splice_Rec_1721629,Human_Splice_Rec_1721631 95379 RMVar_ID_95379 Human_SNP_ID_604433352 m1A Human chr16 - 58546281 58546281 58546281 TGCTAATTAGTCAAGGAAGGCTTCTGTTAGCTAGGATACTATCTTAAATGGTACTTGTCCATGTA TGCTAATTAGTCAAGGAAGGCTTCTGTTAGCTTGGATACTATCTTAAATGGTACTTGTCCATGTA T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58546277..58546350 26863196 MeRIP-seq:(Medium) rs200170988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8435947,Human_RBP_ID_19071690,Human_RBP_ID_22356383 RMVar_hsa_circ_78442,RMVar_hsa_circ_178761,RMVar_hsa_circ_84121,RMVar_hsa_circ_370790,RMVar_hsa_circ_24528,RMVar_hsa_circ_2249,RMVar_hsa_circ_4098,RMVar_hsa_circ_31122,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,RMVar_hsa_circ_178762,RMVar_hsa_circ_178763,RMVar_hsa_circ_93605,RMVar_hsa_circ_178765,RMVar_hsa_circ_178767,RMVar_hsa_circ_178766,RMVar_hsa_circ_178768,RMVar_hsa_circ_122630,RMVar_hsa_circ_114911,RMVar_hsa_circ_83846,RMVar_hsa_circ_119415,RMVar_hsa_circ_178770,RMVar_hsa_circ_178769,RMVar_hsa_circ_102421,RMVar_hsa_circ_122725,RMVar_hsa_circ_178776,RMVar_hsa_circ_178775,RMVar_hsa_circ_102357,RMVar_hsa_circ_178778,RMVar_hsa_circ_178779,RMVar_hsa_circ_82830,RMVar_hsa_circ_43758,RMVar_hsa_circ_114456,RMVar_hsa_circ_178780,RMVar_hsa_circ_178783,RMVar_hsa_circ_178785,RMVar_hsa_circ_123204,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_372173,RMVar_hsa_circ_2239,RMVar_hsa_circ_64557,RMVar_hsa_circ_128166,RMVar_hsa_circ_178787,RMVar_hsa_circ_117889,RMVar_hsa_circ_99183,RMVar_hsa_circ_178789,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_370285,RMVar_hsa_circ_119647,RMVar_hsa_circ_178792,RMVar_hsa_circ_178793,RMVar_hsa_circ_178791,RMVar_hsa_circ_178794,RMVar_hsa_circ_376794,RMVar_hsa_circ_51596,RMVar_hsa_circ_43614,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178795,RMVar_hsa_circ_178796,RMVar_hsa_circ_178797,RMVar_hsa_circ_374418,RMVar_hsa_circ_105657,RMVar_hsa_circ_178798,RMVar_hsa_circ_373866,RMVar_hsa_circ_85142,RMVar_hsa_circ_178800,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_178801,RMVar_hsa_circ_178799,RMVar_hsa_circ_98400,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178805,RMVar_hsa_circ_178803 95380 RMVar_ID_95380 Human_SNP_ID_604433353 m1A Human chr16 - 58546281 58546281 58546281 TGCTAATTAGTCAAGGAAGGCTTCTGTTAGCTAGGATACTATCTTAAATGGTACTTGTCCATGTA TGCTAATTAGTCAAGGAAGGCTTCTGTTAGCTGGGATACTATCTTAAATGGTACTTGTCCATGTA T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:58546277..58546350 26863196 MeRIP-seq:(Medium) rs200170988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8435947,Human_RBP_ID_19071690,Human_RBP_ID_22356383 RMVar_hsa_circ_78442,RMVar_hsa_circ_178761,RMVar_hsa_circ_84121,RMVar_hsa_circ_370790,RMVar_hsa_circ_24528,RMVar_hsa_circ_2249,RMVar_hsa_circ_4098,RMVar_hsa_circ_31122,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,RMVar_hsa_circ_178762,RMVar_hsa_circ_178763,RMVar_hsa_circ_93605,RMVar_hsa_circ_178765,RMVar_hsa_circ_178767,RMVar_hsa_circ_178766,RMVar_hsa_circ_178768,RMVar_hsa_circ_122630,RMVar_hsa_circ_114911,RMVar_hsa_circ_83846,RMVar_hsa_circ_119415,RMVar_hsa_circ_178770,RMVar_hsa_circ_178769,RMVar_hsa_circ_102421,RMVar_hsa_circ_122725,RMVar_hsa_circ_178776,RMVar_hsa_circ_178775,RMVar_hsa_circ_102357,RMVar_hsa_circ_178778,RMVar_hsa_circ_178779,RMVar_hsa_circ_82830,RMVar_hsa_circ_43758,RMVar_hsa_circ_114456,RMVar_hsa_circ_178780,RMVar_hsa_circ_178783,RMVar_hsa_circ_178785,RMVar_hsa_circ_123204,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_372173,RMVar_hsa_circ_2239,RMVar_hsa_circ_64557,RMVar_hsa_circ_128166,RMVar_hsa_circ_178787,RMVar_hsa_circ_117889,RMVar_hsa_circ_99183,RMVar_hsa_circ_178789,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_370285,RMVar_hsa_circ_119647,RMVar_hsa_circ_178792,RMVar_hsa_circ_178793,RMVar_hsa_circ_178791,RMVar_hsa_circ_178794,RMVar_hsa_circ_376794,RMVar_hsa_circ_51596,RMVar_hsa_circ_43614,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178795,RMVar_hsa_circ_178796,RMVar_hsa_circ_178797,RMVar_hsa_circ_374418,RMVar_hsa_circ_105657,RMVar_hsa_circ_178798,RMVar_hsa_circ_373866,RMVar_hsa_circ_85142,RMVar_hsa_circ_178800,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_178801,RMVar_hsa_circ_178799,RMVar_hsa_circ_98400,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178805,RMVar_hsa_circ_178803 95381 RMVar_ID_95381 Human_SNP_ID_604434664 m1A Human chr16 - 58551670 58551670 58551670 GCTCCTCTTGCTGGTCAAGTTAGCACTATGGTAACCACCTCAACAACTACCACTGTTGCTAAAAC GCTCCTCTTGCTGGTCAAGTTAGCACTATGGTCACCACCTCAACAACTACCACTGTTGCTAAAAC T G CNOT1 Ensembl:ENSG00000125107 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:58551651..58551675 26863196 MeRIP-seq:(Medium) rs916524281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1520010,Human_RBP_ID_8435963,Human_RBP_ID_9285104,Human_RBP_ID_17254833,Human_RBP_ID_17370280,Human_RBP_ID_17878762,Human_RBP_ID_18681334,Human_RBP_ID_26810406 Human_Splice_Rec_1721677,Human_Splice_Rec_1721789,Human_Splice_Rec_1721885,Human_Splice_Rec_1722015,Human_Splice_Rec_1722037 Human_miRNA_ID_2582338,Human_miRNA_ID_2582339 RMVar_hsa_circ_78442,RMVar_hsa_circ_178761,RMVar_hsa_circ_84121,RMVar_hsa_circ_370790,RMVar_hsa_circ_24528,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,RMVar_hsa_circ_178762,RMVar_hsa_circ_178763,RMVar_hsa_circ_93605,RMVar_hsa_circ_178765,RMVar_hsa_circ_178767,RMVar_hsa_circ_178766,RMVar_hsa_circ_178768,RMVar_hsa_circ_122630,RMVar_hsa_circ_114911,RMVar_hsa_circ_83846,RMVar_hsa_circ_119415,RMVar_hsa_circ_178770,RMVar_hsa_circ_178769,RMVar_hsa_circ_122725,RMVar_hsa_circ_178776,RMVar_hsa_circ_102357,RMVar_hsa_circ_178778,RMVar_hsa_circ_178779,RMVar_hsa_circ_82830,RMVar_hsa_circ_114456,RMVar_hsa_circ_178780,RMVar_hsa_circ_178783,RMVar_hsa_circ_178785,RMVar_hsa_circ_123204,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_372173,RMVar_hsa_circ_128166,RMVar_hsa_circ_178787,RMVar_hsa_circ_117889,RMVar_hsa_circ_99183,RMVar_hsa_circ_178789,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_370285,RMVar_hsa_circ_119647,RMVar_hsa_circ_178792,RMVar_hsa_circ_178791,RMVar_hsa_circ_178794,RMVar_hsa_circ_376794,RMVar_hsa_circ_43614,RMVar_hsa_circ_9408,RMVar_hsa_circ_62732,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178795,RMVar_hsa_circ_178796,RMVar_hsa_circ_178797,RMVar_hsa_circ_374418,RMVar_hsa_circ_105657,RMVar_hsa_circ_178798,RMVar_hsa_circ_373866,RMVar_hsa_circ_85142,RMVar_hsa_circ_178800,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_178801,RMVar_hsa_circ_178799,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_99570,RMVar_hsa_circ_912,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_37158,RMVar_hsa_circ_178807,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_72289,RMVar_hsa_circ_370564,RMVar_hsa_circ_109818,RMVar_hsa_circ_178811,RMVar_hsa_circ_41176,RMVar_hsa_circ_30056,RMVar_hsa_circ_61488,RMVar_hsa_circ_72999,RMVar_hsa_circ_298945,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_62453,RMVar_hsa_circ_47580,RMVar_hsa_circ_178813,RMVar_hsa_circ_178814,RMVar_hsa_circ_93968,RMVar_hsa_circ_110381,RMVar_hsa_circ_368445,RMVar_hsa_circ_178815,RMVar_hsa_circ_336655,RMVar_hsa_circ_73537,RMVar_hsa_circ_178816,RMVar_hsa_circ_178817 95382 RMVar_ID_95382 Human_SNP_ID_604456349 m1A Human chr16 + 58629792 58629770 58629793 AACTCCTGGGTCCCCGACTCCGGCTCTCCTCGACCCCCTCTTCGGTTAACTCCGCTTGTTTCTCT AACTCCTGGGT_______________________CCCCTCTTCGGTTAACTCCGCTTGTTTCTCT TCCCCGACTCCGGCTCTCCTCGAC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:58629491..58629793 26863196 MeRIP-seq:(Medium) rs1309538217 Functional Loss DEL dbSNP153 12..34 33 - - - 95383 RMVar_ID_95383 Human_SNP_ID_604456353 m1A Human chr16 - 58629778 58629778 58629778 AGTTAACCGAAGAGGGGGTCGAGGAGAGCCGGAGTCGGGGACCCAGGAGTTTCCTGTGTCCAGCG AGTTAACCGAAGAGGGGGTCGAGGAGAGCCGGCGTCGGGGACCCAGGAGTTTCCTGTGTCCAGCG T G CNOT1 Ensembl:ENSG00000125107 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:58629487..58629827 26863196 MeRIP-seq:(Medium) rs1392340360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44674,Human_RBP_ID_233584,Human_RBP_ID_818074,Human_RBP_ID_4375448,Human_RBP_ID_6524386,Human_RBP_ID_8808810,Human_RBP_ID_18681435,Human_RBP_ID_22442562,Human_RBP_ID_23694504,Human_RBP_ID_24544710,Human_RBP_ID_26330139,Human_RBP_ID_26946539 Human_Splice_Rec_1721633,Human_Splice_Rec_1721745,Human_Splice_Rec_1721841,Human_Splice_Rec_1721971,Human_Splice_Rec_1722075,Human_Splice_Rec_1722089,Human_Splice_Rec_1722093,Human_Splice_Rec_1722097,Human_Splice_Rec_1722101,Human_Splice_Rec_1722107 Human_miRNA_ID_2040918,Human_miRNA_ID_3019902 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 95384 RMVar_ID_95384 Human_SNP_ID_604479217 m1A Human chr16 - 58718593 58718593 58718593 CCCATCTTCAGGGATGCTGGCATGCAGCTACAAGGTTATCGGTATTATGACCCCAAGACTTGCGG CCCATCTTCAGGGATGCTGGCATGCAGCTACAGGGTTATCGGTATTATGACCCCAAGACTTGCGG T C GOT2 Ensembl:ENSG00000125166 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:58718518..58721662 32194978 MeRIP-seq:(Medium) rs572936213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_476631,Human_RBP_ID_27443811 Human_Splice_Rec_1722280,Human_Splice_Rec_1722281,Human_Splice_Rec_1722296,Human_Splice_Rec_1722297,Human_Splice_Rec_1722316,Human_Splice_Rec_1722317,Human_Splice_Rec_1722328,Human_Splice_Rec_1722334 Human_miRNA_ID_2508113 RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_3579,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178881,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_7691,RMVar_hsa_circ_178888,RMVar_hsa_circ_281956,RMVar_hsa_circ_328817,RMVar_hsa_circ_366063,RMVar_hsa_circ_178889,RMVar_hsa_circ_274531,RMVar_hsa_circ_178890,RMVar_hsa_circ_178891,RMVar_hsa_circ_22398 95385 RMVar_ID_95385 Human_SNP_ID_604482945 m1A Human chr16 - 58734238 58734238 58734238 TGCTCCGTCCTGCGGCTGCCCACTGCCCTCCTACGGTCCACCATGGCCCTGCTGCACTCCGGCCG TGCTCCGTCCTGCGGCTGCCCACTGCCCTCCTGCGGTCCACCATGGCCCTGCTGCACTCCGGCCG T C GOT2 Ensembl:ENSG00000125166 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:58734166..58734325 26863196 MeRIP-seq:(Medium) rs933373283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233589,Human_RBP_ID_817768,Human_RBP_ID_894883,Human_RBP_ID_4375605,Human_RBP_ID_5419471,Human_RBP_ID_5495874,Human_RBP_ID_8436112,Human_RBP_ID_9325145,Human_RBP_ID_17878846,Human_RBP_ID_22441039,Human_RBP_ID_27243528 Human_Splice_Rec_1722273,Human_Splice_Rec_1722291,Human_Splice_Rec_1722309,Human_Splice_Rec_1722321,Human_Splice_Rec_1722329,Human_Splice_Rec_1722335 Human_miRNA_ID_2574372,Human_miRNA_ID_3074464 RMVar_hsa_circ_103390,RMVar_hsa_circ_178878 95386 RMVar_ID_95386 Human_SNP_ID_604482956 m1A Human chr16 + 58734260 58734260 58734260 TGGTGGACCGTAGGAGGGCAGTGGGCAGCCGCAGGACGGAGCAGAGGGCGAGCGGACACACACAC TGGTGGACCGTAGGAGGGCAGTGGGCAGCCGCCGGACGGAGCAGAGGGCGAGCGGACACACACAC A C AC106793.1 Ensembl:ENSG00000245768 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:58723826..58734325 26863196 MeRIP-seq:(Medium) rs774769517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1722341 95387 RMVar_ID_95387 Human_SNP_ID_604482970 m1A Human chr16 + 58734278 58734278 58734278 CAGTGGGCAGCCGCAGGACGGAGCAGAGGGCGAGCGGACACACACACAGGGAACCGGCTCCTGCT CAGTGGGCAGCCGCAGGACGGAGCAGAGGGCGTGCGGACACACACACAGGGAACCGGCTCCTGCT A T AC106793.1 Ensembl:ENSG00000245768 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:58734098..58749652;chr16:58734101..58734325 26863196 MeRIP-seq:(Medium) rs1445051111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1722341 95388 RMVar_ID_95388 Human_SNP_ID_135861473 m1A Human chr3 + 62322011 62322011 62322011 GATCAACACACAGAAAAGGCATCTCAACTCCAAACTGTTGAGACTGCTTTTAAAAGGAACCTTAG GATCAACACACAGAAAAGGCATCTCAACTCCAGACTGTTGAGACTGCTTTTAAAAGGAACCTTAG A G PTPRG-AS1 Ensembl:ENSG00000241472 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs763853296 Functional Loss SNV dbSNP153 33..33 33 - - - 95389 RMVar_ID_95389 Human_SNP_ID_135861474 m1A Human chr3 + 62322011 62322011 62322011 GATCAACACACAGAAAAGGCATCTCAACTCCAAACTGTTGAGACTGCTTTTAAAAGGAACCTTAG GATCAACACACAGAAAAGGCATCTCAACTCCATACTGTTGAGACTGCTTTTAAAAGGAACCTTAG A T PTPRG-AS1 Ensembl:ENSG00000241472 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs763853296 Functional Loss SNV dbSNP153 33..33 33 - - - 95390 RMVar_ID_95390 Human_SNP_ID_135874503 m1A Human chr3 - 62372554 62372521 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGG_________________________________ CCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCT C FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs1175181167 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95391 RMVar_ID_95391 Human_SNP_ID_135874521 m1A Human chr3 + 62372539 62372524 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCG_______________CCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG GCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs752755859 Functional Loss DEL dbSNP153 19..33 33 - - - 95392 RMVar_ID_95392 Human_SNP_ID_135874526 m1A Human chr3 + 62372539 62372527 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCG____________CCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG GCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs756214780 Functional Loss DEL dbSNP153 22..33 33 - - - 95393 RMVar_ID_95393 Human_SNP_ID_135874528 m1A Human chr3 - 62372554 62372527 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGG___________________________CGGCGG GCCGCCGCCGCCACCGCCGCCGCCGCCT G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs778332587 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95394 RMVar_ID_95394 Human_SNP_ID_135874532 m1A Human chr3 - 62372554 62372530 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGG________________________CGGCGGCGG GCCGCCGCCACCGCCGCCGCCGCCT G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs892646413 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95395 RMVar_ID_95395 Human_SNP_ID_135874534 m1A Human chr3 + 62372539 62372530 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCGCCG_________CCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG GCCGCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs749809403 Functional Loss DEL dbSNP153 25..33 33 - - - 95396 RMVar_ID_95396 Human_SNP_ID_135874539 m1A Human chr3 + 62372539 62372533 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCGCCGCCG______CCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG GCCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs746257480 Functional Loss DEL dbSNP153 28..33 33 - - - 95397 RMVar_ID_95397 Human_SNP_ID_135874541 m1A Human chr3 + 62372539 62372536 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCGCCGCCGCCG___CCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG GCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs771651427 Functional Loss DEL dbSNP153 31..33 33 - - - 95398 RMVar_ID_95398 Human_SNP_ID_135874551 m1A Human chr3 + 62372539 62372539 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs959459921 Functional Loss SNV dbSNP153 33..33 33 - - - 95399 RMVar_ID_95399 Human_SNP_ID_135874552 m1A Human chr3 + 62372539 62372539 62372539 CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG CACACTGGGGCCCCCCCGCCGCCGCCGCCGCCTCCGCCGCCGCCGCCTCCGCCGCCGCCCGCCCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr3:62372482..62372586;chr3:62372430..62372648 26863196 MeRIP-seq:(Medium) rs959459921 Functional Loss SNV dbSNP153 33..33 33 - - - 95400 RMVar_ID_95400 Human_SNP_ID_135874553 m1A Human chr3 - 62372554 62372542 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGG____________CGGTGGCGGCGGCGGCGGCGG GCCGCCGCCGCCT G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs765296597 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95401 RMVar_ID_95401 Human_SNP_ID_135874558 m1A Human chr3 - 62372554 62372545 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGG_________CGGCGGTGGCGGCGGCGGCGGCGG GCCGCCGCCT G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs750193151 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95402 RMVar_ID_95402 Human_SNP_ID_135874569 m1A Human chr3 - 62372554 62372554 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGTGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG T A FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs201688981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95403 RMVar_ID_95403 Human_SNP_ID_135874570 m1A Human chr3 - 62372554 62372554 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG T G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs201688981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5208191,Human_RBP_ID_18464653 95404 RMVar_ID_95404 Human_SNP_ID_136268371 m1A Human chr3 - 63835219 63835219 63835219 TGTATAAATTTTTTTCTTGTTAACACAGCTGGAATTGAGACGGAAACAGTTTCATGTTCTTCTTA TGTATAAATTTTTTTCTTGTTAACACAGCTGGTATTGAGACGGAAACAGTTTCATGTTCTTCTTA T A THOC7 Ensembl:ENSG00000163634 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:63835170..63836329 32194978 MeRIP-seq:(Medium) rs1158999129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_607225,Human_RBP_ID_1630950,Human_RBP_ID_7220043 Human_Splice_Rec_448720,Human_Splice_Rec_448721,Human_Splice_Rec_448732,Human_Splice_Rec_448733,Human_Splice_Rec_448746,Human_Splice_Rec_448756 Human_miRNA_ID_2647069,Human_miRNA_ID_2669662,Human_miRNA_ID_3100310 RMVar_hsa_circ_219386,RMVar_hsa_circ_219385,RMVar_hsa_circ_90217,RMVar_hsa_circ_219387,RMVar_hsa_circ_219389,RMVar_hsa_circ_94275,RMVar_hsa_circ_328494,RMVar_hsa_circ_219388 95405 RMVar_ID_95405 Human_SNP_ID_136275156 m1A Human chr3 + 63862814 63862814 63862814 TTCCCAGATATCAAAGGACCTCCTTCCTCCCTAACCAGATACCTTGTAGGTTCTCCCTCCAGTTG TTCCCAGATATCAAAGGACCTCCTTCCTCCCTGACCAGATACCTTGTAGGTTCTCCCTCCAGTTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:63862812..63863273 26863196 MeRIP-seq:(Medium) rs1220325062 Functional Loss SNV dbSNP153 33..33 33 - - - 95406 RMVar_ID_95406 Human_SNP_ID_136275405 m1A Human chr3 + 63863612 63863612 63863612 AGAGGAGGAAGGACTCAGGGAAGCAGCCGGGGAGGCCCGGGGCTCCGGGGAGAGGTCGGGAAGGC AGAGGAGGAAGGACTCAGGGAAGCAGCCGGGGTGGCCCGGGGCTCCGGGGAGAGGTCGGGAAGGC A T AC104162.2 Ensembl:ENSG00000285399 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:63863610..63863783 26863410 MeRIP-seq:(Medium) rs912316725 Functional Loss SNV dbSNP153 33..33 33 - - - 95407 RMVar_ID_95407 Human_SNP_ID_136275445 m1A Human chr3 + 63863707 63863707 63863707 CCGAGGGGTTCCCGGAAGCGGGCCGGGAGGCCAGGGGTCTCAGGGGAGGCCCAGCGGGCCGTGCA CCGAGGGGTTCCCGGAAGCGGGCCGGGAGGCCGGGGGTCTCAGGGGAGGCCCAGCGGGCCGTGCA A G AC104162.2 Ensembl:ENSG00000285399 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:63863704..63863850 26863196 MeRIP-seq:(Medium) rs935518680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5605358 95408 RMVar_ID_95408 Human_SNP_ID_136275446 m1A Human chr3 + 63863707 63863707 63863707 CCGAGGGGTTCCCGGAAGCGGGCCGGGAGGCCAGGGGTCTCAGGGGAGGCCCAGCGGGCCGTGCA CCGAGGGGTTCCCGGAAGCGGGCCGGGAGGCCTGGGGTCTCAGGGGAGGCCCAGCGGGCCGTGCA A T AC104162.2 Ensembl:ENSG00000285399 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:63863704..63863850 26863196 MeRIP-seq:(Medium) rs935518680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5605358 95409 RMVar_ID_95409 Human_SNP_ID_136275719 m1A Human chr3 + 63864220 63864220 63864220 CGGGGGTGCGGCGGGAGCTGCGGGCCGCCCGCAGTCGGGGTCCCGGCTTCTTCCCCGGGAAGGTG CGGGGGTGCGGCGGGAGCTGCGGGCCGCCCGCTGTCGGGGTCCCGGCTTCTTCCCCGGGAAGGTG A T AC104162.2,ATXN7 Ensembl:ENSG00000285399,Ensembl:ENSG00000163635 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:63864169..63864246 26863196 MeRIP-seq:(Medium) rs1373675986 Functional Loss SNV dbSNP153 33..33 33 - - - 95410 RMVar_ID_95410 Human_SNP_ID_136286269 m1A Human chr3 - 63906820 63906820 63906820 GCCTCCTGCAGGTAGTCTATGGTCTAGCCCAAATGACAAATTCAGAACTTCAAACATGCCCCCAC GCCTCCTGCAGGTAGTCTATGGTCTAGCCCAAGTGACAAATTCAGAACTTCAAACATGCCCCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:63906814..63906937 26863196 MeRIP-seq:(Medium) rs1487963929 Functional Loss SNV dbSNP153 33..33 33 - - - 95411 RMVar_ID_95411 Human_SNP_ID_136287592 m1A Human chr3 + 63912118 63912106 63912118 AGGGAGCCGGCCGGGTGCCGCCGCTCGGACGGACGCGCGGACGGAAGGAAGGAGCGGGGCAGCCG AGGGAGCCGGCCGGGTGCCGC____________CGCGCGGACGGAAGGAAGGAGCGGGGCAGCCG CCGCTCGGACGGA C ATXN7 Ensembl:ENSG00000163635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:63912074..63912200 26863196 MeRIP-seq:(Medium) rs1325408740 Functional Loss DEL dbSNP153 22..33 33 - - - Human_Splice_Rec_448909 RMVar_hsa_circ_32192,RMVar_hsa_circ_219391,RMVar_hsa_circ_77161,RMVar_hsa_circ_126772,RMVar_hsa_circ_219392,RMVar_hsa_circ_293554,RMVar_hsa_circ_304428,RMVar_hsa_circ_274923,RMVar_hsa_circ_219395,RMVar_hsa_circ_219396,RMVar_hsa_circ_219394 95412 RMVar_ID_95412 Human_SNP_ID_136291330 m1A Human chr3 + 63924335 63924335 63924335 TTCATGTGCGGCTGTGGTGTCAGCAGTTGAATACACAATCTGGAGCATGGTGGAGCAGTCTGGGG TTCATGTGCGGCTGTGGTGTCAGCAGTTGAATCCACAATCTGGAGCATGGTGGAGCAGTCTGGGG A C ATXN7 Ensembl:ENSG00000163635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:63924289..63924390 26863196 MeRIP-seq:(Medium) rs1431812886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32192,RMVar_hsa_circ_126772,RMVar_hsa_circ_219392,RMVar_hsa_circ_304428,RMVar_hsa_circ_274923,RMVar_hsa_circ_219397,RMVar_hsa_circ_219395,RMVar_hsa_circ_219396,RMVar_hsa_circ_296523,RMVar_hsa_circ_378351 95413 RMVar_ID_95413 Human_SNP_ID_136291448 m1A Human chr3 - 63924780 63924780 63924780 TTCAAAGTGAAACCCTTTAAAAAGCTGTCCATACTTGCCCTCTCCACTTCTTCAGCTCAGGCTAT TTCAAAGTGAAACCCTTTAAAAAGCTGTCCATTCTTGCCCTCTCCACTTCTTCAGCTCAGGCTAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:63924772..63925032 26863196 MeRIP-seq:(Medium) rs531868639 Functional Loss SNV dbSNP153 33..33 33 - - - 95414 RMVar_ID_95414 Human_SNP_ID_136318749 m1A Human chr3 - 64022493 64022493 64022493 AGACATGGCTCCTTACTATGAAGCCTTGTGCAAATCCCTCGACTGGCAGATAGACGTGGACCTAC AGACATGGCTCCTTACTATGAAGCCTTGTGCATATCCCTCGACTGGCAGATAGACGTGGACCTAC T A PSMD6 Ensembl:ENSG00000163636 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:64022301..64022525 32194978 MeRIP-seq:(Medium) rs369805299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393813,Human_RBP_ID_14926727,Human_RBP_ID_24547277 Human_Splice_Rec_448992,Human_Splice_Rec_449006,Human_Splice_Rec_449048,Human_Splice_Rec_449062,Human_Splice_Rec_449080,Human_Splice_Rec_449090,Human_Splice_Rec_449098 RMVar_hsa_circ_53870,RMVar_hsa_circ_219402,RMVar_hsa_circ_283010,RMVar_hsa_circ_360418 95415 RMVar_ID_95415 Human_SNP_ID_136318750 m1A Human chr3 - 64022493 64022493 64022493 AGACATGGCTCCTTACTATGAAGCCTTGTGCAAATCCCTCGACTGGCAGATAGACGTGGACCTAC AGACATGGCTCCTTACTATGAAGCCTTGTGCAGATCCCTCGACTGGCAGATAGACGTGGACCTAC T C PSMD6 Ensembl:ENSG00000163636 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:64022301..64022525 32194978 MeRIP-seq:(Medium) rs369805299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393813,Human_RBP_ID_14926727,Human_RBP_ID_24547277 Human_Splice_Rec_448992,Human_Splice_Rec_449006,Human_Splice_Rec_449048,Human_Splice_Rec_449062,Human_Splice_Rec_449080,Human_Splice_Rec_449090,Human_Splice_Rec_449098 RMVar_hsa_circ_53870,RMVar_hsa_circ_219402,RMVar_hsa_circ_283010,RMVar_hsa_circ_360418 95416 RMVar_ID_95416 Human_SNP_ID_136318751 m1A Human chr3 - 64022493 64022493 64022493 AGACATGGCTCCTTACTATGAAGCCTTGTGCAAATCCCTCGACTGGCAGATAGACGTGGACCTAC AGACATGGCTCCTTACTATGAAGCCTTGTGCACATCCCTCGACTGGCAGATAGACGTGGACCTAC T G PSMD6 Ensembl:ENSG00000163636 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:64022301..64022525 32194978 MeRIP-seq:(Medium) rs369805299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393813,Human_RBP_ID_14926727,Human_RBP_ID_24547277 Human_Splice_Rec_448992,Human_Splice_Rec_449006,Human_Splice_Rec_449048,Human_Splice_Rec_449062,Human_Splice_Rec_449080,Human_Splice_Rec_449090,Human_Splice_Rec_449098 RMVar_hsa_circ_53870,RMVar_hsa_circ_219402,RMVar_hsa_circ_283010,RMVar_hsa_circ_360418 95417 RMVar_ID_95417 Human_SNP_ID_136319129 m1A Human chr3 - 64023358 64023358 64023358 TCTGCCCAAGAACCCCGACTTGCGTATCGCGCAGCTGCGCTTCCTGCTCAGCCTGCCCGAGCACC TCTGCCCAAGAACCCCGACTTGCGTATCGCGCTGCTGCGCTTCCTGCTCAGCCTGCCCGAGCACC T A PSMD6 Ensembl:ENSG00000163636 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:64023237..64023450 26863196 MeRIP-seq:(Medium) rs1275915447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158279,Human_RBP_ID_9333776,Human_RBP_ID_9393814,Human_RBP_ID_22091790,Human_RBP_ID_23026743,Human_RBP_ID_26347031,Human_RBP_ID_27058613 Human_Splice_Rec_448991,Human_Splice_Rec_449045,Human_Splice_Rec_449095 95418 RMVar_ID_95418 Human_SNP_ID_136319169 m1A Human chr3 - 64023441 64023441 64023441 CGCAGCCGGTCGTAACCAAGTTGTGTCCTGTCAGCCGCTGTCCCCTTCGCCGCGATGCCGCTGGA CGCAGCCGGTCGTAACCAAGTTGTGTCCTGTCTGCCGCTGTCCCCTTCGCCGCGATGCCGCTGGA T A PSMD6 Ensembl:ENSG00000163636 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:64023325..64023475 26863196 MeRIP-seq:(Medium) rs143451892 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_158279,Human_RBP_ID_9333777,Human_RBP_ID_9393815,Human_RBP_ID_14926762,Human_RBP_ID_22091791,Human_RBP_ID_23026743,Human_RBP_ID_24016319,Human_RBP_ID_26347031 Human_Splice_Rec_449061,Human_Splice_Rec_449087 95419 RMVar_ID_95419 Human_SNP_ID_136685070 m1A Human chr3 - 65361160 65361160 65361160 CAAACTATGAAAACATTCCTTCCTTCCCTGGCATGACTCCATGAATTTGTCTCCAGAACGGCAGC CAAACTATGAAAACATTCCTTCCTTCCCTGGCGTGACTCCATGAATTTGTCTCCAGAACGGCAGC T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:65361157..65361300 26863196 MeRIP-seq:(Medium) rs1174175808 Functional Loss SNV dbSNP153 33..33 33 - - - 95420 RMVar_ID_95420 Human_SNP_ID_136698060 m1A Human chr3 - 65412055 65412055 65412055 TTTAATTGAAATGGTTTTGGGAAGCCATAGGGACATGGAGCCAGGAGACAGTACAATCTGATTTC TTTAATTGAAATGGTTTTGGGAAGCCATAGGGGCATGGAGCCAGGAGACAGTACAATCTGATTTC T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:65412053..65412179 26863196 MeRIP-seq:(Medium) rs561825531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61563,RMVar_hsa_circ_49641,RMVar_hsa_circ_219436,RMVar_hsa_circ_109831,RMVar_hsa_circ_219437,RMVar_hsa_circ_1154,RMVar_hsa_circ_25770,RMVar_hsa_circ_58902,RMVar_hsa_circ_265101,RMVar_hsa_circ_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058 95421 RMVar_ID_95421 Human_SNP_ID_136698080 m1A Human chr3 - 65412146 65412145 65412147 GGCTGGAGTGTGTGTCCAGGAGGAGGAAGTAAAGAGATAGGAGGGGTCACATCCAGGAGGGCTTA GGCTGGAGTGTGTGTCCAGGAGGAGGAAGTA__GAGATAGGAGGGGTCACATCCAGGAGGGCTTA CTT C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:65412144..65412224 26863196 MeRIP-seq:(Medium) rs1295401528 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_61563,RMVar_hsa_circ_49641,RMVar_hsa_circ_219436,RMVar_hsa_circ_109831,RMVar_hsa_circ_219437,RMVar_hsa_circ_1154,RMVar_hsa_circ_25770,RMVar_hsa_circ_58902,RMVar_hsa_circ_265101,RMVar_hsa_circ_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058 95422 RMVar_ID_95422 Human_SNP_ID_136699761 m1A Human chr3 - 65418531 65418531 65418531 GGGGAAGAAGATGGGATGCAACATAGGTGAGAAGGGGTAGGCCTTGGGGTTAGTCTGTGTAAACT GGGGAAGAAGATGGGATGCAACATAGGTGAGAGGGGGTAGGCCTTGGGGTTAGTCTGTGTAAACT T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:65418526..65418928 26863196 MeRIP-seq:(Medium) rs1356862798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11096,Human_RBP_ID_26790754 RMVar_hsa_circ_61563,RMVar_hsa_circ_49641,RMVar_hsa_circ_219436,RMVar_hsa_circ_109831,RMVar_hsa_circ_219437,RMVar_hsa_circ_1154,RMVar_hsa_circ_25770,RMVar_hsa_circ_58902,RMVar_hsa_circ_265101,RMVar_hsa_circ_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058 95423 RMVar_ID_95423 Human_SNP_ID_136745361 m1A Human chr3 - 65581659 65581659 65581659 GTAGGGCTTAATTAGGAATGTGATGTTTGTGCAAGAGATAGAGTGGAGAGTATTAACTTCACAAA GTAGGGCTTAATTAGGAATGTGATGTTTGTGCGAGAGATAGAGTGGAGAGTATTAACTTCACAAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:65581658..65581801 26863196 MeRIP-seq:(Medium) rs956126899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350792,RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_70633,RMVar_hsa_circ_61252,RMVar_hsa_circ_350933,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454,RMVar_hsa_circ_354891,RMVar_hsa_circ_60627,RMVar_hsa_circ_350450,RMVar_hsa_circ_219461,RMVar_hsa_circ_298028,RMVar_hsa_circ_359165 95424 RMVar_ID_95424 Human_SNP_ID_136870461 m1A Human chr3 - 66038130 66038130 66038130 GGTCGAGGCAGCGGGGCTTCCCGGCGGCGGCGAGGGCCCGAGGCTGGGCGAAGGGGAGCTGCTTC GGTCGAGGCAGCGGGGCTTCCCGGCGGCGGCGTGGGCCCGAGGCTGGGCGAAGGGGAGCTGCTTC T A MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:66038028..66038434 26863196 MeRIP-seq:(Medium) rs775737376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19012739,Human_RBP_ID_23026745 RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 95425 RMVar_ID_95425 Human_SNP_ID_136923650 m1A Human chr3 - 66236479 66236479 66236479 AAAAAAGGTTACAACAAAATAAGCTCTCGGCCACTTGGGGGCGAAGATAGGAAGACAGTCTTTAA AAAAAAGGTTACAACAAAATAAGCTCTCGGCCTCTTGGGGGCGAAGATAGGAAGACAGTCTTTAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:66236478..66236608 26863196 MeRIP-seq:(Medium) rs956885058 Functional Loss SNV dbSNP153 33..33 33 - - - 95426 RMVar_ID_95426 Human_SNP_ID_137001227 m1A Human chr3 - 66500593 66500593 66500593 GCGGGGTTTGCGGCCCCCGCCGGGTGCTCCGGAGCGGCCCGGGCACCGGGGGCACGCTGAGTGCC GCGGGGTTTGCGGCCCCCGCCGGGTGCTCCGGGGCGGCCCGGGCACCGGGGGCACGCTGAGTGCC T C LRIG1 Ensembl:ENSG00000144749 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:66500542..66500649 26863196 MeRIP-seq:(Medium) rs1269853148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756588,Human_RBP_ID_18464655,Human_RBP_ID_18471707,Human_RBP_ID_22456053 95427 RMVar_ID_95427 Human_SNP_ID_137001364 m1A Human chr3 - 66500910 66500910 66500910 GCGCGCGCGCGCTCTCTGGCCGCGGCGTGGGGACAGCGAGGCGCACTGGGGCCTCCCAGCGCGGG GCGCGCGCGCGCTCTCTGGCCGCGGCGTGGGGGCAGCGAGGCGCACTGGGGCCTCCCAGCGCGGG T C LRIG1 Ensembl:ENSG00000144749 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:66500862..66501004 26863196 MeRIP-seq:(Medium) rs574457727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784481,Human_RBP_ID_4756591,Human_RBP_ID_18424010,Human_RBP_ID_22456054 95428 RMVar_ID_95428 Human_SNP_ID_137001414 m1A Human chr3 - 66500957 66500957 66500957 CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGAACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGTACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG T A LRIG1 Ensembl:ENSG00000144749 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:66500852..66501021 26863196 MeRIP-seq:(Medium) rs372795968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756592,Human_RBP_ID_18424010 95429 RMVar_ID_95429 Human_SNP_ID_137001415 m1A Human chr3 - 66500957 66500957 66500957 CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGAACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGCACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG T G LRIG1 Ensembl:ENSG00000144749 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:66500852..66501021 26863196 MeRIP-seq:(Medium) rs372795968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756592,Human_RBP_ID_18424010 95430 RMVar_ID_95430 Human_SNP_ID_137276337 m1A Human chr3 - 67520525 67520525 67520525 CGTGCTGGTGGGCAGCCCCCAGGGGGGCGTCGACATTGAAGAGGTGGCTGCTTCAAACCCGGAGC CGTGCTGGTGGGCAGCCCCCAGGGGGGCGTCGCCATTGAAGAGGTGGCTGCTTCAAACCCGGAGC T G SUCLG2 Ensembl:ENSG00000172340 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:67520476..67520525 32194978 MeRIP-seq:(Medium) rs781757897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115890 Human_Splice_Rec_450423,Human_Splice_Rec_450437,Human_Splice_Rec_450451,Human_Splice_Rec_450471 RMVar_hsa_circ_358861,RMVar_hsa_circ_367299,RMVar_hsa_circ_96448,RMVar_hsa_circ_219507,RMVar_hsa_circ_219506,RMVar_hsa_circ_313854,RMVar_hsa_circ_342476,RMVar_hsa_circ_290961,RMVar_hsa_circ_219509,RMVar_hsa_circ_219510,RMVar_hsa_circ_219508,RMVar_hsa_circ_219517,RMVar_hsa_circ_62138,RMVar_hsa_circ_219515,RMVar_hsa_circ_111099,RMVar_hsa_circ_317887,RMVar_hsa_circ_353461,RMVar_hsa_circ_282783,RMVar_hsa_circ_219516,RMVar_hsa_circ_295309,RMVar_hsa_circ_219518,RMVar_hsa_circ_63538 95431 RMVar_ID_95431 Human_SNP_ID_137282839 m1A Human chr3 - 67545776 67545776 67545776 AATTAAATAACTTGGAAGTATTGCAGGGAAGCAGGTGGGAAAAGGAAGAATGAAAAGGAGAGAGG AATTAAATAACTTGGAAGTATTGCAGGGAAGCTGGTGGGAAAAGGAAGAATGAAAAGGAGAGAGG T A SUCLG2 Ensembl:ENSG00000172340 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:67545756..67545885 26863196 MeRIP-seq:(Medium) rs956420093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367299,RMVar_hsa_circ_219507,RMVar_hsa_circ_342476,RMVar_hsa_circ_219508,RMVar_hsa_circ_353461,RMVar_hsa_circ_282783,RMVar_hsa_circ_219518,RMVar_hsa_circ_358757,RMVar_hsa_circ_219520 95432 RMVar_ID_95432 Human_SNP_ID_137311078 m1A Human chr3 - 67654555 67654555 67654555 GATGGCGTCCCCCGTAGCAGCGCAGGCCGGGAAGCTTCTGCGAGCCCTAGCGCTGCGGCCCCGCT GATGGCGTCCCCCGTAGCAGCGCAGGCCGGGAGGCTTCTGCGAGCCCTAGCGCTGCGGCCCCGCT T C SUCLG2 Ensembl:ENSG00000172340 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:67609526..67654639;chr3:67654460..67654842;chr3:67654465..67654564;chr3:67654478..67654587 26863196 MeRIP-seq:(Medium) rs912703262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424011,Human_RBP_ID_22457386,Human_RBP_ID_24017835 Human_Splice_Rec_450415,Human_Splice_Rec_450443,Human_Splice_Rec_450463 95433 RMVar_ID_95433 Human_SNP_ID_137311184 m1A Human chr3 - 67654737 67654737 67654737 AAGAACGCCTGTGCCCCCGGGACGCAGGGGTCAGGCCCGGCCCGGCCCAGACCGCCTCTGCCTCC AAGAACGCCTGTGCCCCCGGGACGCAGGGGTCTGGCCCGGCCCGGCCCAGACCGCCTCTGCCTCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:67654696..67654861 26863196 MeRIP-seq:(Medium) rs1278224094 Functional Loss SNV dbSNP153 33..33 33 - - - 95434 RMVar_ID_95434 Human_SNP_ID_137570320 m1A Human chr3 + 68635765 68635765 68635765 GTCCTGGAGGTGGCAAGAAGGATGACAAGGACAAGAAAAAGAAATATGAACCTCCTGTACCAACT GTCCTGGAGGTGGCAAGAAGGATGACAAGGACGAGAAAAAGAAATATGAACCTCCTGTACCAACT A G PSMC1P1 Ensembl:ENSG00000241506 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:68635716..68635866 26863196 MeRIP-seq:(Medium) rs1252136333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5101978,Human_RBP_ID_7237575,Human_RBP_ID_8264853,Human_RBP_ID_17405875 Human_miRNA_ID_1844336 95435 RMVar_ID_95435 Human_SNP_ID_137674009 m1A Human chr3 - 69013575 69013575 69013575 CCTCCTCGGTAGTTCACGGCTGCCCCGGCTCCAGGTGGGACTCCCCCGCAATCTGCGGAGCCTTC CCTCCTCGGTAGTTCACGGCTGCCCCGGCTCCGGGTGGGACTCCCCCGCAATCTGCGGAGCCTTC T C EOGT Ensembl:ENSG00000163378 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:69013535..69013686 26863196 MeRIP-seq:(Medium) rs1177428739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19117985 Human_Splice_Rec_450631,Human_Splice_Rec_450659,Human_Splice_Rec_450709,Human_Splice_Rec_450791,Human_Splice_Rec_450801 95436 RMVar_ID_95436 Human_SNP_ID_137676240 m1A Human chr3 + 69021642 69021642 69021642 TTCAAGATGGTGTACTTGTATCTATATTCTGAAGTACTAGTGTTTTAATTTTAACTAAAAATTAA TTCAAGATGGTGTACTTGTATCTATATTCTGAGGTACTAGTGTTTTAATTTTAACTAAAAATTAA A G AC109587.1 Ensembl:ENSG00000244513 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:69021575..69021676 32194978 MeRIP-seq:(Medium) rs1423898909 Functional Loss SNV dbSNP153 33..33 33 - - - 95437 RMVar_ID_95437 Human_SNP_ID_137690955 m1A Human chr3 - 69077917 69077917 69077917 TTTGCAGCTGAATTTACTGTGTTCTGTGCAGAATGGCTGTTGATGGTGGGTGTGGGGACACTGGA TTTGCAGCTGAATTTACTGTGTTCTGTGCAGATTGGCTGTTGATGGTGGGTGTGGGGACACTGGA T A UBA3 Ensembl:ENSG00000144744 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:69077801..69079783;chr3:69077771..69077964;chr3:69077776..69079783 26863196 MeRIP-seq:(Medium) rs1165899409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933243,Human_RBP_ID_3965380,Human_RBP_ID_4753033,Human_RBP_ID_9348871,Human_RBP_ID_18424013,Human_RBP_ID_19010707,Human_RBP_ID_22552215,Human_RBP_ID_26346309,Human_RBP_ID_27823361 Human_Splice_Rec_450996,Human_Splice_Rec_451028,Human_Splice_Rec_451058,Human_Splice_Rec_451090,Human_Splice_Rec_451114,Human_Splice_Rec_451150,Human_Splice_Rec_451162,Human_Splice_Rec_451168,Human_Splice_Rec_451174,Human_Splice_Rec_451180 RMVar_hsa_circ_1785,RMVar_hsa_circ_19230,RMVar_hsa_circ_2701,RMVar_hsa_circ_324803,RMVar_hsa_circ_320703,RMVar_hsa_circ_334644,RMVar_hsa_circ_333046 95438 RMVar_ID_95438 Human_SNP_ID_137690956 m1A Human chr3 - 69077917 69077917 69077917 TTTGCAGCTGAATTTACTGTGTTCTGTGCAGAATGGCTGTTGATGGTGGGTGTGGGGACACTGGA TTTGCAGCTGAATTTACTGTGTTCTGTGCAGAGTGGCTGTTGATGGTGGGTGTGGGGACACTGGA T C UBA3 Ensembl:ENSG00000144744 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:69077801..69079783;chr3:69077771..69077964;chr3:69077776..69079783 26863196 MeRIP-seq:(Medium) rs1165899409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933243,Human_RBP_ID_3965380,Human_RBP_ID_4753033,Human_RBP_ID_9348871,Human_RBP_ID_18424013,Human_RBP_ID_19010707,Human_RBP_ID_22552215,Human_RBP_ID_26346309,Human_RBP_ID_27823361 Human_Splice_Rec_450996,Human_Splice_Rec_451028,Human_Splice_Rec_451058,Human_Splice_Rec_451090,Human_Splice_Rec_451114,Human_Splice_Rec_451150,Human_Splice_Rec_451162,Human_Splice_Rec_451168,Human_Splice_Rec_451174,Human_Splice_Rec_451180 RMVar_hsa_circ_1785,RMVar_hsa_circ_19230,RMVar_hsa_circ_2701,RMVar_hsa_circ_324803,RMVar_hsa_circ_320703,RMVar_hsa_circ_334644,RMVar_hsa_circ_333046 95439 RMVar_ID_95439 Human_SNP_ID_137691614 m1A Human chr3 + 69080273 69080273 69080273 GTGGGGACCCCGGGTGGCGGCGGCAACCGCCCACCGCCGCGCTCTCTCACAACCCAGCCCAGCCC GTGGGGACCCCGGGTGGCGGCGGCAACCGCCCGCCGCCGCGCTCTCTCACAACCCAGCCCAGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:69080272..69080375 26863196 MeRIP-seq:(Medium) rs1037650036 Functional Loss SNV dbSNP153 33..33 33 - - - 95440 RMVar_ID_95440 Human_SNP_ID_137691617 m1A Human chr3 - 69080283 69080283 69080283 CAGACGCGCCGGGCTGGGCTGGGTTGTGAGAGAGCGCGGCGGTGGGCGGTTGCCGCCGCCACCCG CAGACGCGCCGGGCTGGGCTGGGTTGTGAGAGGGCGCGGCGGTGGGCGGTTGCCGCCGCCACCCG T C UBA3 Ensembl:ENSG00000144744 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:69080281..69080375 26863196 MeRIP-seq:(Medium) rs368483921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19115899 95441 RMVar_ID_95441 Human_SNP_ID_137692779 m1A Human chr3 + 69085043 69085043 69085043 GCCAGATTCTGGAGGCGAAGAACGCAAAGCTGAGAACATGGACGTTAATATCGCCCCACTCCGCG GCCAGATTCTGGAGGCGAAGAACGCAAAGCTGCGAACATGGACGTTAATATCGCCCCACTCCGCG A C ARL6IP5 Ensembl:ENSG00000144746 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:69084992..69085112 26863196 MeRIP-seq:(Medium) rs1325998210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1631177 RMVar_hsa_circ_123032,RMVar_hsa_circ_219562 95442 RMVar_ID_95442 Human_SNP_ID_137692790 m1A Human chr3 - 69085061 69085061 69085061 GGAAGAAATCGTCCCAGGCGCGGAGTGGGGCGATATTAACGTCCATGTTCTCAGCTTTGCGTTCT GGAAGAAATCGTCCCAGGCGCGGAGTGGGGCGGTATTAACGTCCATGTTCTCAGCTTTGCGTTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:69084956..69085175;chr3:69084986..69085147;chr3:69084964..69085110 26863196 MeRIP-seq:(Medium) rs1383054019 Functional Loss SNV dbSNP153 33..33 33 - - - 95443 RMVar_ID_95443 Human_SNP_ID_137870306 m1A Human chr3 - 69739556 69739556 69739556 TTCCCGTCCTTCCACTGCTGGAAAGTGAGAACAGAGCCCGGGGGCGGAGGGAAGGTAGCTGGGCC TTCCCGTCCTTCCACTGCTGGAAAGTGAGAACGGAGCCCGGGGGCGGAGGGAAGGTAGCTGGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:69739507..69739655 26863196 MeRIP-seq:(Medium) rs1454691300 Functional Loss SNV dbSNP153 33..33 33 - - - 95444 RMVar_ID_95444 Human_SNP_ID_137870339 m1A Human chr3 + 69739641 69739641 69739641 ATCGGGGATCGTGCCGGATTTCGAAGTCGGGGAGGAGTTTCATGAAGAGCCCAAAACCTATTACG ATCGGGGATCGTGCCGGATTTCGAAGTCGGGGGGGAGTTTCATGAAGAGCCCAAAACCTATTACG A G MITF Ensembl:ENSG00000187098 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:69739508..69739720 26863196 MeRIP-seq:(Medium) rs758114521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23026525 Human_Splice_Rec_451431,Human_Splice_Rec_451449,Human_Splice_Rec_451451,Human_Splice_Rec_451455,Human_Splice_Rec_451473 95445 RMVar_ID_95445 Human_SNP_ID_137879410 m1A Human chr3 - 69778105 69778105 69778105 TTACCACTTAAGTCCAACGAATCACCCACCCTACGATTCTCCTTCCCTGATATCTCTCAGCTCCA TTACCACTTAAGTCCAACGAATCACCCACCCTGCGATTCTCCTTCCCTGATATCTCTCAGCTCCA T C lnc-FRMD4B-4 RNACentral:URS00008C14AA lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:69778016..69778145 26863196 MeRIP-seq:(Medium) rs1349613906 Functional Loss SNV dbSNP153 33..33 33 - - - 95446 RMVar_ID_95446 Human_SNP_ID_138270376 m1A Human chr3 - 71290105 71290105 71290105 CCAGGAATGTAGTTGTAGATATGGGAGGTTTGAGCTATGCACCCAGACTAAGATGCCAAGTGGGC CCAGGAATGTAGTTGTAGATATGGGAGGTTTGGGCTATGCACCCAGACTAAGATGCCAAGTGGGC T C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:71290095..71290298 26863196 MeRIP-seq:(Medium) rs1024061687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8236197,Human_RBP_ID_22418375,Human_RBP_ID_24383336 RMVar_hsa_circ_82550,RMVar_hsa_circ_219594,RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_70236,RMVar_hsa_circ_316285,RMVar_hsa_circ_54457,RMVar_hsa_circ_64045,RMVar_hsa_circ_304923,RMVar_hsa_circ_333764,RMVar_hsa_circ_336895,RMVar_hsa_circ_286827,RMVar_hsa_circ_315358,RMVar_hsa_circ_219615,RMVar_hsa_circ_277933 95447 RMVar_ID_95447 Human_SNP_ID_138270568 m1A Human chr3 - 71290944 71290944 71290944 AAAGAGAGCAAGTCAGCCAGTATGGCCGAAGCAGTGTCCTTAAGGGAAGAGTACAGGTTGAGTAT AAAGAGAGCAAGTCAGCCAGTATGGCCGAAGCGGTGTCCTTAAGGGAAGAGTACAGGTTGAGTAT T C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:71290938..71291137 26863196 MeRIP-seq:(Medium) rs1305508586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82550,RMVar_hsa_circ_219594,RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_70236,RMVar_hsa_circ_316285,RMVar_hsa_circ_54457,RMVar_hsa_circ_64045,RMVar_hsa_circ_304923,RMVar_hsa_circ_333764,RMVar_hsa_circ_336895,RMVar_hsa_circ_286827,RMVar_hsa_circ_315358,RMVar_hsa_circ_219615,RMVar_hsa_circ_277933 95448 RMVar_ID_95448 Human_SNP_ID_138278002 m1A Human chr3 + 71319830 71319830 71319830 CTACAACCTTCTTCAGCACCCTCTTCTCCGCCAATCTGGTTCTTCTTCCTTGGGCCTTCCCTCAG CTACAACCTTCTTCAGCACCCTCTTCTCCGCCTATCTGGTTCTTCTTCCTTGGGCCTTCCCTCAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:71319801..71320017 26863196 MeRIP-seq:(Medium) rs1209075915 Functional Loss SNV dbSNP153 33..33 33 - - - 95449 RMVar_ID_95449 Human_SNP_ID_138278047 m1A Human chr3 + 71319993 71319993 71319993 TTTCCTTCACCCTGACCAACACTTGCCGGCCCACACAAGGGTGCCTCCCACGACTCTGCAATTCC TTTCCTTCACCCTGACCAACACTTGCCGGCCCTCACAAGGGTGCCTCCCACGACTCTGCAATTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:71319964..71320089 26863196 MeRIP-seq:(Medium) rs1351204357 Functional Loss SNV dbSNP153 33..33 33 - - - 95450 RMVar_ID_95450 Human_SNP_ID_138278150 m1A Human chr3 - 71320405 71320404 71320405 ATCTGTGCAGCGGCTTAGAGACAAGACTGTACAGGGTGTGTATGTGAGTGTCTGTCCGTGGTAGA ATCTGTGCAGCGGCTTAGAGACAAGACTGTAC_GGGTGTGTATGTGAGTGTCTGTCCGTGGTAGA CT C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:71320399..71320513 26863196 MeRIP-seq:(Medium) rs1429931170 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82550,RMVar_hsa_circ_219594,RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_316285,RMVar_hsa_circ_54457,RMVar_hsa_circ_64045,RMVar_hsa_circ_219617,RMVar_hsa_circ_304923,RMVar_hsa_circ_333764,RMVar_hsa_circ_286827,RMVar_hsa_circ_315358,RMVar_hsa_circ_219615,RMVar_hsa_circ_277768,RMVar_hsa_circ_343399,RMVar_hsa_circ_116417,RMVar_hsa_circ_219618 95451 RMVar_ID_95451 Human_SNP_ID_138345931 m1A Human chr3 - 71582394 71582394 71582394 GCGAGCCGAGGCGGCGTGCGCTTCGAGTGGGGACCACGGCGGTGGCGGCGGCGCCGGGAGCCGAG GCGAGCCGAGGCGGCGTGCGCTTCGAGTGGGGTCCACGGCGGTGGCGGCGGCGCCGGGAGCCGAG T A AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71582391..71582547 26863196 MeRIP-seq:(Medium) rs966513655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_219617,RMVar_hsa_circ_116417 95452 RMVar_ID_95452 Human_SNP_ID_138345979 m1A Human chr3 + 71582500 71582500 71582500 AGGGAGCTCGGGAGGAAGGCTGCGCGCAAGCGAGGGACGGAGAGCCATCGGCCGCCAGGACAGGG AGGGAGCTCGGGAGGAAGGCTGCGCGCAAGCGGGGGACGGAGAGCCATCGGCCGCCAGGACAGGG A G AC097634.3 Ensembl:ENSG00000277855 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:71582310..71582752;chr3:71581430..71583939;chr3:71582365..71582742 26863196 MeRIP-seq:(Medium) rs1458432106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5605318,Human_RBP_ID_26790768 95453 RMVar_ID_95453 Human_SNP_ID_138388187 m1A Human chr3 + 71753671 71753647 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCC________________________GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG CGCGGCGGCGGCGGCGGCGGCGGCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1393158576 Functional Loss DEL dbSNP153 10..33 33 - - - 95454 RMVar_ID_95454 Human_SNP_ID_138388204 m1A Human chr3 + 71753671 71753650 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCG_____________________GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGCGGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1376632163 Functional Loss DEL dbSNP153 13..33 33 - - - 95455 RMVar_ID_95455 Human_SNP_ID_138388209 m1A Human chr3 + 71753671 71753653 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCGGCG__________________GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1197876494 Functional Loss DEL dbSNP153 16..33 33 - - - 95456 RMVar_ID_95456 Human_SNP_ID_138388227 m1A Human chr3 + 71753671 71753665 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCGGCGGCGGCGGCGGCG______GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1177979032 Functional Loss DEL dbSNP153 28..33 33 - - - 95457 RMVar_ID_95457 Human_SNP_ID_138388230 m1A Human chr3 + 71753671 71753668 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCGGCGGCGGCGGCGGCGGCG___GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1207768184 Functional Loss DEL dbSNP153 31..33 33 - - - 95458 RMVar_ID_95458 Human_SNP_ID_138388233 m1A Human chr3 + 71753671 71753670 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGC_GCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs1302090026 Functional Loss DEL dbSNP153 33..33 33 - - - 95459 RMVar_ID_95459 Human_SNP_ID_138388234 m1A Human chr3 + 71753671 71753671 71753671 GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG GGGGGCTCCGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGGCCCGGCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:71753649..71753724 26863196 MeRIP-seq:(Medium) rs548598109 Functional Loss SNV dbSNP153 33..33 33 - - - 95460 RMVar_ID_95460 Human_SNP_ID_138388501 m1A Human chr3 + 71754198 71754198 71754198 CGCGCTGCTGATCGTGCGGGAGCGCAGCCTGCACCGCGCCCCGTACTACCTGCTGCTCGACCTGT CGCGCTGCTGATCGTGCGGGAGCGCAGCCTGCGCCGCGCCCCGTACTACCTGCTGCTCGACCTGT A G GPR27 Ensembl:ENSG00000170837 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:71754099..71754200 26863410 MeRIP-seq:(Medium) rs751505827 Functional Loss SNV dbSNP153 33..33 33 - - - 95461 RMVar_ID_95461 Human_SNP_ID_138544135 m1A Human chr3 - 72379320 72379320 72379320 GGAGAAGAAGGAGAAAGTTGAAAAGCAGGACAAAGAGAAACCTGAGAAAGACAAGGAAATTAGTC GGAGAAGAAGGAGAAAGTTGAAAAGCAGGACAGAGAGAAACCTGAGAAAGACAAGGAAATTAGTC T C RYBP Ensembl:ENSG00000163602 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:72379271..72379370 26863196 MeRIP-seq:(Medium) rs748543491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14937455 Human_Splice_Rec_453793 95462 RMVar_ID_95462 Human_SNP_ID_138562452 m1A Human chr3 + 72446744 72446744 72446744 GCCGTCGTAATTTCGCAGGAATCCAGTGCTGGAAACTTCGCTCGGGAGACCACCCACCCACCCTT GCCGTCGTAATTTCGCAGGAATCCAGTGCTGGCAACTTCGCTCGGGAGACCACCCACCCACCCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:72446704..72446849 26863196 MeRIP-seq:(Medium) rs1415592152 Functional Loss SNV dbSNP153 33..33 33 - - - 95463 RMVar_ID_95463 Human_SNP_ID_138647796 m1A Human chr3 - 72787826 72787826 72787826 CCTGCAATCCCAGGCACTTGGCAGGCTGAGGCAGGAGAATCAGGCAGGGAGGTTGCAGTGAGTCG CCTGCAATCCCAGGCACTTGGCAGGCTGAGGCGGGAGAATCAGGCAGGGAGGTTGCAGTGAGTCG T C SHQ1 Ensembl:ENSG00000144736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:72787821..72787901 26863196 MeRIP-seq:(Medium) rs981938295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88183,RMVar_hsa_circ_105141,RMVar_hsa_circ_219641,RMVar_hsa_circ_219642,RMVar_hsa_circ_219643 95464 RMVar_ID_95464 Human_SNP_ID_138663033 m1A Human chr3 + 72848379 72848379 72848379 ACCGGACGCAAGGGCCGGCGCCGCTCGCTCTCACTGCCGCCGCGTTCCCGCCACGCAAACTCTCC ACCGGACGCAAGGGCCGGCGCCGCTCGCTCTCCCTGCCGCCGCGTTCCCGCCACGCAAACTCTCC A C lnc-GXYLT2-1 RNACentral:URS00008C05EB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:72848308..72848397 26863196 MeRIP-seq:(Medium) rs1187095200 Functional Loss SNV dbSNP153 33..33 33 - - - 95465 RMVar_ID_95465 Human_SNP_ID_138663034 m1A Human chr3 + 72848379 72848379 72848379 ACCGGACGCAAGGGCCGGCGCCGCTCGCTCTCACTGCCGCCGCGTTCCCGCCACGCAAACTCTCC ACCGGACGCAAGGGCCGGCGCCGCTCGCTCTCGCTGCCGCCGCGTTCCCGCCACGCAAACTCTCC A G lnc-GXYLT2-1 RNACentral:URS00008C05EB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:72848308..72848397 26863196 MeRIP-seq:(Medium) rs1187095200 Functional Loss SNV dbSNP153 33..33 33 - - - 95466 RMVar_ID_95466 Human_SNP_ID_138663056 m1A Human chr3 - 72848407 72848407 72848407 CACCGAGAGTTCCTGCGCGTGGGGAGTTGGAGAGTTTGCGTGGCGGGAACGCGGCGGCAGTGAGA CACCGAGAGTTCCTGCGCGTGGGGAGTTGGAGCGTTTGCGTGGCGGGAACGCGGCGGCAGTGAGA T G SHQ1 Ensembl:ENSG00000144736 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:72848303..72848414 26863196 MeRIP-seq:(Medium) rs1270442799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24019412 RMVar_hsa_circ_99257,RMVar_hsa_circ_219660 95467 RMVar_ID_95467 Human_SNP_ID_138663061 m1A Human chr3 - 72848415 72848415 72848415 GTCCCTCACACCGAGAGTTCCTGCGCGTGGGGAGTTGGAGAGTTTGCGTGGCGGGAACGCGGCGG GTCCCTCACACCGAGAGTTCCTGCGCGTGGGGGGTTGGAGAGTTTGCGTGGCGGGAACGCGGCGG T C SHQ1 Ensembl:ENSG00000144736 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:72848237..72848432 26863196 MeRIP-seq:(Medium) rs1462293905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4753452 RMVar_hsa_circ_99257,RMVar_hsa_circ_219660 95468 RMVar_ID_95468 Human_SNP_ID_139120359 m1A Human chr3 + 74614465 74614435 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCG______________________________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs1021296509 Functional Loss DEL dbSNP153 4..33 33 - - - 95469 RMVar_ID_95469 Human_SNP_ID_139120361 m1A Human chr3 + 74614465 74614438 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCG___________________________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs1383896580 Functional Loss DEL dbSNP153 7..33 33 - - - 95470 RMVar_ID_95470 Human_SNP_ID_139120367 m1A Human chr3 + 74614465 74614441 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCG________________________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs1445810955 Functional Loss DEL dbSNP153 10..33 33 - - - 95471 RMVar_ID_95471 Human_SNP_ID_139120371 m1A Human chr3 + 74614465 74614444 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCG_____________________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs1315937076 Functional Loss DEL dbSNP153 13..33 33 - - - 95472 RMVar_ID_95472 Human_SNP_ID_139120374 m1A Human chr3 + 74614465 74614447 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCG__________________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs965559725 Functional Loss DEL dbSNP153 16..33 33 - - - 95473 RMVar_ID_95473 Human_SNP_ID_139120379 m1A Human chr3 + 74614465 74614450 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCG_______________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs975611022 Functional Loss DEL dbSNP153 19..33 33 - - - 95474 RMVar_ID_95474 Human_SNP_ID_139120384 m1A Human chr3 + 74614465 74614453 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCG____________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs921675789 Functional Loss DEL dbSNP153 22..33 33 - - - 95475 RMVar_ID_95475 Human_SNP_ID_139120388 m1A Human chr3 + 74614465 74614456 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCG_________CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs1182061946 Functional Loss DEL dbSNP153 25..33 33 - - - 95476 RMVar_ID_95476 Human_SNP_ID_139120393 m1A Human chr3 + 74614465 74614459 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCGCCG______CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCGCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs953109908 Functional Loss DEL dbSNP153 28..33 33 - - - 95477 RMVar_ID_95477 Human_SNP_ID_139120397 m1A Human chr3 + 74614465 74614462 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCG___CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs746683819 Functional Loss DEL dbSNP153 31..33 33 - - - 95478 RMVar_ID_95478 Human_SNP_ID_139120400 m1A Human chr3 + 74614465 74614465 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG A C lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs540003516 Functional Loss SNV dbSNP153 33..33 33 - - - 95479 RMVar_ID_95479 Human_SNP_ID_139120401 m1A Human chr3 + 74614465 74614465 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG A G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs540003516 Functional Loss SNV dbSNP153 33..33 33 - - - 95480 RMVar_ID_95480 Human_SNP_ID_690704018 m1A Human chr21 - 22034828 22034819 22034828 AGAAGAAGAAGAAAAAGAAGAAGAGGAAGAAGAGGAAGAAGCAGAAGAAAAGAAGAAGAAGAAGG AGAAGAAGAAGAAAAAGAAGAAGAGGAAGAAG_________CAGAAGAAAAGAAGAAGAAGAAGG GCTTCTTCCT G LINC01687 Ensembl:ENSG00000233215 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:22034709..22034830 26863196 MeRIP-seq:(Medium) rs1406163095 Functional Loss DEL dbSNP153 33..41 33 - - - 95481 RMVar_ID_95481 Human_SNP_ID_691599184 m1A Human chr21 + 25362417 25362417 25362417 TTGACAAATACACAGAGGTCCTCAAGACCCACAGACTCCTGGTCTGAGCCCAATAAAGACTGTTA TTGACAAATACACAGAGGTCCTCAAGACCCACGGACTCCTGGTCTGAGCCCAATAAAGACTGTTA A G RPL13AP7 Ensembl:ENSG00000213885 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1023836361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1902685 95482 RMVar_ID_95482 Human_SNP_ID_691601765 m1A Human chr21 + 25373662 25373650 25373662 CTCCTCTCCCCACCCCTCCTCCTCCTCCTCCCACTCCTCCCCCTTCTCCTCCCCCTCCCTTCCTC CTCCTCTCCCCACCCCTCCTC____________CTCCTCCCCCTTCTCCTCCCCCTCCCTTCCTC CCTCCTCCTCCCA C RPL13AP7 Ensembl:ENSG00000213885 Pseudogene intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:25373612..25373739 26863196 MeRIP-seq:(Medium) rs1229376823 Functional Loss DEL dbSNP153 22..33 33 - - - 95483 RMVar_ID_95483 Human_SNP_ID_691601770 m1A Human chr21 + 25373662 25373662 25373662 CTCCTCTCCCCACCCCTCCTCCTCCTCCTCCCACTCCTCCCCCTTCTCCTCCCCCTCCCTTCCTC CTCCTCTCCCCACCCCTCCTCCTCCTCCTCCCCCTCCTCCCCCTTCTCCTCCCCCTCCCTTCCTC A C RPL13AP7 Ensembl:ENSG00000213885 Pseudogene intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:25373612..25373739 26863196 MeRIP-seq:(Medium) rs1343248208 Functional Loss SNV dbSNP153 33..33 33 - - - 95484 RMVar_ID_95484 Human_SNP_ID_691654614 m1A Human chr21 + 25607444 25607444 25607444 TCCCGCCACCGGGTGCGACCAGCCAGAGCCGCAGCGCCCGGGAACCCATGGCCAGCGCCTCCATA TCCCGCCACCGGGTGCGACCAGCCAGAGCCGCTGCGCCCGGGAACCCATGGCCAGCGCCTCCATA A T lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:25607345..25607457;chr21:25607341..25607449 26863196 MeRIP-seq:(Medium) rs755816400 Functional Loss SNV dbSNP153 33..33 33 - - - 95485 RMVar_ID_95485 Human_SNP_ID_691654630 m1A Human chr21 + 25607454 25607453 25607455 GGGTGCGACCAGCCAGAGCCGCAGCGCCCGGGAACCCATGGCCAGCGCCTCCATAGCAGCGGTGA GGGTGCGACCAGCCAGAGCCGCAGCGCCCGGG__CCCATGGCCAGCGCCTCCATAGCAGCGGTGA GAA G lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:25607395..25607468 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 33..34 33 - - - 95486 RMVar_ID_95486 Human_SNP_ID_691672213 m1A Human chr21 + 25683938 25683938 25683938 GCCCCAAAAGACCAACAAGTAGTCACAGCAGTAGAGTACCAAGGTACAGTATCTTACTGATTTTC GCCCCAAAAGACCAACAAGTAGTCACAGCAGTGGAGTACCAAGGTACAGTATCTTACTGATTTTC A G JAM2 Ensembl:ENSG00000154721 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8133602 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_2112338,Human_Splice_Rec_2112339,Human_Splice_Rec_2112356,Human_Splice_Rec_2112357,Human_Splice_Rec_2112374,Human_Splice_Rec_2112375 RMVar_hsa_circ_306192,RMVar_hsa_circ_344362 95487 RMVar_ID_95487 Human_SNP_ID_691680409 m1A Human chr21 + 25718710 25718708 25718710 GCGCTTCTCTGTCACACTTTCCTTTCACCCCCAGTTATCTCTGGCCCCTCATCGCCTTCCTGGTC GCGCTTCTCTGTCACACTTTCCTTTCACCCC__GTTATCTCTGGCCCCTCATCGCCTTCCTGGTC CCA C lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:25718659..25718817 26863196 MeRIP-seq:(Medium) rs917464406 Functional Loss DEL dbSNP153 32..33 33 - - - 95488 RMVar_ID_95488 Human_SNP_ID_691680505 m1A Human chr21 + 25719109 25719109 25719109 CCACCCTCCAGTACCCTCTCAGTCACAACGTCAATCTCTCCAGTTCCAAAGGCTCCTTTTCCCTC CCACCCTCCAGTACCCTCTCAGTCACAACGTCCATCTCTCCAGTTCCAAAGGCTCCTTTTCCCTC A C lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:25718986..25719138 26863196 MeRIP-seq:(Medium) rs901774469 Functional Loss SNV dbSNP153 33..33 33 - - - 95489 RMVar_ID_95489 Human_SNP_ID_691680533 m1A Human chr21 - 25719187 25719187 25719187 GGGAAAGGAGAAGGGAGTTGACATGGTTCGAGAGAAATGGGGCAAATTGATGGATGGGGTGGGGG GGGAAAGGAGAAGGGAGTTGACATGGTTCGAGGGAAATGGGGCAAATTGATGGATGGGGTGGGGG T C ATP5PF Ensembl:ENSG00000154723 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:25718998..25719296 26863196 MeRIP-seq:(Medium) rs1450395925 Functional Loss SNV dbSNP153 33..33 33 - - - 95490 RMVar_ID_95490 Human_SNP_ID_691683003 m1A Human chr21 - 25729797 25729797 25729797 CGTTTCTGCTGCTTGTTTTCTGTAACAGAATCAGCATGATTCTTCAGAGGCTCTTCAGGTTCTCC CGTTTCTGCTGCTTGTTTTCTGTAACAGAATCGGCATGATTCTTCAGAGGCTCTTCAGGTTCTCC T C ATP5PF Ensembl:ENSG00000154723 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:25729713..25729832 26863196 MeRIP-seq:(Medium) rs1343418699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679853,Human_RBP_ID_5148617,Human_RBP_ID_5323676,Human_RBP_ID_9332080,Human_RBP_ID_18423580,Human_RBP_ID_24534344 Human_Splice_Rec_2112418,Human_Splice_Rec_2112428,Human_Splice_Rec_2112434,Human_Splice_Rec_2112440,Human_Splice_Rec_2112446,Human_Splice_Rec_2112452,Human_Splice_Rec_2112458,Human_Splice_Rec_2112464 95491 RMVar_ID_95491 Human_SNP_ID_691684443 m1A Human chr21 + 25734869 25734869 25734869 CTACCCTCCCAGTCACCTTGCACTCAGTCCCGAGCTGCCAAAGCCTCCGCCGCCACCACCTCCGC CTACCCTCCCAGTCACCTTGCACTCAGTCCCGGGCTGCCAAAGCCTCCGCCGCCACCACCTCCGC A G GABPA Ensembl:ENSG00000154727 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:25729686..25735181 26863196 MeRIP-seq:(Medium) rs1340898190 Functional Loss SNV dbSNP153 33..33 33 - - - 95492 RMVar_ID_95492 Human_SNP_ID_691684776 m1A Human chr21 - 25735617 25735617 25735617 GGGAAAAGGCCCCGGAACGAGGCCGGCCCGCGAGGGCCCGCGCTCCCCTCCTCCCCGGCGGCCGC GGGAAAAGGCCCCGGAACGAGGCCGGCCCGCGCGGGCCCGCGCTCCCCTCCTCCCCGGCGGCCGC T G ATP5PF Ensembl:ENSG00000154723 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:25735526..25741624 26863410 MeRIP-seq:(Medium) rs1025251538 Functional Loss SNV dbSNP153 33..33 33 - - - 95493 RMVar_ID_95493 Human_SNP_ID_691750254 m1A Human chr21 + 25955723 25955723 25955723 GTGTGCTGTCTGTCCTTCTGTTCTGCGCGGACATACTTCTTTAGCATATTGAACACGTGACGAGG GTGTGCTGTCTGTCCTTCTGTTCTGCGCGGACGTACTTCTTTAGCATATTGAACACGTGACGAGG A G lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:25955673..25955798 26863196 MeRIP-seq:(Medium) rs755218930 Functional Loss SNV dbSNP153 33..33 33 - - - 95494 RMVar_ID_95494 Human_SNP_ID_691755533 m1A Human chr21 - 25976005 25976005 25976005 AATTTATAGGTCATGAGAGAATGGGAAGAGGCAGAACGTCAAGCAAAGAACTTGCCTAAAGCTGA AATTTATAGGTCATGAGAGAATGGGAAGAGGCGGAACGTCAAGCAAAGAACTTGCCTAAAGCTGA T C APP Ensembl:ENSG00000142192 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:25975900..25976078;chr21:25975951..25976050 26863196 MeRIP-seq:(Medium) rs556540232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63808,Human_RBP_ID_1602154,Human_RBP_ID_1934290,Human_RBP_ID_4666808,Human_RBP_ID_5597103,Human_RBP_ID_7032168,Human_RBP_ID_9391329,Human_RBP_ID_14213594,Human_RBP_ID_17670956,Human_RBP_ID_17701129,Human_RBP_ID_22453957,Human_RBP_ID_22507150,Human_RBP_ID_22767916 Human_Splice_Rec_2112520,Human_Splice_Rec_2112521,Human_Splice_Rec_2112550,Human_Splice_Rec_2112551,Human_Splice_Rec_2112584,Human_Splice_Rec_2112585,Human_Splice_Rec_2112616,Human_Splice_Rec_2112617,Human_Splice_Rec_2112646,Human_Splice_Rec_2112647,Human_Splice_Rec_2112678,Human_Splice_Rec_2112679,Human_Splice_Rec_2112710,Human_Splice_Rec_2112711,Human_Splice_Rec_2112748,Human_Splice_Rec_2112749,Human_Splice_Rec_2112774,Human_Splice_Rec_2112775,Human_Splice_Rec_2112790,Human_Splice_Rec_2112791 RMVar_hsa_circ_4256,RMVar_hsa_circ_53034,RMVar_hsa_circ_30326,RMVar_hsa_circ_72605,RMVar_hsa_circ_31488,RMVar_hsa_circ_20814,RMVar_hsa_circ_27786,RMVar_hsa_circ_57207,RMVar_hsa_circ_296357,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_295921,RMVar_hsa_circ_276290,RMVar_hsa_circ_287350,RMVar_hsa_circ_289014,RMVar_hsa_circ_324079,RMVar_hsa_circ_301007,RMVar_hsa_circ_344865,RMVar_hsa_circ_332936,RMVar_hsa_circ_300003,RMVar_hsa_circ_59446,RMVar_hsa_circ_273506,RMVar_hsa_circ_211612,RMVar_hsa_circ_211613 95495 RMVar_ID_95495 Human_SNP_ID_691761700 m1A Human chr21 - 26000006 26000006 26000006 GCATGGCCGTGTGTGGCAGCGCCAGTAAGTGGACCCTTCTTCGAGCCTGGCCACCTTTCGTCTCT GCATGGCCGTGTGTGGCAGCGCCAGTAAGTGGTCCCTTCTTCGAGCCTGGCCACCTTTCGTCTCT T A APP Ensembl:ENSG00000142192 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:26000001..26000050 32194978 MeRIP-seq:(Medium) rs754403217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30326,RMVar_hsa_circ_72605,RMVar_hsa_circ_31488,RMVar_hsa_circ_20814,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_276290,RMVar_hsa_circ_289014,RMVar_hsa_circ_344865,RMVar_hsa_circ_332936,RMVar_hsa_circ_59446,RMVar_hsa_circ_35844,RMVar_hsa_circ_37023,RMVar_hsa_circ_43543,RMVar_hsa_circ_57301 95496 RMVar_ID_95496 Human_SNP_ID_691761782 m1A Human chr21 - 26000182 26000182 26000182 TAAATGTGGTTCCCCACATCTCCTCTGATTAGAGGTGTGCTCTGAACAAGCCGAGACGGGGCCGT TAAATGTGGTTCCCCACATCTCCTCTGATTAGTGGTGTGCTCTGAACAAGCCGAGACGGGGCCGT T A APP Ensembl:ENSG00000142192 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:26000151..26000200 26863196 MeRIP-seq:(Medium) rs1227000828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1934305,Human_RBP_ID_9391332,Human_RBP_ID_27300572 Human_Splice_Rec_2112578,Human_Splice_Rec_2112612,Human_Splice_Rec_2112674,Human_Splice_Rec_2112704,Human_Splice_Rec_2112742,Human_Splice_Rec_2112770,Human_Splice_Rec_2112796 RMVar_hsa_circ_30326,RMVar_hsa_circ_72605,RMVar_hsa_circ_31488,RMVar_hsa_circ_20814,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_276290,RMVar_hsa_circ_289014,RMVar_hsa_circ_344865,RMVar_hsa_circ_332936,RMVar_hsa_circ_59446,RMVar_hsa_circ_35844,RMVar_hsa_circ_37023,RMVar_hsa_circ_43543,RMVar_hsa_circ_57301,RMVar_hsa_circ_73432 95497 RMVar_ID_95497 Human_SNP_ID_691767762 m1A Human chr21 + 26021995 26021995 26021995 CGTCCTCGTCATCATCGGCTTCTTCTTCTTCCACCTCAGCCACTTCTTCCTCCTCTGCTACTTCT CGTCCTCGTCATCATCGGCTTCTTCTTCTTCCCCCTCAGCCACTTCTTCCTCCTCTGCTACTTCT A C lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:26021818..26022075 26863196 MeRIP-seq:(Medium) rs201093867 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12587,GWAS_ID_12588 95498 RMVar_ID_95498 Human_SNP_ID_691775189 m1A Human chr21 + 26051005 26051005 26051005 TGAGGCTGAACACAAAGGCCACCTTACCTCCCATCTGCATAGTCTGTGTCTGCTCCGCCCCACCA TGAGGCTGAACACAAAGGCCACCTTACCTCCCGTCTGCATAGTCTGTGTCTGCTCCGCCCCACCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:26051001..26051075 32194978 MeRIP-seq:(Medium) rs1266813363 Functional Loss SNV dbSNP153 33..33 33 - - - 95499 RMVar_ID_95499 Human_SNP_ID_691775195 m1A Human chr21 + 26051013 26051013 26051013 AACACAAAGGCCACCTTACCTCCCATCTGCATAGTCTGTGTCTGCTCCGCCCCACCAGACATCCG AACACAAAGGCCACCTTACCTCCCATCTGCATTGTCTGTGTCTGCTCCGCCCCACCAGACATCCG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:26051001..26051025 26863196 MeRIP-seq:(Medium) rs1217362785 Functional Loss SNV dbSNP153 33..33 33 - - - 95500 RMVar_ID_95500 Human_SNP_ID_691775244 m1A Human chr21 - 26051175 26051175 26051175 CTTACACTTTGTAGACATGCAGTGAGAAGAGTACCAACTTGCATGACTACGGCATGTTGCTGCCC CTTACACTTTGTAGACATGCAGTGAGAAGAGTTCCAACTTGCATGACTACGGCATGTTGCTGCCC T A APP Ensembl:ENSG00000142192 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:26051126..26051175 32194978 MeRIP-seq:(Medium) rs749504313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570254,Human_RBP_ID_1602181,Human_RBP_ID_1934339,Human_RBP_ID_23921351 Human_Splice_Rec_2112514,Human_Splice_Rec_2112544,Human_Splice_Rec_2112574,Human_Splice_Rec_2112608,Human_Splice_Rec_2112640,Human_Splice_Rec_2112670,Human_Splice_Rec_2112700,Human_Splice_Rec_2112738,Human_Splice_Rec_2112766,Human_Splice_Rec_2112806,Human_Splice_Rec_2112812,Human_Splice_Rec_2112818 RMVar_hsa_circ_72605,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_344865,RMVar_hsa_circ_332936,RMVar_hsa_circ_59446,RMVar_hsa_circ_37023,RMVar_hsa_circ_73432,RMVar_hsa_circ_317846,RMVar_hsa_circ_298430,RMVar_hsa_circ_211616,RMVar_hsa_circ_280131,RMVar_hsa_circ_342533,RMVar_hsa_circ_328636,RMVar_hsa_circ_268457 95501 RMVar_ID_95501 Human_SNP_ID_691784926 m1A Human chr21 - 26090054 26090049 26090055 GTGTGCTCTCCCAGGTCTACCCTGAACTGCAGATCACCAATGTGGTAGAAGCCAACCAACCAGTG GTGTGCTCTCCCAGGTCTACCCTGAACTGCA______CAATGTGGTAGAAGCCAACCAACCAGTG GGTGATC G APP Ensembl:ENSG00000142192 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:26090003..26090130 26863196 MeRIP-seq:(Medium) rs781218975 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_928539,Human_RBP_ID_1602194,Human_RBP_ID_1934353,Human_RBP_ID_5597112,Human_RBP_ID_9391341,Human_RBP_ID_14216161,Human_RBP_ID_18471319,Human_RBP_ID_18778509,Human_RBP_ID_22454089,Human_RBP_ID_27300576,Human_RBP_ID_27489302 Human_Splice_Rec_2112510,Human_Splice_Rec_2112540,Human_Splice_Rec_2112570,Human_Splice_Rec_2112604,Human_Splice_Rec_2112636,Human_Splice_Rec_2112666,Human_Splice_Rec_2112696,Human_Splice_Rec_2112734,Human_Splice_Rec_2112802,Human_Splice_Rec_2112820 RMVar_hsa_circ_72605,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_344865,RMVar_hsa_circ_59446,RMVar_hsa_circ_37023,RMVar_hsa_circ_298430,RMVar_hsa_circ_342533,RMVar_hsa_circ_328636,RMVar_hsa_circ_211617,RMVar_hsa_circ_310832,RMVar_hsa_circ_376378 95502 RMVar_ID_95502 Human_SNP_ID_691786671 m1A Human chr21 - 26097124 26097124 26097124 TCATGTGGTGGGAATTAGTGAACTAGCATGCAAGCCGGGCCTTTTTCTTGGCTTTTGTTCAATTG TCATGTGGTGGGAATTAGTGAACTAGCATGCAGGCCGGGCCTTTTTCTTGGCTTTTGTTCAATTG T C APP Ensembl:ENSG00000142192 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:26097122..26097260 26863196 MeRIP-seq:(Medium) rs1230990168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7032650 RMVar_hsa_circ_329745,RMVar_hsa_circ_344865,RMVar_hsa_circ_37023,RMVar_hsa_circ_298430,RMVar_hsa_circ_342533,RMVar_hsa_circ_310832 95503 RMVar_ID_95503 Human_SNP_ID_691798760 m1A Human chr21 - 26145130 26145130 26145130 AGTCAGCCAGCTTTTGATAGTTCTCCCCAGAGACTTCATCCCACAGGCAAGCCATCCCATTCCAC AGTCAGCCAGCTTTTGATAGTTCTCCCCAGAGGCTTCATCCCACAGGCAAGCCATCCCATTCCAC T C APP Ensembl:ENSG00000142192 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:26145125..26145270 26863196 MeRIP-seq:(Medium) rs377391806 Functional Loss SNV dbSNP153 33..33 33 - - - 95504 RMVar_ID_95504 Human_SNP_ID_691805408 m1A Human chr21 - 26170666 26170666 26170666 GTGGCGGCGCGGGCAGAGCAAGGACGCGGCGGATCCCACTCGCACAGCAGCGCACTCGGTGCCCC GTGGCGGCGCGGGCAGAGCAAGGACGCGGCGGGTCCCACTCGCACAGCAGCGCACTCGGTGCCCC T C APP Ensembl:ENSG00000142192 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:26170551..26170785 26863196 MeRIP-seq:(Medium) rs1457987504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63837,Human_RBP_ID_245071,Human_RBP_ID_570282,Human_RBP_ID_780163,Human_RBP_ID_928543,Human_RBP_ID_1602246,Human_RBP_ID_4666860,Human_RBP_ID_7033099,Human_RBP_ID_9391346,Human_RBP_ID_14218612,Human_RBP_ID_18778550,Human_RBP_ID_27025738,Human_RBP_ID_27489309 95505 RMVar_ID_95505 Human_SNP_ID_691968597 m1A Human chr21 - 26837076 26837076 26837076 AGGATCTTTGACCAGCACTGTTTATGGCTGCTATGGTTTCAGAGAATGTTTATACATTATTTCTA AGGATCTTTGACCAGCACTGTTTATGGCTGCTGTGGTTTCAGAGAATGTTTATACATTATTTCTA T C ADAMTS1 Ensembl:ENSG00000154734 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4666898,Human_RBP_ID_22507155,Human_RBP_ID_26494487 Human_miRNA_ID_1318636,Human_miRNA_ID_1320218 GWAS_ID_12589,GWAS_ID_12590 95506 RMVar_ID_95506 Human_SNP_ID_691970857 m1A Human chr21 - 26844320 26844318 26844321 GGACGACGAGCCCCGGCCGACTGGGAAAGCGGAGACCGAAGACGAGGACGAAGGGACTGAGGGCG GGACGACGAGCCCCGGCCGACTGGGAAAGCG___ACCGAAGACGAGGACGAAGGGACTGAGGGCG TCTC T ADAMTS1 Ensembl:ENSG00000154734 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:26844271..26844360 26863196 MeRIP-seq:(Medium) rs753850405 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_2112905 95507 RMVar_ID_95507 Human_SNP_ID_692000782 m1A Human chr21 + 26966524 26966521 26966524 TTGCTTGCAGGATTGAGTCAAGTGTCGGAGGGAGGGGGGCCCGGCAGCAGCGCCAGCCTGTCCGG TTGCTTGCAGGATTGAGTCAAGTGTCGGAG___GGGGGGCCCGGCAGCAGCGCCAGCCTGTCCGG GGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:26966478..26966567 26863196 MeRIP-seq:(Medium) rs892758310 Functional Loss DEL dbSNP153 31..33 33 - - - 95508 RMVar_ID_95508 Human_SNP_ID_692001131 m1A Human chr21 - 26967530 26967530 26967530 GGGGAAAAACTTGCGGCAGGAACTTCCCACCGAGGGCGAGAAAAGCAGGCAAGAAGGAGGCAGGG GGGGAAAAACTTGCGGCAGGAACTTCCCACCGTGGGCGAGAAAAGCAGGCAAGAAGGAGGCAGGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:26967484..26967732 26863196 MeRIP-seq:(Medium) rs1236361978 Functional Loss SNV dbSNP153 33..33 33 - - - 95509 RMVar_ID_95509 Human_SNP_ID_692496608 m1A Human chr21 - 28960866 28960866 28960866 GAAGTGAACATCATACAGGCTTAATGGGGAACAGGGAGGATACCAGTCTTCCTAGAACTTCAGGA GAAGTGAACATCATACAGGCTTAATGGGGAACCGGGAGGATACCAGTCTTCCTAGAACTTCAGGA T G LTN1 Ensembl:ENSG00000198862 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:28960822..28960893 26863196 MeRIP-seq:(Medium) rs1402427856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9432050,Human_RBP_ID_14220843,Human_RBP_ID_22507165 RMVar_hsa_circ_952,RMVar_hsa_circ_47791,RMVar_hsa_circ_86161,RMVar_hsa_circ_211631,RMVar_hsa_circ_324558,RMVar_hsa_circ_352389,RMVar_hsa_circ_211637,RMVar_hsa_circ_12444,RMVar_hsa_circ_344473,RMVar_hsa_circ_18904,RMVar_hsa_circ_25074,RMVar_hsa_circ_92714,RMVar_hsa_circ_17634,RMVar_hsa_circ_32547,RMVar_hsa_circ_3316,RMVar_hsa_circ_211643,RMVar_hsa_circ_211642 95510 RMVar_ID_95510 Human_SNP_ID_692506050 m1A Human chr21 + 28999467 28999467 28999467 TATTAATACTTAAATTTTCCCAATTTCACCCCACTCTTGGGTCACAATCTCTCTTGCCAGATTCC TATTAATACTTAAATTTTCCCAATTTCACCCCCCTCTTGGGTCACAATCTCTCTTGCCAGATTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:28999423..28999541 26863196 MeRIP-seq:(Medium) rs1432217242 Functional Loss SNV dbSNP153 33..33 33 - - - 95511 RMVar_ID_95511 Human_SNP_ID_692512106 m1A Human chr21 - 29019290 29019290 29019290 TAAGTTTTGGGTCGCAGTATGCTAGAATTTTGAGGCTCCCTTCTGATGAAAATTGAGCTGTCCAT TAAGTTTTGGGTCGCAGTATGCTAGAATTTTGGGGCTCCCTTCTGATGAAAATTGAGCTGTCCAT T C RWDD2B Ensembl:ENSG00000156253 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:29019239..29019317 26863196 MeRIP-seq:(Medium) rs1289023712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570422,Human_RBP_ID_1602348,Human_RBP_ID_4679858,Human_RBP_ID_14222220,Human_RBP_ID_18423344 Human_Splice_Rec_2113395,Human_Splice_Rec_2113403,Human_Splice_Rec_2113413,Human_Splice_Rec_2113419,Human_Splice_Rec_2113425,Human_Splice_Rec_2113427,Human_Splice_Rec_2113431 RMVar_hsa_circ_211649,RMVar_hsa_circ_77994 95512 RMVar_ID_95512 Human_SNP_ID_692513655 m1A Human chr21 + 29024743 29024743 29024743 AAGACGGAGCTGGCTGCCCAGCCCAAAGGCCCATGAGGGGATGCAGTTATGGGCTCTGTCGCCGT AAGACGGAGCTGGCTGCCCAGCCCAAAGGCCCGTGAGGGGATGCAGTTATGGGCTCTGTCGCCGT A G USP16 Ensembl:ENSG00000156256 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:29024694..29024841 26863196 MeRIP-seq:(Medium) rs1298296365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4667364,Human_RBP_ID_18423347 Human_Splice_Rec_2113439,Human_Splice_Rec_2113473,Human_Splice_Rec_2113509,Human_Splice_Rec_2113541,Human_Splice_Rec_2113549 95513 RMVar_ID_95513 Human_SNP_ID_692516577 m1A Human chr21 - 29036322 29036322 29036322 CTGGCTTGTTTTCTGACATAATCAACCACTTGACCCAACTGGTTTGAACTACAATACTGGACCTC CTGGCTTGTTTTCTGACATAATCAACCACTTGGCCCAACTGGTTTGAACTACAATACTGGACCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:29034847..29036328 32194978 MeRIP-seq:(Medium) rs1436443462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7034214 95514 RMVar_ID_95514 Human_SNP_ID_692520848 m1A Human chr21 + 29052657 29052655 29052658 ATCAGGAATGAAGCCAAAAGTCTTCATAGGTGAGGAGAATATGAGCATTGGAGATCCTGTTAGGT ATCAGGAATGAAGCCAAAAGTCTTCATAGGT___GAGAATATGAGCATTGGAGATCCTGTTAGGT TGAG T USP16 Ensembl:ENSG00000156256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:29052614..29052695;chr21:29052608..29052740 26863196 MeRIP-seq:(Medium) rs1233478786 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_14223767 RMVar_hsa_circ_362700,RMVar_hsa_circ_364878,RMVar_hsa_circ_339370,RMVar_hsa_circ_211652 95515 RMVar_ID_95515 Human_SNP_ID_692523185 m1A Human chr21 + 29060632 29060632 29060632 TTCCCAGGTAAGTATCTAGAATACCAGCTTCCAGCATGTCCTTTACAGCAGGGACTTCAGCCTGT TTCCCAGGTAAGTATCTAGAATACCAGCTTCCGGCATGTCCTTTACAGCAGGGACTTCAGCCTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:29060581..29060700 26863196 MeRIP-seq:(Medium) rs751712775 Functional Loss SNV dbSNP153 33..33 33 - - - 95516 RMVar_ID_95516 Human_SNP_ID_692523617 m1A Human chr21 - 29062131 29062131 29062131 GACGATGGTGTTAATACTTTCAAAGTTCTTACAAGGGTCAGTATCAGCAATATTCTTAGTAGTTT GACGATGGTGTTAATACTTTCAAAGTTCTTACGAGGGTCAGTATCAGCAATATTCTTAGTAGTTT T C CCT8 Ensembl:ENSG00000156261 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:29061384..29062250 32194978 MeRIP-seq:(Medium) rs1568910676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2699723,Human_RBP_ID_9391351,Human_RBP_ID_14224192,Human_RBP_ID_19110559 Human_Splice_Rec_2113607,Human_Splice_Rec_2113615,Human_Splice_Rec_2113641,Human_Splice_Rec_2113667,Human_Splice_Rec_2113695 RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,RMVar_hsa_circ_19543,RMVar_hsa_circ_211658,RMVar_hsa_circ_211660,RMVar_hsa_circ_211661,RMVar_hsa_circ_211662,RMVar_hsa_circ_211659,RMVar_hsa_circ_211656,RMVar_hsa_circ_211657,RMVar_hsa_circ_28303,RMVar_hsa_circ_48189,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_9343,RMVar_hsa_circ_88909,RMVar_hsa_circ_355486,RMVar_hsa_circ_356352,RMVar_hsa_circ_35494,RMVar_hsa_circ_36878,RMVar_hsa_circ_93831,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211665,RMVar_hsa_circ_211666 95517 RMVar_ID_95517 Human_SNP_ID_692523635 m1A Human chr21 - 29062178 29062178 29062178 TTCGAGGCTCTACAGACAATCTGATGGATGACATAGAAAGGGCAGTAGACGATGGTGTTAATACT TTCGAGGCTCTACAGACAATCTGATGGATGACGTAGAAAGGGCAGTAGACGATGGTGTTAATACT T C CCT8 Ensembl:ENSG00000156261 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:29062106..29062233 26863196 MeRIP-seq:(Medium) rs769948169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570484,Human_RBP_ID_1602435,Human_RBP_ID_1934695,Human_RBP_ID_7034488,Human_RBP_ID_8261326,Human_RBP_ID_14224192,Human_RBP_ID_17981390,Human_RBP_ID_23006518,Human_RBP_ID_23922172,Human_RBP_ID_27025932,Human_RBP_ID_27489372 Human_Splice_Rec_2113606,Human_Splice_Rec_2113607,Human_Splice_Rec_2113615,Human_Splice_Rec_2113640,Human_Splice_Rec_2113641,Human_Splice_Rec_2113666,Human_Splice_Rec_2113667,Human_Splice_Rec_2113694,Human_Splice_Rec_2113695,Human_Splice_Rec_2113706,Human_Splice_Rec_2113726 Human_miRNA_ID_3114784 RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,RMVar_hsa_circ_19543,RMVar_hsa_circ_211658,RMVar_hsa_circ_211660,RMVar_hsa_circ_211661,RMVar_hsa_circ_211662,RMVar_hsa_circ_211659,RMVar_hsa_circ_211656,RMVar_hsa_circ_211657,RMVar_hsa_circ_28303,RMVar_hsa_circ_48189,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_9343,RMVar_hsa_circ_88909,RMVar_hsa_circ_355486,RMVar_hsa_circ_356352,RMVar_hsa_circ_35494,RMVar_hsa_circ_36878,RMVar_hsa_circ_93831,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211665,RMVar_hsa_circ_211666 95518 RMVar_ID_95518 Human_SNP_ID_692525908 m1A Human chr21 + 29070334 29070334 29070334 GTTTCTATACACAGCCTCTTCTAATCCTGAAAAGTGCTGTTAAAAAAAACAAACAAAAAACCCCG GTTTCTATACACAGCCTCTTCTAATCCTGAAAGGTGCTGTTAAAAAAAACAAACAAAAAACCCCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:29070226..29070350 32194978 MeRIP-seq:(Medium) rs921733643 Functional Loss SNV dbSNP153 33..33 33 - - - 95519 RMVar_ID_95519 Human_SNP_ID_692526815 m1A Human chr21 + 29073602 29073602 29073602 CTTGGGAACGTGAAGCGCCATGGCCAGCCTGCAGGAAGCAGTTCACGCGACCGCTCGGAAGACCG CTTGGGAACGTGAAGCGCCATGGCCAGCCTGCCGGAAGCAGTTCACGCGACCGCTCGGAAGACCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:29073376..29073650 26863196 MeRIP-seq:(Medium) rs771369866 Functional Loss SNV dbSNP153 33..33 33 - - - 95520 RMVar_ID_95520 Human_SNP_ID_692577420 m1A Human chr21 - 29298955 29298955 29298955 GGAGAAGGGCCGGCGGGACGGCCGAGCCACTCACCAGAGCTGAGGCGCGGCGCGGCCCGACTGAC GGAGAAGGGCCGGCGGGACGGCCGAGCCACTCGCCAGAGCTGAGGCGCGGCGCGGCCCGACTGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr21:29298935..29299062;chr21:29298922..29299059;chr21:29298936..29299072 26863196 MeRIP-seq:(Medium) rs1379947967 Functional Loss SNV dbSNP153 33..33 33 - - - 95521 RMVar_ID_95521 Human_SNP_ID_692586710 m1A Human chr21 + 29336373 29336373 29336373 GTCCTTTATATTGTGTCGCCTAGGGAGGCAGGAGGTCCAGTGTCAGTATTGTCGTACCTGGGTAG GTCCTTTATATTGTGTCGCCTAGGGAGGCAGGCGGTCCAGTGTCAGTATTGTCGTACCTGGGTAG A C BACH1 Ensembl:ENSG00000156273 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:29336323..29336436 26863196 MeRIP-seq:(Medium) rs886640627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14225752,Human_RBP_ID_17145185 RMVar_hsa_circ_76256,RMVar_hsa_circ_111522,RMVar_hsa_circ_211679,RMVar_hsa_circ_352660,RMVar_hsa_circ_211685,RMVar_hsa_circ_287704,RMVar_hsa_circ_378831,RMVar_hsa_circ_211681,RMVar_hsa_circ_211686,RMVar_hsa_circ_278081,RMVar_hsa_circ_49157,RMVar_hsa_circ_211687,RMVar_hsa_circ_211691 95522 RMVar_ID_95522 Human_SNP_ID_692590956 m1A Human chr21 - 29354462 29354462 29354462 CTGGTCCAGTCCACCTAACTTCTTGTCTGACTACAGCCGTGGTTTCTTACTGGTATCTCCCATTC CTGGTCCAGTCCACCTAACTTCTTGTCTGACTCCAGCCGTGGTTTCTTACTGGTATCTCCCATTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:29354414..29354542 26863196 MeRIP-seq:(Medium) rs1217373856 Functional Loss SNV dbSNP153 33..33 33 - - - 95523 RMVar_ID_95523 Human_SNP_ID_692592187 m1A Human chr21 - 29358829 29358829 29358829 TTTTTTACTTCTTTCTATTTAGCACTTTTTACATTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT TTTTTTACTTCTTTCTATTTAGCACTTTTTACTTTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:29358794..29358913 26863196 MeRIP-seq:(Medium) rs766936334 Functional Loss SNV dbSNP153 33..33 33 - - - 95524 RMVar_ID_95524 Human_SNP_ID_692592188 m1A Human chr21 - 29358829 29358829 29358829 TTTTTTACTTCTTTCTATTTAGCACTTTTTACATTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT TTTTTTACTTCTTTCTATTTAGCACTTTTTACGTTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:29358794..29358913 26863196 MeRIP-seq:(Medium) rs766936334 Functional Loss SNV dbSNP153 33..33 33 - - - 95525 RMVar_ID_95525 Human_SNP_ID_692592189 m1A Human chr21 - 29358829 29358829 29358829 TTTTTTACTTCTTTCTATTTAGCACTTTTTACATTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT TTTTTTACTTCTTTCTATTTAGCACTTTTTACCTTTCTTTCTTTCTTCTTTCTTTCTTTCTTTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:29358794..29358913 26863196 MeRIP-seq:(Medium) rs766936334 Functional Loss SNV dbSNP153 33..33 33 - - - 95526 RMVar_ID_95526 Human_SNP_ID_692603200 m1A Human chr21 - 29407174 29407174 29407174 CTTCATACTTCATGATCCCCTTAAAAGCCCCCACCCAGGACTCCTCGGGGAGATGGATATGAGGG CTTCATACTTCATGATCCCCTTAAAAGCCCCCCCCCAGGACTCCTCGGGGAGATGGATATGAGGG T G lnc-GRIK1-3 RNACentral:URS00008BC4C4 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:29407132..29407219 26863196 MeRIP-seq:(Medium) rs1016978881 Functional Loss SNV dbSNP153 33..33 33 - - - 95527 RMVar_ID_95527 Human_SNP_ID_692620594 m1A Human chr21 + 29477891 29477891 29477891 ACAGAGGTGGGAATGGTGTGTCTAAGGAATGCAGGTTGGAGCACAGACAGCTAGAGGAAGAGAGC ACAGAGGTGGGAATGGTGTGTCTAAGGAATGCGGGTTGGAGCACAGACAGCTAGAGGAAGAGAGC A G BACH1 Ensembl:ENSG00000156273 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:29477772..29478006 26863196 MeRIP-seq:(Medium) rs992040453 Functional Loss SNV dbSNP153 33..33 33 - - - 95528 RMVar_ID_95528 Human_SNP_ID_692620767 m1A Human chr21 - 29478737 29478737 29478737 TTCCTCCCAAAGTTCCGTCCATTTTAGGTCCCACCTGTCTCTTGAATCTGGCCACTAGTCTCCAG TTCCTCCCAAAGTTCCGTCCATTTTAGGTCCCGCCTGTCTCTTGAATCTGGCCACTAGTCTCCAG T C lnc-GRIK1-3 RNACentral:URS00008BC4C4 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:29478643..29478837 26863196 MeRIP-seq:(Medium) rs1489273728 Functional Loss SNV dbSNP153 33..33 33 - - - 95529 RMVar_ID_95529 Human_SNP_ID_692822041 m1A Human chr21 - 30263639 30263639 30263639 AGCTGTGGTTGGTGTGGTGGCTGGAGGTGGCCAAATTGACAAACCCATCCTGAAGGCTGGCTGGG AGCTGTGGTTGGTGTGGTGGCTGGAGGTGGCCGAATTGACAAACCCATCCTGAAGGCTGGCTGGG T C RPL8P2 Ensembl:ENSG00000225267 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879119900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1136487,Human_RBP_ID_17398000 Human_miRNA_ID_1878515,Human_miRNA_ID_1897414 95530 RMVar_ID_95530 Human_SNP_ID_693170184 m1A Human chr21 - 31659727 31659726 31659727 GCCACGCCGAGGTCCTGGTTCCGAGGACTGCAACGGAAACCCCAGACGCTGCAGGAGACTACGAC GCCACGCCGAGGTCCTGGTTCCGAGGACTGCA_CGGAAACCCCAGACGCTGCAGGAGACTACGAC GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr21:31659626..31659888;chr21:31659676..31659853 26863196 MeRIP-seq:(Medium) rs1457550323 Functional Loss DEL dbSNP153 33..33 33 - - - 95531 RMVar_ID_95531 Human_SNP_ID_693170188 m1A Human chr21 - 31659727 31659727 31659727 GCCACGCCGAGGTCCTGGTTCCGAGGACTGCAACGGAAACCCCAGACGCTGCAGGAGACTACGAC GCCACGCCGAGGTCCTGGTTCCGAGGACTGCACCGGAAACCCCAGACGCTGCAGGAGACTACGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr21:31659626..31659888;chr21:31659676..31659853 26863196 MeRIP-seq:(Medium) rs902279948 Functional Loss SNV dbSNP153 33..33 33 - - - 95532 RMVar_ID_95532 Human_SNP_ID_693170189 m1A Human chr21 - 31659728 31659728 31659728 GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCAACGGAAACCCCAGACGCTGCAGGAGACTACGA GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCTACGGAAACCCCAGACGCTGCAGGAGACTACGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:31659651..31659900 26863196 MeRIP-seq:(Medium) rs755349211 Functional Loss SNV dbSNP153 33..33 33 - - - 95533 RMVar_ID_95533 Human_SNP_ID_693170190 m1A Human chr21 - 31659728 31659728 31659728 GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCAACGGAAACCCCAGACGCTGCAGGAGACTACGA GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCGACGGAAACCCCAGACGCTGCAGGAGACTACGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:31659651..31659900 26863196 MeRIP-seq:(Medium) rs755349211 Functional Loss SNV dbSNP153 33..33 33 - - - 95534 RMVar_ID_95534 Human_SNP_ID_693170191 m1A Human chr21 - 31659728 31659728 31659728 GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCAACGGAAACCCCAGACGCTGCAGGAGACTACGA GGCCACGCCGAGGTCCTGGTTCCGAGGACTGCCACGGAAACCCCAGACGCTGCAGGAGACTACGA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:31659651..31659900 26863196 MeRIP-seq:(Medium) rs755349211 Functional Loss SNV dbSNP153 33..33 33 - - - 95535 RMVar_ID_95535 Human_SNP_ID_693170249 m1A Human chr21 + 31659804 31659804 31659804 GGCGACGAAGGCCGTGTGCGTGCTGAAGGGCGACGGCCCAGTGCAGGGCATCATCAATTTCGAGC GGCGACGAAGGCCGTGTGCGTGCTGAAGGGCGCCGGCCCAGTGCAGGGCATCATCAATTTCGAGC A C SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr21:31659676..31659842;chr21:31659676..31659875 26863196,26863410 MeRIP-seq:(Medium) rs1568807374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63775,Human_RBP_ID_245053,Human_RBP_ID_570635,Human_RBP_ID_780146,Human_RBP_ID_928521,Human_RBP_ID_1602604,Human_RBP_ID_1934982,Human_RBP_ID_4679870,Human_RBP_ID_5323483,Human_RBP_ID_7036450,Human_RBP_ID_8540642,Human_RBP_ID_9332086,Human_RBP_ID_9444152,Human_RBP_ID_17659763,Human_RBP_ID_22453862,Human_RBP_ID_27026133,Human_RBP_ID_27489453 Human_miRNA_ID_1967979,Human_miRNA_ID_2381660,Human_miRNA_ID_3024669,Human_miRNA_ID_3091394 RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 95536 RMVar_ID_95536 Human_SNP_ID_693170273 m1A Human chr21 + 31659834 31659834 31659834 CGACGGCCCAGTGCAGGGCATCATCAATTTCGAGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTT CGACGGCCCAGTGCAGGGCATCATCAATTTCGGGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTT A G SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:31659676..31659859 26863196 MeRIP-seq:(Medium) rs1568807435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245053,Human_RBP_ID_928521,Human_RBP_ID_4680203,Human_RBP_ID_5323483,Human_RBP_ID_9332361,Human_RBP_ID_17659679,Human_RBP_ID_22261870 RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 95537 RMVar_ID_95537 Human_SNP_ID_693170275 m1A Human chr21 + 31659837 31659837 31659837 CGGCCCAGTGCAGGGCATCATCAATTTCGAGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTTTGC CGGCCCAGTGCAGGGCATCATCAATTTCGAGCGGAAGGCAAGGGCTGGGACGGAGGCTTGTTTGC A G SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:31659651..31659850 26863196 MeRIP-seq:(Medium) rs1169198442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245053,Human_RBP_ID_4680203,Human_RBP_ID_17659679,Human_RBP_ID_19110567,Human_RBP_ID_22261870 GWAS_ID_12591 RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 95538 RMVar_ID_95538 Human_SNP_ID_693170276 m1A Human chr21 + 31659837 31659837 31659837 CGGCCCAGTGCAGGGCATCATCAATTTCGAGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTTTGC CGGCCCAGTGCAGGGCATCATCAATTTCGAGCTGAAGGCAAGGGCTGGGACGGAGGCTTGTTTGC A T SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:31659651..31659850 26863196 MeRIP-seq:(Medium) rs1169198442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245053,Human_RBP_ID_4680203,Human_RBP_ID_17659679,Human_RBP_ID_19110567,Human_RBP_ID_22261870 GWAS_ID_12591 RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 95539 RMVar_ID_95539 Human_SNP_ID_693172890 m1A Human chr21 + 31668525 31668525 31668525 TGGGCAAAGGTGGAAATGAAGAAAGTACAAAGACAGGAAACGCTGGAAGTCGTTTGGCTTGTGGT TGGGCAAAGGTGGAAATGAAGAAAGTACAAAGGCAGGAAACGCTGGAAGTCGTTTGGCTTGTGGT A G SOD1 Ensembl:ENSG00000142168 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:31668441..31668608 26863196 MeRIP-seq:(Medium) rs1568811445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1602624,Human_RBP_ID_1934992,Human_RBP_ID_3660204,Human_RBP_ID_8540658,Human_RBP_ID_9121725,Human_RBP_ID_14235857,Human_RBP_ID_17513337,Human_RBP_ID_17659534,Human_RBP_ID_22454218,Human_RBP_ID_23212548 Human_Splice_Rec_2114446,Human_Splice_Rec_2114458,Human_Splice_Rec_2114466 RMVar_hsa_circ_211723 95540 RMVar_ID_95540 Human_SNP_ID_693177673 m1A Human chr21 + 31685614 31685611 31685614 ATTGGGTTGAATCCTGGGCGCAAAAATGGTGGAGGAGGAGGGGGAGGAGGAACACCAGGACCAAA ATTGGGTTGAATCCTGGGCGCAAAAATGGT___GGAGGAGGGGGAGGAGGAACACCAGGACCAAA TGGA T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:31685488..31685725 26863196 MeRIP-seq:(Medium) rs3841743 Functional Loss DEL dbSNP153 31..33 33 - - - 95541 RMVar_ID_95541 Human_SNP_ID_693180868 m1A Human chr21 - 31696664 31696664 31696664 AAGAAAGAGGATACCACTGCCGTCACCACGACAGCACCTGCTGCCGCAGTACCCCCTGCACCCAC AAGAAAGAGGATACCACTGCCGTCACCACGACGGCACCTGCTGCCGCAGTACCCCCTGCACCCAC T C SCAF4 Ensembl:ENSG00000156304 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:31696615..31696690 26863196 MeRIP-seq:(Medium) rs749084948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570693,Human_RBP_ID_17397769 Human_Splice_Rec_2114480,Human_Splice_Rec_2114481,Human_Splice_Rec_2114518,Human_Splice_Rec_2114519,Human_Splice_Rec_2114554,Human_Splice_Rec_2114555,Human_Splice_Rec_2114582,Human_Splice_Rec_2114583 Human_miRNA_ID_600830,Human_miRNA_ID_2224277,Human_miRNA_ID_2487350,Human_miRNA_ID_3075717 RMVar_hsa_circ_25070,RMVar_hsa_circ_307880,RMVar_hsa_circ_372592,RMVar_hsa_circ_286862,RMVar_hsa_circ_58772,RMVar_hsa_circ_124608,RMVar_hsa_circ_211725,RMVar_hsa_circ_211726,RMVar_hsa_circ_211724,RMVar_hsa_circ_88044,RMVar_hsa_circ_114471,RMVar_hsa_circ_211732,RMVar_hsa_circ_211733,RMVar_hsa_circ_211731,RMVar_hsa_circ_329754,RMVar_hsa_circ_30450,RMVar_hsa_circ_6664,RMVar_hsa_circ_211735 95542 RMVar_ID_95542 Human_SNP_ID_693190893 m1A Human chr21 - 31732019 31732019 31732019 CCGCCCGCTCGCCGGCCGGGCCAGTGTGAGCCAGTGCGTGAGGGCGCGGGGGGCCGTGTCAGCGA CCGCCCGCTCGCCGGCCGGGCCAGTGTGAGCCGGTGCGTGAGGGCGCGGGGGGCCGTGTCAGCGA T C SCAF4 Ensembl:ENSG00000156304 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:31731971..31732096 26863196 MeRIP-seq:(Medium) rs1400503276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245436,Human_RBP_ID_780669,Human_RBP_ID_4668115,Human_RBP_ID_9391361,Human_RBP_ID_18423348,Human_RBP_ID_26344228,Human_RBP_ID_27820590 95543 RMVar_ID_95543 Human_SNP_ID_693204299 m1A Human chr21 + 31785224 31785213 31785225 TCACCACCATCACCACCACCACCACCACCACCATCACCACCACCATCATCACCATCACCACCACC TCACCACCATCACCACCACCAC____________CACCACCACCATCATCACCATCACCACCACC CCACCACCACCAT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:31785162..31785302 26863196 MeRIP-seq:(Medium) rs1568891585 Functional Loss DEL dbSNP153 23..34 33 - - - 95544 RMVar_ID_95544 Human_SNP_ID_693320032 m1A Human chr21 - 32268853 32268853 32268853 TTGGGAGGTTGAGGCTGCAGTGAGCCTTGGTCATGCCACTACTGTGTTCTAGTCTGGGCAACAGA TTGGGAGGTTGAGGCTGCAGTGAGCCTTGGTCGTGCCACTACTGTGTTCTAGTCTGGGCAACAGA T C MIS18A Ensembl:ENSG00000159055 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:32268751..32269050 32194978 MeRIP-seq:(Medium) rs973499850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570726,Human_RBP_ID_1381187,Human_RBP_ID_4680954,Human_RBP_ID_7037572,Human_RBP_ID_10032742,Human_RBP_ID_14242353,Human_RBP_ID_18779270,Human_RBP_ID_23212553,Human_RBP_ID_23923317 95545 RMVar_ID_95545 Human_SNP_ID_693322686 m1A Human chr21 + 32278964 32278962 32278964 GAGTCGCTGCATTTGCCCTTGTCGCCGCACTCACAGCCGCCAGCGCATCCTCTGCTACACCTCAG GAGTCGCTGCATTTGCCCTTGTCGCCGCACT__CAGCCGCCAGCGCATCCTCTGCTACACCTCAG TCA T MIS18A-AS1 Ensembl:ENSG00000227256 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:32278822..32279069 26863410 MeRIP-seq:(Medium) rs778201325 Functional Loss DEL dbSNP153 32..33 33 - - - 95546 RMVar_ID_95546 Human_SNP_ID_693322715 m1A Human chr21 + 32278995 32278995 32278995 CACAGCCGCCAGCGCATCCTCTGCTACACCTCAGTGACCGAACGCCTGCCATTACCTACAAATCG CACAGCCGCCAGCGCATCCTCTGCTACACCTCCGTGACCGAACGCCTGCCATTACCTACAAATCG A C MIS18A-AS1 Ensembl:ENSG00000227256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32274872..32279050 26863196 MeRIP-seq:(Medium) rs769652796 Functional Loss SNV dbSNP153 33..33 33 - - - 95547 RMVar_ID_95547 Human_SNP_ID_693322716 m1A Human chr21 + 32278995 32278995 32278995 CACAGCCGCCAGCGCATCCTCTGCTACACCTCAGTGACCGAACGCCTGCCATTACCTACAAATCG CACAGCCGCCAGCGCATCCTCTGCTACACCTCGGTGACCGAACGCCTGCCATTACCTACAAATCG A G MIS18A-AS1 Ensembl:ENSG00000227256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32274872..32279050 26863196 MeRIP-seq:(Medium) rs769652796 Functional Loss SNV dbSNP153 33..33 33 - - - 95548 RMVar_ID_95548 Human_SNP_ID_693322717 m1A Human chr21 + 32278995 32278995 32278995 CACAGCCGCCAGCGCATCCTCTGCTACACCTCAGTGACCGAACGCCTGCCATTACCTACAAATCG CACAGCCGCCAGCGCATCCTCTGCTACACCTCTGTGACCGAACGCCTGCCATTACCTACAAATCG A T MIS18A-AS1 Ensembl:ENSG00000227256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32274872..32279050 26863196 MeRIP-seq:(Medium) rs769652796 Functional Loss SNV dbSNP153 33..33 33 - - - 95549 RMVar_ID_95549 Human_SNP_ID_693337765 m1A Human chr21 - 32335077 32335077 32335077 TGGAAGCATTTCCATTCCATCTGGGAGACAGCAGGGAAGCATTCCTCGTCACAGCTGGGCTCTGG TGGAAGCATTTCCATTCCATCTGGGAGACAGCGGGGAAGCATTCCTCGTCACAGCTGGGCTCTGG T C URB1 Ensembl:ENSG00000142207 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32335070..32335296 26863196 MeRIP-seq:(Medium) rs1250993144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14851,RMVar_hsa_circ_42786,RMVar_hsa_circ_78541,RMVar_hsa_circ_5031,RMVar_hsa_circ_269601,RMVar_hsa_circ_211747 95550 RMVar_ID_95550 Human_SNP_ID_693338357 m1A Human chr21 - 32337304 32337304 32337304 TAGGGAATGAGAGCTGGAGGGATGTGAGCAGGAGGAGACAGTGAGACCAGGCGGTGCAAGCAGGG TAGGGAATGAGAGCTGGAGGGATGTGAGCAGGGGGAGACAGTGAGACCAGGCGGTGCAAGCAGGG T C URB1 Ensembl:ENSG00000142207 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32337286..32337377 26863196 MeRIP-seq:(Medium) rs1468887064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26789029 RMVar_hsa_circ_14851,RMVar_hsa_circ_42786,RMVar_hsa_circ_126667,RMVar_hsa_circ_78541,RMVar_hsa_circ_5031,RMVar_hsa_circ_269601,RMVar_hsa_circ_211747,RMVar_hsa_circ_211749,RMVar_hsa_circ_110931,RMVar_hsa_circ_211748 95551 RMVar_ID_95551 Human_SNP_ID_693353088 m1A Human chr21 + 32392918 32392918 32392918 AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGAGGGCGGAAGCGCGACGGAAACGACACACCTGA AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGCGGGCGGAAGCGCGACGGAAACGACACACCTGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32392869..32392978 26863196 MeRIP-seq:(Medium) rs373827834 Functional Loss SNV dbSNP153 33..33 33 - - - 95552 RMVar_ID_95552 Human_SNP_ID_693353089 m1A Human chr21 + 32392918 32392918 32392918 AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGAGGGCGGAAGCGCGACGGAAACGACACACCTGA AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGGGGGCGGAAGCGCGACGGAAACGACACACCTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32392869..32392978 26863196 MeRIP-seq:(Medium) rs373827834 Functional Loss SNV dbSNP153 33..33 33 - - - 95553 RMVar_ID_95553 Human_SNP_ID_693353090 m1A Human chr21 + 32392918 32392918 32392918 AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGAGGGCGGAAGCGCGACGGAAACGACACACCTGA AGGCCTTCCTCTTGGGGACCCCCATGGCCGAGTGGGCGGAAGCGCGACGGAAACGACACACCTGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32392869..32392978 26863196 MeRIP-seq:(Medium) rs373827834 Functional Loss SNV dbSNP153 33..33 33 - - - 95554 RMVar_ID_95554 Human_SNP_ID_693357853 m1A Human chr21 + 32411723 32411723 32411723 CGAACTTGGCAGGCCCTCCCGCCGGGTTCGGGAACACTGTGTGCCTAGCGCCCGCCCTCCTCCCT CGAACTTGGCAGGCCCTCCCGCCGGGTTCGGGGACACTGTGTGCCTAGCGCCCGCCCTCCTCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:32411674..32411881 26863196 MeRIP-seq:(Medium) rs1186696096 Functional Loss SNV dbSNP153 33..33 33 - - - 95555 RMVar_ID_95555 Human_SNP_ID_693358137 m1A Human chr21 - 32412790 32412786 32412790 CCCGGGACGCGCTGGGGGTCGCAGGGCTAAGGACGGCGTCACATGGCGGGGAGAATCGATGGCCA CCCGGGACGCGCTGGGGGTCGCAGGGCTAAGG____CGTCACATGGCGGGGAGAATCGATGGCCA GCCGT G CFAP298-TCP10L Ensembl:ENSG00000265590 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32412739..32412975 26863196 MeRIP-seq:(Medium) rs1033047304 Functional Loss DEL dbSNP153 33..36 33 - - - 95556 RMVar_ID_95556 Human_SNP_ID_693358180 m1A Human chr21 + 32412868 32412868 32412868 CCCGCCGCGCAGCGCACGATGCTTCTGCCGGGACGCGCACGCCAACCGCCGACGCCCCAGCCCGT CCCGCCGCGCAGCGCACGATGCTTCTGCCGGGGCGCGCACGCCAACCGCCGACGCCCCAGCCCGT A G EVA1C Ensembl:ENSG00000166979 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32412697..32412952 26863196 MeRIP-seq:(Medium) rs1156698396 Functional Loss SNV dbSNP153 33..33 33 - - - 95557 RMVar_ID_95557 Human_SNP_ID_693366665 m1A Human chr21 + 32448940 32448936 32448940 GGAGAAAAGAGAGAAAGAAAGAAAGAGAGAGAAAGAGAGAAAGAAAGAAAAGAGAAAGAAAAAGA GGAGAAAAGAGAGAAAGAAAGAAAGAGAG____AGAGAGAAAGAAAGAAAAGAGAAAGAAAAAGA GAGAA G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32448929..32449093 26863196 MeRIP-seq:(Medium) rs1201875266 Functional Loss DEL dbSNP153 30..33 33 - - - 95558 RMVar_ID_95558 Human_SNP_ID_693366670 m1A Human chr21 + 32448940 32448940 32448940 GGAGAAAAGAGAGAAAGAAAGAAAGAGAGAGAAAGAGAGAAAGAAAGAAAAGAGAAAGAAAAAGA GGAGAAAAGAGAGAAAGAAAGAAAGAGAGAGAGAGAGAGAAAGAAAGAAAAGAGAAAGAAAAAGA A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32448929..32449093 26863196 MeRIP-seq:(Medium) rs201627028 Functional Loss SNV dbSNP153 33..33 33 - - - 95559 RMVar_ID_95559 Human_SNP_ID_693366688 m1A Human chr21 + 32448955 32448954 32448955 AGAAAGAAAGAGAGAGAAAGAGAGAAAGAAAGAAAAGAGAAAGAAAAAGAAAGAAAGAAAGAGAG AGAAAGAAAGAGAGAGAAAGAGAGAAAGAAAG_AAAGAGAAAGAAAAAGAAAGAAAGAAAGAGAG GA G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32448953..32449100 26863196 MeRIP-seq:(Medium) rs371906255 Functional Loss DEL dbSNP153 33..33 33 - - - 95560 RMVar_ID_95560 Human_SNP_ID_693369086 m1A Human chr21 - 32459085 32459085 32459085 GTGAGTGTGAGGAGCGTCTGTTATGTGCTGTGAGAGTGTGAGTGCCTTTGCGTGTGCTGTGTTAG GTGAGTGTGAGGAGCGTCTGTTATGTGCTGTGGGAGTGTGAGTGCCTTTGCGTGTGCTGTGTTAG T C CFAP298-TCP10L Ensembl:ENSG00000265590 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:32459073..32459138 26863196 MeRIP-seq:(Medium) rs937567321 Functional Loss SNV dbSNP153 33..33 33 - - - 95561 RMVar_ID_95561 Human_SNP_ID_693376639 m1A Human chr21 - 32491308 32491308 32491308 GTCCGACTCCTCAGAACTGTGCACAAGGCCCCATATGACTTGCCTTTTCTACCTTCCTAGCTCCT GTCCGACTCCTCAGAACTGTGCACAAGGCCCCGTATGACTTGCCTTTTCTACCTTCCTAGCTCCT T C CFAP298-TCP10L Ensembl:ENSG00000265590 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32491164..32491355 26863196 MeRIP-seq:(Medium) rs953598012 Functional Loss SNV dbSNP153 33..33 33 - - - 95562 RMVar_ID_95562 Human_SNP_ID_693403328 m1A Human chr21 - 32603212 32603212 32603212 GCCAAGGAGCTGAGAAGAACGAAGAAGCTTTCAGACTACGTGGGGAAGAATGAAAAAACCAAAAT GCCAAGGAGCTGAGAAGAACGAAGAAGCTTTCGGACTACGTGGGGAAGAATGAAAAAACCAAAAT T C CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr21:32603129..32603273;chr21:32603120..32604237 26863196 MeRIP-seq:(Medium) rs752652841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64688,Human_RBP_ID_570808,Human_RBP_ID_1602910,Human_RBP_ID_1935303,Human_RBP_ID_2701104,Human_RBP_ID_5119551,Human_RBP_ID_7038230,Human_RBP_ID_9391371,Human_RBP_ID_14248033,Human_RBP_ID_18534880,Human_RBP_ID_23923602,Human_RBP_ID_26344240,Human_RBP_ID_27820598 Human_Splice_Rec_2114794,Human_Splice_Rec_2114795,Human_Splice_Rec_2114816,Human_Splice_Rec_2114817,Human_Splice_Rec_2114838,Human_Splice_Rec_2114839,Human_Splice_Rec_2114860,Human_Splice_Rec_2114861,Human_Splice_Rec_2114872,Human_Splice_Rec_2114873,Human_Splice_Rec_2114890,Human_Splice_Rec_2114891,Human_Splice_Rec_2114912,Human_Splice_Rec_2114913,Human_Splice_Rec_2114925,Human_Splice_Rec_2114942,Human_Splice_Rec_2114943,Human_Splice_Rec_2114960,Human_Splice_Rec_2114961,Human_Splice_Rec_2114980,Human_Splice_Rec_2114981,Human_Splice_Rec_2114996,Human_Splice_Rec_2114997,Human_Splice_Rec_2115016,Human_Splice_Rec_2115017,Human_Splice_Rec_2115030,Human_Splice_Rec_2115031,Human_Splice_Rec_2115048,Human_Splice_Rec_2115049,Human_Splice_Rec_2115060,Human_Splice_Rec_2115061,Human_Splice_Rec_2115078,Human_Splice_Rec_2115079,Human_Splice_Rec_2115088,Human_Splice_Rec_2115089,Human_Splice_Rec_2115102,Human_Splice_Rec_2115103,Human_Splice_Rec_2115116,Human_Splice_Rec_2115117,Human_Splice_Rec_2115126,Human_Splice_Rec_2115127,Human_Splice_Rec_2115138,Human_Splice_Rec_2115139,Human_Splice_Rec_2115373,Human_Splice_Rec_2115382,Human_Splice_Rec_2115383,Human_Splice_Rec_2115394,Human_Splice_Rec_2115395,Human_Splice_Rec_2115404,Human_Splice_Rec_2115406,Human_Splice_Rec_2115407,Human_Splice_Rec_2115414,Human_Splice_Rec_2115415,Human_Splice_Rec_2115420,Human_Splice_Rec_2115428 RMVar_hsa_circ_417,RMVar_hsa_circ_70106,RMVar_hsa_circ_356776 95563 RMVar_ID_95563 Human_SNP_ID_693403329 m1A Human chr21 - 32603219 32603217 32603220 GTGGGCAGCCAAGGAGCTGAGAAGAACGAAGAAGCTTTCAGACTACGTGGGGAAGAATGAAAAAA GTGGGCAGCCAAGGAGCTGAGAAGAACGAAG___CTTTCAGACTACGTGGGGAAGAATGAAAAAA GCTT G CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:32603150..32604328 32194978 MeRIP-seq:(Medium) rs1458975548 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1602910,Human_RBP_ID_1935303,Human_RBP_ID_2701105,Human_RBP_ID_4668648,Human_RBP_ID_5119551,Human_RBP_ID_7038230,Human_RBP_ID_9391371,Human_RBP_ID_14248033,Human_RBP_ID_23923603,Human_RBP_ID_26344240,Human_RBP_ID_27820598 Human_Splice_Rec_2114794,Human_Splice_Rec_2114795,Human_Splice_Rec_2114816,Human_Splice_Rec_2114817,Human_Splice_Rec_2114838,Human_Splice_Rec_2114839,Human_Splice_Rec_2114860,Human_Splice_Rec_2114861,Human_Splice_Rec_2114872,Human_Splice_Rec_2114873,Human_Splice_Rec_2114890,Human_Splice_Rec_2114891,Human_Splice_Rec_2114912,Human_Splice_Rec_2114913,Human_Splice_Rec_2114925,Human_Splice_Rec_2114942,Human_Splice_Rec_2114943,Human_Splice_Rec_2114960,Human_Splice_Rec_2114961,Human_Splice_Rec_2114980,Human_Splice_Rec_2114981,Human_Splice_Rec_2114996,Human_Splice_Rec_2114997,Human_Splice_Rec_2115016,Human_Splice_Rec_2115017,Human_Splice_Rec_2115030,Human_Splice_Rec_2115031,Human_Splice_Rec_2115048,Human_Splice_Rec_2115049,Human_Splice_Rec_2115060,Human_Splice_Rec_2115061,Human_Splice_Rec_2115078,Human_Splice_Rec_2115079,Human_Splice_Rec_2115088,Human_Splice_Rec_2115089,Human_Splice_Rec_2115102,Human_Splice_Rec_2115103,Human_Splice_Rec_2115116,Human_Splice_Rec_2115117,Human_Splice_Rec_2115126,Human_Splice_Rec_2115127,Human_Splice_Rec_2115138,Human_Splice_Rec_2115139,Human_Splice_Rec_2115373,Human_Splice_Rec_2115382,Human_Splice_Rec_2115383,Human_Splice_Rec_2115394,Human_Splice_Rec_2115395,Human_Splice_Rec_2115404,Human_Splice_Rec_2115406,Human_Splice_Rec_2115407,Human_Splice_Rec_2115414,Human_Splice_Rec_2115415,Human_Splice_Rec_2115420,Human_Splice_Rec_2115428 RMVar_hsa_circ_417,RMVar_hsa_circ_70106,RMVar_hsa_circ_356776 95564 RMVar_ID_95564 Human_SNP_ID_693403331 m1A Human chr21 - 32603219 32603219 32603219 GTGGGCAGCCAAGGAGCTGAGAAGAACGAAGAAGCTTTCAGACTACGTGGGGAAGAATGAAAAAA GTGGGCAGCCAAGGAGCTGAGAAGAACGAAGACGCTTTCAGACTACGTGGGGAAGAATGAAAAAA T G CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:32603150..32604328 32194978 MeRIP-seq:(Medium) rs1206558583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1602910,Human_RBP_ID_1935303,Human_RBP_ID_2701105,Human_RBP_ID_4668648,Human_RBP_ID_5119551,Human_RBP_ID_7038230,Human_RBP_ID_9391371,Human_RBP_ID_14248033,Human_RBP_ID_23923603,Human_RBP_ID_26344240,Human_RBP_ID_27820598 Human_Splice_Rec_2114794,Human_Splice_Rec_2114795,Human_Splice_Rec_2114816,Human_Splice_Rec_2114817,Human_Splice_Rec_2114838,Human_Splice_Rec_2114839,Human_Splice_Rec_2114860,Human_Splice_Rec_2114861,Human_Splice_Rec_2114872,Human_Splice_Rec_2114873,Human_Splice_Rec_2114890,Human_Splice_Rec_2114891,Human_Splice_Rec_2114912,Human_Splice_Rec_2114913,Human_Splice_Rec_2114925,Human_Splice_Rec_2114942,Human_Splice_Rec_2114943,Human_Splice_Rec_2114960,Human_Splice_Rec_2114961,Human_Splice_Rec_2114980,Human_Splice_Rec_2114981,Human_Splice_Rec_2114996,Human_Splice_Rec_2114997,Human_Splice_Rec_2115016,Human_Splice_Rec_2115017,Human_Splice_Rec_2115030,Human_Splice_Rec_2115031,Human_Splice_Rec_2115048,Human_Splice_Rec_2115049,Human_Splice_Rec_2115060,Human_Splice_Rec_2115061,Human_Splice_Rec_2115078,Human_Splice_Rec_2115079,Human_Splice_Rec_2115088,Human_Splice_Rec_2115089,Human_Splice_Rec_2115102,Human_Splice_Rec_2115103,Human_Splice_Rec_2115116,Human_Splice_Rec_2115117,Human_Splice_Rec_2115126,Human_Splice_Rec_2115127,Human_Splice_Rec_2115138,Human_Splice_Rec_2115139,Human_Splice_Rec_2115373,Human_Splice_Rec_2115382,Human_Splice_Rec_2115383,Human_Splice_Rec_2115394,Human_Splice_Rec_2115395,Human_Splice_Rec_2115404,Human_Splice_Rec_2115406,Human_Splice_Rec_2115407,Human_Splice_Rec_2115414,Human_Splice_Rec_2115415,Human_Splice_Rec_2115420,Human_Splice_Rec_2115428 RMVar_hsa_circ_417,RMVar_hsa_circ_70106,RMVar_hsa_circ_356776 95565 RMVar_ID_95565 Human_SNP_ID_693403538 m1A Human chr21 + 32604084 32604084 32604084 AGGGGCATCAAATCTTAAGGGCTTTGGGGGCCAGGAACTCAACCTCCAGAGTACCCACTCACAAA AGGGGCATCAAATCTTAAGGGCTTTGGGGGCCGGGAACTCAACCTCCAGAGTACCCACTCACAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32604079..32604212 26863196 MeRIP-seq:(Medium) rs1243061686 Functional Loss SNV dbSNP153 33..33 33 - - - 95566 RMVar_ID_95566 Human_SNP_ID_693404998 m1A Human chr21 + 32609858 32609858 32609858 ATCCTCACTTACCTTGCCCATTCCTTCGTCCAATATCATCCTTTTTAAACACTGCACCTCCGCTG ATCCTCACTTACCTTGCCCATTCCTTCGTCCAGTATCATCCTTTTTAAACACTGCACCTCCGCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:32607626..32612584;chr21:32609826..32609875 26863196 MeRIP-seq:(Medium) rs775768955 Functional Loss SNV dbSNP153 33..33 33 - - - 95567 RMVar_ID_95567 Human_SNP_ID_693405758 m1A Human chr21 - 32612215 32612215 32612215 CGCCATGGTTCTGCTGCACGTGAAGCGGGGCGACGAGAGCCAGTTCCTGCTGCAGGCGCCTGGGA CGCCATGGTTCTGCTGCACGTGAAGCGGGGCGGCGAGAGCCAGTTCCTGCTGCAGGCGCCTGGGA T C CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32612171..32612360 26863196 MeRIP-seq:(Medium) rs11538142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245443,Human_RBP_ID_8860659 95568 RMVar_ID_95568 Human_SNP_ID_693405812 m1A Human chr21 - 32612301 32612301 32612301 TGCTGGCGATCCGGCGACCCTCGGCCGGCAGGACCCGCGGGCCACGCAGCCGGGGCCTTCTCAAC TGCTGGCGATCCGGCGACCCTCGGCCGGCAGGGCCCGCGGGCCACGCAGCCGGGGCCTTCTCAAC T C CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:32612176..32612375 26863410 MeRIP-seq:(Medium) rs1166503918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245444,Human_RBP_ID_4668679,Human_RBP_ID_5240578,Human_RBP_ID_5323484,Human_RBP_ID_9299224,Human_RBP_ID_9332366,Human_RBP_ID_22083321 95569 RMVar_ID_95569 Human_SNP_ID_693405818 m1A Human chr21 + 32612333 32612333 32612333 TCCTGCCGGCCGAGGGTCGCCGGATCGCCAGCAGCTGCGACGCACTAACAGCCGCTCACAGTCCG TCCTGCCGGCCGAGGGTCGCCGGATCGCCAGCTGCTGCGACGCACTAACAGCCGCTCACAGTCCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32612286..32612363 26863196 MeRIP-seq:(Medium) rs183552706 Functional Loss SNV dbSNP153 33..33 33 - - - 95570 RMVar_ID_95570 Human_SNP_ID_693432376 m1A Human chr21 + 32726914 32726914 32726914 TTACTGAACGCCATTCTCCTTTCTTCGGAGGCAGCCCTGCGAAAACCAAGCAAAGCAAAGCAAAT TTACTGAACGCCATTCTCCTTTCTTCGGAGGCTGCCCTGCGAAAACCAAGCAAAGCAAAGCAAAT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:32726890..32726974 26863196 MeRIP-seq:(Medium) rs1447119337 Functional Loss SNV dbSNP153 33..33 33 - - - 95571 RMVar_ID_95571 Human_SNP_ID_693562644 m1A Human chr21 + 33264250 33264250 33264250 AAAATAGTAGCAAGAGCTGCAAAGCAGGCAGGAAGGGAGGAGGAGAGCCAGGTGAGCAGTGGAGA AAAATAGTAGCAAGAGCTGCAAAGCAGGCAGGCAGGGAGGAGGAGAGCCAGGTGAGCAGTGGAGA A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33264137..33264341 26863196 MeRIP-seq:(Medium) rs45602836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7039147 Human_miRNA_ID_544831 RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 95572 RMVar_ID_95572 Human_SNP_ID_693563323 m1A Human chr21 - 33266467 33266467 33266467 AGCCACCCAGCCAGCTCCCAAGGCTCCACGCCATGGACGGACGCTGGGGGTTCCGCGGCTTCCTC AGCCACCCAGCCAGCTCCCAAGGCTCCACGCCGTGGACGGACGCTGGGGGTTCCGCGGCTTCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33266417..33266592 26863196 MeRIP-seq:(Medium) rs753430996 Functional Loss SNV dbSNP153 33..33 33 - - - 95573 RMVar_ID_95573 Human_SNP_ID_693566023 m1A Human chr21 + 33277094 33277094 33277094 CTGGGAGAAAGTCAGTATGGAATTATGACTTAAACAAAGAAACATAACGTGATAGGCAAAAGAAT CTGGGAGAAAGTCAGTATGGAATTATGACTTAGACAAAGAAACATAACGTGATAGGCAAAAGAAT A G IL10RB,AP000295.1 Ensembl:ENSG00000243646,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33277078..33277162 26863196 MeRIP-seq:(Medium) rs774258179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2701378 RMVar_hsa_circ_211825,RMVar_hsa_circ_101521,RMVar_hsa_circ_15152,RMVar_hsa_circ_311244,RMVar_hsa_circ_362069,RMVar_hsa_circ_211836,RMVar_hsa_circ_333411,RMVar_hsa_circ_211837,RMVar_hsa_circ_211838 95574 RMVar_ID_95574 Human_SNP_ID_693570903 m1A Human chr21 + 33296869 33296869 33296869 ACTCGAGTGCCTGAGGCAGGAGAATTGCATGAACCCGGGAGGAGGAGGAGGAGGTTGCAGTGAGC ACTCGAGTGCCTGAGGCAGGAGAATTGCATGAGCCCGGGAGGAGGAGGAGGAGGTTGCAGTGAGC A G IL10RB,AP000295.1 Ensembl:ENSG00000243646,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33296821..33296966 26863196 MeRIP-seq:(Medium) rs1323537387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570912,Human_RBP_ID_14253610 RMVar_hsa_circ_101521,RMVar_hsa_circ_121156,RMVar_hsa_circ_211838,RMVar_hsa_circ_89036,RMVar_hsa_circ_99432,RMVar_hsa_circ_211839,RMVar_hsa_circ_211842,RMVar_hsa_circ_211843 95575 RMVar_ID_95575 Human_SNP_ID_693579808 m1A Human chr21 - 33325027 33325027 33325027 TCATCTGGGAGCCGCCGCAGATCCCACCAGTTACATGTTCGCGCACGCGCAGCTCCTCTCAGCCG TCATCTGGGAGCCGCCGCAGATCCCACCAGTTGCATGTTCGCGCACGCGCAGCTCCTCTCAGCCG T C lnc-TMEM50B-4,lnc-TMEM50B-4:2 RNACentral:URS00008BFF19,RNACentral:URS0000D57DCC lincRNA,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33324625..33325096 26863196 MeRIP-seq:(Medium) rs751767584 Functional Loss SNV dbSNP153 33..33 33 - - - 95576 RMVar_ID_95576 Human_SNP_ID_693582265 m1A Human chr21 - 33335477 33335477 33335477 AGAAATAAGAACATTATATACAAACTGTACAGATATTCTAAATGTTATTCTATCCCTCACATCCC AGAAATAAGAACATTATATACAAACTGTACAGGTATTCTAAATGTTATTCTATCCCTCACATCCC T C lnc-TMEM50B-4 RNACentral:URS00008BFF19 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33335475..33335547 26863196 MeRIP-seq:(Medium) rs1482491297 Functional Loss SNV dbSNP153 33..33 33 - - - 95577 RMVar_ID_95577 Human_SNP_ID_693587450 m1A Human chr21 + 33355829 33355829 33355829 CATGAGGTCAAGAGATCGAGACCAGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATAC CATGAGGTCAAGAGATCGAGACCAGCCTGGCCGACGTGGTGAAACCCCATCTCTACTAAAAATAC A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs924660967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151209 95578 RMVar_ID_95578 Human_SNP_ID_693602201 m1A Human chr21 - 33414829 33414829 33414829 GGGAGGAAGGGAGGAGAGAGAGGGAAATAATTACAAAAATGTTTCAATGTCCATTATCTAAGTCA GGGAGGAAGGGAGGAGAGAGAGGGAAATAATTTCAAAAATGTTTCAATGTCCATTATCTAAGTCA T A lnc-TMEM50B-3 RNACentral:URS00008BE4E0 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33414827..33414912 26863196 MeRIP-seq:(Medium) rs1267172008 Functional Loss SNV dbSNP153 33..33 33 - - - 95579 RMVar_ID_95579 Human_SNP_ID_693627717 m1A Human chr21 - 33511311 33511311 33511311 ATCAAAGGAGCAGACAGAGCAGATTCTGAGGGATATCCAGCAGCACAAGGAAGAAGCCTGGGTGA ATCAAAGGAGCAGACAGAGCAGATTCTGAGGGGTATCCAGCAGCACAAGGAAGAAGCCTGGGTGA T C GART Ensembl:ENSG00000159131 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8971 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_7039758,Human_RBP_ID_14257032,Human_RBP_ID_17981411,Human_RBP_ID_19006661 Human_Splice_Rec_2116869,Human_Splice_Rec_2116911,Human_Splice_Rec_2116953,Human_Splice_Rec_2116993,Human_Splice_Rec_2117005 GWAS_ID_12592,GWAS_ID_12593,GWAS_ID_12594,GWAS_ID_12595,GWAS_ID_12596 RMVar_hsa_circ_6781,RMVar_hsa_circ_38850,RMVar_hsa_circ_20820,RMVar_hsa_circ_41605,RMVar_hsa_circ_334817,RMVar_hsa_circ_347799,RMVar_hsa_circ_24371 95580 RMVar_ID_95580 Human_SNP_ID_693627747 m1A Human chr21 + 33511419 33511419 33511419 TCTCTTCCTCAGAGAGGTGTCCTTCCTGCTGCAACCATGAGAAGACCCTGGGGATCCTCCAGGTC TCTCTTCCTCAGAGAGGTGTCCTTCCTGCTGCGACCATGAGAAGACCCTGGGGATCCTCCAGGTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:33511368..33520415 32194978 MeRIP-seq:(Medium) rs755176399 Functional Loss SNV dbSNP153 33..33 33 - - - 95581 RMVar_ID_95581 Human_SNP_ID_693631313 m1A Human chr21 + 33524915 33524915 33524915 TTTTCCCGGATGGCTGTGACTGCAAGAACTCTACCCCCATGAGTTACTACTTTGCCATTTTTGAG TTTTCCCGGATGGCTGTGACTGCAAGAACTCTGCCCCCATGAGTTACTACTTTGCCATTTTTGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:33524864..33528329 32194978 MeRIP-seq:(Medium) rs1466075348 Functional Loss SNV dbSNP153 33..33 33 - - - 95582 RMVar_ID_95582 Human_SNP_ID_693631721 m1A Human chr21 - 33526211 33526211 33526211 AGCCGAGGTCGCACAACTGCACACTCCAGCCTAGGTGACAGAGCAAGACTCTGTCCCAAAAAGAA AGCCGAGGTCGCACAACTGCACACTCCAGCCTCGGTGACAGAGCAAGACTCTGTCCCAAAAAGAA T G GART Ensembl:ENSG00000159131 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1329056750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25638748 RMVar_hsa_circ_41605,RMVar_hsa_circ_351341,RMVar_hsa_circ_54071,RMVar_hsa_circ_366176,RMVar_hsa_circ_46203 95583 RMVar_ID_95583 Human_SNP_ID_693636686 m1A Human chr21 + 33543102 33543102 33543102 GTTGAGAGAACGGAGCGGACGCCATGGCGACCAACATCGAGCAGATTTTTAGGTCTTTCGTGGTC GTTGAGAGAACGGAGCGGACGCCATGGCGACCGACATCGAGCAGATTTTTAGGTCTTTCGTGGTC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:33543051..33543215;chr21:33543051..33543218;chr21:33543051..33543227 26863196 MeRIP-seq:(Medium) rs1394326730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245128,Human_RBP_ID_571213,Human_RBP_ID_1027635,Human_RBP_ID_1136258,Human_RBP_ID_1603191,Human_RBP_ID_4679893,Human_RBP_ID_7040010,Human_RBP_ID_8861028,Human_RBP_ID_9299234,Human_RBP_ID_14258386,Human_RBP_ID_23009628,Human_RBP_ID_26344637 Human_Splice_Rec_2117109,Human_Splice_Rec_2117131,Human_Splice_Rec_2117133,Human_Splice_Rec_2117153,Human_Splice_Rec_2117165,Human_Splice_Rec_2117189,Human_Splice_Rec_2117197 RMVar_hsa_circ_121649,RMVar_hsa_circ_211887 95584 RMVar_ID_95584 Human_SNP_ID_693637598 m1A Human chr21 - 33546172 33546170 33546173 GAAAAGTTATCGAAATTCATTAATATTTTATCATACCATTAATAAAAAAATCCAATTAATTACAA GAAAAGTTATCGAAATTCATTAATATTTTAT___ACCATTAATAAAAAAATCCAATTAATTACAA TATG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33546166..33546317 26863196 MeRIP-seq:(Medium) rs761693573 Functional Loss DEL dbSNP153 32..34 33 - - - 95585 RMVar_ID_95585 Human_SNP_ID_693637627 m1A Human chr21 + 33546269 33546269 33546269 TGGTGAAACAAATACACCCATTGAAGGAAACCAGGCGGGTGATGCAGCTGCCTCTGCCAGGAGTC TGGTGAAACAAATACACCCATTGAAGGAAACCCGGCGGGTGATGCAGCTGCCTCTGCCAGGAGTC A C SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33546176..33546293 26863196 MeRIP-seq:(Medium) rs775890214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64020,Human_RBP_ID_4669535,Human_RBP_ID_8858680,Human_RBP_ID_9299235,Human_RBP_ID_14258625,Human_RBP_ID_17978893,Human_RBP_ID_22083333,Human_RBP_ID_24546933,Human_RBP_ID_26344141,Human_RBP_ID_27026641,Human_RBP_ID_27820642 Human_Splice_Rec_2117110,Human_Splice_Rec_2117132,Human_Splice_Rec_2117134,Human_Splice_Rec_2117154,Human_Splice_Rec_2117166,Human_Splice_Rec_2117190,Human_Splice_Rec_2117198 Human_miRNA_ID_1017173,Human_miRNA_ID_1303521 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_359911,RMVar_hsa_circ_211888,RMVar_hsa_circ_211889 95586 RMVar_ID_95586 Human_SNP_ID_693638801 m1A Human chr21 + 33549867 33549867 33549867 TTAGAAACTCTGAAGCCAGCTACAAAAACTGCAGAACTGTCAGTTGTATCTACATCAGTAATCTC TTAGAAACTCTGAAGCCAGCTACAAAAACTGCCGAACTGTCAGTTGTATCTACATCAGTAATCTC A C SON Ensembl:ENSG00000159140 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79746820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1027646,Human_RBP_ID_1603212,Human_RBP_ID_1935747,Human_RBP_ID_2701555,Human_RBP_ID_7040086,Human_RBP_ID_8541238,Human_RBP_ID_8858692,Human_RBP_ID_26344144,Human_RBP_ID_26821722,Human_RBP_ID_27026651,Human_RBP_ID_27301162,Human_RBP_ID_27489655 GWAS_ID_12597,GWAS_ID_12598,GWAS_ID_12599 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95587 RMVar_ID_95587 Human_SNP_ID_693638802 m1A Human chr21 + 33549867 33549867 33549867 TTAGAAACTCTGAAGCCAGCTACAAAAACTGCAGAACTGTCAGTTGTATCTACATCAGTAATCTC TTAGAAACTCTGAAGCCAGCTACAAAAACTGCGGAACTGTCAGTTGTATCTACATCAGTAATCTC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79746820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1027646,Human_RBP_ID_1603212,Human_RBP_ID_1935747,Human_RBP_ID_2701555,Human_RBP_ID_7040086,Human_RBP_ID_8541238,Human_RBP_ID_8858692,Human_RBP_ID_26344144,Human_RBP_ID_26821722,Human_RBP_ID_27026651,Human_RBP_ID_27301162,Human_RBP_ID_27489655 GWAS_ID_12597,GWAS_ID_12598,GWAS_ID_12599 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95588 RMVar_ID_95588 Human_SNP_ID_693638882 m1A Human chr21 + 33550075 33550075 33550075 AGATGAAGTCTGTGCTGAAATCTGTGGAGAGCACATCTCCAGAGCCATCAAAGATCATGTTGGTA AGATGAAGTCTGTGCTGAAATCTGTGGAGAGCGCATCTCCAGAGCCATCAAAGATCATGTTGGTA A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:33550051..33550075 26863196 MeRIP-seq:(Medium) rs759434162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780240,Human_RBP_ID_1603221,Human_RBP_ID_1935756,Human_RBP_ID_3661045,Human_RBP_ID_7040088,Human_RBP_ID_8858699,Human_RBP_ID_9260488,Human_RBP_ID_14258887,Human_RBP_ID_17284026,Human_RBP_ID_17513461,Human_RBP_ID_18779837,Human_RBP_ID_23007231,Human_RBP_ID_26344286,Human_RBP_ID_26494704,Human_RBP_ID_27705217 Human_miRNA_ID_1985563,Human_miRNA_ID_2793936,Human_miRNA_ID_2941212,Human_miRNA_ID_3070329 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95589 RMVar_ID_95589 Human_SNP_ID_693638896 m1A Human chr21 - 33550106 33550106 33550106 AAGGCTCTAACACTTTTGCTACTGGGGGCTCTACCAACATGATCTTTGATGGCTCTGGAGATGTG AAGGCTCTAACACTTTTGCTACTGGGGGCTCTGCCAACATGATCTTTGATGGCTCTGGAGATGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33550057..33550276 26863196 MeRIP-seq:(Medium) rs1208289441 Functional Loss SNV dbSNP153 33..33 33 - - - 95590 RMVar_ID_95590 Human_SNP_ID_693638913 m1A Human chr21 - 33550151 33550149 33550152 GGTACACCTCAGTAGGTGTCTCTGATGATACCACAAGGGTTTCTGAAGGCTCTAACACTTTTGCT GGTACACCTCAGTAGGTGTCTCTGATGATAC___AAGGGTTTCTGAAGGCTCTAACACTTTTGCT TGTG T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:33550101..33550150 26863196 MeRIP-seq:(Medium) rs747540807 Functional Loss DEL dbSNP153 32..34 33 - - - 95591 RMVar_ID_95591 Human_SNP_ID_693639577 m1A Human chr21 + 33551626 33551626 33551626 CTAGCACTATGGACTCCCAGATGTTAGCAACCAGTTCCATGGACTCCCAGATGTTAGCAACCAGC CTAGCACTATGGACTCCCAGATGTTAGCAACCGGTTCCATGGACTCCCAGATGTTAGCAACCAGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33551481..33551675 26863196 MeRIP-seq:(Medium) rs550069949 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1935783,Human_RBP_ID_7040129,Human_RBP_ID_8541279,Human_RBP_ID_8858747,Human_RBP_ID_9122007,Human_RBP_ID_9298869,Human_RBP_ID_10033938,Human_RBP_ID_14258991,Human_RBP_ID_17284033,Human_RBP_ID_17397361,Human_RBP_ID_18779901,Human_RBP_ID_22082157,Human_RBP_ID_23007254,Human_RBP_ID_27026684,Human_RBP_ID_27301182 Human_miRNA_ID_2921426 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95592 RMVar_ID_95592 Human_SNP_ID_693639628 m1A Human chr21 + 33551752 33551748 33551752 CCATGGACTCCCAGATGTTAGCAACCAGCACCATGGATTCTCAGATGTTAGCAACCAGCACCATG CCATGGACTCCCAGATGTTAGCAACCAGC____TGGATTCTCAGATGTTAGCAACCAGCACCATG CACCA C SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33551701..33551775 26863196 MeRIP-seq:(Medium) rs1271628258 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_780250,Human_RBP_ID_1603277,Human_RBP_ID_1935785,Human_RBP_ID_3661061,Human_RBP_ID_7040130,Human_RBP_ID_8858750,Human_RBP_ID_9122008,Human_RBP_ID_14258998,Human_RBP_ID_17284034,Human_RBP_ID_17397362,Human_RBP_ID_22818412,Human_RBP_ID_27026685,Human_RBP_ID_27489690 Human_miRNA_ID_2404650,Human_miRNA_ID_2919701 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95593 RMVar_ID_95593 Human_SNP_ID_693640189 m1A Human chr21 + 33553093 33553093 33553093 CAGAGAGACCAGTGACTTGTATGGTATCTGAAACTCCCGCCATGTCAGCTGAACCAACTGTGTTA CAGAGAGACCAGTGACTTGTATGGTATCTGAACCTCCCGCCATGTCAGCTGAACCAACTGTGTTA A C SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33553043..33553141 26863196 MeRIP-seq:(Medium) rs1489329323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245137,Human_RBP_ID_1027696,Human_RBP_ID_1603319,Human_RBP_ID_1935805,Human_RBP_ID_3661075,Human_RBP_ID_5529547,Human_RBP_ID_7040157,Human_RBP_ID_8114925,Human_RBP_ID_8858798,Human_RBP_ID_9260405,Human_RBP_ID_9298895,Human_RBP_ID_14259085,Human_RBP_ID_18325653,Human_RBP_ID_18779949,Human_RBP_ID_26344292,Human_RBP_ID_26821972,Human_RBP_ID_27026710,Human_RBP_ID_27301201,Human_RBP_ID_27489721,Human_RBP_ID_27705249 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95594 RMVar_ID_95594 Human_SNP_ID_693640335 m1A Human chr21 - 33553397 33553374 33553398 GCTCAGCCACAACAGGAGGCTCCGGGACAGTCACAACCGAAGGCTCCAGGACAGTTACAGTCGAA GCTCAGCCACAACAGGAGGCTCCGGGACAGT________________________TACAGTCGAA AACTGTCCTGGAGCCTTCGGTTGTG A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:33553302..33553411 32194978 MeRIP-seq:(Medium) rs769691894 Functional Loss DEL dbSNP153 32..55 33 - - - Clinvar_Rec_548 95595 RMVar_ID_95595 Human_SNP_ID_693640372 m1A Human chr21 + 33553427 33553427 33553427 TGTGACTGTCCCGGAGCCTCCTGTTGTGGCTGAGCCAGACTATGTTACCATTCCTGTGCCAGTTG TGTGACTGTCCCGGAGCCTCCTGTTGTGGCTGGGCCAGACTATGTTACCATTCCTGTGCCAGTTG A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:33553376..33553534 32194978 MeRIP-seq:(Medium) rs1481905726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1027700,Human_RBP_ID_1100451,Human_RBP_ID_1199670,Human_RBP_ID_1603332,Human_RBP_ID_1935807,Human_RBP_ID_8541311,Human_RBP_ID_8858804,Human_RBP_ID_9299261,Human_RBP_ID_14259128,Human_RBP_ID_18779962,Human_RBP_ID_22768051,Human_RBP_ID_26344293,Human_RBP_ID_27026715 Human_miRNA_ID_337202,Human_miRNA_ID_794779,Human_miRNA_ID_2084563,Human_miRNA_ID_2270691 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95596 RMVar_ID_95596 Human_SNP_ID_693641055 m1A Human chr21 + 33555082 33555082 33555082 CTAGATCTGTGGGTAGAAGAAGGAGCTTTAGCATTTCCCCAAGCCGCCGCAGCCGCACCCCCAGC CTAGATCTGTGGGTAGAAGAAGGAGCTTTAGCGTTTCCCCAAGCCGCCGCAGCCGCACCCCCAGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:33555051..33555225 26863196 MeRIP-seq:(Medium) rs1364217750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1027726,Human_RBP_ID_1603391,Human_RBP_ID_1935832,Human_RBP_ID_4669823,Human_RBP_ID_8541339,Human_RBP_ID_8858866,Human_RBP_ID_14259270,Human_RBP_ID_17978952,Human_RBP_ID_18780021,Human_RBP_ID_22082189,Human_RBP_ID_22262366,Human_RBP_ID_23924360 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95597 RMVar_ID_95597 Human_SNP_ID_693641056 m1A Human chr21 + 33555127 33555085 33555127 GCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGC _________________________________CCCCCAGCCGCCGCAGCCGCACCCCCAGCCGC TCCCCAAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCA T SON Ensembl:ENSG00000159140 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:33555026..33555225 26863410 MeRIP-seq:(Medium) rs773869033 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95598 RMVar_ID_95598 Human_SNP_ID_693641059 m1A Human chr21 + 33555090 33555090 33555090 GTGGGTAGAAGAAGGAGCTTTAGCATTTCCCCAAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAG GTGGGTAGAAGAAGGAGCTTTAGCATTTCCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAG A C SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:33554782..33555291;chr21:33554976..33555284;chr21:33554951..33555300 26863196 MeRIP-seq:(Medium) rs202027184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1027726,Human_RBP_ID_1603391,Human_RBP_ID_1935832,Human_RBP_ID_8541339,Human_RBP_ID_8858866,Human_RBP_ID_17978952,Human_RBP_ID_18780021,Human_RBP_ID_22262366 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95599 RMVar_ID_95599 Human_SNP_ID_693641085 m1A Human chr21 + 33555127 33555127 33555127 GCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGC GCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCGCCCCCAGCCGCCGCAGCCGCACCCCCAGCCGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:33555026..33555225 26863410 MeRIP-seq:(Medium) rs995280288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95600 RMVar_ID_95600 Human_SNP_ID_693641116 m1A Human chr21 + 33555163 33555163 33555163 CCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGGAGCCGCACCCCT CCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCGGCCGCACCCCCAGCCGCCGGAGCCGCACCCCT A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:33555151..33555175 26863196 MeRIP-seq:(Medium) rs967557189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533700 Human_miRNA_ID_2686527 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95601 RMVar_ID_95601 Human_SNP_ID_693641120 m1A Human chr21 + 33555169 33555169 33555169 GCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGGAGCCGCACCCCTAGCCGT GCCGCAGCCGCACCCCCAGCCGCCGCAGCCGCCCCCCCAGCCGCCGGAGCCGCACCCCTAGCCGT A C SON Ensembl:ENSG00000159140 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:33555001..33555275 26863410 MeRIP-seq:(Medium) rs966237964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8860873,Human_RBP_ID_22533700 Human_miRNA_ID_2686527 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 95602 RMVar_ID_95602 Human_SNP_ID_693650428 m1A Human chr21 - 33588569 33588568 33588569 AGCCGCCCGAGGTAGTGCGGCTCCGACGGAAAAGGGCCCGGAGCCGTGGAGCTGCCGCCTCCCCG AGCCGCCCGAGGTAGTGCGGCTCCGACGGAAA_GGGCCCGGAGCCGTGGAGCTGCCGCCTCCCCG CT C AP000311.1,DONSON Ensembl:ENSG00000249209,Ensembl:ENSG00000159147 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:33588524..33588638 26863196 MeRIP-seq:(Medium) rs1443953501 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_245146,Human_RBP_ID_832967,Human_RBP_ID_4679895,Human_RBP_ID_9332101,Human_RBP_ID_18423353,Human_RBP_ID_27840901 RMVar_hsa_circ_107330,RMVar_hsa_circ_211902,RMVar_hsa_circ_77035,RMVar_hsa_circ_211904 95603 RMVar_ID_95603 Human_SNP_ID_693661196 m1A Human chr21 - 33631551 33631551 33631551 TTTCATTTATATATATTTATTTTTAGGTGACTATGAAAGGCTTATATTTCCAACAGAGTTCCACA TTTCATTTATATATATTTATTTTTAGGTGACTGTGAAAGGCTTATATTTCCAACAGAGTTCCACA T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding start codon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33624730..33633693 26863196 MeRIP-seq:(Medium) rs747446935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928085,Human_RBP_ID_3961223,Human_RBP_ID_14262238,Human_RBP_ID_18413029,Human_RBP_ID_25639947 Human_Splice_Rec_2117492,Human_Splice_Rec_2117493,Human_Splice_Rec_2117514,Human_Splice_Rec_2117515,Human_Splice_Rec_2117536,Human_Splice_Rec_2117537,Human_Splice_Rec_2117580,Human_Splice_Rec_2117581,Human_Splice_Rec_2117602,Human_Splice_Rec_2117603,Human_Splice_Rec_2117622,Human_Splice_Rec_2117623,Human_Splice_Rec_2117640,Human_Splice_Rec_2117641,Human_Splice_Rec_2117698,Human_Splice_Rec_2117699,Human_Splice_Rec_2117719,Human_Splice_Rec_2117732,Human_Splice_Rec_2117733,Human_Splice_Rec_2117744,Human_Splice_Rec_2117745,Human_Splice_Rec_2117754 RMVar_hsa_circ_362264,RMVar_hsa_circ_37663,RMVar_hsa_circ_302225,RMVar_hsa_circ_48777,RMVar_hsa_circ_211916,RMVar_hsa_circ_345885,RMVar_hsa_circ_211917,RMVar_hsa_circ_314209 95604 RMVar_ID_95604 Human_SNP_ID_693664358 m1A Human chr21 + 33643032 33643032 33643032 GGGGATGAATGGGCGCCGCGGCCCCGCCGCCGAGCGGGCTCCCTCCTCTCGCGGGGACCCCGGGC GGGGATGAATGGGCGCCGCGGCCCCGCCGCCGGGCGGGCTCCCTCCTCTCGCGGGGACCCCGGGC A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:33643017..33643406 26863196 MeRIP-seq:(Medium) rs995679194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245540,Human_RBP_ID_9431853,Human_RBP_ID_18463768,Human_RBP_ID_26789037 95605 RMVar_ID_95605 Human_SNP_ID_693682546 m1A Human chr21 - 33714318 33714318 33714318 TCCTTCATCTGTATCTCTTAAGTGACAACCAAAGGGACTCCACGTTCTCTCTCTTTCCCTCCCCA TCCTTCATCTGTATCTCTTAAGTGACAACCAAGGGGACTCCACGTTCTCTCTCTTTCCCTCCCCA T C AP000311.1 Ensembl:ENSG00000249209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33714315..33714448 26863196 MeRIP-seq:(Medium) rs1202297700 Functional Loss SNV dbSNP153 33..33 33 - - - 95606 RMVar_ID_95606 Human_SNP_ID_693683001 m1A Human chr21 + 33716394 33716394 33716394 GTGAGCCTGTACAGGTCTGCACACTGAAGTGTAGGGCCCTACCTCCTTCCTTCTTCACTCCTCCT GTGAGCCTGTACAGGTCTGCACACTGAAGTGTGGGGCCCTACCTCCTTCCTTCTTCACTCCTCCT A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33716392..33716464 26863196 MeRIP-seq:(Medium) rs1235632921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311861,RMVar_hsa_circ_338052 95607 RMVar_ID_95607 Human_SNP_ID_693685798 m1A Human chr21 + 33727293 33727292 33727294 GAGGGGAGGAGAATAAAGCAGTGGGAATAGACAAGAGCCAGAAGGTACAGGAAGGAAGAAGAGAC GAGGGGAGGAGAATAAAGCAGTGGGAATAGAC__GAGCCAGAAGGTACAGGAAGGAAGAAGAGAC CAA C ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33727289..33727405 26863196 MeRIP-seq:(Medium) rs1285884504 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_53649,RMVar_hsa_circ_338052,RMVar_hsa_circ_338624,RMVar_hsa_circ_367983,RMVar_hsa_circ_373378,RMVar_hsa_circ_367680,RMVar_hsa_circ_285772,RMVar_hsa_circ_211921,RMVar_hsa_circ_42984,RMVar_hsa_circ_211922,RMVar_hsa_circ_42436,RMVar_hsa_circ_324872,RMVar_hsa_circ_71588,RMVar_hsa_circ_366225 95608 RMVar_ID_95608 Human_SNP_ID_693702176 m1A Human chr21 + 33794466 33794466 33794466 ATAGAATTAGAAAAACAAAAAGAAGAAGCCCAAAGGTGAGTCTTCTTTGGATTGTGGACTCATCT ATAGAATTAGAAAAACAAAAAGAAGAAGCCCACAGGTGAGTCTTCTTTGGATTGTGGACTCATCT A C ITSN1 Ensembl:ENSG00000205726 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:33794351..33794534 26863196 MeRIP-seq:(Medium) rs1160518695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2117791,Human_Splice_Rec_2117865,Human_Splice_Rec_2117923,Human_Splice_Rec_2117997,Human_Splice_Rec_2118073,Human_Splice_Rec_2118129,Human_Splice_Rec_2118183,Human_Splice_Rec_2118235,Human_Splice_Rec_2118339,Human_Splice_Rec_2118373 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_278358,RMVar_hsa_circ_54764,RMVar_hsa_circ_8711,RMVar_hsa_circ_16621,RMVar_hsa_circ_49537,RMVar_hsa_circ_73893,RMVar_hsa_circ_366775,RMVar_hsa_circ_211930,RMVar_hsa_circ_29554,RMVar_hsa_circ_267203,RMVar_hsa_circ_48563,RMVar_hsa_circ_309107,RMVar_hsa_circ_211934,RMVar_hsa_circ_317424,RMVar_hsa_circ_300094,RMVar_hsa_circ_364521,RMVar_hsa_circ_211936 95609 RMVar_ID_95609 Human_SNP_ID_693702919 m1A Human chr21 + 33797510 33797510 33797510 GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGGAAAAAGGCAAACAGGAAGCACAAGACAAGCTGG GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGGGAAAAGGCAAACAGGAAGCACAAGACAAGCTGG A G ITSN1 Ensembl:ENSG00000205726 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33797339..33797550 26863196 MeRIP-seq:(Medium) rs972530973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928089,Human_RBP_ID_5529561,Human_RBP_ID_9391449 Human_Splice_Rec_2117793,Human_Splice_Rec_2117867,Human_Splice_Rec_2117925,Human_Splice_Rec_2117999,Human_Splice_Rec_2118075,Human_Splice_Rec_2118131,Human_Splice_Rec_2118185,Human_Splice_Rec_2118237,Human_Splice_Rec_2118341,Human_Splice_Rec_2118375,Human_Splice_Rec_2118403 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_278358,RMVar_hsa_circ_8711,RMVar_hsa_circ_16621,RMVar_hsa_circ_49537,RMVar_hsa_circ_73893,RMVar_hsa_circ_366775,RMVar_hsa_circ_211930,RMVar_hsa_circ_267203,RMVar_hsa_circ_48563,RMVar_hsa_circ_211934,RMVar_hsa_circ_300094,RMVar_hsa_circ_364521,RMVar_hsa_circ_20438,RMVar_hsa_circ_211936 95610 RMVar_ID_95610 Human_SNP_ID_693707254 m1A Human chr21 + 33815662 33815662 33815662 AGCCATGTTGCCAGTGGAGATGGGAATGGAAAAGTGAAGTGTCAGAGGATATAGTTGGTATAAGG AGCCATGTTGCCAGTGGAGATGGGAATGGAAAGGTGAAGTGTCAGAGGATATAGTTGGTATAAGG A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33815427..33815993 26863196 MeRIP-seq:(Medium) rs1004539361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_8711,RMVar_hsa_circ_267203,RMVar_hsa_circ_364521,RMVar_hsa_circ_60491,RMVar_hsa_circ_349237,RMVar_hsa_circ_56766,RMVar_hsa_circ_23162,RMVar_hsa_circ_39623,RMVar_hsa_circ_317342,RMVar_hsa_circ_324920,RMVar_hsa_circ_324958,RMVar_hsa_circ_48463,RMVar_hsa_circ_211938,RMVar_hsa_circ_211939,RMVar_hsa_circ_373936,RMVar_hsa_circ_211937,RMVar_hsa_circ_329373,RMVar_hsa_circ_211941,RMVar_hsa_circ_211942 95611 RMVar_ID_95611 Human_SNP_ID_693707256 m1A Human chr21 + 33815673 33815673 33815673 CAGTGGAGATGGGAATGGAAAAGTGAAGTGTCAGAGGATATAGTTGGTATAAGGCAGAAAACATT CAGTGGAGATGGGAATGGAAAAGTGAAGTGTCGGAGGATATAGTTGGTATAAGGCAGAAAACATT A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33815459..33815906 26863196 MeRIP-seq:(Medium) rs898896578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14265510 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_8711,RMVar_hsa_circ_267203,RMVar_hsa_circ_364521,RMVar_hsa_circ_60491,RMVar_hsa_circ_349237,RMVar_hsa_circ_56766,RMVar_hsa_circ_23162,RMVar_hsa_circ_39623,RMVar_hsa_circ_317342,RMVar_hsa_circ_324920,RMVar_hsa_circ_324958,RMVar_hsa_circ_48463,RMVar_hsa_circ_211938,RMVar_hsa_circ_211939,RMVar_hsa_circ_373936,RMVar_hsa_circ_211937,RMVar_hsa_circ_329373,RMVar_hsa_circ_211941,RMVar_hsa_circ_211942 95612 RMVar_ID_95612 Human_SNP_ID_693732001 m1A Human chr21 - 33914488 33914488 33914488 TTTCCTTTATTGCTTTGAAGGTGCGATGCTTCAGTACCTCTGTGGTCAGACCATTTGCCAAGCTT TTTCCTTTATTGCTTTGAAGGTGCGATGCTTCGGTACCTCTGTGGTCAGACCATTTGCCAAGCTT T C AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:33585993..33915781 32194978 MeRIP-seq:(Medium) rs1350556542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245542,Human_RBP_ID_571478,Human_RBP_ID_780612,Human_RBP_ID_1027786,Human_RBP_ID_1305767,Human_RBP_ID_1603726,Human_RBP_ID_4679721,Human_RBP_ID_5323489,Human_RBP_ID_9122171,Human_RBP_ID_9332104,Human_RBP_ID_14267031,Human_RBP_ID_18423546,Human_RBP_ID_19110663,Human_RBP_ID_22453896,Human_RBP_ID_22673020,Human_RBP_ID_22818515 Human_Splice_Rec_2117480,Human_Splice_Rec_2117481,Human_Splice_Rec_2118514,Human_Splice_Rec_2118515,Human_Splice_Rec_2118523,Human_Splice_Rec_2118534,Human_Splice_Rec_2118535,Human_Splice_Rec_2118546,Human_Splice_Rec_2118547,Human_Splice_Rec_2118580,Human_Splice_Rec_2118581,Human_Splice_Rec_2118586,Human_Splice_Rec_2118587,Human_Splice_Rec_2118590,Human_Splice_Rec_2118591,Human_Splice_Rec_2118594,Human_Splice_Rec_2118595 Human_miRNA_ID_2056832,Human_miRNA_ID_2247848 RMVar_hsa_circ_98009,RMVar_hsa_circ_211953,RMVar_hsa_circ_70601 95613 RMVar_ID_95613 Human_SNP_ID_693732291 m1A Human chr21 - 33915654 33915654 33915654 CCTGGGATGACCGGTACCAAACCTCGAGCACCAGGGTGCGATGCTTCGGCTGGGGAAGTCTGGCA CCTGGGATGACCGGTACCAAACCTCGAGCACCGGGGTGCGATGCTTCGGCTGGGGAAGTCTGGCA T C AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33915650..33915739 26863196 MeRIP-seq:(Medium) rs947601107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927455,Human_RBP_ID_14267100 Human_Splice_Rec_2118589 95614 RMVar_ID_95614 Human_SNP_ID_693770650 m1A Human chr21 - 34073627 34073626 34073628 CCCGGGACGCGAAGGGGCGGGACGGCGGGGACAGTGGGGACCTAGAAACTGCTGCGCCGGACGGC CCCGGGACGCGAAGGGGCGGGACGGCGGGGA__GTGGGGACCTAGAAACTGCTGCGCCGGACGGC CTG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:34073576..34073764 26863196 MeRIP-seq:(Medium) rs1410271807 Functional Loss DEL dbSNP153 32..33 33 - - - 95615 RMVar_ID_95615 Human_SNP_ID_693770651 m1A Human chr21 - 34073629 34073629 34073629 TTCCCGGGACGCGAAGGGGCGGGACGGCGGGGACAGTGGGGACCTAGAAACTGCTGCGCCGGACG TTCCCGGGACGCGAAGGGGCGGGACGGCGGGGGCAGTGGGGACCTAGAAACTGCTGCGCCGGACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:34073223..34073814 26863196 MeRIP-seq:(Medium) rs918982546 Functional Loss SNV dbSNP153 33..33 33 - - - 95616 RMVar_ID_95616 Human_SNP_ID_693770662 m1A Human chr21 - 34073638 34073638 34073638 GCCAGCCGGTTCCCGGGACGCGAAGGGGCGGGACGGCGGGGACAGTGGGGACCTAGAAACTGCTG GCCAGCCGGTTCCCGGGACGCGAAGGGGCGGGGCGGCGGGGACAGTGGGGACCTAGAAACTGCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:34073223..34073837;chr21:34073223..34073795 26863196 MeRIP-seq:(Medium) rs1569410291 Functional Loss SNV dbSNP153 33..33 33 - - - 95617 RMVar_ID_95617 Human_SNP_ID_693818050 m1A Human chr21 + 34268624 34268624 34268624 GCGTCTGGATGGTTGAGTCTCGCCGGGCAGAGAAAGTGAAGCAAACGCATCCCTGGAAGAAGAGA GCGTCTGGATGGTTGAGTCTCGCCGGGCAGAGCAAGTGAAGCAAACGCATCCCTGGAAGAAGAGA A C AP000317.1,AP000317.2 Ensembl:ENSG00000214955,Ensembl:ENSG00000272657 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34268602..34268676 26863196 MeRIP-seq:(Medium) rs796797483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301806,RMVar_hsa_circ_211967 95618 RMVar_ID_95618 Human_SNP_ID_693818051 m1A Human chr21 + 34268624 34268624 34268624 GCGTCTGGATGGTTGAGTCTCGCCGGGCAGAGAAAGTGAAGCAAACGCATCCCTGGAAGAAGAGA GCGTCTGGATGGTTGAGTCTCGCCGGGCAGAGGAAGTGAAGCAAACGCATCCCTGGAAGAAGAGA A G AP000317.1,AP000317.2 Ensembl:ENSG00000214955,Ensembl:ENSG00000272657 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34268602..34268676 26863196 MeRIP-seq:(Medium) rs796797483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301806,RMVar_hsa_circ_211967 95619 RMVar_ID_95619 Human_SNP_ID_693846965 m1A Human chr21 + 34402714 34402714 34402714 GATGTGGGTGTAAATATGCTTATGTATGCAATATGCTTATATTTTAACGCATAAACAACATGAAT GATGTGGGTGTAAATATGCTTATGTATGCAATGTGCTTATATTTTAACGCATAAACAACATGAAT A G SMIM11A Ensembl:ENSG00000205670 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_571778,Human_RBP_ID_1603831 Human_miRNA_ID_685795,Human_miRNA_ID_685796,Human_miRNA_ID_888343,Human_miRNA_ID_888344,Human_miRNA_ID_1064978,Human_miRNA_ID_1064979,Human_miRNA_ID_1076296,Human_miRNA_ID_1076297 GWAS_ID_12600,GWAS_ID_12601,GWAS_ID_12602,GWAS_ID_12603,GWAS_ID_12604,GWAS_ID_12605,GWAS_ID_12606,GWAS_ID_12607,GWAS_ID_12608 95620 RMVar_ID_95620 Human_SNP_ID_693865927 m1A Human chr21 - 34518175 34518175 34518175 GGTCCATGTATGTGAGAGTGATCAAGAGAAGGAGGAAGAAGAGGAAATGGAAAGAATGAGGAGAC GGTCCATGTATGTGAGAGTGATCAAGAGAAGGGGGAAGAAGAGGAAATGGAAAGAATGAGGAGAC T C RCAN1 Ensembl:ENSG00000159200 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:34518126..34518227 32194978 MeRIP-seq:(Medium) rs1378151518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7042414 Human_Splice_Rec_2118858,Human_Splice_Rec_2118864,Human_Splice_Rec_2118870,Human_Splice_Rec_2118876,Human_Splice_Rec_2118880,Human_Splice_Rec_2118888,Human_Splice_Rec_2118894,Human_Splice_Rec_2118900,Human_Splice_Rec_2118906,Human_Splice_Rec_2118912 95621 RMVar_ID_95621 Human_SNP_ID_693888577 m1A Human chr21 + 34614929 34614929 34614929 CCCCCGAGAGGGGCGCGAAGGGCCGCAGCGTCACCCCGGGCCGCGCTCGCGCCTCGGCCGCCTCC CCCCCGAGAGGGGCGCGAAGGGCCGCAGCGTCCCCCCGGGCCGCGCTCGCGCCTCGGCCGCCTCC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:34614842..34615032 26863196 MeRIP-seq:(Medium) rs1001360246 Functional Loss SNV dbSNP153 33..33 33 - - - 95622 RMVar_ID_95622 Human_SNP_ID_693933155 m1A Human chr21 - 34791864 34791864 34791864 GGCGACGCACCTCGAGGGTGTCCGCCGGCCCCAGCACCCAGGGGACGCGCTGGAAAGCAAACAGG GGCGACGCACCTCGAGGGTGTCCGCCGGCCCCGGCACCCAGGGGACGCGCTGGAAAGCAAACAGG T C RUNX1 Ensembl:ENSG00000159216 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:34791813..34791917 32194978 MeRIP-seq:(Medium) rs1440151634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2437388,Human_miRNA_ID_2686530 RMVar_hsa_circ_211970,RMVar_hsa_circ_105995,RMVar_hsa_circ_126508,RMVar_hsa_circ_76660,RMVar_hsa_circ_211971,RMVar_hsa_circ_211969 95623 RMVar_ID_95623 Human_SNP_ID_693933433 m1A Human chr21 - 34792387 34792387 34792387 GGCTCGTCGCAAGCGCAGGGAGGCCCGTTCCAAGCCAGCTCGCCCTCCTACCACCTGTACTACGG GGCTCGTCGCAAGCGCAGGGAGGCCCGTTCCATGCCAGCTCGCCCTCCTACCACCTGTACTACGG T A RUNX1 Ensembl:ENSG00000159216 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:34792226..34792400 26863196 MeRIP-seq:(Medium) rs1176713877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211970,RMVar_hsa_circ_105995,RMVar_hsa_circ_126508,RMVar_hsa_circ_76660,RMVar_hsa_circ_211971,RMVar_hsa_circ_211969 95624 RMVar_ID_95624 Human_SNP_ID_693935151 m1A Human chr21 - 34799272 34799272 34799272 TCAAGTAAGCCACTTGAAAACACATTCTTTGCAGCTGAGCTGGGGTGGAAGGTCCAGGAGACTAG TCAAGTAAGCCACTTGAAAACACATTCTTTGCGGCTGAGCTGGGGTGGAAGGTCCAGGAGACTAG T C RUNX1 Ensembl:ENSG00000159216 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34799267..34799391 26863196 MeRIP-seq:(Medium) rs1394946568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927456,Human_RBP_ID_5386209,Human_RBP_ID_19110668 RMVar_hsa_circ_211970,RMVar_hsa_circ_105995,RMVar_hsa_circ_76660,RMVar_hsa_circ_211971 95625 RMVar_ID_95625 Human_SNP_ID_693943047 m1A Human chr21 + 34834523 34834523 34834523 GGTGTGGGCTGACCCTCATGGCTGTGCGCCGCAGCTGCTCCAGTTCACTGAGCCGCTCGGAAAAG GGTGTGGGCTGACCCTCATGGCTGTGCGCCGCGGCTGCTCCAGTTCACTGAGCCGCTCGGAAAAG A G RUNX1 RNACentral:URS00003C5339 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34834473..34834630 26863196 MeRIP-seq:(Medium) rs1408720761 Functional Loss SNV dbSNP153 33..33 33 - - - 95626 RMVar_ID_95626 Human_SNP_ID_693957018 m1A Human chr21 - 34888175 34888173 34888176 GCTAACCGGCGGGTGCTGGGCGACGGTGGAGGAGTATCGTCTCGCTGCTGCCCGAGTCAGGGCTG GCTAACCGGCGGGTGCTGGGCGACGGTGGAG___TATCGTCTCGCTGCTGCCCGAGTCAGGGCTG ACTC A RUNX1 Ensembl:ENSG00000159216 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:34888126..34888300 32194978 MeRIP-seq:(Medium) rs1009068762 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_151368 RMVar_hsa_circ_21683,RMVar_hsa_circ_58817,RMVar_hsa_circ_47777 95627 RMVar_ID_95627 Human_SNP_ID_693957020 m1A Human chr21 - 34888175 34888175 34888175 GCTAACCGGCGGGTGCTGGGCGACGGTGGAGGAGTATCGTCTCGCTGCTGCCCGAGTCAGGGCTG GCTAACCGGCGGGTGCTGGGCGACGGTGGAGGTGTATCGTCTCGCTGCTGCCCGAGTCAGGGCTG T A RUNX1 Ensembl:ENSG00000159216 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:34888126..34888300 32194978 MeRIP-seq:(Medium) rs538658822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151368 RMVar_hsa_circ_21683,RMVar_hsa_circ_58817,RMVar_hsa_circ_47777 95628 RMVar_ID_95628 Human_SNP_ID_693957125 m1A Human chr21 + 34888551 34888551 34888551 AAAAAAAGGAAGGTCCAACGCAGGCCAAGGAGAAGCAGCAGAGGTTGACTTCCTTCTGGCGTCCC AAAAAAAGGAAGGTCCAACGCAGGCCAAGGAGCAGCAGCAGAGGTTGACTTCCTTCTGGCGTCCC A C RUNX1 RNACentral:URS00003C5339 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34888501..34888670 26863196 MeRIP-seq:(Medium) rs753753429 Functional Loss SNV dbSNP153 33..33 33 - - - 95629 RMVar_ID_95629 Human_SNP_ID_693957126 m1A Human chr21 + 34888551 34888551 34888551 AAAAAAAGGAAGGTCCAACGCAGGCCAAGGAGAAGCAGCAGAGGTTGACTTCCTTCTGGCGTCCC AAAAAAAGGAAGGTCCAACGCAGGCCAAGGAGTAGCAGCAGAGGTTGACTTCCTTCTGGCGTCCC A T RUNX1 RNACentral:URS00003C5339 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34888501..34888670 26863196 MeRIP-seq:(Medium) rs753753429 Functional Loss SNV dbSNP153 33..33 33 - - - 95630 RMVar_ID_95630 Human_SNP_ID_693957532 m1A Human chr21 + 34889436 34889436 34889436 CCGGGCCGCGGCTCGATCCCTCCGCGCGTCTCACTTGCTGCGTGCGTCAGCGGCCAGCGAAGAGT CCGGGCCGCGGCTCGATCCCTCCGCGCGTCTCTCTTGCTGCGTGCGTCAGCGGCCAGCGAAGAGT A T RUNX1 RNACentral:URS00003C5339 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:34889406..34889506 32194978 MeRIP-seq:(Medium) rs1345686408 Functional Loss SNV dbSNP153 33..33 33 - - - 95631 RMVar_ID_95631 Human_SNP_ID_693957671 m1A Human chr21 - 34889717 34889717 34889717 AGCTCCGCGAAAATGCCCGCAGCACCGCGGGGACCGGCGCAGGGGGAAGCGGCCGCCCGCACGCG AGCTCCGCGAAAATGCCCGCAGCACCGCGGGGTCCGGCGCAGGGGGAAGCGGCCGCCCGCACGCG T A RUNX1 Ensembl:ENSG00000159216 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:34889668..34889852 26863196 MeRIP-seq:(Medium) rs544550393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22602479 Human_Splice_Rec_2119039 RMVar_hsa_circ_21683,RMVar_hsa_circ_58817,RMVar_hsa_circ_47777 95632 RMVar_ID_95632 Human_SNP_ID_694244460 m1A Human chr21 - 36070198 36070198 36070198 CCCGCGCCGTGAGCACCACGTCCCCCGAGAACAGCCGGCACAGGTCGCGCACGATGGCCAAGCCG CCCGCGCCGTGAGCACCACGTCCCCCGAGAACGGCCGGCACAGGTCGCGCACGATGGCCAAGCCG T C SETD4,AP000688.1 Ensembl:ENSG00000185917,Ensembl:ENSG00000230212 Protein coding,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:36070001..36070347;chr21:36069976..36070329;chr21:36069976..36070318 26863196 MeRIP-seq:(Medium) rs1190579111 Functional Loss SNV dbSNP153 33..33 33 - - - 95633 RMVar_ID_95633 Human_SNP_ID_694245300 m1A Human chr21 - 36072573 36072573 36072573 TTCTGGTGCACTCCCTTCTTTGTATCCTCCACAAACTTGTTCATGAGCCCCACCAGCTCCTCCTC TTCTGGTGCACTCCCTTCTTTGTATCCTCCACCAACTTGTTCATGAGCCCCACCAGCTCCTCCTC T G SETD4,AP000688.1 Ensembl:ENSG00000185917,Ensembl:ENSG00000230212 Protein coding,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:36072451..36072625 32194978 MeRIP-seq:(Medium) rs764197380 Functional Loss SNV dbSNP153 33..33 33 - - - 95634 RMVar_ID_95634 Human_SNP_ID_694245374 m1A Human chr21 - 36072752 36072752 36072752 CTTCTGGGCTCTTGGTGGCCTTGGGTCCCGCCATGTCAGTTCTCACCCACCCTGGGCAGCAGGCA CTTCTGGGCTCTTGGTGGCCTTGGGTCCCGCCGTGTCAGTTCTCACCCACCCTGGGCAGCAGGCA T C SETD4,AP000688.1 Ensembl:ENSG00000185917,Ensembl:ENSG00000230212 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:36072507..36072846;chr21:36072530..36072875;chr21:36072528..36072832 26863196 MeRIP-seq:(Medium) rs762932134 Functional Loss SNV dbSNP153 33..33 33 - - - 95635 RMVar_ID_95635 Human_SNP_ID_694294227 m1A Human chr21 - 36257705 36257702 36257706 ACATCTATCTACCTACCTACCTACCTACATCCATCTCTCTACCTACCTACCTACATCTACCTACC ACATCTATCTACCTACCTACCTACCTACATC____TCTCTACCTACCTACCTACATCTACCTACC AGATG A CBR3-AS1,CBR3-AS1:2 RNACentral:URS00009B5C87,RNACentral:URS00008BFA9E lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:36257676..36257755 26863196 MeRIP-seq:(Medium) rs1314608774 Functional Loss DEL dbSNP153 32..35 33 - - - 95636 RMVar_ID_95636 Human_SNP_ID_694311510 m1A Human chr21 + 36320298 36320298 36320298 TGGCGGCGCAGCCACCCCGCGGGATACGCCTCAGCGCGGTGAGCAGCCGCGAGGGGTGGAGCGGG TGGCGGCGCAGCCACCCCGCGGGATACGCCTCTGCGCGGTGAGCAGCCGCGAGGGGTGGAGCGGG A T MORC3 Ensembl:ENSG00000159256 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:36320248..36320378 26863196 MeRIP-seq:(Medium) rs1453744472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4679912,Human_RBP_ID_8860714,Human_RBP_ID_18423587,Human_RBP_ID_26789044,Human_RBP_ID_27820913 Human_Splice_Rec_2119535,Human_Splice_Rec_2119541,Human_Splice_Rec_2119571 RMVar_hsa_circ_212031,RMVar_hsa_circ_212032,RMVar_hsa_circ_122315,RMVar_hsa_circ_212041 95637 RMVar_ID_95637 Human_SNP_ID_694325091 m1A Human chr21 + 36369300 36369300 36369300 CAGGGAAATACTGCAGCTACCCAGACTGAAGTACCAAGTTTAGTTGTTAAAAAAGAAGAAACTGT CAGGGAAATACTGCAGCTACCCAGACTGAAGTTCCAAGTTTAGTTGTTAAAAAAGAAGAAACTGT A T MORC3 Ensembl:ENSG00000159256 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:36369253..36369333 32194978 MeRIP-seq:(Medium) rs768294365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64081 RMVar_hsa_circ_321448,RMVar_hsa_circ_212047,RMVar_hsa_circ_122779,RMVar_hsa_circ_99382,RMVar_hsa_circ_212058,RMVar_hsa_circ_212059,RMVar_hsa_circ_41839,RMVar_hsa_circ_338713,RMVar_hsa_circ_364611,RMVar_hsa_circ_212071,RMVar_hsa_circ_212074,RMVar_hsa_circ_304978,RMVar_hsa_circ_296802,RMVar_hsa_circ_212077,RMVar_hsa_circ_321504,RMVar_hsa_circ_212073,RMVar_hsa_circ_316582,RMVar_hsa_circ_212078,RMVar_hsa_circ_324964,RMVar_hsa_circ_212076,RMVar_hsa_circ_313035 95638 RMVar_ID_95638 Human_SNP_ID_694337174 m1A Human chr21 + 36413097 36413097 36413097 CCGGTAGAGGGAACCCCTGCCAGCAGAACCCAAGACCCCAGCAGCCCCGGCACGACTCCCCCTCA CCGGTAGAGGGAACCCCTGCCAGCAGAACCCATGACCCCAGCAGCCCCGGCACGACTCCCCCTCA A T CHAF1B Ensembl:ENSG00000159259 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:36413047..36413195 26863196 MeRIP-seq:(Medium) rs767663024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26344329,Human_RBP_ID_27820680 RMVar_hsa_circ_267686,RMVar_hsa_circ_11578,RMVar_hsa_circ_314336,RMVar_hsa_circ_361344,RMVar_hsa_circ_212090 95639 RMVar_ID_95639 Human_SNP_ID_694337188 m1A Human chr21 - 36413121 36413121 36413121 GTTGGGGCTGGGGCCTGTCTGGCCTGAGGGGGAGTCGTGCCGGGGCTGCTGGGGTCTTGGGTTCT GTTGGGGCTGGGGCCTGTCTGGCCTGAGGGGGTGTCGTGCCGGGGCTGCTGGGGTCTTGGGTTCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:36413070..36413270 32194978 MeRIP-seq:(Medium) rs1010287406 Functional Loss SNV dbSNP153 33..33 33 - - - 95640 RMVar_ID_95640 Human_SNP_ID_694410401 m1A Human chr21 + 36698673 36698673 36698673 CCCTTTTCAGCTCTTGGACCTGCAACACCGGGAGGGCGAGGACGCGGGACCAGCGCACCCTCGGA CCCTTTTCAGCTCTTGGACCTGCAACACCGGGTGGGCGAGGACGCGGGACCAGCGCACCCTCGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:36698624..36698924 26863196 MeRIP-seq:(Medium) rs1176378084 Functional Loss SNV dbSNP153 33..33 33 - - - 95641 RMVar_ID_95641 Human_SNP_ID_694413435 m1A Human chr21 + 36708177 36708176 36708177 CAGCCACGGCGCTTAGTGGAGGGTCTGCGGCCAGGCTCCCGGCGGAAAGATTCCGGGGAGGGCTC CAGCCACGGCGCTTAGTGGAGGGTCTGCGGCC_GGCTCCCGGCGGAAAGATTCCGGGGAGGGCTC CA C SIM2 Ensembl:ENSG00000159263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:36708176..36708304 26863196 MeRIP-seq:(Medium) rs1243973147 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5503998 95642 RMVar_ID_95642 Human_SNP_ID_694423142 m1A Human chr21 - 36744737 36744737 36744737 CTGGCCGCATTCCAGTTTGTCCATTTGGAACGAGCTGTATTGCTGCATGGCAAAGAAGATGGATG CTGGCCGCATTCCAGTTTGTCCATTTGGAACGGGCTGTATTGCTGCATGGCAAAGAAGATGGATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:36744731..36744844 26863196 MeRIP-seq:(Medium) rs774911548 Functional Loss SNV dbSNP153 33..33 33 - - - 95643 RMVar_ID_95643 Human_SNP_ID_694459779 m1A Human chr21 + 36894984 36894984 36894984 GACAGCGTGTGGTGAAGCCCAGCCCTCTGCGGATGTGCGGGAGCCTCAGCCTGTCCGCACTCTCA GACAGCGTGTGGTGAAGCCCAGCCCTCTGCGGCTGTGCGGGAGCCTCAGCCTGTCCGCACTCTCA A C RF00017-2012 RNACentral:URS000097430A SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:36894979..36895142 26863196 MeRIP-seq:(Medium) rs967826879 Functional Loss SNV dbSNP153 33..33 33 - - - 95644 RMVar_ID_95644 Human_SNP_ID_694477498 m1A Human chr21 + 36966526 36966523 36966526 GGGCGCCCGGGGGCTGCGCGGCCGCGCCGCAGAAGGTGAAGGAACAGCGCGAGGCACGCAGCCGC GGGCGCCCGGGGGCTGCGCGGCCGCGCCGC___AGGTGAAGGAACAGCGCGAGGCACGCAGCCGC CAGA C AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:36966478..36980389;chr21:36966478..36966628 26863196 MeRIP-seq:(Medium) rs931607074 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_2119895,Human_Splice_Rec_2119897,Human_Splice_Rec_2119903 95645 RMVar_ID_95645 Human_SNP_ID_694477503 m1A Human chr21 + 36966539 36966539 36966539 CTGCGCGGCCGCGCCGCAGAAGGTGAAGGAACAGCGCGAGGCACGCAGCCGCCGCACCGTGGCGC CTGCGCGGCCGCGCCGCAGAAGGTGAAGGAACGGCGCGAGGCACGCAGCCGCCGCACCGTGGCGC A G AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr21:36966491..36968582;chr21:36966488..36968660 26863196 MeRIP-seq:(Medium) rs985806315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2119895,Human_Splice_Rec_2119897,Human_Splice_Rec_2119903 95646 RMVar_ID_95646 Human_SNP_ID_694504446 m1A Human chr21 - 37072570 37072570 37072570 GGCGAGAATGGATCAATGGTGCCACGGAGCACATCGCTGACGCTGATTGTGTTCCTTTTCCACAG GGCGAGAATGGATCAATGGTGCCACGGAGCACGTCGCTGACGCTGATTGTGTTCCTTTTCCACAG T C PIGP Ensembl:ENSG00000185808 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:37072564..37072674 26863196 MeRIP-seq:(Medium) rs753966243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_208909,Human_RBP_ID_22550196,Human_RBP_ID_22744059 95647 RMVar_ID_95647 Human_SNP_ID_694504664 m1A Human chr21 - 37072982 37072982 37072982 GAACTCAGCGCTGAGGTGGCCGAGGTGTCGGGAGGGGCCTGGGTGGGCGTATGAAGGACCCGAGG GAACTCAGCGCTGAGGTGGCCGAGGTGTCGGGGGGGGCCTGGGTGGGCGTATGAAGGACCCGAGG T C PIGP Ensembl:ENSG00000185808 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:37072980..37073107 26863196 MeRIP-seq:(Medium) rs938924898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927720,Human_RBP_ID_18423357 95648 RMVar_ID_95648 Human_SNP_ID_694504695 m1A Human chr21 - 37073045 37073045 37073045 CTAGGCCTTTCCCTCAGGTTTTCCTCTTCCCCACTGCGGCTCCCCAGTCGGCGCTTGCGCGGAGA CTAGGCCTTTCCCTCAGGTTTTCCTCTTCCCCCCTGCGGCTCCCCAGTCGGCGCTTGCGCGGAGA T G PIGP Ensembl:ENSG00000185808 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:37072963..37073114 26863196 MeRIP-seq:(Medium) rs1262031161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4671705,Human_RBP_ID_5472475,Human_RBP_ID_5504002 Human_Splice_Rec_2119925,Human_Splice_Rec_2119951,Human_Splice_Rec_2119959 95649 RMVar_ID_95649 Human_SNP_ID_694507562 m1A Human chr21 - 37083230 37083230 37083230 ACAACACACAACCTAGAAGCCAGTCATACCCAACTGCTTGTCCTTCCTAAACAAAACTTATTCTG ACAACACACAACCTAGAAGCCAGTCATACCCACCTGCTTGTCCTTCCTAAACAAAACTTATTCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:37083226..37083351 26863196 MeRIP-seq:(Medium) rs556441480 Functional Loss SNV dbSNP153 33..33 33 - - - 95650 RMVar_ID_95650 Human_SNP_ID_694532469 m1A Human chr21 - 37182789 37182789 37182789 TTCTCTTTCCAAATCTTGAAGGAACCAATCTAATTCCGTCTTTGAGATCTAAAAACATTTAGAAA TTCTCTTTCCAAATCTTGAAGGAACCAATCTATTTCCGTCTTTGAGATCTAAAAACATTTAGAAA T A L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:37182778..37182879 32194978 MeRIP-seq:(Medium) rs756744492 Functional Loss SNV dbSNP153 33..33 33 - - - 95651 RMVar_ID_95651 Human_SNP_ID_694537245 m1A Human chr21 + 37201883 37201883 37201883 AAAGTACTATGAACGTCTCGAAGCAGTATTCTAGTGATAAGAATTCTTAACATAGCCAAGCGCCC AAAGTACTATGAACGTCTCGAAGCAGTATTCTGGTGATAAGAATTCTTAACATAGCCAAGCGCCC A G TTC3 Ensembl:ENSG00000182670 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:37201751..37201950 26863410 MeRIP-seq:(Medium) rs1401041174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572234,Human_RBP_ID_14289048,Human_RBP_ID_23926583 Human_miRNA_ID_720929 RMVar_hsa_circ_111751,RMVar_hsa_circ_212157 95652 RMVar_ID_95652 Human_SNP_ID_694578615 m1A Human chr21 + 37366955 37366952 37366956 CTGCTGCTGATCGCGGCCCAGGTCGGCCTCAGAGAGCGGACACCCCGAGCGGGGGGTGCGGGCGC CTGCTGCTGATCGCGGCCCAGGTCGGCCTC____AGCGGACACCCCGAGCGGGGGGTGCGGGCGC CAGAG C DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:37366857..37367075;chr21:37366905..37367052 26863196 MeRIP-seq:(Medium) rs1012520804 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5652765,Human_RBP_ID_14290091,Human_RBP_ID_18423359,Human_RBP_ID_18496106 95653 RMVar_ID_95653 Human_SNP_ID_694578616 m1A Human chr21 + 37366955 37366952 37366956 CTGCTGCTGATCGCGGCCCAGGTCGGCCTCAGAGAGCGGACACCCCGAGCGGGGGGTGCGGGCGC CTGCTGCTGATCGCGGCCCAGGTCGGCCTCAG__AGCGGACACCCCGAGCGGGGGGTGCGGGCGC CAGAG CAG DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:37366857..37367075;chr21:37366905..37367052 26863196 MeRIP-seq:(Medium) rs1012520804 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5652765,Human_RBP_ID_14290091,Human_RBP_ID_18423359,Human_RBP_ID_18496106 95654 RMVar_ID_95654 Human_SNP_ID_694578692 m1A Human chr21 + 37367122 37367111 37367123 AGGGAGCGTGTGCGAGGGCGATTGTGCGCGCGAGTGTGCGGGTGTGTGCGAGTGTCTGTCTGTCT AGGGAGCGTGTGCGAGGGCGAT____________TGTGCGGGTGTGTGCGAGTGTCTGTCTGTCT TTGTGCGCGCGAG T DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:37366008..37410575;chr21:37366065..37410575 26863196 MeRIP-seq:(Medium) rs1260032743 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_64677,Human_RBP_ID_3961239,Human_RBP_ID_4679929,Human_RBP_ID_5297559,Human_RBP_ID_5529703,Human_RBP_ID_5652769,Human_RBP_ID_9332125,Human_RBP_ID_17979616,Human_RBP_ID_18463595,Human_RBP_ID_22083576,Human_RBP_ID_23115532,Human_RBP_ID_23926671 95655 RMVar_ID_95655 Human_SNP_ID_694579443 m1A Human chr21 + 37368728 37368728 37368728 GTCTGGAGAGGGGCACTGACTGGTCTAAGGTCATACAGCTGGGACTCCAGGAGCCAGAAGGCTGT GTCTGGAGAGGGGCACTGACTGGTCTAAGGTCCTACAGCTGGGACTCCAGGAGCCAGAAGGCTGT A C DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:37368722..37368822 32194978 MeRIP-seq:(Medium) rs1422003587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832992,Human_RBP_ID_7044799,Human_RBP_ID_9122545,Human_RBP_ID_10036615,Human_RBP_ID_14290145,Human_RBP_ID_17144881 RMVar_hsa_circ_112754,RMVar_hsa_circ_212162 95656 RMVar_ID_95656 Human_SNP_ID_694582657 m1A Human chr21 + 37378988 37378988 37378988 TTGACAGTCTATTGGAGGAAGTCATGTGGGCAATGGGTGGTGGTGGGAAATGAAGGTGACTTTGA TTGACAGTCTATTGGAGGAAGTCATGTGGGCAGTGGGTGGTGGTGGGAAATGAAGGTGACTTTGA A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:37378983..37379296 26863196 MeRIP-seq:(Medium) rs79787072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7044934,Human_RBP_ID_23926744 RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 95657 RMVar_ID_95657 Human_SNP_ID_694592171 m1A Human chr21 + 37412693 37412693 37412693 TGAGGCACTTCGAAAATGGATAGGATTTAGTAAGACCATTTAGATAAAGTCAGCAGCTTCTAATG TGAGGCACTTCGAAAATGGATAGGATTTAGTACGACCATTTAGATAAAGTCAGCAGCTTCTAATG A C DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:37412691..37413078 26863196 MeRIP-seq:(Medium) rs1273737882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14293550 RMVar_hsa_circ_5942,RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 95658 RMVar_ID_95658 Human_SNP_ID_694592183 m1A Human chr21 + 37412754 37412754 37412754 AATGAAATTACTGAAAGAATGGTGGTGCGGGAATAGAGATGGGAAGTTCAAGTGGATAACATGTG AATGAAATTACTGAAAGAATGGTGGTGCGGGATTAGAGATGGGAAGTTCAAGTGGATAACATGTG A T DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:37412749..37413006 26863196 MeRIP-seq:(Medium) rs770857107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7045427,Human_RBP_ID_14293564 RMVar_hsa_circ_5942,RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 95659 RMVar_ID_95659 Human_SNP_ID_694592202 m1A Human chr21 + 37412823 37412823 37412823 AGGAATGTGATGAGGAGTTGTAGGCATAGAGAATGGAGGCAGGGATGTGGCACTGTAGGCAGCCA AGGAATGTGATGAGGAGTTGTAGGCATAGAGAGTGGAGGCAGGGATGTGGCACTGTAGGCAGCCA A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:37412818..37413005 26863196 MeRIP-seq:(Medium) rs555895151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14293567 RMVar_hsa_circ_5942,RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 95660 RMVar_ID_95660 Human_SNP_ID_694600746 m1A Human chr21 + 37444747 37444747 37444747 GTGGGTAGGGGATGATAAATTAGTTTGCTTCTAGATAAGATGAGTAGAACATCTAAGTAGAAAAT GTGGGTAGGGGATGATAAATTAGTTTGCTTCTGGATAAGATGAGTAGAACATCTAAGTAGAAAAT A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:37444738..37444837 26863196 MeRIP-seq:(Medium) rs1226854137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14295570,Human_RBP_ID_22602537 RMVar_hsa_circ_212168,RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_124984,RMVar_hsa_circ_272668,RMVar_hsa_circ_304262,RMVar_hsa_circ_268296,RMVar_hsa_circ_374595,RMVar_hsa_circ_307716,RMVar_hsa_circ_274534,RMVar_hsa_circ_271671,RMVar_hsa_circ_271987,RMVar_hsa_circ_27672,RMVar_hsa_circ_212172,RMVar_hsa_circ_212173,RMVar_hsa_circ_212170,RMVar_hsa_circ_212171,RMVar_hsa_circ_212169,RMVar_hsa_circ_212167 95661 RMVar_ID_95661 Human_SNP_ID_694603926 m1A Human chr21 - 37456202 37456202 37456202 CTCTCAAGTACACTCTTCACTCTTCCCCAAACATGATTCCCCTACTGCTCTGCCTAACTCCCACT CTCTCAAGTACACTCTTCACTCTTCCCCAAACTTGATTCCCCTACTGCTCTGCCTAACTCCCACT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:37456194..37456289 26863196 MeRIP-seq:(Medium) rs1027403893 Functional Loss SNV dbSNP153 33..33 33 - - - 95662 RMVar_ID_95662 Human_SNP_ID_694620427 m1A Human chr21 + 37514879 37514879 37514879 TCTGTGCTGGTTGCCACATCTTAGCAAGCACCAAAAAACTAAAGCAGTTTTTAAACCGATATTTA TCTGTGCTGGTTGCCACATCTTAGCAAGCACCCAAAAACTAAAGCAGTTTTTAAACCGATATTTA A C DYRK1A Ensembl:ENSG00000157540 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1229587779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17284206,Human_RBP_ID_26496131,Human_RBP_ID_27705859 Human_miRNA_ID_184469 95663 RMVar_ID_95663 Human_SNP_ID_694894942 m1A Human chr21 - 38660942 38660942 38660942 GTCCTAAACCCGAGCAGGGCGCGTAGTGTCCAAACCTGCCCGCGCGGCCCGCGCTCTTGGCCCCG GTCCTAAACCCGAGCAGGGCGCGTAGTGTCCACACCTGCCCGCGCGGCCCGCGCTCTTGGCCCCG T G ERG Ensembl:ENSG00000157554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr21:38660783..38660969;chr21:38660817..38660955 26863196 MeRIP-seq:(Medium) rs1047621639 Functional Loss SNV dbSNP153 33..33 33 - - - 95664 RMVar_ID_95664 Human_SNP_ID_694930992 m1A Human chr21 + 38805974 38805974 38805974 AGAGACTGACGAGTGCGGTGTCGCTCCAGCTCAGAGCTCCCGGAGCCGCCCGGCCAGCGTCCGGC AGAGACTGACGAGTGCGGTGTCGCTCCAGCTCCGAGCTCCCGGAGCCGCCCGGCCAGCGTCCGGC A C ETS2 Ensembl:ENSG00000157557 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:38805855..38806783 26863196 MeRIP-seq:(Medium) rs1250553338 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4679735,Human_RBP_ID_5132839,Human_RBP_ID_9432080,Human_RBP_ID_17572565,Human_RBP_ID_22453976 Human_Splice_Rec_2121894 RMVar_hsa_circ_212194,RMVar_hsa_circ_126433 95665 RMVar_ID_95665 Human_SNP_ID_694930993 m1A Human chr21 + 38805974 38805974 38805974 AGAGACTGACGAGTGCGGTGTCGCTCCAGCTCAGAGCTCCCGGAGCCGCCCGGCCAGCGTCCGGC AGAGACTGACGAGTGCGGTGTCGCTCCAGCTCTGAGCTCCCGGAGCCGCCCGGCCAGCGTCCGGC A T ETS2 Ensembl:ENSG00000157557 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:38805855..38806783 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4679735,Human_RBP_ID_5132839,Human_RBP_ID_9432080,Human_RBP_ID_17572565,Human_RBP_ID_22453976 Human_Splice_Rec_2121894 RMVar_hsa_circ_212194,RMVar_hsa_circ_126433 95666 RMVar_ID_95666 Human_SNP_ID_694931073 m1A Human chr21 + 38806138 38806138 38806138 GCCCGCAGCGGCAGGGTAAGAGCTGGGCCCGCAGAGAGCGCCCGGCGCGCGGCTCCAGTCCCATG GCCCGCAGCGGCAGGGTAAGAGCTGGGCCCGCGGAGAGCGCCCGGCGCGCGGCTCCAGTCCCATG A G ETS2 Ensembl:ENSG00000157557 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:38806130..38806747 26863196 MeRIP-seq:(Medium) rs142089113 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_928122,Human_RBP_ID_19110719,Human_RBP_ID_26789058 RMVar_hsa_circ_212194,RMVar_hsa_circ_126433 95667 RMVar_ID_95667 Human_SNP_ID_694933281 m1A Human chr21 + 38815835 38815835 38815835 AGTGGCACATGCCTGTAATCCCAGATACTCGGAAGCCTGAGGCAGGAGAATCCCTTGAGCCCGGG AGTGGCACATGCCTGTAATCCCAGATACTCGGGAGCCTGAGGCAGGAGAATCCCTTGAGCCCGGG A G ETS2 Ensembl:ENSG00000157557 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:38815832..38815936 26863196 MeRIP-seq:(Medium) rs1569023767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212194,RMVar_hsa_circ_126433,RMVar_hsa_circ_269749,RMVar_hsa_circ_50299 95668 RMVar_ID_95668 Human_SNP_ID_694933287 m1A Human chr21 + 38815849 38815849 38815849 GTAATCCCAGATACTCGGAAGCCTGAGGCAGGAGAATCCCTTGAGCCCGGGAGGCAGAGGTTGCA GTAATCCCAGATACTCGGAAGCCTGAGGCAGGGGAATCCCTTGAGCCCGGGAGGCAGAGGTTGCA A G ETS2 Ensembl:ENSG00000157557 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:38815846..38815941 26863196 MeRIP-seq:(Medium) rs186223267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212194,RMVar_hsa_circ_126433,RMVar_hsa_circ_269749,RMVar_hsa_circ_50299 95669 RMVar_ID_95669 Human_SNP_ID_694934830 m1A Human chr21 + 38821674 38821674 38821674 TGCCAGTCATTCATCAGCTGGACTGGAGACGGATGGGAGTTTAAGCTCGCCGACCCCGATGAGGT TGCCAGTCATTCATCAGCTGGACTGGAGACGGTTGGGAGTTTAAGCTCGCCGACCCCGATGAGGT A T ETS2 Ensembl:ENSG00000157557 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:38821626..38821725 26863196 MeRIP-seq:(Medium) rs766080329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5597170,Human_RBP_ID_7046816,Human_RBP_ID_8542337,Human_RBP_ID_9391741,Human_RBP_ID_14301304,Human_RBP_ID_18326407,Human_RBP_ID_22454130 Human_Splice_Rec_2121910,Human_Splice_Rec_2121911,Human_Splice_Rec_2121934,Human_Splice_Rec_2121935,Human_Splice_Rec_2121952,Human_Splice_Rec_2121953,Human_Splice_Rec_2121982,Human_Splice_Rec_2121983,Human_Splice_Rec_2122000,Human_Splice_Rec_2122001,Human_Splice_Rec_2122018,Human_Splice_Rec_2122019 Human_miRNA_ID_2214968 RMVar_hsa_circ_124271,RMVar_hsa_circ_212194,RMVar_hsa_circ_126433,RMVar_hsa_circ_114399,RMVar_hsa_circ_212197,RMVar_hsa_circ_212198 95670 RMVar_ID_95670 Human_SNP_ID_695021145 m1A Human chr21 - 39175916 39175916 39175916 GAAGACATCTTGTGGGGAAGGTCGGGCGGGTTAGAGCATAGACTTCCTCCAGAGGCCAGGAGACC GAAGACATCTTGTGGGGAAGGTCGGGCGGGTTGGAGCATAGACTTCCTCCAGAGGCCAGGAGACC T C PSMG1 Ensembl:ENSG00000183527 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:39175871..39176005 26863196 MeRIP-seq:(Medium) rs888601462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5386777,Human_RBP_ID_7047118,Human_RBP_ID_8235192,Human_RBP_ID_14304354,Human_RBP_ID_17208477,Human_RBP_ID_20702169,Human_RBP_ID_22550402,Human_RBP_ID_22602562 RMVar_hsa_circ_212200,RMVar_hsa_circ_113415 95671 RMVar_ID_95671 Human_SNP_ID_695021528 m1A Human chr21 - 39177540 39177540 39177540 GTTCTAAGCTACTGTCAAGTATGGAAAATCCCAGCAATTCTGTACTTGTGTTATACTGATGTGAT GTTCTAAGCTACTGTCAAGTATGGAAAATCCCGGCAATTCTGTACTTGTGTTATACTGATGTGAT T C PSMG1 Ensembl:ENSG00000183527 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs14194 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_928904,Human_RBP_ID_1937081,Human_RBP_ID_18781108,Human_RBP_ID_25650385,Human_RBP_ID_26821789 Human_Splice_Rec_2122214,Human_Splice_Rec_2122218,Human_Splice_Rec_2122230,Human_Splice_Rec_2122240,Human_Splice_Rec_2122250 Human_miRNA_ID_1359235 GWAS_ID_12609,GWAS_ID_12610,GWAS_ID_12611,GWAS_ID_12612 RMVar_hsa_circ_10504,RMVar_hsa_circ_212200,RMVar_hsa_circ_113415,RMVar_hsa_circ_325090,RMVar_hsa_circ_350529 95672 RMVar_ID_95672 Human_SNP_ID_695022649 m1A Human chr21 - 39181880 39181880 39181880 AGTTGCTTTAGTTTCATCTTGTTTCTTGTGTTAGGGAAGTGCGGCTCCTTCGAAGACAAACAAAA AGTTGCTTTAGTTTCATCTTGTTTCTTGTGTTTGGGAAGTGCGGCTCCTTCGAAGACAAACAAAA T A PSMG1 Ensembl:ENSG00000183527 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr21:39181801..39181900;chr21:39181776..39183112;chr21:39181801..39181944;chr21:39181778..39183112 26863196,32194978 MeRIP-seq:(Medium) rs1555910614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4672506,Human_RBP_ID_14304731,Human_RBP_ID_25643746 95673 RMVar_ID_95673 Human_SNP_ID_695023086 m1A Human chr21 - 39183327 39183327 39183327 GGTGAAGGCGCCGTGCCGAGCTGGGACTGAGGACGAAGAGGAGGAGGAGGAGGGGCGGAGGGAGA GGTGAAGGCGCCGTGCCGAGCTGGGACTGAGGGCGAAGAGGAGGAGGAGGAGGGGCGGAGGGAGA T C PSMG1 Ensembl:ENSG00000183527 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:39183251..39183460;chr21:39183276..39183450 26863196 MeRIP-seq:(Medium) rs973547342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245520,Human_RBP_ID_780751,Human_RBP_ID_1027960,Human_RBP_ID_4672509,Human_RBP_ID_7047197,Human_RBP_ID_8942960,Human_RBP_ID_9332133,Human_RBP_ID_14304795,Human_RBP_ID_23009646,Human_RBP_ID_24547045,Human_RBP_ID_25643759,Human_RBP_ID_26495030 Human_Splice_Rec_2122205,Human_Splice_Rec_2122233,Human_Splice_Rec_2122243 95674 RMVar_ID_95674 Human_SNP_ID_695023095 m1A Human chr21 + 39183346 39183346 39183346 CTCCTCCTCTTCGTCCTCAGTCCCAGCTCGGCACGGCGCCTTCACCACCTCTCCGAAGAACGTGG CTCCTCCTCTTCGTCCTCAGTCCCAGCTCGGCCCGGCGCCTTCACCACCTCTCCGAAGAACGTGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:39183251..39183392 26863196 MeRIP-seq:(Medium) rs1239246938 Functional Loss SNV dbSNP153 33..33 33 - - - 95675 RMVar_ID_95675 Human_SNP_ID_695058736 m1A Human chr21 + 39313056 39313056 39313056 GGTCGGCAGGAGGAACCCGAGGGAGCGCGGGGACGGGCGCGCACAGACCTGGTACTGCTCCAGCT GGTCGGCAGGAGGAACCCGAGGGAGCGCGGGGGCGGGCGCGCACAGACCTGGTACTGCTCCAGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:39313052..39313137 26863196 MeRIP-seq:(Medium) rs1460800762 Functional Loss SNV dbSNP153 33..33 33 - - - 95676 RMVar_ID_95676 Human_SNP_ID_695058945 m1A Human chr21 + 39313363 39313354 39313363 CGGCGGGGAGGGGAGGGGGACGGGGCCAGGGGAGCCGGGGGAGCCCGGGGAGCCGGGGAAGCCGA CGGCGGGGAGGGGAGGGGGACGGG_________GCCGGGGGAGCCCGGGGAGCCGGGGAAGCCGA GGCCAGGGGA G BRWD1-AS1 RNACentral:URS00009BBA74 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:39313361..39313538 26863196 MeRIP-seq:(Medium) rs1358322694 Functional Loss DEL dbSNP153 25..33 33 - - - 95677 RMVar_ID_95677 Human_SNP_ID_695058951 m1A Human chr21 + 39313363 39313357 39313364 CGGCGGGGAGGGGAGGGGGACGGGGCCAGGGGAGCCGGGGGAGCCCGGGGAGCCGGGGAAGCCGA CGGCGGGGAGGGGAGGGGGACGGGGCC_______CCGGGGGAGCCCGGGGAGCCGGGGAAGCCGA CAGGGGAG C BRWD1-AS1 RNACentral:URS00009BBA74 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr21:39313361..39313538 26863196 MeRIP-seq:(Medium) rs1555880661 Functional Loss DEL dbSNP153 28..34 33 - - - 95678 RMVar_ID_95678 Human_SNP_ID_695059071 m1A Human chr21 - 39313538 39313538 39313538 CGCCAGCCCGGTCAGGCCTCGGCGCGGCCTACACGCTCCGCTCGCTCGCTCGCTCCCGCCTCCCG CGCCAGCCCGGTCAGGCCTCGGCGCGGCCTACGCGCTCCGCTCGCTCGCTCGCTCCCGCCTCCCG T C BRWD1 Ensembl:ENSG00000185658 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:39313302..39313600 26863410 MeRIP-seq:(Medium) rs1045946894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245369,Human_RBP_ID_572514,Human_RBP_ID_832999,Human_RBP_ID_4672782,Human_RBP_ID_9332135,Human_RBP_ID_26821795 Human_Splice_Rec_2122253,Human_Splice_Rec_2122385,Human_Splice_Rec_2122465,Human_Splice_Rec_2122721 RMVar_hsa_circ_108675,RMVar_hsa_circ_212248 95679 RMVar_ID_95679 Human_SNP_ID_695059572 m1A Human chr21 + 39314077 39314077 39314077 TGGGCAAGGTCGCCCGCTCCGGGTCGCTCGGAAGGGTCATTTCACGGACCGGTCGTCTGGGGCCA TGGGCAAGGTCGCCCGCTCCGGGTCGCTCGGATGGGTCATTTCACGGACCGGTCGTCTGGGGCCA A T BRWD1-AS2 Ensembl:ENSG00000255568 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:39314032..39314131 26863196 MeRIP-seq:(Medium) rs1330521278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3666358,Human_RBP_ID_17701315 95680 RMVar_ID_95680 Human_SNP_ID_695059816 m1A Human chr21 - 39314417 39314417 39314417 CACCCTCTCCCCACAGTCCCGTTTTCCTGTCCATGCTTGGATGGATCCAGCCGAGCCGTCAGCCG CACCCTCTCCCCACAGTCCCGTTTTCCTGTCCGTGCTTGGATGGATCCAGCCGAGCCGTCAGCCG T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:39314368..39314455 26863196 MeRIP-seq:(Medium) rs1195210677 Functional Loss SNV dbSNP153 33..33 33 - - - 95681 RMVar_ID_95681 Human_SNP_ID_695059821 m1A Human chr21 + 39314427 39314427 39314427 CTCGGCTGGATCCATCCAAGCATGGACAGGAAAACGGGACTGTGGGGAGAGGGTGGTGCAGACGG CTCGGCTGGATCCATCCAAGCATGGACAGGAAGACGGGACTGTGGGGAGAGGGTGGTGCAGACGG A G BRWD1-AS2 Ensembl:ENSG00000255568 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:39314376..39314506 26863196 MeRIP-seq:(Medium) rs898075732 Functional Loss SNV dbSNP153 33..33 33 - - - 95682 RMVar_ID_95682 Human_SNP_ID_695061656 m1A Human chr21 + 39321531 39321531 39321531 CCTCCAGAGGCTCCCATCAGACCCAGAGGAAAAGGCCAAGTCCACACGATCTGGCCTCTCTCTGG CCTCCAGAGGCTCCCATCAGACCCAGAGGAAAGGGCCAAGTCCACACGATCTGGCCTCTCTCTGG A G BRWD1-AS1 Ensembl:ENSG00000238141 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:39321482..39321633 26863196 MeRIP-seq:(Medium) rs1405819098 Functional Loss SNV dbSNP153 33..33 33 - - - 95683 RMVar_ID_95683 Human_SNP_ID_695069343 m1A Human chr21 - 39347868 39347868 39347868 TACAGTTTCCAAGCCAACTTCGGGAAGCCTTAACCTTTTTACGGGGTGGGGGTGGGGAGGTAAAA TACAGTTTCCAAGCCAACTTCGGGAAGCCTTACCCTTTTTACGGGGTGGGGGTGGGGAGGTAAAA T G HMGN1 Ensembl:ENSG00000205581 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:39347866..39348015 32194978 MeRIP-seq:(Medium) rs1175943940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2704340,Human_RBP_ID_7048319,Human_RBP_ID_10042607,Human_RBP_ID_14311714,Human_RBP_ID_17019908,Human_RBP_ID_23008263,Human_RBP_ID_23927897,Human_RBP_ID_25645104 Human_Splice_Rec_2122810,Human_Splice_Rec_2122944,Human_Splice_Rec_2122950 RMVar_hsa_circ_84499,RMVar_hsa_circ_212321 95684 RMVar_ID_95684 Human_SNP_ID_695069683 m1A Human chr21 - 39348579 39348566 39348579 GCCCGCCTCTATTCGTGCGTCTCCGTCTCCGCAGGTCAGCTCCGCCGAAGGCGCCGCCAAGGAAG GCCCGCCTCTATTCGTGCGTCTCCGTCTCCGC_____________CGAAGGCGCCGCCAAGGAAG GGCGGAGCTGACCT G HMGN1 Ensembl:ENSG00000205581 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr21:39348480..39348642 26863410 MeRIP-seq:(Medium) rs1295777484 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_928154,Human_RBP_ID_1604533,Human_RBP_ID_5386450,Human_RBP_ID_9391503,Human_RBP_ID_19110308,Human_RBP_ID_22479409,Human_RBP_ID_22673734,Human_RBP_ID_23009798 Human_Splice_Rec_2122747,Human_Splice_Rec_2122759,Human_Splice_Rec_2122769,Human_Splice_Rec_2122777,Human_Splice_Rec_2122791,Human_Splice_Rec_2122805,Human_Splice_Rec_2122823,Human_Splice_Rec_2122835,Human_Splice_Rec_2122843,Human_Splice_Rec_2122853,Human_Splice_Rec_2122863,Human_Splice_Rec_2122877,Human_Splice_Rec_2122885,Human_Splice_Rec_2122905,Human_Splice_Rec_2122929,Human_Splice_Rec_2122939,Human_Splice_Rec_2122945 RMVar_hsa_circ_68335 95685 RMVar_ID_95685 Human_SNP_ID_695069903 m1A Human chr21 - 39348972 39348972 39348972 CGAAGGCTGTCGGCGCGCCGCGGCCCGCAGGCACCCGGCACGCGCCTTCCCCGCAGGCACCCGGC CGAAGGCTGTCGGCGCGCCGCGGCCCGCAGGCTCCCGGCACGCGCCTTCCCCGCAGGCACCCGGC T A HMGN1 Ensembl:ENSG00000205581 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr21:39348928..39349037 26863410 MeRIP-seq:(Medium) rs1367560238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572560,Human_RBP_ID_780767,Human_RBP_ID_4679739,Human_RBP_ID_9332398,Human_RBP_ID_27027665 Human_Splice_Rec_2122745,Human_Splice_Rec_2122757,Human_Splice_Rec_2122767,Human_Splice_Rec_2122775,Human_Splice_Rec_2122803,Human_Splice_Rec_2122821,Human_Splice_Rec_2122833,Human_Splice_Rec_2122841,Human_Splice_Rec_2122903,Human_Splice_Rec_2122919,Human_Splice_Rec_2122927,Human_Splice_Rec_2122937,Human_Splice_Rec_2122951,Human_Splice_Rec_2122953 RMVar_hsa_circ_68335 95686 RMVar_ID_95686 Human_SNP_ID_695069904 m1A Human chr21 - 39348972 39348972 39348972 CGAAGGCTGTCGGCGCGCCGCGGCCCGCAGGCACCCGGCACGCGCCTTCCCCGCAGGCACCCGGC CGAAGGCTGTCGGCGCGCCGCGGCCCGCAGGCGCCCGGCACGCGCCTTCCCCGCAGGCACCCGGC T C HMGN1 Ensembl:ENSG00000205581 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr21:39348928..39349037 26863410 MeRIP-seq:(Medium) rs1367560238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572560,Human_RBP_ID_780767,Human_RBP_ID_4679739,Human_RBP_ID_9332398,Human_RBP_ID_27027665 Human_Splice_Rec_2122745,Human_Splice_Rec_2122757,Human_Splice_Rec_2122767,Human_Splice_Rec_2122775,Human_Splice_Rec_2122803,Human_Splice_Rec_2122821,Human_Splice_Rec_2122833,Human_Splice_Rec_2122841,Human_Splice_Rec_2122903,Human_Splice_Rec_2122919,Human_Splice_Rec_2122927,Human_Splice_Rec_2122937,Human_Splice_Rec_2122951,Human_Splice_Rec_2122953 RMVar_hsa_circ_68335 95687 RMVar_ID_95687 Human_SNP_ID_695069907 m1A Human chr21 - 39348976 39348976 39348976 TTCGCGAAGGCTGTCGGCGCGCCGCGGCCCGCAGGCACCCGGCACGCGCCTTCCCCGCAGGCACC TTCGCGAAGGCTGTCGGCGCGCCGCGGCCCGCTGGCACCCGGCACGCGCCTTCCCCGCAGGCACC T A HMGN1 Ensembl:ENSG00000205581 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Starvation treatment chr21:39348951..39348975;chr21:39348910..39349038 26863196,26863410 MeRIP-seq:(Medium) rs1234115651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572560,Human_RBP_ID_780767,Human_RBP_ID_4679739,Human_RBP_ID_9332398 Human_Splice_Rec_2122745,Human_Splice_Rec_2122757,Human_Splice_Rec_2122767,Human_Splice_Rec_2122775,Human_Splice_Rec_2122803,Human_Splice_Rec_2122821,Human_Splice_Rec_2122833,Human_Splice_Rec_2122841,Human_Splice_Rec_2122903,Human_Splice_Rec_2122919,Human_Splice_Rec_2122927,Human_Splice_Rec_2122937,Human_Splice_Rec_2122951,Human_Splice_Rec_2122953 RMVar_hsa_circ_68335 95688 RMVar_ID_95688 Human_SNP_ID_695069914 m1A Human chr21 + 39348997 39348997 39348997 TGCCGGGTGCCTGCGGGCCGCGGCGCGCCGACAGCCTTCGCGAAACTGGGCTGCCTTGCCGCTGC TGCCGGGTGCCTGCGGGCCGCGGCGCGCCGACGGCCTTCGCGAAACTGGGCTGCCTTGCCGCTGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:39348946..39349046 32194978 MeRIP-seq:(Medium) rs1435005468 Functional Loss SNV dbSNP153 33..33 33 - - - 95689 RMVar_ID_95689 Human_SNP_ID_695069918 m1A Human chr21 + 39349007 39349006 39349007 CTGCGGGCCGCGGCGCGCCGACAGCCTTCGCGAAACTGGGCTGCCTTGCCGCTGCCACTCCTCCC CTGCGGGCCGCGGCGCGCCGACAGCCTTCGCG_AACTGGGCTGCCTTGCCGCTGCCACTCCTCCC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:39348401..39349100;chr21:39348311..39349125 26863196 MeRIP-seq:(Medium) rs1202726207 Functional Loss DEL dbSNP153 33..33 33 - - - 95690 RMVar_ID_95690 Human_SNP_ID_695078590 m1A Human chr21 + 39380449 39380449 39380449 GTTGCTGGTGCTCAGCTTCGTGTTTGGATGCAATGTTCTTAGGATCCTCCTCCCGTCCTTCTCAT GTTGCTGGTGCTCAGCTTCGTGTTTGGATGCAGTGTTCTTAGGATCCTCCTCCCGTCCTTCTCAT A G GET1,GET1-SH3BGR Ensembl:ENSG00000182093,Ensembl:ENSG00000285815 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:39380351..39380475 26863410 MeRIP-seq:(Medium) rs899026804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_928157,Human_RBP_ID_4680115,Human_RBP_ID_9332137 Human_Splice_Rec_2122979,Human_Splice_Rec_2122987,Human_Splice_Rec_2123003,Human_Splice_Rec_2123019,Human_Splice_Rec_2123035,Human_Splice_Rec_2123039,Human_Splice_Rec_2123041,Human_Splice_Rec_2123059,Human_Splice_Rec_2123137,Human_Splice_Rec_2123153 95691 RMVar_ID_95691 Human_SNP_ID_418754428 m1A Human chr10 - 135226 135226 135226 GCCGGGTCGCCGCGTGCGGGGTGAGGGCCGGGAGGGCACCGCCGCCCGCACTTACTCGCGTCTTC GCCGGGTCGCCGCGTGCGGGGTGAGGGCCGGGTGGGCACCGCCGCCCGCACTTACTCGCGTCTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:135175..135298 26863196 MeRIP-seq:(Medium) rs1554751526 Functional Loss SNV dbSNP153 33..33 33 - - - 95692 RMVar_ID_95692 Human_SNP_ID_418773783 m1A Human chr10 - 209832 209832 209832 TAAAAATCTTTCAGTACTGAAAACTAAAAATGAATGAAAATAAGAAAATGGTGGTAATTTCTTTC TAAAAATCTTTCAGTACTGAAAACTAAAAATGGATGAAAATAAGAAAATGGTGGTAATTTCTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:209828..209911 26863196 MeRIP-seq:(Medium) rs965509772 Functional Loss SNV dbSNP153 33..33 33 - - - 95693 RMVar_ID_95693 Human_SNP_ID_418784339 m1A Human chr10 + 248988 248988 248988 CAACATGCAGGGTGAGATGGACAGAAAATGTAAGCAAGTAAAGGAAAAGTGTAAGGAAGAATTTG CAACATGCAGGGTGAGATGGACAGAAAATGTAGGCAAGTAAAGGAAAAGTGTAAGGAAGAATTTG A G ZMYND11 Ensembl:ENSG00000015171 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:248938..249126 26863196 MeRIP-seq:(Medium) rs528139884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2213245,Human_RBP_ID_18592640 Human_Splice_Rec_1105836,Human_Splice_Rec_1105860,Human_Splice_Rec_1105884,Human_Splice_Rec_1105910,Human_Splice_Rec_1105938,Human_Splice_Rec_1105964,Human_Splice_Rec_1105988,Human_Splice_Rec_1106014,Human_Splice_Rec_1106040,Human_Splice_Rec_1106062,Human_Splice_Rec_1106100,Human_Splice_Rec_1106126,Human_Splice_Rec_1106150 RMVar_hsa_circ_270536,RMVar_hsa_circ_141448,RMVar_hsa_circ_141452,RMVar_hsa_circ_336343,RMVar_hsa_circ_288166,RMVar_hsa_circ_141454,RMVar_hsa_circ_290986,RMVar_hsa_circ_359468 95694 RMVar_ID_95694 Human_SNP_ID_418785261 m1A Human chr10 + 252315 252315 252315 ATTTTAACCAGTCGCTTACACATCCACACCCAAGTCTAAAGACTGCCCCGATTTCTTACCTGCAG ATTTTAACCAGTCGCTTACACATCCACACCCACGTCTAAAGACTGCCCCGATTTCTTACCTGCAG A C ZMYND11 Ensembl:ENSG00000015171 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:252311..252500 26863196 MeRIP-seq:(Medium) rs1472346164 Functional Loss SNV dbSNP153 33..33 33 - - - 95695 RMVar_ID_95695 Human_SNP_ID_418881980 m1A Human chr10 + 525639 525639 525639 TCTGCAAGTGAAAATGAACCTCCTGCTTGCCCACTGAGGACAGGGAGAGAACAGGGTAGGATAAC TCTGCAAGTGAAAATGAACCTCCTGCTTGCCCCCTGAGGACAGGGAGAGAACAGGGTAGGATAAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:525637..525793 32194978 MeRIP-seq:(Medium) rs1011985474 Functional Loss SNV dbSNP153 33..33 33 - - - 95696 RMVar_ID_95696 Human_SNP_ID_418893149 m1A Human chr10 + 554506 554504 554506 TACATCACTGTCAAGGGTGGTTATAAGTTATAAAATAACTTAAATACTTCACAAAACCTTGGGCT TACATCACTGTCAAGGGTGGTTATAAGTTAT__AATAACTTAAATACTTCACAAAACCTTGGGCT TAA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:554500..554645 32194978 MeRIP-seq:(Medium) rs1564843841 Functional Loss DEL dbSNP153 32..33 33 - - - 95697 RMVar_ID_95697 Human_SNP_ID_418907023 m1A Human chr10 - 587210 587210 587210 CCCCTCGCCACGCTGTCAGCAGGGACCCGGGTAGTCTGGCCTTAGACCCTGCACTGTTTGCCCCT CCCCTCGCCACGCTGTCAGCAGGGACCCGGGTGGTCTGGCCTTAGACCCTGCACTGTTTGCCCCT T C DIP2C Ensembl:ENSG00000151240 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:587207..587359 32194978 MeRIP-seq:(Medium) rs570470559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23462223 95698 RMVar_ID_95698 Human_SNP_ID_418915311 m1A Human chr10 + 607126 607126 607126 CACCCTGCTCACCTCGGTGGGGCTCTCCTGCCAAGGAGGATGGCCCTGAAGTCCGCTGAGATTTC CACCCTGCTCACCTCGGTGGGGCTCTCCTGCCGAGGAGGATGGCCCTGAAGTCCGCTGAGATTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:607120..607292 32194978 MeRIP-seq:(Medium) rs1354256619 Functional Loss SNV dbSNP153 33..33 33 - - - 95699 RMVar_ID_95699 Human_SNP_ID_418922456 m1A Human chr10 + 623595 623595 623595 GGGGAGGGATGCAGGGCTGAGGGGAGGAGGGGAGGGACGCAGGGCCGAGGGCTGAGGGGAGGAGG GGGGAGGGATGCAGGGCTGAGGGGAGGAGGGGGGGGACGCAGGGCCGAGGGCTGAGGGGAGGAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:623591..623805 32194978 MeRIP-seq:(Medium) rs1033317796 Functional Loss SNV dbSNP153 33..33 33 - - - 95700 RMVar_ID_95700 Human_SNP_ID_418937395 m1A Human chr10 + 671435 671435 671435 TCACAGACGCACGGACGGAGGAAACGTCACAGACGCACGGACGGAGGAAACAGACCACAGGCGCA TCACAGACGCACGGACGGAGGAAACGTCACAGGCGCACGGACGGAGGAAACAGACCACAGGCGCA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:671321..671792 26863196 MeRIP-seq:(Medium) rs1295013144 Functional Loss SNV dbSNP153 33..33 33 - - - 95701 RMVar_ID_95701 Human_SNP_ID_418940547 m1A Human chr10 - 679984 679984 679984 GAATGGGGCTAATAAACCGACTGTCAGGATTAATGTGGATCAGATGCGCTCATCTCACAGCCCTG GAATGGGGCTAATAAACCGACTGTCAGGATTACTGTGGATCAGATGCGCTCATCTCACAGCCCTG T G DIP2C Ensembl:ENSG00000151240 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:679982..680174 32194978 MeRIP-seq:(Medium) rs1443940246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9413662,Human_RBP_ID_11410025,Human_RBP_ID_19539705,Human_RBP_ID_22470807,Human_RBP_ID_22694918 95702 RMVar_ID_95702 Human_SNP_ID_418978817 m1A Human chr10 + 812099 812099 812099 GAGTGCTGGGGAACACGGACAGAAATGTGCACAGAGCAGGGCCGGGGCCATCAGCTCACAGGGGT GAGTGCTGGGGAACACGGACAGAAATGTGCACCGAGCAGGGCCGGGGCCATCAGCTCACAGGGGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:812009..812172 26863196 MeRIP-seq:(Medium) rs928011168 Functional Loss SNV dbSNP153 33..33 33 - - - 95703 RMVar_ID_95703 Human_SNP_ID_418992314 m1A Human chr10 - 864200 864200 864200 AGAAGTGTGGGGGGCTCCTGTGTTACATCTGGAAGCAAGCAGTGCTGCTGACGGTGTGAGTGCTG AGAAGTGTGGGGGGCTCCTGTGTTACATCTGGCAGCAAGCAGTGCTGCTGACGGTGTGAGTGCTG T G LARP4B Ensembl:ENSG00000107929 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:864151..864200 26863196 MeRIP-seq:(Medium) rs749552065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747248,Human_RBP_ID_1451323,Human_RBP_ID_3937626,Human_RBP_ID_5545904,Human_RBP_ID_8763951,Human_RBP_ID_9274059,Human_RBP_ID_18969821,Human_RBP_ID_22886791,Human_RBP_ID_23475571 Human_Splice_Rec_1106434,Human_Splice_Rec_1106435,Human_Splice_Rec_1106494,Human_Splice_Rec_1106495,Human_Splice_Rec_1106504,Human_Splice_Rec_1106505,Human_Splice_Rec_1106514,Human_Splice_Rec_1106522 RMVar_hsa_circ_97510,RMVar_hsa_circ_141516,RMVar_hsa_circ_338899,RMVar_hsa_circ_115878,RMVar_hsa_circ_141518,RMVar_hsa_circ_88106,RMVar_hsa_circ_141519,RMVar_hsa_circ_24297,RMVar_hsa_circ_347361,RMVar_hsa_circ_78586,RMVar_hsa_circ_141520,RMVar_hsa_circ_105590,RMVar_hsa_circ_57317,RMVar_hsa_circ_122651,RMVar_hsa_circ_141521,RMVar_hsa_circ_16939,RMVar_hsa_circ_284369,RMVar_hsa_circ_141523,RMVar_hsa_circ_307949,RMVar_hsa_circ_103415,RMVar_hsa_circ_141526,RMVar_hsa_circ_141527,RMVar_hsa_circ_83994,RMVar_hsa_circ_141530,RMVar_hsa_circ_126961,RMVar_hsa_circ_141528,RMVar_hsa_circ_82505,RMVar_hsa_circ_141529,RMVar_hsa_circ_291509,RMVar_hsa_circ_286816,RMVar_hsa_circ_99469,RMVar_hsa_circ_141532,RMVar_hsa_circ_141531,RMVar_hsa_circ_331880,RMVar_hsa_circ_288999,RMVar_hsa_circ_3553,RMVar_hsa_circ_141535,RMVar_hsa_circ_141536,RMVar_hsa_circ_82430,RMVar_hsa_circ_141537,RMVar_hsa_circ_271385,RMVar_hsa_circ_280882,RMVar_hsa_circ_341191,RMVar_hsa_circ_122334,RMVar_hsa_circ_118745,RMVar_hsa_circ_141540,RMVar_hsa_circ_141541,RMVar_hsa_circ_141539,RMVar_hsa_circ_316961,RMVar_hsa_circ_141542 95704 RMVar_ID_95704 Human_SNP_ID_419010223 m1A Human chr10 - 930941 930941 930941 CGGGGCCGGGGTCGCGGGCCGCGAGCGCCCCCAGGCCGGGCGGGCGCCGGCACCCGCAGTGCGGC CGGGGCCGGGGTCGCGGGCCGCGAGCGCCCCCCGGCCGGGCGGGCGCCGGCACCCGCAGTGCGGC T G LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:930909..931269 26863196 MeRIP-seq:(Medium) rs1250107118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748511,Human_RBP_ID_3363311,Human_RBP_ID_5163547,Human_RBP_ID_8172092,Human_RBP_ID_8228796,Human_RBP_ID_9320447,Human_RBP_ID_9413251,Human_RBP_ID_17106987,Human_RBP_ID_18456016,Human_RBP_ID_18475873,Human_RBP_ID_22352169,Human_RBP_ID_23266080,Human_RBP_ID_26767679,Human_RBP_ID_26774830 95705 RMVar_ID_95705 Human_SNP_ID_419010315 m1A Human chr10 + 931152 931150 931152 CCCCTGCCCCGGCCTCGGCCATCCTCAGCCCCAGTTTTCCCCTGCCCCGGCCCCGGTCCTCCTCA CCCCTGCCCCGGCCTCGGCCATCCTCAGCCC__GTTTTCCCCTGCCCCGGCCCCGGTCCTCCTCA CCA C LOC101927762 RNACentral:URS00008B4E7F lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:931030..931213 26863196 MeRIP-seq:(Medium) rs1419842868 Functional Loss DEL dbSNP153 32..33 33 - - - 95706 RMVar_ID_95706 Human_SNP_ID_419010316 m1A Human chr10 + 931152 931152 931152 CCCCTGCCCCGGCCTCGGCCATCCTCAGCCCCAGTTTTCCCCTGCCCCGGCCCCGGTCCTCCTCA CCCCTGCCCCGGCCTCGGCCATCCTCAGCCCCCGTTTTCCCCTGCCCCGGCCCCGGTCCTCCTCA A C LOC101927762 RNACentral:URS00008B4E7F lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:931030..931213 26863196 MeRIP-seq:(Medium) rs1252964027 Functional Loss SNV dbSNP153 33..33 33 - - - 95707 RMVar_ID_95707 Human_SNP_ID_419010533 m1A Human chr10 - 931621 931621 931621 GGGGTTGAGACATTTTCGGGCCCGAAAGGGGAAGAATCCGCCGCCGCCGCCGCCGCCAGCTCGCG GGGGTTGAGACATTTTCGGGCCCGAAAGGGGAGGAATCCGCCGCCGCCGCCGCCGCCAGCTCGCG T C LARP4B Ensembl:ENSG00000107929 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Wild Type chr10:931505..931675;chr10:931526..931675 26863196,26863410 MeRIP-seq:(Medium) rs1309261753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3364515,Human_RBP_ID_4136120,Human_RBP_ID_9320452,Human_RBP_ID_18416062,Human_RBP_ID_18432214,Human_RBP_ID_18475876,Human_RBP_ID_22532216,Human_RBP_ID_26775111 95708 RMVar_ID_95708 Human_SNP_ID_419010779 m1A Human chr10 - 932128 932128 932128 GGGTCTGGGGACAGGCTAGGGCCGGGGTCGCCATCCGTCCTGGGCGGCGGGCAGGGGTCTTTAAG GGGTCTGGGGACAGGCTAGGGCCGGGGTCGCCCTCCGTCCTGGGCGGCGGGCAGGGGTCTTTAAG T G lnc-LARP4B-1 RNACentral:URS00008C33A6 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:932081..932169 26863196 MeRIP-seq:(Medium) rs1373744106 Functional Loss SNV dbSNP153 33..33 33 - - - 95709 RMVar_ID_95709 Human_SNP_ID_419010895 m1A Human chr10 - 932340 932340 932340 TTGGTCCCGGGTGTGGGGTGGGAGTTCGGGGCAGGGCCGGGGCCTGGGTCCCGGGTGTGGGGTGA TTGGTCCCGGGTGTGGGGTGGGAGTTCGGGGCTGGGCCGGGGCCTGGGTCCCGGGTGTGGGGTGA T A lnc-LARP4B-1 RNACentral:URS00008C33A6 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:932290..932434 26863196 MeRIP-seq:(Medium) rs1163250259 Functional Loss SNV dbSNP153 33..33 33 - - - 95710 RMVar_ID_95710 Human_SNP_ID_419025610 m1A Human chr10 + 988212 988212 988212 GCAGTCTGTCGGAAACCCCCGCTTTACTCAGCAGGAATTTAGTCTCCGCGCTCCCCCTAAAACCC GCAGTCTGTCGGAAACCCCCGCTTTACTCAGCCGGAATTTAGTCTCCGCGCTCCCCCTAAAACCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:988163..988255 26863196 MeRIP-seq:(Medium) rs1359689513 Functional Loss SNV dbSNP153 33..33 33 - - - 95711 RMVar_ID_95711 Human_SNP_ID_419025787 m1A Human chr10 + 988526 988526 988526 CTTCAAGAAAATTACGGTGGTGCCGTCCGCCAAGGTAGGCGGCCCCGGGAGGGCCACTGCAACTT CTTCAAGAAAATTACGGTGGTGCCGTCCGCCAGGGTAGGCGGCCCCGGGAGGGCCACTGCAACTT A G GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:988481..988579;chr10:988492..988582 26863196 MeRIP-seq:(Medium) rs201885506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136122,Human_RBP_ID_18416064,Human_RBP_ID_19045127 Human_Splice_Rec_1106529,Human_Splice_Rec_1106559 95712 RMVar_ID_95712 Human_SNP_ID_419025788 m1A Human chr10 + 988526 988526 988526 CTTCAAGAAAATTACGGTGGTGCCGTCCGCCAAGGTAGGCGGCCCCGGGAGGGCCACTGCAACTT CTTCAAGAAAATTACGGTGGTGCCGTCCGCCATGGTAGGCGGCCCCGGGAGGGCCACTGCAACTT A T GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:988481..988579;chr10:988492..988582 26863196 MeRIP-seq:(Medium) rs201885506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136122,Human_RBP_ID_18416064,Human_RBP_ID_19045127 Human_Splice_Rec_1106529,Human_Splice_Rec_1106559 95713 RMVar_ID_95713 Human_SNP_ID_419028037 m1A Human chr10 + 996237 996237 996237 CAAGAGGCAGAAGCAGAGTTTGGAGTATTTGGAGCAAGGTGCTTGTCACGCATCCGCGGGAACCG CAAGAGGCAGAAGCAGAGTTTGGAGTATTTGGGGCAAGGTGCTTGTCACGCATCCGCGGGAACCG A G GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:992634..996277 32194978 MeRIP-seq:(Medium) rs1414831594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861056,Human_RBP_ID_1440681,Human_RBP_ID_5920245,Human_RBP_ID_9360056,Human_RBP_ID_11243980,Human_RBP_ID_23430757 Human_Splice_Rec_1106535,Human_Splice_Rec_1106585 RMVar_hsa_circ_5835,RMVar_hsa_circ_302583,RMVar_hsa_circ_336595,RMVar_hsa_circ_280435,RMVar_hsa_circ_289665,RMVar_hsa_circ_107063,RMVar_hsa_circ_78785,RMVar_hsa_circ_141547,RMVar_hsa_circ_141548,RMVar_hsa_circ_141549,RMVar_hsa_circ_304483,RMVar_hsa_circ_141546,RMVar_hsa_circ_141550,RMVar_hsa_circ_141551,RMVar_hsa_circ_46618 95714 RMVar_ID_95714 Human_SNP_ID_419031040 m1A Human chr10 + 1007110 1007110 1007110 GAGGTGCTGAATAGACTGCACCTGGCTATCCCAACCAGGAGGGACGATAAGGTAAGACGGCCCCT GAGGTGCTGAATAGACTGCACCTGGCTATCCCGACCAGGAGGGACGATAAGGTAAGACGGCCCCT A G GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1007060..1007182 26863196 MeRIP-seq:(Medium) rs1564469322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_981280,Human_RBP_ID_5922040,Human_RBP_ID_8757357,Human_RBP_ID_8981808,Human_RBP_ID_9320792,Human_RBP_ID_11250418,Human_RBP_ID_18586139,Human_RBP_ID_18969825,Human_RBP_ID_22489305,Human_RBP_ID_23431815,Human_RBP_ID_26316017,Human_RBP_ID_27602301 Human_Splice_Rec_1106546,Human_Splice_Rec_1106547,Human_Splice_Rec_1106572,Human_Splice_Rec_1106573,Human_Splice_Rec_1106588 RMVar_hsa_circ_68391,RMVar_hsa_circ_58417,RMVar_hsa_circ_302583,RMVar_hsa_circ_107063,RMVar_hsa_circ_304483,RMVar_hsa_circ_141546,RMVar_hsa_circ_141550,RMVar_hsa_circ_375922,RMVar_hsa_circ_101346,RMVar_hsa_circ_7166,RMVar_hsa_circ_141552,RMVar_hsa_circ_304700,RMVar_hsa_circ_76810,RMVar_hsa_circ_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_337852,RMVar_hsa_circ_301685,RMVar_hsa_circ_141556,RMVar_hsa_circ_141558,RMVar_hsa_circ_141557,RMVar_hsa_circ_311472,RMVar_hsa_circ_64236,RMVar_hsa_circ_286970,RMVar_hsa_circ_70613,RMVar_hsa_circ_141562 95715 RMVar_ID_95715 Human_SNP_ID_419032114 m1A Human chr10 + 1010461 1010461 1010461 ATTTAATGAATTTGTCTGAAAAACATGATAAGATACCAGAAATCTGGGAAGGCCATAATATAGCT ATTTAATGAATTTGTCTGAAAAACATGATAAGGTACCAGAAATCTGGGAAGGCCATAATATAGCT A G GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:1009571..1010511 32194978 MeRIP-seq:(Medium) rs748069913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780,Human_RBP_ID_861783,Human_RBP_ID_1440980,Human_RBP_ID_1759426,Human_RBP_ID_2188119,Human_RBP_ID_9360060,Human_RBP_ID_22876927,Human_RBP_ID_24777813,Human_RBP_ID_26316026 Human_Splice_Rec_1106552,Human_Splice_Rec_1106553,Human_Splice_Rec_1106578 RMVar_hsa_circ_68391,RMVar_hsa_circ_58417,RMVar_hsa_circ_107063,RMVar_hsa_circ_141546,RMVar_hsa_circ_375922,RMVar_hsa_circ_101346,RMVar_hsa_circ_7166,RMVar_hsa_circ_141552,RMVar_hsa_circ_141556,RMVar_hsa_circ_141563,RMVar_hsa_circ_70613,RMVar_hsa_circ_278636,RMVar_hsa_circ_369679,RMVar_hsa_circ_303519 95716 RMVar_ID_95716 Human_SNP_ID_419034224 m1A Human chr10 - 1015863 1015863 1015863 TTGACATCCCTAAGACCAGAAACGTCACGTGGAGTTCGAGAGCAACTCCCACTCCGGGCCACAGA TTGACATCCCTAAGACCAGAAACGTCACGTGGCGTTCGAGAGCAACTCCCACTCCGGGCCACAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:1015812..1017275 32194978 MeRIP-seq:(Medium) rs1234903735 Functional Loss SNV dbSNP153 33..33 33 - - - 95717 RMVar_ID_95717 Human_SNP_ID_419034567 m1A Human chr10 - 1017129 1017129 1017129 CACGTGTCTATCCGCCTCCCCTTTCTTCCCCAACCGATTCATCTTCTTCTGAGCATTCTTCATCA CACGTGTCTATCCGCCTCCCCTTTCTTCCCCATCCGATTCATCTTCTTCTGAGCATTCTTCATCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:1017076..1017225;chr10:1017076..1017230 26863196 MeRIP-seq:(Medium) rs551089723 Functional Loss SNV dbSNP153 33..33 33 - - - 95718 RMVar_ID_95718 Human_SNP_ID_419034717 m1A Human chr10 + 1017640 1017640 1017640 AATTATTTTCTAGTCTTATTTTACAATGTCTCATTGTAGTCTGTCTTCAACTATTTTATCCAAAA AATTATTTTCTAGTCTTATTTTACAATGTCTCGTTGTAGTCTGTCTTCAACTATTTTATCCAAAA A G GTPBP4 Ensembl:ENSG00000107937 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:1017589..1017690 32194978 MeRIP-seq:(Medium) rs1206325308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_369388,Human_RBP_ID_1441062,Human_RBP_ID_1759539,Human_RBP_ID_2188406,Human_RBP_ID_3337588,Human_RBP_ID_4138659,Human_RBP_ID_5922686,Human_RBP_ID_9272264,Human_RBP_ID_11252962,Human_RBP_ID_16979907,Human_RBP_ID_17230418,Human_RBP_ID_17342113,Human_RBP_ID_17457577,Human_RBP_ID_17768778,Human_RBP_ID_18586292,Human_RBP_ID_22787500,Human_RBP_ID_23264247,Human_RBP_ID_24401029,Human_RBP_ID_24458345,Human_RBP_ID_26399542,Human_RBP_ID_26593420,Human_RBP_ID_26874338,Human_RBP_ID_27189764,Human_RBP_ID_27602397 RMVar_hsa_circ_101346,RMVar_hsa_circ_141556 95719 RMVar_ID_95719 Human_SNP_ID_419042816 m1A Human chr10 + 1046540 1046540 1046540 ACACAGCCCAGCTGCTCCACTGTCTACACCACACCGCCCAGCTGCTCCACTGTCTACACCACACA ACACAGCCCAGCTGCTCCACTGTCTACACCACCCCGCCCAGCTGCTCCACTGTCTACACCACACA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1046463..1046582 26863196 MeRIP-seq:(Medium) rs1233628502 Functional Loss SNV dbSNP153 33..33 33 - - - 95720 RMVar_ID_95720 Human_SNP_ID_419042821 m1A Human chr10 - 1046553 1046552 1046553 GGAGCAGCTGGGCTGTGTGGTGTAGACAGTGGAGCAGCTGGGCGGTGTGGTGTAGACAGTGGAGC GGAGCAGCTGGGCTGTGTGGTGTAGACAGTGG_GCAGCTGGGCGGTGTGGTGTAGACAGTGGAGC CT C IDI1 Ensembl:ENSG00000067064 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1046514..1046585 26863196 MeRIP-seq:(Medium) rs76676824 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2106,Human_RBP_ID_805023,Human_RBP_ID_5340308,Human_RBP_ID_5922924,Human_RBP_ID_17106992 RMVar_hsa_circ_126725,RMVar_hsa_circ_141566 95721 RMVar_ID_95721 Human_SNP_ID_419043291 m1A Human chr10 - 1048831 1048829 1048831 GTACTGTGGACGGGCGGCGGAGTTCGGGAGACAGGGGCAGGGCGGCATCGGGGAGCTGCGGGACG GTACTGTGGACGGGCGGCGGAGTTCGGGAGAC__GGGCAGGGCGGCATCGGGGAGCTGCGGGACG CCT C IDI1 Ensembl:ENSG00000067064 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1048671..1049021 26863196 MeRIP-seq:(Medium) rs770886898 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_804791,Human_RBP_ID_5339075,Human_RBP_ID_8172859,Human_RBP_ID_9343334,Human_RBP_ID_9413048,Human_RBP_ID_19045135,Human_RBP_ID_22708185 RMVar_hsa_circ_126725,RMVar_hsa_circ_141566 95722 RMVar_ID_95722 Human_SNP_ID_419043293 m1A Human chr10 - 1048831 1048830 1048831 GTACTGTGGACGGGCGGCGGAGTTCGGGAGACAGGGGCAGGGCGGCATCGGGGAGCTGCGGGACG GTACTGTGGACGGGCGGCGGAGTTCGGGAGAC_GGGGCAGGGCGGCATCGGGGAGCTGCGGGACG CT C IDI1 Ensembl:ENSG00000067064 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1048671..1049021 26863196 MeRIP-seq:(Medium) rs776484724 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_804791,Human_RBP_ID_5339075,Human_RBP_ID_8172859,Human_RBP_ID_9343334,Human_RBP_ID_9413048,Human_RBP_ID_19045135,Human_RBP_ID_22708185 RMVar_hsa_circ_126725,RMVar_hsa_circ_141566 95723 RMVar_ID_95723 Human_SNP_ID_419043294 m1A Human chr10 - 1048831 1048831 1048831 GTACTGTGGACGGGCGGCGGAGTTCGGGAGACAGGGGCAGGGCGGCATCGGGGAGCTGCGGGACG GTACTGTGGACGGGCGGCGGAGTTCGGGAGACTGGGGCAGGGCGGCATCGGGGAGCTGCGGGACG T A IDI1 Ensembl:ENSG00000067064 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1048671..1049021 26863196 MeRIP-seq:(Medium) rs1384918184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804791,Human_RBP_ID_5339075,Human_RBP_ID_8172859,Human_RBP_ID_9343334,Human_RBP_ID_9413048,Human_RBP_ID_19045135,Human_RBP_ID_22708185 RMVar_hsa_circ_126725,RMVar_hsa_circ_141566 95724 RMVar_ID_95724 Human_SNP_ID_419043547 m1A Human chr10 + 1049198 1049198 1049198 CACCCCCAGTTCCGCAGAGGCAGCGTCCCGCGACTGGGCGGTGCCCGAGACCACAGACGCCGCCA CACCCCCAGTTCCGCAGAGGCAGCGTCCCGCGTCTGGGCGGTGCCCGAGACCACAGACGCCGCCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1049151..1049316 26863196 MeRIP-seq:(Medium) rs1028317171 Functional Loss SNV dbSNP153 33..33 33 - - - 95725 RMVar_ID_95725 Human_SNP_ID_419045552 m1A Human chr10 + 1056477 1056476 1056477 CGCGGCCCTGAGCGCAGGCGGCCCCGGGTCTCAGGCCTCAGGCGGACCGCGCCCCGGGCTCGCAG CGCGGCCCTGAGCGCAGGCGGCCCCGGGTCTC_GGCCTCAGGCGGACCGCGCCCCGGGCTCGCAG CA C WDR37 Ensembl:ENSG00000047056 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1056428..1056525 26863196 MeRIP-seq:(Medium) rs1329502224 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18431228 Human_Splice_Rec_1106715,Human_Splice_Rec_1106731 RMVar_hsa_circ_96719,RMVar_hsa_circ_141567,RMVar_hsa_circ_141568 95726 RMVar_ID_95726 Human_SNP_ID_419045751 m1A Human chr10 - 1056881 1056881 1056881 AGTGAGTCCCTACGACGCGGCCCCCCGTACTGACCCGAAGACGCGCAGGACACCGCTGTCTCCGC AGTGAGTCCCTACGACGCGGCCCCCCGTACTGTCCCGAAGACGCGCAGGACACCGCTGTCTCCGC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1056839..1057316 26863196 MeRIP-seq:(Medium) rs952769484 Functional Loss SNV dbSNP153 33..33 33 - - - 95727 RMVar_ID_95727 Human_SNP_ID_419054549 m1A Human chr10 + 1089617 1089617 1089617 AATTCAGCCTTCCCGTGCTCACCCACAATTCAACCTTCCCATGCTCACCCACAATTCAGCCTTCC AATTCAGCCTTCCCGTGCTCACCCACAATTCAGCCTTCCCATGCTCACCCACAATTCAGCCTTCC A G WDR37 Ensembl:ENSG00000047056 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1089567..1089673 26863196 MeRIP-seq:(Medium) rs188097723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32847,RMVar_hsa_circ_102551,RMVar_hsa_circ_141569,RMVar_hsa_circ_279940,RMVar_hsa_circ_358576,RMVar_hsa_circ_271460,RMVar_hsa_circ_77793,RMVar_hsa_circ_141576,RMVar_hsa_circ_141577,RMVar_hsa_circ_141575,RMVar_hsa_circ_292794,RMVar_hsa_circ_308563,RMVar_hsa_circ_280793,RMVar_hsa_circ_141579,RMVar_hsa_circ_299703,RMVar_hsa_circ_372153,RMVar_hsa_circ_141578,RMVar_hsa_circ_332653,RMVar_hsa_circ_99762,RMVar_hsa_circ_269819,RMVar_hsa_circ_93767,RMVar_hsa_circ_108265,RMVar_hsa_circ_141584,RMVar_hsa_circ_141586,RMVar_hsa_circ_141587,RMVar_hsa_circ_141588,RMVar_hsa_circ_141585,RMVar_hsa_circ_374895,RMVar_hsa_circ_141590,RMVar_hsa_circ_27193,RMVar_hsa_circ_317805,RMVar_hsa_circ_141589,RMVar_hsa_circ_354106,RMVar_hsa_circ_283756,RMVar_hsa_circ_106737,RMVar_hsa_circ_271314,RMVar_hsa_circ_103960,RMVar_hsa_circ_126370,RMVar_hsa_circ_141591,RMVar_hsa_circ_141593,RMVar_hsa_circ_141595,RMVar_hsa_circ_141594,RMVar_hsa_circ_141592,RMVar_hsa_circ_141598,RMVar_hsa_circ_98029,RMVar_hsa_circ_141599 95728 RMVar_ID_95728 Human_SNP_ID_419056046 m1A Human chr10 + 1094694 1094694 1094694 CAAACCAAAGGGCTGGAAAAGAGGGTGGAACCAGACACATCCAGGAACTGATGAAGACTTGGAAA CAAACCAAAGGGCTGGAAAAGAGGGTGGAACCGGACACATCCAGGAACTGATGAAGACTTGGAAA A G WDR37 Ensembl:ENSG00000047056 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1094608..1095245 26863196 MeRIP-seq:(Medium) rs936162510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279940,RMVar_hsa_circ_358576,RMVar_hsa_circ_271460,RMVar_hsa_circ_77793,RMVar_hsa_circ_141576,RMVar_hsa_circ_141577,RMVar_hsa_circ_141575,RMVar_hsa_circ_292794,RMVar_hsa_circ_308563,RMVar_hsa_circ_280793,RMVar_hsa_circ_141579,RMVar_hsa_circ_299703,RMVar_hsa_circ_372153,RMVar_hsa_circ_141578,RMVar_hsa_circ_332653,RMVar_hsa_circ_99762,RMVar_hsa_circ_269819,RMVar_hsa_circ_93767,RMVar_hsa_circ_108265,RMVar_hsa_circ_141584,RMVar_hsa_circ_141586,RMVar_hsa_circ_141587,RMVar_hsa_circ_141588,RMVar_hsa_circ_141585,RMVar_hsa_circ_374895,RMVar_hsa_circ_141590,RMVar_hsa_circ_27193,RMVar_hsa_circ_317805,RMVar_hsa_circ_141589,RMVar_hsa_circ_354106,RMVar_hsa_circ_283756,RMVar_hsa_circ_106737,RMVar_hsa_circ_271314,RMVar_hsa_circ_103960,RMVar_hsa_circ_51951,RMVar_hsa_circ_126370,RMVar_hsa_circ_141591,RMVar_hsa_circ_141593,RMVar_hsa_circ_141595,RMVar_hsa_circ_141594,RMVar_hsa_circ_141592,RMVar_hsa_circ_141599,RMVar_hsa_circ_294748,RMVar_hsa_circ_288881,RMVar_hsa_circ_141600,RMVar_hsa_circ_141601 95729 RMVar_ID_95729 Human_SNP_ID_419056149 m1A Human chr10 + 1095060 1095060 1095060 GTAATGGGTATAGAGAGGAGAGTTAGACTGGGAAACGTGAGGTAATGGGCATGGAGAGAGGAGGG GTAATGGGTATAGAGAGGAGAGTTAGACTGGGCAACGTGAGGTAATGGGCATGGAGAGAGGAGGG A C WDR37 Ensembl:ENSG00000047056 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1095012..1095096 26863196 MeRIP-seq:(Medium) rs1480045851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_370118,Human_RBP_ID_23434206 RMVar_hsa_circ_279940,RMVar_hsa_circ_358576,RMVar_hsa_circ_271460,RMVar_hsa_circ_77793,RMVar_hsa_circ_141576,RMVar_hsa_circ_141577,RMVar_hsa_circ_141575,RMVar_hsa_circ_292794,RMVar_hsa_circ_308563,RMVar_hsa_circ_280793,RMVar_hsa_circ_141579,RMVar_hsa_circ_299703,RMVar_hsa_circ_372153,RMVar_hsa_circ_141578,RMVar_hsa_circ_332653,RMVar_hsa_circ_99762,RMVar_hsa_circ_269819,RMVar_hsa_circ_93767,RMVar_hsa_circ_108265,RMVar_hsa_circ_141584,RMVar_hsa_circ_141586,RMVar_hsa_circ_141587,RMVar_hsa_circ_141588,RMVar_hsa_circ_141585,RMVar_hsa_circ_374895,RMVar_hsa_circ_141590,RMVar_hsa_circ_27193,RMVar_hsa_circ_317805,RMVar_hsa_circ_141589,RMVar_hsa_circ_354106,RMVar_hsa_circ_283756,RMVar_hsa_circ_106737,RMVar_hsa_circ_271314,RMVar_hsa_circ_103960,RMVar_hsa_circ_51951,RMVar_hsa_circ_126370,RMVar_hsa_circ_141591,RMVar_hsa_circ_141593,RMVar_hsa_circ_141595,RMVar_hsa_circ_141594,RMVar_hsa_circ_141592,RMVar_hsa_circ_141599,RMVar_hsa_circ_294748,RMVar_hsa_circ_288881,RMVar_hsa_circ_141600,RMVar_hsa_circ_141601 95730 RMVar_ID_95730 Human_SNP_ID_419056206 m1A Human chr10 - 1095228 1095226 1095229 CCCCTCTCCATGCCCATTACCTCACGTTTCCAAGTCTAACTCTCCTCTCTCCATGCTCGTCACCT CCCCTCTCCATGCCCATTACCTCACGTTTCC___TCTAACTCTCCTCTCTCCATGCTCGTCACCT ACTT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1095177..1095441 26863196 MeRIP-seq:(Medium) rs1357626198 Functional Loss DEL dbSNP153 32..34 33 - - - 95731 RMVar_ID_95731 Human_SNP_ID_419056273 m1A Human chr10 - 1095444 1095444 1095444 TGCAACTCCTCCTCAAATCAACATCATGCCCAATCCCAGTCTAACTCTCCTCTCTCCATGCCCGT TGCAACTCCTCCTCAAATCAACATCATGCCCAGTCCCAGTCTAACTCTCCTCTCTCCATGCCCGT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1095296..1095525 26863196 MeRIP-seq:(Medium) rs1008032736 Functional Loss SNV dbSNP153 33..33 33 - - - 95732 RMVar_ID_95732 Human_SNP_ID_419082043 m1A Human chr10 - 1187348 1187348 1187348 AGGAGGGGAGGCCGCCTGGTGACGGGAGTGGGAGGAGGAGGGGAGGCTGCCCAGTGCACGCAGAT AGGAGGGGAGGCCGCCTGGTGACGGGAGTGGGGGGAGGAGGGGAGGCTGCCCAGTGCACGCAGAT T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1187342..1187425 26863196 MeRIP-seq:(Medium) rs925114013 Functional Loss SNV dbSNP153 33..33 33 - - - 95733 RMVar_ID_95733 Human_SNP_ID_419088230 m1A Human chr10 + 1209513 1209495 1209513 ATGCCTACACTGTCGCCCATGCCTACACTGTCACCCATGCCCACACCTACAGCCTCGCCCACACC ATGCCTACACTGTCG__________________CCCATGCCCACACCTACAGCCTCGCCCACACC GCCCATGCCTACACTGTCA G LINC00200 Ensembl:ENSG00000229205 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1209209..1209790;chr10:1209204..1209776 26863196 MeRIP-seq:(Medium) rs1179310662 Functional Loss DEL dbSNP153 16..33 33 - - - 95734 RMVar_ID_95734 Human_SNP_ID_419088249 m1A Human chr10 + 1209513 1209513 1209513 ATGCCTACACTGTCGCCCATGCCTACACTGTCACCCATGCCCACACCTACAGCCTCGCCCACACC ATGCCTACACTGTCGCCCATGCCTACACTGTCGCCCATGCCCACACCTACAGCCTCGCCCACACC A G LINC00200 Ensembl:ENSG00000229205 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1209209..1209790;chr10:1209204..1209776 26863196 MeRIP-seq:(Medium) rs796606906 Functional Loss SNV dbSNP153 33..33 33 - - - 95735 RMVar_ID_95735 Human_SNP_ID_419088250 m1A Human chr10 + 1209513 1209513 1209513 ATGCCTACACTGTCGCCCATGCCTACACTGTCACCCATGCCCACACCTACAGCCTCGCCCACACC ATGCCTACACTGTCGCCCATGCCTACACTGTCTCCCATGCCCACACCTACAGCCTCGCCCACACC A T LINC00200 Ensembl:ENSG00000229205 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1209209..1209790;chr10:1209204..1209776 26863196 MeRIP-seq:(Medium) rs796606906 Functional Loss SNV dbSNP153 33..33 33 - - - 95736 RMVar_ID_95736 Human_SNP_ID_419088259 m1A Human chr10 - 1209528 1209528 1209528 GTGGGTGATGGCATGGGTGTGGGCGAGGCTGTAGGTGTGGGCATGGGTGACAGTGTAGGCATGGG GTGGGTGATGGCATGGGTGTGGGCGAGGCTGTGGGTGTGGGCATGGGTGACAGTGTAGGCATGGG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1209261..1209717 26863196 MeRIP-seq:(Medium) rs1428960138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21433 95737 RMVar_ID_95737 Human_SNP_ID_419088260 m1A Human chr10 - 1209528 1209528 1209528 GTGGGTGATGGCATGGGTGTGGGCGAGGCTGTAGGTGTGGGCATGGGTGACAGTGTAGGCATGGG GTGGGTGATGGCATGGGTGTGGGCGAGGCTGTCGGTGTGGGCATGGGTGACAGTGTAGGCATGGG T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1209261..1209717 26863196 MeRIP-seq:(Medium) rs1428960138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21433 95738 RMVar_ID_95738 Human_SNP_ID_419089203 m1A Human chr10 - 1212739 1212739 1212739 GGCCACTTGGCTGCAGGGTGCCTGCCACGGTGAGGTGGACTCAGGGCCACTTGGCTGCAGGGTGC GGCCACTTGGCTGCAGGGTGCCTGCCACGGTGGGGTGGACTCAGGGCCACTTGGCTGCAGGGTGC T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1212690..1212810 26863196 MeRIP-seq:(Medium) rs1229119552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21433 95739 RMVar_ID_95739 Human_SNP_ID_419098322 m1A Human chr10 - 1239355 1239354 1239355 AGGGGGGAGTAAACACCGGGAGGGAGAGGGGGAGTAAACACCGGGAGGCAGAGGGGAGTAAACAC AGGGGGGAGTAAACACCGGGAGGGAGAGGGGG_GTAAACACCGGGAGGCAGAGGGGAGTAAACAC CT C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1239296..1239403 26863196 MeRIP-seq:(Medium) rs1424804488 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_16190,RMVar_hsa_circ_21433,RMVar_hsa_circ_312016 95740 RMVar_ID_95740 Human_SNP_ID_419103039 m1A Human chr10 - 1253936 1253936 1253936 CACAGAACCCACCGTATCCTAACCCAGAGCCCATCGCATCTTAACCAGATCCCACATTTTACCCA CACAGAACCCACCGTATCCTAACCCAGAGCCCGTCGCATCTTAACCAGATCCCACATTTTACCCA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1253933..1254137 26863196 MeRIP-seq:(Medium) rs1490361962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16190,RMVar_hsa_circ_21433,RMVar_hsa_circ_312016 95741 RMVar_ID_95741 Human_SNP_ID_419116823 m1A Human chr10 + 1300375 1300375 1300375 ACGGCTGCTCCCAGCCTCTCACACCACACCACACAGCCAGGCTGATGCCAGCTCCACGCCCCCCA ACGGCTGCTCCCAGCCTCTCACACCACACCACGCAGCCAGGCTGATGCCAGCTCCACGCCCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1300373..1300496 26863196 MeRIP-seq:(Medium) rs191231349 Functional Loss SNV dbSNP153 33..33 33 - - - 95742 RMVar_ID_95742 Human_SNP_ID_419124373 m1A Human chr10 + 1327382 1327382 1327382 CCTCCTCACGGCCCAGCGCCTCCCCACGGCACAGCGCCTCCCCACTGCACAGCGCCTCCCCACTG CCTCCTCACGGCCCAGCGCCTCCCCACGGCACGGCGCCTCCCCACTGCACAGCGCCTCCCCACTG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:1327372..1327532 26863196 MeRIP-seq:(Medium) rs1347370658 Functional Loss SNV dbSNP153 33..33 33 - - - 95743 RMVar_ID_95743 Human_SNP_ID_419124392 m1A Human chr10 - 1327413 1327413 1327413 GGGAGGCGCTGGGCAGTGGGGAGGCGCTGGGCAGTGGGGAGGCGCTGTGCAGTGGGGAGGCGCTG GGGAGGCGCTGGGCAGTGGGGAGGCGCTGGGCTGTGGGGAGGCGCTGTGCAGTGGGGAGGCGCTG T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1327399..1327537 26863196 MeRIP-seq:(Medium) rs865854374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24430 95744 RMVar_ID_95744 Human_SNP_ID_419124393 m1A Human chr10 - 1327413 1327413 1327413 GGGAGGCGCTGGGCAGTGGGGAGGCGCTGGGCAGTGGGGAGGCGCTGTGCAGTGGGGAGGCGCTG GGGAGGCGCTGGGCAGTGGGGAGGCGCTGGGCCGTGGGGAGGCGCTGTGCAGTGGGGAGGCGCTG T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1327399..1327537 26863196 MeRIP-seq:(Medium) rs865854374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24430 95745 RMVar_ID_95745 Human_SNP_ID_419124472 m1A Human chr10 + 1327524 1327506 1327524 CGCCTCCTCACTGCCCAGCGCCTCCCCATGGCACAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC CGCCTCCTCACTGCC__________________CAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC CCAGCGCCTCCCCATGGCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1327067..1327952;chr10:1327054..1327991 26863196 MeRIP-seq:(Medium) rs1564258453 Functional Loss DEL dbSNP153 16..33 33 - - - 95746 RMVar_ID_95746 Human_SNP_ID_419124486 m1A Human chr10 + 1327524 1327524 1327524 CGCCTCCTCACTGCCCAGCGCCTCCCCATGGCACAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC CGCCTCCTCACTGCCCAGCGCCTCCCCATGGCCCAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1327067..1327952;chr10:1327054..1327991 26863196 MeRIP-seq:(Medium) rs1257869701 Functional Loss SNV dbSNP153 33..33 33 - - - 95747 RMVar_ID_95747 Human_SNP_ID_419124487 m1A Human chr10 + 1327524 1327524 1327524 CGCCTCCTCACTGCCCAGCGCCTCCCCATGGCACAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC CGCCTCCTCACTGCCCAGCGCCTCCCCATGGCTCAGCGCCTCCTCACTGCCCAGCGCCTCCTCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1327067..1327952;chr10:1327054..1327991 26863196 MeRIP-seq:(Medium) rs1257869701 Functional Loss SNV dbSNP153 33..33 33 - - - 95748 RMVar_ID_95748 Human_SNP_ID_419130636 m1A Human chr10 - 1349139 1349139 1349139 CATAAGGTAATGTCATCATCAGTTAAGGCAGGAACAGGCCATTTTCACTTCTTTTGTGGTGGAAT CATAAGGTAATGTCATCATCAGTTAAGGCAGGTACAGGCCATTTTCACTTCTTTTGTGGTGGAAT T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1349133..1349297 26863196 MeRIP-seq:(Medium) rs1365766083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24430 95749 RMVar_ID_95749 Human_SNP_ID_419143859 m1A Human chr10 - 1396817 1396817 1396817 ACCCAGGAAGCCTCCACTCGGGAGGGGAGAGGAGGACGGTGACCCAGGAAGCCTCCACTCGGGAG ACCCAGGAAGCCTCCACTCGGGAGGGGAGAGGCGGACGGTGACCCAGGAAGCCTCCACTCGGGAG T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1396815..1396980 26863196 MeRIP-seq:(Medium) rs4880505 Functional Loss SNV dbSNP153 33..33 33 - - - 95750 RMVar_ID_95750 Human_SNP_ID_419156745 m1A Human chr10 + 1444319 1444319 1444319 ATCCATCCATCCATCCATCCATCCACTCATTCATCCTTCCATCCACCCAGCCATCCACTCACCCA ATCCATCCATCCATCCATCCATCCACTCATTCGTCCTTCCATCCACCCAGCCATCCACTCACCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1444317..1445574 26863196 MeRIP-seq:(Medium) rs1243306560 Functional Loss SNV dbSNP153 33..33 33 - - - 95751 RMVar_ID_95751 Human_SNP_ID_419156751 m1A Human chr10 + 1444327 1444327 1444327 ATCCATCCATCCATCCACTCATTCATCCTTCCATCCACCCAGCCATCCACTCACCCATCCACTCA ATCCATCCATCCATCCACTCATTCATCCTTCCCTCCACCCAGCCATCCACTCACCCATCCACTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1444324..1445585 26863196 MeRIP-seq:(Medium) rs1264892922 Functional Loss SNV dbSNP153 33..33 33 - - - 95752 RMVar_ID_95752 Human_SNP_ID_419156790 m1A Human chr10 + 1444436 1444433 1444437 CATCTATCCATCCTCTATCCATCCACCCACCCATCCATCCATTGATCATCCATCTATCTACATTC CATCTATCCATCCTCTATCCATCCACCCAC____CCATCCATTGATCATCCATCTATCTACATTC CCCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1444429..1444671 26863196 MeRIP-seq:(Medium) rs1482971264 Functional Loss DEL dbSNP153 31..34 33 - - - 95753 RMVar_ID_95753 Human_SNP_ID_419156978 m1A Human chr10 - 1445031 1445031 1445031 TTAATGTAGATGGATGGATGGTGAATGAGTGAATGGATGGGTGAGTGGATGGACGGATGAATGTA TTAATGTAGATGGATGGATGGTGAATGAGTGACTGGATGGGTGAGTGGATGGACGGATGAATGTA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1444872..1445069 26863196 MeRIP-seq:(Medium) rs1174061448 Functional Loss SNV dbSNP153 33..33 33 - - - 95754 RMVar_ID_95754 Human_SNP_ID_419165758 m1A Human chr10 - 1474816 1474816 1474816 CGCCTCCTCCCGGAGTCCTGCTCAGCACTCTTACACAGGCGTTTCCATCCCGACTTTGCACACGT CGCCTCCTCCCGGAGTCCTGCTCAGCACTCTTCCACAGGCGTTTCCATCCCGACTTTGCACACGT T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:1474769..1474956 26863196 MeRIP-seq:(Medium) rs1032289797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2202074 95755 RMVar_ID_95755 Human_SNP_ID_419166531 m1A Human chr10 + 1477404 1477404 1477404 CAGCATGACCTTATCTGCCCATGGCCCCCTCCAGCATGACCCTATACAGCTTCCTTCCAGCCCTG CAGCATGACCTTATCTGCCCATGGCCCCCTCCGGCATGACCCTATACAGCTTCCTTCCAGCCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1477401..1477532 26863196 MeRIP-seq:(Medium) rs1419697201 Functional Loss SNV dbSNP153 33..33 33 - - - 95756 RMVar_ID_95756 Human_SNP_ID_419171673 m1A Human chr10 + 1495794 1495794 1495794 TCATTGTTATCATCATCATCATTGGTATAAACATCATCACCATCATCATCACTGTCATCATCACC TCATTGTTATCATCATCATCATTGGTATAAACTTCATCACCATCATCATCACTGTCATCATCACC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1495792..1496001 26863196 MeRIP-seq:(Medium) rs1356412394 Functional Loss SNV dbSNP153 33..33 33 - - - 95757 RMVar_ID_95757 Human_SNP_ID_419171847 m1A Human chr10 - 1496269 1496269 1496269 TGATGGTGACTATGATGATGATAAAGTTGATGATGATGGTGCTGATGACAATGATGATGGTGATA TGATGGTGACTATGATGATGATAAAGTTGATGCTGATGGTGCTGATGACAATGATGATGGTGATA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1496267..1496447 26863196 MeRIP-seq:(Medium) rs903320930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141622 95758 RMVar_ID_95758 Human_SNP_ID_419172719 m1A Human chr10 + 1499456 1499456 1499456 TCTATTACTTATTACTCACTAATCGCTCACTCATTACTCACTCATCATTCAGTTGTCAGCTACTC TCTATTACTTATTACTCACTAATCGCTCACTCTTTACTCACTCATCATTCAGTTGTCAGCTACTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1499448..1499690 26863196 MeRIP-seq:(Medium) rs941000909 Functional Loss SNV dbSNP153 33..33 33 - - - 95759 RMVar_ID_95759 Human_SNP_ID_419172743 m1A Human chr10 - 1499541 1499541 1499541 ATGAGTGAGTGATGAGTGATGAGTGAGACATGAGCGAGTGATGAATAAGTTTGAGTGAGTAATGA ATGAGTGAGTGATGAGTGATGAGTGAGACATGTGCGAGTGATGAATAAGTTTGAGTGAGTAATGA T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1498808..1499917 26863196 MeRIP-seq:(Medium) rs189545767 Functional Loss SNV dbSNP153 33..33 33 - - - 95760 RMVar_ID_95760 Human_SNP_ID_419172753 m1A Human chr10 + 1499575 1499558 1499576 ATGTCTCACTCATCACTCATCACTCACTCATCATTCATCACCCACCACTCATTTTTACTCAACAC ATGTCTCACTCATCAC__________________TCATCACCCACCACTCATTTTTACTCAACAC CTCATCACTCACTCATCAT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1499537..1499671 26863196 MeRIP-seq:(Medium) rs898465124 Functional Loss DEL dbSNP153 17..34 33 - - - 95761 RMVar_ID_95761 Human_SNP_ID_419172758 m1A Human chr10 + 1499575 1499572 1499576 ATGTCTCACTCATCACTCATCACTCACTCATCATTCATCACCCACCACTCATTTTTACTCAACAC ATGTCTCACTCATCACTCATCACTCACTCA____TCATCACCCACCACTCATTTTTACTCAACAC ATCAT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1499537..1499671 26863196 MeRIP-seq:(Medium) rs549112559 Functional Loss DEL dbSNP153 31..34 33 - - - 95762 RMVar_ID_95762 Human_SNP_ID_419175713 m1A Human chr10 - 1510021 1510016 1510021 GAGAAGAGAGAGAAAAGAAAGAAAGAGAAAAAAGAAAGAAGAAAGAAAAGAAAGAAAGAGAAAAA GAGAAGAGAGAGAAAAGAAAGAAAGAGAAAAA_____GAAGAAAGAAAAGAAAGAAAGAGAAAAA CTTTCT C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1510016..1510123 26863196 MeRIP-seq:(Medium) rs1460705407 Functional Loss DEL dbSNP153 33..37 33 - - - 95763 RMVar_ID_95763 Human_SNP_ID_419175715 m1A Human chr10 - 1510021 1510020 1510021 GAGAAGAGAGAGAAAAGAAAGAAAGAGAAAAAAGAAAGAAGAAAGAAAAGAAAGAAAGAGAAAAA GAGAAGAGAGAGAAAAGAAAGAAAGAGAAAAA_GAAAGAAGAAAGAAAAGAAAGAAAGAGAAAAA CT C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1510016..1510123 26863196 MeRIP-seq:(Medium) rs1354470902 Functional Loss DEL dbSNP153 33..33 33 - - - 95764 RMVar_ID_95764 Human_SNP_ID_419181420 m1A Human chr10 + 1529125 1529125 1529125 ATCCTCCAATCAGTCCACGCACCATCCCCAACACAAATCCTCCAATCAGTCCACGCACCATCCCC ATCCTCCAATCAGTCCACGCACCATCCCCAACCCAAATCCTCCAATCAGTCCACGCACCATCCCC A C ADARB2-AS1 Ensembl:ENSG00000205696 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1529117..1529188 26863196 MeRIP-seq:(Medium) rs1220574297 Functional Loss SNV dbSNP153 33..33 33 - - - 95765 RMVar_ID_95765 Human_SNP_ID_419181479 m1A Human chr10 + 1529280 1529280 1529280 AGTCCACGCACCATGCCCAACACCAATCCTCCAATCAGTCCATGCACCATCCCCAACACAAATCC AGTCCACGCACCATGCCCAACACCAATCCTCCCATCAGTCCATGCACCATCCCCAACACAAATCC A C ADARB2-AS1 Ensembl:ENSG00000205696 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1529253..1529352 26863196 MeRIP-seq:(Medium) rs1191513102 Functional Loss SNV dbSNP153 33..33 33 - - - 95766 RMVar_ID_95766 Human_SNP_ID_419181754 m1A Human chr10 - 1530033 1530033 1530033 GCAGTGGATAGGCGCCCATGGTGGCATGAGGTAGTGGACAGGTGCCCACATTGACAGGGACAGTT GCAGTGGATAGGCGCCCATGGTGGCATGAGGTCGTGGACAGGTGCCCACATTGACAGGGACAGTT T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1530026..1530121 26863196 MeRIP-seq:(Medium) rs1428143458 Functional Loss SNV dbSNP153 33..33 33 - - - 95767 RMVar_ID_95767 Human_SNP_ID_419181757 m1A Human chr10 + 1530039 1530039 1530039 CCCTGTCAATGTGGGCACCTGTCCACTACCTCATGCCACCATGGGCGCCTATCCACTGCTTCTGC CCCTGTCAATGTGGGCACCTGTCCACTACCTCCTGCCACCATGGGCGCCTATCCACTGCTTCTGC A C ADARB2-AS1 Ensembl:ENSG00000205696 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1529846..1530227 26863196 MeRIP-seq:(Medium) rs1298289000 Functional Loss SNV dbSNP153 33..33 33 - - - 95768 RMVar_ID_95768 Human_SNP_ID_419184876 m1A Human chr10 - 1540681 1540681 1540681 CAGAGTCCGAACTGCGTCTGAGTGGGGTCTGGACGGCTGTGATCCAGGGTCCAAACTGCGTCTGA CAGAGTCCGAACTGCGTCTGAGTGGGGTCTGGGCGGCTGTGATCCAGGGTCCAAACTGCGTCTGA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1540679..1540752 26863196 MeRIP-seq:(Medium) rs80190010 Functional Loss SNV dbSNP153 33..33 33 - - - 95769 RMVar_ID_95769 Human_SNP_ID_419185284 m1A Human chr10 + 1541952 1541952 1541952 ACAGCCGTCCAGACCCCACTCAGACGCAGTTCAGACCCTGGATCACAGCCGTCCAGACTCCACTC ACAGCCGTCCAGACCCCACTCAGACGCAGTTCGGACCCTGGATCACAGCCGTCCAGACTCCACTC A G ADARB2-AS1 Ensembl:ENSG00000205696 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1541942..1542048 26863196 MeRIP-seq:(Medium) rs1485852518 Functional Loss SNV dbSNP153 33..33 33 - - - 95770 RMVar_ID_95770 Human_SNP_ID_419189747 m1A Human chr10 + 1557111 1557111 1557111 GTCCGAGGGTACCTCTTTCCTTCCATTGCCTCAGTTTCAGGTGTCCAGTCCATGGCGCCCCCCGT GTCCGAGGGTACCTCTTTCCTTCCATTGCCTCCGTTTCAGGTGTCCAGTCCATGGCGCCCCCCGT A C ADARB2-AS1,ADARB2-AS1:2 RNACentral:URS00008B2AFE,RNACentral:URS00008B2318 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1557109..1557262 26863196 MeRIP-seq:(Medium) rs1197060925 Functional Loss SNV dbSNP153 33..33 33 - - - 95771 RMVar_ID_95771 Human_SNP_ID_419189748 m1A Human chr10 + 1557111 1557111 1557111 GTCCGAGGGTACCTCTTTCCTTCCATTGCCTCAGTTTCAGGTGTCCAGTCCATGGCGCCCCCCGT GTCCGAGGGTACCTCTTTCCTTCCATTGCCTCGGTTTCAGGTGTCCAGTCCATGGCGCCCCCCGT A G ADARB2-AS1,ADARB2-AS1:2 RNACentral:URS00008B2AFE,RNACentral:URS00008B2318 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1557109..1557262 26863196 MeRIP-seq:(Medium) rs1197060925 Functional Loss SNV dbSNP153 33..33 33 - - - 95772 RMVar_ID_95772 Human_SNP_ID_419190265 m1A Human chr10 + 1558548 1558548 1558548 CCTCTGTCCCCTTCTGTGGGTGCTCAGCCCCCACGCACCCCATCTAAATCTGCATCCCACCTCTG CCTCTGTCCCCTTCTGTGGGTGCTCAGCCCCCCCGCACCCCATCTAAATCTGCATCCCACCTCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1558546..1558644 26863196 MeRIP-seq:(Medium) rs1267300733 Functional Loss SNV dbSNP153 33..33 33 - - - 95773 RMVar_ID_95773 Human_SNP_ID_419190276 m1A Human chr10 - 1558581 1558581 1558581 AGCATGCAGGGGCTGAGCACCCACAGAAGGGGACAGAGGTGGGATGCAGATTTAGATGGGGTGCG AGCATGCAGGGGCTGAGCACCCACAGAAGGGGGCAGAGGTGGGATGCAGATTTAGATGGGGTGCG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1558544..1558699 26863196 MeRIP-seq:(Medium) rs56191235 Functional Loss SNV dbSNP153 33..33 33 - - - 95774 RMVar_ID_95774 Human_SNP_ID_419190367 m1A Human chr10 - 1558704 1558704 1558704 GATGGAGCATGCGGGGGCTGAGCACCCACAGAAGGGGGCAGAGGTGGGATGTGGATTTAGATGGG GATGGAGCATGCGGGGGCTGAGCACCCACAGAGGGGGGCAGAGGTGGGATGTGGATTTAGATGGG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1558697..1558819 26863196 MeRIP-seq:(Medium) rs113154789 Functional Loss SNV dbSNP153 33..33 33 - - - 95775 RMVar_ID_95775 Human_SNP_ID_419195872 m1A Human chr10 + 1576275 1576275 1576275 GTGGCTTAGGGTCACTGTAGGGCTCAGGGTCAAAGGAGGGGGCTCAGGATCACTGGAGGGGCTCA GTGGCTTAGGGTCACTGTAGGGCTCAGGGTCACAGGAGGGGGCTCAGGATCACTGGAGGGGCTCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1576226..1576408 26863196 MeRIP-seq:(Medium) rs1476960475 Functional Loss SNV dbSNP153 33..33 33 - - - 95776 RMVar_ID_95776 Human_SNP_ID_419200706 m1A Human chr10 - 1592193 1592193 1592193 CGGAGGAGGAGCTGGGCTTTGTTATACTTGCGAGGGCATCTGAGCTTATTATTGTCATCAAAAGC CGGAGGAGGAGCTGGGCTTTGTTATACTTGCGGGGGCATCTGAGCTTATTATTGTCATCAAAAGC T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1592191..1592321 26863196 MeRIP-seq:(Medium) rs1452595823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2204073 95777 RMVar_ID_95777 Human_SNP_ID_419200736 m1A Human chr10 - 1592259 1592259 1592259 AGAGAGGAGACCTACAGAGTGTGGCTTGGGCCAGGGGAGCTGGGTGACAGAGGGGATCATGTGGC AGAGAGGAGACCTACAGAGTGTGGCTTGGGCCGGGGGAGCTGGGTGACAGAGGGGATCATGTGGC T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1592112..1592325 26863196 MeRIP-seq:(Medium) rs909832529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8330787 95778 RMVar_ID_95778 Human_SNP_ID_419200891 m1A Human chr10 + 1592579 1592516 1592579 ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT _________________________________AAGCCACCCTCCATAGGTCTCCTCTCTGGCAT CAAGCCACCCTCCATAGGTCTCCTCTCTGGCATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1592536..1592620 26863196 MeRIP-seq:(Medium) rs869028771 Functional Loss DEL dbSNP153 1..33 33 - - - 95779 RMVar_ID_95779 Human_SNP_ID_419200905 m1A Human chr10 + 1592580 1592568 1592601 TGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCATG TGGTCCCCTCTGTCACCCAGATTCACTCACCCAAGCCACCCTCCATAGGTCTCTTCTCTGGCATG CTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCC ATTCACTCACCCAAGCCACCCTCCATAGGTCTCT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1592526..1592628 26863196 MeRIP-seq:(Medium) rs1554774182 Functional Loss MNV dbSNP153 21..54 33 - - - 95780 RMVar_ID_95780 Human_SNP_ID_419200905 m1A Human chr10 + 1592579 1592568 1592601 ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT ATGGTCCCCTCTGTCACCCAGATTCACTCACCCAAGCCACCCTCCATAGGTCTCTTCTCTGGCAT CTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCC ATTCACTCACCCAAGCCACCCTCCATAGGTCTCT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1592536..1592620 26863196 MeRIP-seq:(Medium) rs1554774182 Functional Loss MNV dbSNP153 22..55 33 - - - 95781 RMVar_ID_95781 Human_SNP_ID_419200915 m1A Human chr10 + 1592579 1592579 1592579 ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCCAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1592536..1592620 26863196 MeRIP-seq:(Medium) rs34546595 Functional Loss SNV dbSNP153 33..33 33 - - - 95782 RMVar_ID_95782 Human_SNP_ID_419200916 m1A Human chr10 + 1592580 1592580 1592580 TGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCATG TGGTCCCCTCTGTCACCCAGCTCCCTTCGCCATAGCCACCCTCCATAGGTCTCCTCTCTGGCATG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1592526..1592628 26863196 MeRIP-seq:(Medium) rs1164162193 Functional Loss SNV dbSNP153 33..33 33 - - - 95783 RMVar_ID_95783 Human_SNP_ID_419200981 m1A Human chr10 + 1592761 1592761 1592761 CTCTGGCATGGTCCCCTCTGTCACCCAGATTCACTCACCCAAGCCACCCTCCATAGGTCTCTTCT CTCTGGCATGGTCCCCTCTGTCACCCAGATTCCCTCACCCAAGCCACCCTCCATAGGTCTCTTCT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1592673..1592859;chr10:1592701..1592900 26863196 MeRIP-seq:(Medium) rs1564341219 Functional Loss SNV dbSNP153 33..33 33 - - - 95784 RMVar_ID_95784 Human_SNP_ID_419201079 m1A Human chr10 - 1593043 1593043 1593043 GAAGCTGGGTGACAGAGGGGACCATGCCAGAGAGGAGACCTATGGAGGGTGGCTTGGGTGAGGGA GAAGCTGGGTGACAGAGGGGACCATGCCAGAGGGGAGACCTATGGAGGGTGGCTTGGGTGAGGGA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1593036..1593185 26863196 MeRIP-seq:(Medium) rs112885196 Functional Loss SNV dbSNP153 33..33 33 - - - 95785 RMVar_ID_95785 Human_SNP_ID_419201087 m1A Human chr10 + 1593084 1593084 1593084 TGGTCCCCTCTGTCACCCAGCTTCCCTCGCCCACGCCACCCTCCATAGGTCTCCTCTCTGGCATG TGGTCCCCTCTGTCACCCAGCTTCCCTCGCCCCCGCCACCCTCCATAGGTCTCCTCTCTGGCATG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:1593026..1593225 26863196 MeRIP-seq:(Medium) rs1334944303 Functional Loss SNV dbSNP153 33..33 33 - - - 95786 RMVar_ID_95786 Human_SNP_ID_419201188 m1A Human chr10 + 1593318 1593302 1593318 TAGGTCTCCTCTCTGGCATGGTCCCCTCTGTCACCCAGCTCCCCTGGCCCAAACCACACTCTGTA TAGGTCTCCTCTCTGGC________________CCCAGCTCCCCTGGCCCAAACCACACTCTGTA CATGGTCCCCTCTGTCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1593292..1593440 26863196 MeRIP-seq:(Medium) rs1255973745 Functional Loss DEL dbSNP153 18..33 33 - - - 95787 RMVar_ID_95787 Human_SNP_ID_419204578 m1A Human chr10 - 1605313 1605313 1605313 TGTCACAGTAAGAGCTGCGTGGAATCACAAGAACCTGATTGCATCAGTGACCAGCAAACCCTCAG TGTCACAGTAAGAGCTGCGTGGAATCACAAGAGCCTGATTGCATCAGTGACCAGCAAACCCTCAG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1605306..1605407 26863196 MeRIP-seq:(Medium) rs1396215411 Functional Loss SNV dbSNP153 33..33 33 - - - 95788 RMVar_ID_95788 Human_SNP_ID_419210399 m1A Human chr10 - 1625818 1625818 1625818 CAGGAGGCATGGCTGTGCTGGGTGATGAGGACATGGGAAGGCCACAGCTCAGCAGGAGAAGGGTG CAGGAGGCATGGCTGTGCTGGGTGATGAGGACGTGGGAAGGCCACAGCTCAGCAGGAGAAGGGTG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1625791..1626527 26863196 MeRIP-seq:(Medium) rs1427439315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2205030 95789 RMVar_ID_95789 Human_SNP_ID_419210445 m1A Human chr10 + 1625929 1625922 1625929 CTCTGCCTGACCCTGCGCTCTCTCCTGCATGGACACAGGCCTCCAGTGGACCTCGGATGCTAACC CTCTGCCTGACCCTGCGCTCTCTCCT_______CACAGGCCTCCAGTGGACCTCGGATGCTAACC TGCATGGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1625696..1626681 26863196 MeRIP-seq:(Medium) rs1250664906 Functional Loss DEL dbSNP153 27..33 33 - - - 95790 RMVar_ID_95790 Human_SNP_ID_419210871 m1A Human chr10 + 1626950 1626950 1626950 CATCAGCACCCACCCTGTGCCTTCCTCCTAAGAATCCCTCTCTGTGGGGTCCTGCTGCCCTCTCC CATCAGCACCCACCCTGTGCCTTCCTCCTAAGGATCCCTCTCTGTGGGGTCCTGCTGCCCTCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1626948..1627064 26863196 MeRIP-seq:(Medium) rs1384948727 Functional Loss SNV dbSNP153 33..33 33 - - - 95791 RMVar_ID_95791 Human_SNP_ID_419214500 m1A Human chr10 - 1638875 1638875 1638875 CTTGTGTCACCTGCATGGAGGGAGCACGGATGAGAAGTATGTGAGCCCCCGACACACCATTTTAA CTTGTGTCACCTGCATGGAGGGAGCACGGATGGGAAGTATGTGAGCCCCCGACACACCATTTTAA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:1638790..1638975 26863196 MeRIP-seq:(Medium) rs1385485161 Functional Loss SNV dbSNP153 33..33 33 - - - 95792 RMVar_ID_95792 Human_SNP_ID_419215596 m1A Human chr10 + 1642745 1642745 1642745 ACTCACACATTTACCCACAAACTCACATCCACACTCACATGCACACACACTCACACTCCCTCACT ACTCACACATTTACCCACAAACTCACATCCACCCTCACATGCACACACACTCACACTCCCTCACT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1642661..1642900 26863196 MeRIP-seq:(Medium) rs1183245611 Functional Loss SNV dbSNP153 33..33 33 - - - 95793 RMVar_ID_95793 Human_SNP_ID_419218949 m1A Human chr10 + 1653593 1653591 1653593 CTCCACCCCACGCCTCATGTGCCTGCAGAGCCACAGTCTCCACCCAACGCCTTCTGTGCCTGCAG CTCCACCCCACGCCTCATGTGCCTGCAGAGC__CAGTCTCCACCCAACGCCTTCTGTGCCTGCAG CCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1653584..1653650 26863196 MeRIP-seq:(Medium) rs1187873721 Functional Loss DEL dbSNP153 32..33 33 - - - 95794 RMVar_ID_95794 Human_SNP_ID_419218952 m1A Human chr10 + 1653593 1653593 1653593 CTCCACCCCACGCCTCATGTGCCTGCAGAGCCACAGTCTCCACCCAACGCCTTCTGTGCCTGCAG CTCCACCCCACGCCTCATGTGCCTGCAGAGCCGCAGTCTCCACCCAACGCCTTCTGTGCCTGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1653584..1653650 26863196 MeRIP-seq:(Medium) rs1417011293 Functional Loss SNV dbSNP153 33..33 33 - - - 95795 RMVar_ID_95795 Human_SNP_ID_419220165 m1A Human chr10 - 1657938 1657935 1657939 AGAGACTGAGGCAGACACAGACAGAGAATCAGATAAAGAGAGACAGAGAATCAGATAAAGAGAGA AGAGACTGAGGCAGACACAGACAGAGAATCA____AAGAGAGACAGAGAATCAGATAAAGAGAGA TTATC T ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1657776..1658610 26863196 MeRIP-seq:(Medium) rs1300298609 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5545443 95796 RMVar_ID_95796 Human_SNP_ID_419220223 m1A Human chr10 - 1658073 1658073 1658073 ACAGAGAGAGAGAATCAGACAGAGAGACACAGAGACACAGAGAGAGACAGTAGAGACAGAAGAGA ACAGAGAGAGAGAATCAGACAGAGAGACACAGCGACACAGAGAGAGACAGTAGAGACAGAAGAGA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:1657992..1658300 26863196 MeRIP-seq:(Medium) rs934012374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2206266,Human_RBP_ID_5545447 95797 RMVar_ID_95797 Human_SNP_ID_419220276 m1A Human chr10 - 1658217 1658217 1658217 AGACATACAGAGAGAGAGAGAATCAGATAGAGACAGAGAGAGACAGAAAAAGACAATCAGATAGA AGACATACAGAGAGAGAGAGAATCAGATAGAGCCAGAGAGAGACAGAAAAAGACAATCAGATAGA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:1658101..1658481 26863196 MeRIP-seq:(Medium) rs1013914886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5545452 95798 RMVar_ID_95798 Human_SNP_ID_419220874 m1A Human chr10 - 1659987 1659987 1659987 GGGGTCTCACAGGACAGTGGAGGAGAGGAAGGAAGGCAGGCAGATGAACCCAGAAGCAGCATGAT GGGGTCTCACAGGACAGTGGAGGAGAGGAAGGCAGGCAGGCAGATGAACCCAGAAGCAGCATGAT T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1659957..1660164 26863196 MeRIP-seq:(Medium) rs1284431281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2206311 95799 RMVar_ID_95799 Human_SNP_ID_419220881 m1A Human chr10 - 1660004 1660004 1660004 GAGACAGCCCCTGCCCCGGGGTCTCACAGGACAGTGGAGGAGAGGAAGGAAGGCAGGCAGATGAA GAGACAGCCCCTGCCCCGGGGTCTCACAGGACGGTGGAGGAGAGGAAGGAAGGCAGGCAGATGAA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1659953..1660162 26863196 MeRIP-seq:(Medium) rs780874746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2206311 95800 RMVar_ID_95800 Human_SNP_ID_419220915 m1A Human chr10 - 1660090 1660090 1660090 GGAGGAGAGCAAGGAAGGCAGGCGGATGAACCAGGAAGCTGCATGATGGGTTGCCCAGGCAGGGC GGAGGAGAGCAAGGAAGGCAGGCGGATGAACCCGGAAGCTGCATGATGGGTTGCCCAGGCAGGGC T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1659838..1660183 26863196 MeRIP-seq:(Medium) rs11817851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2206314,Human_RBP_ID_11322988 95801 RMVar_ID_95801 Human_SNP_ID_419223600 m1A Human chr10 + 1669476 1669465 1669477 ACACACAAACAGGGAGACACAAACACAGACACAGACACACACACACTCACAGGGAGACACAGCTA ACACACAAACAGGGAGACACAA____________ACACACACACACTCACAGGGAGACACAGCTA AACACAGACACAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1669465..1669936 26863196 MeRIP-seq:(Medium) rs1184752700 Functional Loss DEL dbSNP153 23..34 33 - - - 95802 RMVar_ID_95802 Human_SNP_ID_419223601 m1A Human chr10 + 1669476 1669465 1669477 ACACACAAACAGGGAGACACAAACACAGACACAGACACACACACACTCACAGGGAGACACAGCTA ACACACAAACAGGGAGACACAAACACAG______ACACACACACACTCACAGGGAGACACAGCTA AACACAGACACAG AACACAG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1669465..1669936 26863196 MeRIP-seq:(Medium) rs1184752700 Functional Loss DEL dbSNP153 29..34 33 - - - 95803 RMVar_ID_95803 Human_SNP_ID_419223636 m1A Human chr10 + 1669546 1669546 1669546 ACAGACACACTCACAGAGAAAAACACAGGCACACTCAGAGAGACACACACAGACACAAACACACA ACAGACACACTCACAGAGAAAAACACAGGCACGCTCAGAGAGACACACACAGACACAAACACACA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:1669502..1669827 26863196 MeRIP-seq:(Medium) rs1372270730 Functional Loss SNV dbSNP153 33..33 33 - - - 95804 RMVar_ID_95804 Human_SNP_ID_419223638 m1A Human chr10 - 1669548 1669548 1669548 TCTGTGTGTTTGTGTCTGTGTGTGTCTCTCTGAGTGTGCCTGTGTTTTTCTCTGTGAGTGTGTCT TCTGTGTGTTTGTGTCTGTGTGTGTCTCTCTGTGTGTGCCTGTGTTTTTCTCTGTGAGTGTGTCT T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr10:1669501..1669975;chr10:1669520..1669666 26863196 MeRIP-seq:(Medium) rs1329914432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2206680 95805 RMVar_ID_95805 Human_SNP_ID_419223738 m1A Human chr10 - 1669796 1669796 1669796 TGTGAGTCTATGTGTCTGTGTTTGTCTCTGTGACTGTGTCTGTGTGTTTGTGTCTGTGTGTTTTT TGTGAGTCTATGTGTCTGTGTTTGTCTCTGTGTCTGTGTCTGTGTGTTTGTGTCTGTGTGTTTTT T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:1669451..1669950 26863196 MeRIP-seq:(Medium) rs1267213087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23447597 95806 RMVar_ID_95806 Human_SNP_ID_419223763 m1A Human chr10 + 1669872 1669871 1669873 AGACACACTCATAGAGACACACAGACACAAATACACACAGACACACTCACCAAGACAAACACAGA AGACACACTCATAGAGACACACAGACACAAAT__ACACAGACACACTCACCAAGACAAACACAGA TAC T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1669401..1669975 26863196 MeRIP-seq:(Medium) rs1278638218 Functional Loss DEL dbSNP153 33..34 33 - - - 95807 RMVar_ID_95807 Human_SNP_ID_419223765 m1A Human chr10 + 1669872 1669872 1669872 AGACACACTCATAGAGACACACAGACACAAATACACACAGACACACTCACCAAGACAAACACAGA AGACACACTCATAGAGACACACAGACACAAATTCACACAGACACACTCACCAAGACAAACACAGA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1669401..1669975 26863196 MeRIP-seq:(Medium) rs1386282672 Functional Loss SNV dbSNP153 33..33 33 - - - 95808 RMVar_ID_95808 Human_SNP_ID_419224605 m1A Human chr10 - 1672616 1672603 1672617 CCTGCAAGGAGGAGGGGAAAGTGTGTCCATGGAGGGAGGCAGGCGCGGGGCTTGGAGGGAGGAAG CCTGCAAGGAGGAGGGGAAAGTGTGTCCATG______________CGGGGCTTGGAGGGAGGAAG GCGCCTGCCTCCCTC G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1672503..1672771 26863196 MeRIP-seq:(Medium) rs1268999442 Functional Loss DEL dbSNP153 32..45 33 - - - 95809 RMVar_ID_95809 Human_SNP_ID_419224672 m1A Human chr10 - 1672698 1672682 1672708 CGGTGCGTGGAGGAGGCAGGCGGGGGGCCTGGAAGGAGGAAAGGGAAGTGCGTGCGTGGAGGGAG CGGTGCGTGGAGGAGGCAGGCGCGGGGCCTGGACGGAGGAGGGGGAAGCGCGTGCGTGGAGGGAG ACTTCCCTTTCCTCCTTCCAGGCCCCC GCTTCCCCCTCCTCCGTCCAGGCCCCG ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1672501..1672750 26863196 MeRIP-seq:(Medium) rs386739882 Functional Loss MNV dbSNP153 23..49 33 - - - Human_RBP_ID_2206792 95810 RMVar_ID_95810 Human_SNP_ID_419224672 m1A Human chr10 + 1672701 1672682 1672708 CCTCCACGCACGCACTTCCCTTTCCTCCTTCCAGGCCCCCCGCCTGCCTCCTCCACGCACCGCAA CCTCCACGCACGCGCTTCCCCCTCCTCCGTCCAGGCCCCGCGCCTGCCTCCTCCACGCACCGCAA ACTTCCCTTTCCTCCTTCCAGGCCCCC GCTTCCCCCTCCTCCGTCCAGGCCCCG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1672497..1672815 26863196 MeRIP-seq:(Medium) rs386739882 Functional Loss MNV dbSNP153 14..40 33 - - - 95811 RMVar_ID_95811 Human_SNP_ID_419224691 m1A Human chr10 + 1672701 1672701 1672701 CCTCCACGCACGCACTTCCCTTTCCTCCTTCCAGGCCCCCCGCCTGCCTCCTCCACGCACCGCAA CCTCCACGCACGCACTTCCCTTTCCTCCTTCCGGGCCCCCCGCCTGCCTCCTCCACGCACCGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1672497..1672815 26863196 MeRIP-seq:(Medium) rs1168256996 Functional Loss SNV dbSNP153 33..33 33 - - - 95812 RMVar_ID_95812 Human_SNP_ID_419225419 m1A Human chr10 + 1674957 1674957 1674957 TGGATGTTCTGGAGGTTTGGGTTTGGGGGTACACGGATATTCTGGAGGTTTGGGTTTGGGGGGTA TGGATGTTCTGGAGGTTTGGGTTTGGGGGTACCCGGATATTCTGGAGGTTTGGGTTTGGGGGGTA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1674906..1675184 26863196 MeRIP-seq:(Medium) rs1450449243 Functional Loss SNV dbSNP153 33..33 33 - - - 95813 RMVar_ID_95813 Human_SNP_ID_419225427 m1A Human chr10 - 1674974 1674970 1674974 CCTCCAGAATATCCATGTACCCCCCAAACCCAAACCTCCAGAATATCCGTGTACCCCCAAACCCA CCTCCAGAATATCCATGTACCCCCCAAACCCA____TCCAGAATATCCGTGTACCCCCAAACCCA AGGTT A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:1674924..1675109 26863196 MeRIP-seq:(Medium) rs1182207877 Functional Loss DEL dbSNP153 33..36 33 - - - 95814 RMVar_ID_95814 Human_SNP_ID_419225703 m1A Human chr10 + 1675528 1675528 1675528 GGAGGTTTGGGTTTGGGGATGCGTGGATGTTCAGGAGGTTTGGGTTTGGGGGTACATGGATGTTC GGAGGTTTGGGTTTGGGGATGCGTGGATGTTCTGGAGGTTTGGGTTTGGGGGTACATGGATGTTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1675350..1675683 26863196 MeRIP-seq:(Medium) rs77814469 Functional Loss SNV dbSNP153 33..33 33 - - - 95815 RMVar_ID_95815 Human_SNP_ID_419230862 m1A Human chr10 - 1694825 1694825 1694825 TTTGCTGTGAGTCATGAAGACCCCACTCCCAGACATCTGCTCATCCTAACCCCATAACCCTCCCT TTTGCTGTGAGTCATGAAGACCCCACTCCCAGGCATCTGCTCATCCTAACCCCATAACCCTCCCT T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:1694776..1694920 26863196 MeRIP-seq:(Medium) rs1391958630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2207674 95816 RMVar_ID_95816 Human_SNP_ID_419237046 m1A Human chr10 - 1716021 1716021 1716021 GTCGTGATGGAACGCGCAGGGCACACTGACTCAGCGGGCGGGAGGGGAGTGTGCATACAGCAGCT GTCGTGATGGAACGCGCAGGGCACACTGACTCGGCGGGCGGGAGGGGAGTGTGCATACAGCAGCT T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1715990..1716074 26863196 MeRIP-seq:(Medium) rs1213716415 Functional Loss SNV dbSNP153 33..33 33 - - - 95817 RMVar_ID_95817 Human_SNP_ID_419243052 m1A Human chr10 - 1737081 1737081 1737081 GGCTGAGCAGTCAACTCAAATGCAAGTCCAAGAGGAGGAGGAGGCGGAGGTCCAAGCGGAAAGGT GGCTGAGCAGTCAACTCAAATGCAAGTCCAAGGGGAGGAGGAGGCGGAGGTCCAAGCGGAAAGGT T C ADARB2 Ensembl:ENSG00000185736 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:1737060..1737476 26863196 MeRIP-seq:(Medium) rs779764730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5545578 Human_Splice_Rec_1106823 95818 RMVar_ID_95818 Human_SNP_ID_419243186 m1A Human chr10 - 1737388 1737388 1737388 ACGCCGCGCGCCCTTCCCCGCCCTCCCTGACCAGGGAGCAGCTCGCTCCAGGCGCCCAGCCGAGG ACGCCGCGCGCCCTTCCCCGCCCTCCCTGACCCGGGAGCAGCTCGCTCCAGGCGCCCAGCCGAGG T G ADARB2 Ensembl:ENSG00000185736 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1737340..1737482 26863196 MeRIP-seq:(Medium) rs936315383 Functional Loss SNV dbSNP153 33..33 33 - - - 95819 RMVar_ID_95819 Human_SNP_ID_419626837 m1A Human chr10 + 3067600 3067600 3067600 ACGTGCGGCTCCCCTCGGCCTCCTCGCCATGGACGCGGACGACTCCCGGGCCCCCAAGGGCTCCT ACGTGCGGCTCCCCTCGGCCTCCTCGCCATGGTCGCGGACGACTCCCGGGCCCCCAAGGGCTCCT A T PFKP Ensembl:ENSG00000067057 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:3067501..3067725 26863410 MeRIP-seq:(Medium) rs1023552134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_104368,Human_RBP_ID_4136126,Human_RBP_ID_8765531,Human_RBP_ID_17775999 RMVar_hsa_circ_123596,RMVar_hsa_circ_141625 95820 RMVar_ID_95820 Human_SNP_ID_419626899 m1A Human chr10 + 3067705 3067705 3067705 CATCGGCGTGCTGACCAGCGGCGGGGATGCTCAAGGTGCGCGCCCCCCTCCCGGCGGCGAGGGAG CATCGGCGTGCTGACCAGCGGCGGGGATGCTCTAGGTGCGCGCCCCCCTCCCGGCGGCGAGGGAG A T PFKP Ensembl:ENSG00000067057 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3067552..3067942 26863196 MeRIP-seq:(Medium) rs548170125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_104368 Human_Splice_Rec_1107047,Human_Splice_Rec_1107089 RMVar_hsa_circ_123596,RMVar_hsa_circ_141625 95821 RMVar_ID_95821 Human_SNP_ID_419626900 m1A Human chr10 - 3067709 3067709 3067709 GTCCCTCCCTCGCCGCCGGGAGGGGGGCGCGCACCTTGAGCATCCCCGCCGCTGGTCAGCACGCC GTCCCTCCCTCGCCGCCGGGAGGGGGGCGCGCCCCTTGAGCATCCCCGCCGCTGGTCAGCACGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:3067666..3067797 26863196 MeRIP-seq:(Medium) rs1024670604 Functional Loss SNV dbSNP153 33..33 33 - - - 95822 RMVar_ID_95822 Human_SNP_ID_419627184 m1A Human chr10 + 3068459 3068459 3068459 TCGTGACAAAAACGAAAACCAAAATGGGTCCCAGGCCCTCCCCGCCAGCCTCCGCAGACGGGAAG TCGTGACAAAAACGAAAACCAAAATGGGTCCCGGGCCCTCCCCGCCAGCCTCCGCAGACGGGAAG A G PFKP Ensembl:ENSG00000067057 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:3068456..3068675 26863196 MeRIP-seq:(Medium) rs985071189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123596,RMVar_hsa_circ_141625 95823 RMVar_ID_95823 Human_SNP_ID_419631315 m1A Human chr10 + 3080807 3080807 3080807 CTTCTGGCCACAGTGTGGCTCATGTCAGAGGGAGTCAGGGAGTCGGGGGTAATGTTGGGAGCAGG CTTCTGGCCACAGTGTGGCTCATGTCAGAGGGTGTCAGGGAGTCGGGGGTAATGTTGGGAGCAGG A T PFKP Ensembl:ENSG00000067057 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:3080803..3080953 26863196 MeRIP-seq:(Medium) rs973046976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12785,RMVar_hsa_circ_123596,RMVar_hsa_circ_80951,RMVar_hsa_circ_141625,RMVar_hsa_circ_141626 95824 RMVar_ID_95824 Human_SNP_ID_419631948 m1A Human chr10 - 3082463 3082463 3082463 GAAGGGCGACAGGGGGTGAGGGGCAGACACTGACCTCGTAGATGAAGTACACCTTGGCCCCCACG GAAGGGCGACAGGGGGTGAGGGGCAGACACTGCCCTCGTAGATGAAGTACACCTTGGCCCCCACG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:3082413..3099327 32194978 MeRIP-seq:(Medium) rs765348848 Functional Loss SNV dbSNP153 33..33 33 - - - 95825 RMVar_ID_95825 Human_SNP_ID_419638168 m1A Human chr10 - 3099226 3099225 3099226 GAATCTTTTAAAAATGAGATAAACTTCACTAAATGGGAAGTGATCCTTAAATTATATAAAACGGG GAATCTTTTAAAAATGAGATAAACTTCACTAA_TGGGAAGTGATCCTTAAATTATATAAAACGGG AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3099220..3099392 26863196 MeRIP-seq:(Medium) rs765881026 Functional Loss DEL dbSNP153 33..33 33 - - - 95826 RMVar_ID_95826 Human_SNP_ID_419639176 m1A Human chr10 + 3101488 3101488 3101488 TCACCAACCTGTGTGTGATCGGCGGGGACGGGAGCCTCACCGGGGCCAACCTCTTCCGGAAGGAG TCACCAACCTGTGTGTGATCGGCGGGGACGGGGGCCTCACCGGGGCCAACCTCTTCCGGAAGGAG A G PFKP Ensembl:ENSG00000067057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3101351..3101550 32194978 MeRIP-seq:(Medium) rs753934996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26270 Human_Splice_Rec_1107053,Human_Splice_Rec_1107101,Human_Splice_Rec_1107143,Human_Splice_Rec_1107151 Human_miRNA_ID_1967224,Human_miRNA_ID_1967225 RMVar_hsa_circ_10002,RMVar_hsa_circ_12785,RMVar_hsa_circ_123596,RMVar_hsa_circ_80951,RMVar_hsa_circ_141625,RMVar_hsa_circ_141627,RMVar_hsa_circ_313987,RMVar_hsa_circ_141626,RMVar_hsa_circ_335809,RMVar_hsa_circ_141628,RMVar_hsa_circ_103167,RMVar_hsa_circ_110330,RMVar_hsa_circ_22061,RMVar_hsa_circ_82384,RMVar_hsa_circ_141630,RMVar_hsa_circ_141631,RMVar_hsa_circ_141629,RMVar_hsa_circ_319639,RMVar_hsa_circ_141632,RMVar_hsa_circ_141633 95827 RMVar_ID_95827 Human_SNP_ID_419641832 m1A Human chr10 + 3107308 3107308 3107308 AAATAAACCCATCACCTCTGAGAAAATCAAAGAGGTGAGTGTGTGTAGCTGCTCACTTTCTCTCG AAATAAACCCATCACCTCTGAGAAAATCAAAGGGGTGAGTGTGTGTAGCTGCTCACTTTCTCTCG A G PFKP Ensembl:ENSG00000067057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3107276..3107325 32194978 MeRIP-seq:(Medium) rs1399669536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1107060,Human_Splice_Rec_1107061,Human_Splice_Rec_1107108,Human_Splice_Rec_1107109,Human_Splice_Rec_1107160,Human_Splice_Rec_1107161,Human_Splice_Rec_1107194,Human_Splice_Rec_1107195,Human_Splice_Rec_1107202 RMVar_hsa_circ_12785,RMVar_hsa_circ_123596,RMVar_hsa_circ_80951,RMVar_hsa_circ_141625,RMVar_hsa_circ_141627,RMVar_hsa_circ_313987,RMVar_hsa_circ_141626,RMVar_hsa_circ_335809,RMVar_hsa_circ_141628,RMVar_hsa_circ_103167,RMVar_hsa_circ_110330,RMVar_hsa_circ_22061,RMVar_hsa_circ_19081,RMVar_hsa_circ_49909,RMVar_hsa_circ_82384,RMVar_hsa_circ_141630,RMVar_hsa_circ_141631,RMVar_hsa_circ_141629,RMVar_hsa_circ_319639,RMVar_hsa_circ_141632,RMVar_hsa_circ_141633,RMVar_hsa_circ_114970,RMVar_hsa_circ_16279,RMVar_hsa_circ_96011,RMVar_hsa_circ_117639,RMVar_hsa_circ_141634,RMVar_hsa_circ_25485,RMVar_hsa_circ_21901,RMVar_hsa_circ_122586,RMVar_hsa_circ_141635,RMVar_hsa_circ_141636,RMVar_hsa_circ_124457,RMVar_hsa_circ_356140,RMVar_hsa_circ_79370,RMVar_hsa_circ_115451,RMVar_hsa_circ_49595,RMVar_hsa_circ_141638,RMVar_hsa_circ_141639,RMVar_hsa_circ_141640,RMVar_hsa_circ_369620,RMVar_hsa_circ_141637,RMVar_hsa_circ_141641 95828 RMVar_ID_95828 Human_SNP_ID_419642328 m1A Human chr10 + 3108726 3108725 3108727 CTTGCAGCTTGTCGTCACGCAGCTGGGCTATGACACACGTGTGACCATCCTCGGGCACGTGCAGA CTTGCAGCTTGTCGTCACGCAGCTGGGCTATG__ACACGTGTGACCATCCTCGGGCACGTGCAGA GAC G PFKP Ensembl:ENSG00000067057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3108701..3108725 32194978 MeRIP-seq:(Medium) rs1346192758 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26280,Human_RBP_ID_8765221,Human_RBP_ID_22639107,Human_RBP_ID_23452917 Human_Splice_Rec_1107062,Human_Splice_Rec_1107063,Human_Splice_Rec_1107110,Human_Splice_Rec_1107111,Human_Splice_Rec_1107162,Human_Splice_Rec_1107163,Human_Splice_Rec_1107196,Human_Splice_Rec_1107197 Human_miRNA_ID_1956968,Human_miRNA_ID_1956969,Human_miRNA_ID_2466538,Human_miRNA_ID_2466539 RMVar_hsa_circ_12785,RMVar_hsa_circ_123596,RMVar_hsa_circ_80951,RMVar_hsa_circ_141625,RMVar_hsa_circ_141627,RMVar_hsa_circ_313987,RMVar_hsa_circ_141626,RMVar_hsa_circ_335809,RMVar_hsa_circ_141628,RMVar_hsa_circ_103167,RMVar_hsa_circ_110330,RMVar_hsa_circ_22061,RMVar_hsa_circ_19081,RMVar_hsa_circ_49909,RMVar_hsa_circ_82384,RMVar_hsa_circ_141630,RMVar_hsa_circ_141631,RMVar_hsa_circ_141629,RMVar_hsa_circ_319639,RMVar_hsa_circ_141632,RMVar_hsa_circ_141633,RMVar_hsa_circ_114970,RMVar_hsa_circ_16279,RMVar_hsa_circ_96011,RMVar_hsa_circ_117639,RMVar_hsa_circ_141634,RMVar_hsa_circ_25485,RMVar_hsa_circ_21901,RMVar_hsa_circ_122586,RMVar_hsa_circ_141635,RMVar_hsa_circ_141636,RMVar_hsa_circ_124457,RMVar_hsa_circ_356140,RMVar_hsa_circ_79370,RMVar_hsa_circ_115451,RMVar_hsa_circ_49595,RMVar_hsa_circ_123468,RMVar_hsa_circ_141638,RMVar_hsa_circ_141639,RMVar_hsa_circ_141640,RMVar_hsa_circ_369620,RMVar_hsa_circ_141637,RMVar_hsa_circ_141641,RMVar_hsa_circ_141643,RMVar_hsa_circ_121370,RMVar_hsa_circ_141642 95829 RMVar_ID_95829 Human_SNP_ID_419642774 m1A Human chr10 - 3109819 3109819 3109819 CACGGATCTCTCTCTCTCGGCTGCCTCCCTGCACTCTGTCCTTCTGCAGCACCTGGTGCACTGGG CACGGATCTCTCTCTCTCGGCTGCCTCCCTGCGCTCTGTCCTTCTGCAGCACCTGGTGCACTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:3109815..3109926 26863196 MeRIP-seq:(Medium) rs1158664217 Functional Loss SNV dbSNP153 33..33 33 - - - 95830 RMVar_ID_95830 Human_SNP_ID_419644078 m1A Human chr10 - 3113071 3113071 3113071 GTCGTTGGACCGGAGTCGAGAATACCGGACACAACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA GTCGTTGGACCGGAGTCGAGAATACCGGACACGACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3113068..3113235 26863196 MeRIP-seq:(Medium) rs7906901 Functional Loss SNV dbSNP153 33..33 33 - - - 95831 RMVar_ID_95831 Human_SNP_ID_419644079 m1A Human chr10 - 3113071 3113071 3113072 GTCGTTGGACCGGAGTCGAGAATACCGGACACAACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA GTCGTTGGACCGGAGTCGAGAATACCGGACAAGACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA TG CT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3113068..3113235 26863196 MeRIP-seq:(Medium) rs796153288 Functional Loss MNV dbSNP153 32..33 33 - - - 95832 RMVar_ID_95832 Human_SNP_ID_419645138 m1A Human chr10 - 3115405 3115405 3115405 GTCCTGTCCTCCATGGCGGGACACACACCTTCACCCCGGCATCCCCAGTCCTGTTCTCAGCTGCG GTCCTGTCCTCCATGGCGGGACACACACCTTCGCCCCGGCATCCCCAGTCCTGTTCTCAGCTGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:3115393..3115632 26863196 MeRIP-seq:(Medium) rs572178286 Functional Loss SNV dbSNP153 33..33 33 - - - 95833 RMVar_ID_95833 Human_SNP_ID_419645753 m1A Human chr10 - 3116853 3116853 3116853 CCTTAAAAGCAGGTCATAGAGTTGAGATTTGGAAGTTACCGTTTTGTCCCAAGAATGGAGCCTCC CCTTAAAAGCAGGTCATAGAGTTGAGATTTGGCAGTTACCGTTTTGTCCCAAGAATGGAGCCTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3116851..3116875 32194978 MeRIP-seq:(Medium) rs753583374 Functional Loss SNV dbSNP153 33..33 33 - - - 95834 RMVar_ID_95834 Human_SNP_ID_419650770 m1A Human chr10 - 3129805 3129800 3129805 GCTTGATGCGGTCGCAGGTCTGGTCACAGAGAAGCGATCAGTCACTCCAGCCCAGGCCCGGGGCG GCTTGATGCGGTCGCAGGTCTGGTCACAGAGA_____TCAGTCACTCCAGCCCAGGCCCGGGGCG ATCGCT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3129801..3129900 32194978 MeRIP-seq:(Medium) rs778941008 Functional Loss DEL dbSNP153 33..37 33 - - - 95835 RMVar_ID_95835 Human_SNP_ID_419650772 m1A Human chr10 - 3129805 3129802 3129805 GCTTGATGCGGTCGCAGGTCTGGTCACAGAGAAGCGATCAGTCACTCCAGCCCAGGCCCGGGGCG GCTTGATGCGGTCGCAGGTCTGGTCACAGAGA___GATCAGTCACTCCAGCCCAGGCCCGGGGCG CGCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3129801..3129900 32194978 MeRIP-seq:(Medium) rs1564352319 Functional Loss DEL dbSNP153 33..35 33 - - - 95836 RMVar_ID_95836 Human_SNP_ID_419650778 m1A Human chr10 - 3129805 3129805 3129805 GCTTGATGCGGTCGCAGGTCTGGTCACAGAGAAGCGATCAGTCACTCCAGCCCAGGCCCGGGGCG GCTTGATGCGGTCGCAGGTCTGGTCACAGAGACGCGATCAGTCACTCCAGCCCAGGCCCGGGGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3129801..3129900 32194978 MeRIP-seq:(Medium) rs769727920 Functional Loss SNV dbSNP153 33..33 33 - - - 95837 RMVar_ID_95837 Human_SNP_ID_419650885 m1A Human chr10 + 3129976 3129976 3129976 ATACATTTTCGAAGAGCCCTTCGACATCAGGGATCTGCAGGTATGTGACGGGGCTGGCCTCAGGG ATACATTTTCGAAGAGCCCTTCGACATCAGGGGTCTGCAGGTATGTGACGGGGCTGGCCTCAGGG A G PFKP Ensembl:ENSG00000067057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3129815..3130007 26863196 MeRIP-seq:(Medium) rs758320458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17786661,Human_RBP_ID_22029125 Human_Splice_Rec_1107079,Human_Splice_Rec_1107127,Human_Splice_Rec_1107179,Human_Splice_Rec_1107211 Human_miRNA_ID_3001313 RMVar_hsa_circ_80951,RMVar_hsa_circ_141626,RMVar_hsa_circ_103167,RMVar_hsa_circ_82384,RMVar_hsa_circ_141631,RMVar_hsa_circ_141633,RMVar_hsa_circ_114970,RMVar_hsa_circ_96011,RMVar_hsa_circ_141634,RMVar_hsa_circ_21901,RMVar_hsa_circ_141635,RMVar_hsa_circ_124457,RMVar_hsa_circ_115451,RMVar_hsa_circ_141639,RMVar_hsa_circ_141640,RMVar_hsa_circ_87230,RMVar_hsa_circ_141644,RMVar_hsa_circ_104666,RMVar_hsa_circ_15925,RMVar_hsa_circ_44997,RMVar_hsa_circ_141646,RMVar_hsa_circ_88885,RMVar_hsa_circ_291741,RMVar_hsa_circ_111313,RMVar_hsa_circ_105857,RMVar_hsa_circ_141648,RMVar_hsa_circ_141647,RMVar_hsa_circ_317257,RMVar_hsa_circ_141651,RMVar_hsa_circ_339459,RMVar_hsa_circ_141654 95838 RMVar_ID_95838 Human_SNP_ID_419651762 m1A Human chr10 - 3132350 3132350 3132350 GGACTGGAAGAGAGTATTTTGTTAATCAGACAATAAACTTCTACTAAGTACCTACTGTGTGCCAG GGACTGGAAGAGAGTATTTTGTTAATCAGACAGTAAACTTCTACTAAGTACCTACTGTGTGCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3132347..3132478 26863196 MeRIP-seq:(Medium) rs747444252 Functional Loss SNV dbSNP153 33..33 33 - - - 95839 RMVar_ID_95839 Human_SNP_ID_419652185 m1A Human chr10 - 3133277 3133277 3133277 GCATGTGACCCAGCACGTTCTTCCTGCAGTCAAACACGCCTTTGCCCTCTTCTGAATACAGCTGG GCATGTGACCCAGCACGTTCTTCCTGCAGTCATACACGCCTTTGCCCTCTTCTGAATACAGCTGG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:3133226..3133325 32194978 MeRIP-seq:(Medium) rs377691717 Functional Loss SNV dbSNP153 33..33 33 - - - 95840 RMVar_ID_95840 Human_SNP_ID_419652186 m1A Human chr10 - 3133277 3133277 3133277 GCATGTGACCCAGCACGTTCTTCCTGCAGTCAAACACGCCTTTGCCCTCTTCTGAATACAGCTGG GCATGTGACCCAGCACGTTCTTCCTGCAGTCAGACACGCCTTTGCCCTCTTCTGAATACAGCTGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:3133226..3133325 32194978 MeRIP-seq:(Medium) rs377691717 Functional Loss SNV dbSNP153 33..33 33 - - - 95841 RMVar_ID_95841 Human_SNP_ID_419652781 m1A Human chr10 - 3134530 3134530 3134530 AGTTTTGCAGTGATCCACTCCATAGCTCTGGCAGAGATTTTGGTTCCAAAGTTTCTATCAAATGG AGTTTTGCAGTGATCCACTCCATAGCTCTGGCGGAGATTTTGGTTCCAAAGTTTCTATCAAATGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:3134476..3135850 32194978 MeRIP-seq:(Medium) rs1292402655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11348802 95842 RMVar_ID_95842 Human_SNP_ID_419654046 m1A Human chr10 - 3136788 3136788 3136788 AACTAAAACAGAGGACTGTTGGAGTCATAGGCAAATGTTTAATTAATTCTGCTCATATGCACATC AACTAAAACAGAGGACTGTTGGAGTCATAGGCTAATGTTTAATTAATTCTGCTCATATGCACATC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3136776..3136800 32194978 MeRIP-seq:(Medium) rs1262171995 Functional Loss SNV dbSNP153 33..33 33 - - - 95843 RMVar_ID_95843 Human_SNP_ID_419654667 m1A Human chr10 + 3138023 3138023 3138023 TATTGTCTCGGGCTCCTGTGCAGTCGAGCGCCACGGCTGCTCATTGGATGATCCAGGATGGGTCC TATTGTCTCGGGCTCCTGTGCAGTCGAGCGCCGCGGCTGCTCATTGGATGATCCAGGATGGGTCC A G AL451164.2 Ensembl:ENSG00000278419 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:3137827..3138025 32194978 MeRIP-seq:(Medium) rs760892954 Functional Loss SNV dbSNP153 33..33 33 - - - 95844 RMVar_ID_95844 Human_SNP_ID_419666010 m1A Human chr10 - 3172655 3172655 3172655 GCGCTGGTACCCGGGAGGGGAGGGTCCAGGGCAGGCCGGAGGCGTAGGGGTCCTCGTCCCTGCGC GCGCTGGTACCCGGGAGGGGAGGGTCCAGGGCTGGCCGGAGGCGTAGGGGTCCTCGTCCCTGCGC T A PITRM1 Ensembl:ENSG00000107959 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3172651..3172751 26863196 MeRIP-seq:(Medium) rs1470737499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17776185 95845 RMVar_ID_95845 Human_SNP_ID_419828067 m1A Human chr10 + 3785057 3785033 3785057 GTTGGACGGAGCCCGCGGTCGCGAGGGCGGCGAGGCGCGCGGTGGGAGCCGGAGCCGAAAGTCTC GTTGGACGG________________________GGCGCGCGGTGGGAGCCGGAGCCGAAAGTCTC GAGCCCGCGGTCGCGAGGGCGGCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:3785015..3785247 26863196 MeRIP-seq:(Medium) rs1156332536 Functional Loss DEL dbSNP153 10..33 33 - - - 95846 RMVar_ID_95846 Human_SNP_ID_419828091 m1A Human chr10 - 3785067 3785066 3785067 GCGCTCCGGGGAGACTTTCGGCTCCGGCTCCCACCGCGCGCCTCGCCGCCCTCGCGACCGCGGGC GCGCTCCGGGGAGACTTTCGGCTCCGGCTCCC_CCGCGCGCCTCGCCGCCCTCGCGACCGCGGGC GT G KLF6 Ensembl:ENSG00000067082 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3785023..3785094 26863196 MeRIP-seq:(Medium) rs778506658 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_747030,Human_RBP_ID_4135747,Human_RBP_ID_17345564,Human_RBP_ID_22029145 RMVar_hsa_circ_81579,RMVar_hsa_circ_141683 95847 RMVar_ID_95847 Human_SNP_ID_419828093 m1A Human chr10 - 3785067 3785067 3785067 GCGCTCCGGGGAGACTTTCGGCTCCGGCTCCCACCGCGCGCCTCGCCGCCCTCGCGACCGCGGGC GCGCTCCGGGGAGACTTTCGGCTCCGGCTCCCGCCGCGCGCCTCGCCGCCCTCGCGACCGCGGGC T C KLF6 Ensembl:ENSG00000067082 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3785023..3785094 26863196 MeRIP-seq:(Medium) rs753526978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747030,Human_RBP_ID_4135747,Human_RBP_ID_17345564,Human_RBP_ID_22029145 RMVar_hsa_circ_81579,RMVar_hsa_circ_141683 95848 RMVar_ID_95848 Human_SNP_ID_419828604 m1A Human chr10 + 3785818 3785818 3785818 CGGGGCCGCCCGGTTCCCCCCCGTCCCCTTCTATGCCCGAGGCCGCCCCGTCCCCAACTGTCCCC CGGGGCCGCCCGGTTCCCCCCCGTCCCCTTCTGTGCCCGAGGCCGCCCCGTCCCCAACTGTCCCC A G lnc-PFKP-37,lnc-PFKP-37:2 RNACentral:URS0000D5DC36,RNACentral:URS0000D57730 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:3785770..3785865 26863196 MeRIP-seq:(Medium) rs915249697 Functional Loss SNV dbSNP153 33..33 33 - - - 95849 RMVar_ID_95849 Human_SNP_ID_419828665 m1A Human chr10 + 3785957 3785957 3785957 TTCTGCGCCGCTCTGTTTCCCTACATCCCCCTAGTCATCCTCTGTTCTCTAACCTTGGGGTACCC TTCTGCGCCGCTCTGTTTCCCTACATCCCCCTGGTCATCCTCTGTTCTCTAACCTTGGGGTACCC A G lnc-PFKP-37,lnc-PFKP-37:2 RNACentral:URS0000D5DC36,RNACentral:URS0000D57730 lincRNA,lincRNA exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:3785687..3786055 26863196 MeRIP-seq:(Medium) rs1033798979 Functional Loss SNV dbSNP153 33..33 33 - - - 95850 RMVar_ID_95850 Human_SNP_ID_420286660 m1A Human chr10 + 5412616 5412616 5412616 TGCAGTCCGCTGACAGGCGCTTTCTGCCTGGCAGAGGCTGGCGGGCATCGTGCCCGTCCCTGCCG TGCAGTCCGCTGACAGGCGCTTTCTGCCTGGCGGAGGCTGGCGGGCATCGTGCCCGTCCCTGCCG A G NET1 Ensembl:ENSG00000173848 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:5412587..5412669 26863410 MeRIP-seq:(Medium) rs1000229985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225961,Human_RBP_ID_4135748,Human_RBP_ID_5234715,Human_RBP_ID_5488865,Human_RBP_ID_22029149 95851 RMVar_ID_95851 Human_SNP_ID_420294508 m1A Human chr10 - 5446652 5446636 5446652 GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGCAGCCACGTGCCCATGCCTCTCGCCGCGGTGGAG GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGC________________CTCTCGCCGCGGTGGAG GGCATGGGCACGTGGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5446645..5446752 26863196 MeRIP-seq:(Medium) rs1251439711 Functional Loss DEL dbSNP153 33..48 33 - - - 95852 RMVar_ID_95852 Human_SNP_ID_420294512 m1A Human chr10 - 5446652 5446642 5446652 GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGCAGCCACGTGCCCATGCCTCTCGCCGCGGTGGAG GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGC__________CCATGCCTCTCGCCGCGGTGGAG GGCACGTGGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5446645..5446752 26863196 MeRIP-seq:(Medium) rs1486882690 Functional Loss DEL dbSNP153 33..42 33 - - - 95853 RMVar_ID_95853 Human_SNP_ID_420294518 m1A Human chr10 - 5446652 5446652 5446652 GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGCAGCCACGTGCCCATGCCTCTCGCCGCGGTGGAG GCTTTTCTTCCCAGAGCTCGGCCACCCTCGGCGGCCACGTGCCCATGCCTCTCGCCGCGGTGGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5446645..5446752 26863196 MeRIP-seq:(Medium) rs1260728127 Functional Loss SNV dbSNP153 33..33 33 - - - 95854 RMVar_ID_95854 Human_SNP_ID_420294542 m1A Human chr10 - 5446709 5446709 5446709 TTTCCAATCAATCCACACCGAGTCAGCGCTGTAGCGACGCTATGCAGAGGCACACGGGCTTTTCT TTTCCAATCAATCCACACCGAGTCAGCGCTGTGGCGACGCTATGCAGAGGCACACGGGCTTTTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:5446658..5446808 26863196 MeRIP-seq:(Medium) rs1427498027 Functional Loss SNV dbSNP153 33..33 33 - - - 95855 RMVar_ID_95855 Human_SNP_ID_420352072 m1A Human chr10 - 5652975 5652975 5652975 GGGTGAGAGCCTGCAGCTGCAACAGCTGATCGAGAGCGGCGCCTGCGTGAACCAGGTCACCGTGG GGGTGAGAGCCTGCAGCTGCAACAGCTGATCGGGAGCGGCGCCTGCGTGAACCAGGTCACCGTGG T C ASB13 Ensembl:ENSG00000196372 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:5652924..5666562 26863196 MeRIP-seq:(Medium) rs1564219025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378554,Human_RBP_ID_4142049 Human_Splice_Rec_1108604,Human_Splice_Rec_1108614,Human_Splice_Rec_1108626 RMVar_hsa_circ_307979,RMVar_hsa_circ_141736,RMVar_hsa_circ_284268,RMVar_hsa_circ_141737,RMVar_hsa_circ_328653,RMVar_hsa_circ_141738 95856 RMVar_ID_95856 Human_SNP_ID_420352081 m1A Human chr10 - 5652993 5652993 5652993 GCACGAGGCAGCCCAGCGGGGTGAGAGCCTGCAGCTGCAACAGCTGATCGAGAGCGGCGCCTGCG GCACGAGGCAGCCCAGCGGGGTGAGAGCCTGCGGCTGCAACAGCTGATCGAGAGCGGCGCCTGCG T C ASB13 Ensembl:ENSG00000196372 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:5652944..5653080 26863196 MeRIP-seq:(Medium) rs1166658625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_378554,Human_RBP_ID_4136133 Human_Splice_Rec_1108604,Human_Splice_Rec_1108614,Human_Splice_Rec_1108626 Human_miRNA_ID_1488714,Human_miRNA_ID_2012690,Human_miRNA_ID_2759066 RMVar_hsa_circ_307979,RMVar_hsa_circ_141736,RMVar_hsa_circ_284268,RMVar_hsa_circ_141737,RMVar_hsa_circ_328653,RMVar_hsa_circ_141738 95857 RMVar_ID_95857 Human_SNP_ID_420352096 m1A Human chr10 + 5653028 5653028 5653028 AGGCTCTCACCCCGCTGGGCTGCCTCGTGCACAGGGGTCCGCTCCACCCAGAAACCTGGAAAGGA AGGCTCTCACCCCGCTGGGCTGCCTCGTGCACGGGGGTCCGCTCCACCCAGAAACCTGGAAAGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5652979..5666567 26863196 MeRIP-seq:(Medium) rs142082937 Functional Loss SNV dbSNP153 33..33 33 - - - 95858 RMVar_ID_95858 Human_SNP_ID_420360291 m1A Human chr10 - 5684899 5684899 5684899 CGTCAGGGTCACGGGCAAGAGGCAACCCCGGGACGCCCGGCAGCCTGCGAGAACATGCCGACTTT CGTCAGGGTCACGGGCAAGAGGCAACCCCGGGGCGCCCGGCAGCCTGCGAGAACATGCCGACTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:5684851..5692827;chr10:5684851..5685100 26863196 MeRIP-seq:(Medium) rs981275701 Functional Loss SNV dbSNP153 33..33 33 - - - 95859 RMVar_ID_95859 Human_SNP_ID_420360321 m1A Human chr10 - 5684959 5684959 5684959 CCCCGGGGTCCTCGCCGCGGGCGCTGACAGGGACGCCGCGGCCGCCCGCGCTCTGTCTCCCGTCA CCCCGGGGTCCTCGCCGCGGGCGCTGACAGGGGCGCCGCGGCCGCCCGCGCTCTGTCTCCCGTCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:5684870..5685028 26863196 MeRIP-seq:(Medium) rs1213294242 Functional Loss SNV dbSNP153 33..33 33 - - - 95860 RMVar_ID_95860 Human_SNP_ID_420360373 m1A Human chr10 + 5685060 5685060 5685060 CGGGAGCGCGGAGCCGGCGACTGGTGCTTCCCACGTGCGCCGGTGTCGCGAGGGCCCGGGAGGAC CGGGAGCGCGGAGCCGGCGACTGGTGCTTCCCTCGTGCGCCGGTGTCGCGAGGGCCCGGGAGGAC A T TASOR2 Ensembl:ENSG00000108021 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:5684972..5685082 32194978 MeRIP-seq:(Medium) rs897350658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225147,Human_RBP_ID_4135752,Human_RBP_ID_5254863,Human_RBP_ID_5488255,Human_RBP_ID_8761268,Human_RBP_ID_9274069,Human_RBP_ID_9320801,Human_RBP_ID_18416072,Human_RBP_ID_22030198,Human_RBP_ID_22369581,Human_RBP_ID_22788199,Human_RBP_ID_24529191 RMVar_hsa_circ_93748,RMVar_hsa_circ_141739 95861 RMVar_ID_95861 Human_SNP_ID_420387569 m1A Human chr10 + 5785998 5785998 5785998 AAAGTTCTTGGATCTTTTTCATCGAAGTTGGCAACATACACTAGGAATTTCCTGAAGCGACGTTT AAAGTTCTTGGATCTTTTTCATCGAAGTTGGCGACATACACTAGGAATTTCCTGAAGCGACGTTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:5785902..5786002 32194978 MeRIP-seq:(Medium) rs1164391848 Functional Loss SNV dbSNP153 33..33 33 - - - 95862 RMVar_ID_95862 Human_SNP_ID_420395781 m1A Human chr10 + 5813723 5813723 5813723 CGGGGTGGAGGTGCACGGAGCCGCGGGCGGGGACTGCTGGCCACCACCGTTCTGACTCCCGCCGT CGGGGTGGAGGTGCACGGAGCCGCGGGCGGGGCCTGCTGGCCACCACCGTTCTGACTCCCGCCGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5813675..5813947 26863196 MeRIP-seq:(Medium) rs1201299926 Functional Loss SNV dbSNP153 33..33 33 - - - 95863 RMVar_ID_95863 Human_SNP_ID_420395789 m1A Human chr10 - 5813747 5813747 5813747 TGGACCGAGCGAGCTCCCGCCCCGACGGCGGGAGTCAGAACGGTGGTGGCCAGCAGTCCCCGCCC TGGACCGAGCGAGCTCCCGCCCCGACGGCGGGGGTCAGAACGGTGGTGGCCAGCAGTCCCCGCCC T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:5813702..5813809 26863196 MeRIP-seq:(Medium) rs1433562640 Functional Loss SNV dbSNP153 33..33 33 - - - 95864 RMVar_ID_95864 Human_SNP_ID_420416506 m1A Human chr10 + 5889744 5889744 5889744 GCGGCCCGTACGTGATTCGGGACTGAACACGTAAGGGAGTGGGGCGCGCCGCTACACCGCAAAGC GCGGCCCGTACGTGATTCGGGACTGAACACGTCAGGGAGTGGGGCGCGCCGCTACACCGCAAAGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:5889694..5889807 32194978 MeRIP-seq:(Medium) rs1262465841 Functional Loss SNV dbSNP153 33..33 33 - - - 95865 RMVar_ID_95865 Human_SNP_ID_420416774 m1A Human chr10 + 5890287 5890287 5890287 GGAGGAGCTCGCTGCCGGGGGACGCTGGGCTGAGCGGCCGGCGGCGCGGGCCCGGCGGCGGCGGC GGAGGAGCTCGCTGCCGGGGGACGCTGGGCTGGGCGGCCGGCGGCGCGGGCCCGGCGGCGGCGGC A G FBH1 Ensembl:ENSG00000134452 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:5890236..5890626;chr10:5890226..5890721;chr10:5890232..5891074 26863196 MeRIP-seq:(Medium) rs1214564741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135754,Human_RBP_ID_18416075,Human_RBP_ID_22886598,Human_RBP_ID_23117799,Human_RBP_ID_23123712 Human_Splice_Rec_1108915,Human_Splice_Rec_1108957,Human_Splice_Rec_1108997,Human_Splice_Rec_1109005 RMVar_hsa_circ_104599,RMVar_hsa_circ_141800 95866 RMVar_ID_95866 Human_SNP_ID_420416809 m1A Human chr10 - 5890348 5890348 5890348 CCACACTCCCTGCCACGTCTGCGGCCTCACGCACTGTGGCGCTCCGGACCCGGACCCCGCTGCCG CCACACTCCCTGCCACGTCTGCGGCCTCACGCCCTGTGGCGCTCCGGACCCGGACCCCGCTGCCG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr10:5890251..5890384;chr10:5890302..5891074 26863410,32194978 MeRIP-seq:(Medium) rs964675037 Functional Loss SNV dbSNP153 33..33 33 - - - 95867 RMVar_ID_95867 Human_SNP_ID_420418436 m1A Human chr10 + 5896320 5896320 5896320 GTGAAGAGATTTGAGGGGTGGTGGAGGGCTAAACTCCAGATCTGACCACTTCAAAGTCAGCAAAG GTGAAGAGATTTGAGGGGTGGTGGAGGGCTAAGCTCCAGATCTGACCACTTCAAAGTCAGCAAAG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:5896318..5896463 26863196 MeRIP-seq:(Medium) rs1021782390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8989768,Human_RBP_ID_9413055 RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 95868 RMVar_ID_95868 Human_SNP_ID_420420159 m1A Human chr10 - 5902952 5902951 5902952 TCATTAGTTATCACCGATTCTACAAGCTAGCCAGCACATTATACTCAAGTTTCTGCATAGTGACA TCATTAGTTATCACCGATTCTACAAGCTAGCC_GCACATTATACTCAAGTTTCTGCATAGTGACA CT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:5902946..5903057 26863410 MeRIP-seq:(Medium) rs908789627 Functional Loss DEL dbSNP153 33..33 33 - - - 95869 RMVar_ID_95869 Human_SNP_ID_420420161 m1A Human chr10 - 5902956 5902956 5902956 ATATTCATTAGTTATCACCGATTCTACAAGCTAGCCAGCACATTATACTCAAGTTTCTGCATAGT ATATTCATTAGTTATCACCGATTCTACAAGCTCGCCAGCACATTATACTCAAGTTTCTGCATAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:5902953..5903124 26863196 MeRIP-seq:(Medium) rs940258576 Functional Loss SNV dbSNP153 33..33 33 - - - 95870 RMVar_ID_95870 Human_SNP_ID_420421023 m1A Human chr10 - 5906007 5906007 5906007 GACCTGTAGAGAGAACCCAAACAGGATGGACAAGAAATGAACGATGACTGTTGACCTGCTGTTAA GACCTGTAGAGAGAACCCAAACAGGATGGACATGAAATGAACGATGACTGTTGACCTGCTGTTAA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:5906004..5906099 26863196 MeRIP-seq:(Medium) rs1181208195 Functional Loss SNV dbSNP153 33..33 33 - - - 95871 RMVar_ID_95871 Human_SNP_ID_420424007 m1A Human chr10 + 5916635 5916635 5916635 AAACGGGAAGTGTTAGGGATCTGAGGATGGGGAAATGGGAAGTGTTAGGGGTCTGAGGATGGGGG AAACGGGAAGTGTTAGGGATCTGAGGATGGGGGAATGGGAAGTGTTAGGGGTCTGAGGATGGGGG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:5916510..5916650 26863196 MeRIP-seq:(Medium) rs1384322023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5340339,Human_RBP_ID_8172103 RMVar_hsa_circ_348344,RMVar_hsa_circ_59483,RMVar_hsa_circ_4909,RMVar_hsa_circ_292928,RMVar_hsa_circ_321002,RMVar_hsa_circ_64634,RMVar_hsa_circ_341514,RMVar_hsa_circ_141801,RMVar_hsa_circ_368514,RMVar_hsa_circ_51284,RMVar_hsa_circ_27380,RMVar_hsa_circ_141806,RMVar_hsa_circ_53112,RMVar_hsa_circ_71881,RMVar_hsa_circ_141809,RMVar_hsa_circ_327118 95872 RMVar_ID_95872 Human_SNP_ID_420431141 m1A Human chr10 + 5943719 5943719 5943719 GCTGGTGGCAGGGGCTCGGCTCAGCTGCTCCCAGGCATTCCTTCCTCCCCTGCTCATGTTCGGTG GCTGGTGGCAGGGGCTCGGCTCAGCTGCTCCCCGGCATTCCTTCCTCCCCTGCTCATGTTCGGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5943566..5943814 26863196 MeRIP-seq:(Medium) rs1004824267 Functional Loss SNV dbSNP153 33..33 33 - - - 95873 RMVar_ID_95873 Human_SNP_ID_420431732 m1A Human chr10 - 5945767 5945767 5945767 GCTGCTCAGTAACTGGAAGGAAAATGAAACTGAAAAAGAGCAAGGGTCCCGTAGGATTGAACACA GCTGCTCAGTAACTGGAAGGAAAATGAAACTGGAAAAGAGCAAGGGTCCCGTAGGATTGAACACA T C IL15RA,AL137186.2 Ensembl:ENSG00000134470,Ensembl:ENSG00000232807 Protein coding,lincRNA intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5945701..5945899 26863196 MeRIP-seq:(Medium) rs1474674537 Functional Loss SNV dbSNP153 33..33 33 - - - 95874 RMVar_ID_95874 Human_SNP_ID_420440016 m1A Human chr10 - 5977353 5977353 5977353 GGCGCCCGGGCGGGACTTGGAAGGGGGCCGGGACGTGGAGCTGGAGGGAACCGGGCGCCCCATCT GGCGCCCGGGCGGGACTTGGAAGGGGGCCGGGGCGTGGAGCTGGAGGGAACCGGGCGCCCCATCT T C IL15RA Ensembl:ENSG00000134470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:5977060..5977531 26863196 MeRIP-seq:(Medium) rs945426933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9320805 95875 RMVar_ID_95875 Human_SNP_ID_420469031 m1A Human chr10 - 6089077 6089077 6089077 CAGGAGGCCTCGGCGGCGCCCACCCTTCGCTGAGTCCTCAGGGCGCTCGGCGGCGCGGGGTCAGG CAGGAGGCCTCGGCGGCGCCCACCCTTCGCTGGGTCCTCAGGGCGCTCGGCGGCGCGGGGTCAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:6089026..6089201 26863196 MeRIP-seq:(Medium) rs1340017948 Functional Loss SNV dbSNP153 33..33 33 - - - 95876 RMVar_ID_95876 Human_SNP_ID_420469319 m1A Human chr10 - 6089895 6089895 6089895 CCTTCCAGACCCCACTTGCGTTTCTCAAATCAACCCGGGCCTGGGTTTTCACGCCTGCTTTCCCA CCTTCCAGACCCCACTTGCGTTTCTCAAATCACCCCGGGCCTGGGTTTTCACGCCTGCTTTCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:6089889..6090141 26863196 MeRIP-seq:(Medium) rs923413986 Functional Loss SNV dbSNP153 33..33 33 - - - 95877 RMVar_ID_95877 Human_SNP_ID_420469328 m1A Human chr10 + 6089938 6089929 6089939 AACGCAAGTGGGGTCTGGAAGGACCTCTCTTGAGAGAGGAGGTCATGCTTATGTTGAGTCTTGAA AACGCAAGTGGGGTCTGGAAGGAC__________AGAGGAGGTCATGCTTATGTTGAGTCTTGAA CCTCTCTTGAG C RBM17 Ensembl:ENSG00000134453 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:6089935..6090124 26863196 MeRIP-seq:(Medium) rs1341971458 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_8336021 Human_Splice_Rec_1109439 95878 RMVar_ID_95878 Human_SNP_ID_420473562 m1A Human chr10 + 6106087 6106087 6106087 TCTTCTGGTCAAGAGGAAGTCATCCCAGGTTCAGGTCTCTAAATTGGTTCATCTGTGATGAACAT TCTTCTGGTCAAGAGGAAGTCATCCCAGGTTCCGGTCTCTAAATTGGTTCATCTGTGATGAACAT A C RBM17 Ensembl:ENSG00000134453 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:6106085..6106227 26863196 MeRIP-seq:(Medium) rs528949315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48376,RMVar_hsa_circ_358402,RMVar_hsa_circ_351198,RMVar_hsa_circ_71768,RMVar_hsa_circ_62455,RMVar_hsa_circ_297148,RMVar_hsa_circ_368877,RMVar_hsa_circ_141816,RMVar_hsa_circ_363856 95879 RMVar_ID_95879 Human_SNP_ID_420477999 m1A Human chr10 - 6121537 6121530 6121537 AAGTTTAGCTTTCCCATGCCCCCACCCCCCGCACCGTTGCCCGCCGCCCCCCCCCCCCCCCCCCG AAGTTTAGCTTTCCCATGCCCCCACCCCCCGC_______CCCGCCGCCCCCCCCCCCCCCCCCCG GCAACGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr10:6121501..6121550 26863196 MeRIP-seq:(Medium) rs1425190743 Functional Loss DEL dbSNP153 33..39 33 - - - 95880 RMVar_ID_95880 Human_SNP_ID_420478009 m1A Human chr10 - 6121537 6121537 6121537 AAGTTTAGCTTTCCCATGCCCCCACCCCCCGCACCGTTGCCCGCCGCCCCCCCCCCCCCCCCCCG AAGTTTAGCTTTCCCATGCCCCCACCCCCCGCCCCGTTGCCCGCCGCCCCCCCCCCCCCCCCCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr10:6121501..6121550 26863196 MeRIP-seq:(Medium) rs1016388706 Functional Loss SNV dbSNP153 33..33 33 - - - 95881 RMVar_ID_95881 Human_SNP_ID_420484130 m1A Human chr10 - 6144962 6144962 6144962 GCCGGGGGCGCTCCCCGCGGGGCCGGCCCGCGACACCCAGACAGGACGACGTCCAAGCGGCAGCC GCCGGGGGCGCTCCCCGCGGGGCCGGCCCGCGGCACCCAGACAGGACGACGTCCAAGCGGCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:6144926..6145015 26863196 MeRIP-seq:(Medium) rs1283636389 Functional Loss SNV dbSNP153 33..33 33 - - - 95882 RMVar_ID_95882 Human_SNP_ID_420484222 m1A Human chr10 - 6145191 6145191 6145191 CGGATCTGGAGGGACACGCGGGTCCGGGGCGCAGCGCAGGGCGGAGGGGACAAGGCGGAGCGCGT CGGATCTGGAGGGACACGCGGGTCCGGGGCGCCGCGCAGGGCGGAGGGGACAAGGCGGAGCGCGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:6145182..6145337 26863196 MeRIP-seq:(Medium) rs1376533175 Functional Loss SNV dbSNP153 33..33 33 - - - 95883 RMVar_ID_95883 Human_SNP_ID_420484616 m1A Human chr10 + 6146373 6146373 6146373 GGTGGCTGCTGACTCTCCTGTCCCGTTGGGGTAGAGAGATGGGGGAGGGTGGCCAGAAGGAAGGT GGTGGCTGCTGACTCTCCTGTCCCGTTGGGGTGGAGAGATGGGGGAGGGTGGCCAGAAGGAAGGT A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:6146365..6146501 32194978 MeRIP-seq:(Medium) rs752840290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5234539,Human_RBP_ID_9320470,Human_RBP_ID_18475927 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 95884 RMVar_ID_95884 Human_SNP_ID_420492941 m1A Human chr10 + 6176128 6176128 6176128 GTGGTGTTCGTGCAGTGGAATACTACAGAAGGATGAAGAAGAACCAGCTATTGCAGGAAGGGACA GTGGTGTTCGTGCAGTGGAATACTACAGAAGGGTGAAGAAGAACCAGCTATTGCAGGAAGGGACA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:6176117..6176286 26863196 MeRIP-seq:(Medium) rs1337828952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 95885 RMVar_ID_95885 Human_SNP_ID_420501169 m1A Human chr10 + 6202959 6202959 6202959 ATCCCAGCCAAGCCGGAGAGGAGGCGAGCAGCAGGGCCTGGTGGCGAGAGCGCGGCTGTCACTGC ATCCCAGCCAAGCCGGAGAGGAGGCGAGCAGCGGGGCCTGGTGGCGAGAGCGCGGCTGTCACTGC A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:6202953..6203193 26863196 MeRIP-seq:(Medium) rs1311619225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416214 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 95886 RMVar_ID_95886 Human_SNP_ID_420501187 m1A Human chr10 + 6202975 6202975 6202975 AGAGGAGGCGAGCAGCAGGGCCTGGTGGCGAGAGCGCGGCTGTCACTGCGCCCGAGCATCCCAGA AGAGGAGGCGAGCAGCAGGGCCTGGTGGCGAGGGCGCGGCTGTCACTGCGCCCGAGCATCCCAGA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:6202964..6203106 26863196 MeRIP-seq:(Medium) rs1327058673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416214 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 95887 RMVar_ID_95887 Human_SNP_ID_420509284 m1A Human chr10 + 6226257 6226257 6226257 CGCAATAGTGTCACCCCGCTAGCCAGCCCCGAACCCACCAAAAAGCCTCGCATCAACAGCTTTGA CGCAATAGTGTCACCCCGCTAGCCAGCCCCGAGCCCACCAAAAAGCCTCGCATCAACAGCTTTGA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:6226212..6226328 26863196 MeRIP-seq:(Medium) rs757173698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1109526,Human_Splice_Rec_1109554,Human_Splice_Rec_1109592,Human_Splice_Rec_1109622,Human_Splice_Rec_1109652,Human_Splice_Rec_1109686,Human_Splice_Rec_1109718,Human_Splice_Rec_1109746,Human_Splice_Rec_1109804,Human_Splice_Rec_1109834,Human_Splice_Rec_1109864,Human_Splice_Rec_1109892,Human_Splice_Rec_1109908,Human_Splice_Rec_1109912,Human_Splice_Rec_1109916 RMVar_hsa_circ_15369,RMVar_hsa_circ_49982 95888 RMVar_ID_95888 Human_SNP_ID_420777337 m1A Human chr10 - 7235603 7235598 7235603 TATGTGGGGTGTGTGTGTGTATCTAATATGTGATGTGTATGTGTGGTACGTCTGTGTGGTATGTG TATGTGGGGTGTGTGTGTGTATCTAATATGTG_____TATGTGTGGTACGTCTGTGTGGTATGTG ACACAT A SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:7235482..7235639 26863196 MeRIP-seq:(Medium) rs1182595289 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_23466594 RMVar_hsa_circ_15750,RMVar_hsa_circ_124701,RMVar_hsa_circ_141825,RMVar_hsa_circ_141827,RMVar_hsa_circ_88146,RMVar_hsa_circ_266261,RMVar_hsa_circ_289495,RMVar_hsa_circ_317668,RMVar_hsa_circ_366882,RMVar_hsa_circ_319799,RMVar_hsa_circ_58187,RMVar_hsa_circ_141832,RMVar_hsa_circ_141833,RMVar_hsa_circ_141831,RMVar_hsa_circ_304650,RMVar_hsa_circ_83092,RMVar_hsa_circ_141834,RMVar_hsa_circ_141835,RMVar_hsa_circ_114527,RMVar_hsa_circ_13099,RMVar_hsa_circ_141844,RMVar_hsa_circ_126640,RMVar_hsa_circ_311597,RMVar_hsa_circ_141841,RMVar_hsa_circ_361628,RMVar_hsa_circ_376735,RMVar_hsa_circ_317925,RMVar_hsa_circ_282379,RMVar_hsa_circ_294917,RMVar_hsa_circ_141846,RMVar_hsa_circ_141848,RMVar_hsa_circ_141847,RMVar_hsa_circ_141845,RMVar_hsa_circ_141842,RMVar_hsa_circ_141843,RMVar_hsa_circ_267184,RMVar_hsa_circ_328246,RMVar_hsa_circ_351122,RMVar_hsa_circ_310551,RMVar_hsa_circ_141851 95889 RMVar_ID_95889 Human_SNP_ID_420822724 m1A Human chr10 - 7410981 7410981 7410981 GGAGCCGGAGGACCGGAGCGGGCGCGCGAGGGAGGCGGCGGGCGGGGAGCGAGCGGGCAAGGGCG GGAGCCGGAGGACCGGAGCGGGCGCGCGAGGGTGGCGGCGGGCGGGGAGCGAGCGGGCAAGGGCG T A SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:7410845..7411014 26863196 MeRIP-seq:(Medium) rs1052674541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748620,Human_RBP_ID_9340603,Human_RBP_ID_9413279,Human_RBP_ID_17345577,Human_RBP_ID_18416418,Human_RBP_ID_26316068,Human_RBP_ID_27835978 95890 RMVar_ID_95890 Human_SNP_ID_420923498 m1A Human chr10 - 7778940 7778940 7778940 ATAGACAGGGACCCAGAAACTATCCGCCGGCAACTGGAACTGGAGAAAAAGAAAAAGCAGGACCT ATAGACAGGGACCCAGAAACTATCCGCCGGCAGCTGGAACTGGAGAAAAAGAAAAAGCAGGACCT T C KIN Ensembl:ENSG00000151657 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:7778891..7778956 26863196 MeRIP-seq:(Medium) rs766056160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4128687,Human_RBP_ID_18432045,Human_RBP_ID_22788815,Human_RBP_ID_26316070 Human_Splice_Rec_1110790 RMVar_hsa_circ_11989,RMVar_hsa_circ_71746,RMVar_hsa_circ_64818,RMVar_hsa_circ_73036,RMVar_hsa_circ_73806,RMVar_hsa_circ_141897,RMVar_hsa_circ_302773,RMVar_hsa_circ_318837,RMVar_hsa_circ_141898,RMVar_hsa_circ_288312 95891 RMVar_ID_95891 Human_SNP_ID_420925929 m1A Human chr10 - 7788251 7788251 7788251 CTTCCCGCAAGCTGCCATACCATTGCGGCTGCAAGGTCCAGGCCGACAGCCCAGCGACACCCGCG CTTCCCGCAAGCTGCCATACCATTGCGGCTGCGAGGTCCAGGCCGACAGCCCAGCGACACCCGCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:7788201..7788275 32194978 MeRIP-seq:(Medium) rs1257360560 Functional Loss SNV dbSNP153 33..33 33 - - - 95892 RMVar_ID_95892 Human_SNP_ID_420927577 m1A Human chr10 - 7796103 7796103 7796103 TTTCGAACTTGAATCCTGAGGATAAAAGTTTTAAAAATGTTTCAGTTTTTTGAAAAATAGTTCCA TTTCGAACTTGAATCCTGAGGATAAAAGTTTTGAAAATGTTTCAGTTTTTTGAAAAATAGTTCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:7796101..7796175 32194978 MeRIP-seq:(Medium) rs757777839 Functional Loss SNV dbSNP153 33..33 33 - - - 95893 RMVar_ID_95893 Human_SNP_ID_420928474 m1A Human chr10 - 7799192 7799192 7799192 ATGAAAATAAACAATATATATTTAAATTACCTATAAAGTATGCCTCTGATTTTGTCACCAATTCC ATGAAAATAAACAATATATATTTAAATTACCTGTAAAGTATGCCTCTGATTTTGTCACCAATTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:7799151..7799251 32194978 MeRIP-seq:(Medium) rs1273428741 Functional Loss SNV dbSNP153 33..33 33 - - - 95894 RMVar_ID_95894 Human_SNP_ID_420937170 m1A Human chr10 - 7833957 7833957 7833957 TGTTGTCCTGTGCCGGAGGACAGCAGGCAGCCATGGTGCCCAGCGGGAATGGCAAGATCTTGAAG TGTTGTCCTGTGCCGGAGGACAGCAGGCAGCCGTGGTGCCCAGCGGGAATGGCAAGATCTTGAAG T C AL353754.1 Ensembl:ENSG00000233990 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:7833921..7834035 32194978 MeRIP-seq:(Medium) rs1273154766 Functional Loss SNV dbSNP153 33..33 33 - - - 95895 RMVar_ID_95895 Human_SNP_ID_420941753 m1A Human chr10 + 7851224 7851224 7851224 AGTCAGGGGAACTAGTGAGAAAGCAACATTCTAGCAAAGACTTCAAAGAGGGGAGAGGGATAGCC AGTCAGGGGAACTAGTGAGAAAGCAACATTCTCGCAAAGACTTCAAAGAGGGGAGAGGGATAGCC A C TAF3 Ensembl:ENSG00000165632 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:7851213..7851365 26863196 MeRIP-seq:(Medium) rs1046830234 Functional Loss SNV dbSNP153 33..33 33 - - - 95896 RMVar_ID_95896 Human_SNP_ID_420969872 m1A Human chr10 + 7965618 7965618 7965618 GAAAGAGAAGGTGAAGGAGAAAGAAAAGAAAAAGGACAAAAAGGAGAAGAAGAAAAAGAAGGAAA GAAAGAGAAGGTGAAGGAGAAAGAAAAGAAAAGGGACAAAAAGGAGAAGAAGAAAAAGAAGGAAA A G TAF3 Ensembl:ENSG00000165632 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:7965073..8009262;chr10:7965077..8009117 26863196 MeRIP-seq:(Medium) rs1366568366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24541933 RMVar_hsa_circ_266081,RMVar_hsa_circ_360576 95897 RMVar_ID_95897 Human_SNP_ID_420980578 m1A Human chr10 + 8009147 8009147 8009147 CCGGCGCCCTCGCAGAACAGGCCGAAGACCCCACCGCCGGCCCCCGCGCCCGCCCCCGGCCCCAT CCGGCGCCCTCGCAGAACAGGCCGAAGACCCCCCCGCCGGCCCCCGCGCCCGCCCCCGGCCCCAT A C TAF3 Ensembl:ENSG00000165632 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:8009120..8009246 26863196 MeRIP-seq:(Medium) rs191001876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1110938 RMVar_hsa_circ_121566,RMVar_hsa_circ_266081,RMVar_hsa_circ_141912 95898 RMVar_ID_95898 Human_SNP_ID_420994976 m1A Human chr10 - 8055540 8055540 8055540 GCTCCTGCCGTCGGAGGGTCGGGGGTCGTTGAATGATTTGCTTTCGGTGGGGGGATGGGAAGGCT GCTCCTGCCGTCGGAGGGTCGGGGGTCGTTGACTGATTTGCTTTCGGTGGGGGGATGGGAAGGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:8055491..8055706 26863196 MeRIP-seq:(Medium) rs76250826 Functional Loss SNV dbSNP153 33..33 33 - - - 95899 RMVar_ID_95899 Human_SNP_ID_421886056 m1A Human chr10 + 11457593 11457593 11457593 CATGCCTACCCCACATACACATCACAGTGGCAAATTTCCTCACACATCCCATGCAGCTGCTCTTG CATGCCTACCCCACATACACATCACAGTGGCACATTTCCTCACACATCCCATGCAGCTGCTCTTG A C lnc-CELF2-2 RNACentral:URS0000E97799 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11457546..11457611 26863196 MeRIP-seq:(Medium) rs892323387 Functional Loss SNV dbSNP153 33..33 33 - - - 95900 RMVar_ID_95900 Human_SNP_ID_421886057 m1A Human chr10 + 11457593 11457593 11457593 CATGCCTACCCCACATACACATCACAGTGGCAAATTTCCTCACACATCCCATGCAGCTGCTCTTG CATGCCTACCCCACATACACATCACAGTGGCAGATTTCCTCACACATCCCATGCAGCTGCTCTTG A G lnc-CELF2-2 RNACentral:URS0000E97799 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11457546..11457611 26863196 MeRIP-seq:(Medium) rs892323387 Functional Loss SNV dbSNP153 33..33 33 - - - 95901 RMVar_ID_95901 Human_SNP_ID_421887998 m1A Human chr10 - 11463635 11463635 11463635 AGGACCGGGACGCCCGAGAGAGCACAGCCGCCAAGACGGAAATCGGTGGAGGAGGAGAGCAAAAA AGGACCGGGACGCCCGAGAGAGCACAGCCGCCGAGACGGAAATCGGTGGAGGAGGAGAGCAAAAA T C USP6NL Ensembl:ENSG00000148429 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11463533..11463773 26863196 MeRIP-seq:(Medium) rs112125973 Functional Loss SNV dbSNP153 33..33 33 - - - 95902 RMVar_ID_95902 Human_SNP_ID_421920767 m1A Human chr10 + 11597713 11597713 11597713 AATCTGCTGTCCAAGGTTTCTCAGAGGAATACATGTCCTAGTCAGGAAACAAAGAGAAAGAAATA AATCTGCTGTCCAAGGTTTCTCAGAGGAATACGTGTCCTAGTCAGGAAACAAAGAGAAAGAAATA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11597685..11597759 26863196 MeRIP-seq:(Medium) rs986142068 Functional Loss SNV dbSNP153 33..33 33 - - - 95903 RMVar_ID_95903 Human_SNP_ID_421924008 m1A Human chr10 - 11611512 11611512 11611512 GCCGCCGCCGCCGCCGCGCCGCGCCGCGCCGGATCTGCTCGGCCGCCCGGGACCGCCAGCTCTGT GCCGCCGCCGCCGCCGCGCCGCGCCGCGCCGGTTCTGCTCGGCCGCCCGGGACCGCCAGCTCTGT T A USP6NL Ensembl:ENSG00000148429 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:11611466..11611573 26863196 MeRIP-seq:(Medium) rs1274699889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_370697,Human_RBP_ID_4136154,Human_RBP_ID_18416080,Human_RBP_ID_22886599 Human_Splice_Rec_1112237,Human_Splice_Rec_1112321 RMVar_hsa_circ_104913,RMVar_hsa_circ_142034,RMVar_hsa_circ_87518,RMVar_hsa_circ_142039 95904 RMVar_ID_95904 Human_SNP_ID_421924038 m1A Human chr10 - 11611545 11611545 11611545 AAGGGAAACAATGGGGCGGAGGGCACTGCGGTAGCCGCCGCCGCCGCCGCGCCGCGCCGCGCCGG AAGGGAAACAATGGGGCGGAGGGCACTGCGGTGGCCGCCGCCGCCGCCGCGCCGCGCCGCGCCGG T C USP6NL Ensembl:ENSG00000148429 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:11611471..11611596 26863196 MeRIP-seq:(Medium) rs910678608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_370697,Human_RBP_ID_4136154,Human_RBP_ID_18416080,Human_RBP_ID_22886599 RMVar_hsa_circ_104913,RMVar_hsa_circ_142034,RMVar_hsa_circ_87518,RMVar_hsa_circ_142039 95905 RMVar_ID_95905 Human_SNP_ID_421958648 m1A Human chr10 - 11742469 11742459 11742469 GCTGTGAGCAGGGCCGGGACGGAACTCGACGGAACTCGACGGTGGCCGAGACCCGGACGGAACCG GCTGTGAGCAGGGCCGGGACGGAACTCGACGG__________TGGCCGAGACCCGGACGGAACCG ACCGTCGAGTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11742420..11742495 26863196 MeRIP-seq:(Medium) rs961343355 Functional Loss DEL dbSNP153 33..42 33 - - - 95906 RMVar_ID_95906 Human_SNP_ID_421979652 m1A Human chr10 - 11823416 11823416 11823416 GGACTCAGGTGTCCACGCCGCCAGCGACCCGGAGCCCTCACGCCGCCGCCCGTCTGGCGCAGACT GGACTCAGGTGTCCACGCCGCCAGCGACCCGGGGCCCTCACGCCGCCGCCCGTCTGGCGCAGACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:11823318..11823642 26863196 MeRIP-seq:(Medium) rs1336723164 Functional Loss SNV dbSNP153 33..33 33 - - - 95907 RMVar_ID_95907 Human_SNP_ID_421993260 m1A Human chr10 - 11869812 11869785 11869813 TTGGGCTGCGCCGGGTGGCTGGGCCCCGGGCCAGGGTCTCCACTGCGGGGCCCCCGGGCGGCAGG TTGGGCTGCGCCGGGTGGCTGGGCCCCGGGC____________________________GGCAGG CGCCCGGGGGCCCCGCAGTGGAGACCCTG C PROSER2-AS1 Ensembl:ENSG00000225778 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:11866700..11870293 26863196 MeRIP-seq:(Medium) rs1370801563 Functional Loss DEL dbSNP153 32..59 33 - - - RMVar_hsa_circ_87886,RMVar_hsa_circ_93650,RMVar_hsa_circ_142046,RMVar_hsa_circ_142047 95908 RMVar_ID_95908 Human_SNP_ID_421993277 m1A Human chr10 - 11869803 11869803 11869803 GCCGGGTGGCTGGGCCCCGGGCCAGGGTCTCCACTGCGGGGCCCCCGGGCGGCAGGTGTCCTCCA GCCGGGTGGCTGGGCCCCGGGCCAGGGTCTCCGCTGCGGGGCCCCCGGGCGGCAGGTGTCCTCCA T C PROSER2-AS1 Ensembl:ENSG00000225778 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:11869752..11869852 32194978 MeRIP-seq:(Medium) rs755745570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87886,RMVar_hsa_circ_93650,RMVar_hsa_circ_142046,RMVar_hsa_circ_142047 95909 RMVar_ID_95909 Human_SNP_ID_421993281 m1A Human chr10 - 11869812 11869812 11869812 TTGGGCTGCGCCGGGTGGCTGGGCCCCGGGCCAGGGTCTCCACTGCGGGGCCCCCGGGCGGCAGG TTGGGCTGCGCCGGGTGGCTGGGCCCCGGGCCGGGGTCTCCACTGCGGGGCCCCCGGGCGGCAGG T C PROSER2-AS1 Ensembl:ENSG00000225778 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:11866700..11870293 26863196 MeRIP-seq:(Medium) rs753405251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87886,RMVar_hsa_circ_93650,RMVar_hsa_circ_142046,RMVar_hsa_circ_142047 95910 RMVar_ID_95910 Human_SNP_ID_421993344 m1A Human chr10 + 11869895 11869895 11869895 CAACATCATCGTCACCAACGGCGCGGCCCGGGAGCCCCGCAGGACCCTGTCCAGGGCGGCCGTCA CAACATCATCGTCACCAACGGCGCGGCCCGGGGGCCCCGCAGGACCCTGTCCAGGGCGGCCGTCA A G PROSER2 Ensembl:ENSG00000148426 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11866749..11870051 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18970613,Human_RBP_ID_27404165 RMVar_hsa_circ_113879,RMVar_hsa_circ_85855,RMVar_hsa_circ_142043,RMVar_hsa_circ_142045 95911 RMVar_ID_95911 Human_SNP_ID_421993457 m1A Human chr10 + 11870080 11870080 11870080 CGCGTGGCCGGGGCCTGCCGGGCCCCGCTGAGAGTCTCCGGGCAGGGGGTCAGGCTCCGCGGGGC CGCGTGGCCGGGGCCTGCCGGGCCCCGCTGAGTGTCTCCGGGCAGGGGGTCAGGCTCCGCGGGGC A T PROSER2 Ensembl:ENSG00000148426 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:11870000..11870100 26863410 MeRIP-seq:(Medium) rs1278497164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113879,RMVar_hsa_circ_85855,RMVar_hsa_circ_142043,RMVar_hsa_circ_142045 95912 RMVar_ID_95912 Human_SNP_ID_421993664 m1A Human chr10 - 11870381 11870381 11870381 GCGGCCCTCACGAACTCTCCCTGAGCAGCCCCAGCTTCCGCAGGGCCTCCCTGCGCGCCTCCTCC GCGGCCCTCACGAACTCTCCCTGAGCAGCCCCTGCTTCCGCAGGGCCTCCCTGCGCGCCTCCTCC T A PROSER2-AS1 Ensembl:ENSG00000225778 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:11870332..11870476 26863196 MeRIP-seq:(Medium) rs914518606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87886,RMVar_hsa_circ_93650,RMVar_hsa_circ_142046,RMVar_hsa_circ_142047 95913 RMVar_ID_95913 Human_SNP_ID_422038410 m1A Human chr10 - 12035199 12035199 12035199 AGAAAAAAGGAAGACAAGGAACGCAAGAAAAAAGACGAAGAAAAGGTGAAGGCAGAGGAAGAATC AGAAAAAAGGAAGACAAGGAACGCAAGAAAAAGGACGAAGAAAAGGTGAAGGCAGAGGAAGAATC T C UPF2 Ensembl:ENSG00000151461 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:12029458..12035450 26863196 MeRIP-seq:(Medium) rs1366590122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27764,Human_RBP_ID_192338,Human_RBP_ID_1452947,Human_RBP_ID_5545174,Human_RBP_ID_5935294,Human_RBP_ID_18970615,Human_RBP_ID_22030211,Human_RBP_ID_24541945 RMVar_hsa_circ_95739,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_142082,RMVar_hsa_circ_347609 95914 RMVar_ID_95914 Human_SNP_ID_422038460 m1A Human chr10 - 12035318 12035318 12035318 GCAGTGAAAGGCGGACAGTGAGCAGCAAGGAGAGGCCAAAAGACGATATCAAGCTCACTGCCAAG GCAGTGAAAGGCGGACAGTGAGCAGCAAGGAGTGGCCAAAAGACGATATCAAGCTCACTGCCAAG T A UPF2 Ensembl:ENSG00000151461 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:12035122..12035448 26863196 MeRIP-seq:(Medium) rs1169745466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27764,Human_RBP_ID_192339,Human_RBP_ID_862164,Human_RBP_ID_5520045,Human_RBP_ID_5545176,Human_RBP_ID_18587927,Human_RBP_ID_24541947,Human_RBP_ID_24785947,Human_RBP_ID_26316098 RMVar_hsa_circ_95739,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_347609 95915 RMVar_ID_95915 Human_SNP_ID_422040455 m1A Human chr10 - 12042787 12042787 12042787 GGGAGAGCCCGAGCGCTGGAGTTGGTGCTGGGAAACCCGGGGCTAATGTTGACAACAGGCTCGAG GGGAGAGCCCGAGCGCTGGAGTTGGTGCTGGGCAACCCGGGGCTAATGTTGACAACAGGCTCGAG T G UPF2 Ensembl:ENSG00000151461 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12042180..12042825 26863196 MeRIP-seq:(Medium) rs964993726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28898,Human_RBP_ID_371785,Human_RBP_ID_8765538,Human_RBP_ID_9273771,Human_RBP_ID_9320813,Human_RBP_ID_18416082,Human_RBP_ID_23438262,Human_RBP_ID_24541948,Human_RBP_ID_26316100,Human_RBP_ID_26767775,Human_RBP_ID_27801887 Human_Splice_Rec_1112437 95916 RMVar_ID_95916 Human_SNP_ID_422048619 m1A Human chr10 + 12069227 12069227 12069227 ATGGGGCCCGGGCGGTGGGAGCGGGGGCTGGGACGCAGAAGCCTCCCCTGGCCGATTTGCGGTGG ATGGGGCCCGGGCGGTGGGAGCGGGGGCTGGGTCGCAGAAGCCTCCCCTGGCCGATTTGCGGTGG A T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12069219..12069305 26863196 MeRIP-seq:(Medium) rs1284809942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5935877 RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 95917 RMVar_ID_95917 Human_SNP_ID_422050170 m1A Human chr10 - 12074762 12074762 12074762 CCAAAGTGCTGGGATGACAGGCATGAGCCACCAGGCCTGACCTGTTTATTTGTTTTTTTGAGACA CCAAAGTGCTGGGATGACAGGCATGAGCCACCGGGCCTGACCTGTTTATTTGTTTTTTTGAGACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12074759..12074869 26863196 MeRIP-seq:(Medium) rs1213842522 Functional Loss SNV dbSNP153 33..33 33 - - - 95918 RMVar_ID_95918 Human_SNP_ID_422051083 m1A Human chr10 + 12077747 12077747 12077747 TCAAGATTGGAGGGTGCGGGTGAGGGCCACTGAGTACCTTCACGTCGTACTCATGCTCTCTAGGG TCAAGATTGGAGGGTGCGGGTGAGGGCCACTGTGTACCTTCACGTCGTACTCATGCTCTCTAGGG A T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12077746..12077974 26863196 MeRIP-seq:(Medium) rs1468820371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225497,Human_RBP_ID_747843,Human_RBP_ID_11280395 RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 95919 RMVar_ID_95919 Human_SNP_ID_422066433 m1A Human chr10 + 12129713 12129713 12129713 GGCCGGTAGGATCGCGTCGGGAGCCGGTACCGAGGCCCGAGCCGCGGGAGTCGAGCGAAGGCAGC GGCCGGTAGGATCGCGTCGGGAGCCGGTACCGGGGCCCGAGCCGCGGGAGTCGAGCGAAGGCAGC A G SEC61A2 Ensembl:ENSG00000065665 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12129667..12129901 26863196 MeRIP-seq:(Medium) rs1001144010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5459020 Human_Splice_Rec_1112585,Human_Splice_Rec_1112597,Human_Splice_Rec_1112617,Human_Splice_Rec_1112629,Human_Splice_Rec_1112651,Human_Splice_Rec_1112675,Human_Splice_Rec_1112701,Human_Splice_Rec_1112723,Human_Splice_Rec_1112737,Human_Splice_Rec_1112757 95920 RMVar_ID_95920 Human_SNP_ID_422066451 m1A Human chr10 + 12129743 12129743 12129743 CGAGGCCCGAGCCGCGGGAGTCGAGCGAAGGCAGCGCCGAGGCCGCGGTTTCCCCCTGGGCCTCC CGAGGCCCGAGCCGCGGGAGTCGAGCGAAGGCGGCGCCGAGGCCGCGGTTTCCCCCTGGGCCTCC A G SEC61A2 Ensembl:ENSG00000065665 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12129697..12129788 26863196 MeRIP-seq:(Medium) rs758005366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1732,Human_RBP_ID_4110196 Human_Splice_Rec_1112585,Human_Splice_Rec_1112597,Human_Splice_Rec_1112617,Human_Splice_Rec_1112629,Human_Splice_Rec_1112651,Human_Splice_Rec_1112675,Human_Splice_Rec_1112701,Human_Splice_Rec_1112723,Human_Splice_Rec_1112737,Human_Splice_Rec_1112757 95921 RMVar_ID_95921 Human_SNP_ID_422066452 m1A Human chr10 + 12129743 12129743 12129743 CGAGGCCCGAGCCGCGGGAGTCGAGCGAAGGCAGCGCCGAGGCCGCGGTTTCCCCCTGGGCCTCC CGAGGCCCGAGCCGCGGGAGTCGAGCGAAGGCTGCGCCGAGGCCGCGGTTTCCCCCTGGGCCTCC A T SEC61A2 Ensembl:ENSG00000065665 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12129697..12129788 26863196 MeRIP-seq:(Medium) rs758005366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1732,Human_RBP_ID_4110196 Human_Splice_Rec_1112585,Human_Splice_Rec_1112597,Human_Splice_Rec_1112617,Human_Splice_Rec_1112629,Human_Splice_Rec_1112651,Human_Splice_Rec_1112675,Human_Splice_Rec_1112701,Human_Splice_Rec_1112723,Human_Splice_Rec_1112737,Human_Splice_Rec_1112757 95922 RMVar_ID_95922 Human_SNP_ID_422084138 m1A Human chr10 + 12196018 12196018 12196018 AGTTGTAAACTTCTTAAAATTCCTCTCTCGACACTTCGGTAATTCCTCTTTCGAGACTAAAGCTC AGTTGTAAACTTCTTAAAATTCCTCTCTCGACGCTTCGGTAATTCCTCTTTCGAGACTAAAGCTC A G CDC123 Ensembl:ENSG00000151465 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12195968..12196094 26863196 MeRIP-seq:(Medium) rs1036495337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1112915 RMVar_hsa_circ_101900,RMVar_hsa_circ_116386,RMVar_hsa_circ_142176,RMVar_hsa_circ_79795,RMVar_hsa_circ_142177,RMVar_hsa_circ_142175 95923 RMVar_ID_95923 Human_SNP_ID_422084144 m1A Human chr10 + 12196041 12196041 12196041 TCTCTCGACACTTCGGTAATTCCTCTTTCGAGACTAAAGCTCTTTTTGTATGCGTGTGTGTCAAG TCTCTCGACACTTCGGTAATTCCTCTTTCGAGGCTAAAGCTCTTTTTGTATGCGTGTGTGTCAAG A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:12195990..12196108 26863196 MeRIP-seq:(Medium) rs1160629842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101900,RMVar_hsa_circ_116386,RMVar_hsa_circ_142176,RMVar_hsa_circ_79795,RMVar_hsa_circ_142177,RMVar_hsa_circ_142175 95924 RMVar_ID_95924 Human_SNP_ID_422084236 m1A Human chr10 - 12196266 12196266 12196266 AAGAACGGGTACCACGCGGAGAACTGGCAGTGAAGCACATGCTCCTTCTTCATCCTCCAGCTGCC AAGAACGGGTACCACGCGGAGAACTGGCAGTGCAGCACATGCTCCTTCTTCATCCTCCAGCTGCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:12196201..12198775 32194978 MeRIP-seq:(Medium) rs1466844228 Functional Loss SNV dbSNP153 33..33 33 - - - 95925 RMVar_ID_95925 Human_SNP_ID_422087952 m1A Human chr10 + 12209982 12209982 12209982 TGTTTGTGTTTTTTTAGGGATGATCCACCAACACATTCTCAGCCAGACAGTGATGATGAAGCAGA TGTTTGTGTTTTTTTAGGGATGATCCACCAACGCATTCTCAGCCAGACAGTGATGATGAAGCAGA A G CDC123 Ensembl:ENSG00000151465 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:12209976..12237228 32194978 MeRIP-seq:(Medium) rs761242933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27767,Human_RBP_ID_747549,Human_RBP_ID_861103,Human_RBP_ID_4110286,Human_RBP_ID_8984243,Human_RBP_ID_17771508,Human_RBP_ID_18970619,Human_RBP_ID_22431981,Human_RBP_ID_22878485 Human_Splice_Rec_1112920,Human_Splice_Rec_1112921,Human_Splice_Rec_1112932,Human_Splice_Rec_1112933,Human_Splice_Rec_1112952,Human_Splice_Rec_1112953,Human_Splice_Rec_1112978,Human_Splice_Rec_1112979,Human_Splice_Rec_1113000,Human_Splice_Rec_1113001 Human_miRNA_ID_2331696,Human_miRNA_ID_2918793,Human_miRNA_ID_2964778 RMVar_hsa_circ_142179,RMVar_hsa_circ_34496,RMVar_hsa_circ_101900,RMVar_hsa_circ_116386,RMVar_hsa_circ_142176,RMVar_hsa_circ_79795,RMVar_hsa_circ_142177,RMVar_hsa_circ_142175,RMVar_hsa_circ_88214,RMVar_hsa_circ_323301,RMVar_hsa_circ_373316,RMVar_hsa_circ_97480,RMVar_hsa_circ_142180,RMVar_hsa_circ_290366,RMVar_hsa_circ_142178,RMVar_hsa_circ_305039,RMVar_hsa_circ_142181 95926 RMVar_ID_95926 Human_SNP_ID_422099306 m1A Human chr10 + 12249619 12249619 12249619 CCAGCTTTCCGTTGCACAAACAGTGAAGTGACAGTCCAGCCCAGCCCCTATTTGAGTTACCGGCT CCAGCTTTCCGTTGCACAAACAGTGAAGTGACTGTCCAGCCCAGCCCCTATTTGAGTTACCGGCT A T CDC123 Ensembl:ENSG00000151465 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs749789079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_372431,Human_RBP_ID_17787304,Human_RBP_ID_18588479,Human_RBP_ID_22489502 Human_Splice_Rec_1112948,Human_Splice_Rec_1112970,Human_Splice_Rec_1112971,Human_Splice_Rec_1112994,Human_Splice_Rec_1112995,Human_Splice_Rec_1113024,Human_Splice_Rec_1113025,Human_Splice_Rec_1113038 Human_miRNA_ID_1980673,Human_miRNA_ID_1982399,Human_miRNA_ID_2541841,Human_miRNA_ID_2543716,Human_miRNA_ID_2545565,Human_miRNA_ID_2547421,Human_miRNA_ID_2549285,Human_miRNA_ID_2551154,Human_miRNA_ID_2553844,Human_miRNA_ID_2556560,Human_miRNA_ID_2558442,Human_miRNA_ID_2588861 RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_142191,RMVar_hsa_circ_142193,RMVar_hsa_circ_142192,RMVar_hsa_circ_142194 95927 RMVar_ID_95927 Human_SNP_ID_422099533 m1A Human chr10 + 12250404 12250404 12250404 CCCCACCGCTCCGGGAGCTGCTCATCAGCCGCAACTTCCTGCCGACCCTGATGCGGGTGGGCCGA CCCCACCGCTCCGGGAGCTGCTCATCAGCCGCGACTTCCTGCCGACCCTGATGCGGGTGGGCCGA A G CDC123 Ensembl:ENSG00000151465 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:12250294..12250550 32194978 MeRIP-seq:(Medium) rs764531888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_372437,Human_RBP_ID_4110435,Human_RBP_ID_8327823,Human_RBP_ID_17648223,Human_RBP_ID_17771582,Human_RBP_ID_26801827 Human_Splice_Rec_1112972,Human_Splice_Rec_1112996,Human_Splice_Rec_1113026,Human_Splice_Rec_1113036 Human_miRNA_ID_1182886 RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_142193,RMVar_hsa_circ_142192,RMVar_hsa_circ_142194 95928 RMVar_ID_95928 Human_SNP_ID_422128785 m1A Human chr10 + 12349399 12349399 12349399 GCGCTCTTGGGAGGGGAGCGGGACATCCCCGAAGGCGGCGCGCTGGAGGCGGGGAGCGGCCGGGG GCGCTCTTGGGAGGGGAGCGGGACATCCCCGACGGCGGCGCGCTGGAGGCGGGGAGCGGCCGGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12349208..12349438 26863196 MeRIP-seq:(Medium) rs1296922110 Functional Loss SNV dbSNP153 33..33 33 - - - 95929 RMVar_ID_95929 Human_SNP_ID_422128786 m1A Human chr10 + 12349399 12349399 12349399 GCGCTCTTGGGAGGGGAGCGGGACATCCCCGAAGGCGGCGCGCTGGAGGCGGGGAGCGGCCGGGG GCGCTCTTGGGAGGGGAGCGGGACATCCCCGAGGGCGGCGCGCTGGAGGCGGGGAGCGGCCGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12349208..12349438 26863196 MeRIP-seq:(Medium) rs1296922110 Functional Loss SNV dbSNP153 33..33 33 - - - 95930 RMVar_ID_95930 Human_SNP_ID_422151814 m1A Human chr10 + 12431381 12431381 12431381 CAGCTCATGGCTTAGAAAGGAGCCGGGTGCACAGGTGGGTCTGGGTGAGCTGGAGGCTGTGATCA CAGCTCATGGCTTAGAAAGGAGCCGGGTGCACGGGTGGGTCTGGGTGAGCTGGAGGCTGTGATCA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12431377..12431467 26863196 MeRIP-seq:(Medium) rs1156630060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 95931 RMVar_ID_95931 Human_SNP_ID_422162573 m1A Human chr10 - 12473129 12473117 12473129 ACCTGTCTGTGCCTACAGCTTCTGCATCCACCATTGCTTCCACCTGGCGCACCCTCTCCCCTCCT ACCTGTCTGTGCCTACAGCTTCTGCATCCACC____________TGGCGCACCCTCTCCCCTCCT AGGTGGAAGCAAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12473113..12473185 26863196 MeRIP-seq:(Medium) rs1289557495 Functional Loss DEL dbSNP153 33..44 33 - - - 95932 RMVar_ID_95932 Human_SNP_ID_422162577 m1A Human chr10 - 12473129 12473129 12473129 ACCTGTCTGTGCCTACAGCTTCTGCATCCACCATTGCTTCCACCTGGCGCACCCTCTCCCCTCCT ACCTGTCTGTGCCTACAGCTTCTGCATCCACCGTTGCTTCCACCTGGCGCACCCTCTCCCCTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12473113..12473185 26863196 MeRIP-seq:(Medium) rs1394944150 Functional Loss SNV dbSNP153 33..33 33 - - - 95933 RMVar_ID_95933 Human_SNP_ID_422165718 m1A Human chr10 - 12485429 12485429 12485429 TGGGGCCACCTCGCCACTGAACCTGGGGCCCAAGCTTCACCACCATTGTGCTGCCTGTTTCTACT TGGGGCCACCTCGCCACTGAACCTGGGGCCCATGCTTCACCACCATTGTGCTGCCTGTTTCTACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12485426..12485541 26863196 MeRIP-seq:(Medium) rs1280948543 Functional Loss SNV dbSNP153 33..33 33 - - - 95934 RMVar_ID_95934 Human_SNP_ID_422182553 m1A Human chr10 - 12546202 12546202 12546202 TCCTTCCTGGTCCCGTAGCCCCCAGCGAGCCCACTGCTACCTGCTATCTCCTATCTGTTACTGAA TCCTTCCTGGTCCCGTAGCCCCCAGCGAGCCCGCTGCTACCTGCTATCTCCTATCTGTTACTGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12546198..12546309 26863196 MeRIP-seq:(Medium) rs1256435597 Functional Loss SNV dbSNP153 33..33 33 - - - 95935 RMVar_ID_95935 Human_SNP_ID_422201670 m1A Human chr10 - 12615981 12615974 12615981 TGCACACCCACAAACACACCTATACAGACACAACACACATGCACACATACACACCTATGCGCACA TGCACACCCACAAACACACCTATACAGACACA_______TGCACACATACACACCTATGCGCACA ATGTGTGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:12615980..12616092 26863196 MeRIP-seq:(Medium) rs1346646171 Functional Loss DEL dbSNP153 33..39 33 - - - 95936 RMVar_ID_95936 Human_SNP_ID_422201672 m1A Human chr10 - 12615981 12615978 12615981 TGCACACCCACAAACACACCTATACAGACACAACACACATGCACACATACACACCTATGCGCACA TGCACACCCACAAACACACCTATACAGACACA___CACATGCACACATACACACCTATGCGCACA GTGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:12615980..12616092 26863196 MeRIP-seq:(Medium) rs1330707904 Functional Loss DEL dbSNP153 33..35 33 - - - 95937 RMVar_ID_95937 Human_SNP_ID_422201673 m1A Human chr10 - 12615981 12615981 12615981 TGCACACCCACAAACACACCTATACAGACACAACACACATGCACACATACACACCTATGCGCACA TGCACACCCACAAACACACCTATACAGACACAGCACACATGCACACATACACACCTATGCGCACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:12615980..12616092 26863196 MeRIP-seq:(Medium) rs1046896036 Functional Loss SNV dbSNP153 33..33 33 - - - 95938 RMVar_ID_95938 Human_SNP_ID_422218704 m1A Human chr10 - 12679632 12679632 12679632 ACCCAAAGCAGGAATGGATACACTGCACTTGCAGGGCATGAGGAAATTAGTTTGGTTGGGGCAGA ACCCAAAGCAGGAATGGATACACTGCACTTGCGGGGCATGAGGAAATTAGTTTGGTTGGGGCAGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:12679630..12679827 26863196 MeRIP-seq:(Medium) rs1175583938 Functional Loss SNV dbSNP153 33..33 33 - - - 95939 RMVar_ID_95939 Human_SNP_ID_422232791 m1A Human chr10 + 12731584 12731584 12731584 AGAGGAGGTAAGAGTTGGGTCTAACCAGAGCCATGGCTTTGCCAAGTAAATAAGACAGAAAGAAG AGAGGAGGTAAGAGTTGGGTCTAACCAGAGCCGTGGCTTTGCCAAGTAAATAAGACAGAAAGAAG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12731579..12731830 26863196 MeRIP-seq:(Medium) rs1323140543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15754,RMVar_hsa_circ_327239,RMVar_hsa_circ_337140,RMVar_hsa_circ_45785,RMVar_hsa_circ_142200 95940 RMVar_ID_95940 Human_SNP_ID_422232801 m1A Human chr10 + 12731621 12731621 12731621 TTTGCCAAGTAAATAAGACAGAAAGAAGAGGGACGGTGTATGGCAAGGAGCAGCAGTGATCAGCT TTTGCCAAGTAAATAAGACAGAAAGAAGAGGGTCGGTGTATGGCAAGGAGCAGCAGTGATCAGCT A T CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12731618..12731843 26863196 MeRIP-seq:(Medium) rs112592345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15754,RMVar_hsa_circ_327239,RMVar_hsa_circ_337140,RMVar_hsa_circ_45785,RMVar_hsa_circ_142200 95941 RMVar_ID_95941 Human_SNP_ID_422244371 m1A Human chr10 + 12771566 12771566 12771566 GAGGAAAGACAAGAGCAGGCTGAGGCGGGCAGAGAACAAAATAAGGGGAAGGGAAAGAAGCAGCA GAGGAAAGACAAGAGCAGGCTGAGGCGGGCAGCGAACAAAATAAGGGGAAGGGAAAGAAGCAGCA A C CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12771558..12771708 26863196 MeRIP-seq:(Medium) rs1487335216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15754,RMVar_hsa_circ_327239,RMVar_hsa_circ_327076,RMVar_hsa_circ_142202 95942 RMVar_ID_95942 Human_SNP_ID_422249324 m1A Human chr10 - 12789967 12789967 12789967 TCTGGCGACCAGCAGCGTCTGGCATAGCTGGCACTCACTATATGTTAGTGCAAAGTGTAGAAAAA TCTGGCGACCAGCAGCGTCTGGCATAGCTGGCGCTCACTATATGTTAGTGCAAAGTGTAGAAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:12789964..12790056 26863196 MeRIP-seq:(Medium) rs923477946 Functional Loss SNV dbSNP153 33..33 33 - - - 95943 RMVar_ID_95943 Human_SNP_ID_422257554 m1A Human chr10 + 12819732 12819732 12819732 CTGTTAGGCAGGGTGCTGAGGTTTGATTTTAGACAACCCAATCTGGTGGGAGATGGAGTGTGGGA CTGTTAGGCAGGGTGCTGAGGTTTGATTTTAGGCAACCCAATCTGGTGGGAGATGGAGTGTGGGA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:12819728..12819922 26863196 MeRIP-seq:(Medium) rs1487232257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142206,RMVar_hsa_circ_58129 95944 RMVar_ID_95944 Human_SNP_ID_422276196 m1A Human chr10 + 12889046 12889031 12889047 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGAC________________AGATAGATAGATAGATAGATAGATAGACAGA CGGACGGACGGACAGAT C AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) rs1363052341 Functional Loss DEL dbSNP153 19..34 33 - - - 95945 RMVar_ID_95945 Human_SNP_ID_422276211 m1A Human chr10 + 12889046 12889035 12889047 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGACGGAC____________AGATAGATAGATAGATAGATAGATAGACAGA CGGACGGACAGAT C AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) rs777730056 Functional Loss DEL dbSNP153 23..34 33 - - - 95946 RMVar_ID_95946 Human_SNP_ID_422276229 m1A Human chr10 + 12889046 12889039 12889047 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGACGGACGGAC________AGATAGATAGATAGATAGATAGATAGACAGA CGGACAGAT C AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) rs56178402 Functional Loss DEL dbSNP153 27..34 33 - - - 95947 RMVar_ID_95947 Human_SNP_ID_422276251 m1A Human chr10 + 12889046 12889042 12889047 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGACGGACGGACGGA_____AGATAGATAGATAGATAGATAGATAGACAGA ACAGAT A AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) rs1222686068 Functional Loss DEL dbSNP153 30..34 33 - - - 95948 RMVar_ID_95948 Human_SNP_ID_422276277 m1A Human chr10 + 12889046 12889046 12889046 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGACGGACGGACGGACAGCTAGATAGATAGATAGATAGATAGATAGACAGA A C AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) rs1325661954 Functional Loss SNV dbSNP153 33..33 33 - - - 95949 RMVar_ID_95949 Human_SNP_ID_422334267 m1A Human chr10 + 13100301 13100301 13100301 CAGTGACCCTGAGCGAAGCCAAGCCGGGCGGCAGGTGAGCCAGGGCAGGGGGCTGCAGCGGTGGG CAGTGACCCTGAGCGAAGCCAAGCCGGGCGGCGGGTGAGCCAGGGCAGGGGGCTGCAGCGGTGGG A G OPTN Ensembl:ENSG00000123240 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:13100251..13100300 32194978 MeRIP-seq:(Medium) rs1361921899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9361086,Human_RBP_ID_26316104,Human_RBP_ID_26802468 Human_Splice_Rec_1113175,Human_Splice_Rec_1113179,Human_Splice_Rec_1113187,Human_Splice_Rec_1113215,Human_Splice_Rec_1113241,Human_Splice_Rec_1113249,Human_Splice_Rec_1113279 95950 RMVar_ID_95950 Human_SNP_ID_422350869 m1A Human chr10 - 13161608 13161608 13161608 GGTCACACGCACGCCCGGGGCCCGCGCTCCTCACCCGATGCCGGGACGCCTTCTTCGTTCACAGC GGTCACACGCACGCCCGGGGCCCGCGCTCCTCGCCCGATGCCGGGACGCCTTCTTCGTTCACAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:13161597..13161827;chr10:13161597..13161828 26863196 MeRIP-seq:(Medium) rs993025084 Functional Loss SNV dbSNP153 33..33 33 - - - 95951 RMVar_ID_95951 Human_SNP_ID_422357791 m1A Human chr10 + 13188973 13188973 13188973 CGTGCGGATCTGCAGTCCACCTTCTCTGGAGGACGAATTCCAAAGAAGTTTGCCCGCAGAGGCAC CGTGCGGATCTGCAGTCCACCTTCTCTGGAGGTCGAATTCCAAAGAAGTTTGCCCGCAGAGGCAC A T MCM10 Ensembl:ENSG00000065328 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:13188922..13191339 32194978 MeRIP-seq:(Medium) rs761043156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1113340,Human_Splice_Rec_1113382,Human_Splice_Rec_1113418 RMVar_hsa_circ_2167,RMVar_hsa_circ_54356,RMVar_hsa_circ_81574,RMVar_hsa_circ_1610,RMVar_hsa_circ_142229,RMVar_hsa_circ_326838,RMVar_hsa_circ_79191,RMVar_hsa_circ_35190,RMVar_hsa_circ_81343,RMVar_hsa_circ_142233,RMVar_hsa_circ_142234,RMVar_hsa_circ_313307,RMVar_hsa_circ_50083,RMVar_hsa_circ_53096,RMVar_hsa_circ_142236,RMVar_hsa_circ_142235,RMVar_hsa_circ_142238,RMVar_hsa_circ_96426,RMVar_hsa_circ_46088,RMVar_hsa_circ_365383,RMVar_hsa_circ_86881,RMVar_hsa_circ_142239,RMVar_hsa_circ_312487,RMVar_hsa_circ_142237,RMVar_hsa_circ_351363,RMVar_hsa_circ_285682 95952 RMVar_ID_95952 Human_SNP_ID_422359421 m1A Human chr10 + 13195268 13195268 13195268 ACCAAAACTGAGTGCTTTAGCAGAAGCCAAAAAGGTAACTGGCATCTCTTCTCTTTAGCACTTGA ACCAAAACTGAGTGCTTTAGCAGAAGCCAAAAGGGTAACTGGCATCTCTTCTCTTTAGCACTTGA A G MCM10 Ensembl:ENSG00000065328 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:13195251..13195275 32194978 MeRIP-seq:(Medium) rs772452690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1113349,Human_Splice_Rec_1113391,Human_Splice_Rec_1113427,Human_Splice_Rec_1113439 RMVar_hsa_circ_2167,RMVar_hsa_circ_1610,RMVar_hsa_circ_79191,RMVar_hsa_circ_35190,RMVar_hsa_circ_142234,RMVar_hsa_circ_313307,RMVar_hsa_circ_50083,RMVar_hsa_circ_53096,RMVar_hsa_circ_142236,RMVar_hsa_circ_142238,RMVar_hsa_circ_96426,RMVar_hsa_circ_46088,RMVar_hsa_circ_365383,RMVar_hsa_circ_38074,RMVar_hsa_circ_142239,RMVar_hsa_circ_351363,RMVar_hsa_circ_285682,RMVar_hsa_circ_342041,RMVar_hsa_circ_44553,RMVar_hsa_circ_142241,RMVar_hsa_circ_50635,RMVar_hsa_circ_347896,RMVar_hsa_circ_353390,RMVar_hsa_circ_313582,RMVar_hsa_circ_142242 95953 RMVar_ID_95953 Human_SNP_ID_422403115 m1A Human chr10 - 13347310 13347310 13347310 CTCCCCGGCCGCCTCCGACGCGGGCGTCCTGGAGAGCGCGCCCCATTGTGCGGGGCCGGCGGGGA CTCCCCGGCCGCCTCCGACGCGGGCGTCCTGGCGAGCGCGCCCCATTGTGCGGGGCCGGCGGGGA T G SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr10:13347307..13348272;chr10:13347307..13348106 26863196,32194978 MeRIP-seq:(Medium) rs112804918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374105,Human_RBP_ID_18456029 Human_Splice_Rec_1113581 95954 RMVar_ID_95954 Human_SNP_ID_422403199 m1A Human chr10 + 13347510 13347490 13347510 CATCCCTGTTCGGGCCGGCGGGAGGCGGCGGGAGCCGGCGGGCACCGCGCGTGCGGCCCAGGAGC CATCCCTGTTCGG____________________GCCGGCGGGCACCGCGCGTGCGGCCCAGGAGC GGCCGGCGGGAGGCGGCGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:13347496..13347629 26863196 MeRIP-seq:(Medium) rs1306527164 Functional Loss DEL dbSNP153 14..33 33 - - - 95955 RMVar_ID_95955 Human_SNP_ID_422403413 m1A Human chr10 + 13347829 13347829 13347829 CGCGGGCGGCGCTTCTTTTTTAAAGCGGCCCCACCAAGCCCGGCGCTGCCCCTCTCCAGGCAGGG CGCGGGCGGCGCTTCTTTTTTAAAGCGGCCCCCCCAAGCCCGGCGCTGCCCCTCTCCAGGCAGGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:13347821..13348117 26863196 MeRIP-seq:(Medium) rs1159033780 Functional Loss SNV dbSNP153 33..33 33 - - - 95956 RMVar_ID_95956 Human_SNP_ID_422403589 m1A Human chr10 - 13348188 13348188 13348188 AGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCAGGGCCGCGCCGAGGCAGGCGAGCCCCCGCGGC AGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCTGGGCCGCGCCGAGGCAGGCGAGCCCCCGCGGC T A SEPHS1 Ensembl:ENSG00000086475 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:13348098..13348298 26863410 MeRIP-seq:(Medium) rs1049013031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135764 95957 RMVar_ID_95957 Human_SNP_ID_422403615 m1A Human chr10 - 13348220 13348220 13348220 GGTGGCCGGCCTTAAAGGACCCCCGCGCGCCCAGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCA GGTGGCCGGCCTTAAAGGACCCCCGCGCGCCCTGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCA T A SEPHS1 Ensembl:ENSG00000086475 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:13348090..13348237 26863196 MeRIP-seq:(Medium) rs977046134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135764 95958 RMVar_ID_95958 Human_SNP_ID_422403616 m1A Human chr10 - 13348220 13348220 13348220 GGTGGCCGGCCTTAAAGGACCCCCGCGCGCCCAGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCA GGTGGCCGGCCTTAAAGGACCCCCGCGCGCCCCGCCGGCGGGAGCGCGGCGGCCCGGCTCCCGCA T G SEPHS1 Ensembl:ENSG00000086475 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:13348090..13348237 26863196 MeRIP-seq:(Medium) rs977046134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135764 95959 RMVar_ID_95959 Human_SNP_ID_422403629 m1A Human chr10 + 13348240 13348240 13348240 GCTCCCGCCGGCTGGGCGCGCGGGGGTCCTTTAAGGCCGGCCACCTCCCTTTAAGAGGCGGCCCT GCTCCCGCCGGCTGGGCGCGCGGGGGTCCTTTGAGGCCGGCCACCTCCCTTTAAGAGGCGGCCCT A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr10:13348147..13348298 26863410 MeRIP-seq:(Medium) rs1405084473 Functional Loss SNV dbSNP153 33..33 33 - - - 95960 RMVar_ID_95960 Human_SNP_ID_422451188 m1A Human chr10 + 13528590 13528548 13528590 GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG _________________________________GCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GGCGGCGGGGGCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCA G AL590677.2 Ensembl:ENSG00000227175 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:13528552..13528660 32194978 MeRIP-seq:(Medium) rs1564433301 Functional Loss DEL dbSNP153 1..33 33 - - - Human_Splice_Rec_1113677 95961 RMVar_ID_95961 Human_SNP_ID_422451203 m1A Human chr10 + 13528590 13528566 13528590 GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GCTGAGGAG________________________GCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GGCGGCGGCAGCGGCGGCAGCGGCA G AL590677.2 Ensembl:ENSG00000227175 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:13528552..13528660 32194978 MeRIP-seq:(Medium) rs765574643 Functional Loss DEL dbSNP153 10..33 33 - - - Human_Splice_Rec_1113677 95962 RMVar_ID_95962 Human_SNP_ID_422451229 m1A Human chr10 + 13528590 13528581 13528590 GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GCTGAGGAGGCGGCGGCAGCGGCG_________GCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GGCAGCGGCA G AL590677.2 Ensembl:ENSG00000227175 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:13528552..13528660 32194978 MeRIP-seq:(Medium) rs1164977989 Functional Loss DEL dbSNP153 25..33 33 - - - Human_Splice_Rec_1113677 95963 RMVar_ID_95963 Human_SNP_ID_422451242 m1A Human chr10 + 13528590 13528587 13528590 GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GCTGAGGAGGCGGCGGCAGCGGCGGCAGCG___GCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GGCA G AL590677.2 Ensembl:ENSG00000227175 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:13528552..13528660 32194978 MeRIP-seq:(Medium) rs1267643570 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_1113677 95964 RMVar_ID_95964 Human_SNP_ID_422451246 m1A Human chr10 + 13528590 13528590 13528590 GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG GCTGAGGAGGCGGCGGCAGCGGCGGCAGCGGCGGCGGCGGCAGCGGCAGCGGCGGCGCGGGCTCG A G AL590677.2 Ensembl:ENSG00000227175 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:13528552..13528660 32194978 MeRIP-seq:(Medium) rs187129301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1113677 95965 RMVar_ID_95965 Human_SNP_ID_422466254 m1A Human chr10 + 13587047 13587047 13587047 CGGCCGCCGGCCCAGTGAGGCTGGGTTCGAGGAGCTGGAGCGGGAAACTGGAGCTTAAATTCTGG CGGCCGCCGGCCCAGTGAGGCTGGGTTCGAGGCGCTGGAGCGGGAAACTGGAGCTTAAATTCTGG A C PRPF18 Ensembl:ENSG00000165630 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:13586996..13587195;chr10:13586998..13600332 26863196 MeRIP-seq:(Medium) rs1343253833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136167,Human_RBP_ID_5948558,Human_RBP_ID_8985472 95966 RMVar_ID_95966 Human_SNP_ID_422466256 m1A Human chr10 - 13587050 13587050 13587050 CCGCCAGAATTTAAGCTCCAGTTTCCCGCTCCAGCTCCTCGAACCCAGCCTCACTGGGCCGGCGG CCGCCAGAATTTAAGCTCCAGTTTCCCGCTCCTGCTCCTCGAACCCAGCCTCACTGGGCCGGCGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:13586999..13587201 26863196 MeRIP-seq:(Medium) rs779150942 Functional Loss SNV dbSNP153 33..33 33 - - - 95967 RMVar_ID_95967 Human_SNP_ID_422725442 m1A Human chr10 - 14530517 14530517 14530517 CTGCAAATGAGTGTTTCTCATCTTTCTCTTTCAGACAGCCCACCTGAGGATATTGACCATAAGGA CTGCAAATGAGTGTTTCTCATCTTTCTCTTTCGGACAGCCCACCTGAGGATATTGACCATAAGGA T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:14530492..14530563 26863196 MeRIP-seq:(Medium) rs112309992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862187,Human_RBP_ID_19046216 RMVar_hsa_circ_58870,RMVar_hsa_circ_285331 95968 RMVar_ID_95968 Human_SNP_ID_422740265 m1A Human chr10 + 14585273 14585273 14585273 AATTCTTTGTTCAAAATGCCAAGAACCTGGACACCCTCCACTAGTAACACCTGGACCCCACCTCA AATTCTTTGTTCAAAATGCCAAGAACCTGGACCCCCTCCACTAGTAACACCTGGACCCCACCTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:14585271..14585427 26863196 MeRIP-seq:(Medium) rs983607749 Functional Loss SNV dbSNP153 33..33 33 - - - 95969 RMVar_ID_95969 Human_SNP_ID_422740485 m1A Human chr10 - 14586132 14586132 14586132 ACTAGCACATGAGGAATTCGGGTCAGGAGGTCACCAGTAACCAGGAGTTGACAGTGATGCGGACT ACTAGCACATGAGGAATTCGGGTCAGGAGGTCCCCAGTAACCAGGAGTTGACAGTGATGCGGACT T G FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:14586128..14586248 26863196 MeRIP-seq:(Medium) rs7478628 Functional Loss SNV dbSNP153 33..33 33 - - - 95970 RMVar_ID_95970 Human_SNP_ID_422743074 m1A Human chr10 - 14595840 14595840 14595840 GGGTGCCGCTGGTGAGATGGATTGGAGTTGATACAAGAGAGAAAGGCATTGTGGGTGACACCTGC GGGTGCCGCTGGTGAGATGGATTGGAGTTGATGCAAGAGAGAAAGGCATTGTGGGTGACACCTGC T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:14595830..14595928 26863196 MeRIP-seq:(Medium) rs1010093768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11317480 95971 RMVar_ID_95971 Human_SNP_ID_422744411 m1A Human chr10 - 14600871 14600871 14600871 CTCAGGAGGCTGAGGCAGGTGGAATGCTTGTGACCAAGAGTTTGAGACCAGGCTGGGCAACATAG CTCAGGAGGCTGAGGCAGGTGGAATGCTTGTGGCCAAGAGTTTGAGACCAGGCTGGGCAACATAG T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:14600869..14600983 32194978 MeRIP-seq:(Medium) rs540168574 Functional Loss SNV dbSNP153 33..33 33 - - - 95972 RMVar_ID_95972 Human_SNP_ID_422745210 m1A Human chr10 + 14603725 14603721 14603725 ACAGGGGAGAAAGAGAAGAGGCAAAAGAGGAAAAGTTACTTGCAGACTGGAGTCAGTGTCACGGC ACAGGGGAGAAAGAGAAGAGGCAAAAGAG____AGTTACTTGCAGACTGGAGTCAGTGTCACGGC GGAAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:14603721..14603827 26863196 MeRIP-seq:(Medium) rs368972069 Functional Loss DEL dbSNP153 30..33 33 - - - 95973 RMVar_ID_95973 Human_SNP_ID_422745333 m1A Human chr10 - 14604037 14604037 14604037 CCCCGCGCGGCGCCCGGGAGGTGCCGGGGCTCAGGGCGGGCACGCGGCGGGGCCGTGCGGGGGGC CCCCGCGCGGCGCCCGGGAGGTGCCGGGGCTCGGGGCGGGCACGCGGCGGGGCCGTGCGGGGGGC T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:14604035..14604129 26863196 MeRIP-seq:(Medium) rs1361110763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862189,Human_RBP_ID_3363829,Human_RBP_ID_8172111,Human_RBP_ID_18456036,Human_RBP_ID_26775156 95974 RMVar_ID_95974 Human_SNP_ID_422818738 m1A Human chr10 - 14878456 14878456 14878456 CCGGGGACGCTGCCTGTCGGGTACGGTTCCGCAGCTACCGCAGCCCCGTGGGCCATGGTTAGTCT CCGGGGACGCTGCCTGTCGGGTACGGTTCCGCCGCTACCGCAGCCCCGTGGGCCATGGTTAGTCT T G AC069544.1 Ensembl:ENSG00000272853 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:14878386..14878536 26863196 MeRIP-seq:(Medium) rs1295398874 Functional Loss SNV dbSNP153 33..33 33 - - - 95975 RMVar_ID_95975 Human_SNP_ID_422818947 m1A Human chr10 + 14878918 14878918 14878918 AAGATGGCGGCGGTCGGGGCCGAGGCGCGAGGAGGTGAGGCTGGAGCGCGGCCCCCTCGCCTTCC AAGATGGCGGCGGTCGGGGCCGAGGCGCGAGGTGGTGAGGCTGGAGCGCGGCCCCCTCGCCTTCC A T SUV39H2 Ensembl:ENSG00000152455 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:14878904..14879065 26863196 MeRIP-seq:(Medium) rs1405468117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4114268,Human_RBP_ID_19045223 Human_Splice_Rec_1114649,Human_Splice_Rec_1114665,Human_Splice_Rec_1114675 95976 RMVar_ID_95976 Human_SNP_ID_422821459 m1A Human chr10 - 14887878 14887878 14887878 CATATCCCTTTCTTCCTTTAGTACTAAGTTGAAACATCAGTTCCTCAGGGATACCTGCCCAGTCT CATATCCCTTTCTTCCTTTAGTACTAAGTTGAGACATCAGTTCCTCAGGGATACCTGCCCAGTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:14887876..14888095 26863196 MeRIP-seq:(Medium) rs1460118431 Functional Loss SNV dbSNP153 33..33 33 - - - 95977 RMVar_ID_95977 Human_SNP_ID_422821467 m1A Human chr10 + 14887915 14887914 14887915 CTTAGTACTAAAGGAAGAAAGGGATATGTGGGAGGGATTTCGAGGCAGAAGACAGCCTGACTTCA CTTAGTACTAAAGGAAGAAAGGGATATGTGGG_GGGATTTCGAGGCAGAAGACAGCCTGACTTCA GA G SUV39H2 Ensembl:ENSG00000152455 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:14887911..14888021 26863196 MeRIP-seq:(Medium) rs780773118 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_55606 95978 RMVar_ID_95978 Human_SNP_ID_315295804 m1A Human chr7 - 30028457 30028457 30028457 ACGTGGGTCGGAGGGGCAGCCGAAGCCTCCAAAGTGCGGCGAACGAGCTGCCGGTCGCAGGCGGC ACGTGGGTCGGAGGGGCAGCCGAAGCCTCCAAGGTGCGGCGAACGAGCTGCCGGTCGCAGGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:30028407..30028481 26863196 MeRIP-seq:(Medium) rs1442105186 Functional Loss SNV dbSNP153 33..33 33 - - - 95979 RMVar_ID_95979 Human_SNP_ID_315295901 m1A Human chr7 + 30028720 30028720 30028720 GCTGGTGCTCCTCGCCTCTTGGGGCCTGGGGCAGTGAGGGGGCCGGCGGGCGTGGGCCGAGTGGC GCTGGTGCTCCTCGCCTCTTGGGGCCTGGGGCGGTGAGGGGGCCGGCGGGCGTGGGCCGAGTGGC A G PLEKHA8 Ensembl:ENSG00000106086 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:30028671..30028756 26863196 MeRIP-seq:(Medium) rs1299953353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955712,Human_RBP_ID_5242984,Human_RBP_ID_24211305 Human_Splice_Rec_853137,Human_Splice_Rec_853161,Human_Splice_Rec_853183,Human_Splice_Rec_853215,Human_Splice_Rec_853239,Human_Splice_Rec_853263,Human_Splice_Rec_853285 95980 RMVar_ID_95980 Human_SNP_ID_315322584 m1A Human chr7 + 30135046 30135046 30135046 CCGGCCCAGCCCGGCCCCGGAGGAGCCCGCGCAGGCCGAGCCGAGCGCCGCGCTGCCCGCCCGGG CCGGCCCAGCCCGGCCCCGGAGGAGCCCGCGCGGGCCGAGCCGAGCGCCGCGCTGCCCGCCCGGG A G MTURN Ensembl:ENSG00000180354 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:30134909..30135193;chr7:30134927..30135209 26863196 MeRIP-seq:(Medium) rs111931501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337746 Human_miRNA_ID_2250005 RMVar_hsa_circ_118245,RMVar_hsa_circ_244320 95981 RMVar_ID_95981 Human_SNP_ID_315322587 m1A Human chr7 + 30135052 30135052 30135052 CAGCCCGGCCCCGGAGGAGCCCGCGCAGGCCGAGCCGAGCGCCGCGCTGCCCGCCCGGGAGGAGG CAGCCCGGCCCCGGAGGAGCCCGCGCAGGCCGCGCCGAGCGCCGCGCTGCCCGCCCGGGAGGAGG A C MTURN Ensembl:ENSG00000180354 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:30134983..30135178 26863196 MeRIP-seq:(Medium) rs1422531866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118245,RMVar_hsa_circ_244320 95982 RMVar_ID_95982 Human_SNP_ID_315322593 m1A Human chr7 + 30135057 30135057 30135057 CGGCCCCGGAGGAGCCCGCGCAGGCCGAGCCGAGCGCCGCGCTGCCCGCCCGGGAGGAGGGCGCC CGGCCCCGGAGGAGCCCGCGCAGGCCGAGCCGGGCGCCGCGCTGCCCGCCCGGGAGGAGGGCGCC A G MTURN Ensembl:ENSG00000180354 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:30135014..30135186 26863196 MeRIP-seq:(Medium) rs893440199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118245,RMVar_hsa_circ_244320 95983 RMVar_ID_95983 Human_SNP_ID_315322641 m1A Human chr7 + 30135147 30135147 30135147 GGGAGGCGGGCGCGGGGCCGCGATGGATTTCCAGCAGCTGGCCGACGTTGCGGAGAAATGGTGCT GGGAGGCGGGCGCGGGGCCGCGATGGATTTCCGGCAGCTGGCCGACGTTGCGGAGAAATGGTGCT A G MTURN Ensembl:ENSG00000180354 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:30135046..30135225 26863410 MeRIP-seq:(Medium) rs755200249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682913,Human_RBP_ID_4962931,Human_RBP_ID_5153188,Human_RBP_ID_5327823,Human_RBP_ID_9337096,Human_RBP_ID_18426607 RMVar_hsa_circ_118245,RMVar_hsa_circ_244320 95984 RMVar_ID_95984 Human_SNP_ID_315326384 m1A Human chr7 - 30148614 30148614 30148614 TGGGTCTACTCTCAAGGTATCTCCAGAATCCAACCCCTCACCCCGCCTCTGCCGTGACCGTCCCA TGGGTCTACTCTCAAGGTATCTCCAGAATCCACCCCCTCACCCCGCCTCTGCCGTGACCGTCCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:30148612..30148737 26863196 MeRIP-seq:(Medium) rs1010384656 Functional Loss SNV dbSNP153 33..33 33 - - - 95985 RMVar_ID_95985 Human_SNP_ID_315357238 m1A Human chr7 - 30285707 30285707 30285707 GGCCGCCGCCGCCGTCCTCAGGGCTGCTGTGCACCGAGTCCTGCGAGCCGTACGGGCCGCTGCTG GGCCGCCGCCGCCGTCCTCAGGGCTGCTGTGCCCCGAGTCCTGCGAGCCGTACGGGCCGCTGCTG T G LOC105375218,LOC105375218:2,KR024019,KR024019:2 RNACentral:URS0000D5DC3E,RNACentral:URS0000A76402,RNACentral:URS00009D522A,RNACentral:URS0000A37485 lincRNA,lincRNA,Other,Other intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:30285603..30285778 26863196 MeRIP-seq:(Medium) rs1468987960 Functional Loss SNV dbSNP153 33..33 33 - - - 95986 RMVar_ID_95986 Human_SNP_ID_315406422 m1A Human chr7 - 30472218 30472218 30472218 GAGCTAAATAATGAGACACACTCAGGCCAAGTAGGGCCTCCTGGGCTGGGTAAGGATTTGGGATT GAGCTAAATAATGAGACACACTCAGGCCAAGTGGGGCCTCCTGGGCTGGGTAAGGATTTGGGATT T C NOD1 Ensembl:ENSG00000106100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:30472214..30472331 26863196 MeRIP-seq:(Medium) rs1229067569 Functional Loss SNV dbSNP153 33..33 33 - - - 95987 RMVar_ID_95987 Human_SNP_ID_315414423 m1A Human chr7 - 30504626 30504626 30504626 CTGTACTTTGCCTACGGCAGCAACCTGCTGACAGAGAGGATCCACCTCCGAAACCCCTCGGCGGC CTGTACTTTGCCTACGGCAGCAACCTGCTGACGGAGAGGATCCACCTCCGAAACCCCTCGGCGGC T C GGCT,AC005154.5 Ensembl:ENSG00000006625,Ensembl:ENSG00000281039 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:30504551..30504625 26863196 MeRIP-seq:(Medium) rs372620093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_683069,Human_RBP_ID_8666069,Human_RBP_ID_22322692,Human_RBP_ID_23215460 Human_Splice_Rec_853455,Human_Splice_Rec_853459,Human_Splice_Rec_853465,Human_Splice_Rec_853469,Human_Splice_Rec_853477,Human_Splice_Rec_853483,Human_Splice_Rec_853489 95988 RMVar_ID_95988 Human_SNP_ID_315419270 m1A Human chr7 - 30525921 30525921 30525921 TGACTTTGGGTGGGTGACTCCCGGGGTTTCCCACTCCATTACTGGGCCCTCACCTCCTGCTACCC TGACTTTGGGTGGGTGACTCCCGGGGTTTCCCGCTCCATTACTGGGCCCTCACCTCCTGCTACCC T C GARS1-DT,AC005154.5 Ensembl:ENSG00000196295,Ensembl:ENSG00000281039 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:30525873..30526040 26863196 MeRIP-seq:(Medium) rs1220796483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244350,RMVar_hsa_circ_355994,RMVar_hsa_circ_325997,RMVar_hsa_circ_244349 95989 RMVar_ID_95989 Human_SNP_ID_315419271 m1A Human chr7 - 30525921 30525921 30525921 TGACTTTGGGTGGGTGACTCCCGGGGTTTCCCACTCCATTACTGGGCCCTCACCTCCTGCTACCC TGACTTTGGGTGGGTGACTCCCGGGGTTTCCCCCTCCATTACTGGGCCCTCACCTCCTGCTACCC T G GARS1-DT,AC005154.5 Ensembl:ENSG00000196295,Ensembl:ENSG00000281039 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:30525873..30526040 26863196 MeRIP-seq:(Medium) rs1220796483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244350,RMVar_hsa_circ_355994,RMVar_hsa_circ_325997,RMVar_hsa_circ_244349 95990 RMVar_ID_95990 Human_SNP_ID_315426944 m1A Human chr7 + 30559627 30559627 30559627 ATCCACACTTACAGGAAAATCTAAAGAACTCAATGTGACTTACACAGCCCTGTATGTTCTGGCCC ATCCACACTTACAGGAAAATCTAAAGAACTCAGTGTGACTTACACAGCCCTGTATGTTCTGGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:30559379..30559705 26863196 MeRIP-seq:(Medium) rs1466671211 Functional Loss SNV dbSNP153 33..33 33 - - - 95991 RMVar_ID_95991 Human_SNP_ID_315435257 m1A Human chr7 - 30594947 30594947 30594947 GCAGCAGCAGCAGAGCGGCGCGAGCACCTCTAAGCAGCACTGGACGCGGAGAGGGCATGAGCCTG GCAGCAGCAGCAGAGCGGCGCGAGCACCTCTAGGCAGCACTGGACGCGGAGAGGGCATGAGCCTG T C GARS1-DT Ensembl:ENSG00000196295 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:30594851..30595244;chr7:30594876..30595191 26863196 MeRIP-seq:(Medium) rs773138162 Functional Loss SNV dbSNP153 33..33 33 - - - 95992 RMVar_ID_95992 Human_SNP_ID_315435258 m1A Human chr7 - 30594947 30594947 30594947 GCAGCAGCAGCAGAGCGGCGCGAGCACCTCTAAGCAGCACTGGACGCGGAGAGGGCATGAGCCTG GCAGCAGCAGCAGAGCGGCGCGAGCACCTCTACGCAGCACTGGACGCGGAGAGGGCATGAGCCTG T G GARS1-DT Ensembl:ENSG00000196295 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:30594851..30595244;chr7:30594876..30595191 26863196 MeRIP-seq:(Medium) rs773138162 Functional Loss SNV dbSNP153 33..33 33 - - - 95993 RMVar_ID_95993 Human_SNP_ID_315435308 m1A Human chr7 + 30595002 30595002 30595002 CTGCTGCTGCTGCCGCCCCGGCTCTTAGCCCGACCCTCGCTCCTGCTCCGCCGGTCCCTCAGCGC CTGCTGCTGCTGCCGCCCCGGCTCTTAGCCCGGCCCTCGCTCCTGCTCCGCCGGTCCCTCAGCGC A G GARS1 Ensembl:ENSG00000106105 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr7:30594876..30595100;chr7:30594925..30595007 26863196,26863410 MeRIP-seq:(Medium) rs1230805729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_683098,Human_RBP_ID_793017,Human_RBP_ID_4956257,Human_RBP_ID_5513266,Human_RBP_ID_8271903,Human_RBP_ID_9337100,Human_RBP_ID_22112297,Human_RBP_ID_22534247,Human_RBP_ID_27531246 Human_miRNA_ID_2579628 RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_106627,RMVar_hsa_circ_244361,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363 95994 RMVar_ID_95994 Human_SNP_ID_315436301 m1A Human chr7 - 30598845 30598845 30598845 TGCGGGCTTTGAGCTCAGCCACTGCTTTGTCTACGTCTACTTGGGGTGCTTTATCTTCTTTGAGT TGCGGGCTTTGAGCTCAGCCACTGCTTTGTCTGCGTCTACTTGGGGTGCTTTATCTTCTTTGAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:30598740..30598948 26863196 MeRIP-seq:(Medium) rs758964807 Functional Loss SNV dbSNP153 33..33 33 - - - 95995 RMVar_ID_95995 Human_SNP_ID_315436631 m1A Human chr7 + 30599999 30599999 30599999 AGATGATATTGTAGACCGAGCAAAAATGGAAGATACCCTGAAGAGGAGGTTTTTCTATGATCAAG AGATGATATTGTAGACCGAGCAAAAATGGAAGTTACCCTGAAGAGGAGGTTTTTCTATGATCAAG A T GARS1 Ensembl:ENSG00000106105 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:30599890..30599999 26863196 MeRIP-seq:(Medium) rs766540026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_683103,Human_RBP_ID_1686052,Human_RBP_ID_2041482,Human_RBP_ID_3843971,Human_RBP_ID_7732188,Human_RBP_ID_9210255,Human_RBP_ID_16137322,Human_RBP_ID_18099117,Human_RBP_ID_19019507,Human_RBP_ID_23076255,Human_RBP_ID_24211730 Human_Splice_Rec_853802,Human_Splice_Rec_853803,Human_Splice_Rec_853810,Human_Splice_Rec_853811,Human_Splice_Rec_853840,Human_Splice_Rec_853841 Human_miRNA_ID_1137210,Human_miRNA_ID_1139726 RMVar_hsa_circ_11800,RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_106627,RMVar_hsa_circ_318343,RMVar_hsa_circ_244361,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363,RMVar_hsa_circ_337059,RMVar_hsa_circ_360671,RMVar_hsa_circ_322693,RMVar_hsa_circ_33073,RMVar_hsa_circ_33440,RMVar_hsa_circ_25027,RMVar_hsa_circ_61702,RMVar_hsa_circ_244364,RMVar_hsa_circ_244365,RMVar_hsa_circ_94406,RMVar_hsa_circ_374938,RMVar_hsa_circ_244366,RMVar_hsa_circ_244367 95996 RMVar_ID_95996 Human_SNP_ID_315450285 m1A Human chr7 + 30655735 30655735 30655735 CTTCACTGCCTTCCTGGGGGCGAGAGGTGGACACAGGTCTGAGCCCATGCGGCAGGCAGGGCCTC CTTCACTGCCTTCCTGGGGGCGAGAGGTGGACCCAGGTCTGAGCCCATGCGGCAGGCAGGGCCTC A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:30655684..30655780 26863196 MeRIP-seq:(Medium) rs1464700362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1686169,Human_RBP_ID_16138968 95997 RMVar_ID_95997 Human_SNP_ID_315904258 m1A Human chr7 + 32490348 32490348 32490348 TTACCTAAGGGCAGCAGCTGCGACGGGTTGGTAGTAGCGTTAGCCGCCATGGCTACGCCGGAAGT TTACCTAAGGGCAGCAGCTGCGACGGGTTGGTGGTAGCGTTAGCCGCCATGGCTACGCCGGAAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:32490264..32490348 26863196 MeRIP-seq:(Medium) rs1337350505 Functional Loss SNV dbSNP153 33..33 33 - - - 95998 RMVar_ID_95998 Human_SNP_ID_315904260 m1A Human chr7 - 32490350 32490350 32490350 CCACTTCCGGCGTAGCCATGGCGGCTAACGCTACTACCAACCCGTCGCAGCTGCTGCCCTTAGGT CCACTTCCGGCGTAGCCATGGCGGCTAACGCTTCTACCAACCCGTCGCAGCTGCTGCCCTTAGGT T A LSM5 Ensembl:ENSG00000106355 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:32490189..32490349 26863196 MeRIP-seq:(Medium) rs761552063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4939511,Human_RBP_ID_5479546,Human_RBP_ID_9337101,Human_RBP_ID_17541134,Human_RBP_ID_21904438,Human_RBP_ID_22463045,Human_RBP_ID_26357685 Human_Splice_Rec_854927,Human_Splice_Rec_854959,Human_Splice_Rec_854973,Human_Splice_Rec_854991 RMVar_hsa_circ_244419 95999 RMVar_ID_95999 Human_SNP_ID_315904261 m1A Human chr7 - 32490350 32490350 32490350 CCACTTCCGGCGTAGCCATGGCGGCTAACGCTACTACCAACCCGTCGCAGCTGCTGCCCTTAGGT CCACTTCCGGCGTAGCCATGGCGGCTAACGCTGCTACCAACCCGTCGCAGCTGCTGCCCTTAGGT T C LSM5 Ensembl:ENSG00000106355 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:32490189..32490349 26863196 MeRIP-seq:(Medium) rs761552063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4939511,Human_RBP_ID_5479546,Human_RBP_ID_9337101,Human_RBP_ID_17541134,Human_RBP_ID_21904438,Human_RBP_ID_22463045,Human_RBP_ID_26357685 Human_Splice_Rec_854927,Human_Splice_Rec_854959,Human_Splice_Rec_854973,Human_Splice_Rec_854991 RMVar_hsa_circ_244419 96000 RMVar_ID_96000 Human_SNP_ID_315905723 m1A Human chr7 - 32495711 32495711 32495711 GGACGCCATCCCCGCCTCTCCTGGCCTTCTCCATGGGCGGCCGCCGCGGGCCCGCACGACGACTT GGACGCCATCCCCGCCTCTCCTGGCCTTCTCCTTGGGCGGCCGCCGCGGGCCCGCACGACGACTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:32495662..32495740 26863196 MeRIP-seq:(Medium) rs941503834 Functional Loss SNV dbSNP153 33..33 33 - - - 96001 RMVar_ID_96001 Human_SNP_ID_315910257 m1A Human chr7 + 32512251 32512251 32512251 AGGCAAAGATTGATCAAGGGGCTAACAGAGGCAGGGGCTTGGGGCCTAGGAGAGCAGTTCTGAAG AGGCAAAGATTGATCAAGGGGCTAACAGAGGCGGGGGCTTGGGGCCTAGGAGAGCAGTTCTGAAG A G AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:32512248..32512361 32194978 MeRIP-seq:(Medium) rs950860575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7732974 RMVar_hsa_circ_244420,RMVar_hsa_circ_113624 96002 RMVar_ID_96002 Human_SNP_ID_315967374 m1A Human chr7 + 32728179 32728179 32728179 GAGGATGGCGGCGGTAACAGCGGCCGCCGGAGAGGAGGCGGTGGGGAGGCCCGGGGCGCCAAGCG GAGGATGGCGGCGGTAACAGCGGCCGCCGGAGTGGAGGCGGTGGGGAGGCCCGGGGCGCCAAGCG A T lnc-AVL9-6 RNACentral:URS00008C40C2 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:32728130..32728254 26863196 MeRIP-seq:(Medium) rs971490180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96003 RMVar_ID_96003 Human_SNP_ID_315967551 m1A Human chr7 + 32728676 32728676 32728676 GTAGCAGCGGAGTGGCCAATGGGACCGGGACCAGGGCTGGGGGCCGGGGGGCCGCCGCCGCGGGG GTAGCAGCGGAGTGGCCAATGGGACCGGGACCTGGGCTGGGGGCCGGGGGGCCGCCGCCGCGGGG A T ZNRF2P1 Ensembl:ENSG00000237004 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:32728579..32728739 26863410 MeRIP-seq:(Medium) rs1457750908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253975,Human_RBP_ID_842854,Human_RBP_ID_955618,Human_RBP_ID_5327825,Human_RBP_ID_8272452,Human_RBP_ID_8730789,Human_RBP_ID_9337103,Human_RBP_ID_17674046,Human_RBP_ID_18927440,Human_RBP_ID_19139773 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96004 RMVar_ID_96004 Human_SNP_ID_315994453 m1A Human chr7 - 32840469 32840469 32840469 TTATCAACCAAATTGTTTTGCCTATCCACCCCATGGTGCCCAACCCATATATTCTCCTATCCTCA TTATCAACCAAATTGTTTTGCCTATCCACCCCGTGGTGCCCAACCCATATATTCTCCTATCCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:32840370..32840470 26863196 MeRIP-seq:(Medium) rs575353779 Functional Loss SNV dbSNP153 33..33 33 - - - 96005 RMVar_ID_96005 Human_SNP_ID_315994454 m1A Human chr7 - 32840469 32840469 32840469 TTATCAACCAAATTGTTTTGCCTATCCACCCCATGGTGCCCAACCCATATATTCTCCTATCCTCA TTATCAACCAAATTGTTTTGCCTATCCACCCCCTGGTGCCCAACCCATATATTCTCCTATCCTCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:32840370..32840470 26863196 MeRIP-seq:(Medium) rs575353779 Functional Loss SNV dbSNP153 33..33 33 - - - 96006 RMVar_ID_96006 Human_SNP_ID_315994948 m1A Human chr7 + 32841960 32841960 32841960 ATTGGGACCTAGCTTGGACTGGCGAGGAGGGGAGAGGTCAGATGGGTCTGTAGAAAAGGAAGATT ATTGGGACCTAGCTTGGACTGGCGAGGAGGGGGGAGGTCAGATGGGTCTGTAGAAAAGGAAGATT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:32841904..32842016 26863196 MeRIP-seq:(Medium) rs1350034058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89047,RMVar_hsa_circ_244430,RMVar_hsa_circ_244468,RMVar_hsa_circ_244469 96007 RMVar_ID_96007 Human_SNP_ID_316007453 m1A Human chr7 - 32891166 32891166 32891166 GCCTCGGCTCGCGCCCGCCCTTACCGAAGTAAAGCTGTTTCCCTTAAAGACTCGCGACGTGTTCG GCCTCGGCTCGCGCCCGCCCTTACCGAAGTAAGGCTGTTTCCCTTAAAGACTCGCGACGTGTTCG T C KBTBD2 Ensembl:ENSG00000170852 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:32891164..32891264 26863196 MeRIP-seq:(Medium) rs1368909257 Functional Loss SNV dbSNP153 33..33 33 - - - 96008 RMVar_ID_96008 Human_SNP_ID_316007747 m1A Human chr7 + 32891817 32891813 32891817 GGGCCCGACCACCGCCAGACTCCTCCCCCGGGAGCCGCGCCGCCCGCCCGCCCGCGCCGCCTTGT GGGCCCGACCACCGCCAGACTCCTCCCCC____GCCGCGCCGCCCGCCCGCCCGCGCCGCCTTGT CGGGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:32891732..32891885 26863410 MeRIP-seq:(Medium) rs1211943449 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96009 RMVar_ID_96009 Human_SNP_ID_316007754 m1A Human chr7 + 32891817 32891817 32891817 GGGCCCGACCACCGCCAGACTCCTCCCCCGGGAGCCGCGCCGCCCGCCCGCCCGCGCCGCCTTGT GGGCCCGACCACCGCCAGACTCCTCCCCCGGGGGCCGCGCCGCCCGCCCGCCCGCGCCGCCTTGT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:32891732..32891885 26863410 MeRIP-seq:(Medium) rs1192130752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96010 RMVar_ID_96010 Human_SNP_ID_316020987 m1A Human chr7 + 32942953 32942875 32942953 CGCTTCTGCTCCCGGGCCCGCTGCAGTTCCTGATCCAGCGGCTCCCGCGGCCACCACGCGCCCCC _________________________________TCCAGCGGCTCCCGCGGCCACCACGCGCCCCC CTCCAGGCGCTTGAGCTGCTGCAGCTGCTGGGCGTCGTGCCGCCGCCGCTTCTGCTCCCGGGCCCGCTGCAGTTCCTGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:32942848..32943200;chr7:32933856..32943200 26863196 MeRIP-seq:(Medium) rs1562555073 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96011 RMVar_ID_96011 Human_SNP_ID_316024799 m1A Human chr7 + 32957502 32957502 32957502 GGCCAGGAGACCCGGTCCACGTTTGCAAACGCAGCCGAACGCCCAGGCCGACCCGTGCCGCCCGA GGCCAGGAGACCCGGTCCACGTTTGCAAACGCGGCCGAACGCCCAGGCCGACCCGTGCCGCCCGA A G FKBP9 Ensembl:ENSG00000122642 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:32957453..32957603 26863196 MeRIP-seq:(Medium) rs1371893018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955724 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96012 RMVar_ID_96012 Human_SNP_ID_316024816 m1A Human chr7 - 32957548 32957548 32957548 ACGCCATCGGGGCGGCGAGAAGAGTGGCGCGGACGCAGCGCGGCGCTCGGGCGGCACGGGTCGGC ACGCCATCGGGGCGGCGAGAAGAGTGGCGCGGGCGCAGCGCGGCGCTCGGGCGGCACGGGTCGGC T C lnc-NT5C3A-3 RNACentral:URS0000D5BCEE lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:32957451..32957752 26863410 MeRIP-seq:(Medium) rs1056130812 Functional Loss SNV dbSNP153 33..33 33 - - - 96013 RMVar_ID_96013 Human_SNP_ID_316024897 m1A Human chr7 + 32957752 32957752 32957752 CACCGTGCGCAGCGGCGACTTCGTGCGCTACCACTACGTGGGGACGTTCCCCGACGGCCAGAAGT CACCGTGCGCAGCGGCGACTTCGTGCGCTACCTCTACGTGGGGACGTTCCCCGACGGCCAGAAGT A T FKBP9 Ensembl:ENSG00000122642 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:32957524..32957775 26863196 MeRIP-seq:(Medium) rs748391190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4963053,Human_RBP_ID_22463455 Human_Splice_Rec_855215,Human_Splice_Rec_855235,Human_Splice_Rec_855239,Human_Splice_Rec_855249,Human_Splice_Rec_855267 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430 96014 RMVar_ID_96014 Human_SNP_ID_316024901 m1A Human chr7 - 32957758 32957758 32957758 AGTCGAACTTCTGGCCGTCGGGGAACGTCCCCACGTAGTGGTAGCGCACGAAGTCGCCGCTGCGC AGTCGAACTTCTGGCCGTCGGGGAACGTCCCCGCGTAGTGGTAGCGCACGAAGTCGCCGCTGCGC T C lnc-NT5C3A-3 RNACentral:URS0000D5BCEE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:32957460..32957775 26863196 MeRIP-seq:(Medium) rs937200530 Functional Loss SNV dbSNP153 33..33 33 - - - 96015 RMVar_ID_96015 Human_SNP_ID_316032598 m1A Human chr7 + 32988626 32988624 32988626 TGGAGAAAAGCGAAGGATTGTGGTCCCGCCTCACCTGGGGTATGGAGAGGAAGGAAGAGGTGAGC TGGAGAAAAGCGAAGGATTGTGGTCCCGCCT__CCTGGGGTATGGAGAGGAAGGAAGAGGTGAGC TCA T FKBP9 Ensembl:ENSG00000122642 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:32988601..32988625 32194978 MeRIP-seq:(Medium) rs1405308090 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_957265,Human_RBP_ID_7733480,Human_RBP_ID_9354747,Human_RBP_ID_22774870,Human_RBP_ID_24212415 Human_Splice_Rec_855227,Human_Splice_Rec_855259,Human_Splice_Rec_855279,Human_Splice_Rec_855285,Human_Splice_Rec_855291,Human_Splice_Rec_855299,Human_Splice_Rec_855309,Human_Splice_Rec_855311 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430,RMVar_hsa_circ_40351,RMVar_hsa_circ_58345,RMVar_hsa_circ_306923,RMVar_hsa_circ_340938,RMVar_hsa_circ_244487,RMVar_hsa_circ_95462,RMVar_hsa_circ_360172,RMVar_hsa_circ_244488,RMVar_hsa_circ_41139,RMVar_hsa_circ_244490,RMVar_hsa_circ_93439,RMVar_hsa_circ_278686,RMVar_hsa_circ_334124,RMVar_hsa_circ_374182,RMVar_hsa_circ_103038,RMVar_hsa_circ_244491,RMVar_hsa_circ_244492,RMVar_hsa_circ_244489 96016 RMVar_ID_96016 Human_SNP_ID_316049779 m1A Human chr7 - 33058741 33058741 33058741 GGTTAAAGATAAGAGGAGGAGAAAAAATAATCAGTCTAGCAAAGTTCTAGGGGAGATGTGGACAG GGTTAAAGATAAGAGGAGGAGAAAAAATAATCGGTCTAGCAAAGTTCTAGGGGAGATGTGGACAG T C NT5C3A Ensembl:ENSG00000122643 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:33058731..33058898 26863196 MeRIP-seq:(Medium) rs1205610760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7733688,Human_RBP_ID_16142242 96017 RMVar_ID_96017 Human_SNP_ID_316062021 m1A Human chr7 + 33109366 33109364 33109367 CGCAGCCCCCACGTCCTCGCGCCCAGGCCGGGACGACATGTCAGCCCCCGCAGCGCCGCTCGGGC CGCAGCCCCCACGTCCTCGCGCCCAGGCCGG___GACATGTCAGCCCCCGCAGCGCCGCTCGGGC GGAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:33109226..33109574;chr7:33109260..33109592 26863196 MeRIP-seq:(Medium) rs1338506803 Functional Loss DEL dbSNP153 32..34 33 - - - 96018 RMVar_ID_96018 Human_SNP_ID_316250029 m1A Human chr7 + 33905167 33905167 33905167 CTGGCAGGAGGTGAGGAGTGCGGGAGTGGAGGACGCTGCGGCAGCGACAGCGACAGCCCCCGAAA CTGGCAGGAGGTGAGGAGTGCGGGAGTGGAGGCCGCTGCGGCAGCGACAGCGACAGCCCCCGAAA A C BMPER Ensembl:ENSG00000164619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:33905074..33905236 26863196 MeRIP-seq:(Medium) rs180818635 Functional Loss SNV dbSNP153 33..33 33 - - - 96019 RMVar_ID_96019 Human_SNP_ID_316345793 m1A Human chr7 + 34303020 34303020 34303020 AGGACGCAAAGGAGGCTTTGGATTGGGAAGAAAGGCAGCAATGAGATGTAGCTATAATCCAGGAA AGGACGCAAAGGAGGCTTTGGATTGGGAAGAAGGGCAGCAATGAGATGTAGCTATAATCCAGGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:34302974..34303047 26863196 MeRIP-seq:(Medium) rs1268604155 Functional Loss SNV dbSNP153 33..33 33 - - - 96020 RMVar_ID_96020 Human_SNP_ID_316522692 m1A Human chr7 + 35036917 35036917 35036917 GAGGAGAGCTGAGCCAGGGAGTTGCGGGGAGGAGAAGGTAAGAATGTCCCAGAGAAAAAGTCGGA GAGGAGAGCTGAGCCAGGGAGTTGCGGGGAGGGGAAGGTAAGAATGTCCCAGAGAAAAAGTCGGA A G AC005400.1 Ensembl:ENSG00000287249 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:35036866..35036948 26863196 MeRIP-seq:(Medium) rs762685291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_857215 96021 RMVar_ID_96021 Human_SNP_ID_316676642 m1A Human chr7 - 35694564 35694564 35694564 CCGGAGCCCGGCGGAGCCCGGACCTGGCGGGGAGAGCTGCCTCCACGGCCGGGCACCCAGACCCC CCGGAGCCCGGCGGAGCCCGGACCTGGCGGGGGGAGCTGCCTCCACGGCCGGGCACCCAGACCCC T C HERPUD2 Ensembl:ENSG00000122557 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:35694518..35694608 26863196 MeRIP-seq:(Medium) rs1016444678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253285,Human_RBP_ID_4957089 Human_Splice_Rec_857312,Human_Splice_Rec_857350,Human_Splice_Rec_857354 Human_miRNA_ID_2474945,Human_miRNA_ID_2960732 RMVar_hsa_circ_112727,RMVar_hsa_circ_111768,RMVar_hsa_circ_244609,RMVar_hsa_circ_378019,RMVar_hsa_circ_244614 96022 RMVar_ID_96022 Human_SNP_ID_316676728 m1A Human chr7 + 35694858 35694858 35694858 ACCGCCGCCCTCCGCGCCCAGGCAGGGCCGCCAGCCACACCGTCCGGCCAGGCGTTTTCCGTGGC ACCGCCGCCCTCCGCGCCCAGGCAGGGCCGCCGGCCACACCGTCCGGCCAGGCGTTTTCCGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:35694483..35695121 26863196 MeRIP-seq:(Medium) rs894635853 Functional Loss SNV dbSNP153 33..33 33 - - - 96023 RMVar_ID_96023 Human_SNP_ID_316676883 m1A Human chr7 - 35695263 35695263 35695263 CTAGAGTCCCGGGCAGCCCGAGCACGGCGGGAAGGCGGCAGCAACAGGATCGGCAGGGATGGCGG CTAGAGTCCCGGGCAGCCCGAGCACGGCGGGATGGCGGCAGCAACAGGATCGGCAGGGATGGCGG T A HERPUD2 Ensembl:ENSG00000122557 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:35695213..35695314 26863196 MeRIP-seq:(Medium) rs1200943052 Functional Loss SNV dbSNP153 33..33 33 - - - 96024 RMVar_ID_96024 Human_SNP_ID_316700148 m1A Human chr7 + 35801256 35801256 35801256 GAGATCCGCTGCTGCTGAGGAGAGGAGCGTCAACAGCAGCACCATGGGTGAGTCTCAGCTTCGGG GAGATCCGCTGCTGCTGAGGAGAGGAGCGTCAGCAGCAGCACCATGGGTGAGTCTCAGCTTCGGG A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:35801050..35801441;chr7:35801051..35801527 26863196 MeRIP-seq:(Medium) rs774176679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_683646,Human_RBP_ID_795008,Human_RBP_ID_4956276,Human_RBP_ID_18425989,Human_RBP_ID_19020660,Human_RBP_ID_23080536 Human_Splice_Rec_857463,Human_Splice_Rec_857469,Human_Splice_Rec_857515,Human_Splice_Rec_857537,Human_Splice_Rec_857547,Human_Splice_Rec_857565,Human_Splice_Rec_857569,Human_Splice_Rec_857615 96025 RMVar_ID_96025 Human_SNP_ID_316707558 m1A Human chr7 + 35831493 35831493 35831493 CTGGAATGATGGAAATGTGTTCTTTACAAAGTAGCTGTGAGTATACTACATAATTTATAGAGTTT CTGGAATGATGGAAATGTGTTCTTTACAAAGTTGCTGTGAGTATACTACATAATTTATAGAGTTT A T SEPTIN7 Ensembl:ENSG00000122545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:35831476..35831500 26863196 MeRIP-seq:(Medium) rs1201505663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19136211 Human_Splice_Rec_857464,Human_Splice_Rec_857465,Human_Splice_Rec_857538,Human_Splice_Rec_857539,Human_Splice_Rec_857557,Human_Splice_Rec_857566,Human_Splice_Rec_857581,Human_Splice_Rec_857591,Human_Splice_Rec_857616,Human_Splice_Rec_857617 RMVar_hsa_circ_41185,RMVar_hsa_circ_244624,RMVar_hsa_circ_361759,RMVar_hsa_circ_295838 96026 RMVar_ID_96026 Human_SNP_ID_316715954 m1A Human chr7 + 35868513 35868513 35868513 AGTGAGAAAGATGCTTTTGTAAGGTGCTGTAGAGGTGACCTTGGCAAGGTAAATTTTAATGAAGT AGTGAGAAAGATGCTTTTGTAAGGTGCTGTAGGGGTGACCTTGGCAAGGTAAATTTTAATGAAGT A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:35868509..35868684 26863196 MeRIP-seq:(Medium) rs1489347944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16145893 RMVar_hsa_circ_49503,RMVar_hsa_circ_329334,RMVar_hsa_circ_341210,RMVar_hsa_circ_244626 96027 RMVar_ID_96027 Human_SNP_ID_316721285 m1A Human chr7 + 35890740 35890740 35890740 CACTATGAGAACTACAGAAGCAGAAAACTTGCAGCTGTGACTTATAATGGAGTTGATAACAACAA CACTATGAGAACTACAGAAGCAGAAAACTTGCCGCTGTGACTTATAATGGAGTTGATAACAACAA A C SEPTIN7 Ensembl:ENSG00000122545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:35890728..35890853 26863196 MeRIP-seq:(Medium) rs1343888265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2042109,Human_RBP_ID_26356384 Human_Splice_Rec_857486,Human_Splice_Rec_857487,Human_Splice_Rec_857508,Human_Splice_Rec_857509,Human_Splice_Rec_857530,Human_Splice_Rec_857531,Human_Splice_Rec_857608,Human_Splice_Rec_857609,Human_Splice_Rec_857640,Human_Splice_Rec_857641,Human_Splice_Rec_857662,Human_Splice_Rec_857663,Human_Splice_Rec_857699,Human_Splice_Rec_857701 Human_miRNA_ID_2047187,Human_miRNA_ID_2248701 RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629,RMVar_hsa_circ_279187 96028 RMVar_ID_96028 Human_SNP_ID_316818175 m1A Human chr7 + 36284812 36284812 36284812 GGAAGCTGGCGGGCCCCAGCCCATACCTCGGGAGGTTCAAGGTACCCGCTCCACGCCGTCTGTGA GGAAGCTGGCGGGCCCCAGCCCATACCTCGGGCGGTTCAAGGTACCCGCTCCACGCCGTCTGTGA A C EEPD1 Ensembl:ENSG00000122547 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:36284730..36284885 26863410 MeRIP-seq:(Medium) rs768388217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19019528,Human_RBP_ID_19134761 Human_Splice_Rec_857751,Human_Splice_Rec_857765,Human_Splice_Rec_857773 RMVar_hsa_circ_244631,RMVar_hsa_circ_79699,RMVar_hsa_circ_329948,RMVar_hsa_circ_244630,RMVar_hsa_circ_283815,RMVar_hsa_circ_244632,RMVar_hsa_circ_87511 96029 RMVar_ID_96029 Human_SNP_ID_316818885 m1A Human chr7 - 36287594 36287594 36287594 AAACAAAGCAACAGGGAGAGGCTCAGAAGCTCATATTTCCTGTATCCGTTACAACCGACTCATAA AAACAAAGCAACAGGGAGAGGCTCAGAAGCTCTTATTTCCTGTATCCGTTACAACCGACTCATAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:36287586..36287705 26863196 MeRIP-seq:(Medium) rs368005491 Functional Loss SNV dbSNP153 33..33 33 - - - 96030 RMVar_ID_96030 Human_SNP_ID_316818886 m1A Human chr7 - 36287594 36287594 36287594 AAACAAAGCAACAGGGAGAGGCTCAGAAGCTCATATTTCCTGTATCCGTTACAACCGACTCATAA AAACAAAGCAACAGGGAGAGGCTCAGAAGCTCGTATTTCCTGTATCCGTTACAACCGACTCATAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:36287586..36287705 26863196 MeRIP-seq:(Medium) rs368005491 Functional Loss SNV dbSNP153 33..33 33 - - - 96031 RMVar_ID_96031 Human_SNP_ID_316843200 m1A Human chr7 - 36389900 36389900 36389900 CCAGGAGTCTGAGGCGGGGGAACTCTCCCACAACCAGCTGTCCTCTCCTCTCGGCTTCCAGTGAC CCAGGAGTCTGAGGCGGGGGAACTCTCCCACAGCCAGCTGTCCTCTCCTCTCGGCTTCCAGTGAC T C KIAA0895 Ensembl:ENSG00000164542 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:36389851..36390050 26863196 MeRIP-seq:(Medium) rs1014441719 Functional Loss SNV dbSNP153 33..33 33 - - - 96032 RMVar_ID_96032 Human_SNP_ID_316843205 m1A Human chr7 + 36389907 36389907 36389907 GAAGCCGAGAGGAGAGGACAGCTGGTTGTGGGAGAGTTCCCCCGCCTCAGACTCCTGGTTTTTTC GAAGCCGAGAGGAGAGGACAGCTGGTTGTGGGGGAGTTCCCCCGCCTCAGACTCCTGGTTTTTTC A G ANLN Ensembl:ENSG00000011426 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:36389851..36389979 26863196 MeRIP-seq:(Medium) rs886639581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254092,Human_RBP_ID_4955737,Human_RBP_ID_5153606,Human_RBP_ID_5533469,Human_RBP_ID_8666689,Human_RBP_ID_18426608,Human_RBP_ID_24213789 96033 RMVar_ID_96033 Human_SNP_ID_316843208 m1A Human chr7 - 36389912 36389912 36389912 TCCTGGAAAAAACCAGGAGTCTGAGGCGGGGGAACTCTCCCACAACCAGCTGTCCTCTCCTCTCG TCCTGGAAAAAACCAGGAGTCTGAGGCGGGGGGACTCTCCCACAACCAGCTGTCCTCTCCTCTCG T C KIAA0895 Ensembl:ENSG00000164542 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:36389865..36390100 26863196 MeRIP-seq:(Medium) rs992926972 Functional Loss SNV dbSNP153 33..33 33 - - - 96034 RMVar_ID_96034 Human_SNP_ID_316843237 m1A Human chr7 - 36389975 36389975 36389975 CGAGACGATGGAAACGGTGGTTCAAATTCAGGAAGAGAAAAGTGAGTCTCAGCTCAGTGTGTCTC CGAGACGATGGAAACGGTGGTTCAAATTCAGGGAGAGAAAAGTGAGTCTCAGCTCAGTGTGTCTC T C KIAA0895 Ensembl:ENSG00000164542 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:36389926..36390000 26863196 MeRIP-seq:(Medium) rs371911199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_857787,Human_Splice_Rec_857877 96035 RMVar_ID_96035 Human_SNP_ID_316844662 m1A Human chr7 + 36396389 36396389 36396389 CTAAGCGAGCTAGACAGCCACTTTCAGAAGCAAGTAACCAGCAGCCCCTCTCTGGTGGTGAAGGT CTAAGCGAGCTAGACAGCCACTTTCAGAAGCAGGTAACCAGCAGCCCCTCTCTGGTGGTGAAGGT A G ANLN Ensembl:ENSG00000011426 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:36396251..36396425 32194978 MeRIP-seq:(Medium) rs761254343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26357697 Human_Splice_Rec_857883,Human_Splice_Rec_857927,Human_Splice_Rec_857973 RMVar_hsa_circ_69728,RMVar_hsa_circ_365588 96036 RMVar_ID_96036 Human_SNP_ID_316848908 m1A Human chr7 + 36414124 36414124 36414124 TCTACTGGGTTTTGAAGCAAGAAGTTTGCTGTAACGTGGCAAGAGCAGTGTTAGTGAAGAGGTGA TCTACTGGGTTTTGAAGCAAGAAGTTTGCTGTCACGTGGCAAGAGCAGTGTTAGTGAAGAGGTGA A C ANLN Ensembl:ENSG00000011426 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:36414100..36414436 26863196 MeRIP-seq:(Medium) rs1428956813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99060,RMVar_hsa_circ_21737,RMVar_hsa_circ_344871,RMVar_hsa_circ_322638,RMVar_hsa_circ_273491,RMVar_hsa_circ_119375,RMVar_hsa_circ_104991,RMVar_hsa_circ_244642,RMVar_hsa_circ_244641,RMVar_hsa_circ_122113,RMVar_hsa_circ_244644,RMVar_hsa_circ_108155,RMVar_hsa_circ_111988,RMVar_hsa_circ_76781,RMVar_hsa_circ_244648,RMVar_hsa_circ_244652,RMVar_hsa_circ_84457,RMVar_hsa_circ_92065,RMVar_hsa_circ_77002,RMVar_hsa_circ_244653,RMVar_hsa_circ_244650,RMVar_hsa_circ_244651,RMVar_hsa_circ_244649,RMVar_hsa_circ_244646,RMVar_hsa_circ_244647,RMVar_hsa_circ_357347,RMVar_hsa_circ_35290,RMVar_hsa_circ_244655,RMVar_hsa_circ_74064,RMVar_hsa_circ_347171 96037 RMVar_ID_96037 Human_SNP_ID_316855389 m1A Human chr7 + 36440608 36440608 36440608 TGTTAAGATGGGAGAGACGTAAGCGGCTTTAAATGTAGATGGGTAGCTTCTAATAGGGCCAAAGA TGTTAAGATGGGAGAGACGTAAGCGGCTTTAAGTGTAGATGGGTAGCTTCTAATAGGGCCAAAGA A G ANLN Ensembl:ENSG00000011426 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:36440558..36440668 26863196 MeRIP-seq:(Medium) rs1265399637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10352296,Human_RBP_ID_16148091 RMVar_hsa_circ_122113,RMVar_hsa_circ_111988,RMVar_hsa_circ_244652,RMVar_hsa_circ_244653,RMVar_hsa_circ_336842,RMVar_hsa_circ_244656,RMVar_hsa_circ_20522,RMVar_hsa_circ_309686,RMVar_hsa_circ_359489 96038 RMVar_ID_96038 Human_SNP_ID_317211073 m1A Human chr7 - 37920722 37920722 37920722 CCGGGACCAGGGCCCGGGGAAGGCTCCAGTGAATCGCGCGGGAGCTATTTCTGCCTGGGCCACTG CCGGGACCAGGGCCCGGGGAAGGCTCCAGTGATTCGCGCGGGAGCTATTTCTGCCTGGGCCACTG T A SFRP4 Ensembl:ENSG00000106483 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:37920671..37920805 26863196 MeRIP-seq:(Medium) rs759405824 Functional Loss SNV dbSNP153 33..33 33 - - - 96039 RMVar_ID_96039 Human_SNP_ID_317283876 m1A Human chr7 + 38207553 38207553 38207553 AAGACATGGAGAACGCTCTCACCGGGAGCCAGAGCTCCCATGCTTCTCTGCGCAATATCCATTCC AAGACATGGAGAACGCTCTCACCGGGAGCCAGCGCTCCCATGCTTCTCTGCGCAATATCCATTCC A C STARD3NL Ensembl:ENSG00000010270 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:38207504..38207605 32194978 MeRIP-seq:(Medium) rs1406901141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956279 Human_miRNA_ID_2082942 RMVar_hsa_circ_7760,RMVar_hsa_circ_291431,RMVar_hsa_circ_17579,RMVar_hsa_circ_29336,RMVar_hsa_circ_341508,RMVar_hsa_circ_344642,RMVar_hsa_circ_301869,RMVar_hsa_circ_244696,RMVar_hsa_circ_277880 96040 RMVar_ID_96040 Human_SNP_ID_317323313 m1A Human chr7 + 38353246 38353246 38353246 GGTGTTTCAGTGGTCATTATAGTATTGCTTACATTGTTATAGATATAAGGAATAAGCACCAGTCT GGTGTTTCAGTGGTCATTATAGTATTGCTTACGTTGTTATAGATATAAGGAATAAGCACCAGTCT A G TRG-AS1 Ensembl:ENSG00000281103 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:38353198..38353285 26863410 MeRIP-seq:(Medium) rs991118779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22528729 96041 RMVar_ID_96041 Human_SNP_ID_317391792 m1A Human chr7 + 38631390 38631390 38631390 GGGTCCGGGGAGCTGCGAAGAGCAGAGCGCGCAGCGGGGCTGGCGGCGGCGCGGAGGAGCGGGAG GGGTCCGGGGAGCTGCGAAGAGCAGAGCGCGCGGCGGGGCTGGCGGCGGCGCGGAGGAGCGGGAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:38631303..38631408 26863410 MeRIP-seq:(Medium) rs1347670492 Functional Loss SNV dbSNP153 33..33 33 - - - 96042 RMVar_ID_96042 Human_SNP_ID_317422664 m1A Human chr7 - 38761181 38761181 38761181 GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGACAAGGAAGGAAAGACAAGGAAAGGGAAACAGA GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGTCAAGGAAGGAAAGACAAGGAAAGGGAAACAGA T A VPS41 Ensembl:ENSG00000006715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:38761132..38761234 26863196 MeRIP-seq:(Medium) rs2286084 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12613,GWAS_ID_12614,GWAS_ID_12615,GWAS_ID_12616,GWAS_ID_12617,GWAS_ID_12618,GWAS_ID_12619,GWAS_ID_12620,GWAS_ID_12621,GWAS_ID_12622,GWAS_ID_12623,GWAS_ID_12624 RMVar_hsa_circ_43146,RMVar_hsa_circ_68611,RMVar_hsa_circ_244709,RMVar_hsa_circ_111681,RMVar_hsa_circ_343704,RMVar_hsa_circ_363123,RMVar_hsa_circ_33766,RMVar_hsa_circ_33247,RMVar_hsa_circ_84413,RMVar_hsa_circ_50262,RMVar_hsa_circ_76428,RMVar_hsa_circ_244710,RMVar_hsa_circ_244711 96043 RMVar_ID_96043 Human_SNP_ID_317422665 m1A Human chr7 - 38761181 38761181 38761181 GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGACAAGGAAGGAAAGACAAGGAAAGGGAAACAGA GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGGCAAGGAAGGAAAGACAAGGAAAGGGAAACAGA T C VPS41 Ensembl:ENSG00000006715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:38761132..38761234 26863196 MeRIP-seq:(Medium) rs2286084 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12613,GWAS_ID_12614,GWAS_ID_12615,GWAS_ID_12616,GWAS_ID_12617,GWAS_ID_12618,GWAS_ID_12619,GWAS_ID_12620,GWAS_ID_12621,GWAS_ID_12622,GWAS_ID_12623,GWAS_ID_12624 RMVar_hsa_circ_43146,RMVar_hsa_circ_68611,RMVar_hsa_circ_244709,RMVar_hsa_circ_111681,RMVar_hsa_circ_343704,RMVar_hsa_circ_363123,RMVar_hsa_circ_33766,RMVar_hsa_circ_33247,RMVar_hsa_circ_84413,RMVar_hsa_circ_50262,RMVar_hsa_circ_76428,RMVar_hsa_circ_244710,RMVar_hsa_circ_244711 96044 RMVar_ID_96044 Human_SNP_ID_317429810 m1A Human chr7 + 38792816 38792816 38792816 CTGGGCTCCAACATCACCTGCTCCTCCACCACACCCTCCCCGACCCCCACTTACATCCCTCTCCT CTGGGCTCCAACATCACCTGCTCCTCCACCACCCCCTCCCCGACCCCCACTTACATCCCTCTCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:38792788..38792933 26863196 MeRIP-seq:(Medium) rs1454940061 Functional Loss SNV dbSNP153 33..33 33 - - - 96045 RMVar_ID_96045 Human_SNP_ID_317607773 m1A Human chr7 + 39566464 39566463 39566464 AAGCAGCCTCCTTGATCCAGGGCCCTGGAGACAAAGGGGACGTGTTTGACGAAGAAGCAGACGAG AAGCAGCCTCCTTGATCCAGGGCCCTGGAGAC_AAGGGGACGTGTTTGACGAAGAAGCAGACGAG CA C YAE1 Ensembl:ENSG00000241127 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:39566408..39566554 26863196 MeRIP-seq:(Medium) rs1373116425 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4940416 Human_Splice_Rec_859377,Human_Splice_Rec_859379,Human_Splice_Rec_859383,Human_Splice_Rec_859387 96046 RMVar_ID_96046 Human_SNP_ID_317607774 m1A Human chr7 + 39566464 39566464 39566464 AAGCAGCCTCCTTGATCCAGGGCCCTGGAGACAAAGGGGACGTGTTTGACGAAGAAGCAGACGAG AAGCAGCCTCCTTGATCCAGGGCCCTGGAGACCAAGGGGACGTGTTTGACGAAGAAGCAGACGAG A C YAE1 Ensembl:ENSG00000241127 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:39566408..39566554 26863196 MeRIP-seq:(Medium) rs1340549134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4940416 Human_Splice_Rec_859377,Human_Splice_Rec_859379,Human_Splice_Rec_859383,Human_Splice_Rec_859387 96047 RMVar_ID_96047 Human_SNP_ID_317620694 m1A Human chr7 - 39622169 39622169 39622169 TTGCTAGGGGCAGCTGCCAGATAGGAGAATGGAAGAGGCAATGATGATGCCTTGTTTTGCTTTGA TTGCTAGGGGCAGCTGCCAGATAGGAGAATGGTAGAGGCAATGATGATGCCTTGTTTTGCTTTGA T A AC004837.4 Ensembl:ENSG00000287584 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:39621988..39622328 26863196 MeRIP-seq:(Medium) rs1421575944 Functional Loss SNV dbSNP153 33..33 33 - - - 96048 RMVar_ID_96048 Human_SNP_ID_317621230 m1A Human chr7 - 39623815 39623815 39623815 GGCCCGAGCGGGCATCGCTCACCTGCACCGCGAGCCAGTCCGCCGCCCCGAGGGCTCCGGAAGCC GGCCCGAGCGGGCATCGCTCACCTGCACCGCGCGCCAGTCCGCCGCCCCGAGGGCTCCGGAAGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:39623680..39623890 32194978 MeRIP-seq:(Medium) rs1249778796 Functional Loss SNV dbSNP153 33..33 33 - - - 96049 RMVar_ID_96049 Human_SNP_ID_317636826 m1A Human chr7 + 39690411 39690411 39690411 TAGTTTGTGGAGGACTATGAGCCTACCAAAGCAGACAGCTATCGGAAGAAGGTAGTGCTAGATGG TAGTTTGTGGAGGACTATGAGCCTACCAAAGCTGACAGCTATCGGAAGAAGGTAGTGCTAGATGG A T RALA Ensembl:ENSG00000006451 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:39690377..39690497 26863196 MeRIP-seq:(Medium) rs1307161118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26130318 Human_Splice_Rec_859404,Human_Splice_Rec_859412,Human_Splice_Rec_859414 RMVar_hsa_circ_5019,RMVar_hsa_circ_98359,RMVar_hsa_circ_244729,RMVar_hsa_circ_76319,RMVar_hsa_circ_293839,RMVar_hsa_circ_344243,RMVar_hsa_circ_244730,RMVar_hsa_circ_244731,RMVar_hsa_circ_111550,RMVar_hsa_circ_244732 96050 RMVar_ID_96050 Human_SNP_ID_317669671 m1A Human chr7 - 39833304 39833292 39833304 CGGCTCGGCCTGGGGGTGCCGCCGCCGCCCGCACGGCCGCCCGCTCTCCGCTCGCTCGCGCGCCC CGGCTCGGCCTGGGGGTGCCGCCGCCGCCCGC____________TCTCCGCTCGCTCGCGCGCCC AGCGGGCGGCCGT A AC004987.1 Ensembl:ENSG00000231198 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:39833254..39833338 26863196 MeRIP-seq:(Medium) rs1242947324 Functional Loss DEL dbSNP153 33..44 33 - - - 96051 RMVar_ID_96051 Human_SNP_ID_317669767 m1A Human chr7 + 39833527 39833527 39833527 AGCGAGGAGCAGCGCGGGAGAGCCGGAGCGGTAGCGGCGGCGGCGGCGAGGCTCGGCGCCCTCTT AGCGAGGAGCAGCGCGGGAGAGCCGGAGCGGTGGCGGCGGCGGCGGCGAGGCTCGGCGCCCTCTT A G AC004987.2 Ensembl:ENSG00000237251 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:39833256..39833563 26863196 MeRIP-seq:(Medium) rs1420271013 Functional Loss SNV dbSNP153 33..33 33 - - - 96052 RMVar_ID_96052 Human_SNP_ID_317696853 m1A Human chr7 - 39949442 39949442 39949442 GGTGGGACTCCGTGTGAAGAAGGGTTAAAGAAAGGAGAGGATTCGTGTGCCGCCCACTGCTGTTG GGTGGGACTCCGTGTGAAGAAGGGTTAAAGAAGGGAGAGGATTCGTGTGCCGCCCACTGCTGTTG T C AC072061.1 Ensembl:ENSG00000259826 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:39949392..39949459 26863196 MeRIP-seq:(Medium) rs1277640231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5307458,Human_RBP_ID_5627597 96053 RMVar_ID_96053 Human_SNP_ID_317697060 m1A Human chr7 + 39949829 39949829 39949829 ACCAGGAGCCTCCTCGTGGAGGGGGGGAGCGGAGGAAAGGGGTAGCTCCGCCACCTCTGCTGGCG ACCAGGAGCCTCCTCGTGGAGGGGGGGAGCGGCGGAAAGGGGTAGCTCCGCCACCTCTGCTGGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:39949655..39950181 26863196 MeRIP-seq:(Medium) rs1013563661 Functional Loss SNV dbSNP153 33..33 33 - - - 96054 RMVar_ID_96054 Human_SNP_ID_317697121 m1A Human chr7 + 39949922 39949921 39949922 GTCAGGGCCCGTACCTACCGCCACAGACTCAGAAACGCCCCTGCCCCCATCTCCCCGGAAATAGC GTCAGGGCCCGTACCTACCGCCACAGACTCAG_AACGCCCCTGCCCCCATCTCCCCGGAAATAGC GA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:39949901..39950100 26863196 MeRIP-seq:(Medium) rs1301596481 Functional Loss DEL dbSNP153 33..33 33 - - - 96055 RMVar_ID_96055 Human_SNP_ID_317697154 m1A Human chr7 + 39949991 39949991 39949991 CGCCCAGCCCCGCACAGTCGCTGCCCCAACCGAGAGCCGCAGCCCGGTCGCCCCCGCCTCGCCCC CGCCCAGCCCCGCACAGTCGCTGCCCCAACCGGGAGCCGCAGCCCGGTCGCCCCCGCCTCGCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:39949730..39950236 26863196 MeRIP-seq:(Medium) rs1283050855 Functional Loss SNV dbSNP153 33..33 33 - - - 96056 RMVar_ID_96056 Human_SNP_ID_317697454 m1A Human chr7 - 39950705 39950705 39950705 CAGGAATCGCCTCCGCTTGCGGCGTTCCTCCAACTTCTTCTCCGCCCAGCTCAGGCCCCCGCCTC CAGGAATCGCCTCCGCTTGCGGCGTTCCTCCAGCTTCTTCTCCGCCCAGCTCAGGCCCCCGCCTC T C RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:39949715..39950800 26863196 MeRIP-seq:(Medium) rs775323128 Functional Loss SNV dbSNP153 33..33 33 - - - 96057 RMVar_ID_96057 Human_SNP_ID_317697462 m1A Human chr7 - 39950732 39950732 39950732 CAACAGCAGCGGCGGCTGCTGAGGGGACAGGAATCGCCTCCGCTTGCGGCGTTCCTCCAACTTCT CAACAGCAGCGGCGGCTGCTGAGGGGACAGGAGTCGCCTCCGCTTGCGGCGTTCCTCCAACTTCT T C RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:39950726..39950750 26863196 MeRIP-seq:(Medium) rs1340392766 Functional Loss SNV dbSNP153 33..33 33 - - - 96058 RMVar_ID_96058 Human_SNP_ID_317697756 m1A Human chr7 + 39951270 39951270 39951270 CCGGGACCGCCGCAGCAGCAGTGGCCGCAGCAAGGAGCGCCACCGCGAGCACCGGCGGCGGGATG CCGGGACCGCCGCAGCAGCAGTGGCCGCAGCAGGGAGCGCCACCGCGAGCACCGGCGGCGGGATG A G CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:39951151..39951375 26863196 MeRIP-seq:(Medium) rs971194567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 96059 RMVar_ID_96059 Human_SNP_ID_317697993 m1A Human chr7 + 39951650 39951650 39951650 CGGTGTCCCACAGGGCCTCTCAGAGCCTGAGGAGCCGCAAGTCCCCCAGCCCGGCAGGAGGTGGC CGGTGTCCCACAGGGCCTCTCAGAGCCTGAGGGGCCGCAAGTCCCCCAGCCCGGCAGGAGGTGGC A G CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:39951602..39951807 26863196 MeRIP-seq:(Medium) rs780906753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9311781 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 96060 RMVar_ID_96060 Human_SNP_ID_317698057 m1A Human chr7 + 39951746 39951745 39951746 CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCCAGCTACAGCCGCCACAGCTCCTACGAGCGGGGC CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCC_GCTACAGCCGCCACAGCTCCTACGAGCGGGGC CA C CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:39951604..39951792 26863196 MeRIP-seq:(Medium) rs1047357117 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9337116,Human_RBP_ID_17426934 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 96061 RMVar_ID_96061 Human_SNP_ID_317698059 m1A Human chr7 + 39951746 39951746 39951746 CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCCAGCTACAGCCGCCACAGCTCCTACGAGCGGGGC CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCCCGCTACAGCCGCCACAGCTCCTACGAGCGGGGC A C CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:39951604..39951792 26863196 MeRIP-seq:(Medium) rs1323247446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337116,Human_RBP_ID_17426934 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 96062 RMVar_ID_96062 Human_SNP_ID_317747063 m1A Human chr7 - 40134422 40134422 40134422 GCCCTCCCCTCGAGACGGGTACGGGAGTCCGCACCACACGCCGCCGTACGGGCCCCGGTCTAGGC GCCCTCCCCTCGAGACGGGTACGGGAGTCCGCGCCACACGCCGCCGTACGGGCCCCGGTCTAGGC T C MPLKIP Ensembl:ENSG00000168303 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:40134226..40134558 26863196 MeRIP-seq:(Medium) rs1180071223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18100140,Human_RBP_ID_22463049 96063 RMVar_ID_96063 Human_SNP_ID_317747159 m1A Human chr7 - 40134559 40134559 40134559 AGGTTTTCGGCTTTGGCTCCTGATATGCAGCGACAGAATTTTCGGCCCCCAACTCCTCCTTACCC AGGTTTTCGGCTTTGGCTCCTGATATGCAGCGGCAGAATTTTCGGCCCCCAACTCCTCCTTACCC T C MPLKIP Ensembl:ENSG00000168303 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:40134226..40134625 26863196 MeRIP-seq:(Medium) rs746398211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1686521,Human_RBP_ID_4956288,Human_RBP_ID_8667050,Human_RBP_ID_9337118,Human_RBP_ID_16153842,Human_RBP_ID_22112305,Human_RBP_ID_22323028,Human_RBP_ID_27113322 96064 RMVar_ID_96064 Human_SNP_ID_318219550 m1A Human chr7 + 42056060 42056060 42056060 CCTGCACGGGCTCTCTCCTCTTGTCTGCCACCATGTGAGAAGTGCCTTTCATCTTCCACCATGAT CCTGCACGGGCTCTCTCCTCTTGTCTGCCACCGTGTGAGAAGTGCCTTTCATCTTCCACCATGAT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:42056051..42056164 26863196 MeRIP-seq:(Medium) rs528208328 Functional Loss SNV dbSNP153 33..33 33 - - - 96065 RMVar_ID_96065 Human_SNP_ID_318263741 m1A Human chr7 - 42237557 42237557 42237557 AGCGCGGGGAGGAGGAGGAAGAGGAGGAGAGAAGGGAAGGAGGGAGCGCGCGGGAGGGGAGCGCG AGCGCGGGGAGGAGGAGGAAGAGGAGGAGAGAGGGGAAGGAGGGAGCGCGCGGGAGGGGAGCGCG T C GLI3 Ensembl:ENSG00000106571 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:42237529..42237601 26863196 MeRIP-seq:(Medium) rs914839961 Functional Loss SNV dbSNP153 33..33 33 - - - 96066 RMVar_ID_96066 Human_SNP_ID_318432486 m1A Human chr7 + 42927339 42927339 42927339 ATTAATTACTAATGAATTCCAAAATAATTAGGATAACTACTAACAGGCATCTGAAATGAATGAAG ATTAATTACTAATGAATTCCAAAATAATTAGGGTAACTACTAACAGGCATCTGAAATGAATGAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:42927335..42927411 26863196 MeRIP-seq:(Medium) rs770814567 Functional Loss SNV dbSNP153 33..33 33 - - - 96067 RMVar_ID_96067 Human_SNP_ID_318433730 m1A Human chr7 - 42932070 42932070 42932070 TCGAGGTCTTCAGCGTAGTCGAGGTTGCTGGTACTCTGTCGATTTAGTTTTTCCCATCCTGACGT TCGAGGTCTTCAGCGTAGTCGAGGTTGCTGGTTCTCTGTCGATTTAGTTTTTCCCATCCTGACGT T A PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:42932067..42932175 26863196 MeRIP-seq:(Medium) rs543303729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16155430 96068 RMVar_ID_96068 Human_SNP_ID_318433731 m1A Human chr7 - 42932070 42932070 42932070 TCGAGGTCTTCAGCGTAGTCGAGGTTGCTGGTACTCTGTCGATTTAGTTTTTCCCATCCTGACGT TCGAGGTCTTCAGCGTAGTCGAGGTTGCTGGTGCTCTGTCGATTTAGTTTTTCCCATCCTGACGT T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:42932067..42932175 26863196 MeRIP-seq:(Medium) rs543303729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16155430 96069 RMVar_ID_96069 Human_SNP_ID_318433919 m1A Human chr7 - 42932409 42932409 42932409 CTCCCCGGGCCGCAGACCACGGCGAAACCACCAAGACCAGCATGGCCAGCGCCATTTTCCCTGCT CTCCCCGGGCCGCAGACCACGGCGAAACCACCGAGACCAGCATGGCCAGCGCCATTTTCCCTGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:42932351..42932450 26863196 MeRIP-seq:(Medium) rs1189688118 Functional Loss SNV dbSNP153 33..33 33 - - - 96070 RMVar_ID_96070 Human_SNP_ID_318551918 m1A Human chr7 + 43444649 43444649 43444649 CCAAGGAGGAGCCCTTGGAGGAGGAAGCAACGACCCAGAGCCGGGCTGGAAGGGAAGAAGAGGAG CCAAGGAGGAGCCCTTGGAGGAGGAAGCAACGTCCCAGAGCCGGGCTGGAAGGGAAGAAGAGGAG A T HECW1 Ensembl:ENSG00000002746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43444546..43444763 26863196 MeRIP-seq:(Medium) rs774986986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14274,RMVar_hsa_circ_114790,RMVar_hsa_circ_244810,RMVar_hsa_circ_41784 96071 RMVar_ID_96071 Human_SNP_ID_318556953 m1A Human chr7 + 43466104 43466101 43466105 AAGGAAGGAGAGAGAAGAAAGAGAAAGAAGGAAAGAAAGATGAAAGAAAGAAAAAGAAAGAAAGG AAGGAAGGAGAGAGAAGAAAGAGAAAGAAG____GAAAGATGAAAGAAAGAAAAAGAAAGAAAGG GGAAA G HECW1 Ensembl:ENSG00000002746 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43466091..43466233 26863196 MeRIP-seq:(Medium) rs1356768412 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_14274,RMVar_hsa_circ_114790,RMVar_hsa_circ_244810,RMVar_hsa_circ_244833,RMVar_hsa_circ_244815,RMVar_hsa_circ_11290,RMVar_hsa_circ_284663,RMVar_hsa_circ_41784,RMVar_hsa_circ_335035,RMVar_hsa_circ_342093,RMVar_hsa_circ_321022,RMVar_hsa_circ_323182,RMVar_hsa_circ_309316,RMVar_hsa_circ_18488,RMVar_hsa_circ_35022,RMVar_hsa_circ_16053,RMVar_hsa_circ_244819,RMVar_hsa_circ_244821,RMVar_hsa_circ_244823,RMVar_hsa_circ_244822,RMVar_hsa_circ_244820,RMVar_hsa_circ_244817,RMVar_hsa_circ_244818,RMVar_hsa_circ_244816,RMVar_hsa_circ_244826,RMVar_hsa_circ_244830,RMVar_hsa_circ_305941,RMVar_hsa_circ_323061,RMVar_hsa_circ_331921,RMVar_hsa_circ_349710,RMVar_hsa_circ_314275,RMVar_hsa_circ_304179,RMVar_hsa_circ_23217,RMVar_hsa_circ_270113,RMVar_hsa_circ_244831,RMVar_hsa_circ_244828,RMVar_hsa_circ_244829,RMVar_hsa_circ_244827,RMVar_hsa_circ_244837,RMVar_hsa_circ_293803,RMVar_hsa_circ_317286,RMVar_hsa_circ_332893,RMVar_hsa_circ_323036,RMVar_hsa_circ_314729,RMVar_hsa_circ_282652,RMVar_hsa_circ_283066,RMVar_hsa_circ_244838,RMVar_hsa_circ_244835,RMVar_hsa_circ_244836,RMVar_hsa_circ_244834,RMVar_hsa_circ_244832 96072 RMVar_ID_96072 Human_SNP_ID_318576086 m1A Human chr7 + 43550542 43550542 43550542 GTACATCGAGCGCATGGTGAAGTGGCGGGTGGAGCGCGGCGTGGTACAGCAGACCGAGGCGCTGG GTACATCGAGCGCATGGTGAAGTGGCGGGTGGGGCGCGGCGTGGTACAGCAGACCGAGGCGCTGG A G HECW1 Ensembl:ENSG00000002746 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:43550497..43550582;chr7:43550491..43550597 26863196 MeRIP-seq:(Medium) rs76552943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_860344,Human_Splice_Rec_860345,Human_Splice_Rec_860402,Human_Splice_Rec_860403 RMVar_hsa_circ_18488,RMVar_hsa_circ_23217,RMVar_hsa_circ_2193 96073 RMVar_ID_96073 Human_SNP_ID_318583360 m1A Human chr7 - 43583198 43583198 43583198 GCTTCTTTCCTGGCCGCCTGTTCACTCCGAGCAGCCGGAGGGTCACGGACCCGCCCCCGGCTCCT GCTTCTTTCCTGGCCGCCTGTTCACTCCGAGCGGCCGGAGGGTCACGGACCCGCCCCCGGCTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43583151..43583229 26863196 MeRIP-seq:(Medium) rs1207302315 Functional Loss SNV dbSNP153 33..33 33 - - - 96074 RMVar_ID_96074 Human_SNP_ID_318586454 m1A Human chr7 - 43595953 43595953 43595953 TTTTCTTCTTTTTCTCATGAACTTTGCAGCAAATTCTTTCCCAGAATCTTTCTTTATACATTTTC TTTTCTTCTTTTTCTCATGAACTTTGCAGCAATTTCTTTCCCAGAATCTTTCTTTATACATTTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43595854..43595973 26863196 MeRIP-seq:(Medium) rs909666267 Functional Loss SNV dbSNP153 33..33 33 - - - 96075 RMVar_ID_96075 Human_SNP_ID_318610180 m1A Human chr7 - 43693151 43693151 43693151 ACACCTGCCCTGTCTCCAGGCCTGCTGGGAAGAGGGATGTAAGAGAGAAGACAGCTGTGGCTGAA ACACCTGCCCTGTCTCCAGGCCTGCTGGGAAGGGGGATGTAAGAGAGAAGACAGCTGTGGCTGAA T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43693148..43693753 26863196 MeRIP-seq:(Medium) rs1172203659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3089382,Human_RBP_ID_23076794 96076 RMVar_ID_96076 Human_SNP_ID_318610492 m1A Human chr7 + 43694617 43694617 43694617 AGACACACCACTCACTCTTGGTTCTCCTCCTTATTGAGCAATTCTTTTCCATCTCTGTTATTGGT AGACACACCACTCACTCTTGGTTCTCCTCCTTGTTGAGCAATTCTTTTCCATCTCTGTTATTGGT A G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43694612..43694703 26863196 MeRIP-seq:(Medium) rs961629828 Functional Loss SNV dbSNP153 33..33 33 - - - 96077 RMVar_ID_96077 Human_SNP_ID_318613803 m1A Human chr7 - 43708608 43708608 43708608 CAAGTGGCCAGTAAAAATAAGAAAAGGTGCCAAAGAGCACAAATCATTAGAGAAATGCAGATTAA CAAGTGGCCAGTAAAAATAAGAAAAGGTGCCAGAGAGCACAAATCATTAGAGAAATGCAGATTAA T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43708605..43708868 26863196 MeRIP-seq:(Medium) rs1253490491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22622826 96078 RMVar_ID_96078 Human_SNP_ID_318613820 m1A Human chr7 - 43708692 43708692 43708692 AGAATAATGGGTAAGAGAGAAAAAGACAAGCCAGTAGAATAATGGGTAAGAGACTTGAACAGGCA AGAATAATGGGTAAGAGAGAAAAAGACAAGCCCGTAGAATAATGGGTAAGAGACTTGAACAGGCA T G COA1 Ensembl:ENSG00000106603 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43708690..43708774 26863196 MeRIP-seq:(Medium) rs1164179800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16157942,Human_RBP_ID_22528771 96079 RMVar_ID_96079 Human_SNP_ID_318619037 m1A Human chr7 + 43729396 43729395 43729396 AATTGCAGGAACAAACGCTTCTTGCTGGGGGGAAGACGGAGACTCTTATACCGCGGGAGACTAAC AATTGCAGGAACAAACGCTTCTTGCTGGGGGG_AGACGGAGACTCTTATACCGCGGGAGACTAAC GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43729390..43729461 26863196 MeRIP-seq:(Medium) rs1368819387 Functional Loss DEL dbSNP153 33..33 33 - - - 96080 RMVar_ID_96080 Human_SNP_ID_318619039 m1A Human chr7 + 43729396 43729396 43729396 AATTGCAGGAACAAACGCTTCTTGCTGGGGGGAAGACGGAGACTCTTATACCGCGGGAGACTAAC AATTGCAGGAACAAACGCTTCTTGCTGGGGGGTAGACGGAGACTCTTATACCGCGGGAGACTAAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43729390..43729461 26863196 MeRIP-seq:(Medium) rs1046235227 Functional Loss SNV dbSNP153 33..33 33 - - - 96081 RMVar_ID_96081 Human_SNP_ID_318625807 m1A Human chr7 - 43758736 43758736 43758736 TGCGCGCGACCCCCGTTCCCCGCGCGCGCCTCACCTGACGCGGGCACCGCTCTCCGTGCAGCCTC TGCGCGCGACCCCCGTTCCCCGCGCGCGCCTCTCCTGACGCGGGCACCGCTCTCCGTGCAGCCTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:43758676..43758796;chr7:43758724..43758810;chr7:43758676..43758878;chr7:43758676..43758893;chr7:43758676..43758813 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1238245171 Functional Loss SNV dbSNP153 33..33 33 - - - 96082 RMVar_ID_96082 Human_SNP_ID_318632319 m1A Human chr7 + 43787858 43787858 43787858 GCCAGCTCCTTTGTTTTGTAGTTTTCTGCTCGATGCCTACAGTGTTTTCAGACTCCACCTTGGTC GCCAGCTCCTTTGTTTTGTAGTTTTCTGCTCGGTGCCTACAGTGTTTTCAGACTCCACCTTGGTC A G BLVRA Ensembl:ENSG00000106605 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:43787852..43787965 26863196 MeRIP-seq:(Medium) rs953752957 Functional Loss SNV dbSNP153 33..33 33 - - - 96083 RMVar_ID_96083 Human_SNP_ID_318632320 m1A Human chr7 + 43787858 43787858 43787858 GCCAGCTCCTTTGTTTTGTAGTTTTCTGCTCGATGCCTACAGTGTTTTCAGACTCCACCTTGGTC GCCAGCTCCTTTGTTTTGTAGTTTTCTGCTCGTTGCCTACAGTGTTTTCAGACTCCACCTTGGTC A T BLVRA Ensembl:ENSG00000106605 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:43787852..43787965 26863196 MeRIP-seq:(Medium) rs953752957 Functional Loss SNV dbSNP153 33..33 33 - - - 96084 RMVar_ID_96084 Human_SNP_ID_318632352 m1A Human chr7 - 43787936 43787936 43787936 TCCCTCATCCGCACGGAGCCGGCTCGGCCAACACCAACCACCACCACGCCAAACTTCCTCTCGGG TCCCTCATCCGCACGGAGCCGGCTCGGCCAACGCCAACCACCACCACGCCAAACTTCCTCTCGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43771096..43788050 26863196 MeRIP-seq:(Medium) rs775346802 Functional Loss SNV dbSNP153 33..33 33 - - - 96085 RMVar_ID_96085 Human_SNP_ID_318633487 m1A Human chr7 - 43792771 43792771 43792771 CAGCCAGCTCCCACAGTTCCTGAGCGGCCGCCAATGACAGTGTCATGGGGTATTCCACAAGGACG CAGCCAGCTCCCACAGTTCCTGAGCGGCCGCCGATGACAGTGTCATGGGGTATTCCACAAGGACG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:43792726..43800421 32194978 MeRIP-seq:(Medium) rs148571710 Functional Loss SNV dbSNP153 33..33 33 - - - 96086 RMVar_ID_96086 Human_SNP_ID_318636614 m1A Human chr7 - 43807097 43807097 43807097 AGTTTCTGGACAAATATATTTTGATCTTTCAGAAATATGTTCTTATTCACTCCTACATTTGGCAC AGTTTCTGGACAAATATATTTTGATCTTTCAGGAATATGTTCTTATTCACTCCTACATTTGGCAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:43807046..43807145 32194978 MeRIP-seq:(Medium) rs1332313031 Functional Loss SNV dbSNP153 33..33 33 - - - 96087 RMVar_ID_96087 Human_SNP_ID_318650413 m1A Human chr7 - 43866784 43866784 43866784 ACACAAGTACTACTTCCTCGTGGGCTACAGTGAAACTTTGCTGTCCTACTTTTACAAATGTCCTG ACACAAGTACTACTTCCTCGTGGGCTACAGTGTAACTTTGCTGTCCTACTTTTACAAATGTCCTG T A URGCP-MRPS24,MRPS24 Ensembl:ENSG00000270617,Ensembl:ENSG00000062582 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:43866606..43869400 32194978 MeRIP-seq:(Medium) rs536686794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684383,Human_RBP_ID_1052067,Human_RBP_ID_1398822,Human_RBP_ID_1686671,Human_RBP_ID_2043025,Human_RBP_ID_3846998,Human_RBP_ID_5122730,Human_RBP_ID_5452401,Human_RBP_ID_8667391,Human_RBP_ID_9211233,Human_RBP_ID_17312927,Human_RBP_ID_17665270,Human_RBP_ID_18100538,Human_RBP_ID_24216050 Human_miRNA_ID_2881792,Human_miRNA_ID_2881793 RMVar_hsa_circ_96225,RMVar_hsa_circ_108232,RMVar_hsa_circ_125975,RMVar_hsa_circ_103610,RMVar_hsa_circ_244865,RMVar_hsa_circ_244867,RMVar_hsa_circ_244869,RMVar_hsa_circ_95866,RMVar_hsa_circ_244868,RMVar_hsa_circ_244866 96088 RMVar_ID_96088 Human_SNP_ID_318650504 m1A Human chr7 - 43866980 43866980 43866980 GATTCTTCTATTATGCCCTTCCCTCTTCAGGTAACCTGGATGGAGAGGACCATGCCGCAGAGCGA GATTCTTCTATTATGCCCTTCCCTCTTCAGGTTACCTGGATGGAGAGGACCATGCCGCAGAGCGA T A URGCP-MRPS24,MRPS24 Ensembl:ENSG00000270617,Ensembl:ENSG00000062582 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:43866954..43869449 32194978 MeRIP-seq:(Medium) rs1165861130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956468,Human_RBP_ID_4957116,Human_RBP_ID_18100540,Human_RBP_ID_22463467,Human_RBP_ID_22686802,Human_RBP_ID_23140073 Human_Splice_Rec_860704,Human_Splice_Rec_860708,Human_Splice_Rec_860710,Human_Splice_Rec_860716,Human_Splice_Rec_860730 Human_miRNA_ID_2570439,Human_miRNA_ID_2570440 RMVar_hsa_circ_96225,RMVar_hsa_circ_108232,RMVar_hsa_circ_125975,RMVar_hsa_circ_103610,RMVar_hsa_circ_244865,RMVar_hsa_circ_244867,RMVar_hsa_circ_244869,RMVar_hsa_circ_95866,RMVar_hsa_circ_244868,RMVar_hsa_circ_244866 96089 RMVar_ID_96089 Human_SNP_ID_318650505 m1A Human chr7 - 43866980 43866980 43866980 GATTCTTCTATTATGCCCTTCCCTCTTCAGGTAACCTGGATGGAGAGGACCATGCCGCAGAGCGA GATTCTTCTATTATGCCCTTCCCTCTTCAGGTGACCTGGATGGAGAGGACCATGCCGCAGAGCGA T C URGCP-MRPS24,MRPS24 Ensembl:ENSG00000270617,Ensembl:ENSG00000062582 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:43866954..43869449 32194978 MeRIP-seq:(Medium) rs1165861130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956468,Human_RBP_ID_4957116,Human_RBP_ID_18100540,Human_RBP_ID_22463467,Human_RBP_ID_22686802,Human_RBP_ID_23140073 Human_Splice_Rec_860704,Human_Splice_Rec_860708,Human_Splice_Rec_860710,Human_Splice_Rec_860716,Human_Splice_Rec_860730 Human_miRNA_ID_2570439,Human_miRNA_ID_2570440 RMVar_hsa_circ_96225,RMVar_hsa_circ_108232,RMVar_hsa_circ_125975,RMVar_hsa_circ_103610,RMVar_hsa_circ_244865,RMVar_hsa_circ_244867,RMVar_hsa_circ_244869,RMVar_hsa_circ_95866,RMVar_hsa_circ_244868,RMVar_hsa_circ_244866 96090 RMVar_ID_96090 Human_SNP_ID_318653349 m1A Human chr7 + 43877976 43877976 43877976 CTTGGGCTGCCTTTCTCCAGGGGTCCCCCTGCAGCCTCAGCTCGTCCCTTCTGTAGGCATCCGAG CTTGGGCTGCCTTTCTCCAGGGGTCCCCCTGCCGCCTCAGCTCGTCCCTTCTGTAGGCATCCGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43877928..43878090 26863196 MeRIP-seq:(Medium) rs1311577089 Functional Loss SNV dbSNP153 33..33 33 - - - 96091 RMVar_ID_96091 Human_SNP_ID_318656271 m1A Human chr7 + 43889690 43889690 43889690 CTCCTCTTAATCTACTCCCATTGCTCTAGCCCATTCTGTTAACAGATAGAAGAGTAGTGCTTTCG CTCCTCTTAATCTACTCCCATTGCTCTAGCCCGTTCTGTTAACAGATAGAAGAGTAGTGCTTTCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43889685..43889808 26863196 MeRIP-seq:(Medium) rs1049926463 Functional Loss SNV dbSNP153 33..33 33 - - - 96092 RMVar_ID_96092 Human_SNP_ID_318659280 m1A Human chr7 + 43902330 43902327 43902331 CCCAATTAGCCACACATTCCTGGGTTTCAATCACTCAGTCACCTCATCCACTACCATGAGTCCCA CCCAATTAGCCACACATTCCTGGGTTTCAA____TCAGTCACCTCATCCACTACCATGAGTCCCA ATCAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:43902324..43902419 26863196 MeRIP-seq:(Medium) rs10579045 Functional Loss DEL dbSNP153 31..34 33 - - - GWAS_ID_12625,GWAS_ID_12626,GWAS_ID_12627,GWAS_ID_12628,GWAS_ID_12629,GWAS_ID_12630,GWAS_ID_12631,GWAS_ID_12632,GWAS_ID_12633,GWAS_ID_12634,GWAS_ID_12635,GWAS_ID_12636,GWAS_ID_12637,GWAS_ID_12638,GWAS_ID_12639,GWAS_ID_12640,GWAS_ID_12641,GWAS_ID_12642,GWAS_ID_12643,GWAS_ID_12644,GWAS_ID_12645,GWAS_ID_12646,GWAS_ID_12647,GWAS_ID_12648,GWAS_ID_12649,GWAS_ID_12650,GWAS_ID_12651,GWAS_ID_12652,GWAS_ID_12653,GWAS_ID_12654,GWAS_ID_12655,GWAS_ID_12656,GWAS_ID_12657 96093 RMVar_ID_96093 Human_SNP_ID_318663286 m1A Human chr7 + 43919441 43919441 43919441 GGCCAGCACCATCACCCTGCGCTACCCCAGCTACATGGACAATGACCTCATAGGCCTCATCGCCT GGCCAGCACCATCACCCTGCGCTACCCCAGCTGCATGGACAATGACCTCATAGGCCTCATCGCCT A G TUBG1P Ensembl:ENSG00000237972 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43919390..43919461 26863196 MeRIP-seq:(Medium) rs540448953 Functional Loss SNV dbSNP153 33..33 33 - - - 96094 RMVar_ID_96094 Human_SNP_ID_318664084 m1A Human chr7 - 43922955 43922952 43922956 GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGAGAGAAAGAGAGAAGGAAAGAAAGAAAGAAAGACG GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGA____AAGAGAGAAGGAAAGAAAGAAAGAAAGACG TTCTC T URGCP Ensembl:ENSG00000106608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43922798..43922999 26863196 MeRIP-seq:(Medium) rs955767377 Functional Loss DEL dbSNP153 32..35 33 - - - 96095 RMVar_ID_96095 Human_SNP_ID_318664085 m1A Human chr7 - 43922955 43922952 43922956 GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGAGAGAAAGAGAGAAGGAAAGAAAGAAAGAAAGACG GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGA__GAAAGAGAGAAGGAAAGAAAGAAAGAAAGACG TTCTC TTC URGCP Ensembl:ENSG00000106608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43922798..43922999 26863196 MeRIP-seq:(Medium) rs955767377 Functional Loss DEL dbSNP153 32..33 33 - - - 96096 RMVar_ID_96096 Human_SNP_ID_318664087 m1A Human chr7 - 43922955 43922955 43922955 GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGAGAGAAAGAGAGAAGGAAAGAAAGAAAGAAAGACG GAAAGTAAGAGAGAGAGAGAGGAGAAAGAGAGCGAAAGAGAGAAGGAAAGAAAGAAAGAAAGACG T G URGCP Ensembl:ENSG00000106608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43922798..43922999 26863196 MeRIP-seq:(Medium) rs556280128 Functional Loss SNV dbSNP153 33..33 33 - - - 96097 RMVar_ID_96097 Human_SNP_ID_318677204 m1A Human chr7 - 43977653 43977650 43977654 GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAGAAAGGAAGGAAGGAAGGAGGGAAGGGAAGGAAAG GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAG____GAAGGAAGGAAGGAGGGAAGGGAAGGAAAG CCTTT C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43977603..43977857 26863196 MeRIP-seq:(Medium) rs1324921953 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96098 RMVar_ID_96098 Human_SNP_ID_318677205 m1A Human chr7 - 43977653 43977651 43977653 GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAGAAAGGAAGGAAGGAAGGAGGGAAGGGAAGGAAAG GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAGA__GGAAGGAAGGAAGGAGGGAAGGGAAGGAAAG CTT C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43977603..43977857 26863196 MeRIP-seq:(Medium) rs1355950283 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96099 RMVar_ID_96099 Human_SNP_ID_318677208 m1A Human chr7 - 43977653 43977653 43977653 GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAGAAAGGAAGGAAGGAAGGAGGGAAGGGAAGGAAAG GGGGAAGGAAGGAGGGGAAGGAAGGAGAGAGAGAGGAAGGAAGGAAGGAGGGAAGGGAAGGAAAG T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:43977603..43977857 26863196 MeRIP-seq:(Medium) rs1304343862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96100 RMVar_ID_96100 Human_SNP_ID_318677308 m1A Human chr7 - 43977810 43977806 43977810 AGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAGAAGGAAGGAAAGAAA AGAGAGAGAGAGAGAGAAAGATGAAAGAAAGA____GAAAGCAAAGAAAGAAGGAAGGAAAGAAA CTTTT C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:43977513..43977922 26863196 MeRIP-seq:(Medium) rs373513708 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23081665 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96101 RMVar_ID_96101 Human_SNP_ID_318677309 m1A Human chr7 - 43977810 43977806 43977810 AGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAGAAGGAAGGAAAGAAA AGAGAGAGAGAGAGAGAAAGATGAAAGAAAGA_AAAGAAAGCAAAGAAAGAAGGAAGGAAAGAAA CTTTT CTTT POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:43977513..43977922 26863196 MeRIP-seq:(Medium) rs373513708 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23081665 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96102 RMVar_ID_96102 Human_SNP_ID_318677311 m1A Human chr7 - 43977819 43977813 43977820 AAGAAAGGGAGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAGAAGGAA AAGAAAGGGAGAGAGAGAGAGAGAGAAAGAT_______AGAAAAAGAAAGCAAAGAAAGAAGGAA TTTCTTTC T POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:43977503..43977908 26863196 MeRIP-seq:(Medium) rs1261921165 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_23081665 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96103 RMVar_ID_96103 Human_SNP_ID_318679108 m1A Human chr7 - 43984966 43984966 43984966 CTGAGGGGTACCAGAGGGGCCCACGTGTCCCTACACCTCCTCCCTGGCCCAGGCTGCAGAGCCTG CTGAGGGGTACCAGAGGGGCCCACGTGTCCCTCCACCTCCTCCCTGGCCCAGGCTGCAGAGCCTG T G POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:43984957..43985060 26863196 MeRIP-seq:(Medium) rs62458704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624377 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_16703,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787,RMVar_hsa_circ_297953,RMVar_hsa_circ_327104,RMVar_hsa_circ_107215,RMVar_hsa_circ_244883 96104 RMVar_ID_96104 Human_SNP_ID_318684978 m1A Human chr7 + 44005172 44005172 44005172 AGTATCTCCTTGCTATGGTCATAGCGTATTTCAGCCGAGCCGGCTTCCCCTCCTGGCAATACCAA AGTATCTCCTTGCTATGGTCATAGCGTATTTCGGCCGAGCCGGCTTCCCCTCCTGGCAATACCAA A G SPDYE1 Ensembl:ENSG00000136206 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44005121..44005212;chr7:44005110..44005212 26863196 MeRIP-seq:(Medium) rs753017820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_861012,Human_Splice_Rec_861013,Human_Splice_Rec_861024,Human_Splice_Rec_861025 96105 RMVar_ID_96105 Human_SNP_ID_318685264 m1A Human chr7 + 44006234 44006234 44006234 GTGTTTGTGTTTTCTGTCTGGGTGTCCCGCATACATGTGGCTCTGAAGGGAAGGACCCATTCCTT GTGTTTGTGTTTTCTGTCTGGGTGTCCCGCATCCATGTGGCTCTGAAGGGAAGGACCCATTCCTT A C SPDYE1 Ensembl:ENSG00000136206 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44006204..44006280 26863196 MeRIP-seq:(Medium) rs546134415 Functional Loss SNV dbSNP153 33..33 33 - - - 96106 RMVar_ID_96106 Human_SNP_ID_318688572 m1A Human chr7 + 44019102 44019102 44019102 CCCTCGAAGAGCAAGAACGACTCGAAGGCTGGAGGGGCGTTCACGCTCCCGCCTCCGTTGCGTCC CCCTCGAAGAGCAAGAACGACTCGAAGGCTGGTGGGGCGTTCACGCTCCCGCCTCCGTTGCGTCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44016436..44019121 26863410 MeRIP-seq:(Medium) rs942962637 Functional Loss SNV dbSNP153 33..33 33 - - - 96107 RMVar_ID_96107 Human_SNP_ID_318688598 m1A Human chr7 - 44019132 44019132 44019132 GGTGGCGGCGGCGGCAGACACTTGGGGTCTGGACGCAACGGAGGCGGGAGCGTGAACGCCCCTCC GGTGGCGGCGGCGGCAGACACTTGGGGTCTGGTCGCAACGGAGGCGGGAGCGTGAACGCCCCTCC T A AC017116.2,POLR2J4,POLR2J4:2,AC004951.4 Ensembl:ENSG00000285596,Ensembl:ENSG00000214783,Ensembl:ENSG00000272655,Ensembl:ENSG00000273432 lincRNA,lincRNA,Pseudogene,lincRNA intron,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44019007..44019175 26863196 MeRIP-seq:(Medium) rs1014617742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1052084,Human_RBP_ID_4956316,Human_RBP_ID_5104679,Human_RBP_ID_5269971,Human_RBP_ID_5623310,Human_RBP_ID_18425993 Human_Splice_Rec_860925,Human_Splice_Rec_860955,Human_Splice_Rec_860971,Human_Splice_Rec_861045,Human_Splice_Rec_861049 RMVar_hsa_circ_125501,RMVar_hsa_circ_244894,RMVar_hsa_circ_80248,RMVar_hsa_circ_244896 96108 RMVar_ID_96108 Human_SNP_ID_318688599 m1A Human chr7 - 44019132 44019132 44019132 GGTGGCGGCGGCGGCAGACACTTGGGGTCTGGACGCAACGGAGGCGGGAGCGTGAACGCCCCTCC GGTGGCGGCGGCGGCAGACACTTGGGGTCTGGGCGCAACGGAGGCGGGAGCGTGAACGCCCCTCC T C AC017116.2,POLR2J4,POLR2J4:2,AC004951.4 Ensembl:ENSG00000285596,Ensembl:ENSG00000214783,Ensembl:ENSG00000272655,Ensembl:ENSG00000273432 lincRNA,lincRNA,Pseudogene,lincRNA intron,exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44019007..44019175 26863196 MeRIP-seq:(Medium) rs1014617742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1052084,Human_RBP_ID_4956316,Human_RBP_ID_5104679,Human_RBP_ID_5269971,Human_RBP_ID_5623310,Human_RBP_ID_18425993 Human_Splice_Rec_860925,Human_Splice_Rec_860955,Human_Splice_Rec_860971,Human_Splice_Rec_861045,Human_Splice_Rec_861049 RMVar_hsa_circ_125501,RMVar_hsa_circ_244894,RMVar_hsa_circ_80248,RMVar_hsa_circ_244896 96109 RMVar_ID_96109 Human_SNP_ID_318695846 m1A Human chr7 + 44044759 44044759 44044759 CGGGGCGGGCCATGGCGGCGAACCTGAGCCGGAACGGGCCAGCGCTGCAAGAGGCCTACGTGCGG CGGGGCGGGCCATGGCGGCGAACCTGAGCCGGCACGGGCCAGCGCTGCAAGAGGCCTACGTGCGG A C DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44044713..44044979 26863196 MeRIP-seq:(Medium) rs1357443015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794274,Human_RBP_ID_4956317,Human_RBP_ID_18425994,Human_RBP_ID_19020686 Human_Splice_Rec_861093,Human_Splice_Rec_861115,Human_Splice_Rec_861133,Human_Splice_Rec_861153,Human_Splice_Rec_861163,Human_Splice_Rec_861165,Human_Splice_Rec_861183,Human_Splice_Rec_861201,Human_Splice_Rec_861213,Human_Splice_Rec_861243,Human_Splice_Rec_861263,Human_Splice_Rec_861271,Human_Splice_Rec_861291,Human_Splice_Rec_861329,Human_Splice_Rec_861351,Human_Splice_Rec_861369 96110 RMVar_ID_96110 Human_SNP_ID_318695848 m1A Human chr7 + 44044767 44044767 44044767 GCCATGGCGGCGAACCTGAGCCGGAACGGGCCAGCGCTGCAAGAGGCCTACGTGCGGGTGGTCAC GCCATGGCGGCGAACCTGAGCCGGAACGGGCCGGCGCTGCAAGAGGCCTACGTGCGGGTGGTCAC A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:44044676..44044907;chr7:44044676..44045010;chr7:44044676..44049907 26863196 MeRIP-seq:(Medium) rs1280804314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794274,Human_RBP_ID_4956318,Human_RBP_ID_8667450,Human_RBP_ID_18425994,Human_RBP_ID_19020686 Human_Splice_Rec_861093,Human_Splice_Rec_861115,Human_Splice_Rec_861133,Human_Splice_Rec_861153,Human_Splice_Rec_861163,Human_Splice_Rec_861165,Human_Splice_Rec_861183,Human_Splice_Rec_861201,Human_Splice_Rec_861213,Human_Splice_Rec_861221,Human_Splice_Rec_861243,Human_Splice_Rec_861263,Human_Splice_Rec_861271,Human_Splice_Rec_861291,Human_Splice_Rec_861313,Human_Splice_Rec_861329,Human_Splice_Rec_861351,Human_Splice_Rec_861369 96111 RMVar_ID_96111 Human_SNP_ID_318695854 m1A Human chr7 + 44044775 44044775 44044775 GGCGAACCTGAGCCGGAACGGGCCAGCGCTGCAAGAGGCCTACGTGCGGGTGGTCACCGAGAAGT GGCGAACCTGAGCCGGAACGGGCCAGCGCTGCGAGAGGCCTACGTGCGGGTGGTCACCGAGAAGT A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:44044676..44044850 26863410 MeRIP-seq:(Medium) rs1196137990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794274,Human_RBP_ID_4956318,Human_RBP_ID_8667450,Human_RBP_ID_18425994,Human_RBP_ID_19020686 Human_Splice_Rec_861093,Human_Splice_Rec_861115,Human_Splice_Rec_861133,Human_Splice_Rec_861153,Human_Splice_Rec_861163,Human_Splice_Rec_861165,Human_Splice_Rec_861183,Human_Splice_Rec_861201,Human_Splice_Rec_861213,Human_Splice_Rec_861221,Human_Splice_Rec_861243,Human_Splice_Rec_861263,Human_Splice_Rec_861271,Human_Splice_Rec_861291,Human_Splice_Rec_861313,Human_Splice_Rec_861329,Human_Splice_Rec_861351,Human_Splice_Rec_861369 96112 RMVar_ID_96112 Human_SNP_ID_318695869 m1A Human chr7 - 44044822 44044822 44044822 CCCTGGCCCGACCCTGGCCCGTCTCGCCGCCCACCAGTCGGTCGGGGACTTCTCGGTGACCACCC CCCTGGCCCGACCCTGGCCCGTCTCGCCGCCCCCCAGTCGGTCGGGGACTTCTCGGTGACCACCC T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:44044726..44044850 26863410 MeRIP-seq:(Medium) rs113430237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244898 96113 RMVar_ID_96113 Human_SNP_ID_318697114 m1A Human chr7 + 44050274 44050274 44050274 AAGGCAACAGCAATGACATCCGCGTGGCTGGCACAGGGGGTGAGTATGACTCCAAATGGACTCAG AAGGCAACAGCAATGACATCCGCGTGGCTGGCGCAGGGGGTGAGTATGACTCCAAATGGACTCAG A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:44050170..44050329;chr7:44050138..44050300;chr7:44050176..44050334;chr7:44050169..44050340;chr7:44050156..44050300 26863196 MeRIP-seq:(Medium) rs1460667328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843582,Human_RBP_ID_16159460,Human_RBP_ID_24216152 Human_Splice_Rec_861094,Human_Splice_Rec_861095,Human_Splice_Rec_861116,Human_Splice_Rec_861117,Human_Splice_Rec_861134,Human_Splice_Rec_861135,Human_Splice_Rec_861164,Human_Splice_Rec_861184,Human_Splice_Rec_861202,Human_Splice_Rec_861203,Human_Splice_Rec_861222,Human_Splice_Rec_861223,Human_Splice_Rec_861244,Human_Splice_Rec_861245,Human_Splice_Rec_861264,Human_Splice_Rec_861265,Human_Splice_Rec_861272,Human_Splice_Rec_861273,Human_Splice_Rec_861292,Human_Splice_Rec_861293,Human_Splice_Rec_861314,Human_Splice_Rec_861315,Human_Splice_Rec_861330,Human_Splice_Rec_861331,Human_Splice_Rec_861352,Human_Splice_Rec_861353,Human_Splice_Rec_861370,Human_Splice_Rec_861371,Human_Splice_Rec_861395 Human_miRNA_ID_2397293 RMVar_hsa_circ_244901,RMVar_hsa_circ_310885,RMVar_hsa_circ_334262,RMVar_hsa_circ_334923,RMVar_hsa_circ_367546,RMVar_hsa_circ_311762,RMVar_hsa_circ_8823,RMVar_hsa_circ_244900 96114 RMVar_ID_96114 Human_SNP_ID_318699015 m1A Human chr7 + 44058175 44058175 44058175 CCGTCGGCTGGAGGAAAAGCGGCGGGCCGAGGAGGCACAGCGGCAGCTGGAGCAGGAGCGCCGGG CCGTCGGCTGGAGGAAAAGCGGCGGGCCGAGGCGGCACAGCGGCAGCTGGAGCAGGAGCGCCGGG A C DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44058073..44058312 26863196 MeRIP-seq:(Medium) rs774552738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843587,Human_RBP_ID_953133,Human_RBP_ID_19019547,Human_RBP_ID_23080643 Human_Splice_Rec_861104,Human_Splice_Rec_861122,Human_Splice_Rec_861142,Human_Splice_Rec_861172,Human_Splice_Rec_861190,Human_Splice_Rec_861212,Human_Splice_Rec_861218,Human_Splice_Rec_861232,Human_Splice_Rec_861252,Human_Splice_Rec_861270,Human_Splice_Rec_861280,Human_Splice_Rec_861302,Human_Splice_Rec_861322,Human_Splice_Rec_861340,Human_Splice_Rec_861358,Human_Splice_Rec_861402,Human_Splice_Rec_861418 RMVar_hsa_circ_85672,RMVar_hsa_circ_334923,RMVar_hsa_circ_8823,RMVar_hsa_circ_39116,RMVar_hsa_circ_244902,RMVar_hsa_circ_264961,RMVar_hsa_circ_85183,RMVar_hsa_circ_244905 96115 RMVar_ID_96115 Human_SNP_ID_318699059 m1A Human chr7 + 44058250 44058250 44058250 GCGTGAGGCTGCACGCCGGGAGCAGCGCTATCAGGAGCAGGGTGGCGAGGCCAGCCCCCAGAGGT GCGTGAGGCTGCACGCCGGGAGCAGCGCTATCGGGAGCAGGGTGGCGAGGCCAGCCCCCAGAGGT A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:44058043..44058508;chr7:44058076..44058500 26863196 MeRIP-seq:(Medium) rs1278325084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253500,Human_RBP_ID_9403338,Human_RBP_ID_19019548,Human_RBP_ID_23080643,Human_RBP_ID_26357733 Human_Splice_Rec_861105,Human_Splice_Rec_861123,Human_Splice_Rec_861143,Human_Splice_Rec_861173,Human_Splice_Rec_861191,Human_Splice_Rec_861219,Human_Splice_Rec_861233,Human_Splice_Rec_861253,Human_Splice_Rec_861281,Human_Splice_Rec_861303,Human_Splice_Rec_861323,Human_Splice_Rec_861341,Human_Splice_Rec_861359,Human_Splice_Rec_861385,Human_Splice_Rec_861403,Human_Splice_Rec_861419 RMVar_hsa_circ_85672,RMVar_hsa_circ_334923,RMVar_hsa_circ_8823,RMVar_hsa_circ_39116,RMVar_hsa_circ_244902,RMVar_hsa_circ_264961,RMVar_hsa_circ_85183,RMVar_hsa_circ_244905 96116 RMVar_ID_96116 Human_SNP_ID_318699060 m1A Human chr7 + 44058250 44058250 44058250 GCGTGAGGCTGCACGCCGGGAGCAGCGCTATCAGGAGCAGGGTGGCGAGGCCAGCCCCCAGAGGT GCGTGAGGCTGCACGCCGGGAGCAGCGCTATCTGGAGCAGGGTGGCGAGGCCAGCCCCCAGAGGT A T DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:44058043..44058508;chr7:44058076..44058500 26863196 MeRIP-seq:(Medium) rs1278325084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253500,Human_RBP_ID_9403338,Human_RBP_ID_19019548,Human_RBP_ID_23080643,Human_RBP_ID_26357733 Human_Splice_Rec_861105,Human_Splice_Rec_861123,Human_Splice_Rec_861143,Human_Splice_Rec_861173,Human_Splice_Rec_861191,Human_Splice_Rec_861219,Human_Splice_Rec_861233,Human_Splice_Rec_861253,Human_Splice_Rec_861281,Human_Splice_Rec_861303,Human_Splice_Rec_861323,Human_Splice_Rec_861341,Human_Splice_Rec_861359,Human_Splice_Rec_861385,Human_Splice_Rec_861403,Human_Splice_Rec_861419 RMVar_hsa_circ_85672,RMVar_hsa_circ_334923,RMVar_hsa_circ_8823,RMVar_hsa_circ_39116,RMVar_hsa_circ_244902,RMVar_hsa_circ_264961,RMVar_hsa_circ_85183,RMVar_hsa_circ_244905 96117 RMVar_ID_96117 Human_SNP_ID_318699140 m1A Human chr7 + 44058463 44058463 44058463 GGACGTGGGAGCAGCAGCAAGAAGTGGTTTCAAGGAACCGAAATGAGCAGGTAAGATGGGGGTGC GGACGTGGGAGCAGCAGCAAGAAGTGGTTTCAGGGAACCGAAATGAGCAGGTAAGATGGGGGTGC A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44058143..44058500 32194978 MeRIP-seq:(Medium) rs752906605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3847091,Human_RBP_ID_19020697 Human_Splice_Rec_861106,Human_Splice_Rec_861107,Human_Splice_Rec_861124,Human_Splice_Rec_861125,Human_Splice_Rec_861144,Human_Splice_Rec_861145,Human_Splice_Rec_861174,Human_Splice_Rec_861175,Human_Splice_Rec_861192,Human_Splice_Rec_861193,Human_Splice_Rec_861220,Human_Splice_Rec_861234,Human_Splice_Rec_861235,Human_Splice_Rec_861254,Human_Splice_Rec_861255,Human_Splice_Rec_861282,Human_Splice_Rec_861283,Human_Splice_Rec_861304,Human_Splice_Rec_861305,Human_Splice_Rec_861324,Human_Splice_Rec_861325,Human_Splice_Rec_861342,Human_Splice_Rec_861343,Human_Splice_Rec_861360,Human_Splice_Rec_861361,Human_Splice_Rec_861386,Human_Splice_Rec_861387,Human_Splice_Rec_861404,Human_Splice_Rec_861405,Human_Splice_Rec_861420 RMVar_hsa_circ_85672,RMVar_hsa_circ_334923,RMVar_hsa_circ_8823,RMVar_hsa_circ_39116,RMVar_hsa_circ_244902,RMVar_hsa_circ_85183,RMVar_hsa_circ_244905 96118 RMVar_ID_96118 Human_SNP_ID_318699263 m1A Human chr7 - 44058912 44058912 44058912 TCTCCTTCTGCTTGAAAATCTCCCTCGGGTGCACGGCAGACTCCTGGAGGGAAGCACATGTTGAC TCTCCTTCTGCTTGAAAATCTCCCTCGGGTGCGCGGCAGACTCCTGGAGGGAAGCACATGTTGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44058901..44058975;chr7:44058901..44059000 26863196 MeRIP-seq:(Medium) rs1233782532 Functional Loss SNV dbSNP153 33..33 33 - - - 96119 RMVar_ID_96119 Human_SNP_ID_318699405 m1A Human chr7 + 44059357 44059357 44059357 GTGATGTATATATTTACCCGGGTTTGCAGGCAAGCTGAGGAGCCCCTTCCTGCAGAAGCAGCTCA GTGATGTATATATTTACCCGGGTTTGCAGGCAGGCTGAGGAGCCCCTTCCTGCAGAAGCAGCTCA A G DBNL Ensembl:ENSG00000136279 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44059351..44059450 26863196 MeRIP-seq:(Medium) rs1468267635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954342,Human_RBP_ID_19020700 Human_Splice_Rec_861110,Human_Splice_Rec_861128,Human_Splice_Rec_861148,Human_Splice_Rec_861178,Human_Splice_Rec_861196,Human_Splice_Rec_861238,Human_Splice_Rec_861258,Human_Splice_Rec_861286,Human_Splice_Rec_861308,Human_Splice_Rec_861328,Human_Splice_Rec_861346,Human_Splice_Rec_861364,Human_Splice_Rec_861390,Human_Splice_Rec_861408,Human_Splice_Rec_861422 RMVar_hsa_circ_334923,RMVar_hsa_circ_8823,RMVar_hsa_circ_43520,RMVar_hsa_circ_85183,RMVar_hsa_circ_244905 96120 RMVar_ID_96120 Human_SNP_ID_318700367 m1A Human chr7 - 44062913 44062913 44062913 TTCCTTCCGGCATAGGGATGTCAGACCAGGCGATCATGGAGCTGAACCTGCCCACGGGGATCCCC TTCCTTCCGGCATAGGGATGTCAGACCAGGCGTTCATGGAGCTGAACCTGCCCACGGGGATCCCC T A PGAM2 Ensembl:ENSG00000164708 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44062862..44062963 32194978 MeRIP-seq:(Medium) rs754757980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_861436 RMVar_hsa_circ_121048,RMVar_hsa_circ_244908,RMVar_hsa_circ_117225,RMVar_hsa_circ_244907 96121 RMVar_ID_96121 Human_SNP_ID_318701646 m1A Human chr7 + 44067093 44067093 44067093 GGACCATAATGTACTGGGAGAGATGGGAAAGGAGAGGCCGGGGACAGCCCTGAGGTGACATGTGA GGACCATAATGTACTGGGAGAGATGGGAAAGGGGAGGCCGGGGACAGCCCTGAGGTGACATGTGA A G DBNL Ensembl:ENSG00000136279 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44067051..44067258 26863196 MeRIP-seq:(Medium) rs1410125365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254330,Human_RBP_ID_794277 96122 RMVar_ID_96122 Human_SNP_ID_318702922 m1A Human chr7 + 44072506 44072506 44072506 GGAGTTGGCCACAAGGGGGCCTGGGTGCATCAAATAGGAAGCCGGTGAGTCAAGCAGCTCGGGGC GGAGTTGGCCACAAGGGGGCCTGGGTGCATCAGATAGGAAGCCGGTGAGTCAAGCAGCTCGGGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44072456..44072531 26863196 MeRIP-seq:(Medium) rs1442623644 Functional Loss SNV dbSNP153 33..33 33 - - - 96123 RMVar_ID_96123 Human_SNP_ID_318705955 m1A Human chr7 - 44082429 44082429 44082429 CGCTGCTGGAGGCTGTCGTCCCAATGCTCCCCAAACGGCGGCGAGCGCGGGTCGGGTCCCCTAGC CGCTGCTGGAGGCTGTCGTCCCAATGCTCCCCTAACGGCGGCGAGCGCGGGTCGGGTCCCCTAGC T A POLM Ensembl:ENSG00000122678 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44082381..44082472 26863196 MeRIP-seq:(Medium) rs1224498979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244909,RMVar_hsa_circ_100387 96124 RMVar_ID_96124 Human_SNP_ID_318705979 m1A Human chr7 + 44082465 44082465 44082465 GAGCATTGGGACGACAGCCTCCAGCAGCGCGGAGCGAACGCAGAGGGAAACTCCGAGCGAGACGG GAGCATTGGGACGACAGCCTCCAGCAGCGCGGGGCGAACGCAGAGGGAAACTCCGAGCGAGACGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:44082335..44082500;chr7:44082334..44082500 26863196 MeRIP-seq:(Medium) rs1412527754 Functional Loss SNV dbSNP153 33..33 33 - - - 96125 RMVar_ID_96125 Human_SNP_ID_318712843 m1A Human chr7 - 44109343 44109343 44109343 CCCCCACCCTCACCCCCTTGTGCCCCCCACTTACTGACTTTCTCCGTAGGCGTCCACTCCTCCTC CCCCCACCCTCACCCCCTTGTGCCCCCCACTTCCTGACTTTCTCCGTAGGCGTCCACTCCTCCTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44106601..44109695 32194978 MeRIP-seq:(Medium) rs112233452 Functional Loss SNV dbSNP153 33..33 33 - - - 96126 RMVar_ID_96126 Human_SNP_ID_318715105 m1A Human chr7 - 44115345 44115345 44115345 AACTGACCCGTTCATCTTCCCAGAGTGCCCGCATGTCTACTTTTGTGGCAACACCCCCAGCTTTG AACTGACCCGTTCATCTTCCCAGAGTGCCCGCGTGTCTACTTTTGTGGCAACACCCCCAGCTTTG T C POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44115275..44115415 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_684469,Human_RBP_ID_4963412,Human_RBP_ID_9403339,Human_RBP_ID_17665279,Human_RBP_ID_18882967,Human_RBP_ID_22774327 Human_Splice_Rec_861740,Human_Splice_Rec_861741,Human_Splice_Rec_861762,Human_Splice_Rec_861763,Human_Splice_Rec_861765,Human_Splice_Rec_861782,Human_Splice_Rec_861783,Human_Splice_Rec_861802,Human_Splice_Rec_861803 Human_miRNA_ID_2584976 RMVar_hsa_circ_122099,RMVar_hsa_circ_244917 96127 RMVar_ID_96127 Human_SNP_ID_318715333 m1A Human chr7 - 44116246 44116246 44116246 TTCCAGGCCTCAGTGCCCGTGGACGTGATGCCAGGCGAGTTTGATCCCACCAATTACACGCTCCC TTCCAGGCCTCAGTGCCCGTGGACGTGATGCCTGGCGAGTTTGATCCCACCAATTACACGCTCCC T A POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:44116118..44116289 26863196 MeRIP-seq:(Medium) rs1013887517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_861736,Human_Splice_Rec_861758,Human_Splice_Rec_861778,Human_Splice_Rec_861798,Human_Splice_Rec_861818 Human_miRNA_ID_1705728 RMVar_hsa_circ_122099,RMVar_hsa_circ_86638,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_244919 96128 RMVar_ID_96128 Human_SNP_ID_318715596 m1A Human chr7 - 44116923 44116923 44116923 CACCCAGCTGCTGGTGGATGTGGTGACGGGGCAGCTTGGGGACGAAGGGGAGCAGTGCAGCGCCG CACCCAGCTGCTGGTGGATGTGGTGACGGGGCTGCTTGGGGACGAAGGGGAGCAGTGCAGCGCCG T A POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:44116877..44116990 26863196 MeRIP-seq:(Medium) rs768827150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253252,Human_RBP_ID_793207,Human_RBP_ID_7740662,Human_RBP_ID_8910994,Human_RBP_ID_18100641,Human_RBP_ID_18882971,Human_RBP_ID_23140077,Human_RBP_ID_26356427 Human_Splice_Rec_861732,Human_Splice_Rec_861754,Human_Splice_Rec_861774,Human_Splice_Rec_861794,Human_Splice_Rec_861814,Human_Splice_Rec_861820,Human_Splice_Rec_861830 Human_miRNA_ID_2151009,Human_miRNA_ID_2240932,Human_miRNA_ID_2419495 RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_102487,RMVar_hsa_circ_244920 96129 RMVar_ID_96129 Human_SNP_ID_318715633 m1A Human chr7 + 44117012 44117011 44117012 CCACCCAGGCCCAGGCCGGACACCAGTAGCACAAACCTGCGGGAGAAGGTGGGGTCCTCCAGGGT CCACCCAGGCCCAGGCCGGACACCAGTAGCAC_AACCTGCGGGAGAAGGTGGGGTCCTCCAGGGT CA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44116976..44117025 26863196 MeRIP-seq:(Medium) rs1222908888 Functional Loss DEL dbSNP153 33..33 33 - - - 96130 RMVar_ID_96130 Human_SNP_ID_318715678 m1A Human chr7 - 44117147 44117147 44117147 GCTGACCTTGCTCCCCAGAAGCCCGCACCCCCACTTGACACAGATAGGTGAGCAGCAGTTCTCGG GCTGACCTTGCTCCCCAGAAGCCCGCACCCCCCCTTGACACAGATAGGTGAGCAGCAGTTCTCGG T G POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:44116793..44117147 26863196 MeRIP-seq:(Medium) rs756458946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684479,Human_RBP_ID_3971925,Human_RBP_ID_4941523,Human_RBP_ID_9211267,Human_RBP_ID_19019555,Human_RBP_ID_22110748 Human_Splice_Rec_861731,Human_Splice_Rec_861753,Human_Splice_Rec_861773,Human_Splice_Rec_861793,Human_Splice_Rec_861813,Human_Splice_Rec_861819,Human_Splice_Rec_861829 RMVar_hsa_circ_26723,RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_102487,RMVar_hsa_circ_244920 96131 RMVar_ID_96131 Human_SNP_ID_318715728 m1A Human chr7 - 44117249 44117249 44117249 CTCCCTGCTCAGGCCTGATGCCACTGCTCCCCAGGGACTGTCCTGGCTGTGTTTGGCTCCGTGAG CTCCCTGCTCAGGCCTGATGCCACTGCTCCCCTGGGACTGTCCTGGCTGTGTTTGGCTCCGTGAG T A POLD2 Ensembl:ENSG00000106628 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44117201..44117250 32194978 MeRIP-seq:(Medium) rs112735840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956123,Human_RBP_ID_4941531,Human_RBP_ID_19134791,Human_RBP_ID_22554656,Human_RBP_ID_22685377 RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_102487,RMVar_hsa_circ_244920 96132 RMVar_ID_96132 Human_SNP_ID_318715729 m1A Human chr7 - 44117249 44117249 44117249 CTCCCTGCTCAGGCCTGATGCCACTGCTCCCCAGGGACTGTCCTGGCTGTGTTTGGCTCCGTGAG CTCCCTGCTCAGGCCTGATGCCACTGCTCCCCGGGGACTGTCCTGGCTGTGTTTGGCTCCGTGAG T C POLD2 Ensembl:ENSG00000106628 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44117201..44117250 32194978 MeRIP-seq:(Medium) rs112735840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956123,Human_RBP_ID_4941531,Human_RBP_ID_19134791,Human_RBP_ID_22554656,Human_RBP_ID_22685377 RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_102487,RMVar_hsa_circ_244920 96133 RMVar_ID_96133 Human_SNP_ID_318715881 m1A Human chr7 - 44117726 44117726 44117726 TGTCTCTGCATTCCAGCACAACCTGCTCCCCCAGCCTCCTCGGAGTAAATACATACACCCAGATG TGTCTCTGCATTCCAGCACAACCTGCTCCCCCGGCCTCCTCGGAGTAAATACATACACCCAGATG T C POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:44117676..44117750 32194978 MeRIP-seq:(Medium) rs775485254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793210,Human_RBP_ID_3971927,Human_RBP_ID_8910998,Human_RBP_ID_26830330 Human_Splice_Rec_861728,Human_Splice_Rec_861750,Human_Splice_Rec_861770,Human_Splice_Rec_861790,Human_Splice_Rec_861826,Human_Splice_Rec_861834,Human_Splice_Rec_861842,Human_Splice_Rec_861846,Human_Splice_Rec_861850,Human_Splice_Rec_861852,Human_Splice_Rec_861858,Human_Splice_Rec_861864 Human_miRNA_ID_2088745,Human_miRNA_ID_2089622,Human_miRNA_ID_2683859,Human_miRNA_ID_2713612,Human_miRNA_ID_3049590 RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918,RMVar_hsa_circ_102487,RMVar_hsa_circ_244920,RMVar_hsa_circ_106283,RMVar_hsa_circ_126276,RMVar_hsa_circ_244921,RMVar_hsa_circ_244922 96134 RMVar_ID_96134 Human_SNP_ID_318716951 m1A Human chr7 - 44122070 44122070 44122070 CCTTGGCCTGGGCGAAGCTGTGTGGACCAAGCAAGTCAGGAGTGTGGCCATGTTTTCTGAGCAGG CCTTGGCCTGGGCGAAGCTGTGTGGACCAAGCGAGTCAGGAGTGTGGCCATGTTTTCTGAGCAGG T C POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:44122026..44122150 26863410 MeRIP-seq:(Medium) rs751699655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953136,Human_RBP_ID_1686813,Human_RBP_ID_3847137,Human_RBP_ID_4941554,Human_RBP_ID_8667529,Human_RBP_ID_8911002,Human_RBP_ID_17312945,Human_RBP_ID_22463958,Human_RBP_ID_27161566 Human_Splice_Rec_861724,Human_Splice_Rec_861810,Human_Splice_Rec_861822,Human_Splice_Rec_861838,Human_Splice_Rec_861854,Human_Splice_Rec_861860,Human_Splice_Rec_861866,Human_Splice_Rec_861872 RMVar_hsa_circ_126276,RMVar_hsa_circ_244922 96135 RMVar_ID_96135 Human_SNP_ID_318736801 m1A Human chr7 - 44201009 44201009 44201009 CGGCCTCTCAGCAGCCGGCTGCTGACGGGGCCACCGCCGGCTTCCTCCTCCTGGCTCGCAATCCA CGGCCTCTCAGCAGCCGGCTGCTGACGGGGCCGCCGCCGGCTTCCTCCTCCTGGCTCGCAATCCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44200995..44201224 26863196 MeRIP-seq:(Medium) rs559441435 Functional Loss SNV dbSNP153 33..33 33 - - - 96136 RMVar_ID_96136 Human_SNP_ID_318736829 m1A Human chr7 - 44201032 44201032 44201032 CCCTCGGGACCGCCGCCGCCTACCGGCCTCTCAGCAGCCGGCTGCTGACGGGGCCACCGCCGGCT CCCTCGGGACCGCCGCCGCCTACCGGCCTCTCGGCAGCCGGCTGCTGACGGGGCCACCGCCGGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44200976..44201225;chr7:44200976..44201250 26863196 MeRIP-seq:(Medium) rs1355989319 Functional Loss SNV dbSNP153 33..33 33 - - - 96137 RMVar_ID_96137 Human_SNP_ID_318736875 m1A Human chr7 + 44201101 44201101 44201101 CGGCCGCGCTGCTCCCTGAGAACGGGTCCCGCAGCTGGGCAGGCGGGCGGCCTGAGGGCGCGGAG CGGCCGCGCTGCTCCCTGAGAACGGGTCCCGCTGCTGGGCAGGCGGGCGGCCTGAGGGCGCGGAG A T YKT6 Ensembl:ENSG00000106636 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44201001..44201225 26863410 MeRIP-seq:(Medium) rs780415522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794680,Human_RBP_ID_4941585,Human_RBP_ID_5328424 96138 RMVar_ID_96138 Human_SNP_ID_318739594 m1A Human chr7 + 44212326 44212326 44212326 AGAGGCCCAATGCTGGAATGGCACCATCATTCACATCAGAACTGCAGCCCCTGGAAAAGAAGAGA AGAGGCCCAATGCTGGAATGGCACCATCATTCGCATCAGAACTGCAGCCCCTGGAAAAGAAGAGA A G YKT6 Ensembl:ENSG00000106636 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44212276..44212488 26863196 MeRIP-seq:(Medium) rs776611788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2043162,Human_RBP_ID_8667546,Human_RBP_ID_16160309,Human_RBP_ID_17312951,Human_RBP_ID_17425514,Human_RBP_ID_18882996,Human_RBP_ID_26546799,Human_RBP_ID_27357612 Human_Splice_Rec_862102,Human_Splice_Rec_862114,Human_Splice_Rec_862128,Human_Splice_Rec_862140,Human_Splice_Rec_862142 RMVar_hsa_circ_113965,RMVar_hsa_circ_244924,RMVar_hsa_circ_103139,RMVar_hsa_circ_244928 96139 RMVar_ID_96139 Human_SNP_ID_318739600 m1A Human chr7 + 44212364 44212364 44212364 GAACTGCAGCCCCTGGAAAAGAAGAGACAGCCATAGACGAGGAGCCAGAGTGGGGGCAGACTGGC GAACTGCAGCCCCTGGAAAAGAAGAGACAGCCGTAGACGAGGAGCCAGAGTGGGGGCAGACTGGC A G YKT6 Ensembl:ENSG00000106636 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:44212313..44212455 26863196 MeRIP-seq:(Medium) rs924655039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7740724,Human_RBP_ID_16160312,Human_RBP_ID_17314549,Human_RBP_ID_17426935,Human_RBP_ID_24216283,Human_RBP_ID_26546800 Human_miRNA_ID_259464,Human_miRNA_ID_263259,Human_miRNA_ID_2082944,Human_miRNA_ID_2783714 RMVar_hsa_circ_113965,RMVar_hsa_circ_244924,RMVar_hsa_circ_103139,RMVar_hsa_circ_244928 96140 RMVar_ID_96140 Human_SNP_ID_318739603 m1A Human chr7 - 44212382 44212382 44212382 AACTTCAAAATAAAAATGGCCAGTCTGCCCCCACTCTGGCTCCTCGTCTATGGCTGTCTCTTCTT AACTTCAAAATAAAAATGGCCAGTCTGCCCCCGCTCTGGCTCCTCGTCTATGGCTGTCTCTTCTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44212376..44212400 26863196 MeRIP-seq:(Medium) rs1266624845 Functional Loss SNV dbSNP153 33..33 33 - - - 96141 RMVar_ID_96141 Human_SNP_ID_318739760 m1A Human chr7 - 44213007 44213007 44213007 GGGCTCAGTTCCTAGTCTACTTGCTGGTACGAACCCAACCCACACACTCCCCGCCCACAATGCAG GGGCTCAGTTCCTAGTCTACTTGCTGGTACGATCCCAACCCACACACTCCCCGCCCACAATGCAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44212859..44213081 26863196 MeRIP-seq:(Medium) rs139575583 Functional Loss SNV dbSNP153 33..33 33 - - - 96142 RMVar_ID_96142 Human_SNP_ID_318739761 m1A Human chr7 - 44213007 44213007 44213007 GGGCTCAGTTCCTAGTCTACTTGCTGGTACGAACCCAACCCACACACTCCCCGCCCACAATGCAG GGGCTCAGTTCCTAGTCTACTTGCTGGTACGAGCCCAACCCACACACTCCCCGCCCACAATGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44212859..44213081 26863196 MeRIP-seq:(Medium) rs139575583 Functional Loss SNV dbSNP153 33..33 33 - - - 96143 RMVar_ID_96143 Human_SNP_ID_318782581 m1A Human chr7 - 44384773 44384773 44384773 GTGCCCATCGCCGGGAGTATGGTTCAGCTGCCACCGGCACTGTCCATTTGCCTGTCTGTCAAGCT GTGCCCATCGCCGGGAGTATGGTTCAGCTGCCTCCGGCACTGTCCATTTGCCTGTCTGTCAAGCT T A NUDCD3 Ensembl:ENSG00000015676 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44384699..44385049 32194978 MeRIP-seq:(Medium) rs1302394765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27113807 Human_miRNA_ID_2515735 RMVar_hsa_circ_123718,RMVar_hsa_circ_244935 96144 RMVar_ID_96144 Human_SNP_ID_318784386 m1A Human chr7 + 44392395 44392395 44392395 CGCCTGTTCCTCCTCATCCACGGTGGCCATGGAGCGCTCCTTGTTGATCTTGTCAATGTCGATGG CGCCTGTTCCTCCTCATCCACGGTGGCCATGGTGCGCTCCTTGTTGATCTTGTCAATGTCGATGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44392347..44392441 26863196 MeRIP-seq:(Medium) rs369527166 Functional Loss SNV dbSNP153 33..33 33 - - - 96145 RMVar_ID_96145 Human_SNP_ID_318796736 m1A Human chr7 - 44444871 44444871 44444871 GGAAGAAACTGACTCAAGATGTTTCGCTGGGAATAAAAGGAAGAAGGCAGCAGCCTGAACAGAAG GGAAGAAACTGACTCAAGATGTTTCGCTGGGAGTAAAAGGAAGAAGGCAGCAGCCTGAACAGAAG T C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:44444859..44445168 26863196 MeRIP-seq:(Medium) rs1042777734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95003,RMVar_hsa_circ_244938,RMVar_hsa_circ_353272,RMVar_hsa_circ_101442,RMVar_hsa_circ_105601,RMVar_hsa_circ_244943,RMVar_hsa_circ_244948,RMVar_hsa_circ_244947 96146 RMVar_ID_96146 Human_SNP_ID_318802172 m1A Human chr7 + 44467961 44467961 44467961 GATCGTCAAAAAGAGAACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGC GATCGTCAAAAAGAGAACCAAGAAGTTCATCCGGCACCAGTCAGACCAATATGTCAAAATTAAGC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs562719193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1822365 96147 RMVar_ID_96147 Human_SNP_ID_318807669 m1A Human chr7 - 44490530 44490530 44490530 TTTGGGCATCCTGCAGCACGTGGGCAACGTCCAGGATTTCCTGCGCGTTCTCTTTGGCTTCCTCT TTTGGGCATCCTGCAGCACGTGGGCAACGTCCGGGATTTCCTGCGCGTTCTCTTTGGCTTCCTCT T C NUDCD3 Ensembl:ENSG00000015676 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44490480..44490581 32194978 MeRIP-seq:(Medium) rs752317758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_286200,Human_RBP_ID_1686908,Human_RBP_ID_2043302,Human_RBP_ID_9211336,Human_RBP_ID_18883121,Human_RBP_ID_19019561,Human_RBP_ID_22110751,Human_RBP_ID_26357737 Human_miRNA_ID_2508959,Human_miRNA_ID_2853235 RMVar_hsa_circ_95003,RMVar_hsa_circ_244938 96148 RMVar_ID_96148 Human_SNP_ID_318827832 m1A Human chr7 - 44568207 44568207 44568207 CCTCTTCCCCCGGCAGACATACTTTGAAGACAACCCTAGGGACCTCCAGCTGCTGCGGCATGACC CCTCTTCCCCCGGCAGACATACTTTGAAGACAGCCCTAGGGACCTCCAGCTGCTGCGGCATGACC T C DDX56 Ensembl:ENSG00000136271 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44568101..44568269 26863410 MeRIP-seq:(Medium) rs764434931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952461,Human_RBP_ID_1687041,Human_RBP_ID_2043350,Human_RBP_ID_3847394,Human_RBP_ID_3970874,Human_RBP_ID_5403949,Human_RBP_ID_7741685,Human_RBP_ID_8911029,Human_RBP_ID_9403347,Human_RBP_ID_16163837,Human_RBP_ID_18171877,Human_RBP_ID_18540217,Human_RBP_ID_19020731,Human_RBP_ID_22685384,Human_RBP_ID_22747057,Human_RBP_ID_26546876,Human_RBP_ID_27531798 Human_Splice_Rec_862958,Human_Splice_Rec_862959,Human_Splice_Rec_862984,Human_Splice_Rec_862985,Human_Splice_Rec_863010,Human_Splice_Rec_863011,Human_Splice_Rec_863038,Human_Splice_Rec_863039,Human_Splice_Rec_863062,Human_Splice_Rec_863063,Human_Splice_Rec_863086,Human_Splice_Rec_863087,Human_Splice_Rec_863110,Human_Splice_Rec_863111,Human_Splice_Rec_863120,Human_Splice_Rec_863121,Human_Splice_Rec_863142 Human_miRNA_ID_2293788 RMVar_hsa_circ_98480,RMVar_hsa_circ_269065,RMVar_hsa_circ_102648,RMVar_hsa_circ_99813,RMVar_hsa_circ_244956,RMVar_hsa_circ_244958,RMVar_hsa_circ_92304,RMVar_hsa_circ_244957,RMVar_hsa_circ_13874,RMVar_hsa_circ_244955,RMVar_hsa_circ_83731,RMVar_hsa_circ_269245,RMVar_hsa_circ_244960 96149 RMVar_ID_96149 Human_SNP_ID_318828442 m1A Human chr7 - 44570114 44570114 44570114 ATTGAGTTATCTCTGCAGGGCCTCTGATCCGGAAGCAGGTGTGGCCCGGGGCATAGACTTCCACC ATTGAGTTATCTCTGCAGGGCCTCTGATCCGGCAGCAGGTGTGGCCCGGGGCATAGACTTCCACC T G DDX56 Ensembl:ENSG00000136271 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44570064..44570793 32194978 MeRIP-seq:(Medium) rs1222549467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253490,Human_RBP_ID_793547,Human_RBP_ID_5403956,Human_RBP_ID_19020739,Human_RBP_ID_22747059 Human_Splice_Rec_862950,Human_Splice_Rec_862951,Human_Splice_Rec_862976,Human_Splice_Rec_862977,Human_Splice_Rec_863002,Human_Splice_Rec_863030,Human_Splice_Rec_863031,Human_Splice_Rec_863054,Human_Splice_Rec_863055,Human_Splice_Rec_863078,Human_Splice_Rec_863079,Human_Splice_Rec_863102,Human_Splice_Rec_863103,Human_Splice_Rec_863134,Human_Splice_Rec_863144 RMVar_hsa_circ_17987,RMVar_hsa_circ_98480,RMVar_hsa_circ_269065,RMVar_hsa_circ_102648,RMVar_hsa_circ_99813,RMVar_hsa_circ_244956,RMVar_hsa_circ_244958,RMVar_hsa_circ_92304,RMVar_hsa_circ_244957,RMVar_hsa_circ_111837,RMVar_hsa_circ_13874,RMVar_hsa_circ_244955,RMVar_hsa_circ_83731,RMVar_hsa_circ_269245,RMVar_hsa_circ_244960,RMVar_hsa_circ_244961,RMVar_hsa_circ_371707,RMVar_hsa_circ_375076,RMVar_hsa_circ_244962,RMVar_hsa_circ_8902,RMVar_hsa_circ_244963,RMVar_hsa_circ_98211,RMVar_hsa_circ_317037,RMVar_hsa_circ_334446,RMVar_hsa_circ_244964 96150 RMVar_ID_96150 Human_SNP_ID_318829356 m1A Human chr7 - 44573031 44573031 44573031 CATATTCTTACAGACAGGTCCGGTGGTAGAACAGGCAGTGAGAGGCCTTGTTCTTGTTCCTACCA CATATTCTTACAGACAGGTCCGGTGGTAGAACCGGCAGTGAGAGGCCTTGTTCTTGTTCCTACCA T G DDX56 Ensembl:ENSG00000136271 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44572876..44573050 26863196 MeRIP-seq:(Medium) rs747370127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952464,Human_RBP_ID_5533493,Human_RBP_ID_8911042,Human_RBP_ID_9351055,Human_RBP_ID_16163885 Human_Splice_Rec_862940,Human_Splice_Rec_862966,Human_Splice_Rec_862992,Human_Splice_Rec_863020,Human_Splice_Rec_863044,Human_Splice_Rec_863068,Human_Splice_Rec_863094,Human_Splice_Rec_863146 RMVar_hsa_circ_99813,RMVar_hsa_circ_244955,RMVar_hsa_circ_375076,RMVar_hsa_circ_244963,RMVar_hsa_circ_98211,RMVar_hsa_circ_244964,RMVar_hsa_circ_12133 96151 RMVar_ID_96151 Human_SNP_ID_318829675 m1A Human chr7 - 44573866 44573866 44573866 GCCATGGAGGACTCTGAAGCACTGGGCTTCGAACACATGGGCCTCGATCCCCGGCTCCTTCAGGT GCCATGGAGGACTCTGAAGCACTGGGCTTCGACCACATGGGCCTCGATCCCCGGCTCCTTCAGGT T G DDX56 Ensembl:ENSG00000136271 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:44573676..44573950 26863196 MeRIP-seq:(Medium) rs763773210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254312,Human_RBP_ID_954365,Human_RBP_ID_1687065,Human_RBP_ID_2043374,Human_RBP_ID_4956327,Human_RBP_ID_8667801,Human_RBP_ID_9404419,Human_RBP_ID_18171883,Human_RBP_ID_18451681,Human_RBP_ID_18883215,Human_RBP_ID_19020745,Human_RBP_ID_23080299,Human_RBP_ID_26355965,Human_RBP_ID_27113905 Human_Splice_Rec_862937,Human_Splice_Rec_862963,Human_Splice_Rec_862989,Human_Splice_Rec_863091,Human_Splice_Rec_863123 96152 RMVar_ID_96152 Human_SNP_ID_318830975 m1A Human chr7 + 44578487 44578487 44578487 CTCTGACTCTAAGGCCCTGTGGGATGAAAAGCAGGTATCCAAAAGAACTCTGCTTGGCCCTCTGA CTCTGACTCTAAGGCCCTGTGGGATGAAAAGCGGGTATCCAAAAGAACTCTGCTTGGCCCTCTGA A G NONHSAG047490.2 RNACentral:URS00009B0D60 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44578438..44578539 32194978 MeRIP-seq:(Medium) rs1463961840 Functional Loss SNV dbSNP153 33..33 33 - - - 96153 RMVar_ID_96153 Human_SNP_ID_318831908 m1A Human chr7 + 44581818 44581818 44581818 CTCCTTCTGCTTATCCCACATCTGGGTACGATAGTTGCCTGCGGGGCAGACACATAGTCACGACC CTCCTTCTGCTTATCCCACATCTGGGTACGATGGTTGCCTGCGGGGCAGACACATAGTCACGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44581719..44581857 26863196 MeRIP-seq:(Medium) rs1194771081 Functional Loss SNV dbSNP153 33..33 33 - - - 96154 RMVar_ID_96154 Human_SNP_ID_318832043 m1A Human chr7 - 44582124 44582124 44582124 GCTGCTTCTCGCGCTGTGCGCCACAGGCGCCCAGGGGCTCTACTTCCACATCGGCGAGACCGAGA GCTGCTTCTCGCGCTGTGCGCCACAGGCGCCCCGGGGCTCTACTTCCACATCGGCGAGACCGAGA T G TMED4 Ensembl:ENSG00000158604 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44582076..44582150 26863196 MeRIP-seq:(Medium) rs1426376278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684785,Human_RBP_ID_1052145,Human_RBP_ID_1687093,Human_RBP_ID_2043417,Human_RBP_ID_3847438,Human_RBP_ID_4955760,Human_RBP_ID_5327835,Human_RBP_ID_5429580,Human_RBP_ID_5513377,Human_RBP_ID_8911046,Human_RBP_ID_9211366,Human_RBP_ID_22463476,Human_RBP_ID_27531811 Human_Splice_Rec_863149,Human_Splice_Rec_863155,Human_Splice_Rec_863161,Human_Splice_Rec_863171 96155 RMVar_ID_96155 Human_SNP_ID_318832091 m1A Human chr7 - 44582201 44582201 44582201 GCGCAGGCGCTTAGGGGCTGAGGCGCGATGGCAGGTGTCGGGGCTGGGCCTCTGCGGGCGATGGG GCGCAGGCGCTTAGGGGCTGAGGCGCGATGGCCGGTGTCGGGGCTGGGCCTCTGCGGGCGATGGG T G TMED4 Ensembl:ENSG00000158604 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44582151..44582200 32194978 MeRIP-seq:(Medium) rs1431772842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955760,Human_RBP_ID_5327835,Human_RBP_ID_5513378,Human_RBP_ID_7741830,Human_RBP_ID_8667832,Human_RBP_ID_8911047,Human_RBP_ID_17672063,Human_RBP_ID_22463476,Human_RBP_ID_24216720 96156 RMVar_ID_96156 Human_SNP_ID_318838115 m1A Human chr7 + 44606652 44606652 44606652 GCGCCTCATTCGGGTGGAGCTGAGCCGGAGACAGGTAACCGTGCGCTGTCGCCGCGCCCGTCCCA GCGCCTCATTCGGGTGGAGCTGAGCCGGAGACGGGTAACCGTGCGCTGTCGCCGCGCCCGTCCCA A G OGDH Ensembl:ENSG00000105953 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44606639..44606729;chr7:44606601..44606977;chr7:44606601..44624450 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1434546514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956329,Human_RBP_ID_8914354,Human_RBP_ID_18425995,Human_RBP_ID_19136326 Human_Splice_Rec_863177,Human_Splice_Rec_863215,Human_Splice_Rec_863231,Human_Splice_Rec_863277,Human_Splice_Rec_863321,Human_Splice_Rec_863331,Human_Splice_Rec_863375,Human_Splice_Rec_863421 96157 RMVar_ID_96157 Human_SNP_ID_318838119 m1A Human chr7 - 44606661 44606661 44606661 ACCCGGCACTGGGACGGGCGCGGCGACAGCGCACGGTTACCTGTCTCCGGCTCAGCTCCACCCGA ACCCGGCACTGGGACGGGCGCGGCGACAGCGCCCGGTTACCTGTCTCCGGCTCAGCTCCACCCGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44606651..44606954 26863196 MeRIP-seq:(Medium) rs1255084384 Functional Loss SNV dbSNP153 33..33 33 - - - 96158 RMVar_ID_96158 Human_SNP_ID_318838126 m1A Human chr7 + 44606684 44606684 44606684 AGGTAACCGTGCGCTGTCGCCGCGCCCGTCCCAGTGCCGGGTGTCGCGGCGCTTGGCGGCCCGGG AGGTAACCGTGCGCTGTCGCCGCGCCCGTCCCGGTGCCGGGTGTCGCGGCGCTTGGCGGCCCGGG A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:44606674..44606994 26863196 MeRIP-seq:(Medium) rs1464457472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18425995,Human_RBP_ID_19136326 96159 RMVar_ID_96159 Human_SNP_ID_318838342 m1A Human chr7 - 44607190 44607190 44607190 GCGCCAAGGTCTGCGCGGTAATCCAAACAGGCAGTCCCACCCAGGGCCACCCCAAAGCCAGATGC GCGCCAAGGTCTGCGCGGTAATCCAAACAGGCTGTCCCACCCAGGGCCACCCCAAAGCCAGATGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44607184..44607269 26863196 MeRIP-seq:(Medium) rs1282825675 Functional Loss SNV dbSNP153 33..33 33 - - - 96160 RMVar_ID_96160 Human_SNP_ID_318843186 m1A Human chr7 - 44624303 44624303 44624303 TGAAGTTTTTCACAACTGCCTGTACAAAAAAAAAAAAAAAAAAACAAGAAAGAAAGGTTTTAAAA TGAAGTTTTTCACAACTGCCTGTACAAAAAAAGAAAAAAAAAAACAAGAAAGAAAGGTTTTAAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44624301..44624504 26863196 MeRIP-seq:(Medium) rs1308259487 Functional Loss SNV dbSNP153 33..33 33 - - - 96161 RMVar_ID_96161 Human_SNP_ID_318855505 m1A Human chr7 + 44673871 44673871 44673871 AGCAGTGCCAGTGGATCCGGCAGAAGTTTGAGACCCCTGGGATCATGCAGTTCACAAATGAGGAG AGCAGTGCCAGTGGATCCGGCAGAAGTTTGAGTCCCCTGGGATCATGCAGTTCACAAATGAGGAG A T OGDH Ensembl:ENSG00000105953 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44673822..44673967 26863196 MeRIP-seq:(Medium) rs1562660516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684792,Human_RBP_ID_8914356,Human_RBP_ID_9311785 Human_Splice_Rec_863224,Human_Splice_Rec_863225,Human_Splice_Rec_863242,Human_Splice_Rec_863243,Human_Splice_Rec_863286,Human_Splice_Rec_863287,Human_Splice_Rec_863340,Human_Splice_Rec_863341,Human_Splice_Rec_863386,Human_Splice_Rec_863387,Human_Splice_Rec_863430,Human_Splice_Rec_863431,Human_Splice_Rec_863464,Human_Splice_Rec_863465,Human_Splice_Rec_863470,Human_Splice_Rec_863471 Human_miRNA_ID_2234535,Human_miRNA_ID_2234536,Human_miRNA_ID_2516716,Human_miRNA_ID_2516717,Human_miRNA_ID_3028693,Human_miRNA_ID_3028694 RMVar_hsa_circ_77643,RMVar_hsa_circ_33602,RMVar_hsa_circ_92710,RMVar_hsa_circ_102585,RMVar_hsa_circ_119943,RMVar_hsa_circ_335507,RMVar_hsa_circ_244970,RMVar_hsa_circ_244971,RMVar_hsa_circ_339006,RMVar_hsa_circ_329689,RMVar_hsa_circ_123357,RMVar_hsa_circ_244980,RMVar_hsa_circ_244982,RMVar_hsa_circ_87767,RMVar_hsa_circ_244983,RMVar_hsa_circ_244981,RMVar_hsa_circ_18465,RMVar_hsa_circ_29218,RMVar_hsa_circ_244984,RMVar_hsa_circ_337603,RMVar_hsa_circ_266786,RMVar_hsa_circ_294363,RMVar_hsa_circ_118598,RMVar_hsa_circ_244987,RMVar_hsa_circ_244988,RMVar_hsa_circ_344891,RMVar_hsa_circ_348602,RMVar_hsa_circ_244989 96162 RMVar_ID_96162 Human_SNP_ID_318856368 m1A Human chr7 - 44676838 44676838 44676838 TTCTCCTTCAGGCTCACCTACACTTTTTCCTTACAGAGACTCTCAGACTCCCCTCCTTTTCAGTG TTCTCCTTCAGGCTCACCTACACTTTTTCCTTGCAGAGACTCTCAGACTCCCCTCCTTTTCAGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44676836..44676967 26863196 MeRIP-seq:(Medium) rs536486370 Functional Loss SNV dbSNP153 33..33 33 - - - 96163 RMVar_ID_96163 Human_SNP_ID_318864489 m1A Human chr7 + 44708042 44708042 44708042 GGGTTGCTTGGGCCACTGCCCTCTCCACACCCATGACTGCCCCTTGCTTCTCAACTAAAGAATAG GGGTTGCTTGGGCCACTGCCCTCTCCACACCCGTGACTGCCCCTTGCTTCTCAACTAAAGAATAG A G OGDH Ensembl:ENSG00000105953 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44707991..44708144 26863196 MeRIP-seq:(Medium) rs763914811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18100922,Human_RBP_ID_22463078,Human_RBP_ID_27531834,Human_RBP_ID_27569197 96164 RMVar_ID_96164 Human_SNP_ID_318874480 m1A Human chr7 - 44748886 44748866 44748886 TCCGCGCCGCCCGCCGCCCCGGGGCCGCCGCCACCCGCGCCATCGCGCCGCCGCCCGCTCCGAGG TCCGCGCCGCCCGCCGCCCCGGGGCCGCCGCC____________________GCCCGCTCCGAGG CGGCGGCGCGATGGCGCGGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr7:44748593..44749834;chr7:44748851..44749097 26863196 MeRIP-seq:(Medium) rs954108955 Functional Loss DEL dbSNP153 33..52 33 - - - 96165 RMVar_ID_96165 Human_SNP_ID_318874488 m1A Human chr7 - 44748886 44748886 44748886 TCCGCGCCGCCCGCCGCCCCGGGGCCGCCGCCACCCGCGCCATCGCGCCGCCGCCCGCTCCGAGG TCCGCGCCGCCCGCCGCCCCGGGGCCGCCGCCCCCCGCGCCATCGCGCCGCCGCCCGCTCCGAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr7:44748593..44749834;chr7:44748851..44749097 26863196 MeRIP-seq:(Medium) rs1183218714 Functional Loss SNV dbSNP153 33..33 33 - - - 96166 RMVar_ID_96166 Human_SNP_ID_318874502 m1A Human chr7 + 44748918 44748906 44748918 TGGCGGCGGCCCCGGGGCGGCGGGCGGCGCGGAGGGCGGGCTGAGCGCATGGAGCGGCGCGGGCC TGGCGGCGGCCCCGGGGCGGC____________GGGCGGGCTGAGCGCATGGAGCGGCGCGGGCC CGGGCGGCGCGGA C ZMIZ2 Ensembl:ENSG00000122515 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:44748826..44749396;chr7:44748826..44749361;chr7:44748851..44749263 26863196 MeRIP-seq:(Medium) rs1562715941 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_254052,Human_RBP_ID_4955763,Human_RBP_ID_5402990,Human_RBP_ID_18426311,Human_RBP_ID_27842880 Human_Splice_Rec_863507,Human_Splice_Rec_863543,Human_Splice_Rec_863553 96167 RMVar_ID_96167 Human_SNP_ID_318874713 m1A Human chr7 - 44749541 44749541 44749541 ATGTCCAGTTTGGAAAGGGGTGTCCCCATCAAAACTGGCAGCTGGGGGCTGGCCGCTCAGCGTCG ATGTCCAGTTTGGAAAGGGGTGTCCCCATCAACACTGGCAGCTGGGGGCTGGCCGCTCAGCGTCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44749490..44749687 32194978 MeRIP-seq:(Medium) rs1215369348 Functional Loss SNV dbSNP153 33..33 33 - - - 96168 RMVar_ID_96168 Human_SNP_ID_318876214 m1A Human chr7 - 44756133 44756133 44756133 TGTTAGCTGCGATGCAGCCAGGAGACCCTTTCAGCAGGGTGGAGGGACCCCGGTGCCAGCAGGCC TGTTAGCTGCGATGCAGCCAGGAGACCCTTTCGGCAGGGTGGAGGGACCCCGGTGCCAGCAGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:44756130..44756300 26863196 MeRIP-seq:(Medium) rs912446887 Functional Loss SNV dbSNP153 33..33 33 - - - 96169 RMVar_ID_96169 Human_SNP_ID_318876251 m1A Human chr7 - 44756244 44756244 44756244 AGGTTTCATGGGGTTCATGGAGTTCATTGGCAATGGAGCAGCCTACAGGCCGGGTCTGACAGTTT AGGTTTCATGGGGTTCATGGAGTTCATTGGCAGTGGAGCAGCCTACAGGCCGGGTCTGACAGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44756150..44756322 26863196 MeRIP-seq:(Medium) rs771425051 Functional Loss SNV dbSNP153 33..33 33 - - - 96170 RMVar_ID_96170 Human_SNP_ID_318877782 m1A Human chr7 - 44760592 44760592 44760592 ACCCCGCTGTCCCAAGAGTGGACAGACTTACCAGAGGGCGATGAGTGCAAGGAGTTGAGGTTGGG ACCCCGCTGTCCCAAGAGTGGACAGACTTACCGGAGGGCGATGAGTGCAAGGAGTTGAGGTTGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44760551..44760600 26863196 MeRIP-seq:(Medium) rs1189426710 Functional Loss SNV dbSNP153 33..33 33 - - - 96171 RMVar_ID_96171 Human_SNP_ID_318878025 m1A Human chr7 - 44761495 44761495 44761495 TGCTGCAGGCGGAAGGGCTCCAGGACCACCCCATCGCGCACAGGGAAGGTCAGCCGCAACTCGTC TGCTGCAGGCGGAAGGGCTCCAGGACCACCCCGTCGCGCACAGGGAAGGTCAGCCGCAACTCGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44760590..44763376 32194978 MeRIP-seq:(Medium) rs1329405799 Functional Loss SNV dbSNP153 33..33 33 - - - 96172 RMVar_ID_96172 Human_SNP_ID_318879176 m1A Human chr7 + 44765402 44765402 44765402 GCAGCTGGAAGCCAGTGCCCGTGAAGCCTGACATGCACATCAAGGAGGAGCCGGATGGGCCAGCA GCAGCTGGAAGCCAGTGCCCGTGAAGCCTGACGTGCACATCAAGGAGGAGCCGGATGGGCCAGCA A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44765351..44765575 26863196 MeRIP-seq:(Medium) rs1200184048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3971950,Human_RBP_ID_9404431,Human_RBP_ID_19020774,Human_RBP_ID_26356447,Human_RBP_ID_27830302 Human_Splice_Rec_863500,Human_Splice_Rec_863536,Human_Splice_Rec_863588,Human_Splice_Rec_863624,Human_Splice_Rec_863656,Human_Splice_Rec_863688,Human_Splice_Rec_863706,Human_Splice_Rec_863726,Human_Splice_Rec_863742,Human_Splice_Rec_863748 96173 RMVar_ID_96173 Human_SNP_ID_318879469 m1A Human chr7 + 44766252 44766252 44766252 AGCACCCCAACCCTTGCTGAGTTCACCCCGGGACCACCCCCCATCTCCTACCAGTCTGACATTCC AGCACCCCAACCCTTGCTGAGTTCACCCCGGGCCCACCCCCCATCTCCTACCAGTCTGACATTCC A C ZMIZ2 Ensembl:ENSG00000122515 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44766096..44766598 26863196 MeRIP-seq:(Medium) rs749050673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134809,Human_RBP_ID_17092860,Human_RBP_ID_18959222 Human_Splice_Rec_863502,Human_Splice_Rec_863503,Human_Splice_Rec_863538,Human_Splice_Rec_863539,Human_Splice_Rec_863590,Human_Splice_Rec_863591,Human_Splice_Rec_863626,Human_Splice_Rec_863627,Human_Splice_Rec_863658,Human_Splice_Rec_863659,Human_Splice_Rec_863690,Human_Splice_Rec_863691,Human_Splice_Rec_863708,Human_Splice_Rec_863709,Human_Splice_Rec_863728,Human_Splice_Rec_863729,Human_Splice_Rec_863750,Human_Splice_Rec_863751,Human_Splice_Rec_863755 96174 RMVar_ID_96174 Human_SNP_ID_318879477 m1A Human chr7 - 44766263 44766263 44766263 GGAGGCTGCTGGGAATGTCAGACTGGTAGGAGATGGGGGGTGGTCCCGGGGTGAACTCAGCAAGG GGAGGCTGCTGGGAATGTCAGACTGGTAGGAGGTGGGGGGTGGTCCCGGGGTGAACTCAGCAAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44766176..44766275 26863196 MeRIP-seq:(Medium) rs772185772 Functional Loss SNV dbSNP153 33..33 33 - - - 96175 RMVar_ID_96175 Human_SNP_ID_318879554 m1A Human chr7 + 44766432 44766432 44766432 AATTCTTCTCTCTGTCTTCAGATGGCACCAGCAGGTCACCTGGACCCCACTCACAATCCTGGGAC AATTCTTCTCTCTGTCTTCAGATGGCACCAGCGGGTCACCTGGACCCCACTCACAATCCTGGGAC A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44766422..44766487 26863196 MeRIP-seq:(Medium) rs1417168464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684825,Human_RBP_ID_8911065,Human_RBP_ID_9404433,Human_RBP_ID_19020777 Human_Splice_Rec_863504,Human_Splice_Rec_863540,Human_Splice_Rec_863592,Human_Splice_Rec_863628,Human_Splice_Rec_863660,Human_Splice_Rec_863692,Human_Splice_Rec_863710,Human_Splice_Rec_863730,Human_Splice_Rec_863752,Human_Splice_Rec_863756 96176 RMVar_ID_96176 Human_SNP_ID_318879576 m1A Human chr7 + 44766484 44766484 44766484 ACAATCCTGGGACACCAGGACTACACACCTCCAACCTTGGGGCCCCTCCAGGTCCCCAGCTGCAC ACAATCCTGGGACACCAGGACTACACACCTCCGACCTTGGGGCCCCTCCAGGTCCCCAGCTGCAC A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44766347..44766600;chr7:44766426..44766550 26863196 MeRIP-seq:(Medium) rs764732978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684826,Human_RBP_ID_1332369,Human_RBP_ID_1398909,Human_RBP_ID_17312999,Human_RBP_ID_17425557,Human_RBP_ID_17541450,Human_RBP_ID_27531844 Human_Splice_Rec_863504,Human_Splice_Rec_863540,Human_Splice_Rec_863592,Human_Splice_Rec_863628,Human_Splice_Rec_863660,Human_Splice_Rec_863692,Human_Splice_Rec_863710,Human_Splice_Rec_863730,Human_Splice_Rec_863752,Human_Splice_Rec_863756 96177 RMVar_ID_96177 Human_SNP_ID_318879910 m1A Human chr7 + 44767503 44767503 44767503 CCAGTCAGTGACCAAAGCTGCTAACAGAGTTCACTTTGTCCTCAGCTGCTCCCGGAACTGACCAA CCAGTCAGTGACCAAAGCTGCTAACAGAGTTCCCTTTGTCCTCAGCTGCTCCCGGAACTGACCAA A C ZMIZ2 Ensembl:ENSG00000122515 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44767501..44767525 26863196 MeRIP-seq:(Medium) rs748732406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23077086 96178 RMVar_ID_96178 Human_SNP_ID_318879911 m1A Human chr7 + 44767503 44767503 44767503 CCAGTCAGTGACCAAAGCTGCTAACAGAGTTCACTTTGTCCTCAGCTGCTCCCGGAACTGACCAA CCAGTCAGTGACCAAAGCTGCTAACAGAGTTCGCTTTGTCCTCAGCTGCTCCCGGAACTGACCAA A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44767501..44767525 26863196 MeRIP-seq:(Medium) rs748732406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23077086 96179 RMVar_ID_96179 Human_SNP_ID_318880006 m1A Human chr7 - 44767772 44767765 44767773 ATCGAGCACAGGGCTGCTTCCAATTCAGGGGCAGGGCTGGCGGCAGAAGGCTCTGGCTCCAGGTG ATCGAGCACAGGGCTGCTTCCAATTCAGGGG________GCGGCAGAAGGCTCTGGCTCCAGGTG CCAGCCCTG C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44767726..44767775 26863196 MeRIP-seq:(Medium) rs887956079 Functional Loss DEL dbSNP153 32..39 33 - - - 96180 RMVar_ID_96180 Human_SNP_ID_318880009 m1A Human chr7 + 44767787 44767787 44767787 CCTTCTGCCGCCAGCCCTGCCCCTGAATTGGAAGCAGCCCTGTGCTCGATGGGAGGGGCTCCCAG CCTTCTGCCGCCAGCCCTGCCCCTGAATTGGAGGCAGCCCTGTGCTCGATGGGAGGGGCTCCCAG A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:44767501..44768000 26863196 MeRIP-seq:(Medium) rs1389086339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254221,Human_RBP_ID_684833 96181 RMVar_ID_96181 Human_SNP_ID_318887365 m1A Human chr7 + 44796695 44796695 44796695 GGAGGCCAGGCTCGTGCCGTTTTGCAGACGCCACCGCCGAGGAAAACCGTGTACTATTAGCCATG GGAGGCCAGGCTCGTGCCGTTTTGCAGACGCCGCCGCCGAGGAAAACCGTGTACTATTAGCCATG A G PPIA Ensembl:ENSG00000196262 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:44796676..44798008 26863196 MeRIP-seq:(Medium) rs756501298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253817,Human_RBP_ID_684871,Human_RBP_ID_794013,Human_RBP_ID_1221611,Human_RBP_ID_1398910,Human_RBP_ID_1687113,Human_RBP_ID_4956331,Human_RBP_ID_5153199,Human_RBP_ID_5243253,Human_RBP_ID_8667943,Human_RBP_ID_9211379,Human_RBP_ID_9337133,Human_RBP_ID_18100966,Human_RBP_ID_18426610,Human_RBP_ID_18883316,Human_RBP_ID_21904019,Human_RBP_ID_22109415,Human_RBP_ID_22323567,Human_RBP_ID_22463079,Human_RBP_ID_22835150,Human_RBP_ID_23081697,Human_RBP_ID_23215485,Human_RBP_ID_24216815,Human_RBP_ID_26725479,Human_RBP_ID_27114018,Human_RBP_ID_27357807,Human_RBP_ID_27531855 Human_Splice_Rec_863759,Human_Splice_Rec_863763,Human_Splice_Rec_863769,Human_Splice_Rec_863779,Human_Splice_Rec_863789,Human_Splice_Rec_863795,Human_Splice_Rec_863803,Human_Splice_Rec_863809 Human_miRNA_ID_2017739 RMVar_hsa_circ_86560,RMVar_hsa_circ_111598,RMVar_hsa_circ_127236,RMVar_hsa_circ_107790,RMVar_hsa_circ_245004,RMVar_hsa_circ_245006,RMVar_hsa_circ_245007,RMVar_hsa_circ_245005 96182 RMVar_ID_96182 Human_SNP_ID_318888057 m1A Human chr7 - 44798729 44798729 44798729 TCCAGGCCCCTTACCTAGTAGTGGGGTAAAAAATAAAGATTGGTTTCTAGTATATCTGGTTTTGA TCCAGGCCCCTTACCTAGTAGTGGGGTAAAAAGTAAAGATTGGTTTCTAGTATATCTGGTTTTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44798726..44798800 26863196 MeRIP-seq:(Medium) rs1286837842 Functional Loss SNV dbSNP153 33..33 33 - - - 96183 RMVar_ID_96183 Human_SNP_ID_318888186 m1A Human chr7 + 44799227 44799227 44799227 TACTAAGCAACAAAATAAGCAGATGTTAATTAACTGTAATTTTCTCTTACAGCTGTTTGCAGACA TACTAAGCAACAAAATAAGCAGATGTTAATTACCTGTAATTTTCTCTTACAGCTGTTTGCAGACA A C PPIA Ensembl:ENSG00000196262 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr7:44799226..44799300 26863196 MeRIP-seq:(Medium) rs775088233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953638,Human_RBP_ID_3090440,Human_RBP_ID_5401498,Human_RBP_ID_22622862,Human_RBP_ID_22685404,Human_RBP_ID_22746878,Human_RBP_ID_26105632 Human_Splice_Rec_863761,Human_Splice_Rec_863765,Human_Splice_Rec_863773,Human_Splice_Rec_863783,Human_Splice_Rec_863797,Human_Splice_Rec_863811,Human_Splice_Rec_863817,Human_Splice_Rec_863823 Human_miRNA_ID_2922235 RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_111598,RMVar_hsa_circ_127236,RMVar_hsa_circ_107790,RMVar_hsa_circ_245004,RMVar_hsa_circ_245006,RMVar_hsa_circ_245007,RMVar_hsa_circ_245005,RMVar_hsa_circ_109107,RMVar_hsa_circ_370389,RMVar_hsa_circ_245008,RMVar_hsa_circ_245009,RMVar_hsa_circ_245010 96184 RMVar_ID_96184 Human_SNP_ID_318888187 m1A Human chr7 + 44799227 44799227 44799227 TACTAAGCAACAAAATAAGCAGATGTTAATTAACTGTAATTTTCTCTTACAGCTGTTTGCAGACA TACTAAGCAACAAAATAAGCAGATGTTAATTAGCTGTAATTTTCTCTTACAGCTGTTTGCAGACA A G PPIA Ensembl:ENSG00000196262 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr7:44799226..44799300 26863196 MeRIP-seq:(Medium) rs775088233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953638,Human_RBP_ID_3090440,Human_RBP_ID_5401498,Human_RBP_ID_22622862,Human_RBP_ID_22685404,Human_RBP_ID_22746878,Human_RBP_ID_26105632 Human_Splice_Rec_863761,Human_Splice_Rec_863765,Human_Splice_Rec_863773,Human_Splice_Rec_863783,Human_Splice_Rec_863797,Human_Splice_Rec_863811,Human_Splice_Rec_863817,Human_Splice_Rec_863823 Human_miRNA_ID_2922235 RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_111598,RMVar_hsa_circ_127236,RMVar_hsa_circ_107790,RMVar_hsa_circ_245004,RMVar_hsa_circ_245006,RMVar_hsa_circ_245007,RMVar_hsa_circ_245005,RMVar_hsa_circ_109107,RMVar_hsa_circ_370389,RMVar_hsa_circ_245008,RMVar_hsa_circ_245009,RMVar_hsa_circ_245010 96185 RMVar_ID_96185 Human_SNP_ID_318888188 m1A Human chr7 - 44799229 44799228 44799230 CTTGTCTGCAAACAGCTGTAAGAGAAAATTACAGTTAATTAACATCTGCTTATTTTGTTGCTTAG CTTGTCTGCAAACAGCTGTAAGAGAAAATTA__GTTAATTAACATCTGCTTATTTTGTTGCTTAG CTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44799226..44799300 26863196 MeRIP-seq:(Medium) rs765384813 Functional Loss DEL dbSNP153 32..33 33 - - - 96186 RMVar_ID_96186 Human_SNP_ID_318888189 m1A Human chr7 - 44799229 44799229 44799229 CTTGTCTGCAAACAGCTGTAAGAGAAAATTACAGTTAATTAACATCTGCTTATTTTGTTGCTTAG CTTGTCTGCAAACAGCTGTAAGAGAAAATTACGGTTAATTAACATCTGCTTATTTTGTTGCTTAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44799226..44799300 26863196 MeRIP-seq:(Medium) rs1205143060 Functional Loss SNV dbSNP153 33..33 33 - - - 96187 RMVar_ID_96187 Human_SNP_ID_318888262 m1A Human chr7 - 44799380 44799380 44799380 TGCTCAGAGCACGAAAATTTTCTGTTTAAAAAAAAATTAAACACATATATACATACATAAAAATA TGCTCAGAGCACGAAAATTTTCTGTTTAAAAACAAATTAAACACATATATACATACATAAAAATA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr7:44799376..44799425 26863196 MeRIP-seq:(Medium) rs1418247362 Functional Loss SNV dbSNP153 33..33 33 - - - 96188 RMVar_ID_96188 Human_SNP_ID_318897523 m1A Human chr7 - 44832701 44832701 44832701 CAAGCCATCCTCCCACCTTGGCCTCCCAAAGTACTGGGATTATAGGCATAAGCCACCATGCCCTG CAAGCCATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATAAGCCACCATGCCCTG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1133201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 96189 RMVar_ID_96189 Human_SNP_ID_318897524 m1A Human chr7 - 44832704 44832704 44832704 GCTCAAGCCATCCTCCCACCTTGGCCTCCCAAAGTACTGGGATTATAGGCATAAGCCACCATGCC GCTCAAGCCATCCTCCCACCTTGGCCTCCCAAGGTACTGGGATTATAGGCATAAGCCACCATGCC T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1326053574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 96190 RMVar_ID_96190 Human_SNP_ID_318899717 m1A Human chr7 - 44840854 44840854 44840854 ATGTCTGTTGTATATGGCCATCCAGAAGGTGCACTAGTCTCAGTGACAGAAACCCATGGAATATA ATGTCTGTTGTATATGGCCATCCAGAAGGTGCGCTAGTCTCAGTGACAGAAACCCATGGAATATA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44840852..44841025 26863196 MeRIP-seq:(Medium) rs1418538234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16166434 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017,RMVar_hsa_circ_292601 96191 RMVar_ID_96191 Human_SNP_ID_318899725 m1A Human chr7 + 44840878 44840878 44840878 GAGACTAGTGCACCTTCTGGATGGCCATATACAACAGACATTCCTGTACAAACCTCTGCAGTGAG GAGACTAGTGCACCTTCTGGATGGCCATATACGACAGACATTCCTGTACAAACCTCTGCAGTGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44840876..44840975 32194978 MeRIP-seq:(Medium) rs1242967991 Functional Loss SNV dbSNP153 33..33 33 - - - 96192 RMVar_ID_96192 Human_SNP_ID_318899738 m1A Human chr7 + 44840905 44840905 44840905 TATACAACAGACATTCCTGTACAAACCTCTGCAGTGAGGTACTCCAGAATCGCAGCACTGTACAC TATACAACAGACATTCCTGTACAAACCTCTGCGGTGAGGTACTCCAGAATCGCAGCACTGTACAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44835526..44848083 32194978 MeRIP-seq:(Medium) rs760421407 Functional Loss SNV dbSNP153 33..33 33 - - - 96193 RMVar_ID_96193 Human_SNP_ID_318901680 m1A Human chr7 - 44847987 44847987 44847987 CAGCGGGAGGGCGCGCGGCCGAGCGGAGGCGGAGTCGGCGCCGAGAACATGGTAAGGGCGGCCGG CAGCGGGAGGGCGCGCGGCCGAGCGGAGGCGGCGTCGGCGCCGAGAACATGGTAAGGGCGGCCGG T G H2AZ2 Ensembl:ENSG00000105968 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr7:44843318..44848100;chr7:44840844..44848150 26863196 MeRIP-seq:(Medium) rs757636914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843710,Human_RBP_ID_4955765,Human_RBP_ID_5327841,Human_RBP_ID_8944159,Human_RBP_ID_9337139,Human_RBP_ID_18426524,Human_RBP_ID_22463477 Human_Splice_Rec_863829,Human_Splice_Rec_863837,Human_Splice_Rec_863843,Human_Splice_Rec_863851,Human_Splice_Rec_863857,Human_Splice_Rec_863863,Human_Splice_Rec_863869,Human_Splice_Rec_863873 RMVar_hsa_circ_93740,RMVar_hsa_circ_245020 96194 RMVar_ID_96194 Human_SNP_ID_318901688 m1A Human chr7 - 44847998 44847998 44847998 GCGCGGGTCGGCAGCGGGAGGGCGCGCGGCCGAGCGGAGGCGGAGTCGGCGCCGAGAACATGGTA GCGCGGGTCGGCAGCGGGAGGGCGCGCGGCCGGGCGGAGGCGGAGTCGGCGCCGAGAACATGGTA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44835564..44848083 26863410 MeRIP-seq:(Medium) rs780542193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792973,Human_RBP_ID_843710,Human_RBP_ID_4955765,Human_RBP_ID_5327841,Human_RBP_ID_8944159,Human_RBP_ID_9337139,Human_RBP_ID_18426524,Human_RBP_ID_22463477 Human_Splice_Rec_863829,Human_Splice_Rec_863837,Human_Splice_Rec_863843,Human_Splice_Rec_863851,Human_Splice_Rec_863857,Human_Splice_Rec_863863,Human_Splice_Rec_863869,Human_Splice_Rec_863873 RMVar_hsa_circ_93740,RMVar_hsa_circ_245020 96195 RMVar_ID_96195 Human_SNP_ID_318901689 m1A Human chr7 - 44847998 44847998 44847998 GCGCGGGTCGGCAGCGGGAGGGCGCGCGGCCGAGCGGAGGCGGAGTCGGCGCCGAGAACATGGTA GCGCGGGTCGGCAGCGGGAGGGCGCGCGGCCGCGCGGAGGCGGAGTCGGCGCCGAGAACATGGTA T G H2AZ2 Ensembl:ENSG00000105968 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44835564..44848083 26863410 MeRIP-seq:(Medium) rs780542193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792973,Human_RBP_ID_843710,Human_RBP_ID_4955765,Human_RBP_ID_5327841,Human_RBP_ID_8944159,Human_RBP_ID_9337139,Human_RBP_ID_18426524,Human_RBP_ID_22463477 Human_Splice_Rec_863829,Human_Splice_Rec_863837,Human_Splice_Rec_863843,Human_Splice_Rec_863851,Human_Splice_Rec_863857,Human_Splice_Rec_863863,Human_Splice_Rec_863869,Human_Splice_Rec_863873 RMVar_hsa_circ_93740,RMVar_hsa_circ_245020 96196 RMVar_ID_96196 Human_SNP_ID_318901725 m1A Human chr7 - 44848045 44848045 44848045 GTCCGGCTCCGGCGGCGGCGGTCGGTGCTGCGAGAGCGGCGGCGGCGGCGCGGGTCGGCAGCGGG GTCCGGCTCCGGCGGCGGCGGTCGGTGCTGCGGGAGCGGCGGCGGCGGCGCGGGTCGGCAGCGGG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,untreat control;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr7:44847876..44848100;chr7:44847951..44848089;chr7:44840841..44848159;chr7:44847904..44848100 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs867307115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253119,Human_RBP_ID_4955765,Human_RBP_ID_5327841,Human_RBP_ID_9337139,Human_RBP_ID_18425998,Human_RBP_ID_22463967 Human_Splice_Rec_863829,Human_Splice_Rec_863837,Human_Splice_Rec_863843,Human_Splice_Rec_863851,Human_Splice_Rec_863857,Human_Splice_Rec_863863,Human_Splice_Rec_863869,Human_Splice_Rec_863873 RMVar_hsa_circ_93740,RMVar_hsa_circ_245020 96197 RMVar_ID_96197 Human_SNP_ID_318911292 m1A Human chr7 - 44884716 44884716 44884716 GCAGGCGGCCCGGGAGGCGGCGCCGGGGGCCCAGGGGGCGGCCTGTATGGAGAGCTCCCGGAGGG GCAGGCGGCCCGGGAGGCGGCGCCGGGGGCCCGGGGGGCGGCCTGTATGGAGAGCTCCCGGAGGG T C PURB Ensembl:ENSG00000146676 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:44884667..44885150 26863196 MeRIP-seq:(Medium) rs1479647500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18101209 96198 RMVar_ID_96198 Human_SNP_ID_318911335 m1A Human chr7 - 44884777 44884777 44884777 CGAGTTCCGCGACGCGCTGGCGAAGCTCATAGACGACTACGGAGGCGAGGACGACGAGCTGGCAG CGAGTTCCGCGACGCGCTGGCGAAGCTCATAGGCGACTACGGAGGCGAGGACGACGAGCTGGCAG T C PURB Ensembl:ENSG00000146676 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:44884726..44884800 26863196 MeRIP-seq:(Medium) rs866037798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2043709,Human_RBP_ID_8911420 96199 RMVar_ID_96199 Human_SNP_ID_318911416 m1A Human chr7 + 44884993 44884993 44884993 TGCGGTTCTCACGCACCAAGAATTCGCTCTTGAGCGCGCGCCGCGGCCCGCCGCCCTCCTCGGCG TGCGGTTCTCACGCACCAAGAATTCGCTCTTGCGCGCGCGCCGCGGCCCGCCGCCCTCCTCGGCG A C AC004854.2 Ensembl:ENSG00000272768 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44884952..44885251 32194978 MeRIP-seq:(Medium) rs866123156 Functional Loss SNV dbSNP153 33..33 33 - - - 96200 RMVar_ID_96200 Human_SNP_ID_318911590 m1A Human chr7 - 44885365 44885357 44885365 CGGGGGCGCGAGCGCGGCGGGCGGTGGCGGCGAGGCGGCGGCCTAGAAGATGGCGGACGGCGACA CGGGGGCGCGAGCGCGGCGGGCGGTGGCGGCG________GCCTAGAAGATGGCGGACGGCGACA CCGCCGCCT C PURB Ensembl:ENSG00000146676 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr7:44885211..44885500;chr7:44884354..44885525 26863196 MeRIP-seq:(Medium) rs1437167618 Functional Loss DEL dbSNP153 33..40 33 - - - 96201 RMVar_ID_96201 Human_SNP_ID_318911652 m1A Human chr7 - 44885491 44885472 44885492 CACGGAAGTCGCGGGGGCGGGGCGCGGAGGCGATGGGGGGGCGGCGGCGGCCGGCGATGAGCGGC CACGGAAGTCGCGGGGGCGGGGCGCGGAGGC____________________CGGCGATGAGCGGC GGCCGCCGCCGCCCCCCCATC G PURB Ensembl:ENSG00000146676 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:44885407..44885492 26863410 MeRIP-seq:(Medium) rs1481108654 Functional Loss DEL dbSNP153 32..51 33 - - - Human_RBP_ID_24217075 96202 RMVar_ID_96202 Human_SNP_ID_318911680 m1A Human chr7 - 44885491 44885491 44885491 CACGGAAGTCGCGGGGGCGGGGCGCGGAGGCGATGGGGGGGCGGCGGCGGCCGGCGATGAGCGGC CACGGAAGTCGCGGGGGCGGGGCGCGGAGGCGTTGGGGGGGCGGCGGCGGCCGGCGATGAGCGGC T A PURB Ensembl:ENSG00000146676 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:44885407..44885492 26863410 MeRIP-seq:(Medium) rs960969182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24217075 96203 RMVar_ID_96203 Human_SNP_ID_318913242 m1A Human chr7 - 44891509 44891508 44891509 TCCTGCCCCTGCATTTACTTGTGAGCGTTCTGACATCTGGCTTCCATCCCCTGGGGCCCCAAAGT TCCTGCCCCTGCATTTACTTGTGAGCGTTCTG_CATCTGGCTTCCATCCCCTGGGGCCCCAAAGT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44891490..44891734 26863196 MeRIP-seq:(Medium) rs1257266588 Functional Loss DEL dbSNP153 33..33 33 - - - 96204 RMVar_ID_96204 Human_SNP_ID_318913277 m1A Human chr7 - 44891622 44891621 44891623 CTCAGAGCTGGCTCAGGTTTCTCTGGGGTAAAACAGCCTTCATCCTGCCTTCCTTTGCCAGTACC CTCAGAGCTGGCTCAGGTTTCTCTGGGGTAA__CAGCCTTCATCCTGCCTTCCTTTGCCAGTACC GTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:44891477..44891732 26863196 MeRIP-seq:(Medium) rs1459725577 Functional Loss DEL dbSNP153 32..33 33 - - - 96205 RMVar_ID_96205 Human_SNP_ID_318938049 m1A Human chr7 - 44986571 44986571 44986571 CAGCGGCGCGGTCTTCGGCAGTCTAGTCATCCACCGCCATCCTGGGCCCCACGTGTTGCCTGACC CAGCGGCGCGGTCTTCGGCAGTCTAGTCATCCGCCGCCATCCTGGGCCCCACGTGTTGCCTGACC T C SNHG15 Ensembl:ENSG00000232956 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44986179..44986625 26863196 MeRIP-seq:(Medium) rs957904546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1332398,Human_RBP_ID_1687370,Human_RBP_ID_4956338,Human_RBP_ID_5152935,Human_RBP_ID_5513396,Human_RBP_ID_5627555,Human_RBP_ID_5657857,Human_RBP_ID_16167217,Human_RBP_ID_26830346,Human_RBP_ID_27114149 Human_Splice_Rec_864149,Human_Splice_Rec_864155,Human_Splice_Rec_864163,Human_Splice_Rec_864169,Human_Splice_Rec_864175,Human_Splice_Rec_864183,Human_Splice_Rec_864187,Human_Splice_Rec_864193,Human_Splice_Rec_864197,Human_Splice_Rec_864199,Human_Splice_Rec_864203,Human_Splice_Rec_864209,Human_Splice_Rec_864217 96206 RMVar_ID_96206 Human_SNP_ID_318938050 m1A Human chr7 - 44986571 44986571 44986571 CAGCGGCGCGGTCTTCGGCAGTCTAGTCATCCACCGCCATCCTGGGCCCCACGTGTTGCCTGACC CAGCGGCGCGGTCTTCGGCAGTCTAGTCATCCCCCGCCATCCTGGGCCCCACGTGTTGCCTGACC T G SNHG15 Ensembl:ENSG00000232956 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44986179..44986625 26863196 MeRIP-seq:(Medium) rs957904546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1332398,Human_RBP_ID_1687370,Human_RBP_ID_4956338,Human_RBP_ID_5152935,Human_RBP_ID_5513396,Human_RBP_ID_5627555,Human_RBP_ID_5657857,Human_RBP_ID_16167217,Human_RBP_ID_26830346,Human_RBP_ID_27114149 Human_Splice_Rec_864149,Human_Splice_Rec_864155,Human_Splice_Rec_864163,Human_Splice_Rec_864169,Human_Splice_Rec_864175,Human_Splice_Rec_864183,Human_Splice_Rec_864187,Human_Splice_Rec_864193,Human_Splice_Rec_864197,Human_Splice_Rec_864199,Human_Splice_Rec_864203,Human_Splice_Rec_864209,Human_Splice_Rec_864217 96207 RMVar_ID_96207 Human_SNP_ID_520858532 m1A Human chr12 + 130790881 130790881 130790881 CGGAAACGGAGCTGAGGCCGAGGCTTTTCTGGAGGGCACCAGCACATTTAAACTCACAGAAGGCA CGGAAACGGAGCTGAGGCCGAGGCTTTTCTGGGGGGCACCAGCACATTTAAACTCACAGAAGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:130790837..130790980 26863196 MeRIP-seq:(Medium) rs1181373243 Functional Loss SNV dbSNP153 33..33 33 - - - 96208 RMVar_ID_96208 Human_SNP_ID_520868069 m1A Human chr12 - 130827269 130827269 130827269 TTTAAAAAACTGAATTTTCCATTTTTCATTGTAGTGTAGGAAGAATGATGATGGAGACACAGTTG TTTAAAAAACTGAATTTTCCATTTTTCATTGTGGTGTAGGAAGAATGATGATGGAGACACAGTTG T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:130827245..130827343 26863410 MeRIP-seq:(Medium) rs1317503125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4252575 Human_Splice_Rec_1444667,Human_Splice_Rec_1444687,Human_Splice_Rec_1444707 96209 RMVar_ID_96209 Human_SNP_ID_520871239 m1A Human chr12 - 130839137 130839137 130839137 AGCCCGAGGCCCGGCCGGAGGCAGCTCGGGACAGGCTTGAGCGGCGGGGCGCGCTGCCCGGCCGG AGCCCGAGGCCCGGCCGGAGGCAGCTCGGGACCGGCTTGAGCGGCGGGGCGCGCTGCCCGGCCGG T G STX2 Ensembl:ENSG00000111450 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:130839116..130839216 26863410 MeRIP-seq:(Medium) rs1260933386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754641,Human_RBP_ID_4248021,Human_RBP_ID_18978231 Human_Splice_Rec_1444665,Human_Splice_Rec_1444685 96210 RMVar_ID_96210 Human_SNP_ID_520881456 m1A Human chr12 + 130872309 130872309 130872309 CCGGGGCAGGAGACGGGCGTGGGGTCGGCGCTAGCCCCCGCGAACCCCCGTTTCATCCTCCGCTC CCGGGGCAGGAGACGGGCGTGGGGTCGGCGCTGGCCCCCGCGAACCCCCGTTTCATCCTCCGCTC A G RAN Ensembl:ENSG00000132341 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:130872301..130872522 26863196 MeRIP-seq:(Medium) rs1233352369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260194,Human_RBP_ID_3418645,Human_RBP_ID_9416668,Human_RBP_ID_19057179,Human_RBP_ID_26776942 RMVar_hsa_circ_123982,RMVar_hsa_circ_125078,RMVar_hsa_circ_161713,RMVar_hsa_circ_121066,RMVar_hsa_circ_161714,RMVar_hsa_circ_161712 96211 RMVar_ID_96211 Human_SNP_ID_520881630 m1A Human chr12 - 130872631 130872631 130872631 GCTCGGCCGCCTCCCGCCCCGCAGGGTTACCTACTTTGAACTGGACCTGGGGCTCTCCCTGCGCA GCTCGGCCGCCTCCCGCCCCGCAGGGTTACCTTCTTTGAACTGGACCTGGGGCTCTCCCTGCGCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:130872574..130872675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96212 RMVar_ID_96212 Human_SNP_ID_520881631 m1A Human chr12 - 130872631 130872631 130872631 GCTCGGCCGCCTCCCGCCCCGCAGGGTTACCTACTTTGAACTGGACCTGGGGCTCTCCCTGCGCA GCTCGGCCGCCTCCCGCCCCGCAGGGTTACCTGCTTTGAACTGGACCTGGGGCTCTCCCTGCGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:130872574..130872675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96213 RMVar_ID_96213 Human_SNP_ID_520881816 m1A Human chr12 + 130873126 130873126 130873126 ATTCGGTGGACTGAGAGATGGCTATTATATCCAAGGTAGGCATTTGTAACTTGCTGAACGGTTTT ATTCGGTGGACTGAGAGATGGCTATTATATCCGAGGTAGGCATTTGTAACTTGCTGAACGGTTTT A G RAN Ensembl:ENSG00000132341 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:130873076..130873150 26863196 MeRIP-seq:(Medium) rs1291083991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1467797,Human_RBP_ID_1790532,Human_RBP_ID_9323370,Human_RBP_ID_9344814,Human_RBP_ID_11875652,Human_RBP_ID_17813168,Human_RBP_ID_19059794,Human_RBP_ID_22437523,Human_RBP_ID_23547576,Human_RBP_ID_26806342,Human_RBP_ID_27425935 Human_Splice_Rec_1444729,Human_Splice_Rec_1444739,Human_Splice_Rec_1444749,Human_Splice_Rec_1444761,Human_Splice_Rec_1444771,Human_Splice_Rec_1444779,Human_Splice_Rec_1444791,Human_Splice_Rec_1444813 RMVar_hsa_circ_123982,RMVar_hsa_circ_125078,RMVar_hsa_circ_161713,RMVar_hsa_circ_161714 96214 RMVar_ID_96214 Human_SNP_ID_520882337 m1A Human chr12 + 130874530 130874530 130874530 ACTTGTGCAGTAAACTGAGTGTACTAATTCCCACAAATGTTTCTTCAGCCCAGTGTGCCATCATA ACTTGTGCAGTAAACTGAGTGTACTAATTCCCGCAAATGTTTCTTCAGCCCAGTGTGCCATCATA A G RAN Ensembl:ENSG00000132341 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:130874526..130874750 32194978 MeRIP-seq:(Medium) rs1307615265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875435,Human_RBP_ID_2313440,Human_RBP_ID_9344815,Human_RBP_ID_22645615 RMVar_hsa_circ_123982,RMVar_hsa_circ_125078,RMVar_hsa_circ_161713,RMVar_hsa_circ_161714 96215 RMVar_ID_96215 Human_SNP_ID_520882993 m1A Human chr12 + 130876634 130876634 130876634 GTCAGAATAAAAATGTGGTTTGTACATATCAAATAGATATTTTAAGGGTAATATTTTCTTTTATG GTCAGAATAAAAATGTGGTTTGTACATATCAAGTAGATATTTTAAGGGTAATATTTTCTTTTATG A G RAN Ensembl:ENSG00000132341 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:130876583..130876733 32194978 MeRIP-seq:(Medium) rs185042554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415012,Human_RBP_ID_990762,Human_RBP_ID_2313464,Human_RBP_ID_3398093,Human_RBP_ID_6152447,Human_RBP_ID_17237153,Human_RBP_ID_17352818,Human_RBP_ID_17813181,Human_RBP_ID_18257381,Human_RBP_ID_26609763,Human_RBP_ID_27624860 96216 RMVar_ID_96216 Human_SNP_ID_520903760 m1A Human chr12 + 130954036 130954036 130954036 GGCGGGCGCTCCAGGGGAAAACCACGCACAAAACCTTCTTCAGAGAAAAGGGAAGCTCCAAACCT GGCGGGCGCTCCAGGGGAAAACCACGCACAAACCCTTCTTCAGAGAAAAGGGAAGCTCCAAACCT A C ADGRD1 Ensembl:ENSG00000111452 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:130953987..130954053 26863196 MeRIP-seq:(Medium) rs1015355234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161720 96217 RMVar_ID_96217 Human_SNP_ID_520920484 m1A Human chr12 + 131014479 131014479 131014479 GCCGGCCCGAACTGGAATCTTCCTCTCCCTGGAGCTCCTTCTCTTGGGCCTTTGTTTCTGAGCTG GCCGGCCCGAACTGGAATCTTCCTCTCCCTGGGGCTCCTTCTCTTGGGCCTTTGTTTCTGAGCTG A G ADGRD1 Ensembl:ENSG00000111452 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131014372..131014501 26863196 MeRIP-seq:(Medium) rs1410198109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83423,RMVar_hsa_circ_92728,RMVar_hsa_circ_161723,RMVar_hsa_circ_161724,RMVar_hsa_circ_356704,RMVar_hsa_circ_88489,RMVar_hsa_circ_67772,RMVar_hsa_circ_124096,RMVar_hsa_circ_161727,RMVar_hsa_circ_161728,RMVar_hsa_circ_56593 96218 RMVar_ID_96218 Human_SNP_ID_520926105 m1A Human chr12 - 131034229 131034229 131034229 CGCAGAGCAAGGCAGACGCATGGCGGGAGCGGAGTGGAATGGGCGGGGAGTGGCCCAGAGTGCGG CGCAGAGCAAGGCAGACGCATGGCGGGAGCGGGGTGGAATGGGCGGGGAGTGGCCCAGAGTGCGG T C AC078925.1 Ensembl:ENSG00000256810 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131034181..131034456 26863196 MeRIP-seq:(Medium) rs904261773 Functional Loss SNV dbSNP153 33..33 33 - - - 96219 RMVar_ID_96219 Human_SNP_ID_520950795 m1A Human chr12 - 131129140 131129140 131129140 CACTCACACTCAGACAGCAGGGCGGGCCTGTCACTCACACCCAGACAGCAGGGCCGGCCTGTCAC CACTCACACTCAGACAGCAGGGCGGGCCTGTCTCTCACACCCAGACAGCAGGGCCGGCCTGTCAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131129109..131129214 26863196 MeRIP-seq:(Medium) rs1310675901 Functional Loss SNV dbSNP153 33..33 33 - - - 96220 RMVar_ID_96220 Human_SNP_ID_520950885 m1A Human chr12 - 131129364 131129333 131129364 GGGCCTGTCACTCACACCCAGACAGGAGGGCCAGCCTGTCACTCACACCCAGACAGGAGGGCAGG GGGCCTGTCACTCACACCCAGACAGGAGGGCC_______________________________GG CTGCCCTCCTGTCTGGGTGTGAGTGACAGGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131129317..131129538 26863196 MeRIP-seq:(Medium) rs1566136584 Functional Loss DEL dbSNP153 33..63 33 - - - 96221 RMVar_ID_96221 Human_SNP_ID_520950886 m1A Human chr12 - 131129364 131129334 131129365 GGGCCTGTCACTCACACCCAGACAGGAGGGCCAGCCTGTCACTCACACCCAGACAGGAGGGCAGG GGGCCTGTCACTCACACCCAGACAGGAGGGC_______________________________AGG TGCCCTCCTGTCTGGGTGTGAGTGACAGGCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131129317..131129538 26863196 MeRIP-seq:(Medium) rs1566136593 Functional Loss DEL dbSNP153 32..62 33 - - - 96222 RMVar_ID_96222 Human_SNP_ID_520950889 m1A Human chr12 - 131129364 131129336 131129365 GGGCCTGTCACTCACACCCAGACAGGAGGGCCAGCCTGTCACTCACACCCAGACAGGAGGGCAGG GGGCCTGTCACTCACACCCAGACAGGAGGGC_____________________________GCAGG CCCTCCTGTCTGGGTGTGAGTGACAGGCTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131129317..131129538 26863196 MeRIP-seq:(Medium) rs1231566104 Functional Loss DEL dbSNP153 32..60 33 - - - 96223 RMVar_ID_96223 Human_SNP_ID_520950896 m1A Human chr12 - 131129364 131129364 131129364 GGGCCTGTCACTCACACCCAGACAGGAGGGCCAGCCTGTCACTCACACCCAGACAGGAGGGCAGG GGGCCTGTCACTCACACCCAGACAGGAGGGCCGGCCTGTCACTCACACCCAGACAGGAGGGCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131129317..131129538 26863196 MeRIP-seq:(Medium) rs1211733 Functional Loss SNV dbSNP153 33..33 33 - - - 96224 RMVar_ID_96224 Human_SNP_ID_520977249 m1A Human chr12 - 131231856 131231854 131231857 GAGGAGGAGGGGAGGAAGAGGGGAGGATGAGGAGAAGAGGAGGAAGAGGAGGAGGAGAAGGAGGA GAGGAGGAGGGGAGGAAGAGGGGAGGATGAG___AAGAGGAGGAAGAGGAGGAGGAGAAGGAGGA TCTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131231807..131231892 26863196 MeRIP-seq:(Medium) rs1290029739 Functional Loss DEL dbSNP153 32..34 33 - - - 96225 RMVar_ID_96225 Human_SNP_ID_521022742 m1A Human chr12 + 131395654 131395635 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATG___________________TGGTGATGGTGATGGTGATGATGGTGATGGTG GGTGATGATGGTGATGATGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs1566220355 Functional Loss DEL dbSNP153 15..33 33 - - - 96226 RMVar_ID_96226 Human_SNP_ID_521022751 m1A Human chr12 + 131395654 131395645 131395655 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGG__________GGTGATGGTGATGGTGATGATGGTGATGGTG GTGATGATGAT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs1566220385 Functional Loss DEL dbSNP153 25..34 33 - - - 96227 RMVar_ID_96227 Human_SNP_ID_521022753 m1A Human chr12 + 131395654 131395645 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGG_________TGGTGATGGTGATGGTGATGATGGTGATGGTG GTGATGATGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs149287960 Functional Loss DEL dbSNP153 25..33 33 - - - 96228 RMVar_ID_96228 Human_SNP_ID_521022754 m1A Human chr12 + 131395654 131395645 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGGTGA______TGGTGATGGTGATGGTGATGATGGTGATGGTG GTGATGATGA GTGA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs149287960 Functional Loss DEL dbSNP153 28..33 33 - - - 96229 RMVar_ID_96229 Human_SNP_ID_521022755 m1A Human chr12 + 131395654 131395645 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGGTGATGA___TGGTGATGGTGATGGTGATGATGGTGATGGTG GTGATGATGA GTGATGA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs149287960 Functional Loss DEL dbSNP153 31..33 33 - - - 96230 RMVar_ID_96230 Human_SNP_ID_521022766 m1A Human chr12 + 131395654 131395654 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGGTGATGATGGTGGTGATGGTGATGGTGATGATGGTGATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs142796441 Functional Loss SNV dbSNP153 33..33 33 - - - 96231 RMVar_ID_96231 Human_SNP_ID_521022847 m1A Human chr12 + 131395765 131395761 131395765 TGGTGATGGTGATGGTGATGATGGTGATGATGATGATGGTGATGATGATGGTGATGGTGATGGTG TGGTGATGGTGATGGTGATGATGGTGATG____TGATGGTGATGATGATGGTGATGGTGATGGTG GATGA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131395715..131395819 26863196 MeRIP-seq:(Medium) rs1463460104 Functional Loss DEL dbSNP153 30..33 33 - - - 96232 RMVar_ID_96232 Human_SNP_ID_521022850 m1A Human chr12 + 131395765 131395765 131395765 TGGTGATGGTGATGGTGATGATGGTGATGATGATGATGGTGATGATGATGGTGATGGTGATGGTG TGGTGATGGTGATGGTGATGATGGTGATGATGGTGATGGTGATGATGATGGTGATGGTGATGGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131395715..131395819 26863196 MeRIP-seq:(Medium) rs1029257918 Functional Loss SNV dbSNP153 33..33 33 - - - 96233 RMVar_ID_96233 Human_SNP_ID_521058685 m1A Human chr12 + 131539468 131539468 131539468 TGGTGATGGTGATGATGATGGTAATGGTGATGATGATGGTGATGGTGATGATGGTGATGGTGATG TGGTGATGGTGATGATGATGGTAATGGTGATGGTGATGGTGATGGTGATGATGGTGATGGTGATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131539436..131539530 26863196 MeRIP-seq:(Medium) rs61934630 Functional Loss SNV dbSNP153 33..33 33 - - - 96234 RMVar_ID_96234 Human_SNP_ID_521108038 m1A Human chr12 + 131711181 131711181 131711181 CTGAAGGGGTAGGCCAAGTGGAGGTATCAGGGACGTCGCGCGGCACAGAAGAGGACCAGCCTGGA CTGAAGGGGTAGGCCAAGTGGAGGTATCAGGGGCGTCGCGCGGCACAGAAGAGGACCAGCCTGGA A G SFSWAP Ensembl:ENSG00000061936 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:131711101..131711274 26863196 MeRIP-seq:(Medium) rs1225423856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36371,Human_RBP_ID_229668,Human_RBP_ID_810082,Human_RBP_ID_3942454,Human_RBP_ID_4247152,Human_RBP_ID_5350453,Human_RBP_ID_6152921,Human_RBP_ID_11875956,Human_RBP_ID_18417364,Human_RBP_ID_22039732,Human_RBP_ID_22436175,Human_RBP_ID_22910655,Human_RBP_ID_23118068,Human_RBP_ID_24543511,Human_RBP_ID_26322370 96235 RMVar_ID_96235 Human_SNP_ID_521108124 m1A Human chr12 + 131711375 131711375 131711375 CGGCTATGCCTGCAAGCTGTTCCGGGACGACGAGCGGGCCCTGGCTCAGGAACAGGGACAGCACC CGGCTATGCCTGCAAGCTGTTCCGGGACGACGGGCGGGCCCTGGCTCAGGAACAGGGACAGCACC A G SFSWAP Ensembl:ENSG00000061936 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:131711326..131711927 32194978 MeRIP-seq:(Medium) rs556358427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_36372,Human_RBP_ID_1065548,Human_RBP_ID_3942455,Human_RBP_ID_9365844,Human_RBP_ID_11875961,Human_RBP_ID_22039733,Human_RBP_ID_22910929,Human_RBP_ID_26322372,Human_RBP_ID_27806255 Human_Splice_Rec_1445219,Human_Splice_Rec_1445253,Human_Splice_Rec_1445281,Human_Splice_Rec_1445305 96236 RMVar_ID_96236 Human_SNP_ID_521108962 m1A Human chr12 + 131714777 131714774 131714778 CTACAACTTTAGAAATATATAAAGTTTTTCTCAGTAATTTTCTATTTTTGTTGATAAAATTCTCA CTACAACTTTAGAAATATATAAAGTTTTTC____TAATTTTCTATTTTTGTTGATAAAATTCTCA CTCAG C SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131714773..131715006 26863196 MeRIP-seq:(Medium) rs1565999402 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_2313561,Human_RBP_ID_22645619 RMVar_hsa_circ_63354,RMVar_hsa_circ_367351,RMVar_hsa_circ_309913,RMVar_hsa_circ_51181,RMVar_hsa_circ_161730,RMVar_hsa_circ_161731 96237 RMVar_ID_96237 Human_SNP_ID_521108968 m1A Human chr12 + 131714788 131714788 131714788 GAAATATATAAAGTTTTTCTCAGTAATTTTCTATTTTTGTTGATAAAATTCTCATTTTTATTCAA GAAATATATAAAGTTTTTCTCAGTAATTTTCTGTTTTTGTTGATAAAATTCTCATTTTTATTCAA A G SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131714786..131714989 26863196 MeRIP-seq:(Medium) rs898449261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2313561,Human_RBP_ID_22645619 RMVar_hsa_circ_63354,RMVar_hsa_circ_367351,RMVar_hsa_circ_309913,RMVar_hsa_circ_51181,RMVar_hsa_circ_161730,RMVar_hsa_circ_161731 96238 RMVar_ID_96238 Human_SNP_ID_521118810 m1A Human chr12 - 131753211 131753211 131753211 GTCACGCCAGCAGGAAGGGTGCTGTAGTAAGTAGTCACGTCGATTCCGGGAGGGGGCGGCGCCAG GTCACGCCAGCAGGAAGGGTGCTGTAGTAAGTGGTCACGTCGATTCCGGGAGGGGGCGGCGCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131753162..131753402 26863196 MeRIP-seq:(Medium) rs1449078998 Functional Loss SNV dbSNP153 33..33 33 - - - 96239 RMVar_ID_96239 Human_SNP_ID_521119253 m1A Human chr12 + 131754474 131754474 131754474 ATGTCGCCAGGAACGGCCTGAAGTTCGAGACCAGTGTTCGTGCCAAGAATGATCAAAGGTCAGAA ATGTCGCCAGGAACGGCCTGAAGTTCGAGACCGGTGTTCGTGCCAAGAATGATCAAAGGTCAGAA A G SFSWAP Ensembl:ENSG00000061936 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131754328..131754500 26863196 MeRIP-seq:(Medium) rs1376530299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33202,Human_RBP_ID_415074,Human_RBP_ID_1480064,Human_RBP_ID_1790638,Human_RBP_ID_11876939,Human_RBP_ID_26322380,Human_RBP_ID_27806261 Human_Splice_Rec_1445235,Human_Splice_Rec_1445269,Human_Splice_Rec_1445295,Human_Splice_Rec_1445321,Human_Splice_Rec_1445351 RMVar_hsa_circ_51181,RMVar_hsa_circ_6093,RMVar_hsa_circ_50163,RMVar_hsa_circ_52589,RMVar_hsa_circ_49579,RMVar_hsa_circ_161737,RMVar_hsa_circ_161739,RMVar_hsa_circ_293726,RMVar_hsa_circ_375465,RMVar_hsa_circ_284835,RMVar_hsa_circ_161738 96240 RMVar_ID_96240 Human_SNP_ID_521122466 m1A Human chr12 + 131766197 131766197 131766197 CTGGCCCAGGCGTCTAAGGAGTCAAAAGAGAAACAGCTTCAAGCAGAACGTAAAAGGAAAGCGGC CTGGCCCAGGCGTCTAAGGAGTCAAAAGAGAAGCAGCTTCAAGCAGAACGTAAAAGGAAAGCGGC A G SFSWAP Ensembl:ENSG00000061936 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131766090..131766196 26863196 MeRIP-seq:(Medium) rs145970901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33205,Human_RBP_ID_11877085 Human_Splice_Rec_1445242,Human_Splice_Rec_1445276,Human_Splice_Rec_1445302,Human_Splice_Rec_1445328,Human_Splice_Rec_1445356 RMVar_hsa_circ_51181,RMVar_hsa_circ_50163,RMVar_hsa_circ_52589,RMVar_hsa_circ_49579,RMVar_hsa_circ_33101,RMVar_hsa_circ_161739,RMVar_hsa_circ_293726,RMVar_hsa_circ_375465,RMVar_hsa_circ_161738,RMVar_hsa_circ_161740,RMVar_hsa_circ_318889,RMVar_hsa_circ_360958,RMVar_hsa_circ_322754,RMVar_hsa_circ_161741 96241 RMVar_ID_96241 Human_SNP_ID_521125949 m1A Human chr12 - 131779232 131779232 131779232 ACTCACCCGCGCCGCCCTCTTCACACACGCTCACCCGCGCCGCCCTCTTCACACACACTCATCCG ACTCACCCGCGCCGCCCTCTTCACACACGCTCGCCCGCGCCGCCCTCTTCACACACACTCATCCG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131779129..131779362 26863196 MeRIP-seq:(Medium) rs1278744351 Functional Loss SNV dbSNP153 33..33 33 - - - 96242 RMVar_ID_96242 Human_SNP_ID_521125968 m1A Human chr12 + 131779244 131779244 131779244 TGTGAAGAGGGCGGCGCGGGTGAGCGTGTGTGAAGAGGGCGGCGCGGGTGAGTGTGTGTGAAGAG TGTGAAGAGGGCGGCGCGGGTGAGCGTGTGTGCAGAGGGCGGCGCGGGTGAGTGTGTGTGAAGAG A C SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131779140..131779364 26863196 MeRIP-seq:(Medium) rs1277657462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5645102,Human_RBP_ID_8177638,Human_RBP_ID_18934892,Human_RBP_ID_23113454,Human_RBP_ID_23547790,Human_RBP_ID_26777596 RMVar_hsa_circ_50163,RMVar_hsa_circ_33101,RMVar_hsa_circ_161739,RMVar_hsa_circ_375465,RMVar_hsa_circ_360958,RMVar_hsa_circ_352864 96243 RMVar_ID_96243 Human_SNP_ID_521131548 m1A Human chr12 + 131799058 131799058 131799058 CTCTGCATTAGGGGAGTCTCTCAGGAAAAAGAAGCCCAGATCTCTTCAGCAATCGTTTCTTCCGT CTCTGCATTAGGGGAGTCTCTCAGGAAAAAGAGGCCCAGATCTCTTCAGCAATCGTTTCTTCCGT A G SFSWAP Ensembl:ENSG00000061936 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:131797199..131799076 32194978 MeRIP-seq:(Medium) rs780764619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1445250,Human_Splice_Rec_1445251,Human_Splice_Rec_1445338,Human_Splice_Rec_1445339,Human_Splice_Rec_1445364,Human_Splice_Rec_1445365,Human_Splice_Rec_1445368,Human_Splice_Rec_1445369 96244 RMVar_ID_96244 Human_SNP_ID_521132512 m1A Human chr12 - 131801683 131801683 131801683 CACGAACAGCCACGGCAAACACGGGCCACGGCAAAGACGAGCCACGGCAAACATGAGCCACAGCA CACGAACAGCCACGGCAAACACGGGCCACGGCGAAGACGAGCCACGGCAAACATGAGCCACAGCA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131801637..131801792 26863196 MeRIP-seq:(Medium) rs1182407261 Functional Loss SNV dbSNP153 33..33 33 - - - 96245 RMVar_ID_96245 Human_SNP_ID_521139851 m1A Human chr12 + 131828489 131828489 131828489 GGGACCCTGCACGCCGCCCGCGGGCCCATGTGAGCGCCATGCGGCGCCGCGCAGCCCGGGGACCC GGGACCCTGCACGCCGCCCGCGGGCCCATGTGGGCGCCATGCGGCGCCGCGCAGCCCGGGGACCC A G MMP17 Ensembl:ENSG00000198598 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131828452..131828558 26863196 MeRIP-seq:(Medium) rs889715660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9322868 96246 RMVar_ID_96246 Human_SNP_ID_521140984 m1A Human chr12 - 131831893 131831893 131831893 TCCCCCTTCCCATCTCCCCCCAGATCCTCTCCAGCCTTCCCCCTTCCGGTCCCCCCACGCCGATC TCCCCCTTCCCATCTCCCCCCAGATCCTCTCCCGCCTTCCCCCTTCCGGTCCCCCCACGCCGATC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131831889..131831995 26863196 MeRIP-seq:(Medium) rs1566080722 Functional Loss SNV dbSNP153 33..33 33 - - - 96247 RMVar_ID_96247 Human_SNP_ID_521143033 m1A Human chr12 - 131838577 131838577 131838577 GCAGGGAAAGCATGGAGCTCAGAGCCTAGCCCAGCTCACTCCCCACCCTAGGATCCCGAGCATCC GCAGGGAAAGCATGGAGCTCAGAGCCTAGCCCTGCTCACTCCCCACCCTAGGATCCCGAGCATCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131838572..131838957 26863196 MeRIP-seq:(Medium) rs200638152 Functional Loss SNV dbSNP153 33..33 33 - - - 96248 RMVar_ID_96248 Human_SNP_ID_521143034 m1A Human chr12 - 131838577 131838577 131838577 GCAGGGAAAGCATGGAGCTCAGAGCCTAGCCCAGCTCACTCCCCACCCTAGGATCCCGAGCATCC GCAGGGAAAGCATGGAGCTCAGAGCCTAGCCCGGCTCACTCCCCACCCTAGGATCCCGAGCATCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131838572..131838957 26863196 MeRIP-seq:(Medium) rs200638152 Functional Loss SNV dbSNP153 33..33 33 - - - 96249 RMVar_ID_96249 Human_SNP_ID_521147592 m1A Human chr12 + 131851608 131851608 131851608 GCTGGGGGCCCACCCCTCTCTGTGCCGGCGCCACCAACCCCACCCACACTGCTGCCTGGTGCTCC GCTGGGGGCCCACCCCTCTCTGTGCCGGCGCCGCCAACCCCACCCACACTGCTGCCTGGTGCTCC A G MMP17 Ensembl:ENSG00000198598 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131851557..131851717 26863196 MeRIP-seq:(Medium) rs1295173137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9013469 96250 RMVar_ID_96250 Human_SNP_ID_521149603 m1A Human chr12 - 131857754 131857752 131857755 CCCAGCACCTCCTCACAGCACCCACCACCACCACAGAGCACCCACCACTGCCCCAGAGCACCCAG CCCAGCACCTCCTCACAGCACCCACCACCAC___AGAGCACCCACCACTGCCCCAGAGCACCCAG TGTG T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131857647..131857857 26863196 MeRIP-seq:(Medium) rs1160904926 Functional Loss DEL dbSNP153 32..34 33 - - - 96251 RMVar_ID_96251 Human_SNP_ID_521149604 m1A Human chr12 - 131857754 131857753 131857754 CCCAGCACCTCCTCACAGCACCCACCACCACCACAGAGCACCCACCACTGCCCCAGAGCACCCAG CCCAGCACCTCCTCACAGCACCCACCACCACC_CAGAGCACCCACCACTGCCCCAGAGCACCCAG GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131857647..131857857 26863196 MeRIP-seq:(Medium) rs1416230554 Functional Loss DEL dbSNP153 33..33 33 - - - 96252 RMVar_ID_96252 Human_SNP_ID_521159975 m1A Human chr12 + 131894968 131894968 131894968 CTCCGCCTGAGTCCCCCGCGCCTTGGCCCGCCACCCCCCGCCCCGCGCCCCCGGCCCGCCTGCGC CTCCGCCTGAGTCCCCCGCGCCTTGGCCCGCCCCCCCCCGCCCCGCGCCCCCGGCCCGCCTGCGC A C ULK1 Ensembl:ENSG00000177169 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr12:131894651..131895100;chr12:131894885..131894979 26863196,26863410 MeRIP-seq:(Medium) rs1467109018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_870930,Human_miRNA_ID_885200 96253 RMVar_ID_96253 Human_SNP_ID_521159976 m1A Human chr12 + 131894968 131894968 131894968 CTCCGCCTGAGTCCCCCGCGCCTTGGCCCGCCACCCCCCGCCCCGCGCCCCCGGCCCGCCTGCGC CTCCGCCTGAGTCCCCCGCGCCTTGGCCCGCCGCCCCCCGCCCCGCGCCCCCGGCCCGCCTGCGC A G ULK1 Ensembl:ENSG00000177169 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr12:131894651..131895100;chr12:131894885..131894979 26863196,26863410 MeRIP-seq:(Medium) rs1467109018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_870930,Human_miRNA_ID_885200 96254 RMVar_ID_96254 Human_SNP_ID_521160132 m1A Human chr12 + 131895334 131895334 131895334 GCCCCGAGATCCGCTGCCGGGCTTTCCAGCCCAGATCCTCACTCCGAGACCCCCAGCCCGACTTT GCCCCGAGATCCGCTGCCGGGCTTTCCAGCCCGGATCCTCACTCCGAGACCCCCAGCCCGACTTT A G ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131895329..131895413 26863196 MeRIP-seq:(Medium) rs7960223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5126979,Human_RBP_ID_17074985 96255 RMVar_ID_96255 Human_SNP_ID_521160465 m1A Human chr12 - 131896270 131896270 131896270 GCCGCCTGTGCCCCGGCCCGGCCCTGACTGCCAGCGAGCAGGAGTCTCCGGCGGCCCCTCCCCCG GCCGCCTGTGCCCCGGCCCGGCCCTGACTGCCGGCGAGCAGGAGTCTCCGGCGGCCCCTCCCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131896268..131896396 26863196 MeRIP-seq:(Medium) rs1211863849 Functional Loss SNV dbSNP153 33..33 33 - - - 96256 RMVar_ID_96256 Human_SNP_ID_521161725 m1A Human chr12 - 131900756 131900756 131900756 GCAGGGCTGGACACCTCTTGACTCAGGTCTCCACTGCAAGTAACTCACAGGCAGCGGCTCTGTCT GCAGGGCTGGACACCTCTTGACTCAGGTCTCCGCTGCAAGTAACTCACAGGCAGCGGCTCTGTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131900753..131900958 26863196 MeRIP-seq:(Medium) rs146775673 Functional Loss SNV dbSNP153 33..33 33 - - - 96257 RMVar_ID_96257 Human_SNP_ID_521161736 m1A Human chr12 - 131900790 131900790 131900790 GACTGCCTGGACCCATGGTCTCCCAGGACCCCAAGCAGGGCTGGACACCTCTTGACTCAGGTCTC GACTGCCTGGACCCATGGTCTCCCAGGACCCCGAGCAGGGCTGGACACCTCTTGACTCAGGTCTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131900675..131900922 26863196 MeRIP-seq:(Medium) rs769146152 Functional Loss SNV dbSNP153 33..33 33 - - - 96258 RMVar_ID_96258 Human_SNP_ID_521161921 m1A Human chr12 + 131901424 131901423 131901424 TACTGGAAAGTGCAAAACAGATGAGAAGATATACCACAACAGGCCCTGTGTGGCGTAGCAAGCGC TACTGGAAAGTGCAAAACAGATGAGAAGATAT_CCACAACAGGCCCTGTGTGGCGTAGCAAGCGC TA T ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131901422..131901498 26863196 MeRIP-seq:(Medium) rs1248772238 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_27625099 96259 RMVar_ID_96259 Human_SNP_ID_521164576 m1A Human chr12 + 131909832 131909832 131909832 TGTTCTACGAGAAGAACAAGACGTTGGTCCCCACGTAAGCACCCTCCCGCCTTCCCTTCCCTTCC TGTTCTACGAGAAGAACAAGACGTTGGTCCCCGCGTAAGCACCCTCCCGCCTTCCCTTCCCTTCC A G ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131909819..131909920 26863196 MeRIP-seq:(Medium) rs764646120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3943894 Human_Splice_Rec_1445476,Human_Splice_Rec_1445477,Human_Splice_Rec_1445524,Human_Splice_Rec_1445525 RMVar_hsa_circ_41107 96260 RMVar_ID_96260 Human_SNP_ID_521164670 m1A Human chr12 + 131909951 131909951 131909951 CATCCCCCGGGAGACCTCGGCCCCGCTGCGGCAGCTGCTCCTGGCCCTACTGCAACGCAACCACA CATCCCCCGGGAGACCTCGGCCCCGCTGCGGCGGCTGCTCCTGGCCCTACTGCAACGCAACCACA A G ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr12:131909815..131910033;chr12:131909185..131912025 26863196 MeRIP-seq:(Medium) rs761167009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230145,Human_RBP_ID_3942474,Human_RBP_ID_5347051,Human_RBP_ID_19057197,Human_RBP_ID_25016622 Human_Splice_Rec_1445478,Human_Splice_Rec_1445479,Human_Splice_Rec_1445526 RMVar_hsa_circ_41107,RMVar_hsa_circ_43272 96261 RMVar_ID_96261 Human_SNP_ID_521164678 m1A Human chr12 + 131909973 131909973 131909973 CCGCTGCGGCAGCTGCTCCTGGCCCTACTGCAACGCAACCACAAGGACCGCATGGACTTCGGTGA CCGCTGCGGCAGCTGCTCCTGGCCCTACTGCAGCGCAACCACAAGGACCGCATGGACTTCGGTGA A G ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:131909848..131910025 26863196 MeRIP-seq:(Medium) rs143247728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1445478,Human_Splice_Rec_1445479,Human_Splice_Rec_1445526 RMVar_hsa_circ_41107,RMVar_hsa_circ_43272 96262 RMVar_ID_96262 Human_SNP_ID_521164802 m1A Human chr12 + 131910266 131910266 131910266 ACTCCTCCTTCCTCCTGCAGATGAGTTTTTTCATCACCCTTTCCTCGATGCCAGCCCCTCGGTCA ACTCCTCCTTCCTCCTGCAGATGAGTTTTTTCGTCACCCTTTCCTCGATGCCAGCCCCTCGGTCA A G ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:131910251..131910300 26863196 MeRIP-seq:(Medium) rs773116004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942475,Human_RBP_ID_9013493,Human_RBP_ID_9277511,Human_RBP_ID_17353009,Human_RBP_ID_22436177 Human_Splice_Rec_1445480,Human_Splice_Rec_1445481 RMVar_hsa_circ_41107 96263 RMVar_ID_96263 Human_SNP_ID_521164937 m1A Human chr12 + 131910716 131910716 131910716 CAGACTGACCTATGCATGTTTATCTCAGCCCCACCCGTGCCTGTGCCCTCGTACCCAAGCTCGGG CAGACTGACCTATGCATGTTTATCTCAGCCCCCCCCGTGCCTGTGCCCTCGTACCCAAGCTCGGG A C ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131910231..131912126 26863196 MeRIP-seq:(Medium) rs1474795565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942476,Human_RBP_ID_18976478 Human_Splice_Rec_1445482,Human_Splice_Rec_1445483 Human_miRNA_ID_1372814,Human_miRNA_ID_2491548 RMVar_hsa_circ_41107,RMVar_hsa_circ_93798,RMVar_hsa_circ_339888,RMVar_hsa_circ_161746 96264 RMVar_ID_96264 Human_SNP_ID_521166102 m1A Human chr12 + 131914026 131914026 131914026 GCAGAAGGGACTATAGTGGGAGGAGCATTGACAGGAGTAGGTGAATGAGGAAACCAACCAGGGAC GCAGAAGGGACTATAGTGGGAGGAGCATTGACGGGAGTAGGTGAATGAGGAAACCAACCAGGGAC A G ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131914024..131914397 26863196 MeRIP-seq:(Medium) rs538577758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260002,Human_RBP_ID_5172845,Human_RBP_ID_9344409,Human_RBP_ID_19061761,Human_RBP_ID_27807458 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746 96265 RMVar_ID_96265 Human_SNP_ID_521166833 m1A Human chr12 + 131915995 131915995 131915995 CTGACTTGCACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCACGGACCCCCTGGGAGCTGTGTTC CTGACTTGCACGTCGTCCGCCCCAAGCTGCCCGAACCCCCCACGGACCCCCTGGGAGCTGTGTTC A G ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:131915126..131916175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5491222,Human_RBP_ID_27806267 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746,RMVar_hsa_circ_161747,RMVar_hsa_circ_82030,RMVar_hsa_circ_9023 96266 RMVar_ID_96266 Human_SNP_ID_521166834 m1A Human chr12 + 131915997 131915997 131915997 GACTTGCACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCACGGACCCCCTGGGAGCTGTGTTCAG GACTTGCACGTCGTCCGCCCCAAGCTGCCCAACCCCCCCACGGACCCCCTGGGAGCTGTGTTCAG A C ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131915875..131916190 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5491222,Human_RBP_ID_27806267 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746,RMVar_hsa_circ_161747,RMVar_hsa_circ_82030,RMVar_hsa_circ_9023 96267 RMVar_ID_96267 Human_SNP_ID_521166844 m1A Human chr12 + 131916004 131916004 131916004 ACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCACGGACCCCCTGGGAGCTGTGTTCAGCCCACCA ACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCCCGGACCCCCTGGGAGCTGTGTTCAGCCCACCA A C ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:131915876..131916195;chr12:131915924..131916175 26863196 MeRIP-seq:(Medium) rs1176637341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5491222,Human_RBP_ID_27806267 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746,RMVar_hsa_circ_161747,RMVar_hsa_circ_82030,RMVar_hsa_circ_9023 96268 RMVar_ID_96268 Human_SNP_ID_521166852 m1A Human chr12 - 131916014 131916014 131916014 GGCTGGCCTGTGGTGGGCTGAACACAGCTCCCAGGGGGTCCGTGGGGGGTTTGGGCAGCTTGGGG GGCTGGCCTGTGGTGGGCTGAACACAGCTCCCGGGGGGTCCGTGGGGGGTTTGGGCAGCTTGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:131915876..131916181;chr12:131915851..131916225 26863196 MeRIP-seq:(Medium) rs775884176 Functional Loss SNV dbSNP153 33..33 33 - - - 96269 RMVar_ID_96269 Human_SNP_ID_521166888 m1A Human chr12 - 131916086 131916086 131916086 GCAGGAAGTCGGGCAGCTTGGGTGAGCCCCGCAGGTTCCGGCAGGACTGCAGGCCGTGGGACGGC GCAGGAAGTCGGGCAGCTTGGGTGAGCCCCGCGGGTTCCGGCAGGACTGCAGGCCGTGGGACGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:131916039..131916197 32194978 MeRIP-seq:(Medium) rs749074811 Functional Loss SNV dbSNP153 33..33 33 - - - 96270 RMVar_ID_96270 Human_SNP_ID_521167018 m1A Human chr12 - 131916374 131916374 131916374 GGGCACAGCCTAGGAGGACAGAGATGGGGTGAAGACTGCCCCGCAGGTCTGCAGCCCTGGGGCCC GGGCACAGCCTAGGAGGACAGAGATGGGGTGATGACTGCCCCGCAGGTCTGCAGCCCTGGGGCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131916371..131916527 26863196 MeRIP-seq:(Medium) rs1408239498 Functional Loss SNV dbSNP153 33..33 33 - - - 96271 RMVar_ID_96271 Human_SNP_ID_521167019 m1A Human chr12 - 131916374 131916374 131916374 GGGCACAGCCTAGGAGGACAGAGATGGGGTGAAGACTGCCCCGCAGGTCTGCAGCCCTGGGGCCC GGGCACAGCCTAGGAGGACAGAGATGGGGTGAGGACTGCCCCGCAGGTCTGCAGCCCTGGGGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131916371..131916527 26863196 MeRIP-seq:(Medium) rs1408239498 Functional Loss SNV dbSNP153 33..33 33 - - - 96272 RMVar_ID_96272 Human_SNP_ID_521167739 m1A Human chr12 + 131917253 131917253 131917253 AGGCTGTGGGACGGGGGTCGGGTTCGGCTCGGAGGCTGTGGGACGGGGGTCGGGTTCGGCTCGGA AGGCTGTGGGACGGGGGTCGGGTTCGGCTCGGGGGCTGTGGGACGGGGGTCGGGTTCGGCTCGGA A G ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:131916979..131917507;chr12:131917247..131917445;chr12:131917043..131917445 26863196 MeRIP-seq:(Medium) rs1418952589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260006,Human_RBP_ID_754339,Human_RBP_ID_811136,Human_RBP_ID_3418720,Human_RBP_ID_3942485,Human_RBP_ID_5235574,Human_RBP_ID_5314757,Human_RBP_ID_8070580,Human_RBP_ID_8177651,Human_RBP_ID_8229683,Human_RBP_ID_8725440,Human_RBP_ID_8940748,Human_RBP_ID_9416015,Human_RBP_ID_17186484,Human_RBP_ID_17357456,Human_RBP_ID_18934895,Human_RBP_ID_19057209,Human_RBP_ID_21967268,Human_RBP_ID_22709992,Human_RBP_ID_23118071,Human_RBP_ID_24408225,Human_RBP_ID_26776966 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746,RMVar_hsa_circ_161747,RMVar_hsa_circ_82030 96273 RMVar_ID_96273 Human_SNP_ID_521167757 m1A Human chr12 - 131917275 131917275 131917275 CCCCAACCCCCGTCCCACAGCCTCCGAGCCGAACCCGACCCCCGTCCCACAGCCTCCGAGCCGAA CCCCAACCCCCGTCCCACAGCCTCCGAGCCGATCCCGACCCCCGTCCCACAGCCTCCGAGCCGAA T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131917073..131917440 26863196 MeRIP-seq:(Medium) rs1354665707 Functional Loss SNV dbSNP153 33..33 33 - - - 96274 RMVar_ID_96274 Human_SNP_ID_521167758 m1A Human chr12 - 131917275 131917275 131917275 CCCCAACCCCCGTCCCACAGCCTCCGAGCCGAACCCGACCCCCGTCCCACAGCCTCCGAGCCGAA CCCCAACCCCCGTCCCACAGCCTCCGAGCCGACCCCGACCCCCGTCCCACAGCCTCCGAGCCGAA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131917073..131917440 26863196 MeRIP-seq:(Medium) rs1354665707 Functional Loss SNV dbSNP153 33..33 33 - - - 96275 RMVar_ID_96275 Human_SNP_ID_521168429 m1A Human chr12 - 131918601 131918601 131918601 CCCCTCCAGGTTCGCAGTAATGGGGTCGGCAAAGCTGCAGCCGTGTCCTGGAGCAGGGAGCTCAG CCCCTCCAGGTTCGCAGTAATGGGGTCGGCAAGGCTGCAGCCGTGTCCTGGAGCAGGGAGCTCAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:131918551..131918700 26863196 MeRIP-seq:(Medium) rs1419316815 Functional Loss SNV dbSNP153 33..33 33 - - - 96276 RMVar_ID_96276 Human_SNP_ID_521168449 m1A Human chr12 - 131918626 131918626 131918626 GGTCGGGGGCCTCGAAGGTCACAGCCCCCTCCAGGTTCGCAGTAATGGGGTCGGCAAAGCTGCAG GGTCGGGGGCCTCGAAGGTCACAGCCCCCTCCGGGTTCGCAGTAATGGGGTCGGCAAAGCTGCAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:131918576..131918625 26863196 MeRIP-seq:(Medium) rs909496996 Functional Loss SNV dbSNP153 33..33 33 - - - 96277 RMVar_ID_96277 Human_SNP_ID_521168450 m1A Human chr12 - 131918626 131918626 131918626 GGTCGGGGGCCTCGAAGGTCACAGCCCCCTCCAGGTTCGCAGTAATGGGGTCGGCAAAGCTGCAG GGTCGGGGGCCTCGAAGGTCACAGCCCCCTCCCGGTTCGCAGTAATGGGGTCGGCAAAGCTGCAG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:131918576..131918625 26863196 MeRIP-seq:(Medium) rs909496996 Functional Loss SNV dbSNP153 33..33 33 - - - 96278 RMVar_ID_96278 Human_SNP_ID_521168646 m1A Human chr12 + 131918969 131918845 131918969 GCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCAGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA _________________________________GGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA CGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGTAGGGTGTGGGGTGTAGGGTGTGTGGGGTGCAGGGTGTGTGGGGTGCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCA C ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131918940..131919203 26863196 MeRIP-seq:(Medium) rs1566129086 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_3420944,Human_RBP_ID_5171580,Human_RBP_ID_5645109,Human_RBP_ID_8071205,Human_RBP_ID_8178861,Human_RBP_ID_8229690,Human_RBP_ID_9416686,Human_RBP_ID_21967274 RMVar_hsa_circ_161747,RMVar_hsa_circ_82030 96279 RMVar_ID_96279 Human_SNP_ID_521168772 m1A Human chr12 + 131918969 131918969 131918969 GCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCAGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA GCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCCGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA A C ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131918940..131919203 26863196 MeRIP-seq:(Medium) rs1209532701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3420944,Human_RBP_ID_5171580,Human_RBP_ID_5645109,Human_RBP_ID_8071205,Human_RBP_ID_8178861,Human_RBP_ID_8229690,Human_RBP_ID_9416686,Human_RBP_ID_21967274 RMVar_hsa_circ_161747,RMVar_hsa_circ_82030 96280 RMVar_ID_96280 Human_SNP_ID_521168773 m1A Human chr12 + 131918969 131918969 131918969 GCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCAGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA GCAGGGTGTGTGGGGTGCAGGGTGTGGGGTGCGGGGTGTGTGGGGTGTCGGGTGTGTGGGGTGCA A G ULK1 Ensembl:ENSG00000177169 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131918940..131919203 26863196 MeRIP-seq:(Medium) rs1209532701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3420944,Human_RBP_ID_5171580,Human_RBP_ID_5645109,Human_RBP_ID_8071205,Human_RBP_ID_8178861,Human_RBP_ID_8229690,Human_RBP_ID_9416686,Human_RBP_ID_21967274 RMVar_hsa_circ_161747,RMVar_hsa_circ_82030 96281 RMVar_ID_96281 Human_SNP_ID_521168776 m1A Human chr12 - 131918989 131918971 131918989 AGCCGACACCCCACACACCCTGCACCCCACACACCCGACACCCCACACACCCTGCACCCCACACC AGCCGACACCCCACACACCCTGCACCCCACAC__________________CCTGCACCCCACACC GGTGTGTGGGGTGTCGGGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131918938..131919175 26863196 MeRIP-seq:(Medium) rs1388963045 Functional Loss DEL dbSNP153 33..50 33 - - - 96282 RMVar_ID_96282 Human_SNP_ID_521168793 m1A Human chr12 - 131918989 131918987 131918989 AGCCGACACCCCACACACCCTGCACCCCACACACCCGACACCCCACACACCCTGCACCCCACACC AGCCGACACCCCACACACCCTGCACCCCACAC__CCGACACCCCACACACCCTGCACCCCACACC GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131918938..131919175 26863196 MeRIP-seq:(Medium) rs1413759709 Functional Loss DEL dbSNP153 33..34 33 - - - 96283 RMVar_ID_96283 Human_SNP_ID_521168795 m1A Human chr12 - 131918989 131918989 131918989 AGCCGACACCCCACACACCCTGCACCCCACACACCCGACACCCCACACACCCTGCACCCCACACC AGCCGACACCCCACACACCCTGCACCCCACACCCCCGACACCCCACACACCCTGCACCCCACACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131918938..131919175 26863196 MeRIP-seq:(Medium) rs919890765 Functional Loss SNV dbSNP153 33..33 33 - - - 96284 RMVar_ID_96284 Human_SNP_ID_521169975 m1A Human chr12 + 131921752 131921752 131921752 CTGCTTAGGGAAGGTCAGCAGGCACTGTGCCCAGGAAGAGCCTGCGGCCTCGGCGTCCCCCAGTC CTGCTTAGGGAAGGTCAGCAGGCACTGTGCCCCGGAAGAGCCTGCGGCCTCGGCGTCCCCCAGTC A C ULK1 Ensembl:ENSG00000177169 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131921701..131921825 26863196 MeRIP-seq:(Medium) rs989236215 Functional Loss SNV dbSNP153 33..33 33 - - - 96285 RMVar_ID_96285 Human_SNP_ID_521169976 m1A Human chr12 + 131921752 131921752 131921752 CTGCTTAGGGAAGGTCAGCAGGCACTGTGCCCAGGAAGAGCCTGCGGCCTCGGCGTCCCCCAGTC CTGCTTAGGGAAGGTCAGCAGGCACTGTGCCCGGGAAGAGCCTGCGGCCTCGGCGTCCCCCAGTC A G ULK1 Ensembl:ENSG00000177169 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131921701..131921825 26863196 MeRIP-seq:(Medium) rs989236215 Functional Loss SNV dbSNP153 33..33 33 - - - 96286 RMVar_ID_96286 Human_SNP_ID_521170313 m1A Human chr12 - 131922601 131922601 131922601 TAATCGAGGGCTGGGCAGACCAAGGGAGGCCCAGGCGGGGTTTGCAGGGCATGCCCGCCTGGAAT TAATCGAGGGCTGGGCAGACCAAGGGAGGCCCGGGCGGGGTTTGCAGGGCATGCCCGCCTGGAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131922550..131922679 26863196 MeRIP-seq:(Medium) rs961658555 Functional Loss SNV dbSNP153 33..33 33 - - - 96287 RMVar_ID_96287 Human_SNP_ID_521172851 m1A Human chr12 - 131929382 131929382 131929382 CCAGGTTAACCTCTGACTTCCCCAGCCTCTTCACCTCCCGCCCCGCCCGGTGGGCTTTCCTCAGG CCAGGTTAACCTCTGACTTCCCCAGCCTCTTCCCCTCCCGCCCCGCCCGGTGGGCTTTCCTCAGG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:131929299..131929399 26863410 MeRIP-seq:(Medium) rs956431151 Functional Loss SNV dbSNP153 33..33 33 - - - 96288 RMVar_ID_96288 Human_SNP_ID_521172906 m1A Human chr12 + 131929550 131929549 131929551 AGTGAGGCTGGGGCGTCCAGGTCCGAGAGGTCAGGGGTCAGCTGGAGAGGGGCTGGGGCGCCGGT AGTGAGGCTGGGGCGTCCAGGTCCGAGAGGTC__GGGTCAGCTGGAGAGGGGCTGGGGCGCCGGT CAG C PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131929251..131930209 26863196 MeRIP-seq:(Medium) rs1461797452 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_37069,Human_RBP_ID_260265,Human_RBP_ID_3420135,Human_RBP_ID_4246432,Human_RBP_ID_6153486,Human_RBP_ID_8177659,Human_RBP_ID_9352855,Human_RBP_ID_9416018,Human_RBP_ID_11877969,Human_RBP_ID_17112455,Human_RBP_ID_18934900,Human_RBP_ID_26777622 96289 RMVar_ID_96289 Human_SNP_ID_521172979 m1A Human chr12 - 131929718 131929718 131929718 CCAACAGCGCGCGAAGCTGGAGGCCCATGCGCAGGCTACCAGTGCACCCGACCCCGCCCTGATCC CCAACAGCGCGCGAAGCTGGAGGCCCATGCGCCGGCTACCAGTGCACCCGACCCCGCCCTGATCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:131929364..131929836 26863196 MeRIP-seq:(Medium) rs550249669 Functional Loss SNV dbSNP153 33..33 33 - - - 96290 RMVar_ID_96290 Human_SNP_ID_521173881 m1A Human chr12 - 131932217 131932217 131932217 AATACAGCCTGACCGGACGAGGGCGGACACCAAGTCATCTTCAATTGTTTTGAATTGTGAGGACC AATACAGCCTGACCGGACGAGGGCGGACACCATGTCATCTTCAATTGTTTTGAATTGTGAGGACC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131932176..131932284 26863196 MeRIP-seq:(Medium) rs149011160 Functional Loss SNV dbSNP153 33..33 33 - - - 96291 RMVar_ID_96291 Human_SNP_ID_521173882 m1A Human chr12 - 131932217 131932217 131932217 AATACAGCCTGACCGGACGAGGGCGGACACCAAGTCATCTTCAATTGTTTTGAATTGTGAGGACC AATACAGCCTGACCGGACGAGGGCGGACACCAGGTCATCTTCAATTGTTTTGAATTGTGAGGACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131932176..131932284 26863196 MeRIP-seq:(Medium) rs149011160 Functional Loss SNV dbSNP153 33..33 33 - - - 96292 RMVar_ID_96292 Human_SNP_ID_521173885 m1A Human chr12 - 131932223 131932223 131932223 TTCAGGAATACAGCCTGACCGGACGAGGGCGGACACCAAGTCATCTTCAATTGTTTTGAATTGTG TTCAGGAATACAGCCTGACCGGACGAGGGCGGGCACCAAGTCATCTTCAATTGTTTTGAATTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr12:131932131..131932373;chr12:131932173..131932423 26863196,32194978 MeRIP-seq:(Medium) rs372191433 Functional Loss SNV dbSNP153 33..33 33 - - - 96293 RMVar_ID_96293 Human_SNP_ID_521173916 m1A Human chr12 + 131932290 131932290 131932290 TCATGGTGAGGACATGAGGAAAATGTCCTTCCAGCGCTGCGCCCGGACAGACAAGGTGGGTGGTG TCATGGTGAGGACATGAGGAAAATGTCCTTCCGGCGCTGCGCCCGGACAGACAAGGTGGGTGGTG A G PUS1 Ensembl:ENSG00000177192 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131932144..131932359 26863196 MeRIP-seq:(Medium) rs910629778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875463,Human_RBP_ID_1467966,Human_RBP_ID_1790690,Human_RBP_ID_9365857,Human_RBP_ID_18978267,Human_RBP_ID_19059824,Human_RBP_ID_23547924,Human_RBP_ID_26322398 Human_Splice_Rec_1445561,Human_Splice_Rec_1445571,Human_Splice_Rec_1445575,Human_Splice_Rec_1445585,Human_Splice_Rec_1445597,Human_Splice_Rec_1445607,Human_Splice_Rec_1445613,Human_Splice_Rec_1445617,Human_Splice_Rec_1445623 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_59969,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751,RMVar_hsa_circ_329459 96294 RMVar_ID_96294 Human_SNP_ID_521176691 m1A Human chr12 + 131941622 131941622 131941622 GATCAGGGTGAAGGGCCAGAGCTTCATGATGCATCAGATCCGGAAGATGGTCGGCCTGGTGGTGG GATCAGGGTGAAGGGCCAGAGCTTCATGATGCGTCAGATCCGGAAGATGGTCGGCCTGGTGGTGG A G PUS1 Ensembl:ENSG00000177192 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131941572..131941901 26863196 MeRIP-seq:(Medium) rs753392891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1467998,Human_RBP_ID_1790735,Human_RBP_ID_4212700,Human_RBP_ID_9365859,Human_RBP_ID_11878579,Human_RBP_ID_17813445,Human_RBP_ID_18622050,Human_RBP_ID_22039745,Human_RBP_ID_23547960 RMVar_hsa_circ_110077,RMVar_hsa_circ_161753,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751,RMVar_hsa_circ_97965,RMVar_hsa_circ_340888,RMVar_hsa_circ_161754 96295 RMVar_ID_96295 Human_SNP_ID_521176692 m1A Human chr12 + 131941625 131941625 131941625 CAGGGTGAAGGGCCAGAGCTTCATGATGCATCAGATCCGGAAGATGGTCGGCCTGGTGGTGGCCA CAGGGTGAAGGGCCAGAGCTTCATGATGCATCCGATCCGGAAGATGGTCGGCCTGGTGGTGGCCA A C PUS1 Ensembl:ENSG00000177192 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131941601..131941625 26863196 MeRIP-seq:(Medium) rs863224176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1467998,Human_RBP_ID_1790735,Human_RBP_ID_4212701,Human_RBP_ID_9365859,Human_RBP_ID_11878579,Human_RBP_ID_17813445,Human_RBP_ID_18622050,Human_RBP_ID_22039745,Human_RBP_ID_23547960 RMVar_hsa_circ_110077,RMVar_hsa_circ_161753,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751,RMVar_hsa_circ_97965,RMVar_hsa_circ_340888,RMVar_hsa_circ_161754 96296 RMVar_ID_96296 Human_SNP_ID_521178046 m1A Human chr12 + 131945273 131945273 131945273 GCAGTGAGCTCCTAGGGCGTGGGGTGCCCAAGAGAGTGGAGCTGGTTTTAGGGATTTTGGCCAGA GCAGTGAGCTCCTAGGGCGTGGGGTGCCCAAGGGAGTGGAGCTGGTTTTAGGGATTTTGGCCAGA A G PUS1 Ensembl:ENSG00000177192 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131945263..131945418 26863196 MeRIP-seq:(Medium) rs1192385666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878692 96297 RMVar_ID_96297 Human_SNP_ID_521178055 m1A Human chr12 + 131945303 131945303 131945303 AGAGAGTGGAGCTGGTTTTAGGGATTTTGGCCAGAGGAGCAGTGGGGCTCACTGCTTCGGGAGCC AGAGAGTGGAGCTGGTTTTAGGGATTTTGGCCCGAGGAGCAGTGGGGCTCACTGCTTCGGGAGCC A C PUS1 Ensembl:ENSG00000177192 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131945252..131945364 26863196 MeRIP-seq:(Medium) rs142787061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17813455 96298 RMVar_ID_96298 Human_SNP_ID_521179424 m1A Human chr12 + 131950021 131950021 131950021 ATCCTCCCGCCCTCCTGACGCGGCCGGAGCGCAGCCCTGAGGCCCAGGGTAAGTGAGGGCGGAGG ATCCTCCCGCCCTCCTGACGCGGCCGGAGCGCGGCCCTGAGGCCCAGGGTAAGTGAGGGCGGAGG A G EP400 Ensembl:ENSG00000183495 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131949988..131950129 26863196 MeRIP-seq:(Medium) rs1339288325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874010,Human_RBP_ID_4247156,Human_RBP_ID_5521885,Human_RBP_ID_26322399 Human_Splice_Rec_1445629,Human_Splice_Rec_1445731,Human_Splice_Rec_1445743 96299 RMVar_ID_96299 Human_SNP_ID_521182615 m1A Human chr12 + 131960876 131960876 131960876 CCTGCAGAGCGTGGGCCCTGTCGTCGGGGGAAACCAGCAGATCACACTGGCCCCACTGCCGCTCC CCTGCAGAGCGTGGGCCCTGTCGTCGGGGGAAGCCAGCAGATCACACTGGCCCCACTGCCGCTCC A G EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131960826..131960944 26863196 MeRIP-seq:(Medium) rs117023015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521888,Human_RBP_ID_9367217 RMVar_hsa_circ_16771,RMVar_hsa_circ_367779,RMVar_hsa_circ_266685 96300 RMVar_ID_96300 Human_SNP_ID_521183008 m1A Human chr12 + 131961920 131961918 131961921 GGACATTGAAGAAGAGGAGGAGGAGGAGGAAGAGGAGGAAGAAAAATCTGAGGTTATCAATGACG GGACATTGAAGAAGAGGAGGAGGAGGAGGAA___GAGGAAGAAAAATCTGAGGTTATCAATGACG AGAG A EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131961870..131962002 26863196 MeRIP-seq:(Medium) rs750171862 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_37127,Human_RBP_ID_2313839,Human_RBP_ID_3942493,Human_RBP_ID_8230094,Human_RBP_ID_9365862,Human_RBP_ID_18410950,Human_RBP_ID_22910667,Human_RBP_ID_26322402,Human_RBP_ID_27806275 Human_Splice_Rec_1445631,Human_Splice_Rec_1445733,Human_Splice_Rec_1445745 RMVar_hsa_circ_16771,RMVar_hsa_circ_367779,RMVar_hsa_circ_266685 96301 RMVar_ID_96301 Human_SNP_ID_521183009 m1A Human chr12 + 131961920 131961920 131961920 GGACATTGAAGAAGAGGAGGAGGAGGAGGAAGAGGAGGAAGAAAAATCTGAGGTTATCAATGACG GGACATTGAAGAAGAGGAGGAGGAGGAGGAAGTGGAGGAAGAAAAATCTGAGGTTATCAATGACG A T EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:131961870..131962002 26863196 MeRIP-seq:(Medium) rs1030895151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37127,Human_RBP_ID_2313839,Human_RBP_ID_3942493,Human_RBP_ID_8230094,Human_RBP_ID_9365862,Human_RBP_ID_18410950,Human_RBP_ID_22910667,Human_RBP_ID_26322402,Human_RBP_ID_27806275 Human_Splice_Rec_1445631,Human_Splice_Rec_1445733,Human_Splice_Rec_1445745 RMVar_hsa_circ_16771,RMVar_hsa_circ_367779,RMVar_hsa_circ_266685 96302 RMVar_ID_96302 Human_SNP_ID_521187778 m1A Human chr12 + 131979749 131979749 131979749 GGTAGCAGGGGCCGGAAGCACAGTAGAGACGGACCTGTTTAAGAGGCAGCAGGCGATGCCCTCCA GGTAGCAGGGGCCGGAAGCACAGTAGAGACGGGCCTGTTTAAGAGGCAGCAGGCGATGCCCTCCA A G EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131979655..131979830 26863196 MeRIP-seq:(Medium) rs1280378565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942495,Human_RBP_ID_5554939,Human_RBP_ID_5645111,Human_RBP_ID_9365864,Human_RBP_ID_11878866,Human_RBP_ID_18976491,Human_RBP_ID_26322405 Human_Splice_Rec_1445632,Human_Splice_Rec_1445633,Human_Splice_Rec_1445734,Human_Splice_Rec_1445735,Human_Splice_Rec_1445748,Human_Splice_Rec_1445749 Human_miRNA_ID_2512346,Human_miRNA_ID_3055169 RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_347175,RMVar_hsa_circ_21905,RMVar_hsa_circ_362687,RMVar_hsa_circ_161755,RMVar_hsa_circ_320959 96303 RMVar_ID_96303 Human_SNP_ID_521189711 m1A Human chr12 - 131986582 131986573 131986582 CCGGAGCCACTCACAGGCGCGAGGGACGAGGTAGAAGAGGTGGGCAGAGGCCGTGGGCAGGGCGG CCGGAGCCACTCACAGGCGCGAGGGACGAGGT_________GGGCAGAGGCCGTGGGCAGGGCGG CACCTCTTCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:131986443..131986616 26863196 MeRIP-seq:(Medium) rs767915345 Functional Loss DEL dbSNP153 33..41 33 - - - 96304 RMVar_ID_96304 Human_SNP_ID_521189714 m1A Human chr12 - 131986582 131986582 131986582 CCGGAGCCACTCACAGGCGCGAGGGACGAGGTAGAAGAGGTGGGCAGAGGCCGTGGGCAGGGCGG CCGGAGCCACTCACAGGCGCGAGGGACGAGGTGGAAGAGGTGGGCAGAGGCCGTGGGCAGGGCGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:131986443..131986616 26863196 MeRIP-seq:(Medium) rs1281796482 Functional Loss SNV dbSNP153 33..33 33 - - - 96305 RMVar_ID_96305 Human_SNP_ID_521190106 m1A Human chr12 + 131987889 131987889 131987889 GGAGAGGAGGTGGAAGGTGGCTGCTGCGAAGAAGGTGGGTTGGAATGCGTGGAGCTGCTGTGCTG GGAGAGGAGGTGGAAGGTGGCTGCTGCGAAGATGGTGGGTTGGAATGCGTGGAGCTGCTGTGCTG A T EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131987874..131987939 26863196 MeRIP-seq:(Medium) rs748655549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521890,Human_RBP_ID_18189294,Human_RBP_ID_18410951 Human_Splice_Rec_1445641,Human_Splice_Rec_1445741,Human_Splice_Rec_1445757 RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_347175,RMVar_hsa_circ_27986,RMVar_hsa_circ_27900,RMVar_hsa_circ_362687,RMVar_hsa_circ_161755,RMVar_hsa_circ_318788,RMVar_hsa_circ_113158,RMVar_hsa_circ_322518,RMVar_hsa_circ_161756,RMVar_hsa_circ_352095,RMVar_hsa_circ_115255,RMVar_hsa_circ_161757,RMVar_hsa_circ_161758,RMVar_hsa_circ_161759,RMVar_hsa_circ_123706 96306 RMVar_ID_96306 Human_SNP_ID_521190700 m1A Human chr12 + 131990041 131990041 131990041 GAAGAAAGGGGGAAGAAGGAAGAGCAGAGCAGACTGAGGCGGATAGCCGCCTCCACGGCCCGGGA GAAGAAAGGGGGAAGAAGGAAGAGCAGAGCAGTCTGAGGCGGATAGCCGCCTCCACGGCCCGGGA A T EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:131989940..131990072 26863196 MeRIP-seq:(Medium) rs1403643925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868,Human_RBP_ID_875467,Human_RBP_ID_3942498,Human_RBP_ID_8787469,Human_RBP_ID_18978271,Human_RBP_ID_26322409,Human_RBP_ID_27807473 Human_Splice_Rec_1445642,Human_Splice_Rec_1445742,Human_Splice_Rec_1445758 RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_347175,RMVar_hsa_circ_82298,RMVar_hsa_circ_27986,RMVar_hsa_circ_27900,RMVar_hsa_circ_161755,RMVar_hsa_circ_318788,RMVar_hsa_circ_113158,RMVar_hsa_circ_322518,RMVar_hsa_circ_161756,RMVar_hsa_circ_352095,RMVar_hsa_circ_161758,RMVar_hsa_circ_161759,RMVar_hsa_circ_123706,RMVar_hsa_circ_361958,RMVar_hsa_circ_161760 96307 RMVar_ID_96307 Human_SNP_ID_521201643 m1A Human chr12 - 132029915 132029915 132029915 CCGGTGCAGCTCCCGCACGGGCCACGCCCCCAACTGCCGCATACCTGAGTCGAACTGCACCAGCC CCGGTGCAGCTCCCGCACGGGCCACGCCCCCAGCTGCCGCATACCTGAGTCGAACTGCACCAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132029905..132030006 32194978 MeRIP-seq:(Medium) rs376749084 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 96308 RMVar_ID_96308 Human_SNP_ID_521208616 m1A Human chr12 + 132053497 132053497 132053497 CAGCCAGCCGCCAGCAGGGCCACCAGCTGTCCAGCCCCAACCCCAGCCACAGCCCCAGACCCAGC CAGCCAGCCGCCAGCAGGGCCACCAGCTGTCCGGCCCCAACCCCAGCCACAGCCCCAGACCCAGC A G EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132053450..132053538 26863196 MeRIP-seq:(Medium) rs1223636759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27806292 Human_miRNA_ID_1161857 RMVar_hsa_circ_48648,RMVar_hsa_circ_6549,RMVar_hsa_circ_269086,RMVar_hsa_circ_298045,RMVar_hsa_circ_43921,RMVar_hsa_circ_161771,RMVar_hsa_circ_18459,RMVar_hsa_circ_40263 96309 RMVar_ID_96309 Human_SNP_ID_521212108 m1A Human chr12 + 132064727 132064727 132064727 AAACTGCAGATGCCCCCGCAGCCCCCACCGCCACAGGCCCAGTCTGCGCCCCCGCAGCCAACAGC AAACTGCAGATGCCCCCGCAGCCCCCACCGCCCCAGGCCCAGTCTGCGCCCCCGCAGCCAACAGC A C EP400 Ensembl:ENSG00000183495 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132064676..132064850 26863196 MeRIP-seq:(Medium) rs751516430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1445720,Human_Splice_Rec_1445792 RMVar_hsa_circ_48648,RMVar_hsa_circ_269086,RMVar_hsa_circ_43921,RMVar_hsa_circ_18459,RMVar_hsa_circ_29240,RMVar_hsa_circ_52828,RMVar_hsa_circ_75010 96310 RMVar_ID_96310 Human_SNP_ID_521213412 m1A Human chr12 + 132069224 132069224 132069224 GGTGTCAGGGTGCCCCACCAGCCCGACTATTCAGGGAGCAGTGTCCCGGGTGGGGTGGGCTGCAG GGTGTCAGGGTGCCCCACCAGCCCGACTATTCTGGGAGCAGTGTCCCGGGTGGGGTGGGCTGCAG A T EP400 Ensembl:ENSG00000183495 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132069148..132069498 26863196 MeRIP-seq:(Medium) rs1315384605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6153992,Human_RBP_ID_21967284 RMVar_hsa_circ_269086,RMVar_hsa_circ_18459,RMVar_hsa_circ_29240,RMVar_hsa_circ_52828,RMVar_hsa_circ_75010,RMVar_hsa_circ_269813 96311 RMVar_ID_96311 Human_SNP_ID_521217636 m1A Human chr12 - 132084504 132084504 132084504 TGGGACGGAGAGAGGGGAGCGCGCGGCCGGGGAGCCTCGAGGGTAACCGGCGGATGTGGGCGGTC TGGGACGGAGAGAGGGGAGCGCGCGGCCGGGGTGCCTCGAGGGTAACCGGCGGATGTGGGCGGTC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:132084356..132084580 26863196 MeRIP-seq:(Medium) rs1009137522 Functional Loss SNV dbSNP153 33..33 33 - - - 96312 RMVar_ID_96312 Human_SNP_ID_521234413 m1A Human chr12 - 132143186 132143186 132143186 GGTCAAGGTTGGGGGTTGGGGGTGCCAGGCAGAGGCCTCGAGGCAGGGACGCCGGCGTGGCTGGG GGTCAAGGTTGGGGGTTGGGGGTGCCAGGCAGCGGCCTCGAGGCAGGGACGCCGGCGTGGCTGGG T G DDX51 Ensembl:ENSG00000185163 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132143003..132143325 26863196 MeRIP-seq:(Medium) rs1335193606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755150,Human_RBP_ID_5347963,Human_RBP_ID_8177665,Human_RBP_ID_19060791,Human_RBP_ID_22645680,Human_RBP_ID_23256022,Human_RBP_ID_26777635 96313 RMVar_ID_96313 Human_SNP_ID_521234789 m1A Human chr12 - 132143903 132143903 132143903 CTGCCGGGTGGGTGTCTGCCTCGCAGAAAGCAACGAGGAGGCGCCAGGGGAGCCCAGCGCAGGGA CTGCCGGGTGGGTGTCTGCCTCGCAGAAAGCAGCGAGGAGGCGCCAGGGGAGCCCAGCGCAGGGA T C DDX51 Ensembl:ENSG00000185163 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr12:132143779..132144188;chr12:132143809..132144077 26863196 MeRIP-seq:(Medium) rs1375021766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1445944 96314 RMVar_ID_96314 Human_SNP_ID_521234891 m1A Human chr12 - 132144104 132144104 132144104 CCGAGGCGGCTGCATCGACCGAGCCGGCGACCAGGAGGCGACGGCGGCCCCGGCGGCGGCGGCGG CCGAGGCGGCTGCATCGACCGAGCCGGCGACCGGGAGGCGACGGCGGCCCCGGCGGCGGCGGCGG T C DDX51 Ensembl:ENSG00000185163 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132143251..132144236 32194978 MeRIP-seq:(Medium) rs1357396829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229616,Human_RBP_ID_875498,Human_RBP_ID_4213159 96315 RMVar_ID_96315 Human_SNP_ID_521238649 m1A Human chr12 - 132151547 132151547 132151547 AAAGGCAGGACCATGAGCAGGGCCTCAGGGGGAGCCGTCAGGGCCAGGCGGGCCAGCCGCTTGGC AAAGGCAGGACCATGAGCAGGGCCTCAGGGGGCGCCGTCAGGGCCAGGCGGGCCAGCCGCTTGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132151299..132152325 26863196 MeRIP-seq:(Medium) rs761112309 Functional Loss SNV dbSNP153 33..33 33 - - - 96316 RMVar_ID_96316 Human_SNP_ID_521239135 m1A Human chr12 + 132152382 132152382 132152382 CCTGCTGGGACGGCCGGGTGAACTCTGTGCCCAGCACTTCACGCTCAGCTGACCCTGGCCCACCT CCTGCTGGGACGGCCGGGTGAACTCTGTGCCCGGCACTTCACGCTCAGCTGACCCTGGCCCACCT A G NOC4L Ensembl:ENSG00000184967 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132152254..132152381 26863196 MeRIP-seq:(Medium) rs1300506798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8370036,Human_RBP_ID_21884904 Human_miRNA_ID_2316155,Human_miRNA_ID_2319310,Human_miRNA_ID_2322469,Human_miRNA_ID_2325638,Human_miRNA_ID_2328754,Human_miRNA_ID_2520015,Human_miRNA_ID_2523180,Human_miRNA_ID_2775028,Human_miRNA_ID_2822377,Human_miRNA_ID_2828505,Human_miRNA_ID_2831662,Human_miRNA_ID_2835781,Human_miRNA_ID_2841137 RMVar_hsa_circ_161785,RMVar_hsa_circ_83251 96317 RMVar_ID_96317 Human_SNP_ID_521287590 m1A Human chr12 + 132286076 132286076 132286076 GCCAGCACGGGGGAGCGCTCACTTTCCCGGCCAGCGTGGGGGGCGGTCACTTCCCCGGCGGGCGT GCCAGCACGGGGGAGCGCTCACTTTCCCGGCCGGCGTGGGGGGCGGTCACTTCCCCGGCGGGCGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132286072..132286181 26863196 MeRIP-seq:(Medium) rs953795176 Functional Loss SNV dbSNP153 33..33 33 - - - 96318 RMVar_ID_96318 Human_SNP_ID_521357736 m1A Human chr12 - 132490232 132490232 132490232 GGGCCGAGCGGGCGGGGCCGGGCGGGCGCGGCAGGCGGCAGGCGGGAGGCGGCCGGGCTCCTGGG GGGCCGAGCGGGCGGGGCCGGGCGGGCGCGGCTGGCGGCAGGCGGGAGGCGGCCGGGCTCCTGGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:132490191..132490276;chr12:132490186..132490298 26863196 MeRIP-seq:(Medium) rs910371699 Functional Loss SNV dbSNP153 33..33 33 - - - 96319 RMVar_ID_96319 Human_SNP_ID_521357737 m1A Human chr12 - 132490232 132490232 132490232 GGGCCGAGCGGGCGGGGCCGGGCGGGCGCGGCAGGCGGCAGGCGGGAGGCGGCCGGGCTCCTGGG GGGCCGAGCGGGCGGGGCCGGGCGGGCGCGGCGGGCGGCAGGCGGGAGGCGGCCGGGCTCCTGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:132490191..132490276;chr12:132490186..132490298 26863196 MeRIP-seq:(Medium) rs910371699 Functional Loss SNV dbSNP153 33..33 33 - - - 96320 RMVar_ID_96320 Human_SNP_ID_521357752 m1A Human chr12 - 132490258 132490258 132490258 CGCCCCATGCGCGCGGCGCGGCGATCGGGCCGAGCGGGCGGGGCCGGGCGGGCGCGGCAGGCGGC CGCCCCATGCGCGCGGCGCGGCGATCGGGCCGGGCGGGCGGGGCCGGGCGGGCGCGGCAGGCGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:132490176..132490845 26863410 MeRIP-seq:(Medium) rs1382302112 Functional Loss SNV dbSNP153 33..33 33 - - - 96321 RMVar_ID_96321 Human_SNP_ID_521357978 m1A Human chr12 + 132490809 132490809 132490809 CCGCCGCCGCGAGTCCAGCTCGCAGGAGGAGGAGGTCATCGACGGCTTCGCCATCGCCAGCTTCA CCGCCGCCGCGAGTCCAGCTCGCAGGAGGAGGTGGTCATCGACGGCTTCGCCATCGCCAGCTTCA A T FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132490446..132507063 32194978 MeRIP-seq:(Medium) rs1485833707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942547,Human_RBP_ID_9322899 Human_Splice_Rec_1446189,Human_Splice_Rec_1446221 96322 RMVar_ID_96322 Human_SNP_ID_521360748 m1A Human chr12 + 132499536 132499536 132499536 GGATGGCAGTAAAGAGTCTGTCGTCGAAGGCTAGGAGTCACAGAGGAGGCCACGAGGGCTTCTGG GGATGGCAGTAAAGAGTCTGTCGTCGAAGGCTGGGAGTCACAGAGGAGGCCACGAGGGCTTCTGG A G FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132499533..132499682 26863196 MeRIP-seq:(Medium) rs1472139523 Functional Loss SNV dbSNP153 33..33 33 - - - 96323 RMVar_ID_96323 Human_SNP_ID_521363896 m1A Human chr12 + 132509362 132509362 132509362 GCGGCCACTCCTGGGTCAGCGCAGCTGGCCCCAGCGGTCACTTCTGGGCCTGAAACAGCCCTGCC GCGGCCACTCCTGGGTCAGCGCAGCTGGCCCCCGCGGTCACTTCTGGGCCTGAAACAGCCCTGCC A C FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132509355..132509555 32194978 MeRIP-seq:(Medium) rs1173972504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415328 RMVar_hsa_circ_18378,RMVar_hsa_circ_116276,RMVar_hsa_circ_361524,RMVar_hsa_circ_161790 96324 RMVar_ID_96324 Human_SNP_ID_521364033 m1A Human chr12 - 132509647 132509647 132509647 TGCAGCGGTGCCTTGGGGCCAGGAGGAACCGCAGGCGCCGGCAGTAGAGGCAGGGGACCAGGAGG TGCAGCGGTGCCTTGGGGCCAGGAGGAACCGCGGGCGCCGGCAGTAGAGGCAGGGGACCAGGAGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:132509551..132509904 26863410 MeRIP-seq:(Medium) rs956545031 Functional Loss SNV dbSNP153 33..33 33 - - - 96325 RMVar_ID_96325 Human_SNP_ID_521364222 m1A Human chr12 + 132510160 132510160 132510160 GCGGCCGCTCATGGGCCCAGAGCAGCCCTGCCAGCCCCTGCGGCCGCTCATGGGCCCCAACAAGC GCGGCCGCTCATGGGCCCAGAGCAGCCCTGCCCGCCCCTGCGGCCGCTCATGGGCCCCAACAAGC A C FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132510151..132510352 26863196 MeRIP-seq:(Medium) rs1399340354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18378,RMVar_hsa_circ_116276,RMVar_hsa_circ_361524,RMVar_hsa_circ_161790 96326 RMVar_ID_96326 Human_SNP_ID_521364398 m1A Human chr12 + 132510650 132510650 132510650 GCTCGGCCAGAGGCGGGAGCCCCTACAGTGCCACGATCAGGCTGAGGCTCACCACACCAGGAAGA GCTCGGCCAGAGGCGGGAGCCCCTACAGTGCCGCGATCAGGCTGAGGCTCACCACACCAGGAAGA A G FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132510301..132511347 32194978 MeRIP-seq:(Medium) rs1416618355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3419390,Human_RBP_ID_5139995,Human_RBP_ID_8070641,Human_RBP_ID_11881497,Human_RBP_ID_17813637,Human_RBP_ID_22710413,Human_RBP_ID_23548447,Human_RBP_ID_24366262 RMVar_hsa_circ_18378,RMVar_hsa_circ_116276,RMVar_hsa_circ_361524,RMVar_hsa_circ_161790 96327 RMVar_ID_96327 Human_SNP_ID_521366575 m1A Human chr12 - 132517592 132517592 132517592 GTCTAACGGTGCCTTCTCTCCTTCCCAGGCACAGCTGTGCTCACACTCAGAACAGTCTCCACCCG GTCTAACGGTGCCTTCTCTCCTTCCCAGGCACGGCTGTGCTCACACTCAGAACAGTCTCCACCCG T C HSALNG0095313 RNACentral:URS0000EA5264 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132517585..132517720 26863196 MeRIP-seq:(Medium) rs1223118740 Functional Loss SNV dbSNP153 33..33 33 - - - 96328 RMVar_ID_96328 Human_SNP_ID_521367393 m1A Human chr12 - 132520200 132520200 132520200 AGGGTGCAAGGAGGGTGTGCTGGAGGGGTGCAAGGAGGGTGTGCTGGAGGGGTACAAGGAGGGTT AGGGTGCAAGGAGGGTGTGCTGGAGGGGTGCACGGAGGGTGTGCTGGAGGGGTACAAGGAGGGTT T G HSALNG0095313 RNACentral:URS0000EA5264 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:132520094..132520224 26863196 MeRIP-seq:(Medium) rs1248948865 Functional Loss SNV dbSNP153 33..33 33 - - - 96329 RMVar_ID_96329 Human_SNP_ID_521369583 m1A Human chr12 - 132527679 132527651 132527679 CCCCACAGCCCCGCAGCCCACAACCCTGCCCCACAGCCCCGCAGCCCACAACCCTGCCCCGCAGC CCCCACAGCCCCGCAGCCCACAACCCTGCCCC____________________________GCAGC CGGGGCAGGGTTGTGGGCTGCGGGGCTGT C HSALNG0095313 RNACentral:URS0000EA5264 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132527667..132527826 26863196 MeRIP-seq:(Medium) rs753823919 Functional Loss DEL dbSNP153 33..60 33 - - - 96330 RMVar_ID_96330 Human_SNP_ID_521369599 m1A Human chr12 - 132527679 132527679 132527679 CCCCACAGCCCCGCAGCCCACAACCCTGCCCCACAGCCCCGCAGCCCACAACCCTGCCCCGCAGC CCCCACAGCCCCGCAGCCCACAACCCTGCCCCGCAGCCCCGCAGCCCACAACCCTGCCCCGCAGC T C HSALNG0095313 RNACentral:URS0000EA5264 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132527667..132527826 26863196 MeRIP-seq:(Medium) rs1202674920 Functional Loss SNV dbSNP153 33..33 33 - - - 96331 RMVar_ID_96331 Human_SNP_ID_521369600 m1A Human chr12 - 132527679 132527679 132527679 CCCCACAGCCCCGCAGCCCACAACCCTGCCCCACAGCCCCGCAGCCCACAACCCTGCCCCGCAGC CCCCACAGCCCCGCAGCCCACAACCCTGCCCCCCAGCCCCGCAGCCCACAACCCTGCCCCGCAGC T G HSALNG0095313 RNACentral:URS0000EA5264 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132527667..132527826 26863196 MeRIP-seq:(Medium) rs1202674920 Functional Loss SNV dbSNP153 33..33 33 - - - 96332 RMVar_ID_96332 Human_SNP_ID_521372809 m1A Human chr12 - 132537000 132537000 132537000 TCCACTCTACCCCACCCCACGTCAGCCTGAAGACCCCCGAGTGCCTGCAGAGCCCCTGGCCTCAC TCCACTCTACCCCACCCCACGTCAGCCTGAAGGCCCCCGAGTGCCTGCAGAGCCCCTGGCCTCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132536993..132537085 26863196 MeRIP-seq:(Medium) rs1270476659 Functional Loss SNV dbSNP153 33..33 33 - - - 96333 RMVar_ID_96333 Human_SNP_ID_521375113 m1A Human chr12 + 132544664 132544664 132544664 TTGAGGATGGTGACGTGAGGACGGCGATACTGATGATCATGGTGGTGGTAATGAGGATGGTGTTG TTGAGGATGGTGACGTGAGGACGGCGATACTGGTGATCATGGTGGTGGTAATGAGGATGGTGTTG A G FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132544575..132544835 26863196 MeRIP-seq:(Medium) rs1250841406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23548653,Human_RBP_ID_27571975 RMVar_hsa_circ_116276,RMVar_hsa_circ_161790,RMVar_hsa_circ_319916 96334 RMVar_ID_96334 Human_SNP_ID_521376891 m1A Human chr12 + 132550254 132550254 132550254 GGAGGACGGCAGGGGAGCGGAGAGGGGCTGCCAGCCTTTCTCCAGGGCAGAACTTCGGGTCACGC GGAGGACGGCAGGGGAGCGGAGAGGGGCTGCCGGCCTTTCTCCAGGGCAGAACTTCGGGTCACGC A G FBRSL1 Ensembl:ENSG00000112787 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132550144..132550418 26863196 MeRIP-seq:(Medium) rs1025582292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260319,Human_RBP_ID_872803,Human_RBP_ID_3418821,Human_RBP_ID_5172892,Human_RBP_ID_5235633,Human_RBP_ID_5314792,Human_RBP_ID_5347969,Human_RBP_ID_8070729,Human_RBP_ID_8177759,Human_RBP_ID_8229809,Human_RBP_ID_8725462,Human_RBP_ID_9416712,Human_RBP_ID_18410795,Human_RBP_ID_21967298,Human_RBP_ID_22414836,Human_RBP_ID_22472415,Human_RBP_ID_22522476,Human_RBP_ID_22645690,Human_RBP_ID_22710015,Human_RBP_ID_26322452,Human_RBP_ID_26422920,Human_RBP_ID_26768316,Human_RBP_ID_26776980,Human_RBP_ID_27572030 RMVar_hsa_circ_116276,RMVar_hsa_circ_161790 96335 RMVar_ID_96335 Human_SNP_ID_521383823 m1A Human chr12 + 132570118 132570108 132570118 TCCCTTGGTGAAGAAGGAACCCCCCGCCCCGCACCGCCACACCCCGCAGCCGCCACCCCCGCAGC TCCCTTGGTGAAGAAGGAACCCC__________CCGCCACACCCCGCAGCCGCCACCCCCGCAGC CCCGCCCCGCA C FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:132570019..132570375 26863196 MeRIP-seq:(Medium) rs1566224712 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_415346 Human_miRNA_ID_3065994 RMVar_hsa_circ_116276,RMVar_hsa_circ_80489,RMVar_hsa_circ_161790,RMVar_hsa_circ_161791 96336 RMVar_ID_96336 Human_SNP_ID_521383855 m1A Human chr12 + 132570148 132570148 132570148 GCACCGCCACACCCCGCAGCCGCCACCCCCGCAGCCCCGCGGCCTGCTCCCGACACACGTGCCTG GCACCGCCACACCCCGCAGCCGCCACCCCCGCGGCCCCGCGGCCTGCTCCCGACACACGTGCCTG A G FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132560037..132570525 26863196 MeRIP-seq:(Medium) rs1042327909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1446201,Human_Splice_Rec_1446233 Human_miRNA_ID_3065995 RMVar_hsa_circ_116276,RMVar_hsa_circ_80489,RMVar_hsa_circ_161790,RMVar_hsa_circ_161791 96337 RMVar_ID_96337 Human_SNP_ID_521383900 m1A Human chr12 - 132570229 132570229 132570229 GTCCCCCGCGGGGACCCCACCTGAGGCCGTGCAGGCCGTTGGCTGCCGCCTGGCTGTGGCCCGCG GTCCCCCGCGGGGACCCCACCTGAGGCCGTGCGGGCCGTTGGCTGCCGCCTGGCTGTGGCCCGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132570178..132570372 32194978 MeRIP-seq:(Medium) rs1403644013 Functional Loss SNV dbSNP153 33..33 33 - - - 96338 RMVar_ID_96338 Human_SNP_ID_521388685 m1A Human chr12 + 132583152 132583152 132583152 AGAGCCGCTCCCCGGCCAAGGAGGAGGCCGCCAAGATGCCCGCGCGCGCATCCCCGCCCCACAGC AGAGCCGCTCCCCGGCCAAGGAGGAGGCCGCCGAGATGCCCGCGCGCGCATCCCCGCCCCACAGC A G FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132583036..132583668 26863196 MeRIP-seq:(Medium) rs1237724028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17813666 Human_miRNA_ID_2250171 RMVar_hsa_circ_80836,RMVar_hsa_circ_91181,RMVar_hsa_circ_161792,RMVar_hsa_circ_161793 96339 RMVar_ID_96339 Human_SNP_ID_521388687 m1A Human chr12 + 132583155 132583155 132583155 GCCGCTCCCCGGCCAAGGAGGAGGCCGCCAAGATGCCCGCGCGCGCATCCCCGCCCCACAGCAAG GCCGCTCCCCGGCCAAGGAGGAGGCCGCCAAGGTGCCCGCGCGCGCATCCCCGCCCCACAGCAAG A G FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132582136..132583950 26863196 MeRIP-seq:(Medium) rs1448567550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17813666 Human_miRNA_ID_2250171,Human_miRNA_ID_2988281 RMVar_hsa_circ_80836,RMVar_hsa_circ_91181,RMVar_hsa_circ_161792,RMVar_hsa_circ_161793 96340 RMVar_ID_96340 Human_SNP_ID_521389013 m1A Human chr12 + 132583668 132583660 132583669 CGCCCCCCCTGGTGACGGCGGCCGGGCCCCCCACGCCCCCCGGGCCGCCGCGGAGCCGGACTACT CGCCCCCCCTGGTGACGGCGGCCGG_________GCCCCCCGGGCCGCCGCGGAGCCGGACTACT GGCCCCCCAC G FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:132583527..132583709 26863196 MeRIP-seq:(Medium) rs1225144569 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_22532541 RMVar_hsa_circ_80836,RMVar_hsa_circ_91181,RMVar_hsa_circ_161792,RMVar_hsa_circ_161793 96341 RMVar_ID_96341 Human_SNP_ID_521389023 m1A Human chr12 + 132583668 132583668 132583668 CGCCCCCCCTGGTGACGGCGGCCGGGCCCCCCACGCCCCCCGGGCCGCCGCGGAGCCGGACTACT CGCCCCCCCTGGTGACGGCGGCCGGGCCCCCCGCGCCCCCCGGGCCGCCGCGGAGCCGGACTACT A G FBRSL1 Ensembl:ENSG00000112787 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:132583527..132583709 26863196 MeRIP-seq:(Medium) rs894765917 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22532541 RMVar_hsa_circ_80836,RMVar_hsa_circ_91181,RMVar_hsa_circ_161792,RMVar_hsa_circ_161793 96342 RMVar_ID_96342 Human_SNP_ID_521403533 m1A Human chr12 + 132625722 132625721 132625723 CACCAGCGTCATCTCGATGGCAGAGGAGTCGTAGGGCGCCTGACAGTTGGAGCAGAGCCACTGAG CACCAGCGTCATCTCGATGGCAGAGGAGTCGT__GGCGCCTGACAGTTGGAGCAGAGCCACTGAG TAG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132625248..132626262 32194978 MeRIP-seq:(Medium) rs1271136597 Functional Loss DEL dbSNP153 33..34 33 - - - 96343 RMVar_ID_96343 Human_SNP_ID_521405559 m1A Human chr12 - 132632693 132632693 132632693 GAGGAGGAGGGGGGCCAGCCAGCTCTCCCAGGAGGCCGAGGGGGCGGTCGGAGCCCTTCCCGGTG GAGGAGGAGGGGGGCCAGCCAGCTCTCCCAGGTGGCCGAGGGGGCGGTCGGAGCCCTTCCCGGTG T A POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132632657..132632808 32194978 MeRIP-seq:(Medium) rs751818136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521910,Human_RBP_ID_18410976,Human_RBP_ID_22910842,Human_RBP_ID_27806297 Human_Splice_Rec_1446559,Human_Splice_Rec_1446581,Human_Splice_Rec_1446639,Human_Splice_Rec_1446735,Human_Splice_Rec_1446829,Human_Splice_Rec_1446925,Human_Splice_Rec_1446935,Human_Splice_Rec_1446955,Human_Splice_Rec_1446963,Human_Splice_Rec_1446973 Clinvar_Rec_549,Clinvar_Rec_550 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_328891,RMVar_hsa_circ_161813,RMVar_hsa_circ_29399,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96344 RMVar_ID_96344 Human_SNP_ID_521405560 m1A Human chr12 - 132632693 132632693 132632693 GAGGAGGAGGGGGGCCAGCCAGCTCTCCCAGGAGGCCGAGGGGGCGGTCGGAGCCCTTCCCGGTG GAGGAGGAGGGGGGCCAGCCAGCTCTCCCAGGGGGCCGAGGGGGCGGTCGGAGCCCTTCCCGGTG T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132632657..132632808 32194978 MeRIP-seq:(Medium) rs751818136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5521910,Human_RBP_ID_18410976,Human_RBP_ID_22910842,Human_RBP_ID_27806297 Human_Splice_Rec_1446559,Human_Splice_Rec_1446581,Human_Splice_Rec_1446639,Human_Splice_Rec_1446735,Human_Splice_Rec_1446829,Human_Splice_Rec_1446925,Human_Splice_Rec_1446935,Human_Splice_Rec_1446955,Human_Splice_Rec_1446963,Human_Splice_Rec_1446973 Clinvar_Rec_549,Clinvar_Rec_550 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_328891,RMVar_hsa_circ_161813,RMVar_hsa_circ_29399,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96345 RMVar_ID_96345 Human_SNP_ID_521406045 m1A Human chr12 - 132634254 132634254 132634254 GGAATCCAACGTGGAGGATTTACTGGAAAACAACTGGAACATTTTGCAGTTTTTGCCACAGGCAG GGAATCCAACGTGGAGGATTTACTGGAAAACAGCTGGAACATTTTGCAGTTTTTGCCACAGGCAG T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132634203..132634304 32194978 MeRIP-seq:(Medium) rs775893052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942569,Human_RBP_ID_9443975,Human_RBP_ID_18257572,Human_RBP_ID_22901316,Human_RBP_ID_26322477 Human_Splice_Rec_1446557,Human_Splice_Rec_1446579,Human_Splice_Rec_1446637,Human_Splice_Rec_1446733,Human_Splice_Rec_1446827,Human_Splice_Rec_1446923,Human_Splice_Rec_1446953,Human_Splice_Rec_1446961,Human_Splice_Rec_1446971,Human_Splice_Rec_1446977 Clinvar_Rec_551,Clinvar_Rec_552 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_29399,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96346 RMVar_ID_96346 Human_SNP_ID_521406046 m1A Human chr12 - 132634254 132634254 132634254 GGAATCCAACGTGGAGGATTTACTGGAAAACAACTGGAACATTTTGCAGTTTTTGCCACAGGCAG GGAATCCAACGTGGAGGATTTACTGGAAAACACCTGGAACATTTTGCAGTTTTTGCCACAGGCAG T G POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132634203..132634304 32194978 MeRIP-seq:(Medium) rs775893052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3942569,Human_RBP_ID_9443975,Human_RBP_ID_18257572,Human_RBP_ID_22901316,Human_RBP_ID_26322477 Human_Splice_Rec_1446557,Human_Splice_Rec_1446579,Human_Splice_Rec_1446637,Human_Splice_Rec_1446733,Human_Splice_Rec_1446827,Human_Splice_Rec_1446923,Human_Splice_Rec_1446953,Human_Splice_Rec_1446961,Human_Splice_Rec_1446971,Human_Splice_Rec_1446977 Clinvar_Rec_551,Clinvar_Rec_552 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_29399,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96347 RMVar_ID_96347 Human_SNP_ID_521406072 m1A Human chr12 - 132634287 132634287 132634287 GGAAAGAGATGGGGAGGAGGAGGAAGAGGCGGAGGAATCCAACGTGGAGGATTTACTGGAAAACA GGAAAGAGATGGGGAGGAGGAGGAAGAGGCGGCGGAATCCAACGTGGAGGATTTACTGGAAAACA T G POLE Ensembl:ENSG00000177084 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:132634237..132634424;chr12:132634237..132634415 26863196 MeRIP-seq:(Medium) rs894413549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3943988,Human_RBP_ID_4213663,Human_RBP_ID_5521912,Human_RBP_ID_8247591,Human_RBP_ID_9443975,Human_RBP_ID_18622402,Human_RBP_ID_18978328,Human_RBP_ID_22901316,Human_RBP_ID_24950352,Human_RBP_ID_26322477 Human_Splice_Rec_1446556,Human_Splice_Rec_1446578,Human_Splice_Rec_1446636,Human_Splice_Rec_1446732,Human_Splice_Rec_1446826,Human_Splice_Rec_1446922,Human_Splice_Rec_1446952,Human_Splice_Rec_1446960,Human_Splice_Rec_1446970,Human_Splice_Rec_1446976,Human_Splice_Rec_1446980 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_29399,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96348 RMVar_ID_96348 Human_SNP_ID_521406116 m1A Human chr12 + 132634372 132634372 132634372 CTGCTCATCCTCTGCTCCCCCTGCTTTCTGGGAGTCTTGCTGTAACACATGAGACAACGCGGCTG CTGCTCATCCTCTGCTCCCCCTGCTTTCTGGGCGTCTTGCTGTAACACATGAGACAACGCGGCTG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:132634276..132634417 26863196 MeRIP-seq:(Medium) rs760770350 Functional Loss SNV dbSNP153 33..33 33 - - - 96349 RMVar_ID_96349 Human_SNP_ID_521406117 m1A Human chr12 + 132634372 132634372 132634372 CTGCTCATCCTCTGCTCCCCCTGCTTTCTGGGAGTCTTGCTGTAACACATGAGACAACGCGGCTG CTGCTCATCCTCTGCTCCCCCTGCTTTCTGGGGGTCTTGCTGTAACACATGAGACAACGCGGCTG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:132634276..132634417 26863196 MeRIP-seq:(Medium) rs760770350 Functional Loss SNV dbSNP153 33..33 33 - - - 96350 RMVar_ID_96350 Human_SNP_ID_521406297 m1A Human chr12 - 132634981 132634981 132634981 GACGCAGACGCTTCTGGGAGCTGGCAGGATGAAGCCAAGACTGCCCAGGACACCTGGATGGGAGC GACGCAGACGCTTCTGGGAGCTGGCAGGATGATGCCAAGACTGCCCAGGACACCTGGATGGGAGC T A POLE Ensembl:ENSG00000177084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132634979..132635516 26863196 MeRIP-seq:(Medium) rs1310827309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11882150 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96351 RMVar_ID_96351 Human_SNP_ID_521406314 m1A Human chr12 - 132635049 132635049 132635049 TGGACTGAGAGGAAGCTGTGGGTACCAGAGCCAGGGGCTCAGATGTCAGAGGGAAAGCCCTTTGT TGGACTGAGAGGAAGCTGTGGGTACCAGAGCCGGGGGCTCAGATGTCAGAGGGAAAGCCCTTTGT T C POLE Ensembl:ENSG00000177084 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132635044..132635408 26863196 MeRIP-seq:(Medium) rs576023203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11882151,Human_RBP_ID_21968059 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_92425,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161803,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_83960,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_161814,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815 96352 RMVar_ID_96352 Human_SNP_ID_521407654 m1A Human chr12 + 132639435 132639433 132639435 GTCCAAATCCGTCACTGTCGCCTCCCCTTCTCACTGTCCCCACCTTAAGTCACGGTCCAAATTTC GTCCAAATCCGTCACTGTCGCCTCCCCTTCT__CTGTCCCCACCTTAAGTCACGGTCCAAATTTC TCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132639385..132639502 26863196 MeRIP-seq:(Medium) rs1264127113 Functional Loss DEL dbSNP153 32..33 33 - - - 96353 RMVar_ID_96353 Human_SNP_ID_521408589 m1A Human chr12 - 132642524 132642524 132642524 TCACTACCTCAACCTGGACACCTGCCTGTCGCAGGCCTTCGAGATGAGCAGGTGAGCACAGTACT TCACTACCTCAACCTGGACACCTGCCTGTCGCGGGCCTTCGAGATGAGCAGGTGAGCACAGTACT T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:132642501..132642525 32194978 MeRIP-seq:(Medium) rs878854879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9365895,Human_RBP_ID_18978339 Human_Splice_Rec_1446545,Human_Splice_Rec_1446625,Human_Splice_Rec_1446721,Human_Splice_Rec_1446815,Human_Splice_Rec_1446911 Human_miRNA_ID_836623 Clinvar_Rec_553 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_118030,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_102801,RMVar_hsa_circ_161801,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161802,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_72574,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_38612,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815,RMVar_hsa_circ_106863,RMVar_hsa_circ_105628,RMVar_hsa_circ_120801,RMVar_hsa_circ_161816,RMVar_hsa_circ_111490,RMVar_hsa_circ_161817,RMVar_hsa_circ_161819,RMVar_hsa_circ_77366,RMVar_hsa_circ_96215,RMVar_hsa_circ_161820,RMVar_hsa_circ_161821,RMVar_hsa_circ_113950,RMVar_hsa_circ_161818,RMVar_hsa_circ_85516,RMVar_hsa_circ_161822,RMVar_hsa_circ_19838,RMVar_hsa_circ_161823 96354 RMVar_ID_96354 Human_SNP_ID_521418547 m1A Human chr12 - 132673606 132673606 132673606 AGGCTATGATCCCGTGGAGCTAGACCCGGAGGACATGTGCCGGATGGCCACGGAGCAGCCCCAGG AGGCTATGATCCCGTGGAGCTAGACCCGGAGGGCATGTGCCGGATGGCCACGGAGCAGCCCCAGG T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132673261..132675498 32194978 MeRIP-seq:(Medium) rs1555228601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_260043,Human_RBP_ID_415418,Human_RBP_ID_872841,Human_RBP_ID_3942597,Human_RBP_ID_5521928,Human_RBP_ID_8787089,Human_RBP_ID_9280010,Human_RBP_ID_9365922,Human_RBP_ID_11882820,Human_RBP_ID_18417689,Human_RBP_ID_18469287,Human_RBP_ID_18622523,Human_RBP_ID_18976557,Human_RBP_ID_22910673,Human_RBP_ID_26321050 Clinvar_Rec_554,Clinvar_Rec_8781 RMVar_hsa_circ_126340,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_111490,RMVar_hsa_circ_161821,RMVar_hsa_circ_3208,RMVar_hsa_circ_95609,RMVar_hsa_circ_161826,RMVar_hsa_circ_86964,RMVar_hsa_circ_161825,RMVar_hsa_circ_24861,RMVar_hsa_circ_161833,RMVar_hsa_circ_126856,RMVar_hsa_circ_119070,RMVar_hsa_circ_117860,RMVar_hsa_circ_161836,RMVar_hsa_circ_161837,RMVar_hsa_circ_40064,RMVar_hsa_circ_106941,RMVar_hsa_circ_84577,RMVar_hsa_circ_161844,RMVar_hsa_circ_161845 96355 RMVar_ID_96355 Human_SNP_ID_521418961 m1A Human chr12 - 132674913 132674913 132674913 AGACAGGTGGATGTGGAAATGCCAACAGAAGGAGGCTGGAAGGGAAGGAAGGGAAGGGAGGGAGG AGACAGGTGGATGTGGAAATGCCAACAGAAGGTGGCTGGAAGGGAAGGAAGGGAAGGGAGGGAGG T A POLE Ensembl:ENSG00000177084 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132674909..132675081 26863196 MeRIP-seq:(Medium) rs1030391540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126340,RMVar_hsa_circ_89914,RMVar_hsa_circ_161795,RMVar_hsa_circ_161794,RMVar_hsa_circ_111490,RMVar_hsa_circ_161821,RMVar_hsa_circ_3208,RMVar_hsa_circ_95609,RMVar_hsa_circ_161826,RMVar_hsa_circ_86964,RMVar_hsa_circ_161825,RMVar_hsa_circ_24861,RMVar_hsa_circ_119070,RMVar_hsa_circ_117860,RMVar_hsa_circ_161836,RMVar_hsa_circ_161837,RMVar_hsa_circ_40064,RMVar_hsa_circ_106941,RMVar_hsa_circ_84577,RMVar_hsa_circ_161844,RMVar_hsa_circ_161845 96356 RMVar_ID_96356 Human_SNP_ID_521420992 m1A Human chr12 - 132681226 132681226 132681226 AGTTTCGGCACTCAAGCGCCTGGAACGGAGTCAGTGGACGGATAAGATGGATTTGCGGTTTGGTT AGTTTCGGCACTCAAGCGCCTGGAACGGAGTCGGTGGACGGATAAGATGGATTTGCGGTTTGGTT T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132681176..132681304 26863196 MeRIP-seq:(Medium) rs1467498021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1468349,Human_RBP_ID_4252921,Human_RBP_ID_11883035,Human_RBP_ID_22911108,Human_RBP_ID_23548855 Human_Splice_Rec_1446476,Human_Splice_Rec_1446477,Human_Splice_Rec_1446650,Human_Splice_Rec_1446651,Human_Splice_Rec_1446746,Human_Splice_Rec_1446747,Human_Splice_Rec_1446844,Human_Splice_Rec_1446845,Human_Splice_Rec_1447007,Human_Splice_Rec_1447010 RMVar_hsa_circ_126340,RMVar_hsa_circ_161794,RMVar_hsa_circ_3208,RMVar_hsa_circ_86964,RMVar_hsa_circ_161825,RMVar_hsa_circ_24861,RMVar_hsa_circ_117860,RMVar_hsa_circ_161837,RMVar_hsa_circ_53289,RMVar_hsa_circ_161849,RMVar_hsa_circ_316547,RMVar_hsa_circ_161851,RMVar_hsa_circ_331611,RMVar_hsa_circ_161852,RMVar_hsa_circ_161853,RMVar_hsa_circ_274567 96357 RMVar_ID_96357 Human_SNP_ID_521422627 m1A Human chr12 - 132687169 132687169 132687169 GGGCCGTCCTCGGCTGGCGCCGCCGAGGCGGGAGGGAGGCCCGGTTCCCGCAGCCGCCCGCACTC GGGCCGTCCTCGGCTGGCGCCGCCGAGGCGGGGGGGAGGCCCGGTTCCCGCAGCCGCCCGCACTC T C POLE Ensembl:ENSG00000177084 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:132687160..132687301 26863196 MeRIP-seq:(Medium) rs919971183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5350557,Human_RBP_ID_8177773,Human_RBP_ID_19060825 RMVar_hsa_circ_126340,RMVar_hsa_circ_161794,RMVar_hsa_circ_161853 96358 RMVar_ID_96358 Human_SNP_ID_521422727 m1A Human chr12 - 132687306 132687306 132687306 CAGAGGTGGTAGCCAACGGCTCCATGTCTCTGAGGAGCGGCGGGCGGCGGCGCGCGGACCCAGGC CAGAGGTGGTAGCCAACGGCTCCATGTCTCTGGGGAGCGGCGGGCGGCGGCGCGCGGACCCAGGC T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:132687147..132687350 26863196 MeRIP-seq:(Medium) rs1010746038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229329,Human_RBP_ID_4247165,Human_RBP_ID_18417373,Human_RBP_ID_22910850,Human_RBP_ID_26322533 Human_Splice_Rec_1446475,Human_Splice_Rec_1446649,Human_Splice_Rec_1446745,Human_Splice_Rec_1446843,Human_Splice_Rec_1447009 Clinvar_Rec_555 RMVar_hsa_circ_126340,RMVar_hsa_circ_161794,RMVar_hsa_circ_161853 96359 RMVar_ID_96359 Human_SNP_ID_521422733 m1A Human chr12 + 132687314 132687314 132687314 CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACATGGAGCCGTTGGCTACCACCTCTGCTTCAGGG CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACCTGGAGCCGTTGGCTACCACCTCTGCTTCAGGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:132687190..132687326 26863196 MeRIP-seq:(Medium) rs879254126 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_556,Clinvar_Rec_557,Clinvar_Rec_558 96360 RMVar_ID_96360 Human_SNP_ID_521422734 m1A Human chr12 + 132687314 132687314 132687314 CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACATGGAGCCGTTGGCTACCACCTCTGCTTCAGGG CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACGTGGAGCCGTTGGCTACCACCTCTGCTTCAGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:132687190..132687326 26863196 MeRIP-seq:(Medium) rs879254126 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_556,Clinvar_Rec_557,Clinvar_Rec_558 96361 RMVar_ID_96361 Human_SNP_ID_521422735 m1A Human chr12 + 132687314 132687314 132687314 CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACATGGAGCCGTTGGCTACCACCTCTGCTTCAGGG CCGCGCGCCGCCGCCCGCCGCTCCTCAGAGACTTGGAGCCGTTGGCTACCACCTCTGCTTCAGGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:132687190..132687326 26863196 MeRIP-seq:(Medium) rs879254126 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_556,Clinvar_Rec_557,Clinvar_Rec_558 96362 RMVar_ID_96362 Human_SNP_ID_521422746 m1A Human chr12 - 132687323 132687323 132687323 AAATTTCTCCCCTGAAGCAGAGGTGGTAGCCAACGGCTCCATGTCTCTGAGGAGCGGCGGGCGGC AAATTTCTCCCCTGAAGCAGAGGTGGTAGCCAGCGGCTCCATGTCTCTGAGGAGCGGCGGGCGGC T C POLE Ensembl:ENSG00000177084 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132687180..132687350 26863196 MeRIP-seq:(Medium) rs1057521786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247165,Human_RBP_ID_18417373,Human_RBP_ID_22910850,Human_RBP_ID_26322533 Human_Splice_Rec_1446475,Human_Splice_Rec_1446649,Human_Splice_Rec_1446745,Human_Splice_Rec_1446843,Human_Splice_Rec_1447009 RMVar_hsa_circ_126340,RMVar_hsa_circ_161794,RMVar_hsa_circ_161853 96363 RMVar_ID_96363 Human_SNP_ID_521422747 m1A Human chr12 - 132687323 132687323 132687323 AAATTTCTCCCCTGAAGCAGAGGTGGTAGCCAACGGCTCCATGTCTCTGAGGAGCGGCGGGCGGC AAATTTCTCCCCTGAAGCAGAGGTGGTAGCCACCGGCTCCATGTCTCTGAGGAGCGGCGGGCGGC T G POLE Ensembl:ENSG00000177084 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132687180..132687350 26863196 MeRIP-seq:(Medium) rs1057521786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247165,Human_RBP_ID_18417373,Human_RBP_ID_22910850,Human_RBP_ID_26322533 Human_Splice_Rec_1446475,Human_Splice_Rec_1446649,Human_Splice_Rec_1446745,Human_Splice_Rec_1446843,Human_Splice_Rec_1447009 RMVar_hsa_circ_126340,RMVar_hsa_circ_161794,RMVar_hsa_circ_161853 96364 RMVar_ID_96364 Human_SNP_ID_521422908 m1A Human chr12 + 132687666 132687666 132687666 GGGTCGGTGCCCCCGGCGGCACGGCGCTGGGGAGGCGATGGCGCCGGCCGCGTCCAGGCTGCGGG GGGTCGGTGCCCCCGGCGGCACGGCGCTGGGGCGGCGATGGCGCCGGCCGCGTCCAGGCTGCGGG A C PXMP2 Ensembl:ENSG00000176894 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132687543..132687839 26863196 MeRIP-seq:(Medium) rs548077770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415422,Human_RBP_ID_4246441,Human_RBP_ID_8940759,Human_RBP_ID_18417578,Human_RBP_ID_18433919 96365 RMVar_ID_96365 Human_SNP_ID_521422911 m1A Human chr12 + 132687671 132687671 132687671 GGTGCCCCCGGCGGCACGGCGCTGGGGAGGCGATGGCGCCGGCCGCGTCCAGGCTGCGGGCCGAA GGTGCCCCCGGCGGCACGGCGCTGGGGAGGCGGTGGCGCCGGCCGCGTCCAGGCTGCGGGCCGAA A G PXMP2 Ensembl:ENSG00000176894 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:132687508..132690270;chr12:132687492..132687800;chr12:132687494..132687752 26863196 MeRIP-seq:(Medium) rs898291250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415422,Human_RBP_ID_4246441,Human_RBP_ID_8940759,Human_RBP_ID_18417578,Human_RBP_ID_18433919,Human_RBP_ID_22492867 96366 RMVar_ID_96366 Human_SNP_ID_521422912 m1A Human chr12 + 132687671 132687671 132687671 GGTGCCCCCGGCGGCACGGCGCTGGGGAGGCGATGGCGCCGGCCGCGTCCAGGCTGCGGGCCGAA GGTGCCCCCGGCGGCACGGCGCTGGGGAGGCGTTGGCGCCGGCCGCGTCCAGGCTGCGGGCCGAA A T PXMP2 Ensembl:ENSG00000176894 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:132687508..132690270;chr12:132687492..132687800;chr12:132687494..132687752 26863196 MeRIP-seq:(Medium) rs898291250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415422,Human_RBP_ID_4246441,Human_RBP_ID_8940759,Human_RBP_ID_18417578,Human_RBP_ID_18433919,Human_RBP_ID_22492867 96367 RMVar_ID_96367 Human_SNP_ID_521422921 m1A Human chr12 - 132687693 132687682 132687693 GCGGCAGCGCCCCGAGCCCGGCTTCGGCCCGCAGCCTGGACGCGGCCGGCGCCATCGCCTCCCCA GCGGCAGCGCCCCGAGCCCGGCTTCGGCCCGC___________GGCCGGCGCCATCGCCTCCCCA CGCGTCCAGGCT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:132687671..132687754 26863410 MeRIP-seq:(Medium) rs1310265965 Functional Loss DEL dbSNP153 33..43 33 - - - 96368 RMVar_ID_96368 Human_SNP_ID_521422946 m1A Human chr12 - 132687735 132687735 132687735 GGTAGAGCCGCAGGAAGAGCAGGTACTGGGCGAGCGCCCGCCGCGGCAGCGCCCCGAGCCCGGCT GGTAGAGCCGCAGGAAGAGCAGGTACTGGGCGGGCGCCCGCCGCGGCAGCGCCCCGAGCCCGGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:132687601..132690270 26863410 MeRIP-seq:(Medium) rs1317362449 Functional Loss SNV dbSNP153 33..33 33 - - - 96369 RMVar_ID_96369 Human_SNP_ID_521422962 m1A Human chr12 + 132687744 132687744 132687744 CGGGGCGCTGCCGCGGCGGGCGCTCGCCCAGTACCTGCTCTTCCTGCGGCTCTACCCGGTGCTCA CGGGGCGCTGCCGCGGCGGGCGCTCGCCCAGTTCCTGCTCTTCCTGCGGCTCTACCCGGTGCTCA A T PXMP2 Ensembl:ENSG00000176894 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:132687654..132687752 26863410 MeRIP-seq:(Medium) rs762632319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415423,Human_RBP_ID_4213904,Human_RBP_ID_8940759,Human_RBP_ID_17469716 Human_Splice_Rec_1447011,Human_Splice_Rec_1447019 96370 RMVar_ID_96370 Human_SNP_ID_521422965 m1A Human chr12 - 132687747 132687747 132687747 TGGTGAGCACCGGGTAGAGCCGCAGGAAGAGCAGGTACTGGGCGAGCGCCCGCCGCGGCAGCGCC TGGTGAGCACCGGGTAGAGCCGCAGGAAGAGCGGGTACTGGGCGAGCGCCCGCCGCGGCAGCGCC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:132687646..132687748 26863410 MeRIP-seq:(Medium) rs1370293539 Functional Loss SNV dbSNP153 33..33 33 - - - 96371 RMVar_ID_96371 Human_SNP_ID_521422982 m1A Human chr12 + 132687779 132687779 132687779 TGCTCTTCCTGCGGCTCTACCCGGTGCTCACCAAGGCGGCCACCAGGTGAGCGGGGGCGCGGGAA TGCTCTTCCTGCGGCTCTACCCGGTGCTCACCCAGGCGGCCACCAGGTGAGCGGGGGCGCGGGAA A C PXMP2 Ensembl:ENSG00000176894 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132687601..132687800 26863196 MeRIP-seq:(Medium) rs1379824486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_875560,Human_RBP_ID_4247167,Human_RBP_ID_18433920 Human_Splice_Rec_1447011,Human_Splice_Rec_1447019 96372 RMVar_ID_96372 Human_SNP_ID_521423069 m1A Human chr12 - 132688040 132688040 132688040 CTGTTGGGTCCTTGGGTGGAACCTCAGCGCCGACCCCCGGGTCTGGGCGGGCCCTCCACGCGCTG CTGTTGGGTCCTTGGGTGGAACCTCAGCGCCGGCCCCCGGGTCTGGGCGGGCCCTCCACGCGCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132688033..132688314 26863196 MeRIP-seq:(Medium) rs1308782813 Functional Loss SNV dbSNP153 33..33 33 - - - 96373 RMVar_ID_96373 Human_SNP_ID_521423161 m1A Human chr12 - 132688206 132688195 132688207 CCCCCAAGACCCGCTCCCCTCGCCCTGTCTTCACCCGCGCCCCGCAGACCCGCTCCCCTCGCCCT CCCCCAAGACCCGCTCCCCTCGCCCTGTCTT____________GCAGACCCGCTCCCCTCGCCCT CGGGGCGCGGGTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132688191..132688336 26863196 MeRIP-seq:(Medium) rs1565988121 Functional Loss DEL dbSNP153 32..43 33 - - - 96374 RMVar_ID_96374 Human_SNP_ID_521423165 m1A Human chr12 - 132688206 132688206 132688206 CCCCCAAGACCCGCTCCCCTCGCCCTGTCTTCACCCGCGCCCCGCAGACCCGCTCCCCTCGCCCT CCCCCAAGACCCGCTCCCCTCGCCCTGTCTTCCCCCGCGCCCCGCAGACCCGCTCCCCTCGCCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132688191..132688336 26863196 MeRIP-seq:(Medium) rs1258710251 Functional Loss SNV dbSNP153 33..33 33 - - - 96375 RMVar_ID_96375 Human_SNP_ID_521423433 m1A Human chr12 - 132689211 132689211 132689211 CCCGCTCCCCTGGCCCTGTCTTCACCCGCACCACGCAGACCCGCTCCCTTGGCCCTGTCTTTACC CCCGCTCCCCTGGCCCTGTCTTCACCCGCACCCCGCAGACCCGCTCCCTTGGCCCTGTCTTTACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132689197..132689512 26863196 MeRIP-seq:(Medium) rs1379203903 Functional Loss SNV dbSNP153 33..33 33 - - - 96376 RMVar_ID_96376 Human_SNP_ID_521423445 m1A Human chr12 + 132689227 132689227 132689227 AGGGAGCGGGTCTGCGTGGTGCGGGTGAAGACAGGGCCAGGGGAGCGGGTCCACATGGAGCGTGT AGGGAGCGGGTCTGCGTGGTGCGGGTGAAGACGGGGCCAGGGGAGCGGGTCCACATGGAGCGTGT A G PXMP2,AC135586.2 Ensembl:ENSG00000176894,Ensembl:ENSG00000256632 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132689220..132689540 26863196 MeRIP-seq:(Medium) rs1471789101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96377 RMVar_ID_96377 Human_SNP_ID_521430297 m1A Human chr12 - 132710878 132710878 132710878 AGGCCGCCAGCTGCAGCGCCTGCCGGAACGCCATGCCGCTTGCTCCCGCGCCGGCCCGCGCAGGC AGGCCGCCAGCTGCAGCGCCTGCCGGAACGCCTTGCCGCTTGCTCCCGCGCCGGCCCGCGCAGGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132710830..132710990 26863196 MeRIP-seq:(Medium) rs1168889820 Functional Loss SNV dbSNP153 33..33 33 - - - 96378 RMVar_ID_96378 Human_SNP_ID_521430298 m1A Human chr12 - 132710878 132710878 132710878 AGGCCGCCAGCTGCAGCGCCTGCCGGAACGCCATGCCGCTTGCTCCCGCGCCGGCCCGCGCAGGC AGGCCGCCAGCTGCAGCGCCTGCCGGAACGCCGTGCCGCTTGCTCCCGCGCCGGCCCGCGCAGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132710830..132710990 26863196 MeRIP-seq:(Medium) rs1168889820 Functional Loss SNV dbSNP153 33..33 33 - - - 96379 RMVar_ID_96379 Human_SNP_ID_521430308 m1A Human chr12 + 132710899 132710899 132710899 AGCAAGCGGCATGGCGTTCCGGCAGGCGCTGCAGCTGGCGGCCTGCGGGCTGGCCGGGGGCTCGG AGCAAGCGGCATGGCGTTCCGGCAGGCGCTGCCGCTGGCGGCCTGCGGGCTGGCCGGGGGCTCGG A C PGAM5,AC135586.2 Ensembl:ENSG00000247077,Ensembl:ENSG00000256632 Protein coding,lincRNA CDS,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:132710803..132711109 26863196 MeRIP-seq:(Medium) rs1251110339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229529,Human_RBP_ID_4246442,Human_RBP_ID_8940760,Human_RBP_ID_9365940,Human_RBP_ID_17669031,Human_RBP_ID_17813730,Human_RBP_ID_24551334,Human_RBP_ID_26422926,Human_RBP_ID_27836888 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96380 RMVar_ID_96380 Human_SNP_ID_521430336 m1A Human chr12 + 132710989 132710989 132710989 GGTAGGGAAGCCGCGCGCAGGCGGGGACGCGGAGCCACGCCCGGCTGAGCCGCCGGCCTGGGCGG GGTAGGGAAGCCGCGCGCAGGCGGGGACGCGGGGCCACGCCCGGCTGAGCCGCCGGCCTGGGCGG A G PGAM5,AC135586.2 Ensembl:ENSG00000247077,Ensembl:ENSG00000256632 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:132710801..132711129;chr12:132710801..132711121;chr12:132710776..132711113 26863196 MeRIP-seq:(Medium) rs1006643745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754566,Human_RBP_ID_876781,Human_RBP_ID_4213955,Human_RBP_ID_8940760,Human_RBP_ID_9365940,Human_RBP_ID_17650931,Human_RBP_ID_26421931 Human_Splice_Rec_1447045,Human_Splice_Rec_1447055 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96381 RMVar_ID_96381 Human_SNP_ID_521431425 m1A Human chr12 - 132714795 132714793 132714795 GACCTCTGTTCCCAAGTTTGAGTTTTTCTGACAAGATGTTATTTCCAAATTGTCAGACTATTTGG GACCTCTGTTCCCAAGTTTGAGTTTTTCTGAC__GATGTTATTTCCAAATTGTCAGACTATTTGG CTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:132714793..132714925 26863410 MeRIP-seq:(Medium) rs1015164772 Functional Loss DEL dbSNP153 33..34 33 - - - 96382 RMVar_ID_96382 Human_SNP_ID_521431426 m1A Human chr12 - 132714795 132714795 132714795 GACCTCTGTTCCCAAGTTTGAGTTTTTCTGACAAGATGTTATTTCCAAATTGTCAGACTATTTGG GACCTCTGTTCCCAAGTTTGAGTTTTTCTGACGAGATGTTATTTCCAAATTGTCAGACTATTTGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:132714793..132714925 26863410 MeRIP-seq:(Medium) rs1475924465 Functional Loss SNV dbSNP153 33..33 33 - - - 96383 RMVar_ID_96383 Human_SNP_ID_521431443 m1A Human chr12 - 132714854 132714851 132714854 GCACGTTGATCAGAGACAGTGGTTCTCGCCTGATGTTGAAATACAAGATATGTCCTTGAGACCTC GCACGTTGATCAGAGACAGTGGTTCTCGCCTG___TTGAAATACAAGATATGTCCTTGAGACCTC ACAT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:132714851..132714875 26863196 MeRIP-seq:(Medium) rs997698176 Functional Loss DEL dbSNP153 33..35 33 - - - 96384 RMVar_ID_96384 Human_SNP_ID_521431472 m1A Human chr12 - 132714906 132714906 132714906 TGGTCCAGCTTGGACGCCAGCTCTTCTTCCCCAGATTCCACGTTCCTCTTCCGCACGTTGATCAG TGGTCCAGCTTGGACGCCAGCTCTTCTTCCCCGGATTCCACGTTCCTCTTCCGCACGTTGATCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:132714813..132715090;chr12:132714819..132714975;chr12:132714797..132714975 26863196 MeRIP-seq:(Medium) rs759587288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8370340 96385 RMVar_ID_96385 Human_SNP_ID_521432579 m1A Human chr12 + 132717727 132717727 132717727 TGTGCTTCTCTGCAGGCGTCTGCAAAGTCAGCACAGATCTGCTGCGGGAAGGCGCCCCCATCGAG TGTGCTTCTCTGCAGGCGTCTGCAAAGTCAGCGCAGATCTGCTGCGGGAAGGCGCCCCCATCGAG A G PGAM5 Ensembl:ENSG00000247077 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132717532..132718014 32194978 MeRIP-seq:(Medium) rs1269831423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4213969,Human_RBP_ID_18189032,Human_RBP_ID_26904394,Human_RBP_ID_27212777 Human_Splice_Rec_1447050,Human_Splice_Rec_1447051,Human_Splice_Rec_1447060,Human_Splice_Rec_1447061,Human_Splice_Rec_1447070,Human_Splice_Rec_1447071,Human_Splice_Rec_1447078,Human_Splice_Rec_1447079 Human_miRNA_ID_2949331 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598,RMVar_hsa_circ_271750,RMVar_hsa_circ_161859 96386 RMVar_ID_96386 Human_SNP_ID_521432781 m1A Human chr12 - 132718122 132718122 132718122 ATTTTAGACCACGCCCAGCCCAGCAGCTGCCTACCTGCACACGATGTAGCGGATGACGTTGGCGT ATTTTAGACCACGCCCAGCCCAGCAGCTGCCTGCCTGCACACGATGTAGCGGATGACGTTGGCGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132718112..132718951 32194978 MeRIP-seq:(Medium) rs1478022000 Functional Loss SNV dbSNP153 33..33 33 - - - 96387 RMVar_ID_96387 Human_SNP_ID_521434006 m1A Human chr12 + 132721174 132721174 132721174 TGAGGGTCCAGGCTCCATTGGCAAAGCCGGTCAGGCACGAGGGCGACTGAGGCACGTGGATGAGG TGAGGGTCCAGGCTCCATTGGCAAAGCCGGTCGGGCACGAGGGCGACTGAGGCACGTGGATGAGG A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:132721126..132721200 32194978 MeRIP-seq:(Medium) rs927356143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6154894,Human_RBP_ID_11883389,Human_RBP_ID_17237233,Human_RBP_ID_17353121,Human_RBP_ID_22793687,Human_RBP_ID_24464867,Human_RBP_ID_26414305,Human_RBP_ID_26806362,Human_RBP_ID_27212790 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598,RMVar_hsa_circ_161860 96388 RMVar_ID_96388 Human_SNP_ID_521434060 m1A Human chr12 + 132721380 132721380 132721380 AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGACAAGGCAACAT AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCCGGAGTTCAAGACCAGCCTGGACAAGGCAACAT A C PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78601523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178374,Human_RBP_ID_22492875,Human_RBP_ID_22573976,Human_RBP_ID_23157069,Human_RBP_ID_23305752,Human_RBP_ID_26414311,Human_RBP_ID_27420550 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96389 RMVar_ID_96389 Human_SNP_ID_521434061 m1A Human chr12 + 132721380 132721380 132721380 AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGACAAGGCAACAT AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCGGGAGTTCAAGACCAGCCTGGACAAGGCAACAT A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78601523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178374,Human_RBP_ID_22492875,Human_RBP_ID_22573976,Human_RBP_ID_23157069,Human_RBP_ID_23305752,Human_RBP_ID_26414311,Human_RBP_ID_27420550 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96390 RMVar_ID_96390 Human_SNP_ID_521434191 m1A Human chr12 + 132721837 132721837 132721837 ATTGTTCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATTCACCCACCTTGGCCTCCCAAAGTGC ATTGTTCAGGCTGGTCTCGAACTCCCAACCTCGGGTGATTCACCCACCTTGGCCTCCCAAAGTGC A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11548879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6154917,Human_RBP_ID_26414323,Human_RBP_ID_27420554 Human_miRNA_ID_2697489 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96391 RMVar_ID_96391 Human_SNP_ID_521434192 m1A Human chr12 + 132721842 132721842 132721842 TCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATTCACCCACCTTGGCCTCCCAAAGTGCTGGGA TCAGGCTGGTCTCGAACTCCCAACCTCAGGTGGTTCACCCACCTTGGCCTCCCAAAGTGCTGGGA A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs556691096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26414323,Human_RBP_ID_27420554 Human_miRNA_ID_2697489 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 96392 RMVar_ID_96392 Human_SNP_ID_521440240 m1A Human chr12 - 132738137 132738137 132738137 TGTGATAAACTACAAGAGAAGCAGGATTGAGAAGCAGGATTGAGAAGCGAGGAGGCCGGGCACAG TGTGATAAACTACAAGAGAAGCAGGATTGAGACGCAGGATTGAGAAGCGAGGAGGCCGGGCACAG T G ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132738038..132738202 26863196 MeRIP-seq:(Medium) rs1434021547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35591,Human_RBP_ID_229312,Human_RBP_ID_22172505 RMVar_hsa_circ_16334,RMVar_hsa_circ_115866,RMVar_hsa_circ_79270,RMVar_hsa_circ_161861,RMVar_hsa_circ_239,RMVar_hsa_circ_161862,RMVar_hsa_circ_74067,RMVar_hsa_circ_343748,RMVar_hsa_circ_269762,RMVar_hsa_circ_48223,RMVar_hsa_circ_346841,RMVar_hsa_circ_42149,RMVar_hsa_circ_325536,RMVar_hsa_circ_378674,RMVar_hsa_circ_161866 96393 RMVar_ID_96393 Human_SNP_ID_521441650 m1A Human chr12 + 132742732 132742732 132742732 CACCATCGTCACCATCATCACCACCACTGCCAACACCACCATGATCATTGCTATCTCCATCCTCA CACCATCGTCACCATCATCACCACCACTGCCACCACCACCATGATCATTGCTATCTCCATCCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132742686..132742806 26863196 MeRIP-seq:(Medium) rs377532430 Functional Loss SNV dbSNP153 33..33 33 - - - 96394 RMVar_ID_96394 Human_SNP_ID_521441651 m1A Human chr12 + 132742732 132742732 132742732 CACCATCGTCACCATCATCACCACCACTGCCAACACCACCATGATCATTGCTATCTCCATCCTCA CACCATCGTCACCATCATCACCACCACTGCCATCACCACCATGATCATTGCTATCTCCATCCTCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132742686..132742806 26863196 MeRIP-seq:(Medium) rs377532430 Functional Loss SNV dbSNP153 33..33 33 - - - 96395 RMVar_ID_96395 Human_SNP_ID_521443477 m1A Human chr12 - 132748263 132748263 132748263 AAGAGCGAGCGAACAGTTACAAAAATCCCCGCACGCAGGACCTCACCGCCAAGCTTCGGAAAGCT AAGAGCGAGCGAACAGTTACAAAAATCCCCGCTCGCAGGACCTCACCGCCAAGCTTCGGAAAGCT T A ANKLE2 Ensembl:ENSG00000176915 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132748109..132748288 26863196 MeRIP-seq:(Medium) rs770106915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229315,Human_RBP_ID_4214220,Human_RBP_ID_6155054,Human_RBP_ID_8779129,Human_RBP_ID_17813801 Human_Splice_Rec_1447088,Human_Splice_Rec_1447110,Human_Splice_Rec_1447184,Human_Splice_Rec_1447194 Human_miRNA_ID_2007259 RMVar_hsa_circ_16334,RMVar_hsa_circ_115866,RMVar_hsa_circ_161861,RMVar_hsa_circ_74067,RMVar_hsa_circ_343748,RMVar_hsa_circ_269762,RMVar_hsa_circ_346841,RMVar_hsa_circ_70709,RMVar_hsa_circ_42149,RMVar_hsa_circ_325536,RMVar_hsa_circ_340723,RMVar_hsa_circ_161866,RMVar_hsa_circ_334301,RMVar_hsa_circ_161867,RMVar_hsa_circ_335813,RMVar_hsa_circ_161871,RMVar_hsa_circ_271957,RMVar_hsa_circ_161869,RMVar_hsa_circ_295351,RMVar_hsa_circ_304540,RMVar_hsa_circ_161873,RMVar_hsa_circ_161872 96396 RMVar_ID_96396 Human_SNP_ID_521448059 m1A Human chr12 + 132761286 132761271 132761287 GGTTTCCTCCCCGCGCCGCCCTCCTTTGGGCCATCCCTCCCCAGGTCTCGAGAGACCGCAGCAAG GGTTTCCTCCCCGCGCCG________________CCCTCCCCAGGTCTCGAGAGACCGCAGCAAG GCCCTCCTTTGGGCCAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132761283..132761371 26863196 MeRIP-seq:(Medium) rs1312381472 Functional Loss DEL dbSNP153 19..34 33 - - - 96397 RMVar_ID_96397 Human_SNP_ID_521452161 m1A Human chr12 - 132773157 132773157 132773157 GCCCCCGGGGGGTCACGCCGGCCCACGCGGCGACCCACAGAGACACAGTCAGAGCAGGGCTTCCA GCCCCCGGGGGGTCACGCCGGCCCACGCGGCGTCCCACAGAGACACAGTCAGAGCAGGGCTTCCA T A GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132773107..132773258 32194978 MeRIP-seq:(Medium) rs747258920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82224,RMVar_hsa_circ_76294,RMVar_hsa_circ_111370,RMVar_hsa_circ_161875,RMVar_hsa_circ_101820,RMVar_hsa_circ_161876,RMVar_hsa_circ_161877,RMVar_hsa_circ_161878 96398 RMVar_ID_96398 Human_SNP_ID_521452663 m1A Human chr12 + 132774293 132774293 132774293 CGGGATCTTGATGGGCGTGGCAGGGTTGGAAGAGCTGGCCTCGCCTTTCGGCTCCTTTCTCTGTT CGGGATCTTGATGGGCGTGGCAGGGTTGGAAGGGCTGGCCTCGCCTTTCGGCTCCTTTCTCTGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132774129..132774351 26863196 MeRIP-seq:(Medium) rs576675283 Functional Loss SNV dbSNP153 33..33 33 - - - 96399 RMVar_ID_96399 Human_SNP_ID_521452965 m1A Human chr12 - 132775209 132775209 132775209 TGCTCCAGGCAAAAGTGTCGGAGCTGAAGAACAACATGAAGACCCTGCTCCAGCAGAACCAGCAG TGCTCCAGGCAAAAGTGTCGGAGCTGAAGAACCACATGAAGACCCTGCTCCAGCAGAACCAGCAG T G GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132775111..132775218 26863196 MeRIP-seq:(Medium) rs779002581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_990950,Human_RBP_ID_1791188,Human_RBP_ID_5111857,Human_RBP_ID_9255632,Human_RBP_ID_9280017,Human_RBP_ID_9365958,Human_RBP_ID_11884356 Human_Splice_Rec_1447240,Human_Splice_Rec_1447241,Human_Splice_Rec_1447286,Human_Splice_Rec_1447287,Human_Splice_Rec_1447292,Human_Splice_Rec_1447338 RMVar_hsa_circ_82224,RMVar_hsa_circ_76294,RMVar_hsa_circ_111370,RMVar_hsa_circ_161875,RMVar_hsa_circ_19413,RMVar_hsa_circ_161877,RMVar_hsa_circ_161878,RMVar_hsa_circ_63608,RMVar_hsa_circ_268857,RMVar_hsa_circ_340011 96400 RMVar_ID_96400 Human_SNP_ID_521455655 m1A Human chr12 - 132782378 132782378 132782378 GAAAGGGAAGCTTACGGGCCTCGGTCAGTCCAACGCAGCTCTGCGGGAACACAACAGCATCCTAG GAAAGGGAAGCTTACGGGCCTCGGTCAGTCCAGCGCAGCTCTGCGGGAACACAACAGCATCCTAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132782268..132782433 26863196 MeRIP-seq:(Medium) rs765767645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_876354,Human_RBP_ID_3398895,Human_RBP_ID_9365963,Human_RBP_ID_18622722 Human_Splice_Rec_1447231,Human_Splice_Rec_1447277,Human_Splice_Rec_1447329 Human_miRNA_ID_1980898,Human_miRNA_ID_1982622 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_368835,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_294782,RMVar_hsa_circ_316454,RMVar_hsa_circ_60268,RMVar_hsa_circ_75106,RMVar_hsa_circ_161882,RMVar_hsa_circ_161883,RMVar_hsa_circ_161884,RMVar_hsa_circ_302166,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_161885 96401 RMVar_ID_96401 Human_SNP_ID_521456286 m1A Human chr12 - 132784214 132784214 132784214 AAAAGGAACTGCAGGAGGTCATAGCGCTGACCAGCCAGGAGCTGGAGGAGTCCCGGGAGAAGGTG AAAAGGAACTGCAGGAGGTCATAGCGCTGACCGGCCAGGAGCTGGAGGAGTCCCGGGAGAAGGTG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132784084..132784247 26863196 MeRIP-seq:(Medium) rs1380136518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8787098,Human_RBP_ID_9365964,Human_RBP_ID_18622726,Human_RBP_ID_18978414,Human_RBP_ID_22039776,Human_RBP_ID_22910682,Human_RBP_ID_23118075,Human_RBP_ID_24543232,Human_RBP_ID_26322556,Human_RBP_ID_27807538 Human_Splice_Rec_1447228,Human_Splice_Rec_1447229,Human_Splice_Rec_1447274,Human_Splice_Rec_1447275,Human_Splice_Rec_1447326,Human_Splice_Rec_1447327,Human_Splice_Rec_1447368 Human_miRNA_ID_2332287,Human_miRNA_ID_2965373 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_294782,RMVar_hsa_circ_60268,RMVar_hsa_circ_75106,RMVar_hsa_circ_161883,RMVar_hsa_circ_161884,RMVar_hsa_circ_302166,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_161885 96402 RMVar_ID_96402 Human_SNP_ID_521456297 m1A Human chr12 - 132784234 132784234 132784234 TCATAGCAAGACGCTGCTGGAAAAGGAACTGCAGGAGGTCATAGCGCTGACCAGCCAGGAGCTGG TCATAGCAAGACGCTGCTGGAAAAGGAACTGCCGGAGGTCATAGCGCTGACCAGCCAGGAGCTGG T G GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132784185..132784260 26863196 MeRIP-seq:(Medium) rs1221774558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33715,Human_RBP_ID_1791198,Human_RBP_ID_9365964,Human_RBP_ID_11884471,Human_RBP_ID_18433934,Human_RBP_ID_18622726,Human_RBP_ID_18978414,Human_RBP_ID_22910682,Human_RBP_ID_24543232,Human_RBP_ID_26322556,Human_RBP_ID_27807538 Human_Splice_Rec_1447228,Human_Splice_Rec_1447229,Human_Splice_Rec_1447274,Human_Splice_Rec_1447275,Human_Splice_Rec_1447326,Human_Splice_Rec_1447327,Human_Splice_Rec_1447368 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_294782,RMVar_hsa_circ_60268,RMVar_hsa_circ_75106,RMVar_hsa_circ_161883,RMVar_hsa_circ_161884,RMVar_hsa_circ_302166,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_161885 96403 RMVar_ID_96403 Human_SNP_ID_521456506 m1A Human chr12 - 132784761 132784759 132784762 GCACATGTGCATGTGTGGTGTGGGGTGTGAACACGTGGGGTGTGAGCATGTGCGTGTGGGGTGTG GCACATGTGCATGTGTGGTGTGGGGTGTGAA___GTGGGGTGTGAGCATGTGCGTGTGGGGTGTG CGTG C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132784756..132784847 26863196 MeRIP-seq:(Medium) rs1566082453 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5283947,Human_RBP_ID_5644909,Human_RBP_ID_9352791,Human_RBP_ID_17242222,Human_RBP_ID_21967815,Human_RBP_ID_23582351 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_60268,RMVar_hsa_circ_75106,RMVar_hsa_circ_161884,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935 96404 RMVar_ID_96404 Human_SNP_ID_521457147 m1A Human chr12 + 132786666 132786666 132786666 CCCGGCCCCCGCACCTCCCACCTGGCCCCCGCACCTCCCCCGGGCACATGCAGACTTACTTCCGG CCCGGCCCCCGCACCTCCCACCTGGCCCCCGCCCCTCCCCCGGGCACATGCAGACTTACTTCCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132786663..132786733 26863196 MeRIP-seq:(Medium) rs774699084 Functional Loss SNV dbSNP153 33..33 33 - - - 96405 RMVar_ID_96405 Human_SNP_ID_521457148 m1A Human chr12 + 132786666 132786666 132786666 CCCGGCCCCCGCACCTCCCACCTGGCCCCCGCACCTCCCCCGGGCACATGCAGACTTACTTCCGG CCCGGCCCCCGCACCTCCCACCTGGCCCCCGCTCCTCCCCCGGGCACATGCAGACTTACTTCCGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132786663..132786733 26863196 MeRIP-seq:(Medium) rs774699084 Functional Loss SNV dbSNP153 33..33 33 - - - 96406 RMVar_ID_96406 Human_SNP_ID_521458183 m1A Human chr12 - 132788992 132788992 132788992 CTGTCCGTGTCGGGTTGACTCATTTGATGGGGAGGATTCGGCCAAAGTGCTTGTCGGGAGGGTGG CTGTCCGTGTCGGGTTGACTCATTTGATGGGGGGGATTCGGCCAAAGTGCTTGTCGGGAGGGTGG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132788990..132789091 26863196 MeRIP-seq:(Medium) rs549961676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19057311,Human_RBP_ID_22354632 RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_60268,RMVar_hsa_circ_112930,RMVar_hsa_circ_75106,RMVar_hsa_circ_161884,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_276536,RMVar_hsa_circ_375367,RMVar_hsa_circ_161888,RMVar_hsa_circ_1421,RMVar_hsa_circ_108679,RMVar_hsa_circ_161889,RMVar_hsa_circ_161890 96407 RMVar_ID_96407 Human_SNP_ID_521460789 m1A Human chr12 - 132796639 132796639 132796639 CATGCAGATTCAGGAGGCAAAGACGATGGTGGAGGAGGACCTTCAGAGGAGGCTGGAAGAGTTTG CATGCAGATTCAGGAGGCAAAGACGATGGTGGCGGAGGACCTTCAGAGGAGGCTGGAAGAGTTTG T G GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132796526..132796725 26863196 MeRIP-seq:(Medium) rs187924934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33729,Human_RBP_ID_228576,Human_RBP_ID_5521935,Human_RBP_ID_8779242,Human_RBP_ID_9255640,Human_RBP_ID_9279422,Human_RBP_ID_9367306,Human_RBP_ID_18410991,Human_RBP_ID_18978418,Human_RBP_ID_22910694,Human_RBP_ID_26322564,Human_RBP_ID_27806358 Human_Splice_Rec_1447216,Human_Splice_Rec_1447262,Human_Splice_Rec_1447314,Human_Splice_Rec_1447356 Human_miRNA_ID_2727959 RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_268395,RMVar_hsa_circ_58495,RMVar_hsa_circ_112930,RMVar_hsa_circ_75106,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_161888,RMVar_hsa_circ_1421,RMVar_hsa_circ_108679,RMVar_hsa_circ_161889,RMVar_hsa_circ_161891,RMVar_hsa_circ_51099,RMVar_hsa_circ_368670,RMVar_hsa_circ_333313,RMVar_hsa_circ_343335,RMVar_hsa_circ_354480,RMVar_hsa_circ_296106,RMVar_hsa_circ_127856,RMVar_hsa_circ_161892,RMVar_hsa_circ_161894,RMVar_hsa_circ_93790,RMVar_hsa_circ_161893 96408 RMVar_ID_96408 Human_SNP_ID_521464600 m1A Human chr12 - 132808352 132808352 132808352 CCGGCACATCCTAGGGAGAAAAAAACTTCCAAATCAAGCAAAATCCGGTCTCTGGCCGATTACAG CCGGCACATCCTAGGGAGAAAAAAACTTCCAAGTCAAGCAAAATCCGGTCTCTGGCCGATTACAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132808301..132808400 32194978 MeRIP-seq:(Medium) rs1310830094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33740,Human_RBP_ID_873465,Human_RBP_ID_1791218,Human_RBP_ID_17242223,Human_RBP_ID_22040744,Human_RBP_ID_26904640 RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_75106,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_161888,RMVar_hsa_circ_108679,RMVar_hsa_circ_161891,RMVar_hsa_circ_51099,RMVar_hsa_circ_368670,RMVar_hsa_circ_333313,RMVar_hsa_circ_343335,RMVar_hsa_circ_296106,RMVar_hsa_circ_72287,RMVar_hsa_circ_101119,RMVar_hsa_circ_127856,RMVar_hsa_circ_161892,RMVar_hsa_circ_161894,RMVar_hsa_circ_93790,RMVar_hsa_circ_355675,RMVar_hsa_circ_161893,RMVar_hsa_circ_326112,RMVar_hsa_circ_161898,RMVar_hsa_circ_161895,RMVar_hsa_circ_161896,RMVar_hsa_circ_104172,RMVar_hsa_circ_351290,RMVar_hsa_circ_354953,RMVar_hsa_circ_161897,RMVar_hsa_circ_370125,RMVar_hsa_circ_320947,RMVar_hsa_circ_93449,RMVar_hsa_circ_112338,RMVar_hsa_circ_161899,RMVar_hsa_circ_161900,RMVar_hsa_circ_276865,RMVar_hsa_circ_161901,RMVar_hsa_circ_161902,RMVar_hsa_circ_115208,RMVar_hsa_circ_161904,RMVar_hsa_circ_51000,RMVar_hsa_circ_161903 96409 RMVar_ID_96409 Human_SNP_ID_521466278 m1A Human chr12 - 132813330 132813330 132813330 GGAAGTGGCTGGAAGAGCAGCTCAAACAGTACAGGGTGAAGCGCCAGCAGGAGAGGGTGAGTCTC GGAAGTGGCTGGAAGAGCAGCTCAAACAGTACCGGGTGAAGCGCCAGCAGGAGAGGGTGAGTCTC T G GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132808484..132813425 32194978 MeRIP-seq:(Medium) rs1453561887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_878218,Human_RBP_ID_3942621,Human_RBP_ID_5521941,Human_RBP_ID_9365979 Human_Splice_Rec_1447204,Human_Splice_Rec_1447205,Human_Splice_Rec_1447250,Human_Splice_Rec_1447251,Human_Splice_Rec_1447302,Human_Splice_Rec_1447303,Human_Splice_Rec_1447344,Human_Splice_Rec_1447345 Human_miRNA_ID_75599,Human_miRNA_ID_78769,Human_miRNA_ID_1950742,Human_miRNA_ID_1952029,Human_miRNA_ID_2512354,Human_miRNA_ID_2717518,Human_miRNA_ID_3055177 RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_13296,RMVar_hsa_circ_75106,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_161888,RMVar_hsa_circ_108679,RMVar_hsa_circ_161891,RMVar_hsa_circ_51099,RMVar_hsa_circ_368670,RMVar_hsa_circ_333313,RMVar_hsa_circ_296106,RMVar_hsa_circ_101119,RMVar_hsa_circ_161892,RMVar_hsa_circ_161894,RMVar_hsa_circ_93790,RMVar_hsa_circ_326112,RMVar_hsa_circ_161898,RMVar_hsa_circ_161895,RMVar_hsa_circ_161896,RMVar_hsa_circ_104172,RMVar_hsa_circ_351290,RMVar_hsa_circ_354953,RMVar_hsa_circ_161897,RMVar_hsa_circ_370125,RMVar_hsa_circ_320947,RMVar_hsa_circ_93449,RMVar_hsa_circ_112338,RMVar_hsa_circ_161899,RMVar_hsa_circ_161900,RMVar_hsa_circ_276865,RMVar_hsa_circ_161901,RMVar_hsa_circ_161902,RMVar_hsa_circ_161904,RMVar_hsa_circ_51000,RMVar_hsa_circ_310624 96410 RMVar_ID_96410 Human_SNP_ID_521470540 m1A Human chr12 + 132825720 132825720 132825720 AGTGGCCGGGAAGATGGCGGACATTCAGACTGAGCGTGCCTACCAAAAGCAGCCGACCATCTTTC AGTGGCCGGGAAGATGGCGGACATTCAGACTGTGCGTGCCTACCAAAAGCAGCCGACCATCTTTC A T RPS11P5 Ensembl:ENSG00000232888 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1566155736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415613,Human_RBP_ID_1468547,Human_RBP_ID_1791234,Human_RBP_ID_3398937,Human_RBP_ID_5173018,Human_RBP_ID_5491253,Human_RBP_ID_6155300,Human_RBP_ID_8370530,Human_RBP_ID_8779275,Human_RBP_ID_11885164,Human_RBP_ID_17237255,Human_RBP_ID_17353157,Human_RBP_ID_18511582,Human_RBP_ID_18622790,Human_RBP_ID_23549237,Human_RBP_ID_24406738,Human_RBP_ID_24464893 Human_miRNA_ID_1853120,Human_miRNA_ID_1863613,Human_miRNA_ID_1895925 96411 RMVar_ID_96411 Human_SNP_ID_521470546 m1A Human chr12 + 132825729 132825729 132825729 GAAGATGGCGGACATTCAGACTGAGCGTGCCTACCAAAAGCAGCCGACCATCTTTCAAAACAAGA GAAGATGGCGGACATTCAGACTGAGCGTGCCTCCCAAAAGCAGCCGACCATCTTTCAAAACAAGA A C RPS11P5 Ensembl:ENSG00000232888 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1398641006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415613,Human_RBP_ID_1468547,Human_RBP_ID_1791234,Human_RBP_ID_3398937,Human_RBP_ID_5173018,Human_RBP_ID_5491253,Human_RBP_ID_8370530,Human_RBP_ID_11885164,Human_RBP_ID_17237255,Human_RBP_ID_17353157,Human_RBP_ID_18511582,Human_RBP_ID_18622790,Human_RBP_ID_23549237 Human_miRNA_ID_1853120,Human_miRNA_ID_1863613 96412 RMVar_ID_96412 Human_SNP_ID_521471480 m1A Human chr12 + 132828646 132828646 132828646 GGCGGGCGCCCAGGCCCGAGGCCACCGCAGCGAGGCGGGGGTGACTGGAACGGGGCCGTCCCGCC GGCGGGCGCCCAGGCCCGAGGCCACCGCAGCGCGGCGGGGGTGACTGGAACGGGGCCGTCCCGCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:132828600..132828794 26863196 MeRIP-seq:(Medium) rs1000896898 Functional Loss SNV dbSNP153 33..33 33 - - - 96413 RMVar_ID_96413 Human_SNP_ID_521474789 m1A Human chr12 + 132839507 132839507 132839507 AAGGACCTCCCCTCTCAGCCTCGCCTCTGCACAAACTCAGGACCTCCCCTCTCGGCCTCACCCCC AAGGACCTCCCCTCTCAGCCTCGCCTCTGCACTAACTCAGGACCTCCCCTCTCGGCCTCACCCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132839457..132839577 26863196 MeRIP-seq:(Medium) rs1456049142 Functional Loss SNV dbSNP153 33..33 33 - - - 96414 RMVar_ID_96414 Human_SNP_ID_521474901 m1A Human chr12 - 132839810 132839810 132839810 CCGAGTTTGTGCAGGGGCGAGGCTGAGAGGGGAGGTCCCTAGTTAGTGCAGGGGTGAGGCCGAGA CCGAGTTTGTGCAGGGGCGAGGCTGAGAGGGGTGGTCCCTAGTTAGTGCAGGGGTGAGGCCGAGA T A CHFR Ensembl:ENSG00000072609 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132839775..132839912 26863196 MeRIP-seq:(Medium) rs1171600400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8177804,Human_RBP_ID_26777721 96415 RMVar_ID_96415 Human_SNP_ID_521504025 m1A Human chr12 - 132941808 132941779 132941808 TGATGGAGGGCAGCCTCGAGAAGGAGCGTGACAGAGGGCAGCCTGGAAAAGGGCGCGTGACGGAG TGATGGAGGGCAGCCTCGAGAAGGAGCGTGAC_____________________________GGAG CGTCACGCGCCCTTTTCCAGGCTGCCCTCT C CHFR,ZNF605 Ensembl:ENSG00000072609,Ensembl:ENSG00000196458 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132941757..132941905 26863196 MeRIP-seq:(Medium) rs1460792334 Functional Loss DEL dbSNP153 33..61 33 - - - RMVar_hsa_circ_318891,RMVar_hsa_circ_290766 96416 RMVar_ID_96416 Human_SNP_ID_521504036 m1A Human chr12 - 132941808 132941808 132941808 TGATGGAGGGCAGCCTCGAGAAGGAGCGTGACAGAGGGCAGCCTGGAAAAGGGCGCGTGACGGAG TGATGGAGGGCAGCCTCGAGAAGGAGCGTGACGGAGGGCAGCCTGGAAAAGGGCGCGTGACGGAG T C CHFR,ZNF605 Ensembl:ENSG00000072609,Ensembl:ENSG00000196458 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132941757..132941905 26863196 MeRIP-seq:(Medium) rs56382327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318891,RMVar_hsa_circ_290766 96417 RMVar_ID_96417 Human_SNP_ID_521507095 m1A Human chr12 + 132953857 132953857 132953857 CTCACCCTCACCCACCCGCACACCCATCACAGACACTTGCACGCATACTTGGCATTGATCCCAAG CTCACCCTCACCCACCCGCACACCCATCACAGGCACTTGCACGCATACTTGGCATTGATCCCAAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:132953757..132953886 26863196 MeRIP-seq:(Medium) rs1345872182 Functional Loss SNV dbSNP153 33..33 33 - - - 96418 RMVar_ID_96418 Human_SNP_ID_521507109 m1A Human chr12 + 132953910 132953910 132953910 ATTGATCCCAAGCCCTCCGATCATTCCTCCTCACAGACCTCACTGCCCACCCCATCAGTCATTCA ATTGATCCCAAGCCCTCCGATCATTCCTCCTCGCAGACCTCACTGCCCACCCCATCAGTCATTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132953903..132954114 26863196 MeRIP-seq:(Medium) rs1207275682 Functional Loss SNV dbSNP153 33..33 33 - - - 96419 RMVar_ID_96419 Human_SNP_ID_521525735 m1A Human chr12 - 133037547 133037547 133037547 AGCGCCGGGCCCGCAATAAACTCACTGAACTCACAAAAGACGCCGCCGCCGAGTCGCGCCCGCGC AGCGCCGGGCCCGCAATAAACTCACTGAACTCCCAAAAGACGCCGCCGCCGAGTCGCGCCCGCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:133037328..133037763;chr12:133037353..133037801 26863196 MeRIP-seq:(Medium) rs926578602 Functional Loss SNV dbSNP153 33..33 33 - - - 96420 RMVar_ID_96420 Human_SNP_ID_521525787 m1A Human chr12 + 133037663 133037654 133037664 TCGGCTTCAAGGCCCTGGGCGTCCGCGCGCGGATGCGGGTCTGGGGCGGGTTGGGGCTGGGCCGG TCGGCTTCAAGGCCCTGGGCGTCC__________GCGGGTCTGGGGCGGGTTGGGGCTGGGCCGG CGCGCGCGGAT C ZNF84 Ensembl:ENSG00000198040 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:133037643..133037750 26863196 MeRIP-seq:(Medium) rs1387420947 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_5348003,Human_RBP_ID_9416369,Human_RBP_ID_17112523,Human_RBP_ID_19057327,Human_RBP_ID_21967338,Human_RBP_ID_27836895 96421 RMVar_ID_96421 Human_SNP_ID_521528390 m1A Human chr12 - 133048934 133048934 133048934 CACTGACCAGCCAACCCATCACTGACCAGCCCACCCATCACTGACTAGCCCACCCGTCACTGACC CACTGACCAGCCAACCCATCACTGACCAGCCCGCCCATCACTGACTAGCCCACCCGTCACTGACC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:133048875..133048999 26863196 MeRIP-seq:(Medium) rs1232185140 Functional Loss SNV dbSNP153 33..33 33 - - - 96422 RMVar_ID_96422 Human_SNP_ID_521548380 m1A Human chr12 + 133130211 133130211 133130211 CACGAGGGACTTGTCCCGGGTGAACGAGCCACAGGCCCGCATGCTCACCCGTCCTCAGTGCCTGC CACGAGGGACTTGTCCCGGGTGAACGAGCCACGGGCCCGCATGCTCACCCGTCCTCAGTGCCTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:133130185..133130256 26863196 MeRIP-seq:(Medium) rs1269992742 Functional Loss SNV dbSNP153 33..33 33 - - - 96423 RMVar_ID_96423 Human_SNP_ID_579547558 m1A Human chr15 + 60005900 60005900 60005900 AAAGCAGCCCCGCCACCCCCAGCGAAACGCTCACCAGCCCGGCCTCCGCCTTGCACTCGGTGGCG AAAGCAGCCCCGCCACCCCCAGCGAAACGCTCCCCAGCCCGGCCTCCGCCTTGCACTCGGTGGCG A C FOXB1 Ensembl:ENSG00000171956 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60005824..60006006 26863196 MeRIP-seq:(Medium) rs1339266226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27232566 96424 RMVar_ID_96424 Human_SNP_ID_579646861 m1A Human chr15 - 60357238 60357238 60357238 TTCCCTGCTGATGTTCGTGCTTCCTGGTTCACAGGGGCTGGGAACCGACGAGGACTCTCTCATTG TTCCCTGCTGATGTTCGTGCTTCCTGGTTCACGGGGGCTGGGAACCGACGAGGACTCTCTCATTG T C ANXA2 Ensembl:ENSG00000182718 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60357219..60357293 26863196 MeRIP-seq:(Medium) rs758715993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886595,Human_RBP_ID_22439816,Human_RBP_ID_22649954 Human_Splice_Rec_1608749,Human_Splice_Rec_1608773,Human_Splice_Rec_1608797,Human_Splice_Rec_1608817,Human_Splice_Rec_1608837,Human_Splice_Rec_1608861,Human_Splice_Rec_1608883,Human_Splice_Rec_1608901,Human_Splice_Rec_1608915,Human_Splice_Rec_1608933,Human_Splice_Rec_1608947,Human_Splice_Rec_1608967,Human_Splice_Rec_1608985,Human_Splice_Rec_1609005,Human_Splice_Rec_1609017,Human_Splice_Rec_1609031,Human_Splice_Rec_1609043,Human_Splice_Rec_1609057,Human_Splice_Rec_1609069,Human_Splice_Rec_1609085,Human_Splice_Rec_1609097 RMVar_hsa_circ_93056,RMVar_hsa_circ_51075,RMVar_hsa_circ_111674,RMVar_hsa_circ_289444,RMVar_hsa_circ_42634,RMVar_hsa_circ_124678,RMVar_hsa_circ_172544,RMVar_hsa_circ_374625,RMVar_hsa_circ_172543,RMVar_hsa_circ_345252,RMVar_hsa_circ_96765,RMVar_hsa_circ_172549,RMVar_hsa_circ_6297,RMVar_hsa_circ_172550,RMVar_hsa_circ_172548,RMVar_hsa_circ_172551,RMVar_hsa_circ_105218,RMVar_hsa_circ_52898,RMVar_hsa_circ_172552,RMVar_hsa_circ_85379,RMVar_hsa_circ_172553,RMVar_hsa_circ_125815,RMVar_hsa_circ_322584,RMVar_hsa_circ_371075,RMVar_hsa_circ_172556,RMVar_hsa_circ_282085,RMVar_hsa_circ_172557,RMVar_hsa_circ_325479,RMVar_hsa_circ_278214,RMVar_hsa_circ_172559,RMVar_hsa_circ_172560,RMVar_hsa_circ_326773,RMVar_hsa_circ_367664,RMVar_hsa_circ_172558,RMVar_hsa_circ_367469,RMVar_hsa_circ_172561,RMVar_hsa_circ_172562 96425 RMVar_ID_96425 Human_SNP_ID_579646862 m1A Human chr15 - 60357238 60357238 60357238 TTCCCTGCTGATGTTCGTGCTTCCTGGTTCACAGGGGCTGGGAACCGACGAGGACTCTCTCATTG TTCCCTGCTGATGTTCGTGCTTCCTGGTTCACCGGGGCTGGGAACCGACGAGGACTCTCTCATTG T G ANXA2 Ensembl:ENSG00000182718 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60357219..60357293 26863196 MeRIP-seq:(Medium) rs758715993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886595,Human_RBP_ID_22439816,Human_RBP_ID_22649954 Human_Splice_Rec_1608749,Human_Splice_Rec_1608773,Human_Splice_Rec_1608797,Human_Splice_Rec_1608817,Human_Splice_Rec_1608837,Human_Splice_Rec_1608861,Human_Splice_Rec_1608883,Human_Splice_Rec_1608901,Human_Splice_Rec_1608915,Human_Splice_Rec_1608933,Human_Splice_Rec_1608947,Human_Splice_Rec_1608967,Human_Splice_Rec_1608985,Human_Splice_Rec_1609005,Human_Splice_Rec_1609017,Human_Splice_Rec_1609031,Human_Splice_Rec_1609043,Human_Splice_Rec_1609057,Human_Splice_Rec_1609069,Human_Splice_Rec_1609085,Human_Splice_Rec_1609097 RMVar_hsa_circ_93056,RMVar_hsa_circ_51075,RMVar_hsa_circ_111674,RMVar_hsa_circ_289444,RMVar_hsa_circ_42634,RMVar_hsa_circ_124678,RMVar_hsa_circ_172544,RMVar_hsa_circ_374625,RMVar_hsa_circ_172543,RMVar_hsa_circ_345252,RMVar_hsa_circ_96765,RMVar_hsa_circ_172549,RMVar_hsa_circ_6297,RMVar_hsa_circ_172550,RMVar_hsa_circ_172548,RMVar_hsa_circ_172551,RMVar_hsa_circ_105218,RMVar_hsa_circ_52898,RMVar_hsa_circ_172552,RMVar_hsa_circ_85379,RMVar_hsa_circ_172553,RMVar_hsa_circ_125815,RMVar_hsa_circ_322584,RMVar_hsa_circ_371075,RMVar_hsa_circ_172556,RMVar_hsa_circ_282085,RMVar_hsa_circ_172557,RMVar_hsa_circ_325479,RMVar_hsa_circ_278214,RMVar_hsa_circ_172559,RMVar_hsa_circ_172560,RMVar_hsa_circ_326773,RMVar_hsa_circ_367664,RMVar_hsa_circ_172558,RMVar_hsa_circ_367469,RMVar_hsa_circ_172561,RMVar_hsa_circ_172562 96426 RMVar_ID_96426 Human_SNP_ID_579654542 m1A Human chr15 - 60382401 60382401 60382401 ACCCCCAAGTGCATATGGGTCTGTCAAAGCCTATACTAACTTTGATGCTGAGCGGGATGCTTTGA ACCCCCAAGTGCATATGGGTCTGTCAAAGCCTGTACTAACTTTGATGCTGAGCGGGATGCTTTGA T C ANXA2 Ensembl:ENSG00000182718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60382360..60382431 26863196 MeRIP-seq:(Medium) rs747064927 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4326687,Human_RBP_ID_18189562,Human_RBP_ID_22440634,Human_RBP_ID_27435841 Human_Splice_Rec_1608742,Human_Splice_Rec_1608743,Human_Splice_Rec_1608766,Human_Splice_Rec_1608767,Human_Splice_Rec_1608790,Human_Splice_Rec_1608791,Human_Splice_Rec_1608811,Human_Splice_Rec_1608830,Human_Splice_Rec_1608831,Human_Splice_Rec_1608854,Human_Splice_Rec_1608855,Human_Splice_Rec_1608926,Human_Splice_Rec_1608927,Human_Splice_Rec_1608958,Human_Splice_Rec_1608959,Human_Splice_Rec_1608978,Human_Splice_Rec_1608979,Human_Splice_Rec_1608998,Human_Splice_Rec_1608999,Human_Splice_Rec_1609024,Human_Splice_Rec_1609025,Human_Splice_Rec_1609036,Human_Splice_Rec_1609037,Human_Splice_Rec_1609050,Human_Splice_Rec_1609051,Human_Splice_Rec_1609078,Human_Splice_Rec_1609079,Human_Splice_Rec_1609104,Human_Splice_Rec_1609105,Human_Splice_Rec_1609116,Human_Splice_Rec_1609117,Human_Splice_Rec_1609128,Human_Splice_Rec_1609129,Human_Splice_Rec_1609144,Human_Splice_Rec_1609145,Human_Splice_Rec_1609154,Human_Splice_Rec_1609155,Human_Splice_Rec_1609164,Human_Splice_Rec_1609165,Human_Splice_Rec_1609174,Human_Splice_Rec_1609175,Human_Splice_Rec_1609190,Human_Splice_Rec_1609191,Human_Splice_Rec_1609198,Human_Splice_Rec_1609199,Human_Splice_Rec_1609208,Human_Splice_Rec_1609209,Human_Splice_Rec_1609218 RMVar_hsa_circ_93056,RMVar_hsa_circ_51075,RMVar_hsa_circ_111674,RMVar_hsa_circ_124678,RMVar_hsa_circ_374625,RMVar_hsa_circ_172543,RMVar_hsa_circ_96765,RMVar_hsa_circ_172549,RMVar_hsa_circ_6297,RMVar_hsa_circ_172550,RMVar_hsa_circ_172551,RMVar_hsa_circ_2198,RMVar_hsa_circ_105218,RMVar_hsa_circ_52898,RMVar_hsa_circ_172552,RMVar_hsa_circ_322584,RMVar_hsa_circ_282085,RMVar_hsa_circ_325479,RMVar_hsa_circ_172559,RMVar_hsa_circ_172560,RMVar_hsa_circ_326773,RMVar_hsa_circ_367664,RMVar_hsa_circ_172561,RMVar_hsa_circ_172563,RMVar_hsa_circ_47446,RMVar_hsa_circ_273183,RMVar_hsa_circ_172562,RMVar_hsa_circ_292240,RMVar_hsa_circ_172564,RMVar_hsa_circ_114795,RMVar_hsa_circ_172567,RMVar_hsa_circ_307579,RMVar_hsa_circ_346419,RMVar_hsa_circ_172568,RMVar_hsa_circ_292600,RMVar_hsa_circ_277326,RMVar_hsa_circ_117179,RMVar_hsa_circ_91465,RMVar_hsa_circ_172570,RMVar_hsa_circ_172571,RMVar_hsa_circ_172572,RMVar_hsa_circ_172569 96427 RMVar_ID_96427 Human_SNP_ID_579654543 m1A Human chr15 + 60382402 60382402 60382402 CAAAGCATCCCGCTCAGCATCAAAGTTAGTATAGGCTTTGACAGACCCATATGCACTTGGGGGTG CAAAGCATCCCGCTCAGCATCAAAGTTAGTATGGGCTTTGACAGACCCATATGCACTTGGGGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:60382351..60382453 32194978 MeRIP-seq:(Medium) rs1263497771 Functional Loss SNV dbSNP153 33..33 33 - - - 96428 RMVar_ID_96428 Human_SNP_ID_579654687 m1A Human chr15 + 60382915 60382915 60382915 CTGAGCTTACAATTCAGATAAATGAGGGAAGCAGCTTCTCCCACCTCTTTACTTTGGTCACCACT CTGAGCTTACAATTCAGATAAATGAGGGAAGCGGCTTCTCCCACCTCTTTACTTTGGTCACCACT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:60382875..60383117 26863196 MeRIP-seq:(Medium) rs995434982 Functional Loss SNV dbSNP153 33..33 33 - - - 96429 RMVar_ID_96429 Human_SNP_ID_579658609 m1A Human chr15 + 60397754 60397754 60397754 CCCGAGGGCCGGTGGCCCCTCACCCCTGCCCCAAACACCTTGTCCCTGAGCCCCCTCCCCAAAGA CCCGAGGGCCGGTGGCCCCTCACCCCTGCCCCCAACACCTTGTCCCTGAGCCCCCTCCCCAAAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr15:60397751..60397959;chr15:60397738..60397899 26863196 MeRIP-seq:(Medium) rs1365100072 Functional Loss SNV dbSNP153 33..33 33 - - - 96430 RMVar_ID_96430 Human_SNP_ID_579660920 m1A Human chr15 + 60404634 60404634 60404634 AGGCCATGCAGTCTCTCAAGTCCCGAGGCTACATGAAGGAACAGTTTGCCTGGAGACATTTCTAC AGGCCATGCAGTCTCTCAAGTCCCGAGGCTACGTGAAGGAACAGTTTGCCTGGAGACATTTCTAC A G AC087385.2 Ensembl:ENSG00000242667 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1183249559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1839304 96431 RMVar_ID_96431 Human_SNP_ID_579681784 m1A Human chr15 - 60478066 60478063 60478067 TTTGATCTTGGCCTTTTGTTTTTACTCAGCTGAGTAAGTTCTGGAGGGATCCTGCCTCTTGGAGC TTTGATCTTGGCCTTTTGTTTTTACTCAGCT____AAGTTCTGGAGGGATCCTGCCTCTTGGAGC TACTC T ICE2 Ensembl:ENSG00000128915 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:60478016..60478138 26863196 MeRIP-seq:(Medium) rs1361102134 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3945550,Human_RBP_ID_4326759,Human_RBP_ID_8803860,Human_RBP_ID_9370994,Human_RBP_ID_18981521,Human_RBP_ID_25149400,Human_RBP_ID_26326805 Human_Splice_Rec_1609234,Human_Splice_Rec_1609264,Human_Splice_Rec_1609316,Human_Splice_Rec_1609332,Human_Splice_Rec_1609350,Human_Splice_Rec_1609366,Human_Splice_Rec_1609388,Human_Splice_Rec_1609396,Human_Splice_Rec_1609406,Human_Splice_Rec_1609414 RMVar_hsa_circ_8346,RMVar_hsa_circ_378962,RMVar_hsa_circ_73564,RMVar_hsa_circ_61667 96432 RMVar_ID_96432 Human_SNP_ID_579682138 m1A Human chr15 + 60479049 60479049 60479049 CGGCTCTTGCCCAGGCCGCAGCCACACACCACACACGCTCCACCCCACTCCTCACATTGTCGCGC CGGCTCTTGCCCAGGCCGCAGCCACACACCACGCACGCTCCACCCCACTCCTCACATTGTCGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:60478944..60479102;chr15:60478899..60479100;chr15:60478948..60479088 26863196 MeRIP-seq:(Medium) rs994082510 Functional Loss SNV dbSNP153 33..33 33 - - - 96433 RMVar_ID_96433 Human_SNP_ID_579682141 m1A Human chr15 + 60479051 60479051 60479051 GCTCTTGCCCAGGCCGCAGCCACACACCACACACGCTCCACCCCACTCCTCACATTGTCGCGCGC GCTCTTGCCCAGGCCGCAGCCACACACCACACGCGCTCCACCCCACTCCTCACATTGTCGCGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:60478900..60479107 26863196 MeRIP-seq:(Medium) rs778642816 Functional Loss SNV dbSNP153 33..33 33 - - - 96434 RMVar_ID_96434 Human_SNP_ID_579682274 m1A Human chr15 - 60479246 60479246 60479246 GCAGTCTCCAACCACTTCCGCCTGGCGAGCCCAGTCTCGCACTTCGCTGCCAGAACCACAGCGAG GCAGTCTCCAACCACTTCCGCCTGGCGAGCCCTGTCTCGCACTTCGCTGCCAGAACCACAGCGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60479230..60479337 26863196 MeRIP-seq:(Medium) rs929789046 Functional Loss SNV dbSNP153 33..33 33 - - - 96435 RMVar_ID_96435 Human_SNP_ID_579682275 m1A Human chr15 - 60479246 60479246 60479246 GCAGTCTCCAACCACTTCCGCCTGGCGAGCCCAGTCTCGCACTTCGCTGCCAGAACCACAGCGAG GCAGTCTCCAACCACTTCCGCCTGGCGAGCCCGGTCTCGCACTTCGCTGCCAGAACCACAGCGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60479230..60479337 26863196 MeRIP-seq:(Medium) rs929789046 Functional Loss SNV dbSNP153 33..33 33 - - - 96436 RMVar_ID_96436 Human_SNP_ID_579871737 m1A Human chr15 - 61229136 61229136 61229136 CAGCGGCGCGGACGCGGCCGCCGGCTCCAGGGAGACCCCGCTGAACCAGGAATCCGCCCGCAAGA CAGCGGCGCGGACGCGGCCGCCGGCTCCAGGGTGACCCCGCTGAACCAGGAATCCGCCCGCAAGA T A RORA Ensembl:ENSG00000069667 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:61229097..61229189 26863410 MeRIP-seq:(Medium) rs1217012259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1609463,Human_Splice_Rec_1609547,Human_Splice_Rec_1609573,Human_Splice_Rec_1609577,Human_Splice_Rec_1609583,Human_Splice_Rec_1609585,Human_Splice_Rec_1609589 96437 RMVar_ID_96437 Human_SNP_ID_579871738 m1A Human chr15 - 61229136 61229136 61229136 CAGCGGCGCGGACGCGGCCGCCGGCTCCAGGGAGACCCCGCTGAACCAGGAATCCGCCCGCAAGA CAGCGGCGCGGACGCGGCCGCCGGCTCCAGGGCGACCCCGCTGAACCAGGAATCCGCCCGCAAGA T G RORA Ensembl:ENSG00000069667 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:61229097..61229189 26863410 MeRIP-seq:(Medium) rs1217012259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1609463,Human_Splice_Rec_1609547,Human_Splice_Rec_1609573,Human_Splice_Rec_1609577,Human_Splice_Rec_1609583,Human_Splice_Rec_1609585,Human_Splice_Rec_1609589 96438 RMVar_ID_96438 Human_SNP_ID_580036725 m1A Human chr15 + 61869601 61869601 61869601 ACAAGCCCTTTTCCAATTCCTTTAAAGAATCCAGCAGCTCCTTCCTTTTTGGCACCTTCAGAAAA ACAAGCCCTTTTCCAATTCCTTTAAAGAATCCGGCAGCTCCTTCCTTTTTGGCACCTTCAGAAAA A G AC009554.1,AC009554.2 Ensembl:ENSG00000259564,Ensembl:ENSG00000285863 lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:61869564..61869698 26863196 MeRIP-seq:(Medium) rs1209532003 Functional Loss SNV dbSNP153 33..33 33 - - - 96439 RMVar_ID_96439 Human_SNP_ID_580037566 m1A Human chr15 + 61873144 61873144 61873144 GAAGTCCATCATTTATCATTCTTTCTATTCCTACAGGCCTAGACTCATAAGCAGCATTCTAAGTT GAAGTCCATCATTTATCATTCTTTCTATTCCTGCAGGCCTAGACTCATAAGCAGCATTCTAAGTT A G AC009554.1,AC009554.2 Ensembl:ENSG00000259564,Ensembl:ENSG00000285863 lincRNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:61873143..61873275 26863196 MeRIP-seq:(Medium) rs1171058947 Functional Loss SNV dbSNP153 33..33 33 - - - 96440 RMVar_ID_96440 Human_SNP_ID_580092126 m1A Human chr15 - 62068062 62068062 62068062 CCGCGGGGGTCGCCGGGCCCGGAGCTCGCGGGACGCGCAGGGTCCCCAGGAGGGCGTCCGGGCCG CCGCGGGGGTCGCCGGGCCCGGAGCTCGCGGGCCGCGCAGGGTCCCCAGGAGGGCGTCCGGGCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:62068015..62068110 26863196 MeRIP-seq:(Medium) rs12912898 Functional Loss SNV dbSNP153 33..33 33 - - - 96441 RMVar_ID_96441 Human_SNP_ID_580179856 m1A Human chr15 + 62390629 62390629 62390629 GGGAGCGGAGTGGTCGCCCAGCGCGCGGGGGGACGCGGGCTGCACTCCCGGGCAGGCGCTCTGCA GGGAGCGGAGTGGTCGCCCAGCGCGCGGGGGGGCGCGGGCTGCACTCCCGGGCAGGCGCTCTGCA A G TLN2 Ensembl:ENSG00000171914 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:62390583..62390744 26863196 MeRIP-seq:(Medium) rs1006096442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343152,Human_RBP_ID_18418476,Human_RBP_ID_22934772 Human_Splice_Rec_1610615 96442 RMVar_ID_96442 Human_SNP_ID_580283594 m1A Human chr15 - 62764930 62764930 62764930 TCTCGCTCTGTTGTCCCAGGCTTAAGGGCGGCAGTGTGATCTCGGCTCACTCACTGCACTCTCCG TCTCGCTCTGTTGTCCCAGGCTTAAGGGCGGCCGTGTGATCTCGGCTCACTCACTGCACTCTCCG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:62764916..62765045 26863196 MeRIP-seq:(Medium) rs1386804068 Functional Loss SNV dbSNP153 33..33 33 - - - 96443 RMVar_ID_96443 Human_SNP_ID_580359367 m1A Human chr15 - 63042764 63042764 63042764 AGGAGCGGCGGGGCGAGCGCGCGGTCGGGCGGAGGAGCGGGAGTGCGAGCGCGGAGCCGCCTGCT AGGAGCGGCGGGGCGAGCGCGCGGTCGGGCGGGGGAGCGGGAGTGCGAGCGCGGAGCCGCCTGCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:63042726..63042866 26863196 MeRIP-seq:(Medium) rs193170738 Functional Loss SNV dbSNP153 33..33 33 - - - 96444 RMVar_ID_96444 Human_SNP_ID_580359368 m1A Human chr15 - 63042764 63042764 63042764 AGGAGCGGCGGGGCGAGCGCGCGGTCGGGCGGAGGAGCGGGAGTGCGAGCGCGGAGCCGCCTGCT AGGAGCGGCGGGGCGAGCGCGCGGTCGGGCGGCGGAGCGGGAGTGCGAGCGCGGAGCCGCCTGCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:63042726..63042866 26863196 MeRIP-seq:(Medium) rs193170738 Functional Loss SNV dbSNP153 33..33 33 - - - 96445 RMVar_ID_96445 Human_SNP_ID_580359416 m1A Human chr15 - 63042852 63042852 63042852 AGGCGTTCTCCTTGTCGAGCTTCAGCATCTGCATCTTCTTCTTGATGGCGTCCATGGTGGCGGCG AGGCGTTCTCCTTGTCGAGCTTCAGCATCTGCCTCTTCTTCTTGATGGCGTCCATGGTGGCGGCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:63042801..63042900 32194978 MeRIP-seq:(Medium) rs397516364 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_559 GWAS_ID_12658,GWAS_ID_12659 96446 RMVar_ID_96446 Human_SNP_ID_580359445 m1A Human chr15 + 63042906 63042906 63042906 GGAGAACGCCTTGGATCGAGCTGAGCAGGCGGAGGCCGACAAGAAGGCGGCGGAAGACAGGAGCA GGAGAACGCCTTGGATCGAGCTGAGCAGGCGGGGGCCGACAAGAAGGCGGCGGAAGACAGGAGCA A G TPM1 Ensembl:ENSG00000140416 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:63042681..63042994 26863196 MeRIP-seq:(Medium) rs730880234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371673,Human_RBP_ID_18665282 Human_Splice_Rec_1610981,Human_Splice_Rec_1610999,Human_Splice_Rec_1611027,Human_Splice_Rec_1611043,Human_Splice_Rec_1611045,Human_Splice_Rec_1611063,Human_Splice_Rec_1611081,Human_Splice_Rec_1611085,Human_Splice_Rec_1611095,Human_Splice_Rec_1611109,Human_Splice_Rec_1611125,Human_Splice_Rec_1611141,Human_Splice_Rec_1611157,Human_Splice_Rec_1611175 Clinvar_Rec_560 96447 RMVar_ID_96447 Human_SNP_ID_580359464 m1A Human chr15 + 63042935 63042935 63042935 CGGAGGCCGACAAGAAGGCGGCGGAAGACAGGAGCAAGCAGGTCTGCGCCTCCCCGGCCCTGCGC CGGAGGCCGACAAGAAGGCGGCGGAAGACAGGGGCAAGCAGGTCTGCGCCTCCCCGGCCCTGCGC A G TPM1 Ensembl:ENSG00000140416 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63042651..63043075 26863196 MeRIP-seq:(Medium) rs1566936237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371673 Human_Splice_Rec_1610981,Human_Splice_Rec_1610999,Human_Splice_Rec_1611027,Human_Splice_Rec_1611043,Human_Splice_Rec_1611045,Human_Splice_Rec_1611063,Human_Splice_Rec_1611081,Human_Splice_Rec_1611085,Human_Splice_Rec_1611095,Human_Splice_Rec_1611109,Human_Splice_Rec_1611125,Human_Splice_Rec_1611141,Human_Splice_Rec_1611157,Human_Splice_Rec_1611175 Clinvar_Rec_561 96448 RMVar_ID_96448 Human_SNP_ID_580359469 m1A Human chr15 - 63042945 63042945 63042945 CTGGGCGCGGGCGCAGGGCCGGGGAGGCGCAGACCTGCTTGCTCCTGTCTTCCGCCGCCTTCTTG CTGGGCGCGGGCGCAGGGCCGGGGAGGCGCAGGCCTGCTTGCTCCTGTCTTCCGCCGCCTTCTTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:63042926..63042950 32194978 MeRIP-seq:(Medium) rs1114167357 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_562,Clinvar_Rec_5373 96449 RMVar_ID_96449 Human_SNP_ID_580359891 m1A Human chr15 + 63044076 63044076 63044076 GTCACTGCAAAAGAAACTCAAGGGCACCGAAGATGAACTGGACAAATACTCTGAGGCTCTCAAAG GTCACTGCAAAAGAAACTCAAGGGCACCGAAGGTGAACTGGACAAATACTCTGAGGCTCTCAAAG A G TPM1 Ensembl:ENSG00000140416 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:63044026..63044075 32194978 MeRIP-seq:(Medium) rs1566937759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1831494,Human_RBP_ID_9371005 Human_Splice_Rec_1610982,Human_Splice_Rec_1610983,Human_Splice_Rec_1611000,Human_Splice_Rec_1611001,Human_Splice_Rec_1611028,Human_Splice_Rec_1611029,Human_Splice_Rec_1611044,Human_Splice_Rec_1611046,Human_Splice_Rec_1611047,Human_Splice_Rec_1611066,Human_Splice_Rec_1611067,Human_Splice_Rec_1611087,Human_Splice_Rec_1611096,Human_Splice_Rec_1611097,Human_Splice_Rec_1611110,Human_Splice_Rec_1611111,Human_Splice_Rec_1611176,Human_Splice_Rec_1611177,Human_Splice_Rec_1611193,Human_Splice_Rec_1611209 Human_miRNA_ID_311458,Human_miRNA_ID_2071018,Human_miRNA_ID_2803938 Clinvar_Rec_563 RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_172694 96450 RMVar_ID_96450 Human_SNP_ID_580360831 m1A Human chr15 + 63048137 63048137 63048137 TCTGGACTCGGGAGCGGAGCGCTCCCGCGGCCAGCAGGAGTCGCTATTGCCCTTAGCAGCCAGCT TCTGGACTCGGGAGCGGAGCGCTCCCGCGGCCCGCAGGAGTCGCTATTGCCCTTAGCAGCCAGCT A C TPM1 Ensembl:ENSG00000140416 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63048130..63048352 26863196 MeRIP-seq:(Medium) rs898627357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_172694 96451 RMVar_ID_96451 Human_SNP_ID_580360843 m1A Human chr15 - 63048157 63048157 63048157 GTGGTGACCCGGGGTAACGGAGCTGGCTGCTAAGGGCAATAGCGACTCCTGCTGGCCGCGGGAGC GTGGTGACCCGGGGTAACGGAGCTGGCTGCTAGGGGCAATAGCGACTCCTGCTGGCCGCGGGAGC T C TPM1-AS Ensembl:ENSG00000259498 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63048153..63048302 26863196 MeRIP-seq:(Medium) rs1461563562 Functional Loss SNV dbSNP153 33..33 33 - - - 96452 RMVar_ID_96452 Human_SNP_ID_580360952 m1A Human chr15 + 63048328 63048328 63048328 TCCCCGCCGCCGCGAGCATGCGCAGTGCCCCCAGCCAGTCCCGGGATCCACGGCGCGCGCCCCTC TCCCCGCCGCCGCGAGCATGCGCAGTGCCCCCCGCCAGTCCCGGGATCCACGGCGCGCGCCCCTC A C TPM1 Ensembl:ENSG00000140416 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:63048325..63048423 32194978 MeRIP-seq:(Medium) rs1430944029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_172694 96453 RMVar_ID_96453 Human_SNP_ID_580361015 m1A Human chr15 + 63048420 63048420 63048420 GTCTGCGCAGCCCTGGAGGCTGCGACTTCCGGACTGCTCCTGGCCGCAGGGGGCGCCGCCATCGC GTCTGCGCAGCCCTGGAGGCTGCGACTTCCGGCCTGCTCCTGGCCGCAGGGGGCGCCGCCATCGC A C TPM1 Ensembl:ENSG00000140416 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:63048416..63048872 26863196 MeRIP-seq:(Medium) rs554540382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4327112 RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_172694 96454 RMVar_ID_96454 Human_SNP_ID_580361016 m1A Human chr15 + 63048420 63048420 63048420 GTCTGCGCAGCCCTGGAGGCTGCGACTTCCGGACTGCTCCTGGCCGCAGGGGGCGCCGCCATCGC GTCTGCGCAGCCCTGGAGGCTGCGACTTCCGGGCTGCTCCTGGCCGCAGGGGGCGCCGCCATCGC A G TPM1 Ensembl:ENSG00000140416 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:63048416..63048872 26863196 MeRIP-seq:(Medium) rs554540382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4327112 RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_172694 96455 RMVar_ID_96455 Human_SNP_ID_580361098 m1A Human chr15 + 63048519 63048519 63048519 GCAGCCAGGACAGCCGCGGCAGCCGGGTCCGCAGGGCAGCAGCCGGCCTCTCCCACTGCAGCCCT GCAGCCAGGACAGCCGCGGCAGCCGGGTCCGCTGGGCAGCAGCCGGCCTCTCCCACTGCAGCCCT A T TPM1 Ensembl:ENSG00000140416 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:63048516..63048872 32194978 MeRIP-seq:(Medium) rs920203347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342720 RMVar_hsa_circ_31981,RMVar_hsa_circ_85043,RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_350566,RMVar_hsa_circ_56303,RMVar_hsa_circ_95298,RMVar_hsa_circ_172694,RMVar_hsa_circ_172695 96456 RMVar_ID_96456 Human_SNP_ID_580361110 m1A Human chr15 - 63048535 63048535 63048535 ACGGTAGGCGGGCGGGAGGGCTGCAGTGGGAGAGGCCGGCTGCTGCCCTGCGGACCCGGCTGCCG ACGGTAGGCGGGCGGGAGGGCTGCAGTGGGAGGGGCCGGCTGCTGCCCTGCGGACCCGGCTGCCG T C TPM1-AS Ensembl:ENSG00000259498 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:63048501..63048650 26863196 MeRIP-seq:(Medium) rs1363224841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3201261 96457 RMVar_ID_96457 Human_SNP_ID_580363684 m1A Human chr15 - 63057092 63057092 63057092 TCTCACCTCTCACTCTCATCTGCTGCCTTCTCAGCTTCCTCCAGCTTCTGCAAAGCTGTTGCCAG TCTCACCTCTCACTCTCATCTGCTGCCTTCTCTGCTTCCTCCAGCTTCTGCAAAGCTGTTGCCAG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:63056906..63057125 26863196 MeRIP-seq:(Medium) rs1371734350 Functional Loss SNV dbSNP153 33..33 33 - - - 96458 RMVar_ID_96458 Human_SNP_ID_580363685 m1A Human chr15 - 63057092 63057092 63057092 TCTCACCTCTCACTCTCATCTGCTGCCTTCTCAGCTTCCTCCAGCTTCTGCAAAGCTGTTGCCAG TCTCACCTCTCACTCTCATCTGCTGCCTTCTCGGCTTCCTCCAGCTTCTGCAAAGCTGTTGCCAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:63056906..63057125 26863196 MeRIP-seq:(Medium) rs1371734350 Functional Loss SNV dbSNP153 33..33 33 - - - 96459 RMVar_ID_96459 Human_SNP_ID_580364258 m1A Human chr15 - 63059584 63059584 63059584 ATTTCCATTTTTTCTTCATCTTTTTGGGCTCGACTCTCAATGACTTTCATGCCTCTGAAAAGAAA ATTTCCATTTTTTCTTCATCTTTTTGGGCTCGGCTCTCAATGACTTTCATGCCTCTGAAAAGAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63056940..63059743 26863196 MeRIP-seq:(Medium) rs1197824702 Functional Loss SNV dbSNP153 33..33 33 - - - 96460 RMVar_ID_96460 Human_SNP_ID_580364985 m1A Human chr15 - 63062203 63062199 63062203 TCTGTCTTCCTTCTGCGAGTACTGTAATTAGAAAGAGCATTCCAGATGTCAGGCTGCAGCTCAAT TCTGTCTTCCTTCTGCGAGTACTGTAATTAGA____GCATTCCAGATGTCAGGCTGCAGCTCAAT CTCTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:63062201..63062300;chr15:63062201..63062250 26863196 MeRIP-seq:(Medium) rs1244768333 Functional Loss DEL dbSNP153 33..36 33 - - - 96461 RMVar_ID_96461 Human_SNP_ID_580381443 m1A Human chr15 + 63121884 63121884 63121884 GCCGGCTGTGCAGAGACGCCATGTACCGGCTCATGTCAGCAGTGACTGCCCGGGCTGCCGCCCCC GCCGGCTGTGCAGAGACGCCATGTACCGGCTCCTGTCAGCAGTGACTGCCCGGGCTGCCGCCCCC A C LACTB Ensembl:ENSG00000103642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63121850..63122123 26863196 MeRIP-seq:(Medium) rs34317102 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4342721,Human_RBP_ID_8804078,Human_RBP_ID_9283659 GWAS_ID_12660,GWAS_ID_12661,GWAS_ID_12662,GWAS_ID_12663,GWAS_ID_12664,GWAS_ID_12665,GWAS_ID_12666,GWAS_ID_12667,GWAS_ID_12668,GWAS_ID_12669,GWAS_ID_12670,GWAS_ID_12671,GWAS_ID_12672,GWAS_ID_12673,GWAS_ID_12674,GWAS_ID_12675,GWAS_ID_12676,GWAS_ID_12677,GWAS_ID_12678,GWAS_ID_12679,GWAS_ID_12680,GWAS_ID_12681,GWAS_ID_12682,GWAS_ID_12683,GWAS_ID_12684,GWAS_ID_12685,GWAS_ID_12686,GWAS_ID_12687,GWAS_ID_12688,GWAS_ID_12689,GWAS_ID_12690,GWAS_ID_12691,GWAS_ID_12692,GWAS_ID_12693,GWAS_ID_12694,GWAS_ID_12695,GWAS_ID_12696,GWAS_ID_12697,GWAS_ID_12698,GWAS_ID_12699,GWAS_ID_12700,GWAS_ID_12701,GWAS_ID_12702,GWAS_ID_12703,GWAS_ID_12704,GWAS_ID_12705,GWAS_ID_12706,GWAS_ID_12707,GWAS_ID_12708,GWAS_ID_12709,GWAS_ID_12710,GWAS_ID_12711,GWAS_ID_12712,GWAS_ID_12713,GWAS_ID_12714,GWAS_ID_12715,GWAS_ID_12716,GWAS_ID_12717,GWAS_ID_12718,GWAS_ID_12719 96462 RMVar_ID_96462 Human_SNP_ID_580381453 m1A Human chr15 + 63121896 63121896 63121896 GAGACGCCATGTACCGGCTCATGTCAGCAGTGACTGCCCGGGCTGCCGCCCCCGGGGGCTTGGCC GAGACGCCATGTACCGGCTCATGTCAGCAGTGGCTGCCCGGGCTGCCGCCCCCGGGGGCTTGGCC A G LACTB Ensembl:ENSG00000103642 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:63121851..63122104;chr15:63121854..63121960 26863196 MeRIP-seq:(Medium) rs1350934455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_460449,Human_RBP_ID_4327156,Human_RBP_ID_8804078,Human_RBP_ID_9283659 96463 RMVar_ID_96463 Human_SNP_ID_580398849 m1A Human chr15 - 63190375 63190375 63190375 CAAGTATCCTCATTCTGCCCTCTGATCCCTTGAACTCTTCTTCCACCTACAATTTTCTTCTGTCC CAAGTATCCTCATTCTGCCCTCTGATCCCTTGCACTCTTCTTCCACCTACAATTTTCTTCTGTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63189838..63190456 26863196 MeRIP-seq:(Medium) rs1261601835 Functional Loss SNV dbSNP153 33..33 33 - - - 96464 RMVar_ID_96464 Human_SNP_ID_580475999 m1A Human chr15 + 63504659 63504659 63504659 CGTCGGCCGAGCGCCCGGCTAGAAGCGACACCAGACGGAGCCTCCGGAGTTCCTCCGCCCCCACC CGTCGGCCGAGCGCCCGGCTAGAAGCGACACCGGACGGAGCCTCCGGAGTTCCTCCGCCCCCACC A G USP3 Ensembl:ENSG00000140455 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63504608..63504770 26863196 MeRIP-seq:(Medium) rs909141961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342728,Human_RBP_ID_18418375 96465 RMVar_ID_96465 Human_SNP_ID_580476000 m1A Human chr15 + 63504661 63504661 63504661 TCGGCCGAGCGCCCGGCTAGAAGCGACACCAGACGGAGCCTCCGGAGTTCCTCCGCCCCCACCTC TCGGCCGAGCGCCCGGCTAGAAGCGACACCAGGCGGAGCCTCCGGAGTTCCTCCGCCCCCACCTC A G USP3 Ensembl:ENSG00000140455 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:63504610..63504810;chr15:63504561..63504780 26863196 MeRIP-seq:(Medium) rs1203370332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342728,Human_RBP_ID_18418375 96466 RMVar_ID_96466 Human_SNP_ID_580476096 m1A Human chr15 + 63504858 63504858 63504858 CAGCGGTGAGTGCGGCCACGGGCCGGCCCCGCAGCGCACCCGAGGCCGCGGCTCTGCCGGGCCTG CAGCGGTGAGTGCGGCCACGGGCCGGCCCCGCCGCGCACCCGAGGCCGCGGCTCTGCCGGGCCTG A C USP3 Ensembl:ENSG00000140455 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:63504846..63504998;chr15:63504853..63505066 26863196 MeRIP-seq:(Medium) rs1402334149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19068319 96467 RMVar_ID_96467 Human_SNP_ID_580478000 m1A Human chr15 - 63512299 63512290 63512299 GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGAAGAAGAAGAGGAAGAAGAGGAAGAAGAAGAAGA GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGA_________GGAAGAAGAGGAAGAAGAAGAAGA CTCTTCTTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63512287..63512358 26863196 MeRIP-seq:(Medium) rs147194184 Functional Loss DEL dbSNP153 33..41 33 - - - 96468 RMVar_ID_96468 Human_SNP_ID_580478001 m1A Human chr15 - 63512299 63512290 63512299 GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGAAGAAGAAGAGGAAGAAGAGGAAGAAGAAGAAGA GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGA___AGAAGAGGAAGAAGAGGAAGAAGAAGAAGA CTCTTCTTCT CTCTTCT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63512287..63512358 26863196 MeRIP-seq:(Medium) rs147194184 Functional Loss DEL dbSNP153 33..35 33 - - - 96469 RMVar_ID_96469 Human_SNP_ID_580478010 m1A Human chr15 - 63512299 63512299 63512299 GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGAAGAAGAAGAGGAAGAAGAGGAAGAAGAAGAAGA GAGGAAGAAGAGGAAGAAGAAGAAGAGGAGGAGGAAGAAGAGGAAGAAGAGGAAGAAGAAGAAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63512287..63512358 26863196 MeRIP-seq:(Medium) rs1374210714 Functional Loss SNV dbSNP153 33..33 33 - - - 96470 RMVar_ID_96470 Human_SNP_ID_580486687 m1A Human chr15 + 63547851 63547851 63547851 AGAGAGAGAGAGAGAGAGGGAGGGAGGGAGAGAGAGAGAGAGAGGCATAGAGAGAGAGAGAGAGA AGAGAGAGAGAGAGAGAGGGAGGGAGGGAGAGGGAGAGAGAGAGGCATAGAGAGAGAGAGAGAGA A G USP3 Ensembl:ENSG00000140455 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63547806..63547909 26863196 MeRIP-seq:(Medium) rs981708872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25150939 RMVar_hsa_circ_57081,RMVar_hsa_circ_278294,RMVar_hsa_circ_287924,RMVar_hsa_circ_345614,RMVar_hsa_circ_106362,RMVar_hsa_circ_110130,RMVar_hsa_circ_97277,RMVar_hsa_circ_172737,RMVar_hsa_circ_172733,RMVar_hsa_circ_172726,RMVar_hsa_circ_172730,RMVar_hsa_circ_47752,RMVar_hsa_circ_53492,RMVar_hsa_circ_172731,RMVar_hsa_circ_172728,RMVar_hsa_circ_172729,RMVar_hsa_circ_172727,RMVar_hsa_circ_172725,RMVar_hsa_circ_124356,RMVar_hsa_circ_280939,RMVar_hsa_circ_302453,RMVar_hsa_circ_325000,RMVar_hsa_circ_343310,RMVar_hsa_circ_290781,RMVar_hsa_circ_271240,RMVar_hsa_circ_114761,RMVar_hsa_circ_172739,RMVar_hsa_circ_172740,RMVar_hsa_circ_172738,RMVar_hsa_circ_3654,RMVar_hsa_circ_172735,RMVar_hsa_circ_172736,RMVar_hsa_circ_172734,RMVar_hsa_circ_26489,RMVar_hsa_circ_297169,RMVar_hsa_circ_321384,RMVar_hsa_circ_323253,RMVar_hsa_circ_339194,RMVar_hsa_circ_311772,RMVar_hsa_circ_172744,RMVar_hsa_circ_172746,RMVar_hsa_circ_172747,RMVar_hsa_circ_172745,RMVar_hsa_circ_1674,RMVar_hsa_circ_341327,RMVar_hsa_circ_344120,RMVar_hsa_circ_354033,RMVar_hsa_circ_24016,RMVar_hsa_circ_172748 96471 RMVar_ID_96471 Human_SNP_ID_580520852 m1A Human chr15 + 63678034 63678034 63678034 GCCACACCTCTATGCAAAGAGTCCTCAGCTGCAGCTCTGAGAGGTCAGCGAGGCCATGCCTAGTA GCCACACCTCTATGCAAAGAGTCCTCAGCTGCCGCTCTGAGAGGTCAGCGAGGCCATGCCTAGTA A C AC073167.1 Ensembl:ENSG00000259589 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:63677985..63678141 26863196 MeRIP-seq:(Medium) rs1208083168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612411 96472 RMVar_ID_96472 Human_SNP_ID_580595056 m1A Human chr15 + 63970157 63970157 63970157 CCCAGCCAGAGGGATCACTCTGAAACAAGTACATGCTTACCTCACTTCTCTGCTCACCTGAACCC CCCAGCCAGAGGGATCACTCTGAAACAAGTACGTGCTTACCTCACTTCTCTGCTCACCTGAACCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63970155..63970283 26863196 MeRIP-seq:(Medium) rs1207744560 Functional Loss SNV dbSNP153 33..33 33 - - - 96473 RMVar_ID_96473 Human_SNP_ID_580595373 m1A Human chr15 + 63971557 63971556 63971557 CTGGGCCAGGAAATCGAAGAGCTCTCCTCCAGACACTCTGTAAAACACCAGCGGGGGGAGGGGAG CTGGGCCAGGAAATCGAAGAGCTCTCCTCCAG_CACTCTGTAAAACACCAGCGGGGGGAGGGGAG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63971531..63971596 26863196 MeRIP-seq:(Medium) rs778163387 Functional Loss DEL dbSNP153 33..33 33 - - - 96474 RMVar_ID_96474 Human_SNP_ID_580595375 m1A Human chr15 + 63971557 63971557 63971557 CTGGGCCAGGAAATCGAAGAGCTCTCCTCCAGACACTCTGTAAAACACCAGCGGGGGGAGGGGAG CTGGGCCAGGAAATCGAAGAGCTCTCCTCCAGTCACTCTGTAAAACACCAGCGGGGGGAGGGGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:63971531..63971596 26863196 MeRIP-seq:(Medium) rs200251366 Functional Loss SNV dbSNP153 33..33 33 - - - 96475 RMVar_ID_96475 Human_SNP_ID_580598300 m1A Human chr15 - 63983672 63983672 63983672 AGTATGCAGCCAAGTTCATCAAGAAGCGGCAGAGCCGGGCGAGCCGGCGCGGTGTGAGCCGGGAG AGTATGCAGCCAAGTTCATCAAGAAGCGGCAGGGCCGGGCGAGCCGGCGCGGTGTGAGCCGGGAG T C DAPK2 Ensembl:ENSG00000035664 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:63983628..63983703 26863196 MeRIP-seq:(Medium) rs1344771489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612416,Human_Splice_Rec_1612417,Human_Splice_Rec_1612436,Human_Splice_Rec_1612458,Human_Splice_Rec_1612496,Human_Splice_Rec_1612512,Human_Splice_Rec_1612532,Human_Splice_Rec_1612542,Human_Splice_Rec_1612543,Human_Splice_Rec_1612552,Human_Splice_Rec_1612560 RMVar_hsa_circ_48765,RMVar_hsa_circ_352321,RMVar_hsa_circ_352244,RMVar_hsa_circ_372516,RMVar_hsa_circ_172993 96476 RMVar_ID_96476 Human_SNP_ID_580598308 m1A Human chr15 - 63983680 63983680 63983680 GGGGCTTGAGTATGCAGCCAAGTTCATCAAGAAGCGGCAGAGCCGGGCGAGCCGGCGCGGTGTGA GGGGCTTGAGTATGCAGCCAAGTTCATCAAGAGGCGGCAGAGCCGGGCGAGCCGGCGCGGTGTGA T C DAPK2 Ensembl:ENSG00000035664 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:63983607..63983724 26863196 MeRIP-seq:(Medium) rs1233092511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612416,Human_Splice_Rec_1612417,Human_Splice_Rec_1612436,Human_Splice_Rec_1612458,Human_Splice_Rec_1612496,Human_Splice_Rec_1612512,Human_Splice_Rec_1612532,Human_Splice_Rec_1612542,Human_Splice_Rec_1612543,Human_Splice_Rec_1612552,Human_Splice_Rec_1612560 RMVar_hsa_circ_48765,RMVar_hsa_circ_352321,RMVar_hsa_circ_352244,RMVar_hsa_circ_372516,RMVar_hsa_circ_172993 96477 RMVar_ID_96477 Human_SNP_ID_580613628 m1A Human chr15 + 64046304 64046304 64046304 CGAGCCCGCAGACGGGTGCTACTCACGGCGGGAGGCTGAGCTGCCGCGGTCGCGGCCGCGGCAGG CGAGCCCGCAGACGGGTGCTACTCACGGCGGGGGGCTGAGCTGCCGCGGTCGCGGCCGCGGCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64046297..64046423 26863196 MeRIP-seq:(Medium) rs964494521 Functional Loss SNV dbSNP153 33..33 33 - - - 96478 RMVar_ID_96478 Human_SNP_ID_580625792 m1A Human chr15 + 64093720 64093720 64093720 GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCACAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCCCAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:64093670..64093770 32194978 MeRIP-seq:(Medium) rs748375266 Functional Loss SNV dbSNP153 33..33 33 - - - 96479 RMVar_ID_96479 Human_SNP_ID_580625793 m1A Human chr15 + 64093720 64093720 64093720 GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCACAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCGCAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:64093670..64093770 32194978 MeRIP-seq:(Medium) rs748375266 Functional Loss SNV dbSNP153 33..33 33 - - - 96480 RMVar_ID_96480 Human_SNP_ID_580625797 m1A Human chr15 - 64093727 64093727 64093727 GTGTCCGGGCTGCTCTCCTGGACGCTGAGCAGAGTCCTGTGGCTCTCCGGCCTCTCTGAGCCGGG GTGTCCGGGCTGCTCTCCTGGACGCTGAGCAGGGTCCTGTGGCTCTCCGGCCTCTCTGAGCCGGG T C CIAO2A Ensembl:ENSG00000166797 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64093676..64093875 26863196 MeRIP-seq:(Medium) rs1465389851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_460753,Human_RBP_ID_4327580,Human_RBP_ID_5316085,Human_RBP_ID_9324295,Human_RBP_ID_17651997,Human_RBP_ID_18189563,Human_RBP_ID_22440018,Human_RBP_ID_26327651 Human_Splice_Rec_1612569,Human_Splice_Rec_1612577,Human_Splice_Rec_1612583,Human_Splice_Rec_1612593,Human_Splice_Rec_1612597 RMVar_hsa_circ_111139,RMVar_hsa_circ_172997 96481 RMVar_ID_96481 Human_SNP_ID_580625811 m1A Human chr15 + 64093749 64093749 64093749 GCCACAGGACTCTGCTCAGCGTCCAGGAGAGCAGCCCGGACACCCGCTGCATCTTCACGCTCAGC GCCACAGGACTCTGCTCAGCGTCCAGGAGAGCCGCCCGGACACCCGCTGCATCTTCACGCTCAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64093701..64093875 26863196 MeRIP-seq:(Medium) rs1348967480 Functional Loss SNV dbSNP153 33..33 33 - - - 96482 RMVar_ID_96482 Human_SNP_ID_580625848 m1A Human chr15 + 64093801 64093801 64093801 CTTCACGCTCAGCCATCCCTGGCGACTGTCCCAATCGCGCCACCGTCTCTCAGCAGCCTCGGGAT CTTCACGCTCAGCCATCCCTGGCGACTGTCCCCATCGCGCCACCGTCTCTCAGCAGCCTCGGGAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64093651..64093850 26863196 MeRIP-seq:(Medium) rs1362165646 Functional Loss SNV dbSNP153 33..33 33 - - - 96483 RMVar_ID_96483 Human_SNP_ID_580626486 m1A Human chr15 - 64096043 64096043 64096043 AGGCCGGGGAAGGGCGGAGGCAGTCTCTCCGAAGCGCTACAGCCACCACCACCCGACGCCATCTT AGGCCGGGGAAGGGCGGAGGCAGTCTCTCCGAGGCGCTACAGCCACCACCACCCGACGCCATCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64095976..64096175;chr15:64095976..64112593 26863196 MeRIP-seq:(Medium) rs772549297 Functional Loss SNV dbSNP153 33..33 33 - - - 96484 RMVar_ID_96484 Human_SNP_ID_580626487 m1A Human chr15 - 64096043 64096043 64096043 AGGCCGGGGAAGGGCGGAGGCAGTCTCTCCGAAGCGCTACAGCCACCACCACCCGACGCCATCTT AGGCCGGGGAAGGGCGGAGGCAGTCTCTCCGACGCGCTACAGCCACCACCACCCGACGCCATCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64095976..64096175;chr15:64095976..64112593 26863196 MeRIP-seq:(Medium) rs772549297 Functional Loss SNV dbSNP153 33..33 33 - - - 96485 RMVar_ID_96485 Human_SNP_ID_580626493 m1A Human chr15 + 64096048 64096048 64096048 GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGAGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGCGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC A C SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64095976..64096222 26863196 MeRIP-seq:(Medium) rs140656810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759829,Human_RBP_ID_18418593,Human_RBP_ID_22934663,Human_RBP_ID_23659753,Human_RBP_ID_24544304 96486 RMVar_ID_96486 Human_SNP_ID_580626494 m1A Human chr15 + 64096048 64096048 64096048 GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGAGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGGGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC A G SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64095976..64096222 26863196 MeRIP-seq:(Medium) rs140656810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759829,Human_RBP_ID_18418593,Human_RBP_ID_22934663,Human_RBP_ID_23659753,Human_RBP_ID_24544304 96487 RMVar_ID_96487 Human_SNP_ID_580626495 m1A Human chr15 + 64096048 64096048 64096048 GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGAGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC GGCGTCGGGTGGTGGTGGCTGTAGCGCTTCGGTGAGACTGCCTCCGCCCTTCCCCGGCCTGGAGC A T SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64095976..64096222 26863196 MeRIP-seq:(Medium) rs140656810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759829,Human_RBP_ID_18418593,Human_RBP_ID_22934663,Human_RBP_ID_23659753,Human_RBP_ID_24544304 96488 RMVar_ID_96488 Human_SNP_ID_580626541 m1A Human chr15 - 64096121 64096121 64096121 AAAATGTCCTCCCCCTCGGTGTCGCTGTCCCCAGCCTCGGGTTCTGATCCCCCGGCCGCCCCCTC AAAATGTCCTCCCCCTCGGTGTCGCTGTCCCCTGCCTCGGGTTCTGATCCCCCGGCCGCCCCCTC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64096001..64096213 26863196 MeRIP-seq:(Medium) rs748632516 Functional Loss SNV dbSNP153 33..33 33 - - - 96489 RMVar_ID_96489 Human_SNP_ID_580626553 m1A Human chr15 + 64096155 64096155 64096155 GGGACAGCGACACCGAGGGGGAGGACATTTTCACCGGCGCCGCGGTGGTCGTGAGTTTGCACCCC GGGACAGCGACACCGAGGGGGAGGACATTTTCGCCGGCGCCGCGGTGGTCGTGAGTTTGCACCCC A G SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64096110..64096248 32194978 MeRIP-seq:(Medium) rs372800532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17863741,Human_RBP_ID_19068340,Human_RBP_ID_24544304 Human_Splice_Rec_1612637,Human_Splice_Rec_1612663,Human_Splice_Rec_1612689,Human_Splice_Rec_1612715,Human_Splice_Rec_1612729,Human_Splice_Rec_1612731,Human_Splice_Rec_1612753,Human_Splice_Rec_1612757 96490 RMVar_ID_96490 Human_SNP_ID_580638377 m1A Human chr15 + 64142443 64142443 64142443 TAAAGGTGGGACAAACTTAAGCATGTTAATAAAATTCAGAGAAGAGAAAGAGAATGACTATCAGA TAAAGGTGGGACAAACTTAAGCATGTTAATAACATTCAGAGAAGAGAAAGAGAATGACTATCAGA A C SNX1 Ensembl:ENSG00000028528 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64142393..64142551 26863196 MeRIP-seq:(Medium) rs1383607488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2449854,Human_RBP_ID_12550819 96491 RMVar_ID_96491 Human_SNP_ID_580642639 m1A Human chr15 - 64156819 64156817 64156819 GCCTGGCTGGGTGAGCATGGCCAACGCAGGCAAAGACACCAACGGCTCCCAGTTCTTCATCACGA GCCTGGCTGGGTGAGCATGGCCAACGCAGGCA__GACACCAACGGCTCCCAGTTCTTCATCACGA CTT C PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64156692..64156965 26863196 MeRIP-seq:(Medium) rs1211592084 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_42498,Human_RBP_ID_232282,Human_RBP_ID_460811,Human_RBP_ID_814806,Human_RBP_ID_1506270,Human_RBP_ID_1831634,Human_RBP_ID_4327742,Human_RBP_ID_12550875,Human_RBP_ID_22440024,Human_RBP_ID_22758846,Human_RBP_ID_22798958,Human_RBP_ID_27435952 Human_Splice_Rec_1612830,Human_Splice_Rec_1612831,Human_Splice_Rec_1612836 RMVar_hsa_circ_15445,RMVar_hsa_circ_173014,RMVar_hsa_circ_99698,RMVar_hsa_circ_103462,RMVar_hsa_circ_173015,RMVar_hsa_circ_320972 96492 RMVar_ID_96492 Human_SNP_ID_580642640 m1A Human chr15 - 64156819 64156819 64156819 GCCTGGCTGGGTGAGCATGGCCAACGCAGGCAAAGACACCAACGGCTCCCAGTTCTTCATCACGA GCCTGGCTGGGTGAGCATGGCCAACGCAGGCAGAGACACCAACGGCTCCCAGTTCTTCATCACGA T C PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64156692..64156965 26863196 MeRIP-seq:(Medium) rs773405777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42498,Human_RBP_ID_232282,Human_RBP_ID_460811,Human_RBP_ID_814806,Human_RBP_ID_1506270,Human_RBP_ID_1831634,Human_RBP_ID_4327742,Human_RBP_ID_12550875,Human_RBP_ID_22440024,Human_RBP_ID_22758846,Human_RBP_ID_22798958,Human_RBP_ID_27435952 Human_Splice_Rec_1612830,Human_Splice_Rec_1612831,Human_Splice_Rec_1612836 RMVar_hsa_circ_15445,RMVar_hsa_circ_173014,RMVar_hsa_circ_99698,RMVar_hsa_circ_103462,RMVar_hsa_circ_173015,RMVar_hsa_circ_320972 96493 RMVar_ID_96493 Human_SNP_ID_580643082 m1A Human chr15 - 64158575 64158575 64158575 GAGTAAGAGGATGACCCCTCACTTGGGGTGCCAGGGGAGTCATGTGGTGGCAGATCCAGGATGTG GAGTAAGAGGATGACCCCTCACTTGGGGTGCCCGGGGAGTCATGTGGTGGCAGATCCAGGATGTG T G PPIB Ensembl:ENSG00000166794 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64158571..64158691 26863196 MeRIP-seq:(Medium) rs1163618554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15445,RMVar_hsa_circ_103462,RMVar_hsa_circ_173015,RMVar_hsa_circ_320972 96494 RMVar_ID_96494 Human_SNP_ID_580643470 m1A Human chr15 - 64160154 64160153 64160154 CTACAAAAACAGCAAATTCCATCGTGTAATCAAGGACTTCATGATCCAGGGCGGAGACTTCACCA CTACAAAAACAGCAAATTCCATCGTGTAATCA_GGACTTCATGATCCAGGGCGGAGACTTCACCA CT C PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr15:64160044..64160242;chr15:64160039..64162175 26863196 MeRIP-seq:(Medium) rs1567346689 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_42500,Human_RBP_ID_460818,Human_RBP_ID_1506277,Human_RBP_ID_1831637,Human_RBP_ID_4327758,Human_RBP_ID_5180541,Human_RBP_ID_6446805,Human_RBP_ID_8801056,Human_RBP_ID_9054930,Human_RBP_ID_12550922,Human_RBP_ID_17483037,Human_RBP_ID_18665510,Human_RBP_ID_22758849,Human_RBP_ID_23659834,Human_RBP_ID_27435956,Human_RBP_ID_27559516 Human_Splice_Rec_1612828,Human_Splice_Rec_1612829,Human_Splice_Rec_1612834,Human_Splice_Rec_1612835,Human_Splice_Rec_1612840 RMVar_hsa_circ_15445,RMVar_hsa_circ_103462,RMVar_hsa_circ_173015,RMVar_hsa_circ_320972,RMVar_hsa_circ_266058 96495 RMVar_ID_96495 Human_SNP_ID_580643998 m1A Human chr15 - 64162092 64162092 64162092 GATGTAGGCCGGGTGATCTTTGGTCTCTTCGGAAAGACTGTTCCAAAAACAGTGGATAATTTTGT GATGTAGGCCGGGTGATCTTTGGTCTCTTCGGTAAGACTGTTCCAAAAACAGTGGATAATTTTGT T A PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64161996..64162191;chr15:64161975..64162175 26863196 MeRIP-seq:(Medium) rs370565028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43331,Human_RBP_ID_460823,Human_RBP_ID_759659,Human_RBP_ID_1506281,Human_RBP_ID_1831640,Human_RBP_ID_3478785,Human_RBP_ID_4327761,Human_RBP_ID_6446807,Human_RBP_ID_9054931,Human_RBP_ID_9371044,Human_RBP_ID_17870169,Human_RBP_ID_20090858,Human_RBP_ID_22439822,Human_RBP_ID_22758855,Human_RBP_ID_23659836,Human_RBP_ID_24544221,Human_RBP_ID_26932615,Human_RBP_ID_27232710 Human_Splice_Rec_1612826,Human_Splice_Rec_1612827,Human_Splice_Rec_1612838,Human_Splice_Rec_1612839 RMVar_hsa_circ_320972,RMVar_hsa_circ_266058 96496 RMVar_ID_96496 Human_SNP_ID_580643999 m1A Human chr15 - 64162092 64162092 64162092 GATGTAGGCCGGGTGATCTTTGGTCTCTTCGGAAAGACTGTTCCAAAAACAGTGGATAATTTTGT GATGTAGGCCGGGTGATCTTTGGTCTCTTCGGCAAGACTGTTCCAAAAACAGTGGATAATTTTGT T G PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64161996..64162191;chr15:64161975..64162175 26863196 MeRIP-seq:(Medium) rs370565028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43331,Human_RBP_ID_460823,Human_RBP_ID_759659,Human_RBP_ID_1506281,Human_RBP_ID_1831640,Human_RBP_ID_3478785,Human_RBP_ID_4327761,Human_RBP_ID_6446807,Human_RBP_ID_9054931,Human_RBP_ID_9371044,Human_RBP_ID_17870169,Human_RBP_ID_20090858,Human_RBP_ID_22439822,Human_RBP_ID_22758855,Human_RBP_ID_23659836,Human_RBP_ID_24544221,Human_RBP_ID_26932615,Human_RBP_ID_27232710 Human_Splice_Rec_1612826,Human_Splice_Rec_1612827,Human_Splice_Rec_1612838,Human_Splice_Rec_1612839 RMVar_hsa_circ_320972,RMVar_hsa_circ_266058 96497 RMVar_ID_96497 Human_SNP_ID_580644007 m1A Human chr15 + 64162120 64162120 64162120 TCTTTCCGAAGAGACCAAAGATCACCCGGCCTACATCTTCATCTCCAATTCGTAGGTCAAAATAC TCTTTCCGAAGAGACCAAAGATCACCCGGCCTGCATCTTCATCTCCAATTCGTAGGTCAAAATAC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64162101..64162125 26863196 MeRIP-seq:(Medium) rs758537632 Functional Loss SNV dbSNP153 33..33 33 - - - 96498 RMVar_ID_96498 Human_SNP_ID_580644300 m1A Human chr15 + 64162955 64162955 64162955 CGGACCCCGCGATGAGGGCGGCGGCAAGGAGCACCTTCATGTTGCGTTCGGAGAGGCGCAGCATC CGGACCCCGCGATGAGGGCGGCGGCAAGGAGCGCCTTCATGTTGCGTTCGGAGAGGCGCAGCATC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:64162861..64163067 26863196 MeRIP-seq:(Medium) rs759602757 Functional Loss SNV dbSNP153 33..33 33 - - - 96499 RMVar_ID_96499 Human_SNP_ID_580644304 m1A Human chr15 + 64162961 64162961 64162961 CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCATGTTGCGTTCGGAGAGGCGCAGCATCCACAGG CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCCTGTTGCGTTCGGAGAGGCGCAGCATCCACAGG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:64162910..64163058 32194978 MeRIP-seq:(Medium) rs137853864 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_564 GWAS_ID_12720 96500 RMVar_ID_96500 Human_SNP_ID_580644305 m1A Human chr15 + 64162961 64162961 64162961 CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCATGTTGCGTTCGGAGAGGCGCAGCATCCACAGG CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCGTGTTGCGTTCGGAGAGGCGCAGCATCCACAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:64162910..64163058 32194978 MeRIP-seq:(Medium) rs137853864 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_564 GWAS_ID_12720 96501 RMVar_ID_96501 Human_SNP_ID_580644306 m1A Human chr15 + 64162961 64162961 64162961 CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCATGTTGCGTTCGGAGAGGCGCAGCATCCACAGG CCGCGATGAGGGCGGCGGCAAGGAGCACCTTCTTGTTGCGTTCGGAGAGGCGCAGCATCCACAGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:64162910..64163058 32194978 MeRIP-seq:(Medium) rs137853864 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_564 GWAS_ID_12720 96502 RMVar_ID_96502 Human_SNP_ID_580644307 m1A Human chr15 - 64162962 64162962 64162962 GCCTGTGGATGCTGCGCCTCTCCGAACGCAACATGAAGGTGCTCCTTGCCGCCGCCCTCATCGCG GCCTGTGGATGCTGCGCCTCTCCGAACGCAACGTGAAGGTGCTCCTTGCCGCCGCCCTCATCGCG T C PPIB Ensembl:ENSG00000166794 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:64162811..64163125;chr15:64162816..64163149;chr15:64162802..64163148;chr15:64162799..64163156 26863196 MeRIP-seq:(Medium) rs1235014059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43333,Human_RBP_ID_1506284,Human_RBP_ID_3478786,Human_RBP_ID_4327766,Human_RBP_ID_8420126,Human_RBP_ID_18436597,Human_RBP_ID_18665512,Human_RBP_ID_22440031,Human_RBP_ID_26932618 GWAS_ID_12721 96503 RMVar_ID_96503 Human_SNP_ID_580644378 m1A Human chr15 + 64163055 64163055 64163055 GCCGGAAGAGGGTGGGGCCGCGGTGGCTAGGGAGCCGGCGCCGCCACGCGCGGGTGGGGGGGACT GCCGGAAGAGGGTGGGGCCGCGGTGGCTAGGGTGCCGGCGCCGCCACGCGCGGGTGGGGGGGACT A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:64162959..64163128 26863410 MeRIP-seq:(Medium) rs1055085892 Functional Loss SNV dbSNP153 33..33 33 - - - 96504 RMVar_ID_96504 Human_SNP_ID_580689202 m1A Human chr15 - 64343287 64343287 64343287 AATCCAGTCAAAGCAGTGTGTGCTAGGTGGGGAGGAAGGAGAAATAAGCCTACAGAGGCAGAATG AATCCAGTCAAAGCAGTGTGTGCTAGGTGGGGTGGAAGGAGAAATAAGCCTACAGAGGCAGAATG T A CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64343285..64343438 26863196 MeRIP-seq:(Medium) rs1341074997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12551960,Human_RBP_ID_23659947 96505 RMVar_ID_96505 Human_SNP_ID_580692465 m1A Human chr15 - 64356035 64356035 64356035 GGGTGGGTAGAGAAGCACTTGGCGCCTCGGGGAGGGGACCGCGCCCGCCTCATTTGCGCCTTGCA GGGTGGGTAGAGAAGCACTTGGCGCCTCGGGGGGGGGACCGCGCCCGCCTCATTTGCGCCTTGCA T C CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64355705..64356099 26863196 MeRIP-seq:(Medium) rs950790360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342734,Human_RBP_ID_18480917 Human_Splice_Rec_1612841,Human_Splice_Rec_1612863,Human_Splice_Rec_1612929,Human_Splice_Rec_1612953,Human_Splice_Rec_1613073 96506 RMVar_ID_96506 Human_SNP_ID_580692480 m1A Human chr15 - 64356082 64356082 64356082 CTTCTCCCCTCCCTCCCGCTCCTGGGAAAGAGAGAAACCACCGCTGCGGGTGGGTAGAGAAGCAC CTTCTCCCCTCCCTCCCGCTCCTGGGAAAGAGGGAAACCACCGCTGCGGGTGGGTAGAGAAGCAC T C CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64355970..64356127 26863196 MeRIP-seq:(Medium) rs974615276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342734 Human_Splice_Rec_1612841,Human_Splice_Rec_1612863,Human_Splice_Rec_1612929,Human_Splice_Rec_1612953,Human_Splice_Rec_1613073 96507 RMVar_ID_96507 Human_SNP_ID_580699296 m1A Human chr15 + 64381384 64381382 64381384 TCTGCTTTAGTCCGCACCATGTTCAAACAAGAAGAGAGGAGAGGAGAGAACGAACTGACTTCCCA TCTGCTTTAGTCCGCACCATGTTCAAACAAG__GAGAGGAGAGGAGAGAACGAACTGACTTCCCA GAA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64381234..64381450;chr15:64381229..64381450;chr15:64381282..64381510;chr15:64380975..64381461 26863196 MeRIP-seq:(Medium) rs1041801482 Functional Loss DEL dbSNP153 32..33 33 - - - 96508 RMVar_ID_96508 Human_SNP_ID_580699297 m1A Human chr15 + 64381384 64381384 64381384 TCTGCTTTAGTCCGCACCATGTTCAAACAAGAAGAGAGGAGAGGAGAGAACGAACTGACTTCCCA TCTGCTTTAGTCCGCACCATGTTCAAACAAGACGAGAGGAGAGGAGAGAACGAACTGACTTCCCA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64381234..64381450;chr15:64381229..64381450;chr15:64381282..64381510;chr15:64380975..64381461 26863196 MeRIP-seq:(Medium) rs928597808 Functional Loss SNV dbSNP153 33..33 33 - - - 96509 RMVar_ID_96509 Human_SNP_ID_580701123 m1A Human chr15 + 64387912 64387912 64387912 CGGTGTCCGGGGAGCCGCTGGTGCACTGGTGCACCCAGCAGTTGCGGAAGACTTTCGGCCTGGAT CGGTGTCCGGGGAGCCGCTGGTGCACTGGTGCGCCCAGCAGTTGCGGAAGACTTTCGGCCTGGAT A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64387861..64388020 26863196 MeRIP-seq:(Medium) rs768479725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342318,Human_RBP_ID_9371049,Human_RBP_ID_18982317 Human_Splice_Rec_1613301,Human_Splice_Rec_1613325,Human_Splice_Rec_1613337,Human_Splice_Rec_1613357 96510 RMVar_ID_96510 Human_SNP_ID_580702890 m1A Human chr15 + 64393996 64393996 64393996 GAGTGCTGAAGAGATACGAGAATATGTTACTGATCTCCTCCAGGGAAATGAAGGCAAAAAAGGTC GAGTGCTGAAGAGATACGAGAATATGTTACTGGTCTCCTCCAGGGAAATGAAGGCAAAAAAGGTC A G TRIP4 Ensembl:ENSG00000103671 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64393893..64393995 26863196 MeRIP-seq:(Medium) rs776939282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18665586,Human_RBP_ID_27809678 Human_Splice_Rec_1613280,Human_Splice_Rec_1613302,Human_Splice_Rec_1613338,Human_Splice_Rec_1613356,Human_Splice_Rec_1613358 RMVar_hsa_circ_64915,RMVar_hsa_circ_318822,RMVar_hsa_circ_354200,RMVar_hsa_circ_363524,RMVar_hsa_circ_331552,RMVar_hsa_circ_349512,RMVar_hsa_circ_329476,RMVar_hsa_circ_291720,RMVar_hsa_circ_318008,RMVar_hsa_circ_73798,RMVar_hsa_circ_173040,RMVar_hsa_circ_173042,RMVar_hsa_circ_173043,RMVar_hsa_circ_173041 96511 RMVar_ID_96511 Human_SNP_ID_580719984 m1A Human chr15 - 64461945 64461943 64461946 GATAAAATGACACGACTATTGTGTGTGGCAGCAGAACAGTCATCTCCTCACAACAGCCTAAACCA GATAAAATGACACGACTATTGTGTGTGGCAG___AACAGTCATCTCCTCACAACAGCCTAAACCA TCTG T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64461943..64462031 26863196 MeRIP-seq:(Medium) rs1165177369 Functional Loss DEL dbSNP153 32..34 33 - - - 96512 RMVar_ID_96512 Human_SNP_ID_580729913 m1A Human chr15 + 64499904 64499904 64499904 CAGTGTAGCCGGTTCCAAAAAGGAGAAGGAGAACAGCTCATCTAAGAGCAAGAAGGAGAGAAGCG CAGTGTAGCCGGTTCCAAAAAGGAGAAGGAGAGCAGCTCATCTAAGAGCAAGAAGGAGAGAAGCG A G ZNF609 Ensembl:ENSG00000180357 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64499832..64500106 26863196 MeRIP-seq:(Medium) rs370778220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12553506,Human_RBP_ID_25152583,Human_RBP_ID_27837554 RMVar_hsa_circ_93799,RMVar_hsa_circ_120107,RMVar_hsa_circ_173051,RMVar_hsa_circ_173052 96513 RMVar_ID_96513 Human_SNP_ID_580775055 m1A Human chr15 - 64674801 64674801 64674801 GCAATGGGACGGGCTGACTTTAGGCTCTTGGAAGGAATCTTTTCAGGTTTTAAACTAGAGGGTTT GCAATGGGACGGGCTGACTTTAGGCTCTTGGATGGAATCTTTTCAGGTTTTAAACTAGAGGGTTT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64674751..64674917 26863196 MeRIP-seq:(Medium) rs1243005877 Functional Loss SNV dbSNP153 33..33 33 - - - 96514 RMVar_ID_96514 Human_SNP_ID_580775077 m1A Human chr15 + 64674860 64674857 64674860 CATTGCCCCTGCCATCCCCCCACAGCAAATCTACACCTTCCAGACAGCCACCTTCACAGCAGCGA CATTGCCCCTGCCATCCCCCCACAGCAAAT___CACCTTCCAGACAGCCACCTTCACAGCAGCGA TCTA T ZNF609 Ensembl:ENSG00000180357 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64674810..64674960 26863196 MeRIP-seq:(Medium) rs1268398835 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17252415,Human_RBP_ID_27435994,Human_RBP_ID_27559523 RMVar_hsa_circ_1538,RMVar_hsa_circ_370522,RMVar_hsa_circ_173054,RMVar_hsa_circ_287111,RMVar_hsa_circ_348400,RMVar_hsa_circ_173057,RMVar_hsa_circ_112607,RMVar_hsa_circ_279396,RMVar_hsa_circ_347566,RMVar_hsa_circ_173058 96515 RMVar_ID_96515 Human_SNP_ID_580775078 m1A Human chr15 + 64674860 64674860 64674860 CATTGCCCCTGCCATCCCCCCACAGCAAATCTACACCTTCCAGACAGCCACCTTCACAGCAGCGA CATTGCCCCTGCCATCCCCCCACAGCAAATCTGCACCTTCCAGACAGCCACCTTCACAGCAGCGA A G ZNF609 Ensembl:ENSG00000180357 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64674810..64674960 26863196 MeRIP-seq:(Medium) rs1361173600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17252415,Human_RBP_ID_27435994,Human_RBP_ID_27559523 RMVar_hsa_circ_1538,RMVar_hsa_circ_370522,RMVar_hsa_circ_173054,RMVar_hsa_circ_287111,RMVar_hsa_circ_348400,RMVar_hsa_circ_173057,RMVar_hsa_circ_112607,RMVar_hsa_circ_279396,RMVar_hsa_circ_347566,RMVar_hsa_circ_173058 96516 RMVar_ID_96516 Human_SNP_ID_580775555 m1A Human chr15 - 64676188 64676188 64676188 TCGACCACACTCAGCACCTGTCTTGGCCTCAGAGGCCTCCTTGCTTAGGTGGCTGGCATCACTCA TCGACCACACTCAGCACCTGTCTTGGCCTCAGTGGCCTCCTTGCTTAGGTGGCTGGCATCACTCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64676138..64676239 32194978 MeRIP-seq:(Medium) rs1050706306 Functional Loss SNV dbSNP153 33..33 33 - - - 96517 RMVar_ID_96517 Human_SNP_ID_580776089 m1A Human chr15 + 64678237 64678237 64678237 CCGCAAATTGAAGGAGGAAAGGAGTCGGAGTAAGGACTCTGTCCCCAAGGAAGATGGGAAGGAAA CCGCAAATTGAAGGAGGAAAGGAGTCGGAGTAGGGACTCTGTCCCCAAGGAAGATGGGAAGGAAA A G ZNF609 Ensembl:ENSG00000180357 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64678188..64678400 26863196 MeRIP-seq:(Medium) rs149149419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26327664,Human_RBP_ID_27810447 RMVar_hsa_circ_1538,RMVar_hsa_circ_370522,RMVar_hsa_circ_173054,RMVar_hsa_circ_348400,RMVar_hsa_circ_27005,RMVar_hsa_circ_173057,RMVar_hsa_circ_112607,RMVar_hsa_circ_279396,RMVar_hsa_circ_173058 96518 RMVar_ID_96518 Human_SNP_ID_580776092 m1A Human chr15 - 64678246 64678246 64678246 TACTTGTGCTTTCCTTCCCATCTTCCTTGGGGACAGAGTCCTTACTCCGACTCCTTTCCTCCTTC TACTTGTGCTTTCCTTCCCATCTTCCTTGGGGTCAGAGTCCTTACTCCGACTCCTTTCCTCCTTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:64678198..64678385 26863196 MeRIP-seq:(Medium) rs757358403 Functional Loss SNV dbSNP153 33..33 33 - - - 96519 RMVar_ID_96519 Human_SNP_ID_580777144 m1A Human chr15 + 64682058 64682058 64682058 CCAAGCCCTTGGTCTGCTGCTGGAGCAGTACCAGCCCCCCCGCCCACCAGGGAGGGACCCCCACC CCAAGCCCTTGGTCTGCTGCTGGAGCAGTACCGGCCCCCCCGCCCACCAGGGAGGGACCCCCACC A G ZNF609 Ensembl:ENSG00000180357 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64682008..64682086 26863196 MeRIP-seq:(Medium) rs1354944575 Functional Loss SNV dbSNP153 33..33 33 - - - 96520 RMVar_ID_96520 Human_SNP_ID_580778579 m1A Human chr15 + 64687771 64687771 64687771 CCTAGGCCCTGCAGAGCAGAGTCTCAGACACTACTCGGAACCTGGTGGGGAGGCAGCTAGTACTA CCTAGGCCCTGCAGAGCAGAGTCTCAGACACTGCTCGGAACCTGGTGGGGAGGCAGCTAGTACTA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64687721..64687872 32194978 MeRIP-seq:(Medium) rs1163585439 Functional Loss SNV dbSNP153 33..33 33 - - - 96521 RMVar_ID_96521 Human_SNP_ID_580778767 m1A Human chr15 - 64688519 64688519 64688519 GTTGAAATTGTTTTCCATAAAGAACAGTATAAACATATTATTCACATGTAATCACCAATAGTAAA GTTGAAATTGTTTTCCATAAAGAACAGTATAAGCATATTATTCACATGTAATCACCAATAGTAAA T C OAZ2 Ensembl:ENSG00000180304 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64688468..64688719 32194978 MeRIP-seq:(Medium) rs942660779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1001391,Human_RBP_ID_1506365,Human_RBP_ID_1831758,Human_RBP_ID_6448126,Human_RBP_ID_8080752,Human_RBP_ID_17250576,Human_RBP_ID_17483110,Human_RBP_ID_17864025,Human_RBP_ID_26633156,Human_RBP_ID_27436019,Human_RBP_ID_27653162 RMVar_hsa_circ_173059,RMVar_hsa_circ_80160,RMVar_hsa_circ_121624,RMVar_hsa_circ_173060 96522 RMVar_ID_96522 Human_SNP_ID_580779635 m1A Human chr15 + 64691551 64691551 64691551 GCACCACAGAGGCCCTGGAACAATGTGCCTGCAGCACTGGAGCTGGGGACAGTTACTCAAAGGCA GCACCACAGAGGCCCTGGAACAATGTGCCTGCCGCACTGGAGCTGGGGACAGTTACTCAAAGGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64691501..64691644 26863196 MeRIP-seq:(Medium) rs907476653 Functional Loss SNV dbSNP153 33..33 33 - - - 96523 RMVar_ID_96523 Human_SNP_ID_580779636 m1A Human chr15 + 64691551 64691551 64691551 GCACCACAGAGGCCCTGGAACAATGTGCCTGCAGCACTGGAGCTGGGGACAGTTACTCAAAGGCA GCACCACAGAGGCCCTGGAACAATGTGCCTGCGGCACTGGAGCTGGGGACAGTTACTCAAAGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64691501..64691644 26863196 MeRIP-seq:(Medium) rs907476653 Functional Loss SNV dbSNP153 33..33 33 - - - 96524 RMVar_ID_96524 Human_SNP_ID_580781520 m1A Human chr15 - 64699098 64699098 64699098 GAGTCAAAGAGGAGAGAGAGAGAGACAGACACAGACTCTCCTAGTATAGTCAGGAATCCCCCAAA GAGTCAAAGAGGAGAGAGAGAGAGACAGACACGGACTCTCCTAGTATAGTCAGGAATCCCCCAAA T C OAZ2 Ensembl:ENSG00000180304 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64699096..64699167 26863196 MeRIP-seq:(Medium) rs374311280 Functional Loss SNV dbSNP153 33..33 33 - - - 96525 RMVar_ID_96525 Human_SNP_ID_580782618 m1A Human chr15 - 64703070 64703070 64703070 CCATCTATCCACTCCCTGCGCCGCCTCCTCCCACCCTGAGCAGAGCCGCCGAGGATGATAAACAC CCATCTATCCACTCCCTGCGCCGCCTCCTCCCCCCCTGAGCAGAGCCGCCGAGGATGATAAACAC T G OAZ2 Ensembl:ENSG00000180304 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64703026..64703200 26863196 MeRIP-seq:(Medium) rs554485978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4328153,Human_RBP_ID_5494520,Human_RBP_ID_26809482,Human_RBP_ID_27436030 Human_Splice_Rec_1613415,Human_Splice_Rec_1613429,Human_Splice_Rec_1613435,Human_Splice_Rec_1613441,Human_Splice_Rec_1613445,Human_Splice_Rec_1613451,Human_Splice_Rec_1613457 96526 RMVar_ID_96526 Human_SNP_ID_580782622 m1A Human chr15 + 64703077 64703077 64703077 TCATCCTCGGCGGCTCTGCTCAGGGTGGGAGGAGGCGGCGCAGGGAGTGGATAGATGGATGAGTG TCATCCTCGGCGGCTCTGCTCAGGGTGGGAGGCGGCGGCGCAGGGAGTGGATAGATGGATGAGTG A C AC100830.1 Ensembl:ENSG00000259635 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:64703026..64703200 26863196 MeRIP-seq:(Medium) rs759117983 Functional Loss SNV dbSNP153 33..33 33 - - - 96527 RMVar_ID_96527 Human_SNP_ID_580782659 m1A Human chr15 - 64703137 64703137 64703137 CGGCCTGACAGGGACTTAGCCCGCAGAGATCGACCCCGCGCGCGTGACCCCACACCCACCCACTC CGGCCTGACAGGGACTTAGCCCGCAGAGATCGTCCCCGCGCGCGTGACCCCACACCCACCCACTC T A OAZ2 Ensembl:ENSG00000180304 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:64703026..64703231 26863410 MeRIP-seq:(Medium) rs1180480285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342737 96528 RMVar_ID_96528 Human_SNP_ID_580795928 m1A Human chr15 + 64747313 64747313 64747313 GAGTCCCTGGAAGAACCTGAAAATGGACGTACACACAGCTCTCGGGCAGAGCACCCGACTCCTCC GAGTCCCTGGAAGAACCTGAAAATGGACGTACCCACAGCTCTCGGGCAGAGCACCCGACTCCTCC A C lnc-ZNF609-5 RNACentral:URS00008BFBDE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64747307..64747458 26863196 MeRIP-seq:(Medium) rs1348828703 Functional Loss SNV dbSNP153 33..33 33 - - - 96529 RMVar_ID_96529 Human_SNP_ID_580803279 m1A Human chr15 - 64772654 64772654 64772654 GTTAGACCTGTGGGGGTGGAAAAGGCATTCCAAGAGGAGGGAGTCGCATGTATAAGTGAGGAGGT GTTAGACCTGTGGGGGTGGAAAAGGCATTCCAGGAGGAGGGAGTCGCATGTATAAGTGAGGAGGT T C RBPMS2 Ensembl:ENSG00000166831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64772649..64772777 26863196 MeRIP-seq:(Medium) rs1349189441 Functional Loss SNV dbSNP153 33..33 33 - - - 96530 RMVar_ID_96530 Human_SNP_ID_580804176 m1A Human chr15 + 64775381 64775380 64775381 CGCGAGGGCGAGCGCGGCGCCGGCCCCGCGGGAAGTGGGAAGGGGCGCGGGGAGCGGTGCGCTCG CGCGAGGGCGAGCGCGGCGCCGGCCCCGCGGG_AGTGGGAAGGGGCGCGGGGAGCGGTGCGCTCG GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64775336..64775538 32194978 MeRIP-seq:(Medium) rs975261608 Functional Loss DEL dbSNP153 33..33 33 - - - 96531 RMVar_ID_96531 Human_SNP_ID_580804192 m1A Human chr15 + 64775423 64775412 64775423 GGGCGCGGGGAGCGGTGCGCTCGCGGGTGCGGAGCGGGTGGCGGGGGACCCACGGGGCAGTGAGA GGGCGCGGGGAGCGGTGCGCTC___________GCGGGTGGCGGGGGACCCACGGGGCAGTGAGA CGCGGGTGCGGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:64775326..64775625 26863410 MeRIP-seq:(Medium) rs1224692991 Functional Loss DEL dbSNP153 23..33 33 - - - 96532 RMVar_ID_96532 Human_SNP_ID_580804207 m1A Human chr15 - 64775471 64775471 64775471 GCACCCGCCAAACTTGATGTGACCCTGGCCCGACGCGGAGGCTGCCCCTCTCACTGCCCCGTGGG GCACCCGCCAAACTTGATGTGACCCTGGCCCGTCGCGGAGGCTGCCCCTCTCACTGCCCCGTGGG T A RBPMS2 Ensembl:ENSG00000166831 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64775182..64775559 26863196 MeRIP-seq:(Medium) rs1427752403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461024,Human_RBP_ID_4328187 96533 RMVar_ID_96533 Human_SNP_ID_580804398 m1A Human chr15 - 64775802 64775781 64775802 CCAGGCGAGAGAGAGGGGAAAGGCCCGGCCGGAGGCCGGCGCCCCGCGGCCGGGGCCGGGGCGAG CCAGGCGAGAGAGAGGGGAAAGGCCCGGCCGG_____________________GGCCGGGGCGAG CCCGGCCGCGGGGCGCCGGCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64775756..64775844 26863196 MeRIP-seq:(Medium) rs903286238 Functional Loss DEL dbSNP153 33..53 33 - - - 96534 RMVar_ID_96534 Human_SNP_ID_580816436 m1A Human chr15 - 64818199 64818199 64818199 CCTGCTACGGGGCTTTGCAGCATGGCCCCGGGAATGGTGGGGGGAGAAAAAGACTAGGAAGGAAA CCTGCTACGGGGCTTTGCAGCATGGCCCCGGGCATGGTGGGGGGAGAAAAAGACTAGGAAGGAAA T G PIF1 Ensembl:ENSG00000140451 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64818169..64818272 26863196 MeRIP-seq:(Medium) rs1335055045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355022 RMVar_hsa_circ_76459,RMVar_hsa_circ_101092,RMVar_hsa_circ_173064,RMVar_hsa_circ_291742,RMVar_hsa_circ_173065,RMVar_hsa_circ_173066 96535 RMVar_ID_96535 Human_SNP_ID_580817934 m1A Human chr15 - 64822910 64822890 64822910 TTGTGATAGGAAGAGAAACTTAGGTGACAGGAAGGAAACTTTAGTGACAGGATGAGAAGGGTTAG TTGTGATAGGAAGAGAAACTTAGGTGACAGGA____________________TGAGAAGGGTTAG ATCCTGTCACTAAAGTTTCCT A PIF1 Ensembl:ENSG00000140451 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64822860..64822999 26863196 MeRIP-seq:(Medium) rs1013506660 Functional Loss DEL dbSNP153 33..52 33 - - - Human_RBP_ID_2450351,Human_RBP_ID_6448227 RMVar_hsa_circ_101092,RMVar_hsa_circ_173065,RMVar_hsa_circ_345779,RMVar_hsa_circ_173071,RMVar_hsa_circ_113034,RMVar_hsa_circ_173074,RMVar_hsa_circ_173075,RMVar_hsa_circ_304375 96536 RMVar_ID_96536 Human_SNP_ID_580818187 m1A Human chr15 - 64823846 64823846 64823846 TGCAGCCCGAGGAGCGGCGGCTCAGGGCGGCCACCCGGGTTCCGGACACTACGCTGGTGAAGCGG TGCAGCCCGAGGAGCGGCGGCTCAGGGCGGCCCCCCGGGTTCCGGACACTACGCTGGTGAAGCGG T G PIF1 Ensembl:ENSG00000140451 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:64823798..64824001 26863196 MeRIP-seq:(Medium) rs755867842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1613497,Human_Splice_Rec_1613521,Human_Splice_Rec_1613545,Human_Splice_Rec_1613587 Human_miRNA_ID_2061635 RMVar_hsa_circ_101092,RMVar_hsa_circ_173065,RMVar_hsa_circ_345779,RMVar_hsa_circ_173071,RMVar_hsa_circ_113034,RMVar_hsa_circ_173074,RMVar_hsa_circ_173076,RMVar_hsa_circ_173075,RMVar_hsa_circ_304375,RMVar_hsa_circ_310571 96537 RMVar_ID_96537 Human_SNP_ID_580830156 m1A Human chr15 + 64867468 64867468 64867468 CAGCCTCCTTGTGCAAACTGGGCCCCCATGCCACAGTCTGGCTTTCCCTCCATCTGCCCCAGGAC CAGCCTCCTTGTGCAAACTGGGCCCCCATGCCTCAGTCTGGCTTTCCCTCCATCTGCCCCAGGAC A T AC069368.1,PLEKHO2 Ensembl:ENSG00000249240,Ensembl:ENSG00000241839 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64867261..64867808 32194978 MeRIP-seq:(Medium) rs902380385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5127815 RMVar_hsa_circ_81298,RMVar_hsa_circ_88570,RMVar_hsa_circ_37500,RMVar_hsa_circ_173077,RMVar_hsa_circ_173080 96538 RMVar_ID_96538 Human_SNP_ID_580852396 m1A Human chr15 + 64951657 64951651 64951658 TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTATCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT TCTTCTTTTCTTCTTCTATCTTCTTTC_______CTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT CCTTCTAT C ANKDD1A Ensembl:ENSG00000166839 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64951607..64951764 26863196 MeRIP-seq:(Medium) rs1158790030 Functional Loss DEL dbSNP153 28..34 33 - - - 96539 RMVar_ID_96539 Human_SNP_ID_580852400 m1A Human chr15 + 64951657 64951653 64951657 TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTATCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT TCTTCTTTTCTTCTTCTATCTTCTTTCCT____TCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT TTCTA T ANKDD1A Ensembl:ENSG00000166839 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64951607..64951764 26863196 MeRIP-seq:(Medium) rs1338951546 Functional Loss DEL dbSNP153 30..33 33 - - - 96540 RMVar_ID_96540 Human_SNP_ID_580852403 m1A Human chr15 + 64951657 64951657 64951657 TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTATCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTGTCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT A G ANKDD1A Ensembl:ENSG00000166839 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64951607..64951764 26863196 MeRIP-seq:(Medium) rs1193451683 Functional Loss SNV dbSNP153 33..33 33 - - - 96541 RMVar_ID_96541 Human_SNP_ID_580852404 m1A Human chr15 + 64951657 64951657 64951657 TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTATCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT TCTTCTTTTCTTCTTCTATCTTCTTTCCTTCTTTCTTCTTTTTCTTTCTTTCCTTCTTTCTTCTT A T ANKDD1A Ensembl:ENSG00000166839 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64951607..64951764 26863196 MeRIP-seq:(Medium) rs1193451683 Functional Loss SNV dbSNP153 33..33 33 - - - 96542 RMVar_ID_96542 Human_SNP_ID_580852980 m1A Human chr15 - 64952168 64952165 64952169 AGAAGAAGAAAAAGTAGAAGGAAAGAAGAAAGAAAAAGATGAAGAAAGAGGAAGAAGAATAAGGA AGAAGAAGAAAAAGTAGAAGGAAAGAAGAAA____AAGATGAAGAAAGAGGAAGAAGAATAAGGA TTTTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64951226..64955054 26863196 MeRIP-seq:(Medium) rs542562793 Functional Loss DEL dbSNP153 32..35 33 - - - 96543 RMVar_ID_96543 Human_SNP_ID_580852982 m1A Human chr15 - 64952168 64952167 64952169 AGAAGAAGAAAAAGTAGAAGGAAAGAAGAAAGAAAAAGATGAAGAAAGAGGAAGAAGAATAAGGA AGAAGAAGAAAAAGTAGAAGGAAAGAAGAAA__AAAAGATGAAGAAAGAGGAAGAAGAATAAGGA TTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64951226..64955054 26863196 MeRIP-seq:(Medium) rs1457254250 Functional Loss DEL dbSNP153 32..33 33 - - - 96544 RMVar_ID_96544 Human_SNP_ID_580853044 m1A Human chr15 - 64952273 64952236 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAA_________________________________ CTTCTTCTTATTCTTCTCCTTCTTCCTTCTCCTTCTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs1176552367 Functional Loss DEL dbSNP153 33..65 33 - - - 96545 RMVar_ID_96545 Human_SNP_ID_580853057 m1A Human chr15 - 64952258 64952251 64952258 AGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGAAGAAGAAAGGAGGAG AGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGA_______GAAGAATAAGAAGAAGAAAGGAGGAG CTCCTTCT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64952124..64952327 26863196 MeRIP-seq:(Medium) rs1176213234 Functional Loss DEL dbSNP153 33..39 33 - - - 96546 RMVar_ID_96546 Human_SNP_ID_580853064 m1A Human chr15 - 64952258 64952258 64952258 AGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGAAGAAGAAAGGAGGAG AGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAGGAAGGAGAAGAATAAGAAGAAGAAAGGAGGAG T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64952124..64952327 26863196 MeRIP-seq:(Medium) rs1199063677 Functional Loss SNV dbSNP153 33..33 33 - - - 96547 RMVar_ID_96547 Human_SNP_ID_580853066 m1A Human chr15 - 64952273 64952260 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAA_____________GAAGAAGGAGAAGAATAAGA CCTTCTCCTTCTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs971787629 Functional Loss DEL dbSNP153 33..45 33 - - - 96548 RMVar_ID_96548 Human_SNP_ID_580853067 m1A Human chr15 - 64952273 64952261 64952274 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGA_____________GGAAGAAGGAGAAGAATAAGA CTTCTCCTTCTTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs755148312 Functional Loss DEL dbSNP153 32..44 33 - - - 96549 RMVar_ID_96549 Human_SNP_ID_580853075 m1A Human chr15 - 64952271 64952267 64952271 GAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGAAG GAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAA____GGAGAAGGAAGAAGGAGAAGAATAAGAAG CTTCT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:64952212..64952388 26863196 MeRIP-seq:(Medium) rs372057618 Functional Loss DEL dbSNP153 33..36 33 - - - 96550 RMVar_ID_96550 Human_SNP_ID_580853078 m1A Human chr15 - 64952273 64952270 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAA___GAAGGAGAAGGAAGAAGGAGAAGAATAAGA CTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs907925508 Functional Loss DEL dbSNP153 33..35 33 - - - 96551 RMVar_ID_96551 Human_SNP_ID_580853079 m1A Human chr15 - 64952273 64952270 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAA__AGAAGGAGAAGGAAGAAGGAGAAGAATAAGA CTTT CT NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs907925508 Functional Loss DEL dbSNP153 33..34 33 - - - 96552 RMVar_ID_96552 Human_SNP_ID_580853080 m1A Human chr15 - 64952273 64952270 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAA_AAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA CTTT CTT NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs907925508 Functional Loss DEL dbSNP153 33..33 33 - - - 96553 RMVar_ID_96553 Human_SNP_ID_580853083 m1A Human chr15 - 64952273 64952273 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAATAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA T A NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs1169339764 Functional Loss SNV dbSNP153 33..33 33 - - - 96554 RMVar_ID_96554 Human_SNP_ID_580853084 m1A Human chr15 - 64952273 64952273 64952273 AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAAAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA AGGAGGAGGAGAGGAAGGAGAAGGAAGAAGAAGAAGAAGGAGAAGGAAGAAGGAGAAGAATAAGA T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64952173..64952300 26863196 MeRIP-seq:(Medium) rs1169339764 Functional Loss SNV dbSNP153 33..33 33 - - - 96555 RMVar_ID_96555 Human_SNP_ID_580853270 m1A Human chr15 - 64952473 64952458 64952474 AAGGAGAAGACGGTGACGAAGGAAGAAGAAGGAGAAGGAAGAAGGAGAAGAACTAAGAAGAAGAA AAGGAGAAGACGGTGACGAAGGAAGAAGAAG________________AAGAACTAAGAAGAAGAA TCTCCTTCTTCCTTCTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64951241..64955054;chr15:64951246..64955084 26863196 MeRIP-seq:(Medium) rs985838851 Functional Loss DEL dbSNP153 32..47 33 - - - 96556 RMVar_ID_96556 Human_SNP_ID_580853279 m1A Human chr15 - 64952473 64952469 64952473 AAGGAGAAGACGGTGACGAAGGAAGAAGAAGGAGAAGGAAGAAGGAGAAGAACTAAGAAGAAGAA AAGGAGAAGACGGTGACGAAGGAAGAAGAAGG____GGAAGAAGGAGAAGAACTAAGAAGAAGAA CTTCT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64951241..64955054;chr15:64951246..64955084 26863196 MeRIP-seq:(Medium) rs1566916675 Functional Loss DEL dbSNP153 33..36 33 - - - 96557 RMVar_ID_96557 Human_SNP_ID_580853280 m1A Human chr15 - 64952473 64952471 64952474 AAGGAGAAGACGGTGACGAAGGAAGAAGAAGGAGAAGGAAGAAGGAGAAGAACTAAGAAGAAGAA AAGGAGAAGACGGTGACGAAGGAAGAAGAAG___AAGGAAGAAGGAGAAGAACTAAGAAGAAGAA TCTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:64951241..64955054;chr15:64951246..64955084 26863196 MeRIP-seq:(Medium) rs1230094414 Functional Loss DEL dbSNP153 32..34 33 - - - 96558 RMVar_ID_96558 Human_SNP_ID_580853330 m1A Human chr15 - 64952535 64952521 64952536 AACGAAGGAGAAGGAAGGAGGAGGAGAAGGAGAAGAAGACGAAGGAAGAAGAAAGTAAGAAGAAG AACGAAGGAGAAGGAAGGAGGAGGAGAAGGA_______________AGAAGAAAGTAAGAAGAAG TTCCTTCGTCTTCTTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64952459..64952853 26863196 MeRIP-seq:(Medium) rs1394284095 Functional Loss DEL dbSNP153 32..46 33 - - - 96559 RMVar_ID_96559 Human_SNP_ID_580853347 m1A Human chr15 - 64952535 64952533 64952535 AACGAAGGAGAAGGAAGGAGGAGGAGAAGGAGAAGAAGACGAAGGAAGAAGAAAGTAAGAAGAAG AACGAAGGAGAAGGAAGGAGGAGGAGAAGGAG__GAAGACGAAGGAAGAAGAAAGTAAGAAGAAG CTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64952459..64952853 26863196 MeRIP-seq:(Medium) rs1237815823 Functional Loss DEL dbSNP153 33..34 33 - - - 96560 RMVar_ID_96560 Human_SNP_ID_580853497 m1A Human chr15 - 64952669 64952662 64952669 TAAGAAGAAAAAGGAGAGGAAGAAGAAGAAGGAAGAAGGGGAAGAAGAAGGAGAAGGAGAAGAAG TAAGAAGAAAAAGGAGAGGAAGAAGAAGAAGG_______GGAAGAAGAAGGAGAAGGAGAAGAAG CCCTTCTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:64952542..64952668 26863196 MeRIP-seq:(Medium) rs559007171 Functional Loss DEL dbSNP153 33..39 33 - - - 96561 RMVar_ID_96561 Human_SNP_ID_580854387 m1A Human chr15 - 64953547 64953534 64953547 GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAAGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGA_____________GGAGAAGAAGGAAGAAGGAG CTCTCCTTCTTCCT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64953498..64953599 26863196 MeRIP-seq:(Medium) rs1555397824 Functional Loss DEL dbSNP153 33..45 33 - - - 96562 RMVar_ID_96562 Human_SNP_ID_580854410 m1A Human chr15 - 64953547 64953542 64953548 GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAAGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG GAACTAAGAAGAAGGAGGAAGAAAGAAGGAG______GAAGGAGAGGAGAAGAAGGAAGAAGGAG CTTCCTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64953498..64953599 26863196 MeRIP-seq:(Medium) rs770686140 Functional Loss DEL dbSNP153 32..37 33 - - - 96563 RMVar_ID_96563 Human_SNP_ID_580854415 m1A Human chr15 - 64953547 64953547 64953547 GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAAGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAGGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64953498..64953599 26863196 MeRIP-seq:(Medium) rs1482170944 Functional Loss SNV dbSNP153 33..33 33 - - - 96564 RMVar_ID_96564 Human_SNP_ID_580854742 m1A Human chr15 - 64953743 64953738 64953744 AGGGAAGAGGAAGAAGAACGAAGAAAAGAGGAAAGAAGAAGGAGGAGAAGAAGGAGAAGAACAAG AGGGAAGAGGAAGAAGAACGAAGAAAAGAGG______GAAGGAGGAGAAGAAGGAGAAGAACAAG CTTCTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64953695..64953831 26863196 MeRIP-seq:(Medium) rs1171384044 Functional Loss DEL dbSNP153 32..37 33 - - - 96565 RMVar_ID_96565 Human_SNP_ID_580854747 m1A Human chr15 - 64953743 64953741 64953744 AGGGAAGAGGAAGAAGAACGAAGAAAAGAGGAAAGAAGAAGGAGGAGAAGAAGGAGAAGAACAAG AGGGAAGAGGAAGAAGAACGAAGAAAAGAGG___GAAGAAGGAGGAGAAGAAGGAGAAGAACAAG CTTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64953695..64953831 26863196 MeRIP-seq:(Medium) rs1189664897 Functional Loss DEL dbSNP153 32..34 33 - - - 96566 RMVar_ID_96566 Human_SNP_ID_580854749 m1A Human chr15 - 64953743 64953743 64953743 AGGGAAGAGGAAGAAGAACGAAGAAAAGAGGAAAGAAGAAGGAGGAGAAGAAGGAGAAGAACAAG AGGGAAGAGGAAGAAGAACGAAGAAAAGAGGAGAGAAGAAGGAGGAGAAGAAGGAGAAGAACAAG T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64953695..64953831 26863196 MeRIP-seq:(Medium) rs1469413725 Functional Loss SNV dbSNP153 33..33 33 - - - 96567 RMVar_ID_96567 Human_SNP_ID_580854824 m1A Human chr15 - 64953815 64953812 64953816 AGAAAAGAAGAGGAAAGAAGAAAAGAATAAGGAAGAAGAAAAAAAGGAAGAAGAAAGCAGAAGAA AGAAAAGAAGAGGAAAGAAGAAAAGAATAAG____AAGAAAAAAAGGAAGAAGAAAGCAGAAGAA TCTTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64953682..64953844 26863196 MeRIP-seq:(Medium) rs1410759764 Functional Loss DEL dbSNP153 32..35 33 - - - 96568 RMVar_ID_96568 Human_SNP_ID_580855651 m1A Human chr15 - 64954492 64954406 64954493 GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAGGAGAAGGAAGAAGAAAAAGAGGAAGAAGGAGAAG GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAG__________________________________ TCTTCTTCCTCCTCTCCTCCTTCGTTCGTCGTCTTCTCCTTCTTCTTCTTCCCTCTTCTCCTTCTTCCTCTTTTTCTTCTTCCTTCTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64954442..64954722 26863196 MeRIP-seq:(Medium) rs1566918762 Functional Loss DEL dbSNP153 32..65 33 - - - 96569 RMVar_ID_96569 Human_SNP_ID_580855726 m1A Human chr15 - 64954492 64954490 64954493 GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAGGAGAAGGAAGAAGAAAAAGAGGAAGAAGGAGAAG GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAG___AAGGAAGAAGAAAAAGAGGAAGAAGGAGAAG TCTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64954442..64954722 26863196 MeRIP-seq:(Medium) rs1195850212 Functional Loss DEL dbSNP153 32..34 33 - - - 96570 RMVar_ID_96570 Human_SNP_ID_580855729 m1A Human chr15 - 64954492 64954492 64954492 GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAGGAGAAGGAAGAAGAAAAAGAGGAAGAAGGAGAAG GAGAAGAAAGAGGAGAAGAAGGAAGAAGAAGGGGAAGGAAGAAGAAAAAGAGGAAGAAGGAGAAG T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64954442..64954722 26863196 MeRIP-seq:(Medium) rs1245773995 Functional Loss SNV dbSNP153 33..33 33 - - - 96571 RMVar_ID_96571 Human_SNP_ID_580855845 m1A Human chr15 - 64954635 64954621 64954636 AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAAGAAAAGGAAGAAGAAAAGAGGAAGGAGGAGGAAG AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAA_______________AAGAGGAAGGAGGAGGAAG TTTCTTCTTCCTTTTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64954516..64954696 26863196 MeRIP-seq:(Medium) rs1277313001 Functional Loss DEL dbSNP153 32..46 33 - - - 96572 RMVar_ID_96572 Human_SNP_ID_580855860 m1A Human chr15 - 64954635 64954633 64954636 AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAAGAAAAGGAAGAAGAAAAGAGGAAGGAGGAGGAAG AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAA___AAGGAAGAAGAAAAGAGGAAGGAGGAGGAAG TTTC T NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64954516..64954696 26863196 MeRIP-seq:(Medium) rs143099111 Functional Loss DEL dbSNP153 32..34 33 - - - 96573 RMVar_ID_96573 Human_SNP_ID_580855865 m1A Human chr15 - 64954635 64954635 64954635 AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAAGAAAAGGAAGAAGAAAAGAGGAAGGAGGAGGAAG AAGAAGAAAGAAGGAGAAGAAGAAGGAAGAAGTAAAGGAAGAAGAAAAGAGGAAGGAGGAGGAAG T A NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:64954516..64954696 26863196 MeRIP-seq:(Medium) rs12901916 Functional Loss SNV dbSNP153 33..33 33 - - - 96574 RMVar_ID_96574 Human_SNP_ID_580856072 m1A Human chr15 - 64954798 64954773 64954799 CAAAAAGAAGGAGAAGAACAAGGAAGAAGAACAACTAAGGAGAAGGAAGAAGGAGAAGAAGAAAG CAAAAAGAAGGAGAAGAACAAGGAAGAAGAA__________________________GAAGAAAG CTTCTCCTTCTTCCTTCTCCTTAGTTG C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:64954483..64954926 26863196 MeRIP-seq:(Medium) rs1566919208 Functional Loss DEL dbSNP153 32..57 33 - - - 96575 RMVar_ID_96575 Human_SNP_ID_580856285 m1A Human chr15 - 64954959 64954954 64954959 AGGAGAAGCAGGAGAAGAACAAGGAGAAGAAGAAGGAGAGAGAAGAAGAGACAAGAAGAAGGAGA AGGAGAAGCAGGAGAAGAACAAGGAGAAGAAG_____GAGAGAAGAAGAGACAAGAAGAAGGAGA CTCCTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64954908..64955013 26863196 MeRIP-seq:(Medium) rs1230559958 Functional Loss DEL dbSNP153 33..37 33 - - - 96576 RMVar_ID_96576 Human_SNP_ID_580856287 m1A Human chr15 - 64954959 64954956 64954959 AGGAGAAGCAGGAGAAGAACAAGGAGAAGAAGAAGGAGAGAGAAGAAGAGACAAGAAGAAGGAGA AGGAGAAGCAGGAGAAGAACAAGGAGAAGAAG___GAGAGAGAAGAAGAGACAAGAAGAAGGAGA CCTT C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64954908..64955013 26863196 MeRIP-seq:(Medium) rs757784134 Functional Loss DEL dbSNP153 33..35 33 - - - 96577 RMVar_ID_96577 Human_SNP_ID_580858527 m1A Human chr15 + 64963534 64963534 64963534 CACAGTGAGAACCGGTGAGCCTGACGAACCTGAAGGAAAAGGCTGGCTGACGGGTGCTGATGCCA CACAGTGAGAACCGGTGAGCCTGACGAACCTGCAGGAAAAGGCTGGCTGACGGGTGCTGATGCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64963484..64963615 26863196 MeRIP-seq:(Medium) rs1486098857 Functional Loss SNV dbSNP153 33..33 33 - - - 96578 RMVar_ID_96578 Human_SNP_ID_580861892 m1A Human chr15 + 64976529 64976529 64976529 AAAAGTTTTCTGAATCCATCACAGAACTCGAGATGGTCCCAATAAACTGGATACTGCAACTGAAA AAAAGTTTTCTGAATCCATCACAGAACTCGAGGTGGTCCCAATAAACTGGATACTGCAACTGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:64974722..64976547 32194978 MeRIP-seq:(Medium) rs139220894 Functional Loss SNV dbSNP153 33..33 33 - - - 96579 RMVar_ID_96579 Human_SNP_ID_580863080 m1A Human chr15 - 64981025 64981025 64981025 TTTCCACTTTTTTCTTTTAACCTTCCCTCCAGATTATTGTGGATGATGATGACAGTAAGATATGG TTTCCACTTTTTTCTTTTAACCTTCCCTCCAGGTTATTGTGGATGATGATGACAGTAAGATATGG T C SPG21 Ensembl:ENSG00000090487 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:64980954..64981055 26863410 MeRIP-seq:(Medium) rs146092558 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22650008 Human_Splice_Rec_1613786,Human_Splice_Rec_1613814,Human_Splice_Rec_1613830,Human_Splice_Rec_1613844,Human_Splice_Rec_1613860,Human_Splice_Rec_1613870,Human_Splice_Rec_1613876,Human_Splice_Rec_1613884,Human_Splice_Rec_1613890,Human_Splice_Rec_1613898,Human_Splice_Rec_1613904 RMVar_hsa_circ_173086,RMVar_hsa_circ_337636,RMVar_hsa_circ_300153,RMVar_hsa_circ_338386,RMVar_hsa_circ_290674,RMVar_hsa_circ_297923,RMVar_hsa_circ_273316,RMVar_hsa_circ_173087,RMVar_hsa_circ_173089,RMVar_hsa_circ_274069,RMVar_hsa_circ_309315,RMVar_hsa_circ_173090,RMVar_hsa_circ_173091,RMVar_hsa_circ_275558,RMVar_hsa_circ_309575,RMVar_hsa_circ_173092 96580 RMVar_ID_96580 Human_SNP_ID_580863747 m1A Human chr15 - 64983582 64983582 64983582 TATCACATGCTTTTATTTCAGGATTAACCTCCATTTCAGCTAATCATGGGAGAGATTAAAGTCTC TATCACATGCTTTTATTTCAGGATTAACCTCCTTTTCAGCTAATCATGGGAGAGATTAAAGTCTC T A SPG21 Ensembl:ENSG00000090487 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64983531..64987210 26863196 MeRIP-seq:(Medium) rs1345462948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884319,Human_RBP_ID_4342740,Human_RBP_ID_25153240 Human_Splice_Rec_1613784,Human_Splice_Rec_1613785,Human_Splice_Rec_1613812,Human_Splice_Rec_1613813,Human_Splice_Rec_1613828,Human_Splice_Rec_1613829,Human_Splice_Rec_1613842,Human_Splice_Rec_1613843,Human_Splice_Rec_1613858,Human_Splice_Rec_1613859,Human_Splice_Rec_1613868,Human_Splice_Rec_1613869,Human_Splice_Rec_1613882,Human_Splice_Rec_1613883,Human_Splice_Rec_1613888,Human_Splice_Rec_1613889,Human_Splice_Rec_1613896,Human_Splice_Rec_1613897,Human_Splice_Rec_1613902,Human_Splice_Rec_1613903,Human_Splice_Rec_1613906,Human_Splice_Rec_1613907 Human_miRNA_ID_2214626,Human_miRNA_ID_2214627 RMVar_hsa_circ_173086,RMVar_hsa_circ_337636,RMVar_hsa_circ_290674,RMVar_hsa_circ_273316,RMVar_hsa_circ_274069,RMVar_hsa_circ_173090,RMVar_hsa_circ_275558,RMVar_hsa_circ_173092 96581 RMVar_ID_96581 Human_SNP_ID_580865396 m1A Human chr15 - 64989758 64989758 64989758 CGTGGGTCCCGAGTGCTCCGCCGCCCGCCCCGACCCGGGCCCAGCCGCCTCCACGGCCCGCGCTC CGTGGGTCCCGAGTGCTCCGCCGCCCGCCCCGCCCCGGGCCCAGCCGCCTCCACGGCCCGCGCTC T G SPG21 Ensembl:ENSG00000090487 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:64989614..64989862 26863196 MeRIP-seq:(Medium) rs969054506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461104,Human_RBP_ID_4342321,Human_RBP_ID_5354498,Human_RBP_ID_18418380,Human_RBP_ID_22440032,Human_RBP_ID_26778922 Human_Splice_Rec_1613783,Human_Splice_Rec_1613827,Human_Splice_Rec_1613841,Human_Splice_Rec_1613855,Human_Splice_Rec_1613875,Human_Splice_Rec_1613905 96582 RMVar_ID_96582 Human_SNP_ID_580870472 m1A Human chr15 + 65010123 65010123 65010123 TTAGCTACTCTCCATCTTGCCAGCTATGCTCCAGCCACACCAGCCTCATTTCTGTCCCTCAAACA TTAGCTACTCTCCATCTTGCCAGCTATGCTCCCGCCACACCAGCCTCATTTCTGTCCCTCAAACA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:65009971..65010170 26863196 MeRIP-seq:(Medium) rs1161995703 Functional Loss SNV dbSNP153 33..33 33 - - - 96583 RMVar_ID_96583 Human_SNP_ID_580874678 m1A Human chr15 - 65026977 65026977 65026977 CTGGAGGTGGTCACAATGCCTTCCCCATCACCAAAAGGACTGCCAGTGAAGCAATATGCTGTGCA CTGGAGGTGGTCACAATGCCTTCCCCATCACCCAAAGGACTGCCAGTGAAGCAATATGCTGTGCA T G MTFMT Ensembl:ENSG00000103707 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:65026928..65027080 26863196 MeRIP-seq:(Medium) rs762875484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18981582 Human_Splice_Rec_1613912,Human_Splice_Rec_1613928,Human_Splice_Rec_1613946,Human_Splice_Rec_1613960,Human_Splice_Rec_1613966,Human_Splice_Rec_1613976 RMVar_hsa_circ_51546,RMVar_hsa_circ_36196,RMVar_hsa_circ_294548,RMVar_hsa_circ_173098,RMVar_hsa_circ_321451,RMVar_hsa_circ_338257 96584 RMVar_ID_96584 Human_SNP_ID_580899830 m1A Human chr15 + 65125163 65125163 65125163 CATGTGCATCACTACCTATCTTCATCTCCTTCATTTTCATGCTTGTGTAAGATGGGTCCTTCTTC CATGTGCATCACTACCTATCTTCATCTCCTTCCTTTTCATGCTTGTGTAAGATGGGTCCTTCTTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:65125160..65125301 26863196 MeRIP-seq:(Medium) rs1485397928 Functional Loss SNV dbSNP153 33..33 33 - - - 96585 RMVar_ID_96585 Human_SNP_ID_580901879 m1A Human chr15 - 65132962 65132962 65132962 AGGCCGCGCGGGCAGTGGAACGCGAGCAGGAGATTGACCGCTGGAGGGTGAAGTGTGTGCAGGAG AGGCCGCGCGGGCAGTGGAACGCGAGCAGGAGTTTGACCGCTGGAGGGTGAAGTGTGTGCAGGAG T A PDCD7 Ensembl:ENSG00000090470 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:65129076..65133125 26863196 MeRIP-seq:(Medium) rs1306358714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18665738,Human_RBP_ID_18982334 Human_Splice_Rec_1614031 96586 RMVar_ID_96586 Human_SNP_ID_580902235 m1A Human chr15 - 65133654 65133654 65133654 GCCCTCCCCGGCTTTCCCGCCGCCTCTCCCCCAGCGGCCCGGCCCTTTTCCGGGGGCCTCCGCCC GCCCTCCCCGGCTTTCCCGCCGCCTCTCCCCCCGCGGCCCGGCCCTTTTCCGGGGGCCTCCGCCC T G PDCD7 Ensembl:ENSG00000090470 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:65133592..65133769 26863196 MeRIP-seq:(Medium) rs764383900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461154,Human_RBP_ID_4328346,Human_RBP_ID_22532603,Human_RBP_ID_25153421 96587 RMVar_ID_96587 Human_SNP_ID_580902257 m1A Human chr15 + 65133710 65133710 65133710 GGGGAGGGCAGCGGCGGTGGCGGACAGCCGAAAGGAGCAGGAGGCGGCGGCTGCGGGGGCGGTGG GGGGAGGGCAGCGGCGGTGGCGGACAGCCGAAGGGAGCAGGAGGCGGCGGCTGCGGGGGCGGTGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:65133609..65133800 26863410 MeRIP-seq:(Medium) rs955221685 Functional Loss SNV dbSNP153 33..33 33 - - - 96588 RMVar_ID_96588 Human_SNP_ID_580915876 m1A Human chr15 + 65185191 65185191 65185191 CGAGGCCTAGGCCGGGGCTTCGCCCCCTGAGGACCTCCGGGTCACAGCGGCGTGAATCCTGCCCG CGAGGCCTAGGCCGGGGCTTCGCCCCCTGAGGGCCTCCGGGTCACAGCGGCGTGAATCCTGCCCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:65185146..65185320 26863196 MeRIP-seq:(Medium) rs763373829 Functional Loss SNV dbSNP153 33..33 33 - - - 96589 RMVar_ID_96589 Human_SNP_ID_580915891 m1A Human chr15 + 65185204 65185204 65185204 GGGGCTTCGCCCCCTGAGGACCTCCGGGTCACAGCGGCGTGAATCCTGCCCGCAAGGCGCGCTGA GGGGCTTCGCCCCCTGAGGACCTCCGGGTCACGGCGGCGTGAATCCTGCCCGCAAGGCGCGCTGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:65185158..65185350 26863196 MeRIP-seq:(Medium) rs1156856978 Functional Loss SNV dbSNP153 33..33 33 - - - 96590 RMVar_ID_96590 Human_SNP_ID_580915920 m1A Human chr15 + 65185298 65185298 65185298 GACCCCGTGGAGAGTTCACCTGCCCGGCAGCCAGGCCTTCACGCTTCTCTGCCCCACAGCCGTCT GACCCCGTGGAGAGTTCACCTGCCCGGCAGCCGGGCCTTCACGCTTCTCTGCCCCACAGCCGTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:65185121..65185350;chr15:65185120..65185350 26863196 MeRIP-seq:(Medium) rs905331762 Functional Loss SNV dbSNP153 33..33 33 - - - 96591 RMVar_ID_96591 Human_SNP_ID_580942180 m1A Human chr15 - 65286399 65286399 65286399 CTGGGATGCAGCCCTCAGGCTGGGCGGCCGCCAGGGAGGCGGCGGGCCGCGACATGCTGGCCGCC CTGGGATGCAGCCCTCAGGCTGGGCGGCCGCCGGGGAGGCGGCGGGCCGCGACATGCTGGCCGCC T C PARP16 Ensembl:ENSG00000138617 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:65286303..65286452 26863410 MeRIP-seq:(Medium) rs1329037585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461196,Human_RBP_ID_26809494 96592 RMVar_ID_96592 Human_SNP_ID_580942204 m1A Human chr15 - 65286437 65286437 65286437 CCCTAACCAGCGCGTCTACCCCGGCAACGCGCAGTGACCTGGGATGCAGCCCTCAGGCTGGGCGG CCCTAACCAGCGCGTCTACCCCGGCAACGCGCGGTGACCTGGGATGCAGCCCTCAGGCTGGGCGG T C PARP16 Ensembl:ENSG00000138617 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:65286348..65286653 26863196 MeRIP-seq:(Medium) rs943095573 Functional Loss SNV dbSNP153 33..33 33 - - - 96593 RMVar_ID_96593 Human_SNP_ID_580942205 m1A Human chr15 - 65286437 65286437 65286437 CCCTAACCAGCGCGTCTACCCCGGCAACGCGCAGTGACCTGGGATGCAGCCCTCAGGCTGGGCGG CCCTAACCAGCGCGTCTACCCCGGCAACGCGCCGTGACCTGGGATGCAGCCCTCAGGCTGGGCGG T G PARP16 Ensembl:ENSG00000138617 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:65286348..65286653 26863196 MeRIP-seq:(Medium) rs943095573 Functional Loss SNV dbSNP153 33..33 33 - - - 96594 RMVar_ID_96594 Human_SNP_ID_580975039 m1A Human chr15 - 65396405 65396405 65396405 CCGGGAGGAGCAATATTTAGGGGAGGCTGAGGAGGCCTGGGGACAGTTTTGGGAGAGAAAGAGAA CCGGGAGGAGCAATATTTAGGGGAGGCTGAGGGGGCCTGGGGACAGTTTTGGGAGAGAAAGAGAA T C IGDCC4 Ensembl:ENSG00000103742 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:65396359..65396449 26863196 MeRIP-seq:(Medium) rs1047364636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5157,RMVar_hsa_circ_173130,RMVar_hsa_circ_297608,RMVar_hsa_circ_173131,RMVar_hsa_circ_117347 96595 RMVar_ID_96595 Human_SNP_ID_580981959 m1A Human chr15 + 65423043 65423035 65423044 GCCGGCGCGGGGGCCAGGGCCGCTGCCGCCTCACCCGCCCCTCCATCGCCATCTTGGGCGAGCGG GCCGGCGCGGGGGCCAGGGCCGCTG_________CCGCCCCTCCATCGCCATCTTGGGCGAGCGG GCCGCCTCAC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:65422946..65423049 26863410 MeRIP-seq:(Medium) rs1404439322 Functional Loss DEL dbSNP153 26..34 33 - - - 96596 RMVar_ID_96596 Human_SNP_ID_580981963 m1A Human chr15 + 65423043 65423043 65423043 GCCGGCGCGGGGGCCAGGGCCGCTGCCGCCTCACCCGCCCCTCCATCGCCATCTTGGGCGAGCGG GCCGGCGCGGGGGCCAGGGCCGCTGCCGCCTCCCCCGCCCCTCCATCGCCATCTTGGGCGAGCGG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:65422946..65423049 26863410 MeRIP-seq:(Medium) rs970217284 Functional Loss SNV dbSNP153 33..33 33 - - - 96597 RMVar_ID_96597 Human_SNP_ID_580981964 m1A Human chr15 + 65423043 65423043 65423043 GCCGGCGCGGGGGCCAGGGCCGCTGCCGCCTCACCCGCCCCTCCATCGCCATCTTGGGCGAGCGG GCCGGCGCGGGGGCCAGGGCCGCTGCCGCCTCTCCCGCCCCTCCATCGCCATCTTGGGCGAGCGG A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:65422946..65423049 26863410 MeRIP-seq:(Medium) rs970217284 Functional Loss SNV dbSNP153 33..33 33 - - - 96598 RMVar_ID_96598 Human_SNP_ID_581007346 m1A Human chr15 + 65517635 65517635 65517635 CCGGTGACAACCCAGGCGGCGAACGCGGCACTAAGAAGCAGCGGCGGCAGTAGCAGCGGCCTTGG CCGGTGACAACCCAGGCGGCGAACGCGGCACTGAGAAGCAGCGGCGGCAGTAGCAGCGGCCTTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:65517429..65517662 26863196 MeRIP-seq:(Medium) rs917771284 Functional Loss SNV dbSNP153 33..33 33 - - - 96599 RMVar_ID_96599 Human_SNP_ID_581013535 m1A Human chr15 + 65540505 65540505 65540505 TGATATTCTAGCCGGGTGAAACTTGAAAGTTAAAACAAATGGTGCAGAAAGCTGGGGCAAGAACA TGATATTCTAGCCGGGTGAAACTTGAAAGTTACAACAAATGGTGCAGAAAGCTGGGGCAAGAACA A C HACD3 Ensembl:ENSG00000074696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:65540502..65540684 26863196 MeRIP-seq:(Medium) rs994265352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2450624,Human_RBP_ID_12557338 96600 RMVar_ID_96600 Human_SNP_ID_581022577 m1A Human chr15 + 65577199 65577199 65577199 GTAATCCCAGCACTTTGGGACACCTAGGTGGGAGCATCGCTTGAAGCCAGGAGTTCAAGACCAGC GTAATCCCAGCACTTTGGGACACCTAGGTGGGCGCATCGCTTGAAGCCAGGAGTTCAAGACCAGC A C HACD3 Ensembl:ENSG00000074696 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:65576902..65577203 32194978 MeRIP-seq:(Medium) rs570517381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461373,Human_RBP_ID_1237641,Human_RBP_ID_1831994,Human_RBP_ID_3479395,Human_RBP_ID_6449358,Human_RBP_ID_8801213,Human_RBP_ID_17250627,Human_RBP_ID_17365905,Human_RBP_ID_17483186,Human_RBP_ID_18281059,Human_RBP_ID_26438177,Human_RBP_ID_27653307 96601 RMVar_ID_96601 Human_SNP_ID_581022644 m1A Human chr15 + 65577426 65577422 65577427 AGCTGGGGTGACAGTGCAAGACCCTGTCTCAAACCAAACCAAACCACACACACACAAACACACAT AGCTGGGGTGACAGTGCAAGACCCTGTCT_____CAAACCAAACCACACACACACAAACACACAT TCAAAC T HACD3 Ensembl:ENSG00000074696 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:65577376..65577752 32194978 MeRIP-seq:(Medium) rs759666424 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_43009,Human_RBP_ID_461379,Human_RBP_ID_8251045,Human_RBP_ID_17250628,Human_RBP_ID_17365907,Human_RBP_ID_17483189,Human_RBP_ID_18512517,Human_RBP_ID_20004101,Human_RBP_ID_25154393,Human_RBP_ID_26435257 96602 RMVar_ID_96602 Human_SNP_ID_581030581 m1A Human chr15 + 65610896 65610896 65610896 GAGCAGAGGGCGAAATCGTGCAGTTTACGCGGAGCTGGGGACCCCGAGCCTCAGAGCGAGGGGAG GAGCAGAGGGCGAAATCGTGCAGTTTACGCGGTGCTGGGGACCCCGAGCCTCAGAGCGAGGGGAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:65610861..65611133 26863196 MeRIP-seq:(Medium) rs558641103 Functional Loss SNV dbSNP153 33..33 33 - - - 96603 RMVar_ID_96603 Human_SNP_ID_581030586 m1A Human chr15 + 65610910 65610910 65610910 ATCGTGCAGTTTACGCGGAGCTGGGGACCCCGAGCCTCAGAGCGAGGGGAGGCCGGGAGCAGCGC ATCGTGCAGTTTACGCGGAGCTGGGGACCCCGGGCCTCAGAGCGAGGGGAGGCCGGGAGCAGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:65610871..65611104 26863196 MeRIP-seq:(Medium) rs1566937129 Functional Loss SNV dbSNP153 33..33 33 - - - 96604 RMVar_ID_96604 Human_SNP_ID_581030666 m1A Human chr15 - 65611081 65611081 65611081 CGGCGATGGGCACGGGGTGAGTGGGGAGGCCGAGGGCCCGGGACTGCCTTTCGCTGCTTGTTGGG CGGCGATGGGCACGGGGTGAGTGGGGAGGCCGTGGGCCCGGGACTGCCTTTCGCTGCTTGTTGGG T A INTS14 Ensembl:ENSG00000138614 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:65610876..65611101 26863196 MeRIP-seq:(Medium) rs1283620076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759959,Human_RBP_ID_4342338,Human_RBP_ID_5355062 96605 RMVar_ID_96605 Human_SNP_ID_581039393 m1A Human chr15 + 65650641 65650641 65650641 AATGAAAGGTAATGAAGGTGAAACTGAAAGCCAGGAACTCAGTGCTGAAAATCACGGTGAAGCCA AATGAAAGGTAATGAAGGTGAAACTGAAAGCCGGGAACTCAGTGCTGAAAATCACGGTGAAGCCA A G SLC24A1 Ensembl:ENSG00000074621 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:65650458..65650874 26863196 MeRIP-seq:(Medium) rs1181634746 Functional Loss SNV dbSNP153 33..33 33 - - - 96606 RMVar_ID_96606 Human_SNP_ID_581041620 m1A Human chr15 - 65659696 65659696 65659696 TTGCACAGATTTAGTCTTAAAACCTAAAACACAAATACAAAGTGGTAAACCTGTTCAAAAGAAAA TTGCACAGATTTAGTCTTAAAACCTAAAACACTAATACAAAGTGGTAAACCTGTTCAAAAGAAAA T A DENND4A Ensembl:ENSG00000174485 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8031179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17000101 96607 RMVar_ID_96607 Human_SNP_ID_581041621 m1A Human chr15 - 65659696 65659696 65659696 TTGCACAGATTTAGTCTTAAAACCTAAAACACAAATACAAAGTGGTAAACCTGTTCAAAAGAAAA TTGCACAGATTTAGTCTTAAAACCTAAAACACGAATACAAAGTGGTAAACCTGTTCAAAAGAAAA T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8031179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17000101 96608 RMVar_ID_96608 Human_SNP_ID_581093448 m1A Human chr15 - 65869552 65869552 65869552 GCGCGGCCGAGGAGCGAAAGGGCGGGAGCAGCAGTGGTATCTGTGGGACCAGGGGGCGTCGCTGC GCGCGGCCGAGGAGCGAAAGGGCGGGAGCAGCCGTGGTATCTGTGGGACCAGGGGGCGTCGCTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:65869501..65870013 26863196 MeRIP-seq:(Medium) rs1265416382 Functional Loss SNV dbSNP153 33..33 33 - - - 96609 RMVar_ID_96609 Human_SNP_ID_581093461 m1A Human chr15 - 65869572 65869572 65869572 CGTCGTCGCGGGTGCCCATTGCGCGGCCGAGGAGCGAAAGGGCGGGAGCAGCAGTGGTATCTGTG CGTCGTCGCGGGTGCCCATTGCGCGGCCGAGGTGCGAAAGGGCGGGAGCAGCAGTGGTATCTGTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:65869476..65870013 26863196 MeRIP-seq:(Medium) rs1195767218 Functional Loss SNV dbSNP153 33..33 33 - - - 96610 RMVar_ID_96610 Human_SNP_ID_581095548 m1A Human chr15 - 65877327 65877327 65877327 CCAACACCAGAATCTCCAATAAGGACAACTGGAAAGACAAAGAATTCAATGTCAGATGAATGAGG CCAACACCAGAATCTCCAATAAGGACAACTGGGAAGACAAAGAATTCAATGTCAGATGAATGAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:65877326..65877350 26863196 MeRIP-seq:(Medium) rs1170747916 Functional Loss SNV dbSNP153 33..33 33 - - - 96611 RMVar_ID_96611 Human_SNP_ID_581096157 m1A Human chr15 + 65879750 65879750 65879750 AATGTAGAAGCTGCTTTTCAGACAATTTTAACAGGTAAGACTTGTATTTTCAGATTACACCAGTA AATGTAGAAGCTGCTTTTCAGACAATTTTAACGGGTAAGACTTGTATTTTCAGATTACACCAGTA A G RAB11A Ensembl:ENSG00000103769 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:65879726..65879775 32194978 MeRIP-seq:(Medium) rs1216536921 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_885690,Human_RBP_ID_17251993,Human_RBP_ID_22758872,Human_RBP_ID_27653395 Human_Splice_Rec_1615404,Human_Splice_Rec_1615405,Human_Splice_Rec_1615418,Human_Splice_Rec_1615419,Human_Splice_Rec_1615426,Human_Splice_Rec_1615427,Human_Splice_Rec_1615434,Human_Splice_Rec_1615442,Human_Splice_Rec_1615443 RMVar_hsa_circ_310464,RMVar_hsa_circ_173276,RMVar_hsa_circ_173278 96612 RMVar_ID_96612 Human_SNP_ID_581197895 m1A Human chr15 + 66293633 66293633 66293633 TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGACCTTCCAGGGCCGCACGCTGCGGATCGTGCGC TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGCCCTTCCAGGGCCGCACGCTGCGGATCGTGCGC A C DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66293584..66293680 26863196 MeRIP-seq:(Medium) rs902503635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 96613 RMVar_ID_96613 Human_SNP_ID_581197896 m1A Human chr15 + 66293633 66293633 66293633 TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGACCTTCCAGGGCCGCACGCTGCGGATCGTGCGC TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGGCCTTCCAGGGCCGCACGCTGCGGATCGTGCGC A G DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66293584..66293680 26863196 MeRIP-seq:(Medium) rs902503635 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 96614 RMVar_ID_96614 Human_SNP_ID_581197897 m1A Human chr15 + 66293633 66293633 66293633 TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGACCTTCCAGGGCCGCACGCTGCGGATCGTGCGC TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGTCCTTCCAGGGCCGCACGCTGCGGATCGTGCGC A T DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66293584..66293680 26863196 MeRIP-seq:(Medium) rs902503635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 96615 RMVar_ID_96615 Human_SNP_ID_581197911 m1A Human chr15 + 66293673 66293673 66293673 GGGCCGCACGCTGCGGATCGTGCGCGAGCACTACCTGCGGCCCTGCGTGCCCTGCCACAGCCCGC GGGCCGCACGCTGCGGATCGTGCGCGAGCACTGCCTGCGGCCCTGCGTGCCCTGCCACAGCCCGC A G DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66293624..66293689 26863196 MeRIP-seq:(Medium) rs1162761758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 Human_Splice_Rec_1615779,Human_Splice_Rec_1615801,Human_Splice_Rec_1615833,Human_Splice_Rec_1615855 96616 RMVar_ID_96616 Human_SNP_ID_581213483 m1A Human chr15 - 66356210 66356210 66356210 GTTCGATGTTTCAGGGATGGCACCCAAGGGGGACATCGAGGCAGCACGGTAGCACTTCCTTTGCG GTTCGATGTTTCAGGGATGGCACCCAAGGGGGTCATCGAGGCAGCACGGTAGCACTTCCTTTGCG T A TIPIN Ensembl:ENSG00000075131 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66356201..66356318 26863196 MeRIP-seq:(Medium) rs543851612 Functional Loss SNV dbSNP153 33..33 33 - - - 96617 RMVar_ID_96617 Human_SNP_ID_581221737 m1A Human chr15 - 66386968 66386968 66386968 GCACCAGAGCCCAGCTCCAGCTCCTGCCGGGGAAAGTGCCGCCGCCGCCGTGCTCCTAGCCGCTC GCACCAGAGCCCAGCTCCAGCTCCTGCCGGGGGAAGTGCCGCCGCCGCCGTGCTCCTAGCCGCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66386901..66387175 26863196 MeRIP-seq:(Medium) rs1022831120 Functional Loss SNV dbSNP153 33..33 33 - - - 96618 RMVar_ID_96618 Human_SNP_ID_581221742 m1A Human chr15 + 66386976 66386976 66386976 AGGAGCACGGCGGCGGCGGCACTTTCCCCGGCAGGAGCTGGAGCTGGGCTCTGGTGCGCGCGCGG AGGAGCACGGCGGCGGCGGCACTTTCCCCGGCGGGAGCTGGAGCTGGGCTCTGGTGCGCGCGCGG A G MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:66386926..66387125 26863196 MeRIP-seq:(Medium) rs1164167457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232300,Human_RBP_ID_4329401,Human_RBP_ID_5464123,Human_RBP_ID_8804093,Human_RBP_ID_8941196,Human_RBP_ID_9283687,Human_RBP_ID_18418488,Human_RBP_ID_22440047 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 96619 RMVar_ID_96619 Human_SNP_ID_581221759 m1A Human chr15 - 66387037 66387037 66387037 CCCGGGATTCCCTTCCTCTCTCTCTCTCAACCAACCAGTCCCTCCGGCTCGGGCGGCACAGCCGC CCCGGGATTCCCTTCCTCTCTCTCTCTCAACCTACCAGTCCCTCCGGCTCGGGCGGCACAGCCGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66386950..66387110 26863196 MeRIP-seq:(Medium) rs1327234154 Functional Loss SNV dbSNP153 33..33 33 - - - 96620 RMVar_ID_96620 Human_SNP_ID_581221785 m1A Human chr15 + 66387106 66387106 66387106 CGAACCGCACGTTCAGCCCGCTCCGCTCCTGCAGGGCAGCCTTTCGGCTCTCTGCGCGCGAAGCC CGAACCGCACGTTCAGCCCGCTCCGCTCCTGCGGGGCAGCCTTTCGGCTCTCTGCGCGCGAAGCC A G MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:66386986..66387150 26863196 MeRIP-seq:(Medium) rs1217046086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4937,Human_RBP_ID_4343202,Human_RBP_ID_5141276,Human_RBP_ID_5316092,Human_RBP_ID_5439772,Human_RBP_ID_8941196,Human_RBP_ID_9324300,Human_RBP_ID_9418462 Human_miRNA_ID_2381106,Human_miRNA_ID_3024121,Human_miRNA_ID_3090850 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 96621 RMVar_ID_96621 Human_SNP_ID_581221848 m1A Human chr15 + 66387279 66387260 66387279 CCGGACTTGGTCCTGCGCAGCGGGCGCGGGGCAGCGCAGCGGGAGGAAGCGAGAGGTGCTGCCCT CCGGACTTGGTCCT___________________GCGCAGCGGGAGGAAGCGAGAGGTGCTGCCCT TGCGCAGCGGGCGCGGGGCA T MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66387229..66387349 26863196 MeRIP-seq:(Medium) rs982392486 Functional Loss DEL dbSNP153 15..33 33 - - - Human_RBP_ID_4329415,Human_RBP_ID_21908570,Human_RBP_ID_22047543,Human_RBP_ID_22440355 Human_miRNA_ID_2151820,Human_miRNA_ID_2420287 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 96622 RMVar_ID_96622 Human_SNP_ID_581221856 m1A Human chr15 + 66387279 66387279 66387279 CCGGACTTGGTCCTGCGCAGCGGGCGCGGGGCAGCGCAGCGGGAGGAAGCGAGAGGTGCTGCCCT CCGGACTTGGTCCTGCGCAGCGGGCGCGGGGCGGCGCAGCGGGAGGAAGCGAGAGGTGCTGCCCT A G MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66387229..66387349 26863196 MeRIP-seq:(Medium) rs1053188266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4329415,Human_RBP_ID_21908570,Human_RBP_ID_22047543,Human_RBP_ID_22440355 Human_miRNA_ID_2151820,Human_miRNA_ID_2420287 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 96623 RMVar_ID_96623 Human_SNP_ID_581221866 m1A Human chr15 - 66387311 66387311 66387311 GACCCGGGTAACGCGCTTCCAACTCCGGGGGGAGGGCAGCACCTCTCGCTTCCTCCCGCTGCGCT GACCCGGGTAACGCGCTTCCAACTCCGGGGGGGGGGCAGCACCTCTCGCTTCCTCCCGCTGCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66387266..66387450 26863196 MeRIP-seq:(Medium) rs1352769336 Functional Loss SNV dbSNP153 33..33 33 - - - 96624 RMVar_ID_96624 Human_SNP_ID_581221873 m1A Human chr15 + 66387320 66387320 66387320 GGAGGAAGCGAGAGGTGCTGCCCTCCCCCCGGAGTTGGAAGCGCGTTACCCGGGTCCAAAATGCC GGAGGAAGCGAGAGGTGCTGCCCTCCCCCCGGTGTTGGAAGCGCGTTACCCGGGTCCAAAATGCC A T MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:66387176..66387350 26863410 MeRIP-seq:(Medium) rs1320811774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23661666 Human_miRNA_ID_2853264 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 96625 RMVar_ID_96625 Human_SNP_ID_581235000 m1A Human chr15 - 66435104 66435104 66435104 TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGAAAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGAGAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66435053..66435135 26863196 MeRIP-seq:(Medium) rs121908594 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_565 GWAS_ID_12722 96626 RMVar_ID_96626 Human_SNP_ID_581241452 m1A Human chr15 + 66460445 66460445 66460445 GTCAGGGAAAGGAATTCCAGGTAGAGGGAAGCATGAATCATGGCATAGAGGCAGGAAAACACAGA GTCAGGGAAAGGAATTCCAGGTAGAGGGAAGCGTGAATCATGGCATAGAGGCAGGAAAACACAGA A G MAP2K1 Ensembl:ENSG00000169032 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66460435..66460921 26863196 MeRIP-seq:(Medium) rs1336231851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_935,RMVar_hsa_circ_124504,RMVar_hsa_circ_126868,RMVar_hsa_circ_173294,RMVar_hsa_circ_173297,RMVar_hsa_circ_127706,RMVar_hsa_circ_173295,RMVar_hsa_circ_111063,RMVar_hsa_circ_173296,RMVar_hsa_circ_267335,RMVar_hsa_circ_112860,RMVar_hsa_circ_95846,RMVar_hsa_circ_173302,RMVar_hsa_circ_173303 96627 RMVar_ID_96627 Human_SNP_ID_581249977 m1A Human chr15 - 66493073 66493073 66493073 GTTATTTTGAGCTGCTTTTAGAGGAAACAGCCAGAAGTTTAAATGAGCATGTTCCTTAGAACACA GTTATTTTGAGCTGCTTTTAGAGGAAACAGCCGGAAGTTTAAATGAGCATGTTCCTTAGAACACA T C SNAPC5 Ensembl:ENSG00000174446 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12594835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1001562 GWAS_ID_12723,GWAS_ID_12724,GWAS_ID_12725,GWAS_ID_12726,GWAS_ID_12727,GWAS_ID_12728 96628 RMVar_ID_96628 Human_SNP_ID_581250375 m1A Human chr15 - 66494510 66494510 66494510 ATGTAGACAATGAAGCATCAATCAACCAAACAACCCTGGAGCTGAGCACAAAGAGTCATGTGACG ATGTAGACAATGAAGCATCAATCAACCAAACAGCCCTGGAGCTGAGCACAAAGAGTCATGTGACG T C SNAPC5 Ensembl:ENSG00000174446 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66494461..66494552 26863196 MeRIP-seq:(Medium) rs796052169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1506746,Human_RBP_ID_1832295,Human_RBP_ID_5464129,Human_RBP_ID_6451342,Human_RBP_ID_12562522,Human_RBP_ID_17250716,Human_RBP_ID_17365990,Human_RBP_ID_17864621,Human_RBP_ID_22934666,Human_RBP_ID_26326871,Human_RBP_ID_27436192,Human_RBP_ID_27810457 Human_Splice_Rec_1616024,Human_Splice_Rec_1616025,Human_Splice_Rec_1616030,Human_Splice_Rec_1616031,Human_Splice_Rec_1616036,Human_Splice_Rec_1616042,Human_Splice_Rec_1616046,Human_Splice_Rec_1616050,Human_Splice_Rec_1616052,Human_Splice_Rec_1616054 Human_miRNA_ID_726427 Clinvar_Rec_566 96629 RMVar_ID_96629 Human_SNP_ID_581251377 m1A Human chr15 + 66497730 66497730 66497730 CCTCCTTGCGCAGTTCCTGAAGCCGGCTCAGCATGTTGCCTGGTCACATAGCCAACCTCCGGGCT CCTCCTTGCGCAGTTCCTGAAGCCGGCTCAGCGTGTTGCCTGGTCACATAGCCAACCTCCGGGCT A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66497579..66497775 26863196 MeRIP-seq:(Medium) rs769573465 Functional Loss SNV dbSNP153 33..33 33 - - - 96630 RMVar_ID_96630 Human_SNP_ID_581252030 m1A Human chr15 - 66499447 66499447 66499447 CAAGAAACCAGCCCCTGAAAAGAAGCCTGCAGAGAAGAAACCTACTACAGAGGAGAAGAAGCCTG CAAGAAACCAGCCCCTGAAAAGAAGCCTGCAGCGAAGAAACCTACTACAGAGGAGAAGAAGCCTG T G RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66499406..66499495 26863196 MeRIP-seq:(Medium) rs1803776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461796,Human_RBP_ID_814808,Human_RBP_ID_886565,Human_RBP_ID_1506793,Human_RBP_ID_1832325,Human_RBP_ID_2451216,Human_RBP_ID_3479863,Human_RBP_ID_6451386,Human_RBP_ID_8251059,Human_RBP_ID_9055297,Human_RBP_ID_9371078,Human_RBP_ID_12562688,Human_RBP_ID_17483291,Human_RBP_ID_18436650,Human_RBP_ID_18528968,Human_RBP_ID_18666222,Human_RBP_ID_22930236,Human_RBP_ID_23661782,Human_RBP_ID_24544108,Human_RBP_ID_26326873,Human_RBP_ID_27809701 Human_miRNA_ID_3118368 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 96631 RMVar_ID_96631 Human_SNP_ID_581252108 m1A Human chr15 - 66499611 66499609 66499612 CGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACAAGCCAAATCAGATGAGAAGGCGGCGGT CGGGTGGATAAGGCAGCTGCTGCAGCAGCGG___TACAAGCCAAATCAGATGAGAAGGCGGCGGT AGTG A RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr15:66499557..66499647;chr15:66499411..66499799 26863196,32194978 MeRIP-seq:(Medium) rs764715249 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_42787,Human_RBP_ID_232351,Human_RBP_ID_461801,Human_RBP_ID_1001569,Human_RBP_ID_1506795,Human_RBP_ID_4346396,Human_RBP_ID_5178946,Human_RBP_ID_6451390,Human_RBP_ID_8801359,Human_RBP_ID_17250718,Human_RBP_ID_17365991,Human_RBP_ID_17483292,Human_RBP_ID_17864627,Human_RBP_ID_22192565,Human_RBP_ID_22496567,Human_RBP_ID_22930240,Human_RBP_ID_23661784,Human_RBP_ID_25186847,Human_RBP_ID_26435386,Human_RBP_ID_26933045,Human_RBP_ID_27233033,Human_RBP_ID_27653542 Human_Splice_Rec_1616072,Human_Splice_Rec_1616086,Human_Splice_Rec_1616088,Human_Splice_Rec_1616108,Human_Splice_Rec_1616124,Human_Splice_Rec_1616134 Human_miRNA_ID_2515870 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 96632 RMVar_ID_96632 Human_SNP_ID_581252113 m1A Human chr15 - 66499617 66499617 66499617 AAGCTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACAAGCCAAATCAGATGAGAAGGC AAGCTCCGGGTGGATAAGGCAGCTGCTGCAGCGGCGGCACTACAAGCCAAATCAGATGAGAAGGC T C RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:66499549..66499675;chr15:66499566..66499642;chr15:66499552..66499638 26863196 MeRIP-seq:(Medium) rs765207973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42787,Human_RBP_ID_232351,Human_RBP_ID_461801,Human_RBP_ID_759245,Human_RBP_ID_1001569,Human_RBP_ID_1506795,Human_RBP_ID_4346396,Human_RBP_ID_5178946,Human_RBP_ID_6451390,Human_RBP_ID_17250718,Human_RBP_ID_17365991,Human_RBP_ID_17483292,Human_RBP_ID_17864627,Human_RBP_ID_22192565,Human_RBP_ID_22496568,Human_RBP_ID_22930240,Human_RBP_ID_25186847,Human_RBP_ID_26435386,Human_RBP_ID_26933045,Human_RBP_ID_27233033 Human_Splice_Rec_1616072,Human_Splice_Rec_1616086,Human_Splice_Rec_1616088,Human_Splice_Rec_1616108,Human_Splice_Rec_1616124,Human_Splice_Rec_1616134 Human_miRNA_ID_2515870 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 96633 RMVar_ID_96633 Human_SNP_ID_581252115 m1A Human chr15 - 66499620 66499620 66499620 CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACAAGCCAAATCAGATGAGAA CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCTGCAGCGGCACTACAAGCCAAATCAGATGAGAA T A RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:66499376..66499675 26863196 MeRIP-seq:(Medium) rs773293158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42787,Human_RBP_ID_232351,Human_RBP_ID_461801,Human_RBP_ID_759245,Human_RBP_ID_886567,Human_RBP_ID_1506795,Human_RBP_ID_4346396,Human_RBP_ID_5178946,Human_RBP_ID_6451390,Human_RBP_ID_9371730,Human_RBP_ID_17252004,Human_RBP_ID_17366920,Human_RBP_ID_17484538,Human_RBP_ID_17864627,Human_RBP_ID_22192565,Human_RBP_ID_22496568,Human_RBP_ID_22930240,Human_RBP_ID_25186847,Human_RBP_ID_26435386,Human_RBP_ID_26933045,Human_RBP_ID_27233033 Human_Splice_Rec_1616072,Human_Splice_Rec_1616086,Human_Splice_Rec_1616088,Human_Splice_Rec_1616108,Human_Splice_Rec_1616124,Human_Splice_Rec_1616134 Human_miRNA_ID_2515870 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 96634 RMVar_ID_96634 Human_SNP_ID_581252116 m1A Human chr15 - 66499620 66499620 66499620 CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACAAGCCAAATCAGATGAGAA CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCGGCAGCGGCACTACAAGCCAAATCAGATGAGAA T C RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:66499376..66499675 26863196 MeRIP-seq:(Medium) rs773293158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42787,Human_RBP_ID_232351,Human_RBP_ID_461801,Human_RBP_ID_759245,Human_RBP_ID_886567,Human_RBP_ID_1506795,Human_RBP_ID_4346396,Human_RBP_ID_5178946,Human_RBP_ID_6451390,Human_RBP_ID_9371730,Human_RBP_ID_17252004,Human_RBP_ID_17366920,Human_RBP_ID_17484538,Human_RBP_ID_17864627,Human_RBP_ID_22192565,Human_RBP_ID_22496568,Human_RBP_ID_22930240,Human_RBP_ID_25186847,Human_RBP_ID_26435386,Human_RBP_ID_26933045,Human_RBP_ID_27233033 Human_Splice_Rec_1616072,Human_Splice_Rec_1616086,Human_Splice_Rec_1616088,Human_Splice_Rec_1616108,Human_Splice_Rec_1616124,Human_Splice_Rec_1616134 Human_miRNA_ID_2515870 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 96635 RMVar_ID_96635 Human_SNP_ID_581252352 m1A Human chr15 + 66500189 66500189 66500189 CTCTGCGATGGATCTTCTTGCTATAAAAAAGCAGATACTGTATCAACATTTTACTTAACATTATA CTCTGCGATGGATCTTCTTGCTATAAAAAAGCTGATACTGTATCAACATTTTACTTAACATTATA A T RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:66500187..66500304 26863196 MeRIP-seq:(Medium) rs1427843528 Functional Loss SNV dbSNP153 33..33 33 - - - 96636 RMVar_ID_96636 Human_SNP_ID_581252637 m1A Human chr15 - 66500991 66500991 66500991 TGAAAGTGCTTTCCGGAAGTTAGATGAATTGTACGGCACTTGGCGTAAAGCCGCTTCCCTCAAGA TGAAAGTGCTTTCCGGAAGTTAGATGAATTGTTCGGCACTTGGCGTAAAGCCGCTTCCCTCAAGA T A RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:66500926..66501056 32194978 MeRIP-seq:(Medium) rs756270719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42790,Human_RBP_ID_276960,Human_RBP_ID_298472,Human_RBP_ID_461806,Human_RBP_ID_886572,Human_RBP_ID_1001572,Human_RBP_ID_1175329,Human_RBP_ID_1506806,Human_RBP_ID_1832334,Human_RBP_ID_2451225,Human_RBP_ID_3479871,Human_RBP_ID_4346405,Human_RBP_ID_5178557,Human_RBP_ID_5566637,Human_RBP_ID_6451405,Human_RBP_ID_8251061,Human_RBP_ID_8420825,Human_RBP_ID_8801360,Human_RBP_ID_9055299,Human_RBP_ID_9283185,Human_RBP_ID_12562738,Human_RBP_ID_17250721,Human_RBP_ID_17365994,Human_RBP_ID_17483295,Human_RBP_ID_17689537,Human_RBP_ID_17864629,Human_RBP_ID_18281306,Human_RBP_ID_18666228,Human_RBP_ID_22046087,Human_RBP_ID_22496570,Human_RBP_ID_23661786,Human_RBP_ID_26435389,Human_RBP_ID_26933057,Human_RBP_ID_27233037,Human_RBP_ID_27436195,Human_RBP_ID_27653544 Human_Splice_Rec_1616067,Human_Splice_Rec_1616081,Human_Splice_Rec_1616103,Human_Splice_Rec_1616119,Human_Splice_Rec_1616141,Human_Splice_Rec_1616147 Human_miRNA_ID_2515871 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173308,RMVar_hsa_circ_113031,RMVar_hsa_circ_59010,RMVar_hsa_circ_92016,RMVar_hsa_circ_173312,RMVar_hsa_circ_116376,RMVar_hsa_circ_173313,RMVar_hsa_circ_173314 96637 RMVar_ID_96637 Human_SNP_ID_581252963 m1A Human chr15 - 66501793 66501793 66501793 TCCTTAAGAAACTTAAAGCCTGGAATGATATCAAAAAGGTCCGTTCAATGAGCACATTTACAGTT TCCTTAAGAAACTTAAAGCCTGGAATGATATCCAAAAGGTCCGTTCAATGAGCACATTTACAGTT T G RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:66501776..66501925 32194978 MeRIP-seq:(Medium) rs1194664576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886576,Human_RBP_ID_1506817,Human_RBP_ID_1832344,Human_RBP_ID_2451233,Human_RBP_ID_3479876,Human_RBP_ID_4329540,Human_RBP_ID_5523438,Human_RBP_ID_8420833,Human_RBP_ID_9055301,Human_RBP_ID_9371090,Human_RBP_ID_17483300,Human_RBP_ID_17864631,Human_RBP_ID_18281310,Human_RBP_ID_19068423,Human_RBP_ID_22046089,Human_RBP_ID_22192582,Human_RBP_ID_22799037,Human_RBP_ID_22935130,Human_RBP_ID_25156190,Human_RBP_ID_26933062,Human_RBP_ID_27233043,Human_RBP_ID_27653550 Human_Splice_Rec_1616063,Human_Splice_Rec_1616079,Human_Splice_Rec_1616099,Human_Splice_Rec_1616115,Human_Splice_Rec_1616137,Human_Splice_Rec_1616159,Human_Splice_Rec_1616184 Human_miRNA_ID_2068857 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_70834,RMVar_hsa_circ_173307,RMVar_hsa_circ_173308,RMVar_hsa_circ_113031,RMVar_hsa_circ_59010,RMVar_hsa_circ_92016,RMVar_hsa_circ_173312,RMVar_hsa_circ_116376,RMVar_hsa_circ_173313,RMVar_hsa_circ_173314,RMVar_hsa_circ_123696,RMVar_hsa_circ_173315,RMVar_hsa_circ_18223,RMVar_hsa_circ_119998,RMVar_hsa_circ_332385,RMVar_hsa_circ_173316 96638 RMVar_ID_96638 Human_SNP_ID_581253644 m1A Human chr15 + 66503510 66503510 66503510 CAGATGACTCCCCCTTTTCGGAGTACACCGATATCAGTGGGCGAGCACACGCCTAAAGAAAAAGA CAGATGACTCCCCCTTTTCGGAGTACACCGATGTCAGTGGGCGAGCACACGCCTAAAGAAAAAGA A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66503446..66503550 26863196 MeRIP-seq:(Medium) rs1214676901 Functional Loss SNV dbSNP153 33..33 33 - - - 96639 RMVar_ID_96639 Human_SNP_ID_581254074 m1A Human chr15 - 66504778 66504778 66504778 GGCTGTCTCCTCTCTCCGCCATGGTGAGTGGAAGTTCTCTTGGCTGGCCTTACCCCGTATCTCGG GGCTGTCTCCTCTCTCCGCCATGGTGAGTGGACGTTCTCTTGGCTGGCCTTACCCCGTATCTCGG T G RPL4 Ensembl:ENSG00000174444 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:66504776..66504825 26863196 MeRIP-seq:(Medium) rs1210583007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12562909,Human_RBP_ID_18418386,Human_RBP_ID_19067348 RMVar_hsa_circ_82571,RMVar_hsa_circ_173307,RMVar_hsa_circ_100348,RMVar_hsa_circ_173320 96640 RMVar_ID_96640 Human_SNP_ID_581305563 m1A Human chr15 + 66702301 66702296 66702301 CTCCTCCGGGGGCCCTCAGTGTGCGTTTGAGGAGAACAAAAAAGAGAGAGAGAGCCGAGCGGGGG CTCCTCCGGGGGCCCTCAGTGTGCGTTT_____GAACAAAAAAGAGAGAGAGAGCCGAGCGGGGG TGAGGA T SMAD6 Ensembl:ENSG00000137834 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr15:66702251..66702486;chr15:66702250..66702525 26863196 MeRIP-seq:(Medium) rs1567090423 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_5646261,Human_RBP_ID_18418387 96641 RMVar_ID_96641 Human_SNP_ID_581305593 m1A Human chr15 + 66702356 66702356 66702356 CGAGCGGGGGAGCGATCGAGGGAGCTGAGCCGAGAGAAAGAGCCGCCGGGCGCTGCCTCGCCAGA CGAGCGGGGGAGCGATCGAGGGAGCTGAGCCGGGAGAAAGAGCCGCCGGGCGCTGCCTCGCCAGA A G SMAD6 Ensembl:ENSG00000137834 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66702253..66702525 26863196 MeRIP-seq:(Medium) rs1462282390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4946,Human_RBP_ID_3488921,Human_RBP_ID_4329644,Human_RBP_ID_5646261,Human_RBP_ID_18161525,Human_RBP_ID_18418387 96642 RMVar_ID_96642 Human_SNP_ID_581305991 m1A Human chr15 - 66703298 66703298 66703298 TTCCTCCCGGTCGGGGACCACACGACTTCGCCAAAGTCGCCGCACCAGCCCCGAGCGTTTGGACC TTCCTCCCGGTCGGGGACCACACGACTTCGCCTAAGTCGCCGCACCAGCCCCGAGCGTTTGGACC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66703251..66703500 26863196 MeRIP-seq:(Medium) rs1353173742 Functional Loss SNV dbSNP153 33..33 33 - - - 96643 RMVar_ID_96643 Human_SNP_ID_581305992 m1A Human chr15 - 66703298 66703298 66703298 TTCCTCCCGGTCGGGGACCACACGACTTCGCCAAAGTCGCCGCACCAGCCCCGAGCGTTTGGACC TTCCTCCCGGTCGGGGACCACACGACTTCGCCGAAGTCGCCGCACCAGCCCCGAGCGTTTGGACC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66703251..66703500 26863196 MeRIP-seq:(Medium) rs1353173742 Functional Loss SNV dbSNP153 33..33 33 - - - 96644 RMVar_ID_96644 Human_SNP_ID_581306015 m1A Human chr15 + 66703337 66703331 66703337 GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GTCGTGTGGTCCCCGACCGGGAGGAAG______GCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GGCGGCA G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66703226..66703500 26863196 MeRIP-seq:(Medium) rs769605183 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_3489128,Human_RBP_ID_18481000,Human_RBP_ID_22192621,Human_RBP_ID_22712033 Clinvar_Rec_567 96645 RMVar_ID_96645 Human_SNP_ID_581306019 m1A Human chr15 + 66703337 66703334 66703337 GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GTCGTGTGGTCCCCGACCGGGAGGAAGGCG___GCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GGCA G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66703226..66703500 26863196 MeRIP-seq:(Medium) rs778673199 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_3489128,Human_RBP_ID_18481000,Human_RBP_ID_22192621,Human_RBP_ID_22712033 96646 RMVar_ID_96646 Human_SNP_ID_581306023 m1A Human chr15 + 66703337 66703337 66703337 GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCGGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66703226..66703500 26863196 MeRIP-seq:(Medium) rs374058045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489128,Human_RBP_ID_18481000,Human_RBP_ID_22192621,Human_RBP_ID_22712033 96647 RMVar_ID_96647 Human_SNP_ID_581306055 m1A Human chr15 + 66703362 66703362 66703362 AGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGAGGATGGGAGCTTGGGCAGCCGAGCTGAGCCGG AGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGGGGATGGGAGCTTGGGCAGCCGAGCTGAGCCGG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:66703276..66703600 26863196 MeRIP-seq:(Medium) rs770119498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489128,Human_RBP_ID_18481001,Human_RBP_ID_22712033 96648 RMVar_ID_96648 Human_SNP_ID_581306064 m1A Human chr15 + 66703370 66703370 66703370 GCGGCGGCGGCGGTGGCGGCGACGAGGATGGGAGCTTGGGCAGCCGAGCTGAGCCGGCCCCGCGG GCGGCGGCGGCGGTGGCGGCGACGAGGATGGGGGCTTGGGCAGCCGAGCTGAGCCGGCCCCGCGG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:66702974..66703821;chr15:66702783..66704123;chr15:66703101..66703792 26863196 MeRIP-seq:(Medium) rs1467107754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489128,Human_RBP_ID_18481001,Human_RBP_ID_22712033 96649 RMVar_ID_96649 Human_SNP_ID_581306340 m1A Human chr15 + 66703826 66703826 66703826 TGCTGAAGCGGCTCAAGGAGCGCTCGCTGGACACGCTGCTGGAGGCGGTGGAGTCCCGCGGCGGC TGCTGAAGCGGCTCAAGGAGCGCTCGCTGGACGCGCTGCTGGAGGCGGTGGAGTCCCGCGGCGGC A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:66703801..66703825 26863196 MeRIP-seq:(Medium) rs756623647 Functional Loss SNV dbSNP153 33..33 33 - - - 96650 RMVar_ID_96650 Human_SNP_ID_581306515 m1A Human chr15 + 66704043 66704043 66704043 CGCCGCCGCCGACGGCCCTACCGTGTGCTGCAACCCCTACCACTTCAGCCGGCTCTGCGGGCCCG CGCCGCCGCCGACGGCCCTACCGTGTGCTGCAGCCCCTACCACTTCAGCCGGCTCTGCGGGCCCG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66703993..66704219 26863196 MeRIP-seq:(Medium) rs1436851649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5464136,Human_RBP_ID_18436665,Human_RBP_ID_27436255 Human_Splice_Rec_1616511,Human_Splice_Rec_1616517 96651 RMVar_ID_96651 Human_SNP_ID_581306590 m1A Human chr15 - 66704128 66704128 66704128 CGACCCGCAGTGTCACAGAGAGAAGGGCACGGAAGGGGATGGGGACGGGGACCCGGGGCCCCCCC CGACCCGCAGTGTCACAGAGAGAAGGGCACGGTAGGGGATGGGGACGGGGACCCGGGGCCCCCCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:66703976..66704150 26863196 MeRIP-seq:(Medium) rs1235596970 Functional Loss SNV dbSNP153 33..33 33 - - - 96652 RMVar_ID_96652 Human_SNP_ID_581306642 m1A Human chr15 - 66704266 66704266 66704266 TAAGTTTACCGGAGCCTTGAGATAAAGTTGCCACTTGATGTGTGTGCTGGGACACCCACTCCCCT TAAGTTTACCGGAGCCTTGAGATAAAGTTGCCCCTTGATGTGTGTGCTGGGACACCCACTCCCCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66704101..66704275 26863196 MeRIP-seq:(Medium) rs1357086833 Functional Loss SNV dbSNP153 33..33 33 - - - 96653 RMVar_ID_96653 Human_SNP_ID_581307173 m1A Human chr15 + 66705940 66705938 66705940 GTCAGAGGAGAGGGAGCCAGCCGGGTCAGAGGAGAGGGAGCCAGCCAGCTCAGAGTCAAGGTGCC GTCAGAGGAGAGGGAGCCAGCCGGGTCAGAG__GAGGGAGCCAGCCAGCTCAGAGTCAAGGTGCC GGA G SMAD6 Ensembl:ENSG00000137834 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr15:66705744..66706150;chr15:66705776..66706100 26863196 MeRIP-seq:(Medium) rs1567092919 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6451600,Human_RBP_ID_12563281 96654 RMVar_ID_96654 Human_SNP_ID_581311218 m1A Human chr15 + 66720535 66720535 66720535 CTGACTCCATGCTGTGGGGCTGGAGGCGGCACACTGGGCAAGCTTCTTTAGGACCAGTAGCTCCC CTGACTCCATGCTGTGGGGCTGGAGGCGGCACGCTGGGCAAGCTTCTTTAGGACCAGTAGCTCCC A G SMAD6 Ensembl:ENSG00000137834 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:66720444..66720572 32194978 MeRIP-seq:(Medium) rs1334182831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96655 RMVar_ID_96655 Human_SNP_ID_581311973 m1A Human chr15 + 66723750 66723750 66723750 ATTATAAAAAGGGGGAAAAAAGAATCTACTACATGCCAGTGGCAGATGATAGAAAATGGAGAAAG ATTATAAAAAGGGGGAAAAAAGAATCTACTACGTGCCAGTGGCAGATGATAGAAAATGGAGAAAG A G SMAD6 Ensembl:ENSG00000137834 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66723746..66723995 26863196 MeRIP-seq:(Medium) rs12441023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96656 RMVar_ID_96656 Human_SNP_ID_581315598 m1A Human chr15 - 66738740 66738740 66738740 CCCATCAGAACCCGCTCTCTGGCCCCCGACACAGCCACTCCCACACCCACCCTGTCGCTTGGAGG CCCATCAGAACCCGCTCTCTGGCCCCCGACACGGCCACTCCCACACCCACCCTGTCGCTTGGAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:66738739..66738827 26863196 MeRIP-seq:(Medium) rs1435934487 Functional Loss SNV dbSNP153 33..33 33 - - - 96657 RMVar_ID_96657 Human_SNP_ID_581325945 m1A Human chr15 + 66781224 66781224 66781224 CGCGCAGCAAGATCGGCTTCGGCATCCTGCTCAGCAAGGAGCCCGACGGCGTGTGGGCCTACAAC CGCGCAGCAAGATCGGCTTCGGCATCCTGCTCGGCAAGGAGCCCGACGGCGTGTGGGCCTACAAC A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66781173..66781251 26863196 MeRIP-seq:(Medium) rs1235099986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461896,Human_RBP_ID_26809541 Human_miRNA_ID_2579847 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96658 RMVar_ID_96658 Human_SNP_ID_581325946 m1A Human chr15 + 66781224 66781224 66781224 CGCGCAGCAAGATCGGCTTCGGCATCCTGCTCAGCAAGGAGCCCGACGGCGTGTGGGCCTACAAC CGCGCAGCAAGATCGGCTTCGGCATCCTGCTCTGCAAGGAGCCCGACGGCGTGTGGGCCTACAAC A T SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66781173..66781251 26863196 MeRIP-seq:(Medium) rs1235099986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_461896,Human_RBP_ID_26809541 Human_miRNA_ID_2579847 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96659 RMVar_ID_96659 Human_SNP_ID_581325947 m1A Human chr15 + 66781228 66781228 66781228 CAGCAAGATCGGCTTCGGCATCCTGCTCAGCAAGGAGCCCGACGGCGTGTGGGCCTACAACCGCG CAGCAAGATCGGCTTCGGCATCCTGCTCAGCAGGGAGCCCGACGGCGTGTGGGCCTACAACCGCG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66781178..66781613 26863196 MeRIP-seq:(Medium) rs149949971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26809541 Human_miRNA_ID_2579847 Clinvar_Rec_568 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96660 RMVar_ID_96660 Human_SNP_ID_581326003 m1A Human chr15 + 66781297 66781297 66781297 GCACCCCATCTTCGTCAACTCCCCGACGCTGGACGCGCCCGGCGGCCGCGCCCTGGTCGTGCGCA GCACCCCATCTTCGTCAACTCCCCGACGCTGGCCGCGCCCGGCGGCCGCGCCCTGGTCGTGCGCA A C SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66781151..66781550 26863196 MeRIP-seq:(Medium) rs1288754635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18189577,Human_RBP_ID_26809037 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96661 RMVar_ID_96661 Human_SNP_ID_581326220 m1A Human chr15 + 66781582 66781582 66781582 GGAGGGGCGGGTGGGAGGCCGCGGCCACCGCCACCTGCCGGCCTCGAGAGGGGCCGATGCCCAGA GGAGGGGCGGGTGGGAGGCCGCGGCCACCGCCCCCTGCCGGCCTCGAGAGGGGCCGATGCCCAGA A C SMAD6 Ensembl:ENSG00000137834 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66781533..66781619 26863196 MeRIP-seq:(Medium) rs763746801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17366937,Human_RBP_ID_26327676 Human_miRNA_ID_2791004 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 96662 RMVar_ID_96662 Human_SNP_ID_581341165 m1A Human chr15 + 66842150 66842150 66842150 GACTGCCTCTCTGTCTTTTTATCTTTTTCACCAGGTCCTTCCTTCTCTTTTGCTCACTGCTGAAT GACTGCCTCTCTGTCTTTTTATCTTTTTCACCGGGTCCTTCCTTCTCTTTTGCTCACTGCTGAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66842104..66842169 26863196 MeRIP-seq:(Medium) rs1481869959 Functional Loss SNV dbSNP153 33..33 33 - - - 96663 RMVar_ID_96663 Human_SNP_ID_581341231 m1A Human chr15 + 66842412 66842412 66842412 GGCCTGTCCCACACCCTCTCTGCCGCCTGCCCAGTGACCTAATTATTGTTTTTTCTTCCAGCCCC GGCCTGTCCCACACCCTCTCTGCCGCCTGCCCGGTGACCTAATTATTGTTTTTTCTTCCAGCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66842363..66842574 26863196 MeRIP-seq:(Medium) rs555842966 Functional Loss SNV dbSNP153 33..33 33 - - - 96664 RMVar_ID_96664 Human_SNP_ID_581362350 m1A Human chr15 + 66928993 66928990 66928994 AAAGAAGAGAGAGAAAAAGAAAGAAAAGAGAGAAAGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA AAAGAAGAGAGAGAAAAAGAAAGAAAAGAG____AGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA GAGAA G AC093334.1 Ensembl:ENSG00000259437 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66928944..66929027 26863196 MeRIP-seq:(Medium) rs1354922319 Functional Loss DEL dbSNP153 31..34 33 - - - 96665 RMVar_ID_96665 Human_SNP_ID_581362353 m1A Human chr15 + 66928993 66928992 66928994 AAAGAAGAGAGAGAAAAAGAAAGAAAAGAGAGAAAGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA AAAGAAGAGAGAGAAAAAGAAAGAAAAGAGAG__AGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA GAA G AC093334.1 Ensembl:ENSG00000259437 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66928944..66929027 26863196 MeRIP-seq:(Medium) rs373019515 Functional Loss DEL dbSNP153 33..34 33 - - - 96666 RMVar_ID_96666 Human_SNP_ID_581362354 m1A Human chr15 + 66928993 66928993 66928993 AAAGAAGAGAGAGAAAAAGAAAGAAAAGAGAGAAAGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA AAAGAAGAGAGAGAAAAAGAAAGAAAAGAGAGCAAGAGAAAGAAAGAAGAGAGAAAGAGAAAGAA A C AC093334.1 Ensembl:ENSG00000259437 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:66928944..66929027 26863196 MeRIP-seq:(Medium) rs1228333817 Functional Loss SNV dbSNP153 33..33 33 - - - 96667 RMVar_ID_96667 Human_SNP_ID_581399198 m1A Human chr15 - 67077636 67077636 67077636 GATACCTCCAGAAATAGACCTGTTCTTCCTCTAGGCTCCCAAATATTTTGTTTGACCTTCACTAT GATACCTCCAGAAATAGACCTGTTCTTCCTCTCGGCTCCCAAATATTTTGTTTGACCTTCACTAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:67077629..67077839 26863196 MeRIP-seq:(Medium) rs915109293 Functional Loss SNV dbSNP153 33..33 33 - - - 96668 RMVar_ID_96668 Human_SNP_ID_581404587 m1A Human chr15 + 67098866 67098866 67098866 TCAGCTGGGGGATTTGGGGACGGTGGGAGGGCATACATGGATGGGAGGGTGGACTCCGTTCCTGA TCAGCTGGGGGATTTGGGGACGGTGGGAGGGCGTACATGGATGGGAGGGTGGACTCCGTTCCTGA A G SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:67098859..67098978 26863196 MeRIP-seq:(Medium) rs1427785912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489133,Human_RBP_ID_8182600,Human_RBP_ID_9418470,Human_RBP_ID_18481037,Human_RBP_ID_18937880,Human_RBP_ID_22696740,Human_RBP_ID_23273484 96669 RMVar_ID_96669 Human_SNP_ID_581409589 m1A Human chr15 + 67119066 67119066 67119066 GAGATATACATTTGTGAGTCATCATTGTATGGATGAGGCCGGGCTGGGGAGGATATGAGCGTAGA GAGATATACATTTGTGAGTCATCATTGTATGGGTGAGGCCGGGCTGGGGAGGATATGAGCGTAGA A G SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:67119063..67119219 26863196 MeRIP-seq:(Medium) rs1182824164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6451739,Human_RBP_ID_12564011 96670 RMVar_ID_96670 Human_SNP_ID_581415990 m1A Human chr15 + 67146425 67146425 67146425 GCCAGAGACCAGACTTTGAAGGTTATAGACCCAGGGCACGTGGCCAGAGCAGCTGTCAGTGGAGG GCCAGAGACCAGACTTTGAAGGTTATAGACCCGGGGCACGTGGCCAGAGCAGCTGTCAGTGGAGG A G SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:67146423..67146565 26863196 MeRIP-seq:(Medium) rs1184349234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6451761 RMVar_hsa_circ_173348,RMVar_hsa_circ_121746 96671 RMVar_ID_96671 Human_SNP_ID_581420534 m1A Human chr15 + 67164997 67164997 67164997 CGATGGCCAGACCTGCACAGCCACCACGAGCTACGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA CGATGGCCAGACCTGCACAGCCACCACGAGCTGCGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA A G SMAD3 Ensembl:ENSG00000166949 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1065080 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - Human_RBP_ID_18981608,Human_RBP_ID_26809038,Human_RBP_ID_27810465 Human_Splice_Rec_1616591,Human_Splice_Rec_1616597,Human_Splice_Rec_1616613,Human_Splice_Rec_1616621,Human_Splice_Rec_1616629,Human_Splice_Rec_1616645,Human_Splice_Rec_1616657,Human_Splice_Rec_1616673 Human_miRNA_ID_2450745,Human_miRNA_ID_2450746,Human_miRNA_ID_2540206,Human_miRNA_ID_2540207 Clinvar_Rec_569 GWAS_ID_12729,GWAS_ID_12730,GWAS_ID_12731,GWAS_ID_12732,GWAS_ID_12733,GWAS_ID_12734,GWAS_ID_12735 RMVar_hsa_circ_173349,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_270136,RMVar_hsa_circ_276738,RMVar_hsa_circ_43918,RMVar_hsa_circ_173350 96672 RMVar_ID_96672 Human_SNP_ID_581420535 m1A Human chr15 + 67164997 67164997 67164997 CGATGGCCAGACCTGCACAGCCACCACGAGCTACGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA CGATGGCCAGACCTGCACAGCCACCACGAGCTTCGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA A T SMAD3 Ensembl:ENSG00000166949 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1065080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18981608,Human_RBP_ID_26809038,Human_RBP_ID_27810465 Human_Splice_Rec_1616591,Human_Splice_Rec_1616597,Human_Splice_Rec_1616613,Human_Splice_Rec_1616621,Human_Splice_Rec_1616629,Human_Splice_Rec_1616645,Human_Splice_Rec_1616657,Human_Splice_Rec_1616673 Human_miRNA_ID_2450745,Human_miRNA_ID_2450746,Human_miRNA_ID_2540206,Human_miRNA_ID_2540207 Clinvar_Rec_569 GWAS_ID_12729,GWAS_ID_12730,GWAS_ID_12731,GWAS_ID_12732,GWAS_ID_12733,GWAS_ID_12734,GWAS_ID_12735 RMVar_hsa_circ_173349,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_270136,RMVar_hsa_circ_276738,RMVar_hsa_circ_43918,RMVar_hsa_circ_173350 96673 RMVar_ID_96673 Human_SNP_ID_581420682 m1A Human chr15 - 67165348 67165348 67165348 AATATTGCTCTGGGGCTCGATGCCTGCGGGGAAGTTAGTGTTTTCGGGGATGGAATGGCTGTAGT AATATTGCTCTGGGGCTCGATGCCTGCGGGGACGTTAGTGTTTTCGGGGATGGAATGGCTGTAGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:67165276..67165413 26863196 MeRIP-seq:(Medium) rs1566991832 Functional Loss SNV dbSNP153 33..33 33 - - - 96674 RMVar_ID_96674 Human_SNP_ID_581422700 m1A Human chr15 + 67173430 67173430 67173430 GTGCCATGTGTGAGCGGGCCCTTGAAGGACAGATGGGACCCTGTGAGGCAGAGAAGGATGGAAGG GTGCCATGTGTGAGCGGGCCCTTGAAGGACAGTTGGGACCCTGTGAGGCAGAGAAGGATGGAAGG A T SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:67173265..67173562 26863196 MeRIP-seq:(Medium) rs879782705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12564182 RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353 96675 RMVar_ID_96675 Human_SNP_ID_581422909 m1A Human chr15 + 67174338 67174338 67174338 GCTGAAGTCATGCCAGTGGATGGATTTAGTGGAGAGGCCGACCCAGCTCAAGATGGAAAGACAGC GCTGAAGTCATGCCAGTGGATGGATTTAGTGGGGAGGCCGACCCAGCTCAAGATGGAAAGACAGC A G SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:67174335..67174514 26863196 MeRIP-seq:(Medium) rs1448780389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8420945,Human_RBP_ID_12564192 RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353 96676 RMVar_ID_96676 Human_SNP_ID_581424400 m1A Human chr15 - 67180121 67180121 67180121 TGCACTGCACTGACTGCTGGGCGCGAGCCCTTAGCCTACGACACTCTGCTTGATGCCTACCTGAA TGCACTGCACTGACTGCTGGGCGCGAGCCCTTGGCCTACGACACTCTGCTTGATGCCTACCTGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:67180117..67180371 26863196 MeRIP-seq:(Medium) rs1470766026 Functional Loss SNV dbSNP153 33..33 33 - - - 96677 RMVar_ID_96677 Human_SNP_ID_581424702 m1A Human chr15 + 67181323 67181300 67181324 TACTACGAGCTGAACCAGCGCGTCGGGGAGACATTCCACGCCTCGCAGCCATCCATGACTGTGGA TACTACGAGC________________________TCCACGCCTCGCAGCCATCCATGACTGTGGA CTGAACCAGCGCGTCGGGGAGACAT C SMAD3 Ensembl:ENSG00000166949 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:67181251..67181350 26863196 MeRIP-seq:(Medium) rs1566999378 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_9371101 Human_Splice_Rec_1616604,Human_Splice_Rec_1616636,Human_Splice_Rec_1616652,Human_Splice_Rec_1616664,Human_Splice_Rec_1616680,Human_Splice_Rec_1616690,Human_Splice_Rec_1616696 Human_miRNA_ID_1933796,Human_miRNA_ID_1933797,Human_miRNA_ID_2197602,Human_miRNA_ID_2197603,Human_miRNA_ID_2936611,Human_miRNA_ID_2936612 Clinvar_Rec_570 RMVar_hsa_circ_41325,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353,RMVar_hsa_circ_333395,RMVar_hsa_circ_173355 96678 RMVar_ID_96678 Human_SNP_ID_581424718 m1A Human chr15 + 67181323 67181322 67181324 TACTACGAGCTGAACCAGCGCGTCGGGGAGACATTCCACGCCTCGCAGCCATCCATGACTGTGGA TACTACGAGCTGAACCAGCGCGTCGGGGAGAC__TCCACGCCTCGCAGCCATCCATGACTGTGGA CAT C SMAD3 Ensembl:ENSG00000166949 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:67181251..67181350 26863196 MeRIP-seq:(Medium) rs587776880 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9371101 Human_Splice_Rec_1616604,Human_Splice_Rec_1616636,Human_Splice_Rec_1616652,Human_Splice_Rec_1616664,Human_Splice_Rec_1616680,Human_Splice_Rec_1616690,Human_Splice_Rec_1616696 Human_miRNA_ID_1933796,Human_miRNA_ID_1933797,Human_miRNA_ID_2197602,Human_miRNA_ID_2197603,Human_miRNA_ID_2936611,Human_miRNA_ID_2936612 Clinvar_Rec_571 RMVar_hsa_circ_41325,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353,RMVar_hsa_circ_333395,RMVar_hsa_circ_173355 96679 RMVar_ID_96679 Human_SNP_ID_581424719 m1A Human chr15 + 67181323 67181323 67181323 TACTACGAGCTGAACCAGCGCGTCGGGGAGACATTCCACGCCTCGCAGCCATCCATGACTGTGGA TACTACGAGCTGAACCAGCGCGTCGGGGAGACGTTCCACGCCTCGCAGCCATCCATGACTGTGGA A G SMAD3 Ensembl:ENSG00000166949 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:67181251..67181350 26863196 MeRIP-seq:(Medium) rs201614771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371101 Human_Splice_Rec_1616604,Human_Splice_Rec_1616636,Human_Splice_Rec_1616652,Human_Splice_Rec_1616664,Human_Splice_Rec_1616680,Human_Splice_Rec_1616690,Human_Splice_Rec_1616696 Human_miRNA_ID_1933796,Human_miRNA_ID_1933797,Human_miRNA_ID_2197602,Human_miRNA_ID_2197603,Human_miRNA_ID_2936611,Human_miRNA_ID_2936612 RMVar_hsa_circ_41325,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353,RMVar_hsa_circ_333395,RMVar_hsa_circ_173355 96680 RMVar_ID_96680 Human_SNP_ID_581424720 m1A Human chr15 + 67181323 67181323 67181323 TACTACGAGCTGAACCAGCGCGTCGGGGAGACATTCCACGCCTCGCAGCCATCCATGACTGTGGA TACTACGAGCTGAACCAGCGCGTCGGGGAGACTTTCCACGCCTCGCAGCCATCCATGACTGTGGA A T SMAD3 Ensembl:ENSG00000166949 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:67181251..67181350 26863196 MeRIP-seq:(Medium) rs201614771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371101 Human_Splice_Rec_1616604,Human_Splice_Rec_1616636,Human_Splice_Rec_1616652,Human_Splice_Rec_1616664,Human_Splice_Rec_1616680,Human_Splice_Rec_1616690,Human_Splice_Rec_1616696 Human_miRNA_ID_1933796,Human_miRNA_ID_1933797,Human_miRNA_ID_2197602,Human_miRNA_ID_2197603,Human_miRNA_ID_2936611,Human_miRNA_ID_2936612 RMVar_hsa_circ_41325,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_43918,RMVar_hsa_circ_105881,RMVar_hsa_circ_173351,RMVar_hsa_circ_126261,RMVar_hsa_circ_173354,RMVar_hsa_circ_78296,RMVar_hsa_circ_173353,RMVar_hsa_circ_333395,RMVar_hsa_circ_173355 96681 RMVar_ID_96681 Human_SNP_ID_581426606 m1A Human chr15 - 67187461 67187461 67187461 AGCCTTTGACGAAGCTCATGCGGATGGTGCACATTCGGGTCAACTGGTAGACAGCCTCAAAGCCC AGCCTTTGACGAAGCTCATGCGGATGGTGCACTTTCGGGTCAACTGGTAGACAGCCTCAAAGCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:67187411..67190415 32194978 MeRIP-seq:(Medium) rs1294653592 Functional Loss SNV dbSNP153 33..33 33 - - - 96682 RMVar_ID_96682 Human_SNP_ID_581428338 m1A Human chr15 + 67194077 67194076 67194078 AGGACTGTTCACCAAGGGGGATACCAGCAGCAAGAGAGTGCACCCGTTTAGCCCTGGACCCTGTT AGGACTGTTCACCAAGGGGGATACCAGCAGCA__AGAGTGCACCCGTTTAGCCCTGGACCCTGTT AAG A SMAD3 Ensembl:ENSG00000166949 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:67194026..67194100 32194978 MeRIP-seq:(Medium) rs1347401300 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12564459 RMVar_hsa_circ_173354,RMVar_hsa_circ_78296 96683 RMVar_ID_96683 Human_SNP_ID_581502068 m1A Human chr15 - 67521396 67521396 67521396 GTTGCGGACGGCGCTGTAGGGCACGCAGAAGGAGGTCCAGTGCGGCAGGCGCCGCTGCAGCAGAT GTTGCGGACGGCGCTGTAGGGCACGCAGAAGGTGGTCCAGTGCGGCAGGCGCCGCTGCAGCAGAT T A IQCH-AS1 Ensembl:ENSG00000259673 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:67521216..67521852 32194978 MeRIP-seq:(Medium) rs752861436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886365 96684 RMVar_ID_96684 Human_SNP_ID_581507140 m1A Human chr15 - 67542772 67542772 67542772 GCGGCGCGCGCAGGCTGAGCTCCGGCCACCCGAGGCCGCGCGGACTGGCGGCGGCTGCGGCGGCG GCGGCGCGCGCAGGCTGAGCTCCGGCCACCCGGGGCCGCGCGGACTGGCGGCGGCTGCGGCGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:67542725..67542850;chr15:67542722..67543212 26863196 MeRIP-seq:(Medium) rs868684043 Functional Loss SNV dbSNP153 33..33 33 - - - 96685 RMVar_ID_96685 Human_SNP_ID_581630239 m1A Human chr15 - 68054381 68054381 68054381 CCTGGCAGCAGCGGCGCCGTCTCCGCGGCCGAATATTAGAAGTGAATTCGAGCTGCGCTTTACCT CCTGGCAGCAGCGGCGCCGTCTCCGCGGCCGATTATTAGAAGTGAATTCGAGCTGCGCTTTACCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:68054374..68054541 26863196 MeRIP-seq:(Medium) rs746533933 Functional Loss SNV dbSNP153 33..33 33 - - - 96686 RMVar_ID_96686 Human_SNP_ID_581634555 m1A Human chr15 + 68070478 68070476 68070479 AAGTGGGTAGCTGAGGGTGGAAAGTAATGATGAGGAGTTAAGTTGGAGCCTGAATGGCCAAGGCA AAGTGGGTAGCTGAGGGTGGAAAGTAATGAT___GAGTTAAGTTGGAGCCTGAATGGCCAAGGCA TGAG T PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:68070353..68070564 26863196 MeRIP-seq:(Medium) rs1395050305 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12566784 96687 RMVar_ID_96687 Human_SNP_ID_581635488 m1A Human chr15 + 68073694 68073694 68073694 CCTTGAAAGAACAGCATATATAAAAGTCCTGGAAGATGGAGAGTTGGTTAAAAGATTGGTTACGG CCTTGAAAGAACAGCATATATAAAAGTCCTGGTAGATGGAGAGTTGGTTAAAAGATTGGTTACGG A T PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:68073682..68073793 26863196 MeRIP-seq:(Medium) rs923009456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23662723 96688 RMVar_ID_96688 Human_SNP_ID_581635539 m1A Human chr15 - 68073885 68073880 68073885 CCACTCTAATTCAGAGTCTGCAAGAGACTCTTAACTTTTCTCCCTGCCTCCAATATTATCCTCTC CCACTCTAATTCAGAGTCTGCAAGAGACTCTT_____TTCTCCCTGCCTCCAATATTATCCTCTC AAAGTT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:68073879..68074153 26863196 MeRIP-seq:(Medium) rs1204995752 Functional Loss DEL dbSNP153 33..37 33 - - - 96689 RMVar_ID_96689 Human_SNP_ID_581635569 m1A Human chr15 + 68073988 68073988 68073988 AGGACTTGGTAAATAGATTGGAGGTGAACAAGAAGATGGTGTAGCAGCTTCTGGCATTGACGGGT AGGACTTGGTAAATAGATTGGAGGTGAACAAGCAGATGGTGTAGCAGCTTCTGGCATTGACGGGT A C PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:68073980..68074146 26863196 MeRIP-seq:(Medium) rs1222184661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12566814 96690 RMVar_ID_96690 Human_SNP_ID_581671920 m1A Human chr15 - 68213889 68213889 68213889 CCCACTGGGAAGAGAGGAAGAAGCCAGGTGGCAGGAGAGGCAGCAGCAGCAGCTGAACTCCATCC CCCACTGGGAAGAGAGGAAGAAGCCAGGTGGCGGGAGAGGCAGCAGCAGCAGCTGAACTCCATCC T C AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:68213887..68214317 26863196 MeRIP-seq:(Medium) rs901822436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3488930,Human_RBP_ID_22415157 RMVar_hsa_circ_302887,RMVar_hsa_circ_323593,RMVar_hsa_circ_173421,RMVar_hsa_circ_90064,RMVar_hsa_circ_272405,RMVar_hsa_circ_173422,RMVar_hsa_circ_173423 96691 RMVar_ID_96691 Human_SNP_ID_581673956 m1A Human chr15 + 68221726 68221726 68221726 GTCTGGGATGTGAGGAGCCCCTCTGCCCGGCCACCCCATCTGGGAGGTGAGAAGCGCCTCTGCCC GTCTGGGATGTGAGGAGCCCCTCTGCCCGGCCGCCCCATCTGGGAGGTGAGAAGCGCCTCTGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:68221720..68221864 26863196 MeRIP-seq:(Medium) rs1355697393 Functional Loss SNV dbSNP153 33..33 33 - - - 96692 RMVar_ID_96692 Human_SNP_ID_581674071 m1A Human chr15 + 68222006 68222006 68222006 CCCCTCTGCCCGGCTGCCCTGTCTGGGAGGTGAGAAGCGCCTCTGCCCGGCTGCCCATCGTCTGG CCCCTCTGCCCGGCTGCCCTGTCTGGGAGGTGGGAAGCGCCTCTGCCCGGCTGCCCATCGTCTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:68222003..68222195 26863196 MeRIP-seq:(Medium) rs1327371982 Functional Loss SNV dbSNP153 33..33 33 - - - 96693 RMVar_ID_96693 Human_SNP_ID_581676175 m1A Human chr15 + 68229461 68229461 68229461 GCGTCACGTGGCGGGTCCCGAGGCCCCAGCGCACAGGCGCCTAGCCCGCCCTCTCACCCCGGCGC GCGTCACGTGGCGGGTCCCGAGGCCCCAGCGCTCAGGCGCCTAGCCCGCCCTCTCACCCCGGCGC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:68229459..68229706 26863410 MeRIP-seq:(Medium) rs1340459496 Functional Loss SNV dbSNP153 33..33 33 - - - 96694 RMVar_ID_96694 Human_SNP_ID_581676246 m1A Human chr15 - 68229584 68229584 68229584 AAAGGCAGGGCCGAGGGGCCTGCGGGGCAGCCATGGAGGCGACGCGGAGGCGGCAGCACCTGGGA AAAGGCAGGGCCGAGGGGCCTGCGGGGCAGCCGTGGAGGCGACGCGGAGGCGGCAGCACCTGGGA T C AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding start codon,start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:68229461..68229678 26863196 MeRIP-seq:(Medium) rs1555440206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232077,Human_RBP_ID_4330313,Human_RBP_ID_18418390,Human_RBP_ID_22192877 Human_Splice_Rec_1617491,Human_Splice_Rec_1617503,Human_Splice_Rec_1617507,Human_Splice_Rec_1617557,Human_Splice_Rec_1617569,Human_Splice_Rec_1617585,Human_Splice_Rec_1617599,Human_Splice_Rec_1617607,Human_Splice_Rec_1617641,Human_Splice_Rec_1617657,Human_Splice_Rec_1617675,Human_Splice_Rec_1617687,Human_Splice_Rec_1617697,Human_Splice_Rec_1617707,Human_Splice_Rec_1617729,Human_Splice_Rec_1617747 RMVar_hsa_circ_90064,RMVar_hsa_circ_108406,RMVar_hsa_circ_173423,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424,RMVar_hsa_circ_173427 96695 RMVar_ID_96695 Human_SNP_ID_581676293 m1A Human chr15 - 68229685 68229676 68229686 GAGGGCCGCGCGCTCTCGCCGGCCCGCCCCGAACCGCCCCGCGCTGGGAATTTGCGGCGGCCTCC GAGGGCCGCGCGCTCTCGCCGGCCCGCCCCG__________CGCTGGGAATTTGCGGCGGCCTCC GCGGGGCGGTT G AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:68229617..68229718 26863410 MeRIP-seq:(Medium) rs1481647841 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_4342786 Human_miRNA_ID_2250216,Human_miRNA_ID_3066060 RMVar_hsa_circ_90064,RMVar_hsa_circ_108406,RMVar_hsa_circ_173423,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424,RMVar_hsa_circ_173427 96696 RMVar_ID_96696 Human_SNP_ID_581676301 m1A Human chr15 - 68229685 68229685 68229685 GAGGGCCGCGCGCTCTCGCCGGCCCGCCCCGAACCGCCCCGCGCTGGGAATTTGCGGCGGCCTCC GAGGGCCGCGCGCTCTCGCCGGCCCGCCCCGAGCCGCCCCGCGCTGGGAATTTGCGGCGGCCTCC T C AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:68229617..68229718 26863410 MeRIP-seq:(Medium) rs555985698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342786 Human_miRNA_ID_2250216,Human_miRNA_ID_3066060 RMVar_hsa_circ_90064,RMVar_hsa_circ_108406,RMVar_hsa_circ_173423,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424,RMVar_hsa_circ_173427 96697 RMVar_ID_96697 Human_SNP_ID_581687955 m1A Human chr15 - 68277864 68277864 68277864 TCCGCCGAGCTCAGAAGTGCCAGGCGCTGCCAACGGCCCCGGAGATCCTCGCGTAGGGGCCCCCG TCCGCCGAGCTCAGAAGTGCCAGGCGCTGCCAGCGGCCCCGGAGATCCTCGCGTAGGGGCCCCCG T C AC107871.2 Ensembl:ENSG00000260657 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:68277815..68277958 26863196 MeRIP-seq:(Medium) rs1351386678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1617755 96698 RMVar_ID_96698 Human_SNP_ID_581688043 m1A Human chr15 - 68278101 68278101 68278101 CATGGCGGACGCCGCCCCGGGCCTCAGGCCGGACCCCTCCTTCCTGCGGGATGCGACAGGCGCGT CATGGCGGACGCCGCCCCGGGCCTCAGGCCGGGCCCCTCCTTCCTGCGGGATGCGACAGGCGCGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:68278001..68278251 26863410 MeRIP-seq:(Medium) rs1317263991 Functional Loss SNV dbSNP153 33..33 33 - - - 96699 RMVar_ID_96699 Human_SNP_ID_581812328 m1A Human chr15 + 68780426 68780426 68780426 AAAAAGGCTGCCATACCACCAAGCTCTTCTTCATCTTCCTCGTCATCTACCTCTCCATCGTTATA AAAAAGGCTGCCATACCACCAAGCTCTTCTTCGTCTTCCTCGTCATCTACCTCTCCATCGTTATA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:68780401..68780475 26863196 MeRIP-seq:(Medium) rs1057028481 Functional Loss SNV dbSNP153 33..33 33 - - - 96700 RMVar_ID_96700 Human_SNP_ID_581812979 m1A Human chr15 + 68783034 68783034 68783034 TCCTCGTCCTCCTCGTCTTCCACTACCTGAGCATCTTCATCATACTCCTCCTCTGTGCAATCGAA TCCTCGTCCTCCTCGTCTTCCACTACCTGAGCGTCTTCATCATACTCCTCCTCTGTGCAATCGAA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:68782951..68783075;chr15:68782905..68784600;chr15:68782889..68787215 26863196 MeRIP-seq:(Medium) rs1295908628 Functional Loss SNV dbSNP153 33..33 33 - - - 96701 RMVar_ID_96701 Human_SNP_ID_581813323 m1A Human chr15 + 68784383 68784383 68784383 GCCTCAGCTGGGCCCCTGCAGCCCTGGGCCGCACCCTGTCACCCACCATCCTCATCCTCCTCCTC GCCTCAGCTGGGCCCCTGCAGCCCTGGGCCGCGCCCTGTCACCCACCATCCTCATCCTCCTCCTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr15:68784376..68784550;chr15:68784376..68784525 26863196,32194978 MeRIP-seq:(Medium) rs943159325 Functional Loss SNV dbSNP153 33..33 33 - - - 96702 RMVar_ID_96702 Human_SNP_ID_581814060 m1A Human chr15 - 68787475 68787475 68787475 GGGGCCTGGAAGTATTGGCAGAAAAGTGTCCGAACCTCACGCATCTAAATTTAAGTGGCAACAAA GGGGCCTGGAAGTATTGGCAGAAAAGTGTCCGTACCTCACGCATCTAAATTTAAGTGGCAACAAA T A ANP32A Ensembl:ENSG00000140350 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:68787426..68787500 26863196 MeRIP-seq:(Medium) rs545923966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462401,Human_RBP_ID_1001745,Human_RBP_ID_1832883,Human_RBP_ID_2452457,Human_RBP_ID_5112923,Human_RBP_ID_6454599,Human_RBP_ID_8421372,Human_RBP_ID_9371116,Human_RBP_ID_12570251,Human_RBP_ID_17366119,Human_RBP_ID_17483473,Human_RBP_ID_18666753,Human_RBP_ID_22930603,Human_RBP_ID_24368459,Human_RBP_ID_26327693,Human_RBP_ID_26933574,Human_RBP_ID_27653907 Human_Splice_Rec_1617988,Human_Splice_Rec_1617989,Human_Splice_Rec_1618000,Human_Splice_Rec_1618001,Human_Splice_Rec_1618014,Human_Splice_Rec_1618015,Human_Splice_Rec_1618026,Human_Splice_Rec_1618027,Human_Splice_Rec_1618038,Human_Splice_Rec_1618039,Human_Splice_Rec_1618046,Human_Splice_Rec_1618047,Human_Splice_Rec_1618052,Human_Splice_Rec_1618056 Human_miRNA_ID_2007373 RMVar_hsa_circ_12259,RMVar_hsa_circ_101065,RMVar_hsa_circ_173440,RMVar_hsa_circ_293729 96703 RMVar_ID_96703 Human_SNP_ID_581814061 m1A Human chr15 - 68787475 68787475 68787475 GGGGCCTGGAAGTATTGGCAGAAAAGTGTCCGAACCTCACGCATCTAAATTTAAGTGGCAACAAA GGGGCCTGGAAGTATTGGCAGAAAAGTGTCCGGACCTCACGCATCTAAATTTAAGTGGCAACAAA T C ANP32A Ensembl:ENSG00000140350 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:68787426..68787500 26863196 MeRIP-seq:(Medium) rs545923966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462401,Human_RBP_ID_1001745,Human_RBP_ID_1832883,Human_RBP_ID_2452457,Human_RBP_ID_5112923,Human_RBP_ID_6454599,Human_RBP_ID_8421372,Human_RBP_ID_9371116,Human_RBP_ID_12570251,Human_RBP_ID_17366119,Human_RBP_ID_17483473,Human_RBP_ID_18666753,Human_RBP_ID_22930603,Human_RBP_ID_24368459,Human_RBP_ID_26327693,Human_RBP_ID_26933574,Human_RBP_ID_27653907 Human_Splice_Rec_1617988,Human_Splice_Rec_1617989,Human_Splice_Rec_1618000,Human_Splice_Rec_1618001,Human_Splice_Rec_1618014,Human_Splice_Rec_1618015,Human_Splice_Rec_1618026,Human_Splice_Rec_1618027,Human_Splice_Rec_1618038,Human_Splice_Rec_1618039,Human_Splice_Rec_1618046,Human_Splice_Rec_1618047,Human_Splice_Rec_1618052,Human_Splice_Rec_1618056 Human_miRNA_ID_2007373 RMVar_hsa_circ_12259,RMVar_hsa_circ_101065,RMVar_hsa_circ_173440,RMVar_hsa_circ_293729 96704 RMVar_ID_96704 Human_SNP_ID_581822750 m1A Human chr15 - 68820763 68820759 68820763 AATTCCGCCGGCGCGGGAGCCTCTGCAGAGAGAGAGCGCGAGAGATGGAGATGGGCAGACGGATT AATTCCGCCGGCGCGGGAGCCTCTGCAGAGAG____CGCGAGAGATGGAGATGGGCAGACGGATT GCTCT G ANP32A Ensembl:ENSG00000140350 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:68820714..68820875 26863196 MeRIP-seq:(Medium) rs772512853 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_232622,Human_RBP_ID_759543,Human_RBP_ID_1507330,Human_RBP_ID_1832922,Human_RBP_ID_3480858,Human_RBP_ID_4342789,Human_RBP_ID_5464609,Human_RBP_ID_6454869,Human_RBP_ID_8421427,Human_RBP_ID_9283698,Human_RBP_ID_9324327,Human_RBP_ID_17870189,Human_RBP_ID_18418391,Human_RBP_ID_22047552,Human_RBP_ID_22192966,Human_RBP_ID_22440362,Human_RBP_ID_23663415,Human_RBP_ID_26326894,Human_RBP_ID_26933654,Human_RBP_ID_27233439 Human_Splice_Rec_1617985,Human_Splice_Rec_1617997,Human_Splice_Rec_1618035,Human_Splice_Rec_1618049 96705 RMVar_ID_96705 Human_SNP_ID_581822753 m1A Human chr15 - 68820763 68820763 68820763 AATTCCGCCGGCGCGGGAGCCTCTGCAGAGAGAGAGCGCGAGAGATGGAGATGGGCAGACGGATT AATTCCGCCGGCGCGGGAGCCTCTGCAGAGAGCGAGCGCGAGAGATGGAGATGGGCAGACGGATT T G ANP32A Ensembl:ENSG00000140350 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:68820714..68820875 26863196 MeRIP-seq:(Medium) rs747530650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232622,Human_RBP_ID_759543,Human_RBP_ID_1507330,Human_RBP_ID_1832922,Human_RBP_ID_3480858,Human_RBP_ID_4342789,Human_RBP_ID_5464609,Human_RBP_ID_6454869,Human_RBP_ID_8421427,Human_RBP_ID_9283698,Human_RBP_ID_9324327,Human_RBP_ID_17870189,Human_RBP_ID_18418391,Human_RBP_ID_22047552,Human_RBP_ID_22192966,Human_RBP_ID_22440362,Human_RBP_ID_23663415,Human_RBP_ID_26326894,Human_RBP_ID_26933654,Human_RBP_ID_27233439 Human_Splice_Rec_1617985,Human_Splice_Rec_1617997,Human_Splice_Rec_1618035,Human_Splice_Rec_1618049 96706 RMVar_ID_96706 Human_SNP_ID_581822759 m1A Human chr15 + 68820774 68820774 68820774 CCATCTCCATCTCTCGCGCTCTCTCTCTGCAGAGGCTCCCGCGCCGGCGGAATTCAATCAATAAA CCATCTCCATCTCTCGCGCTCTCTCTCTGCAGCGGCTCCCGCGCCGGCGGAATTCAATCAATAAA A C SPESP1 Ensembl:ENSG00000258484 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:68820726..68820850 32194978 MeRIP-seq:(Medium) rs1183184506 Functional Loss SNV dbSNP153 33..33 33 - - - 96707 RMVar_ID_96707 Human_SNP_ID_581957098 m1A Human chr15 + 69386256 69386254 69386257 TCACATACATCACACACACACACCACACACACACATCACACACACCACATACATACACACACACC TCACATACATCACACACACACACCACACACA___ATCACACACACCACATACATACACACACACC ACAC A PAQR5 Ensembl:ENSG00000137819 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:69386254..69386337 26863196 MeRIP-seq:(Medium) rs1293686623 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2452701 RMVar_hsa_circ_91134,RMVar_hsa_circ_122840,RMVar_hsa_circ_92426,RMVar_hsa_circ_111302,RMVar_hsa_circ_173454,RMVar_hsa_circ_173455,RMVar_hsa_circ_173453,RMVar_hsa_circ_86484,RMVar_hsa_circ_99633,RMVar_hsa_circ_173457,RMVar_hsa_circ_173458,RMVar_hsa_circ_314482,RMVar_hsa_circ_370317,RMVar_hsa_circ_173461,RMVar_hsa_circ_173462,RMVar_hsa_circ_173463,RMVar_hsa_circ_353436,RMVar_hsa_circ_173464 96708 RMVar_ID_96708 Human_SNP_ID_581963912 m1A Human chr15 + 69414474 69414474 69414474 TTGGGCGGCGTGGAGCCTGCTGCCATGAAGTCAGCGTGAGTACGAGGCCGCCGAGCAGGGAGAGA TTGGGCGGCGTGGAGCCTGCTGCCATGAAGTCGGCGTGAGTACGAGGCCGCCGAGCAGGGAGAGA A G KIF23 Ensembl:ENSG00000137807 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:69414339..69416012 26863196 MeRIP-seq:(Medium) rs1343634482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342792,Human_RBP_ID_8803917,Human_RBP_ID_19068467 Human_Splice_Rec_1618445,Human_Splice_Rec_1618489,Human_Splice_Rec_1618525,Human_Splice_Rec_1618569,Human_Splice_Rec_1618611,Human_Splice_Rec_1618651,Human_Splice_Rec_1618679,Human_Splice_Rec_1618723,Human_Splice_Rec_1618765 96709 RMVar_ID_96709 Human_SNP_ID_581964256 m1A Human chr15 + 69416004 69416004 69416004 TTATTTTTTAATCTATGACCAGGAGAGCTAAGACACCCCGGAAACCTACCGTGAAAAAAGGGTCC TTATTTTTTAATCTATGACCAGGAGAGCTAAGGCACCCCGGAAACCTACCGTGAAAAAAGGGTCC A G KIF23 Ensembl:ENSG00000137807 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:69414345..69421665 32194978 MeRIP-seq:(Medium) rs770423663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4330880,Human_RBP_ID_12571788,Human_RBP_ID_22930681,Human_RBP_ID_25183768 Human_Splice_Rec_1618446,Human_Splice_Rec_1618447,Human_Splice_Rec_1618490,Human_Splice_Rec_1618491,Human_Splice_Rec_1618526,Human_Splice_Rec_1618527,Human_Splice_Rec_1618570,Human_Splice_Rec_1618571,Human_Splice_Rec_1618612,Human_Splice_Rec_1618613,Human_Splice_Rec_1618652,Human_Splice_Rec_1618653,Human_Splice_Rec_1618680,Human_Splice_Rec_1618681,Human_Splice_Rec_1618724,Human_Splice_Rec_1618725,Human_Splice_Rec_1618766,Human_Splice_Rec_1618767 RMVar_hsa_circ_62217,RMVar_hsa_circ_352176,RMVar_hsa_circ_127287,RMVar_hsa_circ_173468 96710 RMVar_ID_96710 Human_SNP_ID_581964257 m1A Human chr15 + 69416004 69416004 69416004 TTATTTTTTAATCTATGACCAGGAGAGCTAAGACACCCCGGAAACCTACCGTGAAAAAAGGGTCC TTATTTTTTAATCTATGACCAGGAGAGCTAAGTCACCCCGGAAACCTACCGTGAAAAAAGGGTCC A T KIF23 Ensembl:ENSG00000137807 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:69414345..69421665 32194978 MeRIP-seq:(Medium) rs770423663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4330880,Human_RBP_ID_12571788,Human_RBP_ID_22930681,Human_RBP_ID_25183768 Human_Splice_Rec_1618446,Human_Splice_Rec_1618447,Human_Splice_Rec_1618490,Human_Splice_Rec_1618491,Human_Splice_Rec_1618526,Human_Splice_Rec_1618527,Human_Splice_Rec_1618570,Human_Splice_Rec_1618571,Human_Splice_Rec_1618612,Human_Splice_Rec_1618613,Human_Splice_Rec_1618652,Human_Splice_Rec_1618653,Human_Splice_Rec_1618680,Human_Splice_Rec_1618681,Human_Splice_Rec_1618724,Human_Splice_Rec_1618725,Human_Splice_Rec_1618766,Human_Splice_Rec_1618767 RMVar_hsa_circ_62217,RMVar_hsa_circ_352176,RMVar_hsa_circ_127287,RMVar_hsa_circ_173468 96711 RMVar_ID_96711 Human_SNP_ID_581967890 m1A Human chr15 + 69431191 69431191 69431191 GAGGAGAAGCAGTTTTAGGAGCAGGTATAGGCAGGTAATGAGTTGTATTTGAAATGTTCAATTTA GAGGAGAAGCAGTTTTAGGAGCAGGTATAGGCGGGTAATGAGTTGTATTTGAAATGTTCAATTTA A G KIF23 Ensembl:ENSG00000137807 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:69431184..69431249 26863196 MeRIP-seq:(Medium) rs1200396067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6455538 RMVar_hsa_circ_22235,RMVar_hsa_circ_310800,RMVar_hsa_circ_334626,RMVar_hsa_circ_352783,RMVar_hsa_circ_68276,RMVar_hsa_circ_173473,RMVar_hsa_circ_104514,RMVar_hsa_circ_31243,RMVar_hsa_circ_173474,RMVar_hsa_circ_66530,RMVar_hsa_circ_310036,RMVar_hsa_circ_173475 96712 RMVar_ID_96712 Human_SNP_ID_581973167 m1A Human chr15 + 69452861 69452861 69452861 AGCTGCCGCCAAGGTGCTCGGTCCTTCCGAGGAAGCTAAGGCTGCGTTGGGGTGAGGCCCTCACT AGCTGCCGCCAAGGTGCTCGGTCCTTCCGAGGGAGCTAAGGCTGCGTTGGGGTGAGGCCCTCACT A G RPLP1 Ensembl:ENSG00000137818 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs901781857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232116,Human_RBP_ID_269647,Human_RBP_ID_462525,Human_RBP_ID_758914,Human_RBP_ID_814830,Human_RBP_ID_886600,Human_RBP_ID_1001806,Human_RBP_ID_1175497,Human_RBP_ID_1507517,Human_RBP_ID_1833076,Human_RBP_ID_3481069,Human_RBP_ID_4330964,Human_RBP_ID_5178570,Human_RBP_ID_5274586,Human_RBP_ID_5418695,Human_RBP_ID_5439806,Human_RBP_ID_5464170,Human_RBP_ID_5494618,Human_RBP_ID_6455731,Human_RBP_ID_8421546,Human_RBP_ID_8801729,Human_RBP_ID_17865424,Human_RBP_ID_18207321,Human_RBP_ID_18666961,Human_RBP_ID_20004191,Human_RBP_ID_22193013,Human_RBP_ID_22799123,Human_RBP_ID_23127537,Human_RBP_ID_23663736,Human_RBP_ID_24411986,Human_RBP_ID_24474430,Human_RBP_ID_25159794,Human_RBP_ID_26435643,Human_RBP_ID_26933721,Human_RBP_ID_27233489,Human_RBP_ID_27436526 RMVar_hsa_circ_109341,RMVar_hsa_circ_114312,RMVar_hsa_circ_173479,RMVar_hsa_circ_173480 96713 RMVar_ID_96713 Human_SNP_ID_581973168 m1A Human chr15 + 69452861 69452861 69452861 AGCTGCCGCCAAGGTGCTCGGTCCTTCCGAGGAAGCTAAGGCTGCGTTGGGGTGAGGCCCTCACT AGCTGCCGCCAAGGTGCTCGGTCCTTCCGAGGTAGCTAAGGCTGCGTTGGGGTGAGGCCCTCACT A T RPLP1 Ensembl:ENSG00000137818 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs901781857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232116,Human_RBP_ID_269647,Human_RBP_ID_462525,Human_RBP_ID_758914,Human_RBP_ID_814830,Human_RBP_ID_886600,Human_RBP_ID_1001806,Human_RBP_ID_1175497,Human_RBP_ID_1507517,Human_RBP_ID_1833076,Human_RBP_ID_3481069,Human_RBP_ID_4330964,Human_RBP_ID_5178570,Human_RBP_ID_5274586,Human_RBP_ID_5418695,Human_RBP_ID_5439806,Human_RBP_ID_5464170,Human_RBP_ID_5494618,Human_RBP_ID_6455731,Human_RBP_ID_8421546,Human_RBP_ID_8801729,Human_RBP_ID_17865424,Human_RBP_ID_18207321,Human_RBP_ID_18666961,Human_RBP_ID_20004191,Human_RBP_ID_22193013,Human_RBP_ID_22799123,Human_RBP_ID_23127537,Human_RBP_ID_23663736,Human_RBP_ID_24411986,Human_RBP_ID_24474430,Human_RBP_ID_25159794,Human_RBP_ID_26435643,Human_RBP_ID_26933721,Human_RBP_ID_27233489,Human_RBP_ID_27436526 RMVar_hsa_circ_109341,RMVar_hsa_circ_114312,RMVar_hsa_circ_173479,RMVar_hsa_circ_173480 96714 RMVar_ID_96714 Human_SNP_ID_581973180 m1A Human chr15 - 69452881 69452881 69452881 CGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCACCCCAACGCAGCCTTAGCTTCCTCGGAAGGAC CGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCGCCCCAACGCAGCCTTAGCTTCCTCGGAAGGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:69452801..69453032;chr15:69452826..69453066;chr15:69452826..69453068;chr15:69452826..69453025 26863196 MeRIP-seq:(Medium) rs1814763 Functional Loss SNV dbSNP153 33..33 33 - - - 96715 RMVar_ID_96715 Human_SNP_ID_581973181 m1A Human chr15 - 69452881 69452881 69452881 CGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCACCCCAACGCAGCCTTAGCTTCCTCGGAAGGAC CGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCCCCCCAACGCAGCCTTAGCTTCCTCGGAAGGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:69452801..69453032;chr15:69452826..69453066;chr15:69452826..69453068;chr15:69452826..69453025 26863196 MeRIP-seq:(Medium) rs1814763 Functional Loss SNV dbSNP153 33..33 33 - - - 96716 RMVar_ID_96716 Human_SNP_ID_581973189 m1A Human chr15 - 69452893 69452893 69452893 CGCTGCCGGACGCGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT CGCTGCCGGACGCGGTGCTAGTCGCCGGATGATGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:69452826..69453230 32194978 MeRIP-seq:(Medium) rs552626514 Functional Loss SNV dbSNP153 33..33 33 - - - 96717 RMVar_ID_96717 Human_SNP_ID_581973190 m1A Human chr15 - 69452893 69452893 69452893 CGCTGCCGGACGCGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT CGCTGCCGGACGCGGTGCTAGTCGCCGGATGACGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:69452826..69453230 32194978 MeRIP-seq:(Medium) rs552626514 Functional Loss SNV dbSNP153 33..33 33 - - - 96718 RMVar_ID_96718 Human_SNP_ID_581973213 m1A Human chr15 + 69452936 69452936 69452936 ACTAGCACCGCGTCCGGCAGCGCCAGCCCTACACTCGCCCGCGCCATGGCCTCTGTCTCCGAGCT ACTAGCACCGCGTCCGGCAGCGCCAGCCCTACGCTCGCCCGCGCCATGGCCTCTGTCTCCGAGCT A G RPLP1 Ensembl:ENSG00000137818 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T cell line,total RNA;HEK293T,H2O2 treatment chr15:69452826..69453054;chr15:69452882..69452982 26863196,26863410 MeRIP-seq:(Medium) rs1435704060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232116,Human_RBP_ID_462526,Human_RBP_ID_758914,Human_RBP_ID_814830,Human_RBP_ID_886600,Human_RBP_ID_1001806,Human_RBP_ID_1507517,Human_RBP_ID_1833078,Human_RBP_ID_3481071,Human_RBP_ID_4330964,Human_RBP_ID_5178571,Human_RBP_ID_5439808,Human_RBP_ID_8421546,Human_RBP_ID_12572630,Human_RBP_ID_17652157,Human_RBP_ID_17865426,Human_RBP_ID_18666964,Human_RBP_ID_22930771,Human_RBP_ID_24474433,Human_RBP_ID_26435644,Human_RBP_ID_26933721,Human_RBP_ID_27233489,Human_RBP_ID_27436530,Human_RBP_ID_27559600 Human_Splice_Rec_1618845,Human_Splice_Rec_1618849,Human_Splice_Rec_1618855,Human_Splice_Rec_1618859 Human_miRNA_ID_2250217,Human_miRNA_ID_2975749 RMVar_hsa_circ_109341,RMVar_hsa_circ_114312,RMVar_hsa_circ_173479,RMVar_hsa_circ_173480 96719 RMVar_ID_96719 Human_SNP_ID_581973229 m1A Human chr15 - 69452955 69452955 69452955 GGCCGAGTAGATGCAGGCGAGCTCGGAGACAGAGGCCATGGCGCGGGCGAGTGTAGGGCTGGCGC GGCCGAGTAGATGCAGGCGAGCTCGGAGACAGCGGCCATGGCGCGGGCGAGTGTAGGGCTGGCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:69452826..69453063 26863196 MeRIP-seq:(Medium) rs766664754 Functional Loss SNV dbSNP153 33..33 33 - - - 96720 RMVar_ID_96720 Human_SNP_ID_581973688 m1A Human chr15 - 69454199 69454199 69454199 GTGAAACCCCGTCACTACTAAACACACACACAAAAATTAGCCAGGCATGGTGGCGCACGCCTGTA GTGAAACCCCGTCACTACTAAACACACACACAGAAATTAGCCAGGCATGGTGGCGCACGCCTGTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:69454170..69454270 32194978 MeRIP-seq:(Medium) rs920502786 Functional Loss SNV dbSNP153 33..33 33 - - - 96721 RMVar_ID_96721 Human_SNP_ID_581973689 m1A Human chr15 - 69454199 69454199 69454199 GTGAAACCCCGTCACTACTAAACACACACACAAAAATTAGCCAGGCATGGTGGCGCACGCCTGTA GTGAAACCCCGTCACTACTAAACACACACACACAAATTAGCCAGGCATGGTGGCGCACGCCTGTA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:69454170..69454270 32194978 MeRIP-seq:(Medium) rs920502786 Functional Loss SNV dbSNP153 33..33 33 - - - 96722 RMVar_ID_96722 Human_SNP_ID_582115276 m1A Human chr15 - 70049287 70049287 70049287 AGATGGGGGCCCGTCCAGGCGGACACCCGCAGAAATGGAGCTTTCTGTGGTCTCTTGCACTCTGG AGATGGGGGCCCGTCCAGGCGGACACCCGCAGCAATGGAGCTTTCTGTGGTCTCTTGCACTCTGG T G TLE3 Ensembl:ENSG00000140332 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70049198..70049438 32194978 MeRIP-seq:(Medium) rs925501825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462603,Human_RBP_ID_1279382,Human_RBP_ID_8421617,Human_RBP_ID_23663873 Human_miRNA_ID_264890 96723 RMVar_ID_96723 Human_SNP_ID_582117859 m1A Human chr15 + 70057561 70057561 70057561 GGTGGGATGTTGTGGAGGCCGGCGTAGGCGCCAGGACTGGTGAGGGAGCCGTTCATCTCATGGTG GGTGGGATGTTGTGGAGGCCGGCGTAGGCGCCCGGACTGGTGAGGGAGCCGTTCATCTCATGGTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr15:70057514..70057719;chr15:70057451..70057615 26863196 MeRIP-seq:(Medium) rs1276107253 Functional Loss SNV dbSNP153 33..33 33 - - - 96724 RMVar_ID_96724 Human_SNP_ID_582117901 m1A Human chr15 + 70057637 70057637 70057637 CGAAGGGCGCCGCATAGGAGCTGGTGATGGAGATGGGCGTGCGCAGAGCCGAGGCTGCGAGGGGT CGAAGGGCGCCGCATAGGAGCTGGTGATGGAGTTGGGCGTGCGCAGAGCCGAGGCTGCGAGGGGT A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:70057541..70057723 26863196 MeRIP-seq:(Medium) rs1322173191 Functional Loss SNV dbSNP153 33..33 33 - - - 96725 RMVar_ID_96725 Human_SNP_ID_582118129 m1A Human chr15 - 70058276 70058276 70058276 GCATCTCCCCTCTTCAGAACGACAAATCCTCCACCCCTGGGCTCAAGTCCAACACACCAACCCCA GCATCTCCCCTCTTCAGAACGACAAATCCTCCGCCCCTGGGCTCAAGTCCAACACACCAACCCCA T C TLE3 Ensembl:ENSG00000140332 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:70058226..70058275 26863196 MeRIP-seq:(Medium) rs1227851981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1279387,Human_RBP_ID_1363969,Human_RBP_ID_6456153,Human_RBP_ID_8801804,Human_RBP_ID_9283274 Human_Splice_Rec_1619528,Human_Splice_Rec_1619566,Human_Splice_Rec_1619600,Human_Splice_Rec_1619638,Human_Splice_Rec_1619639,Human_Splice_Rec_1619676,Human_Splice_Rec_1619714,Human_Splice_Rec_1619752,Human_Splice_Rec_1619790,Human_Splice_Rec_1619826,Human_Splice_Rec_1619862,Human_Splice_Rec_1619900,Human_Splice_Rec_1619938,Human_Splice_Rec_1619974,Human_Splice_Rec_1619975,Human_Splice_Rec_1620010,Human_Splice_Rec_1620048,Human_Splice_Rec_1620102,Human_Splice_Rec_1620140,Human_Splice_Rec_1620162 RMVar_hsa_circ_40774,RMVar_hsa_circ_33823 96726 RMVar_ID_96726 Human_SNP_ID_582128329 m1A Human chr15 + 70096831 70096831 70096831 GGCAGGGAGGGGTCGTGATTCCGAGAGCGTGGAAGCGCCGAGAGCCCGGGCCGGGGAGGTGCGGG GGCAGGGAGGGGTCGTGATTCCGAGAGCGTGGGAGCGCCGAGAGCCCGGGCCGGGGAGGTGCGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:70096801..70097241 26863196 MeRIP-seq:(Medium) rs761062149 Functional Loss SNV dbSNP153 33..33 33 - - - 96727 RMVar_ID_96727 Human_SNP_ID_582128588 m1A Human chr15 + 70097445 70097445 70097445 CTCGGAGAGGAGAGCCTGCTGTTCCGTCTGCTACTGCCGCTGCCGCCGCCGCCGCCGCCGCTGCA CTCGGAGAGGAGAGCCTGCTGTTCCGTCTGCTGCTGCCGCTGCCGCCGCCGCCGCCGCCGCTGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:70097426..70097450 26863196 MeRIP-seq:(Medium) rs1482218943 Functional Loss SNV dbSNP153 33..33 33 - - - 96728 RMVar_ID_96728 Human_SNP_ID_582128646 m1A Human chr15 + 70097574 70097574 70097574 CTAAGTCCAGCGGGCACGGGAAGCCTCCGCAAAGGGTTCTCGCTGCTCCCAGCTTGAGCACCGCG CTAAGTCCAGCGGGCACGGGAAGCCTCCGCAAGGGGTTCTCGCTGCTCCCAGCTTGAGCACCGCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70097526..70097777 32194978 MeRIP-seq:(Medium) rs1453353197 Functional Loss SNV dbSNP153 33..33 33 - - - 96729 RMVar_ID_96729 Human_SNP_ID_582264701 m1A Human chr15 - 70655349 70655349 70655349 GTGGCAGGTGCCTGTAGTCCCAGGTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACCTGGGA GTGGCAGGTGCCTGTAGTCCCAGGTACTCGGGGGGCTGAGACAGGAGAATCGCTTGAACCTGGGA T C UACA Ensembl:ENSG00000137831 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs567189507 Functional Loss SNV dbSNP153 33..33 33 - - - 96730 RMVar_ID_96730 Human_SNP_ID_582306885 m1A Human chr15 - 70832055 70832055 70832055 TTTCATGGCCATGAGAGGAGCAGGGCCTGTGTATAAATACCTTCTATTTTTAATACAAGCTCCAC TTTCATGGCCATGAGAGGAGCAGGGCCTGTGTGTAAATACCTTCTATTTTTAATACAAGCTCCAC T C LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:70832005..70832105 32194978 MeRIP-seq:(Medium) rs1187359774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462691,Human_RBP_ID_6457116,Human_RBP_ID_8081042,Human_RBP_ID_17250928,Human_RBP_ID_17865609 Human_miRNA_ID_2350547 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96731 RMVar_ID_96731 Human_SNP_ID_582306896 m1A Human chr15 - 70832077 70832077 70832077 GGGTCCTGACAACACCAGAGGATTTCATGGCCATGAGAGGAGCAGGGCCTGTGTATAAATACCTT GGGTCCTGACAACACCAGAGGATTTCATGGCCTTGAGAGGAGCAGGGCCTGTGTATAAATACCTT T A LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70832026..70832275 32194978 MeRIP-seq:(Medium) rs779582644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2381110,Human_miRNA_ID_2393527,Human_miRNA_ID_3024125 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96732 RMVar_ID_96732 Human_SNP_ID_582306897 m1A Human chr15 - 70832077 70832077 70832077 GGGTCCTGACAACACCAGAGGATTTCATGGCCATGAGAGGAGCAGGGCCTGTGTATAAATACCTT GGGTCCTGACAACACCAGAGGATTTCATGGCCGTGAGAGGAGCAGGGCCTGTGTATAAATACCTT T C LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70832026..70832275 32194978 MeRIP-seq:(Medium) rs779582644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2381110,Human_miRNA_ID_2393527,Human_miRNA_ID_3024125 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96733 RMVar_ID_96733 Human_SNP_ID_582307038 m1A Human chr15 - 70832452 70832451 70832452 CCCTATGGCGGGCCGACGGCACGCGGCCACCAACAAGCTCAGCCCGTCTGGCCACCAGAATCTCT CCCTATGGCGGGCCGACGGCACGCGGCCACCA_CAAGCTCAGCCCGTCTGGCCACCAGAATCTCT GT G LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:70832302..70832452;chr15:70832402..70832538;chr15:70832401..70832551 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1567019621 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4331411 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96734 RMVar_ID_96734 Human_SNP_ID_582307980 m1A Human chr15 + 70836505 70836505 70836505 CGCTCGTTCTCACCTCCACTTGCAGTGGTGCCACTGAGACCAGAAGGAGACACCGGGTGTTAGGG CGCTCGTTCTCACCTCCACTTGCAGTGGTGCCGCTGAGACCAGAAGGAGACACCGGGTGTTAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:70836462..70851493 26863196 MeRIP-seq:(Medium) rs576300460 Functional Loss SNV dbSNP153 33..33 33 - - - 96735 RMVar_ID_96735 Human_SNP_ID_582311536 m1A Human chr15 - 70851699 70851699 70851699 CTCCCTCACAGGAATAGGAGCTCGGTGAATTCAAGGACCATGCTTGCTTCGTTCATTGTATCTTC CTCCCTCACAGGAATAGGAGCTCGGTGAATTCGAGGACCATGCTTGCTTCGTTCATTGTATCTTC T C LARP6 Ensembl:ENSG00000166173 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:70851655..70851790 26863196 MeRIP-seq:(Medium) rs199816347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462705,Human_RBP_ID_23664254 Human_Splice_Rec_1620454,Human_Splice_Rec_1620456 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96736 RMVar_ID_96736 Human_SNP_ID_582312104 m1A Human chr15 - 70853913 70853913 70853913 GTACCTCAGCCCCGGCTGGGGCAGCGCGAGCGAGGAGGAGCCGAGCCGCGGGCACAGGTAGGCGC GTACCTCAGCCCCGGCTGGGGCAGCGCGAGCGGGGAGGAGCCGAGCCGCGGGCACAGGTAGGCGC T C LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70853876..70854075 32194978 MeRIP-seq:(Medium) rs1039246617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1620445,Human_Splice_Rec_1620455,Human_Splice_Rec_1620457 RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 96737 RMVar_ID_96737 Human_SNP_ID_582312173 m1A Human chr15 + 70854079 70854079 70854079 CGTCTTGGGCCCGGGCCGAGCCTCCCCGCCGGACTGGGCCATGGCTCGCGGGACTGCGGCGCCGC CGTCTTGGGCCCGGGCCGAGCCTCCCCGCCGGGCTGGGCCATGGCTCGCGGGACTGCGGCGCCGC A G LRRC49 Ensembl:ENSG00000137821 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:70853876..70854155 26863410 MeRIP-seq:(Medium) rs1304428684 Functional Loss SNV dbSNP153 33..33 33 - - - 96738 RMVar_ID_96738 Human_SNP_ID_582320969 m1A Human chr15 - 70892130 70892130 70892130 GCGGGGTTGCCGCGCCGACTGGTACGGAGGCAATGACCGCTCGGTCATCTGCTCTGACCACTTTG GCGGGGTTGCCGCGCCGACTGGTACGGAGGCATTGACCGCTCGGTCATCTGCTCTGACCACTTTG T A THAP10 Ensembl:ENSG00000129028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70892085..70892335 32194978 MeRIP-seq:(Medium) rs985856133 Functional Loss SNV dbSNP153 33..33 33 - - - 96739 RMVar_ID_96739 Human_SNP_ID_582320970 m1A Human chr15 - 70892130 70892130 70892130 GCGGGGTTGCCGCGCCGACTGGTACGGAGGCAATGACCGCTCGGTCATCTGCTCTGACCACTTTG GCGGGGTTGCCGCGCCGACTGGTACGGAGGCAGTGACCGCTCGGTCATCTGCTCTGACCACTTTG T C THAP10 Ensembl:ENSG00000129028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70892085..70892335 32194978 MeRIP-seq:(Medium) rs985856133 Functional Loss SNV dbSNP153 33..33 33 - - - 96740 RMVar_ID_96740 Human_SNP_ID_582370031 m1A Human chr15 + 71115531 71115531 71115531 GCGCCTGAACCGCTGGCCGCCCGCGCAGCCCGACGCGGAATCGGGGCACAGCGGGAGCCCGTGCA GCGCCTGAACCGCTGGCCGCCCGCGCAGCCCGGCGCGGAATCGGGGCACAGCGGGAGCCCGTGCA A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:71115485..71115627 26863196 MeRIP-seq:(Medium) rs141040175 Functional Loss SNV dbSNP153 33..33 33 - - - 96741 RMVar_ID_96741 Human_SNP_ID_582370074 m1A Human chr15 + 71115657 71115657 71115657 CCCGGCGCCGGGAACCACGCGGGGGCGAGGCGAGGCGAGGCGGCCGCCGGTCGCTCCGGGACGCG CCCGGCGCCGGGAACCACGCGGGGGCGAGGCGGGGCGAGGCGGCCGCCGGTCGCTCCGGGACGCG A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:71115439..71115666 26863196 MeRIP-seq:(Medium) rs1474139026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1620927 96742 RMVar_ID_96742 Human_SNP_ID_582381117 m1A Human chr15 + 71164749 71164749 71164749 CAGGGGGGTTAAATGCTTTATAGACAAGAAAAAAAAACTGCGCTAGAACCAACTTATTCATCATC CAGGGGGGTTAAATGCTTTATAGACAAGAAAAGAAAACTGCGCTAGAACCAACTTATTCATCATC A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:71164701..71164775 26863196 MeRIP-seq:(Medium) rs1040667450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_122091,RMVar_hsa_circ_309780,RMVar_hsa_circ_371829,RMVar_hsa_circ_126423,RMVar_hsa_circ_283464,RMVar_hsa_circ_122863,RMVar_hsa_circ_98185,RMVar_hsa_circ_106051,RMVar_hsa_circ_115617,RMVar_hsa_circ_102599,RMVar_hsa_circ_92197,RMVar_hsa_circ_95780,RMVar_hsa_circ_90007,RMVar_hsa_circ_173550,RMVar_hsa_circ_173554,RMVar_hsa_circ_173558,RMVar_hsa_circ_82054,RMVar_hsa_circ_173556,RMVar_hsa_circ_173557,RMVar_hsa_circ_173555,RMVar_hsa_circ_173552,RMVar_hsa_circ_173553,RMVar_hsa_circ_173551,RMVar_hsa_circ_173546,RMVar_hsa_circ_173548,RMVar_hsa_circ_173549,RMVar_hsa_circ_173547,RMVar_hsa_circ_173544,RMVar_hsa_circ_173545,RMVar_hsa_circ_104915,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562 96743 RMVar_ID_96743 Human_SNP_ID_582381118 m1A Human chr15 - 71164755 71164754 71164756 GATGATGATGATGAATAAGTTGGTTCTAGCGCAGTTTTTTTTTCTTGTCTATAAAGCATTTAACC GATGATGATGATGAATAAGTTGGTTCTAGCG__GTTTTTTTTTCTTGTCTATAAAGCATTTAACC CTG C THSD4-AS1 Ensembl:ENSG00000259964 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1290126785 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_197607,Human_RBP_ID_886219,Human_RBP_ID_1511846,Human_RBP_ID_2453063,Human_RBP_ID_6457334,Human_RBP_ID_22934669,Human_RBP_ID_24544227,Human_RBP_ID_26326906,Human_RBP_ID_26933935,Human_RBP_ID_27436608,Human_RBP_ID_27809732 96744 RMVar_ID_96744 Human_SNP_ID_582388837 m1A Human chr15 - 71199635 71199635 71199635 CATGCATCACACACACACACCACACACACACCACACACACCACACACCCACACACCACACACACC CATGCATCACACACACACACCACACACACACCCCACACACCACACACCCACACACCACACACACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:71199630..71199901 26863196 MeRIP-seq:(Medium) rs1239824876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2453068 96745 RMVar_ID_96745 Human_SNP_ID_582392788 m1A Human chr15 + 71215330 71215330 71215330 GCCAGCGCTGGCCGGTACGGACGCCAGCCGCCAGGGCCCCACGGTGCTGCGAGGCAGCCGGCACC GCCAGCGCTGGCCGGTACGGACGCCAGCCGCCGGGGCCCCACGGTGCTGCGAGGCAGCCGGCACC A G THSD4 Ensembl:ENSG00000187720 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:71215169..71215412 26863196 MeRIP-seq:(Medium) rs577916799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1620899 RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_122091,RMVar_hsa_circ_309780,RMVar_hsa_circ_371829,RMVar_hsa_circ_126423,RMVar_hsa_circ_283464,RMVar_hsa_circ_122863,RMVar_hsa_circ_98185,RMVar_hsa_circ_106051,RMVar_hsa_circ_115617,RMVar_hsa_circ_102599,RMVar_hsa_circ_92197,RMVar_hsa_circ_95780,RMVar_hsa_circ_90007,RMVar_hsa_circ_173550,RMVar_hsa_circ_173554,RMVar_hsa_circ_173558,RMVar_hsa_circ_82054,RMVar_hsa_circ_173556,RMVar_hsa_circ_173557,RMVar_hsa_circ_173555,RMVar_hsa_circ_173552,RMVar_hsa_circ_173553,RMVar_hsa_circ_173551,RMVar_hsa_circ_173546,RMVar_hsa_circ_173548,RMVar_hsa_circ_173549,RMVar_hsa_circ_173547,RMVar_hsa_circ_173544,RMVar_hsa_circ_173545,RMVar_hsa_circ_104915,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_333937 96746 RMVar_ID_96746 Human_SNP_ID_582392794 m1A Human chr15 + 71215338 71215338 71215338 TGGCCGGTACGGACGCCAGCCGCCAGGGCCCCACGGTGCTGCGAGGCAGCCGGCACCCACAGCCC TGGCCGGTACGGACGCCAGCCGCCAGGGCCCCCCGGTGCTGCGAGGCAGCCGGCACCCACAGCCC A C THSD4 Ensembl:ENSG00000187720 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:71215111..71215438;chr15:71215112..71215454 26863196 MeRIP-seq:(Medium) rs1183727415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1620899 RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_122091,RMVar_hsa_circ_309780,RMVar_hsa_circ_371829,RMVar_hsa_circ_126423,RMVar_hsa_circ_283464,RMVar_hsa_circ_122863,RMVar_hsa_circ_98185,RMVar_hsa_circ_106051,RMVar_hsa_circ_115617,RMVar_hsa_circ_102599,RMVar_hsa_circ_92197,RMVar_hsa_circ_95780,RMVar_hsa_circ_90007,RMVar_hsa_circ_173550,RMVar_hsa_circ_173554,RMVar_hsa_circ_173558,RMVar_hsa_circ_82054,RMVar_hsa_circ_173556,RMVar_hsa_circ_173557,RMVar_hsa_circ_173555,RMVar_hsa_circ_173552,RMVar_hsa_circ_173553,RMVar_hsa_circ_173551,RMVar_hsa_circ_173546,RMVar_hsa_circ_173548,RMVar_hsa_circ_173549,RMVar_hsa_circ_173547,RMVar_hsa_circ_173544,RMVar_hsa_circ_173545,RMVar_hsa_circ_104915,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_333937 96747 RMVar_ID_96747 Human_SNP_ID_582397656 m1A Human chr15 + 71237075 71237075 71237075 TACTGAGGAGGTACAAGTGGTGTGGGTGGTCCATGCAGGGCCAGGGCTGACAAGAGATGCAGCAG TACTGAGGAGGTACAAGTGGTGTGGGTGGTCCGTGCAGGGCCAGGGCTGACAAGAGATGCAGCAG A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:71237067..71237132 26863196 MeRIP-seq:(Medium) rs1206843857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_122091,RMVar_hsa_circ_371829,RMVar_hsa_circ_126423,RMVar_hsa_circ_283464,RMVar_hsa_circ_122863,RMVar_hsa_circ_98185,RMVar_hsa_circ_106051,RMVar_hsa_circ_115617,RMVar_hsa_circ_102599,RMVar_hsa_circ_92197,RMVar_hsa_circ_95780,RMVar_hsa_circ_90007,RMVar_hsa_circ_173550,RMVar_hsa_circ_173554,RMVar_hsa_circ_82054,RMVar_hsa_circ_173556,RMVar_hsa_circ_173557,RMVar_hsa_circ_173555,RMVar_hsa_circ_173552,RMVar_hsa_circ_173553,RMVar_hsa_circ_173551,RMVar_hsa_circ_173546,RMVar_hsa_circ_173548,RMVar_hsa_circ_173549,RMVar_hsa_circ_173547,RMVar_hsa_circ_173544,RMVar_hsa_circ_173545,RMVar_hsa_circ_104915,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_333937 96748 RMVar_ID_96748 Human_SNP_ID_582398983 m1A Human chr15 - 71242624 71242622 71242625 TCCTGCTCCTAAAGAGAGATAGACAAGAGAGGAGATGATCAGAGTCGGATGAATTTCATGTTAAC TCCTGCTCCTAAAGAGAGATAGACAAGAGAG___ATGATCAGAGTCGGATGAATTTCATGTTAAC TCTC T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:71242616..71242771 26863410 MeRIP-seq:(Medium) rs777900586 Functional Loss DEL dbSNP153 32..34 33 - - - 96749 RMVar_ID_96749 Human_SNP_ID_582399042 m1A Human chr15 + 71242762 71242762 71242762 TGCACACACGCCACAGAGGCTCCGGAGACAGAAGCTCTCATCCCGCCATTCCAGGTCCCAGGGAG TGCACACACGCCACAGAGGCTCCGGAGACAGAGGCTCTCATCCCGCCATTCCAGGTCCCAGGGAG A G THSD4 Ensembl:ENSG00000187720 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:71242676..71242763 26863410 MeRIP-seq:(Medium) rs751624116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18436741 RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_122091,RMVar_hsa_circ_371829,RMVar_hsa_circ_126423,RMVar_hsa_circ_283464,RMVar_hsa_circ_122863,RMVar_hsa_circ_98185,RMVar_hsa_circ_106051,RMVar_hsa_circ_115617,RMVar_hsa_circ_102599,RMVar_hsa_circ_92197,RMVar_hsa_circ_95780,RMVar_hsa_circ_90007,RMVar_hsa_circ_173550,RMVar_hsa_circ_173554,RMVar_hsa_circ_82054,RMVar_hsa_circ_173556,RMVar_hsa_circ_173557,RMVar_hsa_circ_173555,RMVar_hsa_circ_173552,RMVar_hsa_circ_173553,RMVar_hsa_circ_173551,RMVar_hsa_circ_173546,RMVar_hsa_circ_173548,RMVar_hsa_circ_173549,RMVar_hsa_circ_173547,RMVar_hsa_circ_173544,RMVar_hsa_circ_173545,RMVar_hsa_circ_104915,RMVar_hsa_circ_64155,RMVar_hsa_circ_100018,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_310563,RMVar_hsa_circ_333937,RMVar_hsa_circ_115334,RMVar_hsa_circ_95482,RMVar_hsa_circ_173564,RMVar_hsa_circ_173565,RMVar_hsa_circ_173566,RMVar_hsa_circ_173563 96750 RMVar_ID_96750 Human_SNP_ID_582550071 m1A Human chr15 - 71825958 71825938 71825959 AAAAACCGTGATTGTTTCCATTAAGCCATCAGAGCGTGTCTCAGATATCTTGTTATACAGTGAAG AAAAACCGTGATTGTTTCCATTAAGCCATCA_____________________TTATACAGTGAAG ACAAGATATCTGAGACACGCTC A MYO9A Ensembl:ENSG00000066933 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:71825830..71826280 32194978 MeRIP-seq:(Medium) rs1364540616 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_462759 96751 RMVar_ID_96751 Human_SNP_ID_582550433 m1A Human chr15 - 71826679 71826679 71826679 AAAAACTCACCTCAGAAAACCAAAGAGACCCCAGAGGGGACAGTCATGTCTGGCCGCAGAAAAAC AAAAACTCACCTCAGAAAACCAAAGAGACCCCGGAGGGGACAGTCATGTCTGGCCGCAGAAAAAC T C MYO9A Ensembl:ENSG00000066933 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:71826628..71826928 32194978 MeRIP-seq:(Medium) rs781412230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27436625 Human_miRNA_ID_934968,Human_miRNA_ID_954843 96752 RMVar_ID_96752 Human_SNP_ID_582551294 m1A Human chr15 - 71830149 71830149 71830149 AACAGCAGCAAGCAGCTATGCAGCAGGAGGAGAGAGTACTGACTGAGCAGATTGAGAACCTACAG AACAGCAGCAAGCAGCTATGCAGCAGGAGGAGTGAGTACTGACTGAGCAGATTGAGAACCTACAG T A MYO9A Ensembl:ENSG00000066933 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:71828016..71830299 32194978 MeRIP-seq:(Medium) rs752211748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1621193,Human_Splice_Rec_1621229,Human_Splice_Rec_1621245,Human_Splice_Rec_1621327,Human_Splice_Rec_1621407,Human_Splice_Rec_1621417 RMVar_hsa_circ_37731,RMVar_hsa_circ_269410,RMVar_hsa_circ_45448,RMVar_hsa_circ_50363,RMVar_hsa_circ_267274 96753 RMVar_ID_96753 Human_SNP_ID_582567256 m1A Human chr15 + 71899904 71899904 71899904 CAAGTACCGCTGCCTCTCTAAGTGAGCACGCCAGGAAGCTTGGAGAAGAGCAGCTGCACTAGCCA CAAGTACCGCTGCCTCTCTAAGTGAGCACGCCGGGAAGCTTGGAGAAGAGCAGCTGCACTAGCCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:71899751..71901235 32194978 MeRIP-seq:(Medium) rs1357962954 Functional Loss SNV dbSNP153 33..33 33 - - - 96754 RMVar_ID_96754 Human_SNP_ID_582621759 m1A Human chr15 + 72118008 72118008 72118008 GTGCAACTACTGCCTCCGCCGCCGCCTCTCGCAGTCCGGGCTGTCCTGTACTCTCTCAACAGACA GTGCAACTACTGCCTCCGCCGCCGCCTCTCGCGGTCCGGGCTGTCCTGTACTCTCTCAACAGACA A G SENP8 Ensembl:ENSG00000166192 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:72117860..72118125 26863196 MeRIP-seq:(Medium) rs4777487 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12736 96755 RMVar_ID_96755 Human_SNP_ID_582640634 m1A Human chr15 + 72199516 72199516 72199516 TGCAAACACAGCCATGTTTCAGTGAGGCGTTGATCTTCTTCCCTGGTGTCCCAACCTACCAGTGC TGCAAACACAGCCATGTTTCAGTGAGGCGTTGTTCTTCTTCCCTGGTGTCCCAACCTACCAGTGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:72199042..72199769 26863196 MeRIP-seq:(Medium) rs1567097131 Functional Loss SNV dbSNP153 33..33 33 - - - 96756 RMVar_ID_96756 Human_SNP_ID_582640635 m1A Human chr15 - 72199519 72199516 72199519 GTGGCACTGGTAGGTTGGGACACCAGGGAAGAAGATCAACGCCTCACTGAAACATGGCTGTGTTT GTGGCACTGGTAGGTTGGGACACCAGGGAAGA___TCAACGCCTCACTGAAACATGGCTGTGTTT ATCT A PKM Ensembl:ENSG00000067225 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:72199468..72199589 26863196 MeRIP-seq:(Medium) rs1567097141 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_41144,Human_RBP_ID_231956,Human_RBP_ID_462817,Human_RBP_ID_758584,Human_RBP_ID_814292,Human_RBP_ID_887134,Human_RBP_ID_1001893,Human_RBP_ID_1279477,Human_RBP_ID_1364026,Human_RBP_ID_1507826,Human_RBP_ID_1833411,Human_RBP_ID_2453241,Human_RBP_ID_3481641,Human_RBP_ID_4347001,Human_RBP_ID_5113044,Human_RBP_ID_6458249,Human_RBP_ID_8421868,Human_RBP_ID_12576876,Human_RBP_ID_17250960,Human_RBP_ID_17366203,Human_RBP_ID_17483607,Human_RBP_ID_18207220,Human_RBP_ID_18281867,Human_RBP_ID_18667374,Human_RBP_ID_20004208,Human_RBP_ID_22496685,Human_RBP_ID_22799169,Human_RBP_ID_23208948,Human_RBP_ID_23307263,Human_RBP_ID_24474488,Human_RBP_ID_26435723,Human_RBP_ID_26934020,Human_RBP_ID_27233677,Human_RBP_ID_27436668 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_101849,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_91473,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173689,RMVar_hsa_circ_173690,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678 96757 RMVar_ID_96757 Human_SNP_ID_582640696 m1A Human chr15 - 72199650 72199650 72199650 ACCAACACCATGCGTGTTGTTCCTGTGCCGTGATGGACCCCAGAGCCCCTCCTCCAGCCCCTGTC ACCAACACCATGCGTGTTGTTCCTGTGCCGTGGTGGACCCCAGAGCCCCTCCTCCAGCCCCTGTC T C PKM Ensembl:ENSG00000067225 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:72199449..72199700;chr15:72199026..72199700;chr15:72199426..72199677 26863196,32194978,32194978 MeRIP-seq:(Medium) rs762479775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462826,Human_RBP_ID_1279478,Human_RBP_ID_1507828,Human_RBP_ID_4347004,Human_RBP_ID_8251094,Human_RBP_ID_8421872,Human_RBP_ID_8801985,Human_RBP_ID_18667379,Human_RBP_ID_22439842,Human_RBP_ID_22532622,Human_RBP_ID_22799170,Human_RBP_ID_23664628,Human_RBP_ID_26934022 Human_miRNA_ID_934971,Human_miRNA_ID_954847,Human_miRNA_ID_2390664,Human_miRNA_ID_2390665,Human_miRNA_ID_2390666,Human_miRNA_ID_2424937,Human_miRNA_ID_2424938,Human_miRNA_ID_2424939,Human_miRNA_ID_2434600,Human_miRNA_ID_2434601,Human_miRNA_ID_2434602,Human_miRNA_ID_2591907,Human_miRNA_ID_2591908,Human_miRNA_ID_2591909,Human_miRNA_ID_3069574,Human_miRNA_ID_3069575,Human_miRNA_ID_3069576 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_101849,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_91473,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173689,RMVar_hsa_circ_173690,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678 96758 RMVar_ID_96758 Human_SNP_ID_582640717 m1A Human chr15 - 72199704 72199704 72199704 AAGAAGGGAGATGTGGTCATTGTGCTGACCGGATGGCGCCCTGGCTCCGGCTTCACCAACACCAT AAGAAGGGAGATGTGGTCATTGTGCTGACCGGTTGGCGCCCTGGCTCCGGCTTCACCAACACCAT T A PKM Ensembl:ENSG00000067225 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:72199615..72199704 26863410 MeRIP-seq:(Medium) rs144132397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41145,Human_RBP_ID_231958,Human_RBP_ID_462827,Human_RBP_ID_885091,Human_RBP_ID_1001895,Human_RBP_ID_1507828,Human_RBP_ID_1833414,Human_RBP_ID_5258727,Human_RBP_ID_6458254,Human_RBP_ID_8421875,Human_RBP_ID_8801987,Human_RBP_ID_12576885,Human_RBP_ID_17250961,Human_RBP_ID_17366205,Human_RBP_ID_17483611,Human_RBP_ID_17651835,Human_RBP_ID_17865869,Human_RBP_ID_18667380,Human_RBP_ID_18982367,Human_RBP_ID_20090900,Human_RBP_ID_22047558,Human_RBP_ID_22439843,Human_RBP_ID_22532623,Human_RBP_ID_22758875,Human_RBP_ID_27155648,Human_RBP_ID_27436675 Human_Splice_Rec_1621760,Human_Splice_Rec_1621776,Human_Splice_Rec_1621792,Human_Splice_Rec_1621806,Human_Splice_Rec_1621820,Human_Splice_Rec_1621836,Human_Splice_Rec_1621844,Human_Splice_Rec_1621846,Human_Splice_Rec_1621862,Human_Splice_Rec_1621880,Human_Splice_Rec_1621896 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_101849,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_91473,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173689,RMVar_hsa_circ_173690,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678 96759 RMVar_ID_96759 Human_SNP_ID_582640953 m1A Human chr15 - 72200590 72200590 72200590 TGCCCCCATCATTGCTGTGACCCGGAATCCCCAGACAGCTCGTCAGGCCCACCTGTACCGTGGCA TGCCCCCATCATTGCTGTGACCCGGAATCCCCCGACAGCTCGTCAGGCCCACCTGTACCGTGGCA T G PKM Ensembl:ENSG00000067225 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72200542..72200925 32194978 MeRIP-seq:(Medium) rs762576055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41146,Human_RBP_ID_462832,Human_RBP_ID_887137,Human_RBP_ID_1279479,Human_RBP_ID_1507833,Human_RBP_ID_1833417,Human_RBP_ID_3481647,Human_RBP_ID_4331830,Human_RBP_ID_6458257,Human_RBP_ID_8421877,Human_RBP_ID_8801989,Human_RBP_ID_12576887,Human_RBP_ID_17250963,Human_RBP_ID_17483612,Human_RBP_ID_17865871,Human_RBP_ID_18667384,Human_RBP_ID_22439846,Human_RBP_ID_22532625,Human_RBP_ID_22759282,Human_RBP_ID_22799172,Human_RBP_ID_26934027,Human_RBP_ID_27155652,Human_RBP_ID_27233682 Human_Splice_Rec_1621758,Human_Splice_Rec_1621774,Human_Splice_Rec_1621790,Human_Splice_Rec_1621804,Human_Splice_Rec_1621818,Human_Splice_Rec_1621834,Human_Splice_Rec_1621842,Human_Splice_Rec_1621860,Human_Splice_Rec_1621878,Human_Splice_Rec_1621894,Human_Splice_Rec_1621910 Human_miRNA_ID_2873703,Human_miRNA_ID_2873704,Human_miRNA_ID_2873705,Human_miRNA_ID_2981666,Human_miRNA_ID_2981667,Human_miRNA_ID_2981668 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_101849,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173689,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 96760 RMVar_ID_96760 Human_SNP_ID_582641045 m1A Human chr15 - 72200957 72200954 72200957 CTGCCTCTCTGTGTCAGAGTTCAGGGTGTAGGAGGGGTTCTGCCAACCATGGGCTGTGTGGGGTA CTGCCTCTCTGTGTCAGAGTTCAGGGTGTAGG___GGTTCTGCCAACCATGGGCTGTGTGGGGTA CCCT C PKM Ensembl:ENSG00000067225 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72200951..72201150 32194978 MeRIP-seq:(Medium) rs1229667214 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_6458269,Human_RBP_ID_9418480,Human_RBP_ID_12576894,Human_RBP_ID_18161644,Human_RBP_ID_21970096,Human_RBP_ID_22579774 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 96761 RMVar_ID_96761 Human_SNP_ID_582641331 m1A Human chr15 - 72202203 72202203 72202203 TCAAAAGCAAATTTATGCTGGAGATTTATTACATAACAGTGCACAGGCTGACTACAAATGGTTAT TCAAAAGCAAATTTATGCTGGAGATTTATTACGTAACAGTGCACAGGCTGACTACAAATGGTTAT T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72202201..72202225 32194978 MeRIP-seq:(Medium) rs1053495677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1507843,Human_RBP_ID_9804414,Human_RBP_ID_12576959 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 96762 RMVar_ID_96762 Human_SNP_ID_582641405 m1A Human chr15 - 72202551 72202551 72202551 AATTATTTGAGGAACTCCGCCGCCTGGCGCCCATTACCAGCGACCCCACAGAAGCCACCGCCGTG AATTATTTGAGGAACTCCGCCGCCTGGCGCCCGTTACCAGCGACCCCACAGAAGCCACCGCCGTG T C PKM Ensembl:ENSG00000067225 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:72202502..72202651;chr15:72202507..72202659 26863196 MeRIP-seq:(Medium) rs1030588233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41153,Human_RBP_ID_462835,Human_RBP_ID_758592,Human_RBP_ID_814297,Human_RBP_ID_887141,Human_RBP_ID_1001901,Human_RBP_ID_1507847,Human_RBP_ID_1833425,Human_RBP_ID_3481656,Human_RBP_ID_4347013,Human_RBP_ID_5180552,Human_RBP_ID_6458307,Human_RBP_ID_8421886,Human_RBP_ID_8801991,Human_RBP_ID_12576969,Human_RBP_ID_17865874,Human_RBP_ID_18667395,Human_RBP_ID_22439848,Human_RBP_ID_22532605,Human_RBP_ID_22759284,Human_RBP_ID_22799180,Human_RBP_ID_22931047,Human_RBP_ID_24474492,Human_RBP_ID_26934042,Human_RBP_ID_27233687,Human_RBP_ID_27436681 Human_Splice_Rec_1621757,Human_Splice_Rec_1621772,Human_Splice_Rec_1621773,Human_Splice_Rec_1621788,Human_Splice_Rec_1621789,Human_Splice_Rec_1621816,Human_Splice_Rec_1621817,Human_Splice_Rec_1621858,Human_Splice_Rec_1621859,Human_Splice_Rec_1621912,Human_Splice_Rec_1621926 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 96763 RMVar_ID_96763 Human_SNP_ID_582641409 m1A Human chr15 + 72202559 72202559 72202559 TGGCTTCTGTGGGGTCGCTGGTAATGGGCGCCAGGCGGCGGAGTTCCTCAAATAATTGCAAGTGG TGGCTTCTGTGGGGTCGCTGGTAATGGGCGCCCGGCGGCGGAGTTCCTCAAATAATTGCAAGTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:72202511..72202663 26863196 MeRIP-seq:(Medium) rs1389054325 Functional Loss SNV dbSNP153 33..33 33 - - - 96764 RMVar_ID_96764 Human_SNP_ID_582641545 m1A Human chr15 - 72203005 72203005 72203005 TGACGGAGTCTGGCAGGTAGGGCCCTAAGGGCAGGTAACACTGTTAGGATAACCAGCCTCTTGCT TGACGGAGTCTGGCAGGTAGGGCCCTAAGGGCGGGTAACACTGTTAGGATAACCAGCCTCTTGCT T C PKM Ensembl:ENSG00000067225 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72203001..72203025 32194978 MeRIP-seq:(Medium) rs1170638398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9804416,Human_RBP_ID_12576986,Human_RBP_ID_20004213 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 96765 RMVar_ID_96765 Human_SNP_ID_582642500 m1A Human chr15 + 72206628 72206628 72206628 GCTGTAACTTGGAGGATAATGAAAGGCTGTGCATAAGAGGATGGAGAAACCTAAAAAGCTCTGCA GCTGTAACTTGGAGGATAATGAAAGGCTGTGCGTAAGAGGATGGAGAAACCTAAAAAGCTCTGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72206626..72206875 32194978 MeRIP-seq:(Medium) rs879521259 Functional Loss SNV dbSNP153 33..33 33 - - - 96766 RMVar_ID_96766 Human_SNP_ID_582642718 m1A Human chr15 + 72207271 72207271 72207271 ACCATGATCCCATCACTGGCCTCCAGGATTTCATCAAACCTGATGGACAAAGTTGGGGGGAGAGA ACCATGATCCCATCACTGGCCTCCAGGATTTCCTCAAACCTGATGGACAAAGTTGGGGGGAGAGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:72207089..72207319;chr15:72207090..72207318 26863196 MeRIP-seq:(Medium) rs753928665 Functional Loss SNV dbSNP153 33..33 33 - - - 96767 RMVar_ID_96767 Human_SNP_ID_582643053 m1A Human chr15 - 72208590 72208590 72208590 AGGCAAGTCCCCGTTGTCCCTGCTCCAGTCCCAGCGCAGCTCTCCGAAGGGCATGGTCCATCCTG AGGCAAGTCCCCGTTGTCCCTGCTCCAGTCCCGGCGCAGCTCTCCGAAGGGCATGGTCCATCCTG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:72208583..72208737 26863410 MeRIP-seq:(Medium) rs1342259341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19067389 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173692,RMVar_hsa_circ_125575,RMVar_hsa_circ_369302,RMVar_hsa_circ_173693,RMVar_hsa_circ_122708,RMVar_hsa_circ_298450,RMVar_hsa_circ_326039,RMVar_hsa_circ_295113,RMVar_hsa_circ_47385,RMVar_hsa_circ_173698,RMVar_hsa_circ_110471,RMVar_hsa_circ_173695,RMVar_hsa_circ_173696,RMVar_hsa_circ_173694,RMVar_hsa_circ_103356,RMVar_hsa_circ_173697 96768 RMVar_ID_96768 Human_SNP_ID_582643464 m1A Human chr15 + 72209626 72209626 72209626 CTTCCCATCTTCCTTGTGTCAAGGAAGTTTAGAGACAAAAGACTGTTTTAGACAACTGGACTCCA CTTCCCATCTTCCTTGTGTCAAGGAAGTTTAGGGACAAAAGACTGTTTTAGACAACTGGACTCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:72209623..72209894 26863196 MeRIP-seq:(Medium) rs1222047335 Functional Loss SNV dbSNP153 33..33 33 - - - 96769 RMVar_ID_96769 Human_SNP_ID_582643686 m1A Human chr15 - 72210303 72210303 72210303 GCGGAGAGCGAGGGGAAGGCTCAGTAGGCAATATGCCCCAGAGACATGTCCTCCAAAGCGCTGGG GCGGAGAGCGAGGGGAAGGCTCAGTAGGCAATGTGCCCCAGAGACATGTCCTCCAAAGCGCTGGG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72210301..72210375 32194978 MeRIP-seq:(Medium) rs1001899736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885741,Human_RBP_ID_19067392,Human_RBP_ID_22355459,Human_RBP_ID_22931099 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,RMVar_hsa_circ_87889,RMVar_hsa_circ_173682,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_369302,RMVar_hsa_circ_173693,RMVar_hsa_circ_122708,RMVar_hsa_circ_326039,RMVar_hsa_circ_295113,RMVar_hsa_circ_47385,RMVar_hsa_circ_173698,RMVar_hsa_circ_110471,RMVar_hsa_circ_173695,RMVar_hsa_circ_173694,RMVar_hsa_circ_103356,RMVar_hsa_circ_307898,RMVar_hsa_circ_173697,RMVar_hsa_circ_327153,RMVar_hsa_circ_291740,RMVar_hsa_circ_173699 96770 RMVar_ID_96770 Human_SNP_ID_582643734 m1A Human chr15 + 72210427 72210427 72210427 CACAGCAACGGGCCGGTAGAGGATGGGGTCAGAAGCAAAGCTTTCCGTGGCTGTGCGCACATTCT CACAGCAACGGGCCGGTAGAGGATGGGGTCAGTAGCAAAGCTTTCCGTGGCTGTGCGCACATTCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72210321..72210430 26863196 MeRIP-seq:(Medium) rs771484755 Functional Loss SNV dbSNP153 33..33 33 - - - 96771 RMVar_ID_96771 Human_SNP_ID_582645412 m1A Human chr15 + 72217482 72217482 72217482 TTCCAGACTTAATCATCTCCTTCAACGTCTCCACTGATCGGGAAGCTGGGCCTATTAGGAAAAGT TTCCAGACTTAATCATCTCCTTCAACGTCTCCGCTGATCGGGAAGCTGGGCCTATTAGGAAAAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:72217356..72217556 26863196 MeRIP-seq:(Medium) rs201533100 Functional Loss SNV dbSNP153 33..33 33 - - - 96772 RMVar_ID_96772 Human_SNP_ID_582648484 m1A Human chr15 + 72229687 72229687 72229687 CTCCCACAGCAGGAAGCTCGTACCCCACTCCCAGCATTACAGGAGATACATTTTAAGATTGTGAG CTCCCACAGCAGGAAGCTCGTACCCCACTCCCCGCATTACAGGAGATACATTTTAAGATTGTGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72229684..72229793 26863196 MeRIP-seq:(Medium) rs1458967987 Functional Loss SNV dbSNP153 33..33 33 - - - 96773 RMVar_ID_96773 Human_SNP_ID_582648780 m1A Human chr15 + 72230490 72230490 72230490 GCGACCAGAGCAGAGAGGGAGGGAGGGAGCGGACACGCCAGGCGAGGAAGGGGATGCGGGGGAGC GCGACCAGAGCAGAGAGGGAGGGAGGGAGCGGGCACGCCAGGCGAGGAAGGGGATGCGGGGGAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:72230486..72230822 26863196 MeRIP-seq:(Medium) rs1215617290 Functional Loss SNV dbSNP153 33..33 33 - - - 96774 RMVar_ID_96774 Human_SNP_ID_582648791 m1A Human chr15 + 72230511 72230511 72230511 GGAGGGAGCGGACACGCCAGGCGAGGAAGGGGATGCGGGGGAGCGGACGTGACCAGCAAGCAGGG GGAGGGAGCGGACACGCCAGGCGAGGAAGGGGGTGCGGGGGAGCGGACGTGACCAGCAAGCAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72230507..72230959 26863196 MeRIP-seq:(Medium) rs563710749 Functional Loss SNV dbSNP153 33..33 33 - - - 96775 RMVar_ID_96775 Human_SNP_ID_582648792 m1A Human chr15 + 72230511 72230511 72230511 GGAGGGAGCGGACACGCCAGGCGAGGAAGGGGATGCGGGGGAGCGGACGTGACCAGCAAGCAGGG GGAGGGAGCGGACACGCCAGGCGAGGAAGGGGTTGCGGGGGAGCGGACGTGACCAGCAAGCAGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72230507..72230959 26863196 MeRIP-seq:(Medium) rs563710749 Functional Loss SNV dbSNP153 33..33 33 - - - 96776 RMVar_ID_96776 Human_SNP_ID_582648989 m1A Human chr15 - 72230999 72230999 72230999 CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCAGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCGGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:72230997..72231225 26863196 MeRIP-seq:(Medium) rs890312 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_12577639 GWAS_ID_12737,GWAS_ID_12738,GWAS_ID_12739,GWAS_ID_12740,GWAS_ID_12741,GWAS_ID_12742,GWAS_ID_12743,GWAS_ID_12744,GWAS_ID_12745,GWAS_ID_12746,GWAS_ID_12747,GWAS_ID_12748,GWAS_ID_12749,GWAS_ID_12750,GWAS_ID_12751,GWAS_ID_12752,GWAS_ID_12753,GWAS_ID_12754,GWAS_ID_12755,GWAS_ID_12756,GWAS_ID_12757 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_127337,RMVar_hsa_circ_173704 96777 RMVar_ID_96777 Human_SNP_ID_582648990 m1A Human chr15 - 72230999 72230999 72230999 CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCAGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCCGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA T G PKM Ensembl:ENSG00000067225 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:72230997..72231225 26863196 MeRIP-seq:(Medium) rs890312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12577639 GWAS_ID_12737,GWAS_ID_12738,GWAS_ID_12739,GWAS_ID_12740,GWAS_ID_12741,GWAS_ID_12742,GWAS_ID_12743,GWAS_ID_12744,GWAS_ID_12745,GWAS_ID_12746,GWAS_ID_12747,GWAS_ID_12748,GWAS_ID_12749,GWAS_ID_12750,GWAS_ID_12751,GWAS_ID_12752,GWAS_ID_12753,GWAS_ID_12754,GWAS_ID_12755,GWAS_ID_12756,GWAS_ID_12757 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_127337,RMVar_hsa_circ_173704 96778 RMVar_ID_96778 Human_SNP_ID_582648998 m1A Human chr15 - 72231020 72231020 72231020 AATCCCGGCGCGCCGGCCGGCCCCGGGCACGCAGGCAGGGCGGCGCAGGATCCAGGGCGTCTGGG AATCCCGGCGCGCCGGCCGGCCCCGGGCACGCGGGCAGGGCGGCGCAGGATCCAGGGCGTCTGGG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr15:72231016..72231250;chr15:72231015..72231225 26863196 MeRIP-seq:(Medium) rs1364717610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_127337,RMVar_hsa_circ_173704 96779 RMVar_ID_96779 Human_SNP_ID_582649061 m1A Human chr15 + 72231165 72231165 72231165 TCGGGCTACGCTGCAAAGACGAAGAGATCCGGAGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC TCGGGCTACGCTGCAAAGACGAAGAGATCCGGCGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:72231022..72231360;chr15:72231025..72231282;chr15:72231038..72231250 26863196 MeRIP-seq:(Medium) rs898013982 Functional Loss SNV dbSNP153 33..33 33 - - - 96780 RMVar_ID_96780 Human_SNP_ID_582649062 m1A Human chr15 + 72231165 72231165 72231165 TCGGGCTACGCTGCAAAGACGAAGAGATCCGGAGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC TCGGGCTACGCTGCAAAGACGAAGAGATCCGGGGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:72231022..72231360;chr15:72231025..72231282;chr15:72231038..72231250 26863196 MeRIP-seq:(Medium) rs898013982 Functional Loss SNV dbSNP153 33..33 33 - - - 96781 RMVar_ID_96781 Human_SNP_ID_582649063 m1A Human chr15 + 72231165 72231165 72231165 TCGGGCTACGCTGCAAAGACGAAGAGATCCGGAGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC TCGGGCTACGCTGCAAAGACGAAGAGATCCGGTGCCACGGCGCGTGCAGCTGCTGTGCAAGGAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:72231022..72231360;chr15:72231025..72231282;chr15:72231038..72231250 26863196 MeRIP-seq:(Medium) rs898013982 Functional Loss SNV dbSNP153 33..33 33 - - - 96782 RMVar_ID_96782 Human_SNP_ID_582651540 m1A Human chr15 - 72241529 72241529 72241529 GCAGATATGAGGATGGTCAGGTGGGCGATGCCAACATTAATACTCAGGACCCCAAGATACAGAAG GCAGATATGAGGATGGTCAGGTGGGCGATGCCGACATTAATACTCAGGACCCCAAGATACAGAAG T C PARP6 Ensembl:ENSG00000137817 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72241480..72241974 32194978 MeRIP-seq:(Medium) rs887113801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1833486,Human_RBP_ID_3945663,Human_RBP_ID_18281876,Human_RBP_ID_18529009,Human_RBP_ID_22935230,Human_RBP_ID_26327706,Human_RBP_ID_27809740 Human_Splice_Rec_1621976,Human_Splice_Rec_1622022,Human_Splice_Rec_1622062,Human_Splice_Rec_1622102,Human_Splice_Rec_1622136,Human_Splice_Rec_1622180,Human_Splice_Rec_1622188,Human_Splice_Rec_1622222,Human_Splice_Rec_1622258,Human_Splice_Rec_1622298,Human_Splice_Rec_1622340,Human_Splice_Rec_1622346,Human_Splice_Rec_1622386,Human_Splice_Rec_1622400,Human_Splice_Rec_1622410 Human_miRNA_ID_1202939 RMVar_hsa_circ_173708 96783 RMVar_ID_96783 Human_SNP_ID_582655957 m1A Human chr15 + 72260584 72260584 72260584 GGTAGCCAAACACTTCCACTTTGGGGTTCTTCATGGTACAGGAGATGGAACGGTTCATGAGGCGC GGTAGCCAAACACTTCCACTTTGGGGTTCTTCGTGGTACAGGAGATGGAACGGTTCATGAGGCGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72260533..72265356 32194978 MeRIP-seq:(Medium) rs1418367005 Functional Loss SNV dbSNP153 33..33 33 - - - 96784 RMVar_ID_96784 Human_SNP_ID_582656466 m1A Human chr15 - 72262639 72262639 72262639 ACAATTATAGTGGTGAAGGTAGGAACCAGAATACAGAAAGTTTGGAGGTGAGTGGTTGGCAACAA ACAATTATAGTGGTGAAGGTAGGAACCAGAATCCAGAAAGTTTGGAGGTGAGTGGTTGGCAACAA T G PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72262613..72262678 26863196 MeRIP-seq:(Medium) rs1461463408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12578031 RMVar_hsa_circ_9426,RMVar_hsa_circ_31452,RMVar_hsa_circ_339985,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479,RMVar_hsa_circ_66016,RMVar_hsa_circ_17062,RMVar_hsa_circ_346708,RMVar_hsa_circ_372081,RMVar_hsa_circ_325960,RMVar_hsa_circ_36613,RMVar_hsa_circ_173713,RMVar_hsa_circ_334421,RMVar_hsa_circ_376788,RMVar_hsa_circ_80437,RMVar_hsa_circ_173715,RMVar_hsa_circ_50652,RMVar_hsa_circ_54380,RMVar_hsa_circ_7425 96785 RMVar_ID_96785 Human_SNP_ID_582658596 m1A Human chr15 - 72271289 72271289 72271289 CTCCCTCTGAAATACCTTTTTCTCCTTGTGATAGCAACAGAAACCAAGCAGCAACAGCCCTTGGA CTCCCTCTGAAATACCTTTTTCTCCTTGTGATGGCAACAGAAACCAAGCAGCAACAGCCCTTGGA T C PARP6,AC009690.3 Ensembl:ENSG00000137817,Ensembl:ENSG00000273025 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72271281..72272575 32194978 MeRIP-seq:(Medium) rs1487343023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41732,Human_RBP_ID_884364,Human_RBP_ID_1507948,Human_RBP_ID_1833528,Human_RBP_ID_19069791,Human_RBP_ID_20054457,Human_RBP_ID_22650085,Human_RBP_ID_25162294 RMVar_hsa_circ_80770,RMVar_hsa_circ_173718 96786 RMVar_ID_96786 Human_SNP_ID_582658902 m1A Human chr15 + 72272420 72272420 72272420 CTCACTTCGTCCACCCCTGCGGAGACGGGGCGAGCCCCGCACCCTTCCCGTGGCCCGGCCGCACC CTCACTTCGTCCACCCCTGCGGAGACGGGGCGGGCCCCGCACCCTTCCCGTGGCCCGGCCGCACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:72272319..72272513 26863196 MeRIP-seq:(Medium) rs1430472121 Functional Loss SNV dbSNP153 33..33 33 - - - 96787 RMVar_ID_96787 Human_SNP_ID_582675677 m1A Human chr15 - 72344013 72344013 72344013 GGTGAATGGTAGTGGAGCCAGGCTTCCACTGCATCCTGGCCAGGGGACGGAGCCCCTTGCCTTCG GGTGAATGGTAGTGGAGCCAGGCTTCCACTGCCTCCTGGCCAGGGGACGGAGCCCCTTGCCTTCG T G HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72343963..72344054 26863196 MeRIP-seq:(Medium) rs1351324583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232851,Human_RBP_ID_462934,Human_RBP_ID_759785,Human_RBP_ID_5113164,Human_RBP_ID_5141417,Human_RBP_ID_5236342,Human_RBP_ID_17651836,Human_RBP_ID_17865925,Human_RBP_ID_18667545,Human_RBP_ID_22440080,Human_RBP_ID_22758881,Human_RBP_ID_23209140 96788 RMVar_ID_96788 Human_SNP_ID_582676405 m1A Human chr15 + 72346599 72346598 72346599 GTCAGGGCCATAGGATATACGGTTCAGGTACCAGGGGGCAGAGAGAAGGGCCCGGAAGCCGGCCT GTCAGGGCCATAGGATATACGGTTCAGGTACC_GGGGGCAGAGAGAAGGGCCCGGAAGCCGGCCT CA C AC009690.2 Ensembl:ENSG00000261460 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72346532..72353772 32194978 MeRIP-seq:(Medium) rs1216659000 Functional Loss DEL dbSNP153 33..33 33 - - - 96789 RMVar_ID_96789 Human_SNP_ID_582683484 m1A Human chr15 + 72375949 72375947 72375949 CGTCCTGCGAACGCTGCCGCCAGCAGCAGCGAAAACCAAAGCCTGGAGCTTGTCATGGCCCGCTG CGTCCTGCGAACGCTGCCGCCAGCAGCAGCG__AACCAAAGCCTGGAGCTTGTCATGGCCCGCTG GAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72375810..72376000 26863196 MeRIP-seq:(Medium) rs1057517348 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_572 96790 RMVar_ID_96790 Human_SNP_ID_582683498 m1A Human chr15 + 72375963 72375963 72375963 TGCCGCCAGCAGCAGCGAAAACCAAAGCCTGGAGCTTGTCATGGCCCGCTGGTCTCCCCTCTCGG TGCCGCCAGCAGCAGCGAAAACCAAAGCCTGGGGCTTGTCATGGCCCGCTGGTCTCCCCTCTCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:72375882..72375967 26863410 MeRIP-seq:(Medium) rs146938346 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_573 96791 RMVar_ID_96791 Human_SNP_ID_582708054 m1A Human chr15 - 72474401 72474401 72474401 CGAGGGGGCCGCTTGCTGCCCGCCTCAGTCAGACGCGGCTCCGCTCCGGCCTCCGAGAGAAAACA CGAGGGGGCCGCTTGCTGCCCGCCTCAGTCAGTCGCGGCTCCGCTCCGGCCTCCGAGAGAAAACA T A TMEM202-AS1 Ensembl:ENSG00000261423 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:72474351..72475000 26863196 MeRIP-seq:(Medium) rs996394202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886371,Human_RBP_ID_5646583 96792 RMVar_ID_96792 Human_SNP_ID_582708090 m1A Human chr15 + 72474470 72474470 72474470 CTCCCTCCCTCCTCCGCGCCCTCCCCGCCGCCACCAGCCGTCAAACGCCAACCGCCGCTCCTGGG CTCCCTCCCTCCTCCGCGCCCTCCCCGCCGCCCCCAGCCGTCAAACGCCAACCGCCGCTCCTGGG A C ARIH1 Ensembl:ENSG00000166233 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:72474370..72474624 26863410 MeRIP-seq:(Medium) rs917255707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9324342,Human_RBP_ID_9371758,Human_RBP_ID_22473426 96793 RMVar_ID_96793 Human_SNP_ID_582710368 m1A Human chr15 + 72482458 72482458 72482458 GTTGTCAAAGATGGCTAGGATTTGGGTGGATAAAAAAGAGGAAGTCATTCTAAGGAACTGAATGA GTTGTCAAAGATGGCTAGGATTTGGGTGGATAGAAAAGAGGAAGTCATTCTAAGGAACTGAATGA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72482456..72482578 26863196 MeRIP-seq:(Medium) rs1169655838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6459017,Human_RBP_ID_12579728 96794 RMVar_ID_96794 Human_SNP_ID_582768968 m1A Human chr15 + 72736808 72736808 72736808 TCAGAAGTTGGGAGCTGCTCTCCAGGTTGGGGAGGCACTGGTCTGGACCAAACCAGTTAAAGATC TCAGAAGTTGGGAGCTGCTCTCCAGGTTGGGGGGGCACTGGTCTGGACCAAACCAGTTAAAGATC A G BBS4 Ensembl:ENSG00000140463 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72736751..72736850 32194978 MeRIP-seq:(Medium) rs774171182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6460789,Human_RBP_ID_17870204,Human_RBP_ID_22496720 Human_Splice_Rec_1623114,Human_Splice_Rec_1623142,Human_Splice_Rec_1623250,Human_Splice_Rec_1623280,Human_Splice_Rec_1623310,Human_Splice_Rec_1623372,Human_Splice_Rec_1623376 RMVar_hsa_circ_162 96795 RMVar_ID_96795 Human_SNP_ID_582768969 m1A Human chr15 + 72736808 72736808 72736808 TCAGAAGTTGGGAGCTGCTCTCCAGGTTGGGGAGGCACTGGTCTGGACCAAACCAGTTAAAGATC TCAGAAGTTGGGAGCTGCTCTCCAGGTTGGGGTGGCACTGGTCTGGACCAAACCAGTTAAAGATC A T BBS4 Ensembl:ENSG00000140463 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:72736751..72736850 32194978 MeRIP-seq:(Medium) rs774171182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6460789,Human_RBP_ID_17870204,Human_RBP_ID_22496720 Human_Splice_Rec_1623114,Human_Splice_Rec_1623142,Human_Splice_Rec_1623250,Human_Splice_Rec_1623280,Human_Splice_Rec_1623310,Human_Splice_Rec_1623372,Human_Splice_Rec_1623376 RMVar_hsa_circ_162 96796 RMVar_ID_96796 Human_SNP_ID_582780307 m1A Human chr15 + 72783478 72783478 72783478 CGTTGGCACTCACCCCACTGCCACGCGGCGCCAGCGCCGGACTGGCCGCACGATAAGCGCGTCCC CGTTGGCACTCACCCCACTGCCACGCGGCGCCGGCGCCGGACTGGCCGCACGATAAGCGCGTCCC A G ADPGK-AS1 Ensembl:ENSG00000260898 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72783451..72783681 32194978 MeRIP-seq:(Medium) rs1307590095 Functional Loss SNV dbSNP153 33..33 33 - - - 96797 RMVar_ID_96797 Human_SNP_ID_582780373 m1A Human chr15 + 72783604 72783604 72783604 ACACAGCGAGCTCCAGAGAGAGCGCAGCGCCGAGCCTGGCAGCTCTGGCTCCAGCAGGAAGACGC ACACAGCGAGCTCCAGAGAGAGCGCAGCGCCGGGCCTGGCAGCTCTGGCTCCAGCAGGAAGACGC A G ADPGK-AS1 Ensembl:ENSG00000260898 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72783553..72783703 26863196 MeRIP-seq:(Medium) rs1266259117 Functional Loss SNV dbSNP153 33..33 33 - - - 96798 RMVar_ID_96798 Human_SNP_ID_582842124 m1A Human chr15 - 73052553 73052543 73052553 GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCAGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCC__________GGCCCGGCCCGGCCCGCGCAGCC CGGGCTGGGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73052502..73052739 26863196 MeRIP-seq:(Medium) rs1040486027 Functional Loss DEL dbSNP153 33..42 33 - - - 96799 RMVar_ID_96799 Human_SNP_ID_582842125 m1A Human chr15 - 73052553 73052543 73052553 GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCAGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCC_____AGCCCGGCCCGGCCCGGCCCGCGCAGCC CGGGCTGGGCT CGGGCT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73052502..73052739 26863196 MeRIP-seq:(Medium) rs1040486027 Functional Loss DEL dbSNP153 33..37 33 - - - 96800 RMVar_ID_96800 Human_SNP_ID_582842130 m1A Human chr15 - 73052553 73052553 73052553 GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCAGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCGGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73052502..73052739 26863196 MeRIP-seq:(Medium) rs1175120345 Functional Loss SNV dbSNP153 33..33 33 - - - 96801 RMVar_ID_96801 Human_SNP_ID_582842131 m1A Human chr15 - 73052553 73052553 73052553 GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCAGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC GCAAGCTCGGCTCCCGCGGCCGCCGCTGCTCCCGCCCAGCCCGGCCCGGCCCGGCCCGCGCAGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73052502..73052739 26863196 MeRIP-seq:(Medium) rs1175120345 Functional Loss SNV dbSNP153 33..33 33 - - - 96802 RMVar_ID_96802 Human_SNP_ID_582900265 m1A Human chr15 + 73298545 73298545 73298545 CCCACCCATTGAAGAGCTTCGCCGTGCCAGCAATCCCGCCTCCAGGACCTCCCACCTATGATCCT CCCACCCATTGAAGAGCTTCGCCGTGCCAGCAGTCCCGCCTCCAGGACCTCCCACCTATGATCCT A G NEO1 Ensembl:ENSG00000067141 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73298498..73298609 26863196 MeRIP-seq:(Medium) rs762952907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17252426 Human_Splice_Rec_1623529,Human_Splice_Rec_1623585,Human_Splice_Rec_1623639,Human_Splice_Rec_1623693,Human_Splice_Rec_1623741,Human_Splice_Rec_1623763,Human_Splice_Rec_1623767 RMVar_hsa_circ_7018,RMVar_hsa_circ_69656,RMVar_hsa_circ_42332 96803 RMVar_ID_96803 Human_SNP_ID_582971523 m1A Human chr15 - 73592105 73592105 73592105 AGCCAAGGATTGTCACCAGTGAAGAGGTCATTATTCGAGACAGCCCTGTTCTCCCTGTCACCCTG AGCCAAGGATTGTCACCAGTGAAGAGGTCATTTTTCGAGACAGCCCTGTTCTCCCTGTCACCCTG T A NPTN Ensembl:ENSG00000156642 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:73592004..73592105 32194978 MeRIP-seq:(Medium) rs750139690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1508253,Human_RBP_ID_4332595,Human_RBP_ID_8422406,Human_RBP_ID_12586790 Human_Splice_Rec_1623812,Human_Splice_Rec_1623826,Human_Splice_Rec_1623850,Human_Splice_Rec_1623870,Human_Splice_Rec_1623886,Human_Splice_Rec_1623902,Human_Splice_Rec_1623906 RMVar_hsa_circ_346902,RMVar_hsa_circ_29713,RMVar_hsa_circ_310352,RMVar_hsa_circ_173831,RMVar_hsa_circ_173832,RMVar_hsa_circ_332967,RMVar_hsa_circ_340804,RMVar_hsa_circ_34760 96804 RMVar_ID_96804 Human_SNP_ID_582971526 m1A Human chr15 + 73592110 73592110 73592110 TGACAGGGAGAACAGGGCTGTCTCGAATAATGACCTCTTCACTGGTGACAATCCTTGGCTCTGTA TGACAGGGAGAACAGGGCTGTCTCGAATAATGCCCTCTTCACTGGTGACAATCCTTGGCTCTGTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73592059..73592178 26863196 MeRIP-seq:(Medium) rs766221405 Functional Loss SNV dbSNP153 33..33 33 - - - 96805 RMVar_ID_96805 Human_SNP_ID_582971531 m1A Human chr15 - 73592123 73592123 73592123 TGTGCACTCTTATTACAGAGCCAAGGATTGTCACCAGTGAAGAGGTCATTATTCGAGACAGCCCT TGTGCACTCTTATTACAGAGCCAAGGATTGTCGCCAGTGAAGAGGTCATTATTCGAGACAGCCCT T C NPTN Ensembl:ENSG00000156642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:73592072..73592199 26863196 MeRIP-seq:(Medium) rs1318907347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1508254,Human_RBP_ID_4343258,Human_RBP_ID_8422406,Human_RBP_ID_12586790,Human_RBP_ID_22496737,Human_RBP_ID_23665836,Human_RBP_ID_26634196 Human_Splice_Rec_1623812,Human_Splice_Rec_1623826,Human_Splice_Rec_1623850,Human_Splice_Rec_1623870,Human_Splice_Rec_1623886,Human_Splice_Rec_1623902,Human_Splice_Rec_1623906 RMVar_hsa_circ_346902,RMVar_hsa_circ_29713,RMVar_hsa_circ_310352,RMVar_hsa_circ_173831,RMVar_hsa_circ_173832,RMVar_hsa_circ_332967,RMVar_hsa_circ_340804,RMVar_hsa_circ_34760 96806 RMVar_ID_96806 Human_SNP_ID_582993206 m1A Human chr15 - 73684809 73684809 73684809 GCCCGCTCCAGACCCGGGGCCTGCAAAAGCGCATTCACCCACCCGGCCCGGTCCGCAGCTTCCGG GCCCGCTCCAGACCCGGGGCCTGCAAAAGCGCGTTCACCCACCCGGCCCGGTCCGCAGCTTCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73684802..73685094 26863196 MeRIP-seq:(Medium) rs563642131 Functional Loss SNV dbSNP153 33..33 33 - - - 96807 RMVar_ID_96807 Human_SNP_ID_582994624 m1A Human chr15 + 73691027 73691027 73691027 TTCTGGCTGTTGTATAGAGTATAGATTGGAGAACAGAATTGGGTGGGGGAACTAGAGAAGGTGAA TTCTGGCTGTTGTATAGAGTATAGATTGGAGAGCAGAATTGGGTGGGGGAACTAGAGAAGGTGAA A G CD276 Ensembl:ENSG00000103855 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:73691021..73691170 26863196 MeRIP-seq:(Medium) rs905124167 Functional Loss SNV dbSNP153 33..33 33 - - - 96808 RMVar_ID_96808 Human_SNP_ID_582994638 m1A Human chr15 + 73691103 73691103 73691103 AGAGGCTTTTATAGTTATCCAGGCAAGAGATGATGGTGACTTGGAAGACCAGGAAGAGAAGCAGG AGAGGCTTTTATAGTTATCCAGGCAAGAGATGGTGGTGACTTGGAAGACCAGGAAGAGAAGCAGG A G CD276 Ensembl:ENSG00000103855 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73691101..73691169 26863196 MeRIP-seq:(Medium) rs1021514220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12588148 96809 RMVar_ID_96809 Human_SNP_ID_582997270 m1A Human chr15 - 73702410 73702410 73702410 ATAGGCGCTGCCCTGGTCCTGGCCCTCAGCAAAGCTGTGCACCAGCTGTTTGGTATCTGTCAGCT ATAGGCGCTGCCCTGGTCCTGGCCCTCAGCAACGCTGTGCACCAGCTGTTTGGTATCTGTCAGCT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73699598..73702535 32194978 MeRIP-seq:(Medium) rs932883539 Functional Loss SNV dbSNP153 33..33 33 - - - 96810 RMVar_ID_96810 Human_SNP_ID_583000332 m1A Human chr15 - 73713070 73713070 73713070 AGTGGTCTGTGTATCGCATCCTTTGGAGAAGGAGCCCACCTGTCAGAGCAGGATGCATCTGTTGG AGTGGTCTGTGTATCGCATCCTTTGGAGAAGGTGCCCACCTGTCAGAGCAGGATGCATCTGTTGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73713019..73713120 32194978 MeRIP-seq:(Medium) rs1391293505 Functional Loss SNV dbSNP153 33..33 33 - - - 96811 RMVar_ID_96811 Human_SNP_ID_583000483 m1A Human chr15 - 73713667 73713667 73713667 GGGCACTGCAGAGGAGGCTGGGCCAGGGGGGAACCACACGTGTTCCAGCACGTGCACCTGCAGGT GGGCACTGCAGAGGAGGCTGGGCCAGGGGGGAGCCACACGTGTTCCAGCACGTGCACCTGCAGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73713617..73713692 26863196 MeRIP-seq:(Medium) rs756364362 Functional Loss SNV dbSNP153 33..33 33 - - - 96812 RMVar_ID_96812 Human_SNP_ID_583000484 m1A Human chr15 - 73713667 73713667 73713667 GGGCACTGCAGAGGAGGCTGGGCCAGGGGGGAACCACACGTGTTCCAGCACGTGCACCTGCAGGT GGGCACTGCAGAGGAGGCTGGGCCAGGGGGGACCCACACGTGTTCCAGCACGTGCACCTGCAGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:73713617..73713692 26863196 MeRIP-seq:(Medium) rs756364362 Functional Loss SNV dbSNP153 33..33 33 - - - 96813 RMVar_ID_96813 Human_SNP_ID_583056178 m1A Human chr15 - 73926609 73926609 73926609 AGCGGGACGGCTCCTCCGATGACAGCATTTCAAGGCCAAGGGGTCAGGGCAGGGCAGGGGCGGTG AGCGGGACGGCTCCTCCGATGACAGCATTTCACGGCCAAGGGGTCAGGGCAGGGCAGGGGCGGTG T G LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:73926515..73926626 26863196 MeRIP-seq:(Medium) rs1441233710 Functional Loss SNV dbSNP153 33..33 33 - - - 96814 RMVar_ID_96814 Human_SNP_ID_583056270 m1A Human chr15 + 73926887 73926887 73926887 CGGGCAGCAGGCGCAGCCCGGGCAGGGCTCGGACCCCGCCCGCTGGCGGCAGCTGATCCAGTGGG CGGGCAGCAGGCGCAGCCCGGGCAGGGCTCGGCCCCCGCCCGCTGGCGGCAGCTGATCCAGTGGG A C LOXL1 Ensembl:ENSG00000129038 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73926885..73927234 32194978 MeRIP-seq:(Medium) rs1485526480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102253,RMVar_hsa_circ_173838 96815 RMVar_ID_96815 Human_SNP_ID_583056446 m1A Human chr15 - 73927337 73927316 73927337 GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGACGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC GCGACGCGGGGTCGTAGTTCTCGTACTGGCTG_____________________GGGAACTGCTGC CCTACCCGCAGGCGCCCTTCGT C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927333..73927483 32194978 MeRIP-seq:(Medium) rs1555432577 Functional Loss DEL dbSNP153 33..53 33 - - - 96816 RMVar_ID_96816 Human_SNP_ID_583056447 m1A Human chr15 - 73927337 73927317 73927337 GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGACGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC GCGACGCGGGGTCGTAGTTCTCGTACTGGCTG____________________GGGGAACTGCTGC CTACCCGCAGGCGCCCTTCGT C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927333..73927483 32194978 MeRIP-seq:(Medium) rs1555432579 Functional Loss DEL dbSNP153 33..52 33 - - - 96817 RMVar_ID_96817 Human_SNP_ID_583056453 m1A Human chr15 - 73927337 73927324 73927337 GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGACGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC GCGACGCGGGGTCGTAGTTCTCGTACTGGCTG_____________GCGGGTAGGGGAACTGCTGC CAGGCGCCCTTCGT C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927333..73927483 32194978 MeRIP-seq:(Medium) rs1555432591 Functional Loss DEL dbSNP153 33..45 33 - - - 96818 RMVar_ID_96818 Human_SNP_ID_583056460 m1A Human chr15 - 73927337 73927332 73927337 GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGACGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC GCGACGCGGGGTCGTAGTTCTCGTACTGGCTG_____GGGCGCCTGCGGGTAGGGGAACTGCTGC CTTCGT C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927333..73927483 32194978 MeRIP-seq:(Medium) rs1555432594 Functional Loss DEL dbSNP153 33..37 33 - - - 96819 RMVar_ID_96819 Human_SNP_ID_583056465 m1A Human chr15 - 73927337 73927337 73927337 GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGACGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC GCGACGCGGGGTCGTAGTTCTCGTACTGGCTGGCGAAGGGCGCCTGCGGGTAGGGGAACTGCTGC T C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927333..73927483 32194978 MeRIP-seq:(Medium) rs201802712 Functional Loss SNV dbSNP153 33..33 33 - - - 96820 RMVar_ID_96820 Human_SNP_ID_583056712 m1A Human chr15 - 73927859 73927859 73927859 ACTCACCGCGGCCGTTCTGGTTGGGCCGGTACACGCTGCCCACGCTGAGGCGGCCCTGCTGCGCG ACTCACCGCGGCCGTTCTGGTTGGGCCGGTACGCGCTGCCCACGCTGAGGCGGCCCTGCTGCGCG T C LOXL1-AS1 Ensembl:ENSG00000261801 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73927731..73941921 32194978 MeRIP-seq:(Medium) rs905975149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4332889 Human_Splice_Rec_1624169,Human_Splice_Rec_1624195,Human_Splice_Rec_1624203,Human_Splice_Rec_1624209 96821 RMVar_ID_96821 Human_SNP_ID_583071131 m1A Human chr15 - 73983447 73983447 73983447 TGGCGAAGTTACCTGGGGATCCTGGCTGGCCCACCTTCCTGGCTGCAGTCCAGGCCCGTGCTGGC TGGCGAAGTTACCTGGGGATCCTGGCTGGCCCGCCTTCCTGGCTGCAGTCCAGGCCCGTGCTGGC T C STOML1 Ensembl:ENSG00000067221 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2289411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437717 96822 RMVar_ID_96822 Human_SNP_ID_583073296 m1A Human chr15 + 73992189 73992189 73992189 AGCTCGACTGCTGGAAGCGGTCAAAATCACCCAGGGGCAGCGCCCGGTACCCAGACCTGCCGAGC AGCTCGACTGCTGGAAGCGGTCAAAATCACCCGGGGGCAGCGCCCGGTACCCAGACCTGCCGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73992139..73992287 26863196 MeRIP-seq:(Medium) rs916404296 Functional Loss SNV dbSNP153 33..33 33 - - - 96823 RMVar_ID_96823 Human_SNP_ID_583073297 m1A Human chr15 + 73992189 73992189 73992189 AGCTCGACTGCTGGAAGCGGTCAAAATCACCCAGGGGCAGCGCCCGGTACCCAGACCTGCCGAGC AGCTCGACTGCTGGAAGCGGTCAAAATCACCCTGGGGCAGCGCCCGGTACCCAGACCTGCCGAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73992139..73992287 26863196 MeRIP-seq:(Medium) rs916404296 Functional Loss SNV dbSNP153 33..33 33 - - - 96824 RMVar_ID_96824 Human_SNP_ID_583073941 m1A Human chr15 - 73994821 73994821 73994821 TCCTGCTGGGGCCTCGGAGATCGGGCGGGTGCAGGCTCCATGGACCCCAGCTTAGTTTCGATTCT TCCTGCTGGGGCCTCGGAGATCGGGCGGGTGCGGGCTCCATGGACCCCAGCTTAGTTTCGATTCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr15:73994726..73994984;chr15:73994720..73995016 26863196 MeRIP-seq:(Medium) rs943351047 Functional Loss SNV dbSNP153 33..33 33 - - - 96825 RMVar_ID_96825 Human_SNP_ID_583080263 m1A Human chr15 - 74023138 74023138 74023138 CCGACTGGCCATCTCCTCGTAGTCGCGCTGGTACCGCGCGTCCACAGCCTCCAGCAGCTCGCGCT CCGACTGGCCATCTCCTCGTAGTCGCGCTGGTGCCGCGCGTCCACAGCCTCCAGCAGCTCGCGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74023087..74023169 26863196 MeRIP-seq:(Medium) rs538982599 Functional Loss SNV dbSNP153 33..33 33 - - - 96826 RMVar_ID_96826 Human_SNP_ID_583083134 m1A Human chr15 + 74035451 74035451 74035451 GTGGGATCCGCTACCTGTTGTACAGAGCACAGAGAGCCATCCGCCTTCGCCATGCCCTCCGCTTG GTGGGATCCGCTACCTGTTGTACAGAGCACAGGGAGCCATCCGCCTTCGCCATGCCCTCCGCTTG A G PML Ensembl:ENSG00000140464 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:74035400..74035516 26863196 MeRIP-seq:(Medium) rs1457140433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463395,Human_RBP_ID_21888338 RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 96827 RMVar_ID_96827 Human_SNP_ID_583083397 m1A Human chr15 - 74036003 74036003 74036003 CCTGTAAGAGCATGGGCTGGAGGAGGCAGCTCAGGGGCCGGGCAGGGGTGTTGGCTGCAAGGTTA CCTGTAAGAGCATGGGCTGGAGGAGGCAGCTCGGGGGCCGGGCAGGGGTGTTGGCTGCAAGGTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74035897..74036009 26863196 MeRIP-seq:(Medium) rs1223963568 Functional Loss SNV dbSNP153 33..33 33 - - - 96828 RMVar_ID_96828 Human_SNP_ID_583083469 m1A Human chr15 + 74036235 74036235 74036235 AAGAAACTTCTGTCACCCTTGCACTCTCCTGTATTCTGAGTCCCTGGCCAATAGCACAGCCTTCC AAGAAACTTCTGTCACCCTTGCACTCTCCTGTGTTCTGAGTCCCTGGCCAATAGCACAGCCTTCC A G PML Ensembl:ENSG00000140464 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12588274,Human_RBP_ID_17077044,Human_RBP_ID_18938326,Human_RBP_ID_26435877 GWAS_ID_12758,GWAS_ID_12759,GWAS_ID_12760,GWAS_ID_12761,GWAS_ID_12762,GWAS_ID_12763,GWAS_ID_12764,GWAS_ID_12765,GWAS_ID_12766,GWAS_ID_12767,GWAS_ID_12768,GWAS_ID_12769,GWAS_ID_12770,GWAS_ID_12771,GWAS_ID_12772,GWAS_ID_12773,GWAS_ID_12774 RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 96829 RMVar_ID_96829 Human_SNP_ID_583123821 m1A Human chr15 + 74203065 74203065 74203065 AGCCCCTGCCCGCCACATCTGCAGTGCCGCACACAGACAGGAGACCAGCATTACAGCAACAACCG AGCCCCTGCCCGCCACATCTGCAGTGCCGCACGCAGACAGGAGACCAGCATTACAGCAACAACCG A G CCDC33 Ensembl:ENSG00000140481 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74202989..74203104 26863196 MeRIP-seq:(Medium) rs1019073358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1625177,Human_Splice_Rec_1625185,Human_Splice_Rec_1625191 96830 RMVar_ID_96830 Human_SNP_ID_583162061 m1A Human chr15 - 74359215 74359215 74359215 GGAACCTAGAGTGGGAGAGATTAAGCCAAAGGAAGATTTTGTGGTAAGGGGTGATATTGTGGGGT GGAACCTAGAGTGGGAGAGATTAAGCCAAAGGGAGATTTTGTGGTAAGGGGTGATATTGTGGGGT T C CYP11A1 Ensembl:ENSG00000140459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:74359152..74359235 26863196 MeRIP-seq:(Medium) rs1352804961 Functional Loss SNV dbSNP153 33..33 33 - - - 96831 RMVar_ID_96831 Human_SNP_ID_583174153 m1A Human chr15 + 74409761 74409761 74409761 CCGTTTCCCTCACCCCACCCCCTCCCATAACCACCCCCAACACTAGGGGCTCCAACAACGTCCCC CCGTTTCCCTCACCCCACCCCCTCCCATAACCCCCCCCAACACTAGGGGCTCCAACAACGTCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74409710..74409891 26863196 MeRIP-seq:(Medium) rs1481070852 Functional Loss SNV dbSNP153 33..33 33 - - - 96832 RMVar_ID_96832 Human_SNP_ID_583174154 m1A Human chr15 + 74409761 74409761 74409761 CCGTTTCCCTCACCCCACCCCCTCCCATAACCACCCCCAACACTAGGGGCTCCAACAACGTCCCC CCGTTTCCCTCACCCCACCCCCTCCCATAACCTCCCCCAACACTAGGGGCTCCAACAACGTCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74409710..74409891 26863196 MeRIP-seq:(Medium) rs1481070852 Functional Loss SNV dbSNP153 33..33 33 - - - 96833 RMVar_ID_96833 Human_SNP_ID_583180686 m1A Human chr15 + 74433862 74433853 74433862 CGCAGCGGAAGCCCCAACCGAGCCGGCGGGCCAGGGACGCGGGCGCGCGGTGCGCTGGGGGCGGC CGCAGCGGAAGCCCCAACCGAGCC_________GGGACGCGGGCGCGCGGTGCGCTGGGGGCGGC CGGCGGGCCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74433812..74433931 26863196 MeRIP-seq:(Medium) rs964003025 Functional Loss DEL dbSNP153 25..33 33 - - - 96834 RMVar_ID_96834 Human_SNP_ID_583183498 m1A Human chr15 + 74446154 74446154 74446154 GGGCTGCTTGGATGTCCCCACCGGTGGCCTGCAGGGCCCGCAGGCTCAGCTCATCGTCCTGGATG GGGCTGCTTGGATGTCCCCACCGGTGGCCTGCGGGGCCCGCAGGCTCAGCTCATCGTCCTGGATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74446105..74448574 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96835 RMVar_ID_96835 Human_SNP_ID_583186521 m1A Human chr15 - 74458890 74458887 74458891 ACCACTGAGGTTTTGTTCTTTTACAGGGAGAAAGAGAGAGCGCGAAAGAGAGAGGATGTCTCTCT ACCACTGAGGTTTTGTTCTTTTACAGGGAGA____GAGAGCGCGAAAGAGAGAGGATGTCTCTCT CTCTT C UBL7 Ensembl:ENSG00000138629 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74458801..74458959 26863196 MeRIP-seq:(Medium) rs748817139 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_4342810 Human_Splice_Rec_1625506,Human_Splice_Rec_1625528,Human_Splice_Rec_1625548,Human_Splice_Rec_1625568,Human_Splice_Rec_1625590,Human_Splice_Rec_1625610,Human_Splice_Rec_1625622 RMVar_hsa_circ_118626,RMVar_hsa_circ_104535,RMVar_hsa_circ_173860,RMVar_hsa_circ_173859,RMVar_hsa_circ_109251,RMVar_hsa_circ_173861 96836 RMVar_ID_96836 Human_SNP_ID_583187118 m1A Human chr15 + 74460993 74460993 74460993 GACTCAGTAAAATCACTGGCCCAAGGTCACAGATCGCTAGTAATGGGGCAGGAACACTATCCGGT GACTCAGTAAAATCACTGGCCCAAGGTCACAGGTCGCTAGTAATGGGGCAGGAACACTATCCGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74460991..74461175 26863196 MeRIP-seq:(Medium) rs994493552 Functional Loss SNV dbSNP153 33..33 33 - - - 96837 RMVar_ID_96837 Human_SNP_ID_583187132 m1A Human chr15 - 74461045 74461045 74461045 GCTCGATGTGTGTCAGCCAAGTAGCTGGTCCCACTGGAGCGGTGAGGTCGCCACCGGATAGTGTT GCTCGATGTGTGTCAGCCAAGTAGCTGGTCCCCCTGGAGCGGTGAGGTCGCCACCGGATAGTGTT T G UBL7 Ensembl:ENSG00000138629 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:74461036..74461127 26863410 MeRIP-seq:(Medium) rs986918087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342389 Human_Splice_Rec_1625547,Human_Splice_Rec_1625587,Human_Splice_Rec_1625609,Human_Splice_Rec_1625621 RMVar_hsa_circ_118626,RMVar_hsa_circ_173860 96838 RMVar_ID_96838 Human_SNP_ID_583187142 m1A Human chr15 - 74461084 74461084 74461084 GCGGGACGGGTGAGGGCGCTGGGGCCCTGGGCAGCGCGGGCTCGATGTGTGTCAGCCAAGTAGCT GCGGGACGGGTGAGGGCGCTGGGGCCCTGGGCGGCGCGGGCTCGATGTGTGTCAGCCAAGTAGCT T C UBL7 Ensembl:ENSG00000138629 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:74461006..74461132 26863196 MeRIP-seq:(Medium) rs35032603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758948,Human_RBP_ID_815553,Human_RBP_ID_4333074,Human_RBP_ID_18418393,Human_RBP_ID_23666211 Human_Splice_Rec_1625547,Human_Splice_Rec_1625587,Human_Splice_Rec_1625609,Human_Splice_Rec_1625621 RMVar_hsa_circ_118626,RMVar_hsa_circ_173860 96839 RMVar_ID_96839 Human_SNP_ID_583187144 m1A Human chr15 + 74461089 74461089 74461089 CTTGGCTGACACACATCGAGCCCGCGCTGCCCAGGGCCCCAGCGCCCTCACCCGTCCCGCGGAAG CTTGGCTGACACACATCGAGCCCGCGCTGCCCCGGGCCCCAGCGCCCTCACCCGTCCCGCGGAAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74461003..74461175 26863196 MeRIP-seq:(Medium) rs1353381815 Functional Loss SNV dbSNP153 33..33 33 - - - 96840 RMVar_ID_96840 Human_SNP_ID_583220582 m1A Human chr15 + 74598648 74598648 74598648 GAAGAAAGCAAGCAGGAGTGGCGCGAACAGGAAGGGACTAGGGATAGAAGCCGGGCTTGGACACA GAAGAAAGCAAGCAGGAGTGGCGCGAACAGGAGGGGACTAGGGATAGAAGCCGGGCTTGGACACA A G CLK3 Ensembl:ENSG00000179335 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74598617..74598810 26863196 MeRIP-seq:(Medium) rs1274719377 Functional Loss SNV dbSNP153 33..33 33 - - - 96841 RMVar_ID_96841 Human_SNP_ID_583225607 m1A Human chr15 + 74619260 74619260 74619260 AACCAGACCCGTACCTGAGCTACCGATGGAAGAGGAGGAGGTCCTACAGTCGGGAACATGAAGGG AACCAGACCCGTACCTGAGCTACCGATGGAAGGGGAGGAGGTCCTACAGTCGGGAACATGAAGGG A G CLK3 Ensembl:ENSG00000179335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74619176..74619356 26863196 MeRIP-seq:(Medium) rs1037371577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885772,Human_RBP_ID_1834013,Human_RBP_ID_9371137,Human_RBP_ID_26326925 Human_Splice_Rec_1625750,Human_Splice_Rec_1625751,Human_Splice_Rec_1625774,Human_Splice_Rec_1625775,Human_Splice_Rec_1625796,Human_Splice_Rec_1625797,Human_Splice_Rec_1625800,Human_Splice_Rec_1625801,Human_Splice_Rec_1625824,Human_Splice_Rec_1625825,Human_Splice_Rec_1625846,Human_Splice_Rec_1625847,Human_Splice_Rec_1625858,Human_Splice_Rec_1625859,Human_Splice_Rec_1625878,Human_Splice_Rec_1625879,Human_Splice_Rec_1625884,Human_Splice_Rec_1625885,Human_Splice_Rec_1625894,Human_Splice_Rec_1625895,Human_Splice_Rec_1625906,Human_Splice_Rec_1625907,Human_Splice_Rec_1625909,Human_Splice_Rec_1625913 RMVar_hsa_circ_11090,RMVar_hsa_circ_320709,RMVar_hsa_circ_361241,RMVar_hsa_circ_370113,RMVar_hsa_circ_346961,RMVar_hsa_circ_281818,RMVar_hsa_circ_173873,RMVar_hsa_circ_173874 96842 RMVar_ID_96842 Human_SNP_ID_583225840 m1A Human chr15 + 74620059 74620059 74620059 CCAGAGGAGGTACCGGGAGCGCCGTGACAGCGATACATACCGGTGTGAAGAGCGGAGCCCATCCT CCAGAGGAGGTACCGGGAGCGCCGTGACAGCGTTACATACCGGTGTGAAGAGCGGAGCCCATCCT A T CLK3 Ensembl:ENSG00000179335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74619974..74620174 26863196 MeRIP-seq:(Medium) rs1262350031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885773,Human_RBP_ID_9371138,Human_RBP_ID_17870212,Human_RBP_ID_18982407,Human_RBP_ID_26327720 Human_Splice_Rec_1625752,Human_Splice_Rec_1625776,Human_Splice_Rec_1625798,Human_Splice_Rec_1625802,Human_Splice_Rec_1625826,Human_Splice_Rec_1625848,Human_Splice_Rec_1625860,Human_Splice_Rec_1625870,Human_Splice_Rec_1625880,Human_Splice_Rec_1625886,Human_Splice_Rec_1625896,Human_Splice_Rec_1625908,Human_Splice_Rec_1625910,Human_Splice_Rec_1625914 Human_miRNA_ID_2576612 RMVar_hsa_circ_320709,RMVar_hsa_circ_361241,RMVar_hsa_circ_370113,RMVar_hsa_circ_346961,RMVar_hsa_circ_281818,RMVar_hsa_circ_50702,RMVar_hsa_circ_173873,RMVar_hsa_circ_173874,RMVar_hsa_circ_79814,RMVar_hsa_circ_173875 96843 RMVar_ID_96843 Human_SNP_ID_583226451 m1A Human chr15 + 74622169 74622169 74622169 TAAGCGCAGCAGCCGGAGTGTGGAAGATGACAAGGAGGGTCACCTGGTGTGCCGGATCGGCGATT TAAGCGCAGCAGCCGGAGTGTGGAAGATGACAGGGAGGGTCACCTGGTGTGCCGGATCGGCGATT A G CLK3 Ensembl:ENSG00000179335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74622074..74622200 26863196 MeRIP-seq:(Medium) rs767593875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42817,Human_RBP_ID_232373,Human_RBP_ID_463462,Human_RBP_ID_885111,Human_RBP_ID_3945706,Human_RBP_ID_8804124,Human_RBP_ID_12589356,Human_RBP_ID_17870872,Human_RBP_ID_18189677,Human_RBP_ID_18981648,Human_RBP_ID_23666385,Human_RBP_ID_24544120,Human_RBP_ID_26326927 Human_Splice_Rec_1625754,Human_Splice_Rec_1625755,Human_Splice_Rec_1625804,Human_Splice_Rec_1625805,Human_Splice_Rec_1625827,Human_Splice_Rec_1625862,Human_Splice_Rec_1625863,Human_Splice_Rec_1625888,Human_Splice_Rec_1625898,Human_Splice_Rec_1625899,Human_Splice_Rec_1625916,Human_Splice_Rec_1625917,Human_Splice_Rec_1625939 RMVar_hsa_circ_320709,RMVar_hsa_circ_361241,RMVar_hsa_circ_370113,RMVar_hsa_circ_346961,RMVar_hsa_circ_173873,RMVar_hsa_circ_79814,RMVar_hsa_circ_173875 96844 RMVar_ID_96844 Human_SNP_ID_583230535 m1A Human chr15 - 74638158 74638158 74638158 CGTCGGCATGTAAGGCACAGTTAGAAGGATGAAGAAGAAGGCAGGAGAGGTAAGAAACCAAGAGG CGTCGGCATGTAAGGCACAGTTAGAAGGATGACGAAGAAGGCAGGAGAGGTAAGAAACCAAGAGG T G EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:74637946..74638307;chr15:74637890..74638300;chr15:74637927..74638284 26863196 MeRIP-seq:(Medium) rs1393067532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814927,Human_RBP_ID_6462986,Human_RBP_ID_12589666 RMVar_hsa_circ_11548,RMVar_hsa_circ_52538,RMVar_hsa_circ_305729,RMVar_hsa_circ_23128,RMVar_hsa_circ_173881 96845 RMVar_ID_96845 Human_SNP_ID_583243884 m1A Human chr15 - 74695984 74695984 74695984 GCTTCCGGCAGCGGCGGCGGTGGTGAAGGCCGATGCTGTGGGGGTGGGCGTGGAGAGAATTCTTC GCTTCCGGCAGCGGCGGCGGTGGTGAAGGCCGGTGCTGTGGGGGTGGGCGTGGAGAGAATTCTTC T C EDC3 Ensembl:ENSG00000179151 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74695802..74696025 26863196 MeRIP-seq:(Medium) rs1307332315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760002,Human_RBP_ID_4342815,Human_RBP_ID_6463271,Human_RBP_ID_23666515,Human_RBP_ID_25165346 96846 RMVar_ID_96846 Human_SNP_ID_583261633 m1A Human chr15 + 74760549 74760541 74760550 TGCCCACCTCTCCTCACACCCACACTACAAAGAAAATTATCTTTGCTCTCATCTTTTCCCGTGAC TGCCCACCTCTCCTCACACCCACAC_________AATTATCTTTGCTCTCATCTTTTCCCGTGAC CTACAAAGAA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74760510..74760635 26863196 MeRIP-seq:(Medium) rs1402542000 Functional Loss DEL dbSNP153 26..34 33 - - - 96847 RMVar_ID_96847 Human_SNP_ID_583261641 m1A Human chr15 + 74760549 74760549 74760549 TGCCCACCTCTCCTCACACCCACACTACAAAGAAAATTATCTTTGCTCTCATCTTTTCCCGTGAC TGCCCACCTCTCCTCACACCCACACTACAAAGGAAATTATCTTTGCTCTCATCTTTTCCCGTGAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74760510..74760635 26863196 MeRIP-seq:(Medium) rs1179815002 Functional Loss SNV dbSNP153 33..33 33 - - - 96848 RMVar_ID_96848 Human_SNP_ID_583267134 m1A Human chr15 - 74782176 74782158 74782176 AGGCGCGGGTGGGGCAGGAGCGGGAGGGCGGCAGCGGGCTCGGCGGCGGCGGCGGCCAACCTCGG AGGCGCGGGTGGGGCAGGAGCGGGAGGGCGGC__________________GGCGGCCAACCTCGG CGCCGCCGCCGAGCCCGCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74782129..74782260 26863196 MeRIP-seq:(Medium) rs1266010652 Functional Loss DEL dbSNP153 33..50 33 - - - 96849 RMVar_ID_96849 Human_SNP_ID_583267139 m1A Human chr15 + 74782169 74782169 74782169 GGGCGAGCCGAGGTTGGCCGCCGCCGCCGCCGAGCCCGCTGCCGCCCTCCCGCTCCTGCCCCACC GGGCGAGCCGAGGTTGGCCGCCGCCGCCGCCGGGCCCGCTGCCGCCCTCCCGCTCCTGCCCCACC A G CSK Ensembl:ENSG00000103653 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:74782120..74782451 26863196 MeRIP-seq:(Medium) rs1228701097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342391,Human_RBP_ID_5316297,Human_RBP_ID_18418504 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 96850 RMVar_ID_96850 Human_SNP_ID_583267146 m1A Human chr15 + 74782199 74782199 74782199 CGAGCCCGCTGCCGCCCTCCCGCTCCTGCCCCACCCGCGCCTTGCCCGGGGGCTTCTGCCGGGGT CGAGCCCGCTGCCGCCCTCCCGCTCCTGCCCCCCCCGCGCCTTGCCCGGGGGCTTCTGCCGGGGT A C CSK Ensembl:ENSG00000103653 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:74782148..74782400 26863196 MeRIP-seq:(Medium) rs1040164237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4333360,Human_RBP_ID_5316297,Human_RBP_ID_5439876,Human_RBP_ID_5494724,Human_RBP_ID_18418504 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 96851 RMVar_ID_96851 Human_SNP_ID_583267178 m1A Human chr15 + 74782351 74782351 74782351 CCGCCGGAGCCCGCGGGGCGTGGAGCGCGAGGAGCCCCGCGGCCCCGATCGAGCGTCCGGGGCGG CCGCCGGAGCCCGCGGGGCGTGGAGCGCGAGGTGCCCCGCGGCCCCGATCGAGCGTCCGGGGCGG A T CSK Ensembl:ENSG00000103653 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74782314..74782448 26863196 MeRIP-seq:(Medium) rs1249076621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342393,Human_RBP_ID_5439878,Human_RBP_ID_5523450,Human_RBP_ID_22934785 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 96852 RMVar_ID_96852 Human_SNP_ID_583267196 m1A Human chr15 - 74782406 74782399 74782406 TTCCGAGCGCCGCCACTGAGGTTCGATTTTGGAACGTCGCGCTGGCTGCCGGGGGCCGCCCCGGA TTCCGAGCGCCGCCACTGAGGTTCGATTTTGG_______CGCTGGCTGCCGGGGGCCGCCCCGGA GCGACGTT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:74782076..74782474 26863410 MeRIP-seq:(Medium) rs1365544433 Functional Loss DEL dbSNP153 33..39 33 - - - 96853 RMVar_ID_96853 Human_SNP_ID_583267222 m1A Human chr15 - 74782470 74782467 74782471 AGGGGGCGGGAGGGAGTCGGGGGGAGGAAACAATGTAGCCGGCGCGGCCCCGGCAGAGTTCCGCT AGGGGGCGGGAGGGAGTCGGGGGGAGGAAAC____TAGCCGGCGCGGCCCCGGCAGAGTTCCGCT ACATT A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:74782376..74782641 26863196 MeRIP-seq:(Medium) rs1269423107 Functional Loss DEL dbSNP153 32..35 33 - - - 96854 RMVar_ID_96854 Human_SNP_ID_583267225 m1A Human chr15 - 74782470 74782470 74782470 AGGGGGCGGGAGGGAGTCGGGGGGAGGAAACAATGTAGCCGGCGCGGCCCCGGCAGAGTTCCGCT AGGGGGCGGGAGGGAGTCGGGGGGAGGAAACAGTGTAGCCGGCGCGGCCCCGGCAGAGTTCCGCT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:74782376..74782641 26863196 MeRIP-seq:(Medium) rs1181373415 Functional Loss SNV dbSNP153 33..33 33 - - - 96855 RMVar_ID_96855 Human_SNP_ID_583272610 m1A Human chr15 + 74802535 74802535 74802535 TGCACCTGTGACGGCTGGCCTCCGCCTGGGTCATGGGCCTGTGGGGACTGAACCTGGAAGATCAT TGCACCTGTGACGGCTGGCCTCCGCCTGGGTCTTGGGCCTGTGGGGACTGAACCTGGAAGATCAT A T CSK Ensembl:ENSG00000103653 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs762082239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463533,Human_RBP_ID_4347404,Human_RBP_ID_6463377,Human_RBP_ID_8422641,Human_RBP_ID_8802197,Human_RBP_ID_12590974,Human_RBP_ID_22799285,Human_RBP_ID_26934470,Human_RBP_ID_27234016,Human_RBP_ID_27559642 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891,RMVar_hsa_circ_124453,RMVar_hsa_circ_173893,RMVar_hsa_circ_94074,RMVar_hsa_circ_103756,RMVar_hsa_circ_173895,RMVar_hsa_circ_173897 96856 RMVar_ID_96856 Human_SNP_ID_583272821 m1A Human chr15 - 74803109 74803109 74803109 ATTCCATCTCACAAGGCGGGTGGGCGGGTGGCAGCGGCACACGAAATCCAAGCCCCTGACAGACG ATTCCATCTCACAAGGCGGGTGGGCGGGTGGCCGCGGCACACGAAATCCAAGCCCCTGACAGACG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74803060..74803136 26863196 MeRIP-seq:(Medium) rs1455826771 Functional Loss SNV dbSNP153 33..33 33 - - - 96857 RMVar_ID_96857 Human_SNP_ID_583279338 m1A Human chr15 + 74826853 74826853 74826853 AGCCGGGAGGAGTACGAGGAGTATCAGAAGCAACTCGTGGAAGAGAAGTGAGTGGGATCCCTTCC AGCCGGGAGGAGTACGAGGAGTATCAGAAGCACCTCGTGGAAGAGAAGTGAGTGGGATCCCTTCC A C CPLX3,AC091230.1 Ensembl:ENSG00000213578,Ensembl:ENSG00000261606 Protein coding,lincRNA CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74826803..74826868 26863196 MeRIP-seq:(Medium) rs370055180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5570067 Human_Splice_Rec_1626561,Human_Splice_Rec_1626571,Human_Splice_Rec_1626575 96858 RMVar_ID_96858 Human_SNP_ID_583284559 m1A Human chr15 - 74844515 74844515 74844515 CTCAAGCTCTTCTCTGCCTCATAAACGGATCCAGAGAAGGCTGGTTGCCTTAAGCTCTTCCCTGC CTCAAGCTCTTCTCTGCCTCATAAACGGATCCCGAGAAGGCTGGTTGCCTTAAGCTCTTCCCTGC T G SCAMP2 Ensembl:ENSG00000140497 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:74844379..74844530 32194978 MeRIP-seq:(Medium) rs1232230554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463609,Human_RBP_ID_1002032,Human_RBP_ID_1834113,Human_RBP_ID_12591193,Human_RBP_ID_17251097,Human_RBP_ID_17366303,Human_RBP_ID_18436814,Human_RBP_ID_18668235 Human_miRNA_ID_954854 96859 RMVar_ID_96859 Human_SNP_ID_583284664 m1A Human chr15 + 74844929 74844929 74844929 AGGGGGAAAAAATTCCCTGTCCCTCCCGTTCCAGGGAGAGCTGGTCGCTGAGGGAGGAGGAAGAG AGGGGGAAAAAATTCCCTGTCCCTCCCGTTCCGGGGAGAGCTGGTCGCTGAGGGAGGAGGAAGAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:74844879..74845030 32194978 MeRIP-seq:(Medium) rs959156321 Functional Loss SNV dbSNP153 33..33 33 - - - 96860 RMVar_ID_96860 Human_SNP_ID_583286351 m1A Human chr15 + 74851481 74851481 74851481 ACGAGGGCAGAGGGGGCCAGTTGTTCTGTCTCACTGGGTAGGGCAAAAAGAGTGACGAGGTAAGG ACGAGGGCAGAGGGGGCCAGTTGTTCTGTCTCTCTGGGTAGGGCAAAAAGAGTGACGAGGTAAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr15:74851437..74851526;chr15:74848611..74851923 26863196,32194978 MeRIP-seq:(Medium) rs1191435201 Functional Loss SNV dbSNP153 33..33 33 - - - 96861 RMVar_ID_96861 Human_SNP_ID_583286525 m1A Human chr15 - 74852172 74852172 74852172 CTCCCCTGTTCTCTCCAGGCCGTGGTGTCTGCAGCCCAGGCAGGCCTGCTCCGGCAGCAGGAAGA CTCCCCTGTTCTCTCCAGGCCGTGGTGTCTGCCGCCCAGGCAGGCCTGCTCCGGCAGCAGGAAGA T G SCAMP2 Ensembl:ENSG00000140497 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:74852121..74852222 32194978 MeRIP-seq:(Medium) rs749239838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759037,Human_RBP_ID_887754,Human_RBP_ID_5354576,Human_RBP_ID_22440116,Human_RBP_ID_22650862,Human_RBP_ID_26809599 Human_Splice_Rec_1626996,Human_Splice_Rec_1627010,Human_Splice_Rec_1627054,Human_Splice_Rec_1627076,Human_Splice_Rec_1627086,Human_Splice_Rec_1627100,Human_Splice_Rec_1627110 RMVar_hsa_circ_8392,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_8207,RMVar_hsa_circ_351304,RMVar_hsa_circ_111829,RMVar_hsa_circ_17930,RMVar_hsa_circ_173904,RMVar_hsa_circ_39023 96862 RMVar_ID_96862 Human_SNP_ID_583291947 m1A Human chr15 + 74873306 74873306 74873306 GGCGAACTCCGCGAACGCTGCTGCCTCCGGGCACCCAGACCCAGCGGCGCTTCGTGTAGACCCTC GGCGAACTCCGCGAACGCTGCTGCCTCCGGGCCCCCAGACCCAGCGGCGCTTCGTGTAGACCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74873153..74873312 26863196 MeRIP-seq:(Medium) rs1166585538 Functional Loss SNV dbSNP153 33..33 33 - - - 96863 RMVar_ID_96863 Human_SNP_ID_583296563 m1A Human chr15 - 74890108 74890108 74890108 CCAGGACGCGCTCCACGAACACACTCGCCGACACCCCAGCCAATGGCTCACCTCGCGGAGCGGCC CCAGGACGCGCTCCACGAACACACTCGCCGACCCCCCAGCCAATGGCTCACCTCGCGGAGCGGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74890097..74890219 26863196 MeRIP-seq:(Medium) rs767587896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8422679 96864 RMVar_ID_96864 Human_SNP_ID_583298859 m1A Human chr15 - 74897235 74897235 74897235 GAGATTTTCATGGCACACGAAGGACACCCATCATAGCCCCTCACTCACCTCCGTCTTCATAATGG GAGATTTTCATGGCACACGAAGGACACCCATCGTAGCCCCTCACTCACCTCCGTCTTCATAATGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:74897224..74897325 32194978 MeRIP-seq:(Medium) rs1420219001 Functional Loss SNV dbSNP153 33..33 33 - - - 96865 RMVar_ID_96865 Human_SNP_ID_583298965 m1A Human chr15 - 74897573 74897573 74897573 TGGGTGTGCTGGCTATTACTGTCCCCTGTACCATCAGGAGGATGCTGGCAGAGTCCAGTGCCAAG TGGGTGTGCTGGCTATTACTGTCCCCTGTACCTTCAGGAGGATGCTGGCAGAGTCCAGTGCCAAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:74897524..74897675 32194978 MeRIP-seq:(Medium) rs1398311778 Functional Loss SNV dbSNP153 33..33 33 - - - 96866 RMVar_ID_96866 Human_SNP_ID_583301397 m1A Human chr15 - 74906702 74906702 74906702 GCTCGGGACCGCGCGCCGGGAGCTGCGGGGCCACCCTCCGGGCAGATCGGTAATAGAGCCCTCCG GCTCGGGACCGCGCGCCGGGAGCTGCGGGGCCCCCCTCCGGGCAGATCGGTAATAGAGCCCTCCG T G FAM219B Ensembl:ENSG00000178761 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74906657..74906790 26863196 MeRIP-seq:(Medium) rs145289460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463733,Human_RBP_ID_4342824,Human_RBP_ID_18418395 96867 RMVar_ID_96867 Human_SNP_ID_583305083 m1A Human chr15 - 74920444 74920444 74920444 TTTCCTGGCTAATTCTTTGTGTTTTCTCTTACAGATGGGCTTCCCCAAGGATTTATTGACATTGC TTTCCTGGCTAATTCTTTGTGTTTTCTCTTACGGATGGGCTTCCCCAAGGATTTATTGACATTGC T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74920420..74920491 26863196 MeRIP-seq:(Medium) rs113648863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885124,Human_RBP_ID_4333835,Human_RBP_ID_6463636,Human_RBP_ID_22439879,Human_RBP_ID_22579849,Human_RBP_ID_24368479 RMVar_hsa_circ_96096,RMVar_hsa_circ_112108,RMVar_hsa_circ_173913,RMVar_hsa_circ_173914 96868 RMVar_ID_96868 Human_SNP_ID_583306839 m1A Human chr15 - 74926889 74926889 74926889 GAGGTTGACATGGCCCTTCTTTTTAATTTTGCAGGGATAAACACACTTGTTACCTATGATATGGT GAGGTTGACATGGCCCTTCTTTTTAATTTTGCGGGGATAAACACACTTGTTACCTATGATATGGT T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74926716..74926946 26863196 MeRIP-seq:(Medium) rs1218244748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4347493,Human_RBP_ID_22439880 RMVar_hsa_circ_96096,RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173913,RMVar_hsa_circ_173914,RMVar_hsa_circ_278450,RMVar_hsa_circ_173916,RMVar_hsa_circ_173915,RMVar_hsa_circ_287144,RMVar_hsa_circ_173919,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 96869 RMVar_ID_96869 Human_SNP_ID_583307442 m1A Human chr15 + 74929231 74929231 74929231 GACCCATGGGAATAGCAGCGAACTGACTGGATAGCTATAATGTGAAAGAACCATAACTTCAATGT GACCCATGGGAATAGCAGCGAACTGACTGGATGGCTATAATGTGAAAGAACCATAACTTCAATGT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:74929101..74937738 26863410 MeRIP-seq:(Medium) rs773308546 Functional Loss SNV dbSNP153 33..33 33 - - - 96870 RMVar_ID_96870 Human_SNP_ID_583309827 m1A Human chr15 + 74937904 74937903 74937904 GCAAGGACACGAGGGCGCGGGCAGTGGCAAGCAGGGGCCTTACCCACGGCGGGGCCGGGGGTCCG GCAAGGACACGAGGGCGCGGGCAGTGGCAAGC_GGGGCCTTACCCACGGCGGGGCCGGGGGTCCG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:74937901..74938071 32194978 MeRIP-seq:(Medium) rs930808006 Functional Loss DEL dbSNP153 33..33 33 - - - 96871 RMVar_ID_96871 Human_SNP_ID_583309886 m1A Human chr15 + 74938052 74938052 74938052 CGATGGCGGCGCGCGGGCTGAGGACAGAGAGAAGCCGGTGTAAGCTCGCGGGTTGCTCCGGAGCG CGATGGCGGCGCGCGGGCTGAGGACAGAGAGAGGCCGGTGTAAGCTCGCGGGTTGCTCCGGAGCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:74938001..74938075 26863196 MeRIP-seq:(Medium) rs1196288368 Functional Loss SNV dbSNP153 33..33 33 - - - 96872 RMVar_ID_96872 Human_SNP_ID_583314535 m1A Human chr15 - 74956364 74956362 74956364 GCGCCATCGTCTTCAGCGGCTGCGGCCGGGCCACCACCAAAACCGTCACGTGCGCCGAGATCCTC GCGCCATCGTCTTCAGCGGCTGCGGCCGGGCC__CACCAAAACCGTCACGTGCGCCGAGATCCTC GGT G RPP25 Ensembl:ENSG00000178718 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:74956264..74956753 26863410 MeRIP-seq:(Medium) rs1455448198 Functional Loss DEL dbSNP153,HGVD 33..34 33 - - - 96873 RMVar_ID_96873 Human_SNP_ID_583314586 m1A Human chr15 + 74956471 74956471 74956471 GGTTCCGGATCTTGCTGCCTTCCTTGACCCGCATGTGCACCGCGCCCGGCGCCAGGTCTGCGAAG GGTTCCGGATCTTGCTGCCTTCCTTGACCCGCGTGTGCACCGCGCCCGGCGCCAGGTCTGCGAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74955901..74956800 26863196 MeRIP-seq:(Medium) rs757839023 Functional Loss SNV dbSNP153 33..33 33 - - - 96874 RMVar_ID_96874 Human_SNP_ID_583314989 m1A Human chr15 - 74957338 74957338 74957338 CCGGGAGCCTCGAGCTCCGGGCAGGCGTGGCGAGGCTGAAGTCTGGGTCTTCCGCGCCCCGCGAG CCGGGAGCCTCGAGCTCCGGGCAGGCGTGGCGGGGCTGAAGTCTGGGTCTTCCGCGCCCCGCGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:74957290..74957381 26863196 MeRIP-seq:(Medium) rs1383152606 Functional Loss SNV dbSNP153 33..33 33 - - - 96875 RMVar_ID_96875 Human_SNP_ID_735254841 m1A Human chrX + 150363336 150363336 150363336 GAATGGAGCGAGCAGATTGAGGCCGCCACTGCAGCGCCGCCAGCATGAACTTGGCCGCGAGCTGA GAATGGAGCGAGCAGATTGAGGCCGCCACTGCGGCGCCGCCAGCATGAACTTGGCCGCGAGCTGA A G MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150363285..150363527 26863196 MeRIP-seq:(Medium) rs1367781155 Functional Loss SNV dbSNP153 33..33 33 - - - 96876 RMVar_ID_96876 Human_SNP_ID_735254843 m1A Human chrX - 150363349 150363349 150363349 GCCGCCGGCCGCTTCAGCTCGCGGCCAAGTTCATGCTGGCGGCGCTGCAGTGGCGGCCTCAATCT GCCGCCGGCCGCTTCAGCTCGCGGCCAAGTTCTTGCTGGCGGCGCTGCAGTGGCGGCCTCAATCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:150363299..150363458 26863196 MeRIP-seq:(Medium) rs899286879 Functional Loss SNV dbSNP153 33..33 33 - - - 96877 RMVar_ID_96877 Human_SNP_ID_735254844 m1A Human chrX - 150363349 150363349 150363349 GCCGCCGGCCGCTTCAGCTCGCGGCCAAGTTCATGCTGGCGGCGCTGCAGTGGCGGCCTCAATCT GCCGCCGGCCGCTTCAGCTCGCGGCCAAGTTCCTGCTGGCGGCGCTGCAGTGGCGGCCTCAATCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:150363299..150363458 26863196 MeRIP-seq:(Medium) rs899286879 Functional Loss SNV dbSNP153 33..33 33 - - - 96878 RMVar_ID_96878 Human_SNP_ID_735261691 m1A Human chrX + 150398379 150398355 150398379 GAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAAGAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA GAGGAAGAG________________________GAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA GGAAGAGGAAGAGGAAGAGGAAGAA G MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150398368..150398433 26863196 MeRIP-seq:(Medium) rs1569564638 Functional Loss DEL dbSNP153 10..33 33 - - - 96879 RMVar_ID_96879 Human_SNP_ID_735261696 m1A Human chrX + 150398379 150398361 150398379 GAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAAGAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA GAGGAAGAGGAAGAG__________________GAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA GGAAGAGGAAGAGGAAGAA G MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150398368..150398433 26863196 MeRIP-seq:(Medium) rs1569564641 Functional Loss DEL dbSNP153 16..33 33 - - - 96880 RMVar_ID_96880 Human_SNP_ID_735261711 m1A Human chrX + 150398379 150398379 150398379 GAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAAGAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA GAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAGGAAGAAGAAGAAGAAGAAGACAGGGA A G MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150398368..150398433 26863196 MeRIP-seq:(Medium) rs868919377 Functional Loss SNV dbSNP153 33..33 33 - - - 96881 RMVar_ID_96881 Human_SNP_ID_735262840 m1A Human chrX + 150403903 150403897 150403904 AAAGAAAGGAAAGAAAGAAGAAAGAAAAAGAAAGAAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAAGAAAGGAAAGAAAGAAGAAAGAAA_______AAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAAGAAAG A MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:150403786..150404119 26863196 MeRIP-seq:(Medium) rs1490748248 Functional Loss DEL dbSNP153 28..34 33 - - - 96882 RMVar_ID_96882 Human_SNP_ID_735262842 m1A Human chrX + 150403903 150403901 150403904 AAAGAAAGGAAAGAAAGAAGAAAGAAAAAGAAAGAAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAAGAAAGGAAAGAAAGAAGAAAGAAAAAGA___AAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAAG A MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:150403786..150404119 26863196 MeRIP-seq:(Medium) rs1352064684 Functional Loss DEL dbSNP153 32..34 33 - - - 96883 RMVar_ID_96883 Human_SNP_ID_735262844 m1A Human chrX + 150403903 150403902 150403904 AAAGAAAGGAAAGAAAGAAGAAAGAAAAAGAAAGAAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAAGAAAGGAAAGAAAGAAGAAAGAAAAAGAA__AAGAAAGAAAAAGAAAGAAAGACAGAGAAAG AAG A MAMLD1 Ensembl:ENSG00000013619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:150403786..150404119 26863196 MeRIP-seq:(Medium) rs1263088302 Functional Loss DEL dbSNP153 33..34 33 - - - 96884 RMVar_ID_96884 Human_SNP_ID_735274390 m1A Human chrX - 150470875 150470875 150470875 GACATCAGGTGTCCTTGAGGGGTTTTGATGGTAGAGGACATGAGGTTGGCAAGAATGGAGCTCTG GACATCAGGTGTCCTTGAGGGGTTTTGATGGTTGAGGACATGAGGTTGGCAAGAATGGAGCTCTG T A HSALNG0140639 RNACentral:URS0000EC090F lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:150470829..150471015 26863196 MeRIP-seq:(Medium) rs370799290 Functional Loss SNV dbSNP153 33..33 33 - - - 96885 RMVar_ID_96885 Human_SNP_ID_735318552 m1A Human chrX + 150736208 150736208 150736208 GACTGTGTCCTTAGAAGAAGAGGAGAAGAGACAGACACAGACAAAGGAAAGAAGGTCAGGTGGAA GACTGTGTCCTTAGAAGAAGAGGAGAAGAGACGGACACAGACAAAGGAAAGAAGGTCAGGTGGAA A G MTMR1 Ensembl:ENSG00000063601 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150736173..150736278 26863196 MeRIP-seq:(Medium) rs1284814323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297901,RMVar_hsa_circ_349524,RMVar_hsa_circ_335151,RMVar_hsa_circ_313679,RMVar_hsa_circ_299547,RMVar_hsa_circ_66747,RMVar_hsa_circ_294951,RMVar_hsa_circ_319871,RMVar_hsa_circ_306427,RMVar_hsa_circ_355686,RMVar_hsa_circ_264121,RMVar_hsa_circ_264122,RMVar_hsa_circ_69635 96886 RMVar_ID_96886 Human_SNP_ID_735324130 m1A Human chrX - 150766499 150766499 150766499 GTGCGTGGCTTCTGGGGTGGGACCCAGAGGGGAGGCTCTGGGACAGGGGCTGGGGTTCAGTGCCA GTGCGTGGCTTCTGGGGTGGGACCCAGAGGGGGGGCTCTGGGACAGGGGCTGGGGTTCAGTGCCA T C CD99L2 Ensembl:ENSG00000102181 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:150766465..150766589 26863196 MeRIP-seq:(Medium) rs1192093746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257243,Human_RBP_ID_5155521,Human_RBP_ID_18147299,Human_RBP_ID_24333766,Human_RBP_ID_26573981 RMVar_hsa_circ_75688,RMVar_hsa_circ_264127 96887 RMVar_ID_96887 Human_SNP_ID_735324727 m1A Human chrX - 150769006 150769006 150769006 TCTGAGGGCCCTGTCCAGCTGCAGGCATGCACAATGGTGCCACCGCTTGTCACCCGGCTCCCCCC TCTGAGGGCCCTGTCCAGCTGCAGGCATGCACGATGGTGCCACCGCTTGTCACCCGGCTCCCCCC T C CD99L2 Ensembl:ENSG00000102181 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:150768957..150769053 26863196 MeRIP-seq:(Medium) rs200033765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186459,Human_RBP_ID_730584,Human_RBP_ID_5055379 Human_Splice_Rec_2242441,Human_Splice_Rec_2242461,Human_Splice_Rec_2242482,Human_Splice_Rec_2242496,Human_Splice_Rec_2242510,Human_Splice_Rec_2242526,Human_Splice_Rec_2242542 RMVar_hsa_circ_75688,RMVar_hsa_circ_264127 96888 RMVar_ID_96888 Human_SNP_ID_735348029 m1A Human chrX + 150898271 150898271 150898271 TACACCTGCTCGTTCAGGATTTTAGGGGGCCCATCCCGCTGTTTCCAGCCCAGCGTCAGGAGGGG TACACCTGCTCGTTCAGGATTTTAGGGGGCCCGTCCCGCTGTTTCCAGCCCAGCGTCAGGAGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:150898269..150898363;chrX:150898265..150898391 26863196 MeRIP-seq:(Medium) rs1233485695 Functional Loss SNV dbSNP153 33..33 33 - - - 96889 RMVar_ID_96889 Human_SNP_ID_735364247 m1A Human chrX - 150983348 150983348 150983348 GTACCTGTATTGTTCGCTAGTCTGGGCAGCGCAGGGCACGACGCGCGGCTCAGCGCTCCCCAGCC GTACCTGTATTGTTCGCTAGTCTGGGCAGCGCGGGGCACGACGCGCGGCTCAGCGCTCCCCAGCC T C RF00017-4497,RF00017-071,RF00017-1190 RNACentral:URS0000961FEC,RNACentral:URS00009310A4,RNACentral:URS000092EF5C SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:150983301..150983899 26863196 MeRIP-seq:(Medium) rs1399003680 Functional Loss SNV dbSNP153 33..33 33 - - - 96890 RMVar_ID_96890 Human_SNP_ID_735364268 m1A Human chrX - 150983397 150983395 150983398 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGCGGGCGGTGCGAGACGTACCTGTATTGTTCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG___CGGGCGGTGCGAGACGTACCTGTATTGTTCG GCTC G RF00017-4497,RF00017-071,RF00017-1190 RNACentral:URS0000961FEC,RNACentral:URS00009310A4,RNACentral:URS000092EF5C SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chrX:150983315..150985543;chrX:150983313..150983604;chrX:150983324..150983524 26863196 MeRIP-seq:(Medium) rs1414279750 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_7985698,Human_RBP_ID_26742905 96891 RMVar_ID_96891 Human_SNP_ID_735365361 m1A Human chrX + 150987831 150987831 150987831 AAGGAAAGTTTGATGGTGCAAAGGGTCCTGCTAAAGTTGCCCGGAAAAAGGTGGAAGAGGAAGAT AAGGAAAGTTTGATGGTGCAAAGGGTCCTGCTCAAGTTGCCCGGAAAAAGGTGGAAGAGGAAGAT A C HMGB3 Ensembl:ENSG00000029993 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:150987778..150987950 26863196 MeRIP-seq:(Medium) rs1557425289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_730600,Human_RBP_ID_5055442,Human_RBP_ID_7985702,Human_RBP_ID_9244718,Human_RBP_ID_24333919,Human_RBP_ID_26363432,Human_RBP_ID_27834221 Human_Splice_Rec_2242579,Human_Splice_Rec_2242587,Human_Splice_Rec_2242595,Human_Splice_Rec_2242603 Human_miRNA_ID_2529023 RMVar_hsa_circ_103141,RMVar_hsa_circ_86790,RMVar_hsa_circ_264140,RMVar_hsa_circ_264141,RMVar_hsa_circ_80193,RMVar_hsa_circ_264142 96892 RMVar_ID_96892 Human_SNP_ID_735466668 m1A Human chrX - 151562856 151562855 151562857 CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCCGACCCCCGACCCCCCGCCCCCCGCCCCCCCACCC CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCC__CCCCCGACCCCCCGCCCCCCGCCCCCCCACCC GTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chrX:151562790..151562864;chrX:151562734..151562868;chrX:151562791..151562860 26863196 MeRIP-seq:(Medium) rs200658814 Functional Loss DEL dbSNP153 32..33 33 - - - 96893 RMVar_ID_96893 Human_SNP_ID_735466670 m1A Human chrX - 151562856 151562856 151562856 CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCCGACCCCCGACCCCCCGCCCCCCGCCCCCCCACCC CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCCGGCCCCCGACCCCCCGCCCCCCGCCCCCCCACCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chrX:151562790..151562864;chrX:151562734..151562868;chrX:151562791..151562860 26863196 MeRIP-seq:(Medium) rs1453366304 Functional Loss SNV dbSNP153 33..33 33 - - - 96894 RMVar_ID_96894 Human_SNP_ID_735466671 m1A Human chrX - 151562856 151562856 151562856 CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCCGACCCCCGACCCCCCGCCCCCCGCCCCCCCACCC CCCCCCCGCCCCCCCCGCCCCCCGCCCCCCCGCCCCCCGACCCCCCGCCCCCCGCCCCCCCACCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chrX:151562790..151562864;chrX:151562734..151562868;chrX:151562791..151562860 26863196 MeRIP-seq:(Medium) rs1453366304 Functional Loss SNV dbSNP153 33..33 33 - - - 96895 RMVar_ID_96895 Human_SNP_ID_735486981 m1A Human chrX - 151672271 151672271 151672271 TCTTCTTCTCCTGCATCTTCTTCTGCTTCTGCACCTTCCTTTGCTCTCTCAGCTGTTGCAGCTGC TCTTCTTCTCCTGCATCTTCTTCTGCTTCTGCGCCTTCCTTTGCTCTCTCAGCTGTTGCAGCTGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:151672268..151672492 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96896 RMVar_ID_96896 Human_SNP_ID_735486982 m1A Human chrX - 151672271 151672271 151672271 TCTTCTTCTCCTGCATCTTCTTCTGCTTCTGCACCTTCCTTTGCTCTCTCAGCTGTTGCAGCTGC TCTTCTTCTCCTGCATCTTCTTCTGCTTCTGCCCCTTCCTTTGCTCTCTCAGCTGTTGCAGCTGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:151672268..151672492 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96897 RMVar_ID_96897 Human_SNP_ID_735487342 m1A Human chrX + 151673966 151673966 151673966 TCCTGAGGCGTATCAAGGGCCCCCCGTGAACCAGCTGCCATTGATAGATACCTCAAACTCTGAGG TCCTGAGGCGTATCAAGGGCCCCCCGTGAACCGGCTGCCATTGATAGATACCTCAAACTCTGAGG A G PASD1 Ensembl:ENSG00000166049 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:151673955..151674108 26863196 MeRIP-seq:(Medium) rs1352286667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2242669 RMVar_hsa_circ_93154,RMVar_hsa_circ_264146 96898 RMVar_ID_96898 Human_SNP_ID_735487789 m1A Human chrX - 151676147 151676142 151676147 CCCCATTTCCCCTCATCACTGGTCATGAAAGTACTGTTAGCACGGCTTATTTGAGTCACGTTGCT CCCCATTTCCCCTCATCACTGGTCATGAAAGT_____TAGCACGGCTTATTTGAGTCACGTTGCT AACAGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:151676096..151676172 26863196 MeRIP-seq:(Medium) rs1178600609 Functional Loss DEL dbSNP153 33..37 33 - - - 96899 RMVar_ID_96899 Human_SNP_ID_735545447 m1A Human chrX - 151974530 151974530 151974530 TCCATCCCGGGACCCGGGAGCCCTTCGCGCCCAGCTCCCTCTCCCCGGGAGCCGGGACGGCTCCC TCCATCCCGGGACCCGGGAGCCCTTCGCGCCCGGCTCCCTCTCCCCGGGAGCCGGGACGGCTCCC T C GABRE Ensembl:ENSG00000102287 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:151974479..151974630 26863196 MeRIP-seq:(Medium) rs746953151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_968829,Human_RBP_ID_9340312,Human_RBP_ID_17096305,Human_RBP_ID_19027696,Human_RBP_ID_19149688 RMVar_hsa_circ_126608,RMVar_hsa_circ_264151,RMVar_hsa_circ_125971,RMVar_hsa_circ_264157 96900 RMVar_ID_96900 Human_SNP_ID_735545484 m1A Human chrX + 151974619 151974619 151974619 TAAGATGCCTAGGAGGACTGGAAGAACTTTGGACAACATTTCCGCGGAGACCGGCGCGACCACCT TAAGATGCCTAGGAGGACTGGAAGAACTTTGGGCAACATTTCCGCGGAGACCGGCGCGACCACCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:151974538..151974630 26863196 MeRIP-seq:(Medium) rs766932351 Functional Loss SNV dbSNP153 33..33 33 - - - 96901 RMVar_ID_96901 Human_SNP_ID_735669379 m1A Human chrX - 152639780 152639780 152639780 CACAACTCTGTTTTCCAGACTTGGCATATGGCATAAGACACACAGAGAGAGCCTTGCTGGTGTAG CACAACTCTGTTTTCCAGACTTGGCATATGGCGTAAGACACACAGAGAGAGCCTTGCTGGTGTAG T C AC244102.4 Ensembl:ENSG00000287394 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:152639765..152639838 26863196 MeRIP-seq:(Medium) rs1031951134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2243013 96902 RMVar_ID_96902 Human_SNP_ID_735708745 m1A Human chrX - 152898105 152898105 152898105 GGGAGGCAGGCGCGGGGCGCGGGGCGCGGTGCACAGCGGGGAGCGCGCAGGGAGGCGAGGAGGCG GGGAGGCAGGCGCGGGGCGCGGGGCGCGGTGCCCAGCGGGGAGCGCGCAGGGAGGCGAGGAGGCG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:152898068..152898207 26863196 MeRIP-seq:(Medium) rs1290290401 Functional Loss SNV dbSNP153 33..33 33 - - - 96903 RMVar_ID_96903 Human_SNP_ID_735716411 m1A Human chrX - 152938165 152938165 152938165 CCCAGAAGTTCAGCACTGTCTGCTCATGCCTTACCCCTTTGGGTCTGCCTTTGCATCCTCCTGGG CCCAGAAGTTCAGCACTGTCTGCTCATGCCTTTCCCCTTTGGGTCTGCCTTTGCATCCTCCTGGG T A lnc-PNMA5-4 RNACentral:URS0000D5AD80 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:152938126..152938175 32194978 MeRIP-seq:(Medium) rs1271114754 Functional Loss SNV dbSNP153 33..33 33 - - - 96904 RMVar_ID_96904 Human_SNP_ID_735777431 m1A Human chrX - 153334312 153334312 153334312 CTCCGCCCTGCGGCCCCTCCAGCGCCCCCCGCACATCCTCCCGCGGCCCGCACACTCACCCAGGC CTCCGCCCTGCGGCCCCTCCAGCGCCCCCCGCGCATCCTCCCGCGGCCCGCACACTCACCCAGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153334283..153334451 26863196 MeRIP-seq:(Medium) rs1460421463 Functional Loss SNV dbSNP153 33..33 33 - - - 96905 RMVar_ID_96905 Human_SNP_ID_735801953 m1A Human chrX - 153447782 153447782 153447782 GATCGAGTTGGCCGAGGATGGATGATTGTGGCAGCAGAAGCCGTTGCAGCCCCACGTTGTGCTCT GATCGAGTTGGCCGAGGATGGATGATTGTGGCCGCAGAAGCCGTTGCAGCCCCACGTTGTGCTCT T G HAUS7,TREX2 Ensembl:ENSG00000213397,Ensembl:ENSG00000183479 Protein coding,Protein coding 3'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153447732..153454878 26863196 MeRIP-seq:(Medium) rs782488488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731006,Human_RBP_ID_9409560,Human_RBP_ID_24334381 RMVar_hsa_circ_77697,RMVar_hsa_circ_264187 96906 RMVar_ID_96906 Human_SNP_ID_735805908 m1A Human chrX + 153467532 153467532 153467532 CTCTCCCACACCTCAACTCCCTGCTCCTGTCCAAACGAGCACCCCGCTGTTACCGTCCCCATCCC CTCTCCCACACCTCAACTCCCTGCTCCTGTCCGAACGAGCACCCCGCTGTTACCGTCCCCATCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153467529..153467634 26863196 MeRIP-seq:(Medium) rs1322472211 Functional Loss SNV dbSNP153 33..33 33 - - - 96907 RMVar_ID_96907 Human_SNP_ID_735806752 m1A Human chrX - 153471124 153471124 153471124 TCTAACTACAGCGTGAGCATGGTGAAGAGAAGACGGAGCCCCGCGCTGGGAGAGGAACGCTTCAG TCTAACTACAGCGTGAGCATGGTGAAGAGAAGCCGGAGCCCCGCGCTGGGAGAGGAACGCTTCAG T G HAUS7 Ensembl:ENSG00000213397 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153471073..153471177 26863196 MeRIP-seq:(Medium) rs1556985285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2243986 96908 RMVar_ID_96908 Human_SNP_ID_735814688 m1A Human chrX + 153508840 153508840 153508840 GGTCCATAAGAATGGGGACAGTGGGCTCTGCCAGGGCTGCCGCACCTGTCCAGACACACATGTTC GGTCCATAAGAATGGGGACAGTGGGCTCTGCCGGGGCTGCCGCACCTGTCCAGACACACATGTTC A G BGN Ensembl:ENSG00000182492 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153508792..153509019 26863196 MeRIP-seq:(Medium) rs1348000371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5232436 Human_miRNA_ID_179396,Human_miRNA_ID_2891484 RMVar_hsa_circ_120269,RMVar_hsa_circ_126439,RMVar_hsa_circ_264188,RMVar_hsa_circ_113944,RMVar_hsa_circ_264189,RMVar_hsa_circ_97169,RMVar_hsa_circ_264190,RMVar_hsa_circ_264191,RMVar_hsa_circ_76729,RMVar_hsa_circ_104632,RMVar_hsa_circ_95155,RMVar_hsa_circ_264192,RMVar_hsa_circ_264193,RMVar_hsa_circ_264194 96909 RMVar_ID_96909 Human_SNP_ID_735834673 m1A Human chrX + 153605495 153605471 153605496 GCTTAAATTAAGAAAGAAAGAAAGAAAAATAAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG GCTTAAATT_________________________AAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG TAAGAAAGAAAGAAAGAAAAATAAAG T AF274858.1 Ensembl:ENSG00000260081 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153605487..153605574 26863196 MeRIP-seq:(Medium) rs1222614421 Functional Loss DEL dbSNP153 10..34 33 - - - 96910 RMVar_ID_96910 Human_SNP_ID_735834681 m1A Human chrX + 153605495 153605492 153605496 GCTTAAATTAAGAAAGAAAGAAAGAAAAATAAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG GCTTAAATTAAGAAAGAAAGAAAGAAAAAT____AAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG TAAAG T AF274858.1 Ensembl:ENSG00000260081 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153605487..153605574 26863196 MeRIP-seq:(Medium) rs1293715881 Functional Loss DEL dbSNP153 31..34 33 - - - 96911 RMVar_ID_96911 Human_SNP_ID_735834682 m1A Human chrX + 153605495 153605492 153605495 GCTTAAATTAAGAAAGAAAGAAAGAAAAATAAAGAAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG GCTTAAATTAAGAAAGAAAGAAAGAAAAAT___GAAGAAAGAAAGAAAGAGAGAGAGAGAGAAAG TAAA T AF274858.1 Ensembl:ENSG00000260081 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153605487..153605574 26863196 MeRIP-seq:(Medium) rs1369137540 Functional Loss DEL dbSNP153 31..33 33 - - - 96912 RMVar_ID_96912 Human_SNP_ID_735843012 m1A Human chrX + 153647228 153647228 153647228 AGTTTCCAAGGTGGAAGCTGGGTCCGGCTGCCAGGAAGCGGCCGGTGCGCGGGCTGCGCGGGCTG AGTTTCCAAGGTGGAAGCTGGGTCCGGCTGCCGGGAAGCGGCCGGTGCGCGGGCTGCGCGGGCTG A G DUSP9 Ensembl:ENSG00000130829 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153647226..153647387 26863196 MeRIP-seq:(Medium) rs1367869186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5075924 96913 RMVar_ID_96913 Human_SNP_ID_735843219 m1A Human chrX + 153648275 153648275 153648275 CCGAGGAGTGGGAGGCCGAGTCGGTGCTGGGCACCCTGCTGCAGAAGCTGCGAGAGGAAGGCTAC CCGAGGAGTGGGAGGCCGAGTCGGTGCTGGGCGCCCTGCTGCAGAAGCTGCGAGAGGAAGGCTAC A G DUSP9 Ensembl:ENSG00000130829 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153648195..153648296 32194978 MeRIP-seq:(Medium) rs895300715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5075934,Human_RBP_ID_22468123 Human_Splice_Rec_2244344,Human_Splice_Rec_2244350 96914 RMVar_ID_96914 Human_SNP_ID_735846054 m1A Human chrX + 153662190 153662190 153662190 CGCCATGAAGGCCCCGGGCACACGACTAGAGTACCAGGTGGTGGGTCGCTGCCTGCCCGCCCCCA CGCCATGAAGGCCCCGGGCACACGACTAGAGTTCCAGGTGGTGGGTCGCTGCCTGCCCGCCCCCA A T RPL18AP16 Ensembl:ENSG00000237793 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153662179..153662353 26863196 MeRIP-seq:(Medium) rs1557037820 Functional Loss SNV dbSNP153 33..33 33 - - - 96915 RMVar_ID_96915 Human_SNP_ID_735851742 m1A Human chrX + 153688031 153688031 153688031 GCCGCCGGGAAGGAGAGGGCGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGC GCCGCCGGGAAGGAGAGGGCGAGGCGCGCCCGCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGC A C SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrX:153687944..153688193 26863410 MeRIP-seq:(Medium) rs1326509179 Functional Loss SNV dbSNP153 33..33 33 - - - 96916 RMVar_ID_96916 Human_SNP_ID_735851752 m1A Human chrX + 153688050 153688032 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAG__________________CCGCCGCCGCCGCCACCACCGCCACCGGAGTC GCCGCCGCCGCCGCCGCCA G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1172726908 Functional Loss DEL dbSNP153 16..33 33 - - - 96917 RMVar_ID_96917 Human_SNP_ID_735851753 m1A Human chrX + 153688050 153688035 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAGCCG_______________CCGCCGCCGCCGCCACCACCGCCACCGGAGTC GCCGCCGCCGCCGCCA G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1475663560 Functional Loss DEL dbSNP153 19..33 33 - - - 96918 RMVar_ID_96918 Human_SNP_ID_735851754 m1A Human chrX + 153688050 153688038 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAGCCGCCG____________CCGCCGCCGCCGCCACCACCGCCACCGGAGTC GCCGCCGCCGCCA G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1373732989 Functional Loss DEL dbSNP153 22..33 33 - - - 96919 RMVar_ID_96919 Human_SNP_ID_735851759 m1A Human chrX + 153688050 153688044 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAGCCGCCGCCGCCG______CCGCCGCCGCCGCCACCACCGCCACCGGAGTC GCCGCCA G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1214765657 Functional Loss DEL dbSNP153 28..33 33 - - - 96920 RMVar_ID_96920 Human_SNP_ID_735851762 m1A Human chrX + 153688050 153688047 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAGCCGCCGCCGCCGCCG___CCGCCGCCGCCGCCACCACCGCCACCGGAGTC GCCA G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1269110152 Functional Loss DEL dbSNP153 31..33 33 - - - 96921 RMVar_ID_96921 Human_SNP_ID_735851766 m1A Human chrX + 153688050 153688050 153688050 CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAGTC CGAGGCGCGCCCGAGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCACCGCCACCGGAGTC A G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chrX:153687974..153688750;chrX:153687959..153688175 26863196,26863410 MeRIP-seq:(Medium) rs1439983213 Functional Loss SNV dbSNP153 33..33 33 - - - 96922 RMVar_ID_96922 Human_SNP_ID_735851866 m1A Human chrX + 153688336 153688335 153688337 CCCGCCGCCGCCCGCGCGCCCCCGGGCCCCCGACACACATGAGATTCTTCAGGCTCACTTTCAAG CCCGCCGCCGCCCGCGCGCCCCCGGGCCCCCG__ACACATGAGATTCTTCAGGCTCACTTTCAAG GAC G SLC6A8 Ensembl:ENSG00000130821 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:153687926..153688550 26863196 MeRIP-seq:(Medium) rs1170591625 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5076821,Human_RBP_ID_5330856,Human_RBP_ID_9340052 96923 RMVar_ID_96923 Human_SNP_ID_735851882 m1A Human chrX - 153688435 153688435 153688435 GGCCGGGGGCCGGGGGGCGGCCGGGCCGGGGGACGGGGCGGCGGGCGGGCGGCGGGGTGCGGGGC GGCCGGGGGCCGGGGGGCGGCCGGGCCGGGGGGCGGGGCGGCGGGCGGGCGGCGGGGTGCGGGGC T C PNCK Ensembl:ENSG00000130822 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chrX:153688376..153688525 26863410 MeRIP-seq:(Medium) rs1303267158 Functional Loss SNV dbSNP153 33..33 33 - - - 96924 RMVar_ID_96924 Human_SNP_ID_735851883 m1A Human chrX - 153688435 153688435 153688435 GGCCGGGGGCCGGGGGGCGGCCGGGCCGGGGGACGGGGCGGCGGGCGGGCGGCGGGGTGCGGGGC GGCCGGGGGCCGGGGGGCGGCCGGGCCGGGGGCCGGGGCGGCGGGCGGGCGGCGGGGTGCGGGGC T G PNCK Ensembl:ENSG00000130822 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chrX:153688376..153688525 26863410 MeRIP-seq:(Medium) rs1303267158 Functional Loss SNV dbSNP153 33..33 33 - - - 96925 RMVar_ID_96925 Human_SNP_ID_735852006 m1A Human chrX - 153688720 153688720 153688720 CCATCTGGCGCGTCCAGGTCTCGCGCGGCGGCACGGCCAGGCGGCCGCCGGGTGTCCCCAGGCCC CCATCTGGCGCGTCCAGGTCTCGCGCGGCGGCGCGGCCAGGCGGCCGCCGGGTGTCCCCAGGCCC T C PNCK Ensembl:ENSG00000130822 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153688675..153688856 26863196 MeRIP-seq:(Medium) rs1557043838 Functional Loss SNV dbSNP153 33..33 33 - - - 96926 RMVar_ID_96926 Human_SNP_ID_735853207 m1A Human chrX + 153693100 153693100 153693100 TACGTGGTCCTGGTCGTGCTGCTGGTGCGTGGAGTGCTGCTGCCTGGCGCCCTGGATGGCATCAT TACGTGGTCCTGGTCGTGCTGCTGGTGCGTGGCGTGCTGCTGCCTGGCGCCCTGGATGGCATCAT A C SLC6A8 Ensembl:ENSG00000130821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153692925..153694025 32194978 MeRIP-seq:(Medium) rs1569539345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257389,Human_RBP_ID_731083,Human_RBP_ID_848441,Human_RBP_ID_968902,Human_RBP_ID_3976859,Human_RBP_ID_7986599,Human_RBP_ID_8715105,Human_RBP_ID_9340071,Human_RBP_ID_17440710,Human_RBP_ID_17553476,Human_RBP_ID_18197381,Human_RBP_ID_18472962,Human_RBP_ID_19027728,Human_RBP_ID_22534593,Human_RBP_ID_23099525 Human_Splice_Rec_2244676,Human_Splice_Rec_2244677,Human_Splice_Rec_2244702,Human_Splice_Rec_2244703,Human_Splice_Rec_2244727,Human_Splice_Rec_2244737 Human_miRNA_ID_2103069,Human_miRNA_ID_2109031,Human_miRNA_ID_2114960,Human_miRNA_ID_2167508,Human_miRNA_ID_2598776,Human_miRNA_ID_2741670,Human_miRNA_ID_3042261 RMVar_hsa_circ_122986,RMVar_hsa_circ_79491,RMVar_hsa_circ_264203,RMVar_hsa_circ_264204 96927 RMVar_ID_96927 Human_SNP_ID_735854044 m1A Human chrX + 153695252 153695252 153695252 CAGCTCACATCACCAGCTCACCTCTGGTAGCCATAGCAGCCCCTGCTTCAGCCCCACCGCACCCC CAGCTCACATCACCAGCTCACCTCTGGTAGCCGTAGCAGCCCCTGCTTCAGCCCCACCGCACCCC A G SLC6A8 Ensembl:ENSG00000130821 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153695201..153695315 26863196 MeRIP-seq:(Medium) rs1158205727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5056053 Human_miRNA_ID_259929,Human_miRNA_ID_263720 RMVar_hsa_circ_87193,RMVar_hsa_circ_264206 96928 RMVar_ID_96928 Human_SNP_ID_735854364 m1A Human chrX + 153696330 153696330 153696330 CCACCCTGTGCGGGGCACACCCCCAGGAAGGGACCCTGGACACGGCTCCCACGTCCAGGCTTAAG CCACCCTGTGCGGGGCACACCCCCAGGAAGGGGCCCTGGACACGGCTCCCACGTCCAGGCTTAAG A G SLC6A8 Ensembl:ENSG00000130821 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153696142..153696443 32194978 MeRIP-seq:(Medium) rs1569539634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731103,Human_RBP_ID_18156013 Human_miRNA_ID_546270,Human_miRNA_ID_581504 RMVar_hsa_circ_87193,RMVar_hsa_circ_264206 96929 RMVar_ID_96929 Human_SNP_ID_735855391 m1A Human chrX + 153700625 153700625 153700625 AAACAAAAAGGGGCTCAAACCAACAGGAAGTCAGCCCCACCGCAAGCCGGACTACAACTAACTCG AAACAAAAAGGGGCTCAAACCAACAGGAAGTCTGCCCCACCGCAAGCCGGACTACAACTAACTCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153700601..153700625 26863196 MeRIP-seq:(Medium) rs1417292662 Functional Loss SNV dbSNP153 33..33 33 - - - 96930 RMVar_ID_96930 Human_SNP_ID_735855672 m1A Human chrX - 153702106 153702106 153702106 CTGTTTTCTTGGTCATTTACATCATTTCAAGAACTAGAGAAAGCTGAAAACCAGGTTCTGGCCAT CTGTTTTCTTGGTCATTTACATCATTTCAAGAGCTAGAGAAAGCTGAAAACCAGGTTCTGGCCAT T C BCAP31 Ensembl:ENSG00000185825 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153702076..153702125 26863196 MeRIP-seq:(Medium) rs1557047470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2244770,Human_Splice_Rec_2244771,Human_Splice_Rec_2244783,Human_Splice_Rec_2244798,Human_Splice_Rec_2244810,Human_Splice_Rec_2244811,Human_Splice_Rec_2244822,Human_Splice_Rec_2244823,Human_Splice_Rec_2244832,Human_Splice_Rec_2244833,Human_Splice_Rec_2244835 RMVar_hsa_circ_100880,RMVar_hsa_circ_108379,RMVar_hsa_circ_119934,RMVar_hsa_circ_110342,RMVar_hsa_circ_103298,RMVar_hsa_circ_91406,RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264211,RMVar_hsa_circ_264213,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215,RMVar_hsa_circ_264212,RMVar_hsa_circ_264209,RMVar_hsa_circ_264210,RMVar_hsa_circ_264208,RMVar_hsa_circ_264216,RMVar_hsa_circ_311555 96931 RMVar_ID_96931 Human_SNP_ID_735856063 m1A Human chrX - 153703960 153703958 153703961 GAAGTACATGGAGGAGAATGACCAGCTCAAGAAGGTGAGCCCAGCTTCCCGACCCACCATGGGGC GAAGTACATGGAGGAGAATGACCAGCTCAAG___GTGAGCCCAGCTTCCCGACCCACCATGGGGC CCTT C BCAP31 Ensembl:ENSG00000185825 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:153703951..153704025;chrX:153703951..153704050 26863196 MeRIP-seq:(Medium) rs782153314 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22777796 Human_Splice_Rec_2244767,Human_Splice_Rec_2244780,Human_Splice_Rec_2244795,Human_Splice_Rec_2244808,Human_Splice_Rec_2244819,Human_Splice_Rec_2244829,Human_Splice_Rec_2244845,Human_Splice_Rec_2244855,Human_Splice_Rec_2244865,Human_Splice_Rec_2244875 Human_miRNA_ID_2866807,Human_miRNA_ID_2866808,Human_miRNA_ID_2866809 RMVar_hsa_circ_100880,RMVar_hsa_circ_108379,RMVar_hsa_circ_110342,RMVar_hsa_circ_91406,RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264211,RMVar_hsa_circ_264213,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215,RMVar_hsa_circ_264212,RMVar_hsa_circ_264210,RMVar_hsa_circ_264216,RMVar_hsa_circ_311555 96932 RMVar_ID_96932 Human_SNP_ID_735856472 m1A Human chrX - 153706126 153706126 153706126 GGGAACCGGGGCCTGGCAGAGGGGAGCCCCAGACTGTCTCAAGGCTGGGAACTGAAGGCCTGGGC GGGAACCGGGGCCTGGCAGAGGGGAGCCCCAGCCTGTCTCAAGGCTGGGAACTGAAGGCCTGGGC T G BCAP31 Ensembl:ENSG00000185825 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:153706124..153706213;chrX:153706124..153706225 26863196 MeRIP-seq:(Medium) rs1387537968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931303,Human_RBP_ID_9443566,Human_RBP_ID_18468347 RMVar_hsa_circ_100880,RMVar_hsa_circ_108379,RMVar_hsa_circ_91406,RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264211,RMVar_hsa_circ_264213,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215,RMVar_hsa_circ_264212 96933 RMVar_ID_96933 Human_SNP_ID_735856587 m1A Human chrX - 153706753 153706753 153706753 TCCAAGGCGGTTTGCCTGCCCACCACTACAGCAGGGGCTACACGAGGTGGTCAGGTCAGGCAGGA TCCAAGGCGGTTTGCCTGCCCACCACTACAGCCGGGGCTACACGAGGTGGTCAGGTCAGGCAGGA T G BCAP31 Ensembl:ENSG00000185825 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153706749..153707117 26863196 MeRIP-seq:(Medium) rs1222187778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100880,RMVar_hsa_circ_108379,RMVar_hsa_circ_91406,RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264211,RMVar_hsa_circ_264213,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215,RMVar_hsa_circ_264212 96934 RMVar_ID_96934 Human_SNP_ID_735856603 m1A Human chrX - 153706857 153706857 153706857 CAGATAGGGAGGAGGCGCCAGCAGTGGGGATGATGGTGGGCATGTTTGCAGTTGACATGGAAAGT CAGATAGGGAGGAGGCGCCAGCAGTGGGGATGGTGGTGGGCATGTTTGCAGTTGACATGGAAAGT T C BCAP31 Ensembl:ENSG00000185825 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153706853..153707141 26863196 MeRIP-seq:(Medium) rs140064313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100880,RMVar_hsa_circ_108379,RMVar_hsa_circ_91406,RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264211,RMVar_hsa_circ_264213,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215,RMVar_hsa_circ_264212 96935 RMVar_ID_96935 Human_SNP_ID_735860035 m1A Human chrX + 153723704 153723703 153723704 TCCCTTCCCCGCCAGGCAGAACTCAGCCGCAGAGGCGGGCGCTCTGCGGGCCCAAATCCCCGCTA TCCCTTCCCCGCCAGGCAGAACTCAGCCGCAG_GGCGGGCGCTCTGCGGGCCCAAATCCCCGCTA GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153723702..153724063 26863196 MeRIP-seq:(Medium) rs1557051636 Functional Loss DEL dbSNP153 33..33 33 - - - 96936 RMVar_ID_96936 Human_SNP_ID_735860041 m1A Human chrX + 153723726 153723726 153723726 TCAGCCGCAGAGGCGGGCGCTCTGCGGGCCCAAATCCCCGCTACCAGGCAGGCCCAAGGCCGCAC TCAGCCGCAGAGGCGGGCGCTCTGCGGGCCCACATCCCCGCTACCAGGCAGGCCCAAGGCCGCAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153723722..153724056 26863196 MeRIP-seq:(Medium) rs781783249 Functional Loss SNV dbSNP153 33..33 33 - - - 96937 RMVar_ID_96937 Human_SNP_ID_735860042 m1A Human chrX + 153723726 153723726 153723726 TCAGCCGCAGAGGCGGGCGCTCTGCGGGCCCAAATCCCCGCTACCAGGCAGGCCCAAGGCCGCAC TCAGCCGCAGAGGCGGGCGCTCTGCGGGCCCATATCCCCGCTACCAGGCAGGCCCAAGGCCGCAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153723722..153724056 26863196 MeRIP-seq:(Medium) rs781783249 Functional Loss SNV dbSNP153 33..33 33 - - - 96938 RMVar_ID_96938 Human_SNP_ID_735860170 m1A Human chrX - 153724177 153724177 153724177 TACCTGCGTGTGAGAGGCAGGGGCGAGGGGAAACCGGGCGGCGCCTCTAGAAGCTGGTCTCGGGG TACCTGCGTGTGAGAGGCAGGGGCGAGGGGAAGCCGGGCGGCGCCTCTAGAAGCTGGTCTCGGGG T C BCAP31 Ensembl:ENSG00000185825 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153724172..153724425 26863196 MeRIP-seq:(Medium) rs1457110709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95586,RMVar_hsa_circ_86102,RMVar_hsa_circ_264214,RMVar_hsa_circ_264215 96939 RMVar_ID_96939 Human_SNP_ID_735860395 m1A Human chrX + 153724926 153724926 153724926 CCTGGTGCCCCGGGGAGGGGCGCCACCGGGGGAGGAGGAGGAGGAGAAGGTGGAGAGGAAGAGAC CCTGGTGCCCCGGGGAGGGGCGCCACCGGGGGGGGAGGAGGAGGAGAAGGTGGAGAGGAAGAGAC A G ABCD1 Ensembl:ENSG00000101986 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:153724876..153725075;chrX:153724875..153725075;chrX:153724875..153725036 26863196 MeRIP-seq:(Medium) rs1268737081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800421,Human_RBP_ID_5075954,Human_RBP_ID_18427893 96940 RMVar_ID_96940 Human_SNP_ID_735860626 m1A Human chrX + 153725699 153725699 153725699 TGCTGCAGTGGCTCCTCATCGCCCTCCCTGCTACCTTCGTCAACAGTGCCATCCGTTACCTGGAG TGCTGCAGTGGCTCCTCATCGCCCTCCCTGCTGCCTTCGTCAACAGTGCCATCCGTTACCTGGAG A G ABCD1 Ensembl:ENSG00000101986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153725649..153725824 26863196 MeRIP-seq:(Medium) rs1292006620 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_574 96941 RMVar_ID_96941 Human_SNP_ID_735860804 m1A Human chrX + 153726132 153726132 153726132 GCTGCGCTACATGCACTCGCGTGTGGTGGCCAACTCGGAGGAGATCGCCTTCTATGGGGGCCATG GCTGCGCTACATGCACTCGCGTGTGGTGGCCACCTCGGAGGAGATCGCCTTCTATGGGGGCCATG A C ABCD1 Ensembl:ENSG00000101986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153726082..153726322 26863196 MeRIP-seq:(Medium) rs782346129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2244891,Human_Splice_Rec_2244908 96942 RMVar_ID_96942 Human_SNP_ID_735860805 m1A Human chrX + 153726132 153726132 153726132 GCTGCGCTACATGCACTCGCGTGTGGTGGCCAACTCGGAGGAGATCGCCTTCTATGGGGGCCATG GCTGCGCTACATGCACTCGCGTGTGGTGGCCAGCTCGGAGGAGATCGCCTTCTATGGGGGCCATG A G ABCD1 Ensembl:ENSG00000101986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153726082..153726322 26863196 MeRIP-seq:(Medium) rs782346129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2244891,Human_Splice_Rec_2244908 96943 RMVar_ID_96943 Human_SNP_ID_735863338 m1A Human chrX + 153737927 153737927 153737927 GGGGGTGGTGGGGGTGGGATGAAGCCTTGCCCAGGAGTTGCTGTGAGCGAGTGGGCAGGCAGCTG GGGGGTGGTGGGGGTGGGATGAAGCCTTGCCCGGGAGTTGCTGTGAGCGAGTGGGCAGGCAGCTG A G ABCD1 Ensembl:ENSG00000101986 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153737925..153738025 26863196 MeRIP-seq:(Medium) rs1200047796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93695,RMVar_hsa_circ_264217 96944 RMVar_ID_96944 Human_SNP_ID_735863812 m1A Human chrX - 153740224 153740224 153740224 GGCGCACGGGCTTCCTTACCTCTGCGGGATGTAGAACATGCGCTGGGGTGGGGGCTTGTAGAGCA GGCGCACGGGCTTCCTTACCTCTGCGGGATGTGGAACATGCGCTGGGGTGGGGGCTTGTAGAGCA T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153740174..153740661 32194978 MeRIP-seq:(Medium) rs1569541094 Functional Loss SNV dbSNP153 33..33 33 - - - 96945 RMVar_ID_96945 Human_SNP_ID_735864744 m1A Human chrX - 153743771 153743771 153743771 GGTGGGTGCTGCTGTCTCCTTCATGTGATCCGAGCTTGGGGGCGGGGCAGGGGCCGGGGACGGTT GGTGGGTGCTGCTGTCTCCTTCATGTGATCCGCGCTTGGGGGCGGGGCAGGGGCCGGGGACGGTT T G U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153743721..153743865 26863196 MeRIP-seq:(Medium) rs1201481584 Functional Loss SNV dbSNP153 33..33 33 - - - 96946 RMVar_ID_96946 Human_SNP_ID_735868697 m1A Human chrX - 153763324 153763324 153763324 CTGAGGGGCCCATGAGGGAGGAGGAAATGGTGATGGGGCTGGGGAGGCCTGGGGGTGAGAAGCTT CTGAGGGGCCCATGAGGGAGGAGGAAATGGTGGTGGGGCTGGGGAGGCCTGGGGGTGAGAAGCTT T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153763319..153763417 26863196 MeRIP-seq:(Medium) rs893928935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931304,Human_RBP_ID_5330872,Human_RBP_ID_9443377 96947 RMVar_ID_96947 Human_SNP_ID_735869464 m1A Human chrX + 153766418 153766418 153766418 ACTTAGATCTCTCTTGTCTGGGTGGTGGGCGCAGGGGCGCGCTGTGACACAGCTTCCGCCAGCCT ACTTAGATCTCTCTTGTCTGGGTGGTGGGCGCGGGGGCGCGCTGTGACACAGCTTCCGCCAGCCT A G PLXNB3 Ensembl:ENSG00000198753 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153766368..153767047 26863196 MeRIP-seq:(Medium) rs1465950834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18963722,Human_RBP_ID_21997336 RMVar_hsa_circ_75542,RMVar_hsa_circ_98116,RMVar_hsa_circ_264219,RMVar_hsa_circ_264220 96948 RMVar_ID_96948 Human_SNP_ID_735870425 m1A Human chrX + 153769173 153769173 153769173 TCTGCTCTGCTGCCCCTCCAGGTGGACCGGATACCTGTGGCAGCCTGCCCCCAGTTCCCTGACTG TCTGCTCTGCTGCCCCTCCAGGTGGACCGGATGCCTGTGGCAGCCTGCCCCCAGTTCCCTGACTG A G PLXNB3 Ensembl:ENSG00000198753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153768362..153770111 32194978 MeRIP-seq:(Medium) rs1557060605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967624 Human_Splice_Rec_2244936,Human_Splice_Rec_2244937,Human_Splice_Rec_2245006,Human_Splice_Rec_2245007 RMVar_hsa_circ_75542,RMVar_hsa_circ_98116,RMVar_hsa_circ_264219,RMVar_hsa_circ_264220 96949 RMVar_ID_96949 Human_SNP_ID_735873597 m1A Human chrX + 153777355 153777355 153777355 GCCAGCAAGGGCCAAGGCCATTCCGGAAATCTACCTCACCCGTCTGCTGTCCATGAAGGTTGGTG GCCAGCAAGGGCCAAGGCCATTCCGGAAATCTGCCTCACCCGTCTGCTGTCCATGAAGGTTGGTG A G PLXNB3,SRPK3 Ensembl:ENSG00000198753,Ensembl:ENSG00000184343 Protein coding,Protein coding CDS,5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153777304..153777540 32194978 MeRIP-seq:(Medium) rs781902036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2244985,Human_Splice_Rec_2245055,Human_Splice_Rec_2245090,Human_Splice_Rec_2245108 Human_miRNA_ID_1915471,Human_miRNA_ID_1917920,Human_miRNA_ID_1920374,Human_miRNA_ID_1922832,Human_miRNA_ID_1925285,Human_miRNA_ID_1927736,Human_miRNA_ID_1930187,Human_miRNA_ID_1932634,Human_miRNA_ID_2008041,Human_miRNA_ID_2630462,Human_miRNA_ID_2643577,Human_miRNA_ID_2710283,Human_miRNA_ID_3126320 RMVar_hsa_circ_88479,RMVar_hsa_circ_98116,RMVar_hsa_circ_264220,RMVar_hsa_circ_264221 96950 RMVar_ID_96950 Human_SNP_ID_735874340 m1A Human chrX - 153779740 153779740 153779740 GGGTACCTGATGGCCTCTCTTTGTCTGTGGGTAGCAGGTTATAGGCATGGGGCTGAGGGACTCTC GGGTACCTGATGGCCTCTCTTTGTCTGTGGGTTGCAGGTTATAGGCATGGGGCTGAGGGACTCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153779734..153779911 26863196 MeRIP-seq:(Medium) rs1325967775 Functional Loss SNV dbSNP153 33..33 33 - - - 96951 RMVar_ID_96951 Human_SNP_ID_735874341 m1A Human chrX - 153779740 153779740 153779740 GGGTACCTGATGGCCTCTCTTTGTCTGTGGGTAGCAGGTTATAGGCATGGGGCTGAGGGACTCTC GGGTACCTGATGGCCTCTCTTTGTCTGTGGGTGGCAGGTTATAGGCATGGGGCTGAGGGACTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153779734..153779911 26863196 MeRIP-seq:(Medium) rs1325967775 Functional Loss SNV dbSNP153 33..33 33 - - - 96952 RMVar_ID_96952 Human_SNP_ID_735876395 m1A Human chrX + 153785863 153785863 153785863 GGGGAATCCAAGGAGCAAACCAAGAAGGTCCTAGGGCCAGCCTAGGCCTCCACGGCCCGGCCGTT GGGGAATCCAAGGAGCAAACCAAGAAGGTCCTGGGGCCAGCCTAGGCCTCCACGGCCCGGCCGTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153785814..153785914 32194978 MeRIP-seq:(Medium) rs1464860671 Functional Loss SNV dbSNP153 33..33 33 - - - 96953 RMVar_ID_96953 Human_SNP_ID_735876677 m1A Human chrX + 153786820 153786820 153786820 CACCGGCACTCACTGTTTCAAACACCGCGTACACATGGCCATAGTTGGCCCCAGCCACAAGGCCT CACCGGCACTCACTGTTTCAAACACCGCGTACGCATGGCCATAGTTGGCCCCAGCCACAAGGCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153786358..153786907 32194978 MeRIP-seq:(Medium) rs781931147 Functional Loss SNV dbSNP153 33..33 33 - - - 96954 RMVar_ID_96954 Human_SNP_ID_735876849 m1A Human chrX - 153787533 153787533 153787533 CATCACCAAGGCCAAGTCCCTGCGCATTGCCGAGTATGCCTTCAAGCTGGCGCAGGAGAGCGGGC CATCACCAAGGCCAAGTCCCTGCGCATTGCCGCGTATGCCTTCAAGCTGGCGCAGGAGAGCGGGC T G IDH3G Ensembl:ENSG00000067829 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153787485..153787620 26863196 MeRIP-seq:(Medium) rs782072420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967628,Human_RBP_ID_19026963,Human_RBP_ID_26363478,Human_RBP_ID_26835798 Human_Splice_Rec_2245312,Human_Splice_Rec_2245313,Human_Splice_Rec_2245320,Human_Splice_Rec_2245343,Human_Splice_Rec_2245344,Human_Splice_Rec_2245363,Human_Splice_Rec_2245364,Human_Splice_Rec_2245385,Human_Splice_Rec_2245386,Human_Splice_Rec_2245404,Human_Splice_Rec_2245405,Human_Splice_Rec_2245426,Human_Splice_Rec_2245427,Human_Splice_Rec_2245436,Human_Splice_Rec_2245437,Human_Splice_Rec_2245452,Human_Splice_Rec_2245453,Human_Splice_Rec_2245468 Human_miRNA_ID_2933301 RMVar_hsa_circ_94526,RMVar_hsa_circ_264224 96955 RMVar_ID_96955 Human_SNP_ID_735876910 m1A Human chrX - 153787790 153787790 153787790 GTGTGCATGGGGGGCCCGAGATGAGCCCCCCCAGCGTCAAGATTAAGGGGAGAGCTTAAGGAACC GTGTGCATGGGGGGCCCGAGATGAGCCCCCCCGGCGTCAAGATTAAGGGGAGAGCTTAAGGAACC T C IDH3G Ensembl:ENSG00000067829 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153787785..153787998 26863196 MeRIP-seq:(Medium) rs782291712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5411515 RMVar_hsa_circ_94526,RMVar_hsa_circ_264224 96956 RMVar_ID_96956 Human_SNP_ID_735876944 m1A Human chrX + 153787899 153787897 153787900 CAATGAGGATGTCTATGTCCTTGTGCCGGGTCACCACGCCTGGAAGGCTCTTACAGTGGATGACG CAATGAGGATGTCTATGTCCTTGTGCCGGGT___CACGCCTGGAAGGCTCTTACAGTGGATGACG TCAC T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153787851..153787900 32194978 MeRIP-seq:(Medium) rs782384807 Functional Loss DEL dbSNP153 32..34 33 - - - 96957 RMVar_ID_96957 Human_SNP_ID_735878507 m1A Human chrX - 153794742 153794742 153794742 AGCCCCGGCTGGGCCGCTACCTGAGCAGCGGGAGAGGCTGGACAGCAGGAGCAGCGCCAGGGCGC AGCCCCGGCTGGGCCGCTACCTGAGCAGCGGGTGAGGCTGGACAGCAGGAGCAGCGCCAGGGCGC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153794676..153794816 32194978 MeRIP-seq:(Medium) rs781824791 Functional Loss SNV dbSNP153 33..33 33 - - - 96958 RMVar_ID_96958 Human_SNP_ID_735878893 m1A Human chrX - 153796483 153796483 153796483 ATGAAGACGGTCTCAGTGGAAATGACAGCGTCAGAAGTGGTGTAGTAGGAAGGGGTGATCTGGGG ATGAAGACGGTCTCAGTGGAAATGACAGCGTCGGAAGTGGTGTAGTAGGAAGGGGTGATCTGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:153796382..153796588;chrX:153796426..153796507 26863196 MeRIP-seq:(Medium) rs782400120 Functional Loss SNV dbSNP153 33..33 33 - - - 96959 RMVar_ID_96959 Human_SNP_ID_735879128 m1A Human chrX + 153797508 153797508 153797508 GACGTCGGTGGAAAACAATTCCCTGTCACTCGAGGCCAGGATGTGGGGCGTTATCAGGTGAGGGG GACGTCGGTGGAAAACAATTCCCTGTCACTCGGGGCCAGGATGTGGGGCGTTATCAGGTGAGGGG A G SSR4 Ensembl:ENSG00000180879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153797425..153797568 26863196 MeRIP-seq:(Medium) rs782463420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257571,Human_RBP_ID_731191,Human_RBP_ID_799821,Human_RBP_ID_849008,Human_RBP_ID_967630,Human_RBP_ID_17325471,Human_RBP_ID_18197398,Human_RBP_ID_18472965,Human_RBP_ID_19027765,Human_RBP_ID_22467796,Human_RBP_ID_22777808,Human_RBP_ID_26835135 Human_Splice_Rec_2245492,Human_Splice_Rec_2245493,Human_Splice_Rec_2245508,Human_Splice_Rec_2245509,Human_Splice_Rec_2245519,Human_Splice_Rec_2245526,Human_Splice_Rec_2245527,Human_Splice_Rec_2245534,Human_Splice_Rec_2245535,Human_Splice_Rec_2245554,Human_Splice_Rec_2245560,Human_Splice_Rec_2245561,Human_Splice_Rec_2245570,Human_Splice_Rec_2245571,Human_Splice_Rec_2245578 RMVar_hsa_circ_294615,RMVar_hsa_circ_119882,RMVar_hsa_circ_264229,RMVar_hsa_circ_264230 96960 RMVar_ID_96960 Human_SNP_ID_735881230 m1A Human chrX + 153805151 153805151 153805151 AGTTTACGAGCACGCAGCTCCCCCTCATTCTCAGAGCCAAAGTCATCCAGGAAGTCATCCCGGTC AGTTTACGAGCACGCAGCTCCCCCTCATTCTCTGAGCCAAAGTCATCCAGGAAGTCATCCCGGTC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153802814..153805175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 96961 RMVar_ID_96961 Human_SNP_ID_735882085 m1A Human chrX - 153808592 153808592 153808592 GTTCTTACGGAGGCGTGTCTCTGCCGCAGGTGAACGGGAAGGAGCTCTCCAAGCTGTCTCAGGAG GTTCTTACGGAGGCGTGTCTCTGCCGCAGGTGGACGGGAAGGAGCTCTCCAAGCTGTCTCAGGAG T C PDZD4 Ensembl:ENSG00000067840 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153808087..153829589 32194978 MeRIP-seq:(Medium) rs1286489839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2245589,Human_Splice_Rec_2245613,Human_Splice_Rec_2245639,Human_Splice_Rec_2245651,Human_Splice_Rec_2245668,Human_Splice_Rec_2245678 96962 RMVar_ID_96962 Human_SNP_ID_735885948 m1A Human chrX + 153830433 153830433 153830433 CCTGGCGCGGGGGGCGGGCCGCCTAGCGGGGGAGGGGGGCACGCCCCCGAGGTGGGGGCAGCGGC CCTGGCGCGGGGGGCGGGCCGCCTAGCGGGGGGGGGGGGCACGCCCCCGAGGTGGGGGCAGCGGC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:153830416..153830543 26863196 MeRIP-seq:(Medium) rs868924861 Functional Loss SNV dbSNP153 33..33 33 - - - 96963 RMVar_ID_96963 Human_SNP_ID_735885949 m1A Human chrX + 153830433 153830433 153830433 CCTGGCGCGGGGGGCGGGCCGCCTAGCGGGGGAGGGGGGCACGCCCCCGAGGTGGGGGCAGCGGC CCTGGCGCGGGGGGCGGGCCGCCTAGCGGGGGTGGGGGGCACGCCCCCGAGGTGGGGGCAGCGGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:153830416..153830543 26863196 MeRIP-seq:(Medium) rs868924861 Functional Loss SNV dbSNP153 33..33 33 - - - 96964 RMVar_ID_96964 Human_SNP_ID_735892107 m1A Human chrX + 153861980 153861980 153861980 TGGGAGGAGGTGTGCCCGCCCCGCAGCCAGGTAGTGACGGAGGCCACTTGGATGTTGTGTGGTGG TGGGAGGAGGTGTGCCCGCCCCGCAGCCAGGTGGTGACGGAGGCCACTTGGATGTTGTGTGGTGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:153861776..153862209 26863196 MeRIP-seq:(Medium) rs1557088945 Functional Loss SNV dbSNP153 33..33 33 - - - 96965 RMVar_ID_96965 Human_SNP_ID_735892790 m1A Human chrX - 153864684 153864684 153864684 GCATCCCCCCAGGGATCTCAGATTTTGGCAACATCTCAGCCACAGCGGGTGAAAACTACAGTGTC GCATCCCCCCAGGGATCTCAGATTTTGGCAACTTCTCAGCCACAGCGGGTGAAAACTACAGTGTC T A L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:153864676..153864700 26863196 MeRIP-seq:(Medium) rs916189296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2245724,Human_Splice_Rec_2245725,Human_Splice_Rec_2245778,Human_Splice_Rec_2245779,Human_Splice_Rec_2245832,Human_Splice_Rec_2245833,Human_Splice_Rec_2245888,Human_Splice_Rec_2245889 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_9720 96966 RMVar_ID_96966 Human_SNP_ID_735892874 m1A Human chrX - 153864961 153864961 153864961 GGATGAGGGGGGCAAGGGGCAACTGTCCTTCAACCTTCGGGACCCCGAACTTCGGACACACAACC GGATGAGGGGGGCAAGGGGCAACTGTCCTTCAGCCTTCGGGACCCCGAACTTCGGACACACAACC T C L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153864813..153864997 26863196 MeRIP-seq:(Medium) rs782781265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94509,Human_RBP_ID_27550442 Human_Splice_Rec_2245722,Human_Splice_Rec_2245776,Human_Splice_Rec_2245830,Human_Splice_Rec_2245886,Human_Splice_Rec_2245906 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_9720 96967 RMVar_ID_96967 Human_SNP_ID_735892941 m1A Human chrX - 153865144 153865144 153865144 CCAGTCGAACACCAGCCTGCTGCTGCGCTGGCAGCCCCCACTCAGCCACAACGGCGTGCTCACCG CCAGTCGAACACCAGCCTGCTGCTGCGCTGGCTGCCCCCACTCAGCCACAACGGCGTGCTCACCG T A L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153865093..153865162 26863196 MeRIP-seq:(Medium) rs782566102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22778645 Human_Splice_Rec_2245720,Human_Splice_Rec_2245721,Human_Splice_Rec_2245774,Human_Splice_Rec_2245775,Human_Splice_Rec_2245828,Human_Splice_Rec_2245829,Human_Splice_Rec_2245884,Human_Splice_Rec_2245885,Human_Splice_Rec_2245904,Human_Splice_Rec_2245905 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_9720 96968 RMVar_ID_96968 Human_SNP_ID_735893022 m1A Human chrX - 153865473 153865473 153865473 TGCAGGTGACGTACTGGAGGGAGGGCAGTCAGAGGAAGCACAGCAAGAGACATATCCACAAAGAC TGCAGGTGACGTACTGGAGGGAGGGCAGTCAGTGGAAGCACAGCAAGAGACATATCCACAAAGAC T A L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:153865384..153865525;chrX:153865384..153865542 26863196 MeRIP-seq:(Medium) rs782357988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2245718,Human_Splice_Rec_2245772,Human_Splice_Rec_2245826,Human_Splice_Rec_2245882,Human_Splice_Rec_2245902 Human_miRNA_ID_2237999 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098,RMVar_hsa_circ_9720 96969 RMVar_ID_96969 Human_SNP_ID_735893075 m1A Human chrX - 153865692 153865692 153865692 GGCCACCTCCGCGGATACAATGTAAGGGTTGAAGGCATGGGGGCCCAGGAGGGTGATCACTGAGG GGCCACCTCCGCGGATACAATGTAAGGGTTGAGGGCATGGGGGCCCAGGAGGGTGATCACTGAGG T C L1CAM Ensembl:ENSG00000198910 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153865690..153865762 26863196 MeRIP-seq:(Medium) rs782290004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098 96970 RMVar_ID_96970 Human_SNP_ID_735893080 m1A Human chrX - 153865705 153865705 153865705 GGCCCAGGTCAAGGGCCACCTCCGCGGATACAATGTAAGGGTTGAAGGCATGGGGGCCCAGGAGG GGCCCAGGTCAAGGGCCACCTCCGCGGATACAGTGTAAGGGTTGAAGGCATGGGGGCCCAGGAGG T C L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153865701..153865725 26863196 MeRIP-seq:(Medium) rs139621907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2245717,Human_Splice_Rec_2245771,Human_Splice_Rec_2245825,Human_Splice_Rec_2245881,Human_Splice_Rec_2245901 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098 96971 RMVar_ID_96971 Human_SNP_ID_735893277 m1A Human chrX - 153866714 153866714 153866714 GTCCACCTTCGTGCCCTATGAGATCAAAGTCCAGGCCGTCAACAGCCAGGGCAAGGGACCAGAGC GTCCACCTTCGTGCCCTATGAGATCAAAGTCCGGGCCGTCAACAGCCAGGGCAAGGGACCAGAGC T C L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:153866651..153866725 26863196 MeRIP-seq:(Medium) rs1557090981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94514,Human_RBP_ID_967871 Human_Splice_Rec_2245715,Human_Splice_Rec_2245769,Human_Splice_Rec_2245823,Human_Splice_Rec_2245879 Human_miRNA_ID_2333825,Human_miRNA_ID_2510093,Human_miRNA_ID_2542819,Human_miRNA_ID_2544682,Human_miRNA_ID_2546519,Human_miRNA_ID_2548387,Human_miRNA_ID_2550250,Human_miRNA_ID_2552120,Human_miRNA_ID_2557534,Human_miRNA_ID_2559419,Human_miRNA_ID_2589832,Human_miRNA_ID_2966910,Human_miRNA_ID_3091539 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098,RMVar_hsa_circ_264236 96972 RMVar_ID_96972 Human_SNP_ID_735893317 m1A Human chrX - 153866831 153866831 153866831 GTGGATGGACTGGAACGCCCCCCAGGTTCAGTACCGCGTGCAGTGGCGCCCTCAGGGGACACGAG GTGGATGGACTGGAACGCCCCCCAGGTTCAGTCCCGCGTGCAGTGGCGCCCTCAGGGGACACGAG T G L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153866625..153866870 26863196 MeRIP-seq:(Medium) rs1064794855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22778382 Human_Splice_Rec_2245714,Human_Splice_Rec_2245768,Human_Splice_Rec_2245822,Human_Splice_Rec_2245878,Human_Splice_Rec_2245914 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098,RMVar_hsa_circ_264236 96973 RMVar_ID_96973 Human_SNP_ID_735893482 m1A Human chrX - 153867524 153867524 153867524 CAGAATATGACATTGAATTTGAGGACAAGGAAATGGCGCCTGAAAAATGGTACAGTCTGGGCAAG CAGAATATGACATTGAATTTGAGGACAAGGAAGTGGCGCCTGAAAAATGGTACAGTCTGGGCAAG T C L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:153867476..153867525 26863196 MeRIP-seq:(Medium) rs1557091406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94517,Human_RBP_ID_27550445 Human_Splice_Rec_2245710,Human_Splice_Rec_2245764,Human_Splice_Rec_2245818,Human_Splice_Rec_2245874,Human_Splice_Rec_2245910,Human_Splice_Rec_2245920 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_264233,RMVar_hsa_circ_467,RMVar_hsa_circ_97138,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098 96974 RMVar_ID_96974 Human_SNP_ID_735893607 m1A Human chrX - 153867980 153867980 153867980 AGCTCTTGGTGGTGGGTAAGTCCTAGGGTGGAAGCCTCCACTCCAGAAGGCCGGGGCTCACATCC AGCTCTTGGTGGTGGGTAAGTCCTAGGGTGGAGGCCTCCACTCCAGAAGGCCGGGGCTCACATCC T C L1CAM Ensembl:ENSG00000198910 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:153867976..153868000;chrX:153867976..153868025 26863196 MeRIP-seq:(Medium) rs782256440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_467,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098 96975 RMVar_ID_96975 Human_SNP_ID_735897177 m1A Human chrX + 153883735 153883702 153883736 CCTGGCAGACCAGGGTCTTGGCTGGGATCCCCATCCTGGCAGACCTCCTCACAGGACCCCACCAC __________________________________CCTGGCAGACCTCCTCACAGGACCCCACCAC GCCTGGCAGACCAGGGTCTTGGCTGGGATCCCCAT G U52112.1 Ensembl:ENSG00000273769 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153883730..153883914 26863196 MeRIP-seq:(Medium) rs1193531906 Functional Loss DEL dbSNP153 1..34 33 - - - Human_Splice_Rec_2245982 96976 RMVar_ID_96976 Human_SNP_ID_735907678 m1A Human chrX - 153928159 153928159 153928159 CGCGGCGCCCTCCTTCCGCCCCGGCCAGGCCCATGGGACCCGGCCCGCCCTCTGCCGTCCGTCCC CGCGGCGCCCTCCTTCCGCCCCGGCCAGGCCCTTGGGACCCGGCCCGCCCTCTGCCGTCCGTCCC T A ARHGAP4 Ensembl:ENSG00000089820 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:153928090..153928218 26863410 MeRIP-seq:(Medium) rs1377597321 Functional Loss SNV dbSNP153 33..33 33 - - - 96977 RMVar_ID_96977 Human_SNP_ID_735907679 m1A Human chrX - 153928159 153928159 153928159 CGCGGCGCCCTCCTTCCGCCCCGGCCAGGCCCATGGGACCCGGCCCGCCCTCTGCCGTCCGTCCC CGCGGCGCCCTCCTTCCGCCCCGGCCAGGCCCCTGGGACCCGGCCCGCCCTCTGCCGTCCGTCCC T G ARHGAP4 Ensembl:ENSG00000089820 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:153928090..153928218 26863410 MeRIP-seq:(Medium) rs1377597321 Functional Loss SNV dbSNP153 33..33 33 - - - 96978 RMVar_ID_96978 Human_SNP_ID_735908166 m1A Human chrX - 153930220 153930220 153930220 CCCGCTTCTCCCTGGGTTCCTGGTGGCAGCTGAGGCGGCACCTGGAGCTGAAAGAGAAGGGCAGG CCCGCTTCTCCCTGGGTTCCTGGTGGCAGCTGTGGCGGCACCTGGAGCTGAAAGAGAAGGGCAGG T A NAA10,ARHGAP4 Ensembl:ENSG00000102030,Ensembl:ENSG00000089820 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153929901..153930290 26863196 MeRIP-seq:(Medium) rs781848505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257001,Human_RBP_ID_731250,Human_RBP_ID_848759,Human_RBP_ID_967631,Human_RBP_ID_5056294,Human_RBP_ID_5124813,Human_RBP_ID_18173775,Human_RBP_ID_19027766,Human_RBP_ID_19150728,Human_RBP_ID_22122987 Human_Splice_Rec_2246488,Human_Splice_Rec_2246490,Human_Splice_Rec_2246504,Human_Splice_Rec_2246518,Human_Splice_Rec_2246530,Human_Splice_Rec_2246542,Human_Splice_Rec_2246550,Human_Splice_Rec_2246560,Human_Splice_Rec_2246572 RMVar_hsa_circ_264246,RMVar_hsa_circ_87329,RMVar_hsa_circ_116388,RMVar_hsa_circ_117427,RMVar_hsa_circ_112768,RMVar_hsa_circ_79013,RMVar_hsa_circ_264247,RMVar_hsa_circ_264244,RMVar_hsa_circ_264245,RMVar_hsa_circ_264243 96979 RMVar_ID_96979 Human_SNP_ID_735908270 m1A Human chrX - 153930693 153930693 153930693 GCGGCACTCAGGAGCCCCAAGACAGTGGCTGCAGGCGAGACCGACTTTGGATGCCAGCTCTTGTG GCGGCACTCAGGAGCCCCAAGACAGTGGCTGCGGGCGAGACCGACTTTGGATGCCAGCTCTTGTG T C NAA10,ARHGAP4 Ensembl:ENSG00000102030,Ensembl:ENSG00000089820 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153930688..153930800 32194978 MeRIP-seq:(Medium) rs1268428087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1229931,Human_RBP_ID_16846998 RMVar_hsa_circ_264246,RMVar_hsa_circ_87329,RMVar_hsa_circ_116388,RMVar_hsa_circ_117427,RMVar_hsa_circ_112768,RMVar_hsa_circ_79013,RMVar_hsa_circ_264247,RMVar_hsa_circ_264244,RMVar_hsa_circ_264245,RMVar_hsa_circ_264243 96980 RMVar_ID_96980 Human_SNP_ID_735908400 m1A Human chrX - 153931305 153931305 153931305 ATGTCTTAGGCCTGGCAGGGCCAGCCTAGGCCATTGAGTCCAGCTCCCCTTCCAGGGACATGGCC ATGTCTTAGGCCTGGCAGGGCCAGCCTAGGCCGTTGAGTCCAGCTCCCCTTCCAGGGACATGGCC T C NAA10,ARHGAP4 Ensembl:ENSG00000102030,Ensembl:ENSG00000089820 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153930719..153931868 26863196 MeRIP-seq:(Medium) rs1451390603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264246,RMVar_hsa_circ_87329,RMVar_hsa_circ_116388,RMVar_hsa_circ_117427,RMVar_hsa_circ_112768,RMVar_hsa_circ_79013,RMVar_hsa_circ_264247,RMVar_hsa_circ_264244,RMVar_hsa_circ_264245,RMVar_hsa_circ_264243,RMVar_hsa_circ_372748,RMVar_hsa_circ_264249,RMVar_hsa_circ_105316,RMVar_hsa_circ_264250 96981 RMVar_ID_96981 Human_SNP_ID_735908658 m1A Human chrX - 153932586 153932586 153932586 GCTCCTTTGCAGCCTCTCCTTTCTCCCTCTCCAGGGAAGAGGACCCAGATGATGTGCCCCATGGA GCTCCTTTGCAGCCTCTCCTTTCTCCCTCTCCGGGGAAGAGGACCCAGATGATGTGCCCCATGGA T C NAA10,ARHGAP4 Ensembl:ENSG00000102030,Ensembl:ENSG00000089820 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153932526..153932600 26863196 MeRIP-seq:(Medium) rs782725354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22692779 Human_Splice_Rec_2246383,Human_Splice_Rec_2246481,Human_Splice_Rec_2246497,Human_Splice_Rec_2246511,Human_Splice_Rec_2246525,Human_Splice_Rec_2246537,Human_Splice_Rec_2246543,Human_Splice_Rec_2246554,Human_Splice_Rec_2246567,Human_Splice_Rec_2246581,Human_Splice_Rec_2246593,Human_Splice_Rec_2246601,Human_Splice_Rec_2246607 RMVar_hsa_circ_116388,RMVar_hsa_circ_112768,RMVar_hsa_circ_79013,RMVar_hsa_circ_264244,RMVar_hsa_circ_264245,RMVar_hsa_circ_264243,RMVar_hsa_circ_123238,RMVar_hsa_circ_264252 96982 RMVar_ID_96982 Human_SNP_ID_735908996 m1A Human chrX + 153934388 153934388 153934388 CCAAATTCAGAAGCTGCCCACCTGGGGCCAGGAAAGGCCATGGTAGAAGTAGTATTTCATCTGGT CCAAATTCAGAAGCTGCCCACCTGGGGCCAGGGAAGGCCATGGTAGAAGTAGTATTTCATCTGGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153934376..153934500 32194978 MeRIP-seq:(Medium) rs387906701 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_575 GWAS_ID_12775 96983 RMVar_ID_96983 Human_SNP_ID_735909120 m1A Human chrX + 153934942 153934942 153934942 CGGCGGGGCTCGCGGGTCCCAGCGGATCGTGAAGGCGCAGTCAGCTGCCGCCGCGCTCCGAAGCG CGGCGGGGCTCGCGGGTCCCAGCGGATCGTGAGGGCGCAGTCAGCTGCCGCCGCGCTCCGAAGCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:153934876..153935000;chrX:153934775..153934975 32194978 MeRIP-seq:(Medium) rs1339748139 Functional Loss SNV dbSNP153 33..33 33 - - - 96984 RMVar_ID_96984 Human_SNP_ID_735909121 m1A Human chrX + 153934942 153934942 153934942 CGGCGGGGCTCGCGGGTCCCAGCGGATCGTGAAGGCGCAGTCAGCTGCCGCCGCGCTCCGAAGCG CGGCGGGGCTCGCGGGTCCCAGCGGATCGTGATGGCGCAGTCAGCTGCCGCCGCGCTCCGAAGCG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:153934876..153935000;chrX:153934775..153934975 32194978 MeRIP-seq:(Medium) rs1339748139 Functional Loss SNV dbSNP153 33..33 33 - - - 96985 RMVar_ID_96985 Human_SNP_ID_735909131 m1A Human chrX + 153934983 153934983 153934983 CAGCTGCCGCCGCGCTCCGAAGCGACGCCGGGACGGCCGGGGCTGGGACCGGAGCTGGGCTCGCT CAGCTGCCGCCGCGCTCCGAAGCGACGCCGGGCCGGCCGGGGCTGGGACCGGAGCTGGGCTCGCT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:153934875..153935025;chrX:153934775..153935173;chrX:153934725..153935050;chrX:153934401..153935050 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1191601583 Functional Loss SNV dbSNP153 33..33 33 - - - 96986 RMVar_ID_96986 Human_SNP_ID_735909137 m1A Human chrX + 153935003 153934991 153935003 AGCGACGCCGGGACGGCCGGGGCTGGGACCGGAGCTGGGCTCGCTGGGCGACGGCGGAAGGGGCG AGCGACGCCGGGACGGCCGGG____________GCTGGGCTCGCTGGGCGACGGCGGAAGGGGCG GGCTGGGACCGGA G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrX:153934909..153935019 26863410 MeRIP-seq:(Medium) rs1569546335 Functional Loss DEL dbSNP153 22..33 33 - - - 96987 RMVar_ID_96987 Human_SNP_ID_735912655 m1A Human chrX - 153949611 153949611 153949611 CTCACGCATCTCTCCCGTTCCTTCCAGAAACCAGTAAAGACAGCTCTGGCACCAAGCCAGCCAAC CTCACGCATCTCTCCCGTTCCTTCCAGAAACCGGTAAAGACAGCTCTGGCACCAAGCCAGCCAAC T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153949529..153949633 26863196 MeRIP-seq:(Medium) rs1357538753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16847350 Human_Splice_Rec_2246736,Human_Splice_Rec_2246737,Human_Splice_Rec_2246786,Human_Splice_Rec_2246787,Human_Splice_Rec_2246836,Human_Splice_Rec_2246837 RMVar_hsa_circ_106656,RMVar_hsa_circ_122094,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_1652,RMVar_hsa_circ_264255,RMVar_hsa_circ_264259,RMVar_hsa_circ_90706,RMVar_hsa_circ_98909,RMVar_hsa_circ_75687,RMVar_hsa_circ_264260,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_264262 96988 RMVar_ID_96988 Human_SNP_ID_735913467 m1A Human chrX - 153952780 153952780 153952780 TCTGAGCAGCACAGGGGAGCCATCTTCGGGCCAGGAGTCTGCCGGCTCTGCGGTGGTGGCCACTG TCTGAGCAGCACAGGGGAGCCATCTTCGGGCCGGGAGTCTGCCGGCTCTGCGGTGGTGGCCACTG T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153952733..153952933 32194978 MeRIP-seq:(Medium) rs1323826708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257532,Human_RBP_ID_7986818,Human_RBP_ID_8162674,Human_RBP_ID_8933657,Human_RBP_ID_9318105,Human_RBP_ID_18917162 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_127722,RMVar_hsa_circ_264266,RMVar_hsa_circ_70497,RMVar_hsa_circ_264265 96989 RMVar_ID_96989 Human_SNP_ID_735913766 m1A Human chrX - 153953753 153953753 153953753 CTGTCGCCCCCACAGACCCCCCACCTGCTGCCAGCGATCAGGGAGAGGTGGAGAGCACCCAGGGC CTGTCGCCCCCACAGACCCCCCACCTGCTGCCGGCGATCAGGGAGAGGTGGAGAGCACCCAGGGC T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153953702..153953772 26863196 MeRIP-seq:(Medium) rs782204229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7986824,Human_RBP_ID_8938895,Human_RBP_ID_9317637,Human_RBP_ID_17328199 Human_Splice_Rec_2246722,Human_Splice_Rec_2246772,Human_Splice_Rec_2246822 Human_miRNA_ID_3002421 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_70497,RMVar_hsa_circ_264267 96990 RMVar_ID_96990 Human_SNP_ID_735913770 m1A Human chrX - 153953770 153953770 153953770 GCTGAGCAGCCGCCTGCCTGTCGCCCCCACAGACCCCCCACCTGCTGCCAGCGATCAGGGAGAGG GCTGAGCAGCCGCCTGCCTGTCGCCCCCACAGGCCCCCCACCTGCTGCCAGCGATCAGGGAGAGG T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153953649..153953793 26863196 MeRIP-seq:(Medium) rs782122807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9317637 Human_Splice_Rec_2246722,Human_Splice_Rec_2246772,Human_Splice_Rec_2246822 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_70497,RMVar_hsa_circ_264267 96991 RMVar_ID_96991 Human_SNP_ID_735914030 m1A Human chrX - 153954483 153954483 153954483 AGACCCACGAGACAGGCACCACCAACACCGCCACTACCTCGAATGCAGGCAGCGCCCAGAGGGTG AGACCCACGAGACAGGCACCACCAACACCGCCGCTACCTCGAATGCAGGCAGCGCCCAGAGGGTG T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153954434..153954603 26863196 MeRIP-seq:(Medium) rs1343470916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1071039,Human_RBP_ID_8933688,Human_RBP_ID_9265412,Human_RBP_ID_9317641,Human_RBP_ID_21765256,Human_RBP_ID_27380254,Human_RBP_ID_27550507 Human_miRNA_ID_1915472,Human_miRNA_ID_1917921,Human_miRNA_ID_1920375,Human_miRNA_ID_1922833,Human_miRNA_ID_1925286,Human_miRNA_ID_1927737,Human_miRNA_ID_1930188,Human_miRNA_ID_1932635,Human_miRNA_ID_2169046,Human_miRNA_ID_2170569,Human_miRNA_ID_2630463,Human_miRNA_ID_2643578,Human_miRNA_ID_3126321 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_264267 96992 RMVar_ID_96992 Human_SNP_ID_735914269 m1A Human chrX - 153955078 153955078 153955078 AACATGGCCGGGCAGCATGGCTGCTCAAACCCACCCTGCGAGACCCACGAGACGGGCACCACCAA AACATGGCCGGGCAGCATGGCTGCTCAAACCCGCCCTGCGAGACCCACGAGACGGGCACCACCAA T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153955029..153955185 26863196 MeRIP-seq:(Medium) rs782497232 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_257535,Human_RBP_ID_17328479,Human_RBP_ID_18197650,Human_RBP_ID_22122994,Human_RBP_ID_23099586,Human_RBP_ID_26835167,Human_RBP_ID_27145417,Human_RBP_ID_27380261 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_264267 96993 RMVar_ID_96993 Human_SNP_ID_735914270 m1A Human chrX - 153955078 153955078 153955078 AACATGGCCGGGCAGCATGGCTGCTCAAACCCACCCTGCGAGACCCACGAGACGGGCACCACCAA AACATGGCCGGGCAGCATGGCTGCTCAAACCCCCCCTGCGAGACCCACGAGACGGGCACCACCAA T G HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153955029..153955185 26863196 MeRIP-seq:(Medium) rs782497232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257535,Human_RBP_ID_17328479,Human_RBP_ID_18197650,Human_RBP_ID_22122994,Human_RBP_ID_23099586,Human_RBP_ID_26835167,Human_RBP_ID_27145417,Human_RBP_ID_27380261 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_264267 96994 RMVar_ID_96994 Human_SNP_ID_735916512 m1A Human chrX - 153964725 153964725 153964725 GTTCTGACTTCTGCCTCCTTCTGTTCCCCAGCAACCAACCAGTGGTTCATCCCAGCCGTGAGGGG GTTCTGACTTCTGCCTCCTTCTGTTCCCCAGCCACCAACCAGTGGTTCATCCCAGCCGTGAGGGG T G HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:153964691..153970912 32194978 MeRIP-seq:(Medium) rs1557117912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22693559 Human_Splice_Rec_2246740,Human_Splice_Rec_2246790 RMVar_hsa_circ_121535,RMVar_hsa_circ_90706,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_312030,RMVar_hsa_circ_9919,RMVar_hsa_circ_347831 96995 RMVar_ID_96995 Human_SNP_ID_735918068 m1A Human chrX - 153971510 153971510 153971510 TAAGGGGAGAGGCGCGAGACTTCACAAGCCGTACGGCGCGAGCCCCCAAACGGCCCTCGAGAGCT TAAGGGGAGAGGCGCGAGACTTCACAAGCCGTGCGGCGCGAGCCCCCAAACGGCCCTCGAGAGCT T C HCFC1 Ensembl:ENSG00000172534 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:153971460..153971668 26863196 MeRIP-seq:(Medium) rs1304240653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977757,Human_RBP_ID_5080164,Human_RBP_ID_9340344,Human_RBP_ID_22468593,Human_RBP_ID_26364305 96996 RMVar_ID_96996 Human_SNP_ID_735926979 m1A Human chrX + 154011611 154011611 154011611 TCACGGGTCTGTGCAGCCAGCAGCCTCCCAACATGCGCCAGCCTCCTCACTGGATGATGCCAGCC TCACGGGTCTGTGCAGCCAGCAGCCTCCCAACCTGCGCCAGCCTCCTCACTGGATGATGCCAGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154011476..154011872 26863196 MeRIP-seq:(Medium) rs1557127454 Functional Loss SNV dbSNP153 33..33 33 - - - 96997 RMVar_ID_96997 Human_SNP_ID_735927021 m1A Human chrX - 154011748 154011748 154011748 CAGCACTCTGCCGGCAGTGGGGGTGGGGGCCCATGCCCGCGGGGGAGAGAAGGAGGTGGCCCTGC CAGCACTCTGCCGGCAGTGGGGGTGGGGGCCCGTGCCCGCGGGGGAGAGAAGGAGGTGGCCCTGC T C IRAK1 Ensembl:ENSG00000184216 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154011701..154011775 32194978 MeRIP-seq:(Medium) rs781786701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731426,Human_RBP_ID_848719,Human_RBP_ID_5080210,Human_RBP_ID_5155247,Human_RBP_ID_8276915,Human_RBP_ID_27380363 Human_miRNA_ID_1062712,Human_miRNA_ID_2296622,Human_miRNA_ID_2494227,Human_miRNA_ID_3119426 RMVar_hsa_circ_89402,RMVar_hsa_circ_113730,RMVar_hsa_circ_121060,RMVar_hsa_circ_116102,RMVar_hsa_circ_111902,RMVar_hsa_circ_264271,RMVar_hsa_circ_264273,RMVar_hsa_circ_264275,RMVar_hsa_circ_79507,RMVar_hsa_circ_264274,RMVar_hsa_circ_264272,RMVar_hsa_circ_264270 96998 RMVar_ID_96998 Human_SNP_ID_735928093 m1A Human chrX - 154016401 154016399 154016402 AGCCACTGACCCCTCTGCTGGCTCAGAGGAGGAGAAGCCACAGGCAGGCAGAGGTGGGGGCTGCA AGCCACTGACCCCTCTGCTGGCTCAGAGGAG___AAGCCACAGGCAGGCAGAGGTGGGGGCTGCA TCTC T IRAK1 Ensembl:ENSG00000184216 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154016399..154016575 26863196 MeRIP-seq:(Medium) rs1435966543 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_19149782 RMVar_hsa_circ_89402,RMVar_hsa_circ_121060,RMVar_hsa_circ_116102,RMVar_hsa_circ_111902,RMVar_hsa_circ_264271,RMVar_hsa_circ_264273,RMVar_hsa_circ_79507,RMVar_hsa_circ_264274,RMVar_hsa_circ_264272,RMVar_hsa_circ_264270,RMVar_hsa_circ_345521,RMVar_hsa_circ_127709,RMVar_hsa_circ_264278,RMVar_hsa_circ_264279 96999 RMVar_ID_96999 Human_SNP_ID_735928491 m1A Human chrX + 154018047 154018047 154018047 GAGACGGTCCTCCAGGGAGCCGTTGGGCAGGAAGCCGTACACCAGGCAGTAGAAGCCGTTCTGAG GAGACGGTCCTCCAGGGAGCCGTTGGGCAGGAGGCCGTACACCAGGCAGTAGAAGCCGTTCTGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154018001..154018050 32194978 MeRIP-seq:(Medium) rs935561779 Functional Loss SNV dbSNP153 33..33 33 - - - 97000 RMVar_ID_97000 Human_SNP_ID_735928719 m1A Human chrX + 154018981 154018981 154018981 TTCCCTGGGGGGCAGGGGACACCTACCTTGGTAGAAGAAGGGGCTGGAGATGGCGGTGGAGGCCA TTCCCTGGGGGGCAGGGGACACCTACCTTGGTCGAAGAAGGGGCTGGAGATGGCGGTGGAGGCCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154018976..154019025 26863196 MeRIP-seq:(Medium) rs1557130522 Functional Loss SNV dbSNP153 33..33 33 - - - 97001 RMVar_ID_97001 Human_SNP_ID_735929536 m1A Human chrX - 154022811 154022811 154022811 GAGGGGAGCCAGGAGGGGATGTGTGTGTGCAGAGCTGAAGAGCTGGGGAGAATGGGGCTGGGCCC GAGGGGAGCCAGGAGGGGATGTGTGTGTGCAGCGCTGAAGAGCTGGGGAGAATGGGGCTGGGCCC T G MECP2 Ensembl:ENSG00000169057 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154022520..154022871 32194978 MeRIP-seq:(Medium) rs782289994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731491,Human_RBP_ID_7987005,Human_RBP_ID_9244855,Human_RBP_ID_18156348,Human_RBP_ID_18403774,Human_RBP_ID_24334791 Human_miRNA_ID_882736 97002 RMVar_ID_97002 Human_SNP_ID_735930937 m1A Human chrX - 154029571 154029544 154029571 CGGGTGGCGCTAGAGGCCATGGAGGCAGTAGGACAAGGTGCAGGCAGGCTGGCCTGGGGTCAGGC CGGGTGGCGCTAGAGGCCATGGAGGCAGTAGG___________________________TCAGGC ACCCCAGGCCAGCCTGCCTGCACCTTGT A MECP2 Ensembl:ENSG00000169057 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154029522..154029635 26863196 MeRIP-seq:(Medium) rs267608375 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_7987116,Human_RBP_ID_16847969 97003 RMVar_ID_97003 Human_SNP_ID_735931271 m1A Human chrX + 154030157 154030157 154030157 CAAAGCTACTTCTGGCCCTGGTTAGGTCTTCAACCTGACTGTGCTTGTCGGTAAGAAAAACATCC CAAAGCTACTTCTGGCCCTGGTTAGGTCTTCAGCCTGACTGTGCTTGTCGGTAAGAAAAACATCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154030106..154030256 32194978 MeRIP-seq:(Medium) rs1008863218 Functional Loss SNV dbSNP153 33..33 33 - - - 97004 RMVar_ID_97004 Human_SNP_ID_735931396 m1A Human chrX + 154030406 154030406 154030406 ACTCTCTCGGTCACGGGCGTCCGGCTGTCCACAGGCTCCTCTCTGTTTGGCCTTGGCATGGAGGA ACTCTCTCGGTCACGGGCGTCCGGCTGTCCACGGGCTCCTCTCTGTTTGGCCTTGGCATGGAGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154030355..154030456 32194978 MeRIP-seq:(Medium) rs1557134910 Functional Loss SNV dbSNP153 33..33 33 - - - 97005 RMVar_ID_97005 Human_SNP_ID_735931403 m1A Human chrX - 154030417 154030416 154030418 ACATTGTTTCATCCTCCATGCCAAGGCCAAACAGAGAGGAGCCTGTGGACAGCCGGACGCCCGTG ACATTGTTTCATCCTCCATGCCAAGGCCAAA__GAGAGGAGCCTGTGGACAGCCGGACGCCCGTG CTG C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154030367..154031023 26863196 MeRIP-seq:(Medium) rs786204316 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3977764,Human_RBP_ID_5057079,Human_RBP_ID_7987130,Human_RBP_ID_9340085,Human_RBP_ID_22346111,Human_RBP_ID_27145706,Human_RBP_ID_27550610 97006 RMVar_ID_97006 Human_SNP_ID_735931410 m1A Human chrX - 154030427 154030427 154030427 GAGCGCAAAGACATTGTTTCATCCTCCATGCCAAGGCCAAACAGAGAGGAGCCTGTGGACAGCCG GAGCGCAAAGACATTGTTTCATCCTCCATGCCGAGGCCAAACAGAGAGGAGCCTGTGGACAGCCG T C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154030376..154030450 32194978 MeRIP-seq:(Medium) rs375532936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977764,Human_RBP_ID_7987132,Human_RBP_ID_9340085,Human_RBP_ID_22346111,Human_RBP_ID_27145706,Human_RBP_ID_27550610 Human_miRNA_ID_1062714 97007 RMVar_ID_97007 Human_SNP_ID_735931512 m1A Human chrX + 154030575 154030575 154030575 AGCCGTCGCTCTCCAGTGAGCCTCCTCTGGGCATCTTCTCCTCTTTGCAGACGCTGCTGCTCAAG AGCCGTCGCTCTCCAGTGAGCCTCCTCTGGGCGTCTTCTCCTCTTTGCAGACGCTGCTGCTCAAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154030529..154030780 26863196 MeRIP-seq:(Medium) rs1210814372 Functional Loss SNV dbSNP153 33..33 33 - - - 97008 RMVar_ID_97008 Human_SNP_ID_735931605 m1A Human chrX - 154030699 154030629 154030699 ACCACCACCATCACCACCACTCAGAGTCCCCAAAGGCCCCCGTGCCACTGCTCCCACCCCTGCCC ACCACCACCATCACCACCACTCAGAGTCCCCA_________________________________ GTGGGGTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTT G MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:154030603..154030802 26863196 MeRIP-seq:(Medium) rs1557135353 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_27380432 Clinvar_Rec_576 97009 RMVar_ID_97009 Human_SNP_ID_735931626 m1A Human chrX - 154030699 154030634 154030699 ACCACCACCATCACCACCACTCAGAGTCCCCAAAGGCCCCCGTGCCACTGCTCCCACCCCTGCCC ACCACCACCATCACCACCACTCAGAGTCCCCA_________________________________ GTCCTCGGAGCTCTCGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTT G MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:154030603..154030802 26863196 MeRIP-seq:(Medium) rs1557135423 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_27380432 97010 RMVar_ID_97010 Human_SNP_ID_735931677 m1A Human chrX - 154030699 154030648 154030700 ACCACCACCATCACCACCACTCAGAGTCCCCAAAGGCCCCCGTGCCACTGCTCCCACCCCTGCCC ACCACCACCATCACCACCACTCAGAGTCCCC__________________________________ CGGGCTCAGGTGGAGGTGGGGGCAGGGGTGGGAGCAGTGGCACGGGGGCCTTT C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:154030603..154030802 26863196 MeRIP-seq:(Medium) rs1557135571 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_27380432 97011 RMVar_ID_97011 Human_SNP_ID_735931795 m1A Human chrX - 154030699 154030699 154030699 ACCACCACCATCACCACCACTCAGAGTCCCCAAAGGCCCCCGTGCCACTGCTCCCACCCCTGCCC ACCACCACCATCACCACCACTCAGAGTCCCCAGAGGCCCCCGTGCCACTGCTCCCACCCCTGCCC T C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:154030603..154030802 26863196 MeRIP-seq:(Medium) rs368461080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27380432 97012 RMVar_ID_97012 Human_SNP_ID_735932205 m1A Human chrX + 154031177 154031175 154031177 GTTTGAAAAGGCATCTTGACAAGGAGCTTCCCAGGACTTTTCTCCAGGACCCTTTTCACCTGCAC GTTTGAAAAGGCATCTTGACAAGGAGCTTCC__GGACTTTTCTCCAGGACCCTTTTCACCTGCAC CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154031126..154031290 26863196 MeRIP-seq:(Medium) rs267608510 Functional Loss DEL dbSNP153 32..33 33 - - - Clinvar_Rec_577 97013 RMVar_ID_97013 Human_SNP_ID_735932347 m1A Human chrX - 154031344 154031344 154031344 ACCCTAATGATTTTGACTTCACGGTAACTGGGAGAGGGAGCCCCTCCCGGCGAGAGCAGAAACCA ACCCTAATGATTTTGACTTCACGGTAACTGGGGGAGGGAGCCCCTCCCGGCGAGAGCAGAAACCA T C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154031301..154031389 26863196 MeRIP-seq:(Medium) rs727505391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712530,Human_RBP_ID_8239948,Human_RBP_ID_8933890,Human_RBP_ID_9317672 Clinvar_Rec_578 97014 RMVar_ID_97014 Human_SNP_ID_735932822 m1A Human chrX + 154032301 154032297 154032301 TGTCCAGCCTTCAGGCAGGGTGGGGTCATCATACATGGGTCCCCGGTCACGGATGATGGAGCGCC TGTCCAGCCTTCAGGCAGGGTGGGGTCAT____CATGGGTCCCCGGTCACGGATGATGGAGCGCC TCATA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154032251..154032525 32194978 MeRIP-seq:(Medium) rs1557137776 Functional Loss DEL dbSNP153 30..33 33 - - - 97015 RMVar_ID_97015 Human_SNP_ID_735932926 m1A Human chrX - 154032537 154032526 154032537 TTAACACTTCAGGGAAGAAAAGTCAGAAGACCAGGACCTCCAGGGCCTCAAGGACAAACCCCTCA TTAACACTTCAGGGAAGAAAAGTCAGAAGACC___________GGCCTCAAGGACAAACCCCTCA CCTGGAGGTCCT C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154032328..154032564 26863196 MeRIP-seq:(Medium) rs797045694 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_967645,Human_RBP_ID_7987141,Human_RBP_ID_26363504,Human_RBP_ID_26835841 Human_Splice_Rec_2247032,Human_Splice_Rec_2247036,Human_Splice_Rec_2247042,Human_Splice_Rec_2247048,Human_Splice_Rec_2247054,Human_Splice_Rec_2247058,Human_Splice_Rec_2247070,Human_Splice_Rec_2247074,Human_Splice_Rec_2247083,Human_Splice_Rec_2247087,Human_Splice_Rec_2247090,Human_Splice_Rec_2247092,Human_Splice_Rec_2247096,Human_Splice_Rec_2247098,Human_Splice_Rec_2247104,Human_Splice_Rec_2247108,Human_Splice_Rec_2247110,Human_Splice_Rec_2247112,Human_Splice_Rec_2247116 Clinvar_Rec_579 RMVar_hsa_circ_41777 97016 RMVar_ID_97016 Human_SNP_ID_735940791 m1A Human chrX + 154076353 154076353 154076353 TCCAGCCCCTGTTGACCTCTCTGATGGCCCGGACCCTTTGCCACTCTCCCCTAACCCCTCGTTCA TCCAGCCCCTGTTGACCTCTCTGATGGCCCGGCCCCTTTGCCACTCTCCCCTAACCCCTCGTTCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154076349..154076433 26863196 MeRIP-seq:(Medium) rs1242949017 Functional Loss SNV dbSNP153 33..33 33 - - - 97017 RMVar_ID_97017 Human_SNP_ID_735973753 m1A Human chrX - 154348776 154348776 154348776 CGCTACCCAAGCAGCCCCGCCCTCTTCCCCTCAACCCCGGCCCAGGCCGCCCTGGCCGCCCGCCT CGCTACCCAAGCAGCCCCGCCCTCTTCCCCTCGACCCCGGCCCAGGCCGCCCTGGCCGCCCGCCT T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:154348676..154348837 26863196 MeRIP-seq:(Medium) rs1260038758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799890,Human_RBP_ID_1071042,Human_RBP_ID_5057166,Human_RBP_ID_5124822,Human_RBP_ID_5155248,Human_RBP_ID_8939340,Human_RBP_ID_9317675,Human_RBP_ID_9340086,Human_RBP_ID_17667366,Human_RBP_ID_18197436,Human_RBP_ID_18963756,Human_RBP_ID_22534599,Human_RBP_ID_24444436,Human_RBP_ID_24526238,Human_RBP_ID_24555747,Human_RBP_ID_27380468 Human_Splice_Rec_2247507 Human_miRNA_ID_876798,Human_miRNA_ID_1160119,Human_miRNA_ID_1562458 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_124055,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_115493,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264310,RMVar_hsa_circ_264311,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284 97018 RMVar_ID_97018 Human_SNP_ID_735974369 m1A Human chrX - 154351078 154351078 154351078 TGGGGCCTTTCCGTCCTCCCTTGCCCTGGCTCAAGCACCCCCATCTAACCATGTCTGCTGTGCTT TGGGGCCTTTCCGTCCTCCCTTGCCCTGGCTCGAGCACCCCCATCTAACCATGTCTGCTGTGCTT T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154351076..154351100 32194978 MeRIP-seq:(Medium) rs1557175674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94418,Human_RBP_ID_3976940,Human_RBP_ID_22419709,Human_RBP_ID_22557170,Human_RBP_ID_22631469,Human_RBP_ID_22692818,Human_RBP_ID_22748649,Human_RBP_ID_24335010,Human_RBP_ID_26797073 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_264325 97019 RMVar_ID_97019 Human_SNP_ID_735974462 m1A Human chrX - 154351528 154351528 154351528 GCCCACCTGGGGCTCCTGGGCCCGGACAGACCAGAGCCACCGCAGAGACCAGGCCTTGGCCCTGT GCCCACCTGGGGCTCCTGGGCCCGGACAGACCTGAGCCACCGCAGAGACCAGGCCTTGGCCCTGT T A FLNA Ensembl:ENSG00000196924 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154351526..154351575 32194978 MeRIP-seq:(Medium) rs1253750403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22368953,Human_RBP_ID_22631470 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_264325 97020 RMVar_ID_97020 Human_SNP_ID_735974699 m1A Human chrX - 154352397 154352397 154352397 TGACAGCCCAGGTGACCAGCCCATCGGGCAAGACCCATGAGGCCGAGATCGTGGAAGGGGAGAAC TGACAGCCCAGGTGACCAGCCCATCGGGCAAGGCCCATGAGGCCGAGATCGTGGAAGGGGAGAAC T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154352251..154352450 32194978 MeRIP-seq:(Medium) rs782088697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94424,Human_RBP_ID_968144,Human_RBP_ID_3918992,Human_RBP_ID_3977767,Human_RBP_ID_5057239,Human_RBP_ID_8938937,Human_RBP_ID_9265440,Human_RBP_ID_9317691,Human_RBP_ID_18197449,Human_RBP_ID_18472969,Human_RBP_ID_19027791,Human_RBP_ID_22468165,Human_RBP_ID_24538314 Human_Splice_Rec_2247402,Human_Splice_Rec_2247492,Human_Splice_Rec_2247582,Human_Splice_Rec_2247675,Human_Splice_Rec_2247766,Human_Splice_Rec_2247896,Human_Splice_Rec_2247924,Human_Splice_Rec_2247932 Human_miRNA_ID_2158305,Human_miRNA_ID_2611937 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_1608,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_97350,RMVar_hsa_circ_264326,RMVar_hsa_circ_35178,RMVar_hsa_circ_46907,RMVar_hsa_circ_264328,RMVar_hsa_circ_264329,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_108906,RMVar_hsa_circ_78188,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264331,RMVar_hsa_circ_264332,RMVar_hsa_circ_264333,RMVar_hsa_circ_125720,RMVar_hsa_circ_264792,RMVar_hsa_circ_114261,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264340,RMVar_hsa_circ_264341,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335 97021 RMVar_ID_97021 Human_SNP_ID_735974773 m1A Human chrX - 154352677 154352677 154352677 CTGGAGGGGCGTGGGCCGTGCTTTCTTCCTGCAGGCAGCCCCTTCTCTGTGAAGGTGACAGGCGA CTGGAGGGGCGTGGGCCGTGCTTTCTTCCTGCTGGCAGCCCCTTCTCTGTGAAGGTGACAGGCGA T A FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154352549..154352679 26863196 MeRIP-seq:(Medium) rs1203603896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257627,Human_RBP_ID_5057255 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_97350,RMVar_hsa_circ_264326,RMVar_hsa_circ_46907,RMVar_hsa_circ_264328,RMVar_hsa_circ_264329,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_78188,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264332,RMVar_hsa_circ_264333,RMVar_hsa_circ_125720,RMVar_hsa_circ_114261,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_115724,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264340,RMVar_hsa_circ_264341,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_94395,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264346,RMVar_hsa_circ_264347,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343 97022 RMVar_ID_97022 Human_SNP_ID_735974950 m1A Human chrX - 154353156 154353156 154353156 CAAGGAGACGGGGGAGCACCTGGTGCATGTGAAGAAAAATGGCCAGCACGTGGCCAGCAGCCCCA CAAGGAGACGGGGGAGCACCTGGTGCATGTGAGGAAAAATGGCCAGCACGTGGCCAGCAGCCCCA T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1557176154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1071046,Human_RBP_ID_3976949,Human_RBP_ID_17717913,Human_RBP_ID_18156516,Human_RBP_ID_23099683,Human_RBP_ID_24555749 Human_Splice_Rec_2247396,Human_Splice_Rec_2247486,Human_Splice_Rec_2247577,Human_Splice_Rec_2247669,Human_Splice_Rec_2247760,Human_Splice_Rec_2247890,Human_Splice_Rec_2247936,Human_Splice_Rec_2247940 Human_miRNA_ID_879728,Human_miRNA_ID_1349163,Human_miRNA_ID_1813145,Human_miRNA_ID_2394063 RMVar_hsa_circ_246,RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_97350,RMVar_hsa_circ_264326,RMVar_hsa_circ_264328,RMVar_hsa_circ_264329,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264333,RMVar_hsa_circ_114261,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_115724,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264340,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_104448,RMVar_hsa_circ_109978,RMVar_hsa_circ_125060,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264346,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_113860,RMVar_hsa_circ_108965,RMVar_hsa_circ_109911,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_264361,RMVar_hsa_circ_87965,RMVar_hsa_circ_92898,RMVar_hsa_circ_95730,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_264363,RMVar_hsa_circ_76130,RMVar_hsa_circ_264364,RMVar_hsa_circ_264362,RMVar_hsa_circ_264357,RMVar_hsa_circ_264359,RMVar_hsa_circ_264360,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_349053,RMVar_hsa_circ_117495,RMVar_hsa_circ_264366,RMVar_hsa_circ_264367 97023 RMVar_ID_97023 Human_SNP_ID_735975172 m1A Human chrX + 154353965 154353965 154353965 TGTTGACGGTGAAGGTGGCAGGCTTGTTCACTACTCCATGGGTGAGGCCAGGCCCATAGGCAGTG TGTTGACGGTGAAGGTGGCAGGCTTGTTCACTCCTCCATGGGTGAGGCCAGGCCCATAGGCAGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154353902..154354073 26863196 MeRIP-seq:(Medium) rs1557176349 Functional Loss SNV dbSNP153 33..33 33 - - - 97024 RMVar_ID_97024 Human_SNP_ID_735975370 m1A Human chrX - 154354698 154354698 154354698 TCTCTGCTTTGCCCTGCAGGCTCTGGCTGGGGACCAGCCCTCGGTGCAGCCCCCTCTACGGTCTC TCTCTGCTTTGCCCTGCAGGCTCTGGCTGGGGCCCAGCCCTCGGTGCAGCCCCCTCTACGGTCTC T G FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154354651..154354950 26863196 MeRIP-seq:(Medium) rs1489824545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799907,Human_RBP_ID_968151,Human_RBP_ID_3977773,Human_RBP_ID_8938964,Human_RBP_ID_9265477,Human_RBP_ID_9317716,Human_RBP_ID_18197464,Human_RBP_ID_22468174,Human_RBP_ID_22748650 Human_Splice_Rec_2247384,Human_Splice_Rec_2247385,Human_Splice_Rec_2247474,Human_Splice_Rec_2247475,Human_Splice_Rec_2247565,Human_Splice_Rec_2247566,Human_Splice_Rec_2247657,Human_Splice_Rec_2247658,Human_Splice_Rec_2247748,Human_Splice_Rec_2247749,Human_Splice_Rec_2247841,Human_Splice_Rec_2247842,Human_Splice_Rec_2247878,Human_Splice_Rec_2247879,Human_Splice_Rec_2247946,Human_Splice_Rec_2247947,Human_Splice_Rec_2247955 Human_miRNA_ID_1562461,Human_miRNA_ID_2258882 RMVar_hsa_circ_89125,RMVar_hsa_circ_109959,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264301,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_264326,RMVar_hsa_circ_264328,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264333,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_115724,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_109978,RMVar_hsa_circ_125060,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264346,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_109911,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_264361,RMVar_hsa_circ_87965,RMVar_hsa_circ_95730,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_76130,RMVar_hsa_circ_264357,RMVar_hsa_circ_264359,RMVar_hsa_circ_264360,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_117495,RMVar_hsa_circ_1570,RMVar_hsa_circ_101438,RMVar_hsa_circ_86909,RMVar_hsa_circ_264366,RMVar_hsa_circ_264367,RMVar_hsa_circ_89248,RMVar_hsa_circ_79058,RMVar_hsa_circ_264368,RMVar_hsa_circ_264369,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_127445,RMVar_hsa_circ_264372,RMVar_hsa_circ_264373,RMVar_hsa_circ_91397,RMVar_hsa_circ_123700,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_264379,RMVar_hsa_circ_76786,RMVar_hsa_circ_81957,RMVar_hsa_circ_76219,RMVar_hsa_circ_264380,RMVar_hsa_circ_264377,RMVar_hsa_circ_264378,RMVar_hsa_circ_264376,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_94336,RMVar_hsa_circ_264386,RMVar_hsa_circ_264387 97025 RMVar_ID_97025 Human_SNP_ID_735975468 m1A Human chrX - 154354958 154354958 154354958 GACGTGCACCGTGTGCACGCCTGATGGCTCAGAGGTGGATGTGGACGTGGTGGAGAATGAGGACG GACGTGCACCGTGTGCACGCCTGATGGCTCAGGGGTGGATGTGGACGTGGTGGAGAATGAGGACG T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154354794..154355097 26863196 MeRIP-seq:(Medium) rs1445311327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712552,Human_RBP_ID_5080353,Human_RBP_ID_8933997,Human_RBP_ID_9265482,Human_RBP_ID_9317720,Human_RBP_ID_18454173 Human_miRNA_ID_209376,Human_miRNA_ID_1544673,Human_miRNA_ID_1597249 RMVar_hsa_circ_89125,RMVar_hsa_circ_109959,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264301,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_264326,RMVar_hsa_circ_264328,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264333,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_115724,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_109978,RMVar_hsa_circ_125060,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264346,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_95730,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_76130,RMVar_hsa_circ_264357,RMVar_hsa_circ_264359,RMVar_hsa_circ_264360,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_117495,RMVar_hsa_circ_1570,RMVar_hsa_circ_101438,RMVar_hsa_circ_86909,RMVar_hsa_circ_264366,RMVar_hsa_circ_264367,RMVar_hsa_circ_89248,RMVar_hsa_circ_79058,RMVar_hsa_circ_264368,RMVar_hsa_circ_264369,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_127445,RMVar_hsa_circ_264372,RMVar_hsa_circ_264373,RMVar_hsa_circ_91397,RMVar_hsa_circ_123700,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_264379,RMVar_hsa_circ_76786,RMVar_hsa_circ_81957,RMVar_hsa_circ_76219,RMVar_hsa_circ_264380,RMVar_hsa_circ_264377,RMVar_hsa_circ_264378,RMVar_hsa_circ_264376,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_94336,RMVar_hsa_circ_264386,RMVar_hsa_circ_366579,RMVar_hsa_circ_264387,RMVar_hsa_circ_119139,RMVar_hsa_circ_264389,RMVar_hsa_circ_264390,RMVar_hsa_circ_264388 97026 RMVar_ID_97026 Human_SNP_ID_735975629 m1A Human chrX - 154355627 154355627 154355627 CTAACCCCGCTGCCTCCCGCTTCCCCGCTCCCACTCCTGTCTGCACCGGGCTGCTTTTCACCGCG CTAACCCCGCTGCCTCCCGCTTCCCCGCTCCCTCTCCTGTCTGCACCGGGCTGCTTTTCACCGCG T A FLNA Ensembl:ENSG00000196924 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154355626..154355825 32194978 MeRIP-seq:(Medium) rs1364448973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18963758,Human_RBP_ID_19148724,Human_RBP_ID_21997348,Human_RBP_ID_22485093,Human_RBP_ID_26797392 RMVar_hsa_circ_109959,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_264326,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264333,RMVar_hsa_circ_89680,RMVar_hsa_circ_80213,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_109978,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_95730,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_76130,RMVar_hsa_circ_264357,RMVar_hsa_circ_264359,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_117495,RMVar_hsa_circ_101438,RMVar_hsa_circ_264366,RMVar_hsa_circ_264367,RMVar_hsa_circ_89248,RMVar_hsa_circ_79058,RMVar_hsa_circ_264369,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_127445,RMVar_hsa_circ_264372,RMVar_hsa_circ_264373,RMVar_hsa_circ_91397,RMVar_hsa_circ_123700,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_264379,RMVar_hsa_circ_81957,RMVar_hsa_circ_76219,RMVar_hsa_circ_264377,RMVar_hsa_circ_264378,RMVar_hsa_circ_264376,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_94336,RMVar_hsa_circ_264386,RMVar_hsa_circ_366579,RMVar_hsa_circ_264387,RMVar_hsa_circ_119139,RMVar_hsa_circ_264389,RMVar_hsa_circ_264390,RMVar_hsa_circ_264388 97027 RMVar_ID_97027 Human_SNP_ID_735975997 m1A Human chrX + 154357228 154357228 154357228 AAGCTGCCCCTCTGGGCAGGAGGGGCATTGGGAGTGGCCCCAGCAAGCAGCTTACCTAGCCCGTG AAGCTGCCCCTCTGGGCAGGAGGGGCATTGGGTGTGGCCCCAGCAAGCAGCTTACCTAGCCCGTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154357226..154357300 32194978 MeRIP-seq:(Medium) rs1557176999 Functional Loss SNV dbSNP153 33..33 33 - - - 97028 RMVar_ID_97028 Human_SNP_ID_735976222 m1A Human chrX - 154358170 154358169 154358170 CACGGTGAGCTCCGGGCACAGGCAGGGGAGGCAGGGGGGCCTGGGCGGCTGGAGTGTGGGCTGCG CACGGTGAGCTCCGGGCACAGGCAGGGGAGGC_GGGGGGCCTGGGCGGCTGGAGTGTGGGCTGCG CT C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154358166..154358669 26863196 MeRIP-seq:(Medium) rs781801861 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_109959,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_264326,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264333,RMVar_hsa_circ_89680,RMVar_hsa_circ_80213,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_109978,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_76130,RMVar_hsa_circ_264357,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_117495,RMVar_hsa_circ_101438,RMVar_hsa_circ_264366,RMVar_hsa_circ_264367,RMVar_hsa_circ_89248,RMVar_hsa_circ_79058,RMVar_hsa_circ_264369,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_127445,RMVar_hsa_circ_264372,RMVar_hsa_circ_264373,RMVar_hsa_circ_91397,RMVar_hsa_circ_123700,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_264379,RMVar_hsa_circ_81957,RMVar_hsa_circ_76219,RMVar_hsa_circ_264377,RMVar_hsa_circ_264378,RMVar_hsa_circ_264376,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_121134,RMVar_hsa_circ_91974,RMVar_hsa_circ_120722,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_94336,RMVar_hsa_circ_264386,RMVar_hsa_circ_264387,RMVar_hsa_circ_119139,RMVar_hsa_circ_122785,RMVar_hsa_circ_124264,RMVar_hsa_circ_264389,RMVar_hsa_circ_264390,RMVar_hsa_circ_123777,RMVar_hsa_circ_121870,RMVar_hsa_circ_113667,RMVar_hsa_circ_117115,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_264398,RMVar_hsa_circ_76841,RMVar_hsa_circ_87346,RMVar_hsa_circ_264400,RMVar_hsa_circ_264401,RMVar_hsa_circ_264399,RMVar_hsa_circ_264396,RMVar_hsa_circ_264397,RMVar_hsa_circ_264395,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_79644,RMVar_hsa_circ_107052,RMVar_hsa_circ_264404,RMVar_hsa_circ_264405,RMVar_hsa_circ_264403 97029 RMVar_ID_97029 Human_SNP_ID_735976259 m1A Human chrX + 154358301 154358301 154358301 GCAGGCACGCCAGTGGTGTTGAGCCCGGGGCCACTGGCCTTCACCTTGCTGGCATCATGAGTAGG GCAGGCACGCCAGTGGTGTTGAGCCCGGGGCCCCTGGCCTTCACCTTGCTGGCATCATGAGTAGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:154358251..154358350 26863196 MeRIP-seq:(Medium) rs782307585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264408 97030 RMVar_ID_97030 Human_SNP_ID_735976862 m1A Human chrX + 154360428 154360428 154360428 GTCCCCGGGCTCGGTGGGCACGTAGGACACGGAACATGTGCCATCCCCATTGTCCAAGCACTCGA GTCCCCGGGCTCGGTGGGCACGTAGGACACGGCACATGTGCCATCCCCATTGTCCAAGCACTCGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154359901..154360450 32194978 MeRIP-seq:(Medium) rs368441729 Functional Loss SNV dbSNP153 33..33 33 - - - 97031 RMVar_ID_97031 Human_SNP_ID_735977545 m1A Human chrX + 154362547 154362547 154362547 TCGATGTCAGCTTCGGCGGGGCCTACCACTCCAGGGGCACACTTGATGCCGATGCTGACGTCCCC TCGATGTCAGCTTCGGCGGGGCCTACCACTCCCGGGGCACACTTGATGCCGATGCTGACGTCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chrX:154362420..154362746;chrX:154362419..154362719 26863196 MeRIP-seq:(Medium) rs1414981021 Functional Loss SNV dbSNP153 33..33 33 - - - 97032 RMVar_ID_97032 Human_SNP_ID_735977977 m1A Human chrX - 154364131 154364131 154364131 CAATGAAGGCTGCCCTGTGGAGGCGTTGGTCAAGGACAACGGCAATGGCACTTACAGCTGCTCCT CAATGAAGGCTGCCCTGTGGAGGCGTTGGTCAGGGACAACGGCAATGGCACTTACAGCTGCTCCT T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs782024317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731629,Human_RBP_ID_966559,Human_RBP_ID_1229983,Human_RBP_ID_2072107,Human_RBP_ID_3918999,Human_RBP_ID_5637499,Human_RBP_ID_8934091,Human_RBP_ID_17717930,Human_RBP_ID_26363509,Human_RBP_ID_27380540,Human_RBP_ID_27834897 Human_Splice_Rec_2247350,Human_Splice_Rec_2247442,Human_Splice_Rec_2247533,Human_Splice_Rec_2247623,Human_Splice_Rec_2247717,Human_Splice_Rec_2247808 Human_miRNA_ID_656350,Human_miRNA_ID_2255877 RMVar_hsa_circ_120342,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_104303,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_264289,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264288,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_88211,RMVar_hsa_circ_87183,RMVar_hsa_circ_264355,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_101438,RMVar_hsa_circ_264366,RMVar_hsa_circ_79058,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_264372,RMVar_hsa_circ_264373,RMVar_hsa_circ_91397,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_76219,RMVar_hsa_circ_264376,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264390,RMVar_hsa_circ_123777,RMVar_hsa_circ_113667,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_76841,RMVar_hsa_circ_264395,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_264409,RMVar_hsa_circ_76357,RMVar_hsa_circ_91786,RMVar_hsa_circ_264410,RMVar_hsa_circ_96581,RMVar_hsa_circ_127623,RMVar_hsa_circ_369673,RMVar_hsa_circ_120029,RMVar_hsa_circ_264415,RMVar_hsa_circ_264416,RMVar_hsa_circ_264417,RMVar_hsa_circ_111917,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_100372,RMVar_hsa_circ_92546,RMVar_hsa_circ_84283,RMVar_hsa_circ_264420,RMVar_hsa_circ_264424,RMVar_hsa_circ_264425,RMVar_hsa_circ_264422,RMVar_hsa_circ_264423,RMVar_hsa_circ_264421,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_85464,RMVar_hsa_circ_105311,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_264436,RMVar_hsa_circ_122944,RMVar_hsa_circ_98810,RMVar_hsa_circ_124754,RMVar_hsa_circ_264438,RMVar_hsa_circ_264439,RMVar_hsa_circ_264440,RMVar_hsa_circ_264441,RMVar_hsa_circ_81763,RMVar_hsa_circ_81782,RMVar_hsa_circ_76577,RMVar_hsa_circ_85088,RMVar_hsa_circ_103284,RMVar_hsa_circ_264444,RMVar_hsa_circ_118986,RMVar_hsa_circ_86332,RMVar_hsa_circ_264447,RMVar_hsa_circ_264449,RMVar_hsa_circ_264448,RMVar_hsa_circ_264446,RMVar_hsa_circ_119322,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_90561,RMVar_hsa_circ_92234,RMVar_hsa_circ_90225,RMVar_hsa_circ_264452,RMVar_hsa_circ_264454,RMVar_hsa_circ_264456,RMVar_hsa_circ_264455,RMVar_hsa_circ_264453,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_67447,RMVar_hsa_circ_106423,RMVar_hsa_circ_264461,RMVar_hsa_circ_264462,RMVar_hsa_circ_264464,RMVar_hsa_circ_121384,RMVar_hsa_circ_90435,RMVar_hsa_circ_104766,RMVar_hsa_circ_264465,RMVar_hsa_circ_264466,RMVar_hsa_circ_264467,RMVar_hsa_circ_103668,RMVar_hsa_circ_264468 97033 RMVar_ID_97033 Human_SNP_ID_735977979 m1A Human chrX + 154364138 154364138 154364138 GCTGTAAGTGCCATTGCCGTTGTCCTTGACCAACGCCTCCACAGGGCAGCCTTCATTGTCCTGTC GCTGTAAGTGCCATTGCCGTTGTCCTTGACCAGCGCCTCCACAGGGCAGCCTTCATTGTCCTGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154364090..154364172 26863196 MeRIP-seq:(Medium) rs1557178637 Functional Loss SNV dbSNP153 33..33 33 - - - 97034 RMVar_ID_97034 Human_SNP_ID_735978146 m1A Human chrX - 154364721 154364721 154364721 CCAGGGCACTGAGGGGACTGGTGGCTGTTGTCAGGCTTCTCGGTGGAAGGGCCATCGCAGGCTAA CCAGGGCACTGAGGGGACTGGTGGCTGTTGTCGGGCTTCTCGGTGGAAGGGCCATCGCAGGCTAA T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chrX:154364676..154364725;chrX:154364526..154364725 26863196,32194978 MeRIP-seq:(Medium) rs786205183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94457,Human_RBP_ID_22631483 Clinvar_Rec_580 RMVar_hsa_circ_120342,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_104303,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_264289,RMVar_hsa_circ_86329,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_88211,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_264366,RMVar_hsa_circ_79058,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_264373,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_76219,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264390,RMVar_hsa_circ_123777,RMVar_hsa_circ_113667,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_76841,RMVar_hsa_circ_264395,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_264409,RMVar_hsa_circ_91786,RMVar_hsa_circ_127623,RMVar_hsa_circ_369673,RMVar_hsa_circ_120029,RMVar_hsa_circ_264416,RMVar_hsa_circ_264417,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_92546,RMVar_hsa_circ_84283,RMVar_hsa_circ_264420,RMVar_hsa_circ_264422,RMVar_hsa_circ_264423,RMVar_hsa_circ_264421,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_85464,RMVar_hsa_circ_105311,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_264436,RMVar_hsa_circ_98810,RMVar_hsa_circ_124754,RMVar_hsa_circ_264439,RMVar_hsa_circ_264440,RMVar_hsa_circ_264441,RMVar_hsa_circ_81763,RMVar_hsa_circ_81782,RMVar_hsa_circ_76577,RMVar_hsa_circ_85088,RMVar_hsa_circ_103284,RMVar_hsa_circ_264444,RMVar_hsa_circ_118986,RMVar_hsa_circ_86332,RMVar_hsa_circ_264447,RMVar_hsa_circ_264449,RMVar_hsa_circ_264448,RMVar_hsa_circ_264446,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_90561,RMVar_hsa_circ_92234,RMVar_hsa_circ_90225,RMVar_hsa_circ_264452,RMVar_hsa_circ_264454,RMVar_hsa_circ_264455,RMVar_hsa_circ_264453,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_106423,RMVar_hsa_circ_264461,RMVar_hsa_circ_264462,RMVar_hsa_circ_264464,RMVar_hsa_circ_121384,RMVar_hsa_circ_90435,RMVar_hsa_circ_264466,RMVar_hsa_circ_264467,RMVar_hsa_circ_103668,RMVar_hsa_circ_125068,RMVar_hsa_circ_264468,RMVar_hsa_circ_264469 97035 RMVar_ID_97035 Human_SNP_ID_735978168 m1A Human chrX - 154364804 154364804 154364804 GACGTGGGCACGCTGGGTAAGTTGGAGGCTGCAGCATGGGCACCTGGGGACAGACGATGGCAAGG GACGTGGGCACGCTGGGTAAGTTGGAGGCTGCGGCATGGGCACCTGGGGACAGACGATGGCAAGG T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154364801..154364825 26863196 MeRIP-seq:(Medium) rs1557178789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5412571 RMVar_hsa_circ_120342,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_104303,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_264289,RMVar_hsa_circ_86329,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_88211,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_264366,RMVar_hsa_circ_79058,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_264373,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_76219,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264390,RMVar_hsa_circ_123777,RMVar_hsa_circ_113667,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_76841,RMVar_hsa_circ_264395,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_264409,RMVar_hsa_circ_91786,RMVar_hsa_circ_127623,RMVar_hsa_circ_369673,RMVar_hsa_circ_120029,RMVar_hsa_circ_264416,RMVar_hsa_circ_264417,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_92546,RMVar_hsa_circ_84283,RMVar_hsa_circ_264420,RMVar_hsa_circ_264422,RMVar_hsa_circ_264423,RMVar_hsa_circ_264421,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_85464,RMVar_hsa_circ_105311,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_264436,RMVar_hsa_circ_98810,RMVar_hsa_circ_124754,RMVar_hsa_circ_264439,RMVar_hsa_circ_264440,RMVar_hsa_circ_264441,RMVar_hsa_circ_81763,RMVar_hsa_circ_81782,RMVar_hsa_circ_76577,RMVar_hsa_circ_85088,RMVar_hsa_circ_103284,RMVar_hsa_circ_264444,RMVar_hsa_circ_118986,RMVar_hsa_circ_86332,RMVar_hsa_circ_264447,RMVar_hsa_circ_264449,RMVar_hsa_circ_264448,RMVar_hsa_circ_264446,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_90561,RMVar_hsa_circ_92234,RMVar_hsa_circ_90225,RMVar_hsa_circ_264452,RMVar_hsa_circ_264454,RMVar_hsa_circ_264455,RMVar_hsa_circ_264453,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_106423,RMVar_hsa_circ_264461,RMVar_hsa_circ_264462,RMVar_hsa_circ_264464,RMVar_hsa_circ_121384,RMVar_hsa_circ_90435,RMVar_hsa_circ_264466,RMVar_hsa_circ_264467,RMVar_hsa_circ_103668,RMVar_hsa_circ_125068,RMVar_hsa_circ_264468,RMVar_hsa_circ_264469 97036 RMVar_ID_97036 Human_SNP_ID_735978312 m1A Human chrX - 154365214 154365214 154365214 CGTGAAGCAGAAGGACCTGGGGGATGGCGTGTATGGCTTCGAGTATTACCCCATGGTCCCTGGAA CGTGAAGCAGAAGGACCTGGGGGATGGCGTGTGTGGCTTCGAGTATTACCCCATGGTCCCTGGAA T C FLNA Ensembl:ENSG00000196924 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154364588..154365498 26863196 MeRIP-seq:(Medium) rs1557178932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94459,Human_RBP_ID_3976976,Human_RBP_ID_5080416,Human_RBP_ID_5637506,Human_RBP_ID_8934106,Human_RBP_ID_9340363,Human_RBP_ID_18156032,Human_RBP_ID_18197712 Human_Splice_Rec_2247342,Human_Splice_Rec_2247343,Human_Splice_Rec_2247434,Human_Splice_Rec_2247435,Human_Splice_Rec_2247525,Human_Splice_Rec_2247526,Human_Splice_Rec_2247615,Human_Splice_Rec_2247616,Human_Splice_Rec_2247709,Human_Splice_Rec_2247710,Human_Splice_Rec_2247800,Human_Splice_Rec_2247801,Human_Splice_Rec_2247963 Clinvar_Rec_581 RMVar_hsa_circ_120342,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_104303,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_86329,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_264366,RMVar_hsa_circ_79058,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_264373,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_76219,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264390,RMVar_hsa_circ_113667,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_76841,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_264409,RMVar_hsa_circ_91786,RMVar_hsa_circ_127623,RMVar_hsa_circ_369673,RMVar_hsa_circ_120029,RMVar_hsa_circ_264416,RMVar_hsa_circ_264417,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_92546,RMVar_hsa_circ_84283,RMVar_hsa_circ_264420,RMVar_hsa_circ_264422,RMVar_hsa_circ_264423,RMVar_hsa_circ_264421,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_85464,RMVar_hsa_circ_105311,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_264436,RMVar_hsa_circ_98810,RMVar_hsa_circ_264439,RMVar_hsa_circ_264440,RMVar_hsa_circ_81763,RMVar_hsa_circ_81782,RMVar_hsa_circ_76577,RMVar_hsa_circ_85088,RMVar_hsa_circ_103284,RMVar_hsa_circ_264444,RMVar_hsa_circ_86332,RMVar_hsa_circ_264447,RMVar_hsa_circ_264449,RMVar_hsa_circ_264448,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_90561,RMVar_hsa_circ_92234,RMVar_hsa_circ_90225,RMVar_hsa_circ_264452,RMVar_hsa_circ_264454,RMVar_hsa_circ_264455,RMVar_hsa_circ_264453,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_106423,RMVar_hsa_circ_264461,RMVar_hsa_circ_264462,RMVar_hsa_circ_264464,RMVar_hsa_circ_121384,RMVar_hsa_circ_90435,RMVar_hsa_circ_264466,RMVar_hsa_circ_264467,RMVar_hsa_circ_103668,RMVar_hsa_circ_78301,RMVar_hsa_circ_264468,RMVar_hsa_circ_82883,RMVar_hsa_circ_264471,RMVar_hsa_circ_45338,RMVar_hsa_circ_264470,RMVar_hsa_circ_269751,RMVar_hsa_circ_264474,RMVar_hsa_circ_122240,RMVar_hsa_circ_264475 97037 RMVar_ID_97037 Human_SNP_ID_735978834 m1A Human chrX - 154366852 154366852 154366852 GCTGGCCCGTGGTTGGCTCGCCTTCCCCTGCCAGGCATCGAGCCCACAGGCAACATGGTGAAGAA GCTGGCCCGTGGTTGGCTCGCCTTCCCCTGCCGGGCATCGAGCCCACAGGCAACATGGTGAAGAA T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:154366851..154366875 26863196 MeRIP-seq:(Medium) rs1557179425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19148741 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_86329,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_104073,RMVar_hsa_circ_264373,RMVar_hsa_circ_85690,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_113166,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_127623,RMVar_hsa_circ_264417,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_264420,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_81763,RMVar_hsa_circ_85088,RMVar_hsa_circ_264444,RMVar_hsa_circ_264449,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_264462,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_78301,RMVar_hsa_circ_264470,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_108820,RMVar_hsa_circ_99004,RMVar_hsa_circ_264479,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_264480,RMVar_hsa_circ_47631,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_95132,RMVar_hsa_circ_264484,RMVar_hsa_circ_264485 97038 RMVar_ID_97038 Human_SNP_ID_735978991 m1A Human chrX + 154367497 154367497 154367497 GCCTTGGGGAACTGGGACAGGTAGGTCATGACAGAGTGCTCGTCCACGTTGGGGTCCACAATCTC GCCTTGGGGAACTGGGACAGGTAGGTCATGACGGAGTGCTCGTCCACGTTGGGGTCCACAATCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154367446..154367560 26863196 MeRIP-seq:(Medium) rs782357419 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_582,Clinvar_Rec_5471 97039 RMVar_ID_97039 Human_SNP_ID_735979064 m1A Human chrX - 154367740 154367740 154367740 GGCCCCCAGACTCACAGCCTCCCTTGCGCCACAGGCCTGTGTCCTGACTGGGACTCTTGGGACGC GGCCCCCAGACTCACAGCCTCCCTTGCGCCACGGGCCTGTGTCCTGACTGGGACTCTTGGGACGC T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chrX:154367715..154368019;chrX:154367626..154367750 26863196,32194978 MeRIP-seq:(Medium) rs111481417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94469,Human_RBP_ID_5057544 Human_Splice_Rec_2247329,Human_Splice_Rec_2247421,Human_Splice_Rec_2247512,Human_Splice_Rec_2247602,Human_Splice_Rec_2247696,Human_Splice_Rec_2247787 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_85690,RMVar_hsa_circ_264374,RMVar_hsa_circ_113166,RMVar_hsa_circ_264387,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_81763,RMVar_hsa_circ_85088,RMVar_hsa_circ_264444,RMVar_hsa_circ_264449,RMVar_hsa_circ_126822,RMVar_hsa_circ_264450,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_99004,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_264480,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_95132,RMVar_hsa_circ_264484,RMVar_hsa_circ_264485 97040 RMVar_ID_97040 Human_SNP_ID_735979129 m1A Human chrX - 154367955 154367955 154367955 GGATGAGGAGGCCAAGAAGCAGACCCCCAAGCAGAGGCTCCTGGGCTGGATCCAGAACAAGCTGC GGATGAGGAGGCCAAGAAGCAGACCCCCAAGCCGAGGCTCCTGGGCTGGATCCAGAACAAGCTGC T G FLNA Ensembl:ENSG00000196924 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154367359..154368121 26863196 MeRIP-seq:(Medium) rs863223628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_318341,Human_RBP_ID_968198,Human_RBP_ID_5080438,Human_RBP_ID_5637514,Human_RBP_ID_23099712 Human_miRNA_ID_2209709,Human_miRNA_ID_2899531,Human_miRNA_ID_2975420,Human_miRNA_ID_2995765,Human_miRNA_ID_3008615,Human_miRNA_ID_3034314 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_85690,RMVar_hsa_circ_264374,RMVar_hsa_circ_113166,RMVar_hsa_circ_264387,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_81763,RMVar_hsa_circ_85088,RMVar_hsa_circ_264444,RMVar_hsa_circ_264449,RMVar_hsa_circ_126822,RMVar_hsa_circ_264450,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_99004,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_264480,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_95132,RMVar_hsa_circ_264484,RMVar_hsa_circ_264485,RMVar_hsa_circ_269634 97041 RMVar_ID_97041 Human_SNP_ID_735979872 m1A Human chrX - 154371164 154371164 154371164 CGGGCGGCGGCGTCGACACGCGGGACGCCGAGATGCCGGCCACCGAGAAGGACCTGGCGGAGGAC CGGGCGGCGGCGTCGACACGCGGGACGCCGAGGTGCCGGCCACCGAGAAGGACCTGGCGGAGGAC T C FLNA Ensembl:ENSG00000196924 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154370928..154371350 26863196 MeRIP-seq:(Medium) rs1557180226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94473,Human_RBP_ID_848603,Human_RBP_ID_3919006,Human_RBP_ID_5076396 Human_miRNA_ID_2018179 Clinvar_Rec_583 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_127304,RMVar_hsa_circ_264321,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_96481,RMVar_hsa_circ_264418,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_83014,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_264484,RMVar_hsa_circ_264489 97042 RMVar_ID_97042 Human_SNP_ID_735979915 m1A Human chrX - 154371217 154371217 154371217 CAAAATGAGTAGCTCCCACTCTCGGGCGGGCCAGAGCGCAGCAGGCGCGGCTCCGGGCGGCGGCG CAAAATGAGTAGCTCCCACTCTCGGGCGGGCCGGAGCGCAGCAGGCGCGGCTCCGGGCGGCGGCG T C FLNA Ensembl:ENSG00000196924 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chrX:154371201..154371225;chrX:154371176..154371275 26863196,32194978 MeRIP-seq:(Medium) rs781988041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94473,Human_RBP_ID_5076859 Human_miRNA_ID_2513634,Human_miRNA_ID_3056454 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_127304,RMVar_hsa_circ_264321,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_96481,RMVar_hsa_circ_264418,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_83014,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_264484,RMVar_hsa_circ_264489 97043 RMVar_ID_97043 Human_SNP_ID_735979916 m1A Human chrX - 154371217 154371217 154371217 CAAAATGAGTAGCTCCCACTCTCGGGCGGGCCAGAGCGCAGCAGGCGCGGCTCCGGGCGGCGGCG CAAAATGAGTAGCTCCCACTCTCGGGCGGGCCCGAGCGCAGCAGGCGCGGCTCCGGGCGGCGGCG T G FLNA Ensembl:ENSG00000196924 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chrX:154371201..154371225;chrX:154371176..154371275 26863196,32194978 MeRIP-seq:(Medium) rs781988041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94473,Human_RBP_ID_5076859 Human_miRNA_ID_2513634,Human_miRNA_ID_3056454 RMVar_hsa_circ_105445,RMVar_hsa_circ_97011,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_127304,RMVar_hsa_circ_264321,RMVar_hsa_circ_124437,RMVar_hsa_circ_88211,RMVar_hsa_circ_264349,RMVar_hsa_circ_264348,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_96481,RMVar_hsa_circ_264418,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_90435,RMVar_hsa_circ_264467,RMVar_hsa_circ_83014,RMVar_hsa_circ_83946,RMVar_hsa_circ_104740,RMVar_hsa_circ_121439,RMVar_hsa_circ_264481,RMVar_hsa_circ_264482,RMVar_hsa_circ_97120,RMVar_hsa_circ_264483,RMVar_hsa_circ_264484,RMVar_hsa_circ_264489 97044 RMVar_ID_97044 Human_SNP_ID_735981048 m1A Human chrX - 154376878 154376878 154376878 GGAATTCTAGATTTGCCTTCTCCCTAAGGAGCACCCCCCACCCGTTCTGTACCTGCCTCGACACT GGAATTCTAGATTTGCCTTCTCCCTAAGGAGCCCCCCCCACCCGTTCTGTACCTGCCTCGACACT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154376829..154377042 26863196 MeRIP-seq:(Medium) rs1557181655 Functional Loss SNV dbSNP153 33..33 33 - - - 97045 RMVar_ID_97045 Human_SNP_ID_735981909 m1A Human chrX - 154380283 154380283 154380283 GCCCTGGACGGGCCGGCAGACTCGGGCTCCCCATAAGTCCTGGTGGTGAAGTAGCTCTCTTCATA GCCCTGGACGGGCCGGCAGACTCGGGCTCCCCGTAAGTCCTGGTGGTGAAGTAGCTCTCTTCATA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154380202..154380324 26863196 MeRIP-seq:(Medium) rs1342409944 Functional Loss SNV dbSNP153 33..33 33 - - - 97046 RMVar_ID_97046 Human_SNP_ID_735982042 m1A Human chrX - 154380776 154380773 154380776 ACGCACCTATCCTTGCACTCCTCTTCAGAAGAAGACAAAAGATCGTCATCATGCACCTGCAGAAG ACGCACCTATCCTTGCACTCCTCTTCAGAAGA___CAAAAGATCGTCATCATGCACCTGCAGAAG GTCT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154380751..154380775 32194978 MeRIP-seq:(Medium) rs1557182551 Functional Loss DEL dbSNP153 33..35 33 - - - 97047 RMVar_ID_97047 Human_SNP_ID_735982044 m1A Human chrX - 154380776 154380776 154380776 ACGCACCTATCCTTGCACTCCTCTTCAGAAGAAGACAAAAGATCGTCATCATGCACCTGCAGAAG ACGCACCTATCCTTGCACTCCTCTTCAGAAGACGACAAAAGATCGTCATCATGCACCTGCAGAAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154380751..154380775 32194978 MeRIP-seq:(Medium) rs1209782193 Functional Loss SNV dbSNP153 33..33 33 - - - 97048 RMVar_ID_97048 Human_SNP_ID_735982144 m1A Human chrX - 154381012 154381012 154381012 ACGGCGGGTGAGCCATGAAGAGGAAGATGATGAGGAGGACATAAAAGAGGTGGAGGAGGAAGTAG ACGGCGGGTGAGCCATGAAGAGGAAGATGATGTGGAGGACATAAAAGAGGTGGAGGAGGAAGTAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154380883..154381414 26863196 MeRIP-seq:(Medium) rs1557182650 Functional Loss SNV dbSNP153 33..33 33 - - - 97049 RMVar_ID_97049 Human_SNP_ID_735982154 m1A Human chrX - 154381030 154381030 154381030 GTTTTCAGGCCGGATGGCACGGCGGGTGAGCCATGAAGAGGAAGATGATGAGGAGGACATAAAAG GTTTTCAGGCCGGATGGCACGGCGGGTGAGCCGTGAAGAGGAAGATGATGAGGAGGACATAAAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:154380980..154381080 32194978 MeRIP-seq:(Medium) rs374981936 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_584 97050 RMVar_ID_97050 Human_SNP_ID_735984702 m1A Human chrX - 154398396 154398396 154398396 GGCACCGCAAGAGACGACAACTGCGCTTACTCACCACACCGAAGGGAAAGAGGCGCTCCTCCGCC GGCACCGCAAGAGACGACAACTGCGCTTACTCGCCACACCGAAGGGAAAGAGGCGCTCCTCCGCC T C AC245140.2 Ensembl:ENSG00000280195 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:154398351..154398550 26863196 MeRIP-seq:(Medium) rs1557184854 Functional Loss SNV dbSNP153 33..33 33 - - - 97051 RMVar_ID_97051 Human_SNP_ID_735984720 m1A Human chrX + 154398407 154398407 154398407 GCCTCTTTCCCTTCGGTGTGGTGAGTAAGCGCAGTTGTCGTCTCTTGCGGTGCCGTTGCTGGTTC GCCTCTTTCCCTTCGGTGTGGTGAGTAAGCGCGGTTGTCGTCTCTTGCGGTGCCGTTGCTGGTTC A G RPL10 Ensembl:ENSG00000147403 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154398376..154398650 26863196 MeRIP-seq:(Medium) rs782459394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731688,Human_RBP_ID_1229986,Human_RBP_ID_1712579,Human_RBP_ID_5057688,Human_RBP_ID_5272142,Human_RBP_ID_8715482,Human_RBP_ID_18427897,Human_RBP_ID_18917356,Human_RBP_ID_19149839,Human_RBP_ID_21811259,Human_RBP_ID_22841053,Human_RBP_ID_24335064 RMVar_hsa_circ_115895,RMVar_hsa_circ_264494 97052 RMVar_ID_97052 Human_SNP_ID_735984721 m1A Human chrX + 154398407 154398407 154398407 GCCTCTTTCCCTTCGGTGTGGTGAGTAAGCGCAGTTGTCGTCTCTTGCGGTGCCGTTGCTGGTTC GCCTCTTTCCCTTCGGTGTGGTGAGTAAGCGCTGTTGTCGTCTCTTGCGGTGCCGTTGCTGGTTC A T RPL10 Ensembl:ENSG00000147403 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154398376..154398650 26863196 MeRIP-seq:(Medium) rs782459394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731688,Human_RBP_ID_1229986,Human_RBP_ID_1712579,Human_RBP_ID_5057688,Human_RBP_ID_5272142,Human_RBP_ID_8715482,Human_RBP_ID_18427897,Human_RBP_ID_18917356,Human_RBP_ID_19149839,Human_RBP_ID_21811259,Human_RBP_ID_22841053,Human_RBP_ID_24335064 RMVar_hsa_circ_115895,RMVar_hsa_circ_264494 97053 RMVar_ID_97053 Human_SNP_ID_735984771 m1A Human chrX - 154398484 154398484 154398484 GACACCAGGATCTTCAGTGGCTGCAACGAAAAAGAGAGAGTCGGAACGGAAGACGAGAACAGACC GACACCAGGATCTTCAGTGGCTGCAACGAAAATGAGAGAGTCGGAACGGAAGACGAGAACAGACC T A AC245140.2 Ensembl:ENSG00000280195 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chrX:154398407..154398561;chrX:154398354..154398504 26863196,32194978 MeRIP-seq:(Medium) rs782442208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5639641 97054 RMVar_ID_97054 Human_SNP_ID_735984866 m1A Human chrX - 154398777 154398777 154398777 GTATCTAGCGCCCGAAAATGCGGTGAGCTTGCAGGACACAGGCAGAGATACGAGGGAACCGTCGC GTATCTAGCGCCCGAAAATGCGGTGAGCTTGCCGGACACAGGCAGAGATACGAGGGAACCGTCGC T G AC245140.2 Ensembl:ENSG00000280195 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154398727..154398812 26863196 MeRIP-seq:(Medium) rs1166579068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5639643 97055 RMVar_ID_97055 Human_SNP_ID_735985016 m1A Human chrX - 154399295 154399295 154399295 GTGAAAAAACACAGGTTAGGTGAGGTTCACAGAAAGCCCAACAGGCACTTTGCCCCTCAAGGAAC GTGAAAAAACACAGGTTAGGTGAGGTTCACAGGAAGCCCAACAGGCACTTTGCCCCTCAAGGAAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:154399292..154399577 26863410 MeRIP-seq:(Medium) rs781947636 Functional Loss SNV dbSNP153 33..33 33 - - - 97056 RMVar_ID_97056 Human_SNP_ID_735985366 m1A Human chrX - 154400630 154400630 154400630 GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACATACCTTCTGGCGGCCAGGAAACTTGAACTTGG GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACTTACCTTCTGGCGGCCAGGAAACTTGAACTTGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154400604..154400687 26863196 MeRIP-seq:(Medium) rs782342444 Functional Loss SNV dbSNP153 33..33 33 - - - 97057 RMVar_ID_97057 Human_SNP_ID_735985367 m1A Human chrX - 154400630 154400630 154400630 GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACATACCTTCTGGCGGCCAGGAAACTTGAACTTGG GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACGTACCTTCTGGCGGCCAGGAAACTTGAACTTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154400604..154400687 26863196 MeRIP-seq:(Medium) rs782342444 Functional Loss SNV dbSNP153 33..33 33 - - - 97058 RMVar_ID_97058 Human_SNP_ID_735985368 m1A Human chrX - 154400630 154400630 154400630 GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACATACCTTCTGGCGGCCAGGAAACTTGAACTTGG GCAAAGGTGGGAGAAGGGGGCTGCAGCACTACCTACCTTCTGGCGGCCAGGAAACTTGAACTTGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154400604..154400687 26863196 MeRIP-seq:(Medium) rs782342444 Functional Loss SNV dbSNP153 33..33 33 - - - 97059 RMVar_ID_97059 Human_SNP_ID_735987919 m1A Human chrX - 154411726 154411722 154411726 CACTGGCCCCTGACTGGCCCGCGCACGGACGGACGGGGGCGCGGCGCAACAGGGGACTGGACCGA CACTGGCCCCTGACTGGCCCGCGCACGGACGG____GGGCGCGGCGCAACAGGGGACTGGACCGA CCCGT C DNASE1L1 Ensembl:ENSG00000013563 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154411567..154411795 26863196 MeRIP-seq:(Medium) rs1555939876 Functional Loss DEL dbSNP153 33..36 33 - - - 97060 RMVar_ID_97060 Human_SNP_ID_735987969 m1A Human chrX + 154411844 154411844 154411844 CGCTGGGAGCGCCGGCCGCGGGCCGGGTGGGGATGCCTCTGCACGTGAAGTGGCCGTTCCCCGCG CGCTGGGAGCGCCGGCCGCGGGCCGGGTGGGGTTGCCTCTGCACGTGAAGTGGCCGTTCCCCGCG A T TAZ Ensembl:ENSG00000102125 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:154411801..154412059 26863196 MeRIP-seq:(Medium) rs12845698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076404 97061 RMVar_ID_97061 Human_SNP_ID_735989318 m1A Human chrX - 154419038 154419038 154419038 CCTGGCTGCCAGCCGACCGCTCTCGGAGCCTCATGCGTTCCTTTCTCTTTGAAGGTGCCACTCCT CCTGGCTGCCAGCCGACCGCTCTCGGAGCCTCTTGCGTTCCTTTCTCTTTGAAGGTGCCACTCCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154418999..154419281 26863196 MeRIP-seq:(Medium) rs782569502 Functional Loss SNV dbSNP153 33..33 33 - - - 97062 RMVar_ID_97062 Human_SNP_ID_735989724 m1A Human chrX - 154420904 154420904 154420904 GAATGAAGTCCGTCAGGGCTTTCCGCATCTCCACCTGAGGGAAAGGACCAGGGATGGCCTGCACC GAATGAAGTCCGTCAGGGCTTTCCGCATCTCCCCCTGAGGGAAAGGACCAGGGATGGCCTGCACC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154420901..154420975 32194978 MeRIP-seq:(Medium) rs782746355 Functional Loss SNV dbSNP153 33..33 33 - - - 97063 RMVar_ID_97063 Human_SNP_ID_735991227 m1A Human chrX + 154428331 154428331 154428331 AACATAGCTAGACCCCGTCTCTAAAGAAAAAAAAAAGACAAAAGAAGAGAACAACAACAAAAAAA AACATAGCTAGACCCCGTCTCTAAAGAAAAAACAAAGACAAAAGAAGAGAACAACAACAAAAAAA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154428329..154428429 26863196 MeRIP-seq:(Medium) rs992537233 Functional Loss SNV dbSNP153 33..33 33 - - - 97064 RMVar_ID_97064 Human_SNP_ID_735991341 m1A Human chrX + 154428726 154428726 154428726 TGATGGCGGCCATGGCGACGGCTCGAGTGCGGATGGGGCCGCGGTGCGCCCAGGCGCTCTGGCGC TGATGGCGGCCATGGCGACGGCTCGAGTGCGGGTGGGGCCGCGGTGCGCCCAGGCGCTCTGGCGC A G ATP6AP1 Ensembl:ENSG00000071553 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:154428676..154428875 26863196 MeRIP-seq:(Medium) rs1557196231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257078,Human_RBP_ID_848123,Human_RBP_ID_5057855,Human_RBP_ID_5330618,Human_RBP_ID_18472985,Human_RBP_ID_22467836,Human_RBP_ID_23217088 RMVar_hsa_circ_99466,RMVar_hsa_circ_264507 97065 RMVar_ID_97065 Human_SNP_ID_735991406 m1A Human chrX + 154428817 154428817 154428817 GTTGGCGGCGGCGGCGGCGGCGGCAGCGGCGGAGCAGCAGGTCCCGCTGGTGCTGTGGTCGAGTG GTTGGCGGCGGCGGCGGCGGCGGCAGCGGCGGGGCAGCAGGTCCCGCTGGTGCTGTGGTCGAGTG A G ATP6AP1 Ensembl:ENSG00000071553 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154428676..154428850 26863196 MeRIP-seq:(Medium) rs920550880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257079,Human_RBP_ID_799121,Human_RBP_ID_848124,Human_RBP_ID_968377,Human_RBP_ID_5075977,Human_RBP_ID_5244865,Human_RBP_ID_9340373,Human_RBP_ID_18148005,Human_RBP_ID_18472986,Human_RBP_ID_22123015,Human_RBP_ID_22467837,Human_RBP_ID_22777823,Human_RBP_ID_23217088 Human_Splice_Rec_2248712,Human_Splice_Rec_2248721,Human_Splice_Rec_2248732,Human_Splice_Rec_2248749,Human_Splice_Rec_2248753,Human_Splice_Rec_2248757,Human_Splice_Rec_2248774 Human_miRNA_ID_2305318,Human_miRNA_ID_2513635,Human_miRNA_ID_3056455 RMVar_hsa_circ_99466,RMVar_hsa_circ_264507 97066 RMVar_ID_97066 Human_SNP_ID_735991811 m1A Human chrX - 154430868 154430868 154430868 CCCCTTTCTCTCACTCACTGTGCTCCAGCCACACCAGCTCTTCCTTGAGCTGGCCAAGAGCACAC CCCCTTTCTCTCACTCACTGTGCTCCAGCCACGCCAGCTCTTCCTTGAGCTGGCCAAGAGCACAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154430865..154430964 26863196 MeRIP-seq:(Medium) rs1320512582 Functional Loss SNV dbSNP153 33..33 33 - - - 97067 RMVar_ID_97067 Human_SNP_ID_735992874 m1A Human chrX - 154435804 154435804 154435804 ATGGTCTTGAGGCTGAGGATCATGTGCAGGCCATAGGTGAAGATGAAGAGCATGAACAGGGAGGT ATGGTCTTGAGGCTGAGGATCATGTGCAGGCCGTAGGTGAAGATGAAGAGCATGAACAGGGAGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154435757..154435825 26863196 MeRIP-seq:(Medium) rs1557197592 Functional Loss SNV dbSNP153 33..33 33 - - - 97068 RMVar_ID_97068 Human_SNP_ID_735992931 m1A Human chrX - 154436060 154436059 154436060 AATATGTACACCTTGTTGGGAGAGATGGGGGCAGCCCAAGAAAGCTCCTCAGCGGGCTGAAGAGG AATATGTACACCTTGTTGGGAGAGATGGGGGC_GCCCAAGAAAGCTCCTCAGCGGGCTGAAGAGG CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154436014..154436085 26863196 MeRIP-seq:(Medium) rs1392547764 Functional Loss DEL dbSNP153 33..33 33 - - - 97069 RMVar_ID_97069 Human_SNP_ID_735993307 m1A Human chrX + 154437276 154437276 154437276 GAGGCCTGACCATGGACGAGGAATACGATGTGATCGTGCTGGGGACCGGTCTCACCGTAAGTGCG GAGGCCTGACCATGGACGAGGAATACGATGTGGTCGTGCTGGGGACCGGTCTCACCGTAAGTGCG A G GDI1 Ensembl:ENSG00000203879 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:154437176..154437300 26863410 MeRIP-seq:(Medium) rs781939489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731800,Human_RBP_ID_968473,Human_RBP_ID_1712616,Human_RBP_ID_3976994,Human_RBP_ID_5057937,Human_RBP_ID_8944831,Human_RBP_ID_9340375,Human_RBP_ID_16849924,Human_RBP_ID_18148020,Human_RBP_ID_18174037,Human_RBP_ID_18427899,Human_RBP_ID_18454177,Human_RBP_ID_19027806,Human_RBP_ID_23217353,Human_RBP_ID_24335141,Human_RBP_ID_26363521 Human_Splice_Rec_2248823,Human_Splice_Rec_2248831,Human_Splice_Rec_2248837,Human_Splice_Rec_2248845,Human_Splice_Rec_2248865,Human_Splice_Rec_2248875,Human_Splice_Rec_2248882 Human_miRNA_ID_2258885 97070 RMVar_ID_97070 Human_SNP_ID_735993655 m1A Human chrX + 154438503 154438503 154438503 GGTAGGAGCGGAGGCAGGTGGGAGTGCAGCGGATGGTGTCACCCTCCCCCAGGAATGCATCCTGT GGTAGGAGCGGAGGCAGGTGGGAGTGCAGCGGCTGGTGTCACCCTCCCCCAGGAATGCATCCTGT A C GDI1 Ensembl:ENSG00000203879 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154438501..154438600 26863196 MeRIP-seq:(Medium) rs1557198243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5411111,Human_RBP_ID_22692865 Human_Splice_Rec_2248838 97071 RMVar_ID_97071 Human_SNP_ID_735993804 m1A Human chrX - 154439043 154439043 154439043 CTGCCCTCCACCACCTTGAAGTCCAGGTAGCGAGTCACCTCTGTATACAGTAGCATCTTTACCAG CTGCCCTCCACCACCTTGAAGTCCAGGTAGCGGGTCACCTCTGTATACAGTAGCATCTTTACCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154439007..154439080 26863196 MeRIP-seq:(Medium) rs1418744543 Functional Loss SNV dbSNP153 33..33 33 - - - 97072 RMVar_ID_97072 Human_SNP_ID_735994089 m1A Human chrX + 154440127 154440127 154440127 CATCGATTTCACTGGCCATGCCCTGGCGCTCTACCGCACTGATGAGTGAGGGGAAGCTGGGTGGT CATCGATTTCACTGGCCATGCCCTGGCGCTCTGCCGCACTGATGAGTGAGGGGAAGCTGGGTGGT A G GDI1 Ensembl:ENSG00000203879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154439924..154440300 26863196 MeRIP-seq:(Medium) rs782348055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24335152,Human_RBP_ID_26835229 Human_Splice_Rec_2248853 Human_miRNA_ID_2769537 RMVar_hsa_circ_52603 97073 RMVar_ID_97073 Human_SNP_ID_735994629 m1A Human chrX + 154442249 154442249 154442249 GGAGCCGGCTCTGGAGCTGTTGGAGCCCATTGACCAGAAGTGAGGGACTGGGCTGAGCCCAAGGG GGAGCCGGCTCTGGAGCTGTTGGAGCCCATTGTCCAGAAGTGAGGGACTGGGCTGAGCCCAAGGG A T GDI1 Ensembl:ENSG00000203879 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154442201..154442250 26863196 MeRIP-seq:(Medium) rs782346555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799985,Human_RBP_ID_848710 Human_Splice_Rec_2248861,Human_Splice_Rec_2248913,Human_Splice_Rec_2248919,Human_Splice_Rec_2248923 RMVar_hsa_circ_22989,RMVar_hsa_circ_264517,RMVar_hsa_circ_309394,RMVar_hsa_circ_96968 97074 RMVar_ID_97074 Human_SNP_ID_735994732 m1A Human chrX - 154442653 154442653 154442653 GGGGCGGCCACAATCACTGCTCAGCTTCTCCAAAGACGTCGTTCTGTTTGCGCTTCATGTTCTCA GGGGCGGCCACAATCACTGCTCAGCTTCTCCAGAGACGTCGTTCTGTTTGCGCTTCATGTTCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154442602..154442925 26863196 MeRIP-seq:(Medium) rs782788866 Functional Loss SNV dbSNP153 33..33 33 - - - 97075 RMVar_ID_97075 Human_SNP_ID_735994733 m1A Human chrX + 154442665 154442665 154442665 GCGCAAACAGAACGACGTCTTTGGAGAAGCTGAGCAGTGATTGTGGCCGCCCCCAGCCCCTGCTG GCGCAAACAGAACGACGTCTTTGGAGAAGCTGTGCAGTGATTGTGGCCGCCCCCAGCCCCTGCTG A T GDI1 Ensembl:ENSG00000203879 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154442614..154442800 26863196 MeRIP-seq:(Medium) rs781807167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731822,Human_RBP_ID_1061682,Human_RBP_ID_7987491,Human_RBP_ID_16849950,Human_RBP_ID_17553595,Human_RBP_ID_24335163 Human_miRNA_ID_2389137,Human_miRNA_ID_2686786 RMVar_hsa_circ_264517,RMVar_hsa_circ_96968,RMVar_hsa_circ_103088,RMVar_hsa_circ_112666,RMVar_hsa_circ_264518,RMVar_hsa_circ_264519 97076 RMVar_ID_97076 Human_SNP_ID_735995179 m1A Human chrX - 154444232 154444208 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGC________________________GGCGGGCGG CGCCGCCGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs1445180152 Functional Loss DEL dbSNP153 33..56 33 - - - 97077 RMVar_ID_97077 Human_SNP_ID_735995188 m1A Human chrX - 154444232 154444214 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGC__________________GGCGGCGGCGGGCGG CGCCGCCGCCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs782200296 Functional Loss DEL dbSNP153 33..50 33 - - - 97078 RMVar_ID_97078 Human_SNP_ID_735995196 m1A Human chrX - 154444232 154444223 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGC_________GGCGGCGGCGGCGGCGGCGGGCGG CGCCGCCGCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs1456364844 Functional Loss DEL dbSNP153 33..41 33 - - - 97079 RMVar_ID_97079 Human_SNP_ID_735995197 m1A Human chrX - 154444232 154444226 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGC______GGCGGCGGCGGCGGCGGCGGCGGGCGG CGCCGCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs782314598 Functional Loss DEL dbSNP153 33..38 33 - - - 97080 RMVar_ID_97080 Human_SNP_ID_735995200 m1A Human chrX - 154444232 154444229 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGC___GGCGGCGGCGGCGGCGGCGGCGGCGGGCGG CGCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs782686424 Functional Loss DEL dbSNP153 33..35 33 - - - 97081 RMVar_ID_97081 Human_SNP_ID_735995204 m1A Human chrX - 154444232 154444232 154444232 TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG TCGCTCGCGGCGCCCTTGTATTGAGCCATGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154444176..154444275 26863196 MeRIP-seq:(Medium) rs782344035 Functional Loss SNV dbSNP153 33..33 33 - - - 97082 RMVar_ID_97082 Human_SNP_ID_735995205 m1A Human chrX - 154444245 154444245 154444245 GGCGCGGCCGGCCTCGCTCGCGGCGCCCTTGTATTGAGCCATGGCAGCGGCGGCGGCGGCGGCGG GGCGCGGCCGGCCTCGCTCGCGGCGCCCTTGTGTTGAGCCATGGCAGCGGCGGCGGCGGCGGCGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chrX:154444151..154444485;chrX:154444151..154444350 26863410 MeRIP-seq:(Medium) rs1354744813 Functional Loss SNV dbSNP153 33..33 33 - - - 97083 RMVar_ID_97083 Human_SNP_ID_735996265 m1A Human chrX + 154449207 154449197 154449208 GCAGGCTTCCGCCTTCCCTTCCCAACTCCTGGATTCCCGGATACAGATGAGAAAGGGCAACACCA GCAGGCTTCCGCCTTCCCTTCCC___________TCCCGGATACAGATGAGAAAGGGCAACACCA CAACTCCTGGAT C FAM50A Ensembl:ENSG00000071859 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154449201..154449250 26863196 MeRIP-seq:(Medium) rs782339115 Functional Loss DEL dbSNP153 24..34 33 - - - Human_Splice_Rec_2248938,Human_Splice_Rec_2248962,Human_Splice_Rec_2248996 RMVar_hsa_circ_22639,RMVar_hsa_circ_57134,RMVar_hsa_circ_107813,RMVar_hsa_circ_264522,RMVar_hsa_circ_111591,RMVar_hsa_circ_264520,RMVar_hsa_circ_90392,RMVar_hsa_circ_83895,RMVar_hsa_circ_264521,RMVar_hsa_circ_355459,RMVar_hsa_circ_264523,RMVar_hsa_circ_109234,RMVar_hsa_circ_124294,RMVar_hsa_circ_113037,RMVar_hsa_circ_115847,RMVar_hsa_circ_264524,RMVar_hsa_circ_264525,RMVar_hsa_circ_264526,RMVar_hsa_circ_264528,RMVar_hsa_circ_100197,RMVar_hsa_circ_264527 97084 RMVar_ID_97084 Human_SNP_ID_735996349 m1A Human chrX - 154449517 154449517 154449517 ATGGTTTAGTGAGCACAGGACTGGCGCCCAGCACCCTCCACCTTTGGGCTAAGGAACCAAGGCAG ATGGTTTAGTGAGCACAGGACTGGCGCCCAGCGCCCTCCACCTTTGGGCTAAGGAACCAAGGCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154449201..154449950 26863196 MeRIP-seq:(Medium) rs1201504646 Functional Loss SNV dbSNP153 33..33 33 - - - 97085 RMVar_ID_97085 Human_SNP_ID_735998522 m1A Human chrX + 154458657 154458657 154458657 TTGTCGCAGGGGAGCGGCCCCTCGGAGGATCAACGCTGTACTTCCCTCCCGCTAAGGGCTCCGCG TTGTCGCAGGGGAGCGGCCCCTCGGAGGATCAGCGCTGTACTTCCCTCCCGCTAAGGGCTCCGCG A G PLXNA3 Ensembl:ENSG00000130827 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154458625..154458787 26863196 MeRIP-seq:(Medium) rs1409258532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5330621,Human_RBP_ID_21811490,Human_RBP_ID_24539433 97086 RMVar_ID_97086 Human_SNP_ID_735999909 m1A Human chrX - 154462190 154462190 154462190 CTGTCGGCCAGCAGGGGCAGCCCCTCGATCACATGCAGGCCTCCCAGAGGCTGGTTCAACACCAG CTGTCGGCCAGCAGGGGCAGCCCCTCGATCACGTGCAGGCCTCCCAGAGGCTGGTTCAACACCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154461624..154464204 32194978 MeRIP-seq:(Medium) rs1557204936 Functional Loss SNV dbSNP153 33..33 33 - - - 97087 RMVar_ID_97087 Human_SNP_ID_736001139 m1A Human chrX + 154465792 154465792 154465792 GCTGCGGACCCACTGCCCGGCCCCGAAGACCAACTGGATGCACCTGAGCCAGAAGGGCACCCGGT GCTGCGGACCCACTGCCCGGCCCCGAAGACCAGCTGGATGCACCTGAGCCAGAAGGGCACCCGGT A G PLXNA3 Ensembl:ENSG00000130827 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154465743..154465894 26863196 MeRIP-seq:(Medium) rs929475680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2249035 RMVar_hsa_circ_120011,RMVar_hsa_circ_90039,RMVar_hsa_circ_84592,RMVar_hsa_circ_117993,RMVar_hsa_circ_264533,RMVar_hsa_circ_264534,RMVar_hsa_circ_264535,RMVar_hsa_circ_121484,RMVar_hsa_circ_125030,RMVar_hsa_circ_264536,RMVar_hsa_circ_264537,RMVar_hsa_circ_123395,RMVar_hsa_circ_264538,RMVar_hsa_circ_22717,RMVar_hsa_circ_115673,RMVar_hsa_circ_264539,RMVar_hsa_circ_264540 97088 RMVar_ID_97088 Human_SNP_ID_736001444 m1A Human chrX + 154466744 154466744 154466744 ACATCTCCAGCCCCGGGCTCATCTACACCTACACTCAGGACCCCACCGTCACCCGCCTTGAGCCC ACATCTCCAGCCCCGGGCTCATCTACACCTACTCTCAGGACCCCACCGTCACCCGCCTTGAGCCC A T PLXNA3 Ensembl:ENSG00000130827 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154466694..154466781 26863196 MeRIP-seq:(Medium) rs1557207291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186601,Human_RBP_ID_23099774,Human_RBP_ID_27834265 Human_Splice_Rec_2249043,Human_Splice_Rec_2249085 RMVar_hsa_circ_120011,RMVar_hsa_circ_90039,RMVar_hsa_circ_84592,RMVar_hsa_circ_117993,RMVar_hsa_circ_264533,RMVar_hsa_circ_264534,RMVar_hsa_circ_264535,RMVar_hsa_circ_121484,RMVar_hsa_circ_125030,RMVar_hsa_circ_264536,RMVar_hsa_circ_264537,RMVar_hsa_circ_123395,RMVar_hsa_circ_264538,RMVar_hsa_circ_115673,RMVar_hsa_circ_264539,RMVar_hsa_circ_264540 97089 RMVar_ID_97089 Human_SNP_ID_736004298 m1A Human chrX - 154477976 154477976 154477976 TTCTTGACCAGCTTTCCCTGGTGGTGCGGACCATGCAGCGCTTTGGGCCCCCCGTTTCCCGCTAA TTCTTGACCAGCTTTCCCTGGTGGTGCGGACCGTGCAGCGCTTTGGGCCCCCCGTTTCCCGCTAA T C LAGE3 Ensembl:ENSG00000196976 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154477926..154478300 26863196 MeRIP-seq:(Medium) rs1461742307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731883,Human_RBP_ID_1061693,Human_RBP_ID_5058164,Human_RBP_ID_9340108,Human_RBP_ID_16850098,Human_RBP_ID_17667377,Human_RBP_ID_18197523,Human_RBP_ID_22469049,Human_RBP_ID_24335237 Human_Splice_Rec_2249106 97090 RMVar_ID_97090 Human_SNP_ID_736004430 m1A Human chrX - 154478413 154478413 154478413 GTATCAGATGGCACCTTAACCGAATGACCCCCAGCACCCTCAGCGTGCCTTTCCCGACCCCCTTG GTATCAGATGGCACCTTAACCGAATGACCCCCGGCACCCTCAGCGTGCCTTTCCCGACCCCCTTG T C LAGE3 Ensembl:ENSG00000196976 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154478376..154478425 26863196 MeRIP-seq:(Medium) rs782344105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967102,Human_RBP_ID_22485049 97091 RMVar_ID_97091 Human_SNP_ID_736006032 m1A Human chrX - 154485868 154485868 154485868 ACTAGAAGAAGGCGAGGCCCAGAGGCTGGCCGACTCCCCACCCCCGCAGGTCTGGCAGCTGATCT ACTAGAAGAAGGCGAGGCCCAGAGGCTGGCCGCCTCCCCACCCCCGCAGGTCTGGCAGCTGATCT T G UBL4A Ensembl:ENSG00000102178 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154485776..154486015 26863196 MeRIP-seq:(Medium) rs782643777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076879,Human_RBP_ID_8944834,Human_RBP_ID_27550892 Human_Splice_Rec_2249111,Human_Splice_Rec_2249115,Human_Splice_Rec_2249121,Human_Splice_Rec_2249125,Human_Splice_Rec_2249131 Human_miRNA_ID_635138,Human_miRNA_ID_2368643,Human_miRNA_ID_2726933,Human_miRNA_ID_3016422 RMVar_hsa_circ_3878,RMVar_hsa_circ_105199,RMVar_hsa_circ_264548,RMVar_hsa_circ_76088,RMVar_hsa_circ_264547 97092 RMVar_ID_97092 Human_SNP_ID_736006037 m1A Human chrX - 154485880 154485880 154485880 GGAGAAGGTGCTACTAGAAGAAGGCGAGGCCCAGAGGCTGGCCGACTCCCCACCCCCGCAGGTCT GGAGAAGGTGCTACTAGAAGAAGGCGAGGCCCGGAGGCTGGCCGACTCCCCACCCCCGCAGGTCT T C UBL4A Ensembl:ENSG00000102178 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154485830..154485896 26863196 MeRIP-seq:(Medium) rs1557212746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5058305,Human_RBP_ID_8944834 Human_Splice_Rec_2249110,Human_Splice_Rec_2249114,Human_Splice_Rec_2249120,Human_Splice_Rec_2249134 Human_miRNA_ID_2368643,Human_miRNA_ID_2398826,Human_miRNA_ID_2426062,Human_miRNA_ID_2435733,Human_miRNA_ID_2726933 RMVar_hsa_circ_3878,RMVar_hsa_circ_105199,RMVar_hsa_circ_264548,RMVar_hsa_circ_76088,RMVar_hsa_circ_264547 97093 RMVar_ID_97093 Human_SNP_ID_736006273 m1A Human chrX + 154486620 154486620 154486620 GGTCGCGACGGCGTCCACTCGGGCCGGCGCGCACCCCAACCACCCCCCGCCGCGCGCCGCCGCCC GGTCGCGACGGCGTCCACTCGGGCCGGCGCGCCCCCCAACCACCCCCCGCCGCGCGCCGCCGCCC A C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:154486317..154486620 26863410 MeRIP-seq:(Medium) rs1557213011 Functional Loss SNV dbSNP153 33..33 33 - - - 97094 RMVar_ID_97094 Human_SNP_ID_736006277 m1A Human chrX + 154486629 154486629 154486629 GGCGTCCACTCGGGCCGGCGCGCACCCCAACCACCCCCCGCCGCGCGCCGCCGCCCCGGGCGCGC GGCGTCCACTCGGGCCGGCGCGCACCCCAACCCCCCCCCGCCGCGCGCCGCCGCCCCGGGCGCGC A C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:154486589..154486671 26863410 MeRIP-seq:(Medium) rs781978879 Functional Loss SNV dbSNP153 33..33 33 - - - 97095 RMVar_ID_97095 Human_SNP_ID_736011103 m1A Human chrX - 154506885 154506885 154506885 CCTCCCCACAGCACGTGAAGAACAGTAAGCACAGCAACAAGTACGAAGGCTGGCCCGAGGCGCTG CCTCCCCACAGCACGTGAAGAACAGTAAGCACGGCAACAAGTACGAAGGCTGGCCCGAGGCGCTG T C FAM3A Ensembl:ENSG00000071889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154506530..154506925 26863196 MeRIP-seq:(Medium) rs953850219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977856 Human_Splice_Rec_2249174,Human_Splice_Rec_2249188,Human_Splice_Rec_2249208,Human_Splice_Rec_2249224,Human_Splice_Rec_2249236,Human_Splice_Rec_2249253,Human_Splice_Rec_2249263,Human_Splice_Rec_2249278,Human_Splice_Rec_2249294,Human_Splice_Rec_2249309,Human_Splice_Rec_2249311 97096 RMVar_ID_97096 Human_SNP_ID_736011308 m1A Human chrX + 154507487 154507487 154507487 GCAGTGGCCGAATAAACTTCAACAGGTCGTTGACATCTGGGGGGGCAGGTGCCACGGAACAGGGG GCAGTGGCCGAATAAACTTCAACAGGTCGTTGTCATCTGGGGGGGCAGGTGCCACGGAACAGGGG A T RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154507378..154507509 26863196 MeRIP-seq:(Medium) rs782495251 Functional Loss SNV dbSNP153 33..33 33 - - - 97097 RMVar_ID_97097 Human_SNP_ID_736012479 m1A Human chrX - 154512856 154512856 154512856 TCGTGGTCAGCATCCTCCTGGGTGGGCCTGGCAGTGGCTTTCCTCGCATCCAGCAACTCTTCACC TCGTGGTCAGCATCCTCCTGGGTGGGCCTGGCGGTGGCTTTCCTCGCATCCAGCAACTCTTCACC T C FAM3A Ensembl:ENSG00000071889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154511400..154512950 26863196 MeRIP-seq:(Medium) rs782791470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731949,Human_RBP_ID_799142,Human_RBP_ID_967679,Human_RBP_ID_3977045,Human_RBP_ID_18148079 Human_Splice_Rec_2249160,Human_Splice_Rec_2249161,Human_Splice_Rec_2249176,Human_Splice_Rec_2249177,Human_Splice_Rec_2249192,Human_Splice_Rec_2249193,Human_Splice_Rec_2249211,Human_Splice_Rec_2249212,Human_Splice_Rec_2249226,Human_Splice_Rec_2249227,Human_Splice_Rec_2249238,Human_Splice_Rec_2249239,Human_Splice_Rec_2249265,Human_Splice_Rec_2249266,Human_Splice_Rec_2249281,Human_Splice_Rec_2249282,Human_Splice_Rec_2249315,Human_Splice_Rec_2249316,Human_Splice_Rec_2249333,Human_Splice_Rec_2249334,Human_Splice_Rec_2249347,Human_Splice_Rec_2249348,Human_Splice_Rec_2249359,Human_Splice_Rec_2249360,Human_Splice_Rec_2249367,Human_Splice_Rec_2249368,Human_Splice_Rec_2249382,Human_Splice_Rec_2249383,Human_Splice_Rec_2249400,Human_Splice_Rec_2249401,Human_Splice_Rec_2249406,Human_Splice_Rec_2249407 RMVar_hsa_circ_44702,RMVar_hsa_circ_329661,RMVar_hsa_circ_264552 97098 RMVar_ID_97098 Human_SNP_ID_736012486 m1A Human chrX + 154512873 154512873 154512873 TGCGAGGAAAGCCACTGCCAGGCCCACCCAGGAGGATGCTGACCACGATCCATGTGACACCCACA TGCGAGGAAAGCCACTGCCAGGCCCACCCAGGCGGATGCTGACCACGATCCATGTGACACCCACA A C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:154512427..154515938;chrX:154512781..154512978;chrX:154512765..154512900 26863196 MeRIP-seq:(Medium) rs1259515234 Functional Loss SNV dbSNP153 33..33 33 - - - 97099 RMVar_ID_97099 Human_SNP_ID_736012487 m1A Human chrX + 154512873 154512873 154512873 TGCGAGGAAAGCCACTGCCAGGCCCACCCAGGAGGATGCTGACCACGATCCATGTGACACCCACA TGCGAGGAAAGCCACTGCCAGGCCCACCCAGGTGGATGCTGACCACGATCCATGTGACACCCACA A T RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:154512427..154515938;chrX:154512781..154512978;chrX:154512765..154512900 26863196 MeRIP-seq:(Medium) rs1259515234 Functional Loss SNV dbSNP153 33..33 33 - - - 97100 RMVar_ID_97100 Human_SNP_ID_736017386 m1A Human chrX + 154532701 154532701 154532701 CTGCACGCGGATCACCAGCTCGTTGCGCTTGCACTGCTGGTGGAAGATGTCGCCGGCCACATCAT CTGCACGCGGATCACCAGCTCGTTGCGCTTGCGCTGCTGGTGGAAGATGTCGCCGGCCACATCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154532549..154532829 26863196 MeRIP-seq:(Medium) rs137852322 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_585 97101 RMVar_ID_97101 Human_SNP_ID_736017910 m1A Human chrX - 154534440 154534440 154534440 GAAGCCCTTCGGGAGGGACCTGCAGAGCTCTGACCGGCTGTCCAACCACATCTCCTCCCTGTTCC GAAGCCCTTCGGGAGGGACCTGCAGAGCTCTGTCCGGCTGTCCAACCACATCTCCTCCCTGTTCC T A G6PD Ensembl:ENSG00000160211 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154534140..154534500 32194978 MeRIP-seq:(Medium) rs5030872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799743,Human_RBP_ID_5230753,Human_RBP_ID_22469055,Human_RBP_ID_27550954 Human_Splice_Rec_2249420,Human_Splice_Rec_2249444,Human_Splice_Rec_2249468,Human_Splice_Rec_2249496,Human_Splice_Rec_2249512,Human_Splice_Rec_2249530 Clinvar_Rec_586,Clinvar_Rec_5476 GWAS_ID_12776,GWAS_ID_12777 RMVar_hsa_circ_97331,RMVar_hsa_circ_128070,RMVar_hsa_circ_78607,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553,RMVar_hsa_circ_100622,RMVar_hsa_circ_94632,RMVar_hsa_circ_264565,RMVar_hsa_circ_81677,RMVar_hsa_circ_264567,RMVar_hsa_circ_84762,RMVar_hsa_circ_264566,RMVar_hsa_circ_89369,RMVar_hsa_circ_264568,RMVar_hsa_circ_264569,RMVar_hsa_circ_264572,RMVar_hsa_circ_127465,RMVar_hsa_circ_264573,RMVar_hsa_circ_275563 97102 RMVar_ID_97102 Human_SNP_ID_736018112 m1A Human chrX - 154535220 154535220 154535220 CCAACCGCCTCTTCTACCTGGCCTTGCCCCCGACCGTCTACGAGGCCGTCACCAAGAACATTCAC CCAACCGCCTCTTCTACCTGGCCTTGCCCCCGTCCGTCTACGAGGCCGTCACCAAGAACATTCAC T A G6PD Ensembl:ENSG00000160211 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:154535124..154535423;chrX:154535135..154535334 26863196 MeRIP-seq:(Medium) rs782264331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9409595,Human_RBP_ID_18197531 Human_Splice_Rec_2249419,Human_Splice_Rec_2249443,Human_Splice_Rec_2249467,Human_Splice_Rec_2249495,Human_Splice_Rec_2249511,Human_Splice_Rec_2249529 RMVar_hsa_circ_97331,RMVar_hsa_circ_128070,RMVar_hsa_circ_78607,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553,RMVar_hsa_circ_100622,RMVar_hsa_circ_86302,RMVar_hsa_circ_264565,RMVar_hsa_circ_264567,RMVar_hsa_circ_84762,RMVar_hsa_circ_264575,RMVar_hsa_circ_76117,RMVar_hsa_circ_264574 97103 RMVar_ID_97103 Human_SNP_ID_736020362 m1A Human chrX + 154546121 154546121 154546121 CCTGGAAAAGCTCTTCCCGCAGGATCCCGCACACCTGGGTCCGGCTCAGGGCCACCTGCTCTGCC CCTGGAAAAGCTCTTCCCGCAGGATCCCGCACCCCTGGGTCCGGCTCAGGGCCACCTGCTCTGCC A C IKBKG Ensembl:ENSG00000269335 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154546071..154546171 32194978 MeRIP-seq:(Medium) rs1205973162 Functional Loss SNV dbSNP153 33..33 33 - - - 97104 RMVar_ID_97104 Human_SNP_ID_736020485 m1A Human chrX + 154546701 154546701 154546701 AAGACCCTCTCGATTCTGCTCGGTTCTCAAGCACAACAAACAGCGTGTATTTTACCGCCGCGCGG AAGACCCTCTCGATTCTGCTCGGTTCTCAAGCCCAACAAACAGCGTGTATTTTACCGCCGCGCGG A C IKBKG Ensembl:ENSG00000269335 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154546698..154546850 26863196 MeRIP-seq:(Medium) rs1230463520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3247603,Human_RBP_ID_22705385 97105 RMVar_ID_97105 Human_SNP_ID_736021756 m1A Human chrX - 154552098 154552098 154552098 GAAGGCAGGTGCAGCATGGCTGGCTTCCCCAGAGGAGACTCTTCGCCCAGTACGTCCTGATCTGC GAAGGCAGGTGCAGCATGGCTGGCTTCCCCAGTGGAGACTCTTCGCCCAGTACGTCCTGATCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154552047..154552121 26863196 MeRIP-seq:(Medium) rs1451683583 Functional Loss SNV dbSNP153 33..33 33 - - - 97106 RMVar_ID_97106 Human_SNP_ID_736048525 m1A Human chrX - 154762917 154762917 154762917 TGCGTGCCGCCCGGTCCACAGCCGAGGGAACGACCGCAGACTCCCGCCGCCTTGGTCCCGTCAGG TGCGTGCCGCCCGGTCCACAGCCGAGGGAACGGCCGCAGACTCCCGCCGCCTTGGTCCCGTCAGG T C lnc-GAB3-3,lnc-GAB3-3:2 RNACentral:URS0000D5705E,RNACentral:URS0000D577DB lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:154762825..154763063;chrX:154762804..154763064;chrX:154762782..154763059;chrX:154762833..154763055 26863196 MeRIP-seq:(Medium) rs1557263710 Functional Loss SNV dbSNP153 33..33 33 - - - 97107 RMVar_ID_97107 Human_SNP_ID_736049183 m1A Human chrX + 154765964 154765964 154765964 CAACACACTATACACCTCTTGCATGTGGTTCAAATCCTCTGAAGAGAGAGATTGGGGACTATATC CAACACACTATACACCTCTTGCATGTGGTTCAGATCCTCTGAAGAGAGAGATTGGGGACTATATC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1178002753 Functional Loss SNV dbSNP153 33..33 33 - - - 97108 RMVar_ID_97108 Human_SNP_ID_736049667 m1A Human chrX - 154768370 154768370 154768370 CCGAAGCTCCTGCATCTGACCACCAACTCCCAATAACAAACCAAGGTGCACACATAATGTCCGAA CCGAAGCTCCTGCATCTGACCACCAACTCCCAGTAACAAACCAAGGTGCACACATAATGTCCGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154768303..154768464 26863196 MeRIP-seq:(Medium) rs1557264481 Functional Loss SNV dbSNP153 33..33 33 - - - 97109 RMVar_ID_97109 Human_SNP_ID_736050621 m1A Human chrX - 154773243 154773243 154773243 AGGGCACGCAACCCAGTACCACTTACCTTTGGACCTAAACCCCACTTCCGAGGGTAAGTGTCTCT AGGGCACGCAACCCAGTACCACTTACCTTTGGGCCTAAACCCCACTTCCGAGGGTAAGTGTCTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154773194..154773281 26863196 MeRIP-seq:(Medium) rs2853355 Functional Loss SNV dbSNP153 33..33 33 - - - 97110 RMVar_ID_97110 Human_SNP_ID_736099233 m1A Human chrX - 155071104 155071104 155071104 GTACTCTGTGAGCGGCGCCCGGGCGCCTGGGCAGGCGCCTCCCGAGTACCGGCGCCCATTTTGCC GTACTCTGTGAGCGGCGCCCGGGCGCCTGGGCGGGCGCCTCCCGAGTACCGGCGCCCATTTTGCC T C CMC4,MTCP1 Ensembl:ENSG00000182712,Ensembl:ENSG00000214827 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:155070905..155071213 26863410 MeRIP-seq:(Medium) rs1304384460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076436 97111 RMVar_ID_97111 Human_SNP_ID_736099234 m1A Human chrX - 155071104 155071104 155071104 GTACTCTGTGAGCGGCGCCCGGGCGCCTGGGCAGGCGCCTCCCGAGTACCGGCGCCCATTTTGCC GTACTCTGTGAGCGGCGCCCGGGCGCCTGGGCCGGCGCCTCCCGAGTACCGGCGCCCATTTTGCC T G CMC4,MTCP1 Ensembl:ENSG00000182712,Ensembl:ENSG00000214827 Protein coding,Protein coding 5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:155070905..155071213 26863410 MeRIP-seq:(Medium) rs1304384460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076436 97112 RMVar_ID_97112 Human_SNP_ID_736124357 m1A Human chrX - 155216568 155216568 155216568 TGCCAGGGAACAGCGTGCCTCTTACCACAAACACGGCCTCAGGAATCCCCAGGTGGAGCCGCCGC TGCCAGGGAACAGCGTGCCTCTTACCACAAACTCGGCCTCAGGAATCCCCAGGTGGAGCCGCCGC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:155216518..155228388 32194978 MeRIP-seq:(Medium) rs1557309039 Functional Loss SNV dbSNP153 33..33 33 - - - 97113 RMVar_ID_97113 Human_SNP_ID_736124359 m1A Human chrX - 155216577 155216576 155216577 AAGCCAAGATGCCAGGGAACAGCGTGCCTCTTACCACAAACACGGCCTCAGGAATCCCCAGGTGG AAGCCAAGATGCCAGGGAACAGCGTGCCTCTT_CCACAAACACGGCCTCAGGAATCCCCAGGTGG GT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chrX:155216478..155220224;chrX:155216557..155216663 26863410,32194978 MeRIP-seq:(Medium) rs782675292 Functional Loss DEL dbSNP153 33..33 33 - - - 97114 RMVar_ID_97114 Human_SNP_ID_736124876 m1A Human chrX + 155220141 155220141 155220141 TAAAAACAAAGCAGTCAAAAAATCTGAGTGGCATGAATTCTAAAATTTGTAAAGTATTATTTTTG TAAAAACAAAGCAGTCAAAAAATCTGAGTGGCGTGAATTCTAAAATTTGTAAAGTATTATTTTTG A G VBP1 Ensembl:ENSG00000155959 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:155220138..155220250;chrX:155220139..155220325 26863196 MeRIP-seq:(Medium) rs981576393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65237 97115 RMVar_ID_97115 Human_SNP_ID_736269316 m1A Human chrX - 156009139 156009131 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACA________CACAAACATACACAGACACATAAAC GTGTGTGTT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1180622243 Functional Loss DEL dbSNP153 33..40 33 - - - 97116 RMVar_ID_97116 Human_SNP_ID_736269319 m1A Human chrX - 156009139 156009133 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACA______CACACAAACATACACAGACACATAAAC GTGTGTT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1438333771 Functional Loss DEL dbSNP153 33..38 33 - - - 97117 RMVar_ID_97117 Human_SNP_ID_736269320 m1A Human chrX - 156009139 156009135 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACA____CACACACAAACATACACAGACACATAAAC GTGTT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1316146242 Functional Loss DEL dbSNP153 33..36 33 - - - 97118 RMVar_ID_97118 Human_SNP_ID_736269322 m1A Human chrX - 156009139 156009137 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACA__CACACACACAAACATACACAGACACATAAAC GTT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1251951165 Functional Loss DEL dbSNP153 33..34 33 - - - 97119 RMVar_ID_97119 Human_SNP_ID_736269328 m1A Human chrX - 156009139 156009139 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACAGACACACACACAAACATACACAGACACATAAAC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1279795380 Functional Loss SNV dbSNP153 33..33 33 - - - 97120 RMVar_ID_97120 Human_SNP_ID_736269329 m1A Human chrX - 156009139 156009139 156009139 CATACACACATAAACACAAACACACACACACAAACACACACACAAACATACACAGACACATAAAC CATACACACATAAACACAAACACACACACACACACACACACACAAACATACACAGACACATAAAC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:156008882..156009399 26863196 MeRIP-seq:(Medium) rs1279795380 Functional Loss SNV dbSNP153 33..33 33 - - - 97121 RMVar_ID_97121 Human_SNP_ID_736273099 m1A Human chrX + 156023162 156023162 156023162 GCCCCGGCATTGCCCCCTCTGCCCCTGGCACCATTCCGGAACTGCCCACCTTCCACACTGAGGTA GCCCCGGCATTGCCCCCTCTGCCCCTGGCACCCTTCCGGAACTGCCCACCTTCCACACTGAGGTA A C WASH6P Ensembl:ENSG00000182484 Pseudogene exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:156023063..156023200 26863196 MeRIP-seq:(Medium) rs1196185107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977060,Human_RBP_ID_5638066,Human_RBP_ID_8715908,Human_RBP_ID_9410259,Human_RBP_ID_23259839,Human_RBP_ID_26364385 Human_Splice_Rec_2250660,Human_Splice_Rec_2250681,Human_Splice_Rec_2250707,Human_Splice_Rec_2250730 97122 RMVar_ID_97122 Human_SNP_ID_736273100 m1A Human chrX + 156023162 156023162 156023162 GCCCCGGCATTGCCCCCTCTGCCCCTGGCACCATTCCGGAACTGCCCACCTTCCACACTGAGGTA GCCCCGGCATTGCCCCCTCTGCCCCTGGCACCGTTCCGGAACTGCCCACCTTCCACACTGAGGTA A G WASH6P Ensembl:ENSG00000182484 Pseudogene exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:156023063..156023200 26863196 MeRIP-seq:(Medium) rs1196185107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977060,Human_RBP_ID_5638066,Human_RBP_ID_8715908,Human_RBP_ID_9410259,Human_RBP_ID_23259839,Human_RBP_ID_26364385 Human_Splice_Rec_2250660,Human_Splice_Rec_2250681,Human_Splice_Rec_2250707,Human_Splice_Rec_2250730 97123 RMVar_ID_97123 Human_SNP_ID_55507513 m1A Human chr1 + 240092411 240092411 240092411 CGGCGGCTCCCGCGAAGATGTACTGGATTCCCAGGCCCTGCAGACCGGGGAGCTGGACAGCGCTC CGGCGGCTCCCGCGAAGATGTACTGGATTCCCCGGCCCTGCAGACCGGGGAGCTGGACAGCGCTC A C FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:240092294..240092495 32194978 MeRIP-seq:(Medium) rs879159241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_347821,Human_RBP_ID_1425740 97124 RMVar_ID_97124 Human_SNP_ID_55507616 m1A Human chr1 - 240092644 240092644 240092644 AGCCGAATGGAAGCTATAGATGTCCGTGTCCGAGCCCGAGCTGGTCCTTTGTCCATCCTGCGCCC AGCCGAATGGAAGCTATAGATGTCCGTGTCCGCGCCCGAGCTGGTCCTTTGTCCATCCTGCGCCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:240092594..240092795 32194978 MeRIP-seq:(Medium) rs1444404140 Functional Loss SNV dbSNP153 33..33 33 - - - 97125 RMVar_ID_97125 Human_SNP_ID_55508333 m1A Human chr1 + 240094533 240094531 240094533 ATACCCAGGGCGGCATAAAGCACAGCCAGAGTATGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT ATACCCAGGGCGGCATAAAGCACAGCCAGAG__TGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT GTA G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1479825906 Functional Loss DEL dbSNP153 32..33 33 - - - 97126 RMVar_ID_97126 Human_SNP_ID_55508334 m1A Human chr1 + 240094533 240094533 240094533 ATACCCAGGGCGGCATAAAGCACAGCCAGAGTATGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT ATACCCAGGGCGGCATAAAGCACAGCCAGAGTGTGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT A G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs55746338 Functional Loss SNV dbSNP153 33..33 33 - - - 97127 RMVar_ID_97127 Human_SNP_ID_55520806 m1A Human chr1 + 240145239 240145235 240145239 CAGTTCATCTTGAAGCTGTTTATCTTCCTCAGACAGCTCCTGTTCTTTGTCCTTGTCCCCGGCAT CAGTTCATCTTGAAGCTGTTTATCTTCCT____CAGCTCCTGTTCTTTGTCCTTGTCCCCGGCAT TCAGA T FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:240145189..240145298 26863196 MeRIP-seq:(Medium) rs1342282550 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_89051,RMVar_hsa_circ_305988,RMVar_hsa_circ_328270,RMVar_hsa_circ_302723,RMVar_hsa_circ_141023,RMVar_hsa_circ_141024 97128 RMVar_ID_97128 Human_SNP_ID_55528357 m1A Human chr1 + 240173515 240173498 240173515 CAGGTGAAATGGGACTTCAACTAGATTTTTTAATGATTGATTAGACTCCTTGAGTGGGTAGAGCT CAGGTGAAATGGGACT_________________TGATTGATTAGACTCCTTGAGTGGGTAGAGCT TTCAACTAGATTTTTTAA T FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:240173453..240173584 26863196 MeRIP-seq:(Medium) rs1222427983 Functional Loss DEL dbSNP153 17..33 33 - - - RMVar_hsa_circ_89051,RMVar_hsa_circ_305988,RMVar_hsa_circ_328270,RMVar_hsa_circ_302723,RMVar_hsa_circ_141026,RMVar_hsa_circ_141023,RMVar_hsa_circ_141024,RMVar_hsa_circ_125025,RMVar_hsa_circ_141029,RMVar_hsa_circ_85028,RMVar_hsa_circ_141027,RMVar_hsa_circ_141028,RMVar_hsa_circ_141030 97129 RMVar_ID_97129 Human_SNP_ID_55538088 m1A Human chr1 - 240208132 240208132 240208132 TGCCCGCTCCGGGTAGAGGGGGCGGAGGAGGTATGCCCACTCCGGGTAGAGGGGGCGGAGGGGGT TGCCCGCTCCGGGTAGAGGGGGCGGAGGAGGTTTGCCCACTCCGGGTAGAGGGGGCGGAGGGGGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:240208032..240208233 32194978 MeRIP-seq:(Medium) rs765059719 Functional Loss SNV dbSNP153 33..33 33 - - - 97130 RMVar_ID_97130 Human_SNP_ID_55550303 m1A Human chr1 + 240255042 240255042 240255042 CTCAGGGCCTGTGCAGGCCGCGGGGTTCTCCCATGGCTACGATTGCAGGAGTCTGTGGTGGAAAT CTCAGGGCCTGTGCAGGCCGCGGGGTTCTCCCCTGGCTACGATTGCAGGAGTCTGTGGTGGAAAT A C FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:240255011..240255111 32194978 MeRIP-seq:(Medium) rs1275475055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46084,RMVar_hsa_circ_109766,RMVar_hsa_circ_338836,RMVar_hsa_circ_347196,RMVar_hsa_circ_113588,RMVar_hsa_circ_141035,RMVar_hsa_circ_141033,RMVar_hsa_circ_141034,RMVar_hsa_circ_302922,RMVar_hsa_circ_325398,RMVar_hsa_circ_10589,RMVar_hsa_circ_294435,RMVar_hsa_circ_343247,RMVar_hsa_circ_312135,RMVar_hsa_circ_23953,RMVar_hsa_circ_141037,RMVar_hsa_circ_141038,RMVar_hsa_circ_294480,RMVar_hsa_circ_361022,RMVar_hsa_circ_47648,RMVar_hsa_circ_141042,RMVar_hsa_circ_141040,RMVar_hsa_circ_86226 97131 RMVar_ID_97131 Human_SNP_ID_55550304 m1A Human chr1 + 240255042 240255042 240255042 CTCAGGGCCTGTGCAGGCCGCGGGGTTCTCCCATGGCTACGATTGCAGGAGTCTGTGGTGGAAAT CTCAGGGCCTGTGCAGGCCGCGGGGTTCTCCCTTGGCTACGATTGCAGGAGTCTGTGGTGGAAAT A T FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:240255011..240255111 32194978 MeRIP-seq:(Medium) rs1275475055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46084,RMVar_hsa_circ_109766,RMVar_hsa_circ_338836,RMVar_hsa_circ_347196,RMVar_hsa_circ_113588,RMVar_hsa_circ_141035,RMVar_hsa_circ_141033,RMVar_hsa_circ_141034,RMVar_hsa_circ_302922,RMVar_hsa_circ_325398,RMVar_hsa_circ_10589,RMVar_hsa_circ_294435,RMVar_hsa_circ_343247,RMVar_hsa_circ_312135,RMVar_hsa_circ_23953,RMVar_hsa_circ_141037,RMVar_hsa_circ_141038,RMVar_hsa_circ_294480,RMVar_hsa_circ_361022,RMVar_hsa_circ_47648,RMVar_hsa_circ_141042,RMVar_hsa_circ_141040,RMVar_hsa_circ_86226 97132 RMVar_ID_97132 Human_SNP_ID_55856191 m1A Human chr1 - 241497967 241497967 241497967 CATATGTCGTCTTTTTATTTTTTCTTCAGGGTATGACAAGGCAGCAAAGATTGCTAAGACAGCAC CATATGTCGTCTTTTTATTTTTTCTTCAGGGTGTGACAAGGCAGCAAAGATTGCTAAGACAGCAC T C FH Ensembl:ENSG00000091483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:241497938..241498010 26863196 MeRIP-seq:(Medium) rs863224010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17222150,Human_RBP_ID_22635185,Human_RBP_ID_24746468 Human_Splice_Rec_205442 Clinvar_Rec_587 97133 RMVar_ID_97133 Human_SNP_ID_55857874 m1A Human chr1 - 241504132 241504132 241504132 ACACTACTGCCTGCAGTCTGATGAAGATAGCAAATGATATTCGATTTTTGGGTTCTGGTCCTCGG ACACTACTGCCTGCAGTCTGATGAAGATAGCAGATGATATTCGATTTTTGGGTTCTGGTCCTCGG T C FH Ensembl:ENSG00000091483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:241504013..241504160 26863196 MeRIP-seq:(Medium) rs775639021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_205437 Human_miRNA_ID_1782120,Human_miRNA_ID_2915360,Human_miRNA_ID_2989355 RMVar_hsa_circ_62661,RMVar_hsa_circ_62778,RMVar_hsa_circ_268703,RMVar_hsa_circ_312676,RMVar_hsa_circ_92290,RMVar_hsa_circ_105614,RMVar_hsa_circ_141076,RMVar_hsa_circ_23884,RMVar_hsa_circ_365166,RMVar_hsa_circ_101299,RMVar_hsa_circ_141078,RMVar_hsa_circ_141080,RMVar_hsa_circ_88521,RMVar_hsa_circ_141079,RMVar_hsa_circ_141077 97134 RMVar_ID_97134 Human_SNP_ID_55861805 m1A Human chr1 - 241519714 241519714 241519714 TTCTACCCAAGCTCCCTCAGCACCATGTACCGAGCACTTCGGCTCCTCGCGCGCTCGCGTCCCCT TTCTACCCAAGCTCCCTCAGCACCATGTACCGCGCACTTCGGCTCCTCGCGCGCTCGCGTCCCCT T G FH Ensembl:ENSG00000091483 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:241519557..241519725 26863196 MeRIP-seq:(Medium) rs941921568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074881,Human_RBP_ID_9270779,Human_RBP_ID_9319484 Human_miRNA_ID_2088535,Human_miRNA_ID_2314373,Human_miRNA_ID_2317535,Human_miRNA_ID_2320689,Human_miRNA_ID_2323843,Human_miRNA_ID_2327016,Human_miRNA_ID_2518223,Human_miRNA_ID_2521397,Human_miRNA_ID_2589886,Human_miRNA_ID_2820590,Human_miRNA_ID_2826725,Human_miRNA_ID_2829875,Human_miRNA_ID_2833996,Human_miRNA_ID_2839364 RMVar_hsa_circ_105614,RMVar_hsa_circ_141077 97135 RMVar_ID_97135 Human_SNP_ID_55887219 m1A Human chr1 + 241624037 241624037 241624037 CTCTATGCTCCAGGCACTGTGGACCCTCTTCCACCTGTCCTGCCTCTCCATGCCAGGCCAGGCAC CTCTATGCTCCAGGCACTGTGGACCCTCTTCCCCCTGTCCTGCCTCTCCATGCCAGGCCAGGCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:241624033..241624174 26863196 MeRIP-seq:(Medium) rs954206445 Functional Loss SNV dbSNP153 33..33 33 - - - 97136 RMVar_ID_97136 Human_SNP_ID_55887275 m1A Human chr1 + 241624265 241624202 241624266 GTCCTGCCTCTCCACGCCAGGCCAGGCACTCTACGCTCCAGACACTGTGGACCCTCTTTCACCTG __________________________________GCTCCAGACACTGTGGACCCTCTTTCACCTG TGCTCCAGACACTGTGGACCCTCTTTCACCTGTCCTGCCTCTCCACGCCAGGCCAGGCACTCTAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:241624263..241624328 26863196 MeRIP-seq:(Medium) rs1558443560 Functional Loss DEL dbSNP153 1..34 33 - - - 97137 RMVar_ID_97137 Human_SNP_ID_55891350 m1A Human chr1 + 241640040 241640040 241640040 TGTTGACCAGGAGGAGGTGAGTGGGAGTGCGGAGCCGCTGGAACTTGTAGTAGAGGACGAGCACC TGTTGACCAGGAGGAGGTGAGTGGGAGTGCGGGGCCGCTGGAACTTGTAGTAGAGGACGAGCACC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:241640001..241640312 26863196 MeRIP-seq:(Medium) rs767035246 Functional Loss SNV dbSNP153 33..33 33 - - - 97138 RMVar_ID_97138 Human_SNP_ID_55946928 m1A Human chr1 + 241866849 241866849 241866849 TTTCCTTTTCTAGCCTGCCCATTCAAGAAGTCATAGTTGGGATGACAAAACATGTCAAAAGTCAG TTTCCTTTTCTAGCCTGCCCATTCAAGAAGTCGTAGTTGGGATGACAAAACATGTCAAAAGTCAG A G EXO1 Ensembl:ENSG00000174371 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs735943 Functional Loss SNV dbSNP153,EGP,HGVD 33..33 33 - - - Human_RBP_ID_1426131,Human_RBP_ID_8746666,Human_RBP_ID_10869628,Human_RBP_ID_18568676,Human_RBP_ID_21908409,Human_RBP_ID_22783236,Human_RBP_ID_23378084,Human_RBP_ID_27591280,Human_RBP_ID_27799423 Human_Splice_Rec_205866,Human_Splice_Rec_205908,Human_Splice_Rec_205934 GWAS_ID_12778,GWAS_ID_12779,GWAS_ID_12780,GWAS_ID_12781,GWAS_ID_12782,GWAS_ID_12783,GWAS_ID_12784 RMVar_hsa_circ_141087,RMVar_hsa_circ_95280,RMVar_hsa_circ_365720,RMVar_hsa_circ_51137,RMVar_hsa_circ_37847,RMVar_hsa_circ_4424,RMVar_hsa_circ_141088,RMVar_hsa_circ_365825,RMVar_hsa_circ_68461,RMVar_hsa_circ_312008 97139 RMVar_ID_97139 Human_SNP_ID_55961829 m1A Human chr1 - 241923426 241923426 241923426 CCTGCTAGCTACCTTCTTCCAGGAAGATCCTTAAAACCTTTGTCTTCTGTCACTCGCTCTTCCTC CCTGCTAGCTACCTTCTTCCAGGAAGATCCTTCAAACCTTTGTCTTCTGTCACTCGCTCTTCCTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:241923375..241923459 26863196 MeRIP-seq:(Medium) rs1166642714 Functional Loss SNV dbSNP153 33..33 33 - - - 97140 RMVar_ID_97140 Human_SNP_ID_56226551 m1A Human chr1 - 242975219 242975195 242975220 CAAGTTGGGTCTCAGAGGTGATCGGCGATCAGAGGGCGATGAAGGTCTAGATCCATTGAGACAAG CAAGTTGGGTCTCAGAGGTGATCGGCGATCA_________________________TGAGACAAG AATGGATCTAGACCTTCATCGCCCTC A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:242975099..242975226 26863196 MeRIP-seq:(Medium) rs1558287870 Functional Loss DEL dbSNP153 32..56 33 - - - 97141 RMVar_ID_97141 Human_SNP_ID_56293148 m1A Human chr1 + 243254422 243254421 243254423 AGGAAGCCACTCTCTCCTCCCCCGGGTTTACTACAGAGCCAGAGCCTCCACGGGGTGCAGTCGCC AGGAAGCCACTCTCTCCTCCCCCGGGTTTACT__AGAGCCAGAGCCTCCACGGGGTGCAGTCGCC TAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:243254400..243254526 26863196 MeRIP-seq:(Medium) rs1478301552 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_141135 97142 RMVar_ID_97142 Human_SNP_ID_56293171 m1A Human chr1 + 243254527 243254525 243254528 CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCAACCGCCTCACACCCCAAAACCAATCACACAAA CGCGTCCAAAAGGTTGCTCGCCTGACCTCGC___CCGCCTCACACCCCAAAACCAATCACACAAA CCAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:243254388..243254533 26863196 MeRIP-seq:(Medium) rs200248716 Functional Loss DEL dbSNP153 32..34 33 - - - GWAS_ID_12785,GWAS_ID_12786,GWAS_ID_12787,GWAS_ID_12788,GWAS_ID_12789,GWAS_ID_12790,GWAS_ID_12791,GWAS_ID_12792,GWAS_ID_12793,GWAS_ID_12794,GWAS_ID_12795,GWAS_ID_12796,GWAS_ID_12797,GWAS_ID_12798,GWAS_ID_12799,GWAS_ID_12800,GWAS_ID_12801,GWAS_ID_12802,GWAS_ID_12803,GWAS_ID_12804,GWAS_ID_12805,GWAS_ID_12806,GWAS_ID_12807,GWAS_ID_12808,GWAS_ID_12809,GWAS_ID_12810,GWAS_ID_12811,GWAS_ID_12812,GWAS_ID_12813,GWAS_ID_12814,GWAS_ID_12815,GWAS_ID_12816,GWAS_ID_12817,GWAS_ID_12818,GWAS_ID_12819,GWAS_ID_12820,GWAS_ID_12821,GWAS_ID_12822,GWAS_ID_12823,GWAS_ID_12824,GWAS_ID_12825,GWAS_ID_12826,GWAS_ID_12827,GWAS_ID_12828,GWAS_ID_12829,GWAS_ID_12830,GWAS_ID_12831,GWAS_ID_12832,GWAS_ID_12833,GWAS_ID_12834,GWAS_ID_12835,GWAS_ID_12836,GWAS_ID_12837,GWAS_ID_12838,GWAS_ID_12839,GWAS_ID_12840,GWAS_ID_12841,GWAS_ID_12842,GWAS_ID_12843,GWAS_ID_12844,GWAS_ID_12845,GWAS_ID_12846,GWAS_ID_12847,GWAS_ID_12848,GWAS_ID_12849,GWAS_ID_12850,GWAS_ID_12851,GWAS_ID_12852,GWAS_ID_12853,GWAS_ID_12854,GWAS_ID_12855,GWAS_ID_12856,GWAS_ID_12857,GWAS_ID_12858,GWAS_ID_12859,GWAS_ID_12860,GWAS_ID_12861,GWAS_ID_12862,GWAS_ID_12863,GWAS_ID_12864,GWAS_ID_12865,GWAS_ID_12866,GWAS_ID_12867,GWAS_ID_12868 RMVar_hsa_circ_141135 97143 RMVar_ID_97143 Human_SNP_ID_56293173 m1A Human chr1 + 243254527 243254526 243254527 CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCAACCGCCTCACACCCCAAAACCAATCACACAAA CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCC_ACCGCCTCACACCCCAAAACCAATCACACAAA CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:243254388..243254533 26863196 MeRIP-seq:(Medium) rs34428775 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_141135 97144 RMVar_ID_97144 Human_SNP_ID_56293176 m1A Human chr1 + 243254527 243254527 243254527 CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCAACCGCCTCACACCCCAAAACCAATCACACAAA CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCTACCGCCTCACACCCCAAAACCAATCACACAAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:243254388..243254533 26863196 MeRIP-seq:(Medium) rs983662343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141135 97145 RMVar_ID_97145 Human_SNP_ID_56293432 m1A Human chr1 - 243255152 243255150 243255153 GGCCCCGGAGCTCGACCGCAGCGGCAGCGACGACAACAGCGGCGACGACGACGACGACGAGGTGG GGCCCCGGAGCTCGACCGCAGCGGCAGCGAC___AACAGCGGCGACGACGACGACGACGAGGTGG TGTC T CEP170 Ensembl:ENSG00000143702 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:243255101..243255226 26863196 MeRIP-seq:(Medium) rs1225707578 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_743324,Human_RBP_ID_3937569,Human_RBP_ID_4077231,Human_RBP_ID_9319489,Human_RBP_ID_22025734 RMVar_hsa_circ_84463,RMVar_hsa_circ_141132,RMVar_hsa_circ_113576,RMVar_hsa_circ_141136 97146 RMVar_ID_97146 Human_SNP_ID_56293758 m1A Human chr1 + 243256130 243256130 243256130 AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGACATTTCCCCACGTAACTCCCAGCTCTGGGCCT AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGCCATTTCCCCACGTAACTCCCAGCTCTGGGCCT A C SDCCAG8 Ensembl:ENSG00000054282 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:243256079..243256179 26863196 MeRIP-seq:(Medium) rs376221876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4037707,Human_RBP_ID_9360000 97147 RMVar_ID_97147 Human_SNP_ID_56293759 m1A Human chr1 + 243256130 243256130 243256130 AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGACATTTCCCCACGTAACTCCCAGCTCTGGGCCT AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGGCATTTCCCCACGTAACTCCCAGCTCTGGGCCT A G SDCCAG8 Ensembl:ENSG00000054282 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:243256079..243256179 26863196 MeRIP-seq:(Medium) rs376221876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4037707,Human_RBP_ID_9360000 97148 RMVar_ID_97148 Human_SNP_ID_56293760 m1A Human chr1 + 243256130 243256130 243256130 AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGACATTTCCCCACGTAACTCCCAGCTCTGGGCCT AGGCCTGTTGTTCTCGGAAGGGAGAAAGCTGGTCATTTCCCCACGTAACTCCCAGCTCTGGGCCT A T SDCCAG8 Ensembl:ENSG00000054282 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:243256079..243256179 26863196 MeRIP-seq:(Medium) rs376221876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4037707,Human_RBP_ID_9360000 97149 RMVar_ID_97149 Human_SNP_ID_56330496 m1A Human chr1 + 243415770 243415770 243415770 GGAAGCAAAGGCCCAAGCCCTTCAGGCCCAGCAAAGAGAGCAGGAGCTGACACAGAAGATACAGC GGAAGCAAAGGCCCAAGCCCTTCAGGCCCAGCGAAGAGAGCAGGAGCTGACACAGAAGATACAGC A G SDCCAG8 Ensembl:ENSG00000054282 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:243415686..243415772 26863196 MeRIP-seq:(Medium) rs765140932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2136325 Human_Splice_Rec_206498,Human_Splice_Rec_206499,Human_Splice_Rec_206560 RMVar_hsa_circ_278079,RMVar_hsa_circ_273883,RMVar_hsa_circ_60768,RMVar_hsa_circ_274446,RMVar_hsa_circ_323106,RMVar_hsa_circ_71662,RMVar_hsa_circ_141157,RMVar_hsa_circ_301879,RMVar_hsa_circ_141168,RMVar_hsa_circ_16761,RMVar_hsa_circ_323706,RMVar_hsa_circ_353281,RMVar_hsa_circ_50775,RMVar_hsa_circ_35231,RMVar_hsa_circ_141166,RMVar_hsa_circ_141165,RMVar_hsa_circ_351611,RMVar_hsa_circ_377039,RMVar_hsa_circ_356470,RMVar_hsa_circ_141170,RMVar_hsa_circ_286232,RMVar_hsa_circ_355209,RMVar_hsa_circ_141169 97150 RMVar_ID_97150 Human_SNP_ID_56438363 m1A Human chr1 + 243850295 243850295 243850295 CCGGCCGGGCCGGGCCGCGGAGCTGGAGCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGGAGGGG CCGGCCGGGCCGGGCCGCGGAGCTGGAGCGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGGGG A C lnc-ZBTB18-10 RNACentral:URS0000D59790 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:243850222..243850314 26863410 MeRIP-seq:(Medium) rs1300897824 Functional Loss SNV dbSNP153 33..33 33 - - - 97151 RMVar_ID_97151 Human_SNP_ID_56438611 m1A Human chr1 - 243850768 243850745 243850769 ATGTTCTCGCGAGAGGAGAGGGGGCGCGGGGCACCGCTGGTTTGGGGGCGCGGGGAAGCCTGAGG ATGTTCTCGCGAGAGGAGAGGGGGCGCGGGG________________________AAGCCTGAGG TCCCCGCGCCCCCAAACCAGCGGTG T AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:243850595..243850992 26863196 MeRIP-seq:(Medium) rs1407322952 Functional Loss DEL dbSNP153 32..55 33 - - - 97152 RMVar_ID_97152 Human_SNP_ID_56486904 m1A Human chr1 - 244048616 244048615 244048616 GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGGAGGGGGAGGGGAGGGGGCGGGAGGACGCACCAC GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGG_GGGGGAGGGGAGGGGGCGGGAGGACGCACCAC CT C lnc-AKT3-2 RNACentral:URS00008C2559 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244048524..244048734 26863196 MeRIP-seq:(Medium) rs1235975824 Functional Loss DEL dbSNP153 33..33 33 - - - 97153 RMVar_ID_97153 Human_SNP_ID_56486907 m1A Human chr1 - 244048616 244048616 244048616 GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGGAGGGGGAGGGGAGGGGGCGGGAGGACGCACCAC GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGGGGGGGGAGGGGAGGGGGCGGGAGGACGCACCAC T C lnc-AKT3-2 RNACentral:URS00008C2559 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244048524..244048734 26863196 MeRIP-seq:(Medium) rs987635729 Functional Loss SNV dbSNP153 33..33 33 - - - 97154 RMVar_ID_97154 Human_SNP_ID_56486908 m1A Human chr1 - 244048616 244048616 244048616 GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGGAGGGGGAGGGGAGGGGGCGGGAGGACGCACCAC GGGCGGGGGCGGGGGGGGGGCGGGCGCGGGGGCGGGGGAGGGGAGGGGGCGGGAGGACGCACCAC T G lnc-AKT3-2 RNACentral:URS00008C2559 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244048524..244048734 26863196 MeRIP-seq:(Medium) rs987635729 Functional Loss SNV dbSNP153 33..33 33 - - - 97155 RMVar_ID_97155 Human_SNP_ID_56486963 m1A Human chr1 + 244048653 244048651 244048653 CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCACCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCC__CCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244048520..244048740;chr1:244048600..244048668;chr1:244048607..244048764;chr1:244048602..244048691 26863196 MeRIP-seq:(Medium) rs1558146769 Functional Loss DEL dbSNP153 32..33 33 - - - 97156 RMVar_ID_97156 Human_SNP_ID_56486964 m1A Human chr1 + 244048653 244048652 244048653 CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCACCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCC_CCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CA C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244048520..244048740;chr1:244048600..244048668;chr1:244048607..244048764;chr1:244048602..244048691 26863196 MeRIP-seq:(Medium) rs200195758 Functional Loss DEL dbSNP153 33..33 33 - - - 97157 RMVar_ID_97157 Human_SNP_ID_56486968 m1A Human chr1 + 244048653 244048653 244048653 CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCACCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCCCCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244048520..244048740;chr1:244048600..244048668;chr1:244048607..244048764;chr1:244048602..244048691 26863196 MeRIP-seq:(Medium) rs1455538517 Functional Loss SNV dbSNP153 33..33 33 - - - 97158 RMVar_ID_97158 Human_SNP_ID_56486969 m1A Human chr1 + 244048653 244048653 244048653 CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCACCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG CGCGCCCGCCCCCCCCCCGCCCCCGCCCCCCCTCCCGGCCCGGCGGCTCCGCGCTCGCTCCCTCG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244048520..244048740;chr1:244048600..244048668;chr1:244048607..244048764;chr1:244048602..244048691 26863196 MeRIP-seq:(Medium) rs1455538517 Functional Loss SNV dbSNP153 33..33 33 - - - 97159 RMVar_ID_97159 Human_SNP_ID_56487124 m1A Human chr1 - 244048975 244048958 244048975 GCGCCGGGACTCACACGGAGCGGCCCTAAGTCACCGCGTCCCCGCCGCCGCCGCGTCCTCCGCCT GCGCCGGGACTCACACGGAGCGGCCCTAAGTC_________________GCCGCGTCCTCCGCCT CGGCGGCGGGGACGCGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr1:244048593..244049379;chr1:244048708..244048987 26863196 MeRIP-seq:(Medium) rs1357819800 Functional Loss DEL dbSNP153 33..49 33 - - - 97160 RMVar_ID_97160 Human_SNP_ID_56487200 m1A Human chr1 - 244049151 244049148 244049152 CCCCCCGCCGCCCCAACAGCTCCAACCACACAAACTAACTCCACTCGCGGGGGCGCCCCCGACCC CCCCCCGCCGCCCCAACAGCTCCAACCACAC____TAACTCCACTCGCGGGGGCGCCCCCGACCC AGTTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:244049144..244049216 26863196 MeRIP-seq:(Medium) rs1045817898 Functional Loss DEL dbSNP153 32..35 33 - - - 97161 RMVar_ID_97161 Human_SNP_ID_56487385 m1A Human chr1 - 244049619 244049617 244049620 GTGCAGCAGGAAAACACCTTAAACAACAGAGGAGAAAACAGACCCGGGTCACGGCAACAACAAAA GTGCAGCAGGAAAACACCTTAAACAACAGAG___AAAACAGACCCGGGTCACGGCAACAACAAAA TCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:244049604..244049748 26863196 MeRIP-seq:(Medium) rs1157044222 Functional Loss DEL dbSNP153 32..34 33 - - - 97162 RMVar_ID_97162 Human_SNP_ID_56488558 m1A Human chr1 + 244054412 244054412 244054412 CATCCCCCAGGCTGGCGGAGAGGCAGAGCCACACGCCACAGCAGCTGGAAAAACAGTAGCCAGCC CATCCCCCAGGCTGGCGGAGAGGCAGAGCCACGCGCCACAGCAGCTGGAAAAACAGTAGCCAGCC A G ZBTB18 Ensembl:ENSG00000179456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:244054361..244054461 32194978 MeRIP-seq:(Medium) rs529044378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86688,RMVar_hsa_circ_89157,RMVar_hsa_circ_141227,RMVar_hsa_circ_141228 97163 RMVar_ID_97163 Human_SNP_ID_56488559 m1A Human chr1 + 244054412 244054412 244054412 CATCCCCCAGGCTGGCGGAGAGGCAGAGCCACACGCCACAGCAGCTGGAAAAACAGTAGCCAGCC CATCCCCCAGGCTGGCGGAGAGGCAGAGCCACTCGCCACAGCAGCTGGAAAAACAGTAGCCAGCC A T ZBTB18 Ensembl:ENSG00000179456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:244054361..244054461 32194978 MeRIP-seq:(Medium) rs529044378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86688,RMVar_hsa_circ_89157,RMVar_hsa_circ_141227,RMVar_hsa_circ_141228 97164 RMVar_ID_97164 Human_SNP_ID_56488671 m1A Human chr1 + 244054781 244054781 244054781 CCTGAGGGAGGACTCGGTCTTGAGGGAGCTGGACCGGGAGGACAAAGCCAGTGATGATGAGATGA CCTGAGGGAGGACTCGGTCTTGAGGGAGCTGGTCCGGGAGGACAAAGCCAGTGATGATGAGATGA A T ZBTB18 Ensembl:ENSG00000179456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:244054657..244055153 32194978 MeRIP-seq:(Medium) rs1056529186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1743040,Human_RBP_ID_5795220,Human_RBP_ID_8747009,Human_RBP_ID_10878243,Human_RBP_ID_17677264,Human_RBP_ID_17745957 Human_miRNA_ID_2254015 RMVar_hsa_circ_86688,RMVar_hsa_circ_89157,RMVar_hsa_circ_141227,RMVar_hsa_circ_141229,RMVar_hsa_circ_141228 97165 RMVar_ID_97165 Human_SNP_ID_56587830 m1A Human chr1 - 244435506 244435503 244435507 AGGAGGAAGAGAAGGAGGAGGAAGAGGAAACAAACTTCGTTTCATGCACAAAATTATTTAAAATA AGGAGGAAGAGAAGGAGGAGGAAGAGGAAAC____TTCGTTTCATGCACAAAATTATTTAAAATA AGTTT A ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:244435493..244435645 26863196 MeRIP-seq:(Medium) rs1417683891 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_9508143,Human_RBP_ID_17066495,Human_RBP_ID_24541390,Human_RBP_ID_24762398,Human_RBP_ID_26315627 RMVar_hsa_circ_99366,RMVar_hsa_circ_141243,RMVar_hsa_circ_141233,RMVar_hsa_circ_141241,RMVar_hsa_circ_354455,RMVar_hsa_circ_359608,RMVar_hsa_circ_75066,RMVar_hsa_circ_288328,RMVar_hsa_circ_63033,RMVar_hsa_circ_324845,RMVar_hsa_circ_321821 97166 RMVar_ID_97166 Human_SNP_ID_56587834 m1A Human chr1 - 244435523 244435511 244435524 GTAGAGGAGGAGGATGAAGGAGGAAGAGAAGGAGGAGGAAGAGGAAACAAACTTCGTTTCATGCA GTAGAGGAGGAGGATGAAGGAGGAAGAGAAG_____________AAACAAACTTCGTTTCATGCA TCCTCTTCCTCCTC T ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:244435500..244435667 26863196 MeRIP-seq:(Medium) rs1169089846 Functional Loss DEL dbSNP153 32..44 33 - - - Human_RBP_ID_17066495,Human_RBP_ID_24541390,Human_RBP_ID_26315627 RMVar_hsa_circ_99366,RMVar_hsa_circ_141243,RMVar_hsa_circ_141233,RMVar_hsa_circ_141241,RMVar_hsa_circ_354455,RMVar_hsa_circ_359608,RMVar_hsa_circ_75066,RMVar_hsa_circ_288328,RMVar_hsa_circ_63033,RMVar_hsa_circ_324845,RMVar_hsa_circ_321821 97167 RMVar_ID_97167 Human_SNP_ID_56591859 m1A Human chr1 + 244451729 244451729 244451729 CGTCGCCCCACTGCGCACCGAGCACCACCGTCACCCGGTTTCCTCCGGGCCGCGCCCTGGGGCGG CGTCGCCCCACTGCGCACCGAGCACCACCGTCGCCCGGTTTCCTCCGGGCCGCGCCCTGGGGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:244451681..244451922 26863196 MeRIP-seq:(Medium) rs1269577074 Functional Loss SNV dbSNP153 33..33 33 - - - 97168 RMVar_ID_97168 Human_SNP_ID_56591913 m1A Human chr1 - 244451826 244451826 244451826 CGGCCGCCTCTCCTTCGGGCTCTCCTCGCGTCACTGGAGCCATGGCGTTCGCCGAGACCTACCCG CGGCCGCCTCTCCTTCGGGCTCTCCTCGCGTCCCTGGAGCCATGGCGTTCGCCGAGACCTACCCG T G ADSS2 Ensembl:ENSG00000035687 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:244451724..244451886 26863410 MeRIP-seq:(Medium) rs1558285948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223492,Human_RBP_ID_348868,Human_RBP_ID_4038219,Human_RBP_ID_5458573,Human_RBP_ID_5485863,Human_RBP_ID_8755463,Human_RBP_ID_9319493,Human_RBP_ID_9360005,Human_RBP_ID_18415735,Human_RBP_ID_26859107 97169 RMVar_ID_97169 Human_SNP_ID_56638112 m1A Human chr1 + 244645506 244645506 244645506 AGGTGTTGAGCTCTGCAACCTCCACCCCTCCCACCCGCCTCTGGGCACGCAGAGATGGCCCACTG AGGTGTTGAGCTCTGCAACCTCCACCCCTCCCCCCCGCCTCTGGGCACGCAGAGATGGCCCACTG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:244645476..244645525 26863196 MeRIP-seq:(Medium) rs925299583 Functional Loss SNV dbSNP153 33..33 33 - - - 97170 RMVar_ID_97170 Human_SNP_ID_56687743 m1A Human chr1 + 244835715 244835715 244835715 TGCAGGGCGGGTGGAGTCGCGGAGTAGTCCTCATGGCCGCCCCGCCGGAGCCCGGTGAGCCCGAG TGCAGGGCGGGTGGAGTCGCGGAGTAGTCCTCGTGGCCGCCCCGCCGGAGCCCGGTGAGCCCGAG A G COX20 Ensembl:ENSG00000203667 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:244835710..244835859 26863196 MeRIP-seq:(Medium) rs1004657777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1254476,Human_RBP_ID_4074894,Human_RBP_ID_5339033,Human_RBP_ID_22427895,Human_RBP_ID_22871666,Human_RBP_ID_23380147 Human_Splice_Rec_207183,Human_Splice_Rec_207191,Human_Splice_Rec_207195,Human_Splice_Rec_207201 97171 RMVar_ID_97171 Human_SNP_ID_56687744 m1A Human chr1 - 244835716 244835716 244835716 CCTCGGGCTCACCGGGCTCCGGCGGGGCGGCCATGAGGACTACTCCGCGACTCCACCCGCCCTGC CCTCGGGCTCACCGGGCTCCGGCGGGGCGGCCTTGAGGACTACTCCGCGACTCCACCCGCCCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244835398..244836497;chr1:244835354..244835837;chr1:244835350..244839772;chr1:244835651..244835810 26863196 MeRIP-seq:(Medium) rs771264340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5796490 97172 RMVar_ID_97172 Human_SNP_ID_56687745 m1A Human chr1 - 244835716 244835716 244835716 CCTCGGGCTCACCGGGCTCCGGCGGGGCGGCCATGAGGACTACTCCGCGACTCCACCCGCCCTGC CCTCGGGCTCACCGGGCTCCGGCGGGGCGGCCGTGAGGACTACTCCGCGACTCCACCCGCCCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:244835398..244836497;chr1:244835354..244835837;chr1:244835350..244839772;chr1:244835651..244835810 26863196 MeRIP-seq:(Medium) rs771264340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5796490 97173 RMVar_ID_97173 Human_SNP_ID_56689664 m1A Human chr1 - 244842234 244842234 244842234 AAACATACCAGCATCCCAAAGTCACCAAGATAAACCCTCCTACTCCAACATCACATGATCTTCTA AAACATACCAGCATCCCAAAGTCACCAAGATACACCCTCCTACTCCAACATCACATGATCTTCTA T G HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:244842176..244842275 26863196 MeRIP-seq:(Medium) rs147700538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2136831,Human_RBP_ID_5796696,Human_RBP_ID_8047980,Human_RBP_ID_8967566,Human_RBP_ID_9508596,Human_RBP_ID_16974865,Human_RBP_ID_17746198,Human_RBP_ID_22783364,Human_RBP_ID_22860111,Human_RBP_ID_24672690,Human_RBP_ID_27591872 97174 RMVar_ID_97174 Human_SNP_ID_56689669 m1A Human chr1 - 244842243 244842243 244842243 ATACTTAGCAAACATACCAGCATCCCAAAGTCACCAAGATAAACCCTCCTACTCCAACATCACAT ATACTTAGCAAACATACCAGCATCCCAAAGTCGCCAAGATAAACCCTCCTACTCCAACATCACAT T C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:244842176..244842250 26863196 MeRIP-seq:(Medium) rs778772412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1347721,Human_RBP_ID_2136831,Human_RBP_ID_9508596,Human_RBP_ID_10882930,Human_RBP_ID_18569423,Human_RBP_ID_22783364,Human_RBP_ID_22860111,Human_RBP_ID_24672690 97175 RMVar_ID_97175 Human_SNP_ID_56692653 m1A Human chr1 - 244852482 244852482 244852482 TTACTAGAGGAACAGTTTCAGGTTTTGATGCTAATCAGTGTTGTGTCCTAAAGTTGTCCTTTGTG TTACTAGAGGAACAGTTTCAGGTTTTGATGCTTATCAGTGTTGTGTCCTAAAGTTGTCCTTTGTG T A HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs144194483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_349128,Human_RBP_ID_2137016,Human_RBP_ID_4038647,Human_RBP_ID_5797079,Human_RBP_ID_9268431,Human_RBP_ID_9508976,Human_RBP_ID_10883575,Human_RBP_ID_17181790,Human_RBP_ID_22860434,Human_RBP_ID_24673199,Human_RBP_ID_26377791,Human_RBP_ID_27591950 Human_miRNA_ID_1121422 RMVar_hsa_circ_69264,RMVar_hsa_circ_328999,RMVar_hsa_circ_344063,RMVar_hsa_circ_368750,RMVar_hsa_circ_71175,RMVar_hsa_circ_70811,RMVar_hsa_circ_71397,RMVar_hsa_circ_19731,RMVar_hsa_circ_141261 97176 RMVar_ID_97176 Human_SNP_ID_56693490 m1A Human chr1 + 244855547 244855547 244855547 GGGTATGGATAGCCGATTCCACCACTTCCTCCACCGCCACCACCTCTCTGTGGCATGTTGCCCCT GGGTATGGATAGCCGATTCCACCACTTCCTCCCCCGCCACCACCTCTCTGTGGCATGTTGCCCCT A C NONHSAG004867.2 RNACentral:URS00009B46E1 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:244855526..244855550;chr1:244855496..244855662 26863196 MeRIP-seq:(Medium) rs114881415 Functional Loss SNV dbSNP153 33..33 33 - - - 97177 RMVar_ID_97177 Human_SNP_ID_56693491 m1A Human chr1 + 244855547 244855547 244855547 GGGTATGGATAGCCGATTCCACCACTTCCTCCACCGCCACCACCTCTCTGTGGCATGTTGCCCCT GGGTATGGATAGCCGATTCCACCACTTCCTCCGCCGCCACCACCTCTCTGTGGCATGTTGCCCCT A G NONHSAG004867.2 RNACentral:URS00009B46E1 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:244855526..244855550;chr1:244855496..244855662 26863196 MeRIP-seq:(Medium) rs114881415 Functional Loss SNV dbSNP153 33..33 33 - - - 97178 RMVar_ID_97178 Human_SNP_ID_56693511 m1A Human chr1 + 244855595 244855595 244855595 TGTGGCATGTTGCCCCTCCTATTATATCCGCCACGATTCCCAGGGGCTAAAAGACAAGAGCTGTT TGTGGCATGTTGCCCCTCCTATTATATCCGCCCCGATTCCCAGGGGCTAAAAGACAAGAGCTGTT A C NONHSAG004867.2 RNACentral:URS00009B46E1 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:244855551..244855625 26863196 MeRIP-seq:(Medium) rs1327337046 Functional Loss SNV dbSNP153 33..33 33 - - - 97179 RMVar_ID_97179 Human_SNP_ID_56693596 m1A Human chr1 + 244855880 244855880 244855880 AAATTATCACTTGTTTCGATCCTGAACTAAATACAGAACACTCAAAATTAACTTGCCTCCTCCTC AAATTATCACTTGTTTCGATCCTGAACTAAATCCAGAACACTCAAAATTAACTTGCCTCCTCCTC A C NONHSAG004867.2 RNACentral:URS00009B46E1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:244855878..244856096 26863196 MeRIP-seq:(Medium) rs750629405 Functional Loss SNV dbSNP153 33..33 33 - - - 97180 RMVar_ID_97180 Human_SNP_ID_56693601 m1A Human chr1 - 244855889 244855889 244855889 GAAATTTCAGAGGAGGAGGCAAGTTAATTTTGAGTGTTCTGTATTTAGTTCAGGATCGAAACAAG GAAATTTCAGAGGAGGAGGCAAGTTAATTTTGCGTGTTCTGTATTTAGTTCAGGATCGAAACAAG T G HNRNPU Ensembl:ENSG00000153187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:244855887..244856106 26863196 MeRIP-seq:(Medium) rs780932517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1743476,Human_RBP_ID_24673390 RMVar_hsa_circ_62625,RMVar_hsa_circ_69264,RMVar_hsa_circ_328999,RMVar_hsa_circ_344063,RMVar_hsa_circ_368750,RMVar_hsa_circ_71175,RMVar_hsa_circ_70811,RMVar_hsa_circ_71397,RMVar_hsa_circ_141261,RMVar_hsa_circ_96210,RMVar_hsa_circ_112249,RMVar_hsa_circ_351017,RMVar_hsa_circ_141267,RMVar_hsa_circ_362888,RMVar_hsa_circ_141265,RMVar_hsa_circ_141266,RMVar_hsa_circ_141264,RMVar_hsa_circ_368772,RMVar_hsa_circ_111606,RMVar_hsa_circ_266122,RMVar_hsa_circ_68419,RMVar_hsa_circ_141269,RMVar_hsa_circ_141270,RMVar_hsa_circ_378837 97181 RMVar_ID_97181 Human_SNP_ID_56693640 m1A Human chr1 - 244856029 244856029 244856029 GGAAGAAAGCAAAAAGGCTCTTCCACCAGAAAAGAAACAGAACACTGGCTCAAAGAAAAGCAATA GGAAGAAAGCAAAAAGGCTCTTCCACCAGAAAGGAAACAGAACACTGGCTCAAAGAAAAGCAATA T C HNRNPU Ensembl:ENSG00000153187 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs910476955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21712,Human_RBP_ID_976899,Human_RBP_ID_1427015,Human_RBP_ID_1743478,Human_RBP_ID_2137126,Human_RBP_ID_3307137,Human_RBP_ID_4092564,Human_RBP_ID_5797248,Human_RBP_ID_8305421,Human_RBP_ID_9357707,Human_RBP_ID_9509089,Human_RBP_ID_10883781,Human_RBP_ID_18569530,Human_RBP_ID_22139518,Human_RBP_ID_22783523,Human_RBP_ID_22860547,Human_RBP_ID_24541392,Human_RBP_ID_24673397,Human_RBP_ID_26859359 Human_miRNA_ID_2174318,Human_miRNA_ID_2177762 RMVar_hsa_circ_62625,RMVar_hsa_circ_69264,RMVar_hsa_circ_328999,RMVar_hsa_circ_344063,RMVar_hsa_circ_368750,RMVar_hsa_circ_71175,RMVar_hsa_circ_70811,RMVar_hsa_circ_71397,RMVar_hsa_circ_141261,RMVar_hsa_circ_96210,RMVar_hsa_circ_112249,RMVar_hsa_circ_351017,RMVar_hsa_circ_141267,RMVar_hsa_circ_362888,RMVar_hsa_circ_141265,RMVar_hsa_circ_141266,RMVar_hsa_circ_141264,RMVar_hsa_circ_368772,RMVar_hsa_circ_111606,RMVar_hsa_circ_266122,RMVar_hsa_circ_68419,RMVar_hsa_circ_68542,RMVar_hsa_circ_266514 97182 RMVar_ID_97182 Human_SNP_ID_56694166 m1A Human chr1 - 244857711 244857711 244857711 AATGACATTTCTTTTCTTTTCACTAGGTTGTGATGATGATTGGCTTGCCAGGAGCTGGAAAAACT AATGACATTTCTTTTCTTTTCACTAGGTTGTGGTGATGATTGGCTTGCCAGGAGCTGGAAAAACT T C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:244857660..244857761 32194978 MeRIP-seq:(Medium) rs750921542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189903,Human_RBP_ID_1427041,Human_RBP_ID_3934707,Human_RBP_ID_4038761,Human_RBP_ID_5519416,Human_RBP_ID_5797282,Human_RBP_ID_8228464,Human_RBP_ID_8747213,Human_RBP_ID_9357720,Human_RBP_ID_10883862,Human_RBP_ID_18569557,Human_RBP_ID_18966565,Human_RBP_ID_22026599,Human_RBP_ID_22430115,Human_RBP_ID_23380367,Human_RBP_ID_24541395,Human_RBP_ID_24673461,Human_RBP_ID_26309903,Human_RBP_ID_27799457 Human_Splice_Rec_207234,Human_Splice_Rec_207254,Human_Splice_Rec_207286,Human_Splice_Rec_207324,Human_Splice_Rec_207346,Human_Splice_Rec_207366,Human_Splice_Rec_207382,Human_Splice_Rec_207398,Human_Splice_Rec_207418,Human_Splice_Rec_207436,Human_Splice_Rec_207450,Human_Splice_Rec_207468,Human_Splice_Rec_207490,Human_Splice_Rec_207500,Human_Splice_Rec_207522,Human_Splice_Rec_207538,Human_Splice_Rec_207558,Human_Splice_Rec_207574,Human_Splice_Rec_207588,Human_Splice_Rec_207598 RMVar_hsa_circ_62625,RMVar_hsa_circ_69264,RMVar_hsa_circ_368750,RMVar_hsa_circ_71175,RMVar_hsa_circ_70811,RMVar_hsa_circ_71397,RMVar_hsa_circ_141261,RMVar_hsa_circ_112249,RMVar_hsa_circ_351017,RMVar_hsa_circ_53867,RMVar_hsa_circ_362888,RMVar_hsa_circ_141265,RMVar_hsa_circ_141264,RMVar_hsa_circ_266122,RMVar_hsa_circ_68419,RMVar_hsa_circ_68542,RMVar_hsa_circ_266514,RMVar_hsa_circ_374271,RMVar_hsa_circ_75697,RMVar_hsa_circ_55101,RMVar_hsa_circ_75057,RMVar_hsa_circ_141271,RMVar_hsa_circ_141272,RMVar_hsa_circ_267436,RMVar_hsa_circ_307717,RMVar_hsa_circ_363146,RMVar_hsa_circ_71617,RMVar_hsa_circ_141273 97183 RMVar_ID_97183 Human_SNP_ID_56694722 m1A Human chr1 - 244859362 244859362 244859362 TTTAATGATTTGACTTTCAGGTTACAGAGAAGATCCCAGTAAGGCATTTATATACAAAAGATATT TTTAATGATTTGACTTTCAGGTTACAGAGAAGGTCCCAGTAAGGCATTTATATACAAAAGATATT T C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1377845040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21723,Human_RBP_ID_272645,Human_RBP_ID_349227,Human_RBP_ID_856006,Human_RBP_ID_976914,Human_RBP_ID_1743508,Human_RBP_ID_2182726,Human_RBP_ID_5797320,Human_RBP_ID_8747229,Human_RBP_ID_11205079,Human_RBP_ID_19040560,Human_RBP_ID_22635207,Human_RBP_ID_23380384,Human_RBP_ID_24541571,Human_RBP_ID_24556138,Human_RBP_ID_24673528,Human_RBP_ID_26312995,Human_RBP_ID_27592017,Human_RBP_ID_27799473 Human_Splice_Rec_207228,Human_Splice_Rec_207229,Human_Splice_Rec_207248,Human_Splice_Rec_207249,Human_Splice_Rec_207280,Human_Splice_Rec_207281,Human_Splice_Rec_207318,Human_Splice_Rec_207319,Human_Splice_Rec_207340,Human_Splice_Rec_207341,Human_Splice_Rec_207360,Human_Splice_Rec_207361,Human_Splice_Rec_207376,Human_Splice_Rec_207377,Human_Splice_Rec_207392,Human_Splice_Rec_207393,Human_Splice_Rec_207412,Human_Splice_Rec_207413,Human_Splice_Rec_207430,Human_Splice_Rec_207431,Human_Splice_Rec_207445,Human_Splice_Rec_207462,Human_Splice_Rec_207463,Human_Splice_Rec_207484,Human_Splice_Rec_207485,Human_Splice_Rec_207516,Human_Splice_Rec_207517,Human_Splice_Rec_207532,Human_Splice_Rec_207533,Human_Splice_Rec_207553,Human_Splice_Rec_207568,Human_Splice_Rec_207569,Human_Splice_Rec_207583,Human_Splice_Rec_207593,Human_Splice_Rec_207602,Human_Splice_Rec_207603,Human_Splice_Rec_207608,Human_Splice_Rec_207609,Human_Splice_Rec_207616,Human_Splice_Rec_207617 Human_miRNA_ID_2869220,Human_miRNA_ID_3115849 RMVar_hsa_circ_17585,RMVar_hsa_circ_62625,RMVar_hsa_circ_368750,RMVar_hsa_circ_71397,RMVar_hsa_circ_141261,RMVar_hsa_circ_351017,RMVar_hsa_circ_53867,RMVar_hsa_circ_141264,RMVar_hsa_circ_266122,RMVar_hsa_circ_68419,RMVar_hsa_circ_68542,RMVar_hsa_circ_266514,RMVar_hsa_circ_374271,RMVar_hsa_circ_55101,RMVar_hsa_circ_75057,RMVar_hsa_circ_141272,RMVar_hsa_circ_267436,RMVar_hsa_circ_307717,RMVar_hsa_circ_363146,RMVar_hsa_circ_69841,RMVar_hsa_circ_372110,RMVar_hsa_circ_141273,RMVar_hsa_circ_141274,RMVar_hsa_circ_371678,RMVar_hsa_circ_141275 97184 RMVar_ID_97184 Human_SNP_ID_56695034 m1A Human chr1 + 244860344 244860344 244860344 ACAAATCATAAAATTGCATTTACCTTCATCTCAAAACACACTTTGCCTTTTGACACACCATAGGA ACAAATCATAAAATTGCATTTACCTTCATCTCTAAACACACTTTGCCTTTTGACACACCATAGGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:244860326..244860400 26863196 MeRIP-seq:(Medium) rs1180764471 Functional Loss SNV dbSNP153 33..33 33 - - - 97185 RMVar_ID_97185 Human_SNP_ID_56695849 m1A Human chr1 - 244862715 244862714 244862716 GCTCGTGTGTGTTTTAGGGGACGGCAAAACAGAACAGAAAGGCGGAGATAAAAAGAGGGGTGTTA GCTCGTGTGTGTTTTAGGGGACGGCAAAACA__ACAGAAAGGCGGAGATAAAAAGAGGGGTGTTA TTC T HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:244862704..244862788 26863410 MeRIP-seq:(Medium) rs770849021 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_745159,Human_RBP_ID_4038806,Human_RBP_ID_5537587,Human_RBP_ID_10884133,Human_RBP_ID_17102550,Human_RBP_ID_22871669,Human_RBP_ID_23380421,Human_RBP_ID_24673718,Human_RBP_ID_26313008,Human_RBP_ID_26859435 Human_Splice_Rec_207222,Human_Splice_Rec_207223,Human_Splice_Rec_207274,Human_Splice_Rec_207275,Human_Splice_Rec_207312,Human_Splice_Rec_207313,Human_Splice_Rec_207334,Human_Splice_Rec_207335,Human_Splice_Rec_207355,Human_Splice_Rec_207408,Human_Splice_Rec_207409,Human_Splice_Rec_207478,Human_Splice_Rec_207479,Human_Splice_Rec_207512,Human_Splice_Rec_207513,Human_Splice_Rec_207548,Human_Splice_Rec_207549 RMVar_hsa_circ_71397,RMVar_hsa_circ_351017,RMVar_hsa_circ_53867,RMVar_hsa_circ_141264,RMVar_hsa_circ_68419,RMVar_hsa_circ_266514,RMVar_hsa_circ_55101,RMVar_hsa_circ_267436,RMVar_hsa_circ_48637,RMVar_hsa_circ_141276,RMVar_hsa_circ_295098 97186 RMVar_ID_97186 Human_SNP_ID_56695853 m1A Human chr1 - 244862732 244862732 244862732 GGCTTGGCCTTTATGGGGCTCGTGTGTGTTTTAGGGGACGGCAAAACAGAACAGAAAGGCGGAGA GGCTTGGCCTTTATGGGGCTCGTGTGTGTTTTTGGGGACGGCAAAACAGAACAGAAAGGCGGAGA T A HNRNPU Ensembl:ENSG00000153187 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244862651..244862752 26863196 MeRIP-seq:(Medium) rs1411752390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_349232,Human_RBP_ID_745159,Human_RBP_ID_1347750,Human_RBP_ID_4038810,Human_RBP_ID_5797449,Human_RBP_ID_10884133,Human_RBP_ID_17102550,Human_RBP_ID_22019682,Human_RBP_ID_22139583,Human_RBP_ID_22535742,Human_RBP_ID_22860729,Human_RBP_ID_23380421,Human_RBP_ID_24762836,Human_RBP_ID_26859435,Human_RBP_ID_27592033 97187 RMVar_ID_97187 Human_SNP_ID_56696513 m1A Human chr1 - 244863766 244863766 244863766 GCAACAGCCCCAACAGCAGCGCGGGGCCGCCAAGGAGGCCGCGGGGAAGAGCAGCGGCCCCACCT GCAACAGCCCCAACAGCAGCGCGGGGCCGCCAGGGAGGCCGCGGGGAAGAGCAGCGGCCCCACCT T C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:244863630..244863928 26863410 MeRIP-seq:(Medium) rs747403316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4092616,Human_RBP_ID_8305471,Human_RBP_ID_9357736,Human_RBP_ID_22532006,Human_RBP_ID_22783589 Human_Splice_Rec_207221,Human_Splice_Rec_207273,Human_Splice_Rec_207333,Human_Splice_Rec_207459,Human_Splice_Rec_207477,Human_Splice_Rec_207511,Human_Splice_Rec_207611 97188 RMVar_ID_97188 Human_SNP_ID_56696514 m1A Human chr1 - 244863766 244863766 244863766 GCAACAGCCCCAACAGCAGCGCGGGGCCGCCAAGGAGGCCGCGGGGAAGAGCAGCGGCCCCACCT GCAACAGCCCCAACAGCAGCGCGGGGCCGCCACGGAGGCCGCGGGGAAGAGCAGCGGCCCCACCT T G HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:244863630..244863928 26863410 MeRIP-seq:(Medium) rs747403316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4092616,Human_RBP_ID_8305471,Human_RBP_ID_9357736,Human_RBP_ID_22532006,Human_RBP_ID_22783589 Human_Splice_Rec_207221,Human_Splice_Rec_207273,Human_Splice_Rec_207333,Human_Splice_Rec_207459,Human_Splice_Rec_207477,Human_Splice_Rec_207511,Human_Splice_Rec_207611 97189 RMVar_ID_97189 Human_SNP_ID_56696566 m1A Human chr1 - 244863862 244863862 244863862 CCAGGAAGGGGAAGATGAGCTCGGGGACGAAGAGGAAGGCGCGGGCGACGAGAACGGGCACGGGG CCAGGAAGGGGAAGATGAGCTCGGGGACGAAGGGGAAGGCGCGGGCGACGAGAACGGGCACGGGG T C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr1:244863601..244864525;chr1:244863601..244864144 26863196 MeRIP-seq:(Medium) rs375569535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224238,Human_RBP_ID_3934710,Human_RBP_ID_4038833,Human_RBP_ID_5157908,Human_RBP_ID_5537589,Human_RBP_ID_5797461,Human_RBP_ID_8305472,Human_RBP_ID_8747238,Human_RBP_ID_9253200,Human_RBP_ID_9357737,Human_RBP_ID_9562303,Human_RBP_ID_10884174,Human_RBP_ID_17066502,Human_RBP_ID_17647239,Human_RBP_ID_18569633,Human_RBP_ID_22019691,Human_RBP_ID_22139595,Human_RBP_ID_22430116,Human_RBP_ID_22735197,Human_RBP_ID_22783590,Human_RBP_ID_22860741,Human_RBP_ID_23122400,Human_RBP_ID_24541397,Human_RBP_ID_24762847,Human_RBP_ID_26309915,Human_RBP_ID_26859456,Human_RBP_ID_27799486 97190 RMVar_ID_97190 Human_SNP_ID_56696641 m1A Human chr1 - 244864042 244864024 244864042 CGCGGCCGGCGGCGATGAAGAGGAGGAGGAAGAGGAAGAGGAGGAGGAAGGAATCTCCGCTCTGG CGCGGCCGGCGGCGATGAAGAGGAGGAGGAAG__________________GAATCTCCGCTCTGG CCTTCCTCCTCCTCTTCCT C HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1558190683 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_5537591,Human_RBP_ID_5797468,Human_RBP_ID_9253201,Human_RBP_ID_17763234,Human_RBP_ID_18523093,Human_RBP_ID_22783595,Human_RBP_ID_22871099,Human_RBP_ID_23117586,Human_RBP_ID_24541400,Human_RBP_ID_26315670,Human_RBP_ID_26859459 97191 RMVar_ID_97191 Human_SNP_ID_56696772 m1A Human chr1 + 244864325 244864325 244864325 AGGCGAGGAACTCATGGTGAGGGCCCCGATTCACCGCTAGGCGCTGCCTCAAACTCGGCTCCGCT AGGCGAGGAACTCATGGTGAGGGCCCCGATTCGCCGCTAGGCGCTGCCTCAAACTCGGCTCCGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244864276..244864550 26863196 MeRIP-seq:(Medium) rs777008090 Functional Loss SNV dbSNP153 33..33 33 - - - 97192 RMVar_ID_97192 Human_SNP_ID_56696820 m1A Human chr1 - 244864411 244864411 244864411 TGCAGCACGAACCCATCTCCAGCCGCAGCCGCAGCCGCCGCCCGGGCCGAGGAGCAGCCGCAGCA TGCAGCACGAACCCATCTCCAGCCGCAGCCGCCGCCGCCGCCCGGGCCGAGGAGCAGCCGCAGCA T G HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:244864176..244864525 26863410 MeRIP-seq:(Medium) rs1033668812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25253,Human_RBP_ID_224241,Human_RBP_ID_1743560,Human_RBP_ID_4074898,Human_RBP_ID_5797486,Human_RBP_ID_9357746,Human_RBP_ID_17746350,Human_RBP_ID_18569640,Human_RBP_ID_22532007,Human_RBP_ID_24541403,Human_RBP_ID_26309920,Human_RBP_ID_26859465,Human_RBP_ID_27179600,Human_RBP_ID_27801782 97193 RMVar_ID_97193 Human_SNP_ID_56725402 m1A Human chr1 - 244970445 244970445 244970445 CGAGGGCAGCGGCTCCCCGGCTCCCCTACCTTACCTTCCCTGTCCTTCTCGTCCGCCATCTTGCT CGAGGGCAGCGGCTCCCCGGCTCCCCTACCTTCCCTTCCCTGTCCTTCTCGTCCGCCATCTTGCT T G AL356512.1 Ensembl:ENSG00000272195 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:244969808..244970613;chr1:244970000..244970606 26863196 MeRIP-seq:(Medium) rs753483007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5273032,Human_RBP_ID_19323200 97194 RMVar_ID_97194 Human_SNP_ID_56767343 m1A Human chr1 - 245143155 245143151 245143155 GTGGGTGGACAGACGGGTGGGTGGACAGATGGACGGGTGGACAGGTGGACAGACAGGTGGACAGA GTGGGTGGACAGACGGGTGGGTGGACAGATGG____GTGGACAGGTGGACAGACAGGTGGACAGA CCCGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:245143083..245143185 26863196 MeRIP-seq:(Medium) rs969100939 Functional Loss DEL dbSNP153 33..36 33 - - - 97195 RMVar_ID_97195 Human_SNP_ID_56905911 m1A Human chr1 + 245686001 245686001 245686001 CTCCCAGCCTCCAAGATGCAGAGGAGTCACTCACCTGTGCCCGCCGCGGCACCCGCCCACAGCCC CTCCCAGCCTCCAAGATGCAGAGGAGTCACTCCCCTGTGCCCGCCGCGGCACCCGCCCACAGCCC A C KIF26B Ensembl:ENSG00000162849 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:245685951..245686166 26863196 MeRIP-seq:(Medium) rs559871404 Functional Loss SNV dbSNP153 33..33 33 - - - 97196 RMVar_ID_97196 Human_SNP_ID_56906824 m1A Human chr1 - 245687863 245687863 245687863 GGAGGCCCGCCGGGAAGGCGGCTGGTTGGTTCAGGGGGCTGCTGGTGCCGCTGCCGCTGGCACTG GGAGGCCCGCCGGGAAGGCGGCTGGTTGGTTCGGGGGGCTGCTGGTGCCGCTGCCGCTGGCACTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:245687817..245687911 26863196 MeRIP-seq:(Medium) rs1436456036 Functional Loss SNV dbSNP153 33..33 33 - - - 97197 RMVar_ID_97197 Human_SNP_ID_56935432 m1A Human chr1 + 245798392 245798392 245798392 AAGGATCTTGACCTGTCAACACACACACGCGCACACACACACACACATACACACACATACACACC AAGGATCTTGACCTGTCAACACACACACGCGCGCACACACACACACATACACACACATACACACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:245798390..245798519 26863196 MeRIP-seq:(Medium) rs1558351259 Functional Loss SNV dbSNP153 33..33 33 - - - 97198 RMVar_ID_97198 Human_SNP_ID_56984889 m1A Human chr1 - 245988492 245988492 245988492 CAGAAGCTACAGAAGAAGATGGTTACATTTCAAGTGGGCAGGTGCCGTTTGCTTATGAGCACCAT CAGAAGCTACAGAAGAAGATGGTTACATTTCAGGTGGGCAGGTGCCGTTTGCTTATGAGCACCAT T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:245988452..245988525 26863196 MeRIP-seq:(Medium) rs545110815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_207923,Human_Splice_Rec_207933 RMVar_hsa_circ_141304,RMVar_hsa_circ_82632,RMVar_hsa_circ_141300,RMVar_hsa_circ_102005,RMVar_hsa_circ_316706,RMVar_hsa_circ_121587,RMVar_hsa_circ_106696,RMVar_hsa_circ_141306,RMVar_hsa_circ_141307,RMVar_hsa_circ_141305,RMVar_hsa_circ_141316,RMVar_hsa_circ_295940,RMVar_hsa_circ_358510,RMVar_hsa_circ_374426,RMVar_hsa_circ_123758,RMVar_hsa_circ_80673,RMVar_hsa_circ_141317,RMVar_hsa_circ_267121,RMVar_hsa_circ_141314,RMVar_hsa_circ_141315,RMVar_hsa_circ_267330 97199 RMVar_ID_97199 Human_SNP_ID_56984890 m1A Human chr1 - 245988492 245988492 245988492 CAGAAGCTACAGAAGAAGATGGTTACATTTCAAGTGGGCAGGTGCCGTTTGCTTATGAGCACCAT CAGAAGCTACAGAAGAAGATGGTTACATTTCACGTGGGCAGGTGCCGTTTGCTTATGAGCACCAT T G SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:245988452..245988525 26863196 MeRIP-seq:(Medium) rs545110815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_207923,Human_Splice_Rec_207933 RMVar_hsa_circ_141304,RMVar_hsa_circ_82632,RMVar_hsa_circ_141300,RMVar_hsa_circ_102005,RMVar_hsa_circ_316706,RMVar_hsa_circ_121587,RMVar_hsa_circ_106696,RMVar_hsa_circ_141306,RMVar_hsa_circ_141307,RMVar_hsa_circ_141305,RMVar_hsa_circ_141316,RMVar_hsa_circ_295940,RMVar_hsa_circ_358510,RMVar_hsa_circ_374426,RMVar_hsa_circ_123758,RMVar_hsa_circ_80673,RMVar_hsa_circ_141317,RMVar_hsa_circ_267121,RMVar_hsa_circ_141314,RMVar_hsa_circ_141315,RMVar_hsa_circ_267330 97200 RMVar_ID_97200 Human_SNP_ID_57003838 m1A Human chr1 - 246064036 246064036 246064036 TTTGGCCTAGAAGAGATGAGGGACAGTGAAGAAGTAGGAATTGGGATTATTTCTTGGTTTCTGGC TTTGGCCTAGAAGAGATGAGGGACAGTGAAGAGGTAGGAATTGGGATTATTTCTTGGTTTCTGGC T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246064034..246064169 26863196 MeRIP-seq:(Medium) rs1353241232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141304,RMVar_hsa_circ_82632,RMVar_hsa_circ_141300,RMVar_hsa_circ_102005,RMVar_hsa_circ_316706,RMVar_hsa_circ_121587,RMVar_hsa_circ_106696,RMVar_hsa_circ_141306,RMVar_hsa_circ_141307,RMVar_hsa_circ_141305,RMVar_hsa_circ_141316,RMVar_hsa_circ_295940,RMVar_hsa_circ_358510,RMVar_hsa_circ_374426,RMVar_hsa_circ_123758,RMVar_hsa_circ_80673,RMVar_hsa_circ_141317,RMVar_hsa_circ_267121,RMVar_hsa_circ_141314,RMVar_hsa_circ_141315,RMVar_hsa_circ_267330 97201 RMVar_ID_97201 Human_SNP_ID_57011511 m1A Human chr1 + 246094827 246094827 246094827 TCATAACAAACCTAACACACATCACAGTTCCCACTTTTCATATCTAACCTGCATCTAAATCTGCT TCATAACAAACCTAACACACATCACAGTTCCCGCTTTTCATATCTAACCTGCATCTAAATCTGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246094824..246094968 26863196 MeRIP-seq:(Medium) rs1294179537 Functional Loss SNV dbSNP153 33..33 33 - - - 97202 RMVar_ID_97202 Human_SNP_ID_57015057 m1A Human chr1 + 246108885 246108885 246108885 CACTGCTTTGCACACACTCTTCTCTTTCTCAGAAGGTCCTTTCCCCTCCTCCTGTTGGTGCAGCC CACTGCTTTGCACACACTCTTCTCTTTCTCAGGAGGTCCTTTCCCCTCCTCCTGTTGGTGCAGCC A G AC092801.1 Ensembl:ENSG00000226876 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246108883..246108960 26863196 MeRIP-seq:(Medium) rs1310612575 Functional Loss SNV dbSNP153 33..33 33 - - - 97203 RMVar_ID_97203 Human_SNP_ID_57021837 m1A Human chr1 + 246136316 246136316 246136316 GCTCTCCATTTTTTAGTTGGCTACCCACCCCCAATTCCAAAAGCATAGGTCCATCATGTTCAGAT GCTCTCCATTTTTTAGTTGGCTACCCACCCCCCATTCCAAAAGCATAGGTCCATCATGTTCAGAT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:246136224..246136351 26863196 MeRIP-seq:(Medium) rs1474423461 Functional Loss SNV dbSNP153 33..33 33 - - - 97204 RMVar_ID_97204 Human_SNP_ID_57113465 m1A Human chr1 - 246501461 246501461 246501461 ACATGCTTAGAAGTAGTGTGTGTCTTGATACAACAGGTACGGGGTGTGGCAGAATGTGGCCAAGG ACATGCTTAGAAGTAGTGTGTGTCTTGATACAGCAGGTACGGGGTGTGGCAGAATGTGGCCAAGG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246501458..246501600 26863196 MeRIP-seq:(Medium) rs1386390443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17103975 97205 RMVar_ID_97205 Human_SNP_ID_57114902 m1A Human chr1 + 246507127 246507127 246507127 GCACACCGTGTACGCCAAGGGATCCGAGCGGAAGAGTAGCTCTCCGGGGCGCAGCGGGGTCACGG GCACACCGTGTACGCCAAGGGATCCGAGCGGACGAGTAGCTCTCCGGGGCGCAGCGGGGTCACGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:246507076..246507275 26863196 MeRIP-seq:(Medium) rs1392584196 Functional Loss SNV dbSNP153 33..33 33 - - - 97206 RMVar_ID_97206 Human_SNP_ID_57114928 m1A Human chr1 - 246507173 246507173 246507173 AAGGTGGAAAAGTTCGCAACCGCCAAGAGGGGAAACGGGCTGCGCGCCGTGACCCCGCTGCGCCC AAGGTGGAAAAGTTCGCAACCGCCAAGAGGGGGAACGGGCTGCGCGCCGTGACCCCGCTGCGCCC T C SMYD3 Ensembl:ENSG00000185420 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:246507122..246507253;chr1:246507122..246507244 26863196 MeRIP-seq:(Medium) rs1241540613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4038962,Human_RBP_ID_9360032,Human_RBP_ID_18969778,Human_RBP_ID_26313044 97207 RMVar_ID_97207 Human_SNP_ID_57132268 m1A Human chr1 + 246566856 246566856 246566856 CTCTCAGGTCGCCTGTTTTCCTCTCCTTTCTCAGCTACTGTGGGTCTCCTATTGCTGCGCGTCGC CTCTCAGGTCGCCTGTTTTCCTCTCCTTTCTCGGCTACTGTGGGTCTCCTATTGCTGCGCGTCGC A G CNST Ensembl:ENSG00000162852 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246566847..246566964 26863196 MeRIP-seq:(Medium) rs983732277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8305929,Human_RBP_ID_24399148 RMVar_hsa_circ_119269,RMVar_hsa_circ_141348 97208 RMVar_ID_97208 Human_SNP_ID_57151175 m1A Human chr1 - 246639227 246639227 246639227 TCCAGAAGGCTCTCATCTCAGCCCCCGTTCTCACTCTCCCAGACCTCACCAAACCTTTCTCTCTA TCCAGAAGGCTCTCATCTCAGCCCCCGTTCTCTCTCTCCCAGACCTCACCAAACCTTTCTCTCTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:246639187..246639353 26863196 MeRIP-seq:(Medium) rs1032435890 Functional Loss SNV dbSNP153 33..33 33 - - - 97209 RMVar_ID_97209 Human_SNP_ID_57175151 m1A Human chr1 + 246724520 246724520 246724520 CGTGACCGAGGAGGTGGCCCGGGAGCAGGTGGACCCGGAGCGGAGCTCCCGCCTGCCCTGGGCCG CGTGACCGAGGAGGTGGCCCGGGAGCAGGTGGGCCCGGAGCGGAGCTCCCGCCTGCCCTGGGCCG A G SCCPDH Ensembl:ENSG00000143653 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:246724478..246724625 26863196 MeRIP-seq:(Medium) rs971628158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743322,Human_RBP_ID_4073368,Human_RBP_ID_5312037,Human_RBP_ID_17746508,Human_RBP_ID_22428911 Human_Splice_Rec_208117 RMVar_hsa_circ_109819,RMVar_hsa_circ_141357 97210 RMVar_ID_97210 Human_SNP_ID_57175797 m1A Human chr1 - 246726879 246726878 246726879 AGATGACAGTGTTGGTCTTCCTAAAATAAGAAACAAATGAAGGAAAGTAAATCCCAGTAGAGGAT AGATGACAGTGTTGGTCTTCCTAAAATAAGAA_CAAATGAAGGAAAGTAAATCCCAGTAGAGGAT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:246726876..246726925;chr1:246726876..246726900 26863196 MeRIP-seq:(Medium) rs763379509 Functional Loss DEL dbSNP153 33..33 33 - - - 97211 RMVar_ID_97211 Human_SNP_ID_57191932 m1A Human chr1 - 246790925 246790925 246790925 GCTGTCCCCATGCATCATGGGCCACAGCACACAGGAGGCCCCGAGATGCCACCTGCCATCCTCCG GCTGTCCCCATGCATCATGGGCCACAGCACACCGGAGGCCCCGAGATGCCACCTGCCATCCTCCG T G KIF28P Ensembl:ENSG00000223519 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:246790900..246791079 26863196 MeRIP-seq:(Medium) rs922016024 Functional Loss SNV dbSNP153 33..33 33 - - - 97212 RMVar_ID_97212 Human_SNP_ID_57232444 m1A Human chr1 - 246931271 246931245 246931271 TTCGCGTCCTGCGCCGGCAGTCGGGTCCCTTTACGGACGGCCGGGGCCGCGACCCTTTCCCACTG TTCGCGTCCTGCGCCGGCAGTCGGGTCCCTTT__________________________CCCACTG GAAAGGGTCGCGGCCCCGGCCGTCCGT G AHCTF1 Ensembl:ENSG00000153207 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:246931267..246931410;chr1:246931268..246931496 26863196 MeRIP-seq:(Medium) rs1205150674 Functional Loss DEL dbSNP153 33..58 33 - - - Human_RBP_ID_17101415,Human_RBP_ID_22024469,Human_RBP_ID_26773284 97213 RMVar_ID_97213 Human_SNP_ID_57232749 m1A Human chr1 - 246931888 246931888 246931888 AGCGGGGCCGGCGCTGTCCGAGGCGAGCAGGCAGCGTTGCAAGGGGAAGGACCCAGAAGCGCGGC AGCGGGGCCGGCGCTGTCCGAGGCGAGCAGGCGGCGTTGCAAGGGGAAGGACCCAGAAGCGCGGC T C AHCTF1 Ensembl:ENSG00000153207 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:246931601..246931978;chr1:246931601..246931950 26863196 MeRIP-seq:(Medium) rs970067140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224244,Human_RBP_ID_4076534,Human_RBP_ID_9271914,Human_RBP_ID_17100060,Human_RBP_ID_18415167 RMVar_hsa_circ_90516,RMVar_hsa_circ_141408 97214 RMVar_ID_97214 Human_SNP_ID_57232750 m1A Human chr1 - 246931888 246931888 246931888 AGCGGGGCCGGCGCTGTCCGAGGCGAGCAGGCAGCGTTGCAAGGGGAAGGACCCAGAAGCGCGGC AGCGGGGCCGGCGCTGTCCGAGGCGAGCAGGCCGCGTTGCAAGGGGAAGGACCCAGAAGCGCGGC T G AHCTF1 Ensembl:ENSG00000153207 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr1:246931601..246931978;chr1:246931601..246931950 26863196 MeRIP-seq:(Medium) rs970067140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224244,Human_RBP_ID_4076534,Human_RBP_ID_9271914,Human_RBP_ID_17100060,Human_RBP_ID_18415167 RMVar_hsa_circ_90516,RMVar_hsa_circ_141408 97215 RMVar_ID_97215 Human_SNP_ID_57326436 m1A Human chr1 + 247299307 247299307 247299307 TTAAACAAAGGGAGGTTTGGAGACAGACACGCACACAGCAAGAGTGCCATGTGGAGATGAAGGCA TTAAACAAAGGGAGGTTTGGAGACAGACACGCGCACAGCAAGAGTGCCATGTGGAGATGAAGGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:247299257..247299558 32194978 MeRIP-seq:(Medium) rs1227327281 Functional Loss SNV dbSNP153 33..33 33 - - - 97216 RMVar_ID_97216 Human_SNP_ID_57326711 m1A Human chr1 - 247300448 247300448 247300448 GCCCCCTCACCTTGGTACTGATCAGCGCCCCCACCCAGGACATACCTTCCCCAGGATAGAGAGCA GCCCCCTCACCTTGGTACTGATCAGCGCCCCCCCCCAGGACATACCTTCCCCAGGATAGAGAGCA T G ZNF496 Ensembl:ENSG00000162714 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:247300405..247300506 32194978 MeRIP-seq:(Medium) rs1005743808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27396448 RMVar_hsa_circ_96820,RMVar_hsa_circ_141424,RMVar_hsa_circ_83101,RMVar_hsa_circ_141425 97217 RMVar_ID_97217 Human_SNP_ID_57326811 m1A Human chr1 - 247300706 247300706 247300706 CGGCAAGGCCAAACTGAGCTTCCAGTGCTGTGAGTGTGGGAAGGCCTTCCAGCGGCACGACCACC CGGCAAGGCCAAACTGAGCTTCCAGTGCTGTGGGTGTGGGAAGGCCTTCCAGCGGCACGACCACC T C ZNF496 Ensembl:ENSG00000162714 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:247300655..247301300 32194978 MeRIP-seq:(Medium) rs956110622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18569928,Human_RBP_ID_27396456 RMVar_hsa_circ_96820,RMVar_hsa_circ_141424,RMVar_hsa_circ_83101,RMVar_hsa_circ_141425 97218 RMVar_ID_97218 Human_SNP_ID_57334503 m1A Human chr1 - 247329216 247329216 247329216 GAGCAGGCTGTGGCCGCGGTGGAGGCACTGGAACGGGAGCCCGGGAGACCCTGGCAGTGGGTGAG GAGCAGGCTGTGGCCGCGGTGGAGGCACTGGAGCGGGAGCCCGGGAGACCCTGGCAGTGGGTGAG T C ZNF496 Ensembl:ENSG00000162714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:247328779..247329312 26863196 MeRIP-seq:(Medium) rs749905930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_856030,Human_RBP_ID_5136541,Human_RBP_ID_18969797 Human_Splice_Rec_208727,Human_Splice_Rec_208739,Human_Splice_Rec_208759,Human_Splice_Rec_208767 RMVar_hsa_circ_73657,RMVar_hsa_circ_351460 97219 RMVar_ID_97219 Human_SNP_ID_57335311 m1A Human chr1 - 247331806 247331806 247331806 CCGCGGCGGCCAGGCCTGCGCCGCCCGCCAACAGGGACGCGCCGCGGCGGTGAGTGCACCCCGGC CCGCGGCGGCCAGGCCTGCGCCGCCCGCCAACTGGGACGCGCCGCGGCGGTGAGTGCACCCCGGC T A ZNF496 Ensembl:ENSG00000162714 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:247331768..247331844 26863196 MeRIP-seq:(Medium) rs1319950080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074915 Human_Splice_Rec_208753,Human_Splice_Rec_208761 97220 RMVar_ID_97220 Human_SNP_ID_57335327 m1A Human chr1 + 247331840 247331834 247331840 TTGGCGGGCGGCGCAGGCCTGGCCGCCGCGGGAGCCCGCCGGACGCCGAGGAAAGGAAAGGCCGG TTGGCGGGCGGCGCAGGCCTGGCCGCC______GCCCGCCGGACGCCGAGGAAAGGAAAGGCCGG CGCGGGA C lnc-NLRP3-1 RNACentral:URS00009C11AD lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr1:247331716..247331850;chr1:247331696..247331881 26863196 MeRIP-seq:(Medium) rs951261425 Functional Loss DEL dbSNP153 28..33 33 - - - 97221 RMVar_ID_97221 Human_SNP_ID_57335527 m1A Human chr1 + 247332356 247332356 247332356 CCGGGCCGCCCAGCCCCTCCTGCCGCTGCGGGACGCCGAAGGTAGCGCTCACATCCGCGCCTTCC CCGGGCCGCCCAGCCCCTCCTGCCGCTGCGGGGCGCCGAAGGTAGCGCTCACATCCGCGCCTTCC A G lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3,lnc-NLRP3-1:4,lnc-NLRP3-1:5 RNACentral:URS00008B71DA,RNACentral:URS00008BD04F,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD,RNACentral:URS0000D574FC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:247332310..247332567 26863196 MeRIP-seq:(Medium) rs991716606 Functional Loss SNV dbSNP153 33..33 33 - - - 97222 RMVar_ID_97222 Human_SNP_ID_57335937 m1A Human chr1 + 247334108 247334104 247334109 GGGAGGGGCTGGTAACAGTCATGGTATTAAAGAGGAGGGCAGGCAGGCCTTACTGTGAAGGTGGT GGGAGGGGCTGGTAACAGTCATGGTATTA_____GAGGGCAGGCAGGCCTTACTGTGAAGGTGGT AAAGAG A lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3,lnc-NLRP3-1:4,lnc-NLRP3-1:5 RNACentral:URS00008B71DA,RNACentral:URS00008BD04F,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD,RNACentral:URS0000D574FC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:247334057..247334348 26863196 MeRIP-seq:(Medium) rs572144867 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_2140198 97223 RMVar_ID_97223 Human_SNP_ID_57336234 m1A Human chr1 + 247335336 247335336 247335336 GGAGGGCAGACCCTGCGAAATGCCAGCCCTGGACCGTGGGAGCCCAAGGGGTTAGTGGAGGAGAA GGAGGGCAGACCCTGCGAAATGCCAGCCCTGGCCCGTGGGAGCCCAAGGGGTTAGTGGAGGAGAA A C lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3,lnc-NLRP3-1:4 RNACentral:URS00008B71DA,RNACentral:URS00008BD04F,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:247335287..247335495 26863196 MeRIP-seq:(Medium) rs942422453 Functional Loss SNV dbSNP153 33..33 33 - - - 97224 RMVar_ID_97224 Human_SNP_ID_57471124 m1A Human chr1 + 247876122 247876122 247876122 AGGAGCAGAGTGGGGTTTAGGGGTCTGTCAAGACACACTGCCAAGAAAGGGGGAAACCACGCCAT AGGAGCAGAGTGGGGTTTAGGGGTCTGTCAAGGCACACTGCCAAGAAAGGGGGAAACCACGCCAT A G TRIM58 Ensembl:ENSG00000162722 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:247876071..247876171 32194978 MeRIP-seq:(Medium) rs777083249 Functional Loss SNV dbSNP153 33..33 33 - - - 97225 RMVar_ID_97225 Human_SNP_ID_57717844 m1A Human chr1 + 248811141 248811141 248811141 ACCCACTAGCACCTTGGCAATGTTGAGGACCCAGCCCAGCGGAAACACCATACCCACAGGAGCCA ACCCACTAGCACCTTGGCAATGTTGAGGACCCGGCCCAGCGGAAACACCATACCCACAGGAGCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:248811094..248811245 32194978 MeRIP-seq:(Medium) rs1430916681 Functional Loss SNV dbSNP153 33..33 33 - - - 97226 RMVar_ID_97226 Human_SNP_ID_57717889 m1A Human chr1 + 248811351 248811351 248811351 GTGGTGTCTTCCGGAGGCACACAGTACATCTTACAGGTTACACACGGGCAGGCTGGAGCAGGACG GTGGTGTCTTCCGGAGGCACACAGTACATCTTGCAGGTTACACACGGGCAGGCTGGAGCAGGACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248811301..248811392 26863196 MeRIP-seq:(Medium) rs1158814794 Functional Loss SNV dbSNP153 33..33 33 - - - 97227 RMVar_ID_97227 Human_SNP_ID_57718144 m1A Human chr1 + 248811966 248811966 248811966 CGGGCTCCGCCGTCGCTGCCCCGGCGCCCTCCACTCCGCGTTCCCAGCTCTTGGCCGTCCAGACT CGGGCTCCGCCGTCGCTGCCCCGGCGCCCTCCGCTCCGCGTTCCCAGCTCTTGGCCGTCCAGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:248811915..248811995 26863196 MeRIP-seq:(Medium) rs1288365650 Functional Loss SNV dbSNP153 33..33 33 - - - 97228 RMVar_ID_97228 Human_SNP_ID_57718231 m1A Human chr1 + 248812135 248812135 248812135 CGGGGCCGGGCCCCAGGCTGCTGCCCTCCTCCAGCCCCGCACCCTCGGCCCCCTCAATCCCGCTG CGGGGCCGGGCCCCAGGCTGCTGCCCTCCTCCGGCCCCGCACCCTCGGCCCCCTCAATCCCGCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:248812090..248812240 26863196 MeRIP-seq:(Medium) rs958188509 Functional Loss SNV dbSNP153 33..33 33 - - - 97229 RMVar_ID_97229 Human_SNP_ID_57718414 m1A Human chr1 - 248812578 248812578 248812578 CAGGTCAGGAGCAGGATTGCTGGGGAGGAACAACGCAGAGCAAGTGGAGCAGGGAAGGGTGTTGT CAGGTCAGGAGCAGGATTGCTGGGGAGGAACAGCGCAGAGCAAGTGGAGCAGGGAAGGGTGTTGT T C SH3BP5L Ensembl:ENSG00000175137 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:248812574..248812656 26863196 MeRIP-seq:(Medium) rs187528799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933 97230 RMVar_ID_97230 Human_SNP_ID_57718419 m1A Human chr1 - 248812601 248812601 248812601 GGAAGGCTCTGGAAGGTGGGGCTCAGGTCAGGAGCAGGATTGCTGGGGAGGAACAACGCAGAGCA GGAAGGCTCTGGAAGGTGGGGCTCAGGTCAGGGGCAGGATTGCTGGGGAGGAACAACGCAGAGCA T C SH3BP5L Ensembl:ENSG00000175137 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:248812598..248812760 26863196 MeRIP-seq:(Medium) rs1295706277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933 97231 RMVar_ID_97231 Human_SNP_ID_57718538 m1A Human chr1 + 248813023 248813023 248813023 CCAGGATCTGGCTGAACTGGGCCTTGAGCTCAAAGTAGGGGCGGCTCTTGCCGATGGCCCTCCGG CCAGGATCTGGCTGAACTGGGCCTTGAGCTCAGAGTAGGGGCGGCTCTTGCCGATGGCCCTCCGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:248812292..248813211 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 97232 RMVar_ID_97232 Human_SNP_ID_57718955 m1A Human chr1 - 248814522 248814518 248814522 CAACGCTGCTCGAGAAATGGTGTTTGTGGCTGAGCAGGGCGTCATGGCTGACAAGAACCGACTGG CAACGCTGCTCGAGAAATGGTGTTTGTGGCTG____GGGCGTCATGGCTGACAAGAACCGACTGG CTGCT C SH3BP5L Ensembl:ENSG00000175137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248814159..248814734 26863196 MeRIP-seq:(Medium) rs1553292444 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_744193,Human_RBP_ID_10896253,Human_RBP_ID_26389340,Human_RBP_ID_27799510 Human_Splice_Rec_209286,Human_Splice_Rec_209287,Human_Splice_Rec_209302,Human_Splice_Rec_209303 RMVar_hsa_circ_88240,RMVar_hsa_circ_141434,RMVar_hsa_circ_141435 97233 RMVar_ID_97233 Human_SNP_ID_57718956 m1A Human chr1 - 248814522 248814522 248814522 CAACGCTGCTCGAGAAATGGTGTTTGTGGCTGAGCAGGGCGTCATGGCTGACAAGAACCGACTGG CAACGCTGCTCGAGAAATGGTGTTTGTGGCTGGGCAGGGCGTCATGGCTGACAAGAACCGACTGG T C SH3BP5L Ensembl:ENSG00000175137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248814159..248814734 26863196 MeRIP-seq:(Medium) rs763539800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744193,Human_RBP_ID_10896253,Human_RBP_ID_26389340,Human_RBP_ID_27799510 Human_Splice_Rec_209286,Human_Splice_Rec_209287,Human_Splice_Rec_209302,Human_Splice_Rec_209303 RMVar_hsa_circ_88240,RMVar_hsa_circ_141434,RMVar_hsa_circ_141435 97234 RMVar_ID_97234 Human_SNP_ID_57721704 m1A Human chr1 - 248825360 248825360 248825360 TATACTTGGCCTTTGTTTCTCTGCAGCTCCCCAGAGACGCTCATCCTACAGCCTCAGCTCGGGCC TATACTTGGCCTTTGTTTCTCTGCAGCTCCCCTGAGACGCTCATCCTACAGCCTCAGCTCGGGCC T A SH3BP5L Ensembl:ENSG00000175137 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:248825108..248825361 26863196 MeRIP-seq:(Medium) rs937887866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_209280 97235 RMVar_ID_97235 Human_SNP_ID_57725373 m1A Human chr1 - 248838513 248838513 248838513 CCGACTGCCTCCTCAGACACCGCGCGGTTCCCACTCAGCCGGCTGCCGACCCCCGCCTCCCGGAC CCGACTGCCTCCTCAGACACCGCGCGGTTCCCGCTCAGCCGGCTGCCGACCCCCGCCTCCCGGAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:248838284..248838519 26863196 MeRIP-seq:(Medium) rs1453308665 Functional Loss SNV dbSNP153 33..33 33 - - - 97236 RMVar_ID_97236 Human_SNP_ID_57728844 m1A Human chr1 - 248850310 248850310 248850310 AGCCCCTCAAGAGTCACCCAGTGGTCCCCTAGAGCCCTGTCCCAGCATCTCTGCCCCTGGGCCTC AGCCCCTCAAGAGTCACCCAGTGGTCCCCTAGGGCCCTGTCCCAGCATCTCTGCCCCTGGGCCTC T C ZNF692 Ensembl:ENSG00000171163 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248850260..248850462 26863196 MeRIP-seq:(Medium) rs1285099475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5109334,Human_RBP_ID_18157631 Human_miRNA_ID_1193013 97237 RMVar_ID_97237 Human_SNP_ID_57729265 m1A Human chr1 - 248851587 248851587 248851587 GAACCTAGAGTTGTGTGGATGGAGGGGGAGTGATGGGGCCAAAGGAGGAGGCTGCAGGTGTGTGT GAACCTAGAGTTGTGTGGATGGAGGGGGAGTGGTGGGGCCAAAGGAGGAGGCTGCAGGTGTGTGT T C ZNF692 Ensembl:ENSG00000171163 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:248851390..248851709 26863196 MeRIP-seq:(Medium) rs1423725561 Functional Loss SNV dbSNP153 33..33 33 - - - 97238 RMVar_ID_97238 Human_SNP_ID_57729350 m1A Human chr1 - 248851880 248851880 248851880 GGAAGATGGTGGGGCCAGTGGACTGGCCTGGAATCATGGGATTATCATAGCAAGAGGACAAGATT GGAAGATGGTGGGGCCAGTGGACTGGCCTGGAGTCATGGGATTATCATAGCAAGAGGACAAGATT T C ZNF692 Ensembl:ENSG00000171163 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:248851876..248851982 26863196 MeRIP-seq:(Medium) rs903527477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2140317,Human_RBP_ID_9412238 97239 RMVar_ID_97239 Human_SNP_ID_57729532 m1A Human chr1 - 248852696 248852696 248852696 GTGCGACAGGCCAAATGTGAGCTGAGAATAGGAGACCAGATGTGGCAGTGGTGAAGCCACCAGAT GTGCGACAGGCCAAATGTGAGCTGAGAATAGGCGACCAGATGTGGCAGTGGTGAAGCCACCAGAT T G ZNF692 Ensembl:ENSG00000171163 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248852647..248852846 26863196 MeRIP-seq:(Medium) rs1432916875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2140318,Human_RBP_ID_10896352 97240 RMVar_ID_97240 Human_SNP_ID_57730496 m1A Human chr1 + 248855943 248855943 248855943 GGGGAAGGCAGTAGTCTGGGGGCATCAGGCTCACTACTGAAAGGAGAACAAAGAGGAAGATGGCA GGGGAAGGCAGTAGTCTGGGGGCATCAGGCTCCCTACTGAAAGGAGAACAAAGAGGAAGATGGCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:248855937..248856130 26863196 MeRIP-seq:(Medium) rs1398881317 Functional Loss SNV dbSNP153 33..33 33 - - - 97241 RMVar_ID_97241 Human_SNP_ID_57731212 m1A Human chr1 - 248858200 248858200 248858200 GTGCCGCATCCGCCTGGGCGGCCACATGGAGCAGTGGTGCCTCCTCAAGGAGCGGCTGGGCTTCT GTGCCGCATCCGCCTGGGCGGCCACATGGAGCGGTGGTGCCTCCTCAAGGAGCGGCTGGGCTTCT T C ZNF692 Ensembl:ENSG00000171163 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248858151..248858325 26863196 MeRIP-seq:(Medium) rs1390321782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22871106 Human_Splice_Rec_209353,Human_Splice_Rec_209371,Human_Splice_Rec_209391,Human_Splice_Rec_209453,Human_Splice_Rec_209475,Human_Splice_Rec_209495,Human_Splice_Rec_209537,Human_Splice_Rec_209553,Human_Splice_Rec_209559,Human_Splice_Rec_209565,Human_Splice_Rec_209571,Human_Splice_Rec_209577,Human_Splice_Rec_209585,Human_Splice_Rec_209591,Human_Splice_Rec_209595,Human_Splice_Rec_209601,Human_Splice_Rec_209605 Human_miRNA_ID_845155,Human_miRNA_ID_1383797 97242 RMVar_ID_97242 Human_SNP_ID_57731221 m1A Human chr1 - 248858209 248858209 248858209 CCGCAGCAAGTGCCGCATCCGCCTGGGCGGCCACATGGAGCAGTGGTGCCTCCTCAAGGAGCGGC CCGCAGCAAGTGCCGCATCCGCCTGGGCGGCCCCATGGAGCAGTGGTGCCTCCTCAAGGAGCGGC T G ZNF692 Ensembl:ENSG00000171163 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:248858042..248858391 32194978 MeRIP-seq:(Medium) rs752088110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18569990,Human_RBP_ID_18969816,Human_RBP_ID_22871106 Human_Splice_Rec_209353,Human_Splice_Rec_209371,Human_Splice_Rec_209391,Human_Splice_Rec_209453,Human_Splice_Rec_209475,Human_Splice_Rec_209495,Human_Splice_Rec_209537,Human_Splice_Rec_209553,Human_Splice_Rec_209559,Human_Splice_Rec_209565,Human_Splice_Rec_209571,Human_Splice_Rec_209577,Human_Splice_Rec_209585,Human_Splice_Rec_209591,Human_Splice_Rec_209595,Human_Splice_Rec_209601,Human_Splice_Rec_209605 Human_miRNA_ID_845155,Human_miRNA_ID_1383797 97243 RMVar_ID_97243 Human_SNP_ID_57731404 m1A Human chr1 - 248858650 248858650 248858650 GGCCGCTGCCCTATTCAAGATGAAATGTGTGGACCGCCCCCAGCCCAGTTGAAATTTCCCGTGAA GGCCGCTGCCCTATTCAAGATGAAATGTGTGGCCCGCCCCCAGCCCAGTTGAAATTTCCCGTGAA T G ZNF692 Ensembl:ENSG00000171163 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:248858643..248859033 26863196 MeRIP-seq:(Medium) rs868827362 Functional Loss SNV dbSNP153 33..33 33 - - - 97244 RMVar_ID_97244 Human_SNP_ID_57736007 m1A Human chr1 + 248874304 248874304 248874304 TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGAAAGTAAGCCGTTTTAAAAA TTCGGCGCTCTCACCGCCGCGGCCCGGGTTCGGTTCCCGGTCAGGAAAGTAAGCCGTTTTAAAAA A G TRE-CTC2-1,tRNA-Glu-CTC-2-1 RNACentral:URS00004F5239,RNACentral:URS0000635088 tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs183759740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_349615,Human_RBP_ID_1427247,Human_RBP_ID_5273033,Human_RBP_ID_8306302,Human_RBP_ID_8968021,Human_RBP_ID_17679006,Human_RBP_ID_18174103,Human_RBP_ID_18569996,Human_RBP_ID_19449080,Human_RBP_ID_22783632,Human_RBP_ID_23111098,Human_RBP_ID_23122432 97245 RMVar_ID_97245 Human_SNP_ID_57736029 m1A Human chr1 + 248874317 248874316 248874317 CCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGAAAGTAAGCCGTTTTAAAAACTGTTGCCGCAGG CCGCCGCGGCCCGGGTTCGATTCCCGGTCAGG_AAGTAAGCCGTTTTAAAAACTGTTGCCGCAGG GA G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1182624947 Functional Loss DEL dbSNP153 33..33 33 - - - 97246 RMVar_ID_97246 Human_SNP_ID_57736032 m1A Human chr1 + 248874317 248874317 248874317 CCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGAAAGTAAGCCGTTTTAAAAACTGTTGCCGCAGG CCGCCGCGGCCCGGGTTCGATTCCCGGTCAGGGAAGTAAGCCGTTTTAAAAACTGTTGCCGCAGG A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs6672727 Functional Loss SNV dbSNP153 33..33 33 - - - 97247 RMVar_ID_97247 Human_SNP_ID_625309954 m1A Human chr17 - 45024218 45024218 45024218 CCATCCCGTCTTTGGAGTGTATCCTATTTGAGATCAAGAAATAGCCTGCTGTCCTTCCCACCTTC CCATCCCGTCTTTGGAGTGTATCCTATTTGAGGTCAAGAAATAGCCTGCTGTCCTTCCCACCTTC T C DCAKD Ensembl:ENSG00000172992 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9899209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200562,Human_RBP_ID_5115541,Human_RBP_ID_6600522,Human_RBP_ID_24479347,Human_RBP_ID_26451952 Human_miRNA_ID_1528453,Human_miRNA_ID_1537004,Human_miRNA_ID_2223421,Human_miRNA_ID_2486492,Human_miRNA_ID_3074857 RMVar_hsa_circ_82133,RMVar_hsa_circ_184782,RMVar_hsa_circ_79331,RMVar_hsa_circ_184783 97248 RMVar_ID_97248 Human_SNP_ID_625314668 m1A Human chr17 + 45042276 45042276 45042276 ACTCCCTTTACTTTCCCTCCTTTGGACTCGTCATGCTTTGGACTTTCATTTCTGTTCATGTGACT ACTCCCTTTACTTTCCCTCCTTTGGACTCGTCGTGCTTTGGACTTTCATTTCTGTTCATGTGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45042272..45042351 26863196 MeRIP-seq:(Medium) rs1427309393 Functional Loss SNV dbSNP153 33..33 33 - - - 97249 RMVar_ID_97249 Human_SNP_ID_625314765 m1A Human chr17 - 45042725 45042725 45042725 GACTTGAAGGTTTAAACAGCAACCTCTCACCAATAATGAAAGATTAGGAGTGGGGAAGCCGTATA GACTTGAAGGTTTAAACAGCAACCTCTCACCAGTAATGAAAGATTAGGAGTGGGGAAGCCGTATA T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45042718..45042841 32194978 MeRIP-seq:(Medium) rs1019725951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8454183,Human_RBP_ID_13029970 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 97250 RMVar_ID_97250 Human_SNP_ID_625316847 m1A Human chr17 + 45050480 45050480 45050480 GACCATTTAAACGTTATTTACCAAGGGGACAGATTCAGACCTTGGTGAAGACAGACAGAGGAGGA GACCATTTAAACGTTATTTACCAAGGGGACAGGTTCAGACCTTGGTGAAGACAGACAGAGGAGGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:45050443..45050569 26863196 MeRIP-seq:(Medium) rs764066998 Functional Loss SNV dbSNP153 33..33 33 - - - 97251 RMVar_ID_97251 Human_SNP_ID_625317085 m1A Human chr17 + 45051445 45051445 45051445 AAAGAGGCCCGTACGCCCCACTAGGCCGCGAAATTGGGTCGCCCGGGGCGGTGGCAGCCCCGCGT AAAGAGGCCCGTACGCCCCACTAGGCCGCGAAGTTGGGTCGCCCGGGGCGGTGGCAGCCCCGCGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45051434..45051544 26863196 MeRIP-seq:(Medium) rs992515217 Functional Loss SNV dbSNP153 33..33 33 - - - 97252 RMVar_ID_97252 Human_SNP_ID_625317112 m1A Human chr17 - 45051504 45051504 45051504 GCGGGCCGGTGAGAGCCAGCCGGGCGCCGGGGAGGGGGCGGGCCCTGGCCGCGGCTGCTACGCGG GCGGGCCGGTGAGAGCCAGCCGGGCGCCGGGGGGGGGGCGGGCCCTGGCCGCGGCTGCTACGCGG T C DCAKD Ensembl:ENSG00000172992 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45051493..45051577 26863196 MeRIP-seq:(Medium) rs998208576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419982,Human_RBP_ID_26782347 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 97253 RMVar_ID_97253 Human_SNP_ID_625317497 m1A Human chr17 + 45052080 45052051 45052080 CGGGCGGGCGGACGCGGGAGAGGTTGGGCGGGAGAGGTTGGGCGGGAGGGCGGCCGGACGGACGC CGGG_____________________________GAGGTTGGGCGGGAGGGCGGCCGGACGGACGC GCGGGCGGACGCGGGAGAGGTTGGGCGGGA G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45052078..45052213 26863196 MeRIP-seq:(Medium) rs1555602125 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_3542997,Human_RBP_ID_8189680,Human_RBP_ID_9424034 97254 RMVar_ID_97254 Human_SNP_ID_625317523 m1A Human chr17 + 45052080 45052080 45052080 CGGGCGGGCGGACGCGGGAGAGGTTGGGCGGGAGAGGTTGGGCGGGAGGGCGGCCGGACGGACGC CGGGCGGGCGGACGCGGGAGAGGTTGGGCGGGCGAGGTTGGGCGGGAGGGCGGCCGGACGGACGC A C NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45052078..45052213 26863196 MeRIP-seq:(Medium) rs1192459690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542997,Human_RBP_ID_8189680,Human_RBP_ID_9424034 97255 RMVar_ID_97255 Human_SNP_ID_625317539 m1A Human chr17 + 45052105 45052105 45052105 GGGCGGGAGAGGTTGGGCGGGAGGGCGGCCGGACGGACGCGGGAGAGGCCGGCGGGGAGAGCTCG GGGCGGGAGAGGTTGGGCGGGAGGGCGGCCGGGCGGACGCGGGAGAGGCCGGCGGGGAGAGCTCG A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45052093..45052196 26863196 MeRIP-seq:(Medium) rs1311698589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542997,Human_RBP_ID_8189680,Human_RBP_ID_9424034 97256 RMVar_ID_97256 Human_SNP_ID_625320224 m1A Human chr17 - 45061376 45061376 45061376 GGCCGTTCCCGTTCCCTTCCATCATCTGCGGCAGCGGAGGTGCCGGCGGCTTCACTGCTGTCTCA GGCCGTTCCCGTTCCCTTCCATCATCTGCGGCCGCGGAGGTGCCGGCGGCTTCACTGCTGTCTCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr17:45061326..45061400;chr17:45061326..45061375 26863196 MeRIP-seq:(Medium) rs772038652 Functional Loss SNV dbSNP153 33..33 33 - - - 97257 RMVar_ID_97257 Human_SNP_ID_625326556 m1A Human chr17 + 45086579 45086579 45086579 AAGGCCATTGAGCTGTTCTCAGTGGGTCAGGGACCTGCCAAAACCATGGAGGAGGCTAGCAAGCG AAGGCCATTGAGCTGTTCTCAGTGGGTCAGGGCCCTGCCAAAACCATGGAGGAGGCTAGCAAGCG A C NMT1 Ensembl:ENSG00000136448 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45086464..45086694 26863196 MeRIP-seq:(Medium) rs746348189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236247,Human_RBP_ID_1008537,Human_RBP_ID_1859717,Human_RBP_ID_3525041,Human_RBP_ID_3950749,Human_RBP_ID_8818651,Human_RBP_ID_9376212,Human_RBP_ID_17893757,Human_RBP_ID_18470063,Human_RBP_ID_26331951,Human_RBP_ID_27812784 Human_Splice_Rec_1827896,Human_Splice_Rec_1827897,Human_Splice_Rec_1827914,Human_Splice_Rec_1827918,Human_Splice_Rec_1827919,Human_Splice_Rec_1827938,Human_Splice_Rec_1827939,Human_Splice_Rec_1827950,Human_Splice_Rec_1827951,Human_Splice_Rec_1827960,Human_Splice_Rec_1827961,Human_Splice_Rec_1827970,Human_Splice_Rec_1827971 Human_miRNA_ID_3001964 RMVar_hsa_circ_92906,RMVar_hsa_circ_338898,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_271884,RMVar_hsa_circ_184790,RMVar_hsa_circ_361836,RMVar_hsa_circ_184791 97258 RMVar_ID_97258 Human_SNP_ID_625330579 m1A Human chr17 + 45102739 45102735 45102739 AGGGAGTCAGCCTGGGGCCATGTAGATGGTTGATTGATGTAGCAGTCTGAGTCTGCCTGGACTAG AGGGAGTCAGCCTGGGGCCATGTAGATGG____TTGATGTAGCAGTCTGAGTCTGCCTGGACTAG GTTGA G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45102734..45102805 26863196 MeRIP-seq:(Medium) rs1165179131 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13031338,Human_RBP_ID_24552197 RMVar_hsa_circ_110318,RMVar_hsa_circ_184793 97259 RMVar_ID_97259 Human_SNP_ID_625333046 m1A Human chr17 - 45112179 45112179 45112179 CCACTTGGCCCCGACCCCGAGCTTAGCCCCTAAGCCCTCCTTTACCCCAGGCCTTCCTGGACTCC CCACTTGGCCCCGACCCCGAGCTTAGCCCCTAGGCCCTCCTTTACCCCAGGCCTTCCTGGACTCC T C PLCD3 Ensembl:ENSG00000161714 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:45112001..45112231 26863196 MeRIP-seq:(Medium) rs1251795144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767226,Human_RBP_ID_17080693,Human_RBP_ID_18943288,Human_RBP_ID_27453322 97260 RMVar_ID_97260 Human_SNP_ID_625333059 m1A Human chr17 + 45112212 45112212 45112212 TAGGGGCTAAGCTCGGGGTCGGGGCCAAGTGGAGTGACTGCGCTCCTCTGGGGGAAGGAGGCTGG TAGGGGCTAAGCTCGGGGTCGGGGCCAAGTGGGGTGACTGCGCTCCTCTGGGGGAAGGAGGCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45111934..45112696 26863196 MeRIP-seq:(Medium) rs1025629043 Functional Loss SNV dbSNP153 33..33 33 - - - 97261 RMVar_ID_97261 Human_SNP_ID_625333072 m1A Human chr17 + 45112261 45112261 45112261 GGGGGAAGGAGGCTGGGATGGCCCACGGGAGGACAGAGGGGAACTGAGGGCCCACAAGTGTCCTG GGGGGAAGGAGGCTGGGATGGCCCACGGGAGGCCAGAGGGGAACTGAGGGCCCACAAGTGTCCTG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:45112211..45112312;chr17:45112211..45112511 32194978 MeRIP-seq:(Medium) rs746625861 Functional Loss SNV dbSNP153 33..33 33 - - - 97262 RMVar_ID_97262 Human_SNP_ID_625333550 m1A Human chr17 - 45113489 45113489 45113489 TAAAACCTGCCTGCCTGCGGCAACCTGACTCGACCTTTGACCCCGAGTACCCAGGACCTCCCAGA TAAAACCTGCCTGCCTGCGGCAACCTGACTCGCCCTTTGACCCCGAGTACCCAGGACCTCCCAGA T G PLCD3 Ensembl:ENSG00000161714 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45113410..45113548 26863196 MeRIP-seq:(Medium) rs756122111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828011,Human_Splice_Rec_1828017,Human_Splice_Rec_1828024,Human_Splice_Rec_1828025 97263 RMVar_ID_97263 Human_SNP_ID_625334053 m1A Human chr17 + 45115170 45115163 45115170 CTGACCTGGCAGGGTTGTGGGGCGTTGGGGGCAGGGTGCAGGGTCCGCAGGCGGGTGGCGTGGCA CTGACCTGGCAGGGTTGTGGGGCGTT_______GGGTGCAGGGTCCGCAGGCGGGTGGCGTGGCA TGGGGGCA T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:45115151..45115175 26863196 MeRIP-seq:(Medium) rs1175915805 Functional Loss DEL dbSNP153 27..33 33 - - - 97264 RMVar_ID_97264 Human_SNP_ID_625334185 m1A Human chr17 - 45115377 45115374 45115377 GAGGAGGAGGAGGAGGATGACGAGGAGGAAGAAGAGGAGGTGGAGGCTGCAGCGCAGAGGCGGCT GAGGAGGAGGAGGAGGATGACGAGGAGGAAGA___GGAGGTGGAGGCTGCAGCGCAGAGGCGGCT CTCT C PLCD3 Ensembl:ENSG00000161714 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45114354..45115556 26863196 MeRIP-seq:(Medium) rs764837403 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_822329,Human_RBP_ID_5577385,Human_RBP_ID_18988654 Human_Splice_Rec_1828005,Human_Splice_Rec_1828035,Human_Splice_Rec_1828043 RMVar_hsa_circ_79873,RMVar_hsa_circ_95837,RMVar_hsa_circ_184796,RMVar_hsa_circ_184797 97265 RMVar_ID_97265 Human_SNP_ID_625334232 m1A Human chr17 + 45115474 45115474 45115474 GAGCAGCGGGCAACTTCTTTCCCTTCACCAGGACCCGGCCCTTCAGCTGCTGTGGGGGCCAACGT GAGCAGCGGGCAACTTCTTTCCCTTCACCAGGTCCCGGCCCTTCAGCTGCTGTGGGGGCCAACGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45115427..45115578 32194978 MeRIP-seq:(Medium) rs761029644 Functional Loss SNV dbSNP153 33..33 33 - - - 97266 RMVar_ID_97266 Human_SNP_ID_625334623 m1A Human chr17 + 45116776 45116776 45116776 CAGTGGTTCTCCAGGGATAGGATGACAGGGTAAGGGGACAGCTGTGGGGGGAAGGGCAGCAGCTC CAGTGGTTCTCCAGGGATAGGATGACAGGGTACGGGGACAGCTGTGGGGGGAAGGGCAGCAGCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45116599..45116800 26863196 MeRIP-seq:(Medium) rs1460463843 Functional Loss SNV dbSNP153 33..33 33 - - - 97267 RMVar_ID_97267 Human_SNP_ID_625335909 m1A Human chr17 - 45120951 45120951 45120951 AGGAAGCGCAGCGCTGGGTGCGCGGTCTGACCAAGCTCCGCGCGCGCCTGGACGCCATGAGCCAG AGGAAGCGCAGCGCTGGGTGCGCGGTCTGACCCAGCTCCGCGCGCGCCTGGACGCCATGAGCCAG T G PLCD3 Ensembl:ENSG00000161714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:45120402..45120950 26863410 MeRIP-seq:(Medium) rs1194623602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126906,RMVar_hsa_circ_318419,RMVar_hsa_circ_101263,RMVar_hsa_circ_92261,RMVar_hsa_circ_184800,RMVar_hsa_circ_184801,RMVar_hsa_circ_117902,RMVar_hsa_circ_184803,RMVar_hsa_circ_122820,RMVar_hsa_circ_184804,RMVar_hsa_circ_308612,RMVar_hsa_circ_184805,RMVar_hsa_circ_184806 97268 RMVar_ID_97268 Human_SNP_ID_625336135 m1A Human chr17 + 45121342 45121342 45121342 AGCGGATCTTGCGGAGCCGGGAGCCCCGCAGCATGGCGCGCACGTCCTCGTCCTCCGTCAGGCCT AGCGGATCTTGCGGAGCCGGGAGCCCCGCAGCGTGGCGCGCACGTCCTCGTCCTCCGTCAGGCCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:45121228..45129248 26863410 MeRIP-seq:(Medium) rs766334483 Functional Loss SNV dbSNP153 33..33 33 - - - 97269 RMVar_ID_97269 Human_SNP_ID_625337802 m1A Human chr17 - 45127732 45127732 45127732 CACGCACACACACACTCCCCACCTATGCATACACCCCACACACACCCTGCCCTGCCTGCATGCCA CACGCACACACACACTCCCCACCTATGCATACCCCCCACACACACCCTGCCCTGCCTGCATGCCA T G PLCD3 Ensembl:ENSG00000161714 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45127729..45127930 26863196 MeRIP-seq:(Medium) rs931207007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200567,Human_RBP_ID_24531949 RMVar_hsa_circ_101263,RMVar_hsa_circ_184800 97270 RMVar_ID_97270 Human_SNP_ID_625338428 m1A Human chr17 - 45130459 45130459 45130459 CGGGTGCCGCGGAAGGGCTGAGGGGAGGCCCCATGCCCATTGGCCTCTTCATCCCACACGTTTGC CGGGTGCCGCGGAAGGGCTGAGGGGAGGCCCCTTGCCCATTGGCCTCTTCATCCCACACGTTTGC T A PLCD3 Ensembl:ENSG00000161714 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45130457..45130955 26863196 MeRIP-seq:(Medium) rs1206907842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6600876,Human_RBP_ID_8189685 RMVar_hsa_circ_101263,RMVar_hsa_circ_184800 97271 RMVar_ID_97271 Human_SNP_ID_625338429 m1A Human chr17 - 45130459 45130459 45130459 CGGGTGCCGCGGAAGGGCTGAGGGGAGGCCCCATGCCCATTGGCCTCTTCATCCCACACGTTTGC CGGGTGCCGCGGAAGGGCTGAGGGGAGGCCCCGTGCCCATTGGCCTCTTCATCCCACACGTTTGC T C PLCD3 Ensembl:ENSG00000161714 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45130457..45130955 26863196 MeRIP-seq:(Medium) rs1206907842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6600876,Human_RBP_ID_8189685 RMVar_hsa_circ_101263,RMVar_hsa_circ_184800 97272 RMVar_ID_97272 Human_SNP_ID_625338543 m1A Human chr17 - 45130921 45130921 45130921 ACAAAGGAACAGGACCTTGGGGGTGGGGGAACAGGGGGCAGCACATGAGGGGCTGGGGAGCCAGC ACAAAGGAACAGGACCTTGGGGGTGGGGGAACGGGGGGCAGCACATGAGGGGCTGGGGAGCCAGC T C PLCD3 Ensembl:ENSG00000161714 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:45130795..45130942 26863196 MeRIP-seq:(Medium) rs991266126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6600877,Human_RBP_ID_8189687 RMVar_hsa_circ_101263,RMVar_hsa_circ_184800 97273 RMVar_ID_97273 Human_SNP_ID_625338896 m1A Human chr17 + 45132406 45132406 45132406 GCGGGCGGCGGCAACGCCTCCAGCGGCCGCACAGCATGGCTTGGCGGGGGGCCGGGGCCGGGCCC GCGGGCGGCGGCAACGCCTCCAGCGGCCGCACGGCATGGCTTGGCGGGGGGCCGGGGCCGGGCCC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:45132301..45132525 26863410 MeRIP-seq:(Medium) rs1233434065 Functional Loss SNV dbSNP153 33..33 33 - - - 97274 RMVar_ID_97274 Human_SNP_ID_625340308 m1A Human chr17 + 45137086 45137086 45137086 GGACATGTTTGGTTACTTCGAGCCCCTGTACCAGGTGATCCCTGACATGCCGAGGCCCCCAGAGA GGACATGTTTGGTTACTTCGAGCCCCTGTACCGGGTGATCCCTGACATGCCGAGGCCCCCAGAGA A G ACBD4 Ensembl:ENSG00000181513 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45137036..45137414 32194978 MeRIP-seq:(Medium) rs1289110869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18988660,Human_RBP_ID_22062715 Human_Splice_Rec_1828080,Human_Splice_Rec_1828081,Human_Splice_Rec_1828102,Human_Splice_Rec_1828103,Human_Splice_Rec_1828130,Human_Splice_Rec_1828131,Human_Splice_Rec_1828148,Human_Splice_Rec_1828149,Human_Splice_Rec_1828162,Human_Splice_Rec_1828163,Human_Splice_Rec_1828178,Human_Splice_Rec_1828179,Human_Splice_Rec_1828194,Human_Splice_Rec_1828195,Human_Splice_Rec_1828204,Human_Splice_Rec_1828205,Human_Splice_Rec_1828220,Human_Splice_Rec_1828221,Human_Splice_Rec_1828238,Human_Splice_Rec_1828239,Human_Splice_Rec_1828252,Human_Splice_Rec_1828253,Human_Splice_Rec_1828258,Human_Splice_Rec_1828259,Human_Splice_Rec_1828268,Human_Splice_Rec_1828269 RMVar_hsa_circ_11668,RMVar_hsa_circ_56857 97275 RMVar_ID_97275 Human_SNP_ID_625343529 m1A Human chr17 + 45148565 45148565 45148565 CGGAAGAGGAGCTGTGGGAAGGGGGAGGAGGGAGGGAGGAAAAGAGGAGGAGGCGGAGGAGAACT CGGAAGAGGAGCTGTGGGAAGGGGGAGGAGGGGGGGAGGAAAAGAGGAGGAGGCGGAGGAGAACT A G HEXIM1 Ensembl:ENSG00000186834 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:45148525..45148657 26863196 MeRIP-seq:(Medium) rs1357560102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767574,Human_RBP_ID_1546657,Human_RBP_ID_2529682,Human_RBP_ID_3541721,Human_RBP_ID_3952565,Human_RBP_ID_4464617,Human_RBP_ID_5088254,Human_RBP_ID_5143256,Human_RBP_ID_8192041,Human_RBP_ID_8232026,Human_RBP_ID_8941826,Human_RBP_ID_9422360,Human_RBP_ID_17068130,Human_RBP_ID_17669960,Human_RBP_ID_18420500,Human_RBP_ID_18941780,Human_RBP_ID_22063181,Human_RBP_ID_22717441,Human_RBP_ID_22952258,Human_RBP_ID_23118764,Human_RBP_ID_24552303,Human_RBP_ID_26963195 97276 RMVar_ID_97276 Human_SNP_ID_625343545 m1A Human chr17 + 45148602 45148597 45148602 GGAAAAGAGGAGGAGGCGGAGGAGAACTGAGCAGAGCAGAGCATCGAGCCAAAGGGGAGATGAGT GGAAAAGAGGAGGAGGCGGAGGAGAACT_____GAGCAGAGCATCGAGCCAAAGGGGAGATGAGT TGAGCA T HEXIM1 Ensembl:ENSG00000186834 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45148476..45149433 26863196 MeRIP-seq:(Medium) rs982605629 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_897672,Human_RBP_ID_1546657,Human_RBP_ID_3541722,Human_RBP_ID_3950754,Human_RBP_ID_4464617,Human_RBP_ID_5088254,Human_RBP_ID_5143256,Human_RBP_ID_6600910,Human_RBP_ID_8192041,Human_RBP_ID_8232026,Human_RBP_ID_8941826,Human_RBP_ID_9422360,Human_RBP_ID_17653859,Human_RBP_ID_17669960,Human_RBP_ID_18419629,Human_RBP_ID_18544410,Human_RBP_ID_18941780,Human_RBP_ID_22061419,Human_RBP_ID_22357302,Human_RBP_ID_22523793,Human_RBP_ID_22717441,Human_RBP_ID_23118764,Human_RBP_ID_24545021,Human_RBP_ID_24552303,Human_RBP_ID_26331957,Human_RBP_ID_26769319,Human_RBP_ID_27812787 97277 RMVar_ID_97277 Human_SNP_ID_625343548 m1A Human chr17 + 45148602 45148602 45148602 GGAAAAGAGGAGGAGGCGGAGGAGAACTGAGCAGAGCAGAGCATCGAGCCAAAGGGGAGATGAGT GGAAAAGAGGAGGAGGCGGAGGAGAACTGAGCGGAGCAGAGCATCGAGCCAAAGGGGAGATGAGT A G HEXIM1 Ensembl:ENSG00000186834 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45148476..45149433 26863196 MeRIP-seq:(Medium) rs1471230098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897672,Human_RBP_ID_1546657,Human_RBP_ID_3541722,Human_RBP_ID_3950754,Human_RBP_ID_4464617,Human_RBP_ID_5088254,Human_RBP_ID_5143256,Human_RBP_ID_6600910,Human_RBP_ID_8192041,Human_RBP_ID_8232026,Human_RBP_ID_8941826,Human_RBP_ID_9422360,Human_RBP_ID_17653859,Human_RBP_ID_17669960,Human_RBP_ID_18419629,Human_RBP_ID_18544410,Human_RBP_ID_18941780,Human_RBP_ID_22061419,Human_RBP_ID_22357302,Human_RBP_ID_22523793,Human_RBP_ID_22717441,Human_RBP_ID_23118764,Human_RBP_ID_24545021,Human_RBP_ID_24552303,Human_RBP_ID_26331957,Human_RBP_ID_26769319,Human_RBP_ID_27812787 97278 RMVar_ID_97278 Human_SNP_ID_625343670 m1A Human chr17 - 45148941 45148941 45148941 AGTGCGGCCAGCTAGCGGGTCCAAGGGGGTGCAGCGGCAGGAACAGTACGTAATGGGCGGAGGTG AGTGCGGCCAGCTAGCGGGTCCAAGGGGGTGCGGCGGCAGGAACAGTACGTAATGGGCGGAGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45148891..45149027 26863196 MeRIP-seq:(Medium) rs1470990510 Functional Loss SNV dbSNP153 33..33 33 - - - 97279 RMVar_ID_97279 Human_SNP_ID_625343674 m1A Human chr17 - 45148950 45148950 45148950 AGCGCCCACAGTGCGGCCAGCTAGCGGGTCCAAGGGGGTGCAGCGGCAGGAACAGTACGTAATGG AGCGCCCACAGTGCGGCCAGCTAGCGGGTCCAGGGGGGTGCAGCGGCAGGAACAGTACGTAATGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45148651..45148952 32194978 MeRIP-seq:(Medium) rs752493115 Functional Loss SNV dbSNP153 33..33 33 - - - 97280 RMVar_ID_97280 Human_SNP_ID_625343938 m1A Human chr17 + 45149524 45149524 45149524 GCGACTTCCCGCCGCCGGCAGAAGTGGAACCGACGCCCGAGGCCGAGCTGCTCGCCCAGCCTTGT GCGACTTCCCGCCGCCGGCAGAAGTGGAACCGGCGCCCGAGGCCGAGCTGCTCGCCCAGCCTTGT A G HEXIM1 Ensembl:ENSG00000186834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:45149476..45149575 26863196 MeRIP-seq:(Medium) rs756767765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50973,Human_RBP_ID_1286775,Human_RBP_ID_4432566,Human_RBP_ID_22063185 97281 RMVar_ID_97281 Human_SNP_ID_625347748 m1A Human chr17 + 45162001 45161998 45162001 ACAGGCAGTCGCACAGAAAGGCACACAGATGTAGTGGTGTGCATAGCCCTTGACAGCGAATAGGT ACAGGCAGTCGCACAGAAAGGCACACAGAT___GTGGTGTGCATAGCCCTTGACAGCGAATAGGT TGTA T HEXIM2 Ensembl:ENSG00000168517 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45161958..45162033 26863196 MeRIP-seq:(Medium) rs990555591 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8454307,Human_RBP_ID_18419632 Human_Splice_Rec_1828299,Human_Splice_Rec_1828315 97282 RMVar_ID_97282 Human_SNP_ID_625349679 m1A Human chr17 + 45169191 45169191 45169191 AGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCAGCGGAGGCTGTGCTGGCCCGGAAGAAACACCG AGTCCCCGGACCCAGAGCCCAGGGGGCTGCTCGGCGGAGGCTGTGCTGGCCCGGAAGAAACACCG A G HEXIM2 Ensembl:ENSG00000168517 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45161973..45169296 32194978 MeRIP-seq:(Medium) rs911858855 Functional Loss SNV dbSNP153 33..33 33 - - - 97283 RMVar_ID_97283 Human_SNP_ID_625363582 m1A Human chr17 - 45221487 45221487 45221487 GGCGAGGGATTGGCCGGGTCTGGGTGAAGGGGATCACGGCCTGGGGATTGGAGGGGCACATCTTC GGCGAGGGATTGGCCGGGTCTGGGTGAAGGGGGTCACGGCCTGGGGATTGGAGGGGCACATCTTC T C AC008105.3 Ensembl:ENSG00000267121 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45221329..45221627 32194978 MeRIP-seq:(Medium) rs1370370614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546837,Human_RBP_ID_3547448,Human_RBP_ID_5188652,Human_RBP_ID_5579693,Human_RBP_ID_5649178,Human_RBP_ID_9422901 Human_miRNA_ID_3164848 97284 RMVar_ID_97284 Human_SNP_ID_625363583 m1A Human chr17 - 45221487 45221487 45221487 GGCGAGGGATTGGCCGGGTCTGGGTGAAGGGGATCACGGCCTGGGGATTGGAGGGGCACATCTTC GGCGAGGGATTGGCCGGGTCTGGGTGAAGGGGCTCACGGCCTGGGGATTGGAGGGGCACATCTTC T G AC008105.3 Ensembl:ENSG00000267121 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45221329..45221627 32194978 MeRIP-seq:(Medium) rs1370370614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546837,Human_RBP_ID_3547448,Human_RBP_ID_5188652,Human_RBP_ID_5579693,Human_RBP_ID_5649178,Human_RBP_ID_9422901 Human_miRNA_ID_3164848 97285 RMVar_ID_97285 Human_SNP_ID_625363793 m1A Human chr17 - 45222065 45222065 45222065 CCTCCAGCCTCGGAAATCCAGCTTTCCGGGGGACGGGGACGAGGCTCCCGGCCCGGGCGGGGGCG CCTCCAGCCTCGGAAATCCAGCTTTCCGGGGGGCGGGGACGAGGCTCCCGGCCCGGGCGGGGGCG T C AC008105.3 Ensembl:ENSG00000267121 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45221924..45230637 32194978 MeRIP-seq:(Medium) rs911315167 Functional Loss SNV dbSNP153 33..33 33 - - - 97286 RMVar_ID_97286 Human_SNP_ID_625363796 m1A Human chr17 + 45222075 45222075 45222075 CGGGCCGGGAGCCTCGTCCCCGTCCCCCGGAAAGCTGGATTTCCGAGGCTGGAGGCGCCTGGCCG CGGGCCGGGAGCCTCGTCCCCGTCCCCCGGAAGGCTGGATTTCCGAGGCTGGAGGCGCCTGGCCG A G FMNL1 Ensembl:ENSG00000184922 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:45221601..45222250 26863196 MeRIP-seq:(Medium) rs942813966 Functional Loss SNV dbSNP153 33..33 33 - - - 97287 RMVar_ID_97287 Human_SNP_ID_625367645 m1A Human chr17 + 45237341 45237339 45237342 CAGCCTGTGTCAATGAGATTGCTCTGAGCCTCAACAACAAGAACCCCAGGTGAGGTCCAGGCCCC CAGCCTGTGTCAATGAGATTGCTCTGAGCCT___CAACAAGAACCCCAGGTGAGGTCCAGGCCCC TCAA T FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45237290..45237579 32194978 MeRIP-seq:(Medium) rs1172737094 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_27812790 Human_Splice_Rec_1828354,Human_Splice_Rec_1828355,Human_Splice_Rec_1828446,Human_Splice_Rec_1828447,Human_Splice_Rec_1828458,Human_Splice_Rec_1828459 RMVar_hsa_circ_87550,RMVar_hsa_circ_10057,RMVar_hsa_circ_103187,RMVar_hsa_circ_93557,RMVar_hsa_circ_184811,RMVar_hsa_circ_184812,RMVar_hsa_circ_108899,RMVar_hsa_circ_272746,RMVar_hsa_circ_184814,RMVar_hsa_circ_184815,RMVar_hsa_circ_184813 97288 RMVar_ID_97288 Human_SNP_ID_625368746 m1A Human chr17 + 45241583 45241583 45241583 TCGAGATCCTCCCCGTCGCTGTGGCAACTCCGAGCGGCGGTGATGCTCCGACTCCGGGGGTGCCG TCGAGATCCTCCCCGTCGCTGTGGCAACTCCGGGCGGCGGTGATGCTCCGACTCCGGGGGTGCCG A G FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45241390..45241675 26863196 MeRIP-seq:(Medium) rs781102841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828367,Human_Splice_Rec_1828401,Human_Splice_Rec_1828489 RMVar_hsa_circ_103187,RMVar_hsa_circ_184812,RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97289 RMVar_ID_97289 Human_SNP_ID_625368881 m1A Human chr17 - 45241918 45241918 45241918 TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGAGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGGGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45241870..45242022 32194978 MeRIP-seq:(Medium) rs1483850863 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 97290 RMVar_ID_97290 Human_SNP_ID_625368882 m1A Human chr17 - 45241918 45241918 45241918 TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGAGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGCGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45241870..45242022 32194978 MeRIP-seq:(Medium) rs1483850863 Functional Loss SNV dbSNP153 33..33 33 - - - 97291 RMVar_ID_97291 Human_SNP_ID_625368883 m1A Human chr17 - 45241918 45241918 45241918 TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGAGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG TGGGGGCGCAGAGGGCGGGGCTTCCTGCGGGGTGGGGAGGCCGGGCAGTGGGGGCGGCGGCGGTG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45241870..45242022 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 97292 RMVar_ID_97292 Human_SNP_ID_625368959 m1A Human chr17 - 45242067 45242064 45242067 CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCACCGGCCCGTCAGTGCCCGGAGGTGGTGG CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGG___CACCGGCCCGTCAGTGCCCGGAGGTGGTGG GCCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45241826..45242150 26863196 MeRIP-seq:(Medium) rs1275514181 Functional Loss DEL dbSNP153 33..35 33 - - - 97293 RMVar_ID_97293 Human_SNP_ID_625368971 m1A Human chr17 - 45242067 45242067 45242067 CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCACCGGCCCGTCAGTGCCCGGAGGTGGTGG CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGGGGCACCGGCCCGTCAGTGCCCGGAGGTGGTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45241826..45242150 26863196 MeRIP-seq:(Medium) rs1290702799 Functional Loss SNV dbSNP153 33..33 33 - - - 97294 RMVar_ID_97294 Human_SNP_ID_625368972 m1A Human chr17 - 45242067 45242067 45242067 CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGAGGCACCGGCCCGTCAGTGCCCGGAGGTGGTGG CCGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCACCGGCCCGTCAGTGCCCGGAGGTGGTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45241826..45242150 26863196 MeRIP-seq:(Medium) rs1290702799 Functional Loss SNV dbSNP153 33..33 33 - - - 97295 RMVar_ID_97295 Human_SNP_ID_625368999 m1A Human chr17 + 45242100 45242100 45242100 CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGAGGTCCTCCTGATGCCCTAGGAAGACGCGACTC CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGCGGTCCTCCTGATGCCCTAGGAAGACGCGACTC A C FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:45242051..45242125;chr17:45241849..45242115 26863196 MeRIP-seq:(Medium) rs530661621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828369,Human_Splice_Rec_1828403,Human_Splice_Rec_1828467,Human_Splice_Rec_1828491 RMVar_hsa_circ_103187,RMVar_hsa_circ_184812,RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97296 RMVar_ID_97296 Human_SNP_ID_625369000 m1A Human chr17 + 45242100 45242100 45242100 CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGAGGTCCTCCTGATGCCCTAGGAAGACGCGACTC CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGGGGTCCTCCTGATGCCCTAGGAAGACGCGACTC A G FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:45242051..45242125;chr17:45241849..45242115 26863196 MeRIP-seq:(Medium) rs530661621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828369,Human_Splice_Rec_1828403,Human_Splice_Rec_1828467,Human_Splice_Rec_1828491 RMVar_hsa_circ_103187,RMVar_hsa_circ_184812,RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97297 RMVar_ID_97297 Human_SNP_ID_625369001 m1A Human chr17 + 45242100 45242100 45242100 CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGAGGTCCTCCTGATGCCCTAGGAAGACGCGACTC CCGCCGCCGCCGCCGCCGCCGCCGCCTCCCGGTGGTCCTCCTGATGCCCTAGGAAGACGCGACTC A T FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:45242051..45242125;chr17:45241849..45242115 26863196 MeRIP-seq:(Medium) rs530661621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828369,Human_Splice_Rec_1828403,Human_Splice_Rec_1828467,Human_Splice_Rec_1828491 RMVar_hsa_circ_103187,RMVar_hsa_circ_184812,RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97298 RMVar_ID_97298 Human_SNP_ID_625369308 m1A Human chr17 + 45243165 45243165 45243165 GATTTTGAGGAACAGTTCAAGACCAAGTCCCAAGGCCCCAGCCTGGACCTCAGCGCTCTCAAGAG GATTTTGAGGAACAGTTCAAGACCAAGTCCCAGGGCCCCAGCCTGGACCTCAGCGCTCTCAAGAG A G FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:45242464..45243936 32194978 MeRIP-seq:(Medium) rs1333052954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828372,Human_Splice_Rec_1828406,Human_Splice_Rec_1828470,Human_Splice_Rec_1828494 RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97299 RMVar_ID_97299 Human_SNP_ID_625369513 m1A Human chr17 + 45243900 45243900 45243900 TCATCACCCGCTTTGAGCGGGAGCAGCGGCCAATGGAGGAGCTGTCAGAGGAGGACCGCTTCATG TCATCACCCGCTTTGAGCGGGAGCAGCGGCCAGTGGAGGAGCTGTCAGAGGAGGACCGCTTCATG A G FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45243849..45244025 26863196 MeRIP-seq:(Medium) rs201146629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108899,RMVar_hsa_circ_184815,RMVar_hsa_circ_119869,RMVar_hsa_circ_184817 97300 RMVar_ID_97300 Human_SNP_ID_625370277 m1A Human chr17 + 45246264 45246264 45246264 CACAGATGGACCTCATCTCTGAGCTGAAACGGAGGCAGCAGAAGGAGCCACTCATTTATGAGAGC CACAGATGGACCTCATCTCTGAGCTGAAACGGCGGCAGCAGAAGGAGCCACTCATTTATGAGAGC A C FMNL1 Ensembl:ENSG00000184922 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45246208..45246299 26863196 MeRIP-seq:(Medium) rs771937462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828388,Human_Splice_Rec_1828389,Human_Splice_Rec_1828422,Human_Splice_Rec_1828423,Human_Splice_Rec_1828484,Human_Splice_Rec_1828510,Human_Splice_Rec_1828511,Human_Splice_Rec_1828528,Human_Splice_Rec_1828534 RMVar_hsa_circ_10124,RMVar_hsa_circ_56701 97301 RMVar_ID_97301 Human_SNP_ID_625370314 m1A Human chr17 - 45246373 45246371 45246374 GGATAGCGCATTGGGTCAGAAGAAAGCATAGAAGGACAGACTGAGGATAAGACCAAGGCCTGGCC GGATAGCGCATTGGGTCAGAAGAAAGCATAG___GACAGACTGAGGATAAGACCAAGGCCTGGCC CCTT C AC008105.2 Ensembl:ENSG00000233483 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45246368..45246600 26863196 MeRIP-seq:(Medium) rs1241732295 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5578402,Human_RBP_ID_13031776,Human_RBP_ID_17207191 97302 RMVar_ID_97302 Human_SNP_ID_625370653 m1A Human chr17 - 45247446 45247446 45247446 AGCGGGCTCCCTCGCCGCCAACTCTAGTGAAGAAGCAGCCCTTCTCCCCGGCGCCCGCTGGTTTG AGCGGGCTCCCTCGCCGCCAACTCTAGTGAAGGAGCAGCCCTTCTCCCCGGCGCCCGCTGGTTTG T C AC008105.2 Ensembl:ENSG00000233483 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45247396..45247494 26863196 MeRIP-seq:(Medium) rs1043793610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828542,Human_Splice_Rec_1828543,Human_Splice_Rec_1828546 97303 RMVar_ID_97303 Human_SNP_ID_625370654 m1A Human chr17 - 45247446 45247446 45247446 AGCGGGCTCCCTCGCCGCCAACTCTAGTGAAGAAGCAGCCCTTCTCCCCGGCGCCCGCTGGTTTG AGCGGGCTCCCTCGCCGCCAACTCTAGTGAAGCAGCAGCCCTTCTCCCCGGCGCCCGCTGGTTTG T G AC008105.2 Ensembl:ENSG00000233483 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45247396..45247494 26863196 MeRIP-seq:(Medium) rs1043793610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828542,Human_Splice_Rec_1828543,Human_Splice_Rec_1828546 97304 RMVar_ID_97304 Human_SNP_ID_625380552 m1A Human chr17 - 45286750 45286750 45286750 CCCATTCCACCCTCTCCAGCCCTGGAAACCTCACCCTCTGGAGTCCTTCCTGGGCAAACTGGCCT CCCATTCCACCCTCTCCAGCCCTGGAAACCTCGCCCTCTGGAGTCCTTCCTGGGCAAACTGGCCT T C MAP3K14 Ensembl:ENSG00000006062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45286700..45286864 26863196 MeRIP-seq:(Medium) rs779741662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897673,Human_RBP_ID_5129598,Human_RBP_ID_17079628,Human_RBP_ID_18943290,Human_RBP_ID_26452029,Human_RBP_ID_27453383 RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741,RMVar_hsa_circ_34270,RMVar_hsa_circ_337826 97305 RMVar_ID_97305 Human_SNP_ID_625381515 m1A Human chr17 - 45290577 45290577 45290577 AGAAGAGCCCTGTGTTCTGCGGAAAGTGGGAGATCCTGAATGACGTGATTACCAAGGGCACAGCC AGAAGAGCCCTGTGTTCTGCGGAAAGTGGGAGGTCCTGAATGACGTGATTACCAAGGGCACAGCC T C MAP3K14 Ensembl:ENSG00000006062 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:45290404..45290582 26863196 MeRIP-seq:(Medium) rs772671564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1859796 Human_Splice_Rec_1828659,Human_Splice_Rec_1828687,Human_Splice_Rec_1828745 RMVar_hsa_circ_11822,RMVar_hsa_circ_28319,RMVar_hsa_circ_34270,RMVar_hsa_circ_337479 97306 RMVar_ID_97306 Human_SNP_ID_625387206 m1A Human chr17 - 45316815 45316815 45316815 AGTGGGGTCGGCGGCCAGGCCAGCGCAGTCCGACGTACCCCGTCCAACCCACTCGCAGCGGTCCG AGTGGGGTCGGCGGCCAGGCCAGCGCAGTCCGCCGTACCCCGTCCAACCCACTCGCAGCGGTCCG T G MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45316812..45317027 26863196 MeRIP-seq:(Medium) rs904628713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5367297 97307 RMVar_ID_97307 Human_SNP_ID_625387213 m1A Human chr17 - 45316826 45316826 45316826 CGCCCCGGAGCAGTGGGGTCGGCGGCCAGGCCAGCGCAGTCCGACGTACCCCGTCCAACCCACTC CGCCCCGGAGCAGTGGGGTCGGCGGCCAGGCCGGCGCAGTCCGACGTACCCCGTCCAACCCACTC T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45316824..45317050 26863196 MeRIP-seq:(Medium) rs1468114410 Functional Loss SNV dbSNP153 33..33 33 - - - 97308 RMVar_ID_97308 Human_SNP_ID_625387281 m1A Human chr17 - 45317005 45317005 45317005 GGTCGGCGGCCGGCGGCGGGAGATCGCGGGCGAGCGGAGCGCAACACTCGCTTGGTTGGGGAGAT GGTCGGCGGCCGGCGGCGGGAGATCGCGGGCGGGCGGAGCGCAACACTCGCTTGGTTGGGGAGAT T C MAP3K14 Ensembl:ENSG00000006062 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45316905..45317024 26863196 MeRIP-seq:(Medium) rs924041742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828657,Human_Splice_Rec_1828741 97309 RMVar_ID_97309 Human_SNP_ID_625406888 m1A Human chr17 + 45397115 45397115 45397115 ATGGGGCAAGGGACCCGAAATGCACTCCCAACAGGCATGGCCTGGAGACCCTCAGCGAAGAGTCC ATGGGGCAAGGGACCCGAAATGCACTCCCAACGGGCATGGCCTGGAGACCCTCAGCGAAGAGTCC A G AC003070.1 Ensembl:ENSG00000267344 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45397113..45397386 26863196 MeRIP-seq:(Medium) rs1221976679 Functional Loss SNV dbSNP153 33..33 33 - - - 97310 RMVar_ID_97310 Human_SNP_ID_625409168 m1A Human chr17 - 45406040 45406037 45406040 ACCGGAGCCCGTGTACGCGAACATAGAGAGGCAGCCCCGGGCCACTTCACCGGGCGCCGCTGCAG ACCGGAGCCCGTGTACGCGAACATAGAGAGGC___CCCGGGCCACTTCACCGGGCGCCGCTGCAG GGCT G ARHGAP27 Ensembl:ENSG00000159314 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45405877..45406078 26863196 MeRIP-seq:(Medium) rs996193332 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4432668,Human_RBP_ID_9378393 Human_Splice_Rec_1828750,Human_Splice_Rec_1828780,Human_Splice_Rec_1828812,Human_Splice_Rec_1828848,Human_Splice_Rec_1828910,Human_Splice_Rec_1828950,Human_Splice_Rec_1828974,Human_Splice_Rec_1828996,Human_Splice_Rec_1829004 RMVar_hsa_circ_366659 97311 RMVar_ID_97311 Human_SNP_ID_625419586 m1A Human chr17 + 45449456 45449456 45449456 AGCCATCTGCCCATTCACCCACCTATCTACCTATCTACCTACCCATCCACCTACCCACCAAGCCA AGCCATCTGCCCATTCACCCACCTATCTACCTGTCTACCTACCCATCCACCTACCCACCAAGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45449196..45449584 26863196 MeRIP-seq:(Medium) rs1483241297 Functional Loss SNV dbSNP153 33..33 33 - - - 97312 RMVar_ID_97312 Human_SNP_ID_625419656 m1A Human chr17 - 45449726 45449726 45449726 GATGGGCAGGTAGGTAGGTGGATGGGTAGGTAAGTAGGTGAATGAGCAGGTGGCTAGGTGGATGG GATGGGCAGGTAGGTAGGTGGATGGGTAGGTAGGTAGGTGAATGAGCAGGTGGCTAGGTGGATGG T C PLEKHM1 Ensembl:ENSG00000225190 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45449685..45450269 26863196 MeRIP-seq:(Medium) rs28970384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184826,RMVar_hsa_circ_184825,RMVar_hsa_circ_82969,RMVar_hsa_circ_340468,RMVar_hsa_circ_329010 97313 RMVar_ID_97313 Human_SNP_ID_625419787 m1A Human chr17 - 45450129 45450129 45450129 GGTAGGTGAATGAGCAGGTGGCTAGGTGGATGAGCAGGCGGCTAGGTGGATGGGTAGGTAGGTAG GGTAGGTGAATGAGCAGGTGGCTAGGTGGATGGGCAGGCGGCTAGGTGGATGGGTAGGTAGGTAG T C PLEKHM1 Ensembl:ENSG00000225190 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45449677..45450269 26863196 MeRIP-seq:(Medium) rs1209215327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821493,Human_RBP_ID_8189693 RMVar_hsa_circ_184826,RMVar_hsa_circ_184825,RMVar_hsa_circ_82969,RMVar_hsa_circ_340468,RMVar_hsa_circ_329010 97314 RMVar_ID_97314 Human_SNP_ID_625449045 m1A Human chr17 - 45585249 45585249 45585249 CTGCCCCCGACTCAATGCTCCCGCGCTCCCCCAAGCAGCCGCTGCGCCACCTCGCCCCGTCCCAG CTGCCCCCGACTCAATGCTCCCGCGCTCCCCCTAGCAGCCGCTGCGCCACCTCGCCCCGTCCCAG T A RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45585199..45585345 26863196 MeRIP-seq:(Medium) rs1432919678 Functional Loss SNV dbSNP153 33..33 33 - - - 97315 RMVar_ID_97315 Human_SNP_ID_625449046 m1A Human chr17 - 45585249 45585249 45585249 CTGCCCCCGACTCAATGCTCCCGCGCTCCCCCAAGCAGCCGCTGCGCCACCTCGCCCCGTCCCAG CTGCCCCCGACTCAATGCTCCCGCGCTCCCCCCAGCAGCCGCTGCGCCACCTCGCCCCGTCCCAG T G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45585199..45585345 26863196 MeRIP-seq:(Medium) rs1432919678 Functional Loss SNV dbSNP153 33..33 33 - - - 97316 RMVar_ID_97316 Human_SNP_ID_625458739 m1A Human chr17 - 45620497 45620497 45620497 CCCCGGGCCCCGCGGCCCCCCGCCTCCCAGCCAGGCCGCTCCCTCGAGCTCGTCGGGTCAGGGAC CCCCGGGCCCCGCGGCCCCCCGCCTCCCAGCCGGGCCGCTCCCTCGAGCTCGTCGGGTCAGGGAC T C RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45620435..45620565 26863196 MeRIP-seq:(Medium) rs2693382 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12869 97317 RMVar_ID_97317 Human_SNP_ID_625461793 m1A Human chr17 + 45634150 45634150 45634150 GCGGAGACCAGAAGGCTGGGAGGAAGGGAGCCACACGATTCTAGGAACAGCATGGGAGCCAGTGC GCGGAGACCAGAAGGCTGGGAGGAAGGGAGCCGCACGATTCTAGGAACAGCATGGGAGCCAGTGC A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45634108..45634299 26863196 MeRIP-seq:(Medium) rs1173306082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3548580,Human_RBP_ID_6601357,Human_RBP_ID_13032991 97318 RMVar_ID_97318 Human_SNP_ID_625461797 m1A Human chr17 + 45634169 45634169 45634169 GAGGAAGGGAGCCACACGATTCTAGGAACAGCATGGGAGCCAGTGCAGCTGGAACAGAATGAGCA GAGGAAGGGAGCCACACGATTCTAGGAACAGCGTGGGAGCCAGTGCAGCTGGAACAGAATGAGCA A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45634119..45634288 26863196 MeRIP-seq:(Medium) rs957594338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3548580,Human_RBP_ID_6601357,Human_RBP_ID_13032994,Human_RBP_ID_18531196 97319 RMVar_ID_97319 Human_SNP_ID_625502201 m1A Human chr17 - 45807015 45807015 45807015 GAGGCAGAGACGGGGTTCAGCCCCAGAAGGAGAAGGGCCTGCAGGCACAGGAGGCGAAGGACACA GAGGCAGAGACGGGGTTCAGCCCCAGAAGGAGCAGGGCCTGCAGGCACAGGAGGCGAAGGACACA T G MAPT-AS1 Ensembl:ENSG00000264589 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:45806950..45807035 26863410 MeRIP-seq:(Medium) rs1568043629 Functional Loss SNV dbSNP153 33..33 33 - - - 97320 RMVar_ID_97320 Human_SNP_ID_625524727 m1A Human chr17 + 45894610 45894610 45894610 CGGCACCAACAGCAGCGCCGCTGCCACCGCCCACCTTCTGCCGCCGCCACCACAGCCACCTTCTC CGGCACCAACAGCAGCGCCGCTGCCACCGCCCGCCTTCTGCCGCCGCCACCACAGCCACCTTCTC A G MAPT Ensembl:ENSG00000186868 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45894561..45894677 26863196 MeRIP-seq:(Medium) rs1321142871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1829585,Human_Splice_Rec_1829611,Human_Splice_Rec_1829633,Human_Splice_Rec_1829661,Human_Splice_Rec_1829681,Human_Splice_Rec_1829701,Human_Splice_Rec_1829709,Human_Splice_Rec_1829721,Human_Splice_Rec_1829737 97321 RMVar_ID_97321 Human_SNP_ID_625556885 m1A Human chr17 + 46024085 46024085 46024085 CGTCTCCACGGCATCTCAGCAATGTCTCCTCCACCGGCAGCATCGACATGGTAGACTCGCCCCAG CGTCTCCACGGCATCTCAGCAATGTCTCCTCCGCCGGCAGCATCGACATGGTAGACTCGCCCCAG A G MAPT Ensembl:ENSG00000186868 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:46023970..46024099 26863196 MeRIP-seq:(Medium) rs780581192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267428,RMVar_hsa_circ_265713 97322 RMVar_ID_97322 Human_SNP_ID_625557088 m1A Human chr17 - 46024761 46024759 46024761 TGTCTACTCTCCAGCACGTGGCTTCCTCTCCCACTCCCACTTCTTGTGCTTCCTCTCCCCTCTGC TGTCTACTCTCCAGCACGTGGCTTCCTCTCCC__TCCCACTTCTTGTGCTTCCTCTCCCCTCTGC AGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:46024711..46024812 26863196 MeRIP-seq:(Medium) rs1266936800 Functional Loss DEL dbSNP153 33..34 33 - - - 97323 RMVar_ID_97323 Human_SNP_ID_625557089 m1A Human chr17 - 46024761 46024761 46024761 TGTCTACTCTCCAGCACGTGGCTTCCTCTCCCACTCCCACTTCTTGTGCTTCCTCTCCCCTCTGC TGTCTACTCTCCAGCACGTGGCTTCCTCTCCCGCTCCCACTTCTTGTGCTTCCTCTCCCCTCTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:46024711..46024812 26863196 MeRIP-seq:(Medium) rs1309690946 Functional Loss SNV dbSNP153 33..33 33 - - - 97324 RMVar_ID_97324 Human_SNP_ID_625559496 m1A Human chr17 - 46033132 46033130 46033132 CCGCCCTGCATGCCAAATGTGAGGAGATGGAGAGGGCACGGTGGCTGTGGACCACGAGTGTGCCA CCGCCCTGCATGCCAAATGTGAGGAGATGGAG__GGCACGGTGGCTGTGGACCACGAGTGTGCCA CCT C KANSL1 Ensembl:ENSG00000120071 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:46033028..46033143 26863196 MeRIP-seq:(Medium) rs281865471 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3950764,Human_RBP_ID_5144221,Human_RBP_ID_6601727,Human_RBP_ID_9346039,Human_RBP_ID_13034232,Human_RBP_ID_18988676,Human_RBP_ID_22959606 Human_Splice_Rec_1829886,Human_Splice_Rec_1829887,Human_Splice_Rec_1829914,Human_Splice_Rec_1829915,Human_Splice_Rec_1829942,Human_Splice_Rec_1829943,Human_Splice_Rec_1829972,Human_Splice_Rec_1829973,Human_Splice_Rec_1829998,Human_Splice_Rec_1829999,Human_Splice_Rec_1830026,Human_Splice_Rec_1830027,Human_Splice_Rec_1830038,Human_Splice_Rec_1830039,Human_Splice_Rec_1830066,Human_Splice_Rec_1830067,Human_Splice_Rec_1830096,Human_Splice_Rec_1830097,Human_Splice_Rec_1830102,Human_Splice_Rec_1830103,Human_Splice_Rec_1830114,Human_Splice_Rec_1830115,Human_Splice_Rec_1830118,Human_Splice_Rec_1830119,Human_Splice_Rec_1830128,Human_Splice_Rec_1830129,Human_Splice_Rec_1830136,Human_Splice_Rec_1830137,Human_Splice_Rec_1830158,Human_Splice_Rec_1830159,Human_Splice_Rec_1830166,Human_Splice_Rec_1830167,Human_Splice_Rec_1830172,Human_Splice_Rec_1830173,Human_Splice_Rec_1830178,Human_Splice_Rec_1830202,Human_Splice_Rec_1830208 Clinvar_Rec_588 RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832 97325 RMVar_ID_97325 Human_SNP_ID_625568391 m1A Human chr17 - 46064508 46064508 46064508 TGCAGACATTGGTGAGCAGTTTTGGTAGAGGGAGAAAGGTGAATTAAAGCATGGTTGGAGTGGTT TGCAGACATTGGTGAGCAGTTTTGGTAGAGGGGGAAAGGTGAATTAAAGCATGGTTGGAGTGGTT T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:46064498..46064814 26863196 MeRIP-seq:(Medium) rs1227071516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81639,RMVar_hsa_circ_184831,RMVar_hsa_circ_119848,RMVar_hsa_circ_378857,RMVar_hsa_circ_123012,RMVar_hsa_circ_91644,RMVar_hsa_circ_103125,RMVar_hsa_circ_184835,RMVar_hsa_circ_184837,RMVar_hsa_circ_184838,RMVar_hsa_circ_184839,RMVar_hsa_circ_184836 97326 RMVar_ID_97326 Human_SNP_ID_625592396 m1A Human chr17 + 46151386 46151386 46151386 TCTTCCTCAAGATCTTCACAGGTCTTGCTCACACACTTCATACAGATCTCATTCAAACTGTCACC TCTTCCTCAAGATCTTCACAGGTCTTGCTCACGCACTTCATACAGATCTCATTCAAACTGTCACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:46151382..46151508 26863196 MeRIP-seq:(Medium) rs974725504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333316,RMVar_hsa_circ_358328,RMVar_hsa_circ_274873,RMVar_hsa_circ_341728 97327 RMVar_ID_97327 Human_SNP_ID_625595841 m1A Human chr17 - 46163823 46163823 46163823 GGGATATGTTGAAGACATAGTATTATAGGTACAGATGGTAAATGTAATGTGAGAAGAAAAAGAGA GGGATATGTTGAAGACATAGTATTATAGGTACGGATGGTAAATGTAATGTGAGAAGAAAAAGAGA T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:46163773..46163861 26863196 MeRIP-seq:(Medium) rs533146845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2509443,Human_RBP_ID_9863895,Human_RBP_ID_13038667 Human_miRNA_ID_2022746,Human_miRNA_ID_2022747,Human_miRNA_ID_2022748,Human_miRNA_ID_2022749,Human_miRNA_ID_2022750,Human_miRNA_ID_2261286,Human_miRNA_ID_2261287,Human_miRNA_ID_2261288,Human_miRNA_ID_2261289,Human_miRNA_ID_2261290,Human_miRNA_ID_2264334,Human_miRNA_ID_2264335,Human_miRNA_ID_2264336,Human_miRNA_ID_2264337,Human_miRNA_ID_2264338,Human_miRNA_ID_2267400,Human_miRNA_ID_2267401,Human_miRNA_ID_2267402,Human_miRNA_ID_2267403,Human_miRNA_ID_2267404,Human_miRNA_ID_2417636,Human_miRNA_ID_2417637,Human_miRNA_ID_2417638,Human_miRNA_ID_2417639,Human_miRNA_ID_2417640 RMVar_hsa_circ_123012,RMVar_hsa_circ_71139,RMVar_hsa_circ_184843,RMVar_hsa_circ_184839,RMVar_hsa_circ_117725,RMVar_hsa_circ_126756,RMVar_hsa_circ_94409,RMVar_hsa_circ_123231,RMVar_hsa_circ_184846,RMVar_hsa_circ_109764,RMVar_hsa_circ_184847,RMVar_hsa_circ_184848,RMVar_hsa_circ_184849,RMVar_hsa_circ_325152 97328 RMVar_ID_97328 Human_SNP_ID_625604907 m1A Human chr17 + 46193044 46193044 46193044 AGGCAGAGGGGGAGGGGAAGGCGGCGGCGGGGAGCGGCTGCTTTTTCTTCTCTTTCGGGCCCTTT AGGCAGAGGGGGAGGGGAAGGCGGCGGCGGGGGGCGGCTGCTTTTTCTTCTCTTTCGGGCCCTTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:46192875..46193137 26863196 MeRIP-seq:(Medium) rs1395131618 Functional Loss SNV dbSNP153 33..33 33 - - - 97329 RMVar_ID_97329 Human_SNP_ID_625605005 m1A Human chr17 + 46193251 46193251 46193251 ACCCAGGCCGCCACCCCCGGCCGCCTCTTTCCAGCCGGGGAGCGCGCTTCAGCCGCCCCCCGCGC ACCCAGGCCGCCACCCCCGGCCGCCTCTTTCCGGCCGGGGAGCGCGCTTCAGCCGCCCCCCGCGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:46193206..46193354 26863196 MeRIP-seq:(Medium) rs1321269964 Functional Loss SNV dbSNP153 33..33 33 - - - 97330 RMVar_ID_97330 Human_SNP_ID_625694318 m1A Human chr17 + 46763054 46763054 46763054 TGAGATGTGTATCTTTAGCAGGGCTTGTGGCCAGCAGATTTAGAAGTGAAGGCGGGCTCCTGGAC TGAGATGTGTATCTTTAGCAGGGCTTGTGGCCGGCAGATTTAGAAGTGAAGGCGGGCTCCTGGAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:46763003..46763402 32194978 MeRIP-seq:(Medium) rs1224402153 Functional Loss SNV dbSNP153 33..33 33 - - - 97331 RMVar_ID_97331 Human_SNP_ID_625695803 m1A Human chr17 - 46768588 46768588 46768588 GGAGACCCTCCGGGCCAAGTACTCGCTCTTCAAGCCACCCACGGAGAGGGACCTGGTCTACTACG GGAGACCCTCCGGGCCAAGTACTCGCTCTTCAGGCCACCCACGGAGAGGGACCTGGTCTACTACG T C WNT3 Ensembl:ENSG00000108379 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:46768537..46768643 26863196 MeRIP-seq:(Medium) rs886053073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27453512 Clinvar_Rec_589 RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846 97332 RMVar_ID_97332 Human_SNP_ID_625735019 m1A Human chr17 + 46923209 46923209 46923209 CTGCGGGGCCGGCGACATGGATCCCCTGTTCCAGCAAACGCACAAGTGAGGGCCGGTCGGGGAGC CTGCGGGGCCGGCGACATGGATCCCCTGTTCCGGCAAACGCACAAGTGAGGGCCGGTCGGGGAGC A G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:46923159..46923285 26863196 MeRIP-seq:(Medium) rs749270151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535572,Human_RBP_ID_4433376,Human_RBP_ID_9378397,Human_RBP_ID_18419634,Human_RBP_ID_18700277 Human_Splice_Rec_1830763,Human_Splice_Rec_1830771,Human_Splice_Rec_1830785,Human_Splice_Rec_1830793,Human_Splice_Rec_1830807,Human_Splice_Rec_1830817,Human_Splice_Rec_1830829,Human_Splice_Rec_1830831,Human_Splice_Rec_1830839,Human_Splice_Rec_1830849,Human_Splice_Rec_1830861,Human_Splice_Rec_1830873,Human_Splice_Rec_1830885,Human_Splice_Rec_1830889,Human_Splice_Rec_1830897,Human_Splice_Rec_1830905,Human_Splice_Rec_1830919,Human_Splice_Rec_1830929,Human_Splice_Rec_1830939,Human_Splice_Rec_1830945,Human_Splice_Rec_1830969,Human_Splice_Rec_1830985,Human_Splice_Rec_1830995,Human_Splice_Rec_1831005,Human_Splice_Rec_1831017,Human_Splice_Rec_1831033,Human_Splice_Rec_1831039,Human_Splice_Rec_1831047,Human_Splice_Rec_1831065,Human_Splice_Rec_1831083,Human_Splice_Rec_1831103,Human_Splice_Rec_1831111,Human_Splice_Rec_1831129,Human_Splice_Rec_1831139,Human_Splice_Rec_1831147,Human_Splice_Rec_1831197,Human_Splice_Rec_1831215 97333 RMVar_ID_97333 Human_SNP_ID_625735025 m1A Human chr17 + 46923220 46923220 46923220 GCGACATGGATCCCCTGTTCCAGCAAACGCACAAGTGAGGGCCGGTCGGGGAGCGGGCAGGGGCT GCGACATGGATCCCCTGTTCCAGCAAACGCACGAGTGAGGGCCGGTCGGGGAGCGGGCAGGGGCT A G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr17:46923193..46923332;chr17:46923176..46923225 26863196,32194978 MeRIP-seq:(Medium) rs1278419518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465484,Human_RBP_ID_6603844,Human_RBP_ID_9378397,Human_RBP_ID_18419634,Human_RBP_ID_23730589 Human_Splice_Rec_1830763,Human_Splice_Rec_1830771,Human_Splice_Rec_1830785,Human_Splice_Rec_1830793,Human_Splice_Rec_1830807,Human_Splice_Rec_1830817,Human_Splice_Rec_1830829,Human_Splice_Rec_1830831,Human_Splice_Rec_1830839,Human_Splice_Rec_1830849,Human_Splice_Rec_1830861,Human_Splice_Rec_1830873,Human_Splice_Rec_1830885,Human_Splice_Rec_1830889,Human_Splice_Rec_1830897,Human_Splice_Rec_1830905,Human_Splice_Rec_1830919,Human_Splice_Rec_1830929,Human_Splice_Rec_1830939,Human_Splice_Rec_1830945,Human_Splice_Rec_1830969,Human_Splice_Rec_1830985,Human_Splice_Rec_1830995,Human_Splice_Rec_1831005,Human_Splice_Rec_1831017,Human_Splice_Rec_1831033,Human_Splice_Rec_1831039,Human_Splice_Rec_1831047,Human_Splice_Rec_1831065,Human_Splice_Rec_1831083,Human_Splice_Rec_1831103,Human_Splice_Rec_1831111,Human_Splice_Rec_1831129,Human_Splice_Rec_1831139,Human_Splice_Rec_1831147,Human_Splice_Rec_1831197,Human_Splice_Rec_1831215 97334 RMVar_ID_97334 Human_SNP_ID_625741205 m1A Human chr17 + 46947003 46947002 46947003 TGCAACTGACTGCTGCCCCTGGGGAAGGTGGGACGGGGGCCAGATTCACAGGGGAGCCATGTGAG TGCAACTGACTGCTGCCCCTGGGGAAGGTGGG_CGGGGGCCAGATTCACAGGGGAGCCATGTGAG GA G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:46946952..46947123 26863196 MeRIP-seq:(Medium) rs1233794999 Functional Loss DEL dbSNP153 33..33 33 - - - 97335 RMVar_ID_97335 Human_SNP_ID_625741217 m1A Human chr17 - 46947053 46947053 46947053 TCCCTACTCTTTCCACAATCCACTCCAAACCCAGCCTGCTGAGAACCAAGCTCACATGGCTCCCC TCCCTACTCTTTCCACAATCCACTCCAAACCCGGCCTGCTGAGAACCAAGCTCACATGGCTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:46946871..46947274 26863196 MeRIP-seq:(Medium) rs1029825355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846 97336 RMVar_ID_97336 Human_SNP_ID_625758859 m1A Human chr17 - 47020062 47020062 47020062 TAAAGAGGGTGAAGCAAAAATGGGAGGAGAGCAGCGGTTAAGCAATGATGTGATGGGGCTAAATA TAAAGAGGGTGAAGCAAAAATGGGAGGAGAGCCGCGGTTAAGCAATGATGTGATGGGGCTAAATA T G AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47019972..47020080 26863196 MeRIP-seq:(Medium) rs1568269040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846 97337 RMVar_ID_97337 Human_SNP_ID_625767019 m1A Human chr17 + 47056384 47056384 47056384 TGGCAGCTGCTAGGGGTCTACAGGCGTGTACCACCATGCCCAGCTACAATTCTTATTATTCCCAA TGGCAGCTGCTAGGGGTCTACAGGCGTGTACCCCCATGCCCAGCTACAATTCTTATTATTCCCAA A C lnc-GOSR2-2 RNACentral:URS00008BCD23 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47056335..47056435 26863196 MeRIP-seq:(Medium) rs1423406549 Functional Loss SNV dbSNP153 33..33 33 - - - 97338 RMVar_ID_97338 Human_SNP_ID_625770198 m1A Human chr17 - 47068576 47068576 47068576 AAAATCAGAAAAAAACAAAAGAGATGGACGGCAGTGCGTGCGCAGGGGCAGTACCCATGCCGTTG AAAATCAGAAAAAAACAAAAGAGATGGACGGCCGTGCGTGCGCAGGGGCAGTACCCATGCCGTTG T G AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47068551..47068670 26863196 MeRIP-seq:(Medium) rs1027627922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846,RMVar_hsa_circ_184889,RMVar_hsa_circ_104255 97339 RMVar_ID_97339 Human_SNP_ID_625770768 m1A Human chr17 - 47071559 47071559 47071559 CAGGTCAAGGAAGTTCCTGAGGTCCCAGGGCTAATAAGTGGCCTGACTCCACCACCAGCCCCCAG CAGGTCAAGGAAGTTCCTGAGGTCCCAGGGCTGATAAGTGGCCTGACTCCACCACCAGCCCCCAG T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47071552..47071681 32194978 MeRIP-seq:(Medium) rs552652915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1831492,Human_Splice_Rec_1831496 RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846,RMVar_hsa_circ_184889,RMVar_hsa_circ_104255 97340 RMVar_ID_97340 Human_SNP_ID_625781572 m1A Human chr17 - 47118824 47118824 47118824 CCGCCCAAGCTTGGCCTATTTTATTTTTCCTCATACCTACTTTCAAAGTCATTTAGGTATTTGAA CCGCCCAAGCTTGGCCTATTTTATTTTTCCTCGTACCTACTTTCAAAGTCATTTAGGTATTTGAA T C CDC27 Ensembl:ENSG00000004897 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1713494 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_6604405,Human_RBP_ID_8090275,Human_RBP_ID_8818842,Human_RBP_ID_13044423,Human_RBP_ID_17005028,Human_RBP_ID_17260198,Human_RBP_ID_17376032,Human_RBP_ID_17491761,Human_RBP_ID_17894221,Human_RBP_ID_18293066,Human_RBP_ID_24415410,Human_RBP_ID_27665957 Human_miRNA_ID_1406818,Human_miRNA_ID_2749686 GWAS_ID_12870,GWAS_ID_12871,GWAS_ID_12872,GWAS_ID_12873,GWAS_ID_12874,GWAS_ID_12875,GWAS_ID_12876,GWAS_ID_12877,GWAS_ID_12878,GWAS_ID_12879,GWAS_ID_12880,GWAS_ID_12881,GWAS_ID_12882,GWAS_ID_12883,GWAS_ID_12884,GWAS_ID_12885,GWAS_ID_12886,GWAS_ID_12887,GWAS_ID_12888,GWAS_ID_12889,GWAS_ID_12890,GWAS_ID_12891,GWAS_ID_12892,GWAS_ID_12893,GWAS_ID_12894,GWAS_ID_12895,GWAS_ID_12896,GWAS_ID_12897,GWAS_ID_12898,GWAS_ID_12899,GWAS_ID_12900,GWAS_ID_12901,GWAS_ID_12902,GWAS_ID_12903,GWAS_ID_12904,GWAS_ID_12905,GWAS_ID_12906,GWAS_ID_12907,GWAS_ID_12908,GWAS_ID_12909,GWAS_ID_12910,GWAS_ID_12911,GWAS_ID_12912,GWAS_ID_12913,GWAS_ID_12914,GWAS_ID_12915,GWAS_ID_12916,GWAS_ID_12917,GWAS_ID_12918,GWAS_ID_12919,GWAS_ID_12920,GWAS_ID_12921,GWAS_ID_12922,GWAS_ID_12923,GWAS_ID_12924,GWAS_ID_12925,GWAS_ID_12926,GWAS_ID_12927,GWAS_ID_12928,GWAS_ID_12929,GWAS_ID_12930,GWAS_ID_12931,GWAS_ID_12932,GWAS_ID_12933,GWAS_ID_12934,GWAS_ID_12935,GWAS_ID_12936,GWAS_ID_12937,GWAS_ID_12938,GWAS_ID_12939 RMVar_hsa_circ_126162,RMVar_hsa_circ_184890 97341 RMVar_ID_97341 Human_SNP_ID_625798867 m1A Human chr17 - 47189217 47189217 47189217 TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACAGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACTGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC T A CDC27 Ensembl:ENSG00000004897 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:47189143..47189275;chr17:47189125..47189237 26863196 MeRIP-seq:(Medium) rs79580708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235478,Human_RBP_ID_491808,Human_RBP_ID_764181,Human_RBP_ID_819124,Human_RBP_ID_4433611,Human_RBP_ID_18420593,Human_RBP_ID_26333484 Human_Splice_Rec_1831501,Human_Splice_Rec_1831537,Human_Splice_Rec_1831577,Human_Splice_Rec_1831621,Human_Splice_Rec_1831657,Human_Splice_Rec_1831687,Human_Splice_Rec_1831747,Human_Splice_Rec_1831759,Human_Splice_Rec_1831789 RMVar_hsa_circ_121510,RMVar_hsa_circ_184903 97342 RMVar_ID_97342 Human_SNP_ID_625798868 m1A Human chr17 - 47189217 47189217 47189217 TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACAGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACGGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC T C CDC27 Ensembl:ENSG00000004897 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:47189143..47189275;chr17:47189125..47189237 26863196 MeRIP-seq:(Medium) rs79580708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235478,Human_RBP_ID_491808,Human_RBP_ID_764181,Human_RBP_ID_819124,Human_RBP_ID_4433611,Human_RBP_ID_18420593,Human_RBP_ID_26333484 Human_Splice_Rec_1831501,Human_Splice_Rec_1831537,Human_Splice_Rec_1831577,Human_Splice_Rec_1831621,Human_Splice_Rec_1831657,Human_Splice_Rec_1831687,Human_Splice_Rec_1831747,Human_Splice_Rec_1831759,Human_Splice_Rec_1831789 RMVar_hsa_circ_121510,RMVar_hsa_circ_184903 97343 RMVar_ID_97343 Human_SNP_ID_625798869 m1A Human chr17 - 47189217 47189217 47189217 TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACAGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACCGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC T G CDC27 Ensembl:ENSG00000004897 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:47189143..47189275;chr17:47189125..47189237 26863196 MeRIP-seq:(Medium) rs79580708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235478,Human_RBP_ID_491808,Human_RBP_ID_764181,Human_RBP_ID_819124,Human_RBP_ID_4433611,Human_RBP_ID_18420593,Human_RBP_ID_26333484 Human_Splice_Rec_1831501,Human_Splice_Rec_1831537,Human_Splice_Rec_1831577,Human_Splice_Rec_1831621,Human_Splice_Rec_1831657,Human_Splice_Rec_1831687,Human_Splice_Rec_1831747,Human_Splice_Rec_1831759,Human_Splice_Rec_1831789 RMVar_hsa_circ_121510,RMVar_hsa_circ_184903 97344 RMVar_ID_97344 Human_SNP_ID_625798872 m1A Human chr17 - 47189219 47189219 47189219 AATGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACAGGGGGGGCCTGAGGCACTGCAGAAAGTGGG AATGAGCAGGGGCTGGCCGGGCCGGAGCCGCTGCAGGGGGGGCCTGAGGCACTGCAGAAAGTGGG T C CDC27 Ensembl:ENSG00000004897 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47189132..47189250 26863196 MeRIP-seq:(Medium) rs11570448 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_235478,Human_RBP_ID_764181,Human_RBP_ID_819124,Human_RBP_ID_4465487,Human_RBP_ID_18420593,Human_RBP_ID_25293178,Human_RBP_ID_26333484 Human_Splice_Rec_1831501,Human_Splice_Rec_1831537,Human_Splice_Rec_1831577,Human_Splice_Rec_1831621,Human_Splice_Rec_1831657,Human_Splice_Rec_1831687,Human_Splice_Rec_1831747,Human_Splice_Rec_1831759,Human_Splice_Rec_1831789 RMVar_hsa_circ_121510,RMVar_hsa_circ_184903 97345 RMVar_ID_97345 Human_SNP_ID_625798873 m1A Human chr17 + 47189220 47189220 47189220 CCACTTTCTGCAGTGCCTCAGGCCCCCCCTGTAGCGGCTCCGGCCCGGCCAGCCCCTGCTCATTT CCACTTTCTGCAGTGCCTCAGGCCCCCCCTGTGGCGGCTCCGGCCCGGCCAGCCCCTGCTCATTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47189120..47189233 26863196 MeRIP-seq:(Medium) rs1416954543 Functional Loss SNV dbSNP153 33..33 33 - - - 97346 RMVar_ID_97346 Human_SNP_ID_625814540 m1A Human chr17 + 47254370 47254370 47254370 GTTCCCGCGCCTTGGCAGAGGGATGCCGCTGTAGCTTCCTGGGTGAGAGCGTGCGCGCGCGCGGG GTTCCCGCGCCTTGGCAGAGGGATGCCGCTGTCGCTTCCTGGGTGAGAGCGTGCGCGCGCGCGGG A C ITGB3,AC068234.1 Ensembl:ENSG00000259207,Ensembl:ENSG00000259753 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47254254..47254370 32194978 MeRIP-seq:(Medium) rs1372725264 Functional Loss SNV dbSNP153 33..33 33 - - - 97347 RMVar_ID_97347 Human_SNP_ID_625826719 m1A Human chr17 - 47307473 47307473 47307473 CAGGACCACCAGGATGTCAGGGCCCTTGGGACACTCTGTGAGGAAGAAGCACAGAGCAGGGCGGT CAGGACCACCAGGATGTCAGGGCCCTTGGGACGCTCTGTGAGGAAGAAGCACAGAGCAGGGCGGT T C AC068234.2 Ensembl:ENSG00000263293 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:47307451..47307537 32194978 MeRIP-seq:(Medium) rs1436328407 Functional Loss SNV dbSNP153 33..33 33 - - - 97348 RMVar_ID_97348 Human_SNP_ID_625830370 m1A Human chr17 + 47323634 47323634 47323634 AGGGAAGAGTGGCGAGCGGGTGGCAAGGACGGAGGGCGGAATCCCGGCCGGGGCTGCGGGAGGAA AGGGAAGAGTGGCGAGCGGGTGGCAAGGACGGCGGGCGGAATCCCGGCCGGGGCTGCGGGAGGAA A C EFCAB13,AC068234.1 Ensembl:ENSG00000178852,Ensembl:ENSG00000259753 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47323488..47323871 26863196 MeRIP-seq:(Medium) rs1466241737 Functional Loss SNV dbSNP153 33..33 33 - - - 97349 RMVar_ID_97349 Human_SNP_ID_625830539 m1A Human chr17 + 47324023 47324023 47324023 CAGCGCCGCCCGAGGGGCGGCAGGGGCTGACCACAGAGAGCGCGGGGGCCTCCAGCCGAGAGGAA CAGCGCCGCCCGAGGGGCGGCAGGGGCTGACCGCAGAGAGCGCGGGGGCCTCCAGCCGAGAGGAA A G EFCAB13,AC068234.1 Ensembl:ENSG00000178852,Ensembl:ENSG00000259753 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47323973..47324520 26863196 MeRIP-seq:(Medium) rs1042843014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1832009,Human_Splice_Rec_1832057,Human_Splice_Rec_1832065,Human_Splice_Rec_1832073 97350 RMVar_ID_97350 Human_SNP_ID_625830540 m1A Human chr17 + 47324023 47324023 47324023 CAGCGCCGCCCGAGGGGCGGCAGGGGCTGACCACAGAGAGCGCGGGGGCCTCCAGCCGAGAGGAA CAGCGCCGCCCGAGGGGCGGCAGGGGCTGACCTCAGAGAGCGCGGGGGCCTCCAGCCGAGAGGAA A T EFCAB13,AC068234.1 Ensembl:ENSG00000178852,Ensembl:ENSG00000259753 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47323973..47324520 26863196 MeRIP-seq:(Medium) rs1042843014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1832009,Human_Splice_Rec_1832057,Human_Splice_Rec_1832065,Human_Splice_Rec_1832073 97351 RMVar_ID_97351 Human_SNP_ID_625877939 m1A Human chr17 + 47531216 47531216 47531216 GCCCGCCAGTCCGCCCGCACCGCCTCCTTCCCAGCCCCTAGCGCTCCGGCTGGGTCTCTCCCCCG GCCCGCCAGTCCGCCCGCACCGCCTCCTTCCCTGCCCCTAGCGCTCCGGCTGGGTCTCTCCCCCG A T NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr17:47531115..47531275;chr17:47531165..47531325;chr17:47531151..47531334;chr17:47531125..47531270;chr17:47531133..47531287;chr17:47531162..47531289;chr17:47531170..47531270 26863196,32194978 MeRIP-seq:(Medium) rs1350946401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129603,Human_RBP_ID_17079632,Human_RBP_ID_17378405,Human_RBP_ID_18941798 RMVar_hsa_circ_184939,RMVar_hsa_circ_92997,RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 97352 RMVar_ID_97352 Human_SNP_ID_625877944 m1A Human chr17 - 47531228 47531224 47531229 GAGCCTGGGGGGCGGGGGAGAGACCCAGCCGGAGCGCTAGGGGCTGGGAAGGAGGCGGTGCGGGC GAGCCTGGGGGGCGGGGGAGAGACCCAGCCG_____CTAGGGGCTGGGAAGGAGGCGGTGCGGGC GCGCTC G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:47531091..47531341 26863410 MeRIP-seq:(Medium) rs1401521440 Functional Loss DEL dbSNP153 32..36 33 - - - 97353 RMVar_ID_97353 Human_SNP_ID_625878079 m1A Human chr17 + 47531485 47531485 47531485 CGAGCGGCTGCCTGCCGATGTCTCCCCCATCAACTACAGCCTTTGCCTCAAGCCCGACTTGCTGG CGAGCGGCTGCCTGCCGATGTCTCCCCCATCACCTACAGCCTTTGCCTCAAGCCCGACTTGCTGG A C NPEPPS Ensembl:ENSG00000141279 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:47531451..47531525 26863196 MeRIP-seq:(Medium) rs762187418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765437,Human_RBP_ID_904701,Human_RBP_ID_4474429 Human_Splice_Rec_1832206,Human_Splice_Rec_1832207,Human_Splice_Rec_1832240,Human_Splice_Rec_1832241,Human_Splice_Rec_1832250,Human_Splice_Rec_1832251,Human_Splice_Rec_1832296,Human_Splice_Rec_1832297,Human_Splice_Rec_1832308,Human_Splice_Rec_1832309,Human_Splice_Rec_1832319,Human_Splice_Rec_1832363,Human_Splice_Rec_1832369,Human_Splice_Rec_1832391 RMVar_hsa_circ_184939,RMVar_hsa_circ_92997,RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 97354 RMVar_ID_97354 Human_SNP_ID_625878080 m1A Human chr17 + 47531485 47531485 47531485 CGAGCGGCTGCCTGCCGATGTCTCCCCCATCAACTACAGCCTTTGCCTCAAGCCCGACTTGCTGG CGAGCGGCTGCCTGCCGATGTCTCCCCCATCAGCTACAGCCTTTGCCTCAAGCCCGACTTGCTGG A G NPEPPS Ensembl:ENSG00000141279 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:47531451..47531525 26863196 MeRIP-seq:(Medium) rs762187418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765437,Human_RBP_ID_904701,Human_RBP_ID_4474429 Human_Splice_Rec_1832206,Human_Splice_Rec_1832207,Human_Splice_Rec_1832240,Human_Splice_Rec_1832241,Human_Splice_Rec_1832250,Human_Splice_Rec_1832251,Human_Splice_Rec_1832296,Human_Splice_Rec_1832297,Human_Splice_Rec_1832308,Human_Splice_Rec_1832309,Human_Splice_Rec_1832319,Human_Splice_Rec_1832363,Human_Splice_Rec_1832369,Human_Splice_Rec_1832391 RMVar_hsa_circ_184939,RMVar_hsa_circ_92997,RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 97355 RMVar_ID_97355 Human_SNP_ID_625878082 m1A Human chr17 + 47531488 47531488 47531488 GCGGCTGCCTGCCGATGTCTCCCCCATCAACTACAGCCTTTGCCTCAAGCCCGACTTGCTGGACT GCGGCTGCCTGCCGATGTCTCCCCCATCAACTGCAGCCTTTGCCTCAAGCCCGACTTGCTGGACT A G NPEPPS Ensembl:ENSG00000141279 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:47531439..47531540 32194978 MeRIP-seq:(Medium) rs28482949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765437,Human_RBP_ID_904701 Human_Splice_Rec_1832206,Human_Splice_Rec_1832207,Human_Splice_Rec_1832240,Human_Splice_Rec_1832241,Human_Splice_Rec_1832250,Human_Splice_Rec_1832251,Human_Splice_Rec_1832296,Human_Splice_Rec_1832297,Human_Splice_Rec_1832308,Human_Splice_Rec_1832309,Human_Splice_Rec_1832319,Human_Splice_Rec_1832363,Human_Splice_Rec_1832369,Human_Splice_Rec_1832391 Human_miRNA_ID_2579951 RMVar_hsa_circ_184939,RMVar_hsa_circ_92997,RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 97356 RMVar_ID_97356 Human_SNP_ID_625895765 m1A Human chr17 + 47601695 47601695 47601695 CAACCAGGCCAAACTAAAAATTCTAATGGACAAGCCAGAGATGAATGTGGTTTTGAAAAATGTCA CAACCAGGCCAAACTAAAAATTCTAATGGACAGGCCAGAGATGAATGTGGTTTTGAAAAATGTCA A G NPEPPS Ensembl:ENSG00000141279 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:47601646..47601797 32194978 MeRIP-seq:(Medium) rs1392593867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491827,Human_RBP_ID_3950780,Human_RBP_ID_9072955,Human_RBP_ID_18439157,Human_RBP_ID_18988694,Human_RBP_ID_23731137,Human_RBP_ID_27666025 Human_Splice_Rec_1832278,Human_Splice_Rec_1832279,Human_Splice_Rec_1832346,Human_Splice_Rec_1832347,Human_Splice_Rec_1832464,Human_Splice_Rec_1832465,Human_Splice_Rec_1832508,Human_Splice_Rec_1832509 Human_miRNA_ID_240266,Human_miRNA_ID_655756,Human_miRNA_ID_955628,Human_miRNA_ID_2120558,Human_miRNA_ID_2123773,Human_miRNA_ID_2126994,Human_miRNA_ID_2130213,Human_miRNA_ID_2602836 RMVar_hsa_circ_73355,RMVar_hsa_circ_57789,RMVar_hsa_circ_18674,RMVar_hsa_circ_83658,RMVar_hsa_circ_63230,RMVar_hsa_circ_184949,RMVar_hsa_circ_10067,RMVar_hsa_circ_281434,RMVar_hsa_circ_71428,RMVar_hsa_circ_351877,RMVar_hsa_circ_303115,RMVar_hsa_circ_343398,RMVar_hsa_circ_300423,RMVar_hsa_circ_281733,RMVar_hsa_circ_184961,RMVar_hsa_circ_184963,RMVar_hsa_circ_19790,RMVar_hsa_circ_184962,RMVar_hsa_circ_184960,RMVar_hsa_circ_43407,RMVar_hsa_circ_331624,RMVar_hsa_circ_298544,RMVar_hsa_circ_306026,RMVar_hsa_circ_314393,RMVar_hsa_circ_326177,RMVar_hsa_circ_300211,RMVar_hsa_circ_98854,RMVar_hsa_circ_184964,RMVar_hsa_circ_184966,RMVar_hsa_circ_184967,RMVar_hsa_circ_184965,RMVar_hsa_circ_45870,RMVar_hsa_circ_314327,RMVar_hsa_circ_342818,RMVar_hsa_circ_312331,RMVar_hsa_circ_184971,RMVar_hsa_circ_184972,RMVar_hsa_circ_288854,RMVar_hsa_circ_184970,RMVar_hsa_circ_284235,RMVar_hsa_circ_184973,RMVar_hsa_circ_184975,RMVar_hsa_circ_184976,RMVar_hsa_circ_184974 97357 RMVar_ID_97357 Human_SNP_ID_625897412 m1A Human chr17 - 47608685 47608685 47608685 TTTGCTGTTTCTTCCTTTTCCACACAATCTCTAAATCCTGAACTCAGACCACTTTCTTCTACTTA TTTGCTGTTTCTTCCTTTTCCACACAATCTCTCAATCCTGAACTCAGACCACTTTCTTCTACTTA T G AC025682.2 Ensembl:ENSG00000263766 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47608683..47608807 26863196 MeRIP-seq:(Medium) rs1431248971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184969 97358 RMVar_ID_97358 Human_SNP_ID_625906232 m1A Human chr17 - 47645094 47645094 47645094 TGGGAAGGAGCTTGGGGATTACAAGTTACTGCAAGAATGCCAGTGTCCCCAAAACAGAGAACAAG TGGGAAGGAGCTTGGGGATTACAAGTTACTGCCAGAATGCCAGTGTCCCCAAAACAGAGAACAAG T G AC025682.2 Ensembl:ENSG00000263766 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47645090..47645198 26863196 MeRIP-seq:(Medium) rs1189283256 Functional Loss SNV dbSNP153 33..33 33 - - - 97359 RMVar_ID_97359 Human_SNP_ID_625907419 m1A Human chr17 - 47649478 47649461 47649478 GTCGGGGCGCGGGAAGGCGGGAGGTGCCCGGCAACCCTAGGAGCCCGGCGCGGGGCACGATGGGA GTCGGGGCGCGGGAAGGCGGGAGGTGCCCGGC_________________GCGGGGCACGATGGGA CGCCGGGCTCCTAGGGTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47649429..47649593 26863196 MeRIP-seq:(Medium) rs1409906013 Functional Loss DEL dbSNP153 33..49 33 - - - Human_Splice_Rec_1832537,Human_Splice_Rec_1832545,Human_Splice_Rec_1832551 97360 RMVar_ID_97360 Human_SNP_ID_625907705 m1A Human chr17 + 47650008 47650008 47650008 TCCCGAGCACCAGCGCGCTCTGAGCTGCCCCCAGGGTCCCTCCCCCGCCGCCAGCAGCCCATTTG TCCCGAGCACCAGCGCGCTCTGAGCTGCCCCCGGGGTCCCTCCCCCGCCGCCAGCAGCCCATTTG A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:47649870..47650175;chr17:47649976..47650175 26863196 MeRIP-seq:(Medium) rs896114418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47222,Human_RBP_ID_235802,Human_RBP_ID_491875,Human_RBP_ID_4474468,Human_RBP_ID_5441539,Human_RBP_ID_5497191,Human_RBP_ID_6605427,Human_RBP_ID_8253473,Human_RBP_ID_9326700,Human_RBP_ID_13048149,Human_RBP_ID_17260214,Human_RBP_ID_17378406,Human_RBP_ID_17494954,Human_RBP_ID_18700525,Human_RBP_ID_18943322,Human_RBP_ID_22443754,Human_RBP_ID_22532975,Human_RBP_ID_22952792,Human_RBP_ID_25293983,Human_RBP_ID_26963987 Human_miRNA_ID_2147204,Human_miRNA_ID_2352141,Human_miRNA_ID_2988633,Human_miRNA_ID_3022334,Human_miRNA_ID_3047687 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97361 RMVar_ID_97361 Human_SNP_ID_625907744 m1A Human chr17 + 47650081 47650081 47650081 AAGTAAGGGAAGAGGAGAGGAAGGGGAGCCGGACCGACTACCCAGACAGAGCCGGTGAATGGGTT AAGTAAGGGAAGAGGAGAGGAAGGGGAGCCGGGCCGACTACCCAGACAGAGCCGGTGAATGGGTT A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:47649825..47650175;chr17:47649844..47650175 26863196 MeRIP-seq:(Medium) rs899438086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47222,Human_RBP_ID_235803,Human_RBP_ID_821170,Human_RBP_ID_5319082,Human_RBP_ID_6605428,Human_RBP_ID_9341017,Human_RBP_ID_17080293,Human_RBP_ID_17669962,Human_RBP_ID_22445555 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97362 RMVar_ID_97362 Human_SNP_ID_625907748 m1A Human chr17 + 47650092 47650092 47650092 GAGGAGAGGAAGGGGAGCCGGACCGACTACCCAGACAGAGCCGGTGAATGGGTTTGTGGTGACCC GAGGAGAGGAAGGGGAGCCGGACCGACTACCCGGACAGAGCCGGTGAATGGGTTTGTGGTGACCC A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr17:47649992..47650267;chr17:47649851..47650300 26863196,26863410 MeRIP-seq:(Medium) rs994882954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821170,Human_RBP_ID_1535692,Human_RBP_ID_9340993,Human_RBP_ID_17669962,Human_RBP_ID_22445555 Human_miRNA_ID_3069931 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97363 RMVar_ID_97363 Human_SNP_ID_625907783 m1A Human chr17 + 47650157 47650155 47650157 CCGCCCCCCACCCCACCCTCCCTTCCCACCCGACCCCCAACCCCCATCCCCAGTTCGAGCCGCCG CCGCCCCCCACCCCACCCTCCCTTCCCACCC__CCCCCAACCCCCATCCCCAGTTCGAGCCGCCG CGA C KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:47649874..47650174 26863410 MeRIP-seq:(Medium) rs1242765828 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_47223,Human_RBP_ID_278307,Human_RBP_ID_5129604,Human_RBP_ID_5420169,Human_RBP_ID_5441543,Human_RBP_ID_5497192,Human_RBP_ID_9072966,Human_RBP_ID_18700529,Human_RBP_ID_18941800,Human_RBP_ID_23731191 Human_miRNA_ID_842852 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97364 RMVar_ID_97364 Human_SNP_ID_625907787 m1A Human chr17 + 47650157 47650157 47650157 CCGCCCCCCACCCCACCCTCCCTTCCCACCCGACCCCCAACCCCCATCCCCAGTTCGAGCCGCCG CCGCCCCCCACCCCACCCTCCCTTCCCACCCGCCCCCCAACCCCCATCCCCAGTTCGAGCCGCCG A C KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:47649874..47650174 26863410 MeRIP-seq:(Medium) rs1355887483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47223,Human_RBP_ID_278307,Human_RBP_ID_5129604,Human_RBP_ID_5420169,Human_RBP_ID_5441543,Human_RBP_ID_5497192,Human_RBP_ID_9072966,Human_RBP_ID_18700529,Human_RBP_ID_18941800,Human_RBP_ID_23731191 Human_miRNA_ID_842852 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97365 RMVar_ID_97365 Human_SNP_ID_625907802 m1A Human chr17 + 47650182 47650180 47650183 CCACCCGACCCCCAACCCCCATCCCCAGTTCGAGCCGCCGCCCGAAAGGCCGGGCCGTCGTCTTA CCACCCGACCCCCAACCCCCATCCCCAGTTC___CCGCCGCCCGAAAGGCCGGGCCGTCGTCTTA CGAG C KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:47650085..47650236 26863410 MeRIP-seq:(Medium) rs1441540522 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1368685,Human_RBP_ID_4433764,Human_RBP_ID_5129604,Human_RBP_ID_5420169,Human_RBP_ID_5441544,Human_RBP_ID_5497192,Human_RBP_ID_8824777,Human_RBP_ID_9072966,Human_RBP_ID_9257877,Human_RBP_ID_9290167,Human_RBP_ID_9326701,Human_RBP_ID_9376243,Human_RBP_ID_18700529,Human_RBP_ID_18941800,Human_RBP_ID_23731191,Human_RBP_ID_26963992 Human_Splice_Rec_1832596 RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986 97366 RMVar_ID_97366 Human_SNP_ID_625912841 m1A Human chr17 + 47668401 47668401 47668401 GAAGGACCAGAGCCCAGTCAGCTCAAACCACTAGTTATACAGGTGAAACTGAGGGATTTTTGGAG GAAGGACCAGAGCCCAGTCAGCTCAAACCACTGGTTATACAGGTGAAACTGAGGGATTTTTGGAG A G KPNB1 Ensembl:ENSG00000108424 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47668232..47668412 26863196 MeRIP-seq:(Medium) rs761912022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235811,Human_RBP_ID_764640,Human_RBP_ID_1287001,Human_RBP_ID_1860978,Human_RBP_ID_3526471,Human_RBP_ID_3950786,Human_RBP_ID_8818945,Human_RBP_ID_9376251,Human_RBP_ID_17260233,Human_RBP_ID_17376060,Human_RBP_ID_17491803,Human_RBP_ID_17904387,Human_RBP_ID_18988705,Human_RBP_ID_19083032,Human_RBP_ID_22952873,Human_RBP_ID_25294311,Human_RBP_ID_27453602,Human_RBP_ID_27666072 Human_Splice_Rec_1832571,Human_Splice_Rec_1832621,Human_Splice_Rec_1832679,Human_Splice_Rec_1832711,Human_Splice_Rec_1832735 Human_miRNA_ID_2058249,Human_miRNA_ID_2058250,Human_miRNA_ID_2058251 RMVar_hsa_circ_103109,RMVar_hsa_circ_81118,RMVar_hsa_circ_184986,RMVar_hsa_circ_124020,RMVar_hsa_circ_184987,RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_184988,RMVar_hsa_circ_353897,RMVar_hsa_circ_75680,RMVar_hsa_circ_125661,RMVar_hsa_circ_62822,RMVar_hsa_circ_110452,RMVar_hsa_circ_184992,RMVar_hsa_circ_184994,RMVar_hsa_circ_42980,RMVar_hsa_circ_184993,RMVar_hsa_circ_184991,RMVar_hsa_circ_376640,RMVar_hsa_circ_24523,RMVar_hsa_circ_76937,RMVar_hsa_circ_3055,RMVar_hsa_circ_111711,RMVar_hsa_circ_92241,RMVar_hsa_circ_109129,RMVar_hsa_circ_184996,RMVar_hsa_circ_184997,RMVar_hsa_circ_184995,RMVar_hsa_circ_185002,RMVar_hsa_circ_185001,RMVar_hsa_circ_296207,RMVar_hsa_circ_346472,RMVar_hsa_circ_185003,RMVar_hsa_circ_271528,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_291979,RMVar_hsa_circ_271546,RMVar_hsa_circ_99626,RMVar_hsa_circ_114740,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_185007,RMVar_hsa_circ_185009,RMVar_hsa_circ_185010,RMVar_hsa_circ_185008,RMVar_hsa_circ_185006,RMVar_hsa_circ_272955,RMVar_hsa_circ_281671,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,RMVar_hsa_circ_293090,RMVar_hsa_circ_273878,RMVar_hsa_circ_126447,RMVar_hsa_circ_125485,RMVar_hsa_circ_185014,RMVar_hsa_circ_78934,RMVar_hsa_circ_98680,RMVar_hsa_circ_89112,RMVar_hsa_circ_185018,RMVar_hsa_circ_185020,RMVar_hsa_circ_185022,RMVar_hsa_circ_185021,RMVar_hsa_circ_185019,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_98713,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_185025,RMVar_hsa_circ_93967,RMVar_hsa_circ_306463,RMVar_hsa_circ_370082,RMVar_hsa_circ_185026,RMVar_hsa_circ_185027,RMVar_hsa_circ_185028 97367 RMVar_ID_97367 Human_SNP_ID_625915392 m1A Human chr17 - 47678415 47678414 47678415 GAGCGGACGAAGGGAACTGGGTTGTATACTCAACGGTGTACGTTCTCCTGATCCCCCTTTAATCC GAGCGGACGAAGGGAACTGGGTTGTATACTCA_CGGTGTACGTTCTCCTGATCCCCCTTTAATCC GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47678401..47678425 32194978 MeRIP-seq:(Medium) rs1300839773 Functional Loss DEL dbSNP153 33..33 33 - - - 97368 RMVar_ID_97368 Human_SNP_ID_625919827 m1A Human chr17 + 47694391 47694391 47694391 TCCCCCTCCGCCGCCGTTCCTCAGGCCGCGCCACTCCCGGAGCCCCTTCCCCGGCCCCGAGAGGG TCCCCCTCCGCCGCCGTTCCTCAGGCCGCGCCGCTCCCGGAGCCCCTTCCCCGGCCCCGAGAGGG A G TBKBP1 Ensembl:ENSG00000198933 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47694368..47694538 26863196 MeRIP-seq:(Medium) rs1443685153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6866,Human_RBP_ID_3543011,Human_RBP_ID_8189705,Human_RBP_ID_22715750,Human_RBP_ID_26782372 97369 RMVar_ID_97369 Human_SNP_ID_625920457 m1A Human chr17 - 47696119 47696119 47696119 CGTCAGGATGCTGATGTCGTCCTCGAACATGGACTCCATGGTGAGGGCCGGGCCGCGGCCCACAC CGTCAGGATGCTGATGTCGTCCTCGAACATGGTCTCCATGGTGAGGGCCGGGCCGCGGCCCACAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47696083..47696171 26863196 MeRIP-seq:(Medium) rs1291181572 Functional Loss SNV dbSNP153 33..33 33 - - - 97370 RMVar_ID_97370 Human_SNP_ID_625923792 m1A Human chr17 + 47708355 47708355 47708355 AGTTCTTCCTCCACAGCTGGGACGGTAGACCCACTGCCCTTCTCGTCTTTCCCACTGCCCTCTGA AGTTCTTCCTCCACAGCTGGGACGGTAGACCCCCTGCCCTTCTCGTCTTTCCCACTGCCCTCTGA A C TBKBP1 Ensembl:ENSG00000198933 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47708343..47708436 26863196 MeRIP-seq:(Medium) rs575480057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22543424,Human_RBP_ID_22656488 97371 RMVar_ID_97371 Human_SNP_ID_625924022 m1A Human chr17 - 47708886 47708886 47708886 GACGGGCGACGGGCAGGAGGGTGAGGCCGGAGAGCGGCGCTGCTGCGGCGAGGGGCACGGGGGCA GACGGGCGACGGGCAGGAGGGTGAGGCCGGAGGGCGGCGCTGCTGCGGCGAGGGGCACGGGGGCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:47708751..47709125 26863410 MeRIP-seq:(Medium) rs1390209299 Functional Loss SNV dbSNP153 33..33 33 - - - 97372 RMVar_ID_97372 Human_SNP_ID_625948531 m1A Human chr17 - 47807642 47807642 47807642 TCCCTCCCGTCTCAGCTCAGCGGATCCCCCAGAGTGGAGGAGGCCTCTCCATGAGGAGGGGAGCA TCCCTCCCGTCTCAGCTCAGCGGATCCCCCAGGGTGGAGGAGGCCTCTCCATGAGGAGGGGAGCA T C OSBPL7 Ensembl:ENSG00000006025 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47807594..47807814 26863196 MeRIP-seq:(Medium) rs1180148514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492043,Human_RBP_ID_18988715 97373 RMVar_ID_97373 Human_SNP_ID_625948699 m1A Human chr17 + 47808387 47808387 47808387 TTGTTGGTCACCCACCACTCTTTCCCGCTGCTATCCGTCTGCCGCCTGGTGGGAGAAGGCGGTGG TTGTTGGTCACCCACCACTCTTTCCCGCTGCTGTCCGTCTGCCGCCTGGTGGGAGAAGGCGGTGG A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47808331..47808435 26863196 MeRIP-seq:(Medium) rs1206464711 Functional Loss SNV dbSNP153 33..33 33 - - - 97374 RMVar_ID_97374 Human_SNP_ID_625948768 m1A Human chr17 - 47808568 47808568 47808568 GCAGCGAGACAGGCGCAAAGTCATGGAGGAAAACAACATCGTACACCAGGCTCGCTTCTTCAGGT GCAGCGAGACAGGCGCAAAGTCATGGAGGAAAGCAACATCGTACACCAGGCTCGCTTCTTCAGGT T C OSBPL7 Ensembl:ENSG00000006025 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47808317..47808655 26863196 MeRIP-seq:(Medium) rs1475428826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6867,Human_RBP_ID_3952610 Human_Splice_Rec_1832870,Human_Splice_Rec_1832871,Human_Splice_Rec_1832890,Human_Splice_Rec_1832891,Human_Splice_Rec_1832934,Human_Splice_Rec_1832935,Human_Splice_Rec_1832976,Human_Splice_Rec_1832977,Human_Splice_Rec_1833004,Human_Splice_Rec_1833005,Human_Splice_Rec_1833010,Human_Splice_Rec_1833011 RMVar_hsa_circ_92090,RMVar_hsa_circ_185043 97375 RMVar_ID_97375 Human_SNP_ID_625949590 m1A Human chr17 + 47811305 47811305 47811305 CCACTTGGAATGGCTCCACATCTGGAGCCTTCAATTCCAACATCCCACAGCCTGCCTGCCTTGCC CCACTTGGAATGGCTCCACATCTGGAGCCTTCCATTCCAACATCCCACAGCCTGCCTGCCTTGCC A C RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47811262..47811516 26863196 MeRIP-seq:(Medium) rs1427792119 Functional Loss SNV dbSNP153 33..33 33 - - - 97376 RMVar_ID_97376 Human_SNP_ID_625950001 m1A Human chr17 + 47812895 47812895 47812895 AGGCCTCTTTCCCTTCACTGGCAGGGCTCCTCAGCATCTGGCCCACCTTGTCTTCCAGCCCCATC AGGCCTCTTTCCCTTCACTGGCAGGGCTCCTCCGCATCTGGCCCACCTTGTCTTCCAGCCCCATC A C RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47812844..47813046 26863196 MeRIP-seq:(Medium) rs890768134 Functional Loss SNV dbSNP153 33..33 33 - - - 97377 RMVar_ID_97377 Human_SNP_ID_625953175 m1A Human chr17 + 47824109 47824109 47824109 ATCATTACTAGTGAAAACCAAGTGACAAACACACTCCCCGACCCCAAGTTCTTCCACATGTCCCA ATCATTACTAGTGAAAACCAAGTGACAAACACGCTCCCCGACCCCAAGTTCTTCCACATGTCCCA A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47824058..47824325 26863196 MeRIP-seq:(Medium) rs1329409152 Functional Loss SNV dbSNP153 33..33 33 - - - 97378 RMVar_ID_97378 Human_SNP_ID_625954034 m1A Human chr17 - 47827141 47827141 47827141 AGATAGCAGCAGTTTTCCAGGACAACCGAATGATAGCCGTCTGCCAGAATGTGGCTCTGAGTGCA AGATAGCAGCAGTTTTCCAGGACAACCGAATGGTAGCCGTCTGCCAGAATGTGGCTCTGAGTGCA T C MRPL10 Ensembl:ENSG00000159111 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47827092..47828344 26863196 MeRIP-seq:(Medium) rs1209021436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535917,Human_RBP_ID_4434243,Human_RBP_ID_13050160,Human_RBP_ID_17905471,Human_RBP_ID_23731537,Human_RBP_ID_26452439,Human_RBP_ID_26813755 Human_Splice_Rec_1833062,Human_Splice_Rec_1833070,Human_Splice_Rec_1833080,Human_Splice_Rec_1833088,Human_Splice_Rec_1833096,Human_Splice_Rec_1833102 Human_miRNA_ID_1181483,Human_miRNA_ID_2010945,Human_miRNA_ID_2010946,Human_miRNA_ID_2565662,Human_miRNA_ID_2565663 RMVar_hsa_circ_98911,RMVar_hsa_circ_346449,RMVar_hsa_circ_185046,RMVar_hsa_circ_185047,RMVar_hsa_circ_98739,RMVar_hsa_circ_185048 97379 RMVar_ID_97379 Human_SNP_ID_625954044 m1A Human chr17 - 47827173 47827161 47827173 GGAGATAGGCCTCATCAGGCTTCTCCGCCGGGAGATAGCAGCAGTTTTCCAGGACAACCGAATGA GGAGATAGGCCTCATCAGGCTTCTCCGCCGGG____________TTTTCCAGGACAACCGAATGA ACTGCTGCTATCT A MRPL10 Ensembl:ENSG00000159111 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47827126..47827225 26863196 MeRIP-seq:(Medium) rs1567950303 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_4434244,Human_RBP_ID_6606020,Human_RBP_ID_17262965,Human_RBP_ID_17378420,Human_RBP_ID_22444717 Human_Splice_Rec_1833062,Human_Splice_Rec_1833070,Human_Splice_Rec_1833080,Human_Splice_Rec_1833088,Human_Splice_Rec_1833096,Human_Splice_Rec_1833102 RMVar_hsa_circ_98911,RMVar_hsa_circ_346449,RMVar_hsa_circ_185046,RMVar_hsa_circ_185047,RMVar_hsa_circ_98739,RMVar_hsa_circ_185048 97380 RMVar_ID_97380 Human_SNP_ID_625954486 m1A Human chr17 - 47828659 47828659 47828659 TGTTGCTATATGCCCTCCCAGGCCGGCTGCCTACCCTCCAGACTGTCCGCTATGGCTCCAAGGCT TGTTGCTATATGCCCTCCCAGGCCGGCTGCCTGCCCTCCAGACTGTCCGCTATGGCTCCAAGGCT T C MRPL10 Ensembl:ENSG00000159111 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47828551..47829206 32194978 MeRIP-seq:(Medium) rs1254265420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535918,Human_RBP_ID_4464632,Human_RBP_ID_5318435,Human_RBP_ID_22444718 Human_Splice_Rec_1833060,Human_Splice_Rec_1833068,Human_Splice_Rec_1833078,Human_Splice_Rec_1833086,Human_Splice_Rec_1833094,Human_Splice_Rec_1833100,Human_Splice_Rec_1833104 Human_miRNA_ID_2793613,Human_miRNA_ID_2793614 RMVar_hsa_circ_76812,RMVar_hsa_circ_98911,RMVar_hsa_circ_346449,RMVar_hsa_circ_185046,RMVar_hsa_circ_185047,RMVar_hsa_circ_98739,RMVar_hsa_circ_185048,RMVar_hsa_circ_185049 97381 RMVar_ID_97381 Human_SNP_ID_625954494 m1A Human chr17 - 47828672 47828672 47828672 TTGCCTCTAACCATGTTGCTATATGCCCTCCCAGGCCGGCTGCCTACCCTCCAGACTGTCCGCTA TTGCCTCTAACCATGTTGCTATATGCCCTCCCCGGCCGGCTGCCTACCCTCCAGACTGTCCGCTA T G MRPL10 Ensembl:ENSG00000159111 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:47828589..47829157 26863410 MeRIP-seq:(Medium) rs747919172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465491,Human_RBP_ID_5318435 RMVar_hsa_circ_98911,RMVar_hsa_circ_185047,RMVar_hsa_circ_98739,RMVar_hsa_circ_185048 97382 RMVar_ID_97382 Human_SNP_ID_625955153 m1A Human chr17 - 47831453 47831453 47831453 GCGAGGGGGTCTCCTGCCCCAGGCGGGTAAGGAGTGGCCCAGGTCCTCACGGCGTGTCTTGCGGC GCGAGGGGGTCTCCTGCCCCAGGCGGGTAAGGTGTGGCCCAGGTCCTCACGGCGTGTCTTGCGGC T A MRPL10 Ensembl:ENSG00000159111 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:47831451..47831500 32194978 MeRIP-seq:(Medium) rs373985626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19083054 97383 RMVar_ID_97383 Human_SNP_ID_625957167 m1A Human chr17 + 47838427 47838427 47838427 GCACCTGGGGGGCCTGGGCCACCCCCATCCCGAAGATGAAAGGTTTGAACACAGACCTAGAGGGG GCACCTGGGGGGCCTGGGCCACCCCCATCCCGCAGATGAAAGGTTTGAACACAGACCTAGAGGGG A C RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:47838376..47838545 26863196 MeRIP-seq:(Medium) rs924494537 Functional Loss SNV dbSNP153 33..33 33 - - - 97384 RMVar_ID_97384 Human_SNP_ID_625957560 m1A Human chr17 + 47839544 47839544 47839544 AGCAGGAAGGTGCTATGGTAGGAGAATGGCGCAGCATCCTCCAGGCAGTTGCCCCCCTGCCCATA AGCAGGAAGGTGCTATGGTAGGAGAATGGCGCGGCATCCTCCAGGCAGTTGCCCCCCTGCCCATA A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47839494..47839633 26863196 MeRIP-seq:(Medium) rs1301034009 Functional Loss SNV dbSNP153 33..33 33 - - - 97385 RMVar_ID_97385 Human_SNP_ID_625958042 m1A Human chr17 - 47841054 47841054 47841054 TCCGAAGGGCCGGGACTCCCAGTGGGGGCGGGACCCCCGGAGTGCCCGCCTGCGGACTCCCAAGC TCCGAAGGGCCGGGACTCCCAGTGGGGGCGGGCCCCCCGGAGTGCCCGCCTGCGGACTCCCAAGC T G SCRN2 Ensembl:ENSG00000141295 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47841047..47841242 26863196 MeRIP-seq:(Medium) rs981043486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9424057,Human_RBP_ID_22063191 RMVar_hsa_circ_185052 97386 RMVar_ID_97386 Human_SNP_ID_625958060 m1A Human chr17 - 47841108 47841108 47841108 CGCAGGGCCGCAGGACTCTTGGTGGGGTAGCGAGGGGGACGGTCCCACGACTGCTCCGAAGGGCC CGCAGGGCCGCAGGACTCTTGGTGGGGTAGCGGGGGGGACGGTCCCACGACTGCTCCGAAGGGCC T C SCRN2 Ensembl:ENSG00000141295 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47841099..47841275 26863196 MeRIP-seq:(Medium) rs368513514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5318436,Human_RBP_ID_5367357,Human_RBP_ID_9422914,Human_RBP_ID_22063191 97387 RMVar_ID_97387 Human_SNP_ID_625971580 m1A Human chr17 - 47895754 47895754 47895754 CCCTAAGTCCAGTCTCGCCCAGGTGTGGCAGGAGCTTTTACCTGCTCTTCGGCAGTAGCCGGCTG CCCTAAGTCCAGTCTCGCCCAGGTGTGGCAGGGGCTTTTACCTGCTCTTCGGCAGTAGCCGGCTG T C AC018521.5 Ensembl:ENSG00000264920 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47895675..47895755 26863196 MeRIP-seq:(Medium) rs985833240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465496 Human_Splice_Rec_1833269,Human_Splice_Rec_1833273 97388 RMVar_ID_97388 Human_SNP_ID_625971821 m1A Human chr17 + 47896347 47896347 47896347 CGGGGTCTTCCCGGCCCCCAAGGGTCAGGAAGACGGGCAGAGGCCGCGGGGAGAGGGAGCCGAGG CGGGGTCTTCCCGGCCCCCAAGGGTCAGGAAGGCGGGCAGAGGCCGCGGGGAGAGGGAGCCGAGG A G SP2 Ensembl:ENSG00000167182 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:47896301..47896427 26863196 MeRIP-seq:(Medium) rs1290087461 Functional Loss SNV dbSNP153 33..33 33 - - - 97389 RMVar_ID_97389 Human_SNP_ID_625973104 m1A Human chr17 - 47902029 47902029 47902029 TATGTAAATTGCCACCCCCCTTTTTTTACCTTATCCTCATTTTGCCTCCTTAGCACTTCTCACTG TATGTAAATTGCCACCCCCCTTTTTTTACCTTTTCCTCATTTTGCCTCCTTAGCACTTCTCACTG T A SP2-AS1 Ensembl:ENSG00000234494 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47902024..47902151 26863196 MeRIP-seq:(Medium) rs760397312 Functional Loss SNV dbSNP153 33..33 33 - - - 97390 RMVar_ID_97390 Human_SNP_ID_625973152 m1A Human chr17 + 47902236 47902236 47902236 CAGCAGGGGCCATACTTGGTATGTTCAGGAACAGCAGGGAGCCAGCATGGCTAAAGCAGTGAGAG CAGCAGGGGCCATACTTGGTATGTTCAGGAACCGCAGGGAGCCAGCATGGCTAAAGCAGTGAGAG A C SP2 Ensembl:ENSG00000167182 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47902228..47902609 26863196 MeRIP-seq:(Medium) rs1252697498 Functional Loss SNV dbSNP153 33..33 33 - - - 97391 RMVar_ID_97391 Human_SNP_ID_625973677 m1A Human chr17 + 47904264 47904264 47904264 TCCAGCCTGGGTGACAGTGAGACTCTGTCCCAAAAAAAAAAAAAAAAAAGAAGTAGAAGTAGCCA TCCAGCCTGGGTGACAGTGAGACTCTGTCCCAGAAAAAAAAAAAAAAAAGAAGTAGAAGTAGCCA A G SP2 Ensembl:ENSG00000167182 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47904259..47904464 26863196 MeRIP-seq:(Medium) rs1428604077 Functional Loss SNV dbSNP153 33..33 33 - - - 97392 RMVar_ID_97392 Human_SNP_ID_625976400 m1A Human chr17 - 47916599 47916599 47916599 GACTTCTGGATGGGGGCTGGCTTGATGGGGACAGGCTTGTGACTGGACGGTGAGGGGGTGATGAT GACTTCTGGATGGGGGCTGGCTTGATGGGGACGGGCTTGTGACTGGACGGTGAGGGGGTGATGAT T C SP2-AS1 Ensembl:ENSG00000234494 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47916359..47916772 26863196 MeRIP-seq:(Medium) rs762056656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5649096 97393 RMVar_ID_97393 Human_SNP_ID_625976401 m1A Human chr17 - 47916599 47916599 47916599 GACTTCTGGATGGGGGCTGGCTTGATGGGGACAGGCTTGTGACTGGACGGTGAGGGGGTGATGAT GACTTCTGGATGGGGGCTGGCTTGATGGGGACCGGCTTGTGACTGGACGGTGAGGGGGTGATGAT T G SP2-AS1 Ensembl:ENSG00000234494 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47916359..47916772 26863196 MeRIP-seq:(Medium) rs762056656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5649096 97394 RMVar_ID_97394 Human_SNP_ID_625981382 m1A Human chr17 - 47937089 47937089 47937089 TTGTCTAAGTGGAAGGTGGGGGCAGGATCCTGATGCATGAGTATGGCGTAGGGCATGTGGAGAGG TTGTCTAAGTGGAAGGTGGGGGCAGGATCCTGTTGCATGAGTATGGCGTAGGGCATGTGGAGAGG T A SP2-AS1 Ensembl:ENSG00000234494 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47937044..47937138 26863196 MeRIP-seq:(Medium) rs1379412091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21974400 97395 RMVar_ID_97395 Human_SNP_ID_625982521 m1A Human chr17 - 47941698 47941698 47941698 GCCACTCGGCAGGTCGCCCGAACGTCGCCGTGACGCCCCGCAGCCAGCACGTCATGGGGGGCCGC GCCACTCGGCAGGTCGCCCGAACGTCGCCGTGGCGCCCCGCAGCCAGCACGTCATGGGGGGCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47941647..47941778 26863196 MeRIP-seq:(Medium) rs902178367 Functional Loss SNV dbSNP153 33..33 33 - - - 97396 RMVar_ID_97396 Human_SNP_ID_625982551 m1A Human chr17 + 47941769 47941769 47941769 ACCTCAGTCACCTGTGTGGTCGCAGTGCTGCCATGGACCTGGGACCCATGCGCAAGAGTTACCGC ACCTCAGTCACCTGTGTGGTCGCAGTGCTGCCGTGGACCTGGGACCCATGCGCAAGAGTTACCGC A G PNPO Ensembl:ENSG00000108439 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47941632..47942004 26863196 MeRIP-seq:(Medium) rs1406056157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235820,Human_RBP_ID_492123,Human_RBP_ID_1535934,Human_RBP_ID_4464635,Human_RBP_ID_6606195,Human_RBP_ID_13050921,Human_RBP_ID_18419641 Human_Splice_Rec_1833339,Human_Splice_Rec_1833363,Human_Splice_Rec_1833373,Human_Splice_Rec_1833383,Human_Splice_Rec_1833395,Human_Splice_Rec_1833403,Human_Splice_Rec_1833413,Human_Splice_Rec_1833419,Human_Splice_Rec_1833425,Human_Splice_Rec_1833437,Human_Splice_Rec_1833445,Human_Splice_Rec_1833453 RMVar_hsa_circ_93066,RMVar_hsa_circ_185056 97397 RMVar_ID_97397 Human_SNP_ID_625982607 m1A Human chr17 + 47941878 47941878 47941878 GCGGGGGAAAAGGGGTCCCCGGAGTCATCTACAGCGGGGAGGGGAGTAGTAGGAGCCCCTCGGGG GCGGGGGAAAAGGGGTCCCCGGAGTCATCTACTGCGGGGAGGGGAGTAGTAGGAGCCCCTCGGGG A T PNPO Ensembl:ENSG00000108439 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:47941849..47942004 26863196 MeRIP-seq:(Medium) rs1202736231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897698 RMVar_hsa_circ_93066,RMVar_hsa_circ_185056 97398 RMVar_ID_97398 Human_SNP_ID_625990251 m1A Human chr17 + 47973929 47973929 47973929 TTTAGTTCTCGAAATCCCGTCTCTTGCTTTCTAGACATTCACTACTTTCACTGCCTAAGAATCCT TTTAGTTCTCGAAATCCCGTCTCTTGCTTTCTGGACATTCACTACTTTCACTGCCTAAGAATCCT A G AC018521.1,CDK5RAP3 Ensembl:ENSG00000263798,Ensembl:ENSG00000108465 lincRNA,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47973926..47974000 32194978 MeRIP-seq:(Medium) rs763027669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952626,Human_RBP_ID_25294960 RMVar_hsa_circ_5074,RMVar_hsa_circ_77297,RMVar_hsa_circ_185063,RMVar_hsa_circ_357514,RMVar_hsa_circ_39158,RMVar_hsa_circ_72412,RMVar_hsa_circ_114438,RMVar_hsa_circ_121431,RMVar_hsa_circ_79313 97399 RMVar_ID_97399 Human_SNP_ID_625990430 m1A Human chr17 - 47974512 47974512 47974512 CACTCACAGACTGTGCCTCCTATAAGCCTGGTATCTCAGAACTCTGAGAGTGGGCTTCCCCATGG CACTCACAGACTGTGCCTCCTATAAGCCTGGTGTCTCAGAACTCTGAGAGTGGGCTTCCCCATGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47974464..47974813 32194978 MeRIP-seq:(Medium) rs974643235 Functional Loss SNV dbSNP153 33..33 33 - - - 97400 RMVar_ID_97400 Human_SNP_ID_625990505 m1A Human chr17 + 47974744 47974744 47974744 CACCTCTTGGTTAGCGGGAGTGTGCTGCCCCCACCCCCACCCCCGCACCCCCATTCTACACAAGG CACCTCTTGGTTAGCGGGAGTGTGCTGCCCCCCCCCCCACCCCCGCACCCCCATTCTACACAAGG A C AC018521.1,CDK5RAP3 Ensembl:ENSG00000263798,Ensembl:ENSG00000108465 lincRNA,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1444548943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22216039,Human_RBP_ID_23731677,Human_RBP_ID_26964266 RMVar_hsa_circ_5074,RMVar_hsa_circ_77297,RMVar_hsa_circ_185063,RMVar_hsa_circ_357514,RMVar_hsa_circ_39158,RMVar_hsa_circ_185065,RMVar_hsa_circ_72412,RMVar_hsa_circ_114438,RMVar_hsa_circ_121431,RMVar_hsa_circ_79313,RMVar_hsa_circ_185066,RMVar_hsa_circ_185067 97401 RMVar_ID_97401 Human_SNP_ID_625990936 m1A Human chr17 + 47975923 47975923 47975923 ATGCTGCGGTTCGTGCAGAAGCGGGGAAACTCAACGGTGTACGAGTGGAGGACAGGGACAGAGCC ATGCTGCGGTTCGTGCAGAAGCGGGGAAACTCTACGGTGTACGAGTGGAGGACAGGGACAGAGCC A T AC018521.1,CDK5RAP3 Ensembl:ENSG00000263798,Ensembl:ENSG00000108465 lincRNA,Protein coding exon,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:47975858..47975991 26863196 MeRIP-seq:(Medium) rs763529107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819549,Human_RBP_ID_901501,Human_RBP_ID_3548284,Human_RBP_ID_3952633,Human_RBP_ID_5579572,Human_RBP_ID_18988748,Human_RBP_ID_22959443,Human_RBP_ID_23731696,Human_RBP_ID_24559225,Human_RBP_ID_26331982 Human_Splice_Rec_1833512,Human_Splice_Rec_1833513,Human_Splice_Rec_1833550,Human_Splice_Rec_1833551,Human_Splice_Rec_1833586,Human_Splice_Rec_1833587,Human_Splice_Rec_1833631,Human_Splice_Rec_1833662,Human_Splice_Rec_1833663,Human_Splice_Rec_1833724,Human_Splice_Rec_1833725,Human_Splice_Rec_1833736,Human_Splice_Rec_1833737,Human_Splice_Rec_1833757,Human_Splice_Rec_1833814,Human_Splice_Rec_1833815,Human_Splice_Rec_1833841,Human_Splice_Rec_1833864,Human_Splice_Rec_1833865 RMVar_hsa_circ_5074,RMVar_hsa_circ_77297,RMVar_hsa_circ_185063,RMVar_hsa_circ_357514,RMVar_hsa_circ_39158,RMVar_hsa_circ_72412,RMVar_hsa_circ_121431,RMVar_hsa_circ_79313,RMVar_hsa_circ_185066,RMVar_hsa_circ_185067 97402 RMVar_ID_97402 Human_SNP_ID_625991134 m1A Human chr17 - 47976665 47976665 47976665 AGAGTGTTAGCTCATGGAAGATGGATTTAAAAAGGGCCGGGCATGGTGGCTCATGTCTGTAACCC AGAGTGTTAGCTCATGGAAGATGGATTTAAAAGGGGCCGGGCATGGTGGCTCATGTCTGTAACCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47976660..47976820 26863196 MeRIP-seq:(Medium) rs762429236 Functional Loss SNV dbSNP153 33..33 33 - - - 97403 RMVar_ID_97403 Human_SNP_ID_625991777 m1A Human chr17 - 47978919 47978919 47978919 GCCTCCCCCCTGCATCTTCCAGAGATGACAGTACCTCCATGAGCTCATCAAGGAACTGATTCCGG GCCTCCCCCCTGCATCTTCCAGAGATGACAGTGCCTCCATGAGCTCATCAAGGAACTGATTCCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47978826..47979234 32194978 MeRIP-seq:(Medium) rs745688199 Functional Loss SNV dbSNP153 33..33 33 - - - 97404 RMVar_ID_97404 Human_SNP_ID_626004457 m1A Human chr17 + 48032053 48032053 48032053 ATGGGATCCCTGGGAATATGCTGGGGGAAGGGAGTGAGAAGTTGGTCAGAGTTCTAGCCATGCTG ATGGGATCCCTGGGAATATGCTGGGGGAAGGGTGTGAGAAGTTGGTCAGAGTTCTAGCCATGCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48032049..48032137 26863196 MeRIP-seq:(Medium) rs913038130 Functional Loss SNV dbSNP153 33..33 33 - - - 97405 RMVar_ID_97405 Human_SNP_ID_626005920 m1A Human chr17 - 48037773 48037773 48037773 GCGCTGTCAGTGCGAGGCGGCGAGCGGAATGCAGCGGCCCGAGGCCTGGCCACGTCCGCACCCGG GCGCTGTCAGTGCGAGGCGGCGAGCGGAATGCTGCGGCCCGAGGCCTGGCCACGTCCGCACCCGG T A COPZ2 Ensembl:ENSG00000005243 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr17:48036874..48037867;chr17:48033920..48037853;chr17:48037677..48037806 26863196 MeRIP-seq:(Medium) rs1307831518 Functional Loss SNV dbSNP153 33..33 33 - - - 97406 RMVar_ID_97406 Human_SNP_ID_626005922 m1A Human chr17 - 48037777 48037776 48037777 GGCGGCGCTGTCAGTGCGAGGCGGCGAGCGGAATGCAGCGGCCCGAGGCCTGGCCACGTCCGCAC GGCGGCGCTGTCAGTGCGAGGCGGCGAGCGGA_TGCAGCGGCCCGAGGCCTGGCCACGTCCGCAC AT A COPZ2 Ensembl:ENSG00000005243 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48036909..48037886 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 33..33 33 - - - 97407 RMVar_ID_97407 Human_SNP_ID_626005923 m1A Human chr17 - 48037777 48037777 48037777 GGCGGCGCTGTCAGTGCGAGGCGGCGAGCGGAATGCAGCGGCCCGAGGCCTGGCCACGTCCGCAC GGCGGCGCTGTCAGTGCGAGGCGGCGAGCGGAGTGCAGCGGCCCGAGGCCTGGCCACGTCCGCAC T C COPZ2 Ensembl:ENSG00000005243 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48036909..48037886 26863196 MeRIP-seq:(Medium) rs1249429852 Functional Loss SNV dbSNP153 33..33 33 - - - 97408 RMVar_ID_97408 Human_SNP_ID_626005928 m1A Human chr17 - 48037783 48037783 48037783 GCGGCGGGCGGCGCTGTCAGTGCGAGGCGGCGAGCGGAATGCAGCGGCCCGAGGCCTGGCCACGT GCGGCGGGCGGCGCTGTCAGTGCGAGGCGGCGGGCGGAATGCAGCGGCCCGAGGCCTGGCCACGT T C COPZ2 Ensembl:ENSG00000005243 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:48037664..48037796 26863196 MeRIP-seq:(Medium) rs1487853038 Functional Loss SNV dbSNP153 33..33 33 - - - 97409 RMVar_ID_97409 Human_SNP_ID_626008467 m1A Human chr17 + 48047668 48047668 48047668 CCAACGTTCCGCCAACGTTCCGCCAACGTCCCACCACCCTCATGATATCCGTCCGCGGTACTGCT CCAACGTTCCGCCAACGTTCCGCCAACGTCCCGCCACCCTCATGATATCCGTCCGCGGTACTGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48047617..48047711 26863196 MeRIP-seq:(Medium) rs1055950303 Functional Loss SNV dbSNP153 33..33 33 - - - 97410 RMVar_ID_97410 Human_SNP_ID_626009423 m1A Human chr17 + 48050663 48050663 48050663 AGTGTGGAGGAGGCGGGACACTCTGACCCAAGACGAAAGGCCTGTAGCTCCAGCCAAAGAAAATA AGTGTGGAGGAGGCGGGACACTCTGACCCAAGGCGAAAGGCCTGTAGCTCCAGCCAAAGAAAATA A G NFE2L1 Ensembl:ENSG00000082641 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48048875..48051074 32194978 MeRIP-seq:(Medium) rs1318019079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237556,Human_RBP_ID_819902,Human_RBP_ID_1535993,Human_RBP_ID_4434559,Human_RBP_ID_5088256,Human_RBP_ID_5319093,Human_RBP_ID_6606432,Human_RBP_ID_8455367,Human_RBP_ID_8825625,Human_RBP_ID_8941829,Human_RBP_ID_13051817,Human_RBP_ID_22586320,Human_RBP_ID_22959233 Human_Splice_Rec_1833996,Human_Splice_Rec_1833998,Human_Splice_Rec_1834002,Human_Splice_Rec_1834012,Human_Splice_Rec_1834022,Human_Splice_Rec_1834030,Human_Splice_Rec_1834032,Human_Splice_Rec_1834034,Human_Splice_Rec_1834044,Human_Splice_Rec_1834046,Human_Splice_Rec_1834048,Human_Splice_Rec_1834052 RMVar_hsa_circ_71241,RMVar_hsa_circ_350476 97411 RMVar_ID_97411 Human_SNP_ID_626011470 m1A Human chr17 + 48058382 48058382 48058382 ACCCACTGAGCACCAACTACAGCCTTGCCCCCAACACTCCCATCAATCAGAATGTCAGCCTGCAT ACCCACTGAGCACCAACTACAGCCTTGCCCCCCACACTCCCATCAATCAGAATGTCAGCCTGCAT A C NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48058333..48058619 26863196 MeRIP-seq:(Medium) rs754333657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50305,Human_RBP_ID_9073051,Human_RBP_ID_17260326,Human_RBP_ID_17376122,Human_RBP_ID_17692306,Human_RBP_ID_17894582,Human_RBP_ID_22443037,Human_RBP_ID_22499724,Human_RBP_ID_22805225,Human_RBP_ID_26333506,Human_RBP_ID_27453707 Human_Splice_Rec_1834010,Human_Splice_Rec_1834020,Human_Splice_Rec_1834028,Human_Splice_Rec_1834042,Human_Splice_Rec_1834062,Human_Splice_Rec_1834068,Human_Splice_Rec_1834076,Human_Splice_Rec_1834086,Human_Splice_Rec_1834092,Human_Splice_Rec_1834098,Human_Splice_Rec_1834104,Human_Splice_Rec_1834110 97412 RMVar_ID_97412 Human_SNP_ID_626011523 m1A Human chr17 + 48058526 48058526 48058526 CCACGCTGCTCCCGTTGGCCCCCAGCAATTCTACCAGCCTCAACTCCACCTTCGGCTCCACCAAC CCACGCTGCTCCCGTTGGCCCCCAGCAATTCTCCCAGCCTCAACTCCACCTTCGGCTCCACCAAC A C NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:48058501..48058525 26863196 MeRIP-seq:(Medium) rs768460676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1008760,Human_RBP_ID_1238803,Human_RBP_ID_3526723,Human_RBP_ID_6606522,Human_RBP_ID_17260328,Human_RBP_ID_17376124,Human_RBP_ID_17491887,Human_RBP_ID_18190885,Human_RBP_ID_18700901,Human_RBP_ID_27453713 97413 RMVar_ID_97413 Human_SNP_ID_626011524 m1A Human chr17 + 48058526 48058526 48058526 CCACGCTGCTCCCGTTGGCCCCCAGCAATTCTACCAGCCTCAACTCCACCTTCGGCTCCACCAAC CCACGCTGCTCCCGTTGGCCCCCAGCAATTCTGCCAGCCTCAACTCCACCTTCGGCTCCACCAAC A G NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:48058501..48058525 26863196 MeRIP-seq:(Medium) rs768460676 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1008760,Human_RBP_ID_1238803,Human_RBP_ID_3526723,Human_RBP_ID_6606522,Human_RBP_ID_17260328,Human_RBP_ID_17376124,Human_RBP_ID_17491887,Human_RBP_ID_18190885,Human_RBP_ID_18700901,Human_RBP_ID_27453713 97414 RMVar_ID_97414 Human_SNP_ID_626011724 m1A Human chr17 + 48058999 48058999 48058999 TCCAAGTTCTGCCGCATGAGCTACCAGGATCCAGCTCAGCTCTCATGCCTGCCCTACCTGGAGCA TCCAAGTTCTGCCGCATGAGCTACCAGGATCCTGCTCAGCTCTCATGCCTGCCCTACCTGGAGCA A T NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48058951..48059000 32194978 MeRIP-seq:(Medium) rs749998101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492202,Human_RBP_ID_768079,Human_RBP_ID_1536039,Human_RBP_ID_5525673,Human_RBP_ID_6606533,Human_RBP_ID_8819106,Human_RBP_ID_18470075,Human_RBP_ID_22761122,Human_RBP_ID_27453729 97415 RMVar_ID_97415 Human_SNP_ID_626012250 m1A Human chr17 + 48060326 48060326 48060326 GTTTCAATCGAATGGAGCCACTGGGCCCCAACACTGGCTTTGAGATTTAGAGTCAAAGGGTAGAG GTTTCAATCGAATGGAGCCACTGGGCCCCAACGCTGGCTTTGAGATTTAGAGTCAAAGGGTAGAG A G NFE2L1 Ensembl:ENSG00000082641 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48060276..48060325 32194978 MeRIP-seq:(Medium) rs1412536353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492216,Human_RBP_ID_1861243,Human_RBP_ID_8191207,Human_RBP_ID_8455409,Human_RBP_ID_17894601,Human_RBP_ID_23731774,Human_RBP_ID_26457848,Human_RBP_ID_26812511 Human_miRNA_ID_505100,Human_miRNA_ID_512308 97416 RMVar_ID_97416 Human_SNP_ID_626012264 m1A Human chr17 + 48060385 48060385 48060385 GTAGAGTGAACAGGAAAGGGTCACGTGGTCCCATGTTGCAACAGCCCCAACATCACGCATGTCAT GTAGAGTGAACAGGAAAGGGTCACGTGGTCCCCTGTTGCAACAGCCCCAACATCACGCATGTCAT A C NFE2L1 Ensembl:ENSG00000082641 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:48060335..48060537 26863196 MeRIP-seq:(Medium) rs1293731451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536062,Human_RBP_ID_8192071,Human_RBP_ID_17260339,Human_RBP_ID_17904397,Human_RBP_ID_20227682,Human_RBP_ID_26457849 97417 RMVar_ID_97417 Human_SNP_ID_626012281 m1A Human chr17 - 48060450 48060450 48060450 GACAATGGGAGCCTCAGCTCAGGGGTGGCTGGAGCACGGAGGGAGATGGAGTGGCAAGGCAGTGA GACAATGGGAGCCTCAGCTCAGGGGTGGCTGGTGCACGGAGGGAGATGGAGTGGCAAGGCAGTGA T A AC004477.2 Ensembl:ENSG00000266341 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48060351..48060450 32194978 MeRIP-seq:(Medium) rs1477714951 Functional Loss SNV dbSNP153 33..33 33 - - - 97418 RMVar_ID_97418 Human_SNP_ID_626014934 m1A Human chr17 + 48070327 48070326 48070327 TTAAAGTGAACCACTGCCCAATATGAAAGTTTAATCTTCTCCTGAGACCAAGGCTTTTGAAATCA TTAAAGTGAACCACTGCCCAATATGAAAGTTT_ATCTTCTCCTGAGACCAAGGCTTTTGAAATCA TA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48070276..48070350 32194978 MeRIP-seq:(Medium) rs1479102235 Functional Loss DEL dbSNP153 33..33 33 - - - 97419 RMVar_ID_97419 Human_SNP_ID_626015150 m1A Human chr17 - 48071225 48071224 48071225 TTGCACACCCATCCCAGTGGAGGGGAAAGGGGATAAGTGTTTCAAGGCAACCTTTTCTGCACTTT TTGCACACCCATCCCAGTGGAGGGGAAAGGGG_TAAGTGTTTCAAGGCAACCTTTTCTGCACTTT AT A CBX1 Ensembl:ENSG00000108468 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48071176..48071250 32194978 MeRIP-seq:(Medium) rs1250923386 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_492271,Human_RBP_ID_1008789,Human_RBP_ID_1536080,Human_RBP_ID_1861264,Human_RBP_ID_17894643,Human_RBP_ID_21890761,Human_RBP_ID_27255863 RMVar_hsa_circ_115839,RMVar_hsa_circ_185078 97420 RMVar_ID_97420 Human_SNP_ID_626015151 m1A Human chr17 - 48071225 48071225 48071225 TTGCACACCCATCCCAGTGGAGGGGAAAGGGGATAAGTGTTTCAAGGCAACCTTTTCTGCACTTT TTGCACACCCATCCCAGTGGAGGGGAAAGGGGGTAAGTGTTTCAAGGCAACCTTTTCTGCACTTT T C CBX1 Ensembl:ENSG00000108468 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48071176..48071250 32194978 MeRIP-seq:(Medium) rs1459053310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492271,Human_RBP_ID_1008789,Human_RBP_ID_1536080,Human_RBP_ID_1861264,Human_RBP_ID_17894643,Human_RBP_ID_21890761,Human_RBP_ID_27255863 RMVar_hsa_circ_115839,RMVar_hsa_circ_185078 97421 RMVar_ID_97421 Human_SNP_ID_626015201 m1A Human chr17 - 48071445 48071445 48071445 CTACCCCTCGGAGGATGATGACAAAAAAGATGACAAGAACTAACGCTCCTGAGTACCAGCCCCTG CTACCCCTCGGAGGATGATGACAAAAAAGATGGCAAGAACTAACGCTCCTGAGTACCAGCCCCTG T C CBX1 Ensembl:ENSG00000108468 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48071395..48071495 32194978 MeRIP-seq:(Medium) rs202111986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492276,Human_RBP_ID_1008791,Human_RBP_ID_1536081,Human_RBP_ID_1861265,Human_RBP_ID_13052100,Human_RBP_ID_17653867,Human_RBP_ID_18700931,Human_RBP_ID_27453795 RMVar_hsa_circ_115839,RMVar_hsa_circ_185078 97422 RMVar_ID_97422 Human_SNP_ID_626015223 m1A Human chr17 - 48071577 48071577 48071577 CTCAAAGTCTCTCTTTGCTTTATTCTGCAGGAAAAACTCTGATGAGGCTGACCTGGTCCCTGCCA CTCAAAGTCTCTCTTTGCTTTATTCTGCAGGAGAAACTCTGATGAGGCTGACCTGGTCCCTGCCA T C CBX1 Ensembl:ENSG00000108468 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48071526..48071600 32194978 MeRIP-seq:(Medium) rs756109344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492277 Human_Splice_Rec_1834120,Human_Splice_Rec_1834128,Human_Splice_Rec_1834138,Human_Splice_Rec_1834146 RMVar_hsa_circ_115839,RMVar_hsa_circ_185078 97423 RMVar_ID_97423 Human_SNP_ID_626016395 m1A Human chr17 + 48076094 48076094 48076094 TTGCGCTTGCCTCCCTCTGATTTATCTGTCTCATGTGCTGTTTTCTGTGACTGCAGAAACTCAGC TTGCGCTTGCCTCCCTCTGATTTATCTGTCTCGTGTGCTGTTTTCTGTGACTGCAGAAACTCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48076043..48076203 26863196 MeRIP-seq:(Medium) rs902121024 Functional Loss SNV dbSNP153 33..33 33 - - - 97424 RMVar_ID_97424 Human_SNP_ID_626016572 m1A Human chr17 - 48076945 48076945 48076945 GTGGAGGAGGTGCTAGAAGAGGAGGAAGAGGAATATGTGGTGGAAAAAGTTCTCGACCGTCGAGT GTGGAGGAGGTGCTAGAAGAGGAGGAAGAGGAGTATGTGGTGGAAAAAGTTCTCGACCGTCGAGT T C CBX1 Ensembl:ENSG00000108468 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48076851..48077064 26863196 MeRIP-seq:(Medium) rs200247402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492285,Human_RBP_ID_3526759,Human_RBP_ID_4474794,Human_RBP_ID_6606689,Human_RBP_ID_9346329,Human_RBP_ID_17653868,Human_RBP_ID_24544884 Human_Splice_Rec_1834114,Human_Splice_Rec_1834115,Human_Splice_Rec_1834122,Human_Splice_Rec_1834123,Human_Splice_Rec_1834132,Human_Splice_Rec_1834133,Human_Splice_Rec_1834140,Human_Splice_Rec_1834141,Human_Splice_Rec_1834148,Human_Splice_Rec_1834149,Human_Splice_Rec_1834156,Human_Splice_Rec_1834157 Human_miRNA_ID_3064955 RMVar_hsa_circ_8149,RMVar_hsa_circ_115839,RMVar_hsa_circ_185079,RMVar_hsa_circ_185078,RMVar_hsa_circ_327132,RMVar_hsa_circ_284817 97425 RMVar_ID_97425 Human_SNP_ID_626023489 m1A Human chr17 - 48101063 48101063 48101063 AGGCGTCGGTGCCAGCTGCGTGAAGGATGGAGAGGGCGGGGCGCGAATCCTGAGCCAGAGACTGA AGGCGTCGGTGCCAGCTGCGTGAAGGATGGAGGGGGCGGGGCGCGAATCCTGAGCCAGAGACTGA T C CBX1 Ensembl:ENSG00000108468 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:48100871..48101119 26863196 MeRIP-seq:(Medium) rs997572314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22499729,Human_RBP_ID_26758838 97426 RMVar_ID_97426 Human_SNP_ID_626026497 m1A Human chr17 + 48112005 48112005 48112005 AGAATGATAAGAACAGAGGCATACTAACCTTGATCCTGTATCCTCTGTCCCTCATCAGATGTTTC AGAATGATAAGAACAGAGGCATACTAACCTTGTTCCTGTATCCTCTGTCCCTCATCAGATGTTTC A T SNX11 Ensembl:ENSG00000002919 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48112003..48112218 26863196 MeRIP-seq:(Medium) rs746019694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_900278,Human_RBP_ID_23731845 Human_Splice_Rec_1834163,Human_Splice_Rec_1834205,Human_Splice_Rec_1834221,Human_Splice_Rec_1834231,Human_Splice_Rec_1834243,Human_Splice_Rec_1834267,Human_Splice_Rec_1834277 RMVar_hsa_circ_185080,RMVar_hsa_circ_78911 97427 RMVar_ID_97427 Human_SNP_ID_626026531 m1A Human chr17 - 48112087 48112087 48112087 TTACCCACCTGTTCTCTGCAGACCATACTCTTACCTCCTGTTCTTGGTTCTCCGACATCCTACAC TTACCCACCTGTTCTCTGCAGACCATACTCTTTCCTCCTGTTCTTGGTTCTCCGACATCCTACAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48112014..48112146 26863196 MeRIP-seq:(Medium) rs1303995851 Functional Loss SNV dbSNP153 33..33 33 - - - 97428 RMVar_ID_97428 Human_SNP_ID_626120357 m1A Human chr17 - 48543122 48543122 48543122 TCTCTCGACAGCCCGGTCCCTTTTTCCGAGGAAGAGCTGGATTTTTTCACCAGTACGCTCTGTGC TCTCTCGACAGCCCGGTCCCTTTTTCCGAGGAGGAGCTGGATTTTTTCACCAGTACGCTCTGTGC T C HOXB2 Ensembl:ENSG00000173917 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48541626..48543325 32194978 MeRIP-seq:(Medium) rs566624251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536117,Human_RBP_ID_17491933,Human_RBP_ID_17894727,Human_RBP_ID_22499735,Human_RBP_ID_26459463,Human_RBP_ID_27666185 97429 RMVar_ID_97429 Human_SNP_ID_626120646 m1A Human chr17 - 48543576 48543576 48543576 GGCCTTGCTGGACCTCACCGAAAGGCAGGTCAAAGTCTGGTTTCAGAACCGGCGCATGAAGCACA GGCCTTGCTGGACCTCACCGAAAGGCAGGTCAGAGTCTGGTTTCAGAACCGGCGCATGAAGCACA T C HOXB2 Ensembl:ENSG00000173917 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48543253..48543703 32194978 MeRIP-seq:(Medium) rs768353568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536118,Human_RBP_ID_4435105,Human_RBP_ID_8455469 97430 RMVar_ID_97430 Human_SNP_ID_626121099 m1A Human chr17 - 48544694 48544694 48544694 CCTTCAGAGACCCAGGAGCCAAAAGCGAGCCGAAGATGGGCCTGCTCTGCCGCCGCCACCGCCGC CCTTCAGAGACCCAGGAGCCAAAAGCGAGCCGCAGATGGGCCTGCTCTGCCGCCGCCACCGCCGC T G HOXB2 Ensembl:ENSG00000173917 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:48544597..48544737 26863410 MeRIP-seq:(Medium) rs758916067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13052869,Human_RBP_ID_17378426,Human_RBP_ID_22443038 97431 RMVar_ID_97431 Human_SNP_ID_626121145 m1A Human chr17 - 48544789 48544789 48544789 ACATTTCAAACTTCATCAATCAAGGAGTCGACATTAATTCCTCCTCCTCCTCCTTTCGAGCAAAC ACATTTCAAACTTCATCAATCAAGGAGTCGACGTTAATTCCTCCTCCTCCTCCTTTCGAGCAAAC T C HOXB2 Ensembl:ENSG00000173917 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48544738..48544839 32194978 MeRIP-seq:(Medium) rs1555633354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536122,Human_RBP_ID_5441563,Human_RBP_ID_5497216,Human_RBP_ID_9326710,Human_RBP_ID_17260390,Human_RBP_ID_17894738,Human_RBP_ID_23275789 97432 RMVar_ID_97432 Human_SNP_ID_626121335 m1A Human chr17 - 48545221 48545221 48545221 TCCTGGTCGTGGTCCTCTGGTGTTTTTGAATCAATTAAACCAAATAATGCTCTCTGTTTTCCACC TCCTGGTCGTGGTCCTCTGGTGTTTTTGAATCGATTAAACCAAATAATGCTCTCTGTTTTCCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48545214..48545596 32194978 MeRIP-seq:(Medium) rs559610244 Functional Loss SNV dbSNP153 33..33 33 - - - 97433 RMVar_ID_97433 Human_SNP_ID_626122780 m1A Human chr17 - 48550470 48550470 48550470 TTCCCATCACCCTTCCGGGAACCTGGACTACAACGGGGCGCCCCCTATGGCGCCCAGCCAGCACC TTCCCATCACCCTTCCGGGAACCTGGACTACACCGGGGCGCCCCCTATGGCGCCCAGCCAGCACC T G HOXB3 Ensembl:ENSG00000120093 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:48550419..48550527 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_17260395 RMVar_hsa_circ_78799,RMVar_hsa_circ_185091 97434 RMVar_ID_97434 Human_SNP_ID_626122930 m1A Human chr17 + 48550719 48550719 48550719 AGCCTTTGAGAGGGGGCTGGTAGTTGGAGGGCAGCGCGTAGGCATTCTGGTGGGCTTTACCGAAG AGCCTTTGAGAGGGGGCTGGTAGTTGGAGGGCCGCGCGTAGGCATTCTGGTGGGCTTTACCGAAG A C HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48550672..48550865 26863196 MeRIP-seq:(Medium) rs751235759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18544411 97435 RMVar_ID_97435 Human_SNP_ID_626122931 m1A Human chr17 + 48550719 48550719 48550719 AGCCTTTGAGAGGGGGCTGGTAGTTGGAGGGCAGCGCGTAGGCATTCTGGTGGGCTTTACCGAAG AGCCTTTGAGAGGGGGCTGGTAGTTGGAGGGCGGCGCGTAGGCATTCTGGTGGGCTTTACCGAAG A G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48550672..48550865 26863196 MeRIP-seq:(Medium) rs751235759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18544411 97436 RMVar_ID_97436 Human_SNP_ID_626123144 m1A Human chr17 + 48551156 48551141 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCT_______________CCGCCGCCGCCACCACAGCCCTCTGCTGGATC TCCGCCGCCGCCGCCA T HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs766375333 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_9326712 97437 RMVar_ID_97437 Human_SNP_ID_626123151 m1A Human chr17 + 48551156 48551144 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCG____________CCGCCGCCGCCACCACAGCCCTCTGCTGGATC GCCGCCGCCGCCA G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs752394950 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_9326712 97438 RMVar_ID_97438 Human_SNP_ID_626123154 m1A Human chr17 + 48551156 48551147 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCGCCG_________CCGCCGCCGCCACCACAGCCCTCTGCTGGATC GCCGCCGCCA G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs763638422 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_9326712 97439 RMVar_ID_97439 Human_SNP_ID_626123159 m1A Human chr17 + 48551156 48551150 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCGCCGCCG______CCGCCGCCGCCACCACAGCCCTCTGCTGGATC GCCGCCA G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs753409967 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_9326712 97440 RMVar_ID_97440 Human_SNP_ID_626123164 m1A Human chr17 + 48551156 48551153 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCGCCGCCGCCG___CCGCCGCCGCCACCACAGCCCTCTGCTGGATC GCCA G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs755319933 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_9326712 97441 RMVar_ID_97441 Human_SNP_ID_626123166 m1A Human chr17 + 48551156 48551156 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCGCCGCCGCCGCCACCACAGCCCTCTGCTGGATC A G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs559346033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326712 97442 RMVar_ID_97442 Human_SNP_ID_626125545 m1A Human chr17 - 48558917 48558915 48558917 CTCTCTCTCACACACACACACACCCTACACACATGGGCACACACACACAGTTTTCCAGGTTTCCC CTCTCTCTCACACACACACACACCCTACACAC__GGGCACACACACACAGTTTTCCAGGTTTCCC CAT C HOXB3 Ensembl:ENSG00000120093 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:48558910..48558994 26863196 MeRIP-seq:(Medium) rs1268106085 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_20228128 97443 RMVar_ID_97443 Human_SNP_ID_626126864 m1A Human chr17 - 48564317 48564317 48564317 AGCGACTAGGATGCGGCTGGCTGCGGCGGCGGAGCCCCAGCCTGGGCCGAGGGTCCGGGGCCTGG AGCGACTAGGATGCGGCTGGCTGCGGCGGCGGGGCCCCAGCCTGGGCCGAGGGTCCGGGGCCTGG T C HOXB3 Ensembl:ENSG00000120093 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48564311..48564376 26863196 MeRIP-seq:(Medium) rs1015853093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262646,Human_RBP_ID_3541752 97444 RMVar_ID_97444 Human_SNP_ID_626129754 m1A Human chr17 + 48576206 48576206 48576206 TATCGGGAGTGGGGGACAAAGAAAGGAAATCCAGGCTGTCTTCCAGCAGCGGCAGTAGCAGAGGC TATCGGGAGTGGGGGACAAAGAAAGGAAATCCGGGCTGTCTTCCAGCAGCGGCAGTAGCAGAGGC A G HOXB-AS3 Ensembl:ENSG00000233101 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48576105..48576205 32194978 MeRIP-seq:(Medium) rs904206758 Functional Loss SNV dbSNP153 33..33 33 - - - 97445 RMVar_ID_97445 Human_SNP_ID_626132245 m1A Human chr17 - 48584805 48584805 48584805 AGTGGGGGAGCAGAAATGGGCAGCGAAGAGGCAGATATCTGGGGAAGGGAAACTGAGGAAGGAAA AGTGGGGGAGCAGAAATGGGCAGCGAAGAGGCGGATATCTGGGGAAGGGAAACTGAGGAAGGAAA T C HOXB3 Ensembl:ENSG00000120093 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48584779..48584852 26863196 MeRIP-seq:(Medium) rs1220197574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6607503,Human_RBP_ID_13054060,Human_RBP_ID_22953302,Human_RBP_ID_23732227 97446 RMVar_ID_97446 Human_SNP_ID_626135434 m1A Human chr17 - 48596361 48596360 48596361 AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGAGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCG_GGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT CT C HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1555644357 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17894833,Human_RBP_ID_22715756 97447 RMVar_ID_97447 Human_SNP_ID_626135435 m1A Human chr17 - 48596361 48596361 48596361 AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGAGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGCGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT T G HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12949148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17894833,Human_RBP_ID_22715756 97448 RMVar_ID_97448 Human_SNP_ID_626135436 m1A Human chr17 - 48596361 48596361 48596362 AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGAGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCACGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT TC GT HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35574633 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_17894833,Human_RBP_ID_22715756 97449 RMVar_ID_97449 Human_SNP_ID_626135710 m1A Human chr17 + 48597281 48597280 48597282 TCATCTTGCCCCAGCTCCCCACCCACAGGGAAACACAGTCCCAGACAGACTCAACTCTTTCTCTT TCATCTTGCCCCAGCTCCCCACCCACAGGGAA__ACAGTCCCAGACAGACTCAACTCTTTCTCTT AAC A HOXB-AS3 Ensembl:ENSG00000233101 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48597088..48597313 26863196 MeRIP-seq:(Medium) rs1240728456 Functional Loss DEL dbSNP153 33..34 33 - - - 97450 RMVar_ID_97450 Human_SNP_ID_626136042 m1A Human chr17 - 48598056 48598056 48598056 CCTGGGCCAGCTACCGCTCTATTCGTCGGGCTATGCGGACCCGCTGAGACATTACCCCGCGCCCT CCTGGGCCAGCTACCGCTCTATTCGTCGGGCTCTGCGGACCCGCTGAGACATTACCCCGCGCCCT T G HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48598011..48598160 32194978 MeRIP-seq:(Medium) rs1395097584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1861444,Human_RBP_ID_20229003,Human_RBP_ID_22953366,Human_RBP_ID_26964783,Human_RBP_ID_27453858 97451 RMVar_ID_97451 Human_SNP_ID_626137661 m1A Human chr17 - 48604258 48604258 48604258 GCCAAGGCAGGGAAAGCGGGAAGAGGAATCAAAAGAGGGCCAGGAGACCAGCTCTAAGTCGCCTT GCCAAGGCAGGGAAAGCGGGAAGAGGAATCAAGAGAGGGCCAGGAGACCAGCTCTAAGTCGCCTT T C HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48604207..48604321 26863196 MeRIP-seq:(Medium) rs1316975032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2510909,Human_RBP_ID_22216470,Human_RBP_ID_22586343,Human_RBP_ID_25343798,Human_RBP_ID_26964896 97452 RMVar_ID_97452 Human_SNP_ID_626138622 m1A Human chr17 - 48607955 48607955 48607955 TCGCGCACACGCTCTGCCTCACGGAAAGACAGATCAAGATTTGGTTTCAGAACCGGCGCATGAAG TCGCGCACACGCTCTGCCTCACGGAAAGACAGTTCAAGATTTGGTTTCAGAACCGGCGCATGAAG T A HOXB7 Ensembl:ENSG00000260027 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48607726..48608000 32194978 MeRIP-seq:(Medium) rs748360244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536236,Human_RBP_ID_1861482,Human_RBP_ID_3526991 97453 RMVar_ID_97453 Human_SNP_ID_626142916 m1A Human chr17 - 48621502 48621502 48621502 GGGAAACAGTCCCGCGTGCAAAGGAAAGGGGCAAAATGGCACCTAAGCATCAGATGGAAGCTTAC GGGAAACAGTCCCGCGTGCAAAGGAAAGGGGCGAAATGGCACCTAAGCATCAGATGGAAGCTTAC T C HOXB9,HOXB7 Ensembl:ENSG00000170689,Ensembl:ENSG00000260027 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48621456..48621804 32194978 MeRIP-seq:(Medium) rs1425846641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492479,Human_RBP_ID_5319123,Human_RBP_ID_8455644,Human_RBP_ID_23732423 97454 RMVar_ID_97454 Human_SNP_ID_626144034 m1A Human chr17 + 48625544 48625544 48625544 CTGTTCCCCGCAGGACTTGGAGAAGTGGGGGCAGCGCTCCTCTGGCGGCCTCAGTCTCCCCTTCT CTGTTCCCCGCAGGACTTGGAGAAGTGGGGGCTGCGCTCCTCTGGCGGCCTCAGTCTCCCCTTCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:48625493..48625683 26863196 MeRIP-seq:(Medium) rs942905168 Functional Loss SNV dbSNP153 33..33 33 - - - 97455 RMVar_ID_97455 Human_SNP_ID_626144172 m1A Human chr17 - 48625878 48625878 48625878 GCTGCTGGGCGCGCCTGGGGAGCTGCTCAAACAGGGCACGCCCGAGTACAGTTTGGAAACTTCGG GCTGCTGGGCGCGCCTGGGGAGCTGCTCAAACCGGGCACGCCCGAGTACAGTTTGGAAACTTCGG T G HOXB9,HOXB7 Ensembl:ENSG00000170689,Ensembl:ENSG00000260027 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48625723..48625902 26863196 MeRIP-seq:(Medium) rs1467629850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4474978,Human_RBP_ID_5420197,Human_RBP_ID_8941833,Human_RBP_ID_17894920,Human_RBP_ID_18701238,Human_RBP_ID_26965103,Human_RBP_ID_27256168 97456 RMVar_ID_97456 Human_SNP_ID_626144301 m1A Human chr17 - 48626105 48626104 48626105 CTGGAGTTCCCCTCGTGCAGCTTCCAGCCCAAAGCGCCGGTGTTCGGCGCCTCCTGGGCGCCGCT CTGGAGTTCCCCTCGTGCAGCTTCCAGCCCAA_GCGCCGGTGTTCGGCGCCTCCTGGGCGCCGCT CT C HOXB9,HOXB7 Ensembl:ENSG00000170689,Ensembl:ENSG00000260027 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:48625826..48626132 26863410 MeRIP-seq:(Medium) rs1235387939 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_492529,Human_RBP_ID_4435617,Human_RBP_ID_5466634,Human_RBP_ID_6607895,Human_RBP_ID_18701239,Human_RBP_ID_23732469,Human_RBP_ID_26965106 97457 RMVar_ID_97457 Human_SNP_ID_626144467 m1A Human chr17 - 48626462 48626462 48626462 TCGGAAAAACTTTGACCAATCATTTTGCAAGGAGAGCTGAGACGGGCTGCTCCACTGTACTTTGT TCGGAAAAACTTTGACCAATCATTTTGCAAGGGGAGCTGAGACGGGCTGCTCCACTGTACTTTGT T C HOXB7 Ensembl:ENSG00000260027 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:48626451..48626577 26863196 MeRIP-seq:(Medium) rs1164506095 Functional Loss SNV dbSNP153 33..33 33 - - - 97458 RMVar_ID_97458 Human_SNP_ID_626149477 m1A Human chr17 - 48646743 48646743 48646743 GCGTCGCTGCCCCAGACACAGACACTGCCTCGAGAGGCCTCACAGAGGCGGGGGCAGAAGGCGGC GCGTCGCTGCCCCAGACACAGACACTGCCTCGGGAGGCCTCACAGAGGCGGGGGCAGAAGGCGGC T C AC103702.2 Ensembl:ENSG00000272763 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48646698..48646812 26863196 MeRIP-seq:(Medium) rs1363873930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465511 97459 RMVar_ID_97459 Human_SNP_ID_626169343 m1A Human chr17 - 48725280 48725279 48725281 GTGTGAGTGCATGCGGACTGGGGGTTCAGGGGAAGAGGACGAGGAGGAGGAAGATGAGGTCGATT GTGTGAGTGCATGCGGACTGGGGGTTCAGGG__AGAGGACGAGGAGGAGGAAGATGAGGTCGATT TTC T HOXB13 Ensembl:ENSG00000159184 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:48725232..48725399 26863196 MeRIP-seq:(Medium) rs1303964456 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6607993 97460 RMVar_ID_97460 Human_SNP_ID_626169351 m1A Human chr17 + 48725301 48725301 48725301 CCTCGTCCTCTTCCCCTGAACCCCCAGTCCGCATGCACTCACACTCTTTGGCCTTTTCCCTCAGT CCTCGTCCTCTTCCCCTGAACCCCCAGTCCGCGTGCACTCACACTCTTTGGCCTTTTCCCTCAGT A G NONHSAG022094.2 RNACentral:URS00009C429B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48725209..48725417 26863196 MeRIP-seq:(Medium) rs1167232380 Functional Loss SNV dbSNP153 33..33 33 - - - 97461 RMVar_ID_97461 Human_SNP_ID_626169352 m1A Human chr17 - 48725302 48725302 48725302 GACTGAGGGAAAAGGCCAAAGAGTGTGAGTGCATGCGGACTGGGGGTTCAGGGGAAGAGGACGAG GACTGAGGGAAAAGGCCAAAGAGTGTGAGTGCCTGCGGACTGGGGGTTCAGGGGAAGAGGACGAG T G HOXB13 Ensembl:ENSG00000159184 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:48725254..48725378 26863196 MeRIP-seq:(Medium) rs945161120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6607993 97462 RMVar_ID_97462 Human_SNP_ID_626169421 m1A Human chr17 - 48725541 48725541 48725541 GTCGGTGGCGAGTAGTGGGGTCGGTGGCGAGCAGTTGGTGGTGGGCCGCGGCCGCCACTACCTCG GTCGGTGGCGAGTAGTGGGGTCGGTGGCGAGCGGTTGGTGGTGGGCCGCGGCCGCCACTACCTCG T C HOXB13 Ensembl:ENSG00000159184 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48725501..48725597 26863196 MeRIP-seq:(Medium) rs1439072047 Functional Loss SNV dbSNP153 33..33 33 - - - 97463 RMVar_ID_97463 Human_SNP_ID_626169720 m1A Human chr17 - 48726759 48726759 48726759 AAGAGATCTCCTTGCCTGGGTGGGAGGAGCGAAAGTGGGGGTGTCCTGGGGAGACCAGGAACCTG AAGAGATCTCCTTGCCTGGGTGGGAGGAGCGAGAGTGGGGGTGTCCTGGGGAGACCAGGAACCTG T C HOXB13 Ensembl:ENSG00000159184 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:48726708..48726809 26863196 MeRIP-seq:(Medium) rs1324591944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27256185 97464 RMVar_ID_97464 Human_SNP_ID_626204530 m1A Human chr17 - 48863296 48863296 48863296 TTAGTATCAAGTCAGGCCTGTTGTGAATACCCAGGTTGGCTCCATCCCAGGGCCCTTGTACTGAG TTAGTATCAAGTCAGGCCTGTTGTGAATACCCGGGTTGGCTCCATCCCAGGGCCCTTGTACTGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48863053..48863452 32194978 MeRIP-seq:(Medium) rs555768599 Functional Loss SNV dbSNP153 33..33 33 - - - 97465 RMVar_ID_97465 Human_SNP_ID_626212319 m1A Human chr17 - 48893404 48893404 48893404 ATGCCCCGGCGGTCTGCATTTTTTCAGTCTGCAGAGGGGGAAAAAATAGTAATAATAATCCCACT ATGCCCCGGCGGTCTGCATTTTTTCAGTCTGCGGAGGGGGAAAAAATAGTAATAATAATCCCACT T C SUMO2P17 Ensembl:ENSG00000248278 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr17:48893401..48893507;chr17:48893401..48893475 26863196,32194978 MeRIP-seq:(Medium) rs781541935 Functional Loss SNV dbSNP153 33..33 33 - - - 97466 RMVar_ID_97466 Human_SNP_ID_626212531 m1A Human chr17 + 48894340 48894340 48894340 GCTCAGCAATTAGGATTTTTTTTCCTTGACTGATTTGGTAGGATGTGGCTTTCTGATTTTACAGA GCTCAGCAATTAGGATTTTTTTTCCTTGACTGTTTTGGTAGGATGTGGCTTTCTGATTTTACAGA A T ATP5MC1 Ensembl:ENSG00000159199 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48894338..48894455 26863196 MeRIP-seq:(Medium) rs1434648873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13055637,Human_RBP_ID_22740555,Human_RBP_ID_23732669 RMVar_hsa_circ_99473,RMVar_hsa_circ_111164,RMVar_hsa_circ_185099,RMVar_hsa_circ_185100 97467 RMVar_ID_97467 Human_SNP_ID_626212729 m1A Human chr17 - 48895116 48895116 48895116 GAGAAGCAAGGCAGGCGAGATAGCAGAGAGATAGTATGGCATAAGGACAGGTGGCTGACTCTACC GAGAAGCAAGGCAGGCGAGATAGCAGAGAGATTGTATGGCATAAGGACAGGTGGCTGACTCTACC T A SUMO2P17 Ensembl:ENSG00000248278 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48895112..48895359 26863196 MeRIP-seq:(Medium) rs1567772309 Functional Loss SNV dbSNP153 33..33 33 - - - 97468 RMVar_ID_97468 Human_SNP_ID_626212806 m1A Human chr17 - 48895304 48895304 48895304 ACCTGGCATAGCCAATGATCAAGCTGCCAAACACGGTTCCAATGCCAGCCCCTGAACCAGCCACA ACCTGGCATAGCCAATGATCAAGCTGCCAAACGCGGTTCCAATGCCAGCCCCTGAACCAGCCACA T C SUMO2P17 Ensembl:ENSG00000248278 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:48895151..48895850;chr17:48895151..48895350 32194978 MeRIP-seq:(Medium) rs1483214161 Functional Loss SNV dbSNP153 33..33 33 - - - 97469 RMVar_ID_97469 Human_SNP_ID_626212914 m1A Human chr17 - 48895708 48895708 48895708 CCATCAAACAGAAAAGCCCCATGGCCTCAGACAGGGCAAAGCCAAGAATGGCATAGGAGAAGAGC CCATCAAACAGAAAAGCCCCATGGCCTCAGACGGGGCAAAGCCAAGAATGGCATAGGAGAAGAGC T C SUMO2P17 Ensembl:ENSG00000248278 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48895602..48895760 26863196 MeRIP-seq:(Medium) rs774757795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18701287 97470 RMVar_ID_97470 Human_SNP_ID_626216448 m1A Human chr17 + 48908448 48908448 48908448 CGGTTCTCGGTGGTGCGGGAGCGGGCGGGAGCAGCGGCCGCTCTGGTCGGCGGACGTGCTGCCGA CGGTTCTCGGTGGTGCGGGAGCGGGCGGGAGCCGCGGCCGCTCTGGTCGGCGGACGTGCTGCCGA A C UBE2Z Ensembl:ENSG00000159202 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:48908401..48908675;chr17:48908401..48908700;chr17:48908403..48908600 26863196 MeRIP-seq:(Medium) rs961503940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765765,Human_RBP_ID_4464647,Human_RBP_ID_23114475 RMVar_hsa_circ_100623,RMVar_hsa_circ_106892,RMVar_hsa_circ_185105,RMVar_hsa_circ_185106 97471 RMVar_ID_97471 Human_SNP_ID_626216777 m1A Human chr17 + 48909200 48909200 48909200 CGGCGCCGCCCCTATTTCCCCTTCCCCACCCCAACCTTGCTAGATGCTGCCCGCAGGCCCCACCC CGGCGCCGCCCCTATTTCCCCTTCCCCACCCCCACCTTGCTAGATGCTGCCCGCAGGCCCCACCC A C UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:48909081..48909228 26863196 MeRIP-seq:(Medium) rs1226860865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236499,Human_RBP_ID_5129194,Human_RBP_ID_17079641,Human_RBP_ID_18941823 RMVar_hsa_circ_100623,RMVar_hsa_circ_106892,RMVar_hsa_circ_185105,RMVar_hsa_circ_185106 97472 RMVar_ID_97472 Human_SNP_ID_626217870 m1A Human chr17 + 48912941 48912941 48912941 CCCGACTATCCCATCCACCCACCTCGGGTCAAACTGATGACAACGGGCAATAACACAGTGAGGTT CCCGACTATCCCATCCACCCACCTCGGGTCAAGCTGATGACAACGGGCAATAACACAGTGAGGTT A G UBE2Z Ensembl:ENSG00000159202 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48912920..48915768 32194978 MeRIP-seq:(Medium) rs764170901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48688,Human_RBP_ID_1536357,Human_RBP_ID_13055958,Human_RBP_ID_22216678 Human_Splice_Rec_1835105,Human_Splice_Rec_1835121,Human_Splice_Rec_1835131,Human_Splice_Rec_1835141 Human_miRNA_ID_268673 RMVar_hsa_circ_59442,RMVar_hsa_circ_100623,RMVar_hsa_circ_106892,RMVar_hsa_circ_110267,RMVar_hsa_circ_185105,RMVar_hsa_circ_185106,RMVar_hsa_circ_315581,RMVar_hsa_circ_58211,RMVar_hsa_circ_60229,RMVar_hsa_circ_185108,RMVar_hsa_circ_78664,RMVar_hsa_circ_185109,RMVar_hsa_circ_40946 97473 RMVar_ID_97473 Human_SNP_ID_626221910 m1A Human chr17 - 48927303 48927303 48927303 AGATGCTCCAGTGCCAAGGAGGTCAGACCGGGAACAGGCCCCCACTCCCACACCCTGGGATCGGA AGATGCTCCAGTGCCAAGGAGGTCAGACCGGGGACAGGCCCCCACTCCCACACCCTGGGATCGGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48927121..48927400 32194978 MeRIP-seq:(Medium) rs1462204145 Functional Loss SNV dbSNP153 33..33 33 - - - 97474 RMVar_ID_97474 Human_SNP_ID_626222221 m1A Human chr17 + 48928644 48928644 48928644 CAAAGGAGAATGTCCTATTTGGGAGGGCAGGAAGCAAAGGAACTGGACAGGGATTGGTGGGCTTG CAAAGGAGAATGTCCTATTTGGGAGGGCAGGAGGCAAAGGAACTGGACAGGGATTGGTGGGCTTG A G UBE2Z Ensembl:ENSG00000159202 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48928594..48928666 26863196 MeRIP-seq:(Medium) rs1003615964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236503,Human_RBP_ID_492677,Human_RBP_ID_820172,Human_RBP_ID_1008925,Human_RBP_ID_6608436,Human_RBP_ID_9866246,Human_RBP_ID_17895045,Human_RBP_ID_18293386,Human_RBP_ID_22953540,Human_RBP_ID_23118911 RMVar_hsa_circ_110267,RMVar_hsa_circ_185108,RMVar_hsa_circ_78664,RMVar_hsa_circ_109311,RMVar_hsa_circ_185109,RMVar_hsa_circ_185110,RMVar_hsa_circ_110992,RMVar_hsa_circ_185116,RMVar_hsa_circ_126567,RMVar_hsa_circ_185118,RMVar_hsa_circ_78837,RMVar_hsa_circ_185119 97475 RMVar_ID_97475 Human_SNP_ID_626222769 m1A Human chr17 - 48930512 48930510 48930513 GCCAGCTCTCTTCACTGACCTCTACTCCCAGGAGATTACAGCTGAGGAGGCCAGAGAAGCCCTCC GCCAGCTCTCTTCACTGACCTCTACTCCCAG___ATTACAGCTGAGGAGGCCAGAGAAGCCCTCC TCTC T SNF8 Ensembl:ENSG00000159210 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48930463..48930559 26863196 MeRIP-seq:(Medium) rs776117941 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_492696,Human_RBP_ID_17654259,Human_RBP_ID_26813774 97476 RMVar_ID_97476 Human_SNP_ID_626224555 m1A Human chr17 + 48936947 48936947 48936947 GTCCTTAGAGGCCTGTAGACTGCAGGATGGAAACGATAATCTTTTACGGTTTTCTCCCTCTCAGA GTCCTTAGAGGCCTGTAGACTGCAGGATGGAATCGATAATCTTTTACGGTTTTCTCCCTCTCAGA A T AC091133.1 Ensembl:ENSG00000230532 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48936946..48937047 32194978 MeRIP-seq:(Medium) rs996182216 Functional Loss SNV dbSNP153 33..33 33 - - - 97477 RMVar_ID_97477 Human_SNP_ID_626226633 m1A Human chr17 - 48943962 48943960 48943963 TGGTCTCTTTGTCTGACAGGCCAAGTATAAGGAGCGAGGGACGGTCTTGGCTGAGGACCAGCTAG TGGTCTCTTTGTCTGACAGGCCAAGTATAAG___CGAGGGACGGTCTTGGCTGAGGACCAGCTAG GCTC G SNF8 Ensembl:ENSG00000159210 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:48943926..48944000 26863196 MeRIP-seq:(Medium) rs1567791017 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_48701,Human_RBP_ID_236508,Human_RBP_ID_821980,Human_RBP_ID_905401,Human_RBP_ID_4466554,Human_RBP_ID_8232411,Human_RBP_ID_9376297,Human_RBP_ID_17654800,Human_RBP_ID_22959235 Human_Splice_Rec_1835158,Human_Splice_Rec_1835159,Human_Splice_Rec_1835172,Human_Splice_Rec_1835173,Human_Splice_Rec_1835180,Human_Splice_Rec_1835181,Human_Splice_Rec_1835196,Human_Splice_Rec_1835197,Human_Splice_Rec_1835232,Human_Splice_Rec_1835233,Human_Splice_Rec_1835240,Human_Splice_Rec_1835241,Human_Splice_Rec_1835252,Human_Splice_Rec_1835253,Human_Splice_Rec_1835268,Human_Splice_Rec_1835269,Human_Splice_Rec_1835280,Human_Splice_Rec_1835281,Human_Splice_Rec_1835291,Human_Splice_Rec_1835296,Human_Splice_Rec_1835297 RMVar_hsa_circ_91459,RMVar_hsa_circ_307842,RMVar_hsa_circ_185121,RMVar_hsa_circ_185122 97478 RMVar_ID_97478 Human_SNP_ID_626226639 m1A Human chr17 - 48943977 48943977 48943977 TCTCTTAACTTATGCTGGTCTCTTTGTCTGACAGGCCAAGTATAAGGAGCGAGGGACGGTCTTGG TCTCTTAACTTATGCTGGTCTCTTTGTCTGACCGGCCAAGTATAAGGAGCGAGGGACGGTCTTGG T G SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:48943878..48944032;chr17:48943926..48944085;chr17:48943926..48944092;chr17:48943926..48944000;chr17:48943926..48944029;chr17:48940976..48944029 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1455420117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8232411,Human_RBP_ID_8455800,Human_RBP_ID_17654800,Human_RBP_ID_22656511 Human_Splice_Rec_1835159,Human_Splice_Rec_1835173,Human_Splice_Rec_1835181,Human_Splice_Rec_1835197,Human_Splice_Rec_1835233,Human_Splice_Rec_1835241,Human_Splice_Rec_1835253,Human_Splice_Rec_1835269,Human_Splice_Rec_1835281,Human_Splice_Rec_1835291,Human_Splice_Rec_1835297 97479 RMVar_ID_97479 Human_SNP_ID_626226852 m1A Human chr17 - 48944690 48944690 48944690 GGGGTGGGAGCTGGCGCCATCGCCAAGAAGAAACTTGCAGAGGTGAGCAGGAAGAAGGCCGACCC GGGGTGGGAGCTGGCGCCATCGCCAAGAAGAAGCTTGCAGAGGTGAGCAGGAAGAAGGCCGACCC T C SNF8 Ensembl:ENSG00000159210 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:48944676..48944800 26863410 MeRIP-seq:(Medium) rs1490699271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4436122,Human_RBP_ID_5115555,Human_RBP_ID_5143283,Human_RBP_ID_5318469,Human_RBP_ID_5367380,Human_RBP_ID_9353321,Human_RBP_ID_9376299,Human_RBP_ID_18419644,Human_RBP_ID_18470076,Human_RBP_ID_19083104,Human_RBP_ID_22061492,Human_RBP_ID_24545024,Human_RBP_ID_26965245 Human_Splice_Rec_1835157,Human_Splice_Rec_1835171,Human_Splice_Rec_1835179,Human_Splice_Rec_1835195,Human_Splice_Rec_1835231,Human_Splice_Rec_1835239,Human_Splice_Rec_1835251,Human_Splice_Rec_1835267,Human_Splice_Rec_1835279,Human_Splice_Rec_1835295 97480 RMVar_ID_97480 Human_SNP_ID_626226864 m1A Human chr17 + 48944739 48944739 48944739 CGCCAGCTCCCACCCCGCGGCGGTGCATCCCCACCCTGGGCCCGCGGGCCGCCCGGCTGCCGGGA CGCCAGCTCCCACCCCGCGGCGGTGCATCCCCCCCCTGGGCCCGCGGGCCGCCCGGCTGCCGGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48944128..48944769 32194978 MeRIP-seq:(Medium) rs780254745 Functional Loss SNV dbSNP153 33..33 33 - - - 97481 RMVar_ID_97481 Human_SNP_ID_626226868 m1A Human chr17 - 48944743 48944743 48944743 GGGGTCCCGGCAGCCGGGCGGCCCGCGGGCCCAGGGTGGGGATGCACCGCCGCGGGGTGGGAGCT GGGGTCCCGGCAGCCGGGCGGCCCGCGGGCCCGGGGTGGGGATGCACCGCCGCGGGGTGGGAGCT T C SNF8 Ensembl:ENSG00000159210 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:48944676..48944794 26863410 MeRIP-seq:(Medium) rs767974351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237963,Human_RBP_ID_3952642,Human_RBP_ID_4436124,Human_RBP_ID_5114747,Human_RBP_ID_5143283,Human_RBP_ID_5318469,Human_RBP_ID_9353321,Human_RBP_ID_9378471,Human_RBP_ID_18419646,Human_RBP_ID_18470076,Human_RBP_ID_21890186,Human_RBP_ID_24545024,Human_RBP_ID_26769549 Human_Splice_Rec_1835157,Human_Splice_Rec_1835171,Human_Splice_Rec_1835179,Human_Splice_Rec_1835195,Human_Splice_Rec_1835231,Human_Splice_Rec_1835239,Human_Splice_Rec_1835251,Human_Splice_Rec_1835267,Human_Splice_Rec_1835279,Human_Splice_Rec_1835295 97482 RMVar_ID_97482 Human_SNP_ID_626226901 m1A Human chr17 - 48944779 48944779 48944779 GGGGAGCCGGCGGCGGAGTCCGGGACGTGGAGACCCGGGGTCCCGGCAGCCGGGCGGCCCGCGGG GGGGAGCCGGCGGCGGAGTCCGGGACGTGGAGTCCCGGGGTCCCGGCAGCCGGGCGGCCCGCGGG T A SNF8 Ensembl:ENSG00000159210 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:48944128..48944850;chr17:48944658..48944825;chr17:48944128..48944868;chr17:48944624..48944850;chr17:48944671..48944850 26863196 MeRIP-seq:(Medium) rs1028669996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237963,Human_RBP_ID_767187,Human_RBP_ID_4464649,Human_RBP_ID_5143283,Human_RBP_ID_5318469,Human_RBP_ID_5367381,Human_RBP_ID_9353321,Human_RBP_ID_18419646,Human_RBP_ID_21890186,Human_RBP_ID_26769549 Human_Splice_Rec_1835157,Human_Splice_Rec_1835171,Human_Splice_Rec_1835179,Human_Splice_Rec_1835195,Human_Splice_Rec_1835231,Human_Splice_Rec_1835239,Human_Splice_Rec_1835251,Human_Splice_Rec_1835267,Human_Splice_Rec_1835279,Human_Splice_Rec_1835295 97483 RMVar_ID_97483 Human_SNP_ID_626226905 m1A Human chr17 + 48944784 48944784 48944784 GGGCCGCCCGGCTGCCGGGACCCCGGGTCTCCACGTCCCGGACTCCGCCGCCGGCTCCCCAAGGC GGGCCGCCCGGCTGCCGGGACCCCGGGTCTCCTCGTCCCGGACTCCGCCGCCGGCTCCCCAAGGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:48944659..48944827;chr17:48944659..48944825 26863196 MeRIP-seq:(Medium) rs954394804 Functional Loss SNV dbSNP153 33..33 33 - - - 97484 RMVar_ID_97484 Human_SNP_ID_626241228 m1A Human chr17 + 48997531 48997531 48997531 CCGTGTCGTCCGTCTCCCTGCGCGCCGCGGGCACTTCTCCTGGGCTCTCCCCGAACTCTCCCGCG CCGTGTCGTCCGTCTCCCTGCGCGCCGCGGGCTCTTCTCCTGGGCTCTCCCCGAACTCTCCCGCG A T IGF2BP1 Ensembl:ENSG00000159217 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:48997480..48997718 26863196 MeRIP-seq:(Medium) rs925805068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236509,Human_RBP_ID_492739,Human_RBP_ID_4436145,Human_RBP_ID_5420210,Human_RBP_ID_5441587,Human_RBP_ID_5466644,Human_RBP_ID_5497263,Human_RBP_ID_8819199,Human_RBP_ID_9326730,Human_RBP_ID_13056913,Human_RBP_ID_17260461,Human_RBP_ID_18701364,Human_RBP_ID_22061493,Human_RBP_ID_22443773,Human_RBP_ID_27454015 Human_miRNA_ID_2994922 RMVar_hsa_circ_86147,RMVar_hsa_circ_185123 97485 RMVar_ID_97485 Human_SNP_ID_626241277 m1A Human chr17 - 48997704 48997704 48997704 CTCGGGGCAGGACGCGGTCCCGGGCAAGGCCGAACGAGCGGGCGCGGGCGGCGAGCCTCCTAGGC CTCGGGGCAGGACGCGGTCCCGGGCAAGGCCGGACGAGCGGGCGCGGGCGGCGAGCCTCCTAGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:48997501..48997800 26863410 MeRIP-seq:(Medium) rs1265656113 Functional Loss SNV dbSNP153 33..33 33 - - - 97486 RMVar_ID_97486 Human_SNP_ID_626241281 m1A Human chr17 - 48997711 48997711 48997711 TGGCGGTCTCGGGGCAGGACGCGGTCCCGGGCAAGGCCGAACGAGCGGGCGCGGGCGGCGAGCCT TGGCGGTCTCGGGGCAGGACGCGGTCCCGGGCTAGGCCGAACGAGCGGGCGCGGGCGGCGAGCCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48997511..48997711 32194978 MeRIP-seq:(Medium) rs903925615 Functional Loss SNV dbSNP153 33..33 33 - - - 97487 RMVar_ID_97487 Human_SNP_ID_626241282 m1A Human chr17 - 48997711 48997711 48997711 TGGCGGTCTCGGGGCAGGACGCGGTCCCGGGCAAGGCCGAACGAGCGGGCGCGGGCGGCGAGCCT TGGCGGTCTCGGGGCAGGACGCGGTCCCGGGCGAGGCCGAACGAGCGGGCGCGGGCGGCGAGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48997511..48997711 32194978 MeRIP-seq:(Medium) rs903925615 Functional Loss SNV dbSNP153 33..33 33 - - - 97488 RMVar_ID_97488 Human_SNP_ID_626241677 m1A Human chr17 + 48998707 48998707 48998707 AGCCCGTCTTCCTGGCCAACAGAGAAAAATAAAGTTTCATTCTGCACACTGCCTCCCGCCCCGCG AGCCCGTCTTCCTGGCCAACAGAGAAAAATAAGGTTTCATTCTGCACACTGCCTCCCGCCCCGCG A G IGF2BP1 Ensembl:ENSG00000159217 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48998704..48998833 26863196 MeRIP-seq:(Medium) rs1425159670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8455809 RMVar_hsa_circ_86147,RMVar_hsa_circ_185123 97489 RMVar_ID_97489 Human_SNP_ID_626252828 m1A Human chr17 + 49038241 49038241 49038241 CCCTGAAGGTCTCCTACATCCCCGATGAGCAGATAGCACAGGGACCTGAGAATGGGCGCCGAGGG CCCTGAAGGTCTCCTACATCCCCGATGAGCAGGTAGCACAGGGACCTGAGAATGGGCGCCGAGGG A G IGF2BP1 Ensembl:ENSG00000159217 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:49038190..49038390 32194978 MeRIP-seq:(Medium) rs1429710029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536432,Human_RBP_ID_3950834,Human_RBP_ID_4436184,Human_RBP_ID_6608787,Human_RBP_ID_9290196,Human_RBP_ID_9376301,Human_RBP_ID_13057702,Human_RBP_ID_17260473,Human_RBP_ID_26332025 Human_Splice_Rec_1835328,Human_Splice_Rec_1835396 RMVar_hsa_circ_3488,RMVar_hsa_circ_11173,RMVar_hsa_circ_104939,RMVar_hsa_circ_86147,RMVar_hsa_circ_185123,RMVar_hsa_circ_185124,RMVar_hsa_circ_370207,RMVar_hsa_circ_76622,RMVar_hsa_circ_185125,RMVar_hsa_circ_185128,RMVar_hsa_circ_92889,RMVar_hsa_circ_377817,RMVar_hsa_circ_10829,RMVar_hsa_circ_51224,RMVar_hsa_circ_113312,RMVar_hsa_circ_185129,RMVar_hsa_circ_340159,RMVar_hsa_circ_45562,RMVar_hsa_circ_185130 97490 RMVar_ID_97490 Human_SNP_ID_626291839 m1A Human chr17 - 49193423 49193423 49193423 TTTCTCTGTCTCCCAGGCTGGAGTACACAGGCACGATCTCGGCTCACTGCAACCTCCACTTCCCG TTTCTCTGTCTCCCAGGCTGGAGTACACAGGCGCGATCTCGGCTCACTGCAACCTCCACTTCCCG T C lnc-GNGT2-1-001 RNACentral:URS0000D5B030 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:49193377..49193461 26863196 MeRIP-seq:(Medium) rs1219724608 Functional Loss SNV dbSNP153 33..33 33 - - - 97491 RMVar_ID_97491 Human_SNP_ID_626323834 m1A Human chr17 - 49317086 49317086 49317086 CTTCCCCTACTCCCAGAACTACAAGAGGTCGTAGGAAGAGTGTAGAGCCACCTAAGCGTAAGAAG CTTCCCCTACTCCCAGAACTACAAGAGGTCGTGGGAAGAGTGTAGAGCCACCTAAGCGTAAGAAG T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:49317036..49317128 26863196 MeRIP-seq:(Medium) rs1248677421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49718,Human_RBP_ID_902995,Human_RBP_ID_8819478,Human_RBP_ID_9378482,Human_RBP_ID_13058691,Human_RBP_ID_24544888 RMVar_hsa_circ_343496,RMVar_hsa_circ_67126,RMVar_hsa_circ_185155,RMVar_hsa_circ_295581,RMVar_hsa_circ_270757,RMVar_hsa_circ_185152,RMVar_hsa_circ_185153,RMVar_hsa_circ_360255,RMVar_hsa_circ_18262,RMVar_hsa_circ_351389,RMVar_hsa_circ_283857,RMVar_hsa_circ_185156,RMVar_hsa_circ_185158,RMVar_hsa_circ_185159,RMVar_hsa_circ_327123 97492 RMVar_ID_97492 Human_SNP_ID_626323848 m1A Human chr17 - 49317110 49317110 49317110 CTGCCTCTGTTGCCGCAGCTACCACTTCCCCTACTCCCAGAACTACAAGAGGTCGTAGGAAGAGT CTGCCTCTGTTGCCGCAGCTACCACTTCCCCTGCTCCCAGAACTACAAGAGGTCGTAGGAAGAGT T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:49317060..49317311 26863196 MeRIP-seq:(Medium) rs199551437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49718,Human_RBP_ID_898612,Human_RBP_ID_22061501,Human_RBP_ID_24544888,Human_RBP_ID_26332037,Human_RBP_ID_27814027 RMVar_hsa_circ_343496,RMVar_hsa_circ_67126,RMVar_hsa_circ_185155,RMVar_hsa_circ_295581,RMVar_hsa_circ_270757,RMVar_hsa_circ_185152,RMVar_hsa_circ_185153,RMVar_hsa_circ_360255,RMVar_hsa_circ_18262,RMVar_hsa_circ_351389,RMVar_hsa_circ_283857,RMVar_hsa_circ_185156,RMVar_hsa_circ_185158,RMVar_hsa_circ_185159,RMVar_hsa_circ_327123,RMVar_hsa_circ_185160 97493 RMVar_ID_97493 Human_SNP_ID_626323875 m1A Human chr17 - 49317190 49317188 49317191 CTATGGAGAGAATGAAAAGCAGAAGAAAAAGGAGAAGATAGTAGAGAAAGTCAGCGTTACACAAA CTATGGAGAGAATGAAAAGCAGAAGAAAAAG___AAGATAGTAGAGAAAGTCAGCGTTACACAAA TCTC T ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:49317050..49317273 26863196 MeRIP-seq:(Medium) rs746401797 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_898612,Human_RBP_ID_24544888,Human_RBP_ID_26332037,Human_RBP_ID_27814027 RMVar_hsa_circ_343496,RMVar_hsa_circ_67126,RMVar_hsa_circ_185155,RMVar_hsa_circ_295581,RMVar_hsa_circ_270757,RMVar_hsa_circ_185152,RMVar_hsa_circ_185153,RMVar_hsa_circ_360255,RMVar_hsa_circ_18262,RMVar_hsa_circ_351389,RMVar_hsa_circ_283857,RMVar_hsa_circ_185156,RMVar_hsa_circ_185158,RMVar_hsa_circ_185159,RMVar_hsa_circ_327123,RMVar_hsa_circ_185160 97494 RMVar_ID_97494 Human_SNP_ID_626335828 m1A Human chr17 - 49362040 49362040 49362040 AGGCCGGGTCTGAGGAGCGGCCCTGAGGACAGACGTTGGGCAGGGGGGGAGGGGCTGGCCCAGCC AGGCCGGGTCTGAGGAGCGGCCCTGAGGACAGGCGTTGGGCAGGGGGGGAGGGGCTGGCCCAGCC T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49361843..49362205 26863196 MeRIP-seq:(Medium) rs1266656031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238313,Human_RBP_ID_492953,Human_RBP_ID_4436656,Human_RBP_ID_5237921 97495 RMVar_ID_97495 Human_SNP_ID_626347149 m1A Human chr17 - 49409087 49409087 49409087 CTGGTCTCCAGGCAGGTGAGCGACGACCTTACAGAGCGAGCCGCCACCTTTGGGCTCATCCTGGA CTGGTCTCCAGGCAGGTGAGCGACGACCTTACGGAGCGAGCCGCCACCTTTGGGCTCATCCTGGA T C PHB Ensembl:ENSG00000167085 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:49409026..49411852 32194978 MeRIP-seq:(Medium) rs756098528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492978,Human_RBP_ID_821223,Human_RBP_ID_903584,Human_RBP_ID_1861835,Human_RBP_ID_5114750,Human_RBP_ID_17260557,Human_RBP_ID_17895311,Human_RBP_ID_18190895,Human_RBP_ID_22445587,Human_RBP_ID_22760850 Human_Splice_Rec_1835736,Human_Splice_Rec_1835737,Human_Splice_Rec_1835750,Human_Splice_Rec_1835751,Human_Splice_Rec_1835762,Human_Splice_Rec_1835770,Human_Splice_Rec_1835771,Human_Splice_Rec_1835786,Human_Splice_Rec_1835787,Human_Splice_Rec_1835798,Human_Splice_Rec_1835799,Human_Splice_Rec_1835806,Human_Splice_Rec_1835807,Human_Splice_Rec_1835816,Human_Splice_Rec_1835817,Human_Splice_Rec_1835826,Human_Splice_Rec_1835827,Human_Splice_Rec_1835836,Human_Splice_Rec_1835842 RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_104434,RMVar_hsa_circ_90200,RMVar_hsa_circ_185164,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185165,RMVar_hsa_circ_110940,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225,RMVar_hsa_circ_375013,RMVar_hsa_circ_185168,RMVar_hsa_circ_376357,RMVar_hsa_circ_185170,RMVar_hsa_circ_185171 97496 RMVar_ID_97496 Human_SNP_ID_626347152 m1A Human chr17 + 49409090 49409090 49409090 AGGATGAGCCCAAAGGTGGCGGCTCGCTCTGTAAGGTCGTCGCTCACCTGCCTGGAGACCAGCTC AGGATGAGCCCAAAGGTGGCGGCTCGCTCTGTGAGGTCGTCGCTCACCTGCCTGGAGACCAGCTC A G AC091180.6 Ensembl:ENSG00000262039 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:49409029..49409100;chr17:49409026..49409175 26863196,32194978 MeRIP-seq:(Medium) rs1447226472 Functional Loss SNV dbSNP153 33..33 33 - - - 97497 RMVar_ID_97497 Human_SNP_ID_626347824 m1A Human chr17 - 49411743 49411743 49411743 GGAAGGGACTCATTTTCTCATCCCGTGGGTACAGAAACCAATTATCTTTGACTGCCGTTCTCGAC GGAAGGGACTCATTTTCTCATCCCGTGGGTACGGAAACCAATTATCTTTGACTGCCGTTCTCGAC T C PHB Ensembl:ENSG00000167085 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746659527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492981,Human_RBP_ID_3527393,Human_RBP_ID_4436726,Human_RBP_ID_9073244,Human_RBP_ID_17260560,Human_RBP_ID_17895313,Human_RBP_ID_18701520,Human_RBP_ID_22444745,Human_RBP_ID_26812550,Human_RBP_ID_27454113 Human_Splice_Rec_1835732,Human_Splice_Rec_1835733,Human_Splice_Rec_1835746,Human_Splice_Rec_1835747,Human_Splice_Rec_1835758,Human_Splice_Rec_1835759,Human_Splice_Rec_1835766,Human_Splice_Rec_1835767,Human_Splice_Rec_1835782,Human_Splice_Rec_1835783,Human_Splice_Rec_1835794,Human_Splice_Rec_1835795,Human_Splice_Rec_1835812,Human_Splice_Rec_1835813,Human_Splice_Rec_1835822,Human_Splice_Rec_1835823,Human_Splice_Rec_1835832,Human_Splice_Rec_1835833,Human_Splice_Rec_1835838,Human_Splice_Rec_1835839,Human_Splice_Rec_1835846,Human_Splice_Rec_1835847,Human_Splice_Rec_1835849 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_90200,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185165,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97498 RMVar_ID_97498 Human_SNP_ID_626347825 m1A Human chr17 - 49411743 49411743 49411743 GGAAGGGACTCATTTTCTCATCCCGTGGGTACAGAAACCAATTATCTTTGACTGCCGTTCTCGAC GGAAGGGACTCATTTTCTCATCCCGTGGGTACCGAAACCAATTATCTTTGACTGCCGTTCTCGAC T G PHB Ensembl:ENSG00000167085 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746659527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492981,Human_RBP_ID_3527393,Human_RBP_ID_4436726,Human_RBP_ID_9073244,Human_RBP_ID_17260560,Human_RBP_ID_17895313,Human_RBP_ID_18701520,Human_RBP_ID_22444745,Human_RBP_ID_26812550,Human_RBP_ID_27454113 Human_Splice_Rec_1835732,Human_Splice_Rec_1835733,Human_Splice_Rec_1835746,Human_Splice_Rec_1835747,Human_Splice_Rec_1835758,Human_Splice_Rec_1835759,Human_Splice_Rec_1835766,Human_Splice_Rec_1835767,Human_Splice_Rec_1835782,Human_Splice_Rec_1835783,Human_Splice_Rec_1835794,Human_Splice_Rec_1835795,Human_Splice_Rec_1835812,Human_Splice_Rec_1835813,Human_Splice_Rec_1835822,Human_Splice_Rec_1835823,Human_Splice_Rec_1835832,Human_Splice_Rec_1835833,Human_Splice_Rec_1835838,Human_Splice_Rec_1835839,Human_Splice_Rec_1835846,Human_Splice_Rec_1835847,Human_Splice_Rec_1835849 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_90200,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185165,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97499 RMVar_ID_97499 Human_SNP_ID_626347844 m1A Human chr17 - 49411791 49411791 49411791 AGCTGTCATCTTTGACCGATTCCGTGGAGTGCAGGACATTGTGGTAGGGGAAGGGACTCATTTTC AGCTGTCATCTTTGACCGATTCCGTGGAGTGCCGGACATTGTGGTAGGGGAAGGGACTCATTTTC T G PHB Ensembl:ENSG00000167085 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr17:49411640..49411902;chr17:49409326..49411852 26863196,32194978 MeRIP-seq:(Medium) rs1456528524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_492982,Human_RBP_ID_765899,Human_RBP_ID_1182733,Human_RBP_ID_1536531,Human_RBP_ID_1861839,Human_RBP_ID_3527394,Human_RBP_ID_4466563,Human_RBP_ID_6609549,Human_RBP_ID_8455960,Human_RBP_ID_13059576,Human_RBP_ID_17260560,Human_RBP_ID_17492099,Human_RBP_ID_17895314,Human_RBP_ID_18701521,Human_RBP_ID_22443780,Human_RBP_ID_22761591,Human_RBP_ID_23210029,Human_RBP_ID_23733246,Human_RBP_ID_26812551,Human_RBP_ID_27454113 Human_Splice_Rec_1835732,Human_Splice_Rec_1835746,Human_Splice_Rec_1835758,Human_Splice_Rec_1835766,Human_Splice_Rec_1835782,Human_Splice_Rec_1835794,Human_Splice_Rec_1835812,Human_Splice_Rec_1835822,Human_Splice_Rec_1835832,Human_Splice_Rec_1835838,Human_Splice_Rec_1835846 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_90200,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185165,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97500 RMVar_ID_97500 Human_SNP_ID_626348148 m1A Human chr17 + 49413230 49413230 49413230 CCACGCCTCCTGCAACAGCTAAGGCCAGGCCAAACTTGCCAATGGACTCAAACACTTTGGCAGCC CCACGCCTCCTGCAACAGCTAAGGCCAGGCCAGACTTGCCAATGGACTCAAACACTTTGGCAGCC A G AC091180.6 Ensembl:ENSG00000262039 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:49413176..49413336 26863410 MeRIP-seq:(Medium) rs902509386 Functional Loss SNV dbSNP153 33..33 33 - - - 97501 RMVar_ID_97501 Human_SNP_ID_626348161 m1A Human chr17 - 49413266 49413266 49413266 CCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAACATGGCTGCCAAAGTGTTTGAGTCCATTGGCA CCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAGCATGGCTGCCAAAGTGTTTGAGTCCATTGGCA T C PHB Ensembl:ENSG00000167085 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:49413132..49414900;chr17:49413148..49414905 26863196 MeRIP-seq:(Medium) rs1466781755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236573,Human_RBP_ID_903588,Human_RBP_ID_4466565,Human_RBP_ID_5114751,Human_RBP_ID_5364541,Human_RBP_ID_9327351,Human_RBP_ID_17654261,Human_RBP_ID_22445593,Human_RBP_ID_23210031 Human_Splice_Rec_1835730,Human_Splice_Rec_1835731,Human_Splice_Rec_1835744,Human_Splice_Rec_1835745,Human_Splice_Rec_1835756,Human_Splice_Rec_1835757,Human_Splice_Rec_1835764,Human_Splice_Rec_1835765,Human_Splice_Rec_1835780,Human_Splice_Rec_1835781,Human_Splice_Rec_1835792,Human_Splice_Rec_1835793,Human_Splice_Rec_1835803,Human_Splice_Rec_1835811,Human_Splice_Rec_1835820,Human_Splice_Rec_1835821,Human_Splice_Rec_1835830,Human_Splice_Rec_1835831,Human_Splice_Rec_1835844,Human_Splice_Rec_1835845,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97502 RMVar_ID_97502 Human_SNP_ID_626348162 m1A Human chr17 - 49413267 49413267 49413267 CCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAACATGGCTGCCAAAGTGTTTGAGTCCATTGGC CCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAGACATGGCTGCCAAAGTGTTTGAGTCCATTGGC T C PHB Ensembl:ENSG00000167085 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49413144..49414875 26863196 MeRIP-seq:(Medium) rs777684351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236573,Human_RBP_ID_903588,Human_RBP_ID_4466565,Human_RBP_ID_5114751,Human_RBP_ID_5364541,Human_RBP_ID_9327351,Human_RBP_ID_17654261,Human_RBP_ID_22445593,Human_RBP_ID_23210031 Human_Splice_Rec_1835730,Human_Splice_Rec_1835731,Human_Splice_Rec_1835744,Human_Splice_Rec_1835745,Human_Splice_Rec_1835756,Human_Splice_Rec_1835757,Human_Splice_Rec_1835764,Human_Splice_Rec_1835765,Human_Splice_Rec_1835780,Human_Splice_Rec_1835781,Human_Splice_Rec_1835792,Human_Splice_Rec_1835793,Human_Splice_Rec_1835803,Human_Splice_Rec_1835811,Human_Splice_Rec_1835820,Human_Splice_Rec_1835821,Human_Splice_Rec_1835830,Human_Splice_Rec_1835831,Human_Splice_Rec_1835844,Human_Splice_Rec_1835845,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97503 RMVar_ID_97503 Human_SNP_ID_626348166 m1A Human chr17 - 49413277 49413277 49413277 TTGTTTTTATCCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAACATGGCTGCCAAAGTGTTTGA TTGTTTTTATCCCCTTAGGTGTGAGAGGGTCCGGCAGAAGGAAACATGGCTGCCAAAGTGTTTGA T C PHB Ensembl:ENSG00000167085 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:49413226..49413300 32194978 MeRIP-seq:(Medium) rs749139558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236573,Human_RBP_ID_821226,Human_RBP_ID_903588,Human_RBP_ID_4466565,Human_RBP_ID_5114751,Human_RBP_ID_5364541,Human_RBP_ID_9327351,Human_RBP_ID_17654261,Human_RBP_ID_22444747,Human_RBP_ID_23210031 Human_Splice_Rec_1835730,Human_Splice_Rec_1835744,Human_Splice_Rec_1835756,Human_Splice_Rec_1835764,Human_Splice_Rec_1835780,Human_Splice_Rec_1835792,Human_Splice_Rec_1835820,Human_Splice_Rec_1835830,Human_Splice_Rec_1835844,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 97504 RMVar_ID_97504 Human_SNP_ID_626389823 m1A Human chr17 - 49576071 49576071 49576071 CGGCCCTCCCCTCAGCGGGTCGCCCAGGGCCGACCCCGCCCCCTTCGGTCCAGCTGTGCAGCCGC CGGCCCTCCCCTCAGCGGGTCGCCCAGGGCCGCCCCCGCCCCCTTCGGTCCAGCTGTGCAGCCGC T G AC006487.2 Ensembl:ENSG00000250310 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:49575928..49576139 26863196 MeRIP-seq:(Medium) rs1335658996 Functional Loss SNV dbSNP153 33..33 33 - - - 97505 RMVar_ID_97505 Human_SNP_ID_626400419 m1A Human chr17 + 49622855 49622855 49622855 GGTTAAACGAGATTTCCAAAGTCAGGGGGCAAAGATTTCTGTTCCCTCTTCACCCTGGTCAGATC GGTTAAACGAGATTTCCAAAGTCAGGGGGCAAGGATTTCTGTTCCCTCTTCACCCTGGTCAGATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:49622804..49636259 26863196 MeRIP-seq:(Medium) rs1004573148 Functional Loss SNV dbSNP153 33..33 33 - - - 97506 RMVar_ID_97506 Human_SNP_ID_626413185 m1A Human chr17 + 49677886 49677886 49677886 CAGTCACCTCTTCAGGGAGGTGCCCCCCCCCCACTCCGACAGGACAACCCCCTCCCTCGACTCTC CAGTCACCTCTTCAGGGAGGTGCCCCCCCCCCCCTCCGACAGGACAACCCCCTCCCTCGACTCTC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:49677883..49678025 26863410 MeRIP-seq:(Medium) rs905107313 Functional Loss SNV dbSNP153 33..33 33 - - - 97507 RMVar_ID_97507 Human_SNP_ID_626418914 m1A Human chr17 + 49701441 49701441 49701441 TTGAGATAATAACTTAAATATTCTTGATGTGGAGGTAGTCTCTCTCTTCCTAGTGGGATGTCTTC TTGAGATAATAACTTAAATATTCTTGATGTGGGGGTAGTCTCTCTCTTCCTAGTGGGATGTCTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49701390..49701540 32194978 MeRIP-seq:(Medium) rs112437889 Functional Loss SNV dbSNP153 33..33 33 - - - 97508 RMVar_ID_97508 Human_SNP_ID_626418915 m1A Human chr17 + 49701441 49701441 49701441 TTGAGATAATAACTTAAATATTCTTGATGTGGAGGTAGTCTCTCTCTTCCTAGTGGGATGTCTTC TTGAGATAATAACTTAAATATTCTTGATGTGGTGGTAGTCTCTCTCTTCCTAGTGGGATGTCTTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49701390..49701540 32194978 MeRIP-seq:(Medium) rs112437889 Functional Loss SNV dbSNP153 33..33 33 - - - 97509 RMVar_ID_97509 Human_SNP_ID_626419354 m1A Human chr17 + 49703008 49703008 49703008 GGGACCAAAATACACAACCGTCATAAAGATGAAGCTCTAGAGAAAGATAAAGGTGAGGTCCGGTG GGGACCAAAATACACAACCGTCATAAAGATGAGGCTCTAGAGAAAGATAAAGGTGAGGTCCGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49702882..49703032 32194978 MeRIP-seq:(Medium) rs1390373059 Functional Loss SNV dbSNP153 33..33 33 - - - 97510 RMVar_ID_97510 Human_SNP_ID_626419661 m1A Human chr17 - 49704129 49704129 49704129 AACAGGCTCCAACCACATGATGCTGAACATCAACCTTTGGTCGACATTGCTGCTGGGAATGGGTG AACAGGCTCCAACCACATGATGCTGAACATCAGCCTTTGGTCGACATTGCTGCTGGGAATGGGTG T C SLC35B1 Ensembl:ENSG00000121073 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49704124..49705318 32194978 MeRIP-seq:(Medium) rs1277101025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896686,Human_RBP_ID_1182757,Human_RBP_ID_1861946,Human_RBP_ID_3527507,Human_RBP_ID_5497284,Human_RBP_ID_8456043,Human_RBP_ID_23733479,Human_RBP_ID_26812557 Human_Splice_Rec_1836228,Human_Splice_Rec_1836229,Human_Splice_Rec_1836244,Human_Splice_Rec_1836245,Human_Splice_Rec_1836256,Human_Splice_Rec_1836257,Human_Splice_Rec_1836274,Human_Splice_Rec_1836275,Human_Splice_Rec_1836294,Human_Splice_Rec_1836295,Human_Splice_Rec_1836312,Human_Splice_Rec_1836313,Human_Splice_Rec_1836328,Human_Splice_Rec_1836329,Human_Splice_Rec_1836336,Human_Splice_Rec_1836337,Human_Splice_Rec_1836340,Human_Splice_Rec_1836350,Human_Splice_Rec_1836360,Human_Splice_Rec_1836372,Human_Splice_Rec_1836380 Human_miRNA_ID_2113943,Human_miRNA_ID_2597744 RMVar_hsa_circ_24302,RMVar_hsa_circ_122402,RMVar_hsa_circ_24075,RMVar_hsa_circ_185176,RMVar_hsa_circ_51591,RMVar_hsa_circ_7034,RMVar_hsa_circ_63795 97511 RMVar_ID_97511 Human_SNP_ID_626420769 m1A Human chr17 + 49707757 49707757 49707757 CTCACATCTTTTCCTGCAGGATCCCATAGTAAAAATAGCAGACAAAGACACCCAGGAAGCAGAGC CTCACATCTTTTCCTGCAGGATCCCATAGTAAGAATAGCAGACAAAGACACCCAGGAAGCAGAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49707749..49707849 32194978 MeRIP-seq:(Medium) rs778142334 Functional Loss SNV dbSNP153 33..33 33 - - - 97512 RMVar_ID_97512 Human_SNP_ID_626433452 m1A Human chr17 - 49764087 49764087 49764087 CAGTGGGGCTGAGGCAGGCAGCCGGGAGAGCCATGGCGGGGGCCGCAGCGGGCGGCAGAGGCGGA CAGTGGGGCTGAGGCAGGCAGCCGGGAGAGCCTTGGCGGGGGCCGCAGCGGGCGGCAGAGGCGGA T A FAM117A Ensembl:ENSG00000121104 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:49747249..49764142 26863196 MeRIP-seq:(Medium) rs749925224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237754,Human_RBP_ID_768390,Human_RBP_ID_3543040,Human_RBP_ID_4436889,Human_RBP_ID_18419648 97513 RMVar_ID_97513 Human_SNP_ID_626433453 m1A Human chr17 - 49764087 49764087 49764087 CAGTGGGGCTGAGGCAGGCAGCCGGGAGAGCCATGGCGGGGGCCGCAGCGGGCGGCAGAGGCGGA CAGTGGGGCTGAGGCAGGCAGCCGGGAGAGCCGTGGCGGGGGCCGCAGCGGGCGGCAGAGGCGGA T C FAM117A Ensembl:ENSG00000121104 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:49747249..49764142 26863196 MeRIP-seq:(Medium) rs749925224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237754,Human_RBP_ID_768390,Human_RBP_ID_3543040,Human_RBP_ID_4436889,Human_RBP_ID_18419648 97514 RMVar_ID_97514 Human_SNP_ID_626433487 m1A Human chr17 + 49764132 49764132 49764132 TGCCTGCCTCAGCCCCACTGCGAGACTCACACAGCCCCCCAACCCCCGAGGCCGCTGCTTATCTG TGCCTGCCTCAGCCCCACTGCGAGACTCACACGGCCCCCCAACCCCCGAGGCCGCTGCTTATCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49764055..49764138 26863196 MeRIP-seq:(Medium) rs1050631659 Functional Loss SNV dbSNP153 33..33 33 - - - 97515 RMVar_ID_97515 Human_SNP_ID_626439088 m1A Human chr17 - 49788741 49788741 49788741 GCTCCGGCGGGCTCCGTGGCGGCCTCTGTATCAGTCCCAATCCTGCGGACGATCCCTAGTGCCTC GCTCCGGCGGGCTCCGTGGCGGCCTCTGTATCGGTCCCAATCCTGCGGACGATCCCTAGTGCCTC T C FAM117A Ensembl:ENSG00000121104 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49788676..49788850 26863196 MeRIP-seq:(Medium) rs886661718 Functional Loss SNV dbSNP153 33..33 33 - - - 97516 RMVar_ID_97516 Human_SNP_ID_626491294 m1A Human chr17 - 49995128 49995128 49995128 GTGTAAGCGCCTCTCGGCCTCCCCCTCCCCCCAGACGCGGCCGGGTCCTCCCTTCGCCTTCTGGA GTGTAAGCGCCTCTCGGCCTCCCCCTCCCCCCCGACGCGGCCGGGTCCTCCCTTCGCCTTCTGGA T G DLX3 Ensembl:ENSG00000064195 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:49995083..49995209 26863196 MeRIP-seq:(Medium) rs892643725 Functional Loss SNV dbSNP153 33..33 33 - - - 97517 RMVar_ID_97517 Human_SNP_ID_626491322 m1A Human chr17 - 49995181 49995181 49995181 GTGGCTTGGGACGCGAGGAGAGGCGCGCAGCGACCGCCTGACGGCAGGCAATGGTGTAAGCGCCT GTGGCTTGGGACGCGAGGAGAGGCGCGCAGCGGCCGCCTGACGGCAGGCAATGGTGTAAGCGCCT T C DLX3 Ensembl:ENSG00000064195 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49995065..49995186 26863196 MeRIP-seq:(Medium) rs1174430335 Functional Loss SNV dbSNP153 33..33 33 - - - 97518 RMVar_ID_97518 Human_SNP_ID_626508942 m1A Human chr17 + 50056633 50056633 50056633 CTCGGTCGCCCTCCATCGGCAGACAGAGCGGCAGCAGCGCTACCTGTAAGTGAAGCTGGAGGGTG CTCGGTCGCCCTCCATCGGCAGACAGAGCGGCGGCAGCGCTACCTGTAAGTGAAGCTGGAGGGTG A G ITGA3 Ensembl:ENSG00000005884 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50056118..50063558 32194978 MeRIP-seq:(Medium) rs753121051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1836843,Human_Splice_Rec_1836867,Human_Splice_Rec_1836913,Human_Splice_Rec_1836963,Human_Splice_Rec_1837011 RMVar_hsa_circ_185186,RMVar_hsa_circ_89683 97519 RMVar_ID_97519 Human_SNP_ID_626512349 m1A Human chr17 - 50070929 50070929 50070929 CCACTTGATGGGCTACCACTACTGTACTCACCAATATAGAGGTTTCCTTGGTCCTCTGGGTCCTT CCACTTGATGGGCTACCACTACTGTACTCACCGATATAGAGGTTTCCTTGGTCCTCTGGGTCCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50070926..50070950 32194978 MeRIP-seq:(Medium) rs368380539 Functional Loss SNV dbSNP153 33..33 33 - - - 97520 RMVar_ID_97520 Human_SNP_ID_626512498 m1A Human chr17 - 50071452 50071452 50071452 TGCCAAAATAGGCGCCCACCTGCGAGCCCTCCAGCACCTGCCTCCTCCGCAGGTCTCCGCCTGCC TGCCAAAATAGGCGCCCACCTGCGAGCCCTCCCGCACCTGCCTCCTCCGCAGGTCTCCGCCTGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50071402..50071517 26863196 MeRIP-seq:(Medium) rs1205896489 Functional Loss SNV dbSNP153 33..33 33 - - - 97521 RMVar_ID_97521 Human_SNP_ID_626513098 m1A Human chr17 - 50073936 50073936 50073936 GTGATAGATGTACACTTTGCCCAAGCCTTCAAACGGAGCTCCCACAGCAATATCTGCAGAAGAAA GTGATAGATGTACACTTTGCCCAAGCCTTCAAGCGGAGCTCCCACAGCAATATCTGCAGAAGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50072102..50073935 32194978 MeRIP-seq:(Medium) rs1199203710 Functional Loss SNV dbSNP153 33..33 33 - - - 97522 RMVar_ID_97522 Human_SNP_ID_626514088 m1A Human chr17 - 50076954 50076954 50076954 GCTGTACTGGAGCCTGAGAGCAGGAGCCCAGGACTCAGCCAAGAGCCCCGCCCCCAGGGCACTCC GCTGTACTGGAGCCTGAGAGCAGGAGCCCAGGGCTCAGCCAAGAGCCCCGCCCCCAGGGCACTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50076951..50077145 32194978 MeRIP-seq:(Medium) rs947222296 Functional Loss SNV dbSNP153 33..33 33 - - - 97523 RMVar_ID_97523 Human_SNP_ID_626514784 m1A Human chr17 + 50079175 50079175 50079175 AAGTCAGCAATGGCAAGTGGCTGCTGTATCCCACGGAGATCACCGTCCATGGCAATGGGTCCTGG AAGTCAGCAATGGCAAGTGGCTGCTGTATCCCGCGGAGATCACCGTCCATGGCAATGGGTCCTGG A G ITGA3 Ensembl:ENSG00000005884 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50079125..50079226 32194978 MeRIP-seq:(Medium) rs867027896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130282 Human_Splice_Rec_1836900,Human_Splice_Rec_1836901,Human_Splice_Rec_1836950,Human_Splice_Rec_1836951,Human_Splice_Rec_1837000,Human_Splice_Rec_1837001,Human_Splice_Rec_1837060,Human_Splice_Rec_1837061 Human_miRNA_ID_2465155 RMVar_hsa_circ_185186,RMVar_hsa_circ_89683,RMVar_hsa_circ_121818,RMVar_hsa_circ_124085,RMVar_hsa_circ_185196,RMVar_hsa_circ_114628,RMVar_hsa_circ_78895,RMVar_hsa_circ_185198,RMVar_hsa_circ_185199,RMVar_hsa_circ_86401,RMVar_hsa_circ_120952,RMVar_hsa_circ_185200,RMVar_hsa_circ_185203,RMVar_hsa_circ_185204,RMVar_hsa_circ_371089,RMVar_hsa_circ_84842,RMVar_hsa_circ_94524,RMVar_hsa_circ_185213,RMVar_hsa_circ_185214,RMVar_hsa_circ_185215,RMVar_hsa_circ_80768,RMVar_hsa_circ_185216,RMVar_hsa_circ_106065,RMVar_hsa_circ_115154,RMVar_hsa_circ_185223,RMVar_hsa_circ_185222,RMVar_hsa_circ_122182,RMVar_hsa_circ_120554,RMVar_hsa_circ_185227,RMVar_hsa_circ_108684,RMVar_hsa_circ_82116,RMVar_hsa_circ_185228,RMVar_hsa_circ_185229,RMVar_hsa_circ_91822,RMVar_hsa_circ_23890,RMVar_hsa_circ_79347,RMVar_hsa_circ_185230,RMVar_hsa_circ_185231,RMVar_hsa_circ_79837,RMVar_hsa_circ_185237,RMVar_hsa_circ_43923,RMVar_hsa_circ_185236 97524 RMVar_ID_97524 Human_SNP_ID_626517729 m1A Human chr17 + 50089233 50089233 50089233 GGAGCACCCTGCCCACCAAGAAGCACTGGGTGACCAGCTGGCAGACTCGGGACCAATACTACTGA GGAGCACCCTGCCCACCAAGAAGCACTGGGTGGCCAGCTGGCAGACTCGGGACCAATACTACTGA A G ITGA3 Ensembl:ENSG00000005884 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50089184..50089249 26863196 MeRIP-seq:(Medium) rs1343930328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5577483,Human_RBP_ID_27454178 Human_miRNA_ID_272287,Human_miRNA_ID_2455803 RMVar_hsa_circ_185186,RMVar_hsa_circ_89683,RMVar_hsa_circ_121818,RMVar_hsa_circ_185196,RMVar_hsa_circ_114628,RMVar_hsa_circ_78895,RMVar_hsa_circ_185199,RMVar_hsa_circ_120952,RMVar_hsa_circ_185200,RMVar_hsa_circ_185204,RMVar_hsa_circ_84842,RMVar_hsa_circ_185215,RMVar_hsa_circ_80768,RMVar_hsa_circ_185216,RMVar_hsa_circ_108684,RMVar_hsa_circ_82116,RMVar_hsa_circ_185229,RMVar_hsa_circ_94663,RMVar_hsa_circ_79347,RMVar_hsa_circ_185230,RMVar_hsa_circ_109370,RMVar_hsa_circ_185237,RMVar_hsa_circ_185240,RMVar_hsa_circ_104957,RMVar_hsa_circ_185241,RMVar_hsa_circ_84424,RMVar_hsa_circ_185242,RMVar_hsa_circ_185243 97525 RMVar_ID_97525 Human_SNP_ID_626518032 m1A Human chr17 - 50090285 50090285 50090285 CAGCTTCTCAAATGGGCCTTAGGACACAGCCCATGGGGGAGGGGGCAGAGCCAGGCTGGCTCTGA CAGCTTCTCAAATGGGCCTTAGGACACAGCCCTTGGGGGAGGGGGCAGAGCCAGGCTGGCTCTGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50089926..50090475 32194978 MeRIP-seq:(Medium) rs756840406 Functional Loss SNV dbSNP153 33..33 33 - - - 97526 RMVar_ID_97526 Human_SNP_ID_626518033 m1A Human chr17 - 50090285 50090285 50090285 CAGCTTCTCAAATGGGCCTTAGGACACAGCCCATGGGGGAGGGGGCAGAGCCAGGCTGGCTCTGA CAGCTTCTCAAATGGGCCTTAGGACACAGCCCGTGGGGGAGGGGGCAGAGCCAGGCTGGCTCTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50089926..50090475 32194978 MeRIP-seq:(Medium) rs756840406 Functional Loss SNV dbSNP153 33..33 33 - - - 97527 RMVar_ID_97527 Human_SNP_ID_626519388 m1A Human chr17 - 50095473 50095473 50095473 TGAAGTGCTCTATGTACTTGGGCGCCCCTGCCAGGGACGCATTCTTCAGCAGCGCCCACACCCAG TGAAGTGCTCTATGTACTTGGGCGCCCCTGCCGGGGACGCATTCTTCAGCAGCGCCCACACCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:50095389..50095525;chr17:50095422..50095583 26863196 MeRIP-seq:(Medium) rs1377098582 Functional Loss SNV dbSNP153 33..33 33 - - - 97528 RMVar_ID_97528 Human_SNP_ID_626521911 m1A Human chr17 + 50105959 50105956 50105960 CGTGGTGCCCACCATGGCACAAGGCGTGCTTGAGTACAAGGACACCTACGGCGATGACCCCGTCT CGTGGTGCCCACCATGGCACAAGGCGTGCT____TACAAGGACACCTACGGCGATGACCCCGTCT TTGAG T PDK2 Ensembl:ENSG00000005882 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50105887..50106037 32194978 MeRIP-seq:(Medium) rs761344147 Functional Loss DEL dbSNP153 31..34 33 - - - Human_Splice_Rec_1837080,Human_Splice_Rec_1837100,Human_Splice_Rec_1837108,Human_Splice_Rec_1837124,Human_Splice_Rec_1837146,Human_Splice_Rec_1837152,Human_Splice_Rec_1837162,Human_Splice_Rec_1837186,Human_Splice_Rec_1837190,Human_Splice_Rec_1837198,Human_Splice_Rec_1837208 RMVar_hsa_circ_27540,RMVar_hsa_circ_75109 97529 RMVar_ID_97529 Human_SNP_ID_626524626 m1A Human chr17 - 50115649 50115649 50115649 CCTGCCTTTTTCCTGGTTCACGGACAGCGGCAAGGGCTCAGCATCCTCGGGTAGCACCACCTCCC CCTGCCTTTTTCCTGGTTCACGGACAGCGGCAGGGGCTCAGCATCCTCGGGTAGCACCACCTCCC T C SAMD14 Ensembl:ENSG00000167100 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50115603..50116007 32194978 MeRIP-seq:(Medium) rs1274039265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837244,Human_Splice_Rec_1837245,Human_Splice_Rec_1837260,Human_Splice_Rec_1837261,Human_Splice_Rec_1837272,Human_Splice_Rec_1837273,Human_Splice_Rec_1837290,Human_Splice_Rec_1837291,Human_Splice_Rec_1837302,Human_Splice_Rec_1837303 97530 RMVar_ID_97530 Human_SNP_ID_626529604 m1A Human chr17 + 50134026 50134026 50134026 AGGGGTGGGGACAAGAAATACTGATCGAAGTCATGGTCTATTTACAGGGGACAAGAAGCCAAAAC AGGGGTGGGGACAAGAAATACTGATCGAAGTCGTGGTCTATTTACAGGGGACAAGAAGCCAAAAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50133909..50134050 26863196 MeRIP-seq:(Medium) rs989408456 Functional Loss SNV dbSNP153 33..33 33 - - - 97531 RMVar_ID_97531 Human_SNP_ID_626529839 m1A Human chr17 + 50134877 50134867 50134877 CGGCACAATGATGGGGGGAGAGGGAAGGGCCGAGAAGGTAGAATCTCAAGTCAAGAGGCCCAGGG CGGCACAATGATGGGGGGAGAGG__________GAAGGTAGAATCTCAAGTCAAGAGGCCCAGGG GGAAGGGCCGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50134569..50135138 26863196 MeRIP-seq:(Medium) rs1368691189 Functional Loss DEL dbSNP153 24..33 33 - - - 97532 RMVar_ID_97532 Human_SNP_ID_626529936 m1A Human chr17 - 50135262 50135262 50135262 CCTCCCATTGTCCTCCCTCCCCTGTCCTCAACACCCCACCCCTCCCCCTTCCAGCCTGGGGACAG CCTCCCATTGTCCTCCCTCCCCTGTCCTCAACGCCCCACCCCTCCCCCTTCCAGCCTGGGGACAG T C PPP1R9B Ensembl:ENSG00000108819 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50135212..50135330 26863196 MeRIP-seq:(Medium) rs1276305617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3543041,Human_RBP_ID_5143288,Human_RBP_ID_17080742,Human_RBP_ID_18941851,Human_RBP_ID_27454220 Human_miRNA_ID_464912,Human_miRNA_ID_1321697,Human_miRNA_ID_1560164,Human_miRNA_ID_2153768,Human_miRNA_ID_2385700,Human_miRNA_ID_2801645,Human_miRNA_ID_3009776 97533 RMVar_ID_97533 Human_SNP_ID_626530077 m1A Human chr17 - 50135617 50135617 50135617 GGAGATCGAGTTCCTGAAAAAGGAGACTGCACAGCGTCGGGTTCTGGAGGAGTCGGAGCTGGCCA GGAGATCGAGTTCCTGAAAAAGGAGACTGCACGGCGTCGGGTTCTGGAGGAGTCGGAGCTGGCCA T C PPP1R9B Ensembl:ENSG00000108819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50135566..50135654 26863196 MeRIP-seq:(Medium) rs1298477661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493181,Human_RBP_ID_4437162 Human_Splice_Rec_1837336,Human_Splice_Rec_1837337 RMVar_hsa_circ_105545,RMVar_hsa_circ_185246 97534 RMVar_ID_97534 Human_SNP_ID_626531214 m1A Human chr17 - 50140130 50140130 50140130 GGAACAGGAGCGATGGCAGCGGGAGATGATGGAGCAGAGATACGCCCAGTATGGGGAGGATGACG GGAACAGGAGCGATGGCAGCGGGAGATGATGGGGCAGAGATACGCCCAGTATGGGGAGGATGACG T C PPP1R9B Ensembl:ENSG00000108819 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50135585..50140157 32194978 MeRIP-seq:(Medium) rs781550890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952664,Human_RBP_ID_9290207,Human_RBP_ID_9376329,Human_RBP_ID_13064480,Human_RBP_ID_23733881,Human_RBP_ID_26332041 Human_Splice_Rec_1837328,Human_Splice_Rec_1837329,Human_Splice_Rec_1837345 Human_miRNA_ID_2924403 RMVar_hsa_circ_185248,RMVar_hsa_circ_122262,RMVar_hsa_circ_332463,RMVar_hsa_circ_185247 97535 RMVar_ID_97535 Human_SNP_ID_626531215 m1A Human chr17 - 50140130 50140130 50140130 GGAACAGGAGCGATGGCAGCGGGAGATGATGGAGCAGAGATACGCCCAGTATGGGGAGGATGACG GGAACAGGAGCGATGGCAGCGGGAGATGATGGCGCAGAGATACGCCCAGTATGGGGAGGATGACG T G PPP1R9B Ensembl:ENSG00000108819 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50135585..50140157 32194978 MeRIP-seq:(Medium) rs781550890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952664,Human_RBP_ID_9290207,Human_RBP_ID_9376329,Human_RBP_ID_13064480,Human_RBP_ID_23733881,Human_RBP_ID_26332041 Human_Splice_Rec_1837328,Human_Splice_Rec_1837329,Human_Splice_Rec_1837345 Human_miRNA_ID_2924403 RMVar_hsa_circ_185248,RMVar_hsa_circ_122262,RMVar_hsa_circ_332463,RMVar_hsa_circ_185247 97536 RMVar_ID_97536 Human_SNP_ID_626533634 m1A Human chr17 - 50149377 50149377 50149377 GGCCGGGCCCCGGACGTGGCCCCTGAGGAGGTAGATGAATCCAAGAAGGAGGACTTCTCGGAGGC GGCCGGGCCCCGGACGTGGCCCCTGAGGAGGTGGATGAATCCAAGAAGGAGGACTTCTCGGAGGC T C PPP1R9B Ensembl:ENSG00000108819 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50149251..50149800 26863196 MeRIP-seq:(Medium) rs199865066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1862122,Human_RBP_ID_4437212,Human_RBP_ID_8824834,Human_RBP_ID_13064497,Human_RBP_ID_22715784,Human_RBP_ID_27561171,Human_RBP_ID_27814030 Clinvar_Rec_590 97537 RMVar_ID_97537 Human_SNP_ID_626533645 m1A Human chr17 + 50149393 50149393 50149393 CCTTCTTGGATTCATCTACCTCCTCAGGGGCCACGTCCGGGGCCCGGCCATTGCCCACCCCCCTC CCTTCTTGGATTCATCTACCTCCTCAGGGGCCGCGTCCGGGGCCCGGCCATTGCCCACCCCCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50141221..50149825 26863196 MeRIP-seq:(Medium) rs762411750 Functional Loss SNV dbSNP153 33..33 33 - - - 97538 RMVar_ID_97538 Human_SNP_ID_626534260 m1A Human chr17 + 50150774 50150774 50150774 AAGCTGCCGAAGACAGCCAGCCCCGCTTCAAAAGCCCGAGCGGCCTGGTACGGTCGCCCCCACCC AAGCTGCCGAAGACAGCCAGCCCCGCTTCAAAGGCCCGAGCGGCCTGGTACGGTCGCCCCCACCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50150726..50151025 26863196 MeRIP-seq:(Medium) rs575754859 Functional Loss SNV dbSNP153 33..33 33 - - - 97539 RMVar_ID_97539 Human_SNP_ID_626543342 m1A Human chr17 - 50184300 50184300 50184300 TCCTCTGAAACCCTCCTCCACAGCTGCAGCCCATCCTCCCGGCTCCCTCCTAGTCTGTCCTGCGT TCCTCTGAAACCCTCCTCCACAGCTGCAGCCCTTCCTCCCGGCTCCCTCCTAGTCTGTCCTGCGT T A COL1A1 Ensembl:ENSG00000108821 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50184249..50184361 26863196 MeRIP-seq:(Medium) rs370496085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_86365,Human_miRNA_ID_2467390 RMVar_hsa_circ_83975,RMVar_hsa_circ_99122,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185259,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250 97540 RMVar_ID_97540 Human_SNP_ID_626543763 m1A Human chr17 - 50185466 50185466 50185466 CCCTCCATCCCAACCTGGCTCCCTCCCACCCAACCAACTTTCCCCCCAACCCGGAAACAGACAAG CCCTCCATCCCAACCTGGCTCCCTCCCACCCACCCAACTTTCCCCCCAACCCGGAAACAGACAAG T G COL1A1 Ensembl:ENSG00000108821 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr17:50185401..50185575;chr17:50185339..50185558 26863196 MeRIP-seq:(Medium) rs895430341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130760,Human_RBP_ID_23733919,Human_RBP_ID_27454246 Human_miRNA_ID_2946233 RMVar_hsa_circ_83975,RMVar_hsa_circ_99122,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185259,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250 97541 RMVar_ID_97541 Human_SNP_ID_626544310 m1A Human chr17 - 50186777 50186777 50186777 CTACCGGGCTGATGATGCCAATGTGGTTCGTGACCGTGACCTCGAGGTGGACACCACCCTCAAGA CTACCGGGCTGATGATGCCAATGTGGTTCGTGGCCGTGACCTCGAGGTGGACACCACCCTCAAGA T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50186726..50186800 26863196 MeRIP-seq:(Medium) rs1319157667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5577489 Human_miRNA_ID_2515247 RMVar_hsa_circ_20329,RMVar_hsa_circ_83975,RMVar_hsa_circ_99122,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185259,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_100730,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185266,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260 97542 RMVar_ID_97542 Human_SNP_ID_626544331 m1A Human chr17 - 50186807 50186807 50186807 TCAAGAGAAGGCTCACGATGGTGGCCGCTACTACCGGGCTGATGATGCCAATGTGGTTCGTGACC TCAAGAGAAGGCTCACGATGGTGGCCGCTACTGCCGGGCTGATGATGCCAATGTGGTTCGTGACC T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50186626..50187668 26863196 MeRIP-seq:(Medium) rs1555571849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493199,Human_RBP_ID_8456257 Human_miRNA_ID_2577565 Clinvar_Rec_591 RMVar_hsa_circ_20329,RMVar_hsa_circ_83975,RMVar_hsa_circ_99122,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185259,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_100730,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185266,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260 97543 RMVar_ID_97543 Human_SNP_ID_626544390 m1A Human chr17 - 50186924 50186922 50186925 CCGGTAATCCCCACTCTCTTCCCTCTCTGTGCAGGGTCCCCCCGGCCCTCCTGGACCTCCTGGTC CCGGTAATCCCCACTCTCTTCCCTCTCTGTG___GGTCCCCCCGGCCCTCCTGGACCTCCTGGTC CCTG C COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50186911..50187011 26863196 MeRIP-seq:(Medium) rs72656328 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8456258 RMVar_hsa_circ_20329,RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_100730,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185266,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260 97544 RMVar_ID_97544 Human_SNP_ID_626544495 m1A Human chr17 + 50187120 50187120 50187120 TCTTTGCCAGGAGCACCAGCAGAGCCAGGGGGACCCTGGAGTGGGGGAAATGGTTTGAGAAAGGC TCTTTGCCAGGAGCACCAGCAGAGCCAGGGGGCCCCTGGAGTGGGGGAAATGGTTTGAGAAAGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50186308..50187618 32194978 MeRIP-seq:(Medium) rs765800843 Functional Loss SNV dbSNP153 33..33 33 - - - 97545 RMVar_ID_97545 Human_SNP_ID_626544759 m1A Human chr17 + 50187966 50187966 50187966 TCGCCCTGTTCGCCTGTCTCACCCTTGTCACCACGGGGGCCTTGGGGTCCCTAGAAGAGAGAAAG TCGCCCTGTTCGCCTGTCTCACCCTTGTCACCCCGGGGGCCTTGGGGTCCCTAGAAGAGAGAAAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50187876..50187975 26863196 MeRIP-seq:(Medium) rs1219747923 Functional Loss SNV dbSNP153 33..33 33 - - - 97546 RMVar_ID_97546 Human_SNP_ID_626544803 m1A Human chr17 + 50188078 50188078 50188078 TCTGCATCTGTAGAGTTCTAAAGGCATGGGGGACACAGCAGGGTACTTACGGCGGGGCCACGGGC TCTGCATCTGTAGAGTTCTAAAGGCATGGGGGGCACAGCAGGGTACTTACGGCGGGGCCACGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50188076..50188150 26863196 MeRIP-seq:(Medium) rs759589224 Functional Loss SNV dbSNP153 33..33 33 - - - 97547 RMVar_ID_97547 Human_SNP_ID_626545357 m1A Human chr17 - 50189444 50189444 50189444 TGGTGAGACTGGCCCTGCTGGACGTCCTGGTGAAGTTGGTCCCCCTGGTCCCCCTGGCCCTGCTG TGGTGAGACTGGCCCTGCTGGACGTCCTGGTGTAGTTGGTCCCCCTGGTCCCCCTGGCCCTGCTG T A COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50188505..50190485 26863196 MeRIP-seq:(Medium) rs774442705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837528,Human_Splice_Rec_1837529 Human_miRNA_ID_1336564,Human_miRNA_ID_1353488 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_269130,RMVar_hsa_circ_185260,RMVar_hsa_circ_267259,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_266404,RMVar_hsa_circ_90849,RMVar_hsa_circ_83018,RMVar_hsa_circ_112441,RMVar_hsa_circ_185272,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_185277,RMVar_hsa_circ_350123,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_94482,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268118,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_67966,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_185284 97548 RMVar_ID_97548 Human_SNP_ID_626545358 m1A Human chr17 - 50189444 50189444 50189444 TGGTGAGACTGGCCCTGCTGGACGTCCTGGTGAAGTTGGTCCCCCTGGTCCCCCTGGCCCTGCTG TGGTGAGACTGGCCCTGCTGGACGTCCTGGTGGAGTTGGTCCCCCTGGTCCCCCTGGCCCTGCTG T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50188505..50190485 26863196 MeRIP-seq:(Medium) rs774442705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837528,Human_Splice_Rec_1837529 Human_miRNA_ID_1336564,Human_miRNA_ID_1353488 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_269130,RMVar_hsa_circ_185260,RMVar_hsa_circ_267259,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_266404,RMVar_hsa_circ_90849,RMVar_hsa_circ_83018,RMVar_hsa_circ_112441,RMVar_hsa_circ_185272,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_185277,RMVar_hsa_circ_350123,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_94482,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268118,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_67966,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_185284 97549 RMVar_ID_97549 Human_SNP_ID_626545635 m1A Human chr17 - 50190083 50190083 50190083 CCCCCAGGGTGCTGACGGCCAACCTGGTGCTAAAGGCGAACCTGGTGATGCTGGTGCTAAAGGCG CCCCCAGGGTGCTGACGGCCAACCTGGTGCTAGAGGCGAACCTGGTGATGCTGGTGCTAAAGGCG T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50188564..50190435 32194978 MeRIP-seq:(Medium) rs1351147197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837522,Human_Splice_Rec_1837523 Human_miRNA_ID_739488,Human_miRNA_ID_743503,Human_miRNA_ID_747508 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_269130,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_266404,RMVar_hsa_circ_90849,RMVar_hsa_circ_83018,RMVar_hsa_circ_112441,RMVar_hsa_circ_185272,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_185277,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_94482,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268118,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_118138,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_185284,RMVar_hsa_circ_185288,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_370139,RMVar_hsa_circ_117878,RMVar_hsa_circ_125541,RMVar_hsa_circ_185289,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_101218,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185291,RMVar_hsa_circ_185292 97550 RMVar_ID_97550 Human_SNP_ID_626545650 m1A Human chr17 - 50190110 50190110 50190110 TTCCCTCCATTCACCGCCCTGCTTCCTCCCCCAGGGTGCTGACGGCCAACCTGGTGCTAAAGGCG TTCCCTCCATTCACCGCCCTGCTTCCTCCCCCGGGGTGCTGACGGCCAACCTGGTGCTAAAGGCG T C COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50190076..50190125 26863196 MeRIP-seq:(Medium) rs72651666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_98517,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_269130,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_266404,RMVar_hsa_circ_90849,RMVar_hsa_circ_83018,RMVar_hsa_circ_112441,RMVar_hsa_circ_185272,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_185277,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_94482,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_118138,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_185284,RMVar_hsa_circ_185288,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_117878,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_101218,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185291,RMVar_hsa_circ_185292 97551 RMVar_ID_97551 Human_SNP_ID_626545921 m1A Human chr17 + 50190854 50190854 50190854 CACCAGGGGCACCAGCAGGGCCAGGAGGACCAATGGGGCCAGTCAGACCACGGACGCCATCTTTG CACCAGGGGCACCAGCAGGGCCAGGAGGACCAGTGGGGCCAGTCAGACCACGGACGCCATCTTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50190584..50192052 32194978 MeRIP-seq:(Medium) rs1339732084 Functional Loss SNV dbSNP153 33..33 33 - - - 97552 RMVar_ID_97552 Human_SNP_ID_626546112 m1A Human chr17 - 50191456 50191456 50191456 TGATGCTGGTGCCCCTGGAGCTCCCGGTAGCCAGGGCGCCCCTGGCCTTCAGGGAATGCCTGGTG TGATGCTGGTGCCCCTGGAGCTCCCGGTAGCCGGGGCGCCCCTGGCCTTCAGGGAATGCCTGGTG T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50191387..50191500 26863196 MeRIP-seq:(Medium) rs1419591590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837514,Human_Splice_Rec_1837515,Human_Splice_Rec_1837574,Human_Splice_Rec_1837575 Human_miRNA_ID_2452794 RMVar_hsa_circ_5780,RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_100414,RMVar_hsa_circ_98517,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_118688,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185265,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_266404,RMVar_hsa_circ_83018,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_185277,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_94482,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_118138,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_185284,RMVar_hsa_circ_185288,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_117878,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_101218,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185291,RMVar_hsa_circ_185292,RMVar_hsa_circ_185297,RMVar_hsa_circ_126004,RMVar_hsa_circ_351289 97553 RMVar_ID_97553 Human_SNP_ID_626546690 m1A Human chr17 - 50192852 50192852 50192852 TAACCCTGAGTTCCCCTTTGCTCTCTCCCTGCAGGGTCCTGCTGGCAAAGATGGAGAGGCTGGAG TAACCCTGAGTTCCCCTTTGCTCTCTCCCTGCCGGGTCCTGCTGGCAAAGATGGAGAGGCTGGAG T G COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr17:50192776..50192875;chr17:50192484..50193529 26863196,32194978 MeRIP-seq:(Medium) rs72651617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837505,Human_Splice_Rec_1837565 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_185251,RMVar_hsa_circ_77039,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_102821,RMVar_hsa_circ_117610,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185264,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_117878,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185292,RMVar_hsa_circ_185297,RMVar_hsa_circ_126004,RMVar_hsa_circ_24172,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299 97554 RMVar_ID_97554 Human_SNP_ID_626547095 m1A Human chr17 + 50194021 50194021 50194021 CGGGCACCAGGTGGGCCTGGGGGTCCGGGGCGACCATCTTGACCGGCGGGACCCTAAGGATGGGA CGGGCACCAGGTGGGCCTGGGGGTCCGGGGCGGCCATCTTGACCGGCGGGACCCTAAGGATGGGA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:50193926..50194100 26863196 MeRIP-seq:(Medium) rs1555573640 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_592 97555 RMVar_ID_97555 Human_SNP_ID_626547097 m1A Human chr17 - 50194027 50194027 50194027 CGTGCCTCCCATCCTTAGGGTCCCGCCGGTCAAGATGGTCGCCCCGGACCCCCAGGCCCACCTGG CGTGCCTCCCATCCTTAGGGTCCCGCCGGTCAGGATGGTCGCCCCGGACCCCCAGGCCCACCTGG T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50193869..50194175 26863196 MeRIP-seq:(Medium) rs751582370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837500,Human_Splice_Rec_1837501,Human_Splice_Rec_1837561,Human_Splice_Rec_1837582 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_185251,RMVar_hsa_circ_77039,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_117610,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185297,RMVar_hsa_circ_126004,RMVar_hsa_circ_24172,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_88128,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_376861,RMVar_hsa_circ_118132,RMVar_hsa_circ_185301,RMVar_hsa_circ_185302 97556 RMVar_ID_97556 Human_SNP_ID_626547098 m1A Human chr17 - 50194027 50194027 50194027 CGTGCCTCCCATCCTTAGGGTCCCGCCGGTCAAGATGGTCGCCCCGGACCCCCAGGCCCACCTGG CGTGCCTCCCATCCTTAGGGTCCCGCCGGTCACGATGGTCGCCCCGGACCCCCAGGCCCACCTGG T G COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50193869..50194175 26863196 MeRIP-seq:(Medium) rs751582370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837500,Human_Splice_Rec_1837501,Human_Splice_Rec_1837561,Human_Splice_Rec_1837582 RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_185251,RMVar_hsa_circ_77039,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_117610,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185263,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_100034,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185283,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_92669,RMVar_hsa_circ_185285,RMVar_hsa_circ_185286,RMVar_hsa_circ_95435,RMVar_hsa_circ_185287,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185297,RMVar_hsa_circ_126004,RMVar_hsa_circ_24172,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_88128,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_376861,RMVar_hsa_circ_118132,RMVar_hsa_circ_185301,RMVar_hsa_circ_185302 97557 RMVar_ID_97557 Human_SNP_ID_626547110 m1A Human chr17 - 50194043 50194043 50194043 TCCTCACTGCTGCTTTCGTGCCTCCCATCCTTAGGGTCCCGCCGGTCAAGATGGTCGCCCCGGAC TCCTCACTGCTGCTTTCGTGCCTCCCATCCTTGGGGTCCCGCCGGTCAAGATGGTCGCCCCGGAC T C COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:50194005..50194139;chr17:50194013..50194125 26863196 MeRIP-seq:(Medium) rs72648362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_185251,RMVar_hsa_circ_77039,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_86689,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185268,RMVar_hsa_circ_185269,RMVar_hsa_circ_111296,RMVar_hsa_circ_185270,RMVar_hsa_circ_185271,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_88934,RMVar_hsa_circ_112302,RMVar_hsa_circ_185280,RMVar_hsa_circ_185282,RMVar_hsa_circ_79365,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_185286,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185293,RMVar_hsa_circ_93507,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_185297,RMVar_hsa_circ_126004,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_88128,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_376861,RMVar_hsa_circ_118132,RMVar_hsa_circ_185301,RMVar_hsa_circ_185302 97558 RMVar_ID_97558 Human_SNP_ID_626547492 m1A Human chr17 - 50194830 50194830 50194830 CCACAGGCCGCCTCCTCCTCTCGGCCCTCTCCAGGGCCCTGTTGGTGTTCAAGGACCCCCTGGCC CCACAGGCCGCCTCCTCCTCTCGGCCCTCTCCGGGGCCCTGTTGGTGTTCAAGGACCCCCTGGCC T C COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50193901..50194850 26863196 MeRIP-seq:(Medium) rs72648338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83975,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_185251,RMVar_hsa_circ_77039,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250,RMVar_hsa_circ_86750,RMVar_hsa_circ_80079,RMVar_hsa_circ_77454,RMVar_hsa_circ_101681,RMVar_hsa_circ_80462,RMVar_hsa_circ_82256,RMVar_hsa_circ_185261,RMVar_hsa_circ_185262,RMVar_hsa_circ_185260,RMVar_hsa_circ_101128,RMVar_hsa_circ_265096,RMVar_hsa_circ_185267,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_112441,RMVar_hsa_circ_185273,RMVar_hsa_circ_122415,RMVar_hsa_circ_185275,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_185274,RMVar_hsa_circ_98323,RMVar_hsa_circ_114932,RMVar_hsa_circ_112302,RMVar_hsa_circ_185280,RMVar_hsa_circ_79365,RMVar_hsa_circ_185281,RMVar_hsa_circ_185278,RMVar_hsa_circ_185279,RMVar_hsa_circ_268590,RMVar_hsa_circ_122468,RMVar_hsa_circ_185286,RMVar_hsa_circ_125541,RMVar_hsa_circ_185290,RMVar_hsa_circ_123206,RMVar_hsa_circ_185295,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_185294,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_88128,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_118132,RMVar_hsa_circ_123517,RMVar_hsa_circ_185301,RMVar_hsa_circ_185302,RMVar_hsa_circ_87905,RMVar_hsa_circ_116255,RMVar_hsa_circ_185304,RMVar_hsa_circ_185305,RMVar_hsa_circ_80272,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_185308,RMVar_hsa_circ_353007 97559 RMVar_ID_97559 Human_SNP_ID_626547771 m1A Human chr17 + 50195449 50195449 50195449 CCTGGCAGGATACTTACATTGGCACCTTTAGCACCAGGCTGTCCATCAGCACCAGGGTTTCCCTG CCTGGCAGGATACTTACATTGGCACCTTTAGCGCCAGGCTGTCCATCAGCACCAGGGTTTCCCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50195426..50195500 26863196 MeRIP-seq:(Medium) rs757681709 Functional Loss SNV dbSNP153 33..33 33 - - - 97560 RMVar_ID_97560 Human_SNP_ID_626548935 m1A Human chr17 - 50198506 50198506 50198506 CTGTCCTCACTCTGACTTCTCTTGTTTGTTCTAGAACTTTGCTCCCCAGCTGTCTTATGGCTATG CTGTCCTCACTCTGACTTCTCTTGTTTGTTCTTGAACTTTGCTCCCCAGCTGTCTTATGGCTATG T A COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50198151..50198553 26863196 MeRIP-seq:(Medium) rs72667019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837463,Human_Splice_Rec_1837599 Clinvar_Rec_593 RMVar_hsa_circ_86750,RMVar_hsa_circ_101128,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_112302,RMVar_hsa_circ_185278,RMVar_hsa_circ_185290,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_84453,RMVar_hsa_circ_185310,RMVar_hsa_circ_97631,RMVar_hsa_circ_185315 97561 RMVar_ID_97561 Human_SNP_ID_626548936 m1A Human chr17 - 50198506 50198506 50198506 CTGTCCTCACTCTGACTTCTCTTGTTTGTTCTAGAACTTTGCTCCCCAGCTGTCTTATGGCTATG CTGTCCTCACTCTGACTTCTCTTGTTTGTTCTGGAACTTTGCTCCCCAGCTGTCTTATGGCTATG T C COL1A1 Ensembl:ENSG00000108821 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50198151..50198553 26863196 MeRIP-seq:(Medium) rs72667019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837463,Human_Splice_Rec_1837599 Clinvar_Rec_593 RMVar_hsa_circ_86750,RMVar_hsa_circ_101128,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_112302,RMVar_hsa_circ_185278,RMVar_hsa_circ_185290,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_84453,RMVar_hsa_circ_185310,RMVar_hsa_circ_97631,RMVar_hsa_circ_185315 97562 RMVar_ID_97562 Human_SNP_ID_626549155 m1A Human chr17 - 50199302 50199302 50199302 CCTGCAGGGACCCGCAGGCCCCCCTGGCCGAGATGGCATCCCTGGACAGCCTGGACTTCCCGGAC CCTGCAGGGACCCGCAGGCCCCCCTGGCCGAGGTGGCATCCCTGGACAGCCTGGACTTCCCGGAC T C COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50199251..50199350 26863196 MeRIP-seq:(Medium) rs746847841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837460,Human_Splice_Rec_1837461,Human_Splice_Rec_1837618,Human_Splice_Rec_1837624 RMVar_hsa_circ_86750,RMVar_hsa_circ_101128,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_112302,RMVar_hsa_circ_185278,RMVar_hsa_circ_185290,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_84453,RMVar_hsa_circ_185310,RMVar_hsa_circ_97631,RMVar_hsa_circ_185315 97563 RMVar_ID_97563 Human_SNP_ID_626549240 m1A Human chr17 - 50199451 50199451 50199451 CCTCTTGTTTCTTCTCCCCCAATCCCACAGGGACCCAAGGGAGACACTGGCCCCCGAGGCCCAAG CCTCTTGTTTCTTCTCCCCCAATCCCACAGGGTCCCAAGGGAGACACTGGCCCCCGAGGCCCAAG T A COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50198690..50200250 26863196 MeRIP-seq:(Medium) rs749946056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837458,Human_Splice_Rec_1837459,Human_Splice_Rec_1837617,Human_Splice_Rec_1837622,Human_Splice_Rec_1837623 RMVar_hsa_circ_101128,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_97631,RMVar_hsa_circ_185315,RMVar_hsa_circ_13683 97564 RMVar_ID_97564 Human_SNP_ID_626549432 m1A Human chr17 - 50199797 50199797 50199797 CTGTGACGAGACCAAGAACTGCCCCGGCGCCGAAGTCCCCGAGGGCGAGTGCTGTCCCGTCTGCC CTGTGACGAGACCAAGAACTGCCCCGGCGCCGTAGTCCCCGAGGGCGAGTGCTGTCCCGTCTGCC T A COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50198690..50200014 32194978 MeRIP-seq:(Medium) rs766870668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493203 Human_Splice_Rec_1837455,Human_Splice_Rec_1837615,Human_Splice_Rec_1837619 RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_35593,RMVar_hsa_circ_107877,RMVar_hsa_circ_121780,RMVar_hsa_circ_185316,RMVar_hsa_circ_185317 97565 RMVar_ID_97565 Human_SNP_ID_626585700 m1A Human chr17 - 50346169 50346169 50346169 CCGTGGCAATCGCCAGCTTGTAGCGCCGCACCAGCTTCTGCACTCGCGCGCTCGCCACCATCTTC CCGTGGCAATCGCCAGCTTGTAGCGCCGCACCTGCTTCTGCACTCGCGCGCTCGCCACCATCTTC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:50346125..50346668 26863196 MeRIP-seq:(Medium) rs1336159526 Functional Loss SNV dbSNP153 33..33 33 - - - 97566 RMVar_ID_97566 Human_SNP_ID_626585702 m1A Human chr17 - 50346172 50346172 50346172 GCGCCGTGGCAATCGCCAGCTTGTAGCGCCGCACCAGCTTCTGCACTCGCGCGCTCGCCACCATC GCGCCGTGGCAATCGCCAGCTTGTAGCGCCGCCCCAGCTTCTGCACTCGCGCGCTCGCCACCATC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:50346126..50346715;chr17:50346123..50353894 26863196 MeRIP-seq:(Medium) rs1269448385 Functional Loss SNV dbSNP153 33..33 33 - - - 97567 RMVar_ID_97567 Human_SNP_ID_626585733 m1A Human chr17 - 50346243 50346243 50346243 CTCGCCCGCCTCGTCCTCCTCCAGGCCGCTGAAGCTCCACACTACCAGGCCCTGCAGCAGCAGGA CTCGCCCGCCTCGTCCTCCTCCAGGCCGCTGATGCTCCACACTACCAGGCCCTGCAGCAGCAGGA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50346114..50346456 26863196 MeRIP-seq:(Medium) rs1174215127 Functional Loss SNV dbSNP153 33..33 33 - - - 97568 RMVar_ID_97568 Human_SNP_ID_626585736 m1A Human chr17 - 50346253 50346253 50346253 GTCGGAGCACCTCGCCCGCCTCGTCCTCCTCCAGGCCGCTGAAGCTCCACACTACCAGGCCCTGC GTCGGAGCACCTCGCCCGCCTCGTCCTCCTCCGGGCCGCTGAAGCTCCACACTACCAGGCCCTGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50346200..50346449 26863196 MeRIP-seq:(Medium) rs1434047269 Functional Loss SNV dbSNP153 33..33 33 - - - 97569 RMVar_ID_97569 Human_SNP_ID_626587963 m1A Human chr17 + 50354552 50354552 50354552 GCTGAAGCGTCTCCTCAAGGCCGTTTATCACGAGCAGCACTTCTTTTACATCCATGTGGACAAGG GCTGAAGCGTCTCCTCAAGGCCGTTTATCACGCGCAGCACTTCTTTTACATCCATGTGGACAAGG A C XYLT2 Ensembl:ENSG00000015532 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50354501..50354600 32194978 MeRIP-seq:(Medium) rs770897347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1837789,Human_Splice_Rec_1837811,Human_Splice_Rec_1837829 Human_miRNA_ID_770339,Human_miRNA_ID_775214,Human_miRNA_ID_780053,Human_miRNA_ID_784921,Human_miRNA_ID_789747,Human_miRNA_ID_1106238,Human_miRNA_ID_1111065,Human_miRNA_ID_1599421,Human_miRNA_ID_1608874,Human_miRNA_ID_1613789,Human_miRNA_ID_1621272,Human_miRNA_ID_1637388,Human_miRNA_ID_2316795,Human_miRNA_ID_2319948,Human_miRNA_ID_2323107,Human_miRNA_ID_2326281,Human_miRNA_ID_2329375,Human_miRNA_ID_2520658,Human_miRNA_ID_2523824,Human_miRNA_ID_2775635,Human_miRNA_ID_2823009,Human_miRNA_ID_2829143,Human_miRNA_ID_2832298,Human_miRNA_ID_2836421,Human_miRNA_ID_2841773 RMVar_hsa_circ_48919,RMVar_hsa_circ_106671,RMVar_hsa_circ_348299,RMVar_hsa_circ_185319,RMVar_hsa_circ_50263,RMVar_hsa_circ_58177,RMVar_hsa_circ_71606,RMVar_hsa_circ_374705,RMVar_hsa_circ_185320 97570 RMVar_ID_97570 Human_SNP_ID_626588124 m1A Human chr17 + 50354994 50354994 50354994 AGGATGTACCTGCGGAGCATGCGGGACCTGCTAGAGGTGCCTGGCTGGGCCTGGGACTTCTTCAT AGGATGTACCTGCGGAGCATGCGGGACCTGCTGGAGGTGCCTGGCTGGGCCTGGGACTTCTTCAT A G XYLT2 Ensembl:ENSG00000015532 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50346176..50355075 32194978 MeRIP-seq:(Medium) rs1476342883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6610929,Human_RBP_ID_22953754,Human_RBP_ID_23734014 Human_Splice_Rec_1837791,Human_Splice_Rec_1837813,Human_Splice_Rec_1837831 Human_miRNA_ID_1968843 RMVar_hsa_circ_48919,RMVar_hsa_circ_106671,RMVar_hsa_circ_348299,RMVar_hsa_circ_185319,RMVar_hsa_circ_50263,RMVar_hsa_circ_58177,RMVar_hsa_circ_71606 97571 RMVar_ID_97571 Human_SNP_ID_626589276 m1A Human chr17 - 50358457 50358457 50358457 GGGTCTCACCCAGCGGTTCCCAGAACTGAAGGAGTCGAACAGTCCAGGGCCCTGGCCGCAGGGGC GGGTCTCACCCAGCGGTTCCCAGAACTGAAGGGGTCGAACAGTCCAGGGCCCTGGCCGCAGGGGC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:50358361..50358545 26863196 MeRIP-seq:(Medium) rs1423040693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13065176,Human_RBP_ID_18439261 97572 RMVar_ID_97572 Human_SNP_ID_626589764 m1A Human chr17 - 50360356 50360356 50360356 CCTGGGCCTCTGGTTCTTGCCTGTGGGAGGGGACACCCCTCCACTGTCTGTAAGGTGCAATTTCC CCTGGGCCTCTGGTTCTTGCCTGTGGGAGGGGTCACCCCTCCACTGTCTGTAAGGTGCAATTTCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50360001..50360465 32194978 MeRIP-seq:(Medium) rs1467219940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6610973 97573 RMVar_ID_97573 Human_SNP_ID_626590000 m1A Human chr17 + 50360972 50360972 50360972 TCCAGCATACCCTGCCCCTGGATGGGAAAGGCAGGGTCAGGGCCCACTGAGACCCATGCAGAGTT TCCAGCATACCCTGCCCCTGGATGGGAAAGGCTGGGTCAGGGCCCACTGAGACCCATGCAGAGTT A T XYLT2 Ensembl:ENSG00000015532 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50360763..50361062 32194978 MeRIP-seq:(Medium) rs1313556709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493240,Human_RBP_ID_5525690,Human_RBP_ID_6611002,Human_RBP_ID_18701912 Human_miRNA_ID_76269,Human_miRNA_ID_79440 RMVar_hsa_circ_106671,RMVar_hsa_circ_185319,RMVar_hsa_circ_123858,RMVar_hsa_circ_185321 97574 RMVar_ID_97574 Human_SNP_ID_626591790 m1A Human chr17 - 50367927 50367927 50367927 TCTGAAGTGACTGCTGGGAAACCCTTTGGGAGACCTGACCTGGGGCCAAAAATAAAGTGAGCCAG TCTGAAGTGACTGCTGGGAAACCCTTTGGGAGGCCTGACCTGGGGCCAAAAATAAAGTGAGCCAG T C MRPL27 Ensembl:ENSG00000108826 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50367876..50368113 26863196 MeRIP-seq:(Medium) rs1408365952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493247,Human_RBP_ID_1182828,Human_RBP_ID_1536785,Human_RBP_ID_1862158,Human_RBP_ID_3527767,Human_RBP_ID_9073314,Human_RBP_ID_13065486,Human_RBP_ID_17895604,Human_RBP_ID_26965740,Human_RBP_ID_27256570 Human_miRNA_ID_2087108 RMVar_hsa_circ_120376,RMVar_hsa_circ_185322,RMVar_hsa_circ_376410 97575 RMVar_ID_97575 Human_SNP_ID_626591833 m1A Human chr17 + 50368105 50368105 50368105 CGATGGCCTCAACAGGACATCAAAGCATAGCTACCAGTTTGAAGGTGCCCTCAGGCTTGGCAGGA CGATGGCCTCAACAGGACATCAAAGCATAGCTCCCAGTTTGAAGGTGCCCTCAGGCTTGGCAGGA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:50368005..50368105 26863410 MeRIP-seq:(Medium) rs943184997 Functional Loss SNV dbSNP153 33..33 33 - - - 97576 RMVar_ID_97576 Human_SNP_ID_626592446 m1A Human chr17 - 50370505 50370505 50370505 CGCATCCAAGAAGTCGGGTGGTAGCTCCAAAAACCTCGGTGGAAAGTCATCAGGCAGACGCCAAG CGCATCCAAGAAGTCGGGTGGTAGCTCCAAAATCCTCGGTGGAAAGTCATCAGGCAGACGCCAAG T A MRPL27 Ensembl:ENSG00000108826 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50370418..50370600 26863196 MeRIP-seq:(Medium) rs759861329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536797,Human_RBP_ID_4437528,Human_RBP_ID_9376331,Human_RBP_ID_13065569,Human_RBP_ID_22444753 Human_Splice_Rec_1837850,Human_Splice_Rec_1837851,Human_Splice_Rec_1837855,Human_Splice_Rec_1837860,Human_Splice_Rec_1837861,Human_Splice_Rec_1837866,Human_Splice_Rec_1837867,Human_Splice_Rec_1837874,Human_Splice_Rec_1837875,Human_Splice_Rec_1837878,Human_Splice_Rec_1837879,Human_Splice_Rec_1837884 RMVar_hsa_circ_114868,RMVar_hsa_circ_120376,RMVar_hsa_circ_185322,RMVar_hsa_circ_376410,RMVar_hsa_circ_185323 97577 RMVar_ID_97577 Human_SNP_ID_626592447 m1A Human chr17 - 50370505 50370505 50370505 CGCATCCAAGAAGTCGGGTGGTAGCTCCAAAAACCTCGGTGGAAAGTCATCAGGCAGACGCCAAG CGCATCCAAGAAGTCGGGTGGTAGCTCCAAAAGCCTCGGTGGAAAGTCATCAGGCAGACGCCAAG T C MRPL27 Ensembl:ENSG00000108826 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50370418..50370600 26863196 MeRIP-seq:(Medium) rs759861329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1536797,Human_RBP_ID_4437528,Human_RBP_ID_9376331,Human_RBP_ID_13065569,Human_RBP_ID_22444753 Human_Splice_Rec_1837850,Human_Splice_Rec_1837851,Human_Splice_Rec_1837855,Human_Splice_Rec_1837860,Human_Splice_Rec_1837861,Human_Splice_Rec_1837866,Human_Splice_Rec_1837867,Human_Splice_Rec_1837874,Human_Splice_Rec_1837875,Human_Splice_Rec_1837878,Human_Splice_Rec_1837879,Human_Splice_Rec_1837884 RMVar_hsa_circ_114868,RMVar_hsa_circ_120376,RMVar_hsa_circ_185322,RMVar_hsa_circ_376410,RMVar_hsa_circ_185323 97578 RMVar_ID_97578 Human_SNP_ID_626595777 m1A Human chr17 - 50382520 50382520 50382520 ACGCTCAGTAAATCCAGTCTAAACTGGGAGGTAGGGGTATTCCTGTTTTCTTTAGGACCTCAGAG ACGCTCAGTAAATCCAGTCTAAACTGGGAGGTCGGGGTATTCCTGTTTTCTTTAGGACCTCAGAG T G LRRC59 Ensembl:ENSG00000108829 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50382451..50382704 32194978 MeRIP-seq:(Medium) rs1298016618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1009068,Human_RBP_ID_1862204,Human_RBP_ID_3527795,Human_RBP_ID_4437634,Human_RBP_ID_6611237,Human_RBP_ID_17260638,Human_RBP_ID_17376361,Human_RBP_ID_17492185,Human_RBP_ID_17895644,Human_RBP_ID_18293745,Human_RBP_ID_18701963,Human_RBP_ID_22499815,Human_RBP_ID_27666584 RMVar_hsa_circ_113694,RMVar_hsa_circ_185326,RMVar_hsa_circ_89200,RMVar_hsa_circ_100239,RMVar_hsa_circ_185327,RMVar_hsa_circ_185328 97579 RMVar_ID_97579 Human_SNP_ID_626596518 m1A Human chr17 - 50385243 50385243 50385243 TGAGGCTAAGCAGCGAGCTAAGGAAGCTCAGGAGCGGGAACTGCGGAAGCGGGAGAAGGCGGAAG TGAGGCTAAGCAGCGAGCTAAGGAAGCTCAGGGGCGGGAACTGCGGAAGCGGGAGAAGGCGGAAG T C LRRC59 Ensembl:ENSG00000108829 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50385101..50385275 32194978 MeRIP-seq:(Medium) rs1183732756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47522,Human_RBP_ID_235424,Human_RBP_ID_764876,Human_RBP_ID_822527,Human_RBP_ID_5185327,Human_RBP_ID_6611278,Human_RBP_ID_9376338,Human_RBP_ID_20291966,Human_RBP_ID_22443062,Human_RBP_ID_22586412,Human_RBP_ID_22953779,Human_RBP_ID_23734096,Human_RBP_ID_26332052 Human_Splice_Rec_1837994 RMVar_hsa_circ_113694,RMVar_hsa_circ_185326,RMVar_hsa_circ_89200,RMVar_hsa_circ_100239,RMVar_hsa_circ_185327,RMVar_hsa_circ_185328,RMVar_hsa_circ_364413,RMVar_hsa_circ_365682 97580 RMVar_ID_97580 Human_SNP_ID_626596527 m1A Human chr17 - 50385279 50385277 50385280 TTTGGTATGTTTTGTTGTAGAGGCAGAGAAGAAGCGTGAGGCTAAGCAGCGAGCTAAGGAAGCTC TTTGGTATGTTTTGTTGTAGAGGCAGAGAAG___CGTGAGGCTAAGCAGCGAGCTAAGGAAGCTC GCTT G LRRC59 Ensembl:ENSG00000108829 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:50385068..50385342;chr17:50385079..50385326;chr17:50385069..50385342;chr17:50383200..50392500 26863196 MeRIP-seq:(Medium) rs756560115 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_47522,Human_RBP_ID_764876,Human_RBP_ID_822528,Human_RBP_ID_4437687,Human_RBP_ID_5115209,Human_RBP_ID_9376338,Human_RBP_ID_22445600,Human_RBP_ID_26332052 Human_Splice_Rec_1837994 RMVar_hsa_circ_113694,RMVar_hsa_circ_185326,RMVar_hsa_circ_89200,RMVar_hsa_circ_100239,RMVar_hsa_circ_185327,RMVar_hsa_circ_185328,RMVar_hsa_circ_364413,RMVar_hsa_circ_365682 97581 RMVar_ID_97581 Human_SNP_ID_626597140 m1A Human chr17 + 50388054 50388054 50388054 GGACCTGAAAGATAACTACAAGAGGGACAGCCACCTACCACGTTCTACTTCCAGCCGCCGCTGCC GGACCTGAAAGATAACTACAAGAGGGACAGCCCCCTACCACGTTCTACTTCCAGCCGCCGCTGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:50388051..50388150 26863196 MeRIP-seq:(Medium) rs1310338651 Functional Loss SNV dbSNP153 33..33 33 - - - 97582 RMVar_ID_97582 Human_SNP_ID_626599571 m1A Human chr17 - 50397463 50397463 50397463 TGGGAGCTAGGCGCGAGGCTCGGAGTGCGGCCAGCGGGCGGAGGCGGTCTCGCATCGGCGGCGAC TGGGAGCTAGGCGCGAGGCTCGGAGTGCGGCCGGCGGGCGGAGGCGGTCTCGCATCGGCGGCGAC T C LRRC59 Ensembl:ENSG00000108829 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:50397251..50397550 26863196 MeRIP-seq:(Medium) rs147909656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235947,Human_RBP_ID_764885,Human_RBP_ID_821913,Human_RBP_ID_4437723,Human_RBP_ID_5318477,Human_RBP_ID_9326743,Human_RBP_ID_22443788,Human_RBP_ID_22532982,Human_RBP_ID_22959853 RMVar_hsa_circ_89200,RMVar_hsa_circ_185328 97583 RMVar_ID_97583 Human_SNP_ID_626606740 m1A Human chr17 - 50426284 50426284 50426284 CCGAGCTCCCGGCGCACAGCCTCCCCAGGCGCAGCATCCCGACGTAGACAGCCATGGCTCGCTTT CCGAGCTCCCGGCGCACAGCCTCCCCAGGCGCGGCATCCCGACGTAGACAGCCATGGCTCGCTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:50426226..50426400;chr17:50426226..50426413;chr17:50426226..50426457;chr17:50426226..50426411 26863196 MeRIP-seq:(Medium) rs1224121331 Functional Loss SNV dbSNP153 33..33 33 - - - 97584 RMVar_ID_97584 Human_SNP_ID_626609297 m1A Human chr17 + 50437041 50437041 50437041 CACAAGCATTGGCCATCTCTACTCCCATATCAACGACCACTGGAAGGTCAACCACTAGCCTAGTG CACAAGCATTGGCCATCTCTACTCCCATATCAGCGACCACTGGAAGGTCAACCACTAGCCTAGTG A G ACSF2 Ensembl:ENSG00000167107 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50437038..50437245 26863196 MeRIP-seq:(Medium) rs937838139 Functional Loss SNV dbSNP153 33..33 33 - - - 97585 RMVar_ID_97585 Human_SNP_ID_626614895 m1A Human chr17 + 50461682 50461682 50461682 CTACCAGGCTATGGAACTGGAGTATGTCCTCAAGAAGGTACAGCTCATTTGTCGGGGAGGGGCCC CTACCAGGCTATGGAACTGGAGTATGTCCTCAGGAAGGTACAGCTCATTTGTCGGGGAGGGGCCC A G ACSF2 Ensembl:ENSG00000167107 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50461626..50462456 32194978 MeRIP-seq:(Medium) rs1453019114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23734182 Human_Splice_Rec_1838000,Human_Splice_Rec_1838001,Human_Splice_Rec_1838030,Human_Splice_Rec_1838031,Human_Splice_Rec_1838068,Human_Splice_Rec_1838069,Human_Splice_Rec_1838076,Human_Splice_Rec_1838077,Human_Splice_Rec_1838108,Human_Splice_Rec_1838109,Human_Splice_Rec_1838137 RMVar_hsa_circ_88363,RMVar_hsa_circ_185331 97586 RMVar_ID_97586 Human_SNP_ID_626614896 m1A Human chr17 + 50461682 50461682 50461682 CTACCAGGCTATGGAACTGGAGTATGTCCTCAAGAAGGTACAGCTCATTTGTCGGGGAGGGGCCC CTACCAGGCTATGGAACTGGAGTATGTCCTCATGAAGGTACAGCTCATTTGTCGGGGAGGGGCCC A T ACSF2 Ensembl:ENSG00000167107 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50461626..50462456 32194978 MeRIP-seq:(Medium) rs1453019114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23734182 Human_Splice_Rec_1838000,Human_Splice_Rec_1838001,Human_Splice_Rec_1838030,Human_Splice_Rec_1838031,Human_Splice_Rec_1838068,Human_Splice_Rec_1838069,Human_Splice_Rec_1838076,Human_Splice_Rec_1838077,Human_Splice_Rec_1838108,Human_Splice_Rec_1838109,Human_Splice_Rec_1838137 RMVar_hsa_circ_88363,RMVar_hsa_circ_185331 97587 RMVar_ID_97587 Human_SNP_ID_626615503 m1A Human chr17 + 50463461 50463461 50463461 CCCTGTACCATTGCCTGGGTTCCGTGGCAGGCACAATGATGTGTCTGATGTACGGTGCCACCCTC CCCTGTACCATTGCCTGGGTTCCGTGGCAGGCGCAATGATGTGTCTGATGTACGGTGCCACCCTC A G ACSF2 Ensembl:ENSG00000167107 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50463151..50463550 32194978 MeRIP-seq:(Medium) rs1241692777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376348,Human_RBP_ID_18988789,Human_RBP_ID_22444764 Human_Splice_Rec_1838008,Human_Splice_Rec_1838009,Human_Splice_Rec_1838038,Human_Splice_Rec_1838039,Human_Splice_Rec_1838084,Human_Splice_Rec_1838085,Human_Splice_Rec_1838116,Human_Splice_Rec_1838117,Human_Splice_Rec_1838144,Human_Splice_Rec_1838145,Human_Splice_Rec_1838168,Human_Splice_Rec_1838169,Human_Splice_Rec_1838175,Human_Splice_Rec_1838187 RMVar_hsa_circ_29250,RMVar_hsa_circ_88363,RMVar_hsa_circ_185331,RMVar_hsa_circ_94044,RMVar_hsa_circ_185333 97588 RMVar_ID_97588 Human_SNP_ID_626617783 m1A Human chr17 + 50471128 50471128 50471128 GAAGGCAGAAAGCGTGGGCAGAATTATGCCTCACACGGAGGTGAGCCCCTGACCAAGACTCCAAA GAAGGCAGAAAGCGTGGGCAGAATTATGCCTCGCACGGAGGTGAGCCCCTGACCAAGACTCCAAA A G ACSF2 Ensembl:ENSG00000167107 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50471077..50471178 32194978 MeRIP-seq:(Medium) rs766753294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26330799 Human_Splice_Rec_1838015,Human_Splice_Rec_1838045,Human_Splice_Rec_1838091,Human_Splice_Rec_1838123,Human_Splice_Rec_1838151,Human_Splice_Rec_1838181,Human_Splice_Rec_1838195,Human_Splice_Rec_1838207,Human_Splice_Rec_1838215,Human_Splice_Rec_1838231,Human_Splice_Rec_1838237 RMVar_hsa_circ_94044,RMVar_hsa_circ_123603,RMVar_hsa_circ_185333,RMVar_hsa_circ_185334 97589 RMVar_ID_97589 Human_SNP_ID_626620695 m1A Human chr17 + 50482198 50482192 50482198 GCCCGGCGCCTCTTTCCCGGGCGCGTGTCTGTAGACTTGATGCTGGGGCTGCCGGCACAGCAGGT GCCCGGCGCCTCTTTCCCGGGCGCGTG______GACTTGATGCTGGGGCTGCCGGCACAGCAGGT GTCTGTA G RSAD1 Ensembl:ENSG00000136444 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1433653470 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_5367435,Human_RBP_ID_22588346 RMVar_hsa_circ_100390,RMVar_hsa_circ_91057,RMVar_hsa_circ_185337,RMVar_hsa_circ_185338 97590 RMVar_ID_97590 Human_SNP_ID_626620696 m1A Human chr17 + 50482198 50482198 50482198 GCCCGGCGCCTCTTTCCCGGGCGCGTGTCTGTAGACTTGATGCTGGGGCTGCCGGCACAGCAGGT GCCCGGCGCCTCTTTCCCGGGCGCGTGTCTGTGGACTTGATGCTGGGGCTGCCGGCACAGCAGGT A G RSAD1 Ensembl:ENSG00000136444 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7210579 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5367435,Human_RBP_ID_22588346 RMVar_hsa_circ_100390,RMVar_hsa_circ_91057,RMVar_hsa_circ_185337,RMVar_hsa_circ_185338 97591 RMVar_ID_97591 Human_SNP_ID_626637488 m1A Human chr17 + 50541618 50541618 50541618 TGCCGGACTCCCGAGTCCTTCCTGGGTCCCTCAGCTTCCTCCTTGGTCAACCTTGACTCGTTGGT TGCCGGACTCCCGAGTCCTTCCTGGGTCCCTCGGCTTCCTCCTTGGTCAACCTTGACTCGTTGGT A G EPN3 Ensembl:ENSG00000049283 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50541616..50541874 26863196 MeRIP-seq:(Medium) rs763507290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1838571,Human_Splice_Rec_1838599,Human_Splice_Rec_1838617,Human_Splice_Rec_1838631,Human_Splice_Rec_1838667,Human_Splice_Rec_1838683 97592 RMVar_ID_97592 Human_SNP_ID_626637693 m1A Human chr17 - 50542022 50542022 50542022 AAGACGCTAACCGAGGCGGGGAGGGTCAAGCCAGCTGGCACGCTGCTGAGCGGGAGGGGCAGAGA AAGACGCTAACCGAGGCGGGGAGGGTCAAGCCGGCTGGCACGCTGCTGAGCGGGAGGGGCAGAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:50542006..50542102 26863196 MeRIP-seq:(Medium) rs1235413566 Functional Loss SNV dbSNP153 33..33 33 - - - 97593 RMVar_ID_97593 Human_SNP_ID_626639073 m1A Human chr17 - 50547249 50547249 50547249 GGCTCGCGGCGAGGCCTGCACCGGCGCGGGGCAGCAGAAGGACGCGGCCCAACCAGGCCCGCGCG GGCTCGCGGCGAGGCCTGCACCGGCGCGGGGCGGCAGAAGGACGCGGCCCAACCAGGCCCGCGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50547205..50547294 26863196 MeRIP-seq:(Medium) rs967349977 Functional Loss SNV dbSNP153 33..33 33 - - - 97594 RMVar_ID_97594 Human_SNP_ID_626639464 m1A Human chr17 - 50548343 50548343 50548343 GTAGATGAAGGATGGCTTCCTTTCCCTCCAGCAGGCATGGGCACTGAACTACTGACCGTCGCACT GTAGATGAAGGATGGCTTCCTTTCCCTCCAGCTGGCATGGGCACTGAACTACTGACCGTCGCACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50548294..50548392 26863196 MeRIP-seq:(Medium) rs904739918 Functional Loss SNV dbSNP153 33..33 33 - - - 97595 RMVar_ID_97595 Human_SNP_ID_626640137 m1A Human chr17 + 50550033 50550033 50550033 GTTCTCCTACTGGCTCAGCCATCGACTGACTCAGGATGGCTCTCGGGCCCAGCAGATGGCCTTGC GTTCTCCTACTGGCTCAGCCATCGACTGACTCCGGATGGCTCTCGGGCCCAGCAGATGGCCTTGC A C SPATA20 Ensembl:ENSG00000006282 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50549976..50550075 32194978 MeRIP-seq:(Medium) rs756986400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376358,Human_RBP_ID_18988805 Human_Splice_Rec_1838702,Human_Splice_Rec_1838728,Human_Splice_Rec_1838729,Human_Splice_Rec_1838758,Human_Splice_Rec_1838759,Human_Splice_Rec_1838790,Human_Splice_Rec_1838791,Human_Splice_Rec_1838846,Human_Splice_Rec_1838847,Human_Splice_Rec_1838894,Human_Splice_Rec_1838916,Human_Splice_Rec_1838917,Human_Splice_Rec_1838946,Human_Splice_Rec_1838947,Human_Splice_Rec_1838970,Human_Splice_Rec_1838986,Human_Splice_Rec_1838987,Human_Splice_Rec_1839020,Human_Splice_Rec_1839021,Human_Splice_Rec_1839042,Human_Splice_Rec_1839043,Human_Splice_Rec_1839056 RMVar_hsa_circ_9223,RMVar_hsa_circ_85716,RMVar_hsa_circ_80069,RMVar_hsa_circ_97053,RMVar_hsa_circ_185343,RMVar_hsa_circ_185345,RMVar_hsa_circ_76218,RMVar_hsa_circ_185346,RMVar_hsa_circ_185344,RMVar_hsa_circ_185347,RMVar_hsa_circ_89060 97596 RMVar_ID_97596 Human_SNP_ID_626667524 m1A Human chr17 + 50649737 50649729 50649737 AAGGGAAAGAAAGAAGGAAGGAAGGAAGGAAGAAAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA AAGGGAAAGAAAGAAGGAAGGAAGG________AAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA GAAGGAAGA G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50649735..50649800 26863196 MeRIP-seq:(Medium) rs1168334286 Functional Loss DEL dbSNP153 26..33 33 - - - 97597 RMVar_ID_97597 Human_SNP_ID_626667526 m1A Human chr17 + 50649737 50649733 50649737 AAGGGAAAGAAAGAAGGAAGGAAGGAAGGAAGAAAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA AAGGGAAAGAAAGAAGGAAGGAAGGAAGG____AAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA GAAGA G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50649735..50649800 26863196 MeRIP-seq:(Medium) rs1238075345 Functional Loss DEL dbSNP153 30..33 33 - - - 97598 RMVar_ID_97598 Human_SNP_ID_626667527 m1A Human chr17 + 50649737 50649737 50649737 AAGGGAAAGAAAGAAGGAAGGAAGGAAGGAAGAAAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA AAGGGAAAGAAAGAAGGAAGGAAGGAAGGAAGGAAGAGAGAGAGAGAAAGGAAGGAAGGAAGGAA A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50649735..50649800 26863196 MeRIP-seq:(Medium) rs192887672 Functional Loss SNV dbSNP153 33..33 33 - - - 97599 RMVar_ID_97599 Human_SNP_ID_626669403 m1A Human chr17 - 50656885 50656885 50656885 GCCCTCTCCTCAGAGCCCACAGTTTCCCTATCACAGTCCACAACCCAATGGAGACCTCCCCCATC GCCCTCTCCTCAGAGCCCACAGTTTCCCTATCGCAGTCCACAACCCAATGGAGACCTCCCCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:50656835..50656928 26863196 MeRIP-seq:(Medium) rs1021639883 Functional Loss SNV dbSNP153 33..33 33 - - - 97600 RMVar_ID_97600 Human_SNP_ID_626670807 m1A Human chr17 + 50662084 50662084 50662084 AGATCTGAGCCAGGGAGGGGCATCTGGCTTCAAGGATCTCCTGCCAGGAGTGTGGGGGATGTAGG AGATCTGAGCCAGGGAGGGGCATCTGGCTTCAGGGATCTCCTGCCAGGAGTGTGGGGGATGTAGG A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:50662072..50662197 26863196 MeRIP-seq:(Medium) rs955199726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360320,RMVar_hsa_circ_317054,RMVar_hsa_circ_185354,RMVar_hsa_circ_92248,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_114819,RMVar_hsa_circ_94020,RMVar_hsa_circ_185356,RMVar_hsa_circ_185358,RMVar_hsa_circ_185360,RMVar_hsa_circ_77904,RMVar_hsa_circ_185361,RMVar_hsa_circ_185359,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362 97601 RMVar_ID_97601 Human_SNP_ID_626670827 m1A Human chr17 - 50662182 50662182 50662182 GCACACGCCCATCTCCCAAATTGCTCCTGAATACTTGTCTCATTCCTGGCCTGGACTCCATCTGA GCACACGCCCATCTCCCAAATTGCTCCTGAATGCTTGTCTCATTCCTGGCCTGGACTCCATCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50661953..50662339 26863196 MeRIP-seq:(Medium) rs7216383 Functional Loss SNV dbSNP153 33..33 33 - - - 97602 RMVar_ID_97602 Human_SNP_ID_626671159 m1A Human chr17 + 50663374 50663373 50663374 GAGCAGGGAAGTCCAGTCAATGGAAACGTGGCATTTCTTCCCGCCATATGTCAGGAGGTAAGAAG GAGCAGGGAAGTCCAGTCAATGGAAACGTGGC_TTTCTTCCCGCCATATGTCAGGAGGTAAGAAG CA C ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50663340..50663494 26863196 MeRIP-seq:(Medium) rs1215936524 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_360320,RMVar_hsa_circ_317054,RMVar_hsa_circ_185354,RMVar_hsa_circ_92248,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_114819,RMVar_hsa_circ_94020,RMVar_hsa_circ_185356,RMVar_hsa_circ_185358,RMVar_hsa_circ_185360,RMVar_hsa_circ_77904,RMVar_hsa_circ_185361,RMVar_hsa_circ_185359,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362 97603 RMVar_ID_97603 Human_SNP_ID_626671160 m1A Human chr17 + 50663374 50663374 50663374 GAGCAGGGAAGTCCAGTCAATGGAAACGTGGCATTTCTTCCCGCCATATGTCAGGAGGTAAGAAG GAGCAGGGAAGTCCAGTCAATGGAAACGTGGCGTTTCTTCCCGCCATATGTCAGGAGGTAAGAAG A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50663340..50663494 26863196 MeRIP-seq:(Medium) rs900977893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360320,RMVar_hsa_circ_317054,RMVar_hsa_circ_185354,RMVar_hsa_circ_92248,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_114819,RMVar_hsa_circ_94020,RMVar_hsa_circ_185356,RMVar_hsa_circ_185358,RMVar_hsa_circ_185360,RMVar_hsa_circ_77904,RMVar_hsa_circ_185361,RMVar_hsa_circ_185359,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362 97604 RMVar_ID_97604 Human_SNP_ID_626671161 m1A Human chr17 + 50663374 50663374 50663374 GAGCAGGGAAGTCCAGTCAATGGAAACGTGGCATTTCTTCCCGCCATATGTCAGGAGGTAAGAAG GAGCAGGGAAGTCCAGTCAATGGAAACGTGGCTTTTCTTCCCGCCATATGTCAGGAGGTAAGAAG A T ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:50663340..50663494 26863196 MeRIP-seq:(Medium) rs900977893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360320,RMVar_hsa_circ_317054,RMVar_hsa_circ_185354,RMVar_hsa_circ_92248,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_114819,RMVar_hsa_circ_94020,RMVar_hsa_circ_185356,RMVar_hsa_circ_185358,RMVar_hsa_circ_185360,RMVar_hsa_circ_77904,RMVar_hsa_circ_185361,RMVar_hsa_circ_185359,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362 97605 RMVar_ID_97605 Human_SNP_ID_626683266 m1A Human chr17 - 50707819 50707819 50707819 GCCGGGAGCAGCAGGGGCGGCCCGCGGGAGGGAGCGGAAGTCCCGGGGCGGGCGCGGGCAGCGGC GCCGGGAGCAGCAGGGGCGGCCCGCGGGAGGGGGCGGAAGTCCCGGGGCGGGCGCGGGCAGCGGC T C ANKRD40 Ensembl:ENSG00000154945 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50707498..50707893 26863196 MeRIP-seq:(Medium) rs1402217808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236481,Human_RBP_ID_822305,Human_RBP_ID_4464668,Human_RBP_ID_9422394,Human_RBP_ID_18420019 RMVar_hsa_circ_88427,RMVar_hsa_circ_185373 97606 RMVar_ID_97606 Human_SNP_ID_626686367 m1A Human chr17 - 50719659 50719659 50719659 CGCCAACGAAAACACGGGCGACACCGTCGCCAATCTCCTCGGCCCGCTCTCAGGCCGAAATCCCT CGCCAACGAAAACACGGGCGACACCGTCGCCAGTCTCCTCGGCCCGCTCTCAGGCCGAAATCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:50719593..50722724;chr17:50719601..50719936;chr17:50719576..50722724;chr17:50719576..50719850 26863196 MeRIP-seq:(Medium) rs953784011 Functional Loss SNV dbSNP153 33..33 33 - - - 97607 RMVar_ID_97607 Human_SNP_ID_626686405 m1A Human chr17 + 50719726 50719726 50719726 TGCCTGGGCTGGTGGGAACAGCCGCCCGAAGGAAGCACCATGATTTCGGCCGCGCAGTTGTTGGA TGCCTGGGCTGGTGGGAACAGCCGCCCGAAGGGAGCACCATGATTTCGGCCGCGCAGTTGTTGGA A G LUC7L3 Ensembl:ENSG00000108848 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:50719639..50719737;chr17:50719626..50719850 26863410 MeRIP-seq:(Medium) rs1451713897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237694,Human_RBP_ID_493546,Human_RBP_ID_768292,Human_RBP_ID_1536995,Human_RBP_ID_1862327,Human_RBP_ID_3950851,Human_RBP_ID_4467293,Human_RBP_ID_5185919,Human_RBP_ID_6611677,Human_RBP_ID_8456561,Human_RBP_ID_9326745,Human_RBP_ID_9376369,Human_RBP_ID_13067332,Human_RBP_ID_17895794,Human_RBP_ID_18419655,Human_RBP_ID_18702134,Human_RBP_ID_22061512,Human_RBP_ID_22959625,Human_RBP_ID_24544891,Human_RBP_ID_25344098,Human_RBP_ID_26333567,Human_RBP_ID_27812861 97608 RMVar_ID_97608 Human_SNP_ID_626686407 m1A Human chr17 + 50719730 50719730 50719730 TGGGCTGGTGGGAACAGCCGCCCGAAGGAAGCACCATGATTTCGGCCGCGCAGTTGTTGGATGAG TGGGCTGGTGGGAACAGCCGCCCGAAGGAAGCGCCATGATTTCGGCCGCGCAGTTGTTGGATGAG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50719601..50719801 26863196 MeRIP-seq:(Medium) rs759220436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493546,Human_RBP_ID_768292,Human_RBP_ID_1536995,Human_RBP_ID_1862327,Human_RBP_ID_3950851,Human_RBP_ID_4467293,Human_RBP_ID_5185919,Human_RBP_ID_6611677,Human_RBP_ID_8456561,Human_RBP_ID_9326745,Human_RBP_ID_9376369,Human_RBP_ID_13067332,Human_RBP_ID_17895794,Human_RBP_ID_18419655,Human_RBP_ID_18702134,Human_RBP_ID_22061512,Human_RBP_ID_22959625,Human_RBP_ID_24544891,Human_RBP_ID_25344098,Human_RBP_ID_26333567,Human_RBP_ID_27812861 97609 RMVar_ID_97609 Human_SNP_ID_626691902 m1A Human chr17 - 50736929 50736929 50736929 ACCTAGTAAAGAAAAACAAAGGTACTTAAAAAATTGCTTGGTTTTAAAACTTTATTGGAGAAAGG ACCTAGTAAAGAAAAACAAAGGTACTTAAAAATTTGCTTGGTTTTAAAACTTTATTGGAGAAAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50736926..50737068 26863196 MeRIP-seq:(Medium) rs1157393718 Functional Loss SNV dbSNP153 33..33 33 - - - 97610 RMVar_ID_97610 Human_SNP_ID_626692019 m1A Human chr17 - 50737329 50737329 50737329 GCTACTCCTCCATCCACTTGTCATCTTCCAAAAATTTGCTGACATCTCTAATGTTATCTCCTCTT GCTACTCCTCCATCCACTTGTCATCTTCCAAAGATTTGCTGACATCTCTAATGTTATCTCCTCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50737326..50737436 26863196 MeRIP-seq:(Medium) rs1467767077 Functional Loss SNV dbSNP153 33..33 33 - - - 97611 RMVar_ID_97611 Human_SNP_ID_626692570 m1A Human chr17 - 50739480 50739480 50739480 CTGCGTAATTTTTTTGTATTTTTAGTAGAGACAGGATTTCACCCTGTTGGGCAAGCTGTTCTTGA CTGCGTAATTTTTTTGTATTTTTAGTAGAGACGGGATTTCACCCTGTTGGGCAAGCTGTTCTTGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:50739477..50739670 26863196 MeRIP-seq:(Medium) rs372125471 Functional Loss SNV dbSNP153 33..33 33 - - - 97612 RMVar_ID_97612 Human_SNP_ID_626694407 m1A Human chr17 + 50745838 50745838 50745838 ACGGGAGAGAGAAAGGGAAGAAAGAGAAAGGAAAAGACGAAGGGAAGAGGAAGAAAGAGAAAAAG ACGGGAGAGAGAAAGGGAAGAAAGAGAAAGGAGAAGACGAAGGGAAGAGGAAGAAAGAGAAAAAG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:50744726..50749243 26863196 MeRIP-seq:(Medium) rs1415897600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_201599,Human_RBP_ID_235953,Human_RBP_ID_821811,Human_RBP_ID_900344,Human_RBP_ID_1546663,Human_RBP_ID_2512103,Human_RBP_ID_5577526,Human_RBP_ID_9867260,Human_RBP_ID_18412050,Human_RBP_ID_22740564,Human_RBP_ID_22953891,Human_RBP_ID_23114419,Human_RBP_ID_23118770,Human_RBP_ID_24544907,Human_RBP_ID_24552312,Human_RBP_ID_25299468,Human_RBP_ID_26332065,Human_RBP_ID_27814048 RMVar_hsa_circ_355377,RMVar_hsa_circ_351997,RMVar_hsa_circ_119164,RMVar_hsa_circ_185379,RMVar_hsa_circ_95995,RMVar_hsa_circ_368830,RMVar_hsa_circ_185380 97613 RMVar_ID_97613 Human_SNP_ID_626694645 m1A Human chr17 + 50746640 50746640 50746640 GGATCGAAGAAGATCAAAAAGCCGGGATCGAAAGTCATATAAGCACAGGAGCAAAAGTCGGGACA GGATCGAAGAAGATCAAAAAGCCGGGATCGAAGGTCATATAAGCACAGGAGCAAAAGTCGGGACA A G LUC7L3 Ensembl:ENSG00000108848 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50743773..50748391 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_493556,Human_RBP_ID_900348,Human_RBP_ID_1546666,Human_RBP_ID_1862403,Human_RBP_ID_2512116,Human_RBP_ID_5577535,Human_RBP_ID_6611974,Human_RBP_ID_13068254,Human_RBP_ID_17653874,Human_RBP_ID_18411908,Human_RBP_ID_18991808,Human_RBP_ID_22805543,Human_RBP_ID_22959240,Human_RBP_ID_23114379,Human_RBP_ID_24544914,Human_RBP_ID_25344151,Human_RBP_ID_26332068,Human_RBP_ID_27812878 Human_Splice_Rec_1841608,Human_Splice_Rec_1841609,Human_Splice_Rec_1841628,Human_Splice_Rec_1841629,Human_Splice_Rec_1841648,Human_Splice_Rec_1841649,Human_Splice_Rec_1841674,Human_Splice_Rec_1841675,Human_Splice_Rec_1841718,Human_Splice_Rec_1841719,Human_Splice_Rec_1841724,Human_Splice_Rec_1841725,Human_Splice_Rec_1841729,Human_Splice_Rec_1841733,Human_Splice_Rec_1841739 Human_miRNA_ID_2237646,Human_miRNA_ID_2237647 RMVar_hsa_circ_355377,RMVar_hsa_circ_351997,RMVar_hsa_circ_119164,RMVar_hsa_circ_185379,RMVar_hsa_circ_95995,RMVar_hsa_circ_368830,RMVar_hsa_circ_85549,RMVar_hsa_circ_185380,RMVar_hsa_circ_185381 97614 RMVar_ID_97614 Human_SNP_ID_626696051 m1A Human chr17 - 50752330 50752330 50752330 CATCAGTCCTGAATTAACTTTTAATAATAATAATAATAAAAAAACTAACTGAGCTTTATACTTTT CATCAGTCCTGAATTAACTTTTAATAATAATAGTAATAAAAAAACTAACTGAGCTTTATACTTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50752286..50752386 32194978 MeRIP-seq:(Medium) rs1467792926 Functional Loss SNV dbSNP153 33..33 33 - - - 97615 RMVar_ID_97615 Human_SNP_ID_626725122 m1A Human chr17 - 50863298 50863293 50863299 TATGGGCTTGGCTTGGGTAGCCAGCAGCAGCCACAGCAACAGCAGCAGCCAGCCCAGCCGCCACC TATGGGCTTGGCTTGGGTAGCCAGCAGCAGC______AACAGCAGCAGCCAGCCCAGCCGCCACC TGCTGTG T TOB1 Ensembl:ENSG00000141232 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:50863248..50863369 26863196 MeRIP-seq:(Medium) rs1223953054 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_5144258,Human_RBP_ID_17264036,Human_RBP_ID_22061513,Human_RBP_ID_27256780 97616 RMVar_ID_97616 Human_SNP_ID_626725205 m1A Human chr17 + 50863547 50863546 50863547 ATGAAGGTAGGGCTTACAGCAGCAGAGTGACCAAAAGGAGGCGATGGAGAGCTGGACACTGATGA ATGAAGGTAGGGCTTACAGCAGCAGAGTGACC_AAAGGAGGCGATGGAGAGCTGGACACTGATGA CA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:50863501..50863575 26863196 MeRIP-seq:(Medium) rs1318084514 Functional Loss DEL dbSNP153 33..33 33 - - - 97617 RMVar_ID_97617 Human_SNP_ID_626725951 m1A Human chr17 - 50866293 50866293 50866293 AGCGGGCGCACTACGGGGACGCTGGGCCGGGCACCGGGCTGTGTGGAGAAGTGAGCGCGCTCGTC AGCGGGCGCACTACGGGGACGCTGGGCCGGGCGCCGGGCTGTGTGGAGAAGTGAGCGCGCTCGTC T C TOB1 Ensembl:ENSG00000141232 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:50865637..50866350;chr17:50866123..50866325;chr17:50865685..50866350 26863196 MeRIP-seq:(Medium) rs1478069006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464671,Human_RBP_ID_5144263,Human_RBP_ID_5466686,Human_RBP_ID_5497346,Human_RBP_ID_6612387,Human_RBP_ID_24479747 97618 RMVar_ID_97618 Human_SNP_ID_626726162 m1A Human chr17 - 50866827 50866827 50866827 GCAGACCCCCGCGGAGAGGGCACTTTCTGGGTACTCTTGCCGCTCCTCCAGCCCCGGTTCTCCTG GCAGACCCCCGCGGAGAGGGCACTTTCTGGGTGCTCTTGCCGCTCCTCCAGCCCCGGTTCTCCTG T C TOB1 Ensembl:ENSG00000141232 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50866777..50866906 26863196 MeRIP-seq:(Medium) rs536560118 Functional Loss SNV dbSNP153 33..33 33 - - - 97619 RMVar_ID_97619 Human_SNP_ID_626750409 m1A Human chr17 - 50964505 50964505 50964505 CAGCTCACTGCAACCTCCACCTCTCAGGTTCAAGTAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAACCTCCACCTCTCAGGTTCATGTAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT T A SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs955026114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 97620 RMVar_ID_97620 Human_SNP_ID_626750824 m1A Human chr17 - 50966280 50966280 50966280 GTCACTTGATAGTGTGGCAAGTGATGTATGGCAATGAGTGAGCCCATGGGAAACAGGTGGAGATG GTCACTTGATAGTGTGGCAAGTGATGTATGGCTATGAGTGAGCCCATGGGAAACAGGTGGAGATG T A SPAG9 Ensembl:ENSG00000008294 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50966101..50966400 32194978 MeRIP-seq:(Medium) rs1373355878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493685,Human_RBP_ID_4438542,Human_RBP_ID_8819726,Human_RBP_ID_13069257,Human_RBP_ID_20234912,Human_RBP_ID_23210039,Human_RBP_ID_23734636 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 97621 RMVar_ID_97621 Human_SNP_ID_626754682 m1A Human chr17 - 50982672 50982672 50982672 GTATTTACTATAACCTTTTATTTTTTTTAAAGATGGGCAGTGGGATTTGTCAAACTATCACCTCT GTATTTACTATAACCTTTTATTTTTTTTAAAGGTGGGCAGTGGGATTTGTCAAACTATCACCTCT T C SPAG9 Ensembl:ENSG00000008294 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50982651..50982675 32194978 MeRIP-seq:(Medium) rs774895860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238854,Human_RBP_ID_6612546 Human_Splice_Rec_1841862,Human_Splice_Rec_1841918,Human_Splice_Rec_1841968,Human_Splice_Rec_1842026,Human_Splice_Rec_1842080 RMVar_hsa_circ_127939,RMVar_hsa_circ_121797,RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_338882,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388,RMVar_hsa_circ_315117,RMVar_hsa_circ_335693,RMVar_hsa_circ_271034,RMVar_hsa_circ_185394,RMVar_hsa_circ_86087,RMVar_hsa_circ_119861,RMVar_hsa_circ_185396,RMVar_hsa_circ_76416,RMVar_hsa_circ_185395,RMVar_hsa_circ_185392,RMVar_hsa_circ_185393,RMVar_hsa_circ_340441,RMVar_hsa_circ_370119,RMVar_hsa_circ_346416,RMVar_hsa_circ_325249,RMVar_hsa_circ_55008,RMVar_hsa_circ_185398,RMVar_hsa_circ_21041,RMVar_hsa_circ_185397,RMVar_hsa_circ_272376,RMVar_hsa_circ_305558,RMVar_hsa_circ_371422,RMVar_hsa_circ_32589,RMVar_hsa_circ_357468,RMVar_hsa_circ_278996,RMVar_hsa_circ_100867,RMVar_hsa_circ_271489,RMVar_hsa_circ_59017,RMVar_hsa_circ_185401,RMVar_hsa_circ_185403,RMVar_hsa_circ_185404,RMVar_hsa_circ_185405,RMVar_hsa_circ_185402,RMVar_hsa_circ_321177,RMVar_hsa_circ_185400,RMVar_hsa_circ_340366,RMVar_hsa_circ_344516,RMVar_hsa_circ_271022,RMVar_hsa_circ_309391,RMVar_hsa_circ_270850,RMVar_hsa_circ_185410,RMVar_hsa_circ_71819,RMVar_hsa_circ_77350,RMVar_hsa_circ_18177,RMVar_hsa_circ_185411,RMVar_hsa_circ_185408,RMVar_hsa_circ_185409,RMVar_hsa_circ_185407 97622 RMVar_ID_97622 Human_SNP_ID_626754683 m1A Human chr17 - 50982672 50982672 50982672 GTATTTACTATAACCTTTTATTTTTTTTAAAGATGGGCAGTGGGATTTGTCAAACTATCACCTCT GTATTTACTATAACCTTTTATTTTTTTTAAAGCTGGGCAGTGGGATTTGTCAAACTATCACCTCT T G SPAG9 Ensembl:ENSG00000008294 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50982651..50982675 32194978 MeRIP-seq:(Medium) rs774895860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238854,Human_RBP_ID_6612546 Human_Splice_Rec_1841862,Human_Splice_Rec_1841918,Human_Splice_Rec_1841968,Human_Splice_Rec_1842026,Human_Splice_Rec_1842080 RMVar_hsa_circ_127939,RMVar_hsa_circ_121797,RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_338882,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388,RMVar_hsa_circ_315117,RMVar_hsa_circ_335693,RMVar_hsa_circ_271034,RMVar_hsa_circ_185394,RMVar_hsa_circ_86087,RMVar_hsa_circ_119861,RMVar_hsa_circ_185396,RMVar_hsa_circ_76416,RMVar_hsa_circ_185395,RMVar_hsa_circ_185392,RMVar_hsa_circ_185393,RMVar_hsa_circ_340441,RMVar_hsa_circ_370119,RMVar_hsa_circ_346416,RMVar_hsa_circ_325249,RMVar_hsa_circ_55008,RMVar_hsa_circ_185398,RMVar_hsa_circ_21041,RMVar_hsa_circ_185397,RMVar_hsa_circ_272376,RMVar_hsa_circ_305558,RMVar_hsa_circ_371422,RMVar_hsa_circ_32589,RMVar_hsa_circ_357468,RMVar_hsa_circ_278996,RMVar_hsa_circ_100867,RMVar_hsa_circ_271489,RMVar_hsa_circ_59017,RMVar_hsa_circ_185401,RMVar_hsa_circ_185403,RMVar_hsa_circ_185404,RMVar_hsa_circ_185405,RMVar_hsa_circ_185402,RMVar_hsa_circ_321177,RMVar_hsa_circ_185400,RMVar_hsa_circ_340366,RMVar_hsa_circ_344516,RMVar_hsa_circ_271022,RMVar_hsa_circ_309391,RMVar_hsa_circ_270850,RMVar_hsa_circ_185410,RMVar_hsa_circ_71819,RMVar_hsa_circ_77350,RMVar_hsa_circ_18177,RMVar_hsa_circ_185411,RMVar_hsa_circ_185408,RMVar_hsa_circ_185409,RMVar_hsa_circ_185407 97623 RMVar_ID_97623 Human_SNP_ID_626760466 m1A Human chr17 - 51006201 51006201 51006201 GCTTTGAACATAGTGAAGAATGATTTGATAGCAAAAGTGGATGAACTGACCTGTGAGAAAGATGT GCTTTGAACATAGTGAAGAATGATTTGATAGCGAAAGTGGATGAACTGACCTGTGAGAAAGATGT T C SPAG9 Ensembl:ENSG00000008294 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:51006151..51006200 32194978 MeRIP-seq:(Medium) rs941734965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46714,Human_RBP_ID_1862631,Human_RBP_ID_3952691,Human_RBP_ID_4438679,Human_RBP_ID_18702369,Human_RBP_ID_23734721,Human_RBP_ID_26332086,Human_RBP_ID_27812899 Human_Splice_Rec_1841836,Human_Splice_Rec_1841890,Human_Splice_Rec_1841940,Human_Splice_Rec_1841996,Human_Splice_Rec_1842052,Human_Splice_Rec_1842128,Human_Splice_Rec_1842164,Human_Splice_Rec_1842206,Human_Splice_Rec_1842220 Human_miRNA_ID_1000820,Human_miRNA_ID_2245805,Human_miRNA_ID_2245806 RMVar_hsa_circ_6656,RMVar_hsa_circ_21041,RMVar_hsa_circ_71819,RMVar_hsa_circ_77350,RMVar_hsa_circ_185407,RMVar_hsa_circ_366224,RMVar_hsa_circ_93133,RMVar_hsa_circ_185418,RMVar_hsa_circ_348546,RMVar_hsa_circ_42517,RMVar_hsa_circ_67403,RMVar_hsa_circ_14641,RMVar_hsa_circ_32887,RMVar_hsa_circ_62907,RMVar_hsa_circ_47742,RMVar_hsa_circ_34561,RMVar_hsa_circ_98563,RMVar_hsa_circ_72994,RMVar_hsa_circ_376990,RMVar_hsa_circ_50435,RMVar_hsa_circ_5212,RMVar_hsa_circ_13090,RMVar_hsa_circ_185426 97624 RMVar_ID_97624 Human_SNP_ID_626789824 m1A Human chr17 + 51120719 51120719 51120719 GCGTCGCCGGCAGAGGGGCGGCACCTGCCCGCACGGGACGGACCCGACTCGGGCTGGGACGGGTA GCGTCGCCGGCAGAGGGGCGGCACCTGCCCGCCCGGGACGGACCCGACTCGGGCTGGGACGGGTA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:51120612..51120796 26863196 MeRIP-seq:(Medium) rs1051360942 Functional Loss SNV dbSNP153 33..33 33 - - - 97625 RMVar_ID_97625 Human_SNP_ID_626789868 m1A Human chr17 - 51120826 51120826 51120826 GCAGCGGCGGTTGGGGTGAGAGCGCCTACGCCACCCCTCCCCTCCTCCGGCCCCGGCCCCCACCC GCAGCGGCGGTTGGGGTGAGAGCGCCTACGCCCCCCCTCCCCTCCTCCGGCCCCGGCCCCCACCC T G SPAG9 Ensembl:ENSG00000008294 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:51120726..51120875 26863410 MeRIP-seq:(Medium) rs930281401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465537,Human_RBP_ID_8824838,Human_RBP_ID_9378572,Human_RBP_ID_18419658 RMVar_hsa_circ_266744 97626 RMVar_ID_97626 Human_SNP_ID_626798489 m1A Human chr17 - 51153622 51153622 51153622 CTGCTTAGGTTTGAACTCCGGCTGCAGCCGCCAGCACCCGAAACGCGCCCGGGACCCACGTGGTT CTGCTTAGGTTTGAACTCCGGCTGCAGCCGCCGGCACCCGAAACGCGCCCGGGACCCACGTGGTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:51153576..51153740;chr17:51153576..51153752 26863196 MeRIP-seq:(Medium) rs1465737513 Functional Loss SNV dbSNP153 33..33 33 - - - 97627 RMVar_ID_97627 Human_SNP_ID_626798500 m1A Human chr17 + 51153659 51153659 51153659 GCTGCAGCCGGAGTTCAAACCTAAGCAGCTGGAAGGGTAAGAGGTGTTCGGGATCCTGAGAGGAA GCTGCAGCCGGAGTTCAAACCTAAGCAGCTGGGAGGGTAAGAGGTGTTCGGGATCCTGAGAGGAA A G NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding 5'UTR,5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:51153601..51153675 32194978 MeRIP-seq:(Medium) rs1233549113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766293,Human_RBP_ID_819238,Human_RBP_ID_1537249,Human_RBP_ID_4465540,Human_RBP_ID_5114764,Human_RBP_ID_5143293,Human_RBP_ID_5318480,Human_RBP_ID_5467568,Human_RBP_ID_8941907,Human_RBP_ID_9327366,Human_RBP_ID_17654820,Human_RBP_ID_22445606,Human_RBP_ID_26812583 Human_Splice_Rec_1842253,Human_Splice_Rec_1842261,Human_Splice_Rec_1842263,Human_Splice_Rec_1842273,Human_Splice_Rec_1842281,Human_Splice_Rec_1842287,Human_Splice_Rec_1842293,Human_Splice_Rec_1842301,Human_Splice_Rec_1842315,Human_Splice_Rec_1842329,Human_Splice_Rec_1842341 RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440 97628 RMVar_ID_97628 Human_SNP_ID_626798630 m1A Human chr17 - 51154215 51154215 51154215 TCTATGGTACCTAGCCACAGGGCCTAGCAGTCAATAGGAGCAAAGAAAATCATTTATCACCATTC TCTATGGTACCTAGCCACAGGGCCTAGCAGTCGATAGGAGCAAAGAAAATCATTTATCACCATTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:51154212..51154355 26863196 MeRIP-seq:(Medium) rs911502742 Functional Loss SNV dbSNP153 33..33 33 - - - 97629 RMVar_ID_97629 Human_SNP_ID_626798631 m1A Human chr17 - 51154215 51154215 51154215 TCTATGGTACCTAGCCACAGGGCCTAGCAGTCAATAGGAGCAAAGAAAATCATTTATCACCATTC TCTATGGTACCTAGCCACAGGGCCTAGCAGTCCATAGGAGCAAAGAAAATCATTTATCACCATTC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:51154212..51154355 26863196 MeRIP-seq:(Medium) rs911502742 Functional Loss SNV dbSNP153 33..33 33 - - - 97630 RMVar_ID_97630 Human_SNP_ID_626798990 m1A Human chr17 + 51155593 51155593 51155593 ACCAGCTTTATGGGATAATCCGCTTGAGACGGATGACGCTGTAGGCAAGTGATTCACTGCTGTTT ACCAGCTTTATGGGATAATCCGCTTGAGACGGTTGACGCTGTAGGCAAGTGATTCACTGCTGTTT A T NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:51155589..51160003 26863410 MeRIP-seq:(Medium) rs1434604773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13071665 RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778 97631 RMVar_ID_97631 Human_SNP_ID_626798992 m1A Human chr17 - 51155600 51155600 51155600 AGGAATGAAACAGCAGTGAATCACTTGCCTACAGCGTCATCCGTCTCAAGCGGATTATCCCATAA AGGAATGAAACAGCAGTGAATCACTTGCCTACGGCGTCATCCGTCTCAAGCGGATTATCCCATAA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:51155597..51155723 26863196 MeRIP-seq:(Medium) rs1318793261 Functional Loss SNV dbSNP153 33..33 33 - - - 97632 RMVar_ID_97632 Human_SNP_ID_626798993 m1A Human chr17 - 51155600 51155600 51155600 AGGAATGAAACAGCAGTGAATCACTTGCCTACAGCGTCATCCGTCTCAAGCGGATTATCCCATAA AGGAATGAAACAGCAGTGAATCACTTGCCTACCGCGTCATCCGTCTCAAGCGGATTATCCCATAA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:51155597..51155723 26863196 MeRIP-seq:(Medium) rs1318793261 Functional Loss SNV dbSNP153 33..33 33 - - - 97633 RMVar_ID_97633 Human_SNP_ID_626799020 m1A Human chr17 - 51155696 51155696 51155696 ATAATCTCTCCCACAAGACCCCGCTGGACCCCATCTGGTTTGATCGCAATGAAGGTACGCTCACA ATAATCTCTCCCACAAGACCCCGCTGGACCCCGTCTGGTTTGATCGCAATGAAGGTACGCTCACA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:51155574..51155750 26863196 MeRIP-seq:(Medium) rs1412716113 Functional Loss SNV dbSNP153 33..33 33 - - - 97634 RMVar_ID_97634 Human_SNP_ID_626799034 m1A Human chr17 + 51155722 51155722 51155722 ACCAGATGGGGTCCAGCGGGGTCTTGTGGGAGAGATTATCAAGCGTTTTGAGCAGAAAGGATTCC ACCAGATGGGGTCCAGCGGGGTCTTGTGGGAGGGATTATCAAGCGTTTTGAGCAGAAAGGATTCC A G NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51154218..51155800 26863196 MeRIP-seq:(Medium) rs1282562184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46766,Human_RBP_ID_235562,Human_RBP_ID_764286,Human_RBP_ID_1182920,Human_RBP_ID_1537258,Human_RBP_ID_1862717,Human_RBP_ID_3528310,Human_RBP_ID_4438770,Human_RBP_ID_5115569,Human_RBP_ID_5467569,Human_RBP_ID_6613104,Human_RBP_ID_8456845,Human_RBP_ID_8941838,Human_RBP_ID_13071667,Human_RBP_ID_17654821,Human_RBP_ID_17904420,Human_RBP_ID_18190909,Human_RBP_ID_20291970,Human_RBP_ID_22443791,Human_RBP_ID_22807930,Human_RBP_ID_23129432,Human_RBP_ID_23734911,Human_RBP_ID_26812586,Human_RBP_ID_26966249,Human_RBP_ID_27666767 Human_Splice_Rec_1842254,Human_Splice_Rec_1842255,Human_Splice_Rec_1842262,Human_Splice_Rec_1842266,Human_Splice_Rec_1842267,Human_Splice_Rec_1842276,Human_Splice_Rec_1842277,Human_Splice_Rec_1842284,Human_Splice_Rec_1842285,Human_Splice_Rec_1842288,Human_Splice_Rec_1842289,Human_Splice_Rec_1842294,Human_Splice_Rec_1842295,Human_Splice_Rec_1842304,Human_Splice_Rec_1842305,Human_Splice_Rec_1842312,Human_Splice_Rec_1842314,Human_Splice_Rec_1842316,Human_Splice_Rec_1842317,Human_Splice_Rec_1842330,Human_Splice_Rec_1842331,Human_Splice_Rec_1842344,Human_Splice_Rec_1842345 Human_miRNA_ID_1693850,Human_miRNA_ID_1693851,Human_miRNA_ID_2233431,Human_miRNA_ID_2868665 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_284166,RMVar_hsa_circ_39095,RMVar_hsa_circ_114119,RMVar_hsa_circ_185443,RMVar_hsa_circ_185444,RMVar_hsa_circ_185442 97635 RMVar_ID_97635 Human_SNP_ID_626800012 m1A Human chr17 - 51160080 51160080 51160080 TACTTGGAGTATCCCACACAGGCACACTCACCATGGCAACTACCGGCCCTGAGTGCATGTATTTC TACTTGGAGTATCCCACACAGGCACACTCACCCTGGCAACTACCGGCCCTGAGTGCATGTATTTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:51159928..51160137;chr17:51159976..51160100 26863196 MeRIP-seq:(Medium) rs887812757 Functional Loss SNV dbSNP153 33..33 33 - - - 97636 RMVar_ID_97636 Human_SNP_ID_626800348 m1A Human chr17 + 51161271 51161270 51161271 CCATCCGTGGAGACTTCTGCATACAAGTTGGCAGGTGAGATTTTGGTATTTTTCCCCCTTTTCCA CCATCCGTGGAGACTTCTGCATACAAGTTGGC_GGTGAGATTTTGGTATTTTTCCCCCTTTTCCA CA C NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51161116..51161311 26863196 MeRIP-seq:(Medium) rs1568122698 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5115210,Human_RBP_ID_22760854 Human_Splice_Rec_1842259,Human_Splice_Rec_1842271,Human_Splice_Rec_1842299,Human_Splice_Rec_1842309,Human_Splice_Rec_1842321,Human_Splice_Rec_1842335,Human_Splice_Rec_1842349 Human_miRNA_ID_1478388,Human_miRNA_ID_1478389 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_25513,RMVar_hsa_circ_39095,RMVar_hsa_circ_114119,RMVar_hsa_circ_51912,RMVar_hsa_circ_185443,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_314766,RMVar_hsa_circ_185445 97637 RMVar_ID_97637 Human_SNP_ID_626800349 m1A Human chr17 + 51161271 51161271 51161271 CCATCCGTGGAGACTTCTGCATACAAGTTGGCAGGTGAGATTTTGGTATTTTTCCCCCTTTTCCA CCATCCGTGGAGACTTCTGCATACAAGTTGGCGGGTGAGATTTTGGTATTTTTCCCCCTTTTCCA A G NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51161116..51161311 26863196 MeRIP-seq:(Medium) rs763630436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115210,Human_RBP_ID_22760854 Human_Splice_Rec_1842259,Human_Splice_Rec_1842271,Human_Splice_Rec_1842299,Human_Splice_Rec_1842309,Human_Splice_Rec_1842321,Human_Splice_Rec_1842335,Human_Splice_Rec_1842349 Human_miRNA_ID_1478388,Human_miRNA_ID_1478389 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_25513,RMVar_hsa_circ_39095,RMVar_hsa_circ_114119,RMVar_hsa_circ_51912,RMVar_hsa_circ_185443,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_314766,RMVar_hsa_circ_185445 97638 RMVar_ID_97638 Human_SNP_ID_626800432 m1A Human chr17 - 51161685 51161685 51161685 AAAGAGATAGTCACATGACCAAGACCAGAAGGATTAAAATGCGCCCATTGCCAGAAATCTACAGC AAAGAGATAGTCACATGACCAAGACCAGAAGGTTTAAAATGCGCCCATTGCCAGAAATCTACAGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51161683..51161968 26863196 MeRIP-seq:(Medium) rs746860640 Functional Loss SNV dbSNP153 33..33 33 - - - 97639 RMVar_ID_97639 Human_SNP_ID_626801645 m1A Human chr17 - 51166451 51166451 51166451 GGCCGGGCGGCGGCGCTGCGCTGGGAGAGCAGAGAGCTGGTGCGACCACCACACCCGGGAGCCGG GGCCGGGCGGCGGCGCTGCGCTGGGAGAGCAGTGAGCTGGTGCGACCACCACACCCGGGAGCCGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:51166401..51166608 26863196 MeRIP-seq:(Medium) rs1568125284 Functional Loss SNV dbSNP153 33..33 33 - - - 97640 RMVar_ID_97640 Human_SNP_ID_626801646 m1A Human chr17 + 51166467 51166467 51166467 GTGGTCGCACCAGCTCTCTGCTCTCCCAGCGCAGCGCCGCCGCCCGGCCCCTCCAGCTTCCCGGT GTGGTCGCACCAGCTCTCTGCTCTCCCAGCGCTGCGCCGCCGCCCGGCCCCTCCAGCTTCCCGGT A T NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:51166401..51166603;chr17:51166401..51166608;chr17:51161126..51166983;chr17:51166387..51170093;chr17:51160051..51167006;chr17:51166376..51166592 26863196 MeRIP-seq:(Medium) rs994090151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46769,Human_RBP_ID_235408,Human_RBP_ID_493747,Human_RBP_ID_764291,Human_RBP_ID_903550,Human_RBP_ID_4438815,Human_RBP_ID_5441640,Human_RBP_ID_8253528,Human_RBP_ID_17260745,Human_RBP_ID_17492309,Human_RBP_ID_18190910,Human_RBP_ID_18702452,Human_RBP_ID_22532909,Human_RBP_ID_26812588 Human_Splice_Rec_1842373,Human_Splice_Rec_1842381,Human_Splice_Rec_1842389,Human_Splice_Rec_1842395 Human_miRNA_ID_2391033,Human_miRNA_ID_2592278 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_25513,RMVar_hsa_circ_114119,RMVar_hsa_circ_51912,RMVar_hsa_circ_185443,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_314766,RMVar_hsa_circ_78283,RMVar_hsa_circ_185445,RMVar_hsa_circ_185446 97641 RMVar_ID_97641 Human_SNP_ID_626801647 m1A Human chr17 - 51166493 51166470 51166494 GCCAGGGGATGCGCCCCCACCGCCTTACCGGGAAGCTGGAGGGGCCGGGCGGCGGCGCTGCGCTG GCCAGGGGATGCGCCCCCACCGCCTTACCGG________________________CGCTGCGCTG GCCGCCGCCCGGCCCCTCCAGCTTC G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T cell line,total RNA;HEK293T,H2O2 treatment chr17:51166401..51166592;chr17:51166401..51166537 26863196,26863410 MeRIP-seq:(Medium) rs1372790948 Functional Loss DEL dbSNP153 32..55 33 - - - 97642 RMVar_ID_97642 Human_SNP_ID_626802598 m1A Human chr17 + 51169837 51169837 51169837 TCTGCTGGGGTTAGCTGATAATCATGTCACTGATCGGTCTCATTGATGTGTCGTGTCAGGTAGGA TCTGCTGGGGTTAGCTGATAATCATGTCACTGGTCGGTCTCATTGATGTGTCGTGTCAGGTAGGA A G NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:51169834..51170000 26863196 MeRIP-seq:(Medium) rs1359674912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13072060 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_25513,RMVar_hsa_circ_51912,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_96040,RMVar_hsa_circ_78283,RMVar_hsa_circ_185445,RMVar_hsa_circ_185446,RMVar_hsa_circ_346049,RMVar_hsa_circ_185447,RMVar_hsa_circ_185449,RMVar_hsa_circ_331423,RMVar_hsa_circ_93389 97643 RMVar_ID_97643 Human_SNP_ID_626802640 m1A Human chr17 - 51169980 51169980 51169980 CTGGCTTTGAATCTGCTGGATTGGTCTCCCCAAGCATCACTCGGCCTGTCTTCACCACGTTCAGC CTGGCTTTGAATCTGCTGGATTGGTCTCCCCAGGCATCACTCGGCCTGTCTTCACCACGTTCAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:51168179..51170086 26863196 MeRIP-seq:(Medium) rs780883217 Functional Loss SNV dbSNP153 33..33 33 - - - 97644 RMVar_ID_97644 Human_SNP_ID_626803021 m1A Human chr17 + 51171434 51171434 51171434 GTCTGGAGTGCTGTCCATTGCGGTACCCATTAAACAGACTTTTGCACTTTAAAACATGGCAACTT GTCTGGAGTGCTGTCCATTGCGGTACCCATTAGACAGACTTTTGCACTTTAAAACATGGCAACTT A G NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51171431..51171683 26863196 MeRIP-seq:(Medium) rs1349618538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119324,RMVar_hsa_circ_110250,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_96040,RMVar_hsa_circ_78283,RMVar_hsa_circ_185445,RMVar_hsa_circ_185446,RMVar_hsa_circ_185447,RMVar_hsa_circ_185449,RMVar_hsa_circ_93389,RMVar_hsa_circ_96277,RMVar_hsa_circ_185451 97645 RMVar_ID_97645 Human_SNP_ID_626803081 m1A Human chr17 + 51171600 51171600 51171600 CTACAAGTCTTGTGCTCATGACTGGGTCTATGAATAAGAGGTGGACACAACAGCAGTCTCCTTCA CTACAAGTCTTGTGCTCATGACTGGGTCTATGCATAAGAGGTGGACACAACAGCAGTCTCCTTCA A C NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51171550..51171651 26863196 MeRIP-seq:(Medium) rs1362983652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46772,Human_RBP_ID_493767,Human_RBP_ID_764299,Human_RBP_ID_1009194,Human_RBP_ID_1182932,Human_RBP_ID_1537300,Human_RBP_ID_1862762,Human_RBP_ID_3528338,Human_RBP_ID_4475924,Human_RBP_ID_8456896,Human_RBP_ID_13072080,Human_RBP_ID_17376455,Human_RBP_ID_17654277,Human_RBP_ID_17895958,Human_RBP_ID_18293904,Human_RBP_ID_18702470,Human_RBP_ID_23210043,Human_RBP_ID_23734976,Human_RBP_ID_26453240,Human_RBP_ID_26812606,Human_RBP_ID_26966280,Human_RBP_ID_27256855,Human_RBP_ID_27454537 Human_miRNA_ID_1135940,Human_miRNA_ID_1135941,Human_miRNA_ID_1138454,Human_miRNA_ID_1138455,Human_miRNA_ID_2534947,Human_miRNA_ID_2534948,Human_miRNA_ID_2534949,Human_miRNA_ID_2536679,Human_miRNA_ID_2536680,Human_miRNA_ID_2536681,Human_miRNA_ID_2930354,Human_miRNA_ID_2930355,Human_miRNA_ID_2930356 RMVar_hsa_circ_119324,RMVar_hsa_circ_110250,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_96040,RMVar_hsa_circ_78283,RMVar_hsa_circ_185445,RMVar_hsa_circ_185446,RMVar_hsa_circ_185447,RMVar_hsa_circ_185449,RMVar_hsa_circ_93389,RMVar_hsa_circ_96277,RMVar_hsa_circ_185451 97646 RMVar_ID_97646 Human_SNP_ID_626826623 m1A Human chr17 - 51259908 51259908 51259908 CCCGGGGAGAGGCACCTGCCCCCAGCCCGGGGAGGGGGCGCCGCGGGCTCGGGGAGCACGGACAA CCCGGGGAGAGGCACCTGCCCCCAGCCCGGGGGGGGGGCGCCGCGGGCTCGGGGAGCACGGACAA T C MBTD1 Ensembl:ENSG00000011258 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:51259884..51260025 26863196 MeRIP-seq:(Medium) rs957913139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235580,Human_RBP_ID_262323,Human_RBP_ID_819262,Human_RBP_ID_4466610,Human_RBP_ID_22217438,Human_RBP_ID_22716579 Human_Splice_Rec_1842409,Human_Splice_Rec_1842469 RMVar_hsa_circ_185471,RMVar_hsa_circ_77547 97647 RMVar_ID_97647 Human_SNP_ID_626826634 m1A Human chr17 - 51259927 51259927 51259927 CCCCTGTAGTCGCCGCAGTCCCGGGGAGAGGCACCTGCCCCCAGCCCGGGGAGGGGGCGCCGCGG CCCCTGTAGTCGCCGCAGTCCCGGGGAGAGGCGCCTGCCCCCAGCCCGGGGAGGGGGCGCCGCGG T C MBTD1 Ensembl:ENSG00000011258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51259876..51260002 26863196 MeRIP-seq:(Medium) rs1037317624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235580,Human_RBP_ID_4466610 Human_Splice_Rec_1842409,Human_Splice_Rec_1842469 RMVar_hsa_circ_185471,RMVar_hsa_circ_77547 97648 RMVar_ID_97648 Human_SNP_ID_626826984 m1A Human chr17 + 51260612 51260612 51260612 TAACGATGCCGCCGGAGCGGAGGAGACGAATGAAACTGGACCGGAGAACCGGAGCGAAGCCGAAG TAACGATGCCGCCGGAGCGGAGGAGACGAATGGAACTGGACCGGAGAACCGGAGCGAAGCCGAAG A G UTP18 Ensembl:ENSG00000011260 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:51260526..51266225 26863196 MeRIP-seq:(Medium) rs1274343659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819263,Human_RBP_ID_3528461,Human_RBP_ID_4439026,Human_RBP_ID_5577558,Human_RBP_ID_9289242,Human_RBP_ID_9376395,Human_RBP_ID_13073821,Human_RBP_ID_22445613,Human_RBP_ID_22954179,Human_RBP_ID_26330806,Human_RBP_ID_27812917 Human_miRNA_ID_2071327,Human_miRNA_ID_2804252 RMVar_hsa_circ_98835,RMVar_hsa_circ_185473 97649 RMVar_ID_97649 Human_SNP_ID_626826993 m1A Human chr17 + 51260619 51260619 51260619 GCCGCCGGAGCGGAGGAGACGAATGAAACTGGACCGGAGAACCGGAGCGAAGCCGAAGCGGAAGC GCCGCCGGAGCGGAGGAGACGAATGAAACTGGGCCGGAGAACCGGAGCGAAGCCGAAGCGGAAGC A G UTP18 Ensembl:ENSG00000011260 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:51260526..51260959 26863196 MeRIP-seq:(Medium) rs1324950275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819263,Human_RBP_ID_3528461,Human_RBP_ID_4465547,Human_RBP_ID_5577558,Human_RBP_ID_9289242,Human_RBP_ID_9376395,Human_RBP_ID_13073821,Human_RBP_ID_22445613,Human_RBP_ID_22954179,Human_RBP_ID_26330806,Human_RBP_ID_27812917 Human_miRNA_ID_2071327,Human_miRNA_ID_2804252,Human_miRNA_ID_3002806 RMVar_hsa_circ_98835,RMVar_hsa_circ_185473 97650 RMVar_ID_97650 Human_SNP_ID_626827019 m1A Human chr17 + 51260637 51260637 51260637 ACGAATGAAACTGGACCGGAGAACCGGAGCGAAGCCGAAGCGGAAGCCCGGAATGAGGCCGGACT ACGAATGAAACTGGACCGGAGAACCGGAGCGAGGCCGAAGCGGAAGCCCGGAATGAGGCCGGACT A G UTP18 Ensembl:ENSG00000011260 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51260514..51266214 26863196 MeRIP-seq:(Medium) rs367594840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764301,Human_RBP_ID_3528461,Human_RBP_ID_4465547,Human_RBP_ID_9289242,Human_RBP_ID_9376395,Human_RBP_ID_22445613,Human_RBP_ID_26330806,Human_RBP_ID_27812917 RMVar_hsa_circ_98835,RMVar_hsa_circ_185473 97651 RMVar_ID_97651 Human_SNP_ID_626827501 m1A Human chr17 + 51261630 51261630 51261630 TCCCTGCCTTTTGGCGCTTGTGTGCTAGTGGCAGAGACAAGATAGAGGAGATAAACGAGTAAACT TCCCTGCCTTTTGGCGCTTGTGTGCTAGTGGCGGAGACAAGATAGAGGAGATAAACGAGTAAACT A G UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:51261626..51261777 26863196 MeRIP-seq:(Medium) rs1328826559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98835,RMVar_hsa_circ_185473 97652 RMVar_ID_97652 Human_SNP_ID_626828033 m1A Human chr17 + 51263336 51263336 51263336 GAAGTGGAGAATGAAGCAAAAGGTAATTTTCCACCTCAAAAGAAGCCAGTTTGGGTGGATGAAGA GAAGTGGAGAATGAAGCAAAAGGTAATTTTCCCCCTCAAAAGAAGCCAGTTTGGGTGGATGAAGA A C UTP18 Ensembl:ENSG00000011260 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:51263228..51263400 26863196 MeRIP-seq:(Medium) rs747087948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46777,Human_RBP_ID_4439052,Human_RBP_ID_20291972,Human_RBP_ID_23735117,Human_RBP_ID_26966334,Human_RBP_ID_27812920 Human_Splice_Rec_1842546,Human_Splice_Rec_1842547 RMVar_hsa_circ_185475,RMVar_hsa_circ_110010,RMVar_hsa_circ_293535,RMVar_hsa_circ_98835,RMVar_hsa_circ_369667,RMVar_hsa_circ_185473,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_283940,RMVar_hsa_circ_270997,RMVar_hsa_circ_185477,RMVar_hsa_circ_185479,RMVar_hsa_circ_185480,RMVar_hsa_circ_185478,RMVar_hsa_circ_185476,RMVar_hsa_circ_185474 97653 RMVar_ID_97653 Human_SNP_ID_626833609 m1A Human chr17 + 51282511 51282491 51282511 GGAAGGGAGGGAGGGAAGGAAGGAAAGATGGAAGGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GGAAGGGAGGGAG____________________GGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GGGAAGGAAGGAAAGATGGAA G UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51282461..51282625 26863196 MeRIP-seq:(Medium) rs922743968 Functional Loss DEL dbSNP153 14..33 33 - - - RMVar_hsa_circ_25562,RMVar_hsa_circ_185475,RMVar_hsa_circ_369667,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_185476,RMVar_hsa_circ_125773,RMVar_hsa_circ_185474,RMVar_hsa_circ_272858,RMVar_hsa_circ_185484,RMVar_hsa_circ_365891,RMVar_hsa_circ_120638,RMVar_hsa_circ_185486,RMVar_hsa_circ_334960,RMVar_hsa_circ_185485,RMVar_hsa_circ_333354,RMVar_hsa_circ_57920,RMVar_hsa_circ_185488,RMVar_hsa_circ_185489,RMVar_hsa_circ_123397,RMVar_hsa_circ_86134,RMVar_hsa_circ_346876,RMVar_hsa_circ_185490 97654 RMVar_ID_97654 Human_SNP_ID_626833617 m1A Human chr17 + 51282511 51282509 51282511 GGAAGGGAGGGAGGGAAGGAAGGAAAGATGGAAGGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GGAAGGGAGGGAGGGAAGGAAGGAAAGATGG__GGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GAA G UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51282461..51282625 26863196 MeRIP-seq:(Medium) rs1258605801 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_25562,RMVar_hsa_circ_185475,RMVar_hsa_circ_369667,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_185476,RMVar_hsa_circ_125773,RMVar_hsa_circ_185474,RMVar_hsa_circ_272858,RMVar_hsa_circ_185484,RMVar_hsa_circ_365891,RMVar_hsa_circ_120638,RMVar_hsa_circ_185486,RMVar_hsa_circ_334960,RMVar_hsa_circ_185485,RMVar_hsa_circ_333354,RMVar_hsa_circ_57920,RMVar_hsa_circ_185488,RMVar_hsa_circ_185489,RMVar_hsa_circ_123397,RMVar_hsa_circ_86134,RMVar_hsa_circ_346876,RMVar_hsa_circ_185490 97655 RMVar_ID_97655 Human_SNP_ID_626833618 m1A Human chr17 + 51282511 51282511 51282511 GGAAGGGAGGGAGGGAAGGAAGGAAAGATGGAAGGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GGAAGGGAGGGAGGGAAGGAAGGAAAGATGGATGGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA A T UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51282461..51282625 26863196 MeRIP-seq:(Medium) rs113666317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25562,RMVar_hsa_circ_185475,RMVar_hsa_circ_369667,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_185476,RMVar_hsa_circ_125773,RMVar_hsa_circ_185474,RMVar_hsa_circ_272858,RMVar_hsa_circ_185484,RMVar_hsa_circ_365891,RMVar_hsa_circ_120638,RMVar_hsa_circ_185486,RMVar_hsa_circ_334960,RMVar_hsa_circ_185485,RMVar_hsa_circ_333354,RMVar_hsa_circ_57920,RMVar_hsa_circ_185488,RMVar_hsa_circ_185489,RMVar_hsa_circ_123397,RMVar_hsa_circ_86134,RMVar_hsa_circ_346876,RMVar_hsa_circ_185490 97656 RMVar_ID_97656 Human_SNP_ID_626835098 m1A Human chr17 + 51287661 51287661 51287661 GTGCATAATTAGGACTAAAGGCACTGATTTGGATGTGGTGGGTGATAGGTGGTCTGTGGGAGTAA GTGCATAATTAGGACTAAAGGCACTGATTTGGTTGTGGTGGGTGATAGGTGGTCTGTGGGAGTAA A T UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51287638..51287761 26863196 MeRIP-seq:(Medium) rs1269431699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23735162 RMVar_hsa_circ_25562,RMVar_hsa_circ_185475,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_125773,RMVar_hsa_circ_185474,RMVar_hsa_circ_272858,RMVar_hsa_circ_185484,RMVar_hsa_circ_365891,RMVar_hsa_circ_334960,RMVar_hsa_circ_185485,RMVar_hsa_circ_333354,RMVar_hsa_circ_57920,RMVar_hsa_circ_185488,RMVar_hsa_circ_185489,RMVar_hsa_circ_123397,RMVar_hsa_circ_346876,RMVar_hsa_circ_324667,RMVar_hsa_circ_88985,RMVar_hsa_circ_23236,RMVar_hsa_circ_185491 97657 RMVar_ID_97657 Human_SNP_ID_627281480 m1A Human chr17 - 53106344 53106343 53106344 ATTCCTTCCTTTTTTGTCTAGATTTTATGTATACGGGTTCTTCGAATGTGTGGTAGGGTGGGGCG ATTCCTTCCTTTTTTGTCTAGATTTTATGTAT_CGGGTTCTTCGAATGTGTGGTAGGGTGGGGCG GT G KP702293-001 RNACentral:URS00008268E8 tRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:53106306..53106396 26863410 MeRIP-seq:(Medium) rs1183815702 Functional Loss DEL dbSNP153 33..33 33 - - - 97658 RMVar_ID_97658 Human_SNP_ID_627720216 m1A Human chr17 - 54900862 54900862 54900862 GGATCCCGGTGACTCTTGCCAAACGCCATGGTAGCGCCAGAGGGCCGGGCCCAGGAAATCCGCCT GGATCCCGGTGACTCTTGCCAAACGCCATGGTGGCGCCAGAGGGCCGGGCCCAGGAAATCCGCCT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:54900799..54900912 26863196 MeRIP-seq:(Medium) rs754345519 Functional Loss SNV dbSNP153 33..33 33 - - - 97659 RMVar_ID_97659 Human_SNP_ID_627720231 m1A Human chr17 - 54900892 54900892 54900892 CCTATGAGGTGGCCCACGGAGGTCGCGTAGGGATCCCGGTGACTCTTGCCAAACGCCATGGTAGC CCTATGAGGTGGCCCACGGAGGTCGCGTAGGGGTCCCGGTGACTCTTGCCAAACGCCATGGTAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:54900734..54900910 26863196 MeRIP-seq:(Medium) rs1238735911 Functional Loss SNV dbSNP153 33..33 33 - - - 97660 RMVar_ID_97660 Human_SNP_ID_627720239 m1A Human chr17 + 54900915 54900915 54900915 TCACCGGGATCCCTACGCGACCTCCGTGGGCCACCTCATAGGTAAGGAGGCGCGGGGAGAGACGC TCACCGGGATCCCTACGCGACCTCCGTGGGCCCCCTCATAGGTAAGGAGGCGCGGGGAGAGACGC A C TOM1L1 Ensembl:ENSG00000141198 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:54900772..54900936 26863196 MeRIP-seq:(Medium) rs760817454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465548,Human_RBP_ID_9378582,Human_RBP_ID_19079535 Human_Splice_Rec_1842841,Human_Splice_Rec_1842861,Human_Splice_Rec_1842875,Human_Splice_Rec_1842905,Human_Splice_Rec_1842933,Human_Splice_Rec_1842945,Human_Splice_Rec_1842965,Human_Splice_Rec_1842995,Human_Splice_Rec_1843025,Human_Splice_Rec_1843037,Human_Splice_Rec_1843063,Human_Splice_Rec_1843089,Human_Splice_Rec_1843107,Human_Splice_Rec_1843119,Human_Splice_Rec_1843129 97661 RMVar_ID_97661 Human_SNP_ID_627735271 m1A Human chr17 - 54964775 54964775 54964775 AAGATTGAAAACATGGTGCCTGTTAAAGATCGAATCATTAAAATTAGCTTTAATGCAGATGTGCA AAGATTGAAAACATGGTGCCTGTTAAAGATCGGATCATTAAAATTAGCTTTAATGCAGATGTGCA T C COX11 Ensembl:ENSG00000166260 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:54964726..54964800 32194978 MeRIP-seq:(Medium) rs376915335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1863262,Human_RBP_ID_13079162,Human_RBP_ID_18702861,Human_RBP_ID_22954297,Human_RBP_ID_23735671 Human_Splice_Rec_1843192,Human_Splice_Rec_1843193,Human_Splice_Rec_1843206,Human_Splice_Rec_1843207,Human_Splice_Rec_1843220,Human_Splice_Rec_1843221,Human_Splice_Rec_1843226,Human_Splice_Rec_1843227 97662 RMVar_ID_97662 Human_SNP_ID_627841233 m1A Human chr17 - 55421928 55421928 55421928 GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGAGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGTGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:55421826..55421950 26863410 MeRIP-seq:(Medium) rs912124451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2016945 RMVar_hsa_circ_185533,RMVar_hsa_circ_75941 97663 RMVar_ID_97663 Human_SNP_ID_627841234 m1A Human chr17 - 55421928 55421928 55421928 GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGAGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGGGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:55421826..55421950 26863410 MeRIP-seq:(Medium) rs912124451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2016945 RMVar_hsa_circ_185533,RMVar_hsa_circ_75941 97664 RMVar_ID_97664 Human_SNP_ID_627841235 m1A Human chr17 - 55421928 55421928 55421928 GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGAGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT GGGGCGGAGGAGCCGGGGAGGCGGGAGGCGGGCGGCGGGAGGTGTTGGGGCCGTTGAAGCGGCCT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:55421826..55421950 26863410 MeRIP-seq:(Medium) rs912124451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2016945 RMVar_hsa_circ_185533,RMVar_hsa_circ_75941 97665 RMVar_ID_97665 Human_SNP_ID_627923601 m1A Human chr17 + 55751165 55751165 55751165 GGAGCAGTTCTGGGAGGCCTGCGCCGAGCTCCAGCAGCCCGCTCTGGCCGGGGCCGACTGGCAGC GGAGCAGTTCTGGGAGGCCTGCGCCGAGCTCCGGCAGCCCGCTCTGGCCGGGGCCGACTGGCAGC A G PCTP Ensembl:ENSG00000141179 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:55751115..55751180 26863196 MeRIP-seq:(Medium) rs1259764984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897731,Human_RBP_ID_4464679,Human_RBP_ID_9376414,Human_RBP_ID_18420599,Human_RBP_ID_18991831,Human_RBP_ID_22444781,Human_RBP_ID_22959864,Human_RBP_ID_23118919 Human_Splice_Rec_1843487,Human_Splice_Rec_1843497,Human_Splice_Rec_1843507 97666 RMVar_ID_97666 Human_SNP_ID_628123393 m1A Human chr17 - 56592768 56592768 56592768 CACCATCCTCCTCCTCCTTGGCCGGGTCCTGCACCCTGAGTGGCCTAGCCTCAGGGGCGCGACTG CACCATCCTCCTCCTCCTTGGCCGGGTCCTGCGCCCTGAGTGGCCTAGCCTCAGGGGCGCGACTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56592717..56592845 26863196 MeRIP-seq:(Medium) rs915050280 Functional Loss SNV dbSNP153 33..33 33 - - - 97667 RMVar_ID_97667 Human_SNP_ID_628123645 m1A Human chr17 - 56593389 56593365 56593389 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGC________________________GCTTGGCAG CGCCACCGCCGCCGCCACCGCCGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs1449635356 Functional Loss DEL dbSNP153 33..56 33 - - - 97668 RMVar_ID_97668 Human_SNP_ID_628123646 m1A Human chr17 - 56593389 56593369 56593390 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGG_____________________TGGCGCTTGGCAG ACCGCCGCCGCCACCGCCGCTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs1023221014 Functional Loss DEL dbSNP153 32..52 33 - - - 97669 RMVar_ID_97669 Human_SNP_ID_628123653 m1A Human chr17 - 56593389 56593371 56593389 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGC__________________GGTGGCGCTTGGCAG CGCCGCCGCCACCGCCGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs888662681 Functional Loss DEL dbSNP153 33..50 33 - - - 97670 RMVar_ID_97670 Human_SNP_ID_628123660 m1A Human chr17 - 56593389 56593377 56593389 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGC____________GGCGGCGGTGGCGCTTGGCAG CGCCACCGCCGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs1418089494 Functional Loss DEL dbSNP153 33..44 33 - - - 97671 RMVar_ID_97671 Human_SNP_ID_628123665 m1A Human chr17 - 56593389 56593381 56593390 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGG_________TGGCGGCGGCGGTGGCGCTTGGCAG ACCGCCGCTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs889486145 Functional Loss DEL dbSNP153 32..40 33 - - - 97672 RMVar_ID_97672 Human_SNP_ID_628123671 m1A Human chr17 - 56593389 56593389 56593389 CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCAGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG CGGAGCTCACAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGTGGCGCTTGGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56593358..56593522 26863196 MeRIP-seq:(Medium) rs1218883498 Functional Loss SNV dbSNP153 33..33 33 - - - 97673 RMVar_ID_97673 Human_SNP_ID_628123797 m1A Human chr17 - 56593743 56593734 56593743 GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCCAGCGGCGGCGGCGGCGGCGGCGTCCGCGCACGT GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCC_________GGCGGCGGCGGCGTCCGCGCACGT CGCCGCCGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56593642..56594171 26863196 MeRIP-seq:(Medium) rs1325237244 Functional Loss DEL dbSNP153 33..41 33 - - - 97674 RMVar_ID_97674 Human_SNP_ID_628123802 m1A Human chr17 - 56593743 56593740 56593743 GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCCAGCGGCGGCGGCGGCGGCGGCGTCCGCGCACGT GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCC___GGCGGCGGCGGCGGCGGCGTCCGCGCACGT CGCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56593642..56594171 26863196 MeRIP-seq:(Medium) rs985609154 Functional Loss DEL dbSNP153 33..35 33 - - - 97675 RMVar_ID_97675 Human_SNP_ID_628123805 m1A Human chr17 - 56593743 56593743 56593743 GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCCAGCGGCGGCGGCGGCGGCGGCGTCCGCGCACGT GGCTCCGCGGCCGGCTCTGCCCGGCGGACTCCGGCGGCGGCGGCGGCGGCGGCGTCCGCGCACGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56593642..56594171 26863196 MeRIP-seq:(Medium) rs926848482 Functional Loss SNV dbSNP153 33..33 33 - - - 97676 RMVar_ID_97676 Human_SNP_ID_628124153 m1A Human chr17 + 56594552 56594552 56594552 GGACCTGGCGGAGCTGGACCAGCTGCTGCGGCAGCGGCCGTCGGGGGCCATGCCGAGCGAGATCA GGACCTGGCGGAGCTGGACCAGCTGCTGCGGCCGCGGCCGTCGGGGGCCATGCCGAGCGAGATCA A C NOG Ensembl:ENSG00000183691 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56594504..56594592 26863196 MeRIP-seq:(Medium) rs868405669 Functional Loss SNV dbSNP153 33..33 33 - - - 97677 RMVar_ID_97677 Human_SNP_ID_628177939 m1A Human chr17 - 56809880 56809878 56809880 GTGTAAGGGTGTGTGTAAGGGGTGTGTGTGAGAGGTGTGTGAAGGTGCAGGTGTGTGTGAGGGTG GTGTAAGGGTGTGTGTAAGGGGTGTGTGTGAG__GTGTGTGAAGGTGCAGGTGTGTGTGAGGGTG CCT C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56809834..56809928 26863196 MeRIP-seq:(Medium) rs1205084966 Functional Loss DEL dbSNP153 33..34 33 - - - 97678 RMVar_ID_97678 Human_SNP_ID_628177941 m1A Human chr17 - 56809880 56809880 56809880 GTGTAAGGGTGTGTGTAAGGGGTGTGTGTGAGAGGTGTGTGAAGGTGCAGGTGTGTGTGAGGGTG GTGTAAGGGTGTGTGTAAGGGGTGTGTGTGAGGGGTGTGTGAAGGTGCAGGTGTGTGTGAGGGTG T C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56809834..56809928 26863196 MeRIP-seq:(Medium) rs1392173806 Functional Loss SNV dbSNP153 33..33 33 - - - 97679 RMVar_ID_97679 Human_SNP_ID_628177947 m1A Human chr17 + 56809890 56809890 56809890 CACACCTGCACCTTCACACACCTCTCACACACACCCCTTACACACACCCTTACACACACCCTCAC CACACCTGCACCTTCACACACCTCTCACACACGCCCCTTACACACACCCTTACACACACCCTCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56809852..56809951 26863196 MeRIP-seq:(Medium) rs1474633691 Functional Loss SNV dbSNP153 33..33 33 - - - 97680 RMVar_ID_97680 Human_SNP_ID_628177992 m1A Human chr17 + 56809967 56809965 56809967 CATACTCCTCACACATACTCCTCACTCACCTCACACACAATCCTTGCACAGACCCTTCACACACA CATACTCCTCACACATACTCCTCACTCACCT__CACACAATCCTTGCACAGACCCTTCACACACA TCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:56809804..56810095 26863196 MeRIP-seq:(Medium) rs1175907858 Functional Loss DEL dbSNP153 32..33 33 - - - 97681 RMVar_ID_97681 Human_SNP_ID_628177996 m1A Human chr17 - 56809979 56809979 56809979 ATGTCTGGGGTGTGTGTGTGAAGGGTCTGTGCAAGGATTGTGTGTGAGGTGAGTGAGGAGTATGT ATGTCTGGGGTGTGTGTGTGAAGGGTCTGTGCGAGGATTGTGTGTGAGGTGAGTGAGGAGTATGT T C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:56809472..56810447 26863196 MeRIP-seq:(Medium) rs530293495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23736270 97682 RMVar_ID_97682 Human_SNP_ID_628183344 m1A Human chr17 - 56832634 56832634 56832634 GAACTCAGTAGTCAGGAAAGTGAAACTTGTGAAGGGTGGGTCAGTGTAAGTAAGGTTAGGCGACA GAACTCAGTAGTCAGGAAAGTGAAACTTGTGATGGGTGGGTCAGTGTAAGTAAGGTTAGGCGACA T A C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:56832583..56832741 26863196 MeRIP-seq:(Medium) rs1214268135 Functional Loss SNV dbSNP153 33..33 33 - - - 97683 RMVar_ID_97683 Human_SNP_ID_628183348 m1A Human chr17 + 56832655 56832655 56832655 CTGACCCACCCTTCACAAGTTTCACTTTCCTGACTACTGAGTTCCTGCTCATCCCCTTCACATTC CTGACCCACCCTTCACAAGTTTCACTTTCCTGGCTACTGAGTTCCTGCTCATCCCCTTCACATTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56832605..56832701 26863196 MeRIP-seq:(Medium) rs1052631153 Functional Loss SNV dbSNP153 33..33 33 - - - 97684 RMVar_ID_97684 Human_SNP_ID_628183636 m1A Human chr17 - 56833507 56833507 56833507 CGAGCGGGGCAGCCGCCCGCTCGTCGCCGCTGACCCCGAGCCCGGCCGCGGTTTCCGCCCCCTGC CGAGCGGGGCAGCCGCCCGCTCGTCGCCGCTGCCCCCGAGCCCGGCCGCGGTTTCCGCCCCCTGC T G C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:56833399..56833526 26863196 MeRIP-seq:(Medium) rs1013451939 Functional Loss SNV dbSNP153 33..33 33 - - - 97685 RMVar_ID_97685 Human_SNP_ID_628183715 m1A Human chr17 - 56833687 56833687 56833687 CGATGCCGGCGCCGCCGCCGCCGGGGATGCGTAAGCCGACTGGGAAGCGAGGGGGGGAGGCGGCC CGATGCCGGCGCCGCCGCCGCCGGGGATGCGTCAGCCGACTGGGAAGCGAGGGGGGGAGGCGGCC T G C17orf67 Ensembl:ENSG00000214226 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:56833204..56833886 26863196 MeRIP-seq:(Medium) rs1308283132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1843745 97686 RMVar_ID_97686 Human_SNP_ID_628198779 m1A Human chr17 + 56891561 56891561 56891561 CTCACCCCTTTCCTGGCTAAATCCCACCTCCCACCCTCCCGCCAGCTCCCCTCCCATGCTCCCAA CTCACCCCTTTCCTGGCTAAATCCCACCTCCCCCCCTCCCGCCAGCTCCCCTCCCATGCTCCCAA A C AC015912.1 Ensembl:ENSG00000262112 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56891513..56891620 26863196 MeRIP-seq:(Medium) rs954216087 Functional Loss SNV dbSNP153 33..33 33 - - - 97687 RMVar_ID_97687 Human_SNP_ID_628198917 m1A Human chr17 - 56891938 56891938 56891938 GCTCGGCCGCAACAGCGCCTCCTGGTGCGTGGAGTGGTTCAACACCAAGATCTCTGCCTGGCACA GCTCGGCCGCAACAGCGCCTCCTGGTGCGTGGGGTGGTTCAACACCAAGATCTCTGCCTGGCACA T C TRIM25 Ensembl:ENSG00000121060 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:56891887..56892037 32194978 MeRIP-seq:(Medium) rs1358750613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1537771,Human_RBP_ID_27454792 Human_miRNA_ID_2977739 RMVar_hsa_circ_86262,RMVar_hsa_circ_106618,RMVar_hsa_circ_122008,RMVar_hsa_circ_89768,RMVar_hsa_circ_185565,RMVar_hsa_circ_185567,RMVar_hsa_circ_78975,RMVar_hsa_circ_185568,RMVar_hsa_circ_185566,RMVar_hsa_circ_185564 97688 RMVar_ID_97688 Human_SNP_ID_628200305 m1A Human chr17 - 56897448 56897448 56897448 AAGGGGAGGAAATGGGAGAGTGAGCGACTGTGAGTGATGTGACTTCGAAGTAGGAGAAGCGGTAG AAGGGGAGGAAATGGGAGAGTGAGCGACTGTGGGTGATGTGACTTCGAAGTAGGAGAAGCGGTAG T C TRIM25 Ensembl:ENSG00000121060 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56897446..56897553 26863196 MeRIP-seq:(Medium) rs1006290580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2513715,Human_RBP_ID_9422410,Human_RBP_ID_13082725,Human_RBP_ID_22954436,Human_RBP_ID_23736422 RMVar_hsa_circ_106618,RMVar_hsa_circ_122008,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_185566,RMVar_hsa_circ_46046,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_304788,RMVar_hsa_circ_185570 97689 RMVar_ID_97689 Human_SNP_ID_628200760 m1A Human chr17 - 56899165 56899165 56899165 CTTCTTCTCTGACACAGGTGACCCTGGAGAGCATGACCCAGCGTCCACACACAAATCCACACGCC CTTCTTCTCTGACACAGGTGACCCTGGAGAGCTTGACCCAGCGTCCACACACAAATCCACACGCC T A TRIM25 Ensembl:ENSG00000121060 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:56898982..56901470 32194978 MeRIP-seq:(Medium) rs1164113253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765054,Human_RBP_ID_904379,Human_RBP_ID_9376415,Human_RBP_ID_22544531 Human_Splice_Rec_1843826,Human_Splice_Rec_1843827,Human_Splice_Rec_1843850,Human_Splice_Rec_1843851,Human_Splice_Rec_1843868,Human_Splice_Rec_1843869,Human_Splice_Rec_1843886,Human_Splice_Rec_1843887,Human_Splice_Rec_1843902,Human_Splice_Rec_1843903,Human_Splice_Rec_1843908 RMVar_hsa_circ_106618,RMVar_hsa_circ_122008,RMVar_hsa_circ_53718,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_185566,RMVar_hsa_circ_46046,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_304788,RMVar_hsa_circ_127581,RMVar_hsa_circ_185570,RMVar_hsa_circ_57800,RMVar_hsa_circ_185571 97690 RMVar_ID_97690 Human_SNP_ID_628202033 m1A Human chr17 - 56904459 56904459 56904459 CAGATGACTGCAAACAGAAAGGTGGAGCAGCTACAACAAGAATACACGGAAATGAAGGCTCTCTT CAGATGACTGCAAACAGAAAGGTGGAGCAGCTGCAACAAGAATACACGGAAATGAAGGCTCTCTT T C TRIM25 Ensembl:ENSG00000121060 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56904410..56904528 26863196 MeRIP-seq:(Medium) rs763026042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47728,Human_RBP_ID_18530773,Human_RBP_ID_26333630 Human_Splice_Rec_1843822,Human_Splice_Rec_1843846,Human_Splice_Rec_1843864,Human_Splice_Rec_1843882,Human_Splice_Rec_1843912 RMVar_hsa_circ_122008,RMVar_hsa_circ_53718,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_127581,RMVar_hsa_circ_57800,RMVar_hsa_circ_53597,RMVar_hsa_circ_185572,RMVar_hsa_circ_185571,RMVar_hsa_circ_299913,RMVar_hsa_circ_73823,RMVar_hsa_circ_366553 97691 RMVar_ID_97691 Human_SNP_ID_628202040 m1A Human chr17 - 56904476 56904476 56904476 TCTTACCTTGGCCCTCTCAGATGACTGCAAACAGAAAGGTGGAGCAGCTACAACAAGAATACACG TCTTACCTTGGCCCTCTCAGATGACTGCAAACGGAAAGGTGGAGCAGCTACAACAAGAATACACG T C TRIM25 Ensembl:ENSG00000121060 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:56904426..56904546 26863196 MeRIP-seq:(Medium) rs1194302272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47728,Human_RBP_ID_26333630 Human_Splice_Rec_1843822,Human_Splice_Rec_1843846,Human_Splice_Rec_1843864,Human_Splice_Rec_1843882,Human_Splice_Rec_1843912 RMVar_hsa_circ_122008,RMVar_hsa_circ_53718,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_127581,RMVar_hsa_circ_57800,RMVar_hsa_circ_53597,RMVar_hsa_circ_185572,RMVar_hsa_circ_185571,RMVar_hsa_circ_299913,RMVar_hsa_circ_73823,RMVar_hsa_circ_366553 97692 RMVar_ID_97692 Human_SNP_ID_628202041 m1A Human chr17 - 56904476 56904476 56904476 TCTTACCTTGGCCCTCTCAGATGACTGCAAACAGAAAGGTGGAGCAGCTACAACAAGAATACACG TCTTACCTTGGCCCTCTCAGATGACTGCAAACCGAAAGGTGGAGCAGCTACAACAAGAATACACG T G TRIM25 Ensembl:ENSG00000121060 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:56904426..56904546 26863196 MeRIP-seq:(Medium) rs1194302272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47728,Human_RBP_ID_26333630 Human_Splice_Rec_1843822,Human_Splice_Rec_1843846,Human_Splice_Rec_1843864,Human_Splice_Rec_1843882,Human_Splice_Rec_1843912 RMVar_hsa_circ_122008,RMVar_hsa_circ_53718,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_127581,RMVar_hsa_circ_57800,RMVar_hsa_circ_53597,RMVar_hsa_circ_185572,RMVar_hsa_circ_185571,RMVar_hsa_circ_299913,RMVar_hsa_circ_73823,RMVar_hsa_circ_366553 97693 RMVar_ID_97693 Human_SNP_ID_628202915 m1A Human chr17 + 56908421 56908421 56908421 GTCAGAGCCACGCCCATCCCGCGTGGAAGCTGAGCGAAGCCACAGGGCAGGGCTGGCCTTGGAGA GTCAGAGCCACGCCCATCCCGCGTGGAAGCTGGGCGAAGCCACAGGGCAGGGCTGGCCTTGGAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56908419..56908492 26863196 MeRIP-seq:(Medium) rs1348518719 Functional Loss SNV dbSNP153 33..33 33 - - - 97694 RMVar_ID_97694 Human_SNP_ID_628204164 m1A Human chr17 + 56913675 56913675 56913675 CGGCGGCCTCCTTCAGGCAGTGGTCGCAGGCCACCTGGGCATTCGGGCTGGGTGCAGAGGCGCGG CGGCGGCCTCCTTCAGGCAGTGGTCGCAGGCCTCCTGGGCATTCGGGCTGGGTGCAGAGGCGCGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:56913559..56913775 26863196 MeRIP-seq:(Medium) rs1328296875 Functional Loss SNV dbSNP153 33..33 33 - - - 97695 RMVar_ID_97695 Human_SNP_ID_628204298 m1A Human chr17 + 56913987 56913987 56913987 ACAGCTCCTCGGCCAGGGGGCACAGCTCTGCCATGGCGCTCCCAGGGGTCGGGACACAACTGCTG ACAGCTCCTCGGCCAGGGGGCACAGCTCTGCCCTGGCGCTCCCAGGGGTCGGGACACAACTGCTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56913905..56913992 26863196 MeRIP-seq:(Medium) rs570574189 Functional Loss SNV dbSNP153 33..33 33 - - - 97696 RMVar_ID_97696 Human_SNP_ID_628225881 m1A Human chr17 - 57001969 57001969 57001969 AGAGAAAGGCCTGGCATTAACAGCTGGATAGAATAGGAAAAAAGTCTAGGTCCTAAAAGTTGGTG AGAGAAAGGCCTGGCATTAACAGCTGGATAGAGTAGGAAAAAAGTCTAGGTCCTAAAAGTTGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57001966..57002079 26863196 MeRIP-seq:(Medium) rs1328568676 Functional Loss SNV dbSNP153 33..33 33 - - - 97697 RMVar_ID_97697 Human_SNP_ID_628251074 m1A Human chr17 + 57099812 57099812 57099812 TCTGAGGACTGAGAACAGGGCAGGTGAAGTGCAGGGAGCCTAGTGACAGAAGGTGCTGGGGACTG TCTGAGGACTGAGAACAGGGCAGGTGAAGTGCGGGGAGCCTAGTGACAGAAGGTGCTGGGGACTG A G AKAP1 Ensembl:ENSG00000121057 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:57099777..57099906 26863196 MeRIP-seq:(Medium) rs967430563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13083657 97698 RMVar_ID_97698 Human_SNP_ID_628251075 m1A Human chr17 + 57099812 57099812 57099812 TCTGAGGACTGAGAACAGGGCAGGTGAAGTGCAGGGAGCCTAGTGACAGAAGGTGCTGGGGACTG TCTGAGGACTGAGAACAGGGCAGGTGAAGTGCTGGGAGCCTAGTGACAGAAGGTGCTGGGGACTG A T AKAP1 Ensembl:ENSG00000121057 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:57099777..57099906 26863196 MeRIP-seq:(Medium) rs967430563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13083657 97699 RMVar_ID_97699 Human_SNP_ID_628252456 m1A Human chr17 - 57105447 57105447 57105447 GAACTGGATTGCCATCCTGGAGGCTTGAAGTAATTACACCTGGGGAGAGCAGGAGAGCGGGGAGG GAACTGGATTGCCATCCTGGAGGCTTGAAGTAGTTACACCTGGGGAGAGCAGGAGAGCGGGGAGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:57105426..57105500 26863410 MeRIP-seq:(Medium) rs1027450338 Functional Loss SNV dbSNP153 33..33 33 - - - 97700 RMVar_ID_97700 Human_SNP_ID_628252557 m1A Human chr17 + 57105734 57105734 57105734 AAGGAACTGTCCACCGTGAGCAAGCTGCCTGCAGAGCCCCCAGCATTGCTCCAGACACACCCACC AAGGAACTGTCCACCGTGAGCAAGCTGCCTGCGGAGCCCCCAGCATTGCTCCAGACACACCCACC A G AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57105626..57105847 26863196 MeRIP-seq:(Medium) rs751741026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903808,Human_RBP_ID_18703163,Human_RBP_ID_22443804,Human_RBP_ID_23736531 Human_miRNA_ID_1546989,Human_miRNA_ID_2396083,Human_miRNA_ID_2685861,Human_miRNA_ID_3069948 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 97701 RMVar_ID_97701 Human_SNP_ID_628252808 m1A Human chr17 + 57106452 57106410 57106452 GAAATGAGGAGGGCTTGGATAGAAATGAGGAGAGCTTGGATAGAAATGAGGAGGGCTTGGATAGA _________________________________GCTTGGATAGAAATGAGGAGGGCTTGGATAGA GGCTTGGATAGAAATGAGGAGGGCTTGGATAGAAATGAGGAGA G AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs772342174 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_6429,Human_RBP_ID_6617075,Human_RBP_ID_13083726,Human_RBP_ID_23118777,Human_RBP_ID_23736534,Human_RBP_ID_26332113 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 97702 RMVar_ID_97702 Human_SNP_ID_628252818 m1A Human chr17 + 57106452 57106431 57106452 GAAATGAGGAGGGCTTGGATAGAAATGAGGAGAGCTTGGATAGAAATGAGGAGGGCTTGGATAGA GAAATGAGGAGG_____________________GCTTGGATAGAAATGAGGAGGGCTTGGATAGA GGCTTGGATAGAAATGAGGAGA G AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs760786475 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_6429,Human_RBP_ID_6617075,Human_RBP_ID_13083726,Human_RBP_ID_23118777,Human_RBP_ID_23736534,Human_RBP_ID_26332113 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 97703 RMVar_ID_97703 Human_SNP_ID_628252829 m1A Human chr17 + 57106452 57106452 57106452 GAAATGAGGAGGGCTTGGATAGAAATGAGGAGAGCTTGGATAGAAATGAGGAGGGCTTGGATAGA GAAATGAGGAGGGCTTGGATAGAAATGAGGAGCGCTTGGATAGAAATGAGGAGGGCTTGGATAGA A C AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34535433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6429,Human_RBP_ID_6617075,Human_RBP_ID_13083726,Human_RBP_ID_23118777,Human_RBP_ID_23736534,Human_RBP_ID_26332113 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 97704 RMVar_ID_97704 Human_SNP_ID_628252830 m1A Human chr17 + 57106452 57106452 57106452 GAAATGAGGAGGGCTTGGATAGAAATGAGGAGAGCTTGGATAGAAATGAGGAGGGCTTGGATAGA GAAATGAGGAGGGCTTGGATAGAAATGAGGAGGGCTTGGATAGAAATGAGGAGGGCTTGGATAGA A G AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34535433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6429,Human_RBP_ID_6617075,Human_RBP_ID_13083726,Human_RBP_ID_23118777,Human_RBP_ID_23736534,Human_RBP_ID_26332113 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 97705 RMVar_ID_97705 Human_SNP_ID_628288603 m1A Human chr17 + 57255910 57255910 57255910 AGGAAAATAAAACTTGTGGCTGGTGTTTGTGCAGGAGGGTCTCCGCCATCCTGAAGCCCCCCGAT AGGAAAATAAAACTTGTGGCTGGTGTTTGTGCGGGAGGGTCTCCGCCATCCTGAAGCCCCCCGAT A G MSI2 Ensembl:ENSG00000153944 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57255860..57256033 26863196 MeRIP-seq:(Medium) rs1395434032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1844335 97706 RMVar_ID_97706 Human_SNP_ID_628288925 m1A Human chr17 + 57256786 57256786 57256786 TGGGAGCCAAGGCACCTCGGGCAGCGCCAACGACTCCCAGCACGACCCCGGGTAAGTTTCCAGCC TGGGAGCCAAGGCACCTCGGGCAGCGCCAACGGCTCCCAGCACGACCCCGGGTAAGTTTCCAGCC A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:57256551..57256887;chr17:57256726..57256847;chr17:57256516..57256871 26863196 MeRIP-seq:(Medium) rs1312566338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3950875,Human_RBP_ID_8191282,Human_RBP_ID_8941910,Human_RBP_ID_9422413,Human_RBP_ID_18419667,Human_RBP_ID_18439340,Human_RBP_ID_18941906,Human_RBP_ID_18988863,Human_RBP_ID_21890228,Human_RBP_ID_23210046,Human_RBP_ID_27812929 Human_Splice_Rec_1844361,Human_Splice_Rec_1844387,Human_Splice_Rec_1844399,Human_Splice_Rec_1844409 97707 RMVar_ID_97707 Human_SNP_ID_628289071 m1A Human chr17 - 57257080 57257079 57257081 CCGATAAACATTTTACTAGAGGGAGAAAACATAACAGAAGTGAGCACCGATGTCAGATCGGCCAT CCGATAAACATTTTACTAGAGGGAGAAAACA__ACAGAAGTGAGCACCGATGTCAGATCGGCCAT TTA T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:57257076..57257150 26863196 MeRIP-seq:(Medium) rs1491347874 Functional Loss DEL dbSNP153 32..33 33 - - - 97708 RMVar_ID_97708 Human_SNP_ID_628289478 m1A Human chr17 - 57258253 57258253 57258253 GACGAAACCGAAGCCTCTGAAAGGAGACAAAGAGGGAGAAAAACAAACAAGAAAATGTGACACCA GACGAAACCGAAGCCTCTGAAAGGAGACAAAGCGGGAGAAAAACAAACAAGAAAATGTGACACCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:57258251..57258300 26863196 MeRIP-seq:(Medium) rs1197595754 Functional Loss SNV dbSNP153 33..33 33 - - - 97709 RMVar_ID_97709 Human_SNP_ID_628289494 m1A Human chr17 - 57258319 57258316 57258319 CTTGGAATCTAACTCATGGTGGGGCTGACCTAATACTTTATCTACACTTGCTGGGTCTGCGAACG CTTGGAATCTAACTCATGGTGGGGCTGACCTA___CTTTATCTACACTTGCTGGGTCTGCGAACG GTAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57258251..57258375 26863196 MeRIP-seq:(Medium) rs752982551 Functional Loss DEL dbSNP153 33..35 33 - - - 97710 RMVar_ID_97710 Human_SNP_ID_628293428 m1A Human chr17 + 57275648 57275648 57275648 ACTTCATGTCCACTGGGTGGAATTTACCAGGTATTGCTGGGAACGGGGAACAAGATCATGATTAT ACTTCATGTCCACTGGGTGGAATTTACCAGGTTTTGCTGGGAACGGGGAACAAGATCATGATTAT A T MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:57275646..57275742 26863196 MeRIP-seq:(Medium) rs1446061870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6617261 RMVar_hsa_circ_11108,RMVar_hsa_circ_315956,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185579,RMVar_hsa_circ_185580,RMVar_hsa_circ_359076,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581 97711 RMVar_ID_97711 Human_SNP_ID_628293432 m1A Human chr17 + 57275664 57275664 57275664 GTGGAATTTACCAGGTATTGCTGGGAACGGGGAACAAGATCATGATTATAAGTGGATCCTGGACA GTGGAATTTACCAGGTATTGCTGGGAACGGGGCACAAGATCATGATTATAAGTGGATCCTGGACA A C MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57275659..57275813 26863196 MeRIP-seq:(Medium) rs1264678534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1537829,Human_RBP_ID_2514022 RMVar_hsa_circ_11108,RMVar_hsa_circ_315956,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185579,RMVar_hsa_circ_185580,RMVar_hsa_circ_359076,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581 97712 RMVar_ID_97712 Human_SNP_ID_628294526 m1A Human chr17 + 57280077 57280077 57280077 TTTTGGGAAGGCTTCCTGGAGAAATAACGTTGAGGCTGAGCTTGATGTAGGGAGGGAAGTAGCAG TTTTGGGAAGGCTTCCTGGAGAAATAACGTTGCGGCTGAGCTTGATGTAGGGAGGGAAGTAGCAG A C MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57280074..57280173 26863196 MeRIP-seq:(Medium) rs1233966877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6617311,Human_RBP_ID_13085144,Human_RBP_ID_22805693 RMVar_hsa_circ_11108,RMVar_hsa_circ_315956,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185579,RMVar_hsa_circ_185580,RMVar_hsa_circ_359076,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581 97713 RMVar_ID_97713 Human_SNP_ID_628296902 m1A Human chr17 - 57289978 57289976 57289978 ACAACCACCTTCTTTGGTTCTAAGCAAAAGAGAGGCAAAAGTCACCAAGACATCATGGGCTCCGC ACAACCACCTTCTTTGGTTCTAAGCAAAAGAG__GCAAAAGTCACCAAGACATCATGGGCTCCGC CCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57289974..57290110 26863196 MeRIP-seq:(Medium) rs140981544 Functional Loss DEL dbSNP153 33..34 33 - - - 97714 RMVar_ID_97714 Human_SNP_ID_628297400 m1A Human chr17 - 57292128 57292128 57292128 AGGCAGCTGTCCGAGGGTCTCCCTAGCCCCCAATCCACTGGACCTTCTCGGTGAATGCGTCCCCT AGGCAGCTGTCCGAGGGTCTCCCTAGCCCCCAGTCCACTGGACCTTCTCGGTGAATGCGTCCCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57292126..57292520 26863196 MeRIP-seq:(Medium) rs937103376 Functional Loss SNV dbSNP153 33..33 33 - - - 97715 RMVar_ID_97715 Human_SNP_ID_628298109 m1A Human chr17 - 57294859 57294859 57294859 CCTGGCCTGCACCCAACCCAGAGCAGGGGATCAAGAAATGTTTGCTCAATGAATGAACCCAACTC CCTGGCCTGCACCCAACCCAGAGCAGGGGATCGAGAAATGTTTGCTCAATGAATGAACCCAACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57294855..57294972 26863196 MeRIP-seq:(Medium) rs916151354 Functional Loss SNV dbSNP153 33..33 33 - - - 97716 RMVar_ID_97716 Human_SNP_ID_628303479 m1A Human chr17 - 57318569 57318569 57318569 CAGCACCCTCTGCCTTCAAGCTTCTTATGAGCAGCACCAACGCCCCAACCCTGACACAGCCCACA CAGCACCCTCTGCCTTCAAGCTTCTTATGAGCGGCACCAACGCCCCAACCCTGACACAGCCCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57318567..57318682 26863196 MeRIP-seq:(Medium) rs1368155262 Functional Loss SNV dbSNP153 33..33 33 - - - 97717 RMVar_ID_97717 Human_SNP_ID_628311900 m1A Human chr17 + 57354681 57354681 57354681 TGAACCTCCAGGAAGTGCAGGTGAGAGCAGAGAGGGTGTGATGAGGAAGGGGGTGGGAGAGGAGT TGAACCTCCAGGAAGTGCAGGTGAGAGCAGAGCGGGTGTGATGAGGAAGGGGGTGGGAGAGGAGT A C MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:57354679..57354804 26863196 MeRIP-seq:(Medium) rs1567776296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11108,RMVar_hsa_circ_315956,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185579,RMVar_hsa_circ_185580,RMVar_hsa_circ_359076,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581 97718 RMVar_ID_97718 Human_SNP_ID_628333218 m1A Human chr17 - 57446176 57446176 57446176 CCCAGAGATGCCTCTCTGAAGGCTATGCCTAAATCGACACCCTCACACACACCCCACCCCACTCC CCCAGAGATGCCTCTCTGAAGGCTATGCCTAAGTCGACACCCTCACACACACCCCACCCCACTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57446174..57446313 26863196 MeRIP-seq:(Medium) rs1485968778 Functional Loss SNV dbSNP153 33..33 33 - - - 97719 RMVar_ID_97719 Human_SNP_ID_628336785 m1A Human chr17 + 57460336 57460336 57460336 ACAGAGCCAAACCCTGTCTTGGGAAGGAAAGAAGGCAGGAAGTTAGGGAGGGAAAGAGAAAAAGG ACAGAGCCAAACCCTGTCTTGGGAAGGAAAGACGGCAGGAAGTTAGGGAGGGAAAGAGAAAAAGG A C MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57460330..57460659 26863196 MeRIP-seq:(Medium) rs772950529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22247,RMVar_hsa_circ_11108,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185580,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581,RMVar_hsa_circ_63952,RMVar_hsa_circ_349018,RMVar_hsa_circ_45245 97720 RMVar_ID_97720 Human_SNP_ID_628343052 m1A Human chr17 + 57486968 57486968 57486968 AATACAAGGCAAGTAAGTACTGGGTGCATGCAAAGTGCTTTGGGATTGTAAAAGAGAAAGAGAAA AATACAAGGCAAGTAAGTACTGGGTGCATGCAGAGTGCTTTGGGATTGTAAAAGAGAAAGAGAAA A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57486966..57487037 26863196 MeRIP-seq:(Medium) rs1013928603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2514973 RMVar_hsa_circ_22247,RMVar_hsa_circ_11108,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185580,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581,RMVar_hsa_circ_63952,RMVar_hsa_circ_349018,RMVar_hsa_circ_45245 97721 RMVar_ID_97721 Human_SNP_ID_628381984 m1A Human chr17 + 57649732 57649732 57649732 TTTGGCGGGTGAGGGGTGACTGGTGAGGCTGGATGGCCTAATGGAACAGGAGGGGGATGGCGAGG TTTGGCGGGTGAGGGGTGACTGGTGAGGCTGGTTGGCCTAATGGAACAGGAGGGGGATGGCGAGG A T MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57649724..57649791 26863196 MeRIP-seq:(Medium) rs1056173102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200098,Human_RBP_ID_1066624,Human_RBP_ID_5187442,Human_RBP_ID_9422947,Human_RBP_ID_26758362 RMVar_hsa_circ_11108,RMVar_hsa_circ_372858,RMVar_hsa_circ_185580,RMVar_hsa_circ_92033,RMVar_hsa_circ_185589,RMVar_hsa_circ_346042,RMVar_hsa_circ_267516 97722 RMVar_ID_97722 Human_SNP_ID_628388814 m1A Human chr17 + 57679661 57679661 57679661 CCCACCAGCCTCACTCCCCATCCCAACCAGAGATGGCTCACTTCGGATCGAGGGTTGACTACATC CCCACCAGCCTCACTCCCCATCCCAACCAGAGGTGGCTCACTTCGGATCGAGGGTTGACTACATC A G MSI2 Ensembl:ENSG00000153944 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57679614..57679706 26863196 MeRIP-seq:(Medium) rs1050459007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_494827,Human_RBP_ID_6618321,Human_RBP_ID_9073971,Human_RBP_ID_9378606,Human_RBP_ID_23737638 RMVar_hsa_circ_92033,RMVar_hsa_circ_185589,RMVar_hsa_circ_98755,RMVar_hsa_circ_185593 97723 RMVar_ID_97723 Human_SNP_ID_628389866 m1A Human chr17 - 57683806 57683806 57683806 GCTGACGTCTGCTAGTTTTCTGCTTTGGGGTGAGGGTGGGGAAACCCGCCAGTGTCTTTCTTCAA GCTGACGTCTGCTAGTTTTCTGCTTTGGGGTGGGGGTGGGGAAACCCGCCAGTGTCTTTCTTCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57683757..57683850 26863196 MeRIP-seq:(Medium) rs1016235535 Functional Loss SNV dbSNP153 33..33 33 - - - 97724 RMVar_ID_97724 Human_SNP_ID_628426628 m1A Human chr17 + 57835427 57835424 57835427 TGACATGTCTCCTCTTTCCTCCTTCCCTGCCCACTCCTCCATCCCATTCTTTACATCACTCCTAG TGACATGTCTCCTCTTTCCTCCTTCCCTGC___CTCCTCCATCCCATTCTTTACATCACTCCTAG CCCA C lnc-MSI2-5 RNACentral:URS00008B6B6C lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:57835387..57835488 26863196 MeRIP-seq:(Medium) rs1220462098 Functional Loss DEL dbSNP153 31..33 33 - - - 97725 RMVar_ID_97725 Human_SNP_ID_628430795 m1A Human chr17 - 57850005 57850005 57850005 AGTCACGCTCGGTACCAGGCGCAGATCATGGCAGGCAGCCGGCTGGAAACCGTAGGGAGCATCTT AGTCACGCTCGGTACCAGGCGCAGATCATGGCGGGCAGCCGGCTGGAAACCGTAGGGAGCATCTT T C MRPS23 Ensembl:ENSG00000181610 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57849923..57850025 26863196 MeRIP-seq:(Medium) rs775066859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766420,Human_RBP_ID_4465563,Human_RBP_ID_5497435,Human_RBP_ID_22444790,Human_RBP_ID_22499980 Human_Splice_Rec_1844539,Human_Splice_Rec_1844547,Human_Splice_Rec_1844559 Human_miRNA_ID_2974815,Human_miRNA_ID_3008011 RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 97726 RMVar_ID_97726 Human_SNP_ID_628430796 m1A Human chr17 - 57850005 57850005 57850005 AGTCACGCTCGGTACCAGGCGCAGATCATGGCAGGCAGCCGGCTGGAAACCGTAGGGAGCATCTT AGTCACGCTCGGTACCAGGCGCAGATCATGGCCGGCAGCCGGCTGGAAACCGTAGGGAGCATCTT T G MRPS23 Ensembl:ENSG00000181610 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57849923..57850025 26863196 MeRIP-seq:(Medium) rs775066859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766420,Human_RBP_ID_4465563,Human_RBP_ID_5497435,Human_RBP_ID_22444790,Human_RBP_ID_22499980 Human_Splice_Rec_1844539,Human_Splice_Rec_1844547,Human_Splice_Rec_1844559 Human_miRNA_ID_2974815,Human_miRNA_ID_3008011 RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 97727 RMVar_ID_97727 Human_SNP_ID_628430807 m1A Human chr17 - 57850015 57850015 57850015 GGTAGCAGCTAGTCACGCTCGGTACCAGGCGCAGATCATGGCAGGCAGCCGGCTGGAAACCGTAG GGTAGCAGCTAGTCACGCTCGGTACCAGGCGCTGATCATGGCAGGCAGCCGGCTGGAAACCGTAG T A MRPS23 Ensembl:ENSG00000181610 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:57849915..57850050;chr17:57849911..57850050 26863196 MeRIP-seq:(Medium) rs750665058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766420,Human_RBP_ID_4465563,Human_RBP_ID_5497435,Human_RBP_ID_22444790,Human_RBP_ID_22499980 Human_Splice_Rec_1844539,Human_Splice_Rec_1844547,Human_Splice_Rec_1844559 Human_miRNA_ID_2974815 RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 97728 RMVar_ID_97728 Human_SNP_ID_628434311 m1A Human chr17 + 57862180 57862180 57862180 GGTCTGCGCGCTCCCATGTCCAGGGCGGGGCCACGGGCTGGGCAGCCTCCCTCCCCGTGGCAGTG GGTCTGCGCGCTCCCATGTCCAGGGCGGGGCCGCGGGCTGGGCAGCCTCCCTCCCCGTGGCAGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57862134..57862474 26863196 MeRIP-seq:(Medium) rs1170391298 Functional Loss SNV dbSNP153 33..33 33 - - - 97729 RMVar_ID_97729 Human_SNP_ID_628434352 m1A Human chr17 + 57862315 57862315 57862315 CCAGCAAGCCCTTATGCCCTAGGCGCTCACCCAGGCTGGCGGCCTTTCCGCCTTGCTCTTTAGCC CCAGCAAGCCCTTATGCCCTAGGCGCTCACCCCGGCTGGCGGCCTTTCCGCCTTGCTCTTTAGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57862265..57862412 26863196 MeRIP-seq:(Medium) rs1568022588 Functional Loss SNV dbSNP153 33..33 33 - - - 97730 RMVar_ID_97730 Human_SNP_ID_628438827 m1A Human chr17 + 57879662 57879662 57879662 GAGCCAGAGGGTAGGGCCGGTCGAACACGTGCATGTGGTAGGCTGGCGGGGAGTACACAGGTGGG GAGCCAGAGGGTAGGGCCGGTCGAACACGTGCGTGTGGTAGGCTGGCGGGGAGTACACAGGTGGG A G lnc-MSI2-7 RNACentral:URS0000D57491 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:57879579..57879771;chr17:57879601..57879769 26863196 MeRIP-seq:(Medium) rs779450958 Functional Loss SNV dbSNP153 33..33 33 - - - 97731 RMVar_ID_97731 Human_SNP_ID_628438828 m1A Human chr17 + 57879662 57879662 57879662 GAGCCAGAGGGTAGGGCCGGTCGAACACGTGCATGTGGTAGGCTGGCGGGGAGTACACAGGTGGG GAGCCAGAGGGTAGGGCCGGTCGAACACGTGCTTGTGGTAGGCTGGCGGGGAGTACACAGGTGGG A T lnc-MSI2-7 RNACentral:URS0000D57491 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:57879579..57879771;chr17:57879601..57879769 26863196 MeRIP-seq:(Medium) rs779450958 Functional Loss SNV dbSNP153 33..33 33 - - - 97732 RMVar_ID_97732 Human_SNP_ID_628440153 m1A Human chr17 - 57885196 57885196 57885196 GTAGGGGCGCAGCCCGGGTAATTCCAACCACCACTGGAGGACAGCATCCCCCCGGAGGTAGGGGC GTAGGGGCGCAGCCCGGGTAATTCCAACCACCGCTGGAGGACAGCATCCCCCCGGAGGTAGGGGC T C CUEDC1 Ensembl:ENSG00000180891 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57885194..57885330 26863196 MeRIP-seq:(Medium) rs780419227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121201,RMVar_hsa_circ_372673,RMVar_hsa_circ_185600,RMVar_hsa_circ_78075,RMVar_hsa_circ_185602,RMVar_hsa_circ_185603,RMVar_hsa_circ_376264,RMVar_hsa_circ_185606 97733 RMVar_ID_97733 Human_SNP_ID_628440263 m1A Human chr17 - 57885414 57885414 57885414 GCCAGGTGCGCCGCCTGGAGTTCAACCAGGCCATGGACGACTTCAAGACCATGTTCCCCAACATG GCCAGGTGCGCCGCCTGGAGTTCAACCAGGCCCTGGACGACTTCAAGACCATGTTCCCCAACATG T G CUEDC1 Ensembl:ENSG00000180891 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57885364..57885696 26863196 MeRIP-seq:(Medium) rs773296357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1844682 RMVar_hsa_circ_121201,RMVar_hsa_circ_372673,RMVar_hsa_circ_185600,RMVar_hsa_circ_78075,RMVar_hsa_circ_185602,RMVar_hsa_circ_185603,RMVar_hsa_circ_376264,RMVar_hsa_circ_185606 97734 RMVar_ID_97734 Human_SNP_ID_628446276 m1A Human chr17 - 57911033 57911033 57911033 GTGATCTTTACATAAGAGACTGAGGAGTTCGGAGGGGACCTGGCCTGCTCTTCCGTTGGTGGCAT GTGATCTTTACATAAGAGACTGAGGAGTTCGGGGGGGACCTGGCCTGCTCTTCCGTTGGTGGCAT T C CUEDC1 Ensembl:ENSG00000180891 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:57911020..57911104 26863196 MeRIP-seq:(Medium) rs1183833082 Functional Loss SNV dbSNP153 33..33 33 - - - 97735 RMVar_ID_97735 Human_SNP_ID_628461499 m1A Human chr17 - 57974583 57974583 57974583 ATATAGCACACCCTGTCACCATCACATCTCCAATGAATCTACCCACACCTATGACATTAGCCGCC ATATAGCACACCCTGTCACCATCACATCTCCAGTGAATCTACCCACACCTATGACATTAGCCGCC T C VEZF1 Ensembl:ENSG00000136451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:57974533..57974643;chr17:57974533..57974641 26863196 MeRIP-seq:(Medium) rs766882992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17079697,Human_RBP_ID_18943430 Human_miRNA_ID_1985361,Human_miRNA_ID_2941001 RMVar_hsa_circ_185608,RMVar_hsa_circ_94437,RMVar_hsa_circ_118601,RMVar_hsa_circ_122526,RMVar_hsa_circ_110383,RMVar_hsa_circ_185610,RMVar_hsa_circ_86600,RMVar_hsa_circ_185611,RMVar_hsa_circ_185609,RMVar_hsa_circ_185607 97736 RMVar_ID_97736 Human_SNP_ID_628462626 m1A Human chr17 + 57979225 57979225 57979225 GTTTCTACTTGCTTCCCTGGCCAGCTTGTCACATGTTGTTGTTGTTGTTGTTGCTGCTGCTGCTG GTTTCTACTTGCTTCCCTGGCCAGCTTGTCACGTGTTGTTGTTGTTGTTGTTGCTGCTGCTGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:57979176..57979251 26863196 MeRIP-seq:(Medium) rs1009951435 Functional Loss SNV dbSNP153 33..33 33 - - - 97737 RMVar_ID_97737 Human_SNP_ID_628466559 m1A Human chr17 - 57993820 57993820 57993820 GAGGTAAGGTCAGTAAAACAAAAAGCTAGCAGAGGGCAGGGTCAGGCCCTTGGGGTAGAGGGCTA GAGGTAAGGTCAGTAAAACAAAAAGCTAGCAGCGGGCAGGGTCAGGCCCTTGGGGTAGAGGGCTA T G AC015813.2,AC015813.1 Ensembl:ENSG00000266086,Ensembl:ENSG00000264112 Protein coding,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57993770..57993931 26863196 MeRIP-seq:(Medium) rs1176578078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237338,Human_RBP_ID_766951,Human_RBP_ID_819687,Human_RBP_ID_5088501,Human_RBP_ID_6619236,Human_RBP_ID_8193948,Human_RBP_ID_8232622,Human_RBP_ID_9886971,Human_RBP_ID_13092743,Human_RBP_ID_22954633,Human_RBP_ID_25344725 97738 RMVar_ID_97738 Human_SNP_ID_628466560 m1A Human chr17 - 57993822 57993822 57993822 AGGAGGTAAGGTCAGTAAAACAAAAAGCTAGCAGAGGGCAGGGTCAGGCCCTTGGGGTAGAGGGC AGGAGGTAAGGTCAGTAAAACAAAAAGCTAGCCGAGGGCAGGGTCAGGCCCTTGGGGTAGAGGGC T G AC015813.2,AC015813.1 Ensembl:ENSG00000266086,Ensembl:ENSG00000264112 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:57993773..57993924 26863196 MeRIP-seq:(Medium) rs1437460297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237338,Human_RBP_ID_819687,Human_RBP_ID_5088501,Human_RBP_ID_5188864,Human_RBP_ID_6619236,Human_RBP_ID_8193948,Human_RBP_ID_8232622,Human_RBP_ID_9886971,Human_RBP_ID_13092743,Human_RBP_ID_22954633,Human_RBP_ID_25344725 97739 RMVar_ID_97739 Human_SNP_ID_628466563 m1A Human chr17 - 57993829 57993828 57993829 GAAGTTGAGGAGGTAAGGTCAGTAAAACAAAAAGCTAGCAGAGGGCAGGGTCAGGCCCTTGGGGT GAAGTTGAGGAGGTAAGGTCAGTAAAACAAAA_GCTAGCAGAGGGCAGGGTCAGGCCCTTGGGGT CT C AC015813.2,AC015813.1 Ensembl:ENSG00000266086,Ensembl:ENSG00000264112 Protein coding,lincRNA intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:57993780..57993901 26863196 MeRIP-seq:(Medium) rs1178644792 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_237338,Human_RBP_ID_819687,Human_RBP_ID_5088501,Human_RBP_ID_5188864,Human_RBP_ID_8232622,Human_RBP_ID_9886971,Human_RBP_ID_13092743,Human_RBP_ID_22954633,Human_RBP_ID_25344725 97740 RMVar_ID_97740 Human_SNP_ID_628469292 m1A Human chr17 - 58003953 58003953 58003953 GCTCACTGGATCCCAATCCTTGGAGCTGGATCATTGGATTCAAATCATAATGTGGATAGGATAGG GCTCACTGGATCCCAATCCTTGGAGCTGGATCGTTGGATTCAAATCATAATGTGGATAGGATAGG T C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:58003876..58004062 26863196 MeRIP-seq:(Medium) rs1287819884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48251,Human_RBP_ID_495218,Human_RBP_ID_1009464,Human_RBP_ID_1090903,Human_RBP_ID_1183165,Human_RBP_ID_1538209,Human_RBP_ID_1863997,Human_RBP_ID_2515670,Human_RBP_ID_3529989,Human_RBP_ID_4476388,Human_RBP_ID_6619552,Human_RBP_ID_8193038,Human_RBP_ID_8458171,Human_RBP_ID_9074106,Human_RBP_ID_9887088,Human_RBP_ID_13093387,Human_RBP_ID_17260998,Human_RBP_ID_17376724,Human_RBP_ID_17492651,Human_RBP_ID_17692622,Human_RBP_ID_17897030,Human_RBP_ID_18164806,Human_RBP_ID_18294458,Human_RBP_ID_18703649,Human_RBP_ID_22805810,Human_RBP_ID_22959638,Human_RBP_ID_23275952,Human_RBP_ID_23738184,Human_RBP_ID_25344865,Human_RBP_ID_26460780,Human_RBP_ID_27667463 Human_Splice_Rec_1844734,Human_Splice_Rec_1844762,Human_Splice_Rec_1844768 RMVar_hsa_circ_76095,RMVar_hsa_circ_185617,RMVar_hsa_circ_185616 97741 RMVar_ID_97741 Human_SNP_ID_628469698 m1A Human chr17 - 58005848 58005848 58005848 GTGTCGTGGAGTTTGTACGGAAAGAAGATATGACCTATGCAGTTCGAAAACTGGATAACACTAAG GTGTCGTGGAGTTTGTACGGAAAGAAGATATGGCCTATGCAGTTCGAAAACTGGATAACACTAAG T C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1198381764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495288,Human_RBP_ID_902541,Human_RBP_ID_1538249,Human_RBP_ID_1864022,Human_RBP_ID_2515729,Human_RBP_ID_3530012,Human_RBP_ID_5577583,Human_RBP_ID_6619706,Human_RBP_ID_9376440,Human_RBP_ID_13093529,Human_RBP_ID_18703697,Human_RBP_ID_18991863,Human_RBP_ID_22061539,Human_RBP_ID_22218031,Human_RBP_ID_22805865,Human_RBP_ID_22959457,Human_RBP_ID_23738239,Human_RBP_ID_24545226,Human_RBP_ID_25304922,Human_RBP_ID_26330809,Human_RBP_ID_26967244,Human_RBP_ID_27257385,Human_RBP_ID_27667501,Human_RBP_ID_27812932 Human_Splice_Rec_1844747,Human_Splice_Rec_1844757,Human_Splice_Rec_1844773,Human_Splice_Rec_1844785 Human_miRNA_ID_1563567,Human_miRNA_ID_1749050,Human_miRNA_ID_2093573,Human_miRNA_ID_2235383,Human_miRNA_ID_3029547 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616,RMVar_hsa_circ_359101 97742 RMVar_ID_97742 Human_SNP_ID_628469715 m1A Human chr17 + 58005966 58005966 58005966 TGATCCTTTAAATCCTGCCAACTTCCACTTGGAGGCAGTCCTGAAAAAGTGATTTTTTTTTTCTT TGATCCTTTAAATCCTGCCAACTTCCACTTGGGGGCAGTCCTGAAAAAGTGATTTTTTTTTTCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58005846..58005975 26863196 MeRIP-seq:(Medium) rs763505486 Functional Loss SNV dbSNP153 33..33 33 - - - 97743 RMVar_ID_97743 Human_SNP_ID_628469830 m1A Human chr17 - 58006304 58006304 58006304 GTACTGGTTGTGTGGATTGATGTGAAGGGACGAAAACTACCTAAAATTTTTCTCTTGCGTGACAG GTACTGGTTGTGTGGATTGATGTGAAGGGACGGAAACTACCTAAAATTTTTCTCTTGCGTGACAG T C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58006301..58006325 32194978 MeRIP-seq:(Medium) rs889542941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1538255,Human_RBP_ID_5367519,Human_RBP_ID_22954877,Human_RBP_ID_23738249 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616,RMVar_hsa_circ_359101 97744 RMVar_ID_97744 Human_SNP_ID_628469866 m1A Human chr17 + 58006416 58006416 58006416 CCATAGCGACCTCGGGGAGCTCCGCCACCTCCACCCCCGCCGCCGCCTCGGCCTGTTCCACGGCC CCATAGCGACCTCGGGGAGCTCCGCCACCTCCCCCCCCGCCGCCGCCTCGGCCTGTTCCACGGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:58006324..58006560;chr17:58006368..58006575 26863196,32194978 MeRIP-seq:(Medium) rs528540802 Functional Loss SNV dbSNP153 33..33 33 - - - 97745 RMVar_ID_97745 Human_SNP_ID_628469877 m1A Human chr17 - 58006440 58006440 58006440 CTGCGGGTGGAGTTTCCTCGAAGCGGCCGTGGAACAGGCCGAGGCGGCGGCGGGGGTGGAGGTGG CTGCGGGTGGAGTTTCCTCGAAGCGGCCGTGGGACAGGCCGAGGCGGCGGCGGGGGTGGAGGTGG T C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58006391..58006537 26863196 MeRIP-seq:(Medium) rs916383308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48261,Human_RBP_ID_495292,Human_RBP_ID_765365,Human_RBP_ID_820699,Human_RBP_ID_1538257,Human_RBP_ID_4476431,Human_RBP_ID_5577584,Human_RBP_ID_9378637,Human_RBP_ID_13093547,Human_RBP_ID_17897075,Human_RBP_ID_18703706,Human_RBP_ID_18991868,Human_RBP_ID_22218039,Human_RBP_ID_22805875,Human_RBP_ID_23738251,Human_RBP_ID_24415651 Human_Splice_Rec_1844730,Human_Splice_Rec_1844731,Human_Splice_Rec_1844744,Human_Splice_Rec_1844745,Human_Splice_Rec_1844750,Human_Splice_Rec_1844751,Human_Splice_Rec_1844755,Human_Splice_Rec_1844764,Human_Splice_Rec_1844765,Human_Splice_Rec_1844770,Human_Splice_Rec_1844771,Human_Splice_Rec_1844778,Human_Splice_Rec_1844782,Human_Splice_Rec_1844783,Human_Splice_Rec_1844788 Human_miRNA_ID_1979528 RMVar_hsa_circ_3920,RMVar_hsa_circ_76095,RMVar_hsa_circ_185616,RMVar_hsa_circ_359101 97746 RMVar_ID_97746 Human_SNP_ID_628469983 m1A Human chr17 - 58006699 58006696 58006699 GAGCGGGAAACTGAGGCGCTGAGGGCTGGTGTAGTGGTTGGGAGCCTGGCGTGTTTCTGGGTGGG GAGCGGGAAACTGAGGCGCTGAGGGCTGGTGT___GGTTGGGAGCCTGGCGTGTTTCTGGGTGGG CACT C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58006696..58006869 26863196 MeRIP-seq:(Medium) rs1368901091 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1287741,Human_RBP_ID_1538261,Human_RBP_ID_13093552,Human_RBP_ID_18941931,Human_RBP_ID_21974456,Human_RBP_ID_22475385,Human_RBP_ID_22657650,Human_RBP_ID_23738255,Human_RBP_ID_25304961 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616 97747 RMVar_ID_97747 Human_SNP_ID_628469985 m1A Human chr17 + 58006702 58006702 58006702 ACCCAGAAACACGCCAGGCTCCCAACCACTACACCAGCCCTCAGCGCCTCAGTTTCCCGCTCCAG ACCCAGAAACACGCCAGGCTCCCAACCACTACGCCAGCCCTCAGCGCCTCAGTTTCCCGCTCCAG A G AC015813.5 Ensembl:ENSG00000279069 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58006700..58006813 26863196 MeRIP-seq:(Medium) rs977824264 Functional Loss SNV dbSNP153 33..33 33 - - - 97748 RMVar_ID_97748 Human_SNP_ID_628470124 m1A Human chr17 + 58007148 58007148 58007148 GAATCACACCACCTCCCGACATGGCGGTGACGAAAAGCGCGGACTCGAGAACAGGCCTTCCCACC GAATCACACCACCTCCCGACATGGCGGTGACGCAAAGCGCGGACTCGAGAACAGGCCTTCCCACC A C AC015813.5 Ensembl:ENSG00000279069 Other exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:58007051..58007250 26863410 MeRIP-seq:(Medium) rs561675206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3196330 97749 RMVar_ID_97749 Human_SNP_ID_628470138 m1A Human chr17 + 58007166 58007166 58007166 ACATGGCGGTGACGAAAAGCGCGGACTCGAGAACAGGCCTTCCCACCAAGCCTAGCGCACGGCAG ACATGGCGGTGACGAAAAGCGCGGACTCGAGAGCAGGCCTTCCCACCAAGCCTAGCGCACGGCAG A G AC015813.5 Ensembl:ENSG00000279069 Other exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:58007046..58007216 26863410 MeRIP-seq:(Medium) rs752176246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3148851,Human_miRNA_ID_3196330 97750 RMVar_ID_97750 Human_SNP_ID_628470152 m1A Human chr17 + 58007182 58007182 58007182 AAGCGCGGACTCGAGAACAGGCCTTCCCACCAAGCCTAGCGCACGGCAGAGCGAGCCCGCAGCGG AAGCGCGGACTCGAGAACAGGCCTTCCCACCAGGCCTAGCGCACGGCAGAGCGAGCCCGCAGCGG A G AC015813.5 Ensembl:ENSG00000279069 Other exon GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:58007051..58007250 26863410 MeRIP-seq:(Medium) rs771573596 Functional Loss SNV dbSNP153 33..33 33 - - - 97751 RMVar_ID_97751 Human_SNP_ID_628470165 m1A Human chr17 + 58007197 58007197 58007197 AACAGGCCTTCCCACCAAGCCTAGCGCACGGCAGAGCGAGCCCGCAGCGGCACCACGTCTCCCGC AACAGGCCTTCCCACCAAGCCTAGCGCACGGCCGAGCGAGCCCGCAGCGGCACCACGTCTCCCGC A C AC015813.5 Ensembl:ENSG00000279069 Other exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:58007096..58007211 26863410 MeRIP-seq:(Medium) rs1033069573 Functional Loss SNV dbSNP153 33..33 33 - - - 97752 RMVar_ID_97752 Human_SNP_ID_628470178 m1A Human chr17 + 58007210 58007210 58007210 ACCAAGCCTAGCGCACGGCAGAGCGAGCCCGCAGCGGCACCACGTCTCCCGCGGCCCCTCCAAAA ACCAAGCCTAGCGCACGGCAGAGCGAGCCCGCCGCGGCACCACGTCTCCCGCGGCCCCTCCAAAA A C AC015813.5 Ensembl:ENSG00000279069 Other exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:58007026..58007275;chr17:58006901..58007275;chr17:58006703..58007275;chr17:58007021..58007275 26863196 MeRIP-seq:(Medium) rs1412370395 Functional Loss SNV dbSNP153 33..33 33 - - - 97753 RMVar_ID_97753 Human_SNP_ID_628470184 m1A Human chr17 + 58007216 58007216 58007216 CCTAGCGCACGGCAGAGCGAGCCCGCAGCGGCACCACGTCTCCCGCGGCCCCTCCAAAATGGCGC CCTAGCGCACGGCAGAGCGAGCCCGCAGCGGCGCCACGTCTCCCGCGGCCCCTCCAAAATGGCGC A G AC015813.5 Ensembl:ENSG00000279069 Other exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58006869..58007275 26863196 MeRIP-seq:(Medium) rs1234783048 Functional Loss SNV dbSNP153 33..33 33 - - - 97754 RMVar_ID_97754 Human_SNP_ID_628488898 m1A Human chr17 + 58083514 58083514 58083514 GAGGCGGAGCGCGGGCGGCCGGCGAAACTCCAAGGGCGGACCGCGGCAGGGAGCGATCGGCCTCG GAGGCGGAGCGCGGGCGGCCGGCGAAACTCCAGGGGCGGACCGCGGCAGGGAGCGATCGGCCTCG A G DYNLL2 Ensembl:ENSG00000264364 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:58083476..58083632 26863196 MeRIP-seq:(Medium) rs1357912416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541808,Human_RBP_ID_4464686,Human_RBP_ID_5143297,Human_RBP_ID_5318487,Human_RBP_ID_5467581,Human_RBP_ID_8192144,Human_RBP_ID_9289244,Human_RBP_ID_9326761,Human_RBP_ID_9376445,Human_RBP_ID_9422433,Human_RBP_ID_18419673,Human_RBP_ID_23738280,Human_RBP_ID_24372988,Human_RBP_ID_26332125 Human_miRNA_ID_1967919,Human_miRNA_ID_2616099 RMVar_hsa_circ_83104,RMVar_hsa_circ_185619 97755 RMVar_ID_97755 Human_SNP_ID_628488900 m1A Human chr17 + 58083521 58083521 58083521 AGCGCGGGCGGCCGGCGAAACTCCAAGGGCGGACCGCGGCAGGGAGCGATCGGCCTCGGGCTGCG AGCGCGGGCGGCCGGCGAAACTCCAAGGGCGGTCCGCGGCAGGGAGCGATCGGCCTCGGGCTGCG A T DYNLL2 Ensembl:ENSG00000264364 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:58083426..58083550 26863410 MeRIP-seq:(Medium) rs1186617462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4441226,Human_RBP_ID_5143297,Human_RBP_ID_5318487,Human_RBP_ID_5467581,Human_RBP_ID_9327374,Human_RBP_ID_9376445,Human_RBP_ID_9422433,Human_RBP_ID_18419673,Human_RBP_ID_23738280,Human_RBP_ID_26332125 RMVar_hsa_circ_83104,RMVar_hsa_circ_185619 97756 RMVar_ID_97756 Human_SNP_ID_628488905 m1A Human chr17 + 58083533 58083533 58083533 CGGCGAAACTCCAAGGGCGGACCGCGGCAGGGAGCGATCGGCCTCGGGCTGCGGGAGCCGGAGAC CGGCGAAACTCCAAGGGCGGACCGCGGCAGGGGGCGATCGGCCTCGGGCTGCGGGAGCCGGAGAC A G DYNLL2 Ensembl:ENSG00000264364 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:58083433..58083700 26863410 MeRIP-seq:(Medium) rs1446387850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237214,Human_RBP_ID_1009513,Human_RBP_ID_4441226,Human_RBP_ID_5143297,Human_RBP_ID_5318487,Human_RBP_ID_5466747,Human_RBP_ID_9327374,Human_RBP_ID_9376445,Human_RBP_ID_9422948,Human_RBP_ID_18419673,Human_RBP_ID_22443072,Human_RBP_ID_23738280,Human_RBP_ID_26332125 RMVar_hsa_circ_83104,RMVar_hsa_circ_185619 97757 RMVar_ID_97757 Human_SNP_ID_628490644 m1A Human chr17 - 58089677 58089677 58089677 TCCCAAAGCAGCATCCACCGCCAGGAAGAGGCAGCTGCACAGTTTTAGTTCCACCTCCAGAGACC TCCCAAAGCAGCATCCACCGCCAGGAAGAGGCGGCTGCACAGTTTTAGTTCCACCTCCAGAGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58089626..58090023 26863196 MeRIP-seq:(Medium) rs941836303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98177,RMVar_hsa_circ_185622 97758 RMVar_ID_97758 Human_SNP_ID_628490650 m1A Human chr17 + 58089696 58089696 58089696 AAAACTGTGCAGCTGCCTCTTCCTGGCGGTGGATGCTGCTTTGGGAGGGCCAGGGAGGCTGCAGG AAAACTGTGCAGCTGCCTCTTCCTGGCGGTGGGTGCTGCTTTGGGAGGGCCAGGGAGGCTGCAGG A G DYNLL2 Ensembl:ENSG00000264364 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58089645..58089924 26863196 MeRIP-seq:(Medium) rs903742889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495317,Human_RBP_ID_4441262,Human_RBP_ID_6619810,Human_RBP_ID_9353327,Human_RBP_ID_23738310 Human_miRNA_ID_42329,Human_miRNA_ID_71046,Human_miRNA_ID_930899,Human_miRNA_ID_1938302,Human_miRNA_ID_1949402,Human_miRNA_ID_2087115,Human_miRNA_ID_2102066,Human_miRNA_ID_2108023,Human_miRNA_ID_2113961,Human_miRNA_ID_2166506,Human_miRNA_ID_2427628,Human_miRNA_ID_2431989,Human_miRNA_ID_2597763,Human_miRNA_ID_2740669,Human_miRNA_ID_3041255 RMVar_hsa_circ_91006,RMVar_hsa_circ_83104,RMVar_hsa_circ_185619,RMVar_hsa_circ_92078,RMVar_hsa_circ_185620,RMVar_hsa_circ_185621 97759 RMVar_ID_97759 Human_SNP_ID_628490663 m1A Human chr17 + 58089750 58089750 58089750 GAGGCTGCAGGGGGACAGTGTTGGGATTGTCAAGGAAAAAGGGGTAGGAAGGAAGGTGGAGGGAT GAGGCTGCAGGGGGACAGTGTTGGGATTGTCAGGGAAAAAGGGGTAGGAAGGAAGGTGGAGGGAT A G DYNLL2 Ensembl:ENSG00000264364 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:58089531..58090073 26863196 MeRIP-seq:(Medium) rs1007248721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495319,Human_RBP_ID_1009519,Human_RBP_ID_6619813,Human_RBP_ID_9353327,Human_RBP_ID_13093842,Human_RBP_ID_22954901,Human_RBP_ID_23738310,Human_RBP_ID_26453725,Human_RBP_ID_27667516 RMVar_hsa_circ_91006,RMVar_hsa_circ_83104,RMVar_hsa_circ_185619,RMVar_hsa_circ_92078,RMVar_hsa_circ_185620,RMVar_hsa_circ_185621 97760 RMVar_ID_97760 Human_SNP_ID_628490887 m1A Human chr17 + 58090566 58090566 58090566 AGTGCAGAGGGACAGTGACTGTGGATGGTTGCAGTCTCTGGTGGGAGGTGAGGATAGAAGTGATA AGTGCAGAGGGACAGTGACTGTGGATGGTTGCCGTCTCTGGTGGGAGGTGAGGATAGAAGTGATA A C DYNLL2 Ensembl:ENSG00000264364 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58090370..58090700 32194978 MeRIP-seq:(Medium) rs540877569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495341,Human_RBP_ID_1092169,Human_RBP_ID_3530059,Human_RBP_ID_6619852,Human_RBP_ID_9353329,Human_RBP_ID_13093865,Human_RBP_ID_17905026,Human_RBP_ID_23129493,Human_RBP_ID_23738346,Human_RBP_ID_27667521 97761 RMVar_ID_97761 Human_SNP_ID_628490888 m1A Human chr17 + 58090566 58090566 58090566 AGTGCAGAGGGACAGTGACTGTGGATGGTTGCAGTCTCTGGTGGGAGGTGAGGATAGAAGTGATA AGTGCAGAGGGACAGTGACTGTGGATGGTTGCGGTCTCTGGTGGGAGGTGAGGATAGAAGTGATA A G DYNLL2 Ensembl:ENSG00000264364 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58090370..58090700 32194978 MeRIP-seq:(Medium) rs540877569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495341,Human_RBP_ID_1092169,Human_RBP_ID_3530059,Human_RBP_ID_6619852,Human_RBP_ID_9353329,Human_RBP_ID_13093865,Human_RBP_ID_17905026,Human_RBP_ID_23129493,Human_RBP_ID_23738346,Human_RBP_ID_27667521 97762 RMVar_ID_97762 Human_SNP_ID_628492199 m1A Human chr17 + 58095842 58095842 58095842 GCCAGAGAAACACAACCAGTAGGATATATTCTATCTTGTCTGTCTTCATATCCATGTATCTGTCA GCCAGAGAAACACAACCAGTAGGATATATTCTGTCTTGTCTGTCTTCATATCCATGTATCTGTCA A G AC015813.6 Ensembl:ENSG00000279207 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2877858 Functional Loss SNV dbSNP153 33..33 33 - - - 97763 RMVar_ID_97763 Human_SNP_ID_628496940 m1A Human chr17 + 58117512 58117512 58117512 GTGTCAGTGATGGTGATGATGGTGATGGTGACAGTGATGATGGTGATGATGGTGATGCTGCCGAT GTGTCAGTGATGGTGATGATGGTGATGGTGACGGTGATGATGGTGATGATGGTGATGCTGCCGAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58117489..58117554 26863196 MeRIP-seq:(Medium) rs917441239 Functional Loss SNV dbSNP153 33..33 33 - - - 97764 RMVar_ID_97764 Human_SNP_ID_628522523 m1A Human chr17 - 58218731 58218731 58218731 TCTGGTAACGAATATTTTGGGCTTTTCTTGACAGAGTCCACCTGCAAAGAATCACATCAAGCAAC TCTGGTAACGAATATTTTGGGCTTTTCTTGACTGAGTCCACCTGCAAAGAATCACATCAAGCAAC T A MKS1 Ensembl:ENSG00000011143 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58218681..58218773 26863196 MeRIP-seq:(Medium) rs756709080 Functional Loss SNV dbSNP153 33..33 33 - - - 97765 RMVar_ID_97765 Human_SNP_ID_628522678 m1A Human chr17 - 58219203 58219203 58219203 CTGTCATGGCGGAGACCGTCTGGAGCACTGACACCGGGGAGGCAGTGTATCGCTCCCGGGACCCC CTGTCATGGCGGAGACCGTCTGGAGCACTGACGCCGGGGAGGCAGTGTATCGCTCCCGGGACCCC T C MKS1 Ensembl:ENSG00000011143 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:58219116..58219210;chr17:58219085..58219212 26863196 MeRIP-seq:(Medium) rs1021790535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237462,Human_RBP_ID_4465572,Human_RBP_ID_13094407 Human_Splice_Rec_1844835,Human_Splice_Rec_1844869,Human_Splice_Rec_1844933,Human_Splice_Rec_1845011,Human_Splice_Rec_1845027,Human_Splice_Rec_1845039,Human_Splice_Rec_1845049 97766 RMVar_ID_97766 Human_SNP_ID_628549221 m1A Human chr17 + 58322770 58322770 58322770 CAGGAGCTGGCCCCTCAGCTCCGCATTCTCCCACTCCACCTGGCGAGGGGGCAGTGACAGGGAGT CAGGAGCTGGCCCCTCAGCTCCGCATTCTCCCCCTCCACCTGGCGAGGGGGCAGTGACAGGGAGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:58322677..58322823 26863196 MeRIP-seq:(Medium) rs750080886 Functional Loss SNV dbSNP153 33..33 33 - - - 97767 RMVar_ID_97767 Human_SNP_ID_628549222 m1A Human chr17 + 58322770 58322770 58322770 CAGGAGCTGGCCCCTCAGCTCCGCATTCTCCCACTCCACCTGGCGAGGGGGCAGTGACAGGGAGT CAGGAGCTGGCCCCTCAGCTCCGCATTCTCCCGCTCCACCTGGCGAGGGGGCAGTGACAGGGAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:58322677..58322823 26863196 MeRIP-seq:(Medium) rs750080886 Functional Loss SNV dbSNP153 33..33 33 - - - 97768 RMVar_ID_97768 Human_SNP_ID_628549226 m1A Human chr17 - 58322778 58322778 58322778 CCCACCCAACTCCCTGTCACTGCCCCCTCGCCAGGTGGAGTGGGAGAATGCGGAGCTGAGGGGCC CCCACCCAACTCCCTGTCACTGCCCCCTCGCCGGGTGGAGTGGGAGAATGCGGAGCTGAGGGGCC T C TSPOAP1 Ensembl:ENSG00000005379 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58322671..58322801 26863196 MeRIP-seq:(Medium) rs1223583873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95047,RMVar_hsa_circ_185636,RMVar_hsa_circ_109829,RMVar_hsa_circ_185637 97769 RMVar_ID_97769 Human_SNP_ID_628592856 m1A Human chr17 + 58512475 58512475 58512475 TGAGGGCATCGGCTGCCCGGCCCAGGAACTCTACTCCCTCACCCTGCAGCACTGTGAAGGGGACC TGAGGGCATCGGCTGCCCGGCCCAGGAACTCTGCTCCCTCACCCTGCAGCACTGTGAAGGGGACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58512426..58512475 32194978 MeRIP-seq:(Medium) rs1212160390 Functional Loss SNV dbSNP153 33..33 33 - - - 97770 RMVar_ID_97770 Human_SNP_ID_628622583 m1A Human chr17 + 58631745 58631720 58631745 AACACTGCTATCCCACTCGTGAGAGAACACAAATATCTCCCTCTCGCGGTTTCCAGCGTTCTACA AACACTGC_________________________TATCTCCCTCTCGCGGTTTCCAGCGTTCTACA CTATCCCACTCGTGAGAGAACACAAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58631695..58631760 26863196 MeRIP-seq:(Medium) rs1301036064 Functional Loss DEL dbSNP153 9..33 33 - - - 97771 RMVar_ID_97771 Human_SNP_ID_628622629 m1A Human chr17 + 58631745 58631742 58631746 AACACTGCTATCCCACTCGTGAGAGAACACAAATATCTCCCTCTCGCGGTTTCCAGCGTTCTACA AACACTGCTATCCCACTCGTGAGAGAACAC____ATCTCCCTCTCGCGGTTTCCAGCGTTCTACA CAAAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58631695..58631760 26863196 MeRIP-seq:(Medium) rs35448751 Functional Loss DEL dbSNP153 31..34 33 - - - 97772 RMVar_ID_97772 Human_SNP_ID_628622637 m1A Human chr17 + 58631745 58631745 58631745 AACACTGCTATCCCACTCGTGAGAGAACACAAATATCTCCCTCTCGCGGTTTCCAGCGTTCTACA AACACTGCTATCCCACTCGTGAGAGAACACAAGTATCTCCCTCTCGCGGTTTCCAGCGTTCTACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58631695..58631760 26863196 MeRIP-seq:(Medium) rs767252500 Functional Loss SNV dbSNP153 33..33 33 - - - 97773 RMVar_ID_97773 Human_SNP_ID_628629926 m1A Human chr17 + 58659168 58659168 58659168 AGTTCAATCACAGGACAGAAAAGCGCAAAAGCAGTCCCCCACTACCACAAGTTATGCAGCCGAGT AGTTCAATCACAGGACAGAAAAGCGCAAAAGCCGTCCCCCACTACCACAAGTTATGCAGCCGAGT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:58659117..58659276 26863196 MeRIP-seq:(Medium) rs933989508 Functional Loss SNV dbSNP153 33..33 33 - - - 97774 RMVar_ID_97774 Human_SNP_ID_628629953 m1A Human chr17 + 58659193 58659193 58659193 CAAAAGCAGTCCCCCACTACCACAAGTTATGCAGCCGAGTTTTCTCATTCGGGGAAATCGCGGGA CAAAAGCAGTCCCCCACTACCACAAGTTATGCTGCCGAGTTTTCTCATTCGGGGAAATCGCGGGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:58659143..58659273 26863196 MeRIP-seq:(Medium) rs1389250168 Functional Loss SNV dbSNP153 33..33 33 - - - 97775 RMVar_ID_97775 Human_SNP_ID_628630039 m1A Human chr17 + 58659243 58659243 58659243 GGGGAAATCGCGGGAGCAAACACATAGTAAAAACCCTCCCCCAAGAAAAACACTTTATCAGGACC GGGGAAATCGCGGGAGCAAACACATAGTAAAACCCCTCCCCCAAGAAAAACACTTTATCAGGACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:58659125..58659273;chr17:58659172..58659279 26863196 MeRIP-seq:(Medium) rs985414167 Functional Loss SNV dbSNP153 33..33 33 - - - 97776 RMVar_ID_97776 Human_SNP_ID_628630040 m1A Human chr17 + 58659243 58659243 58659243 GGGGAAATCGCGGGAGCAAACACATAGTAAAAACCCTCCCCCAAGAAAAACACTTTATCAGGACC GGGGAAATCGCGGGAGCAAACACATAGTAAAAGCCCTCCCCCAAGAAAAACACTTTATCAGGACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:58659125..58659273;chr17:58659172..58659279 26863196 MeRIP-seq:(Medium) rs985414167 Functional Loss SNV dbSNP153 33..33 33 - - - 97777 RMVar_ID_97777 Human_SNP_ID_628630044 m1A Human chr17 - 58659247 58659247 58659247 TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGAGGGTTTTTACTATGTGTTTGCTCCCGCGATTT TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGTGGGTTTTTACTATGTGTTTGCTCCCGCGATTT T A TEX14 Ensembl:ENSG00000121101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:58659131..58659281 26863196 MeRIP-seq:(Medium) rs1008456276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864171,Human_RBP_ID_2515830,Human_RBP_ID_3530263,Human_RBP_ID_4467756,Human_RBP_ID_6620692,Human_RBP_ID_9341063,Human_RBP_ID_13236354,Human_RBP_ID_17126708,Human_RBP_ID_17380487,Human_RBP_ID_17567268,Human_RBP_ID_17582784,Human_RBP_ID_18163960,Human_RBP_ID_18419676,Human_RBP_ID_18486622,Human_RBP_ID_18544461,Human_RBP_ID_22218160,Human_RBP_ID_22960062,Human_RBP_ID_23276747,Human_RBP_ID_23738713,Human_RBP_ID_24371521,Human_RBP_ID_26783110 97778 RMVar_ID_97778 Human_SNP_ID_628630045 m1A Human chr17 - 58659247 58659247 58659247 TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGAGGGTTTTTACTATGTGTTTGCTCCCGCGATTT TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGGGGGTTTTTACTATGTGTTTGCTCCCGCGATTT T C TEX14 Ensembl:ENSG00000121101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:58659131..58659281 26863196 MeRIP-seq:(Medium) rs1008456276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864171,Human_RBP_ID_2515830,Human_RBP_ID_3530263,Human_RBP_ID_4467756,Human_RBP_ID_6620692,Human_RBP_ID_9341063,Human_RBP_ID_13236354,Human_RBP_ID_17126708,Human_RBP_ID_17380487,Human_RBP_ID_17567268,Human_RBP_ID_17582784,Human_RBP_ID_18163960,Human_RBP_ID_18419676,Human_RBP_ID_18486622,Human_RBP_ID_18544461,Human_RBP_ID_22218160,Human_RBP_ID_22960062,Human_RBP_ID_23276747,Human_RBP_ID_23738713,Human_RBP_ID_24371521,Human_RBP_ID_26783110 97779 RMVar_ID_97779 Human_SNP_ID_628630046 m1A Human chr17 - 58659247 58659247 58659247 TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGAGGGTTTTTACTATGTGTTTGCTCCCGCGATTT TGTTGGTCCTGATAAAGTGTTTTTCTTGGGGGCGGGTTTTTACTATGTGTTTGCTCCCGCGATTT T G TEX14 Ensembl:ENSG00000121101 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:58659131..58659281 26863196 MeRIP-seq:(Medium) rs1008456276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864171,Human_RBP_ID_2515830,Human_RBP_ID_3530263,Human_RBP_ID_4467756,Human_RBP_ID_6620692,Human_RBP_ID_9341063,Human_RBP_ID_13236354,Human_RBP_ID_17126708,Human_RBP_ID_17380487,Human_RBP_ID_17567268,Human_RBP_ID_17582784,Human_RBP_ID_18163960,Human_RBP_ID_18419676,Human_RBP_ID_18486622,Human_RBP_ID_18544461,Human_RBP_ID_22218160,Human_RBP_ID_22960062,Human_RBP_ID_23276747,Human_RBP_ID_23738713,Human_RBP_ID_24371521,Human_RBP_ID_26783110 97780 RMVar_ID_97780 Human_SNP_ID_628635479 m1A Human chr17 - 58679613 58679613 58679613 TTTCAGGGTGAGGTTTGTCTCTTGCATTGTGGATGTGCTGACCCCTGTGGTTTTCTACAAATGTG TTTCAGGGTGAGGTTTGTCTCTTGCATTGTGGTTGTGCTGACCCCTGTGGTTTTCTACAAATGTG T A AC011195.3,RNVU1-34,TEX14 Ensembl:ENSG00000266826,Ensembl:ENSG00000200997,Ensembl:ENSG00000121101 Protein coding,snRNA,Protein coding intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58679562..58679636 26863196 MeRIP-seq:(Medium) rs1234864456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864174,Human_RBP_ID_2515845,Human_RBP_ID_3530269,Human_RBP_ID_4467755,Human_RBP_ID_5189011,Human_RBP_ID_5248376,Human_RBP_ID_6620706,Human_RBP_ID_8458356,Human_RBP_ID_8824860,Human_RBP_ID_9327387,Human_RBP_ID_9424670,Human_RBP_ID_13094950,Human_RBP_ID_17380415,Human_RBP_ID_17495400,Human_RBP_ID_17609830,Human_RBP_ID_17673502,Human_RBP_ID_17906036,Human_RBP_ID_18488134,Human_RBP_ID_18531720,Human_RBP_ID_19087071,Human_RBP_ID_21976771,Human_RBP_ID_22358454,Human_RBP_ID_22531561,Human_RBP_ID_22762293,Human_RBP_ID_23110419,Human_RBP_ID_23738718,Human_RBP_ID_24415661,Human_RBP_ID_24532356,Human_RBP_ID_24552569,Human_RBP_ID_26453815,Human_RBP_ID_26783103,Human_RBP_ID_26967419,Human_RBP_ID_27572952 Human_miRNA_ID_3128471 97781 RMVar_ID_97781 Human_SNP_ID_628635480 m1A Human chr17 - 58679613 58679613 58679613 TTTCAGGGTGAGGTTTGTCTCTTGCATTGTGGATGTGCTGACCCCTGTGGTTTTCTACAAATGTG TTTCAGGGTGAGGTTTGTCTCTTGCATTGTGGGTGTGCTGACCCCTGTGGTTTTCTACAAATGTG T C AC011195.3,RNVU1-34,TEX14 Ensembl:ENSG00000266826,Ensembl:ENSG00000200997,Ensembl:ENSG00000121101 Protein coding,snRNA,Protein coding intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58679562..58679636 26863196 MeRIP-seq:(Medium) rs1234864456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864174,Human_RBP_ID_2515845,Human_RBP_ID_3530269,Human_RBP_ID_4467755,Human_RBP_ID_5189011,Human_RBP_ID_5248376,Human_RBP_ID_6620706,Human_RBP_ID_8458356,Human_RBP_ID_8824860,Human_RBP_ID_9327387,Human_RBP_ID_9424670,Human_RBP_ID_13094950,Human_RBP_ID_17380415,Human_RBP_ID_17495400,Human_RBP_ID_17609830,Human_RBP_ID_17673502,Human_RBP_ID_17906036,Human_RBP_ID_18488134,Human_RBP_ID_18531720,Human_RBP_ID_19087071,Human_RBP_ID_21976771,Human_RBP_ID_22358454,Human_RBP_ID_22531561,Human_RBP_ID_22762293,Human_RBP_ID_23110419,Human_RBP_ID_23738718,Human_RBP_ID_24415661,Human_RBP_ID_24532356,Human_RBP_ID_24552569,Human_RBP_ID_26453815,Human_RBP_ID_26783103,Human_RBP_ID_26967419,Human_RBP_ID_27572952 Human_miRNA_ID_3128471 97782 RMVar_ID_97782 Human_SNP_ID_628635498 m1A Human chr17 - 58679635 58679635 58679635 ACATGATCATTAAAGGTGGATTTTTCAGGGTGAGGTTTGTCTCTTGCATTGTGGATGTGCTGACC ACATGATCATTAAAGGTGGATTTTTCAGGGTGGGGTTTGTCTCTTGCATTGTGGATGTGCTGACC T C AC011195.3,RNVU1-34,TEX14 Ensembl:ENSG00000266826,Ensembl:ENSG00000200997,Ensembl:ENSG00000121101 Protein coding,snRNA,Protein coding intron,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58679562..58679637 26863196 MeRIP-seq:(Medium) rs185326554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1132058,Human_RBP_ID_1538408,Human_RBP_ID_1864177,Human_RBP_ID_2515845,Human_RBP_ID_3530269,Human_RBP_ID_4467755,Human_RBP_ID_5248376,Human_RBP_ID_5260670,Human_RBP_ID_6620707,Human_RBP_ID_8255347,Human_RBP_ID_8458357,Human_RBP_ID_8824860,Human_RBP_ID_9327387,Human_RBP_ID_13094950,Human_RBP_ID_17081247,Human_RBP_ID_17609830,Human_RBP_ID_17673502,Human_RBP_ID_17693538,Human_RBP_ID_17906036,Human_RBP_ID_18703924,Human_RBP_ID_19087071,Human_RBP_ID_21976771,Human_RBP_ID_22741157,Human_RBP_ID_22762293,Human_RBP_ID_23114540,Human_RBP_ID_23276758,Human_RBP_ID_23738719,Human_RBP_ID_24415662,Human_RBP_ID_24480111,Human_RBP_ID_24532356,Human_RBP_ID_24552569,Human_RBP_ID_26644099,Human_RBP_ID_27796918 97783 RMVar_ID_97783 Human_SNP_ID_628639126 m1A Human chr17 - 58692672 58692672 58692672 GAGACAGCGGGAAACTCACCAAATCCCGCTGCATTTCAAAGCGGAACGTCTTCCCGCGCATCGCA GAGACAGCGGGAAACTCACCAAATCCCGCTGCGTTTCAAAGCGGAACGTCTTCCCGCGCATCGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58692622..58692750 26863196 MeRIP-seq:(Medium) rs730881936 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_594 97784 RMVar_ID_97784 Human_SNP_ID_628639127 m1A Human chr17 - 58692672 58692672 58692672 GAGACAGCGGGAAACTCACCAAATCCCGCTGCATTTCAAAGCGGAACGTCTTCCCGCGCATCGCA GAGACAGCGGGAAACTCACCAAATCCCGCTGCCTTTCAAAGCGGAACGTCTTCCCGCGCATCGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58692622..58692750 26863196 MeRIP-seq:(Medium) rs730881936 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_594 97785 RMVar_ID_97785 Human_SNP_ID_628639131 m1A Human chr17 + 58692675 58692675 58692675 GATGCGCGGGAAGACGTTCCGCTTTGAAATGCAGCGGGATTTGGTGAGTTTCCCGCTGTCTCCAG GATGCGCGGGAAGACGTTCCGCTTTGAAATGCCGCGGGATTTGGTGAGTTTCCCGCTGTCTCCAG A C RAD51C Ensembl:ENSG00000108384 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58692626..58692727 26863196 MeRIP-seq:(Medium) rs730881937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4441754,Human_RBP_ID_23210056,Human_RBP_ID_23738722 Human_Splice_Rec_1846519 Clinvar_Rec_595 97786 RMVar_ID_97786 Human_SNP_ID_628639132 m1A Human chr17 + 58692675 58692675 58692675 GATGCGCGGGAAGACGTTCCGCTTTGAAATGCAGCGGGATTTGGTGAGTTTCCCGCTGTCTCCAG GATGCGCGGGAAGACGTTCCGCTTTGAAATGCGGCGGGATTTGGTGAGTTTCCCGCTGTCTCCAG A G RAD51C Ensembl:ENSG00000108384 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58692626..58692727 26863196 MeRIP-seq:(Medium) rs730881937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4441754,Human_RBP_ID_23210056,Human_RBP_ID_23738722 Human_Splice_Rec_1846519 Clinvar_Rec_595 97787 RMVar_ID_97787 Human_SNP_ID_628639144 m1A Human chr17 + 58692689 58692689 58692689 CGTTCCGCTTTGAAATGCAGCGGGATTTGGTGAGTTTCCCGCTGTCTCCAGCGGTGCGGGTGAAG CGTTCCGCTTTGAAATGCAGCGGGATTTGGTGGGTTTCCCGCTGTCTCCAGCGGTGCGGGTGAAG A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:58692638..58692733 26863196 MeRIP-seq:(Medium) rs762060755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495513,Human_RBP_ID_4441754,Human_RBP_ID_23210056,Human_RBP_ID_23738722 Human_Splice_Rec_1846527,Human_Splice_Rec_1846549,Human_Splice_Rec_1846565,Human_Splice_Rec_1846583,Human_Splice_Rec_1846597,Human_Splice_Rec_1846611,Human_Splice_Rec_1846613 97788 RMVar_ID_97788 Human_SNP_ID_628639217 m1A Human chr17 + 58692769 58692769 58692769 TTCCAGACTGCTGAGGAACTCCTAGAGGTGAAACCCTCCGAGCTTAGCAAAGGTAACGACTCCTG TTCCAGACTGCTGAGGAACTCCTAGAGGTGAAGCCCTCCGAGCTTAGCAAAGGTAACGACTCCTG A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58692718..58692843 32194978 MeRIP-seq:(Medium) rs1278628494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1009564,Human_RBP_ID_1538411,Human_RBP_ID_1864179,Human_RBP_ID_3530272,Human_RBP_ID_4465580,Human_RBP_ID_6620710,Human_RBP_ID_8941912,Human_RBP_ID_13094958,Human_RBP_ID_18991907,Human_RBP_ID_19083348,Human_RBP_ID_23210056 Human_Splice_Rec_1846527,Human_Splice_Rec_1846549,Human_Splice_Rec_1846565,Human_Splice_Rec_1846583,Human_Splice_Rec_1846597,Human_Splice_Rec_1846611,Human_Splice_Rec_1846613 97789 RMVar_ID_97789 Human_SNP_ID_628639255 m1A Human chr17 + 58692817 58692817 58692817 AAAGGTAACGACTCCTGATGGCAAGCTGAGGCACACCGGCCGCCGTCAGCGCCGCCTCAGTCTTC AAAGGTAACGACTCCTGATGGCAAGCTGAGGCTCACCGGCCGCCGTCAGCGCCGCCTCAGTCTTC A T RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58692814..58692879 26863196 MeRIP-seq:(Medium) rs768612583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6620711,Human_RBP_ID_19083348 97790 RMVar_ID_97790 Human_SNP_ID_628703230 m1A Human chr17 + 58965704 58965704 58965704 GGTTTCTGTGTTTCTTTCACAGAGATTGAGACAGTGAAATTGGCCCGTTCTGTCTTCAGCAAACT GGTTTCTGTGTTTCTTTCACAGAGATTGAGACGGTGAAATTGGCCCGTTCTGTCTTCAGCAAACT A G PPM1E Ensembl:ENSG00000175175 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:58965702..58965789 26863410 MeRIP-seq:(Medium) rs1165599687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1846674 RMVar_hsa_circ_39735,RMVar_hsa_circ_306525,RMVar_hsa_circ_338030,RMVar_hsa_circ_284368,RMVar_hsa_circ_185675,RMVar_hsa_circ_185676,RMVar_hsa_circ_185677,RMVar_hsa_circ_185679,RMVar_hsa_circ_185674,RMVar_hsa_circ_322334,RMVar_hsa_circ_185678 97791 RMVar_ID_97791 Human_SNP_ID_628718201 m1A Human chr17 + 59027939 59027939 59027939 ACTTTGCAGTTTCTGTTCTGTTTACCCAGAACACTGCTTGCCCTAGATCTATAAATAGCTGCCAC ACTTTGCAGTTTCTGTTCTGTTTACCCAGAACGCTGCTTGCCCTAGATCTATAAATAGCTGCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:59027817..59028087 26863196 MeRIP-seq:(Medium) rs906575012 Functional Loss SNV dbSNP153 33..33 33 - - - 97792 RMVar_ID_97792 Human_SNP_ID_628718217 m1A Human chr17 + 59028039 59028039 59028039 TCCTCACAGAGACTTTCTCTGACTACCCCAATAGAACATGTCTCATCTGCTCCTCCCATCCCACT TCCTCACAGAGACTTTCTCTGACTACCCCAATGGAACATGTCTCATCTGCTCCTCCCATCCCACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:59027848..59028060 26863196 MeRIP-seq:(Medium) rs1286235859 Functional Loss SNV dbSNP153 33..33 33 - - - 97793 RMVar_ID_97793 Human_SNP_ID_628731524 m1A Human chr17 - 59079820 59079820 59079820 ATGCAAAAGATGAGCGTGTTCGGGAAATTAGGAATGCAGTGGAGATGATGATTGCACGGTTAGAC ATGCAAAAGATGAGCGTGTTCGGGAAATTAGGCATGCAGTGGAGATGATGATTGCACGGTTAGAC T G TRIM37 Ensembl:ENSG00000108395 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:59079771..59079872 26863196 MeRIP-seq:(Medium) rs766059485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864491,Human_RBP_ID_5577588,Human_RBP_ID_13099926,Human_RBP_ID_23739125 Human_Splice_Rec_1846708,Human_Splice_Rec_1846709,Human_Splice_Rec_1846758,Human_Splice_Rec_1846759,Human_Splice_Rec_1846802,Human_Splice_Rec_1846803,Human_Splice_Rec_1846846,Human_Splice_Rec_1846847,Human_Splice_Rec_1846882,Human_Splice_Rec_1846883,Human_Splice_Rec_1846895,Human_Splice_Rec_1846906,Human_Splice_Rec_1846907,Human_Splice_Rec_1846918 Human_miRNA_ID_1540679,Human_miRNA_ID_1594352,Human_miRNA_ID_2235385,Human_miRNA_ID_2969627,Human_miRNA_ID_3029549 RMVar_hsa_circ_313386,RMVar_hsa_circ_2033,RMVar_hsa_circ_185682,RMVar_hsa_circ_33718,RMVar_hsa_circ_284542,RMVar_hsa_circ_375375,RMVar_hsa_circ_98405,RMVar_hsa_circ_185696,RMVar_hsa_circ_185698,RMVar_hsa_circ_185699,RMVar_hsa_circ_185697,RMVar_hsa_circ_106105,RMVar_hsa_circ_185709,RMVar_hsa_circ_185703,RMVar_hsa_circ_371211,RMVar_hsa_circ_335074,RMVar_hsa_circ_350749,RMVar_hsa_circ_185708,RMVar_hsa_circ_278743,RMVar_hsa_circ_185710,RMVar_hsa_circ_331248,RMVar_hsa_circ_185719,RMVar_hsa_circ_376690,RMVar_hsa_circ_52843,RMVar_hsa_circ_185725,RMVar_hsa_circ_185726,RMVar_hsa_circ_349656,RMVar_hsa_circ_376507,RMVar_hsa_circ_303374,RMVar_hsa_circ_284967,RMVar_hsa_circ_25861,RMVar_hsa_circ_36607,RMVar_hsa_circ_103840,RMVar_hsa_circ_185727,RMVar_hsa_circ_185728,RMVar_hsa_circ_315596,RMVar_hsa_circ_310430,RMVar_hsa_circ_288790,RMVar_hsa_circ_185734,RMVar_hsa_circ_291329,RMVar_hsa_circ_313544,RMVar_hsa_circ_185735,RMVar_hsa_circ_287279,RMVar_hsa_circ_41403,RMVar_hsa_circ_41589,RMVar_hsa_circ_185739,RMVar_hsa_circ_185740,RMVar_hsa_circ_185738,RMVar_hsa_circ_301787,RMVar_hsa_circ_323884,RMVar_hsa_circ_314935,RMVar_hsa_circ_288278,RMVar_hsa_circ_17756,RMVar_hsa_circ_185741,RMVar_hsa_circ_185743,RMVar_hsa_circ_185744,RMVar_hsa_circ_185742,RMVar_hsa_circ_289353,RMVar_hsa_circ_22630,RMVar_hsa_circ_348968,RMVar_hsa_circ_349303,RMVar_hsa_circ_73368,RMVar_hsa_circ_314749,RMVar_hsa_circ_325782,RMVar_hsa_circ_341307,RMVar_hsa_circ_316664,RMVar_hsa_circ_293644,RMVar_hsa_circ_185747,RMVar_hsa_circ_185748,RMVar_hsa_circ_276846,RMVar_hsa_circ_337675,RMVar_hsa_circ_265955,RMVar_hsa_circ_185749,RMVar_hsa_circ_185750 97794 RMVar_ID_97794 Human_SNP_ID_628731531 m1A Human chr17 + 59079833 59079833 59079833 ATCATCATCTCCACTGCATTCCTAATTTCCCGAACACGCTCATCTTTTGCATTTCTTACAGCTTC ATCATCATCTCCACTGCATTCCTAATTTCCCGCACACGCTCATCTTTTGCATTTCTTACAGCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:59079751..59079900 26863196 MeRIP-seq:(Medium) rs756702082 Functional Loss SNV dbSNP153 33..33 33 - - - 97795 RMVar_ID_97795 Human_SNP_ID_628738819 m1A Human chr17 - 59107133 59107133 59107133 CGGGTGTGGCTCTGAAGTCTGCGCTTTCCACCAGTACGCCAGGTGGCTCCGTCTTTGGCGCGCAA CGGGTGTGGCTCTGAAGTCTGCGCTTTCCACCGGTACGCCAGGTGGCTCCGTCTTTGGCGCGCAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:59107043..59107192 26863196 MeRIP-seq:(Medium) rs1406471113 Functional Loss SNV dbSNP153 33..33 33 - - - 97796 RMVar_ID_97796 Human_SNP_ID_628749907 m1A Human chr17 - 59154504 59154504 59154504 AAGGGGATCGTAACCACGAGCTCCGCTCCCGGAGCGCGGGCGGGATTGAGACAGGAAAGGCATCC AAGGGGATCGTAACCACGAGCTCCGCTCCCGGGGCGCGGGCGGGATTGAGACAGGAAAGGCATCC T C SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:59154497..59154598 26863196 MeRIP-seq:(Medium) rs181195207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5185938,Human_RBP_ID_5319190,Human_RBP_ID_9327388 97797 RMVar_ID_97797 Human_SNP_ID_628755528 m1A Human chr17 + 59177208 59177208 59177208 GGAATAAATGAATGCATTGGTATTGCCGGGAGAAGAGGCCGGCGCGGCTAAAATATGCTATGACC GGAATAAATGAATGCATTGGTATTGCCGGGAGGAGAGGCCGGCGCGGCTAAAATATGCTATGACC A G PRR11 Ensembl:ENSG00000068489 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:59177202..59177447 26863196 MeRIP-seq:(Medium) rs534733704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335578,RMVar_hsa_circ_185759 97798 RMVar_ID_97798 Human_SNP_ID_628763525 m1A Human chr17 - 59210104 59210104 59210104 CAGTAGGGGACCCTCCGGGACTTTCAGAGCCCATCCAGGCTGATGCTCCCATTAGAAGGTCTCGC CAGTAGGGGACCCTCCGGGACTTTCAGAGCCCTTCCAGGCTGATGCTCCCATTAGAAGGTCTCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:59210053..59210181;chr17:59210056..59210203;chr17:59210053..59210193 26863196 MeRIP-seq:(Medium) rs779748114 Functional Loss SNV dbSNP153 33..33 33 - - - 97799 RMVar_ID_97799 Human_SNP_ID_628779776 m1A Human chr17 + 59274657 59274657 59274657 AAAAATTAGCTGGGCGTGGTGGTGGGCACCTTAGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA AAAAATTAGCTGGGCGTGGTGGTGGGCACCTTTGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA A T GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1452096015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 97800 RMVar_ID_97800 Human_SNP_ID_628860819 m1A Human chr17 + 59605640 59605640 59605640 CGACGTGAAGTGAGAGAAGATGCAAGAAGGAGATGGACAAATAAGGAAAATGTAAAGCAGCTAAA CGACGTGAAGTGAGAGAAGATGCAAGAAGGAGGTGGACAAATAAGGAAAATGTAAAGCAGCTAAA A G DHX40 Ensembl:ENSG00000108406 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59605589..59607048 32194978 MeRIP-seq:(Medium) rs879331825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864647,Human_RBP_ID_6623149 Human_Splice_Rec_1847369,Human_Splice_Rec_1847409,Human_Splice_Rec_1847449 RMVar_hsa_circ_114130,RMVar_hsa_circ_42717,RMVar_hsa_circ_185786,RMVar_hsa_circ_339221,RMVar_hsa_circ_8299,RMVar_hsa_circ_29902,RMVar_hsa_circ_185790 97801 RMVar_ID_97801 Human_SNP_ID_628860820 m1A Human chr17 + 59605640 59605640 59605640 CGACGTGAAGTGAGAGAAGATGCAAGAAGGAGATGGACAAATAAGGAAAATGTAAAGCAGCTAAA CGACGTGAAGTGAGAGAAGATGCAAGAAGGAGTTGGACAAATAAGGAAAATGTAAAGCAGCTAAA A T DHX40 Ensembl:ENSG00000108406 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59605589..59607048 32194978 MeRIP-seq:(Medium) rs879331825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864647,Human_RBP_ID_6623149 Human_Splice_Rec_1847369,Human_Splice_Rec_1847409,Human_Splice_Rec_1847449 RMVar_hsa_circ_114130,RMVar_hsa_circ_42717,RMVar_hsa_circ_185786,RMVar_hsa_circ_339221,RMVar_hsa_circ_8299,RMVar_hsa_circ_29902,RMVar_hsa_circ_185790 97802 RMVar_ID_97802 Human_SNP_ID_628864376 m1A Human chr17 - 59619796 59619796 59619796 CCCCTCCACGGAGCGCCGCGCGCGGCGGGCGCAGGAATTCGGGGCGCAGTGCGCCCGGTGCCTCG CCCCTCCACGGAGCGCCGCGCGCGGCGGGCGCGGGAATTCGGGGCGCAGTGCGCCCGGTGCCTCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:59619746..59619839 26863196 MeRIP-seq:(Medium) rs1471323914 Functional Loss SNV dbSNP153 33..33 33 - - - 97803 RMVar_ID_97803 Human_SNP_ID_628864462 m1A Human chr17 - 59619959 59619959 59619959 CAGGCAGACGAAAGAGCTCGGGTCGGGGGCGGAGGCTCCAGGGGCCAGGAGAGCCGCAATGGCGG CAGGCAGACGAAAGAGCTCGGGTCGGGGGCGGGGGCTCCAGGGGCCAGGAGAGCCGCAATGGCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:59619900..59620150 26863196 MeRIP-seq:(Medium) rs980520981 Functional Loss SNV dbSNP153 33..33 33 - - - 97804 RMVar_ID_97804 Human_SNP_ID_628864463 m1A Human chr17 - 59619959 59619959 59619959 CAGGCAGACGAAAGAGCTCGGGTCGGGGGCGGAGGCTCCAGGGGCCAGGAGAGCCGCAATGGCGG CAGGCAGACGAAAGAGCTCGGGTCGGGGGCGGCGGCTCCAGGGGCCAGGAGAGCCGCAATGGCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:59619900..59620150 26863196 MeRIP-seq:(Medium) rs980520981 Functional Loss SNV dbSNP153 33..33 33 - - - 97805 RMVar_ID_97805 Human_SNP_ID_628864477 m1A Human chr17 + 59619994 59619994 59619994 GCCCCCGACCCGAGCTCTTTCGTCTGCCTGCCAGTTTCCTGCGTCCCCGGAGAGGATCCTGCTGA GCCCCCGACCCGAGCTCTTTCGTCTGCCTGCCGGTTTCCTGCGTCCCCGGAGAGGATCCTGCTGA A G CLTC Ensembl:ENSG00000141367 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr17:59619876..59620175;chr17:59619876..59620150 26863410,26863196 MeRIP-seq:(Medium) rs1233956391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50662,Human_RBP_ID_133551,Human_RBP_ID_495927,Human_RBP_ID_1538667,Human_RBP_ID_4442308,Human_RBP_ID_5441698,Human_RBP_ID_8820525,Human_RBP_ID_9257894,Human_RBP_ID_9289253,Human_RBP_ID_13101980,Human_RBP_ID_17378474,Human_RBP_ID_18943447,Human_RBP_ID_20245859,Human_RBP_ID_22218318,Human_RBP_ID_23739533,Human_RBP_ID_27257633 97806 RMVar_ID_97806 Human_SNP_ID_628864524 m1A Human chr17 + 59620116 59620116 59620116 GCCCCGCAGCCCCAGTGACAGGAGGAGACCATAACCCCCGACAGCGCCATGGCCCAGATTCTGCC GCCCCGCAGCCCCAGTGACAGGAGGAGACCATTACCCCCGACAGCGCCATGGCCCAGATTCTGCC A T CLTC Ensembl:ENSG00000141367 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:59619851..59644375 26863196 MeRIP-seq:(Medium) rs991829612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50662,Human_RBP_ID_495929,Human_RBP_ID_4442313,Human_RBP_ID_5441701,Human_RBP_ID_5466762,Human_RBP_ID_5497467,Human_RBP_ID_8458670,Human_RBP_ID_9074404,Human_RBP_ID_9289258,Human_RBP_ID_17378477,Human_RBP_ID_18704249,Human_RBP_ID_18943447 Human_Splice_Rec_1847451,Human_Splice_Rec_1847513,Human_Splice_Rec_1847573,Human_Splice_Rec_1847635,Human_Splice_Rec_1847639,Human_Splice_Rec_1847663 Human_miRNA_ID_1806458 97807 RMVar_ID_97807 Human_SNP_ID_628875215 m1A Human chr17 + 59666575 59666575 59666575 CTGTGTGAAAAGGCTGGCCTACTGCAGCGTGCATTAGAACATTTCACTGATTTATATGATATAAA CTGTGTGAAAAGGCTGGCCTACTGCAGCGTGCGTTAGAACATTTCACTGATTTATATGATATAAA A G CLTC Ensembl:ENSG00000141367 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59666211..59666601 32194978 MeRIP-seq:(Medium) rs745528322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495949,Human_RBP_ID_1538738,Human_RBP_ID_1864737,Human_RBP_ID_3531122,Human_RBP_ID_6623458,Human_RBP_ID_8820569,Human_RBP_ID_9074436,Human_RBP_ID_9257921,Human_RBP_ID_9289279,Human_RBP_ID_17261195,Human_RBP_ID_17492857,Human_RBP_ID_22443088,Human_RBP_ID_22475394,Human_RBP_ID_22761612 Human_Splice_Rec_1847472,Human_Splice_Rec_1847473,Human_Splice_Rec_1847534,Human_Splice_Rec_1847535,Human_Splice_Rec_1847594,Human_Splice_Rec_1847595,Human_Splice_Rec_1847686,Human_Splice_Rec_1847687 Human_miRNA_ID_1505588,Human_miRNA_ID_1774164,Human_miRNA_ID_2769285,Human_miRNA_ID_2912525 RMVar_hsa_circ_31938,RMVar_hsa_circ_6356,RMVar_hsa_circ_378026,RMVar_hsa_circ_67245,RMVar_hsa_circ_89013,RMVar_hsa_circ_24294,RMVar_hsa_circ_17451,RMVar_hsa_circ_185795,RMVar_hsa_circ_266388,RMVar_hsa_circ_374301,RMVar_hsa_circ_52794,RMVar_hsa_circ_185796,RMVar_hsa_circ_50730,RMVar_hsa_circ_361315,RMVar_hsa_circ_185798,RMVar_hsa_circ_24250,RMVar_hsa_circ_33496,RMVar_hsa_circ_60555,RMVar_hsa_circ_369665,RMVar_hsa_circ_57273,RMVar_hsa_circ_80053,RMVar_hsa_circ_97121,RMVar_hsa_circ_185801,RMVar_hsa_circ_185802,RMVar_hsa_circ_367221,RMVar_hsa_circ_87121,RMVar_hsa_circ_185804,RMVar_hsa_circ_5046,RMVar_hsa_circ_185805,RMVar_hsa_circ_185803,RMVar_hsa_circ_9572,RMVar_hsa_circ_38448,RMVar_hsa_circ_103547,RMVar_hsa_circ_27449,RMVar_hsa_circ_316621,RMVar_hsa_circ_64707,RMVar_hsa_circ_185806,RMVar_hsa_circ_185807,RMVar_hsa_circ_52779,RMVar_hsa_circ_8756,RMVar_hsa_circ_23382 97808 RMVar_ID_97808 Human_SNP_ID_628875643 m1A Human chr17 - 59668862 59668862 59668862 CTACAGATTCTTTCTACTTCTTTGATTTGCCCAGTCTTGCAAGCTGCCTGAATATATTTAAAGTG CTACAGATTCTTTCTACTTCTTTGATTTGCCCGGTCTTGCAAGCTGCCTGAATATATTTAAAGTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59667052..59668863 32194978 MeRIP-seq:(Medium) rs1374732860 Functional Loss SNV dbSNP153 33..33 33 - - - 97809 RMVar_ID_97809 Human_SNP_ID_628881247 m1A Human chr17 + 59694073 59694073 59694073 TTTAGAATTTATTTTCGAAGGGGAATAGTTTCAATGTTTTATTCACTTGGGCTTTTTTTCTTCCC TTTAGAATTTATTTTCGAAGGGGAATAGTTTCCATGTTTTATTCACTTGGGCTTTTTTTCTTCCC A C CLTC Ensembl:ENSG00000141367 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59690708..59694259 32194978 MeRIP-seq:(Medium) rs1264257561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864824,Human_RBP_ID_3531185,Human_RBP_ID_6623644,Human_RBP_ID_13103861,Human_RBP_ID_17263070,Human_RBP_ID_17376915,Human_RBP_ID_17492885,Human_RBP_ID_24415695,Human_RBP_ID_27667969 Human_miRNA_ID_853477,Human_miRNA_ID_1715534 RMVar_hsa_circ_103547,RMVar_hsa_circ_185807,RMVar_hsa_circ_185815,RMVar_hsa_circ_89432,RMVar_hsa_circ_96798,RMVar_hsa_circ_185818,RMVar_hsa_circ_113098,RMVar_hsa_circ_185819 97810 RMVar_ID_97810 Human_SNP_ID_628881382 m1A Human chr17 + 59694659 59694659 59694659 TGTGTATGTTGGATATTGTGGTGTTTTAGATCACTGAGTGTACAGAAGAGAGAAATTCAAACAAA TGTGTATGTTGGATATTGTGGTGTTTTAGATCCCTGAGTGTACAGAAGAGAGAAATTCAAACAAA A C CLTC Ensembl:ENSG00000141367 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59694608..59694809 32194978 MeRIP-seq:(Medium) rs1060666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496002,Human_RBP_ID_1287904,Human_RBP_ID_1538858,Human_RBP_ID_1864832,Human_RBP_ID_2516439,Human_RBP_ID_3531192,Human_RBP_ID_5114802,Human_RBP_ID_6623684,Human_RBP_ID_8820696,Human_RBP_ID_13103887,Human_RBP_ID_17492901,Human_RBP_ID_18294857,Human_RBP_ID_18704377,Human_RBP_ID_22389763,Human_RBP_ID_22500075,Human_RBP_ID_23210062,Human_RBP_ID_23739783,Human_RBP_ID_24480217,Human_RBP_ID_26454038,Human_RBP_ID_27667981 RMVar_hsa_circ_103547,RMVar_hsa_circ_185807,RMVar_hsa_circ_185815,RMVar_hsa_circ_89432,RMVar_hsa_circ_96798,RMVar_hsa_circ_185818,RMVar_hsa_circ_113098,RMVar_hsa_circ_185819 97811 RMVar_ID_97811 Human_SNP_ID_628881383 m1A Human chr17 + 59694659 59694659 59694659 TGTGTATGTTGGATATTGTGGTGTTTTAGATCACTGAGTGTACAGAAGAGAGAAATTCAAACAAA TGTGTATGTTGGATATTGTGGTGTTTTAGATCGCTGAGTGTACAGAAGAGAGAAATTCAAACAAA A G CLTC Ensembl:ENSG00000141367 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:59694608..59694809 32194978 MeRIP-seq:(Medium) rs1060666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496002,Human_RBP_ID_1287904,Human_RBP_ID_1538858,Human_RBP_ID_1864832,Human_RBP_ID_2516439,Human_RBP_ID_3531192,Human_RBP_ID_5114802,Human_RBP_ID_6623684,Human_RBP_ID_8820696,Human_RBP_ID_13103887,Human_RBP_ID_17492901,Human_RBP_ID_18294857,Human_RBP_ID_18704377,Human_RBP_ID_22389763,Human_RBP_ID_22500075,Human_RBP_ID_23210062,Human_RBP_ID_23739783,Human_RBP_ID_24480217,Human_RBP_ID_26454038,Human_RBP_ID_27667981 RMVar_hsa_circ_103547,RMVar_hsa_circ_185807,RMVar_hsa_circ_185815,RMVar_hsa_circ_89432,RMVar_hsa_circ_96798,RMVar_hsa_circ_185818,RMVar_hsa_circ_113098,RMVar_hsa_circ_185819 97812 RMVar_ID_97812 Human_SNP_ID_628884175 m1A Human chr17 + 59706301 59706301 59706301 TTCTAATTCCCCTGCCTCAGTAAACCCATTTCAGTAGTGCTCTTGATCCCATTACCTCCTTCTGC TTCTAATTCCCCTGCCTCAGTAAACCCATTTCGGTAGTGCTCTTGATCCCATTACCTCCTTCTGC A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:59706298..59706397 26863196 MeRIP-seq:(Medium) rs1170816820 Functional Loss SNV dbSNP153 33..33 33 - - - 97813 RMVar_ID_97813 Human_SNP_ID_628884454 m1A Human chr17 - 59707328 59707328 59707328 TGGCTCCTTACAGGGCGAAGGAGACCAATATCATTATTCATTTTCTCGCCAGTAGGAACGTTTCT TGGCTCCTTACAGGGCGAAGGAGACCAATATCGTTATTCATTTTCTCGCCAGTAGGAACGTTTCT T C PTRH2 Ensembl:ENSG00000141378 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:59707326..59707399 26863196 MeRIP-seq:(Medium) rs935697607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1864880,Human_RBP_ID_6623788,Human_RBP_ID_8090888,Human_RBP_ID_9078612,Human_RBP_ID_17005779,Human_RBP_ID_17897735,Human_RBP_ID_18419680,Human_RBP_ID_19079624,Human_RBP_ID_23276001,Human_RBP_ID_24415699,Human_RBP_ID_24480226 RMVar_hsa_circ_108115,RMVar_hsa_circ_185822 97814 RMVar_ID_97814 Human_SNP_ID_628884605 m1A Human chr17 + 59707712 59707712 59707712 GCGGGTGTGAGAGTCCGTAAGGAGCAGCTTCCAGGATCCTGAGATCCGGAGCAGCCGGGGTCGGA GCGGGTGTGAGAGTCCGTAAGGAGCAGCTTCCGGGATCCTGAGATCCGGAGCAGCCGGGGTCGGA A G VMP1 Ensembl:ENSG00000062716 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:59707651..59707793;chr17:59707676..59707835 26863196 MeRIP-seq:(Medium) rs908248699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235667,Human_RBP_ID_4464699,Human_RBP_ID_9376496,Human_RBP_ID_18419681,Human_RBP_ID_23739828 Human_Splice_Rec_1847727,Human_Splice_Rec_1847735,Human_Splice_Rec_1847743,Human_Splice_Rec_1847751,Human_Splice_Rec_1847773,Human_Splice_Rec_1847781,Human_Splice_Rec_1847785,Human_Splice_Rec_1847795 RMVar_hsa_circ_185824,RMVar_hsa_circ_107652,RMVar_hsa_circ_111770,RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_185823 97815 RMVar_ID_97815 Human_SNP_ID_628901853 m1A Human chr17 - 59784338 59784336 59784339 CATAAATTGAAAGGTAAGAAAACTGAAAAAGTAGACATGCAGATGGGAAGAAATGACACACTAGG CATAAATTGAAAGGTAAGAAAACTGAAAAAG___ACATGCAGATGGGAAGAAATGACACACTAGG TCTA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:59784327..59784428 26863196 MeRIP-seq:(Medium) rs1454765030 Functional Loss DEL dbSNP153 32..34 33 - - - 97816 RMVar_ID_97816 Human_SNP_ID_628929185 m1A Human chr17 + 59893282 59893282 59893282 GGACATGGCAGGAGTGTTTGACATAGACCTGGACCAGCCAGAGGACGCGGGCTCTGAGGATGAGC GGACATGGCAGGAGTGTTTGACATAGACCTGGCCCAGCCAGAGGACGCGGGCTCTGAGGATGAGC A C RPS6KB1 Ensembl:ENSG00000108443 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:59893126..59893815 26863196 MeRIP-seq:(Medium) rs1488886621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496074,Human_RBP_ID_6624446,Human_RBP_ID_13106393,Human_RBP_ID_18704479,Human_RBP_ID_22959255,Human_RBP_ID_23740042 Human_Splice_Rec_1847993,Human_Splice_Rec_1848023,Human_Splice_Rec_1848051,Human_Splice_Rec_1848079,Human_Splice_Rec_1848085,Human_Splice_Rec_1848111,Human_Splice_Rec_1848127 Human_miRNA_ID_2333023,Human_miRNA_ID_2571277,Human_miRNA_ID_2966106,Human_miRNA_ID_3045014 RMVar_hsa_circ_113670,RMVar_hsa_circ_185876 97817 RMVar_ID_97817 Human_SNP_ID_628934523 m1A Human chr17 + 59912705 59912705 59912705 TTTCTTCCCAGTGGCATGGAACATTGTGAGAAATTTGAAATCTCAGAAACTAGTGTGAACAGAGG TTTCTTCCCAGTGGCATGGAACATTGTGAGAAGTTTGAAATCTCAGAAACTAGTGTGAACAGAGG A G RPS6KB1 Ensembl:ENSG00000108443 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:59910583..59913747;chr17:59910583..59912756 26863196 MeRIP-seq:(Medium) rs748806706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47289,Human_RBP_ID_900451,Human_RBP_ID_1864992,Human_RBP_ID_13106904,Human_RBP_ID_18704490,Human_RBP_ID_22656607,Human_RBP_ID_25335756 Human_Splice_Rec_1847998,Human_Splice_Rec_1847999,Human_Splice_Rec_1848026,Human_Splice_Rec_1848027,Human_Splice_Rec_1848054,Human_Splice_Rec_1848055,Human_Splice_Rec_1848082,Human_Splice_Rec_1848083,Human_Splice_Rec_1848088,Human_Splice_Rec_1848089,Human_Splice_Rec_1848116,Human_Splice_Rec_1848117,Human_Splice_Rec_1848130,Human_Splice_Rec_1848131,Human_Splice_Rec_1848158,Human_Splice_Rec_1848159 RMVar_hsa_circ_1021,RMVar_hsa_circ_113670,RMVar_hsa_circ_300684,RMVar_hsa_circ_310034,RMVar_hsa_circ_356278,RMVar_hsa_circ_185876,RMVar_hsa_circ_365799,RMVar_hsa_circ_335146,RMVar_hsa_circ_301385,RMVar_hsa_circ_283166,RMVar_hsa_circ_300241,RMVar_hsa_circ_73170,RMVar_hsa_circ_70228,RMVar_hsa_circ_185878,RMVar_hsa_circ_185879,RMVar_hsa_circ_185880,RMVar_hsa_circ_185877,RMVar_hsa_circ_280208 97818 RMVar_ID_97818 Human_SNP_ID_628942500 m1A Human chr17 + 59946914 59946914 59946914 CAGAGAGTCAATGTCATTACATAGAACACTTCAGACACAGGAAAAATAAACGTGGATTTTAAAAA CAGAGAGTCAATGTCATTACATAGAACACTTCGGACACAGGAAAAATAAACGTGGATTTTAAAAA A G AC005702.1,RPS6KB1 Ensembl:ENSG00000267318,Ensembl:ENSG00000108443 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs180515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1538977,Human_RBP_ID_1865019,Human_RBP_ID_13107741,Human_RBP_ID_23740152,Human_RBP_ID_26460826,Human_RBP_ID_26967866,Human_RBP_ID_27257758 GWAS_ID_12940,GWAS_ID_12941,GWAS_ID_12942,GWAS_ID_12943,GWAS_ID_12944,GWAS_ID_12945,GWAS_ID_12946,GWAS_ID_12947,GWAS_ID_12948,GWAS_ID_12949,GWAS_ID_12950,GWAS_ID_12951 RMVar_hsa_circ_126034,RMVar_hsa_circ_185887 97819 RMVar_ID_97819 Human_SNP_ID_628946576 m1A Human chr17 - 59964685 59964685 59964685 AGAGCTTGCGGGGTTTGCGGTTGATGGCCCCGACTGAAGGGCTGGAGGCGGTGTATGCCGCTGTT AGAGCTTGCGGGGTTTGCGGTTGATGGCCCCGGCTGAAGGGCTGGAGGCGGTGTATGCCGCTGTT T C TBC1D3P1-DHX40P1,RNFT1 Ensembl:ENSG00000267104,Ensembl:ENSG00000189050 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:59964601..59964725;chr17:59964577..59964716 26863196 MeRIP-seq:(Medium) rs572146185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465596,Human_RBP_ID_23740206 Human_Splice_Rec_1848177,Human_Splice_Rec_1848193,Human_Splice_Rec_1848207,Human_Splice_Rec_1848235,Human_Splice_Rec_1848249,Human_Splice_Rec_1848255 97820 RMVar_ID_97820 Human_SNP_ID_115028155 m1A Human chr2 - 225042322 225042322 225042322 CAGGTTCACCCGGAGCCTGTTGAGACCTGGGCAGGCGGCCGAGCTCCGGCACAGCGCCGCGTCCG CAGGTTCACCCGGAGCCTGTTGAGACCTGGGCGGGCGGCCGAGCTCCGGCACAGCGCCGCGTCCG T C DOCK10 Ensembl:ENSG00000135905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225042272..225042536 26863196 MeRIP-seq:(Medium) rs1433606132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_365767,Human_Splice_Rec_366137,Human_Splice_Rec_366177,Human_Splice_Rec_366185 97821 RMVar_ID_97821 Human_SNP_ID_115028209 m1A Human chr2 - 225042441 225042441 225042441 GTTCCGCTTCCTGAACGGCGGGTGGATAGAGAAGGTTGGCGCGGGGAAGACCGGCGGGAGGCGCG GTTCCGCTTCCTGAACGGCGGGTGGATAGAGAGGGTTGGCGCGGGGAAGACCGGCGGGAGGCGCG T C DOCK10 Ensembl:ENSG00000135905 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:224983803..225042677 26863196 MeRIP-seq:(Medium) rs1273212062 Functional Loss SNV dbSNP153 33..33 33 - - - 97822 RMVar_ID_97822 Human_SNP_ID_115143373 m1A Human chr2 - 225512646 225512639 225512647 GACAAGCAAAGAAAGATGGGAGGAAGGGAGGGAGGAAGGAAGGAAGGAGAAAAAGTAAAAAGCAA GACAAGCAAAGAAAGATGGGAGGAAGGGAGG________AAGGAAGGAGAAAAAGTAAAAAGCAA TCCTTCCTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225512567..225512748 26863196 MeRIP-seq:(Medium) rs1273709697 Functional Loss DEL dbSNP153 32..39 33 - - - 97823 RMVar_ID_97823 Human_SNP_ID_115143376 m1A Human chr2 - 225512646 225512643 225512647 GACAAGCAAAGAAAGATGGGAGGAAGGGAGGGAGGAAGGAAGGAAGGAGAAAAAGTAAAAAGCAA GACAAGCAAAGAAAGATGGGAGGAAGGGAGG____AAGGAAGGAAGGAGAAAAAGTAAAAAGCAA TCCTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225512567..225512748 26863196 MeRIP-seq:(Medium) rs1202864681 Functional Loss DEL dbSNP153 32..35 33 - - - 97824 RMVar_ID_97824 Human_SNP_ID_115143415 m1A Human chr2 - 225512713 225512713 225512713 CGAAAAAAGGAAGGAAGAGAAAGAAAGAAAAGAAAAAAGAAAAAGCAAAGCAAGACAAGCAAAGC CGAAAAAAGGAAGGAAGAGAAAGAAAGAAAAGGAAAAAGAAAAAGCAAAGCAAGACAAGCAAAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:225512531..225512740 26863196 MeRIP-seq:(Medium) rs1051407425 Functional Loss SNV dbSNP153 33..33 33 - - - 97825 RMVar_ID_97825 Human_SNP_ID_115143416 m1A Human chr2 - 225512713 225512713 225512713 CGAAAAAAGGAAGGAAGAGAAAGAAAGAAAAGAAAAAAGAAAAAGCAAAGCAAGACAAGCAAAGC CGAAAAAAGGAAGGAAGAGAAAGAAAGAAAAGCAAAAAGAAAAAGCAAAGCAAGACAAGCAAAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:225512531..225512740 26863196 MeRIP-seq:(Medium) rs1051407425 Functional Loss SNV dbSNP153 33..33 33 - - - 97826 RMVar_ID_97826 Human_SNP_ID_115143807 m1A Human chr2 - 225513520 225513520 225513520 AGCCACAGCTGCTGTCATCGTCTGTGCCCCCAACCGAGTGCAGGGACTGTGATCTCACAGAAAAG AGCCACAGCTGCTGTCATCGTCTGTGCCCCCAGCCGAGTGCAGGGACTGTGATCTCACAGAAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:225513471..225581960 26863196 MeRIP-seq:(Medium) rs763539370 Functional Loss SNV dbSNP153 33..33 33 - - - 97827 RMVar_ID_97827 Human_SNP_ID_115153382 m1A Human chr2 + 225550465 225550465 225550465 GAAGGCATTGGTGATCAGGGAAAAATAATCTCAGACGTGGTGGAGGCGTAAGCCAAATTGGGGTG GAAGGCATTGGTGATCAGGGAAAAATAATCTCGGACGTGGTGGAGGCGTAAGCCAAATTGGGGTG A G NYAP2 Ensembl:ENSG00000144460 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:225550463..225550699 26863196 MeRIP-seq:(Medium) rs1382599064 Functional Loss SNV dbSNP153 33..33 33 - - - 97828 RMVar_ID_97828 Human_SNP_ID_115161135 m1A Human chr2 - 225582505 225582505 225582505 GTTTCATGTAAGACACGTTTTCCAGCACGGGAAGCTTCGTGACCTCCAGAGGGGTAAGCGGGGAC GTTTCATGTAAGACACGTTTTCCAGCACGGGACGCTTCGTGACCTCCAGAGGGGTAAGCGGGGAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:225582461..225582700 26863196 MeRIP-seq:(Medium) rs1470176444 Functional Loss SNV dbSNP153 33..33 33 - - - 97829 RMVar_ID_97829 Human_SNP_ID_115161152 m1A Human chr2 + 225582542 225582542 225582542 GTGCTGGAAAACGTGTCTTACATGAAACAGCCAGCCGGGGCGTCGCCCTCCACGCTGCCGTCCCA GTGCTGGAAAACGTGTCTTACATGAAACAGCCCGCCGGGGCGTCGCCCTCCACGCTGCCGTCCCA A C NYAP2 Ensembl:ENSG00000144460 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:225582497..225582748 26863196 MeRIP-seq:(Medium) rs773361794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310845,RMVar_hsa_circ_207304 97830 RMVar_ID_97830 Human_SNP_ID_115161153 m1A Human chr2 + 225582542 225582542 225582542 GTGCTGGAAAACGTGTCTTACATGAAACAGCCAGCCGGGGCGTCGCCCTCCACGCTGCCGTCCCA GTGCTGGAAAACGTGTCTTACATGAAACAGCCGGCCGGGGCGTCGCCCTCCACGCTGCCGTCCCA A G NYAP2 Ensembl:ENSG00000144460 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:225582497..225582748 26863196 MeRIP-seq:(Medium) rs773361794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310845,RMVar_hsa_circ_207304 97831 RMVar_ID_97831 Human_SNP_ID_115161205 m1A Human chr2 - 225582630 225582630 225582630 TGGGGGCGACGAGGAGAGCGCAGGGGTGGCAGAGGCAGGTCCCAGGGCCGCGGCCTGCTCTTTCT TGGGGGCGACGAGGAGAGCGCAGGGGTGGCAGGGGCAGGTCCCAGGGCCGCGGCCTGCTCTTTCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:225582326..225582850 26863196 MeRIP-seq:(Medium) rs1294695343 Functional Loss SNV dbSNP153 33..33 33 - - - 97832 RMVar_ID_97832 Human_SNP_ID_115161240 m1A Human chr2 + 225582684 225582684 225582684 CGTCGCCCCCACCCCCGTCTACGCTGTACCGAACCCAGTCTCCCCATGGCTACCCTAAAAGTCAC CGTCGCCCCCACCCCCGTCTACGCTGTACCGATCCCAGTCTCCCCATGGCTACCCTAAAAGTCAC A T NYAP2 Ensembl:ENSG00000144460 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225582339..225582750 26863196 MeRIP-seq:(Medium) rs771557195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310845,RMVar_hsa_circ_207304 97833 RMVar_ID_97833 Human_SNP_ID_115465168 m1A Human chr2 + 226797824 226797824 226797824 ATGCTGGCCGGGGAGGTGGCGGTGATGCTCTCAGTGCGTGATCGGCGGGTCAGCCCCACCTGGCT ATGCTGGCCGGGGAGGTGGCGGTGATGCTCTCGGTGCGTGATCGGCGGGTCAGCCCCACCTGGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:226797582..226798000 26863196 MeRIP-seq:(Medium) rs750818294 Functional Loss SNV dbSNP153 33..33 33 - - - 97834 RMVar_ID_97834 Human_SNP_ID_115465524 m1A Human chr2 + 226798711 226798711 226798711 GCGCAGGTAGCCCACCTTGCGCACGTCCGAGAAGCCATCGCTCTCCGGAGGGCTCGCCATGCTGC GCGCAGGTAGCCCACCTTGCGCACGTCCGAGACGCCATCGCTCTCCGGAGGGCTCGCCATGCTGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:226798663..226798913 32194978 MeRIP-seq:(Medium) rs1336606386 Functional Loss SNV dbSNP153 33..33 33 - - - 97835 RMVar_ID_97835 Human_SNP_ID_115478057 m1A Human chr2 - 226849333 226849333 226849333 CTTCCTGCACATATGCTCGCTCCACCGGTGCCAGTAGGATGTCACCAGGGAATCTTCATCATCTC CTTCCTGCACATATGCTCGCTCCACCGGTGCCCGTAGGATGTCACCAGGGAATCTTCATCATCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:226849331..226849414 26863196 MeRIP-seq:(Medium) rs1465924906 Functional Loss SNV dbSNP153 33..33 33 - - - 97836 RMVar_ID_97836 Human_SNP_ID_115513250 m1A Human chr2 - 226996008 226996008 226996008 AGCTGAGGCGCCGGGGTTGGGGAGAGTAGGACAACATTCGGCCAAGGCAGCCACATCCTGTTCCT AGCTGAGGCGCCGGGGTTGGGGAGAGTAGGACCACATTCGGCCAAGGCAGCCACATCCTGTTCCT T G lnc-COL4A4-2 RNACentral:URS00008B57A2 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:226995892..226996024 26863196 MeRIP-seq:(Medium) rs1166450536 Functional Loss SNV dbSNP153 33..33 33 - - - 97837 RMVar_ID_97837 Human_SNP_ID_115527768 m1A Human chr2 - 227051151 227051151 227051151 CCTGTAACACTTCCAACTTCATCAGGTGATAAAGGAACTCCCGGGATGCAAGGGAGAAGAGGAGA CCTGTAACACTTCCAACTTCATCAGGTGATAAGGGAACTCCCGGGATGCAAGGGAGAAGAGGAGA T C COL4A4 Ensembl:ENSG00000081052 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:227051050..227051191 26863196 MeRIP-seq:(Medium) rs1559501047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_366372 97838 RMVar_ID_97838 Human_SNP_ID_115528057 m1A Human chr2 - 227052388 227052385 227052388 ATCCATAGGAGCCATAGGACCTCCCGGAGATGAAGGAGAAATGGCTATCATTTCACAAAAGGGAA ATCCATAGGAGCCATAGGACCTCCCGGAGATG___GAGAAATGGCTATCATTTCACAAAAGGGAA CCTT C COL4A4 Ensembl:ENSG00000081052 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:227052277..227052459 26863196 MeRIP-seq:(Medium) rs770269669 Functional Loss DEL dbSNP153 33..35 33 - - - Human_Splice_Rec_366370,Human_Splice_Rec_366371 97839 RMVar_ID_97839 Human_SNP_ID_115529070 m1A Human chr2 + 227056082 227056082 227056082 GGCCTTTCATTCCAGCTGGCCCGGGAGGCCCCACATCTCCCGGCTGTCCTTTCCCACCTGGAGCA GGCCTTTCATTCCAGCTGGCCCGGGAGGCCCCCCATCTCCCGGCTGTCCTTTCCCACCTGGAGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:227056035..227056156 26863196 MeRIP-seq:(Medium) rs776182609 Functional Loss SNV dbSNP153 33..33 33 - - - 97840 RMVar_ID_97840 Human_SNP_ID_115529071 m1A Human chr2 + 227056082 227056082 227056082 GGCCTTTCATTCCAGCTGGCCCGGGAGGCCCCACATCTCCCGGCTGTCCTTTCCCACCTGGAGCA GGCCTTTCATTCCAGCTGGCCCGGGAGGCCCCGCATCTCCCGGCTGTCCTTTCCCACCTGGAGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:227056035..227056156 26863196 MeRIP-seq:(Medium) rs776182609 Functional Loss SNV dbSNP153 33..33 33 - - - 97841 RMVar_ID_97841 Human_SNP_ID_115547512 m1A Human chr2 - 227128617 227128617 227128617 GTCATGAGAAGGACATGGAGAATGAGGGAAAGAGGGTGACAAGGCTGGCAGCTGGATGGCGAGCT GTCATGAGAAGGACATGGAGAATGAGGGAAAGCGGGTGACAAGGCTGGCAGCTGGATGGCGAGCT T G COL4A4 Ensembl:ENSG00000081052 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:227128614..227128777 26863196 MeRIP-seq:(Medium) rs541260849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372430,RMVar_hsa_circ_207319,RMVar_hsa_circ_66732 97842 RMVar_ID_97842 Human_SNP_ID_115597475 m1A Human chr2 + 227325349 227325349 227325349 GTCCCTGGGCGCCTCCGTGCTCTCAGCCAACCACCTCTGAGAGCGCCCACTCGAGCGCCCCGGGA GTCCCTGGGCGCCTCCGTGCTCTCAGCCAACCGCCTCTGAGAGCGCCCACTCGAGCGCCCCGGGA A G MFF Ensembl:ENSG00000168958 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:227325300..227325590 26863196 MeRIP-seq:(Medium) rs7588961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622967,Human_RBP_ID_17392884,Human_RBP_ID_22451996 Human_Splice_Rec_366859,Human_Splice_Rec_366865,Human_Splice_Rec_366873,Human_Splice_Rec_366879,Human_Splice_Rec_366899,Human_Splice_Rec_366911,Human_Splice_Rec_366919,Human_Splice_Rec_366935,Human_Splice_Rec_366941,Human_Splice_Rec_366957,Human_Splice_Rec_366973,Human_Splice_Rec_366983,Human_Splice_Rec_366997,Human_Splice_Rec_367003,Human_Splice_Rec_367007,Human_Splice_Rec_367015,Human_Splice_Rec_367023,Human_Splice_Rec_367037 GWAS_ID_12952,GWAS_ID_12953,GWAS_ID_12954,GWAS_ID_12955 97843 RMVar_ID_97843 Human_SNP_ID_115601553 m1A Human chr2 - 227340375 227340375 227340375 AGATAAAATGCTAGTGCTTCTACTCACAGAGAATCATTTCTGACCAGCTGTCCATTTTGGCGAAC AGATAAAATGCTAGTGCTTCTACTCACAGAGACTCATTTCTGACCAGCTGTCCATTTTGGCGAAC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:227340292..227340443 32194978 MeRIP-seq:(Medium) rs1212420362 Functional Loss SNV dbSNP153 33..33 33 - - - 97844 RMVar_ID_97844 Human_SNP_ID_115635053 m1A Human chr2 - 227472209 227472209 227472209 GGTACGCGGGCTGACGGGCCACACCAACCGGCACAGCCGGGACAACCGCCGCCGCCGCCGCCACC GGTACGCGGGCTGACGGGCCACACCAACCGGCTCAGCCGGGACAACCGCCGCCGCCGCCGCCACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:227472151..227472413 26863196 MeRIP-seq:(Medium) rs1435856863 Functional Loss SNV dbSNP153 33..33 33 - - - 97845 RMVar_ID_97845 Human_SNP_ID_115635061 m1A Human chr2 - 227472221 227472221 227472221 CCCGGGCGCTGTGGTACGCGGGCTGACGGGCCACACCAACCGGCACAGCCGGGACAACCGCCGCC CCCGGGCGCTGTGGTACGCGGGCTGACGGGCCTCACCAACCGGCACAGCCGGGACAACCGCCGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:227472151..227472401 26863196 MeRIP-seq:(Medium) rs1559160249 Functional Loss SNV dbSNP153 33..33 33 - - - 97846 RMVar_ID_97846 Human_SNP_ID_115635077 m1A Human chr2 - 227472293 227472293 227472293 CGCCCTCCGTCTGCGCGCGCCGCCCGCGCCGGACCCGGCCGCAGCGGCTTGGCTGTACTGGGCTC CGCCCTCCGTCTGCGCGCGCCGCCCGCGCCGGGCCCGGCCGCAGCGGCTTGGCTGTACTGGGCTC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:227472201..227472351 26863410 MeRIP-seq:(Medium) rs1369573628 Functional Loss SNV dbSNP153 33..33 33 - - - 97847 RMVar_ID_97847 Human_SNP_ID_116072245 m1A Human chr2 - 229180829 229180829 229180829 CGAAGGGACAGGCAATGGCCTCCCTTGCCCTCAGCGGATCGAAAGGGAGTCGGGTTCAGATCCCC CGAAGGGACAGGCAATGGCCTCCCTTGCCCTCGGCGGATCGAAAGGGAGTCGGGTTCAGATCCCC T C PID1 Ensembl:ENSG00000153823 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:229180731..229181090;chr2:229180738..229181097;chr2:229180738..229180899 26863196 MeRIP-seq:(Medium) rs78860008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270321,Human_RBP_ID_280687,Human_RBP_ID_1098468,Human_RBP_ID_1197384,Human_RBP_ID_1584090,Human_RBP_ID_2625438,Human_RBP_ID_4598728,Human_RBP_ID_5199903,Human_RBP_ID_5275690,Human_RBP_ID_5422822,Human_RBP_ID_5589059,Human_RBP_ID_6972677,Human_RBP_ID_8513414,Human_RBP_ID_8846057,Human_RBP_ID_9103674,Human_RBP_ID_13789207,Human_RBP_ID_17015051,Human_RBP_ID_17063690,Human_RBP_ID_17068869,Human_RBP_ID_17135121,Human_RBP_ID_17192636,Human_RBP_ID_17698608,Human_RBP_ID_17966823,Human_RBP_ID_18180338,Human_RBP_ID_18200861,Human_RBP_ID_18208876,Human_RBP_ID_18755489,Human_RBP_ID_20437284,Human_RBP_ID_22422690,Human_RBP_ID_22990011,Human_RBP_ID_23182310,Human_RBP_ID_23310660,Human_RBP_ID_23855889,Human_RBP_ID_26488240,Human_RBP_ID_26663912,Human_RBP_ID_26749885,Human_RBP_ID_27007556,Human_RBP_ID_27158802,Human_RBP_ID_27287271 RMVar_hsa_circ_354719,RMVar_hsa_circ_361298,RMVar_hsa_circ_207384 97848 RMVar_ID_97848 Human_SNP_ID_116072253 m1A Human chr2 - 229180852 229180852 229180852 TGAGAGATGGGCGAGCGCCGTTCCGAAGGGACAGGCAATGGCCTCCCTTGCCCTCAGCGGATCGA TGAGAGATGGGCGAGCGCCGTTCCGAAGGGACGGGCAATGGCCTCCCTTGCCCTCAGCGGATCGA T C PID1 Ensembl:ENSG00000153823 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:229180803..229180885 26863196 MeRIP-seq:(Medium) rs62190429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270321,Human_RBP_ID_280687,Human_RBP_ID_545430,Human_RBP_ID_1022178,Human_RBP_ID_1098470,Human_RBP_ID_1134600,Human_RBP_ID_1197384,Human_RBP_ID_1303007,Human_RBP_ID_1379511,Human_RBP_ID_1584090,Human_RBP_ID_1912150,Human_RBP_ID_2673800,Human_RBP_ID_3617518,Human_RBP_ID_4598728,Human_RBP_ID_5194502,Human_RBP_ID_5262753,Human_RBP_ID_5275692,Human_RBP_ID_5422822,Human_RBP_ID_5444560,Human_RBP_ID_5470502,Human_RBP_ID_5501764,Human_RBP_ID_5589061,Human_RBP_ID_6893348,Human_RBP_ID_8107428,Human_RBP_ID_8260212,Human_RBP_ID_8513414,Human_RBP_ID_8846057,Human_RBP_ID_9103676,Human_RBP_ID_9259413,Human_RBP_ID_9295599,Human_RBP_ID_9975034,Human_RBP_ID_10484019,Human_RBP_ID_13789207,Human_RBP_ID_17015051,Human_RBP_ID_17063692,Human_RBP_ID_17068870,Human_RBP_ID_17135123,Human_RBP_ID_17192638,Human_RBP_ID_17280429,Human_RBP_ID_17390490,Human_RBP_ID_17506341,Human_RBP_ID_17698608,Human_RBP_ID_17951812,Human_RBP_ID_18180894,Human_RBP_ID_18200861,Human_RBP_ID_18208876,Human_RBP_ID_18315185,Human_RBP_ID_18443157,Human_RBP_ID_18515593,Human_RBP_ID_18534326,Human_RBP_ID_18755489,Human_RBP_ID_20534620,Human_RBP_ID_21931272,Human_RBP_ID_22006703,Human_RBP_ID_22248432,Human_RBP_ID_22393209,Human_RBP_ID_22422690,Human_RBP_ID_22505170,Human_RBP_ID_22816686,Human_RBP_ID_22990011,Human_RBP_ID_23133404,Human_RBP_ID_23182310,Human_RBP_ID_23281294,Human_RBP_ID_23311136,Human_RBP_ID_23855889,Human_RBP_ID_24533340,Human_RBP_ID_24540265,Human_RBP_ID_25518917,Human_RBP_ID_26480236,Human_RBP_ID_26663912,Human_RBP_ID_26749885,Human_RBP_ID_27007556,Human_RBP_ID_27158802,Human_RBP_ID_27287271,Human_RBP_ID_27478137,Human_RBP_ID_27563619,Human_RBP_ID_27693373 RMVar_hsa_circ_354719,RMVar_hsa_circ_361298,RMVar_hsa_circ_207384 97849 RMVar_ID_97849 Human_SNP_ID_116217042 m1A Human chr2 - 229780505 229780501 229780505 AGGCCGTGGTAAGAACTGGAGCTGTGCTTTGAATGAGATGGAAAACCTTTGGAAAGTAGCAAAGG AGGCCGTGGTAAGAACTGGAGCTGTGCTTTGA____GATGGAAAACCTTTGGAAAGTAGCAAAGG CTCAT C TRIP12 Ensembl:ENSG00000153827 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:229780499..229780662 26863196 MeRIP-seq:(Medium) rs1320589783 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23855945 RMVar_hsa_circ_3268,RMVar_hsa_circ_19019,RMVar_hsa_circ_353311,RMVar_hsa_circ_87583,RMVar_hsa_circ_108938,RMVar_hsa_circ_207397,RMVar_hsa_circ_116202,RMVar_hsa_circ_79880,RMVar_hsa_circ_15604,RMVar_hsa_circ_99423,RMVar_hsa_circ_207399,RMVar_hsa_circ_207400,RMVar_hsa_circ_207398,RMVar_hsa_circ_368500,RMVar_hsa_circ_207401,RMVar_hsa_circ_339035,RMVar_hsa_circ_207402,RMVar_hsa_circ_11803,RMVar_hsa_circ_127149,RMVar_hsa_circ_26484,RMVar_hsa_circ_42279,RMVar_hsa_circ_297828,RMVar_hsa_circ_378043,RMVar_hsa_circ_266805,RMVar_hsa_circ_269142 97850 RMVar_ID_97850 Human_SNP_ID_116226672 m1A Human chr2 - 229818507 229818507 229818507 AGATAATAATTATTTTTTTCTCTAAAGGTTCTAAGGCCCAGCAGCTACTACAAGGATTGCAAGCC AGATAATAATTATTTTTTTCTCTAAAGGTTCTGAGGCCCAGCAGCTACTACAAGGATTGCAAGCC T C TRIP12 Ensembl:ENSG00000153827 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:229818457..229830805 32194978 MeRIP-seq:(Medium) rs1033538724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59773,Human_RBP_ID_922362,Human_RBP_ID_4598916,Human_RBP_ID_22360190 Human_Splice_Rec_367620,Human_Splice_Rec_367694,Human_Splice_Rec_367774,Human_Splice_Rec_367880 RMVar_hsa_circ_108938,RMVar_hsa_circ_4576,RMVar_hsa_circ_5569,RMVar_hsa_circ_15604,RMVar_hsa_circ_207400,RMVar_hsa_circ_86038,RMVar_hsa_circ_62599,RMVar_hsa_circ_207406,RMVar_hsa_circ_91538,RMVar_hsa_circ_51495,RMVar_hsa_circ_126478,RMVar_hsa_circ_101366,RMVar_hsa_circ_207407,RMVar_hsa_circ_207408,RMVar_hsa_circ_127495,RMVar_hsa_circ_70364,RMVar_hsa_circ_112011,RMVar_hsa_circ_207409,RMVar_hsa_circ_207410,RMVar_hsa_circ_116773,RMVar_hsa_circ_207420,RMVar_hsa_circ_207423,RMVar_hsa_circ_207422,RMVar_hsa_circ_81600,RMVar_hsa_circ_369709,RMVar_hsa_circ_30008,RMVar_hsa_circ_15529,RMVar_hsa_circ_96037,RMVar_hsa_circ_207429,RMVar_hsa_circ_48409,RMVar_hsa_circ_317515,RMVar_hsa_circ_207430,RMVar_hsa_circ_13213,RMVar_hsa_circ_320436,RMVar_hsa_circ_78232,RMVar_hsa_circ_43535,RMVar_hsa_circ_10018,RMVar_hsa_circ_207433,RMVar_hsa_circ_75707,RMVar_hsa_circ_78007,RMVar_hsa_circ_100170,RMVar_hsa_circ_207434,RMVar_hsa_circ_207437,RMVar_hsa_circ_360882,RMVar_hsa_circ_83381,RMVar_hsa_circ_207438,RMVar_hsa_circ_207439,RMVar_hsa_circ_355568,RMVar_hsa_circ_124074,RMVar_hsa_circ_322188,RMVar_hsa_circ_62327,RMVar_hsa_circ_64837,RMVar_hsa_circ_13646,RMVar_hsa_circ_207441,RMVar_hsa_circ_207442,RMVar_hsa_circ_341547,RMVar_hsa_circ_207445,RMVar_hsa_circ_93959,RMVar_hsa_circ_353009,RMVar_hsa_circ_375578,RMVar_hsa_circ_349663,RMVar_hsa_circ_316470,RMVar_hsa_circ_340023,RMVar_hsa_circ_302932,RMVar_hsa_circ_207446,RMVar_hsa_circ_207448,RMVar_hsa_circ_207449,RMVar_hsa_circ_207447,RMVar_hsa_circ_207450 97851 RMVar_ID_97851 Human_SNP_ID_116237191 m1A Human chr2 - 229859267 229859267 229859267 CACAATCACCATCAACAAGCAAGGCTCATACCAGGAAGAGTGGGGCCACTGGCGGTTCACGGAGT CACAATCACCATCAACAAGCAAGGCTCATACCGGGAAGAGTGGGGCCACTGGCGGTTCACGGAGT T C TRIP12 Ensembl:ENSG00000153827 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:229859013..229859483 26863196 MeRIP-seq:(Medium) rs376223742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59785,Human_RBP_ID_243075,Human_RBP_ID_829581,Human_RBP_ID_5528263,Human_RBP_ID_5589067,Human_RBP_ID_9388063,Human_RBP_ID_18533491,Human_RBP_ID_24545941,Human_RBP_ID_26340318,Human_RBP_ID_27007631 RMVar_hsa_circ_108938,RMVar_hsa_circ_207400,RMVar_hsa_circ_51495,RMVar_hsa_circ_127495,RMVar_hsa_circ_112011,RMVar_hsa_circ_207409,RMVar_hsa_circ_116773,RMVar_hsa_circ_207420,RMVar_hsa_circ_207423,RMVar_hsa_circ_207422,RMVar_hsa_circ_81600,RMVar_hsa_circ_369709,RMVar_hsa_circ_96037,RMVar_hsa_circ_207429,RMVar_hsa_circ_48409,RMVar_hsa_circ_207430,RMVar_hsa_circ_78232,RMVar_hsa_circ_207433,RMVar_hsa_circ_78007,RMVar_hsa_circ_100170,RMVar_hsa_circ_207437,RMVar_hsa_circ_207439,RMVar_hsa_circ_124074,RMVar_hsa_circ_72910,RMVar_hsa_circ_64837,RMVar_hsa_circ_207442,RMVar_hsa_circ_207445,RMVar_hsa_circ_93959,RMVar_hsa_circ_353009,RMVar_hsa_circ_302932,RMVar_hsa_circ_207446,RMVar_hsa_circ_343281,RMVar_hsa_circ_285171,RMVar_hsa_circ_207456,RMVar_hsa_circ_207454,RMVar_hsa_circ_365127,RMVar_hsa_circ_299177,RMVar_hsa_circ_279427,RMVar_hsa_circ_289036,RMVar_hsa_circ_207455,RMVar_hsa_circ_302291,RMVar_hsa_circ_288068,RMVar_hsa_circ_207461,RMVar_hsa_circ_207458,RMVar_hsa_circ_207459,RMVar_hsa_circ_274764,RMVar_hsa_circ_350673,RMVar_hsa_circ_207457,RMVar_hsa_circ_302556,RMVar_hsa_circ_207462,RMVar_hsa_circ_85269,RMVar_hsa_circ_207460,RMVar_hsa_circ_207463 97852 RMVar_ID_97852 Human_SNP_ID_116237192 m1A Human chr2 - 229859267 229859267 229859267 CACAATCACCATCAACAAGCAAGGCTCATACCAGGAAGAGTGGGGCCACTGGCGGTTCACGGAGT CACAATCACCATCAACAAGCAAGGCTCATACCCGGAAGAGTGGGGCCACTGGCGGTTCACGGAGT T G TRIP12 Ensembl:ENSG00000153827 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:229859013..229859483 26863196 MeRIP-seq:(Medium) rs376223742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59785,Human_RBP_ID_243075,Human_RBP_ID_829581,Human_RBP_ID_5528263,Human_RBP_ID_5589067,Human_RBP_ID_9388063,Human_RBP_ID_18533491,Human_RBP_ID_24545941,Human_RBP_ID_26340318,Human_RBP_ID_27007631 RMVar_hsa_circ_108938,RMVar_hsa_circ_207400,RMVar_hsa_circ_51495,RMVar_hsa_circ_127495,RMVar_hsa_circ_112011,RMVar_hsa_circ_207409,RMVar_hsa_circ_116773,RMVar_hsa_circ_207420,RMVar_hsa_circ_207423,RMVar_hsa_circ_207422,RMVar_hsa_circ_81600,RMVar_hsa_circ_369709,RMVar_hsa_circ_96037,RMVar_hsa_circ_207429,RMVar_hsa_circ_48409,RMVar_hsa_circ_207430,RMVar_hsa_circ_78232,RMVar_hsa_circ_207433,RMVar_hsa_circ_78007,RMVar_hsa_circ_100170,RMVar_hsa_circ_207437,RMVar_hsa_circ_207439,RMVar_hsa_circ_124074,RMVar_hsa_circ_72910,RMVar_hsa_circ_64837,RMVar_hsa_circ_207442,RMVar_hsa_circ_207445,RMVar_hsa_circ_93959,RMVar_hsa_circ_353009,RMVar_hsa_circ_302932,RMVar_hsa_circ_207446,RMVar_hsa_circ_343281,RMVar_hsa_circ_285171,RMVar_hsa_circ_207456,RMVar_hsa_circ_207454,RMVar_hsa_circ_365127,RMVar_hsa_circ_299177,RMVar_hsa_circ_279427,RMVar_hsa_circ_289036,RMVar_hsa_circ_207455,RMVar_hsa_circ_302291,RMVar_hsa_circ_288068,RMVar_hsa_circ_207461,RMVar_hsa_circ_207458,RMVar_hsa_circ_207459,RMVar_hsa_circ_274764,RMVar_hsa_circ_350673,RMVar_hsa_circ_207457,RMVar_hsa_circ_302556,RMVar_hsa_circ_207462,RMVar_hsa_circ_85269,RMVar_hsa_circ_207460,RMVar_hsa_circ_207463 97853 RMVar_ID_97853 Human_SNP_ID_116253089 m1A Human chr2 + 229921185 229921185 229921185 CATCCTCCCTCAGCCTCAACTTCCCACGGCTTAAAAAACTGCCCCGCGCAGACCCCGTCTCCGGG CATCCTCCCTCAGCCTCAACTTCCCACGGCTTTAAAAACTGCCCCGCGCAGACCCCGTCTCCGGG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:229921163..229921574 26863196 MeRIP-seq:(Medium) rs1466836607 Functional Loss SNV dbSNP153 33..33 33 - - - 97854 RMVar_ID_97854 Human_SNP_ID_116253376 m1A Human chr2 - 229921931 229921931 229921931 GCGCCGCTGGGGGGGGTGGGGGGAGCTAGTGGAAGTTACTGCCGCGCCACCGAGTCCGGACCGGA GCGCCGCTGGGGGGGGTGGGGGGAGCTAGTGGTAGTTACTGCCGCGCCACCGAGTCCGGACCGGA T A TRIP12 Ensembl:ENSG00000153827 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:229921843..229922206 26863196 MeRIP-seq:(Medium) rs1328476421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243078,Human_RBP_ID_778278,Human_RBP_ID_922375,Human_RBP_ID_3958528,Human_RBP_ID_4623896,Human_RBP_ID_5147241,Human_RBP_ID_8234568,Human_RBP_ID_8942717,Human_RBP_ID_9296963,Human_RBP_ID_9428961,Human_RBP_ID_18422033,Human_RBP_ID_18948614,Human_RBP_ID_24560273,Human_RBP_ID_26340319,Human_RBP_ID_26770227,Human_RBP_ID_27818026 Human_Splice_Rec_367607,Human_Splice_Rec_367685,Human_Splice_Rec_367759,Human_Splice_Rec_367867,Human_Splice_Rec_367903,Human_Splice_Rec_367935 RMVar_hsa_circ_207445,RMVar_hsa_circ_93959 97855 RMVar_ID_97855 Human_SNP_ID_116253870 m1A Human chr2 - 229922827 229922827 229922827 AAGGAGCACGCGGCACCGCGGGGAGGCAGAGAAGGCTTGCCAGGGACTAGCCGGGCTCGGGGAGA AAGGAGCACGCGGCACCGCGGGGAGGCAGAGAGGGCTTGCCAGGGACTAGCCGGGCTCGGGGAGA T C TRIP12 Ensembl:ENSG00000153827 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:229922777..229922933 26863196 MeRIP-seq:(Medium) rs1317346642 Functional Loss SNV dbSNP153 33..33 33 - - - 97856 RMVar_ID_97856 Human_SNP_ID_116324582 m1A Human chr2 - 230209981 230209981 230209981 GTCAGAGATAAGAGATAATTCTCCAGAACCAAATGACCCAGAAGAGCCCCAGGAGGTGTCCAGCA GTCAGAGATAAGAGATAATTCTCCAGAACCAACTGACCCAGAAGAGCCCCAGGAGGTGTCCAGCA T G SP110 Ensembl:ENSG00000135899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:230209903..230210055 26863196 MeRIP-seq:(Medium) rs1159803414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_919410 Human_Splice_Rec_368058,Human_Splice_Rec_368059,Human_Splice_Rec_368096,Human_Splice_Rec_368097,Human_Splice_Rec_368132,Human_Splice_Rec_368133,Human_Splice_Rec_368160,Human_Splice_Rec_368161,Human_Splice_Rec_368190,Human_Splice_Rec_368191,Human_Splice_Rec_368210,Human_Splice_Rec_368211,Human_Splice_Rec_368222,Human_Splice_Rec_368223 RMVar_hsa_circ_55027,RMVar_hsa_circ_364687 97857 RMVar_ID_97857 Human_SNP_ID_116352303 m1A Human chr2 + 230327248 230327248 230327248 CTGGGGAGCTCATAGGCCAGGCTCTGACACCCAGGCAGGGCCTAGGGTGGGACGATGGCAGGTGG CTGGGGAGCTCATAGGCCAGGCTCTGACACCCCGGCAGGGCCTAGGGTGGGACGATGGCAGGTGG A C SP140L Ensembl:ENSG00000185404 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:230327198..230327318 26863196 MeRIP-seq:(Medium) rs1277456150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_368501,Human_Splice_Rec_368529,Human_Splice_Rec_368565,Human_Splice_Rec_368599 RMVar_hsa_circ_107132,RMVar_hsa_circ_78129,RMVar_hsa_circ_207479,RMVar_hsa_circ_124845,RMVar_hsa_circ_207481,RMVar_hsa_circ_207482 97858 RMVar_ID_97858 Human_SNP_ID_116352311 m1A Human chr2 - 230327263 230327263 230327263 CTCAGGTCGCTGCCCCCACCTGCCATCGTCCCACCCTAGGCCCTGCCTGGGTGTCAGAGCCTGGC CTCAGGTCGCTGCCCCCACCTGCCATCGTCCCCCCCTAGGCCCTGCCTGGGTGTCAGAGCCTGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:230327215..230327350 26863196 MeRIP-seq:(Medium) rs780416434 Functional Loss SNV dbSNP153 33..33 33 - - - 97859 RMVar_ID_97859 Human_SNP_ID_116373932 m1A Human chr2 + 230416261 230416248 230416261 GCAGGCTGGGCCGACTGAGGGGCTCAGAGGCCAGGCTCTGAGGCCCACGCAGGGCCTAGGGTGGG GCAGGCTGGGCCGACTGAGG_____________GGCTCTGAGGCCCACGCAGGGCCTAGGGTGGG GGGCTCAGAGGCCA G SP100 Ensembl:ENSG00000067066 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:230416201..230416371 26863196 MeRIP-seq:(Medium) rs760503746 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_4623897,Human_RBP_ID_8513564,Human_RBP_ID_27818032 Human_Splice_Rec_368681,Human_Splice_Rec_368729,Human_Splice_Rec_368755,Human_Splice_Rec_368811,Human_Splice_Rec_368821,Human_Splice_Rec_368847,Human_Splice_Rec_368875 RMVar_hsa_circ_102102,RMVar_hsa_circ_90878,RMVar_hsa_circ_207487,RMVar_hsa_circ_207489,RMVar_hsa_circ_80716,RMVar_hsa_circ_207490 97860 RMVar_ID_97860 Human_SNP_ID_116373936 m1A Human chr2 + 230416261 230416261 230416261 GCAGGCTGGGCCGACTGAGGGGCTCAGAGGCCAGGCTCTGAGGCCCACGCAGGGCCTAGGGTGGG GCAGGCTGGGCCGACTGAGGGGCTCAGAGGCCGGGCTCTGAGGCCCACGCAGGGCCTAGGGTGGG A G SP100 Ensembl:ENSG00000067066 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:230416201..230416371 26863196 MeRIP-seq:(Medium) rs1474346699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623897,Human_RBP_ID_8513564,Human_RBP_ID_27818032 Human_Splice_Rec_368681,Human_Splice_Rec_368729,Human_Splice_Rec_368755,Human_Splice_Rec_368811,Human_Splice_Rec_368821,Human_Splice_Rec_368847,Human_Splice_Rec_368875 RMVar_hsa_circ_102102,RMVar_hsa_circ_90878,RMVar_hsa_circ_207487,RMVar_hsa_circ_207489,RMVar_hsa_circ_80716,RMVar_hsa_circ_207490 97861 RMVar_ID_97861 Human_SNP_ID_116374230 m1A Human chr2 + 230417542 230417542 230417542 CTTGTCTCTAAACCTTAAAAATGTAATTATTGAGGCAAAGGGTCCAGTTATTTACTTGGTCCTGC CTTGTCTCTAAACCTTAAAAATGTAATTATTGGGGCAAAGGGTCCAGTTATTTACTTGGTCCTGC A G SP100 Ensembl:ENSG00000067066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:230417540..230417632 26863196 MeRIP-seq:(Medium) rs1012691278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102102,RMVar_hsa_circ_90878,RMVar_hsa_circ_207487,RMVar_hsa_circ_207489,RMVar_hsa_circ_80716,RMVar_hsa_circ_207490 97862 RMVar_ID_97862 Human_SNP_ID_116412611 m1A Human chr2 - 230573840 230573840 230573840 ATCCAGGTTCTGCAGCAGCAGGCAGATGATGCAGAGGAGCGAGCTGAGCACCTCCAGCGAGAAGT ATCCAGGTTCTGCAGCAGCAGGCAGATGATGCCGAGGAGCGAGCTGAGCACCTCCAGCGAGAAGT T G AC010149.1 Ensembl:ENSG00000235419 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:230573803..230573868 26863196 MeRIP-seq:(Medium) rs765667477 Functional Loss SNV dbSNP153 33..33 33 - - - 97863 RMVar_ID_97863 Human_SNP_ID_116448955 m1A Human chr2 + 230712897 230712897 230712897 CTCGGGCCGCAAGCGGGGCGAGGGGTTCGGGGAGCGGCGCGGCCTGGGAGACACAGAGCCTTCAG CTCGGGCCGCAAGCGGGGCGAGGGGTTCGGGGGGCGGCGCGGCCTGGGAGACACAGAGCCTTCAG A G CAB39 Ensembl:ENSG00000135932 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:230712851..230713559;chr2:230712851..230713270 26863196 MeRIP-seq:(Medium) rs1169152856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243651,Human_RBP_ID_774135,Human_RBP_ID_4623898,Human_RBP_ID_5146704,Human_RBP_ID_5470513,Human_RBP_ID_8852211,Human_RBP_ID_9330830,Human_RBP_ID_9428963,Human_RBP_ID_18422036,Human_RBP_ID_18462694,Human_RBP_ID_26786468 97864 RMVar_ID_97864 Human_SNP_ID_116448961 m1A Human chr2 - 230712909 230712909 230712909 CCGCCCCGGCGCCTGAAGGCTCTGTGTCTCCCAGGCCGCGCCGCTCCCCGAACCCCTCGCCCCGC CCGCCCCGGCGCCTGAAGGCTCTGTGTCTCCCGGGCCGCGCCGCTCCCCGAACCCCTCGCCCCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:230712851..230713275;chr2:230712851..230713609 26863196 MeRIP-seq:(Medium) rs918334718 Functional Loss SNV dbSNP153 33..33 33 - - - 97865 RMVar_ID_97865 Human_SNP_ID_116448989 m1A Human chr2 - 230712958 230712958 230712958 GCGGCTGCTGCTGTGGGGCCCGGCGCCGCCTTAGTCTTCGCCTGTGCCCCCGCCCCGGCGCCTGA GCGGCTGCTGCTGTGGGGCCCGGCGCCGCCTTGGTCTTCGCCTGTGCCCCCGCCCCGGCGCCTGA T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:230712863..230713093 26863410 MeRIP-seq:(Medium) rs891878438 Functional Loss SNV dbSNP153 33..33 33 - - - 97866 RMVar_ID_97866 Human_SNP_ID_116449312 m1A Human chr2 - 230713819 230713819 230713819 CACACCAGAGCCTAAGCTCCTCGGGGGAGGGGACCGGGGCCCGCTTCACCTTTGAATCCCTCCGG CACACCAGAGCCTAAGCTCCTCGGGGGAGGGGCCCGGGGCCCGCTTCACCTTTGAATCCCTCCGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:230712993..230714006 32194978 MeRIP-seq:(Medium) rs1326942326 Functional Loss SNV dbSNP153 33..33 33 - - - 97867 RMVar_ID_97867 Human_SNP_ID_116449385 m1A Human chr2 + 230714055 230714055 230714055 CCTGATGGGATTTAGGAGAGGAGGATTGCAGAAGAGGTGTGTGGAAGGGGTAGCAAAAGCGAGAA CCTGATGGGATTTAGGAGAGGAGGATTGCAGACGAGGTGTGTGGAAGGGGTAGCAAAAGCGAGAA A C CAB39 Ensembl:ENSG00000135932 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:230714054..230760075;chr2:230714054..230760054 26863196 MeRIP-seq:(Medium) rs982425654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13791132 Human_Splice_Rec_369093 97868 RMVar_ID_97868 Human_SNP_ID_116452299 m1A Human chr2 - 230725378 230725378 230725378 GATCAAGATGACAACCTCCCAAAAGCACCGAGACTTCGTGGCAGAGCCCATGGGGGAGAAGCCAG GATCAAGATGACAACCTCCCAAAAGCACCGAGGCTTCGTGGCAGAGCCCATGGGGGAGAAGCCAG T C BANF1P3 Ensembl:ENSG00000237758 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:230725278..230725433 26863410 MeRIP-seq:(Medium) rs1253657925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1855437,Human_miRNA_ID_1908290 97869 RMVar_ID_97869 Human_SNP_ID_116487446 m1A Human chr2 + 230864992 230864992 230864992 GGCGGAGGCAGAGACCGAGGCTGCACCGGCAGAGGCTGCGGGGCGGACGCGCGGGCCGGCGCAGC GGCGGAGGCAGAGACCGAGGCTGCACCGGCAGGGGCTGCGGGGCGGACGCGCGGGCCGGCGCAGC A G ITM2C Ensembl:ENSG00000135916 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:230864926..230865180;chr2:230864922..230865180;chr2:230864916..230865190;chr2:230864926..230865195 26863196 MeRIP-seq:(Medium) rs752223692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4599194,Human_RBP_ID_8942718,Human_RBP_ID_20619170,Human_RBP_ID_22450947 Human_Splice_Rec_369128 97870 RMVar_ID_97870 Human_SNP_ID_116487486 m1A Human chr2 + 230865062 230865062 230865062 TGAAGATTAGCTTCCAGCCCGCCGTGGCTGGCATCAAGGGCGACAAGGCTGACAAGGCGTCGGCG TGAAGATTAGCTTCCAGCCCGCCGTGGCTGGCGTCAAGGGCGACAAGGCTGACAAGGCGTCGGCG A G ITM2C Ensembl:ENSG00000135916 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:230864951..230865150 26863410 MeRIP-seq:(Medium) rs776962500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545584,Human_RBP_ID_4599200,Human_RBP_ID_5470514,Human_RBP_ID_5501775,Human_RBP_ID_9103786,Human_RBP_ID_17952023 Human_Splice_Rec_369129,Human_Splice_Rec_369141,Human_Splice_Rec_369151,Human_Splice_Rec_369159 97871 RMVar_ID_97871 Human_SNP_ID_116489830 m1A Human chr2 - 230873347 230873347 230873347 CCCTCCCCTGGAAATCCCCCCTTCCCTAAGTCAGGCTTCACCTGCTGGCTGGGCCCGGAGGGAGT CCCTCCCCTGGAAATCCCCCCTTCCCTAAGTCGGGCTTCACCTGCTGGCTGGGCCCGGAGGGAGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:230873345..230873521 26863196 MeRIP-seq:(Medium) rs888022708 Functional Loss SNV dbSNP153 33..33 33 - - - 97872 RMVar_ID_97872 Human_SNP_ID_116490950 m1A Human chr2 + 230876855 230876855 230876855 CTGCAGAGACTGACCCAACCCCTTCTCCTGCCAGGGTCTGACTGCGTACCATGATATCTCCCTGG CTGCAGAGACTGACCCAACCCCTTCTCCTGCCGGGGTCTGACTGCGTACCATGATATCTCCCTGG A G ITM2C Ensembl:ENSG00000135916 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:230876851..230876925 32194978 MeRIP-seq:(Medium) rs111590996 Functional Loss SNV dbSNP153 33..33 33 - - - 97873 RMVar_ID_97873 Human_SNP_ID_116490951 m1A Human chr2 + 230876855 230876855 230876855 CTGCAGAGACTGACCCAACCCCTTCTCCTGCCAGGGTCTGACTGCGTACCATGATATCTCCCTGG CTGCAGAGACTGACCCAACCCCTTCTCCTGCCTGGGTCTGACTGCGTACCATGATATCTCCCTGG A T ITM2C Ensembl:ENSG00000135916 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:230876851..230876925 32194978 MeRIP-seq:(Medium) rs111590996 Functional Loss SNV dbSNP153 33..33 33 - - - 97874 RMVar_ID_97874 Human_SNP_ID_116491233 m1A Human chr2 + 230877541 230877541 230877541 GGAAAGACACCTACCGGCTCCGGCGCCGGGCAACGCGGAGGCGTGAGTGGCTGGCTTCACCCACA GGAAAGACACCTACCGGCTCCGGCGCCGGGCAGCGCGGAGGCGTGAGTGGCTGGCTTCACCCACA A G ITM2C Ensembl:ENSG00000135916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:230877449..230877575 26863196 MeRIP-seq:(Medium) rs748984665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22766302 Human_Splice_Rec_369149,Human_Splice_Rec_369157,Human_Splice_Rec_369165,Human_Splice_Rec_369181 97875 RMVar_ID_97875 Human_SNP_ID_116491234 m1A Human chr2 + 230877541 230877541 230877541 GGAAAGACACCTACCGGCTCCGGCGCCGGGCAACGCGGAGGCGTGAGTGGCTGGCTTCACCCACA GGAAAGACACCTACCGGCTCCGGCGCCGGGCATCGCGGAGGCGTGAGTGGCTGGCTTCACCCACA A T ITM2C Ensembl:ENSG00000135916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:230877449..230877575 26863196 MeRIP-seq:(Medium) rs748984665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22766302 Human_Splice_Rec_369149,Human_Splice_Rec_369157,Human_Splice_Rec_369165,Human_Splice_Rec_369181 97876 RMVar_ID_97876 Human_SNP_ID_116491569 m1A Human chr2 - 230878695 230878695 230878695 TTGACGGACTCATCCCCACTCCCCAAACTCCAAGCTCCTGCTGGTGGGCTGAAGGCACTGACAGA TTGACGGACTCATCCCCACTCCCCAAACTCCATGCTCCTGCTGGTGGGCTGAAGGCACTGACAGA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:230878601..230879051 32194978 MeRIP-seq:(Medium) rs1365964856 Functional Loss SNV dbSNP153 33..33 33 - - - 97877 RMVar_ID_97877 Human_SNP_ID_116523996 m1A Human chr2 - 231005028 231005019 231005028 TGATGGTGGTGGTGGTGATGATGATGGTGATGATGGTGATGGTGATGATGGTGGTGATGATGGTG TGATGGTGGTGGTGGTGATGATGATGGTGATG_________GTGATGATGGTGGTGATGATGGTG CCATCACCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005000..231005114 26863196 MeRIP-seq:(Medium) rs1559197161 Functional Loss DEL dbSNP153 33..41 33 - - - 97878 RMVar_ID_97878 Human_SNP_ID_116524002 m1A Human chr2 - 231005028 231005025 231005028 TGATGGTGGTGGTGGTGATGATGATGGTGATGATGGTGATGGTGATGATGGTGGTGATGATGGTG TGATGGTGGTGGTGGTGATGATGATGGTGATG___GTGATGGTGATGATGGTGGTGATGATGGTG CCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005000..231005114 26863196 MeRIP-seq:(Medium) rs1222276798 Functional Loss DEL dbSNP153 33..35 33 - - - 97879 RMVar_ID_97879 Human_SNP_ID_116524004 m1A Human chr2 - 231005028 231005028 231005028 TGATGGTGGTGGTGGTGATGATGATGGTGATGATGGTGATGGTGATGATGGTGGTGATGATGGTG TGATGGTGGTGGTGGTGATGATGATGGTGATGGTGGTGATGGTGATGATGGTGGTGATGATGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005000..231005114 26863196 MeRIP-seq:(Medium) rs201702649 Functional Loss SNV dbSNP153 33..33 33 - - - 97880 RMVar_ID_97880 Human_SNP_ID_116524044 m1A Human chr2 - 231005094 231005094 231005094 TGGTGGTGGTGATGATGGTGATGGTGATGAGGATGGTGATGGTGATGATGGTGGTGGTGATGATG TGGTGGTGGTGATGATGGTGATGGTGATGAGGGTGGTGATGGTGATGATGGTGGTGGTGATGATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231005000..231005126 26863196 MeRIP-seq:(Medium) rs1224819656 Functional Loss SNV dbSNP153 33..33 33 - - - 97881 RMVar_ID_97881 Human_SNP_ID_116524054 m1A Human chr2 - 231005115 231005115 231005115 TGGTGGTGGTGGTGATGATGATGGTGGTGGTGATGATGGTGATGGTGATGAGGATGGTGATGGTG TGGTGGTGGTGGTGATGATGATGGTGGTGGTGGTGATGGTGATGGTGATGAGGATGGTGATGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231005021..231005145 26863196 MeRIP-seq:(Medium) rs1322033652 Functional Loss SNV dbSNP153 33..33 33 - - - 97882 RMVar_ID_97882 Human_SNP_ID_116524220 m1A Human chr2 - 231005328 231005325 231005328 TGGTGGTGATGGTGATGATGGTGATGGTGATGATGGTGATGATGATGGTGGTGATGGTGGTGGTG TGGTGGTGATGGTGATGATGGTGATGGTGATG___GTGATGATGATGGTGGTGATGGTGGTGGTG CCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005188..231005387 26863196 MeRIP-seq:(Medium) rs1307881490 Functional Loss DEL dbSNP153 33..35 33 - - - 97883 RMVar_ID_97883 Human_SNP_ID_116524222 m1A Human chr2 - 231005328 231005327 231005328 TGGTGGTGATGGTGATGATGGTGATGGTGATGATGGTGATGATGATGGTGGTGATGGTGGTGGTG TGGTGGTGATGGTGATGATGGTGATGGTGATG_TGGTGATGATGATGGTGGTGATGGTGGTGGTG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005188..231005387 26863196 MeRIP-seq:(Medium) rs1337583775 Functional Loss DEL dbSNP153 33..33 33 - - - 97884 RMVar_ID_97884 Human_SNP_ID_116524225 m1A Human chr2 - 231005328 231005328 231005328 TGGTGGTGATGGTGATGATGGTGATGGTGATGATGGTGATGATGATGGTGGTGATGGTGGTGGTG TGGTGGTGATGGTGATGATGGTGATGGTGATGGTGGTGATGATGATGGTGGTGATGGTGGTGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005188..231005387 26863196 MeRIP-seq:(Medium) rs1176426990 Functional Loss SNV dbSNP153 33..33 33 - - - 97885 RMVar_ID_97885 Human_SNP_ID_116524226 m1A Human chr2 - 231005328 231005328 231005328 TGGTGGTGATGGTGATGATGGTGATGGTGATGATGGTGATGATGATGGTGGTGATGGTGGTGGTG TGGTGGTGATGGTGATGATGGTGATGGTGATGCTGGTGATGATGATGGTGGTGATGGTGGTGGTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231005188..231005387 26863196 MeRIP-seq:(Medium) rs1176426990 Functional Loss SNV dbSNP153 33..33 33 - - - 97886 RMVar_ID_97886 Human_SNP_ID_116532463 m1A Human chr2 + 231037660 231037660 231037660 GGCGTTGGTGGAAGCGGCGGGGGGCCGCGGGCAGGTGCTGCTGGTGGGCGAGCTGTGGGAGCGCG GGCGTTGGTGGAAGCGGCGGGGGGCCGCGGGCCGGTGCTGCTGGTGGGCGAGCTGTGGGAGCGCG A C C2orf72 Ensembl:ENSG00000204128 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:231037527..231037820;chr2:231037537..231037800 26863196 MeRIP-seq:(Medium) rs1194882866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639019,Human_RBP_ID_4622983,Human_RBP_ID_9353945,Human_RBP_ID_9428964,Human_RBP_ID_18462284,Human_RBP_ID_22450952 Human_Splice_Rec_369389 97887 RMVar_ID_97887 Human_SNP_ID_116532521 m1A Human chr2 - 231037832 231037824 231037833 CGCGCCGCCGCCGCCGCCGCCCCCGCCGCCCCAGCCGCCCTCGCCGCCCTCTGCGCCCCGCGCGC CGCGCCGCCGCCGCCGCCGCCCCCGCCGCCC_________TCGCCGCCCTCTGCGCCCCGCGCGC AGGGCGGCTG A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231037736..231037836 26863410 MeRIP-seq:(Medium) rs989906671 Functional Loss DEL dbSNP153 32..40 33 - - - 97888 RMVar_ID_97888 Human_SNP_ID_116532530 m1A Human chr2 - 231037832 231037832 231037832 CGCGCCGCCGCCGCCGCCGCCCCCGCCGCCCCAGCCGCCCTCGCCGCCCTCTGCGCCCCGCGCGC CGCGCCGCCGCCGCCGCCGCCCCCGCCGCCCCCGCCGCCCTCGCCGCCCTCTGCGCCCCGCGCGC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231037736..231037836 26863410 MeRIP-seq:(Medium) rs550300394 Functional Loss SNV dbSNP153 33..33 33 - - - 97889 RMVar_ID_97889 Human_SNP_ID_116537282 m1A Human chr2 - 231056948 231056948 231056948 GCGCAGTGTATCTGTCAGCTCAGGGGCCGCTCAGTTCACCGCGCCTCCTTGCTCCCCGGGTGCGC GCGCAGTGTATCTGTCAGCTCAGGGGCCGCTCGGTTCACCGCGCCTCCTTGCTCCCCGGGTGCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231056876..231057025 26863196 MeRIP-seq:(Medium) rs1288386462 Functional Loss SNV dbSNP153 33..33 33 - - - 97890 RMVar_ID_97890 Human_SNP_ID_116537296 m1A Human chr2 + 231056972 231056972 231056972 CGGTGAACTGAGCGGCCCCTGAGCTGACAGATACACTGCGCAGCTGGAACGGCGAGCGAGCCGAC CGGTGAACTGAGCGGCCCCTGAGCTGACAGATGCACTGCGCAGCTGGAACGGCGAGCGAGCCGAC A G PSMD1 Ensembl:ENSG00000173692 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231056876..231057084 26863196 MeRIP-seq:(Medium) rs943816287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60289,Human_RBP_ID_1584140,Human_RBP_ID_4599317,Human_RBP_ID_8852213,Human_RBP_ID_9296964,Human_RBP_ID_22997086,Human_RBP_ID_23115163,Human_RBP_ID_23119513,Human_RBP_ID_27007677 Human_Splice_Rec_369395,Human_Splice_Rec_369441,Human_Splice_Rec_369481,Human_Splice_Rec_369529,Human_Splice_Rec_369539 RMVar_hsa_circ_113288,RMVar_hsa_circ_207521 97891 RMVar_ID_97891 Human_SNP_ID_116537323 m1A Human chr2 + 231057022 231057022 231057022 GGCGAGCGAGCCGACGGGCGAGTGAGGGGCGCAGCCATGATCACCTCGGCCGGTGAGTGCGGCCC GGCGAGCGAGCCGACGGGCGAGTGAGGGGCGCGGCCATGATCACCTCGGCCGGTGAGTGCGGCCC A G PSMD1 Ensembl:ENSG00000173692 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:231056926..231057050 26863410 MeRIP-seq:(Medium) rs1021252923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243190,Human_RBP_ID_829405,Human_RBP_ID_4623904,Human_RBP_ID_8851706,Human_RBP_ID_9388067,Human_RBP_ID_18443172,Human_RBP_ID_19098870,Human_RBP_ID_22997537,Human_RBP_ID_23115163,Human_RBP_ID_23119513 Human_Splice_Rec_369395,Human_Splice_Rec_369441,Human_Splice_Rec_369481,Human_Splice_Rec_369529,Human_Splice_Rec_369539 Human_miRNA_ID_2276150 RMVar_hsa_circ_113288,RMVar_hsa_circ_207521 97892 RMVar_ID_97892 Human_SNP_ID_116562587 m1A Human chr2 - 231165853 231165853 231165853 TTTCTCTGCCTCATCCTATAAAATAAAATTTAAAAAAAGTTCAACAGAAGTTCATTTCTGTTCCA TTTCTCTGCCTCATCCTATAAAATAAAATTTATAAAAAGTTCAACAGAAGTTCATTTCTGTTCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231165851..231165925 26863196 MeRIP-seq:(Medium) rs1292149054 Functional Loss SNV dbSNP153 33..33 33 - - - 97893 RMVar_ID_97893 Human_SNP_ID_116562588 m1A Human chr2 - 231165853 231165853 231165853 TTTCTCTGCCTCATCCTATAAAATAAAATTTAAAAAAAGTTCAACAGAAGTTCATTTCTGTTCCA TTTCTCTGCCTCATCCTATAAAATAAAATTTACAAAAAGTTCAACAGAAGTTCATTTCTGTTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231165851..231165925 26863196 MeRIP-seq:(Medium) rs1292149054 Functional Loss SNV dbSNP153 33..33 33 - - - 97894 RMVar_ID_97894 Human_SNP_ID_116562633 m1A Human chr2 + 231166013 231166013 231166013 CATGCCGGAGACCTGTAGATACCAGCCTTTCAAACCAGTAAGTTACCAGTGACTCTTAGCTGTAT CATGCCGGAGACCTGTAGATACCAGCCTTTCAGACCAGTAAGTTACCAGTGACTCTTAGCTGTAT A G PSMD1 Ensembl:ENSG00000173692 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:231165248..231170515 32194978 MeRIP-seq:(Medium) rs1400095124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9385573,Human_RBP_ID_13793901,Human_RBP_ID_17658748,Human_RBP_ID_24546565,Human_RBP_ID_26340332,Human_RBP_ID_27818037 Human_Splice_Rec_369437,Human_Splice_Rec_369525,Human_Splice_Rec_369581,Human_Splice_Rec_369625 RMVar_hsa_circ_101974,RMVar_hsa_circ_207528,RMVar_hsa_circ_369372,RMVar_hsa_circ_207533,RMVar_hsa_circ_342332,RMVar_hsa_circ_373370,RMVar_hsa_circ_207543,RMVar_hsa_circ_207545,RMVar_hsa_circ_359209 97895 RMVar_ID_97895 Human_SNP_ID_116570523 m1A Human chr2 - 231198679 231198679 231198679 GGGACGCGCTTACCTGCTGCTCGGCCGCGGACACTCGCGCTATCCCAGCCCGGCCGCCACCTCCG GGGACGCGCTTACCTGCTGCTCGGCCGCGGACCCTCGCGCTATCCCAGCCCGGCCGCCACCTCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231198673..231198855 26863196 MeRIP-seq:(Medium) rs191013678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18755692 97896 RMVar_ID_97896 Human_SNP_ID_116635341 m1A Human chr2 - 231455228 231455228 231455228 AGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGACCACAAGCCACAAGGAAAGAAGACGAAGTTTG AGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGCCCACAAGCCACAAGGAAAGAAGACGAAGTTTG T G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:231455126..231455418 26863410 MeRIP-seq:(Medium) rs750135695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545701,Human_RBP_ID_829693,Human_RBP_ID_1068038,Human_RBP_ID_1584169,Human_RBP_ID_1912493,Human_RBP_ID_4599413,Human_RBP_ID_6895021,Human_RBP_ID_8513761,Human_RBP_ID_9385581,Human_RBP_ID_17658753,Human_RBP_ID_22077436,Human_RBP_ID_22452012,Human_RBP_ID_22814964,Human_RBP_ID_22990199,Human_RBP_ID_24488475,Human_RBP_ID_24546238,Human_RBP_ID_25586856,Human_RBP_ID_26340333,Human_RBP_ID_26480447,Human_RBP_ID_27007737,Human_RBP_ID_27287441,Human_RBP_ID_27478229 Human_Splice_Rec_369926,Human_Splice_Rec_369950 Human_miRNA_ID_2014995 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 97897 RMVar_ID_97897 Human_SNP_ID_116635351 m1A Human chr2 - 231455244 231455238 231455244 CTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGACCACAAGCCACAAGGA CTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGC______GGAGGAGGTGACCACAAGCCACAAGGA CTCCTCT C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:231454975..231456725 32194978 MeRIP-seq:(Medium) rs1348613998 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_242380,Human_RBP_ID_545701,Human_RBP_ID_774974,Human_RBP_ID_829693,Human_RBP_ID_922594,Human_RBP_ID_1068038,Human_RBP_ID_4599413,Human_RBP_ID_6895021,Human_RBP_ID_17657922,Human_RBP_ID_22076871,Human_RBP_ID_22452012,Human_RBP_ID_23132777,Human_RBP_ID_24546238,Human_RBP_ID_26340333,Human_RBP_ID_27819358 Human_Splice_Rec_369926,Human_Splice_Rec_369950 Human_miRNA_ID_2014995 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 97898 RMVar_ID_97898 Human_SNP_ID_116635357 m1A Human chr2 - 231455251 231455251 231455251 TGCCTTCCTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGACCACAAGCC TGCCTTCCTCCTGTAGGGCGAGGAGGCTTCCGTGGAGGCAGAGGAGGAGGAGGTGACCACAAGCC T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231455151..231455422 26863410 MeRIP-seq:(Medium) rs551909257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242380,Human_RBP_ID_545701,Human_RBP_ID_774974,Human_RBP_ID_829693,Human_RBP_ID_922594,Human_RBP_ID_1068038,Human_RBP_ID_4599416,Human_RBP_ID_6895022,Human_RBP_ID_9385582,Human_RBP_ID_17657922,Human_RBP_ID_22076871,Human_RBP_ID_22452012,Human_RBP_ID_23132778,Human_RBP_ID_24546567,Human_RBP_ID_26340333,Human_RBP_ID_27819358 Human_Splice_Rec_369926,Human_Splice_Rec_369950 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 97899 RMVar_ID_97899 Human_SNP_ID_116635358 m1A Human chr2 - 231455251 231455251 231455251 TGCCTTCCTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGACCACAAGCC TGCCTTCCTCCTGTAGGGCGAGGAGGCTTCCGGGGAGGCAGAGGAGGAGGAGGTGACCACAAGCC T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231455151..231455422 26863410 MeRIP-seq:(Medium) rs551909257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242380,Human_RBP_ID_545701,Human_RBP_ID_774974,Human_RBP_ID_829693,Human_RBP_ID_922594,Human_RBP_ID_1068038,Human_RBP_ID_4599416,Human_RBP_ID_6895022,Human_RBP_ID_9385582,Human_RBP_ID_17657922,Human_RBP_ID_22076871,Human_RBP_ID_22452012,Human_RBP_ID_23132778,Human_RBP_ID_24546567,Human_RBP_ID_26340333,Human_RBP_ID_27819358 Human_Splice_Rec_369926,Human_Splice_Rec_369950 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 97900 RMVar_ID_97900 Human_SNP_ID_116635365 m1A Human chr2 - 231455263 231455263 231455263 TTAACAGTGTCTTGCCTTCCTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGG TTAACAGTGTCTTGCCTTCCTCCTGTAGGGCGGGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:231455226..231455562 26863196 MeRIP-seq:(Medium) rs1200887351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56983,Human_RBP_ID_242380,Human_RBP_ID_774974,Human_RBP_ID_829693,Human_RBP_ID_922594,Human_RBP_ID_1068038,Human_RBP_ID_4599417,Human_RBP_ID_6895022,Human_RBP_ID_9385582,Human_RBP_ID_17657922,Human_RBP_ID_22077436,Human_RBP_ID_22452012,Human_RBP_ID_23119349,Human_RBP_ID_23132778,Human_RBP_ID_24546567,Human_RBP_ID_26340333,Human_RBP_ID_27819358 Human_Splice_Rec_369926,Human_Splice_Rec_369950 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 97901 RMVar_ID_97901 Human_SNP_ID_116635454 m1A Human chr2 - 231455438 231455414 231455438 TTTGGAGGACGAGGTGGTGGTAGAGGAGGCCGAGGAGGATTTGGTGGCAGAGGCCGGGGAGGCTT TTTGGAGGACGAGGTGGTGGTAGAGGAGGCCG________________________GGGAGGCTT CCGGCCTCTGCCACCAAATCCTCCT C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:231455201..231455600 26863196 MeRIP-seq:(Medium) rs1486884325 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_242112,Human_RBP_ID_545704,Human_RBP_ID_774976,Human_RBP_ID_828392,Human_RBP_ID_1022244,Human_RBP_ID_1067771,Human_RBP_ID_1584170,Human_RBP_ID_3617987,Human_RBP_ID_6895025,Human_RBP_ID_8513762,Human_RBP_ID_8846300,Human_RBP_ID_9296972,Human_RBP_ID_9353841,Human_RBP_ID_17658270,Human_RBP_ID_17952169,Human_RBP_ID_22450954,Human_RBP_ID_22814965,Human_RBP_ID_22997540,Human_RBP_ID_23132779,Human_RBP_ID_23856606,Human_RBP_ID_24553310,Human_RBP_ID_25586857,Human_RBP_ID_26340337,Human_RBP_ID_27007740 Human_Splice_Rec_369925,Human_Splice_Rec_369949 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_377381,RMVar_hsa_circ_207584 97902 RMVar_ID_97902 Human_SNP_ID_116635466 m1A Human chr2 - 231455444 231455441 231455444 GGCGGCTTTGGAGGACGAGGTGGTGGTAGAGGAGGCCGAGGAGGATTTGGTGGCAGAGGCCGGGG GGCGGCTTTGGAGGACGAGGTGGTGGTAGAGG___CCGAGGAGGATTTGGTGGCAGAGGCCGGGG GCCT G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231455401..231455500 26863196 MeRIP-seq:(Medium) rs780620829 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_242112,Human_RBP_ID_545704,Human_RBP_ID_774976,Human_RBP_ID_828392,Human_RBP_ID_1022244,Human_RBP_ID_1067771,Human_RBP_ID_1584170,Human_RBP_ID_3617987,Human_RBP_ID_6895025,Human_RBP_ID_8513762,Human_RBP_ID_8846300,Human_RBP_ID_9296972,Human_RBP_ID_9353841,Human_RBP_ID_17658270,Human_RBP_ID_17952169,Human_RBP_ID_22450104,Human_RBP_ID_22814965,Human_RBP_ID_22998805,Human_RBP_ID_23132779,Human_RBP_ID_23856606,Human_RBP_ID_24488476,Human_RBP_ID_24553310,Human_RBP_ID_25586857,Human_RBP_ID_26338818,Human_RBP_ID_27007740 Human_Splice_Rec_369925,Human_Splice_Rec_369949 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_377381,RMVar_hsa_circ_207584 97903 RMVar_ID_97903 Human_SNP_ID_116635470 m1A Human chr2 - 231455444 231455444 231455444 GGCGGCTTTGGAGGACGAGGTGGTGGTAGAGGAGGCCGAGGAGGATTTGGTGGCAGAGGCCGGGG GGCGGCTTTGGAGGACGAGGTGGTGGTAGAGGCGGCCGAGGAGGATTTGGTGGCAGAGGCCGGGG T G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231455401..231455500 26863196 MeRIP-seq:(Medium) rs754163466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242112,Human_RBP_ID_545704,Human_RBP_ID_774976,Human_RBP_ID_828392,Human_RBP_ID_1022244,Human_RBP_ID_1067771,Human_RBP_ID_1584170,Human_RBP_ID_3617987,Human_RBP_ID_6895025,Human_RBP_ID_8513762,Human_RBP_ID_8846300,Human_RBP_ID_9296972,Human_RBP_ID_9353841,Human_RBP_ID_17658270,Human_RBP_ID_17952169,Human_RBP_ID_22450104,Human_RBP_ID_22814965,Human_RBP_ID_22998805,Human_RBP_ID_23132779,Human_RBP_ID_23856606,Human_RBP_ID_24488476,Human_RBP_ID_24553310,Human_RBP_ID_25586857,Human_RBP_ID_26338818,Human_RBP_ID_27007740 Human_Splice_Rec_369925,Human_Splice_Rec_369949 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_377381,RMVar_hsa_circ_207584 97904 RMVar_ID_97904 Human_SNP_ID_116635478 m1A Human chr2 + 231455470 231455470 231455470 TCGGCCTCCTCTACCACCACCTCGTCCTCCAAAGCCGCCTCTGCCTCCACCACGACCCCCGAAGC TCGGCCTCCTCTACCACCACCTCGTCCTCCAAGGCCGCCTCTGCCTCCACCACGACCCCCGAAGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:231455201..231455625 26863196 MeRIP-seq:(Medium) rs776324322 Functional Loss SNV dbSNP153 33..33 33 - - - 97905 RMVar_ID_97905 Human_SNP_ID_116635962 m1A Human chr2 - 231456680 231456680 231456680 TCCTGTAATAAAAGGGAAATTGAGGGCAGAGCAATCAGGCTGGAGTTGCAAGGACCCAGGGGATC TCCTGTAATAAAAGGGAAATTGAGGGCAGAGCTATCAGGCTGGAGTTGCAAGGACCCAGGGGATC T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:231456594..231456679;chr2:231456595..231456714 26863196 MeRIP-seq:(Medium) rs748660793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56987,Human_RBP_ID_545723,Human_RBP_ID_829696,Human_RBP_ID_1022254,Human_RBP_ID_1584190,Human_RBP_ID_1912506,Human_RBP_ID_2626988,Human_RBP_ID_3617998,Human_RBP_ID_4630892,Human_RBP_ID_6895048,Human_RBP_ID_8513783,Human_RBP_ID_8846321,Human_RBP_ID_9103855,Human_RBP_ID_9385594,Human_RBP_ID_13794620,Human_RBP_ID_17275377,Human_RBP_ID_17390546,Human_RBP_ID_17506463,Human_RBP_ID_22076873,Human_RBP_ID_22814974,Human_RBP_ID_26338824,Human_RBP_ID_27007752,Human_RBP_ID_27287457,Human_RBP_ID_27693580 Human_Splice_Rec_369920,Human_Splice_Rec_369921,Human_Splice_Rec_369944,Human_Splice_Rec_369945,Human_Splice_Rec_369958,Human_Splice_Rec_369959,Human_Splice_Rec_369964,Human_Splice_Rec_369965 Human_miRNA_ID_2394515,Human_miRNA_ID_2906497,Human_miRNA_ID_2972527,Human_miRNA_ID_3005713,Human_miRNA_ID_3025328 RMVar_hsa_circ_69694,RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_87001,RMVar_hsa_circ_120922,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207590,RMVar_hsa_circ_75733,RMVar_hsa_circ_207591,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587 97906 RMVar_ID_97906 Human_SNP_ID_116636342 m1A Human chr2 - 231457734 231457734 231457734 GCAGAGAAAACCTTTGAAGAAAAGCAGGGAACAGAGATCGATGGGCGATCTATTTCCCTGTACTA GCAGAGAAAACCTTTGAAGAAAAGCAGGGAACTGAGATCGATGGGCGATCTATTTCCCTGTACTA T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231457683..231457752 26863196 MeRIP-seq:(Medium) rs757879474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545736,Human_RBP_ID_1584199,Human_RBP_ID_1912520,Human_RBP_ID_2627008,Human_RBP_ID_3618002,Human_RBP_ID_4599458,Human_RBP_ID_6895062,Human_RBP_ID_8513791,Human_RBP_ID_8846329,Human_RBP_ID_9103858,Human_RBP_ID_9385603,Human_RBP_ID_13794648,Human_RBP_ID_17964355,Human_RBP_ID_18315308,Human_RBP_ID_18544609,Human_RBP_ID_18755746,Human_RBP_ID_20536010,Human_RBP_ID_22006104,Human_RBP_ID_22248571,Human_RBP_ID_22814980,Human_RBP_ID_22998821,Human_RBP_ID_23856644,Human_RBP_ID_26338830,Human_RBP_ID_27007763,Human_RBP_ID_27287465,Human_RBP_ID_27818044 Human_Splice_Rec_369916,Human_Splice_Rec_369917,Human_Splice_Rec_369940,Human_Splice_Rec_369941,Human_Splice_Rec_369952,Human_Splice_Rec_369953,Human_Splice_Rec_369976 Human_miRNA_ID_2958652 RMVar_hsa_circ_61891,RMVar_hsa_circ_69694,RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207590,RMVar_hsa_circ_75733,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587 97907 RMVar_ID_97907 Human_SNP_ID_116636345 m1A Human chr2 - 231457737 231457737 231457737 GATGCAGAGAAAACCTTTGAAGAAAAGCAGGGAACAGAGATCGATGGGCGATCTATTTCCCTGTA GATGCAGAGAAAACCTTTGAAGAAAAGCAGGGTACAGAGATCGATGGGCGATCTATTTCCCTGTA T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231457688..231457813 26863196 MeRIP-seq:(Medium) rs1279133334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545736,Human_RBP_ID_1584199,Human_RBP_ID_1912520,Human_RBP_ID_2627008,Human_RBP_ID_3618003,Human_RBP_ID_4599458,Human_RBP_ID_6895062,Human_RBP_ID_8513791,Human_RBP_ID_8846329,Human_RBP_ID_9103858,Human_RBP_ID_9385603,Human_RBP_ID_13794652,Human_RBP_ID_17964355,Human_RBP_ID_18315308,Human_RBP_ID_18533501,Human_RBP_ID_18544609,Human_RBP_ID_18755746,Human_RBP_ID_20536010,Human_RBP_ID_22006104,Human_RBP_ID_22248571,Human_RBP_ID_22814980,Human_RBP_ID_22998821,Human_RBP_ID_23856644,Human_RBP_ID_26340352,Human_RBP_ID_27007763,Human_RBP_ID_27287465,Human_RBP_ID_27818044 Human_Splice_Rec_369916,Human_Splice_Rec_369917,Human_Splice_Rec_369940,Human_Splice_Rec_369941,Human_Splice_Rec_369952,Human_Splice_Rec_369953,Human_Splice_Rec_369976 Human_miRNA_ID_2958652 RMVar_hsa_circ_61891,RMVar_hsa_circ_69694,RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207590,RMVar_hsa_circ_75733,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587 97908 RMVar_ID_97908 Human_SNP_ID_116637457 m1A Human chr2 - 231460703 231460694 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGA_________GGAGGAGGAAGAAGAGGAGGAGGA CTCATCATCT C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs780927712 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97909 RMVar_ID_97909 Human_SNP_ID_116637465 m1A Human chr2 - 231460703 231460697 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGA______TGAGGAGGAGGAAGAAGAGGAGGAGGA ATCATCT A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs770891540 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97910 RMVar_ID_97910 Human_SNP_ID_116637470 m1A Human chr2 - 231460703 231460700 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGA___TGATGAGGAGGAGGAAGAAGAGGAGGAGGA ATCT A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs746082903 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97911 RMVar_ID_97911 Human_SNP_ID_116637477 m1A Human chr2 - 231460703 231460703 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGATGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs199689485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97912 RMVar_ID_97912 Human_SNP_ID_116637478 m1A Human chr2 - 231460703 231460703 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGAGGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs199689485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97913 RMVar_ID_97913 Human_SNP_ID_116637546 m1A Human chr2 - 231460752 231460752 231460752 GGCTGAGGATGAAGATGAAGAAGAGGATGATGAGGACGAGGATGACGACGACGACGAAGATGATG GGCTGAGGATGAAGATGAAGAAGAGGATGATGGGGACGAGGATGACGACGACGACGAAGATGATG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:231460551..231460875 26863196 MeRIP-seq:(Medium) rs758559474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_545751,Human_RBP_ID_774983,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1299877,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627049,Human_RBP_ID_3618016,Human_RBP_ID_4599478,Human_RBP_ID_5194520,Human_RBP_ID_5501793,Human_RBP_ID_5589079,Human_RBP_ID_6895102,Human_RBP_ID_8257488,Human_RBP_ID_8513813,Human_RBP_ID_8846342,Human_RBP_ID_9385635,Human_RBP_ID_9975863,Human_RBP_ID_13794780,Human_RBP_ID_17275388,Human_RBP_ID_17390555,Human_RBP_ID_17506476,Human_RBP_ID_18443191,Human_RBP_ID_18533503,Human_RBP_ID_22076883,Human_RBP_ID_22743086,Human_RBP_ID_22996919,Human_RBP_ID_23115003,Human_RBP_ID_23119355,Human_RBP_ID_23856671,Human_RBP_ID_24545951,Human_RBP_ID_26338841,Human_RBP_ID_27478262,Human_RBP_ID_27818061 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97914 RMVar_ID_97914 Human_SNP_ID_116637551 m1A Human chr2 - 231460758 231460758 231460758 GAACGTGGCTGAGGATGAAGATGAAGAAGAGGATGATGAGGACGAGGATGACGACGACGACGAAG GAACGTGGCTGAGGATGAAGATGAAGAAGAGGTTGATGAGGACGAGGATGACGACGACGACGAAG T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231460554..231460816 26863410 MeRIP-seq:(Medium) rs751558153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_774983,Human_RBP_ID_829701,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627049,Human_RBP_ID_3618016,Human_RBP_ID_4599478,Human_RBP_ID_5194520,Human_RBP_ID_5501794,Human_RBP_ID_5589079,Human_RBP_ID_6895102,Human_RBP_ID_8107524,Human_RBP_ID_8257488,Human_RBP_ID_8513813,Human_RBP_ID_8846342,Human_RBP_ID_9385635,Human_RBP_ID_9975863,Human_RBP_ID_13794781,Human_RBP_ID_17275388,Human_RBP_ID_17390555,Human_RBP_ID_17506476,Human_RBP_ID_17952195,Human_RBP_ID_18443191,Human_RBP_ID_18533503,Human_RBP_ID_22076883,Human_RBP_ID_22248589,Human_RBP_ID_22743086,Human_RBP_ID_22996919,Human_RBP_ID_23115003,Human_RBP_ID_23119355,Human_RBP_ID_23856671,Human_RBP_ID_24545951,Human_RBP_ID_26338841,Human_RBP_ID_27478262,Human_RBP_ID_27563645,Human_RBP_ID_27818061 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97915 RMVar_ID_97915 Human_SNP_ID_116637552 m1A Human chr2 - 231460758 231460758 231460758 GAACGTGGCTGAGGATGAAGATGAAGAAGAGGATGATGAGGACGAGGATGACGACGACGACGAAG GAACGTGGCTGAGGATGAAGATGAAGAAGAGGGTGATGAGGACGAGGATGACGACGACGACGAAG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231460554..231460816 26863410 MeRIP-seq:(Medium) rs751558153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_774983,Human_RBP_ID_829701,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627049,Human_RBP_ID_3618016,Human_RBP_ID_4599478,Human_RBP_ID_5194520,Human_RBP_ID_5501794,Human_RBP_ID_5589079,Human_RBP_ID_6895102,Human_RBP_ID_8107524,Human_RBP_ID_8257488,Human_RBP_ID_8513813,Human_RBP_ID_8846342,Human_RBP_ID_9385635,Human_RBP_ID_9975863,Human_RBP_ID_13794781,Human_RBP_ID_17275388,Human_RBP_ID_17390555,Human_RBP_ID_17506476,Human_RBP_ID_17952195,Human_RBP_ID_18443191,Human_RBP_ID_18533503,Human_RBP_ID_22076883,Human_RBP_ID_22248589,Human_RBP_ID_22743086,Human_RBP_ID_22996919,Human_RBP_ID_23115003,Human_RBP_ID_23119355,Human_RBP_ID_23856671,Human_RBP_ID_24545951,Human_RBP_ID_26338841,Human_RBP_ID_27478262,Human_RBP_ID_27563645,Human_RBP_ID_27818061 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 97916 RMVar_ID_97916 Human_SNP_ID_116637923 m1A Human chr2 + 231461644 231461639 231461645 CAGCAGCTGCTGCTTTCATCGCTGCTGGTTCAATTTCATCTTCATCCTCATCCTCGTCCTCGTCA CAGCAGCTGCTGCTTTCATCGCTGCTGG______TTCATCTTCATCCTCATCCTCGTCCTCGTCA GTTCAAT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:231461544..231461763 26863196 MeRIP-seq:(Medium) rs1300956268 Functional Loss DEL dbSNP153 29..34 33 - - - 97917 RMVar_ID_97917 Human_SNP_ID_116637970 m1A Human chr2 - 231461707 231461707 231461707 GAATGCCAAGAAGGAAGACAGTGATGAAGAGGAGGATGATGACAGTGAGGAGGATGAGGAGGATG GAATGCCAAGAAGGAAGACAGTGATGAAGAGGGGGATGATGACAGTGAGGAGGATGAGGAGGATG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:231461525..231461800 26863196 MeRIP-seq:(Medium) rs1172529806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545754,Human_RBP_ID_1022274,Human_RBP_ID_1584242,Human_RBP_ID_1912555,Human_RBP_ID_2627063,Human_RBP_ID_3618020,Human_RBP_ID_4599488,Human_RBP_ID_5589083,Human_RBP_ID_6895114,Human_RBP_ID_8257495,Human_RBP_ID_8846353,Human_RBP_ID_13794816,Human_RBP_ID_17390560,Human_RBP_ID_17506483,Human_RBP_ID_17952202,Human_RBP_ID_18412829,Human_RBP_ID_18443194,Human_RBP_ID_18533510,Human_RBP_ID_18755785,Human_RBP_ID_22076887,Human_RBP_ID_22505225,Human_RBP_ID_22743089,Human_RBP_ID_22996920,Human_RBP_ID_23115082,Human_RBP_ID_23119357,Human_RBP_ID_23856678,Human_RBP_ID_24545958,Human_RBP_ID_26338846,Human_RBP_ID_27007806,Human_RBP_ID_27818068 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_207593 97918 RMVar_ID_97918 Human_SNP_ID_116638520 m1A Human chr2 - 231463216 231463214 231463217 AGATGAGGAAATGTCAGAAGATGAAGAAGATGATAGCAGTGGAGAAGAGGTAATTTTATCCAACT AGATGAGGAAATGTCAGAAGATGAAGAAGAT___AGCAGTGGAGAAGAGGTAATTTTATCCAACT TATC T NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231463201..231463623 26863196 MeRIP-seq:(Medium) rs774868867 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_206299,Human_RBP_ID_242390,Human_RBP_ID_830862,Human_RBP_ID_920618,Human_RBP_ID_1584253,Human_RBP_ID_1912563,Human_RBP_ID_2627080,Human_RBP_ID_3618027,Human_RBP_ID_4630939,Human_RBP_ID_5196444,Human_RBP_ID_5589084,Human_RBP_ID_5651992,Human_RBP_ID_6895136,Human_RBP_ID_8234577,Human_RBP_ID_8257497,Human_RBP_ID_8513830,Human_RBP_ID_9330834,Human_RBP_ID_9385663,Human_RBP_ID_9975871,Human_RBP_ID_13794867,Human_RBP_ID_17506489,Human_RBP_ID_18412834,Human_RBP_ID_18544621,Human_RBP_ID_18755795,Human_RBP_ID_22078393,Human_RBP_ID_22505227,Human_RBP_ID_22815007,Human_RBP_ID_22996924,Human_RBP_ID_23115165,Human_RBP_ID_23119360,Human_RBP_ID_23856690,Human_RBP_ID_24545966,Human_RBP_ID_26338851,Human_RBP_ID_27007815,Human_RBP_ID_27478280,Human_RBP_ID_27818073 Human_Splice_Rec_369903,Human_Splice_Rec_369929,Human_Splice_Rec_369979,Human_Splice_Rec_369983,Human_Splice_Rec_369987,Human_Splice_Rec_369991 Human_miRNA_ID_2967658 RMVar_hsa_circ_89925,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_207588,RMVar_hsa_circ_207587,RMVar_hsa_circ_207594,RMVar_hsa_circ_98924 97919 RMVar_ID_97919 Human_SNP_ID_116638563 m1A Human chr2 - 231463314 231463314 231463314 GGTGTAATGATCTATTTGTGTCCATTTTAGGCAGGTAAAAATCAAGGTGACCCCAAGAAAATGGC GGTGTAATGATCTATTTGTGTCCATTTTAGGCTGGTAAAAATCAAGGTGACCCCAAGAAAATGGC T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr2:231463151..231463366;chr2:231463226..231463420;chr2:231463226..231463419;chr2:231463226..231463325;chr2:231463163..231463623;chr2:231463251..231463325 26863196,32194978 MeRIP-seq:(Medium) rs770870458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830863,Human_RBP_ID_2627087,Human_RBP_ID_5528268,Human_RBP_ID_9385669,Human_RBP_ID_18412834,Human_RBP_ID_18544621,Human_RBP_ID_24545969,Human_RBP_ID_26338852,Human_RBP_ID_27819399 Human_Splice_Rec_369902,Human_Splice_Rec_369928,Human_Splice_Rec_369978,Human_Splice_Rec_369982,Human_Splice_Rec_369986,Human_Splice_Rec_369990,Human_Splice_Rec_369994 Human_miRNA_ID_2277667 RMVar_hsa_circ_89925,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_207588,RMVar_hsa_circ_207587,RMVar_hsa_circ_207594,RMVar_hsa_circ_98924 97920 RMVar_ID_97920 Human_SNP_ID_116651220 m1A Human chr2 - 231514083 231514083 231514083 TCTGACTGGCGAAGTAAAGGTACTTGAATTGCAGGTACTGTTTTTGGCCCTTTGTCCCCTGTATT TCTGACTGGCGAAGTAAAGGTACTTGAATTGCGGGTACTGTTTTTGGCCCTTTGTCCCCTGTATT T C LINC00471 Ensembl:ENSG00000181798 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231514078..231514310 26863196 MeRIP-seq:(Medium) rs1207878338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_369999 97921 RMVar_ID_97921 Human_SNP_ID_116668040 m1A Human chr2 + 231578912 231578912 231578912 TTATTGTCATCACTATCATCATCATCATCACCATCACCATCACCATCATCATCATCATCACCATC TTATTGTCATCACTATCATCATCATCATCACCGTCACCATCACCATCATCATCATCATCACCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231578908..231578981 26863196 MeRIP-seq:(Medium) rs1204350091 Functional Loss SNV dbSNP153 33..33 33 - - - 97922 RMVar_ID_97922 Human_SNP_ID_116704405 m1A Human chr2 - 231708575 231708575 231708575 GCGCGCGGCGGAGGCGGCTGCGGCGAGCAAGGAGGCGGATGAGGAACAATGCAAAGATGGCTTTT GCGCGCGGCGGAGGCGGCTGCGGCGAGCAAGGGGGCGGATGAGGAACAATGCAAAGATGGCTTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:231708514..231708625;chr2:231708526..231708684;chr2:231708526..231708625;chr2:231708514..231708628;chr2:231708526..231708640 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1016296990 Functional Loss SNV dbSNP153 33..33 33 - - - 97923 RMVar_ID_97923 Human_SNP_ID_116704406 m1A Human chr2 - 231708575 231708575 231708575 GCGCGCGGCGGAGGCGGCTGCGGCGAGCAAGGAGGCGGATGAGGAACAATGCAAAGATGGCTTTT GCGCGCGGCGGAGGCGGCTGCGGCGAGCAAGGCGGCGGATGAGGAACAATGCAAAGATGGCTTTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:231708514..231708625;chr2:231708526..231708684;chr2:231708526..231708625;chr2:231708514..231708628;chr2:231708526..231708640 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1016296990 Functional Loss SNV dbSNP153 33..33 33 - - - 97924 RMVar_ID_97924 Human_SNP_ID_116704459 m1A Human chr2 + 231708625 231708625 231708625 GCCTCCGCCGCGCGCCTCCTCCGCCGCCGCGGACTCCGGCAGCTTTATCGCCAGAGTCCCTGAAC GCCTCCGCCGCGCGCCTCCTCCGCCGCCGCGGCCTCCGGCAGCTTTATCGCCAGAGTCCCTGAAC A C PTMA Ensembl:ENSG00000187514 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:231708526..231708714 26863410 MeRIP-seq:(Medium) rs998899911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2240391,Human_miRNA_ID_2405413,Human_miRNA_ID_2408408,Human_miRNA_ID_2411399,Human_miRNA_ID_2414379,Human_miRNA_ID_2622888,Human_miRNA_ID_3104613 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_75964,RMVar_hsa_circ_207599,RMVar_hsa_circ_207597 97925 RMVar_ID_97925 Human_SNP_ID_116704802 m1A Human chr2 - 231709158 231709158 231709158 GCCGCCACTTCCCGCGGCCGGCCCGCGCCCCAACACGCGCCCCCCAGCACTTCCGATTCCCAACG GCCGCCACTTCCCGCGGCCGGCCCGCGCCCCAGCACGCGCCCCCCAGCACTTCCGATTCCCAACG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:231709155..231709280 32194978 MeRIP-seq:(Medium) rs574163623 Functional Loss SNV dbSNP153 33..33 33 - - - 97926 RMVar_ID_97926 Human_SNP_ID_116704915 m1A Human chr2 - 231709357 231709357 231709357 CCCACCCCCGCCTCCCAGAGCGCCCAAAGCGGATAAGCCCGTCACACCTCCGCCGGGACGGCCGA CCCACCCCCGCCTCCCAGAGCGCCCAAAGCGGGTAAGCCCGTCACACCTCCGCCGGGACGGCCGA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:231709351..231709575 26863196 MeRIP-seq:(Medium) rs1473456524 Functional Loss SNV dbSNP153 33..33 33 - - - 97927 RMVar_ID_97927 Human_SNP_ID_116705297 m1A Human chr2 - 231710066 231710065 231710066 CGGGCTACTACTCATCGCCCTCGCGGGAAGTCACCTTTTGGTGCTTCGGAGAAAATCGAACAGCC CGGGCTACTACTCATCGCCCTCGCGGGAAGTC_CCTTTTGGTGCTTCGGAGAAAATCGAACAGCC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:231710064..231710189 26863196 MeRIP-seq:(Medium) rs1241508111 Functional Loss DEL dbSNP153 33..33 33 - - - 97928 RMVar_ID_97928 Human_SNP_ID_116705605 m1A Human chr2 + 231710516 231710516 231710516 GCGGAGCGGGGCGGGCCGGACTGAGAGGGCCGACAGGTGGCCCGGAGCCGCTCGCCGGACAGCGG GCGGAGCGGGGCGGGCCGGACTGAGAGGGCCGCCAGGTGGCCCGGAGCCGCTCGCCGGACAGCGG A C PTMA Ensembl:ENSG00000187514 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231710509..231711166 26863196 MeRIP-seq:(Medium) rs1162872640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638298,Human_RBP_ID_5118179,Human_RBP_ID_5196146,Human_RBP_ID_5378986,Human_RBP_ID_8200833,Human_RBP_ID_8728590,Human_RBP_ID_18422510,Human_RBP_ID_18462714,Human_RBP_ID_22721166 Human_Splice_Rec_370083 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_207599 97929 RMVar_ID_97929 Human_SNP_ID_116705606 m1A Human chr2 + 231710516 231710516 231710516 GCGGAGCGGGGCGGGCCGGACTGAGAGGGCCGACAGGTGGCCCGGAGCCGCTCGCCGGACAGCGG GCGGAGCGGGGCGGGCCGGACTGAGAGGGCCGGCAGGTGGCCCGGAGCCGCTCGCCGGACAGCGG A G PTMA Ensembl:ENSG00000187514 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231710509..231711166 26863196 MeRIP-seq:(Medium) rs1162872640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638298,Human_RBP_ID_5118179,Human_RBP_ID_5196146,Human_RBP_ID_5378986,Human_RBP_ID_8200833,Human_RBP_ID_8728590,Human_RBP_ID_18422510,Human_RBP_ID_18462714,Human_RBP_ID_22721166 Human_Splice_Rec_370083 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_207599 97930 RMVar_ID_97930 Human_SNP_ID_116706093 m1A Human chr2 - 231711416 231711416 231711416 CAGGGCTCAGGAGCAAAGCAGACACTCACAGCATTCCCGTTAGCAGGGGCGTCTCTTCCATTTTC CAGGGCTCAGGAGCAAAGCAGACACTCACAGCGTTCCCGTTAGCAGGGGCGTCTCTTCCATTTTC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:231711314..231711475 26863410 MeRIP-seq:(Medium) rs1559287952 Functional Loss SNV dbSNP153 33..33 33 - - - 97931 RMVar_ID_97931 Human_SNP_ID_116706095 m1A Human chr2 - 231711421 231711421 231711421 GCTGCCAGGGCTCAGGAGCAAAGCAGACACTCACAGCATTCCCGTTAGCAGGGGCGTCTCTTCCA GCTGCCAGGGCTCAGGAGCAAAGCAGACACTCTCAGCATTCCCGTTAGCAGGGGCGTCTCTTCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Normoxia chr2:231711320..231711469;chr2:231711376..231711425;chr2:231711277..231711504;chr2:231711294..231711472;chr2:231711314..231711464;chr2:231711326..231711425 26863196,26863410,26863196,26863196,32194978 MeRIP-seq:(Medium) rs112973213 Functional Loss SNV dbSNP153 33..33 33 - - - 97932 RMVar_ID_97932 Human_SNP_ID_116706330 m1A Human chr2 + 231711936 231711927 231711936 GGAGCAGGAGGCTGACAATGAGGTAGACGAAGAAGAGGAAGAAGGTGGGGAGGAAGAGGAGGAGG GGAGCAGGAGGCTGACAATGAGGT_________AGAGGAAGAAGGTGGGGAGGAAGAGGAGGAGG TAGACGAAGA T PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:231711751..231712056 26863196 MeRIP-seq:(Medium) rs745795530 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_60392,Human_RBP_ID_205526,Human_RBP_ID_545768,Human_RBP_ID_920682,Human_RBP_ID_1584270,Human_RBP_ID_1912572,Human_RBP_ID_2673878,Human_RBP_ID_3618041,Human_RBP_ID_5196147,Human_RBP_ID_6895184,Human_RBP_ID_8257501,Human_RBP_ID_9103877,Human_RBP_ID_9353842,Human_RBP_ID_9385679,Human_RBP_ID_13794982,Human_RBP_ID_18544623,Human_RBP_ID_22766309,Human_RBP_ID_22997100,Human_RBP_ID_23115084,Human_RBP_ID_23119361,Human_RBP_ID_23856729,Human_RBP_ID_24546253,Human_RBP_ID_26338858,Human_RBP_ID_27818078 Human_Splice_Rec_370018,Human_Splice_Rec_370019,Human_Splice_Rec_370026,Human_Splice_Rec_370027,Human_Splice_Rec_370036,Human_Splice_Rec_370037,Human_Splice_Rec_370044,Human_Splice_Rec_370045,Human_Splice_Rec_370052,Human_Splice_Rec_370053,Human_Splice_Rec_370060,Human_Splice_Rec_370061,Human_Splice_Rec_370065,Human_Splice_Rec_370072,Human_Splice_Rec_370073,Human_Splice_Rec_370078,Human_Splice_Rec_370079,Human_Splice_Rec_370086,Human_Splice_Rec_370087,Human_Splice_Rec_370094 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_119364,RMVar_hsa_circ_207600,RMVar_hsa_circ_371274,RMVar_hsa_circ_207601,RMVar_hsa_circ_207602 97933 RMVar_ID_97933 Human_SNP_ID_116706339 m1A Human chr2 + 231711937 231711937 231711937 GAGCAGGAGGCTGACAATGAGGTAGACGAAGAAGAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGA GAGCAGGAGGCTGACAATGAGGTAGACGAAGAGGAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGA A G PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:231711626..231712045 26863196 MeRIP-seq:(Medium) rs372841592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205526,Human_RBP_ID_545768,Human_RBP_ID_920682,Human_RBP_ID_1584270,Human_RBP_ID_1912572,Human_RBP_ID_2673878,Human_RBP_ID_3618041,Human_RBP_ID_6895184,Human_RBP_ID_8257501,Human_RBP_ID_9103877,Human_RBP_ID_9353842,Human_RBP_ID_9385679,Human_RBP_ID_13794982,Human_RBP_ID_18544623,Human_RBP_ID_22766309,Human_RBP_ID_22997100,Human_RBP_ID_23115084,Human_RBP_ID_23119361,Human_RBP_ID_23856729,Human_RBP_ID_24546253,Human_RBP_ID_26338858,Human_RBP_ID_27818078 Human_Splice_Rec_370018,Human_Splice_Rec_370019,Human_Splice_Rec_370026,Human_Splice_Rec_370027,Human_Splice_Rec_370036,Human_Splice_Rec_370037,Human_Splice_Rec_370044,Human_Splice_Rec_370045,Human_Splice_Rec_370052,Human_Splice_Rec_370053,Human_Splice_Rec_370060,Human_Splice_Rec_370061,Human_Splice_Rec_370065,Human_Splice_Rec_370072,Human_Splice_Rec_370073,Human_Splice_Rec_370078,Human_Splice_Rec_370079,Human_Splice_Rec_370086,Human_Splice_Rec_370087,Human_Splice_Rec_370094 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_119364,RMVar_hsa_circ_207600,RMVar_hsa_circ_371274,RMVar_hsa_circ_207601,RMVar_hsa_circ_207602 97934 RMVar_ID_97934 Human_SNP_ID_116706341 m1A Human chr2 + 231711939 231711939 231711939 GCAGGAGGCTGACAATGAGGTAGACGAAGAAGAGGAAGAAGGTGGGGAGGAAGAGGAGGAGGAAG GCAGGAGGCTGACAATGAGGTAGACGAAGAAGGGGAAGAAGGTGGGGAGGAAGAGGAGGAGGAAG A G PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231711808..231712039 26863196 MeRIP-seq:(Medium) rs1059834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205526,Human_RBP_ID_545768,Human_RBP_ID_920682,Human_RBP_ID_1584270,Human_RBP_ID_1912572,Human_RBP_ID_2673878,Human_RBP_ID_3618041,Human_RBP_ID_6895184,Human_RBP_ID_8257501,Human_RBP_ID_9103877,Human_RBP_ID_9353842,Human_RBP_ID_9385679,Human_RBP_ID_13794982,Human_RBP_ID_18544623,Human_RBP_ID_22766309,Human_RBP_ID_22997100,Human_RBP_ID_23115084,Human_RBP_ID_23119361,Human_RBP_ID_23856729,Human_RBP_ID_24546253,Human_RBP_ID_26338858,Human_RBP_ID_27818078 Human_Splice_Rec_370018,Human_Splice_Rec_370019,Human_Splice_Rec_370026,Human_Splice_Rec_370027,Human_Splice_Rec_370036,Human_Splice_Rec_370037,Human_Splice_Rec_370044,Human_Splice_Rec_370045,Human_Splice_Rec_370052,Human_Splice_Rec_370053,Human_Splice_Rec_370060,Human_Splice_Rec_370061,Human_Splice_Rec_370065,Human_Splice_Rec_370072,Human_Splice_Rec_370073,Human_Splice_Rec_370078,Human_Splice_Rec_370079,Human_Splice_Rec_370086,Human_Splice_Rec_370087,Human_Splice_Rec_370094 RMVar_hsa_circ_207598,RMVar_hsa_circ_96802,RMVar_hsa_circ_375225,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_119364,RMVar_hsa_circ_207600,RMVar_hsa_circ_371274,RMVar_hsa_circ_207601,RMVar_hsa_circ_207602 97935 RMVar_ID_97935 Human_SNP_ID_116706566 m1A Human chr2 - 231712477 231712477 231712477 TCTTCAGCTGCCCGCTTGCCCGTAGCTGACTCAGCTTCCTCATCTTCATCTCCATCCTCTTCCTC TCTTCAGCTGCCCGCTTGCCCGTAGCTGACTCGGCTTCCTCATCTTCATCTCCATCCTCTTCCTC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Starvation treatment;HTR8/Svneo,Normoxia chr2:231711867..231712526;chr2:231712426..231712525 26863410,32194978 MeRIP-seq:(Medium) rs1299294680 Functional Loss SNV dbSNP153 33..33 33 - - - 97936 RMVar_ID_97936 Human_SNP_ID_116706567 m1A Human chr2 - 231712477 231712477 231712477 TCTTCAGCTGCCCGCTTGCCCGTAGCTGACTCAGCTTCCTCATCTTCATCTCCATCCTCTTCCTC TCTTCAGCTGCCCGCTTGCCCGTAGCTGACTCCGCTTCCTCATCTTCATCTCCATCCTCTTCCTC T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Starvation treatment;HTR8/Svneo,Normoxia chr2:231711867..231712526;chr2:231712426..231712525 26863410,32194978 MeRIP-seq:(Medium) rs1299294680 Functional Loss SNV dbSNP153 33..33 33 - - - 97937 RMVar_ID_97937 Human_SNP_ID_116706582 m1A Human chr2 - 231712518 231712518 231712518 GCCAAACCCCCCTTCTTCTCAAGCCAGAACCCACCTCATCATCTTCAGCTGCCCGCTTGCCCGTA GCCAAACCCCCCTTCTTCTCAAGCCAGAACCCTCCTCATCATCTTCAGCTGCCCGCTTGCCCGTA T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr2:231712405..231712569;chr2:231712395..231712569 26863410 MeRIP-seq:(Medium) rs111878292 Functional Loss SNV dbSNP153 33..33 33 - - - 97938 RMVar_ID_97938 Human_SNP_ID_116706583 m1A Human chr2 - 231712518 231712518 231712518 GCCAAACCCCCCTTCTTCTCAAGCCAGAACCCACCTCATCATCTTCAGCTGCCCGCTTGCCCGTA GCCAAACCCCCCTTCTTCTCAAGCCAGAACCCCCCTCATCATCTTCAGCTGCCCGCTTGCCCGTA T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr2:231712405..231712569;chr2:231712395..231712569 26863410 MeRIP-seq:(Medium) rs111878292 Functional Loss SNV dbSNP153 33..33 33 - - - 97939 RMVar_ID_97939 Human_SNP_ID_116706685 m1A Human chr2 - 231712762 231712762 231712762 GAAAGACTGTCAAAGGCCCCTCCAACCCCAGGAGCCCTATCCAGCCCACTGCCTCAGCTCCTGCT GAAAGACTGTCAAAGGCCCCTCCAACCCCAGGGGCCCTATCCAGCCCACTGCCTCAGCTCCTGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:231712757..231713016 26863410 MeRIP-seq:(Medium) rs1448210371 Functional Loss SNV dbSNP153 33..33 33 - - - 97940 RMVar_ID_97940 Human_SNP_ID_116706759 m1A Human chr2 + 231712879 231712876 231712880 ACTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTC ACTAGACAGCAAAAAAGGAAAAGTTAAACT____AAAAAAAGGCCGCCGTGACCTATTCACCCTC TAAAA T PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231712763..231713025 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97941 RMVar_ID_97941 Human_SNP_ID_116706759 m1A Human chr2 + 231712880 231712876 231712880 CTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTCC CTAGACAGCAAAAAAGGAAAAGTTAAACT____AAAAAAAGGCCGCCGTGACCTATTCACCCTCC TAAAA T PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:231712704..231713025;chr2:231712755..231713000;chr2:231712801..231712900 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97942 RMVar_ID_97942 Human_SNP_ID_116706760 m1A Human chr2 + 231712879 231712876 231712880 ACTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTC ACTAGACAGCAAAAAAGGAAAAGTTAAACTA___AAAAAAAGGCCGCCGTGACCTATTCACCCTC TAAAA TA PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231712763..231713025 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97943 RMVar_ID_97943 Human_SNP_ID_116706760 m1A Human chr2 + 231712880 231712876 231712880 CTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTCC CTAGACAGCAAAAAAGGAAAAGTTAAACTA___AAAAAAAGGCCGCCGTGACCTATTCACCCTCC TAAAA TA PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:231712704..231713025;chr2:231712755..231713000;chr2:231712801..231712900 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97944 RMVar_ID_97944 Human_SNP_ID_116706761 m1A Human chr2 + 231712879 231712876 231712880 ACTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTC ACTAGACAGCAAAAAAGGAAAAGTTAAACTAA__AAAAAAAGGCCGCCGTGACCTATTCACCCTC TAAAA TAA PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231712763..231713025 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97945 RMVar_ID_97945 Human_SNP_ID_116706761 m1A Human chr2 + 231712880 231712876 231712880 CTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTCC CTAGACAGCAAAAAAGGAAAAGTTAAACTAA__AAAAAAAGGCCGCCGTGACCTATTCACCCTCC TAAAA TAA PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:231712704..231713025;chr2:231712755..231713000;chr2:231712801..231712900 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97946 RMVar_ID_97946 Human_SNP_ID_116706762 m1A Human chr2 + 231712880 231712876 231712880 CTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTCC CTAGACAGCAAAAAAGGAAAAGTTAAACTAAA_AAAAAAAGGCCGCCGTGACCTATTCACCCTCC TAAAA TAAA PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:231712704..231713025;chr2:231712755..231713000;chr2:231712801..231712900 26863196 MeRIP-seq:(Medium) rs368863947 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97947 RMVar_ID_97947 Human_SNP_ID_116706770 m1A Human chr2 + 231712886 231712886 231712886 AGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTCCACTTCC AGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAGAGGCCGCCGTGACCTATTCACCCTCCACTTCC A G PTMA Ensembl:ENSG00000187514 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782896,GSM1782897 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA Untreated, competitive elution chr2:231712801..231712925 31548705,26863196 m1A-IP-seq:(High) rs563464274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627111,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 Human_miRNA_ID_2513967 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 97948 RMVar_ID_97948 Human_SNP_ID_116723184 m1A Human chr2 + 231781232 231781232 231781232 GCCCGGCTTGGAGACCTCGGGCTAGCAGCCGCAGCGGCCAGACCAGGACCGGCCTCTCTCTCCCC GCCCGGCTTGGAGACCTCGGGCTAGCAGCCGCTGCGGCCAGACCAGGACCGGCCTCTCTCTCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:231780874..231781300;chr2:231781051..231781275;chr2:231780883..231781275 26863196 MeRIP-seq:(Medium) rs993391794 Functional Loss SNV dbSNP153 33..33 33 - - - 97949 RMVar_ID_97949 Human_SNP_ID_116723187 m1A Human chr2 + 231781239 231781239 231781239 TTGGAGACCTCGGGCTAGCAGCCGCAGCGGCCAGACCAGGACCGGCCTCTCTCTCCCCTCAGCTC TTGGAGACCTCGGGCTAGCAGCCGCAGCGGCCGGACCAGGACCGGCCTCTCTCTCCCCTCAGCTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231781115..231781252 26863196 MeRIP-seq:(Medium) rs550036653 Functional Loss SNV dbSNP153 33..33 33 - - - 97950 RMVar_ID_97950 Human_SNP_ID_116723188 m1A Human chr2 + 231781239 231781239 231781239 TTGGAGACCTCGGGCTAGCAGCCGCAGCGGCCAGACCAGGACCGGCCTCTCTCTCCCCTCAGCTC TTGGAGACCTCGGGCTAGCAGCCGCAGCGGCCTGACCAGGACCGGCCTCTCTCTCCCCTCAGCTC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231781115..231781252 26863196 MeRIP-seq:(Medium) rs550036653 Functional Loss SNV dbSNP153 33..33 33 - - - 97951 RMVar_ID_97951 Human_SNP_ID_116728473 m1A Human chr2 + 231803165 231803165 231803165 TGGGAGGCCATCGAAGAGGGAGAGGCACTGCCAGGCAAGTACAGATTGAAGGGTGGCAGATCAGT TGGGAGGCCATCGAAGAGGGAGAGGCACTGCCGGGCAAGTACAGATTGAAGGGTGGCAGATCAGT A G COPS7B Ensembl:ENSG00000144524 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:231803163..231803396 26863196 MeRIP-seq:(Medium) rs975974038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115299,RMVar_hsa_circ_207609 97952 RMVar_ID_97952 Human_SNP_ID_116784106 m1A Human chr2 - 231922289 231922289 231922289 TTTCAGGATCGGGAACTGGCTCCGTTGTGCTGAGGTCATCTTTGGTCATCAGCCTCCAGCATCTG TTTCAGGATCGGGAACTGGCTCCGTTGTGCTGGGGTCATCTTTGGTCATCAGCCTCCAGCATCTG T C NPPC Ensembl:ENSG00000163273 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:231922208..231922306 26863410 MeRIP-seq:(Medium) rs895469452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280719,Human_RBP_ID_18443203 Human_Splice_Rec_370322 97953 RMVar_ID_97953 Human_SNP_ID_116784939 m1A Human chr2 - 231925511 231925511 231925511 TTCTGCAAGAGCACCCCAACGCGCGCAAATACAAAGGAGCCAACAAGAAGGGCTTGTCCAAGGGC TTCTGCAAGAGCACCCCAACGCGCGCAAATACGAAGGAGCCAACAAGAAGGGCTTGTCCAAGGGC T C NPPC Ensembl:ENSG00000163273 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231925461..231925590 26863196 MeRIP-seq:(Medium) rs962257798 Functional Loss SNV dbSNP153 33..33 33 - - - 97954 RMVar_ID_97954 Human_SNP_ID_116828842 m1A Human chr2 + 232112778 232112778 232112778 CAAGAGGAACAGATTTGCAGGCAGAAGGAGGGACCATTCAGAGAGGAAGGGGGACAAGGTAAAAG CAAGAGGAACAGATTTGCAGGCAGAAGGAGGGCCCATTCAGAGAGGAAGGGGGACAAGGTAAAAG A C DIS3L2 Ensembl:ENSG00000144535 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232112759..232112968 26863196 MeRIP-seq:(Medium) rs1313128939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33231,RMVar_hsa_circ_52435,RMVar_hsa_circ_348928,RMVar_hsa_circ_370507,RMVar_hsa_circ_324981,RMVar_hsa_circ_60584,RMVar_hsa_circ_207611,RMVar_hsa_circ_85107,RMVar_hsa_circ_40346,RMVar_hsa_circ_303049,RMVar_hsa_circ_371641,RMVar_hsa_circ_375550,RMVar_hsa_circ_352802,RMVar_hsa_circ_94687,RMVar_hsa_circ_85901,RMVar_hsa_circ_207620,RMVar_hsa_circ_207621,RMVar_hsa_circ_207622,RMVar_hsa_circ_207619,RMVar_hsa_circ_207623 97955 RMVar_ID_97955 Human_SNP_ID_116855308 m1A Human chr2 - 232232871 232232871 232232871 GTGTGGCGTGCCAAGCCTCCGTGCTCTGCCCCAGGCTGCCTTCTCTTCTAATTCTACCCCTTCTC GTGTGGCGTGCCAAGCCTCCGTGCTCTGCCCCCGGCTGCCTTCTCTTCTAATTCTACCCCTTCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232232869..232232945 26863196 MeRIP-seq:(Medium) rs1337238822 Functional Loss SNV dbSNP153 33..33 33 - - - 97956 RMVar_ID_97956 Human_SNP_ID_116858578 m1A Human chr2 - 232247648 232247634 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGC______________CCCCCCCCCCCCCCCCCCG GGCGGGGGGGAGGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1559173634 Functional Loss DEL dbSNP153 33..46 33 - - - 97957 RMVar_ID_97957 Human_SNP_ID_116858582 m1A Human chr2 - 232247648 232247635 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGC_____________CCCCCCCCCCCCCCCCCCCG GCGGGGGGGAGGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1559173645 Functional Loss DEL dbSNP153 33..45 33 - - - 97958 RMVar_ID_97958 Human_SNP_ID_116858598 m1A Human chr2 - 232247648 232247642 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGC______CCCCCCGCCCCCCCCCCCCCCCCCCCG GGAGGGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1559173670 Functional Loss DEL dbSNP153 33..38 33 - - - 97959 RMVar_ID_97959 Human_SNP_ID_116858601 m1A Human chr2 - 232247648 232247644 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGC____TCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGGGT A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1559173675 Functional Loss DEL dbSNP153 33..36 33 - - - 97960 RMVar_ID_97960 Human_SNP_ID_116858607 m1A Human chr2 - 232247648 232247646 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGC__CCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG GGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1253451659 Functional Loss DEL dbSNP153 33..34 33 - - - 97961 RMVar_ID_97961 Human_SNP_ID_116858609 m1A Human chr2 - 232247648 232247648 232247648 AGCCTTTGGGCTATCCTAGGGACTGAATTGGCACCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG AGCCTTTGGGCTATCCTAGGGACTGAATTGGCCCCCTCCCCCCCGCCCCCCCCCCCCCCCCCCCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:232247601..232247675 26863196 MeRIP-seq:(Medium) rs1479171635 Functional Loss SNV dbSNP153 33..33 33 - - - 97962 RMVar_ID_97962 Human_SNP_ID_116879992 m1A Human chr2 + 232336560 232336560 232336560 GTACAGCGCCATCCTGAAGCGGCCAGGCACCCAGGGCCACCTGGGCCCTGAGAAGGAGGAGGAGG GTACAGCGCCATCCTGAAGCGGCCAGGCACCCGGGGCCACCTGGGCCCTGAGAAGGAGGAGGAGG A G DIS3L2 Ensembl:ENSG00000144535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232336527..232336629 26863196 MeRIP-seq:(Medium) rs777191235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370388,Human_Splice_Rec_370440,Human_Splice_Rec_370524 Clinvar_Rec_596 RMVar_hsa_circ_112846,RMVar_hsa_circ_207630,RMVar_hsa_circ_95796,RMVar_hsa_circ_207635,RMVar_hsa_circ_101550,RMVar_hsa_circ_207639 97963 RMVar_ID_97963 Human_SNP_ID_116879993 m1A Human chr2 + 232336560 232336560 232336560 GTACAGCGCCATCCTGAAGCGGCCAGGCACCCAGGGCCACCTGGGCCCTGAGAAGGAGGAGGAGG GTACAGCGCCATCCTGAAGCGGCCAGGCACCCTGGGCCACCTGGGCCCTGAGAAGGAGGAGGAGG A T DIS3L2 Ensembl:ENSG00000144535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232336527..232336629 26863196 MeRIP-seq:(Medium) rs777191235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370388,Human_Splice_Rec_370440,Human_Splice_Rec_370524 Clinvar_Rec_596 RMVar_hsa_circ_112846,RMVar_hsa_circ_207630,RMVar_hsa_circ_95796,RMVar_hsa_circ_207635,RMVar_hsa_circ_101550,RMVar_hsa_circ_207639 97964 RMVar_ID_97964 Human_SNP_ID_116891730 m1A Human chr2 - 232378785 232378785 232378785 GCAGGGCCCCAGCATGTCTGGAGGGCAGCAGGACAGTGGCGAGGCAGGAATTCTGGGCATGGAGT GCAGGGCCCCAGCATGTCTGGAGGGCAGCAGGTCAGTGGCGAGGCAGGAATTCTGGGCATGGAGT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:232378676..232378900;chr2:232378676..232378876 26863196 MeRIP-seq:(Medium) rs767270931 Functional Loss SNV dbSNP153 33..33 33 - - - 97965 RMVar_ID_97965 Human_SNP_ID_116891731 m1A Human chr2 - 232378785 232378785 232378785 GCAGGGCCCCAGCATGTCTGGAGGGCAGCAGGACAGTGGCGAGGCAGGAATTCTGGGCATGGAGT GCAGGGCCCCAGCATGTCTGGAGGGCAGCAGGCCAGTGGCGAGGCAGGAATTCTGGGCATGGAGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:232378676..232378900;chr2:232378676..232378876 26863196 MeRIP-seq:(Medium) rs767270931 Functional Loss SNV dbSNP153 33..33 33 - - - 97966 RMVar_ID_97966 Human_SNP_ID_116893279 m1A Human chr2 - 232381889 232381889 232381889 CATGGCAGGACCTCTGTATAGGGACTCCGGGGATGACGACTCGGGCTGGAGGCCAGGCAGGACGA CATGGCAGGACCTCTGTATAGGGACTCCGGGGCTGACGACTCGGGCTGGAGGCCAGGCAGGACGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:232381670..232382162;chr2:232381666..232382118 26863196 MeRIP-seq:(Medium) rs796856652 Functional Loss SNV dbSNP153 33..33 33 - - - 97967 RMVar_ID_97967 Human_SNP_ID_116893457 m1A Human chr2 - 232382354 232382354 232382354 TTGAGATTTGGGGCAAGCCTTTGCCATGAGGCAGAGGGCCCCCTGGGGGGGTACAGGGGTGTGGA TTGAGATTTGGGGCAAGCCTTTGCCATGAGGCTGAGGGCCCCCTGGGGGGGTACAGGGGTGTGGA T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:232382351..232382425 26863196 MeRIP-seq:(Medium) rs971840897 Functional Loss SNV dbSNP153 33..33 33 - - - 97968 RMVar_ID_97968 Human_SNP_ID_116893522 m1A Human chr2 + 232382532 232382530 232382533 CAGACATCTGGACACTGGGCATAGATTTCTCAAGAAGGAAGACTCCCCTGCCTCCCCAGGGCCTC CAGACATCTGGACACTGGGCATAGATTTCTC___AAGGAAGACTCCCCTGCCTCCCCAGGGCCTC CAAG C ALPP Ensembl:ENSG00000163283 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232382481..232382606 26863196 MeRIP-seq:(Medium) rs1321062808 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_61600,Human_RBP_ID_26480562 Human_miRNA_ID_1690067 97969 RMVar_ID_97969 Human_SNP_ID_116894316 m1A Human chr2 + 232385175 232385165 232385176 AGGAGGAGGAGGAGGAGGAGGAGGAAAAGAAGAAGAGGAGGAGGAAGAGGAAGAGGAGGAGGAAG AGGAGGAGGAGGAGGAGGAGGAG___________GAGGAGGAGGAAGAGGAAGAGGAGGAGGAAG GGAAAAGAAGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232385172..232385350 26863196 MeRIP-seq:(Medium) rs1267580892 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_2627304 97970 RMVar_ID_97970 Human_SNP_ID_116914195 m1A Human chr2 + 232457069 232457069 232457069 GAGGTCATCTCCGTGATGAACCGGGCCAAGCAAGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGG GAGGTCATCTCCGTGATGAACCGGGCCAAGCAGGCAGGTGAGCTGGGGCCCGCTGTGGGGTCAGG A G ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232456874..232457899 26863196 MeRIP-seq:(Medium) rs1026987984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370713,Human_Splice_Rec_370733 97971 RMVar_ID_97971 Human_SNP_ID_116914230 m1A Human chr2 - 232457155 232457155 232457155 CTGCACCCGTGTGGTGGTCACCACTCCTACTGACTTTCCTGAGGGTGACAGAGGTCAGGATCGGT CTGCACCCGTGTGGTGGTCACCACTCCTACTGGCTTTCCTGAGGGTGACAGAGGTCAGGATCGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232456905..232457482 26863196 MeRIP-seq:(Medium) rs1232159721 Functional Loss SNV dbSNP153 33..33 33 - - - 97972 RMVar_ID_97972 Human_SNP_ID_116914457 m1A Human chr2 + 232457680 232457680 232457680 AATCAGGCTGGACGGGAAGAACCTGGTGCAGGAATGGCTGGCAAAGCACCAGGTGATGGGGGCTG AATCAGGCTGGACGGGAAGAACCTGGTGCAGGGATGGCTGGCAAAGCACCAGGTGATGGGGGCTG A G ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232457535..232457700 26863196 MeRIP-seq:(Medium) rs751483451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370717,Human_Splice_Rec_370737 97973 RMVar_ID_97973 Human_SNP_ID_116914623 m1A Human chr2 + 232458040 232458040 232458040 GCCCGGAGACACGAAATATGAGATCCACCGAGACCCCACACTGGACCCCTCCCTGATGGAGATGA GCCCGGAGACACGAAATATGAGATCCACCGAGGCCCCACACTGGACCCCTCCCTGATGGAGATGA A G ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232457946..232458049 26863196 MeRIP-seq:(Medium) rs377672298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27158458 Human_Splice_Rec_370720,Human_Splice_Rec_370721,Human_Splice_Rec_370740,Human_Splice_Rec_370741 97974 RMVar_ID_97974 Human_SNP_ID_116914624 m1A Human chr2 + 232458040 232458040 232458040 GCCCGGAGACACGAAATATGAGATCCACCGAGACCCCACACTGGACCCCTCCCTGATGGAGATGA GCCCGGAGACACGAAATATGAGATCCACCGAGTCCCCACACTGGACCCCTCCCTGATGGAGATGA A T ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232457946..232458049 26863196 MeRIP-seq:(Medium) rs377672298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27158458 Human_Splice_Rec_370720,Human_Splice_Rec_370721,Human_Splice_Rec_370740,Human_Splice_Rec_370741 97975 RMVar_ID_97975 Human_SNP_ID_116914966 m1A Human chr2 - 232458754 232458754 232458754 CCCTGGTCCCCCTGCACGGGCCATTCAGCCTCACTCACCGCTCTCGCTCTCATTCACGTCTGGTC CCCTGGTCCCCCTGCACGGGCCATTCAGCCTCCCTCACCGCTCTCGCTCTCATTCACGTCTGGTC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr2:232458751..232458775;chr2:232458751..232458800 26863196 MeRIP-seq:(Medium) rs1315770969 Functional Loss SNV dbSNP153 33..33 33 - - - 97976 RMVar_ID_97976 Human_SNP_ID_116915211 m1A Human chr2 - 232459205 232459205 232459205 CTGTGTGTGTTCGCTGGAAGTGGCGGCTCAGGACGGGGAACAGGGCAGGACGCCCGGAGGTGGGG CTGTGTGTGTTCGCTGGAAGTGGCGGCTCAGGGCGGGGAACAGGGCAGGACGCCCGGAGGTGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232457956..232460584 26863196 MeRIP-seq:(Medium) rs1212002097 Functional Loss SNV dbSNP153 33..33 33 - - - 97977 RMVar_ID_97977 Human_SNP_ID_116915387 m1A Human chr2 - 232459881 232459881 232459881 GCCCATGGGCTCTGGGTTGCTGCCCTGTACCCAGAGCTCCTCAAGCGCTCCTTGGATCTGGTGAC GCCCATGGGCTCTGGGTTGCTGCCCTGTACCCGGAGCTCCTCAAGCGCTCCTTGGATCTGGTGAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:232459831..232460484 26863196 MeRIP-seq:(Medium) rs1249324192 Functional Loss SNV dbSNP153 33..33 33 - - - 97978 RMVar_ID_97978 Human_SNP_ID_116915490 m1A Human chr2 + 232460304 232460304 232460304 AAAGCCTGAGGGGTCAGGAGAGTGGGGTGTGCATGGGGGACTGTGAAGTCTGGTTAGAGGGGTGT AAAGCCTGAGGGGTCAGGAGAGTGGGGTGTGCCTGGGGGACTGTGAAGTCTGGTTAGAGGGGTGT A C ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:232460301..232460325 26863196 MeRIP-seq:(Medium) rs1032125249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27478367 97979 RMVar_ID_97979 Human_SNP_ID_116928226 m1A Human chr2 - 232507336 232507336 232507336 CTTGTTTTCAGTATCATCTTGTTTACACAGACATGGCTGGGCCTAGAGAAATAATAAGATGAATG CTTGTTTTCAGTATCATCTTGTTTACACAGACGTGGCTGGGCCTAGAGAAATAATAAGATGAATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232507329..232507422 26863196 MeRIP-seq:(Medium) rs1015170229 Functional Loss SNV dbSNP153 33..33 33 - - - 97980 RMVar_ID_97980 Human_SNP_ID_116931565 m1A Human chr2 + 232520529 232520529 232520529 GCCGAAAGGCAGCAGAAGGCGGGCACCAAAGGATAGGCACCCGGAAGGTGGACTCCGAGGAGGAG GCCGAAAGGCAGCAGAAGGCGGGCACCAAAGGGTAGGCACCCGGAAGGTGGACTCCGAGGAGGAG A G PRSS56 Ensembl:ENSG00000237412 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:232520401..232520743 26863196 MeRIP-seq:(Medium) rs974354192 Functional Loss SNV dbSNP153 33..33 33 - - - 97981 RMVar_ID_97981 Human_SNP_ID_116931934 m1A Human chr2 - 232521555 232521555 232521555 CTCGGAGAGACAGACCTTCACAAACGTAGTCTAGGTTGCGGCCCAACACAGTCTCTGCCCCCAAG CTCGGAGAGACAGACCTTCACAAACGTAGTCTGGGTTGCGGCCCAACACAGTCTCTGCCCCCAAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:232521551..232521575 26863196 MeRIP-seq:(Medium) rs74372338 Functional Loss SNV dbSNP153 33..33 33 - - - 97982 RMVar_ID_97982 Human_SNP_ID_116932259 m1A Human chr2 + 232522430 232522430 232522430 CCCTCCGTGCCCCCAGGTGGAGAAAGCCCGGCATGCGGGCGGAGGGGCAGGGTCTCCGAGGGGCC CCCTCCGTGCCCCCAGGTGGAGAAAGCCCGGCGTGCGGGCGGAGGGGCAGGGTCTCCGAGGGGCC A G PRSS56 Ensembl:ENSG00000237412 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:232522426..232522500 26863196 MeRIP-seq:(Medium) rs543118690 Functional Loss SNV dbSNP153 33..33 33 - - - 97983 RMVar_ID_97983 Human_SNP_ID_116932696 m1A Human chr2 + 232523544 232523544 232523544 CCAGGGAAGCCCGGGGTCTACACCCGCGTGGCAGTGTTCAAGGACTGGCTCCAGGAGCAGATGAG CCAGGGAAGCCCGGGGTCTACACCCGCGTGGCCGTGTTCAAGGACTGGCTCCAGGAGCAGATGAG A C PRSS56 Ensembl:ENSG00000237412 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232523408..232523607 26863196 MeRIP-seq:(Medium) rs1167103390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370869 97984 RMVar_ID_97984 Human_SNP_ID_116932701 m1A Human chr2 + 232523555 232523555 232523555 CGGGGTCTACACCCGCGTGGCAGTGTTCAAGGACTGGCTCCAGGAGCAGATGAGCGGTGAGCGCC CGGGGTCTACACCCGCGTGGCAGTGTTCAAGGCCTGGCTCCAGGAGCAGATGAGCGGTGAGCGCC A C PRSS56 Ensembl:ENSG00000237412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:232523374..232524229;chr2:232523374..232524294;chr2:232523381..232523638;chr2:232523401..232523629 26863196 MeRIP-seq:(Medium) rs12617886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370869 97985 RMVar_ID_97985 Human_SNP_ID_116932754 m1A Human chr2 + 232523733 232523733 232523733 TTCCGGGGAAGGAGTGAGGGGGCTAGGGCCCCAAACAGAGGGTGAGCTGACCCCTGTCCCGCCCG TTCCGGGGAAGGAGTGAGGGGGCTAGGGCCCCCAACAGAGGGTGAGCTGACCCCTGTCCCGCCCG A C PRSS56 Ensembl:ENSG00000237412 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:232523729..232523894 26863196 MeRIP-seq:(Medium) rs776790868 Functional Loss SNV dbSNP153 33..33 33 - - - 97986 RMVar_ID_97986 Human_SNP_ID_116932837 m1A Human chr2 + 232523941 232523941 232523941 GCGCACCAGCAGTGCCTGCAGCGCCGGCGGCGATGCGGTCAGTTCTGTTCACCCGGACCCGGACG GCGCACCAGCAGTGCCTGCAGCGCCGGCGGCGTTGCGGTCAGTTCTGTTCACCCGGACCCGGACG A T PRSS56 Ensembl:ENSG00000237412 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232523701..232524404 26863196 MeRIP-seq:(Medium) rs898076879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_370871 97987 RMVar_ID_97987 Human_SNP_ID_116932838 m1A Human chr2 - 232523942 232523942 232523942 CCGTCCGGGTCCGGGTGAACAGAACTGACCGCATCGCCGCCGGCGCTGCAGGCACTGCTGGTGCG CCGTCCGGGTCCGGGTGAACAGAACTGACCGCGTCGCCGCCGGCGCTGCAGGCACTGCTGGTGCG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:232523892..232524074 26863196 MeRIP-seq:(Medium) rs730882161 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_597 97988 RMVar_ID_97988 Human_SNP_ID_116933412 m1A Human chr2 + 232525342 232525342 232525342 TGGTGGGCCTGGAGCCGGCCACACTGGCTCGCAGCCTCCCCCGGCTGCTGGTGCAGGCCCTGCAG TGGTGGGCCTGGAGCCGGCCACACTGGCTCGCGGCCTCCCCCGGCTGCTGGTGCAGGCCCTGCAG A G PRSS56 Ensembl:ENSG00000237412 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:232525292..232525621 26863196 MeRIP-seq:(Medium) rs1220533396 Functional Loss SNV dbSNP153 33..33 33 - - - 97989 RMVar_ID_97989 Human_SNP_ID_116933447 m1A Human chr2 + 232525423 232525423 232525423 CCCTGGCAGAAGGGGAGCCCGAGGGACCCTGGATGGATGTAGGGCAGGGGCCCGGGCTGGAGAGG CCCTGGCAGAAGGGGAGCCCGAGGGACCCTGGGTGGATGTAGGGCAGGGGCCCGGGCTGGAGAGG A G PRSS56 Ensembl:ENSG00000237412 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:232525309..232525581 26863196 MeRIP-seq:(Medium) rs1239936195 Functional Loss SNV dbSNP153 33..33 33 - - - 97990 RMVar_ID_97990 Human_SNP_ID_116941695 m1A Human chr2 - 232550737 232550737 232550737 CCGGGGGCGGCCACGAGCCACTCACGCGTCGAACTTGTTGTTCATCCTCTCGCCGCCGCTGTCGC CCGGGGGCGGCCACGAGCCACTCACGCGTCGAGCTTGTTGTTCATCCTCTCGCCGCCGCTGTCGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232550651..232550860 26863196 MeRIP-seq:(Medium) rs1559309972 Functional Loss SNV dbSNP153 33..33 33 - - - 97991 RMVar_ID_97991 Human_SNP_ID_116943111 m1A Human chr2 - 232556373 232556373 232556373 AGGCAACACAATACAATTCTGTGACGAAGTCAATTCTTGCTTACCTAACAAAGCCACCAGGTCAT AGGCAACACAATACAATTCTGTGACGAAGTCAGTTCTTGCTTACCTAACAAAGCCACCAGGTCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:232556371..232556583;chr2:232556371..232556573 26863196 MeRIP-seq:(Medium) rs768378345 Functional Loss SNV dbSNP153 33..33 33 - - - 97992 RMVar_ID_97992 Human_SNP_ID_116943112 m1A Human chr2 - 232556373 232556373 232556373 AGGCAACACAATACAATTCTGTGACGAAGTCAATTCTTGCTTACCTAACAAAGCCACCAGGTCAT AGGCAACACAATACAATTCTGTGACGAAGTCACTTCTTGCTTACCTAACAAAGCCACCAGGTCAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:232556371..232556583;chr2:232556371..232556573 26863196 MeRIP-seq:(Medium) rs768378345 Functional Loss SNV dbSNP153 33..33 33 - - - 97993 RMVar_ID_97993 Human_SNP_ID_116943116 m1A Human chr2 + 232556384 232556384 232556384 GCTTTGTTAGGTAAGCAAGAATTGACTTCGTCACAGAATTGTATTGTGTTGCCTTTCCATTCAGT GCTTTGTTAGGTAAGCAAGAATTGACTTCGTCGCAGAATTGTATTGTGTTGCCTTTCCATTCAGT A G EIF4E2 Ensembl:ENSG00000135930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232556381..232556573 26863196 MeRIP-seq:(Medium) rs1372278397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85411,RMVar_hsa_circ_207640 97994 RMVar_ID_97994 Human_SNP_ID_116943117 m1A Human chr2 + 232556384 232556384 232556384 GCTTTGTTAGGTAAGCAAGAATTGACTTCGTCACAGAATTGTATTGTGTTGCCTTTCCATTCAGT GCTTTGTTAGGTAAGCAAGAATTGACTTCGTCTCAGAATTGTATTGTGTTGCCTTTCCATTCAGT A T EIF4E2 Ensembl:ENSG00000135930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232556381..232556573 26863196 MeRIP-seq:(Medium) rs1372278397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85411,RMVar_hsa_circ_207640 97995 RMVar_ID_97995 Human_SNP_ID_116943463 m1A Human chr2 - 232557822 232557822 232557822 GGGCATTTGTCACGTGGTCTGAGACTGAGAGAACATTTTGCAGTGTCAATCCTTACCACCTCCAC GGGCATTTGTCACGTGGTCTGAGACTGAGAGACCATTTTGCAGTGTCAATCCTTACCACCTCCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232557818..232557975 26863196 MeRIP-seq:(Medium) rs1172553908 Functional Loss SNV dbSNP153 33..33 33 - - - 97996 RMVar_ID_97996 Human_SNP_ID_116943472 m1A Human chr2 + 232557840 232557840 232557840 GACACTGCAAAATGTTCTCTCAGTCTCAGACCACGTGACAAATGCCCAGGACTAACACACCTTCT GACACTGCAAAATGTTCTCTCAGTCTCAGACCGCGTGACAAATGCCCAGGACTAACACACCTTCT A G EIF4E2 Ensembl:ENSG00000135930 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232557837..232558025 26863196 MeRIP-seq:(Medium) rs1365346021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85411,RMVar_hsa_circ_207641,RMVar_hsa_circ_311276,RMVar_hsa_circ_207640,RMVar_hsa_circ_310048 97997 RMVar_ID_97997 Human_SNP_ID_116946361 m1A Human chr2 - 232568901 232568899 232568901 GCAAAAGGTTGGCTCATTGGGAGAGGAAAGAGAGGGGGACGCAAGGGAAAGTAGCATCTGGGTCT GCAAAAGGTTGGCTCATTGGGAGAGGAAAGAG__GGGGACGCAAGGGAAAGTAGCATCTGGGTCT CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232568895..232568966 26863196 MeRIP-seq:(Medium) rs779215671 Functional Loss DEL dbSNP153 33..34 33 - - - 97998 RMVar_ID_97998 Human_SNP_ID_116949386 m1A Human chr2 + 232581296 232581296 232581296 TGTTGTACGAAGGGTACCGTGGCCACGTGTACATGCCAGAGCTGTTGATGAGAGTTACCAGTATT TGTTGTACGAAGGGTACCGTGGCCACGTGTACGTGCCAGAGCTGTTGATGAGAGTTACCAGTATT A G EIF4E2 Ensembl:ENSG00000135930 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:232581195..232581345 26863410 MeRIP-seq:(Medium) rs1233740655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_545929,Human_RBP_ID_17965784,Human_RBP_ID_23857141 Human_miRNA_ID_1224895,Human_miRNA_ID_2586228,Human_miRNA_ID_2586229 RMVar_hsa_circ_93561,RMVar_hsa_circ_207645,RMVar_hsa_circ_112704,RMVar_hsa_circ_207651 97999 RMVar_ID_97999 Human_SNP_ID_116949390 m1A Human chr2 + 232581326 232581326 232581326 ACATGCCAGAGCTGTTGATGAGAGTTACCAGTATTATGAATGTCTGTGCATCCAGGAAAAGTGTT ACATGCCAGAGCTGTTGATGAGAGTTACCAGTCTTATGAATGTCTGTGCATCCAGGAAAAGTGTT A C EIF4E2 Ensembl:ENSG00000135930 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232581284..232581369 26863196 MeRIP-seq:(Medium) rs1367931885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1912686,Human_RBP_ID_17965784,Human_RBP_ID_23857141 Human_miRNA_ID_393645,Human_miRNA_ID_399720,Human_miRNA_ID_405716,Human_miRNA_ID_411686,Human_miRNA_ID_532387,Human_miRNA_ID_538592,Human_miRNA_ID_1087222,Human_miRNA_ID_1255115,Human_miRNA_ID_2118626,Human_miRNA_ID_2118627,Human_miRNA_ID_2121844,Human_miRNA_ID_2121845,Human_miRNA_ID_2125061,Human_miRNA_ID_2125062,Human_miRNA_ID_2128282,Human_miRNA_ID_2128283,Human_miRNA_ID_2186916,Human_miRNA_ID_2186917,Human_miRNA_ID_2189280,Human_miRNA_ID_2189281,Human_miRNA_ID_2507312,Human_miRNA_ID_2507313,Human_miRNA_ID_2600913,Human_miRNA_ID_2600914,Human_miRNA_ID_2604047,Human_miRNA_ID_2604048 RMVar_hsa_circ_93561,RMVar_hsa_circ_207645,RMVar_hsa_circ_112704,RMVar_hsa_circ_207651 98000 RMVar_ID_98000 Human_SNP_ID_116963201 m1A Human chr2 + 232633634 232633633 232633634 GCGGAGTGTTGTAGAGCCTCGAGCCTGCGAGGAGCGCGCCGCCCGCCAGCTCCCTGCGTCCCGTC GCGGAGTGTTGTAGAGCCTCGAGCCTGCGAGG_GCGCGCCGCCCGCCAGCTCCCTGCGTCCCGTC GA G EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232633600..232633795 26863196 MeRIP-seq:(Medium) rs1236125294 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 98001 RMVar_ID_98001 Human_SNP_ID_116963202 m1A Human chr2 + 232633634 232633634 232633634 GCGGAGTGTTGTAGAGCCTCGAGCCTGCGAGGAGCGCGCCGCCCGCCAGCTCCCTGCGTCCCGTC GCGGAGTGTTGTAGAGCCTCGAGCCTGCGAGGGGCGCGCCGCCCGCCAGCTCCCTGCGTCCCGTC A G EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:232633600..232633795 26863196 MeRIP-seq:(Medium) rs1209833621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 98002 RMVar_ID_98002 Human_SNP_ID_116963220 m1A Human chr2 - 232633681 232633673 232633681 ACTGGCCATGGCGGCGGATCGCAGGACGCGGGAACGCGGGGACGCGGGACGGGACGCAGGGAGCT ACTGGCCATGGCGGCGGATCGCAGGACGCGGG________GACGCGGGACGGGACGCAGGGAGCT CCCCGCGTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:232633553..232633898 26863410 MeRIP-seq:(Medium) rs922636432 Functional Loss DEL dbSNP153 33..40 33 - - - 98003 RMVar_ID_98003 Human_SNP_ID_116963228 m1A Human chr2 - 232633681 232633681 232633681 ACTGGCCATGGCGGCGGATCGCAGGACGCGGGAACGCGGGGACGCGGGACGGGACGCAGGGAGCT ACTGGCCATGGCGGCGGATCGCAGGACGCGGGGACGCGGGGACGCGGGACGGGACGCAGGGAGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:232633553..232633898 26863410 MeRIP-seq:(Medium) rs1401836440 Functional Loss SNV dbSNP153 33..33 33 - - - 98004 RMVar_ID_98004 Human_SNP_ID_116963342 m1A Human chr2 + 232633897 232633897 232633897 AGCTGAGCGCCCAGCTGAGCCGGCGGCTGGACATCAACGAGGGCGCTGCGCGGCCCCGGCGCTGC AGCTGAGCGCCCAGCTGAGCCGGCGGCTGGACGTCAACGAGGGCGCTGCGCGGCCCCGGCGCTGC A G EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232633861..232633935 26863196 MeRIP-seq:(Medium) rs1157930340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 98005 RMVar_ID_98005 Human_SNP_ID_116977819 m1A Human chr2 - 232688496 232688486 232688497 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAA___________GAAAAGAAAAAGAAAAAATACTA CTTTTTTTTTTT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs71398736 Functional Loss DEL dbSNP153 32..42 33 - - - 98006 RMVar_ID_98006 Human_SNP_ID_116977820 m1A Human chr2 - 232688496 232688486 232688497 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAA__________AGAAAAGAAAAAGAAAAAATACTA CTTTTTTTTTTT CT - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs71398736 Functional Loss DEL dbSNP153 32..41 33 - - - 98007 RMVar_ID_98007 Human_SNP_ID_116977821 m1A Human chr2 - 232688496 232688486 232688497 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAA_________AAGAAAAGAAAAAGAAAAAATACTA CTTTTTTTTTTT CTT - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs71398736 Functional Loss DEL dbSNP153 32..40 33 - - - 98008 RMVar_ID_98008 Human_SNP_ID_116977822 m1A Human chr2 - 232688496 232688486 232688497 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAA_______AAAAGAAAAGAAAAAGAAAAAATACTA CTTTTTTTTTTT CTTTT - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs71398736 Functional Loss DEL dbSNP153 32..38 33 - - - 98009 RMVar_ID_98009 Human_SNP_ID_116977823 m1A Human chr2 - 232688496 232688486 232688497 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAA__AAAAAAAAAGAAAAGAAAAAGAAAAAATACTA CTTTTTTTTTTT CTTTTTTTTT - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs71398736 Functional Loss DEL dbSNP153 32..33 33 - - - 98010 RMVar_ID_98010 Human_SNP_ID_116977839 m1A Human chr2 - 232688496 232688496 232688496 GCGACAGAGCAACACCCTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA GCGACAGAGCAACACCCTGTCTCAAAAAAAAAGAAAAAAAAAGAAAAGAAAAAGAAAAAATACTA T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:232688475..232688557 26863410 MeRIP-seq:(Medium) rs1040465823 Functional Loss SNV dbSNP153 33..33 33 - - - 98011 RMVar_ID_98011 Human_SNP_ID_116980044 m1A Human chr2 - 232697433 232697411 232697434 GCCCGGGACGCGGCGGCGGGGCCGGGGCGCGGAGCAGAGCCGGGCAGGGGAGCGACACGGAACGG GCCCGGGACGCGGCGGCGGGGCCGGGGCGCG_______________________ACACGGAACGG TCGCTCCCCTGCCCGGCTCTGCTC T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:232697383..232697499 26863196 MeRIP-seq:(Medium) rs1224838109 Functional Loss DEL dbSNP153 32..54 33 - - - 98012 RMVar_ID_98012 Human_SNP_ID_116991753 m1A Human chr2 + 232742648 232742648 232742648 GGATGCATTTGCAGCAGTCCAGGTGGGAAATAAAAGTGTGAATAAAAATTAGGTTAGTTGGATCA GGATGCATTTGCAGCAGTCCAGGTGGGAAATACAAGTGTGAATAAAAATTAGGTTAGTTGGATCA A C GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232742640..232742748 26863196 MeRIP-seq:(Medium) rs1410833274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_15946,RMVar_hsa_circ_308150,RMVar_hsa_circ_207656,RMVar_hsa_circ_377989,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658,RMVar_hsa_circ_207659,RMVar_hsa_circ_207661,RMVar_hsa_circ_71507,RMVar_hsa_circ_116493,RMVar_hsa_circ_337845,RMVar_hsa_circ_277743,RMVar_hsa_circ_304031,RMVar_hsa_circ_361789,RMVar_hsa_circ_368296,RMVar_hsa_circ_278241,RMVar_hsa_circ_20048,RMVar_hsa_circ_207663,RMVar_hsa_circ_207664,RMVar_hsa_circ_207665,RMVar_hsa_circ_207662 98013 RMVar_ID_98013 Human_SNP_ID_116991887 m1A Human chr2 - 232743188 232743188 232743188 AACGCAGTGTGCCTGGTTTCTCCTGCCACTCCACTAGCTCCTGCACTGTTCATCAATAACCTCAA AACGCAGTGTGCCTGGTTTCTCCTGCCACTCCGCTAGCTCCTGCACTGTTCATCAATAACCTCAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232743185..232743397 26863196 MeRIP-seq:(Medium) rs1265358417 Functional Loss SNV dbSNP153 33..33 33 - - - 98014 RMVar_ID_98014 Human_SNP_ID_117010030 m1A Human chr2 - 232815707 232815707 232815707 ACCTTTGCAGCTTTGGCCTTCTCTAGCTGCTGAAGCTGTTCCAGGGCAGGGCCTGGTGTCGTGGT ACCTTTGCAGCTTTGGCCTTCTCTAGCTGCTGCAGCTGTTCCAGGGCAGGGCCTGGTGTCGTGGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232811323..232815707 32194978 MeRIP-seq:(Medium) rs745849355 Functional Loss SNV dbSNP153 33..33 33 - - - 98015 RMVar_ID_98015 Human_SNP_ID_117010363 m1A Human chr2 + 232816963 232816963 232816963 AGGCAGGAAGAACTCCGAAGACAACAGGAGGAAATTCTTCGGCGACAGCAGGAAGAAGAAAGGAA AGGCAGGAAGAACTCCGAAGACAACAGGAGGAGATTCTTCGGCGACAGCAGGAAGAAGAAAGGAA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232816916..232817081 26863196 MeRIP-seq:(Medium) rs775978608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60568,Human_RBP_ID_919456,Human_RBP_ID_2627530,Human_RBP_ID_9347838,Human_RBP_ID_9385717,Human_RBP_ID_22815048,Human_RBP_ID_22996930,Human_RBP_ID_24545982,Human_RBP_ID_26341859,Human_RBP_ID_27818099 Human_Splice_Rec_371294,Human_Splice_Rec_371295,Human_Splice_Rec_371366,Human_Splice_Rec_371367,Human_Splice_Rec_371484,Human_Splice_Rec_371485,Human_Splice_Rec_371538,Human_Splice_Rec_371539,Human_Splice_Rec_371588,Human_Splice_Rec_371622,Human_Splice_Rec_371623,Human_Splice_Rec_371686,Human_Splice_Rec_371687,Human_Splice_Rec_371772,Human_Splice_Rec_371773,Human_Splice_Rec_371894,Human_Splice_Rec_371895 RMVar_hsa_circ_3560,RMVar_hsa_circ_353013,RMVar_hsa_circ_365156,RMVar_hsa_circ_367072,RMVar_hsa_circ_362037,RMVar_hsa_circ_56928,RMVar_hsa_circ_267140,RMVar_hsa_circ_68869,RMVar_hsa_circ_54996,RMVar_hsa_circ_59581,RMVar_hsa_circ_299799,RMVar_hsa_circ_349958,RMVar_hsa_circ_358387,RMVar_hsa_circ_287649,RMVar_hsa_circ_62161,RMVar_hsa_circ_43882,RMVar_hsa_circ_62712,RMVar_hsa_circ_70691,RMVar_hsa_circ_87635,RMVar_hsa_circ_207679 98016 RMVar_ID_98016 Human_SNP_ID_117011130 m1A Human chr2 + 232819909 232819909 232819909 GCGAGAAGAGGAAGAAAGACAGCAGCAAGAAGAAGCTCTTAGAAGACTGGAAGAGAGGAGAAGAG GCGAGAAGAGGAAGAAAGACAGCAGCAAGAAGCAGCTCTTAGAAGACTGGAAGAGAGGAGAAGAG A C GIGYF2 Ensembl:ENSG00000204120 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:232819876..232820016 26863196 MeRIP-seq:(Medium) rs1266908311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61803,Human_RBP_ID_206305,Human_RBP_ID_919459,Human_RBP_ID_1592312,Human_RBP_ID_6896434,Human_RBP_ID_8257505,Human_RBP_ID_9385719,Human_RBP_ID_22996932,Human_RBP_ID_23119363,Human_RBP_ID_24545984,Human_RBP_ID_26340452,Human_RBP_ID_27818101 Human_Splice_Rec_371296,Human_Splice_Rec_371297,Human_Splice_Rec_371368,Human_Splice_Rec_371369,Human_Splice_Rec_371486,Human_Splice_Rec_371487,Human_Splice_Rec_371540,Human_Splice_Rec_371541,Human_Splice_Rec_371624,Human_Splice_Rec_371625,Human_Splice_Rec_371688,Human_Splice_Rec_371689,Human_Splice_Rec_371774,Human_Splice_Rec_371896,Human_Splice_Rec_371897 RMVar_hsa_circ_3560,RMVar_hsa_circ_353013,RMVar_hsa_circ_365156,RMVar_hsa_circ_367072,RMVar_hsa_circ_362037,RMVar_hsa_circ_267140,RMVar_hsa_circ_68869,RMVar_hsa_circ_59581,RMVar_hsa_circ_75183,RMVar_hsa_circ_299799,RMVar_hsa_circ_349958,RMVar_hsa_circ_358387,RMVar_hsa_circ_287649,RMVar_hsa_circ_62161,RMVar_hsa_circ_43882,RMVar_hsa_circ_70691,RMVar_hsa_circ_357490,RMVar_hsa_circ_317686,RMVar_hsa_circ_56189,RMVar_hsa_circ_69343 98017 RMVar_ID_98017 Human_SNP_ID_117014193 m1A Human chr2 + 232832739 232832739 232832739 AGGTTACTTCTACCTTGCATCATCATGAACAGAGTTTCTGCTTTCTCTGTCATCTCTATAGCCAT AGGTTACTTCTACCTTGCATCATCATGAACAGCGTTTCTGCTTTCTCTGTCATCTCTATAGCCAT A C GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:232832738..232832900 26863196 MeRIP-seq:(Medium) rs1184737744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_365156,RMVar_hsa_circ_367072,RMVar_hsa_circ_362037,RMVar_hsa_circ_75183,RMVar_hsa_circ_299799,RMVar_hsa_circ_358387,RMVar_hsa_circ_287649,RMVar_hsa_circ_62161,RMVar_hsa_circ_43882,RMVar_hsa_circ_357490,RMVar_hsa_circ_56189,RMVar_hsa_circ_69343 98018 RMVar_ID_98018 Human_SNP_ID_117014250 m1A Human chr2 - 232832930 232832930 232832930 CCTCATGCCGGAGTCTGGCTGCCTCCTCTTCCATCCGCAGCCGGTTCTCCTCTAATCGACGCTGG CCTCATGCCGGAGTCTGGCTGCCTCCTCTTCCTTCCGCAGCCGGTTCTCCTCTAATCGACGCTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:232832809..232833050 26863196 MeRIP-seq:(Medium) rs909196736 Functional Loss SNV dbSNP153 33..33 33 - - - 98019 RMVar_ID_98019 Human_SNP_ID_117018381 m1A Human chr2 - 232847513 232847510 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGC___TGCTGCTGCTGACGCTGCTGGTTGGCTTTC AGCT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs748470696 Functional Loss DEL dbSNP153 33..35 33 - - - 98020 RMVar_ID_98020 Human_SNP_ID_117018384 m1A Human chr2 - 232847513 232847512 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGC_GCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs1455615084 Functional Loss DEL dbSNP153 33..33 33 - - - 98021 RMVar_ID_98021 Human_SNP_ID_117018385 m1A Human chr2 - 232847513 232847513 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCTGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs114013774 Functional Loss SNV dbSNP153 33..33 33 - - - 98022 RMVar_ID_98022 Human_SNP_ID_117018386 m1A Human chr2 - 232847513 232847513 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCGGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs114013774 Functional Loss SNV dbSNP153 33..33 33 - - - 98023 RMVar_ID_98023 Human_SNP_ID_117019493 m1A Human chr2 + 232851926 232851926 232851926 TTTGGTAGTGGGGATGAAAAGGAGTTAGATGGATTTCAGAAATGTAGGGGATAGAATTAACTGGA TTTGGTAGTGGGGATGAAAAGGAGTTAGATGGGTTTCAGAAATGTAGGGGATAGAATTAACTGGA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232851909..232852020 26863196 MeRIP-seq:(Medium) rs1416249096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23857448 98024 RMVar_ID_98024 Human_SNP_ID_117040929 m1A Human chr2 - 232928059 232928029 232928059 CCGCTCCGCAGCCCGCTAGTCGCCCCCGACCCAGCCCAGGGCCCCGGCGTGGCCCCCGACCCGGC CCGCTCCGCAGCCCGCTAGTCGCCCCCGACCC______________________________GGC CGGGTCGGGGGCCACGCCGGGGCCCTGGGCT C NGEF Ensembl:ENSG00000066248 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:232927951..232928125 26863410 MeRIP-seq:(Medium) rs1246780925 Functional Loss DEL dbSNP153 33..62 33 - - - RMVar_hsa_circ_73323 98025 RMVar_ID_98025 Human_SNP_ID_117126875 m1A Human chr2 + 233251766 233251765 233251766 CATTCCCGCTTCTGCTGGTTGCTTCATGCTGCAGGCTGCGGCCGTCAGCCCTCGCTCGCATTGGT CATTCCCGCTTCTGCTGGTTGCTTCATGCTGC_GGCTGCGGCCGTCAGCCCTCGCTCGCATTGGT CA C ATG16L1 Ensembl:ENSG00000085978 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:233251718..233251862 26863196 MeRIP-seq:(Medium) rs1559369952 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4623910,Human_RBP_ID_5471484,Human_RBP_ID_9385736,Human_RBP_ID_26340462 98026 RMVar_ID_98026 Human_SNP_ID_117137276 m1A Human chr2 - 233291016 233291016 233291016 TCCTCTACTGACTTGAACTTAGGTCCTTATCAACTCTATTGGTTTCCTATTCCCTAATATGCCCT TCCTCTACTGACTTGAACTTAGGTCCTTATCAGCTCTATTGGTTTCCTATTCCCTAATATGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:233290981..233291176 26863196 MeRIP-seq:(Medium) rs1359219383 Functional Loss SNV dbSNP153 33..33 33 - - - 98027 RMVar_ID_98027 Human_SNP_ID_117138446 m1A Human chr2 - 233295191 233295191 233295191 AGCACCAAGGGCATCGCACACAGGCTTGGCAGAGGGGCCATGGCCAGAATCACCACCTTCAGACA AGCACCAAGGGCATCGCACACAGGCTTGGCAGGGGGGCCATGGCCAGAATCACCACCTTCAGACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:233295140..233295224 32194978 MeRIP-seq:(Medium) rs1559420689 Functional Loss SNV dbSNP153 33..33 33 - - - 98028 RMVar_ID_98028 Human_SNP_ID_117165315 m1A Human chr2 + 233397130 233397130 233397130 GGAGCAGGGTGGCTGGCAGAGGCCAGAGTGAGAGGACACCAGAGGGGACCAGGGTGGCTGCGGGG GGAGCAGGGTGGCTGGCAGAGGCCAGAGTGAGGGGACACCAGAGGGGACCAGGGTGGCTGCGGGG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:233397077..233397191;chr2:233396773..233397203;chr2:233396792..233397916;chr2:233396827..233397179 26863196 MeRIP-seq:(Medium) rs1383033233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200864,Human_RBP_ID_23857770 RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98029 RMVar_ID_98029 Human_SNP_ID_117165459 m1A Human chr2 + 233397357 233397354 233397357 CACCAGAGGGGACCAGGGTGGCTGAGGGGGGCAGCAGAGTGAGAGGACTCCAGAGGGGACCAGGG CACCAGAGGGGACCAGGGTGGCTGAGGGGG___GCAGAGTGAGAGGACTCCAGAGGGGACCAGGG GGCA G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:233397271..233397904 26863196 MeRIP-seq:(Medium) rs1368075834 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8200866 RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98030 RMVar_ID_98030 Human_SNP_ID_117165462 m1A Human chr2 + 233397357 233397357 233397357 CACCAGAGGGGACCAGGGTGGCTGAGGGGGGCAGCAGAGTGAGAGGACTCCAGAGGGGACCAGGG CACCAGAGGGGACCAGGGTGGCTGAGGGGGGCGGCAGAGTGAGAGGACTCCAGAGGGGACCAGGG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:233397271..233397904 26863196 MeRIP-seq:(Medium) rs1388084507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200866 RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98031 RMVar_ID_98031 Human_SNP_ID_117165464 m1A Human chr2 + 233397360 233397358 233397360 CAGAGGGGACCAGGGTGGCTGAGGGGGGCAGCAGAGTGAGAGGACTCCAGAGGGGACCAGGGTGG CAGAGGGGACCAGGGTGGCTGAGGGGGGCAG__GAGTGAGAGGACTCCAGAGGGGACCAGGGTGG GCA G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:233397309..233397570 26863196 MeRIP-seq:(Medium) rs1475579967 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8200866 RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98032 RMVar_ID_98032 Human_SNP_ID_117165466 m1A Human chr2 + 233397360 233397359 233397361 CAGAGGGGACCAGGGTGGCTGAGGGGGGCAGCAGAGTGAGAGGACTCCAGAGGGGACCAGGGTGG CAGAGGGGACCAGGGTGGCTGAGGGGGGCAGC__AGTGAGAGGACTCCAGAGGGGACCAGGGTGG CAG C DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:233397309..233397570 26863196 MeRIP-seq:(Medium) rs200927104 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8200866 RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98033 RMVar_ID_98033 Human_SNP_ID_117172258 m1A Human chr2 + 233424655 233424655 233424655 CACCACCCAGATGAGGAGAGGCTGCGGGATGGAGGTCCAGGGCTCCGCCTGGAGCCCCCCTGCCT CACCACCCAGATGAGGAGAGGCTGCGGGATGGTGGTCCAGGGCTCCGCCTGGAGCCCCCCTGCCT A T DGKD Ensembl:ENSG00000077044 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:233424652..233424759 32194978 MeRIP-seq:(Medium) rs1309430351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 98034 RMVar_ID_98034 Human_SNP_ID_117177215 m1A Human chr2 + 233442159 233442159 233442159 GTGTGCAGTTTGGTGGCCAGGGCAGAGAGGGGAGAGCCTGGGCCACCCCCTGGCATTGTGGAGGC GTGTGCAGTTTGGTGGCCAGGGCAGAGAGGGGGGAGCCTGGGCCACCCCCTGGCATTGTGGAGGC A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:233442117..233442320 26863196 MeRIP-seq:(Medium) rs914478636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_81394,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_207730,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735 98035 RMVar_ID_98035 Human_SNP_ID_117177216 m1A Human chr2 + 233442159 233442159 233442159 GTGTGCAGTTTGGTGGCCAGGGCAGAGAGGGGAGAGCCTGGGCCACCCCCTGGCATTGTGGAGGC GTGTGCAGTTTGGTGGCCAGGGCAGAGAGGGGTGAGCCTGGGCCACCCCCTGGCATTGTGGAGGC A T DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:233442117..233442320 26863196 MeRIP-seq:(Medium) rs914478636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_81394,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_207730,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735 98036 RMVar_ID_98036 Human_SNP_ID_117178017 m1A Human chr2 - 233445136 233445136 233445136 GTATCACTTCTCTCCTCTAAATCCTATCCAAAAAAGGTGCCAGGACCATCCTCAGTCTGGAGGCT GTATCACTTCTCTCCTCTAAATCCTATCCAAAGAAGGTGCCAGGACCATCCTCAGTCTGGAGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:233445117..233445363 26863196 MeRIP-seq:(Medium) rs558443071 Functional Loss SNV dbSNP153 33..33 33 - - - 98037 RMVar_ID_98037 Human_SNP_ID_117178157 m1A Human chr2 + 233445739 233445739 233445739 CAGCTCCCCCAGATCTTGGAGAAGTTGGAGAGAGCCAGCACCAAGATGCTGGACAGGTGAGTGGG CAGCTCCCCCAGATCTTGGAGAAGTTGGAGAGCGCCAGCACCAAGATGCTGGACAGGTGAGTGGG A C DGKD Ensembl:ENSG00000077044 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:233445689..233446739 32194978 MeRIP-seq:(Medium) rs777022600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9104026,Human_RBP_ID_18756153,Human_RBP_ID_19000892,Human_RBP_ID_23119515 Human_Splice_Rec_372841,Human_Splice_Rec_372919,Human_Splice_Rec_372979,Human_Splice_Rec_373015 RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_81394,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_207730,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735 98038 RMVar_ID_98038 Human_SNP_ID_117178970 m1A Human chr2 + 233448364 233448364 233448364 AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCATGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCCTGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT A C DGKD Ensembl:ENSG00000077044 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:233448276..233448375;chr2:233448326..233448375;chr2:233448301..233448400 26863196 MeRIP-seq:(Medium) rs763411510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19000894,Human_RBP_ID_23119516 Human_Splice_Rec_372846,Human_Splice_Rec_372847,Human_Splice_Rec_372924,Human_Splice_Rec_372925,Human_Splice_Rec_372984,Human_Splice_Rec_372985,Human_Splice_Rec_373020,Human_Splice_Rec_373021,Human_Splice_Rec_373058,Human_Splice_Rec_373059,Human_Splice_Rec_373062,Human_Splice_Rec_373063 RMVar_hsa_circ_1183,RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_56119,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735,RMVar_hsa_circ_57387,RMVar_hsa_circ_19377,RMVar_hsa_circ_207736,RMVar_hsa_circ_376882 98039 RMVar_ID_98039 Human_SNP_ID_117178971 m1A Human chr2 + 233448364 233448364 233448364 AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCATGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCGTGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT A G DGKD Ensembl:ENSG00000077044 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:233448276..233448375;chr2:233448326..233448375;chr2:233448301..233448400 26863196 MeRIP-seq:(Medium) rs763411510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19000894,Human_RBP_ID_23119516 Human_Splice_Rec_372846,Human_Splice_Rec_372847,Human_Splice_Rec_372924,Human_Splice_Rec_372925,Human_Splice_Rec_372984,Human_Splice_Rec_372985,Human_Splice_Rec_373020,Human_Splice_Rec_373021,Human_Splice_Rec_373058,Human_Splice_Rec_373059,Human_Splice_Rec_373062,Human_Splice_Rec_373063 RMVar_hsa_circ_1183,RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_56119,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735,RMVar_hsa_circ_57387,RMVar_hsa_circ_19377,RMVar_hsa_circ_207736,RMVar_hsa_circ_376882 98040 RMVar_ID_98040 Human_SNP_ID_117178972 m1A Human chr2 + 233448364 233448364 233448364 AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCATGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT AGACGACCGAGAGCTCGGAGGAGTCAGAGGTCTTGGCCAAGAAGGTCTGTTCCCGTGCCCTGGGT A T DGKD Ensembl:ENSG00000077044 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:233448276..233448375;chr2:233448326..233448375;chr2:233448301..233448400 26863196 MeRIP-seq:(Medium) rs763411510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19000894,Human_RBP_ID_23119516 Human_Splice_Rec_372846,Human_Splice_Rec_372847,Human_Splice_Rec_372924,Human_Splice_Rec_372925,Human_Splice_Rec_372984,Human_Splice_Rec_372985,Human_Splice_Rec_373020,Human_Splice_Rec_373021,Human_Splice_Rec_373058,Human_Splice_Rec_373059,Human_Splice_Rec_373062,Human_Splice_Rec_373063 RMVar_hsa_circ_1183,RMVar_hsa_circ_99963,RMVar_hsa_circ_207722,RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_97802,RMVar_hsa_circ_59849,RMVar_hsa_circ_101384,RMVar_hsa_circ_37211,RMVar_hsa_circ_207729,RMVar_hsa_circ_92939,RMVar_hsa_circ_207732,RMVar_hsa_circ_56119,RMVar_hsa_circ_32498,RMVar_hsa_circ_207735,RMVar_hsa_circ_57387,RMVar_hsa_circ_19377,RMVar_hsa_circ_207736,RMVar_hsa_circ_376882 98041 RMVar_ID_98041 Human_SNP_ID_117183621 m1A Human chr2 + 233463375 233463375 233463375 CGCATCTCACTCCACACATCACCTCACTCCACACATCTCCTCACTCCACACATCTCCTCACTCCA CGCATCTCACTCCACACATCACCTCACTCCACGCATCTCCTCACTCCACACATCTCCTCACTCCA A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:233463325..233463413 26863196 MeRIP-seq:(Medium) rs1255106564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205531,Human_RBP_ID_2627948 RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_32498,RMVar_hsa_circ_32447 98042 RMVar_ID_98042 Human_SNP_ID_117183797 m1A Human chr2 + 233463674 233463674 233463674 TCCACGCATGTCCTCACTGCACGCATCTCCTCACTCCACGCATCACCTCACTCCACGCATCACCT TCCACGCATGTCCTCACTGCACGCATCTCCTCGCTCCACGCATCACCTCACTCCACGCATCACCT A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:233463669..233463753 26863196 MeRIP-seq:(Medium) rs1368107711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_204965,Human_RBP_ID_1067780,Human_RBP_ID_2627953,Human_RBP_ID_24533563,Human_RBP_ID_26760636,Human_RBP_ID_26787436 RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_32498,RMVar_hsa_circ_32447 98043 RMVar_ID_98043 Human_SNP_ID_117183819 m1A Human chr2 - 233463701 233463701 233463701 GCGTAGAGTGAGGATTTCTGTGGAGTGAGGTGATGCGTGGAGTGAGGTGATGCGTGGAGTGAGGA GCGTAGAGTGAGGATTTCTGTGGAGTGAGGTGTTGCGTGGAGTGAGGTGATGCGTGGAGTGAGGA T A lnc-USP40-2 RNACentral:URS00008C0F05 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:233463651..233463759 26863196 MeRIP-seq:(Medium) rs1348092684 Functional Loss SNV dbSNP153 33..33 33 - - - 98044 RMVar_ID_98044 Human_SNP_ID_117185480 m1A Human chr2 - 233469535 233469535 233469535 TCTGCCCAGGGCCTCAGTGGCAGGAGGCGCAGAGGCCACAGGCTGAGAGGGCGGAGGCTAGGCCT TCTGCCCAGGGCCTCAGTGGCAGGAGGCGCAGGGGCCACAGGCTGAGAGGGCGGAGGCTAGGCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:233469466..233469612 32194978 MeRIP-seq:(Medium) rs891491522 Functional Loss SNV dbSNP153 33..33 33 - - - 98045 RMVar_ID_98045 Human_SNP_ID_117186125 m1A Human chr2 + 233471556 233471556 233471556 AGCTGGAACTTGGGTGGGGAGGGGACATGAGGAGGATAAACAGCTGACTGTGGCTTCAAGGACAT AGCTGGAACTTGGGTGGGGAGGGGACATGAGGCGGATAAACAGCTGACTGTGGCTTCAAGGACAT A C DGKD Ensembl:ENSG00000077044 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:233471425..233471588 26863196 MeRIP-seq:(Medium) rs551286995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60775,Human_RBP_ID_8514230,Human_RBP_ID_18167334 98046 RMVar_ID_98046 Human_SNP_ID_117209774 m1A Human chr2 + 233566625 233566625 233566625 TCTCGCCTCGCCCTCCTCAGACTGGGCCACCAACACTGTCCCTACGCTTCCCACGTCCCTCCCAG TCTCGCCTCGCCCTCCTCAGACTGGGCCACCACCACTGTCCCTACGCTTCCCACGTCCCTCCCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:233566602..233566702;chr2:233566619..233566747 26863196 MeRIP-seq:(Medium) rs1378866933 Functional Loss SNV dbSNP153 33..33 33 - - - 98047 RMVar_ID_98047 Human_SNP_ID_117282312 m1A Human chr2 - 233841121 233841121 233841121 CACGTTCAGGGAAATAGTTCTGGAATATTTAGAAAGTCAGTGTCACCCAGCAAAACTCTTTCAGT CACGTTCAGGGAAATAGTTCTGGAATATTTAGGAAGTCAGTGTCACCCAGCAAAACTCTTTCAGT T C HJURP Ensembl:ENSG00000123485 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:233841075..233841176 32194978 MeRIP-seq:(Medium) rs1192100614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546115,Human_RBP_ID_1912920,Human_RBP_ID_13803649,Human_RBP_ID_17275453,Human_RBP_ID_22076898 98048 RMVar_ID_98048 Human_SNP_ID_117282432 m1A Human chr2 + 233841421 233841421 233841421 ATGGCCCAGGAGTCCGGGAGGCACATCCGGCGAGGCTGGTTCCTGGGACTCAGGCAATATTCCCG ATGGCCCAGGAGTCCGGGAGGCACATCCGGCGGGGCTGGTTCCTGGGACTCAGGCAATATTCCCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:233841373..233841523 32194978 MeRIP-seq:(Medium) rs775094252 Functional Loss SNV dbSNP153 33..33 33 - - - 98049 RMVar_ID_98049 Human_SNP_ID_117285941 m1A Human chr2 - 233854475 233854475 233854475 GGGTCCGATGCTGGGTACGCTGCGCGCCATGGAGGGCGAGGACGTGGAAGACGACCAGCTGCTGC GGGTCCGATGCTGGGTACGCTGCGCGCCATGGTGGGCGAGGACGTGGAAGACGACCAGCTGCTGC T A HJURP Ensembl:ENSG00000123485 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr2:233854359..233854525;chr2:233854426..233854525 26863196 MeRIP-seq:(Medium) rs774050082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61114,Human_RBP_ID_4623911,Human_RBP_ID_5146968,Human_RBP_ID_6897175,Human_RBP_ID_9330841,Human_RBP_ID_9385762,Human_RBP_ID_18422044,Human_RBP_ID_22478127,Human_RBP_ID_22996935,Human_RBP_ID_23857968 Human_Splice_Rec_373707,Human_Splice_Rec_373717,Human_Splice_Rec_373729,Human_Splice_Rec_373745,Human_Splice_Rec_373753,Human_Splice_Rec_373767 98050 RMVar_ID_98050 Human_SNP_ID_117285955 m1A Human chr2 + 233854499 233854499 233854499 CCTCGCCCTCCATGGCGCGCAGCGTACCCAGCATCGGACCCAGCCAGTACCCAAGCGCCAACCCG CCTCGCCCTCCATGGCGCGCAGCGTACCCAGCGTCGGACCCAGCCAGTACCCAAGCGCCAACCCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:233854170..233854525 26863196 MeRIP-seq:(Medium) rs758541868 Functional Loss SNV dbSNP153 33..33 33 - - - 98051 RMVar_ID_98051 Human_SNP_ID_117289180 m1A Human chr2 - 233867267 233867267 233867267 CCTCTGACAGTAGTGAAGACAAGGATGAAAAAATAAGTGAAGAATGTGATATTGAAGAAAAGACT CCTCTGACAGTAGTGAAGACAAGGATGAAAAAGTAAGTGAAGAATGTGATATTGAAGAAAAGACT T C MSL3P1,AC005538.2 Ensembl:ENSG00000224287,Ensembl:ENSG00000279809 Pseudogene,Other exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:233867216..233867296 26863196 MeRIP-seq:(Medium) rs1369050333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205954,Human_RBP_ID_5099586,Human_RBP_ID_5589739,Human_RBP_ID_26341879 Human_Splice_Rec_373782 Human_miRNA_ID_1824472,Human_miRNA_ID_1844819,Human_miRNA_ID_1845285,Human_miRNA_ID_1845762,Human_miRNA_ID_3151137,Human_miRNA_ID_3164908,Human_miRNA_ID_3165061,Human_miRNA_ID_3165214 98052 RMVar_ID_98052 Human_SNP_ID_117565984 m1A Human chr2 + 234951978 234951972 234951978 CCCCGCCCCCGCCCCCGCCCCCGCCCCCGCCCAGGCGCGGGACCACCCTCCGCCCGCCGAGGCGG CCCCGCCCCCGCCCCCGCCCCCGCCCC______GGCGCGGGACCACCCTCCGCCCGCCGAGGCGG CCGCCCA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:234951851..234952190 26863196 MeRIP-seq:(Medium) rs1415405666 Functional Loss DEL dbSNP153 28..33 33 - - - 98053 RMVar_ID_98053 Human_SNP_ID_117565989 m1A Human chr2 + 234951978 234951978 234951978 CCCCGCCCCCGCCCCCGCCCCCGCCCCCGCCCAGGCGCGGGACCACCCTCCGCCCGCCGAGGCGG CCCCGCCCCCGCCCCCGCCCCCGCCCCCGCCCCGGCGCGGGACCACCCTCCGCCCGCCGAGGCGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:234951851..234952190 26863196 MeRIP-seq:(Medium) rs1157094887 Functional Loss SNV dbSNP153 33..33 33 - - - 98054 RMVar_ID_98054 Human_SNP_ID_117566065 m1A Human chr2 - 234952121 234952121 234952121 CCCGCCGGCTCCTGAGGCTCCGCTCGTCGGCCAGCGGCTCGGCCCAGCCGGGGGCGCGCGCGGCT CCCGCCGGCTCCTGAGGCTCCGCTCGTCGGCCGGCGGCTCGGCCCAGCCGGGGGCGCGCGCGGCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:234952072..234952212 26863196 MeRIP-seq:(Medium) rs1483691077 Functional Loss SNV dbSNP153 33..33 33 - - - 98055 RMVar_ID_98055 Human_SNP_ID_117566082 m1A Human chr2 - 234952161 234952161 234952161 GCTCCCCGCCGCCGCCTGCCTACCTGGCTCGCATGGCGTCCCCGCCGGCTCCTGAGGCTCCGCTC GCTCCCCGCCGCCGCCTGCCTACCTGGCTCGCTTGGCGTCCCCGCCGGCTCCTGAGGCTCCGCTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:234952025..234953102;chr2:234952026..234953070 26863196 MeRIP-seq:(Medium) rs943822378 Functional Loss SNV dbSNP153 33..33 33 - - - 98056 RMVar_ID_98056 Human_SNP_ID_117566342 m1A Human chr2 - 234952977 234952977 234952977 GCGCGGCATCTCTGGGCGCCCGACACCCGGTCAGGGCCAGCTGGGCCTGTCCCCAACCCCCGTCT GCGCGGCATCTCTGGGCGCCCGACACCCGGTCTGGGCCAGCTGGGCCTGTCCCCAACCCCCGTCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:234952971..234953048 26863196 MeRIP-seq:(Medium) rs1026450357 Functional Loss SNV dbSNP153 33..33 33 - - - 98057 RMVar_ID_98057 Human_SNP_ID_117580024 m1A Human chr2 + 235007172 235007172 235007172 GAGGGAGTGGAGGCAGTTGAGTGGGAGAGTCCAGGTGAGACAGGTGAGTCCCTGCAGGAAGGCAG GAGGGAGTGGAGGCAGTTGAGTGGGAGAGTCCGGGTGAGACAGGTGAGTCCCTGCAGGAAGGCAG A G SH3BP4 Ensembl:ENSG00000130147 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235007170..235007318 26863196 MeRIP-seq:(Medium) rs1250568710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200881,Human_RBP_ID_23282850,Human_RBP_ID_26787449 RMVar_hsa_circ_207755,RMVar_hsa_circ_317246,RMVar_hsa_circ_352523 98058 RMVar_ID_98058 Human_SNP_ID_117580157 m1A Human chr2 - 235007724 235007701 235007725 GGATGGCCGCAGCCCGGGCTCAGGATGGCCGCAGCCTCTCAAGCACTGCACGCCTGGTCTCTTCT GGATGGCCGCAGCCCGGGCTCAGGATGGCCG________________________GGTCTCTTCT CAGGCGTGCAGTGCTTGAGAGGCTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235007721..235008023 26863196 MeRIP-seq:(Medium) rs1200191264 Functional Loss DEL dbSNP153 32..55 33 - - - 98059 RMVar_ID_98059 Human_SNP_ID_117584781 m1A Human chr2 - 235025817 235025817 235025817 CTATAACATCAAAACCTACCGATTGGAGAATGACCCCCTGAAACAGTGCCTTTGCCTTTGCAAAT CTATAACATCAAAACCTACCGATTGGAGAATGTCCCCCTGAAACAGTGCCTTTGCCTTTGCAAAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235025806..235025974 26863196 MeRIP-seq:(Medium) rs117816034 Functional Loss SNV dbSNP153 33..33 33 - - - 98060 RMVar_ID_98060 Human_SNP_ID_117585620 m1A Human chr2 + 235029132 235029132 235029132 AGAGGAGCTGATGACTGTAATTGCATCGAGAGATGACGGTGGTGTGGATGTGCTGGGGAGAGGTC AGAGGAGCTGATGACTGTAATTGCATCGAGAGGTGACGGTGGTGTGGATGTGCTGGGGAGAGGTC A G SH3BP4 Ensembl:ENSG00000130147 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235029122..235029315 26863196 MeRIP-seq:(Medium) rs1359256934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207755,RMVar_hsa_circ_317246,RMVar_hsa_circ_352523 98061 RMVar_ID_98061 Human_SNP_ID_117591361 m1A Human chr2 - 235047796 235047796 235047796 AACTTGACCAAAACGCCCCTGCTACAGCCATCACCGACGGCTCCAGGTCACCACACCCCACGGCT AACTTGACCAAAACGCCCCTGCTACAGCCATCGCCGACGGCTCCAGGTCACCACACCCCACGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235047793..235048010 26863196 MeRIP-seq:(Medium) rs1262555503 Functional Loss SNV dbSNP153 33..33 33 - - - 98062 RMVar_ID_98062 Human_SNP_ID_117593426 m1A Human chr2 + 235055516 235055516 235055516 AGAGACCATCTATCACCTTTTCCCCAAAGAAGAAACAAAACCAGTTGCACCTTAAACCATGGATA AGAGACCATCTATCACCTTTTCCCCAAAGAAGGAACAAAACCAGTTGCACCTTAAACCATGGATA A G SH3BP4 Ensembl:ENSG00000130147 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:235055476..235055575 26863196 MeRIP-seq:(Medium) rs1049378931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17509840 98063 RMVar_ID_98063 Human_SNP_ID_117707461 m1A Human chr2 - 235494114 235494114 235494114 GCCGACCTGGGACCGAGTCGCAGGCGCCTTGCAAGCCGCGGAGCCCGCTCCGAGCGCCGCCCGCC GCCGACCTGGGACCGAGTCGCAGGCGCCTTGCGAGCCGCGGAGCCCGCTCCGAGCGCCGCCCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235493952..235494253 26863196 MeRIP-seq:(Medium) rs890620813 Functional Loss SNV dbSNP153 33..33 33 - - - 98064 RMVar_ID_98064 Human_SNP_ID_117707471 m1A Human chr2 + 235494139 235494139 235494139 CGCGGCTTGCAAGGCGCCTGCGACTCGGTCCCAGGTCGGCGGGCGGCGCACGGCGGGCTCGCGCG CGCGGCTTGCAAGGCGCCTGCGACTCGGTCCCGGGTCGGCGGGCGGCGCACGGCGGGCTCGCGCG A G AGAP1 Ensembl:ENSG00000157985 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:235494056..235494201 26863196 MeRIP-seq:(Medium) rs1476784277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622997,Human_RBP_ID_9330842,Human_RBP_ID_22597270 RMVar_hsa_circ_98432,RMVar_hsa_circ_110051,RMVar_hsa_circ_207759,RMVar_hsa_circ_207760 98065 RMVar_ID_98065 Human_SNP_ID_117707506 m1A Human chr2 + 235494228 235494228 235494228 CAGTACGCAGCGCGCGGACCCACGCCACGGCCAGGAGCCCAGAGCAGCGCGGCCACACTGCCCAG CAGTACGCAGCGCGCGGACCCACGCCACGGCCGGGAGCCCAGAGCAGCGCGGCCACACTGCCCAG A G AGAP1 Ensembl:ENSG00000157985 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:235493962..235494247 26863196 MeRIP-seq:(Medium) rs979944276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422524 RMVar_hsa_circ_98432,RMVar_hsa_circ_110051,RMVar_hsa_circ_207759,RMVar_hsa_circ_207760 98066 RMVar_ID_98066 Human_SNP_ID_117709420 m1A Human chr2 - 235500702 235500702 235500702 AGCATTCAGCTGCTTTTCAAACAGCATCATGAAGATCACATGAACACCAGCTTGAAACCATTCAG AGCATTCAGCTGCTTTTCAAACAGCATCATGAGGATCACATGAACACCAGCTTGAAACCATTCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235500700..235500838 26863196 MeRIP-seq:(Medium) rs1207813416 Functional Loss SNV dbSNP153 33..33 33 - - - 98067 RMVar_ID_98067 Human_SNP_ID_117712567 m1A Human chr2 - 235511907 235511906 235511908 ATACACATTCACACATTCACACACATCCACATACTCATTCACACTCACATTCACACACATTCACA ATACACATTCACACATTCACACACATCCACA__CTCATTCACACTCACATTCACACACATTCACA GTA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235511857..235512053 26863196 MeRIP-seq:(Medium) rs1379174219 Functional Loss DEL dbSNP153 32..33 33 - - - 98068 RMVar_ID_98068 Human_SNP_ID_117712569 m1A Human chr2 - 235511907 235511907 235511907 ATACACATTCACACATTCACACACATCCACATACTCATTCACACTCACATTCACACACATTCACA ATACACATTCACACATTCACACACATCCACATTCTCATTCACACTCACATTCACACACATTCACA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235511857..235512053 26863196 MeRIP-seq:(Medium) rs372635703 Functional Loss SNV dbSNP153 33..33 33 - - - 98069 RMVar_ID_98069 Human_SNP_ID_117719794 m1A Human chr2 + 235537244 235537244 235537244 AGAGCGGGGGTGGTGTGAATGTGTGTGGGTGCAGGGGCACCTCGGGAGCCTGGCCGGGAAGGTGG AGAGCGGGGGTGGTGTGAATGTGTGTGGGTGCGGGGGCACCTCGGGAGCCTGGCCGGGAAGGTGG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235537220..235537358 26863196 MeRIP-seq:(Medium) rs1246243620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_204987,Human_RBP_ID_264282,Human_RBP_ID_1067789,Human_RBP_ID_3638315,Human_RBP_ID_5239750,Human_RBP_ID_8200886,Human_RBP_ID_8514377,Human_RBP_ID_9331322,Human_RBP_ID_9429005,Human_RBP_ID_17141456,Human_RBP_ID_18422532,Human_RBP_ID_18493809,Human_RBP_ID_22699874,Human_RBP_ID_23119364,Human_RBP_ID_23282861,Human_RBP_ID_24533574,Human_RBP_ID_26786482 RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 98070 RMVar_ID_98070 Human_SNP_ID_117723297 m1A Human chr2 - 235549831 235549831 235549831 ACTCCACTAATCCCCATGCTCCCGGGGATGTTAGGCCGCGGTGAGATGCAACTAGGATGTTGTCT ACTCCACTAATCCCCATGCTCCCGGGGATGTTGGGCCGCGGTGAGATGCAACTAGGATGTTGTCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235549804..235549957 26863196 MeRIP-seq:(Medium) rs1353354300 Functional Loss SNV dbSNP153 33..33 33 - - - 98071 RMVar_ID_98071 Human_SNP_ID_117735190 m1A Human chr2 + 235592247 235592247 235592247 GAGGCTCCTCCTCCACTGCCCTGGCCACCTGGATGCTGCATTTAATTCTGGGCACCACGCGCCAG GAGGCTCCTCCTCCACTGCCCTGGCCACCTGGGTGCTGCATTTAATTCTGGGCACCACGCGCCAG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235592242..235592307 26863196 MeRIP-seq:(Medium) rs1351288560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_107898,RMVar_hsa_circ_207760,RMVar_hsa_circ_207762 98072 RMVar_ID_98072 Human_SNP_ID_117747657 m1A Human chr2 + 235637648 235637648 235637648 AAAGTTCGGACCAGTGGGCTGTATGTTTCAGAACTTTACACATAGGAAGAGGAAGTATTGTGTAT AAAGTTCGGACCAGTGGGCTGTATGTTTCAGATCTTTACACATAGGAAGAGGAAGTATTGTGTAT A T AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235637645..235637798 26863196 MeRIP-seq:(Medium) rs76461429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22990555 RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 98073 RMVar_ID_98073 Human_SNP_ID_117753397 m1A Human chr2 - 235658508 235658508 235658508 GCTCCACACCTCCTCCCAGACTCTTGACCTCGACCCCCGGGAGGCTGCAGGAAAGTCTTTCAAGT GCTCCACACCTCCTCCCAGACTCTTGACCTCGGCCCCCGGGAGGCTGCAGGAAAGTCTTTCAAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235658501..235658656 26863196 MeRIP-seq:(Medium) rs1261606182 Functional Loss SNV dbSNP153 33..33 33 - - - 98074 RMVar_ID_98074 Human_SNP_ID_117756571 m1A Human chr2 - 235670235 235670235 235670235 CCGCCGAACCGGGCGTGGGTCCGGGCCGCCGGAGCCCGGCGCGGCCAGCTGCTCCTTCCTGACCA CCGCCGAACCGGGCGTGGGTCCGGGCCGCCGGGGCCCGGCGCGGCCAGCTGCTCCTTCCTGACCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:235670222..235670326 32194978 MeRIP-seq:(Medium) rs1156499807 Functional Loss SNV dbSNP153 33..33 33 - - - 98075 RMVar_ID_98075 Human_SNP_ID_117756779 m1A Human chr2 - 235670646 235670646 235670646 GGTCCCGGCCGCGGCCTCGTCGCACGGCGCCCAGGCCAGGCTCCCGGAGCTGCTGTGGCGCCTTC GGTCCCGGCCGCGGCCTCGTCGCACGGCGCCCGGGCCAGGCTCCCGGAGCTGCTGTGGCGCCTTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:235670625..235670731 32194978 MeRIP-seq:(Medium) rs1477408086 Functional Loss SNV dbSNP153 33..33 33 - - - 98076 RMVar_ID_98076 Human_SNP_ID_117770394 m1A Human chr2 - 235714336 235714335 235714336 CCCGTCCTACCCCCACACTCCCAGCCAAACTCATATGTTGAAACCTAACCCCTGGCTGGGCATGG CCCGTCCTACCCCCACACTCCCAGCCAAACTC_TATGTTGAAACCTAACCCCTGGCTGGGCATGG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235714334..235714429 26863196 MeRIP-seq:(Medium) rs1299123132 Functional Loss DEL dbSNP153 33..33 33 - - - 98077 RMVar_ID_98077 Human_SNP_ID_117770396 m1A Human chr2 - 235714336 235714336 235714336 CCCGTCCTACCCCCACACTCCCAGCCAAACTCATATGTTGAAACCTAACCCCTGGCTGGGCATGG CCCGTCCTACCCCCACACTCCCAGCCAAACTCTTATGTTGAAACCTAACCCCTGGCTGGGCATGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235714334..235714429 26863196 MeRIP-seq:(Medium) rs1388247104 Functional Loss SNV dbSNP153 33..33 33 - - - 98078 RMVar_ID_98078 Human_SNP_ID_117770403 m1A Human chr2 + 235714361 235714361 235714361 CAACATATGAGTTTGGCTGGGAGTGTGGGGGTAGGACGGGGAAGCACAAACATTCCTACCATATA CAACATATGAGTTTGGCTGGGAGTGTGGGGGTGGGACGGGGAAGCACAAACATTCCTACCATATA A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:235714354..235714562 26863196 MeRIP-seq:(Medium) rs1044533817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6959,RMVar_hsa_circ_98432,RMVar_hsa_circ_207760,RMVar_hsa_circ_316372,RMVar_hsa_circ_330369,RMVar_hsa_circ_362517,RMVar_hsa_circ_322632,RMVar_hsa_circ_44106,RMVar_hsa_circ_286163,RMVar_hsa_circ_29046,RMVar_hsa_circ_207763,RMVar_hsa_circ_207764,RMVar_hsa_circ_207765 98079 RMVar_ID_98079 Human_SNP_ID_117770998 m1A Human chr2 - 235716397 235716397 235716397 CTACCAGGAAACTGCCCACTAGGTCACCCGCAACTTCCATTTCAAAGCCACTAGCCTGTCTCGCT CTACCAGGAAACTGCCCACTAGGTCACCCGCAGCTTCCATTTCAAAGCCACTAGCCTGTCTCGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235716391..235716475 26863196 MeRIP-seq:(Medium) rs1159859401 Functional Loss SNV dbSNP153 33..33 33 - - - 98080 RMVar_ID_98080 Human_SNP_ID_117796180 m1A Human chr2 + 235803001 235803001 235803001 TGGTTGTGGTTGTGATGGTTGTGATGGTGGTGATGGTTGTGGTTGTGATGGTGGTGATGGTTGTG TGGTTGTGGTTGTGATGGTTGTGATGGTGGTGGTGGTTGTGGTTGTGATGGTGGTGATGGTTGTG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235802596..235803225 26863196 MeRIP-seq:(Medium) rs978665773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5294148,Human_RBP_ID_23891992 RMVar_hsa_circ_98432,RMVar_hsa_circ_207760,RMVar_hsa_circ_330369,RMVar_hsa_circ_322632,RMVar_hsa_circ_44106,RMVar_hsa_circ_28906,RMVar_hsa_circ_207763,RMVar_hsa_circ_91320,RMVar_hsa_circ_17639,RMVar_hsa_circ_207768,RMVar_hsa_circ_344448,RMVar_hsa_circ_300207,RMVar_hsa_circ_60410,RMVar_hsa_circ_93779,RMVar_hsa_circ_207770,RMVar_hsa_circ_7507,RMVar_hsa_circ_84214,RMVar_hsa_circ_207776,RMVar_hsa_circ_321514,RMVar_hsa_circ_207771,RMVar_hsa_circ_207772,RMVar_hsa_circ_332313,RMVar_hsa_circ_370048,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_332938,RMVar_hsa_circ_207773,RMVar_hsa_circ_323537,RMVar_hsa_circ_279328,RMVar_hsa_circ_207781,RMVar_hsa_circ_207782 98081 RMVar_ID_98081 Human_SNP_ID_117796211 m1A Human chr2 - 235803029 235803029 235803029 CCACCATCACCACAACCATCATCACCATCACAACCATCACCACCATCACAACCACAACCATCACC CCACCATCACCACAACCATCATCACCATCACAGCCATCACCACCATCACAACCACAACCATCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:235802610..235803225;chr2:235802630..235803189 26863196 MeRIP-seq:(Medium) rs760484700 Functional Loss SNV dbSNP153 33..33 33 - - - 98082 RMVar_ID_98082 Human_SNP_ID_117802030 m1A Human chr2 + 235822567 235822567 235822567 GCTGAAGAAGCTCAAGGGTGAGGAGGAGCTGGAGAAGCCCAAGGGTGAAGAGAAGCTGGAGAAGC GCTGAAGAAGCTCAAGGGTGAGGAGGAGCTGGGGAAGCCCAAGGGTGAAGAGAAGCTGGAGAAGC A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235822318..235822815 26863196 MeRIP-seq:(Medium) rs1298857387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22597325 RMVar_hsa_circ_330369,RMVar_hsa_circ_44106,RMVar_hsa_circ_207763,RMVar_hsa_circ_91320,RMVar_hsa_circ_17639,RMVar_hsa_circ_207768,RMVar_hsa_circ_344448,RMVar_hsa_circ_60410,RMVar_hsa_circ_7507,RMVar_hsa_circ_84214,RMVar_hsa_circ_207772,RMVar_hsa_circ_332313,RMVar_hsa_circ_370048,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_332938,RMVar_hsa_circ_207773,RMVar_hsa_circ_323537,RMVar_hsa_circ_207782 98083 RMVar_ID_98083 Human_SNP_ID_117813624 m1A Human chr2 + 235865267 235865267 235865267 CTGGCCGAATCCAGTCCCGGCCGGCGCTTTGAAGCCTGTGCTGTGCGATTTTCTCAGCAGTGAGG CTGGCCGAATCCAGTCCCGGCCGGCGCTTTGAGGCCTGTGCTGTGCGATTTTCTCAGCAGTGAGG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235865250..235865415 26863196 MeRIP-seq:(Medium) rs1462746916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330369,RMVar_hsa_circ_44106,RMVar_hsa_circ_207763,RMVar_hsa_circ_17639,RMVar_hsa_circ_344448,RMVar_hsa_circ_60410,RMVar_hsa_circ_7507,RMVar_hsa_circ_84214,RMVar_hsa_circ_207772,RMVar_hsa_circ_332313,RMVar_hsa_circ_370048,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_332938,RMVar_hsa_circ_207773,RMVar_hsa_circ_323537,RMVar_hsa_circ_207782 98084 RMVar_ID_98084 Human_SNP_ID_117840721 m1A Human chr2 + 235962317 235962317 235962317 TCTCCCAGCCCTGGCCCATGACGGTGCTGAGCAGGTGGAGGGCTGGAAGTCAGTGAAGTTGGGGC TCTCCCAGCCCTGGCCCATGACGGTGCTGAGCGGGTGGAGGGCTGGAAGTCAGTGAAGTTGGGGC A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235962314..235962401 26863196 MeRIP-seq:(Medium) rs754103852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_17639,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207774,RMVar_hsa_circ_207773,RMVar_hsa_circ_50093,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_332067,RMVar_hsa_circ_207787,RMVar_hsa_circ_271275,RMVar_hsa_circ_207788 98085 RMVar_ID_98085 Human_SNP_ID_117850756 m1A Human chr2 + 235999167 235999161 235999167 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGATGATAATGGTGATGGTGATGATGGCAGTG GGTGACGATGGTGAGAGGTGGTGGTGG______TGATGATAATGGTGATGGTGATGATGGCAGTG GTGATGA G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235998658..235999509 26863196 MeRIP-seq:(Medium) rs141864400 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98086 RMVar_ID_98086 Human_SNP_ID_117850757 m1A Human chr2 + 235999167 235999161 235999167 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGATGATAATGGTGATGGTGATGATGGCAGTG GGTGACGATGGTGAGAGGTGGTGGTGGTGA___TGATGATAATGGTGATGGTGATGATGGCAGTG GTGATGA GTGA AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235998658..235999509 26863196 MeRIP-seq:(Medium) rs141864400 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98087 RMVar_ID_98087 Human_SNP_ID_117850760 m1A Human chr2 + 235999167 235999167 235999167 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGATGATAATGGTGATGGTGATGATGGCAGTG GGTGACGATGGTGAGAGGTGGTGGTGGTGATGGTGATGATAATGGTGATGGTGATGATGGCAGTG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235998658..235999509 26863196 MeRIP-seq:(Medium) rs1462916977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98088 RMVar_ID_98088 Human_SNP_ID_117851035 m1A Human chr2 + 235999669 235999652 235999670 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGGTGGTGGTGGTGGTCGTGGTGGTGATGATA GGTGACGATGGTGAGA__________________GGTGGTGGTGGTGGTCGTGGTGGTGATGATA AGGTGGTGGTGGTGATGAT A AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235999626..235999823 26863196 MeRIP-seq:(Medium) rs1467188550 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_827148,Human_RBP_ID_5294466,Human_RBP_ID_5651728,Human_RBP_ID_8200907,Human_RBP_ID_17141575,Human_RBP_ID_17279392,Human_RBP_ID_21981971,Human_RBP_ID_23114954,Human_RBP_ID_27840166 RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98089 RMVar_ID_98089 Human_SNP_ID_117851038 m1A Human chr2 + 235999669 235999654 235999669 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGGTGGTGGTGGTGGTCGTGGTGGTGATGATA GGTGACGATGGTGAGAGG_______________TGGTGGTGGTGGTGGTCGTGGTGGTGATGATA GTGGTGGTGGTGATGA G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235999626..235999823 26863196 MeRIP-seq:(Medium) rs1385784076 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_827148,Human_RBP_ID_5294466,Human_RBP_ID_5651728,Human_RBP_ID_8200907,Human_RBP_ID_17141575,Human_RBP_ID_17279392,Human_RBP_ID_21981971,Human_RBP_ID_23114954,Human_RBP_ID_27840166 RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98090 RMVar_ID_98090 Human_SNP_ID_117851051 m1A Human chr2 + 235999669 235999669 235999669 GGTGACGATGGTGAGAGGTGGTGGTGGTGATGATGGTGGTGGTGGTGGTCGTGGTGGTGATGATA GGTGACGATGGTGAGAGGTGGTGGTGGTGATGGTGGTGGTGGTGGTGGTCGTGGTGGTGATGATA A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235999626..235999823 26863196 MeRIP-seq:(Medium) rs532376451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827148,Human_RBP_ID_5294466,Human_RBP_ID_5651728,Human_RBP_ID_8200907,Human_RBP_ID_17141575,Human_RBP_ID_17279392,Human_RBP_ID_21981971,Human_RBP_ID_23114954,Human_RBP_ID_27840166 RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98091 RMVar_ID_98091 Human_SNP_ID_117851532 m1A Human chr2 + 236001117 236001117 236001117 GGGGAGGGGATGGACCCTCAGAGGCGAGACGGACGTACAGGAAACACCACATGGAGACTCTGGCG GGGGAGGGGATGGACCCTCAGAGGCGAGACGGGCGTACAGGAAACACCACATGGAGACTCTGGCG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:236001107..236001182 26863196 MeRIP-seq:(Medium) rs541761942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 98092 RMVar_ID_98092 Human_SNP_ID_117865414 m1A Human chr2 + 236051422 236051422 236051422 GGATGCCAGGGCTCGGGAGGGTGCATTCTGGGAGGTGTCACTGGAGAAATGGCATCTGAGCTGGA GGATGCCAGGGCTCGGGAGGGTGCATTCTGGGCGGTGTCACTGGAGAAATGGCATCTGAGCTGGA A C AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:236051418..236051638 26863196 MeRIP-seq:(Medium) rs893068043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200908,Human_RBP_ID_24553206 RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_43262 98093 RMVar_ID_98093 Human_SNP_ID_117865418 m1A Human chr2 + 236051478 236051473 236051479 TGAGCTGGACTCTGAAATAGGGGGTGATTCCCAGGGCCAGGGCCAGGGGACCAGGTGGGAAGGCG TGAGCTGGACTCTGAAATAGGGGGTGAT______GGCCAGGGCCAGGGGACCAGGTGGGAAGGCG TTCCCAG T AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:236051474..236051645 26863196 MeRIP-seq:(Medium) rs1253062858 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_8200909 RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_43262 98094 RMVar_ID_98094 Human_SNP_ID_117865423 m1A Human chr2 + 236051478 236051478 236051478 TGAGCTGGACTCTGAAATAGGGGGTGATTCCCAGGGCCAGGGCCAGGGGACCAGGTGGGAAGGCG TGAGCTGGACTCTGAAATAGGGGGTGATTCCCGGGGCCAGGGCCAGGGGACCAGGTGGGAAGGCG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:236051474..236051645 26863196 MeRIP-seq:(Medium) rs1044066048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200909 RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_43262 98095 RMVar_ID_98095 Human_SNP_ID_117886254 m1A Human chr2 - 236124169 236124169 236124169 ACGTGCTGCGACTTCTGAGCGAGAATGCGGCGAGGCTGCCGCGTCCCAGGTGCGGCGAGCAGGCG ACGTGCTGCGACTTCTGAGCGAGAATGCGGCGCGGCTGCCGCGTCCCAGGTGCGGCGAGCAGGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:236124119..236124206 26863196 MeRIP-seq:(Medium) rs1200970851 Functional Loss SNV dbSNP153 33..33 33 - - - 98096 RMVar_ID_98096 Human_SNP_ID_117898009 m1A Human chr2 - 236167685 236167685 236167685 CCTGCCCACAGGCTTCTGCTCCAGCCTGGCGCAGGGCATGGCGCTCACCTCTACGCTCATGGCCA CCTGCCCACAGGCTTCTGCTCCAGCCTGGCGCGGGGCATGGCGCTCACCTCTACGCTCATGGCCA T C GBX2 Ensembl:ENSG00000168505 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:236167679..236167864 26863196 MeRIP-seq:(Medium) rs779666496 Functional Loss SNV dbSNP153 33..33 33 - - - 98097 RMVar_ID_98097 Human_SNP_ID_117907101 m1A Human chr2 - 236203440 236203440 236203440 CCCTGCTTTCCTCTCCTGTTTCATTTCCGAGCACTCCCCATGTCAGACTCATGCCCCAGCCAACA CCCTGCTTTCCTCTCCTGTTTCATTTCCGAGCGCTCCCCATGTCAGACTCATGCCCCAGCCAACA T C ASB18 Ensembl:ENSG00000182177 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:236203389..236203514 26863196 MeRIP-seq:(Medium) rs1178591092 Functional Loss SNV dbSNP153 33..33 33 - - - 98098 RMVar_ID_98098 Human_SNP_ID_117915210 m1A Human chr2 - 236238077 236238077 236238077 GTGCGTCTCTGATTCTATCCTCTTCTCCCTACATGCCTACCTGGTACCTACCTTTAAGAGACGGC GTGCGTCTCTGATTCTATCCTCTTCTCCCTACGTGCCTACCTGGTACCTACCTTTAAGAGACGGC T C ASB18 Ensembl:ENSG00000182177 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:236237925..236238264 26863196 MeRIP-seq:(Medium) rs780892420 Functional Loss SNV dbSNP153 33..33 33 - - - 98099 RMVar_ID_98099 Human_SNP_ID_117927398 m1A Human chr2 - 236289207 236289207 236289207 ATATCCCTTTGCTCACCCACCTCCCTCCAACCAGGAAAACATTCTACCTTCCAAAATTATGCCCA ATATCCCTTTGCTCACCCACCTCCCTCCAACCGGGAAAACATTCTACCTTCCAAAATTATGCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:236289159..236289346 26863196 MeRIP-seq:(Medium) rs1361897001 Functional Loss SNV dbSNP153 33..33 33 - - - 98100 RMVar_ID_98100 Human_SNP_ID_117999991 m1A Human chr2 - 236567878 236567878 236567878 CCCTGCCCCGCACCCACCCACGGCCCGCACCCACGCCCTTCCCCGCGCCCAGACTTGTTCCGCAC CCCTGCCCCGCACCCACCCACGGCCCGCACCCCCGCCCTTCCCCGCGCCCAGACTTGTTCCGCAC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:236567829..236568000 26863196 MeRIP-seq:(Medium) rs892276677 Functional Loss SNV dbSNP153 33..33 33 - - - 98101 RMVar_ID_98101 Human_SNP_ID_118000470 m1A Human chr2 + 236569885 236569885 236569885 GGGAGCCAGCGCACAGCACAGCCAGGAAGGCGAGCGAGCCCAGCCAGCCCAGCCAGCCCAGCCAG GGGAGCCAGCGCACAGCACAGCCAGGAAGGCGCGCGAGCCCAGCCAGCCCAGCCAGCCCAGCCAG A C ACKR3 Ensembl:ENSG00000144476 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:236569797..236569900 26863196 MeRIP-seq:(Medium) rs1417373024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20437414 Human_Splice_Rec_374699 98102 RMVar_ID_98102 Human_SNP_ID_118135270 m1A Human chr2 + 237085950 237085950 237085950 TGGGGTTTGGCTGTCCGGACGGTGCAGCGGCGAGGCCGGCCGCGAAGATGCCAGTGGCGGTGATG TGGGGTTTGGCTGTCCGGACGGTGCAGCGGCGGGGCCGGCCGCGAAGATGCCAGTGGCGGTGATG A G COPS8 Ensembl:ENSG00000198612 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:237085901..237086055 26863196 MeRIP-seq:(Medium) rs529724137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546244,Human_RBP_ID_4600661,Human_RBP_ID_22076909,Human_RBP_ID_22997585 Human_Splice_Rec_374757,Human_Splice_Rec_374773,Human_Splice_Rec_374785,Human_Splice_Rec_374795,Human_Splice_Rec_374809 98103 RMVar_ID_98103 Human_SNP_ID_118135301 m1A Human chr2 + 237085987 237085987 237085987 GGCCGCGAAGATGCCAGTGGCGGTGATGGCGGAAAGCGCCTTTAGTTTCAAAAAGTTGCTGGATC GGCCGCGAAGATGCCAGTGGCGGTGATGGCGGGAAGCGCCTTTAGTTTCAAAAAGTTGCTGGATC A G COPS8 Ensembl:ENSG00000198612 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:237085910..237087495 32194978 MeRIP-seq:(Medium) rs566472436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623913,Human_RBP_ID_23859081 Human_Splice_Rec_374757,Human_Splice_Rec_374773,Human_Splice_Rec_374785,Human_Splice_Rec_374795,Human_Splice_Rec_374809 98104 RMVar_ID_98104 Human_SNP_ID_118137378 m1A Human chr2 + 237094160 237094160 237094160 GCGTATACTTCAATCATCGCCGATGATTTTGCAGCCTTTGTTGGACTTCCTGTAGAAGAGGCTGT GCGTATACTTCAATCATCGCCGATGATTTTGCGGCCTTTGTTGGACTTCCTGTAGAAGAGGCTGT A G COPS8 Ensembl:ENSG00000198612 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:237094110..237096678 32194978 MeRIP-seq:(Medium) rs1230854979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546255,Human_RBP_ID_1913083,Human_RBP_ID_9104327,Human_RBP_ID_14017820,Human_RBP_ID_19103177,Human_RBP_ID_22505301,Human_RBP_ID_23859094 Human_Splice_Rec_374766,Human_Splice_Rec_374767,Human_Splice_Rec_374793,Human_Splice_Rec_374802,Human_Splice_Rec_374803,Human_Splice_Rec_374818,Human_Splice_Rec_374819 RMVar_hsa_circ_13858,RMVar_hsa_circ_207795 98105 RMVar_ID_98105 Human_SNP_ID_118244344 m1A Human chr2 - 237517180 237517180 237517180 ATCCACCCACCACTCATCCCTCACTCCTTCATACATCTACCCAGCTGCCTACCCATCCACCCACC ATCCACCCACCACTCATCCCTCACTCCTTCATCCATCTACCCAGCTGCCTACCCATCCACCCACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:237517178..237517345 26863196 MeRIP-seq:(Medium) rs1273381998 Functional Loss SNV dbSNP153 33..33 33 - - - 98106 RMVar_ID_98106 Human_SNP_ID_118261883 m1A Human chr2 + 237574792 237574792 237574792 GAACAGGCACAGGCATCGGGGAATCAGATGGTATCAGTGGGGATAGGGCACAGCACTTTCCTGGG GAACAGGCACAGGCATCGGGGAATCAGATGGTGTCAGTGGGGATAGGGCACAGCACTTTCCTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:237574742..237574842 26863196 MeRIP-seq:(Medium) rs1287522944 Functional Loss SNV dbSNP153 33..33 33 - - - 98107 RMVar_ID_98107 Human_SNP_ID_118263155 m1A Human chr2 + 237578601 237578601 237578601 CCCATCTTGCACAGAGGCAGTCACGATTGCATAGGCTCCTCCAAGGCCTTCCTCGCCTCCTGCTA CCCATCTTGCACAGAGGCAGTCACGATTGCATGGGCTCCTCCAAGGCCTTCCTCGCCTCCTGCTA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:237578556..237578698 26863196 MeRIP-seq:(Medium) rs921132371 Functional Loss SNV dbSNP153 33..33 33 - - - 98108 RMVar_ID_98108 Human_SNP_ID_118264110 m1A Human chr2 - 237582091 237582091 237582091 GAGCAGAGGCAGAACGGACGGGAGTCCGAGGGACGGGAGTCCAAGTGAGCGCAGCCTCCCGCCCA GAGCAGAGGCAGAACGGACGGGAGTCCGAGGGGCGGGAGTCCAAGTGAGCGCAGCCTCCCGCCCA T C RAB17 Ensembl:ENSG00000124839 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:237582086..237582176 26863196 MeRIP-seq:(Medium) rs1015245619 Functional Loss SNV dbSNP153 33..33 33 - - - 98109 RMVar_ID_98109 Human_SNP_ID_118276473 m1A Human chr2 + 237627665 237627665 237627665 GCGACGCGGTCGATGGACATGGGCACCCAGGGATCGGGGCGCAAGCGGCTCCCCAACCGGGAGCG GCGACGCGGTCGATGGACATGGGCACCCAGGGGTCGGGGCGCAAGCGGCTCCCCAACCGGGAGCG A G LRRFIP1 Ensembl:ENSG00000124831 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:237627614..237683488 26863196 MeRIP-seq:(Medium) rs1347687018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243594,Human_RBP_ID_919542,Human_RBP_ID_4600692,Human_RBP_ID_17698748 Human_Splice_Rec_375719,Human_Splice_Rec_375765 98110 RMVar_ID_98110 Human_SNP_ID_118292052 m1A Human chr2 + 237692363 237692363 237692363 TCACTTAGCGGCGAGTGGCTCCGTCTCCGCGGACAGAGCGCGCGCCCCCTGGCCCGGCCCGCGAG TCACTTAGCGGCGAGTGGCTCCGTCTCCGCGGCCAGAGCGCGCGCCCCCTGGCCCGGCCCGCGAG A C LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:237692214..237692566 26863196 MeRIP-seq:(Medium) rs977286462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623914,Human_RBP_ID_9296981 RMVar_hsa_circ_207829,RMVar_hsa_circ_207830,RMVar_hsa_circ_127804 98111 RMVar_ID_98111 Human_SNP_ID_118301351 m1A Human chr2 + 237728404 237728404 237728404 GTTTTTCTGGAGAGGAAAAGGAGAATAAAACAATGCAGATGCTTGGAAGGCTCCCAGTTAAGGGG GTTTTTCTGGAGAGGAAAAGGAGAATAAAACAGTGCAGATGCTTGGAAGGCTCCCAGTTAAGGGG A G LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:237728400..237728498 26863196 MeRIP-seq:(Medium) rs558151187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64623,RMVar_hsa_circ_10372 98112 RMVar_ID_98112 Human_SNP_ID_118310659 m1A Human chr2 + 237763216 237763216 237763216 AGTACAGAAGTAGGTAGGGATCACAACGAAGAAGAGGGTGAAGAAACAGGATTAAGGGACGAGAA AGTACAGAAGTAGGTAGGGATCACAACGAAGAGGAGGGTGAAGAAACAGGATTAAGGGACGAGAA A G LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:237763039..237763491 26863196 MeRIP-seq:(Medium) rs766045695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1913135,Human_RBP_ID_2629682,Human_RBP_ID_6898169,Human_RBP_ID_22597352 RMVar_hsa_circ_6644,RMVar_hsa_circ_38724,RMVar_hsa_circ_326720,RMVar_hsa_circ_207834,RMVar_hsa_circ_24892,RMVar_hsa_circ_26674 98113 RMVar_ID_98113 Human_SNP_ID_118310823 m1A Human chr2 + 237763676 237763676 237763676 GTCCGGAGAATCCTAAAATTAAGTTGGATGGAAAACTTGACCAAGAAGGTGATGATGTACAAACA GTCCGGAGAATCCTAAAATTAAGTTGGATGGACAACTTGACCAAGAAGGTGATGATGTACAAACA A C LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:237763626..237763875 26863196 MeRIP-seq:(Medium) rs1424253788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61143,Human_RBP_ID_1913138,Human_RBP_ID_2629691,Human_RBP_ID_18756512,Human_RBP_ID_22360238 RMVar_hsa_circ_6644,RMVar_hsa_circ_38724,RMVar_hsa_circ_326720,RMVar_hsa_circ_207834,RMVar_hsa_circ_24892,RMVar_hsa_circ_26674 98114 RMVar_ID_98114 Human_SNP_ID_118333241 m1A Human chr2 - 237859729 237859729 237859729 AGGGAGCTCGGCCGGGACCCCTGGACCTACTCACCCAGGAGCAGCCAGAGGCCGCGCCGCGGGAG AGGGAGCTCGGCCGGGACCCCTGGACCTACTCGCCCAGGAGCAGCCAGAGGCCGCGCCGCGGGAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:237859653..237860001 26863410 MeRIP-seq:(Medium) rs1160011221 Functional Loss SNV dbSNP153 33..33 33 - - - 98115 RMVar_ID_98115 Human_SNP_ID_118374964 m1A Human chr2 + 238020944 238020944 238020944 GAGGAGCCCGGGTGGTGATGTGGGTGACGGCTATTCCTCAGGCTGGTGGGGACGCCCAGAGGAGG GAGGAGCCCGGGTGGTGATGTGGGTGACGGCTGTTCCTCAGGCTGGTGGGGACGCCCAGAGGAGG A G UBE2F,UBE2F-SCLY Ensembl:ENSG00000184182,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238020928..238021018 26863196 MeRIP-seq:(Medium) rs542180347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29214,RMVar_hsa_circ_47027,RMVar_hsa_circ_61399,RMVar_hsa_circ_315658 98116 RMVar_ID_98116 Human_SNP_ID_118384937 m1A Human chr2 - 238061068 238061066 238061068 CCGCGGGTGCCGGCGCATCCCTCCCCGGCGCCACGGCCGCCTCCATCCCCGCCCCACTGCTGCCG CCGCGGGTGCCGGCGCATCCCTCCCCGGCGCC__GGCCGCCTCCATCCCCGCCCCACTGCTGCCG CGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238061026..238064409 26863196 MeRIP-seq:(Medium) rs1385529219 Functional Loss DEL dbSNP153 33..34 33 - - - 98117 RMVar_ID_98117 Human_SNP_ID_118392612 m1A Human chr2 + 238092833 238092833 238092833 ACACGCCCTCCCCAGCGTGCTTTCCCTCACCCATTCCTTTCTGCCTTGGTTGCGTGCTGGCAGCC ACACGCCCTCCCCAGCGTGCTTTCCCTCACCCGTTCCTTTCTGCCTTGGTTGCGTGCTGGCAGCC A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:238092782..238092866 26863196 MeRIP-seq:(Medium) rs1386121119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17084752,Human_RBP_ID_18949954,Human_RBP_ID_20545665 RMVar_hsa_circ_73398,RMVar_hsa_circ_99518,RMVar_hsa_circ_85912,RMVar_hsa_circ_207859,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 98118 RMVar_ID_98118 Human_SNP_ID_118393816 m1A Human chr2 + 238097236 238097236 238097236 GTCAGTGCTTACTTAAACCTCATGGAAGTGGGAGCCCTGAGGGCCATGGTGTGAGCAGACTCAGG GTCAGTGCTTACTTAAACCTCATGGAAGTGGGTGCCCTGAGGGCCATGGTGTGAGCAGACTCAGG A T SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238097233..238097362 26863196 MeRIP-seq:(Medium) rs984141172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3640228 RMVar_hsa_circ_99518,RMVar_hsa_circ_207860 98119 RMVar_ID_98119 Human_SNP_ID_118393895 m1A Human chr2 + 238097477 238097477 238097477 CTGTGGGAGGTCGGAGTGGACGCAGGAGGAACACTCAGGGTTCTGGGGAGAGAGCGGAACTGTAG CTGTGGGAGGTCGGAGTGGACGCAGGAGGAACGCTCAGGGTTCTGGGGAGAGAGCGGAACTGTAG A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238097232..238097626 26863196 MeRIP-seq:(Medium) rs112677031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_829497,Human_RBP_ID_9353964,Human_RBP_ID_23859593 RMVar_hsa_circ_99518,RMVar_hsa_circ_207860 98120 RMVar_ID_98120 Human_SNP_ID_118405977 m1A Human chr2 + 238132593 238132593 238132593 GCGTGGATACTCCGTGAGGGCACCTGGGTGTCACCCACAGTGCACCTCTTCACAGGGGCCTGGGT GCGTGGATACTCCGTGAGGGCACCTGGGTGTCTCCCACAGTGCACCTCTTCACAGGGGCCTGGGT A T ESPNL Ensembl:ENSG00000144488 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238132544..238132939 26863196 MeRIP-seq:(Medium) rs986101588 Functional Loss SNV dbSNP153 33..33 33 - - - 98121 RMVar_ID_98121 Human_SNP_ID_118415816 m1A Human chr2 - 238165680 238165680 238165680 CCTCGATGCCCAAGCCTGCCGCACTCACCTGCAGGTACAGGACGCCATTCACAGAGATGGTGAAG CCTCGATGCCCAAGCCTGCCGCACTCACCTGCGGGTACAGGACGCCATTCACAGAGATGGTGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:238165595..238167164 32194978 MeRIP-seq:(Medium) rs1013114901 Functional Loss SNV dbSNP153 33..33 33 - - - 98122 RMVar_ID_98122 Human_SNP_ID_118416798 m1A Human chr2 - 238168696 238168696 238168696 GGCGTGGCCACATCACCCCCTTATCAAAACACACGGATGCAGTACCCAGGCCAGCCCAGTACTTC GGCGTGGCCACATCACCCCCTTATCAAAACACTCGGATGCAGTACCCAGGCCAGCCCAGTACTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:238168646..238168729 32194978 MeRIP-seq:(Medium) rs973621384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13810756 98123 RMVar_ID_98123 Human_SNP_ID_118422024 m1A Human chr2 - 238187845 238187845 238187845 CATCTTAGAAGCACAGGGCAGCCCCACAACAAAGAATTGTTCAGCCTGGAATGTCAGTAGTGTCG CATCTTAGAAGCACAGGGCAGCCCCACAACAAGGAATTGTTCAGCCTGGAATGTCAGTAGTGTCG T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238187842..238187941 26863196 MeRIP-seq:(Medium) rs1381478905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13811255 RMVar_hsa_circ_21048,RMVar_hsa_circ_102288,RMVar_hsa_circ_110884,RMVar_hsa_circ_104503,RMVar_hsa_circ_207874,RMVar_hsa_circ_207863,RMVar_hsa_circ_95089,RMVar_hsa_circ_207865,RMVar_hsa_circ_207864,RMVar_hsa_circ_315412,RMVar_hsa_circ_266652,RMVar_hsa_circ_354175,RMVar_hsa_circ_207862,RMVar_hsa_circ_322830,RMVar_hsa_circ_207876,RMVar_hsa_circ_85776,RMVar_hsa_circ_207875,RMVar_hsa_circ_279093,RMVar_hsa_circ_279992,RMVar_hsa_circ_276007,RMVar_hsa_circ_207878,RMVar_hsa_circ_207879,RMVar_hsa_circ_207877,RMVar_hsa_circ_39959,RMVar_hsa_circ_267586,RMVar_hsa_circ_376764,RMVar_hsa_circ_50184,RMVar_hsa_circ_207885,RMVar_hsa_circ_275468,RMVar_hsa_circ_289457,RMVar_hsa_circ_318346,RMVar_hsa_circ_207886,RMVar_hsa_circ_207884 98124 RMVar_ID_98124 Human_SNP_ID_118435450 m1A Human chr2 + 238239540 238239540 238239540 CACCCTGGACCCGCCGCACCGTCAGCTCCAGCACTTCGGCGTTCTCCAGCTTGGCCTGCACCTGC CACCCTGGACCCGCCGCACCGTCAGCTCCAGCCCTTCGGCGTTCTCCAGCTTGGCCTGCACCTGC A C AC012485.1 Ensembl:ENSG00000225057 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:238239210..238239998 26863196 MeRIP-seq:(Medium) rs1276734553 Functional Loss SNV dbSNP153 33..33 33 - - - 98125 RMVar_ID_98125 Human_SNP_ID_118435626 m1A Human chr2 - 238239905 238239905 238239905 CTAGCCCCTGCCGCGTCCCCGGCGGAGCGGGCATGGCGCCACCCGCGGCGCCTGGCCGGGACCGT CTAGCCCCTGCCGCGTCCCCGGCGGAGCGGGCTTGGCGCCACCCGCGGCGCCTGGCCGGGACCGT T A HES6 Ensembl:ENSG00000144485 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:238239800..238239974 26863196 MeRIP-seq:(Medium) rs759822505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623013,Human_RBP_ID_5471489,Human_RBP_ID_9296987,Human_RBP_ID_22450970 Human_Splice_Rec_376921,Human_Splice_Rec_376927,Human_Splice_Rec_376931,Human_Splice_Rec_376937,Human_Splice_Rec_376945,Human_Splice_Rec_376961 98126 RMVar_ID_98126 Human_SNP_ID_118435627 m1A Human chr2 - 238239905 238239905 238239905 CTAGCCCCTGCCGCGTCCCCGGCGGAGCGGGCATGGCGCCACCCGCGGCGCCTGGCCGGGACCGT CTAGCCCCTGCCGCGTCCCCGGCGGAGCGGGCGTGGCGCCACCCGCGGCGCCTGGCCGGGACCGT T C HES6 Ensembl:ENSG00000144485 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:238239800..238239974 26863196 MeRIP-seq:(Medium) rs759822505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623013,Human_RBP_ID_5471489,Human_RBP_ID_9296987,Human_RBP_ID_22450970 Human_Splice_Rec_376921,Human_Splice_Rec_376927,Human_Splice_Rec_376931,Human_Splice_Rec_376937,Human_Splice_Rec_376945,Human_Splice_Rec_376961 98127 RMVar_ID_98127 Human_SNP_ID_118435673 m1A Human chr2 - 238239972 238239972 238239972 TGGGCGGCCGCGGGGCAGCGGAGGGCGCCGGCACTCCGGTCCCCGCCGCTCCCCGTCCCCGCTGC TGGGCGGCCGCGGGGCAGCGGAGGGCGCCGGCGCTCCGGTCCCCGCCGCTCCCCGTCCCCGCTGC T C HES6 Ensembl:ENSG00000144485 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:238239876..238240025 26863410 MeRIP-seq:(Medium) rs1217731366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243778,Human_RBP_ID_777208,Human_RBP_ID_4623014,Human_RBP_ID_9330857,Human_RBP_ID_22450970,Human_RBP_ID_22997591,Human_RBP_ID_27563697 98128 RMVar_ID_98128 Human_SNP_ID_118435678 m1A Human chr2 - 238239988 238239988 238239988 ACGGCTGGGCTGCTGCTGGGCGGCCGCGGGGCAGCGGAGGGCGCCGGCACTCCGGTCCCCGCCGC ACGGCTGGGCTGCTGCTGGGCGGCCGCGGGGCGGCGGAGGGCGCCGGCACTCCGGTCCCCGCCGC T C HES6 Ensembl:ENSG00000144485 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:238239887..238240025 26863410 MeRIP-seq:(Medium) rs1217969967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243778,Human_RBP_ID_777208,Human_RBP_ID_4623014,Human_RBP_ID_9330857,Human_RBP_ID_22450970,Human_RBP_ID_22997591 98129 RMVar_ID_98129 Human_SNP_ID_118435679 m1A Human chr2 - 238239988 238239988 238239988 ACGGCTGGGCTGCTGCTGGGCGGCCGCGGGGCAGCGGAGGGCGCCGGCACTCCGGTCCCCGCCGC ACGGCTGGGCTGCTGCTGGGCGGCCGCGGGGCCGCGGAGGGCGCCGGCACTCCGGTCCCCGCCGC T G HES6 Ensembl:ENSG00000144485 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:238239887..238240025 26863410 MeRIP-seq:(Medium) rs1217969967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243778,Human_RBP_ID_777208,Human_RBP_ID_4623014,Human_RBP_ID_9330857,Human_RBP_ID_22450970,Human_RBP_ID_22997591 98130 RMVar_ID_98130 Human_SNP_ID_118449519 m1A Human chr2 - 238288640 238288640 238288640 CGGACGGGCTGACGCGGGCGCGGCCGGCGGTAAGTGGCGCGGCGCGGCCCCGCTGCGGCTTACGT CGGACGGGCTGACGCGGGCGCGGCCGGCGGTAGGTGGCGCGGCGCGGCCCCGCTGCGGCTTACGT T C PER2 Ensembl:ENSG00000132326 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:238288602..238288731 26863196 MeRIP-seq:(Medium) rs1179769612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19098993 98131 RMVar_ID_98131 Human_SNP_ID_118458175 m1A Human chr2 - 238320742 238320742 238320742 TGTCGTGCAGGTAGCGGAACGGGGGCTTGCTCAGCAGCTTCTCGGTCAGCGGCGGCCTCCGAATC TGTCGTGCAGGTAGCGGAACGGGGGCTTGCTCGGCAGCTTCTCGGTCAGCGGCGGCCTCCGAATC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:238320544..238320829 26863196 MeRIP-seq:(Medium) rs1273219455 Functional Loss SNV dbSNP153 33..33 33 - - - 98132 RMVar_ID_98132 Human_SNP_ID_118460363 m1A Human chr2 + 238329078 238329078 238329078 AATGGCGGAAACAGACACAGAGAAGGGGAGAGAGAGAGAGCCAAAGCCCGGGCCAGGCCAGACAA AATGGCGGAAACAGACACAGAGAAGGGGAGAGGGAGAGAGCCAAAGCCCGGGCCAGGCCAGACAA A G TRAF3IP1 Ensembl:ENSG00000204104 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:238329051..238329325 26863196 MeRIP-seq:(Medium) rs943687899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61796,Human_RBP_ID_24546269,Human_RBP_ID_26340486 RMVar_hsa_circ_20471,RMVar_hsa_circ_73895,RMVar_hsa_circ_44718,RMVar_hsa_circ_56492 98133 RMVar_ID_98133 Human_SNP_ID_118460374 m1A Human chr2 + 238329105 238329105 238329105 GAGAGAGAGAGAGCCAAAGCCCGGGCCAGGCCAGACAACGAGCGACAGAAAGACAGAGGCAACAG GAGAGAGAGAGAGCCAAAGCCCGGGCCAGGCCGGACAACGAGCGACAGAAAGACAGAGGCAACAG A G TRAF3IP1 Ensembl:ENSG00000204104 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:238329054..238329246 26863196 MeRIP-seq:(Medium) rs1198529589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61796 RMVar_hsa_circ_20471,RMVar_hsa_circ_73895,RMVar_hsa_circ_44718,RMVar_hsa_circ_56492 98134 RMVar_ID_98134 Human_SNP_ID_118460386 m1A Human chr2 + 238329125 238329122 238329126 CCGGGCCAGGCCAGACAACGAGCGACAGAAAGACAGAGGCAACAGGGAGCGGGACAGAGACTCCG CCGGGCCAGGCCAGACAACGAGCGACAGAA____AGAGGCAACAGGGAGCGGGACAGAGACTCCG AAGAC A TRAF3IP1 Ensembl:ENSG00000204104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:238328938..238329350;chr2:238329035..238329249;chr2:238320526..238329350;chr2:238320526..238333964 26863196 MeRIP-seq:(Medium) rs1266716435 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_61796 RMVar_hsa_circ_20471,RMVar_hsa_circ_73895,RMVar_hsa_circ_44718,RMVar_hsa_circ_56492 98135 RMVar_ID_98135 Human_SNP_ID_118460389 m1A Human chr2 + 238329125 238329125 238329125 CCGGGCCAGGCCAGACAACGAGCGACAGAAAGACAGAGGCAACAGGGAGCGGGACAGAGACTCCG CCGGGCCAGGCCAGACAACGAGCGACAGAAAGTCAGAGGCAACAGGGAGCGGGACAGAGACTCCG A T TRAF3IP1 Ensembl:ENSG00000204104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:238328938..238329350;chr2:238329035..238329249;chr2:238320526..238329350;chr2:238320526..238333964 26863196 MeRIP-seq:(Medium) rs1216950602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61796 RMVar_hsa_circ_20471,RMVar_hsa_circ_73895,RMVar_hsa_circ_44718,RMVar_hsa_circ_56492 98136 RMVar_ID_98136 Human_SNP_ID_118462592 m1A Human chr2 + 238337593 238337593 238337593 AGTAAAGGCTGCAGCGCAGCGAGGAGGGGGCCATGGCATCTGGATGAGAGGAGGTGATGGTTTGG AGTAAAGGCTGCAGCGCAGCGAGGAGGGGGCCGTGGCATCTGGATGAGAGGAGGTGATGGTTTGG A G TRAF3IP1 Ensembl:ENSG00000204104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:238337588..238337896;chr2:238337587..238337883 26863196 MeRIP-seq:(Medium) rs750830820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17138294 RMVar_hsa_circ_20471,RMVar_hsa_circ_44718,RMVar_hsa_circ_21005,RMVar_hsa_circ_56492,RMVar_hsa_circ_281515,RMVar_hsa_circ_320461 98137 RMVar_ID_98137 Human_SNP_ID_118466047 m1A Human chr2 + 238350881 238350881 238350881 TTAAACAGGGCTCGGCTGTGCCAAGCAAGTGCACCGAGAGAGAAGGGAAGGAGTAGGAGTATGTG TTAAACAGGGCTCGGCTGTGCCAAGCAAGTGCGCCGAGAGAGAAGGGAAGGAGTAGGAGTATGTG A G TRAF3IP1 Ensembl:ENSG00000204104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238350875..238351225 26863196 MeRIP-seq:(Medium) rs182590191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20471,RMVar_hsa_circ_281515,RMVar_hsa_circ_320461,RMVar_hsa_circ_349060,RMVar_hsa_circ_362096 98138 RMVar_ID_98138 Human_SNP_ID_118466210 m1A Human chr2 - 238351537 238351537 238351537 TCCTCAACACCTGCGCCCCTGTGCCTGCCGTGATCGGCAGGCCCTCTCTGTCCCGCCTTGCTCTC TCCTCAACACCTGCGCCCCTGTGCCTGCCGTGTTCGGCAGGCCCTCTCTGTCCCGCCTTGCTCTC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:238351489..238351618 26863196 MeRIP-seq:(Medium) rs994614231 Functional Loss SNV dbSNP153 33..33 33 - - - 98139 RMVar_ID_98139 Human_SNP_ID_118468701 m1A Human chr2 + 238361126 238361126 238361126 GGAGTGCAGTGGTCTGAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGCTCAAGTGATCCTCCC GGAGTGCAGTGGTCTGAATCTCGGCTCACTGCCACCTCTGCCTCCCAGGCTCAAGTGATCCTCCC A C TRAF3IP1 Ensembl:ENSG00000204104 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:238361050..238361132 26863410 MeRIP-seq:(Medium) rs986377614 Functional Loss SNV dbSNP153 33..33 33 - - - 98140 RMVar_ID_98140 Human_SNP_ID_118485027 m1A Human chr2 + 238427043 238427043 238427043 TCTGCTTCCTGCCCGAGGGGCGTGCGCGGGTCAGGGGCGGCCGCGGAGGCGGAAGCATCCATGGC TCTGCTTCCTGCCCGAGGGGCGTGCGCGGGTCTGGGGCGGCCGCGGAGGCGGAAGCATCCATGGC A T ASB1 Ensembl:ENSG00000065802 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238427005..238427187 26863196 MeRIP-seq:(Medium) rs1559410723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242187,Human_RBP_ID_4623016,Human_RBP_ID_18422054,Human_RBP_ID_26760668 Human_Splice_Rec_377133,Human_Splice_Rec_377139,Human_Splice_Rec_377145,Human_Splice_Rec_377151 RMVar_hsa_circ_128039,RMVar_hsa_circ_207904,RMVar_hsa_circ_117145,RMVar_hsa_circ_207903 98141 RMVar_ID_98141 Human_SNP_ID_118485041 m1A Human chr2 + 238427071 238427071 238427071 GGTCAGGGGCGGCCGCGGAGGCGGAAGCATCCATGGCGGAGGGCGGCAGCCCAGACGGGCGGGCA GGTCAGGGGCGGCCGCGGAGGCGGAAGCATCCGTGGCGGAGGGCGGCAGCCCAGACGGGCGGGCA A G ASB1 Ensembl:ENSG00000065802 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:238427023..238427167 26863196 MeRIP-seq:(Medium) rs1187875544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242187,Human_RBP_ID_774536,Human_RBP_ID_4623016,Human_RBP_ID_18422054,Human_RBP_ID_19098995 Human_Splice_Rec_377133,Human_Splice_Rec_377139,Human_Splice_Rec_377145,Human_Splice_Rec_377151 RMVar_hsa_circ_128039,RMVar_hsa_circ_207904,RMVar_hsa_circ_117145,RMVar_hsa_circ_207903 98142 RMVar_ID_98142 Human_SNP_ID_118486679 m1A Human chr2 - 238433505 238433505 238433505 GGCTCCTGTTAGCTCATGGAGGCCCTGCCAAGACTAACCAAAAGGGGGTGCCATCTGCAGCGAGC GGCTCCTGTTAGCTCATGGAGGCCCTGCCAAGGCTAACCAAAAGGGGGTGCCATCTGCAGCGAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238433499..238433593 26863196 MeRIP-seq:(Medium) rs1205039761 Functional Loss SNV dbSNP153 33..33 33 - - - 98143 RMVar_ID_98143 Human_SNP_ID_118489687 m1A Human chr2 - 238444635 238444635 238444635 CTGGGCCCAGCGATTCCCACTTCACTAGATTCAGGTTGGCTCCAAATTCTACCAGCAGGCTCACG CTGGGCCCAGCGATTCCCACTTCACTAGATTCCGGTTGGCTCCAAATTCTACCAGCAGGCTCACG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:238435726..238444650 32194978 MeRIP-seq:(Medium) rs1375875585 Functional Loss SNV dbSNP153 33..33 33 - - - 98144 RMVar_ID_98144 Human_SNP_ID_118490607 m1A Human chr2 + 238448178 238448178 238448178 TTCCCAAGATAGGAGAGGAACCGCAGGTGGTGAGCGGCTGGGGAGGGCCAGGACAGCCGGGGCTG TTCCCAAGATAGGAGAGGAACCGCAGGTGGTGGGCGGCTGGGGAGGGCCAGGACAGCCGGGGCTG A G ASB1 Ensembl:ENSG00000065802 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:238448129..238448320 26863196 MeRIP-seq:(Medium) rs1485932097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546577,Human_RBP_ID_827475,Human_RBP_ID_9429854 Human_miRNA_ID_498760,Human_miRNA_ID_2170999,Human_miRNA_ID_2256415,Human_miRNA_ID_2426408 RMVar_hsa_circ_207904,RMVar_hsa_circ_117145,RMVar_hsa_circ_86818,RMVar_hsa_circ_108092,RMVar_hsa_circ_207905,RMVar_hsa_circ_207907 98145 RMVar_ID_98145 Human_SNP_ID_118490741 m1A Human chr2 - 238448717 238448717 238448717 GCAGCCTGAAGGTCACACCACCACACTCACGCATGGGACTCCCACGAGGCAGCATTCCCAGGTGC GCAGCCTGAAGGTCACACCACCACACTCACGCCTGGGACTCCCACGAGGCAGCATTCCCAGGTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:238448669..238448869 32194978 MeRIP-seq:(Medium) rs1014707944 Functional Loss SNV dbSNP153 33..33 33 - - - 98146 RMVar_ID_98146 Human_SNP_ID_118594980 m1A Human chr2 + 238857099 238857096 238857099 CATCTGCTGTGCCTGGGGTCAAGGACCACTGGAGGGAGCTTGGGTTGGCCTGAGACTGTTCAGGG CATCTGCTGTGCCTGGGGTCAAGGACCACT___GGGAGCTTGGGTTGGCCTGAGACTGTTCAGGG TGGA T TWIST2 Ensembl:ENSG00000233608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238857096..238857180 26863196 MeRIP-seq:(Medium) rs917016143 Functional Loss DEL dbSNP153 31..33 33 - - - 98147 RMVar_ID_98147 Human_SNP_ID_118597801 m1A Human chr2 - 238867849 238867849 238867849 GGCCATCCGGCCATCCCCAGCCTTTGCCTCCCACTTCTCTCCCTCCCGCCTTCGAGGGATGCCCC GGCCATCCGGCCATCCCCAGCCTTTGCCTCCCGCTTCTCTCCCTCCCGCCTTCGAGGGATGCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238867843..238867924 26863196 MeRIP-seq:(Medium) rs1299067079 Functional Loss SNV dbSNP153 33..33 33 - - - 98148 RMVar_ID_98148 Human_SNP_ID_118607364 m1A Human chr2 - 238902334 238902334 238902334 ATACTCCGATTCACACAAACCCAACACCACACACCCCCACACCACACATACACATCACACACACA ATACTCCGATTCACACAAACCCAACACCACACCCCCCCACACCACACATACACATCACACACACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238902327..238902937 26863196 MeRIP-seq:(Medium) rs929353288 Functional Loss SNV dbSNP153 33..33 33 - - - 98149 RMVar_ID_98149 Human_SNP_ID_118607686 m1A Human chr2 - 238903071 238903071 238903071 ACATACCCCACAGCACACACCCCACATCACACACACTACATCACACACACATCACACACACCTCA ACATACCCCACAGCACACACCCCACATCACACGCACTACATCACACACACATCACACACACCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238903066..238903651 26863196 MeRIP-seq:(Medium) rs1227987833 Functional Loss SNV dbSNP153 33..33 33 - - - 98150 RMVar_ID_98150 Human_SNP_ID_118607759 m1A Human chr2 - 238903264 238903264 238903264 ACACACCTCACATTAGACACACCCCACATCGCACACACACTACATCTCACACACACCCATTCCAC ACACACCTCACATTAGACACACCCCACATCGCGCACACACTACATCTCACACACACCCATTCCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238903215..238903564 26863196 MeRIP-seq:(Medium) rs1398482201 Functional Loss SNV dbSNP153 33..33 33 - - - 98151 RMVar_ID_98151 Human_SNP_ID_118607934 m1A Human chr2 - 238904080 238904078 238904080 CCTCACATCACACACACACCCACATCACACACACCCCACATCACACACACCCACATCACACACAA CCTCACATCACACACACACCCACATCACACAC__CCCACATCACACACACCCACATCACACACAA GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238904077..238904445 26863196 MeRIP-seq:(Medium) rs1167114122 Functional Loss DEL dbSNP153 33..34 33 - - - 98152 RMVar_ID_98152 Human_SNP_ID_118607960 m1A Human chr2 + 238904126 238904126 238904126 GTGTGTGTGTGATGTGAGGTGTTTGTGATGTGAGGTGTGTGTGCGACGTAGTGTGTGTGATGTGG GTGTGTGTGTGATGTGAGGTGTTTGTGATGTGGGGTGTGTGTGCGACGTAGTGTGTGTGATGTGG A G TWIST2 Ensembl:ENSG00000233608 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238904068..238904201 26863196 MeRIP-seq:(Medium) rs1461141585 Functional Loss SNV dbSNP153 33..33 33 - - - 98153 RMVar_ID_98153 Human_SNP_ID_118608185 m1A Human chr2 + 238904790 238904789 238904791 TCGCAGGAATGGAAGGAAGAAAGGGAGGAAAGAAAGAAGGGAGGAAGGGGGAAGGAAGCGGAAGG TCGCAGGAATGGAAGGAAGAAAGGGAGGAAAG__AGAAGGGAGGAAGGGGGAAGGAAGCGGAAGG GAA G TWIST2 Ensembl:ENSG00000233608 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238904786..238905012 26863196 MeRIP-seq:(Medium) rs1173346178 Functional Loss DEL dbSNP153 33..34 33 - - - 98154 RMVar_ID_98154 Human_SNP_ID_118608187 m1A Human chr2 + 238904790 238904790 238904790 TCGCAGGAATGGAAGGAAGAAAGGGAGGAAAGAAAGAAGGGAGGAAGGGGGAAGGAAGCGGAAGG TCGCAGGAATGGAAGGAAGAAAGGGAGGAAAGGAAGAAGGGAGGAAGGGGGAAGGAAGCGGAAGG A G TWIST2 Ensembl:ENSG00000233608 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:238904786..238905012 26863196 MeRIP-seq:(Medium) rs912486141 Functional Loss SNV dbSNP153 33..33 33 - - - 98155 RMVar_ID_98155 Human_SNP_ID_118609549 m1A Human chr2 - 238908793 238908793 238908793 CACAAACATACCGCACACTACACACGCATCCCACTGTCCATACACACCTCATACACAAACACATA CACAAACATACCGCACACTACACACGCATCCCCCTGTCCATACACACCTCATACACAAACACATA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:238908719..238908829 26863196 MeRIP-seq:(Medium) rs1038085929 Functional Loss SNV dbSNP153 33..33 33 - - - 98156 RMVar_ID_98156 Human_SNP_ID_118609592 m1A Human chr2 - 238908910 238908910 238908910 CACACACACAAACACACCACACTGCCACATACACAAACACACTACATACACCACCACACACCACA CACACACACAAACACACCACACTGCCACATACGCAAACACACTACATACACCACCACACACCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238908904..238909156 26863196 MeRIP-seq:(Medium) rs1478623623 Functional Loss SNV dbSNP153 33..33 33 - - - 98157 RMVar_ID_98157 Human_SNP_ID_118657917 m1A Human chr2 + 239084616 239084613 239084617 CAGACAGAGACACACACACACCCCCCACAGACACACACACCACAGACAGAGACACACGTACACCC CAGACAGAGACACACACACACCCCCCACAG____ACACACCACAGACAGAGACACACGTACACCC GACAC G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:239084576..239084783 26863196 MeRIP-seq:(Medium) rs993872798 Functional Loss DEL dbSNP153 31..34 33 - - - 98158 RMVar_ID_98158 Human_SNP_ID_118657918 m1A Human chr2 + 239084616 239084613 239084617 CAGACAGAGACACACACACACCCCCCACAGACACACACACCACAGACAGAGACACACGTACACCC CAGACAGAGACACACACACACCCCCCACAGAC__ACACACCACAGACAGAGACACACGTACACCC GACAC GAC - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:239084576..239084783 26863196 MeRIP-seq:(Medium) rs993872798 Functional Loss DEL dbSNP153 33..34 33 - - - 98159 RMVar_ID_98159 Human_SNP_ID_118657928 m1A Human chr2 + 239084635 239084634 239084636 ACCCCCCACAGACACACACACCACAGACAGAGACACACGTACACCCCACACAGACACACACACCA ACCCCCCACAGACACACACACCACAGACAGAG__ACACGTACACCCCACACAGACACACACACCA GAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239084584..239084828 26863196 MeRIP-seq:(Medium) rs1189374243 Functional Loss DEL dbSNP153 33..34 33 - - - 98160 RMVar_ID_98160 Human_SNP_ID_118657951 m1A Human chr2 + 239084687 239084683 239084687 GACACACACACCACAGAGACACACCCTCCCACACAGACACACACACCATGCAACACGCCCTACAC GACACACACACCACAGAGACACACCCTCC____CAGACACACACACCATGCAACACGCCCTACAC CCACA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239084639..239084805 26863196 MeRIP-seq:(Medium) rs964999506 Functional Loss DEL dbSNP153 30..33 33 - - - 98161 RMVar_ID_98161 Human_SNP_ID_118657952 m1A Human chr2 + 239084687 239084683 239084687 GACACACACACCACAGAGACACACCCTCCCACACAGACACACACACCATGCAACACGCCCTACAC GACACACACACCACAGAGACACACCCTCCCA__CAGACACACACACCATGCAACACGCCCTACAC CCACA CCA - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239084639..239084805 26863196 MeRIP-seq:(Medium) rs964999506 Functional Loss DEL dbSNP153 32..33 33 - - - 98162 RMVar_ID_98162 Human_SNP_ID_118658680 m1A Human chr2 - 239086657 239086657 239086657 CAGAACAAGACAGAACCGCAGGGGCCCGGGAAAGGGCCTCCCTGTCACCCCTGGGAAGTCAGGCG CAGAACAAGACAGAACCGCAGGGGCCCGGGAAGGGGCCTCCCTGTCACCCCTGGGAAGTCAGGCG T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:239086467..239086726;chr2:239086324..239086839;chr2:239086329..239086717 26863196 MeRIP-seq:(Medium) rs554556347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111174,RMVar_hsa_circ_266337,RMVar_hsa_circ_110110,RMVar_hsa_circ_65307,RMVar_hsa_circ_23149,RMVar_hsa_circ_207910,RMVar_hsa_circ_92194,RMVar_hsa_circ_207911,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_264906,RMVar_hsa_circ_37514,RMVar_hsa_circ_99575,RMVar_hsa_circ_15488,RMVar_hsa_circ_269323,RMVar_hsa_circ_207917 98163 RMVar_ID_98163 Human_SNP_ID_118662700 m1A Human chr2 - 239099374 239099374 239099374 AGGGGCTTCAGCAGGCGTGGGAGTTGCTGAGCAGCCTCAAAGCATCAGCTCATCAGGCCGTGTCC AGGGGCTTCAGCAGGCGTGGGAGTTGCTGAGCTGCCTCAAAGCATCAGCTCATCAGGCCGTGTCC T A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:239099370..239099470 32194978 MeRIP-seq:(Medium) rs3791394 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12956,GWAS_ID_12957,GWAS_ID_12958,GWAS_ID_12959,GWAS_ID_12960,GWAS_ID_12961,GWAS_ID_12962,GWAS_ID_12963 RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_37514,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917 98164 RMVar_ID_98164 Human_SNP_ID_118662701 m1A Human chr2 - 239099374 239099374 239099374 AGGGGCTTCAGCAGGCGTGGGAGTTGCTGAGCAGCCTCAAAGCATCAGCTCATCAGGCCGTGTCC AGGGGCTTCAGCAGGCGTGGGAGTTGCTGAGCGGCCTCAAAGCATCAGCTCATCAGGCCGTGTCC T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:239099370..239099470 32194978 MeRIP-seq:(Medium) rs3791394 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_12956,GWAS_ID_12957,GWAS_ID_12958,GWAS_ID_12959,GWAS_ID_12960,GWAS_ID_12961,GWAS_ID_12962,GWAS_ID_12963 RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_37514,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917 98165 RMVar_ID_98165 Human_SNP_ID_118667516 m1A Human chr2 - 239115153 239115153 239115153 GGAGGCGCACGCACAGGCCGGCGTGCAGGTGAAGCAGGAGCCCATTGAGAGCGATGAGGAAGAGG GGAGGCGCACGCACAGGCCGGCGTGCAGGTGAGGCAGGAGCCCATTGAGAGCGATGAGGAAGAGG T C HDAC4 Ensembl:ENSG00000068024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239115102..239115242 26863196 MeRIP-seq:(Medium) rs1159971758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_37514,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_79524,RMVar_hsa_circ_36623,RMVar_hsa_circ_39681,RMVar_hsa_circ_74490,RMVar_hsa_circ_8016,RMVar_hsa_circ_207918 98166 RMVar_ID_98166 Human_SNP_ID_118667536 m1A Human chr2 - 239115189 239115189 239115189 GGACGAGCCCTACCTGGACCGGCTGCCGGGGCAGAAGGAGGCGCACGCACAGGCCGGCGTGCAGG GGACGAGCCCTACCTGGACCGGCTGCCGGGGCCGAAGGAGGCGCACGCACAGGCCGGCGTGCAGG T G HDAC4 Ensembl:ENSG00000068024 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239115145..239115249 26863196 MeRIP-seq:(Medium) rs766582218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_37514,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_79524,RMVar_hsa_circ_36623,RMVar_hsa_circ_39681,RMVar_hsa_circ_74490,RMVar_hsa_circ_8016,RMVar_hsa_circ_207918 98167 RMVar_ID_98167 Human_SNP_ID_118673746 m1A Human chr2 - 239134643 239134643 239134643 ACTGTGATGGTCATCGTGTGTTCTGTCCCCAGACGAGTTTGGCGCACAGACTTGTGGCACGAGAA ACTGTGATGGTCATCGTGTGTTCTGTCCCCAGTCGAGTTTGGCGCACAGACTTGTGGCACGAGAA T A HDAC4 Ensembl:ENSG00000068024 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:239134601..239134650 26863196 MeRIP-seq:(Medium) rs1026991306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2630687,Human_RBP_ID_5198074,Human_RBP_ID_22670520 Human_Splice_Rec_377226,Human_Splice_Rec_377278,Human_Splice_Rec_377354,Human_Splice_Rec_377392,Human_Splice_Rec_377422,Human_Splice_Rec_377444,Human_Splice_Rec_377452,Human_Splice_Rec_377460 RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_323302,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_47531,RMVar_hsa_circ_3330,RMVar_hsa_circ_21847 98168 RMVar_ID_98168 Human_SNP_ID_118677342 m1A Human chr2 + 239147188 239147188 239147188 AGAAGGGGGATGCTGGAGACCACCCGGGGCACATGAAGTGGCCTTCCTGGGGAGAACAGAGAAGC AGAAGGGGGATGCTGGAGACCACCCGGGGCACGTGAAGTGGCCTTCCTGGGGAGAACAGAGAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239147186..239147251 26863196 MeRIP-seq:(Medium) rs1470292148 Functional Loss SNV dbSNP153 33..33 33 - - - 98169 RMVar_ID_98169 Human_SNP_ID_118679845 m1A Human chr2 - 239155891 239155891 239155891 GCCTTCCAGAGGCTCTGCCCAGAGAATTGGTGAGGGCAGGAGCTGGAGCAGGTGCTGAGGGCGGG GCCTTCCAGAGGCTCTGCCCAGAGAATTGGTGGGGGCAGGAGCTGGAGCAGGTGCTGAGGGCGGG T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239155885..239155972 26863196 MeRIP-seq:(Medium) rs1245074195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3640258 RMVar_hsa_circ_1763,RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_86792,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_323302,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_27107,RMVar_hsa_circ_3330,RMVar_hsa_circ_266190,RMVar_hsa_circ_322203,RMVar_hsa_circ_360982,RMVar_hsa_circ_55114,RMVar_hsa_circ_207920,RMVar_hsa_circ_3810,RMVar_hsa_circ_287327 98170 RMVar_ID_98170 Human_SNP_ID_118680802 m1A Human chr2 - 239159149 239159147 239159149 TTGGGGGCGAGTAGTAGTGAGGTGCAGGTGTGAGTAGTTGGGTGAGCTGCAGGTGTGAGTGGGTG TTGGGGGCGAGTAGTAGTGAGGTGCAGGTGTG__TAGTTGGGTGAGCTGCAGGTGTGAGTGGGTG ACT A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:239159058..239159428 26863196 MeRIP-seq:(Medium) rs1225494569 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5294474,Human_RBP_ID_8200939 RMVar_hsa_circ_1763,RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_86792,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_3330,RMVar_hsa_circ_266190,RMVar_hsa_circ_322203,RMVar_hsa_circ_360982,RMVar_hsa_circ_55114,RMVar_hsa_circ_207920,RMVar_hsa_circ_3810,RMVar_hsa_circ_287327,RMVar_hsa_circ_207925,RMVar_hsa_circ_271081,RMVar_hsa_circ_311592,RMVar_hsa_circ_354135,RMVar_hsa_circ_294360,RMVar_hsa_circ_270199,RMVar_hsa_circ_207923,RMVar_hsa_circ_207924,RMVar_hsa_circ_207922 98171 RMVar_ID_98171 Human_SNP_ID_118680961 m1A Human chr2 - 239159564 239159560 239159564 GAGTGTGAGGTGTGGGAAAGGTGACAGGTGTGAGTGTGAGATGCGGGTGTGTGTGTGGGAGGTGG GAGTGTGAGGTGTGGGAAAGGTGACAGGTGTG____TGAGATGCGGGTGTGTGTGTGGGAGGTGG ACACT A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239159561..239159793 26863196 MeRIP-seq:(Medium) rs760489007 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5196227 RMVar_hsa_circ_1763,RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_86792,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_3330,RMVar_hsa_circ_266190,RMVar_hsa_circ_322203,RMVar_hsa_circ_360982,RMVar_hsa_circ_55114,RMVar_hsa_circ_207920,RMVar_hsa_circ_3810,RMVar_hsa_circ_287327,RMVar_hsa_circ_207925,RMVar_hsa_circ_271081,RMVar_hsa_circ_311592,RMVar_hsa_circ_354135,RMVar_hsa_circ_294360,RMVar_hsa_circ_270199,RMVar_hsa_circ_207923,RMVar_hsa_circ_207924,RMVar_hsa_circ_207922 98172 RMVar_ID_98172 Human_SNP_ID_118680965 m1A Human chr2 - 239159564 239159564 239159564 GAGTGTGAGGTGTGGGAAAGGTGACAGGTGTGAGTGTGAGATGCGGGTGTGTGTGTGGGAGGTGG GAGTGTGAGGTGTGGGAAAGGTGACAGGTGTGTGTGTGAGATGCGGGTGTGTGTGTGGGAGGTGG T A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239159561..239159793 26863196 MeRIP-seq:(Medium) rs1275281109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5196227 RMVar_hsa_circ_1763,RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_86792,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_3330,RMVar_hsa_circ_266190,RMVar_hsa_circ_322203,RMVar_hsa_circ_360982,RMVar_hsa_circ_55114,RMVar_hsa_circ_207920,RMVar_hsa_circ_3810,RMVar_hsa_circ_287327,RMVar_hsa_circ_207925,RMVar_hsa_circ_271081,RMVar_hsa_circ_311592,RMVar_hsa_circ_354135,RMVar_hsa_circ_294360,RMVar_hsa_circ_270199,RMVar_hsa_circ_207923,RMVar_hsa_circ_207924,RMVar_hsa_circ_207922 98173 RMVar_ID_98173 Human_SNP_ID_118681011 m1A Human chr2 - 239159711 239159711 239159711 GGGCTCCGTGGGGTGGCCAGTGTGACTGTGTGAGTGTGGAGTGTGGCCGGGGTGAGTGTGAGTGT GGGCTCCGTGGGGTGGCCAGTGTGACTGTGTGTGTGTGGAGTGTGGCCGGGGTGAGTGTGAGTGT T A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:239159602..239159801 26863196 MeRIP-seq:(Medium) rs1290526399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1763,RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_86792,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_3330,RMVar_hsa_circ_266190,RMVar_hsa_circ_322203,RMVar_hsa_circ_360982,RMVar_hsa_circ_55114,RMVar_hsa_circ_207920,RMVar_hsa_circ_3810,RMVar_hsa_circ_287327,RMVar_hsa_circ_207925,RMVar_hsa_circ_271081,RMVar_hsa_circ_311592,RMVar_hsa_circ_354135,RMVar_hsa_circ_294360,RMVar_hsa_circ_270199,RMVar_hsa_circ_207923,RMVar_hsa_circ_207924,RMVar_hsa_circ_207922 98174 RMVar_ID_98174 Human_SNP_ID_118710905 m1A Human chr2 - 239269252 239269252 239269252 GTGTGTGGGTGTGTGAATGTGTGGGTGTGTGAATGTGTGTAGATGTGTGAATGTATGTGGGTGTG GTGTGTGGGTGTGTGAATGTGTGGGTGTGTGAGTGTGTGTAGATGTGTGAATGTATGTGGGTGTG T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239269161..239269298 26863196 MeRIP-seq:(Medium) rs1317226367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5294170,Human_RBP_ID_5651742 RMVar_hsa_circ_1763,RMVar_hsa_circ_74490,RMVar_hsa_circ_3024,RMVar_hsa_circ_354135,RMVar_hsa_circ_273261,RMVar_hsa_circ_310075,RMVar_hsa_circ_271675 98175 RMVar_ID_98175 Human_SNP_ID_118710906 m1A Human chr2 + 239269255 239269253 239269255 ACCCACATACATTCACACATCTACACACATTCACACACCCACACATTCACACACCCACACACATT ACCCACATACATTCACACATCTACACACATT__CACACCCACACATTCACACACCCACACACATT TCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239269109..239269338 26863196 MeRIP-seq:(Medium) rs1472358864 Functional Loss DEL dbSNP153 32..33 33 - - - 98176 RMVar_ID_98176 Human_SNP_ID_118712746 m1A Human chr2 - 239276091 239276091 239276091 GTGAGTCAGGTCCCTGCGCAGTCCTCCCTGGCAGTGGAGGAACACTGGTTCTTTGCCTGGCCCCA GTGAGTCAGGTCCCTGCGCAGTCCTCCCTGGCGGTGGAGGAACACTGGTTCTTTGCCTGGCCCCA T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239276062..239276183 26863196 MeRIP-seq:(Medium) rs1340157622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26786668 RMVar_hsa_circ_1763,RMVar_hsa_circ_74490,RMVar_hsa_circ_3024,RMVar_hsa_circ_354135,RMVar_hsa_circ_273261,RMVar_hsa_circ_310075,RMVar_hsa_circ_271675 98177 RMVar_ID_98177 Human_SNP_ID_118714181 m1A Human chr2 - 239281027 239281027 239281027 GGTGTGTACATTGTAGAGTGGTATGTACATTGAGAGTGGTGTGTACATTGAGAGTGGTGTGTACA GGTGTGTACATTGTAGAGTGGTATGTACATTGCGAGTGGTGTGTACATTGAGAGTGGTGTGTACA T G HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239281021..239281097 26863196 MeRIP-seq:(Medium) rs1279690983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1763,RMVar_hsa_circ_74490,RMVar_hsa_circ_3024,RMVar_hsa_circ_354135,RMVar_hsa_circ_273261,RMVar_hsa_circ_310075,RMVar_hsa_circ_271675 98178 RMVar_ID_98178 Human_SNP_ID_118714267 m1A Human chr2 + 239281246 239281243 239281247 CCACTCTACACACAATGTACACACCACTCTCCACACAATGTACACACCACTCTACACACAATGAA CCACTCTACACACAATGTACACACCACTCT____ACAATGTACACACCACTCTACACACAATGAA TCCAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239281162..239281315 26863196 MeRIP-seq:(Medium) rs1344579939 Functional Loss DEL dbSNP153 31..34 33 - - - 98179 RMVar_ID_98179 Human_SNP_ID_118714498 m1A Human chr2 + 239281724 239281724 239281724 TCTACACGCAGTGTACACCCCACTCTACAATGAACACACCACTCTACACACAATGTACACGCCAC TCTACACGCAGTGTACACCCCACTCTACAATGTACACACCACTCTACACACAATGTACACGCCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239281675..239281818 26863196 MeRIP-seq:(Medium) rs1437459778 Functional Loss SNV dbSNP153 33..33 33 - - - 98180 RMVar_ID_98180 Human_SNP_ID_118716024 m1A Human chr2 + 239286545 239286544 239286545 CAGGACTGGGAAGGAAGGGAAGGAAGGGAAGGAAGGAAGACTATGGAGCAATATTTAAAGGGGCA CAGGACTGGGAAGGAAGGGAAGGAAGGGAAGG_AGGAAGACTATGGAGCAATATTTAAAGGGGCA GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239286528..239286654 26863196 MeRIP-seq:(Medium) rs11277127 Functional Loss DEL dbSNP153 33..33 33 - - - 98181 RMVar_ID_98181 Human_SNP_ID_118731015 m1A Human chr2 - 239345035 239345028 239345036 GAGGAGGGGGTGTGTAGGCAGCAGGTGCAGCCAGCTGGCAGGAGTCCAGGGGAGCTTGGACAAGG GAGGAGGGGGTGTGTAGGCAGCAGGTGCAGC________AGGAGTCCAGGGGAGCTTGGACAAGG TGCCAGCTG T HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239345031..239345113 26863196 MeRIP-seq:(Medium) rs938085126 Functional Loss DEL dbSNP153 32..39 33 - - - Human_RBP_ID_5651755,Human_RBP_ID_23283062 RMVar_hsa_circ_1763,RMVar_hsa_circ_74490,RMVar_hsa_circ_3024,RMVar_hsa_circ_354135,RMVar_hsa_circ_273261,RMVar_hsa_circ_310075,RMVar_hsa_circ_271675 98182 RMVar_ID_98182 Human_SNP_ID_118731565 m1A Human chr2 - 239346525 239346525 239346525 TGAAGGTGTGTTTGTGTGTTTTAGGGTGTGGTATGTGTTAGGGTGTGTGTGTCTTAGACTGTGTG TGAAGGTGTGTTTGTGTGTTTTAGGGTGTGGTGTGTGTTAGGGTGTGTGTGTCTTAGACTGTGTG T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:239346451..239346564 26863196 MeRIP-seq:(Medium) rs1349338343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5294197,Human_RBP_ID_17278755,Human_RBP_ID_23860656 RMVar_hsa_circ_1763,RMVar_hsa_circ_74490,RMVar_hsa_circ_3024,RMVar_hsa_circ_354135,RMVar_hsa_circ_273261,RMVar_hsa_circ_310075,RMVar_hsa_circ_271675 98183 RMVar_ID_98183 Human_SNP_ID_118731666 m1A Human chr2 + 239346720 239346719 239346721 TAAAACACACACCCTAACACACACATACCCTAACACACACGCTCTAAAACACACCCTGACACACA TAAAACACACACCCTAACACACACATACCCTA__ACACACGCTCTAAAACACACCCTGACACACA AAC A lnc-TWIST2-1,lnc-TWIST2-1:2,lnc-TWIST2-1:3 RNACentral:URS00008C3797,RNACentral:URS00008C006B,RNACentral:URS00008C3077 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:239346680..239347000 26863196 MeRIP-seq:(Medium) rs949758271 Functional Loss DEL dbSNP153 33..34 33 - - - 98184 RMVar_ID_98184 Human_SNP_ID_118731678 m1A Human chr2 + 239346746 239346745 239346747 ACCCTAACACACACGCTCTAAAACACACCCTGACACACACACCCTGTCTAAACACACACCCTAAC ACCCTAACACACACGCTCTAAAACACACCCTG__ACACACACCCTGTCTAAACACACACCCTAAC GAC G lnc-TWIST2-1,lnc-TWIST2-1:2,lnc-TWIST2-1:3 RNACentral:URS00008C3797,RNACentral:URS00008C006B,RNACentral:URS00008C3077 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:239345551..239347139 26863196 MeRIP-seq:(Medium) rs1410903626 Functional Loss DEL dbSNP153 33..34 33 - - - 98185 RMVar_ID_98185 Human_SNP_ID_118735484 m1A Human chr2 - 239360945 239360945 239360945 GAGAGAGAGGTGCCTTTCCTGTCCTTACCTGCAGCCTCTAAGCCGTCTGGAGAACTTACATTTCC GAGAGAGAGGTGCCTTTCCTGTCCTTACCTGCGGCCTCTAAGCCGTCTGGAGAACTTACATTTCC T C HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239360932..239361018 26863196 MeRIP-seq:(Medium) rs1341339580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23234247 98186 RMVar_ID_98186 Human_SNP_ID_118735524 m1A Human chr2 - 239361118 239361116 239361119 AGAGGGGCCGACAGATAATGAGAAAACAAACAACTACTTAATGTCAACATAGAATGAAATATCAG AGAGGGGCCGACAGATAATGAGAAAACAAAC___TACTTAATGTCAACATAGAATGAAATATCAG AGTT A HDAC4 Ensembl:ENSG00000068024 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239361115..239361180 26863196 MeRIP-seq:(Medium) rs1440289223 Functional Loss DEL dbSNP153 32..34 33 - - - 98187 RMVar_ID_98187 Human_SNP_ID_118746951 m1A Human chr2 - 239400381 239400381 239400381 GCCGTCTCCCGGTGCGGGGCCCGCGCCCCCCGAGCAGGTGGGCTCCGGGCCGCCGGGAGTGAGGG GCCGTCTCCCGGTGCGGGGCCCGCGCCCCCCGTGCAGGTGGGCTCCGGGCCGCCGGGAGTGAGGG T A HDAC4 Ensembl:ENSG00000068024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239400380..239400486 26863196 MeRIP-seq:(Medium) rs1457859478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22599699 Human_Splice_Rec_377209,Human_Splice_Rec_377261 98188 RMVar_ID_98188 Human_SNP_ID_118746968 m1A Human chr2 + 239400401 239400401 239400401 GAGCCCACCTGCTCGGGGGGCGCGGGCCCCGCACCGGGAGACGGCGCCGCTGCCTGCCGTGCCCA GAGCCCACCTGCTCGGGGGGCGCGGGCCCCGCCCCGGGAGACGGCGCCGCTGCCTGCCGTGCCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239400381..239400500 26863196 MeRIP-seq:(Medium) rs1279322159 Functional Loss SNV dbSNP153 33..33 33 - - - 98189 RMVar_ID_98189 Human_SNP_ID_118746987 m1A Human chr2 + 239400461 239400461 239400461 GCCCACCCCCGCGCCCCCGCCCCGGCGGGCGAAGCCGCCTCGCGGCGCGGGTGGAAAGGTCCAGA GCCCACCCCCGCGCCCCCGCCCCGGCGGGCGAGGCCGCCTCGCGGCGCGGGTGGAAAGGTCCAGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:239400376..239400475;chr2:239400426..239400475 26863196 MeRIP-seq:(Medium) rs1023211498 Functional Loss SNV dbSNP153 33..33 33 - - - 98190 RMVar_ID_98190 Human_SNP_ID_118747031 m1A Human chr2 - 239400557 239400557 239400557 CGGTCCACACCCGCCCCGCGCGCGGCCGTGGGAGGCGGGGGCCAGCGCTGGCCGCGCGCCGTGGG CGGTCCACACCCGCCCCGCGCGCGGCCGTGGGGGGCGGGGGCCAGCGCTGGCCGCGCGCCGTGGG T C HDAC4 Ensembl:ENSG00000068024 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr2:239400551..239400600 26863196 MeRIP-seq:(Medium) rs999136189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639182 98191 RMVar_ID_98191 Human_SNP_ID_118747064 m1A Human chr2 + 239400654 239400654 239400654 GCAGGCTGCGCGGGGCGCGGGGCGGGCGGCGGACAATGGCCCGCGGGCGCCGGGCCGGGGCTGCG GCAGGCTGCGCGGGGCGCGGGGCGGGCGGCGGCCAATGGCCCGCGGGCGCCGGGCCGGGGCTGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:239400618..239400768 26863196 MeRIP-seq:(Medium) rs1388138769 Functional Loss SNV dbSNP153 33..33 33 - - - 98192 RMVar_ID_98192 Human_SNP_ID_118747105 m1A Human chr2 + 239400765 239400765 239400765 CTCCGCGCCGCATCTCCTCAGCCTGCGCCGCCACCCGCCGGCGCGCGGGCTCGGGCTCGGGCGGC CTCCGCGCCGCATCTCCTCAGCCTGCGCCGCCCCCCGCCGGCGCGCGGGCTCGGGCTCGGGCGGC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:239400692..239400972 26863196 MeRIP-seq:(Medium) rs955099658 Functional Loss SNV dbSNP153 33..33 33 - - - 98193 RMVar_ID_98193 Human_SNP_ID_118747205 m1A Human chr2 - 239400947 239400947 239400947 ACGTGGGTCAATTTTTTGTGAATGAGGAGGGGAGGTTGTGGGGCCGCCGCCGCGGAGCACCGTCC ACGTGGGTCAATTTTTTGTGAATGAGGAGGGGGGGTTGTGGGGCCGCCGCCGCGGAGCACCGTCC T C HDAC4 Ensembl:ENSG00000068024 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:239400718..239400990 26863196 MeRIP-seq:(Medium) rs1350802531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639185,Human_RBP_ID_5089047,Human_RBP_ID_8110472,Human_RBP_ID_8201006,Human_RBP_ID_9330862,Human_RBP_ID_9429047,Human_RBP_ID_18193424,Human_RBP_ID_18422056,Human_RBP_ID_18462760,Human_RBP_ID_18493922,Human_RBP_ID_22417341,Human_RBP_ID_22721773,Human_RBP_ID_24376343,Human_RBP_ID_24422557,Human_RBP_ID_26786486 98194 RMVar_ID_98194 Human_SNP_ID_118747644 m1A Human chr2 + 239401789 239401789 239401789 AGGGTGTGGGGTGTAGGTCCGCCAGGCCTGCAACGGCTGCCGAGGGTCGTGGGATGCGCTCGCCG AGGGTGTGGGGTGTAGGTCCGCCAGGCCTGCACCGGCTGCCGAGGGTCGTGGGATGCGCTCGCCG A C HDAC4-AS1 Ensembl:ENSG00000222020 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239401739..239401949 26863196 MeRIP-seq:(Medium) rs775153325 Functional Loss SNV dbSNP153 33..33 33 - - - 98195 RMVar_ID_98195 Human_SNP_ID_118747645 m1A Human chr2 + 239401789 239401789 239401789 AGGGTGTGGGGTGTAGGTCCGCCAGGCCTGCAACGGCTGCCGAGGGTCGTGGGATGCGCTCGCCG AGGGTGTGGGGTGTAGGTCCGCCAGGCCTGCAGCGGCTGCCGAGGGTCGTGGGATGCGCTCGCCG A G HDAC4-AS1 Ensembl:ENSG00000222020 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239401739..239401949 26863196 MeRIP-seq:(Medium) rs775153325 Functional Loss SNV dbSNP153 33..33 33 - - - 98196 RMVar_ID_98196 Human_SNP_ID_118873769 m1A Human chr2 + 239866824 239866823 239866825 CACCAGATACACACATCACACATACCCACCACATGACACATACACTTACATACATCACACACATC CACCAGATACACACATCACACATACCCACCAC__GACACATACACTTACATACATCACACACATC CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:239866747..239866915;chr2:239866774..239866963 26863196 MeRIP-seq:(Medium) rs1343409772 Functional Loss DEL dbSNP153 33..34 33 - - - 98197 RMVar_ID_98197 Human_SNP_ID_118873964 m1A Human chr2 + 239867376 239867376 239867376 ACACACACGCCACTCATACATACTACATACCCATCACTTACACACACCACACAAACCACATACAC ACACACACGCCACTCATACATACTACATACCCGTCACTTACACACACCACACAAACCACATACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239867221..239867595 26863196 MeRIP-seq:(Medium) rs1224539916 Functional Loss SNV dbSNP153 33..33 33 - - - 98198 RMVar_ID_98198 Human_SNP_ID_118873965 m1A Human chr2 + 239867376 239867376 239867376 ACACACACGCCACTCATACATACTACATACCCATCACTTACACACACCACACAAACCACATACAC ACACACACGCCACTCATACATACTACATACCCTTCACTTACACACACCACACAAACCACATACAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239867221..239867595 26863196 MeRIP-seq:(Medium) rs1224539916 Functional Loss SNV dbSNP153 33..33 33 - - - 98199 RMVar_ID_98199 Human_SNP_ID_118880566 m1A Human chr2 - 239894198 239894159 239894199 GGAGTGAGGCTGGGATGGAGCTGAGGACAGGCAGGGAGAAGGAGTGAGGCTGGGATGGAGCTGAG GGAGTGAGGCTGGGATGGAGCTGAGGACAGG__________________________________ TCCTGTCCTCAGCTCCATCCCAGCCTCACTCCTTCTCCCTG T NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239893927..239894733 26863196 MeRIP-seq:(Medium) rs1253451641 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_207930 98200 RMVar_ID_98200 Human_SNP_ID_118880575 m1A Human chr2 - 239894198 239894198 239894198 GGAGTGAGGCTGGGATGGAGCTGAGGACAGGCAGGGAGAAGGAGTGAGGCTGGGATGGAGCTGAG GGAGTGAGGCTGGGATGGAGCTGAGGACAGGCTGGGAGAAGGAGTGAGGCTGGGATGGAGCTGAG T A NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239893927..239894733 26863196 MeRIP-seq:(Medium) rs1316065416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207930 98201 RMVar_ID_98201 Human_SNP_ID_118891299 m1A Human chr2 - 239930201 239930184 239930201 GCAGGGCTGGCTGAGGAGCAGGGGCAGTGGAGAAGCAGGGCTGGTGGAGGAGCAGGGGCGGTGGA GCAGGGCTGGCTGAGGAGCAGGGGCAGTGGAG_________________GAGCAGGGGCGGTGGA CCTCCACCAGCCCTGCTT C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239930151..239930359 26863196 MeRIP-seq:(Medium) rs1283312435 Functional Loss DEL dbSNP153 33..49 33 - - - RMVar_hsa_circ_67450 98202 RMVar_ID_98202 Human_SNP_ID_118891307 m1A Human chr2 - 239930197 239930197 239930197 GGCTGGCTGAGGAGCAGGGGCAGTGGAGAAGCAGGGCTGGTGGAGGAGCAGGGGCGGTGGAGAAG GGCTGGCTGAGGAGCAGGGGCAGTGGAGAAGCCGGGCTGGTGGAGGAGCAGGGGCGGTGGAGAAG T G NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:239930147..239930423 26863196 MeRIP-seq:(Medium) rs1360482894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67450 98203 RMVar_ID_98203 Human_SNP_ID_118891308 m1A Human chr2 - 239930201 239930201 239930201 GCAGGGCTGGCTGAGGAGCAGGGGCAGTGGAGAAGCAGGGCTGGTGGAGGAGCAGGGGCGGTGGA GCAGGGCTGGCTGAGGAGCAGGGGCAGTGGAGGAGCAGGGCTGGTGGAGGAGCAGGGGCGGTGGA T C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239930151..239930359 26863196 MeRIP-seq:(Medium) rs1359212963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67450 98204 RMVar_ID_98204 Human_SNP_ID_118903725 m1A Human chr2 - 239975713 239975713 239975713 TGGGCTGGGGGCTGGAGTGTCATGGGCTGAATAGGACCTGACAAGAAGGGGAAAGAGCAGAGAGA TGGGCTGGGGGCTGGAGTGTCATGGGCTGAATGGGACCTGACAAGAAGGGGAAAGAGCAGAGAGA T C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239975710..239975878 26863196 MeRIP-seq:(Medium) rs1227637638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8201011,Human_RBP_ID_9429449,Human_RBP_ID_17192345,Human_RBP_ID_23282888,Human_RBP_ID_26664409 RMVar_hsa_circ_67450,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931 98205 RMVar_ID_98205 Human_SNP_ID_118904794 m1A Human chr2 + 239979788 239979788 239979788 GCCACTCTCTGGCGCACCAACGCCACCACCTCACCAGGAGTACCGCTGAACTGAGGTCCCCGTGG GCCACTCTCTGGCGCACCAACGCCACCACCTCGCCAGGAGTACCGCTGAACTGAGGTCCCCGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:239979785..239980116 26863196 MeRIP-seq:(Medium) rs966174182 Functional Loss SNV dbSNP153 33..33 33 - - - 98206 RMVar_ID_98206 Human_SNP_ID_697298577 m1A Human chr22 + 11630606 11630606 11630606 AACAAAAGCCGGAGGTTCGAAGATGATCAGATACCGTCGTAGTTCCGACCATAAACGATGCCGAC AACAAAAGCCGGAGGTTCGAAGATGATCAGATGCCGTCGTAGTTCCGACCATAAACGATGCCGAC A G RF01960-012,RF01960-006,RF01960-012:2,piR-30625 RNACentral:URS00008D17FC,RNACentral:URS00006383AF,RNACentral:URS0000C3BF61,RNACentral:URS00001650DC rRNA,rRNA,rRNA,piRNA exon,intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:11630576..11630650 26863196 MeRIP-seq:(Medium) rs1353417678 Functional Loss SNV dbSNP153 33..33 33 - - - 98207 RMVar_ID_98207 Human_SNP_ID_697298581 m1A Human chr22 - 11630610 11630610 11630610 GCCAGTCGGCATCGTTTATGGTCGGAACTACGACGGTATCTGATCATCTTCGAACCTCCGGCTTT GCCAGTCGGCATCGTTTATGGTCGGAACTACGGCGGTATCTGATCATCTTCGAACCTCCGGCTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:11630576..11630650 26863196 MeRIP-seq:(Medium) rs1300699571 Functional Loss SNV dbSNP153 33..33 33 - - - 98208 RMVar_ID_98208 Human_SNP_ID_697417908 m1A Human chr22 + 12098030 12098030 12098030 GAGGGCGAAGAGGAACCCGTGGGCCTCGGGGGATCCCGGGGGGCCGGACCAGTGTCCCCTAGTTG GAGGGCGAAGAGGAACCCGTGGGCCTCGGGGGTTCCCGGGGGGCCGGACCAGTGTCCCCTAGTTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:12097980..12098124 26863196 MeRIP-seq:(Medium) rs1297609689 Functional Loss SNV dbSNP153 33..33 33 - - - 98209 RMVar_ID_98209 Human_SNP_ID_697626198 m1A Human chr22 - 12815635 12815635 12815635 GCCGGACCAGTGTTCCCTAGTTGTGGGAGCAGACGCGTGGGCGCATCGAGGGAGGGCAGGGCCTG GCCGGACCAGTGTTCCCTAGTTGTGGGAGCAGGCGCGTGGGCGCATCGAGGGAGGGCAGGGCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:12815617..12815727 26863196 MeRIP-seq:(Medium) rs1163606372 Functional Loss SNV dbSNP153 33..33 33 - - - 98210 RMVar_ID_98210 Human_SNP_ID_697846483 m1A Human chr22 + 15817494 15817494 15817494 AAGGGGGGTCCCACTGCGGGCCAGGAGGGCTCAACATCAATATATCTGAATTTCAAGCCAAGACA AAGGGGGGTCCCACTGCGGGCCAGGAGGGCTCCACATCAATATATCTGAATTTCAAGCCAAGACA A C DUXAP8 Ensembl:ENSG00000206195 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1163500550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25653093 98211 RMVar_ID_98211 Human_SNP_ID_697848257 m1A Human chr22 + 15821637 15821637 15821637 GGACGGTGTGGGCTCAGGCGCCTGGCAGGCACACGGGGCCTCTAAAGCTTGGTCACTGTCACAGA GGACGGTGTGGGCTCAGGCGCCTGGCAGGCACGCGGGGCCTCTAAAGCTTGGTCACTGTCACAGA A G DUXAP8 Ensembl:ENSG00000206195 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2844981 Functional Loss SNV dbSNP153 33..33 33 - - - 98212 RMVar_ID_98212 Human_SNP_ID_698017176 m1A Human chr22 + 16354701 16354701 16354701 ATGGAGTGGAATAGAATGGAATGGAGTGGAATAGAATGGAATGGAATGGAATGGAACGGAATGGA ATGGAGTGGAATAGAATGGAATGGAGTGGAATGGAATGGAATGGAATGGAATGGAACGGAATGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:16354661..16354762 26863196 MeRIP-seq:(Medium) rs1397220846 Functional Loss SNV dbSNP153 33..33 33 - - - 98213 RMVar_ID_98213 Human_SNP_ID_698211471 m1A Human chr22 - 17037346 17037346 17037346 GGGTTCCAGGTGGGGTTCATCCCCCTCCACTTACCGCCGAGGCCTGCCACCTCCTCCACCAACAA GGGTTCCAGGTGGGGTTCATCCCCCTCCACTTTCCGCCGAGGCCTGCCACCTCCTCCACCAACAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:17037301..17037401;chr22:17037324..17037396;chr22:17037324..17037417 26863196 MeRIP-seq:(Medium) rs551608802 Functional Loss SNV dbSNP153 33..33 33 - - - 98214 RMVar_ID_98214 Human_SNP_ID_698218668 m1A Human chr22 + 17066994 17066994 17066994 AGGAAGGGAAGGAAGGAGAGAAAGAAGGAAGGAAGGCAAGAAAGAAAAGAAAGAAAACGGGGAAG AGGAAGGGAAGGAAGGAGAGAAAGAAGGAAGGCAGGCAAGAAAGAAAAGAAAGAAAACGGGGAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17066944..17067116 26863196 MeRIP-seq:(Medium) rs1377805568 Functional Loss SNV dbSNP153 33..33 33 - - - 98215 RMVar_ID_98215 Human_SNP_ID_698218669 m1A Human chr22 + 17066994 17066994 17066994 AGGAAGGGAAGGAAGGAGAGAAAGAAGGAAGGAAGGCAAGAAAGAAAAGAAAGAAAACGGGGAAG AGGAAGGGAAGGAAGGAGAGAAAGAAGGAAGGGAGGCAAGAAAGAAAAGAAAGAAAACGGGGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17066944..17067116 26863196 MeRIP-seq:(Medium) rs1377805568 Functional Loss SNV dbSNP153 33..33 33 - - - 98216 RMVar_ID_98216 Human_SNP_ID_698227998 m1A Human chr22 - 17103709 17103705 17103709 ACCTGTGCACGCTCCCCACTCCCGTCCACACCACTCTCTCCACCTGTGCACACTCCCCACTCCCG ACCTGTGCACGCTCCCCACTCCCGTCCACACC____TCTCCACCTGTGCACACTCCCCACTCCCG AGAGT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:17103707..17103848 26863196 MeRIP-seq:(Medium) rs1459232446 Functional Loss DEL dbSNP153 33..36 33 - - - 98217 RMVar_ID_98217 Human_SNP_ID_698227999 m1A Human chr22 - 17103709 17103706 17103709 ACCTGTGCACGCTCCCCACTCCCGTCCACACCACTCTCTCCACCTGTGCACACTCCCCACTCCCG ACCTGTGCACGCTCCCCACTCCCGTCCACACC___CTCTCCACCTGTGCACACTCCCCACTCCCG GAGT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:17103707..17103848 26863196 MeRIP-seq:(Medium) rs1199087197 Functional Loss DEL dbSNP153 33..35 33 - - - 98218 RMVar_ID_98218 Human_SNP_ID_698228000 m1A Human chr22 - 17103709 17103707 17103709 ACCTGTGCACGCTCCCCACTCCCGTCCACACCACTCTCTCCACCTGTGCACACTCCCCACTCCCG ACCTGTGCACGCTCCCCACTCCCGTCCACACC__TCTCTCCACCTGTGCACACTCCCCACTCCCG AGT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:17103707..17103848 26863196 MeRIP-seq:(Medium) rs368478497 Functional Loss DEL dbSNP153 33..34 33 - - - 98219 RMVar_ID_98219 Human_SNP_ID_698228023 m1A Human chr22 - 17103750 17103746 17103750 ACCTGTGCACACTCCCCACTCCCAGACACACCACACTCTCCACCTGTGCACGCTCCCCACTCCCG ACCTGTGCACACTCCCCACTCCCAGACACACC____TCTCCACCTGTGCACGCTCCCCACTCCCG AGTGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17103742..17103877 26863196 MeRIP-seq:(Medium) rs1401945702 Functional Loss DEL dbSNP153 33..36 33 - - - 98220 RMVar_ID_98220 Human_SNP_ID_698228024 m1A Human chr22 - 17103750 17103746 17103750 ACCTGTGCACACTCCCCACTCCCAGACACACCACACTCTCCACCTGTGCACGCTCCCCACTCCCG ACCTGTGCACACTCCCCACTCCCAGACACACC__ACTCTCCACCTGTGCACGCTCCCCACTCCCG AGTGT AGT - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17103742..17103877 26863196 MeRIP-seq:(Medium) rs1401945702 Functional Loss DEL dbSNP153 33..34 33 - - - 98221 RMVar_ID_98221 Human_SNP_ID_698228025 m1A Human chr22 - 17103750 17103748 17103751 ACCTGTGCACACTCCCCACTCCCAGACACACCACACTCTCCACCTGTGCACGCTCCCCACTCCCG ACCTGTGCACACTCCCCACTCCCAGACACAC___ACTCTCCACCTGTGCACGCTCCCCACTCCCG TGTG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17103742..17103877 26863196 MeRIP-seq:(Medium) rs1459349490 Functional Loss DEL dbSNP153 32..34 33 - - - 98222 RMVar_ID_98222 Human_SNP_ID_698228029 m1A Human chr22 - 17103750 17103750 17103750 ACCTGTGCACACTCCCCACTCCCAGACACACCACACTCTCCACCTGTGCACGCTCCCCACTCCCG ACCTGTGCACACTCCCCACTCCCAGACACACCGCACTCTCCACCTGTGCACGCTCCCCACTCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17103742..17103877 26863196 MeRIP-seq:(Medium) rs1203585444 Functional Loss SNV dbSNP153 33..33 33 - - - 98223 RMVar_ID_98223 Human_SNP_ID_698228076 m1A Human chr22 + 17103851 17103851 17103851 GGTGGAGAGAGTGGTGTGGACGGGAGTGGGGAACGTGCACAGGTGGAGAGAGTGGTGTGGCTGGG GGTGGAGAGAGTGGTGTGGACGGGAGTGGGGAGCGTGCACAGGTGGAGAGAGTGGTGTGGCTGGG A G IL17RA Ensembl:ENSG00000177663 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17103561..17103933 26863196 MeRIP-seq:(Medium) rs112065328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8207090,Human_RBP_ID_22604029 RMVar_hsa_circ_30915,RMVar_hsa_circ_112989,RMVar_hsa_circ_212814,RMVar_hsa_circ_212815,RMVar_hsa_circ_80702,RMVar_hsa_circ_87282,RMVar_hsa_circ_91856,RMVar_hsa_circ_212816,RMVar_hsa_circ_212817 98224 RMVar_ID_98224 Human_SNP_ID_698228220 m1A Human chr22 - 17104291 17104291 17104291 CACACCACTCTCTCCACCTGTGCACGCTCCCCACTCCAGCCACACCACACTCTCCACCTGTGCAC CACACCACTCTCTCCACCTGTGCACGCTCCCCCCTCCAGCCACACCACACTCTCCACCTGTGCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17104249..17104318 26863196 MeRIP-seq:(Medium) rs1177346246 Functional Loss SNV dbSNP153 33..33 33 - - - 98225 RMVar_ID_98225 Human_SNP_ID_698229242 m1A Human chr22 + 17107754 17107754 17107754 TCCAGGGCCTGGAAGTGAAAAATACAGTGATGACACCAAATACACCGGTCAGTATTTCCTGGTTT TCCAGGGCCTGGAAGTGAAAAATACAGTGATGGCACCAAATACACCGGTCAGTATTTCCTGGTTT A G IL17RA Ensembl:ENSG00000177663 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17104766..17109854 32194978 MeRIP-seq:(Medium) rs150618101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2134142,Human_Splice_Rec_2134143,Human_Splice_Rec_2134166,Human_Splice_Rec_2134167 RMVar_hsa_circ_91856,RMVar_hsa_circ_212816 98226 RMVar_ID_98226 Human_SNP_ID_698230563 m1A Human chr22 - 17110929 17110929 17110929 CTACGCTTTCCCCAACCACAATCCTTCAGCTCAGGCATCTCCTCGGGGATCCCCCCTGACCTGGG CTACGCTTTCCCCAACCACAATCCTTCAGCTCCGGCATCTCCTCGGGGATCCCCCCTGACCTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17110881..17111042 26863196 MeRIP-seq:(Medium) rs988145857 Functional Loss SNV dbSNP153 33..33 33 - - - 98227 RMVar_ID_98227 Human_SNP_ID_698230581 m1A Human chr22 - 17111030 17111003 17111031 ACTGCCTCCCTCCTTCCCCTCCAGGCTCCACCAGCAGCTCCCTGACAAGCTCACTCCACTCACCT ACTGCCTCCCTCCTTCCCCTCCAGGCTCCAC____________________________TCACCT AGTGGAGTGAGCTTGTCAGGGAGCTGCTG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17110826..17111398 26863196 MeRIP-seq:(Medium) rs1339846810 Functional Loss DEL dbSNP153 32..59 33 - - - 98228 RMVar_ID_98228 Human_SNP_ID_698237655 m1A Human chr22 + 17138055 17138055 17138055 ACTCCAAAGCCCAGCCCTCCTTGCGGAAGACCAGCTGCACAGCCTCATTCACGTCATTCACCACG ACTCCAAAGCCCAGCCCTCCTTGCGGAAGACCGGCTGCACAGCCTCATTCACGTCATTCACCACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17138005..17138152 26863196 MeRIP-seq:(Medium) rs1453905110 Functional Loss SNV dbSNP153 33..33 33 - - - 98229 RMVar_ID_98229 Human_SNP_ID_698237680 m1A Human chr22 - 17138108 17138108 17138108 TTCCACGGGCACCGAGACTTATGCTTCAGTCCAGGGCTCATGGAGGCCTCCCACGTGGTGAATGA TTCCACGGGCACCGAGACTTATGCTTCAGTCCGGGGCTCATGGAGGCCTCCCACGTGGTGAATGA T C HDHD5 Ensembl:ENSG00000069998 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17138059..17138127 26863196 MeRIP-seq:(Medium) rs1381520870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_574724,Human_RBP_ID_18783814,Human_RBP_ID_23933790 Human_miRNA_ID_1981414,Human_miRNA_ID_1983138,Human_miRNA_ID_2510004,Human_miRNA_ID_2542728,Human_miRNA_ID_2544593,Human_miRNA_ID_2546431,Human_miRNA_ID_2548297,Human_miRNA_ID_2550161,Human_miRNA_ID_2552030,Human_miRNA_ID_2557443,Human_miRNA_ID_2559329,Human_miRNA_ID_2589743 RMVar_hsa_circ_109869,RMVar_hsa_circ_123389,RMVar_hsa_circ_212819,RMVar_hsa_circ_107744,RMVar_hsa_circ_212820,RMVar_hsa_circ_212818 98230 RMVar_ID_98230 Human_SNP_ID_698237741 m1A Human chr22 - 17138260 17138260 17138260 ATGATGGGGCGCCAGAACTAGGGGCCGGGGGCACACGGCAGCAACAGCCCTCAGCAAGCCAGAGC ATGATGGGGCGCCAGAACTAGGGGCCGGGGGCGCACGGCAGCAACAGCCCTCAGCAAGCCAGAGC T C HDHD5 Ensembl:ENSG00000069998 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17138220..17138313 26863196 MeRIP-seq:(Medium) rs1422617426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245623,Human_RBP_ID_574728,Human_RBP_ID_14382952,Human_RBP_ID_27491323 Human_Splice_Rec_2134208,Human_Splice_Rec_2134222,Human_Splice_Rec_2134226,Human_Splice_Rec_2134232,Human_Splice_Rec_2134238 RMVar_hsa_circ_109869,RMVar_hsa_circ_123389,RMVar_hsa_circ_212819,RMVar_hsa_circ_107744,RMVar_hsa_circ_212820,RMVar_hsa_circ_212821,RMVar_hsa_circ_212818 98231 RMVar_ID_98231 Human_SNP_ID_698240041 m1A Human chr22 + 17146615 17146615 17146615 ACGCCATCGCACACGCTCCACACCTGTGGCACACTCCTGTGAGCTTACAGGCCTTCGATCACACG ACGCCATCGCACACGCTCCACACCTGTGGCACCCTCCTGTGAGCTTACAGGCCTTCGATCACACG A C NONHSAG033192.2 RNACentral:URS00008C2B54 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17146612..17146756 26863196 MeRIP-seq:(Medium) rs1310763726 Functional Loss SNV dbSNP153 33..33 33 - - - 98232 RMVar_ID_98232 Human_SNP_ID_698240105 m1A Human chr22 + 17147007 17147007 17147007 CACCTGTGACGCCCTCCTGTGAGCTTACCGGCATTCGATCACACGCCATCGCACACGCCCCACAC CACCTGTGACGCCCTCCTGTGAGCTTACCGGCCTTCGATCACACGCCATCGCACACGCCCCACAC A C NONHSAG033192.2 RNACentral:URS00008C2B54 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17146962..17147087 26863196 MeRIP-seq:(Medium) rs174803 Functional Loss SNV dbSNP153 33..33 33 - - - 98233 RMVar_ID_98233 Human_SNP_ID_698240302 m1A Human chr22 - 17147610 17147600 17147611 GCGATGGCGTGTGATTGAAGGCCGGTAAGCTCACAGGAGGGCGCCACAGGTGTGGGGCGTGTGCG GCGATGGCGTGTGATTGAAGGCCGGTAAGCT___________GCCACAGGTGTGGGGCGTGTGCG CGCCCTCCTGTG C HDHD5 Ensembl:ENSG00000069998 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17147597..17147862 26863196 MeRIP-seq:(Medium) rs1423707807 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_5653285,Human_RBP_ID_23933833,Human_RBP_ID_27840972 RMVar_hsa_circ_70385,RMVar_hsa_circ_212821,RMVar_hsa_circ_25675,RMVar_hsa_circ_212822,RMVar_hsa_circ_287723,RMVar_hsa_circ_308343,RMVar_hsa_circ_287665,RMVar_hsa_circ_212823,RMVar_hsa_circ_212824 98234 RMVar_ID_98234 Human_SNP_ID_698240376 m1A Human chr22 + 17147776 17147776 17147776 GGCCTTCGATCACACGCCATCACACACGCCCCACACCTGTGACGCCCTCCTGTGAGCTTACCGGC GGCCTTCGATCACACGCCATCACACACGCCCCCCACCTGTGACGCCCTCCTGTGAGCTTACCGGC A C NONHSAG033192.2 RNACentral:URS00008C2B54 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17147772..17147861 26863196 MeRIP-seq:(Medium) rs912494681 Functional Loss SNV dbSNP153 33..33 33 - - - 98235 RMVar_ID_98235 Human_SNP_ID_698243507 m1A Human chr22 + 17159141 17159141 17159141 AACCCGGACGTCCTCACCTGAGCGGGGCCCACAGCATAGCACCTGCGGGCGGGGCGGCCCTGGAG AACCCGGACGTCCTCACCTGAGCGGGGCCCACTGCATAGCACCTGCGGGCGGGGCGGCCCTGGAG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:17159126..17159250 26863410 MeRIP-seq:(Medium) rs1479088859 Functional Loss SNV dbSNP153 33..33 33 - - - 98236 RMVar_ID_98236 Human_SNP_ID_698364640 m1A Human chr22 + 17598265 17598265 17598265 TCAACATCGTTTTTGGTGGCAATTTTGTACATAGGAATTGCCTTCTGCACTGCAGCCTGGAAGTA TCAACATCGTTTTTGGTGGCAATTTTGTACATGGGAATTGCCTTCTGCACTGCAGCCTGGAAGTA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:17598216..17600687 32194978 MeRIP-seq:(Medium) rs28396972 Functional Loss SNV dbSNP153 33..33 33 - - - 98237 RMVar_ID_98237 Human_SNP_ID_698373124 m1A Human chr22 + 17628687 17628687 17628687 CGGTGAACAGTAGGCTCGAGTTTAGGTTTGAAAGGTGAGGTGAGAGAAATCGGCAAAGGGAACCC CGGTGAACAGTAGGCTCGAGTTTAGGTTTGAACGGTGAGGTGAGAGAAATCGGCAAAGGGAACCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:17628615..17628750;chr22:17628613..17628750 26863196 MeRIP-seq:(Medium) rs1347209923 Functional Loss SNV dbSNP153 33..33 33 - - - 98238 RMVar_ID_98238 Human_SNP_ID_698373125 m1A Human chr22 + 17628687 17628687 17628687 CGGTGAACAGTAGGCTCGAGTTTAGGTTTGAAAGGTGAGGTGAGAGAAATCGGCAAAGGGAACCC CGGTGAACAGTAGGCTCGAGTTTAGGTTTGAAGGGTGAGGTGAGAGAAATCGGCAAAGGGAACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr22:17628615..17628750;chr22:17628613..17628750 26863196 MeRIP-seq:(Medium) rs1347209923 Functional Loss SNV dbSNP153 33..33 33 - - - 98239 RMVar_ID_98239 Human_SNP_ID_698373131 m1A Human chr22 + 17628697 17628697 17628697 TAGGCTCGAGTTTAGGTTTGAAAGGTGAGGTGAGAGAAATCGGCAAAGGGAACCCCTGCGCAGAT TAGGCTCGAGTTTAGGTTTGAAAGGTGAGGTGGGAGAAATCGGCAAAGGGAACCCCTGCGCAGAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17628626..17628750 26863196 MeRIP-seq:(Medium) rs1239544195 Functional Loss SNV dbSNP153 33..33 33 - - - 98240 RMVar_ID_98240 Human_SNP_ID_698373174 m1A Human chr22 - 17628749 17628749 17628749 CAGTCACCTGGCAGGAACCGGAACCCGCGGTTATAAAGTAAAGGAACCCGAGATCTGCGCAGGGG CAGTCACCTGGCAGGAACCGGAACCCGCGGTTCTAAAGTAAAGGAACCCGAGATCTGCGCAGGGG T G ATP6V1E1 Ensembl:ENSG00000131100 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:17628655..17628766 26863410 MeRIP-seq:(Medium) rs1350554402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23934213,Human_RBP_ID_27031030 98241 RMVar_ID_98241 Human_SNP_ID_698376109 m1A Human chr22 - 17638806 17638806 17638806 GTTGCTTCCGACAGGGTCCCCCAGCGGCGGTGAGTGCTCCGACCCGCGGCCCTAATCTACCGCCG GTTGCTTCCGACAGGGTCCCCCAGCGGCGGTGGGTGCTCCGACCCGCGGCCCTAATCTACCGCCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:17638762..17638908 26863196 MeRIP-seq:(Medium) rs1057437444 Functional Loss SNV dbSNP153 33..33 33 - - - 98242 RMVar_ID_98242 Human_SNP_ID_698400469 m1A Human chr22 + 17726917 17726917 17726917 CACTAGGCCCTGAGTCCTGGCAGCAGATTGCAATGGATCCTGAAGAAGTGAAAAGCTTAGACAGC CACTAGGCCCTGAGTCCTGGCAGCAGATTGCAGTGGATCCTGAAGAAGTGAAAAGCTTAGACAGC A G BCL2L13 Ensembl:ENSG00000099968 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:17726725..17726925 32194978 MeRIP-seq:(Medium) rs1310765125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782149 RMVar_hsa_circ_212847 98243 RMVar_ID_98243 Human_SNP_ID_698400661 m1A Human chr22 + 17727430 17727430 17727430 CTAGACTGTCCCCCGCCGGTGAGATGAAGCCCATGCCGCTGTCTGAGGGCAAGTCTATACTGCTG CTAGACTGTCCCCCGCCGGTGAGATGAAGCCCGTGCCGCTGTCTGAGGGCAAGTCTATACTGCTG A G BCL2L13 Ensembl:ENSG00000099968 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17727181..17727600 26863196 MeRIP-seq:(Medium) rs1388721797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9124243 Human_miRNA_ID_1062151 98244 RMVar_ID_98244 Human_SNP_ID_698400814 m1A Human chr22 - 17727952 17727952 17727952 AACCCTCTCTCGCTAAAGCAGTGGGTCTCAATAGGGGATGTTCACACGGGACATTTGGCAATGTC AACCCTCTCTCGCTAAAGCAGTGGGTCTCAATGGGGGATGTTCACACGGGACATTTGGCAATGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:17727901..17728169 32194978 MeRIP-seq:(Medium) rs908510624 Functional Loss SNV dbSNP153 33..33 33 - - - 98245 RMVar_ID_98245 Human_SNP_ID_698403560 m1A Human chr22 + 17738189 17738188 17738189 TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGCAGCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGC_GCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17738087..17738273 26863196 MeRIP-seq:(Medium) rs1569037222 Functional Loss DEL dbSNP153 33..33 33 - - - 98246 RMVar_ID_98246 Human_SNP_ID_698403561 m1A Human chr22 + 17738189 17738189 17738189 TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGCAGCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGCCGCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17738087..17738273 26863196 MeRIP-seq:(Medium) rs895511972 Functional Loss SNV dbSNP153 33..33 33 - - - 98247 RMVar_ID_98247 Human_SNP_ID_698403562 m1A Human chr22 + 17738189 17738189 17738189 TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGCAGCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG TCTCCTTCTCCATGTCTCTAGGGTAGGCCTGCGGCAGCTGCTCCAGGGCAGTGGCCAGGTCCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17738087..17738273 26863196 MeRIP-seq:(Medium) rs895511972 Functional Loss SNV dbSNP153 33..33 33 - - - 98248 RMVar_ID_98248 Human_SNP_ID_698403907 m1A Human chr22 + 17739415 17739415 17739415 GCCAGGCCGTTCACCAGGCCCGGAGGGATGCTACGGTCCATGCTGTCCCCGACCTGGGCGAGGTG GCCAGGCCGTTCACCAGGCCCGGAGGGATGCTGCGGTCCATGCTGTCCCCGACCTGGGCGAGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17739317..17739486 26863196 MeRIP-seq:(Medium) rs768249904 Functional Loss SNV dbSNP153 33..33 33 - - - 98249 RMVar_ID_98249 Human_SNP_ID_698406927 m1A Human chr22 - 17750154 17750154 17750154 GTCCCTTTCCAGGTCGCCACTGGGACACTGTGAACCAGGAGTGAGTCGGAGCTGCCGCGCTGCCC GTCCCTTTCCAGGTCGCCACTGGGACACTGTGGACCAGGAGTGAGTCGGAGCTGCCGCGCTGCCC T C BID Ensembl:ENSG00000015475 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17750101..17750227 26863196 MeRIP-seq:(Medium) rs756181395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1607578,Human_RBP_ID_1939480,Human_RBP_ID_4708012,Human_RBP_ID_8943141,Human_RBP_ID_22674893 Human_Splice_Rec_2134894,Human_Splice_Rec_2134895,Human_Splice_Rec_2134910,Human_Splice_Rec_2134911,Human_Splice_Rec_2134920,Human_Splice_Rec_2134921,Human_Splice_Rec_2134936,Human_Splice_Rec_2134937,Human_Splice_Rec_2134956,Human_Splice_Rec_2134957,Human_Splice_Rec_2134968,Human_Splice_Rec_2134969,Human_Splice_Rec_2134978,Human_Splice_Rec_2134979,Human_Splice_Rec_2135004,Human_Splice_Rec_2135005 RMVar_hsa_circ_15082 98250 RMVar_ID_98250 Human_SNP_ID_698414242 m1A Human chr22 - 17774386 17774386 17774386 CGGCCCGGACGCGCCCGCGCCCCCGCGGCTGGAGGGTGGTGAGTGCACCCGCGCCCCTCCCGGGG CGGCCCGGACGCGCCCGCGCCCCCGCGGCTGGGGGGTGGTGAGTGCACCCGCGCCCCTCCCGGGG T C BID Ensembl:ENSG00000015475 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr22:17774376..17774450;chr22:17774376..17774475 32194978 MeRIP-seq:(Medium) rs1472802704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684115,Human_RBP_ID_9300469,Human_RBP_ID_9333105 Human_Splice_Rec_2134909,Human_Splice_Rec_2134919,Human_Splice_Rec_2134927,Human_Splice_Rec_2134935,Human_Splice_Rec_2134945,Human_Splice_Rec_2134955,Human_Splice_Rec_2134967,Human_Splice_Rec_2134993,Human_Splice_Rec_2135003 98251 RMVar_ID_98251 Human_SNP_ID_698414278 m1A Human chr22 + 17774445 17774445 17774445 GGGCCGAGGCAGCGTCTCCCAGGCGCGCGGACACGGTCGACTACCCGCTTCCTCCTTATGGCGCC GGGCCGAGGCAGCGTCTCCCAGGCGCGCGGACCCGGTCGACTACCCGCTTCCTCCTTATGGCGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17774302..17774500 26863196 MeRIP-seq:(Medium) rs1274589401 Functional Loss SNV dbSNP153 33..33 33 - - - 98252 RMVar_ID_98252 Human_SNP_ID_698414279 m1A Human chr22 + 17774445 17774445 17774445 GGGCCGAGGCAGCGTCTCCCAGGCGCGCGGACACGGTCGACTACCCGCTTCCTCCTTATGGCGCC GGGCCGAGGCAGCGTCTCCCAGGCGCGCGGACGCGGTCGACTACCCGCTTCCTCCTTATGGCGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17774302..17774500 26863196 MeRIP-seq:(Medium) rs1274589401 Functional Loss SNV dbSNP153 33..33 33 - - - 98253 RMVar_ID_98253 Human_SNP_ID_698418302 m1A Human chr22 + 17788842 17788842 17788842 TCAAGTTGAAGCACAGTGTGGTTCCCATGGAAAGCCCAAGGTCAGCACAGCCACTCAGCCTGCTC TCAAGTTGAAGCACAGTGTGGTTCCCATGGAAGGCCCAAGGTCAGCACAGCCACTCAGCCTGCTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17788795..17788896 32194978 MeRIP-seq:(Medium) rs936993395 Functional Loss SNV dbSNP153 33..33 33 - - - 98254 RMVar_ID_98254 Human_SNP_ID_698418303 m1A Human chr22 + 17788842 17788842 17788842 TCAAGTTGAAGCACAGTGTGGTTCCCATGGAAAGCCCAAGGTCAGCACAGCCACTCAGCCTGCTC TCAAGTTGAAGCACAGTGTGGTTCCCATGGAATGCCCAAGGTCAGCACAGCCACTCAGCCTGCTC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17788795..17788896 32194978 MeRIP-seq:(Medium) rs936993395 Functional Loss SNV dbSNP153 33..33 33 - - - 98255 RMVar_ID_98255 Human_SNP_ID_698418727 m1A Human chr22 + 17790240 17790196 17790240 GTCTCCTGTGATGCTGGGGTGGGCATGACTGGACGCCCCCATCCTGGGTCTCGATCGCACCCTGA _________________________________CGCCCCCATCCTGGGTCTCGATCGCACCCTGA CCGCACCTCCATGTCTCCTGTGATGCTGGGGTGGGCATGACTGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:17790196..17790267;chr22:17790190..17790285 26863196 MeRIP-seq:(Medium) rs1238853822 Functional Loss DEL dbSNP153 1..33 33 - - - 98256 RMVar_ID_98256 Human_SNP_ID_698418948 m1A Human chr22 - 17790838 17790837 17790839 CAATGAGATGCTGGAGGTGGTGGAGCAGAGAGACTCACTGGTGGCGCTGCTGGAGGAGCAGCGGC CAATGAGATGCTGGAGGTGGTGGAGCAGAGA__CTCACTGGTGGCGCTGCTGGAGGAGCAGCGGC GTC G AC016026.1,MICAL3 Ensembl:ENSG00000093100,Ensembl:ENSG00000243156 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17790787..17790906 26863196 MeRIP-seq:(Medium) rs754293433 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_930446,Human_RBP_ID_1136719,Human_RBP_ID_4684186,Human_RBP_ID_5529729,Human_RBP_ID_7093577,Human_RBP_ID_26345643 Human_Splice_Rec_2135072,Human_Splice_Rec_2135134,Human_Splice_Rec_2135138,Human_Splice_Rec_2135148,Human_Splice_Rec_2135426 98257 RMVar_ID_98257 Human_SNP_ID_698418954 m1A Human chr22 - 17790868 17790868 17790868 GGAGGAGCTGTCAGAAGAGAAGCAGATTCTCAATGAGATGCTGGAGGTGGTGGAGCAGAGAGACT GGAGGAGCTGTCAGAAGAGAAGCAGATTCTCAGTGAGATGCTGGAGGTGGTGGAGCAGAGAGACT T C AC016026.1,MICAL3 Ensembl:ENSG00000093100,Ensembl:ENSG00000243156 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17790817..17791068 26863196 MeRIP-seq:(Medium) rs774634742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930446,Human_RBP_ID_5101236,Human_RBP_ID_5599746,Human_RBP_ID_7093577 Human_Splice_Rec_2135072,Human_Splice_Rec_2135134,Human_Splice_Rec_2135138,Human_Splice_Rec_2135148,Human_Splice_Rec_2135426 98258 RMVar_ID_98258 Human_SNP_ID_698418955 m1A Human chr22 - 17790875 17790875 17790875 AGACTGAGGAGGAGCTGTCAGAAGAGAAGCAGATTCTCAATGAGATGCTGGAGGTGGTGGAGCAG AGACTGAGGAGGAGCTGTCAGAAGAGAAGCAGGTTCTCAATGAGATGCTGGAGGTGGTGGAGCAG T C AC016026.1,MICAL3 Ensembl:ENSG00000093100,Ensembl:ENSG00000243156 lincRNA,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17790825..17810753 26863196 MeRIP-seq:(Medium) rs183092756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930446,Human_RBP_ID_4684188,Human_RBP_ID_5101236,Human_RBP_ID_5599208,Human_RBP_ID_22265608 Human_Splice_Rec_2135072,Human_Splice_Rec_2135134,Human_Splice_Rec_2135138,Human_Splice_Rec_2135148,Human_Splice_Rec_2135426 98259 RMVar_ID_98259 Human_SNP_ID_698426604 m1A Human chr22 - 17817602 17817602 17817602 CGTCGGACTCAGGGGGCCCAGATGGCTCTTTCACTTCATCCGAGGGCTCCAGTGGGAAGAGCAAG CGTCGGACTCAGGGGGCCCAGATGGCTCTTTCGCTTCATCCGAGGGCTCCAGTGGGAAGAGCAAG T C MICAL3 Ensembl:ENSG00000243156 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17817496..17818146 32194978 MeRIP-seq:(Medium) rs779315183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930449 RMVar_hsa_circ_56451,RMVar_hsa_circ_354000,RMVar_hsa_circ_352769 98260 RMVar_ID_98260 Human_SNP_ID_698426977 m1A Human chr22 + 17818292 17818292 17818292 CTCGCCCGGGGGTGGCGGTGGGGGCGGGCTGGAGGGGGGCGTGAGCATGGCGGAGTCCGAGGTGT CTCGCCCGGGGGTGGCGGTGGGGGCGGGCTGGGGGGGGGCGTGAGCATGGCGGAGTCCGAGGTGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17818245..17818396 32194978 MeRIP-seq:(Medium) rs867208173 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98261 RMVar_ID_98261 Human_SNP_ID_698427338 m1A Human chr22 + 17819058 17819058 17819058 GCATCAGCTTTGGGCTTCTCTTTGGGGAGCAAAGGCTCAGGGAAAAGGCGCTCCTCAGGTGATTT GCATCAGCTTTGGGCTTCTCTTTGGGGAGCAACGGCTCAGGGAAAAGGCGCTCCTCAGGTGATTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17819009..17819127 26863196 MeRIP-seq:(Medium) rs374948398 Functional Loss SNV dbSNP153 33..33 33 - - - 98262 RMVar_ID_98262 Human_SNP_ID_698427339 m1A Human chr22 + 17819058 17819058 17819058 GCATCAGCTTTGGGCTTCTCTTTGGGGAGCAAAGGCTCAGGGAAAAGGCGCTCCTCAGGTGATTT GCATCAGCTTTGGGCTTCTCTTTGGGGAGCAAGGGCTCAGGGAAAAGGCGCTCCTCAGGTGATTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17819009..17819127 26863196 MeRIP-seq:(Medium) rs374948398 Functional Loss SNV dbSNP153 33..33 33 - - - 98263 RMVar_ID_98263 Human_SNP_ID_698428404 m1A Human chr22 + 17822109 17822109 17822109 GACACCCTCAGCTCCAGCTCTGCTTCCCCCTCAGCTGGGCACGGCAAACGCAGCTCTCTGTCAGC GACACCCTCAGCTCCAGCTCTGCTTCCCCCTCGGCTGGGCACGGCAAACGCAGCTCTCTGTCAGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17822060..17823036 32194978 MeRIP-seq:(Medium) rs1427535590 Functional Loss SNV dbSNP153 33..33 33 - - - 98264 RMVar_ID_98264 Human_SNP_ID_698429496 m1A Human chr22 - 17826007 17826007 17826007 GGTTTATGGGAGGATGATGGTGGAGAGGGAAGAGCAGAGGATGGGCGGGTGCTATTCAGCAGAAA GGTTTATGGGAGGATGATGGTGGAGAGGGAAGTGCAGAGGATGGGCGGGTGCTATTCAGCAGAAA T A MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17826005..17826117 26863196 MeRIP-seq:(Medium) rs1017570491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3675767,Human_RBP_ID_21985679,Human_RBP_ID_22480116 RMVar_hsa_circ_354454 98265 RMVar_ID_98265 Human_SNP_ID_698444207 m1A Human chr22 - 17877060 17877057 17877061 CCATAACCTCCATAACTTCCCTAACCTCCATAACCTCCCTAACCTCCATAACCTCCCTAACCTCC CCATAACCTCCATAACTTCCCTAACCTCCAT____TCCCTAACCTCCATAACCTCCCTAACCTCC AGGTT A MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17877025..17877126 26863196 MeRIP-seq:(Medium) rs1423871432 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_9124293,Human_RBP_ID_21937695,Human_RBP_ID_25653901 RMVar_hsa_circ_21360,RMVar_hsa_circ_212853,RMVar_hsa_circ_58884,RMVar_hsa_circ_322005,RMVar_hsa_circ_58996,RMVar_hsa_circ_340563,RMVar_hsa_circ_270960,RMVar_hsa_circ_212854,RMVar_hsa_circ_312006,RMVar_hsa_circ_300193,RMVar_hsa_circ_75375,RMVar_hsa_circ_291139,RMVar_hsa_circ_64594,RMVar_hsa_circ_73057,RMVar_hsa_circ_212856,RMVar_hsa_circ_212858,RMVar_hsa_circ_212859,RMVar_hsa_circ_212857,RMVar_hsa_circ_40443,RMVar_hsa_circ_315752,RMVar_hsa_circ_37867,RMVar_hsa_circ_48972,RMVar_hsa_circ_212861 98266 RMVar_ID_98266 Human_SNP_ID_698447117 m1A Human chr22 - 17886028 17886028 17886028 ATTGACCAGGAGGAAGCTCCTCGGGGCCACAGAGGAGAAAGACCGACCCTGGTGAGCACTCTGAC ATTGACCAGGAGGAAGCTCCTCGGGGCCACAGGGGAGAAAGACCGACCCTGGTGAGCACTCTGAC T C MICAL3 Ensembl:ENSG00000243156 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17885977..17887335 32194978 MeRIP-seq:(Medium) rs762210038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14386263 Human_Splice_Rec_2135038,Human_Splice_Rec_2135102,Human_Splice_Rec_2135222,Human_Splice_Rec_2135260,Human_Splice_Rec_2135296,Human_Splice_Rec_2135334,Human_Splice_Rec_2135354,Human_Splice_Rec_2135390 RMVar_hsa_circ_21360,RMVar_hsa_circ_212853,RMVar_hsa_circ_58884,RMVar_hsa_circ_322005,RMVar_hsa_circ_58996,RMVar_hsa_circ_340563,RMVar_hsa_circ_270960,RMVar_hsa_circ_212854,RMVar_hsa_circ_312006,RMVar_hsa_circ_300193,RMVar_hsa_circ_75375,RMVar_hsa_circ_291139,RMVar_hsa_circ_64594,RMVar_hsa_circ_16429,RMVar_hsa_circ_73057,RMVar_hsa_circ_212856,RMVar_hsa_circ_212858,RMVar_hsa_circ_212859,RMVar_hsa_circ_212857,RMVar_hsa_circ_40443,RMVar_hsa_circ_315752,RMVar_hsa_circ_29673,RMVar_hsa_circ_37867,RMVar_hsa_circ_48972,RMVar_hsa_circ_212861,RMVar_hsa_circ_281827,RMVar_hsa_circ_299676,RMVar_hsa_circ_339444,RMVar_hsa_circ_347407,RMVar_hsa_circ_312964,RMVar_hsa_circ_299244,RMVar_hsa_circ_73161,RMVar_hsa_circ_212862,RMVar_hsa_circ_212864,RMVar_hsa_circ_212865,RMVar_hsa_circ_212863 98267 RMVar_ID_98267 Human_SNP_ID_698448941 m1A Human chr22 + 17892785 17892785 17892785 CTGCTGGTCCTCACATCCACCCTGGCATCCCAATGGCACGTCAAATTCACAATGTCCAAATGACT CTGCTGGTCCTCACATCCACCCTGGCATCCCAGTGGCACGTCAAATTCACAATGTCCAAATGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17892781..17892972 26863196 MeRIP-seq:(Medium) rs930952594 Functional Loss SNV dbSNP153 33..33 33 - - - 98268 RMVar_ID_98268 Human_SNP_ID_698449040 m1A Human chr22 - 17893170 17893170 17893170 GATCTGGGCCTGATGCTGGGGATGAAGAAGGGAGGAGGCAGTGGAGGAGACCTCAGACTTTGGGC GATCTGGGCCTGATGCTGGGGATGAAGAAGGGGGGAGGCAGTGGAGGAGACCTCAGACTTTGGGC T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17893168..17893264 26863196 MeRIP-seq:(Medium) rs1239036766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834051 RMVar_hsa_circ_58884,RMVar_hsa_circ_322005,RMVar_hsa_circ_58996,RMVar_hsa_circ_270960,RMVar_hsa_circ_212854,RMVar_hsa_circ_300193,RMVar_hsa_circ_75375,RMVar_hsa_circ_64594,RMVar_hsa_circ_16429,RMVar_hsa_circ_212856,RMVar_hsa_circ_212857,RMVar_hsa_circ_339444,RMVar_hsa_circ_312964,RMVar_hsa_circ_299244,RMVar_hsa_circ_73161,RMVar_hsa_circ_44607,RMVar_hsa_circ_212864,RMVar_hsa_circ_212865,RMVar_hsa_circ_269150,RMVar_hsa_circ_334211,RMVar_hsa_circ_23941,RMVar_hsa_circ_46086,RMVar_hsa_circ_110660,RMVar_hsa_circ_300115,RMVar_hsa_circ_212866,RMVar_hsa_circ_212867,RMVar_hsa_circ_107666,RMVar_hsa_circ_212868 98269 RMVar_ID_98269 Human_SNP_ID_698455464 m1A Human chr22 - 17917331 17917331 17917331 TGTCCGGGTAGCTGGCGGTGTTGTTTACCAAGATGCAGAACACTAGGGAAGGAACAGGCTCTGGC TGTCCGGGTAGCTGGCGGTGTTGTTTACCAAGGTGCAGAACACTAGGGAAGGAACAGGCTCTGGC T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17917329..17917790 26863196 MeRIP-seq:(Medium) rs1040963477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 98270 RMVar_ID_98270 Human_SNP_ID_698455804 m1A Human chr22 - 17918676 17918676 17918676 AGCAGGGATGGAGAGGCTGGCGGCAGGAAAGGAGGCAACAGAGGGAAGGCGTGTGTATGGGTGCA AGCAGGGATGGAGAGGCTGGCGGCAGGAAAGGCGGCAACAGAGGGAAGGCGTGTGTATGGGTGCA T G MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17918625..17918757 26863196 MeRIP-seq:(Medium) rs909871247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 98271 RMVar_ID_98271 Human_SNP_ID_698468198 m1A Human chr22 + 17966108 17966108 17966108 TGCAGGATCTGCCATCTGCTGCCAGCTTCATCATTCTCAGACAGAACCCTCATCCTGCCACATCC TGCAGGATCTGCCATCTGCTGCCAGCTTCATCGTTCTCAGACAGAACCCTCATCCTGCCACATCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17966103..17966340 26863196 MeRIP-seq:(Medium) rs565114885 Functional Loss SNV dbSNP153 33..33 33 - - - 98272 RMVar_ID_98272 Human_SNP_ID_698472485 m1A Human chr22 + 17980736 17980734 17980736 ACTCCAGCCACACCCACTTTCTCCAGAGTGCCACAGTTTCCGTCTTATCATTCCGCCCGTCTTAT ACTCCAGCCACACCCACTTTCTCCAGAGTGC__CAGTTTCCGTCTTATCATTCCGCCCGTCTTAT CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17980734..17980934 26863196 MeRIP-seq:(Medium) rs755969657 Functional Loss DEL dbSNP153 32..33 33 - - - 98273 RMVar_ID_98273 Human_SNP_ID_698473216 m1A Human chr22 + 17983072 17983072 17983072 ATGGGTCTCTTCTAGCTCAGCAGGTCTCTCTCATTCTGTCTACTGTTTTTTCTTTTTTTAGAGAA ATGGGTCTCTTCTAGCTCAGCAGGTCTCTCTCCTTCTGTCTACTGTTTTTTCTTTTTTTAGAGAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17983067..17983315 26863196 MeRIP-seq:(Medium) rs1471696591 Functional Loss SNV dbSNP153 33..33 33 - - - 98274 RMVar_ID_98274 Human_SNP_ID_698473280 m1A Human chr22 + 17983271 17983271 17983271 CTTGGGTCTTCACCCCTCCCCATTTCCCTGGGACCCTCCCTGCACCCCCCTAGGCTGGCTTTGGC CTTGGGTCTTCACCCCTCCCCATTTCCCTGGGCCCCTCCCTGCACCCCCCTAGGCTGGCTTTGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17983251..17983495 26863196 MeRIP-seq:(Medium) rs1156705062 Functional Loss SNV dbSNP153 33..33 33 - - - 98275 RMVar_ID_98275 Human_SNP_ID_698473361 m1A Human chr22 + 17983591 17983560 17983592 ACTCTGTACTCCCAAGTACAAGGCTGAAGCTAAATCTGCCTCCTCAGAGTCTCCACATGGCTTAC AC________________________________TCTGCCTCCTCAGAGTCTCCACATGGCTTAC CTCTGTACTCCCAAGTACAAGGCTGAAGCTAAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17983589..17983757 26863196 MeRIP-seq:(Medium) rs1349731950 Functional Loss DEL dbSNP153 3..34 33 - - - 98276 RMVar_ID_98276 Human_SNP_ID_698473384 m1A Human chr22 + 17983652 17983652 17983652 TTACCTCCCTAGAAGGCAGTGCTGCTTGTCCCACACCAGGTCTTCTGGTCCACGCCTCTTCTCCG TTACCTCCCTAGAAGGCAGTGCTGCTTGTCCCCCACCAGGTCTTCTGGTCCACGCCTCTTCTCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17983647..17983761 26863196 MeRIP-seq:(Medium) rs927756431 Functional Loss SNV dbSNP153 33..33 33 - - - 98277 RMVar_ID_98277 Human_SNP_ID_698483977 m1A Human chr22 - 18024372 18024372 18024372 GGATCGCAGCTGCAGGGGTTGTGCGAGCAGCCACGGCGGCACCTGTGCCCTGCGGGCACCCACCC GGATCGCAGCTGCAGGGGTTGTGCGAGCAGCCGCGGCGGCACCTGTGCCCTGCGGGCACCCACCC T C MICAL3 Ensembl:ENSG00000243156 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:18024324..18024496 26863196 MeRIP-seq:(Medium) rs1349969222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684322 Human_Splice_Rec_2135009,Human_Splice_Rec_2135073 RMVar_hsa_circ_212874,RMVar_hsa_circ_103449 98278 RMVar_ID_98278 Human_SNP_ID_698484012 m1A Human chr22 - 18024500 18024500 18024500 AGTCCCGGCGGGGAGCGCCCGCGTAGGCAGGCACCCGGGGCAGCCCTCCGTCCTCGCCGCGCGGC AGTCCCGGCGGGGAGCGCCCGCGTAGGCAGGCGCCCGGGGCAGCCCTCCGTCCTCGCCGCGCGGC T C MICAL3 Ensembl:ENSG00000243156 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:18024267..18024521 26863196 MeRIP-seq:(Medium) rs139544925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212874,RMVar_hsa_circ_103449 98279 RMVar_ID_98279 Human_SNP_ID_698498849 m1A Human chr22 + 18078387 18078387 18078387 GGGCCTTGGACCCGGACTCGTTATGAAGAGCGATTCTTCGACCTCTGCAGCCCCCCTCAGGGGGC GGGCCTTGGACCCGGACTCGTTATGAAGAGCGGTTCTTCGACCTCTGCAGCCCCCCTCAGGGGGC A G PEX26 Ensembl:ENSG00000215193 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:18078034..18078391 32194978 MeRIP-seq:(Medium) rs1464374837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_574991,Human_RBP_ID_4684347,Human_RBP_ID_22086170,Human_RBP_ID_22265694 Human_Splice_Rec_2135436,Human_Splice_Rec_2135444 98280 RMVar_ID_98280 Human_SNP_ID_698498949 m1A Human chr22 - 18078528 18078528 18078528 AGGCCCGCTCGCAGGTCTCCAGCGCCGCCCGGAAGTCCAGGTGCACCACCAGGAGGTCGGCCGCC AGGCCCGCTCGCAGGTCTCCAGCGCCGCCCGGTAGTCCAGGTGCACCACCAGGAGGTCGGCCGCC T A AC016027.1 Ensembl:ENSG00000225335 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:18078483..18078631 32194978 MeRIP-seq:(Medium) rs758213085 Functional Loss SNV dbSNP153 33..33 33 - - - 98281 RMVar_ID_98281 Human_SNP_ID_698499364 m1A Human chr22 - 18080016 18080016 18080016 GAACCGATCTGATGAGTCAGCAAAGAAGACTTACCACAGCTCCAGGACTTTGGGGGGTAGCTTTT GAACCGATCTGATGAGTCAGCAAAGAAGACTTGCCACAGCTCCAGGACTTTGGGGGGTAGCTTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:18079982..18080064 26863196 MeRIP-seq:(Medium) rs758806142 Functional Loss SNV dbSNP153 33..33 33 - - - 98282 RMVar_ID_98282 Human_SNP_ID_698502250 m1A Human chr22 + 18090426 18090426 18090426 TCGCTCCCCTTGGCCTCTGTGCCTTGGCTCGCACTGTTCCTACTGAAGGCCTAGCACCTGCTCTT TCGCTCCCCTTGGCCTCTGTGCCTTGGCTCGCGCTGTTCCTACTGAAGGCCTAGCACCTGCTCTT A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:18090376..18090475 26863196 MeRIP-seq:(Medium) rs1249759239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575017,Human_RBP_ID_14388314,Human_RBP_ID_27491466 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 98283 RMVar_ID_98283 Human_SNP_ID_698502367 m1A Human chr22 - 18090869 18090869 18090869 AGCCCCTTCCTAGAGGCGAACCCTCCGCCCCCACCCCCAGGCACTATCTGTCCTGCTTGCACCCA AGCCCCTTCCTAGAGGCGAACCCTCCGCCCCCCCCCCCAGGCACTATCTGTCCTGCTTGCACCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:18090821..18090915 26863196 MeRIP-seq:(Medium) rs1256694334 Functional Loss SNV dbSNP153 33..33 33 - - - 98284 RMVar_ID_98284 Human_SNP_ID_698502553 m1A Human chr22 + 18091570 18091570 18091570 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAAGGGTTGCAGTGAGCTGAGATCGCGCCATTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGAGGGTTGCAGTGAGCTGAGATCGCGCCATTGC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs768456070 Functional Loss SNV dbSNP153 33..33 33 - - - 98285 RMVar_ID_98285 Human_SNP_ID_698520318 m1A Human chr22 - 18157641 18157640 18157641 CCTTGCTCATTCGTGATCACTCCAAAACCCCCAGGCCGCAGCTGCCTGGCCCGCGTTCAGGACAG CCTTGCTCATTCGTGATCACTCCAAAACCCCC_GGCCGCAGCTGCCTGGCCCGCGTTCAGGACAG CT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:18157558..18157687 26863196 MeRIP-seq:(Medium) rs1222950282 Functional Loss DEL dbSNP153 33..33 33 - - - 98286 RMVar_ID_98286 Human_SNP_ID_698522957 m1A Human chr22 - 18168068 18168067 18168068 GTTATAACAACAGAAAATGGACTAACACATACAGGGGCAGCAAATACCAAGAGAATCCCCTTACC GTTATAACAACAGAAAATGGACTAACACATAC_GGGGCAGCAAATACCAAGAGAATCCCCTTACC CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:18168018..18169925 32194978 MeRIP-seq:(Medium) rs1190299349 Functional Loss DEL dbSNP153 33..33 33 - - - 98287 RMVar_ID_98287 Human_SNP_ID_698630058 m1A Human chr22 + 18906348 18906348 18906348 GGATGACGTGAGCTGGGGGCGCTCGTCGCTGCAGCCGGCGGCTAGCGGGCGTCCGCGCCATGGAG GGATGACGTGAGCTGGGGGCGCTCGTCGCTGCCGCCGGCGGCTAGCGGGCGTCCGCGCCATGGAG A C AC007326.4,DGCR6 Ensembl:ENSG00000283809,Ensembl:ENSG00000183628 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:18906286..18906568 26863196 MeRIP-seq:(Medium) rs990580076 Functional Loss SNV dbSNP153 33..33 33 - - - 98288 RMVar_ID_98288 Human_SNP_ID_698630075 m1A Human chr22 + 18906375 18906375 18906375 GCTGCAGCCGGCGGCTAGCGGGCGTCCGCGCCATGGAGCGCTACGCGGGCGCCTTGGAGGAGGTG GCTGCAGCCGGCGGCTAGCGGGCGTCCGCGCCGTGGAGCGCTACGCGGGCGCCTTGGAGGAGGTG A G AC007326.4,DGCR6 Ensembl:ENSG00000283809,Ensembl:ENSG00000183628 Protein coding,Protein coding start codon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:18906325..18906527 26863196 MeRIP-seq:(Medium) rs754926861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684487 Human_Splice_Rec_2136043 98289 RMVar_ID_98289 Human_SNP_ID_698630076 m1A Human chr22 - 18906376 18906376 18906376 CCACCTCCTCCAAGGCGCCCGCGTAGCGCTCCATGGCGCGGACGCCCGCTAGCCGCCGGCTGCAG CCACCTCCTCCAAGGCGCCCGCGTAGCGCTCCGTGGCGCGGACGCCCGCTAGCCGCCGGCTGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:18906326..18906597 26863196 MeRIP-seq:(Medium) rs1412264091 Functional Loss SNV dbSNP153 33..33 33 - - - 98290 RMVar_ID_98290 Human_SNP_ID_698630077 m1A Human chr22 + 18906379 18906379 18906379 CAGCCGGCGGCTAGCGGGCGTCCGCGCCATGGAGCGCTACGCGGGCGCCTTGGAGGAGGTGGCGG CAGCCGGCGGCTAGCGGGCGTCCGCGCCATGGGGCGCTACGCGGGCGCCTTGGAGGAGGTGGCGG A G AC007326.4,DGCR6 Ensembl:ENSG00000283809,Ensembl:ENSG00000183628 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:18906329..18906473 26863196 MeRIP-seq:(Medium) rs1289575469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684487 Human_Splice_Rec_2136043 98291 RMVar_ID_98291 Human_SNP_ID_698635683 m1A Human chr22 - 18930986 18930986 18930986 CCCGAGGAGGCAGAGCACAAGGAGATGGAGTAAGGCCTGCCCGGTGTCTGCGGGCTTTCTGATCA CCCGAGGAGGCAGAGCACAAGGAGATGGAGTAGGGCCTGCCCGGTGTCTGCGGGCTTTCTGATCA T C PRODH Ensembl:ENSG00000100033 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:18930981..18931048 26863196 MeRIP-seq:(Medium) rs1435500940 Functional Loss SNV dbSNP153 33..33 33 - - - 98292 RMVar_ID_98292 Human_SNP_ID_698646081 m1A Human chr22 - 18970761 18970761 18970761 TGGCCCTCCCGGCCGCCCGGCTACGCTTCCCCAGCCTTGGAAGCCCTGGACGGGCCCTGCGGCTC TGGCCCTCCCGGCCGCCCGGCTACGCTTCCCCGGCCTTGGAAGCCCTGGACGGGCCCTGCGGCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:18970750..18971014 26863196 MeRIP-seq:(Medium) rs902301139 Functional Loss SNV dbSNP153 33..33 33 - - - 98293 RMVar_ID_98293 Human_SNP_ID_698646685 m1A Human chr22 + 18972771 18972771 18972771 GGATTTGGGTCCTGGCTCAGCCACCTGCTGGCAGTGTGACCTTGGGTGTGACAGGTCACCTCTCT GGATTTGGGTCCTGGCTCAGCCACCTGCTGGCGGTGTGACCTTGGGTGTGACAGGTCACCTCTCT A G DGCR9,DGCR5 Ensembl:ENSG00000273032,Ensembl:ENSG00000237517 lincRNA,Pseudogene intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:18972769..18972888 32194978 MeRIP-seq:(Medium) rs566295109 Functional Loss SNV dbSNP153 33..33 33 - - - 98294 RMVar_ID_98294 Human_SNP_ID_698646686 m1A Human chr22 + 18972771 18972771 18972771 GGATTTGGGTCCTGGCTCAGCCACCTGCTGGCAGTGTGACCTTGGGTGTGACAGGTCACCTCTCT GGATTTGGGTCCTGGCTCAGCCACCTGCTGGCTGTGTGACCTTGGGTGTGACAGGTCACCTCTCT A T DGCR9,DGCR5 Ensembl:ENSG00000273032,Ensembl:ENSG00000237517 lincRNA,Pseudogene intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:18972769..18972888 32194978 MeRIP-seq:(Medium) rs566295109 Functional Loss SNV dbSNP153 33..33 33 - - - 98295 RMVar_ID_98295 Human_SNP_ID_698663225 m1A Human chr22 - 19036825 19036825 19036825 GGCCGGTCAGACACGTAGGGGGCAGTGAGGAAACGGGGTAAAGTGGACCATGCAGGCTGCAGAGG GGCCGGTCAGACACGTAGGGGGCAGTGAGGAATCGGGGTAAAGTGGACCATGCAGGCTGCAGAGG T A DGCR2 Ensembl:ENSG00000070413 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19036718..19036996 26863196 MeRIP-seq:(Medium) rs1476392781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_265308,Human_RBP_ID_1068856,Human_RBP_ID_5119980,Human_RBP_ID_9354246,Human_RBP_ID_26500549,Human_RBP_ID_27304058 98296 RMVar_ID_98296 Human_SNP_ID_698687770 m1A Human chr22 + 19122365 19122363 19122365 GAAAGAGCTTCGGCTGGGCCGCGGGCTGGCGCACACTCTCGGCTGCAACCTCAGGCACCGACTCC GAAAGAGCTTCGGCTGGGCCGCGGGCTGGCG__CACTCTCGGCTGCAACCTCAGGCACCGACTCC GCA G AC004471.1 Ensembl:ENSG00000223461 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19122204..19122425 26863196 MeRIP-seq:(Medium) rs1355334471 Functional Loss DEL dbSNP153 32..33 33 - - - 98297 RMVar_ID_98297 Human_SNP_ID_698687774 m1A Human chr22 - 19122371 19122371 19122371 GCAGCTGGAGTCGGTGCCTGAGGTTGCAGCCGAGAGTGTGCGCCAGCCCGCGGCCCAGCCGAAGC GCAGCTGGAGTCGGTGCCTGAGGTTGCAGCCGGGAGTGTGCGCCAGCCCGCGGCCCAGCCGAAGC T C DGCR2 Ensembl:ENSG00000070413 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19122253..19122400 26863196 MeRIP-seq:(Medium) rs952339354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708034,Human_RBP_ID_5473402,Human_RBP_ID_9332539,Human_RBP_ID_18423609,Human_RBP_ID_18496989 98298 RMVar_ID_98298 Human_SNP_ID_698691120 m1A Human chr22 + 19134291 19134291 19134291 CGGGTCCTGTGTGAGAGGGGTGCGTGTGGCAGAGCCAGGCGCCGGTGTGCTTGTGGGGGTCTGCA CGGGTCCTGTGTGAGAGGGGTGCGTGTGGCAGGGCCAGGCGCCGGTGTGCTTGTGGGGGTCTGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19134240..19134334 26863196 MeRIP-seq:(Medium) rs975182762 Functional Loss SNV dbSNP153 33..33 33 - - - 98299 RMVar_ID_98299 Human_SNP_ID_698692465 m1A Human chr22 + 19138765 19138765 19138765 CATCAGAGAGTATCTACTCGTCTTGCTCCCAGACTCAGAAAGCCTCTGCTCTCTGCCAACCCAGG CATCAGAGAGTATCTACTCGTCTTGCTCCCAGGCTCAGAAAGCCTCTGCTCTCTGCCAACCCAGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19138719..19138874 26863196 MeRIP-seq:(Medium) rs1016106547 Functional Loss SNV dbSNP153 33..33 33 - - - 98300 RMVar_ID_98300 Human_SNP_ID_698692590 m1A Human chr22 - 19139212 19139212 19139212 ATAAGAACACGCGCTTCCTTAGGGACCCCTTCAGCCAAGCCCTGAGCAGGTGCCAGCTCCAGCAG ATAAGAACACGCGCTTCCTTAGGGACCCCTTCGGCCAAGCCCTGAGCAGGTGCCAGCTCCAGCAG T C ESS2 Ensembl:ENSG00000100056 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19139130..19139226 26863196 MeRIP-seq:(Medium) rs1233531282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1028338,Human_RBP_ID_3962679,Human_RBP_ID_18445122,Human_RBP_ID_26822172 Human_Splice_Rec_2136456,Human_Splice_Rec_2136457,Human_Splice_Rec_2136474,Human_Splice_Rec_2136475,Human_Splice_Rec_2136492,Human_Splice_Rec_2136493 RMVar_hsa_circ_61616 98301 RMVar_ID_98301 Human_SNP_ID_698693724 m1A Human chr22 + 19142747 19142747 19142747 GGTCCTCATACAGGGTGGCGGGGGCTCCCGGGACATCTTGCCCAAGGCAGAGCCAAACTTGATGG GGTCCTCATACAGGGTGGCGGGGGCTCCCGGGTCATCTTGCCCAAGGCAGAGCCAAACTTGATGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19140023..19144138 32194978 MeRIP-seq:(Medium) rs201700740 Functional Loss SNV dbSNP153 33..33 33 - - - 98302 RMVar_ID_98302 Human_SNP_ID_698694368 m1A Human chr22 + 19144613 19144613 19144613 CGGGGGCCTGGACGCGGCGGGAAGCAACAAGGACGACGCTGATGCGCCCGGCGTCTCCATCGCTA CGGGGGCCTGGACGCGGCGGGAAGCAACAAGGGCGACGCTGATGCGCCCGGCGTCTCCATCGCTA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:19144515..19144628;chr22:19144435..19144650;chr22:19144458..19144628 26863196 MeRIP-seq:(Medium) rs1316988424 Functional Loss SNV dbSNP153 33..33 33 - - - 98303 RMVar_ID_98303 Human_SNP_ID_698694371 m1A Human chr22 + 19144616 19144616 19144616 GGGCCTGGACGCGGCGGGAAGCAACAAGGACGACGCTGATGCGCCCGGCGTCTCCATCGCTATCC GGGCCTGGACGCGGCGGGAAGCAACAAGGACGGCGCTGATGCGCCCGGCGTCTCCATCGCTATCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19144485..19144650 26863196 MeRIP-seq:(Medium) rs145246090 Functional Loss SNV dbSNP153 33..33 33 - - - 98304 RMVar_ID_98304 Human_SNP_ID_698694372 m1A Human chr22 + 19144616 19144616 19144616 GGGCCTGGACGCGGCGGGAAGCAACAAGGACGACGCTGATGCGCCCGGCGTCTCCATCGCTATCC GGGCCTGGACGCGGCGGGAAGCAACAAGGACGTCGCTGATGCGCCCGGCGTCTCCATCGCTATCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19144485..19144650 26863196 MeRIP-seq:(Medium) rs145246090 Functional Loss SNV dbSNP153 33..33 33 - - - 98305 RMVar_ID_98305 Human_SNP_ID_698694377 m1A Human chr22 - 19144620 19144620 19144620 CCTGGGATAGCGATGGAGACGCCGGGCGCATCAGCGTCGTCCTTGTTGCTTCCCGCCGCGTCCAG CCTGGGATAGCGATGGAGACGCCGGGCGCATCTGCGTCGTCCTTGTTGCTTCCCGCCGCGTCCAG T A ESS2 Ensembl:ENSG00000100056 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19144184..19144634 26863196 MeRIP-seq:(Medium) rs751020265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684817,Human_RBP_ID_17989102,Human_RBP_ID_22086187,Human_RBP_ID_22819396,Human_RBP_ID_26344977 98306 RMVar_ID_98306 Human_SNP_ID_698694378 m1A Human chr22 - 19144620 19144620 19144620 CCTGGGATAGCGATGGAGACGCCGGGCGCATCAGCGTCGTCCTTGTTGCTTCCCGCCGCGTCCAG CCTGGGATAGCGATGGAGACGCCGGGCGCATCCGCGTCGTCCTTGTTGCTTCCCGCCGCGTCCAG T G ESS2 Ensembl:ENSG00000100056 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19144184..19144634 26863196 MeRIP-seq:(Medium) rs751020265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684817,Human_RBP_ID_17989102,Human_RBP_ID_22086187,Human_RBP_ID_22819396,Human_RBP_ID_26344977 98307 RMVar_ID_98307 Human_SNP_ID_698703168 m1A Human chr22 + 19172294 19172294 19172294 CAGAACTTGGGGGCAGAGGGATGAGATGGTGCATCCCTTGAGGTCACTTCAGGAGATGACACTCC CAGAACTTGGGGGCAGAGGGATGAGATGGTGCCTCCCTTGAGGTCACTTCAGGAGATGACACTCC A C LINC01311 Ensembl:ENSG00000260924 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19172034..19172554 26863196 MeRIP-seq:(Medium) rs368770886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1614281,Human_RBP_ID_3675774,Human_RBP_ID_4709384,Human_RBP_ID_5205806,Human_RBP_ID_5324492,Human_RBP_ID_5601528,Human_RBP_ID_8209057,Human_RBP_ID_9333116 98308 RMVar_ID_98308 Human_SNP_ID_698703996 m1A Human chr22 + 19175626 19175626 19175626 GGTTTATTCTGCCTTGGCAGGGTGGTCCTGAGAGTGGTGGGTGCCACCCTGTCCGGGGCGGAGAG GGTTTATTCTGCCTTGGCAGGGTGGTCCTGAGGGTGGTGGGTGCCACCCTGTCCGGGGCGGAGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19175601..19175625 26863196 MeRIP-seq:(Medium) rs1555922028 Functional Loss SNV dbSNP153 33..33 33 - - - 98309 RMVar_ID_98309 Human_SNP_ID_698704047 m1A Human chr22 - 19175787 19175787 19175787 GGTCCTCGGCCCTGTAGCCCTGGCCCGGTCCCAGTCCGGTGCCTTCCACCCTGCCCTGGCCTACC GGTCCTCGGCCCTGTAGCCCTGGCCCGGTCCCGGTCCGGTGCCTTCCACCCTGCCCTGGCCTACC T C SLC25A1 Ensembl:ENSG00000100075 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:19175688..19175812 26863410 MeRIP-seq:(Medium) rs1409442032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575173,Human_RBP_ID_1101272,Human_RBP_ID_5119656,Human_RBP_ID_8545464,Human_RBP_ID_17660399,Human_RBP_ID_23934967 Human_miRNA_ID_1964983,Human_miRNA_ID_2764437,Human_miRNA_ID_2933207 RMVar_hsa_circ_84259,RMVar_hsa_circ_115252,RMVar_hsa_circ_126172,RMVar_hsa_circ_97585,RMVar_hsa_circ_212910,RMVar_hsa_circ_212911,RMVar_hsa_circ_212912,RMVar_hsa_circ_212909 98310 RMVar_ID_98310 Human_SNP_ID_698704565 m1A Human chr22 - 19176935 19176935 19176935 TGCCTGCCTTCCCGCAGGGCTGAAGGGGACGTACCAGGGCCTCACAGCCACTGTCCTGAAGCAGG TGCCTGCCTTCCCGCAGGGCTGAAGGGGACGTGCCAGGGCCTCACAGCCACTGTCCTGAAGCAGG T C SLC25A1 Ensembl:ENSG00000100075 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19176827..19176958 26863196 MeRIP-seq:(Medium) rs1555922517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929686,Human_RBP_ID_4709755,Human_RBP_ID_22674917,Human_RBP_ID_27304169 Human_Splice_Rec_2136516,Human_Splice_Rec_2136517,Human_Splice_Rec_2136532,Human_Splice_Rec_2136533,Human_Splice_Rec_2136546,Human_Splice_Rec_2136547,Human_Splice_Rec_2136560,Human_Splice_Rec_2136561 Human_miRNA_ID_2673589 RMVar_hsa_circ_115252,RMVar_hsa_circ_126172,RMVar_hsa_circ_101917,RMVar_hsa_circ_212910,RMVar_hsa_circ_212909,RMVar_hsa_circ_74502,RMVar_hsa_circ_212914,RMVar_hsa_circ_95973,RMVar_hsa_circ_212913 98311 RMVar_ID_98311 Human_SNP_ID_698705139 m1A Human chr22 - 19178180 19178180 19178180 CATCACCTTCCCCACCGAGTACGTGAAGACGCAGCTGCAGCTGGACGAGCGCTCGCACCCGCCGC CATCACCTTCCCCACCGAGTACGTGAAGACGCTGCTGCAGCTGGACGAGCGCTCGCACCCGCCGC T A SLC25A1 Ensembl:ENSG00000100075 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19177609..19178450 26863196 MeRIP-seq:(Medium) rs1555923296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575204,Human_RBP_ID_4708375,Human_RBP_ID_23015550 Human_Splice_Rec_2136508,Human_Splice_Rec_2136509,Human_Splice_Rec_2136524,Human_Splice_Rec_2136525,Human_Splice_Rec_2136540,Human_Splice_Rec_2136541,Human_Splice_Rec_2136553,Human_Splice_Rec_2136564 Human_miRNA_ID_2014247,Human_miRNA_ID_2760646 RMVar_hsa_circ_115252,RMVar_hsa_circ_101917,RMVar_hsa_circ_212909,RMVar_hsa_circ_212914 98312 RMVar_ID_98312 Human_SNP_ID_698705151 m1A Human chr22 - 19178219 19178219 19178219 GGTCCCTGCAGGCGGCCTGGCGGGTGGCATCGAGATCTGCATCACCTTCCCCACCGAGTACGTGA GGTCCCTGCAGGCGGCCTGGCGGGTGGCATCGGGATCTGCATCACCTTCCCCACCGAGTACGTGA T C SLC25A1 Ensembl:ENSG00000100075 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:19177874..19178345;chr22:19177652..19178400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_246522,Human_RBP_ID_575204,Human_RBP_ID_782183,Human_RBP_ID_1607691,Human_RBP_ID_3961923,Human_RBP_ID_4684878,Human_RBP_ID_9341304,Human_RBP_ID_17982118,Human_RBP_ID_18193947,Human_RBP_ID_19111542 Human_Splice_Rec_2136508,Human_Splice_Rec_2136509,Human_Splice_Rec_2136524,Human_Splice_Rec_2136525,Human_Splice_Rec_2136540,Human_Splice_Rec_2136541,Human_Splice_Rec_2136553,Human_Splice_Rec_2136564 RMVar_hsa_circ_115252,RMVar_hsa_circ_101917,RMVar_hsa_circ_212909,RMVar_hsa_circ_212914 98313 RMVar_ID_98313 Human_SNP_ID_698705294 m1A Human chr22 + 19178551 19178551 19178551 AGCGTCCCGGGCCCACCCAGAAGCGCGGCGGGAGAGGGGTCCGCGTCCCGGAGGGGCCCACCTGC AGCGTCCCGGGCCCACCCAGAAGCGCGGCGGGGGAGGGGTCCGCGTCCCGGAGGGGCCCACCTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19178547..19178775 26863196 MeRIP-seq:(Medium) rs1555923545 Functional Loss SNV dbSNP153 33..33 33 - - - 98314 RMVar_ID_98314 Human_SNP_ID_698705311 m1A Human chr22 + 19178585 19178585 19178585 AGGGGTCCGCGTCCCGGAGGGGCCCACCTGCCAGGATCGCCTTCCCCGGGTGCGTCAGCTTGGCC AGGGGTCCGCGTCCCGGAGGGGCCCACCTGCCTGGATCGCCTTCCCCGGGTGCGTCAGCTTGGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19178576..19178725 32194978 MeRIP-seq:(Medium) rs1555923570 Functional Loss SNV dbSNP153 33..33 33 - - - 98315 RMVar_ID_98315 Human_SNP_ID_698705355 m1A Human chr22 + 19178684 19178673 19178684 GCGGGGCGCGGGGCGCGGGCATGGCGGGCGGGAGGCGGGGCGCCCTGTGGCGGCTTCGGGTCCGA GCGGGGCGCGGGGCGCGGGCAT___________GGCGGGGCGCCCTGTGGCGGCTTCGGGTCCGA TGGCGGGCGGGA T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr22:19178576..19178775 26863410 MeRIP-seq:(Medium) rs1555923634 Functional Loss DEL dbSNP153 23..33 33 - - - 98316 RMVar_ID_98316 Human_SNP_ID_698705361 m1A Human chr22 + 19178684 19178684 19178684 GCGGGGCGCGGGGCGCGGGCATGGCGGGCGGGAGGCGGGGCGCCCTGTGGCGGCTTCGGGTCCGA GCGGGGCGCGGGGCGCGGGCATGGCGGGCGGGGGGCGGGGCGCCCTGTGGCGGCTTCGGGTCCGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr22:19178576..19178775 26863410 MeRIP-seq:(Medium) rs1555923641 Functional Loss SNV dbSNP153 33..33 33 - - - 98317 RMVar_ID_98317 Human_SNP_ID_698710679 m1A Human chr22 + 19197155 19197155 19197155 CTCTCCCTGGACAAGACCAGACGTCTGGTTACAGCCTGCTCAGCATGCAGAAAGCCTGGAGAAAC CTCTCCCTGGACAAGACCAGACGTCTGGTTACGGCCTGCTCAGCATGCAGAAAGCCTGGAGAAAC A G AC000072.1 Ensembl:ENSG00000286367 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19197107..19197191 26863196 MeRIP-seq:(Medium) rs1349059228 Functional Loss SNV dbSNP153 33..33 33 - - - 98318 RMVar_ID_98318 Human_SNP_ID_698710744 m1A Human chr22 + 19197448 19197448 19197448 GCCTGCAGCTCCATCCCACCTGCTTGCCTACCAAGGCCACAGCTCCGGTGACTCCTCATTTCTCT GCCTGCAGCTCCATCCCACCTGCTTGCCTACCGAGGCCACAGCTCCGGTGACTCCTCATTTCTCT A G AC000072.1 Ensembl:ENSG00000286367 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19197401..19197589 26863196 MeRIP-seq:(Medium) rs1233456197 Functional Loss SNV dbSNP153 33..33 33 - - - 98319 RMVar_ID_98319 Human_SNP_ID_698710752 m1A Human chr22 + 19197473 19197473 19197473 GCCTACCAAGGCCACAGCTCCGGTGACTCCTCATTTCTCTTCTGCCTTATTTTCACTCTCCACAG GCCTACCAAGGCCACAGCTCCGGTGACTCCTCGTTTCTCTTCTGCCTTATTTTCACTCTCCACAG A G AC000072.1 Ensembl:ENSG00000286367 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:19197367..19197612 26863196 MeRIP-seq:(Medium) rs879956148 Functional Loss SNV dbSNP153 33..33 33 - - - 98320 RMVar_ID_98320 Human_SNP_ID_698711971 m1A Human chr22 - 19202601 19202601 19202601 GAAGTAGGGTAGTGCAGTAGATGCCATGGATGACGGAAGGAGGGGAGGTGCCATGGATGATGGAA GAAGTAGGGTAGTGCAGTAGATGCCATGGATGGCGGAAGGAGGGGAGGTGCCATGGATGATGGAA T C CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19202594..19202727 26863196 MeRIP-seq:(Medium) rs1555940545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112,RMVar_hsa_circ_30437,RMVar_hsa_circ_42411,RMVar_hsa_circ_8410,RMVar_hsa_circ_17891 98321 RMVar_ID_98321 Human_SNP_ID_698712280 m1A Human chr22 + 19203938 19203938 19203938 ACCCGCCCTCACTGCTTCTCTCCTCACACCCCACTTGGCAGCACGCCCTGCCGGCTCTGCCTTCA ACCCGCCCTCACTGCTTCTCTCCTCACACCCCCCTTGGCAGCACGCCCTGCCGGCTCTGCCTTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19203916..19204183 26863196 MeRIP-seq:(Medium) rs1439257305 Functional Loss SNV dbSNP153 33..33 33 - - - 98322 RMVar_ID_98322 Human_SNP_ID_698712317 m1A Human chr22 - 19204085 19204085 19204085 TGGCTGCTATGCTACAAACAGAGTGAAGGACAAGGGTGGAGCAGGGAGTGCATAGAGGAGGATGG TGGCTGCTATGCTACAAACAGAGTGAAGGACACGGGTGGAGCAGGGAGTGCATAGAGGAGGATGG T G CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19203865..19204121 26863196 MeRIP-seq:(Medium) rs781938030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112,RMVar_hsa_circ_30437,RMVar_hsa_circ_42411,RMVar_hsa_circ_8410,RMVar_hsa_circ_17891 98323 RMVar_ID_98323 Human_SNP_ID_698721612 m1A Human chr22 - 19240418 19240418 19240418 TGTTTCCCTCCTCTCTCTGCCCGGCCAAACCCAGACCGCAAACCCAGACTGCCCCTCCACAGACA TGTTTCCCTCCTCTCTCTGCCCGGCCAAACCCTGACCGCAAACCCAGACTGCCCCTCCACAGACA T A CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19240416..19240487 26863196 MeRIP-seq:(Medium) rs919538537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207,RMVar_hsa_circ_38776,RMVar_hsa_circ_303597,RMVar_hsa_circ_351045,RMVar_hsa_circ_404,RMVar_hsa_circ_367577,RMVar_hsa_circ_283928 98324 RMVar_ID_98324 Human_SNP_ID_698743516 m1A Human chr22 - 19331400 19331400 19331400 CAGCCTGCCCTGGCTGCAGCAAGGGCAGGGCCACACTCTCGCCGCTGATGACATGCAGGACCGCC CAGCCTGCCCTGGCTGCAGCAAGGGCAGGGCCGCACTCTCGCCGCTGATGACATGCAGGACCGCC T C HIRA Ensembl:ENSG00000100084 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19331352..19331426 26863196 MeRIP-seq:(Medium) rs531266123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8545524,Human_RBP_ID_27491574 Human_miRNA_ID_940372,Human_miRNA_ID_1771199 98325 RMVar_ID_98325 Human_SNP_ID_698760112 m1A Human chr22 - 19401644 19401644 19401644 GATGGCTTCCCGGACTATGGTCCAAACAGTGGAAAGGATGCAGTGGCTGTAACCTGAAGCAGGAA GATGGCTTCCCGGACTATGGTCCAAACAGTGGGAAGGATGCAGTGGCTGTAACCTGAAGCAGGAA T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19401642..19401743 26863196 MeRIP-seq:(Medium) rs1191775681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14392550,Human_RBP_ID_27706695 RMVar_hsa_circ_32381,RMVar_hsa_circ_275365,RMVar_hsa_circ_11373,RMVar_hsa_circ_266928,RMVar_hsa_circ_297832,RMVar_hsa_circ_11423,RMVar_hsa_circ_319511,RMVar_hsa_circ_212933,RMVar_hsa_circ_212937,RMVar_hsa_circ_115706,RMVar_hsa_circ_212936,RMVar_hsa_circ_106195,RMVar_hsa_circ_35018,RMVar_hsa_circ_212938,RMVar_hsa_circ_212939,RMVar_hsa_circ_370319,RMVar_hsa_circ_77924,RMVar_hsa_circ_212942,RMVar_hsa_circ_212943,RMVar_hsa_circ_375414 98326 RMVar_ID_98326 Human_SNP_ID_698760177 m1A Human chr22 - 19401930 19401930 19401930 TGCGGGAGGCAGTGTGCCTTTGAGACCGTGGCAGAGGCTCTTCTCTGAGCAAGAATATGAAGTCT TGCGGGAGGCAGTGTGCCTTTGAGACCGTGGCGGAGGCTCTTCTCTGAGCAAGAATATGAAGTCT T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19401928..19402157 26863196 MeRIP-seq:(Medium) rs1278806278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_833055,Human_RBP_ID_9433025,Human_RBP_ID_14392568,Human_RBP_ID_17148293,Human_RBP_ID_18952325,Human_RBP_ID_22525761,Human_RBP_ID_22604066,Human_RBP_ID_24381107 RMVar_hsa_circ_32381,RMVar_hsa_circ_275365,RMVar_hsa_circ_11373,RMVar_hsa_circ_266928,RMVar_hsa_circ_297832,RMVar_hsa_circ_11423,RMVar_hsa_circ_319511,RMVar_hsa_circ_212933,RMVar_hsa_circ_212937,RMVar_hsa_circ_115706,RMVar_hsa_circ_212936,RMVar_hsa_circ_106195,RMVar_hsa_circ_35018,RMVar_hsa_circ_212938,RMVar_hsa_circ_212939,RMVar_hsa_circ_370319,RMVar_hsa_circ_77924,RMVar_hsa_circ_212942,RMVar_hsa_circ_212943,RMVar_hsa_circ_375414 98327 RMVar_ID_98327 Human_SNP_ID_698766073 m1A Human chr22 + 19426192 19426192 19426192 GATCTCCCTGTCTCCCTGAGCATCTCACCAAGACTAGAAATTCCTAACTCCTCTAGGGCCTGCCT GATCTCCCTGTCTCCCTGAGCATCTCACCAAGGCTAGAAATTCCTAACTCCTCTAGGGCCTGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19426190..19426554 26863196 MeRIP-seq:(Medium) rs142603816 Functional Loss SNV dbSNP153 33..33 33 - - - 98328 RMVar_ID_98328 Human_SNP_ID_698766266 m1A Human chr22 - 19427150 19427150 19427150 GGGACAAATCTGTTAAACATCGTATAGCATGCAGGACAGCCCACTCATGGAGAATTATCTAGCCC GGGACAAATCTGTTAAACATCGTATAGCATGCGGGACAGCCCACTCATGGAGAATTATCTAGCCC T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19427148..19427380 26863196 MeRIP-seq:(Medium) rs1422488808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7061854,Human_RBP_ID_14393409 RMVar_hsa_circ_212937,RMVar_hsa_circ_115706 98329 RMVar_ID_98329 Human_SNP_ID_698767420 m1A Human chr22 + 19431683 19431683 19431683 GCCGCCACCCGCGCTCGGCCGCCGCCGCCGCCACCACAGCCGCATCCCCTGCGCCGCTCCTCCTC GCCGCCACCCGCGCTCGGCCGCCGCCGCCGCCGCCACAGCCGCATCCCCTGCGCCGCTCCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr22:19431398..19447550;chr22:19431470..19431705;chr22:19431364..19447677 26863196 MeRIP-seq:(Medium) rs1326701747 Functional Loss SNV dbSNP153 33..33 33 - - - 98330 RMVar_ID_98330 Human_SNP_ID_698767815 m1A Human chr22 - 19432602 19432602 19432602 CGCTATCCGGCCAGCGTCCGCACTCACCCGCTAGTCGGGCGCAGGGCTAGCGAGATACTTCGCAG CGCTATCCGGCCAGCGTCCGCACTCACCCGCTGGTCGGGCGCAGGGCTAGCGAGATACTTCGCAG T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr22:19432551..19432708;chr22:19432501..19432675 26863196,26863410 MeRIP-seq:(Medium) rs1229520609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212937,RMVar_hsa_circ_115706 98331 RMVar_ID_98331 Human_SNP_ID_698771724 m1A Human chr22 - 19447491 19447491 19447491 ACCGCGCCGAGTGGAAGCTCTGCCGCAGCGCCAGGCACTTCCTACACCACTACTACGTCCACGGC ACCGCGCCGAGTGGAAGCTCTGCCGCAGCGCCGGGCACTTCCTACACCACTACTACGTCCACGGC T C C22orf39 Ensembl:ENSG00000242259 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19447444..19447671 26863196 MeRIP-seq:(Medium) rs751754548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708390,Human_RBP_ID_17399684 Human_Splice_Rec_2136994,Human_Splice_Rec_2137040,Human_Splice_Rec_2137044,Human_Splice_Rec_2137048,Human_Splice_Rec_2137052,Human_Splice_Rec_2137056 RMVar_hsa_circ_212937,RMVar_hsa_circ_115706,RMVar_hsa_circ_212952,RMVar_hsa_circ_109523 98332 RMVar_ID_98332 Human_SNP_ID_698775908 m1A Human chr22 - 19465276 19465276 19465276 CTTGCCATGTTGCCTTGACAGAATGTGTCTGCAGATTAGAAAACGCACTTAGGAACTTTGCCTGT CTTGCCATGTTGCCTTGACAGAATGTGTCTGCGGATTAGAAAACGCACTTAGGAACTTTGCCTGT T C UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:19465226..19465275 26863196 MeRIP-seq:(Medium) rs1420117611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1200672,Human_RBP_ID_9124449,Human_RBP_ID_14394083,Human_RBP_ID_25680357 Human_Splice_Rec_2137087,Human_Splice_Rec_2137109,Human_Splice_Rec_2137129,Human_Splice_Rec_2137141,Human_Splice_Rec_2137159,Human_Splice_Rec_2137175 RMVar_hsa_circ_7550,RMVar_hsa_circ_336707,RMVar_hsa_circ_64752,RMVar_hsa_circ_307987 98333 RMVar_ID_98333 Human_SNP_ID_698776523 m1A Human chr22 - 19467924 19467924 19467924 GAGCGTCAACCTTCAAGTGGCCACCTACTCCAAATTCCAACCTCAGAGCCCTGACTTCCTGGACA GAGCGTCAACCTTCAAGTGGCCACCTACTCCACATTCCAACCTCAGAGCCCTGACTTCCTGGACA T G UFD1 Ensembl:ENSG00000070010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:19467824..19468034;chr22:19467829..19468040;chr22:19467824..19468039 26863196 MeRIP-seq:(Medium) rs771636950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1028360,Human_RBP_ID_3961954,Human_RBP_ID_5504283,Human_RBP_ID_8116784,Human_RBP_ID_9299635,Human_RBP_ID_9391940,Human_RBP_ID_14394218,Human_RBP_ID_17285019,Human_RBP_ID_17398340,Human_RBP_ID_17982204,Human_RBP_ID_19007601,Human_RBP_ID_26822185 Human_Splice_Rec_2137084,Human_Splice_Rec_2137085,Human_Splice_Rec_2137106,Human_Splice_Rec_2137107,Human_Splice_Rec_2137126,Human_Splice_Rec_2137127,Human_Splice_Rec_2137156,Human_Splice_Rec_2137157,Human_Splice_Rec_2137172,Human_Splice_Rec_2137173,Human_Splice_Rec_2137186,Human_Splice_Rec_2137187,Human_Splice_Rec_2137196,Human_Splice_Rec_2137204,Human_Splice_Rec_2137208 Human_miRNA_ID_2354566,Human_miRNA_ID_3070368 RMVar_hsa_circ_7550,RMVar_hsa_circ_212956,RMVar_hsa_circ_336707,RMVar_hsa_circ_64752,RMVar_hsa_circ_307987,RMVar_hsa_circ_372083 98334 RMVar_ID_98334 Human_SNP_ID_698779256 m1A Human chr22 + 19479133 19479133 19479133 GCAGACTCCGCTCCTCTCAGGCAATGCAACGAAGAAACCCCGCCGACCGCTCTCCCAGCCGCCGC GCAGACTCCGCTCCTCTCAGGCAATGCAACGAGGAAACCCCGCCGACCGCTCTCCCAGCCGCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr22:19479024..19479200;chr22:19479010..19479200;chr22:19479007..19479200;chr22:19479076..19479150 26863196,32194978 MeRIP-seq:(Medium) rs777109877 Functional Loss SNV dbSNP153 33..33 33 - - - 98335 RMVar_ID_98335 Human_SNP_ID_698779265 m1A Human chr22 + 19479146 19479146 19479146 CTCTCAGGCAATGCAACGAAGAAACCCCGCCGACCGCTCTCCCAGCCGCCGCTGCCGCTGCCGCC CTCTCAGGCAATGCAACGAAGAAACCCCGCCGGCCGCTCTCCCAGCCGCCGCTGCCGCTGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19479035..19479200 26863196 MeRIP-seq:(Medium) rs1209629031 Functional Loss SNV dbSNP153 33..33 33 - - - 98336 RMVar_ID_98336 Human_SNP_ID_698779617 m1A Human chr22 - 19480009 19480009 19480009 GGGGTCCCGGACTGGGCGTCACCTGGCTCTGGACCACCTCGTAGAACTCTTTGCGGAAATCGGAC GGGGTCCCGGACTGGGCGTCACCTGGCTCTGGGCCACCTCGTAGAACTCTTTGCGGAAATCGGAC T C LINC00895 RNACentral:URS00008B7073 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19479959..19480141 26863196 MeRIP-seq:(Medium) rs141041145 Functional Loss SNV dbSNP153 33..33 33 - - - 98337 RMVar_ID_98337 Human_SNP_ID_698779713 m1A Human chr22 + 19480236 19480236 19480236 GCAAGATCCTTCAGGTGAGTTCTGCGGACCCTAGGAGGGCGGGGCCGGCGCGCGAGGTGAGGGTG GCAAGATCCTTCAGGTGAGTTCTGCGGACCCTGGGAGGGCGGGGCCGGCGCGCGAGGTGAGGGTG A G CDC45 Ensembl:ENSG00000093009 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19480210..19480311 26863196 MeRIP-seq:(Medium) rs549095792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19112650 Human_Splice_Rec_2137210,Human_Splice_Rec_2137248,Human_Splice_Rec_2137260,Human_Splice_Rec_2137298,Human_Splice_Rec_2137312,Human_Splice_Rec_2137350,Human_Splice_Rec_2137380,Human_Splice_Rec_2137416 RMVar_hsa_circ_50018,RMVar_hsa_circ_81370,RMVar_hsa_circ_15497,RMVar_hsa_circ_212959 98338 RMVar_ID_98338 Human_SNP_ID_698783386 m1A Human chr22 + 19494365 19494365 19494365 GTGGAGCAAACCATGCGGAGGAGGCAGCGGCGAGAGTGGGAGGCCCGGAGGTGAGTCTGTGCTTC GTGGAGCAAACCATGCGGAGGAGGCAGCGGCGGGAGTGGGAGGCCCGGAGGTGAGTCTGTGCTTC A G CDC45 Ensembl:ENSG00000093009 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19483901..19494498 26863196 MeRIP-seq:(Medium) rs1183144426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929146,Human_RBP_ID_3961960,Human_RBP_ID_9348341,Human_RBP_ID_9391947,Human_RBP_ID_19007605,Human_RBP_ID_22479699,Human_RBP_ID_22674949,Human_RBP_ID_23015554,Human_RBP_ID_26345003 Human_Splice_Rec_2137218,Human_Splice_Rec_2137219,Human_Splice_Rec_2137268,Human_Splice_Rec_2137269,Human_Splice_Rec_2137306,Human_Splice_Rec_2137307,Human_Splice_Rec_2137322,Human_Splice_Rec_2137323,Human_Splice_Rec_2137356,Human_Splice_Rec_2137357,Human_Splice_Rec_2137388,Human_Splice_Rec_2137389,Human_Splice_Rec_2137422,Human_Splice_Rec_2137423,Human_Splice_Rec_2137456,Human_Splice_Rec_2137457,Human_Splice_Rec_2137466,Human_Splice_Rec_2137467 RMVar_hsa_circ_15497,RMVar_hsa_circ_49622,RMVar_hsa_circ_125452,RMVar_hsa_circ_332809,RMVar_hsa_circ_52403,RMVar_hsa_circ_212962,RMVar_hsa_circ_212963,RMVar_hsa_circ_357057 98339 RMVar_ID_98339 Human_SNP_ID_698784141 m1A Human chr22 - 19497377 19497377 19497377 CAGCTCAAACATCACCATGGCTGACTGTAAGGAAGCAGAGAAGTCTAAGGCTCATGGGAGGGGCA CAGCTCAAACATCACCATGGCTGACTGTAAGGGAGCAGAGAAGTCTAAGGCTCATGGGAGGGGCA T C LINC00895 RNACentral:URS00008B7073 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:19497376..19497450 32194978 MeRIP-seq:(Medium) rs1194758869 Functional Loss SNV dbSNP153 33..33 33 - - - 98340 RMVar_ID_98340 Human_SNP_ID_698786318 m1A Human chr22 + 19506114 19506114 19506114 AGGAGATGGTCACTGCTTTCCAAGGCCACACAATAGTGGCTTGGCCCAAACTGCAGCAGTGGCTG AGGAGATGGTCACTGCTTTCCAAGGCCACACAGTAGTGGCTTGGCCCAAACTGCAGCAGTGGCTG A G CDC45 Ensembl:ENSG00000093009 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19506111..19506462 26863196 MeRIP-seq:(Medium) rs992126124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17193645,Human_RBP_ID_18168491 RMVar_hsa_circ_685,RMVar_hsa_circ_15497,RMVar_hsa_circ_375700,RMVar_hsa_circ_212964,RMVar_hsa_circ_119517,RMVar_hsa_circ_212965 98341 RMVar_ID_98341 Human_SNP_ID_698786319 m1A Human chr22 + 19506114 19506114 19506114 AGGAGATGGTCACTGCTTTCCAAGGCCACACAATAGTGGCTTGGCCCAAACTGCAGCAGTGGCTG AGGAGATGGTCACTGCTTTCCAAGGCCACACATTAGTGGCTTGGCCCAAACTGCAGCAGTGGCTG A T CDC45 Ensembl:ENSG00000093009 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19506111..19506462 26863196 MeRIP-seq:(Medium) rs992126124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17193645,Human_RBP_ID_18168491 RMVar_hsa_circ_685,RMVar_hsa_circ_15497,RMVar_hsa_circ_375700,RMVar_hsa_circ_212964,RMVar_hsa_circ_119517,RMVar_hsa_circ_212965 98342 RMVar_ID_98342 Human_SNP_ID_698786353 m1A Human chr22 - 19506223 19506223 19506223 ATGGCCACCTGACTACTGACGTGTCCACCCTCACTCTTCCTCCTTCCCAGCCATCACAGTGCAGA ATGGCCACCTGACTACTGACGTGTCCACCCTCGCTCTTCCTCCTTCCCAGCCATCACAGTGCAGA T C LINC00895 RNACentral:URS00008B7073 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:19506179..19506472 26863196 MeRIP-seq:(Medium) rs1038941781 Functional Loss SNV dbSNP153 33..33 33 - - - 98343 RMVar_ID_98343 Human_SNP_ID_698788729 m1A Human chr22 + 19516023 19516022 19516023 GGGTGTGGGTGCAGCAGGCACAGCAGAGAAGGAAACCCTAAACCTTTATCCTGAAGGAGCGTGCC GGGTGTGGGTGCAGCAGGCACAGCAGAGAAGG_AACCCTAAACCTTTATCCTGAAGGAGCGTGCC GA G CDC45 Ensembl:ENSG00000093009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19516019..19516406 26863196 MeRIP-seq:(Medium) rs1454493034 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_685,RMVar_hsa_circ_15497,RMVar_hsa_circ_102629,RMVar_hsa_circ_119517,RMVar_hsa_circ_212965,RMVar_hsa_circ_212966 98344 RMVar_ID_98344 Human_SNP_ID_698840537 m1A Human chr22 - 19714570 19714570 19714570 AGGCCTGTGCTCATGGTGGCCGCCGGCGGGGGACGTGCGGGGCGGGCTCGCGGGCGGGGCGCGAC AGGCCTGTGCTCATGGTGGCCGCCGGCGGGGGGCGTGCGGGGCGGGCTCGCGGGCGGGGCGCGAC T C lnc-GNB1L-1,lnc-GNB1L-1:2,lnc-GNB1L-1:3 RNACentral:URS00008BEC50,RNACentral:URS00008BFFF0,RNACentral:URS00009B749D lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr22:19714522..19714706;chr22:19714529..19714644 26863196 MeRIP-seq:(Medium) rs975237803 Functional Loss SNV dbSNP153 33..33 33 - - - 98345 RMVar_ID_98345 Human_SNP_ID_698842258 m1A Human chr22 - 19720092 19720092 19720092 CTGATGCGCTCTACGGGGAAGGGGCCACTGGAAGGGCCTCTCCAACCCTCAGCCCCTCACCCTTG CTGATGCGCTCTACGGGGAAGGGGCCACTGGAGGGGCCTCTCCAACCCTCAGCCCCTCACCCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19720087..19720234 26863196 MeRIP-seq:(Medium) rs944417816 Functional Loss SNV dbSNP153 33..33 33 - - - 98346 RMVar_ID_98346 Human_SNP_ID_698842580 m1A Human chr22 + 19720863 19720863 19720863 GAGGATGAGGACTTCAAGCAGCAGGACCGGGAACTGAAGGTGAACATGCAGACTGGTGGGGCAGG GAGGATGAGGACTTCAAGCAGCAGGACCGGGAGCTGAAGGTGAACATGCAGACTGGTGGGGCAGG A G AC000093.1,SEPTIN5 Ensembl:ENSG00000284874,Ensembl:ENSG00000184702 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19720751..19721750 26863196 MeRIP-seq:(Medium) rs1223453363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_781683,Human_RBP_ID_929158,Human_RBP_ID_3962758,Human_RBP_ID_26345023 Human_Splice_Rec_2137530,Human_Splice_Rec_2137531,Human_Splice_Rec_2137552,Human_Splice_Rec_2137553,Human_Splice_Rec_2137574,Human_Splice_Rec_2137575,Human_Splice_Rec_2137590,Human_Splice_Rec_2137591,Human_Splice_Rec_2137608,Human_Splice_Rec_2137609,Human_Splice_Rec_2137624,Human_Splice_Rec_2137625,Human_Splice_Rec_2137644,Human_Splice_Rec_2137645,Human_Splice_Rec_2137662,Human_Splice_Rec_2137670,Human_Splice_Rec_2137674,Human_Splice_Rec_2137675,Human_Splice_Rec_2137678,Human_Splice_Rec_2137679,Human_Splice_Rec_2137698,Human_Splice_Rec_2137699,Human_Splice_Rec_2137720,Human_Splice_Rec_2137721 RMVar_hsa_circ_93049,RMVar_hsa_circ_122027,RMVar_hsa_circ_212969,RMVar_hsa_circ_212970 98347 RMVar_ID_98347 Human_SNP_ID_698853296 m1A Human chr22 - 19754255 19754255 19754255 GGATGGGGTAATGGGTGGAGAGAAGACTGGACAGGGAAGCACACAGCCGTGTGACACCAGCCTCC GGATGGGGTAATGGGTGGAGAGAAGACTGGACGGGGAAGCACACAGCCGTGTGACACCAGCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19754204..19754383 26863196 MeRIP-seq:(Medium) rs908989631 Functional Loss SNV dbSNP153 33..33 33 - - - 98348 RMVar_ID_98348 Human_SNP_ID_698853550 m1A Human chr22 - 19755217 19755217 19755217 GAGGAGCGGGAGCGGGAGCCGGCACGGGAGCGAGCTGGGATCTGCATCAAAGCCGGGTCGGACAT GAGGAGCGGGAGCGGGAGCCGGCACGGGAGCGGGCTGGGATCTGCATCAAAGCCGGGTCGGACAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19755168..19755317 26863196 MeRIP-seq:(Medium) rs932897827 Functional Loss SNV dbSNP153 33..33 33 - - - 98349 RMVar_ID_98349 Human_SNP_ID_698854017 m1A Human chr22 - 19756781 19756781 19756781 CACGCGGGTTCCGCACGCGAACGCAGCGCCTCAGCACGGCCCGCGGCAAGTGTTCCTCCCTCCCT CACGCGGGTTCCGCACGCGAACGCAGCGCCTCGGCACGGCCCGCGGCAAGTGTTCCTCCCTCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19756732..19756937 26863196 MeRIP-seq:(Medium) rs994321861 Functional Loss SNV dbSNP153 33..33 33 - - - 98350 RMVar_ID_98350 Human_SNP_ID_698854154 m1A Human chr22 - 19757133 19757133 19757133 GGCCGACCCTACCCCACCGGCTGCCTATACTCACTCGCTTGATTTCGGACCCCCGGACCCCGTTG GGCCGACCCTACCCCACCGGCTGCCTATACTCGCTCGCTTGATTTCGGACCCCCGGACCCCGTTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19757020..19757172 26863196 MeRIP-seq:(Medium) rs917412576 Functional Loss SNV dbSNP153 33..33 33 - - - 98351 RMVar_ID_98351 Human_SNP_ID_698854955 m1A Human chr22 + 19759665 19759665 19759665 CCCCGGCAGGGATGCACTTCAGCACCGTCACCAGGGACATGGAAGGTGAGCCTCCAGGCCGTGTC CCCCGGCAGGGATGCACTTCAGCACCGTCACCGGGGACATGGAAGGTGAGCCTCCAGGCCGTGTC A G TBX1 Ensembl:ENSG00000184058 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19759616..19759731 26863196 MeRIP-seq:(Medium) rs28649236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2137735,Human_Splice_Rec_2137751,Human_Splice_Rec_2137767 98352 RMVar_ID_98352 Human_SNP_ID_698855224 m1A Human chr22 + 19760490 19760490 19760490 AGGAAAAGAACGTCTGGGAGAGAGAGAGGAGAAACGCACGCGGGCGGGCGGCAGAGCGAGGGCCG AGGAAAAGAACGTCTGGGAGAGAGAGAGGAGAGACGCACGCGGGCGGGCGGCAGAGCGAGGGCCG A G TBX1 Ensembl:ENSG00000184058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19760313..19760504 26863196 MeRIP-seq:(Medium) rs1197357681 Functional Loss SNV dbSNP153 33..33 33 - - - 98353 RMVar_ID_98353 Human_SNP_ID_698855319 m1A Human chr22 - 19760680 19760680 19760680 GCGCCCCGCCCCGCCCCGCCCGGGGCCCCCCCACCCCCGCGCGGAGACAATGGACTAGATCCCTC GCGCCCCGCCCCGCCCCGCCCGGGGCCCCCCCCCCCCCGCGCGGAGACAATGGACTAGATCCCTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:19760582..19760711 26863196 MeRIP-seq:(Medium) rs1185121811 Functional Loss SNV dbSNP153 33..33 33 - - - 98354 RMVar_ID_98354 Human_SNP_ID_698856067 m1A Human chr22 - 19762647 19762647 19762647 TGATAAGAGTCTCCCCACCTTCCTCAGGGCACAGGGCAAGCTTCCACTCCCCTTAAGACACATAA TGATAAGAGTCTCCCCACCTTCCTCAGGGCACCGGGCAAGCTTCCACTCCCCTTAAGACACATAA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:19762535..19762673 26863196 MeRIP-seq:(Medium) rs41298806 Functional Loss SNV dbSNP153 33..33 33 - - - 98355 RMVar_ID_98355 Human_SNP_ID_698857401 m1A Human chr22 - 19766462 19766462 19766462 GAGGGGCTTAGCACCCGGGCCAGCAGCTGCGGAGGATGCGCCGGGTCCCCGAGCACTGCTGGCCC GAGGGGCTTAGCACCCGGGCCAGCAGCTGCGGTGGATGCGCCGGGTCCCCGAGCACTGCTGGCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19766412..19766713 32194978 MeRIP-seq:(Medium) rs1390758133 Functional Loss SNV dbSNP153 33..33 33 - - - 98356 RMVar_ID_98356 Human_SNP_ID_698857618 m1A Human chr22 + 19766762 19766762 19766762 CATCCGCACCACCACCACCACCCCGTGAGTCCAGCCGCCGCGGCCGCCGCCGCCGCTGCCGCAGC CATCCGCACCACCACCACCACCCCGTGAGTCCGGCCGCCGCGGCCGCCGCCGCCGCTGCCGCAGC A G TBX1 Ensembl:ENSG00000184058 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:19766662..19766763 26863410 MeRIP-seq:(Medium) rs553461195 Functional Loss SNV dbSNP153 33..33 33 - - - 98357 RMVar_ID_98357 Human_SNP_ID_698857672 m1A Human chr22 + 19766809 19766809 19766809 CGCCGCCGCTGCCGCAGCTGCCGCGGCCGCCAACATGTACTCGTCGGCCGGAGCCGCGCCGCCCG CGCCGCCGCTGCCGCAGCTGCCGCGGCCGCCAGCATGTACTCGTCGGCCGGAGCCGCGCCGCCCG A G TBX1 Ensembl:ENSG00000184058 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr22:19766525..19766950 26863410 MeRIP-seq:(Medium) rs1443840436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27304302 98358 RMVar_ID_98358 Human_SNP_ID_698857683 m1A Human chr22 + 19766828 19766828 19766828 GCCGCGGCCGCCAACATGTACTCGTCGGCCGGAGCCGCGCCGCCCGGCTCCTACGACTATTGCCC GCCGCGGCCGCCAACATGTACTCGTCGGCCGGGGCCGCGCCGCCCGGCTCCTACGACTATTGCCC A G TBX1 Ensembl:ENSG00000184058 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr22:19766251..19767062;chr22:19766777..19766999 26863410,26863196 MeRIP-seq:(Medium) rs1229395713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575402,Human_RBP_ID_18168918,Human_RBP_ID_18497020 98359 RMVar_ID_98359 Human_SNP_ID_698865355 m1A Human chr22 + 19796721 19796721 19796721 GGAAGACAATGTCTTCTTGCACCAGGGAGCCCAGCTGGACAGTCACCTCTGGAAACAGGCTCCAT GGAAGACAATGTCTTCTTGCACCAGGGAGCCCGGCTGGACAGTCACCTCTGGAAACAGGCTCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19796718..19796802 26863196 MeRIP-seq:(Medium) rs1184909954 Functional Loss SNV dbSNP153 33..33 33 - - - 98360 RMVar_ID_98360 Human_SNP_ID_698877365 m1A Human chr22 + 19846324 19846324 19846324 GTCAAAGGCAGAAAGTTACAACCTGGGAATACAGGATAATGCCTTTGTACCCCCCAGGTAGGGAA GTCAAAGGCAGAAAGTTACAACCTGGGAATACCGGATAATGCCTTTGTACCCCCCAGGTAGGGAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19802100..19854640 32194978 MeRIP-seq:(Medium) rs1379574672 Functional Loss SNV dbSNP153 33..33 33 - - - 98361 RMVar_ID_98361 Human_SNP_ID_698878395 m1A Human chr22 - 19850351 19850351 19850351 TTGCGGATTCAGCACTTAAGCCCTAGTGTGTAAATGACTTGGATCTCCCTCCTGGCAGACTGTGA TTGCGGATTCAGCACTTAAGCCCTAGTGTGTATATGACTTGGATCTCCCTCCTGGCAGACTGTGA T A GNB1L,RTL10 Ensembl:ENSG00000185838,Ensembl:ENSG00000215012 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19850310..19850381 26863196 MeRIP-seq:(Medium) rs1569057557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1306780,Human_RBP_ID_4709884,Human_RBP_ID_14397026,Human_RBP_ID_18784504,Human_RBP_ID_22087106 Human_miRNA_ID_1786963 RMVar_hsa_circ_55021 98362 RMVar_ID_98362 Human_SNP_ID_698879112 m1A Human chr22 + 19852283 19852283 19852283 CCACGAGGCATGCTGGGAGCACAGGGGAGAAGAGAGGAGAGCCAGCACTGGTGGGTGGTGGGGGT CCACGAGGCATGCTGGGAGCACAGGGGAGAAGGGAGGAGAGCCAGCACTGGTGGGTGGTGGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19852233..19852360 26863196 MeRIP-seq:(Medium) rs770925442 Functional Loss SNV dbSNP153 33..33 33 - - - 98363 RMVar_ID_98363 Human_SNP_ID_698879294 m1A Human chr22 + 19853044 19853044 19853044 ATTAGGCTCTTTTACATCCCAGCACCAGGCACACAGCAGGTCCTACCTGCTTCCCCGACAGAGCA ATTAGGCTCTTTTACATCCCAGCACCAGGCACGCAGCAGGTCCTACCTGCTTCCCCGACAGAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19853038..19853665 26863196 MeRIP-seq:(Medium) rs901741874 Functional Loss SNV dbSNP153 33..33 33 - - - 98364 RMVar_ID_98364 Human_SNP_ID_698879680 m1A Human chr22 + 19854487 19854487 19854487 GAATCGCCCGCGAAGAGGGTCCTGGGATCCGTAGCCACAGACCGTGGGACGGGCCTCCCTCTGAG GAATCGCCCGCGAAGAGGGTCCTGGGATCCGTCGCCACAGACCGTGGGACGGGCCTCCCTCTGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19854415..19854639 26863196 MeRIP-seq:(Medium) rs951381676 Functional Loss SNV dbSNP153 33..33 33 - - - 98365 RMVar_ID_98365 Human_SNP_ID_698879681 m1A Human chr22 + 19854487 19854487 19854487 GAATCGCCCGCGAAGAGGGTCCTGGGATCCGTAGCCACAGACCGTGGGACGGGCCTCCCTCTGAG GAATCGCCCGCGAAGAGGGTCCTGGGATCCGTGGCCACAGACCGTGGGACGGGCCTCCCTCTGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19854415..19854639 26863196 MeRIP-seq:(Medium) rs951381676 Functional Loss SNV dbSNP153 33..33 33 - - - 98366 RMVar_ID_98366 Human_SNP_ID_698879697 m1A Human chr22 + 19854526 19854526 19854526 GACCGTGGGACGGGCCTCCCTCTGAGGGCGAGAGTCCAGGCGCCACCTAGAAAGTGGAGAACGAG GACCGTGGGACGGGCCTCCCTCTGAGGGCGAGCGTCCAGGCGCCACCTAGAAAGTGGAGAACGAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:19821372..19854640 26863410 MeRIP-seq:(Medium) rs1477074798 Functional Loss SNV dbSNP153 33..33 33 - - - 98367 RMVar_ID_98367 Human_SNP_ID_698879781 m1A Human chr22 + 19854746 19854746 19854746 GTGCCCCTCTGCGGATCAGAAGTCGGGAAAAGACGCAGGGGCGCAGCTCCAGGCCCGCGTGCACG GTGCCCCTCTGCGGATCAGAAGTCGGGAAAAGGCGCAGGGGCGCAGCTCCAGGCCCGCGTGCACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19854698..19854808 26863196 MeRIP-seq:(Medium) rs1162360818 Functional Loss SNV dbSNP153 33..33 33 - - - 98368 RMVar_ID_98368 Human_SNP_ID_698885612 m1A Human chr22 - 19877487 19877487 19877487 AGGCAGGACTGTGCCTAGCAGGGGAGGATGGAACAGCAGGAAGCCAGGCCAGGGCAAGCCAGGGC AGGCAGGACTGTGCCTAGCAGGGGAGGATGGAGCAGCAGGAAGCCAGGCCAGGGCAAGCCAGGGC T C TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19877479..19877669 26863196 MeRIP-seq:(Medium) rs997425006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28721,RMVar_hsa_circ_76860,RMVar_hsa_circ_212972 98369 RMVar_ID_98369 Human_SNP_ID_698886400 m1A Human chr22 - 19880209 19880209 19880209 TATGGCTGTGTGGGGCTGTCCGAGGAGGAGGCAGTGGCTCGCCACGGGCAGGAGCATGTTGAGGT TATGGCTGTGTGGGGCTGTCCGAGGAGGAGGCGGTGGCTCGCCACGGGCAGGAGCATGTTGAGGT T C TXNRD2 Ensembl:ENSG00000184470 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19876014..19880983 32194978 MeRIP-seq:(Medium) rs1164473318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3961986,Human_RBP_ID_5119857,Human_RBP_ID_19007610,Human_RBP_ID_19112670,Human_RBP_ID_22454322 Human_Splice_Rec_2137904,Human_Splice_Rec_2137905,Human_Splice_Rec_2137928,Human_Splice_Rec_2137929,Human_Splice_Rec_2137962,Human_Splice_Rec_2137963,Human_Splice_Rec_2137994,Human_Splice_Rec_2137995,Human_Splice_Rec_2138006,Human_Splice_Rec_2138007,Human_Splice_Rec_2138018,Human_Splice_Rec_2138019,Human_Splice_Rec_2138034,Human_Splice_Rec_2138035,Human_Splice_Rec_2138068,Human_Splice_Rec_2138069,Human_Splice_Rec_2138100,Human_Splice_Rec_2138101,Human_Splice_Rec_2138132,Human_Splice_Rec_2138133,Human_Splice_Rec_2138142,Human_Splice_Rec_2138143,Human_Splice_Rec_2138152,Human_Splice_Rec_2138153,Human_Splice_Rec_2138166,Human_Splice_Rec_2138167,Human_Splice_Rec_2138176,Human_Splice_Rec_2138177 RMVar_hsa_circ_28721,RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973 98370 RMVar_ID_98370 Human_SNP_ID_698886406 m1A Human chr22 + 19880233 19880233 19880233 CGAGCCACTGCCTCCTCCTCGGACAGCCCCACACAGCCATACTCCAGCGGGGTGAAGACGGTCGT CGAGCCACTGCCTCCTCCTCGGACAGCCCCACGCAGCCATACTCCAGCGGGGTGAAGACGGTCGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19880133..19880282 26863196 MeRIP-seq:(Medium) rs1390827449 Functional Loss SNV dbSNP153 33..33 33 - - - 98371 RMVar_ID_98371 Human_SNP_ID_698894536 m1A Human chr22 - 19909670 19909668 19909670 TGTGTGAGCAGTGTGTGTGAGTAGTGTGTGTGAGTGGTGTGTGTGTGAATGGTGTGTGTATGTGA TGTGTGAGCAGTGTGTGTGAGTAGTGTGTGTG__TGGTGTGTGTGTGAATGGTGTGTGTATGTGA ACT A TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19909501..19910058 26863196 MeRIP-seq:(Medium) rs150132889 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3678226,Human_RBP_ID_5240736,Human_RBP_ID_5298216,Human_RBP_ID_5653332,Human_RBP_ID_17286607,Human_RBP_ID_23115718,Human_RBP_ID_23935575,Human_RBP_ID_27841222 RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973,RMVar_hsa_circ_330209,RMVar_hsa_circ_212975 98372 RMVar_ID_98372 Human_SNP_ID_698894538 m1A Human chr22 - 19909670 19909670 19909670 TGTGTGAGCAGTGTGTGTGAGTAGTGTGTGTGAGTGGTGTGTGTGTGAATGGTGTGTGTATGTGA TGTGTGAGCAGTGTGTGTGAGTAGTGTGTGTGTGTGGTGTGTGTGTGAATGGTGTGTGTATGTGA T A TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19909501..19910058 26863196 MeRIP-seq:(Medium) rs866997117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3678226,Human_RBP_ID_5240736,Human_RBP_ID_5298216,Human_RBP_ID_5653332,Human_RBP_ID_17286607,Human_RBP_ID_23115718,Human_RBP_ID_23935575,Human_RBP_ID_27841222 RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973,RMVar_hsa_circ_330209,RMVar_hsa_circ_212975 98373 RMVar_ID_98373 Human_SNP_ID_698894559 m1A Human chr22 - 19909696 19909696 19909696 GGTGTGTGTGCGTGGTGTGTGTGGTGTGTGTGAGCAGTGTGTGTGAGTAGTGTGTGTGAGTGGTG GGTGTGTGTGCGTGGTGTGTGTGGTGTGTGTGTGCAGTGTGTGTGAGTAGTGTGTGTGAGTGGTG T A TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19909514..19910055 26863196 MeRIP-seq:(Medium) rs1196408991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3678226,Human_RBP_ID_5240736,Human_RBP_ID_5298392,Human_RBP_ID_5653332,Human_RBP_ID_17286607,Human_RBP_ID_23115718,Human_RBP_ID_23954980,Human_RBP_ID_27841222 RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973,RMVar_hsa_circ_330209,RMVar_hsa_circ_212975 98374 RMVar_ID_98374 Human_SNP_ID_698896963 m1A Human chr22 - 19918219 19918219 19918219 TGTGGATTTTACATTTTGTTTCGTATCTTCACAGGAGGAAGATGGCAGAAGCTGTTCAAAATCAC TGTGGATTTTACATTTTGTTTCGTATCTTCACGGGAGGAAGATGGCAGAAGCTGTTCAAAATCAC T C TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19918174..19931080 32194978 MeRIP-seq:(Medium) rs775877650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_930501,Human_RBP_ID_3962787,Human_RBP_ID_26345695 Human_Splice_Rec_2137887,Human_Splice_Rec_2137945,Human_Splice_Rec_2137977,Human_Splice_Rec_2138051,Human_Splice_Rec_2138083,Human_Splice_Rec_2138115,Human_Splice_Rec_2138185,Human_Splice_Rec_2138207,Human_Splice_Rec_2138229,Human_Splice_Rec_2138255,Human_Splice_Rec_2138275 RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973 98375 RMVar_ID_98375 Human_SNP_ID_698897210 m1A Human chr22 - 19918950 19918950 19918950 CACCTGCGTCAACGTGGGCTGCATCCCCAAGAAGCTGATGCACCAGGCGGCACTGCTGGGAGGCC CACCTGCGTCAACGTGGGCTGCATCCCCAAGAGGCTGATGCACCAGGCGGCACTGCTGGGAGGCC T C TXNRD2 Ensembl:ENSG00000184470 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19918901..19919066 26863196 MeRIP-seq:(Medium) rs897456386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_929186,Human_RBP_ID_3962007,Human_RBP_ID_4685672,Human_RBP_ID_17989123,Human_RBP_ID_19007616 Human_Splice_Rec_2137884,Human_Splice_Rec_2137885,Human_Splice_Rec_2137942,Human_Splice_Rec_2137943,Human_Splice_Rec_2137974,Human_Splice_Rec_2137975,Human_Splice_Rec_2138048,Human_Splice_Rec_2138049,Human_Splice_Rec_2138080,Human_Splice_Rec_2138081,Human_Splice_Rec_2138112,Human_Splice_Rec_2138113,Human_Splice_Rec_2138204,Human_Splice_Rec_2138205,Human_Splice_Rec_2138226,Human_Splice_Rec_2138227,Human_Splice_Rec_2138272,Human_Splice_Rec_2138273 RMVar_hsa_circ_76860,RMVar_hsa_circ_35396,RMVar_hsa_circ_111966,RMVar_hsa_circ_212972,RMVar_hsa_circ_212973 98376 RMVar_ID_98376 Human_SNP_ID_698899911 m1A Human chr22 + 19927794 19927794 19927794 TGTGGGTGCTTCAGGGCCAACTGCCTGACTCCAGTATGCACAAATTTCAGTGTCCATGGATTCTG TGTGGGTGCTTCAGGGCCAACTGCCTGACTCCGGTATGCACAAATTTCAGTGTCCATGGATTCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:19927764..19927891 26863196 MeRIP-seq:(Medium) rs1046049160 Functional Loss SNV dbSNP153 33..33 33 - - - 98377 RMVar_ID_98377 Human_SNP_ID_698900708 m1A Human chr22 - 19930976 19930976 19930976 TGGCAAGGCCTCGAAGCTTTTAGGGCCCCTAGAGAGGGTGGTGCTGTCCAGAAAACGTCCATGAG TGGCAAGGCCTCGAAGCTTTTAGGGCCCCTAGCGAGGGTGGTGCTGTCCAGAAAACGTCCATGAG T G TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19930974..19931170 26863196 MeRIP-seq:(Medium) rs369553856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35396 98378 RMVar_ID_98378 Human_SNP_ID_698902419 m1A Human chr22 - 19936648 19936648 19936648 ACAACCAGAGTGGCAGGGGTGTCCCTGCATGAAGAAGGGTACAGAGAAGCAGGTTGAGTGGATGG ACAACCAGAGTGGCAGGGGTGTCCCTGCATGACGAAGGGTACAGAGAAGCAGGTTGAGTGGATGG T G TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:19936645..19936784 26863196 MeRIP-seq:(Medium) rs1432026449 Functional Loss SNV dbSNP153 33..33 33 - - - 98379 RMVar_ID_98379 Human_SNP_ID_698909501 m1A Human chr22 + 19962780 19962780 19962780 CGTGCTGGAGGCCATTGACACCTACTGCGAGCAGAAGGAGTGGGCCATGAACGTGGGCGACAAGA CGTGCTGGAGGCCATTGACACCTACTGCGAGCCGAAGGAGTGGGCCATGAACGTGGGCGACAAGA A C COMT Ensembl:ENSG00000093010 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19962308..19962825 32194978 MeRIP-seq:(Medium) rs1324928849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575480,Human_RBP_ID_931612,Human_RBP_ID_9391952,Human_RBP_ID_19008504,Human_RBP_ID_22086236,Human_RBP_ID_22454549,Human_RBP_ID_22673948,Human_RBP_ID_22768086 Human_Splice_Rec_2138283,Human_Splice_Rec_2138291,Human_Splice_Rec_2138301,Human_Splice_Rec_2138313,Human_Splice_Rec_2138327,Human_Splice_Rec_2138337,Human_Splice_Rec_2138347,Human_Splice_Rec_2138353 Human_miRNA_ID_2709357 RMVar_hsa_circ_37887,RMVar_hsa_circ_288933,RMVar_hsa_circ_212976 98380 RMVar_ID_98380 Human_SNP_ID_698909804 m1A Human chr22 + 19963672 19963671 19963672 TCAGCTGTGCGCATGGCCCGCCTGCTGTCACCAGGGGCGAGGCTCATCACCATCGAGATCAACCC TCAGCTGTGCGCATGGCCCGCCTGCTGTCACC_GGGGCGAGGCTCATCACCATCGAGATCAACCC CA C COMT Ensembl:ENSG00000093010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19963624..19963700 26863196 MeRIP-seq:(Medium) rs1209420360 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_151804,Human_RBP_ID_3962013,Human_RBP_ID_4708809,Human_RBP_ID_5204147,Human_RBP_ID_5241189,Human_RBP_ID_5323937,Human_RBP_ID_18193968,Human_RBP_ID_18471553,Human_RBP_ID_22086237,Human_RBP_ID_22454550,Human_RBP_ID_22768088,Human_RBP_ID_26822210 Human_Splice_Rec_2138285,Human_Splice_Rec_2138293,Human_Splice_Rec_2138303,Human_Splice_Rec_2138315,Human_Splice_Rec_2138329,Human_Splice_Rec_2138339,Human_Splice_Rec_2138349,Human_Splice_Rec_2138355,Human_Splice_Rec_2138361,Human_Splice_Rec_2138363 Human_miRNA_ID_2209637,Human_miRNA_ID_2437408,Human_miRNA_ID_3034243 RMVar_hsa_circ_212977,RMVar_hsa_circ_37887,RMVar_hsa_circ_288933,RMVar_hsa_circ_212976,RMVar_hsa_circ_295748,RMVar_hsa_circ_371439,RMVar_hsa_circ_212978 98381 RMVar_ID_98381 Human_SNP_ID_698909806 m1A Human chr22 + 19963672 19963672 19963672 TCAGCTGTGCGCATGGCCCGCCTGCTGTCACCAGGGGCGAGGCTCATCACCATCGAGATCAACCC TCAGCTGTGCGCATGGCCCGCCTGCTGTCACCCGGGGCGAGGCTCATCACCATCGAGATCAACCC A C COMT Ensembl:ENSG00000093010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19963624..19963700 26863196 MeRIP-seq:(Medium) rs763613355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151804,Human_RBP_ID_3962013,Human_RBP_ID_4708809,Human_RBP_ID_5204147,Human_RBP_ID_5241189,Human_RBP_ID_5323937,Human_RBP_ID_18193968,Human_RBP_ID_18471553,Human_RBP_ID_22086237,Human_RBP_ID_22454550,Human_RBP_ID_22768088,Human_RBP_ID_26822210 Human_Splice_Rec_2138285,Human_Splice_Rec_2138293,Human_Splice_Rec_2138303,Human_Splice_Rec_2138315,Human_Splice_Rec_2138329,Human_Splice_Rec_2138339,Human_Splice_Rec_2138349,Human_Splice_Rec_2138355,Human_Splice_Rec_2138361,Human_Splice_Rec_2138363 Human_miRNA_ID_2209637,Human_miRNA_ID_2437408,Human_miRNA_ID_3034243 RMVar_hsa_circ_212977,RMVar_hsa_circ_37887,RMVar_hsa_circ_288933,RMVar_hsa_circ_212976,RMVar_hsa_circ_295748,RMVar_hsa_circ_371439,RMVar_hsa_circ_212978 98382 RMVar_ID_98382 Human_SNP_ID_698909851 m1A Human chr22 - 19963761 19963761 19963761 TTTCCAGGTCTGACAACGGGTCAGGCATGCACACCTTGTCCTTCACGCCAGCGAAATCCACCATC TTTCCAGGTCTGACAACGGGTCAGGCATGCACTCCTTGTCCTTCACGCCAGCGAAATCCACCATC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19963726..19963775 32194978 MeRIP-seq:(Medium) rs1272343407 Functional Loss SNV dbSNP153 33..33 33 - - - 98383 RMVar_ID_98383 Human_SNP_ID_698909852 m1A Human chr22 - 19963761 19963761 19963761 TTTCCAGGTCTGACAACGGGTCAGGCATGCACACCTTGTCCTTCACGCCAGCGAAATCCACCATC TTTCCAGGTCTGACAACGGGTCAGGCATGCACGCCTTGTCCTTCACGCCAGCGAAATCCACCATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19963726..19963775 32194978 MeRIP-seq:(Medium) rs1272343407 Functional Loss SNV dbSNP153 33..33 33 - - - 98384 RMVar_ID_98384 Human_SNP_ID_698911450 m1A Human chr22 + 19968646 19968646 19968646 CACGTGCGCGGGAGCAGCTGCTTTGAGTGCACACACTACCAATCGTTCCTGGAATACAGGGAGGT CACGTGCGCGGGAGCAGCTGCTTTGAGTGCACCCACTACCAATCGTTCCTGGAATACAGGGAGGT A C COMT Ensembl:ENSG00000093010 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:19968595..19968890 26863196 MeRIP-seq:(Medium) rs1411474800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575488,Human_RBP_ID_1381978,Human_RBP_ID_1607996,Human_RBP_ID_5472816,Human_RBP_ID_8545865,Human_RBP_ID_9124502,Human_RBP_ID_9333164,Human_RBP_ID_17982308,Human_RBP_ID_22454556,Human_RBP_ID_22819499 98385 RMVar_ID_98385 Human_SNP_ID_698912054 m1A Human chr22 - 19970662 19970662 19970662 CCACCCTGAGCAGATCGTGCCGTGGAGCTTGGAGCCCCCTGGCGGCAGGGGTTGGCAGCGCCTCG CCACCCTGAGCAGATCGTGCCGTGGAGCTTGGGGCCCCCTGGCGGCAGGGGTTGGCAGCGCCTCG T C ARVCF Ensembl:ENSG00000099889 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19970542..19971263 32194978 MeRIP-seq:(Medium) rs1464656809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529751,Human_RBP_ID_23015556,Human_RBP_ID_23212866 Human_Splice_Rec_2138404,Human_Splice_Rec_2138426 98386 RMVar_ID_98386 Human_SNP_ID_698914803 m1A Human chr22 - 19977905 19977905 19977905 CCTCATACCAAGGGCTGGAGAGACGATCATGCAGGTCCCAGGAGGCTGGAACTGTGGGAGCAGCA CCTCATACCAAGGGCTGGAGAGACGATCATGCCGGTCCCAGGAGGCTGGAACTGTGGGAGCAGCA T G ARVCF Ensembl:ENSG00000099889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19977894..19978064 26863196 MeRIP-seq:(Medium) rs1229848436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23532,RMVar_hsa_circ_48736,RMVar_hsa_circ_61889,RMVar_hsa_circ_100175,RMVar_hsa_circ_96183,RMVar_hsa_circ_212982,RMVar_hsa_circ_212983 98387 RMVar_ID_98387 Human_SNP_ID_698915170 m1A Human chr22 - 19978997 19978991 19978997 ACCATGGCCTGCAGACGCTGACCCACGAGGTGATCGTGCCCCACTCAGGATGGGAGCGTGAGCCC ACCATGGCCTGCAGACGCTGACCCACGAGGTG______CCCCACTCAGGATGGGAGCGTGAGCCC GCACGAT G ARVCF Ensembl:ENSG00000099889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19971961..19979370 32194978 MeRIP-seq:(Medium) rs756735382 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_5240741,Human_RBP_ID_22086787,Human_RBP_ID_23212867 Human_Splice_Rec_2138378,Human_Splice_Rec_2138434,Human_Splice_Rec_2138466,Human_Splice_Rec_2138496 RMVar_hsa_circ_23532,RMVar_hsa_circ_48736,RMVar_hsa_circ_61889,RMVar_hsa_circ_96183,RMVar_hsa_circ_212982 98388 RMVar_ID_98388 Human_SNP_ID_100558511 m1A Human chr2 + 165940461 165940461 165940461 GGCTCACTCCCACCCTTTGTCTCAGACCTCACACCTTACTCACCTCTCTTACTCCTTCCCACTCC GGCTCACTCCCACCCTTTGTCTCAGACCTCACGCCTTACTCACCTCTCTTACTCCTTCCCACTCC A G TTC21B-AS1 Ensembl:ENSG00000224490 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:165940312..165940583 26863196 MeRIP-seq:(Medium) rs980581914 Functional Loss SNV dbSNP153 33..33 33 - - - 98389 RMVar_ID_98389 Human_SNP_ID_100558512 m1A Human chr2 + 165940461 165940461 165940461 GGCTCACTCCCACCCTTTGTCTCAGACCTCACACCTTACTCACCTCTCTTACTCCTTCCCACTCC GGCTCACTCCCACCCTTTGTCTCAGACCTCACTCCTTACTCACCTCTCTTACTCCTTCCCACTCC A T TTC21B-AS1 Ensembl:ENSG00000224490 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:165940312..165940583 26863196 MeRIP-seq:(Medium) rs980581914 Functional Loss SNV dbSNP153 33..33 33 - - - 98390 RMVar_ID_98390 Human_SNP_ID_100559034 m1A Human chr2 - 165942569 165942569 165942569 CAAAGTGGGTTGAGTAAAGAGAACAGAAGTGAAGGCCTGAGGAAGAAAGGTGGGATGGGGGTGAG CAAAGTGGGTTGAGTAAAGAGAACAGAAGTGATGGCCTGAGGAAGAAAGGTGGGATGGGGGTGAG T A TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:165942564..165942692 26863196 MeRIP-seq:(Medium) rs911345000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15149,RMVar_hsa_circ_9382,RMVar_hsa_circ_18038,RMVar_hsa_circ_26357,RMVar_hsa_circ_63483,RMVar_hsa_circ_330939,RMVar_hsa_circ_334570,RMVar_hsa_circ_204321,RMVar_hsa_circ_72062,RMVar_hsa_circ_124689,RMVar_hsa_circ_204325 98391 RMVar_ID_98391 Human_SNP_ID_100561894 m1A Human chr2 + 165953716 165953716 165953716 CCTTCAATTCCTGCGAGTCCATGGCTGCCCCGAGGCCGGGCCGCGGGGCTCTGGGGATTGTCTCG CCTTCAATTCCTGCGAGTCCATGGCTGCCCCGCGGCCGGGCCGCGGGGCTCTGGGGATTGTCTCG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:165953637..165953715 32194978 MeRIP-seq:(Medium) rs1257211563 Functional Loss SNV dbSNP153 33..33 33 - - - 98392 RMVar_ID_98392 Human_SNP_ID_100561895 m1A Human chr2 + 165953716 165953716 165953716 CCTTCAATTCCTGCGAGTCCATGGCTGCCCCGAGGCCGGGCCGCGGGGCTCTGGGGATTGTCTCG CCTTCAATTCCTGCGAGTCCATGGCTGCCCCGGGGCCGGGCCGCGGGGCTCTGGGGATTGTCTCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:165953637..165953715 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 98393 RMVar_ID_98393 Human_SNP_ID_100603426 m1A Human chr2 + 166127960 166127960 166127960 AGACACACAAACACACACAAACGCACACATACACACATGCACCAGAGACCTCTGCAGTATCCTCT AGACACACAAACACACACAAACGCACACATACGCACATGCACCAGAGACCTCTGCAGTATCCTCT A G SCN1A-AS1 Ensembl:ENSG00000236107 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:166127899..166127984 26863196 MeRIP-seq:(Medium) rs1419604545 Functional Loss SNV dbSNP153 33..33 33 - - - 98394 RMVar_ID_98394 Human_SNP_ID_100648998 m1A Human chr2 - 166311785 166311785 166311785 TTTCCATCCAGGCCTCTTATGTGAGGAGCTGAAGAGGAATTAAAATATACAGGATGAAAAGATGG TTTCCATCCAGGCCTCTTATGTGAGGAGCTGAGGAGGAATTAAAATATACAGGATGAAAAGATGG T C SCN9A Ensembl:ENSG00000169432 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:166311689..166311863 26863196 MeRIP-seq:(Medium) rs200356611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9387624 Human_Splice_Rec_318284,Human_Splice_Rec_318332,Human_Splice_Rec_318380,Human_Splice_Rec_318428,Human_Splice_Rec_318602,Human_Splice_Rec_318630,Human_Splice_Rec_318648 RMVar_hsa_circ_37304,RMVar_hsa_circ_293042,RMVar_hsa_circ_329964,RMVar_hsa_circ_56570,RMVar_hsa_circ_204341,RMVar_hsa_circ_204342,RMVar_hsa_circ_50035,RMVar_hsa_circ_204347,RMVar_hsa_circ_319287,RMVar_hsa_circ_204349,RMVar_hsa_circ_367632,RMVar_hsa_circ_354456 98395 RMVar_ID_98395 Human_SNP_ID_100649005 m1A Human chr2 - 166311799 166311799 166311799 TCTTTATTTCTTTGTTTCCATCCAGGCCTCTTATGTGAGGAGCTGAAGAGGAATTAAAATATACA TCTTTATTTCTTTGTTTCCATCCAGGCCTCTTCTGTGAGGAGCTGAAGAGGAATTAAAATATACA T G SCN9A Ensembl:ENSG00000169432 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:166311786..166311856 26863196 MeRIP-seq:(Medium) rs113850984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4585364,Human_RBP_ID_9387624 Human_Splice_Rec_318284,Human_Splice_Rec_318332,Human_Splice_Rec_318380,Human_Splice_Rec_318428,Human_Splice_Rec_318602,Human_Splice_Rec_318630,Human_Splice_Rec_318648 RMVar_hsa_circ_37304,RMVar_hsa_circ_293042,RMVar_hsa_circ_329964,RMVar_hsa_circ_56570,RMVar_hsa_circ_204341,RMVar_hsa_circ_204342,RMVar_hsa_circ_50035,RMVar_hsa_circ_204347,RMVar_hsa_circ_319287,RMVar_hsa_circ_204349,RMVar_hsa_circ_367632,RMVar_hsa_circ_354456 98396 RMVar_ID_98396 Human_SNP_ID_100664595 m1A Human chr2 - 166375810 166375810 166375810 AGCGGCAGGCGTCCCCTGAGCAACAGGAGCCCAGAGAAAAAGAAGCAGCCCTGAGAGAGCGCCGG AGCGGCAGGCGTCCCCTGAGCAACAGGAGCCCGGAGAAAAAGAAGCAGCCCTGAGAGAGCGCCGG T C SCN9A Ensembl:ENSG00000169432 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:166375719..166375930 26863196 MeRIP-seq:(Medium) rs1484213614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4585371,Human_RBP_ID_5528092,Human_RBP_ID_9387627,Human_RBP_ID_18421928 Human_Splice_Rec_318627 98397 RMVar_ID_98397 Human_SNP_ID_100664605 m1A Human chr2 + 166375843 166375843 166375843 GGGCTCCTGTTGCTCAGGGGACGCCTGCCGCTAGCAGCCACTGGCACCCAGGCTAGCCCAGCCTC GGGCTCCTGTTGCTCAGGGGACGCCTGCCGCTGGCAGCCACTGGCACCCAGGCTAGCCCAGCCTC A G SCN1A-AS1 Ensembl:ENSG00000236107 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:166375793..166375881 26863196 MeRIP-seq:(Medium) rs889946230 Functional Loss SNV dbSNP153 33..33 33 - - - 98398 RMVar_ID_98398 Human_SNP_ID_100902885 m1A Human chr2 + 167293166 167293166 167293166 GGCGCTGCCGGTCTTGCAGGCGGCCGCCGGGGAGGGGCGGCCGAGAGAGCGGAGCACGAGGAGGC GGCGCTGCCGGTCTTGCAGGCGGCCGCCGGGGGGGGGCGGCCGAGAGAGCGGAGCACGAGGAGGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:167293085..167293172 26863410 MeRIP-seq:(Medium) rs983144040 Functional Loss SNV dbSNP153 33..33 33 - - - 98399 RMVar_ID_98399 Human_SNP_ID_100902889 m1A Human chr2 + 167293177 167293177 167293177 TCTTGCAGGCGGCCGCCGGGGAGGGGCGGCCGAGAGAGCGGAGCACGAGGAGGCGGGGGCGGCAG TCTTGCAGGCGGCCGCCGGGGAGGGGCGGCCGGGAGAGCGGAGCACGAGGAGGCGGGGGCGGCAG A G AC073050.1 Ensembl:ENSG00000228222 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:167293126..167293197 26863196 MeRIP-seq:(Medium) rs868133496 Functional Loss SNV dbSNP153 33..33 33 - - - 98400 RMVar_ID_98400 Human_SNP_ID_101072962 m1A Human chr2 - 167970087 167970087 167970087 GCAGAAACTGAAAGAAAGGGAGGGAGGCAGTCATGGAGTCATGGAGGAAGAACATTTCCGGGAGA GCAGAAACTGAAAGAAAGGGAGGGAGGCAGTCGTGGAGTCATGGAGGAAGAACATTTCCGGGAGA T C STK39 Ensembl:ENSG00000198648 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:167969847..167970267 26863196 MeRIP-seq:(Medium) rs897809622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204359,RMVar_hsa_circ_123659,RMVar_hsa_circ_33075,RMVar_hsa_circ_264789 98401 RMVar_ID_98401 Human_SNP_ID_101097628 m1A Human chr2 - 168075164 168075164 168075164 TAAAACCGAAGACGGGGACTGGGAGTGGAGTGACGACGAGATGGATGAGAAGAGCGAAGAAGGGA TAAAACCGAAGACGGGGACTGGGAGTGGAGTGGCGACGAGATGGATGAGAAGAGCGAAGAAGGGA T C STK39 Ensembl:ENSG00000198648 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:168065369..168075227 26863196 MeRIP-seq:(Medium) rs1186114001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918887,Human_RBP_ID_6845310 Human_Splice_Rec_319112,Human_Splice_Rec_319113,Human_Splice_Rec_319146,Human_Splice_Rec_319147 RMVar_hsa_circ_36306,RMVar_hsa_circ_204359,RMVar_hsa_circ_123659,RMVar_hsa_circ_276600,RMVar_hsa_circ_33075,RMVar_hsa_circ_264789,RMVar_hsa_circ_290356,RMVar_hsa_circ_316039,RMVar_hsa_circ_322832,RMVar_hsa_circ_86659,RMVar_hsa_circ_204364,RMVar_hsa_circ_204365,RMVar_hsa_circ_204366,RMVar_hsa_circ_282571,RMVar_hsa_circ_285123,RMVar_hsa_circ_297585,RMVar_hsa_circ_333528,RMVar_hsa_circ_304353,RMVar_hsa_circ_292225,RMVar_hsa_circ_108804,RMVar_hsa_circ_98957,RMVar_hsa_circ_204370,RMVar_hsa_circ_204372,RMVar_hsa_circ_204374,RMVar_hsa_circ_204375,RMVar_hsa_circ_204373,RMVar_hsa_circ_204371,RMVar_hsa_circ_95217,RMVar_hsa_circ_266574,RMVar_hsa_circ_268982,RMVar_hsa_circ_362809,RMVar_hsa_circ_363698,RMVar_hsa_circ_291260,RMVar_hsa_circ_204376 98402 RMVar_ID_98402 Human_SNP_ID_101097629 m1A Human chr2 + 168075166 168075166 168075166 CCTTCTTCGCTCTTCTCATCCATCTCGTCGTCACTCCACTCCCAGTCCCCGTCTTCGGTTTTATG CCTTCTTCGCTCTTCTCATCCATCTCGTCGTCGCTCCACTCCCAGTCCCCGTCTTCGGTTTTATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:168075116..168075217 26863196 MeRIP-seq:(Medium) rs201897996 Functional Loss SNV dbSNP153 33..33 33 - - - 98403 RMVar_ID_98403 Human_SNP_ID_101097632 m1A Human chr2 - 168075179 168075179 168075179 AAGTGGTCACCTTCATAAAACCGAAGACGGGGACTGGGAGTGGAGTGACGACGAGATGGATGAGA AAGTGGTCACCTTCATAAAACCGAAGACGGGGGCTGGGAGTGGAGTGACGACGAGATGGATGAGA T C STK39 Ensembl:ENSG00000198648 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:168075133..168075210 26863196 MeRIP-seq:(Medium) rs768321414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918887,Human_RBP_ID_6845310 Human_Splice_Rec_319112,Human_Splice_Rec_319113,Human_Splice_Rec_319146,Human_Splice_Rec_319147 RMVar_hsa_circ_36306,RMVar_hsa_circ_204359,RMVar_hsa_circ_123659,RMVar_hsa_circ_276600,RMVar_hsa_circ_33075,RMVar_hsa_circ_264789,RMVar_hsa_circ_290356,RMVar_hsa_circ_316039,RMVar_hsa_circ_322832,RMVar_hsa_circ_86659,RMVar_hsa_circ_204364,RMVar_hsa_circ_204365,RMVar_hsa_circ_204366,RMVar_hsa_circ_282571,RMVar_hsa_circ_285123,RMVar_hsa_circ_297585,RMVar_hsa_circ_333528,RMVar_hsa_circ_304353,RMVar_hsa_circ_292225,RMVar_hsa_circ_108804,RMVar_hsa_circ_98957,RMVar_hsa_circ_204370,RMVar_hsa_circ_204372,RMVar_hsa_circ_204374,RMVar_hsa_circ_204375,RMVar_hsa_circ_204373,RMVar_hsa_circ_204371,RMVar_hsa_circ_95217,RMVar_hsa_circ_266574,RMVar_hsa_circ_268982,RMVar_hsa_circ_362809,RMVar_hsa_circ_363698,RMVar_hsa_circ_291260,RMVar_hsa_circ_204376 98404 RMVar_ID_98404 Human_SNP_ID_101102170 m1A Human chr2 + 168094496 168094496 168094496 TTGAAAAATCACCCACTTGCACTTCTTCATCCATTCACTCATTAATTCTGACTGTCCAACTTTTT TTGAAAAATCACCCACTTGCACTTCTTCATCCTTTCACTCATTAATTCTGACTGTCCAACTTTTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:168094494..168094633 26863196 MeRIP-seq:(Medium) rs116525822 Functional Loss SNV dbSNP153 33..33 33 - - - 98405 RMVar_ID_98405 Human_SNP_ID_101139043 m1A Human chr2 + 168247434 168247434 168247434 GGACGTGCACGGGCGAGCCGCTCGGCTCCGCCATGATGCTGCGGAGGAGAGCAGGAGGACGCGCC GGACGTGCACGGGCGAGCCGCTCGGCTCCGCCGTGATGCTGCGGAGGAGAGCAGGAGGACGCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:168247384..168247547 26863196 MeRIP-seq:(Medium) rs1192175185 Functional Loss SNV dbSNP153 33..33 33 - - - 98406 RMVar_ID_98406 Human_SNP_ID_101139056 m1A Human chr2 + 168247454 168247454 168247454 CTCGGCTCCGCCATGATGCTGCGGAGGAGAGCAGGAGGACGCGCCGGCCGACGGACGACCTTCCA CTCGGCTCCGCCATGATGCTGCGGAGGAGAGCGGGAGGACGCGCCGGCCGACGGACGACCTTCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:168247403..168247542 26863196 MeRIP-seq:(Medium) rs1339975131 Functional Loss SNV dbSNP153 33..33 33 - - - 98407 RMVar_ID_98407 Human_SNP_ID_101187299 m1A Human chr2 - 168456414 168456414 168456414 TGCTTTGTCCACTCCTGTCCTGCGGCACCCGCAGCCCGCCAAGCTCTCCACCGCGCAGGGCGCCC TGCTTTGTCCACTCCTGTCCTGCGGCACCCGCGGCCCGCCAAGCTCTCCACCGCGCAGGGCGCCC T C lnc-STK39-3,lnc-STK39-3:2,lnc-STK39-3:3,lnc-STK39-3:4,lnc-STK39-3:5,lnc-STK39-3:6,lnc-STK39-3:7,lnc-STK39-3:8,lnc-STK39-3:9 RNACentral:URS0000D57DA7,RNACentral:URS0000D5C280,RNACentral:URS0000D5B40F,RNACentral:URS0000D59253,RNACentral:URS0000D5E22C,RNACentral:URS0000D5B5F4,RNACentral:URS0000D5C0CE,RNACentral:URS0000D582D9,RNACentral:URS0000D57D23 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:168456260..168456477 26863196 MeRIP-seq:(Medium) rs781139328 Functional Loss SNV dbSNP153 33..33 33 - - - 98408 RMVar_ID_98408 Human_SNP_ID_101187300 m1A Human chr2 - 168456414 168456414 168456414 TGCTTTGTCCACTCCTGTCCTGCGGCACCCGCAGCCCGCCAAGCTCTCCACCGCGCAGGGCGCCC TGCTTTGTCCACTCCTGTCCTGCGGCACCCGCCGCCCGCCAAGCTCTCCACCGCGCAGGGCGCCC T G lnc-STK39-3,lnc-STK39-3:2,lnc-STK39-3:3,lnc-STK39-3:4,lnc-STK39-3:5,lnc-STK39-3:6,lnc-STK39-3:7,lnc-STK39-3:8,lnc-STK39-3:9 RNACentral:URS0000D57DA7,RNACentral:URS0000D5C280,RNACentral:URS0000D5B40F,RNACentral:URS0000D59253,RNACentral:URS0000D5E22C,RNACentral:URS0000D5B5F4,RNACentral:URS0000D5C0CE,RNACentral:URS0000D582D9,RNACentral:URS0000D57D23 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:168456260..168456477 26863196 MeRIP-seq:(Medium) rs781139328 Functional Loss SNV dbSNP153 33..33 33 - - - 98409 RMVar_ID_98409 Human_SNP_ID_101285469 m1A Human chr2 - 168862360 168862360 168862360 ATCTTGTGTTGCCACAGCCTGTGACATTAGCCAAAGCACCTAACCTTCCTGTGTATCAGTCTCCT ATCTTGTGTTGCCACAGCCTGTGACATTAGCCGAAGCACCTAACCTTCCTGTGTATCAGTCTCCT T C SPC25 Ensembl:ENSG00000152253 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:168862261..168862517 26863196 MeRIP-seq:(Medium) rs1378820037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13667692,Human_RBP_ID_23835345 98410 RMVar_ID_98410 Human_SNP_ID_101285492 m1A Human chr2 - 168862446 168862446 168862446 GGGTACATCTCTAATCACTTTCCATCACTGACATTCTACCCTAGTGTGCACTGTGATTAGGAGCA GGGTACATCTCTAATCACTTTCCATCACTGACGTTCTACCCTAGTGTGCACTGTGATTAGGAGCA T C SPC25 Ensembl:ENSG00000152253 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:168862244..168862519 26863196 MeRIP-seq:(Medium) rs1415541821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2600922,Human_RBP_ID_13667697,Human_RBP_ID_17134833,Human_RBP_ID_22422840 98411 RMVar_ID_98411 Human_SNP_ID_101293148 m1A Human chr2 + 168890370 168890370 168890370 CCCGCCGCCTTCCCCACACCAGATCCGCGCCCACTCTAGCCAACAGCCGGACTCTAGGCTCAGCT CCCGCCGCCTTCCCCACACCAGATCCGCGCCCGCTCTAGCCAACAGCCGGACTCTAGGCTCAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:168884887..168890431 26863196 MeRIP-seq:(Medium) rs1290082213 Functional Loss SNV dbSNP153 33..33 33 - - - 98412 RMVar_ID_98412 Human_SNP_ID_101410217 m1A Human chr2 + 169358681 169358681 169358681 AAGCTGATACTAACTCTTAAAAACATTACCACATTTTTATTGGATTAAAGAATATAATGTTGGAC AAGCTGATACTAACTCTTAAAAACATTACCACGTTTTTATTGGATTAAAGAATATAATGTTGGAC A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:169358676..169358803 26863196 MeRIP-seq:(Medium) rs565686885 Functional Loss SNV dbSNP153 33..33 33 - - - 98413 RMVar_ID_98413 Human_SNP_ID_101456668 m1A Human chr2 - 169528863 169528859 169528863 GAGCAGGGATGGCCAATGAGGTAGGAGGAAGGAAGGTAAGTAATACTTCCTAGAAGCCAAGTGGA GAGCAGGGATGGCCAATGAGGTAGGAGGAAGG____TAAGTAATACTTCCTAGAAGCCAAGTGGA ACCTT A FASTKD1 Ensembl:ENSG00000138399 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:169528812..169529050;chr2:169528813..169528956 26863196 MeRIP-seq:(Medium) rs999630740 Functional Loss DEL dbSNP153 33..36 33 - - - 98414 RMVar_ID_98414 Human_SNP_ID_101468536 m1A Human chr2 + 169573763 169573763 169573763 AGAAGTCAGGGTTATTCCTGGTCCCAACACGGAACGAAACAGGCTCGGATGTCTCGCCCAACCCT AGAAGTCAGGGTTATTCCTGGTCCCAACACGGTACGAAACAGGCTCGGATGTCTCGCCCAACCCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:169573712..169573828 26863196 MeRIP-seq:(Medium) rs1322075834 Functional Loss SNV dbSNP153 33..33 33 - - - 98415 RMVar_ID_98415 Human_SNP_ID_101468540 m1A Human chr2 + 169573771 169573771 169573771 GGGTTATTCCTGGTCCCAACACGGAACGAAACAGGCTCGGATGTCTCGCCCAACCCTCATATCTC GGGTTATTCCTGGTCCCAACACGGAACGAAACGGGCTCGGATGTCTCGCCCAACCCTCATATCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:169573723..169573797 26863196 MeRIP-seq:(Medium) rs1003585208 Functional Loss SNV dbSNP153 33..33 33 - - - 98416 RMVar_ID_98416 Human_SNP_ID_101471707 m1A Human chr2 + 169584440 169584440 169584440 CTTTAGCGCCTTTTCTGGCGGCGGTAGATTTGAAGCGCTTCAAAGGACCGGACCCAGAGAAGAGG CTTTAGCGCCTTTTCTGGCGGCGGTAGATTTGGAGCGCTTCAAAGGACCGGACCCAGAGAAGAGG A G PPIG Ensembl:ENSG00000138398 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:169584389..169584585 26863196 MeRIP-seq:(Medium) rs1457510054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067980,Human_RBP_ID_1579603,Human_RBP_ID_4623686,Human_RBP_ID_13668701,Human_RBP_ID_18421936,Human_RBP_ID_18749031,Human_RBP_ID_19000341,Human_RBP_ID_22076682,Human_RBP_ID_22997481,Human_RBP_ID_24545886 Human_Splice_Rec_320263,Human_Splice_Rec_320283,Human_Splice_Rec_320309,Human_Splice_Rec_320333,Human_Splice_Rec_320347,Human_Splice_Rec_320369 RMVar_hsa_circ_267844 98417 RMVar_ID_98417 Human_SNP_ID_101486109 m1A Human chr2 - 169636157 169636157 169636157 ATTCTTTGAGCTCTCTGCATCTCTTGCCTCCAATGTGGAGGAGTCTCACTACGTCTGAAACGATC ATTCTTTGAGCTCTCTGCATCTCTTGCCTCCAGTGTGGAGGAGTCTCACTACGTCTGAAACGATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:169636107..169636208 32194978 MeRIP-seq:(Medium) rs1303664853 Functional Loss SNV dbSNP153 33..33 33 - - - 98418 RMVar_ID_98418 Human_SNP_ID_101486431 m1A Human chr2 + 169637089 169637089 169637089 GAAGAGGACGGTCACGAAGCCGAGAGAGAAGAACACCACCAGGAAGATCAAGAAGTAAAGATAGG GAAGAGGACGGTCACGAAGCCGAGAGAGAAGACCACCACCAGGAAGATCAAGAAGTAAAGATAGG A C PPIG Ensembl:ENSG00000138398 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:169636207..169637268 26863196 MeRIP-seq:(Medium) rs199817037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9393,Human_RBP_ID_61295,Human_RBP_ID_243722,Human_RBP_ID_6847149,Human_RBP_ID_18412812,Human_RBP_ID_18533358,Human_RBP_ID_22743031,Human_RBP_ID_22996887,Human_RBP_ID_24545897,Human_RBP_ID_26340051 98419 RMVar_ID_98419 Human_SNP_ID_101500143 m1A Human chr2 - 169694327 169694327 169694327 GCCACAGTCACTTTTCCAGATCTAGGAGCATCATGGACACCTCGTCAGAGATGCTGGTACGGTTT GCCACAGTCACTTTTCCAGATCTAGGAGCATCGTGGACACCTCGTCAGAGATGCTGGTACGGTTT T C CCDC173 Ensembl:ENSG00000154479 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:169694249..169694361 26863196 MeRIP-seq:(Medium) rs766958436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623687 Human_Splice_Rec_320447,Human_Splice_Rec_320463 98420 RMVar_ID_98420 Human_SNP_ID_101527212 m1A Human chr2 + 169798974 169798974 169798974 CTGTGGCGCGGCTTCTGTGGGCCGGAACCTTAAAGGTGAGTAACTCTCGGTGGCTAATGAGAAGC CTGTGGCGCGGCTTCTGTGGGCCGGAACCTTAGAGGTGAGTAACTCTCGGTGGCTAATGAGAAGC A G SSB Ensembl:ENSG00000138385 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:169798896..169799398 32194978 MeRIP-seq:(Medium) rs1439543137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775899,Human_RBP_ID_922038,Human_RBP_ID_4623694,Human_RBP_ID_5471298,Human_RBP_ID_5528733,Human_RBP_ID_8852127,Human_RBP_ID_9296843,Human_RBP_ID_9331212,Human_RBP_ID_9385042,Human_RBP_ID_19101984,Human_RBP_ID_26341518 Human_Splice_Rec_320575,Human_Splice_Rec_320597,Human_Splice_Rec_320607,Human_Splice_Rec_320615 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471 98421 RMVar_ID_98421 Human_SNP_ID_101528909 m1A Human chr2 + 169805456 169805456 169805456 TGGAGTCCATATTATACAGTGTTCTGAAATACATTGTAATTATCTCACAGTATTATTTTGGCGAC TGGAGTCCATATTATACAGTGTTCTGAAATACCTTGTAATTATCTCACAGTATTATTTTGGCGAC A C SSB Ensembl:ENSG00000138385 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:169805451..169805550;chr2:169805451..169805475 26863196 MeRIP-seq:(Medium) rs1299520086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82825,RMVar_hsa_circ_25681,RMVar_hsa_circ_355579,RMVar_hsa_circ_204471,RMVar_hsa_circ_352264 98422 RMVar_ID_98422 Human_SNP_ID_101528910 m1A Human chr2 + 169805456 169805456 169805456 TGGAGTCCATATTATACAGTGTTCTGAAATACATTGTAATTATCTCACAGTATTATTTTGGCGAC TGGAGTCCATATTATACAGTGTTCTGAAATACGTTGTAATTATCTCACAGTATTATTTTGGCGAC A G SSB Ensembl:ENSG00000138385 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:169805451..169805550;chr2:169805451..169805475 26863196 MeRIP-seq:(Medium) rs1299520086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82825,RMVar_hsa_circ_25681,RMVar_hsa_circ_355579,RMVar_hsa_circ_204471,RMVar_hsa_circ_352264 98423 RMVar_ID_98423 Human_SNP_ID_101530359 m1A Human chr2 + 169810971 169810971 169810971 AACAAAGAAGTGACTTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGAAGCACTGAAGAAAATAAT AACAAAGAAGTGACTTGGGAAGTACTAGAAGGGGAGGTGGAAAAAGAAGCACTGAAGAAAATAAT A G SSB Ensembl:ENSG00000138385 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:169810920..169811035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_59139,Human_RBP_ID_205440,Human_RBP_ID_242869,Human_RBP_ID_829486,Human_RBP_ID_922050,Human_RBP_ID_1902066,Human_RBP_ID_2601261,Human_RBP_ID_3602955,Human_RBP_ID_5588756,Human_RBP_ID_6847538,Human_RBP_ID_8234702,Human_RBP_ID_9385055,Human_RBP_ID_18533365,Human_RBP_ID_22072935,Human_RBP_ID_24545902,Human_RBP_ID_26340060,Human_RBP_ID_27817746 Human_Splice_Rec_320593,Human_Splice_Rec_320639 Human_miRNA_ID_2842574 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471,RMVar_hsa_circ_376954 98424 RMVar_ID_98424 Human_SNP_ID_101530360 m1A Human chr2 + 169810971 169810971 169810971 AACAAAGAAGTGACTTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGAAGCACTGAAGAAAATAAT AACAAAGAAGTGACTTGGGAAGTACTAGAAGGTGAGGTGGAAAAAGAAGCACTGAAGAAAATAAT A T SSB Ensembl:ENSG00000138385 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:169810920..169811035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_59139,Human_RBP_ID_205440,Human_RBP_ID_242869,Human_RBP_ID_829486,Human_RBP_ID_922050,Human_RBP_ID_1902066,Human_RBP_ID_2601261,Human_RBP_ID_3602955,Human_RBP_ID_5588756,Human_RBP_ID_6847538,Human_RBP_ID_8234702,Human_RBP_ID_9385055,Human_RBP_ID_18533365,Human_RBP_ID_22072935,Human_RBP_ID_24545902,Human_RBP_ID_26340060,Human_RBP_ID_27817746 Human_Splice_Rec_320593,Human_Splice_Rec_320639 Human_miRNA_ID_2842574 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471,RMVar_hsa_circ_376954 98425 RMVar_ID_98425 Human_SNP_ID_101530369 m1A Human chr2 + 169810985 169810985 169810985 TTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGAAGCACTGAAGAAAATAATAGAAGACCAACAAG TTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGCAGCACTGAAGAAAATAATAGAAGACCAACAAG A C SSB Ensembl:ENSG00000138385 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:169810877..169811026 26863196 MeRIP-seq:(Medium) rs777853278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_205441,Human_RBP_ID_242869,Human_RBP_ID_829486,Human_RBP_ID_922050,Human_RBP_ID_1902066,Human_RBP_ID_3602955,Human_RBP_ID_5588756,Human_RBP_ID_6847538,Human_RBP_ID_8234702,Human_RBP_ID_8257354,Human_RBP_ID_9385055,Human_RBP_ID_18515456,Human_RBP_ID_18533365,Human_RBP_ID_24545902,Human_RBP_ID_26340060,Human_RBP_ID_27817746 Human_Splice_Rec_320593,Human_Splice_Rec_320639 Human_miRNA_ID_2842574 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471,RMVar_hsa_circ_376954 98426 RMVar_ID_98426 Human_SNP_ID_101530456 m1A Human chr2 + 169811269 169811264 169811270 GTAAAGGAAAAGTACAGTTTCAGGGCAAGAAAACGAAATTTGCTAGTGATGATGAACATGATGAA GTAAAGGAAAAGTACAGTTTCAGGGCAA______GAAATTTGCTAGTGATGATGAACATGATGAA AGAAAAC A SSB Ensembl:ENSG00000138385 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:169811220..169811337 26863196 MeRIP-seq:(Medium) rs1439778417 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_59140,Human_RBP_ID_1902068,Human_RBP_ID_2672486,Human_RBP_ID_6847543,Human_RBP_ID_8504467,Human_RBP_ID_9387650,Human_RBP_ID_13671307,Human_RBP_ID_18749130,Human_RBP_ID_22504663,Human_RBP_ID_23115066,Human_RBP_ID_23835965,Human_RBP_ID_24546198,Human_RBP_ID_26338733,Human_RBP_ID_27002571,Human_RBP_ID_27817749 Human_Splice_Rec_320594,Human_Splice_Rec_320595,Human_Splice_Rec_320640,Human_Splice_Rec_320641 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471,RMVar_hsa_circ_38545,RMVar_hsa_circ_376954 98427 RMVar_ID_98427 Human_SNP_ID_101534080 m1A Human chr2 - 169824626 169824626 169824626 CAATAGATTTCTCCGCAGATCCTGTGCCTTCAAACCCTACGAGTCCATACTTTAAAACAAAATGA CAATAGATTTCTCCGCAGATCCTGTGCCTTCAGACCCTACGAGTCCATACTTTAAAACAAAATGA T C METTL5 Ensembl:ENSG00000138382 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:169824575..169824864 26863196 MeRIP-seq:(Medium) rs760625136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_537400,Human_RBP_ID_777040,Human_RBP_ID_1298157,Human_RBP_ID_1376003,Human_RBP_ID_4622746,Human_RBP_ID_5378801,Human_RBP_ID_6847584,Human_RBP_ID_18749144,Human_RBP_ID_23835996 Human_Splice_Rec_320664,Human_Splice_Rec_320686,Human_Splice_Rec_320708,Human_Splice_Rec_320722,Human_Splice_Rec_320738,Human_Splice_Rec_320758,Human_Splice_Rec_320770,Human_Splice_Rec_320774 98428 RMVar_ID_98428 Human_SNP_ID_101534081 m1A Human chr2 - 169824626 169824626 169824626 CAATAGATTTCTCCGCAGATCCTGTGCCTTCAAACCCTACGAGTCCATACTTTAAAACAAAATGA CAATAGATTTCTCCGCAGATCCTGTGCCTTCACACCCTACGAGTCCATACTTTAAAACAAAATGA T G METTL5 Ensembl:ENSG00000138382 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:169824575..169824864 26863196 MeRIP-seq:(Medium) rs760625136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_537400,Human_RBP_ID_777040,Human_RBP_ID_1298157,Human_RBP_ID_1376003,Human_RBP_ID_4622746,Human_RBP_ID_5378801,Human_RBP_ID_6847584,Human_RBP_ID_18749144,Human_RBP_ID_23835996 Human_Splice_Rec_320664,Human_Splice_Rec_320686,Human_Splice_Rec_320708,Human_Splice_Rec_320722,Human_Splice_Rec_320738,Human_Splice_Rec_320758,Human_Splice_Rec_320770,Human_Splice_Rec_320774 98429 RMVar_ID_98429 Human_SNP_ID_101534097 m1A Human chr2 - 169824692 169824690 169824693 CGGGTCCGGCCAGCGGTGCTGAAAAAGGGAGAAGGTTGGGGGTAGGGAGGAAACAAGATCCCAGT CGGGTCCGGCCAGCGGTGCTGAAAAAGGGAG___GTTGGGGGTAGGGAGGAAACAAGATCCCAGT CCTT C METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:169824690..169824801 32194978 MeRIP-seq:(Medium) rs970302660 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4586005,Human_RBP_ID_21893876 98430 RMVar_ID_98430 Human_SNP_ID_101534138 m1A Human chr2 + 169824832 169824832 169824832 CGCCCCAGGAGACGGCGGCGGCGCACTGCTGGAGCAGCCTCAGGATCCCTCGCGCCACGACCACG CGCCCCAGGAGACGGCGGCGGCGCACTGCTGGGGCAGCCTCAGGATCCCTCGCGCCACGACCACG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr2:169824627..169824835;chr2:169824760..169824860 26863410,26863196 MeRIP-seq:(Medium) rs1343970606 Functional Loss SNV dbSNP153 33..33 33 - - - 98431 RMVar_ID_98431 Human_SNP_ID_101534152 m1A Human chr2 + 169824862 169824862 169824862 GGAGCAGCCTCAGGATCCCTCGCGCCACGACCACGCACCTCTGGAGGCGACCCGCACCTCGGCCG GGAGCAGCCTCAGGATCCCTCGCGCCACGACCGCGCACCTCTGGAGGCGACCCGCACCTCGGCCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:169824735..169824878 26863196 MeRIP-seq:(Medium) rs1180731083 Functional Loss SNV dbSNP153 33..33 33 - - - 98432 RMVar_ID_98432 Human_SNP_ID_101535052 m1A Human chr2 + 169827899 169827899 169827899 CGGCCTGGTCTGGACAGCCAACTTCGTGGCCTACCGCTGCCGGACGTGCGGCATCTCGCCCTGCA CGGCCTGGTCTGGACAGCCAACTTCGTGGCCTGCCGCTGCCGGACGTGCGGCATCTCGCCCTGCA A G UBR3 Ensembl:ENSG00000144357 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:169827852..169827963 32194978 MeRIP-seq:(Medium) rs1170168554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8851617,Human_RBP_ID_22076686 98433 RMVar_ID_98433 Human_SNP_ID_101574283 m1A Human chr2 + 169983104 169983104 169983104 TAGAGTTGAGAGAGTGAGAGCGAGAGAGAGAAACTATGCAAGGTGGAGTTGAGAGTGAGAGCAAG TAGAGTTGAGAGAGTGAGAGCGAGAGAGAGAAGCTATGCAAGGTGGAGTTGAGAGTGAGAGCAAG A G UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:169983022..169983151 26863196 MeRIP-seq:(Medium) rs1008275340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6685,RMVar_hsa_circ_44133,RMVar_hsa_circ_42639,RMVar_hsa_circ_115786,RMVar_hsa_circ_204485,RMVar_hsa_circ_30912,RMVar_hsa_circ_105610,RMVar_hsa_circ_204493,RMVar_hsa_circ_72304,RMVar_hsa_circ_43076,RMVar_hsa_circ_32938,RMVar_hsa_circ_74960,RMVar_hsa_circ_47338,RMVar_hsa_circ_71994,RMVar_hsa_circ_76615,RMVar_hsa_circ_204517,RMVar_hsa_circ_64273,RMVar_hsa_circ_114690,RMVar_hsa_circ_17532,RMVar_hsa_circ_21372,RMVar_hsa_circ_204521,RMVar_hsa_circ_284034,RMVar_hsa_circ_304107,RMVar_hsa_circ_326721,RMVar_hsa_circ_204518,RMVar_hsa_circ_361196,RMVar_hsa_circ_319225,RMVar_hsa_circ_297134,RMVar_hsa_circ_277931,RMVar_hsa_circ_24506,RMVar_hsa_circ_29434,RMVar_hsa_circ_204522,RMVar_hsa_circ_336335,RMVar_hsa_circ_204519,RMVar_hsa_circ_204520,RMVar_hsa_circ_378000,RMVar_hsa_circ_379086,RMVar_hsa_circ_325931,RMVar_hsa_circ_330386,RMVar_hsa_circ_54747,RMVar_hsa_circ_78628,RMVar_hsa_circ_360173,RMVar_hsa_circ_360556,RMVar_hsa_circ_323108,RMVar_hsa_circ_37670,RMVar_hsa_circ_61454,RMVar_hsa_circ_98398,RMVar_hsa_circ_204524,RMVar_hsa_circ_60839,RMVar_hsa_circ_204525 98434 RMVar_ID_98434 Human_SNP_ID_101751206 m1A Human chr2 + 170712973 170712973 170712973 GCATCTTGGAGAAAAAGCTAATTCCCATAACTATGGGGATGTGAAATGGCTTTTCTGGCCTTTTT GCATCTTGGAGAAAAAGCTAATTCCCATAACTGTGGGGATGTGAAATGGCTTTTCTGGCCTTTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:170712931..170713000 26863196 MeRIP-seq:(Medium) rs986704196 Functional Loss SNV dbSNP153 33..33 33 - - - 98435 RMVar_ID_98435 Human_SNP_ID_101760789 m1A Human chr2 + 170751818 170751818 170751818 GCCCACTCGAGCCGCAGCCATGTCTGGGGACGAGATGATTTTTGATCCTACTATGAGCAAGAAGA GCCCACTCGAGCCGCAGCCATGTCTGGGGACGGGATGATTTTTGATCCTACTATGAGCAAGAAGA A G EIF2S2P4 Ensembl:ENSG00000128692 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:170751732..170751819 26863410 MeRIP-seq:(Medium) rs1356535623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1579739,Human_RBP_ID_1902208,Human_RBP_ID_17394110,Human_RBP_ID_17504347 98436 RMVar_ID_98436 Human_SNP_ID_101784526 m1A Human chr2 + 170850357 170850357 170850357 TTCAGACAGGGTAGTCAGAGGCCTTCCTGAGGAGGTAACATATCAGCAGATACTGCGATAAAGGG TTCAGACAGGGTAGTCAGAGGCCTTCCTGAGGCGGTAACATATCAGCAGATACTGCGATAAAGGG A C GAD1 Ensembl:ENSG00000128683 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:170850344..170850518 26863196 MeRIP-seq:(Medium) rs1227619064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34190,RMVar_hsa_circ_204567,RMVar_hsa_circ_304492,RMVar_hsa_circ_292087 98437 RMVar_ID_98437 Human_SNP_ID_101784562 m1A Human chr2 + 170850531 170850531 170850531 CATTGGGGCTGGAGCAAGGTGAGAGAGGTAGAAGCAGACTAAGGAGGGAGAGGCAAACATGGAGC CATTGGGGCTGGAGCAAGGTGAGAGAGGTAGAGGCAGACTAAGGAGGGAGAGGCAAACATGGAGC A G GAD1 Ensembl:ENSG00000128683 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:170850369..170850563 26863196 MeRIP-seq:(Medium) rs1273960860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34190,RMVar_hsa_circ_204567,RMVar_hsa_circ_304492,RMVar_hsa_circ_292087 98438 RMVar_ID_98438 Human_SNP_ID_101802993 m1A Human chr2 - 170929316 170929316 170929316 GAGCCCATGGCGGCGGGCGATCGGTGTGGCCGAGCCGGGCTCCGCGCTGCTCCCGCCCCCAGCGC GAGCCCATGGCGGCGGGCGATCGGTGTGGCCGGGCCGGGCTCCGCGCTGCTCCCGCCCCCAGCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:170929226..170929491 26863196 MeRIP-seq:(Medium) rs1429040716 Functional Loss SNV dbSNP153 33..33 33 - - - 98439 RMVar_ID_98439 Human_SNP_ID_101811452 m1A Human chr2 + 170962900 170962900 170962900 AACCTCCCCAACCTCAACCTCAACCTCCCAGCACCACACATCATGCCAGGGGTTGGCTTACCAGA AACCTCCCCAACCTCAACCTCAACCTCCCAGCGCCACACATCATGCCAGGGGTTGGCTTACCAGA A G GORASP2 Ensembl:ENSG00000115806 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:170962876..170962900 26863196 MeRIP-seq:(Medium) rs562951993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17277991,Human_RBP_ID_17392818,Human_RBP_ID_17510157,Human_RBP_ID_18948381,Human_RBP_ID_27283945 Human_Splice_Rec_322522,Human_Splice_Rec_322523,Human_Splice_Rec_322540,Human_Splice_Rec_322541,Human_Splice_Rec_322572,Human_Splice_Rec_322573,Human_Splice_Rec_322586,Human_Splice_Rec_322587 Human_miRNA_ID_2075361,Human_miRNA_ID_2436031 RMVar_hsa_circ_345410,RMVar_hsa_circ_204572,RMVar_hsa_circ_204576,RMVar_hsa_circ_375050,RMVar_hsa_circ_89579,RMVar_hsa_circ_315783,RMVar_hsa_circ_204577,RMVar_hsa_circ_204578 98440 RMVar_ID_98440 Human_SNP_ID_101812272 m1A Human chr2 + 170965859 170965859 170965859 ACCTGGCATTGCACCTCTCCCCCTGCCATCCGAGTTCCTCCCGTCATTCCCCTTGGTTCCAGAGA ACCTGGCATTGCACCTCTCCCCCTGCCATCCGGGTTCCTCCCGTCATTCCCCTTGGTTCCAGAGA A G GORASP2 Ensembl:ENSG00000115806 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:170965776..170966075 26863196 MeRIP-seq:(Medium) rs369882237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17392822,Human_RBP_ID_17509763,Human_RBP_ID_17658190,Human_RBP_ID_18193396,Human_RBP_ID_18948383,Human_RBP_ID_22077778,Human_RBP_ID_27283949 Human_Splice_Rec_322524,Human_Splice_Rec_322542,Human_Splice_Rec_322574,Human_Splice_Rec_322588 Human_miRNA_ID_3076709 RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 98441 RMVar_ID_98441 Human_SNP_ID_101812296 m1A Human chr2 - 170965927 170965927 170965927 GTCGGAGGGTGCGTTGCTGGTGGGCGGGAGGGAAGACAGCAGCTCTCCTGAGCTTGCTGCAGAAG GTCGGAGGGTGCGTTGCTGGTGGGCGGGAGGGTAGACAGCAGCTCTCCTGAGCTTGCTGCAGAAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:170962838..170966100;chr2:170962851..170966125 26863196 MeRIP-seq:(Medium) rs1264496488 Functional Loss SNV dbSNP153 33..33 33 - - - 98442 RMVar_ID_98442 Human_SNP_ID_101812417 m1A Human chr2 - 170966180 170966180 170966180 TATGAAATTAATGATAGTTTGCGTTTCCAGACACGCTCCCGTGGTTAAATATACCACGCCAATTC TATGAAATTAATGATAGTTTGCGTTTCCAGACGCGCTCCCGTGGTTAAATATACCACGCCAATTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:170966130..170966300 32194978 MeRIP-seq:(Medium) rs992753001 Functional Loss SNV dbSNP153 33..33 33 - - - 98443 RMVar_ID_98443 Human_SNP_ID_101820637 m1A Human chr2 - 170993102 170993102 170993102 AAAGGGAGAGCTATTATTTCTAAATACTTTACACCTTTGACAAAATGAGCTGCTTGTGTTGAAAT AAAGGGAGAGCTATTATTTCTAAATACTTTACGCCTTTGACAAAATGAGCTGCTTGTGTTGAAAT T C TLK1 Ensembl:ENSG00000198586 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1045327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2601601,Human_RBP_ID_6848676,Human_RBP_ID_17277999,Human_RBP_ID_17504376,Human_RBP_ID_17943632,Human_RBP_ID_18311550 Human_miRNA_ID_448034,Human_miRNA_ID_451927 GWAS_ID_12964,GWAS_ID_12965,GWAS_ID_12966,GWAS_ID_12967,GWAS_ID_12968,GWAS_ID_12969,GWAS_ID_12970,GWAS_ID_12971,GWAS_ID_12972,GWAS_ID_12973,GWAS_ID_12974,GWAS_ID_12975,GWAS_ID_12976,GWAS_ID_12977,GWAS_ID_12978,GWAS_ID_12979,GWAS_ID_12980,GWAS_ID_12981,GWAS_ID_12982,GWAS_ID_12983,GWAS_ID_12984,GWAS_ID_12985,GWAS_ID_12986,GWAS_ID_12987,GWAS_ID_12988,GWAS_ID_12989,GWAS_ID_12990,GWAS_ID_12991,GWAS_ID_12992,GWAS_ID_12993,GWAS_ID_12994,GWAS_ID_12995,GWAS_ID_12996,GWAS_ID_12997,GWAS_ID_12998,GWAS_ID_12999,GWAS_ID_13000,GWAS_ID_13001,GWAS_ID_13002,GWAS_ID_13003,GWAS_ID_13004,GWAS_ID_13005,GWAS_ID_13006,GWAS_ID_13007,GWAS_ID_13008,GWAS_ID_13009,GWAS_ID_13010,GWAS_ID_13011,GWAS_ID_13012,GWAS_ID_13013,GWAS_ID_13014,GWAS_ID_13015,GWAS_ID_13016,GWAS_ID_13017,GWAS_ID_13018,GWAS_ID_13019,GWAS_ID_13020,GWAS_ID_13021,GWAS_ID_13022,GWAS_ID_13023,GWAS_ID_13024,GWAS_ID_13025,GWAS_ID_13026,GWAS_ID_13027,GWAS_ID_13028,GWAS_ID_13029,GWAS_ID_13030,GWAS_ID_13031,GWAS_ID_13032,GWAS_ID_13033,GWAS_ID_13034,GWAS_ID_13035,GWAS_ID_13036,GWAS_ID_13037,GWAS_ID_13038,GWAS_ID_13039,GWAS_ID_13040,GWAS_ID_13041,GWAS_ID_13042,GWAS_ID_13043,GWAS_ID_13044,GWAS_ID_13045,GWAS_ID_13046,GWAS_ID_13047,GWAS_ID_13048,GWAS_ID_13049,GWAS_ID_13050,GWAS_ID_13051,GWAS_ID_13052,GWAS_ID_13053,GWAS_ID_13054,GWAS_ID_13055,GWAS_ID_13056,GWAS_ID_13057,GWAS_ID_13058 RMVar_hsa_circ_111553,RMVar_hsa_circ_204579 98444 RMVar_ID_98444 Human_SNP_ID_101822160 m1A Human chr2 + 170998480 170998480 170998480 GCTCTCCTTTATCCTCTGAGCTCTTGAATATGACAATCACTACTGCCTTCCCTAATCACTCCAAT GCTCTCCTTTATCCTCTGAGCTCTTGAATATGGCAATCACTACTGCCTTCCCTAATCACTCCAAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:170998443..170998571 26863196 MeRIP-seq:(Medium) rs1018591464 Functional Loss SNV dbSNP153 33..33 33 - - - 98445 RMVar_ID_98445 Human_SNP_ID_101863525 m1A Human chr2 + 171159943 171159941 171159943 AGAGACCGGAGGCCAGGAGGTTAAGAGTACTGAGTGTACTGGCAAATGGAGCAGAAAGGGGCTCG AGAGACCGGAGGCCAGGAGGTTAAGAGTACT__GTGTACTGGCAAATGGAGCAGAAAGGGGCTCG TGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:171159940..171160099 26863196 MeRIP-seq:(Medium) rs1163997034 Functional Loss DEL dbSNP153 32..33 33 - - - 98446 RMVar_ID_98446 Human_SNP_ID_101863527 m1A Human chr2 + 171159943 171159943 171159943 AGAGACCGGAGGCCAGGAGGTTAAGAGTACTGAGTGTACTGGCAAATGGAGCAGAAAGGGGCTCG AGAGACCGGAGGCCAGGAGGTTAAGAGTACTGCGTGTACTGGCAAATGGAGCAGAAAGGGGCTCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:171159940..171160099 26863196 MeRIP-seq:(Medium) rs758456472 Functional Loss SNV dbSNP153 33..33 33 - - - 98447 RMVar_ID_98447 Human_SNP_ID_101863782 m1A Human chr2 - 171160418 171160418 171160418 CGGGTTCCCAGAAAGTAGCTTGATGAGTGTCCAAAGTAGCAGTGGAAGTTTGGAGGGGCCGCCAT CGGGTTCCCAGAAAGTAGCTTGATGAGTGTCCGAAGTAGCAGTGGAAGTTTGGAGGGGCCGCCAT T C TLK1 Ensembl:ENSG00000198586 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:171160367..171231165 26863196 MeRIP-seq:(Medium) rs772620114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_537627,Human_RBP_ID_1193740,Human_RBP_ID_1579797,Human_RBP_ID_3638207,Human_RBP_ID_3959672,Human_RBP_ID_5501218,Human_RBP_ID_9387660,Human_RBP_ID_17569335,Human_RBP_ID_18493626,Human_RBP_ID_23836676 Human_miRNA_ID_2967596 RMVar_hsa_circ_127131,RMVar_hsa_circ_204598,RMVar_hsa_circ_118263,RMVar_hsa_circ_204606,RMVar_hsa_circ_125471,RMVar_hsa_circ_204610 98448 RMVar_ID_98448 Human_SNP_ID_101863837 m1A Human chr2 - 171160498 171160491 171160498 GCTCGCCCTCAGCGCGGCCCCCGCCATGACGGAGGCGGGTGCCGGTGCCGTTGCCGCCGCTGCCG GCTCGCCCTCAGCGCGGCCCCCGCCATGACGG_______TGCCGGTGCCGTTGCCGCCGCTGCCG ACCCGCCT A TLK1 Ensembl:ENSG00000198586 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:171160459..171160669 26863196 MeRIP-seq:(Medium) rs1331441443 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_537628,Human_RBP_ID_3638208,Human_RBP_ID_5131662,Human_RBP_ID_9429370,Human_RBP_ID_17084675,Human_RBP_ID_17569336,Human_RBP_ID_18949673 RMVar_hsa_circ_127131,RMVar_hsa_circ_204598,RMVar_hsa_circ_118263,RMVar_hsa_circ_204606,RMVar_hsa_circ_125471,RMVar_hsa_circ_204610 98449 RMVar_ID_98449 Human_SNP_ID_101863913 m1A Human chr2 + 171160675 171160675 171160675 GGGGGAGAAGCGAGGGAGCGAGCGGGCGCGCCAGAGGAGAGGAGGAGGAAAGGAGCGCGGCGGCG GGGGGAGAAGCGAGGGAGCGAGCGGGCGCGCCGGAGGAGAGGAGGAGGAAAGGAGCGCGGCGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:171160323..171231165 26863196 MeRIP-seq:(Medium) rs769085376 Functional Loss SNV dbSNP153 33..33 33 - - - 98450 RMVar_ID_98450 Human_SNP_ID_101901492 m1A Human chr2 + 171320957 171320957 171320957 TCAGAGACTAGAAGTCATACACCTGCTAGTCTAGGTTATCTACAAGCTGACCCCCTTCCCATCTT TCAGAGACTAGAAGTCATACACCTGCTAGTCTGGGTTATCTACAAGCTGACCCCCTTCCCATCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:171320907..171321148 26863196 MeRIP-seq:(Medium) rs1559031920 Functional Loss SNV dbSNP153 33..33 33 - - - 98451 RMVar_ID_98451 Human_SNP_ID_101901524 m1A Human chr2 + 171321063 171321063 171321063 TCTTCTCACCATCTGCTGAGAATGTACATTCAAGAACTAGCCTGAGACCTACCTCCCCCAAGAAA TCTTCTCACCATCTGCTGAGAATGTACATTCATGAACTAGCCTGAGACCTACCTCCCCCAAGAAA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:171321015..171321115 26863196 MeRIP-seq:(Medium) rs1374479585 Functional Loss SNV dbSNP153 33..33 33 - - - 98452 RMVar_ID_98452 Human_SNP_ID_101939441 m1A Human chr2 - 171481479 171481476 171481480 GTCTCTCCCTGTCTTTCCTAGCCTTAACAAACAAAATTCCATACCATCCTTTAAGAACTCATCAA GTCTCTCCCTGTCTTTCCTAGCCTTAACAAA____ATTCCATACCATCCTTTAAGAACTCATCAA TTTTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:171481389..171481524 26863196 MeRIP-seq:(Medium) rs1192739098 Functional Loss DEL dbSNP153 32..35 33 - - - 98453 RMVar_ID_98453 Human_SNP_ID_101942278 m1A Human chr2 + 171492394 171492394 171492394 AGGCTAAGGCAGGAGAATCGCTTGAACCCAGAAGGCGGAGGTTGCAGTGATCTGAGATCGCACCA AGGCTAAGGCAGGAGAATCGCTTGAACCCAGAGGGCGGAGGTTGCAGTGATCTGAGATCGCACCA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:171492368..171492483 26863410 MeRIP-seq:(Medium) rs1259056062 Functional Loss SNV dbSNP153 33..33 33 - - - 98454 RMVar_ID_98454 Human_SNP_ID_101947894 m1A Human chr2 - 171517493 171517493 171517493 CAAGGCCAAGAAGGAGGCGCCGCCCATGGAGAAGCAGGAAGTGGTGAAGACGCACCTGCGGGACA CAAGGCCAAGAAGGAGGCGCCGCCCATGGAGAGGCAGGAAGTGGTGAAGACGCACCTGCGGGACA T C RPS15P4 Ensembl:ENSG00000233762 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:171517311..171517567 26863410 MeRIP-seq:(Medium) rs1218830984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1836975 98455 RMVar_ID_98455 Human_SNP_ID_101949106 m1A Human chr2 - 171522534 171522534 171522534 CCAGTAGCCCTCCATGGCCATCAGCGCCCCATACTCCGCACCGCGGGGGCCACAAGAACTTGGAG CCAGTAGCCCTCCATGGCCATCAGCGCCCCATGCTCCGCACCGCGGGGGCCACAAGAACTTGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:171522450..171522669 26863196 MeRIP-seq:(Medium) rs1420984159 Functional Loss SNV dbSNP153 33..33 33 - - - 98456 RMVar_ID_98456 Human_SNP_ID_101990918 m1A Human chr2 + 171690206 171690206 171690206 TTAAAGGCTGAGTTGGAACGTAAGAAGCAGCGACTGGCCCAAATCAGAGAGGAAAAGAAGAGAAA TTAAAGGCTGAGTTGGAACGTAAGAAGCAGCGGCTGGCCCAAATCAGAGAGGAAAAGAAGAGAAA A G DYNC1I2 Ensembl:ENSG00000077380 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:171690126..171690275 26863196 MeRIP-seq:(Medium) rs1419212812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827440,Human_RBP_ID_921595,Human_RBP_ID_17657798,Human_RBP_ID_22996892,Human_RBP_ID_23836884,Human_RBP_ID_24545912,Human_RBP_ID_26340083,Human_RBP_ID_27817772 Human_Splice_Rec_323214,Human_Splice_Rec_323215,Human_Splice_Rec_323228,Human_Splice_Rec_323229,Human_Splice_Rec_323258,Human_Splice_Rec_323259,Human_Splice_Rec_323292,Human_Splice_Rec_323293,Human_Splice_Rec_323322,Human_Splice_Rec_323323,Human_Splice_Rec_323326,Human_Splice_Rec_323327,Human_Splice_Rec_323338,Human_Splice_Rec_323339,Human_Splice_Rec_323368,Human_Splice_Rec_323369,Human_Splice_Rec_323398,Human_Splice_Rec_323399,Human_Splice_Rec_323408,Human_Splice_Rec_323409,Human_Splice_Rec_323440,Human_Splice_Rec_323441,Human_Splice_Rec_323474,Human_Splice_Rec_323475,Human_Splice_Rec_323484,Human_Splice_Rec_323485,Human_Splice_Rec_323518,Human_Splice_Rec_323519,Human_Splice_Rec_323528,Human_Splice_Rec_323529,Human_Splice_Rec_323544,Human_Splice_Rec_323545,Human_Splice_Rec_323556,Human_Splice_Rec_323557,Human_Splice_Rec_323564,Human_Splice_Rec_323565,Human_Splice_Rec_323574,Human_Splice_Rec_323575,Human_Splice_Rec_323588,Human_Splice_Rec_323589,Human_Splice_Rec_323595 Human_miRNA_ID_1337053,Human_miRNA_ID_2661223,Human_miRNA_ID_2679674 RMVar_hsa_circ_21910,RMVar_hsa_circ_101825,RMVar_hsa_circ_305993,RMVar_hsa_circ_363336,RMVar_hsa_circ_110358,RMVar_hsa_circ_30199,RMVar_hsa_circ_204649,RMVar_hsa_circ_204650 98457 RMVar_ID_98457 Human_SNP_ID_102003732 m1A Human chr2 - 171744081 171744081 171744081 GGTGACCACATAACATCATAAACATAGTCTGCATTATCTTCAAATGAATACAAAGGCTTGTTATT GGTGACCACATAACATCATAAACATAGTCTGCGTTATCTTCAAATGAATACAAAGGCTTGTTATT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:171728807..171744111 32194978 MeRIP-seq:(Medium) rs371917865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204655,RMVar_hsa_circ_204656 98458 RMVar_ID_98458 Human_SNP_ID_102039766 m1A Human chr2 + 171893929 171893929 171893929 CTGATGCCCTCCAACTCCGGACTCACAATCCCATGCACCTAGGACAGGACATTACTCTTCCTTCA CTGATGCCCTCCAACTCCGGACTCACAATCCCCTGCACCTAGGACAGGACATTACTCTTCCTTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:171893912..171893990 26863196 MeRIP-seq:(Medium) rs1192839603 Functional Loss SNV dbSNP153 33..33 33 - - - 98459 RMVar_ID_98459 Human_SNP_ID_102047726 m1A Human chr2 + 171922500 171922500 171922500 CCTTCCTCAGCCGCGGGTGATCGTAGCTCGGAAATGGCGGGTAAGTTACCGGGAAAAGTTTACCA CCTTCCTCAGCCGCGGGTGATCGTAGCTCGGAGATGGCGGGTAAGTTACCGGGAAAAGTTTACCA A G HAT1 Ensembl:ENSG00000128708 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:171922426..171922647 26863196 MeRIP-seq:(Medium) rs1361518747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623711,Human_RBP_ID_5322664,Human_RBP_ID_19102037,Human_RBP_ID_22450008 Human_Splice_Rec_323783,Human_Splice_Rec_323801,Human_Splice_Rec_323821,Human_Splice_Rec_323823 98460 RMVar_ID_98460 Human_SNP_ID_102047729 m1A Human chr2 - 171922509 171922509 171922509 TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTACCCGCCATTTCCGAGCTACGATCACCCGCGGC TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTGCCCGCCATTTCCGAGCTACGATCACCCGCGGC T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:171922465..171922560;chr2:171922426..171922647;chr2:171922479..171922581 26863196 MeRIP-seq:(Medium) rs76979357 Functional Loss SNV dbSNP153 33..33 33 - - - 98461 RMVar_ID_98461 Human_SNP_ID_102047730 m1A Human chr2 - 171922509 171922509 171922509 TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTACCCGCCATTTCCGAGCTACGATCACCCGCGGC TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTCCCCGCCATTTCCGAGCTACGATCACCCGCGGC T G SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:171922465..171922560;chr2:171922426..171922647;chr2:171922479..171922581 26863196 MeRIP-seq:(Medium) rs76979357 Functional Loss SNV dbSNP153 33..33 33 - - - 98462 RMVar_ID_98462 Human_SNP_ID_102088430 m1A Human chr2 + 172088415 172088415 172088415 TCTCCTCGGAGCCCCGCGAGGTCCGGCCCAGCAACTTCCCGGCATCCGCGCTCTAGCCTGAACCC TCTCCTCGGAGCCCCGCGAGGTCCGGCCCAGCGACTTCCCGGCATCCGCGCTCTAGCCTGAACCC A G DLX1 Ensembl:ENSG00000144355 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:172088317..172088531 26863196 MeRIP-seq:(Medium) rs1333467218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1020791,Human_RBP_ID_27475834 Human_miRNA_ID_1184309 98463 RMVar_ID_98463 Human_SNP_ID_102088457 m1A Human chr2 + 172088530 172088530 172088530 TGCCACCTGAGACAGCCCAAGCAGCAAGATAAACCCGCTCCACCCGACCCGCCGACCTTCAGCTT TGCCACCTGAGACAGCCCAAGCAGCAAGATAACCCCGCTCCACCCGACCCGCCGACCTTCAGCTT A C DLX1 Ensembl:ENSG00000144355 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:172088481..172088622 26863196 MeRIP-seq:(Medium) rs1023380288 Functional Loss SNV dbSNP153 33..33 33 - - - 98464 RMVar_ID_98464 Human_SNP_ID_102091688 m1A Human chr2 + 172100547 172100547 172100547 CTCAGTCTCTGGCGAGTTCTCCCTGGGGTTAGAAAATCGTCCCCGCGCTCACCGGGGCGCCCCCG CTCAGTCTCTGGCGAGTTCTCCCTGGGGTTAGCAAATCGTCCCCGCGCTCACCGGGGCGCCCCCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:172100521..172100660 26863196 MeRIP-seq:(Medium) rs1405733018 Functional Loss SNV dbSNP153 33..33 33 - - - 98465 RMVar_ID_98465 Human_SNP_ID_102092465 m1A Human chr2 + 172102782 172102770 172102782 TTCGGCCTCTGGGCCCGCTCGGCTCCTTGCCCAGCGCGAGCGCGGGCTCTGGCGGGGGGCGGGCA TTCGGCCTCTGGGCCCGCTCG____________GCGCGAGCGCGGGCTCTGGCGGGGGGCGGGCA GGCTCCTTGCCCA G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:172102710..172102843 26863410 MeRIP-seq:(Medium) rs1254392812 Functional Loss DEL dbSNP153 22..33 33 - - - 98466 RMVar_ID_98466 Human_SNP_ID_102092612 m1A Human chr2 - 172103119 172103119 172103119 GCTGCGGGCCACCCTGACTCCTCGCTACCTCGACCCCTCGCCTCGCTGCTCACATTCGGCGGCAG GCTGCGGGCCACCCTGACTCCTCGCTACCTCGGCCCCTCGCCTCGCTGCTCACATTCGGCGGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:172103070..172103191 26863196 MeRIP-seq:(Medium) rs193189231 Functional Loss SNV dbSNP153 33..33 33 - - - 98467 RMVar_ID_98467 Human_SNP_ID_102092613 m1A Human chr2 - 172103119 172103119 172103119 GCTGCGGGCCACCCTGACTCCTCGCTACCTCGACCCCTCGCCTCGCTGCTCACATTCGGCGGCAG GCTGCGGGCCACCCTGACTCCTCGCTACCTCGCCCCCTCGCCTCGCTGCTCACATTCGGCGGCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:172103070..172103191 26863196 MeRIP-seq:(Medium) rs193189231 Functional Loss SNV dbSNP153 33..33 33 - - - 98468 RMVar_ID_98468 Human_SNP_ID_102169934 m1A Human chr2 - 172427652 172427652 172427652 CTCTCGCCGCTGCGCCCGGCCCCACCCCCGGGACGGGTCGCGCTCTCCGTCCGGCCGCTCCCCCT CTCTCGCCGCTGCGCCCGGCCCCACCCCCGGGGCGGGTCGCGCTCTCCGTCCGGCCGCTCCCCCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:172427621..172427848;chr2:172427601..172427867 26863196 MeRIP-seq:(Medium) rs1000823821 Functional Loss SNV dbSNP153 33..33 33 - - - 98469 RMVar_ID_98469 Human_SNP_ID_102323341 m1A Human chr2 - 173075947 173075947 173075947 CAGCAGCCGGGGGCGCGGAGGCCCCGCGCGCGACGAGGGCGGCGGGGGTTGGGACGACAGCGGCC CAGCAGCCGGGGGCGCGGAGGCCCCGCGCGCGTCGAGGGCGGCGGGGGTTGGGACGACAGCGGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:173075908..173075976 26863196 MeRIP-seq:(Medium) rs1559220514 Functional Loss SNV dbSNP153 33..33 33 - - - 98470 RMVar_ID_98470 Human_SNP_ID_102330311 m1A Human chr2 - 173106760 173106760 173106760 CCTTGACCTATCATTACCTGTTCCTATACCTTATGAGTGTCACACCCTTCCCTGAAGTCTTCCCT CCTTGACCTATCATTACCTGTTCCTATACCTTGTGAGTGTCACACCCTTCCCTGAAGTCTTCCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:173106739..173106894 26863196 MeRIP-seq:(Medium) rs1276320211 Functional Loss SNV dbSNP153 33..33 33 - - - 98471 RMVar_ID_98471 Human_SNP_ID_102389646 m1A Human chr2 - 173354918 173354918 173354918 GCCCAGATCGGCGCTTGGAGCGGGGAGAGCGGAGCAGCCGCGCGGTCAGCGGTCCCACAGCAGGA GCCCAGATCGGCGCTTGGAGCGGGGAGAGCGGTGCAGCCGCGCGGTCAGCGGTCCCACAGCAGGA T A AC092573.2 Ensembl:ENSG00000236391 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:173354868..173355028 26863196 MeRIP-seq:(Medium) rs754845597 Functional Loss SNV dbSNP153 33..33 33 - - - 98472 RMVar_ID_98472 Human_SNP_ID_102389653 m1A Human chr2 - 173354925 173354925 173354925 GGCGGGTGCCCAGATCGGCGCTTGGAGCGGGGAGAGCGGAGCAGCCGCGCGGTCAGCGGTCCCAC GGCGGGTGCCCAGATCGGCGCTTGGAGCGGGGGGAGCGGAGCAGCCGCGCGGTCAGCGGTCCCAC T C AC092573.2 Ensembl:ENSG00000236391 Pseudogene intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:173354826..173358541 26863410 MeRIP-seq:(Medium) rs912954656 Functional Loss SNV dbSNP153 33..33 33 - - - 98473 RMVar_ID_98473 Human_SNP_ID_102389659 m1A Human chr2 - 173354932 173354932 173354932 TGCTGGTGGCGGGTGCCCAGATCGGCGCTTGGAGCGGGGAGAGCGGAGCAGCCGCGCGGTCAGCG TGCTGGTGGCGGGTGCCCAGATCGGCGCTTGGGGCGGGGAGAGCGGAGCAGCCGCGCGGTCAGCG T C AC092573.2 Ensembl:ENSG00000236391 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:173354883..173355019 26863196 MeRIP-seq:(Medium) rs1375383609 Functional Loss SNV dbSNP153 33..33 33 - - - 98474 RMVar_ID_98474 Human_SNP_ID_102390725 m1A Human chr2 + 173358704 173358704 173358704 TAAGCATCACGCTTAATAGGATTGCTATTTCCATTTGCAGCAGAAAGATCTCAGAGTAAAGAAGA TAAGCATCACGCTTAATAGGATTGCTATTTCCGTTTGCAGCAGAAAGATCTCAGAGTAAAGAAGA A G CDCA7 Ensembl:ENSG00000144354 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:173358701..173358725 26863196 MeRIP-seq:(Medium) rs751581799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2602433 98475 RMVar_ID_98475 Human_SNP_ID_102392655 m1A Human chr2 + 173366347 173366347 173366347 TATTGATACCAAAACAAACTGCAGAAACCCAGACTGCTGGGGCGTTCGAGGCCAGTTCTGTGGCC TATTGATACCAAAACAAACTGCAGAAACCCAGGCTGCTGGGGCGTTCGAGGCCAGTTCTGTGGCC A G CDCA7 Ensembl:ENSG00000144354 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1231312941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1579952,Human_RBP_ID_9097850,Human_RBP_ID_9385107,Human_RBP_ID_13682052,Human_RBP_ID_19000374,Human_RBP_ID_23119489,Human_RBP_ID_26820282,Human_RBP_ID_27475898 Human_Splice_Rec_325004,Human_Splice_Rec_325005,Human_Splice_Rec_325022,Human_Splice_Rec_325023,Human_Splice_Rec_325036,Human_Splice_Rec_325037,Human_Splice_Rec_325050,Human_Splice_Rec_325051,Human_Splice_Rec_325068,Human_Splice_Rec_325069 RMVar_hsa_circ_328574,RMVar_hsa_circ_39059,RMVar_hsa_circ_204731,RMVar_hsa_circ_204732 98476 RMVar_ID_98476 Human_SNP_ID_102531762 m1A Human chr2 - 173940927 173940927 173940927 AGGTTTAAGGGTTGGACACAGGAGTAGGGGTCATTATAACAGGGAAAGGGCATTGGATAGACATT AGGTTTAAGGGTTGGACACAGGAGTAGGGGTCGTTATAACAGGGAAAGGGCATTGGATAGACATT T C SP3 Ensembl:ENSG00000172845 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:173940912..173941090 26863196 MeRIP-seq:(Medium) rs1276260635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6851890,Human_RBP_ID_13682958 RMVar_hsa_circ_25580,RMVar_hsa_circ_350158,RMVar_hsa_circ_204735,RMVar_hsa_circ_204736,RMVar_hsa_circ_271251 98477 RMVar_ID_98477 Human_SNP_ID_102539326 m1A Human chr2 - 173964874 173964874 173964874 TGCGGGCGCGGGCGGGCGTGTGTGAGTGACTGACGGTGCGAGAGGAGCGAGCGCGAGTGAGAGCG TGCGGGCGCGGGCGGGCGTGTGTGAGTGACTGGCGGTGCGAGAGGAGCGAGCGCGAGTGAGAGCG T C SP3 Ensembl:ENSG00000172845 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:173964849..173964990 26863196 MeRIP-seq:(Medium) rs1436789070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_325177 98478 RMVar_ID_98478 Human_SNP_ID_102603292 m1A Human chr2 - 174248503 174248503 174248503 CTCCTTCCTCCCCGCCTCCAGCTGCCGGCAGGACCTTTCTCTCGCTGCCGCTGGGACCCCGTGTC CTCCTTCCTCCCCGCCTCCAGCTGCCGGCAGGGCCTTTCTCTCGCTGCCGCTGGGACCCCGTGTC T C OLA1 Ensembl:ENSG00000138430 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:174248407..174248550;chr2:174248402..174248557;chr2:174248392..174248550 26863196 MeRIP-seq:(Medium) rs1033796545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243345,Human_RBP_ID_4587204,Human_RBP_ID_17944336 Human_Splice_Rec_325185,Human_Splice_Rec_325205,Human_Splice_Rec_325223 98479 RMVar_ID_98479 Human_SNP_ID_102626150 m1A Human chr2 + 174337471 174337447 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGG________________________GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCGGCGGCAGCGGCGGCGGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs766194129 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_4587249 98480 RMVar_ID_98480 Human_SNP_ID_102626155 m1A Human chr2 + 174337471 174337450 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCG_____________________GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCGGCAGCGGCGGCGGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs1463664650 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_4587249 98481 RMVar_ID_98481 Human_SNP_ID_102626174 m1A Human chr2 + 174337471 174337457 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAG______________GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCGGCGGCGGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs777095000 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_4587249 98482 RMVar_ID_98482 Human_SNP_ID_102626180 m1A Human chr2 + 174337471 174337459 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCG____________GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCGGCGGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs889377194 Functional Loss DEL dbSNP153,HGVD 22..33 33 - - - Human_RBP_ID_4587249 98483 RMVar_ID_98483 Human_SNP_ID_102626183 m1A Human chr2 + 174337471 174337462 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCGGCG_________GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCGGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs754396991 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4587249 98484 RMVar_ID_98484 Human_SNP_ID_102626187 m1A Human chr2 + 174337471 174337465 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCGGCGGCG______GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCGGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs1222735319 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_4587249 98485 RMVar_ID_98485 Human_SNP_ID_102626190 m1A Human chr2 + 174337471 174337468 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCGGCGGCGGCG___GCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GGCA G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs757768733 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4587249 98486 RMVar_ID_98486 Human_SNP_ID_102626192 m1A Human chr2 + 174337471 174337471 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG A G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs368984751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4587249 98487 RMVar_ID_98487 Human_SNP_ID_102640691 m1A Human chr2 + 174395838 174395838 174395838 CTGGGAGGCCAGGTGAGGGGCGCGCACGGGGGAGGGGCGTGCATAGTTGAGACAGAAACCCGGAA CTGGGAGGCCAGGTGAGGGGCGCGCACGGGGGCGGGGCGTGCATAGTTGAGACAGAAACCCGGAA A C SCRN3 Ensembl:ENSG00000144306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:174395791..174395960 26863196 MeRIP-seq:(Medium) rs970753540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623725 98488 RMVar_ID_98488 Human_SNP_ID_102640692 m1A Human chr2 + 174395838 174395838 174395838 CTGGGAGGCCAGGTGAGGGGCGCGCACGGGGGAGGGGCGTGCATAGTTGAGACAGAAACCCGGAA CTGGGAGGCCAGGTGAGGGGCGCGCACGGGGGGGGGGCGTGCATAGTTGAGACAGAAACCCGGAA A G SCRN3 Ensembl:ENSG00000144306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:174395791..174395960 26863196 MeRIP-seq:(Medium) rs970753540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623725 98489 RMVar_ID_98489 Human_SNP_ID_102680369 m1A Human chr2 + 174567976 174567976 174567976 GGAGGAAGGGGAGGCCTGGGTCCACTCCTGGGACTGTCTACTCCACTCCTGGATGGCAACTGAGG GGAGGAAGGGGAGGCCTGGGTCCACTCCTGGGGCTGTCTACTCCACTCCTGGATGGCAACTGAGG A G AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr2:174567926..174568626;chr2:174567951..174567975 26863196 MeRIP-seq:(Medium) rs577852991 Functional Loss SNV dbSNP153 33..33 33 - - - 98490 RMVar_ID_98490 Human_SNP_ID_102681128 m1A Human chr2 - 174571819 174571819 174571819 GCCTCCTCTGCCTCCAAGTTCCAGCGGCAATGACGAAACCCCAAGACTCCCACAGCGGAATCTGT GCCTCCTCTGCCTCCAAGTTCCAGCGGCAATGGCGAAACCCCAAGACTCCCACAGCGGAATCTGT T C WIPF1 Ensembl:ENSG00000115935 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:174571706..174572240 26863196 MeRIP-seq:(Medium) rs1284391680 Functional Loss SNV dbSNP153 33..33 33 - - - 98491 RMVar_ID_98491 Human_SNP_ID_102681139 m1A Human chr2 - 174571835 174571835 174571835 CCAGCAGGCCCGGGCCGCCTCCTCTGCCTCCAAGTTCCAGCGGCAATGACGAAACCCCAAGACTC CCAGCAGGCCCGGGCCGCCTCCTCTGCCTCCATGTTCCAGCGGCAATGACGAAACCCCAAGACTC T A WIPF1 Ensembl:ENSG00000115935 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:174571658..174572244 26863196 MeRIP-seq:(Medium) rs754868175 Functional Loss SNV dbSNP153 33..33 33 - - - 98492 RMVar_ID_98492 Human_SNP_ID_102681140 m1A Human chr2 - 174571835 174571835 174571835 CCAGCAGGCCCGGGCCGCCTCCTCTGCCTCCAAGTTCCAGCGGCAATGACGAAACCCCAAGACTC CCAGCAGGCCCGGGCCGCCTCCTCTGCCTCCAGGTTCCAGCGGCAATGACGAAACCCCAAGACTC T C WIPF1 Ensembl:ENSG00000115935 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:174571658..174572244 26863196 MeRIP-seq:(Medium) rs754868175 Functional Loss SNV dbSNP153 33..33 33 - - - 98493 RMVar_ID_98493 Human_SNP_ID_102681180 m1A Human chr2 + 174571920 174571920 174571920 GCCTGTGAGGAGGCCGAAGGCCGCGGAGTGGAAGGCACTGGAGGCTTGTTGTTCTGAGGAGGAGG GCCTGTGAGGAGGCCGAAGGCCGCGGAGTGGAGGGCACTGGAGGCTTGTTGTTCTGAGGAGGAGG A G AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:174571822..174571966 26863196 MeRIP-seq:(Medium) rs887567339 Functional Loss SNV dbSNP153 33..33 33 - - - 98494 RMVar_ID_98494 Human_SNP_ID_102684087 m1A Human chr2 - 174585503 174585500 174585504 GACGTTTGCACTGGTGAGTGTCTCCTCCCCAAACACTTTCTATGCATAAAGCAAGCCAAATGAAG GACGTTTGCACTGGTGAGTGTCTCCTCCCCA____CTTTCTATGCATAAAGCAAGCCAAATGAAG GTGTT G WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:174585501..174585575 26863196 MeRIP-seq:(Medium) rs746512779 Functional Loss DEL dbSNP153 32..35 33 - - - 98495 RMVar_ID_98495 Human_SNP_ID_102692638 m1A Human chr2 - 174627435 174627434 174627435 GAGAAAGGAAGAAAGAAAGGAAAGAAAGAGAAAGGAAAGAAAGAAGGAAAGAAGAAAAGAAAAAG GAGAAAGGAAGAAAGAAAGGAAAGAAAGAGAA_GGAAAGAAAGAAGGAAAGAAGAAAAGAAAAAG CT C WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174627432..174627530 26863196 MeRIP-seq:(Medium) rs1487487014 Functional Loss DEL dbSNP153 33..33 33 - - - 98496 RMVar_ID_98496 Human_SNP_ID_102703328 m1A Human chr2 + 174676472 174676472 174676472 GGACTACAGGTGTGCACCACGACGTCCAGCTAATTTTTGTATTTTGTGTAGAGATGGGGTTTTGC GGACTACAGGTGTGCACCACGACGTCCAGCTAGTTTTTGTATTTTGTGTAGAGATGGGGTTTTGC A G AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:174676470..174676586 26863196 MeRIP-seq:(Medium) rs1284772367 Functional Loss SNV dbSNP153 33..33 33 - - - 98497 RMVar_ID_98497 Human_SNP_ID_102704753 m1A Human chr2 - 174682822 174682822 174682822 CCTGCGGACCCCGGGAGAAGTTTCCCAGAAAAAATGCCCAGCGCGGCGCGGGGCTGCGGAGTCGT CCTGCGGACCCCGGGAGAAGTTTCCCAGAAAAGATGCCCAGCGCGGCGCGGGGCTGCGGAGTCGT T C WIPF1 Ensembl:ENSG00000115935 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174677060..174683012 26863196 MeRIP-seq:(Medium) rs919859697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4628376 Human_Splice_Rec_325615,Human_Splice_Rec_325631,Human_Splice_Rec_325679,Human_Splice_Rec_325727,Human_Splice_Rec_325729 98498 RMVar_ID_98498 Human_SNP_ID_102704758 m1A Human chr2 + 174682832 174682832 174682832 AGCCCCGCGCCGCGCTGGGCATTTTTTCTGGGAAACTTCTCCCGGGGTCCGCAGGGCTGAGCCGG AGCCCCGCGCCGCGCTGGGCATTTTTTCTGGGTAACTTCTCCCGGGGTCCGCAGGGCTGAGCCGG A T AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:174682826..174682850 26863196 MeRIP-seq:(Medium) rs894496610 Functional Loss SNV dbSNP153 33..33 33 - - - 98499 RMVar_ID_98499 Human_SNP_ID_102820531 m1A Human chr2 + 175168597 175168594 175168597 GCTTTGGCGGTGTGAGGGGAGGAAAGGTGGTGAGCTCCGGAAAGGCTGCTAGAGGGAAAGCAGGA GCTTTGGCGGTGTGAGGGGAGGAAAGGTGG___GCTCCGGAAAGGCTGCTAGAGGGAAAGCAGGA GTGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:175168547..175168676 26863196 MeRIP-seq:(Medium) rs199943505 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23839037 98500 RMVar_ID_98500 Human_SNP_ID_102822853 m1A Human chr2 + 175178327 175178325 175178327 GCAAACAAAATCAAGAAAGCAACCATCAAACAAAAGAGACCCATAGCTTCAGACAAGGCAAATCC GCAAACAAAATCAAGAAAGCAACCATCAAAC__AAGAGACCCATAGCTTCAGACAAGGCAAATCC CAA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:175178276..175178425 32194978 MeRIP-seq:(Medium) rs1466461225 Functional Loss DEL dbSNP153 32..33 33 - - - 98501 RMVar_ID_98501 Human_SNP_ID_102822854 m1A Human chr2 + 175178327 175178327 175178327 GCAAACAAAATCAAGAAAGCAACCATCAAACAAAAGAGACCCATAGCTTCAGACAAGGCAAATCC GCAAACAAAATCAAGAAAGCAACCATCAAACAGAAGAGACCCATAGCTTCAGACAAGGCAAATCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:175178276..175178425 32194978 MeRIP-seq:(Medium) rs1338580288 Functional Loss SNV dbSNP153 33..33 33 - - - 98502 RMVar_ID_98502 Human_SNP_ID_102823058 m1A Human chr2 - 175179210 175179210 175179210 GGTATTTAATGGGGCCCAGAATGGTGTGTCTCAGCTAATCCAAAGGGAGTTTCAGACCAGTGCAA GGTATTTAATGGGGCCCAGAATGGTGTGTCTCCGCTAATCCAAAGGGAGTTTCAGACCAGTGCAA T G ATP5MC3 Ensembl:ENSG00000154518 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:175179128..175179296 26863196 MeRIP-seq:(Medium) rs775248526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59791,Human_RBP_ID_538588,Human_RBP_ID_920331,Human_RBP_ID_1580224,Human_RBP_ID_1903446,Human_RBP_ID_3605036,Human_RBP_ID_4587478,Human_RBP_ID_9098219,Human_RBP_ID_17658653,Human_RBP_ID_17964257,Human_RBP_ID_18749926,Human_RBP_ID_22450019,Human_RBP_ID_22765191,Human_RBP_ID_22814027,Human_RBP_ID_23212133,Human_RBP_ID_23839089,Human_RBP_ID_27003013,Human_RBP_ID_27284271 Human_Splice_Rec_326772,Human_Splice_Rec_326780,Human_Splice_Rec_326786,Human_Splice_Rec_326794 Human_miRNA_ID_2192332,Human_miRNA_ID_2206540 RMVar_hsa_circ_39420,RMVar_hsa_circ_82596,RMVar_hsa_circ_51830,RMVar_hsa_circ_204800 98503 RMVar_ID_98503 Human_SNP_ID_102823067 m1A Human chr2 - 175179234 175179234 175179234 ATTTTCTGTTTTCCAGGGCTCTACGGTATTTAATGGGGCCCAGAATGGTGTGTCTCAGCTAATCC ATTTTCTGTTTTCCAGGGCTCTACGGTATTTATTGGGGCCCAGAATGGTGTGTCTCAGCTAATCC T A ATP5MC3 Ensembl:ENSG00000154518 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:175179051..175179275 32194978 MeRIP-seq:(Medium) rs758429653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243080,Human_RBP_ID_538592,Human_RBP_ID_776312,Human_RBP_ID_920331,Human_RBP_ID_4624858,Human_RBP_ID_17658654,Human_RBP_ID_17944621,Human_RBP_ID_22450020,Human_RBP_ID_23212133 Human_Splice_Rec_326772,Human_Splice_Rec_326780,Human_Splice_Rec_326786,Human_Splice_Rec_326794 Human_miRNA_ID_2294905,Human_miRNA_ID_2428249 RMVar_hsa_circ_39420,RMVar_hsa_circ_82596,RMVar_hsa_circ_51830,RMVar_hsa_circ_204800 98504 RMVar_ID_98504 Human_SNP_ID_102823068 m1A Human chr2 - 175179234 175179234 175179234 ATTTTCTGTTTTCCAGGGCTCTACGGTATTTAATGGGGCCCAGAATGGTGTGTCTCAGCTAATCC ATTTTCTGTTTTCCAGGGCTCTACGGTATTTAGTGGGGCCCAGAATGGTGTGTCTCAGCTAATCC T C ATP5MC3 Ensembl:ENSG00000154518 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:175179051..175179275 32194978 MeRIP-seq:(Medium) rs758429653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243080,Human_RBP_ID_538592,Human_RBP_ID_776312,Human_RBP_ID_920331,Human_RBP_ID_4624858,Human_RBP_ID_17658654,Human_RBP_ID_17944621,Human_RBP_ID_22450020,Human_RBP_ID_23212133 Human_Splice_Rec_326772,Human_Splice_Rec_326780,Human_Splice_Rec_326786,Human_Splice_Rec_326794 Human_miRNA_ID_2294905,Human_miRNA_ID_2428249 RMVar_hsa_circ_39420,RMVar_hsa_circ_82596,RMVar_hsa_circ_51830,RMVar_hsa_circ_204800 98505 RMVar_ID_98505 Human_SNP_ID_102823663 m1A Human chr2 - 175181454 175181454 175181454 AAGCCTCTTTTCCTCCGCAGAGAGGAAGCGGGAGAGGAGCCCACGTCGCCTGTCACCCAATATCT AAGCCTCTTTTCCTCCGCAGAGAGGAAGCGGGCGAGGAGCCCACGTCGCCTGTCACCCAATATCT T G ATP5MC3 Ensembl:ENSG00000154518 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:175181351..175181725 26863410 MeRIP-seq:(Medium) rs940746869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243814,Human_RBP_ID_4623728,Human_RBP_ID_9330738,Human_RBP_ID_22533603 Human_Splice_Rec_326768,Human_Splice_Rec_326769,Human_Splice_Rec_326776,Human_Splice_Rec_326777,Human_Splice_Rec_326783,Human_Splice_Rec_326790,Human_Splice_Rec_326791,Human_Splice_Rec_326796,Human_Splice_Rec_326797 RMVar_hsa_circ_39420 98506 RMVar_ID_98506 Human_SNP_ID_102823666 m1A Human chr2 - 175181460 175181460 175181460 GACCTTAAGCCTCTTTTCCTCCGCAGAGAGGAAGCGGGAGAGGAGCCCACGTCGCCTGTCACCCA GACCTTAAGCCTCTTTTCCTCCGCAGAGAGGAGGCGGGAGAGGAGCCCACGTCGCCTGTCACCCA T C ATP5MC3 Ensembl:ENSG00000154518 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:175181351..175181674 26863196 MeRIP-seq:(Medium) rs753175334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243814,Human_RBP_ID_4623729,Human_RBP_ID_9330738,Human_RBP_ID_22533603 Human_Splice_Rec_326768,Human_Splice_Rec_326776,Human_Splice_Rec_326790,Human_Splice_Rec_326796 RMVar_hsa_circ_39420 98507 RMVar_ID_98507 Human_SNP_ID_102823693 m1A Human chr2 + 175181534 175181534 175181534 CCAGGGGCCTGTTCTTCCCACCCAGGCCCCGCAGGCTCCCGTGCACGCCGTCAGCTTGGGCCCCG CCAGGGGCCTGTTCTTCCCACCCAGGCCCCGCGGGCTCCCGTGCACGCCGTCAGCTTGGGCCCCG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:175181532..175181725 26863196 MeRIP-seq:(Medium) rs1204798712 Functional Loss SNV dbSNP153 33..33 33 - - - 98508 RMVar_ID_98508 Human_SNP_ID_102823744 m1A Human chr2 - 175181653 175181653 175181653 CAGCCCGTGCCGCCGCCGCCTCCTGGGAAGGTAAGTGGAGGGCACAGGGAGCCCGGCCTGGCCAG CAGCCCGTGCCGCCGCCGCCTCCTGGGAAGGTGAGTGGAGGGCACAGGGAGCCCGGCCTGGCCAG T C ATP5MC3 Ensembl:ENSG00000154518 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:175181651..175181700 26863196 MeRIP-seq:(Medium) rs1309622701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4628421,Human_RBP_ID_22450023,Human_RBP_ID_22814030,Human_RBP_ID_27003020,Human_RBP_ID_27284278 98509 RMVar_ID_98509 Human_SNP_ID_103014623 m1A Human chr2 - 176002208 176002208 176002208 TGCTCTGGAGGCAGGCTGGGCGGTGGCGGCCGAGACTGGCGGGGGTGGACGCCCGGGCCGGGCTG TGCTCTGGAGGCAGGCTGGGCGGTGGCGGCCGGGACTGGCGGGGGTGGACGCCCGGGCCGGGCTG T C LNPK Ensembl:ENSG00000144320 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176002161..176002249 26863196 MeRIP-seq:(Medium) rs1039005857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243766,Human_RBP_ID_4622766,Human_RBP_ID_9330740,Human_RBP_ID_18422405,Human_RBP_ID_18442720,Human_RBP_ID_19098428,Human_RBP_ID_22450617 Human_Splice_Rec_326817,Human_Splice_Rec_326841,Human_Splice_Rec_326865,Human_Splice_Rec_326905,Human_Splice_Rec_326915 98510 RMVar_ID_98510 Human_SNP_ID_103014683 m1A Human chr2 + 176002269 176002269 176002269 AGCAGGCAGCAGCCGCCACTGACAGAGAGACAAGCCGGGCCAACTCCTTCCCATGAAACCCCGCG AGCAGGCAGCAGCCGCCACTGACAGAGAGACAGGCCGGGCCAACTCCTTCCCATGAAACCCCGCG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:176002161..176002274 26863196 MeRIP-seq:(Medium) rs1440959836 Functional Loss SNV dbSNP153 33..33 33 - - - 98511 RMVar_ID_98511 Human_SNP_ID_103033110 m1A Human chr2 + 176080281 176080257 176080281 CCGGCGCCCCCGCCGCCGCCGCCACCACCACCACCGCCGCCGCCACCGCCACCCCGGGAACCCAG CCGGCGCCC________________________CCGCCGCCGCCACCGCCACCCCGGGAACCCAG CCCGCCGCCGCCGCCACCACCACCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:176080230..176080301 26863196 MeRIP-seq:(Medium) rs751581937 Functional Loss DEL dbSNP153 10..33 33 - - - 98512 RMVar_ID_98512 Human_SNP_ID_103033117 m1A Human chr2 + 176080281 176080260 176080281 CCGGCGCCCCCGCCGCCGCCGCCACCACCACCACCGCCGCCGCCACCGCCACCCCGGGAACCCAG CCGGCGCCCCCG_____________________CCGCCGCCGCCACCGCCACCCCGGGAACCCAG GCCGCCGCCGCCACCACCACCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:176080230..176080301 26863196 MeRIP-seq:(Medium) rs1372211341 Functional Loss DEL dbSNP153 13..33 33 - - - 98513 RMVar_ID_98513 Human_SNP_ID_103033134 m1A Human chr2 + 176080275 176080275 176080275 CCGGCCCCGGCGCCCCCGCCGCCGCCGCCACCACCACCACCGCCGCCGCCACCGCCACCCCGGGA CCGGCCCCGGCGCCCCCGCCGCCGCCGCCACCCCCACCACCGCCGCCGCCACCGCCACCCCGGGA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:176080175..176080361 26863196 MeRIP-seq:(Medium) rs997127370 Functional Loss SNV dbSNP153 33..33 33 - - - 98514 RMVar_ID_98514 Human_SNP_ID_103033138 m1A Human chr2 + 176080281 176080281 176080281 CCGGCGCCCCCGCCGCCGCCGCCACCACCACCACCGCCGCCGCCACCGCCACCCCGGGAACCCAG CCGGCGCCCCCGCCGCCGCCGCCACCACCACCGCCGCCGCCGCCACCGCCACCCCGGGAACCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:176080230..176080301 26863196 MeRIP-seq:(Medium) rs1197853839 Functional Loss SNV dbSNP153 33..33 33 - - - 98515 RMVar_ID_98515 Human_SNP_ID_103036754 m1A Human chr2 + 176092759 176092759 176092759 GGGCAGGCGGGCCGGAGGCGGGAGGCTCACAGAGGGAGAGAGGGCTAGAGGAAGAGGGCGGGAGC GGGCAGGCGGGCCGGAGGCGGGAGGCTCACAGTGGGAGAGAGGGCTAGAGGAAGAGGGCGGGAGC A T HOXD13 Ensembl:ENSG00000128714 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176092711..176092940 26863196 MeRIP-seq:(Medium) rs1232677917 Functional Loss SNV dbSNP153 33..33 33 - - - 98516 RMVar_ID_98516 Human_SNP_ID_103036762 m1A Human chr2 + 176092781 176092781 176092781 AGGCTCACAGAGGGAGAGAGGGCTAGAGGAAGAGGGCGGGAGCGAGCGAACCAGAGAGAAAGGAG AGGCTCACAGAGGGAGAGAGGGCTAGAGGAAGTGGGCGGGAGCGAGCGAACCAGAGAGAAAGGAG A T HOXD13 Ensembl:ENSG00000128714 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176092731..176092877 26863196 MeRIP-seq:(Medium) rs1400564662 Functional Loss SNV dbSNP153 33..33 33 - - - 98517 RMVar_ID_98517 Human_SNP_ID_103036790 m1A Human chr2 + 176092864 176092864 176092864 CGCGCCATGGTGTCCTGCGCGGGGCCAGGGCCAGGGCCGGGGCCGGGCCAGGCCGGGCCATGAGC CGCGCCATGGTGTCCTGCGCGGGGCCAGGGCCGGGGCCGGGGCCGGGCCAGGCCGGGCCATGAGC A G HOXD13 Ensembl:ENSG00000128714 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:176092767..176092910 26863196 MeRIP-seq:(Medium) rs1019653707 Functional Loss SNV dbSNP153 33..33 33 - - - 98518 RMVar_ID_98518 Human_SNP_ID_103036885 m1A Human chr2 + 176093073 176093052 176093073 GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCAGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGACGCATTCG_____________________GCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGGCGGGCGGCGGCGGCGGCA G HOXD13 Ensembl:ENSG00000128714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:176092976..176093200 26863410 MeRIP-seq:(Medium) rs587776824 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_538755 Clinvar_Rec_598 98519 RMVar_ID_98519 Human_SNP_ID_103036917 m1A Human chr2 + 176093073 176093064 176093073 GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCAGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGACGCATTCGGGGCGGGCGGCG_________GCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGCGGCGGCA G HOXD13 Ensembl:ENSG00000128714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:176092976..176093200 26863410 MeRIP-seq:(Medium) rs749930395 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_538755 98520 RMVar_ID_98520 Human_SNP_ID_103036928 m1A Human chr2 + 176093073 176093073 176093073 GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCAGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCGGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC A G HOXD13 Ensembl:ENSG00000128714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:176092976..176093200 26863410 MeRIP-seq:(Medium) rs540457957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_538755 98521 RMVar_ID_98521 Human_SNP_ID_103036929 m1A Human chr2 + 176093073 176093073 176093073 GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCAGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCTGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC A T HOXD13 Ensembl:ENSG00000128714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:176092976..176093200 26863410 MeRIP-seq:(Medium) rs540457957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_538755 98522 RMVar_ID_98522 Human_SNP_ID_103041394 m1A Human chr2 + 176107009 176107009 176107009 TTCGGGCGGTGGCAGATGCGCCCAGCGGTGACAGCGGCCAGCGGCGCGCAGGTGACCGGCCTGAG TTCGGGCGGTGGCAGATGCGCCCAGCGGTGACGGCGGCCAGCGGCGCGCAGGTGACCGGCCTGAG A G HOXD11 Ensembl:ENSG00000128713 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176106964..176107272 26863196 MeRIP-seq:(Medium) rs1394180222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4587747 98523 RMVar_ID_98523 Human_SNP_ID_103041669 m1A Human chr2 - 176107578 176107578 176107578 CCCCGCGCTGCCGCCGCCGCCGCCGCCGCGGTACGGCCACTTGGCGCGCTCCAGGCCGTAGTCGC CCCCGCGCTGCCGCCGCCGCCGCCGCCGCGGTGCGGCCACTTGGCGCGCTCCAGGCCGTAGTCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:176107528..176107650 26863196 MeRIP-seq:(Medium) rs770349959 Functional Loss SNV dbSNP153 33..33 33 - - - 98524 RMVar_ID_98524 Human_SNP_ID_103046502 m1A Human chr2 - 176122384 176122363 176122384 CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGAGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCG_____________________CCGCGGGGGCGC GCCGCTCCGTGTGCCCTGGACT G HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122336..176122468 26863196 MeRIP-seq:(Medium) rs1250131342 Functional Loss DEL dbSNP153 33..53 33 - - - Human_Splice_Rec_326956 98525 RMVar_ID_98525 Human_SNP_ID_103046510 m1A Human chr2 - 176122384 176122384 176122384 CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGAGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGTGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC T A HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122336..176122468 26863196 MeRIP-seq:(Medium) rs711820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_326956 98526 RMVar_ID_98526 Human_SNP_ID_103046511 m1A Human chr2 - 176122384 176122384 176122384 CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGAGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGGGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122336..176122468 26863196 MeRIP-seq:(Medium) rs711820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_326956 98527 RMVar_ID_98527 Human_SNP_ID_103046512 m1A Human chr2 - 176122384 176122384 176122384 CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGAGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC CTGACTCTCCAGCTTCCGAGCCGCGGGCGGCGCGTCCAGGGCACACGGAGCGGCCGCGGGGGCGC T G HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122336..176122468 26863196 MeRIP-seq:(Medium) rs711820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_326956 98528 RMVar_ID_98528 Human_SNP_ID_103046689 m1A Human chr2 + 176122763 176122763 176122763 GGGCGCCGGCGGGGAGCTGCTCGGCGGCGGACAGTGTAATGTTGGGTGGGAGTGCGGGACGCCTC GGGCGCCGGCGGGGAGCTGCTCGGCGGCGGACCGTGTAATGTTGGGTGGGAGTGCGGGACGCCTC A C HOXD9 Ensembl:ENSG00000128709 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122713..176122878 26863196 MeRIP-seq:(Medium) rs1159217663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243621,Human_RBP_ID_1193938,Human_RBP_ID_6855387,Human_RBP_ID_13692917 98529 RMVar_ID_98529 Human_SNP_ID_103046700 m1A Human chr2 - 176122783 176122783 176122783 GTGCCACTGGAAGACATTTTGAGGCGTCCCGCACTCCCACCCAACATTACACTGTCCGCCGCCGA GTGCCACTGGAAGACATTTTGAGGCGTCCCGCGCTCCCACCCAACATTACACTGTCCGCCGCCGA T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176122732..176122849 26863196 MeRIP-seq:(Medium) rs372918813 Functional Loss SNV dbSNP153 33..33 33 - - - 98530 RMVar_ID_98530 Human_SNP_ID_103047143 m1A Human chr2 + 176123565 176123562 176123565 GAAGGAGGAGGAGAAGCAGCATTCGCAGCCGCAGCAGCAGCAACTTGACCCAAGTAAGTGCAAAA GAAGGAGGAGGAGAAGCAGCATTCGCAGCC___GCAGCAGCAACTTGACCCAAGTAAGTGCAAAA CGCA C HOXD9 Ensembl:ENSG00000128709 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:176123391..176123953 26863196 MeRIP-seq:(Medium) rs56007470 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_326965 98531 RMVar_ID_98531 Human_SNP_ID_103049209 m1A Human chr2 + 176130030 176130030 176130030 AGCGGGGCAGGTCGCCTGGGGCGTCGGCGATTATATTGCGGCCGAGCCGGGGCGCGCCGGGAAAG AGCGGGGCAGGTCGCCTGGGGCGTCGGCGATTGTATTGCGGCCGAGCCGGGGCGCGCCGGGAAAG A G HOXD8 Ensembl:ENSG00000175879 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176129891..176130487 26863196 MeRIP-seq:(Medium) rs1409856452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17944791 98532 RMVar_ID_98532 Human_SNP_ID_103049587 m1A Human chr2 - 176130675 176130675 176130675 TGCGGAGGAGGAGGGGGGGCGGCCTGGTAGGCAGCGGCCGGGCTGCCCCCGCCGGGGTGGAAGTA TGCGGAGGAGGAGGGGGGGCGGCCTGGTAGGCGGCGGCCGGGCTGCCCCCGCCGGGGTGGAAGTA T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176130625..176130834 26863196 MeRIP-seq:(Medium) rs765554732 Functional Loss SNV dbSNP153 33..33 33 - - - 98533 RMVar_ID_98533 Human_SNP_ID_103049588 m1A Human chr2 - 176130675 176130675 176130675 TGCGGAGGAGGAGGGGGGGCGGCCTGGTAGGCAGCGGCCGGGCTGCCCCCGCCGGGGTGGAAGTA TGCGGAGGAGGAGGGGGGGCGGCCTGGTAGGCCGCGGCCGGGCTGCCCCCGCCGGGGTGGAAGTA T G HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176130625..176130834 26863196 MeRIP-seq:(Medium) rs765554732 Functional Loss SNV dbSNP153 33..33 33 - - - 98534 RMVar_ID_98534 Human_SNP_ID_103049644 m1A Human chr2 - 176130729 176130729 176130729 TCCCCGTGACAGGCAATCCCGCCGCAGGGGGGAGGTGGCGGCGGAGGCGGAGGATGCGGAGGAGG TCCCCGTGACAGGCAATCCCGCCGCAGGGGGGGGGTGGCGGCGGAGGCGGAGGATGCGGAGGAGG T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:176130536..176130735 32194978 MeRIP-seq:(Medium) rs1161695621 Functional Loss SNV dbSNP153 33..33 33 - - - 98535 RMVar_ID_98535 Human_SNP_ID_103051350 m1A Human chr2 - 176136707 176136707 176136707 GCGATGCGGACCGAGTGAGCGGCGGTGGGGCCAGGCCGGGCGCCGGGCGGGAGCCGAGGCCGCGG GCGATGCGGACCGAGTGAGCGGCGGTGGGGCCTGGCCGGGCGCCGGGCGGGAGCCGAGGCCGCGG T A HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr2:176135407..176136753;chr2:176135357..176137009 26863410,26863196 MeRIP-seq:(Medium) rs913522569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_326953,Human_Splice_Rec_326957,Human_Splice_Rec_326961 98536 RMVar_ID_98536 Human_SNP_ID_103051386 m1A Human chr2 - 176136805 176136805 176136805 CTCCTGGCAGGCGGTGTCGGCGCCGGCGGGGGACTCGGCGCCCAGGGCCCCTTCCAGGCCCTCCC CTCCTGGCAGGCGGTGTCGGCGCCGGCGGGGGGCTCGGCGCCCAGGGCCCCTTCCAGGCCCTCCC T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:176136761..176136901 26863196 MeRIP-seq:(Medium) rs923526328 Functional Loss SNV dbSNP153 33..33 33 - - - 98537 RMVar_ID_98537 Human_SNP_ID_103055270 m1A Human chr2 + 176152373 176152373 176152373 TTGAGGGTTCCGGACCTGGTGGTGGGCCCAGAAGAAGGAGCACATTTGGGGATCCCGCAAGCCTG TTGAGGGTTCCGGACCTGGTGGTGGGCCCAGAGGAAGGAGCACATTTGGGGATCCCGCAAGCCTG A G HOXD3,HOXD4 Ensembl:ENSG00000128652,Ensembl:ENSG00000170166 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:176152323..176152407 26863196 MeRIP-seq:(Medium) rs780642767 Functional Loss SNV dbSNP153 33..33 33 - - - 98538 RMVar_ID_98538 Human_SNP_ID_103062009 m1A Human chr2 + 176178561 176178561 176178561 ACCTGAGCCCGGCGCCTGCTGGGGAGCTGCGCAGCCAGGACAGCGGTCGGCAGCACAGGGCCTGG ACCTGAGCCCGGCGCCTGCTGGGGAGCTGCGCGGCCAGGACAGCGGTCGGCAGCACAGGGCCTGG A G HAGLROS Ensembl:ENSG00000226363 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176178512..176178603 26863196 MeRIP-seq:(Medium) rs545090864 Functional Loss SNV dbSNP153 33..33 33 - - - 98539 RMVar_ID_98539 Human_SNP_ID_103067546 m1A Human chr2 - 176200870 176200870 176200870 TTTTATAACGTGTTCAATAAAAAGCTGAACTTAAAAAAAAAAAGAAGTAACCATCATTAATATTA TTTTATAACGTGTTCAATAAAAAGCTGAACTTTAAAAAAAAAAGAAGTAACCATCATTAATATTA T A - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878996273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22998264,Human_RBP_ID_26478248 98540 RMVar_ID_98540 Human_SNP_ID_103067622 m1A Human chr2 - 176201133 176201133 176201133 GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAACCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAGCCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs563303838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064025,Human_RBP_ID_5275510,Human_RBP_ID_18750240,Human_RBP_ID_26488082 98541 RMVar_ID_98541 Human_SNP_ID_103084335 m1A Human chr2 + 176269502 176269502 176269502 GGGGGCCTCACTGCAGCCGCCGCTGCTGTTGGAGTGGGCTTTGCGAGTCTGAACGTTGGCGGGGC GGGGGCCTCACTGCAGCCGCCGCTGCTGTTGGGGTGGGCTTTGCGAGTCTGAACGTTGGCGGGGC A G MTX2 Ensembl:ENSG00000128654 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176269451..176269590 26863196 MeRIP-seq:(Medium) rs1341976546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1580506,Human_RBP_ID_4623734,Human_RBP_ID_5470230,Human_RBP_ID_18421946,Human_RBP_ID_23839601 98542 RMVar_ID_98542 Human_SNP_ID_103305251 m1A Human chr2 + 177212870 177212870 177212870 CTCCGGCCGTCGCCGTCGCCGCCGGGGGGAGGAGGTATTAGGGGGAGAGCGGGGGGTTGGTGGGG CTCCGGCCGTCGCCGTCGCCGCCGGGGGGAGGGGGTATTAGGGGGAGAGCGGGGGGTTGGTGGGG A G HNRNPA3 Ensembl:ENSG00000170144 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:177212726..177215752 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4623738,Human_RBP_ID_6856158,Human_RBP_ID_18421947 Human_Splice_Rec_327403,Human_Splice_Rec_327443 98543 RMVar_ID_98543 Human_SNP_ID_103305252 m1A Human chr2 + 177212870 177212870 177212870 CTCCGGCCGTCGCCGTCGCCGCCGGGGGGAGGAGGTATTAGGGGGAGAGCGGGGGGTTGGTGGGG CTCCGGCCGTCGCCGTCGCCGCCGGGGGGAGGTGGTATTAGGGGGAGAGCGGGGGGTTGGTGGGG A T HNRNPA3 Ensembl:ENSG00000170144 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:177212726..177215752 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4623738,Human_RBP_ID_6856158,Human_RBP_ID_18421947 Human_Splice_Rec_327403,Human_Splice_Rec_327443 98544 RMVar_ID_98544 Human_SNP_ID_103305275 m1A Human chr2 - 177212914 177212914 177212914 GGCCTCCCCGCTCCCACCGAACCAGGCCCCCAACGCCGGCCATTCCCCACCAACCCCCCGCTCTC GGCCTCCCCGCTCCCACCGAACCAGGCCCCCAGCGCCGGCCATTCCCCACCAACCCCCCGCTCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:177212861..177213029 26863196 MeRIP-seq:(Medium) rs980703844 Functional Loss SNV dbSNP153 33..33 33 - - - 98545 RMVar_ID_98545 Human_SNP_ID_103306810 m1A Human chr2 - 177216942 177216939 177216943 AAATATCAAACATCAATGAAAATAAGCCACCTACCATCACCTCCAAATCCATTATATCCACCATC AAATATCAAACATCAATGAAAATAAGCCACC____ATCACCTCCAAATCCATTATATCCACCATC TGGTA T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:177216762..177216981 26863410 MeRIP-seq:(Medium) rs1283424863 Functional Loss DEL dbSNP153 32..35 33 - - - 98546 RMVar_ID_98546 Human_SNP_ID_103307078 m1A Human chr2 - 177217721 177217721 177217721 CCATAGCCCCCTCTACTACTATAACCAGGACCACCGCCATAGTTGCCACCTAAAAAAACAACAAA CCATAGCCCCCTCTACTACTATAACCAGGACCGCCGCCATAGTTGCCACCTAAAAAAACAACAAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:177217701..177217775 26863196 MeRIP-seq:(Medium) rs1453755273 Functional Loss SNV dbSNP153 33..33 33 - - - 98547 RMVar_ID_98547 Human_SNP_ID_103307079 m1A Human chr2 - 177217721 177217721 177217721 CCATAGCCCCCTCTACTACTATAACCAGGACCACCGCCATAGTTGCCACCTAAAAAAACAACAAA CCATAGCCCCCTCTACTACTATAACCAGGACCCCCGCCATAGTTGCCACCTAAAAAAACAACAAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr2:177217701..177217775 26863196 MeRIP-seq:(Medium) rs1453755273 Functional Loss SNV dbSNP153 33..33 33 - - - 98548 RMVar_ID_98548 Human_SNP_ID_103307702 m1A Human chr2 - 177219316 177219316 177219316 TTTATCATCATAATAAAAATTTAAAGATACCTACCCTTTTCTGCTGTTTTTAGAACCTTCTGCTA TTTATCATCATAATAAAAATTTAAAGATACCTTCCCTTTTCTGCTGTTTTTAGAACCTTCTGCTA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr2:177219182..177219401;chr2:177219276..177219325 26863410,26863196 MeRIP-seq:(Medium) rs1027422327 Functional Loss SNV dbSNP153 33..33 33 - - - 98549 RMVar_ID_98549 Human_SNP_ID_103311325 m1A Human chr2 - 177231391 177231391 177231391 AAAACACCAGTACATTCTTCTGGGGATATGGTACAACCCTTGTCACCATCTCAGGGGCAGAGCAC AAAACACCAGTACATTCTTCTGGGGATATGGTGCAACCCTTGTCACCATCTCAGGGGCAGAGCAC T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:177231341..177231421 32194978 MeRIP-seq:(Medium) rs1346762075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9385117,Human_RBP_ID_17274339,Human_RBP_ID_17944991,Human_RBP_ID_22078294,Human_RBP_ID_26819080,Human_RBP_ID_27476143,Human_RBP_ID_27819160 98550 RMVar_ID_98550 Human_SNP_ID_103318958 m1A Human chr2 - 177263690 177263690 177263690 GGGCAGTGGACTCTGAGGCCGGAGTCGGCGGCACCCGGGGCTTCTAGTTCGGACGCGGTGCCCCC GGGCAGTGGACTCTGAGGCCGGAGTCGGCGGCGCCCGGGGCTTCTAGTTCGGACGCGGTGCCCCC T C NFE2L2 Ensembl:ENSG00000116044 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:177263684..177263773 26863196 MeRIP-seq:(Medium) rs1351465269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638224,Human_RBP_ID_5471466,Human_RBP_ID_5651642,Human_RBP_ID_8728555,Human_RBP_ID_17135990,Human_RBP_ID_18493647 RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 98551 RMVar_ID_98551 Human_SNP_ID_103319310 m1A Human chr2 - 177264657 177264657 177264657 GCAGCCGCCACCGCCGCCGCCGCCGCCACCAGAGCCGCCCTGTCCGCGCCGCGCCTCGGCAGCCG GCAGCCGCCACCGCCGCCGCCGCCGCCACCAGCGCCGCCCTGTCCGCGCCGCGCCTCGGCAGCCG T G NFE2L2 Ensembl:ENSG00000116044 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr2:177264576..177264725;chr2:177264551..177264693 26863410 MeRIP-seq:(Medium) rs1034286727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623740,Human_RBP_ID_8852140,Human_RBP_ID_9296858,Human_RBP_ID_9330744,Human_RBP_ID_17392843,Human_RBP_ID_18421948,Human_RBP_ID_22533548,Human_RBP_ID_22997211 98552 RMVar_ID_98552 Human_SNP_ID_103319328 m1A Human chr2 - 177264680 177264671 177264680 GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCCACCGCCGCCGCCGCCGCCACCAGAGCCGCCCTG GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCC_________GCCGCCGCCACCAGAGCCGCCCTG CGGCGGCGGT C NFE2L2 Ensembl:ENSG00000116044 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:177264526..177264725;chr2:177264501..177264700;chr2:177264170..177264799;chr2:177264201..177264775;chr2:177264192..177264752 26863196 MeRIP-seq:(Medium) rs1192556728 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_4624879,Human_RBP_ID_8852140,Human_RBP_ID_9330744,Human_RBP_ID_17392843,Human_RBP_ID_18421948,Human_RBP_ID_22533605,Human_RBP_ID_22721553,Human_RBP_ID_22997211 98553 RMVar_ID_98553 Human_SNP_ID_103319334 m1A Human chr2 - 177264680 177264677 177264680 GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCCACCGCCGCCGCCGCCGCCACCAGAGCCGCCCTG GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCC___GCCGCCGCCGCCGCCACCAGAGCCGCCCTG CGGT C NFE2L2 Ensembl:ENSG00000116044 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:177264526..177264725;chr2:177264501..177264700;chr2:177264170..177264799;chr2:177264201..177264775;chr2:177264192..177264752 26863196 MeRIP-seq:(Medium) rs1277621991 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4624879,Human_RBP_ID_8852140,Human_RBP_ID_9330744,Human_RBP_ID_17392843,Human_RBP_ID_18421948,Human_RBP_ID_22533605,Human_RBP_ID_22721553,Human_RBP_ID_22997211 98554 RMVar_ID_98554 Human_SNP_ID_103319337 m1A Human chr2 - 177264680 177264680 177264680 GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCCACCGCCGCCGCCGCCGCCACCAGAGCCGCCCTG GGGAGCCCGGAGGAGCCGCCGACGCAGCCGCCGCCGCCGCCGCCGCCGCCACCAGAGCCGCCCTG T C NFE2L2 Ensembl:ENSG00000116044 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:177264526..177264725;chr2:177264501..177264700;chr2:177264170..177264799;chr2:177264201..177264775;chr2:177264192..177264752 26863196 MeRIP-seq:(Medium) rs1178294377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4624879,Human_RBP_ID_8852140,Human_RBP_ID_9330744,Human_RBP_ID_17392843,Human_RBP_ID_18421948,Human_RBP_ID_22533605,Human_RBP_ID_22721553,Human_RBP_ID_22997211 98555 RMVar_ID_98555 Human_SNP_ID_103322115 m1A Human chr2 + 177276850 177276850 177276850 GGCCAGGCTGGTCTCCATCTTCTGACCTCGTGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGA GGCCAGGCTGGTCTCCATCTTCTGACCTCGTGGTTCACCCACCTCGGCCTCCCAAAGTGCTGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:177276746..177276869 26863196 MeRIP-seq:(Medium) rs1042513335 Functional Loss SNV dbSNP153 33..33 33 - - - 98556 RMVar_ID_98556 Human_SNP_ID_103330629 m1A Human chr2 - 177313338 177313335 177313338 AGGAAGGAAGGAAGGAGAAGAGAAAGAAAAGGAAGGAAGGAAGGAAGGAGAAAGAGAAAGAAGGA AGGAAGGAAGGAAGGAGAAGAGAAAGAAAAGG___GAAGGAAGGAAGGAGAAAGAGAAAGAAGGA CCTT C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:177313298..177313428 26863196 MeRIP-seq:(Medium) rs1350257033 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_25583212 98557 RMVar_ID_98557 Human_SNP_ID_103342611 m1A Human chr2 - 177363764 177363764 177363764 TGAAAAGACAGCGAGGAGGGGAGGTAAATCACAGTGAGGTGGAATTAGCCACAGACAGAAAGAGG TGAAAAGACAGCGAGGAGGGGAGGTAAATCACTGTGAGGTGGAATTAGCCACAGACAGAAAGAGG T A NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:177363734..177364156 26863196 MeRIP-seq:(Medium) rs79387027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827866 98558 RMVar_ID_98558 Human_SNP_ID_103348934 m1A Human chr2 - 177392826 177392826 177392826 CGCTGCAGACCCGTAGCTCGCGCCCGCGCCCAAGCCAGTCCCACCCGCTGCAGCCGCCGCCTCCG CGCTGCAGACCCGTAGCTCGCGCCCGCGCCCATGCCAGTCCCACCCGCTGCAGCCGCCGCCTCCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:177392751..177393214 26863196 MeRIP-seq:(Medium) rs1400544926 Functional Loss SNV dbSNP153 33..33 33 - - - 98559 RMVar_ID_98559 Human_SNP_ID_103348973 m1A Human chr2 + 177392872 177392872 177392872 GAGCTACGGGTCTGCAGCGGACCGGGACCGGGACCCGGACCCGGACCGCGCCGGGCGGAGGCTGC GAGCTACGGGTCTGCAGCGGACCGGGACCGGGTCCCGGACCCGGACCGCGCCGGGCGGAGGCTGC A T AGPS Ensembl:ENSG00000018510 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:177392781..177392872 26863410 MeRIP-seq:(Medium) rs764286061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243360,Human_RBP_ID_4623742,Human_RBP_ID_5528738,Human_RBP_ID_8852141,Human_RBP_ID_9296859,Human_RBP_ID_9330745,Human_RBP_ID_18421950,Human_RBP_ID_22076713,Human_RBP_ID_22450618,Human_RBP_ID_26770212 Clinvar_Rec_599 98560 RMVar_ID_98560 Human_SNP_ID_103349014 m1A Human chr2 + 177392952 177392952 177392952 ATCTGCTGGGCCGGCCCCGGGAGGCTCTGAGTACCAATGAGTGCAAAGCGCGGAGAGCCGCGTCG ATCTGCTGGGCCGGCCCCGGGAGGCTCTGAGTGCCAATGAGTGCAAAGCGCGGAGAGCCGCGTCG A G AGPS Ensembl:ENSG00000018510 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr2:177392751..177434331;chr2:177392901..177393025 26863196,32194978 MeRIP-seq:(Medium) rs1196082219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4588417,Human_RBP_ID_9330745,Human_RBP_ID_22450618,Human_RBP_ID_26341589,Human_RBP_ID_26770212 Human_Splice_Rec_327623,Human_Splice_Rec_327661 Human_miRNA_ID_1508385 98561 RMVar_ID_98561 Human_SNP_ID_103355130 m1A Human chr2 - 177420203 177420203 177420203 ATGCTAAACATCTTAAAACTGTACAGTATATCATTGATTATTAACTCACAATCATCTAAAATACC ATGCTAAACATCTTAAAACTGTACAGTATATCGTTGATTATTAACTCACAATCATCTAAAATACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:177420200..177420375 26863196 MeRIP-seq:(Medium) rs1163178241 Functional Loss SNV dbSNP153 33..33 33 - - - 98562 RMVar_ID_98562 Human_SNP_ID_103543763 m1A Human chr2 - 178226332 178226332 178226332 CCCACTGCACCACCAGCATGGAAGGTGACTGCACCACCCAGCATCCTTTGCCCACTGTGCTACCA CCCACTGCACCACCAGCATGGAAGGTGACTGCCCCACCCAGCATCCTTTGCCCACTGTGCTACCA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:178226201..178226409 26863196 MeRIP-seq:(Medium) rs1331580830 Functional Loss SNV dbSNP153 33..33 33 - - - 98563 RMVar_ID_98563 Human_SNP_ID_103595439 m1A Human chr2 + 178450411 178450411 178450411 TTCCCTGGCTTAGCTGTTATCATCTTCCCCAAACTGCAAAAACCACAAAAAGGTGTGCTTTGCAT TTCCCTGGCTTAGCTGTTATCATCTTCCCCAACCTGCAAAAACCACAAAAAGGTGTGCTTTGCAT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:178450365..178450465 26863410 MeRIP-seq:(Medium) rs777378640 Functional Loss SNV dbSNP153 33..33 33 - - - 98564 RMVar_ID_98564 Human_SNP_ID_103595440 m1A Human chr2 + 178450411 178450411 178450411 TTCCCTGGCTTAGCTGTTATCATCTTCCCCAAACTGCAAAAACCACAAAAAGGTGTGCTTTGCAT TTCCCTGGCTTAGCTGTTATCATCTTCCCCAAGCTGCAAAAACCACAAAAAGGTGTGCTTTGCAT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:178450365..178450465 26863410 MeRIP-seq:(Medium) rs777378640 Functional Loss SNV dbSNP153 33..33 33 - - - 98565 RMVar_ID_98565 Human_SNP_ID_103595479 m1A Human chr2 + 178450467 178450467 178450467 GCTTTGCATGCCAAATTGGAGATTGAAGCAGAAGCGTAGAGGCCAGTTTTAACCGCCACCGACGG GCTTTGCATGCCAAATTGGAGATTGAAGCAGAGGCGTAGAGGCCAGTTTTAACCGCCACCGACGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:178450464..178450665 26863196 MeRIP-seq:(Medium) rs1354453933 Functional Loss SNV dbSNP153 33..33 33 - - - 98566 RMVar_ID_98566 Human_SNP_ID_103595509 m1A Human chr2 - 178450563 178450563 178450563 GCGGAGTGACTGCCGCAGCGGGGCCGGAAGACAGGTGCGCCCCAGCCTCGCCAGCTCTGGCCCTG GCGGAGTGACTGCCGCAGCGGGGCCGGAAGACGGGTGCGCCCCAGCCTCGCCAGCTCTGGCCCTG T C PRKRA Ensembl:ENSG00000180228 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:178450559..178450685 26863196 MeRIP-seq:(Medium) rs578077376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_328509,Human_Splice_Rec_328561 98567 RMVar_ID_98567 Human_SNP_ID_103595740 m1A Human chr2 - 178451023 178451023 178451023 AGCCGCTGAGCCGTCCCTTCTCGCCATGTCCCAGAGCAGGCACCGCGCCGAGGCCCCGCCGCTGG AGCCGCTGAGCCGTCCCTTCTCGCCATGTCCCCGAGCAGGCACCGCGCCGAGGCCCCGCCGCTGG T G PRKRA Ensembl:ENSG00000180228 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:178450913..178451164 26863196 MeRIP-seq:(Medium) rs749472486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4588701,Human_RBP_ID_5239894,Human_RBP_ID_9330746,Human_RBP_ID_18421951 Human_Splice_Rec_328473,Human_Splice_Rec_328493,Human_Splice_Rec_328555,Human_Splice_Rec_328567,Human_Splice_Rec_328571 Human_miRNA_ID_2017616,Human_miRNA_ID_2423297,Human_miRNA_ID_2432957,Human_miRNA_ID_2906456,Human_miRNA_ID_3025287 RMVar_hsa_circ_204883,RMVar_hsa_circ_94789 98568 RMVar_ID_98568 Human_SNP_ID_103595803 m1A Human chr2 - 178451117 178451117 178451117 GGCGGGGGAGTCGGAGGAGGTGGCGGCGCTGGAGCTCCTCCCGGGGACCAGCGACCCGGGGAGCG GGCGGGGGAGTCGGAGGAGGTGGCGGCGCTGGGGCTCCTCCCGGGGACCAGCGACCCGGGGAGCG T C PRKRA Ensembl:ENSG00000180228 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:178450951..178451150 26863196 MeRIP-seq:(Medium) rs972184668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243199,Human_RBP_ID_4622769,Human_RBP_ID_5146670,Human_RBP_ID_18421952 Human_miRNA_ID_2291179,Human_miRNA_ID_2356524,Human_miRNA_ID_3058969 RMVar_hsa_circ_204883,RMVar_hsa_circ_94789 98569 RMVar_ID_98569 Human_SNP_ID_103603174 m1A Human chr2 - 178480569 178480569 178480569 GCCCGCGACCGGCCTCCTGCTCGCGCTTCCGCAGCCCGGCTGCTCCCTCCGGCGCCCCGGCGCTG GCCCGCGACCGGCCTCCTGCTCGCGCTTCCGCGGCCCGGCTGCTCCCTCCGGCGCCCCGGCGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:178480479..178480714;chr2:178480471..178480713;chr2:178480475..178480768 26863196 MeRIP-seq:(Medium) rs549429988 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_600,Clinvar_Rec_601,Clinvar_Rec_602 98570 RMVar_ID_98570 Human_SNP_ID_103816619 m1A Human chr2 + 179264577 179264577 179264577 AAGACAGGGGAACGCTAGCGAGGTGCGGGCGGAGGCGGAGGGCGCGGCGGGAGGAAGGCGGGCTG AAGACAGGGGAACGCTAGCGAGGTGCGGGCGGCGGCGGAGGGCGCGGCGGGAGGAAGGCGGGCTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:179264531..179264757 26863196 MeRIP-seq:(Medium) rs1208236359 Functional Loss SNV dbSNP153 33..33 33 - - - 98571 RMVar_ID_98571 Human_SNP_ID_103816650 m1A Human chr2 + 179264642 179264630 179264642 GGGGCGGAGCGGGCCCGGGCGGCGGCGGCAGCAGCGGCGACGGCTGCGGCTCCAGTCACTCGCGG GGGGCGGAGCGGGCCCGGGCG____________GCGGCGACGGCTGCGGCTCCAGTCACTCGCGG GGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr2:179264458..179264718;chr2:179264551..179264675 26863196,26863410 MeRIP-seq:(Medium) rs1245297617 Functional Loss DEL dbSNP153 22..33 33 - - - 98572 RMVar_ID_98572 Human_SNP_ID_103816654 m1A Human chr2 + 179264642 179264636 179264642 GGGGCGGAGCGGGCCCGGGCGGCGGCGGCAGCAGCGGCGACGGCTGCGGCTCCAGTCACTCGCGG GGGGCGGAGCGGGCCCGGGCGGCGGCG______GCGGCGACGGCTGCGGCTCCAGTCACTCGCGG GGCAGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr2:179264458..179264718;chr2:179264551..179264675 26863196,26863410 MeRIP-seq:(Medium) rs1285231329 Functional Loss DEL dbSNP153 28..33 33 - - - 98573 RMVar_ID_98573 Human_SNP_ID_103816658 m1A Human chr2 + 179264642 179264642 179264642 GGGGCGGAGCGGGCCCGGGCGGCGGCGGCAGCAGCGGCGACGGCTGCGGCTCCAGTCACTCGCGG GGGGCGGAGCGGGCCCGGGCGGCGGCGGCAGCGGCGGCGACGGCTGCGGCTCCAGTCACTCGCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr2:179264458..179264718;chr2:179264551..179264675 26863196,26863410 MeRIP-seq:(Medium) rs1363610551 Functional Loss SNV dbSNP153 33..33 33 - - - 98574 RMVar_ID_98574 Human_SNP_ID_103957536 m1A Human chr2 - 179861322 179861322 179861322 GGGCGCTTAAGCCCGGCGCGGGCAAGAGTTGGACAGTTCAGGGGCCGCGCCGGGCCGAGCTGTCG GGGCGCTTAAGCCCGGCGCGGGCAAGAGTTGGGCAGTTCAGGGGCCGCGCCGGGCCGAGCTGTCG T C ZNF385B Ensembl:ENSG00000144331 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:179861168..179861332 26863196 MeRIP-seq:(Medium) rs1026413950 Functional Loss SNV dbSNP153 33..33 33 - - - 98575 RMVar_ID_98575 Human_SNP_ID_715660898 m1A Human chrX - 45018037 45018037 45018037 TTCTTCTTCTACCCCTATTATTGCTCCTCCTCAGCTATAAACTGGCTTATCTCAGGAATTCTTAA TTCTTCTTCTACCCCTATTATTGCTCCTCCTCCGCTATAAACTGGCTTATCTCAGGAATTCTTAA T G RF00017-4675 RNACentral:URS00009156E9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:45017986..45018064 26863196 MeRIP-seq:(Medium) rs756633059 Functional Loss SNV dbSNP153 33..33 33 - - - 98576 RMVar_ID_98576 Human_SNP_ID_715805159 m1A Human chrX + 45850359 45850359 45850359 TTACCTCCTCCAAGTCCCACAGTCTACCTAGGACAAGTAAGCCCGGCTCCAGCACCTTAAGCCAA TTACCTCCTCCAAGTCCCACAGTCTACCTAGGGCAAGTAAGCCCGGCTCCAGCACCTTAAGCCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:45850346..45850476 26863196 MeRIP-seq:(Medium) rs782579866 Functional Loss SNV dbSNP153 33..33 33 - - - 98577 RMVar_ID_98577 Human_SNP_ID_715890497 m1A Human chrX - 46326423 46326423 46326423 GCACTTGGCCCTAAAGAGAAAACACTAGGAGGATGGGAACCAGGGACAGAGAAGCTACTTGCTCT GCACTTGGCCCTAAAGAGAAAACACTAGGAGGTTGGGAACCAGGGACAGAGAAGCTACTTGCTCT T A LINC01186 Ensembl:ENSG00000236751 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:46326320..46326475 26863196 MeRIP-seq:(Medium) rs1417168159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5638571 Human_Splice_Rec_2200570,Human_Splice_Rec_2200571,Human_Splice_Rec_2200576,Human_Splice_Rec_2200580,Human_Splice_Rec_2200581,Human_Splice_Rec_2200586 98578 RMVar_ID_98578 Human_SNP_ID_715890694 m1A Human chrX + 46327528 46327528 46327528 CCTCCCTTCCAACCTCCCAAATTAACACCACCATCTAAAACAAGAATTTGGTCACCTTTCGGAAG CCTCCCTTCCAACCTCCCAAATTAACACCACCGTCTAAAACAAGAATTTGGTCACCTTTCGGAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:46327526..46327622 26863196 MeRIP-seq:(Medium) rs886542025 Functional Loss SNV dbSNP153 33..33 33 - - - 98579 RMVar_ID_98579 Human_SNP_ID_715890703 m1A Human chrX - 46327596 46327596 46327596 GAGAGCGTGGGAAACCAGCAAGTTGAGAGAGGATCCAGAAGTAACCCCTTCTAAAACGGGAAAGA GAGAGCGTGGGAAACCAGCAAGTTGAGAGAGGTTCCAGAAGTAACCCCTTCTAAAACGGGAAAGA T A LINC01186 Ensembl:ENSG00000236751 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:46327496..46327651 26863196 MeRIP-seq:(Medium) rs1489720149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967728,Human_RBP_ID_5638573,Human_RBP_ID_18427842 Human_Splice_Rec_2200563,Human_Splice_Rec_2200569,Human_Splice_Rec_2200575,Human_Splice_Rec_2200579 98580 RMVar_ID_98580 Human_SNP_ID_715912843 m1A Human chrX - 46447348 46447344 46447348 ATCAAAACCATCACCACCTCCGCGTCCCTCTTACTTCACCGCCAAGAGCCTGAAACCTCAGAGGC ATCAAAACCATCACCACCTCCGCGTCCCTCTT____CACCGCCAAGAGCCTGAAACCTCAGAGGC GAAGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:46447323..46447423 26863196 MeRIP-seq:(Medium) rs1444929087 Functional Loss DEL dbSNP153 33..36 33 - - - 98581 RMVar_ID_98581 Human_SNP_ID_715912844 m1A Human chrX + 46447346 46447346 46447346 CGGCCTCTGAGGTTTCAGGCTCTTGGCGGTGAAGTAAGAGGGACGCGGAGGTGGTGATGGTTTTG CGGCCTCTGAGGTTTCAGGCTCTTGGCGGTGACGTAAGAGGGACGCGGAGGTGGTGATGGTTTTG A C KRBOX4 Ensembl:ENSG00000147121 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:46447317..46447407 26863196 MeRIP-seq:(Medium) rs1385236711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1342286 Human_Splice_Rec_2200588,Human_Splice_Rec_2200595,Human_Splice_Rec_2200607,Human_Splice_Rec_2200609,Human_Splice_Rec_2200617,Human_Splice_Rec_2200627 RMVar_hsa_circ_262197,RMVar_hsa_circ_128003 98582 RMVar_ID_98582 Human_SNP_ID_715933374 m1A Human chrX - 46575024 46575024 46575024 ATAGCGCAGCCTCAGGTAGCGGCGCCGCAGCCAGGCGGGCGCGCCGCGCGCGAAAAGCAGATCGC ATAGCGCAGCCTCAGGTAGCGGCGCCGCAGCCGGGCGGGCGCGCCGCGCGCGAAAAGCAGATCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:46574977..46575127 32194978 MeRIP-seq:(Medium) rs752194293 Functional Loss SNV dbSNP153 33..33 33 - - - 98583 RMVar_ID_98583 Human_SNP_ID_715976859 m1A Human chrX + 46837008 46837008 46837008 ACCGTTGGGCGGTTCCGCGGGGCGTTGTCCGGAGAGCTGCGAGGCCGGGGTTCCCAGGGTTCACG ACCGTTGGGCGGTTCCGCGGGGCGTTGTCCGGCGAGCTGCGAGGCCGGGGTTCCCAGGGTTCACG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:46836878..46837187 26863196 MeRIP-seq:(Medium) rs1346813814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076092,Human_RBP_ID_18920251 98584 RMVar_ID_98584 Human_SNP_ID_715976860 m1A Human chrX + 46837008 46837008 46837008 ACCGTTGGGCGGTTCCGCGGGGCGTTGTCCGGAGAGCTGCGAGGCCGGGGTTCCCAGGGTTCACG ACCGTTGGGCGGTTCCGCGGGGCGTTGTCCGGGGAGCTGCGAGGCCGGGGTTCCCAGGGTTCACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:46836878..46837187 26863196 MeRIP-seq:(Medium) rs1346813814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076092,Human_RBP_ID_18920251 98585 RMVar_ID_98585 Human_SNP_ID_715976879 m1A Human chrX + 46837079 46837079 46837079 TCTAGGAAGTGCCTGAGCTAGTGAGCTGGCCAACGAGCTCCGCGGGCTGGGACCATGGGCTGCTT TCTAGGAAGTGCCTGAGCTAGTGAGCTGGCCAGCGAGCTCCGCGGGCTGGGACCATGGGCTGCTT A G RP2 Ensembl:ENSG00000102218 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:46836971..46837187 26863196 MeRIP-seq:(Medium) rs782363029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735033,Human_RBP_ID_5064065 98586 RMVar_ID_98586 Human_SNP_ID_715988490 m1A Human chrX + 46912476 46912476 46912476 CTCCGCGCCGCCTCAGCCGCCGCCGCCGCCCAACCGCCTGCCCAGCGCTGAGGCCTGACGGGCCG CTCCGCGCCGCCTCAGCCGCCGCCGCCGCCCAGCCGCCTGCCCAGCGCTGAGGCCTGACGGGCCG A G JADE3 Ensembl:ENSG00000102221 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:46912426..46912605 26863196 MeRIP-seq:(Medium) rs1290908222 Functional Loss SNV dbSNP153 33..33 33 - - - 98587 RMVar_ID_98587 Human_SNP_ID_715988545 m1A Human chrX + 46912664 46912664 46912664 GGCGGTTACCACTCCGACCGGACTCACCCGGCACATTGCCGGGCCGCGGCGTGGAGCCGGGCAGG GGCGGTTACCACTCCGACCGGACTCACCCGGCGCATTGCCGGGCCGCGGCGTGGAGCCGGGCAGG A G JADE3 Ensembl:ENSG00000102221 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:46912579..46912717 26863410 MeRIP-seq:(Medium) rs1330564900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257928,Human_RBP_ID_5075794,Human_RBP_ID_9443288,Human_RBP_ID_18427941,Human_RBP_ID_18468223 Human_Splice_Rec_2200839 98588 RMVar_ID_98588 Human_SNP_ID_715996029 m1A Human chrX - 46959670 46959670 46959670 CTCATCATCACCCTATCCTACTTCACATGGCTATCTCCTAGTCATGTCAGATTTCAATCCAAACA CTCATCATCACCCTATCCTACTTCACATGGCTGTCTCCTAGTCATGTCAGATTTCAATCCAAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:46959667..46959770 26863196 MeRIP-seq:(Medium) rs1230780133 Functional Loss SNV dbSNP153 33..33 33 - - - 98589 RMVar_ID_98589 Human_SNP_ID_716028126 m1A Human chrX + 47144552 47144552 47144552 GTGTGGTCGGTTCTGGGGGCCGCTTTCCCGCCACAGCGGACGGGGCGACCACAGTCCTGGAGAAG GTGTGGTCGGTTCTGGGGGCCGCTTTCCCGCCCCAGCGGACGGGGCGACCACAGTCCTGGAGAAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47144501..47144650 32194978 MeRIP-seq:(Medium) rs111877073 Functional Loss SNV dbSNP153 33..33 33 - - - 98590 RMVar_ID_98590 Human_SNP_ID_716028137 m1A Human chrX - 47144586 47144586 47144586 GGCTCCCGGCCGCCCGCGTCCGCTGGGAATCTAGCTTCTCCAGGACTGTGGTCGCCCCGTCCGCT GGCTCCCGGCCGCCCGCGTCCGCTGGGAATCTGGCTTCTCCAGGACTGTGGTCGCCCCGTCCGCT T C NDUFB11 Ensembl:ENSG00000147123 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:47144535..47144725 26863196 MeRIP-seq:(Medium) rs1281988503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735095,Human_RBP_ID_5064192,Human_RBP_ID_9339924,Human_RBP_ID_17667408,Human_RBP_ID_18197278,Human_RBP_ID_22467532,Human_RBP_ID_23217156 Human_miRNA_ID_2056937 RMVar_hsa_circ_83442,RMVar_hsa_circ_262236 98591 RMVar_ID_98591 Human_SNP_ID_716028223 m1A Human chrX - 47144954 47144954 47144954 GAACTCGGGGCGATTGGCTGGGAACTGTATCCACCCAAATGTCACCGATTTCTTCCTATGCAGGA GAACTCGGGGCGATTGGCTGGGAACTGTATCCTCCCAAATGTCACCGATTTCTTCCTATGCAGGA T A NDUFB11 Ensembl:ENSG00000147123 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:47144903..47144990 26863196 MeRIP-seq:(Medium) rs782472450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27571161 RMVar_hsa_circ_83442,RMVar_hsa_circ_262236 98592 RMVar_ID_98592 Human_SNP_ID_716028317 m1A Human chrX - 47145462 47145458 47145462 GACGCTCACCTTCTCGGCCCGGGCTGTCAAGGAAGGGCTCCCAGACATCACCTCTGCCCGCCGCC GACGCTCACCTTCTCGGCCCGGGCTGTCAAGG____GCTCCCAGACATCACCTCTGCCCGCCGCC CCCTT C NDUFB11 Ensembl:ENSG00000147123 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47145308..47145504 32194978 MeRIP-seq:(Medium) rs1556761618 Functional Loss DEL dbSNP153 33..36 33 - - - 98593 RMVar_ID_98593 Human_SNP_ID_716028318 m1A Human chrX - 47145462 47145462 47145462 GACGCTCACCTTCTCGGCCCGGGCTGTCAAGGAAGGGCTCCCAGACATCACCTCTGCCCGCCGCC GACGCTCACCTTCTCGGCCCGGGCTGTCAAGGGAGGGCTCCCAGACATCACCTCTGCCCGCCGCC T C NDUFB11 Ensembl:ENSG00000147123 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47145308..47145504 32194978 MeRIP-seq:(Medium) rs5952419 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_603,Clinvar_Rec_604 98594 RMVar_ID_98594 Human_SNP_ID_716033566 m1A Human chrX - 47174699 47174699 47174699 GGCAGACCTGCCCAGCCAGCCTGGGGTGACAGAGACGGAGAGAAGCAGCTGGGAGGGAAAGAATA GGCAGACCTGCCCAGCCAGCCTGGGGTGACAGGGACGGAGAGAAGCAGCTGGGAGGGAAAGAATA T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:47174692..47174812 26863196 MeRIP-seq:(Medium) rs1053463798 Functional Loss SNV dbSNP153 33..33 33 - - - 98595 RMVar_ID_98595 Human_SNP_ID_716034299 m1A Human chrX + 47178809 47178809 47178809 ATTGAATACCTGAGGCGGGGAACAGTCCTGGGAGTTGGTGGCCTTAAGAAGGCAGAGGAAGGAGA ATTGAATACCTGAGGCGGGGAACAGTCCTGGGCGTTGGTGGCCTTAAGAAGGCAGAGGAAGGAGA A C RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:47178803..47178929 26863196 MeRIP-seq:(Medium) rs941747623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_810,RMVar_hsa_circ_102575,RMVar_hsa_circ_262239,RMVar_hsa_circ_104340,RMVar_hsa_circ_262240 98596 RMVar_ID_98596 Human_SNP_ID_716035810 m1A Human chrX + 47186325 47186325 47186325 GTGACAACATTGGCAGTCGGATGCTGCAGGCCATGGGCTGGAAAGAGGGCAGCGGCCTGGGCCGC GTGACAACATTGGCAGTCGGATGCTGCAGGCCGTGGGCTGGAAAGAGGGCAGCGGCCTGGGCCGC A G RBM10 Ensembl:ENSG00000182872 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:47186126..47186409 26863196 MeRIP-seq:(Medium) rs1556782610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799833,Human_RBP_ID_5064305,Human_RBP_ID_27834390 Human_Splice_Rec_2200975,Human_Splice_Rec_2200976,Human_Splice_Rec_2201017,Human_Splice_Rec_2201018,Human_Splice_Rec_2201061,Human_Splice_Rec_2201062,Human_Splice_Rec_2201107,Human_Splice_Rec_2201108 Human_miRNA_ID_2975376,Human_miRNA_ID_3008571 RMVar_hsa_circ_102575,RMVar_hsa_circ_262239,RMVar_hsa_circ_81627,RMVar_hsa_circ_262242,RMVar_hsa_circ_123160,RMVar_hsa_circ_126634,RMVar_hsa_circ_262243,RMVar_hsa_circ_262244,RMVar_hsa_circ_100246,RMVar_hsa_circ_116080,RMVar_hsa_circ_262247,RMVar_hsa_circ_262248,RMVar_hsa_circ_79666,RMVar_hsa_circ_375545,RMVar_hsa_circ_262249,RMVar_hsa_circ_262250 98597 RMVar_ID_98597 Human_SNP_ID_716036561 m1A Human chrX - 47190952 47190952 47190952 TCCAGAGGCTTGGGGGCACGGTGCTCCAGCTCACCCCCTGTGCCGGGCGGAAGCCTCGCCTTCCT TCCAGAGGCTTGGGGGCACGGTGCTCCAGCTCTCCCCCTGTGCCGGGCGGAAGCCTCGCCTTCCT T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:47190876..47190975 26863410 MeRIP-seq:(Medium) rs1031256887 Functional Loss SNV dbSNP153 33..33 33 - - - 98598 RMVar_ID_98598 Human_SNP_ID_716036592 m1A Human chrX - 47191143 47191142 47191144 AAACCCTGCCTCCGAGGGGTGCTCCCCGAAACAGACTCCCAAATCCCACCCCGAAGTCCCCAAAC AAACCCTGCCTCCGAGGGGTGCTCCCCGAAA__GACTCCCAAATCCCACCCCGAAGTCCCCAAAC CTG C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:47191141..47191242 26863196 MeRIP-seq:(Medium) rs1411839623 Functional Loss DEL dbSNP153 32..33 33 - - - 98599 RMVar_ID_98599 Human_SNP_ID_716038765 m1A Human chrX + 47202449 47202449 47202449 TTCTCGCCCTGCCCAGCTGCACATTGGCTTCCAGGCCCTGCACCAGTTCTGTGCTCAGCATGGCC TTCTCGCCCTGCCCAGCTGCACATTGGCTTCCCGGCCCTGCACCAGTTCTGTGCTCAGCATGGCC A C UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:47202426..47202450 26863196 MeRIP-seq:(Medium) rs782442496 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_93913,Human_RBP_ID_735128,Human_RBP_ID_968598,Human_RBP_ID_3976429,Human_RBP_ID_8719373,Human_RBP_ID_8938630,Human_RBP_ID_9317311,Human_RBP_ID_18920391,Human_RBP_ID_22426756,Human_RBP_ID_22467540,Human_RBP_ID_22778103 Human_Splice_Rec_2201148,Human_Splice_Rec_2201234,Human_Splice_Rec_2201235 Human_miRNA_ID_2575483,Human_miRNA_ID_2921484,Human_miRNA_ID_3005098 RMVar_hsa_circ_20668,RMVar_hsa_circ_90636,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_359980,RMVar_hsa_circ_317621,RMVar_hsa_circ_64133,RMVar_hsa_circ_28136,RMVar_hsa_circ_38306,RMVar_hsa_circ_108583,RMVar_hsa_circ_118943,RMVar_hsa_circ_122703,RMVar_hsa_circ_262254,RMVar_hsa_circ_262255,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_262256,RMVar_hsa_circ_117893,RMVar_hsa_circ_127422,RMVar_hsa_circ_262259,RMVar_hsa_circ_262260,RMVar_hsa_circ_262258,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262263,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_10085,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,RMVar_hsa_circ_262268,RMVar_hsa_circ_266057,RMVar_hsa_circ_106398,RMVar_hsa_circ_116055,RMVar_hsa_circ_85657,RMVar_hsa_circ_262270,RMVar_hsa_circ_262271,RMVar_hsa_circ_262272 98600 RMVar_ID_98600 Human_SNP_ID_716038986 m1A Human chrX + 47203184 47203184 47203184 GGGCAAGTGGCTGTGTTTGGCTCAGACCTGCAAGAGAAGCTGGGCAAGCAGAAGTATTTCCTGGT GGGCAAGTGGCTGTGTTTGGCTCAGACCTGCAGGAGAAGCTGGGCAAGCAGAAGTATTTCCTGGT A G UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:47203125..47203232 26863196 MeRIP-seq:(Medium) rs781891689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93917,Human_RBP_ID_1715338,Human_RBP_ID_8239876,Human_RBP_ID_16896933,Human_RBP_ID_24343095,Human_RBP_ID_27834392 Human_Splice_Rec_2201152,Human_Splice_Rec_2201153,Human_Splice_Rec_2201240,Human_Splice_Rec_2201241,Human_Splice_Rec_2201289,Human_Splice_Rec_2201290 Human_miRNA_ID_3119377 RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_359980,RMVar_hsa_circ_317621,RMVar_hsa_circ_64133,RMVar_hsa_circ_28136,RMVar_hsa_circ_38306,RMVar_hsa_circ_108583,RMVar_hsa_circ_118943,RMVar_hsa_circ_122703,RMVar_hsa_circ_262255,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_262256,RMVar_hsa_circ_127422,RMVar_hsa_circ_262259,RMVar_hsa_circ_262260,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262263,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,RMVar_hsa_circ_262268,RMVar_hsa_circ_266057,RMVar_hsa_circ_106398,RMVar_hsa_circ_85657,RMVar_hsa_circ_122061,RMVar_hsa_circ_262271,RMVar_hsa_circ_262272,RMVar_hsa_circ_105010,RMVar_hsa_circ_262275,RMVar_hsa_circ_262276 98601 RMVar_ID_98601 Human_SNP_ID_716040734 m1A Human chrX + 47211082 47211082 47211082 CTATGTGATGGCTGCTGCCAACCTGTTTGCCCAGACCTACGGGCTGACAGGCTCTCAGGACCGAG CTATGTGATGGCTGCTGCCAACCTGTTTGCCCGGACCTACGGGCTGACAGGCTCTCAGGACCGAG A G UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1556793231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735141,Human_RBP_ID_799576,Human_RBP_ID_5230823,Human_RBP_ID_8163447,Human_RBP_ID_8719398,Human_RBP_ID_8938643,Human_RBP_ID_9316758,Human_RBP_ID_17326341,Human_RBP_ID_17442689,Human_RBP_ID_18454395,Human_RBP_ID_18920428,Human_RBP_ID_19026576,Human_RBP_ID_22468714,Human_RBP_ID_26772771 Human_Splice_Rec_2201166,Human_Splice_Rec_2201254,Human_Splice_Rec_2201301 Human_miRNA_ID_2225926 RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_118943,RMVar_hsa_circ_262260,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_262268,RMVar_hsa_circ_122061,RMVar_hsa_circ_105010,RMVar_hsa_circ_262275,RMVar_hsa_circ_94603,RMVar_hsa_circ_262276,RMVar_hsa_circ_262277,RMVar_hsa_circ_262280,RMVar_hsa_circ_125187,RMVar_hsa_circ_262278,RMVar_hsa_circ_302992,RMVar_hsa_circ_262281,RMVar_hsa_circ_262282,RMVar_hsa_circ_127935,RMVar_hsa_circ_94543,RMVar_hsa_circ_262284,RMVar_hsa_circ_262286,RMVar_hsa_circ_84920,RMVar_hsa_circ_262285 98602 RMVar_ID_98602 Human_SNP_ID_716040745 m1A Human chrX + 47211126 47211126 47211126 TGACAGGCTCTCAGGACCGAGCTGCTGTGGCCACATTCCTGCAGTCTGTGCAGGTCCCCGAATTC TGACAGGCTCTCAGGACCGAGCTGCTGTGGCCCCATTCCTGCAGTCTGTGCAGGTCCCCGAATTC A C UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:47211101..47211125 26863196 MeRIP-seq:(Medium) rs377527446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735142,Human_RBP_ID_1230730,Human_RBP_ID_5082491,Human_RBP_ID_8935761,Human_RBP_ID_9265260,Human_RBP_ID_9316759,Human_RBP_ID_17326342,Human_RBP_ID_17442690,Human_RBP_ID_22467907,Human_RBP_ID_23108627,Human_RBP_ID_26280746,Human_RBP_ID_27148386 Human_Splice_Rec_2201166,Human_Splice_Rec_2201167,Human_Splice_Rec_2201254,Human_Splice_Rec_2201255,Human_Splice_Rec_2201301,Human_Splice_Rec_2201302 Human_miRNA_ID_1934252,Human_miRNA_ID_2198059,Human_miRNA_ID_2676440,Human_miRNA_ID_2927194,Human_miRNA_ID_2937069 RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_118943,RMVar_hsa_circ_262260,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_262268,RMVar_hsa_circ_122061,RMVar_hsa_circ_105010,RMVar_hsa_circ_262275,RMVar_hsa_circ_94603,RMVar_hsa_circ_262276,RMVar_hsa_circ_262277,RMVar_hsa_circ_262280,RMVar_hsa_circ_125187,RMVar_hsa_circ_262278,RMVar_hsa_circ_302992,RMVar_hsa_circ_262281,RMVar_hsa_circ_262282,RMVar_hsa_circ_127935,RMVar_hsa_circ_94543,RMVar_hsa_circ_262284,RMVar_hsa_circ_262286,RMVar_hsa_circ_84920,RMVar_hsa_circ_262285 98603 RMVar_ID_98603 Human_SNP_ID_716040746 m1A Human chrX + 47211126 47211126 47211126 TGACAGGCTCTCAGGACCGAGCTGCTGTGGCCACATTCCTGCAGTCTGTGCAGGTCCCCGAATTC TGACAGGCTCTCAGGACCGAGCTGCTGTGGCCGCATTCCTGCAGTCTGTGCAGGTCCCCGAATTC A G UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:47211101..47211125 26863196 MeRIP-seq:(Medium) rs377527446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735142,Human_RBP_ID_1230730,Human_RBP_ID_5082491,Human_RBP_ID_8935761,Human_RBP_ID_9265260,Human_RBP_ID_9316759,Human_RBP_ID_17326342,Human_RBP_ID_17442690,Human_RBP_ID_22467907,Human_RBP_ID_23108627,Human_RBP_ID_26280746,Human_RBP_ID_27148386 Human_Splice_Rec_2201166,Human_Splice_Rec_2201167,Human_Splice_Rec_2201254,Human_Splice_Rec_2201255,Human_Splice_Rec_2201301,Human_Splice_Rec_2201302 Human_miRNA_ID_1934252,Human_miRNA_ID_2198059,Human_miRNA_ID_2676440,Human_miRNA_ID_2927194,Human_miRNA_ID_2937069 RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_118943,RMVar_hsa_circ_262260,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_262268,RMVar_hsa_circ_122061,RMVar_hsa_circ_105010,RMVar_hsa_circ_262275,RMVar_hsa_circ_94603,RMVar_hsa_circ_262276,RMVar_hsa_circ_262277,RMVar_hsa_circ_262280,RMVar_hsa_circ_125187,RMVar_hsa_circ_262278,RMVar_hsa_circ_302992,RMVar_hsa_circ_262281,RMVar_hsa_circ_262282,RMVar_hsa_circ_127935,RMVar_hsa_circ_94543,RMVar_hsa_circ_262284,RMVar_hsa_circ_262286,RMVar_hsa_circ_84920,RMVar_hsa_circ_262285 98604 RMVar_ID_98604 Human_SNP_ID_716041559 m1A Human chrX - 47214958 47214958 47214958 CTGGGCTGGAAGGGGTGTGGAGAGGGGTGGACAAGGGGCCAGCCTAGAGGAGCAGACGGGGTCAG CTGGGCTGGAAGGGGTGTGGAGAGGGGTGGACGAGGGGCCAGCCTAGAGGAGCAGACGGGGTCAG T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:47214776..47215075 26863410 MeRIP-seq:(Medium) rs1034629286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262289 98605 RMVar_ID_98605 Human_SNP_ID_716041562 m1A Human chrX - 47214968 47214966 47214968 AATGGGAACCCTGGGCTGGAAGGGGTGTGGAGAGGGGTGGACAAGGGGCCAGCCTAGAGGAGCAG AATGGGAACCCTGGGCTGGAAGGGGTGTGGAG__GGGTGGACAAGGGGCCAGCCTAGAGGAGCAG CCT C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:47214883..47215035 26863196 MeRIP-seq:(Medium) rs781965236 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_262289 98606 RMVar_ID_98606 Human_SNP_ID_716042349 m1A Human chrX + 47218840 47218840 47218840 CGCCGTGAGCACTCGGATTCAAGCCGGCGCCAACGAGTCCGGGGGCATCGCCCGCAGCGGCCAAG CGCCGTGAGCACTCGGATTCAAGCCGGCGCCAGCGAGTCCGGGGGCATCGCCCGCAGCGGCCAAG A G CDK16 Ensembl:ENSG00000102225 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:47218726..47219142 26863196 MeRIP-seq:(Medium) rs1387065533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257245,Human_RBP_ID_848393,Human_RBP_ID_5064572,Human_RBP_ID_5432172 RMVar_hsa_circ_262292,RMVar_hsa_circ_115498,RMVar_hsa_circ_86894,RMVar_hsa_circ_262291 98607 RMVar_ID_98607 Human_SNP_ID_716042364 m1A Human chrX - 47218901 47218895 47218901 GGAGGCGGCGGCGGCGGCGGTGGCTGAGGCGGAGGCGGCGTCCCGCTCAGCCGGCCATGAGCTTG GGAGGCGGCGGCGGCGGCGGTGGCTGAGGCGG______CGTCCCGCTCAGCCGGCCATGAGCTTG GCCGCCT G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:47218726..47219112 26863410 MeRIP-seq:(Medium) rs1201082250 Functional Loss DEL dbSNP153 33..38 33 - - - 98608 RMVar_ID_98608 Human_SNP_ID_716042365 m1A Human chrX - 47218901 47218901 47218901 GGAGGCGGCGGCGGCGGCGGTGGCTGAGGCGGAGGCGGCGTCCCGCTCAGCCGGCCATGAGCTTG GGAGGCGGCGGCGGCGGCGGTGGCTGAGGCGGCGGCGGCGTCCCGCTCAGCCGGCCATGAGCTTG T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:47218726..47219112 26863410 MeRIP-seq:(Medium) rs1556796301 Functional Loss SNV dbSNP153 33..33 33 - - - 98609 RMVar_ID_98609 Human_SNP_ID_716043236 m1A Human chrX - 47223553 47223553 47223553 GCCGTTTGATCTTCTTCATCCGATCCATGGCGATCTGAGCAAGGGACAAGGATGGAAATGGGTCT GCCGTTTGATCTTCTTCATCCGATCCATGGCGCTCTGAGCAAGGGACAAGGATGGAAATGGGTCT T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:47223551..47223600 26863196 MeRIP-seq:(Medium) rs1248550846 Functional Loss SNV dbSNP153 33..33 33 - - - 98610 RMVar_ID_98610 Human_SNP_ID_716043262 m1A Human chrX + 47223646 47223646 47223646 AGGCATAGACAAGACCAATGGTGCCCCTGAGCAGATAGGCCTGGATGAGAGTGGTGGTGGTGGCG AGGCATAGACAAGACCAATGGTGCCCCTGAGCTGATAGGCCTGGATGAGAGTGGTGGTGGTGGCG A T CDK16 Ensembl:ENSG00000102225 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:47223601..47223675 26863196 MeRIP-seq:(Medium) rs745553260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735174,Human_RBP_ID_799331,Human_RBP_ID_5082523,Human_RBP_ID_5637664,Human_RBP_ID_8005690,Human_RBP_ID_8719432,Human_RBP_ID_16897370,Human_RBP_ID_17718364,Human_RBP_ID_18197285,Human_RBP_ID_19026579,Human_RBP_ID_22468720,Human_RBP_ID_22631857,Human_RBP_ID_27552000 Human_Splice_Rec_2201323,Human_Splice_Rec_2201353,Human_Splice_Rec_2201355,Human_Splice_Rec_2201359,Human_Splice_Rec_2201390,Human_Splice_Rec_2201398,Human_Splice_Rec_2201404,Human_Splice_Rec_2201435,Human_Splice_Rec_2201457,Human_Splice_Rec_2201471,Human_Splice_Rec_2201501,Human_Splice_Rec_2201531 RMVar_hsa_circ_262292,RMVar_hsa_circ_115498,RMVar_hsa_circ_86894,RMVar_hsa_circ_54231,RMVar_hsa_circ_262291,RMVar_hsa_circ_311251 98611 RMVar_ID_98611 Human_SNP_ID_716043269 m1A Human chrX - 47223674 47223674 47223674 CGTGTGGGGGCCTCTCCAGGGTCACTGCCGCCACCACCACCACTCTCATCCAGGCCTATCTGCTC CGTGTGGGGGCCTCTCCAGGGTCACTGCCGCCGCCACCACCACTCTCATCCAGGCCTATCTGCTC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:47223651..47223675 26863196 MeRIP-seq:(Medium) rs777199690 Functional Loss SNV dbSNP153 33..33 33 - - - 98612 RMVar_ID_98612 Human_SNP_ID_716043441 m1A Human chrX + 47224489 47224489 47224489 AGGTGCAGTCTCCAGTGAGAGTGCGTATGCGCAACCATCCCCCACGCAAGATCTCCACTGAGGTG AGGTGCAGTCTCCAGTGAGAGTGCGTATGCGCGACCATCCCCCACGCAAGATCTCCACTGAGGTG A G CDK16 Ensembl:ENSG00000102225 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:47224374..47224535 26863196 MeRIP-seq:(Medium) rs779886300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19027244,Human_RBP_ID_26834673 Human_Splice_Rec_2201326,Human_Splice_Rec_2201362,Human_Splice_Rec_2201393,Human_Splice_Rec_2201401,Human_Splice_Rec_2201408,Human_Splice_Rec_2201438,Human_Splice_Rec_2201460,Human_Splice_Rec_2201474,Human_Splice_Rec_2201482,Human_Splice_Rec_2201504,Human_Splice_Rec_2201534 Human_miRNA_ID_1957886,Human_miRNA_ID_2653798,Human_miRNA_ID_2754995 RMVar_hsa_circ_262292,RMVar_hsa_circ_115498,RMVar_hsa_circ_86894,RMVar_hsa_circ_54231,RMVar_hsa_circ_262291,RMVar_hsa_circ_311251 98613 RMVar_ID_98613 Human_SNP_ID_716043550 m1A Human chrX + 47225031 47225031 47225031 CACCGTCTACAAAGGCAAAAGCAAGCTCACAGACAACCTTGTGGCACTCAAGGAGATCAGACTGG CACCGTCTACAAAGGCAAAAGCAAGCTCACAGGCAACCTTGTGGCACTCAAGGAGATCAGACTGG A G CDK16 Ensembl:ENSG00000102225 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:47224363..47225099 26863196 MeRIP-seq:(Medium) rs1264123488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1715400,Human_RBP_ID_2075051,Human_RBP_ID_8005703,Human_RBP_ID_8935782,Human_RBP_ID_16897379,Human_RBP_ID_17326352,Human_RBP_ID_17441537,Human_RBP_ID_17554592,Human_RBP_ID_18920493,Human_RBP_ID_27163446 Human_Splice_Rec_2201331,Human_Splice_Rec_2201332,Human_Splice_Rec_2201367,Human_Splice_Rec_2201368,Human_Splice_Rec_2201413,Human_Splice_Rec_2201414,Human_Splice_Rec_2201443,Human_Splice_Rec_2201444,Human_Splice_Rec_2201465,Human_Splice_Rec_2201466,Human_Splice_Rec_2201479,Human_Splice_Rec_2201487,Human_Splice_Rec_2201488,Human_Splice_Rec_2201509,Human_Splice_Rec_2201510,Human_Splice_Rec_2201539,Human_Splice_Rec_2201540,Human_Splice_Rec_2201567 Human_miRNA_ID_2673668,Human_miRNA_ID_2673669,Human_miRNA_ID_2942913,Human_miRNA_ID_2942914 RMVar_hsa_circ_14926,RMVar_hsa_circ_262292,RMVar_hsa_circ_115498,RMVar_hsa_circ_86894,RMVar_hsa_circ_54231,RMVar_hsa_circ_262291,RMVar_hsa_circ_311251,RMVar_hsa_circ_114371,RMVar_hsa_circ_82865,RMVar_hsa_circ_262295,RMVar_hsa_circ_262296,RMVar_hsa_circ_262294 98614 RMVar_ID_98614 Human_SNP_ID_716044350 m1A Human chrX + 47228803 47228803 47228803 CACAGACCGAGGCCCCAGCAGGCAGCGGCTGGAGGGATGCCACACCCCTCACAGGGCAGCCCCCA CACAGACCGAGGCCCCAGCAGGCAGCGGCTGGGGGGATGCCACACCCCTCACAGGGCAGCCCCCA A G CDK16 Ensembl:ENSG00000102225 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:47228681..47228925 26863196 MeRIP-seq:(Medium) rs199882440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735199,Human_RBP_ID_799344,Human_RBP_ID_848395,Human_RBP_ID_3976442,Human_RBP_ID_5124715,Human_RBP_ID_8005727,Human_RBP_ID_17442699,Human_RBP_ID_17556129,Human_RBP_ID_19026586 Human_Splice_Rec_2201350,Human_Splice_Rec_2201386,Human_Splice_Rec_2201433,Human_Splice_Rec_2201529,Human_Splice_Rec_2201559,Human_Splice_Rec_2201583,Human_Splice_Rec_2201607,Human_Splice_Rec_2201615 Human_miRNA_ID_445979,Human_miRNA_ID_1562483,Human_miRNA_ID_2154076,Human_miRNA_ID_2422232,Human_miRNA_ID_2801950,Human_miRNA_ID_2975377,Human_miRNA_ID_3008572,Human_miRNA_ID_3010083 RMVar_hsa_circ_114371,RMVar_hsa_circ_262296 98615 RMVar_ID_98615 Human_SNP_ID_716045185 m1A Human chrX - 47233076 47233076 47233076 GTCACCGCCGCTGCCGCCGCCACAGCCGCCGCAGCAGCAGCTGGATTTGCTGCGACCGTCGCCAT GTCACCGCCGCTGCCGCCGCCACAGCCGCCGCCGCAGCAGCTGGATTTGCTGCGACCGTCGCCAT T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:47233026..47233200;chrX:47233026..47233272;chrX:47233026..47233267 26863196 MeRIP-seq:(Medium) rs918867462 Functional Loss SNV dbSNP153 33..33 33 - - - 98616 RMVar_ID_98616 Human_SNP_ID_716046367 m1A Human chrX - 47239052 47239052 47239052 TTCTCCACAAGGAACCTGGGGCCCAGACAGGTAACAAGGGTGTTACATGGGTAGCTGAGGGTTAG TTCTCCACAAGGAACCTGGGGCCCAGACAGGTTACAAGGGTGTTACATGGGTAGCTGAGGGTTAG T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47239051..47239150 32194978 MeRIP-seq:(Medium) rs1325762797 Functional Loss SNV dbSNP153 33..33 33 - - - 98617 RMVar_ID_98617 Human_SNP_ID_716088662 m1A Human chrX - 47462350 47462350 47462350 AAGGAAAAGTCAGAGGGAACAACGACCAGCAAAGGGAGCAGGGACAGATCTGGGCAGGCAGCAAA AAGGAAAAGTCAGAGGGAACAACGACCAGCAATGGGAGCAGGGACAGATCTGGGCAGGCAGCAAA T A ZNF41 Ensembl:ENSG00000147124 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:47462320..47462435 26863196 MeRIP-seq:(Medium) rs955199925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262319,RMVar_hsa_circ_34863 98618 RMVar_ID_98618 Human_SNP_ID_716089025 m1A Human chrX - 47464152 47464152 47464152 AGGGAAGAGCCGAGGGTTAAAGAACAGTGAGAAGGATCATGAAATAGGAGGAGGTATCAGGAAAT AGGGAAGAGCCGAGGGTTAAAGAACAGTGAGATGGATCATGAAATAGGAGGAGGTATCAGGAAAT T A ZNF41 Ensembl:ENSG00000147124 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:47463452..47464447;chrX:47463468..47464419 26863196 MeRIP-seq:(Medium) rs747972815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262319,RMVar_hsa_circ_34863 98619 RMVar_ID_98619 Human_SNP_ID_716105468 m1A Human chrX + 47561250 47561250 47561250 GATGGAGACGGCGGCGGCTGTAGCGGCGTGACAGGTGAGGGCGGGCCCGGGAGGGCTCGGTTTCT GATGGAGACGGCGGCGGCTGTAGCGGCGTGACCGGTGAGGGCGGGCCCGGGAGGGCTCGGTTTCT A C ARAF Ensembl:ENSG00000078061 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:47561201..47561443;chrX:47561201..47561488;chrX:47561201..47561486 26863196 MeRIP-seq:(Medium) rs1375600064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19148322 Human_Splice_Rec_2201836,Human_Splice_Rec_2201864,Human_Splice_Rec_2201893 98620 RMVar_ID_98620 Human_SNP_ID_716107066 m1A Human chrX + 47568789 47568789 47568789 CATGACCCGGCCGGGATTTGCCATCATCACACAGTGGTGTGAGGGCTCCAGCCTCTACCATCACC CATGACCCGGCCGGGATTTGCCATCATCACACGGTGGTGTGAGGGCTCCAGCCTCTACCATCACC A G ARAF Ensembl:ENSG00000078061 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:47568739..47568889 32194978 MeRIP-seq:(Medium) rs778119620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735314,Human_RBP_ID_26834690,Human_RBP_ID_27148560 Human_Splice_Rec_2201854,Human_Splice_Rec_2201883 Human_miRNA_ID_1003330,Human_miRNA_ID_1167489,Human_miRNA_ID_1398246,Human_miRNA_ID_2451275,Human_miRNA_ID_2716868 RMVar_hsa_circ_103264,RMVar_hsa_circ_126962,RMVar_hsa_circ_262322,RMVar_hsa_circ_39614,RMVar_hsa_circ_262323 98621 RMVar_ID_98621 Human_SNP_ID_716107699 m1A Human chrX + 47571506 47571506 47571506 CAGGGAGCCAATCTCAGCCCTCCACGCCAAGGAGCCTTGCCCACCAGCCAATCAATGTTCGTCTC CAGGGAGCCAATCTCAGCCCTCCACGCCAAGGGGCCTTGCCCACCAGCCAATCAATGTTCGTCTC A G ARAF Ensembl:ENSG00000078061 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:47571351..47571575 26863196 MeRIP-seq:(Medium) rs1413482936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735318,Human_RBP_ID_5124719 Human_miRNA_ID_2053127,Human_miRNA_ID_2219064,Human_miRNA_ID_2874491,Human_miRNA_ID_2982451 RMVar_hsa_circ_103264,RMVar_hsa_circ_126962,RMVar_hsa_circ_262322,RMVar_hsa_circ_262323 98622 RMVar_ID_98622 Human_SNP_ID_716110127 m1A Human chrX + 47583499 47583499 47583499 ATAGCCCCCAGCAGGGCCTGCACCTGTGTCCCACCCCACCCACAGACGGCCTTCTGCAATTCCGA ATAGCCCCCAGCAGGGCCTGCACCTGTGTCCCGCCCCACCCACAGACGGCCTTCTGCAATTCCGA A G TIMP1 Ensembl:ENSG00000102265 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:47583401..47583550 26863196 MeRIP-seq:(Medium) rs1287670583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93574,Human_RBP_ID_1405736,Human_RBP_ID_9339936,Human_RBP_ID_22467563,Human_RBP_ID_26834692 Human_Splice_Rec_2202002,Human_Splice_Rec_2202003,Human_Splice_Rec_2202007,Human_Splice_Rec_2202024,Human_Splice_Rec_2202025 RMVar_hsa_circ_104682,RMVar_hsa_circ_83911,RMVar_hsa_circ_108318,RMVar_hsa_circ_262324,RMVar_hsa_circ_262325,RMVar_hsa_circ_121263,RMVar_hsa_circ_262326,RMVar_hsa_circ_262327 98623 RMVar_ID_98623 Human_SNP_ID_716110138 m1A Human chrX - 47583538 47583538 47583538 CAGAGTGTGTGGGCTGAGTGGGGTGAGGACTCACCGAGGTCGGAATTGCAGAAGGCCGTCTGTGG CAGAGTGTGTGGGCTGAGTGGGGTGAGGACTCTCCGAGGTCGGAATTGCAGAAGGCCGTCTGTGG T A SYN1,Z84466.1 Ensembl:ENSG00000008056,Ensembl:ENSG00000283743 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:47583501..47583550 26863196 MeRIP-seq:(Medium) rs111842085 Functional Loss SNV dbSNP153 33..33 33 - - - 98624 RMVar_ID_98624 Human_SNP_ID_716110139 m1A Human chrX - 47583538 47583538 47583538 CAGAGTGTGTGGGCTGAGTGGGGTGAGGACTCACCGAGGTCGGAATTGCAGAAGGCCGTCTGTGG CAGAGTGTGTGGGCTGAGTGGGGTGAGGACTCGCCGAGGTCGGAATTGCAGAAGGCCGTCTGTGG T C SYN1,Z84466.1 Ensembl:ENSG00000008056,Ensembl:ENSG00000283743 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:47583501..47583550 26863196 MeRIP-seq:(Medium) rs111842085 Functional Loss SNV dbSNP153 33..33 33 - - - 98625 RMVar_ID_98625 Human_SNP_ID_716110378 m1A Human chrX + 47584967 47584967 47584967 GTCATCAGGGCCAAGTTCGTGGGGACACCAGAAGTCAACCAGACCACCTTATACCAGCGTTATGA GTCATCAGGGCCAAGTTCGTGGGGACACCAGACGTCAACCAGACCACCTTATACCAGCGTTATGA A C TIMP1 Ensembl:ENSG00000102265 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:47584926..47585000;chrX:47584926..47585025 26863196 MeRIP-seq:(Medium) rs141614092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93575,Human_RBP_ID_735331,Human_RBP_ID_798990,Human_RBP_ID_968587,Human_RBP_ID_2075159,Human_RBP_ID_18197288,Human_RBP_ID_22467564,Human_RBP_ID_22693225,Human_RBP_ID_26835415 Human_Splice_Rec_2202004,Human_Splice_Rec_2202008,Human_Splice_Rec_2202009,Human_Splice_Rec_2202016,Human_Splice_Rec_2202017,Human_Splice_Rec_2202026 RMVar_hsa_circ_104682,RMVar_hsa_circ_83911,RMVar_hsa_circ_262325,RMVar_hsa_circ_121263,RMVar_hsa_circ_262326,RMVar_hsa_circ_262327,RMVar_hsa_circ_119881,RMVar_hsa_circ_262328 98626 RMVar_ID_98626 Human_SNP_ID_716110479 m1A Human chrX + 47585317 47585317 47585317 ATACTTCCACAGGTCCCACAACCGCAGCGAGGAGTTTCTCATTGCTGGTGAGGCACCGTCCCCGC ATACTTCCACAGGTCCCACAACCGCAGCGAGGTGTTTCTCATTGCTGGTGAGGCACCGTCCCCGC A T TIMP1 Ensembl:ENSG00000102265 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:47583461..47585350 32194978 MeRIP-seq:(Medium) rs778571038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186477,Human_RBP_ID_798992,Human_RBP_ID_17672674,Human_RBP_ID_22777593 Human_Splice_Rec_2202011,Human_Splice_Rec_2202019 RMVar_hsa_circ_88884,RMVar_hsa_circ_83911,RMVar_hsa_circ_262325,RMVar_hsa_circ_121263,RMVar_hsa_circ_262327,RMVar_hsa_circ_119881,RMVar_hsa_circ_262328,RMVar_hsa_circ_262329,RMVar_hsa_circ_48888 98627 RMVar_ID_98627 Human_SNP_ID_716110803 m1A Human chrX - 47586689 47586689 47586689 GCAGGCTTCAGCTTCCACTCCGGGCAGGATTCAGGCTATCTGGGACCGCAGGGACTGCCAGGTGC GCAGGCTTCAGCTTCCACTCCGGGCAGGATTCGGGCTATCTGGGACCGCAGGGACTGCCAGGTGC T C SYN1,Z84466.1 Ensembl:ENSG00000008056,Ensembl:ENSG00000283743 Protein coding,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:47586639..47586739 32194978 MeRIP-seq:(Medium) rs1360544930 Functional Loss SNV dbSNP153 33..33 33 - - - 98628 RMVar_ID_98628 Human_SNP_ID_716110806 m1A Human chrX - 47586696 47586696 47586696 ACACTGTGCAGGCTTCAGCTTCCACTCCGGGCAGGATTCAGGCTATCTGGGACCGCAGGGACTGC ACACTGTGCAGGCTTCAGCTTCCACTCCGGGCGGGATTCAGGCTATCTGGGACCGCAGGGACTGC T C SYN1,Z84466.1 Ensembl:ENSG00000008056,Ensembl:ENSG00000283743 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47586651..47586775 32194978 MeRIP-seq:(Medium) rs201072961 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98629 RMVar_ID_98629 Human_SNP_ID_716119946 m1A Human chrX - 47637800 47637800 47637800 GACCCCAGGATCGGGAAGTGGCTCCGGCCTCCAGGCTCCGGGGCCGGCGCTGACCCCATCCCTGC GACCCCAGGATCGGGAAGTGGCTCCGGCCTCCCGGCTCCGGGGCCGGCGCTGACCCCATCCCTGC T G ELK1 Ensembl:ENSG00000126767 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:47637700..47637837 26863196 MeRIP-seq:(Medium) rs778401778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2202125 RMVar_hsa_circ_268466 98630 RMVar_ID_98630 Human_SNP_ID_716120632 m1A Human chrX + 47641474 47641474 47641474 CGCTGGGGGAGTGCTCACGCCATCCCAGGGGTACCTGGAGAGCAAACAGCTGAGTTGAGAGGCTG CGCTGGGGGAGTGCTCACGCCATCCCAGGGGTGCCTGGAGAGCAAACAGCTGAGTTGAGAGGCTG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:47641426..47641500 26863410 MeRIP-seq:(Medium) rs761411612 Functional Loss SNV dbSNP153 33..33 33 - - - 98631 RMVar_ID_98631 Human_SNP_ID_716121430 m1A Human chrX - 47646776 47646775 47646776 GCAGGTGATACATAGGATAGGATTGCAGGGGCAGGGGGAGAAGGATGACACACTAGCTAATAGCT GCAGGTGATACATAGGATAGGATTGCAGGGGC_GGGGGAGAAGGATGACACACTAGCTAATAGCT CT C ELK1 Ensembl:ENSG00000126767 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:47646772..47646900 26863196 MeRIP-seq:(Medium) rs924804049 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8006076 98632 RMVar_ID_98632 Human_SNP_ID_716123599 m1A Human chrX - 47658921 47658921 47658921 CCCTCCCCACTCCCCAGGAGCCCATCATGGCGACGCCCCCTAAGCGGCGGGCGGTGGAGGCCACG CCCTCCCCACTCCCCAGGAGCCCATCATGGCGGCGCCCCCTAAGCGGCGGGCGGTGGAGGCCACG T C UXT Ensembl:ENSG00000126756 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:47657776..47659175;chrX:47658780..47659175;chrX:47657801..47659175 26863196 MeRIP-seq:(Medium) rs773254620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735416,Human_RBP_ID_5076107,Human_RBP_ID_5124724,Human_RBP_ID_22467569 Human_Splice_Rec_2202150,Human_Splice_Rec_2202161,Human_Splice_Rec_2202162,Human_Splice_Rec_2202176,Human_Splice_Rec_2202185,Human_Splice_Rec_2202186 RMVar_hsa_circ_115002,RMVar_hsa_circ_262335 98633 RMVar_ID_98633 Human_SNP_ID_716123726 m1A Human chrX + 47659282 47659282 47659282 GGCCAAAGGGGAGAAGAGAAGGGCAGGGCTTCACGGAATCCGAGGAGATCAAAGAAGACTAGGGC GGCCAAAGGGGAGAAGAGAAGGGCAGGGCTTCTCGGAATCCGAGGAGATCAAAGAAGACTAGGGC A T UXT-AS1 Ensembl:ENSG00000267064 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:47659196..47659345 26863196 MeRIP-seq:(Medium) rs1260322814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932014 98634 RMVar_ID_98634 Human_SNP_ID_716269214 m1A Human chrX - 48468321 48468321 48468321 TGGCGCGGGGGACCGGGGAATGAAAGACACAGATGGCAAGAGAGACAGCGTGAGTCTGGGGTCTG TGGCGCGGGGGACCGGGGAATGAAAGACACAGCTGGCAAGAGAGACAGCGTGAGTCTGGGGTCTG T G SLC38A5 Ensembl:ENSG00000017483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48467701..48468425 26863196 MeRIP-seq:(Medium) rs1352459760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3976455 Human_Splice_Rec_2202728,Human_Splice_Rec_2202767 RMVar_hsa_circ_27917 98635 RMVar_ID_98635 Human_SNP_ID_716270717 m1A Human chrX - 48476848 48476848 48476848 TCAATACCTGGGGGATCATTTTCCCATCCATCACTCGTTATATTCTAGTTGCTTACTCTGCCATC TCAATACCTGGGGGATCATTTTCCCATCCATCGCTCGTTATATTCTAGTTGCTTACTCTGCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48476843..48477082 26863196 MeRIP-seq:(Medium) rs1306620555 Functional Loss SNV dbSNP153 33..33 33 - - - 98636 RMVar_ID_98636 Human_SNP_ID_716270917 m1A Human chrX + 48478053 48478053 48478053 CAGGTCCTTGAGCAACTGGTGTGTGAAATGGGACGGACGTCAAAGGACAAGCGGGATGTCTACTA CAGGTCCTTGAGCAACTGGTGTGTGAAATGGGGCGGACGTCAAAGGACAAGCGGGATGTCTACTA A G FTSJ1 Ensembl:ENSG00000068438 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48477923..48478309 26863196 MeRIP-seq:(Medium) rs1556966912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24343799,Human_RBP_ID_26834737 Human_Splice_Rec_2202866,Human_Splice_Rec_2202890,Human_Splice_Rec_2202908 98637 RMVar_ID_98637 Human_SNP_ID_716276764 m1A Human chrX - 48512635 48512635 48512635 GGCCCACGCAAGTGGACAGCACAAGGCACAGCAGGGCCAGTGCCAGGCTCCGGGCCACCTTCTGC GGCCCACGCAAGTGGACAGCACAAGGCACAGCGGGGCCAGTGCCAGGCTCCGGGCCACCTTCTGC T C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:48512355..48512635 32194978 MeRIP-seq:(Medium) rs782482532 Functional Loss SNV dbSNP153 33..33 33 - - - 98638 RMVar_ID_98638 Human_SNP_ID_716277151 m1A Human chrX - 48514564 48514564 48514564 TTCCAGCTTGTGACAACTTCCACCATTGACCGAGGCAGCTCCACATTCAGTGGCTTGGACACCGT TTCCAGCTTGTGACAACTTCCACCATTGACCGCGGCAGCTCCACATTCAGTGGCTTGGACACCGT T G RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:48512847..48514577 32194978 MeRIP-seq:(Medium) rs1556974825 Functional Loss SNV dbSNP153 33..33 33 - - - 98639 RMVar_ID_98639 Human_SNP_ID_716278674 m1A Human chrX - 48523716 48523711 48523717 TGTGTATAGGCAGGAAGTTAAAAAAAAAAAAAAAAAAGGAACAGAAAAACCTGGACAAATAGAAA TGTGTATAGGCAGGAAGTTAAAAAAAAAAAA______GGAACAGAAAAACCTGGACAAATAGAAA CTTTTTT C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chrX:48523676..48523725 26863196 MeRIP-seq:(Medium) rs782299900 Functional Loss DEL dbSNP153 32..37 33 - - - 98640 RMVar_ID_98640 Human_SNP_ID_716278675 m1A Human chrX - 48523716 48523711 48523717 TGTGTATAGGCAGGAAGTTAAAAAAAAAAAAAAAAAAGGAACAGAAAAACCTGGACAAATAGAAA TGTGTATAGGCAGGAAGTTAAAAAAAAAAAA__AAAAGGAACAGAAAAACCTGGACAAATAGAAA CTTTTTT CTTTT RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chrX:48523676..48523725 26863196 MeRIP-seq:(Medium) rs782299900 Functional Loss DEL dbSNP153 32..33 33 - - - 98641 RMVar_ID_98641 Human_SNP_ID_716278706 m1A Human chrX + 48523767 48523765 48523767 CCTGCCTATACACACGCAGCCATCAGCCCACAAAGACATGACTACCAACGCGGGCCCCTTGCACC CCTGCCTATACACACGCAGCCATCAGCCCAC__AGACATGACTACCAACGCGGGCCCCTTGCACC CAA C AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:48523751..48523775 26863196 MeRIP-seq:(Medium) rs1193600623 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_800297,Human_RBP_ID_1715581,Human_RBP_ID_5076579,Human_RBP_ID_16898672,Human_RBP_ID_17442710,Human_RBP_ID_22467927,Human_RBP_ID_23216855,Human_RBP_ID_24445233 Human_Splice_Rec_2203212,Human_Splice_Rec_2203220,Human_Splice_Rec_2203230,Human_Splice_Rec_2203240,Human_Splice_Rec_2203248 98642 RMVar_ID_98642 Human_SNP_ID_716278709 m1A Human chrX + 48523782 48523782 48523782 GCAGCCATCAGCCCACAAAGACATGACTACCAACGCGGGCCCCTTGCACCCATACTGGCCTCAGC GCAGCCATCAGCCCACAAAGACATGACTACCACCGCGGGCCCCTTGCACCCATACTGGCCTCAGC A C AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48523676..48524015 26863196 MeRIP-seq:(Medium) rs1556977003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258050,Human_RBP_ID_800297,Human_RBP_ID_1715581,Human_RBP_ID_5076579,Human_RBP_ID_8006482,Human_RBP_ID_8719638,Human_RBP_ID_16898672,Human_RBP_ID_17442710,Human_RBP_ID_22467927,Human_RBP_ID_24445233,Human_RBP_ID_24526923,Human_RBP_ID_26571803,Human_RBP_ID_27382477 Human_Splice_Rec_2203212,Human_Splice_Rec_2203220,Human_Splice_Rec_2203230,Human_Splice_Rec_2203240,Human_Splice_Rec_2203248 98643 RMVar_ID_98643 Human_SNP_ID_716278710 m1A Human chrX + 48523782 48523782 48523782 GCAGCCATCAGCCCACAAAGACATGACTACCAACGCGGGCCCCTTGCACCCATACTGGCCTCAGC GCAGCCATCAGCCCACAAAGACATGACTACCAGCGCGGGCCCCTTGCACCCATACTGGCCTCAGC A G AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48523676..48524015 26863196 MeRIP-seq:(Medium) rs1556977003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258050,Human_RBP_ID_800297,Human_RBP_ID_1715581,Human_RBP_ID_5076579,Human_RBP_ID_8006482,Human_RBP_ID_8719638,Human_RBP_ID_16898672,Human_RBP_ID_17442710,Human_RBP_ID_22467927,Human_RBP_ID_24445233,Human_RBP_ID_24526923,Human_RBP_ID_26571803,Human_RBP_ID_27382477 Human_Splice_Rec_2203212,Human_Splice_Rec_2203220,Human_Splice_Rec_2203230,Human_Splice_Rec_2203240,Human_Splice_Rec_2203248 98644 RMVar_ID_98644 Human_SNP_ID_716279282 m1A Human chrX - 48526977 48526977 48526977 CTCCCTTGGCATACTCTTTCCCTGAAGAAAAGAAGAGAGAGATATGAAGAATAAAGGCAGTGAAA CTCCCTTGGCATACTCTTTCCCTGAAGAAAAGGAGAGAGAGATATGAAGAATAAAGGCAGTGAAA T C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:48526976..48527025 32194978 MeRIP-seq:(Medium) rs181299601 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98645 RMVar_ID_98645 Human_SNP_ID_716284201 m1A Human chrX + 48554977 48554977 48554977 GGGAGAGATTGGAGAGGAATACAGAGGAAGTGAGGACTGGTTAGGAGGCAGTTTCAGGTGAGAGA GGGAGAGATTGGAGAGGAATACAGAGGAAGTGGGGACTGGTTAGGAGGCAGTTTCAGGTGAGAGA A G TBC1D25 Ensembl:ENSG00000068354 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48554973..48555106 26863196 MeRIP-seq:(Medium) rs193271427 Functional Loss SNV dbSNP153 33..33 33 - - - 98646 RMVar_ID_98646 Human_SNP_ID_716288099 m1A Human chrX - 48575225 48575225 48575225 AAGTGGTCTTCCAGTGCCTGCTCGTCGGTGTTAAAGTTGAGCCCTCCCACGAAGAGCTTTCCTTC AAGTGGTCTTCCAGTGCCTGCTCGTCGGTGTTTAAGTTGAGCCCTCCCACGAAGAGCTTTCCTTC T A RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48575151..48575225 26863196 MeRIP-seq:(Medium) rs371016165 Functional Loss SNV dbSNP153 33..33 33 - - - 98647 RMVar_ID_98647 Human_SNP_ID_716288100 m1A Human chrX - 48575225 48575225 48575225 AAGTGGTCTTCCAGTGCCTGCTCGTCGGTGTTAAAGTTGAGCCCTCCCACGAAGAGCTTTCCTTC AAGTGGTCTTCCAGTGCCTGCTCGTCGGTGTTGAAGTTGAGCCCTCCCACGAAGAGCTTTCCTTC T C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48575151..48575225 26863196 MeRIP-seq:(Medium) rs371016165 Functional Loss SNV dbSNP153 33..33 33 - - - 98648 RMVar_ID_98648 Human_SNP_ID_716288425 m1A Human chrX - 48576540 48576540 48576540 ATATCCATACCCTCCAGGTCGACTGTCATAATACCTGCCACTCCCATAGCCCTGGTCCCCACCAC ATATCCATACCCTCCAGGTCGACTGTCATAATCCCTGCCACTCCCATAGCCCTGGTCCCCACCAC T G RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48576401..48576646 26863196 MeRIP-seq:(Medium) rs200342072 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98649 RMVar_ID_98649 Human_SNP_ID_716288426 m1A Human chrX + 48576541 48576541 48576541 TGGTGGGGACCAGGGCTATGGGAGTGGCAGGTATTATGACAGTCGACCTGGAGGGTATGGATATG TGGTGGGGACCAGGGCTATGGGAGTGGCAGGTGTTATGACAGTCGACCTGGAGGGTATGGATATG A G RBM3 Ensembl:ENSG00000102317 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48576309..48576606 26863196 MeRIP-seq:(Medium) rs782223203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93597,Human_RBP_ID_257288,Human_RBP_ID_735551,Human_RBP_ID_969085,Human_RBP_ID_1715621,Human_RBP_ID_2075233,Human_RBP_ID_3977263,Human_RBP_ID_5065396,Human_RBP_ID_5232147,Human_RBP_ID_5410855,Human_RBP_ID_8006584,Human_RBP_ID_8719678,Human_RBP_ID_9352229,Human_RBP_ID_16898931,Human_RBP_ID_18151525,Human_RBP_ID_19026611,Human_RBP_ID_22468327,Human_RBP_ID_22519596,Human_RBP_ID_22841573,Human_RBP_ID_23142582,Human_RBP_ID_26300883,Human_RBP_ID_26571824,Human_RBP_ID_27148724,Human_RBP_ID_27382525,Human_RBP_ID_27844006 Human_Splice_Rec_2203305,Human_Splice_Rec_2203319,Human_Splice_Rec_2203320,Human_Splice_Rec_2203333,Human_Splice_Rec_2203334,Human_Splice_Rec_2203347,Human_Splice_Rec_2203355,Human_Splice_Rec_2203356,Human_Splice_Rec_2203369,Human_Splice_Rec_2203370,Human_Splice_Rec_2203377,Human_Splice_Rec_2203378 Human_miRNA_ID_2508338,Human_miRNA_ID_2585689 RMVar_hsa_circ_60709,RMVar_hsa_circ_301042,RMVar_hsa_circ_85851,RMVar_hsa_circ_262370,RMVar_hsa_circ_262371,RMVar_hsa_circ_96073,RMVar_hsa_circ_262372,RMVar_hsa_circ_124293,RMVar_hsa_circ_349521,RMVar_hsa_circ_262373 98650 RMVar_ID_98650 Human_SNP_ID_716288436 m1A Human chrX + 48576569 48576563 48576569 AGGTATTATGACAGTCGACCTGGAGGGTATGGATATGGATATGGACGTTCCAGAGACTATAATGG AGGTATTATGACAGTCGACCTGGAGGG______TATGGATATGGACGTTCCAGAGACTATAATGG GTATGGA G RBM3 Ensembl:ENSG00000102317 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1569485634 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_93597,Human_RBP_ID_735552,Human_RBP_ID_1062663,Human_RBP_ID_1230782,Human_RBP_ID_1715622,Human_RBP_ID_2075234,Human_RBP_ID_3923721,Human_RBP_ID_3977263,Human_RBP_ID_5065396,Human_RBP_ID_5410855,Human_RBP_ID_8006584,Human_RBP_ID_8719679,Human_RBP_ID_8935886,Human_RBP_ID_16898932,Human_RBP_ID_17718397,Human_RBP_ID_18151525,Human_RBP_ID_19026611,Human_RBP_ID_22468748,Human_RBP_ID_22841573,Human_RBP_ID_23108658,Human_RBP_ID_24343880,Human_RBP_ID_27793747 Human_Splice_Rec_2203305,Human_Splice_Rec_2203319,Human_Splice_Rec_2203320,Human_Splice_Rec_2203333,Human_Splice_Rec_2203334,Human_Splice_Rec_2203347,Human_Splice_Rec_2203355,Human_Splice_Rec_2203356,Human_Splice_Rec_2203369,Human_Splice_Rec_2203370,Human_Splice_Rec_2203377,Human_Splice_Rec_2203378 RMVar_hsa_circ_60709,RMVar_hsa_circ_301042,RMVar_hsa_circ_85851,RMVar_hsa_circ_262370,RMVar_hsa_circ_262371,RMVar_hsa_circ_96073,RMVar_hsa_circ_262372,RMVar_hsa_circ_124293,RMVar_hsa_circ_349521,RMVar_hsa_circ_262373 98651 RMVar_ID_98651 Human_SNP_ID_716288745 m1A Human chrX - 48577525 48577524 48577525 ATAAAATAAGATGCTTCGGTGCAGCTCCAAAAACCTTTATAAATACAGCCATTTGGAAGGACGAT ATAAAATAAGATGCTTCGGTGCAGCTCCAAAA_CCTTTATAAATACAGCCATTTGGAAGGACGAT GT G RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:48577474..48577574 32194978 MeRIP-seq:(Medium) rs1556989641 Functional Loss DEL dbSNP153 33..33 33 - - - 98652 RMVar_ID_98652 Human_SNP_ID_716292604 m1A Human chrX - 48597569 48597569 48597569 TCCGGTTCTTGAGGCCCCCCGGAGCGGCCCTGAGACCACTGTCGCCGGTTCCTTCTGTCTCTCCT TCCGGTTCTTGAGGCCCCCCGGAGCGGCCCTGCGACCACTGTCGCCGGTTCCTTCTGTCTCTCCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:48597501..48597681 26863196 MeRIP-seq:(Medium) rs1457796593 Functional Loss SNV dbSNP153 33..33 33 - - - 98653 RMVar_ID_98653 Human_SNP_ID_716292651 m1A Human chrX - 48597842 48597842 48597842 ACATCGAGTCCCTCCGCGCCGGAGATGTCACGAACTCCCCCCCGGGTGTTACCATGGTCATCACC ACATCGAGTCCCTCCGCGCCGGAGATGTCACGGACTCCCCCCCGGGTGTTACCATGGTCATCACC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:48597826..48598000 26863196 MeRIP-seq:(Medium) rs1238523496 Functional Loss SNV dbSNP153 33..33 33 - - - 98654 RMVar_ID_98654 Human_SNP_ID_716292652 m1A Human chrX - 48597845 48597845 48597845 TAGACATCGAGTCCCTCCGCGCCGGAGATGTCACGAACTCCCCCCCGGGTGTTACCATGGTCATC TAGACATCGAGTCCCTCCGCGCCGGAGATGTCCCGAACTCCCCCCCGGGTGTTACCATGGTCATC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:48597830..48597980 32194978 MeRIP-seq:(Medium) rs1376268264 Functional Loss SNV dbSNP153 33..33 33 - - - 98655 RMVar_ID_98655 Human_SNP_ID_716292796 m1A Human chrX - 48598430 48598430 48598430 TGACTGGGTCAGCGCAGACAATAATTAGGGTCAGTATACCAGGGCGACAGAAATCAGACTGACAT TGACTGGGTCAGCGCAGACAATAATTAGGGTCCGTATACCAGGGCGACAGAAATCAGACTGACAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48598428..48598629 26863196 MeRIP-seq:(Medium) rs1159800984 Functional Loss SNV dbSNP153 33..33 33 - - - 98656 RMVar_ID_98656 Human_SNP_ID_716292807 m1A Human chrX - 48598530 48598530 48598530 CCTGTGGTGGGAGTGAGTCTGCAGTAATAATGAGCATGGTCATGAGGTCAGTTTGCAGACAACAG CCTGTGGTGGGAGTGAGTCTGCAGTAATAATGCGCATGGTCATGAGGTCAGTTTGCAGACAACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48598528..48598831 26863196 MeRIP-seq:(Medium) rs1286388350 Functional Loss SNV dbSNP153 33..33 33 - - - 98657 RMVar_ID_98657 Human_SNP_ID_716293651 m1A Human chrX - 48602054 48602052 48602055 CGCTTGGCTTTGGTCAGCTTCCCTGCAGCAGCAGAGGGAGGGAAGGCAAAGGTGAGGGTGAGGGC CGCTTGGCTTTGGTCAGCTTCCCTGCAGCAG___AGGGAGGGAAGGCAAAGGTGAGGGTGAGGGC TCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48602051..48602100 26863196 MeRIP-seq:(Medium) rs1330113426 Functional Loss DEL dbSNP153 32..34 33 - - - 98658 RMVar_ID_98658 Human_SNP_ID_716314027 m1A Human chrX - 48708855 48708853 48708856 CAGACAGACACATAGATCTGGCATCTGATAGCAGGGCATACAGTCTCATGTAGGGGCACTCTGGG CAGACAGACACATAGATCTGGCATCTGATAG___GGCATACAGTCTCATGTAGGGGCACTCTGGG CCTG C AC231533.1 Ensembl:ENSG00000232828 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48708805..48708889 26863196 MeRIP-seq:(Medium) rs782419043 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_16899457 98659 RMVar_ID_98659 Human_SNP_ID_716314041 m1A Human chrX - 48708888 48708885 48708889 AGGTTAGTCTGGGGGGCCGGCGGGATGGACACACAGACAGACACATAGATCTGGCATCTGATAGC AGGTTAGTCTGGGGGGCCGGCGGGATGGACA____GACAGACACATAGATCTGGCATCTGATAGC CTGTG C AC231533.1 Ensembl:ENSG00000232828 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48708853..48708945 26863196 MeRIP-seq:(Medium) rs1557010601 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_8006790 98660 RMVar_ID_98660 Human_SNP_ID_716330571 m1A Human chrX - 48802225 48802225 48802225 ATCTCCCGGGATAATCACCCACCCTTTCACTCAGCCGGCCCCGGCCCCGACCCCGGTTTCGACTC ATCTCCCGGGATAATCACCCACCCTTTCACTCGGCCGGCCCCGGCCCCGACCCCGGTTTCGACTC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48802042..48802307 26863196 MeRIP-seq:(Medium) rs1557022560 Functional Loss SNV dbSNP153 33..33 33 - - - 98661 RMVar_ID_98661 Human_SNP_ID_716334341 m1A Human chrX - 48823282 48823282 48823282 CCAACAGCATCCTCTGAGGTGGTCTGGTCCAGAATGGCTCCTCCCACAGTCTCCTCTGAGGTGGT CCAACAGCATCCTCTGAGGTGGTCTGGTCCAGTATGGCTCCTCCCACAGTCTCCTCTGAGGTGGT T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48823234..48823476 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - RMVar_hsa_circ_78757,RMVar_hsa_circ_262392 98662 RMVar_ID_98662 Human_SNP_ID_716336028 m1A Human chrX - 48831443 48831443 48831443 CTTTGCGCTCGGCCCTGCAGGTACTTGCTGGGACGGATTCTTGCGGGAAGCGCGGACTCCGAGGG CTTTGCGCTCGGCCCTGCAGGTACTTGCTGGGGCGGATTCTTGCGGGAAGCGCGGACTCCGAGGG T C PCSK1N Ensembl:ENSG00000102109 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:48831142..48834556 32194978 MeRIP-seq:(Medium) rs782523513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735729,Human_RBP_ID_5124604,Human_RBP_ID_17667264,Human_RBP_ID_22778144 Human_Splice_Rec_2204381 98663 RMVar_ID_98663 Human_SNP_ID_716336880 m1A Human chrX + 48835523 48835523 48835523 GCCCCCGGCCCGCGGCCCCCAGAGCAGCGGCGACCCCGCCATGCTGCCCCAGCGAGCCGGGCTCC GCCCCCGGCCCGCGGCCCCCAGAGCAGCGGCGCCCCCGCCATGCTGCCCCAGCGAGCCGGGCTCC A C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:48835426..48835600 26863410 MeRIP-seq:(Medium) rs1557034052 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98664 RMVar_ID_98664 Human_SNP_ID_716336881 m1A Human chrX + 48835523 48835523 48835523 GCCCCCGGCCCGCGGCCCCCAGAGCAGCGGCGACCCCGCCATGCTGCCCCAGCGAGCCGGGCTCC GCCCCCGGCCCGCGGCCCCCAGAGCAGCGGCGGCCCCGCCATGCTGCCCCAGCGAGCCGGGCTCC A G RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:48835426..48835600 26863410 MeRIP-seq:(Medium) rs1557034052 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98665 RMVar_ID_98665 Human_SNP_ID_716348175 m1A Human chrX + 48897995 48897994 48897996 GTTGAGAGAAGGTCTCATTCGGTGTTTTGGGAAGAGAGTCGTGTGGGCCCAGGTATCGTAGCGGC GTTGAGAGAAGGTCTCATTCGGTGTTTTGGGA__AGAGTCGTGTGGGCCCAGGTATCGTAGCGGC AAG A PQBP1 Ensembl:ENSG00000102103 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48897799..48898374 26863196 MeRIP-seq:(Medium) rs1322947236 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1715740,Human_RBP_ID_2075289,Human_RBP_ID_5082876,Human_RBP_ID_5432194,Human_RBP_ID_8719775,Human_RBP_ID_18454433 Human_Splice_Rec_2204386,Human_Splice_Rec_2204398,Human_Splice_Rec_2204407,Human_Splice_Rec_2204419,Human_Splice_Rec_2204441,Human_Splice_Rec_2204451,Human_Splice_Rec_2204465,Human_Splice_Rec_2204477,Human_Splice_Rec_2204489 98666 RMVar_ID_98666 Human_SNP_ID_716348184 m1A Human chrX - 48898059 48898059 48898059 CAACGTTACCAATACACTCGTGCAGGTAGTGGAAGGCTGTCACACCGCCCGTCTCTCTCGTGTCG CAACGTTACCAATACACTCGTGCAGGTAGTGGTAGGCTGTCACACCGCCCGTCTCTCTCGTGTCG T A TIMM17B Ensembl:ENSG00000126768 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:48898009..48898107 32194978 MeRIP-seq:(Medium) rs1332655051 Functional Loss SNV dbSNP153 33..33 33 - - - 98667 RMVar_ID_98667 Human_SNP_ID_716348228 m1A Human chrX + 48898256 48898256 48898256 TTCTTAGGCTGTGGGCGGAGCCTGGGCCTGGGAGAGGAACAGGGCCCTGGAGCACCTGGTTTCGG TTCTTAGGCTGTGGGCGGAGCCTGGGCCTGGGTGAGGAACAGGGCCCTGGAGCACCTGGTTTCGG A T PQBP1 Ensembl:ENSG00000102103 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48898252..48898332 26863196 MeRIP-seq:(Medium) rs1483631963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3258344,Human_RBP_ID_5412250 Human_Splice_Rec_2204511,Human_Splice_Rec_2204523,Human_Splice_Rec_2204533 98668 RMVar_ID_98668 Human_SNP_ID_716349112 m1A Human chrX + 48902506 48902483 48902506 CCATCGCCGGGAGGAGCTGGCTCCCTATCCCAAGAGCAAGAAGGGTAAGCTGGGCAGAATGGGGC CCATCGCCGG_______________________GAGCAAGAAGGGTAAGCTGGGCAGAATGGGGC GGAGGAGCTGGCTCCCTATCCCAA G PQBP1 Ensembl:ENSG00000102103 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:48902362..48902558 32194978 MeRIP-seq:(Medium) rs606231197 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_800448,Human_RBP_ID_17718415,Human_RBP_ID_18151667 Human_Splice_Rec_2204394,Human_Splice_Rec_2204415,Human_Splice_Rec_2204427,Human_Splice_Rec_2204437,Human_Splice_Rec_2204473,Human_Splice_Rec_2204497,Human_Splice_Rec_2204507,Human_Splice_Rec_2204519,Human_Splice_Rec_2204531,Human_Splice_Rec_2204561 Clinvar_Rec_605 RMVar_hsa_circ_27187 98669 RMVar_ID_98669 Human_SNP_ID_716349572 m1A Human chrX - 48904702 48904698 48904702 TGAAGTGAGGGCTGGCAGCAATGGGGGGACACAAGGGAGGGGGACTGGGGTGGAGGGTGTTGGGC TGAAGTGAGGGCTGGCAGCAATGGGGGGACAC____GAGGGGGACTGGGGTGGAGGGTGTTGGGC CCCTT C SLC35A2 Ensembl:ENSG00000102100 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48904651..48904725 26863196 MeRIP-seq:(Medium) rs56243326 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8006928,Human_RBP_ID_8227019,Human_RBP_ID_18151688,Human_RBP_ID_27552228 RMVar_hsa_circ_110044,RMVar_hsa_circ_108589,RMVar_hsa_circ_262398,RMVar_hsa_circ_262399,RMVar_hsa_circ_82648,RMVar_hsa_circ_262400 98670 RMVar_ID_98670 Human_SNP_ID_716349946 m1A Human chrX - 48906513 48906513 48906513 AGGTAACGTGAAGCACCTGGTTCTCTTCCTCCATGAGGCTGTCCTGGTGCAGTATGTGGACACGC AGGTAACGTGAAGCACCTGGTTCTCTTCCTCCGTGAGGCTGTCCTGGTGCAGTATGTGGACACGC T C SLC35A2 Ensembl:ENSG00000102100 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:48906400..48909821 32194978 MeRIP-seq:(Medium) rs1557043147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1062738,Human_RBP_ID_21833354,Human_RBP_ID_27571195 Human_Splice_Rec_2204650,Human_Splice_Rec_2204658,Human_Splice_Rec_2204666,Human_Splice_Rec_2204672,Human_Splice_Rec_2204680,Human_Splice_Rec_2204686,Human_Splice_Rec_2204692,Human_Splice_Rec_2204696,Human_Splice_Rec_2204705,Human_Splice_Rec_2204711,Human_Splice_Rec_2204719,Human_Splice_Rec_2204725,Human_Splice_Rec_2204731,Human_Splice_Rec_2204743,Human_Splice_Rec_2204747,Human_Splice_Rec_2204749 Human_miRNA_ID_2627978,Human_miRNA_ID_2748814,Human_miRNA_ID_3079132 RMVar_hsa_circ_43431,RMVar_hsa_circ_110044,RMVar_hsa_circ_108589,RMVar_hsa_circ_262398,RMVar_hsa_circ_262399 98671 RMVar_ID_98671 Human_SNP_ID_716350887 m1A Human chrX - 48911609 48911609 48911609 CCAACATGGCAGCGGTTGGGGCTGGTGGTTCCACCGCGGCGCCCGGGCCAGGGGCGGTTTCCGCG CCAACATGGCAGCGGTTGGGGCTGGTGGTTCCGCCGCGGCGCCCGGGCCAGGGGCGGTTTCCGCG T C SLC35A2 Ensembl:ENSG00000102100 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:48911485..48911610;chrX:48911480..48911608 26863196 MeRIP-seq:(Medium) rs1054898966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799282,Human_RBP_ID_966674,Human_RBP_ID_5075819,Human_RBP_ID_18151695,Human_RBP_ID_22467944,Human_RBP_ID_24344441 Human_Splice_Rec_2204647,Human_Splice_Rec_2204655,Human_Splice_Rec_2204663,Human_Splice_Rec_2204669,Human_Splice_Rec_2204683,Human_Splice_Rec_2204689,Human_Splice_Rec_2204704,Human_Splice_Rec_2204714,Human_Splice_Rec_2204728,Human_Splice_Rec_2204734,Human_Splice_Rec_2204744,Human_Splice_Rec_2204748 RMVar_hsa_circ_108589,RMVar_hsa_circ_262399 98672 RMVar_ID_98672 Human_SNP_ID_716350888 m1A Human chrX - 48911609 48911609 48911609 CCAACATGGCAGCGGTTGGGGCTGGTGGTTCCACCGCGGCGCCCGGGCCAGGGGCGGTTTCCGCG CCAACATGGCAGCGGTTGGGGCTGGTGGTTCCCCCGCGGCGCCCGGGCCAGGGGCGGTTTCCGCG T G SLC35A2 Ensembl:ENSG00000102100 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:48911485..48911610;chrX:48911480..48911608 26863196 MeRIP-seq:(Medium) rs1054898966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799282,Human_RBP_ID_966674,Human_RBP_ID_5075819,Human_RBP_ID_18151695,Human_RBP_ID_22467944,Human_RBP_ID_24344441 Human_Splice_Rec_2204647,Human_Splice_Rec_2204655,Human_Splice_Rec_2204663,Human_Splice_Rec_2204669,Human_Splice_Rec_2204683,Human_Splice_Rec_2204689,Human_Splice_Rec_2204704,Human_Splice_Rec_2204714,Human_Splice_Rec_2204728,Human_Splice_Rec_2204734,Human_Splice_Rec_2204744,Human_Splice_Rec_2204748 RMVar_hsa_circ_108589,RMVar_hsa_circ_262399 98673 RMVar_ID_98673 Human_SNP_ID_716352528 m1A Human chrX - 48918873 48918873 48918873 CGCTGCCCCGGGCGTCCACGCCCTGCGGGCTTAGCGGGTTCAGTGGGCTCAATCTGCGCAGCGCC CGCTGCCCCGGGCGTCCACGCCCTGCGGGCTTGGCGGGTTCAGTGGGCTCAATCTGCGCAGCGCC T C PIM2 Ensembl:ENSG00000102096 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:48918599..48918925 32194978 MeRIP-seq:(Medium) rs782507557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5065964,Human_RBP_ID_18151714 Human_Splice_Rec_2204750 RMVar_hsa_circ_262402,RMVar_hsa_circ_91620 98674 RMVar_ID_98674 Human_SNP_ID_716352532 m1A Human chrX + 48918882 48918882 48918882 CAGATTGAGCCCACTGAACCCGCTAAGCCCGCAGGGCGTGGACGCCCGGGGCAGCGCAGCTGGGG CAGATTGAGCCCACTGAACCCGCTAAGCCCGCGGGGCGTGGACGCCCGGGGCAGCGCAGCTGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48918833..48918963 26863196 MeRIP-seq:(Medium) rs919033287 Functional Loss SNV dbSNP153 33..33 33 - - - 98675 RMVar_ID_98675 Human_SNP_ID_716353402 m1A Human chrX - 48922826 48922825 48922827 AACTGGCAGCCAGGCAGCCCCAGAGGAGAGAGACATTCAGACAGAGGAAAGTCTCCCTGCCCCTC AACTGGCAGCCAGGCAGCCCCAGAGGAGAGA__CATTCAGACAGAGGAAAGTCTCCCTGCCCCTC GTC G OTUD5 Ensembl:ENSG00000068308 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48922776..48923249 26863196 MeRIP-seq:(Medium) rs1289994067 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9247489,Human_RBP_ID_26574152,Human_RBP_ID_27552255 Human_Splice_Rec_2204781,Human_Splice_Rec_2204799 RMVar_hsa_circ_80320,RMVar_hsa_circ_262403 98676 RMVar_ID_98676 Human_SNP_ID_716353656 m1A Human chrX + 48923977 48923977 48923977 AGGTGACGAGGCTGAACTCCGCTGCCGCGGGGACCGGCTAGTCCACTCCTCCAGGCCACTGGAGG AGGTGACGAGGCTGAACTCCGCTGCCGCGGGGTCCGGCTAGTCCACTCCTCCAGGCCACTGGAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48923824..48923997 26863196 MeRIP-seq:(Medium) rs1557047084 Functional Loss SNV dbSNP153 33..33 33 - - - 98677 RMVar_ID_98677 Human_SNP_ID_716355660 m1A Human chrX - 48934867 48934867 48934867 CACAGACCTTAACCTTCCAATCTATTCTGCAGATGAAGAATGCCGACTACTTCTCCAACTATGTC CACAGACCTTAACCTTCCAATCTATTCTGCAGTTGAAGAATGCCGACTACTTCTCCAACTATGTC T A OTUD5 Ensembl:ENSG00000068308 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chrX:48934840..48934956;chrX:48934826..48935000 26863196 MeRIP-seq:(Medium) rs782207044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5410875,Human_RBP_ID_26363746,Human_RBP_ID_27844154 Human_Splice_Rec_2204769,Human_Splice_Rec_2204787,Human_Splice_Rec_2204805,Human_Splice_Rec_2204821,Human_Splice_Rec_2204837,Human_Splice_Rec_2204853,Human_Splice_Rec_2204869,Human_Splice_Rec_2204875 RMVar_hsa_circ_82088,RMVar_hsa_circ_291233,RMVar_hsa_circ_346111,RMVar_hsa_circ_41171,RMVar_hsa_circ_262407,RMVar_hsa_circ_262408 98678 RMVar_ID_98678 Human_SNP_ID_716355678 m1A Human chrX + 48934957 48934957 48934957 CCCTTCCCCAAAGGCCTCCATTTTCTCACCAGATAGTCCATGCAATGCTTTCGCACAACCTCATG CCCTTCCCCAAAGGCCTCCATTTTCTCACCAGGTAGTCCATGCAATGCTTTCGCACAACCTCATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48934951..48935025 26863196 MeRIP-seq:(Medium) rs1464624234 Functional Loss SNV dbSNP153 33..33 33 - - - 98679 RMVar_ID_98679 Human_SNP_ID_716357387 m1A Human chrX - 48944222 48944222 48944222 AGACAAGAAGGGCTTCATCATCAAGCAGATGAAGGAGGATGGCGCCTGTCTCTTCCGGGCTGTAG AGACAAGAAGGGCTTCATCATCAAGCAGATGAGGGAGGATGGCGCCTGTCTCTTCCGGGCTGTAG T C OTUD5 Ensembl:ENSG00000068308 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48944201..48944225 26863196 MeRIP-seq:(Medium) rs782206772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3923863,Human_RBP_ID_8007047 Human_Splice_Rec_2204765,Human_Splice_Rec_2204766,Human_Splice_Rec_2204783,Human_Splice_Rec_2204784,Human_Splice_Rec_2204801,Human_Splice_Rec_2204802,Human_Splice_Rec_2204817,Human_Splice_Rec_2204818,Human_Splice_Rec_2204833,Human_Splice_Rec_2204834,Human_Splice_Rec_2204849,Human_Splice_Rec_2204850,Human_Splice_Rec_2204864 RMVar_hsa_circ_291233,RMVar_hsa_circ_262409,RMVar_hsa_circ_112599 98680 RMVar_ID_98680 Human_SNP_ID_716360075 m1A Human chrX + 48957175 48957175 48957175 CAGCAGCCGCCCACGCCTACGGCACCACCCACACCCACCACCACGCCCGCGGCACCCACACCCGC CAGCAGCCGCCCACGCCTACGGCACCACCCACCCCCACCACCACGCCCGCGGCACCCACACCCGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:48956976..48957250 26863196 MeRIP-seq:(Medium) rs1557055681 Functional Loss SNV dbSNP153 33..33 33 - - - 98681 RMVar_ID_98681 Human_SNP_ID_716360092 m1A Human chrX - 48957214 48957211 48957214 CCCGGCGGCGGTCCCGGCGACGCGCTGGGCGCAGCGGCGGCGGGTGTGGGTGCCGCGGGCGTGGT CCCGGCGGCGGTCCCGGCGACGCGCTGGGCGC___GGCGGCGGGTGTGGGTGCCGCGGGCGTGGT CGCT C OTUD5 Ensembl:ENSG00000068308 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:48957113..48957326 26863196 MeRIP-seq:(Medium) rs781987271 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5244915,Human_RBP_ID_5330707,Human_RBP_ID_21997266 98682 RMVar_ID_98682 Human_SNP_ID_716360266 m1A Human chrX + 48957728 48957716 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTC____________GGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC CGGCGGCGGAGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs1465073395 Functional Loss DEL dbSNP153 22..33 33 - - - 98683 RMVar_ID_98683 Human_SNP_ID_716360268 m1A Human chrX + 48957728 48957719 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTCGGC_________GGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC CGGCGGAGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs1177851186 Functional Loss DEL dbSNP153 25..33 33 - - - 98684 RMVar_ID_98684 Human_SNP_ID_716360272 m1A Human chrX + 48957728 48957722 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTCGGCGGC______GGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC CGGAGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs781836892 Functional Loss DEL dbSNP153 28..33 33 - - - 98685 RMVar_ID_98685 Human_SNP_ID_716360273 m1A Human chrX + 48957728 48957722 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTCGGCGGCGGA___GGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC CGGAGGA CGGA - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs781836892 Functional Loss DEL dbSNP153 31..33 33 - - - 98686 RMVar_ID_98686 Human_SNP_ID_716360301 m1A Human chrX + 48957728 48957728 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs182033453 Functional Loss SNV dbSNP153 33..33 33 - - - 98687 RMVar_ID_98687 Human_SNP_ID_716360302 m1A Human chrX + 48957728 48957728 48957728 GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC GGCACCGGTTCGAGAACCCTCGGCGGCGGAGGTGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48957690..48957840 26863196 MeRIP-seq:(Medium) rs182033453 Functional Loss SNV dbSNP153 33..33 33 - - - 98688 RMVar_ID_98688 Human_SNP_ID_716360480 m1A Human chrX + 48958312 48958312 48958312 GACAGGAAAAACACCTCCCCTCCAGGATTCCAACTTGAACGCTGTCAGCCGGAATGACTGGAAAA GACAGGAAAAACACCTCCCCTCCAGGATTCCAGCTTGAACGCTGTCAGCCGGAATGACTGGAAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48957967..48958349 26863196 MeRIP-seq:(Medium) rs1192651271 Functional Loss SNV dbSNP153 33..33 33 - - - 98689 RMVar_ID_98689 Human_SNP_ID_716363108 m1A Human chrX - 48973110 48973110 48973110 TGGAGCTATGTATGGACAGAGATGGGCAGAGGATGTCACCCTGCATGTGTTCCGGGTGGGAAGAG TGGAGCTATGTATGGACAGAGATGGGCAGAGGGTGTCACCCTGCATGTGTTCCGGGTGGGAAGAG T C RF00017-4575,RF00017-4520 RNACentral:URS0000918622,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:48973069..48973179 26863196 MeRIP-seq:(Medium) rs1304710765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16900711,Human_RBP_ID_24344641 98690 RMVar_ID_98690 Human_SNP_ID_716365158 m1A Human chrX + 48983781 48983781 48983781 TCCCTTCAACCCTCATGTTCCCCTACCTTCCGAGCCTCCTGTAATTCCTGGGTCAACTGCTCCTT TCCCTTCAACCCTCATGTTCCCCTACCTTCCGGGCCTCCTGTAATTCCTGGGTCAACTGCTCCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:48983776..48983875;chrX:48983776..48983850 26863196 MeRIP-seq:(Medium) rs374247614 Functional Loss SNV dbSNP153 33..33 33 - - - 98691 RMVar_ID_98691 Human_SNP_ID_716366966 m1A Human chrX + 48993522 48993522 48993522 AGGGGCCCAGCTTGGGCAACCCCTGCTCCTGCAGCCCCCTCCTTCAGTTGCTGGTTCTCTTGCTC AGGGGCCCAGCTTGGGCAACCCCTGCTCCTGCGGCCCCCTCCTTCAGTTGCTGGTTCTCTTGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48993473..48993610 26863196 MeRIP-seq:(Medium) rs1557066075 Functional Loss SNV dbSNP153 33..33 33 - - - 98692 RMVar_ID_98692 Human_SNP_ID_716367998 m1A Human chrX - 48999660 48999660 48999660 GGAAAAGGTGAGCCAGGGTCTGAGGGCCTGGAAGGTCACTTTGGGTGTAGCACATACAGGTCTTA GGAAAAGGTGAGCCAGGGTCTGAGGGCCTGGAGGGTCACTTTGGGTGTAGCACATACAGGTCTTA T C GRIPAP1 Ensembl:ENSG00000068400 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48999657..48999755 26863196 MeRIP-seq:(Medium) rs1569520191 Functional Loss SNV dbSNP153 33..33 33 - - - 98693 RMVar_ID_98693 Human_SNP_ID_716368417 m1A Human chrX + 49001745 49001745 49001745 CGGGCACAGTGGTATCTCCCCCAAAACTTACCACCTCCCACCCGCTAATGGTTCTGCCCTCTCAA CGGGCACAGTGGTATCTCCCCCAAAACTTACCGCCTCCCACCCGCTAATGGTTCTGCCCTCTCAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49001741..49001888 26863196 MeRIP-seq:(Medium) rs1268734601 Functional Loss SNV dbSNP153 33..33 33 - - - 98694 RMVar_ID_98694 Human_SNP_ID_716368493 m1A Human chrX - 49002198 49002198 49002198 CATGGCGCAAGCTCTGTCTGAGGAGGAGTTTCAGCGGATGCAGGTGCCGCTCGCGGTGGGAAAGA CATGGCGCAAGCTCTGTCTGAGGAGGAGTTTCGGCGGATGCAGGTGCCGCTCGCGGTGGGAAAGA T C GRIPAP1 Ensembl:ENSG00000068400 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:49001540..49002250 26863196 MeRIP-seq:(Medium) rs1557068763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848120,Human_RBP_ID_5076132,Human_RBP_ID_5637703,Human_RBP_ID_9443171,Human_RBP_ID_19026654,Human_RBP_ID_21876209 Human_Splice_Rec_2204919,Human_Splice_Rec_2204966,Human_Splice_Rec_2205011,Human_Splice_Rec_2205104,Human_Splice_Rec_2205161,Human_Splice_Rec_2205171,Human_Splice_Rec_2205183 98695 RMVar_ID_98695 Human_SNP_ID_716374710 m1A Human chrX + 49031865 49031865 49031865 GCTCCTAGAATATGGAAAACCACTCCCATCTCAGGGCATCAATCCCAGCCGTGCCCTCTGCCTTG GCTCCTAGAATATGGAAAACCACTCCCATCTCGGGGCATCAATCCCAGCCGTGCCCTCTGCCTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49031864..49032103 26863196 MeRIP-seq:(Medium) rs1417423615 Functional Loss SNV dbSNP153 33..33 33 - - - 98696 RMVar_ID_98696 Human_SNP_ID_716376189 m1A Human chrX + 49039217 49039206 49039218 GATGGCAGGAGAGGCAGGTGCAGGACTGGGGAAGGGAGCCGCGGCGGCCTGTTCCCGACGCTCAC GATGGCAGGAGAGGCAGGTGCA____________GGAGCCGCGGCGGCCTGTTCCCGACGCTCAC AGGACTGGGGAAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49039167..49039340 26863196 MeRIP-seq:(Medium) rs782223948 Functional Loss DEL dbSNP153 23..34 33 - - - 98697 RMVar_ID_98697 Human_SNP_ID_716376977 m1A Human chrX + 49043292 49043292 49043292 GTCGGGCCTCGGCCCGGTCCCCCTAACAAAATAAGAGTCCCCCCTCCCCCCAGCTCGCCACCGCC GTCGGGCCTCGGCCCGGTCCCCCTAACAAAATGAGAGTCCCCCCTCCCCCCAGCTCGCCACCGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49043066..49043472 26863196 MeRIP-seq:(Medium) rs1557076059 Functional Loss SNV dbSNP153 33..33 33 - - - 98698 RMVar_ID_98698 Human_SNP_ID_716376978 m1A Human chrX - 49043297 49043296 49043297 GAGGCGGCGGTGGCGAGCTGGGGGGAGGGGGGACTCTTATTTTGTTAGGGGGACCGGGCCGAGGC GAGGCGGCGGTGGCGAGCTGGGGGGAGGGGGG_CTCTTATTTTGTTAGGGGGACCGGGCCGAGGC GT G TFE3 Ensembl:ENSG00000068323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49043065..49043427 26863196 MeRIP-seq:(Medium) rs1557076061 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_848329,Human_RBP_ID_1062765,Human_RBP_ID_5517789,Human_RBP_ID_8007200,Human_RBP_ID_9339957,Human_RBP_ID_18427849,Human_RBP_ID_27552301 98699 RMVar_ID_98699 Human_SNP_ID_716381604 m1A Human chrX - 49067278 49067278 49067278 AGGGCCTCAGAACTGTTGCTGCGGCGGGTGCGAGCTACGAAGAGGGAGGCGCGATCGGAGGCAGG AGGGCCTCAGAACTGTTGCTGCGGCGGGTGCGGGCTACGAAGAGGGAGGCGCGATCGGAGGCAGG T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:49067258..49067419 26863196 MeRIP-seq:(Medium) rs782231231 Functional Loss SNV dbSNP153 33..33 33 - - - 98700 RMVar_ID_98700 Human_SNP_ID_716382660 m1A Human chrX - 49071727 49071727 49071727 CCCAAACAAAACAGGACATCTGTGACCGCCCTACCCCCACGCCAGCCCCAAACTAAGATATCCCT CCCAAACAAAACAGGACATCTGTGACCGCCCTCCCCCCACGCCAGCCCCAAACTAAGATATCCCT T G AC231657.3,PRAF2 Ensembl:ENSG00000288053,Ensembl:ENSG00000243279 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HeLa cell line,mRNA;HEK293T,Wild Type chrX:49071487..49071825;chrX:49071628..49071800 26863196,26863410 MeRIP-seq:(Medium) rs1311484380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735915 Human_miRNA_ID_194504,Human_miRNA_ID_194505 98701 RMVar_ID_98701 Human_SNP_ID_716382958 m1A Human chrX - 49072828 49072828 49072828 AGTGGAATTGACAAGGAGGAAAGGAGGGGTCTACAAGGGTGAGTCGGGAGCCCTGGCAGATGGGC AGTGGAATTGACAAGGAGGAAAGGAGGGGTCTGCAAGGGTGAGTCGGGAGCCCTGGCAGATGGGC T C AC231657.3,PRAF2 Ensembl:ENSG00000288053,Ensembl:ENSG00000243279 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49072826..49072897 26863196 MeRIP-seq:(Medium) rs967048684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269012,Human_RBP_ID_3930976,Human_RBP_ID_10476449 98702 RMVar_ID_98702 Human_SNP_ID_716383563 m1A Human chrX - 49075606 49075606 49075606 CCCAGAAGGGTACCCTTATTCGCCTCTTTGACACACAATCCAAGGAGAAACTGGTGGAGCTGCGC CCCAGAAGGGTACCCTTATTCGCCTCTTTGACGCACAATCCAAGGAGAAACTGGTGGAGCTGCGC T C AC231657.3,WDR45 Ensembl:ENSG00000288053,Ensembl:ENSG00000196998 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49075543..49075622 26863196 MeRIP-seq:(Medium) rs1557084043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18151797 Human_Splice_Rec_2205375,Human_Splice_Rec_2205391,Human_Splice_Rec_2205399,Human_Splice_Rec_2205417,Human_Splice_Rec_2205435,Human_Splice_Rec_2205451,Human_Splice_Rec_2205470,Human_Splice_Rec_2205490,Human_Splice_Rec_2205509,Human_Splice_Rec_2205531,Human_Splice_Rec_2205549,Human_Splice_Rec_2205557,Human_Splice_Rec_2205565,Human_Splice_Rec_2205566,Human_Splice_Rec_2205586,Human_Splice_Rec_2205602,Human_Splice_Rec_2205620,Human_Splice_Rec_2205632,Human_Splice_Rec_2205645,Human_Splice_Rec_2205660,Human_Splice_Rec_2205664,Human_Splice_Rec_2205678,Human_Splice_Rec_2205689 RMVar_hsa_circ_44266 98703 RMVar_ID_98703 Human_SNP_ID_716383573 m1A Human chrX - 49075652 49075652 49075652 GCCTGTGTGTCTCTAAACCAGCCAGGCACTGTAGTGGCCTCAGCCTCCCAGAAGGGTACCCTTAT GCCTGTGTGTCTCTAAACCAGCCAGGCACTGTGGTGGCCTCAGCCTCCCAGAAGGGTACCCTTAT T C AC231657.3,WDR45 Ensembl:ENSG00000288053,Ensembl:ENSG00000196998 Protein coding,Protein coding CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49075601..49075775 26863196 MeRIP-seq:(Medium) rs782757176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799944,Human_RBP_ID_5066329 Human_Splice_Rec_2205565 Human_miRNA_ID_2054328,Human_miRNA_ID_2716877,Human_miRNA_ID_3052859 RMVar_hsa_circ_44266 98704 RMVar_ID_98704 Human_SNP_ID_716384098 m1A Human chrX + 49078094 49078084 49078094 GGCTGGTCACTCCTCGAAGTGGCTGTTGAGTCATGGTGCAGGATTGTTCCTCTGCATACAAATGG GGCTGGTCACTCCTCGAAGTGGC__________TGGTGCAGGATTGTTCCTCTGCATACAAATGG CTGTTGAGTCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49077996..49078152 26863196 MeRIP-seq:(Medium) rs1557084564 Functional Loss DEL dbSNP153 24..33 33 - - - 98705 RMVar_ID_98705 Human_SNP_ID_716384102 m1A Human chrX + 49078094 49078094 49078094 GGCTGGTCACTCCTCGAAGTGGCTGTTGAGTCATGGTGCAGGATTGTTCCTCTGCATACAAATGG GGCTGGTCACTCCTCGAAGTGGCTGTTGAGTCTTGGTGCAGGATTGTTCCTCTGCATACAAATGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49077996..49078152 26863196 MeRIP-seq:(Medium) rs1569523565 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_606 98706 RMVar_ID_98706 Human_SNP_ID_716384373 m1A Human chrX - 49079689 49079689 49079689 CTTTCGAGTAGGGGTCTAAGGCAGAGGTCTTGAGTGGGTGCTGGCGTTGGAAGGAGCATGCGGCT CTTTCGAGTAGGGGTCTAAGGCAGAGGTCTTGGGTGGGTGCTGGCGTTGGAAGGAGCATGCGGCT T C AC231657.3,WDR45 Ensembl:ENSG00000288053,Ensembl:ENSG00000196998 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:49079686..49079830 32194978 MeRIP-seq:(Medium) rs782434224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2205835 98707 RMVar_ID_98707 Human_SNP_ID_716391448 m1A Human chrX + 49117039 49117039 49117039 AGCTCTACAAGAGGCTCACTCACTGAGATCCAAGGTGTTCTTGTCAAACTCCTGCTGGGAGACAG AGCTCTACAAGAGGCTCACTCACTGAGATCCATGGTGTTCTTGTCAAACTCCTGCTGGGAGACAG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:49115926..49123675 32194978 MeRIP-seq:(Medium) rs1557090360 Functional Loss SNV dbSNP153 33..33 33 - - - 98708 RMVar_ID_98708 Human_SNP_ID_716400292 m1A Human chrX + 49163945 49163945 49163945 CCTGCGCCGGAAGGAGGGTGAGTGACTGGCGCAGGGCCTCCGCTGGGGGAGGGTTCGGAGAGGAG CCTGCGCCGGAAGGAGGGTGAGTGACTGGCGCCGGGCCTCCGCTGGGGGAGGGTTCGGAGAGGAG A C MAGIX Ensembl:ENSG00000269313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:49163944..49164220 26863196 MeRIP-seq:(Medium) rs1178372387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2205925 98709 RMVar_ID_98709 Human_SNP_ID_716400293 m1A Human chrX + 49163945 49163945 49163945 CCTGCGCCGGAAGGAGGGTGAGTGACTGGCGCAGGGCCTCCGCTGGGGGAGGGTTCGGAGAGGAG CCTGCGCCGGAAGGAGGGTGAGTGACTGGCGCGGGGCCTCCGCTGGGGGAGGGTTCGGAGAGGAG A G MAGIX Ensembl:ENSG00000269313 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:49163944..49164220 26863196 MeRIP-seq:(Medium) rs1178372387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2205925 98710 RMVar_ID_98710 Human_SNP_ID_716400353 m1A Human chrX - 49164176 49164176 49164176 CAGGCCCTGCCTCCTCAAAAAGGACCGCCGCCAGAACGGGGGTCCAGTTCCGCACTCTCATCTAA CAGGCCCTGCCTCCTCAAAAAGGACCGCCGCCGGAACGGGGGTCCAGTTCCGCACTCTCATCTAA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49163988..49164216 26863196 MeRIP-seq:(Medium) rs1418347116 Functional Loss SNV dbSNP153 33..33 33 - - - 98711 RMVar_ID_98711 Human_SNP_ID_716400690 m1A Human chrX - 49165385 49165385 49165385 GTGAACCTCTCCCTTCTCCTCACTGATCTCTGACTTCTCTCCCTTGGGAAACCCACCAACTCCTT GTGAACCTCTCCCTTCTCCTCACTGATCTCTGGCTTCTCTCCCTTGGGAAACCCACCAACTCCTT T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49165369..49165434 26863196 MeRIP-seq:(Medium) rs147071787 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98712 RMVar_ID_98712 Human_SNP_ID_716401151 m1A Human chrX + 49167578 49167578 49167578 AATGCGAGAGTCCAGGTGGCCTTGGAGAGGAAAGAGGAACGGTGAAGACAAGCTGCGAGAGCTGG AATGCGAGAGTCCAGGTGGCCTTGGAGAGGAAGGAGGAACGGTGAAGACAAGCTGCGAGAGCTGG A G MAGIX Ensembl:ENSG00000269313 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49167479..49167683 26863196 MeRIP-seq:(Medium) rs985210021 Functional Loss SNV dbSNP153 33..33 33 - - - 98713 RMVar_ID_98713 Human_SNP_ID_716402224 m1A Human chrX + 49173082 49173082 49173082 GTATGGGACCCCCAATTTAAACCAATCTTCTCAGCCCTGGTTGCTGATTGAGGTCCCCTTTCCCA GTATGGGACCCCCAATTTAAACCAATCTTCTCGGCCCTGGTTGCTGATTGAGGTCCCCTTTCCCA A G PLP2 Ensembl:ENSG00000102007 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49173080..49173219 26863196 MeRIP-seq:(Medium) rs369300670 Functional Loss SNV dbSNP153 33..33 33 - - - 98714 RMVar_ID_98714 Human_SNP_ID_716402489 m1A Human chrX + 49174422 49174422 49174422 CCGTTCGGCAGCCAAGACATACAGCAGCCCCCACTGGTAAGTGTGTGTGTGTGTTGGTTGGGGGT CCGTTCGGCAGCCAAGACATACAGCAGCCCCCGCTGGTAAGTGTGTGTGTGTGTTGGTTGGGGGT A G PLP2 Ensembl:ENSG00000102007 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:49174326..49174950 32194978 MeRIP-seq:(Medium) rs1368648435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18197302 Human_Splice_Rec_2205942,Human_Splice_Rec_2205943 RMVar_hsa_circ_7217,RMVar_hsa_circ_88679,RMVar_hsa_circ_262422,RMVar_hsa_circ_262423,RMVar_hsa_circ_104018 98715 RMVar_ID_98715 Human_SNP_ID_716402558 m1A Human chrX + 49174693 49174693 49174693 CTCACCTGCAGACCCCGCAGATGGCCCGGTGTAGGCGAACTTCCCTCATTTCTCTCTGCAATCTG CTCACCTGCAGACCCCGCAGATGGCCCGGTGTGGGCGAACTTCCCTCATTTCTCTCTGCAATCTG A G PLP2 Ensembl:ENSG00000102007 Protein coding stop codon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chrX:49174326..49174914;chrX:49174326..49174747 26863196 MeRIP-seq:(Medium) rs141801067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93465,Human_RBP_ID_8007346,Human_RBP_ID_8719902,Human_RBP_ID_17326504,Human_RBP_ID_17554730,Human_RBP_ID_18197571,Human_RBP_ID_21765592,Human_RBP_ID_26572014,Human_RBP_ID_27163462,Human_RBP_ID_27552335 Human_Splice_Rec_2205944 98716 RMVar_ID_98716 Human_SNP_ID_716402571 m1A Human chrX - 49174751 49174751 49174751 CTGCTGGGAATGTTGTTGTTGGGGTGGGGAGGAGTTATTTCAATGGAGGAGTTATTTGCAGATTG CTGCTGGGAATGTTGTTGTTGGGGTGGGGAGGCGTTATTTCAATGGAGGAGTTATTTGCAGATTG T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49174641..49174851 26863196 MeRIP-seq:(Medium) rs1460939108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3258456 RMVar_hsa_circ_262424 98717 RMVar_ID_98717 Human_SNP_ID_716402573 m1A Human chrX - 49174754 49174754 49174754 GGTCTGCTGGGAATGTTGTTGTTGGGGTGGGGAGGAGTTATTTCAATGGAGGAGTTATTTGCAGA GGTCTGCTGGGAATGTTGTTGTTGGGGTGGGGGGGAGTTATTTCAATGGAGGAGTTATTTGCAGA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:49174326..49174892 26863196 MeRIP-seq:(Medium) rs112741092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3258456 RMVar_hsa_circ_262424 98718 RMVar_ID_98718 Human_SNP_ID_716402588 m1A Human chrX - 49174823 49174823 49174823 TGATTGGCAGGCTGGAAGACAAAAGTCTCCCAATAAAGGCACTTTTACCTCAAAGAGGGGGTGGG TGATTGGCAGGCTGGAAGACAAAAGTCTCCCAGTAAAGGCACTTTTACCTCAAAGAGGGGGTGGG T C PRICKLE3 Ensembl:ENSG00000012211 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:49174775..49174904 26863196 MeRIP-seq:(Medium) rs1356890620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735950 RMVar_hsa_circ_262424 98719 RMVar_ID_98719 Human_SNP_ID_716402612 m1A Human chrX + 49174949 49174949 49174949 GGAGACACCAGTTCTGACTGAACCATGCCCCCACCTAAGTCACAAAATGAGGGAAGTGGGGAGTT GGAGACACCAGTTCTGACTGAACCATGCCCCCGCCTAAGTCACAAAATGAGGGAAGTGGGGAGTT A G PLP2 Ensembl:ENSG00000102007 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:49174926..49174950 26863196 MeRIP-seq:(Medium) rs1223041274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1062771,Human_RBP_ID_17326509,Human_RBP_ID_18151837,Human_RBP_ID_18213431,Human_RBP_ID_21765594,Human_RBP_ID_27552339 Human_miRNA_ID_861852,Human_miRNA_ID_1421996,Human_miRNA_ID_1706492,Human_miRNA_ID_2377095,Human_miRNA_ID_3032741,Human_miRNA_ID_3067603 98720 RMVar_ID_98720 Human_SNP_ID_716402808 m1A Human chrX - 49175983 49175983 49175983 TCCCCCACCCAGGGCCCCCAGCCGTCGCCGCCACCATCATCATAATCACCATCACCATCACAACC TCCCCCACCCAGGGCCCCCAGCCGTCGCCGCCGCCATCATCATAATCACCATCACCATCACAACC T C PRICKLE3 Ensembl:ENSG00000012211 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49175932..49176041 26863196 MeRIP-seq:(Medium) rs1230486950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17441659,Human_RBP_ID_27552344 98721 RMVar_ID_98721 Human_SNP_ID_716403587 m1A Human chrX - 49179390 49179390 49179390 AGGGAGGAGCCTGGGAGATGCCTTCTCCTCCCAGGCACAGTACTGCACAGCACTGGAAGAGGAGG AGGGAGGAGCCTGGGAGATGCCTTCTCCTCCCGGGCACAGTACTGCACAGCACTGGAAGAGGAGG T C PRICKLE3 Ensembl:ENSG00000012211 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49179375..49179713 26863196 MeRIP-seq:(Medium) rs782073511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3977328 98722 RMVar_ID_98722 Human_SNP_ID_716414865 m1A Human chrX + 49235562 49235562 49235562 CCGTGACACTCTGTGGACCGCGAGCACGGAGCAGGGTTTCTACAGCTGCTCCCCACTTTCTCGGA CCGTGACACTCTGTGGACCGCGAGCACGGAGCCGGGTTTCTACAGCTGCTCCCCACTTTCTCGGA A C CCDC22 Ensembl:ENSG00000101997 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:49235513..49235616 26863196 MeRIP-seq:(Medium) rs1557112487 Functional Loss SNV dbSNP153 33..33 33 - - - 98723 RMVar_ID_98723 Human_SNP_ID_716417225 m1A Human chrX - 49247720 49247720 49247720 CCCAGGGTCTTCATGTCGGCCTCAACCTCCTCAATGCTGCGGTTCACTCCTTCCAGCTGCTCCCG CCCAGGGTCTTCATGTCGGCCTCAACCTCCTCGATGCTGCGGTTCACTCCTTCCAGCTGCTCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49247670..49247744 26863196 MeRIP-seq:(Medium) rs782294044 Functional Loss SNV dbSNP153 33..33 33 - - - 98724 RMVar_ID_98724 Human_SNP_ID_716417439 m1A Human chrX - 49248438 49248438 49248438 CCCGGTGCTTCTCCCACTGACCCGCCAAGTGGATGACCCGCTGGGCACTATTCTCCACCACAAGC CCCGGTGCTTCTCCCACTGACCCGCCAAGTGGGTGACCCGCTGGGCACTATTCTCCACCACAAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:49248426..49248475 32194978 MeRIP-seq:(Medium) rs782575845 Functional Loss SNV dbSNP153 33..33 33 - - - 98725 RMVar_ID_98725 Human_SNP_ID_716418207 m1A Human chrX - 49252028 49252028 49252028 CTTTCACCTCACTTCAGCCCTAGCCCTGAACAAGACCCCACTCCCAACCTCAGTCCTGATCCCTT CTTTCACCTCACTTCAGCCCTAGCCCTGAACACGACCCCACTCCCAACCTCAGTCCTGATCCCTT T G FOXP3 Ensembl:ENSG00000049768 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:49251977..49252117 26863196 MeRIP-seq:(Medium) rs367551684 Functional Loss SNV dbSNP153 33..33 33 - - - 98726 RMVar_ID_98726 Human_SNP_ID_716424059 m1A Human chrX - 49282665 49282665 49282665 TGCTGCGCTGGCTTCTACACTGTCCCTCACACACGTTAGTCATGGCCTCACCTCAGGAACTTCAC TGCTGCGCTGGCTTCTACACTGTCCCTCACACGCGTTAGTCATGGCCTCACCTCAGGAACTTCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49282357..49282983 26863196 MeRIP-seq:(Medium) rs781867138 Functional Loss SNV dbSNP153 33..33 33 - - - 98727 RMVar_ID_98727 Human_SNP_ID_716424861 m1A Human chrX + 49286570 49286570 49286570 GTGGCTCCCATGGGCAGAGGGCTCAGGATGTGACGGCCCTGTGGTTCTGGGTACAGAGGGTCAGT GTGGCTCCCATGGGCAGAGGGCTCAGGATGTGGCGGCCCTGTGGTTCTGGGTACAGAGGGTCAGT A G PPP1R3F Ensembl:ENSG00000049769 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49286519..49286733 26863196 MeRIP-seq:(Medium) rs368025864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_282312 98728 RMVar_ID_98728 Human_SNP_ID_716436993 m1A Human chrX + 49591294 49591294 49591294 TCAGGATCCTGCAGCTGCTCAGGAGGGACAGGATGAGGGAGCATCTGCAGGTCAAGGTGAGGGAA TCAGGATCCTGCAGCTGCTCAGGAGGGACAGGGTGAGGGAGCATCTGCAGGTCAAGGTGAGGGAA A G GAGE1,GAGE2A Ensembl:ENSG00000205777,Ensembl:ENSG00000189064 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49591243..49591351 26863196 MeRIP-seq:(Medium) rs1557130473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2206727,Human_Splice_Rec_2206728 98729 RMVar_ID_98729 Human_SNP_ID_716456593 m1A Human chrX - 49691297 49691297 49691297 CTGGGTGTGAGCTTGGAGATGGTCCTGATACCAAGAGGGTGTGCCTGCGAAATGAAGAGCAGATG CTGGGTGTGAGCTTGGAGATGGTCCTGATACCGAGAGGGTGTGCCTGCGAAATGAAGAGCAGATG T C PAGE1 Ensembl:ENSG00000068985 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49691202..49691326 26863196 MeRIP-seq:(Medium) rs868930525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2206737 RMVar_hsa_circ_74256 98730 RMVar_ID_98730 Human_SNP_ID_716489187 m1A Human chrX + 49879642 49879606 49879642 CGGGGAAGGTGGACGCCACCGAGAAGGTGGAGACGGCGGGGAAGGTGGACGCCGCTGGGAAGGTG _________________________________CGGCGGGGAAGGTGGACGCCGCTGGGAAGGTG GCGGCGGGGAAGGTGGACGCCACCGAGAAGGTGGAGA G USP27X Ensembl:ENSG00000273820 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chrX:49879475..49879902;chrX:49879598..49879727 26863196 MeRIP-seq:(Medium) rs1475528682 Functional Loss DEL dbSNP153 1..33 33 - - - 98731 RMVar_ID_98731 Human_SNP_ID_716489196 m1A Human chrX + 49879627 49879627 49879627 GGAAGGCGGAGGCGGCGGGGAAGGTGGACGCCACCGAGAAGGTGGAGACGGCGGGGAAGGTGGAC GGAAGGCGGAGGCGGCGGGGAAGGTGGACGCCCCCGAGAAGGTGGAGACGGCGGGGAAGGTGGAC A C USP27X Ensembl:ENSG00000273820 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49879577..49879895 26863196 MeRIP-seq:(Medium) rs1318837778 Functional Loss SNV dbSNP153 33..33 33 - - - 98732 RMVar_ID_98732 Human_SNP_ID_716489197 m1A Human chrX + 49879627 49879627 49879627 GGAAGGCGGAGGCGGCGGGGAAGGTGGACGCCACCGAGAAGGTGGAGACGGCGGGGAAGGTGGAC GGAAGGCGGAGGCGGCGGGGAAGGTGGACGCCGCCGAGAAGGTGGAGACGGCGGGGAAGGTGGAC A G USP27X Ensembl:ENSG00000273820 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49879577..49879895 26863196 MeRIP-seq:(Medium) rs1318837778 Functional Loss SNV dbSNP153 33..33 33 - - - 98733 RMVar_ID_98733 Human_SNP_ID_716489203 m1A Human chrX + 49879642 49879642 49879642 CGGGGAAGGTGGACGCCACCGAGAAGGTGGAGACGGCGGGGAAGGTGGACGCCGCTGGGAAGGTG CGGGGAAGGTGGACGCCACCGAGAAGGTGGAGGCGGCGGGGAAGGTGGACGCCGCTGGGAAGGTG A G USP27X Ensembl:ENSG00000273820 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chrX:49879475..49879902;chrX:49879598..49879727 26863196 MeRIP-seq:(Medium) rs1330304327 Functional Loss SNV dbSNP153 33..33 33 - - - 98734 RMVar_ID_98734 Human_SNP_ID_716635589 m1A Human chrX - 50813160 50813139 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC_____________________GCCAGGGTTTGT CGGCGGCGGCGGCGGCGGCAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1348843321 Functional Loss DEL dbSNP153 33..53 33 - - - 98735 RMVar_ID_98735 Human_SNP_ID_716635591 m1A Human chrX - 50813160 50813142 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC__________________GCCGCCAGGGTTTGT CGGCGGCGGCGGCGGCAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1301555508 Functional Loss DEL dbSNP153 33..50 33 - - - 98736 RMVar_ID_98736 Human_SNP_ID_716635594 m1A Human chrX - 50813160 50813145 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC_______________GCCGCCGCCAGGGTTTGT CGGCGGCGGCGGCAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs782571334 Functional Loss DEL dbSNP153 33..47 33 - - - 98737 RMVar_ID_98737 Human_SNP_ID_716635599 m1A Human chrX - 50813160 50813148 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC____________GCCGCCGCCGCCAGGGTTTGT CGGCGGCGGCAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1181019696 Functional Loss DEL dbSNP153 33..44 33 - - - 98738 RMVar_ID_98738 Human_SNP_ID_716635604 m1A Human chrX - 50813160 50813154 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC______GCCGCCGCCGCCGCCGCCAGGGTTTGT CGGCAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1569549444 Functional Loss DEL dbSNP153 33..38 33 - - - 98739 RMVar_ID_98739 Human_SNP_ID_716635610 m1A Human chrX - 50813160 50813157 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCC___GCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CAGT C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1287903137 Functional Loss DEL dbSNP153 33..35 33 - - - 98740 RMVar_ID_98740 Human_SNP_ID_716635613 m1A Human chrX - 50813160 50813158 50813161 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGC___TGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT AGTG A SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs1310629036 Functional Loss DEL dbSNP153 32..34 33 - - - 98741 RMVar_ID_98741 Human_SNP_ID_716635617 m1A Human chrX - 50813160 50813160 50813160 CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT CCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCGCTGCCGCCGCCGCCGCCGCCGCCAGGGTTTGT T C SHROOM4 Ensembl:ENSG00000158352 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:50813118..50813192 26863196 MeRIP-seq:(Medium) rs372441873 Functional Loss SNV dbSNP153 33..33 33 - - - 98742 RMVar_ID_98742 Human_SNP_ID_716727114 m1A Human chrX + 51332989 51332989 51332989 GCCTCGAGGATGAAGTGCAAACCCAACCAGACACGGACCTACGACCCCGAGGGGTTCAAGAAGCG GCCTCGAGGATGAAGTGCAAACCCAACCAGACGCGGACCTACGACCCCGAGGGGTTCAAGAAGCG A G NUDT10 Ensembl:ENSG00000122824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs2625875 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98743 RMVar_ID_98743 Human_SNP_ID_716821844 m1A Human chrX + 51895384 51895384 51895384 AAATGCTACCCCAAAGGGTCCAAATGCTGCCTATGATTTTTCCCAGGCAGCAACCACTGGTGAGT AAATGCTACCCCAAAGGGTCCAAATGCTGCCTGTGATTTTTCCCAGGCAGCAACCACTGGTGAGT A G MAGED1 Ensembl:ENSG00000179222 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:51895334..51895583 32194978 MeRIP-seq:(Medium) rs782765353 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18151978,Human_RBP_ID_22123392,Human_RBP_ID_22841616,Human_RBP_ID_26834770,Human_RBP_ID_27382808 RMVar_hsa_circ_54425,RMVar_hsa_circ_100426,RMVar_hsa_circ_115453,RMVar_hsa_circ_262445,RMVar_hsa_circ_93696,RMVar_hsa_circ_262448,RMVar_hsa_circ_125237,RMVar_hsa_circ_262446,RMVar_hsa_circ_262447,RMVar_hsa_circ_275038,RMVar_hsa_circ_315936,RMVar_hsa_circ_262449 98744 RMVar_ID_98744 Human_SNP_ID_716822132 m1A Human chrX + 51896851 51896834 51896852 CCCACCGGGCTGGCAGGGTCCTCCAGACTGGCAAGGTCCTCCTGACTGGCCGCTACCACCCGACT CCCACCGGGCTGGCAG__________________GGTCCTCCTGACTGGCCGCTACCACCCGACT GGGTCCTCCAGACTGGCAA G MAGED1 Ensembl:ENSG00000179222 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1557364345 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_736149,Human_RBP_ID_22467955,Human_RBP_ID_22778154 Human_miRNA_ID_2402781 RMVar_hsa_circ_100426,RMVar_hsa_circ_115453,RMVar_hsa_circ_262445,RMVar_hsa_circ_93696,RMVar_hsa_circ_262448,RMVar_hsa_circ_125237,RMVar_hsa_circ_262446,RMVar_hsa_circ_262447,RMVar_hsa_circ_275038,RMVar_hsa_circ_262449,RMVar_hsa_circ_82947,RMVar_hsa_circ_262451 98745 RMVar_ID_98745 Human_SNP_ID_716822135 m1A Human chrX + 51896851 51896851 51896851 CCCACCGGGCTGGCAGGGTCCTCCAGACTGGCAAGGTCCTCCTGACTGGCCGCTACCACCCGACT CCCACCGGGCTGGCAGGGTCCTCCAGACTGGCGAGGTCCTCCTGACTGGCCGCTACCACCCGACT A G MAGED1 Ensembl:ENSG00000179222 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1557364351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736149,Human_RBP_ID_22467955,Human_RBP_ID_22778154 Human_miRNA_ID_2402781 RMVar_hsa_circ_100426,RMVar_hsa_circ_115453,RMVar_hsa_circ_262445,RMVar_hsa_circ_93696,RMVar_hsa_circ_262448,RMVar_hsa_circ_125237,RMVar_hsa_circ_262446,RMVar_hsa_circ_262447,RMVar_hsa_circ_275038,RMVar_hsa_circ_262449,RMVar_hsa_circ_82947,RMVar_hsa_circ_262451 98746 RMVar_ID_98746 Human_SNP_ID_716822180 m1A Human chrX + 51897026 51897026 51897026 AACCTGCGCCCTTCTCCCAACTCGCGTGCCTCACAGAACCCAGGTGCTGCACAGCCCCGAGATGT AACCTGCGCCCTTCTCCCAACTCGCGTGCCTCGCAGAACCCAGGTGCTGCACAGCCCCGAGATGT A G MAGED1 Ensembl:ENSG00000179222 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:51896976..51897100 32194978 MeRIP-seq:(Medium) rs781885812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257563 Human_Splice_Rec_2207365,Human_Splice_Rec_2207387,Human_Splice_Rec_2207411,Human_Splice_Rec_2207437,Human_Splice_Rec_2207471 Human_miRNA_ID_2673675 RMVar_hsa_circ_100426,RMVar_hsa_circ_115453,RMVar_hsa_circ_262445,RMVar_hsa_circ_93696,RMVar_hsa_circ_262448,RMVar_hsa_circ_125237,RMVar_hsa_circ_262446,RMVar_hsa_circ_262447,RMVar_hsa_circ_275038,RMVar_hsa_circ_262449,RMVar_hsa_circ_82947,RMVar_hsa_circ_262451 98747 RMVar_ID_98747 Human_SNP_ID_717001655 m1A Human chrX + 53082408 53082408 53082408 TGGTGAGGAGAGCTGGTTGCGTGAGTCTCCTCAGCTCTGCTTACCGGTGCGACTAGCGGCAGCGA TGGTGAGGAGAGCTGGTTGCGTGAGTCTCCTCGGCTCTGCTTACCGGTGCGACTAGCGGCAGCGA A G TSPYL2 Ensembl:ENSG00000184205 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:53082351..53082685;chrX:53082351..53083245 26863196 MeRIP-seq:(Medium) rs1205772059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_799841,Human_RBP_ID_1715877,Human_RBP_ID_5066815,Human_RBP_ID_5277843,Human_RBP_ID_8720005,Human_RBP_ID_18427851,Human_RBP_ID_22348259 RMVar_hsa_circ_82347,RMVar_hsa_circ_262467 98748 RMVar_ID_98748 Human_SNP_ID_717001710 m1A Human chrX + 53082554 53082554 53082554 TCCGGCCAAGACCCGCCGCCTGAGCAGCTCCGAGTCTCCACAGCGCGACCCGCCCCCGCCGCCGC TCCGGCCAAGACCCGCCGCCTGAGCAGCTCCGGGTCTCCACAGCGCGACCCGCCCCCGCCGCCGC A G TSPYL2 Ensembl:ENSG00000184205 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:53082459..53082613 26863410 MeRIP-seq:(Medium) rs1556807146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82347,RMVar_hsa_circ_262467 98749 RMVar_ID_98749 Human_SNP_ID_717002033 m1A Human chrX + 53083424 53083424 53083424 GGAGGAGAGCCAGAGGTGGGCATGATCCCCCTATCGGAAGACGGACTAGACTGGGTGGAAGAGGG GGAGGAGAGCCAGAGGTGGGCATGATCCCCCTGTCGGAAGACGGACTAGACTGGGTGGAAGAGGG A G TSPYL2 Ensembl:ENSG00000184205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53083381..53083739 26863196 MeRIP-seq:(Medium) rs1182939709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82347,RMVar_hsa_circ_262467 98750 RMVar_ID_98750 Human_SNP_ID_717002704 m1A Human chrX + 53085666 53085666 53085666 AACCAGGGGCAGATGTGAGGTGGTGATCATGGAAGACGCCCCTGACTATTATGCAGTGGAAGACA AACCAGGGGCAGATGTGAGGTGGTGATCATGGGAGACGCCCCTGACTATTATGCAGTGGAAGACA A G TSPYL2 Ensembl:ENSG00000184205 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53085641..53085792 26863196 MeRIP-seq:(Medium) rs1556808325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18921149,Human_RBP_ID_26362847 Human_Splice_Rec_2208297,Human_Splice_Rec_2208303,Human_Splice_Rec_2208311,Human_Splice_Rec_2208319 RMVar_hsa_circ_89273,RMVar_hsa_circ_82347,RMVar_hsa_circ_262467,RMVar_hsa_circ_262469 98751 RMVar_ID_98751 Human_SNP_ID_717002782 m1A Human chrX + 53085873 53085873 53085873 CCACAATGAGGTCCCCAACAACGAGACCACTGATAACAACGAGAGTGCTGATGACCACGAAACCA CCACAATGAGGTCCCCAACAACGAGACCACTGGTAACAACGAGAGTGCTGATGACCACGAAACCA A G TSPYL2 Ensembl:ENSG00000184205 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53085822..53086322 26863196 MeRIP-seq:(Medium) rs782642668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5066857,Human_RBP_ID_17554757 RMVar_hsa_circ_89273,RMVar_hsa_circ_82347,RMVar_hsa_circ_262467,RMVar_hsa_circ_262469 98752 RMVar_ID_98752 Human_SNP_ID_717002889 m1A Human chrX + 53086149 53086149 53086149 TGGCAACGAAGGTGACAATGAGGGCAGTGATGATGATGGCAATGAAGGTGACAATGAAGGCAGCG TGGCAACGAAGGTGACAATGAGGGCAGTGATGGTGATGGCAATGAAGGTGACAATGAAGGCAGCG A G TSPYL2 Ensembl:ENSG00000184205 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53085816..53086341 26863196 MeRIP-seq:(Medium) rs1313435123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967336,Human_RBP_ID_16902471,Human_RBP_ID_26362849 RMVar_hsa_circ_89273,RMVar_hsa_circ_82347,RMVar_hsa_circ_262467,RMVar_hsa_circ_262469 98753 RMVar_ID_98753 Human_SNP_ID_717003395 m1A Human chrX - 53087739 53087739 53087739 ATAGGGGAGAAGCAAGGAAGGGGAAATGGAGGAAGGCAGTTAGATGAGCAGATAGGTGTCACTCT ATAGGGGAGAAGCAAGGAAGGGGAAATGGAGGCAGGCAGTTAGATGAGCAGATAGGTGTCACTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53087736..53087896 26863196 MeRIP-seq:(Medium) rs1350989223 Functional Loss SNV dbSNP153 33..33 33 - - - 98754 RMVar_ID_98754 Human_SNP_ID_717003601 m1A Human chrX - 53088361 53088361 53088361 AAGAGGAGAGGGATGGAGAAAGAACTTGGGAGAGGAAGGTGGCAGCAGCGCCTCCATGGGCACTG AAGAGGAGAGGGATGGAGAAAGAACTTGGGAGTGGAAGGTGGCAGCAGCGCCTCCATGGGCACTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53088312..53088490 26863196 MeRIP-seq:(Medium) rs1343300598 Functional Loss SNV dbSNP153 33..33 33 - - - 98755 RMVar_ID_98755 Human_SNP_ID_717021507 m1A Human chrX + 53192544 53192544 53192544 AGAGGGAGAAGGGGGTAGGAAGGAAGGAAAAGAGGGGAGGAGAGTGGGGGCAGGGGTTAGTGTAG AGAGGGAGAAGGGGGTAGGAAGGAAGGAAAAGGGGGGAGGAGAGTGGGGGCAGGGGTTAGTGTAG A G NONHSAG054550.2-001,RF00017-4630 RNACentral:URS00009C0EF1,RNACentral:URS000096585E lincRNA,SRP RNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53192494..53192649 26863196 MeRIP-seq:(Medium) rs1427338289 Functional Loss SNV dbSNP153 33..33 33 - - - 98756 RMVar_ID_98756 Human_SNP_ID_717021516 m1A Human chrX - 53192579 53192579 53192579 CTTCTCTCCCCAGTTCTGGTCCTGGCCAGGCCATGCTACACTAACCCCTGCCCCCACTCTCCTCC CTTCTCTCCCCAGTTCTGGTCCTGGCCAGGCCTTGCTACACTAACCCCTGCCCCCACTCTCCTCC T A KDM5C Ensembl:ENSG00000126012 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53192532..53192642 26863196 MeRIP-seq:(Medium) rs1205352594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736260,Human_RBP_ID_21876256,Human_RBP_ID_21907738,Human_RBP_ID_24527006 98757 RMVar_ID_98757 Human_SNP_ID_717021641 m1A Human chrX + 53192963 53192963 53192963 GGTCTCTGTCAGGGTCTGTGCTAGGCTCAGCCACTGTCACAACTGTTGCTGAGGCGGCTGCTGTG GGTCTCTGTCAGGGTCTGTGCTAGGCTCAGCCCCTGTCACAACTGTTGCTGAGGCGGCTGCTGTG A C NONHSAG054550.2-002,NONHSAG054550.2-001,RF00017-4630 RNACentral:URS00008BBD06,RNACentral:URS00009C0EF1,RNACentral:URS000096585E lincRNA,lincRNA,SRP RNA intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:53192926..53193071 26863196 MeRIP-seq:(Medium) rs1208494015 Functional Loss SNV dbSNP153 33..33 33 - - - 98758 RMVar_ID_98758 Human_SNP_ID_717021720 m1A Human chrX - 53193241 53193241 53193241 GCGGCGGAAGGTGGATCGGGGTGGGGAGGGCGATGACCCAGCCCGAGAGGAGCTAGAGCCAAAGA GCGGCGGAAGGTGGATCGGGGTGGGGAGGGCGGTGACCCAGCCCGAGAGGAGCTAGAGCCAAAGA T C KDM5C Ensembl:ENSG00000126012 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:53193101..53193492 26863196 MeRIP-seq:(Medium) rs1556832487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94831,Human_RBP_ID_3976539,Human_RBP_ID_5091158,Human_RBP_ID_8008299,Human_RBP_ID_8731569,Human_RBP_ID_8935991,Human_RBP_ID_9317369,Human_RBP_ID_18173855,Human_RBP_ID_19148415,Human_RBP_ID_21997275,Human_RBP_ID_24394122,Human_RBP_ID_26282512,Human_RBP_ID_26797167,Human_RBP_ID_27844018 Human_Splice_Rec_2208432,Human_Splice_Rec_2208478,Human_Splice_Rec_2208527,Human_Splice_Rec_2208574 98759 RMVar_ID_98759 Human_SNP_ID_717022214 m1A Human chrX - 53195312 53195312 53195312 GTGGGGCTGGAGGAGCTGAGACAGCTAGAGCTACAGGTACTGACAGCGCACTCCTGGAGGGAGAA GTGGGGCTGGAGGAGCTGAGACAGCTAGAGCTGCAGGTACTGACAGCGCACTCCTGGAGGGAGAA T C KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:53195262..53195425 26863196 MeRIP-seq:(Medium) rs1556835910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93797,Human_RBP_ID_736276,Human_RBP_ID_1715909,Human_RBP_ID_2075510,Human_RBP_ID_8008324,Human_RBP_ID_8936021,Human_RBP_ID_9265265,Human_RBP_ID_9409867,Human_RBP_ID_18921202,Human_RBP_ID_23102578,Human_RBP_ID_27149140 Human_Splice_Rec_2208376,Human_Splice_Rec_2208377,Human_Splice_Rec_2208423,Human_Splice_Rec_2208424,Human_Splice_Rec_2208468,Human_Splice_Rec_2208469,Human_Splice_Rec_2208517,Human_Splice_Rec_2208518,Human_Splice_Rec_2208565,Human_Splice_Rec_2208566 RMVar_hsa_circ_49092,RMVar_hsa_circ_119424,RMVar_hsa_circ_115048,RMVar_hsa_circ_262471,RMVar_hsa_circ_262472,RMVar_hsa_circ_66579 98760 RMVar_ID_98760 Human_SNP_ID_717022217 m1A Human chrX - 53195324 53195324 53195324 CGGGACCTACCTGTGGGGCTGGAGGAGCTGAGACAGCTAGAGCTACAGGTACTGACAGCGCACTC CGGGACCTACCTGTGGGGCTGGAGGAGCTGAGGCAGCTAGAGCTACAGGTACTGACAGCGCACTC T C KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53195274..53195422 26863196 MeRIP-seq:(Medium) rs1288344996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93797,Human_RBP_ID_257336,Human_RBP_ID_8008325,Human_RBP_ID_8936022,Human_RBP_ID_9265265,Human_RBP_ID_18197574 Human_Splice_Rec_2208376,Human_Splice_Rec_2208377,Human_Splice_Rec_2208423,Human_Splice_Rec_2208424,Human_Splice_Rec_2208468,Human_Splice_Rec_2208469,Human_Splice_Rec_2208517,Human_Splice_Rec_2208518,Human_Splice_Rec_2208565,Human_Splice_Rec_2208566 Human_miRNA_ID_1968956 RMVar_hsa_circ_49092,RMVar_hsa_circ_119424,RMVar_hsa_circ_115048,RMVar_hsa_circ_262471,RMVar_hsa_circ_262472,RMVar_hsa_circ_66579 98761 RMVar_ID_98761 Human_SNP_ID_717022519 m1A Human chrX + 53196893 53196893 53196893 GTTTCACCTCATCCAGCCATCGCGCCTGTTCCACCTGCCGCTGGAGCTGCTGGGCCTCAGGCACC GTTTCACCTCATCCAGCCATCGCGCCTGTTCCCCCTGCCGCTGGAGCTGCTGGGCCTCAGGCACC A C NONHSAG054550.2-001,RF00017-4630 RNACentral:URS00009C0EF1,RNACentral:URS000096585E lincRNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53196763..53196967 26863196 MeRIP-seq:(Medium) rs201172759 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 98762 RMVar_ID_98762 Human_SNP_ID_717025257 m1A Human chrX - 53210462 53210462 53210462 CTATTTGATAGCCAGCCTGACCTCCTGCACCAACTTGTCACCCTCATGAATCCCAACACCCTCAT CTATTTGATAGCCAGCCTGACCTCCTGCACCAGCTTGTCACCCTCATGAATCCCAACACCCTCAT T C KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53210379..53210525 26863196 MeRIP-seq:(Medium) rs782503580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736290,Human_RBP_ID_799456,Human_RBP_ID_2075535,Human_RBP_ID_8008473,Human_RBP_ID_8720092,Human_RBP_ID_8936085,Human_RBP_ID_9265270,Human_RBP_ID_9316812,Human_RBP_ID_17326569,Human_RBP_ID_17554795,Human_RBP_ID_18152101,Human_RBP_ID_27552461 Human_Splice_Rec_2208360,Human_Splice_Rec_2208407,Human_Splice_Rec_2208453,Human_Splice_Rec_2208501,Human_Splice_Rec_2208548,Human_Splice_Rec_2208581,Human_Splice_Rec_2208589 RMVar_hsa_circ_107587,RMVar_hsa_circ_262474,RMVar_hsa_circ_87242,RMVar_hsa_circ_119816,RMVar_hsa_circ_262475,RMVar_hsa_circ_262476 98763 RMVar_ID_98763 Human_SNP_ID_717025298 m1A Human chrX - 53210732 53210732 53210732 GTGCCCTGGCTCTACGTGGGCATGGTCTTCTCAGCCTTTTGCTGGCATATTGAGGATCACTGGAG GTGCCCTGGCTCTACGTGGGCATGGTCTTCTCGGCCTTTTGCTGGCATATTGAGGATCACTGGAG T C KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:53210585..53210757 32194978 MeRIP-seq:(Medium) rs1556848360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736292,Human_RBP_ID_1230919,Human_RBP_ID_1715937,Human_RBP_ID_2075538,Human_RBP_ID_9247619 Human_Splice_Rec_2208358,Human_Splice_Rec_2208405,Human_Splice_Rec_2208451,Human_Splice_Rec_2208499,Human_Splice_Rec_2208546,Human_Splice_Rec_2208579 Human_miRNA_ID_2883760 RMVar_hsa_circ_107587,RMVar_hsa_circ_262474,RMVar_hsa_circ_112417,RMVar_hsa_circ_87242,RMVar_hsa_circ_262476,RMVar_hsa_circ_262477 98764 RMVar_ID_98764 Human_SNP_ID_717026282 m1A Human chrX + 53216103 53216103 53216103 TACCTTTCTTCCGCAGAGTCTTGTCTTTGGCCATGAGGCCCAGGCCCATCATCTTGGGGCCTGCC TACCTTTCTTCCGCAGAGTCTTGTCTTTGGCCTTGAGGCCCAGGCCCATCATCTTGGGGCCTGCC A T NONHSAG054550.2-001 RNACentral:URS00009C0EF1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53215971..53216104 26863196 MeRIP-seq:(Medium) rs1164651373 Functional Loss SNV dbSNP153 33..33 33 - - - 98765 RMVar_ID_98765 Human_SNP_ID_717027856 m1A Human chrX + 53225166 53225166 53225166 CCGCAGCCTTCGCCACCACAGTTACCTCCCAAACGCCGCGGCCTTCAGCGCCGCCGCCGCCATCT CCGCAGCCTTCGCCACCACAGTTACCTCCCAATCGCCGCGGCCTTCAGCGCCGCCGCCGCCATCT A T NONHSAG054550.2-001 RNACentral:URS00009C0EF1 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:53224812..53225225;chrX:53225014..53225225 26863196 MeRIP-seq:(Medium) rs1046550824 Functional Loss SNV dbSNP153 33..33 33 - - - 98766 RMVar_ID_98766 Human_SNP_ID_717029242 m1A Human chrX - 53233773 53233773 53233773 CCCTGGGGCTCCTCTGGCCGTGTGGGGCTAGGAGAGCGCTCTGTAGAGTTGTGGCCAAACTTCAG CCCTGGGGCTCCTCTGGCCGTGTGGGGCTAGGGGAGCGCTCTGTAGAGTTGTGGCCAAACTTCAG T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53233733..53233834 32194978 MeRIP-seq:(Medium) rs1401289442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26573790 98767 RMVar_ID_98767 Human_SNP_ID_717029332 m1A Human chrX - 53234281 53234281 53234281 ATGGCCCGCTGCACGCCTCTGGGCCCCCTGGCACAGCCAACCCCCCCAGTGCAAACCCCAAGGCC ATGGCCCGCTGCACGCCTCTGGGCCCCCTGGCGCAGCCAACCCCCCCAGTGCAAACCCCAAGGCC T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53234232..53234303 26863196 MeRIP-seq:(Medium) rs1556858938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5330471,Human_RBP_ID_17095874,Human_RBP_ID_17580287,Human_RBP_ID_26573793 98768 RMVar_ID_98768 Human_SNP_ID_717029362 m1A Human chrX - 53234360 53234360 53234360 CCACCCCACCCCTCCTATCCACCCCTCCCCCCACCCTCCCCTCACACCCCGCACTCACCCCTTCC CCACCCCACCCCTCCTATCCACCCCTCCCCCCCCCCTCCCCTCACACCCCGCACTCACCCCTTCC T G IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53234333..53234434 32194978 MeRIP-seq:(Medium) rs797044650 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1421921,Human_miRNA_ID_1706394 98769 RMVar_ID_98769 Human_SNP_ID_717034972 m1A Human chrX - 53266896 53266896 53266896 AAGCCTTAACCAGCCCCTCCTTCCCCCCACCCACCCCCCCGCAGATTCCCCCATGGGACCCTGTC AAGCCTTAACCAGCCCCTCCTTCCCCCCACCCCCCCCCCCGCAGATTCCCCCATGGGACCCTGTC T G IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53266847..53267048 32194978 MeRIP-seq:(Medium) rs868920830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262485,RMVar_hsa_circ_127110 98770 RMVar_ID_98770 Human_SNP_ID_717034993 m1A Human chrX - 53266990 53266990 53266990 AGACGCTCACCAGTTCTGCTGTCCGGCCTCCGAGTGCAGTAGTCCCTCCTCTCGGTAACTGAGAG AGACGCTCACCAGTTCTGCTGTCCGGCCTCCGGGTGCAGTAGTCCCTCCTCTCGGTAACTGAGAG T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53266947..53267041 26863196 MeRIP-seq:(Medium) rs781829948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2208784,Human_Splice_Rec_2208785,Human_Splice_Rec_2208794,Human_Splice_Rec_2208796,Human_Splice_Rec_2208800,Human_Splice_Rec_2208804 RMVar_hsa_circ_262485,RMVar_hsa_circ_127110 98771 RMVar_ID_98771 Human_SNP_ID_717035482 m1A Human chrX - 53270345 53270343 53270346 GGAGACCAGTGTGATGGGGAAAAGGCTGAAGAAGGAGTGAGAGGAGTAGAAGATGAGATGGTAGG GGAGACCAGTGTGATGGGGAAAAGGCTGAAG___GAGTGAGAGGAGTAGAAGATGAGATGGTAGG CCTT C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53270336..53270484 26863196 MeRIP-seq:(Medium) rs1221205101 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_24346305 RMVar_hsa_circ_262485,RMVar_hsa_circ_127110 98772 RMVar_ID_98772 Human_SNP_ID_717037590 m1A Human chrX - 53281558 53281558 53281558 GAGGGGGTGGTGACACGGTGGAGACACCGGCTAGGCCAGGGGGCCTGCCCTTGGGACAGGTCCAG GAGGGGGTGGTGACACGGTGGAGACACCGGCTGGGCCAGGGGGCCTGCCCTTGGGACAGGTCCAG T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53281446..53281563 26863196 MeRIP-seq:(Medium) rs1556870892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5067243 Human_Splice_Rec_2208726,Human_Splice_Rec_2208776,Human_Splice_Rec_2208781,Human_Splice_Rec_2208787,Human_Splice_Rec_2208791,Human_Splice_Rec_2208795,Human_Splice_Rec_2208797,Human_Splice_Rec_2208805 RMVar_hsa_circ_262485,RMVar_hsa_circ_127110 98773 RMVar_ID_98773 Human_SNP_ID_717054242 m1A Human chrX - 53383222 53383222 53383222 GGATGCCCAGGCTGAGGAAGAGATCAAGCAAGAGATGAACACACTGCAGCAGAAGCTGAATGAGC GGATGCCCAGGCTGAGGAAGAGATCAAGCAAGGGATGAACACACTGCAGCAGAAGCTGAATGAGC T C SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53383171..53383285 26863196 MeRIP-seq:(Medium) rs781938970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16389,Human_RBP_ID_92921,Human_RBP_ID_968205,Human_RBP_ID_1716102,Human_RBP_ID_2075636,Human_RBP_ID_3924377,Human_RBP_ID_8008821,Human_RBP_ID_8720193,Human_RBP_ID_9317426,Human_RBP_ID_9409210,Human_RBP_ID_16904086,Human_RBP_ID_19148424,Human_RBP_ID_22468361,Human_RBP_ID_26362867,Human_RBP_ID_27833841 Human_Splice_Rec_2208843,Human_Splice_Rec_2208892,Human_Splice_Rec_2208906 RMVar_hsa_circ_71480 98774 RMVar_ID_98774 Human_SNP_ID_717056442 m1A Human chrX - 53394865 53394865 53394865 CCATTGCAGGGTAGCTCCCAGGGGGAGGACTCAGTGAGTGGTTCACAGAGAATTTCCAGTATCTA CCATTGCAGGGTAGCTCCCAGGGGGAGGACTCCGTGAGTGGTTCACAGAGAATTTCCAGTATCTA T G SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53394719..53396317 26863196 MeRIP-seq:(Medium) rs782788248 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_16390,Human_RBP_ID_92922,Human_RBP_ID_257110,Human_RBP_ID_736456,Human_RBP_ID_1062897,Human_RBP_ID_1716111,Human_RBP_ID_2075645,Human_RBP_ID_8008927,Human_RBP_ID_8936285,Human_RBP_ID_9317427,Human_RBP_ID_16904374,Human_RBP_ID_18152227,Human_RBP_ID_18414661,Human_RBP_ID_18545127,Human_RBP_ID_18921395,Human_RBP_ID_24346489,Human_RBP_ID_26362870,Human_RBP_ID_27794079 Human_Splice_Rec_2208841,Human_Splice_Rec_2208842,Human_Splice_Rec_2208890,Human_Splice_Rec_2208891,Human_Splice_Rec_2208904,Human_Splice_Rec_2208905 RMVar_hsa_circ_9378,RMVar_hsa_circ_59814,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_304627,RMVar_hsa_circ_50880,RMVar_hsa_circ_262491 98775 RMVar_ID_98775 Human_SNP_ID_717056446 m1A Human chrX - 53394878 53394877 53394878 TGACTCTCCGTTGCCATTGCAGGGTAGCTCCCAGGGGGAGGACTCAGTGAGTGGTTCACAGAGAA TGACTCTCCGTTGCCATTGCAGGGTAGCTCCC_GGGGGAGGACTCAGTGAGTGGTTCACAGAGAA CT C SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:53394828..53396508 32194978 MeRIP-seq:(Medium) rs1556887777 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16390,Human_RBP_ID_92922,Human_RBP_ID_257110,Human_RBP_ID_736456,Human_RBP_ID_967794,Human_RBP_ID_2075645,Human_RBP_ID_5083303,Human_RBP_ID_8008927,Human_RBP_ID_8936285,Human_RBP_ID_9317427,Human_RBP_ID_16904374,Human_RBP_ID_18152227,Human_RBP_ID_18414661,Human_RBP_ID_18545127,Human_RBP_ID_18921395,Human_RBP_ID_26362870,Human_RBP_ID_27834449 Human_Splice_Rec_2208841,Human_Splice_Rec_2208890,Human_Splice_Rec_2208904 RMVar_hsa_circ_9378,RMVar_hsa_circ_59814,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_304627,RMVar_hsa_circ_50880,RMVar_hsa_circ_262491 98776 RMVar_ID_98776 Human_SNP_ID_717056447 m1A Human chrX - 53394878 53394878 53394878 TGACTCTCCGTTGCCATTGCAGGGTAGCTCCCAGGGGGAGGACTCAGTGAGTGGTTCACAGAGAA TGACTCTCCGTTGCCATTGCAGGGTAGCTCCCCGGGGGAGGACTCAGTGAGTGGTTCACAGAGAA T G SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:53394828..53396508 32194978 MeRIP-seq:(Medium) rs1253991330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16390,Human_RBP_ID_92922,Human_RBP_ID_257110,Human_RBP_ID_736456,Human_RBP_ID_967794,Human_RBP_ID_2075645,Human_RBP_ID_5083303,Human_RBP_ID_8008927,Human_RBP_ID_8936285,Human_RBP_ID_9317427,Human_RBP_ID_16904374,Human_RBP_ID_18152227,Human_RBP_ID_18414661,Human_RBP_ID_18545127,Human_RBP_ID_18921395,Human_RBP_ID_26362870,Human_RBP_ID_27834449 Human_Splice_Rec_2208841,Human_Splice_Rec_2208890,Human_Splice_Rec_2208904 RMVar_hsa_circ_9378,RMVar_hsa_circ_59814,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_304627,RMVar_hsa_circ_50880,RMVar_hsa_circ_262491 98777 RMVar_ID_98777 Human_SNP_ID_717057968 m1A Human chrX + 53403635 53403635 53403635 CTTCCTCAAACTCCCGGATGTTGCGCACACCAATCTCCCGACAAAACTCTTCAAACACCTCATCC CTTCCTCAAACTCCCGGATGTTGCGCACACCAGTCTCCCGACAAAACTCTTCAAACACCTCATCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53403527..53403866 26863196 MeRIP-seq:(Medium) rs387906702 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_607 GWAS_ID_13059 98778 RMVar_ID_98778 Human_SNP_ID_717058293 m1A Human chrX - 53405353 53405353 53405353 GCACTGGATGGAACCCTATTCCAGAAGTCAGGAGTGATCTCTGGTGGGGCCAGTGACCTGAAGGC GCACTGGATGGAACCCTATTCCAGAAGTCAGGCGTGATCTCTGGTGGGGCCAGTGACCTGAAGGC T G SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53405226..53405352 26863196 MeRIP-seq:(Medium) rs1569356989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92934,Human_RBP_ID_736466,Human_RBP_ID_1062904,Human_RBP_ID_1342529,Human_RBP_ID_1716174,Human_RBP_ID_2075712,Human_RBP_ID_5637735,Human_RBP_ID_8009043,Human_RBP_ID_8720232,Human_RBP_ID_8936316,Human_RBP_ID_9316871,Human_RBP_ID_16904775,Human_RBP_ID_18921448,Human_RBP_ID_22841692,Human_RBP_ID_23142624,Human_RBP_ID_27794087 Human_Splice_Rec_2208828,Human_Splice_Rec_2208877 Human_miRNA_ID_2156594,Human_miRNA_ID_2160154,Human_miRNA_ID_2709422 RMVar_hsa_circ_9378,RMVar_hsa_circ_59814,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_66233,RMVar_hsa_circ_59215,RMVar_hsa_circ_72642,RMVar_hsa_circ_262494,RMVar_hsa_circ_330194,RMVar_hsa_circ_354775,RMVar_hsa_circ_354760,RMVar_hsa_circ_262493,RMVar_hsa_circ_312568,RMVar_hsa_circ_269505,RMVar_hsa_circ_286570,RMVar_hsa_circ_266506 98779 RMVar_ID_98779 Human_SNP_ID_717058370 m1A Human chrX - 53405781 53405781 53405781 GCGTGGGGAGCCTGAGACCTTCTTGCCTCTTGACTACCTGGAGGTGAGGCTTGTTGGGGATTGGG GCGTGGGGAGCCTGAGACCTTCTTGCCTCTTGGCTACCTGGAGGTGAGGCTTGTTGGGGATTGGG T C SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53405776..53405825 32194978 MeRIP-seq:(Medium) rs1252688371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_968989,Human_RBP_ID_5067557,Human_RBP_ID_5483653,Human_RBP_ID_8009049,Human_RBP_ID_8936328,Human_RBP_ID_9409227,Human_RBP_ID_19149250,Human_RBP_ID_24549905,Human_RBP_ID_26362591,Human_RBP_ID_27833854 Human_Splice_Rec_2208825,Human_Splice_Rec_2208874 Human_miRNA_ID_2169016,Human_miRNA_ID_2170539 RMVar_hsa_circ_9378,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_66233,RMVar_hsa_circ_59215,RMVar_hsa_circ_330194,RMVar_hsa_circ_354760,RMVar_hsa_circ_262493,RMVar_hsa_circ_266506 98780 RMVar_ID_98780 Human_SNP_ID_717059648 m1A Human chrX - 53412999 53412999 53412999 ACTGGCCTCAAAGAACAAGGAGATCGAGAAGGACAAGAAGCGTATGGACAAGGTGGAGGATGAAC ACTGGCCTCAAAGAACAAGGAGATCGAGAAGGTCAAGAAGCGTATGGACAAGGTGGAGGATGAAC T A SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:53412976..53413000 26863196 MeRIP-seq:(Medium) rs1556890763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92944,Human_RBP_ID_257127,Human_RBP_ID_1716208,Human_RBP_ID_2075733,Human_RBP_ID_3258942,Human_RBP_ID_3924447,Human_RBP_ID_5230841,Human_RBP_ID_5637743,Human_RBP_ID_8009118,Human_RBP_ID_8936344,Human_RBP_ID_9317444,Human_RBP_ID_16904942,Human_RBP_ID_17066128,Human_RBP_ID_17441784,Human_RBP_ID_18152253,Human_RBP_ID_18454489,Human_RBP_ID_18543105,Human_RBP_ID_18545129,Human_RBP_ID_18921491,Human_RBP_ID_22014048,Human_RBP_ID_22841698,Human_RBP_ID_23107643,Human_RBP_ID_24346553,Human_RBP_ID_24549920,Human_RBP_ID_24555726,Human_RBP_ID_26362915 Human_Splice_Rec_2208815,Human_Splice_Rec_2208864,Human_Splice_Rec_2208919 Human_miRNA_ID_2255848 RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_66233,RMVar_hsa_circ_59215,RMVar_hsa_circ_354760,RMVar_hsa_circ_72604,RMVar_hsa_circ_32872,RMVar_hsa_circ_358392 98781 RMVar_ID_98781 Human_SNP_ID_717063008 m1A Human chrX + 53431552 53431552 53431552 GGAAGGGCACTTGGCTGGCCAAGAAGTTGCACACTTTCTCTGGGAGGCTGGTCAGCAGTGGGGTG GGAAGGGCACTTGGCTGGCCAAGAAGTTGCACGCTTTCTCTGGGAGGCTGGTCAGCAGTGGGGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53431501..53431600 32194978 MeRIP-seq:(Medium) rs782541533 Functional Loss SNV dbSNP153 33..33 33 - - - 98782 RMVar_ID_98782 Human_SNP_ID_717063436 m1A Human chrX + 53433879 53433879 53433879 CCAGGCCCGAGGCTCCTCCGGTTATTACCGCCACCAGGCCCTGTCAAAAGGGACATGGTCAGGGT CCAGGCCCGAGGCTCCTCCGGTTATTACCGCCCCCAGGCCCTGTCAAAAGGGACATGGTCAGGGT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:53433671..53433914;chrX:53433701..53433924;chrX:53433690..53433918;chrX:53433701..53434179;chrX:53433666..53433906 26863196 MeRIP-seq:(Medium) rs12847788 Functional Loss SNV dbSNP153 33..33 33 - - - 98783 RMVar_ID_98783 Human_SNP_ID_717063539 m1A Human chrX - 53434245 53434244 53434246 GCCGGGACAGCGCGGCCGTGGAACTAGGAGAAAGAGATCGGTTTCGAGGGAAAGGGTCATGCTTA GCCGGGACAGCGCGGCCGTGGAACTAGGAGA__GAGATCGGTTTCGAGGGAAAGGGTCATGCTTA CTT C HSD17B10 Ensembl:ENSG00000072506 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53434243..53434375 26863196 MeRIP-seq:(Medium) rs1420315104 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8720289 Human_Splice_Rec_2209003 98784 RMVar_ID_98784 Human_SNP_ID_717084645 m1A Human chrX - 53547793 53547793 53547793 CCACTGCCGCCTCCACCACGCCCACACCCCCTACTGCACCCACCCCTGTCACTTCTGCTCCAGCC CCACTGCCGCCTCCACCACGCCCACACCCCCTGCTGCACCCACCCCTGTCACTTCTGCTCCAGCC T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53547742..53547870 26863196 MeRIP-seq:(Medium) rs1489173800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9317457,Human_RBP_ID_17096248,Human_RBP_ID_17328242,Human_RBP_ID_17442722,Human_RBP_ID_18963979,Human_RBP_ID_21837744,Human_RBP_ID_22123394,Human_RBP_ID_26306248,Human_RBP_ID_27149426,Human_RBP_ID_27382984 Human_miRNA_ID_2878421 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98785 RMVar_ID_98785 Human_SNP_ID_717084649 m1A Human chrX - 53547802 53547802 53547802 CCACCACCACCACTGCCGCCTCCACCACGCCCACACCCCCTACTGCACCCACCCCTGTCACTTCT CCACCACCACCACTGCCGCCTCCACCACGCCCTCACCCCCTACTGCACCCACCCCTGTCACTTCT T A HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chrX:53547676..53547907;chrX:53547751..53547999;chrX:53547751..53547825 26863196,32194978 MeRIP-seq:(Medium) rs201730836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277023,Human_RBP_ID_9317457,Human_RBP_ID_17096248,Human_RBP_ID_17328242,Human_RBP_ID_17442722,Human_RBP_ID_18963979,Human_RBP_ID_22123394,Human_RBP_ID_27382984,Human_RBP_ID_27552552 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98786 RMVar_ID_98786 Human_SNP_ID_717084653 m1A Human chrX - 53547839 53547806 53547839 GCTTCCTCCACCACCACTGCCACCTCAACCACATCTACCACCACCACCACTGCCGCCTCCACCAC GCTTCCTCCACCACCACTGCCACCTCAACCAC_________________________________ CGTGGTGGAGGCGGCAGTGGTGGTGGTGGTAGAT C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:53547739..53547904 26863410 MeRIP-seq:(Medium) rs782606145 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5067857,Human_RBP_ID_17326660,Human_RBP_ID_17441796,Human_RBP_ID_17554891,Human_RBP_ID_18522031,Human_RBP_ID_18963979,Human_RBP_ID_22123394,Human_RBP_ID_22425197,Human_RBP_ID_22841720,Human_RBP_ID_24555760,Human_RBP_ID_26306249,Human_RBP_ID_27382984,Human_RBP_ID_27552553 Human_miRNA_ID_2636233,Human_miRNA_ID_2638920 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98787 RMVar_ID_98787 Human_SNP_ID_717084657 m1A Human chrX + 53547814 53547814 53547814 GGTGGGTGCAGTAGGGGGTGTGGGCGTGGTGGAGGCGGCAGTGGTGGTGGTGGTAGATGTGGTTG GGTGGGTGCAGTAGGGGGTGTGGGCGTGGTGGCGGCGGCAGTGGTGGTGGTGGTAGATGTGGTTG A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:53547716..53547950 26863196 MeRIP-seq:(Medium) rs782126136 Functional Loss SNV dbSNP153 33..33 33 - - - 98788 RMVar_ID_98788 Human_SNP_ID_717084658 m1A Human chrX + 53547814 53547814 53547814 GGTGGGTGCAGTAGGGGGTGTGGGCGTGGTGGAGGCGGCAGTGGTGGTGGTGGTAGATGTGGTTG GGTGGGTGCAGTAGGGGGTGTGGGCGTGGTGGGGGCGGCAGTGGTGGTGGTGGTAGATGTGGTTG A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:53547716..53547950 26863196 MeRIP-seq:(Medium) rs782126136 Functional Loss SNV dbSNP153 33..33 33 - - - 98789 RMVar_ID_98789 Human_SNP_ID_717084670 m1A Human chrX - 53547839 53547839 53547839 GCTTCCTCCACCACCACTGCCACCTCAACCACATCTACCACCACCACCACTGCCGCCTCCACCAC GCTTCCTCCACCACCACTGCCACCTCAACCACGTCTACCACCACCACCACTGCCGCCTCCACCAC T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:53547739..53547904 26863410 MeRIP-seq:(Medium) rs1192210543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5067857,Human_RBP_ID_17326660,Human_RBP_ID_17441796,Human_RBP_ID_17554891,Human_RBP_ID_18522031,Human_RBP_ID_18963979,Human_RBP_ID_22123394,Human_RBP_ID_22425197,Human_RBP_ID_22841720,Human_RBP_ID_24555760,Human_RBP_ID_26306249,Human_RBP_ID_27382984,Human_RBP_ID_27552553 Human_miRNA_ID_2636233,Human_miRNA_ID_2638920 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98790 RMVar_ID_98790 Human_SNP_ID_717084681 m1A Human chrX - 53547891 53547891 53547891 TGCTCTCCCAGAAAACAAGGTGTCAGAAGCACAGGCTAATTCTGGCAGCGGTGCTTCCTCCACCA TGCTCTCCCAGAAAACAAGGTGTCAGAAGCACCGGCTAATTCTGGCAGCGGTGCTTCCTCCACCA T G HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:53547713..53547899 26863410 MeRIP-seq:(Medium) rs889765276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2075828,Human_RBP_ID_9339965,Human_RBP_ID_17328065,Human_RBP_ID_17441798,Human_RBP_ID_17554892,Human_RBP_ID_21837747,Human_RBP_ID_22468366,Human_RBP_ID_24555760,Human_RBP_ID_27382984 Human_miRNA_ID_2237974 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98791 RMVar_ID_98791 Human_SNP_ID_717084760 m1A Human chrX - 53548255 53548255 53548255 CCTTTTCCCGGCAGGTATTTCCCAGCCACTTCACACAGCAGCGGACCAAAGAAACAAACTGTGAG CCTTTTCCCGGCAGGTATTTCCCAGCCACTTCGCACAGCAGCGGACCAAAGAAACAAACTGTGAG T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53548205..53548278 26863196 MeRIP-seq:(Medium) rs1556925119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1062932,Human_RBP_ID_1716331,Human_RBP_ID_2075833,Human_RBP_ID_3977363,Human_RBP_ID_8720347,Human_RBP_ID_8936491,Human_RBP_ID_9265291,Human_RBP_ID_17327756,Human_RBP_ID_17441803,Human_RBP_ID_27834499 Human_Splice_Rec_2209014,Human_Splice_Rec_2209171,Human_Splice_Rec_2209333,Human_Splice_Rec_2209498 Human_miRNA_ID_2034742,Human_miRNA_ID_2036046,Human_miRNA_ID_2473778,Human_miRNA_ID_3108151 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 98792 RMVar_ID_98792 Human_SNP_ID_717085286 m1A Human chrX + 53551073 53551073 53551073 AACACACTGTCCTCCATATCCTCTAGGACACTACGGCGCAGGTCTGAGGGCAGAGTCTGGATGAA AACACACTGTCCTCCATATCCTCTAGGACACTGCGGCGCAGGTCTGAGGGCAGAGTCTGGATGAA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:53551026..53551100 26863196 MeRIP-seq:(Medium) rs112038748 Functional Loss SNV dbSNP153 33..33 33 - - - 98793 RMVar_ID_98793 Human_SNP_ID_717085296 m1A Human chrX - 53551148 53551148 53551148 CAGCAGAGAGCTGAGCAGCAGCGACGAGAACTAGCACAGAATGCCAGCTCAGACACCCCTATGGA CAGCAGAGAGCTGAGCAGCAGCGACGAGAACTGGCACAGAATGCCAGCTCAGACACCCCTATGGA T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:53551126..53551150 26863196 MeRIP-seq:(Medium) rs1409734658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93126,Human_RBP_ID_5637757,Human_RBP_ID_16905628 Human_Splice_Rec_2209165,Human_Splice_Rec_2209327,Human_Splice_Rec_2209492 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_126578,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_262526,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_16107,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533,RMVar_hsa_circ_108327,RMVar_hsa_circ_118170,RMVar_hsa_circ_86377,RMVar_hsa_circ_61097,RMVar_hsa_circ_262538,RMVar_hsa_circ_262539,RMVar_hsa_circ_262537,RMVar_hsa_circ_102446,RMVar_hsa_circ_269300,RMVar_hsa_circ_262540 98794 RMVar_ID_98794 Human_SNP_ID_717085603 m1A Human chrX + 53552689 53552689 53552689 CAGATTCCCCTGACCCATCACTCCTGCCTTGCACTTCCGCCACAGCTGGTGGGGCATCCCCAGGA CAGATTCCCCTGACCCATCACTCCTGCCTTGCCCTTCCGCCACAGCTGGTGGGGCATCCCCAGGA A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53552626..53552700 32194978 MeRIP-seq:(Medium) rs782233422 Functional Loss SNV dbSNP153 33..33 33 - - - 98795 RMVar_ID_98795 Human_SNP_ID_717085990 m1A Human chrX + 53554897 53554897 53554897 AGCTGCATCAGTTGAAGATGGGGTTGTTGGGTAGCTGTCAGGCATAGGCGTCCCATCTTTCTCGG AGCTGCATCAGTTGAAGATGGGGTTGTTGGGTGGCTGTCAGGCATAGGCGTCCCATCTTTCTCGG A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53554847..53554968 26863196 MeRIP-seq:(Medium) rs1436122562 Functional Loss SNV dbSNP153 33..33 33 - - - 98796 RMVar_ID_98796 Human_SNP_ID_717087025 m1A Human chrX - 53560350 53560350 53560350 CACCCATCCACTGATGGTGCGCCATGCAGACCACAGTTCTCTGACACTGGGCAGTGGCTCTTCAA CACCCATCCACTGATGGTGCGCCATGCAGACCGCAGTTCTCTGACACTGGGCAGTGGCTCTTCAA T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:53560301..53560350 32194978 MeRIP-seq:(Medium) rs1282250817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93142,Human_RBP_ID_2075878,Human_RBP_ID_8009385,Human_RBP_ID_8720373,Human_RBP_ID_8936585,Human_RBP_ID_17326691,Human_RBP_ID_17554921,Human_RBP_ID_18921663,Human_RBP_ID_21765632 Human_Splice_Rec_2209149,Human_Splice_Rec_2209311,Human_Splice_Rec_2209475 Human_miRNA_ID_2073378,Human_miRNA_ID_2075061,Human_miRNA_ID_2176175,Human_miRNA_ID_2179619,Human_miRNA_ID_3065221 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_262503,RMVar_hsa_circ_75758,RMVar_hsa_circ_49196,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_90734,RMVar_hsa_circ_262526,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_262530,RMVar_hsa_circ_127894,RMVar_hsa_circ_262532,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_127901,RMVar_hsa_circ_262542,RMVar_hsa_circ_262543,RMVar_hsa_circ_372073,RMVar_hsa_circ_378327,RMVar_hsa_circ_31763,RMVar_hsa_circ_262544,RMVar_hsa_circ_262545,RMVar_hsa_circ_265330,RMVar_hsa_circ_93940,RMVar_hsa_circ_109181,RMVar_hsa_circ_262546,RMVar_hsa_circ_124123,RMVar_hsa_circ_262548,RMVar_hsa_circ_45116,RMVar_hsa_circ_95244,RMVar_hsa_circ_262549,RMVar_hsa_circ_100342,RMVar_hsa_circ_262550,RMVar_hsa_circ_262551 98797 RMVar_ID_98797 Human_SNP_ID_717087033 m1A Human chrX - 53560397 53560397 53560397 ATTGTCCTTGCAGCAGACATCCCCCCATCCCCAGGAAATATCCCTACCACCCATCCACTGATGGT ATTGTCCTTGCAGCAGACATCCCCCCATCCCCGGGAAATATCCCTACCACCCATCCACTGATGGT T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53560282..53560464 26863196 MeRIP-seq:(Medium) rs1278255750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93142,Human_RBP_ID_847952,Human_RBP_ID_1071018,Human_RBP_ID_5535643,Human_RBP_ID_18921664,Human_RBP_ID_23103014,Human_RBP_ID_27552587 Human_Splice_Rec_2209149,Human_Splice_Rec_2209311,Human_Splice_Rec_2209475 Human_miRNA_ID_2041926,Human_miRNA_ID_2364888,Human_miRNA_ID_3020904 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_262503,RMVar_hsa_circ_75758,RMVar_hsa_circ_49196,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_90734,RMVar_hsa_circ_262526,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_262530,RMVar_hsa_circ_127894,RMVar_hsa_circ_262532,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_127901,RMVar_hsa_circ_262542,RMVar_hsa_circ_262543,RMVar_hsa_circ_372073,RMVar_hsa_circ_378327,RMVar_hsa_circ_31763,RMVar_hsa_circ_262544,RMVar_hsa_circ_262545,RMVar_hsa_circ_265330,RMVar_hsa_circ_93940,RMVar_hsa_circ_109181,RMVar_hsa_circ_262546,RMVar_hsa_circ_124123,RMVar_hsa_circ_262548,RMVar_hsa_circ_45116,RMVar_hsa_circ_95244,RMVar_hsa_circ_262549,RMVar_hsa_circ_100342,RMVar_hsa_circ_262550,RMVar_hsa_circ_262551 98798 RMVar_ID_98798 Human_SNP_ID_717087267 m1A Human chrX + 53561842 53561842 53561842 AGCGCTCAAATCGGACCAAGGGAGAAGCGTTCATATCAGGATAATCCTCATCCAATTCCATCTCA AGCGCTCAAATCGGACCAAGGGAGAAGCGTTCCTATCAGGATAATCCTCATCCAATTCCATCTCA A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:53561751..53561875 26863196 MeRIP-seq:(Medium) rs1407547671 Functional Loss SNV dbSNP153 33..33 33 - - - 98799 RMVar_ID_98799 Human_SNP_ID_717087268 m1A Human chrX + 53561842 53561842 53561842 AGCGCTCAAATCGGACCAAGGGAGAAGCGTTCATATCAGGATAATCCTCATCCAATTCCATCTCA AGCGCTCAAATCGGACCAAGGGAGAAGCGTTCGTATCAGGATAATCCTCATCCAATTCCATCTCA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:53561751..53561875 26863196 MeRIP-seq:(Medium) rs1407547671 Functional Loss SNV dbSNP153 33..33 33 - - - 98800 RMVar_ID_98800 Human_SNP_ID_717087432 m1A Human chrX - 53562839 53562839 53562839 CAACCTCAGCCAAGCTTCCACCTTGCAGGCCAACCGAGAAGGTGAGAGTGCCGAGGCCAGAAAGG CAACCTCAGCCAAGCTTCCACCTTGCAGGCCACCCGAGAAGGTGAGAGTGCCGAGGCCAGAAAGG T G HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:53562826..53562950 26863196 MeRIP-seq:(Medium) rs1043049048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257161,Human_RBP_ID_8936600,Human_RBP_ID_9409271,Human_RBP_ID_19148443,Human_RBP_ID_23103033,Human_RBP_ID_26362936,Human_RBP_ID_27149494 Human_Splice_Rec_2209143,Human_Splice_Rec_2209144,Human_Splice_Rec_2209305,Human_Splice_Rec_2209306,Human_Splice_Rec_2209469,Human_Splice_Rec_2209470 RMVar_hsa_circ_49196,RMVar_hsa_circ_104556,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_262524,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_262543,RMVar_hsa_circ_17855,RMVar_hsa_circ_31763,RMVar_hsa_circ_95244,RMVar_hsa_circ_262550,RMVar_hsa_circ_292102,RMVar_hsa_circ_44445,RMVar_hsa_circ_262554 98801 RMVar_ID_98801 Human_SNP_ID_717087567 m1A Human chrX + 53563710 53563710 53563710 AGAAAAAGGGTCCTCCCAAGAGAGACTGAGGCAAAGGAAGAGGCTATACTCAGTTCTGGGGCTCT AGAAAAAGGGTCCTCCCAAGAGAGACTGAGGCCAAGGAAGAGGCTATACTCAGTTCTGGGGCTCT A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53563706..53563856 26863196 MeRIP-seq:(Medium) rs1556943230 Functional Loss SNV dbSNP153 33..33 33 - - - 98802 RMVar_ID_98802 Human_SNP_ID_717099691 m1A Human chrX + 53625853 53625823 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCG______________________________GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG GGGACCAGGACCGGGGCCGGGGCCGGGGCCA G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs781866827 Functional Loss DEL dbSNP153 4..33 33 - - - 98803 RMVar_ID_98803 Human_SNP_ID_717099711 m1A Human chrX + 53625853 53625835 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCG__________________GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG GGGGCCGGGGCCGGGGCCA G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs1176817623 Functional Loss DEL dbSNP153 16..33 33 - - - 98804 RMVar_ID_98804 Human_SNP_ID_717099719 m1A Human chrX + 53625853 53625841 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCG____________GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG GGGGCCGGGGCCA G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs782399689 Functional Loss DEL dbSNP153 22..33 33 - - - 98805 RMVar_ID_98805 Human_SNP_ID_717099724 m1A Human chrX + 53625853 53625847 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCGGGGCCG______GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG GGGGCCA G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs782293841 Functional Loss DEL dbSNP153 28..33 33 - - - 98806 RMVar_ID_98806 Human_SNP_ID_717099730 m1A Human chrX + 53625853 53625852 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCGGGGCCGGGGCC_GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CA C RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs782050012 Functional Loss DEL dbSNP153 33..33 33 - - - 98807 RMVar_ID_98807 Human_SNP_ID_717099732 m1A Human chrX + 53625853 53625853 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG A G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs185693518 Functional Loss SNV dbSNP153 33..33 33 - - - 98808 RMVar_ID_98808 Human_SNP_ID_717099733 m1A Human chrX + 53625853 53625853 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCTGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG A T RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs185693518 Functional Loss SNV dbSNP153 33..33 33 - - - 98809 RMVar_ID_98809 Human_SNP_ID_717110487 m1A Human chrX - 53683970 53683970 53683970 GGTGGCTCGGTTACTGACTGCAGTAGCCGCGGAGGCGGCGGCAAGGTCTTCGGCTCGTGCCGTTC GGTGGCTCGGTTACTGACTGCAGTAGCCGCGGTGGCGGCGGCAAGGTCTTCGGCTCGTGCCGTTC T A HUWE1 Ensembl:ENSG00000086758 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chrX:53683926..53684000;chrX:53683925..53684084 26863196 MeRIP-seq:(Medium) rs969622328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5075831,Human_RBP_ID_8164788,Human_RBP_ID_8938792,Human_RBP_ID_9317529,Human_RBP_ID_18427951,Human_RBP_ID_22734263 Human_Splice_Rec_2209204,Human_Splice_Rec_2209659 98810 RMVar_ID_98810 Human_SNP_ID_717110492 m1A Human chrX - 53683981 53683981 53683981 GCGGAGGCGGCGGTGGCTCGGTTACTGACTGCAGTAGCCGCGGAGGCGGCGGCAAGGTCTTCGGC GCGGAGGCGGCGGTGGCTCGGTTACTGACTGCGGTAGCCGCGGAGGCGGCGGCAAGGTCTTCGGC T C HUWE1 Ensembl:ENSG00000086758 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53683965..53684105 26863196 MeRIP-seq:(Medium) rs1225166826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076150,Human_RBP_ID_8164788,Human_RBP_ID_8939249,Human_RBP_ID_9317529,Human_RBP_ID_18427853,Human_RBP_ID_22734263 98811 RMVar_ID_98811 Human_SNP_ID_717110922 m1A Human chrX + 53686333 53686333 53686333 CGCGCCGCCGGCAGCTGCCGGGCTGCCCCCGAAGATGCGGCTAGCTCTCCGCTGGCGCCTGCCGA CGCGCCGCCGGCAGCTGCCGGGCTGCCCCCGACGATGCGGCTAGCTCTCCGCTGGCGCCTGCCGA A C RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53686170..53686422 26863196 MeRIP-seq:(Medium) rs1339639435 Functional Loss SNV dbSNP153 33..33 33 - - - 98812 RMVar_ID_98812 Human_SNP_ID_717173633 m1A Human chrX - 54025659 54025659 54025659 CTGGGGGATGGTCATGAGAGTTGGTAGCTGAAATGGGAGTAGAGGTAACAGTCTCTGAAGATGAG CTGGGGGATGGTCATGAGAGTTGGTAGCTGAAGTGGGAGTAGAGGTAACAGTCTCTGAAGATGAG T C PHF8 Ensembl:ENSG00000172943 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:54025656..54025888 26863196 MeRIP-seq:(Medium) rs1378239759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848950 RMVar_hsa_circ_20102,RMVar_hsa_circ_95897,RMVar_hsa_circ_262587,RMVar_hsa_circ_112643,RMVar_hsa_circ_262592 98813 RMVar_ID_98813 Human_SNP_ID_717174791 m1A Human chrX + 54032393 54032389 54032393 CCCTTAACCTCAGCTTCTATTACTCTCCCCTCACTCACTCTGTTCCAATAGCATTGGACTGGACT CCCTTAACCTCAGCTTCTATTACTCTCCC____CTCACTCTGTTCCAATAGCATTGGACTGGACT CCTCA C RF00017-4706,RF00017-4501,RF00017-4484 RNACentral:URS0000954994,RNACentral:URS0000972B66,RNACentral:URS00009439B4 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:54032389..54032575 26863196 MeRIP-seq:(Medium) rs782766165 Functional Loss DEL dbSNP153 30..33 33 - - - 98814 RMVar_ID_98814 Human_SNP_ID_717177181 m1A Human chrX - 54043860 54043860 54043860 AGCTCCGCGGGCGTGGAGTCCTTGCAGCCCAAAGCATGAGGAGGTCCCTGTAGGATTCTGGACTG AGCTCCGCGGGCGTGGAGTCCTTGCAGCCCAACGCATGAGGAGGTCCCTGTAGGATTCTGGACTG T G PHF8 Ensembl:ENSG00000172943 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:54043815..54043902 26863196 MeRIP-seq:(Medium) rs1445701674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186944,Human_RBP_ID_2076230,Human_RBP_ID_3924811,Human_RBP_ID_5076153,Human_RBP_ID_16909731,Human_RBP_ID_23103351 Human_Splice_Rec_2209708,Human_Splice_Rec_2209750,Human_Splice_Rec_2209948 RMVar_hsa_circ_112643,RMVar_hsa_circ_262592 98815 RMVar_ID_98815 Human_SNP_ID_717244723 m1A Human chrX - 54443405 54443405 54443405 TCCAAGGAAGTCTTCCACCTCATCTAGCTCCAAGTCAGCTAAGTAGAAAAGGACAGGGCCCTTGG TCCAAGGAAGTCTTCCACCTCATCTAGCTCCAGGTCAGCTAAGTAGAAAAGGACAGGGCCCTTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:54443401..54443500 26863196 MeRIP-seq:(Medium) rs1398953747 Functional Loss SNV dbSNP153 33..33 33 - - - 98816 RMVar_ID_98816 Human_SNP_ID_717244821 m1A Human chrX - 54444108 54444108 54444108 TCTCTCTAGCTGTCTTAAGTGCAGTGGCTGTGACCTTGCATTTTCTCTGAGTGATGCAGGAGGCC TCTCTCTAGCTGTCTTAAGTGCAGTGGCTGTGGCCTTGCATTTTCTCTGAGTGATGCAGGAGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:54444001..54444200 26863196 MeRIP-seq:(Medium) rs779315411 Functional Loss SNV dbSNP153 33..33 33 - - - 98817 RMVar_ID_98817 Human_SNP_ID_717245110 m1A Human chrX - 54445693 54445690 54445694 TGGGGCCCCGACCCAGCCCTGCCTCCTCAGCCAGTGTCTTCACACGTACAACTCCACGTGGGGTG TGGGGCCCCGACCCAGCCCTGCCTCCTCAGC____GTCTTCACACGTACAACTCCACGTGGGGTG CACTG C FGD1 Ensembl:ENSG00000102302 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chrX:54445644..54445761;chrX:54445644..54445851 26863196 MeRIP-seq:(Medium) rs1163990990 Functional Loss DEL dbSNP153 32..35 33 - - - Human_miRNA_ID_338947,Human_miRNA_ID_472974,Human_miRNA_ID_478842,Human_miRNA_ID_795992,Human_miRNA_ID_848384,Human_miRNA_ID_1037619,Human_miRNA_ID_2333786,Human_miRNA_ID_2473782,Human_miRNA_ID_2477976,Human_miRNA_ID_2966871 RMVar_hsa_circ_95353,RMVar_hsa_circ_95448,RMVar_hsa_circ_262629,RMVar_hsa_circ_85876,RMVar_hsa_circ_262630,RMVar_hsa_circ_262628 98818 RMVar_ID_98818 Human_SNP_ID_717249411 m1A Human chrX - 54470641 54470641 54470641 CCGACCCCCGAGTGGCCAAGGGCCTGGCTCCCAGGGCAGAGGCCAGCCCCAGTTCTGCAGCAGTA CCGACCCCCGAGTGGCCAAGGGCCTGGCTCCCGGGGCAGAGGCCAGCCCCAGTTCTGCAGCAGTA T C FGD1 Ensembl:ENSG00000102302 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:54470626..54470775 26863196 MeRIP-seq:(Medium) rs1379164906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2210224 RMVar_hsa_circ_10454,RMVar_hsa_circ_95353,RMVar_hsa_circ_262630,RMVar_hsa_circ_24259,RMVar_hsa_circ_373651,RMVar_hsa_circ_37677,RMVar_hsa_circ_276799,RMVar_hsa_circ_262638,RMVar_hsa_circ_338149,RMVar_hsa_circ_262641,RMVar_hsa_circ_311100 98819 RMVar_ID_98819 Human_SNP_ID_717249437 m1A Human chrX - 54470709 54470709 54470709 CCTGCAGATGCCCCGGATGCCCCCCCCACTGGAGCCCATCCCCCCTCCACCATCACGCCCACTGC CCTGCAGATGCCCCGGATGCCCCCCCCACTGGGGCCCATCCCCCCTCCACCATCACGCCCACTGC T C FGD1 Ensembl:ENSG00000102302 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:54468871..54471423 26863196 MeRIP-seq:(Medium) rs1424577805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2210223 RMVar_hsa_circ_10454,RMVar_hsa_circ_95353,RMVar_hsa_circ_262630,RMVar_hsa_circ_24259,RMVar_hsa_circ_373651,RMVar_hsa_circ_37677,RMVar_hsa_circ_276799,RMVar_hsa_circ_262638,RMVar_hsa_circ_338149,RMVar_hsa_circ_262641,RMVar_hsa_circ_311100 98820 RMVar_ID_98820 Human_SNP_ID_717253862 m1A Human chrX - 54496016 54496016 54496016 TGAAGGCGAGCCCCGCAGCCCAAGCGCAGCGCACACGCGCGCCCCCGGCCACCGCCGTTCTCTCT TGAAGGCGAGCCCCGCAGCCCAAGCGCAGCGCGCACGCGCGCCCCCGGCCACCGCCGTTCTCTCT T C FGD1 Ensembl:ENSG00000102302 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:54495968..54496115 32194978 MeRIP-seq:(Medium) rs1171792357 Functional Loss SNV dbSNP153 33..33 33 - - - 98821 RMVar_ID_98821 Human_SNP_ID_717260092 m1A Human chrX + 54530381 54530381 54530381 TAGACGGCCGGGCAGTTAGGATCGTCTATTGGATGTGAAACCAGAGATGCCCGCCAACCTGGAAT TAGACGGCCGGGCAGTTAGGATCGTCTATTGGGTGTGAAACCAGAGATGCCCGCCAACCTGGAAT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:54530282..54530395 26863196 MeRIP-seq:(Medium) rs778904033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1716578,Human_RBP_ID_16910413,Human_RBP_ID_22631967 Human_Splice_Rec_2210423,Human_Splice_Rec_2210511,Human_Splice_Rec_2210541,Human_Splice_Rec_2210543 RMVar_hsa_circ_262642,RMVar_hsa_circ_121676 98822 RMVar_ID_98822 Human_SNP_ID_717262032 m1A Human chrX + 54541352 54541352 54541352 ACAAAAACGCAGGACCATTGAGAGCTACTGTCAGGATGTCCTAAGACGCCAGGAGGAGTTTGAGC ACAAAAACGCAGGACCATTGAGAGCTACTGTCGGGATGTCCTAAGACGCCAGGAGGAGTTTGAGC A G GNL3L Ensembl:ENSG00000130119 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:54541303..54541381 26863196 MeRIP-seq:(Medium) rs1186595519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93824,Human_RBP_ID_736736,Human_RBP_ID_2076268,Human_RBP_ID_8011081,Human_RBP_ID_16910714,Human_RBP_ID_18921986 Human_Splice_Rec_2210261,Human_Splice_Rec_2210262,Human_Splice_Rec_2210293,Human_Splice_Rec_2210294,Human_Splice_Rec_2210325,Human_Splice_Rec_2210326,Human_Splice_Rec_2210341,Human_Splice_Rec_2210342,Human_Splice_Rec_2210371,Human_Splice_Rec_2210372,Human_Splice_Rec_2210400,Human_Splice_Rec_2210401,Human_Splice_Rec_2210430,Human_Splice_Rec_2210431,Human_Splice_Rec_2210460,Human_Splice_Rec_2210461,Human_Splice_Rec_2210518,Human_Splice_Rec_2210519,Human_Splice_Rec_2210550,Human_Splice_Rec_2210551 RMVar_hsa_circ_89677,RMVar_hsa_circ_262643,RMVar_hsa_circ_101443,RMVar_hsa_circ_262644 98823 RMVar_ID_98823 Human_SNP_ID_717263418 m1A Human chrX - 54549232 54549232 54549232 TGTTTGTGGATCTGTATGTGTACTTAAGAGCTATGTGTATGTGTTCCTCTGTATCTACAGCCTTG TGTTTGTGGATCTGTATGTGTACTTAAGAGCTGTGTGTATGTGTTCCTCTGTATCTACAGCCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:54549223..54549362 26863196 MeRIP-seq:(Medium) rs1339094896 Functional Loss SNV dbSNP153 33..33 33 - - - 98824 RMVar_ID_98824 Human_SNP_ID_717264407 m1A Human chrX + 54554628 54554628 54554628 GGGTGACACGGACCCACTTGAAATGGAGATCAAGTTGCTCCATTCTCCGATGACGAAAATAGCAG GGGTGACACGGACCCACTTGAAATGGAGATCACGTTGCTCCATTCTCCGATGACGAAAATAGCAG A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1227010393 Functional Loss SNV dbSNP153 33..33 33 - - - 98825 RMVar_ID_98825 Human_SNP_ID_717265797 m1A Human chrX + 54562243 54562243 54562243 AGTTTTTGTATTTTTAGTAGAGACGATGTTTCACCATGTTGACCAGGCTGGTCTCGAACTCTTGA AGTTTTTGTATTTTTAGTAGAGACGATGTTTCGCCATGTTGACCAGGCTGGTCTCGAACTCTTGA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs758663708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 98826 RMVar_ID_98826 Human_SNP_ID_717265992 m1A Human chrX + 54563297 54563297 54563297 AAGCAGTATACATTCAGAATGCACCTCTACTTATGATGGGGCTACTTCCTGGTAAACCCATTGTA AAGCAGTATACATTCAGAATGCACCTCTACTTGTGATGGGGCTACTTCCTGGTAAACCCATTGTA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1387260594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3259774,Human_RBP_ID_5068947,Human_RBP_ID_8011209,Human_RBP_ID_16911202,Human_RBP_ID_17555015,Human_RBP_ID_18406067,Human_RBP_ID_24527082,Human_RBP_ID_26575102,Human_RBP_ID_27794248 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 98827 RMVar_ID_98827 Human_SNP_ID_717266058 m1A Human chrX + 54563647 54563643 54563648 CTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGTAGTCCCAGCTACCTA CTCTACCAAAAAAATACAAAGATTAGCTG_____GGTGTCTCATGCCTGTAGTCCCAGCTACCTA GGGCAT G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1177857776 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 98828 RMVar_ID_98828 Human_SNP_ID_717266059 m1A Human chrX + 54563647 54563647 54563647 CTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGTAGTCCCAGCTACCTA CTCTACCAAAAAAATACAAAGATTAGCTGGGCGTGGTGTCTCATGCCTGTAGTCCCAGCTACCTA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs909097527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 98829 RMVar_ID_98829 Human_SNP_ID_717352509 m1A Human chrX + 55000412 55000412 55000412 CGCCTAGGTTGGCGCGGGCTGGGAGGTGTTCCAGCCCTTTAAGATGTTGCGCGTGGTGAGCTGGA CGCCTAGGTTGGCGCGGGCTGGGAGGTGTTCCGGCCCTTTAAGATGTTGCGCGTGGTGAGCTGGA A G APEX2 Ensembl:ENSG00000169188 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:55000376..55000425 26863196 MeRIP-seq:(Medium) rs1466572734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5069088,Human_RBP_ID_5432247 98830 RMVar_ID_98830 Human_SNP_ID_717352521 m1A Human chrX - 55000426 55000426 55000426 AATCCCATTGATGTTCCAGCTCACCACGCGCAACATCTTAAAGGGCTGGAACACCTCCCAGCCCG AATCCCATTGATGTTCCAGCTCACCACGCGCATCATCTTAAAGGGCTGGAACACCTCCCAGCCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:55000376..55000525 26863196 MeRIP-seq:(Medium) rs760389136 Functional Loss SNV dbSNP153 33..33 33 - - - 98831 RMVar_ID_98831 Human_SNP_ID_717352522 m1A Human chrX - 55000426 55000426 55000426 AATCCCATTGATGTTCCAGCTCACCACGCGCAACATCTTAAAGGGCTGGAACACCTCCCAGCCCG AATCCCATTGATGTTCCAGCTCACCACGCGCAGCATCTTAAAGGGCTGGAACACCTCCCAGCCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:55000376..55000525 26863196 MeRIP-seq:(Medium) rs760389136 Functional Loss SNV dbSNP153 33..33 33 - - - 98832 RMVar_ID_98832 Human_SNP_ID_717353765 m1A Human chrX + 55007130 55007130 55007130 CTCCTGACATAGAGCTGCCTAGCCTACCACTGATGAGCGCCCTCATGACCCCGAAGACTCCAGAA CTCCTGACATAGAGCTGCCTAGCCTACCACTGGTGAGCGCCCTCATGACCCCGAAGACTCCAGAA A G APEX2 Ensembl:ENSG00000169188 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:55006900..55007229 26863196 MeRIP-seq:(Medium) rs143848599 Functional Loss SNV dbSNP153 33..33 33 - - - 98833 RMVar_ID_98833 Human_SNP_ID_717353855 m1A Human chrX + 55007385 55007385 55007385 TCTACATGTGTGCCAGGCCCCGGGGTCCTCCCACTGACCCCTCCTCCCGGTGCAACTTCTTCCTC TCTACATGTGTGCCAGGCCCCGGGGTCCTCCCCCTGACCCCTCCTCCCGGTGCAACTTCTTCCTC A C APEX2 Ensembl:ENSG00000169188 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:55007160..55007560 32194978 MeRIP-seq:(Medium) rs1480123345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22122820,Human_RBP_ID_27552754 98834 RMVar_ID_98834 Human_SNP_ID_717384732 m1A Human chrX - 55182010 55182010 55182010 GTGCAAAGGTAGCATAATCACTTGTTCCTTAAATAGGAACTTGTATGAATGACCACACGAGGGTT GTGCAAAGGTAGCATAATCACTTGTTCCTTAAGTAGGAACTTGTATGAATGACCACACGAGGGTT T C MTRNR2L10 Ensembl:ENSG00000256045 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1354439541 Functional Loss SNV dbSNP153 33..33 33 - - - 98835 RMVar_ID_98835 Human_SNP_ID_717483856 m1A Human chrX - 55728676 55728676 55728676 CAATAGCTCCATAACTCACCTCCCCACCAAAAAGCCTTACTCAATTTTACTTCATCCGACAGGCT CAATAGCTCCATAACTCACCTCCCCACCAAAAGGCCTTACTCAATTTTACTTCATCCGACAGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:55728658..55728823 26863196 MeRIP-seq:(Medium) rs1402258440 Functional Loss SNV dbSNP153 33..33 33 - - - 98836 RMVar_ID_98836 Human_SNP_ID_717692780 m1A Human chrX - 56563701 56563701 56563701 ATGAAGACTGCGGTTCCCTGGTCCTCCGGTGGAGAAAGGCCTGGGCGTAGGCCGCTGGCTGAGGT ATGAAGACTGCGGTTCCCTGGTCCTCCGGTGGTGAAAGGCCTGGGCGTAGGCCGCTGGCTGAGGT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:56563651..56563925 26863196 MeRIP-seq:(Medium) rs1478974222 Functional Loss SNV dbSNP153 33..33 33 - - - 98837 RMVar_ID_98837 Human_SNP_ID_717692807 m1A Human chrX - 56563803 56563803 56563803 GCGGGCGAAAGAGAGAGCGCGAGGGAAGGAGGAAGGAAGGAGGCACCGCCGCAGCGGGCTGGGCC GCGGGCGAAAGAGAGAGCGCGAGGGAAGGAGGCAGGAAGGAGGCACCGCCGCAGCGGGCTGGGCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:56563655..56563907 26863196 MeRIP-seq:(Medium) rs1002339016 Functional Loss SNV dbSNP153 33..33 33 - - - 98838 RMVar_ID_98838 Human_SNP_ID_717692815 m1A Human chrX - 56563820 56563818 56563820 GGGCAGGGAAGGCGCGGGCGGGCGAAAGAGAGAGCGCGAGGGAAGGAGGAAGGAAGGAGGCACCG GGGCAGGGAAGGCGCGGGCGGGCGAAAGAGAG__CGCGAGGGAAGGAGGAAGGAAGGAGGCACCG GCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:56563612..56564000 26863196 MeRIP-seq:(Medium) rs1057515975 Functional Loss DEL dbSNP153 33..34 33 - - - Clinvar_Rec_608 98839 RMVar_ID_98839 Human_SNP_ID_717734345 m1A Human chrX + 56729364 56729364 56729364 ACGACCCGTTTCTGTAATCCTTATGGGAGACCAACCTTGTGCCTCCGGGAGATCCACTCTCCCAC ACGACCCGTTTCTGTAATCCTTATGGGAGACCGACCTTGTGCCTCCGGGAGATCCACTCTCCCAC A G NBDY Ensembl:ENSG00000204272 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:56729313..56729533 26863196 MeRIP-seq:(Medium) rs1013236536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736992,Human_RBP_ID_1716709,Human_RBP_ID_5076171,Human_RBP_ID_8720800,Human_RBP_ID_18922129,Human_RBP_ID_24347770 Human_miRNA_ID_2477039,Human_miRNA_ID_2942918,Human_miRNA_ID_2962823 RMVar_hsa_circ_118261,RMVar_hsa_circ_262678 98840 RMVar_ID_98840 Human_SNP_ID_717737654 m1A Human chrX - 56748843 56748843 56748843 TTATCCTCCATTCTCATCCCATCTCGTATGCCAGCTACCCTCAACTTGGCACTTCCTAGTAACTC TTATCCTCCATTCTCATCCCATCTCGTATGCCGGCTACCCTCAACTTGGCACTTCCTAGTAACTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:56748841..56748949 26863196 MeRIP-seq:(Medium) rs868787841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1231107,Human_RBP_ID_3925173 98841 RMVar_ID_98841 Human_SNP_ID_717824443 m1A Human chrX - 57119510 57119508 57119511 AAGAACCTTAGAAGAGGTCCAGAGTAAAGAGGAGAAGGATCAACCTGACAGGGTCTGTGGAGAGG AAGAACCTTAGAAGAGGTCCAGAGTAAAGAG___AAGGATCAACCTGACAGGGTCTGTGGAGAGG TCTC T SPIN2B Ensembl:ENSG00000186787 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:57119355..57119588 26863196 MeRIP-seq:(Medium) rs1439635570 Functional Loss DEL dbSNP153 32..34 33 - - - 98842 RMVar_ID_98842 Human_SNP_ID_717824732 m1A Human chrX - 57121128 57121128 57121128 GCCAGGCAAGGGTGGGGTGGGGGAGTGCGGTGAGCAACATGAAAAGGGGGTAGGAACGGGAGCCA GCCAGGCAAGGGTGGGGTGGGGGAGTGCGGTGGGCAACATGAAAAGGGGGTAGGAACGGGAGCCA T C SPIN2B Ensembl:ENSG00000186787 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:57121013..57121150 26863196 MeRIP-seq:(Medium) rs774736715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16149,Human_RBP_ID_8226570,Human_RBP_ID_9443174,Human_RBP_ID_22122824,Human_RBP_ID_26363883 98843 RMVar_ID_98843 Human_SNP_ID_717944531 m1A Human chrX + 57592169 57592169 57592169 GAGGCCCTGACTCGCCGGCTGGCCAGGTCCCCACGCGCCGCCTCCTGCTGCTCCGGGGCCCCCAA GAGGCCCTGACTCGCCGGCTGGCCAGGTCCCCCCGCGCCGCCTCCTGCTGCTCCGGGGCCCCCAA A C ZXDB Ensembl:ENSG00000198455 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:57592151..57592350 26863196 MeRIP-seq:(Medium) rs1427159020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5069360 98844 RMVar_ID_98844 Human_SNP_ID_717944584 m1A Human chrX + 57592280 57592280 57592280 GGGGCCCTGGCCCAAGCCTGTTGGCGCCGAGGACCGATCAACCTAGCGGCGGCGGCGGCGGCGGC GGGGCCCTGGCCCAAGCCTGTTGGCGCCGAGGCCCGATCAACCTAGCGGCGGCGGCGGCGGCGGC A C ZXDB Ensembl:ENSG00000198455 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chrX:57592151..57592325;chrX:57592170..57592313 26863196 MeRIP-seq:(Medium) rs771783102 Functional Loss SNV dbSNP153 33..33 33 - - - 98845 RMVar_ID_98845 Human_SNP_ID_717944806 m1A Human chrX + 57592707 57592707 57592707 CGCCCCGCAAGCTGGGTTCCCGCATGCCGCGCACCCGGGTGACTGCCCAGAGCTGCCGCCAGACC CGCCCCGCAAGCTGGGTTCCCGCATGCCGCGCCCCCGGGTGACTGCCCAGAGCTGCCGCCAGACC A C ZXDB Ensembl:ENSG00000198455 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:57592626..57592878 26863196 MeRIP-seq:(Medium) rs750114140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076643,Human_RBP_ID_8720909 98846 RMVar_ID_98846 Human_SNP_ID_508788234 m1A Human chr12 - 82358235 82358235 82358235 GGCGGCCTAACCACCCGCAAGCCTTCGTGGGGAGCGTTCGCGAGGGTATGTAAGAAGGCAACCAT GGCGGCCTAACCACCCGCAAGCCTTCGTGGGGGGCGTTCGCGAGGGTATGTAAGAAGGCAACCAT T C CCDC59 Ensembl:ENSG00000133773 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:82358201..82358348 26863196 MeRIP-seq:(Medium) rs1182579291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755270,Human_RBP_ID_9366719,Human_RBP_ID_22039473,Human_RBP_ID_26321804,Human_RBP_ID_27805780,Human_RBP_ID_27836779 Human_Splice_Rec_1404713,Human_Splice_Rec_1404719,Human_Splice_Rec_1404735,Human_Splice_Rec_1404737 98847 RMVar_ID_98847 Human_SNP_ID_508788306 m1A Human chr12 + 82358338 82358338 82358338 GTGGAAACCCCTTCACCACGCGCCTCAATACCACCAGGCCGCCACTTCGCGGACCGCCTCACCGG GTGGAAACCCCTTCACCACGCGCCTCAATACCGCCAGGCCGCCACTTCGCGGACCGCCTCACCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:82358261..82358375;chr12:82358226..82358375;chr12:82358251..82358375 26863196 MeRIP-seq:(Medium) rs773800297 Functional Loss SNV dbSNP153 33..33 33 - - - 98848 RMVar_ID_98848 Human_SNP_ID_508788315 m1A Human chr12 + 82358349 82358349 82358349 TTCACCACGCGCCTCAATACCACCAGGCCGCCACTTCGCGGACCGCCTCACCGGCGCCATTGCAG TTCACCACGCGCCTCAATACCACCAGGCCGCCCCTTCGCGGACCGCCTCACCGGCGCCATTGCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:82358201..82358375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 98849 RMVar_ID_98849 Human_SNP_ID_508788581 m1A Human chr12 + 82358755 82358755 82358755 TGCCACCGGAGACAGTGCTGGCTGCGCTGAGGAAGTCAGCGTCGGAGACGGAGGCCCTGCCCTCA TGCCACCGGAGACAGTGCTGGCTGCGCTGAGGGAGTCAGCGTCGGAGACGGAGGCCCTGCCCTCA A G METTL25 Ensembl:ENSG00000127720 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:82358550..82358894 26863196 MeRIP-seq:(Medium) rs374622914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1404739,Human_Splice_Rec_1404745,Human_Splice_Rec_1404763,Human_Splice_Rec_1404785 98850 RMVar_ID_98850 Human_SNP_ID_509671714 m1A Human chr12 - 85836302 85836302 85836302 CTGAAAGCCAGGAACATCCGAGGAGAAGAGAAAGCTTCCAGCCCTCCTCCCTTCACCCTGGAAAT CTGAAAGCCAGGAACATCCGAGGAGAAGAGAACGCTTCCAGCCCTCCTCCCTTCACCCTGGAAAT T G RASSF9 Ensembl:ENSG00000198774 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:85836251..85836358 26863196 MeRIP-seq:(Medium) rs1428861874 Functional Loss SNV dbSNP153 33..33 33 - - - 98851 RMVar_ID_98851 Human_SNP_ID_510249764 m1A Human chr12 + 88142030 88142030 88142030 CGGACTCTGGGTCCAGCCAAATGGTCCCGAGCAAGCCAAAGCGGCAGCGGCTGCTAGGCGACACC CGGACTCTGGGTCCAGCCAAATGGTCCCGAGCCAGCCAAAGCGGCAGCGGCTGCTAGGCGACACC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:88141903..88142056 26863196 MeRIP-seq:(Medium) rs1372247358 Functional Loss SNV dbSNP153 33..33 33 - - - 98852 RMVar_ID_98852 Human_SNP_ID_510262280 m1A Human chr12 + 88196237 88196237 88196237 CATGACATGTTAGCTTGAGAATGTATTTTCATAATTGTATACTTGTTTTTAACTTTAAATGTAAT CATGACATGTTAGCTTGAGAATGTATTTTCATGATTGTATACTTGTTTTTAACTTTAAATGTAAT A G TMTC3 Ensembl:ENSG00000139324 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12825549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2359686,Human_RBP_ID_6229516,Human_RBP_ID_12049369,Human_RBP_ID_18264871,Human_RBP_ID_27634480 GWAS_ID_13060,GWAS_ID_13061,GWAS_ID_13062,GWAS_ID_13063,GWAS_ID_13064,GWAS_ID_13065,GWAS_ID_13066 RMVar_hsa_circ_83502,RMVar_hsa_circ_94272,RMVar_hsa_circ_158658,RMVar_hsa_circ_158669,RMVar_hsa_circ_158667,RMVar_hsa_circ_116776 98853 RMVar_ID_98853 Human_SNP_ID_510353266 m1A Human chr12 - 88580425 88580425 88580425 CTCGCGCCGAGACTAGAAGCGCTGCGGGAAGCAGGGACAGTGGAGAGGGCGCTGCGCTCGGGCTA CTCGCGCCGAGACTAGAAGCGCTGCGGGAAGCGGGGACAGTGGAGAGGGCGCTGCGCTCGGGCTA T C KITLG Ensembl:ENSG00000049130 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:88580401..88580475 26863196 MeRIP-seq:(Medium) rs574646451 Functional Loss SNV dbSNP153 33..33 33 - - - 98854 RMVar_ID_98854 Human_SNP_ID_510353356 m1A Human chr12 + 88580608 88580608 88580608 GCGGAGGGAAGAATCGGGAGGGCGGCCAGAGCACGGTAAATGCCCCAGAAGTTTGGCAGATTAGG GCGGAGGGAAGAATCGGGAGGGCGGCCAGAGCGCGGTAAATGCCCCAGAAGTTTGGCAGATTAGG A G AC024941.2 Ensembl:ENSG00000281333 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:88580579..88582093 26863196 MeRIP-seq:(Medium) rs1349029916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1406307 98855 RMVar_ID_98855 Human_SNP_ID_510560725 m1A Human chr12 + 89437126 89437122 89437126 TCTTCATCCCCTATGCTACAGCACTCGATCAGACAGTTGTCACCTCATGTCTGGATTACTATTAC TCTTCATCCCCTATGCTACAGCACTCGAT____CAGTTGTCACCTCATGTCTGGATTACTATTAC TCAGA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:89437090..89437260 26863196 MeRIP-seq:(Medium) rs1235073024 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_158685 98856 RMVar_ID_98856 Human_SNP_ID_510581571 m1A Human chr12 - 89525322 89525322 89525322 GTGGGCTGCTGCCCGGCCCCGCCGCCCAGCCAAGCCGCCGCCTGGGTGGCCATTCCCAAGCCGGA GTGGGCTGCTGCCCGGCCCCGCCGCCCAGCCAGGCCGCCGCCTGGGTGGCCATTCCCAAGCCGGA T C POC1B-GALNT4,POC1B Ensembl:ENSG00000259075,Ensembl:ENSG00000139323 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:89525317..89525408 26863196 MeRIP-seq:(Medium) rs1430746855 Functional Loss SNV dbSNP153 33..33 33 - - - 98857 RMVar_ID_98857 Human_SNP_ID_510581856 m1A Human chr12 + 89525970 89525970 89525970 CGGAGAGGGGAGGGGAGAGGATGGGGAAGGAGAGGGGACCGTGCGGCTCCCGGAACCGTCTGCCC CGGAGAGGGGAGGGGAGAGGATGGGGAAGGAGCGGGGACCGTGCGGCTCCCGGAACCGTCTGCCC A C POC1B-AS1 Ensembl:ENSG00000270344 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:89525922..89526026 26863196 MeRIP-seq:(Medium) rs1321312059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8179703 98858 RMVar_ID_98858 Human_SNP_ID_510581857 m1A Human chr12 + 89525970 89525970 89525970 CGGAGAGGGGAGGGGAGAGGATGGGGAAGGAGAGGGGACCGTGCGGCTCCCGGAACCGTCTGCCC CGGAGAGGGGAGGGGAGAGGATGGGGAAGGAGGGGGGACCGTGCGGCTCCCGGAACCGTCTGCCC A G POC1B-AS1 Ensembl:ENSG00000270344 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:89525922..89526026 26863196 MeRIP-seq:(Medium) rs1321312059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8179703 98859 RMVar_ID_98859 Human_SNP_ID_510586529 m1A Human chr12 + 89545432 89545432 89545432 AATCCTGACTTCCTCCTCCCAGCACTCGTTCCATAATTCTTTACCCTCACCTAGCATCTTGACAG AATCCTGACTTCCTCCTCCCAGCACTCGTTCCGTAATTCTTTACCCTCACCTAGCATCTTGACAG A G POC1B-AS1 Ensembl:ENSG00000270344 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:89545392..89545519 26863196 MeRIP-seq:(Medium) rs1021612292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3416266 98860 RMVar_ID_98860 Human_SNP_ID_510604746 m1A Human chr12 + 89626577 89626577 89626577 TTCATCACCATCTCCACCTTCTTCACTCTTCAATGGCTGCATTTCCATGGCTGCACCATCCTGGG TTCATCACCATCTCCACCTTCTTCACTCTTCAGTGGCTGCATTTCCATGGCTGCACCATCCTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:89626526..89626678 26863196 MeRIP-seq:(Medium) rs1255020721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158698 98861 RMVar_ID_98861 Human_SNP_ID_510624981 m1A Human chr12 + 89708374 89708374 89708374 GCGACTCCCAGACTGACCCGGCGCTGAGGTGCACGGCGAGAAGCCCGCTCACCTTCACAATCTCC GCGACTCCCAGACTGACCCGGCGCTGAGGTGCGCGGCGAGAAGCCCGCTCACCTTCACAATCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:89708373..89708795 26863196 MeRIP-seq:(Medium) rs936258201 Functional Loss SNV dbSNP153 33..33 33 - - - 98862 RMVar_ID_98862 Human_SNP_ID_510625139 m1A Human chr12 - 89708803 89708803 89708803 GTGCAGCGTGAGTAGGGAGCCCCGGCTGGTGGACGCCGAGCCTCTCGGCTCCTTGGCCGCCCCAT GTGCAGCGTGAGTAGGGAGCCCCGGCTGGTGGGCGCCGAGCCTCTCGGCTCCTTGGCCGCCCCAT T C ATP2B1 Ensembl:ENSG00000070961 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:89708601..89708825 26863196 MeRIP-seq:(Medium) rs1264836072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229683,Human_RBP_ID_810112,Human_RBP_ID_4243872,Human_RBP_ID_5462215,Human_RBP_ID_18457072 98863 RMVar_ID_98863 Human_SNP_ID_510625668 m1A Human chr12 + 89709833 89709833 89709833 CTGTTTCGGCGCGGGGCCGGGCCGCTGCCGCGACGTGTGGAGGCAGGAGAGCGATGATTGCCGCA CTGTTTCGGCGCGGGGCCGGGCCGCTGCCGCGGCGTGTGGAGGCAGGAGAGCGATGATTGCCGCA A G ATP2B1-AS1 Ensembl:ENSG00000271614 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:89709754..89710103;chr12:89709786..89710004 26863196 MeRIP-seq:(Medium) rs924534094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087460 98864 RMVar_ID_98864 Human_SNP_ID_710465524 m1A Human chrX + 15688611 15688611 15688611 GGGTCTCCAGAAGTGGAATTGCCTCATGTGTGATGCTAGATAGTAGACAGTCTTGATAATAGCCT GGGTCTCCAGAAGTGGAATTGCCTCATGTGTGTTGCTAGATAGTAGACAGTCTTGATAATAGCCT A T CA5BP1 Ensembl:ENSG00000186312 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:15688608..15688673 26863196 MeRIP-seq:(Medium) rs1272444263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261412,RMVar_hsa_circ_117753 98865 RMVar_ID_98865 Human_SNP_ID_710467637 m1A Human chrX + 15700755 15700755 15700755 TGACATTGAGGGCAGATCATTCTTGGTTGTGGAGACTGTCCTGTGCATTGCAGGATGTTTAATTG TGACATTGAGGGCAGATCATTCTTGGTTGTGGGGACTGTCCTGTGCATTGCAGGATGTTTAATTG A G CA5B,CA5BP1 Ensembl:ENSG00000169239,Ensembl:ENSG00000186312 Protein coding,Pseudogene intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs5936018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18408356 GWAS_ID_13067,GWAS_ID_13068,GWAS_ID_13069,GWAS_ID_13070,GWAS_ID_13071 98866 RMVar_ID_98866 Human_SNP_ID_710467638 m1A Human chrX + 15700755 15700755 15700755 TGACATTGAGGGCAGATCATTCTTGGTTGTGGAGACTGTCCTGTGCATTGCAGGATGTTTAATTG TGACATTGAGGGCAGATCATTCTTGGTTGTGGTGACTGTCCTGTGCATTGCAGGATGTTTAATTG A T CA5B,CA5BP1 Ensembl:ENSG00000169239,Ensembl:ENSG00000186312 Protein coding,Pseudogene intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs5936018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18408356 GWAS_ID_13067,GWAS_ID_13068,GWAS_ID_13069,GWAS_ID_13070,GWAS_ID_13071 98867 RMVar_ID_98867 Human_SNP_ID_710486006 m1A Human chrX - 15799905 15799905 15799905 GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATAAAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATATAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:15790997..15801324 26863196 MeRIP-seq:(Medium) rs201893706 Functional Loss SNV dbSNP153 33..33 33 - - - 98868 RMVar_ID_98868 Human_SNP_ID_710486007 m1A Human chrX - 15799905 15799905 15799905 GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATAAAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATAGAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:15790997..15801324 26863196 MeRIP-seq:(Medium) rs201893706 Functional Loss SNV dbSNP153 33..33 33 - - - 98869 RMVar_ID_98869 Human_SNP_ID_710486008 m1A Human chrX - 15799905 15799905 15799905 GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATAAAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT GCTTCTCTTCTTCTAGTTGTTGTTCTTCAATACAAGTGTCCTCCTCTTCCTCCTTCTGTGAGAGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:15790997..15801324 26863196 MeRIP-seq:(Medium) rs201893706 Functional Loss SNV dbSNP153 33..33 33 - - - 98870 RMVar_ID_98870 Human_SNP_ID_710486715 m1A Human chrX + 15803784 15803782 15803785 AAGGAAAAGGAAGAGGCGGCTAAAAAACGGCAAGAAGAACAAGAGGTATGGTAGGAATCACGTAA AAGGAAAAGGAAGAGGCGGCTAAAAAACGGC___AAGAACAAGAGGTATGGTAGGAATCACGTAA CAAG C ZRSR2 Ensembl:ENSG00000169249 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chrX:15803714..15808262;chrX:15803633..15808262 26863196 MeRIP-seq:(Medium) rs760370515 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_24549892 Human_Splice_Rec_2188035,Human_Splice_Rec_2188036,Human_Splice_Rec_2188055 RMVar_hsa_circ_364264 98871 RMVar_ID_98871 Human_SNP_ID_710486716 m1A Human chrX + 15803783 15803783 15803783 GAAGGAAAAGGAAGAGGCGGCTAAAAAACGGCAAGAAGAACAAGAGGTATGGTAGGAATCACGTA GAAGGAAAAGGAAGAGGCGGCTAAAAAACGGCCAGAAGAACAAGAGGTATGGTAGGAATCACGTA A C ZRSR2 Ensembl:ENSG00000169249 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:15803641..15808262;chrX:15803633..15808262 26863196 MeRIP-seq:(Medium) rs1299665122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24549892 Human_Splice_Rec_2188035,Human_Splice_Rec_2188036,Human_Splice_Rec_2188055 RMVar_hsa_circ_364264 98872 RMVar_ID_98872 Human_SNP_ID_710489954 m1A Human chrX + 15823057 15823057 15823057 CATCAAAGAGTCGGGAGAGGCACAATTCACGAAGCAGAGGAAGAAATAGGGACCGCAGCAGGGAC CATCAAAGAGTCGGGAGAGGCACAATTCACGAGGCAGAGGAAGAAATAGGGACCGCAGCAGGGAC A G ZRSR2 Ensembl:ENSG00000169249 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:15822976..15823181;chrX:15822928..15823182 26863196 MeRIP-seq:(Medium) rs1181530002 Functional Loss SNV dbSNP153 33..33 33 - - - 98873 RMVar_ID_98873 Human_SNP_ID_710489966 m1A Human chrX + 15823081 15823081 15823081 ATTCACGAAGCAGAGGAAGAAATAGGGACCGCAGCAGGGACCGCAGCCGGGGCCGGGGCAGCCGG ATTCACGAAGCAGAGGAAGAAATAGGGACCGCGGCAGGGACCGCAGCCGGGGCCGGGGCAGCCGG A G ZRSR2 Ensembl:ENSG00000169249 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:15823030..15823187 26863196 MeRIP-seq:(Medium) rs777453990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26362681 98874 RMVar_ID_98874 Human_SNP_ID_710494781 m1A Human chrX - 15854756 15854756 15854756 GCACCACGGCTTCTCTTCCTCAGCACGGCGACAGGGGCTTCCCCTTCGCCGCCGCCGCCGCCGCC GCACCACGGCTTCTCTTCCTCAGCACGGCGACGGGGGCTTCCCCTTCGCCGCCGCCGCCGCCGCC T C AP1S2 Ensembl:ENSG00000182287 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:15854685..15854776 26863196 MeRIP-seq:(Medium) rs1272053248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_732417,Human_RBP_ID_5076030 Human_Splice_Rec_2188056,Human_Splice_Rec_2188066,Human_Splice_Rec_2188092,Human_Splice_Rec_2188104,Human_Splice_Rec_2188125,Human_Splice_Rec_2188133,Human_Splice_Rec_2188141,Human_Splice_Rec_2188151 98875 RMVar_ID_98875 Human_SNP_ID_710642444 m1A Human chrX - 16719676 16719676 16719676 CGCCGCGGTCCCGATCCCCAGAGACCGCAGCGAGCACTGGTTGCCTTTGACTCCACTCTGCGCGA CGCCGCGGTCCCGATCCCCAGAGACCGCAGCGCGCACTGGTTGCCTTTGACTCCACTCTGCGCGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:16719626..16719875 26863196 MeRIP-seq:(Medium) rs771902156 Functional Loss SNV dbSNP153 33..33 33 - - - 98876 RMVar_ID_98876 Human_SNP_ID_710642455 m1A Human chrX - 16719695 16719695 16719695 CATCCCGCTCGCGGGCCGCCGCCGCGGTCCCGATCCCCAGAGACCGCAGCGAGCACTGGTTGCCT CATCCCGCTCGCGGGCCGCCGCCGCGGTCCCGGTCCCCAGAGACCGCAGCGAGCACTGGTTGCCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:16719626..16719825 26863196 MeRIP-seq:(Medium) rs776473927 Functional Loss SNV dbSNP153 33..33 33 - - - 98877 RMVar_ID_98877 Human_SNP_ID_710642456 m1A Human chrX - 16719695 16719695 16719695 CATCCCGCTCGCGGGCCGCCGCCGCGGTCCCGATCCCCAGAGACCGCAGCGAGCACTGGTTGCCT CATCCCGCTCGCGGGCCGCCGCCGCGGTCCCGCTCCCCAGAGACCGCAGCGAGCACTGGTTGCCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:16719626..16719825 26863196 MeRIP-seq:(Medium) rs776473927 Functional Loss SNV dbSNP153 33..33 33 - - - 98878 RMVar_ID_98878 Human_SNP_ID_710642472 m1A Human chrX - 16719750 16719750 16719750 GCCCACCGCCTGCCACCGGCTGCTGCAAGCCCAACCAACTGCTCAAGCCCCGGAACATCCCGCTC GCCCACCGCCTGCCACCGGCTGCTGCAAGCCCGACCAACTGCTCAAGCCCCGGAACATCCCGCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:16719701..16736177 32194978 MeRIP-seq:(Medium) rs1328256122 Functional Loss SNV dbSNP153 33..33 33 - - - 98879 RMVar_ID_98879 Human_SNP_ID_710642499 m1A Human chrX - 16719829 16719829 16719829 CCCGCTTGCTGCAGCTCCTCCTCCGCAGACTCAGCCACCGTCTCGGACGGCTGCTCGGGTGGAGC CCCGCTTGCTGCAGCTCCTCCTCCGCAGACTCGGCCACCGTCTCGGACGGCTGCTCGGGTGGAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:16719676..16719900 32194978 MeRIP-seq:(Medium) rs780793308 Functional Loss SNV dbSNP153 33..33 33 - - - 98880 RMVar_ID_98880 Human_SNP_ID_710651785 m1A Human chrX - 16771731 16771731 16771731 GTTCTGCTACCTACACTGCATTGTAGTGGTACAAATATGGCTCGCTGTAGCCTCGGCCTCCTGGG GTTCTGCTACCTACACTGCATTGTAGTGGTACGAATATGGCTCGCTGTAGCCTCGGCCTCCTGGG T C lnc-CTPS2-8 RNACentral:URS0000D5A320 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:16771682..16771779 26863196 MeRIP-seq:(Medium) rs900267206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7989483,Human_RBP_ID_16856128,Human_RBP_ID_18917755 98881 RMVar_ID_98881 Human_SNP_ID_710654965 m1A Human chrX + 16786828 16786828 16786828 TTTGGCGGCGCGCGGCGGGGAAGCCGGGAGGGAGGGCAGGGGGCGCACGCGGTTCTAAGGGAGAA TTTGGCGGCGCGCGGCGGGGAAGCCGGGAGGGGGGGCAGGGGGCGCACGCGGTTCTAAGGGAGAA A G TXLNG Ensembl:ENSG00000086712 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:16786824..16787086 26863196 MeRIP-seq:(Medium) rs1408981735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930579,Human_RBP_ID_8226480,Human_RBP_ID_18468290,Human_RBP_ID_21997242,Human_RBP_ID_26796979 98882 RMVar_ID_98882 Human_SNP_ID_710654966 m1A Human chrX + 16786833 16786833 16786833 CGGCGCGCGGCGGGGAAGCCGGGAGGGAGGGCAGGGGGCGCACGCGGTTCTAAGGGAGAAGGGGT CGGCGCGCGGCGGGGAAGCCGGGAGGGAGGGCGGGGGGCGCACGCGGTTCTAAGGGAGAAGGGGT A G TXLNG Ensembl:ENSG00000086712 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:16786830..16787015 26863196 MeRIP-seq:(Medium) rs1179106031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3930579,Human_RBP_ID_8226480,Human_RBP_ID_8239722,Human_RBP_ID_18468290,Human_RBP_ID_21997242,Human_RBP_ID_26796979 98883 RMVar_ID_98883 Human_SNP_ID_710660822 m1A Human chrX + 16818522 16818522 16818522 CTATGATGTTCCATTGCTTGTAAACATTGATTACATTAGATTTAACCCCTTCTCCATCTTTTTTC CTATGATGTTCCATTGCTTGTAAACATTGATTGCATTAGATTTAACCCCTTCTCCATCTTTTTTC A G TXLNG Ensembl:ENSG00000086712 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:16818519..16818775 26863196 MeRIP-seq:(Medium) rs1343951964 Functional Loss SNV dbSNP153 33..33 33 - - - 98884 RMVar_ID_98884 Human_SNP_ID_710666281 m1A Human chrX - 16845927 16845927 16845927 CTTTTTTTGTTCTTGTAACAGTTTATTCATGGAGGACACACTGCTAAGATTTCAGATTTTAGCTG CTTTTTTTGTTCTTGTAACAGTTTATTCATGGGGGACACACTGCTAAGATTTCAGATTTTAGCTG T C RBBP7 Ensembl:ENSG00000102054 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs780358523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_732590,Human_RBP_ID_1061837,Human_RBP_ID_1713135,Human_RBP_ID_2072555,Human_RBP_ID_7989896,Human_RBP_ID_8716223,Human_RBP_ID_8934297,Human_RBP_ID_16857753,Human_RBP_ID_17325743,Human_RBP_ID_18917865,Human_RBP_ID_24336551,Human_RBP_ID_27792007 Human_Splice_Rec_2188368,Human_Splice_Rec_2188369,Human_Splice_Rec_2188392,Human_Splice_Rec_2188393,Human_Splice_Rec_2188398,Human_Splice_Rec_2188399,Human_Splice_Rec_2188403,Human_Splice_Rec_2188423,Human_Splice_Rec_2188424,Human_Splice_Rec_2188445,Human_Splice_Rec_2188446 RMVar_hsa_circ_22147,RMVar_hsa_circ_9167,RMVar_hsa_circ_62889,RMVar_hsa_circ_359994 98885 RMVar_ID_98885 Human_SNP_ID_710668592 m1A Human chrX + 16857544 16857544 16857544 CATCTATATAGTACTCCTTCAGCACAGCTGTGACACGTCAGCTCTCACTATATGAACAAATTACA CATCTATATAGTACTCCTTCAGCACAGCTGTGGCACGTCAGCTCTCACTATATGAACAAATTACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:16857543..16857756 26863196 MeRIP-seq:(Medium) rs112423364 Functional Loss SNV dbSNP153 33..33 33 - - - 98886 RMVar_ID_98886 Human_SNP_ID_710668803 m1A Human chrX - 16858734 16858734 16858734 TACATGCCGCAGAATCCTCACATCATTGCTACAAAAACACCATCTTCTGATGTGTTGGTTTTTGA TACATGCCGCAGAATCCTCACATCATTGCTACGAAAACACCATCTTCTGATGTGTTGGTTTTTGA T C RBBP7 Ensembl:ENSG00000102054 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs747840522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93506,Human_RBP_ID_732619,Human_RBP_ID_1061846,Human_RBP_ID_1713194,Human_RBP_ID_2072591,Human_RBP_ID_3249236,Human_RBP_ID_3919732,Human_RBP_ID_8934308,Human_RBP_ID_9264977,Human_RBP_ID_9316399,Human_RBP_ID_17325752,Human_RBP_ID_17440969,Human_RBP_ID_17553787,Human_RBP_ID_18148573,Human_RBP_ID_18454204,Human_RBP_ID_22841143,Human_RBP_ID_26835328,Human_RBP_ID_27146709,Human_RBP_ID_27571067,Human_RBP_ID_27792026 Human_Splice_Rec_2188379,Human_Splice_Rec_2188411,Human_Splice_Rec_2188431,Human_Splice_Rec_2188432,Human_Splice_Rec_2188467,Human_Splice_Rec_2188476 Human_miRNA_ID_2213347 RMVar_hsa_circ_19084,RMVar_hsa_circ_22147,RMVar_hsa_circ_359994,RMVar_hsa_circ_324132,RMVar_hsa_circ_366930,RMVar_hsa_circ_261482,RMVar_hsa_circ_49587,RMVar_hsa_circ_9003,RMVar_hsa_circ_66127,RMVar_hsa_circ_10463,RMVar_hsa_circ_40348,RMVar_hsa_circ_284041,RMVar_hsa_circ_97536,RMVar_hsa_circ_261485,RMVar_hsa_circ_261486 98887 RMVar_ID_98887 Human_SNP_ID_710671410 m1A Human chrX + 16870113 16870113 16870113 GCCGCCTCGGACTCCTCTCGTTAGCCAAGAGCAGCCCGACCGCTGGCGCTCCTGCCTTTCCCAAG GCCGCCTCGGACTCCTCTCGTTAGCCAAGAGCCGCCCGACCGCTGGCGCTCCTGCCTTTCCCAAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:16870026..16870275 32194978 MeRIP-seq:(Medium) rs1011137993 Functional Loss SNV dbSNP153 33..33 33 - - - 98888 RMVar_ID_98888 Human_SNP_ID_710671426 m1A Human chrX - 16870183 16870183 16870183 ACGCGGCGTCTGGGGAGCACCCAGGCAGCAAGACGGGGCCCGGGCTTTCGACAGTGGGGAGTGTG ACGCGGCGTCTGGGGAGCACCCAGGCAGCAAGCCGGGGCCCGGGCTTTCGACAGTGGGGAGTGTG T G RBBP7 Ensembl:ENSG00000102054 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:16869980..16870350;chrX:16869978..16870325;chrX:16870026..16870350;chrX:16869979..16870350;chrX:16870007..16870375;chrX:16869987..16870375;chrX:16869993..16870414 26863196 MeRIP-seq:(Medium) rs1009075990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257795,Human_RBP_ID_732635,Human_RBP_ID_3977088,Human_RBP_ID_5059471,Human_RBP_ID_5330663,Human_RBP_ID_7990138,Human_RBP_ID_8939063,Human_RBP_ID_9409070,Human_RBP_ID_24336673,Human_RBP_ID_27146724 98889 RMVar_ID_98889 Human_SNP_ID_710685062 m1A Human chrX - 16946750 16946750 16946750 CCTCAGCTGCCGCCGCCGCCGCCGCCGCCACCACCGCCGCCGCCACCACCACCCCCACGCCCCGC CCTCAGCTGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCACCACCACCCCCACGCCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chrX:16946701..16946905;chrX:16946701..16946800;chrX:16946696..16946959 26863196 MeRIP-seq:(Medium) rs867580747 Functional Loss SNV dbSNP153 33..33 33 - - - 98890 RMVar_ID_98890 Human_SNP_ID_710685063 m1A Human chrX - 16946750 16946750 16946750 CCTCAGCTGCCGCCGCCGCCGCCGCCGCCACCACCGCCGCCGCCACCACCACCCCCACGCCCCGC CCTCAGCTGCCGCCGCCGCCGCCGCCGCCACCCCCGCCGCCGCCACCACCACCCCCACGCCCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chrX:16946701..16946905;chrX:16946701..16946800;chrX:16946696..16946959 26863196 MeRIP-seq:(Medium) rs867580747 Functional Loss SNV dbSNP153 33..33 33 - - - 98891 RMVar_ID_98891 Human_SNP_ID_710685101 m1A Human chrX + 16946775 16946775 16946775 GCGGCGGTGGTGGCGGCGGCGGCGGCGGCGGCAGCTGAGGCCGAGGAGGCGGTGGCTGTGGCGGA GCGGCGGTGGTGGCGGCGGCGGCGGCGGCGGCGGCTGAGGCCGAGGAGGCGGTGGCTGTGGCGGA A G REPS2 Ensembl:ENSG00000169891 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chrX:16946663..16946853;chrX:16946726..16946843 26863196 MeRIP-seq:(Medium) rs867051441 Functional Loss SNV dbSNP153 33..33 33 - - - 98892 RMVar_ID_98892 Human_SNP_ID_710785800 m1A Human chrX + 17567737 17567736 17567738 AAAAGAAAAAGAGAGGAGGGAGAAGGAGAAGAAGAGAGAGAAAGAGAGAAGGAGAGAGGGAAACA AAAAGAAAAAGAGAGGAGGGAGAAGGAGAAGA__AGAGAGAAAGAGAGAAGGAGAGAGGGAAACA AAG A NHS,Z93022.1 Ensembl:ENSG00000188158,Ensembl:ENSG00000235834 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17567642..17567858 26863196 MeRIP-seq:(Medium) rs1401583043 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26267380 98893 RMVar_ID_98893 Human_SNP_ID_710785801 m1A Human chrX + 17567746 17567742 17567746 AGAGAGGAGGGAGAAGGAGAAGAAGAGAGAGAAAGAGAGAAGGAGAGAGGGAAACAGGCAAGAAA AGAGAGGAGGGAGAAGGAGAAGAAGAGAG____AGAGAGAAGGAGAGAGGGAAACAGGCAAGAAA GAGAA G NHS,Z93022.1 Ensembl:ENSG00000188158,Ensembl:ENSG00000235834 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:17567623..17567880 26863196 MeRIP-seq:(Medium) rs989138531 Functional Loss DEL dbSNP153 30..33 33 - - - 98894 RMVar_ID_98894 Human_SNP_ID_710785802 m1A Human chrX + 17567746 17567746 17567746 AGAGAGGAGGGAGAAGGAGAAGAAGAGAGAGAAAGAGAGAAGGAGAGAGGGAAACAGGCAAGAAA AGAGAGGAGGGAGAAGGAGAAGAAGAGAGAGACAGAGAGAAGGAGAGAGGGAAACAGGCAAGAAA A C NHS,Z93022.1 Ensembl:ENSG00000188158,Ensembl:ENSG00000235834 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:17567623..17567880 26863196 MeRIP-seq:(Medium) rs1471048932 Functional Loss SNV dbSNP153 33..33 33 - - - 98895 RMVar_ID_98895 Human_SNP_ID_710792430 m1A Human chrX + 17609762 17609762 17609762 CATGAGAGTTAAGGGGACCATTGATCTATGGCAGTAGCTGAGGTGATGGGAAGTAAGGAGTGGCT CATGAGAGTTAAGGGGACCATTGATCTATGGCTGTAGCTGAGGTGATGGGAAGTAAGGAGTGGCT A T NHS Ensembl:ENSG00000188158 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17609758..17609824 26863196 MeRIP-seq:(Medium) rs1454515675 Functional Loss SNV dbSNP153 33..33 33 - - - 98896 RMVar_ID_98896 Human_SNP_ID_710796086 m1A Human chrX - 17635568 17635568 17635568 CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCATGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCTTGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG T A lnc-RAI2-5,lnc-RAI2-5:2,lnc-RAI2-5:3 RNACentral:URS0000D5B304,RNACentral:URS0000EA6E76,RNACentral:URS0000D5C3F1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17635555..17635631 26863196 MeRIP-seq:(Medium) rs756852916 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13072 98897 RMVar_ID_98897 Human_SNP_ID_710796087 m1A Human chrX - 17635568 17635568 17635568 CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCATGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCGTGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG T C lnc-RAI2-5,lnc-RAI2-5:2,lnc-RAI2-5:3 RNACentral:URS0000D5B304,RNACentral:URS0000EA6E76,RNACentral:URS0000D5C3F1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17635555..17635631 26863196 MeRIP-seq:(Medium) rs756852916 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13072 98898 RMVar_ID_98898 Human_SNP_ID_710796088 m1A Human chrX - 17635568 17635568 17635568 CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCATGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG CTGCATTCTTGGGCATGCAGCAGGCCAGAGCCCTGCTTGGATTCCCGCTCTGCTCCTTAAGGAAG T G lnc-RAI2-5,lnc-RAI2-5:2,lnc-RAI2-5:3 RNACentral:URS0000D5B304,RNACentral:URS0000EA6E76,RNACentral:URS0000D5C3F1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17635555..17635631 26863196 MeRIP-seq:(Medium) rs756852916 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13072 98899 RMVar_ID_98899 Human_SNP_ID_710808113 m1A Human chrX + 17718898 17718896 17718899 AGGAAAGAAGGAAGGAGGAAGTAAGGAAGGAAAGAAGGAAGAGGAAAGGAAGGAAGAAAGGAAGG AGGAAAGAAGGAAGGAGGAAGTAAGGAAGGA___AAGGAAGAGGAAAGGAAGGAAGAAAGGAAGG AAAG A NHS Ensembl:ENSG00000188158 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:17718368..17719182 26863196 MeRIP-seq:(Medium) rs1370512203 Functional Loss DEL dbSNP153 32..34 33 - - - 98900 RMVar_ID_98900 Human_SNP_ID_710811648 m1A Human chrX - 17738322 17738322 17738322 GAGGAGGGAGGGACGCGATCCGCCACCAACCAAATCAGGGCCTTTCCTGTTAACGACCACGCGGC GAGGAGGGAGGGACGCGATCCGCCACCAACCAGATCAGGGCCTTTCCTGTTAACGACCACGCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:17738274..17738356 26863196 MeRIP-seq:(Medium) rs916288922 Functional Loss SNV dbSNP153 33..33 33 - - - 98901 RMVar_ID_98901 Human_SNP_ID_710971835 m1A Human chrX - 18674924 18674924 18674924 GTCTGCTTTACACGCAGAAGGTCCTGGGTTCGAGCCCCAGTGGAACCATAGCCGTAAGGCGGCTG GTCTGCTTTACACGCAGAAGGTCCTGGGTTCGGGCCCCAGTGGAACCATAGCCGTAAGGCGGCTG T C tRNA-Val-TAC-1-1 RNACentral:URS000070B37B tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1298175795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_732815,Human_RBP_ID_1713376,Human_RBP_ID_2072716,Human_RBP_ID_3920025,Human_RBP_ID_7991115,Human_RBP_ID_8276934,Human_RBP_ID_8716620,Human_RBP_ID_16860072,Human_RBP_ID_18918085,Human_RBP_ID_22841156,Human_RBP_ID_23142439,Human_RBP_ID_24357779,Human_RBP_ID_27152531 98902 RMVar_ID_98902 Human_SNP_ID_711089251 m1A Human chrX - 19343996 19343996 19343996 GCAGTGGCGGCAGCGGCGACTCCTCACAACCCAGGAGGCACGACGCGGGTGCCCCCAAGTCTCCT GCAGTGGCGGCAGCGGCGACTCCTCACAACCCCGGAGGCACGACGCGGGTGCCCCCAAGTCTCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19343926..19344157 26863196 MeRIP-seq:(Medium) rs772091896 Functional Loss SNV dbSNP153 33..33 33 - - - 98903 RMVar_ID_98903 Human_SNP_ID_711091623 m1A Human chrX - 19355736 19355736 19355736 TAGAGCCTTACCTTCCCAGATCTACAATAGGCAGCAGCAAACCTTGTTGCCTCTCGGACGCACAG TAGAGCCTTACCTTCCCAGATCTACAATAGGCCGCAGCAAACCTTGTTGCCTCTCGGACGCACAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:19355688..19355802 26863196 MeRIP-seq:(Medium) rs763733376 Functional Loss SNV dbSNP153 33..33 33 - - - 98904 RMVar_ID_98904 Human_SNP_ID_711092725 m1A Human chrX + 19359652 19359643 19359652 CAATCAGTGGATCAAGTTTAAGTCAGTCAGTTAAGGGGAGGAGAAGGAGAGGTTATACCTTCAGG CAATCAGTGGATCAAGTTTAAGTC_________AGGGGAGGAGAAGGAGAGGTTATACCTTCAGG CAGTCAGTTA C PDHA1 Ensembl:ENSG00000131828 Protein coding stop codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19359602..19359725 26863196 MeRIP-seq:(Medium) rs1304934077 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_94894,Human_RBP_ID_732876,Human_RBP_ID_800541,Human_RBP_ID_3249927,Human_RBP_ID_5059965,Human_RBP_ID_7991295,Human_RBP_ID_17667025,Human_RBP_ID_23216812,Human_RBP_ID_24337269 98905 RMVar_ID_98905 Human_SNP_ID_711139191 m1A Human chrX - 19580764 19580762 19580765 AAGGCCTAGGAGCCATCCAAAAGGGTAGGAGGAGTGTGATGTCATGGAAGCTAGAAGGAGGAAGT AAGGCCTAGGAGCCATCCAAAAGGGTAGGAG___TGTGATGTCATGGAAGCTAGAAGGAGGAAGT ACTC A SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19580763..19580846 26863196 MeRIP-seq:(Medium) rs753423835 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_64731,RMVar_hsa_circ_347186,RMVar_hsa_circ_365976,RMVar_hsa_circ_72129,RMVar_hsa_circ_365741,RMVar_hsa_circ_268547,RMVar_hsa_circ_25566,RMVar_hsa_circ_40577,RMVar_hsa_circ_12498 98906 RMVar_ID_98906 Human_SNP_ID_711141298 m1A Human chrX - 19592131 19592131 19592131 ACCCTTTCCCTCCTAGGCACCACTGAGAGAAAACATGAAATTAAAAAGATACCTCCTGAAAGACC ACCCTTTCCCTCCTAGGCACCACTGAGAGAAAGCATGAAATTAAAAAGATACCTCCTGAAAGACC T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:19592035..19592196 26863196 MeRIP-seq:(Medium) rs372562490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2190233,Human_Splice_Rec_2190234,Human_Splice_Rec_2190256,Human_Splice_Rec_2190257,Human_Splice_Rec_2190288,Human_Splice_Rec_2190289,Human_Splice_Rec_2190321,Human_Splice_Rec_2190322,Human_Splice_Rec_2190359,Human_Splice_Rec_2190360,Human_Splice_Rec_2190369,Human_Splice_Rec_2190370,Human_Splice_Rec_2190383 RMVar_hsa_circ_2002,RMVar_hsa_circ_64731,RMVar_hsa_circ_347186,RMVar_hsa_circ_365976,RMVar_hsa_circ_72129,RMVar_hsa_circ_268547,RMVar_hsa_circ_25566,RMVar_hsa_circ_40577,RMVar_hsa_circ_74504,RMVar_hsa_circ_12498,RMVar_hsa_circ_57579,RMVar_hsa_circ_83738,RMVar_hsa_circ_261624 98907 RMVar_ID_98907 Human_SNP_ID_711143927 m1A Human chrX - 19607872 19607872 19607872 GTGGCTCCCATGTTGGGACTTGGGATGGGGGAAGTTTGGTGTAATGTTGAAGAGCACTGGCATTT GTGGCTCCCATGTTGGGACTTGGGATGGGGGAGGTTTGGTGTAATGTTGAAGAGCACTGGCATTT T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19607869..19607953 26863196 MeRIP-seq:(Medium) rs1286275058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2002,RMVar_hsa_circ_64731,RMVar_hsa_circ_365976,RMVar_hsa_circ_72129,RMVar_hsa_circ_268547,RMVar_hsa_circ_25566,RMVar_hsa_circ_74504,RMVar_hsa_circ_12498,RMVar_hsa_circ_57579,RMVar_hsa_circ_112181,RMVar_hsa_circ_83738,RMVar_hsa_circ_261624,RMVar_hsa_circ_261625 98908 RMVar_ID_98908 Human_SNP_ID_711177032 m1A Human chrX - 19802624 19802624 19802624 AGGGTATAGTGTGAGTGTGAACAGAGGCCTACAGCTTGATGAGTACCTAGAAATAAGCCTTGCCA AGGGTATAGTGTGAGTGTGAACAGAGGCCTACGGCTTGATGAGTACCTAGAAATAAGCCTTGCCA T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19802622..19802736 26863196 MeRIP-seq:(Medium) rs750159210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83738,RMVar_hsa_circ_261624,RMVar_hsa_circ_366222,RMVar_hsa_circ_360809,RMVar_hsa_circ_59312,RMVar_hsa_circ_44711,RMVar_hsa_circ_283375,RMVar_hsa_circ_337027,RMVar_hsa_circ_306502,RMVar_hsa_circ_296730 98909 RMVar_ID_98909 Human_SNP_ID_711178887 m1A Human chrX + 19813956 19813956 19813956 ATGCATGATTTCACATCACAGGGTGACAGGTAAGAAAAGCAGCCATCCTTGCATCAAACAGGAAT ATGCATGATTTCACATCACAGGGTGACAGGTACGAAAAGCAGCCATCCTTGCATCAAACAGGAAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:19813954..19814147 26863196 MeRIP-seq:(Medium) rs901872383 Functional Loss SNV dbSNP153 33..33 33 - - - 98910 RMVar_ID_98910 Human_SNP_ID_711182185 m1A Human chrX - 19833371 19833371 19833371 GGGAAGGAAGGAGGACTGTGGGAAGGGGAGAAAGACCATGGGAAAGAGGTAGGGGGACCCTGGGA GGGAAGGAAGGAGGACTGTGGGAAGGGGAGAAGGACCATGGGAAAGAGGTAGGGGGACCCTGGGA T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:19833362..19833699 26863196 MeRIP-seq:(Medium) rs1345549245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83738,RMVar_hsa_circ_261624,RMVar_hsa_circ_366222,RMVar_hsa_circ_360809,RMVar_hsa_circ_59312,RMVar_hsa_circ_44711,RMVar_hsa_circ_283375,RMVar_hsa_circ_337027,RMVar_hsa_circ_261633,RMVar_hsa_circ_306502,RMVar_hsa_circ_296730 98911 RMVar_ID_98911 Human_SNP_ID_711206144 m1A Human chrX - 19970284 19970284 19970284 TCCTGTGTTTCTTTGCAGTGTAAAAAGTGGATAGTGGCTCACGTGTCAAAGGATGGCACGGTCAC TCCTGTGTTTCTTTGCAGTGTAAAAAGTGGATGGTGGCTCACGTGTCAAAGGATGGCACGGTCAC T C BCLAF3 Ensembl:ENSG00000173681 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:19970237..19970343;chrX:19970235..19970328 26863196 MeRIP-seq:(Medium) rs557627256 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_24337462 Human_Splice_Rec_2190400,Human_Splice_Rec_2190448 RMVar_hsa_circ_291158,RMVar_hsa_circ_261635,RMVar_hsa_circ_271810,RMVar_hsa_circ_261642,RMVar_hsa_circ_274628,RMVar_hsa_circ_261643,RMVar_hsa_circ_271162,RMVar_hsa_circ_261646,RMVar_hsa_circ_328252,RMVar_hsa_circ_261648,RMVar_hsa_circ_291849,RMVar_hsa_circ_261650 98912 RMVar_ID_98912 Human_SNP_ID_711209888 m1A Human chrX - 19991009 19991009 19991009 GGCAGAGGTGGCTGGGGTGTCGCTGCTGTGGGAGGCGGCGGCAGAGTGAGGGGCGAGGCCCGAGG GGCAGAGGTGGCTGGGGTGTCGCTGCTGTGGGGGGCGGCGGCAGAGTGAGGGGCGAGGCCCGAGG T C LOC729609,RF00017-4520 RNACentral:URS00009B745B,RNACentral:URS000099C2D3 lincRNA,SRP RNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chrX:19990864..19991039;chrX:19990876..19991027 26863196 MeRIP-seq:(Medium) rs1255382485 Functional Loss SNV dbSNP153 33..33 33 - - - 98913 RMVar_ID_98913 Human_SNP_ID_711214624 m1A Human chrX - 20016161 20016161 20016161 AAAGGCAGGCGAGGAGGCCAAGCGGAAGGCTGAGGAGGAGCTGTTGTTGAAAGAAAAGCAAGAAC AAAGGCAGGCGAGGAGGCCAAGCGGAAGGCTGGGGAGGAGCTGTTGTTGAAAGAAAAGCAAGAAC T C MAP7D2 Ensembl:ENSG00000184368 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:20016110..20016308 26863196 MeRIP-seq:(Medium) rs1420784181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258163 Human_Splice_Rec_2190505,Human_Splice_Rec_2190536,Human_Splice_Rec_2190564,Human_Splice_Rec_2190592 98914 RMVar_ID_98914 Human_SNP_ID_711216110 m1A Human chrX - 20024898 20024898 20024898 TCGGTGTGATCTCATGTAACTGTTGTGTTGGAAAGAGCAGCTTGCCTTTCTTTTTACAGCGTTGG TCGGTGTGATCTCATGTAACTGTTGTGTTGGACAGAGCAGCTTGCCTTTCTTTTTACAGCGTTGG T G MAP7D2 Ensembl:ENSG00000184368 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:20024895..20024983 26863196 MeRIP-seq:(Medium) rs1171785807 Functional Loss SNV dbSNP153 33..33 33 - - - 98915 RMVar_ID_98915 Human_SNP_ID_711222970 m1A Human chrX - 20063511 20063511 20063511 AAGAGCCAGGCTGCAGTACGAAAAGCAAATGGAGGAGCGATGGCGAAAACTGGAAGAGCAGCGGC AAGAGCCAGGCTGCAGTACGAAAAGCAAATGGGGGAGCGATGGCGAAAACTGGAAGAGCAGCGGC T C MAP7D2 Ensembl:ENSG00000184368 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:20063463..20063593 26863196 MeRIP-seq:(Medium) rs967887245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2190491,Human_Splice_Rec_2190492,Human_Splice_Rec_2190520,Human_Splice_Rec_2190521,Human_Splice_Rec_2190551,Human_Splice_Rec_2190552,Human_Splice_Rec_2190578,Human_Splice_Rec_2190579 RMVar_hsa_circ_5547,RMVar_hsa_circ_25587 98916 RMVar_ID_98916 Human_SNP_ID_711237711 m1A Human chrX + 20141778 20141778 20141778 AGGTGCTGGAGGCCAGGCAACGTGCGCGGGAGAGGCTGGCGACCCAGCTCTTCAGAGATCCGCCT AGGTGCTGGAGGCCAGGCAACGTGCGCGGGAGTGGCTGGCGACCCAGCTCTTCAGAGATCCGCCT A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:20141676..20141844 26863410 MeRIP-seq:(Medium) rs1323180448 Functional Loss SNV dbSNP153 33..33 33 - - - 98917 RMVar_ID_98917 Human_SNP_ID_711237725 m1A Human chrX + 20141801 20141801 20141801 GCGCGGGAGAGGCTGGCGACCCAGCTCTTCAGAGATCCGCCTGCGTCCACGCTCGGCGGCAGCAA GCGCGGGAGAGGCTGGCGACCCAGCTCTTCAGGGATCCGCCTGCGTCCACGCTCGGCGGCAGCAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:20141744..20141875;chrX:20141729..20141850;chrX:20141724..20141850 26863196 MeRIP-seq:(Medium) rs1028652091 Functional Loss SNV dbSNP153 33..33 33 - - - 98918 RMVar_ID_98918 Human_SNP_ID_711237726 m1A Human chrX + 20141801 20141801 20141801 GCGCGGGAGAGGCTGGCGACCCAGCTCTTCAGAGATCCGCCTGCGTCCACGCTCGGCGGCAGCAA GCGCGGGAGAGGCTGGCGACCCAGCTCTTCAGTGATCCGCCTGCGTCCACGCTCGGCGGCAGCAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:20141744..20141875;chrX:20141729..20141850;chrX:20141724..20141850 26863196 MeRIP-seq:(Medium) rs1028652091 Functional Loss SNV dbSNP153 33..33 33 - - - 98919 RMVar_ID_98919 Human_SNP_ID_711258877 m1A Human chrX + 20266750 20266718 20266751 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC A_________________________________CGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAG A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1278113430 Functional Loss DEL dbSNP153 2..34 33 - - - 98920 RMVar_ID_98920 Human_SNP_ID_711258894 m1A Human chrX + 20266750 20266732 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCG__________________GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC GGCGGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs921062160 Functional Loss DEL dbSNP153 16..33 33 - - - 98921 RMVar_ID_98921 Human_SNP_ID_711258897 m1A Human chrX + 20266750 20266735 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCG_______________GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC GGCGGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1302774997 Functional Loss DEL dbSNP153 19..33 33 - - - 98922 RMVar_ID_98922 Human_SNP_ID_711258900 m1A Human chrX + 20266750 20266738 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCG____________GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC GGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1241474947 Functional Loss DEL dbSNP153 22..33 33 - - - 98923 RMVar_ID_98923 Human_SNP_ID_711258906 m1A Human chrX + 20266750 20266741 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCG_________GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC GGCGGCGGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1414764503 Functional Loss DEL dbSNP153 25..33 33 - - - 98924 RMVar_ID_98924 Human_SNP_ID_711258915 m1A Human chrX + 20266750 20266747 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCGGCGGCG___GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC GGCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1215736165 Functional Loss DEL dbSNP153 31..33 33 - - - 98925 RMVar_ID_98925 Human_SNP_ID_711258919 m1A Human chrX + 20266750 20266749 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGC_GCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC CA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs1259290461 Functional Loss DEL dbSNP153 33..33 33 - - - 98926 RMVar_ID_98926 Human_SNP_ID_711258920 m1A Human chrX + 20266750 20266750 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs12396661 Functional Loss SNV dbSNP153 33..33 33 - - - 98927 RMVar_ID_98927 Human_SNP_ID_711529701 m1A Human chrX + 21839694 21839694 21839694 CGCGGTCAGCTGTTGGCGGTGCAGGGAGGAGGACGCCGGGGCTCGCCTTCCCTCCTCTGCCGCCG CGCGGTCAGCTGTTGGCGGTGCAGGGAGGAGGGCGCCGGGGCTCGCCTTCCCTCCTCTGCCGCCG A G MBTPS2 Ensembl:ENSG00000012174 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:21839648..21839775 26863196 MeRIP-seq:(Medium) rs1438119168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257819,Human_RBP_ID_5075763 98928 RMVar_ID_98928 Human_SNP_ID_711554042 m1A Human chrX - 21971879 21971879 21971879 CTCAAATTGGCAAAGCTACAAAGGAAAATATAATTTTAAGCTTAAGAATTGTATCGGGGCATTAA CTCAAATTGGCAAAGCTACAAAGGAAAATATAGTTTTAAGCTTAAGAATTGTATCGGGGCATTAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:21971876..21971925 26863196 MeRIP-seq:(Medium) rs765822661 Functional Loss SNV dbSNP153 33..33 33 - - - 98929 RMVar_ID_98929 Human_SNP_ID_711558794 m1A Human chrX - 21994651 21994645 21994651 CAAATTGAAGATCTACCAAAACAAAAACAAAAACAAAAGCCCACAGAGAAATAAAAAGGAACAAA CAAATTGAAGATCTACCAAAACAAAAACAAAA______GCCCACAGAGAAATAAAAAGGAACAAA CTTTTGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:21994600..21994686 26863196 MeRIP-seq:(Medium) rs368911798 Functional Loss DEL dbSNP153 33..38 33 - - - 98930 RMVar_ID_98930 Human_SNP_ID_711763658 m1A Human chrX + 23075721 23075721 23075721 GCACGGCGGAGAGGCGGGCGGGAGGCCGGAGCATATTAATGAAAAGTGCCATAAACTGAAAAACC GCACGGCGGAGAGGCGGGCGGGAGGCCGGAGCCTATTAATGAAAAGTGCCATAAACTGAAAAACC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:23075641..23075730 26863410 MeRIP-seq:(Medium) rs1158120930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18149144 98931 RMVar_ID_98931 Human_SNP_ID_711763659 m1A Human chrX + 23075721 23075721 23075721 GCACGGCGGAGAGGCGGGCGGGAGGCCGGAGCATATTAATGAAAAGTGCCATAAACTGAAAAACC GCACGGCGGAGAGGCGGGCGGGAGGCCGGAGCTTATTAATGAAAAGTGCCATAAACTGAAAAACC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:23075641..23075730 26863410 MeRIP-seq:(Medium) rs1158120930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18149144 98932 RMVar_ID_98932 Human_SNP_ID_711878989 m1A Human chrX + 23667706 23667706 23667706 TGCAGGGCTGGGAGACAGAGGAGAGGCCCCGGACTCGCGAAGAGGAGTGCCACTTCTACGCGGGT TGCAGGGCTGGGAGACAGAGGAGAGGCCCCGGTCTCGCGAAGAGGAGTGCCACTTCTACGCGGGT A T PRDX4 Ensembl:ENSG00000123131 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:23667501..23667859;chrX:23667505..23667757;chrX:23667501..23667754 26863196 MeRIP-seq:(Medium) rs1442856138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257297,Human_RBP_ID_733357,Human_RBP_ID_799401,Human_RBP_ID_848904,Human_RBP_ID_1713631,Human_RBP_ID_5060453,Human_RBP_ID_7993028,Human_RBP_ID_22467881,Human_RBP_ID_22778075,Human_RBP_ID_24338056 Human_miRNA_ID_2709408 RMVar_hsa_circ_102679,RMVar_hsa_circ_261762 98933 RMVar_ID_98933 Human_SNP_ID_711878990 m1A Human chrX - 23667708 23667708 23667708 CCACCCGCGTAGAAGTGGCACTCCTCTTCGCGAGTCCGGGGCCTCTCCTCTGTCTCCCAGCCCTG CCACCCGCGTAGAAGTGGCACTCCTCTTCGCGCGTCCGGGGCCTCTCCTCTGTCTCCCAGCCCTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:23667526..23671401 26863196 MeRIP-seq:(Medium) rs754707782 Functional Loss SNV dbSNP153 33..33 33 - - - 98934 RMVar_ID_98934 Human_SNP_ID_711893738 m1A Human chrX - 23743145 23743145 23743145 GGTTCTCCATCGCGCGCACGGCAGCCTAGCGCAATGAGGCGGGCAGCACTGCGGTAGGTGGCGGG GGTTCTCCATCGCGCGCACGGCAGCCTAGCGCCATGAGGCGGGCAGCACTGCGGTAGGTGGCGGG T G ACOT9 Ensembl:ENSG00000123130 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:23735990..23743250 26863196 MeRIP-seq:(Medium) rs775962184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076053,Human_RBP_ID_9245619,Human_RBP_ID_19148955,Human_RBP_ID_26835339 Human_Splice_Rec_2192497,Human_Splice_Rec_2192526,Human_Splice_Rec_2192594,Human_Splice_Rec_2192645 98935 RMVar_ID_98935 Human_SNP_ID_711893765 m1A Human chrX - 23743247 23743247 23743247 ACCGCTGTCCGGCTCCCGGGCTGTCCTCAGCAAGGGCGCGGTCTGGTACTCGTGCGTCTTTTATC ACCGCTGTCCGGCTCCCGGGCTGTCCTCAGCAGGGGCGCGGTCTGGTACTCGTGCGTCTTTTATC T C ACOT9 Ensembl:ENSG00000123130 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:23743002..23743275 26863196 MeRIP-seq:(Medium) rs189001196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076053,Human_RBP_ID_18427837 98936 RMVar_ID_98936 Human_SNP_ID_711919176 m1A Human chrX + 23870180 23870176 23870180 ATTCATCATGACTGAACATGCCTTCTGACTTCATTCACATAATGCCTCGTCTCCTCTCCACTGAG ATTCATCATGACTGAACATGCCTTCTGAC____TTCACATAATGCCTCGTCTCCTCTCCACTGAG CTTCA C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:23870178..23870309 26863196 MeRIP-seq:(Medium) rs1207578903 Functional Loss DEL dbSNP153 30..33 33 - - - 98937 RMVar_ID_98937 Human_SNP_ID_711921259 m1A Human chrX + 23880906 23880906 23880906 GTGAGTCCTTTTTTGGTGCTGCATAGACTTTGAAGGTGAGCAAGCTCAGGCTGGCTGGCCCCACG GTGAGTCCTTTTTTGGTGCTGCATAGACTTTGGAGGTGAGCAAGCTCAGGCTGGCTGGCCCCACG A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:23880793..23880997 26863196 MeRIP-seq:(Medium) rs778448830 Functional Loss SNV dbSNP153 33..33 33 - - - 98938 RMVar_ID_98938 Human_SNP_ID_711956270 m1A Human chrX - 24054808 24054808 24054808 CACTGCTTGGACATCTCTCCGCTTGAATCTGCACAGTGCCTGTCGGTAGGCTGAGTGGAAAACAC CACTGCTTGGACATCTCTCCGCTTGAATCTGCGCAGTGCCTGTCGGTAGGCTGAGTGGAAAACAC T C RF00017-4620,RF00017-4525 RNACentral:URS000092122F,RNACentral:URS00009368C0 SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:24054707..24054860 26863410 MeRIP-seq:(Medium) rs778817911 Functional Loss SNV dbSNP153 33..33 33 - - - 98939 RMVar_ID_98939 Human_SNP_ID_711956515 m1A Human chrX + 24055651 24055651 24055651 TTACCAAGTTGACGCCACTTTCACACGAAGTTATCAGCAGACAAGCCACAATTAACATAGGTAAG TTACCAAGTTGACGCCACTTTCACACGAAGTTCTCAGCAGACAAGCCACAATTAACATAGGTAAG A C EIF2S3 Ensembl:ENSG00000130741 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:24055626..24055650 26863196 MeRIP-seq:(Medium) rs763418298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_318045,Human_RBP_ID_968462,Human_RBP_ID_3250841,Human_RBP_ID_3977123,Human_RBP_ID_17326000,Human_RBP_ID_18404586,Human_RBP_ID_27792573 Human_Splice_Rec_2192843,Human_Splice_Rec_2192844,Human_Splice_Rec_2192847,Human_Splice_Rec_2192848,Human_Splice_Rec_2192869,Human_Splice_Rec_2192870 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_122556,RMVar_hsa_circ_126313,RMVar_hsa_circ_261789,RMVar_hsa_circ_261790,RMVar_hsa_circ_115201,RMVar_hsa_circ_261791,RMVar_hsa_circ_261793,RMVar_hsa_circ_66392,RMVar_hsa_circ_261792 98940 RMVar_ID_98940 Human_SNP_ID_711956516 m1A Human chrX + 24055651 24055651 24055651 TTACCAAGTTGACGCCACTTTCACACGAAGTTATCAGCAGACAAGCCACAATTAACATAGGTAAG TTACCAAGTTGACGCCACTTTCACACGAAGTTGTCAGCAGACAAGCCACAATTAACATAGGTAAG A G EIF2S3 Ensembl:ENSG00000130741 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:24055626..24055650 26863196 MeRIP-seq:(Medium) rs763418298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_318045,Human_RBP_ID_968462,Human_RBP_ID_3250841,Human_RBP_ID_3977123,Human_RBP_ID_17326000,Human_RBP_ID_18404586,Human_RBP_ID_27792573 Human_Splice_Rec_2192843,Human_Splice_Rec_2192844,Human_Splice_Rec_2192847,Human_Splice_Rec_2192848,Human_Splice_Rec_2192869,Human_Splice_Rec_2192870 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_122556,RMVar_hsa_circ_126313,RMVar_hsa_circ_261789,RMVar_hsa_circ_261790,RMVar_hsa_circ_115201,RMVar_hsa_circ_261791,RMVar_hsa_circ_261793,RMVar_hsa_circ_66392,RMVar_hsa_circ_261792 98941 RMVar_ID_98941 Human_SNP_ID_711956885 m1A Human chrX + 24057408 24057408 24057408 TGTAATTAAATACACATGAATTAATTTTTTGAACTTTGTCCATAGGTACAATTGGTCATGTAGCT TGTAATTAAATACACATGAATTAATTTTTTGAGCTTTGTCCATAGGTACAATTGGTCATGTAGCT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:24057401..24057425 26863196 MeRIP-seq:(Medium) rs755625866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3250845 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_122556,RMVar_hsa_circ_261789,RMVar_hsa_circ_261790,RMVar_hsa_circ_115201,RMVar_hsa_circ_261793,RMVar_hsa_circ_66392,RMVar_hsa_circ_261792 98942 RMVar_ID_98942 Human_SNP_ID_711960727 m1A Human chrX + 24075965 24075965 24075965 GCCTCAAGCCATCCTCCCACCTCAGCCTCTCAAAGTGTTGGGATTACAGACATGAGCCACCCCGC GCCTCAAGCCATCCTCCCACCTCAGCCTCTCAGAGTGTTGGGATTACAGACATGAGCCACCCCGC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1243798529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18918666,Human_RBP_ID_23100738 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_261790,RMVar_hsa_circ_261793,RMVar_hsa_circ_89700,RMVar_hsa_circ_261794,RMVar_hsa_circ_75626,RMVar_hsa_circ_97397,RMVar_hsa_circ_125420,RMVar_hsa_circ_261801,RMVar_hsa_circ_261804,RMVar_hsa_circ_261806,RMVar_hsa_circ_126309,RMVar_hsa_circ_261808,RMVar_hsa_circ_103930,RMVar_hsa_circ_107676,RMVar_hsa_circ_261809,RMVar_hsa_circ_261810 98943 RMVar_ID_98943 Human_SNP_ID_711960973 m1A Human chrX + 24077168 24077168 24077168 GGCGTGATCTGCAACCTCTGCCCCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC GGCGTGATCTGCAACCTCTGCCCCCCGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1379186500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733657,Human_RBP_ID_7994282,Human_RBP_ID_16866057,Human_RBP_ID_18149455 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_261790,RMVar_hsa_circ_261793,RMVar_hsa_circ_89700,RMVar_hsa_circ_261794,RMVar_hsa_circ_88478,RMVar_hsa_circ_75626,RMVar_hsa_circ_97397,RMVar_hsa_circ_125420,RMVar_hsa_circ_261801,RMVar_hsa_circ_261804,RMVar_hsa_circ_261806,RMVar_hsa_circ_126309,RMVar_hsa_circ_261808,RMVar_hsa_circ_103930,RMVar_hsa_circ_107676,RMVar_hsa_circ_261809,RMVar_hsa_circ_261810,RMVar_hsa_circ_261812 98944 RMVar_ID_98944 Human_SNP_ID_711961016 m1A Human chrX + 24077426 24077426 24077426 GCCACAACCAGCCTTTGCTGTAGCACACACATATATCACTGAACCTGTTTGAAATAAAGTTTTTT GCCACAACCAGCCTTTGCTGTAGCACACACATGTATCACTGAACCTGTTTGAAATAAAGTTTTTT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:24077376..24077425 32194978 MeRIP-seq:(Medium) rs1484857345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733666,Human_RBP_ID_1713975,Human_RBP_ID_2073212,Human_RBP_ID_3251004,Human_RBP_ID_3920782,Human_RBP_ID_7994293,Human_RBP_ID_8717468,Human_RBP_ID_8934740,Human_RBP_ID_16866081,Human_RBP_ID_17326027,Human_RBP_ID_17441217,Human_RBP_ID_17554090,Human_RBP_ID_18404604,Human_RBP_ID_24338395,Human_RBP_ID_26574909,Human_RBP_ID_26743505,Human_RBP_ID_27147047,Human_RBP_ID_27551364,Human_RBP_ID_27792596 Human_Splice_Rec_2192878 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_261790,RMVar_hsa_circ_261793,RMVar_hsa_circ_89700,RMVar_hsa_circ_261794,RMVar_hsa_circ_88478,RMVar_hsa_circ_75626,RMVar_hsa_circ_97397,RMVar_hsa_circ_125420,RMVar_hsa_circ_261801,RMVar_hsa_circ_261804,RMVar_hsa_circ_261806,RMVar_hsa_circ_126309,RMVar_hsa_circ_261808,RMVar_hsa_circ_103930,RMVar_hsa_circ_107676,RMVar_hsa_circ_261809,RMVar_hsa_circ_261810,RMVar_hsa_circ_261812 98945 RMVar_ID_98945 Human_SNP_ID_711961099 m1A Human chrX + 24077922 24077922 24077922 ATTATGATTGTGACATAGATTATACTACTACTAATTTTTGGATGTTTCAAAAGGTCAAGAAGTAA ATTATGATTGTGACATAGATTATACTACTACTCATTTTTGGATGTTTCAAAAGGTCAAGAAGTAA A C EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:24077871..24077971 32194978 MeRIP-seq:(Medium) rs1485867854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733672,Human_RBP_ID_1062186,Human_RBP_ID_1248474,Human_RBP_ID_1713988,Human_RBP_ID_2073223,Human_RBP_ID_3251020,Human_RBP_ID_3920788,Human_RBP_ID_7994318,Human_RBP_ID_8162973,Human_RBP_ID_8227184,Human_RBP_ID_8717478,Human_RBP_ID_8934742,Human_RBP_ID_8952528,Human_RBP_ID_9245727,Human_RBP_ID_16866126,Human_RBP_ID_17059166,Human_RBP_ID_17326031,Human_RBP_ID_17441222,Human_RBP_ID_17554098,Human_RBP_ID_17718146,Human_RBP_ID_18149464,Human_RBP_ID_18404611,Human_RBP_ID_23301622,Human_RBP_ID_24338405,Human_RBP_ID_24444536,Human_RBP_ID_24526544,Human_RBP_ID_26571028,Human_RBP_ID_27792601 Human_miRNA_ID_2732399 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_261790,RMVar_hsa_circ_261793,RMVar_hsa_circ_89700,RMVar_hsa_circ_261794,RMVar_hsa_circ_88478,RMVar_hsa_circ_75626,RMVar_hsa_circ_97397,RMVar_hsa_circ_125420,RMVar_hsa_circ_261801,RMVar_hsa_circ_261804,RMVar_hsa_circ_261806,RMVar_hsa_circ_126309,RMVar_hsa_circ_261808,RMVar_hsa_circ_103930,RMVar_hsa_circ_107676,RMVar_hsa_circ_261809,RMVar_hsa_circ_261810,RMVar_hsa_circ_261812 98946 RMVar_ID_98946 Human_SNP_ID_711961161 m1A Human chrX + 24078223 24078223 24078223 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCTAA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTTGAACTCCTAA A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs770703518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26571041 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_261790,RMVar_hsa_circ_261793,RMVar_hsa_circ_89700,RMVar_hsa_circ_261794,RMVar_hsa_circ_88478,RMVar_hsa_circ_75626,RMVar_hsa_circ_97397,RMVar_hsa_circ_125420,RMVar_hsa_circ_261801,RMVar_hsa_circ_261804,RMVar_hsa_circ_261806,RMVar_hsa_circ_126309,RMVar_hsa_circ_261808,RMVar_hsa_circ_103930,RMVar_hsa_circ_107676,RMVar_hsa_circ_261809,RMVar_hsa_circ_261810,RMVar_hsa_circ_261812 98947 RMVar_ID_98947 Human_SNP_ID_711974020 m1A Human chrX - 24149206 24149206 24149206 TCCTGGCCGAGGCTCCAGCTCGAGTTGTTTGCAGGCCCTCAGACCCCCGCCCGCAGTAAATGTGT TCCTGGCCGAGGCTCCAGCTCGAGTTGTTTGCTGGCCCTCAGACCCCCGCCCGCAGTAAATGTGT T A ZFX-AS1 Ensembl:ENSG00000234230 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:24149156..24149544 26863196 MeRIP-seq:(Medium) rs1224824942 Functional Loss SNV dbSNP153 33..33 33 - - - 98948 RMVar_ID_98948 Human_SNP_ID_711974171 m1A Human chrX - 24149769 24149744 24149770 GACTCACCGGACGGACGTGCGGGCGGCCGGCGACGGTGGCGGGTGCTGCAGGCCGGCCTTTCTCT GACTCACCGGACGGACGTGCGGGCGGCCGGC__________________________CTTTCTCT GGCCGGCCTGCAGCACCCGCCACCGTC G RF00017-4620,RF00017-4490 RNACentral:URS000092122F,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:24149747..24149830 26863196 MeRIP-seq:(Medium) rs1244706376 Functional Loss DEL dbSNP153 32..57 33 - - - 98949 RMVar_ID_98949 Human_SNP_ID_711974335 m1A Human chrX - 24150274 24150261 24150275 TAGCGGAATTTTCTCTCCAGACACCGCCTCCAAGATGGCGGCTCCCCCTCCCGGCAACCCCCTCT TAGCGGAATTTTCTCTCCAGACACCGCCTCC______________CCCTCCCGGCAACCCCCTCT GGGAGCCGCCATCTT G RF00017-4620,RF00017-4490 RNACentral:URS000092122F,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:24150248..24150654 26863196 MeRIP-seq:(Medium) rs1262222767 Functional Loss DEL dbSNP153 32..45 33 - - - 98950 RMVar_ID_98950 Human_SNP_ID_711974606 m1A Human chrX + 24151370 24151370 24151370 CATTGGAGGATCAGGGAGGGACGGGTTCCTGAAGTATTAATAGGTGGCATTTTGAGAAGGTTACC CATTGGAGGATCAGGGAGGGACGGGTTCCTGAGGTATTAATAGGTGGCATTTTGAGAAGGTTACC A G ZFX Ensembl:ENSG00000005889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:24151220..24151579;chrX:24151239..24151524 26863196 MeRIP-seq:(Medium) rs1225819130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16867404 98951 RMVar_ID_98951 Human_SNP_ID_711975252 m1A Human chrX + 24154897 24154897 24154897 CTTAGCAAACTAACGCAGGAACAGAAAACCAAATACCGAATATTCTCACATACAGGTGGGAGCTA CTTAGCAAACTAACGCAGGAACAGAAAACCAATTACCGAATATTCTCACATACAGGTGGGAGCTA A T ZFX Ensembl:ENSG00000005889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:24154889..24155021 26863196 MeRIP-seq:(Medium) rs143325174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101114,RMVar_hsa_circ_118767,RMVar_hsa_circ_373337,RMVar_hsa_circ_261814,RMVar_hsa_circ_261815,RMVar_hsa_circ_375205,RMVar_hsa_circ_337733,RMVar_hsa_circ_261817,RMVar_hsa_circ_63667,RMVar_hsa_circ_261816 98952 RMVar_ID_98952 Human_SNP_ID_711983534 m1A Human chrX + 24199047 24199047 24199047 GCAGCATTAGGCGGTAAGAGGAGGCTCCAGCAAAAGAGTGAGGAGGCATGGTCTTGGTTAGTGAG GCAGCATTAGGCGGTAAGAGGAGGCTCCAGCAGAAGAGTGAGGAGGCATGGTCTTGGTTAGTGAG A G ZFX Ensembl:ENSG00000005889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:24198906..24199192 26863196 MeRIP-seq:(Medium) rs1447019140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118767,RMVar_hsa_circ_261815,RMVar_hsa_circ_63667,RMVar_hsa_circ_72223,RMVar_hsa_circ_121521,RMVar_hsa_circ_261821 98953 RMVar_ID_98953 Human_SNP_ID_712032175 m1A Human chrX - 24465408 24465408 24465408 GCACAGACCCGCCTAGACGCCCGGGTGGCCGCAAGGGCTGGCGCAGCCAAGCCGCACGGATAGGG GCACAGACCCGCCTAGACGCCCGGGTGGCCGCCAGGGCTGGCGCAGCCAAGCCGCACGGATAGGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:24465307..24465474 26863196 MeRIP-seq:(Medium) rs1401956475 Functional Loss SNV dbSNP153 33..33 33 - - - 98954 RMVar_ID_98954 Human_SNP_ID_712041554 m1A Human chrX + 24523496 24523496 24523496 GGTGGCAACTGGTTTGCCGAAGATTGTCCTGGAGGGACTCTGGGGGCAGGGCCAGGTGGTGCAAT GGTGGCAACTGGTTTGCCGAAGATTGTCCTGGGGGGACTCTGGGGGCAGGGCCAGGTGGTGCAAT A G PDK3 Ensembl:ENSG00000067992 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:24523458..24523590 26863196 MeRIP-seq:(Medium) rs980362776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7995376 RMVar_hsa_circ_261824,RMVar_hsa_circ_261823,RMVar_hsa_circ_110310,RMVar_hsa_circ_320785,RMVar_hsa_circ_92326,RMVar_hsa_circ_261825,RMVar_hsa_circ_361124,RMVar_hsa_circ_261828,RMVar_hsa_circ_375610,RMVar_hsa_circ_323453,RMVar_hsa_circ_51841,RMVar_hsa_circ_76668,RMVar_hsa_circ_33623,RMVar_hsa_circ_261830 98955 RMVar_ID_98955 Human_SNP_ID_712080800 m1A Human chrX + 24749409 24749409 24749409 ATAAACATGTATAAGAAATAACAGAAAATATGATAGAAGTAAATGCTCTGTAGATAATTAAAACA ATAAACATGTATAAGAAATAACAGAAAATATGTTAGAAGTAAATGCTCTGTAGATAATTAAAACA A T POLA1 Ensembl:ENSG00000101868 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:24749358..24749521 26863196 MeRIP-seq:(Medium) rs1043854020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10478384,Human_RBP_ID_16871490 RMVar_hsa_circ_46662,RMVar_hsa_circ_2759,RMVar_hsa_circ_4891,RMVar_hsa_circ_69148,RMVar_hsa_circ_335534,RMVar_hsa_circ_348827,RMVar_hsa_circ_75117,RMVar_hsa_circ_98028,RMVar_hsa_circ_105981,RMVar_hsa_circ_361897,RMVar_hsa_circ_89024,RMVar_hsa_circ_261840,RMVar_hsa_circ_261841,RMVar_hsa_circ_123136,RMVar_hsa_circ_261842,RMVar_hsa_circ_60121,RMVar_hsa_circ_42878,RMVar_hsa_circ_119487,RMVar_hsa_circ_261843,RMVar_hsa_circ_261844,RMVar_hsa_circ_48178,RMVar_hsa_circ_89456,RMVar_hsa_circ_261845,RMVar_hsa_circ_60190,RMVar_hsa_circ_59873,RMVar_hsa_circ_40656,RMVar_hsa_circ_23869,RMVar_hsa_circ_351862,RMVar_hsa_circ_32821,RMVar_hsa_circ_23486,RMVar_hsa_circ_50984,RMVar_hsa_circ_375371,RMVar_hsa_circ_261850,RMVar_hsa_circ_268050,RMVar_hsa_circ_68264,RMVar_hsa_circ_112233,RMVar_hsa_circ_261852,RMVar_hsa_circ_311008,RMVar_hsa_circ_261855,RMVar_hsa_circ_106998,RMVar_hsa_circ_29624,RMVar_hsa_circ_369848,RMVar_hsa_circ_335939,RMVar_hsa_circ_261857,RMVar_hsa_circ_339299,RMVar_hsa_circ_301158,RMVar_hsa_circ_331508,RMVar_hsa_circ_261859,RMVar_hsa_circ_261861,RMVar_hsa_circ_261862,RMVar_hsa_circ_261860,RMVar_hsa_circ_347537,RMVar_hsa_circ_70723,RMVar_hsa_circ_331045,RMVar_hsa_circ_50405 98956 RMVar_ID_98956 Human_SNP_ID_712089518 m1A Human chrX - 24802575 24802575 24802575 CCCATCACTCTCTTGGCCTACTTGTCTCTAGCATCACTACCTCCCAAGCCAATCTTCACACTTTG CCCATCACTCTCTTGGCCTACTTGTCTCTAGCCTCACTACCTCCCAAGCCAATCTTCACACTTTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:24802526..24802659 26863196 MeRIP-seq:(Medium) rs1439569082 Functional Loss SNV dbSNP153 33..33 33 - - - 98957 RMVar_ID_98957 Human_SNP_ID_712109740 m1A Human chrX - 24924831 24924830 24924832 CCCACGCCACCCTTATCACCATCCCCTGCTACAGTCAGGAAATGTATCCTTCCTTCCTCCACACC CCCACGCCACCCTTATCACCATCCCCTGCTA__GTCAGGAAATGTATCCTTCCTTCCTCCACACC CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:24924824..24924914 26863196 MeRIP-seq:(Medium) rs899793539 Functional Loss DEL dbSNP153 32..33 33 - - - 98958 RMVar_ID_98958 Human_SNP_ID_712259835 m1A Human chrX - 25815129 25815128 25815129 AGGGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGAGGGAGAGAGAGGGAGAGGGAGGGAGAGGGA AGGGAGGGAGAGGGAGAGAGAGAGAGAGAGAG_GAGGGAGAGAGAGGGAGAGGGAGGGAGAGGGA CT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:25815049..25815162 26863196 MeRIP-seq:(Medium) rs1165810423 Functional Loss DEL dbSNP153 33..33 33 - - - 98959 RMVar_ID_98959 Human_SNP_ID_712259837 m1A Human chrX - 25815129 25815129 25815129 AGGGAGGGAGAGGGAGAGAGAGAGAGAGAGAGAGAGGGAGAGAGAGGGAGAGGGAGGGAGAGGGA AGGGAGGGAGAGGGAGAGAGAGAGAGAGAGAGGGAGGGAGAGAGAGGGAGAGGGAGGGAGAGGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:25815049..25815162 26863196 MeRIP-seq:(Medium) rs1009117696 Functional Loss SNV dbSNP153 33..33 33 - - - 98960 RMVar_ID_98960 Human_SNP_ID_712289284 m1A Human chrX - 25979277 25979272 25979278 CTTGTTAATTTTCTGTCTCGTCGATCTGTCTAATATTGACAGTGGAGTGTTAAAGTCTCCCACTA CTTGTTAATTTTCTGTCTCGTCGATCTGTCT______GACAGTGGAGTGTTAAAGTCTCCCACTA CAATATT C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chrX:25979217..25979301 26863410 MeRIP-seq:(Medium) rs1337233600 Functional Loss DEL dbSNP153 32..37 33 - - - 98961 RMVar_ID_98961 Human_SNP_ID_712613276 m1A Human chrX + 27809471 27809471 27809471 CCCCAACCCCGCCCGCCCCCGCCCCAACCACCACCCCCCCGCCGGCCCCCCCCCCGCCCCGCCCG CCCCAACCCCGCCCGCCCCCGCCCCAACCACCCCCCCCCCGCCGGCCCCCCCCCCGCCCCGCCCG A C MAGEB10 Ensembl:ENSG00000177689 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chrX:27809457..27809554;chrX:27809393..27809624;chrX:27809392..27809627;chrX:27809412..27809607 26863196 MeRIP-seq:(Medium) rs866539575 Functional Loss SNV dbSNP153 33..33 33 - - - 98962 RMVar_ID_98962 Human_SNP_ID_712613306 m1A Human chrX + 27809562 27809545 27809562 GCCGCCGGCCCCCGCCCCGCCCCGCCCCGCCCACCGCCCCCACCCCACCCACCCCCCCTCCTGTC GCCGCCGGCCCCCGCC_________________CCGCCCCCACCCCACCCACCCCCCCTCCTGTC CCCGCCCCGCCCCGCCCA C MAGEB10 Ensembl:ENSG00000177689 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chrX:27809476..27809627;chrX:27809472..27809574 26863196 MeRIP-seq:(Medium) rs1430649647 Functional Loss DEL dbSNP153 17..33 33 - - - 98963 RMVar_ID_98963 Human_SNP_ID_712613315 m1A Human chrX + 27809562 27809562 27809562 GCCGCCGGCCCCCGCCCCGCCCCGCCCCGCCCACCGCCCCCACCCCACCCACCCCCCCTCCTGTC GCCGCCGGCCCCCGCCCCGCCCCGCCCCGCCCCCCGCCCCCACCCCACCCACCCCCCCTCCTGTC A C MAGEB10 Ensembl:ENSG00000177689 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chrX:27809476..27809627;chrX:27809472..27809574 26863196 MeRIP-seq:(Medium) rs1205232174 Functional Loss SNV dbSNP153 33..33 33 - - - 98964 RMVar_ID_98964 Human_SNP_ID_629030180 m1A Human chr17 - 60345610 60345610 60345610 GATTTCTTACCCATCTTCTGTTTCTGAATTGCAGTTACAGATGTAGAGCTAAAACGACTGAAGGA GATTTCTTACCCATCTTCTGTTTCTGAATTGCTGTTACAGATGTAGAGCTAAAACGACTGAAGGA T A USP32 Ensembl:ENSG00000170832 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:60345551..60345723 26863196 MeRIP-seq:(Medium) rs1432848511 Functional Loss SNV dbSNP153 33..33 33 - - - 98965 RMVar_ID_98965 Human_SNP_ID_629041222 m1A Human chr17 - 60391966 60391966 60391966 CGGGAGGGGGGTGGGGGCGAGATCAGGCTCCGACCCCCCGCCGAGGGGATGAGGGGAGCATGGGT CGGGAGGGGGGTGGGGGCGAGATCAGGCTCCGGCCCCCCGCCGAGGGGATGAGGGGAGCATGGGT T C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr17:60391864..60392045;chr17:60391810..60392068 26863196 MeRIP-seq:(Medium) rs758513771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952777,Human_RBP_ID_4466675,Human_RBP_ID_5187505,Human_RBP_ID_5318562,Human_RBP_ID_8092737,Human_RBP_ID_8189772,Human_RBP_ID_8232430,Human_RBP_ID_9422446,Human_RBP_ID_18419687,Human_RBP_ID_22061554,Human_RBP_ID_22959465,Human_RBP_ID_25345396 Human_Splice_Rec_1848733,Human_Splice_Rec_1848917,Human_Splice_Rec_1848925,Human_Splice_Rec_1848953 98966 RMVar_ID_98966 Human_SNP_ID_629041223 m1A Human chr17 - 60391966 60391966 60391966 CGGGAGGGGGGTGGGGGCGAGATCAGGCTCCGACCCCCCGCCGAGGGGATGAGGGGAGCATGGGT CGGGAGGGGGGTGGGGGCGAGATCAGGCTCCGCCCCCCCGCCGAGGGGATGAGGGGAGCATGGGT T G USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr17:60391864..60392045;chr17:60391810..60392068 26863196 MeRIP-seq:(Medium) rs758513771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952777,Human_RBP_ID_4466675,Human_RBP_ID_5187505,Human_RBP_ID_5318562,Human_RBP_ID_8092737,Human_RBP_ID_8189772,Human_RBP_ID_8232430,Human_RBP_ID_9422446,Human_RBP_ID_18419687,Human_RBP_ID_22061554,Human_RBP_ID_22959465,Human_RBP_ID_25345396 Human_Splice_Rec_1848733,Human_Splice_Rec_1848917,Human_Splice_Rec_1848925,Human_Splice_Rec_1848953 98967 RMVar_ID_98967 Human_SNP_ID_629041227 m1A Human chr17 - 60391974 60391974 60391974 GGAGAAGGCGGGAGGGGGGTGGGGGCGAGATCAGGCTCCGACCCCCCGCCGAGGGGATGAGGGGA GGAGAAGGCGGGAGGGGGGTGGGGGCGAGATCGGGCTCCGACCCCCCGCCGAGGGGATGAGGGGA T C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:60345601..60392120 26863410 MeRIP-seq:(Medium) rs755983597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4442932,Human_RBP_ID_5187505,Human_RBP_ID_5318562,Human_RBP_ID_8092737,Human_RBP_ID_8189772,Human_RBP_ID_8232430,Human_RBP_ID_9422446,Human_RBP_ID_18419687,Human_RBP_ID_22061554,Human_RBP_ID_25345396 Human_Splice_Rec_1848733,Human_Splice_Rec_1848917,Human_Splice_Rec_1848925,Human_Splice_Rec_1848953 98968 RMVar_ID_98968 Human_SNP_ID_629041246 m1A Human chr17 - 60392013 60391997 60392013 GGGGACGCCGACACCGTCACCGTCACCCAGGGACGCCGAGGAGAAGGCGGGAGGGGGGTGGGGGC GGGGACGCCGACACCGTCACCGTCACCCAGGG________________GGGAGGGGGGTGGGGGC CGCCTTCTCCTCGGCGT C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:60391610..60392318;chr17:60345551..60392381 26863196 MeRIP-seq:(Medium) rs1173407315 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_4464702,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98969 RMVar_ID_98969 Human_SNP_ID_629041252 m1A Human chr17 - 60392013 60392006 60392013 GGGGACGCCGACACCGTCACCGTCACCCAGGGACGCCGAGGAGAAGGCGGGAGGGGGGTGGGGGC GGGGACGCCGACACCGTCACCGTCACCCAGGG_______GGAGAAGGCGGGAGGGGGGTGGGGGC CTCGGCGT C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:60391610..60392318;chr17:60345551..60392381 26863196 MeRIP-seq:(Medium) rs1275179159 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_4464702,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98970 RMVar_ID_98970 Human_SNP_ID_629041255 m1A Human chr17 - 60392013 60392008 60392013 GGGGACGCCGACACCGTCACCGTCACCCAGGGACGCCGAGGAGAAGGCGGGAGGGGGGTGGGGGC GGGGACGCCGACACCGTCACCGTCACCCAGGG_____GAGGAGAAGGCGGGAGGGGGGTGGGGGC CGGCGT C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:60391610..60392318;chr17:60345551..60392381 26863196 MeRIP-seq:(Medium) rs1217665259 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_4464702,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98971 RMVar_ID_98971 Human_SNP_ID_629041262 m1A Human chr17 - 60392027 60392027 60392027 GGGAGGTGGGGGCGGGGGACGCCGACACCGTCACCGTCACCCAGGGACGCCGAGGAGAAGGCGGG GGGAGGTGGGGGCGGGGGACGCCGACACCGTCGCCGTCACCCAGGGACGCCGAGGAGAAGGCGGG T C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:60391876..60392111 26863196 MeRIP-seq:(Medium) rs570034076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767379,Human_RBP_ID_4442934,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98972 RMVar_ID_98972 Human_SNP_ID_629041263 m1A Human chr17 + 60392029 60392029 60392029 CGCCTTCTCCTCGGCGTCCCTGGGTGACGGTGACGGTGTCGGCGTCCCCCGCCCCCACCTCCCCC CGCCTTCTCCTCGGCGTCCCTGGGTGACGGTGTCGGTGTCGGCGTCCCCCGCCCCCACCTCCCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:60345526..60392154 26863196 MeRIP-seq:(Medium) rs1288260658 Functional Loss SNV dbSNP153 33..33 33 - - - 98973 RMVar_ID_98973 Human_SNP_ID_629041265 m1A Human chr17 - 60392035 60392035 60392035 AGTGTGGGGGGAGGTGGGGGCGGGGGACGCCGACACCGTCACCGTCACCCAGGGACGCCGAGGAG AGTGTGGGGGGAGGTGGGGGCGGGGGACGCCGGCACCGTCACCGTCACCCAGGGACGCCGAGGAG T C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:60391888..60392107 26863410 MeRIP-seq:(Medium) rs535873857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767379,Human_RBP_ID_4442934,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98974 RMVar_ID_98974 Human_SNP_ID_629041266 m1A Human chr17 - 60392041 60392041 60392041 CTTGTTAGTGTGGGGGGAGGTGGGGGCGGGGGACGCCGACACCGTCACCGTCACCCAGGGACGCC CTTGTTAGTGTGGGGGGAGGTGGGGGCGGGGGGCGCCGACACCGTCACCGTCACCCAGGGACGCC T C USP32 Ensembl:ENSG00000170832 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:60391944..60392109 26863410 MeRIP-seq:(Medium) rs916278632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50861,Human_RBP_ID_767379,Human_RBP_ID_4464702,Human_RBP_ID_5318563,Human_RBP_ID_9422447,Human_RBP_ID_18419688 98975 RMVar_ID_98975 Human_SNP_ID_629075480 m1A Human chr17 - 60526007 60526007 60526007 TGCCACCGCCCCTCCGAATCCTCCGGGGCCGCAGAGGGGTTCGCTACGGAGGGAGGTGGGGGCCT TGCCACCGCCCCTCCGAATCCTCCGGGGCCGCTGAGGGGTTCGCTACGGAGGGAGGTGGGGGCCT T A APPBP2 Ensembl:ENSG00000062725 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:60525966..60526173;chr17:60525961..60526206 26863196 MeRIP-seq:(Medium) rs1386487017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444834 98976 RMVar_ID_98976 Human_SNP_ID_629075481 m1A Human chr17 - 60526007 60526007 60526007 TGCCACCGCCCCTCCGAATCCTCCGGGGCCGCAGAGGGGTTCGCTACGGAGGGAGGTGGGGGCCT TGCCACCGCCCCTCCGAATCCTCCGGGGCCGCGGAGGGGTTCGCTACGGAGGGAGGTGGGGGCCT T C APPBP2 Ensembl:ENSG00000062725 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:60525966..60526173;chr17:60525961..60526206 26863196 MeRIP-seq:(Medium) rs1386487017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444834 98977 RMVar_ID_98977 Human_SNP_ID_629093561 m1A Human chr17 + 60600415 60600415 60600415 CGTGGGACCGGCGGGATCCCGGCCAGCCGGCCATGGCGGGGCTGTACTCGCTGGGAGTGAGCGTC CGTGGGACCGGCGGGATCCCGGCCAGCCGGCCTTGGCGGGGCTGTACTCGCTGGGAGTGAGCGTC A T PPM1D Ensembl:ENSG00000170836 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:60600370..60600488 26863196 MeRIP-seq:(Medium) rs1016408106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238115,Human_RBP_ID_4464703 98978 RMVar_ID_98978 Human_SNP_ID_629113765 m1A Human chr17 - 60677969 60677969 60677969 CTGCCAGCCCGACCCAGTCCCCTCACGCCGCCAGTCCCTCGTCCTCCCCAAGCCTCCCCAAAGCC CTGCCAGCCCGACCCAGTCCCCTCACGCCGCCGGTCCCTCGTCCTCCCCAAGCCTCCCCAAAGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:60677918..60678139 26863196 MeRIP-seq:(Medium) rs944362249 Functional Loss SNV dbSNP153 33..33 33 - - - 98979 RMVar_ID_98979 Human_SNP_ID_629222265 m1A Human chr17 - 61142614 61142614 61142614 ATCATTCTATATGACTGCCTCTTCCTGCCTTCACCTCTATATCCCCAAATCCATTTTTTCTGATG ATCATTCTATATGACTGCCTCTTCCTGCCTTCCCCTCTATATCCCCAAATCCATTTTTTCTGATG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:61142607..61142744 26863196 MeRIP-seq:(Medium) rs1013416697 Functional Loss SNV dbSNP153 33..33 33 - - - 98980 RMVar_ID_98980 Human_SNP_ID_629262006 m1A Human chr17 - 61317512 61317509 61317512 TCAATGAAGCCCTCCATGTTGCCATGAGCTGCATTTTCCTGGTCCAGGCCCCAAACACCAGGAAC TCAATGAAGCCCTCCATGTTGCCATGAGCTGC___TTCCTGGTCCAGGCCCCAAACACCAGGAAC AAAT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:61317504..61317657 26863196 MeRIP-seq:(Medium) rs1258614518 Functional Loss DEL dbSNP153 33..35 33 - - - 98981 RMVar_ID_98981 Human_SNP_ID_629284662 m1A Human chr17 + 61405331 61405331 61405331 CAGCGCCAGCCCCACTCGCTTGACCGAACCCGAGCGCGCCCGGGAGCGGCGTAGTCCCGAGAGGG CAGCGCCAGCCCCACTCGCTTGACCGAACCCGGGCGCGCCCGGGAGCGGCGTAGTCCCGAGAGGG A G TBX2 Ensembl:ENSG00000121068 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:61405280..61405929 32194978 MeRIP-seq:(Medium) rs1239861226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94758,RMVar_hsa_circ_186029 98982 RMVar_ID_98982 Human_SNP_ID_629284696 m1A Human chr17 + 61405391 61405391 61405391 GAGGGGCAAGGAGCCGGCCGAGAGCGGCGGGGACGGCCCGTTCGGCCTGAGGAGCCTGGAGAAGG GAGGGGCAAGGAGCCGGCCGAGAGCGGCGGGGGCGGCCCGTTCGGCCTGAGGAGCCTGGAGAAGG A G TBX2 Ensembl:ENSG00000121068 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:61405341..61405417 26863196 MeRIP-seq:(Medium) rs1195162033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22959880 RMVar_hsa_circ_94758,RMVar_hsa_circ_186029 98983 RMVar_ID_98983 Human_SNP_ID_629390144 m1A Human chr17 - 61863451 61863451 61863451 TCGAGGAAAGGTAACGGCGGCCCCAGTCCTGCACACAAGGCCGGGGAAGTAGCAGCACCCCCAGG TCGAGGAAAGGTAACGGCGGCCCCAGTCCTGCGCACAAGGCCGGGGAAGTAGCAGCACCCCCAGG T C BRIP1 Ensembl:ENSG00000136492 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:61863400..61863495;chr17:61863402..61863522 26863196 MeRIP-seq:(Medium) rs1027762321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419692,Human_RBP_ID_26968163,Human_RBP_ID_27838502 RMVar_hsa_circ_81566,RMVar_hsa_circ_186038,RMVar_hsa_circ_186058,RMVar_hsa_circ_79559 98984 RMVar_ID_98984 Human_SNP_ID_629390774 m1A Human chr17 - 61866171 61866171 61866171 TAGTAAAGACGGGGGTTTGCCATGTTGCCCAGACTGGTTTTGAACTCCTGGCCTCAGGTGATCTG TAGTAAAGACGGGGGTTTGCCATGTTGCCCAGTCTGGTTTTGAACTCCTGGCCTCAGGTGATCTG T A INTS2 Ensembl:ENSG00000108506 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7215076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496380 Human_miRNA_ID_2994964 RMVar_hsa_circ_186059,RMVar_hsa_circ_99041,RMVar_hsa_circ_105095,RMVar_hsa_circ_106952,RMVar_hsa_circ_186060,RMVar_hsa_circ_186061 98985 RMVar_ID_98985 Human_SNP_ID_629390775 m1A Human chr17 - 61866171 61866171 61866171 TAGTAAAGACGGGGGTTTGCCATGTTGCCCAGACTGGTTTTGAACTCCTGGCCTCAGGTGATCTG TAGTAAAGACGGGGGTTTGCCATGTTGCCCAGGCTGGTTTTGAACTCCTGGCCTCAGGTGATCTG T C INTS2 Ensembl:ENSG00000108506 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7215076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496380 Human_miRNA_ID_2994964 RMVar_hsa_circ_186059,RMVar_hsa_circ_99041,RMVar_hsa_circ_105095,RMVar_hsa_circ_106952,RMVar_hsa_circ_186060,RMVar_hsa_circ_186061 98986 RMVar_ID_98986 Human_SNP_ID_629406693 m1A Human chr17 - 61927889 61927889 61927889 GTTGAAAAAGTCTCCCGCTTTTCCGTTCCTACAGTCCCGGTTCTGCCTTTGTGTGGTGCCCCCAT GTTGAAAAAGTCTCCCGCTTTTCCGTTCCTACTGTCCCGGTTCTGCCTTTGTGTGGTGCCCCCAT T A INTS2 Ensembl:ENSG00000108506 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:61927840..61927923 26863196 MeRIP-seq:(Medium) rs1382949461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4443505 RMVar_hsa_circ_95873,RMVar_hsa_circ_186095 98987 RMVar_ID_98987 Human_SNP_ID_629422013 m1A Human chr17 + 61982949 61982947 61982950 CTAGCAGGTCCACCAGCTCCACGAGGAGTCCGAGGAGTCCTTGGAGTCCTTGGAGTTGGAAACCG CTAGCAGGTCCACCAGCTCCACGAGGAGTCC___GAGTCCTTGGAGTCCTTGGAGTTGGAAACCG CGAG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:61982898..61982985 32194978 MeRIP-seq:(Medium) rs1225516728 Functional Loss DEL dbSNP153 32..34 33 - - - 98988 RMVar_ID_98988 Human_SNP_ID_629422018 m1A Human chr17 + 61982949 61982949 61982949 CTAGCAGGTCCACCAGCTCCACGAGGAGTCCGAGGAGTCCTTGGAGTCCTTGGAGTTGGAAACCG CTAGCAGGTCCACCAGCTCCACGAGGAGTCCGTGGAGTCCTTGGAGTCCTTGGAGTTGGAAACCG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:61982898..61982985 32194978 MeRIP-seq:(Medium) rs1567958285 Functional Loss SNV dbSNP153 33..33 33 - - - 98989 RMVar_ID_98989 Human_SNP_ID_629446012 m1A Human chr17 + 62065368 62065365 62065368 AGGAGGCCGCCGGGCGCCCGCCCTCCCCACCCACCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG AGGAGGCCGCCGGGCGCCCGCCCTCCCCAC___CCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG CCCA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:62065269..62065425 26863196 MeRIP-seq:(Medium) rs1466061191 Functional Loss DEL dbSNP153 31..33 33 - - - 98990 RMVar_ID_98990 Human_SNP_ID_629446013 m1A Human chr17 + 62065368 62065367 62065368 AGGAGGCCGCCGGGCGCCCGCCCTCCCCACCCACCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG AGGAGGCCGCCGGGCGCCCGCCCTCCCCACCC_CCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG CA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:62065269..62065425 26863196 MeRIP-seq:(Medium) rs1269340422 Functional Loss DEL dbSNP153 33..33 33 - - - 98991 RMVar_ID_98991 Human_SNP_ID_629446014 m1A Human chr17 + 62065368 62065368 62065368 AGGAGGCCGCCGGGCGCCCGCCCTCCCCACCCACCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG AGGAGGCCGCCGGGCGCCCGCCCTCCCCACCCCCCCCCCCGCCGCCGCCGCCGCCGCCGCCGCCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:62065269..62065425 26863196 MeRIP-seq:(Medium) rs573268151 Functional Loss SNV dbSNP153 33..33 33 - - - 98992 RMVar_ID_98992 Human_SNP_ID_629446164 m1A Human chr17 + 62065810 62065810 62065810 CTCTGGCTCTGTCTTCGTGTCGTTCCTGGGCCAAGCCGGCCTAAAGTTTGCCCTCCTGTGGCCTC CTCTGGCTCTGTCTTCGTGTCGTTCCTGGGCCGAGCCGGCCTAAAGTTTGCCCTCCTGTGGCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62065759..62065942 26863196 MeRIP-seq:(Medium) rs114187079 Functional Loss SNV dbSNP153 33..33 33 - - - 98993 RMVar_ID_98993 Human_SNP_ID_629533653 m1A Human chr17 + 62423980 62423980 62423980 AAGAGGCAGCAGTTCGGAAGCCGGTTCCTGAGAGATCCGGCGCGCGTCTTCCACCACAATGCCTG AAGAGGCAGCAGTTCGGAAGCCGGTTCCTGAGCGATCCGGCGCGCGTCTTCCACCACAATGCCTG A C METTL2A Ensembl:ENSG00000087995 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62423942..62424080 26863196 MeRIP-seq:(Medium) rs1053113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465600 Human_Splice_Rec_1850479,Human_Splice_Rec_1850493 98994 RMVar_ID_98994 Human_SNP_ID_629533692 m1A Human chr17 + 62424048 62424048 62424048 ATCACTCTGCCCCTTCGCCCGGCCTGTCGCTGACCCTCTGTCCCGCCGCCTCGGAGCACTCCGAA ATCACTCTGCCCCTTCGCCCGGCCTGTCGCTGGCCCTCTGTCCCGCCGCCTCGGAGCACTCCGAA A G METTL2A Ensembl:ENSG00000087995 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11543000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19083460 GWAS_ID_13073,GWAS_ID_13074 98995 RMVar_ID_98995 Human_SNP_ID_629547521 m1A Human chr17 - 62478953 62478952 62478953 CAAGGGAGGCGCAGGAGGGCCCAGGCCGGGCCAGGAGGTGGGGGCCCGCTCGGCTGGGGGCCACT CAAGGGAGGCGCAGGAGGGCCCAGGCCGGGCC_GGAGGTGGGGGCCCGCTCGGCTGGGGGCCACT CT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:62478851..62479085 26863410 MeRIP-seq:(Medium) rs1396046075 Functional Loss DEL dbSNP153 33..33 33 - - - 98996 RMVar_ID_98996 Human_SNP_ID_629547814 m1A Human chr17 - 62479732 62479732 62479732 AACTCATGTTAAGGAAATAGCCACTCCGTCTAATTCCAGCGGGGCCTTGGACTGGGATCCTCCCT AACTCATGTTAAGGAAATAGCCACTCCGTCTACTTCCAGCGGGGCCTTGGACTGGGATCCTCCCT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:62479730..62479830 32194978 MeRIP-seq:(Medium) rs1181715540 Functional Loss SNV dbSNP153 33..33 33 - - - 98997 RMVar_ID_98997 Human_SNP_ID_629578100 m1A Human chr17 + 62606142 62606142 62606142 ATATTTCTTTTTTGTCCCAGGTATTTACCACCAGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA ATATTTCTTTTTTGTCCCAGGTATTTACCACCGGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA A G TLK2 Ensembl:ENSG00000146872 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8078132 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9346369,Human_RBP_ID_22586633,Human_RBP_ID_22656637 Human_Splice_Rec_1850550,Human_Splice_Rec_1850551,Human_Splice_Rec_1850642,Human_Splice_Rec_1850643,Human_Splice_Rec_1850686,Human_Splice_Rec_1850687,Human_Splice_Rec_1850726,Human_Splice_Rec_1850727,Human_Splice_Rec_1850774,Human_Splice_Rec_1850796,Human_Splice_Rec_1850797 GWAS_ID_13075,GWAS_ID_13076,GWAS_ID_13077 RMVar_hsa_circ_1739,RMVar_hsa_circ_105826,RMVar_hsa_circ_186202,RMVar_hsa_circ_23423,RMVar_hsa_circ_108797,RMVar_hsa_circ_186219,RMVar_hsa_circ_186227,RMVar_hsa_circ_108597,RMVar_hsa_circ_186224,RMVar_hsa_circ_316047,RMVar_hsa_circ_325245,RMVar_hsa_circ_186228,RMVar_hsa_circ_342126 98998 RMVar_ID_98998 Human_SNP_ID_629578101 m1A Human chr17 + 62606142 62606142 62606142 ATATTTCTTTTTTGTCCCAGGTATTTACCACCAGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA ATATTTCTTTTTTGTCCCAGGTATTTACCACCTGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA A T TLK2 Ensembl:ENSG00000146872 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8078132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9346369,Human_RBP_ID_22586633,Human_RBP_ID_22656637 Human_Splice_Rec_1850550,Human_Splice_Rec_1850551,Human_Splice_Rec_1850642,Human_Splice_Rec_1850643,Human_Splice_Rec_1850686,Human_Splice_Rec_1850687,Human_Splice_Rec_1850726,Human_Splice_Rec_1850727,Human_Splice_Rec_1850774,Human_Splice_Rec_1850796,Human_Splice_Rec_1850797 GWAS_ID_13075,GWAS_ID_13076,GWAS_ID_13077 RMVar_hsa_circ_1739,RMVar_hsa_circ_105826,RMVar_hsa_circ_186202,RMVar_hsa_circ_23423,RMVar_hsa_circ_108797,RMVar_hsa_circ_186219,RMVar_hsa_circ_186227,RMVar_hsa_circ_108597,RMVar_hsa_circ_186224,RMVar_hsa_circ_316047,RMVar_hsa_circ_325245,RMVar_hsa_circ_186228,RMVar_hsa_circ_342126 98999 RMVar_ID_98999 Human_SNP_ID_629580740 m1A Human chr17 - 62617356 62617356 62617356 CAGCCTCTGGCAGGTTCCCCCTACCCAACCACAGAACTCAACAGCAACCTGAGTCTCTAGCCACT CAGCCTCTGGCAGGTTCCCCCTACCCAACCACGGAACTCAACAGCAACCTGAGTCTCTAGCCACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62617305..62617398 26863196 MeRIP-seq:(Medium) rs968771163 Functional Loss SNV dbSNP153 33..33 33 - - - 99000 RMVar_ID_99000 Human_SNP_ID_629583038 m1A Human chr17 + 62626866 62626864 62626867 TGAAATTTCCAGCTGGTCTTTTGCTACCGGCCAGCAGTCCAGTTGGTGGGAGTGATGATGCCGGT TGAAATTTCCAGCTGGTCTTTTGCTACCGGC___CAGTCCAGTTGGTGGGAGTGATGATGCCGGT CCAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:62626676..62626869 32194978 MeRIP-seq:(Medium) rs1219164444 Functional Loss DEL dbSNP153 32..34 33 - - - 99001 RMVar_ID_99001 Human_SNP_ID_629583335 m1A Human chr17 - 62627733 62627733 62627733 GCGCACAGGCGCAACGCGCTGTGGCAGCCCCGAGGCTGGGCTGTGATGACCGCCCGCAAGGGGCT GCGCACAGGCGCAACGCGCTGTGGCAGCCCCGTGGCTGGGCTGTGATGACCGCCCGCAAGGGGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:62627109..62664974;chr17:62627426..62627925;chr17:62627101..62628025;chr17:62627202..62628050;chr17:62627429..62628014 26863196 MeRIP-seq:(Medium) rs544970108 Functional Loss SNV dbSNP153 33..33 33 - - - 99002 RMVar_ID_99002 Human_SNP_ID_629583336 m1A Human chr17 - 62627733 62627733 62627733 GCGCACAGGCGCAACGCGCTGTGGCAGCCCCGAGGCTGGGCTGTGATGACCGCCCGCAAGGGGCT GCGCACAGGCGCAACGCGCTGTGGCAGCCCCGGGGCTGGGCTGTGATGACCGCCCGCAAGGGGCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:62627109..62664974;chr17:62627426..62627925;chr17:62627101..62628025;chr17:62627202..62628050;chr17:62627429..62628014 26863196 MeRIP-seq:(Medium) rs544970108 Functional Loss SNV dbSNP153 33..33 33 - - - 99003 RMVar_ID_99003 Human_SNP_ID_629583403 m1A Human chr17 - 62627901 62627900 62627901 GGCAGCGCCTTACCCGGGAGGGCGGCGTCCCCAGGGGCGCCGGGACGGCCGAGGTGCAGGCACCC GGCAGCGCCTTACCCGGGAGGGCGGCGTCCCC_GGGGCGCCGGGACGGCCGAGGTGCAGGCACCC CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:62627451..62627973 26863196 MeRIP-seq:(Medium) rs1323522864 Functional Loss DEL dbSNP153 33..33 33 - - - 99004 RMVar_ID_99004 Human_SNP_ID_629584062 m1A Human chr17 - 62630398 62630398 62630398 TCCAATCTCCAGACGGGAAGCATCCACACTCCAGCCTTTCACTTACTAGGGGTGTGACCAATGTA TCCAATCTCCAGACGGGAAGCATCCACACTCCGGCCTTTCACTTACTAGGGGTGTGACCAATGTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62630396..62630660 26863196 MeRIP-seq:(Medium) rs577489001 Functional Loss SNV dbSNP153 33..33 33 - - - 99005 RMVar_ID_99005 Human_SNP_ID_629589868 m1A Human chr17 + 62652605 62652604 62652605 GGCTCTTGGGCTGTTTATTTTGGCTGCGGGCTAGCAGACGGCGCCAGGGGCAGCGGCCACGCAGA GGCTCTTGGGCTGTTTATTTTGGCTGCGGGCT_GCAGACGGCGCCAGGGGCAGCGGCCACGCAGA TA T MRC2 Ensembl:ENSG00000011028 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:62652601..62652951 26863196 MeRIP-seq:(Medium) rs1568055127 Functional Loss DEL dbSNP153 33..33 33 - - - 99006 RMVar_ID_99006 Human_SNP_ID_629591147 m1A Human chr17 + 62657883 62657883 62657883 CTCTTTTCATTGAGGGCCCAGGCCCACCGGCCACTTCGGGTGGAAAATGCTCTCAAGAACCCCCT CTCTTTTCATTGAGGGCCCAGGCCCACCGGCCGCTTCGGGTGGAAAATGCTCTCAAGAACCCCCT A G MRC2 Ensembl:ENSG00000011028 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62657878..62657966 26863196 MeRIP-seq:(Medium) rs554575943 Functional Loss SNV dbSNP153 33..33 33 - - - 99007 RMVar_ID_99007 Human_SNP_ID_629591148 m1A Human chr17 + 62657883 62657883 62657883 CTCTTTTCATTGAGGGCCCAGGCCCACCGGCCACTTCGGGTGGAAAATGCTCTCAAGAACCCCCT CTCTTTTCATTGAGGGCCCAGGCCCACCGGCCTCTTCGGGTGGAAAATGCTCTCAAGAACCCCCT A T MRC2 Ensembl:ENSG00000011028 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62657878..62657966 26863196 MeRIP-seq:(Medium) rs554575943 Functional Loss SNV dbSNP153 33..33 33 - - - 99008 RMVar_ID_99008 Human_SNP_ID_629593249 m1A Human chr17 + 62666202 62666200 62666203 CGGCTGCACCAGCACGGGCCGCGAGGATGGTCACCTGTGGTGTGCCACCACCCAGGACTACGGCA CGGCTGCACCAGCACGGGCCGCGAGGATGGT___CTGTGGTGTGCCACCACCCAGGACTACGGCA TCAC T MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62666070..62666300 26863196 MeRIP-seq:(Medium) rs762848289 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5577635 Human_Splice_Rec_1850805,Human_Splice_Rec_1850863 Human_miRNA_ID_2056598,Human_miRNA_ID_2891105 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_308737,RMVar_hsa_circ_372334,RMVar_hsa_circ_323827,RMVar_hsa_circ_114480,RMVar_hsa_circ_345839,RMVar_hsa_circ_37407,RMVar_hsa_circ_186231 99009 RMVar_ID_99009 Human_SNP_ID_629593488 m1A Human chr17 - 62666869 62666869 62666869 GCTGCCCTGCGCCCCCAACCTTGTGCCTCACCACTCTCCCAGTTGAGGTACTTGAGGGGCGAGTT GCTGCCCTGCGCCCCCAACCTTGTGCCTCACCCCTCTCCCAGTTGAGGTACTTGAGGGGCGAGTT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:62666826..62666875 26863196 MeRIP-seq:(Medium) rs747607974 Functional Loss SNV dbSNP153 33..33 33 - - - 99010 RMVar_ID_99010 Human_SNP_ID_629593698 m1A Human chr17 + 62667519 62667519 62667519 TGTGTGCAAGAAGAAGCCCAACGCCACGGCCGAGCCCACCCCTCCAGGTGAGCCAGGGACTGTGC TGTGTGCAAGAAGAAGCCCAACGCCACGGCCGGGCCCACCCCTCCAGGTGAGCCAGGGACTGTGC A G MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:62667376..62667628 26863196 MeRIP-seq:(Medium) rs777898019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1850811,Human_Splice_Rec_1850869 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_308737,RMVar_hsa_circ_372334,RMVar_hsa_circ_323827,RMVar_hsa_circ_114480,RMVar_hsa_circ_345839,RMVar_hsa_circ_37407,RMVar_hsa_circ_96956,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186231,RMVar_hsa_circ_75968,RMVar_hsa_circ_186232,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_79263,RMVar_hsa_circ_186234,RMVar_hsa_circ_186235,RMVar_hsa_circ_186236,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237 99011 RMVar_ID_99011 Human_SNP_ID_629593710 m1A Human chr17 - 62667535 62667535 62667535 CCCTCCCCACCCTGCGGCACAGTCCCTGGCTCACCTGGAGGGGTGGGCTCGGCCGTGGCGTTGGG CCCTCCCCACCCTGCGGCACAGTCCCTGGCTCTCCTGGAGGGGTGGGCTCGGCCGTGGCGTTGGG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:62667376..62667635 26863196 MeRIP-seq:(Medium) rs1216728530 Functional Loss SNV dbSNP153 33..33 33 - - - 99012 RMVar_ID_99012 Human_SNP_ID_629594815 m1A Human chr17 + 62671798 62671798 62671798 GGGGCGGTGGCGACCTGGTCAGCATCCACAGCATGGCGGAGCTGGAATTCATCACCAAGCAGATC GGGGCGGTGGCGACCTGGTCAGCATCCACAGCTTGGCGGAGCTGGAATTCATCACCAAGCAGATC A T MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:62671776..62671800 26863196 MeRIP-seq:(Medium) rs1484059295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130361 Human_Splice_Rec_1850813,Human_Splice_Rec_1850871 RMVar_hsa_circ_70974,RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_308737,RMVar_hsa_circ_372334,RMVar_hsa_circ_114480,RMVar_hsa_circ_37407,RMVar_hsa_circ_96956,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186231,RMVar_hsa_circ_75968,RMVar_hsa_circ_186232,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_186234,RMVar_hsa_circ_186235,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237,RMVar_hsa_circ_44124 99013 RMVar_ID_99013 Human_SNP_ID_629594854 m1A Human chr17 - 62671971 62671971 62671971 CCACCTCTGGGGGTGCAGCAGGAGAGGAGGGGAGAGAAAACATTGAGAGGTCAGCCTCAGCCACC CCACCTCTGGGGGTGCAGCAGGAGAGGAGGGGCGAGAAAACATTGAGAGGTCAGCCTCAGCCACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62671970..62672065 26863196 MeRIP-seq:(Medium) rs1392449671 Functional Loss SNV dbSNP153 33..33 33 - - - 99014 RMVar_ID_99014 Human_SNP_ID_629597082 m1A Human chr17 + 62680275 62680271 62680275 CCTCCCTGCAGTGGGTGGCCATGCAGTGCGACACACAGCTGGACTGGATCTGCAAGATCCCCAGA CCTCCCTGCAGTGGGTGGCCATGCAGTGC____CACAGCTGGACTGGATCTGCAAGATCCCCAGA CGACA C MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:62680226..62680275 26863196 MeRIP-seq:(Medium) rs1188489384 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_1850829 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_372334,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_186234,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237,RMVar_hsa_circ_97457,RMVar_hsa_circ_344011,RMVar_hsa_circ_29566,RMVar_hsa_circ_96335,RMVar_hsa_circ_76990,RMVar_hsa_circ_186240,RMVar_hsa_circ_186241,RMVar_hsa_circ_119621,RMVar_hsa_circ_186242,RMVar_hsa_circ_112482,RMVar_hsa_circ_186243,RMVar_hsa_circ_186244,RMVar_hsa_circ_320235 99015 RMVar_ID_99015 Human_SNP_ID_629597093 m1A Human chr17 + 62680305 62680305 62680305 ACACACAGCTGGACTGGATCTGCAAGATCCCCAGAGGTTGGCCGGAGTGGCGCTGGGGGACGCGG ACACACAGCTGGACTGGATCTGCAAGATCCCCGGAGGTTGGCCGGAGTGGCGCTGGGGGACGCGG A G MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62680157..62680323 26863196 MeRIP-seq:(Medium) rs1432218495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1850829 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_372334,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_186234,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237,RMVar_hsa_circ_97457,RMVar_hsa_circ_344011,RMVar_hsa_circ_29566,RMVar_hsa_circ_96335,RMVar_hsa_circ_76990,RMVar_hsa_circ_186240,RMVar_hsa_circ_186241,RMVar_hsa_circ_119621,RMVar_hsa_circ_186242,RMVar_hsa_circ_112482,RMVar_hsa_circ_186243,RMVar_hsa_circ_186244,RMVar_hsa_circ_320235 99016 RMVar_ID_99016 Human_SNP_ID_629597158 m1A Human chr17 + 62680452 62680452 62680452 ACGGACGTGCGGGAGCCCGACGACAGCCCTCAAGGTGAGCACCCCCCAGCCCATCCCGCTACCCA ACGGACGTGCGGGAGCCCGACGACAGCCCTCAGGGTGAGCACCCCCCAGCCCATCCCGCTACCCA A G MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:62680426..62680574 32194978 MeRIP-seq:(Medium) rs998783230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1850830,Human_Splice_Rec_1850831 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_372334,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_186234,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237,RMVar_hsa_circ_97457,RMVar_hsa_circ_344011,RMVar_hsa_circ_29566,RMVar_hsa_circ_96335,RMVar_hsa_circ_76990,RMVar_hsa_circ_186240,RMVar_hsa_circ_186241,RMVar_hsa_circ_119621,RMVar_hsa_circ_186242,RMVar_hsa_circ_112482,RMVar_hsa_circ_186243,RMVar_hsa_circ_186244,RMVar_hsa_circ_320235 99017 RMVar_ID_99017 Human_SNP_ID_629597721 m1A Human chr17 - 62682277 62682277 62682277 GCGTTTCTTTGGTGACGTTGCTGCGCTTGCAGATGTAGGGCAAGGCTGTCAGGCACCTCTGGTCC GCGTTTCTTTGGTGACGTTGCTGCGCTTGCAGGTGTAGGGCAAGGCTGTCAGGCACCTCTGGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:62682226..62682300 32194978 MeRIP-seq:(Medium) rs1406751621 Functional Loss SNV dbSNP153 33..33 33 - - - 99018 RMVar_ID_99018 Human_SNP_ID_629599160 m1A Human chr17 + 62688338 62688338 62688338 CCAGGAACCCCAGAGCCGGGTGAAGTGGTCAGAGGCACAGTTCTCCTGTGAACAGCAAGAGGCCC CCAGGAACCCCAGAGCCGGGTGAAGTGGTCAGGGGCACAGTTCTCCTGTGAACAGCAAGAGGCCC A G MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:62688276..62688400 32194978 MeRIP-seq:(Medium) rs1266508830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1850840,Human_Splice_Rec_1850841,Human_Splice_Rec_1850894,Human_Splice_Rec_1850895,Human_Splice_Rec_1850918,Human_Splice_Rec_1850919 Human_miRNA_ID_2073128,Human_miRNA_ID_2074810,Human_miRNA_ID_3064970 RMVar_hsa_circ_29566,RMVar_hsa_circ_96335,RMVar_hsa_circ_186241,RMVar_hsa_circ_320235,RMVar_hsa_circ_26121,RMVar_hsa_circ_95654,RMVar_hsa_circ_118196,RMVar_hsa_circ_186246,RMVar_hsa_circ_186247,RMVar_hsa_circ_85915,RMVar_hsa_circ_186248,RMVar_hsa_circ_370762,RMVar_hsa_circ_186250 99019 RMVar_ID_99019 Human_SNP_ID_629599564 m1A Human chr17 + 62689611 62689611 62689611 CCTACCTCAACGGCACCTTCCGGCTGCTTCAGAAGCCGCTGCGCTGGCACGATGCCCTCCTGCTG CCTACCTCAACGGCACCTTCCGGCTGCTTCAGGAGCCGCTGCGCTGGCACGATGCCCTCCTGCTG A G MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62689561..62689668 26863196 MeRIP-seq:(Medium) rs905480740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1850846,Human_Splice_Rec_1850900 RMVar_hsa_circ_29566,RMVar_hsa_circ_96335,RMVar_hsa_circ_186241,RMVar_hsa_circ_320235,RMVar_hsa_circ_95654,RMVar_hsa_circ_186246,RMVar_hsa_circ_85915,RMVar_hsa_circ_186248,RMVar_hsa_circ_370762,RMVar_hsa_circ_76381,RMVar_hsa_circ_186250,RMVar_hsa_circ_186251 99020 RMVar_ID_99020 Human_SNP_ID_629666903 m1A Human chr17 + 62966537 62966537 62966537 GAGCCGAGCCGAGGGGCGAGAGCTGGCCCCCGAGCCGCCGCTGACAGGAGCACCGCCGCGGGCTG GAGCCGAGCCGAGGGGCGAGAGCTGGCCCCCGGGCCGCCGCTGACAGGAGCACCGCCGCGGGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:62966453..62966690 26863196 MeRIP-seq:(Medium) rs935807778 Functional Loss SNV dbSNP153 33..33 33 - - - 99021 RMVar_ID_99021 Human_SNP_ID_629666909 m1A Human chr17 + 62966556 62966556 62966556 GAGCTGGCCCCCGAGCCGCCGCTGACAGGAGCACCGCCGCGGGCTGCGCTCGCCGGCTGCGAGGC GAGCTGGCCCCCGAGCCGCCGCTGACAGGAGCCCCGCCGCGGGCTGCGCTCGCCGGCTGCGAGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:62966506..62966783 26863196 MeRIP-seq:(Medium) rs1279250865 Functional Loss SNV dbSNP153 33..33 33 - - - 99022 RMVar_ID_99022 Human_SNP_ID_629666920 m1A Human chr17 + 62966612 62966594 62966613 CTGCGAGGCCCCGCCGCGCCGTTCCGGGGTGCAGACTCGCCGCGGGGCGTTGGAGGACTGCGAGG CTGCGAGGCCCCGCC___________________ACTCGCCGCGGGGCGTTGGAGGACTGCGAGG CGCGCCGTTCCGGGGTGCAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:62966574..62966681 26863196 MeRIP-seq:(Medium) rs1292627675 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_4444038 99023 RMVar_ID_99023 Human_SNP_ID_629685815 m1A Human chr17 + 63049795 63049795 63049795 GCTGGGATGGAAGCAGAGAAACCAGGTTAGTCATGAGGGTGGCTGGGACTCAGGGTGGTGGTAGC GCTGGGATGGAAGCAGAGAAACCAGGTTAGTCTTGAGGGTGGCTGGGACTCAGGGTGGTGGTAGC A T TANC2 Ensembl:ENSG00000170921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63049771..63049921 26863196 MeRIP-seq:(Medium) rs76044801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6631377 RMVar_hsa_circ_186253,RMVar_hsa_circ_36550,RMVar_hsa_circ_119468,RMVar_hsa_circ_306450,RMVar_hsa_circ_281653,RMVar_hsa_circ_37006,RMVar_hsa_circ_186254,RMVar_hsa_circ_186256,RMVar_hsa_circ_84303,RMVar_hsa_circ_186255 99024 RMVar_ID_99024 Human_SNP_ID_629776651 m1A Human chr17 - 63433929 63433929 63433929 AACACGTGGCACAAATGGGCCCGGCCTTTGGCAGAGGAGCAAGTGATATGATGTGTAAAGTATGT AACACGTGGCACAAATGGGCCCGGCCTTTGGCGGAGGAGCAAGTGATATGATGTGTAAAGTATGT T C CYB561 Ensembl:ENSG00000008283 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63433829..63434029 26863196 MeRIP-seq:(Medium) rs1448781363 Functional Loss SNV dbSNP153 33..33 33 - - - 99025 RMVar_ID_99025 Human_SNP_ID_629780352 m1A Human chr17 - 63446619 63446619 63446619 CCCAGGTCCTTCCGTGCGCAGTCGGGGCTCGCAAGGACGAATCCCGCGGCCCTCGAGGCAGGCCC CCCAGGTCCTTCCGTGCGCAGTCGGGGCTCGCGAGGACGAATCCCGCGGCCCTCGAGGCAGGCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:63446583..63446715 26863196 MeRIP-seq:(Medium) rs1409699364 Functional Loss SNV dbSNP153 33..33 33 - - - 99026 RMVar_ID_99026 Human_SNP_ID_629809781 m1A Human chr17 + 63550561 63550561 63550561 GTTGTTTGTCGCCGCATCCCCGCTTCCGGGTTAGGCCGTTCCTGCCCGCCCCCTCCTCTCCTCCC GTTGTTTGTCGCCGCATCCCCGCTTCCGGGTTCGGCCGTTCCTGCCCGCCCCCTCCTCTCCTCCC A C DCAF7 Ensembl:ENSG00000136485 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:63550510..63550697 26863196 MeRIP-seq:(Medium) rs375509503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465603,Human_RBP_ID_5420337,Human_RBP_ID_5441731,Human_RBP_ID_5466792,Human_RBP_ID_5497529 99027 RMVar_ID_99027 Human_SNP_ID_629809792 m1A Human chr17 - 63550621 63550621 63550621 GCCGGGTCAACAGTGGGCTGCGGCGGGCGGGGAGCCGAGCCTGAGATCTATGGGTCCGAAGGGAG GCCGGGTCAACAGTGGGCTGCGGCGGGCGGGGGGCCGAGCCTGAGATCTATGGGTCCGAAGGGAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:63550526..63550687 26863410 MeRIP-seq:(Medium) rs567134371 Functional Loss SNV dbSNP153 33..33 33 - - - 99028 RMVar_ID_99028 Human_SNP_ID_629809828 m1A Human chr17 + 63550729 63550729 63550729 GGAAGGAGATCTACAAGTATGAAGCGCCCTGGACAGTCTACGCGATGAACTGGAGTGTGCGGCCC GGAAGGAGATCTACAAGTATGAAGCGCCCTGGGCAGTCTACGCGATGAACTGGAGTGTGCGGCCC A G DCAF7 Ensembl:ENSG00000136485 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63550551..63550825 32194978 MeRIP-seq:(Medium) rs1464847698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237855,Human_RBP_ID_496805,Human_RBP_ID_1539753,Human_RBP_ID_1866540,Human_RBP_ID_4465604,Human_RBP_ID_6631765,Human_RBP_ID_9376526,Human_RBP_ID_13125576,Human_RBP_ID_18705612,Human_RBP_ID_23742601 Human_Splice_Rec_1851985,Human_Splice_Rec_1851997,Human_Splice_Rec_1852011,Human_Splice_Rec_1852015,Human_Splice_Rec_1852017 Human_miRNA_ID_311889 99029 RMVar_ID_99029 Human_SNP_ID_629821595 m1A Human chr17 + 63601282 63601282 63601282 TCCCCGCCGGGCACAACAAGTGGTCCAAAGTCAGGCACATCAAGGGTCCGAAGGACGTCGAAAGG TCCCCGCCGGGCACAACAAGTGGTCCAAAGTCGGGCACATCAAGGGTCCGAAGGACGTCGAAAGG A G TACO1 Ensembl:ENSG00000136463 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63600901..63601365 26863196 MeRIP-seq:(Medium) rs750664875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1539821,Human_RBP_ID_1866609,Human_RBP_ID_3533837,Human_RBP_ID_17898764 Human_Splice_Rec_1852029,Human_Splice_Rec_1852035 Human_miRNA_ID_2658868 99030 RMVar_ID_99030 Human_SNP_ID_629823086 m1A Human chr17 - 63607391 63607391 63607391 CATCCTCAGCTCCTGCTTCGATTGCCATCTCCAGGGCACGCTCTAGGTTCACAGCCTTCTTCTCT CATCCTCAGCTCCTGCTTCGATTGCCATCTCCGGGGCACGCTCTAGGTTCACAGCCTTCTTCTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63607341..63607475 26863196 MeRIP-seq:(Medium) rs1064793277 Functional Loss SNV dbSNP153 33..33 33 - - - 99031 RMVar_ID_99031 Human_SNP_ID_629826875 m1A Human chr17 + 63622476 63622476 63622476 AACGGTGGCCGGACGGAGAGACTGCGGGTCTGAGGGACTGGCGGGCGGGCGGGCCGAGCGGCGCC AACGGTGGCCGGACGGAGAGACTGCGGGTCTGGGGGACTGGCGGGCGGGCGGGCCGAGCGGCGCC A G MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr17:63622426..63622762;chr17:63622446..63622621;chr17:63622432..63622575 26863196 MeRIP-seq:(Medium) rs1321705882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237163,Human_RBP_ID_900482,Human_RBP_ID_4466695,Human_RBP_ID_5466796,Human_RBP_ID_9326780,Human_RBP_ID_18419695,Human_RBP_ID_18991950,Human_RBP_ID_26332171 Human_miRNA_ID_2210836 RMVar_hsa_circ_112584,RMVar_hsa_circ_186319 99032 RMVar_ID_99032 Human_SNP_ID_629826904 m1A Human chr17 + 63622559 63622559 63622559 CGAGCCCAGGAGCGCCCGGGATGTAGCGGGCCACCCTGCCGATGCCACAGCGCCCGGCCGCGGGC CGAGCCCAGGAGCGCCCGGGATGTAGCGGGCCCCCCTGCCGATGCCACAGCGCCCGGCCGCGGGC A C MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:63622460..63622568 26863410 MeRIP-seq:(Medium) rs979998518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464708,Human_RBP_ID_9378706,Human_RBP_ID_18412063,Human_RBP_ID_18419695,Human_RBP_ID_18991950 RMVar_hsa_circ_112584,RMVar_hsa_circ_186319 99033 RMVar_ID_99033 Human_SNP_ID_629852230 m1A Human chr17 - 63728336 63728336 63728336 TGTCATTTCTTGTAAGTAAACCAGAGCGAATCAGGGTGAGTGTTTTTCTATTCTTCTGGCTTTAC TGTCATTTCTTGTAAGTAAACCAGAGCGAATCGGGGTGAGTGTTTTTCTATTCTTCTGGCTTTAC T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63728334..63728401 26863196 MeRIP-seq:(Medium) rs772864848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19083500 Human_Splice_Rec_1852258,Human_Splice_Rec_1852284,Human_Splice_Rec_1852285,Human_Splice_Rec_1852304,Human_Splice_Rec_1852324,Human_Splice_Rec_1852325,Human_Splice_Rec_1852348,Human_Splice_Rec_1852349,Human_Splice_Rec_1852366,Human_Splice_Rec_1852386,Human_Splice_Rec_1852387,Human_Splice_Rec_1852408,Human_Splice_Rec_1852430,Human_Splice_Rec_1852431,Human_Splice_Rec_1852450,Human_Splice_Rec_1852451,Human_Splice_Rec_1852470,Human_Splice_Rec_1852486,Human_Splice_Rec_1852506,Human_Splice_Rec_1852507,Human_Splice_Rec_1852526,Human_Splice_Rec_1852527,Human_Splice_Rec_1852550,Human_Splice_Rec_1852551,Human_Splice_Rec_1852574,Human_Splice_Rec_1852575,Human_Splice_Rec_1852593,Human_Splice_Rec_1852610,Human_Splice_Rec_1852611,Human_Splice_Rec_1852630,Human_Splice_Rec_1852631,Human_Splice_Rec_1852652,Human_Splice_Rec_1852653,Human_Splice_Rec_1852688,Human_Splice_Rec_1852704,Human_Splice_Rec_1852705,Human_Splice_Rec_1852720,Human_Splice_Rec_1852721,Human_Splice_Rec_1852738,Human_Splice_Rec_1852784,Human_Splice_Rec_1852785,Human_Splice_Rec_1852804,Human_Splice_Rec_1852820,Human_Splice_Rec_1852821,Human_Splice_Rec_1852848,Human_Splice_Rec_1852849,Human_Splice_Rec_1852870,Human_Splice_Rec_1852871,Human_Splice_Rec_1852901,Human_Splice_Rec_1852914,Human_Splice_Rec_1852915,Human_Splice_Rec_1852935,Human_Splice_Rec_1852946,Human_Splice_Rec_1852947,Human_Splice_Rec_1852959,Human_Splice_Rec_1852974,Human_Splice_Rec_1852975,Human_Splice_Rec_1852984,Human_Splice_Rec_1853004,Human_Splice_Rec_1853012,Human_Splice_Rec_1853013,Human_Splice_Rec_1853022,Human_Splice_Rec_1853023,Human_Splice_Rec_1853038,Human_Splice_Rec_1853039,Human_Splice_Rec_1853044,Human_Splice_Rec_1853122,Human_Splice_Rec_1853123 RMVar_hsa_circ_5911,RMVar_hsa_circ_186328,RMVar_hsa_circ_378935,RMVar_hsa_circ_356953,RMVar_hsa_circ_328866,RMVar_hsa_circ_331431,RMVar_hsa_circ_186333,RMVar_hsa_circ_61642 99034 RMVar_ID_99034 Human_SNP_ID_629857292 m1A Human chr17 - 63746960 63746960 63746960 TTTCTCTATTTATTACCCCTTCTTTCTCTAGGAGGCTGCATTGAGGCGTGAGCAAAAGAAGTTGG TTTCTCTATTTATTACCCCTTCTTTCTCTAGGGGGCTGCATTGAGGCGTGAGCAAAAGAAGTTGG T C AC046185.1,CCDC47 Ensembl:ENSG00000125695,Ensembl:ENSG00000108588 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:63746951..63746975;chr17:63728328..63751998 26863196 MeRIP-seq:(Medium) rs1435809489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768223,Human_RBP_ID_6632549,Human_RBP_ID_22761633,Human_RBP_ID_22955803,Human_RBP_ID_25336203,Human_RBP_ID_26332173,Human_RBP_ID_27812989 Human_Splice_Rec_1853166,Human_Splice_Rec_1853192,Human_Splice_Rec_1853212 99035 RMVar_ID_99035 Human_SNP_ID_629858627 m1A Human chr17 - 63752001 63752001 63752001 GGAAGCAGCACAGTCTCGGCGGGAGGAGAAAAAAAGAGCAGAGAAGGAGCGAATCATGAATGAGG GGAAGCAGCACAGTCTCGGCGGGAGGAGAAAAGAAGAGCAGAGAAGGAGCGAATCATGAATGAGG T C AC046185.1,CCDC47 Ensembl:ENSG00000125695,Ensembl:ENSG00000108588 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63728372..63752067 26863196 MeRIP-seq:(Medium) rs769451441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376535,Human_RBP_ID_19079668 Human_Splice_Rec_1853121,Human_Splice_Rec_1853165,Human_Splice_Rec_1853191,Human_Splice_Rec_1853211 RMVar_hsa_circ_56797,RMVar_hsa_circ_302072,RMVar_hsa_circ_357986,RMVar_hsa_circ_360702,RMVar_hsa_circ_339309,RMVar_hsa_circ_295056,RMVar_hsa_circ_186334,RMVar_hsa_circ_186335,RMVar_hsa_circ_186336 99036 RMVar_ID_99036 Human_SNP_ID_629864991 m1A Human chr17 + 63774367 63774367 63774367 CGCCCGCGGTTGTAGCAGCTGCCGCTGCAGCCATAGCAGCAGGTTTGTGCGTGGGGTTTCTGGAC CGCCCGCGGTTGTAGCAGCTGCCGCTGCAGCCGTAGCAGCAGGTTTGTGCGTGGGGTTTCTGGAC A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:63774276..63774400 26863410 MeRIP-seq:(Medium) rs1050695831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822003,Human_RBP_ID_897772,Human_RBP_ID_3950944,Human_RBP_ID_4464714,Human_RBP_ID_5238047,Human_RBP_ID_5318566,Human_RBP_ID_5364671,Human_RBP_ID_5467401,Human_RBP_ID_5525760,Human_RBP_ID_8232435,Human_RBP_ID_8941842,Human_RBP_ID_9327396,Human_RBP_ID_9353437,Human_RBP_ID_9376550,Human_RBP_ID_18419697,Human_RBP_ID_18988971,Human_RBP_ID_22959262,Human_RBP_ID_26333686,Human_RBP_ID_27812993 Human_Splice_Rec_1853253,Human_Splice_Rec_1853289,Human_Splice_Rec_1853321,Human_Splice_Rec_1853353 RMVar_hsa_circ_186344,RMVar_hsa_circ_94895 99037 RMVar_ID_99037 Human_SNP_ID_629872305 m1A Human chr17 + 63800573 63800573 63800573 AATATGATAGTGACGGAAATCCAATTGCACCTACCAAAAAAATCATTGATCCTCTTCCCCCCATT AATATGATAGTGACGGAAATCCAATTGCACCTGCCAAAAAAATCATTGATCCTCTTCCCCCCATT A G DDX42 Ensembl:ENSG00000198231 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63800522..63805048 32194978 MeRIP-seq:(Medium) rs1346163895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376556,Human_RBP_ID_13128788,Human_RBP_ID_17493233 Human_Splice_Rec_1853263,Human_Splice_Rec_1853297,Human_Splice_Rec_1853329,Human_Splice_Rec_1853359,Human_Splice_Rec_1853391,Human_Splice_Rec_1853395,Human_Splice_Rec_1853403,Human_Splice_Rec_1853425,Human_Splice_Rec_1853449,Human_Splice_Rec_1853453 RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186350,RMVar_hsa_circ_304979,RMVar_hsa_circ_333259,RMVar_hsa_circ_355650,RMVar_hsa_circ_313887,RMVar_hsa_circ_73789,RMVar_hsa_circ_276350,RMVar_hsa_circ_186351,RMVar_hsa_circ_186348,RMVar_hsa_circ_186349,RMVar_hsa_circ_311609,RMVar_hsa_circ_311959,RMVar_hsa_circ_304956,RMVar_hsa_circ_30590,RMVar_hsa_circ_11550,RMVar_hsa_circ_96557,RMVar_hsa_circ_113299,RMVar_hsa_circ_186352,RMVar_hsa_circ_186353,RMVar_hsa_circ_99223,RMVar_hsa_circ_22339,RMVar_hsa_circ_186354,RMVar_hsa_circ_186355,RMVar_hsa_circ_186356,RMVar_hsa_circ_297818,RMVar_hsa_circ_374140,RMVar_hsa_circ_374559,RMVar_hsa_circ_54104,RMVar_hsa_circ_186357,RMVar_hsa_circ_186358 99038 RMVar_ID_99038 Human_SNP_ID_629876683 m1A Human chr17 + 63816919 63816919 63816919 TAATGAGCAATTATGAGGCCTACAAGCCTTCCACAGGAGCTATGGGAGATCGACTAACGGCAATG TAATGAGCAATTATGAGGCCTACAAGCCTTCCCCAGGAGCTATGGGAGATCGACTAACGGCAATG A C DDX42 Ensembl:ENSG00000198231 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:63816851..63816925 26863196 MeRIP-seq:(Medium) rs376711439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768730,Human_RBP_ID_1866813,Human_RBP_ID_6632894,Human_RBP_ID_8821214,Human_RBP_ID_9075167,Human_RBP_ID_9290274,Human_RBP_ID_18164815,Human_RBP_ID_18988983,Human_RBP_ID_19079675,Human_RBP_ID_22806168 Human_Splice_Rec_1853284,Human_Splice_Rec_1853285,Human_Splice_Rec_1853318,Human_Splice_Rec_1853319,Human_Splice_Rec_1853350,Human_Splice_Rec_1853351,Human_Splice_Rec_1853380,Human_Splice_Rec_1853381,Human_Splice_Rec_1853446,Human_Splice_Rec_1853447,Human_Splice_Rec_1853474,Human_Splice_Rec_1853475,Human_Splice_Rec_1853484,Human_Splice_Rec_1853485,Human_Splice_Rec_1853489 RMVar_hsa_circ_268145,RMVar_hsa_circ_30590,RMVar_hsa_circ_65544 99039 RMVar_ID_99039 Human_SNP_ID_629876934 m1A Human chr17 - 63817900 63817900 63817900 GCTCCGGCAGACGGGTAGGTCACAGGGGCACCACTGATGTTGCCAGTATTGCCAAAGCCTGGGAT GCTCCGGCAGACGGGTAGGTCACAGGGGCACCGCTGATGTTGCCAGTATTGCCAAAGCCTGGGAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:63817851..63818175 32194978 MeRIP-seq:(Medium) rs374283452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8460256 99040 RMVar_ID_99040 Human_SNP_ID_629877114 m1A Human chr17 + 63818297 63818295 63818298 AGATGGAGCCCAAGATGGAACCCAAAGTGGACAGCAGCAAGATGGACAAGGTGGACAGCAAGACA AGATGGAGCCCAAGATGGAACCCAAAGTGGA___CAGCAAGATGGACAAGGTGGACAGCAAGACA ACAG A DDX42 Ensembl:ENSG00000198231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr17:63817948..63818425;chr17:63818251..63818300 26863196,32194978 MeRIP-seq:(Medium) rs746662574 Functional Loss DEL dbSNP153,HGVD 32..34 33 - - - Human_RBP_ID_51009,Human_RBP_ID_497073,Human_RBP_ID_767623,Human_RBP_ID_5577658,Human_RBP_ID_6632909,Human_RBP_ID_8232441,Human_RBP_ID_13129246,Human_RBP_ID_22955895,Human_RBP_ID_26332201 RMVar_hsa_circ_268145 99041 RMVar_ID_99041 Human_SNP_ID_629877141 m1A Human chr17 + 63818371 63818371 63818371 GCTGACGGCTTTGCTGTCCCAGAGCCGCCTAAACGCAAGAAAAGTCGATGGGACAGTTAGAGGGG GCTGACGGCTTTGCTGTCCCAGAGCCGCCTAATCGCAAGAAAAGTCGATGGGACAGTTAGAGGGG A T DDX42 Ensembl:ENSG00000198231 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63818320..63818570 32194978 MeRIP-seq:(Medium) rs1567749292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22062290,Human_RBP_ID_26332202 RMVar_hsa_circ_268145 99042 RMVar_ID_99042 Human_SNP_ID_629877331 m1A Human chr17 - 63819068 63819068 63819068 TGGGTTTCTTGTTTAATTTTAAATTTAGCAATACCATCTCAAACCTGGAGCAATCCTGGAACAGT TGGGTTTCTTGTTTAATTTTAAATTTAGCAATGCCATCTCAAACCTGGAGCAATCCTGGAACAGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63819017..63819118 32194978 MeRIP-seq:(Medium) rs1384896015 Functional Loss SNV dbSNP153 33..33 33 - - - 99043 RMVar_ID_99043 Human_SNP_ID_629877611 m1A Human chr17 - 63819854 63819854 63819854 TTTCAAGGTGGTGGACTCAAGGATGAAGAAGGACCAAAGAGCACAGCAACGTAAGGAACAAAAGA TTTCAAGGTGGTGGACTCAAGGATGAAGAAGGGCCAAAGAGCACAGCAACGTAAGGAACAAAAGA T C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63819726..63820379 26863196 MeRIP-seq:(Medium) rs1383511337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47378,Human_RBP_ID_764756,Human_RBP_ID_822439,Human_RBP_ID_1866836,Human_RBP_ID_3534046,Human_RBP_ID_6632957,Human_RBP_ID_22959473,Human_RBP_ID_26332206 Human_miRNA_ID_2034549,Human_miRNA_ID_2035853,Human_miRNA_ID_3107881 RMVar_hsa_circ_101400,RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_102874,RMVar_hsa_circ_186367,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_186366 99044 RMVar_ID_99044 Human_SNP_ID_629877651 m1A Human chr17 + 63819928 63819928 63819928 ACTCCAGCTGGCCGGCGCACTTTGCGGCCCACACCTTTTTTGGCTACAACGTAGGTGACATGGCG ACTCCAGCTGGCCGGCGCACTTTGCGGCCCACGCCTTTTTTGGCTACAACGTAGGTGACATGGCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63819879..63820350 32194978 MeRIP-seq:(Medium) rs775922784 Functional Loss SNV dbSNP153 33..33 33 - - - 99045 RMVar_ID_99045 Human_SNP_ID_629877849 m1A Human chr17 - 63820292 63820292 63820292 ACGCTGGCGGGAAATCAATGCACGTCCCATCAAGAAGGTGGCTGAGGCTAAGGCTAGAAAGAAAA ACGCTGGCGGGAAATCAATGCACGTCCCATCAGGAAGGTGGCTGAGGCTAAGGCTAGAAAGAAAA T C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:63819730..63820366 26863196 MeRIP-seq:(Medium) rs777762622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821719 Human_Splice_Rec_1853529 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_102874,RMVar_hsa_circ_186367,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368 99046 RMVar_ID_99046 Human_SNP_ID_629878500 m1A Human chr17 + 63821792 63821792 63821792 ACTGCCTTTTCCTCCAGTGGTACCAGCAGTGGATTCTCCTCCTCCTCCTCCTCTTTATCATCTTG ACTGCCTTTTCCTCCAGTGGTACCAGCAGTGGGTTCTCCTCCTCCTCCTCCTCTTTATCATCTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63821625..63821861 26863196 MeRIP-seq:(Medium) rs776670113 Functional Loss SNV dbSNP153 33..33 33 - - - 99047 RMVar_ID_99047 Human_SNP_ID_629878502 m1A Human chr17 - 63821802 63821794 63821803 TACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTGGTACCACTGGAGG TACTGAAGTGCAAGATGATAAAGAGGAGGAG_________AATCCACTGCTGGTACCACTGGAGG TCTCCTCCTC T FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63821751..63821858 26863196 MeRIP-seq:(Medium) rs751549614 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_764759,Human_RBP_ID_822443,Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_5114812,Human_RBP_ID_6632966,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_18470082,Human_RBP_ID_26332212 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 Human_miRNA_ID_2506805,Human_miRNA_ID_3043375 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99048 RMVar_ID_99048 Human_SNP_ID_629878503 m1A Human chr17 - 63821802 63821794 63821803 TACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTGGTACCACTGGAGG TACTGAAGTGCAAGATGATAAAGAGGAGGAG______GAGAATCCACTGCTGGTACCACTGGAGG TCTCCTCCTC TCTC FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63821751..63821858 26863196 MeRIP-seq:(Medium) rs751549614 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_764759,Human_RBP_ID_822443,Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_5114812,Human_RBP_ID_6632966,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_18470082,Human_RBP_ID_26332212 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 Human_miRNA_ID_2506805,Human_miRNA_ID_3043375 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99049 RMVar_ID_99049 Human_SNP_ID_629878504 m1A Human chr17 - 63821802 63821794 63821803 TACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTGGTACCACTGGAGG TACTGAAGTGCAAGATGATAAAGAGGAGGAG___GAGGAGAATCCACTGCTGGTACCACTGGAGG TCTCCTCCTC TCTCCTC FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63821751..63821858 26863196 MeRIP-seq:(Medium) rs751549614 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_764759,Human_RBP_ID_822443,Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_5114812,Human_RBP_ID_6632966,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_18470082,Human_RBP_ID_26332212 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 Human_miRNA_ID_2506805,Human_miRNA_ID_3043375 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99050 RMVar_ID_99050 Human_SNP_ID_629878513 m1A Human chr17 - 63821815 63821804 63821816 ACAGTATGCGACTTACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTG ACAGTATGCGACTTACTGAAGTGCAAGATGA____________GGAGGAGGAGAATCCACTGCTG CTCCTCCTCTTTA C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:63821764..63821865 26863196 MeRIP-seq:(Medium) rs1318256400 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_4477299,Human_RBP_ID_5114812,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_17493241,Human_RBP_ID_18470082,Human_RBP_ID_26333705 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99051 RMVar_ID_99051 Human_SNP_ID_629878522 m1A Human chr17 - 63821815 63821812 63821815 ACAGTATGCGACTTACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTG ACAGTATGCGACTTACTGAAGTGCAAGATGAT___GAGGAGGAGGAGGAGGAGAATCCACTGCTG CTTT C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:63821764..63821865 26863196 MeRIP-seq:(Medium) rs777247915 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_4477299,Human_RBP_ID_5114812,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_17493241,Human_RBP_ID_18470082,Human_RBP_ID_26333705 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99052 RMVar_ID_99052 Human_SNP_ID_629878524 m1A Human chr17 - 63821815 63821815 63821815 ACAGTATGCGACTTACTGAAGTGCAAGATGATAAAGAGGAGGAGGAGGAGGAGAATCCACTGCTG ACAGTATGCGACTTACTGAAGTGCAAGATGATGAAGAGGAGGAGGAGGAGGAGAATCCACTGCTG T C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:63821764..63821865 26863196 MeRIP-seq:(Medium) rs1280162184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898672,Human_RBP_ID_1866841,Human_RBP_ID_4477299,Human_RBP_ID_5114812,Human_RBP_ID_8232442,Human_RBP_ID_9290276,Human_RBP_ID_9376586,Human_RBP_ID_17493241,Human_RBP_ID_18470082,Human_RBP_ID_26333705 Human_Splice_Rec_1853520,Human_Splice_Rec_1853521,Human_Splice_Rec_1853534,Human_Splice_Rec_1853535,Human_Splice_Rec_1853541,Human_Splice_Rec_1853548,Human_Splice_Rec_1853549 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_57227 99053 RMVar_ID_99053 Human_SNP_ID_629878655 m1A Human chr17 - 63822149 63822149 63822149 TGTTACACTTCAGTTATTAGAGGAAGTAACACAAGGGGATATGAGTGCAGCAGACACATTTCTGT TGTTACACTTCAGTTATTAGAGGAAGTAACACGAGGGGATATGAGTGCAGCAGACACATTTCTGT T C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63821963..63823601 26863196 MeRIP-seq:(Medium) rs1001759498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1866842,Human_RBP_ID_6632970,Human_RBP_ID_25335828 Human_Splice_Rec_1853518 RMVar_hsa_circ_107248,RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_186368,RMVar_hsa_circ_77678,RMVar_hsa_circ_57227,RMVar_hsa_circ_94075,RMVar_hsa_circ_186371,RMVar_hsa_circ_186372 99054 RMVar_ID_99054 Human_SNP_ID_629879177 m1A Human chr17 + 63823899 63823899 63823899 CTGCAATGGAAACCCCAGGCAGATCCATCTTCAGCTCCACACGCTCCCGCTGCTTTCTCTGCTCA CTGCAATGGAAACCCCAGGCAGATCCATCTTCGGCTCCACACGCTCCCGCTGCTTTCTCTGCTCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:63823848..63824228 32194978 MeRIP-seq:(Medium) rs1488882738 Functional Loss SNV dbSNP153 33..33 33 - - - 99055 RMVar_ID_99055 Human_SNP_ID_629879184 m1A Human chr17 + 63823931 63823913 63823931 AGCTCCACACGCTCCCGCTGCTTTCTCTGCTCACGCAACAGCTTCTTTTTCTTCCTGAGGGGGTG AGCTCCACACGCTCC__________________CGCAACAGCTTCTTTTTCTTCCTGAGGGGGTG CCGCTGCTTTCTCTGCTCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:63823781..63824369 26863196 MeRIP-seq:(Medium) rs1272219188 Functional Loss DEL dbSNP153 16..33 33 - - - 99056 RMVar_ID_99056 Human_SNP_ID_629879268 m1A Human chr17 + 63824091 63824091 63824091 CAAGCTCTACCCCAGCTCCTTTCACCTCTTCAATTCCGCCACCTCCTGGGCCTTCATTTCTGCCA CAAGCTCTACCCCAGCTCCTTTCACCTCTTCAGTTCCGCCACCTCCTGGGCCTTCATTTCTGCCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63823801..63824425 32194978 MeRIP-seq:(Medium) rs534211694 Functional Loss SNV dbSNP153 33..33 33 - - - 99057 RMVar_ID_99057 Human_SNP_ID_629879276 m1A Human chr17 - 63824105 63824105 63824105 ACTGAACCAGACCTTGGCAGAAATGAAGGCCCAGGAGGTGGCGGAATTGAAGAGGTGAAAGGAGC ACTGAACCAGACCTTGGCAGAAATGAAGGCCCGGGAGGTGGCGGAATTGAAGAGGTGAAAGGAGC T C FTSJ3 Ensembl:ENSG00000108592 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63823791..63824409 26863196 MeRIP-seq:(Medium) rs967209372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235878,Human_RBP_ID_822445,Human_RBP_ID_18988985,Human_RBP_ID_26332215,Human_RBP_ID_27814170 Human_Splice_Rec_1853515,Human_Splice_Rec_1853553 RMVar_hsa_circ_110022,RMVar_hsa_circ_186369,RMVar_hsa_circ_99624,RMVar_hsa_circ_186370,RMVar_hsa_circ_77678,RMVar_hsa_circ_57227,RMVar_hsa_circ_186372 99058 RMVar_ID_99058 Human_SNP_ID_629879810 m1A Human chr17 + 63825387 63825387 63825387 GAACGGAAAACCTTTGTGATGAAGCTGCCACCACGGGCCAAAAAGTCACAAGCCAAACGTAGAGC GAACGGAAAACCTTTGTGATGAAGCTGCCACCGCGGGCCAAAAAGTCACAAGCCAAACGTAGAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63825287..63825388 32194978 MeRIP-seq:(Medium) rs762905605 Functional Loss SNV dbSNP153 33..33 33 - - - 99059 RMVar_ID_99059 Human_SNP_ID_629880158 m1A Human chr17 - 63826254 63826251 63826255 GTTTATGCCTGTATCCAGCCTTATTGTGGGTGAGTAACGGACAGCTCTCCTTGGTGTTTTAAGGG GTTTATGCCTGTATCCAGCCTTATTGTGGGT____AACGGACAGCTCTCCTTGGTGTTTTAAGGG TACTC T FTSJ3 Ensembl:ENSG00000108592 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63826251..63826300 32194978 MeRIP-seq:(Medium) rs1225911948 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_19083537 Human_Splice_Rec_1853498,Human_Splice_Rec_1853560,Human_Splice_Rec_1853570,Human_Splice_Rec_1853580,Human_Splice_Rec_1853592,Human_Splice_Rec_1853602,Human_Splice_Rec_1853608 RMVar_hsa_circ_77678,RMVar_hsa_circ_186372,RMVar_hsa_circ_39460,RMVar_hsa_circ_186373,RMVar_hsa_circ_52955,RMVar_hsa_circ_101284,RMVar_hsa_circ_90990,RMVar_hsa_circ_125970,RMVar_hsa_circ_186375,RMVar_hsa_circ_186377 99060 RMVar_ID_99060 Human_SNP_ID_629881331 m1A Human chr17 + 63829937 63829937 63829937 GGGGAAGTAGTCCGGGCCATGGATAAGAAGAAAGTGTTGGTCAAGGTAAAAGCAGCATGACCCCA GGGGAAGTAGTCCGGGCCATGGATAAGAAGAAGGTGTTGGTCAAGGTAAAAGCAGCATGACCCCA A G PSMC5 Ensembl:ENSG00000087191 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:63829820..63829992;chr17:63829851..63829950;chr17:63829844..63829995 26863196 MeRIP-seq:(Medium) rs201733814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235744,Human_RBP_ID_278507,Human_RBP_ID_819474,Human_RBP_ID_1540029,Human_RBP_ID_1866864,Human_RBP_ID_3952813,Human_RBP_ID_8460294,Human_RBP_ID_8824913,Human_RBP_ID_9376598,Human_RBP_ID_17653919,Human_RBP_ID_19079689,Human_RBP_ID_26332223,Human_RBP_ID_27838815 Human_Splice_Rec_1853640,Human_Splice_Rec_1853641,Human_Splice_Rec_1853666,Human_Splice_Rec_1853667,Human_Splice_Rec_1853678,Human_Splice_Rec_1853679,Human_Splice_Rec_1853690,Human_Splice_Rec_1853691,Human_Splice_Rec_1853714,Human_Splice_Rec_1853715,Human_Splice_Rec_1853726,Human_Splice_Rec_1853727,Human_Splice_Rec_1853750,Human_Splice_Rec_1853751,Human_Splice_Rec_1853772,Human_Splice_Rec_1853773,Human_Splice_Rec_1853782,Human_Splice_Rec_1853783,Human_Splice_Rec_1853804,Human_Splice_Rec_1853805,Human_Splice_Rec_1853826,Human_Splice_Rec_1853827,Human_Splice_Rec_1853848,Human_Splice_Rec_1853849 RMVar_hsa_circ_86525,RMVar_hsa_circ_18431,RMVar_hsa_circ_186378 99061 RMVar_ID_99061 Human_SNP_ID_629881475 m1A Human chr17 - 63830390 63830390 63830390 ATCTGTTTGTCCAGTCCACCAATCATCTCATAAGTTGAATCTGGTACTTTCTCCACCATCATCAG ATCTGTTTGTCCAGTCCACCAATCATCTCATAGGTTGAATCTGGTACTTTCTCCACCATCATCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:63830261..63830503 26863196 MeRIP-seq:(Medium) rs991183205 Functional Loss SNV dbSNP153 33..33 33 - - - 99062 RMVar_ID_99062 Human_SNP_ID_629881714 m1A Human chr17 + 63831135 63831135 63831135 CGAAATCGACTCCATCGGCTCCTCGCGGCTGGAGGGGGGTTCTGGAGGGGACAGTGAAGTGCAGC CGAAATCGACTCCATCGGCTCCTCGCGGCTGGGGGGGGGTTCTGGAGGGGACAGTGAAGTGCAGC A G PSMC5 Ensembl:ENSG00000087191 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63831088..63831173 26863196 MeRIP-seq:(Medium) rs80345213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47113,Human_RBP_ID_235746,Human_RBP_ID_17654865,Human_RBP_ID_22443128,Human_RBP_ID_22500180,Human_RBP_ID_23743114 Human_Splice_Rec_1853648,Human_Splice_Rec_1853649,Human_Splice_Rec_1853684,Human_Splice_Rec_1853698,Human_Splice_Rec_1853722,Human_Splice_Rec_1853734,Human_Splice_Rec_1853735,Human_Splice_Rec_1853758,Human_Splice_Rec_1853759,Human_Splice_Rec_1853776,Human_Splice_Rec_1853777,Human_Splice_Rec_1853790,Human_Splice_Rec_1853791,Human_Splice_Rec_1853812,Human_Splice_Rec_1853813,Human_Splice_Rec_1853834,Human_Splice_Rec_1853835,Human_Splice_Rec_1853856,Human_Splice_Rec_1853857,Human_Splice_Rec_1853870,Human_Splice_Rec_1853871,Human_Splice_Rec_1853877,Human_Splice_Rec_1853882,Human_Splice_Rec_1853883 Human_miRNA_ID_2974830,Human_miRNA_ID_3008026 RMVar_hsa_circ_86525,RMVar_hsa_circ_186378 99063 RMVar_ID_99063 Human_SNP_ID_629882369 m1A Human chr17 + 63833154 63833154 63833154 AAGCAGCTCGTCTCTCCTCCTCAGGATTTCCAATCACATCAGTGATGATCTGCAAAGAGCCAGGA AAGCAGCTCGTCTCTCCTCCTCAGGATTTCCAGTCACATCAGTGATGATCTGCAAAGAGCCAGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63833103..63833695 32194978 MeRIP-seq:(Medium) rs1130111 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22058709 99064 RMVar_ID_99064 Human_SNP_ID_629885020 m1A Human chr17 + 63842588 63842588 63842588 GGTCCGGGCAGCATGCCGGGTCCCGCGGGGGGAGGCGGCGCTCCCAGGGCCGCAGCCACGGCGCC GGTCCGGGCAGCATGCCGGGTCCCGCGGGGGGCGGCGGCGCTCCCAGGGCCGCAGCCACGGCGCC A C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:63842487..63842588 26863410 MeRIP-seq:(Medium) rs1023727849 Functional Loss SNV dbSNP153 33..33 33 - - - 99065 RMVar_ID_99065 Human_SNP_ID_629885021 m1A Human chr17 + 63842588 63842588 63842588 GGTCCGGGCAGCATGCCGGGTCCCGCGGGGGGAGGCGGCGCTCCCAGGGCCGCAGCCACGGCGCC GGTCCGGGCAGCATGCCGGGTCCCGCGGGGGGGGGCGGCGCTCCCAGGGCCGCAGCCACGGCGCC A G - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:63842487..63842588 26863410 MeRIP-seq:(Medium) rs1023727849 Functional Loss SNV dbSNP153 33..33 33 - - - 99066 RMVar_ID_99066 Human_SNP_ID_629885030 m1A Human chr17 + 63842627 63842627 63842627 GCTCCCAGGGCCGCAGCCACGGCGCCGCCGCCAGGGCTTAGCGGGGGCAGCGGGAACCCGCCCGC GCTCCCAGGGCCGCAGCCACGGCGCCGCCGCCGGGGCTTAGCGGGGGCAGCGGGAACCCGCCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEK293T,Starvation treatment chr17:63842580..63842915;chr17:63842537..63842638 26863196,26863410 MeRIP-seq:(Medium) rs1195649351 Functional Loss SNV dbSNP153 33..33 33 - - - 99067 RMVar_ID_99067 Human_SNP_ID_629965839 m1A Human chr17 - 64130107 64130107 64130107 CTAGTCAGTTCTGCGTCCGCTGAGGCTCGGTCACCGCCTCGCTGTCGTCGCGGCGCCCCCGCCCC CTAGTCAGTTCTGCGTCCGCTGAGGCTCGGTCCCCGCCTCGCTGTCGTCGCGGCGCCCCCGCCCC T G ERN1 Ensembl:ENSG00000178607 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64130058..64130130 26863196 MeRIP-seq:(Medium) rs1015134735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445352 RMVar_hsa_circ_112217,RMVar_hsa_circ_186400 99068 RMVar_ID_99068 Human_SNP_ID_629970635 m1A Human chr17 - 64148448 64148410 64148449 GCCTTTTCATTTCGGTGACAGAAGAGATGGGCAGAGCAACTTATTTTCCACATTAAATTGTGCAT GCCTTTTCATTTCGGTGACAGAAGAGATGGG__________________________________ TCCCAAATGCACAATTTAATGTGGAAAATAAGTTGCTCTG T TEX2 Ensembl:ENSG00000136478 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:64148325..64148576 32194978 MeRIP-seq:(Medium) rs779437237 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_6633170,Human_RBP_ID_17377174,Human_RBP_ID_17493270,Human_RBP_ID_18295545,Human_RBP_ID_27455681,Human_RBP_ID_27561289 Human_miRNA_ID_461433,Human_miRNA_ID_881075,Human_miRNA_ID_927504,Human_miRNA_ID_1768004 99069 RMVar_ID_99069 Human_SNP_ID_629985293 m1A Human chr17 + 64213671 64213671 64213671 CTTCACAAGGCTCATGAAGGGTTTTGCACTGGAAAGGGTGGAGGTTGAGGCACTGGATGAGAGGA CTTCACAAGGCTCATGAAGGGTTTTGCACTGGTAAGGGTGGAGGTTGAGGCACTGGATGAGAGGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:64213620..64213761 26863196 MeRIP-seq:(Medium) rs1227063008 Functional Loss SNV dbSNP153 33..33 33 - - - 99070 RMVar_ID_99070 Human_SNP_ID_629985335 m1A Human chr17 - 64213782 64213782 64213782 CCCCAGGGTCGTCTTCGTCGGGGCCCTTAGCTAGCTCTCCCAGTGTGTCATCCCTTTCTGAGCAG CCCCAGGGTCGTCTTCGTCGGGGCCCTTAGCTGGCTCTCCCAGTGTGTCATCCCTTTCTGAGCAG T C TEX2 Ensembl:ENSG00000136478 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:64213627..64213842 26863196 MeRIP-seq:(Medium) rs782625522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144326,Human_RBP_ID_18941982 Human_miRNA_ID_1245780,Human_miRNA_ID_2600107 RMVar_hsa_circ_6062,RMVar_hsa_circ_115131,RMVar_hsa_circ_186417,RMVar_hsa_circ_186419,RMVar_hsa_circ_293634 99071 RMVar_ID_99071 Human_SNP_ID_629985392 m1A Human chr17 + 64213954 64213954 64213954 GACAGTCCATCTGCCAGGACAGGCGAGGCAGCAGGGCCGGCGGGGTCATGGCCAACTTGGGGTTC GACAGTCCATCTGCCAGGACAGGCGAGGCAGCGGGGCCGGCGGGGTCATGGCCAACTTGGGGTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:64213911..64214024 26863196 MeRIP-seq:(Medium) rs781839390 Functional Loss SNV dbSNP153 33..33 33 - - - 99072 RMVar_ID_99072 Human_SNP_ID_629985459 m1A Human chr17 + 64214136 64214136 64214136 GAAGTGAATGGCGATGGTATCTCGGGACACGGACCTCTGCACGTGCACTTTAGGGGCTGATGGTT GAAGTGAATGGCGATGGTATCTCGGGACACGGGCCTCTGCACGTGCACTTTAGGGGCTGATGGTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:64214087..64214245 26863196 MeRIP-seq:(Medium) rs1555632260 Functional Loss SNV dbSNP153 33..33 33 - - - 99073 RMVar_ID_99073 Human_SNP_ID_629985475 m1A Human chr17 - 64214164 64214164 64214164 CATGCCGAGAAAACCACTGACATGCCAAAACCATCAGCCCCTAAAGTGCACGTGCAGAGGTCCGT CATGCCGAGAAAACCACTGACATGCCAAAACCGTCAGCCCCTAAAGTGCACGTGCAGAGGTCCGT T C TEX2 Ensembl:ENSG00000136478 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:64213872..64214244 26863196 MeRIP-seq:(Medium) rs782071963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17898965 Human_Splice_Rec_1854642,Human_Splice_Rec_1854668,Human_Splice_Rec_1854690,Human_Splice_Rec_1854710,Human_Splice_Rec_1854764,Human_Splice_Rec_1854770 RMVar_hsa_circ_6062,RMVar_hsa_circ_115131,RMVar_hsa_circ_186417,RMVar_hsa_circ_186419,RMVar_hsa_circ_293634 99074 RMVar_ID_99074 Human_SNP_ID_629985476 m1A Human chr17 - 64214164 64214164 64214164 CATGCCGAGAAAACCACTGACATGCCAAAACCATCAGCCCCTAAAGTGCACGTGCAGAGGTCCGT CATGCCGAGAAAACCACTGACATGCCAAAACCCTCAGCCCCTAAAGTGCACGTGCAGAGGTCCGT T G TEX2 Ensembl:ENSG00000136478 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:64213872..64214244 26863196 MeRIP-seq:(Medium) rs782071963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17898965 Human_Splice_Rec_1854642,Human_Splice_Rec_1854668,Human_Splice_Rec_1854690,Human_Splice_Rec_1854710,Human_Splice_Rec_1854764,Human_Splice_Rec_1854770 RMVar_hsa_circ_6062,RMVar_hsa_circ_115131,RMVar_hsa_circ_186417,RMVar_hsa_circ_186419,RMVar_hsa_circ_293634 99075 RMVar_ID_99075 Human_SNP_ID_629985479 m1A Human chr17 - 64214175 64214175 64214175 TGTATGGTCGCCATGCCGAGAAAACCACTGACATGCCAAAACCATCAGCCCCTAAAGTGCACGTG TGTATGGTCGCCATGCCGAGAAAACCACTGACGTGCCAAAACCATCAGCCCCTAAAGTGCACGTG T C TEX2 Ensembl:ENSG00000136478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64213896..64214250 26863196 MeRIP-seq:(Medium) rs562126347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465619 Human_Splice_Rec_1854642,Human_Splice_Rec_1854668,Human_Splice_Rec_1854690,Human_Splice_Rec_1854710,Human_Splice_Rec_1854764,Human_Splice_Rec_1854770 Human_miRNA_ID_416152 RMVar_hsa_circ_6062,RMVar_hsa_circ_115131,RMVar_hsa_circ_186417,RMVar_hsa_circ_186419,RMVar_hsa_circ_293634 99076 RMVar_ID_99076 Human_SNP_ID_630048197 m1A Human chr17 + 64496987 64496987 64496987 ACACGAGAGCGCATCTCTCTCCGAAGTTAAAGAGCACACTCTCCCATCACTCAACGGATCCCAAC ACACGAGAGCGCATCTCTCTCCGAAGTTAAAGGGCACACTCTCCCATCACTCAACGGATCCCAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:64496604..64497050;chr17:64496626..64497050 26863196 MeRIP-seq:(Medium) rs1555669690 Functional Loss SNV dbSNP153 33..33 33 - - - 99077 RMVar_ID_99077 Human_SNP_ID_630049559 m1A Human chr17 - 64500241 64500241 64500241 GCGGGCAAAAGGGGTGGATTTAATACCTTTAGAGACAGGGAAAATTATGACAGAGGTTACTCTAG GCGGGCAAAAGGGGTGGATTTAATACCTTTAGGGACAGGGAAAATTATGACAGAGGTTACTCTAG T C DDX5 Ensembl:ENSG00000108654 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:64500190..64500322 26863196 MeRIP-seq:(Medium) rs1329466514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50448,Human_RBP_ID_1010004,Human_RBP_ID_1288288,Human_RBP_ID_1540137,Human_RBP_ID_1866971,Human_RBP_ID_2519263,Human_RBP_ID_3534202,Human_RBP_ID_6633446,Human_RBP_ID_8460459,Human_RBP_ID_9075245,Human_RBP_ID_9876202,Human_RBP_ID_13130535,Human_RBP_ID_17898998,Human_RBP_ID_18706055,Human_RBP_ID_22219256,Human_RBP_ID_22500197,Human_RBP_ID_22806211,Human_RBP_ID_22956000,Human_RBP_ID_24480585,Human_RBP_ID_25316886,Human_RBP_ID_26645253,Human_RBP_ID_26968837,Human_RBP_ID_27258305,Human_RBP_ID_27668702 Human_Splice_Rec_1855062,Human_Splice_Rec_1855084,Human_Splice_Rec_1855106,Human_Splice_Rec_1855128,Human_Splice_Rec_1855150,Human_Splice_Rec_1855174,Human_Splice_Rec_1855180,Human_Splice_Rec_1855186,Human_Splice_Rec_1855190 Human_miRNA_ID_976002 RMVar_hsa_circ_186431 99078 RMVar_ID_99078 Human_SNP_ID_630050548 m1A Human chr17 + 64503323 64503323 64503323 TTTCCACACTCTAAAAAGTCAATCAGTCTTCCAGGTGTTGCAATACAGATTTCCACACCTTTAAT TTTCCACACTCTAAAAAGTCAATCAGTCTTCCCGGTGTTGCAATACAGATTTCCACACCTTTAAT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:64503272..64503373 32194978 MeRIP-seq:(Medium) rs201938017 Functional Loss SNV dbSNP153 33..33 33 - - - 99079 RMVar_ID_99079 Human_SNP_ID_630050649 m1A Human chr17 + 64503551 64503551 64503551 GCTACTTGCTGCACCTGTTGGGCCAGTTCCCGAGTTGGTGCCAGCACCAAACACTAAGGAAAGAG GCTACTTGCTGCACCTGTTGGGCCAGTTCCCGCGTTGGTGCCAGCACCAAACACTAAGGAAAGAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:64503426..64503621 32194978 MeRIP-seq:(Medium) rs917596854 Functional Loss SNV dbSNP153 33..33 33 - - - 99080 RMVar_ID_99080 Human_SNP_ID_630051023 m1A Human chr17 - 64504316 64504316 64504316 ATTTTAAGACTGTTATAATTTGTTTTGCAGCAAGAGGTGGAAACATACAGAAGAAGCAAGGAAAT ATTTTAAGACTGTTATAATTTGTTTTGCAGCATGAGGTGGAAACATACAGAAGAAGCAAGGAAAT T A DDX5 Ensembl:ENSG00000108654 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64504279..64504356 26863196 MeRIP-seq:(Medium) rs781996716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47434,Human_RBP_ID_235898,Human_RBP_ID_764797,Human_RBP_ID_904058,Human_RBP_ID_1540247,Human_RBP_ID_2519336,Human_RBP_ID_3952824,Human_RBP_ID_4445614,Human_RBP_ID_18706169,Human_RBP_ID_22219301,Human_RBP_ID_22659171,Human_RBP_ID_25336226,Human_RBP_ID_26332252 Human_Splice_Rec_1855042,Human_Splice_Rec_1855043,Human_Splice_Rec_1855086,Human_Splice_Rec_1855087,Human_Splice_Rec_1855110,Human_Splice_Rec_1855111,Human_Splice_Rec_1855132,Human_Splice_Rec_1855133,Human_Splice_Rec_1855154,Human_Splice_Rec_1855155,Human_Splice_Rec_1855240,Human_Splice_Rec_1855241,Human_Splice_Rec_1855248,Human_Splice_Rec_1855249,Human_Splice_Rec_1855256,Human_Splice_Rec_1855257,Human_Splice_Rec_1855266,Human_Splice_Rec_1855267,Human_Splice_Rec_1855273,Human_Splice_Rec_1855278,Human_Splice_Rec_1855279,Human_Splice_Rec_1855286,Human_Splice_Rec_1855287,Human_Splice_Rec_1855294,Human_Splice_Rec_1855295,Human_Splice_Rec_1855300,Human_Splice_Rec_1855301,Human_Splice_Rec_1855306,Human_Splice_Rec_1855307,Human_Splice_Rec_1855314,Human_Splice_Rec_1855315,Human_Splice_Rec_1855320,Human_Splice_Rec_1855321 RMVar_hsa_circ_51270,RMVar_hsa_circ_59606,RMVar_hsa_circ_60060,RMVar_hsa_circ_320284,RMVar_hsa_circ_291366,RMVar_hsa_circ_186435,RMVar_hsa_circ_362799,RMVar_hsa_circ_363186,RMVar_hsa_circ_57679,RMVar_hsa_circ_59682,RMVar_hsa_circ_100155,RMVar_hsa_circ_310253,RMVar_hsa_circ_375885,RMVar_hsa_circ_186444,RMVar_hsa_circ_75485,RMVar_hsa_circ_186443,RMVar_hsa_circ_71047,RMVar_hsa_circ_56471 99081 RMVar_ID_99081 Human_SNP_ID_630051024 m1A Human chr17 - 64504316 64504316 64504316 ATTTTAAGACTGTTATAATTTGTTTTGCAGCAAGAGGTGGAAACATACAGAAGAAGCAAGGAAAT ATTTTAAGACTGTTATAATTTGTTTTGCAGCAGGAGGTGGAAACATACAGAAGAAGCAAGGAAAT T C DDX5 Ensembl:ENSG00000108654 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64504279..64504356 26863196 MeRIP-seq:(Medium) rs781996716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47434,Human_RBP_ID_235898,Human_RBP_ID_764797,Human_RBP_ID_904058,Human_RBP_ID_1540247,Human_RBP_ID_2519336,Human_RBP_ID_3952824,Human_RBP_ID_4445614,Human_RBP_ID_18706169,Human_RBP_ID_22219301,Human_RBP_ID_22659171,Human_RBP_ID_25336226,Human_RBP_ID_26332252 Human_Splice_Rec_1855042,Human_Splice_Rec_1855043,Human_Splice_Rec_1855086,Human_Splice_Rec_1855087,Human_Splice_Rec_1855110,Human_Splice_Rec_1855111,Human_Splice_Rec_1855132,Human_Splice_Rec_1855133,Human_Splice_Rec_1855154,Human_Splice_Rec_1855155,Human_Splice_Rec_1855240,Human_Splice_Rec_1855241,Human_Splice_Rec_1855248,Human_Splice_Rec_1855249,Human_Splice_Rec_1855256,Human_Splice_Rec_1855257,Human_Splice_Rec_1855266,Human_Splice_Rec_1855267,Human_Splice_Rec_1855273,Human_Splice_Rec_1855278,Human_Splice_Rec_1855279,Human_Splice_Rec_1855286,Human_Splice_Rec_1855287,Human_Splice_Rec_1855294,Human_Splice_Rec_1855295,Human_Splice_Rec_1855300,Human_Splice_Rec_1855301,Human_Splice_Rec_1855306,Human_Splice_Rec_1855307,Human_Splice_Rec_1855314,Human_Splice_Rec_1855315,Human_Splice_Rec_1855320,Human_Splice_Rec_1855321 RMVar_hsa_circ_51270,RMVar_hsa_circ_59606,RMVar_hsa_circ_60060,RMVar_hsa_circ_320284,RMVar_hsa_circ_291366,RMVar_hsa_circ_186435,RMVar_hsa_circ_362799,RMVar_hsa_circ_363186,RMVar_hsa_circ_57679,RMVar_hsa_circ_59682,RMVar_hsa_circ_100155,RMVar_hsa_circ_310253,RMVar_hsa_circ_375885,RMVar_hsa_circ_186444,RMVar_hsa_circ_75485,RMVar_hsa_circ_186443,RMVar_hsa_circ_71047,RMVar_hsa_circ_56471 99082 RMVar_ID_99082 Human_SNP_ID_630051262 m1A Human chr17 + 64504825 64504825 64504825 TTCCAGATAAGGGCCCTGCCCTACTTCCTCCAAATCGAGGTGCACCAAACCTGGAATGAAAAAAA TTCCAGATAAGGGCCCTGCCCTACTTCCTCCACATCGAGGTGCACCAAACCTGGAATGAAAAAAA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:64504801..64504825 26863196 MeRIP-seq:(Medium) rs782215315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107620,RMVar_hsa_circ_186450 99083 RMVar_ID_99083 Human_SNP_ID_630052032 m1A Human chr17 - 64506167 64506167 64506167 CGTCATCGAGGCCATTTCCAGCGACTTGTCGCACGCTTTTCTATATACTTCGTTCCCCGCCAACC CGTCATCGAGGCCATTTCCAGCGACTTGTCGCGCGCTTTTCTATATACTTCGTTCCCCGCCAACC T C DDX5 Ensembl:ENSG00000108654 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:64506083..64506275 26863196 MeRIP-seq:(Medium) rs1555672572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497417,Human_RBP_ID_1183720,Human_RBP_ID_1540266,Human_RBP_ID_1867027,Human_RBP_ID_4445620,Human_RBP_ID_5441753,Human_RBP_ID_8460545,Human_RBP_ID_18706181,Human_RBP_ID_26812697,Human_RBP_ID_26968903,Human_RBP_ID_27455762 Human_Splice_Rec_1855039,Human_Splice_Rec_1855063,Human_Splice_Rec_1855085,Human_Splice_Rec_1855107,Human_Splice_Rec_1855129,Human_Splice_Rec_1855237,Human_Splice_Rec_1855245,Human_Splice_Rec_1855252,Human_Splice_Rec_1855253,Human_Splice_Rec_1855303,Human_Splice_Rec_1855310,Human_Splice_Rec_1855311,Human_Splice_Rec_1855323,Human_Splice_Rec_1855326,Human_Splice_Rec_1855327 RMVar_hsa_circ_291366 99084 RMVar_ID_99084 Human_SNP_ID_630052083 m1A Human chr17 + 64506229 64506227 64506230 ACGGCGAAGCCTTGCGGGGGCGGCAGCGGAGGAAGGACACCGATGACACCAGCCGAAGCTGCACT ACGGCGAAGCCTTGCGGGGGCGGCAGCGGAG___GGACACCGATGACACCAGCCGAAGCTGCACT GGAA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:64506015..64506300;chr17:64505999..64506275;chr17:64506031..64506300;chr17:64506044..64506300;chr17:64506034..64506300 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1395151172 Functional Loss DEL dbSNP153 32..34 33 - - - 99085 RMVar_ID_99085 Human_SNP_ID_630052083 m1A Human chr17 + 64506230 64506227 64506230 CGGCGAAGCCTTGCGGGGGCGGCAGCGGAGGAAGGACACCGATGACACCAGCCGAAGCTGCACTA CGGCGAAGCCTTGCGGGGGCGGCAGCGGAG___GGACACCGATGACACCAGCCGAAGCTGCACTA GGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:64506126..64506300 26863196 MeRIP-seq:(Medium) rs1395151172 Functional Loss DEL dbSNP153 31..33 33 - - - 99086 RMVar_ID_99086 Human_SNP_ID_630090903 m1A Human chr17 - 64661705 64661705 64661705 TCAATGATGAGTTGGGGGTCGGAGGAATGGGAAGGCCTAGTTCAGGGAGAGTAATTGGAAAACCA TCAATGATGAGTTGGGGGTCGGAGGAATGGGATGGCCTAGTTCAGGGAGAGTAATTGGAAAACCA T A SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:64661690..64661950 26863196 MeRIP-seq:(Medium) rs1270773021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3547569,Human_RBP_ID_8092743,Human_RBP_ID_8189785,Human_RBP_ID_9424125 RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 99087 RMVar_ID_99087 Human_SNP_ID_630090904 m1A Human chr17 - 64661705 64661705 64661705 TCAATGATGAGTTGGGGGTCGGAGGAATGGGAAGGCCTAGTTCAGGGAGAGTAATTGGAAAACCA TCAATGATGAGTTGGGGGTCGGAGGAATGGGAGGGCCTAGTTCAGGGAGAGTAATTGGAAAACCA T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:64661690..64661950 26863196 MeRIP-seq:(Medium) rs1270773021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3547569,Human_RBP_ID_8092743,Human_RBP_ID_8189785,Human_RBP_ID_9424125 RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 99088 RMVar_ID_99088 Human_SNP_ID_630091037 m1A Human chr17 - 64661987 64661987 64661987 GCACATCCGGGACCCTCCGGCCGTGGCGGCCGAGGCGCCGGCTGCTCGGGCCCCAGCCCCGGCCG GCACATCCGGGACCCTCCGGCCGTGGCGGCCGCGGCGCCGGCTGCTCGGGCCCCAGCCCCGGCCG T G SMURF2 Ensembl:ENSG00000108854 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:64661836..64661986 26863196 MeRIP-seq:(Medium) rs9907623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445701,Human_RBP_ID_18486640,Human_RBP_ID_26781657,Human_RBP_ID_27156724 RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 99089 RMVar_ID_99089 Human_SNP_ID_630091171 m1A Human chr17 - 64662269 64662269 64662269 GAGGGCGGGTGGAGGAGGAAGCGGCCGAGCCCAGAGTTCTGCTCCGGCGCCCCCGAGCACCGCCC GAGGGCGGGTGGAGGAGGAAGCGGCCGAGCCCTGAGTTCTGCTCCGGCGCCCCCGAGCACCGCCC T A SMURF2 Ensembl:ENSG00000108854 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:64662003..64662325;chr17:64661621..64662325 26863196 MeRIP-seq:(Medium) rs531367206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445714 99090 RMVar_ID_99090 Human_SNP_ID_630091172 m1A Human chr17 - 64662269 64662269 64662269 GAGGGCGGGTGGAGGAGGAAGCGGCCGAGCCCAGAGTTCTGCTCCGGCGCCCCCGAGCACCGCCC GAGGGCGGGTGGAGGAGGAAGCGGCCGAGCCCGGAGTTCTGCTCCGGCGCCCCCGAGCACCGCCC T C SMURF2 Ensembl:ENSG00000108854 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:64662003..64662325;chr17:64661621..64662325 26863196 MeRIP-seq:(Medium) rs531367206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445714 99091 RMVar_ID_99091 Human_SNP_ID_630151471 m1A Human chr17 - 64919020 64919020 64919020 AGCAGTAGCCGGAGAAAGCCGCCGCCGCCGCCAGCCCCACCCCAGCACCAGCGCCCCGGCCGGGG AGCAGTAGCCGGAGAAAGCCGCCGCCGCCGCCGGCCCCACCCCAGCACCAGCGCCCCGGCCGGGG T C LRRC37A3 Ensembl:ENSG00000176809 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:64918973..64919076 32194978 MeRIP-seq:(Medium) rs1257626079 Functional Loss SNV dbSNP153 33..33 33 - - - 99092 RMVar_ID_99092 Human_SNP_ID_630151669 m1A Human chr17 - 64919431 64919431 64919431 AAGAAACAAGATGGCGGCTGAAGGCGATCCGCAGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT AAGAAACAAGATGGCGGCTGAAGGCGATCCGCTGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT T A LRRC37A3 Ensembl:ENSG00000176809 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64919227..64919442 26863196 MeRIP-seq:(Medium) rs1309295391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13239092 Human_Splice_Rec_1855813,Human_Splice_Rec_1855923 99093 RMVar_ID_99093 Human_SNP_ID_630151670 m1A Human chr17 - 64919431 64919431 64919431 AAGAAACAAGATGGCGGCTGAAGGCGATCCGCAGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT AAGAAACAAGATGGCGGCTGAAGGCGATCCGCGGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT T C LRRC37A3 Ensembl:ENSG00000176809 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64919227..64919442 26863196 MeRIP-seq:(Medium) rs1309295391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13239092 Human_Splice_Rec_1855813,Human_Splice_Rec_1855923 99094 RMVar_ID_99094 Human_SNP_ID_630151671 m1A Human chr17 - 64919431 64919431 64919431 AAGAAACAAGATGGCGGCTGAAGGCGATCCGCAGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT AAGAAACAAGATGGCGGCTGAAGGCGATCCGCCGTGAGGCCCCAGCCATTCGGATTGAGCCTTCT T G LRRC37A3 Ensembl:ENSG00000176809 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64919227..64919442 26863196 MeRIP-seq:(Medium) rs1309295391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13239092 Human_Splice_Rec_1855813,Human_Splice_Rec_1855923 99095 RMVar_ID_99095 Human_SNP_ID_630151678 m1A Human chr17 - 64919437 64919437 64919437 TAACGGAAGAAACAAGATGGCGGCTGAAGGCGATCCGCAGTGAGGCCCCAGCCATTCGGATTGAG TAACGGAAGAAACAAGATGGCGGCTGAAGGCGTTCCGCAGTGAGGCCCCAGCCATTCGGATTGAG T A LRRC37A3 Ensembl:ENSG00000176809 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:64919326..64919461;chr17:64919289..64919459;chr17:64919337..64919457 26863196 MeRIP-seq:(Medium) rs1336465016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13239092 Human_Splice_Rec_1855813,Human_Splice_Rec_1855923 99096 RMVar_ID_99096 Human_SNP_ID_630151679 m1A Human chr17 - 64919437 64919437 64919437 TAACGGAAGAAACAAGATGGCGGCTGAAGGCGATCCGCAGTGAGGCCCCAGCCATTCGGATTGAG TAACGGAAGAAACAAGATGGCGGCTGAAGGCGCTCCGCAGTGAGGCCCCAGCCATTCGGATTGAG T G LRRC37A3 Ensembl:ENSG00000176809 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:64919326..64919461;chr17:64919289..64919459;chr17:64919337..64919457 26863196 MeRIP-seq:(Medium) rs1336465016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13239092 Human_Splice_Rec_1855813,Human_Splice_Rec_1855923 99097 RMVar_ID_99097 Human_SNP_ID_630164449 m1A Human chr17 - 64975050 64975050 64975050 CTCCTGACTTTTCTCACTGCCTTCGTTAATATAAAGATGAAGGCACACTCCACAACTTCCTTCTG CTCCTGACTTTTCTCACTGCCTTCGTTAATATTAAGATGAAGGCACACTCCACAACTTCCTTCTG T A AMZ2P1 Ensembl:ENSG00000214174 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64975031..64975180 26863196 MeRIP-seq:(Medium) rs1167883341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5098553,Human_RBP_ID_17899116 99098 RMVar_ID_99098 Human_SNP_ID_630164570 m1A Human chr17 + 64975524 64975516 64975524 GGCTGCCCCGCCCAGCTCTGACAGCACCTGCGAACCGCCCTGACCCAACAGGCCTCGACACCACT GGCTGCCCCGCCCAGCTCTGACAGC________ACCGCCCTGACCCAACAGGCCTCGACACCACT CACCTGCGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:64975309..64975678 26863196 MeRIP-seq:(Medium) rs1308096006 Functional Loss DEL dbSNP153 26..33 33 - - - 99099 RMVar_ID_99099 Human_SNP_ID_630184279 m1A Human chr17 + 65056640 65056640 65056640 CGCCGCCTCGGCGGGCCCCTCCGGCTCCCTCCACCTCCTCCTCCGGCGGCGGGCGGCTCCGGCAC CGCCGCCTCGGCGGGCCCCTCCGGCTCCCTCCCCCTCCTCCTCCGGCGGCGGGCGGCTCCGGCAC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:65056541..65056781 26863410 MeRIP-seq:(Medium) rs920594875 Functional Loss SNV dbSNP153 33..33 33 - - - 99100 RMVar_ID_99100 Human_SNP_ID_630195783 m1A Human chr17 - 65100874 65100874 65100874 TGGCTCGCCCCAGCCCTGGGTGGTCGACGGGGAGGCGGCTGGGCGGGGAGGGCGCGGGCCGGGCC TGGCTCGCCCCAGCCCTGGGTGGTCGACGGGGTGGCGGCTGGGCGGGGAGGGCGCGGGCCGGGCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:65100827..65100906 26863196 MeRIP-seq:(Medium) rs181494537 Functional Loss SNV dbSNP153 33..33 33 - - - 99101 RMVar_ID_99101 Human_SNP_ID_630448042 m1A Human chr17 + 66129249 66129249 66129249 ACACCCAATCACGACAGCTCACTTACCCCACTACATCTTTCTTCGTGCCTATTTCTGCCTCCAAT ACACCCAATCACGACAGCTCACTTACCCCACTTCATCTTTCTTCGTGCCTATTTCTGCCTCCAAT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66129202..66129411 26863196 MeRIP-seq:(Medium) rs1227638898 Functional Loss SNV dbSNP153 33..33 33 - - - 99102 RMVar_ID_99102 Human_SNP_ID_630462782 m1A Human chr17 + 66191971 66191971 66191971 TCCACTCAAGAACCTGGTGGGAGGGGCGGGGGAAGGAAATTCAGAAAAAAACGAGAACCTGGCAC TCCACTCAAGAACCTGGTGGGAGGGGCGGGGGGAGGAAATTCAGAAAAAAACGAGAACCTGGCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:66191966..66192080 26863196 MeRIP-seq:(Medium) rs900800449 Functional Loss SNV dbSNP153 33..33 33 - - - 99103 RMVar_ID_99103 Human_SNP_ID_630462798 m1A Human chr17 + 66192040 66192029 66192041 ACACGCAAGCTTTCCGCTCGGCCGCTGCCGCCAACGCCGCCGCCACCGCCGCCCCTGCCAAACGG ACACGCAAGCTTTCCGCTCGGC____________CGCCGCCGCCACCGCCGCCCCTGCCAAACGG CCGCTGCCGCCAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:66191856..66192084 26863196 MeRIP-seq:(Medium) rs1376878099 Functional Loss DEL dbSNP153 23..34 33 - - - 99104 RMVar_ID_99104 Human_SNP_ID_630462803 m1A Human chr17 + 66192040 66192040 66192040 ACACGCAAGCTTTCCGCTCGGCCGCTGCCGCCAACGCCGCCGCCACCGCCGCCCCTGCCAAACGG ACACGCAAGCTTTCCGCTCGGCCGCTGCCGCCGACGCCGCCGCCACCGCCGCCCCTGCCAAACGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:66191856..66192084 26863196 MeRIP-seq:(Medium) rs1048693003 Functional Loss SNV dbSNP153 33..33 33 - - - 99105 RMVar_ID_99105 Human_SNP_ID_630491433 m1A Human chr17 + 66302038 66302038 66302038 GGAGGTGAGCACCGGGCGGGAGGCTCCGGGGCAGGGGCTGCGCGTGGAGCCCACTCCCGGACGCG GGAGGTGAGCACCGGGCGGGAGGCTCCGGGGCGGGGGCTGCGCGTGGAGCCCACTCCCGGACGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:66302002..66302117 26863196 MeRIP-seq:(Medium) rs111783699 Functional Loss SNV dbSNP153 33..33 33 - - - 99106 RMVar_ID_99106 Human_SNP_ID_630491595 m1A Human chr17 - 66302378 66302348 66302378 GCCTTGCGGTGCTGGGAACACTGGGCAAGGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG GCCTTGCGGTGCTGGGAACACTGGGCAAGGGG______________________________CGG GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:66302303..66302462 26863196 MeRIP-seq:(Medium) rs1567760946 Functional Loss DEL dbSNP153 33..62 33 - - - 99107 RMVar_ID_99107 Human_SNP_ID_630491599 m1A Human chr17 - 66302378 66302360 66302378 GCCTTGCGGTGCTGGGAACACTGGGCAAGGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG GCCTTGCGGTGCTGGGAACACTGGGCAAGGGG__________________CGGCGGCGGCGGCGG GCCGCCGCCGCCGCCGCCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:66302303..66302462 26863196 MeRIP-seq:(Medium) rs1567760956 Functional Loss DEL dbSNP153 33..50 33 - - - 99108 RMVar_ID_99108 Human_SNP_ID_630491602 m1A Human chr17 - 66302378 66302363 66302378 GCCTTGCGGTGCTGGGAACACTGGGCAAGGGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGG GCCTTGCGGTGCTGGGAACACTGGGCAAGGGG_______________CGGCGGCGGCGGCGGCGG GCCGCCGCCGCCGCCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:66302303..66302462 26863196 MeRIP-seq:(Medium) rs1567760966 Functional Loss DEL dbSNP153 33..47 33 - - - 99109 RMVar_ID_99109 Human_SNP_ID_630491629 m1A Human chr17 - 66302435 66302435 66302435 GGGTGCGGCGGCGGCGGCGCTGAGCGGACCGGACCGAGTGCGGAGGAGGCAGCGAGTGCCTTGCG GGGTGCGGCGGCGGCGGCGCTGAGCGGACCGGTCCGAGTGCGGAGGAGGCAGCGAGTGCCTTGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:66302299..66302473 26863196 MeRIP-seq:(Medium) rs916065958 Functional Loss SNV dbSNP153 33..33 33 - - - 99110 RMVar_ID_99110 Human_SNP_ID_630491856 m1A Human chr17 - 66302840 66302840 66302840 GCCCGGGAAAACGTCAGCCATGGTCCCCCCCAACCACCTCTTGCCTCCGCCGGGGAGCTGCGGCC GCCCGGGAAAACGTCAGCCATGGTCCCCCCCAGCCACCTCTTGCCTCCGCCGGGGAGCTGCGGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:66302700..66302875 26863196 MeRIP-seq:(Medium) rs375669296 Functional Loss SNV dbSNP153 33..33 33 - - - 99111 RMVar_ID_99111 Human_SNP_ID_630515611 m1A Human chr17 - 66401537 66401537 66401537 TGGTCTGCAGAGAGCACAAAGCCGTCCACATCACTGAATGCGTCATGAGCTTTCCATCAATGATT TGGTCTGCAGAGAGCACAAAGCCGTCCACATCGCTGAATGCGTCATGAGCTTTCCATCAATGATT T C PRKCA-AS1 Ensembl:ENSG00000264630 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66401523..66401606 26863196 MeRIP-seq:(Medium) rs75901839 Functional Loss SNV dbSNP153 33..33 33 - - - 99112 RMVar_ID_99112 Human_SNP_ID_630568792 m1A Human chr17 + 66623997 66623997 66623997 GACCAGGGCAGGGAGTAGGGGGCTGTACCCAAAGACACTGAGGAAAACTTGTAGGGTGTCATCAA GACCAGGGCAGGGAGTAGGGGGCTGTACCCAACGACACTGAGGAAAACTTGTAGGGTGTCATCAA A C PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66623996..66624140 26863196 MeRIP-seq:(Medium) rs566075712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2631,RMVar_hsa_circ_113290,RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186581,RMVar_hsa_circ_186580,RMVar_hsa_circ_319983,RMVar_hsa_circ_186584,RMVar_hsa_circ_354618,RMVar_hsa_circ_347048,RMVar_hsa_circ_104911,RMVar_hsa_circ_313719,RMVar_hsa_circ_90409,RMVar_hsa_circ_186588,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_127655,RMVar_hsa_circ_186591,RMVar_hsa_circ_186592 99113 RMVar_ID_99113 Human_SNP_ID_630568793 m1A Human chr17 + 66623997 66623997 66623997 GACCAGGGCAGGGAGTAGGGGGCTGTACCCAAAGACACTGAGGAAAACTTGTAGGGTGTCATCAA GACCAGGGCAGGGAGTAGGGGGCTGTACCCAAGGACACTGAGGAAAACTTGTAGGGTGTCATCAA A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66623996..66624140 26863196 MeRIP-seq:(Medium) rs566075712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2631,RMVar_hsa_circ_113290,RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186581,RMVar_hsa_circ_186580,RMVar_hsa_circ_319983,RMVar_hsa_circ_186584,RMVar_hsa_circ_354618,RMVar_hsa_circ_347048,RMVar_hsa_circ_104911,RMVar_hsa_circ_313719,RMVar_hsa_circ_90409,RMVar_hsa_circ_186588,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_127655,RMVar_hsa_circ_186591,RMVar_hsa_circ_186592 99114 RMVar_ID_99114 Human_SNP_ID_630598506 m1A Human chr17 + 66748513 66748513 66748513 AGCACTAGACAGCCGTCTCGTTCTTGGACCCCAAGGAGGGCAAATGTTCATGAAGTCAGGGTGGC AGCACTAGACAGCCGTCTCGTTCTTGGACCCCGAGGAGGGCAAATGTTCATGAAGTCAGGGTGGC A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66748483..66748721 26863196 MeRIP-seq:(Medium) rs932843817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186580,RMVar_hsa_circ_186584,RMVar_hsa_circ_104911,RMVar_hsa_circ_186590,RMVar_hsa_circ_361688,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_186596,RMVar_hsa_circ_186597,RMVar_hsa_circ_102543,RMVar_hsa_circ_287989,RMVar_hsa_circ_186600,RMVar_hsa_circ_296584,RMVar_hsa_circ_186605,RMVar_hsa_circ_186604,RMVar_hsa_circ_109029,RMVar_hsa_circ_370841,RMVar_hsa_circ_338064,RMVar_hsa_circ_186609,RMVar_hsa_circ_186610,RMVar_hsa_circ_186608,RMVar_hsa_circ_118512,RMVar_hsa_circ_345043,RMVar_hsa_circ_186611,RMVar_hsa_circ_344500,RMVar_hsa_circ_186616,RMVar_hsa_circ_91033 99115 RMVar_ID_99115 Human_SNP_ID_630614081 m1A Human chr17 + 66809220 66809220 66809220 GAAGGCCATCATCTAGAAATGGGGTCAACCACAATTGTGTTAATTCCGTAGTGTCAGGGATTCTT GAAGGCCATCATCTAGAAATGGGGTCAACCACGATTGTGTTAATTCCGTAGTGTCAGGGATTCTT A G PRKCA Ensembl:ENSG00000154229 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs556631212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17899399 RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186580,RMVar_hsa_circ_186584,RMVar_hsa_circ_104911,RMVar_hsa_circ_186590,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_186596,RMVar_hsa_circ_186597,RMVar_hsa_circ_102543,RMVar_hsa_circ_186600,RMVar_hsa_circ_109029,RMVar_hsa_circ_186610,RMVar_hsa_circ_118512,RMVar_hsa_circ_186611,RMVar_hsa_circ_77618,RMVar_hsa_circ_76582,RMVar_hsa_circ_186616,RMVar_hsa_circ_91033,RMVar_hsa_circ_93591,RMVar_hsa_circ_186618,RMVar_hsa_circ_108416,RMVar_hsa_circ_186619,RMVar_hsa_circ_186620,RMVar_hsa_circ_186621 99116 RMVar_ID_99116 Human_SNP_ID_630652770 m1A Human chr17 + 66964599 66964599 66964599 GGCGCGGACCCGGAGCGCGGCGGCGGCGGGGGAGGCGCGGAGGGCGCAGGGCGGAGGCGCGGGCC GGCGCGGACCCGGAGCGCGGCGGCGGCGGGGGCGGCGCGGAGGGCGCAGGGCGGAGGCGCGGGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:66964488..66964802 26863196 MeRIP-seq:(Medium) rs1274971120 Functional Loss SNV dbSNP153 33..33 33 - - - 99117 RMVar_ID_99117 Human_SNP_ID_630689451 m1A Human chr17 - 67109511 67109511 67109511 AATCCCTAATCGCCACTTTCATCCCCTTCCCCAGCTACCAAGACCACCCTTTCCAATTCCACAGC AATCCCTAATCGCCACTTTCATCCCCTTCCCCGGCTACCAAGACCACCCTTTCCAATTCCACAGC T C HELZ Ensembl:ENSG00000198265 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:67109462..67109555 26863196 MeRIP-seq:(Medium) rs1206910436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17080817,Human_RBP_ID_17263644,Human_RBP_ID_18706753,Human_RBP_ID_18943499 Human_miRNA_ID_2685883 RMVar_hsa_circ_61471,RMVar_hsa_circ_366891,RMVar_hsa_circ_70522,RMVar_hsa_circ_352433,RMVar_hsa_circ_69269,RMVar_hsa_circ_94038,RMVar_hsa_circ_27252,RMVar_hsa_circ_83501,RMVar_hsa_circ_58646,RMVar_hsa_circ_282223,RMVar_hsa_circ_378021,RMVar_hsa_circ_69648,RMVar_hsa_circ_50307,RMVar_hsa_circ_114896,RMVar_hsa_circ_186628,RMVar_hsa_circ_186630,RMVar_hsa_circ_98606,RMVar_hsa_circ_186629,RMVar_hsa_circ_186631 99118 RMVar_ID_99118 Human_SNP_ID_630700510 m1A Human chr17 - 67156652 67156652 67156652 GGAGAGGAGGGCTGGAGAGTTAGAAGGGAAGCAGAGAAAGCTTGAGTCATGGAAGCTGAGGGGAG GGAGAGGAGGGCTGGAGAGTTAGAAGGGAAGCCGAGAAAGCTTGAGTCATGGAAGCTGAGGGGAG T G HELZ Ensembl:ENSG00000198265 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:67156601..67156730 26863196 MeRIP-seq:(Medium) rs192655794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23745209 RMVar_hsa_circ_69181,RMVar_hsa_circ_70522,RMVar_hsa_circ_65428,RMVar_hsa_circ_27252,RMVar_hsa_circ_83501,RMVar_hsa_circ_58646,RMVar_hsa_circ_378021,RMVar_hsa_circ_50307,RMVar_hsa_circ_114896,RMVar_hsa_circ_186628,RMVar_hsa_circ_186630,RMVar_hsa_circ_98606,RMVar_hsa_circ_186629,RMVar_hsa_circ_104418,RMVar_hsa_circ_47345,RMVar_hsa_circ_186633,RMVar_hsa_circ_354733,RMVar_hsa_circ_97056,RMVar_hsa_circ_7818,RMVar_hsa_circ_106975,RMVar_hsa_circ_186635,RMVar_hsa_circ_186637,RMVar_hsa_circ_364669,RMVar_hsa_circ_352284,RMVar_hsa_circ_11025,RMVar_hsa_circ_186639,RMVar_hsa_circ_53144,RMVar_hsa_circ_186643,RMVar_hsa_circ_186647,RMVar_hsa_circ_327881,RMVar_hsa_circ_354423,RMVar_hsa_circ_77333,RMVar_hsa_circ_186650,RMVar_hsa_circ_30551,RMVar_hsa_circ_186648,RMVar_hsa_circ_289232,RMVar_hsa_circ_372719,RMVar_hsa_circ_327869,RMVar_hsa_circ_108539,RMVar_hsa_circ_186652,RMVar_hsa_circ_186653,RMVar_hsa_circ_186654,RMVar_hsa_circ_186651 99119 RMVar_ID_99119 Human_SNP_ID_630721855 m1A Human chr17 + 67245372 67245372 67245372 GCTGGCCCCTTCCCCTCCCCCGGGCTGACGGCATTGAAAATTCACCCGCATTTTTAAAACGTGGC GCTGGCCCCTTCCCCTCCCCCGGGCTGACGGCGTTGAAAATTCACCCGCATTTTTAAAACGTGGC A G AC007448.5,AC007448.4 Ensembl:ENSG00000285877,Ensembl:ENSG00000266473 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:67245335..67245418 26863196 MeRIP-seq:(Medium) rs1379231596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497926 99120 RMVar_ID_99120 Human_SNP_ID_630752461 m1A Human chr17 - 67357505 67357505 67357505 GGAAAAGCAGACTCGTACTGTGAGTAGTTTACAGGGGAAAGCTCAGTTACCATTAATTTCATTGA GGAAAAGCAGACTCGTACTGTGAGTAGTTTACGGGGGAAAGCTCAGTTACCATTAATTTCATTGA T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:67357501..67357600 26863196 MeRIP-seq:(Medium) rs375575740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1867862,Human_RBP_ID_5362057,Human_RBP_ID_18706911,Human_RBP_ID_19079770,Human_RBP_ID_22416404 Human_Splice_Rec_1857104,Human_Splice_Rec_1857146,Human_Splice_Rec_1857168,Human_Splice_Rec_1857182,Human_Splice_Rec_1857190,Human_Splice_Rec_1857196 RMVar_hsa_circ_61716 99121 RMVar_ID_99121 Human_SNP_ID_630752476 m1A Human chr17 - 67357577 67357577 67357577 TTTTATTGTTCATTTTCATCTTTTGTTTTAGGAAGGAAGACTTCAAGAAGTCATTGAAACCCTTC TTTTATTGTTCATTTTCATCTTTTGTTTTAGGGAGGAAGACTTCAAGAAGTCATTGAAACCCTTC T C PSMD12 Ensembl:ENSG00000197170 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:67357551..67357600;chr17:67357401..67361147 26863196 MeRIP-seq:(Medium) rs139804019 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_900597,Human_RBP_ID_3535419,Human_RBP_ID_4465626,Human_RBP_ID_5362057,Human_RBP_ID_6637766,Human_RBP_ID_18992060,Human_RBP_ID_22656699,Human_RBP_ID_23745579,Human_RBP_ID_25335878 Human_Splice_Rec_1857104,Human_Splice_Rec_1857105,Human_Splice_Rec_1857146,Human_Splice_Rec_1857147,Human_Splice_Rec_1857168,Human_Splice_Rec_1857169,Human_Splice_Rec_1857182,Human_Splice_Rec_1857190,Human_Splice_Rec_1857191,Human_Splice_Rec_1857196,Human_Splice_Rec_1857197 RMVar_hsa_circ_61716 99122 RMVar_ID_99122 Human_SNP_ID_630754855 m1A Human chr17 - 67366459 67366459 67366459 ACGGGCGCATCGTCAAGATGGAGGTGGACTACAGCGCCACGGTGGATCAGCGCCTACCCGAGTGT ACGGGCGCATCGTCAAGATGGAGGTGGACTACGGCGCCACGGTGGATCAGCGCCTACCCGAGTGT T C PSMD12 Ensembl:ENSG00000197170 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:67366401..67366583;chr17:67366373..67366583 26863196 MeRIP-seq:(Medium) rs1435536086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1540753,Human_RBP_ID_4467333,Human_RBP_ID_5363073,Human_RBP_ID_8461335,Human_RBP_ID_9376705,Human_RBP_ID_18706925,Human_RBP_ID_18992061,Human_RBP_ID_22443135,Human_RBP_ID_26332277 Human_Splice_Rec_1857103,Human_Splice_Rec_1857123,Human_Splice_Rec_1857141,Human_Splice_Rec_1857167,Human_Splice_Rec_1857181,Human_Splice_Rec_1857187,Human_Splice_Rec_1857195 99123 RMVar_ID_99123 Human_SNP_ID_630754896 m1A Human chr17 - 67366536 67366536 67366536 GAGTGGTGGCCGAAGCAGGGGGACAGCAAGGGACGCTCAGGCGGGGACCATGGCGGACGGCGGCT GAGTGGTGGCCGAAGCAGGGGGACAGCAAGGGGCGCTCAGGCGGGGACCATGGCGGACGGCGGCT T C PSMD12 Ensembl:ENSG00000197170 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:67366401..67366600 26863196 MeRIP-seq:(Medium) rs762816165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51000,Human_RBP_ID_238300,Human_RBP_ID_4465627,Human_RBP_ID_6637937,Human_RBP_ID_22443136,Human_RBP_ID_26332278,Human_RBP_ID_27258615,Human_RBP_ID_27838519 99124 RMVar_ID_99124 Human_SNP_ID_630754900 m1A Human chr17 - 67366544 67366544 67366544 TGGGTGACGAGTGGTGGCCGAAGCAGGGGGACAGCAAGGGACGCTCAGGCGGGGACCATGGCGGA TGGGTGACGAGTGGTGGCCGAAGCAGGGGGACGGCAAGGGACGCTCAGGCGGGGACCATGGCGGA T C PSMD12 Ensembl:ENSG00000197170 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:67366361..67366639;chr17:67366349..67366627;chr17:67366401..67366605 26863196 MeRIP-seq:(Medium) rs1009133737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51000,Human_RBP_ID_238300,Human_RBP_ID_4465628,Human_RBP_ID_6637938,Human_RBP_ID_22443136,Human_RBP_ID_26332278,Human_RBP_ID_27838519 99125 RMVar_ID_99125 Human_SNP_ID_630754901 m1A Human chr17 - 67366567 67366544 67366568 GGGTGCGCGGGCAACTTCCGGTGTGGGTGACGAGTGGTGGCCGAAGCAGGGGGACAGCAAGGGAC GGGTGCGCGGGCAACTTCCGGTGTGGGTGAC________________________AGCAAGGGAC TGTCCCCCTGCTTCGGCCACCACTC T PSMD12 Ensembl:ENSG00000197170 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:67366467..67366577 26863410 MeRIP-seq:(Medium) rs1567964106 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_51000,Human_RBP_ID_767614,Human_RBP_ID_4465628,Human_RBP_ID_22443136,Human_RBP_ID_23745605,Human_RBP_ID_27838519 99126 RMVar_ID_99126 Human_SNP_ID_630754912 m1A Human chr17 - 67366567 67366567 67366567 GGGTGCGCGGGCAACTTCCGGTGTGGGTGACGAGTGGTGGCCGAAGCAGGGGGACAGCAAGGGAC GGGTGCGCGGGCAACTTCCGGTGTGGGTGACGCGTGGTGGCCGAAGCAGGGGGACAGCAAGGGAC T G PSMD12 Ensembl:ENSG00000197170 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:67366467..67366577 26863410 MeRIP-seq:(Medium) rs964659402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51000,Human_RBP_ID_767614,Human_RBP_ID_4465628,Human_RBP_ID_22443136,Human_RBP_ID_23745605,Human_RBP_ID_27838519 99127 RMVar_ID_99127 Human_SNP_ID_630757972 m1A Human chr17 + 67378149 67378149 67378149 CCCGCTTCCCGCCCCGGGGGTCCGCGGCCGGCAGGACCATGCTGCTGAAAGAGTACCGGATCTGC CCCGCTTCCCGCCCCGGGGGTCCGCGGCCGGCTGGACCATGCTGCTGAAAGAGTACCGGATCTGC A T PITPNC1 Ensembl:ENSG00000154217 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:67378099..67378174 26863196 MeRIP-seq:(Medium) rs534235557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466724 Human_Splice_Rec_1857199,Human_Splice_Rec_1857215,Human_Splice_Rec_1857229 99128 RMVar_ID_99128 Human_SNP_ID_630835643 m1A Human chr17 - 67692726 67692724 67692726 ACGGACAGAAATTCGGGTGCGTCTGTGGAGAGAGGGGTGGATGGAGCACTAGAAGGCGCACTGCG ACGGACAGAAATTCGGGTGCGTCTGTGGAGAG__GGGTGGATGGAGCACTAGAAGGCGCACTGCG CCT C lnc-C17orf58-8,lnc-C17orf58-8:2,lnc-C17orf58-8:3,lnc-C17orf58-8:4,lnc-C17orf58-8:5 RNACentral:URS0000D5D119,RNACentral:URS00008C3464,RNACentral:URS0000D5AFEC,RNACentral:URS00009B5976,RNACentral:URS0000D579D0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:67692675..67692740 26863196 MeRIP-seq:(Medium) rs778695419 Functional Loss DEL dbSNP153 33..34 33 - - - 99129 RMVar_ID_99129 Human_SNP_ID_630835644 m1A Human chr17 - 67692726 67692726 67692726 ACGGACAGAAATTCGGGTGCGTCTGTGGAGAGAGGGGTGGATGGAGCACTAGAAGGCGCACTGCG ACGGACAGAAATTCGGGTGCGTCTGTGGAGAGCGGGGTGGATGGAGCACTAGAAGGCGCACTGCG T G lnc-C17orf58-8,lnc-C17orf58-8:2,lnc-C17orf58-8:3,lnc-C17orf58-8:4,lnc-C17orf58-8:5 RNACentral:URS0000D5D119,RNACentral:URS00008C3464,RNACentral:URS0000D5AFEC,RNACentral:URS00009B5976,RNACentral:URS0000D579D0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:67692675..67692740 26863196 MeRIP-seq:(Medium) rs772217923 Functional Loss SNV dbSNP153 33..33 33 - - - 99130 RMVar_ID_99130 Human_SNP_ID_630835647 m1A Human chr17 + 67692735 67692735 67692735 CCTTCTAGTGCTCCATCCACCCCTCTCTCCACAGACGCACCCGAATTTCTGTCCGTTCCCAAAGA CCTTCTAGTGCTCCATCCACCCCTCTCTCCACCGACGCACCCGAATTTCTGTCCGTTCCCAAAGA A C PITPNC1 Ensembl:ENSG00000154217 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:67692685..67692789 26863196 MeRIP-seq:(Medium) rs543432687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126965,RMVar_hsa_circ_186674,RMVar_hsa_circ_111029,RMVar_hsa_circ_186678 99131 RMVar_ID_99131 Human_SNP_ID_630841929 m1A Human chr17 + 67717993 67717993 67717993 AGGAAGAATTCACGTTGTCTTCGGTAGTCCTGAGCGCCGGGCCTGAAGGACTCCTAGGCGTGGAG AGGAAGAATTCACGTTGTCTTCGGTAGTCCTGGGCGCCGGGCCTGAAGGACTCCTAGGCGTGGAG A G NOL11 Ensembl:ENSG00000130935 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:67717926..67718100 26863196 MeRIP-seq:(Medium) rs761580184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498032,Human_RBP_ID_1183870,Human_RBP_ID_1540780,Human_RBP_ID_1867929,Human_RBP_ID_4446960,Human_RBP_ID_8821708,Human_RBP_ID_9289336,Human_RBP_ID_13143455,Human_RBP_ID_22445712,Human_RBP_ID_26330853 Human_Splice_Rec_1857287,Human_Splice_Rec_1857297,Human_Splice_Rec_1857331,Human_Splice_Rec_1857337 RMVar_hsa_circ_21713 99132 RMVar_ID_99132 Human_SNP_ID_630845129 m1A Human chr17 + 67729411 67729411 67729411 AAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGCCAACGTCTTGTTTTAAAACATTTTCA AAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGGCCAACGTCTTGTTTTAAAACATTTTCA A G NOL11 Ensembl:ENSG00000130935 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:67729400..67729487 26863410 MeRIP-seq:(Medium) rs1484451053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328185,RMVar_hsa_circ_376197,RMVar_hsa_circ_88636,RMVar_hsa_circ_59347,RMVar_hsa_circ_186679,RMVar_hsa_circ_186680,RMVar_hsa_circ_186681,RMVar_hsa_circ_17581,RMVar_hsa_circ_109158,RMVar_hsa_circ_367455,RMVar_hsa_circ_186684 99133 RMVar_ID_99133 Human_SNP_ID_630869898 m1A Human chr17 - 67825616 67825616 67825616 GCCGGGTGGGGAGGCCCGCGGGGCCGGGCGGGAGGGGCCCGGCCGACGGAAGCGGGTGGAGGGAG GCCGGGTGGGGAGGCCCGCGGGGCCGGGCGGGGGGGGCCCGGCCGACGGAAGCGGGTGGAGGGAG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:67825526..67825725;chr17:67825526..67825700 26863410 MeRIP-seq:(Medium) rs989246931 Functional Loss SNV dbSNP153 33..33 33 - - - 99134 RMVar_ID_99134 Human_SNP_ID_630869920 m1A Human chr17 + 67825662 67825662 67825662 GCGGGCCTCCCCACCCGGCCCCGGCGCTCCCCACCGCCCCCCCTGCGCCCGCCCCTCCCCCTTCG GCGGGCCTCCCCACCCGGCCCCGGCGCTCCCCCCCGCCCCCCCTGCGCCCGCCCCTCCCCCTTCG A C BPTF Ensembl:ENSG00000171634 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:67825632..67825771 32194978 MeRIP-seq:(Medium) rs1242894118 Functional Loss SNV dbSNP153 33..33 33 - - - 99135 RMVar_ID_99135 Human_SNP_ID_630870160 m1A Human chr17 - 67826148 67826146 67826149 GGCGTCGCCGTCCTCCTCCTCCTCCTCCTCGGAGACCATGTCCTCCTCTTCCTCCTCCTCCTCGC GGCGTCGCCGTCCTCCTCCTCCTCCTCCTCG___ACCATGTCCTCCTCTTCCTCCTCCTCCTCGC TCTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:67825990..67826204 26863196 MeRIP-seq:(Medium) rs767192862 Functional Loss DEL dbSNP153 32..34 33 - - - 99136 RMVar_ID_99136 Human_SNP_ID_630870202 m1A Human chr17 + 67826220 67826220 67826220 CCCAGGATTCTGAGGACGACGAGGAGGATGAGATGGAAGAGGACGACGATGACTCCGATTATCCG CCCAGGATTCTGAGGACGACGAGGAGGATGAGGTGGAAGAGGACGACGATGACTCCGATTATCCG A G BPTF Ensembl:ENSG00000171634 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:67826108..67826255 32194978 MeRIP-seq:(Medium) rs1447361025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238132,Human_RBP_ID_768663,Human_RBP_ID_4447047,Human_RBP_ID_5577697,Human_RBP_ID_8253647,Human_RBP_ID_9289340,Human_RBP_ID_13144249,Human_RBP_ID_18412067,Human_RBP_ID_18530862,Human_RBP_ID_22063288,Human_RBP_ID_22740576,Human_RBP_ID_22959270,Human_RBP_ID_23118787,Human_RBP_ID_24371849,Human_RBP_ID_24545235,Human_RBP_ID_26330854,Human_RBP_ID_27456038,Human_RBP_ID_27814222 99137 RMVar_ID_99137 Human_SNP_ID_630900890 m1A Human chr17 - 67945527 67945527 67945527 TGGGTTTGGGGCTGGGGCTGAGCTGAAGGCTGAGCAGTCTGTGGCTGGGCTTCTGCTGGACCCAC TGGGTTTGGGGCTGGGGCTGAGCTGAAGGCTGCGCAGTCTGTGGCTGGGCTTCTGCTGGACCCAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:67945477..67945776 26863196 MeRIP-seq:(Medium) rs200425015 Functional Loss SNV dbSNP153 33..33 33 - - - 99138 RMVar_ID_99138 Human_SNP_ID_630904790 m1A Human chr17 - 67959642 67959642 67959642 GGTGAAGGTGGAGGGGCTGGAGGGGCTGGAGGAGCTGGTGTCACTGGGGGGCAGGGTGCAGCTAC GGTGAAGGTGGAGGGGCTGGAGGGGCTGGAGGGGCTGGTGTCACTGGGGGGCAGGGTGCAGCTAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:67959592..67959746 26863196 MeRIP-seq:(Medium) rs202116659 Functional Loss SNV dbSNP153 33..33 33 - - - 99139 RMVar_ID_99139 Human_SNP_ID_630914074 m1A Human chr17 + 67994025 67994025 67994025 AGAGAAGAGGAGAGGCGGGAAGGCGGTGGGGGAGGAGAAGCAGTGAGGGGAGGCCGTCGGGGAAA AGAGAAGAGGAGAGGCGGGAAGGCGGTGGGGGGGGAGAAGCAGTGAGGGGAGGCCGTCGGGGAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:67993974..67994269 26863196 MeRIP-seq:(Medium) rs1555699546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6639255 99140 RMVar_ID_99140 Human_SNP_ID_630914087 m1A Human chr17 - 67994097 67994097 67994097 TGGCTTCCCTTCCCCTCTCGGCCTCCCGTCTCAGCCTCCCCTTCCCTCTTCTTCCTTCTCGGCTT TGGCTTCCCTTCCCCTCTCGGCCTCCCGTCTCGGCCTCCCCTTCCCTCTTCTTCCTTCTCGGCTT T C C17orf58 Ensembl:ENSG00000186665 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:67993886..67994297 26863196 MeRIP-seq:(Medium) rs1465059752 Functional Loss SNV dbSNP153 33..33 33 - - - 99141 RMVar_ID_99141 Human_SNP_ID_630925961 m1A Human chr17 + 68035776 68035776 68035776 TTGAGCTGAGTCGAGGTGGACCCTTTGAACGCAGTCGCCCTACAGCCGCTGATTCCCCCCGCATC TTGAGCTGAGTCGAGGTGGACCCTTTGAACGCGGTCGCCCTACAGCCGCTGATTCCCCCCGCATC A G KPNA2 Ensembl:ENSG00000182481 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:68035751..68035775;chr17:68035726..68035987 26863196 MeRIP-seq:(Medium) rs1028313688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50927,Human_RBP_ID_498125,Human_RBP_ID_1541027,Human_RBP_ID_1868249,Human_RBP_ID_4447382,Human_RBP_ID_5441780,Human_RBP_ID_5497609,Human_RBP_ID_6639273,Human_RBP_ID_8461689,Human_RBP_ID_8821912,Human_RBP_ID_9289344,Human_RBP_ID_13146788,Human_RBP_ID_18707230,Human_RBP_ID_22219936,Human_RBP_ID_22444869,Human_RBP_ID_23746115,Human_RBP_ID_27258751 Human_Splice_Rec_1857839,Human_Splice_Rec_1857847,Human_Splice_Rec_1857855 99142 RMVar_ID_99142 Human_SNP_ID_630925970 m1A Human chr17 + 68035787 68035787 68035787 CGAGGTGGACCCTTTGAACGCAGTCGCCCTACAGCCGCTGATTCCCCCCGCATCGCCTCCCGTGG CGAGGTGGACCCTTTGAACGCAGTCGCCCTACCGCCGCTGATTCCCCCCGCATCGCCTCCCGTGG A C KPNA2 Ensembl:ENSG00000182481 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:68035726..68035956;chr17:68035726..68035850 26863196 MeRIP-seq:(Medium) rs909148374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50927,Human_RBP_ID_498125,Human_RBP_ID_1541027,Human_RBP_ID_1868249,Human_RBP_ID_4447383,Human_RBP_ID_5441780,Human_RBP_ID_5497609,Human_RBP_ID_6639273,Human_RBP_ID_8821912,Human_RBP_ID_9289344,Human_RBP_ID_13146789,Human_RBP_ID_18439566,Human_RBP_ID_18707233,Human_RBP_ID_22444869,Human_RBP_ID_22806427,Human_RBP_ID_23746115,Human_RBP_ID_26969724,Human_RBP_ID_27258751 Human_Splice_Rec_1857839,Human_Splice_Rec_1857847,Human_Splice_Rec_1857855 99143 RMVar_ID_99143 Human_SNP_ID_630925971 m1A Human chr17 + 68035787 68035787 68035787 CGAGGTGGACCCTTTGAACGCAGTCGCCCTACAGCCGCTGATTCCCCCCGCATCGCCTCCCGTGG CGAGGTGGACCCTTTGAACGCAGTCGCCCTACTGCCGCTGATTCCCCCCGCATCGCCTCCCGTGG A T KPNA2 Ensembl:ENSG00000182481 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:68035726..68035956;chr17:68035726..68035850 26863196 MeRIP-seq:(Medium) rs909148374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50927,Human_RBP_ID_498125,Human_RBP_ID_1541027,Human_RBP_ID_1868249,Human_RBP_ID_4447383,Human_RBP_ID_5441780,Human_RBP_ID_5497609,Human_RBP_ID_6639273,Human_RBP_ID_8821912,Human_RBP_ID_9289344,Human_RBP_ID_13146789,Human_RBP_ID_18439566,Human_RBP_ID_18707233,Human_RBP_ID_22444869,Human_RBP_ID_22806427,Human_RBP_ID_23746115,Human_RBP_ID_26969724,Human_RBP_ID_27258751 Human_Splice_Rec_1857839,Human_Splice_Rec_1857847,Human_Splice_Rec_1857855 99144 RMVar_ID_99144 Human_SNP_ID_630925975 m1A Human chr17 - 68035793 68035793 68035793 GGGCTTCCACGGGAGGCGATGCGGGGGGAATCAGCGGCTGTAGGGCGACTGCGTTCAAAGGGTCC GGGCTTCCACGGGAGGCGATGCGGGGGGAATCTGCGGCTGTAGGGCGACTGCGTTCAAAGGGTCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:68035726..68035987;chr17:68035701..68035987;chr17:68035726..68035907 26863196 MeRIP-seq:(Medium) rs1347124729 Functional Loss SNV dbSNP153 33..33 33 - - - 99145 RMVar_ID_99145 Human_SNP_ID_630926362 m1A Human chr17 + 68037162 68037162 68037162 ACCATGTCCACCAACGAGAATGCTAATACACCAGCTGCCCGTCTTCACAGATTCAAGAACAAGGG ACCATGTCCACCAACGAGAATGCTAATACACCCGCTGCCCGTCTTCACAGATTCAAGAACAAGGG A C KPNA2 Ensembl:ENSG00000182481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:68037062..68037382;chr17:68037101..68037200 26863196 MeRIP-seq:(Medium) rs145937092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49464,Human_RBP_ID_498128,Human_RBP_ID_766464,Human_RBP_ID_1010192,Human_RBP_ID_1541030,Human_RBP_ID_1868251,Human_RBP_ID_3535875,Human_RBP_ID_5497611,Human_RBP_ID_6639295,Human_RBP_ID_8461690,Human_RBP_ID_8821917,Human_RBP_ID_9075801,Human_RBP_ID_9376760,Human_RBP_ID_13146836,Human_RBP_ID_17261667,Human_RBP_ID_17493652,Human_RBP_ID_18707235,Human_RBP_ID_22806428,Human_RBP_ID_26969725 Human_Splice_Rec_1857840,Human_Splice_Rec_1857841,Human_Splice_Rec_1857848,Human_Splice_Rec_1857849,Human_Splice_Rec_1857856,Human_Splice_Rec_1857857,Human_Splice_Rec_1857876,Human_Splice_Rec_1857877,Human_Splice_Rec_1857895 Human_miRNA_ID_2052555,Human_miRNA_ID_2473485,Human_miRNA_ID_2710133 RMVar_hsa_circ_126653,RMVar_hsa_circ_112240,RMVar_hsa_circ_369444,RMVar_hsa_circ_375157,RMVar_hsa_circ_186765,RMVar_hsa_circ_373965,RMVar_hsa_circ_355067,RMVar_hsa_circ_186767,RMVar_hsa_circ_186769,RMVar_hsa_circ_72740,RMVar_hsa_circ_186768,RMVar_hsa_circ_186766 99146 RMVar_ID_99146 Human_SNP_ID_630926363 m1A Human chr17 + 68037162 68037162 68037162 ACCATGTCCACCAACGAGAATGCTAATACACCAGCTGCCCGTCTTCACAGATTCAAGAACAAGGG ACCATGTCCACCAACGAGAATGCTAATACACCGGCTGCCCGTCTTCACAGATTCAAGAACAAGGG A G KPNA2 Ensembl:ENSG00000182481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:68037062..68037382;chr17:68037101..68037200 26863196 MeRIP-seq:(Medium) rs145937092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49464,Human_RBP_ID_498128,Human_RBP_ID_766464,Human_RBP_ID_1010192,Human_RBP_ID_1541030,Human_RBP_ID_1868251,Human_RBP_ID_3535875,Human_RBP_ID_5497611,Human_RBP_ID_6639295,Human_RBP_ID_8461690,Human_RBP_ID_8821917,Human_RBP_ID_9075801,Human_RBP_ID_9376760,Human_RBP_ID_13146836,Human_RBP_ID_17261667,Human_RBP_ID_17493652,Human_RBP_ID_18707235,Human_RBP_ID_22806428,Human_RBP_ID_26969725 Human_Splice_Rec_1857840,Human_Splice_Rec_1857841,Human_Splice_Rec_1857848,Human_Splice_Rec_1857849,Human_Splice_Rec_1857856,Human_Splice_Rec_1857857,Human_Splice_Rec_1857876,Human_Splice_Rec_1857877,Human_Splice_Rec_1857895 Human_miRNA_ID_2052555,Human_miRNA_ID_2473485,Human_miRNA_ID_2710133 RMVar_hsa_circ_126653,RMVar_hsa_circ_112240,RMVar_hsa_circ_369444,RMVar_hsa_circ_375157,RMVar_hsa_circ_186765,RMVar_hsa_circ_373965,RMVar_hsa_circ_355067,RMVar_hsa_circ_186767,RMVar_hsa_circ_186769,RMVar_hsa_circ_72740,RMVar_hsa_circ_186768,RMVar_hsa_circ_186766 99147 RMVar_ID_99147 Human_SNP_ID_630928176 m1A Human chr17 + 68042990 68042990 68042990 CTGTTGGCTCTCCTTGCAGTTCCTGATATGTCATCTTTAGCAGTAAGTTACTAACATGAGTAAAG CTGTTGGCTCTCCTTGCAGTTCCTGATATGTCCTCTTTAGCAGTAAGTTACTAACATGAGTAAAG A C KPNA2 Ensembl:ENSG00000182481 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68042191..68042992 32194978 MeRIP-seq:(Medium) rs183768434 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_498134,Human_RBP_ID_1541051,Human_RBP_ID_1868267,Human_RBP_ID_3535892,Human_RBP_ID_8461704,Human_RBP_ID_22445721,Human_RBP_ID_22761668 Human_Splice_Rec_1857864,Human_Splice_Rec_1857865,Human_Splice_Rec_1857884,Human_Splice_Rec_1857885 RMVar_hsa_circ_11287,RMVar_hsa_circ_126653,RMVar_hsa_circ_112240,RMVar_hsa_circ_375157,RMVar_hsa_circ_186765,RMVar_hsa_circ_373965,RMVar_hsa_circ_186767,RMVar_hsa_circ_186769,RMVar_hsa_circ_72740,RMVar_hsa_circ_186768,RMVar_hsa_circ_125939,RMVar_hsa_circ_186772 99148 RMVar_ID_99148 Human_SNP_ID_630928553 m1A Human chr17 + 68043996 68043996 68043996 AAGGAAGCTACGTGGACAATGTCAAACATCACAGCCGGCCGCCAGGACCAGATACAGCAAGTTGT AAGGAAGCTACGTGGACAATGTCAAACATCACTGCCGGCCGCCAGGACCAGATACAGCAAGTTGT A T KPNA2 Ensembl:ENSG00000182481 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:68043855..68044044 26863196 MeRIP-seq:(Medium) rs782463222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498141,Human_RBP_ID_766469,Human_RBP_ID_903536,Human_RBP_ID_1010205,Human_RBP_ID_1541064,Human_RBP_ID_1868276,Human_RBP_ID_3535898,Human_RBP_ID_6639338,Human_RBP_ID_8461714,Human_RBP_ID_8821936,Human_RBP_ID_9376769,Human_RBP_ID_13146989,Human_RBP_ID_17261685,Human_RBP_ID_17377389,Human_RBP_ID_17493665,Human_RBP_ID_18470285,Human_RBP_ID_18707265,Human_RBP_ID_22806447,Human_RBP_ID_26969749,Human_RBP_ID_27456103 Human_Splice_Rec_1857869,Human_Splice_Rec_1857889 RMVar_hsa_circ_126653,RMVar_hsa_circ_112240,RMVar_hsa_circ_186765,RMVar_hsa_circ_373965,RMVar_hsa_circ_186769,RMVar_hsa_circ_72740,RMVar_hsa_circ_186768,RMVar_hsa_circ_26647,RMVar_hsa_circ_97486,RMVar_hsa_circ_186773 99149 RMVar_ID_99149 Human_SNP_ID_630955482 m1A Human chr17 - 68128691 68128691 68128691 GCTGTGATGGTAGTAAGAACACAGGCACACTGAGGATGAGGAGGGAGGCTTGTGCTCTCTCTGCA GCTGTGATGGTAGTAAGAACACAGGCACACTGGGGATGAGGAGGGAGGCTTGTGCTCTCTCTGCA T C LRRC37A16P Ensembl:ENSG00000267023 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68128546..68128844 32194978 MeRIP-seq:(Medium) rs1350118646 Functional Loss SNV dbSNP153 33..33 33 - - - 99150 RMVar_ID_99150 Human_SNP_ID_630955854 m1A Human chr17 - 68130398 68130398 68130398 CTCAGTAACACCTTTCTGCCCAGCCCTGTGGTAGCGTTGGCCTGCCTCCTTTGCCTACTCAAGTA CTCAGTAACACCTTTCTGCCCAGCCCTGTGGTTGCGTTGGCCTGCCTCCTTTGCCTACTCAAGTA T A LRRC37A16P Ensembl:ENSG00000267023 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:68130347..68130504 26863196 MeRIP-seq:(Medium) rs1467633149 Functional Loss SNV dbSNP153 33..33 33 - - - 99151 RMVar_ID_99151 Human_SNP_ID_630955858 m1A Human chr17 + 68130425 68130425 68130425 AACGCTACCACAGGGCTGGGCAGAAAGGTGTTACTGAGGCCTGTGGACTGGACAGTTGGGTAGGA AACGCTACCACAGGGCTGGGCAGAAAGGTGTTGCTGAGGCCTGTGGACTGGACAGTTGGGTAGGA A G LINC00674 RNACentral:URS000075B18A lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:68130375..68130469 26863196 MeRIP-seq:(Medium) rs147591624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6639560,Human_RBP_ID_13147723,Human_RBP_ID_23746207 99152 RMVar_ID_99152 Human_SNP_ID_630988827 m1A Human chr17 - 68248129 68248129 68248129 CTGCCTAGGGGCCCCGGCCCAGCTCTGACAGCACCCGCGAACCGCCCTGACCCGACAGGCCTCGA CTGCCTAGGGGCCCCGGCCCAGCTCTGACAGCGCCCGCGAACCGCCCTGACCCGACAGGCCTCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:68248051..68248615;chr17:68247970..68248350 26863196 MeRIP-seq:(Medium) rs1555736864 Functional Loss SNV dbSNP153 33..33 33 - - - 99153 RMVar_ID_99153 Human_SNP_ID_630999463 m1A Human chr17 - 68291570 68291570 68291570 GGGGCGGCCCGGCCCCGGACCGCGACGCGGTTACCTTTCGTGACCCCCAGCCCAGGCGGCAGGCT GGGGCGGCCCGGCCCCGGACCGCGACGCGGTTCCCTTTCGTGACCCCCAGCCCAGGCGGCAGGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:68291560..68291788 26863196 MeRIP-seq:(Medium) rs1555756034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8461790 99154 RMVar_ID_99154 Human_SNP_ID_631017357 m1A Human chr17 - 68363203 68363203 68363203 TCAGTTCTTAAGATCCAATTCCAAAGCCACCAATAGTCCTCCTCCTTTGCTCCCAGGTCATGGTT TCAGTTCTTAAGATCCAATTCCAAAGCCACCAGTAGTCCTCCTCCTTTGCTCCCAGGTCATGGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:68363152..68363373 26863196 MeRIP-seq:(Medium) rs1375772953 Functional Loss SNV dbSNP153 33..33 33 - - - 99155 RMVar_ID_99155 Human_SNP_ID_631031321 m1A Human chr17 - 68421634 68421634 68421634 AGGAATCCCGGGTGCTCCACTGCTTAAACCACAGGACCTGGTTAACTCCTCACCAAGCTTCCCAC AGGAATCCCGGGTGCTCCACTGCTTAAACCACGGGACCTGGTTAACTCCTCACCAAGCTTCCCAC T C WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68421583..68425936 32194978 MeRIP-seq:(Medium) rs900815906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2619361 RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 99156 RMVar_ID_99156 Human_SNP_ID_631038597 m1A Human chr17 - 68450897 68450897 68450897 CCATGTAACCTCCCGGCTGCTTTTCCTCCCAGATGAAATCCCGGACGTCTACATCGTGGAGCGCC CCATGTAACCTCCCGGCTGCTTTTCCTCCCAGTTGAAATCCCGGACGTCTACATCGTGGAGCGCC T A WIPI1 Ensembl:ENSG00000070540 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68450757..68452918 32194978 MeRIP-seq:(Medium) rs1400693349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1858280,Human_Splice_Rec_1858300,Human_Splice_Rec_1858324,Human_Splice_Rec_1858350,Human_Splice_Rec_1858394 Human_miRNA_ID_2378623,Human_miRNA_ID_3093693 RMVar_hsa_circ_2131,RMVar_hsa_circ_186795,RMVar_hsa_circ_350897,RMVar_hsa_circ_321544,RMVar_hsa_circ_323079,RMVar_hsa_circ_186801,RMVar_hsa_circ_307651,RMVar_hsa_circ_377048,RMVar_hsa_circ_186802,RMVar_hsa_circ_342175,RMVar_hsa_circ_36577,RMVar_hsa_circ_42660,RMVar_hsa_circ_186809,RMVar_hsa_circ_186807,RMVar_hsa_circ_332644,RMVar_hsa_circ_293075,RMVar_hsa_circ_112084,RMVar_hsa_circ_305200,RMVar_hsa_circ_186808 99157 RMVar_ID_99157 Human_SNP_ID_631053934 m1A Human chr17 + 68512498 68512498 68512498 GGGCTGGGAGCAAAGCGCTGAGGGAGCTCGGTACGCCGCCGCCTCGCACCCGCAGCCTCGCGCCC GGGCTGGGAGCAAAGCGCTGAGGGAGCTCGGTCCGCCGCCGCCTCGCACCCGCAGCCTCGCGCCC A C AC007780.1,PRKAR1A Ensembl:ENSG00000267009,Ensembl:ENSG00000108946 lincRNA,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr17:68512451..68512550;chr17:68512476..68512500 26863196,32194978 MeRIP-seq:(Medium) rs1258321700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820014,Human_RBP_ID_901566,Human_RBP_ID_3548445,Human_RBP_ID_4465633,Human_RBP_ID_5188625,Human_RBP_ID_5581502,Human_RBP_ID_5649273,Human_RBP_ID_8825706,Human_RBP_ID_9326803,Human_RBP_ID_22445731,Human_RBP_ID_22716615,Human_RBP_ID_23746316 Human_Splice_Rec_1858437,Human_Splice_Rec_1858457,Human_Splice_Rec_1858467,Human_Splice_Rec_1858479,Human_Splice_Rec_1858487,Human_Splice_Rec_1858507,Human_Splice_Rec_1858527,Human_Splice_Rec_1858549,Human_Splice_Rec_1858557 99158 RMVar_ID_99158 Human_SNP_ID_631054041 m1A Human chr17 + 68512742 68512742 68512742 CCTCACGCCCCCGGCTCCGAGTCTGCATCCTCAAGGCCGTCTGGGCGTTGGCTTTGGTGCGGGGC CCTCACGCCCCCGGCTCCGAGTCTGCATCCTCGAGGCCGTCTGGGCGTTGGCTTTGGTGCGGGGC A G AC007780.1,PRKAR1A Ensembl:ENSG00000267009,Ensembl:ENSG00000108946 lincRNA,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr17:68512738..68512950;chr17:68512740..68512905 26863196 MeRIP-seq:(Medium) rs1378549473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549263,Human_RBP_ID_4447690,Human_RBP_ID_5291232,Human_RBP_ID_5579658 99159 RMVar_ID_99159 Human_SNP_ID_631054051 m1A Human chr17 - 68512775 68512775 68512775 GGGGGCAGCGAGCGCGAGCGGGGCGGCTGGGGAGCCCCGCACCAAAGCCAACGCCCAGACGGCCT GGGGGCAGCGAGCGCGAGCGGGGCGGCTGGGGGGCCCCGCACCAAAGCCAACGCCCAGACGGCCT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:68512763..68512925 26863196 MeRIP-seq:(Medium) rs923647878 Functional Loss SNV dbSNP153 33..33 33 - - - 99160 RMVar_ID_99160 Human_SNP_ID_631054824 m1A Human chr17 + 68515333 68515333 68515333 GAATCAGTTGTCTAATGAATTTAGCAAGTTAAATGCCAGATTGACATTTTGCTTTATAGTTTATA GAATCAGTTGTCTAATGAATTTAGCAAGTTAAGTGCCAGATTGACATTTTGCTTTATAGTTTATA A G AC007780.1,PRKAR1A Ensembl:ENSG00000267009,Ensembl:ENSG00000108946 lincRNA,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:68515328..68515475 26863410 MeRIP-seq:(Medium) rs553498372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118332,RMVar_hsa_circ_361681,RMVar_hsa_circ_186810 99161 RMVar_ID_99161 Human_SNP_ID_631054851 m1A Human chr17 - 68515382 68515382 68515382 ACTGCCAGACTCCATGGTTCTCTGCGAGAAAAAAACACACACATGCTTGTATAAACTATAAAGCA ACTGCCAGACTCCATGGTTCTCTGCGAGAAAACAACACACACATGCTTGTATAAACTATAAAGCA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:68515376..68515425 26863196 MeRIP-seq:(Medium) rs905180467 Functional Loss SNV dbSNP153 33..33 33 - - - 99162 RMVar_ID_99162 Human_SNP_ID_631057632 m1A Human chr17 + 68525795 68525795 68525795 AACAATGAATGGGCAACCAGTGTTGGGGAAGGAGGGAGCTTTGGAGAACTTGCTTTGATTTATGG AACAATGAATGGGCAACCAGTGTTGGGGAAGGGGGGAGCTTTGGAGAACTTGCTTTGATTTATGG A G PRKAR1A Ensembl:ENSG00000108946 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68525757..68527629 32194978 MeRIP-seq:(Medium) rs991638429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50477,Human_RBP_ID_498364,Human_RBP_ID_768310,Human_RBP_ID_1010241,Human_RBP_ID_1868379,Human_RBP_ID_3536084,Human_RBP_ID_4467340,Human_RBP_ID_6639844,Human_RBP_ID_8091390,Human_RBP_ID_8461838,Human_RBP_ID_17899926,Human_RBP_ID_22445734,Human_RBP_ID_23746383 Human_Splice_Rec_1858416,Human_Splice_Rec_1858428,Human_Splice_Rec_1858448,Human_Splice_Rec_1858478,Human_Splice_Rec_1858498,Human_Splice_Rec_1858518,Human_Splice_Rec_1858540,Human_Splice_Rec_1858574,Human_Splice_Rec_1858598,Human_Splice_Rec_1858626 Human_miRNA_ID_895461,Human_miRNA_ID_902125,Human_miRNA_ID_908771,Human_miRNA_ID_915412,Human_miRNA_ID_950434,Human_miRNA_ID_1280285,Human_miRNA_ID_1540898,Human_miRNA_ID_1594477 Clinvar_Rec_609 RMVar_hsa_circ_68624,RMVar_hsa_circ_361681,RMVar_hsa_circ_325705,RMVar_hsa_circ_186811,RMVar_hsa_circ_60038,RMVar_hsa_circ_362020,RMVar_hsa_circ_58933,RMVar_hsa_circ_339114 99163 RMVar_ID_99163 Human_SNP_ID_631057641 m1A Human chr17 + 68525828 68525828 68525828 GGGAGCTTTGGAGAACTTGCTTTGATTTATGGAACACCGAGAGCAGCCACTGTCAAAGCAAAGAC GGGAGCTTTGGAGAACTTGCTTTGATTTATGGGACACCGAGAGCAGCCACTGTCAAAGCAAAGAC A G PRKAR1A Ensembl:ENSG00000108946 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:68525721..68525959 26863196 MeRIP-seq:(Medium) rs915785257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50477,Human_RBP_ID_1541170,Human_RBP_ID_1868379,Human_RBP_ID_6639848,Human_RBP_ID_13148349,Human_RBP_ID_18707382,Human_RBP_ID_22445734,Human_RBP_ID_24480816,Human_RBP_ID_26332324 Human_Splice_Rec_1858416,Human_Splice_Rec_1858428,Human_Splice_Rec_1858429,Human_Splice_Rec_1858448,Human_Splice_Rec_1858449,Human_Splice_Rec_1858478,Human_Splice_Rec_1858498,Human_Splice_Rec_1858499,Human_Splice_Rec_1858518,Human_Splice_Rec_1858519,Human_Splice_Rec_1858540,Human_Splice_Rec_1858541,Human_Splice_Rec_1858574,Human_Splice_Rec_1858575,Human_Splice_Rec_1858598,Human_Splice_Rec_1858599,Human_Splice_Rec_1858626,Human_Splice_Rec_1858627,Human_Splice_Rec_1858635,Human_Splice_Rec_1858641 RMVar_hsa_circ_68624,RMVar_hsa_circ_361681,RMVar_hsa_circ_325705,RMVar_hsa_circ_186811,RMVar_hsa_circ_60038,RMVar_hsa_circ_362020,RMVar_hsa_circ_58933,RMVar_hsa_circ_339114,RMVar_hsa_circ_186814 99164 RMVar_ID_99164 Human_SNP_ID_631057644 m1A Human chr17 + 68525837 68525837 68525837 GGAGAACTTGCTTTGATTTATGGAACACCGAGAGCAGCCACTGTCAAAGCAAAGACAAATGTGAA GGAGAACTTGCTTTGATTTATGGAACACCGAGGGCAGCCACTGTCAAAGCAAAGACAAATGTGAA A G PRKAR1A Ensembl:ENSG00000108946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:68525722..68525855 26863196 MeRIP-seq:(Medium) rs778368357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1868379,Human_RBP_ID_6639848,Human_RBP_ID_13148349,Human_RBP_ID_18707382,Human_RBP_ID_22445734,Human_RBP_ID_26332324 Human_Splice_Rec_1858416,Human_Splice_Rec_1858428,Human_Splice_Rec_1858429,Human_Splice_Rec_1858448,Human_Splice_Rec_1858449,Human_Splice_Rec_1858478,Human_Splice_Rec_1858498,Human_Splice_Rec_1858499,Human_Splice_Rec_1858518,Human_Splice_Rec_1858519,Human_Splice_Rec_1858540,Human_Splice_Rec_1858541,Human_Splice_Rec_1858574,Human_Splice_Rec_1858575,Human_Splice_Rec_1858598,Human_Splice_Rec_1858599,Human_Splice_Rec_1858626,Human_Splice_Rec_1858627,Human_Splice_Rec_1858635,Human_Splice_Rec_1858641 RMVar_hsa_circ_68624,RMVar_hsa_circ_361681,RMVar_hsa_circ_325705,RMVar_hsa_circ_186811,RMVar_hsa_circ_60038,RMVar_hsa_circ_362020,RMVar_hsa_circ_58933,RMVar_hsa_circ_339114,RMVar_hsa_circ_186814 99165 RMVar_ID_99165 Human_SNP_ID_631242620 m1A Human chr17 + 69282336 69282336 69282336 CTCCACTGCTCACCCAGGAGGCTTGCCCCTCAATTCTTATCTACACTCCTTACCCAACTAAGAGA CTCCACTGCTCACCCAGGAGGCTTGCCCCTCAGTTCTTATCTACACTCCTTACCCAACTAAGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:69282242..69282343 26863196 MeRIP-seq:(Medium) rs1465582994 Functional Loss SNV dbSNP153 33..33 33 - - - 99166 RMVar_ID_99166 Human_SNP_ID_631337314 m1A Human chr17 - 69675815 69675815 69675815 TACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCGGAGCTTGCAGTGAGCTGAGA TACTTGGGAGGCTGAGGCAGGAGAATGGCATGTACCCGGGAGGCGGAGCTTGCAGTGAGCTGAGA T A lnc-ABCA5-9 RNACentral:URS00008BF203 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:69675809..69675891 26863410 MeRIP-seq:(Medium) rs1266484374 Functional Loss SNV dbSNP153 33..33 33 - - - 99167 RMVar_ID_99167 Human_SNP_ID_631957264 m1A Human chr17 + 72122822 72122822 72122822 ACCACCCGGATTACAAGTACCAGCCGCGGCGGAGGAAGTCGGTGAAGAACGGGCAGGCGGAGGCA ACCACCCGGATTACAAGTACCAGCCGCGGCGGGGGAAGTCGGTGAAGAACGGGCAGGCGGAGGCA A G SOX9 Ensembl:ENSG00000125398 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:72122772..72122877 26863196 MeRIP-seq:(Medium) rs794727247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765083,Human_RBP_ID_901983,Human_RBP_ID_9376778,Human_RBP_ID_22443856 RMVar_hsa_circ_186856,RMVar_hsa_circ_115297 99168 RMVar_ID_99168 Human_SNP_ID_631957751 m1A Human chr17 + 72123927 72123918 72123927 GCAGCAGCCCCCACAGGCCCCGCCGGCCCCGCAGGCGCCCCCGCAGCCGCAGGCGGCGCCCCCAC GCAGCAGCCCCCACAGGCCCCGCC_________GGCGCCCCCGCAGCCGCAGGCGGCGCCCCCAC CGGCCCCGCA C SOX9 Ensembl:ENSG00000125398 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:72123830..72124080 26863410 MeRIP-seq:(Medium) rs1053830620 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_22444892 RMVar_hsa_circ_186856,RMVar_hsa_circ_115297 99169 RMVar_ID_99169 Human_SNP_ID_631957763 m1A Human chr17 + 72123927 72123927 72123927 GCAGCAGCCCCCACAGGCCCCGCCGGCCCCGCAGGCGCCCCCGCAGCCGCAGGCGGCGCCCCCAC GCAGCAGCCCCCACAGGCCCCGCCGGCCCCGCTGGCGCCCCCGCAGCCGCAGGCGGCGCCCCCAC A T SOX9 Ensembl:ENSG00000125398 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:72123830..72124080 26863410 MeRIP-seq:(Medium) rs527344892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444892 RMVar_hsa_circ_186856,RMVar_hsa_circ_115297 99170 RMVar_ID_99170 Human_SNP_ID_631957897 m1A Human chr17 + 72124160 72124160 72124160 ACCTCCCACACTACAGCCCCTCCTACCCGCCCATCACCCGCTCACAGTACGACTACACCGACCAC ACCTCCCACACTACAGCCCCTCCTACCCGCCCGTCACCCGCTCACAGTACGACTACACCGACCAC A G SOX9 Ensembl:ENSG00000125398 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:72124118..72124264 26863196 MeRIP-seq:(Medium) rs202126529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765086,Human_RBP_ID_17263653,Human_RBP_ID_17495009,Human_RBP_ID_18942028 Human_miRNA_ID_2673340 RMVar_hsa_circ_186856,RMVar_hsa_circ_115297 99171 RMVar_ID_99171 Human_SNP_ID_632161572 m1A Human chr17 - 72920879 72920879 72920879 CAGATAAGGGGGTAAGACGTATGCATGTGTGTATGGGGTGTAGATGTTGTAGAGGGGGTGGGAAG CAGATAAGGGGGTAAGACGTATGCATGTGTGTGTGGGGTGTAGATGTTGTAGAGGGGGTGGGAAG T C SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:72920874..72920959 26863196 MeRIP-seq:(Medium) rs1262505088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_110240,RMVar_hsa_circ_343678,RMVar_hsa_circ_186867 99172 RMVar_ID_99172 Human_SNP_ID_632182504 m1A Human chr17 - 73000282 73000280 73000282 GATTGAGAGAGAGAGAGAGAAGGCAGAGAGAGAGGGGAGAAAGGAGAGATGAGAGGAGAGGGAGA GATTGAGAGAGAGAGAGAGAAGGCAGAGAGAG__GGGAGAAAGGAGAGATGAGAGGAGAGGGAGA CCT C SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73000280..73000345 26863196 MeRIP-seq:(Medium) rs1218115447 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110240,RMVar_hsa_circ_186867,RMVar_hsa_circ_62613,RMVar_hsa_circ_266456 99173 RMVar_ID_99173 Human_SNP_ID_632205777 m1A Human chr17 - 73088764 73088764 73088764 CCTCTCGCTCCTCTTGCACAGCTGTATCCAGCATGCTCCAAGGCCACAGCTCTGTGTTCCAGGCC CCTCTCGCTCCTCTTGCACAGCTGTATCCAGCTTGCTCCAAGGCCACAGCTCTGTGTTCCAGGCC T A SLC39A11 Ensembl:ENSG00000133195 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:73088713..73088791 26863196 MeRIP-seq:(Medium) rs759960768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4448295,Human_RBP_ID_18989071 Human_Splice_Rec_1861658,Human_Splice_Rec_1861676,Human_Splice_Rec_1861728,Human_Splice_Rec_1861740,Human_Splice_Rec_1861750,Human_Splice_Rec_1861758,Human_Splice_Rec_1861764,Human_Splice_Rec_1861774,Human_Splice_Rec_1861780 RMVar_hsa_circ_186869,RMVar_hsa_circ_99885 99174 RMVar_ID_99174 Human_SNP_ID_632205778 m1A Human chr17 - 73088764 73088764 73088764 CCTCTCGCTCCTCTTGCACAGCTGTATCCAGCATGCTCCAAGGCCACAGCTCTGTGTTCCAGGCC CCTCTCGCTCCTCTTGCACAGCTGTATCCAGCGTGCTCCAAGGCCACAGCTCTGTGTTCCAGGCC T C SLC39A11 Ensembl:ENSG00000133195 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:73088713..73088791 26863196 MeRIP-seq:(Medium) rs759960768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4448295,Human_RBP_ID_18989071 Human_Splice_Rec_1861658,Human_Splice_Rec_1861676,Human_Splice_Rec_1861728,Human_Splice_Rec_1861740,Human_Splice_Rec_1861750,Human_Splice_Rec_1861758,Human_Splice_Rec_1861764,Human_Splice_Rec_1861774,Human_Splice_Rec_1861780 RMVar_hsa_circ_186869,RMVar_hsa_circ_99885 99175 RMVar_ID_99175 Human_SNP_ID_632206804 m1A Human chr17 - 73092666 73092666 73092666 AGCAGGAAGTGACTGCGGGAGTGGAGCCGGCGAGAGAGTGGCAGCGGGGGCTGATGGAAGTGCAG AGCAGGAAGTGACTGCGGGAGTGGAGCCGGCGGGAGAGTGGCAGCGGGGGCTGATGGAAGTGCAG T C SLC39A11 Ensembl:ENSG00000133195 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:73092543..73092694 26863196 MeRIP-seq:(Medium) rs995999808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4448299,Human_RBP_ID_18992075,Human_RBP_ID_27814257 Human_Splice_Rec_1861657,Human_Splice_Rec_1861675,Human_Splice_Rec_1861727,Human_Splice_Rec_1861757,Human_Splice_Rec_1861763,Human_Splice_Rec_1861771,Human_Splice_Rec_1861781 RMVar_hsa_circ_186869,RMVar_hsa_circ_99885 99176 RMVar_ID_99176 Human_SNP_ID_632234225 m1A Human chr17 + 73192743 73192743 73192743 AGGGAAAGGGAAGACTTCAGCCACAGTTTCGCAGCCAACCTGGCGACCTCACCTCTCTGGCGACC AGGGAAAGGGAAGACTTCAGCCACAGTTTCGCTGCCAACCTGGCGACCTCACCTCTCTGGCGACC A T COG1,AC097641.1 Ensembl:ENSG00000166685,Ensembl:ENSG00000264860 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:73192595..73192772;chr17:73192611..73192781 26863196 MeRIP-seq:(Medium) rs1297522493 Functional Loss SNV dbSNP153 33..33 33 - - - 99177 RMVar_ID_99177 Human_SNP_ID_632234576 m1A Human chr17 + 73193119 73193119 73193119 CTCACCCGCGCTGAAGCGGCTGGATCTGCGCGACCCTGCGGCTCTTTTCGAGACGCATGGAGCGG CTCACCCGCGCTGAAGCGGCTGGATCTGCGCGCCCCTGCGGCTCTTTTCGAGACGCATGGAGCGG A C COG1,AC097641.1 Ensembl:ENSG00000166685,Ensembl:ENSG00000264860 Protein coding,lincRNA CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:73193071..73193181 26863196 MeRIP-seq:(Medium) rs1381566085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466743,Human_RBP_ID_5582148 99178 RMVar_ID_99178 Human_SNP_ID_632237474 m1A Human chr17 + 73203050 73203050 73203050 ACCCAGTCATTACTTCTAGATGATGCTGGCTCAGTTCTGGCCACAGCCACCAGCTGGGATGAGCT ACCCAGTCATTACTTCTAGATGATGCTGGCTCTGTTCTGGCCACAGCCACCAGCTGGGATGAGCT A T COG1 Ensembl:ENSG00000166685 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:73201856..73203153 32194978 MeRIP-seq:(Medium) rs889560403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5364738,Human_RBP_ID_18989073,Human_RBP_ID_27813094 Human_Splice_Rec_1861808,Human_Splice_Rec_1861809,Human_Splice_Rec_1861836,Human_Splice_Rec_1861837,Human_Splice_Rec_1861862,Human_Splice_Rec_1861863 Human_miRNA_ID_272311,Human_miRNA_ID_1810569,Human_miRNA_ID_2052558 RMVar_hsa_circ_92958,RMVar_hsa_circ_47927,RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_186871,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_312560,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833,RMVar_hsa_circ_308613,RMVar_hsa_circ_186876 99179 RMVar_ID_99179 Human_SNP_ID_632245691 m1A Human chr17 + 73231963 73231963 73231963 GCGCATCCCTCTCCCCTCCTCCCCCGGCCCGCAGTGCACCCCACAGGGAGCCCCGCCGGGTCCAC GCGCATCCCTCTCCCCTCCTCCCCCGGCCCGCGGTGCACCCCACAGGGAGCCCCGCCGGGTCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:73231957..73232050 26863196 MeRIP-seq:(Medium) rs560333675 Functional Loss SNV dbSNP153 33..33 33 - - - 99180 RMVar_ID_99180 Human_SNP_ID_632245759 m1A Human chr17 - 73232142 73232142 73232142 AACACAACCCCCTCTGTTCCCTCTCTTCGCGGAGCGGCGCCGCGTAGCTTCCATCCGCCAGCTGC AACACAACCCCCTCTGTTCCCTCTCTTCGCGGCGCGGCGCCGCGTAGCTTCCATCCGCCAGCTGC T G FAM104A Ensembl:ENSG00000133193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:73232046..73232297 26863196 MeRIP-seq:(Medium) rs754844655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1861905,Human_Splice_Rec_1861909,Human_Splice_Rec_1861925,Human_Splice_Rec_1861933 99181 RMVar_ID_99181 Human_SNP_ID_632245803 m1A Human chr17 + 73232217 73232217 73232217 CCACGCCCACCCCCTCGGGCCTTGGCTCTCGCAGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTA CCACGCCCACCCCCTCGGGCCTTGGCTCTCGCGGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73232048..73232339 26863196 MeRIP-seq:(Medium) rs780448847 Functional Loss SNV dbSNP153 33..33 33 - - - 99182 RMVar_ID_99182 Human_SNP_ID_632245835 m1A Human chr17 + 73232249 73232249 73232249 AGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTACCCCTCAGTCGGACCCGTACCACCACTACTTC AGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTGCCCCTCAGTCGGACCCGTACCACCACTACTTC A G C17orf80 Ensembl:ENSG00000141219 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:73232115..73232314 26863196 MeRIP-seq:(Medium) rs371082623 Functional Loss SNV dbSNP153 33..33 33 - - - 99183 RMVar_ID_99183 Human_SNP_ID_632247770 m1A Human chr17 + 73237831 73237831 73237831 TGGTAGGACACAGGTAAAACTAGCCAGGTAAGACGGGCAGGCAAGGCAGATAAGTGGAAGTGGAG TGGTAGGACACAGGTAAAACTAGCCAGGTAAGGCGGGCAGGCAAGGCAGATAAGTGGAAGTGGAG A G C17orf80 Ensembl:ENSG00000141219 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73237780..73237905 26863196 MeRIP-seq:(Medium) rs75834765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236297 RMVar_hsa_circ_186879,RMVar_hsa_circ_378151,RMVar_hsa_circ_186881,RMVar_hsa_circ_276349 99184 RMVar_ID_99184 Human_SNP_ID_632256121 m1A Human chr17 + 73269149 73269149 73269149 GCTCATTCACTCACTTGTTCACTCATTCACTCACTCATTCACCCATTCACTCACTCATTCACTCA GCTCATTCACTCACTTGTTCACTCATTCACTCGCTCATTCACCCATTCACTCACTCATTCACTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:73269107..73269190 26863196 MeRIP-seq:(Medium) rs934750730 Functional Loss SNV dbSNP153 33..33 33 - - - 99185 RMVar_ID_99185 Human_SNP_ID_632260823 m1A Human chr17 - 73286022 73286022 73286022 CGGGGAGGGCGGCGATGAGGAGGCGGGCACGGAGGAGGCAGTGCCCCGTCGGAATGGGGCCGCGG CGGGGAGGGCGGCGATGAGGAGGCGGGCACGGCGGAGGCAGTGCCCCGTCGGAATGGGGCCGCGG T G CDC42EP4 Ensembl:ENSG00000179604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73285897..73286039 26863196 MeRIP-seq:(Medium) rs1273012365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24371862 99186 RMVar_ID_99186 Human_SNP_ID_632261022 m1A Human chr17 - 73286444 73286444 73286444 TCCAGCTCGGTGCACTCCAAGCGCCGTTCCCGAGCGGACCTCACGGCCGAGATGATCAGCGCCCC TCCAGCTCGGTGCACTCCAAGCGCCGTTCCCGGGCGGACCTCACGGCCGAGATGATCAGCGCCCC T C CDC42EP4 Ensembl:ENSG00000179604 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:73286395..73286625 26863196 MeRIP-seq:(Medium) rs569802841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5466912 Human_Splice_Rec_1862029,Human_Splice_Rec_1862031 99187 RMVar_ID_99187 Human_SNP_ID_632261023 m1A Human chr17 - 73286444 73286444 73286444 TCCAGCTCGGTGCACTCCAAGCGCCGTTCCCGAGCGGACCTCACGGCCGAGATGATCAGCGCCCC TCCAGCTCGGTGCACTCCAAGCGCCGTTCCCGCGCGGACCTCACGGCCGAGATGATCAGCGCCCC T G CDC42EP4 Ensembl:ENSG00000179604 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:73286395..73286625 26863196 MeRIP-seq:(Medium) rs569802841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5466912 Human_Splice_Rec_1862029,Human_Splice_Rec_1862031 99188 RMVar_ID_99188 Human_SNP_ID_632268068 m1A Human chr17 + 73310991 73310991 73310991 GGGGGCGCTCCGGAGAGGGGGCGGGGCCAGGGACGGCCGATCCGCGCGCACCCGCCCCAAGCGGG GGGGGCGCTCCGGAGAGGGGGCGGGGCCAGGGCCGGCCGATCCGCGCGCACCCGCCCCAAGCGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73310986..73311068 26863196 MeRIP-seq:(Medium) rs1312081495 Functional Loss SNV dbSNP153 33..33 33 - - - 99189 RMVar_ID_99189 Human_SNP_ID_632503464 m1A Human chr17 + 74204179 74204179 74204179 AATCAAGGACTTCCTGCTCACAGCCCGACGAAAGGATGCCAAATGTAAGTGGTTGCTCCGAAGGT AATCAAGGACTTCCTGCTCACAGCCCGACGAAGGGATGCCAAATGTAAGTGGTTGCTCCGAAGGT A G RPL38 Ensembl:ENSG00000172809 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:74204079..74204245 26863196 MeRIP-seq:(Medium) rs770849321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236739,Human_RBP_ID_499073,Human_RBP_ID_766141,Human_RBP_ID_820508,Human_RBP_ID_902129,Human_RBP_ID_1541505,Human_RBP_ID_1868728,Human_RBP_ID_3536760,Human_RBP_ID_4449245,Human_RBP_ID_6641988,Human_RBP_ID_8462466,Human_RBP_ID_8822054,Human_RBP_ID_9376786,Human_RBP_ID_13155132,Human_RBP_ID_17495016,Human_RBP_ID_17654877,Human_RBP_ID_18708031,Human_RBP_ID_23748079,Human_RBP_ID_26813966,Human_RBP_ID_27456531 Human_Splice_Rec_1862446,Human_Splice_Rec_1862447,Human_Splice_Rec_1862456,Human_Splice_Rec_1862460,Human_Splice_Rec_1862461,Human_Splice_Rec_1862468,Human_Splice_Rec_1862469,Human_Splice_Rec_1862476,Human_Splice_Rec_1862477,Human_Splice_Rec_1862482,Human_Splice_Rec_1862484,Human_Splice_Rec_1862485 RMVar_hsa_circ_186904,RMVar_hsa_circ_78684,RMVar_hsa_circ_186901,RMVar_hsa_circ_106441,RMVar_hsa_circ_125225,RMVar_hsa_circ_97877,RMVar_hsa_circ_186902,RMVar_hsa_circ_186903,RMVar_hsa_circ_120834,RMVar_hsa_circ_186905 99190 RMVar_ID_99190 Human_SNP_ID_632505076 m1A Human chr17 + 74209237 74209237 74209237 ATAAGGACAACGTGAAGTTTAAAGTTCGATGCAGCAGATACCTTTACACCCTGGTCATCACTGAC ATAAGGACAACGTGAAGTTTAAAGTTCGATGCGGCAGATACCTTTACACCCTGGTCATCACTGAC A G RPL38 Ensembl:ENSG00000172809 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74209144..74209256 26863196 MeRIP-seq:(Medium) rs1399242429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499078,Human_RBP_ID_902131,Human_RBP_ID_1010350,Human_RBP_ID_1091155,Human_RBP_ID_1541514,Human_RBP_ID_1868736,Human_RBP_ID_2522246,Human_RBP_ID_3536766,Human_RBP_ID_4449251,Human_RBP_ID_5497717,Human_RBP_ID_6642044,Human_RBP_ID_8462478,Human_RBP_ID_9076119,Human_RBP_ID_13155361,Human_RBP_ID_17261835,Human_RBP_ID_17377518,Human_RBP_ID_17495018,Human_RBP_ID_17654878,Human_RBP_ID_18207921,Human_RBP_ID_18708036,Human_RBP_ID_22220546,Human_RBP_ID_22806572,Human_RBP_ID_23748107,Human_RBP_ID_26454981,Human_RBP_ID_26813967,Human_RBP_ID_26970500,Human_RBP_ID_27259224,Human_RBP_ID_27456532 Human_Splice_Rec_1862448,Human_Splice_Rec_1862449,Human_Splice_Rec_1862462,Human_Splice_Rec_1862463,Human_Splice_Rec_1862470,Human_Splice_Rec_1862471,Human_Splice_Rec_1862478,Human_Splice_Rec_1862486,Human_Splice_Rec_1862487 RMVar_hsa_circ_186904,RMVar_hsa_circ_186901,RMVar_hsa_circ_106441,RMVar_hsa_circ_125225,RMVar_hsa_circ_97877,RMVar_hsa_circ_186903,RMVar_hsa_circ_120834,RMVar_hsa_circ_186905,RMVar_hsa_circ_119162,RMVar_hsa_circ_186906 99191 RMVar_ID_99191 Human_SNP_ID_632505448 m1A Human chr17 + 74210367 74210367 74210367 AAATAGCACGTGGGGTTAAACATAACTGGCAGATGTGGGAGCGATGGTGGGGCATGCCATTCAAA AAATAGCACGTGGGGTTAAACATAACTGGCAGGTGTGGGAGCGATGGTGGGGCATGCCATTCAAA A G RPL38 Ensembl:ENSG00000172809 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74210326..74210463 26863196 MeRIP-seq:(Medium) rs752021453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499103,Human_RBP_ID_1010357,Human_RBP_ID_2528628,Human_RBP_ID_6642064,Human_RBP_ID_13155441,Human_RBP_ID_17900403,Human_RBP_ID_27669388 99192 RMVar_ID_99192 Human_SNP_ID_632565643 m1A Human chr17 + 74431509 74431509 74431509 CGGAGCAGGGAACGGGGACGCCGGGAGGGGAGAGCGCGCTCCGAGTTGGGCAGAACCTGGAACGG CGGAGCAGGGAACGGGGACGCCGGGAGGGGAGGGCGCGCTCCGAGTTGGGCAGAACCTGGAACGG A G GPRC5C Ensembl:ENSG00000170412 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74431400..74431724 26863196 MeRIP-seq:(Medium) rs1318716929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767377,Human_RBP_ID_4464756,Human_RBP_ID_5525836 99193 RMVar_ID_99193 Human_SNP_ID_632570329 m1A Human chr17 - 74447000 74447000 74447000 TGACTCAGTCCCACACGTAGGGGTTTCTAAAGACCTGAGAGTTCTTGCCGTCTTTCGGCGGTGTG TGACTCAGTCCCACACGTAGGGGTTTCTAAAGTCCTGAGAGTTCTTGCCGTCTTTCGGCGGTGTG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:74446949..74447298 32194978 MeRIP-seq:(Medium) rs1440222669 Functional Loss SNV dbSNP153 33..33 33 - - - 99194 RMVar_ID_99194 Human_SNP_ID_632651647 m1A Human chr17 - 74748672 74748672 74748672 CCAGGAACCGTCGGCCGCCGCGAGCCGCGAGGAGCCGAGAGAGGACCACAGACCAATCCCCGCCC CCAGGAACCGTCGGCCGCCGCGAGCCGCGAGGGGCCGAGAGAGGACCACAGACCAATCCCCGCCC T C AC016888.1 Ensembl:ENSG00000266036 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:74748626..74748850;chr17:74748651..74748725 26863196 MeRIP-seq:(Medium) rs1048939419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1863367 99195 RMVar_ID_99195 Human_SNP_ID_632651837 m1A Human chr17 - 74749031 74749031 74749031 GGTGGGTCTCCTTCTCCACGTTTTCGCCGTTCACCTCCACCAGCCGGTCCCCCGCCAGCAGCCCC GGTGGGTCTCCTTCTCCACGTTTTCGCCGTTCCCCTCCACCAGCCGGTCCCCCGCCAGCAGCCCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:74748723..74762155 32194978 MeRIP-seq:(Medium) rs777700723 Functional Loss SNV dbSNP153 33..33 33 - - - 99196 RMVar_ID_99196 Human_SNP_ID_632655200 m1A Human chr17 - 74762169 74762169 74762169 CAGATAGGAAGAGAGCGAGAAGCATCACCTCCACAATGCGATCCTGGGCCCGGAGCCCTGAAGCC CAGATAGGAAGAGAGCGAGAAGCATCACCTCCGCAATGCGATCCTGGGCCCGGAGCCCTGAAGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:74761962..74762227 26863196 MeRIP-seq:(Medium) rs765322250 Functional Loss SNV dbSNP153 33..33 33 - - - 99197 RMVar_ID_99197 Human_SNP_ID_632655549 m1A Human chr17 + 74763437 74763436 74763437 CGTGGTGTCCGCCATCAGGGCTGGCGGGGACGAGACCAAGCTGCTGGTGGTGGACAGGGAAACTG CGTGGTGTCCGCCATCAGGGCTGGCGGGGACG_GACCAAGCTGCTGGTGGTGGACAGGGAAACTG GA G SLC9A3R1 Ensembl:ENSG00000109062 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:74763322..74763833 26863196 MeRIP-seq:(Medium) rs769364805 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5367715,Human_RBP_ID_9353447,Human_RBP_ID_22443886 Human_Splice_Rec_1863372,Human_Splice_Rec_1863373,Human_Splice_Rec_1863384,Human_Splice_Rec_1863385,Human_Splice_Rec_1863391,Human_Splice_Rec_1863397 RMVar_hsa_circ_100590,RMVar_hsa_circ_110648,RMVar_hsa_circ_186921,RMVar_hsa_circ_83833,RMVar_hsa_circ_186920,RMVar_hsa_circ_308061,RMVar_hsa_circ_186922,RMVar_hsa_circ_186923 99198 RMVar_ID_99198 Human_SNP_ID_632655559 m1A Human chr17 + 74763458 74763458 74763458 TGGCGGGGACGAGACCAAGCTGCTGGTGGTGGACAGGGAAACTGACGAGTTCTTCAAGAAATGCA TGGCGGGGACGAGACCAAGCTGCTGGTGGTGGTCAGGGAAACTGACGAGTTCTTCAAGAAATGCA A T SLC9A3R1 Ensembl:ENSG00000109062 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:74763351..74763525 26863196 MeRIP-seq:(Medium) rs774771671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9353447 Human_Splice_Rec_1863372,Human_Splice_Rec_1863373,Human_Splice_Rec_1863384,Human_Splice_Rec_1863385,Human_Splice_Rec_1863391,Human_Splice_Rec_1863397 Human_miRNA_ID_642262,Human_miRNA_ID_976112,Human_miRNA_ID_2245820,Human_miRNA_ID_2444486 RMVar_hsa_circ_100590,RMVar_hsa_circ_110648,RMVar_hsa_circ_186921,RMVar_hsa_circ_83833,RMVar_hsa_circ_186920,RMVar_hsa_circ_308061,RMVar_hsa_circ_186922,RMVar_hsa_circ_186923 99199 RMVar_ID_99199 Human_SNP_ID_632656876 m1A Human chr17 - 74768216 74768216 74768216 TGGCTGGCCTACCTCCTCGCTGGTGTCACTGGAGGCGGATCTCACCAGGGCTGGCCTGGGGCTCT TGGCTGGCCTACCTCCTCGCTGGTGTCACTGGGGGCGGATCTCACCAGGGCTGGCCTGGGGCTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr17:74768126..74768250;chr17:74763404..74768236 26863196,32194978 MeRIP-seq:(Medium) rs1428891804 Functional Loss SNV dbSNP153 33..33 33 - - - 99200 RMVar_ID_99200 Human_SNP_ID_632656879 m1A Human chr17 + 74768225 74768225 74768225 GGCCAGCCCTGGTGAGATCCGCCTCCAGTGACACCAGCGAGGAGGTAGGCCAGCCATGCGGGGGG GGCCAGCCCTGGTGAGATCCGCCTCCAGTGACGCCAGCGAGGAGGTAGGCCAGCCATGCGGGGGG A G SLC9A3R1 Ensembl:ENSG00000109062 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:74768201..74768225 26863196 MeRIP-seq:(Medium) rs1020242568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18992084,Human_RBP_ID_22444919 Human_Splice_Rec_1863376,Human_Splice_Rec_1863377,Human_Splice_Rec_1863380,Human_Splice_Rec_1863381,Human_Splice_Rec_1863388,Human_Splice_Rec_1863389,Human_Splice_Rec_1863394,Human_Splice_Rec_1863395,Human_Splice_Rec_1863398,Human_Splice_Rec_1863399 Human_miRNA_ID_2052560 RMVar_hsa_circ_100590,RMVar_hsa_circ_120590,RMVar_hsa_circ_110648,RMVar_hsa_circ_186921,RMVar_hsa_circ_83833,RMVar_hsa_circ_186920,RMVar_hsa_circ_186923,RMVar_hsa_circ_186924 99201 RMVar_ID_99201 Human_SNP_ID_632657000 m1A Human chr17 - 74768518 74768518 74768518 TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTAGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTGGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:74768448..74768702;chr17:74768451..74768600;chr17:74768451..74768550 26863196 MeRIP-seq:(Medium) rs1567826348 Functional Loss SNV dbSNP153 33..33 33 - - - 99202 RMVar_ID_99202 Human_SNP_ID_632657001 m1A Human chr17 - 74768518 74768518 74768518 TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTAGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTCGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:74768448..74768702;chr17:74768451..74768600;chr17:74768451..74768550 26863196 MeRIP-seq:(Medium) rs1567826348 Functional Loss SNV dbSNP153 33..33 33 - - - 99203 RMVar_ID_99203 Human_SNP_ID_632657051 m1A Human chr17 + 74768600 74768600 74768600 CCAAAGAGAGGGCCCACCAGAAACGCAGCAGCAAACGGGCCCCGCAGATGGACTGGAGCAAGAAA CCAAAGAGAGGGCCCACCAGAAACGCAGCAGCTAACGGGCCCCGCAGATGGACTGGAGCAAGAAA A T SLC9A3R1 Ensembl:ENSG00000109062 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:74768551..74768875 26863196 MeRIP-seq:(Medium) rs957974780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27259254 Human_miRNA_ID_3066273 RMVar_hsa_circ_100590,RMVar_hsa_circ_120590,RMVar_hsa_circ_186920,RMVar_hsa_circ_186924 99204 RMVar_ID_99204 Human_SNP_ID_632657112 m1A Human chr17 + 74768726 74768726 74768726 CAGCATTCCACCCCACCTTTTTCCTTCTCCCCAATTACTCCCCTGAATCAATGTACAAATCAGCA CAGCATTCCACCCCACCTTTTTCCTTCTCCCCCATTACTCCCCTGAATCAATGTACAAATCAGCA A C SLC9A3R1 Ensembl:ENSG00000109062 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:74768451..74768800 26863196 MeRIP-seq:(Medium) rs1430832112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47634,Human_RBP_ID_499158,Human_RBP_ID_17654310,Human_RBP_ID_18942079,Human_RBP_ID_20172884,Human_RBP_ID_21890289,Human_RBP_ID_23748283,Human_RBP_ID_24415977,Human_RBP_ID_24481001,Human_RBP_ID_27259256,Human_RBP_ID_27456565,Human_RBP_ID_27561371 Human_miRNA_ID_842877,Human_miRNA_ID_2368096,Human_miRNA_ID_2766035,Human_miRNA_ID_3015882 RMVar_hsa_circ_100590,RMVar_hsa_circ_120590,RMVar_hsa_circ_186920,RMVar_hsa_circ_186924 99205 RMVar_ID_99205 Human_SNP_ID_632657113 m1A Human chr17 + 74768726 74768726 74768726 CAGCATTCCACCCCACCTTTTTCCTTCTCCCCAATTACTCCCCTGAATCAATGTACAAATCAGCA CAGCATTCCACCCCACCTTTTTCCTTCTCCCCGATTACTCCCCTGAATCAATGTACAAATCAGCA A G SLC9A3R1 Ensembl:ENSG00000109062 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:74768451..74768800 26863196 MeRIP-seq:(Medium) rs1430832112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47634,Human_RBP_ID_499158,Human_RBP_ID_17654310,Human_RBP_ID_18942079,Human_RBP_ID_20172884,Human_RBP_ID_21890289,Human_RBP_ID_23748283,Human_RBP_ID_24415977,Human_RBP_ID_24481001,Human_RBP_ID_27259256,Human_RBP_ID_27456565,Human_RBP_ID_27561371 Human_miRNA_ID_842877,Human_miRNA_ID_2368096,Human_miRNA_ID_2766035,Human_miRNA_ID_3015882 RMVar_hsa_circ_100590,RMVar_hsa_circ_120590,RMVar_hsa_circ_186920,RMVar_hsa_circ_186924 99206 RMVar_ID_99206 Human_SNP_ID_632657118 m1A Human chr17 - 74768732 74768732 74768732 TGTGGGTGCTGATTTGTACATTGATTCAGGGGAGTAATTGGGGAGAAGGAAAAAGGTGGGGTGGA TGTGGGTGCTGATTTGTACATTGATTCAGGGGGGTAATTGGGGAGAAGGAAAAAGGTGGGGTGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74768451..74768857 26863196 MeRIP-seq:(Medium) rs1303639835 Functional Loss SNV dbSNP153 33..33 33 - - - 99207 RMVar_ID_99207 Human_SNP_ID_632657141 m1A Human chr17 - 74768774 74768774 74768774 AGAACATAGTTCTCTAGAAAAATCATTTGTCAAGAAAGGGGATGTGGGTGCTGATTTGTACATTG AGAACATAGTTCTCTAGAAAAATCATTTGTCAGGAAAGGGGATGTGGGTGCTGATTTGTACATTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:74768751..74768775 26863196 MeRIP-seq:(Medium) rs758258090 Functional Loss SNV dbSNP153 33..33 33 - - - 99208 RMVar_ID_99208 Human_SNP_ID_632657712 m1A Human chr17 + 74770847 74770847 74770847 GTGGAAGGAAACTGGGCCAACTCTACTTTGTAAGCCATAGGGTGCCAGGTAGCCCGGCCACCCTG GTGGAAGGAAACTGGGCCAACTCTACTTTGTAGGCCATAGGGTGCCAGGTAGCCCGGCCACCCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:74770796..74771147 32194978 MeRIP-seq:(Medium) rs1302733633 Functional Loss SNV dbSNP153 33..33 33 - - - 99209 RMVar_ID_99209 Human_SNP_ID_632658609 m1A Human chr17 - 74773662 74773660 74773662 TCCCAGCAGGTACCACGAGTGGATGAAATCAGAGGAGCTGCAGCGTTTGACAGCCTCGGAGCCGC TCCCAGCAGGTACCACGAGTGGATGAAATCAG__GAGCTGCAGCGTTTGACAGCCTCGGAGCCGC CCT C NAT9 Ensembl:ENSG00000109065 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:74773612..74773727 26863196 MeRIP-seq:(Medium) rs1337336170 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1868767,Human_RBP_ID_3950995,Human_RBP_ID_9378908,Human_RBP_ID_18989081,Human_RBP_ID_22959899,Human_RBP_ID_27669399,Human_RBP_ID_27814262 Human_Splice_Rec_1863404,Human_Splice_Rec_1863405,Human_Splice_Rec_1863416,Human_Splice_Rec_1863417,Human_Splice_Rec_1863428,Human_Splice_Rec_1863429,Human_Splice_Rec_1863438,Human_Splice_Rec_1863439,Human_Splice_Rec_1863448,Human_Splice_Rec_1863449,Human_Splice_Rec_1863460,Human_Splice_Rec_1863461,Human_Splice_Rec_1863472,Human_Splice_Rec_1863473,Human_Splice_Rec_1863484,Human_Splice_Rec_1863485,Human_Splice_Rec_1863496,Human_Splice_Rec_1863497,Human_Splice_Rec_1863506,Human_Splice_Rec_1863507,Human_Splice_Rec_1863516,Human_Splice_Rec_1863517,Human_Splice_Rec_1863528,Human_Splice_Rec_1863529,Human_Splice_Rec_1863540,Human_Splice_Rec_1863541,Human_Splice_Rec_1863546,Human_Splice_Rec_1863547,Human_Splice_Rec_1863556,Human_Splice_Rec_1863557,Human_Splice_Rec_1863562,Human_Splice_Rec_1863563,Human_Splice_Rec_1863568,Human_Splice_Rec_1863569,Human_Splice_Rec_1863576,Human_Splice_Rec_1863577,Human_Splice_Rec_1863584,Human_Splice_Rec_1863585,Human_Splice_Rec_1863592,Human_Splice_Rec_1863593,Human_Splice_Rec_1863602,Human_Splice_Rec_1863603,Human_Splice_Rec_1863608,Human_Splice_Rec_1863609,Human_Splice_Rec_1863612,Human_Splice_Rec_1863613,Human_Splice_Rec_1863618,Human_Splice_Rec_1863622,Human_Splice_Rec_1863628,Human_Splice_Rec_1863630 RMVar_hsa_circ_115056,RMVar_hsa_circ_186926,RMVar_hsa_circ_75606,RMVar_hsa_circ_186929 99210 RMVar_ID_99210 Human_SNP_ID_632675163 m1A Human chr17 - 74836137 74836137 74836137 CGGTGAAGGAGAGGAGGCCGTAGAAGGCCAGGATCAGCACGTAGTCCAGGAACACCAGCCTTGTG CGGTGAAGGAGAGGAGGCCGTAGAAGGCCAGGCTCAGCACGTAGTCCAGGAACACCAGCCTTGTG T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:74836053..74836357 26863196 MeRIP-seq:(Medium) rs998129725 Functional Loss SNV dbSNP153 33..33 33 - - - 99211 RMVar_ID_99211 Human_SNP_ID_632676122 m1A Human chr17 + 74839274 74839274 74839274 GACGGGCCCCTAGCCACACAGCTGTCCTCACTACGGGGCAGGGAGCAGCCTCGGCAACAGGCAAA GACGGGCCCCTAGCCACACAGCTGTCCTCACTGCGGGGCAGGGAGCAGCCTCGGCAACAGGCAAA A G TMEM104 Ensembl:ENSG00000109066 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74839228..74839391 26863196 MeRIP-seq:(Medium) rs1383020390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18708152 RMVar_hsa_circ_268070 99212 RMVar_ID_99212 Human_SNP_ID_632685473 m1A Human chr17 + 74868840 74868840 74868840 TCCTGCGACCCCAAATTCCCCTGAACTTGCTGATGACTTTCTACTCTCTCTCTCCTGCCCAGACA TCCTGCGACCCCAAATTCCCCTGAACTTGCTGTTGACTTTCTACTCTCTCTCTCCTGCCCAGACA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74868838..74869101 26863196 MeRIP-seq:(Medium) rs905422304 Functional Loss SNV dbSNP153 33..33 33 - - - 99213 RMVar_ID_99213 Human_SNP_ID_632685475 m1A Human chr17 - 74868847 74868847 74868847 GGGGAGATGTCTGGGCAGGAGAGAGAGAGTAGAAAGTCATCAGCAAGTTCAGGGGAATTTGGGGT GGGGAGATGTCTGGGCAGGAGAGAGAGAGTAGGAAGTCATCAGCAAGTTCAGGGGAATTTGGGGT T C FDXR Ensembl:ENSG00000161513 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:74868837..74869002 26863196 MeRIP-seq:(Medium) rs1259262707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5185564,Human_RBP_ID_13156938 RMVar_hsa_circ_58034 99214 RMVar_ID_99214 Human_SNP_ID_632686393 m1A Human chr17 + 74872305 74872305 74872305 TTTGGCATTTGCAGGGTCTCTTACTTCATCTGAACCCCCAAAGGCTGTGGGTTCATCCAGAGCCC TTTGGCATTTGCAGGGTCTCTTACTTCATCTGGACCCCCAAAGGCTGTGGGTTCATCCAGAGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:74872285..74872369 26863196 MeRIP-seq:(Medium) rs544982043 Functional Loss SNV dbSNP153 33..33 33 - - - 99215 RMVar_ID_99215 Human_SNP_ID_632686467 m1A Human chr17 + 74872568 74872562 74872568 CGTCTTATTCCTACAGATCCCTGTTTCGACTCAGACTTTCCTCTCGCCCCACAGACCTCCGTATC CGTCTTATTCCTACAGATCCCTGTTTC______GACTTTCCTCTCGCCCCACAGACCTCCGTATC CGACTCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:74872330..74872937 26863196 MeRIP-seq:(Medium) rs1343292552 Functional Loss DEL dbSNP153 28..33 33 - - - 99216 RMVar_ID_99216 Human_SNP_ID_632686615 m1A Human chr17 + 74872939 74872939 74872939 GCCGACCAGCCCCACCAGCGCCAGCAGCGCGAAGCCATGGCTGGGAGCAGCAACCTGCAAGTGGA GCCGACCAGCCCCACCAGCGCCAGCAGCGCGAGGCCATGGCTGGGAGCAGCAACCTGCAAGTGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:74872381..74872957 26863196 MeRIP-seq:(Medium) rs1472487009 Functional Loss SNV dbSNP153 33..33 33 - - - 99217 RMVar_ID_99217 Human_SNP_ID_632719689 m1A Human chr17 + 74987710 74987710 74987710 CGCGGACCCGAGCCGGGCAGGGGGCGCCCGCCACGGCACCCGCGCGCTCCTAGCGCCCCAGACCC CGCGGACCCGAGCCGGGCAGGGGGCGCCCGCCTCGGCACCCGCGCGCTCCTAGCGCCCCAGACCC A T CDR2L Ensembl:ENSG00000109089 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74987660..74988159 26863196 MeRIP-seq:(Medium) rs1445979971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17900485 99218 RMVar_ID_99218 Human_SNP_ID_353541685 m1A Human chr8 + 15540378 15540378 15540378 CGGAGGCTGGCCGGGCAGGCGTGGTGCGCGGTAGGAGCTGGGCGCGCACGGCTACCGCGCGTGGA CGGAGGCTGGCCGGGCAGGCGTGGTGCGCGGTGGGAGCTGGGCGCGCACGGCTACCGCGCGTGGA A G TUSC3 Ensembl:ENSG00000104723 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:15540276..15540475 26863410 MeRIP-seq:(Medium) rs967573621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696292,Human_RBP_ID_4976283 99219 RMVar_ID_99219 Human_SNP_ID_354125983 m1A Human chr8 - 17246728 17246728 17246728 CGCTACCGCCACCGCCACCGCCACCGCCGCCGAGTGCTGTCTCTATGGCGAGGAGGAGGAGGAGG CGCTACCGCCACCGCCACCGCCACCGCCGCCGGGTGCTGTCTCTATGGCGAGGAGGAGGAGGAGG T C CNOT7 Ensembl:ENSG00000198791 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr8:17246678..17246806;chr8:17246676..17246850 26863196,32194978,32194978 MeRIP-seq:(Medium) rs912063177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994912,Human_RBP_ID_17434092,Human_RBP_ID_21905658,Human_RBP_ID_27364701 Human_Splice_Rec_951089,Human_Splice_Rec_951103,Human_Splice_Rec_951113,Human_Splice_Rec_951143,Human_Splice_Rec_951155,Human_Splice_Rec_951163 99220 RMVar_ID_99220 Human_SNP_ID_354125986 m1A Human chr8 - 17246744 17246732 17246744 CACCCGCTGCCGCCGCCGCTACCGCCACCGCCACCGCCACCGCCGCCGAGTGCTGTCTCTATGGC CACCCGCTGCCGCCGCCGCTACCGCCACCGCC____________GCCGAGTGCTGTCTCTATGGC CGGCGGTGGCGGT C CNOT7 Ensembl:ENSG00000198791 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:17246676..17246800 26863410 MeRIP-seq:(Medium) rs897428567 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_4994912,Human_RBP_ID_5481408,Human_RBP_ID_9338182,Human_RBP_ID_17433786,Human_RBP_ID_21905658 Human_Splice_Rec_951089,Human_Splice_Rec_951103,Human_Splice_Rec_951113,Human_Splice_Rec_951143,Human_Splice_Rec_951155,Human_Splice_Rec_951163 99221 RMVar_ID_99221 Human_SNP_ID_354125987 m1A Human chr8 - 17246744 17246732 17246744 CACCCGCTGCCGCCGCCGCTACCGCCACCGCCACCGCCACCGCCGCCGAGTGCTGTCTCTATGGC CACCCGCTGCCGCCGCCGCTACCGCCACCGCC______ACCGCCGCCGAGTGCTGTCTCTATGGC CGGCGGTGGCGGT CGGCGGT CNOT7 Ensembl:ENSG00000198791 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:17246676..17246800 26863410 MeRIP-seq:(Medium) rs897428567 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4994912,Human_RBP_ID_5481408,Human_RBP_ID_9338182,Human_RBP_ID_17433786,Human_RBP_ID_21905658 Human_Splice_Rec_951089,Human_Splice_Rec_951103,Human_Splice_Rec_951113,Human_Splice_Rec_951143,Human_Splice_Rec_951155,Human_Splice_Rec_951163 99222 RMVar_ID_99222 Human_SNP_ID_354126006 m1A Human chr8 - 17246756 17246756 17246756 GTGTCTATGGGGCACCCGCTGCCGCCGCCGCTACCGCCACCGCCACCGCCACCGCCGCCGAGTGC GTGTCTATGGGGCACCCGCTGCCGCCGCCGCTTCCGCCACCGCCACCGCCACCGCCGCCGAGTGC T A CNOT7 Ensembl:ENSG00000198791 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:17246685..17246777 26863410 MeRIP-seq:(Medium) rs573336162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4976596,Human_RBP_ID_5481408,Human_RBP_ID_9338182,Human_RBP_ID_17433786,Human_RBP_ID_18452383,Human_RBP_ID_21905658 Human_Splice_Rec_951089,Human_Splice_Rec_951103,Human_Splice_Rec_951113,Human_Splice_Rec_951143,Human_Splice_Rec_951155,Human_Splice_Rec_951163 99223 RMVar_ID_99223 Human_SNP_ID_354126007 m1A Human chr8 - 17246756 17246756 17246756 GTGTCTATGGGGCACCCGCTGCCGCCGCCGCTACCGCCACCGCCACCGCCACCGCCGCCGAGTGC GTGTCTATGGGGCACCCGCTGCCGCCGCCGCTGCCGCCACCGCCACCGCCACCGCCGCCGAGTGC T C CNOT7 Ensembl:ENSG00000198791 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:17246685..17246777 26863410 MeRIP-seq:(Medium) rs573336162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4976596,Human_RBP_ID_5481408,Human_RBP_ID_9338182,Human_RBP_ID_17433786,Human_RBP_ID_18452383,Human_RBP_ID_21905658 Human_Splice_Rec_951089,Human_Splice_Rec_951103,Human_Splice_Rec_951113,Human_Splice_Rec_951143,Human_Splice_Rec_951155,Human_Splice_Rec_951163 99224 RMVar_ID_99224 Human_SNP_ID_354126013 m1A Human chr8 + 17246769 17246769 17246769 GTGGCGGTGGCGGTGGCGGTAGCGGCGGCGGCAGCGGGTGCCCCATAGACACCTCTCGCCCAGCG GTGGCGGTGGCGGTGGCGGTAGCGGCGGCGGCTGCGGGTGCCCCATAGACACCTCTCGCCCAGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:17246676..17246850 26863196 MeRIP-seq:(Medium) rs1444033044 Functional Loss SNV dbSNP153 33..33 33 - - - 99225 RMVar_ID_99225 Human_SNP_ID_354212456 m1A Human chr8 - 17497211 17497211 17497211 ACTTACTGGGGCTGGGTTGGGGTCGCGCCAAGAAGGCGGCGGTGGGCTGCCGGCTGCAGCGCGTC ACTTACTGGGGCTGGGTTGGGGTCGCGCCAAGCAGGCGGCGGTGGGCTGCCGGCTGCAGCGCGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:17497108..17497250 26863196 MeRIP-seq:(Medium) rs1226557076 Functional Loss SNV dbSNP153 33..33 33 - - - 99226 RMVar_ID_99226 Human_SNP_ID_354227474 m1A Human chr8 + 17543287 17543287 17543287 TAGGTTACCAAAGGGAGGGATGACAATTCCAGATCAGCTTCTAACCTCCTCCCTTCTGCTCAGGT TAGGTTACCAAAGGGAGGGATGACAATTCCAGGTCAGCTTCTAACCTCCTCCCTTCTGCTCAGGT A G SLC7A2 Ensembl:ENSG00000003989 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:17543284..17543412 26863196 MeRIP-seq:(Medium) rs1248234113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958821 RMVar_hsa_circ_123243,RMVar_hsa_circ_250403 99227 RMVar_ID_99227 Human_SNP_ID_354238520 m1A Human chr8 + 17577293 17577293 17577293 CTGGCTGCTGCTTGGTCTTCTGCTGGTGCACGAAGCGCTGGAGGATGGTGAGTGACTCTGGGCGC CTGGCTGCTGCTTGGTCTTCTGCTGGTGCACGCAGCGCTGGAGGATGGTGAGTGACTCTGGGCGC A C PDGFRL Ensembl:ENSG00000104213 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:17577248..17577324 26863196 MeRIP-seq:(Medium) rs1306778198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_951521,Human_Splice_Rec_951533,Human_Splice_Rec_951537 99228 RMVar_ID_99228 Human_SNP_ID_354258698 m1A Human chr8 - 17631821 17631821 17631821 TTTCAAAGTTGATAGAAGGCTAAGAGCTGACCAAGAAGAGTGAGAAAGCTGTGGGGGAGGTGGGG TTTCAAAGTTGATAGAAGGCTAAGAGCTGACCCAGAAGAGTGAGAAAGCTGTGGGGGAGGTGGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:17631797..17631910 26863196 MeRIP-seq:(Medium) rs1174621375 Functional Loss SNV dbSNP153 33..33 33 - - - 99229 RMVar_ID_99229 Human_SNP_ID_354292681 m1A Human chr8 - 17723769 17723769 17723769 TCATGGGTGAATTTGCCTAGACCACTTCCTAAATCCAAAGCATCTTTGAAAAGTCCTGCGCTGCG TCATGGGTGAATTTGCCTAGACCACTTCCTAAGTCCAAAGCATCTTTGAAAAGTCCTGCGCTGCG T C MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:17723717..17723844 26863196 MeRIP-seq:(Medium) rs1436451393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_951630,Human_Splice_Rec_951631,Human_Splice_Rec_951676,Human_Splice_Rec_951677,Human_Splice_Rec_951824,Human_Splice_Rec_951825,Human_Splice_Rec_951831,Human_Splice_Rec_951848 RMVar_hsa_circ_110290,RMVar_hsa_circ_355319,RMVar_hsa_circ_25812,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_318393,RMVar_hsa_circ_359875,RMVar_hsa_circ_250419,RMVar_hsa_circ_354851,RMVar_hsa_circ_346488,RMVar_hsa_circ_350774,RMVar_hsa_circ_356579,RMVar_hsa_circ_62583,RMVar_hsa_circ_250424,RMVar_hsa_circ_363136,RMVar_hsa_circ_332920 99230 RMVar_ID_99230 Human_SNP_ID_354295937 m1A Human chr8 - 17732775 17732775 17732775 ATTGGGGGTGAGAGCAAAGGGAGGAGTCACGGATGAACATGACCATGTTGGTGTGAGCAATGGAA ATTGGGGGTGAGAGCAAAGGGAGGAGTCACGGGTGAACATGACCATGTTGGTGTGAGCAATGGAA T C MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:17732731..17732796 26863196 MeRIP-seq:(Medium) rs543823769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110290,RMVar_hsa_circ_355319,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_354851,RMVar_hsa_circ_350774,RMVar_hsa_circ_356579,RMVar_hsa_circ_62583,RMVar_hsa_circ_332920 99231 RMVar_ID_99231 Human_SNP_ID_354365020 m1A Human chr8 + 17923049 17923049 17923049 CGGCGGTTGGCGCTGCGTAGCTGAGGTCGAAAAGGCGGCCACTGGGGCCGAGGCAGCCAGGAAAC CGGCGGTTGGCGCTGCGTAGCTGAGGTCGAAAGGGCGGCCACTGGGGCCGAGGCAGCCAGGAAAC A G PCM1 Ensembl:ENSG00000078674 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:17923001..17923200 26863196 MeRIP-seq:(Medium) rs960380181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255246,Human_RBP_ID_796643,Human_RBP_ID_4995351,Human_RBP_ID_5534077,Human_RBP_ID_8922866,Human_RBP_ID_9405999,Human_RBP_ID_24549545 99232 RMVar_ID_99232 Human_SNP_ID_354365038 m1A Human chr8 - 17923098 17923098 17923098 GCCGCCGGCAGCGGTCGGCCCTCGGAGACCGCAGCAGAGAGGCCCACACGTTTCCTGGCTGCCTC GCCGCCGGCAGCGGTCGGCCCTCGGAGACCGCGGCAGAGAGGCCCACACGTTTCCTGGCTGCCTC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:17923050..17923213 26863196 MeRIP-seq:(Medium) rs1451653183 Functional Loss SNV dbSNP153 33..33 33 - - - 99233 RMVar_ID_99233 Human_SNP_ID_354398399 m1A Human chr8 + 18011826 18011818 18011827 TGAAGCTACTGAAGAAAATGAACATGATGAACAGGTATTCCCGTATTGACTGACACACTTCCATC TGAAGCTACTGAAGAAAATGAACAT_________GTATTCCCGTATTGACTGACACACTTCCATC TGATGAACAG T PCM1 Ensembl:ENSG00000078674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:18011777..18011863 26863196 MeRIP-seq:(Medium) rs1360593077 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_9405214,Human_RBP_ID_23117106,Human_RBP_ID_24549441,Human_RBP_ID_27831707 Human_Splice_Rec_952061,Human_Splice_Rec_952135,Human_Splice_Rec_952285,Human_Splice_Rec_952357,Human_Splice_Rec_952407 RMVar_hsa_circ_110654,RMVar_hsa_circ_250429,RMVar_hsa_circ_54669,RMVar_hsa_circ_27948,RMVar_hsa_circ_250447,RMVar_hsa_circ_312989,RMVar_hsa_circ_5919,RMVar_hsa_circ_313842,RMVar_hsa_circ_281177,RMVar_hsa_circ_96382,RMVar_hsa_circ_250458,RMVar_hsa_circ_250459,RMVar_hsa_circ_265558,RMVar_hsa_circ_250461,RMVar_hsa_circ_268506,RMVar_hsa_circ_99262,RMVar_hsa_circ_250464,RMVar_hsa_circ_267280,RMVar_hsa_circ_31286,RMVar_hsa_circ_268606,RMVar_hsa_circ_268972,RMVar_hsa_circ_354218,RMVar_hsa_circ_62126,RMVar_hsa_circ_56698,RMVar_hsa_circ_250471,RMVar_hsa_circ_297075,RMVar_hsa_circ_55218,RMVar_hsa_circ_250473,RMVar_hsa_circ_57292,RMVar_hsa_circ_250478,RMVar_hsa_circ_69268,RMVar_hsa_circ_302541,RMVar_hsa_circ_309332,RMVar_hsa_circ_364044,RMVar_hsa_circ_329974,RMVar_hsa_circ_361075,RMVar_hsa_circ_352457,RMVar_hsa_circ_358092,RMVar_hsa_circ_283691,RMVar_hsa_circ_57932,RMVar_hsa_circ_250479,RMVar_hsa_circ_56991 99234 RMVar_ID_99234 Human_SNP_ID_354404943 m1A Human chr8 - 18029043 18029043 18029043 GGGTTCAGGCTATTCTCCTGCCTTAGCCTCCCAAGTAGCTAGGACTACAGGCACGTGCCACCTCT GGGTTCAGGCTATTCTCCTGCCTTAGCCTCCCGAGTAGCTAGGACTACAGGCACGTGCCACCTCT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:18029019..18029101 26863410 MeRIP-seq:(Medium) rs760884008 Functional Loss SNV dbSNP153 33..33 33 - - - 99235 RMVar_ID_99235 Human_SNP_ID_354422361 m1A Human chr8 - 18081230 18081230 18081230 GAGGGCGAATGAGCTGAAGGAATCGTTGGGTGAGGATGAGGGAGTGAGGTGTCAGCGTGACCTGC GAGGGCGAATGAGCTGAAGGAATCGTTGGGTGCGGATGAGGGAGTGAGGTGTCAGCGTGACCTGC T G ASAH1 Ensembl:ENSG00000104763 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:18081228..18081342 26863196 MeRIP-seq:(Medium) rs371983010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8684228 RMVar_hsa_circ_32680 99236 RMVar_ID_99236 Human_SNP_ID_354807235 m1A Human chr8 - 19314048 19314043 19314048 CCTAGCCAGCGGCTCCAGACACCGGACACCGGACACCGGACACCGGACACCCGCCGCGGCCGCTC CCTAGCCAGCGGCTCCAGACACCGGACACCGG_____GGACACCGGACACCCGCCGCGGCCGCTC CGGTGT C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:19313937..19314127;chr8:19313714..19314136 26863196 MeRIP-seq:(Medium) rs1357508109 Functional Loss DEL dbSNP153 33..37 33 - - - 99237 RMVar_ID_99237 Human_SNP_ID_354807238 m1A Human chr8 - 19314048 19314048 19314048 CCTAGCCAGCGGCTCCAGACACCGGACACCGGACACCGGACACCGGACACCCGCCGCGGCCGCTC CCTAGCCAGCGGCTCCAGACACCGGACACCGGGCACCGGACACCGGACACCCGCCGCGGCCGCTC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:19313937..19314127;chr8:19313714..19314136 26863196 MeRIP-seq:(Medium) rs1210378509 Functional Loss SNV dbSNP153 33..33 33 - - - 99238 RMVar_ID_99238 Human_SNP_ID_354812875 m1A Human chr8 + 19333007 19333007 19333007 TGGAAACTTGGAGCTGATAAGGAAGTCTGGGTATGGGTGATGGGCGAACACCATCTAGATAAACC TGGAAACTTGGAGCTGATAAGGAAGTCTGGGTGTGGGTGATGGGCGAACACCATCTAGATAAACC A G SH2D4A Ensembl:ENSG00000104611 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:19332914..19333036 26863196 MeRIP-seq:(Medium) rs142724341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_953984,Human_Splice_Rec_954000,Human_Splice_Rec_954018,Human_Splice_Rec_954034 RMVar_hsa_circ_76118,RMVar_hsa_circ_107281,RMVar_hsa_circ_127659,RMVar_hsa_circ_250525,RMVar_hsa_circ_250526,RMVar_hsa_circ_357123,RMVar_hsa_circ_57089,RMVar_hsa_circ_250527,RMVar_hsa_circ_250528,RMVar_hsa_circ_250529,RMVar_hsa_circ_357446 99239 RMVar_ID_99239 Human_SNP_ID_354813416 m1A Human chr8 + 19334811 19334811 19334811 CTGGAAGAAAGTGGCAGAAAAGGAGGAACTGGAGCAAGGATCGAGGCCAGCACCAACCCTGGAAG CTGGAAGAAAGTGGCAGAAAAGGAGGAACTGGGGCAAGGATCGAGGCCAGCACCAACCCTGGAAG A G SH2D4A Ensembl:ENSG00000104611 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:19334760..19334897 26863196 MeRIP-seq:(Medium) rs760731401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88239,Human_RBP_ID_958844,Human_RBP_ID_9405234,Human_RBP_ID_19139932 Human_Splice_Rec_953987,Human_Splice_Rec_954003,Human_Splice_Rec_954021,Human_Splice_Rec_954037 Human_miRNA_ID_313867,Human_miRNA_ID_1564980,Human_miRNA_ID_2070241,Human_miRNA_ID_2070242,Human_miRNA_ID_2490146,Human_miRNA_ID_2490147,Human_miRNA_ID_2803151,Human_miRNA_ID_2803152 RMVar_hsa_circ_76118,RMVar_hsa_circ_107281,RMVar_hsa_circ_127659,RMVar_hsa_circ_250525,RMVar_hsa_circ_250526,RMVar_hsa_circ_357123,RMVar_hsa_circ_57089,RMVar_hsa_circ_250527,RMVar_hsa_circ_250528,RMVar_hsa_circ_250529,RMVar_hsa_circ_357446 99240 RMVar_ID_99240 Human_SNP_ID_354831464 m1A Human chr8 + 19395651 19395651 19395651 ACCAGGGGACAAGAGGCAAGTTGGAGTGATGCAGCCGGAAGGGAAGGGACACCAAGGATCTCCGG ACCAGGGGACAAGAGGCAAGTTGGAGTGATGCGGCCGGAAGGGAAGGGACACCAAGGATCTCCGG A G SH2D4A Ensembl:ENSG00000104611 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:19395600..19395701 26863196 MeRIP-seq:(Medium) rs1408535484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27537234 RMVar_hsa_circ_76118,RMVar_hsa_circ_107281,RMVar_hsa_circ_127659,RMVar_hsa_circ_250525,RMVar_hsa_circ_250526,RMVar_hsa_circ_250528 99241 RMVar_ID_99241 Human_SNP_ID_354862258 m1A Human chr8 - 19482445 19482445 19482445 GCAGAAGAAGTCATTGCTGGCCTGGATTGGGGAGAGAACATCATCAGTGGAGTGGTAGGGGCAGA GCAGAAGAAGTCATTGCTGGCCTGGATTGGGGGGAGAACATCATCAGTGGAGTGGTAGGGGCAGA T C CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:19482440..19482523 26863196 MeRIP-seq:(Medium) rs1054340308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5576,RMVar_hsa_circ_53361,RMVar_hsa_circ_285282 99242 RMVar_ID_99242 Human_SNP_ID_354927721 m1A Human chr8 - 19669950 19669950 19669950 AAGAAATGGGAAAGGAGGCATTTTGAGGGGAGAGTGAGTTGTTTGTCCACAGGACTGCAGGAGAC AAGAAATGGGAAAGGAGGCATTTTGAGGGGAGCGTGAGTTGTTTGTCCACAGGACTGCAGGAGAC T G CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:19669940..19670128 26863196 MeRIP-seq:(Medium) rs1331292392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45837,RMVar_hsa_circ_340519 99243 RMVar_ID_99243 Human_SNP_ID_354935703 m1A Human chr8 + 19693526 19693526 19693526 AGTGCTCCTATTTTATTGCATGGGCCATGACTAATGCAGCCTCCTCTCATGTCTTCAATCTTGAT AGTGCTCCTATTTTATTGCATGGGCCATGACTGATGCAGCCTCCTCTCATGTCTTCAATCTTGAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:19693515..19693720 26863196 MeRIP-seq:(Medium) rs1283510015 Functional Loss SNV dbSNP153 33..33 33 - - - 99244 RMVar_ID_99244 Human_SNP_ID_354952042 m1A Human chr8 - 19751743 19751743 19751743 GCCAAGGGGGAAGTGCTACACACTTGCAAACAACCAGATCTCATGAGAACTCTATCACGAGAACA GCCAAGGGGGAAGTGCTACACACTTGCAAACAGCCAGATCTCATGAGAACTCTATCACGAGAACA T C CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:19751741..19751910 26863196 MeRIP-seq:(Medium) rs1345837971 Functional Loss SNV dbSNP153 33..33 33 - - - 99245 RMVar_ID_99245 Human_SNP_ID_354953834 m1A Human chr8 - 19757252 19757252 19757252 GGGAGGTGGAGCCGAGTCCGCGGCGGCCGCGCAGGAGGGAAAGTTCAGCGACGGCGGCAGCGGCC GGGAGGTGGAGCCGAGTCCGCGGCGGCCGCGCCGGAGGGAAAGTTCAGCGACGGCGGCAGCGGCC T G CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:19757132..19757267 26863196 MeRIP-seq:(Medium) rs1388646058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_954139,Human_Splice_Rec_954153 99246 RMVar_ID_99246 Human_SNP_ID_354971612 m1A Human chr8 + 19818294 19818294 19818294 ATGTGTGTTGCAGTATGAGATGTACACCATCGAGCGGAATGCAGAGCGGACCGCCACCGCCGGGA ATGTGTGTTGCAGTATGAGATGTACACCATCGGGCGGAATGCAGAGCGGACCGCCACCGCCGGGA A G INTS10 Ensembl:ENSG00000104613 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:19817637..19818364 26863196 MeRIP-seq:(Medium) rs1181273669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796711,Human_RBP_ID_958848,Human_RBP_ID_1694855,Human_RBP_ID_4977927,Human_RBP_ID_9406040,Human_RBP_ID_18124825,Human_RBP_ID_24252510,Human_RBP_ID_26554460 Human_Splice_Rec_954176,Human_Splice_Rec_954180,Human_Splice_Rec_954181,Human_Splice_Rec_954213,Human_Splice_Rec_954218,Human_Splice_Rec_954220,Human_Splice_Rec_954221,Human_Splice_Rec_954226,Human_Splice_Rec_954227 RMVar_hsa_circ_43432,RMVar_hsa_circ_64903,RMVar_hsa_circ_364148 99247 RMVar_ID_99247 Human_SNP_ID_354971753 m1A Human chr8 - 19818863 19818863 19818863 TAAATGTCTACCAAGAAGAGAGTGTCTACGAAATACTACACAGGCATGAAAAGGAATGAAGTGGA TAAATGTCTACCAAGAAGAGAGTGTCTACGAAGTACTACACAGGCATGAAAAGGAATGAAGTGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:19818860..19820512 32194978 MeRIP-seq:(Medium) rs181819614 Functional Loss SNV dbSNP153 33..33 33 - - - 99248 RMVar_ID_99248 Human_SNP_ID_354980567 m1A Human chr8 + 19851735 19851735 19851735 GGCCATGGAGCGCCAGGTCTCCCGCTGTGGAGAGAATCTGATGGTGGTTCTGCACAGGTTCTGCA GGCCATGGAGCGCCAGGTCTCCCGCTGTGGAGGGAATCTGATGGTGGTTCTGCACAGGTTCTGCA A G INTS10 Ensembl:ENSG00000104613 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:19851684..19851884 32194978 MeRIP-seq:(Medium) rs984497704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88268,Human_RBP_ID_696975,Human_RBP_ID_845798,Human_RBP_ID_8684498,Human_RBP_ID_9405237,Human_RBP_ID_22114832,Human_RBP_ID_23088041 Human_Splice_Rec_954210,Human_Splice_Rec_954280,Human_Splice_Rec_954290,Human_Splice_Rec_954298,Human_Splice_Rec_954300,Human_Splice_Rec_954302 RMVar_hsa_circ_109555,RMVar_hsa_circ_93343,RMVar_hsa_circ_250578,RMVar_hsa_circ_250579 99249 RMVar_ID_99249 Human_SNP_ID_355006832 m1A Human chr8 + 19939349 19939349 19939349 CATCCCCTTTAAAGGGCGACTTGCTCAGCGCCAAACCGCGGCTCCAGCCCTCTCCAGCCTCCGGC CATCCCCTTTAAAGGGCGACTTGCTCAGCGCCGAACCGCGGCTCCAGCCCTCTCCAGCCTCCGGC A G LPL Ensembl:ENSG00000175445 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:19939305..19939431;chr8:19939300..19939457 26863196 MeRIP-seq:(Medium) rs1386508757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_954312 99250 RMVar_ID_99250 Human_SNP_ID_355014731 m1A Human chr8 - 19966297 19966297 19966297 TAGAAGCTCACACAATGCAAAATTTGAACTCAAACCTATCTTTTCATGTCAAAGCCAGGAACAAA TAGAAGCTCACACAATGCAAAATTTGAACTCATACCTATCTTTTCATGTCAAAGCCAGGAACAAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:19966248..19966387 26863196 MeRIP-seq:(Medium) rs1433624187 Functional Loss SNV dbSNP153 33..33 33 - - - 99251 RMVar_ID_99251 Human_SNP_ID_355014805 m1A Human chr8 + 19966560 19966560 19966560 GCTCTTCTACGTATAAATATGAAATGATAAAGATGTCAAATATCTCAGAGGCTATAGCTGGGAAC GCTCTTCTACGTATAAATATGAAATGATAAAGGTGTCAAATATCTCAGAGGCTATAGCTGGGAAC A G LPL Ensembl:ENSG00000175445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3200218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1413348 Clinvar_Rec_610 GWAS_ID_13078,GWAS_ID_13079,GWAS_ID_13080,GWAS_ID_13081,GWAS_ID_13082,GWAS_ID_13083,GWAS_ID_13084,GWAS_ID_13085,GWAS_ID_13086,GWAS_ID_13087,GWAS_ID_13088,GWAS_ID_13089,GWAS_ID_13090,GWAS_ID_13091,GWAS_ID_13092,GWAS_ID_13093,GWAS_ID_13094,GWAS_ID_13095,GWAS_ID_13096,GWAS_ID_13097,GWAS_ID_13098,GWAS_ID_13099,GWAS_ID_13100,GWAS_ID_13101,GWAS_ID_13102,GWAS_ID_13103,GWAS_ID_13104,GWAS_ID_13105,GWAS_ID_13106,GWAS_ID_13107,GWAS_ID_13108,GWAS_ID_13109,GWAS_ID_13110,GWAS_ID_13111 99252 RMVar_ID_99252 Human_SNP_ID_355014806 m1A Human chr8 + 19966560 19966560 19966560 GCTCTTCTACGTATAAATATGAAATGATAAAGATGTCAAATATCTCAGAGGCTATAGCTGGGAAC GCTCTTCTACGTATAAATATGAAATGATAAAGTTGTCAAATATCTCAGAGGCTATAGCTGGGAAC A T LPL Ensembl:ENSG00000175445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3200218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1413348 Clinvar_Rec_610 GWAS_ID_13078,GWAS_ID_13079,GWAS_ID_13080,GWAS_ID_13081,GWAS_ID_13082,GWAS_ID_13083,GWAS_ID_13084,GWAS_ID_13085,GWAS_ID_13086,GWAS_ID_13087,GWAS_ID_13088,GWAS_ID_13089,GWAS_ID_13090,GWAS_ID_13091,GWAS_ID_13092,GWAS_ID_13093,GWAS_ID_13094,GWAS_ID_13095,GWAS_ID_13096,GWAS_ID_13097,GWAS_ID_13098,GWAS_ID_13099,GWAS_ID_13100,GWAS_ID_13101,GWAS_ID_13102,GWAS_ID_13103,GWAS_ID_13104,GWAS_ID_13105,GWAS_ID_13106,GWAS_ID_13107,GWAS_ID_13108,GWAS_ID_13109,GWAS_ID_13110,GWAS_ID_13111 99253 RMVar_ID_99253 Human_SNP_ID_355086706 m1A Human chr8 + 20197438 20197438 20197438 GATGGCGCTGCGGGCGATGCGGGGGATTGTCAACGGGGCCGCACCCGAGCTACCCGTGCCCACCG GATGGCGCTGCGGGCGATGCGGGGGATTGTCAGCGGGGCCGCACCCGAGCTACCCGTGCCCACCG A G ATP6V1B2 Ensembl:ENSG00000147416 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:20197366..20197550 26863196 MeRIP-seq:(Medium) rs762637201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994929,Human_RBP_ID_22465113,Human_RBP_ID_22626064,Human_RBP_ID_26832597 99254 RMVar_ID_99254 Human_SNP_ID_355091717 m1A Human chr8 + 20214806 20214806 20214806 TTGTAATATCGTGCATGATACTCTTCTGCTTGACCTGCTGTCAGGTTTCAGCAGCCAGGGAAGAG TTGTAATATCGTGCATGATACTCTTCTGCTTGTCCTGCTGTCAGGTTTCAGCAGCCAGGGAAGAG A T ATP6V1B2 Ensembl:ENSG00000147416 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:20214800..20214901 32194978 MeRIP-seq:(Medium) rs755395741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23949,RMVar_hsa_circ_13399 99255 RMVar_ID_99255 Human_SNP_ID_355590148 m1A Human chr8 + 21919768 21919767 21919768 GAGGGGGGGCCGGAGAGGAGCATGAATGGAGCAAAATGGCGGATCATGTGCAGGTGAGAGGAGCC GAGGGGGGGCCGGAGAGGAGCATGAATGGAGC_AAATGGCGGATCATGTGCAGGTGAGAGGAGCC CA C XPO7 Ensembl:ENSG00000130227 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:21919717..21919835 26863196 MeRIP-seq:(Medium) rs1457620914 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_795610,Human_RBP_ID_845658,Human_RBP_ID_4995361,Human_RBP_ID_9338606,Human_RBP_ID_18426668 Human_Splice_Rec_954977,Human_Splice_Rec_955029,Human_Splice_Rec_955039 RMVar_hsa_circ_250593,RMVar_hsa_circ_119137,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,RMVar_hsa_circ_250595 99256 RMVar_ID_99256 Human_SNP_ID_355590155 m1A Human chr8 - 21919784 21919784 21919784 GCCCCCTCCCCCCCGCGGCTCCTCTCACCTGCACATGATCCGCCATTTTGCTCCATTCATGCTCC GCCCCCTCCCCCCCGCGGCTCCTCTCACCTGCCCATGATCCGCCATTTTGCTCCATTCATGCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:21919695..21919842 26863196 MeRIP-seq:(Medium) rs1179733582 Functional Loss SNV dbSNP153 33..33 33 - - - 99257 RMVar_ID_99257 Human_SNP_ID_355610432 m1A Human chr8 + 21994426 21994426 21994426 GAGGGATCGCTTTCGCTTTCAATGCCAAGACCAGCTTCATGATGCTCTTTGAATGGATGTATCCT GAGGGATCGCTTTCGCTTTCAATGCCAAGACCCGCTTCATGATGCTCTTTGAATGGATGTATCCT A C XPO7 Ensembl:ENSG00000130227 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:21994375..21995516 32194978 MeRIP-seq:(Medium) rs761119609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1694929,Human_RBP_ID_2054109,Human_RBP_ID_18388818 Human_Splice_Rec_955012,Human_Splice_Rec_955013,Human_Splice_Rec_955094,Human_Splice_Rec_955095,Human_Splice_Rec_955112,Human_Splice_Rec_955113 Human_miRNA_ID_1988267 RMVar_hsa_circ_5827,RMVar_hsa_circ_250593,RMVar_hsa_circ_119137,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,RMVar_hsa_circ_250595,RMVar_hsa_circ_310810,RMVar_hsa_circ_324883,RMVar_hsa_circ_102919,RMVar_hsa_circ_110518,RMVar_hsa_circ_250599,RMVar_hsa_circ_250600,RMVar_hsa_circ_116142,RMVar_hsa_circ_92609,RMVar_hsa_circ_250603,RMVar_hsa_circ_30353,RMVar_hsa_circ_250601,RMVar_hsa_circ_250602,RMVar_hsa_circ_94423,RMVar_hsa_circ_107623,RMVar_hsa_circ_250614,RMVar_hsa_circ_44806,RMVar_hsa_circ_321844,RMVar_hsa_circ_361382,RMVar_hsa_circ_250615,RMVar_hsa_circ_60352,RMVar_hsa_circ_119847,RMVar_hsa_circ_85146,RMVar_hsa_circ_82787,RMVar_hsa_circ_250616,RMVar_hsa_circ_88291,RMVar_hsa_circ_250626,RMVar_hsa_circ_110972,RMVar_hsa_circ_250628,RMVar_hsa_circ_250627,RMVar_hsa_circ_101216,RMVar_hsa_circ_80018,RMVar_hsa_circ_91053,RMVar_hsa_circ_250634,RMVar_hsa_circ_250635,RMVar_hsa_circ_250637,RMVar_hsa_circ_80679,RMVar_hsa_circ_250636,RMVar_hsa_circ_82058,RMVar_hsa_circ_96001,RMVar_hsa_circ_250638,RMVar_hsa_circ_250639,RMVar_hsa_circ_250641,RMVar_hsa_circ_324826,RMVar_hsa_circ_83467,RMVar_hsa_circ_18506,RMVar_hsa_circ_118937,RMVar_hsa_circ_250645,RMVar_hsa_circ_81384,RMVar_hsa_circ_250646,RMVar_hsa_circ_329970,RMVar_hsa_circ_250648,RMVar_hsa_circ_127593,RMVar_hsa_circ_250650,RMVar_hsa_circ_111443,RMVar_hsa_circ_250652,RMVar_hsa_circ_75640,RMVar_hsa_circ_250653,RMVar_hsa_circ_250651,RMVar_hsa_circ_118909,RMVar_hsa_circ_250649,RMVar_hsa_circ_327796,RMVar_hsa_circ_102498,RMVar_hsa_circ_250655,RMVar_hsa_circ_250656 99258 RMVar_ID_99258 Human_SNP_ID_355612612 m1A Human chr8 - 22002154 22002154 22002154 TACGTGACAGCTGCTTGAAGAGGTATGTCACAATGTGGTCCAGGCAGGAGCAGCAGCCTGTGCAT TACGTGACAGCTGCTTGAAGAGGTATGTCACAGTGTGGTCCAGGCAGGAGCAGCAGCCTGTGCAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:21999650..22002187 32194978 MeRIP-seq:(Medium) rs1170573358 Functional Loss SNV dbSNP153 33..33 33 - - - 99259 RMVar_ID_99259 Human_SNP_ID_355613419 m1A Human chr8 - 22005243 22005243 22005243 CCCTGCCCCCTAGTGAGTGTACTCACACCCCTATTCCCTGGGGAAGCAGCTAGTTGACCTTTGCC CCCTGCCCCCTAGTGAGTGTACTCACACCCCTGTTCCCTGGGGAAGCAGCTAGTTGACCTTTGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22005192..22005350 26863196 MeRIP-seq:(Medium) rs559605577 Functional Loss SNV dbSNP153 33..33 33 - - - 99260 RMVar_ID_99260 Human_SNP_ID_355613577 m1A Human chr8 - 22005851 22005851 22005851 TGAGGGTAAGCAAAGTAGGAAAGAGGGTGGAGATAAGAACACCAAACACTTTTAGCTGGAGTTAT TGAGGGTAAGCAAAGTAGGAAAGAGGGTGGAGGTAAGAACACCAAACACTTTTAGCTGGAGTTAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22005801..22006025 26863196 MeRIP-seq:(Medium) rs141324840 Functional Loss SNV dbSNP153 33..33 33 - - - 99261 RMVar_ID_99261 Human_SNP_ID_355631605 m1A Human chr8 + 22068607 22068606 22068608 GAGAGAGGGATAGAGGAGAAAGAATAAGAGACAAGAGAGAAGAAAGTGGAGAGAGAGAGGAAGGA GAGAGAGGGATAGAGGAGAAAGAATAAGAGAC__GAGAGAAGAAAGTGGAGAGAGAGAGGAAGGA CAA C DMTN Ensembl:ENSG00000158856 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22068605..22068688 26863196 MeRIP-seq:(Medium) rs770430054 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_34908,RMVar_hsa_circ_28452,RMVar_hsa_circ_63604 99262 RMVar_ID_99262 Human_SNP_ID_355632026 m1A Human chr8 - 22069850 22069850 22069850 CTCTGTGGGAGGAAGAACAGATGAGGAGGAGGACATGCTGATGGCAGGGAGGCTGGGGCCAGGAG CTCTGTGGGAGGAAGAACAGATGAGGAGGAGGCCATGCTGATGGCAGGGAGGCTGGGGCCAGGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22069847..22069955 26863196 MeRIP-seq:(Medium) rs1193291957 Functional Loss SNV dbSNP153 33..33 33 - - - 99263 RMVar_ID_99263 Human_SNP_ID_355632150 m1A Human chr8 + 22070146 22070146 22070146 GAGGGGTGAAGGTAGCCAAGTTGGCCTCGGGCAGGGCACACCTGGCTGACCCTGGCCTTTGTCTG GAGGGGTGAAGGTAGCCAAGTTGGCCTCGGGCGGGGCACACCTGGCTGACCCTGGCCTTTGTCTG A G DMTN Ensembl:ENSG00000158856 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22070145..22070378 26863196 MeRIP-seq:(Medium) rs761655391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34908,RMVar_hsa_circ_28452,RMVar_hsa_circ_63604 99264 RMVar_ID_99264 Human_SNP_ID_355633326 m1A Human chr8 - 22073778 22073778 22073778 CAGAGAGCGGGTTTTCCTTCGGATCGGCAATGACTTTTCCATCTCTTCTTTCAAGATCATCTTTC CAGAGAGCGGGTTTTCCTTCGGATCGGCAATGGCTTTTCCATCTCTTCTTTCAAGATCATCTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22073694..22073777 26863196 MeRIP-seq:(Medium) rs746752772 Functional Loss SNV dbSNP153 33..33 33 - - - 99265 RMVar_ID_99265 Human_SNP_ID_355633333 m1A Human chr8 - 22073788 22073788 22073788 TCCGGTCAGGCAGAGAGCGGGTTTTCCTTCGGATCGGCAATGACTTTTCCATCTCTTCTTTCAAG TCCGGTCAGGCAGAGAGCGGGTTTTCCTTCGGGTCGGCAATGACTTTTCCATCTCTTCTTTCAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22073701..22073797 26863196 MeRIP-seq:(Medium) rs1195441031 Functional Loss SNV dbSNP153 33..33 33 - - - 99266 RMVar_ID_99266 Human_SNP_ID_355635868 m1A Human chr8 + 22081827 22081827 22081827 TTGGCTGTCTTGAACAGCTGGAGGGAAGATGCAGGGGTGGGAAGCGGCCAGGCAGAAAGAGCTCC TTGGCTGTCTTGAACAGCTGGAGGGAAGATGCGGGGGTGGGAAGCGGCCAGGCAGAAAGAGCTCC A G DMTN Ensembl:ENSG00000158856 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22081731..22081881 32194978 MeRIP-seq:(Medium) rs1318583431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995943,Human_RBP_ID_9223093 99267 RMVar_ID_99267 Human_SNP_ID_355635951 m1A Human chr8 + 22081991 22081991 22081991 AGCTCAGCCTCCGGCAGGGAGGTCACCCCTCCACTTCAGCTTGCCCTGACCTCCGCTCGCAAACC AGCTCAGCCTCCGGCAGGGAGGTCACCCCTCCGCTTCAGCTTGCCCTGACCTCCGCTCGCAAACC A G DMTN Ensembl:ENSG00000158856 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22081940..22082042 26863196 MeRIP-seq:(Medium) rs1444790118 Functional Loss SNV dbSNP153 33..33 33 - - - 99268 RMVar_ID_99268 Human_SNP_ID_355638676 m1A Human chr8 + 22089233 22089233 22089233 CTAGAGCGCTGCCGCCGCCGCTTTCGCCCGGGAGCCGGGGGCCGGGCGCCATCATGCTGAGCCGG CTAGAGCGCTGCCGCCGCCGCTTTCGCCCGGGCGCCGGGGGCCGGGCGCCATCATGCTGAGCCGG A C FAM160B2 Ensembl:ENSG00000158863 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:22089184..22089351;chr8:22089196..22089365 26863196 MeRIP-seq:(Medium) rs1181838436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995363,Human_RBP_ID_5243690,Human_RBP_ID_9338187,Human_RBP_ID_18426669 Human_Splice_Rec_955713,Human_Splice_Rec_955745,Human_Splice_Rec_955749,Human_Splice_Rec_955761,Human_Splice_Rec_955763 99269 RMVar_ID_99269 Human_SNP_ID_355638798 m1A Human chr8 - 22089468 22089468 22089468 GTCTGGGAGCGGGACTGGGAAGAGCGAGGGGAAGCGGGGCGCGGCCGGGGAGGCAGAGGAAGGGG GTCTGGGAGCGGGACTGGGAAGAGCGAGGGGATGCGGGGCGCGGCCGGGGAGGCAGAGGAAGGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22089452..22089560 26863196 MeRIP-seq:(Medium) rs12547987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27161969 99270 RMVar_ID_99270 Human_SNP_ID_355638799 m1A Human chr8 - 22089468 22089468 22089468 GTCTGGGAGCGGGACTGGGAAGAGCGAGGGGAAGCGGGGCGCGGCCGGGGAGGCAGAGGAAGGGG GTCTGGGAGCGGGACTGGGAAGAGCGAGGGGAGGCGGGGCGCGGCCGGGGAGGCAGAGGAAGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22089452..22089560 26863196 MeRIP-seq:(Medium) rs12547987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27161969 99271 RMVar_ID_99271 Human_SNP_ID_355640486 m1A Human chr8 + 22094491 22094491 22094491 TGCTGCAGGCCTTCGTGGAGCACTGGAAGGGCATCACGCACTACTACATCGAGAGCACAGGTGCG TGCTGCAGGCCTTCGTGGAGCACTGGAAGGGCGTCACGCACTACTACATCGAGAGCACAGGTGCG A G FAM160B2 Ensembl:ENSG00000158863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22094408..22094565 26863196 MeRIP-seq:(Medium) rs1273777620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845868,Human_RBP_ID_9406059,Human_RBP_ID_18894770 Human_Splice_Rec_955714,Human_Splice_Rec_955715,Human_Splice_Rec_955746,Human_Splice_Rec_955747,Human_Splice_Rec_955752,Human_Splice_Rec_955753,Human_Splice_Rec_955762,Human_Splice_Rec_955764,Human_Splice_Rec_955765 RMVar_hsa_circ_4465,RMVar_hsa_circ_314440,RMVar_hsa_circ_375862,RMVar_hsa_circ_370620,RMVar_hsa_circ_76316,RMVar_hsa_circ_250672,RMVar_hsa_circ_250673,RMVar_hsa_circ_250674 99272 RMVar_ID_99272 Human_SNP_ID_355640597 m1A Human chr8 + 22094803 22094803 22094803 TTGGGGGTCTCACTGGCCTGACTCTGCAAGGAAGAGGTGGCTGCACTTCCCCCAGCTTCCAGCTC TTGGGGGTCTCACTGGCCTGACTCTGCAAGGAGGAGGTGGCTGCACTTCCCCCAGCTTCCAGCTC A G FAM160B2 Ensembl:ENSG00000158863 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22094753..22094854 32194978 MeRIP-seq:(Medium) rs182662840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4465,RMVar_hsa_circ_314440,RMVar_hsa_circ_375862,RMVar_hsa_circ_370620,RMVar_hsa_circ_76316,RMVar_hsa_circ_250672,RMVar_hsa_circ_250673,RMVar_hsa_circ_250674 99273 RMVar_ID_99273 Human_SNP_ID_355641128 m1A Human chr8 + 22096536 22096536 22096536 GCCGAGGTGGGAGGCCCTCTGCGCGCTGGGCCAGGCCGAGGTGGGAGGCCTCTGCGCGCTTGGCC GCCGAGGTGGGAGGCCCTCTGCGCGCTGGGCCCGGCCGAGGTGGGAGGCCTCTGCGCGCTTGGCC A C FAM160B2 Ensembl:ENSG00000158863 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22096513..22096648 26863196 MeRIP-seq:(Medium) rs751646825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958872,Human_RBP_ID_5223539,Human_RBP_ID_19021799,Human_RBP_ID_19139959 RMVar_hsa_circ_3448,RMVar_hsa_circ_4465,RMVar_hsa_circ_375862,RMVar_hsa_circ_370620,RMVar_hsa_circ_76316,RMVar_hsa_circ_250672,RMVar_hsa_circ_250673,RMVar_hsa_circ_250674,RMVar_hsa_circ_107628,RMVar_hsa_circ_250675 99274 RMVar_ID_99274 Human_SNP_ID_355641129 m1A Human chr8 + 22096536 22096536 22096536 GCCGAGGTGGGAGGCCCTCTGCGCGCTGGGCCAGGCCGAGGTGGGAGGCCTCTGCGCGCTTGGCC GCCGAGGTGGGAGGCCCTCTGCGCGCTGGGCCGGGCCGAGGTGGGAGGCCTCTGCGCGCTTGGCC A G FAM160B2 Ensembl:ENSG00000158863 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22096513..22096648 26863196 MeRIP-seq:(Medium) rs751646825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958872,Human_RBP_ID_5223539,Human_RBP_ID_19021799,Human_RBP_ID_19139959 RMVar_hsa_circ_3448,RMVar_hsa_circ_4465,RMVar_hsa_circ_375862,RMVar_hsa_circ_370620,RMVar_hsa_circ_76316,RMVar_hsa_circ_250672,RMVar_hsa_circ_250673,RMVar_hsa_circ_250674,RMVar_hsa_circ_107628,RMVar_hsa_circ_250675 99275 RMVar_ID_99275 Human_SNP_ID_355642430 m1A Human chr8 - 22099778 22099778 22099778 CTGTGCCCAGGAGGAAAGCCACGGCCTCCCGCAGCAGCGCAGGGGAGCGAAGCTGGCGCAGCATG CTGTGCCCAGGAGGAAAGCCACGGCCTCCCGCGGCAGCGCAGGGGAGCGAAGCTGGCGCAGCATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22099729..22099812 26863196 MeRIP-seq:(Medium) rs1348783033 Functional Loss SNV dbSNP153 33..33 33 - - - 99276 RMVar_ID_99276 Human_SNP_ID_355642431 m1A Human chr8 - 22099778 22099778 22099778 CTGTGCCCAGGAGGAAAGCCACGGCCTCCCGCAGCAGCGCAGGGGAGCGAAGCTGGCGCAGCATG CTGTGCCCAGGAGGAAAGCCACGGCCTCCCGCCGCAGCGCAGGGGAGCGAAGCTGGCGCAGCATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22099729..22099812 26863196 MeRIP-seq:(Medium) rs1348783033 Functional Loss SNV dbSNP153 33..33 33 - - - 99277 RMVar_ID_99277 Human_SNP_ID_355642770 m1A Human chr8 - 22100741 22100741 22100741 TGGGCTGAGTCCAAAGGGCGCCGGTTTCACTTACAGGGTGTCCTCATAGCTCTCAGGCTCTGGTG TGGGCTGAGTCCAAAGGGCGCCGGTTTCACTTCCAGGGTGTCCTCATAGCTCTCAGGCTCTGGTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22100693..22100997 32194978 MeRIP-seq:(Medium) rs1051806158 Functional Loss SNV dbSNP153 33..33 33 - - - 99278 RMVar_ID_99278 Human_SNP_ID_355643237 m1A Human chr8 - 22101853 22101853 22101853 CCTGGAGTTCTCCTGGCCCAGGCCCACTAGCTACCTGATCCAGAATCCGGGACATGCGGTCAAAC CCTGGAGTTCTCCTGGCCCAGGCCCACTAGCTGCCTGATCCAGAATCCGGGACATGCGGTCAAAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22101829..22101930 32194978 MeRIP-seq:(Medium) rs199734189 Functional Loss SNV dbSNP153 33..33 33 - - - 99279 RMVar_ID_99279 Human_SNP_ID_355645428 m1A Human chr8 + 22107894 22107894 22107894 GCATCGGCCTCCTTGGAAGTCTTGAGAATTCCACCTGGGGGAGATGTGGGGGATGGGGCAGGGAG GCATCGGCCTCCTTGGAAGTCTTGAGAATTCCGCCTGGGGGAGATGTGGGGGATGGGGCAGGGAG A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22107748..22107993 32194978 MeRIP-seq:(Medium) rs1327319151 Functional Loss SNV dbSNP153 33..33 33 - - - 99280 RMVar_ID_99280 Human_SNP_ID_355645572 m1A Human chr8 - 22108269 22108269 22108269 TCGTGGTACCTGCCTGCGGGGAGAATGGAGCCAGGGGAGACCATCGTGGAGGCGCTGCAGCGGGA TCGTGGTACCTGCCTGCGGGGAGAATGGAGCCCGGGGAGACCATCGTGGAGGCGCTGCAGCGGGA T G NUDT18 Ensembl:ENSG00000275074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22108157..22108347 26863196 MeRIP-seq:(Medium) rs200119438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021809 Human_Splice_Rec_955822,Human_Splice_Rec_955824 RMVar_hsa_circ_8858,RMVar_hsa_circ_92227,RMVar_hsa_circ_250692 99281 RMVar_ID_99281 Human_SNP_ID_355647920 m1A Human chr8 - 22115344 22115344 22115344 GGGGAAACTTGGGAATCATTCTGGCTTAAACAACACCTCCTCCTGCTGCTCACTCCCGCTGAGCC GGGGAAACTTGGGAATCATTCTGGCTTAAACATCACCTCCTCCTGCTGCTCACTCCCGCTGAGCC T A HR Ensembl:ENSG00000168453 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22115293..22115737 26863196 MeRIP-seq:(Medium) rs751048614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27537342 Human_miRNA_ID_848149 99282 RMVar_ID_99282 Human_SNP_ID_355647921 m1A Human chr8 - 22115344 22115344 22115344 GGGGAAACTTGGGAATCATTCTGGCTTAAACAACACCTCCTCCTGCTGCTCACTCCCGCTGAGCC GGGGAAACTTGGGAATCATTCTGGCTTAAACACCACCTCCTCCTGCTGCTCACTCCCGCTGAGCC T G HR Ensembl:ENSG00000168453 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22115293..22115737 26863196 MeRIP-seq:(Medium) rs751048614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27537342 Human_miRNA_ID_848149 99283 RMVar_ID_99283 Human_SNP_ID_355648497 m1A Human chr8 - 22117114 22117114 22117114 CTTCGGCTCTTTTCTCCACCCCTGGCCTCTGGAAAGTCCATGCCCCATCCTCCTGCAGCCCTGCC CTTCGGCTCTTTTCTCCACCCCTGGCCTCTGGGAAGTCCATGCCCCATCCTCCTGCAGCCCTGCC T C HR Ensembl:ENSG00000168453 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22117112..22117195 26863196 MeRIP-seq:(Medium) rs898096199 Functional Loss SNV dbSNP153 33..33 33 - - - 99284 RMVar_ID_99284 Human_SNP_ID_355648555 m1A Human chr8 - 22117351 22117351 22117351 CCCTCGGATTTGCAGAAAGGGGTACCATTGAGAGAGGGAGGAGAGGGGCCGAGGTCACAGAGGCT CCCTCGGATTTGCAGAAAGGGGTACCATTGAGGGAGGGAGGAGAGGGGCCGAGGTCACAGAGGCT T C HR Ensembl:ENSG00000168453 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22117345..22117423 26863196 MeRIP-seq:(Medium) rs1256467505 Functional Loss SNV dbSNP153 33..33 33 - - - 99285 RMVar_ID_99285 Human_SNP_ID_355648956 m1A Human chr8 - 22118840 22118840 22118840 TCCCATGTGCTCGCTCCCTGCCCCACGCCCTCAGGTGAGCTGCACAGACCCAACTCGCACAGACA TCCCATGTGCTCGCTCCCTGCCCCACGCCCTCTGGTGAGCTGCACAGACCCAACTCGCACAGACA T A HR Ensembl:ENSG00000168453 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22118835..22118960 26863196 MeRIP-seq:(Medium) rs1009815725 Functional Loss SNV dbSNP153 33..33 33 - - - 99286 RMVar_ID_99286 Human_SNP_ID_355651782 m1A Human chr8 - 22127086 22127086 22127086 GGGGCTGGGGGTTGGCAGGAGGTGCGGGACACATCGATAGGGAACAAGGATGTGGACTCGGGACA GGGGCTGGGGGTTGGCAGGAGGTGCGGGACACTTCGATAGGGAACAAGGATGTGGACTCGGGACA T A HR Ensembl:ENSG00000168453 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22127023..22127203 26863196 MeRIP-seq:(Medium) rs762346786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_955831,Human_Splice_Rec_955867 99287 RMVar_ID_99287 Human_SNP_ID_355651783 m1A Human chr8 - 22127086 22127086 22127086 GGGGCTGGGGGTTGGCAGGAGGTGCGGGACACATCGATAGGGAACAAGGATGTGGACTCGGGACA GGGGCTGGGGGTTGGCAGGAGGTGCGGGACACGTCGATAGGGAACAAGGATGTGGACTCGGGACA T C HR Ensembl:ENSG00000168453 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22127023..22127203 26863196 MeRIP-seq:(Medium) rs762346786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_955831,Human_Splice_Rec_955867 99288 RMVar_ID_99288 Human_SNP_ID_355651911 m1A Human chr8 + 22127346 22127346 22127346 GTGGTGGCTGGGGGGACAGGCCCTGGGGCCAGAGGCCTTGTTCACTTCCTCGCTGGGTTCGCTGG GTGGTGGCTGGGGGGACAGGCCCTGGGGCCAGGGGCCTTGTTCACTTCCTCGCTGGGTTCGCTGG A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22127299..22127385 26863196 MeRIP-seq:(Medium) rs761593479 Functional Loss SNV dbSNP153 33..33 33 - - - 99289 RMVar_ID_99289 Human_SNP_ID_355653106 m1A Human chr8 - 22130954 22130954 22130954 CAGAGGTCCTGCTGCGCTCTCCGCCGCGCTCTACCTCCATTAGCCGCGCTGCGCGGTGCTGCGCC CAGAGGTCCTGCTGCGCTCTCCGCCGCGCTCTGCCTCCATTAGCCGCGCTGCGCGGTGCTGCGCC T C HR Ensembl:ENSG00000168453 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:22130526..22131050 26863196 MeRIP-seq:(Medium) rs1487387777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_955926 99290 RMVar_ID_99290 Human_SNP_ID_355655226 m1A Human chr8 - 22138266 22138266 22138266 TACCAAAGCAGGCTGGGCCCAGGGTTCTATTTATTGCCTTGCTCTGCCCTCTCCCTTCCCCGGTT TACCAAAGCAGGCTGGGCCCAGGGTTCTATTTGTTGCCTTGCTCTGCCCTCTCCCTTCCCCGGTT T C REEP4 Ensembl:ENSG00000168476 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22138216..22138904 32194978 MeRIP-seq:(Medium) rs1484660551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_697118,Human_RBP_ID_4999385,Human_RBP_ID_17317496,Human_RBP_ID_17666083,Human_RBP_ID_18115509,Human_RBP_ID_18452432,Human_RBP_ID_24252887,Human_RBP_ID_26558460,Human_RBP_ID_27537361 Human_miRNA_ID_825119,Human_miRNA_ID_2349891 RMVar_hsa_circ_76069,RMVar_hsa_circ_250695 99291 RMVar_ID_99291 Human_SNP_ID_355655317 m1A Human chr8 - 22138476 22138476 22138476 GCCCTCAGACGTGGACAGCTAGGGTCTGCTGCATCTGCCCCCTTCTTACCTCGTGCCCTGCAGGG GCCCTCAGACGTGGACAGCTAGGGTCTGCTGCGTCTGCCCCCTTCTTACCTCGTGCCCTGCAGGG T C REEP4 Ensembl:ENSG00000168476 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22138427..22138548 26863196 MeRIP-seq:(Medium) rs753161492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_697123,Human_RBP_ID_1694943,Human_RBP_ID_5123844,Human_RBP_ID_5154228,Human_RBP_ID_7823588,Human_RBP_ID_17665935,Human_RBP_ID_18115511,Human_RBP_ID_22516869,Human_RBP_ID_24252890 Human_Splice_Rec_955938,Human_Splice_Rec_955952,Human_Splice_Rec_955964 Human_miRNA_ID_2384400 RMVar_hsa_circ_76069,RMVar_hsa_circ_250695 99292 RMVar_ID_99292 Human_SNP_ID_355655432 m1A Human chr8 - 22138698 22138698 22138698 CAGTCCCCCGGGCGCCAGCCCGGCCCCGAGAGAAGCCCCTAATCCGCAGCCAGAGCCTGCGTGTG CAGTCCCCCGGGCGCCAGCCCGGCCCCGAGAGGAGCCCCTAATCCGCAGCCAGAGCCTGCGTGTG T C REEP4 Ensembl:ENSG00000168476 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:22138511..22138746 26863410 MeRIP-seq:(Medium) rs982370585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123451,Human_RBP_ID_22775971 Human_Splice_Rec_955936,Human_Splice_Rec_955937,Human_Splice_Rec_955950,Human_Splice_Rec_955951 Human_miRNA_ID_2331385,Human_miRNA_ID_3117213 RMVar_hsa_circ_76069,RMVar_hsa_circ_250695 99293 RMVar_ID_99293 Human_SNP_ID_355656611 m1A Human chr8 - 22141885 22141882 22141886 GTTGGGCAGCACTCGGTTCCGTGCAACTTTCAAGTGAGTTGCGAACTCCGCCCTGTAGGCCGGTG GTTGGGCAGCACTCGGTTCCGTGCAACTTTC____GAGTTGCGAACTCCGCCCTGTAGGCCGGTG CACTT C REEP4 Ensembl:ENSG00000168476 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1193346174 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_4995365,Human_RBP_ID_18426798 99294 RMVar_ID_99294 Human_SNP_ID_355663843 m1A Human chr8 + 22165215 22165215 22165215 AAGGAAAGGGAGAGGGAGACGGCTGGAGCCCGAGGACGAGCGCGGAGCCGCGGACCGAGCGGGGG AAGGAAAGGGAGAGGGAGACGGCTGGAGCCCGCGGACGAGCGCGGAGCCGCGGACCGAGCGGGGG A C BMP1 Ensembl:ENSG00000168487 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr8:22165151..22165575;chr8:22165175..22165321 26863196 MeRIP-seq:(Medium) rs1252503528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3887829,Human_RBP_ID_3972958,Human_RBP_ID_4994937,Human_RBP_ID_5154019,Human_RBP_ID_5404807,Human_RBP_ID_5628943,Human_RBP_ID_9441085 99295 RMVar_ID_99295 Human_SNP_ID_355680025 m1A Human chr8 - 22220188 22220188 22220188 AGGTCACGAGGGTGGACTCCCTACAATCAACAAAGCAAACAGAGAGCCTGTGGGAGGGGCTGACA AGGTCACGAGGGTGGACTCCCTACAATCAACAGAGCAAACAGAGAGCCTGTGGGAGGGGCTGACA T C PHYHIP Ensembl:ENSG00000168490 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:22220138..22220300 26863196 MeRIP-seq:(Medium) rs1248135150 Functional Loss SNV dbSNP153 33..33 33 - - - 99296 RMVar_ID_99296 Human_SNP_ID_355687498 m1A Human chr8 - 22245592 22245592 22245592 CGTTGGGTACCTTCTTGACTCCCCCGAGGGTGAGGTCCCTGGAACGGATGGAGGGAAGGCGGCCG CGTTGGGTACCTTCTTGACTCCCCCGAGGGTGTGGTCCCTGGAACGGATGGAGGGAAGGCGGCCG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22245451..22247961 32194978 MeRIP-seq:(Medium) rs1481364294 Functional Loss SNV dbSNP153 33..33 33 - - - 99297 RMVar_ID_99297 Human_SNP_ID_355688669 m1A Human chr8 + 22249206 22249206 22249206 GGAAGAGGAACTGCTGTTTCTGCAGCTGCCAGACACCCTCCCTGGCCAGCCACCCACCCAGGACA GGAAGAGGAACTGCTGTTTCTGCAGCTGCCAGCCACCCTCCCTGGCCAGCCACCCACCCAGGACA A C POLR3D Ensembl:ENSG00000168495 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22249049..22250113 32194978 MeRIP-seq:(Medium) rs1031790262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960438,Human_RBP_ID_18115530,Human_RBP_ID_26359671,Human_RBP_ID_27831727 Human_miRNA_ID_2029105,Human_miRNA_ID_2689617,Human_miRNA_ID_2692846 RMVar_hsa_circ_18630,RMVar_hsa_circ_103036,RMVar_hsa_circ_103979,RMVar_hsa_circ_250707,RMVar_hsa_circ_126357,RMVar_hsa_circ_49915,RMVar_hsa_circ_250708,RMVar_hsa_circ_330804,RMVar_hsa_circ_250709,RMVar_hsa_circ_83538,RMVar_hsa_circ_114601,RMVar_hsa_circ_250710,RMVar_hsa_circ_250711,RMVar_hsa_circ_80927,RMVar_hsa_circ_250712,RMVar_hsa_circ_250714 99298 RMVar_ID_99298 Human_SNP_ID_355689219 m1A Human chr8 - 22250858 22250858 22250858 AAGCTGCAGTCCACACGCTTCCTGCCCCTGCAACCCAGCAGGCACCAAGAGAAGCCGGCCCCTTC AAGCTGCAGTCCACACGCTTCCTGCCCCTGCATCCCAGCAGGCACCAAGAGAAGCCGGCCCCTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:22250751..22250900 32194978 MeRIP-seq:(Medium) rs1271523302 Functional Loss SNV dbSNP153 33..33 33 - - - 99299 RMVar_ID_99299 Human_SNP_ID_355689368 m1A Human chr8 + 22251522 22251522 22251522 TACTCATGTATGAGCCGAAGTCATATATTGCTAACAAAAAAACTAAATCCTTCATAAGAGAAGTT TACTCATGTATGAGCCGAAGTCATATATTGCTTACAAAAAAACTAAATCCTTCATAAGAGAAGTT A T POLR3D Ensembl:ENSG00000168495 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:22251471..22251572 32194978 MeRIP-seq:(Medium) rs929514786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17317501,Human_RBP_ID_17714429,Human_RBP_ID_18115549,Human_RBP_ID_23298465,Human_RBP_ID_27775208 Human_miRNA_ID_1376048 99300 RMVar_ID_99300 Human_SNP_ID_355690432 m1A Human chr8 + 22256017 22256017 22256017 CAGGGAGCAGGGGATTCTGGGTGGTGGCGGGCATGTTGCAGCAAGTAGGGTAGGTCTCCTTGAGA CAGGGAGCAGGGGATTCTGGGTGGTGGCGGGCTTGTTGCAGCAAGTAGGGTAGGTCTCCTTGAGA A T RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22255903..22256185 26863196 MeRIP-seq:(Medium) rs1258121485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7823689 99301 RMVar_ID_99301 Human_SNP_ID_355690436 m1A Human chr8 + 22256031 22256031 22256031 TTCTGGGTGGTGGCGGGCATGTTGCAGCAAGTAGGGTAGGTCTCCTTGAGAGGGTATCGTTTGAG TTCTGGGTGGTGGCGGGCATGTTGCAGCAAGTGGGGTAGGTCTCCTTGAGAGGGTATCGTTTGAG A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22255873..22256147 26863196 MeRIP-seq:(Medium) rs904525693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18388867 99302 RMVar_ID_99302 Human_SNP_ID_355690625 m1A Human chr8 + 22256632 22256632 22256632 ACAGTGGATGGCAGTGGCTTGGCCAGGCCGCTAACAGCAGGGGCACTGGGAAGTGATTGGATTCT ACAGTGGATGGCAGTGGCTTGGCCAGGCCGCTGACAGCAGGGGCACTGGGAAGTGATTGGATTCT A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22256581..22256719 26863196 MeRIP-seq:(Medium) rs558433750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7823706 99303 RMVar_ID_99303 Human_SNP_ID_355728531 m1A Human chr8 + 22388399 22388399 22388399 GTGGAGATAGAAACGTGTAGGGATGGAGGGGTAGGACATTTCAGATGCAGCCCAGGGCAAGAGAG GTGGAGATAGAAACGTGTAGGGATGGAGGGGTGGGACATTTCAGATGCAGCCCAGGGCAAGAGAG A G SLC39A14 Ensembl:ENSG00000104635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22388393..22388489 26863196 MeRIP-seq:(Medium) rs1192514195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9440647,Human_RBP_ID_18960802 99304 RMVar_ID_99304 Human_SNP_ID_355728582 m1A Human chr8 + 22388590 22388590 22388590 GGCGGTGATGAAGTGGGGGCAGGAGGTTCTGGAGGGGAGGGGCTGGGTGGCCAGGAGGGAACAGC GGCGGTGATGAAGTGGGGGCAGGAGGTTCTGGGGGGGAGGGGCTGGGTGGCCAGGAGGGAACAGC A G SLC39A14 Ensembl:ENSG00000104635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22388585..22388668 26863196 MeRIP-seq:(Medium) rs1477456155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885752,Human_RBP_ID_5223544,Human_RBP_ID_8221026,Human_RBP_ID_8238797,Human_RBP_ID_9440648,Human_RBP_ID_17173812,Human_RBP_ID_18960803,Human_RBP_ID_21995220,Human_RBP_ID_22732633,Human_RBP_ID_26795362 99305 RMVar_ID_99305 Human_SNP_ID_355737349 m1A Human chr8 - 22419729 22419729 22419729 CTCGGGCTGGCGATCGGGCAGCCCAGGGCCCGACTTCCAGTCCCACAGGCTCTTGGCAGAGCCCT CTCGGGCTGGCGATCGGGCAGCCCAGGGCCCGGCTTCCAGTCCCACAGGCTCTTGGCAGAGCCCT T C lnc-PHYHIP-2,lnc-PHYHIP-2:2,RF00017-4569 RNACentral:URS00008B4657,RNACentral:URS00008B6D11,RNACentral:URS000090668B lincRNA,lincRNA,SRP RNA intron,exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:22416198..22419800 32194978 MeRIP-seq:(Medium) rs986234952 Functional Loss SNV dbSNP153 33..33 33 - - - 99306 RMVar_ID_99306 Human_SNP_ID_355743035 m1A Human chr8 + 22441047 22441047 22441047 CCGGGTCCGCTAGGACAGCGGGGCCGCTGGGAAGTTGTGAGAGCGGCGCTCGGGGGCGCGCTTGC CCGGGTCCGCTAGGACAGCGGGGCCGCTGGGATGTTGTGAGAGCGGCGCTCGGGGGCGCGCTTGC A T PPP3CC Ensembl:ENSG00000120910 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22440998..22441194 26863196 MeRIP-seq:(Medium) rs1027153905 Functional Loss SNV dbSNP153 33..33 33 - - - 99307 RMVar_ID_99307 Human_SNP_ID_355774811 m1A Human chr8 - 22564891 22564891 22564891 CACTGTGCCCATCCAGGTTCCCCCGCCACCCCAGGGACCGGAGCCCCCACCCCCACGCTGCTTCC CACTGTGCCCATCCAGGTTCCCCCGCCACCCCCGGGACCGGAGCCCCCACCCCCACGCTGCTTCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:22564855..22564984 26863196 MeRIP-seq:(Medium) rs1474857179 Functional Loss SNV dbSNP153 33..33 33 - - - 99308 RMVar_ID_99308 Human_SNP_ID_355774922 m1A Human chr8 + 22565278 22565276 22565278 CCCAGCCTCTCCCCGCCCCCAGGTGCTGCTGGAGAGAGAGCTGGCCGAGCTGAGCGCCGAGCTGG CCCAGCCTCTCCCCGCCCCCAGGTGCTGCTG__GAGAGAGCTGGCCGAGCTGAGCGCCGAGCTGG GGA G SORBS3 Ensembl:ENSG00000120896 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22564806..22565406 26863196 MeRIP-seq:(Medium) rs982586609 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9405259,Human_RBP_ID_19022625,Human_RBP_ID_23117138 Human_Splice_Rec_957048,Human_Splice_Rec_957049,Human_Splice_Rec_957088,Human_Splice_Rec_957089,Human_Splice_Rec_957110,Human_Splice_Rec_957111,Human_Splice_Rec_957166,Human_Splice_Rec_957167,Human_Splice_Rec_957170,Human_Splice_Rec_957172,Human_Splice_Rec_957173,Human_Splice_Rec_957180,Human_Splice_Rec_957181,Human_Splice_Rec_957195,Human_Splice_Rec_957199,Human_Splice_Rec_957207 RMVar_hsa_circ_363199 99309 RMVar_ID_99309 Human_SNP_ID_355775145 m1A Human chr8 + 22565854 22565854 22565854 GCAGAGCTCGCCGGCGCCCCGACGGGCCCCGGAGCAGCGGCCCCCGGCCGGGTGAGTGGGAGACG GCAGAGCTCGCCGGCGCCCCGACGGGCCCCGGGGCAGCGGCCCCCGGCCGGGTGAGTGGGAGACG A G SORBS3 Ensembl:ENSG00000120896 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr8:22565815..22565951;chr8:22565726..22565906 26863196,26863410 MeRIP-seq:(Medium) rs1457371622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995368,Human_RBP_ID_19021824 Human_Splice_Rec_957050,Human_Splice_Rec_957051,Human_Splice_Rec_957112,Human_Splice_Rec_957168,Human_Splice_Rec_957182,Human_Splice_Rec_957183,Human_Splice_Rec_957200,Human_Splice_Rec_957201,Human_Splice_Rec_957219,Human_Splice_Rec_957237 RMVar_hsa_circ_363199 99310 RMVar_ID_99310 Human_SNP_ID_355775635 m1A Human chr8 - 22567160 22567160 22567160 TTGTCTCTCCTGCTCACCTCCACATAATTAGCAGGGAAGATGCCCAGGCGGCCGTGGTGCTCTCC TTGTCTCTCCTGCTCACCTCCACATAATTAGCCGGGAAGATGCCCAGGCGGCCGTGGTGCTCTCC T G AC037459.3 Ensembl:ENSG00000254230 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22566337..22574839 32194978 MeRIP-seq:(Medium) rs1476619316 Functional Loss SNV dbSNP153 33..33 33 - - - 99311 RMVar_ID_99311 Human_SNP_ID_355776759 m1A Human chr8 - 22571068 22571068 22571068 CGGGCTGAGCGGGCGGCAGCGGTCAGGCGGGGAGACGTGGGGAGCTGGGGGCCGTCGTCACAGAG CGGGCTGAGCGGGCGGCAGCGGTCAGGCGGGGGGACGTGGGGAGCTGGGGGCCGTCGTCACAGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22570880..22571225 26863196 MeRIP-seq:(Medium) rs1274998545 Functional Loss SNV dbSNP153 33..33 33 - - - 99312 RMVar_ID_99312 Human_SNP_ID_355776791 m1A Human chr8 - 22571124 22571124 22571124 CCCCCAAGTCGATGGGGTCAGCTGGGCTGCGCAGGGCTGAGGGGGAGCTGGGGTGACGGGCTGAG CCCCCAAGTCGATGGGGTCAGCTGGGCTGCGCGGGGCTGAGGGGGAGCTGGGGTGACGGGCTGAG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:22571024..22571174 26863196 MeRIP-seq:(Medium) rs1396929017 Functional Loss SNV dbSNP153 33..33 33 - - - 99313 RMVar_ID_99313 Human_SNP_ID_355777972 m1A Human chr8 - 22574835 22574835 22574835 AAAGGCTGCGGGGGTCGTCTGCAGATGCTGGGAGCTCAGGTCCTGGGGAAGGAGGATGTGGGCGG AAAGGCTGCGGGGGTCGTCTGCAGATGCTGGGGGCTCAGGTCCTGGGGAAGGAGGATGTGGGCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22574720..22575116 26863196 MeRIP-seq:(Medium) rs546826080 Functional Loss SNV dbSNP153 33..33 33 - - - 99314 RMVar_ID_99314 Human_SNP_ID_355781273 m1A Human chr8 - 22585068 22585068 22585068 GCCGGCCCTCGGGCTGAGGGAGGTTGGGCTGGAGTAGGAGGACCTTAAGGAGGACTGACTCTCAG GCCGGCCCTCGGGCTGAGGGAGGTTGGGCTGGGGTAGGAGGACCTTAAGGAGGACTGACTCTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22585018..22585107 26863196 MeRIP-seq:(Medium) rs763539020 Functional Loss SNV dbSNP153 33..33 33 - - - 99315 RMVar_ID_99315 Human_SNP_ID_355781370 m1A Human chr8 + 22585299 22585299 22585299 CCCTGGGCAGGCTGGGGGTGGCCCTGGCACACACTGTCCCTTTCCCACTTTCAGCTTCCAGAGTC CCCTGGGCAGGCTGGGGGTGGCCCTGGCACACGCTGTCCCTTTCCCACTTTCAGCTTCCAGAGTC A G PDLIM2 Ensembl:ENSG00000120913 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22585297..22585405 26863196 MeRIP-seq:(Medium) rs1464439733 Functional Loss SNV dbSNP153 33..33 33 - - - 99316 RMVar_ID_99316 Human_SNP_ID_355782620 m1A Human chr8 - 22589345 22589345 22589345 TACCTGGGCCTGGAGGAACGAGGGCCCGGGGAAGGCGGCAGCACCAGCACCGCCGAGTCGCCAGC TACCTGGGCCTGGAGGAACGAGGGCCCGGGGAGGGCGGCAGCACCAGCACCGCCGAGTCGCCAGC T C lnc-BIN3-2 RNACentral:URS00008BCC24 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:22589301..22593825 26863196 MeRIP-seq:(Medium) rs917372180 Functional Loss SNV dbSNP153 33..33 33 - - - 99317 RMVar_ID_99317 Human_SNP_ID_355782632 m1A Human chr8 + 22589373 22589373 22589373 CGCCTTCCCCGGGCCCTCGTTCCTCCAGGCCCAGGTACCAGCAGGCCCCGGAGGGTCGGGTTGGG CGCCTTCCCCGGGCCCTCGTTCCTCCAGGCCCGGGTACCAGCAGGCCCCGGAGGGTCGGGTTGGG A G PDLIM2,AC037459.1 Ensembl:ENSG00000120913,Ensembl:ENSG00000248235 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22589323..22593767 26863196 MeRIP-seq:(Medium) rs1304347201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958905,Human_RBP_ID_4994944,Human_RBP_ID_17666088 Human_Splice_Rec_957292,Human_Splice_Rec_957293,Human_Splice_Rec_957306,Human_Splice_Rec_957307,Human_Splice_Rec_957324,Human_Splice_Rec_957325,Human_Splice_Rec_957342,Human_Splice_Rec_957343,Human_Splice_Rec_957356,Human_Splice_Rec_957357,Human_Splice_Rec_957374,Human_Splice_Rec_957375,Human_Splice_Rec_957417,Human_Splice_Rec_957432,Human_Splice_Rec_957433,Human_Splice_Rec_957446,Human_Splice_Rec_957447,Human_Splice_Rec_957464,Human_Splice_Rec_957465,Human_Splice_Rec_957482,Human_Splice_Rec_957483,Human_Splice_Rec_957499,Human_Splice_Rec_957505,Human_Splice_Rec_957511,Human_Splice_Rec_957515,Human_Splice_Rec_957523,Human_Splice_Rec_957531 99318 RMVar_ID_99318 Human_SNP_ID_355786508 m1A Human chr8 + 22600932 22600932 22600932 TGGCACGGGGCTGCATAGTGCCTGGAGTCACCAGCACCTACAGACGGATCCCCGACGCTGCCCAC TGGCACGGGGCTGCATAGTGCCTGGAGTCACCGGCACCTACAGACGGATCCCCGACGCTGCCCAC A G C8orf58,AC037459.1 Ensembl:ENSG00000241852,Ensembl:ENSG00000248235 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22600857..22600966 26863196 MeRIP-seq:(Medium) rs780673336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_957518,Human_Splice_Rec_957530,Human_Splice_Rec_957536,Human_Splice_Rec_957538,Human_Splice_Rec_957550,Human_Splice_Rec_957562,Human_Splice_Rec_957572 99319 RMVar_ID_99319 Human_SNP_ID_355786522 m1A Human chr8 + 22600954 22600952 22600954 TGGAGTCACCAGCACCTACAGACGGATCCCCGACGCTGCCCACGGGTGCTCATCCTGGGAGAGAG TGGAGTCACCAGCACCTACAGACGGATCCCC__CGCTGCCCACGGGTGCTCATCCTGGGAGAGAG CGA C C8orf58,AC037459.1 Ensembl:ENSG00000241852,Ensembl:ENSG00000248235 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22600839..22601064 26863196 MeRIP-seq:(Medium) rs1305991483 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_957518,Human_Splice_Rec_957530,Human_Splice_Rec_957536,Human_Splice_Rec_957538,Human_Splice_Rec_957550,Human_Splice_Rec_957562,Human_Splice_Rec_957572 99320 RMVar_ID_99320 Human_SNP_ID_355786542 m1A Human chr8 + 22600981 22600981 22600981 CCCCGACGCTGCCCACGGGTGCTCATCCTGGGAGAGAGGTGACAAGTTCAGAGGTGTCGGCAGGG CCCCGACGCTGCCCACGGGTGCTCATCCTGGGGGAGAGGTGACAAGTTCAGAGGTGTCGGCAGGG A G C8orf58,AC037459.1 Ensembl:ENSG00000241852,Ensembl:ENSG00000248235 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22600930..22601002 26863196 MeRIP-seq:(Medium) rs1475542130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_957518,Human_Splice_Rec_957530,Human_Splice_Rec_957536,Human_Splice_Rec_957538,Human_Splice_Rec_957550,Human_Splice_Rec_957562,Human_Splice_Rec_957572 99321 RMVar_ID_99321 Human_SNP_ID_355788062 m1A Human chr8 + 22604841 22604841 22604841 TTTGTCCCCCCGGTGTCGCTGCCCTGGCCCGCAGGTGGGTTGGGGGGCCCCCTGCCGCCCCTCTG TTTGTCCCCCCGGTGTCGCTGCCCTGGCCCGCGGGTGGGTTGGGGGGCCCCCTGCCGCCCCTCTG A G CCAR2 Ensembl:ENSG00000158941 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22604808..22604881 26863196 MeRIP-seq:(Medium) rs1231324622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995370,Human_RBP_ID_19140891,Human_RBP_ID_22114841 Human_Splice_Rec_957589,Human_Splice_Rec_957627,Human_Splice_Rec_957637 RMVar_hsa_circ_128193,RMVar_hsa_circ_250749,RMVar_hsa_circ_92250,RMVar_hsa_circ_250748 99322 RMVar_ID_99322 Human_SNP_ID_355791806 m1A Human chr8 - 22614977 22614977 22614977 CCACTCACCACTTGGTACAGCCGCTCAAATCAATGCCAGTCTGGGCCTGCGCACAGCGGATGGCG CCACTCACCACTTGGTACAGCCGCTCAAATCAGTGCCAGTCTGGGCCTGCGCACAGCGGATGGCG T C AC037459.2 Ensembl:ENSG00000253200 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:22614926..22615000 32194978 MeRIP-seq:(Medium) rs199504395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27537477 99323 RMVar_ID_99323 Human_SNP_ID_355792413 m1A Human chr8 + 22616178 22616176 22616179 AGAAGCCACCAAGGAGGAAGAAGCCATCAAAGAGGAGGTGGTCAAGGAGCCCAAGGATGAGGCAC AGAAGCCACCAAGGAGGAAGAAGCCATCAAA___GAGGTGGTCAAGGAGCCCAAGGATGAGGCAC AGAG A CCAR2 Ensembl:ENSG00000158941 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22616067..22616250 26863196 MeRIP-seq:(Medium) rs761148208 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_845055,Human_RBP_ID_3973703,Human_RBP_ID_8918166 Human_Splice_Rec_957613,Human_Splice_Rec_957667,Human_Splice_Rec_957721,Human_Splice_Rec_957749 RMVar_hsa_circ_1040,RMVar_hsa_circ_13949,RMVar_hsa_circ_11191,RMVar_hsa_circ_85739,RMVar_hsa_circ_250757 99324 RMVar_ID_99324 Human_SNP_ID_355793843 m1A Human chr8 + 22619248 22619248 22619248 AGCTGCGAGTCCGGCTGGCGGAGGCCGAGGAGACCGCCCGGACGGCGGAGCGACAGAAGAGCCAG AGCTGCGAGTCCGGCTGGCGGAGGCCGAGGAGGCCGCCCGGACGGCGGAGCGACAGAAGAGCCAG A G CCAR2 Ensembl:ENSG00000158941 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22619201..22619350 26863196 MeRIP-seq:(Medium) rs765189898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4979106,Human_RBP_ID_8922888,Human_RBP_ID_23088080 Human_Splice_Rec_957624,Human_Splice_Rec_957678,Human_Splice_Rec_957732,Human_Splice_Rec_957760,Human_Splice_Rec_957774,Human_Splice_Rec_957782,Human_Splice_Rec_957790 RMVar_hsa_circ_13949,RMVar_hsa_circ_85739,RMVar_hsa_circ_250757,RMVar_hsa_circ_90912,RMVar_hsa_circ_250761 99325 RMVar_ID_99325 Human_SNP_ID_355809302 m1A Human chr8 - 22668943 22668943 22668943 TGCCGCGTCCCGGCTCCCTCCGGTCCCGCGCGACCCCTCCGCCCCAGAGCAAGGCCCGACAGCCC TGCCGCGTCCCGGCTCCCTCCGGTCCCGCGCGTCCCCTCCGCCCCAGAGCAAGGCCCGACAGCCC T A BIN3 Ensembl:ENSG00000147439 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:22668940..22669078 26863196 MeRIP-seq:(Medium) rs1261121138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26765911 99326 RMVar_ID_99326 Human_SNP_ID_355815819 m1A Human chr8 + 22693367 22693346 22693367 CCCCCCGATCTGCCACCGCCACCGCCACCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CCCCCCGATCTG_____________________CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC GCCACCGCCACCGCCACCGCCA G AC055854.1 Ensembl:ENSG00000253125 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr8:22693315..22693429;chr8:22693272..22693463;chr8:22693317..22693398 26863196 MeRIP-seq:(Medium) rs1354650402 Functional Loss DEL dbSNP153 13..33 33 - - - 99327 RMVar_ID_99327 Human_SNP_ID_355815835 m1A Human chr8 + 22693367 22693364 22693367 CCCCCCGATCTGCCACCGCCACCGCCACCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CCCCCCGATCTGCCACCGCCACCGCCACCG___CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC GCCA G AC055854.1 Ensembl:ENSG00000253125 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr8:22693315..22693429;chr8:22693272..22693463;chr8:22693317..22693398 26863196 MeRIP-seq:(Medium) rs1369697275 Functional Loss DEL dbSNP153 31..33 33 - - - 99328 RMVar_ID_99328 Human_SNP_ID_355815838 m1A Human chr8 + 22693367 22693367 22693367 CCCCCCGATCTGCCACCGCCACCGCCACCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC CCCCCCGATCTGCCACCGCCACCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC A G AC055854.1 Ensembl:ENSG00000253125 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr8:22693315..22693429;chr8:22693272..22693463;chr8:22693317..22693398 26863196 MeRIP-seq:(Medium) rs12335145 Functional Loss SNV dbSNP153 33..33 33 - - - 99329 RMVar_ID_99329 Human_SNP_ID_355893431 m1A Human chr8 - 22988545 22988545 22988545 GTTTCTCTTGATAAATGGATCCTGCTGCCTGAAGGATGGGGAGCTCCCAGAGTTGGGTGGAGCCA GTTTCTCTTGATAAATGGATCCTGCTGCCTGAGGGATGGGGAGCTCCCAGAGTTGGGTGGAGCCA T C PEBP4,AC107959.1 Ensembl:ENSG00000134020,Ensembl:ENSG00000245025 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22988535..22988608 26863196 MeRIP-seq:(Medium) rs1284658828 Functional Loss SNV dbSNP153 33..33 33 - - - 99330 RMVar_ID_99330 Human_SNP_ID_355898172 m1A Human chr8 + 23006947 23006947 23006947 GTGCAGCGGCCTCTGCTGCAGGCACCCTTCCTACCCCCCAAGCCACCGCCCCCGATCATCGTGGT GTGCAGCGGCCTCTGCTGCAGGCACCCTTCCTCCCCCCCAAGCCACCGCCCCCGATCATCGTGGT A C RHOBTB2 Ensembl:ENSG00000008853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23006900..23006987 26863196 MeRIP-seq:(Medium) rs755325607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114199,RMVar_hsa_circ_250766,RMVar_hsa_circ_78383,RMVar_hsa_circ_250765,RMVar_hsa_circ_340998 99331 RMVar_ID_99331 Human_SNP_ID_355898307 m1A Human chr8 + 23007204 23007204 23007204 GGAGCCAGGGGGCACCCACCCAGAGGACCACCAGGGCCACTCTGATCAACACCACCACCATCACC GGAGCCAGGGGGCACCCACCCAGAGGACCACCGGGGCCACTCTGATCAACACCACCACCATCACC A G RHOBTB2 Ensembl:ENSG00000008853 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23007153..23007228 26863196 MeRIP-seq:(Medium) rs1420720154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27537514 RMVar_hsa_circ_114199,RMVar_hsa_circ_250766,RMVar_hsa_circ_78383,RMVar_hsa_circ_250765,RMVar_hsa_circ_340998 99332 RMVar_ID_99332 Human_SNP_ID_355901495 m1A Human chr8 + 23018799 23018799 23018799 TGCAATAGGGGCCAAAAGTCAGGGAAAGGGGCACTGACCTGTAGTGAAAGGCCACAGGACACAGC TGCAATAGGGGCCAAAAGTCAGGGAAAGGGGCCCTGACCTGTAGTGAAAGGCCACAGGACACAGC A C RHOBTB2 Ensembl:ENSG00000008853 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23018749..23018925 26863196 MeRIP-seq:(Medium) rs910044333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18115776 99333 RMVar_ID_99333 Human_SNP_ID_355901521 m1A Human chr8 + 23018895 23018895 23018895 GAGAAGAGGGAGAATGGAGCAGGAGGAAAAGCAGAGTTGGTCTAGAGAGGAGGAGGGCGGGGCTG GAGAAGAGGGAGAATGGAGCAGGAGGAAAAGCGGAGTTGGTCTAGAGAGGAGGAGGGCGGGGCTG A G RHOBTB2 Ensembl:ENSG00000008853 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23018707..23018957 26863196 MeRIP-seq:(Medium) rs1226302523 Functional Loss SNV dbSNP153 33..33 33 - - - 99334 RMVar_ID_99334 Human_SNP_ID_355901813 m1A Human chr8 + 23019677 23019677 23019677 GCAACCTGGGTACCCTGGTGGGGATGCAGGGAAGGCCGGGGCAGAGAAAGTGAAGGTCGACCCAG GCAACCTGGGTACCCTGGTGGGGATGCAGGGAGGGCCGGGGCAGAGAAAGTGAAGGTCGACCCAG A G RHOBTB2 Ensembl:ENSG00000008853 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23019633..23019764 26863196 MeRIP-seq:(Medium) rs1369432543 Functional Loss SNV dbSNP153 33..33 33 - - - 99335 RMVar_ID_99335 Human_SNP_ID_355902565 m1A Human chr8 - 23021574 23021574 23021574 CATAGCCCCCATCTATGGACAGGCTGGGACAGAGGCAGATGGGTTAGATCACACATAACAATAGG CATAGCCCCCATCTATGGACAGGCTGGGACAGGGGCAGATGGGTTAGATCACACATAACAATAGG T C TNFRSF10B Ensembl:ENSG00000120889 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:23021322..23021720 32194978 MeRIP-seq:(Medium) rs752268796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7824374,Human_RBP_ID_8918242,Human_RBP_ID_16393614,Human_RBP_ID_17319979,Human_RBP_ID_18115793,Human_RBP_ID_26558064 RMVar_hsa_circ_85268,RMVar_hsa_circ_250771 99336 RMVar_ID_99336 Human_SNP_ID_355904751 m1A Human chr8 - 23028555 23028555 23028555 GGTCAAGGTCGGTGATTGTACACCCTGGAGTGACATCGAATGTGTCCACAAAGAATCAGGTACAA GGTCAAGGTCGGTGATTGTACACCCTGGAGTGCCATCGAATGTGTCCACAAAGAATCAGGTACAA T G TNFRSF10B Ensembl:ENSG00000120889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:23028309..23029725 32194978 MeRIP-seq:(Medium) rs150063854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88350,Human_RBP_ID_697421,Human_RBP_ID_958416,Human_RBP_ID_1055070,Human_RBP_ID_1695124,Human_RBP_ID_2054215,Human_RBP_ID_3972991,Human_RBP_ID_8918294,Human_RBP_ID_18125201,Human_RBP_ID_18472481,Human_RBP_ID_19021850,Human_RBP_ID_19140914,Human_RBP_ID_22465140,Human_RBP_ID_26358882,Human_RBP_ID_26554793,Human_RBP_ID_27831734 Human_Splice_Rec_958090,Human_Splice_Rec_958106,Human_Splice_Rec_958107,Human_Splice_Rec_958122,Human_Splice_Rec_958123,Human_Splice_Rec_958140,Human_Splice_Rec_958148 Human_miRNA_ID_2953769,Human_miRNA_ID_2953770,Human_miRNA_ID_2957512,Human_miRNA_ID_2957513,Human_miRNA_ID_2996260,Human_miRNA_ID_2996261 RMVar_hsa_circ_250772,RMVar_hsa_circ_279153,RMVar_hsa_circ_250773,RMVar_hsa_circ_112959 99337 RMVar_ID_99337 Human_SNP_ID_355915956 m1A Human chr8 - 23068849 23068849 23068849 GACAGAACGCCCCGGCCGCTTCGGGGGCCCGGAAAAGGCACGGCCCAGGACCCAGGGAGGCGCGG GACAGAACGCCCCGGCCGCTTCGGGGGCCCGGGAAAGGCACGGCCCAGGACCCAGGGAGGCGCGG T C TNFRSF10B Ensembl:ENSG00000120889 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:23068801..23069025 26863196 MeRIP-seq:(Medium) rs1294645091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18452450,Human_RBP_ID_22465142 Human_Splice_Rec_958083,Human_Splice_Rec_958099,Human_Splice_Rec_958117,Human_Splice_Rec_958149 Human_miRNA_ID_2039727,Human_miRNA_ID_3018709 RMVar_hsa_circ_250773,RMVar_hsa_circ_112959 99338 RMVar_ID_99338 Human_SNP_ID_355915980 m1A Human chr8 - 23068887 23068887 23068887 GACTATAAGAGCGTTCCCTACCGCCATGGAACAACGGGGACAGAACGCCCCGGCCGCTTCGGGGG GACTATAAGAGCGTTCCCTACCGCCATGGAACGACGGGGACAGAACGCCCCGGCCGCTTCGGGGG T C TNFRSF10B Ensembl:ENSG00000120889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23068836..23069028 26863196 MeRIP-seq:(Medium) rs1190108568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1695136,Human_RBP_ID_4979464,Human_RBP_ID_8923406,Human_RBP_ID_16393955 RMVar_hsa_circ_250773,RMVar_hsa_circ_112959 99339 RMVar_ID_99339 Human_SNP_ID_355960893 m1A Human chr8 + 23224672 23224672 23224672 ACATGCCCCGCCACAAGTGACCCGGGCCAGGCACCCCCGCCGCGTCCCCCTCTCTCTCTGCCCCC ACATGCCCCGCCACAAGTGACCCGGGCCAGGCCCCCCCGCCGCGTCCCCCTCTCTCTCTGCCCCC A C AC100861.1 Ensembl:ENSG00000246582 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23224662..23224742 26863196 MeRIP-seq:(Medium) rs1039694135 Functional Loss SNV dbSNP153 33..33 33 - - - 99340 RMVar_ID_99340 Human_SNP_ID_355967184 m1A Human chr8 - 23246699 23246699 23246699 GGCTGGGGCCTCGGCCTCCCGCTCCGGGGACCACATCGGAACCCCAGCCCCGGCAAGGCTGCGAA GGCTGGGGCCTCGGCCTCCCGCTCCGGGGACCCCATCGGAACCCCAGCCCCGGCAAGGCTGCGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23246651..23246819 26863196 MeRIP-seq:(Medium) rs1362439177 Functional Loss SNV dbSNP153 33..33 33 - - - 99341 RMVar_ID_99341 Human_SNP_ID_355980076 m1A Human chr8 - 23290042 23290042 23290042 AGGTCAGCCCCCATTCTTCCTGCCTGCGCAGCACCCGGGGCACATACAAAGGCTGGTCAGGCTTG AGGTCAGCCCCCATTCTTCCTGCCTGCGCAGCCCCCGGGGCACATACAAAGGCTGGTCAGGCTTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:23289991..23290092 32194978 MeRIP-seq:(Medium) rs953314508 Functional Loss SNV dbSNP153 33..33 33 - - - 99342 RMVar_ID_99342 Human_SNP_ID_355980148 m1A Human chr8 - 23290240 23290240 23290240 CAGGCCCCAGAGGCTCAGGGCCAACAGGGTCCAGCAGTGGCTCATTCTCACACCTTTGTCCTGGG CAGGCCCCAGAGGCTCAGGGCCAACAGGGTCCGGCAGTGGCTCATTCTCACACCTTTGTCCTGGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:23290190..23290290 32194978 MeRIP-seq:(Medium) rs774597756 Functional Loss SNV dbSNP153 33..33 33 - - - 99343 RMVar_ID_99343 Human_SNP_ID_355980205 m1A Human chr8 - 23290381 23290381 23290381 CCACCTCCTCTTCGTCCTCTTCCTCCTCTGCCACCAGCCTCTTCTCCAACAGACTCTCCTTCCCC CCACCTCCTCTTCGTCCTCTTCCTCCTCTGCCCCCAGCCTCTTCTCCAACAGACTCTCCTTCCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23290262..23290475 26863196 MeRIP-seq:(Medium) rs202214700 Functional Loss SNV dbSNP153 33..33 33 - - - 99344 RMVar_ID_99344 Human_SNP_ID_355980216 m1A Human chr8 + 23290399 23290393 23290400 GGAGAAGAGGCTGGTGGCAGAGGAGGAAGAGGACGAAGAGGAGGTGGAAGAGGATGGCCCCAGCA GGAGAAGAGGCTGGTGGCAGAGGAGGA_______GAAGAGGAGGTGGAAGAGGATGGCCCCAGCA AAGAGGAC A R3HCC1 Ensembl:ENSG00000104679 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23290215..23290483 26863196 MeRIP-seq:(Medium) rs767850453 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_4999729,Human_RBP_ID_8944450,Human_RBP_ID_26162585,Human_RBP_ID_26558071 Human_Splice_Rec_958390,Human_Splice_Rec_958391,Human_Splice_Rec_958407,Human_Splice_Rec_958423,Human_Splice_Rec_958437,Human_Splice_Rec_958451,Human_Splice_Rec_958463 99345 RMVar_ID_99345 Human_SNP_ID_355981686 m1A Human chr8 + 23294823 23294823 23294823 GTTCTCGGTGCTCAAGATCCGGCCCCTCACACAGGGAACCAAGCAGTCAAAGCTCAAAGCCTTGC GTTCTCGGTGCTCAAGATCCGGCCCCTCACACGGGGAACCAAGCAGTCAAAGCTCAAAGCCTTGC A G R3HCC1 Ensembl:ENSG00000104679 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:23293308..23294853 32194978 MeRIP-seq:(Medium) rs1245892046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17317595 Human_Splice_Rec_958396,Human_Splice_Rec_958397,Human_Splice_Rec_958412,Human_Splice_Rec_958413,Human_Splice_Rec_958428,Human_Splice_Rec_958429,Human_Splice_Rec_958442,Human_Splice_Rec_958443,Human_Splice_Rec_958468,Human_Splice_Rec_958469 99346 RMVar_ID_99346 Human_SNP_ID_355982219 m1A Human chr8 - 23296075 23296075 23296075 TCTCCAGGCCTCAGGGCGGCAGCGGACCCCGGACAGCAGGCCGCTCTTTCTTTTTGTGTTGGAGT TCTCCAGGCCTCAGGGCGGCAGCGGACCCCGGCCAGCAGGCCGCTCTTTCTTTTTGTGTTGGAGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr8:23296025..23296166;chr8:23296030..23296130 26863196,32194978 MeRIP-seq:(Medium) rs1243231807 Functional Loss SNV dbSNP153 33..33 33 - - - 99347 RMVar_ID_99347 Human_SNP_ID_355982235 m1A Human chr8 + 23296097 23296097 23296097 CGGCCTGCTGTCCGGGGTCCGCTGCCGCCCTGAGGCCTGGAGACCCAACTGGCCTGGATCTGCGT CGGCCTGCTGTCCGGGGTCCGCTGCCGCCCTGGGGCCTGGAGACCCAACTGGCCTGGATCTGCGT A G R3HCC1 Ensembl:ENSG00000104679 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23296049..23296179 26863196 MeRIP-seq:(Medium) rs1304332094 Functional Loss SNV dbSNP153 33..33 33 - - - 99348 RMVar_ID_99348 Human_SNP_ID_355990115 m1A Human chr8 - 23322182 23322182 23322182 GTTCAATGCCGAGTCTCAGGGCTGCAACCACGAGGAGGATGCTGGTGTGAGATGCAACACCCCTG GTTCAATGCCGAGTCTCAGGGCTGCAACCACGCGGAGGATGCTGGTGTGAGATGCAACACCCCTG T G LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:23322081..23322328;chr8:23322087..23322224 26863196 MeRIP-seq:(Medium) rs780056153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_958482,Human_Splice_Rec_958483,Human_Splice_Rec_958504,Human_Splice_Rec_958505,Human_Splice_Rec_958510,Human_Splice_Rec_958511,Human_Splice_Rec_958514,Human_Splice_Rec_958515,Human_Splice_Rec_958520,Human_Splice_Rec_958521,Human_Splice_Rec_958526 Human_miRNA_ID_2441164,Human_miRNA_ID_2450212 RMVar_hsa_circ_11094,RMVar_hsa_circ_45914,RMVar_hsa_circ_28168,RMVar_hsa_circ_43275,RMVar_hsa_circ_53278,RMVar_hsa_circ_250782,RMVar_hsa_circ_109885,RMVar_hsa_circ_331761,RMVar_hsa_circ_343155,RMVar_hsa_circ_48673,RMVar_hsa_circ_14449,RMVar_hsa_circ_88311,RMVar_hsa_circ_372342,RMVar_hsa_circ_250785,RMVar_hsa_circ_250786 99349 RMVar_ID_99349 Human_SNP_ID_355990162 m1A Human chr8 - 23322283 23322283 23322283 GCTTTCATAGAGCATGTTTATTCTCCCCTTGCAGGGATCGGACCCATCCACCTCAACGAGATCCA GCTTTCATAGAGCATGTTTATTCTCCCCTTGCCGGGATCGGACCCATCCACCTCAACGAGATCCA T G LOXL2 Ensembl:ENSG00000134013 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23322251..23322300 26863196 MeRIP-seq:(Medium) rs1439167340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11094,RMVar_hsa_circ_28168,RMVar_hsa_circ_43275,RMVar_hsa_circ_53278,RMVar_hsa_circ_343155,RMVar_hsa_circ_372342,RMVar_hsa_circ_250786 99350 RMVar_ID_99350 Human_SNP_ID_355991652 m1A Human chr8 - 23328474 23328472 23328475 CAAAAATGGAGAATGGGGGACCGTCTGCGACGACAAGTGGGACCTGGTGTCGGCCAGTGTGGTCT CAAAAATGGAGAATGGGGGACCGTCTGCGAC___AAGTGGGACCTGGTGTCGGCCAGTGTGGTCT TGTC T LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr8:23328345..23328616;chr8:23328376..23328575;chr8:23328451..23328475;chr8:23328399..23328594 26863196 MeRIP-seq:(Medium) rs1397453783 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_958480,Human_Splice_Rec_958481,Human_Splice_Rec_958503,Human_Splice_Rec_958508,Human_Splice_Rec_958509,Human_Splice_Rec_958513,Human_Splice_Rec_958518,Human_Splice_Rec_958519,Human_Splice_Rec_958524,Human_Splice_Rec_958525 RMVar_hsa_circ_11094,RMVar_hsa_circ_28168,RMVar_hsa_circ_43275,RMVar_hsa_circ_53278,RMVar_hsa_circ_343155,RMVar_hsa_circ_372342,RMVar_hsa_circ_250786,RMVar_hsa_circ_319347,RMVar_hsa_circ_340326 99351 RMVar_ID_99351 Human_SNP_ID_355991657 m1A Human chr8 + 23328481 23328481 23328481 ACTGGCCGACACCAGGTCCCACTTGTCGTCGCAGACGGTCCCCCATTCTCCATTTTTGAGCACCT ACTGGCCGACACCAGGTCCCACTTGTCGTCGCCGACGGTCCCCCATTCTCCATTTTTGAGCACCT A C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23328334..23328626 26863196 MeRIP-seq:(Medium) rs748461342 Functional Loss SNV dbSNP153 33..33 33 - - - 99352 RMVar_ID_99352 Human_SNP_ID_355992959 m1A Human chr8 + 23332331 23332331 23332331 ACACTCATACACACCCCCTACACACATACACAACCCCCACATACACCCCCACACTCATACACACC ACACTCATACACACCCCCTACACACATACACACCCCCCACATACACCCCCACACTCATACACACC A C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23332330..23332777 26863196 MeRIP-seq:(Medium) rs1383801036 Functional Loss SNV dbSNP153 33..33 33 - - - 99353 RMVar_ID_99353 Human_SNP_ID_355992984 m1A Human chr8 + 23332376 23332374 23332376 CCCCCACACTCATACACACCCACACACACCCCACATACACACTCATACACACACACTCATACACA CCCCCACACTCATACACACCCACACACACCC__CATACACACTCATACACACACACTCATACACA CCA C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23332374..23332447 26863196 MeRIP-seq:(Medium) rs1461718752 Functional Loss DEL dbSNP153 32..33 33 - - - 99354 RMVar_ID_99354 Human_SNP_ID_355993020 m1A Human chr8 + 23332424 23332422 23332424 ACACACACTCATACACACACCGCCACACACCCACAAACACACCCCACACACTCCTACAGACACAC ACACACACTCATACACACACCGCCACACACC__CAAACACACCCCACACACTCCTACAGACACAC CCA C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:23332307..23332436 26863196 MeRIP-seq:(Medium) rs1231505022 Functional Loss DEL dbSNP153 32..33 33 - - - 99355 RMVar_ID_99355 Human_SNP_ID_355995529 m1A Human chr8 + 23341112 23341112 23341112 CACAGATCTGCTTCCAGGTCTTGCCCTCCTTCACCTCCACGTAGCCCTCCATCACTGGGGTGCGC CACAGATCTGCTTCCAGGTCTTGCCCTCCTTCTCCTCCACGTAGCCCTCCATCACTGGGGTGCGC A T AC090197.1 Ensembl:ENSG00000253837 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:23331990..23370705 32194978 MeRIP-seq:(Medium) rs897164646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_958554,Human_Splice_Rec_958556,Human_Splice_Rec_958557 99356 RMVar_ID_99356 Human_SNP_ID_356003452 m1A Human chr8 + 23368287 23368286 23368287 AATGGGGCCAGCTGTCATACTGTGCCAGGCTCAGGGGGGACAGGAGGGCCAGCATAGCCAGGCAG AATGGGGCCAGCTGTCATACTGTGCCAGGCTC_GGGGGGACAGGAGGGCCAGCATAGCCAGGCAG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23368242..23368368 26863196 MeRIP-seq:(Medium) rs774250858 Functional Loss DEL dbSNP153 33..33 33 - - - 99357 RMVar_ID_99357 Human_SNP_ID_356003453 m1A Human chr8 + 23368287 23368287 23368287 AATGGGGCCAGCTGTCATACTGTGCCAGGCTCAGGGGGGACAGGAGGGCCAGCATAGCCAGGCAG AATGGGGCCAGCTGTCATACTGTGCCAGGCTCTGGGGGGACAGGAGGGCCAGCATAGCCAGGCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23368242..23368368 26863196 MeRIP-seq:(Medium) rs1563203953 Functional Loss SNV dbSNP153 33..33 33 - - - 99358 RMVar_ID_99358 Human_SNP_ID_356013274 m1A Human chr8 - 23403921 23403921 23403921 GTAAGAGCGCTTCCCGCGCCACCCCCTCCCCGAAGCGGTTCGCGAGAAAGCGGGAGCGTCCCTAT GTAAGAGCGCTTCCCGCGCCACCCCCTCCCCGGAGCGGTTCGCGAGAAAGCGGGAGCGTCCCTAT T C LOXL2,ENTPD4 Ensembl:ENSG00000134013,Ensembl:ENSG00000197217 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:23403907..23404049 26863410 MeRIP-seq:(Medium) rs1241009270 Functional Loss SNV dbSNP153 33..33 33 - - - 99359 RMVar_ID_99359 Human_SNP_ID_356013330 m1A Human chr8 + 23404093 23404093 23404093 TGGTCTCCGATGGCTGGAGAAAGCAAGCACCAAGCGTAGGTAGCCGCGCGCTGGAGTCGCGCGTT TGGTCTCCGATGGCTGGAGAAAGCAAGCACCAGGCGTAGGTAGCCGCGCGCTGGAGTCGCGCGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23403910..23404150 26863196 MeRIP-seq:(Medium) rs1389597512 Functional Loss SNV dbSNP153 33..33 33 - - - 99360 RMVar_ID_99360 Human_SNP_ID_356027646 m1A Human chr8 - 23457608 23457608 23457608 GAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGATGCTGCCCACTGGTGGTCCCCCGCTCCCGGGG GAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGGTGCTGCCCACTGGTGGTCCCCCGCTCCCGGGG T C ENTPD4 Ensembl:ENSG00000197217 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:23457549..23457644;chr8:23457498..23457611;chr8:23457327..23457646 26863196 MeRIP-seq:(Medium) rs1038758299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796192,Human_RBP_ID_4994951,Human_RBP_ID_5480925,Human_RBP_ID_18426807 Human_Splice_Rec_958567,Human_Splice_Rec_958599,Human_Splice_Rec_958625,Human_Splice_Rec_958649,Human_Splice_Rec_958683 RMVar_hsa_circ_90388,RMVar_hsa_circ_250794 99361 RMVar_ID_99361 Human_SNP_ID_356027647 m1A Human chr8 - 23457608 23457608 23457608 GAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGATGCTGCCCACTGGTGGTCCCCCGCTCCCGGGG GAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGCTGCTGCCCACTGGTGGTCCCCCGCTCCCGGGG T G ENTPD4 Ensembl:ENSG00000197217 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:23457549..23457644;chr8:23457498..23457611;chr8:23457327..23457646 26863196 MeRIP-seq:(Medium) rs1038758299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796192,Human_RBP_ID_4994951,Human_RBP_ID_5480925,Human_RBP_ID_18426807 Human_Splice_Rec_958567,Human_Splice_Rec_958599,Human_Splice_Rec_958625,Human_Splice_Rec_958649,Human_Splice_Rec_958683 RMVar_hsa_circ_90388,RMVar_hsa_circ_250794 99362 RMVar_ID_99362 Human_SNP_ID_356027665 m1A Human chr8 - 23457627 23457627 23457627 GGGTGCGGCTCCAGGAAAGGAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGATGCTGCCCACTGG GGGTGCGGCTCCAGGAAAGGAGCGCGGCCTCCGGGAAGCCGGCTGGCCGTGATGCTGCCCACTGG T C ENTPD4 Ensembl:ENSG00000197217 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23457407..23457661 26863196 MeRIP-seq:(Medium) rs1014054890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796192,Human_RBP_ID_4995979,Human_RBP_ID_18426807 Human_Splice_Rec_958567,Human_Splice_Rec_958599,Human_Splice_Rec_958625,Human_Splice_Rec_958649,Human_Splice_Rec_958683 RMVar_hsa_circ_90388,RMVar_hsa_circ_250794 99363 RMVar_ID_99363 Human_SNP_ID_356027666 m1A Human chr8 - 23457627 23457627 23457627 GGGTGCGGCTCCAGGAAAGGAGCGCGGCCTCCAGGAAGCCGGCTGGCCGTGATGCTGCCCACTGG GGGTGCGGCTCCAGGAAAGGAGCGCGGCCTCCCGGAAGCCGGCTGGCCGTGATGCTGCCCACTGG T G ENTPD4 Ensembl:ENSG00000197217 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23457407..23457661 26863196 MeRIP-seq:(Medium) rs1014054890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796192,Human_RBP_ID_4995979,Human_RBP_ID_18426807 Human_Splice_Rec_958567,Human_Splice_Rec_958599,Human_Splice_Rec_958625,Human_Splice_Rec_958649,Human_Splice_Rec_958683 RMVar_hsa_circ_90388,RMVar_hsa_circ_250794 99364 RMVar_ID_99364 Human_SNP_ID_356045465 m1A Human chr8 + 23529063 23529063 23529063 GCCAGGCGGTGGCGCGGAGGATGGATGGGGACAGCCGAGATGGCGGCGGCGGCAAGGACGCCACC GCCAGGCGGTGGCGCGGAGGATGGATGGGGACTGCCGAGATGGCGGCGGCGGCAAGGACGCCACC A T SLC25A37 Ensembl:ENSG00000147454 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23528907..23529161 26863196 MeRIP-seq:(Medium) rs1050865824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796315,Human_RBP_ID_4979911,Human_RBP_ID_5328804,Human_RBP_ID_9263987,Human_RBP_ID_9313325,Human_RBP_ID_23087841,Human_RBP_ID_26772432 99365 RMVar_ID_99365 Human_SNP_ID_356049677 m1A Human chr8 + 23544933 23544933 23544933 GCCTCCTCCCAGGTGGGAACTTTCACTGTCGAACTAAGGACCCGAGGAGGGTGGAAACAGGAGGA GCCTCCTCCCAGGTGGGAACTTTCACTGTCGATCTAAGGACCCGAGGAGGGTGGAAACAGGAGGA A T SLC25A37 Ensembl:ENSG00000147454 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:23544928..23545008 26863196 MeRIP-seq:(Medium) rs1172370373 Functional Loss SNV dbSNP153 33..33 33 - - - 99366 RMVar_ID_99366 Human_SNP_ID_356056929 m1A Human chr8 - 23571602 23571602 23571602 CCTGAGTGTTCAGAAGGGTCTTACAGACGTCCAGGGGGGTCGTGGCGGCCGCGGCGAGGGCCCCG CCTGAGTGTTCAGAAGGGTCTTACAGACGTCCGGGGGGGTCGTGGCGGCCGCGGCGAGGGCCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23571533..23571604 26863196 MeRIP-seq:(Medium) rs774935400 Functional Loss SNV dbSNP153 33..33 33 - - - 99367 RMVar_ID_99367 Human_SNP_ID_356084501 m1A Human chr8 + 23679780 23679780 23679780 CAGGGCCTAGGCTGCCTTCTTTTCCATGTCCCACCCATGAGCCCTCCACTGGACAGCTCAGTAAG CAGGGCCTAGGCTGCCTTCTTTTCCATGTCCCGCCCATGAGCCCTCCACTGGACAGCTCAGTAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23679731..23679814 26863196 MeRIP-seq:(Medium) rs183120348 Functional Loss SNV dbSNP153 33..33 33 - - - 99368 RMVar_ID_99368 Human_SNP_ID_356226467 m1A Human chr8 + 24235890 24235890 24235890 TGGAGACATGAGTCTGCTGATGCTCCCAGCTGAATAAAGCCCTTCCTTCTACAACTCAGTGTCTG TGGAGACATGAGTCTGCTGATGCTCCCAGCTGCATAAAGCCCTTCCTTCTACAACTCAGTGTCTG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:24235812..24235899 26863410 MeRIP-seq:(Medium) rs190188560 Functional Loss SNV dbSNP153 33..33 33 - - - 99369 RMVar_ID_99369 Human_SNP_ID_356412574 m1A Human chr8 - 24953502 24953502 24953502 GGAGGAGGAGAAGGACAAGGAAGAGGCCGAGGAAGAGGAGGCAGCTGAAGAGGAAGAAGGTATGA GGAGGAGGAGAAGGACAAGGAAGAGGCCGAGGGAGAGGAGGCAGCTGAAGAGGAAGAAGGTATGA T C NEFL Ensembl:ENSG00000277586 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:24952826..24953567 26863196 MeRIP-seq:(Medium) rs770391341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_959243,Human_Splice_Rec_959249,Human_Splice_Rec_959255 RMVar_hsa_circ_21424 99370 RMVar_ID_99370 Human_SNP_ID_356493515 m1A Human chr8 - 25263665 25263665 25263665 CTAAGTGGGGCGAGGGGGTATCCGCACATAGGACTTGGGGGTGGTGCACTGGCCTCGGATAGCTG CTAAGTGGGGCGAGGGGGTATCCGCACATAGGGCTTGGGGGTGGTGCACTGGCCTCGGATAGCTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:25263600..25263713 26863196 MeRIP-seq:(Medium) rs1313745140 Functional Loss SNV dbSNP153 33..33 33 - - - 99371 RMVar_ID_99371 Human_SNP_ID_356500228 m1A Human chr8 - 25290927 25290927 25290927 CCCCACCCCTATCCTTTTCTGACTCACACTACACCCTCTGCCAACTGGTAATTCTGATTTCTTCA CCCCACCCCTATCCTTTTCTGACTCACACTACGCCCTCTGCCAACTGGTAATTCTGATTTCTTCA T C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:25290925..25291059 26863196 MeRIP-seq:(Medium) rs1041819181 Functional Loss SNV dbSNP153 33..33 33 - - - 99372 RMVar_ID_99372 Human_SNP_ID_356508689 m1A Human chr8 - 25323457 25323457 25323457 ACCTCTTCTCTTTATTTCTACAAGACCTTCCCAGCGCATCTCTCTGTCTCTAGGCTCTCCCACCA ACCTCTTCTCTTTATTTCTACAAGACCTTCCCGGCGCATCTCTCTGTCTCTAGGCTCTCCCACCA T C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:25323453..25323613 26863196 MeRIP-seq:(Medium) rs907496259 Functional Loss SNV dbSNP153 33..33 33 - - - 99373 RMVar_ID_99373 Human_SNP_ID_356524994 m1A Human chr8 + 25385422 25385422 25385422 AATACTAGAGGGGTGGAGATGAGGTCACAGCCATCTGATGATTGATGGGCTGTGTGGGTGAGGAA AATACTAGAGGGGTGGAGATGAGGTCACAGCCGTCTGATGATTGATGGGCTGTGTGGGTGAGGAA A G DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:25385372..25385535 26863196 MeRIP-seq:(Medium) rs887332389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35702,RMVar_hsa_circ_53719,RMVar_hsa_circ_62701,RMVar_hsa_circ_4994,RMVar_hsa_circ_97886,RMVar_hsa_circ_250848,RMVar_hsa_circ_78707,RMVar_hsa_circ_250852,RMVar_hsa_circ_118568,RMVar_hsa_circ_265906,RMVar_hsa_circ_250857,RMVar_hsa_circ_69271,RMVar_hsa_circ_76100,RMVar_hsa_circ_352088,RMVar_hsa_circ_364921,RMVar_hsa_circ_250859,RMVar_hsa_circ_370880,RMVar_hsa_circ_357611,RMVar_hsa_circ_350174,RMVar_hsa_circ_314861,RMVar_hsa_circ_250862,RMVar_hsa_circ_250863,RMVar_hsa_circ_250861,RMVar_hsa_circ_67615,RMVar_hsa_circ_32052,RMVar_hsa_circ_7059,RMVar_hsa_circ_354016,RMVar_hsa_circ_38745,RMVar_hsa_circ_34842,RMVar_hsa_circ_354317,RMVar_hsa_circ_2132,RMVar_hsa_circ_14084 99374 RMVar_ID_99374 Human_SNP_ID_356525191 m1A Human chr8 + 25386255 25386255 25386255 CTTGTATGGAGTTAAAATAACCGTGGTTGGGGATGAGGTGGACCAGGCAGAGGAAAGAATAAAGA CTTGTATGGAGTTAAAATAACCGTGGTTGGGGGTGAGGTGGACCAGGCAGAGGAAAGAATAAAGA A G DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:25386206..25386341 26863196 MeRIP-seq:(Medium) rs949672342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35702,RMVar_hsa_circ_53719,RMVar_hsa_circ_62701,RMVar_hsa_circ_4994,RMVar_hsa_circ_97886,RMVar_hsa_circ_250848,RMVar_hsa_circ_78707,RMVar_hsa_circ_250852,RMVar_hsa_circ_118568,RMVar_hsa_circ_265906,RMVar_hsa_circ_250857,RMVar_hsa_circ_69271,RMVar_hsa_circ_76100,RMVar_hsa_circ_352088,RMVar_hsa_circ_364921,RMVar_hsa_circ_250859,RMVar_hsa_circ_370880,RMVar_hsa_circ_357611,RMVar_hsa_circ_350174,RMVar_hsa_circ_314861,RMVar_hsa_circ_250862,RMVar_hsa_circ_250863,RMVar_hsa_circ_250861,RMVar_hsa_circ_67615,RMVar_hsa_circ_32052,RMVar_hsa_circ_7059,RMVar_hsa_circ_354016,RMVar_hsa_circ_38745,RMVar_hsa_circ_34842,RMVar_hsa_circ_354317,RMVar_hsa_circ_2132,RMVar_hsa_circ_14084 99375 RMVar_ID_99375 Human_SNP_ID_356531502 m1A Human chr8 + 25410106 25410106 25410106 CGCCTGCACTTTCTGTCATTTCTAGGCTCCCCATCGTTGCAGACAGATGGAATCGCGGCCACTCC CGCCTGCACTTTCTGTCATTTCTAGGCTCCCCGTCGTTGCAGACAGATGGAATCGCGGCCACTCC A G DOCK5 Ensembl:ENSG00000147459 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:25410101..25410209 26863196 MeRIP-seq:(Medium) rs2709618 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19140965 Human_Splice_Rec_959370,Human_Splice_Rec_959371,Human_Splice_Rec_959528,Human_Splice_Rec_959529,Human_Splice_Rec_959541,Human_Splice_Rec_959543 GWAS_ID_13112,GWAS_ID_13113,GWAS_ID_13114 RMVar_hsa_circ_265906,RMVar_hsa_circ_26083,RMVar_hsa_circ_250869,RMVar_hsa_circ_344705 99376 RMVar_ID_99376 Human_SNP_ID_356531554 m1A Human chr8 - 25410199 25410199 25410199 GCCACAGTTGCCAGCTGTGATTTCCCTACCTCAGTGGAGTTCCTCTGGCTGCCTTCATAGGGCTT GCCACAGTTGCCAGCTGTGATTTCCCTACCTCGGTGGAGTTCCTCTGGCTGCCTTCATAGGGCTT T C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:25410176..25410225 26863196 MeRIP-seq:(Medium) rs1310284339 Functional Loss SNV dbSNP153 33..33 33 - - - 99377 RMVar_ID_99377 Human_SNP_ID_356532019 m1A Human chr8 + 25411160 25411160 25411160 GAGGAGAAGGCAGAATTGGGAAGAAAGCTAAGACCTGCTTCTAATTTTGTGTTTCTGCTTCTGCA GAGGAGAAGGCAGAATTGGGAAGAAAGCTAAGCCCTGCTTCTAATTTTGTGTTTCTGCTTCTGCA A C DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:25411159..25411276 26863196 MeRIP-seq:(Medium) rs746679786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265906 99378 RMVar_ID_99378 Human_SNP_ID_356532020 m1A Human chr8 + 25411160 25411160 25411160 GAGGAGAAGGCAGAATTGGGAAGAAAGCTAAGACCTGCTTCTAATTTTGTGTTTCTGCTTCTGCA GAGGAGAAGGCAGAATTGGGAAGAAAGCTAAGGCCTGCTTCTAATTTTGTGTTTCTGCTTCTGCA A G DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:25411159..25411276 26863196 MeRIP-seq:(Medium) rs746679786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265906 99379 RMVar_ID_99379 Human_SNP_ID_356541450 m1A Human chr8 - 25450426 25450426 25450426 ACTGTCACACAAAAAAGGTGTGTCCTACTTCAACACTCAACATTCAAGAAATATTTGTCAAAGAC ACTGTCACACAAAAAAGGTGTGTCCTACTTCAGCACTCAACATTCAAGAAATATTTGTCAAAGAC T C KCTD9 Ensembl:ENSG00000104756 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:25450421..25450530;chr8:25450421..25450551 26863196 MeRIP-seq:(Medium) rs1325530608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18116175 Human_Splice_Rec_959628,Human_Splice_Rec_959629,Human_Splice_Rec_959658,Human_Splice_Rec_959659,Human_Splice_Rec_959665,Human_Splice_Rec_959668 RMVar_hsa_circ_69276,RMVar_hsa_circ_326968 99380 RMVar_ID_99380 Human_SNP_ID_356543503 m1A Human chr8 + 25458274 25458274 25458274 CTCATCGCGCTGCCCCCGCTGGGTCCTGAGTGAGCCGCCACCCTCCCACCTGGTCCTCCTCCCAC CTCATCGCGCTGCCCCCGCTGGGTCCTGAGTGTGCCGCCACCCTCCCACCTGGTCCTCCTCCCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:25457732..25458469 26863196 MeRIP-seq:(Medium) rs1217568240 Functional Loss SNV dbSNP153 33..33 33 - - - 99381 RMVar_ID_99381 Human_SNP_ID_356543932 m1A Human chr8 + 25459262 25459262 25459262 GGTGGAGGAGGCTGCCGGGCAGAGCGCAGGCCAGGATCAGCGCAGGCTGTGAGTCCAGGTCAGCC GGTGGAGGAGGCTGCCGGGCAGAGCGCAGGCCGGGATCAGCGCAGGCTGTGAGTCCAGGTCAGCC A G CDCA2 Ensembl:ENSG00000184661 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:25459128..25459338 26863196 MeRIP-seq:(Medium) rs1012016064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957649,Human_RBP_ID_4995384,Human_RBP_ID_9441401,Human_RBP_ID_18427093,Human_RBP_ID_19021892,Human_RBP_ID_22426701,Human_RBP_ID_22747512,Human_RBP_ID_23088084,Human_RBP_ID_26358894,Human_RBP_ID_26772436 99382 RMVar_ID_99382 Human_SNP_ID_356544257 m1A Human chr8 - 25460321 25460321 25460321 GACAACTCTCTGTCTAAACCTTCAACTTCACAAGGAGGCAGATCATCACATACCAGCATTATTCA GACAACTCTCTGTCTAAACCTTCAACTTCACAGGGAGGCAGATCATCACATACCAGCATTATTCA T C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:25460320..25460417 26863196 MeRIP-seq:(Medium) rs1365115888 Functional Loss SNV dbSNP153 33..33 33 - - - 99383 RMVar_ID_99383 Human_SNP_ID_356557162 m1A Human chr8 + 25507295 25507295 25507295 ATTCTGAACTGTTTAAAGATTTGTCTGATGCCATTGAGCAAACCTTTCAGAGGAGAAATAGTGAA ATTCTGAACTGTTTAAAGATTTGTCTGATGCCGTTGAGCAAACCTTTCAGAGGAGAAATAGTGAA A G CDCA2 Ensembl:ENSG00000184661 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79983029 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8685211,Human_RBP_ID_9223304,Human_RBP_ID_24253776 Human_miRNA_ID_1409773 99384 RMVar_ID_99384 Human_SNP_ID_356686311 m1A Human chr8 + 26002912 26002908 26002912 GGGCAGGCGGGCAGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG GGGCAGGCGGGCAGGCAGGCGGGCAGGCG____GGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG GGGCA G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26002879..26002944 26863196 MeRIP-seq:(Medium) rs1563204739 Functional Loss DEL dbSNP153 30..33 33 - - - 99385 RMVar_ID_99385 Human_SNP_ID_356686316 m1A Human chr8 + 26002912 26002911 26002912 GGGCAGGCGGGCAGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG GGGCAGGCGGGCAGGCAGGCGGGCAGGCGGGC_GGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG CA C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26002879..26002944 26863196 MeRIP-seq:(Medium) rs1417713344 Functional Loss DEL dbSNP153 33..33 33 - - - 99386 RMVar_ID_99386 Human_SNP_ID_356686318 m1A Human chr8 + 26002912 26002912 26002912 GGGCAGGCGGGCAGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG GGGCAGGCGGGCAGGCAGGCGGGCAGGCGGGCGGGCGGGCAGGCGGGCAGGCAGGCAGGCAGGCG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26002879..26002944 26863196 MeRIP-seq:(Medium) rs1173319065 Functional Loss SNV dbSNP153 33..33 33 - - - 99387 RMVar_ID_99387 Human_SNP_ID_356762836 m1A Human chr8 - 26291581 26291551 26291581 CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCGACTACGACAGCGACGGCGGCGGCGGCAGCGGCA CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCG______________________________GCA CCGCTGCCGCCGCCGCCGTCGCTGTCGTAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:26291540..26291663;chr8:26291531..26291662;chr8:26291536..26291661 26863196 MeRIP-seq:(Medium) rs1232786012 Functional Loss DEL dbSNP153 33..62 33 - - - 99388 RMVar_ID_99388 Human_SNP_ID_356762845 m1A Human chr8 - 26291581 26291555 26291582 CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCGACTACGACAGCGACGGCGGCGGCGGCAGCGGCA CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGC___________________________AGCGGCA TGCCGCCGCCGCCGTCGCTGTCGTAGTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:26291540..26291663;chr8:26291531..26291662;chr8:26291536..26291661 26863196 MeRIP-seq:(Medium) rs1272725065 Functional Loss DEL dbSNP153 32..58 33 - - - 99389 RMVar_ID_99389 Human_SNP_ID_356762852 m1A Human chr8 - 26291581 26291557 26291581 CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCGACTACGACAGCGACGGCGGCGGCGGCAGCGGCA CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCG________________________GCAGCGGCA CCGCCGCCGCCGTCGCTGTCGTAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:26291540..26291663;chr8:26291531..26291662;chr8:26291536..26291661 26863196 MeRIP-seq:(Medium) rs1175290421 Functional Loss DEL dbSNP153 33..56 33 - - - 99390 RMVar_ID_99390 Human_SNP_ID_356762874 m1A Human chr8 - 26291581 26291581 26291581 CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCGACTACGACAGCGACGGCGGCGGCGGCAGCGGCA CTCGTGCTCTTTCTCCGGCAGCGGCGGCGGCGGCTACGACAGCGACGGCGGCGGCGGCAGCGGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:26291540..26291663;chr8:26291531..26291662;chr8:26291536..26291661 26863196 MeRIP-seq:(Medium) rs1156586793 Functional Loss SNV dbSNP153 33..33 33 - - - 99391 RMVar_ID_99391 Human_SNP_ID_356768645 m1A Human chr8 + 26313658 26313658 26313658 ATCATCCTAGGTTATCCTGGTAGGCTGTAAATATGTAAGCACAAGGATGCTATAAAAGGGAGGCA ATCATCCTAGGTTATCCTGGTAGGCTGTAAATGTGTAAGCACAAGGATGCTATAAAAGGGAGGCA A G PPP2R2A Ensembl:ENSG00000221914 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26313655..26313775 26863196 MeRIP-seq:(Medium) rs59183476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7826393,Human_RBP_ID_9223382,Human_RBP_ID_16396932 RMVar_hsa_circ_59757 99392 RMVar_ID_99392 Human_SNP_ID_356786440 m1A Human chr8 + 26383130 26383130 26383130 TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACAATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACGATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC A G BNIP3L Ensembl:ENSG00000104765 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26383079..26383327 26863196 MeRIP-seq:(Medium) rs1055479 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_960751,Human_RBP_ID_4994953 GWAS_ID_13115,GWAS_ID_13116,GWAS_ID_13117,GWAS_ID_13118 RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99393 RMVar_ID_99393 Human_SNP_ID_356786441 m1A Human chr8 + 26383130 26383130 26383130 TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACAATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACTATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC A T BNIP3L Ensembl:ENSG00000104765 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26383079..26383327 26863196 MeRIP-seq:(Medium) rs1055479 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_960751,Human_RBP_ID_4994953 GWAS_ID_13115,GWAS_ID_13116,GWAS_ID_13117,GWAS_ID_13118 RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99394 RMVar_ID_99394 Human_SNP_ID_356786447 m1A Human chr8 - 26383144 26383144 26383144 TGTTGTTGTGCAGGGGCGGCGGCGGCTCGACTAGGTGGGACGACATTGTCGGACAGCTGGCAGGA TGTTGTTGTGCAGGGGCGGCGGCGGCTCGACTGGGTGGGACGACATTGTCGGACAGCTGGCAGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:26383095..26383221 26863196 MeRIP-seq:(Medium) rs1397123860 Functional Loss SNV dbSNP153 33..33 33 - - - 99395 RMVar_ID_99395 Human_SNP_ID_356786463 m1A Human chr8 + 26383168 26383168 26383168 GTCCCACCTAGTCGAGCCGCCGCCGCCCCTGCACAACAACAACAACAACTGCGAGGAAAATGAGC GTCCCACCTAGTCGAGCCGCCGCCGCCCCTGCGCAACAACAACAACAACTGCGAGGAAAATGAGC A G BNIP3L Ensembl:ENSG00000104765 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:26383076..26383195 26863410 MeRIP-seq:(Medium) rs1459453584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960751,Human_RBP_ID_4995387 Human_Splice_Rec_960183,Human_Splice_Rec_960189,Human_Splice_Rec_960199 RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99396 RMVar_ID_99396 Human_SNP_ID_356786494 m1A Human chr8 + 26383228 26383228 26383228 TGAGCAGTCTCTGCCCCCGCCGGCCGGCCTCAACAGTGAGTGCGGGGCCGAGGCTCTGTGAAGGG TGAGCAGTCTCTGCCCCCGCCGGCCGGCCTCATCAGTGAGTGCGGGGCCGAGGCTCTGTGAAGGG A T BNIP3L Ensembl:ENSG00000104765 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:26383144..26383391 32194978 MeRIP-seq:(Medium) rs1228713235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3973002,Human_RBP_ID_4996529,Human_RBP_ID_5224649,Human_RBP_ID_9405283,Human_RBP_ID_19140977,Human_RBP_ID_22465484,Human_RBP_ID_26359692,Human_RBP_ID_26832624 Human_Splice_Rec_960183,Human_Splice_Rec_960189,Human_Splice_Rec_960199 RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99397 RMVar_ID_99397 Human_SNP_ID_356788581 m1A Human chr8 + 26391193 26391193 26391193 TCTGGATTCACCATGTTCACATCTGTGTGCACATGACAGATTTCAGTTCTGCTGTGGTTAACTTA TCTGGATTCACCATGTTCACATCTGTGTGCACCTGACAGATTTCAGTTCTGCTGTGGTTAACTTA A C BNIP3L Ensembl:ENSG00000104765 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:26391191..26391273 26863196 MeRIP-seq:(Medium) rs751582559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99398 RMVar_ID_99398 Human_SNP_ID_356788582 m1A Human chr8 + 26391193 26391193 26391193 TCTGGATTCACCATGTTCACATCTGTGTGCACATGACAGATTTCAGTTCTGCTGTGGTTAACTTA TCTGGATTCACCATGTTCACATCTGTGTGCACGTGACAGATTTCAGTTCTGCTGTGGTTAACTTA A G BNIP3L Ensembl:ENSG00000104765 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:26391191..26391273 26863196 MeRIP-seq:(Medium) rs751582559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 99399 RMVar_ID_99399 Human_SNP_ID_356819813 m1A Human chr8 + 26514309 26514309 26514309 TGGCAGACGGACGGACGGACGGCGAGGACCCTACCCGAGCCCCCGAGCCATGGCCGAGAGAAAGC TGGCAGACGGACGGACGGACGGCGAGGACCCTCCCCGAGCCCCCGAGCCATGGCCGAGAGAAAGC A C DPYSL2 Ensembl:ENSG00000092964 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:26514153..26514355 26863196 MeRIP-seq:(Medium) rs978562293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103604,RMVar_hsa_circ_250902 99400 RMVar_ID_99400 Human_SNP_ID_356836092 m1A Human chr8 - 26577204 26577204 26577204 CGGGGAATGGGCGCGGGCCGGGGGGAGGCTGCAGAGACGGGATCTGGCCCGCGTGGAGGCGCCGG CGGGGAATGGGCGCGGGCCGGGGGGAGGCTGCGGAGACGGGATCTGGCCCGCGTGGAGGCGCCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:26577154..26577238 26863196 MeRIP-seq:(Medium) rs1200537773 Functional Loss SNV dbSNP153 33..33 33 - - - 99401 RMVar_ID_99401 Human_SNP_ID_356836166 m1A Human chr8 - 26577307 26577307 26577307 CTGGAACGGCGGCGGGCGGGAACCCGGCGGGGAGGGCCCGGCCACGCCCGGCCCCGGAGAGGGCG CTGGAACGGCGGCGGGCGGGAACCCGGCGGGGGGGGCCCGGCCACGCCCGGCCCCGGAGAGGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26577275..26577390 26863196 MeRIP-seq:(Medium) rs937327616 Functional Loss SNV dbSNP153 33..33 33 - - - 99402 RMVar_ID_99402 Human_SNP_ID_357069565 m1A Human chr8 + 27491199 27491199 27491199 GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGACCCGCCGCCATGACGCTGCGCGCGGCCGTCTT GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGCCCCGCCGCCATGACGCTGCGCGCGGCCGTCTT A C EPHX2 Ensembl:ENSG00000120915 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27491194..27491259 26863196 MeRIP-seq:(Medium) rs905914545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995389,Human_RBP_ID_9313351 Human_Splice_Rec_960968 99403 RMVar_ID_99403 Human_SNP_ID_357069566 m1A Human chr8 + 27491199 27491199 27491199 GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGACCCGCCGCCATGACGCTGCGCGCGGCCGTCTT GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGGCCCGCCGCCATGACGCTGCGCGCGGCCGTCTT A G EPHX2 Ensembl:ENSG00000120915 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27491194..27491259 26863196 MeRIP-seq:(Medium) rs905914545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995389,Human_RBP_ID_9313351 Human_Splice_Rec_960968 99404 RMVar_ID_99404 Human_SNP_ID_357097108 m1A Human chr8 + 27598113 27598113 27598113 TGCAGGATCCAGAGCGGGGAGAGGCTGGGCGGAGTTGGGGGCCTGGAGGCTGGGGCCTGGTTACT TGCAGGATCCAGAGCGGGGAGAGGCTGGGCGGTGTTGGGGGCCTGGAGGCTGGGGCCTGGTTACT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27597976..27598203 26863196 MeRIP-seq:(Medium) rs1475599664 Functional Loss SNV dbSNP153 33..33 33 - - - 99405 RMVar_ID_99405 Human_SNP_ID_357097122 m1A Human chr8 - 27598142 27598142 27598142 CCCCCCAGAGAGAGCTCTGCACGTCACCAAGTAACCAGGCCCCAGCCTCCAGGCCCCCAACTCCG CCCCCCAGAGAGAGCTCTGCACGTCACCAAGTGACCAGGCCCCAGCCTCCAGGCCCCCAACTCCG T C CLU Ensembl:ENSG00000120885 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr8:27597960..27598275;chr8:27598037..27598238;chr8:27598001..27598202 26863196 MeRIP-seq:(Medium) rs765918806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795553,Human_RBP_ID_845893,Human_RBP_ID_5123459,Human_RBP_ID_17665939,Human_RBP_ID_22465156,Human_RBP_ID_27537753 Human_miRNA_ID_1208191,Human_miRNA_ID_2684154,Human_miRNA_ID_2714081,Human_miRNA_ID_3050061 RMVar_hsa_circ_82519,RMVar_hsa_circ_250949 99406 RMVar_ID_99406 Human_SNP_ID_357097158 m1A Human chr8 - 27598203 27598203 27598203 GGATGTTGCTTTTGCACCTACGGGGGCATCTGAGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCC GGATGTTGCTTTTGCACCTACGGGGGCATCTGGGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCC T C CLU Ensembl:ENSG00000120885 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:27598060..27598210 32194978 MeRIP-seq:(Medium) rs1308669861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88337,Human_RBP_ID_795554,Human_RBP_ID_8685451,Human_RBP_ID_17665941,Human_RBP_ID_21565240,Human_RBP_ID_22465158,Human_RBP_ID_22776002,Human_RBP_ID_24440880,Human_RBP_ID_24520026,Human_RBP_ID_27537761 Human_Splice_Rec_961232,Human_Splice_Rec_961248,Human_Splice_Rec_961262,Human_Splice_Rec_961276,Human_Splice_Rec_961280 Human_miRNA_ID_131261,Human_miRNA_ID_132344,Human_miRNA_ID_1149363,Human_miRNA_ID_1152224,Human_miRNA_ID_1153519,Human_miRNA_ID_1156103,Human_miRNA_ID_1229518,Human_miRNA_ID_1509513,Human_miRNA_ID_2541727,Human_miRNA_ID_2543606,Human_miRNA_ID_2545456,Human_miRNA_ID_2547310,Human_miRNA_ID_2549175,Human_miRNA_ID_2551043,Human_miRNA_ID_2556448,Human_miRNA_ID_2558330,Human_miRNA_ID_2588747 RMVar_hsa_circ_82519,RMVar_hsa_circ_250949 99407 RMVar_ID_99407 Human_SNP_ID_357097233 m1A Human chr8 - 27598417 27598414 27598418 GGGCCTTTCCTGCGGGCCTGCAGGGCCCAGTGAGTCTCTGGGAGCCACAAAAAAACAAACAAAGT GGGCCTTTCCTGCGGGCCTGCAGGGCCCAGT____CTCTGGGAGCCACAAAAAAACAAACAAAGT GACTC G CLU Ensembl:ENSG00000120885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:27598415..27598671 26863196 MeRIP-seq:(Medium) rs1357992600 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_24254361 RMVar_hsa_circ_82519,RMVar_hsa_circ_250949 99408 RMVar_ID_99408 Human_SNP_ID_357097237 m1A Human chr8 - 27598417 27598417 27598417 GGGCCTTTCCTGCGGGCCTGCAGGGCCCAGTGAGTCTCTGGGAGCCACAAAAAAACAAACAAAGT GGGCCTTTCCTGCGGGCCTGCAGGGCCCAGTGCGTCTCTGGGAGCCACAAAAAAACAAACAAAGT T G CLU Ensembl:ENSG00000120885 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:27598415..27598671 26863196 MeRIP-seq:(Medium) rs1331064062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24254361 RMVar_hsa_circ_82519,RMVar_hsa_circ_250949 99409 RMVar_ID_99409 Human_SNP_ID_357099405 m1A Human chr8 + 27606462 27606462 27606462 TTACACTCTTCCCAGAGGGCCATCATGGTCTCATTGCACACTCCTGGGAGCTCCTTCAGCTTTGT TTACACTCTTCCCAGAGGGCCATCATGGTCTCGTTGCACACTCCTGGGAGCTCCTTCAGCTTTGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27606411..27606583 26863196 MeRIP-seq:(Medium) rs781182159 Functional Loss SNV dbSNP153 33..33 33 - - - 99410 RMVar_ID_99410 Human_SNP_ID_357100028 m1A Human chr8 - 27609062 27609062 27609062 TCTTGCAGAAATGTCCAATCAGGGAAGTAAGTACGTCAATAAGGAAATTCAAAATGCTGTCAACG TCTTGCAGAAATGTCCAATCAGGGAAGTAAGTGCGTCAATAAGGAAATTCAAAATGCTGTCAACG T C CLU Ensembl:ENSG00000120885 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:27608963..27609064 32194978 MeRIP-seq:(Medium) rs1390112562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89751,Human_RBP_ID_3154343,Human_RBP_ID_5000011,Human_RBP_ID_9223716,Human_RBP_ID_17672396,Human_RBP_ID_24549553 Human_Splice_Rec_961220,Human_Splice_Rec_961236,Human_Splice_Rec_961250,Human_Splice_Rec_961266,Human_Splice_Rec_961292,Human_Splice_Rec_961304,Human_Splice_Rec_961314,Human_Splice_Rec_961322,Human_Splice_Rec_961328,Human_Splice_Rec_961336,Human_Splice_Rec_961342,Human_Splice_Rec_961346,Human_Splice_Rec_961352 RMVar_hsa_circ_65688,RMVar_hsa_circ_65978,RMVar_hsa_circ_352255 99411 RMVar_ID_99411 Human_SNP_ID_357100031 m1A Human chr8 - 27609077 27609077 27609077 TGCCTCTTGCACTTCTCTTGCAGAAATGTCCAATCAGGGAAGTAAGTACGTCAATAAGGAAATTC TGCCTCTTGCACTTCTCTTGCAGAAATGTCCAGTCAGGGAAGTAAGTACGTCAATAAGGAAATTC T C CLU Ensembl:ENSG00000120885 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:27609026..27609100 26863196 MeRIP-seq:(Medium) rs1453425479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89751,Human_RBP_ID_9406158,Human_RBP_ID_17672396 Human_Splice_Rec_961220,Human_Splice_Rec_961236,Human_Splice_Rec_961250,Human_Splice_Rec_961266,Human_Splice_Rec_961292,Human_Splice_Rec_961304,Human_Splice_Rec_961314,Human_Splice_Rec_961322,Human_Splice_Rec_961328,Human_Splice_Rec_961336,Human_Splice_Rec_961342,Human_Splice_Rec_961346,Human_Splice_Rec_961352 RMVar_hsa_circ_65688,RMVar_hsa_circ_65978,RMVar_hsa_circ_352255 99412 RMVar_ID_99412 Human_SNP_ID_357100032 m1A Human chr8 - 27609078 27609078 27609078 CTGCCTCTTGCACTTCTCTTGCAGAAATGTCCAATCAGGGAAGTAAGTACGTCAATAAGGAAATT CTGCCTCTTGCACTTCTCTTGCAGAAATGTCCGATCAGGGAAGTAAGTACGTCAATAAGGAAATT T C CLU Ensembl:ENSG00000120885 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:27608926..27609186 26863196 MeRIP-seq:(Medium) rs201809865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89751,Human_RBP_ID_9406158,Human_RBP_ID_17672396 Human_Splice_Rec_961220,Human_Splice_Rec_961236,Human_Splice_Rec_961250,Human_Splice_Rec_961266,Human_Splice_Rec_961292,Human_Splice_Rec_961304,Human_Splice_Rec_961314,Human_Splice_Rec_961322,Human_Splice_Rec_961328,Human_Splice_Rec_961336,Human_Splice_Rec_961342,Human_Splice_Rec_961346,Human_Splice_Rec_961352 RMVar_hsa_circ_65688,RMVar_hsa_circ_65978,RMVar_hsa_circ_352255 99413 RMVar_ID_99413 Human_SNP_ID_357100396 m1A Human chr8 + 27610529 27610529 27610529 CGTCTGGTCCCCCAGGACCTGCCCACTCTCCCAGGTCAGCAGCAGCCCCACAAACAGCAGCAGAG CGTCTGGTCCCCCAGGACCTGCCCACTCTCCCGGGTCAGCAGCAGCCCCACAAACAGCAGCAGAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:27610403..27610657 26863196 MeRIP-seq:(Medium) rs180798973 Functional Loss SNV dbSNP153 33..33 33 - - - 99414 RMVar_ID_99414 Human_SNP_ID_357100415 m1A Human chr8 - 27610592 27610592 27610592 ATGATGGTCTCCTGTTCTCTGCAGAGGCGTGCAAAGACTCCAGAATTGGAGGCATGATGAAGACT ATGATGGTCTCCTGTTCTCTGCAGAGGCGTGCGAAGACTCCAGAATTGGAGGCATGATGAAGACT T C CLU Ensembl:ENSG00000120885 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr8:27610413..27610625;chr8:27610392..27610625 26863196 MeRIP-seq:(Medium) rs765763029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796765,Human_RBP_ID_4994955,Human_RBP_ID_9405304,Human_RBP_ID_26358710 Human_Splice_Rec_961218,Human_Splice_Rec_961234,Human_Splice_Rec_961264,Human_Splice_Rec_961290,Human_Splice_Rec_961302,Human_Splice_Rec_961312,Human_Splice_Rec_961320,Human_Splice_Rec_961326,Human_Splice_Rec_961334,Human_Splice_Rec_961340,Human_Splice_Rec_961344,Human_Splice_Rec_961350,Human_Splice_Rec_961354 RMVar_hsa_circ_65978,RMVar_hsa_circ_352255,RMVar_hsa_circ_70688 99415 RMVar_ID_99415 Human_SNP_ID_357101538 m1A Human chr8 + 27614653 27614653 27614653 CTGCTCAAGGGTAGGGAAGACGGGGACATCTCACCGGTCAGCGGCACCCTGTGCCCGCGCGCTCC CTGCTCAAGGGTAGGGAAGACGGGGACATCTCCCCGGTCAGCGGCACCCTGTGCCCGCGCGCTCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:27614651..27614700 26863196 MeRIP-seq:(Medium) rs113754927 Functional Loss SNV dbSNP153 33..33 33 - - - 99416 RMVar_ID_99416 Human_SNP_ID_357106181 m1A Human chr8 + 27633902 27633902 27633902 GAGGAAGGGTGCGCGGGGCGAGGGGCGGCGGCAGACCTCGCGGGGCCCCAGCGGGAAGCGCGGGC GAGGAAGGGTGCGCGGGGCGAGGGGCGGCGGCTGACCTCGCGGGGCCCCAGCGGGAAGCGCGGGC A T SCARA3 Ensembl:ENSG00000168077 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:27633851..27634025 26863196 MeRIP-seq:(Medium) rs1472668405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995997 99417 RMVar_ID_99417 Human_SNP_ID_357106207 m1A Human chr8 + 27633975 27633975 27633975 GATGCGCGCTCTGGGCGGCGGGGCGCGGCGCTAGGCGCCCGGCGGGGCTTCCCCAGGCTGCGACC GATGCGCGCTCTGGGCGGCGGGGCGCGGCGCTGGGCGCCCGGCGGGGCTTCCCCAGGCTGCGACC A G SCARA3 Ensembl:ENSG00000168077 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:27633884..27634134 26863196 MeRIP-seq:(Medium) rs573063017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994957 99418 RMVar_ID_99418 Human_SNP_ID_357112686 m1A Human chr8 - 27658587 27658587 27658587 AGCTGCACCTCCTGGGCCAGAAGCAGCTTCTGAATTCCCTCCAGCTCCTCCTGCAGTTTTCGGAT AGCTGCACCTCCTGGGCCAGAAGCAGCTTCTGTATTCCCTCCAGCTCCTCCTGCAGTTTTCGGAT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:27658546..27658623 26863196 MeRIP-seq:(Medium) rs1284837988 Functional Loss SNV dbSNP153 33..33 33 - - - 99419 RMVar_ID_99419 Human_SNP_ID_357112936 m1A Human chr8 - 27659207 27659207 27659207 TTTCAATCTCGTGAGAAGCCATGCGTCCTTCCAGAGACTCAAACCTCTCCACAGTGCGGTTCTGG TTTCAATCTCGTGAGAAGCCATGCGTCCTTCCGGAGACTCAAACCTCTCCACAGTGCGGTTCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:27659166..27659384 26863196 MeRIP-seq:(Medium) rs1277688237 Functional Loss SNV dbSNP153 33..33 33 - - - 99420 RMVar_ID_99420 Human_SNP_ID_357115526 m1A Human chr8 - 27669109 27669109 27669109 GTCCCGACTCCTCCTGGGCTCACTTCTCCCCCAGGGCTTGTCCCCAGCTCCCTGGTACTCCACTC GTCCCGACTCCTCCTGGGCTCACTTCTCCCCCGGGGCTTGTCCCCAGCTCCCTGGTACTCCACTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:27669106..27669245 26863196 MeRIP-seq:(Medium) rs899104509 Functional Loss SNV dbSNP153 33..33 33 - - - 99421 RMVar_ID_99421 Human_SNP_ID_357115546 m1A Human chr8 + 27669163 27669163 27669163 GGAGTCGGGACAGAAGGAGGAGGCGAATGCCCACCCAGACAGGGAGGAGGGAGTGGCAGGAGAAG GGAGTCGGGACAGAAGGAGGAGGCGAATGCCCCCCCAGACAGGGAGGAGGGAGTGGCAGGAGAAG A C SCARA3 Ensembl:ENSG00000168077 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27668904..27669280 26863196 MeRIP-seq:(Medium) rs1342087665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250954,RMVar_hsa_circ_96679,RMVar_hsa_circ_118542,RMVar_hsa_circ_250953,RMVar_hsa_circ_104252,RMVar_hsa_circ_110394,RMVar_hsa_circ_250956,RMVar_hsa_circ_250958 99422 RMVar_ID_99422 Human_SNP_ID_357115547 m1A Human chr8 + 27669163 27669163 27669163 GGAGTCGGGACAGAAGGAGGAGGCGAATGCCCACCCAGACAGGGAGGAGGGAGTGGCAGGAGAAG GGAGTCGGGACAGAAGGAGGAGGCGAATGCCCTCCCAGACAGGGAGGAGGGAGTGGCAGGAGAAG A T SCARA3 Ensembl:ENSG00000168077 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27668904..27669280 26863196 MeRIP-seq:(Medium) rs1342087665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250954,RMVar_hsa_circ_96679,RMVar_hsa_circ_118542,RMVar_hsa_circ_250953,RMVar_hsa_circ_104252,RMVar_hsa_circ_110394,RMVar_hsa_circ_250956,RMVar_hsa_circ_250958 99423 RMVar_ID_99423 Human_SNP_ID_357140475 m1A Human chr8 - 27772530 27772530 27772530 TCACCGCACCGCTCCCGGGATCATGGTGTTCTACTTCACCAGCAGCAGCGGTGAGTGGGCGCCAC TCACCGCACCGCTCCCGGGATCATGGTGTTCTGCTTCACCAGCAGCAGCGGTGAGTGGGCGCCAC T C CCDC25 Ensembl:ENSG00000147419 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1289034493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995391,Human_RBP_ID_7827947,Human_RBP_ID_8238673,Human_RBP_ID_9338215,Human_RBP_ID_9405306,Human_RBP_ID_17714571,Human_RBP_ID_18426673 Human_Splice_Rec_961381,Human_Splice_Rec_961397,Human_Splice_Rec_961411,Human_Splice_Rec_961423,Human_Splice_Rec_961435,Human_Splice_Rec_961449,Human_Splice_Rec_961465,Human_Splice_Rec_961481 99424 RMVar_ID_99424 Human_SNP_ID_357140502 m1A Human chr8 + 27772574 27772574 27772574 ATCCCGGGAGCGGTGCGGTGACTCCACCGCGGAGCAGCAGCGCTCAACTCACGAAGCTCAGGATA ATCCCGGGAGCGGTGCGGTGACTCCACCGCGGGGCAGCAGCGCTCAACTCACGAAGCTCAGGATA A G ESCO2 Ensembl:ENSG00000171320 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:27772475..27772575 26863196 MeRIP-seq:(Medium) rs763141721 Functional Loss SNV dbSNP153 33..33 33 - - - 99425 RMVar_ID_99425 Human_SNP_ID_357140505 m1A Human chr8 + 27772580 27772580 27772580 GGAGCGGTGCGGTGACTCCACCGCGGAGCAGCAGCGCTCAACTCACGAAGCTCAGGATACCAGAC GGAGCGGTGCGGTGACTCCACCGCGGAGCAGCGGCGCTCAACTCACGAAGCTCAGGATACCAGAC A G ESCO2 Ensembl:ENSG00000171320 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27772494..27772580 26863196 MeRIP-seq:(Medium) rs1406376906 Functional Loss SNV dbSNP153 33..33 33 - - - 99426 RMVar_ID_99426 Human_SNP_ID_357141090 m1A Human chr8 + 27774600 27774600 27774600 TGGCTAGGCTGAGGAGAGCTCGCCGGGCTCTGAGGCGCAGGTAACCTCTGGAGTAGGCCGAGGCG TGGCTAGGCTGAGGAGAGCTCGCCGGGCTCTGGGGCGCAGGTAACCTCTGGAGTAGGCCGAGGCG A G ESCO2 Ensembl:ENSG00000171320 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:27774589..27774673 26863196 MeRIP-seq:(Medium) rs1008469334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995393 Human_Splice_Rec_961499,Human_Splice_Rec_961519 99427 RMVar_ID_99427 Human_SNP_ID_357141093 m1A Human chr8 + 27774606 27774606 27774606 GGCTGAGGAGAGCTCGCCGGGCTCTGAGGCGCAGGTAACCTCTGGAGTAGGCCGAGGCGGGGGGC GGCTGAGGAGAGCTCGCCGGGCTCTGAGGCGCCGGTAACCTCTGGAGTAGGCCGAGGCGGGGGGC A C ESCO2 Ensembl:ENSG00000171320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:27774577..27774657;chr8:27774597..27774685 26863196 MeRIP-seq:(Medium) rs1020168984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995393 Human_Splice_Rec_961499,Human_Splice_Rec_961519 99428 RMVar_ID_99428 Human_SNP_ID_357141094 m1A Human chr8 + 27774606 27774606 27774606 GGCTGAGGAGAGCTCGCCGGGCTCTGAGGCGCAGGTAACCTCTGGAGTAGGCCGAGGCGGGGGGC GGCTGAGGAGAGCTCGCCGGGCTCTGAGGCGCGGGTAACCTCTGGAGTAGGCCGAGGCGGGGGGC A G ESCO2 Ensembl:ENSG00000171320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:27774577..27774657;chr8:27774597..27774685 26863196 MeRIP-seq:(Medium) rs1020168984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995393 Human_Splice_Rec_961499,Human_Splice_Rec_961519 99429 RMVar_ID_99429 Human_SNP_ID_357170805 m1A Human chr8 + 27892174 27892174 27892174 AAAGAGACTGAGAGGCAGGGATGGTGGAATCAATAAGCCATGTTGGAGAAGAGGCCTCCCAGTGA AAAGAGACTGAGAGGCAGGGATGGTGGAATCAGTAAGCCATGTTGGAGAAGAGGCCTCCCAGTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27892129..27892232 26863196 MeRIP-seq:(Medium) rs1047112556 Functional Loss SNV dbSNP153 33..33 33 - - - 99430 RMVar_ID_99430 Human_SNP_ID_357194173 m1A Human chr8 - 27982001 27982001 27982001 ATAAAATGAAAATATCCTCCTCATCTACCTTCATATCCGTCAGATCTCCCCGGTTCACTTGGCGC ATAAAATGAAAATATCCTCCTCATCTACCTTCTTATCCGTCAGATCTCCCCGGTTCACTTGGCGC T A SCARA5 Ensembl:ENSG00000168079 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27981951..27982307 26863196 MeRIP-seq:(Medium) rs1442315485 Functional Loss SNV dbSNP153 33..33 33 - - - 99431 RMVar_ID_99431 Human_SNP_ID_357227679 m1A Human chr8 + 28115113 28115113 28115113 CTGTATACTGAGGTGGGAAAGATAGCGGGAAGAGCAGAGAAAATCTCAGAGGGAGAAAATCAAGA CTGTATACTGAGGTGGGAAAGATAGCGGGAAGTGCAGAGAAAATCTCAGAGGGAGAAAATCAAGA A T ELP3 Ensembl:ENSG00000134014 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28114934..28115127 26863196 MeRIP-seq:(Medium) rs1563254383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250966,RMVar_hsa_circ_6839,RMVar_hsa_circ_1187,RMVar_hsa_circ_324756,RMVar_hsa_circ_43074,RMVar_hsa_circ_318899,RMVar_hsa_circ_363603,RMVar_hsa_circ_250967,RMVar_hsa_circ_76638,RMVar_hsa_circ_30033,RMVar_hsa_circ_250972,RMVar_hsa_circ_109233,RMVar_hsa_circ_375115,RMVar_hsa_circ_250974,RMVar_hsa_circ_335194,RMVar_hsa_circ_343754,RMVar_hsa_circ_250975,RMVar_hsa_circ_70651 99432 RMVar_ID_99432 Human_SNP_ID_357231323 m1A Human chr8 - 28130736 28130736 28130736 CAATCTTCCTCTTCTGCACCTGACCAACTCAGACTCTTCCATGAAGTCCCAACTCAGATGTCGTA CAATCTTCCTCTTCTGCACCTGACCAACTCAGTCTCTTCCATGAAGTCCCAACTCAGATGTCGTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28130734..28130859 26863196 MeRIP-seq:(Medium) rs1055622918 Functional Loss SNV dbSNP153 33..33 33 - - - 99433 RMVar_ID_99433 Human_SNP_ID_357231324 m1A Human chr8 - 28130736 28130736 28130736 CAATCTTCCTCTTCTGCACCTGACCAACTCAGACTCTTCCATGAAGTCCCAACTCAGATGTCGTA CAATCTTCCTCTTCTGCACCTGACCAACTCAGCCTCTTCCATGAAGTCCCAACTCAGATGTCGTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28130734..28130859 26863196 MeRIP-seq:(Medium) rs1055622918 Functional Loss SNV dbSNP153 33..33 33 - - - 99434 RMVar_ID_99434 Human_SNP_ID_357283844 m1A Human chr8 - 28348674 28348674 28348674 GTTCTACTCTGTTCCTGGCCCTGCCGGCAGCCACTGACAAGAGGCCAGTGTGTCACCAGCCCTCA GTTCTACTCTGTTCCTGGCCCTGCCGGCAGCCGCTGACAAGAGGCCAGTGTGTCACCAGCCCTCA T C ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:28348568..28348684 32194978 MeRIP-seq:(Medium) rs1473327024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959007,Human_RBP_ID_9406169 99435 RMVar_ID_99435 Human_SNP_ID_357287287 m1A Human chr8 - 28361136 28361136 28361136 CTTCAGTGTCCCCTTCGCCTCCGCAGGAGAGGAGAGGCAGCAGCATGGCGAGTGTCCTGTCCCGA CTTCAGTGTCCCCTTCGCCTCCGCAGGAGAGGTGAGGCAGCAGCATGGCGAGTGTCCTGTCCCGA T A ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28361009..28365360 26863196 MeRIP-seq:(Medium) rs552906719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994964 Human_Splice_Rec_962032,Human_Splice_Rec_962052,Human_Splice_Rec_962070,Human_Splice_Rec_962092,Human_Splice_Rec_962100,Human_Splice_Rec_962106,Human_Splice_Rec_962110,Human_Splice_Rec_962114,Human_Splice_Rec_962132 RMVar_hsa_circ_250981,RMVar_hsa_circ_370258,RMVar_hsa_circ_4566,RMVar_hsa_circ_87906,RMVar_hsa_circ_357512,RMVar_hsa_circ_338425,RMVar_hsa_circ_250983,RMVar_hsa_circ_307509 99436 RMVar_ID_99436 Human_SNP_ID_357292824 m1A Human chr8 - 28384091 28384091 28384091 AGTGAGCAGGCTGTTGGAGTTGCAGGGTGGCCAGAGTTTGCACTGGGATCACTGGAAGTGAAAAA AGTGAGCAGGCTGTTGGAGTTGCAGGGTGGCCGGAGTTTGCACTGGGATCACTGGAAGTGAAAAA T C ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28384089..28384223 26863196 MeRIP-seq:(Medium) rs1313568751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 99437 RMVar_ID_99437 Human_SNP_ID_357292888 m1A Human chr8 - 28384324 28384324 28384324 CTTTCCAGAGAGACAAGGAGATGTCCTTAGCCATACCAGGGAATGTATCCTGAACAGTAGGAGAT CTTTCCAGAGAGACAAGGAGATGTCCTTAGCCGTACCAGGGAATGTATCCTGAACAGTAGGAGAT T C ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28384322..28384470 26863196 MeRIP-seq:(Medium) rs751611087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 99438 RMVar_ID_99438 Human_SNP_ID_357292970 m1A Human chr8 + 28384634 28384634 28384634 GAGACAGGTATGAGCCTCTGCTCCTCTGCTCCACTTTGTAAATTATCCCACCTGTTACTTTCTTC GAGACAGGTATGAGCCTCTGCTCCTCTGCTCCTCTTTGTAAATTATCCCACCTGTTACTTTCTTC A T RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28384630..28384714 26863196 MeRIP-seq:(Medium) rs1276602008 Functional Loss SNV dbSNP153 33..33 33 - - - 99439 RMVar_ID_99439 Human_SNP_ID_357293492 m1A Human chr8 + 28386156 28386156 28386156 CCGCGGCCCGGCTCCGCTCCGGCCGCCCGCCGAGGCTCGGTTGGCGCCCACCTGGCCGGCCTGCC CCGCGGCCCGGCTCCGCTCCGGCCGCCCGCCGGGGCTCGGTTGGCGCCCACCTGGCCGGCCTGCC A G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr8:28386012..28386404;chr8:28386061..28386188;chr8:28385926..28386431 26863196 MeRIP-seq:(Medium) rs890530774 Functional Loss SNV dbSNP153 33..33 33 - - - 99440 RMVar_ID_99440 Human_SNP_ID_357318532 m1A Human chr8 - 28483395 28483395 28483395 CAAAAAACACAGATGGTCCCAAAATGCAGACAAAGATGAGCACCTGGACACCCCTAAACCATCAG CAAAAAACACAGATGGTCCCAAAATGCAGACAGAGATGAGCACCTGGACACCCCTAAACCATCAG T C FBXO16 Ensembl:ENSG00000214050 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28483347..28483448 26863196 MeRIP-seq:(Medium) rs1179968911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_962120,Human_Splice_Rec_962121,Human_Splice_Rec_962154,Human_Splice_Rec_962155,Human_Splice_Rec_962172,Human_Splice_Rec_962173,Human_Splice_Rec_962184,Human_Splice_Rec_962185,Human_Splice_Rec_962210,Human_Splice_Rec_962211,Human_Splice_Rec_962221 RMVar_hsa_circ_77970,RMVar_hsa_circ_87906,RMVar_hsa_circ_250983,RMVar_hsa_circ_250984,RMVar_hsa_circ_250991,RMVar_hsa_circ_42511 99441 RMVar_ID_99441 Human_SNP_ID_357354178 m1A Human chr8 + 28630738 28630738 28630738 TTAGGAGCAGAACAGGTAAGGATGGGTAAGACATGGTGCCTGCCATTGAGAGGCTTATAACTGGG TTAGGAGCAGAACAGGTAAGGATGGGTAAGACGTGGTGCCTGCCATTGAGAGGCTTATAACTGGG A G EXTL3 Ensembl:ENSG00000012232 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28630732..28630913 26863196 MeRIP-seq:(Medium) rs1343953312 Functional Loss SNV dbSNP153 33..33 33 - - - 99442 RMVar_ID_99442 Human_SNP_ID_357354201 m1A Human chr8 - 28630806 28630806 28630806 TATGCATTTCCAGCAAAGTTCTTTGACACCTCACCCACTTGTCTATCTACGTGTCTGTCTTCCTC TATGCATTTCCAGCAAAGTTCTTTGACACCTCTCCCACTTGTCTATCTACGTGTCTGTCTTCCTC T A RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:28630704..28630833 26863196 MeRIP-seq:(Medium) rs1257416258 Functional Loss SNV dbSNP153 33..33 33 - - - 99443 RMVar_ID_99443 Human_SNP_ID_357370529 m1A Human chr8 + 28699352 28699350 28699352 AGAGTGTGAGAAGGAAAAAAGAAAGTAGCCCCAGTCATATCATTGGCAGAGAACACAAGGTAGGA AGAGTGTGAGAAGGAAAAAAGAAAGTAGCCC__GTCATATCATTGGCAGAGAACACAAGGTAGGA CCA C EXTL3 Ensembl:ENSG00000012232 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28699347..28699478 26863196 MeRIP-seq:(Medium) rs1211110604 Functional Loss DEL dbSNP153 32..33 33 - - - 99444 RMVar_ID_99444 Human_SNP_ID_357370530 m1A Human chr8 + 28699352 28699352 28699352 AGAGTGTGAGAAGGAAAAAAGAAAGTAGCCCCAGTCATATCATTGGCAGAGAACACAAGGTAGGA AGAGTGTGAGAAGGAAAAAAGAAAGTAGCCCCGGTCATATCATTGGCAGAGAACACAAGGTAGGA A G EXTL3 Ensembl:ENSG00000012232 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28699347..28699478 26863196 MeRIP-seq:(Medium) rs1461114543 Functional Loss SNV dbSNP153 33..33 33 - - - 99445 RMVar_ID_99445 Human_SNP_ID_357371190 m1A Human chr8 + 28701566 28701566 28701566 GCAGGGGGAGCGGCGGATCAGGCGCGGCCTGGAAGGCGGGCGGCCGGCAGCCAGAACGGCTTCTG GCAGGGGGAGCGGCGGATCAGGCGCGGCCTGGCAGGCGGGCGGCCGGCAGCCAGAACGGCTTCTG A C EXTL3 Ensembl:ENSG00000012232 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:28701516..28701703 26863196 MeRIP-seq:(Medium) rs925150068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255231,Human_RBP_ID_4994966 Human_Splice_Rec_962303,Human_Splice_Rec_962315 99446 RMVar_ID_99446 Human_SNP_ID_357374963 m1A Human chr8 + 28716528 28716528 28716528 TGGCCCAGAACCAGCCCAAGCTGTCCCTGCCCATCCGACTGCTCCCAGAGAAGGACGATGCCGGC TGGCCCAGAACCAGCCCAAGCTGTCCCTGCCCGTCCGACTGCTCCCAGAGAAGGACGATGCCGGC A G EXTL3 Ensembl:ENSG00000012232 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:28716477..28716578 32194978 MeRIP-seq:(Medium) rs1366627170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4981870,Human_RBP_ID_8918822,Human_RBP_ID_27537917 Human_miRNA_ID_2424079,Human_miRNA_ID_2433739,Human_miRNA_ID_3117220 RMVar_hsa_circ_81583,RMVar_hsa_circ_117303,RMVar_hsa_circ_92221,RMVar_hsa_circ_52970,RMVar_hsa_circ_251011,RMVar_hsa_circ_305751,RMVar_hsa_circ_251007,RMVar_hsa_circ_251008,RMVar_hsa_circ_375789,RMVar_hsa_circ_251006,RMVar_hsa_circ_370817,RMVar_hsa_circ_285657,RMVar_hsa_circ_251012,RMVar_hsa_circ_251013,RMVar_hsa_circ_251010,RMVar_hsa_circ_90374,RMVar_hsa_circ_287019,RMVar_hsa_circ_251014,RMVar_hsa_circ_251015,RMVar_hsa_circ_251016 99447 RMVar_ID_99447 Human_SNP_ID_357391015 m1A Human chr8 + 28778068 28778068 28778068 CCCACAGACAGTCAGGGGGTCAGGAGGGAGCCAGGAAGCACACGTGGGGGACGGAGGTCAAAGGG CCCACAGACAGTCAGGGGGTCAGGAGGGAGCCCGGAAGCACACGTGGGGGACGGAGGTCAAAGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28778019..28778199 26863196 MeRIP-seq:(Medium) rs1337545851 Functional Loss SNV dbSNP153 33..33 33 - - - 99448 RMVar_ID_99448 Human_SNP_ID_357417349 m1A Human chr8 - 28889914 28889914 28889914 ACCGGAAGACGCTTCCTGGGTTTGAGGAGTTCAGTGACTGCTATTGAACCACCAAAAGTCCATTA ACCGGAAGACGCTTCCTGGGTTTGAGGAGTTCGGTGACTGCTATTGAACCACCAAAAGTCCATTA T C INTS9 Ensembl:ENSG00000104299 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:28889845..28889928 26863196 MeRIP-seq:(Medium) rs1384572160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4982107,Human_RBP_ID_18895627 Human_Splice_Rec_962371,Human_Splice_Rec_962403,Human_Splice_Rec_962435,Human_Splice_Rec_962465,Human_Splice_Rec_962501,Human_Splice_Rec_962551,Human_Splice_Rec_962569,Human_Splice_Rec_962585,Human_Splice_Rec_962619,Human_Splice_Rec_962629 RMVar_hsa_circ_251037,RMVar_hsa_circ_85135 99449 RMVar_ID_99449 Human_SNP_ID_357417424 m1A Human chr8 - 28890104 28890104 28890104 GGCGGCTGGGATGAATTTGAGCTGACGGAAGGAGGCGTTCGGAGAGGAAAGGGAGGAAAAGGAAA GGCGGCTGGGATGAATTTGAGCTGACGGAAGGTGGCGTTCGGAGAGGAAAGGGAGGAAAAGGAAA T A INTS9 Ensembl:ENSG00000104299 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:28890034..28890160 26863196 MeRIP-seq:(Medium) rs1183041433 Functional Loss SNV dbSNP153 33..33 33 - - - 99450 RMVar_ID_99450 Human_SNP_ID_357458908 m1A Human chr8 - 29067923 29067923 29067923 CACTGCGTCCAGCAGCAGAGGGGACAGGGGGCAGGTGTGTGACTGGGTTCCTGGGTACCCAGGCC CACTGCGTCCAGCAGCAGAGGGGACAGGGGGCGGGTGTGTGACTGGGTTCCTGGGTACCCAGGCC T C KIF13B Ensembl:ENSG00000197892 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:29067876..29067948 26863196 MeRIP-seq:(Medium) rs1563671272 Functional Loss SNV dbSNP153 33..33 33 - - - 99451 RMVar_ID_99451 Human_SNP_ID_357468875 m1A Human chr8 + 29104317 29104317 29104317 TTCATCTCTCGGACCTATACACTGCTGTCCAAAACCCGATGTCACCCAAGTCCCCTCACTCCAGC TTCATCTCTCGGACCTATACACTGCTGTCCAATACCCGATGTCACCCAAGTCCCCTCACTCCAGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:29104298..29104420 26863196 MeRIP-seq:(Medium) rs1205170131 Functional Loss SNV dbSNP153 33..33 33 - - - 99452 RMVar_ID_99452 Human_SNP_ID_357472050 m1A Human chr8 + 29115858 29115858 29115858 CGGAACTGCATCTCCTCCTACTATGCCTGGCCAATGCCCCTCCTCTCTAAGTCCCAGTTCAAACG CGGAACTGCATCTCCTCCTACTATGCCTGGCCTATGCCCCTCCTCTCTAAGTCCCAGTTCAAACG A T AC108449.1 Ensembl:ENSG00000254129 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:29115814..29115925 26863196 MeRIP-seq:(Medium) rs1248446580 Functional Loss SNV dbSNP153 33..33 33 - - - 99453 RMVar_ID_99453 Human_SNP_ID_357508277 m1A Human chr8 - 29258637 29258637 29258637 GAGGAGGAAGTATGGCCTGAGAGTGAGGACACAGAGACTAGAATGAGTAAAGCAGGTTTAGGCAG GAGGAGGAAGTATGGCCTGAGAGTGAGGACACGGAGACTAGAATGAGTAAAGCAGGTTTAGGCAG T C KIF13B Ensembl:ENSG00000197892 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:29258635..29258767 26863196 MeRIP-seq:(Medium) rs530844361 Functional Loss SNV dbSNP153 33..33 33 - - - 99454 RMVar_ID_99454 Human_SNP_ID_357508281 m1A Human chr8 + 29258652 29258652 29258652 TTACTCATTCTAGTCTCTGTGTCCTCACTCTCAGGCCATACTTCCTCCTCAAAGAATACATGCCA TTACTCATTCTAGTCTCTGTGTCCTCACTCTCGGGCCATACTTCCTCCTCAAAGAATACATGCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:29258649..29258723 26863196 MeRIP-seq:(Medium) rs1031940563 Functional Loss SNV dbSNP153 33..33 33 - - - 99455 RMVar_ID_99455 Human_SNP_ID_357531689 m1A Human chr8 + 29350519 29350519 29350519 TCGGGCGCCCAGCCGGGCGGCGCGCAGAGCGGAGGGGGAGGCGCCGGTGGAGGAGAGTGTGTTTA TCGGGCGCCCAGCCGGGCGGCGCGCAGAGCGGCGGGGGAGGCGCCGGTGGAGGAGAGTGTGTTTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:29350468..29350652 26863196 MeRIP-seq:(Medium) rs1158594514 Functional Loss SNV dbSNP153 33..33 33 - - - 99456 RMVar_ID_99456 Human_SNP_ID_150650108 m1A Human chr3 - 120045317 120045317 120045317 ACAGTAACTAGAGGCAAGGAGGCATGGAGGACAAGAAAGTTGAGTTTGAGAACAAAGAACAAGGA ACAGTAACTAGAGGCAAGGAGGCATGGAGGACGAGAAAGTTGAGTTTGAGAACAAAGAACAAGGA T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120045314..120045492 26863196 MeRIP-seq:(Medium) rs1163338789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14580249 RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 99457 RMVar_ID_99457 Human_SNP_ID_150661353 m1A Human chr3 - 120090855 120090855 120090855 ATAAGAACATAAGAACAGATGGAATTTGAGAAATAAGAGAAAGTTAGCTGATGGAGGGCAGAGGG ATAAGAACATAAGAACAGATGGAATTTGAGAAGTAAGAGAAAGTTAGCTGATGGAGGGCAGAGGG T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120090852..120091046 26863196 MeRIP-seq:(Medium) rs540968455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 99458 RMVar_ID_99458 Human_SNP_ID_150662042 m1A Human chr3 - 120093372 120093372 120093372 GCGGAGAGCTGCAAGCCGGTGCAGCAGCCTTCAGCTTTTGGCAGCATGAAAGTTAGCAGTGAGTA GCGGAGAGCTGCAAGCCGGTGCAGCAGCCTTCTGCTTTTGGCAGCATGAAAGTTAGCAGTGAGTA T A GSK3B Ensembl:ENSG00000082701 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:120002215..120093483 26863196 MeRIP-seq:(Medium) rs760378387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_308753,Human_RBP_ID_937896,Human_RBP_ID_5530610,Human_RBP_ID_22091823,Human_RBP_ID_26347091 Human_Splice_Rec_471515,Human_Splice_Rec_471535,Human_Splice_Rec_471563 Human_miRNA_ID_2405530,Human_miRNA_ID_2408525,Human_miRNA_ID_2411516,Human_miRNA_ID_2414495,Human_miRNA_ID_2623005 RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 99459 RMVar_ID_99459 Human_SNP_ID_150662043 m1A Human chr3 - 120093372 120093372 120093372 GCGGAGAGCTGCAAGCCGGTGCAGCAGCCTTCAGCTTTTGGCAGCATGAAAGTTAGCAGTGAGTA GCGGAGAGCTGCAAGCCGGTGCAGCAGCCTTCGGCTTTTGGCAGCATGAAAGTTAGCAGTGAGTA T C GSK3B Ensembl:ENSG00000082701 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:120002215..120093483 26863196 MeRIP-seq:(Medium) rs760378387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_308753,Human_RBP_ID_937896,Human_RBP_ID_5530610,Human_RBP_ID_22091823,Human_RBP_ID_26347091 Human_Splice_Rec_471515,Human_Splice_Rec_471535,Human_Splice_Rec_471563 Human_miRNA_ID_2405530,Human_miRNA_ID_2408525,Human_miRNA_ID_2411516,Human_miRNA_ID_2414495,Human_miRNA_ID_2623005 RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 99460 RMVar_ID_99460 Human_SNP_ID_150662062 m1A Human chr3 - 120093446 120093446 120093446 AAAAGGAGGAAGGAAGGAAAAGGTGATTCGCGAAGAGAGTGATCATGTCAGGGCGGCCCAGAACC AAAAGGAGGAAGGAAGGAAAAGGTGATTCGCGGAGAGAGTGATCATGTCAGGGCGGCCCAGAACC T C GSK3B Ensembl:ENSG00000082701 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:120093326..120093500 26863196 MeRIP-seq:(Medium) rs758244414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_937897,Human_RBP_ID_5206852,Human_RBP_ID_14581228 Human_Splice_Rec_471515,Human_Splice_Rec_471535,Human_Splice_Rec_471563 RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 99461 RMVar_ID_99461 Human_SNP_ID_150662070 m1A Human chr3 + 120093451 120093451 120093451 TGGGCCGCCCTGACATGATCACTCTCTTCGCGAATCACCTTTTCCTTCCTTCCTCCTTTTCTTCC TGGGCCGCCCTGACATGATCACTCTCTTCGCGGATCACCTTTTCCTTCCTTCCTCCTTTTCTTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:120093326..120093500 26863196 MeRIP-seq:(Medium) rs376366660 Functional Loss SNV dbSNP153 33..33 33 - - - 99462 RMVar_ID_99462 Human_SNP_ID_150662294 m1A Human chr3 + 120093962 120093961 120093962 GGAGATGCGACGGGAAACGCTGCAGCTCCGGCAAGCCGCGGGATCCGGCGGGCTGACGGCAGGGG GGAGATGCGACGGGAAACGCTGCAGCTCCGGC_AGCCGCGGGATCCGGCGGGCTGACGGCAGGGG CA C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:120093851..120093975 26863196 MeRIP-seq:(Medium) rs58853520 Functional Loss DEL dbSNP153 33..33 33 - - - 99463 RMVar_ID_99463 Human_SNP_ID_150662295 m1A Human chr3 + 120093962 120093962 120093962 GGAGATGCGACGGGAAACGCTGCAGCTCCGGCAAGCCGCGGGATCCGGCGGGCTGACGGCAGGGG GGAGATGCGACGGGAAACGCTGCAGCTCCGGCCAGCCGCGGGATCCGGCGGGCTGACGGCAGGGG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:120093851..120093975 26863196 MeRIP-seq:(Medium) rs1019374950 Functional Loss SNV dbSNP153 33..33 33 - - - 99464 RMVar_ID_99464 Human_SNP_ID_150662332 m1A Human chr3 - 120094020 120094020 120094020 CACCGCCACCGCCCGCCTCTGACTGACTCGCGACTCCGCCGCCCTCTAGTTCGCCGGGCCCCTGC CACCGCCACCGCCCGCCTCTGACTGACTCGCGGCTCCGCCGCCCTCTAGTTCGCCGGGCCCCTGC T C GSK3B Ensembl:ENSG00000082701 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:120093901..120094450 26863196 MeRIP-seq:(Medium) rs1160021121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1102538,Human_RBP_ID_14581245,Human_RBP_ID_22456085,Human_RBP_ID_22533923,Human_RBP_ID_27496987 RMVar_hsa_circ_264817 99465 RMVar_ID_99465 Human_SNP_ID_150662439 m1A Human chr3 - 120094248 120094248 120094248 CCGAGCAGAGCCGAGGGGCGGGAGGGCGGCCGAGCTGTTGCCGCGGACGGGGGAGGGGGCCCCGA CCGAGCAGAGCCGAGGGGCGGGAGGGCGGCCGTGCTGTTGCCGCGGACGGGGGAGGGGGCCCCGA T A GSK3B Ensembl:ENSG00000082701 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:120094201..120094400 26863196 MeRIP-seq:(Medium) rs1035188964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756652,Human_RBP_ID_22093109 RMVar_hsa_circ_264817 99466 RMVar_ID_99466 Human_SNP_ID_150662440 m1A Human chr3 - 120094248 120094248 120094248 CCGAGCAGAGCCGAGGGGCGGGAGGGCGGCCGAGCTGTTGCCGCGGACGGGGGAGGGGGCCCCGA CCGAGCAGAGCCGAGGGGCGGGAGGGCGGCCGGGCTGTTGCCGCGGACGGGGGAGGGGGCCCCGA T C GSK3B Ensembl:ENSG00000082701 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:120094201..120094400 26863196 MeRIP-seq:(Medium) rs1035188964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756652,Human_RBP_ID_22093109 RMVar_hsa_circ_264817 99467 RMVar_ID_99467 Human_SNP_ID_150662460 m1A Human chr3 - 120094305 120094305 120094305 GCAGCCGCTGACAGGGCTCTGGGCTGGGGCAAAGCGCGGACACTTCCTGAGCGGGCACCGAGCAG GCAGCCGCTGACAGGGCTCTGGGCTGGGGCAACGCGCGGACACTTCCTGAGCGGGCACCGAGCAG T G GSK3B Ensembl:ENSG00000082701 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:120093869..120094500 26863196 MeRIP-seq:(Medium) rs201519023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1615976,Human_RBP_ID_4758865,Human_RBP_ID_5473604,Human_RBP_ID_7108945,Human_RBP_ID_14581249,Human_RBP_ID_18794615,Human_RBP_ID_27496989 RMVar_hsa_circ_264817 99468 RMVar_ID_99468 Human_SNP_ID_150662521 m1A Human chr3 + 120094409 120094409 120094409 TTGGCCCGGGCGGCGGCGGCGGCGGCGGCGGCACAAGCCCGCATTCGCCCGGGTCAGGAGCTGCT TTGGCCCGGGCGGCGGCGGCGGCGGCGGCGGCGCAAGCCCGCATTCGCCCGGGTCAGGAGCTGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr3:120093843..120094500;chr3:120093885..120094501;chr3:120093897..120094500;chr3:120094305..120094450 26863196 MeRIP-seq:(Medium) rs1461758961 Functional Loss SNV dbSNP153 33..33 33 - - - 99469 RMVar_ID_99469 Human_SNP_ID_150662522 m1A Human chr3 + 120094409 120094409 120094409 TTGGCCCGGGCGGCGGCGGCGGCGGCGGCGGCACAAGCCCGCATTCGCCCGGGTCAGGAGCTGCT TTGGCCCGGGCGGCGGCGGCGGCGGCGGCGGCTCAAGCCCGCATTCGCCCGGGTCAGGAGCTGCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr3:120093843..120094500;chr3:120093885..120094501;chr3:120093897..120094500;chr3:120094305..120094450 26863196 MeRIP-seq:(Medium) rs1461758961 Functional Loss SNV dbSNP153 33..33 33 - - - 99470 RMVar_ID_99470 Human_SNP_ID_150715859 m1A Human chr3 - 120327119 120327119 120327119 TTAAAATTAAGTTATTGAGTGGCCTACTGACTACCATCCAAAAACCTTTATCACCAAATTTGTTC TTAAAATTAAGTTATTGAGTGGCCTACTGACTGCCATCCAAAAACCTTTATCACCAAATTTGTTC T C LRRC58 Ensembl:ENSG00000163428 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11554681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17516610,Human_RBP_ID_17992103 Human_miRNA_ID_88795,Human_miRNA_ID_1956410 GWAS_ID_13119,GWAS_ID_13120,GWAS_ID_13121,GWAS_ID_13122,GWAS_ID_13123,GWAS_ID_13124 RMVar_hsa_circ_86357,RMVar_hsa_circ_220525 99471 RMVar_ID_99471 Human_SNP_ID_150716632 m1A Human chr3 - 120330270 120330270 120330270 GGTAGGCCACAATCTTCATCAATCTGTTCATCATAAGACAGAGTAAGAATTTTTAACAGAAAATT GGTAGGCCACAATCTTCATCAATCTGTTCATCGTAAGACAGAGTAAGAATTTTTAACAGAAAATT T C LRRC58 Ensembl:ENSG00000163428 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6438575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1030530,Human_RBP_ID_2742997,Human_RBP_ID_14581533,Human_RBP_ID_17287867,Human_RBP_ID_17401311,Human_RBP_ID_17516638,Human_RBP_ID_17992141,Human_RBP_ID_27312038 GWAS_ID_13125 RMVar_hsa_circ_86357,RMVar_hsa_circ_220525 99472 RMVar_ID_99472 Human_SNP_ID_150721216 m1A Human chr3 + 120349189 120349189 120349189 CTCCAGCGTCTCGGTGGACACGCTGAGGCGGGACCAGTTCAGTTCGGCCTCCCCGGCCGTGACCA CTCCAGCGTCTCGGTGGACACGCTGAGGCGGGCCCAGTTCAGTTCGGCCTCCCCGGCCGTGACCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:120349138..120349317 26863196 MeRIP-seq:(Medium) rs1228093044 Functional Loss SNV dbSNP153 33..33 33 - - - 99473 RMVar_ID_99473 Human_SNP_ID_150721232 m1A Human chr3 - 120349226 120349226 120349226 CGTGCGGTGGCCAGGATGGAGGAGGCCGGAGCAGCGGTGGTCACGGCCGGGGAGGCCGAACTGAA CGTGCGGTGGCCAGGATGGAGGAGGCCGGAGCGGCGGTGGTCACGGCCGGGGAGGCCGAACTGAA T C LRRC58 Ensembl:ENSG00000163428 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:120349176..120349359 26863196 MeRIP-seq:(Medium) rs1399680710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247524,Human_RBP_ID_783639,Human_RBP_ID_4718105,Human_RBP_ID_8943493 RMVar_hsa_circ_220527,RMVar_hsa_circ_120010 99474 RMVar_ID_99474 Human_SNP_ID_150731384 m1A Human chr3 + 120394386 120394386 120394386 TATAGAAGCCTACTAAATACAAATACAAGTTCACAAACACATATGCAACAGAAACTTGTTTAGAT TATAGAAGCCTACTAAATACAAATACAAGTTCCCAAACACATATGCAACAGAAACTTGTTTAGAT A C AC063952.1 Ensembl:ENSG00000240661 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:120394336..120394487 32194978 MeRIP-seq:(Medium) rs750563045 Functional Loss SNV dbSNP153 33..33 33 - - - 99475 RMVar_ID_99475 Human_SNP_ID_150731543 m1A Human chr3 - 120395117 120395117 120395117 CTCATTTGAAAGGAGAAAATTCCACTTTGTTTAGCATTTCAAGCTTTTATGTATCCATCCCATCT CTCATTTGAAAGGAGAAAATTCCACTTTGTTTGGCATTTCAAGCTTTTATGTATCCATCCCATCT T C FSTL1 Ensembl:ENSG00000163430 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:120394801..120395125 32194978 MeRIP-seq:(Medium) rs137890311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1616073,Human_RBP_ID_1947136,Human_RBP_ID_3682991,Human_RBP_ID_4759970,Human_RBP_ID_17516681,Human_RBP_ID_17702593,Human_RBP_ID_18331768,Human_RBP_ID_22397214,Human_RBP_ID_23016988 Human_miRNA_ID_1281044 99476 RMVar_ID_99476 Human_SNP_ID_150732622 m1A Human chr3 - 120399961 120399961 120399961 CTGCTACTGCTCTGAGCTTTGGTTCTTCTTGCAGGAAAGAATCAGAAGGGGGCCCAGACCCAGAC CTGCTACTGCTCTGAGCTTTGGTTCTTCTTGCTGGAAAGAATCAGAAGGGGGCCCAGACCCAGAC T A FSTL1 Ensembl:ENSG00000163430 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:120399926..120399975 26863196 MeRIP-seq:(Medium) rs751186231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_471709,Human_Splice_Rec_471729,Human_Splice_Rec_471731 RMVar_hsa_circ_114707,RMVar_hsa_circ_320961,RMVar_hsa_circ_220531 99477 RMVar_ID_99477 Human_SNP_ID_150732623 m1A Human chr3 - 120399961 120399961 120399961 CTGCTACTGCTCTGAGCTTTGGTTCTTCTTGCAGGAAAGAATCAGAAGGGGGCCCAGACCCAGAC CTGCTACTGCTCTGAGCTTTGGTTCTTCTTGCGGGAAAGAATCAGAAGGGGGCCCAGACCCAGAC T C FSTL1 Ensembl:ENSG00000163430 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:120399926..120399975 26863196 MeRIP-seq:(Medium) rs751186231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_471709,Human_Splice_Rec_471729,Human_Splice_Rec_471731 RMVar_hsa_circ_114707,RMVar_hsa_circ_320961,RMVar_hsa_circ_220531 99478 RMVar_ID_99478 Human_SNP_ID_150733214 m1A Human chr3 + 120402836 120402836 120402836 TCACCGTCACAGGTCATGGCTGTACAGACCCAATTTCCACAGGCACAGACACAGCGGTTACAGTC TCACCGTCACAGGTCATGGCTGTACAGACCCAGTTTCCACAGGCACAGACACAGCGGTTACAGTC A G AC063952.1 Ensembl:ENSG00000240661 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:120402801..120402975 32194978 MeRIP-seq:(Medium) rs1560010936 Functional Loss SNV dbSNP153 33..33 33 - - - 99479 RMVar_ID_99479 Human_SNP_ID_150733348 m1A Human chr3 - 120403264 120403264 120403264 AGCTTCCAAGAGTTTCTCAAGTGCCTCAACCCATCTTTCAACCCTCCTGAGAAGAGTATGCCTAA AGCTTCCAAGAGTTTCTCAAGTGCCTCAACCCGTCTTTCAACCCTCCTGAGAAGAGTATGCCTAA T C FSTL1 Ensembl:ENSG00000163430 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:120403255..120410007 32194978 MeRIP-seq:(Medium) rs1433737084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68231,Human_RBP_ID_3683005,Human_RBP_ID_7109405,Human_RBP_ID_8556251,Human_RBP_ID_17702612,Human_RBP_ID_17992205,Human_RBP_ID_18210030,Human_RBP_ID_23286422,Human_RBP_ID_27497057 Human_Splice_Rec_471704,Human_Splice_Rec_471705,Human_Splice_Rec_471711,Human_Splice_Rec_471724,Human_Splice_Rec_471725 Human_miRNA_ID_2293578 RMVar_hsa_circ_28097,RMVar_hsa_circ_320961,RMVar_hsa_circ_102636,RMVar_hsa_circ_111771,RMVar_hsa_circ_92514,RMVar_hsa_circ_220533,RMVar_hsa_circ_220534,RMVar_hsa_circ_102788,RMVar_hsa_circ_220535,RMVar_hsa_circ_220536 99480 RMVar_ID_99480 Human_SNP_ID_150738463 m1A Human chr3 + 120423480 120423480 120423480 GAAACATGTTAGGCCTGTTCATATAGGGCTGAAAATCATCTCACAAAGATCTGTGAGGCTCAGGG GAAACATGTTAGGCCTGTTCATATAGGGCTGAGAATCATCTCACAAAGATCTGTGAGGCTCAGGG A G AC063952.1 Ensembl:ENSG00000240661 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:120423478..120423578 32194978 MeRIP-seq:(Medium) rs1004882036 Functional Loss SNV dbSNP153 33..33 33 - - - 99481 RMVar_ID_99481 Human_SNP_ID_150741264 m1A Human chr3 - 120435324 120435324 120435324 GTTAAGCAAATGCAGATGAGGCAATTGAGTGAAGAATTTCTGTTAAGTGCTTCATGAGAAAATAC GTTAAGCAAATGCAGATGAGGCAATTGAGTGAGGAATTTCTGTTAAGTGCTTCATGAGAAAATAC T C FSTL1 Ensembl:ENSG00000163430 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120435321..120435484 26863196 MeRIP-seq:(Medium) rs749464812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102636,RMVar_hsa_circ_220534,RMVar_hsa_circ_39445 99482 RMVar_ID_99482 Human_SNP_ID_150741265 m1A Human chr3 - 120435324 120435324 120435324 GTTAAGCAAATGCAGATGAGGCAATTGAGTGAAGAATTTCTGTTAAGTGCTTCATGAGAAAATAC GTTAAGCAAATGCAGATGAGGCAATTGAGTGACGAATTTCTGTTAAGTGCTTCATGAGAAAATAC T G FSTL1 Ensembl:ENSG00000163430 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120435321..120435484 26863196 MeRIP-seq:(Medium) rs749464812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102636,RMVar_hsa_circ_220534,RMVar_hsa_circ_39445 99483 RMVar_ID_99483 Human_SNP_ID_150744707 m1A Human chr3 - 120450362 120450362 120450362 CTGGAGCAGCAGCGAGTTCAAAAAGGCGCCTCAGTTCCGTCCTTCACTTCAGAGGAGACTGAGAG CTGGAGCAGCAGCGAGTTCAAAAAGGCGCCTCGGTTCCGTCCTTCACTTCAGAGGAGACTGAGAG T C FSTL1 Ensembl:ENSG00000163430 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120450360..120450566 26863196 MeRIP-seq:(Medium) rs1470597111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102636,RMVar_hsa_circ_220534,RMVar_hsa_circ_39445 99484 RMVar_ID_99484 Human_SNP_ID_150744927 m1A Human chr3 + 120450842 120450842 120450842 CTCGGGTCCCGCAGGCTCGCTCCGGCCGCCCAAGCACCCCCGGCCGCCCGAAGAGTCCGGCCTCC CTCGGGTCCCGCAGGCTCGCTCCGGCCGCCCATGCACCCCCGGCCGCCCGAAGAGTCCGGCCTCC A T AC126182.3 Ensembl:ENSG00000286735 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:120450832..120450975 26863410 MeRIP-seq:(Medium) rs1185908255 Functional Loss SNV dbSNP153 33..33 33 - - - 99485 RMVar_ID_99485 Human_SNP_ID_150744951 m1A Human chr3 - 120450918 120450918 120450918 AGCTCGCTGCCGCCGTCCTGCCCCGCGCCCCCAGGAGACCTGGACCAGACCACGGTGAGCGCAGG AGCTCGCTGCCGCCGTCCTGCCCCGCGCCCCCGGGAGACCTGGACCAGACCACGGTGAGCGCAGG T C FSTL1 Ensembl:ENSG00000163430 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:120450901..120451000 32194978 MeRIP-seq:(Medium) rs986617527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247529,Human_RBP_ID_4718269,Human_RBP_ID_7109506 Human_Splice_Rec_471691,Human_Splice_Rec_471713,Human_Splice_Rec_471737,Human_Splice_Rec_471747,Human_Splice_Rec_471755,Human_Splice_Rec_471759,Human_Splice_Rec_471763 Human_miRNA_ID_2038943,Human_miRNA_ID_3017923 RMVar_hsa_circ_102636,RMVar_hsa_circ_220534,RMVar_hsa_circ_39445 99486 RMVar_ID_99486 Human_SNP_ID_150778261 m1A Human chr3 - 120596400 120596399 120596400 TGTTGTATTCGGCTGGGTCGAGGGTCTCAGGCAGAGTGCGCAGGCTCGACGGCTTATACTTTGGG TGTTGTATTCGGCTGGGTCGAGGGTCTCAGGC_GAGTGCGCAGGCTCGACGGCTTATACTTTGGG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120596351..120596483 26863196 MeRIP-seq:(Medium) rs762946713 Functional Loss DEL dbSNP153 33..33 33 - - - 99487 RMVar_ID_99487 Human_SNP_ID_150778262 m1A Human chr3 - 120596400 120596400 120596400 TGTTGTATTCGGCTGGGTCGAGGGTCTCAGGCAGAGTGCGCAGGCTCGACGGCTTATACTTTGGG TGTTGTATTCGGCTGGGTCGAGGGTCTCAGGCGGAGTGCGCAGGCTCGACGGCTTATACTTTGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120596351..120596483 26863196 MeRIP-seq:(Medium) rs1177478058 Functional Loss SNV dbSNP153 33..33 33 - - - 99488 RMVar_ID_99488 Human_SNP_ID_150779388 m1A Human chr3 + 120601047 120601047 120601047 AAATGCGTCTGTGCTCCTTCACAAAAGTCCCTATGAATTTGTTTCTCAATGTGATCCTTCTTAAG AAATGCGTCTGTGCTCCTTCACAAAAGTCCCTGTGAATTTGTTTCTCAATGTGATCCTTCTTAAG A G NDUFB4 Ensembl:ENSG00000065518 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:120601045..120601131 26863196 MeRIP-seq:(Medium) rs942472425 Functional Loss SNV dbSNP153 33..33 33 - - - 99489 RMVar_ID_99489 Human_SNP_ID_150779390 m1A Human chr3 + 120601063 120601063 120601063 CTTCACAAAAGTCCCTATGAATTTGTTTCTCAATGTGATCCTTCTTAAGTTCTATAACTTTTTGT CTTCACAAAAGTCCCTATGAATTTGTTTCTCAGTGTGATCCTTCTTAAGTTCTATAACTTTTTGT A G NDUFB4 Ensembl:ENSG00000065518 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:120601060..120601146 26863196 MeRIP-seq:(Medium) rs369003915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17622028,Human_RBP_ID_25690215 99490 RMVar_ID_99490 Human_SNP_ID_150805514 m1A Human chr3 - 120709888 120709888 120709888 TGATTTGTTAGGTTCATGATTACAAAGAAGGAACCCCAGAAGAGAAGACCTACTACATAGAATTA TGATTTGTTAGGTTCATGATTACAAAGAAGGAGCCCCAGAAGAGAAGACCTACTACATAGAATTA T C RABL3 Ensembl:ENSG00000144840 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:120709837..120709952 26863196 MeRIP-seq:(Medium) rs1227939686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1616126,Human_RBP_ID_1947186,Human_RBP_ID_18535723,Human_RBP_ID_18794720,Human_RBP_ID_26347093 Human_Splice_Rec_471892,Human_Splice_Rec_471908,Human_Splice_Rec_471922,Human_Splice_Rec_471958,Human_Splice_Rec_471972,Human_Splice_Rec_471986,Human_Splice_Rec_471996 RMVar_hsa_circ_220548,RMVar_hsa_circ_96509,RMVar_hsa_circ_377824 99491 RMVar_ID_99491 Human_SNP_ID_150821963 m1A Human chr3 - 120774271 120774271 120774271 CTCACACCCATTTGTCTCTCTGACTCCTTTCAATGCCTCTTCTATCCTCAGCCAACATCCCCATC CTCACACCCATTTGTCTCTCTGACTCCTTTCAGTGCCTCTTCTATCCTCAGCCAACATCCCCATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:120774232..120774382 26863196 MeRIP-seq:(Medium) rs552506748 Functional Loss SNV dbSNP153 33..33 33 - - - 99492 RMVar_ID_99492 Human_SNP_ID_151038552 m1A Human chr3 - 121545948 121545948 121545948 AGACTGGCGGGAAGATGTCCGCAGCTGTTGCCAGGCCAGGGTTCTCCCGAGAGGGAGGACGCTGG AGACTGGCGGGAAGATGTCCGCAGCTGTTGCCGGGCCAGGGTTCTCCCGAGAGGGAGGACGCTGG T C POLQ Ensembl:ENSG00000051341 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:121545805..121545947 26863196 MeRIP-seq:(Medium) rs745872649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248086,Human_RBP_ID_5530613,Human_RBP_ID_18424043,Human_RBP_ID_19012867,Human_RBP_ID_22092463,Human_RBP_ID_22274502,Human_RBP_ID_25690962 99493 RMVar_ID_99493 Human_SNP_ID_151038553 m1A Human chr3 - 121545948 121545948 121545948 AGACTGGCGGGAAGATGTCCGCAGCTGTTGCCAGGCCAGGGTTCTCCCGAGAGGGAGGACGCTGG AGACTGGCGGGAAGATGTCCGCAGCTGTTGCCCGGCCAGGGTTCTCCCGAGAGGGAGGACGCTGG T G POLQ Ensembl:ENSG00000051341 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:121545805..121545947 26863196 MeRIP-seq:(Medium) rs745872649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248086,Human_RBP_ID_5530613,Human_RBP_ID_18424043,Human_RBP_ID_19012867,Human_RBP_ID_22092463,Human_RBP_ID_22274502,Human_RBP_ID_25690962 99494 RMVar_ID_99494 Human_SNP_ID_151061854 m1A Human chr3 + 121633096 121633096 121633096 TACCTCCGGGAGAGTCTGCCTAATGGGCAGCAAGGGCACTGGGTGTTCCCTGCTGGTTCTCACAG TACCTCCGGGAGAGTCTGCCTAATGGGCAGCAGGGGCACTGGGTGTTCCCTGCTGGTTCTCACAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:121631548..121643021 32194978 MeRIP-seq:(Medium) rs751853579 Functional Loss SNV dbSNP153 33..33 33 - - - 99495 RMVar_ID_99495 Human_SNP_ID_151065919 m1A Human chr3 + 121647446 121647446 121647446 GCTCCTCTGATACTTTGTTCCTCAGCTGGTGGATGCTGGAAGAAACCACATGACCAAGGCTCATC GCTCCTCTGATACTTTGTTCCTCAGCTGGTGGGTGCTGGAAGAAACCACATGACCAAGGCTCATC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:121647406..121653589 32194978 MeRIP-seq:(Medium) rs146539124 Functional Loss SNV dbSNP153 33..33 33 - - - 99496 RMVar_ID_99496 Human_SNP_ID_151085764 m1A Human chr3 - 121730965 121730961 121730965 TTTTCCCCCCTTCTTTTCCTACAGAAATGCTGAGCCGATTATCAGGATTAGCAAATGTTGTTTTG TTTTCCCCCCTTCTTTTCCTACAGAAATGCTG____GATTATCAGGATTAGCAAATGTTGTTTTG CGGCT C GOLGB1 Ensembl:ENSG00000173230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:121730915..121731022 26863196 MeRIP-seq:(Medium) rs764731462 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5206877,Human_RBP_ID_8867200,Human_RBP_ID_18424044,Human_RBP_ID_18794996 Human_Splice_Rec_472672,Human_Splice_Rec_472673,Human_Splice_Rec_472714,Human_Splice_Rec_472715,Human_Splice_Rec_472756,Human_Splice_Rec_472796,Human_Splice_Rec_472850,Human_Splice_Rec_472851,Human_Splice_Rec_472890,Human_Splice_Rec_472891 RMVar_hsa_circ_5882,RMVar_hsa_circ_343887,RMVar_hsa_circ_293533,RMVar_hsa_circ_220617,RMVar_hsa_circ_220620,RMVar_hsa_circ_338581,RMVar_hsa_circ_220622,RMVar_hsa_circ_281329,RMVar_hsa_circ_15524 99497 RMVar_ID_99497 Human_SNP_ID_151085768 m1A Human chr3 - 121730965 121730965 121730965 TTTTCCCCCCTTCTTTTCCTACAGAAATGCTGAGCCGATTATCAGGATTAGCAAATGTTGTTTTG TTTTCCCCCCTTCTTTTCCTACAGAAATGCTGGGCCGATTATCAGGATTAGCAAATGTTGTTTTG T C GOLGB1 Ensembl:ENSG00000173230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:121730915..121731022 26863196 MeRIP-seq:(Medium) rs771666605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5206877,Human_RBP_ID_8867200,Human_RBP_ID_18424044,Human_RBP_ID_18794996 Human_Splice_Rec_472672,Human_Splice_Rec_472673,Human_Splice_Rec_472714,Human_Splice_Rec_472715,Human_Splice_Rec_472756,Human_Splice_Rec_472796,Human_Splice_Rec_472850,Human_Splice_Rec_472851,Human_Splice_Rec_472890,Human_Splice_Rec_472891 RMVar_hsa_circ_5882,RMVar_hsa_circ_343887,RMVar_hsa_circ_293533,RMVar_hsa_circ_220617,RMVar_hsa_circ_220620,RMVar_hsa_circ_338581,RMVar_hsa_circ_220622,RMVar_hsa_circ_281329,RMVar_hsa_circ_15524 99498 RMVar_ID_99498 Human_SNP_ID_151085769 m1A Human chr3 + 121730970 121730970 121730970 CAACATTTGCTAATCCTGATAATCGGCTCAGCATTTCTGTAGGAAAAGAAGGGGGGAAAAAACCT CAACATTTGCTAATCCTGATAATCGGCTCAGCCTTTCTGTAGGAAAAGAAGGGGGGAAAAAACCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:121730938..121731034 26863196 MeRIP-seq:(Medium) rs893291217 Functional Loss SNV dbSNP153 33..33 33 - - - 99499 RMVar_ID_99499 Human_SNP_ID_151109258 m1A Human chr3 - 121831119 121831119 121831119 CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCATGTCCTCCCTGCCTGTGATATCCAGGAAATTC CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCTTGTCCTCCCTGCCTGTGATATCCAGGAAATTC T A IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7612301 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13126,GWAS_ID_13127,GWAS_ID_13128 99500 RMVar_ID_99500 Human_SNP_ID_151109259 m1A Human chr3 - 121831119 121831119 121831119 CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCATGTCCTCCCTGCCTGTGATATCCAGGAAATTC CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCGTGTCCTCCCTGCCTGTGATATCCAGGAAATTC T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7612301 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13126,GWAS_ID_13127,GWAS_ID_13128 99501 RMVar_ID_99501 Human_SNP_ID_151110138 m1A Human chr3 - 121834904 121834904 121834904 GGAGAGGGCCCCAGGGCGCCTACCAGGAGGCCAGGACCCCAGGCTCCTGGACGAAGTCAGCCGGC GGAGAGGGCCCCAGGGCGCCTACCAGGAGGCCGGGACCCCAGGCTCCTGGACGAAGTCAGCCGGC T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:121834901..121835002 26863196 MeRIP-seq:(Medium) rs993805476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5392071,Human_RBP_ID_19115990 99502 RMVar_ID_99502 Human_SNP_ID_151110139 m1A Human chr3 - 121834904 121834904 121834904 GGAGAGGGCCCCAGGGCGCCTACCAGGAGGCCAGGACCCCAGGCTCCTGGACGAAGTCAGCCGGC GGAGAGGGCCCCAGGGCGCCTACCAGGAGGCCCGGACCCCAGGCTCCTGGACGAAGTCAGCCGGC T G IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:121834901..121835002 26863196 MeRIP-seq:(Medium) rs993805476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5392071,Human_RBP_ID_19115990 99503 RMVar_ID_99503 Human_SNP_ID_151110299 m1A Human chr3 - 121835267 121835267 121835267 GCTGCGCTATTCATAATTACTCTCCTGCTTTGACTTTAACTCCGCCACCAGCGCTCACTATCTGC GCTGCGCTATTCATAATTACTCTCCTGCTTTGCCTTTAACTCCGCCACCAGCGCTCACTATCTGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:121835209..121835330;chr3:121835230..121835363 26863196 MeRIP-seq:(Medium) rs1247962374 Functional Loss SNV dbSNP153 33..33 33 - - - 99504 RMVar_ID_99504 Human_SNP_ID_151112670 m1A Human chr3 - 121844487 121844487 121844487 TGTTCACCTTCACCAACCTCAAGGTATCCTTCAGAAGAAGTGTCAATAGAAGCAGGTTTGAAGTC TGTTCACCTTCACCAACCTCAAGGTATCCTTCGGAAGAAGTGTCAATAGAAGCAGGTTTGAAGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:121844404..121844487 26863196 MeRIP-seq:(Medium) rs376595504 Functional Loss SNV dbSNP153 33..33 33 - - - 99505 RMVar_ID_99505 Human_SNP_ID_151241303 m1A Human chr3 + 122384252 122384252 122384252 CGTCCCCGGCGAAGTTCTGCGCTGGTCGGCGGAGTAGCAAGTGGCCATGGGGAGCCTCAGCGGTC CGTCCCCGGCGAAGTTCTGCGCTGGTCGGCGGCGTAGCAAGTGGCCATGGGGAGCCTCAGCGGTC A C FAM162A Ensembl:ENSG00000114023 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:122384201..122384300 32194978 MeRIP-seq:(Medium) rs753560564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_587363,Human_RBP_ID_1616338,Human_RBP_ID_4718877,Human_RBP_ID_19012875,Human_RBP_ID_22456090,Human_RBP_ID_22608545,Human_RBP_ID_23964227 Human_Splice_Rec_473395,Human_Splice_Rec_473405,Human_Splice_Rec_473413 99506 RMVar_ID_99506 Human_SNP_ID_151241304 m1A Human chr3 + 122384252 122384252 122384252 CGTCCCCGGCGAAGTTCTGCGCTGGTCGGCGGAGTAGCAAGTGGCCATGGGGAGCCTCAGCGGTC CGTCCCCGGCGAAGTTCTGCGCTGGTCGGCGGGGTAGCAAGTGGCCATGGGGAGCCTCAGCGGTC A G FAM162A Ensembl:ENSG00000114023 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:122384201..122384300 32194978 MeRIP-seq:(Medium) rs753560564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_587363,Human_RBP_ID_1616338,Human_RBP_ID_4718877,Human_RBP_ID_19012875,Human_RBP_ID_22456090,Human_RBP_ID_22608545,Human_RBP_ID_23964227 Human_Splice_Rec_473395,Human_Splice_Rec_473405,Human_Splice_Rec_473413 99507 RMVar_ID_99507 Human_SNP_ID_151241315 m1A Human chr3 + 122384278 122384278 122384278 CGGCGGAGTAGCAAGTGGCCATGGGGAGCCTCAGCGGTCTGCGCCTGGCAGCAGGTGAGACGCCG CGGCGGAGTAGCAAGTGGCCATGGGGAGCCTCGGCGGTCTGCGCCTGGCAGCAGGTGAGACGCCG A G FAM162A Ensembl:ENSG00000114023 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:122384201..122384353;chr3:122384231..122384366 26863196 MeRIP-seq:(Medium) rs1476366520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_587365,Human_RBP_ID_4756659,Human_RBP_ID_5325630,Human_RBP_ID_17661507,Human_RBP_ID_19012875,Human_RBP_ID_22456090,Human_RBP_ID_22608546 Human_Splice_Rec_473395,Human_Splice_Rec_473405,Human_Splice_Rec_473413 99508 RMVar_ID_99508 Human_SNP_ID_151245394 m1A Human chr3 + 122402761 122402761 122402761 TTTCTTTGAAACATTTTCCTCTCTTTTTTAGGAAGCTGTTTTAGGTTATGTGAAAGAGATGTTTC TTTCTTTGAAACATTTTCCTCTCTTTTTTAGGCAGCTGTTTTAGGTTATGTGAAAGAGATGTTTC A C FAM162A Ensembl:ENSG00000114023 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1394411906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_935744,Human_RBP_ID_4756660,Human_RBP_ID_8943494,Human_RBP_ID_17064076,Human_RBP_ID_22274606,Human_RBP_ID_22456091,Human_RBP_ID_22551748,Human_RBP_ID_26347132,Human_RBP_ID_27043655 Human_Splice_Rec_473398,Human_Splice_Rec_473406,Human_Splice_Rec_473414 99509 RMVar_ID_99509 Human_SNP_ID_151268924 m1A Human chr3 - 122496569 122496569 122496569 CTCATTTGTTCTCTCCCCACTTGTATTGTAGAAATCATGACCACCCCAGGAAAAGAGAACTTTCG CTCATTTGTTCTCTCCCCACTTGTATTGTAGAGATCATGACCACCCCAGGAAAAGAGAACTTTCG T C KPNA1 Ensembl:ENSG00000114030 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:122496526..122496632 26863410 MeRIP-seq:(Medium) rs755460449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_473438,Human_Splice_Rec_473532,Human_Splice_Rec_473560,Human_Splice_Rec_473588,Human_Splice_Rec_473600,Human_Splice_Rec_473610 Human_miRNA_ID_2038944,Human_miRNA_ID_2617035,Human_miRNA_ID_3017924 RMVar_hsa_circ_42916,RMVar_hsa_circ_63811,RMVar_hsa_circ_70006,RMVar_hsa_circ_351582,RMVar_hsa_circ_220659,RMVar_hsa_circ_301716,RMVar_hsa_circ_220661,RMVar_hsa_circ_322296 99510 RMVar_ID_99510 Human_SNP_ID_151285627 m1A Human chr3 - 122564126 122564126 122564126 CCGGGTCCCAGGGCCAGGCCTCCCTTGTGAGTAGACTATGCAAAGAAAGTAAGTTTCTCCTGTGT CCGGGTCCCAGGGCCAGGCCTCCCTTGTGAGTGGACTATGCAAAGAAAGTAAGTTTCTCCTGTGT T C PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:122564124..122564254 26863196 MeRIP-seq:(Medium) rs1158570472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_473641,Human_Splice_Rec_473683,Human_Splice_Rec_473703,Human_Splice_Rec_473721 99511 RMVar_ID_99511 Human_SNP_ID_151285746 m1A Human chr3 - 122564440 122564440 122564440 ACACCCGCACGAGGAGCGGGGACGGCGGGCGCAGGTGGGAGGCCATGGCTCTGCGCGTCGGGAGG ACACCCGCACGAGGAGCGGGGACGGCGGGCGCCGGTGGGAGGCCATGGCTCTGCGCGTCGGGAGG T G PARP9 Ensembl:ENSG00000138496 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:122564298..122564451 26863196 MeRIP-seq:(Medium) rs759078991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_473621,Human_Splice_Rec_473657 99512 RMVar_ID_99512 Human_SNP_ID_151314737 m1A Human chr3 - 122680879 122680879 122680879 GCAGCGGGAAGGAGCCGGGCACAGCCATCCTCAGCTCCGCTCTCCGCCGGACTGCAGGGGCCGCG GCAGCGGGAAGGAGCCGGGCACAGCCATCCTCGGCTCCGCTCTCCGCCGGACTGCAGGGGCCGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:122680757..122680978 26863196 MeRIP-seq:(Medium) rs1343125526 Functional Loss SNV dbSNP153 33..33 33 - - - 99513 RMVar_ID_99513 Human_SNP_ID_151331128 m1A Human chr3 + 122747864 122747864 122747864 TGGGAAGTGAGGAGCCCCTGTGCCCGGCCGCCACCCCGTCTGGGAGGTGTACCCAACAGCTCATT TGGGAAGTGAGGAGCCCCTGTGCCCGGCCGCCCCCCCGTCTGGGAGGTGTACCCAACAGCTCATT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:122747756..122747960 26863196 MeRIP-seq:(Medium) rs1375495276 Functional Loss SNV dbSNP153 33..33 33 - - - 99514 RMVar_ID_99514 Human_SNP_ID_151332409 m1A Human chr3 + 122753300 122753300 122753300 GGATAAGAGGTACAGGTGAGGGAGGTAGGACTACAGAAGATAGCAAGTAGGTCAGTCTTACTATC GGATAAGAGGTACAGGTGAGGGAGGTAGGACTGCAGAAGATAGCAAGTAGGTCAGTCTTACTATC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:122753215..122753353 26863196 MeRIP-seq:(Medium) rs1277612629 Functional Loss SNV dbSNP153 33..33 33 - - - 99515 RMVar_ID_99515 Human_SNP_ID_151342274 m1A Human chr3 + 122795155 122795155 122795155 ATTCTGCGCTGGGCTAGTCGGCGGTGACCCGGACTGCGCCCGGCAGTGGCTTCGCGGGCGACGCG ATTCTGCGCTGGGCTAGTCGGCGGTGACCCGGCCTGCGCCCGGCAGTGGCTTCGCGGGCGACGCG A C SLC49A4 Ensembl:ENSG00000138463 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:122795112..122795428 26863196 MeRIP-seq:(Medium) rs377194892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756661,Human_RBP_ID_5424829 99516 RMVar_ID_99516 Human_SNP_ID_151342275 m1A Human chr3 + 122795155 122795155 122795155 ATTCTGCGCTGGGCTAGTCGGCGGTGACCCGGACTGCGCCCGGCAGTGGCTTCGCGGGCGACGCG ATTCTGCGCTGGGCTAGTCGGCGGTGACCCGGGCTGCGCCCGGCAGTGGCTTCGCGGGCGACGCG A G SLC49A4 Ensembl:ENSG00000138463 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:122795112..122795428 26863196 MeRIP-seq:(Medium) rs377194892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756661,Human_RBP_ID_5424829 99517 RMVar_ID_99517 Human_SNP_ID_151361140 m1A Human chr3 + 122879444 122879444 122879444 GGAAATCAATACTGCACACTGCACATTTGCTCAGAATTGCACATCTAACAGGAAAAGAGGGAGAA GGAAATCAATACTGCACACTGCACATTTGCTCCGAATTGCACATCTAACAGGAAAAGAGGGAGAA A C SLC49A4 Ensembl:ENSG00000138463 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2288677 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13129,GWAS_ID_13130,GWAS_ID_13131,GWAS_ID_13132,GWAS_ID_13133,GWAS_ID_13134,GWAS_ID_13135 99518 RMVar_ID_99518 Human_SNP_ID_151361141 m1A Human chr3 + 122879444 122879444 122879444 GGAAATCAATACTGCACACTGCACATTTGCTCAGAATTGCACATCTAACAGGAAAAGAGGGAGAA GGAAATCAATACTGCACACTGCACATTTGCTCGGAATTGCACATCTAACAGGAAAAGAGGGAGAA A G SLC49A4 Ensembl:ENSG00000138463 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2288677 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - GWAS_ID_13129,GWAS_ID_13130,GWAS_ID_13131,GWAS_ID_13132,GWAS_ID_13133,GWAS_ID_13134,GWAS_ID_13135 99519 RMVar_ID_99519 Human_SNP_ID_151409931 m1A Human chr3 + 123071955 123071955 123071955 ATGAGGAATGATAGGCCAGGCTGGATGGAGGGAGGGTTTGAGTCTGGGGATGAGGGGAGTAAGAC ATGAGGAATGATAGGCCAGGCTGGATGGAGGGGGGGTTTGAGTCTGGGGATGAGGGGAGTAAGAC A G PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:123071952..123072045 26863196 MeRIP-seq:(Medium) rs1000245816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2744214 RMVar_hsa_circ_220692,RMVar_hsa_circ_94082,RMVar_hsa_circ_97850,RMVar_hsa_circ_220693 99520 RMVar_ID_99520 Human_SNP_ID_151409932 m1A Human chr3 + 123071955 123071955 123071955 ATGAGGAATGATAGGCCAGGCTGGATGGAGGGAGGGTTTGAGTCTGGGGATGAGGGGAGTAAGAC ATGAGGAATGATAGGCCAGGCTGGATGGAGGGTGGGTTTGAGTCTGGGGATGAGGGGAGTAAGAC A T PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:123071952..123072045 26863196 MeRIP-seq:(Medium) rs1000245816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2744214 RMVar_hsa_circ_220692,RMVar_hsa_circ_94082,RMVar_hsa_circ_97850,RMVar_hsa_circ_220693 99521 RMVar_ID_99521 Human_SNP_ID_151413835 m1A Human chr3 + 123089199 123089199 123089199 GGTGGTCCTGCCATCATGGCTGTCCTCTGCAAAGGTCTCCTCGCTCATTGAGAGAATCTCTGACC GGTGGTCCTGCCATCATGGCTGTCCTCTGCAACGGTCTCCTCGCTCATTGAGAGAATCTCTGACC A C PDIA5 Ensembl:ENSG00000065485 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:123089107..123089199 26863196 MeRIP-seq:(Medium) rs762810905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965407,Human_RBP_ID_4756665,Human_RBP_ID_8943495,Human_RBP_ID_9395431,Human_RBP_ID_22456099 Human_Splice_Rec_474414,Human_Splice_Rec_474415,Human_Splice_Rec_474446,Human_Splice_Rec_474447,Human_Splice_Rec_474476,Human_Splice_Rec_474477,Human_Splice_Rec_474485 Human_miRNA_ID_2088632,Human_miRNA_ID_2089510,Human_miRNA_ID_2369243,Human_miRNA_ID_2705523,Human_miRNA_ID_3079393 RMVar_hsa_circ_220694,RMVar_hsa_circ_298790,RMVar_hsa_circ_220692,RMVar_hsa_circ_94082,RMVar_hsa_circ_97850,RMVar_hsa_circ_220693,RMVar_hsa_circ_310700,RMVar_hsa_circ_329735,RMVar_hsa_circ_369588,RMVar_hsa_circ_370581,RMVar_hsa_circ_325719,RMVar_hsa_circ_299053,RMVar_hsa_circ_89601,RMVar_hsa_circ_277516,RMVar_hsa_circ_279850,RMVar_hsa_circ_126757,RMVar_hsa_circ_220698,RMVar_hsa_circ_220700,RMVar_hsa_circ_220701,RMVar_hsa_circ_220702,RMVar_hsa_circ_220699,RMVar_hsa_circ_220696,RMVar_hsa_circ_220697,RMVar_hsa_circ_220695 99522 RMVar_ID_99522 Human_SNP_ID_151426035 m1A Human chr3 + 123140172 123140172 123140172 ATGCTCCAGGTGGGTAGGAAAGAACATGTTCCAGGGCCCTGGGGTAGAAATGAACTTGGTGTGTT ATGCTCCAGGTGGGTAGGAAAGAACATGTTCCGGGGCCCTGGGGTAGAAATGAACTTGGTGTGTT A G PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123139996..123140239 26863196 MeRIP-seq:(Medium) rs561858966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220694,RMVar_hsa_circ_369588,RMVar_hsa_circ_89601,RMVar_hsa_circ_126757,RMVar_hsa_circ_220696,RMVar_hsa_circ_220695,RMVar_hsa_circ_95782,RMVar_hsa_circ_220707,RMVar_hsa_circ_53427,RMVar_hsa_circ_220711,RMVar_hsa_circ_108275,RMVar_hsa_circ_366994,RMVar_hsa_circ_372297,RMVar_hsa_circ_29142,RMVar_hsa_circ_126761,RMVar_hsa_circ_25017,RMVar_hsa_circ_220713,RMVar_hsa_circ_220714,RMVar_hsa_circ_119143,RMVar_hsa_circ_75858,RMVar_hsa_circ_220717,RMVar_hsa_circ_14444,RMVar_hsa_circ_220718 99523 RMVar_ID_99523 Human_SNP_ID_151513276 m1A Human chr3 - 123492131 123492131 123492131 GTTTGCTGAGGTTGGGCTTATTCATTTAACACATACCAACCATTATCCAGAGGCACCATGGAGAG GTTTGCTGAGGTTGGGCTTATTCATTTAACACGTACCAACCATTATCCAGAGGCACCATGGAGAG T C HACD2 Ensembl:ENSG00000206527 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17292764,Human_RBP_ID_22397265 GWAS_ID_13136,GWAS_ID_13137,GWAS_ID_13138 99524 RMVar_ID_99524 Human_SNP_ID_151534832 m1A Human chr3 - 123584996 123584996 123584996 CATGGCGGCAGTGGCGGCGACTGCAGCAGCGAAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGGG CATGGCGGCAGTGGCGGCGACTGCAGCAGCGAGGGGGAATGGGGGCGGCGGTGGCAGGGCCGGGG T C HACD2 Ensembl:ENSG00000206527 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123584402..123585075 26863196 MeRIP-seq:(Medium) rs1405418647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247966,Human_RBP_ID_784249,Human_RBP_ID_4756668,Human_RBP_ID_20971418,Human_RBP_ID_22456103,Human_RBP_ID_24547569 RMVar_hsa_circ_121672,RMVar_hsa_circ_220744,RMVar_hsa_circ_125749,RMVar_hsa_circ_220750 99525 RMVar_ID_99525 Human_SNP_ID_151534833 m1A Human chr3 - 123584996 123584996 123584996 CATGGCGGCAGTGGCGGCGACTGCAGCAGCGAAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGGG CATGGCGGCAGTGGCGGCGACTGCAGCAGCGACGGGGAATGGGGGCGGCGGTGGCAGGGCCGGGG T G HACD2 Ensembl:ENSG00000206527 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123584402..123585075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_247966,Human_RBP_ID_784249,Human_RBP_ID_4756668,Human_RBP_ID_20971418,Human_RBP_ID_22456103,Human_RBP_ID_24547569 RMVar_hsa_circ_121672,RMVar_hsa_circ_220744,RMVar_hsa_circ_125749,RMVar_hsa_circ_220750 99526 RMVar_ID_99526 Human_SNP_ID_151534834 m1A Human chr3 - 123584997 123584997 123584997 ACATGGCGGCAGTGGCGGCGACTGCAGCAGCGAAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGG ACATGGCGGCAGTGGCGGCGACTGCAGCAGCGGAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGG T C HACD2 Ensembl:ENSG00000206527 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:123584514..123585075;chr3:123584425..123585075;chr3:123582226..123585075 26863196 MeRIP-seq:(Medium) rs751944112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247966,Human_RBP_ID_784249,Human_RBP_ID_4756668,Human_RBP_ID_20971418,Human_RBP_ID_22456103,Human_RBP_ID_24547569 RMVar_hsa_circ_121672,RMVar_hsa_circ_220744,RMVar_hsa_circ_125749,RMVar_hsa_circ_220750 99527 RMVar_ID_99527 Human_SNP_ID_151562182 m1A Human chr3 - 123700858 123700858 123700858 TGGCTAGAGGAGGAAGACGGCGAGGACGTGCGAGGGGTGCTGAAGAGGCGCGTGGAGACGAGGCA TGGCTAGAGGAGGAAGACGGCGAGGACGTGCGGGGGGTGCTGAAGAGGCGCGTGGAGACGAGGCA T C MYLK Ensembl:ENSG00000065534 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123700775..123700962 26863196 MeRIP-seq:(Medium) rs1464489033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13186,RMVar_hsa_circ_14221,RMVar_hsa_circ_48095,RMVar_hsa_circ_115667,RMVar_hsa_circ_220754,RMVar_hsa_circ_368568,RMVar_hsa_circ_63037,RMVar_hsa_circ_110116,RMVar_hsa_circ_351638,RMVar_hsa_circ_367674,RMVar_hsa_circ_49592,RMVar_hsa_circ_220757,RMVar_hsa_circ_220758,RMVar_hsa_circ_16015,RMVar_hsa_circ_25528 99528 RMVar_ID_99528 Human_SNP_ID_151562187 m1A Human chr3 + 123700862 123700862 123700862 TCGTCTCCACGCGCCTCTTCAGCACCCCTCGCACGTCCTCGCCGTCTTCCTCCTCTAGCCAACCC TCGTCTCCACGCGCCTCTTCAGCACCCCTCGCGCGTCCTCGCCGTCTTCCTCCTCTAGCCAACCC A G NONHSAG035921.2,NONHSAG035921.2:2 RNACentral:URS00009C0B0F,RNACentral:URS00008C402B lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:123700782..123700956 26863196 MeRIP-seq:(Medium) rs779695227 Functional Loss SNV dbSNP153 33..33 33 - - - 99529 RMVar_ID_99529 Human_SNP_ID_151590266 m1A Human chr3 - 123823778 123823778 123823778 TAATAGGAGATGAGTTTGGGGCAGTGAGCCAGAGCTGGGTGATGCAGGGCCGTGTAGGCCATGGT TAATAGGAGATGAGTTTGGGGCAGTGAGCCAGCGCTGGGTGATGCAGGGCCGTGTAGGCCATGGT T G MYLK Ensembl:ENSG00000065534 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123823737..123823824 26863196 MeRIP-seq:(Medium) rs978274238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35441,RMVar_hsa_circ_302018,RMVar_hsa_circ_290391,RMVar_hsa_circ_220772 99530 RMVar_ID_99530 Human_SNP_ID_151618513 m1A Human chr3 + 123946922 123946922 123946922 TCTGTACATCCTTCACTGTTTTTGTATCTCGCACATGTATGTTTAAATCCTTTCTTTCACTTGTG TCTGTACATCCTTCACTGTTTTTGTATCTCGCGCATGTATGTTTAAATCCTTTCTTTCACTTGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:123946872..123946964 26863196 MeRIP-seq:(Medium) rs568438479 Functional Loss SNV dbSNP153 33..33 33 - - - 99531 RMVar_ID_99531 Human_SNP_ID_151621830 m1A Human chr3 + 123961172 123961172 123961172 TCACCTGGCCCGGTCGAGCTCCAGACCTGACCATCTCTCGCCGCCTCAGAGAAGCCCAGACCGAG TCACCTGGCCCGGTCGAGCTCCAGACCTGACCGTCTCTCGCCGCCTCAGAGAAGCCCAGACCGAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:123961128..123961280 26863196 MeRIP-seq:(Medium) rs1290509244 Functional Loss SNV dbSNP153 33..33 33 - - - 99532 RMVar_ID_99532 Human_SNP_ID_151621857 m1A Human chr3 + 123961213 123961213 123961213 CGCCTCAGAGAAGCCCAGACCGAGGGAAGTGAAGCCTCACGGTAAAAAGAATTAACCGCCGTGGG CGCCTCAGAGAAGCCCAGACCGAGGGAAGTGAGGCCTCACGGTAAAAAGAATTAACCGCCGTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:123961167..123961368 26863196 MeRIP-seq:(Medium) rs771569469 Functional Loss SNV dbSNP153 33..33 33 - - - 99533 RMVar_ID_99533 Human_SNP_ID_151621963 m1A Human chr3 + 123961380 123961380 123961380 CTGCTCCAGGCCCAGCGCCTTGGGCGTACGCAATAGACCCCTCCAAGCTTCCCGGCTTGTCACCC CTGCTCCAGGCCCAGCGCCTTGGGCGTACGCAGTAGACCCCTCCAAGCTTCCCGGCTTGTCACCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:123961277..123961401 26863196 MeRIP-seq:(Medium) rs897968258 Functional Loss SNV dbSNP153 33..33 33 - - - 99534 RMVar_ID_99534 Human_SNP_ID_151798890 m1A Human chr3 - 124730502 124730502 124730502 GAAAGCCTGCACGTCGTACAGACCCGTCACCAATGGCCCCAAAGCTGCACGAGCGACCGCCATTG GAAAGCCTGCACGTCGTACAGACCCGTCACCAGTGGCCCCAAAGCTGCACGAGCGACCGCCATTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:124730451..124730591;chr3:124730451..124730578 26863196 MeRIP-seq:(Medium) rs921007742 Functional Loss SNV dbSNP153 33..33 33 - - - 99535 RMVar_ID_99535 Human_SNP_ID_151825090 m1A Human chr3 - 124829752 124829752 124829752 GGCACATGGAAGGGACCAGAGGAGACAGTGACAATGGAATAAATTCTCCAAAGAGGGTGGGGTTT GGCACATGGAAGGGACCAGAGGAGACAGTGACGATGGAATAAATTCTCCAAAGAGGGTGGGGTTT T C ITGB5 Ensembl:ENSG00000082781 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:124829751..124829889 26863196 MeRIP-seq:(Medium) rs16836078 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13139,GWAS_ID_13140,GWAS_ID_13141,GWAS_ID_13142,GWAS_ID_13143,GWAS_ID_13144 RMVar_hsa_circ_16955,RMVar_hsa_circ_58847,RMVar_hsa_circ_18849,RMVar_hsa_circ_364396,RMVar_hsa_circ_365149,RMVar_hsa_circ_316427,RMVar_hsa_circ_220838,RMVar_hsa_circ_301315,RMVar_hsa_circ_357345,RMVar_hsa_circ_364220,RMVar_hsa_circ_220840,RMVar_hsa_circ_278084,RMVar_hsa_circ_363896,RMVar_hsa_circ_353290,RMVar_hsa_circ_67798,RMVar_hsa_circ_320347,RMVar_hsa_circ_357724,RMVar_hsa_circ_220841,RMVar_hsa_circ_107896,RMVar_hsa_circ_111685,RMVar_hsa_circ_220842 99536 RMVar_ID_99536 Human_SNP_ID_151838572 m1A Human chr3 - 124887289 124887289 124887289 CGGAGCCCAAGTCGCGGCCGCCGAGCGGAGCCAGCCCCTCCCCTACCCGGAGCAGCCCGCTGGGG CGGAGCCCAAGTCGCGGCCGCCGAGCGGAGCCCGCCCCTCCCCTACCCGGAGCAGCCCGCTGGGG T G ITGB5 Ensembl:ENSG00000082781 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:124887194..124887309 26863410 MeRIP-seq:(Medium) rs1559989564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758307,Human_RBP_ID_8729787,Human_RBP_ID_22456108 RMVar_hsa_circ_88801,RMVar_hsa_circ_220845 99537 RMVar_ID_99537 Human_SNP_ID_151838579 m1A Human chr3 + 124887332 124887315 124887332 GGCGGCCGCGACTTGGGCTCCGAGACGCGCCCAGCGCCGAGACTCCCCCGCGCGCCGGCACACTC GGCGGCCGCGACTTGG_________________GCGCCGAGACTCCCCCGCGCGCCGGCACACTC GGCTCCGAGACGCGCCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:124887101..124887668 26863196 MeRIP-seq:(Medium) rs1172282996 Functional Loss DEL dbSNP153 17..33 33 - - - 99538 RMVar_ID_99538 Human_SNP_ID_151838585 m1A Human chr3 + 124887341 124887341 124887341 GACTTGGGCTCCGAGACGCGCCCAGCGCCGAGACTCCCCCGCGCGCCGGCACACTCTGCCCCTGG GACTTGGGCTCCGAGACGCGCCCAGCGCCGAGCCTCCCCCGCGCGCCGGCACACTCTGCCCCTGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:124887024..124887400 26863196 MeRIP-seq:(Medium) rs1248178949 Functional Loss SNV dbSNP153 33..33 33 - - - 99539 RMVar_ID_99539 Human_SNP_ID_151873014 m1A Human chr3 - 125028372 125028372 125028372 TCAGTTGCCCACAAAGGAGAGGAGGAACAGGTAGGACCATTGCGTGAACGGGGTTAGGGACAATC TCAGTTGCCCACAAAGGAGAGGAGGAACAGGTGGGACCATTGCGTGAACGGGGTTAGGGACAATC T C HEG1 Ensembl:ENSG00000173706 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125028370..125028453 26863196 MeRIP-seq:(Medium) rs1439092540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355389,RMVar_hsa_circ_304602,RMVar_hsa_circ_220855,RMVar_hsa_circ_220856,RMVar_hsa_circ_306601 99540 RMVar_ID_99540 Human_SNP_ID_151879467 m1A Human chr3 - 125055634 125055634 125055634 CGCGACCCCCGGCCCCAGCTACAGGGCCCCTGAGCCAGGCGCCGCGACACAGCGGGGACCCTCCG CGCGACCCCCGGCCCCAGCTACAGGGCCCCTGGGCCAGGCGCCGCGACACAGCGGGGACCCTCCG T C HEG1 Ensembl:ENSG00000173706 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:125055449..125055707 26863196 MeRIP-seq:(Medium) rs943673583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_476529 99541 RMVar_ID_99541 Human_SNP_ID_151945567 m1A Human chr3 - 125331233 125331233 125331233 TTAACCTGTATTTGTGTACTTTTGTAGGATAGAGGGAGGAATCAGCAGCTTGGAAATTCAAGCAC TTAACCTGTATTTGTGTACTTTTGTAGGATAGCGGGAGGAATCAGCAGCTTGGAAATTCAAGCAC T G ZNF148 Ensembl:ENSG00000163848 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:125331220..125331291 26863196 MeRIP-seq:(Medium) rs987355525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7114886,Human_RBP_ID_19116032,Human_RBP_ID_22678040 Human_Splice_Rec_476800,Human_Splice_Rec_476801,Human_Splice_Rec_476816,Human_Splice_Rec_476817,Human_Splice_Rec_476826,Human_Splice_Rec_476827,Human_Splice_Rec_476856,Human_Splice_Rec_476857,Human_Splice_Rec_476886,Human_Splice_Rec_476887,Human_Splice_Rec_476892,Human_Splice_Rec_476893,Human_Splice_Rec_476900,Human_Splice_Rec_476901 RMVar_hsa_circ_41287,RMVar_hsa_circ_345170,RMVar_hsa_circ_278305,RMVar_hsa_circ_220872,RMVar_hsa_circ_375576,RMVar_hsa_circ_220873,RMVar_hsa_circ_290761,RMVar_hsa_circ_279728,RMVar_hsa_circ_220881,RMVar_hsa_circ_286676,RMVar_hsa_circ_61337,RMVar_hsa_circ_93452,RMVar_hsa_circ_220884,RMVar_hsa_circ_318685,RMVar_hsa_circ_220885,RMVar_hsa_circ_220888,RMVar_hsa_circ_220890 99542 RMVar_ID_99542 Human_SNP_ID_151952223 m1A Human chr3 - 125358457 125358457 125358457 TAGCTTTGAGGAAATGAGAACAGACAAGAAAAACGCAGTGTTTGAGAAAGTTATTTATGTATTGA TAGCTTTGAGGAAATGAGAACAGACAAGAAAAGCGCAGTGTTTGAGAAAGTTATTTATGTATTGA T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125358454..125358537 26863196 MeRIP-seq:(Medium) rs74532753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10064698,Human_RBP_ID_14599109 RMVar_hsa_circ_220890 99543 RMVar_ID_99543 Human_SNP_ID_151953163 m1A Human chr3 + 125362777 125362777 125362777 AGGTTTCATCATGTTGCCCAGCATGGTCTCGAACTCCTGAGCTCAAGCAATATGCCCACCTCAGC AGGTTTCATCATGTTGCCCAGCATGGTCTCGATCTCCTGAGCTCAAGCAATATGCCCACCTCAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:125362772..125363080 26863196 MeRIP-seq:(Medium) rs1055878978 Functional Loss SNV dbSNP153 33..33 33 - - - 99544 RMVar_ID_99544 Human_SNP_ID_151953314 m1A Human chr3 - 125363552 125363552 125363552 CTCAAAGAAAGAATGGGAAGGTTTGATGGCAGATAGGCTTTTGGGAAACAGTAGAGAAAAAGAAA CTCAAAGAAAGAATGGGAAGGTTTGATGGCAGGTAGGCTTTTGGGAAACAGTAGAGAAAAAGAAA T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125363550..125363633 26863196 MeRIP-seq:(Medium) rs1314991050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14599265 RMVar_hsa_circ_220890 99545 RMVar_ID_99545 Human_SNP_ID_151956213 m1A Human chr3 - 125375082 125375082 125375082 GCGCCCGCCCGCGGTAAAGCGCTCGGCCTGGCAGGCCCGGGCCCGGGGGAGGGCGGGGGAGGGGG GCGCCCGCCCGCGGTAAAGCGCTCGGCCTGGCGGGCCCGGGCCCGGGGGAGGGCGGGGGAGGGGG T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:125375035..125375288 26863196 MeRIP-seq:(Medium) rs1380211455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220890 99546 RMVar_ID_99546 Human_SNP_ID_152009541 m1A Human chr3 - 125594869 125594866 125594870 GGTATCATATTCAGATCAAATCTTAAAAAAAAAAAGTCACCTACAGAACTACAGAATTGTTCTCT GGTATCATATTCAGATCAAATCTTAAAAAAA____GTCACCTACAGAACTACAGAATTGTTCTCT CTTTT C OSBPL11 Ensembl:ENSG00000144909 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125594834..125594995 26863196 MeRIP-seq:(Medium) rs113486299 Functional Loss DEL dbSNP153 32..35 33 - - - 99547 RMVar_ID_99547 Human_SNP_ID_152009683 m1A Human chr3 + 125595298 125595298 125595298 GCAGTTCCCGCCGCAGCCCCCGAGATACAGCCAGGGCCGGCGCGCGCAGCCGGGGAGGAGGGTCG GCAGTTCCCGCCGCAGCCCCCGAGATACAGCCGGGGCCGGCGCGCGCAGCCGGGGAGGAGGGTCG A G lnc-ROPN1B-13 RNACentral:URS00008BDDD0 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr3:125595117..125595560;chr3:125595255..125595573 26863196 MeRIP-seq:(Medium) rs1164836623 Functional Loss SNV dbSNP153 33..33 33 - - - 99548 RMVar_ID_99548 Human_SNP_ID_152009853 m1A Human chr3 - 125595711 125595711 125595711 CGCCCTCCCTCGCCCTCCCTCGCCCATCAGCCAGTCGCCCAGCTACCAGCTCCCAGAGCCTCCGC CGCCCTCCCTCGCCCTCCCTCGCCCATCAGCCGGTCGCCCAGCTACCAGCTCCCAGAGCCTCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:125595662..125595761 26863196 MeRIP-seq:(Medium) rs1244985355 Functional Loss SNV dbSNP153 33..33 33 - - - 99549 RMVar_ID_99549 Human_SNP_ID_152101470 m1A Human chr3 + 125864691 125864691 125864691 TCAGTGCCCCGATCCCTTATTTCTGTGCCCCAACCTCTTATCTCTGTGGCCCGATCCCTTATTTC TCAGTGCCCCGATCCCTTATTTCTGTGCCCCAGCCTCTTATCTCTGTGGCCCGATCCCTTATTTC A G ENPP7P4 Ensembl:ENSG00000241278 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125864623..125864909 26863196 MeRIP-seq:(Medium) rs904577390 Functional Loss SNV dbSNP153 33..33 33 - - - 99550 RMVar_ID_99550 Human_SNP_ID_152102940 m1A Human chr3 - 125868907 125868907 125868907 GAGAGATGAAGCTGAAGGAATATTTTGTGGTAAGGGGTGATATTGTGGGGTTGTTAGAAGAAACA GAGAGATGAAGCTGAAGGAATATTTTGTGGTACGGGGTGATATTGTGGGGTTGTTAGAAGAAACA T G LINC02614 Ensembl:ENSG00000241288 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125868890..125869043 26863196 MeRIP-seq:(Medium) rs1326073772 Functional Loss SNV dbSNP153 33..33 33 - - - 99551 RMVar_ID_99551 Human_SNP_ID_152158443 m1A Human chr3 - 126068215 126068215 126068215 GGGCTGCCAGGCGCCCAGCTGTGCCCAGATGGATGGGACAGAGACCCGGCAGCGGAGGCTGGACA GGGCTGCCAGGCGCCCAGCTGTGCCCAGATGGTTGGGACAGAGACCCGGCAGCGGAGGCTGGACA T A SLC41A3 Ensembl:ENSG00000114544 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:126068113..126068224 26863196 MeRIP-seq:(Medium) rs752939231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588075,Human_RBP_ID_4719977,Human_RBP_ID_22456867,Human_RBP_ID_22508618 Human_Splice_Rec_477250,Human_Splice_Rec_477270,Human_Splice_Rec_477332,Human_Splice_Rec_477382,Human_Splice_Rec_477392,Human_Splice_Rec_477404,Human_Splice_Rec_477418,Human_Splice_Rec_477426,Human_Splice_Rec_477432,Human_Splice_Rec_477438,Human_Splice_Rec_477444,Human_Splice_Rec_477450,Human_Splice_Rec_477456,Human_Splice_Rec_477462,Human_Splice_Rec_477468 Human_miRNA_ID_3062386 RMVar_hsa_circ_81958,RMVar_hsa_circ_220935,RMVar_hsa_circ_353340,RMVar_hsa_circ_363911 99552 RMVar_ID_99552 Human_SNP_ID_152158444 m1A Human chr3 + 126068218 126068218 126068218 CCAGCCTCCGCTGCCGGGTCTCTGTCCCATCCATCTGGGCACAGCTGGGCGCCTGGCAGCCCTAC CCAGCCTCCGCTGCCGGGTCTCTGTCCCATCCGTCTGGGCACAGCTGGGCGCCTGGCAGCCCTAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126068077..126070221 26863196 MeRIP-seq:(Medium) rs1400254614 Functional Loss SNV dbSNP153 33..33 33 - - - 99553 RMVar_ID_99553 Human_SNP_ID_152226877 m1A Human chr3 - 126343183 126343183 126343183 ATGATCACCAGAGGGTGTGGGCAGGTCCCTGGAGCCGGGGGGGGGGGGGGGGGGGGGGGGGGGCA ATGATCACCAGAGGGTGTGGGCAGGTCCCTGGGGCCGGGGGGGGGGGGGGGGGGGGGGGGGGGCA T C KLF15 Ensembl:ENSG00000163884 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr3:126343126..126343281;chr3:126343126..126343278;chr3:126343126..126343200;chr3:126343144..126343261;chr3:126343143..126343245;chr3:126343149..126343281 26863196 MeRIP-seq:(Medium) rs1468297925 Functional Loss SNV dbSNP153 33..33 33 - - - 99554 RMVar_ID_99554 Human_SNP_ID_152226878 m1A Human chr3 + 126343190 126343185 126343190 CCCCCCCCCCCCCCCCCCCCCCGGCTCCAGGGACCTGCCCACACCCTCTGGTGATCATGCTGAGC CCCCCCCCCCCCCCCCCCCCCCGGCTCC_____CCTGCCCACACCCTCTGGTGATCATGCTGAGC CAGGGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:126343152..126343287 26863196 MeRIP-seq:(Medium) rs1157439831 Functional Loss DEL dbSNP153 29..33 33 - - - 99555 RMVar_ID_99555 Human_SNP_ID_152230474 m1A Human chr3 + 126357103 126357103 126357103 CCACCTCCGCGGGGGCCCATCCCGCTCCTCCGACATTCCTCCAGCACTCGCGCGGTGCCTCCGAG CCACCTCCGCGGGGGCCCATCCCGCTCCTCCGGCATTCCTCCAGCACTCGCGCGGTGCCTCCGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:126357092..126357253;chr3:126357083..126357221 26863196 MeRIP-seq:(Medium) rs1340182748 Functional Loss SNV dbSNP153 33..33 33 - - - 99556 RMVar_ID_99556 Human_SNP_ID_152252430 m1A Human chr3 + 126439993 126439993 126439993 AACCTTCTGCTCTCCAGCTCCTCCCCTCAGTCAGCCCAAATACTGATTTCCCTCCTAAGGCACGC AACCTTCTGCTCTCCAGCTCCTCCCCTCAGTCGGCCCAAATACTGATTTCCCTCCTAAGGCACGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126439991..126440077 26863196 MeRIP-seq:(Medium) rs960118902 Functional Loss SNV dbSNP153 33..33 33 - - - 99557 RMVar_ID_99557 Human_SNP_ID_152252641 m1A Human chr3 + 126440879 126440879 126440879 TGAGCCCCAGGCCTGGTCCTGTTTCCTTGGCGAGACTCTCCCAGGACTCTGAACCCACAAACGTG TGAGCCCCAGGCCTGGTCCTGTTTCCTTGGCGCGACTCTCCCAGGACTCTGAACCCACAAACGTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:126440766..126440958 26863196 MeRIP-seq:(Medium) rs1420998984 Functional Loss SNV dbSNP153 33..33 33 - - - 99558 RMVar_ID_99558 Human_SNP_ID_152260273 m1A Human chr3 - 126469654 126469652 126469654 GTTGGAGGCGGAGTGGCCTGGGAGAGCCTCTCAGGGCCAGGAGTGGCAGGCTTGAGTGCTTGGGT GTTGGAGGCGGAGTGGCCTGGGAGAGCCTCTC__GGCCAGGAGTGGCAGGCTTGAGTGCTTGGGT CCT C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126469651..126469746 26863196 MeRIP-seq:(Medium) rs1258188476 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_834674,Human_RBP_ID_17151292 RMVar_hsa_circ_37001,RMVar_hsa_circ_300820,RMVar_hsa_circ_110260,RMVar_hsa_circ_220939,RMVar_hsa_circ_116311,RMVar_hsa_circ_283869,RMVar_hsa_circ_220940,RMVar_hsa_circ_340915 99559 RMVar_ID_99559 Human_SNP_ID_152261919 m1A Human chr3 - 126475270 126475270 126475270 GAAGCACCAGCTCAAGGTGCACCTGCTCACGCACGGCGGCGGTCAGGGCCGGCGGCCCTTCAAGT GAAGCACCAGCTCAAGGTGCACCTGCTCACGCTCGGCGGCGGTCAGGGCCGGCGGCCCTTCAAGT T A ZXDC Ensembl:ENSG00000070476 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:126475222..126475621 32194978 MeRIP-seq:(Medium) rs1399767046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4720224 99560 RMVar_ID_99560 Human_SNP_ID_152262138 m1A Human chr3 - 126475663 126475663 126475663 GGCCTCCGGGCCAAGCCCGCCGCCCGCCGAGGACGACAGCGACGGCGACTCTTTCTTGGTGCTGC GGCCTCCGGGCCAAGCCCGCCGCCCGCCGAGGTCGACAGCGACGGCGACTCTTTCTTGGTGCTGC T A ZXDC Ensembl:ENSG00000070476 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:126475655..126475783 26863196 MeRIP-seq:(Medium) rs775921178 Functional Loss SNV dbSNP153 33..33 33 - - - 99561 RMVar_ID_99561 Human_SNP_ID_152275909 m1A Human chr3 - 126524348 126524348 126524348 CAGACAGGCGGCCGCCAGCACGCGCCGCCGGCAGCAGCGCCTCCCCATGCTGTGCCGGGCGCGCG CAGACAGGCGGCCGCCAGCACGCGCCGCCGGCGGCAGCGCCTCCCCATGCTGTGCCGGGCGCGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126524322..126524392 26863196 MeRIP-seq:(Medium) rs1015735454 Functional Loss SNV dbSNP153 33..33 33 - - - 99562 RMVar_ID_99562 Human_SNP_ID_152279847 m1A Human chr3 + 126539750 126539743 126539750 ACACCCCCCACACCACACACACACCCCACACCACACACTCCACACCACACACACAGCACACACAC ACACCCCCCACACCACACACACACCC_______CACACTCCACACCACACACACAGCACACACAC CCACACCA C CHST13 Ensembl:ENSG00000180767 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126539740..126539942 26863196 MeRIP-seq:(Medium) rs1372402780 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_212921,Human_RBP_ID_26790807 RMVar_hsa_circ_124114,RMVar_hsa_circ_220942 99563 RMVar_ID_99563 Human_SNP_ID_152279854 m1A Human chr3 + 126539750 126539748 126539750 ACACCCCCCACACCACACACACACCCCACACCACACACTCCACACCACACACACAGCACACACAC ACACCCCCCACACCACACACACACCCCACAC__CACACTCCACACCACACACACAGCACACACAC CCA C CHST13 Ensembl:ENSG00000180767 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126539740..126539942 26863196 MeRIP-seq:(Medium) rs752667657 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_212921,Human_RBP_ID_26790807 RMVar_hsa_circ_124114,RMVar_hsa_circ_220942 99564 RMVar_ID_99564 Human_SNP_ID_152284578 m1A Human chr3 + 126556654 126556644 126556654 CTCGCCTCACTGACTGCCGTTCCCACACACACACACACACACACTCACTCTCACAGACACACACA CTCGCCTCACTGACTGCCGTTCC__________CACACACACACTCACTCTCACAGACACACACA CCACACACACA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126556630..126556911 26863196 MeRIP-seq:(Medium) rs35184055 Functional Loss DEL dbSNP153 24..33 33 - - - 99565 RMVar_ID_99565 Human_SNP_ID_152284579 m1A Human chr3 + 126556654 126556644 126556654 CTCGCCTCACTGACTGCCGTTCCCACACACACACACACACACACTCACTCTCACAGACACACACA CTCGCCTCACTGACTGCCGTTCCCA________CACACACACACTCACTCTCACAGACACACACA CCACACACACA CCA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126556630..126556911 26863196 MeRIP-seq:(Medium) rs35184055 Functional Loss DEL dbSNP153 26..33 33 - - - 99566 RMVar_ID_99566 Human_SNP_ID_152284580 m1A Human chr3 + 126556654 126556644 126556654 CTCGCCTCACTGACTGCCGTTCCCACACACACACACACACACACTCACTCTCACAGACACACACA CTCGCCTCACTGACTGCCGTTCCCACA______CACACACACACTCACTCTCACAGACACACACA CCACACACACA CCACA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126556630..126556911 26863196 MeRIP-seq:(Medium) rs35184055 Functional Loss DEL dbSNP153 28..33 33 - - - 99567 RMVar_ID_99567 Human_SNP_ID_152284581 m1A Human chr3 + 126556654 126556644 126556654 CTCGCCTCACTGACTGCCGTTCCCACACACACACACACACACACTCACTCTCACAGACACACACA CTCGCCTCACTGACTGCCGTTCCCACACA____CACACACACACTCACTCTCACAGACACACACA CCACACACACA CCACACA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126556630..126556911 26863196 MeRIP-seq:(Medium) rs35184055 Functional Loss DEL dbSNP153 30..33 33 - - - 99568 RMVar_ID_99568 Human_SNP_ID_152284582 m1A Human chr3 + 126556654 126556644 126556654 CTCGCCTCACTGACTGCCGTTCCCACACACACACACACACACACTCACTCTCACAGACACACACA CTCGCCTCACTGACTGCCGTTCCCACACACA__CACACACACACTCACTCTCACAGACACACACA CCACACACACA CCACACACA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126556630..126556911 26863196 MeRIP-seq:(Medium) rs35184055 Functional Loss DEL dbSNP153 32..33 33 - - - 99569 RMVar_ID_99569 Human_SNP_ID_152307821 m1A Human chr3 + 126654989 126654988 126654990 CCGGCCCGGGCGACTGCGGCGGCGACCGCTCCAGAGTCTCGCTCTCGCTCCTGGCCCGGCCGGGC CCGGCCCGGGCGACTGCGGCGGCGACCGCTCC__AGTCTCGCTCTCGCTCCTGGCCCGGCCGGGC CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:126654939..126655095 26863196 MeRIP-seq:(Medium) rs1267335093 Functional Loss DEL dbSNP153 33..34 33 - - - 99570 RMVar_ID_99570 Human_SNP_ID_152320051 m1A Human chr3 - 126704286 126704286 126704286 CCCCATGGCGAGATGCCGCAGGGCCGGCAGCCACCAGACCCGAGACCCGGCTCCAGAGCAACCGG CCCCATGGCGAGATGCCGCAGGGCCGGCAGCCGCCAGACCCGAGACCCGGCTCCAGAGCAACCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:126704226..126727234;chr3:126704226..126733139 26863196 MeRIP-seq:(Medium) rs1305931020 Functional Loss SNV dbSNP153 33..33 33 - - - 99571 RMVar_ID_99571 Human_SNP_ID_152320053 m1A Human chr3 - 126704290 126704290 126704290 TGCTCCCCATGGCGAGATGCCGCAGGGCCGGCAGCCACCAGACCCGAGACCCGGCTCCAGAGCAA TGCTCCCCATGGCGAGATGCCGCAGGGCCGGCGGCCACCAGACCCGAGACCCGGCTCCAGAGCAA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:126704209..126704336 26863196 MeRIP-seq:(Medium) rs1338937167 Functional Loss SNV dbSNP153 33..33 33 - - - 99572 RMVar_ID_99572 Human_SNP_ID_152320063 m1A Human chr3 - 126704299 126704298 126704299 TGCTCTCCGTGCTCCCCATGGCGAGATGCCGCAGGGCCGGCAGCCACCAGACCCGAGACCCGGCT TGCTCTCCGTGCTCCCCATGGCGAGATGCCGC_GGGCCGGCAGCCACCAGACCCGAGACCCGGCT CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:126704226..126852774;chr3:126704251..126727145 26863196 MeRIP-seq:(Medium) rs745802050 Functional Loss DEL dbSNP153 33..33 33 - - - 99573 RMVar_ID_99573 Human_SNP_ID_152325447 m1A Human chr3 - 126727131 126727130 126727131 CCATCTTGAAGGCCAAAGGTAGAAGATGTGGGAGCAGGGGGTGGAGAGCTGGGCTCCTTCATGCG CCATCTTGAAGGCCAAAGGTAGAAGATGTGGG_GCAGGGGGTGGAGAGCTGGGCTCCTTCATGCG CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:126704318..126949266 32194978 MeRIP-seq:(Medium) rs762989438 Functional Loss DEL dbSNP153 33..33 33 - - - 99574 RMVar_ID_99574 Human_SNP_ID_152325449 m1A Human chr3 - 126727131 126727131 126727131 CCATCTTGAAGGCCAAAGGTAGAAGATGTGGGAGCAGGGGGTGGAGAGCTGGGCTCCTTCATGCG CCATCTTGAAGGCCAAAGGTAGAAGATGTGGGGGCAGGGGGTGGAGAGCTGGGCTCCTTCATGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:126704318..126949266 32194978 MeRIP-seq:(Medium) rs1001157312 Functional Loss SNV dbSNP153 33..33 33 - - - 99575 RMVar_ID_99575 Human_SNP_ID_152326918 m1A Human chr3 + 126733165 126733165 126733165 GAAAGAGAGGCTGCCACCAAGCACTCCAAGGCATCCCTGCCCACGGGCGAAGGCAGCATCAGCCA GAAAGAGAGGCTGCCACCAAGCACTCCAAGGCGTCCCTGCCCACGGGCGAAGGCAGCATCAGCCA A G CHCHD6 Ensembl:ENSG00000159685 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:126733030..126733267 26863196 MeRIP-seq:(Medium) rs1227545633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588245,Human_RBP_ID_19012924 Human_Splice_Rec_478282,Human_Splice_Rec_478283,Human_Splice_Rec_478296,Human_Splice_Rec_478297,Human_Splice_Rec_478310,Human_Splice_Rec_478311,Human_Splice_Rec_478322,Human_Splice_Rec_478323,Human_Splice_Rec_478330,Human_Splice_Rec_478331 Human_miRNA_ID_2869424 RMVar_hsa_circ_2227,RMVar_hsa_circ_278230,RMVar_hsa_circ_310674,RMVar_hsa_circ_79602,RMVar_hsa_circ_220956,RMVar_hsa_circ_122690,RMVar_hsa_circ_220953,RMVar_hsa_circ_220954,RMVar_hsa_circ_86628,RMVar_hsa_circ_220955 99576 RMVar_ID_99576 Human_SNP_ID_152336028 m1A Human chr3 + 126772384 126772384 126772384 CCTCCCAAAGTGCTGGAATTACAGGCGTGATCATAGGTCTTTAAGAACTTCCCTTATGAACCTGG CCTCCCAAAGTGCTGGAATTACAGGCGTGATCGTAGGTCTTTAAGAACTTCCCTTATGAACCTGG A G CHCHD6 Ensembl:ENSG00000159685 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:126772371..126772498 26863196 MeRIP-seq:(Medium) rs557112001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14604843 RMVar_hsa_circ_2227,RMVar_hsa_circ_310674,RMVar_hsa_circ_79602,RMVar_hsa_circ_220956,RMVar_hsa_circ_220953,RMVar_hsa_circ_86628 99577 RMVar_ID_99577 Human_SNP_ID_152359856 m1A Human chr3 + 126865500 126865500 126865500 CTTTCATCAACTCCATCACCAACTTCGCCTTCACCACCACCACCATCTCCACCATCCTCCATAAC CTTTCATCAACTCCATCACCAACTTCGCCTTCCCCACCACCACCATCTCCACCATCCTCCATAAC A C CHCHD6 Ensembl:ENSG00000159685 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:126865494..126865598 26863196 MeRIP-seq:(Medium) rs1163942535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79602,RMVar_hsa_circ_220956,RMVar_hsa_circ_220953,RMVar_hsa_circ_86628 99578 RMVar_ID_99578 Human_SNP_ID_152378435 m1A Human chr3 - 126944954 126944954 126944954 CAAACAATGAAACCTCTGCCCTGCCCTCAGGGACCCCTCTCACCCACCCACAGCCACAAGGCCTA CAAACAATGAAACCTCTGCCCTGCCCTCAGGGGCCCCTCTCACCCACCCACAGCCACAAGGCCTA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:126944949..126945151 26863196 MeRIP-seq:(Medium) rs1292885061 Functional Loss SNV dbSNP153 33..33 33 - - - 99579 RMVar_ID_99579 Human_SNP_ID_152379705 m1A Human chr3 + 126949705 126949705 126949705 GGACGGAAGGGAAGGCTGTACAGAGCCTTATCACCAATGGGAAGGAAAGGCTGCACGGAGGCTTG GGACGGAAGGGAAGGCTGTACAGAGCCTTATCGCCAATGGGAAGGAAAGGCTGCACGGAGGCTTG A G CHCHD6 Ensembl:ENSG00000159685 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:126949670..126949824 26863196 MeRIP-seq:(Medium) rs1424552086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79602,RMVar_hsa_circ_220956,RMVar_hsa_circ_220953,RMVar_hsa_circ_86628 99580 RMVar_ID_99580 Human_SNP_ID_152381580 m1A Human chr3 - 126957499 126957499 126957499 AGCGCTGGTATGCCTTGACCAGGTCCGAGCACAGCAGCACCTCATGCGGGCGATCTCGGTAGCAG AGCGCTGGTATGCCTTGACCAGGTCCGAGCACGGCAGCACCTCATGCGGGCGATCTCGGTAGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:126957320..126957601 32194978 MeRIP-seq:(Medium) rs775923561 Functional Loss SNV dbSNP153 33..33 33 - - - 99581 RMVar_ID_99581 Human_SNP_ID_152382321 m1A Human chr3 + 126960310 126960310 126960310 GTGCCCTGCCGTTTCCTGCTGGGCCCCTGCATATGCCCCTGAGCCTGGGGCTGCCACGTGTTTAG GTGCCCTGCCGTTTCCTGCTGGGCCCCTGCATGTGCCCCTGAGCCTGGGGCTGCCACGTGTTTAG A G CHCHD6 Ensembl:ENSG00000159685 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126960260..126960331 26863196 MeRIP-seq:(Medium) rs1032705691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588267,Human_RBP_ID_4760375,Human_RBP_ID_17661188,Human_RBP_ID_22768936,Human_RBP_ID_26824057 Human_miRNA_ID_2268671 RMVar_hsa_circ_79602,RMVar_hsa_circ_220956,RMVar_hsa_circ_220953,RMVar_hsa_circ_86628 99582 RMVar_ID_99582 Human_SNP_ID_152389628 m1A Human chr3 - 126988764 126988764 126988764 ACTGCGCCCACATACACCTCGCCTGTCTGCTCATGCACCACTAGGTGGGTGAGGCCCCAGTCGCT ACTGCGCCCACATACACCTCGCCTGTCTGCTCGTGCACCACTAGGTGGGTGAGGCCCCAGTCGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:126988714..126988784 26863196 MeRIP-seq:(Medium) rs918027854 Functional Loss SNV dbSNP153 33..33 33 - - - 99583 RMVar_ID_99583 Human_SNP_ID_152435461 m1A Human chr3 - 127154965 127154964 127154965 ACTCAGACACATACACACACAGACACACAGACACACAAACACACACACTCACAGACACACAGACA ACTCAGACACATACACACACAGACACACAGAC_CACAAACACACACACTCACAGACACACAGACA GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:127154927..127155079 26863196 MeRIP-seq:(Medium) rs1559994857 Functional Loss DEL dbSNP153 33..33 33 - - - 99584 RMVar_ID_99584 Human_SNP_ID_152541105 m1A Human chr3 + 127575553 127575553 127575553 GGTGGGTCGTGAGGTCCCACCCTGGACAGGCCAGGCTCTGCCTCCAGCACCTACTACCCTCAAGC GGTGGGTCGTGAGGTCCCACCCTGGACAGGCCGGGCTCTGCCTCCAGCACCTACTACCCTCAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:127575527..127575707 26863196 MeRIP-seq:(Medium) rs1280747992 Functional Loss SNV dbSNP153 33..33 33 - - - 99585 RMVar_ID_99585 Human_SNP_ID_152542338 m1A Human chr3 + 127580072 127580072 127580072 TCGTAGAGCAGCAGCAGGCAGCGATGAGGCACACTGATGTTTGGTGCCAGGGGTGGGGGTAGCGC TCGTAGAGCAGCAGCAGGCAGCGATGAGGCACGCTGATGTTTGGTGCCAGGGGTGGGGGTAGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:127579996..127580078 26863196 MeRIP-seq:(Medium) rs1193574161 Functional Loss SNV dbSNP153 33..33 33 - - - 99586 RMVar_ID_99586 Human_SNP_ID_152545140 m1A Human chr3 - 127590696 127590696 127590696 TGTGGCCGTTTTCGCAATTTGGGCTGGACGAAAAAGACGGTCTTGCTTTCCCGGTCGCCGCTGTC TGTGGCCGTTTTCGCAATTTGGGCTGGACGAAGAAGACGGTCTTGCTTTCCCGGTCGCCGCTGTC T C TPRA1 Ensembl:ENSG00000163870 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:127590576..127590725 26863196 MeRIP-seq:(Medium) rs1257928901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588364,Human_RBP_ID_5531012 RMVar_hsa_circ_33754,RMVar_hsa_circ_82816,RMVar_hsa_circ_220991,RMVar_hsa_circ_86441,RMVar_hsa_circ_220994 99587 RMVar_ID_99587 Human_SNP_ID_152547040 m1A Human chr3 - 127598468 127598468 127598468 CCCGCCCGCCACGCGCCAGCGCGCTCACCGCCATAGCAGTACCACGATCCTCTCCGCCACTACAG CCCGCCCGCCACGCGCCAGCGCGCTCACCGCCGTAGCAGTACCACGATCCTCTCCGCCACTACAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:127598401..127598530;chr3:127598401..127598547 26863196 MeRIP-seq:(Medium) rs1174315265 Functional Loss SNV dbSNP153 33..33 33 - - - 99588 RMVar_ID_99588 Human_SNP_ID_152547389 m1A Human chr3 - 127599526 127599523 127599527 AATGAAATTACCTTTCCATGCCATCTCCAATGAGCTCCTCTCCATCCTCTTCTTCCTCCAGGGGC AATGAAATTACCTTTCCATGCCATCTCCAAT____TCCTCTCCATCCTCTTCTTCCTCCAGGGGC AGCTC A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:127599501..127599525 32194978 MeRIP-seq:(Medium) rs1294696364 Functional Loss DEL dbSNP153 32..35 33 - - - 99589 RMVar_ID_99589 Human_SNP_ID_152548769 m1A Human chr3 + 127604962 127604962 127604962 CAAGCGCCGCCAGGTGGAGCGGGCCACGGAGGACGGCGAGGAGGACGAGGAGATGATCGAGAGCA CAAGCGCCGCCAGGTGGAGCGGGCCACGGAGGGCGGCGAGGAGGACGAGGAGATGATCGAGAGCA A G MCM2 Ensembl:ENSG00000073111 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:127604601..127606200 26863196 MeRIP-seq:(Medium) rs747807511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4720909,Human_RBP_ID_5205912,Human_RBP_ID_8875130,Human_RBP_ID_23026759 Human_Splice_Rec_479078,Human_Splice_Rec_479108,Human_Splice_Rec_479142,Human_Splice_Rec_479168 RMVar_hsa_circ_52356,RMVar_hsa_circ_120433,RMVar_hsa_circ_52677,RMVar_hsa_circ_97888,RMVar_hsa_circ_220995,RMVar_hsa_circ_220996,RMVar_hsa_circ_105151,RMVar_hsa_circ_40863,RMVar_hsa_circ_101595,RMVar_hsa_circ_220997,RMVar_hsa_circ_41570,RMVar_hsa_circ_220998 99590 RMVar_ID_99590 Human_SNP_ID_152549148 m1A Human chr3 - 127606080 127606080 127606080 AGGGGGCACAGTGGGAAGAGAGTTAACTAAGCATGAGGCCTGGGCTGGGCTGCAACAATGCCTGT AGGGGGCACAGTGGGAAGAGAGTTAACTAAGCGTGAGGCCTGGGCTGGGCTGCAACAATGCCTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:127606079..127606205 26863196 MeRIP-seq:(Medium) rs773844935 Functional Loss SNV dbSNP153 33..33 33 - - - 99591 RMVar_ID_99591 Human_SNP_ID_152549437 m1A Human chr3 - 127606819 127606819 127606819 GACAGCTGGCAGCAGACCTTGTGTCCTCTCTCACCTCCTCCATGTTGACCTCAAAGGGGCCGGCC GACAGCTGGCAGCAGACCTTGTGTCCTCTCTCGCCTCCTCCATGTTGACCTCAAAGGGGCCGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:127606776..127606825 32194978 MeRIP-seq:(Medium) rs1342667713 Functional Loss SNV dbSNP153 33..33 33 - - - 99592 RMVar_ID_99592 Human_SNP_ID_152555204 m1A Human chr3 - 127629262 127629250 127629262 CTCACCCCCAACCAGCAGAAGCAGCAGCGGCGAAAGCAGCGGCGGCAGCCGGGCGGCCCGCAGCA CTCACCCCCAACCAGCAGAAGCAGCAGCGGCG____________GCAGCCGGGCGGCCCGCAGCA CCGCCGCTGCTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:127629213..127629300 26863196 MeRIP-seq:(Medium) rs1166605606 Functional Loss DEL dbSNP153 33..44 33 - - - 99593 RMVar_ID_99593 Human_SNP_ID_152555213 m1A Human chr3 - 127629269 127629269 127629269 GAGCGCACTCACCCCCAACCAGCAGAAGCAGCAGCGGCGAAAGCAGCGGCGGCAGCCGGGCGGCC GAGCGCACTCACCCCCAACCAGCAGAAGCAGCGGCGGCGAAAGCAGCGGCGGCAGCCGGGCGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:127629220..127629346 26863196 MeRIP-seq:(Medium) rs1212278376 Functional Loss SNV dbSNP153 33..33 33 - - - 99594 RMVar_ID_99594 Human_SNP_ID_152557463 m1A Human chr3 + 127639293 127639293 127639293 CTGTGTGGCTGGGTCTGATGAGCCTGGCCCAGAGGGCCTCACCTCCACCTCCCTGCTAGACCTCC CTGTGTGGCTGGGTCTGATGAGCCTGGCCCAGGGGGCCTCACCTCCACCTCCCTGCTAGACCTCC A G PODXL2 Ensembl:ENSG00000114631 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:127639219..127639351 26863196 MeRIP-seq:(Medium) rs1278836159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1309587,Human_RBP_ID_4756704,Human_RBP_ID_8557743,Human_RBP_ID_17993371 Human_Splice_Rec_479212 Human_miRNA_ID_937051,Human_miRNA_ID_1366939 RMVar_hsa_circ_221004,RMVar_hsa_circ_343531,RMVar_hsa_circ_362747,RMVar_hsa_circ_287194 99595 RMVar_ID_99595 Human_SNP_ID_152562457 m1A Human chr3 + 127660571 127660569 127660572 GAGGAGAGGGAGAAGGAAGAGGTAGAGAAACAAGAGGAGGAGGAAGAGGAGGAGCTGCTCCCTGT GAGGAGAGGGAGAAGGAAGAGGTAGAGAAAC___AGGAGGAGGAAGAGGAGGAGCTGCTCCCTGT CAAG C PODXL2 Ensembl:ENSG00000114631 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:127660451..127661006 26863196 MeRIP-seq:(Medium) rs1189624326 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_212419,Human_RBP_ID_7117172 RMVar_hsa_circ_221004,RMVar_hsa_circ_343531,RMVar_hsa_circ_287194,RMVar_hsa_circ_221005,RMVar_hsa_circ_322571 99596 RMVar_ID_99596 Human_SNP_ID_152565578 m1A Human chr3 + 127672513 127672513 127672513 GCGCAGCCGAGGCGCAGGCCGAGTGGGCCGCCAGGACCAAGCGAGGTGGACCCCGAAACGGACGG GCGCAGCCGAGGCGCAGGCCGAGTGGGCCGCCTGGACCAAGCGAGGTGGACCCCGAAACGGACGG A T PODXL2 Ensembl:ENSG00000114631 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:127672367..127672725 26863196 MeRIP-seq:(Medium) rs914242068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588425,Human_RBP_ID_17661189 99597 RMVar_ID_99597 Human_SNP_ID_152565628 m1A Human chr3 - 127672611 127672611 127672611 GCCGCCGTGTGAAGTCGGGGGAAGCGGGAAGGAGCCCGCGCCGAGGGCCAGGCCGCGGGGGCGGC GCCGCCGTGTGAAGTCGGGGGAAGCGGGAAGGCGCCCGCGCCGAGGGCCAGGCCGCGGGGGCGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:127672311..127672775 26863410 MeRIP-seq:(Medium) rs1239006962 Functional Loss SNV dbSNP153 33..33 33 - - - 99598 RMVar_ID_99598 Human_SNP_ID_152581468 m1A Human chr3 + 127730355 127730355 127730355 ATGCAGCCTGCACATCCCAGCCCAGTATTCCCAGCCTCCCAGGAAGGCTTCTACTTGTTCCTCTG ATGCAGCCTGCACATCCCAGCCCAGTATTCCCCGCCTCCCAGGAAGGCTTCTACTTGTTCCTCTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:127730348..127730502 26863196 MeRIP-seq:(Medium) rs933256351 Functional Loss SNV dbSNP153 33..33 33 - - - 99599 RMVar_ID_99599 Human_SNP_ID_152585449 m1A Human chr3 + 127746660 127746660 127746660 CTGTCTTTGTGGGGGTAGAACTGCAGGTTCACATTCCACTCTTCCGTCTCCCTCTGCGTCCACTC CTGTCTTTGTGGGGGTAGAACTGCAGGTTCACGTTCCACTCTTCCGTCTCCCTCTGCGTCCACTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:127746657..127746830 26863196 MeRIP-seq:(Medium) rs1003166884 Functional Loss SNV dbSNP153 33..33 33 - - - 99600 RMVar_ID_99600 Human_SNP_ID_152603343 m1A Human chr3 + 127822423 127822423 127822423 TCATCTGGGCGGCCCCAAGGCAGCAGGAAGGCAGCTCCGAGCCCTCTTCCCGCACCCAGACCCTG TCATCTGGGCGGCCCCAAGGCAGCAGGAAGGCGGCTCCGAGCCCTCTTCCCGCACCCAGACCCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:127822420..127822513 26863196 MeRIP-seq:(Medium) rs890094816 Functional Loss SNV dbSNP153 33..33 33 - - - 99601 RMVar_ID_99601 Human_SNP_ID_152603588 m1A Human chr3 + 127823155 127823155 127823155 CGGATCCTCGTTTGCGGCGGGCCAGGGCCGGGACGAGCTGCGCGCGACCGGCTTCGCGGCGACAG CGGATCCTCGTTTGCGGCGGGCCAGGGCCGGGGCGAGCTGCGCGCGACCGGCTTCGCGGCGACAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:127823105..127823287 26863196 MeRIP-seq:(Medium) rs967821294 Functional Loss SNV dbSNP153 33..33 33 - - - 99602 RMVar_ID_99602 Human_SNP_ID_152656147 m1A Human chr3 + 128052789 128052789 128052789 GCAGAAGGCGTCCCTGGGTAGCGCGGAAGGTTACTTCTCTGTGTCCCAACTCTTCCTGTTTTGTT GCAGAAGGCGTCCCTGGGTAGCGCGGAAGGTTGCTTCTCTGTGTCCCAACTCTTCCTGTTTTGTT A G SEC61A1 Ensembl:ENSG00000058262 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128052786..128052900 26863196 MeRIP-seq:(Medium) rs781084823 Functional Loss SNV dbSNP153 33..33 33 - - - 99603 RMVar_ID_99603 Human_SNP_ID_152659682 m1A Human chr3 - 128067101 128067101 128067101 GCTGACCAGCAAGTTGCCACTGAAGCGAGCTGAGAGCATTTGGGAGATGACATAAAGGTTGGACA GCTGACCAGCAAGTTGCCACTGAAGCGAGCTGGGAGCATTTGGGAGATGACATAAAGGTTGGACA T C RUVBL1 Ensembl:ENSG00000175792 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:128067051..128067100 26863196 MeRIP-seq:(Medium) rs779751114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221024,RMVar_hsa_circ_221023,RMVar_hsa_circ_84988,RMVar_hsa_circ_221033 99604 RMVar_ID_99604 Human_SNP_ID_152660518 m1A Human chr3 - 128070352 128070352 128070352 GACCCAAGTGGACTAAACACGGAGCTAGCAGAAACAGGCAGACTCTAAGCCCAACCAGAAGAGTC GACCCAAGTGGACTAAACACGGAGCTAGCAGACACAGGCAGACTCTAAGCCCAACCAGAAGAGTC T G RUVBL1 Ensembl:ENSG00000175792 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128070301..128070634 32194978 MeRIP-seq:(Medium) rs1351513190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18796164 RMVar_hsa_circ_22170,RMVar_hsa_circ_221024,RMVar_hsa_circ_221023,RMVar_hsa_circ_84988,RMVar_hsa_circ_221033 99605 RMVar_ID_99605 Human_SNP_ID_152663210 m1A Human chr3 + 128081130 128081130 128081130 TTAAAAAGAAATGCTTTCCACACTGAACTGACAGCGCTGCAGACCACGCCTGAGTGGGGACGGCA TTAAAAAGAAATGCTTTCCACACTGAACTGACGGCGCTGCAGACCACGCCTGAGTGGGGACGGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128081083..128081183 32194978 MeRIP-seq:(Medium) rs1410519195 Functional Loss SNV dbSNP153 33..33 33 - - - 99606 RMVar_ID_99606 Human_SNP_ID_152672800 m1A Human chr3 - 128123705 128123705 128123705 CGGCGTCTGCAAAATGAAGATTGAGGAGGTGAAGAGCACTACGAAGACGCAGCGCATCGCCTCCC CGGCGTCTGCAAAATGAAGATTGAGGAGGTGAGGAGCACTACGAAGACGCAGCGCATCGCCTCCC T C RUVBL1 Ensembl:ENSG00000175792 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128123531..128153864 26863196 MeRIP-seq:(Medium) rs780954599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933303,Human_RBP_ID_1617199,Human_RBP_ID_1948651,Human_RBP_ID_3685242,Human_RBP_ID_4757419,Human_RBP_ID_5325306,Human_RBP_ID_5474813,Human_RBP_ID_7117622,Human_RBP_ID_8557901,Human_RBP_ID_8875145,Human_RBP_ID_9394054,Human_RBP_ID_14609141,Human_RBP_ID_18445946,Human_RBP_ID_18796221,Human_RBP_ID_23967363,Human_RBP_ID_26347178 RMVar_hsa_circ_83677,RMVar_hsa_circ_221047 99607 RMVar_ID_99607 Human_SNP_ID_152672824 m1A Human chr3 + 128123759 128123759 128123759 TGCAGACGCCGGGAGCTAAAACCAGCGTGGAAAACCAGCAGCTAGGACAGTGCGCCCGGCGCCTG TGCAGACGCCGGGAGCTAAAACCAGCGTGGAACACCAGCAGCTAGGACAGTGCGCCCGGCGCCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128123492..128123825 26863196 MeRIP-seq:(Medium) rs776981572 Functional Loss SNV dbSNP153 33..33 33 - - - 99608 RMVar_ID_99608 Human_SNP_ID_152680381 m1A Human chr3 + 128153526 128153526 128153526 GCGGCGGCGGCGGCATGGCAGGGCGGCGGGTGAACGTGAACGTGGGCGTGCTGGGCCACATCGAC GCGGCGGCGGCGGCATGGCAGGGCGGCGGGTGGACGTGAACGTGGGCGTGCTGGGCCACATCGAC A G EEFSEC Ensembl:ENSG00000132394 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:128153453..128246861 26863196 MeRIP-seq:(Medium) rs1455763781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424301 RMVar_hsa_circ_99724,RMVar_hsa_circ_221049 99609 RMVar_ID_99609 Human_SNP_ID_152702721 m1A Human chr3 + 128255276 128255276 128255276 TGATGAAGAAGGGCCTCTCGGGGACGTGAAGGATAGTCAAGGGCCATGGAAATAAAGGTATGGGG TGATGAAGAAGGGCCTCTCGGGGACGTGAAGGGTAGTCAAGGGCCATGGAAATAAAGGTATGGGG A G EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128255236..128255414 26863196 MeRIP-seq:(Medium) rs983196914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99724,RMVar_hsa_circ_221049,RMVar_hsa_circ_31713,RMVar_hsa_circ_276158,RMVar_hsa_circ_221052,RMVar_hsa_circ_27769 99610 RMVar_ID_99610 Human_SNP_ID_152720292 m1A Human chr3 + 128335395 128335395 128335395 TGGGTGGGGTGACTGAGGAGGGGCTCTGATACAGTGGCATCCAAGCAGGTATGGGAAGGAAGTGA TGGGTGGGGTGACTGAGGAGGGGCTCTGATACGGTGGCATCCAAGCAGGTATGGGAAGGAAGTGA A G EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128335385..128335568 26863196 MeRIP-seq:(Medium) rs967741392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7796,RMVar_hsa_circ_99724,RMVar_hsa_circ_221049,RMVar_hsa_circ_31713,RMVar_hsa_circ_27769,RMVar_hsa_circ_375824,RMVar_hsa_circ_18754,RMVar_hsa_circ_221054,RMVar_hsa_circ_52660 99611 RMVar_ID_99611 Human_SNP_ID_152725790 m1A Human chr3 + 128359144 128359144 128359144 TTGCTGAGCATGCTGCTTTGGATAGGGTGATCAGGGAAGGACAGAGGGAGGGAAGGAGCCACATG TTGCTGAGCATGCTGCTTTGGATAGGGTGATCGGGGAAGGACAGAGGGAGGGAAGGAGCCACATG A G EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128359140..128359284 26863196 MeRIP-seq:(Medium) rs1239257958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99724,RMVar_hsa_circ_221049 99612 RMVar_ID_99612 Human_SNP_ID_152737097 m1A Human chr3 + 128408206 128408206 128408206 GCGAGCCCTCACAGCATGTGGTGCTCAGCCTGACTTTCAAGCGTTATGTCTTCGACACCCACAAG GCGAGCCCTCACAGCATGTGGTGCTCAGCCTGCCTTTCAAGCGTTATGTCTTCGACACCCACAAG A C EEFSEC Ensembl:ENSG00000132394 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128408156..128408392 26863196 MeRIP-seq:(Medium) rs1430515876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99724,RMVar_hsa_circ_221049 99613 RMVar_ID_99613 Human_SNP_ID_152756217 m1A Human chr3 - 128480517 128480517 128480517 CACCCTCTTCTCCTCTGGCTTCCCTCTCTGAAATAGCCGAACTCCAGGCTGGGCTGAGCCAAAGC CACCCTCTTCTCCTCTGGCTTCCCTCTCTGAAGTAGCCGAACTCCAGGCTGGGCTGAGCCAAAGC T C GATA2 Ensembl:ENSG00000179348 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:128480466..128480814 32194978 MeRIP-seq:(Medium) rs1019858401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510540,Human_RBP_ID_27497788 99614 RMVar_ID_99614 Human_SNP_ID_152756383 m1A Human chr3 + 128481068 128481068 128481068 CCATGCTGGACGGGTGGGGGTGGCCGAAGGAGAGGCTGGAGGAGGGGTGGATGGGCGTCGGAGTG CCATGCTGGACGGGTGGGGGTGGCCGAAGGAGGGGCTGGAGGAGGGGTGGATGGGCGTCGGAGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128481018..128481181 26863196 MeRIP-seq:(Medium) rs1559984558 Functional Loss SNV dbSNP153 33..33 33 - - - 99615 RMVar_ID_99615 Human_SNP_ID_152756694 m1A Human chr3 + 128481909 128481909 128481909 CGGCGCCATAAGGTGGTGGTTGTCGTCTGACAATTTGCACAACAGGTGCCGGCTCTTCTGGCGGC CGGCGCCATAAGGTGGTGGTTGTCGTCTGACAGTTTGCACAACAGGTGCCGGCTCTTCTGGCGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:128481858..128481958 32194978 MeRIP-seq:(Medium) rs544866789 Functional Loss SNV dbSNP153 33..33 33 - - - 99616 RMVar_ID_99616 Human_SNP_ID_152757871 m1A Human chr3 - 128485874 128485874 128485874 CAGGCCTAGCTACTATGGGCACCCAGCCTGCTACACACCACCCCATCCCCACCTACCCCTCCTAT CAGGCCTAGCTACTATGGGCACCCAGCCTGCTGCACACCACCCCATCCCCACCTACCCCTCCTAT T C GATA2 Ensembl:ENSG00000179348 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128485823..128485940 26863196 MeRIP-seq:(Medium) rs886057931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27497809 Clinvar_Rec_611 RMVar_hsa_circ_51147 99617 RMVar_ID_99617 Human_SNP_ID_152758347 m1A Human chr3 - 128487001 128487001 128487001 CCATGGAGGTGGCGCCCGAGCAGCCGCGCTGGATGGCGCACCCGGCCGTGCTGAATGCGCAGCAC CCATGGAGGTGGCGCCCGAGCAGCCGCGCTGGGTGGCGCACCCGGCCGTGCTGAATGCGCAGCAC T C GATA2 Ensembl:ENSG00000179348 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:128486951..128487897 26863196 MeRIP-seq:(Medium) rs774005466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_479782,Human_Splice_Rec_479794,Human_Splice_Rec_479806,Human_Splice_Rec_479816,Human_Splice_Rec_479822 RMVar_hsa_circ_51147 99618 RMVar_ID_99618 Human_SNP_ID_152758361 m1A Human chr3 + 128487024 128487024 128487024 GGTGCGCCATCCAGCGCGGCTGCTCGGGCGCCACCTCCATGGCCGGCGGCGGCGGCTCAGGGTCT GGTGCGCCATCCAGCGCGGCTGCTCGGGCGCCGCCTCCATGGCCGGCGGCGGCGGCTCAGGGTCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:128486939..128487024 26863410 MeRIP-seq:(Medium) rs1220018679 Functional Loss SNV dbSNP153 33..33 33 - - - 99619 RMVar_ID_99619 Human_SNP_ID_152758562 m1A Human chr3 + 128487770 128487770 128487770 TCGGCCTCTGAGAGTGAAGGAGTTCCGGCGGGAGCCCCGAGGGCGACGGGCCCAGGGACAGCACG TCGGCCTCTGAGAGTGAAGGAGTTCCGGCGGGCGCCCCGAGGGCGACGGGCCCAGGGACAGCACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:128486983..128487900;chr3:128487673..128487906 26863196 MeRIP-seq:(Medium) rs1247951998 Functional Loss SNV dbSNP153 33..33 33 - - - 99620 RMVar_ID_99620 Human_SNP_ID_152758567 m1A Human chr3 + 128487777 128487777 128487777 CTGAGAGTGAAGGAGTTCCGGCGGGAGCCCCGAGGGCGACGGGCCCAGGGACAGCACGTCCGGAG CTGAGAGTGAAGGAGTTCCGGCGGGAGCCCCGCGGGCGACGGGCCCAGGGACAGCACGTCCGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128487685..128487911 26863196 MeRIP-seq:(Medium) rs1347970031 Functional Loss SNV dbSNP153 33..33 33 - - - 99621 RMVar_ID_99621 Human_SNP_ID_152758709 m1A Human chr3 + 128488130 128488130 128488130 GCTCCTGGCGGCCCCTGCTGCCAACGCGCCCCACCACTAAGGGACCCTCACCCCAAGGCCCGACC GCTCCTGGCGGCCCCTGCTGCCAACGCGCCCCGCCACTAAGGGACCCTCACCCCAAGGCCCGACC A G GATA2-AS1,GATA2-AS1:2,GATA2-AS1:3,GATA2-AS1:4 RNACentral:URS0000D590D0,RNACentral:URS0000D57DED,RNACentral:URS0000D590DF,RNACentral:URS0000D57655 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128488118..128488247 26863196 MeRIP-seq:(Medium) rs1248207209 Functional Loss SNV dbSNP153 33..33 33 - - - 99622 RMVar_ID_99622 Human_SNP_ID_152759023 m1A Human chr3 - 128489303 128489303 128489303 GGCGCTGCCCTGAACTGGCCTGGGAGGGGGTGACGGGGGCGCGCCCGCGGAGCTGGGCCCAGCCG GGCGCTGCCCTGAACTGGCCTGGGAGGGGGTGGCGGGGGCGCGCCCGCGGAGCTGGGCCCAGCCG T C GATA2 Ensembl:ENSG00000179348 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:128489253..128489431;chr3:128489253..128489543 26863196 MeRIP-seq:(Medium) rs1218498462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5654654 99623 RMVar_ID_99623 Human_SNP_ID_152759959 m1A Human chr3 + 128492465 128492465 128492465 TGCGGGGCGCAGCGCGCGGGGGCGCAAGCAGGAGCGAGCTGGGTTAAGCCGCGAAAAGCCGGCGC TGCGGGGCGCAGCGCGCGGGGGCGCAAGCAGGGGCGAGCTGGGTTAAGCCGCGAAAAGCCGGCGC A G GATA2-AS1 Ensembl:ENSG00000244300 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128492460..128492556 26863196 MeRIP-seq:(Medium) rs531238141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11171,Human_RBP_ID_266581,Human_RBP_ID_3720869,Human_RBP_ID_18499766,Human_RBP_ID_22745348 99624 RMVar_ID_99624 Human_SNP_ID_152761440 m1A Human chr3 - 128497798 128497798 128497798 GGGAAAATGGCTGCGGCGCTATCTGCGTCGCCATGGGGACCATCGCGCGCGCGCGGGCGGGGCGC GGGAAAATGGCTGCGGCGCTATCTGCGTCGCCGTGGGGACCATCGCGCGCGCGCGGGCGGGGCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:128497701..128497850 26863410 MeRIP-seq:(Medium) rs767119894 Functional Loss SNV dbSNP153 33..33 33 - - - 99625 RMVar_ID_99625 Human_SNP_ID_152761441 m1A Human chr3 - 128497798 128497798 128497798 GGGAAAATGGCTGCGGCGCTATCTGCGTCGCCATGGGGACCATCGCGCGCGCGCGGGCGGGGCGC GGGAAAATGGCTGCGGCGCTATCTGCGTCGCCCTGGGGACCATCGCGCGCGCGCGGGCGGGGCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:128497701..128497850 26863410 MeRIP-seq:(Medium) rs767119894 Functional Loss SNV dbSNP153 33..33 33 - - - 99626 RMVar_ID_99626 Human_SNP_ID_152761564 m1A Human chr3 - 128498142 128498142 128498142 GCACCTACTGTGTGTTAGTCTGGCCCTGGGGAACAGCAGTGACAAAGCAAAGCCCCTGCTCCCAG GCACCTACTGTGTGTTAGTCTGGCCCTGGGGAGCAGCAGTGACAAAGCAAAGCCCCTGCTCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128498093..128498214 26863196 MeRIP-seq:(Medium) rs1403236169 Functional Loss SNV dbSNP153 33..33 33 - - - 99627 RMVar_ID_99627 Human_SNP_ID_152771920 m1A Human chr3 - 128541657 128541653 128541657 TCATATAGCAAAAGCAGGAGCAAAAGAGAGAGAGAGTGGGAGGGGGTAGGTGGCACACACCTAAA TCATATAGCAAAAGCAGGAGCAAAAGAGAGAG____TGGGAGGGGGTAGGTGGCACACACCTAAA ACTCT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128541626..128541704 32194978 MeRIP-seq:(Medium) rs1229166933 Functional Loss DEL dbSNP153 33..36 33 - - - 99628 RMVar_ID_99628 Human_SNP_ID_152792876 m1A Human chr3 + 128622215 128622215 128622215 CCCTCTGTCTTCAGCCTGGACTGCAGCAGTGCAATCTCACTGGTCAAGGCCTTGTGTTCAGTCTC CCCTCTGTCTTCAGCCTGGACTGCAGCAGTGCTATCTCACTGGTCAAGGCCTTGTGTTCAGTCTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:128622117..128622337;chr3:128622151..128622225 26863196,32194978,32194978 MeRIP-seq:(Medium) rs1218015648 Functional Loss SNV dbSNP153 33..33 33 - - - 99629 RMVar_ID_99629 Human_SNP_ID_152794103 m1A Human chr3 - 128626738 128626738 128626738 TCTCTGACTGTGAAGATCATCCTGCCTGAAGGAGCCAAGTGAGTGTGACTGTTCCTCTCCTTTGC TCTCTGACTGTGAAGATCATCCTGCCTGAAGGGGCCAAGTGAGTGTGACTGTTCCTCTCCTTTGC T C RPN1 Ensembl:ENSG00000163902 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128626726..128626851 32194978 MeRIP-seq:(Medium) rs534311029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934485,Human_RBP_ID_1030853,Human_RBP_ID_1617247,Human_RBP_ID_1948704,Human_RBP_ID_3685405,Human_RBP_ID_5205923,Human_RBP_ID_7117946,Human_RBP_ID_8558001,Human_RBP_ID_9261148,Human_RBP_ID_9348907,Human_RBP_ID_14610017,Human_RBP_ID_17288138,Human_RBP_ID_18012915,Human_RBP_ID_18194700,Human_RBP_ID_20785166,Human_RBP_ID_22456153,Human_RBP_ID_22768965,Human_RBP_ID_23213589,Human_RBP_ID_23967739,Human_RBP_ID_27044835,Human_RBP_ID_27159654 Human_Splice_Rec_479848,Human_Splice_Rec_479849,Human_Splice_Rec_479866,Human_Splice_Rec_479867,Human_Splice_Rec_479875 RMVar_hsa_circ_118093,RMVar_hsa_circ_100765,RMVar_hsa_circ_104314,RMVar_hsa_circ_98650,RMVar_hsa_circ_27776,RMVar_hsa_circ_221064,RMVar_hsa_circ_87321,RMVar_hsa_circ_221065,RMVar_hsa_circ_221062,RMVar_hsa_circ_221063,RMVar_hsa_circ_221061,RMVar_hsa_circ_83781,RMVar_hsa_circ_374443,RMVar_hsa_circ_13238,RMVar_hsa_circ_283660,RMVar_hsa_circ_221071,RMVar_hsa_circ_221072,RMVar_hsa_circ_106437,RMVar_hsa_circ_268852,RMVar_hsa_circ_221073,RMVar_hsa_circ_221074 99630 RMVar_ID_99630 Human_SNP_ID_152797391 m1A Human chr3 - 128637915 128637915 128637915 TCTACTCTCCCTATCCAACGAAGACACAAACCATGCGTGTGAAGCTTGCCTCTCGAAATGTGGAG TCTACTCTCCCTATCCAACGAAGACACAAACCGTGCGTGTGAAGCTTGCCTCTCGAAATGTGGAG T C RPN1 Ensembl:ENSG00000163902 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128637866..128638041 26863196 MeRIP-seq:(Medium) rs773656479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68497,Human_RBP_ID_588690,Human_RBP_ID_938177,Human_RBP_ID_1948714,Human_RBP_ID_3685414,Human_RBP_ID_4760679,Human_RBP_ID_5299201,Human_RBP_ID_9131768,Human_RBP_ID_17291517,Human_RBP_ID_17404697,Human_RBP_ID_18013429,Human_RBP_ID_18796334,Human_RBP_ID_20816542,Human_RBP_ID_22456915,Human_RBP_ID_22768693,Human_RBP_ID_22821985,Human_RBP_ID_23967758,Human_RBP_ID_24495501,Human_RBP_ID_26824106,Human_RBP_ID_27313017 RMVar_hsa_circ_118093,RMVar_hsa_circ_100765,RMVar_hsa_circ_98650,RMVar_hsa_circ_221062,RMVar_hsa_circ_221063,RMVar_hsa_circ_221061,RMVar_hsa_circ_83781,RMVar_hsa_circ_268852,RMVar_hsa_circ_221073,RMVar_hsa_circ_221077,RMVar_hsa_circ_325123,RMVar_hsa_circ_361502,RMVar_hsa_circ_221076,RMVar_hsa_circ_221081,RMVar_hsa_circ_221080,RMVar_hsa_circ_315210,RMVar_hsa_circ_345550,RMVar_hsa_circ_221079,RMVar_hsa_circ_292848,RMVar_hsa_circ_300608,RMVar_hsa_circ_221082 99631 RMVar_ID_99631 Human_SNP_ID_152798113 m1A Human chr3 - 128640695 128640695 128640695 GGTATTGGGGACAGGGCAGAGTGAGGCATCAGAAGATGCCTGGGTTTCTAGCTTAGAGTTGATCA GGTATTGGGGACAGGGCAGAGTGAGGCATCAGGAGATGCCTGGGTTTCTAGCTTAGAGTTGATCA T C RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128640693..128640813 26863196 MeRIP-seq:(Medium) rs1487597082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118093,RMVar_hsa_circ_98650,RMVar_hsa_circ_221062,RMVar_hsa_circ_221061,RMVar_hsa_circ_83781,RMVar_hsa_circ_221073,RMVar_hsa_circ_221077,RMVar_hsa_circ_361502,RMVar_hsa_circ_221080,RMVar_hsa_circ_345550,RMVar_hsa_circ_300608,RMVar_hsa_circ_221082 99632 RMVar_ID_99632 Human_SNP_ID_152799267 m1A Human chr3 - 128644985 128644985 128644985 GACATGAATAATAAACTATCTTTTTCTGTTGTAGGTAAAGGGAGAAGATGAGGAAGAGAACAATT GACATGAATAATAAACTATCTTTTTCTGTTGTGGGTAAAGGGAGAAGATGAGGAAGAGAACAATT T C RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr3:128644976..128645000;chr3:128644951..128645000 26863196,32194978 MeRIP-seq:(Medium) rs200354372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68500,Human_RBP_ID_588697,Human_RBP_ID_933313,Human_RBP_ID_2747177,Human_RBP_ID_3685418,Human_RBP_ID_9348908 Human_Splice_Rec_479841,Human_Splice_Rec_479859,Human_Splice_Rec_479879,Human_Splice_Rec_479887,Human_Splice_Rec_479893 RMVar_hsa_circ_118093,RMVar_hsa_circ_221061 99633 RMVar_ID_99633 Human_SNP_ID_152799268 m1A Human chr3 - 128644985 128644985 128644985 GACATGAATAATAAACTATCTTTTTCTGTTGTAGGTAAAGGGAGAAGATGAGGAAGAGAACAATT GACATGAATAATAAACTATCTTTTTCTGTTGTCGGTAAAGGGAGAAGATGAGGAAGAGAACAATT T G RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr3:128644976..128645000;chr3:128644951..128645000 26863196,32194978 MeRIP-seq:(Medium) rs200354372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68500,Human_RBP_ID_588697,Human_RBP_ID_933313,Human_RBP_ID_2747177,Human_RBP_ID_3685418,Human_RBP_ID_9348908 Human_Splice_Rec_479841,Human_Splice_Rec_479859,Human_Splice_Rec_479879,Human_Splice_Rec_479887,Human_Splice_Rec_479893 RMVar_hsa_circ_118093,RMVar_hsa_circ_221061 99634 RMVar_ID_99634 Human_SNP_ID_152800848 m1A Human chr3 - 128650646 128650646 128650646 CCTAAGCAGCCACCTGGCTAAGGTGACGGCCGAGGTGGTCCTGGCGCACCTGGGCGGCGGCTCCA CCTAAGCAGCCACCTGGCTAAGGTGACGGCCGTGGTGGTCCTGGCGCACCTGGGCGGCGGCTCCA T A RPN1 Ensembl:ENSG00000163902 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:128650601..128650800 32194978 MeRIP-seq:(Medium) rs1427230616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68501,Human_RBP_ID_247598,Human_RBP_ID_588701,Human_RBP_ID_936576,Human_RBP_ID_1617281,Human_RBP_ID_4756712,Human_RBP_ID_8558028,Human_RBP_ID_8875619,Human_RBP_ID_22456158,Human_RBP_ID_23967780 RMVar_hsa_circ_118093,RMVar_hsa_circ_221061 99635 RMVar_ID_99635 Human_SNP_ID_152800918 m1A Human chr3 + 128650779 128650779 128650779 GGCCCAAGTCCCAAGCAACAGGAGCAGAAACAAGCCGGCGGCTGGCGCCTCCATGACCGGGAAGA GGCCCAAGTCCCAAGCAACAGGAGCAGAAACAGGCCGGCGGCTGGCGCCTCCATGACCGGGAAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:128650497..128650825;chr3:128644926..128650850;chr3:128644926..128650825 26863196 MeRIP-seq:(Medium) rs532290753 Functional Loss SNV dbSNP153 33..33 33 - - - 99636 RMVar_ID_99636 Human_SNP_ID_152821464 m1A Human chr3 - 128726276 128726276 128726276 CCGAGGAGGAGACTAAACGGAGGACAGAAGCGAGAAGGTCCAAGTTCTGGTTCCAGGGAACTCTC CCGAGGAGGAGACTAAACGGAGGACAGAAGCGGGAAGGTCCAAGTTCTGGTTCCAGGGAACTCTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:128726176..128795301 26863410 MeRIP-seq:(Medium) rs1019647432 Functional Loss SNV dbSNP153 33..33 33 - - - 99637 RMVar_ID_99637 Human_SNP_ID_152832447 m1A Human chr3 + 128767492 128767492 128767492 GGAGCCTGGGGTAAGGAAATAAATTAGGAGTCAAGAAGTAATGATGCAACTAGGATTGTGGAAAT GGAGCCTGGGGTAAGGAAATAAATTAGGAGTCGAGAAGTAATGATGCAACTAGGATTGTGGAAAT A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:128767490..128767717 26863196 MeRIP-seq:(Medium) rs1016703206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10065847,Human_RBP_ID_14611820 RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 99638 RMVar_ID_99638 Human_SNP_ID_152840310 m1A Human chr3 - 128797973 128797973 128797973 GCTTTGTACTGATTGCTGAATTTCTTATTCACATACTGGTTCATGAGTGATGTCTTCCCGACTCT GCTTTGTACTGATTGCTGAATTTCTTATTCACGTACTGGTTCATGAGTGATGTCTTCCCGACTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128797970..128798070 32194978 MeRIP-seq:(Medium) rs1301670871 Functional Loss SNV dbSNP153 33..33 33 - - - 99639 RMVar_ID_99639 Human_SNP_ID_152840316 m1A Human chr3 + 128797993 128797993 128797993 CATGAACCAGTATGTGAATAAGAAATTCAGCAATCAGTACAAAGCCACAATAGGAGCTGACTTTC CATGAACCAGTATGTGAATAAGAAATTCAGCAGTCAGTACAAAGCCACAATAGGAGCTGACTTTC A G RAB7A Ensembl:ENSG00000075785 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:128797897..128798075;chr3:128797879..128798025 26863196 MeRIP-seq:(Medium) rs747270770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66728,Human_RBP_ID_588717,Human_RBP_ID_1617323,Human_RBP_ID_1948769,Human_RBP_ID_4758890,Human_RBP_ID_8558114,Human_RBP_ID_9131796,Human_RBP_ID_9394058,Human_RBP_ID_21898341,Human_RBP_ID_23967920 Human_Splice_Rec_479904,Human_Splice_Rec_479905,Human_Splice_Rec_479914,Human_Splice_Rec_479915,Human_Splice_Rec_479924,Human_Splice_Rec_479926,Human_Splice_Rec_479927,Human_Splice_Rec_479932,Human_Splice_Rec_479933,Human_Splice_Rec_479936,Human_Splice_Rec_479937,Human_Splice_Rec_479942,Human_Splice_Rec_479943,Human_Splice_Rec_479948,Human_Splice_Rec_479949 RMVar_hsa_circ_7841,RMVar_hsa_circ_221086,RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084,RMVar_hsa_circ_276515,RMVar_hsa_circ_285686,RMVar_hsa_circ_378866,RMVar_hsa_circ_102059,RMVar_hsa_circ_106637,RMVar_hsa_circ_221087,RMVar_hsa_circ_221089,RMVar_hsa_circ_221090,RMVar_hsa_circ_221088,RMVar_hsa_circ_114706,RMVar_hsa_circ_315067,RMVar_hsa_circ_221092,RMVar_hsa_circ_19022,RMVar_hsa_circ_221093,RMVar_hsa_circ_221091 99640 RMVar_ID_99640 Human_SNP_ID_152844285 m1A Human chr3 + 128813597 128813597 128813597 AGTTACACCCCACATATCTCTCACACACACACACACACGCACACACACACACACAGATCTGACGT AGTTACACCCCACATATCTCTCACACACACACGCACACGCACACACACACACACAGATCTGACGT A G RAB7A Ensembl:ENSG00000075785 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128813305..128813747 26863196 MeRIP-seq:(Medium) rs1303516654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212713,Human_RBP_ID_2747450,Human_RBP_ID_9435453,Human_RBP_ID_17288153,Human_RBP_ID_17401562,Human_RBP_ID_17517016,Human_RBP_ID_24535454,Human_RBP_ID_26511710 Human_miRNA_ID_323796,Human_miRNA_ID_2205755 RMVar_hsa_circ_112866,RMVar_hsa_circ_221084,RMVar_hsa_circ_102059,RMVar_hsa_circ_97431,RMVar_hsa_circ_221090,RMVar_hsa_circ_114706,RMVar_hsa_circ_221091,RMVar_hsa_circ_87392,RMVar_hsa_circ_221096,RMVar_hsa_circ_123322,RMVar_hsa_circ_221097,RMVar_hsa_circ_221098 99641 RMVar_ID_99641 Human_SNP_ID_152860741 m1A Human chr3 - 128879683 128879683 128879683 CAGGAAGAGCCCGCAGCCGCTCATGCTGCCCGATGTTCCCCAGCCTCAGCCTCAGTCTCCCCTTC CAGGAAGAGCCCGCAGCCGCTCATGCTGCCCGGTGTTCCCCAGCCTCAGCCTCAGTCTCCCCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128879635..128879770 26863196 MeRIP-seq:(Medium) rs745859672 Functional Loss SNV dbSNP153 33..33 33 - - - 99642 RMVar_ID_99642 Human_SNP_ID_152865166 m1A Human chr3 + 128896473 128896473 128896473 CATCTTGGCTGGCACTGAGGAGCAGAAAGCCAAATACTTGCCTAAACTGGCGTCCGGGGAGCACA CATCTTGGCTGGCACTGAGGAGCAGAAAGCCAGATACTTGCCTAAACTGGCGTCCGGGGAGCACA A G ACAD9 Ensembl:ENSG00000177646 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:128895357..128896476 32194978 MeRIP-seq:(Medium) rs759184803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18796477,Human_RBP_ID_19010857,Human_RBP_ID_27822469 Human_Splice_Rec_479970,Human_Splice_Rec_479971,Human_Splice_Rec_479982,Human_Splice_Rec_479983,Human_Splice_Rec_479994,Human_Splice_Rec_479995,Human_Splice_Rec_480026,Human_Splice_Rec_480027,Human_Splice_Rec_480050,Human_Splice_Rec_480051,Human_Splice_Rec_480088,Human_Splice_Rec_480094,Human_Splice_Rec_480095 RMVar_hsa_circ_9334,RMVar_hsa_circ_78808,RMVar_hsa_circ_324259,RMVar_hsa_circ_221099,RMVar_hsa_circ_343078,RMVar_hsa_circ_121050,RMVar_hsa_circ_267738,RMVar_hsa_circ_221100,RMVar_hsa_circ_221101,RMVar_hsa_circ_348428,RMVar_hsa_circ_358372,RMVar_hsa_circ_329422,RMVar_hsa_circ_36709,RMVar_hsa_circ_45862,RMVar_hsa_circ_25826,RMVar_hsa_circ_221102 99643 RMVar_ID_99643 Human_SNP_ID_152867813 m1A Human chr3 - 128906187 128906187 128906187 CAGTATGCGCTCGTACGGATAGTCCCTTGTGTAGCCCAAGCCCCCGAGGATCTGCAGCGCCTCAC CAGTATGCGCTCGTACGGATAGTCCCTTGTGTGGCCCAAGCCCCCGAGGATCTGCAGCGCCTCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:128906101..128906287;chr3:128906126..128906279 26863196 MeRIP-seq:(Medium) rs1559829157 Functional Loss SNV dbSNP153 33..33 33 - - - 99644 RMVar_ID_99644 Human_SNP_ID_152867821 m1A Human chr3 - 128906201 128906201 128906201 ATGCGGGTGTCACGCAGTATGCGCTCGTACGGATAGTCCCTTGTGTAGCCCAAGCCCCCGAGGAT ATGCGGGTGTCACGCAGTATGCGCTCGTACGGGTAGTCCCTTGTGTAGCCCAAGCCCCCGAGGAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:128906152..128908287 32194978 MeRIP-seq:(Medium) rs1243971835 Functional Loss SNV dbSNP153 33..33 33 - - - 99645 RMVar_ID_99645 Human_SNP_ID_152867985 m1A Human chr3 - 128906706 128906706 128906706 CTTCATTCACCTTGTGCCAGCAGATCAGTCCCATCTGGGCCTGGCGCGCTCTATTACCCTGCCCT CTTCATTCACCTTGTGCCAGCAGATCAGTCCCCTCTGGGCCTGGCGCGCTCTATTACCCTGCCCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128906703..128907145 26863196 MeRIP-seq:(Medium) rs1173509607 Functional Loss SNV dbSNP153 33..33 33 - - - 99646 RMVar_ID_99646 Human_SNP_ID_152868400 m1A Human chr3 + 128908251 128908251 128908251 TGACGGGTCTGCAGCATGCCGGCCGCATCCTGACTACCAGGATCCAGTAGGTGCCATTGTCACCG TGACGGGTCTGCAGCATGCCGGCCGCATCCTGGCTACCAGGATCCAGTAGGTGCCATTGTCACCG A G ACAD9 Ensembl:ENSG00000177646 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:128908149..128908284;chr3:128908176..128908275 26863196 MeRIP-seq:(Medium) rs1451444183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_480010,Human_Splice_Rec_480011,Human_Splice_Rec_480042,Human_Splice_Rec_480066,Human_Splice_Rec_480067,Human_Splice_Rec_480110,Human_Splice_Rec_480111,Human_Splice_Rec_480134,Human_Splice_Rec_480135,Human_Splice_Rec_480156,Human_Splice_Rec_480157,Human_Splice_Rec_480178,Human_Splice_Rec_480179 RMVar_hsa_circ_78808,RMVar_hsa_circ_221099,RMVar_hsa_circ_79285,RMVar_hsa_circ_221106,RMVar_hsa_circ_46541 99647 RMVar_ID_99647 Human_SNP_ID_152868401 m1A Human chr3 + 128908257 128908257 128908257 GTCTGCAGCATGCCGGCCGCATCCTGACTACCAGGATCCAGTAGGTGCCATTGTCACCGTGTGCT GTCTGCAGCATGCCGGCCGCATCCTGACTACCGGGATCCAGTAGGTGCCATTGTCACCGTGTGCT A G ACAD9 Ensembl:ENSG00000177646 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:128908186..128908287 32194978 MeRIP-seq:(Medium) rs769920112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_480010,Human_Splice_Rec_480011,Human_Splice_Rec_480042,Human_Splice_Rec_480066,Human_Splice_Rec_480067,Human_Splice_Rec_480110,Human_Splice_Rec_480111,Human_Splice_Rec_480134,Human_Splice_Rec_480135,Human_Splice_Rec_480156,Human_Splice_Rec_480157,Human_Splice_Rec_480178,Human_Splice_Rec_480179 RMVar_hsa_circ_78808,RMVar_hsa_circ_221099,RMVar_hsa_circ_79285,RMVar_hsa_circ_221106,RMVar_hsa_circ_46541 99648 RMVar_ID_99648 Human_SNP_ID_152868640 m1A Human chr3 + 128908955 128908955 128908955 TGAGCGCCAGCAGCGAGGCCTCCAGTCACAGGACCATGGACTTTCTGCAGTGAGCTTAAACAGGC TGAGCGCCAGCAGCGAGGCCTCCAGTCACAGGGCCATGGACTTTCTGCAGTGAGCTTAAACAGGC A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128908951..128909000 26863196 MeRIP-seq:(Medium) rs1352172179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8558215,Human_RBP_ID_14614235 RMVar_hsa_circ_78808,RMVar_hsa_circ_221099,RMVar_hsa_circ_79285,RMVar_hsa_circ_221106,RMVar_hsa_circ_46541 99649 RMVar_ID_99649 Human_SNP_ID_152914033 m1A Human chr3 + 129090170 129090170 129090170 CCTCTCCTTTTTTGTCTGGGAGACTCGATTCCATAGACTGGGACCCACGCTCGGCTGGCAGGATT CCTCTCCTTTTTTGTCTGGGAGACTCGATTCCGTAGACTGGGACCCACGCTCGGCTGGCAGGATT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129090107..129090207 32194978 MeRIP-seq:(Medium) rs1262280048 Functional Loss SNV dbSNP153 33..33 33 - - - 99650 RMVar_ID_99650 Human_SNP_ID_152918327 m1A Human chr3 + 129107903 129107901 129107904 CCTCACCCTCCAAGCCACTCGGTCACCTCTTCAACTCTCTAGAGCAAACCCTCCTCCCCGGGCTC CCTCACCCTCCAAGCCACTCGGTCACCTCTT___CTCTCTAGAGCAAACCCTCCTCCCCGGGCTC TCAA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129107819..129107990 26863196 MeRIP-seq:(Medium) rs1319506772 Functional Loss DEL dbSNP153 32..34 33 - - - 99651 RMVar_ID_99651 Human_SNP_ID_152918328 m1A Human chr3 + 129107903 129107903 129107903 CCTCACCCTCCAAGCCACTCGGTCACCTCTTCAACTCTCTAGAGCAAACCCTCCTCCCCGGGCTC CCTCACCCTCCAAGCCACTCGGTCACCTCTTCCACTCTCTAGAGCAAACCCTCCTCCCCGGGCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129107819..129107990 26863196 MeRIP-seq:(Medium) rs1280513295 Functional Loss SNV dbSNP153 33..33 33 - - - 99652 RMVar_ID_99652 Human_SNP_ID_152921885 m1A Human chr3 + 129122038 129122038 129122038 ACTCTGCCCTCAGCCCGACCTCGACTCCGCCCACAGGACCACCTCAGCCCGCCCCGACTCCGCCC ACTCTGCCCTCAGCCCGACCTCGACTCCGCCCCCAGGACCACCTCAGCCCGCCCCGACTCCGCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129121371..129122552 26863196 MeRIP-seq:(Medium) rs1202190088 Functional Loss SNV dbSNP153 33..33 33 - - - 99653 RMVar_ID_99653 Human_SNP_ID_152931761 m1A Human chr3 - 129158547 129158547 129158547 ATCTTTTATATCGCTGGTAGGACGGCCTTAGCAAGATTTCGCCAGGCTCAGCTGGAAGAGGGAAA ATCTTTTATATCGCTGGTAGGACGGCCTTAGCCAGATTTCGCCAGGCTCAGCTGGAAGAGGGAAA T G ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129156909..129161046 26863196 MeRIP-seq:(Medium) rs1203370111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933318,Human_RBP_ID_4757435,Human_RBP_ID_5390242,Human_RBP_ID_9348911 Human_Splice_Rec_480364,Human_Splice_Rec_480365,Human_Splice_Rec_480388,Human_Splice_Rec_480389,Human_Splice_Rec_480418,Human_Splice_Rec_480419,Human_Splice_Rec_480450,Human_Splice_Rec_480451,Human_Splice_Rec_480470,Human_Splice_Rec_480471 RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 99654 RMVar_ID_99654 Human_SNP_ID_152932386 m1A Human chr3 + 129160938 129160937 129160939 GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCCATCCACTCGCTCCCTCACCCGCCCACCCTACTC GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCC__CCACTCGCTCCCTCACCCGCCCACCCTACTC CAT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:129160927..129161064 26863410 MeRIP-seq:(Medium) rs752861161 Functional Loss DEL dbSNP153 33..34 33 - - - 99655 RMVar_ID_99655 Human_SNP_ID_152932388 m1A Human chr3 + 129160938 129160938 129160938 GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCCATCCACTCGCTCCCTCACCCGCCCACCCTACTC GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCCCTCCACTCGCTCCCTCACCCGCCCACCCTACTC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:129160927..129161064 26863410 MeRIP-seq:(Medium) rs748694623 Functional Loss SNV dbSNP153 33..33 33 - - - 99656 RMVar_ID_99656 Human_SNP_ID_152932389 m1A Human chr3 + 129160938 129160938 129160938 GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCCATCCACTCGCTCCCTCACCCGCCCACCCTACTC GGTGGACTGGGCGCCCCCCCGCCCGCCCGCCCGTCCACTCGCTCCCTCACCCGCCCACCCTACTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:129160927..129161064 26863410 MeRIP-seq:(Medium) rs748694623 Functional Loss SNV dbSNP153 33..33 33 - - - 99657 RMVar_ID_99657 Human_SNP_ID_152932444 m1A Human chr3 - 129161015 129161015 129161015 GGCGTCTTCTGGGCCTGTGGAGTTTCTTGGACAGGGGCCGCGGGGCTCCAGGACGGCGCCCTTAG GGCGTCTTCTGGGCCTGTGGAGTTTCTTGGACGGGGGCCGCGGGGCTCCAGGACGGCGCCCTTAG T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:129158507..129161046 26863196 MeRIP-seq:(Medium) rs1448743376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247997,Human_RBP_ID_836943,Human_RBP_ID_4721919,Human_RBP_ID_5505463,Human_RBP_ID_27822474 Human_Splice_Rec_480361,Human_Splice_Rec_480385,Human_Splice_Rec_480415,Human_Splice_Rec_480447,Human_Splice_Rec_480467 Human_miRNA_ID_2443575 RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 99658 RMVar_ID_99658 Human_SNP_ID_152932449 m1A Human chr3 + 129161024 129161024 129161024 CCGTCCTGGAGCCCCGCGGCCCCTGTCCAAGAAACTCCACAGGCCCAGAAGACGCCGACGCTCAC CCGTCCTGGAGCCCCGCGGCCCCTGTCCAAGATACTCCACAGGCCCAGAAGACGCCGACGCTCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129158556..129161049 26863196 MeRIP-seq:(Medium) rs1341052177 Functional Loss SNV dbSNP153 33..33 33 - - - 99659 RMVar_ID_99659 Human_SNP_ID_152935401 m1A Human chr3 - 129169889 129169889 129169889 ATCGGAATAAAAGCCTAAACAGGAACAACTTCATCACAGTGTTGATGTTGGACACATAGATGGTG ATCGGAATAAAAGCCTAAACAGGAACAACTTCGTCACAGTGTTGATGTTGGACACATAGATGGTG T C CNBP Ensembl:ENSG00000169714 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129169838..129169972 26863196 MeRIP-seq:(Medium) rs984922528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588961,Human_RBP_ID_1030924,Human_RBP_ID_1617609,Human_RBP_ID_1948928,Human_RBP_ID_2747738,Human_RBP_ID_3685743,Human_RBP_ID_7119183,Human_RBP_ID_8558358,Human_RBP_ID_8867770,Human_RBP_ID_14616398,Human_RBP_ID_17288195,Human_RBP_ID_17401605,Human_RBP_ID_17517059,Human_RBP_ID_17993773,Human_RBP_ID_18332440,Human_RBP_ID_22508698,Human_RBP_ID_23968313,Human_RBP_ID_27711625 Human_miRNA_ID_2059173,Human_miRNA_ID_2184568 RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 99660 RMVar_ID_99660 Human_SNP_ID_152935564 m1A Human chr3 - 129170483 129170483 129170483 TGTTACCGCTGTGGCGAGTCAGGGCACCTTGCACGGGAATGCACAATTGAGGCTACAGCCTAATT TGTTACCGCTGTGGCGAGTCAGGGCACCTTGCGCGGGAATGCACAATTGAGGCTACAGCCTAATT T C CNBP Ensembl:ENSG00000169714 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129170434..129170563 26863196 MeRIP-seq:(Medium) rs1433919972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588984,Human_RBP_ID_783897,Human_RBP_ID_1030942,Human_RBP_ID_1203278,Human_RBP_ID_1383799,Human_RBP_ID_1617628,Human_RBP_ID_1948940,Human_RBP_ID_4721963,Human_RBP_ID_7119225,Human_RBP_ID_8558380,Human_RBP_ID_9131884,Human_RBP_ID_14616437,Human_RBP_ID_17288209,Human_RBP_ID_22455557,Human_RBP_ID_22768974,Human_RBP_ID_22822071,Human_RBP_ID_23017849,Human_RBP_ID_23968332,Human_RBP_ID_25695662,Human_RBP_ID_26824108,Human_RBP_ID_27045146,Human_RBP_ID_27313130 Human_Splice_Rec_480492,Human_Splice_Rec_480500,Human_Splice_Rec_480506,Human_Splice_Rec_480512,Human_Splice_Rec_480520,Human_Splice_Rec_480528,Human_Splice_Rec_480534,Human_Splice_Rec_480540 RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 99661 RMVar_ID_99661 Human_SNP_ID_152935724 m1A Human chr3 - 129171232 129171232 129171232 CGGTAGAGGTGGCCACATTGCCAAGGACTGCAAGGAGCCCAAGAGAGAGCGAGAGCAATGCTGCT CGGTAGAGGTGGCCACATTGCCAAGGACTGCAGGGAGCCCAAGAGAGAGCGAGAGCAATGCTGCT T C CNBP Ensembl:ENSG00000169714 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129171053..129171286 26863196 MeRIP-seq:(Medium) rs774926505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247744,Human_RBP_ID_588993,Human_RBP_ID_836899,Human_RBP_ID_934490,Human_RBP_ID_1030952,Human_RBP_ID_1617653,Human_RBP_ID_1948950,Human_RBP_ID_3685753,Human_RBP_ID_5209868,Human_RBP_ID_7119240,Human_RBP_ID_8558386,Human_RBP_ID_14616477,Human_RBP_ID_18012924,Human_RBP_ID_18796628,Human_RBP_ID_22455558,Human_RBP_ID_22822077,Human_RBP_ID_23134758,Human_RBP_ID_23968344,Human_RBP_ID_26503472,Human_RBP_ID_27045153,Human_RBP_ID_27313136 Human_Splice_Rec_480490,Human_Splice_Rec_480498,Human_Splice_Rec_480518,Human_Splice_Rec_480526,Human_Splice_Rec_480546 RMVar_hsa_circ_18502,RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 99662 RMVar_ID_99662 Human_SNP_ID_152935731 m1A Human chr3 + 129171261 129171261 129171261 TCCTTGCAGTCCTTGGCAATGTGGCCACCTCTACCGCAGTTATAGCAGGCTTCAACAATAAGGAA TCCTTGCAGTCCTTGGCAATGTGGCCACCTCTCCCGCAGTTATAGCAGGCTTCAACAATAAGGAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129169776..129171300 32194978 MeRIP-seq:(Medium) rs879137907 Functional Loss SNV dbSNP153 33..33 33 - - - 99663 RMVar_ID_99663 Human_SNP_ID_152935900 m1A Human chr3 - 129171771 129171771 129171771 GGTTTAATGCTGTTACTTTTAATATTTCAAAGATCTGACTGCAGCCATGAGCAGCAATGAGTGCT GGTTTAATGCTGTTACTTTTAATATTTCAAAGGTCTGACTGCAGCCATGAGCAGCAATGAGTGCT T C CNBP Ensembl:ENSG00000169714 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129171726..129171775 32194978 MeRIP-seq:(Medium) rs1354890881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247747,Human_RBP_ID_589000,Human_RBP_ID_939284,Human_RBP_ID_1617670,Human_RBP_ID_1948957,Human_RBP_ID_2747756,Human_RBP_ID_4757439,Human_RBP_ID_9131897,Human_RBP_ID_14616491,Human_RBP_ID_18796635,Human_RBP_ID_25695677,Human_RBP_ID_26678309 Human_Splice_Rec_480486,Human_Splice_Rec_480494,Human_Splice_Rec_480502,Human_Splice_Rec_480508,Human_Splice_Rec_480514,Human_Splice_Rec_480522,Human_Splice_Rec_480530,Human_Splice_Rec_480536,Human_Splice_Rec_480542,Human_Splice_Rec_480548 RMVar_hsa_circ_76874,RMVar_hsa_circ_221109,RMVar_hsa_circ_95420,RMVar_hsa_circ_363622,RMVar_hsa_circ_221112,RMVar_hsa_circ_221113 99664 RMVar_ID_99664 Human_SNP_ID_152939738 m1A Human chr3 - 129183262 129183262 129183262 GCGGGCCATGTGCCAAGGGTTTTGGGGGCCTTAGAAAAGGGTTCTTAGGCCGGGCGCGGTGGCTC GCGGGCCATGTGCCAAGGGTTTTGGGGGCCTTTGAAAAGGGTTCTTAGGCCGGGCGCGGTGGCTC T A CNBP Ensembl:ENSG00000169714 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129183259..129183487 26863196 MeRIP-seq:(Medium) rs1451179666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 99665 RMVar_ID_99665 Human_SNP_ID_152939749 m1A Human chr3 + 129183284 129183284 129183284 AACCCTTTTCTAAGGCCCCCAAAACCCTTGGCACATGGCCCGCCAGGCGCACGACCCCAGCACAT AACCCTTTTCTAAGGCCCCCAAAACCCTTGGCCCATGGCCCGCCAGGCGCACGACCCCAGCACAT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:129183269..129183550 26863196 MeRIP-seq:(Medium) rs978967886 Functional Loss SNV dbSNP153 33..33 33 - - - 99666 RMVar_ID_99666 Human_SNP_ID_152956794 m1A Human chr3 + 129249741 129249741 129249741 TATGTTGAAGAAATTCGACAAGAAGGATGAGGAGTCAGGTGAGGGGGCCAGGCCTGGGTCTGAGG TATGTTGAAGAAATTCGACAAGAAGGATGAGGGGTCAGGTGAGGGGGCCAGGCCTGGGTCTGAGG A G COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:129249660..129249777 26863410 MeRIP-seq:(Medium) rs1274961908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757443,Human_RBP_ID_22606490,Human_RBP_ID_27823474 Human_Splice_Rec_480549,Human_Splice_Rec_480591,Human_Splice_Rec_480595,Human_Splice_Rec_480635 99667 RMVar_ID_99667 Human_SNP_ID_152957759 m1A Human chr3 - 129252696 129252696 129252696 CACCTCTCAAGGAAAGCTGGGTTGAGGCACTTACATCATTGGACTGAAAGAGCTTGGTCATGGCA CACCTCTCAAGGAAAGCTGGGTTGAGGCACTTGCATCATTGGACTGAAAGAGCTTGGTCATGGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129252601..129252700 32194978 MeRIP-seq:(Medium) rs776252517 Functional Loss SNV dbSNP153 33..33 33 - - - 99668 RMVar_ID_99668 Human_SNP_ID_152959194 m1A Human chr3 + 129257840 129257840 129257840 CATCGTCAATCTGCCAGGCTGCAGTGCCAAAGAGCTGGCCCCGGCTGTGTCAGGTCACTGGGCAT CATCGTCAATCTGCCAGGCTGCAGTGCCAAAGGGCTGGCCCCGGCTGTGTCAGGTCACTGGGCAT A G COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129257791..129257885 26863196 MeRIP-seq:(Medium) rs1194813518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26824947 Human_Splice_Rec_480563,Human_Splice_Rec_480607 Human_miRNA_ID_2661383,Human_miRNA_ID_2679832 RMVar_hsa_circ_56514,RMVar_hsa_circ_118205,RMVar_hsa_circ_325848,RMVar_hsa_circ_88123,RMVar_hsa_circ_221116,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_374379,RMVar_hsa_circ_109173,RMVar_hsa_circ_124012,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_221127,RMVar_hsa_circ_14623,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221126,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_221134,RMVar_hsa_circ_101148,RMVar_hsa_circ_118134,RMVar_hsa_circ_221132,RMVar_hsa_circ_221133,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135 99669 RMVar_ID_99669 Human_SNP_ID_152959932 m1A Human chr3 + 129260797 129260797 129260797 GCAGATCTCCTCCTTCATGTCAGAAATCTCGGATGAATTCAAGGTACCTGCTACCCCCAGGACAC GCAGATCTCCTCCTTCATGTCAGAAATCTCGGGTGAATTCAAGGTACCTGCTACCCCCAGGACAC A G COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129260601..129260825 32194978 MeRIP-seq:(Medium) rs1331721121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19118406 Human_Splice_Rec_480567,Human_Splice_Rec_480611,Human_Splice_Rec_480649 RMVar_hsa_circ_56514,RMVar_hsa_circ_118205,RMVar_hsa_circ_325848,RMVar_hsa_circ_88123,RMVar_hsa_circ_221116,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_374379,RMVar_hsa_circ_109173,RMVar_hsa_circ_124012,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_221127,RMVar_hsa_circ_14623,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221126,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_85666,RMVar_hsa_circ_118134,RMVar_hsa_circ_221132,RMVar_hsa_circ_221133,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_221138,RMVar_hsa_circ_358260,RMVar_hsa_circ_358679,RMVar_hsa_circ_378587,RMVar_hsa_circ_355779,RMVar_hsa_circ_221136,RMVar_hsa_circ_221137,RMVar_hsa_circ_121699,RMVar_hsa_circ_221140,RMVar_hsa_circ_53515,RMVar_hsa_circ_221139 99670 RMVar_ID_99670 Human_SNP_ID_152961150 m1A Human chr3 + 129265692 129265692 129265692 TGCGAGTTCACAGTGCTGGCCACCCGTATTCTACATCTCCTGGGCCAGGAGGGGCCCAAGACCAC TGCGAGTTCACAGTGCTGGCCACCCGTATTCTCCATCTCCTGGGCCAGGAGGGGCCCAAGACCAC A C COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129265526..129265800 32194978 MeRIP-seq:(Medium) rs1024737188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69351,Human_RBP_ID_247937,Human_RBP_ID_784184,Human_RBP_ID_4760844,Human_RBP_ID_9301113,Human_RBP_ID_17702803,Human_RBP_ID_17993808,Human_RBP_ID_20785209,Human_RBP_ID_22455565,Human_RBP_ID_22768704 Human_Splice_Rec_480657 Human_miRNA_ID_2992256 RMVar_hsa_circ_56514,RMVar_hsa_circ_118205,RMVar_hsa_circ_325848,RMVar_hsa_circ_88123,RMVar_hsa_circ_221116,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_374379,RMVar_hsa_circ_109173,RMVar_hsa_circ_124012,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_221127,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221126,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_85666,RMVar_hsa_circ_118134,RMVar_hsa_circ_221132,RMVar_hsa_circ_221133,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_378587,RMVar_hsa_circ_355779,RMVar_hsa_circ_221136,RMVar_hsa_circ_121699,RMVar_hsa_circ_91516,RMVar_hsa_circ_221140,RMVar_hsa_circ_221141,RMVar_hsa_circ_221139,RMVar_hsa_circ_294348,RMVar_hsa_circ_274866,RMVar_hsa_circ_221143,RMVar_hsa_circ_88092,RMVar_hsa_circ_221144,RMVar_hsa_circ_221142 99671 RMVar_ID_99671 Human_SNP_ID_152961732 m1A Human chr3 - 129267896 129267896 129267896 AGGACACAAGGTGGTCCTGACTGGGACCCAGCAGGGATGGCAGGAGGGATCCTGCATGGCTTCAT AGGACACAAGGTGGTCCTGACTGGGACCCAGCCGGGATGGCAGGAGGGATCCTGCATGGCTTCAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129267891..129268074 26863196 MeRIP-seq:(Medium) rs1229689630 Functional Loss SNV dbSNP153 33..33 33 - - - 99672 RMVar_ID_99672 Human_SNP_ID_152961908 m1A Human chr3 + 129268576 129268576 129268576 TCTAGAACCATCAGAAAAACCTTTTGACCTCAAGTCTGTGCCCCTGGCCACGGCGCCCATGGCAG TCTAGAACCATCAGAAAAACCTTTTGACCTCACGTCTGTGCCCCTGGCCACGGCGCCCATGGCAG A C COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129268476..129268625 32194978 MeRIP-seq:(Medium) rs751992693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965450,Human_RBP_ID_14617325,Human_RBP_ID_17702805,Human_RBP_ID_22455567 Human_Splice_Rec_480576,Human_Splice_Rec_480577,Human_Splice_Rec_480620,Human_Splice_Rec_480621 Human_miRNA_ID_2027026,Human_miRNA_ID_2744721 RMVar_hsa_circ_88123,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_109173,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_61766,RMVar_hsa_circ_221132,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_378587,RMVar_hsa_circ_221136,RMVar_hsa_circ_121699,RMVar_hsa_circ_91516,RMVar_hsa_circ_221140,RMVar_hsa_circ_221143,RMVar_hsa_circ_88092,RMVar_hsa_circ_221144,RMVar_hsa_circ_221145,RMVar_hsa_circ_221146,RMVar_hsa_circ_329196 99673 RMVar_ID_99673 Human_SNP_ID_152961909 m1A Human chr3 + 129268576 129268576 129268576 TCTAGAACCATCAGAAAAACCTTTTGACCTCAAGTCTGTGCCCCTGGCCACGGCGCCCATGGCAG TCTAGAACCATCAGAAAAACCTTTTGACCTCAGGTCTGTGCCCCTGGCCACGGCGCCCATGGCAG A G COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129268476..129268625 32194978 MeRIP-seq:(Medium) rs751992693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3965450,Human_RBP_ID_14617325,Human_RBP_ID_17702805,Human_RBP_ID_22455567 Human_Splice_Rec_480576,Human_Splice_Rec_480577,Human_Splice_Rec_480620,Human_Splice_Rec_480621 Human_miRNA_ID_2027026,Human_miRNA_ID_2744721 RMVar_hsa_circ_88123,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_109173,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_61766,RMVar_hsa_circ_221132,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_378587,RMVar_hsa_circ_221136,RMVar_hsa_circ_121699,RMVar_hsa_circ_91516,RMVar_hsa_circ_221140,RMVar_hsa_circ_221143,RMVar_hsa_circ_88092,RMVar_hsa_circ_221144,RMVar_hsa_circ_221145,RMVar_hsa_circ_221146,RMVar_hsa_circ_329196 99674 RMVar_ID_99674 Human_SNP_ID_152961925 m1A Human chr3 + 129268607 129268607 129268607 AAGTCTGTGCCCCTGGCCACGGCGCCCATGGCAGAGCAGAGAACAGGTAACACTTATACTCCTCC AAGTCTGTGCCCCTGGCCACGGCGCCCATGGCGGAGCAGAGAACAGGTAACACTTATACTCCTCC A G COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129268500..129268652 26863196 MeRIP-seq:(Medium) rs754098659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784186,Human_RBP_ID_3965450,Human_RBP_ID_9302487,Human_RBP_ID_22457468,Human_RBP_ID_22768979 Human_Splice_Rec_480577,Human_Splice_Rec_480621 Human_miRNA_ID_2394612,Human_miRNA_ID_2906630,Human_miRNA_ID_3025462 RMVar_hsa_circ_88123,RMVar_hsa_circ_221117,RMVar_hsa_circ_88630,RMVar_hsa_circ_109173,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_78300,RMVar_hsa_circ_221125,RMVar_hsa_circ_221124,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_61766,RMVar_hsa_circ_221132,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_378587,RMVar_hsa_circ_221136,RMVar_hsa_circ_121699,RMVar_hsa_circ_91516,RMVar_hsa_circ_221140,RMVar_hsa_circ_221143,RMVar_hsa_circ_88092,RMVar_hsa_circ_221144,RMVar_hsa_circ_221145,RMVar_hsa_circ_221146,RMVar_hsa_circ_329196 99675 RMVar_ID_99675 Human_SNP_ID_152962783 m1A Human chr3 + 129272320 129272320 129272320 CACAGTGCAGATGGAGCCCACTGAGGCCTATGAGGTGCTCTGTTACGTGCCTGCCCGGAGCCTGC CACAGTGCAGATGGAGCCCACTGAGGCCTATGTGGTGCTCTGTTACGTGCCTGCCCGGAGCCTGC A T COPG1 Ensembl:ENSG00000181789 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs758107103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156290,Human_RBP_ID_5150168 Human_Splice_Rec_480582,Human_Splice_Rec_480583,Human_Splice_Rec_480626,Human_Splice_Rec_480627,Human_Splice_Rec_480659,Human_Splice_Rec_480667 Human_miRNA_ID_2160537,Human_miRNA_ID_2491187 RMVar_hsa_circ_88123,RMVar_hsa_circ_221117,RMVar_hsa_circ_109173,RMVar_hsa_circ_98884,RMVar_hsa_circ_221123,RMVar_hsa_circ_221122,RMVar_hsa_circ_108488,RMVar_hsa_circ_61766,RMVar_hsa_circ_221132,RMVar_hsa_circ_84151,RMVar_hsa_circ_221135,RMVar_hsa_circ_378587,RMVar_hsa_circ_221136,RMVar_hsa_circ_121699,RMVar_hsa_circ_91516,RMVar_hsa_circ_221140,RMVar_hsa_circ_221143,RMVar_hsa_circ_88092,RMVar_hsa_circ_221144,RMVar_hsa_circ_221145,RMVar_hsa_circ_221146,RMVar_hsa_circ_329196,RMVar_hsa_circ_98612,RMVar_hsa_circ_89123,RMVar_hsa_circ_221147,RMVar_hsa_circ_100307,RMVar_hsa_circ_221148,RMVar_hsa_circ_221149 99676 RMVar_ID_99676 Human_SNP_ID_152964701 m1A Human chr3 - 129279790 129279790 129279790 CGGGAGCCGCTGCTGGCCCCGCCGATCCTGGTAGGCGCAAGCTCTCGTGAGAACATCTCTAGGTA CGGGAGCCGCTGCTGGCCCCGCCGATCCTGGTGGGCGCAAGCTCTCGTGAGAACATCTCTAGGTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129279175..129279873 32194978 MeRIP-seq:(Medium) rs972187266 Functional Loss SNV dbSNP153 33..33 33 - - - 99677 RMVar_ID_99677 Human_SNP_ID_152970007 m1A Human chr3 - 129301994 129301994 129301994 GAGCTTCCTGAGTTGAGACTTCACCAAAGTCAAGCCATTTAGAAACTGCCTCCTCTCCATCTAAT GAGCTTCCTGAGTTGAGACTTCACCAAAGTCAGGCCATTTAGAAACTGCCTCCTCTCCATCTAAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129301951..129302025 32194978 MeRIP-seq:(Medium) rs758745235 Functional Loss SNV dbSNP153 33..33 33 - - - 99678 RMVar_ID_99678 Human_SNP_ID_152970008 m1A Human chr3 - 129301994 129301994 129301994 GAGCTTCCTGAGTTGAGACTTCACCAAAGTCAAGCCATTTAGAAACTGCCTCCTCTCCATCTAAT GAGCTTCCTGAGTTGAGACTTCACCAAAGTCACGCCATTTAGAAACTGCCTCCTCTCCATCTAAT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129301951..129302025 32194978 MeRIP-seq:(Medium) rs758745235 Functional Loss SNV dbSNP153 33..33 33 - - - 99679 RMVar_ID_99679 Human_SNP_ID_152970960 m1A Human chr3 + 129305941 129305941 129305941 CCAGGTGGGGCTCCCGCCCAGACCCTTTCCCGAGGTCCGCCCTCTCCGCCTTTTCTCTAAATTCC CCAGGTGGGGCTCCCGCCCAGACCCTTTCCCGGGGTCCGCCCTCTCCGCCTTTTCTCTAAATTCC A G HMCES Ensembl:ENSG00000183624 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129305898..129305995 26863196 MeRIP-seq:(Medium) rs1168551188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17993837 99680 RMVar_ID_99680 Human_SNP_ID_152973047 m1A Human chr3 - 129314930 129314922 129314930 CCACCGGGCGGGGTCGCTGGTTGGCCGGGCCCAGGCGCGCGGGGACGCGGAGGCCGCGCATCCTT CCACCGGGCGGGGTCGCTGGTTGGCCGGGCCC________GGGGACGCGGAGGCCGCGCATCCTT CGCGCGCCT C H1-10 Ensembl:ENSG00000184897 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:129314831..129315050 26863410 MeRIP-seq:(Medium) rs1559760361 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_589071,Human_RBP_ID_1030971,Human_RBP_ID_4722156,Human_RBP_ID_5120395,Human_RBP_ID_5150005,Human_RBP_ID_7119510,Human_RBP_ID_17661203,Human_RBP_ID_17702811,Human_RBP_ID_26510561 99681 RMVar_ID_99681 Human_SNP_ID_152973055 m1A Human chr3 - 129314930 129314930 129314930 CCACCGGGCGGGGTCGCTGGTTGGCCGGGCCCAGGCGCGCGGGGACGCGGAGGCCGCGCATCCTT CCACCGGGCGGGGTCGCTGGTTGGCCGGGCCCTGGCGCGCGGGGACGCGGAGGCCGCGCATCCTT T A H1-10 Ensembl:ENSG00000184897 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:129314831..129315050 26863410 MeRIP-seq:(Medium) rs1559760366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_589071,Human_RBP_ID_1030971,Human_RBP_ID_4722156,Human_RBP_ID_5120395,Human_RBP_ID_5150005,Human_RBP_ID_7119510,Human_RBP_ID_17661203,Human_RBP_ID_17702811,Human_RBP_ID_26510561 99682 RMVar_ID_99682 Human_SNP_ID_152973619 m1A Human chr3 - 129316064 129316064 129316064 CCCAACCCTCGCTCCGGCCCGGCCCGGCCCCCACCCCAGCCCTGCCGCCCGGCCCCAGGCCCGGC CCCAACCCTCGCTCCGGCCCGGCCCGGCCCCCCCCCCAGCCCTGCCGCCCGGCCCCAGGCCCGGC T G H1-10 Ensembl:ENSG00000184897 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:129315864..129316275 26863410 MeRIP-seq:(Medium) rs932501128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248637,Human_RBP_ID_4760914,Human_RBP_ID_5505476,Human_RBP_ID_22456170,Human_RBP_ID_22533870 99683 RMVar_ID_99683 Human_SNP_ID_152973641 m1A Human chr3 + 129316105 129316100 129316106 GGCCGGGCCGGAGCGAGGGTTGGGGGGCCCGGAGCCGGGGCCGGACTAGGGGACCGAGTTGGGGG GGCCGGGCCGGAGCGAGGGTTGGGGGGC______CCGGGGCCGGACTAGGGGACCGAGTTGGGGG CCCGGAG C H1FX-AS1 Ensembl:ENSG00000206417 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:129315801..129317205 26863196 MeRIP-seq:(Medium) rs1174022604 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_3722884,Human_RBP_ID_5208863,Human_RBP_ID_8211242,Human_RBP_ID_19116117 99684 RMVar_ID_99684 Human_SNP_ID_152973706 m1A Human chr3 + 129316204 129316204 129316204 GGGACGTAGACCTAGGCCGAGCCGGAGCGAAGAGAAATCCCGCCGAACGCGAGACACCGCCGCCG GGGACGTAGACCTAGGCCGAGCCGGAGCGAAGGGAAATCCCGCCGAACGCGAGACACCGCCGCCG A G H1FX-AS1 Ensembl:ENSG00000206417 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:129315801..129316300 26863196 MeRIP-seq:(Medium) rs1263428382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5208864,Human_RBP_ID_5605983 99685 RMVar_ID_99685 Human_SNP_ID_152973717 m1A Human chr3 + 129316227 129316227 129316227 GGAGCGAAGAGAAATCCCGCCGAACGCGAGACACCGCCGCCGCAGCTTCCACTGGCGCCTCTGGA GGAGCGAAGAGAAATCCCGCCGAACGCGAGACGCCGCCGCCGCAGCTTCCACTGGCGCCTCTGGA A G H1FX-AS1 Ensembl:ENSG00000206417 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr3:129314776..129316400;chr3:129315853..129316275 26863196 MeRIP-seq:(Medium) rs1300420109 Functional Loss SNV dbSNP153 33..33 33 - - - 99686 RMVar_ID_99686 Human_SNP_ID_152973844 m1A Human chr3 - 129316506 129316506 129316506 CACCTCTCCGTTCGCCTTTGCTGAGCCCTTCCAGGACGCAAGTCGCCTCTCCACTGCGCCGGGAG CACCTCTCCGTTCGCCTTTGCTGAGCCCTTCCGGGACGCAAGTCGCCTCTCCACTGCGCCGGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129316455..129316722 26863196 MeRIP-seq:(Medium) rs1011710577 Functional Loss SNV dbSNP153 33..33 33 - - - 99687 RMVar_ID_99687 Human_SNP_ID_152974285 m1A Human chr3 - 129318221 129318221 129318221 TTGGGTTTCCTGCTCCCATCCCATCTCTGTACACTGCGGTCACTCCAGCTGTGGCCACCATGTTC TTGGGTTTCCTGCTCCCATCCCATCTCTGTACGCTGCGGTCACTCCAGCTGTGGCCACCATGTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:129318182..129318567 26863196 MeRIP-seq:(Medium) rs1559761718 Functional Loss SNV dbSNP153 33..33 33 - - - 99688 RMVar_ID_99688 Human_SNP_ID_152991209 m1A Human chr3 - 129384768 129384766 129384768 CAGCTGTGCCTACCCAGTCGTGCCACAGACACAGGGGACCCAGAGCACCTGGTACTGCAGAGGGC CAGCTGTGCCTACCCAGTCGTGCCACAGACAC__GGGACCCAGAGCACCTGGTACTGCAGAGGGC CCT C RPL32P3 Ensembl:ENSG00000251474 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129384724..129384811 26863196 MeRIP-seq:(Medium) rs376647285 Functional Loss DEL dbSNP153 33..34 33 - - - 99689 RMVar_ID_99689 Human_SNP_ID_152995192 m1A Human chr3 + 129399359 129399356 129399360 CCTGGGAAGCAAAGTGAGACTCTGTCTCAAAAACAAACAAACAAACAAACTCACCGAGCAGGAAA CCTGGGAAGCAAAGTGAGACTCTGTCTCAA____AAACAAACAAACAAACTCACCGAGCAGGAAA AAAAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129399226..129399405 26863196 MeRIP-seq:(Medium) rs568049924 Functional Loss DEL dbSNP153 31..34 33 - - - 99690 RMVar_ID_99690 Human_SNP_ID_153003870 m1A Human chr3 + 129433965 129433965 129433965 GACCGAGGAGGTGTCCATTTCTTAAAGGCTTTACGTCGTGGGGGGCTAAGAGCTAAACAAACATA GACCGAGGAGGTGTCCATTTCTTAAAGGCTTTCCGTCGTGGGGGGCTAAGAGCTAAACAAACATA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:129433854..129434035 26863196 MeRIP-seq:(Medium) rs768532890 Functional Loss SNV dbSNP153 33..33 33 - - - 99691 RMVar_ID_99691 Human_SNP_ID_153004898 m1A Human chr3 - 129437952 129437952 129437952 AAATAAGTTAATCACTTAGACTTTGTTTTTCCAGCAAAGAAGATGTTGCTATGGAATTGGAAAGA AAATAAGTTAATCACTTAGACTTTGTTTTTCCGGCAAAGAAGATGTTGCTATGGAATTGGAAAGA T C MBD4 Ensembl:ENSG00000129071 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129437906..129439982 26863196 MeRIP-seq:(Medium) rs1377666890 Functional Loss SNV dbSNP153 33..33 33 - - - 99692 RMVar_ID_99692 Human_SNP_ID_153005587 m1A Human chr3 - 129440344 129440344 129440344 CTCACCAGTGCTCGGCTTTATCTCTCCACGTCAACACGGCCCTCATCACGGCTTCCCTTACGGCT CTCACCAGTGCTCGGCTTTATCTCTCCACGTCCACACGGCCCTCATCACGGCTTCCCTTACGGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129440214..129449933 26863196 MeRIP-seq:(Medium) rs1472417931 Functional Loss SNV dbSNP153 33..33 33 - - - 99693 RMVar_ID_99693 Human_SNP_ID_153005589 m1A Human chr3 + 129440352 129440352 129440352 GGGAAGCCGTGATGAGGGCCGTGTTGACGTGGAGAGATAAAGCCGAGCACTGGTGAGGAGCGGGG GGGAAGCCGTGATGAGGGCCGTGTTGACGTGGGGAGATAAAGCCGAGCACTGGTGAGGAGCGGGG A G IFT122 Ensembl:ENSG00000163913 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129440215..129440399 26863196 MeRIP-seq:(Medium) rs1228704098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_480943,Human_Splice_Rec_481003,Human_Splice_Rec_481057,Human_Splice_Rec_481113,Human_Splice_Rec_481173,Human_Splice_Rec_481231,Human_Splice_Rec_481289,Human_Splice_Rec_481349,Human_Splice_Rec_481397 99694 RMVar_ID_99694 Human_SNP_ID_153024189 m1A Human chr3 - 129514505 129514505 129514505 GCTTGGCGCGGATGGTCAGGGTACCCAGCTCAATGGACTTTTGGAATCTGGCAGGGATGTACAGG GCTTGGCGCGGATGGTCAGGGTACCCAGCTCAGTGGACTTTTGGAATCTGGCAGGGATGTACAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:129514454..129514655 32194978 MeRIP-seq:(Medium) rs759062038 Functional Loss SNV dbSNP153 33..33 33 - - - 99695 RMVar_ID_99695 Human_SNP_ID_153039846 m1A Human chr3 - 129567726 129567726 129567726 CAGAAGACGCTGCTGCAGATGGAGGAGATGGAATCTCAGATCCGAGAGGAAATCCGCAAAGGTAG CAGAAGACGCTGCTGCAGATGGAGGAGATGGAGTCTCAGATCCGAGAGGAAATCCGCAAAGGTAG T C PLXND1 Ensembl:ENSG00000004399 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129566571..129567725 32194978 MeRIP-seq:(Medium) rs369857384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19013003 Human_Splice_Rec_481734,Human_Splice_Rec_481735 Human_miRNA_ID_2403231 RMVar_hsa_circ_98581,RMVar_hsa_circ_93019,RMVar_hsa_circ_83585,RMVar_hsa_circ_221170,RMVar_hsa_circ_221172,RMVar_hsa_circ_13464,RMVar_hsa_circ_104540,RMVar_hsa_circ_221176,RMVar_hsa_circ_120545,RMVar_hsa_circ_221178,RMVar_hsa_circ_340795,RMVar_hsa_circ_83809,RMVar_hsa_circ_221179,RMVar_hsa_circ_221180 99696 RMVar_ID_99696 Human_SNP_ID_153040821 m1A Human chr3 - 129571232 129571232 129571232 TCCCCCGGGGCCCTGAGCAACGCATCAGCGCCAGTGGACTTCTTCATCAATGGGCGGGCCTACGC TCCCCCGGGGCCCTGAGCAACGCATCAGCGCCGGTGGACTTCTTCATCAATGGGCGGGCCTACGC T C PLXND1 Ensembl:ENSG00000004399 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:129571185..129571768 32194978 MeRIP-seq:(Medium) rs976527871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_481728,Human_Splice_Rec_481834,Human_Splice_Rec_481840 Human_miRNA_ID_2967780 RMVar_hsa_circ_98581,RMVar_hsa_circ_93019,RMVar_hsa_circ_83585,RMVar_hsa_circ_221170,RMVar_hsa_circ_221172,RMVar_hsa_circ_13464,RMVar_hsa_circ_104540,RMVar_hsa_circ_221176,RMVar_hsa_circ_120545,RMVar_hsa_circ_221178,RMVar_hsa_circ_83809,RMVar_hsa_circ_91378,RMVar_hsa_circ_221179,RMVar_hsa_circ_221180,RMVar_hsa_circ_221181,RMVar_hsa_circ_39098,RMVar_hsa_circ_378558 99697 RMVar_ID_99697 Human_SNP_ID_153041150 m1A Human chr3 - 129572003 129572003 129572003 TGGGATGGGGCGGAATTTGGAAGTGTAAGGAAACAGCTGGGCACTAACTGGGCAGAAGATGAGTT TGGGATGGGGCGGAATTTGGAAGTGTAAGGAAGCAGCTGGGCACTAACTGGGCAGAAGATGAGTT T C PLXND1 Ensembl:ENSG00000004399 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:129571952..129572153 26863196 MeRIP-seq:(Medium) rs1049093906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98581,RMVar_hsa_circ_93019,RMVar_hsa_circ_83585,RMVar_hsa_circ_221170,RMVar_hsa_circ_221172,RMVar_hsa_circ_13464,RMVar_hsa_circ_104540,RMVar_hsa_circ_221176,RMVar_hsa_circ_120545,RMVar_hsa_circ_221178,RMVar_hsa_circ_83809,RMVar_hsa_circ_91378,RMVar_hsa_circ_221179,RMVar_hsa_circ_221180,RMVar_hsa_circ_221181,RMVar_hsa_circ_378558,RMVar_hsa_circ_221182,RMVar_hsa_circ_77633,RMVar_hsa_circ_127972,RMVar_hsa_circ_221183 99698 RMVar_ID_99698 Human_SNP_ID_153046747 m1A Human chr3 - 129592081 129592081 129592081 GGGTGGGGGGGAATGGCTTCCTGGGCAGAGGGAGCGGCCAGGCCAGAGGTCCTGAGGCAGGAACG GGGTGGGGGGGAATGGCTTCCTGGGCAGAGGGGGCGGCCAGGCCAGAGGTCCTGAGGCAGGAACG T C PLXND1 Ensembl:ENSG00000004399 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129592045..129592123 26863196 MeRIP-seq:(Medium) rs952917209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120545,RMVar_hsa_circ_221179 99699 RMVar_ID_99699 Human_SNP_ID_153048439 m1A Human chr3 - 129598193 129598193 129598193 GGCATTCCAGGCAGAGCACACGATAGGGGCAAAGGCTCAGAGATGTTGGAATGTGGCTTGGGTAG GGCATTCCAGGCAGAGCACACGATAGGGGCAAGGGCTCAGAGATGTTGGAATGTGGCTTGGGTAG T C PLXND1 Ensembl:ENSG00000004399 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129598187..129598273 26863196 MeRIP-seq:(Medium) rs1417537741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120545,RMVar_hsa_circ_221179 99700 RMVar_ID_99700 Human_SNP_ID_153050169 m1A Human chr3 + 129605314 129605296 129605314 CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGGGTGTACCTGGATGTTGAGCTTGCG CCCCCGCCGCCGCCG__________________CCGCCCGGGTGTACCTGGATGTTGAGCTTGCG GCCGCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:129605181..129605396;chr3:129605180..129605397 26863196 MeRIP-seq:(Medium) rs1313470438 Functional Loss DEL dbSNP153 16..33 33 - - - 99701 RMVar_ID_99701 Human_SNP_ID_153050178 m1A Human chr3 + 129605314 129605305 129605314 CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGGGTGTACCTGGATGTTGAGCTTGCG CCCCCGCCGCCGCCGCCGCCGCCG_________CCGCCCGGGTGTACCTGGATGTTGAGCTTGCG GCCGCCGCCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:129605181..129605396;chr3:129605180..129605397 26863196 MeRIP-seq:(Medium) rs1351785066 Functional Loss DEL dbSNP153 25..33 33 - - - 99702 RMVar_ID_99702 Human_SNP_ID_153050188 m1A Human chr3 + 129605314 129605314 129605314 CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGGGTGTACCTGGATGTTGAGCTTGCG CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCCGGGTGTACCTGGATGTTGAGCTTGCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:129605181..129605396;chr3:129605180..129605397 26863196 MeRIP-seq:(Medium) rs1411597579 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 99703 RMVar_ID_99703 Human_SNP_ID_153050189 m1A Human chr3 + 129605314 129605314 129605314 CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGGGTGTACCTGGATGTTGAGCTTGCG CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGGGTGTACCTGGATGTTGAGCTTGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:129605181..129605396;chr3:129605180..129605397 26863196 MeRIP-seq:(Medium) rs1411597579 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 99704 RMVar_ID_99704 Human_SNP_ID_153050480 m1A Human chr3 - 129605873 129605873 129605873 GCGCGGCGACCTGGCCAAGCTCTTCACCTTCGACCTCAACCCCTCCGACGACAACATCCTCAAGA GCGCGGCGACCTGGCCAAGCTCTTCACCTTCGGCCTCAACCCCTCCGACGACAACATCCTCAAGA T C PLXND1 Ensembl:ENSG00000004399 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:129605823..129605944 26863196 MeRIP-seq:(Medium) rs749979407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18194720,Human_RBP_ID_27498043 Human_miRNA_ID_2152930,Human_miRNA_ID_2800806,Human_miRNA_ID_3008935 RMVar_hsa_circ_120545,RMVar_hsa_circ_221179 99705 RMVar_ID_99705 Human_SNP_ID_153050711 m1A Human chr3 + 129606500 129606500 129606500 GCGTGGGCGAGGGGAACCGACGCTGGATCTCCAGGGCGCCGGCCCGCGCCGCCCCCAGGAGCAGC GCGTGGGCGAGGGGAACCGACGCTGGATCTCCTGGGCGCCGGCCCGCGCCGCCCCCAGGAGCAGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:129606450..129606701 26863196 MeRIP-seq:(Medium) rs775527662 Functional Loss SNV dbSNP153 33..33 33 - - - 99706 RMVar_ID_99706 Human_SNP_ID_153056424 m1A Human chr3 - 129627673 129627673 129627673 CCCTCCAGCCACTGGCCTCAAAACCACCGAGCACATCCACGCGGCCCTCGCCGACTCCCGCAGGG CCCTCCAGCCACTGGCCTCAAAACCACCGAGCGCATCCACGCGGCCCTCGCCGACTCCCGCAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129627625..129627838 26863196 MeRIP-seq:(Medium) rs575632804 Functional Loss SNV dbSNP153 33..33 33 - - - 99707 RMVar_ID_99707 Human_SNP_ID_153118759 m1A Human chr3 + 129893661 129893637 129893661 CCGCCTCAGCCGCCGCCGCCTCAGTCACCGCCACCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG CCGCCTCAG________________________CCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG GCCGCCGCCGCCTCAGTCACCGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129893632..129893706 26863196 MeRIP-seq:(Medium) rs1309972235 Functional Loss DEL dbSNP153 10..33 33 - - - 99708 RMVar_ID_99708 Human_SNP_ID_153118762 m1A Human chr3 + 129893661 129893640 129893661 CCGCCTCAGCCGCCGCCGCCTCAGTCACCGCCACCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG CCGCCTCAGCCG_____________________CCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG GCCGCCGCCTCAGTCACCGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129893632..129893706 26863196 MeRIP-seq:(Medium) rs1457732857 Functional Loss DEL dbSNP153 13..33 33 - - - 99709 RMVar_ID_99709 Human_SNP_ID_153118769 m1A Human chr3 + 129893661 129893661 129893661 CCGCCTCAGCCGCCGCCGCCTCAGTCACCGCCACCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG CCGCCTCAGCCGCCGCCGCCTCAGTCACCGCCGCCGCCGCCGCCGCCTCAGCCCCGGCGCGGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129893632..129893706 26863196 MeRIP-seq:(Medium) rs912383977 Functional Loss SNV dbSNP153 33..33 33 - - - 99710 RMVar_ID_99710 Human_SNP_ID_153118792 m1A Human chr3 + 129893698 129893698 129893698 CGCCGCCGCCTCAGCCCCGGCGCGGGAGGGCGAACCGGCGCGAGAGAGCGAGCGCGCGCGCGCCC CGCCGCCGCCTCAGCCCCGGCGCGGGAGGGCGGACCGGCGCGAGAGAGCGAGCGCGCGCGCGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:129893655..129893743 26863196 MeRIP-seq:(Medium) rs935553699 Functional Loss SNV dbSNP153 33..33 33 - - - 99711 RMVar_ID_99711 Human_SNP_ID_153335633 m1A Human chr3 + 130746630 130746630 130746630 GACCCCTCCAGCCCCCTAACCTGCCCTGGGGGACATGCGTTCCCGGGCCTCGTCTTCCTCTAGCG GACCCCTCCAGCCCCCTAACCTGCCCTGGGGGCCATGCGTTCCCGGGCCTCGTCTTCCTCTAGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:130746579..130746786 26863196 MeRIP-seq:(Medium) rs2293179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5505511,Human_RBP_ID_7243171 GWAS_ID_13145,GWAS_ID_13146 99712 RMVar_ID_99712 Human_SNP_ID_153370594 m1A Human chr3 + 130894052 130894052 130894052 TGCGGGGCGCGACTGGGCGGCCGGCGGCGGGGAGGGGCGGAGCGCAGGAGTCGGAGGCGGGAGCA TGCGGGGCGCGACTGGGCGGCCGGCGGCGGGGGGGGGCGGAGCGCAGGAGTCGGAGGCGGGAGCA A G ATP2C1 Ensembl:ENSG00000017260 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:130894007..130894132;chr3:130894006..130894124 26863196 MeRIP-seq:(Medium) rs959162123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835133,Human_RBP_ID_4756732 99713 RMVar_ID_99713 Human_SNP_ID_153370695 m1A Human chr3 - 130894251 130894251 130894251 CGGGGGCGCCCCGCGCGCCTCGGGAGAAGAGGAGCTGCTCGCGGGGCAGCGGTGCGAGGCGGGAG CGGGGGCGCCCCGCGCGCCTCGGGAGAAGAGGTGCTGCTCGCGGGGCAGCGGTGCGAGGCGGGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:130894201..130894280 26863196 MeRIP-seq:(Medium) rs929821101 Functional Loss SNV dbSNP153 33..33 33 - - - 99714 RMVar_ID_99714 Human_SNP_ID_153370696 m1A Human chr3 - 130894251 130894251 130894251 CGGGGGCGCCCCGCGCGCCTCGGGAGAAGAGGAGCTGCTCGCGGGGCAGCGGTGCGAGGCGGGAG CGGGGGCGCCCCGCGCGCCTCGGGAGAAGAGGGGCTGCTCGCGGGGCAGCGGTGCGAGGCGGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:130894201..130894280 26863196 MeRIP-seq:(Medium) rs929821101 Functional Loss SNV dbSNP153 33..33 33 - - - 99715 RMVar_ID_99715 Human_SNP_ID_153370823 m1A Human chr3 - 130894659 130894659 130894659 GAGGAGGAGGACAAGGAAGAGAAGCCCCCGGAATCCCAGGCTGTCACCCCCGCTCCCGGCCACGC GAGGAGGAGGACAAGGAAGAGAAGCCCCCGGAGTCCCAGGCTGTCACCCCCGCTCCCGGCCACGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:130894572..130894697 26863196 MeRIP-seq:(Medium) rs1362987732 Functional Loss SNV dbSNP153 33..33 33 - - - 99716 RMVar_ID_99716 Human_SNP_ID_153376791 m1A Human chr3 - 130919277 130919277 130919277 GAGGTTGTAGTAAGCTGAGATCGCGCCATTGCACTCTAGCCTCGGCGAAAAGAGCAAAACTCTCT GAGGTTGTAGTAAGCTGAGATCGCGCCATTGCCCTCTAGCCTCGGCGAAAAGAGCAAAACTCTCT T G AC055733.2 Ensembl:ENSG00000250592 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:130919265..130919392 26863196 MeRIP-seq:(Medium) rs543495077 Functional Loss SNV dbSNP153 33..33 33 - - - 99717 RMVar_ID_99717 Human_SNP_ID_153402134 m1A Human chr3 - 131026688 131026688 131026688 CCCTCTTTAGCTACTTAGCGCCTCTGGGCCCGAGAACACCTGCTCCTTGGCTCAGTCTGGCGCCA CCCTCTTTAGCTACTTAGCGCCTCTGGGCCCGCGAACACCTGCTCCTTGGCTCAGTCTGGCGCCA T G ASTE1 Ensembl:ENSG00000034533 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:131026637..131026773 26863196 MeRIP-seq:(Medium) rs1333321590 Functional Loss SNV dbSNP153 33..33 33 - - - 99718 RMVar_ID_99718 Human_SNP_ID_153483793 m1A Human chr3 + 131381377 131381377 131381377 AGGTTCAGGGCGCTGCCACATCTTCAGCCCCGACCCGCCGCAAGTCTCATTTCCTCCTAACCCCA AGGTTCAGGGCGCTGCCACATCTTCAGCCCCGCCCCGCCGCAAGTCTCATTTCCTCCTAACCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:131381332..131381442 26863196 MeRIP-seq:(Medium) rs929398179 Functional Loss SNV dbSNP153 33..33 33 - - - 99719 RMVar_ID_99719 Human_SNP_ID_153484773 m1A Human chr3 + 131384408 131384408 131384408 TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGAAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGCAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC A C NUDT16 Ensembl:ENSG00000198585 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:131384365..131384643 26863196 MeRIP-seq:(Medium) rs1023234810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2748487,Human_RBP_ID_7121014,Human_RBP_ID_23969566 99720 RMVar_ID_99720 Human_SNP_ID_153484774 m1A Human chr3 + 131384408 131384408 131384408 TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGAAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGGAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC A G NUDT16 Ensembl:ENSG00000198585 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:131384365..131384643 26863196 MeRIP-seq:(Medium) rs1023234810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2748487,Human_RBP_ID_7121014,Human_RBP_ID_23969566 99721 RMVar_ID_99721 Human_SNP_ID_153484775 m1A Human chr3 + 131384408 131384408 131384408 TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGAAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC TGGAAGGCAGGCTGTACTGGTTGAGTGAATGGTAAGTTGGGGAGTAGAACGTGTGAGAAGTTGGC A T NUDT16 Ensembl:ENSG00000198585 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:131384365..131384643 26863196 MeRIP-seq:(Medium) rs1023234810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2748487,Human_RBP_ID_7121014,Human_RBP_ID_23969566 99722 RMVar_ID_99722 Human_SNP_ID_153502784 m1A Human chr3 + 131462428 131462423 131462428 TTAATAAAAGTTAAATTTACAGACATCTTAAGATAACTTGGGAAATATGTAGTAAAAAAGAATCG TTAATAAAAGTTAAATTTACAGACATCT_____TAACTTGGGAAATATGTAGTAAAAAAGAATCG TTAAGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:131462359..131462459 32194978 MeRIP-seq:(Medium) rs567308599 Functional Loss DEL dbSNP153 29..33 33 - - - 99723 RMVar_ID_99723 Human_SNP_ID_153502785 m1A Human chr3 + 131462428 131462428 131462428 TTAATAAAAGTTAAATTTACAGACATCTTAAGATAACTTGGGAAATATGTAGTAAAAAAGAATCG TTAATAAAAGTTAAATTTACAGACATCTTAAGGTAACTTGGGAAATATGTAGTAAAAAAGAATCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:131462359..131462459 32194978 MeRIP-seq:(Medium) rs1222240219 Functional Loss SNV dbSNP153 33..33 33 - - - 99724 RMVar_ID_99724 Human_SNP_ID_153502822 m1A Human chr3 - 131462626 131462626 131462626 ACCACCAGAAATCATACTCTCCTTTCTTAGTCACAACAAAATCACACATGTCATCTTTGTCAAGG ACCACCAGAAATCATACTCTCCTTTCTTAGTCTCAACAAAATCACACATGTCATCTTTGTCAAGG T A MRPL3 Ensembl:ENSG00000114686 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs892986016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3686323,Human_RBP_ID_7121201,Human_RBP_ID_14622890,Human_RBP_ID_17288248,Human_RBP_ID_17401659,Human_RBP_ID_17517122,Human_RBP_ID_17994156,Human_RBP_ID_23969633,Human_RBP_ID_26824129 Human_miRNA_ID_251739 RMVar_hsa_circ_221294 99725 RMVar_ID_99725 Human_SNP_ID_153502823 m1A Human chr3 - 131462626 131462626 131462626 ACCACCAGAAATCATACTCTCCTTTCTTAGTCACAACAAAATCACACATGTCATCTTTGTCAAGG ACCACCAGAAATCATACTCTCCTTTCTTAGTCGCAACAAAATCACACATGTCATCTTTGTCAAGG T C MRPL3 Ensembl:ENSG00000114686 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs892986016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3686323,Human_RBP_ID_7121201,Human_RBP_ID_14622890,Human_RBP_ID_17288248,Human_RBP_ID_17401659,Human_RBP_ID_17517122,Human_RBP_ID_17994156,Human_RBP_ID_23969633,Human_RBP_ID_26824129 Human_miRNA_ID_251739 RMVar_hsa_circ_221294 99726 RMVar_ID_99726 Human_SNP_ID_153506415 m1A Human chr3 - 131477333 131477333 131477333 AGACGAGGAGGGATATGAAGGGAAAAGAAGGTAGGAGAATCCAGTGGCTTCTCAAGGGAGATACT AGACGAGGAGGGATATGAAGGGAAAAGAAGGTGGGAGAATCCAGTGGCTTCTCAAGGGAGATACT T C MRPL3 Ensembl:ENSG00000114686 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:131477294..131477363 26863196 MeRIP-seq:(Medium) rs1180215597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7121370 RMVar_hsa_circ_45611,RMVar_hsa_circ_62954,RMVar_hsa_circ_347162 99727 RMVar_ID_99727 Human_SNP_ID_153512957 m1A Human chr3 + 131502813 131502813 131502813 ACCTGGGCGCCGACCTGCGTCAGCAGCCTCCAACCCGGCATGGATTAGCCCGGGAAGACTCGACT ACCTGGGCGCCGACCTGCGTCAGCAGCCTCCACCCCGGCATGGATTAGCCCGGGAAGACTCGACT A C AC107027.1 Ensembl:ENSG00000248468 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:131502735..131502975 26863196 MeRIP-seq:(Medium) rs1391856968 Functional Loss SNV dbSNP153 33..33 33 - - - 99728 RMVar_ID_99728 Human_SNP_ID_153513026 m1A Human chr3 + 131502914 131502914 131502914 GAGTCCCCACGCCACCGCCACGTGGACGCAGTAGCCGTGGGGAAGTTTTCGCAATGGCCGCCGGA GAGTCCCCACGCCACCGCCACGTGGACGCAGTGGCCGTGGGGAAGTTTTCGCAATGGCCGCCGGA A G AC107027.1 Ensembl:ENSG00000248468 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:131502673..131502975 26863196 MeRIP-seq:(Medium) rs1233674449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_483955,Human_Splice_Rec_483965 99729 RMVar_ID_99729 Human_SNP_ID_153733790 m1A Human chr3 + 132417573 132417573 132417573 TCCAGAGTGAAACTCTGAGAGGCAGAGGGAGGAGGCGGAGGGGGCGGGGAGGCAGCGCCGCGGCG TCCAGAGTGAAACTCTGAGAGGCAGAGGGAGGCGGCGGAGGGGGCGGGGAGGCAGCGCCGCGGCG A C DNAJC13 Ensembl:ENSG00000138246 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr3:132417526..132417725;chr3:132417525..132417658;chr3:132417525..132434602 26863196 MeRIP-seq:(Medium) rs1212399130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756740,Human_RBP_ID_8236092,Human_RBP_ID_24553981 99730 RMVar_ID_99730 Human_SNP_ID_153737978 m1A Human chr3 + 132434488 132434488 132434488 CTTGCTACCTTTCTTAGGGGAATCTTGGAAAGATTAAAGATATATAACATGTACTAAGTGCCCTC CTTGCTACCTTTCTTAGGGGAATCTTGGAAAGGTTAAAGATATATAACATGTACTAAGTGCCCTC A G DNAJC13 Ensembl:ENSG00000138246 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:132434485..132434561 26863196 MeRIP-seq:(Medium) rs900593346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107436,RMVar_hsa_circ_112750,RMVar_hsa_circ_221305,RMVar_hsa_circ_221306 99731 RMVar_ID_99731 Human_SNP_ID_153791143 m1A Human chr3 - 132660560 132660560 132660560 GTTCCCGCTCCAGCTCCTGGACCCGCTGCTGCAGGCGCTCCACAGACTCCGCCATGGCTGGGACT GTTCCCGCTCCAGCTCCTGGACCCGCTGCTGCGGGCGCTCCACAGACTCCGCCATGGCTGGGACT T C NPHP3-ACAD11 Ensembl:ENSG00000274810 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:132660351..132660709 26863196 MeRIP-seq:(Medium) rs1004184496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784949 99732 RMVar_ID_99732 Human_SNP_ID_153792223 m1A Human chr3 + 132665803 132665803 132665803 ACTAATACCTAAAAGACTGTAAGCTTTAAAACATATTTTTCTTTGTTTTAAGCCGCTTGATGGCA ACTAATACCTAAAAGACTGTAAGCTTTAAAACGTATTTTTCTTTGTTTTAAGCCGCTTGATGGCA A G UBA5 Ensembl:ENSG00000081307 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:132665801..132665875 26863196 MeRIP-seq:(Medium) rs781682144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1309865,Human_RBP_ID_1949415,Human_RBP_ID_2748835,Human_RBP_ID_14625712,Human_RBP_ID_18169647,Human_RBP_ID_25766491 Human_Splice_Rec_484935,Human_Splice_Rec_484957,Human_Splice_Rec_484981,Human_Splice_Rec_485007,Human_Splice_Rec_485013,Human_Splice_Rec_485017,Human_Splice_Rec_485037,Human_Splice_Rec_485071 99733 RMVar_ID_99733 Human_SNP_ID_153792224 m1A Human chr3 + 132665803 132665803 132665803 ACTAATACCTAAAAGACTGTAAGCTTTAAAACATATTTTTCTTTGTTTTAAGCCGCTTGATGGCA ACTAATACCTAAAAGACTGTAAGCTTTAAAACTTATTTTTCTTTGTTTTAAGCCGCTTGATGGCA A T UBA5 Ensembl:ENSG00000081307 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:132665801..132665875 26863196 MeRIP-seq:(Medium) rs781682144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1309865,Human_RBP_ID_1949415,Human_RBP_ID_2748835,Human_RBP_ID_14625712,Human_RBP_ID_18169647,Human_RBP_ID_25766491 Human_Splice_Rec_484935,Human_Splice_Rec_484957,Human_Splice_Rec_484981,Human_Splice_Rec_485007,Human_Splice_Rec_485013,Human_Splice_Rec_485017,Human_Splice_Rec_485037,Human_Splice_Rec_485071 99734 RMVar_ID_99734 Human_SNP_ID_153805971 m1A Human chr3 - 132722252 132722252 132722252 CGGCGAGGCCTGCGAGATCCCGGTGGAGGTGAAGCCCAAGGCCCGCCTGCTGCGCAACTCGTTCC CGGCGAGGCCTGCGAGATCCCGGTGGAGGTGAGGCCCAAGGCCCGCCTGCTGCGCAACTCGTTCC T C NPHP3-ACAD11,NPHP3 Ensembl:ENSG00000274810,Ensembl:ENSG00000113971 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:132722131..132722347 26863196 MeRIP-seq:(Medium) rs572295745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19013034,Human_RBP_ID_22093135,Human_RBP_ID_27822492 99735 RMVar_ID_99735 Human_SNP_ID_153806017 m1A Human chr3 - 132722349 132722349 132722349 ACTAGGTAGTAGCGGCAACGGACGCCATGGGGACCGCCTCGTCGCTCGTGAGCCCCGCGGGCGGG ACTAGGTAGTAGCGGCAACGGACGCCATGGGGTCCGCCTCGTCGCTCGTGAGCCCCGCGGGCGGG T A NPHP3-ACAD11,NPHP3 Ensembl:ENSG00000274810,Ensembl:ENSG00000113971 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:132722146..132722351 26863196 MeRIP-seq:(Medium) rs750123809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_485219 99736 RMVar_ID_99736 Human_SNP_ID_153806018 m1A Human chr3 - 132722349 132722349 132722349 ACTAGGTAGTAGCGGCAACGGACGCCATGGGGACCGCCTCGTCGCTCGTGAGCCCCGCGGGCGGG ACTAGGTAGTAGCGGCAACGGACGCCATGGGGGCCGCCTCGTCGCTCGTGAGCCCCGCGGGCGGG T C NPHP3-ACAD11,NPHP3 Ensembl:ENSG00000274810,Ensembl:ENSG00000113971 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:132722146..132722351 26863196 MeRIP-seq:(Medium) rs750123809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_485219 99737 RMVar_ID_99737 Human_SNP_ID_154011925 m1A Human chr3 + 133573814 133573814 133573814 TCCGCCGTCGCAGCAGCAGCGGCAGCCCCGGCAGCCTCGGGCGACAGCGGCGGCGCGCGAGCCCC TCCGCCGTCGCAGCAGCAGCGGCAGCCCCGGCGGCCTCGGGCGACAGCGGCGGCGCGCGAGCCCC A G CDV3 Ensembl:ENSG00000091527 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:133573651..133574325 26863410 MeRIP-seq:(Medium) rs1215374515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835676,Human_RBP_ID_4757459 RMVar_hsa_circ_113168,RMVar_hsa_circ_221402 99738 RMVar_ID_99738 Human_SNP_ID_154012039 m1A Human chr3 - 133574050 133574050 133574050 AAGAAGTTGTCCAGGCTCCGCTCCTCCGTCTCAGCCATGGCCTCGGCCTCCTCGACCCGGATGGG AAGAAGTTGTCCAGGCTCCGCTCCTCCGTCTCGGCCATGGCCTCGGCCTCCTCGACCCGGATGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:133573970..133574064 26863410 MeRIP-seq:(Medium) rs1195429336 Functional Loss SNV dbSNP153 33..33 33 - - - 99739 RMVar_ID_99739 Human_SNP_ID_154012052 m1A Human chr3 - 133574083 133574083 133574083 CGCTCCTTCTTCTTCTTCTTGTCCCTCTTGGCAAAGAAGTTGTCCAGGCTCCGCTCCTCCGTCTC CGCTCCTTCTTCTTCTTCTTGTCCCTCTTGGCGAAGAAGTTGTCCAGGCTCCGCTCCTCCGTCTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:133573701..133574125 26863196 MeRIP-seq:(Medium) rs1273748782 Functional Loss SNV dbSNP153 33..33 33 - - - 99740 RMVar_ID_99740 Human_SNP_ID_154012079 m1A Human chr3 + 133574173 133574134 133574173 GGCGCAGCGGGCAGCGCCGGCGGAAGCAGTGGAGCCGCGGGTGCGGCGGGCGGCGGGGCGGGCGC _________________________________GCCGCGGGTGCGGCGGGCGGCGGGGCGGGCGC TGCCGCGGGCGCAGCGGGCAGCGCCGGCGGAAGCAGTGGA T CDV3 Ensembl:ENSG00000091527 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:133574101..133574224 26863196 MeRIP-seq:(Medium) rs1426206205 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_835285,Human_RBP_ID_9354422,Human_RBP_ID_9395521 Human_Splice_Rec_485485 Human_miRNA_ID_2967787 RMVar_hsa_circ_113168,RMVar_hsa_circ_221402 99741 RMVar_ID_99741 Human_SNP_ID_154012080 m1A Human chr3 + 133574146 133574137 133574146 CGGAGCAACCGGGCGGCGAGTGCCGCGGGCGCAGCGGGCAGCGCCGGCGGAAGCAGTGGAGCCGC CGGAGCAACCGGGCGGCGAGTGCC_________GCGGGCAGCGCCGGCGGAAGCAGTGGAGCCGC CGCGGGCGCA C CDV3 Ensembl:ENSG00000091527 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:133573677..133574474 26863196 MeRIP-seq:(Medium) rs750691426 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_212740,Human_RBP_ID_247115,Human_RBP_ID_937218,Human_RBP_ID_1633028,Human_RBP_ID_9394097,Human_RBP_ID_26347213 Human_Splice_Rec_485485 RMVar_hsa_circ_113168,RMVar_hsa_circ_221402 99742 RMVar_ID_99742 Human_SNP_ID_154012464 m1A Human chr3 - 133575028 133575028 133575028 ATTCTTTCCATTCATCTTCGTCCTGTAAAACAAACGCCATTTGATCAATTAAAGCTATTTGTAGA ATTCTTTCCATTCATCTTCGTCCTGTAAAACAGACGCCATTTGATCAATTAAAGCTATTTGTAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:133575026..133575075 26863196 MeRIP-seq:(Medium) rs1424251742 Functional Loss SNV dbSNP153 33..33 33 - - - 99743 RMVar_ID_99743 Human_SNP_ID_154012687 m1A Human chr3 - 133575830 133575830 133575830 CCAAAATATAGCACTTACTTAACATCAACCTTAAAGTTGACTGCCATAGACTGGACTTGACAAAA CCAAAATATAGCACTTACTTAACATCAACCTTGAAGTTGACTGCCATAGACTGGACTTGACAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:133575026..133586643 26863196 MeRIP-seq:(Medium) rs1367962651 Functional Loss SNV dbSNP153 33..33 33 - - - 99744 RMVar_ID_99744 Human_SNP_ID_154015650 m1A Human chr3 - 133586536 133586536 133586536 CTGTAACTAATATTTTATAACAATTTTTAGATAAACTATTTAAATGCTCAGCATTTTAATAAGCT CTGTAACTAATATTTTATAACAATTTTTAGATTAACTATTTAAATGCTCAGCATTTTAATAAGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:133586533..133586643 26863196 MeRIP-seq:(Medium) rs199960057 Functional Loss SNV dbSNP153 33..33 33 - - - 99745 RMVar_ID_99745 Human_SNP_ID_154015651 m1A Human chr3 - 133586536 133586536 133586536 CTGTAACTAATATTTTATAACAATTTTTAGATAAACTATTTAAATGCTCAGCATTTTAATAAGCT CTGTAACTAATATTTTATAACAATTTTTAGATGAACTATTTAAATGCTCAGCATTTTAATAAGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:133586533..133586643 26863196 MeRIP-seq:(Medium) rs199960057 Functional Loss SNV dbSNP153 33..33 33 - - - 99746 RMVar_ID_99746 Human_SNP_ID_154015652 m1A Human chr3 - 133586536 133586536 133586536 CTGTAACTAATATTTTATAACAATTTTTAGATAAACTATTTAAATGCTCAGCATTTTAATAAGCT CTGTAACTAATATTTTATAACAATTTTTAGATCAACTATTTAAATGCTCAGCATTTTAATAAGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:133586533..133586643 26863196 MeRIP-seq:(Medium) rs199960057 Functional Loss SNV dbSNP153 33..33 33 - - - 99747 RMVar_ID_99747 Human_SNP_ID_154016113 m1A Human chr3 + 133588092 133588092 133588092 CTAACCCTTCTGAGGTAACTAGACTGCAGCTAACCACCACCAACAGCCATTCATCATCTGATCTC CTAACCCTTCTGAGGTAACTAGACTGCAGCTACCCACCACCAACAGCCATTCATCATCTGATCTC A C CDV3 Ensembl:ENSG00000091527 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:133588043..133588155 26863196 MeRIP-seq:(Medium) rs1298523338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_589661,Human_RBP_ID_1309899,Human_RBP_ID_1618061,Human_RBP_ID_1949503,Human_RBP_ID_3686697,Human_RBP_ID_7122537,Human_RBP_ID_8867911,Human_RBP_ID_14627141,Human_RBP_ID_17288268,Human_RBP_ID_17401679,Human_RBP_ID_17517155,Human_RBP_ID_17994355,Human_RBP_ID_26824135,Human_RBP_ID_27313476,Human_RBP_ID_27498223,Human_RBP_ID_27565748 RMVar_hsa_circ_113168,RMVar_hsa_circ_221402 99748 RMVar_ID_99748 Human_SNP_ID_154023463 m1A Human chr3 - 133617163 133617163 133617163 GCCAACCCCCCTGTGGCTCCGCACCCTAGAGAAAAGGTTTGTTGATCCTTAATATGGTGATACAG GCCAACCCCCCTGTGGCTCCGCACCCTAGAGAGAAGGTTTGTTGATCCTTAATATGGTGATACAG T C TOPBP1 Ensembl:ENSG00000163781 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:133617151..133617269 26863196 MeRIP-seq:(Medium) rs781205194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1618159,Human_RBP_ID_3686767,Human_RBP_ID_23027089,Human_RBP_ID_25766519 Human_Splice_Rec_485583,Human_Splice_Rec_485637,Human_Splice_Rec_485649 RMVar_hsa_circ_55116,RMVar_hsa_circ_310421,RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_313001,RMVar_hsa_circ_7996,RMVar_hsa_circ_48052,RMVar_hsa_circ_221407,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221413,RMVar_hsa_circ_221411,RMVar_hsa_circ_11778,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_275051,RMVar_hsa_circ_301277,RMVar_hsa_circ_63543,RMVar_hsa_circ_334429,RMVar_hsa_circ_356538,RMVar_hsa_circ_221410,RMVar_hsa_circ_376382,RMVar_hsa_circ_345819,RMVar_hsa_circ_272456,RMVar_hsa_circ_50715,RMVar_hsa_circ_118952,RMVar_hsa_circ_221412,RMVar_hsa_circ_94542,RMVar_hsa_circ_221414,RMVar_hsa_circ_221415 99749 RMVar_ID_99749 Human_SNP_ID_154033515 m1A Human chr3 - 133659472 133659472 133659472 GAGAAGTAGGAGGTAAAGGTGGAAAGATAGGCAGGAAACCAGACTGTGTTGTCTTGAAGGCTGTA GAGAAGTAGGAGGTAAAGGTGGAAAGATAGGCGGGAAACCAGACTGTGTTGTCTTGAAGGCTGTA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:133659421..133659537 26863196 MeRIP-seq:(Medium) rs949995206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85996,RMVar_hsa_circ_369333,RMVar_hsa_circ_221433,RMVar_hsa_circ_221434 99750 RMVar_ID_99750 Human_SNP_ID_154034084 m1A Human chr3 - 133661742 133661742 133661742 AACGAGGTAAGTGAGGCGCGGAGTGGGGACACAGCTCCTCCCCAGCCCCAACTGGGGTTCGCGAT AACGAGGTAAGTGAGGCGCGGAGTGGGGACACGGCTCCTCCCCAGCCCCAACTGGGGTTCGCGAT T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:133661740..133661865 26863196 MeRIP-seq:(Medium) rs538812418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22363981 RMVar_hsa_circ_85996,RMVar_hsa_circ_221434 99751 RMVar_ID_99751 Human_SNP_ID_154034085 m1A Human chr3 - 133661742 133661742 133661742 AACGAGGTAAGTGAGGCGCGGAGTGGGGACACAGCTCCTCCCCAGCCCCAACTGGGGTTCGCGAT AACGAGGTAAGTGAGGCGCGGAGTGGGGACACCGCTCCTCCCCAGCCCCAACTGGGGTTCGCGAT T G TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:133661740..133661865 26863196 MeRIP-seq:(Medium) rs538812418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22363981 RMVar_hsa_circ_85996,RMVar_hsa_circ_221434 99752 RMVar_ID_99752 Human_SNP_ID_154069193 m1A Human chr3 - 133805874 133805874 133805874 GGAAGGTGCCCCCGGCACCGCCGCCATCTGCCACCCGGCGCGAGTCCGCGGAAGCCATGGATGAG GGAAGGTGCCCCCGGCACCGCCGCCATCTGCCCCCCGGCGCGAGTCCGCGGAAGCCATGGATGAG T G AC080128.2 Ensembl:ENSG00000285908 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:133805826..133805975;chr3:133805826..133805946 26863196 MeRIP-seq:(Medium) rs1312148917 Functional Loss SNV dbSNP153 33..33 33 - - - 99753 RMVar_ID_99753 Human_SNP_ID_154072689 m1A Human chr3 - 133819980 133819980 133819980 TTAACAAAGGGAAGATACAGGCATCAGATAAAAGGTACTTGTTTGAAAGGCAGCCATAAGGGAGA TTAACAAAGGGAAGATACAGGCATCAGATAAAGGGTACTTGTTTGAAAGGCAGCCATAAGGGAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:133819932..133820032 32194978 MeRIP-seq:(Medium) rs565111503 Functional Loss SNV dbSNP153 33..33 33 - - - 99754 RMVar_ID_99754 Human_SNP_ID_154091312 m1A Human chr3 - 133895709 133895709 133895709 AGAGCGCGCCCCTCGCACCGCAGCCAGTGCCGACCGCAGCAGCCCAGCCCCAGCCTTCCTCCGCC AGAGCGCGCCCCTCGCACCGCAGCCAGTGCCGTCCGCAGCAGCCCAGCCCCAGCCTTCCTCCGCC T A RAB6B Ensembl:ENSG00000154917 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:133895472..133895814;chr3:133895438..133895845 26863196 MeRIP-seq:(Medium) rs1315251117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3720917,Human_RBP_ID_9333887 99755 RMVar_ID_99755 Human_SNP_ID_154099534 m1A Human chr3 - 133933478 133933475 133933478 GCCAACGAAGGAGGTCATTCATCAACAAATATATTTATTGGAGACCGACTTTGTGCAAAGCAATG GCCAACGAAGGAGGTCATTCATCAACAAATAT___TATTGGAGACCGACTTTGTGCAAAGCAATG AAAT A SLCO2A1 Ensembl:ENSG00000174640 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1470433180 Functional Loss DEL dbSNP153 33..35 33 - - - 99756 RMVar_ID_99756 Human_SNP_ID_154099535 m1A Human chr3 - 133933478 133933478 133933478 GCCAACGAAGGAGGTCATTCATCAACAAATATATTTATTGGAGACCGACTTTGTGCAAAGCAATG GCCAACGAAGGAGGTCATTCATCAACAAATATGTTTATTGGAGACCGACTTTGTGCAAAGCAATG T C SLCO2A1 Ensembl:ENSG00000174640 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1131598 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13147,GWAS_ID_13148,GWAS_ID_13149 99757 RMVar_ID_99757 Human_SNP_ID_154101689 m1A Human chr3 + 133942706 133942705 133942707 ATGGCCGGGAGCAGGAAGTGGGCACAGGGGACAGGGCACGATCCTGTCTTTGCTGAAGCGGATCC ATGGCCGGGAGCAGGAAGTGGGCACAGGGGAC__GGCACGATCCTGTCTTTGCTGAAGCGGATCC CAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:133942661..133942774 26863196 MeRIP-seq:(Medium) rs1559929211 Functional Loss DEL dbSNP153 33..34 33 - - - 99758 RMVar_ID_99758 Human_SNP_ID_154133001 m1A Human chr3 - 134069433 134069433 134069433 AGTGAGACCAAGAACCCACCAATTCCGGACAGAAGGGCCCAGGGAGCATGGAGTGCAGGGACACT AGTGAGACCAAGAACCCACCAATTCCGGACAGCAGGGCCCAGGGAGCATGGAGTGCAGGGACACT T G RYK Ensembl:ENSG00000163785 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:134069324..134069511 26863196 MeRIP-seq:(Medium) rs564584519 Functional Loss SNV dbSNP153 33..33 33 - - - 99759 RMVar_ID_99759 Human_SNP_ID_154153532 m1A Human chr3 - 134158125 134158125 134158125 TCTGACTCCTCTCCAATCCCACACCATCAGGAAGAAGGTGCCTGTCGGGGCTCACTTGAAGCCTG TCTGACTCCTCTCCAATCCCACACCATCAGGAGGAAGGTGCCTGTCGGGGCTCACTTGAAGCCTG T C RYK Ensembl:ENSG00000163785 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134158076..134158250 32194978 MeRIP-seq:(Medium) rs1256064502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14629475,Human_RBP_ID_17292492 RMVar_hsa_circ_221465,RMVar_hsa_circ_86861,RMVar_hsa_circ_221464,RMVar_hsa_circ_106226,RMVar_hsa_circ_265661,RMVar_hsa_circ_221466,RMVar_hsa_circ_221467,RMVar_hsa_circ_221469,RMVar_hsa_circ_376534,RMVar_hsa_circ_377321,RMVar_hsa_circ_221468 99760 RMVar_ID_99760 Human_SNP_ID_154153533 m1A Human chr3 - 134158125 134158125 134158125 TCTGACTCCTCTCCAATCCCACACCATCAGGAAGAAGGTGCCTGTCGGGGCTCACTTGAAGCCTG TCTGACTCCTCTCCAATCCCACACCATCAGGACGAAGGTGCCTGTCGGGGCTCACTTGAAGCCTG T G RYK Ensembl:ENSG00000163785 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134158076..134158250 32194978 MeRIP-seq:(Medium) rs1256064502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14629475,Human_RBP_ID_17292492 RMVar_hsa_circ_221465,RMVar_hsa_circ_86861,RMVar_hsa_circ_221464,RMVar_hsa_circ_106226,RMVar_hsa_circ_265661,RMVar_hsa_circ_221466,RMVar_hsa_circ_221467,RMVar_hsa_circ_221469,RMVar_hsa_circ_376534,RMVar_hsa_circ_377321,RMVar_hsa_circ_221468 99761 RMVar_ID_99761 Human_SNP_ID_154175736 m1A Human chr3 + 134250237 134250237 134250237 AGGGCGGCACGAAGGCTGACCCAGAGCTGGGGACCGGGCAGGGACCACACCTCCCAGCCAGCACG AGGGCGGCACGAAGGCTGACCCAGAGCTGGGGCCCGGGCAGGGACCACACCTCCCAGCCAGCACG A C lnc-CEP63-4 RNACentral:URS00008B3222 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134250234..134250407 32194978 MeRIP-seq:(Medium) rs1041912237 Functional Loss SNV dbSNP153 33..33 33 - - - 99762 RMVar_ID_99762 Human_SNP_ID_154175737 m1A Human chr3 + 134250237 134250237 134250237 AGGGCGGCACGAAGGCTGACCCAGAGCTGGGGACCGGGCAGGGACCACACCTCCCAGCCAGCACG AGGGCGGCACGAAGGCTGACCCAGAGCTGGGGGCCGGGCAGGGACCACACCTCCCAGCCAGCACG A G lnc-CEP63-4 RNACentral:URS00008B3222 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134250234..134250407 32194978 MeRIP-seq:(Medium) rs1041912237 Functional Loss SNV dbSNP153 33..33 33 - - - 99763 RMVar_ID_99763 Human_SNP_ID_154201982 m1A Human chr3 - 134357576 134357576 134357576 CCCTTTCCCCAGCCAGACACTCATTCCCATTGACCATCTGGTCCCAGGAGCTCAGGAGGAGGACC CCCTTTCCCCAGCCAGACACTCATTCCCATTGTCCATCTGGTCCCAGGAGCTCAGGAGGAGGACC T A AMOTL2 Ensembl:ENSG00000114019 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134357526..134357575 32194978 MeRIP-seq:(Medium) rs913410936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27313637,Human_RBP_ID_27498348,Human_RBP_ID_27565764 99764 RMVar_ID_99764 Human_SNP_ID_154202801 m1A Human chr3 - 134360325 134360325 134360325 CGCCCTGCGACTGTCAGAACAACTGCGAGAGAAGGAGGAGCAGATCCTGGCGCTGGAGGCCGACA CGCCCTGCGACTGTCAGAACAACTGCGAGAGATGGAGGAGCAGATCCTGGCGCTGGAGGCCGACA T A AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134360126..134360325 32194978 MeRIP-seq:(Medium) rs757068719 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_486186,Human_Splice_Rec_486204,Human_Splice_Rec_486222,Human_Splice_Rec_486234,Human_Splice_Rec_486252 Human_miRNA_ID_3116373 RMVar_hsa_circ_17488,RMVar_hsa_circ_99655,RMVar_hsa_circ_116261,RMVar_hsa_circ_51792,RMVar_hsa_circ_221492,RMVar_hsa_circ_109867,RMVar_hsa_circ_221493,RMVar_hsa_circ_221494,RMVar_hsa_circ_221495 99765 RMVar_ID_99765 Human_SNP_ID_154202811 m1A Human chr3 + 134360352 134360352 134360352 CCTCCTTCTCTCGCAGTTGTTCTGACAGTCGCAGGGCGCTGAGCTCTGGAGACCCACCACTGCCA CCTCCTTCTCTCGCAGTTGTTCTGACAGTCGCCGGGCGCTGAGCTCTGGAGACCCACCACTGCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:134360306..134360456 26863196 MeRIP-seq:(Medium) rs547949613 Functional Loss SNV dbSNP153 33..33 33 - - - 99766 RMVar_ID_99766 Human_SNP_ID_154202812 m1A Human chr3 + 134360352 134360352 134360352 CCTCCTTCTCTCGCAGTTGTTCTGACAGTCGCAGGGCGCTGAGCTCTGGAGACCCACCACTGCCA CCTCCTTCTCTCGCAGTTGTTCTGACAGTCGCGGGGCGCTGAGCTCTGGAGACCCACCACTGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:134360306..134360456 26863196 MeRIP-seq:(Medium) rs547949613 Functional Loss SNV dbSNP153 33..33 33 - - - 99767 RMVar_ID_99767 Human_SNP_ID_154202844 m1A Human chr3 - 134360411 134360411 134360411 TGACCACGGTCTCTACTCCTTGCTCTGCAGAGACAGGCAGGTGCCCCAGGTGGTAGCAGTGGCAG TGACCACGGTCTCTACTCCTTGCTCTGCAGAGGCAGGCAGGTGCCCCAGGTGGTAGCAGTGGCAG T C AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134360176..134360425 32194978 MeRIP-seq:(Medium) rs1159862889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_486186,Human_Splice_Rec_486204,Human_Splice_Rec_486222,Human_Splice_Rec_486234 RMVar_hsa_circ_17488,RMVar_hsa_circ_99655,RMVar_hsa_circ_51792,RMVar_hsa_circ_221492,RMVar_hsa_circ_109867,RMVar_hsa_circ_221494,RMVar_hsa_circ_221495 99768 RMVar_ID_99768 Human_SNP_ID_154204130 m1A Human chr3 + 134364971 134364971 134364971 CTGAGCTCAGGGCTCCCTTTGCCACCCACCCCATGTACCTCTTGAACTGCCCAATAGCTCCTTCA CTGAGCTCAGGGCTCCCTTTGCCACCCACCCCCTGTACCTCTTGAACTGCCCAATAGCTCCTTCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:134364966..134365157 26863196 MeRIP-seq:(Medium) rs977065051 Functional Loss SNV dbSNP153 33..33 33 - - - 99769 RMVar_ID_99769 Human_SNP_ID_154204518 m1A Human chr3 + 134366373 134366373 134366373 CATGGTCTTCTCCAGGGCCTCACGCTTGGAGGAGGCTCTGGTCAGGCTCTCATGGGCCTCAGAGA CATGGTCTTCTCCAGGGCCTCACGCTTGGAGGCGGCTCTGGTCAGGCTCTCATGGGCCTCAGAGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134366301..134366375 32194978 MeRIP-seq:(Medium) rs757243054 Functional Loss SNV dbSNP153 33..33 33 - - - 99770 RMVar_ID_99770 Human_SNP_ID_154204829 m1A Human chr3 - 134367555 134367555 134367555 GCTGAGGGAGAATGCCAGGCTGCAGAGAGACAATGAGCGGCTGCAGAGGGAGCTGGAGAGCTCTG GCTGAGGGAGAATGCCAGGCTGCAGAGAGACAGTGAGCGGCTGCAGAGGGAGCTGGAGAGCTCTG T C AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134367458..134367585 26863196 MeRIP-seq:(Medium) rs757695633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27498356 Human_Splice_Rec_486179,Human_Splice_Rec_486197,Human_Splice_Rec_486215,Human_Splice_Rec_486245 Human_miRNA_ID_2955181 RMVar_hsa_circ_51792,RMVar_hsa_circ_109867,RMVar_hsa_circ_221495,RMVar_hsa_circ_48060,RMVar_hsa_circ_40502 99771 RMVar_ID_99771 Human_SNP_ID_154204920 m1A Human chr3 - 134367756 134367754 134367757 GGTGCCTCCTGTGTTCCTCCAACAGCAGCAGCAGTACCAGTACCTGCAGCAATCTCAGGAGCACC GGTGCCTCCTGTGTTCCTCCAACAGCAGCAG___TACCAGTACCTGCAGCAATCTCAGGAGCACC ACTG A AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134367626..134367825 32194978 MeRIP-seq:(Medium) rs776058189 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_69751 Human_Splice_Rec_486178,Human_Splice_Rec_486196,Human_Splice_Rec_486214,Human_Splice_Rec_486244,Human_Splice_Rec_486262,Human_Splice_Rec_486266 RMVar_hsa_circ_51792,RMVar_hsa_circ_109867,RMVar_hsa_circ_221495,RMVar_hsa_circ_48060,RMVar_hsa_circ_40502 99772 RMVar_ID_99772 Human_SNP_ID_154204921 m1A Human chr3 - 134367756 134367756 134367756 GGTGCCTCCTGTGTTCCTCCAACAGCAGCAGCAGTACCAGTACCTGCAGCAATCTCAGGAGCACC GGTGCCTCCTGTGTTCCTCCAACAGCAGCAGCCGTACCAGTACCTGCAGCAATCTCAGGAGCACC T G AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134367626..134367825 32194978 MeRIP-seq:(Medium) rs369185876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69751 Human_Splice_Rec_486178,Human_Splice_Rec_486196,Human_Splice_Rec_486214,Human_Splice_Rec_486244,Human_Splice_Rec_486262,Human_Splice_Rec_486266 RMVar_hsa_circ_51792,RMVar_hsa_circ_109867,RMVar_hsa_circ_221495,RMVar_hsa_circ_48060,RMVar_hsa_circ_40502 99773 RMVar_ID_99773 Human_SNP_ID_154205944 m1A Human chr3 - 134371445 134371445 134371445 GCCACCGGCCATTGTCCAGGCAGCTGTGTGCAAGCCAAAGAAGCATGAGGACACTGGAAGACTCC GCCACCGGCCATTGTCCAGGCAGCTGTGTGCAGGCCAAAGAAGCATGAGGACACTGGAAGACTCC T C AMOTL2 Ensembl:ENSG00000114019 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:134371394..134371500 26863196 MeRIP-seq:(Medium) rs755726480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9395531 Human_Splice_Rec_486176,Human_Splice_Rec_486194,Human_Splice_Rec_486212,Human_Splice_Rec_486242,Human_Splice_Rec_486260,Human_Splice_Rec_486264,Human_Splice_Rec_486270,Human_Splice_Rec_486272,Human_Splice_Rec_486274,Human_Splice_Rec_486276,Human_Splice_Rec_486278,Human_Splice_Rec_486282 RMVar_hsa_circ_3404,RMVar_hsa_circ_51792 99774 RMVar_ID_99774 Human_SNP_ID_154205952 m1A Human chr3 - 134371467 134371467 134371467 TCCAGGTGCTCTGGGGCCAGGTGCCACCGGCCATTGTCCAGGCAGCTGTGTGCAAGCCAAAGAAG TCCAGGTGCTCTGGGGCCAGGTGCCACCGGCCGTTGTCCAGGCAGCTGTGTGCAAGCCAAAGAAG T C AMOTL2 Ensembl:ENSG00000114019 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134371326..134371500 32194978 MeRIP-seq:(Medium) rs1228872402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9395531 Human_Splice_Rec_486176,Human_Splice_Rec_486194,Human_Splice_Rec_486212,Human_Splice_Rec_486242,Human_Splice_Rec_486260,Human_Splice_Rec_486264,Human_Splice_Rec_486270,Human_Splice_Rec_486272,Human_Splice_Rec_486274,Human_Splice_Rec_486276,Human_Splice_Rec_486278,Human_Splice_Rec_486282 RMVar_hsa_circ_3404,RMVar_hsa_circ_51792 99775 RMVar_ID_99775 Human_SNP_ID_154206498 m1A Human chr3 + 134373485 134373485 134373485 CCTTTCAGACATCAAACGCCTGGGCCTTTACAAAAACCTGCTTCCGCGCCCCCGGCCGCGAACCT CCTTTCAGACATCAAACGCCTGGGCCTTTACAGAAACCTGCTTCCGCGCCCCCGGCCGCGAACCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134373483..134373554 26863196 MeRIP-seq:(Medium) rs867977200 Functional Loss SNV dbSNP153 33..33 33 - - - 99776 RMVar_ID_99776 Human_SNP_ID_154206694 m1A Human chr3 - 134374094 134374094 134374094 CTAGAAACGCGCGGGTCTCTTGGGGCTGGGGGAGAGGGGAGAGGGCCGACTCCGGAGACAACAGC CTAGAAACGCGCGGGTCTCTTGGGGCTGGGGGGGAGGGGAGAGGGCCGACTCCGGAGACAACAGC T C AMOTL2 Ensembl:ENSG00000114019 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134374092..134374163 26863196 MeRIP-seq:(Medium) rs1256797618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_486279 99777 RMVar_ID_99777 Human_SNP_ID_154206778 m1A Human chr3 + 134374398 134374398 134374398 GCAGTCAGACACCACAACCTCCGGCTCGGCCCAGCTCAGCTCGGCGGCGAAGATGTGTTCTCGGC GCAGTCAGACACCACAACCTCCGGCTCGGCCCTGCTCAGCTCGGCGGCGAAGATGTGTTCTCGGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:134374298..134374478;chr3:134374281..134374499;chr3:134374289..134374500 26863196 MeRIP-seq:(Medium) rs897751089 Functional Loss SNV dbSNP153 33..33 33 - - - 99778 RMVar_ID_99778 Human_SNP_ID_154234406 m1A Human chr3 - 134482910 134482910 134482910 TTGGCTTACAGATTTGACAAGATCAAAGCTGCAGGAAAATGGACAGTGAGGTTCAGAGAGATGGA TTGGCTTACAGATTTGACAAGATCAAAGCTGCGGGAAAATGGACAGTGAGGTTCAGAGAGATGGA T C ANAPC13 Ensembl:ENSG00000129055 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:134482801..134482950 26863196 MeRIP-seq:(Medium) rs751907598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783254,Human_RBP_ID_937699,Human_RBP_ID_1618342,Human_RBP_ID_1949802,Human_RBP_ID_4757468,Human_RBP_ID_14630976,Human_RBP_ID_17994554,Human_RBP_ID_26347224 Human_Splice_Rec_486284,Human_Splice_Rec_486288,Human_Splice_Rec_486292,Human_Splice_Rec_486296,Human_Splice_Rec_486302 Human_miRNA_ID_2758093 RMVar_hsa_circ_221497,RMVar_hsa_circ_79366 99779 RMVar_ID_99779 Human_SNP_ID_154234407 m1A Human chr3 - 134482910 134482910 134482910 TTGGCTTACAGATTTGACAAGATCAAAGCTGCAGGAAAATGGACAGTGAGGTTCAGAGAGATGGA TTGGCTTACAGATTTGACAAGATCAAAGCTGCCGGAAAATGGACAGTGAGGTTCAGAGAGATGGA T G ANAPC13 Ensembl:ENSG00000129055 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:134482801..134482950 26863196 MeRIP-seq:(Medium) rs751907598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783254,Human_RBP_ID_937699,Human_RBP_ID_1618342,Human_RBP_ID_1949802,Human_RBP_ID_4757468,Human_RBP_ID_14630976,Human_RBP_ID_17994554,Human_RBP_ID_26347224 Human_Splice_Rec_486284,Human_Splice_Rec_486288,Human_Splice_Rec_486292,Human_Splice_Rec_486296,Human_Splice_Rec_486302 Human_miRNA_ID_2758093 RMVar_hsa_circ_221497,RMVar_hsa_circ_79366 99780 RMVar_ID_99780 Human_SNP_ID_154234982 m1A Human chr3 - 134485293 134485293 134485293 TGTCACGTGAGTAAGAAAAGTTTGTTCAGGAAACAGTGGTCGTACTGGGTGACGAGTACTTGGGA TGTCACGTGAGTAAGAAAAGTTTGTTCAGGAAGCAGTGGTCGTACTGGGTGACGAGTACTTGGGA T C ANAPC13 Ensembl:ENSG00000129055 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134485290..134485445 26863196 MeRIP-seq:(Medium) rs1042494145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221497,RMVar_hsa_circ_79366 99781 RMVar_ID_99781 Human_SNP_ID_154240720 m1A Human chr3 + 134507158 134507158 134507158 GTGAAGCAGAACTACAGGAGCTCATGAAACAGATTGACATAATGGTGGCTCATAAAAAATCTGAA GTGAAGCAGAACTACAGGAGCTCATGAAACAGGTTGACATAATGGTGGCTCATAAAAAATCTGAA A G CEP63 Ensembl:ENSG00000182923 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:134507057..134507220 26863196 MeRIP-seq:(Medium) rs1435956003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_486306,Human_Splice_Rec_486336,Human_Splice_Rec_486358,Human_Splice_Rec_486382,Human_Splice_Rec_486392,Human_Splice_Rec_486414,Human_Splice_Rec_486422,Human_Splice_Rec_486446,Human_Splice_Rec_486452,Human_Splice_Rec_486480,Human_Splice_Rec_486506 RMVar_hsa_circ_55766,RMVar_hsa_circ_64923,RMVar_hsa_circ_350690,RMVar_hsa_circ_352427,RMVar_hsa_circ_338542,RMVar_hsa_circ_104545,RMVar_hsa_circ_221498,RMVar_hsa_circ_221499,RMVar_hsa_circ_7781 99782 RMVar_ID_99782 Human_SNP_ID_154240721 m1A Human chr3 - 134507159 134507159 134507159 ATTCAGATTTTTTATGAGCCACCATTATGTCAATCTGTTTCATGAGCTCCTGTAGTTCTGCTTCA ATTCAGATTTTTTATGAGCCACCATTATGTCAGTCTGTTTCATGAGCTCCTGTAGTTCTGCTTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134507070..134507161 26863196 MeRIP-seq:(Medium) rs1183918846 Functional Loss SNV dbSNP153 33..33 33 - - - 99783 RMVar_ID_99783 Human_SNP_ID_553423887 m1A Human chr14 + 45006221 45006221 45006221 TTGGAAGTGTGAAAAAGATAGTCTTCCAATTGATCTTTCAGAATTAAATTTCAAGGATAAAGATT TTGGAAGTGTGAAAAAGATAGTCTTCCAATTGGTCTTTCAGAATTAAATTTCAAGGATAAAGATT A G TOGARAM1 Ensembl:ENSG00000198718 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:45006194..45006272 32194978 MeRIP-seq:(Medium) rs764790254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1510347,Human_Splice_Rec_1510385,Human_Splice_Rec_1510421 RMVar_hsa_circ_6009,RMVar_hsa_circ_295812,RMVar_hsa_circ_319796,RMVar_hsa_circ_359007,RMVar_hsa_circ_269828,RMVar_hsa_circ_166180,RMVar_hsa_circ_13877,RMVar_hsa_circ_28338,RMVar_hsa_circ_166176,RMVar_hsa_circ_166178,RMVar_hsa_circ_166179,RMVar_hsa_circ_166177,RMVar_hsa_circ_324903,RMVar_hsa_circ_307713,RMVar_hsa_circ_334065,RMVar_hsa_circ_348064,RMVar_hsa_circ_355387,RMVar_hsa_circ_325838,RMVar_hsa_circ_288636,RMVar_hsa_circ_166182,RMVar_hsa_circ_166184,RMVar_hsa_circ_166185,RMVar_hsa_circ_166183,RMVar_hsa_circ_166181,RMVar_hsa_circ_166186,RMVar_hsa_circ_166188,RMVar_hsa_circ_287223,RMVar_hsa_circ_329149,RMVar_hsa_circ_366139,RMVar_hsa_circ_315184,RMVar_hsa_circ_277381,RMVar_hsa_circ_166187 99784 RMVar_ID_99784 Human_SNP_ID_553442984 m1A Human chr14 - 45084195 45084194 45084196 GCCATGAGCCGGAGCCTGTGACGACCTAGCCGAAGATGGCACTTCACCGCCTCCGTCCCCACAGC GCCATGAGCCGGAGCCTGTGACGACCTAGCCAAGGATGGCACTTCACCGCCTCCGTCCCCACAGC TTC CTT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:45084148..45084279 26863196 MeRIP-seq:(Medium) rs386777034 Functional Loss MNV dbSNP153 32..34 33 - - - 99785 RMVar_ID_99785 Human_SNP_ID_553445707 m1A Human chr14 - 45095184 45095183 45095184 GGAAACACGAAAAAAAGAGAAATATCTTCCAAATGCCAATAAAATTATTTGGCCTCAACAACACC GGAAACACGAAAAAAAGAGAAATATCTTCCAA_TGCCAATAAAATTATTTGGCCTCAACAACACC AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:45095180..45095245 26863196 MeRIP-seq:(Medium) rs559276585 Functional Loss DEL dbSNP153 33..33 33 - - - 99786 RMVar_ID_99786 Human_SNP_ID_553454638 m1A Human chr14 + 45130799 45130799 45130799 TAATGTTTCCTAATAATTTATGTTCTGCAAGAAACTATAAGGAAAAAAGCTGGGTAATCAAGATA TAATGTTTCCTAATAATTTATGTTCTGCAAGACACTATAAGGAAAAAAGCTGGGTAATCAAGATA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Wild Type;HTR8/Svneo,Normoxia chr14:45130676..45130869;chr14:45121599..45130914 26863410,32194978 MeRIP-seq:(Medium) rs1334973845 Functional Loss SNV dbSNP153 33..33 33 - - - 99787 RMVar_ID_99787 Human_SNP_ID_553454641 m1A Human chr14 - 45130802 45130802 45130802 AGTTATCTTGATTACCCAGCTTTTTTCCTTATAGTTTCTTGCAGAACATAAATTATTAGGAAACA AGTTATCTTGATTACCCAGCTTTTTTCCTTATTGTTTCTTGCAGAACATAAATTATTAGGAAACA T A FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr14:45130751..45130825;chr14:45130716..45130867 26863196,26863410,32194978 MeRIP-seq:(Medium) rs1433421943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40641,Human_RBP_ID_1493907,Human_RBP_ID_25098324,Human_RBP_ID_26624956 99788 RMVar_ID_99788 Human_SNP_ID_553456867 m1A Human chr14 + 45138066 45138066 45138066 GTGGAGAGCAGGTTTAGGGGGAACGTGGAAAGATGATTTAGATGTGTTGAGTTTGAGGTGTCTAT GTGGAGAGCAGGTTTAGGGGGAACGTGGAAAGGTGATTTAGATGTGTTGAGTTTGAGGTGTCTAT A G FANCM Ensembl:ENSG00000187790 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:45138015..45138137 26863196 MeRIP-seq:(Medium) rs987906599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231473 RMVar_hsa_circ_348217,RMVar_hsa_circ_61109 99789 RMVar_ID_99789 Human_SNP_ID_554620472 m1A Human chr14 + 49583601 49583601 49583601 AACTGAAGGGTTTTTTCAAATGTTTATTTTATATACAAAGAATTATCATGGTTTTTCATTGAGTA AACTGAAGGGTTTTTTCAAATGTTTATTTTATGTACAAAGAATTATCATGGTTTTTCATTGAGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:49583576..49583600 26863196 MeRIP-seq:(Medium) rs1442048567 Functional Loss SNV dbSNP153 33..33 33 - - - 99790 RMVar_ID_99790 Human_SNP_ID_554620478 m1A Human chr14 - 49583627 49583627 49583627 TCCTTCAGAGGATTATCCGGGGCATCTACTCAATGAAAAACCATGATAATTCTTTGTATATAAAA TCCTTCAGAGGATTATCCGGGGCATCTACTCATTGAAAAACCATGATAATTCTTTGTATATAAAA T A RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr14:49583576..49583700;chr14:49583576..49583650 32194978 MeRIP-seq:(Medium) rs757490523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40524,Human_RBP_ID_269596,Human_RBP_ID_446232,Human_RBP_ID_757551,Human_RBP_ID_998450,Human_RBP_ID_1172125,Human_RBP_ID_1275041,Human_RBP_ID_1361504,Human_RBP_ID_1494076,Human_RBP_ID_1819386,Human_RBP_ID_3450223,Human_RBP_ID_4293976,Human_RBP_ID_5112372,Human_RBP_ID_5140756,Human_RBP_ID_5175931,Human_RBP_ID_5463377,Human_RBP_ID_6351342,Human_RBP_ID_8404292,Human_RBP_ID_9042113,Human_RBP_ID_12337899,Human_RBP_ID_17187275,Human_RBP_ID_17247194,Human_RBP_ID_17362002,Human_RBP_ID_17479063,Human_RBP_ID_17651112,Human_RBP_ID_17687206,Human_RBP_ID_17848775,Human_RBP_ID_18199506,Human_RBP_ID_18207113,Human_RBP_ID_18273545,Human_RBP_ID_18650921,Human_RBP_ID_21886732,Human_RBP_ID_22438495,Human_RBP_ID_22495489,Human_RBP_ID_22797910,Human_RBP_ID_23126898,Human_RBP_ID_23208523,Human_RBP_ID_23271885,Human_RBP_ID_24367117,Human_RBP_ID_24410383,Human_RBP_ID_24472897,Human_RBP_ID_26428623,Human_RBP_ID_26625127,Human_RBP_ID_26748411,Human_RBP_ID_26924398,Human_RBP_ID_27155379,Human_RBP_ID_27226756,Human_RBP_ID_27431314,Human_RBP_ID_27644813 Human_Splice_Rec_1511298,Human_Splice_Rec_1511304,Human_Splice_Rec_1511306,Human_Splice_Rec_1511310 Human_miRNA_ID_2140181,Human_miRNA_ID_2140182,Human_miRNA_ID_2276880,Human_miRNA_ID_2276881 RMVar_hsa_circ_114563,RMVar_hsa_circ_91273,RMVar_hsa_circ_120290,RMVar_hsa_circ_124743,RMVar_hsa_circ_166277,RMVar_hsa_circ_166278,RMVar_hsa_circ_99596,RMVar_hsa_circ_166280,RMVar_hsa_circ_166281,RMVar_hsa_circ_166279 99791 RMVar_ID_99791 Human_SNP_ID_554620479 m1A Human chr14 - 49583627 49583627 49583627 TCCTTCAGAGGATTATCCGGGGCATCTACTCAATGAAAAACCATGATAATTCTTTGTATATAAAA TCCTTCAGAGGATTATCCGGGGCATCTACTCAGTGAAAAACCATGATAATTCTTTGTATATAAAA T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr14:49583576..49583700;chr14:49583576..49583650 32194978 MeRIP-seq:(Medium) rs757490523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40524,Human_RBP_ID_269596,Human_RBP_ID_446232,Human_RBP_ID_757551,Human_RBP_ID_998450,Human_RBP_ID_1172125,Human_RBP_ID_1275041,Human_RBP_ID_1361504,Human_RBP_ID_1494076,Human_RBP_ID_1819386,Human_RBP_ID_3450223,Human_RBP_ID_4293976,Human_RBP_ID_5112372,Human_RBP_ID_5140756,Human_RBP_ID_5175931,Human_RBP_ID_5463377,Human_RBP_ID_6351342,Human_RBP_ID_8404292,Human_RBP_ID_9042113,Human_RBP_ID_12337899,Human_RBP_ID_17187275,Human_RBP_ID_17247194,Human_RBP_ID_17362002,Human_RBP_ID_17479063,Human_RBP_ID_17651112,Human_RBP_ID_17687206,Human_RBP_ID_17848775,Human_RBP_ID_18199506,Human_RBP_ID_18207113,Human_RBP_ID_18273545,Human_RBP_ID_18650921,Human_RBP_ID_21886732,Human_RBP_ID_22438495,Human_RBP_ID_22495489,Human_RBP_ID_22797910,Human_RBP_ID_23126898,Human_RBP_ID_23208523,Human_RBP_ID_23271885,Human_RBP_ID_24367117,Human_RBP_ID_24410383,Human_RBP_ID_24472897,Human_RBP_ID_26428623,Human_RBP_ID_26625127,Human_RBP_ID_26748411,Human_RBP_ID_26924398,Human_RBP_ID_27155379,Human_RBP_ID_27226756,Human_RBP_ID_27431314,Human_RBP_ID_27644813 Human_Splice_Rec_1511298,Human_Splice_Rec_1511304,Human_Splice_Rec_1511306,Human_Splice_Rec_1511310 Human_miRNA_ID_2140181,Human_miRNA_ID_2140182,Human_miRNA_ID_2276880,Human_miRNA_ID_2276881 RMVar_hsa_circ_114563,RMVar_hsa_circ_91273,RMVar_hsa_circ_120290,RMVar_hsa_circ_124743,RMVar_hsa_circ_166277,RMVar_hsa_circ_166278,RMVar_hsa_circ_99596,RMVar_hsa_circ_166280,RMVar_hsa_circ_166281,RMVar_hsa_circ_166279 99792 RMVar_ID_99792 Human_SNP_ID_554621129 m1A Human chr14 - 49585390 49585390 49585390 ATTTTCTAACCAAATATATGTATTAACCGCTGACCCCAAGTTTTTTTTTTTTTTTTTTTGAGTCG ATTTTCTAACCAAATATATGTATTAACCGCTGCCCCCAAGTTTTTTTTTTTTTTTTTTTGAGTCG T G RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:49585385..49585517 26863196 MeRIP-seq:(Medium) rs1378065266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12337978 RMVar_hsa_circ_114563,RMVar_hsa_circ_91273,RMVar_hsa_circ_124743,RMVar_hsa_circ_166277,RMVar_hsa_circ_166278,RMVar_hsa_circ_99596,RMVar_hsa_circ_166280,RMVar_hsa_circ_166281 99793 RMVar_ID_99793 Human_SNP_ID_554621697 m1A Human chr14 - 49586607 49586607 49586607 ATCCTCCAGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGCGCCACCGCGCCCGGCGGTCG ATCCTCCAGCCTCAGCCTCCCGAGTAGCTGGGGCTACAGGCACGCGCCACCGCGCCCGGCGGTCG T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:49586566..49586892 26863196 MeRIP-seq:(Medium) rs1303484391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 99794 RMVar_ID_99794 Human_SNP_ID_554621738 m1A Human chr14 - 49586643 49586643 49586643 TAGCGCACTACAGCCCAGAACTCCTGGACTCAAGCGATCCTCCAGCCTCAGCCTCCCGAGTAGCT TAGCGCACTACAGCCCAGAACTCCTGGACTCACGCGATCCTCCAGCCTCAGCCTCCCGAGTAGCT T G RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:49586576..49586675 26863196 MeRIP-seq:(Medium) rs1322213662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 99795 RMVar_ID_99795 Human_SNP_ID_554621741 m1A Human chr14 - 49586648 49586648 49586648 CGGCATAGCGCACTACAGCCCAGAACTCCTGGACTCAAGCGATCCTCCAGCCTCAGCCTCCCGAG CGGCATAGCGCACTACAGCCCAGAACTCCTGGGCTCAAGCGATCCTCCAGCCTCAGCCTCCCGAG T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:49586599..49586857 26863196 MeRIP-seq:(Medium) rs1141766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 99796 RMVar_ID_99796 Human_SNP_ID_554621745 m1A Human chr14 + 49586651 49586651 49586651 GGGAGGCTGAGGCTGGAGGATCGCTTGAGTCCAGGAGTTCTGGGCTGTAGTGCGCTATGCCGATC GGGAGGCTGAGGCTGGAGGATCGCTTGAGTCCCGGAGTTCTGGGCTGTAGTGCGCTATGCCGATC A C RN7SL1 Ensembl:ENSG00000276168 Other exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr14:49586601..49586859;chr14:49586601..49586806 26863196 MeRIP-seq:(Medium) rs925182316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446267,Human_RBP_ID_3470192,Human_RBP_ID_5095641,Human_RBP_ID_9042120,Human_RBP_ID_18199507,Human_RBP_ID_18206936,Human_RBP_ID_23623623,Human_RBP_ID_27431320 Human_miRNA_ID_3179796,Human_miRNA_ID_3181746,Human_miRNA_ID_3181860,Human_miRNA_ID_3181973,Human_miRNA_ID_3182085,Human_miRNA_ID_3182199,Human_miRNA_ID_3182312,Human_miRNA_ID_3182631,Human_miRNA_ID_3182742,Human_miRNA_ID_3184519 99797 RMVar_ID_99797 Human_SNP_ID_554621746 m1A Human chr14 + 49586651 49586651 49586651 GGGAGGCTGAGGCTGGAGGATCGCTTGAGTCCAGGAGTTCTGGGCTGTAGTGCGCTATGCCGATC GGGAGGCTGAGGCTGGAGGATCGCTTGAGTCCGGGAGTTCTGGGCTGTAGTGCGCTATGCCGATC A G RN7SL1 Ensembl:ENSG00000276168 Other exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr14:49586601..49586859;chr14:49586601..49586806 26863196 MeRIP-seq:(Medium) rs925182316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446267,Human_RBP_ID_3470192,Human_RBP_ID_5095641,Human_RBP_ID_9042120,Human_RBP_ID_18199507,Human_RBP_ID_18206936,Human_RBP_ID_23623623,Human_RBP_ID_27431320 Human_miRNA_ID_3179796,Human_miRNA_ID_3181746,Human_miRNA_ID_3181860,Human_miRNA_ID_3181973,Human_miRNA_ID_3182085,Human_miRNA_ID_3182199,Human_miRNA_ID_3182312,Human_miRNA_ID_3182631,Human_miRNA_ID_3182742,Human_miRNA_ID_3184519 99798 RMVar_ID_99798 Human_SNP_ID_554621776 m1A Human chr14 - 49586687 49586687 49586687 GTCACCATATTGATGCCGAACTTAGTGCGGACACCCGATCGGCATAGCGCACTACAGCCCAGAAC GTCACCATATTGATGCCGAACTTAGTGCGGACGCCCGATCGGCATAGCGCACTACAGCCCAGAAC T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:49586576..49586900 26863410 MeRIP-seq:(Medium) rs993731562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 99799 RMVar_ID_99799 Human_SNP_ID_554625254 m1A Human chr14 + 49599019 49599019 49599019 AGCCAGCTTGACGTGGTTGTGGCCGTTGGGCGAGATGAAGCTACACTGTGAGGTGGAGGTGATCA AGCCAGCTTGACGTGGTTGTGGCCGTTGGGCGCGATGAAGCTACACTGTGAGGTGGAGGTGATCA A C LRR1 Ensembl:ENSG00000165501 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:49598915..49599225 26863196 MeRIP-seq:(Medium) rs1293228208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883357,Human_RBP_ID_1494097,Human_RBP_ID_4293989,Human_RBP_ID_9368925 Human_miRNA_ID_2228643,Human_miRNA_ID_2504621 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99800 RMVar_ID_99800 Human_SNP_ID_554625265 m1A Human chr14 + 49599048 49599048 49599048 GCGAGATGAAGCTACACTGTGAGGTGGAGGTGATCAGCCGGCACTTGCCCGCCTTGGGGCTTAGG GCGAGATGAAGCTACACTGTGAGGTGGAGGTGGTCAGCCGGCACTTGCCCGCCTTGGGGCTTAGG A G LRR1 Ensembl:ENSG00000165501 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:49599001..49599175 26863196 MeRIP-seq:(Medium) rs775229347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1494097,Human_RBP_ID_4308291,Human_RBP_ID_9368925,Human_RBP_ID_22044518 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99801 RMVar_ID_99801 Human_SNP_ID_554625299 m1A Human chr14 + 49599124 49599124 49599124 GGGCGTCCGAGCCGTGTTGAGCCTCTGTCAGCAGACTTCCAGGAGTCAGCCGCCGGTCCGAGCCT GGGCGTCCGAGCCGTGTTGAGCCTCTGTCAGCCGACTTCCAGGAGTCAGCCGCCGGTCCGAGCCT A C LRR1 Ensembl:ENSG00000165501 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:49598815..49599156 26863196 MeRIP-seq:(Medium) rs866827797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446272,Human_RBP_ID_1494100,Human_RBP_ID_4308291,Human_RBP_ID_22044518 Human_Splice_Rec_1511317,Human_Splice_Rec_1511321,Human_Splice_Rec_1511331,Human_Splice_Rec_1511337 Human_miRNA_ID_2454233,Human_miRNA_ID_2949372 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99802 RMVar_ID_99802 Human_SNP_ID_554625590 m1A Human chr14 - 49600022 49600022 49600022 CCACCGCCCCGTCGCCGACCACCACGCACTTGAGCATCAGCGCGCCGGGCCCGTGAGCCATGATG CCACCGCCCCGTCGCCGACCACCACGCACTTGGGCATCAGCGCGCCGGGCCCGTGAGCCATGATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:49600017..49600164 26863196 MeRIP-seq:(Medium) rs1396270357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99803 RMVar_ID_99803 Human_SNP_ID_554631412 m1A Human chr14 - 49619126 49619126 49619126 TTAAATATTTTACTACAGTTTTCATCATATAGACAAAACAGCCCTGCTGCAAAGATGGTCAACGT TTAAATATTTTACTACAGTTTTCATCATATAGGCAAAACAGCCCTGCTGCAAAGATGGTCAACGT T C RPL36AL Ensembl:ENSG00000165502 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:49618701..49619150 32194978 MeRIP-seq:(Medium) rs771615755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446306,Human_RBP_ID_1494132,Human_RBP_ID_1819417,Human_RBP_ID_4308292,Human_RBP_ID_8404336,Human_RBP_ID_22495494,Human_RBP_ID_26808035 Human_Splice_Rec_1511346 Human_miRNA_ID_2222454,Human_miRNA_ID_2485509,Human_miRNA_ID_3073885 RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99804 RMVar_ID_99804 Human_SNP_ID_554631421 m1A Human chr14 - 49619142 49619142 49619142 CGTCTGCTATCTTATTTTAAATATTTTACTACAGTTTTCATCATATAGACAAAACAGCCCTGCTG CGTCTGCTATCTTATTTTAAATATTTTACTACGGTTTTCATCATATAGACAAAACAGCCCTGCTG T C RPL36AL Ensembl:ENSG00000165502 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:49619101..49619150 26863196 MeRIP-seq:(Medium) rs377067013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99805 RMVar_ID_99805 Human_SNP_ID_554631858 m1A Human chr14 - 49620553 49620553 49620553 CCAGGTGTCGGGCGCTGTTTCTCGGTAAGCTAAGAACGAGGCTGTAGCGGCTCCAATAGGAGCCT CCAGGTGTCGGGCGCTGTTTCTCGGTAAGCTACGAACGAGGCTGTAGCGGCTCCAATAGGAGCCT T G RPL36AL Ensembl:ENSG00000165502 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:49620551..49620625 32194978 MeRIP-seq:(Medium) rs984072459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19064018 Human_miRNA_ID_2895529 RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99806 RMVar_ID_99806 Human_SNP_ID_554632237 m1A Human chr14 + 49621347 49621347 49621347 TGGTGGCCGCCTGCGGCTTCGTCCTCTGGAGCAGCAATGGGCGACAAAGGAAGAACGAGGCCCTC TGGTGGCCGCCTGCGGCTTCGTCCTCTGGAGCGGCAATGGGCGACAAAGGAAGAACGAGGCCCTC A G MGAT2 Ensembl:ENSG00000168282 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:49621092..49621555 32194978 MeRIP-seq:(Medium) rs1023249434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1172136,Human_RBP_ID_4307908 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99807 RMVar_ID_99807 Human_SNP_ID_554632459 m1A Human chr14 + 49621813 49621813 49621813 GGTTCTGCAGGTGTTCTTTCCTTTCAGCATTCAGTTGTACCCTAACGAGTTTCCAGGTAGTGACC GGTTCTGCAGGTGTTCTTTCCTTTCAGCATTCGGTTGTACCCTAACGAGTTTCCAGGTAGTGACC A G MGAT2 Ensembl:ENSG00000168282 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:49621640..49622049 32194978 MeRIP-seq:(Medium) rs772527368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1494157,Human_RBP_ID_22044524,Human_RBP_ID_22186421,Human_RBP_ID_26924468,Human_RBP_ID_27226804 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99808 RMVar_ID_99808 Human_SNP_ID_554636054 m1A Human chr14 - 49633951 49633951 49633951 ACCCGCGAGGAGTCGCGCGGAGGACGGAGGCCACGATACCTGCGTGGCTGGGGCTGCGGGCTCCG ACCCGCGAGGAGTCGCGCGGAGGACGGAGGCCGCGATACCTGCGTGGCTGGGGCTGCGGGCTCCG T C DNAAF2 Ensembl:ENSG00000165506 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:49633709..49633972;chr14:49633625..49634004 26863196 MeRIP-seq:(Medium) rs1364926032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99809 RMVar_ID_99809 Human_SNP_ID_554636206 m1A Human chr14 + 49634191 49634191 49634191 CGCGGCCATCGTCCACTGGGTACGGGAGCGAGAGCCGCAGCCGGTAGTCAGGTTTCCTCGAGTCG CGCGGCCATCGTCCACTGGGTACGGGAGCGAGCGCCGCAGCCGGTAGTCAGGTTTCCTCGAGTCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:49634143..49634539 26863196 MeRIP-seq:(Medium) rs767024971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99810 RMVar_ID_99810 Human_SNP_ID_554636302 m1A Human chr14 - 49634350 49634350 49634350 CGTGGTGCAGCGCCACCACGTGGACCTCCAGGATTACCGCTGCTCCAGGGACTCAGCCCCGAGCC CGTGGTGCAGCGCCACCACGTGGACCTCCAGGGTTACCGCTGCTCCAGGGACTCAGCCCCGAGCC T C DNAAF2 Ensembl:ENSG00000165506 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:49634340..49634440 26863410 MeRIP-seq:(Medium) rs1186400886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99811 RMVar_ID_99811 Human_SNP_ID_554636831 m1A Human chr14 - 49635249 49635249 49635249 AAGGCTCAATTTTCCAGCCGTTACCGACCTCCACCGCGTCACTGTACGCTGCCCAGAAACTCTGA AAGGCTCAATTTTCCAGCCGTTACCGACCTCCTCCGCGTCACTGTACGCTGCCCAGAAACTCTGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:49635202..49635326 26863196 MeRIP-seq:(Medium) rs761565159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99812 RMVar_ID_99812 Human_SNP_ID_554646748 m1A Human chr14 + 49672834 49672834 49672834 CTCTTGTCTTTTTATCACTTCTCTTTCTCCCAAGGTCTCATCCTTGCAGTTCCATTTTTTACTCT CTCTTGTCTTTTTATCACTTCTCTTTCTCCCACGGTCTCATCCTTGCAGTTCCATTTTTTACTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:49672829..49673105 26863196 MeRIP-seq:(Medium) rs764877989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99813 RMVar_ID_99813 Human_SNP_ID_554646763 m1A Human chr14 - 49672913 49672913 49672913 GAGAGTATCAAGTGAAGTGTACATCTGGAGCTATGGAAAGAGAGTTGGTAGCAAGAGAGAGATTT GAGAGTATCAAGTGAAGTGTACATCTGGAGCTCTGGAAAGAGAGTTGGTAGCAAGAGAGAGATTT T G POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:49672862..49673072 26863196 MeRIP-seq:(Medium) rs984151389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12338953 RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290,RMVar_hsa_circ_5274,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_320659,RMVar_hsa_circ_375779,RMVar_hsa_circ_166307,RMVar_hsa_circ_374922,RMVar_hsa_circ_271031,RMVar_hsa_circ_39703,RMVar_hsa_circ_30732,RMVar_hsa_circ_166314,RMVar_hsa_circ_166315,RMVar_hsa_circ_271868,RMVar_hsa_circ_96018,RMVar_hsa_circ_166317,RMVar_hsa_circ_166318,RMVar_hsa_circ_341465,RMVar_hsa_circ_61326,RMVar_hsa_circ_166319,RMVar_hsa_circ_35352,RMVar_hsa_circ_281068,RMVar_hsa_circ_370665,RMVar_hsa_circ_166320 99814 RMVar_ID_99814 Human_SNP_ID_554652315 m1A Human chr14 + 49693186 49693161 49693187 GGGGTTGTGGCGCGGCAAGCGGCGGGCCAGCGACGGCGCGAATGGCGGACTCTCAGCTGTTCTGT GGGGTTGT__________________________GGCGCGAATGGCGGACTCTCAGCTGTTCTGT TGGCGCGGCAAGCGGCGGGCCAGCGAC T KLHDC1 Ensembl:ENSG00000197776 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:49693135..49693331 26863196 MeRIP-seq:(Medium) rs1314931420 Functional Loss DEL dbSNP153 9..34 33 - - - RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99815 RMVar_ID_99815 Human_SNP_ID_554652322 m1A Human chr14 + 49693171 49693171 49693171 GCCGCCGGGCGGGCAGGGGTTGTGGCGCGGCAAGCGGCGGGCCAGCGACGGCGCGAATGGCGGAC GCCGCCGGGCGGGCAGGGGTTGTGGCGCGGCAGGCGGCGGGCCAGCGACGGCGCGAATGGCGGAC A G KLHDC1 Ensembl:ENSG00000197776 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:49693149..49693291 26863196 MeRIP-seq:(Medium) rs1210320706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99816 RMVar_ID_99816 Human_SNP_ID_554652338 m1A Human chr14 + 49693186 49693186 49693186 GGGGTTGTGGCGCGGCAAGCGGCGGGCCAGCGACGGCGCGAATGGCGGACTCTCAGCTGTTCTGT GGGGTTGTGGCGCGGCAAGCGGCGGGCCAGCGGCGGCGCGAATGGCGGACTCTCAGCTGTTCTGT A G KLHDC1 Ensembl:ENSG00000197776 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:49693135..49693331 26863196 MeRIP-seq:(Medium) rs751445113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 99817 RMVar_ID_99817 Human_SNP_ID_554672659 m1A Human chr14 - 49768211 49768211 49768211 GCGGAGCCGGGCGGCGGCGGCGCGGGCCCGGGACTCGGGGCACTGCAGGGAAGCGGTCCGCGTCG GCGGAGCCGGGCGGCGGCGGCGCGGGCCCGGGCCTCGGGGCACTGCAGGGAAGCGGTCCGCGTCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:49768167..49768276 26863196 MeRIP-seq:(Medium) rs1001548919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 99818 RMVar_ID_99818 Human_SNP_ID_554699455 m1A Human chr14 - 49862575 49862575 49862575 GCGCCTGTGAATAGCCACTGCACTCCAGCCTGAGCAACATAGCGAGACCCCGTCTCTTTTGCCCC GCGCCTGTGAATAGCCACTGCACTCCAGCCTGGGCAACATAGCGAGACCCCGTCTCTTTTGCCCC T C RN7SL2,AL627171.4 Ensembl:ENSG00000274012,Ensembl:ENSG00000282885 Other,lincRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEK293T cell line,total RNA chr14:49862551..49862637;chr14:49862532..49862666 31548705,26863196 m1A-IP-seq:(High) rs563135372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269620,Human_RBP_ID_276399,Human_RBP_ID_446386,Human_RBP_ID_998480,Human_RBP_ID_1063958,Human_RBP_ID_1129551,Human_RBP_ID_1172146,Human_RBP_ID_1361527,Human_RBP_ID_1494256,Human_RBP_ID_1819526,Human_RBP_ID_3450484,Human_RBP_ID_4312754,Human_RBP_ID_5095640,Human_RBP_ID_5258287,Human_RBP_ID_5274421,Human_RBP_ID_5287008,Human_RBP_ID_5418150,Human_RBP_ID_5439086,Human_RBP_ID_5463390,Human_RBP_ID_5493597,Human_RBP_ID_5563217,Human_RBP_ID_6351985,Human_RBP_ID_8076684,Human_RBP_ID_8182279,Human_RBP_ID_8250199,Human_RBP_ID_8404442,Human_RBP_ID_8794518,Human_RBP_ID_9042175,Human_RBP_ID_9281671,Human_RBP_ID_12339841,Human_RBP_ID_17481280,Human_RBP_ID_17669385,Human_RBP_ID_17687218,Human_RBP_ID_17848878,Human_RBP_ID_18199513,Human_RBP_ID_18206942,Human_RBP_ID_18273592,Human_RBP_ID_18435855,Human_RBP_ID_18512102,Human_RBP_ID_18528344,Human_RBP_ID_18651080,Human_RBP_ID_20002175,Human_RBP_ID_22798611,Human_RBP_ID_22927152,Human_RBP_ID_23110326,Human_RBP_ID_23126913,Human_RBP_ID_23160950,Human_RBP_ID_23307030,Human_RBP_ID_23623906,Human_RBP_ID_26428659,Human_RBP_ID_26748418,Human_RBP_ID_26924562,Human_RBP_ID_27226867,Human_RBP_ID_27431416,Human_RBP_ID_27559018,Human_RBP_ID_27796827 Human_Splice_Rec_1512069,Human_Splice_Rec_1512071 RMVar_hsa_circ_76409,RMVar_hsa_circ_118194,RMVar_hsa_circ_87204,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_126450,RMVar_hsa_circ_166401 99819 RMVar_ID_99819 Human_SNP_ID_554699456 m1A Human chr14 - 49862575 49862575 49862575 GCGCCTGTGAATAGCCACTGCACTCCAGCCTGAGCAACATAGCGAGACCCCGTCTCTTTTGCCCC GCGCCTGTGAATAGCCACTGCACTCCAGCCTGCGCAACATAGCGAGACCCCGTCTCTTTTGCCCC T G RN7SL2,AL627171.4 Ensembl:ENSG00000274012,Ensembl:ENSG00000282885 Other,lincRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEK293T cell line,total RNA chr14:49862551..49862637;chr14:49862532..49862666 31548705,26863196 m1A-IP-seq:(High) rs563135372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269620,Human_RBP_ID_276399,Human_RBP_ID_446386,Human_RBP_ID_998480,Human_RBP_ID_1063958,Human_RBP_ID_1129551,Human_RBP_ID_1172146,Human_RBP_ID_1361527,Human_RBP_ID_1494256,Human_RBP_ID_1819526,Human_RBP_ID_3450484,Human_RBP_ID_4312754,Human_RBP_ID_5095640,Human_RBP_ID_5258287,Human_RBP_ID_5274421,Human_RBP_ID_5287008,Human_RBP_ID_5418150,Human_RBP_ID_5439086,Human_RBP_ID_5463390,Human_RBP_ID_5493597,Human_RBP_ID_5563217,Human_RBP_ID_6351985,Human_RBP_ID_8076684,Human_RBP_ID_8182279,Human_RBP_ID_8250199,Human_RBP_ID_8404442,Human_RBP_ID_8794518,Human_RBP_ID_9042175,Human_RBP_ID_9281671,Human_RBP_ID_12339841,Human_RBP_ID_17481280,Human_RBP_ID_17669385,Human_RBP_ID_17687218,Human_RBP_ID_17848878,Human_RBP_ID_18199513,Human_RBP_ID_18206942,Human_RBP_ID_18273592,Human_RBP_ID_18435855,Human_RBP_ID_18512102,Human_RBP_ID_18528344,Human_RBP_ID_18651080,Human_RBP_ID_20002175,Human_RBP_ID_22798611,Human_RBP_ID_22927152,Human_RBP_ID_23110326,Human_RBP_ID_23126913,Human_RBP_ID_23160950,Human_RBP_ID_23307030,Human_RBP_ID_23623906,Human_RBP_ID_26428659,Human_RBP_ID_26748418,Human_RBP_ID_26924562,Human_RBP_ID_27226867,Human_RBP_ID_27431416,Human_RBP_ID_27559018,Human_RBP_ID_27796827 Human_Splice_Rec_1512069,Human_Splice_Rec_1512071 RMVar_hsa_circ_76409,RMVar_hsa_circ_118194,RMVar_hsa_circ_87204,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_126450,RMVar_hsa_circ_166401 99820 RMVar_ID_99820 Human_SNP_ID_554708122 m1A Human chr14 - 49893725 49893725 49893725 TTTGGATAGCACCTTCCCCATCGCGTCGGAGGAGCCGGGGCCGGGGGCATTCAGGTGTCCCGGGT TTTGGATAGCACCTTCCCCATCGCGTCGGAGGCGCCGGGGCCGGGGGCATTCAGGTGTCCCGGGT T G lnc-NEMF-4 RNACentral:URS0000D59A1E lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:49893551..49893815 26863196 MeRIP-seq:(Medium) rs867958221 Functional Loss SNV dbSNP153 33..33 33 - - - 99821 RMVar_ID_99821 Human_SNP_ID_554708214 m1A Human chr14 - 49893999 49893999 49893999 CCTCATCGATGCGGTCGCGGTCGGCGCAGTCCACTACGAAGATGAGACCTTGGGTCCCAGTGTAG CCTCATCGATGCGGTCGCGGTCGGCGCAGTCCGCTACGAAGATGAGACCTTGGGTCCCAGTGTAG T C lnc-NEMF-4 RNACentral:URS0000D59A1E lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:49893288..49894280 32194978 MeRIP-seq:(Medium) rs1448005974 Functional Loss SNV dbSNP153 33..33 33 - - - 99822 RMVar_ID_99822 Human_SNP_ID_554800226 m1A Human chr14 - 50246273 50246273 50246273 TCAAGGCTACAGTGAGCTGTGTTCATGCCACTATACCCCAGCCTGGGCAACAAAGTGAGTCCCTG TCAAGGCTACAGTGAGCTGTGTTCATGCCACTGTACCCCAGCCTGGGCAACAAAGTGAGTCCCTG T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs758805529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5257965,Human_RBP_ID_25099656 RMVar_hsa_circ_119404,RMVar_hsa_circ_166465,RMVar_hsa_circ_268325,RMVar_hsa_circ_166467,RMVar_hsa_circ_83950,RMVar_hsa_circ_109358,RMVar_hsa_circ_166466,RMVar_hsa_circ_166468 99823 RMVar_ID_99823 Human_SNP_ID_554817074 m1A Human chr14 - 50312150 50312150 50312150 TGAGCGCTGAGGGAGGGGAGCGTGCGTAGGGGATGGTGCCAGCGCTGCGTTATTTGGTTGGTGCC TGAGCGCTGAGGGAGGGGAGCGTGCGTAGGGGGTGGTGCCAGCGCTGCGTTATTTGGTTGGTGCC T C L2HGDH Ensembl:ENSG00000087299 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:50311971..50312200 26863196 MeRIP-seq:(Medium) rs1477101414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756660,Human_RBP_ID_4294495,Human_RBP_ID_17687233,Human_RBP_ID_18417962,Human_RBP_ID_23624260,Human_RBP_ID_27837232 RMVar_hsa_circ_78930,RMVar_hsa_circ_166481 99824 RMVar_ID_99824 Human_SNP_ID_554817077 m1A Human chr14 - 50312155 50312155 50312155 TCTTCTGAGCGCTGAGGGAGGGGAGCGTGCGTAGGGGATGGTGCCAGCGCTGCGTTATTTGGTTG TCTTCTGAGCGCTGAGGGAGGGGAGCGTGCGTCGGGGATGGTGCCAGCGCTGCGTTATTTGGTTG T G L2HGDH Ensembl:ENSG00000087299 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:50312043..50312176 26863196 MeRIP-seq:(Medium) rs1200834222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756660,Human_RBP_ID_4294495,Human_RBP_ID_18417962,Human_RBP_ID_18651235,Human_RBP_ID_23624260,Human_RBP_ID_27837232 RMVar_hsa_circ_78930,RMVar_hsa_circ_166481 99825 RMVar_ID_99825 Human_SNP_ID_554864204 m1A Human chr14 - 50504850 50504850 50504850 ATTTTTGTTTTTATTTTATTTTTAGGCCAGAAATGTACACACAGGAGAGCTGGCTGCAGTAAAAA ATTTTTGTTTTTATTTTATTTTTAGGCCAGAATTGTACACACAGGAGAGCTGGCTGCAGTAAAAA T A MAP4K5 Ensembl:ENSG00000012983 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:50486173..50504878 26863196 MeRIP-seq:(Medium) rs1170877901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_276404,Human_RBP_ID_6353520 Human_Splice_Rec_1512708,Human_Splice_Rec_1512709,Human_Splice_Rec_1512788,Human_Splice_Rec_1512789,Human_Splice_Rec_1512812,Human_Splice_Rec_1512813,Human_Splice_Rec_1512828,Human_Splice_Rec_1512829,Human_Splice_Rec_1512837,Human_Splice_Rec_1512842 RMVar_hsa_circ_2345,RMVar_hsa_circ_328481,RMVar_hsa_circ_166518,RMVar_hsa_circ_336203,RMVar_hsa_circ_299467,RMVar_hsa_circ_119320,RMVar_hsa_circ_166527,RMVar_hsa_circ_166528,RMVar_hsa_circ_342926,RMVar_hsa_circ_166533,RMVar_hsa_circ_340735 99826 RMVar_ID_99826 Human_SNP_ID_554864206 m1A Human chr14 - 50504854 50504854 50504854 CAAGATTTTTGTTTTTATTTTATTTTTAGGCCAGAAATGTACACACAGGAGAGCTGGCTGCAGTA CAAGATTTTTGTTTTTATTTTATTTTTAGGCCGGAAATGTACACACAGGAGAGCTGGCTGCAGTA T C MAP4K5 Ensembl:ENSG00000012983 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:50504801..50504875;chr14:50504801..50504931 26863196 MeRIP-seq:(Medium) rs759240996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6353520 Human_Splice_Rec_1512708,Human_Splice_Rec_1512709,Human_Splice_Rec_1512788,Human_Splice_Rec_1512789,Human_Splice_Rec_1512812,Human_Splice_Rec_1512813,Human_Splice_Rec_1512828,Human_Splice_Rec_1512829,Human_Splice_Rec_1512837,Human_Splice_Rec_1512842 RMVar_hsa_circ_2345,RMVar_hsa_circ_328481,RMVar_hsa_circ_166518,RMVar_hsa_circ_336203,RMVar_hsa_circ_299467,RMVar_hsa_circ_119320,RMVar_hsa_circ_166527,RMVar_hsa_circ_166528,RMVar_hsa_circ_342926,RMVar_hsa_circ_166533,RMVar_hsa_circ_340735 99827 RMVar_ID_99827 Human_SNP_ID_554866689 m1A Human chr14 - 50515239 50515239 50515239 AGGCAAGAGAAAGGATAGAGAGGAAACTGTGAACCAGGGGTCATAAAATCTTAAAAGAATAAGGA AGGCAAGAGAAAGGATAGAGAGGAAACTGTGAGCCAGGGGTCATAAAATCTTAAAAGAATAAGGA T C MAP4K5 Ensembl:ENSG00000012983 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:50515237..50515569 26863196 MeRIP-seq:(Medium) rs998605160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119320,RMVar_hsa_circ_166528 99828 RMVar_ID_99828 Human_SNP_ID_554866698 m1A Human chr14 - 50515271 50515271 50515271 GTTCCGGATATTGAAGTCACTAAGAGTGGTGGAGGCAAGAGAAAGGATAGAGAGGAAACTGTGAA GTTCCGGATATTGAAGTCACTAAGAGTGGTGGGGGCAAGAGAAAGGATAGAGAGGAAACTGTGAA T C MAP4K5 Ensembl:ENSG00000012983 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:50515269..50515558 26863196 MeRIP-seq:(Medium) rs888460475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119320,RMVar_hsa_circ_166528 99829 RMVar_ID_99829 Human_SNP_ID_554870695 m1A Human chr14 - 50532000 50532000 50532000 GCCTGCCGCGGACATCCTGAGGCGGAACCCGCAGCAGGACTACGAACTCGTCCAGAGGGTCGGCA GCCTGCCGCGGACATCCTGAGGCGGAACCCGCTGCAGGACTACGAACTCGTCCAGAGGGTCGGCA T A MAP4K5 Ensembl:ENSG00000012983 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50531951..50532075 32194978 MeRIP-seq:(Medium) rs1296277246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_998526,Human_RBP_ID_22926357 Human_Splice_Rec_1512707,Human_Splice_Rec_1512787,Human_Splice_Rec_1512827,Human_Splice_Rec_1512841 RMVar_hsa_circ_119320,RMVar_hsa_circ_166528 99830 RMVar_ID_99830 Human_SNP_ID_554870696 m1A Human chr14 - 50532000 50532000 50532000 GCCTGCCGCGGACATCCTGAGGCGGAACCCGCAGCAGGACTACGAACTCGTCCAGAGGGTCGGCA GCCTGCCGCGGACATCCTGAGGCGGAACCCGCGGCAGGACTACGAACTCGTCCAGAGGGTCGGCA T C MAP4K5 Ensembl:ENSG00000012983 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50531951..50532075 32194978 MeRIP-seq:(Medium) rs1296277246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_998526,Human_RBP_ID_22926357 Human_Splice_Rec_1512707,Human_Splice_Rec_1512787,Human_Splice_Rec_1512827,Human_Splice_Rec_1512841 RMVar_hsa_circ_119320,RMVar_hsa_circ_166528 99831 RMVar_ID_99831 Human_SNP_ID_554870752 m1A Human chr14 - 50532098 50532098 50532098 GGGAAGCGGCGCCGTTCGTGCTTGTTAGCGGGAATCCGGGAGCCGCGGGGTGAGCTGGCGGGGGC GGGAAGCGGCGCCGTTCGTGCTTGTTAGCGGGCATCCGGGAGCCGCGGGGTGAGCTGGCGGGGGC T G MAP4K5 Ensembl:ENSG00000012983 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:50531955..50532202 26863196 MeRIP-seq:(Medium) rs541943270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230851,Human_RBP_ID_446624,Human_RBP_ID_8230616,Human_RBP_ID_9352997,Human_RBP_ID_9370084,Human_RBP_ID_18979645,Human_RBP_ID_26324698 Human_Splice_Rec_1512706,Human_Splice_Rec_1512826,Human_Splice_Rec_1512840 RMVar_hsa_circ_119320,RMVar_hsa_circ_166528 99832 RMVar_ID_99832 Human_SNP_ID_554877168 m1A Human chr14 + 50560219 50560219 50560219 CACCGCCAGCAACCTGCGGCCCCGGAGAAGGCAGCGAGCGCAGTGACAGCGCCTCACCGCCACCA CACCGCCAGCAACCTGCGGCCCCGGAGAAGGCTGCGAGCGCAGTGACAGCGCCTCACCGCCACCA A T ATL1 Ensembl:ENSG00000198513 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:50560169..50560249 26863196 MeRIP-seq:(Medium) rs747467422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1512846,Human_Splice_Rec_1512847,Human_Splice_Rec_1512850,Human_Splice_Rec_1512851,Human_Splice_Rec_1512876,Human_Splice_Rec_1512877,Human_Splice_Rec_1512882,Human_Splice_Rec_1512883,Human_Splice_Rec_1512885,Human_Splice_Rec_1512895,Human_Splice_Rec_1512919,Human_Splice_Rec_1512929 RMVar_hsa_circ_73491,RMVar_hsa_circ_368018,RMVar_hsa_circ_166535 99833 RMVar_ID_99833 Human_SNP_ID_554903103 m1A Human chr14 + 50668079 50668056 50668079 CTCCGCCGGCGCCGCCGCCTCCTTCCCTCCCGAGCCGCCGCCTCCGCCGCCGCCTGTCCGGAGCC CTCCGCCGGC_______________________GCCGCCGCCTCCGCCGCCGCCTGTCCGGAGCC CGCCGCCGCCTCCTTCCCTCCCGA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:50667981..50668132;chr14:50667901..50668350 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1169163714 Functional Loss DEL dbSNP153 11..33 33 - - - 99834 RMVar_ID_99834 Human_SNP_ID_554903111 m1A Human chr14 + 50668079 50668079 50668079 CTCCGCCGGCGCCGCCGCCTCCTTCCCTCCCGAGCCGCCGCCTCCGCCGCCGCCTGTCCGGAGCC CTCCGCCGGCGCCGCCGCCTCCTTCCCTCCCGTGCCGCCGCCTCCGCCGCCGCCTGTCCGGAGCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:50667981..50668132;chr14:50667901..50668350 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1359363547 Functional Loss SNV dbSNP153 33..33 33 - - - 99835 RMVar_ID_99835 Human_SNP_ID_554903115 m1A Human chr14 - 50668089 50668089 50668089 GGCGACCCCGGGCTCCGGACAGGCGGCGGCGGAGGCGGCGGCTCGGGAGGGAAGGAGGCGGCGGC GGCGACCCCGGGCTCCGGACAGGCGGCGGCGGGGGCGGCGGCTCGGGAGGGAAGGAGGCGGCGGC T C SAV1 Ensembl:ENSG00000151748 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr14:50667931..50668331;chr14:50668010..50668182 26863196 MeRIP-seq:(Medium) rs1445294313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231248,Human_RBP_ID_4307924,Human_RBP_ID_23624560 RMVar_hsa_circ_93504,RMVar_hsa_circ_109096,RMVar_hsa_circ_166548,RMVar_hsa_circ_166549 99836 RMVar_ID_99836 Human_SNP_ID_554903148 m1A Human chr14 + 50668182 50668182 50668182 TAAGCGCGCCGGCCGCCGCTCAGTCGCTGGTCAGTTCCTTCCCGGAAGTCGGCCCGCTCTGCGAC TAAGCGCGCCGGCCGCCGCTCAGTCGCTGGTCGGTTCCTTCCCGGAAGTCGGCCCGCTCTGCGAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:50667959..50668200 26863196 MeRIP-seq:(Medium) rs878897459 Functional Loss SNV dbSNP153 33..33 33 - - - 99837 RMVar_ID_99837 Human_SNP_ID_554903183 m1A Human chr14 - 50668271 50668265 50668271 GGTAGCGGTTATTCGGCGGCCCGCGGCGGACCATGGCCCTGGCCCTGGCCCGGCGTCGCTGGGCT GGTAGCGGTTATTCGGCGGCCCGCGGCGGACC______CTGGCCCTGGCCCGGCGTCGCTGGGCT GGGCCAT G SAV1 Ensembl:ENSG00000151748 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr14:50668210..50668307;chr14:50667901..50668350 26863410,26863196 MeRIP-seq:(Medium) rs1416409966 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4294635 Human_miRNA_ID_2681117 RMVar_hsa_circ_93504,RMVar_hsa_circ_109096,RMVar_hsa_circ_166548,RMVar_hsa_circ_166549 99838 RMVar_ID_99838 Human_SNP_ID_554929020 m1A Human chr14 + 50756899 50756899 50756899 TTACATTCCTCTATGACATGATGTACACTCCTAACCCTGGGCACACACTCTTCCAGTGTCTGATT TTACATTCCTCTATGACATGATGTACACTCCTGACCCTGGGCACACACTCTTCCAGTGTCTGATT A G lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50756856..50756957 32194978 MeRIP-seq:(Medium) rs1160857791 Functional Loss SNV dbSNP153 33..33 33 - - - 99839 RMVar_ID_99839 Human_SNP_ID_554929112 m1A Human chr14 - 50757155 50757155 50757155 AGAACTCACTGCAGAGGTTTTCAGGTTGCAGGATGAGCTGAAGAAAATGGAGGAAGTCACTGAAA AGAACTCACTGCAGAGGTTTTCAGGTTGCAGGTTGAGCTGAAGAAAATGGAGGAAGTCACTGAAA T A NIN Ensembl:ENSG00000100503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50757106..50757256 32194978 MeRIP-seq:(Medium) rs1170975783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46869,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_324799,RMVar_hsa_circ_64625,RMVar_hsa_circ_166564,RMVar_hsa_circ_23643,RMVar_hsa_circ_23989,RMVar_hsa_circ_298344,RMVar_hsa_circ_57623,RMVar_hsa_circ_72339,RMVar_hsa_circ_266035,RMVar_hsa_circ_359044,RMVar_hsa_circ_13706 99840 RMVar_ID_99840 Human_SNP_ID_554930174 m1A Human chr14 + 50760173 50760173 50760173 TTGCAGTTGTTTTTTCTCCTCCTCATGCCTGCAAGTGGCCTCATGATGTGCCTCCTTGAGCACTG TTGCAGTTGTTTTTTCTCCTCCTCATGCCTGCTAGTGGCCTCATGATGTGCCTCCTTGAGCACTG A T lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:50760025..50760296 26863196 MeRIP-seq:(Medium) rs1331123454 Functional Loss SNV dbSNP153 33..33 33 - - - 99841 RMVar_ID_99841 Human_SNP_ID_554934568 m1A Human chr14 + 50777071 50777071 50777071 TTCACAAACTTCTTGCAGTTTCTCTTCTATCCAGTCTTGGGGAGGGGAAGATCCACTCTGTGAAG TTCACAAACTTCTTGCAGTTTCTCTTCTATCCGGTCTTGGGGAGGGGAAGATCCACTCTGTGAAG A G lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50776971..50777072 32194978 MeRIP-seq:(Medium) rs755289936 Functional Loss SNV dbSNP153 33..33 33 - - - 99842 RMVar_ID_99842 Human_SNP_ID_554934569 m1A Human chr14 + 50777071 50777071 50777071 TTCACAAACTTCTTGCAGTTTCTCTTCTATCCAGTCTTGGGGAGGGGAAGATCCACTCTGTGAAG TTCACAAACTTCTTGCAGTTTCTCTTCTATCCTGTCTTGGGGAGGGGAAGATCCACTCTGTGAAG A T lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50776971..50777072 32194978 MeRIP-seq:(Medium) rs755289936 Functional Loss SNV dbSNP153 33..33 33 - - - 99843 RMVar_ID_99843 Human_SNP_ID_554947577 m1A Human chr14 + 50831099 50831099 50831099 GGCTTGGCGGCGGCAGCGGGACGGCCGCGCCCAGCGCGCTCGGCTCCCGGCTCGGCCGCGGCCAC GGCTTGGCGGCGGCAGCGGGACGGCCGCGCCCTGCGCGCTCGGCTCCCGGCTCGGCCGCGGCCAC A T lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:50830951..50831119 26863196 MeRIP-seq:(Medium) rs1465752029 Functional Loss SNV dbSNP153 33..33 33 - - - 99844 RMVar_ID_99844 Human_SNP_ID_554964477 m1A Human chr14 - 50894901 50894901 50894901 GGAGGGGAGGCGATAAAAAGATTATAGGGTGGAGGAGCAGAGGCTGAGGAAGAATTGAGGCCTAG GGAGGGGAGGCGATAAAAAGATTATAGGGTGGTGGAGCAGAGGCTGAGGAAGAATTGAGGCCTAG T A PYGL Ensembl:ENSG00000100504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:50894851..50894973 26863196 MeRIP-seq:(Medium) rs1050218612 Functional Loss SNV dbSNP153 33..33 33 - - - 99845 RMVar_ID_99845 Human_SNP_ID_554968181 m1A Human chr14 - 50908953 50908953 50908953 TTTTATCACCCACCCACCCCTACCCCACAGGTACGAGGCAAAAGAATACTATGAGGCACTTCCAG TTTTATCACCCACCCACCCCTACCCCACAGGTGCGAGGCAAAAGAATACTATGAGGCACTTCCAG T C PYGL Ensembl:ENSG00000100504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:50908951..50908975 32194978 MeRIP-seq:(Medium) rs745756440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18980619 Human_Splice_Rec_1513694,Human_Splice_Rec_1513730,Human_Splice_Rec_1513764,Human_Splice_Rec_1513772 RMVar_hsa_circ_166586,RMVar_hsa_circ_72897,RMVar_hsa_circ_123122,RMVar_hsa_circ_358622,RMVar_hsa_circ_378803,RMVar_hsa_circ_319026,RMVar_hsa_circ_105705,RMVar_hsa_circ_59651,RMVar_hsa_circ_166587,RMVar_hsa_circ_65923,RMVar_hsa_circ_166585 99846 RMVar_ID_99846 Human_SNP_ID_554968182 m1A Human chr14 - 50908953 50908953 50908953 TTTTATCACCCACCCACCCCTACCCCACAGGTACGAGGCAAAAGAATACTATGAGGCACTTCCAG TTTTATCACCCACCCACCCCTACCCCACAGGTCCGAGGCAAAAGAATACTATGAGGCACTTCCAG T G PYGL Ensembl:ENSG00000100504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:50908951..50908975 32194978 MeRIP-seq:(Medium) rs745756440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18980619 Human_Splice_Rec_1513694,Human_Splice_Rec_1513730,Human_Splice_Rec_1513764,Human_Splice_Rec_1513772 RMVar_hsa_circ_166586,RMVar_hsa_circ_72897,RMVar_hsa_circ_123122,RMVar_hsa_circ_358622,RMVar_hsa_circ_378803,RMVar_hsa_circ_319026,RMVar_hsa_circ_105705,RMVar_hsa_circ_59651,RMVar_hsa_circ_166587,RMVar_hsa_circ_65923,RMVar_hsa_circ_166585 99847 RMVar_ID_99847 Human_SNP_ID_554968457 m1A Human chr14 + 50909979 50909979 50909979 GGTTCTCTTCCCCAGCTTCTTCTGCCATTTCCACATTGGCCCCATCCATGGTCCCGATAGTTAGG GGTTCTCTTCCCCAGCTTCTTCTGCCATTTCCCCATTGGCCCCATCCATGGTCCCGATAGTTAGG A C lnc-ABHD12B-2 RNACentral:URS0000D5C4B1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:50909928..50910056 26863196 MeRIP-seq:(Medium) rs35831273 Functional Loss SNV dbSNP153 33..33 33 - - - 99848 RMVar_ID_99848 Human_SNP_ID_554969118 m1A Human chr14 - 50912297 50912297 50912297 TCTGGCACCATGCACTGTCTTAACAGGAGAATAAGCTGAAGTTTTCTCAGTTCCTGGAGACGGAG TCTGGCACCATGCACTGTCTTAACAGGAGAATCAGCTGAAGTTTTCTCAGTTCCTGGAGACGGAG T G PYGL Ensembl:ENSG00000100504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:50912246..50914792 32194978 MeRIP-seq:(Medium) rs1187641828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1513686,Human_Splice_Rec_1513722,Human_Splice_Rec_1513756 Human_miRNA_ID_1539778,Human_miRNA_ID_1593716 RMVar_hsa_circ_166586,RMVar_hsa_circ_72897,RMVar_hsa_circ_358622,RMVar_hsa_circ_378803,RMVar_hsa_circ_319026,RMVar_hsa_circ_105705,RMVar_hsa_circ_59651,RMVar_hsa_circ_166587,RMVar_hsa_circ_65923,RMVar_hsa_circ_24566 99849 RMVar_ID_99849 Human_SNP_ID_554972139 m1A Human chr14 - 50924018 50924018 50924018 CCGCCCAGAATTCATGCTGCCTGTGCACTTCTATGGAAAAGTAGAACACACCAACACCGGGACCA CCGCCCAGAATTCATGCTGCCTGTGCACTTCTGTGGAAAAGTAGAACACACCAACACCGGGACCA T C PYGL Ensembl:ENSG00000100504 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:50924001..50924025 26863196 MeRIP-seq:(Medium) rs34096980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39183,Human_RBP_ID_446855,Human_RBP_ID_883444,Human_RBP_ID_1494644,Human_RBP_ID_2415649,Human_RBP_ID_3451188,Human_RBP_ID_8250207,Human_RBP_ID_9368955,Human_RBP_ID_12345295,Human_RBP_ID_26324699,Human_RBP_ID_26924746 Human_Splice_Rec_1513670,Human_Splice_Rec_1513671,Human_Splice_Rec_1513706,Human_Splice_Rec_1513707,Human_Splice_Rec_1513740,Human_Splice_Rec_1513741,Human_Splice_Rec_1513788 Clinvar_Rec_612 RMVar_hsa_circ_358622,RMVar_hsa_circ_24566,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 99850 RMVar_ID_99850 Human_SNP_ID_554976985 m1A Human chr14 - 50944403 50944403 50944403 CGCAGCCCGCCGCGCAGCCCGCCGCCCCAGCCATGGCGAAGCCCCTGACGGACCAGGAGAAGCGG CGCAGCCCGCCGCGCAGCCCGCCGCCCCAGCCTTGGCGAAGCCCCTGACGGACCAGGAGAAGCGG T A PYGL Ensembl:ENSG00000100504 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:50944285..50944486 26863410 MeRIP-seq:(Medium) rs1303715250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231560,Human_RBP_ID_446870,Human_RBP_ID_4294987,Human_RBP_ID_8404840,Human_RBP_ID_9368959 99851 RMVar_ID_99851 Human_SNP_ID_554977007 m1A Human chr14 - 50944432 50944432 50944432 GCGCCTCCGGCCGCACTTCCAGCTCTCTGCGCAGCCCGCCGCGCAGCCCGCCGCCCCAGCCATGG GCGCCTCCGGCCGCACTTCCAGCTCTCTGCGCCGCCCGCCGCGCAGCCCGCCGCCCCAGCCATGG T G PYGL Ensembl:ENSG00000100504 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,Starvation treatment;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:50944195..50944475;chr14:50944301..50944475;chr14:50944401..50944450;chr14:50944390..50944475;chr14:50944219..50944475;chr14:50944237..50944500 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs538311514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231560,Human_RBP_ID_446870,Human_RBP_ID_1275152,Human_RBP_ID_4308318,Human_RBP_ID_9368959 Clinvar_Rec_613,Clinvar_Rec_6048 99852 RMVar_ID_99852 Human_SNP_ID_554977017 m1A Human chr14 + 50944447 50944447 50944447 CGGGCTGCGCGGCGGGCTGCGCAGAGAGCTGGAAGTGCGGCCGGAGGCGCTGGGCTGCCGGGCAG CGGGCTGCGCGGCGGGCTGCGCAGAGAGCTGGGAGTGCGGCCGGAGGCGCTGGGCTGCCGGGCAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:50944326..50944475 26863196 MeRIP-seq:(Medium) rs747033305 Functional Loss SNV dbSNP153 33..33 33 - - - 99853 RMVar_ID_99853 Human_SNP_ID_554977018 m1A Human chr14 + 50944447 50944447 50944447 CGGGCTGCGCGGCGGGCTGCGCAGAGAGCTGGAAGTGCGGCCGGAGGCGCTGGGCTGCCGGGCAG CGGGCTGCGCGGCGGGCTGCGCAGAGAGCTGGTAGTGCGGCCGGAGGCGCTGGGCTGCCGGGCAG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:50944326..50944475 26863196 MeRIP-seq:(Medium) rs747033305 Functional Loss SNV dbSNP153 33..33 33 - - - 99854 RMVar_ID_99854 Human_SNP_ID_555047045 m1A Human chr14 - 51240302 51240302 51240302 CAGGACTGCCAGGGGAACTGCAAGACTCCCGGAGGGCGCCATTTCGCCGCTTGCCCACCTCACAG CAGGACTGCCAGGGGAACTGCAAGACTCCCGGTGGGCGCCATTTCGCCGCTTGCCCACCTCACAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:51240251..51240392;chr14:51240251..51240350 26863196 MeRIP-seq:(Medium) rs773212555 Functional Loss SNV dbSNP153 33..33 33 - - - 99855 RMVar_ID_99855 Human_SNP_ID_555047046 m1A Human chr14 - 51240302 51240302 51240302 CAGGACTGCCAGGGGAACTGCAAGACTCCCGGAGGGCGCCATTTCGCCGCTTGCCCACCTCACAG CAGGACTGCCAGGGGAACTGCAAGACTCCCGGGGGGCGCCATTTCGCCGCTTGCCCACCTCACAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:51240251..51240392;chr14:51240251..51240350 26863196 MeRIP-seq:(Medium) rs773212555 Functional Loss SNV dbSNP153 33..33 33 - - - 99856 RMVar_ID_99856 Human_SNP_ID_555047047 m1A Human chr14 - 51240302 51240302 51240302 CAGGACTGCCAGGGGAACTGCAAGACTCCCGGAGGGCGCCATTTCGCCGCTTGCCCACCTCACAG CAGGACTGCCAGGGGAACTGCAAGACTCCCGGCGGGCGCCATTTCGCCGCTTGCCCACCTCACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:51240251..51240392;chr14:51240251..51240350 26863196 MeRIP-seq:(Medium) rs773212555 Functional Loss SNV dbSNP153 33..33 33 - - - 99857 RMVar_ID_99857 Human_SNP_ID_555094239 m1A Human chr14 + 51436896 51436896 51436896 ATTAGAAGGTATTGATGAAGAAGGGGATGAGGATGAAGGTGAAGAAGAAGAAGATGATGATGAAG ATTAGAAGGTATTGATGAAGAAGGGGATGAGGGTGAAGGTGAAGAAGAAGAAGATGATGATGAAG A G SETP2 Ensembl:ENSG00000258893 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:51436867..51436935 26863196 MeRIP-seq:(Medium) rs937722408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8250647,Human_RBP_ID_17364264 99858 RMVar_ID_99858 Human_SNP_ID_555145242 m1A Human chr14 - 51651954 51651954 51651954 GTCTTGAGCACCAGGCGTTGGGCTCTCTGGTCACCCCTCTGACTCTTCCTACCGGCGCCGAGCCT GTCTTGAGCACCAGGCGTTGGGCTCTCTGGTCGCCCCTCTGACTCTTCCTACCGGCGCCGAGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:51651907..51651987 26863196 MeRIP-seq:(Medium) rs1163749529 Functional Loss SNV dbSNP153 33..33 33 - - - 99859 RMVar_ID_99859 Human_SNP_ID_555157652 m1A Human chr14 + 51704929 51704929 51704929 GGAAAATACTTCGAGCCAGAGGCTTACTTCCCATCTTGGGTAAGCACTGTTTTCAAATTCGAAAG GGAAAATACTTCGAGCCAGAGGCTTACTTCCCGTCTTGGGTAAGCACTGTTTTCAAATTCGAAAG A G FRMD6 Ensembl:ENSG00000139926 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:51704784..51708126 32194978 MeRIP-seq:(Medium) rs755751506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1514099,Human_Splice_Rec_1514141,Human_Splice_Rec_1514167,Human_Splice_Rec_1514193,Human_Splice_Rec_1514201,Human_Splice_Rec_1514219,Human_Splice_Rec_1514221 RMVar_hsa_circ_17375,RMVar_hsa_circ_314553,RMVar_hsa_circ_86907,RMVar_hsa_circ_122659,RMVar_hsa_circ_166613,RMVar_hsa_circ_166614,RMVar_hsa_circ_358729,RMVar_hsa_circ_369987,RMVar_hsa_circ_331328,RMVar_hsa_circ_322000,RMVar_hsa_circ_300957,RMVar_hsa_circ_282764,RMVar_hsa_circ_166616,RMVar_hsa_circ_166618,RMVar_hsa_circ_166619,RMVar_hsa_circ_166617,RMVar_hsa_circ_343069,RMVar_hsa_circ_166615,RMVar_hsa_circ_343981,RMVar_hsa_circ_50943,RMVar_hsa_circ_89917,RMVar_hsa_circ_4789,RMVar_hsa_circ_91393,RMVar_hsa_circ_266338,RMVar_hsa_circ_166625,RMVar_hsa_circ_166626 99860 RMVar_ID_99860 Human_SNP_ID_555223517 m1A Human chr14 + 51968368 51968366 51968368 CCTCTCTATTCGCTTTCTCCTGTTTTTTTTTTAAAAAAAAAGCATGAAAAAGGAAGAGAAAAAGT CCTCTCTATTCGCTTTCTCCTGTTTTTTTTT__AAAAAAAAGCATGAAAAAGGAAGAGAAAAAGT TTA T GNG2 Ensembl:ENSG00000186469 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1491543185 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18177536 99861 RMVar_ID_99861 Human_SNP_ID_555223519 m1A Human chr14 + 51968368 51968367 51968369 CCTCTCTATTCGCTTTCTCCTGTTTTTTTTTTAAAAAAAAAGCATGAAAAAGGAAGAGAAAAAGT CCTCTCTATTCGCTTTCTCCTGTTTTTTTTTT__AAAAAAAGCATGAAAAAGGAAGAGAAAAAGT TAA T GNG2 Ensembl:ENSG00000186469 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs72244277 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18177536 99862 RMVar_ID_99862 Human_SNP_ID_555223522 m1A Human chr14 + 51968368 51968368 51968368 CCTCTCTATTCGCTTTCTCCTGTTTTTTTTTTAAAAAAAAAGCATGAAAAAGGAAGAGAAAAAGT CCTCTCTATTCGCTTTCTCCTGTTTTTTTTTTTAAAAAAAAGCATGAAAAAGGAAGAGAAAAAGT A T GNG2 Ensembl:ENSG00000186469 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs8014838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18177536 99863 RMVar_ID_99863 Human_SNP_ID_555394107 m1A Human chr14 - 52640367 52640367 52640367 CCTTGGTAAATGCTGTACTCTTTGCATCAAGTATGCTAGTCATCCTTCCCCACTTGGAAAATTCC CCTTGGTAAATGCTGTACTCTTTGCATCAAGTGTGCTAGTCATCCTTCCCCACTTGGAAAATTCC T C ERO1A Ensembl:ENSG00000197930 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_447209,Human_RBP_ID_17248511,Human_RBP_ID_17481052,Human_RBP_ID_22385895,Human_RBP_ID_26428818 Human_miRNA_ID_1707018 GWAS_ID_13150 99864 RMVar_ID_99864 Human_SNP_ID_555406933 m1A Human chr14 - 52695757 52695757 52695757 CGGGCGCGGGCGCAGCGGACCGGGCGGGGCCGAGCCGGGAAGCTGGTCGGTGCGTCAGCCTCACG CGGGCGCGGGCGCAGCGGACCGGGCGGGGCCGCGCCGGGAAGCTGGTCGGTGCGTCAGCCTCACG T G ERO1A Ensembl:ENSG00000197930 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:52695712..52695925 26863196 MeRIP-seq:(Medium) rs866844253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231850,Human_RBP_ID_4307936,Human_RBP_ID_9352931,Human_RBP_ID_22438725 99865 RMVar_ID_99865 Human_SNP_ID_555410263 m1A Human chr14 + 52707259 52707257 52707259 ACCCTAGAGATAAGGCGCTTCAGGACTACCGCAAGAAGTTGCTTGAACACAAGGAGATCGACGGC ACCCTAGAGATAAGGCGCTTCAGGACTACCG__AGAAGTTGCTTGAACACAAGGAGATCGACGGC GCA G PSMC6 Ensembl:ENSG00000100519 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:52707201..52707342 26863196 MeRIP-seq:(Medium) rs748428557 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_756804,Human_RBP_ID_813049,Human_RBP_ID_1494954,Human_RBP_ID_1820151,Human_RBP_ID_4313042,Human_RBP_ID_5563242,Human_RBP_ID_12350118,Human_RBP_ID_17479284,Human_RBP_ID_18417967,Human_RBP_ID_18651720,Human_RBP_ID_23625499,Human_RBP_ID_26924886 Human_Splice_Rec_1514821,Human_Splice_Rec_1514827,Human_Splice_Rec_1514853,Human_Splice_Rec_1514865,Human_Splice_Rec_1514879,Human_Splice_Rec_1514905,Human_Splice_Rec_1514909,Human_Splice_Rec_1514929,Human_Splice_Rec_1514943,Human_Splice_Rec_1514955 Human_miRNA_ID_2742802 RMVar_hsa_circ_114848,RMVar_hsa_circ_166715 99866 RMVar_ID_99866 Human_SNP_ID_555410553 m1A Human chr14 + 52708387 52708387 52708387 AAATGATCTGAAGGCCCTACAGAGTGTTGGGCAGGTAGGTGATGGAGTTTGGGGAATAGGGGGTG AAATGATCTGAAGGCCCTACAGAGTGTTGGGCCGGTAGGTGATGGAGTTTGGGGAATAGGGGGTG A C PSMC6 Ensembl:ENSG00000100519 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:52708376..52708465 26863196 MeRIP-seq:(Medium) rs769435277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_881827,Human_RBP_ID_6356267,Human_RBP_ID_9345100,Human_RBP_ID_19065337,Human_RBP_ID_22439587,Human_RBP_ID_22649087,Human_RBP_ID_26325059 Human_Splice_Rec_1514822,Human_Splice_Rec_1514823,Human_Splice_Rec_1514828,Human_Splice_Rec_1514829,Human_Splice_Rec_1514866,Human_Splice_Rec_1514867,Human_Splice_Rec_1514880,Human_Splice_Rec_1514881,Human_Splice_Rec_1514906,Human_Splice_Rec_1514907,Human_Splice_Rec_1514910,Human_Splice_Rec_1514911,Human_Splice_Rec_1514918,Human_Splice_Rec_1514919,Human_Splice_Rec_1514930,Human_Splice_Rec_1514931,Human_Splice_Rec_1514956,Human_Splice_Rec_1514957,Human_Splice_Rec_1514974,Human_Splice_Rec_1514975,Human_Splice_Rec_1514978,Human_Splice_Rec_1514979 RMVar_hsa_circ_114848,RMVar_hsa_circ_166715,RMVar_hsa_circ_3353,RMVar_hsa_circ_365924,RMVar_hsa_circ_69753,RMVar_hsa_circ_1514 99867 RMVar_ID_99867 Human_SNP_ID_555415967 m1A Human chr14 + 52730246 52730246 52730246 CGGAGACTCTGGGGGAGGGAGACGGCAGCGGCATGGCGGCCGGGTGTAAGACGCCCGACCCTCCT CGGAGACTCTGGGGGAGGGAGACGGCAGCGGCGTGGCGGCCGGGTGTAAGACGCCCGACCCTCCT A G STYX Ensembl:ENSG00000198252 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:52730201..52730469 26863196 MeRIP-seq:(Medium) rs1225168322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231392,Human_RBP_ID_814179,Human_RBP_ID_18417968 RMVar_hsa_circ_110699,RMVar_hsa_circ_166719 99868 RMVar_ID_99868 Human_SNP_ID_555427570 m1A Human chr14 - 52775782 52775782 52775782 AGTTCCTGGGTTCAAGCCATCCCTCCTGCCTCAGCCTCCCCAGTAGCTGGAACTACAGGTGTGTG AGTTCCTGGGTTCAAGCCATCCCTCCTGCCTCCGCCTCCCCAGTAGCTGGAACTACAGGTGTGTG T G GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1490438517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1394737,Human_miRNA_ID_2367550,Human_miRNA_ID_2715172,Human_miRNA_ID_3015343,Human_miRNA_ID_3051154 RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 99869 RMVar_ID_99869 Human_SNP_ID_555429668 m1A Human chr14 - 52784664 52784664 52784664 AAAGTGACTTAATATTCAAATTTTTATTTTAGACCTTACTAGAAAAATGAAACCTGATGAAACTC AAAGTGACTTAATATTCAAATTTTTATTTTAGGCCTTACTAGAAAAATGAAACCTGATGAAACTC T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:52784580..52784708;chr14:52784551..52784724 26863196 MeRIP-seq:(Medium) rs892854613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308329,Human_RBP_ID_6356645,Human_RBP_ID_12351091 Human_Splice_Rec_1515046,Human_Splice_Rec_1515078 RMVar_hsa_circ_117524,RMVar_hsa_circ_166735,RMVar_hsa_circ_284431,RMVar_hsa_circ_297290 99870 RMVar_ID_99870 Human_SNP_ID_555431284 m1A Human chr14 - 52791455 52791455 52791455 CACTGGTGGGGGAGAGTCCGACGCGCCTGGCTAGGAGCGCCGACCGCAGGGCCTCTACGGGTGAG CACTGGTGGGGGAGAGTCCGACGCGCCTGGCTGGGAGCGCCGACCGCAGGGCCTCTACGGGTGAG T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:52784576..52791600 26863196 MeRIP-seq:(Medium) rs1210165133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231561,Human_RBP_ID_4307938,Human_RBP_ID_5352240,Human_RBP_ID_8941050,Human_RBP_ID_18417969,Human_RBP_ID_19065351,Human_RBP_ID_22439213 Human_Splice_Rec_1515045,Human_Splice_Rec_1515055,Human_Splice_Rec_1515067,Human_Splice_Rec_1515075 99871 RMVar_ID_99871 Human_SNP_ID_555431285 m1A Human chr14 + 52791460 52791460 52791460 CCGTAGAGGCCCTGCGGTCGGCGCTCCTAGCCAGGCGCGTCGGACTCTCCCCCACCAGTGTGCAC CCGTAGAGGCCCTGCGGTCGGCGCTCCTAGCCCGGCGCGTCGGACTCTCCCCCACCAGTGTGCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:52784646..52791603 26863196 MeRIP-seq:(Medium) rs996817762 Functional Loss SNV dbSNP153 33..33 33 - - - 99872 RMVar_ID_99872 Human_SNP_ID_555449090 m1A Human chr14 + 52858176 52858176 52858176 TTTCAATTCATGGCCCTAAGGAATGTGTGACAAATTCAAGTTTATTATATCATAACATGATAGAT TTTCAATTCATGGCCCTAAGGAATGTGTGACACATTCAAGTTTATTATATCATAACATGATAGAT A C AL139317.5 Ensembl:ENSG00000285664 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:52857964..52858213 32194978 MeRIP-seq:(Medium) rs182640915 Functional Loss SNV dbSNP153 33..33 33 - - - 99873 RMVar_ID_99873 Human_SNP_ID_555453218 m1A Human chr14 + 52874189 52874189 52874189 TCCCTCCTTTTTGTACTTACTTGAAAACTTTAATGTAGTCAGCAAGTTCAGGAATGGAAGTAATG TCCCTCCTTTTTGTACTTACTTGAAAACTTTATTGTAGTCAGCAAGTTCAGGAATGGAAGTAATG A T AL139317.5 Ensembl:ENSG00000285664 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:52864467..52874189 32194978 MeRIP-seq:(Medium) rs1014544620 Functional Loss SNV dbSNP153 33..33 33 - - - 99874 RMVar_ID_99874 Human_SNP_ID_555458142 m1A Human chr14 + 52893424 52893424 52893424 TCTTTAAGAGAGAAAGTTCTTCGGGGTGTCTGATATCTGTTAATAAAATAGATTGTTTTACTAGA TCTTTAAGAGAGAAAGTTCTTCGGGGTGTCTGGTATCTGTTAATAAAATAGATTGTTTTACTAGA A G AL139317.5 Ensembl:ENSG00000285664 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:52893401..52893450 26863196 MeRIP-seq:(Medium) rs1462517048 Functional Loss SNV dbSNP153 33..33 33 - - - 99875 RMVar_ID_99875 Human_SNP_ID_555464923 m1A Human chr14 - 52919309 52919309 52919309 GGTCTGACCATGCTCTCTGGTGGGAAAAGAAGAGAACTTGGCTTCTGAAGACACATTGGACCTTA GGTCTGACCATGCTCTCTGGTGGGAAAAGAAGGGAACTTGGCTTCTGAAGACACATTGGACCTTA T C FERMT2 Ensembl:ENSG00000073712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:52919258..52919392 26863196 MeRIP-seq:(Medium) rs758136365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1495038,Human_RBP_ID_1820241,Human_RBP_ID_4295545,Human_RBP_ID_9368969 Human_Splice_Rec_1515140,Human_Splice_Rec_1515200,Human_Splice_Rec_1515228,Human_Splice_Rec_1515284,Human_Splice_Rec_1515318,Human_Splice_Rec_1515356,Human_Splice_Rec_1515364,Human_Splice_Rec_1515370,Human_Splice_Rec_1515378 RMVar_hsa_circ_12267,RMVar_hsa_circ_63426,RMVar_hsa_circ_322574,RMVar_hsa_circ_345027 99876 RMVar_ID_99876 Human_SNP_ID_555473045 m1A Human chr14 - 52950997 52950997 52950997 CAGCGCTTCGCCAGCCGAGGAACCGGACGCGGACACCGCCGCCCCGCGAGCCTCCAGCCCCTCGC CAGCGCTTCGCCAGCCGAGGAACCGGACGCGGGCACCGCCGCCCCGCGAGCCTCCAGCCCCTCGC T C FERMT2 Ensembl:ENSG00000073712 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr14:52950880..52951021;chr14:52950951..52951025 26863196,32194978 MeRIP-seq:(Medium) rs1199276128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4295564,Human_RBP_ID_5257973,Human_RBP_ID_9370109 Human_Splice_Rec_1515197,Human_Splice_Rec_1515225,Human_Splice_Rec_1515315 Human_miRNA_ID_870944,Human_miRNA_ID_885213,Human_miRNA_ID_1394741,Human_miRNA_ID_2387001,Human_miRNA_ID_2388477,Human_miRNA_ID_2399624,Human_miRNA_ID_3030679,Human_miRNA_ID_3066014 RMVar_hsa_circ_88929,RMVar_hsa_circ_166749 99877 RMVar_ID_99877 Human_SNP_ID_555494711 m1A Human chr14 - 53041873 53041873 53041873 CCCCAACCTCCCCTCCACACATACACCTCTGTAATCTGATGCTTTAAGCTCAGATTAAAGCATCA CCCCAACCTCCCCTCCACACATACACCTCTGTTATCTGATGCTTTAAGCTCAGATTAAAGCATCA T A DDHD1 Ensembl:ENSG00000100523 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78389413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6356959 RMVar_hsa_circ_269123 99878 RMVar_ID_99878 Human_SNP_ID_555522504 m1A Human chr14 + 53152356 53152356 53152356 CGCACACAGGCTCGATGTTCACAAGCTCCACCATCTCCGGCTCGTGCCCCGTCGTACTCTGGCAG CGCACACAGGCTCGATGTTCACAAGCTCCACCGTCTCCGGCTCGTGCCCCGTCGTACTCTGGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:53152305..53152738 26863196 MeRIP-seq:(Medium) rs759392241 Functional Loss SNV dbSNP153 33..33 33 - - - 99879 RMVar_ID_99879 Human_SNP_ID_555522505 m1A Human chr14 + 53152356 53152356 53152356 CGCACACAGGCTCGATGTTCACAAGCTCCACCATCTCCGGCTCGTGCCCCGTCGTACTCTGGCAG CGCACACAGGCTCGATGTTCACAAGCTCCACCTTCTCCGGCTCGTGCCCCGTCGTACTCTGGCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:53152305..53152738 26863196 MeRIP-seq:(Medium) rs759392241 Functional Loss SNV dbSNP153 33..33 33 - - - 99880 RMVar_ID_99880 Human_SNP_ID_555522603 m1A Human chr14 - 53152542 53152542 53152542 CAAGAAGACCTGGAAGCCCTTCATCGGCTACGACTCGCTCCGCATCGAGCTCGCCTTCCGGACCC CAAGAAGACCTGGAAGCCCTTCATCGGCTACGGCTCGCTCCGCATCGAGCTCGCCTTCCGGACCC T C DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:53152492..53152660 26863196 MeRIP-seq:(Medium) rs1456862942 Functional Loss SNV dbSNP153 33..33 33 - - - 99881 RMVar_ID_99881 Human_SNP_ID_555522834 m1A Human chr14 + 53152905 53152905 53152905 GGTTGTGGTCGTCGGTGCCCGGCGCCAAATGCAGCCCGGGTTCCCCGCGCAGCAGGGCCAGGGGC GGTTGTGGTCGTCGGTGCCCGGCGCCAAATGCTGCCCGGGTTCCCCGCGCAGCAGGGCCAGGGGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:53152861..53152993 26863196 MeRIP-seq:(Medium) rs1343687328 Functional Loss SNV dbSNP153 33..33 33 - - - 99882 RMVar_ID_99882 Human_SNP_ID_555522966 m1A Human chr14 - 53153167 53153150 53153167 AGAAACTTCGGGTGGAGAGGGCGGCGGCGTTGAATGTGTGGCGGAAGCGCTGGGGGTCACGGCTC AGAAACTTCGGGTGGAGAGGGCGGCGGCGTTG_________________CTGGGGGTCACGGCTC GCGCTTCCGCCACACATT G DDHD1 Ensembl:ENSG00000100523 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr14:53153054..53153279;chr14:53153069..53153276 26863196 MeRIP-seq:(Medium) rs1487670020 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_231564,Human_RBP_ID_5522727,Human_RBP_ID_18418307,Human_RBP_ID_26325063 99883 RMVar_ID_99883 Human_SNP_ID_555823108 m1A Human chr14 - 54397047 54397047 54397047 ACCGGCTTCATCGCTGGCCGCCCCACGTCGAGACCAGTGCCGCCTCCCTCTGCAGCGCCGGCGAC ACCGGCTTCATCGCTGGCCGCCCCACGTCGAGCCCAGTGCCGCCTCCCTCTGCAGCGCCGGCGAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54396997..54399907 26863196 MeRIP-seq:(Medium) rs758333955 Functional Loss SNV dbSNP153 33..33 33 - - - 99884 RMVar_ID_99884 Human_SNP_ID_555823113 m1A Human chr14 + 54397052 54397052 54397052 CGGCGCTGCAGAGGGAGGCGGCACTGGTCTCGACGTGGGGCGGCCAGCGATGAAGCCGGTGAGTC CGGCGCTGCAGAGGGAGGCGGCACTGGTCTCGGCGTGGGGCGGCCAGCGATGAAGCCGGTGAGTC A G CDKN3 Ensembl:ENSG00000100526 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:54397001..54397140 26863196 MeRIP-seq:(Medium) rs1457362503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_447597,Human_RBP_ID_4295660 Human_Splice_Rec_1515851,Human_Splice_Rec_1515861,Human_Splice_Rec_1515875,Human_Splice_Rec_1515885,Human_Splice_Rec_1515897,Human_Splice_Rec_1515911,Human_Splice_Rec_1515927,Human_Splice_Rec_1515941 99885 RMVar_ID_99885 Human_SNP_ID_555826878 m1A Human chr14 - 54412558 54412558 54412558 ACCCATCTTCTTTTGTTTTAAACTTTCACACCAGCAGCTTGTGTTTTTATAGCCACTGACACACA ACCCATCTTCTTTTGTTTTAAACTTTCACACCTGCAGCTTGTGTTTTTATAGCCACTGACACACA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:54412556..54412757 26863196 MeRIP-seq:(Medium) rs955690498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6357764 99886 RMVar_ID_99886 Human_SNP_ID_555828060 m1A Human chr14 + 54417882 54417882 54417882 GCTGCTTGTCTCCTACTATACCTGTCTGACACAATATCACCAGAGCAAGCCATAGACAGCCTGCG GCTGCTTGTCTCCTACTATACCTGTCTGACACGATATCACCAGAGCAAGCCATAGACAGCCTGCG A G CDKN3 Ensembl:ENSG00000100526 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:54415876..54418244 32194978 MeRIP-seq:(Medium) rs1200441567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17248518,Human_RBP_ID_17651655,Human_RBP_ID_26808061 Human_Splice_Rec_1515860,Human_Splice_Rec_1515872,Human_Splice_Rec_1515873,Human_Splice_Rec_1515884,Human_Splice_Rec_1515894,Human_Splice_Rec_1515895,Human_Splice_Rec_1515908,Human_Splice_Rec_1515909,Human_Splice_Rec_1515922,Human_Splice_Rec_1515923,Human_Splice_Rec_1515938,Human_Splice_Rec_1515939,Human_Splice_Rec_1515956,Human_Splice_Rec_1515957,Human_Splice_Rec_1515968,Human_Splice_Rec_1515969,Human_Splice_Rec_1515978,Human_Splice_Rec_1515979 Human_miRNA_ID_2043407,Human_miRNA_ID_2045557,Human_miRNA_ID_2907987,Human_miRNA_ID_2930172,Human_miRNA_ID_3026825 RMVar_hsa_circ_26288,RMVar_hsa_circ_166765,RMVar_hsa_circ_370722 99887 RMVar_ID_99887 Human_SNP_ID_555830466 m1A Human chr14 - 54427833 54427833 54427833 TAACATCTTTTTTCTTCTTTTCAGCATGATCTATGTTTTGGTGAGCTCTTAGAACAACACACAGA TAACATCTTTTTTCTTCTTTTCAGCATGATCTTTGTTTTGGTGAGCTCTTAGAACAACACACAGA T A CNIH1 Ensembl:ENSG00000100528 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:54427775..54430191 32194978 MeRIP-seq:(Medium) rs763588082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883748,Human_RBP_ID_1495209,Human_RBP_ID_1820337,Human_RBP_ID_6357897,Human_RBP_ID_8794801,Human_RBP_ID_12354852,Human_RBP_ID_22758136,Human_RBP_ID_24410899 Human_Splice_Rec_1515988,Human_Splice_Rec_1515994,Human_Splice_Rec_1516000,Human_Splice_Rec_1516006,Human_Splice_Rec_1516016,Human_Splice_Rec_1516026 Human_miRNA_ID_2537901 RMVar_hsa_circ_97904,RMVar_hsa_circ_108220,RMVar_hsa_circ_166766,RMVar_hsa_circ_166767 99888 RMVar_ID_99888 Human_SNP_ID_555830467 m1A Human chr14 - 54427833 54427833 54427833 TAACATCTTTTTTCTTCTTTTCAGCATGATCTATGTTTTGGTGAGCTCTTAGAACAACACACAGA TAACATCTTTTTTCTTCTTTTCAGCATGATCTGTGTTTTGGTGAGCTCTTAGAACAACACACAGA T C CNIH1 Ensembl:ENSG00000100528 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:54427775..54430191 32194978 MeRIP-seq:(Medium) rs763588082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883748,Human_RBP_ID_1495209,Human_RBP_ID_1820337,Human_RBP_ID_6357897,Human_RBP_ID_8794801,Human_RBP_ID_12354852,Human_RBP_ID_22758136,Human_RBP_ID_24410899 Human_Splice_Rec_1515988,Human_Splice_Rec_1515994,Human_Splice_Rec_1516000,Human_Splice_Rec_1516006,Human_Splice_Rec_1516016,Human_Splice_Rec_1516026 Human_miRNA_ID_2537901 RMVar_hsa_circ_97904,RMVar_hsa_circ_108220,RMVar_hsa_circ_166766,RMVar_hsa_circ_166767 99889 RMVar_ID_99889 Human_SNP_ID_555832507 m1A Human chr14 + 54436674 54436674 54436674 TAAAATTTGGTATTACTGTAATAAATACCTTCAATTTTCAATTTCGTCAATGCCTCTGCTCAAGT TAAAATTTGGTATTACTGTAATAAATACCTTCGATTTTCAATTTCGTCAATGCCTCTGCTCAAGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:54436671..54441300 32194978 MeRIP-seq:(Medium) rs893887997 Functional Loss SNV dbSNP153 33..33 33 - - - 99890 RMVar_ID_99890 Human_SNP_ID_555833835 m1A Human chr14 - 54441318 54441318 54441318 CTCCCCGCTCCTCCTCCCCAGCCATGGCGTTCACGTTCGCGGCCTTCTGCTACATGCTGGCGCTG CTCCCCGCTCCTCCTCCCCAGCCATGGCGTTCGCGTTCGCGGCCTTCTGCTACATGCTGGCGCTG T C CNIH1 Ensembl:ENSG00000100528 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr14:54441180..54441350;chr14:54441251..54441381 26863196 MeRIP-seq:(Medium) rs1447385673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230996,Human_RBP_ID_447735,Human_RBP_ID_1495242,Human_RBP_ID_4295760,Human_RBP_ID_5493650,Human_RBP_ID_9323777,Human_RBP_ID_12355154,Human_RBP_ID_17363327,Human_RBP_ID_22439217,Human_RBP_ID_23626139,Human_RBP_ID_27227207 Human_Splice_Rec_1515981,Human_Splice_Rec_1515989,Human_Splice_Rec_1515995,Human_Splice_Rec_1516001,Human_Splice_Rec_1516007,Human_Splice_Rec_1516017,Human_Splice_Rec_1516027 RMVar_hsa_circ_86099,RMVar_hsa_circ_97904,RMVar_hsa_circ_166767,RMVar_hsa_circ_166771 99891 RMVar_ID_99891 Human_SNP_ID_555843879 m1A Human chr14 + 54483765 54483765 54483765 TCTTCGGCAACATCACAAACAACCAAAGACTCACTCTATAAAAGAAAAAAAACACACATAAAATG TCTTCGGCAACATCACAAACAACCAAAGACTCGCTCTATAAAAGAAAAAAAACACACATAAAATG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54483651..54483828 26863196 MeRIP-seq:(Medium) rs764131081 Functional Loss SNV dbSNP153 33..33 33 - - - 99892 RMVar_ID_99892 Human_SNP_ID_555845244 m1A Human chr14 + 54488976 54488976 54488976 AGCGGCCTGTCGCCTACACTCGGGCGCCTTTAAGAATGGCACGGCGGCCGCCTCCCTTCCTGCCC AGCGGCCTGTCGCCTACACTCGGGCGCCTTTAGGAATGGCACGGCGGCCGCCTCCCTTCCTGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:54488877..54489020;chr14:54488861..54489039 26863196 MeRIP-seq:(Medium) rs1179555060 Functional Loss SNV dbSNP153 33..33 33 - - - 99893 RMVar_ID_99893 Human_SNP_ID_555864090 m1A Human chr14 + 54566139 54566139 54566139 TCAGTCCTCCGCGAGCCGACACTGGAGGCAGCAGCAGCGGCGGCTGCAGCGGCCCCGACTCGAAG TCAGTCCTCCGCGAGCCGACACTGGAGGCAGCGGCAGCGGCGGCTGCAGCGGCCCCGACTCGAAG A G SAMD4A Ensembl:ENSG00000020577 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54566089..54566259 26863196 MeRIP-seq:(Medium) rs1467712659 Functional Loss SNV dbSNP153 33..33 33 - - - 99894 RMVar_ID_99894 Human_SNP_ID_555864639 m1A Human chr14 - 54567662 54567662 54567662 AGACAGTAGCACGGAAATGTTTCTTTAAAAAAAAAAACGACTTTTTAAAAATCCCCCACAAGGCA AGACAGTAGCACGGAAATGTTTCTTTAAAAAATAAAACGACTTTTTAAAAATCCCCCACAAGGCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54567626..54567771 26863196 MeRIP-seq:(Medium) rs888915235 Functional Loss SNV dbSNP153 33..33 33 - - - 99895 RMVar_ID_99895 Human_SNP_ID_555864640 m1A Human chr14 - 54567662 54567662 54567662 AGACAGTAGCACGGAAATGTTTCTTTAAAAAAAAAAACGACTTTTTAAAAATCCCCCACAAGGCA AGACAGTAGCACGGAAATGTTTCTTTAAAAAACAAAACGACTTTTTAAAAATCCCCCACAAGGCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54567626..54567771 26863196 MeRIP-seq:(Medium) rs888915235 Functional Loss SNV dbSNP153 33..33 33 - - - 99896 RMVar_ID_99896 Human_SNP_ID_555874180 m1A Human chr14 - 54607262 54607262 54607262 TTTTAAAATGAAAACCAAATCTACCTGCCACGATCTCACATGAGGAACTTCATTCCTCAGAGGGC TTTTAAAATGAAAACCAAATCTACCTGCCACGCTCTCACATGAGGAACTTCATTCCTCAGAGGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54607061..54607348 26863196 MeRIP-seq:(Medium) rs200452905 Functional Loss SNV dbSNP153 33..33 33 - - - 99897 RMVar_ID_99897 Human_SNP_ID_555894972 m1A Human chr14 - 54693860 54693860 54693860 TTTAAATTGCCCACCCCACTCTCTCACCTTACACTCCCTTATTCCCAGGTCATGCTTTGTTTTTT TTTAAATTGCCCACCCCACTCTCTCACCTTACGCTCCCTTATTCCCAGGTCATGCTTTGTTTTTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54693854..54694181 26863196 MeRIP-seq:(Medium) rs1026305677 Functional Loss SNV dbSNP153 33..33 33 - - - 99898 RMVar_ID_99898 Human_SNP_ID_555898426 m1A Human chr14 - 54708393 54708393 54708393 TCATATATCCCACTACCTACTCAGTATCTCCAACAGACATGCCAAACTCATCGTATATGACACTG TCATATATCCCACTACCTACTCAGTATCTCCATCAGACATGCCAAACTCATCGTATATGACACTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54708387..54708489 26863196 MeRIP-seq:(Medium) rs996323435 Functional Loss SNV dbSNP153 33..33 33 - - - 99899 RMVar_ID_99899 Human_SNP_ID_555918504 m1A Human chr14 - 54789061 54789060 54789061 CGCTCTCACAAAATCAAAACGGGAGAGGGACCAGGGGGAAAAAAGGCTGCAAAGTATCTTGGAGG CGCTCTCACAAAATCAAAACGGGAGAGGGACC_GGGGGAAAAAAGGCTGCAAAGTATCTTGGAGG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54789012..54789116 26863196 MeRIP-seq:(Medium) rs1387919309 Functional Loss DEL dbSNP153 33..33 33 - - - 99900 RMVar_ID_99900 Human_SNP_ID_555918505 m1A Human chr14 - 54789061 54789061 54789061 CGCTCTCACAAAATCAAAACGGGAGAGGGACCAGGGGGAAAAAAGGCTGCAAAGTATCTTGGAGG CGCTCTCACAAAATCAAAACGGGAGAGGGACCGGGGGGAAAAAAGGCTGCAAAGTATCTTGGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54789012..54789116 26863196 MeRIP-seq:(Medium) rs1461118381 Functional Loss SNV dbSNP153 33..33 33 - - - 99901 RMVar_ID_99901 Human_SNP_ID_555962219 m1A Human chr14 - 54961522 54961522 54961522 TAACAGTCAGCAAGGCAAAGGTGCATGGGAACAGGAGCAGAAGAGAAGCATTTGGGCTTAAGGAA TAACAGTCAGCAAGGCAAAGGTGCATGGGAACGGGAGCAGAAGAGAAGCATTTGGGCTTAAGGAA T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:54961400..54961755 26863196 MeRIP-seq:(Medium) rs949864061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12356364,Human_RBP_ID_23626624 RMVar_hsa_circ_8963,RMVar_hsa_circ_29698,RMVar_hsa_circ_81359,RMVar_hsa_circ_16601,RMVar_hsa_circ_109487,RMVar_hsa_circ_111610,RMVar_hsa_circ_166797,RMVar_hsa_circ_1018,RMVar_hsa_circ_302275,RMVar_hsa_circ_59289,RMVar_hsa_circ_166799,RMVar_hsa_circ_11903,RMVar_hsa_circ_346220,RMVar_hsa_circ_166798,RMVar_hsa_circ_345532,RMVar_hsa_circ_267068,RMVar_hsa_circ_166800,RMVar_hsa_circ_166802,RMVar_hsa_circ_50752,RMVar_hsa_circ_166801 99902 RMVar_ID_99902 Human_SNP_ID_555970164 m1A Human chr14 - 54991304 54991304 54991304 CAGCATTCACAATCTACCACTTGTAACATCCCAAAGGCCATTTTATGATGGACCCATGCCAACTC CAGCATTCACAATCTACCACTTGTAACATCCCGAAGGCCATTTTATGATGGACCCATGCCAACTC T C WDHD1 Ensembl:ENSG00000198554 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:54991224..54991375 32194978 MeRIP-seq:(Medium) rs775130952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1516420,Human_Splice_Rec_1516421,Human_Splice_Rec_1516466,Human_Splice_Rec_1516467,Human_Splice_Rec_1516493 RMVar_hsa_circ_765,RMVar_hsa_circ_29698,RMVar_hsa_circ_81359,RMVar_hsa_circ_109487,RMVar_hsa_circ_111610,RMVar_hsa_circ_166797,RMVar_hsa_circ_166799,RMVar_hsa_circ_166800,RMVar_hsa_circ_50752,RMVar_hsa_circ_67253,RMVar_hsa_circ_362896,RMVar_hsa_circ_304763,RMVar_hsa_circ_166810,RMVar_hsa_circ_309156,RMVar_hsa_circ_367329,RMVar_hsa_circ_307070,RMVar_hsa_circ_18515,RMVar_hsa_circ_277434,RMVar_hsa_circ_301397,RMVar_hsa_circ_166812,RMVar_hsa_circ_21512,RMVar_hsa_circ_51828,RMVar_hsa_circ_16848,RMVar_hsa_circ_374830,RMVar_hsa_circ_166811,RMVar_hsa_circ_166814,RMVar_hsa_circ_166816,RMVar_hsa_circ_101869,RMVar_hsa_circ_312036,RMVar_hsa_circ_166815 99903 RMVar_ID_99903 Human_SNP_ID_555985624 m1A Human chr14 + 55051708 55051708 55051708 CGCGCTGCTGGTGCTGTTGCCGCCGCTGCTCTAGCTGCCGTCAGTCAGGCTGCGCCCGCGTCTTC CGCGCTGCTGGTGCTGTTGCCGCCGCTGCTCTCGCTGCCGTCAGTCAGGCTGCGCCCGCGTCTTC A C MAPK1IP1L Ensembl:ENSG00000168175 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55051651..55051848 26863196 MeRIP-seq:(Medium) rs776678062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1495422,Human_RBP_ID_4296059,Human_RBP_ID_5315853,Human_RBP_ID_8405589,Human_RBP_ID_9323779,Human_RBP_ID_18418134,Human_RBP_ID_18652117,Human_RBP_ID_22044547,Human_RBP_ID_22439218,Human_RBP_ID_23626749,Human_RBP_ID_26925116,Human_RBP_ID_27227264 Human_Splice_Rec_1516537,Human_Splice_Rec_1516539,Human_Splice_Rec_1516545,Human_Splice_Rec_1516551 Human_miRNA_ID_2252653 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 99904 RMVar_ID_99904 Human_SNP_ID_555985625 m1A Human chr14 + 55051708 55051708 55051708 CGCGCTGCTGGTGCTGTTGCCGCCGCTGCTCTAGCTGCCGTCAGTCAGGCTGCGCCCGCGTCTTC CGCGCTGCTGGTGCTGTTGCCGCCGCTGCTCTGGCTGCCGTCAGTCAGGCTGCGCCCGCGTCTTC A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55051651..55051848 26863196 MeRIP-seq:(Medium) rs776678062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1495422,Human_RBP_ID_4296059,Human_RBP_ID_5315853,Human_RBP_ID_8405589,Human_RBP_ID_9323779,Human_RBP_ID_18418134,Human_RBP_ID_18652117,Human_RBP_ID_22044547,Human_RBP_ID_22439218,Human_RBP_ID_23626749,Human_RBP_ID_26925116,Human_RBP_ID_27227264 Human_Splice_Rec_1516537,Human_Splice_Rec_1516539,Human_Splice_Rec_1516545,Human_Splice_Rec_1516551 Human_miRNA_ID_2252653 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 99905 RMVar_ID_99905 Human_SNP_ID_555985688 m1A Human chr14 + 55051794 55051794 55051794 ATCGCCGCTTCTAGACCCTACTGCGGTCTCGGATATTGCCGGGTGAGGCTGCTTCGGTACTAGTG ATCGCCGCTTCTAGACCCTACTGCGGTCTCGGGTATTGCCGGGTGAGGCTGCTTCGGTACTAGTG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:55051676..55051892 26863196 MeRIP-seq:(Medium) rs949909063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_881853,Human_RBP_ID_998739,Human_RBP_ID_1495423,Human_RBP_ID_4308342,Human_RBP_ID_12357507,Human_RBP_ID_17363329,Human_RBP_ID_18652119,Human_RBP_ID_19064060,Human_RBP_ID_22044548 Human_Splice_Rec_1516537,Human_Splice_Rec_1516539,Human_Splice_Rec_1516545,Human_Splice_Rec_1516551 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 99906 RMVar_ID_99906 Human_SNP_ID_555985692 m1A Human chr14 - 55051805 55051805 55051805 TTCACGACTCCCACTAGTACCGAAGCAGCCTCACCCGGCAATATCCGAGACCGCAGTAGGGTCTA TTCACGACTCCCACTAGTACCGAAGCAGCCTCGCCCGGCAATATCCGAGACCGCAGTAGGGTCTA T C lnc-WDHD1-5 RNACentral:URS0000D58D4E lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:55051776..55051880 32194978 MeRIP-seq:(Medium) rs919306303 Functional Loss SNV dbSNP153 33..33 33 - - - 99907 RMVar_ID_99907 Human_SNP_ID_555988412 m1A Human chr14 - 55061677 55061677 55061677 CAACTTACCGAAAATTCATCAGACATTTTCCTAAAAAAAGAAAAGAAATGAAGGAAGAAAGAAAA CAACTTACCGAAAATTCATCAGACATTTTCCTTAAAAAAGAAAAGAAATGAAGGAAGAAAGAAAA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:55061676..55061725 26863196 MeRIP-seq:(Medium) rs1006974021 Functional Loss SNV dbSNP153 33..33 33 - - - 99908 RMVar_ID_99908 Human_SNP_ID_555988670 m1A Human chr14 - 55062734 55062734 55062734 CTTGGTGGGAGTCCAGATGGCACTGAAGATGGAGCACTCGGATTATTCCAAGGGTTGGAGCCTGG CTTGGTGGGAGTCCAGATGGCACTGAAGATGGGGCACTCGGATTATTCCAAGGGTTGGAGCCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55062684..55062941 26863196 MeRIP-seq:(Medium) rs746576793 Functional Loss SNV dbSNP153 33..33 33 - - - 99909 RMVar_ID_99909 Human_SNP_ID_555988671 m1A Human chr14 - 55062734 55062734 55062734 CTTGGTGGGAGTCCAGATGGCACTGAAGATGGAGCACTCGGATTATTCCAAGGGTTGGAGCCTGG CTTGGTGGGAGTCCAGATGGCACTGAAGATGGCGCACTCGGATTATTCCAAGGGTTGGAGCCTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55062684..55062941 26863196 MeRIP-seq:(Medium) rs746576793 Functional Loss SNV dbSNP153 33..33 33 - - - 99910 RMVar_ID_99910 Human_SNP_ID_555988719 m1A Human chr14 + 55062854 55062854 55062854 GTGCCTCCCACCGGACCACCTCCAGGACCCCCAGCACCCTTTCCTCCTTCCGGACCATCATGTCC GTGCCTCCCACCGGACCACCTCCAGGACCCCCGGCACCCTTTCCTCCTTCCGGACCATCATGTCC A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:55062676..55062950 26863196 MeRIP-seq:(Medium) rs140511390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231297,Human_RBP_ID_5127692,Human_RBP_ID_12358014,Human_RBP_ID_17076472,Human_RBP_ID_17363332,Human_RBP_ID_18937314,Human_RBP_ID_22044550,Human_RBP_ID_27227266,Human_RBP_ID_27431663 Human_miRNA_ID_2685126,Human_miRNA_ID_3078185 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826,RMVar_hsa_circ_305079 99911 RMVar_ID_99911 Human_SNP_ID_556006704 m1A Human chr14 - 55137386 55137386 55137386 GGGAAGAAACAGGCATAAAACACTTACCGAAAAATTGTCTGCCATTTTCCTGAAAGAAACAAAGA GGGAAGAAACAGGCATAAAACACTTACCGAAACATTGTCTGCCATTTTCCTGAAAGAAACAAAGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:55137351..55137400 26863196 MeRIP-seq:(Medium) rs770465937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3452748 99912 RMVar_ID_99912 Human_SNP_ID_556007470 m1A Human chr14 + 55140354 55140354 55140354 GCTGATAACAATTCTGGGCACGGTGAAGCCCAATGCAAACAGGTAAGGAGAGCAAAATTAACAAG GCTGATAACAATTCTGGGCACGGTGAAGCCCAGTGCAAACAGGTAAGGAGAGCAAAATTAACAAG A G LGALS3 Ensembl:ENSG00000131981 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:55140276..55140375 32194978 MeRIP-seq:(Medium) rs772155739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1516566,Human_Splice_Rec_1516567,Human_Splice_Rec_1516574,Human_Splice_Rec_1516575,Human_Splice_Rec_1516582,Human_Splice_Rec_1516583,Human_Splice_Rec_1516588,Human_Splice_Rec_1516589,Human_Splice_Rec_1516598,Human_Splice_Rec_1516599,Human_Splice_Rec_1516602 RMVar_hsa_circ_4779 99913 RMVar_ID_99913 Human_SNP_ID_556020976 m1A Human chr14 - 55189153 55189153 55189153 GACAGGATGTCTTCATCACATTTTGCCAGTCGACACAGGAAGGATATAAGTACTGAAATGATTAG GACAGGATGTCTTCATCACATTTTGCCAGTCGGCACAGGAAGGATATAAGTACTGAAATGATTAG T C DLGAP5 Ensembl:ENSG00000126787 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:55189102..55191095 26863196 MeRIP-seq:(Medium) rs770813720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2417016,Human_RBP_ID_6359919,Human_RBP_ID_12358982,Human_RBP_ID_18652218,Human_RBP_ID_22438502,Human_RBP_ID_22578375 Human_Splice_Rec_1516604,Human_Splice_Rec_1516642,Human_Splice_Rec_1516682,Human_Splice_Rec_1516694 RMVar_hsa_circ_62580,RMVar_hsa_circ_36398,RMVar_hsa_circ_5558,RMVar_hsa_circ_21569,RMVar_hsa_circ_90076,RMVar_hsa_circ_166830 99914 RMVar_ID_99914 Human_SNP_ID_556020979 m1A Human chr14 - 55189158 55189158 55189158 TCCTTGACAGGATGTCTTCATCACATTTTGCCAGTCGACACAGGAAGGATATAAGTACTGAAATG TCCTTGACAGGATGTCTTCATCACATTTTGCCGGTCGACACAGGAAGGATATAAGTACTGAAATG T C DLGAP5 Ensembl:ENSG00000126787 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55189108..55189230 26863196 MeRIP-seq:(Medium) rs1391005993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_883009,Human_RBP_ID_2417016,Human_RBP_ID_6359919,Human_RBP_ID_12358984,Human_RBP_ID_18652218,Human_RBP_ID_22438502,Human_RBP_ID_22578375 Human_Splice_Rec_1516604,Human_Splice_Rec_1516642,Human_Splice_Rec_1516682,Human_Splice_Rec_1516694 RMVar_hsa_circ_62580,RMVar_hsa_circ_36398,RMVar_hsa_circ_5558,RMVar_hsa_circ_21569,RMVar_hsa_circ_90076,RMVar_hsa_circ_166830 99915 RMVar_ID_99915 Human_SNP_ID_556021614 m1A Human chr14 - 55191538 55191538 55191538 GGAGGCTCGGGTTGTGAGGGTTCCTGCTTCGGAGTCGGCGGTGGTCGTCCAGACCGAGTGTTCTT GGAGGCTCGGGTTGTGAGGGTTCCTGCTTCGGGGTCGGCGGTGGTCGTCCAGACCGAGTGTTCTT T C DLGAP5 Ensembl:ENSG00000126787 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:55191457..55191583 26863196 MeRIP-seq:(Medium) rs986096058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758329,Human_RBP_ID_4296239,Human_RBP_ID_9282178,Human_RBP_ID_22438504,Human_RBP_ID_22924040,Human_RBP_ID_23626934 Human_Splice_Rec_1516603,Human_Splice_Rec_1516641,Human_Splice_Rec_1516691 99916 RMVar_ID_99916 Human_SNP_ID_556042031 m1A Human chr14 + 55271435 55271435 55271435 CGCCGCGCCGCGCTGGGTGCTCGGTCCGACTCAGCGGTGGGGAGTGAGCCAGGCCTCCCGCCACC CGCCGCGCCGCGCTGGGTGCTCGGTCCGACTCTGCGGTGGGGAGTGAGCCAGGCCTCCCGCCACC A T FBXO34 Ensembl:ENSG00000178974 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:55271425..55271666 26863196 MeRIP-seq:(Medium) rs1202659167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308344,Human_RBP_ID_26778069 RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 99917 RMVar_ID_99917 Human_SNP_ID_556042040 m1A Human chr14 + 55271453 55271453 55271453 GCTCGGTCCGACTCAGCGGTGGGGAGTGAGCCAGGCCTCCCGCCACCGCTGCTGCCGCCACCACT GCTCGGTCCGACTCAGCGGTGGGGAGTGAGCCGGGCCTCCCGCCACCGCTGCTGCCGCCACCACT A G FBXO34 Ensembl:ENSG00000178974 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55271410..55272168 26863196 MeRIP-seq:(Medium) rs1325306371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4296259,Human_RBP_ID_26778069 Human_Splice_Rec_1516705,Human_Splice_Rec_1516707 RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 99918 RMVar_ID_99918 Human_SNP_ID_556042043 m1A Human chr14 - 55271458 55271458 55271458 GACGCAGTGGTGGCGGCAGCAGCGGTGGCGGGAGGCCTGGCTCACTCCCCACCGCTGAGTCGGAC GACGCAGTGGTGGCGGCAGCAGCGGTGGCGGGGGGCCTGGCTCACTCCCCACCGCTGAGTCGGAC T C AL158801.2 Ensembl:ENSG00000258413 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55271412..55271592 26863196 MeRIP-seq:(Medium) rs1397648480 Functional Loss SNV dbSNP153 33..33 33 - - - 99919 RMVar_ID_99919 Human_SNP_ID_556042044 m1A Human chr14 - 55271458 55271458 55271458 GACGCAGTGGTGGCGGCAGCAGCGGTGGCGGGAGGCCTGGCTCACTCCCCACCGCTGAGTCGGAC GACGCAGTGGTGGCGGCAGCAGCGGTGGCGGGCGGCCTGGCTCACTCCCCACCGCTGAGTCGGAC T G AL158801.2 Ensembl:ENSG00000258413 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55271412..55271592 26863196 MeRIP-seq:(Medium) rs1397648480 Functional Loss SNV dbSNP153 33..33 33 - - - 99920 RMVar_ID_99920 Human_SNP_ID_556042119 m1A Human chr14 + 55271699 55271699 55271699 GGGGGCGGGGGCGCCGCCCGCGGGTCCGGGGTAGGGACCCGGCCGCCTGCGCCTCCTCCGGTGCG GGGGGCGGGGGCGCCGCCCGCGGGTCCGGGGTGGGGACCCGGCCGCCTGCGCCTCCTCCGGTGCG A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:55271432..55271741 26863196 MeRIP-seq:(Medium) rs1343922006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5353074,Human_RBP_ID_9324049,Human_RBP_ID_9417889,Human_RBP_ID_18457828,Human_RBP_ID_18936766,Human_RBP_ID_26778070 RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 99921 RMVar_ID_99921 Human_SNP_ID_556122594 m1A Human chr14 + 55580042 55580042 55580042 TCGGCCCAGCTGGGGGACGCGGTCTCGGGAAGAAAGCCCGGAATCCCGAGCCGGCCAGCCGCGAG TCGGCCCAGCTGGGGGACGCGGTCTCGGGAAGGAAGCCCGGAATCCCGAGCCGGCCAGCCGCGAG A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55579991..55580072 26863196 MeRIP-seq:(Medium) rs1006940126 Functional Loss SNV dbSNP153 33..33 33 - - - 99922 RMVar_ID_99922 Human_SNP_ID_556122735 m1A Human chr14 + 55580287 55580287 55580287 CGGCGGCGGCGGCGGCGGCGGCGGCGCCTCGGAGCGGGCGGCCCGGGCTGTAGTGCCGGCGCCGC CGGCGGCGGCGGCGGCGGCGGCGGCGCCTCGGGGCGGGCGGCCCGGGCTGTAGTGCCGGCGCCGC A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55580249..55580424 26863196 MeRIP-seq:(Medium) rs1230379743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4307953,Human_RBP_ID_8797836,Human_RBP_ID_9323782 Human_Splice_Rec_1516809,Human_Splice_Rec_1516895,Human_Splice_Rec_1516905,Human_Splice_Rec_1516911,Human_Splice_Rec_1516993,Human_Splice_Rec_1517083 RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 99923 RMVar_ID_99923 Human_SNP_ID_556122995 m1A Human chr14 + 55580838 55580838 55580838 CTCCGGCGGCGTCCCCGGGCCGGAGCTGGGCCACACTTACGCCATGCTGGAGTTCCAGTCCTCGC CTCCGGCGGCGTCCCCGGGCCGGAGCTGGGCCGCACTTACGCCATGCTGGAGTTCCAGTCCTCGC A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:55580833..55581034 26863196 MeRIP-seq:(Medium) rs932103665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 99924 RMVar_ID_99924 Human_SNP_ID_556131197 m1A Human chr14 + 55612404 55612404 55612404 AAGTAGTGTTAGGGAAAGAAAAAAGAAGGAAAAGAAACAAAAGCCTGTGCTTGAAGAGCAGGTCA AAGTAGTGTTAGGGAAAGAAAAAAGAAGGAAAGGAAACAAAAGCCTGTGCTTGAAGAGCAGGTCA A G KTN1 Ensembl:ENSG00000126777 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55612353..55612503 26863196 MeRIP-seq:(Medium) rs1455243672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120173,Human_RBP_ID_1820765,Human_RBP_ID_17187308 Human_miRNA_ID_834479,Human_miRNA_ID_2359982 RMVar_hsa_circ_16694,RMVar_hsa_circ_266361,RMVar_hsa_circ_269272,RMVar_hsa_circ_53501,RMVar_hsa_circ_276588,RMVar_hsa_circ_336962,RMVar_hsa_circ_359358,RMVar_hsa_circ_334204,RMVar_hsa_circ_72947,RMVar_hsa_circ_45494,RMVar_hsa_circ_166840,RMVar_hsa_circ_166842,RMVar_hsa_circ_5842,RMVar_hsa_circ_166843,RMVar_hsa_circ_166841 99925 RMVar_ID_99925 Human_SNP_ID_556131205 m1A Human chr14 + 55612431 55612431 55612431 GGAAAAGAAACAAAAGCCTGTGCTTGAAGAGCAGGTCATCAAAGAAAGTGACGCATCAAAGATTC GGAAAAGAAACAAAAGCCTGTGCTTGAAGAGCGGGTCATCAAAGAAAGTGACGCATCAAAGATTC A G KTN1 Ensembl:ENSG00000126777 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:55612381..55612489 26863196 MeRIP-seq:(Medium) rs1042339266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120173,Human_RBP_ID_22924054 RMVar_hsa_circ_16694,RMVar_hsa_circ_266361,RMVar_hsa_circ_269272,RMVar_hsa_circ_53501,RMVar_hsa_circ_276588,RMVar_hsa_circ_336962,RMVar_hsa_circ_359358,RMVar_hsa_circ_334204,RMVar_hsa_circ_72947,RMVar_hsa_circ_45494,RMVar_hsa_circ_166840,RMVar_hsa_circ_166842,RMVar_hsa_circ_5842,RMVar_hsa_circ_166843,RMVar_hsa_circ_166841 99926 RMVar_ID_99926 Human_SNP_ID_556135360 m1A Human chr14 + 55628003 55628003 55628003 CGCTGCTGTGAAGGAAGATGCTGCTGCTACAAAGGATCGGTGTAAGCAGTTAACCCAGGTGAAGA CGCTGCTGTGAAGGAAGATGCTGCTGCTACAAGGGATCGGTGTAAGCAGTTAACCCAGGTGAAGA A G KTN1 Ensembl:ENSG00000126777 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:55627954..55628076;chr14:55627901..55628050 26863196 MeRIP-seq:(Medium) rs147823515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758328,Human_RBP_ID_8230510,Human_RBP_ID_9369003,Human_RBP_ID_22044802,Human_RBP_ID_26325081 Human_Splice_Rec_1516818,Human_Splice_Rec_1516819,Human_Splice_Rec_1516896,Human_Splice_Rec_1516897,Human_Splice_Rec_1516920,Human_Splice_Rec_1516921,Human_Splice_Rec_1517004,Human_Splice_Rec_1517005,Human_Splice_Rec_1517094,Human_Splice_Rec_1517095,Human_Splice_Rec_1517176,Human_Splice_Rec_1517177,Human_Splice_Rec_1517256,Human_Splice_Rec_1517257,Human_Splice_Rec_1517336,Human_Splice_Rec_1517337 RMVar_hsa_circ_9339,RMVar_hsa_circ_53501,RMVar_hsa_circ_359358,RMVar_hsa_circ_334204,RMVar_hsa_circ_72947,RMVar_hsa_circ_45494,RMVar_hsa_circ_166840,RMVar_hsa_circ_5842,RMVar_hsa_circ_166841,RMVar_hsa_circ_72886,RMVar_hsa_circ_308881,RMVar_hsa_circ_352193,RMVar_hsa_circ_307402,RMVar_hsa_circ_72887,RMVar_hsa_circ_166845,RMVar_hsa_circ_48173,RMVar_hsa_circ_52123,RMVar_hsa_circ_267966 99927 RMVar_ID_99927 Human_SNP_ID_556135362 m1A Human chr14 - 55628007 55628007 55628007 AATGTCTTCACCTGGGTTAACTGCTTACACCGATCCTTTGTAGCAGCAGCATCTTCCTTCACAGC AATGTCTTCACCTGGGTTAACTGCTTACACCGCTCCTTTGTAGCAGCAGCATCTTCCTTCACAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55627958..55628070 26863196 MeRIP-seq:(Medium) rs141376736 Functional Loss SNV dbSNP153 33..33 33 - - - 99928 RMVar_ID_99928 Human_SNP_ID_556257620 m1A Human chr14 + 56118475 56118475 56118475 CGCGGCGCGCGGAGCTCCGGGGAGTCAGGCGGAGCAGCCGCGCAGCCACGACGGAGCAGCAGCGG CGCGGCGCGCGGAGCTCCGGGGAGTCAGGCGGGGCAGCCGCGCAGCCACGACGGAGCAGCAGCGG A G PELI2 Ensembl:ENSG00000139946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:56118427..56118546;chr14:56118344..56118550 26863196 MeRIP-seq:(Medium) rs1007935136 Functional Loss SNV dbSNP153 33..33 33 - - - 99929 RMVar_ID_99929 Human_SNP_ID_556257679 m1A Human chr14 - 56118628 56118617 56118629 GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGACGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT GGAGCCCCGCTCGGCCGCCGACGCCGCCGCC____________TCCGCCGCGATCCCCGCCGAGT AGGCGGCGGCGTC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56118370..56118656 26863196 MeRIP-seq:(Medium) rs3832944 Functional Loss DEL dbSNP153 32..43 33 - - - 99930 RMVar_ID_99930 Human_SNP_ID_556257687 m1A Human chr14 - 56118628 56118619 56118628 GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGACGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCG_________CCTCCGCCGCGATCCCCGCCGAGT GCGGCGGCGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56118370..56118656 26863196 MeRIP-seq:(Medium) rs1232284060 Functional Loss DEL dbSNP153 33..41 33 - - - 99931 RMVar_ID_99931 Human_SNP_ID_556257691 m1A Human chr14 - 56118628 56118625 56118628 GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGACGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCG___CCGCCGCCTCCGCCGCGATCCCCGCCGAGT GCGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56118370..56118656 26863196 MeRIP-seq:(Medium) rs747429977 Functional Loss DEL dbSNP153 33..35 33 - - - 99932 RMVar_ID_99932 Human_SNP_ID_556257694 m1A Human chr14 - 56118628 56118628 56118628 GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGACGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGCCGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56118370..56118656 26863196 MeRIP-seq:(Medium) rs531124616 Functional Loss SNV dbSNP153 33..33 33 - - - 99933 RMVar_ID_99933 Human_SNP_ID_556373286 m1A Human chr14 + 56579949 56579948 56579949 GAGTCCCCATGGCGACGGCAGGGGCCAGGCCCAGGGGCGGGCAGTCCGAGTGGGGCTGCGGCGCT GAGTCCCCATGGCGACGGCAGGGGCCAGGCCC_GGGGCGGGCAGTCCGAGTGGGGCTGCGGCGCT CA C TMEM260 Ensembl:ENSG00000070269 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:56579905..56580005 26863196 MeRIP-seq:(Medium) rs1340644609 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_231499,Human_RBP_ID_4308837 99934 RMVar_ID_99934 Human_SNP_ID_556374298 m1A Human chr14 + 56583694 56583694 56583694 TGGGGAGGCTGGGGAAGCAGGTGTCTAAGGAAAGGTTACCAAGAAGGTGGCAATTGAACTTGGCC TGGGGAGGCTGGGGAAGCAGGTGTCTAAGGAAGGGTTACCAAGAAGGTGGCAATTGAACTTGGCC A G TMEM260 Ensembl:ENSG00000070269 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56583689..56583799 26863196 MeRIP-seq:(Medium) rs575978963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6361584 99935 RMVar_ID_99935 Human_SNP_ID_556545200 m1A Human chr14 - 57268816 57268816 57268816 AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCATGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCTTGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG T A EXOC5 Ensembl:ENSG00000070367 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:57268776..57268850 26863196 MeRIP-seq:(Medium) rs547676439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_448512,Human_RBP_ID_4308350,Human_RBP_ID_8798110,Human_RBP_ID_22044561,Human_RBP_ID_23118310 99936 RMVar_ID_99936 Human_SNP_ID_556545201 m1A Human chr14 - 57268816 57268816 57268816 AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCATGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCGTGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG T C EXOC5 Ensembl:ENSG00000070367 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:57268776..57268850 26863196 MeRIP-seq:(Medium) rs547676439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_448512,Human_RBP_ID_4308350,Human_RBP_ID_8798110,Human_RBP_ID_22044561,Human_RBP_ID_23118310 99937 RMVar_ID_99937 Human_SNP_ID_556545202 m1A Human chr14 - 57268816 57268816 57268816 AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCATGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG AGGCAGCTGACAAGCGTTTGCGGCTTCGCTTCCTGGCCGCTCTCCCGCCCCTCCTGGGATCTGTG T G EXOC5 Ensembl:ENSG00000070367 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:57268776..57268850 26863196 MeRIP-seq:(Medium) rs547676439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_448512,Human_RBP_ID_4308350,Human_RBP_ID_8798110,Human_RBP_ID_22044561,Human_RBP_ID_23118310 99938 RMVar_ID_99938 Human_SNP_ID_556546924 m1A Human chr14 + 57275445 57275429 57275445 AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGAAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG AGAGAGAGGAGAGAGAG________________AGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG GAGAGAGAGAAGAGAGA G AP5M1 Ensembl:ENSG00000053770 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:57275395..57275489 26863196 MeRIP-seq:(Medium) rs1290847093 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_812725 RMVar_hsa_circ_84624,RMVar_hsa_circ_32603,RMVar_hsa_circ_63824,RMVar_hsa_circ_166888,RMVar_hsa_circ_302965,RMVar_hsa_circ_269906,RMVar_hsa_circ_166890,RMVar_hsa_circ_4509,RMVar_hsa_circ_166891 99939 RMVar_ID_99939 Human_SNP_ID_556546926 m1A Human chr14 + 57275445 57275431 57275445 AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGAAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG AGAGAGAGGAGAGAGAGAG______________AGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG GAGAGAGAAGAGAGA G AP5M1 Ensembl:ENSG00000053770 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:57275395..57275489 26863196 MeRIP-seq:(Medium) rs1178002474 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_812725 RMVar_hsa_circ_84624,RMVar_hsa_circ_32603,RMVar_hsa_circ_63824,RMVar_hsa_circ_166888,RMVar_hsa_circ_302965,RMVar_hsa_circ_269906,RMVar_hsa_circ_166890,RMVar_hsa_circ_4509,RMVar_hsa_circ_166891 99940 RMVar_ID_99940 Human_SNP_ID_556546927 m1A Human chr14 + 57275445 57275431 57275445 AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGAAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG AGAGAGAGGAGAGAGAGAGAGAGAGA_______AGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG GAGAGAGAAGAGAGA GAGAGAGA AP5M1 Ensembl:ENSG00000053770 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:57275395..57275489 26863196 MeRIP-seq:(Medium) rs1178002474 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_812725 RMVar_hsa_circ_84624,RMVar_hsa_circ_32603,RMVar_hsa_circ_63824,RMVar_hsa_circ_166888,RMVar_hsa_circ_302965,RMVar_hsa_circ_269906,RMVar_hsa_circ_166890,RMVar_hsa_circ_4509,RMVar_hsa_circ_166891 99941 RMVar_ID_99941 Human_SNP_ID_556546931 m1A Human chr14 + 57275445 57275437 57275446 AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGAAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG AGAGAGAGGAGAGAGAGAGAGAGAG_________GAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG GAAGAGAGAA G AP5M1 Ensembl:ENSG00000053770 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:57275395..57275489 26863196 MeRIP-seq:(Medium) rs1055156239 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_812725 RMVar_hsa_circ_84624,RMVar_hsa_circ_32603,RMVar_hsa_circ_63824,RMVar_hsa_circ_166888,RMVar_hsa_circ_302965,RMVar_hsa_circ_269906,RMVar_hsa_circ_166890,RMVar_hsa_circ_4509,RMVar_hsa_circ_166891 99942 RMVar_ID_99942 Human_SNP_ID_556546935 m1A Human chr14 + 57275445 57275445 57275445 AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGAAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG AGAGAGAGGAGAGAGAGAGAGAGAGAAGAGAGGAGAGAGAGAAGAGAGAAGAGAAAAGAGAGAGG A G AP5M1 Ensembl:ENSG00000053770 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:57275395..57275489 26863196 MeRIP-seq:(Medium) rs1285315383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812725 RMVar_hsa_circ_84624,RMVar_hsa_circ_32603,RMVar_hsa_circ_63824,RMVar_hsa_circ_166888,RMVar_hsa_circ_302965,RMVar_hsa_circ_269906,RMVar_hsa_circ_166890,RMVar_hsa_circ_4509,RMVar_hsa_circ_166891 99943 RMVar_ID_99943 Human_SNP_ID_556574925 m1A Human chr14 + 57390643 57390622 57390643 CTTGGCGGCTGTGGAGGCTGCCGCGGCTGCGAAGGAGGCGGCGGCGGTGGCGGAGGAAGAGGAGT CTTGGCGGCTGT_____________________GGAGGCGGCGGCGGTGGCGGAGGAAGAGGAGT TGGAGGCTGCCGCGGCTGCGAA T NAA30 Ensembl:ENSG00000139977 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:57390576..57391388;chr14:57390576..57391315;chr14:57390576..57391342 26863196 MeRIP-seq:(Medium) rs1475777738 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_4307957 Human_Splice_Rec_1518439,Human_Splice_Rec_1518445,Human_Splice_Rec_1518453 99944 RMVar_ID_99944 Human_SNP_ID_556779480 m1A Human chr14 + 58200202 58200202 58200202 GTTGGCCGCGGAGACTGCGACCCTCTTCTCTCAGTCTGCCTTACTACCATGCCGCTCTACGAGGG GTTGGCCGCGGAGACTGCGACCCTCTTCTCTCGGTCTGCCTTACTACCATGCCGCTCTACGAGGG A G ACTR10 Ensembl:ENSG00000131966 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:58200151..58200300 26863196 MeRIP-seq:(Medium) rs779564612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308351,Human_RBP_ID_9282181 Human_Splice_Rec_1518675,Human_Splice_Rec_1518699,Human_Splice_Rec_1518723,Human_Splice_Rec_1518737,Human_Splice_Rec_1518759,Human_Splice_Rec_1518771,Human_Splice_Rec_1518777,Human_Splice_Rec_1518785 RMVar_hsa_circ_113384,RMVar_hsa_circ_166907 99945 RMVar_ID_99945 Human_SNP_ID_556779526 m1A Human chr14 + 58200293 58200293 58200293 CGGTCGTGATCGACCTGGGAGAGGCCTTTACCAAGTGAGTGGCCGTGACGCCAGCTGTGTTCGAC CGGTCGTGATCGACCTGGGAGAGGCCTTTACCGAGTGAGTGGCCGTGACGCCAGCTGTGTTCGAC A G ACTR10 Ensembl:ENSG00000131966 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:58200233..58200336 26863410 MeRIP-seq:(Medium) rs996865668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308351,Human_RBP_ID_18980655,Human_RBP_ID_19064067 Human_Splice_Rec_1518675,Human_Splice_Rec_1518699,Human_Splice_Rec_1518723,Human_Splice_Rec_1518737,Human_Splice_Rec_1518759,Human_Splice_Rec_1518771,Human_Splice_Rec_1518777,Human_Splice_Rec_1518785 RMVar_hsa_circ_113384,RMVar_hsa_circ_166907 99946 RMVar_ID_99946 Human_SNP_ID_556789421 m1A Human chr14 - 58239910 58239910 58239910 ATGGGACTCTTAATCCCAGGGTCGTGGGTTCGAGCCCCACGTTGGGCGCGGGTTGTAACTTTTTT ATGGGACTCTTAATCCCAGGGTCGTGGGTTCGGGCCCCACGTTGGGCGCGGGTTGTAACTTTTTT T C ARMH4 Ensembl:ENSG00000139971 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs537455542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41050,Human_RBP_ID_122422,Human_RBP_ID_1172425,Human_RBP_ID_1495966,Human_RBP_ID_1821078,Human_RBP_ID_3453813,Human_RBP_ID_4313308,Human_RBP_ID_5274430,Human_RBP_ID_5439142,Human_RBP_ID_6363136,Human_RBP_ID_8250226,Human_RBP_ID_8406080,Human_RBP_ID_9769891,Human_RBP_ID_12365985,Human_RBP_ID_16998451,Human_RBP_ID_17687378,Human_RBP_ID_17857190,Human_RBP_ID_18545341,Human_RBP_ID_18652683,Human_RBP_ID_19909366,Human_RBP_ID_22711733,Human_RBP_ID_22798615,Human_RBP_ID_23126945,Human_RBP_ID_23628175,Human_RBP_ID_24471767,Human_RBP_ID_24558428,Human_RBP_ID_26748509,Human_RBP_ID_26756446,Human_RBP_ID_27646006 99947 RMVar_ID_99947 Human_SNP_ID_556790972 m1A Human chr14 - 58244938 58244938 58244938 ACTATTACACCGACAGACAGCGAACTCACCCCAGTGCCGATTGAGCTCATCGTGCTAAACCCAAA ACTATTACACCGACAGACAGCGAACTCACCCCGGTGCCGATTGAGCTCATCGTGCTAAACCCAAA T C ARMH4 Ensembl:ENSG00000139971 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:58244888..58244990 26863196 MeRIP-seq:(Medium) rs780981348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12366006 99948 RMVar_ID_99948 Human_SNP_ID_556794481 m1A Human chr14 - 58258000 58258000 58258000 ATCTGCCTTTTGAATAATTCACAAAATTTCTTACCTGCAGCCAAAAGGTCTAACAGCACTGTAGA ATCTGCCTTTTGAATAATTCACAAAATTTCTTGCCTGCAGCCAAAAGGTCTAACAGCACTGTAGA T C ARMH4 Ensembl:ENSG00000139971 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:58257950..58258050 32194978 MeRIP-seq:(Medium) rs1555352516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1237127,Human_RBP_ID_8077056 Clinvar_Rec_614 99949 RMVar_ID_99949 Human_SNP_ID_556797384 m1A Human chr14 - 58268302 58268302 58268302 CAGACAGGTGATTGACTAGACCTTGTTTATGTAGTTCTAATGTGGAATACTTAGAGTTGTTATGA CAGACAGGTGATTGACTAGACCTTGTTTATGTGGTTCTAATGTGGAATACTTAGAGTTGTTATGA T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs141776176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22495600 RMVar_hsa_circ_125022,RMVar_hsa_circ_166938 99950 RMVar_ID_99950 Human_SNP_ID_556822900 m1A Human chr14 + 58360864 58360864 58360864 TGGATAAGTAGAATGTTCATTTTTCGTAAAGCATTGGCCCTTCTCATACATTTTGTTGTTGTTGC TGGATAAGTAGAATGTTCATTTTTCGTAAAGCGTTGGCCCTTCTCATACATTTTGTTGTTGTTGC A G ARID4A Ensembl:ENSG00000032219 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:58360860..58360973 26863196 MeRIP-seq:(Medium) rs373975426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91708,RMVar_hsa_circ_166958 99951 RMVar_ID_99951 Human_SNP_ID_556839668 m1A Human chr14 - 58427113 58427113 58427113 TGTCCAGACCCTGACCCTCCCTCCCAAGGCTCAACCGTCCCCCAACAACCCCCAGCCTTGTACTG TGTCCAGACCCTGACCCTCCCTCCCAAGGCTCTACCGTCCCCCAACAACCCCCAGCCTTGTACTG T A TIMM9 Ensembl:ENSG00000100575 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:58423848..58427215 32194978 MeRIP-seq:(Medium) rs895352190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757987,Human_RBP_ID_5439145,Human_RBP_ID_17363336,Human_RBP_ID_18937327,Human_RBP_ID_26325133 Human_Splice_Rec_1519339,Human_Splice_Rec_1519349,Human_Splice_Rec_1519361,Human_Splice_Rec_1519369,Human_Splice_Rec_1519377,Human_Splice_Rec_1519385,Human_Splice_Rec_1519393,Human_Splice_Rec_1519399 RMVar_hsa_circ_37823 99952 RMVar_ID_99952 Human_SNP_ID_556839697 m1A Human chr14 + 58427163 58427163 58427163 GTCAGGGTCTGGACAGGAGCCGCGGCCGCCAGATGGGAAAGAACACGTGGGAGCAGTAATGTCAA GTCAGGGTCTGGACAGGAGCCGCGGCCGCCAGTTGGGAAAGAACACGTGGGAGCAGTAATGTCAA A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:58427034..58427186 26863410 MeRIP-seq:(Medium) rs1293921393 Functional Loss SNV dbSNP153 33..33 33 - - - 99953 RMVar_ID_99953 Human_SNP_ID_556891080 m1A Human chr14 + 58638332 58638332 58638332 AGAAGGGCGAGGCAGACACCGAGCGGCAGCGCACCCGGGAGCGGCAGGAGGCCACGCTGGCCGGG AGAAGGGCGAGGCAGACACCGAGCGGCAGCGCCCCCGGGAGCGGCAGGAGGCCACGCTGGCCGGG A C DACT1 Ensembl:ENSG00000165617 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:58637892..58638518 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 99954 RMVar_ID_99954 Human_SNP_ID_556891081 m1A Human chr14 + 58638332 58638332 58638332 AGAAGGGCGAGGCAGACACCGAGCGGCAGCGCACCCGGGAGCGGCAGGAGGCCACGCTGGCCGGG AGAAGGGCGAGGCAGACACCGAGCGGCAGCGCGCCCGGGAGCGGCAGGAGGCCACGCTGGCCGGG A G DACT1 Ensembl:ENSG00000165617 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:58637892..58638518 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 99955 RMVar_ID_99955 Human_SNP_ID_557056007 m1A Human chr14 + 59326990 59326990 59326990 CAGTGGAAAGAACAAGCGGAAAAAATGAGAAAAGGTAAATAATGAGGCCCTGATAAGAGGCTGTG CAGTGGAAAGAACAAGCGGAAAAAATGAGAAAGGGTAAATAATGAGGCCCTGATAAGAGGCTGTG A G DAAM1 Ensembl:ENSG00000100592 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59326973..59327038 26863196 MeRIP-seq:(Medium) rs1270189187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1520740,Human_Splice_Rec_1520741,Human_Splice_Rec_1520790,Human_Splice_Rec_1520791 RMVar_hsa_circ_268887,RMVar_hsa_circ_280592,RMVar_hsa_circ_166990,RMVar_hsa_circ_295103,RMVar_hsa_circ_67441,RMVar_hsa_circ_74896,RMVar_hsa_circ_166991,RMVar_hsa_circ_26745 99956 RMVar_ID_99956 Human_SNP_ID_557070583 m1A Human chr14 - 59384221 59384219 59384221 AAACAAAGACGCATGAAAGAAAGAAAGAAAGAAAGAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG AAACAAAGACGCATGAAAGAAAGAAAGAAAGA__GAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:59384080..59384255 26863196 MeRIP-seq:(Medium) rs71111631 Functional Loss DEL dbSNP153 33..34 33 - - - 99957 RMVar_ID_99957 Human_SNP_ID_557070584 m1A Human chr14 - 59384221 59384219 59384221 AAACAAAGACGCATGAAAGAAAGAAAGAAAGAAAGAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG AAACAAAGACGCATGAAAGAAAGAAAGAAAGA_AGAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG CTT CT - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:59384080..59384255 26863196 MeRIP-seq:(Medium) rs71111631 Functional Loss DEL dbSNP153 33..33 33 - - - 99958 RMVar_ID_99958 Human_SNP_ID_557070591 m1A Human chr14 - 59384221 59384221 59384221 AAACAAAGACGCATGAAAGAAAGAAAGAAAGAAAGAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG AAACAAAGACGCATGAAAGAAAGAAAGAAAGAGAGAAGAAAGAGAGAGAGAGGAAAGAAAGAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:59384080..59384255 26863196 MeRIP-seq:(Medium) rs1566521744 Functional Loss SNV dbSNP153 33..33 33 - - - 99959 RMVar_ID_99959 Human_SNP_ID_557074900 m1A Human chr14 - 59398992 59398992 59398992 TGGGGACAAGGTCAGAGGGCTGATGGTGCTGCACTGGTGTTCAGATCATTTAGGGTGGAGGAGGC TGGGGACAAGGTCAGAGGGCTGATGGTGCTGCTCTGGTGTTCAGATCATTTAGGGTGGAGGAGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59398943..59399272 26863196 MeRIP-seq:(Medium) rs1253143 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13151,GWAS_ID_13152,GWAS_ID_13153,GWAS_ID_13154,GWAS_ID_13155 99960 RMVar_ID_99960 Human_SNP_ID_557074901 m1A Human chr14 - 59398992 59398992 59398992 TGGGGACAAGGTCAGAGGGCTGATGGTGCTGCACTGGTGTTCAGATCATTTAGGGTGGAGGAGGC TGGGGACAAGGTCAGAGGGCTGATGGTGCTGCGCTGGTGTTCAGATCATTTAGGGTGGAGGAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59398943..59399272 26863196 MeRIP-seq:(Medium) rs1253143 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13151,GWAS_ID_13152,GWAS_ID_13153,GWAS_ID_13154,GWAS_ID_13155 99961 RMVar_ID_99961 Human_SNP_ID_557083236 m1A Human chr14 - 59426668 59426668 59426668 GAGCCCAGAGTATGGCAGCAGAGTAAAATGTGAGACAGCAAGACCAGTTAGTAGACGATGTTTTA GAGCCCAGAGTATGGCAGCAGAGTAAAATGTGGGACAGCAAGACCAGTTAGTAGACGATGTTTTA T C lnc-GPR135-1 RNACentral:URS00008B9F20 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:59426503..59426720 26863196 MeRIP-seq:(Medium) rs557854505 Functional Loss SNV dbSNP153 33..33 33 - - - 99962 RMVar_ID_99962 Human_SNP_ID_557083237 m1A Human chr14 - 59426673 59426673 59426673 AATTAGAGCCCAGAGTATGGCAGCAGAGTAAAATGTGAGACAGCAAGACCAGTTAGTAGACGATG AATTAGAGCCCAGAGTATGGCAGCAGAGTAAAGTGTGAGACAGCAAGACCAGTTAGTAGACGATG T C lnc-GPR135-1 RNACentral:URS00008B9F20 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59426443..59426759 26863196 MeRIP-seq:(Medium) rs1237205322 Functional Loss SNV dbSNP153 33..33 33 - - - 99963 RMVar_ID_99963 Human_SNP_ID_557083313 m1A Human chr14 + 59426973 59426973 59426973 TTCAGCCTTGCCATGTTCTTCATGGCCTCTGCATGTTTGTACATCCCCTTGCCTTTTCTGGGTTG TTCAGCCTTGCCATGTTCTTCATGGCCTCTGCGTGTTTGTACATCCCCTTGCCTTTTCTGGGTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:59426922..59427029 26863196 MeRIP-seq:(Medium) rs1254954884 Functional Loss SNV dbSNP153 33..33 33 - - - 99964 RMVar_ID_99964 Human_SNP_ID_557088587 m1A Human chr14 - 59447015 59447015 59447015 GGGTGATTAGGTTTTAATGAGATGGTAAGGGGAATGATCGGTCACCAAGGAGGGAGTAGAGGTAT GGGTGATTAGGTTTTAATGAGATGGTAAGGGGTATGATCGGTCACCAAGGAGGGAGTAGAGGTAT T A GPR135 Ensembl:ENSG00000181619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59446934..59447058 26863196 MeRIP-seq:(Medium) rs1243448510 Functional Loss SNV dbSNP153 33..33 33 - - - 99965 RMVar_ID_99965 Human_SNP_ID_557088588 m1A Human chr14 - 59447015 59447015 59447015 GGGTGATTAGGTTTTAATGAGATGGTAAGGGGAATGATCGGTCACCAAGGAGGGAGTAGAGGTAT GGGTGATTAGGTTTTAATGAGATGGTAAGGGGCATGATCGGTCACCAAGGAGGGAGTAGAGGTAT T G GPR135 Ensembl:ENSG00000181619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:59446934..59447058 26863196 MeRIP-seq:(Medium) rs1243448510 Functional Loss SNV dbSNP153 33..33 33 - - - 99966 RMVar_ID_99966 Human_SNP_ID_557088719 m1A Human chr14 - 59447427 59447427 59447427 GTTGTCTATGAAGCTTTGCGGCAGTACAGCCCAGGTAATTTGCTGAGCTTGATGGGTGTCAGGGT GTTGTCTATGAAGCTTTGCGGCAGTACAGCCCGGGTAATTTGCTGAGCTTGATGGGTGTCAGGGT T C GPR135 Ensembl:ENSG00000181619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:59447380..59447650 26863196 MeRIP-seq:(Medium) rs1050958354 Functional Loss SNV dbSNP153 33..33 33 - - - 99967 RMVar_ID_99967 Human_SNP_ID_557097828 m1A Human chr14 + 59484188 59484188 59484188 ATGTAGCGCCGCTTGGCCAGCAGGGTGGGCCCAGACACCTCCGGACACCCCGCCAGCACGATACG ATGTAGCGCCGCTTGGCCAGCAGGGTGGGCCCGGACACCTCCGGACACCCCGCCAGCACGATACG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:59484145..59484330 26863196 MeRIP-seq:(Medium) rs1338941786 Functional Loss SNV dbSNP153 33..33 33 - - - 99968 RMVar_ID_99968 Human_SNP_ID_557097871 m1A Human chr14 + 59484256 59484256 59484256 GGGCTCGCCGCCCGTGTGCATGTCCACCACCGACAGCACCGGCGTCCCTGGATCATGCGGGGGCA GGGCTCGCCGCCCGTGTGCATGTCCACCACCGGCAGCACCGGCGTCCCTGGATCATGCGGGGGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:59484206..59484359 26863196 MeRIP-seq:(Medium) rs1481491078 Functional Loss SNV dbSNP153 33..33 33 - - - 99969 RMVar_ID_99969 Human_SNP_ID_216022955 m1A Human chr4 + 180567235 180567232 180567236 GTGAGTGTGTGGGTGAGTGTGAGTGAGAAAGAATGAGTGAGGGTGTTTGTGGGTGAGTGTGAGTG GTGAGTGTGTGGGTGAGTGTGAGTGAGAAA____GAGTGAGGGTGTTTGTGGGTGAGTGTGAGTG AGAAT A HSALNG0038822 RNACentral:URS0000EB594F lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:180567184..180567297 26863196 MeRIP-seq:(Medium) rs1472738733 Functional Loss DEL dbSNP153 31..34 33 - - - 99970 RMVar_ID_99970 Human_SNP_ID_216442714 m1A Human chr4 - 182144107 182144107 182144107 TCGCGGGAGAGCCCAATCACGGGGCGAGCTGGACCTGGCTGTGATCATTTATAATCCTTGACTCC TCGCGGGAGAGCCCAATCACGGGGCGAGCTGGGCCTGGCTGTGATCATTTATAATCCTTGACTCC T C TENM3-AS1 Ensembl:ENSG00000177822 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:182144057..182144350 32194978 MeRIP-seq:(Medium) rs72693842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4778974,Human_RBP_ID_5426238 Human_Splice_Rec_624901,Human_Splice_Rec_624909,Human_Splice_Rec_624930,Human_Splice_Rec_624931,Human_Splice_Rec_624938,Human_Splice_Rec_624939,Human_Splice_Rec_624950,Human_Splice_Rec_624951 99971 RMVar_ID_99971 Human_SNP_ID_216442780 m1A Human chr4 + 182144220 182144213 182144220 CCTCGCACACTCCCGCACACACACACACACACACACACACGGACACGTGTACGCGCCCGGGCTCG CCTCGCACACTCCCGCACACACACAC_______CACACACGGACACGTGTACGCGCCCGGGCTCG CACACACA C TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:182144172..182144444 26863196 MeRIP-seq:(Medium) rs769500015 Functional Loss DEL dbSNP153 27..33 33 - - - 99972 RMVar_ID_99972 Human_SNP_ID_216442787 m1A Human chr4 + 182144220 182144220 182144220 CCTCGCACACTCCCGCACACACACACACACACACACACACGGACACGTGTACGCGCCCGGGCTCG CCTCGCACACTCCCGCACACACACACACACACGCACACACGGACACGTGTACGCGCCCGGGCTCG A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:182144172..182144444 26863196 MeRIP-seq:(Medium) rs867492818 Functional Loss SNV dbSNP153 33..33 33 - - - 99973 RMVar_ID_99973 Human_SNP_ID_216443008 m1A Human chr4 + 182144723 182144723 182144723 GGCTCGGGCGGACGCGGCGGCTGCTGCCGGGGAGCGAGCCGGCGGCGCGGGCGAGCCGAGCGCGG GGCTCGGGCGGACGCGGCGGCTGCTGCCGGGGGGCGAGCCGGCGGCGCGGGCGAGCCGAGCGCGG A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182144672..182145216 26863196 MeRIP-seq:(Medium) rs1042739322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249650,Human_RBP_ID_4778986 Human_Splice_Rec_624961 99974 RMVar_ID_99974 Human_SNP_ID_216443013 m1A Human chr4 + 182144727 182144727 182144727 CGGGCGGACGCGGCGGCTGCTGCCGGGGAGCGAGCCGGCGGCGCGGGCGAGCCGAGCGCGGTAAG CGGGCGGACGCGGCGGCTGCTGCCGGGGAGCGGGCCGGCGGCGCGGGCGAGCCGAGCGCGGTAAG A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:182144687..182144795;chr4:182144679..182144912 26863196 MeRIP-seq:(Medium) rs1222997389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249650 Human_Splice_Rec_624961 99975 RMVar_ID_99975 Human_SNP_ID_216467903 m1A Human chr4 + 182243446 182243443 182243446 CATGAAGGCTTTTAGATGGGTCTGGAGCTTGGAGGAGAAGTCTGAACTAAGGATAAACTAAAGGT CATGAAGGCTTTTAGATGGGTCTGGAGCTT___GGAGAAGTCTGAACTAAGGATAAACTAAAGGT TGGA T TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:182243444..182243686 26863196 MeRIP-seq:(Medium) rs1005292390 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_624965 99976 RMVar_ID_99976 Human_SNP_ID_216487397 m1A Human chr4 - 182323913 182323913 182323913 CTGTGAAGATACAAGGTTTGCATGAGGTCAGCATGACGTTCACCTAAAAACTGGCTACTCTCTAC CTGTGAAGATACAAGGTTTGCATGAGGTCAGCGTGACGTTCACCTAAAAACTGGCTACTCTCTAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:182323881..182323966 26863410 MeRIP-seq:(Medium) rs919537493 Functional Loss SNV dbSNP153 33..33 33 - - - 99977 RMVar_ID_99977 Human_SNP_ID_216487484 m1A Human chr4 + 182324125 182324125 182324125 AATTCCTCCGCAGACAATGAGGAGTGCCGGGTACCCACACAGAAGTCCTACAGTTCCAGCGAGAC AATTCCTCCGCAGACAATGAGGAGTGCCGGGTGCCCACACAGAAGTCCTACAGTTCCAGCGAGAC A G TENM3 Ensembl:ENSG00000218336 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:182324080..182324235 26863196 MeRIP-seq:(Medium) rs1273959635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96182,RMVar_hsa_circ_271370,RMVar_hsa_circ_282218,RMVar_hsa_circ_119113,RMVar_hsa_circ_229672,RMVar_hsa_circ_14204,RMVar_hsa_circ_47790,RMVar_hsa_circ_229673,RMVar_hsa_circ_229674,RMVar_hsa_circ_229671 99978 RMVar_ID_99978 Human_SNP_ID_216487516 m1A Human chr4 - 182324217 182324217 182324217 GTCTAGTGAACTCGTCTGCTTCTCTGTGAACCAAATCCTTCACTCTGTTGCCGTAAAGCAGCCGC GTCTAGTGAACTCGTCTGCTTCTCTGTGAACCGAATCCTTCACTCTGTTGCCGTAAAGCAGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:182323905..182324242 26863196 MeRIP-seq:(Medium) rs755542819 Functional Loss SNV dbSNP153 33..33 33 - - - 99979 RMVar_ID_99979 Human_SNP_ID_216518170 m1A Human chr4 + 182448838 182448838 182448838 GGGGGTGAGGCGAGGGGGTGAGGCGGCGGCCGAGCCGGGGCGCTGGGCGCGGGGCTGGCGGGAGG GGGGGTGAGGCGAGGGGGTGAGGCGGCGGCCGGGCCGGGGCGCTGGGCGCGGGGCTGGCGGGAGG A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182448784..182448989 26863196 MeRIP-seq:(Medium) rs1230474734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96182,RMVar_hsa_circ_119113,RMVar_hsa_circ_14204,RMVar_hsa_circ_47790,RMVar_hsa_circ_229673,RMVar_hsa_circ_229674,RMVar_hsa_circ_47100,RMVar_hsa_circ_341078,RMVar_hsa_circ_25767 99980 RMVar_ID_99980 Human_SNP_ID_216518299 m1A Human chr4 - 182449085 182449085 182449085 CCCCAGGCCGCCGCCGCCGCCGCCGCTCACCCACCTTGCCGCGGCGCGCCCTCGCTGTGGCCGTG CCCCAGGCCGCCGCCGCCGCCGCCGCTCACCCGCCTTGCCGCGGCGCGCCCTCGCTGTGGCCGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:182449044..182449242 26863196 MeRIP-seq:(Medium) rs1389020214 Functional Loss SNV dbSNP153 33..33 33 - - - 99981 RMVar_ID_99981 Human_SNP_ID_216518362 m1A Human chr4 - 182449194 182449188 182449194 CCGCCGCCGCCGCCGCCACCACCGCCACCGCCACCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC CCGCCGCCGCCGCCGCCACCACCGCCACCGCC______GCGGTCCCCGGAGCGAGCGAGCGACCC CGGCGGT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182449070..182449228 26863196 MeRIP-seq:(Medium) rs548937766 Functional Loss DEL dbSNP153 33..38 33 - - - 99982 RMVar_ID_99982 Human_SNP_ID_216518366 m1A Human chr4 - 182449194 182449194 182449194 CCGCCGCCGCCGCCGCCACCACCGCCACCGCCACCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC CCGCCGCCGCCGCCGCCACCACCGCCACCGCCTCCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182449070..182449228 26863196 MeRIP-seq:(Medium) rs1325639312 Functional Loss SNV dbSNP153 33..33 33 - - - 99983 RMVar_ID_99983 Human_SNP_ID_216518367 m1A Human chr4 - 182449194 182449194 182449194 CCGCCGCCGCCGCCGCCACCACCGCCACCGCCACCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC CCGCCGCCGCCGCCGCCACCACCGCCACCGCCGCCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182449070..182449228 26863196 MeRIP-seq:(Medium) rs1325639312 Functional Loss SNV dbSNP153 33..33 33 - - - 99984 RMVar_ID_99984 Human_SNP_ID_216518368 m1A Human chr4 - 182449194 182449194 182449194 CCGCCGCCGCCGCCGCCACCACCGCCACCGCCACCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC CCGCCGCCGCCGCCGCCACCACCGCCACCGCCCCCGCCGCGGTCCCCGGAGCGAGCGAGCGACCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182449070..182449228 26863196 MeRIP-seq:(Medium) rs1325639312 Functional Loss SNV dbSNP153 33..33 33 - - - 99985 RMVar_ID_99985 Human_SNP_ID_216518370 m1A Human chr4 - 182449200 182449200 182449200 GAGCCGCCGCCGCCGCCGCCGCCACCACCGCCACCGCCACCGCCGCGGTCCCCGGAGCGAGCGAG GAGCCGCCGCCGCCGCCGCCGCCACCACCGCCGCCGCCACCGCCGCGGTCCCCGGAGCGAGCGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:182449049..182449278 26863196 MeRIP-seq:(Medium) rs1431770785 Functional Loss SNV dbSNP153 33..33 33 - - - 99986 RMVar_ID_99986 Human_SNP_ID_216635216 m1A Human chr4 - 182905921 182905921 182905921 TAGATTGACTCCCCCCAAATGGTTCTGGTTGCAGTAGCTAGACAGGCATGCTGAGGAGGAGAAGC TAGATTGACTCCCCCCAAATGGTTCTGGTTGCGGTAGCTAGACAGGCATGCTGAGGAGGAGAAGC T C DCTD Ensembl:ENSG00000129187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:182905918..182906007 26863196 MeRIP-seq:(Medium) rs1380734511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229700,RMVar_hsa_circ_229699,RMVar_hsa_circ_377898,RMVar_hsa_circ_377439,RMVar_hsa_circ_229702,RMVar_hsa_circ_376790,RMVar_hsa_circ_298291,RMVar_hsa_circ_229705,RMVar_hsa_circ_348961 99987 RMVar_ID_99987 Human_SNP_ID_216635230 m1A Human chr4 + 182905977 182905977 182905977 GTCAATCTACCTCTTCCACCCTTTATCACGCCATCTTCCTGATGCTGCCCCTAAAATACACCCCA GTCAATCTACCTCTTCCACCCTTTATCACGCCTTCTTCCTGATGCTGCCCCTAAAATACACCCCA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182905973..182906083 26863196 MeRIP-seq:(Medium) rs572852023 Functional Loss SNV dbSNP153 33..33 33 - - - 99988 RMVar_ID_99988 Human_SNP_ID_216683512 m1A Human chr4 + 183099206 183099205 183099206 TGGGCGCCGCGACCCTCGGCGGCCAGAGGGGGACGGGGCGGAGGAGGAGGAAGAGGCGGAGGCAG TGGGCGCCGCGACCCTCGGCGGCCAGAGGGGG_CGGGGCGGAGGAGGAGGAAGAGGCGGAGGCAG GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr4:183099162..183099289;chr4:183099156..183099584 26863196 MeRIP-seq:(Medium) rs973220229 Functional Loss DEL dbSNP153 33..33 33 - - - 99989 RMVar_ID_99989 Human_SNP_ID_216683655 m1A Human chr4 + 183099574 183099574 183099574 GGAGGCCAGGGACTACGACGGCAAGGTCTTCTACATTGACCACAACACCAGGAGGACCAGCTGGA GGAGGCCAGGGACTACGACGGCAAGGTCTTCTGCATTGACCACAACACCAGGAGGACCAGCTGGA A G WWC2 Ensembl:ENSG00000151718 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:183099342..183099592 32194978 MeRIP-seq:(Medium) rs1023611022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941105,Human_RBP_ID_18195039,Human_RBP_ID_18821529,Human_RBP_ID_27824550 Human_Splice_Rec_625203,Human_Splice_Rec_625247,Human_Splice_Rec_625253,Human_Splice_Rec_625297 99990 RMVar_ID_99990 Human_SNP_ID_216724233 m1A Human chr4 + 183260932 183260932 183260932 TGTCTTTCAGCCTCTCTGCCAGCACCCTGTCCATGTCATCTGGGAGCAGCCTGGGTTCCCTGGCA TGTCTTTCAGCCTCTCTGCCAGCACCCTGTCCGTGTCATCTGGGAGCAGCCTGGGTTCCCTGGCA A G WWC2 Ensembl:ENSG00000151718 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:183253911..183260931 32194978 MeRIP-seq:(Medium) rs556011953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71756,Human_RBP_ID_941110,Human_RBP_ID_5211613,Human_RBP_ID_5531491,Human_RBP_ID_26350475 Human_Splice_Rec_625222,Human_Splice_Rec_625272,Human_Splice_Rec_625316,Human_Splice_Rec_625356,Human_Splice_Rec_625398,Human_Splice_Rec_625432 RMVar_hsa_circ_114561,RMVar_hsa_circ_351736,RMVar_hsa_circ_369144,RMVar_hsa_circ_364822,RMVar_hsa_circ_64397,RMVar_hsa_circ_67828,RMVar_hsa_circ_59806,RMVar_hsa_circ_75103,RMVar_hsa_circ_229710,RMVar_hsa_circ_127845,RMVar_hsa_circ_229714,RMVar_hsa_circ_44594,RMVar_hsa_circ_73243,RMVar_hsa_circ_353342,RMVar_hsa_circ_74472,RMVar_hsa_circ_351918,RMVar_hsa_circ_348335 99991 RMVar_ID_99991 Human_SNP_ID_216724335 m1A Human chr4 + 183261201 183261201 183261201 CAGCCTGGCCAGAGTGGACTCTGTGGAGTGGCAGCTGCAGCAACAGGCCACACTCCTCCACTGGC CAGCCTGGCCAGAGTGGACTCTGTGGAGTGGCGGCTGCAGCAACAGGCCACACTCCTCCACTGGC A G WWC2 Ensembl:ENSG00000151718 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:183261151..183261280 32194978 MeRIP-seq:(Medium) rs994222988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5531793,Human_RBP_ID_26350476 RMVar_hsa_circ_114561,RMVar_hsa_circ_351736,RMVar_hsa_circ_369144,RMVar_hsa_circ_364822,RMVar_hsa_circ_64397,RMVar_hsa_circ_67828,RMVar_hsa_circ_59806,RMVar_hsa_circ_75103,RMVar_hsa_circ_229710,RMVar_hsa_circ_127845,RMVar_hsa_circ_229714,RMVar_hsa_circ_44594,RMVar_hsa_circ_73243,RMVar_hsa_circ_353342,RMVar_hsa_circ_74472,RMVar_hsa_circ_351918,RMVar_hsa_circ_348335 99992 RMVar_ID_99992 Human_SNP_ID_216729602 m1A Human chr4 + 183280847 183280842 183280848 TTGTTAGCTGTGGAACAAGAATTAGCACAAGAAGAAGAAGAAGAATCAGGACAAGAAGAGCCAAG TTGTTAGCTGTGGAACAAGAATTAGCAC______AAGAAGAAGAATCAGGACAAGAAGAGCCAAG CAAGAAG C WWC2 Ensembl:ENSG00000151718 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:183280802..183280903 32194978 MeRIP-seq:(Medium) rs548940774 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_941112,Human_RBP_ID_1975418,Human_RBP_ID_7293500,Human_RBP_ID_9397524,Human_RBP_ID_15108851,Human_RBP_ID_22095749,Human_RBP_ID_24547813,Human_RBP_ID_26349666,Human_RBP_ID_27824553 Human_Splice_Rec_625234,Human_Splice_Rec_625235,Human_Splice_Rec_625284,Human_Splice_Rec_625285,Human_Splice_Rec_625328,Human_Splice_Rec_625368,Human_Splice_Rec_625369,Human_Splice_Rec_625414,Human_Splice_Rec_625415,Human_Splice_Rec_625444,Human_Splice_Rec_625445,Human_Splice_Rec_625462 RMVar_hsa_circ_351736,RMVar_hsa_circ_64397,RMVar_hsa_circ_67828,RMVar_hsa_circ_127845,RMVar_hsa_circ_229714,RMVar_hsa_circ_74472,RMVar_hsa_circ_269032,RMVar_hsa_circ_347203,RMVar_hsa_circ_356988,RMVar_hsa_circ_344257,RMVar_hsa_circ_111101,RMVar_hsa_circ_229716,RMVar_hsa_circ_229717,RMVar_hsa_circ_229715 99993 RMVar_ID_99993 Human_SNP_ID_216729603 m1A Human chr4 + 183280847 183280842 183280848 TTGTTAGCTGTGGAACAAGAATTAGCACAAGAAGAAGAAGAAGAATCAGGACAAGAAGAGCCAAG TTGTTAGCTGTGGAACAAGAATTAGCACAAG___AAGAAGAAGAATCAGGACAAGAAGAGCCAAG CAAGAAG CAAG WWC2 Ensembl:ENSG00000151718 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:183280802..183280903 32194978 MeRIP-seq:(Medium) rs548940774 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_941112,Human_RBP_ID_1975418,Human_RBP_ID_7293500,Human_RBP_ID_9397524,Human_RBP_ID_15108851,Human_RBP_ID_22095749,Human_RBP_ID_24547813,Human_RBP_ID_26349666,Human_RBP_ID_27824553 Human_Splice_Rec_625234,Human_Splice_Rec_625235,Human_Splice_Rec_625284,Human_Splice_Rec_625285,Human_Splice_Rec_625328,Human_Splice_Rec_625368,Human_Splice_Rec_625369,Human_Splice_Rec_625414,Human_Splice_Rec_625415,Human_Splice_Rec_625444,Human_Splice_Rec_625445,Human_Splice_Rec_625462 RMVar_hsa_circ_351736,RMVar_hsa_circ_64397,RMVar_hsa_circ_67828,RMVar_hsa_circ_127845,RMVar_hsa_circ_229714,RMVar_hsa_circ_74472,RMVar_hsa_circ_269032,RMVar_hsa_circ_347203,RMVar_hsa_circ_356988,RMVar_hsa_circ_344257,RMVar_hsa_circ_111101,RMVar_hsa_circ_229716,RMVar_hsa_circ_229717,RMVar_hsa_circ_229715 99994 RMVar_ID_99994 Human_SNP_ID_216730559 m1A Human chr4 - 183284435 183284434 183284435 GTCCTTTGCAGGCCACTCCCTACCAGCAGGGAAGAAGCTGCAGTCCCAGCGCCTCACCACGAGCA GTCCTTTGCAGGCCACTCCCTACCAGCAGGGA_GAAGCTGCAGTCCCAGCGCCTCACCACGAGCA CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:183284388..183289397 32194978 MeRIP-seq:(Medium) rs748985946 Functional Loss DEL dbSNP153 33..33 33 - - - 99995 RMVar_ID_99995 Human_SNP_ID_216762739 m1A Human chr4 - 183407909 183407908 183407910 AAAGAAGGAAGAAGAGAAAGAAGAAAAGAAAGAAAAAAAGGAGAGGAAGAAAGAAGAAAGAGAAA AAAGAAGGAAGAAGAGAAAGAAGAAAAGAAA__AAAAAAGGAGAGGAAGAAAGAAGAAAGAGAAA TTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183407662..183408104 26863196 MeRIP-seq:(Medium) rs1261141836 Functional Loss DEL dbSNP153 32..33 33 - - - 99996 RMVar_ID_99996 Human_SNP_ID_216773129 m1A Human chr4 - 183444700 183444700 183444700 CCTGTCACTGCGGCCTGCACCCGCGGCCCTCCAGATAACGCCCCTCCGCAGGCCTAAAGACCAAA CCTGTCACTGCGGCCTGCACCCGCGGCCCTCCGGATAACGCCCCTCCGCAGGCCTAAAGACCAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:183444651..183444900;chr4:183444651..183444875 26863196 MeRIP-seq:(Medium) rs760678752 Functional Loss SNV dbSNP153 33..33 33 - - - 99997 RMVar_ID_99997 Human_SNP_ID_216773146 m1A Human chr4 + 183444730 183444730 183444730 TCTGGAGGGCCGCGGGTGCAGGCCGCAGTGACAGGGCCGCTCGCCCCGCTAGTCCTGCCTGTCTC TCTGGAGGGCCGCGGGTGCAGGCCGCAGTGACGGGGCCGCTCGCCCCGCTAGTCCTGCCTGTCTC A G CDKN2AIP Ensembl:ENSG00000168564 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr4:183444685..183444841;chr4:183444683..183444831 26863196 MeRIP-seq:(Medium) rs1414439901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4779477,Human_RBP_ID_18424828 99998 RMVar_ID_99998 Human_SNP_ID_216773159 m1A Human chr4 + 183444748 183444748 183444748 CAGGCCGCAGTGACAGGGCCGCTCGCCCCGCTAGTCCTGCCTGTCTCCCGGTGCAGCTGTGTTCG CAGGCCGCAGTGACAGGGCCGCTCGCCCCGCTCGTCCTGCCTGTCTCCCGGTGCAGCTGTGTTCG A C CDKN2AIP Ensembl:ENSG00000168564 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:183444698..183444875 26863196 MeRIP-seq:(Medium) rs768453921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4779479,Human_RBP_ID_18424828 99999 RMVar_ID_99999 Human_SNP_ID_216773160 m1A Human chr4 + 183444748 183444748 183444748 CAGGCCGCAGTGACAGGGCCGCTCGCCCCGCTAGTCCTGCCTGTCTCCCGGTGCAGCTGTGTTCG CAGGCCGCAGTGACAGGGCCGCTCGCCCCGCTGGTCCTGCCTGTCTCCCGGTGCAGCTGTGTTCG A G CDKN2AIP Ensembl:ENSG00000168564 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:183444698..183444875 26863196 MeRIP-seq:(Medium) rs768453921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4779479,Human_RBP_ID_18424828 100000 RMVar_ID_100000 Human_SNP_ID_216773162 m1A Human chr4 - 183444750 183444750 183444750 CGCGAACACAGCTGCACCGGGAGACAGGCAGGACTAGCGGGGCGAGCGGCCCTGTCACTGCGGCC CGCGAACACAGCTGCACCGGGAGACAGGCAGGGCTAGCGGGGCGAGCGGCCCTGTCACTGCGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183444704..183444826 26863196 MeRIP-seq:(Medium) rs1168709725 Functional Loss SNV dbSNP153 33..33 33 - - - 100001 RMVar_ID_100001 Human_SNP_ID_216788588 m1A Human chr4 + 183504790 183504790 183504790 GGGGCAGGCTAGCGGGAGGCTCTCCGTGAGGCACGGAGGGTGACTGGGGACAGGCGGGCGGCGAC GGGGCAGGCTAGCGGGAGGCTCTCCGTGAGGCCCGGAGGGTGACTGGGGACAGGCGGGCGGCGAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183504713..183505157 26863196 MeRIP-seq:(Medium) rs940132809 Functional Loss SNV dbSNP153 33..33 33 - - - 100002 RMVar_ID_100002 Human_SNP_ID_216788594 m1A Human chr4 + 183504800 183504800 183504800 AGCGGGAGGCTCTCCGTGAGGCACGGAGGGTGACTGGGGACAGGCGGGCGGCGACGGGCTTGTCA AGCGGGAGGCTCTCCGTGAGGCACGGAGGGTGGCTGGGGACAGGCGGGCGGCGACGGGCTTGTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183504749..183504993 26863196 MeRIP-seq:(Medium) rs996836728 Functional Loss SNV dbSNP153 33..33 33 - - - 100003 RMVar_ID_100003 Human_SNP_ID_216789206 m1A Human chr4 + 183506164 183506164 183506164 CGAGAGGGGCGGTGGCGAGCTGGCTGCTGGGGAGGGAGTCGGGGCTGTGCGGGGGCGTTGGTTCG CGAGAGGGGCGGTGGCGAGCTGGCTGCTGGGGGGGGAGTCGGGGCTGTGCGGGGGCGTTGGTTCG A G ING2 Ensembl:ENSG00000168556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183506148..183506239 26863196 MeRIP-seq:(Medium) rs866863018 Functional Loss SNV dbSNP153 33..33 33 - - - 100004 RMVar_ID_100004 Human_SNP_ID_216791464 m1A Human chr4 - 183514753 183514753 183514753 TCACTTGCCCCTCCTAACGGGATTCCTCCAGCATATAGTCAATCATGCCATACTATTTCCCGAAT TCACTTGCCCCTCCTAACGGGATTCCTCCAGCGTATAGTCAATCATGCCATACTATTTCCCGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183514708..183514808 26863196 MeRIP-seq:(Medium) rs1485127666 Functional Loss SNV dbSNP153 33..33 33 - - - 100005 RMVar_ID_100005 Human_SNP_ID_216867016 m1A Human chr4 - 183797376 183797368 183797376 CGGCCTCGGCACCCTCGCCTCCCCGGGCGCCCAGCGGCCCCGCGGGGGCGGAGACGCGGGAGGAG CGGCCTCGGCACCCTCGCCTCCCCGGGCGCCC________CGCGGGGGCGGAGACGCGGGAGGAG GGGGCCGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183797326..183797391 26863196 MeRIP-seq:(Medium) rs1158331895 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_27507406 100006 RMVar_ID_100006 Human_SNP_ID_216867331 m1A Human chr4 + 183798391 183798391 183798391 CGGCTCGGAGGGCGCGGCGCTCGGGGCGCGTGAGTGTCCCCCTCCCGGCACTGCTCCGCGGCTGG CGGCTCGGAGGGCGCGGCGCTCGGGGCGCGTGGGTGTCCCCCTCCCGGCACTGCTCCGCGGCTGG A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183798341..183798559 26863196 MeRIP-seq:(Medium) rs1321859463 Functional Loss SNV dbSNP153 33..33 33 - - - 100007 RMVar_ID_100007 Human_SNP_ID_216867336 m1A Human chr4 - 183798410 183798410 183798410 TCCGCCCGGCCCGCGCACTCCAGCCGCGGAGCAGTGCCGGGAGGGGGACACTCACGCGCCCCGAG TCCGCCCGGCCCGCGCACTCCAGCCGCGGAGCGGTGCCGGGAGGGGGACACTCACGCGCCCCGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183798360..183798537 26863196 MeRIP-seq:(Medium) rs1015474471 Functional Loss SNV dbSNP153 33..33 33 - - - 100008 RMVar_ID_100008 Human_SNP_ID_216868102 m1A Human chr4 + 183801825 183801825 183801825 GAAGCCACTGGAGGCTTCTAAGCAAGGGTGGGAATGAAGTGATTTGATCTGTGTTACAATGAGAA GAAGCCACTGGAGGCTTCTAAGCAAGGGTGGGCATGAAGTGATTTGATCTGTGTTACAATGAGAA A C STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183801711..183801857 26863196 MeRIP-seq:(Medium) rs1259126925 Functional Loss SNV dbSNP153 33..33 33 - - - 100009 RMVar_ID_100009 Human_SNP_ID_216872453 m1A Human chr4 + 183819425 183819425 183819425 AAACCAGTCAGGCATGGCGGCGCGCGCCCACAATCGCAGGCACTGGGCAGGTTGAGGCAGGAGAA AAACCAGTCAGGCATGGCGGCGCGCGCCCACAGTCGCAGGCACTGGGCAGGTTGAGGCAGGAGAA A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183819407..183819516 26863196 MeRIP-seq:(Medium) rs1187867912 Functional Loss SNV dbSNP153 33..33 33 - - - 100010 RMVar_ID_100010 Human_SNP_ID_216880223 m1A Human chr4 + 183851045 183851045 183851045 AGGATGAGAGAAACGATGAGGGAAAGGATGAGAGAAACGATGAGAGAAAGGATGAGGGAAAGGAT AGGATGAGAGAAACGATGAGGGAAAGGATGAGGGAAACGATGAGAGAAAGGATGAGGGAAAGGAT A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:183850891..183851301 26863196 MeRIP-seq:(Medium) rs376506542 Functional Loss SNV dbSNP153 33..33 33 - - - 100011 RMVar_ID_100011 Human_SNP_ID_216880224 m1A Human chr4 - 183851053 183851050 183851053 TTTCTCTCATCCTTTCCCTCATCCTTTCTCTCATCGTTTCTCTCATCCTTTCCCTCATCGTTTCT TTTCTCTCATCCTTTCCCTCATCCTTTCTCTC___GTTTCTCTCATCCTTTCCCTCATCGTTTCT CGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183850760..183851527 26863196 MeRIP-seq:(Medium) rs1299558619 Functional Loss DEL dbSNP153 33..35 33 - - - 100012 RMVar_ID_100012 Human_SNP_ID_216880401 m1A Human chr4 + 183851400 183851399 183851400 AGGATGAGAGAAACGATGAGGGAAAGGATGAGAGGATGAGAGAAAGGATGAGGGAAAGGATGAGA AGGATGAGAGAAACGATGAGGGAAAGGATGAG_GGATGAGAGAAAGGATGAGGGAAAGGATGAGA GA G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183851353..183851508 26863196 MeRIP-seq:(Medium) rs1336489934 Functional Loss DEL dbSNP153 33..33 33 - - - 100013 RMVar_ID_100013 Human_SNP_ID_216880430 m1A Human chr4 - 183851464 183851461 183851464 TTTCCCTCATCCTTTCCCTCATCGTTTCTCTCATCGTTTCTCTCATCCTTTCCCTCATCCTTTCT TTTCCCTCATCCTTTCCCTCATCGTTTCTCTC___GTTTCTCTCATCCTTTCCCTCATCCTTTCT CGAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:183851374..183851503 26863196 MeRIP-seq:(Medium) rs1379136470 Functional Loss DEL dbSNP153 33..35 33 - - - 100014 RMVar_ID_100014 Human_SNP_ID_216880537 m1A Human chr4 + 183851768 183851768 183851768 AGGATGAGGGAAAGGATGAGAGAAAGGATGAGAGAAAGGATGAGGGAAAGGATGAGAGAAAGGAT AGGATGAGGGAAAGGATGAGAGAAAGGATGAGGGAAAGGATGAGGGAAAGGATGAGAGAAAGGAT A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183851712..183851913 26863196 MeRIP-seq:(Medium) rs200599549 Functional Loss SNV dbSNP153 33..33 33 - - - 100015 RMVar_ID_100015 Human_SNP_ID_216880538 m1A Human chr4 + 183851770 183851769 183851771 GATGAGGGAAAGGATGAGAGAAAGGATGAGAGAAAGGATGAGGGAAAGGATGAGAGAAAGGATGA GATGAGGGAAAGGATGAGAGAAAGGATGAGAG__AGGATGAGGGAAAGGATGAGAGAAAGGATGA GAA G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183851730..183851821 26863196 MeRIP-seq:(Medium) rs1338148416 Functional Loss DEL dbSNP153 33..34 33 - - - 100016 RMVar_ID_100016 Human_SNP_ID_216880696 m1A Human chr4 + 183852363 183852361 183852364 GGGAAAGGATGAGGGAAAGGATGAGAGAAACGATGAGGGAAAGGATGAGAGAAAGGATGAGAGAA GGGAAAGGATGAGGGAAAGGATGAGAGAAAC___GAGGGAAAGGATGAGAGAAAGGATGAGAGAA CGAT C STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:183852334..183852406 26863196 MeRIP-seq:(Medium) rs1297211176 Functional Loss DEL dbSNP153 32..34 33 - - - 100017 RMVar_ID_100017 Human_SNP_ID_216880789 m1A Human chr4 + 183852592 183852592 183852592 AGAAAGGATGAGGGAAAGGATGATGCTGCCTTATCATACTCTCATCAAGGTTAATTCTAGGTTGA AGAAAGGATGAGGGAAAGGATGATGCTGCCTTGTCATACTCTCATCAAGGTTAATTCTAGGTTGA A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183852542..183852626 26863196 MeRIP-seq:(Medium) rs549733855 Functional Loss SNV dbSNP153 33..33 33 - - - 100018 RMVar_ID_100018 Human_SNP_ID_216884151 m1A Human chr4 + 183865774 183865774 183865774 AACGAAATGGCATGAACACAGGCTAGAAGGCAAGAAAACCCTGGTTGTAGGTTGCATGGAGAAGT AACGAAATGGCATGAACACAGGCTAGAAGGCACGAAAACCCTGGTTGTAGGTTGCATGGAGAAGT A C STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:183865644..183865821 26863196 MeRIP-seq:(Medium) rs1318595036 Functional Loss SNV dbSNP153 33..33 33 - - - 100019 RMVar_ID_100019 Human_SNP_ID_216909147 m1A Human chr4 + 183967488 183967488 183967488 TGAGTGGTGCAAGAGGAAGAAAGGGGAACATGATGGTGTTTGGTGTCTTTAAGGAAGAGTGAAGG TGAGTGGTGCAAGAGGAAGAAAGGGGAACATGTTGGTGTTTGGTGTCTTTAAGGAAGAGTGAAGG A T STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183967440..183967579 26863196 MeRIP-seq:(Medium) rs1019245161 Functional Loss SNV dbSNP153 33..33 33 - - - 100020 RMVar_ID_100020 Human_SNP_ID_216919652 m1A Human chr4 + 184010872 184010872 184010872 TCGGGAGGAGTGGCTGAAGGGATCGCCAACGGACGCCTCGTCCAGCACCATGGTGCCGAGCCCAG TCGGGAGGAGTGGCTGAAGGGATCGCCAACGGGCGCCTCGTCCAGCACCATGGTGCCGAGCCCAG A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:184010822..184010922 26863196 MeRIP-seq:(Medium) rs1187988949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229755,RMVar_hsa_circ_229754,RMVar_hsa_circ_294964,RMVar_hsa_circ_277715 100021 RMVar_ID_100021 Human_SNP_ID_217015269 m1A Human chr4 - 184389048 184389048 184389048 TACTTTCTTGAAAGGGGCGGCCACACTGGCGGAAGAGGAATATTGAAGGCAAACAGTACCTCAGC TACTTTCTTGAAAGGGGCGGCCACACTGGCGGGAGAGGAATATTGAAGGCAAACAGTACCTCAGC T C IRF2 Ensembl:ENSG00000168310 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:184389001..184389075 32194978 MeRIP-seq:(Medium) rs773093316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_626028,Human_Splice_Rec_626040,Human_Splice_Rec_626046 100022 RMVar_ID_100022 Human_SNP_ID_217025423 m1A Human chr4 + 184430487 184430487 184430487 ACCTAGCCTCCTCCTCCACAAGGGCTTCCCAGACCACTCCCGCCTAAAGTAGTCCCTCTGCCTCC ACCTAGCCTCCTCCTCCACAAGGGCTTCCCAGGCCACTCCCGCCTAAAGTAGTCCCTCTGCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:184430406..184430508 26863196 MeRIP-seq:(Medium) rs761404590 Functional Loss SNV dbSNP153 33..33 33 - - - 100023 RMVar_ID_100023 Human_SNP_ID_217036090 m1A Human chr4 + 184474871 184474870 184474871 AGCAGCGGCTCGTGAGTCCGCGGCTCGCACCCAGGGGCGCCCGCACGTGCGGCTAGAACGTCCGA AGCAGCGGCTCGTGAGTCCGCGGCTCGCACCC_GGGGCGCCCGCACGTGCGGCTAGAACGTCCGA CA C AC099343.4 Ensembl:ENSG00000271646 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:184474828..184475085 26863196 MeRIP-seq:(Medium) rs1375330014 Functional Loss DEL dbSNP153 33..33 33 - - - 100024 RMVar_ID_100024 Human_SNP_ID_217078100 m1A Human chr4 - 184648862 184648862 184648862 AGGCAGCGGCAAGCTGGGAAACGGACGGCGCTACCGCCGGCGGAGGAGTGGCCCCGGGAAGCGGT AGGCAGCGGCAAGCTGGGAAACGGACGGCGCTGCCGCCGGCGGAGGAGTGGCCCCGGGAAGCGGT T C CASP3 Ensembl:ENSG00000164305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:184648851..184649014 26863196 MeRIP-seq:(Medium) rs1027532184 Functional Loss SNV dbSNP153 33..33 33 - - - 100025 RMVar_ID_100025 Human_SNP_ID_217079503 m1A Human chr4 + 184653104 184653101 184653105 AGGAAAGAAGGGAAGGAAGGAGGGAAAGAAGAAGGAAGGAAGGAAGGTAGGTAGGTGAGAAAGAA AGGAAAGAAGGGAAGGAAGGAGGGAAAGAA____GAAGGAAGGAAGGTAGGTAGGTGAGAAAGAA AGAAG A PRIMPOL Ensembl:ENSG00000164306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:184653100..184653319 26863196 MeRIP-seq:(Medium) rs1483227291 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_70563,RMVar_hsa_circ_356228,RMVar_hsa_circ_268212,RMVar_hsa_circ_336998,RMVar_hsa_circ_353567,RMVar_hsa_circ_320016,RMVar_hsa_circ_229773,RMVar_hsa_circ_229774 100026 RMVar_ID_100026 Human_SNP_ID_217079504 m1A Human chr4 + 184653104 184653102 184653104 AGGAAAGAAGGGAAGGAAGGAGGGAAAGAAGAAGGAAGGAAGGAAGGTAGGTAGGTGAGAAAGAA AGGAAAGAAGGGAAGGAAGGAGGGAAAGAAG__GGAAGGAAGGAAGGTAGGTAGGTGAGAAAGAA GAA G PRIMPOL Ensembl:ENSG00000164306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:184653100..184653319 26863196 MeRIP-seq:(Medium) rs139160884 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_70563,RMVar_hsa_circ_356228,RMVar_hsa_circ_268212,RMVar_hsa_circ_336998,RMVar_hsa_circ_353567,RMVar_hsa_circ_320016,RMVar_hsa_circ_229773,RMVar_hsa_circ_229774 100027 RMVar_ID_100027 Human_SNP_ID_217092678 m1A Human chr4 - 184700845 184700845 184700845 TTTCAGATATCGAAAAGAAAAGGCAGCGTATGATTGAAGTCCAGGATGAACTGCTTCGGTAAGAT TTTCAGATATCGAAAAGAAAAGGCAGCGTATGCTTGAAGTCCAGGATGAACTGCTTCGGTAAGAT T G CENPU Ensembl:ENSG00000151725 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:184700838..184702144 32194978 MeRIP-seq:(Medium) rs370121029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617993,Human_RBP_ID_7294340,Human_RBP_ID_9349534,Human_RBP_ID_15110794,Human_RBP_ID_22510524,Human_RBP_ID_24048251,Human_RBP_ID_25829669 Human_Splice_Rec_626368,Human_Splice_Rec_626369,Human_Splice_Rec_626398,Human_Splice_Rec_626399 RMVar_hsa_circ_27801,RMVar_hsa_circ_17811 100028 RMVar_ID_100028 Human_SNP_ID_217096507 m1A Human chr4 - 184716465 184716465 184716465 TTTCAGAGAAACCAGCTGAGTCTGTCACTTCTAAAAAGACAGGACCCCTTAGTGCCCAGCCCTCT TTTCAGAGAAACCAGCTGAGTCTGTCACTTCTGAAAAGACAGGACCCCTTAGTGCCCAGCCCTCT T C CENPU Ensembl:ENSG00000151725 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:184716414..184716513 32194978 MeRIP-seq:(Medium) rs1400647518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9154128,Human_RBP_ID_9397532,Human_RBP_ID_27825208 Human_Splice_Rec_626359,Human_Splice_Rec_626383 RMVar_hsa_circ_13631,RMVar_hsa_circ_229795,RMVar_hsa_circ_17811,RMVar_hsa_circ_283488,RMVar_hsa_circ_348189,RMVar_hsa_circ_53618,RMVar_hsa_circ_269857,RMVar_hsa_circ_229794,RMVar_hsa_circ_362585,RMVar_hsa_circ_50961 100029 RMVar_ID_100029 Human_SNP_ID_217101230 m1A Human chr4 - 184734065 184734065 184734065 GAGCTTCCAGTCGCTCGAGAGCGGAGAGCGGCACCATGGCCCCGCGGGGGCGGCGGCGGCCGCGG GAGCTTCCAGTCGCTCGAGAGCGGAGAGCGGCCCCATGGCCCCGCGGGGGCGGCGGCGGCCGCGG T G CENPU Ensembl:ENSG00000151725 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:184733966..184734070;chr4:184733951..184734096 26863196 MeRIP-seq:(Medium) rs772868874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4795203,Human_RBP_ID_18424655 Human_Splice_Rec_626349,Human_Splice_Rec_626373 100030 RMVar_ID_100030 Human_SNP_ID_217207035 m1A Human chr4 - 185143345 185143345 185143345 CCCATGGTGACAGCTCGACGCTCTCAGCCCGCAGGCAGCCCGTTCGTGCTCTCGCCCACGCCCGG CCCATGGTGACAGCTCGACGCTCTCAGCCCGCCGGCAGCCCGTTCGTGCTCTCGCCCACGCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:185143294..185143413 26863196 MeRIP-seq:(Medium) rs1360034095 Functional Loss SNV dbSNP153 33..33 33 - - - 100031 RMVar_ID_100031 Human_SNP_ID_217207577 m1A Human chr4 + 185145139 185145139 185145139 GTGAGTTCCATGGTCTGGGCGACTGTATCATCAAGATCTTCAAGTCTGATGGCCTGAGGGGGCTC GTGAGTTCCATGGTCTGGGCGACTGTATCATCTAGATCTTCAAGTCTGATGGCCTGAGGGGGCTC A T SLC25A4 Ensembl:ENSG00000151729 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:185143290..185145374 32194978 MeRIP-seq:(Medium) rs780055096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1975527,Human_RBP_ID_4779919,Human_RBP_ID_22458525 RMVar_hsa_circ_265306 100032 RMVar_ID_100032 Human_SNP_ID_217222878 m1A Human chr4 - 185203883 185203883 185203883 GGTGGCCGCGGCTCTCAGGTGAGGGGCGCGCGAGCGGCTCCTGGCTCCCTGCTCGCGGGGCGCCC GGTGGCCGCGGCTCTCAGGTGAGGGGCGCGCGGGCGGCTCCTGGCTCCCTGCTCGCGGGGCGCCC T C CFAP97 Ensembl:ENSG00000164323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:185203835..185203947;chr4:185203832..185203933 26863196 MeRIP-seq:(Medium) rs951502876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794772 Human_Splice_Rec_627557 100033 RMVar_ID_100033 Human_SNP_ID_217222946 m1A Human chr4 - 185204041 185204041 185204041 ACGAGGCCCGGCGTGCGCCCCCGCCTCTCCCGAAGCGCCGGGCCCCACGCCGCCCCTCCTTTCCC ACGAGGCCCGGCGTGCGCCCCCGCCTCTCCCGGAGCGCCGGGCCCCACGCCGCCCCTCCTTTCCC T C CFAP97 Ensembl:ENSG00000164323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185204013..185204115 26863196 MeRIP-seq:(Medium) rs1467289331 Functional Loss SNV dbSNP153 33..33 33 - - - 100034 RMVar_ID_100034 Human_SNP_ID_217235236 m1A Human chr4 + 185247241 185247241 185247241 ATGGCATTTCATACCTTTGATTTTTTTTTTTTATGTGATTTATTCATTCAGTAATCTGCTTTGTA ATGGCATTTCATACCTTTGATTTTTTTTTTTTGTGTGATTTATTCATTCAGTAATCTGCTTTGTA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:185247237..185247324 26863196 MeRIP-seq:(Medium) rs1455445568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 100035 RMVar_ID_100035 Human_SNP_ID_217235237 m1A Human chr4 + 185247241 185247241 185247241 ATGGCATTTCATACCTTTGATTTTTTTTTTTTATGTGATTTATTCATTCAGTAATCTGCTTTGTA ATGGCATTTCATACCTTTGATTTTTTTTTTTTTTGTGATTTATTCATTCAGTAATCTGCTTTGTA A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:185247237..185247324 26863196 MeRIP-seq:(Medium) rs1455445568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 100036 RMVar_ID_100036 Human_SNP_ID_217254671 m1A Human chr4 + 185329674 185329674 185329674 AGGGCCTCTTGGATTGGAGCCGCATGAGGAAGACAGACACAGAGAGAGAGAGAGAGAGAGAAGAG AGGGCCTCTTGGATTGGAGCCGCATGAGGAAGGCAGACACAGAGAGAGAGAGAGAGAGAGAAGAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185329627..185329748 26863196 MeRIP-seq:(Medium) rs947417866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117822,RMVar_hsa_circ_346452,RMVar_hsa_circ_340568,RMVar_hsa_circ_92358,RMVar_hsa_circ_109238,RMVar_hsa_circ_75720,RMVar_hsa_circ_117752,RMVar_hsa_circ_229815,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229825,RMVar_hsa_circ_229833,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046,RMVar_hsa_circ_229837,RMVar_hsa_circ_272192,RMVar_hsa_circ_229836,RMVar_hsa_circ_326975,RMVar_hsa_circ_229838,RMVar_hsa_circ_293171,RMVar_hsa_circ_301734,RMVar_hsa_circ_314792,RMVar_hsa_circ_40701 100037 RMVar_ID_100037 Human_SNP_ID_217320169 m1A Human chr4 + 185587577 185587577 185587577 CGGGAGGCCCGCGGGGTGTTTCAGGCGCGTTGACGCAGGTGCATGGCTGGCAGGCGGCCTCTACA CGGGAGGCCCGCGGGGTGTTTCAGGCGCGTTGGCGCAGGTGCATGGCTGGCAGGCGGCCTCTACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:185587526..185587601 26863196 MeRIP-seq:(Medium) rs375252999 Functional Loss SNV dbSNP153 33..33 33 - - - 100038 RMVar_ID_100038 Human_SNP_ID_217324971 m1A Human chr4 - 185606667 185606666 185606667 CATTGAAGAGGAGGAGGAGGAGGAGAAACCCAACTGCCTAAAACACCCCATAGCCACCCCCACAG CATTGAAGAGGAGGAGGAGGAGGAGAAACCCATGTGCCTAAAACACCCCATAGCCACCCCCACAG GT CA SORBS2 Ensembl:ENSG00000154556 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185606660..185606748 26863196 MeRIP-seq:(Medium) rs34661953 Functional Loss MNV dbSNP153 33..34 33 - - - Human_Splice_Rec_628241 RMVar_hsa_circ_22939,RMVar_hsa_circ_72447,RMVar_hsa_circ_358706,RMVar_hsa_circ_63830,RMVar_hsa_circ_71563,RMVar_hsa_circ_73995 100039 RMVar_ID_100039 Human_SNP_ID_217324972 m1A Human chr4 - 185606667 185606667 185606667 CATTGAAGAGGAGGAGGAGGAGGAGAAACCCAACTGCCTAAAACACCCCATAGCCACCCCCACAG CATTGAAGAGGAGGAGGAGGAGGAGAAACCCAGCTGCCTAAAACACCCCATAGCCACCCCCACAG T C SORBS2 Ensembl:ENSG00000154556 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185606660..185606748 26863196 MeRIP-seq:(Medium) rs1381095492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_628241 RMVar_hsa_circ_22939,RMVar_hsa_circ_72447,RMVar_hsa_circ_358706,RMVar_hsa_circ_63830,RMVar_hsa_circ_71563,RMVar_hsa_circ_73995 100040 RMVar_ID_100040 Human_SNP_ID_217356360 m1A Human chr4 - 185731537 185731512 185731538 AGATAGGCAGGGAGGGAGGGAGAGAGGCAGGGAGAGAGGGAGGGGGAGAGAGATAGGCAGGGAGG AGATAGGCAGGGAGGGAGGGAGAGAGGCAGG__________________________CAGGGAGG GCCTATCTCTCTCCCCCTCCCTCTCTC G SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:185731533..185731730 26863196 MeRIP-seq:(Medium) rs1294681852 Functional Loss DEL dbSNP153 32..57 33 - - - RMVar_hsa_circ_324587,RMVar_hsa_circ_365326,RMVar_hsa_circ_358337,RMVar_hsa_circ_41303 100041 RMVar_ID_100041 Human_SNP_ID_217358869 m1A Human chr4 + 185740696 185740696 185740696 AACACTAACTCAGCCCAACACTAACTCAGCCCAACATTAACTCAGCCCAACATTAACTCAGCCCA AACACTAACTCAGCCCAACACTAACTCAGCCCCACATTAACTCAGCCCAACATTAACTCAGCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185740691..185740778 26863196 MeRIP-seq:(Medium) rs1336462706 Functional Loss SNV dbSNP153 33..33 33 - - - 100042 RMVar_ID_100042 Human_SNP_ID_217359683 m1A Human chr4 - 185743698 185743698 185743698 ATCTGAATCAGGAGGAGGAGGGGCTCACCATCAGAGTCTTAGTTTGCCCTGTCCTTCCACTCATT ATCTGAATCAGGAGGAGGAGGGGCTCACCATCGGAGTCTTAGTTTGCCCTGTCCTTCCACTCATT T C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185743696..185743991 26863196 MeRIP-seq:(Medium) rs1280758976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941139 RMVar_hsa_circ_324587,RMVar_hsa_circ_365326,RMVar_hsa_circ_358337 100043 RMVar_ID_100043 Human_SNP_ID_217359687 m1A Human chr4 - 185743715 185743715 185743715 AAGAGGAGGAAGAAATCATCTGAATCAGGAGGAGGAGGGGCTCACCATCAGAGTCTTAGTTTGCC AAGAGGAGGAAGAAATCATCTGAATCAGGAGGGGGAGGGGCTCACCATCAGAGTCTTAGTTTGCC T C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185743674..185743998 26863196 MeRIP-seq:(Medium) rs1037957164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941139 RMVar_hsa_circ_324587,RMVar_hsa_circ_365326,RMVar_hsa_circ_358337 100044 RMVar_ID_100044 Human_SNP_ID_217359688 m1A Human chr4 - 185743715 185743715 185743715 AAGAGGAGGAAGAAATCATCTGAATCAGGAGGAGGAGGGGCTCACCATCAGAGTCTTAGTTTGCC AAGAGGAGGAAGAAATCATCTGAATCAGGAGGCGGAGGGGCTCACCATCAGAGTCTTAGTTTGCC T G SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185743674..185743998 26863196 MeRIP-seq:(Medium) rs1037957164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_941139 RMVar_hsa_circ_324587,RMVar_hsa_circ_365326,RMVar_hsa_circ_358337 100045 RMVar_ID_100045 Human_SNP_ID_217380423 m1A Human chr4 + 185827062 185827048 185827063 TCACCACCATCATCACCACCATCACCATCATCATCATCACCATCATCATCACCATCATCACCATC TCACCACCATCATCACCAC_______________CATCACCATCATCATCACCATCATCACCATC CCATCACCATCATCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:185827002..185827135 26863196 MeRIP-seq:(Medium) rs1478016468 Functional Loss DEL dbSNP153 20..34 33 - - - 100046 RMVar_ID_100046 Human_SNP_ID_217380426 m1A Human chr4 - 185827060 185827054 185827060 TGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTGGTGATGATGGTGGTGATG TGGTGATGATGGTGATGATGATGGTGATGATG______GTGATGGTGGTGATGATGGTGGTGATG CCATCAT C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185827019..185827102 26863196 MeRIP-seq:(Medium) rs1282181628 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_327968 100047 RMVar_ID_100047 Human_SNP_ID_217380427 m1A Human chr4 - 185827060 185827054 185827060 TGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTGGTGATGATGGTGGTGATG TGGTGATGATGGTGATGATGATGGTGATGATG___ATGGTGATGGTGGTGATGATGGTGGTGATG CCATCAT CCAT SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185827019..185827102 26863196 MeRIP-seq:(Medium) rs1282181628 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_327968 100048 RMVar_ID_100048 Human_SNP_ID_217380434 m1A Human chr4 - 185827060 185827060 185827060 TGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTGGTGATGATGGTGGTGATG TGGTGATGATGGTGATGATGATGGTGATGATGGTGATGGTGATGGTGGTGATGATGGTGGTGATG T C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:185827019..185827102 26863196 MeRIP-seq:(Medium) rs1308859070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327968 100049 RMVar_ID_100049 Human_SNP_ID_217380443 m1A Human chr4 - 185827078 185827069 185827078 CGATGATGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTG CGATGATGGTGATGATGATGGTGATGATGGTG_________GTGATGATGATGATGGTGATGGTG CCATCATCAT C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185827033..185827332 26863196 MeRIP-seq:(Medium) rs144017246 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_327968 100050 RMVar_ID_100050 Human_SNP_ID_217380444 m1A Human chr4 - 185827078 185827069 185827078 CGATGATGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTG CGATGATGGTGATGATGATGGTGATGATGGTG______ATGGTGATGATGATGATGGTGATGGTG CCATCATCAT CCAT SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185827033..185827332 26863196 MeRIP-seq:(Medium) rs144017246 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_327968 100051 RMVar_ID_100051 Human_SNP_ID_217380445 m1A Human chr4 - 185827078 185827069 185827078 CGATGATGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTG CGATGATGGTGATGATGATGGTGATGATGGTG___ATGATGGTGATGATGATGATGGTGATGGTG CCATCATCAT CCATCAT SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185827033..185827332 26863196 MeRIP-seq:(Medium) rs144017246 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_327968 100052 RMVar_ID_100052 Human_SNP_ID_217380455 m1A Human chr4 - 185827078 185827078 185827078 CGATGATGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGGTG CGATGATGGTGATGATGATGGTGATGATGGTGGTGATGATGGTGATGATGATGATGGTGATGGTG T C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:185827033..185827332 26863196 MeRIP-seq:(Medium) rs796524946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327968 100053 RMVar_ID_100053 Human_SNP_ID_217380645 m1A Human chr4 + 185827314 185827312 185827315 TCATCACCATCATCATCATCACCATCATCACCATCATCACCATCATCATCATCATCATCATCATC TCATCACCATCATCATCATCACCATCATCAC___CATCACCATCATCATCATCATCATCATCATC CCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:185827263..185827352 26863196 MeRIP-seq:(Medium) rs139013219 Functional Loss DEL dbSNP153 32..34 33 - - - 100054 RMVar_ID_100054 Human_SNP_ID_217452539 m1A Human chr4 - 186104772 186104757 186104773 GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCAGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCC________________GCCGCCCGCCGCCCGCGG CGGGCGGCGGGCGTCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186104725..186104905 26863196 MeRIP-seq:(Medium) rs1177700805 Functional Loss DEL dbSNP153 32..47 33 - - - 100055 RMVar_ID_100055 Human_SNP_ID_217452552 m1A Human chr4 - 186104772 186104764 186104773 GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCAGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCC_________GCCGCCCGCCGCCCGCCGCCCGCGG CGGGCGTCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186104725..186104905 26863196 MeRIP-seq:(Medium) rs898009919 Functional Loss DEL dbSNP153 32..40 33 - - - 100056 RMVar_ID_100056 Human_SNP_ID_217452555 m1A Human chr4 - 186104772 186104768 186104773 GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCAGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCC_____GCCCGCCGCCCGCCGCCCGCCGCCCGCGG CGTCTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186104725..186104905 26863196 MeRIP-seq:(Medium) rs1227279928 Functional Loss DEL dbSNP153 32..36 33 - - - 100057 RMVar_ID_100057 Human_SNP_ID_217452560 m1A Human chr4 - 186104772 186104771 186104773 GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCAGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCC__GACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG CTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186104725..186104905 26863196 MeRIP-seq:(Medium) rs1363560246 Functional Loss DEL dbSNP153 32..33 33 - - - 100058 RMVar_ID_100058 Human_SNP_ID_217452562 m1A Human chr4 - 186104772 186104772 186104772 GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCAGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG GAGCCCCGGGAAGCGCGGCCGCCGCCCGCCCCCGACGCCCGCCGCCCGCCGCCCGCCGCCCGCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186104725..186104905 26863196 MeRIP-seq:(Medium) rs1398549563 Functional Loss SNV dbSNP153 33..33 33 - - - 100059 RMVar_ID_100059 Human_SNP_ID_217584007 m1A Human chr4 - 186599986 186599986 186599986 AGCTATGCACACATCGAAGAGTCGGTGGATGTATCTCCAGGCTGCTTCCTGACGGCCACGGAAGA AGCTATGCACACATCGAAGAGTCGGTGGATGTGTCTCCAGGCTGCTTCCTGACGGCCACGGAAGA T C FAT1 Ensembl:ENSG00000083857 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:186599935..186601294 32194978 MeRIP-seq:(Medium) rs1244803589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70752,Human_RBP_ID_1975620,Human_RBP_ID_3735245,Human_RBP_ID_4798508,Human_RBP_ID_8878549,Human_RBP_ID_9303641,Human_RBP_ID_18032958 Human_Splice_Rec_629757,Human_Splice_Rec_629807 RMVar_hsa_circ_8012,RMVar_hsa_circ_21185,RMVar_hsa_circ_110292,RMVar_hsa_circ_318542,RMVar_hsa_circ_347240,RMVar_hsa_circ_94233,RMVar_hsa_circ_229885,RMVar_hsa_circ_229886,RMVar_hsa_circ_106313,RMVar_hsa_circ_79043,RMVar_hsa_circ_99456,RMVar_hsa_circ_229888,RMVar_hsa_circ_229889,RMVar_hsa_circ_96709,RMVar_hsa_circ_229890,RMVar_hsa_circ_229891,RMVar_hsa_circ_48655 100060 RMVar_ID_100060 Human_SNP_ID_217585349 m1A Human chr4 - 186604533 186604533 186604533 CCAGTGGGCTTCAGCGTGCTGCAGCTGGTAGTAACAGATGAGGATTCTTCCCATAACGGTCCACC CCAGTGGGCTTCAGCGTGCTGCAGCTGGTAGTGACAGATGAGGATTCTTCCCATAACGGTCCACC T C FAT1 Ensembl:ENSG00000083857 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:186604482..186609197 32194978 MeRIP-seq:(Medium) rs1215746069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1637046,Human_RBP_ID_8878602,Human_RBP_ID_17523544 Human_Splice_Rec_629748,Human_Splice_Rec_629798 RMVar_hsa_circ_110292,RMVar_hsa_circ_318542,RMVar_hsa_circ_347240,RMVar_hsa_circ_94233,RMVar_hsa_circ_229885,RMVar_hsa_circ_229886,RMVar_hsa_circ_106313,RMVar_hsa_circ_99456,RMVar_hsa_circ_229889,RMVar_hsa_circ_96709,RMVar_hsa_circ_229892,RMVar_hsa_circ_50402,RMVar_hsa_circ_229890,RMVar_hsa_circ_229891,RMVar_hsa_circ_89366,RMVar_hsa_circ_349279,RMVar_hsa_circ_371818,RMVar_hsa_circ_229893,RMVar_hsa_circ_229894,RMVar_hsa_circ_85276 100061 RMVar_ID_100061 Human_SNP_ID_217587071 m1A Human chr4 + 186609975 186609975 186609975 TCAGTGGCCTCTACTGTTAGGTAATACTCATGAGAGCTCTCATAATCCAGATTCTCAATGATAAA TCAGTGGCCTCTACTGTTAGGTAATACTCATGGGAGCTCTCATAATCCAGATTCTCAATGATAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:186609926..186611391 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 100062 RMVar_ID_100062 Human_SNP_ID_217594980 m1A Human chr4 - 186636728 186636728 186636728 CCAGACGGGAGCCGCTCTATCACGTCATAGCCACCGACAAGGATGAGGGCCCCAATGCAGAAATC CCAGACGGGAGCCGCTCTATCACGTCATAGCCGCCGACAAGGATGAGGGCCCCAATGCAGAAATC T C FAT1 Ensembl:ENSG00000083857 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:186636591..186636791 32194978 MeRIP-seq:(Medium) rs1391378491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70812,Human_RBP_ID_942349,Human_RBP_ID_4780568,Human_RBP_ID_9396831,Human_RBP_ID_18032967,Human_RBP_ID_22400650 Human_miRNA_ID_2489872,Human_miRNA_ID_2751957 RMVar_hsa_circ_318542,RMVar_hsa_circ_347240,RMVar_hsa_circ_99456,RMVar_hsa_circ_96709,RMVar_hsa_circ_1950,RMVar_hsa_circ_50402,RMVar_hsa_circ_229890,RMVar_hsa_circ_229891,RMVar_hsa_circ_371818,RMVar_hsa_circ_229893,RMVar_hsa_circ_77952,RMVar_hsa_circ_229897,RMVar_hsa_circ_76792,RMVar_hsa_circ_229896,RMVar_hsa_circ_91761,RMVar_hsa_circ_98954,RMVar_hsa_circ_229900,RMVar_hsa_circ_123877,RMVar_hsa_circ_29149,RMVar_hsa_circ_229901,RMVar_hsa_circ_116075,RMVar_hsa_circ_229905,RMVar_hsa_circ_229907,RMVar_hsa_circ_99938,RMVar_hsa_circ_229906,RMVar_hsa_circ_35814,RMVar_hsa_circ_22741,RMVar_hsa_circ_276553,RMVar_hsa_circ_229908,RMVar_hsa_circ_100645,RMVar_hsa_circ_324743,RMVar_hsa_circ_46488,RMVar_hsa_circ_94957,RMVar_hsa_circ_229909,RMVar_hsa_circ_229910,RMVar_hsa_circ_331853,RMVar_hsa_circ_51338,RMVar_hsa_circ_41332,RMVar_hsa_circ_229911,RMVar_hsa_circ_37021,RMVar_hsa_circ_78815,RMVar_hsa_circ_229912 100063 RMVar_ID_100063 Human_SNP_ID_217610350 m1A Human chr4 - 186694023 186694023 186694023 GTGAGATGTTGAGTTTTGTGAGAAATAGGAAGATGGTGGTTGGATTAGTAGATGAGAGGCAGGTT GTGAGATGTTGAGTTTTGTGAGAAATAGGAAGGTGGTGGTTGGATTAGTAGATGAGAGGCAGGTT T C FAT1 Ensembl:ENSG00000083857 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:186693893..186694243 26863196 MeRIP-seq:(Medium) rs970970662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318542,RMVar_hsa_circ_99456,RMVar_hsa_circ_229890,RMVar_hsa_circ_371818,RMVar_hsa_circ_229893,RMVar_hsa_circ_229897,RMVar_hsa_circ_76792,RMVar_hsa_circ_91761,RMVar_hsa_circ_98954,RMVar_hsa_circ_229900,RMVar_hsa_circ_229901,RMVar_hsa_circ_229907,RMVar_hsa_circ_99938,RMVar_hsa_circ_35814,RMVar_hsa_circ_22741,RMVar_hsa_circ_51338,RMVar_hsa_circ_342540,RMVar_hsa_circ_229914,RMVar_hsa_circ_281468 100064 RMVar_ID_100064 Human_SNP_ID_217679069 m1A Human chr4 + 186960981 186960981 186960981 TGGAAGAGGCAGGCGACATGCGAGTGCTGGAGAGGAACCCGGGATGCCACCATTTCACATGAAGA TGGAAGAGGCAGGCGACATGCGAGTGCTGGAGGGGAACCCGGGATGCCACCATTTCACATGAAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:186960936..186961050 26863196 MeRIP-seq:(Medium) rs1378333088 Functional Loss SNV dbSNP153 33..33 33 - - - 100065 RMVar_ID_100065 Human_SNP_ID_217975174 m1A Human chr4 + 188109461 188109461 188109461 GACCACACCCGGCTAATTTTTGTATTTTTTGTAGAGACGGGGTTTCAGTATTTTTCCCAGGCTGG GACCACACCCGGCTAATTTTTGTATTTTTTGTGGAGACGGGGTTTCAGTATTTTTCCCAGGCTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:188109411..188109537 26863196 MeRIP-seq:(Medium) rs1361901094 Functional Loss SNV dbSNP153 33..33 33 - - - 100066 RMVar_ID_100066 Human_SNP_ID_218087123 m1A Human chr4 + 188498597 188498597 188498597 AGGGGAGGGTGACTAGCCGGAAGACTTGGAGAAAGTGGAAGATGAAGAAAATCCTTTGAGCGGGG AGGGGAGGGTGACTAGCCGGAAGACTTGGAGAGAGTGGAAGATGAAGAAAATCCTTTGAGCGGGG A G LINC01060 Ensembl:ENSG00000249378 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:188498551..188498648 26863196 MeRIP-seq:(Medium) rs750886642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2839464,Human_RBP_ID_5608430 100067 RMVar_ID_100067 Human_SNP_ID_218486604 m1A Human chr4 - 189940895 189940895 189940895 AACAGAAGCGGACGCGAAATAAACACTCCCTGACAGCCTACGTCTCTGTAGAACCCGCCTCCGTC AACAGAAGCGGACGCGAAATAAACACTCCCTGGCAGCCTACGTCTCTGTAGAACCCGCCTCCGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:189940883..189941841 26863196 MeRIP-seq:(Medium) rs567441570 Functional Loss SNV dbSNP153 33..33 33 - - - 100068 RMVar_ID_100068 Human_SNP_ID_218486611 m1A Human chr4 - 189940907 189940907 189940907 GGGGCGCGGAGAAACAGAAGCGGACGCGAAATAAACACTCCCTGACAGCCTACGTCTCTGTAGAA GGGGCGCGGAGAAACAGAAGCGGACGCGAAATCAACACTCCCTGACAGCCTACGTCTCTGTAGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:189940897..189941024;chr4:189940897..189941046 26863196 MeRIP-seq:(Medium) rs1473426413 Functional Loss SNV dbSNP153 33..33 33 - - - 100069 RMVar_ID_100069 Human_SNP_ID_218486616 m1A Human chr4 - 189940916 189940916 189940916 GGCAGCACAGGGGCGCGGAGAAACAGAAGCGGACGCGAAATAAACACTCCCTGACAGCCTACGTC GGCAGCACAGGGGCGCGGAGAAACAGAAGCGGTCGCGAAATAAACACTCCCTGACAGCCTACGTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:189940903..189941021 26863196 MeRIP-seq:(Medium) rs555385653 Functional Loss SNV dbSNP153 33..33 33 - - - 100070 RMVar_ID_100070 Human_SNP_ID_218486683 m1A Human chr4 + 189940980 189940980 189940980 CCCGACTCACATACTCGTCCAGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTTCCCGGAGCCATG CCCGACTCACATACTCGTCCAGAACCGGCCTCCGCCTCTCCGCGCAGAAGTTTCCCGGAGCCATG A C FRG1 Ensembl:ENSG00000109536 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:189940884..189941890 32194978 MeRIP-seq:(Medium) rs763802708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4780820,Human_RBP_ID_8882209,Human_RBP_ID_9334839,Human_RBP_ID_26349676 Human_Splice_Rec_630501,Human_Splice_Rec_630513,Human_Splice_Rec_630529,Human_Splice_Rec_630539,Human_Splice_Rec_630549 100071 RMVar_ID_100071 Human_SNP_ID_218486684 m1A Human chr4 + 189940980 189940980 189940980 CCCGACTCACATACTCGTCCAGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTTCCCGGAGCCATG CCCGACTCACATACTCGTCCAGAACCGGCCTCGGCCTCTCCGCGCAGAAGTTTCCCGGAGCCATG A G FRG1 Ensembl:ENSG00000109536 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:189940884..189941890 32194978 MeRIP-seq:(Medium) rs763802708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4780820,Human_RBP_ID_8882209,Human_RBP_ID_9334839,Human_RBP_ID_26349676 Human_Splice_Rec_630501,Human_Splice_Rec_630513,Human_Splice_Rec_630529,Human_Splice_Rec_630539,Human_Splice_Rec_630549 100072 RMVar_ID_100072 Human_SNP_ID_218487137 m1A Human chr4 + 189941991 189941991 189941991 CCTCTCGAGGAGTCTGGCCTCATGAAGATGCCAGAATAAATGGCAGGTTTATCCTGAATGAATGT CCTCTCGAGGAGTCTGGCCTCATGAAGATGCCGGAATAAATGGCAGGTTTATCCTGAATGAATGT A G FRG1 Ensembl:ENSG00000109536 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:189941987..189952220 32194978 MeRIP-seq:(Medium) rs893696432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_630502,Human_Splice_Rec_630503,Human_Splice_Rec_630531,Human_Splice_Rec_630540 100073 RMVar_ID_100073 Human_SNP_ID_218529745 m1A Human chr4 + 190067613 190067610 190067613 CTCTCCCCCTTCCTCTTCGTCTCTCCGGCCCCACCACCACCACCGCCACCACGCCCTCCCCCCCC CTCTCCCCCTTCCTCTTCGTCTCTCCGGCC___CCACCACCACCGCCACCACGCCCTCCCCCCCC CCCA C DBET Ensembl:ENSG00000281591 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:190067601..190067675;chr4:190067601..190067758 26863196 MeRIP-seq:(Medium) rs1560856374 Functional Loss DEL dbSNP153 31..33 33 - - - 100074 RMVar_ID_100074 Human_SNP_ID_218546913 m1A Human chr4 - 190122998 190122998 190122998 CTAACCCTAACCCTAACCCTACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACC CTAACCCTAACCCTAACCCTACCCTAACCCTAGCCCTAACCCTAACCCTAACCCTAACCCTAACC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:190122926..190123010 26863410 MeRIP-seq:(Medium) rs1560878520 Functional Loss SNV dbSNP153 33..33 33 - - - 100075 RMVar_ID_100075 Human_SNP_ID_486469215 m1A Human chr11 - 130069944 130069944 130069944 CCTCGCCGGGTCGCTCTAGCGCGCGGCTCTCAAGCTCACACACTCGGACTCCTCGCTTAGCACAC CCTCGCCGGGTCGCTCTAGCGCGCGGCTCTCAGGCTCACACACTCGGACTCCTCGCTTAGCACAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:130069901..130069975 26863196 MeRIP-seq:(Medium) rs1321136871 Functional Loss SNV dbSNP153 33..33 33 - - - 100076 RMVar_ID_100076 Human_SNP_ID_486469216 m1A Human chr11 + 130069947 130069945 130069947 TGCTAAGCGAGGAGTCCGAGTGTGTGAGCTTGAGAGCCGCGCGCTAGAGCGACCCGGCGAGGGAT TGCTAAGCGAGGAGTCCGAGTGTGTGAGCTT__GAGCCGCGCGCTAGAGCGACCCGGCGAGGGAT TGA T APLP2 Ensembl:ENSG00000084234 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:130069901..130070000 26863196 MeRIP-seq:(Medium) rs745666276 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_32099,Human_RBP_ID_227524,Human_RBP_ID_751977,Human_RBP_ID_807057,Human_RBP_ID_4153147,Human_RBP_ID_5235137,Human_RBP_ID_5313860,Human_RBP_ID_8774567,Human_RBP_ID_9276164,Human_RBP_ID_9321819,Human_RBP_ID_9364429,Human_RBP_ID_22433323,Human_RBP_ID_23493776 Human_Splice_Rec_1317248,Human_Splice_Rec_1317345 100077 RMVar_ID_100077 Human_SNP_ID_486469219 m1A Human chr11 + 130069949 130069949 130069949 CTAAGCGAGGAGTCCGAGTGTGTGAGCTTGAGAGCCGCGCGCTAGAGCGACCCGGCGAGGGATGG CTAAGCGAGGAGTCCGAGTGTGTGAGCTTGAGGGCCGCGCGCTAGAGCGACCCGGCGAGGGATGG A G APLP2 Ensembl:ENSG00000084234 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:130069851..130070128;chr11:130069876..130070118;chr11:130069851..130070130;chr11:130069876..130070100 26863196 MeRIP-seq:(Medium) rs1203208772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32099,Human_RBP_ID_227524,Human_RBP_ID_751977,Human_RBP_ID_807057,Human_RBP_ID_4153147,Human_RBP_ID_5235137,Human_RBP_ID_5313860,Human_RBP_ID_8774567,Human_RBP_ID_9276164,Human_RBP_ID_9321819,Human_RBP_ID_9364429,Human_RBP_ID_22433323,Human_RBP_ID_23493776 Human_Splice_Rec_1317248,Human_Splice_Rec_1317345 100078 RMVar_ID_100078 Human_SNP_ID_486479982 m1A Human chr11 + 130109370 130109370 130109370 AAAAGATGCATTCTGTCACATAGACCTGAATGACTGTTGCCTCTGTGCTAGCCTTCTTGGAGTAA AAAAGATGCATTCTGTCACATAGACCTGAATGTCTGTTGCCTCTGTGCTAGCCTTCTTGGAGTAA A T APLP2 Ensembl:ENSG00000084234 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:130109365..130109500 26863410 MeRIP-seq:(Medium) rs58832753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122218,RMVar_hsa_circ_154035 100079 RMVar_ID_100079 Human_SNP_ID_486480025 m1A Human chr11 + 130109455 130109455 130109455 TGGTAGGCTCTTGCAGCCAATGCCGGAACAGGATTTGCTGTTGCTGAGCCTCAAATCGCAATGTT TGGTAGGCTCTTGCAGCCAATGCCGGAACAGGGTTTGCTGTTGCTGAGCCTCAAATCGCAATGTT A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:130109426..130109525 26863196 MeRIP-seq:(Medium) rs1243118011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29518,Human_RBP_ID_391953,Human_RBP_ID_1455097,Human_RBP_ID_1776845,Human_RBP_ID_4153153,Human_RBP_ID_8347135,Human_RBP_ID_9322389,Human_RBP_ID_9363124,Human_RBP_ID_18604888,Human_RBP_ID_22434949,Human_RBP_ID_22889502,Human_RBP_ID_23493836,Human_RBP_ID_26317895 Human_Splice_Rec_1317250,Human_Splice_Rec_1317286,Human_Splice_Rec_1317318,Human_Splice_Rec_1317326,Human_Splice_Rec_1317330,Human_Splice_Rec_1317336,Human_Splice_Rec_1317340,Human_Splice_Rec_1317346,Human_Splice_Rec_1317356,Human_Splice_Rec_1317376,Human_Splice_Rec_1317384,Human_Splice_Rec_1317390,Human_Splice_Rec_1317420,Human_Splice_Rec_1317454,Human_Splice_Rec_1317478,Human_Splice_Rec_1317510,Human_Splice_Rec_1317542 Human_miRNA_ID_1979105,Human_miRNA_ID_1979106,Human_miRNA_ID_2269654,Human_miRNA_ID_2269655,Human_miRNA_ID_2882527,Human_miRNA_ID_2882528 RMVar_hsa_circ_4173,RMVar_hsa_circ_122218,RMVar_hsa_circ_271246,RMVar_hsa_circ_310737,RMVar_hsa_circ_364116,RMVar_hsa_circ_154035,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_287093,RMVar_hsa_circ_68761,RMVar_hsa_circ_70481,RMVar_hsa_circ_59650,RMVar_hsa_circ_154036 100080 RMVar_ID_100080 Human_SNP_ID_486483275 m1A Human chr11 + 130121784 130121784 130121784 GAAGATGAAGAGGAAGAGGAAGAGGAAGATGAAGAGGAAGACTATGATGTTTATAAAAGGTAACT GAAGATGAAGAGGAAGAGGAAGAGGAAGATGAGGAGGAAGACTATGATGTTTATAAAAGGTAACT A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:130121672..130121847 26863196 MeRIP-seq:(Medium) rs759811297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193871,Human_RBP_ID_806687,Human_RBP_ID_868574,Human_RBP_ID_1462017,Human_RBP_ID_1776851,Human_RBP_ID_3939955,Human_RBP_ID_4153176,Human_RBP_ID_6055618,Human_RBP_ID_8229297,Human_RBP_ID_9343857,Human_RBP_ID_9363136,Human_RBP_ID_17648883,Human_RBP_ID_17668859,Human_RBP_ID_18188645,Human_RBP_ID_18410691,Human_RBP_ID_18526334,Human_RBP_ID_22036043,Human_RBP_ID_22755190,Human_RBP_ID_22889511,Human_RBP_ID_23113057,Human_RBP_ID_23117914,Human_RBP_ID_23493858,Human_RBP_ID_24542610,Human_RBP_ID_24550997,Human_RBP_ID_26319385,Human_RBP_ID_27804128 Human_Splice_Rec_1317257,Human_Splice_Rec_1317293,Human_Splice_Rec_1317380,Human_Splice_Rec_1317381,Human_Splice_Rec_1317386,Human_Splice_Rec_1317387,Human_Splice_Rec_1317397,Human_Splice_Rec_1317427,Human_Splice_Rec_1317485,Human_Splice_Rec_1317517 Human_miRNA_ID_1135394,Human_miRNA_ID_1137910 RMVar_hsa_circ_4173,RMVar_hsa_circ_271246,RMVar_hsa_circ_310737,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_70481,RMVar_hsa_circ_59650,RMVar_hsa_circ_154039,RMVar_hsa_circ_53654,RMVar_hsa_circ_348136,RMVar_hsa_circ_1982,RMVar_hsa_circ_121334 100081 RMVar_ID_100081 Human_SNP_ID_486483442 m1A Human chr11 + 130122361 130122353 130122362 GGAAGACTTCACAGAAGCAGCTGTGGATGAGGATGATGAGGATGAGGAAGAAGGGGAGGAAGTGG GGAAGACTTCACAGAAGCAGCTGTG_________GATGAGGATGAGGAAGAAGGGGAGGAAGTGG GGATGAGGAT G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:130120725..130123654 32194978 MeRIP-seq:(Medium) rs1247990052 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_29524,Human_RBP_ID_193607,Human_RBP_ID_806422,Human_RBP_ID_868576,Human_RBP_ID_986335,Human_RBP_ID_1776852,Human_RBP_ID_2258960,Human_RBP_ID_3941365,Human_RBP_ID_4153183,Human_RBP_ID_6055621,Human_RBP_ID_8229298,Human_RBP_ID_9363141,Human_RBP_ID_17681583,Human_RBP_ID_17804844,Human_RBP_ID_18410545,Human_RBP_ID_22035583,Human_RBP_ID_22755191,Human_RBP_ID_22889513,Human_RBP_ID_23113148,Human_RBP_ID_23493860,Human_RBP_ID_24542611,Human_RBP_ID_26317900,Human_RBP_ID_27804131 Human_Splice_Rec_1317258,Human_Splice_Rec_1317294,Human_Splice_Rec_1317382,Human_Splice_Rec_1317388,Human_Splice_Rec_1317398,Human_Splice_Rec_1317428,Human_Splice_Rec_1317486,Human_Splice_Rec_1317518 Human_miRNA_ID_2998902 RMVar_hsa_circ_4173,RMVar_hsa_circ_271246,RMVar_hsa_circ_310737,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_70481,RMVar_hsa_circ_59650,RMVar_hsa_circ_154039,RMVar_hsa_circ_53654,RMVar_hsa_circ_348136,RMVar_hsa_circ_1982,RMVar_hsa_circ_121334 100082 RMVar_ID_100082 Human_SNP_ID_486483474 m1A Human chr11 + 130122456 130122456 130122456 TCAAAGGAGATGACTACAATGAGGAGAATCCTACTGAACCCGGCAGCGACGGCACCATGTCAGAC TCAAAGGAGATGACTACAATGAGGAGAATCCTGCTGAACCCGGCAGCGACGGCACCATGTCAGAC A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:130122406..130123753 32194978 MeRIP-seq:(Medium) rs936510985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870455,Human_RBP_ID_1776853,Human_RBP_ID_3941365,Human_RBP_ID_5165478,Human_RBP_ID_5549047,Human_RBP_ID_6055623,Human_RBP_ID_9274607,Human_RBP_ID_9363145,Human_RBP_ID_11562395,Human_RBP_ID_17463810,Human_RBP_ID_17804844,Human_RBP_ID_18410546,Human_RBP_ID_21915930,Human_RBP_ID_22754482,Human_RBP_ID_22789900,Human_RBP_ID_22895228,Human_RBP_ID_23113149,Human_RBP_ID_24543007,Human_RBP_ID_26317901,Human_RBP_ID_26887623,Human_RBP_ID_27199389,Human_RBP_ID_27410184,Human_RBP_ID_27804131 Human_Splice_Rec_1317259,Human_Splice_Rec_1317295,Human_Splice_Rec_1317399,Human_Splice_Rec_1317429,Human_Splice_Rec_1317487,Human_Splice_Rec_1317519 RMVar_hsa_circ_4173,RMVar_hsa_circ_271246,RMVar_hsa_circ_310737,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_70481,RMVar_hsa_circ_59650,RMVar_hsa_circ_154039,RMVar_hsa_circ_53654,RMVar_hsa_circ_348136,RMVar_hsa_circ_1982,RMVar_hsa_circ_121334 100083 RMVar_ID_100083 Human_SNP_ID_486484946 m1A Human chr11 + 130127827 130127827 130127827 TCAAGCTAAGAACCTCCCCAAAGCAGAGAGGCAGACTCTGATTCAGGTAAGATGCCTTCTCTGGG TCAAGCTAAGAACCTCCCCAAAGCAGAGAGGCTGACTCTGATTCAGGTAAGATGCCTTCTCTGGG A T APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:130127713..130127889 26863196 MeRIP-seq:(Medium) rs190317673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870457,Human_RBP_ID_9321822,Human_RBP_ID_9363150,Human_RBP_ID_22434098,Human_RBP_ID_22753964,Human_RBP_ID_26319394,Human_RBP_ID_27804132 Human_Splice_Rec_1317264,Human_Splice_Rec_1317265,Human_Splice_Rec_1317298,Human_Splice_Rec_1317299,Human_Splice_Rec_1317402,Human_Splice_Rec_1317403,Human_Splice_Rec_1317434,Human_Splice_Rec_1317435,Human_Splice_Rec_1317460,Human_Splice_Rec_1317461,Human_Splice_Rec_1317492,Human_Splice_Rec_1317493,Human_Splice_Rec_1317524,Human_Splice_Rec_1317525 Human_miRNA_ID_2455508 RMVar_hsa_circ_4173,RMVar_hsa_circ_310737,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_70481,RMVar_hsa_circ_59650,RMVar_hsa_circ_1982,RMVar_hsa_circ_154040,RMVar_hsa_circ_288767,RMVar_hsa_circ_317311,RMVar_hsa_circ_343561,RMVar_hsa_circ_154041,RMVar_hsa_circ_100836,RMVar_hsa_circ_154042 100084 RMVar_ID_100084 Human_SNP_ID_486485507 m1A Human chr11 + 130130088 130130088 130130088 GCCTTACGGCGTTATGTCCGTGCTGAGAACAAAGATCGCTTACATACCATCCGTCATTACCAGCA GCCTTACGGCGTTATGTCCGTGCTGAGAACAAGGATCGCTTACATACCATCCGTCATTACCAGCA A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:130129983..130130210 26863196 MeRIP-seq:(Medium) rs1003314123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29529,Human_RBP_ID_1161351,Human_RBP_ID_1776861,Human_RBP_ID_11562539,Human_RBP_ID_22379564,Human_RBP_ID_22753970,Human_RBP_ID_27410189 Human_Splice_Rec_1317268,Human_Splice_Rec_1317269,Human_Splice_Rec_1317302,Human_Splice_Rec_1317303,Human_Splice_Rec_1317406,Human_Splice_Rec_1317407,Human_Splice_Rec_1317438,Human_Splice_Rec_1317439,Human_Splice_Rec_1317464,Human_Splice_Rec_1317465,Human_Splice_Rec_1317496,Human_Splice_Rec_1317497,Human_Splice_Rec_1317528,Human_Splice_Rec_1317529 Human_miRNA_ID_1957154 RMVar_hsa_circ_4173,RMVar_hsa_circ_310737,RMVar_hsa_circ_364446,RMVar_hsa_circ_354934,RMVar_hsa_circ_70481,RMVar_hsa_circ_1982,RMVar_hsa_circ_154040,RMVar_hsa_circ_288767,RMVar_hsa_circ_317311,RMVar_hsa_circ_343561,RMVar_hsa_circ_154041,RMVar_hsa_circ_100836,RMVar_hsa_circ_154042,RMVar_hsa_circ_154044,RMVar_hsa_circ_349420 100085 RMVar_ID_100085 Human_SNP_ID_486486653 m1A Human chr11 - 130134713 130134713 130134713 TCCCCAGCTGTCCCTGGGGTGCTCCTTCTCCTACCCCGTCACCCCTTCAGTGCATACTCCCAACA TCCCCAGCTGTCCCTGGGGTGCTCCTTCTCCTCCCCCGTCACCCCTTCAGTGCATACTCCCAACA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:130134709..130134862 26863196 MeRIP-seq:(Medium) rs1353566884 Functional Loss SNV dbSNP153 33..33 33 - - - 100086 RMVar_ID_100086 Human_SNP_ID_486486721 m1A Human chr11 + 130134976 130134976 130134976 TGTTATGTGGGGATGTAGGATTTAGGTGAGGCAGAGGTCAGGCAGTAGGTCCAGGATTCGGGCCT TGTTATGTGGGGATGTAGGATTTAGGTGAGGCGGAGGTCAGGCAGTAGGTCCAGGATTCGGGCCT A G APLP2 Ensembl:ENSG00000084234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:130134974..130135094 26863196 MeRIP-seq:(Medium) rs938060902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6055652,Human_RBP_ID_11562642 RMVar_hsa_circ_4173,RMVar_hsa_circ_364446,RMVar_hsa_circ_70481,RMVar_hsa_circ_1982,RMVar_hsa_circ_317311,RMVar_hsa_circ_154041,RMVar_hsa_circ_100836,RMVar_hsa_circ_154042,RMVar_hsa_circ_58510,RMVar_hsa_circ_119902,RMVar_hsa_circ_154045 100087 RMVar_ID_100087 Human_SNP_ID_486486866 m1A Human chr11 + 130135566 130135566 130135566 CTTTCTGTCCCCTGCCCTGTCTTCATCAGATGAGCTCCTTCAGGAGCAGCGTGCAGATATGGACC CTTTCTGTCCCCTGCCCTGTCTTCATCAGATGGGCTCCTTCAGGAGCAGCGTGCAGATATGGACC A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1324495628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_870464,Human_RBP_ID_5168935,Human_RBP_ID_8774571,Human_RBP_ID_9364455,Human_RBP_ID_11562652,Human_RBP_ID_22434100,Human_RBP_ID_22753973,Human_RBP_ID_26319397 Human_Splice_Rec_1317272,Human_Splice_Rec_1317306,Human_Splice_Rec_1317410,Human_Splice_Rec_1317442,Human_Splice_Rec_1317468,Human_Splice_Rec_1317500,Human_Splice_Rec_1317532 RMVar_hsa_circ_4173,RMVar_hsa_circ_364446,RMVar_hsa_circ_70481,RMVar_hsa_circ_15452,RMVar_hsa_circ_1982,RMVar_hsa_circ_317311,RMVar_hsa_circ_154041,RMVar_hsa_circ_100836,RMVar_hsa_circ_154042,RMVar_hsa_circ_58510,RMVar_hsa_circ_119902,RMVar_hsa_circ_52255,RMVar_hsa_circ_154045 100088 RMVar_ID_100088 Human_SNP_ID_486489089 m1A Human chr11 + 130143416 130143416 130143416 ACAAGATGCAGAACCATGGCTATGAGAACCCCACCTACAAATACCTGGAGCAGATGCAGATTTAG ACAAGATGCAGAACCATGGCTATGAGAACCCCGCCTACAAATACCTGGAGCAGATGCAGATTTAG A G APLP2 Ensembl:ENSG00000084234 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:130143331..130143525 26863196 MeRIP-seq:(Medium) rs1354625575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29537,Human_RBP_ID_6055699,Human_RBP_ID_9000559,Human_RBP_ID_11562864,Human_RBP_ID_17649352,Human_RBP_ID_17792288,Human_RBP_ID_18188646,Human_RBP_ID_18410547,Human_RBP_ID_22035006,Human_RBP_ID_22434958,Human_RBP_ID_22753982,Human_RBP_ID_27199407,Human_RBP_ID_27410191,Human_RBP_ID_27805202 Human_Splice_Rec_1317282,Human_Splice_Rec_1317316,Human_Splice_Rec_1317418,Human_Splice_Rec_1317452,Human_Splice_Rec_1317476,Human_Splice_Rec_1317508,Human_Splice_Rec_1317540,Human_Splice_Rec_1317554,Human_Splice_Rec_1317558,Human_Splice_Rec_1317560 RMVar_hsa_circ_100836,RMVar_hsa_circ_154042,RMVar_hsa_circ_119902,RMVar_hsa_circ_154045 100089 RMVar_ID_100089 Human_SNP_ID_486489372 m1A Human chr11 + 130144396 130144396 130144396 ACCGGCCTTGTGACATTCACTCAGAGAAGACCACACCAAGGAGGCGGCCGCTGGCCCAGGAGAGA ACCGGCCTTGTGACATTCACTCAGAGAAGACCGCACCAAGGAGGCGGCCGCTGGCCCAGGAGAGA A G APLP2 Ensembl:ENSG00000084234 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1396080104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_392011,Human_RBP_ID_17235090,Human_RBP_ID_17681607,Human_RBP_ID_18248761,Human_RBP_ID_23493935 RMVar_hsa_circ_100836,RMVar_hsa_circ_154042,RMVar_hsa_circ_119902,RMVar_hsa_circ_154045 100090 RMVar_ID_100090 Human_SNP_ID_486500320 m1A Human chr11 + 130188354 130188354 130188354 TCCCTCTTCCCTCAGCGGACAGACCCAGGGCCACCTACTGAGTACACGAGGATCTCTTGGCCTCT TCCCTCTTCCCTCAGCGGACAGACCCAGGGCCTCCTACTGAGTACACGAGGATCTCTTGGCCTCT A T ST14 Ensembl:ENSG00000149418 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:130188331..130188422 26863196 MeRIP-seq:(Medium) rs1385988497 Functional Loss SNV dbSNP153 33..33 33 - - - 100091 RMVar_ID_100091 Human_SNP_ID_486528040 m1A Human chr11 - 130290445 130290445 130290445 GTCTTGGTGACCAGGTCTGTGTTAGGAGGAAAAGGGGAAGAGAAATTGTATTAGTTTTCTGTGGC GTCTTGGTGACCAGGTCTGTGTTAGGAGGAAAGGGGGAAGAGAAATTGTATTAGTTTTCTGTGGC T C ZBTB44 Ensembl:ENSG00000196323 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:130290441..130290526 26863410 MeRIP-seq:(Medium) rs779274378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86537,RMVar_hsa_circ_154057 100092 RMVar_ID_100092 Human_SNP_ID_486534559 m1A Human chr11 + 130314656 130314656 130314656 GGAGGGAAGCACCCCCAGCGCTCGGAGGGGCCAGAGGGGAGGAGCGAGGGGGCCCGGGAGCCGCG GGAGGGAAGCACCCCCAGCGCTCGGAGGGGCCCGAGGGGAGGAGCGAGGGGGCCCGGGAGCCGCG A C ZBTB44-DT,ZBTB44-DT:2,ZBTB44-DT:3,ZBTB44-DT:4,ZBTB44-DT:5,ZBTB44-DT:6 RNACentral:URS0000D588BE,RNACentral:URS0000D57504,RNACentral:URS0000D5B2F8,RNACentral:URS0000D58477,RNACentral:URS00008B25D9,RNACentral:URS0000D594A5 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:130314360..130314680 26863196 MeRIP-seq:(Medium) rs913002922 Functional Loss SNV dbSNP153 33..33 33 - - - 100093 RMVar_ID_100093 Human_SNP_ID_486534581 m1A Human chr11 - 130314711 130314711 130314711 GCGCTCCCCAAACAACCGCCTGCCCTCGGCCAACCGTCCCCAACGGTCGCCAGCGCGCGGCTCCC GCGCTCCCCAAACAACCGCCTGCCCTCGGCCAGCCGTCCCCAACGGTCGCCAGCGCGCGGCTCCC T C ZBTB44 Ensembl:ENSG00000196323 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:130314408..130314884 26863196 MeRIP-seq:(Medium) rs1479035106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86537,RMVar_hsa_circ_154057 100094 RMVar_ID_100094 Human_SNP_ID_486534593 m1A Human chr11 - 130314753 130314753 130314753 CCTTCCCCACCCCGCCCCGCTGGGAACACGCGAGCCGTCGCCGCGCTCCCCAAACAACCGCCTGC CCTTCCCCACCCCGCCCCGCTGGGAACACGCGCGCCGTCGCCGCGCTCCCCAAACAACCGCCTGC T G ZBTB44 Ensembl:ENSG00000196323 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:130261894..130314889 26863196 MeRIP-seq:(Medium) rs1288606911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17792386 100095 RMVar_ID_100095 Human_SNP_ID_486534632 m1A Human chr11 + 130314808 130314808 130314808 GTGGGGAAGGGGAAGGGGACTGAGGGGAGGGGAGGGGGAGGTTGGGAGGGAGCCGCCGCCGCGCG GTGGGGAAGGGGAAGGGGACTGAGGGGAGGGGGGGGGGAGGTTGGGAGGGAGCCGCCGCCGCGCG A G ZBTB44-DT,ZBTB44-DT:2,ZBTB44-DT:3,ZBTB44-DT:4,ZBTB44-DT:5,ZBTB44-DT:6 RNACentral:URS0000D588BE,RNACentral:URS0000D57504,RNACentral:URS0000D5B2F8,RNACentral:URS0000D58477,RNACentral:URS00008B25D9,RNACentral:URS0000D594A5 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:130314626..130314890 26863410 MeRIP-seq:(Medium) rs923870640 Functional Loss SNV dbSNP153 33..33 33 - - - 100096 RMVar_ID_100096 Human_SNP_ID_486534672 m1A Human chr11 - 130314863 130314858 130314864 CCCCCAAACAGGCTGGAGTGAGCGGAGCGGCAACGGCGGCGGCGCCGGCCGCACGCGCGCGGCGG CCCCCAAACAGGCTGGAGTGAGCGGAGCGGC______GGCGGCGCCGGCCGCACGCGCGCGGCGG CGCCGTT C ZBTB44 Ensembl:ENSG00000196323 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:130314778..130314873 26863410 MeRIP-seq:(Medium) rs1324234147 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_5489286 100097 RMVar_ID_100097 Human_SNP_ID_486684558 m1A Human chr11 - 130916397 130916397 130916397 CGGAGCGCAGTCGCCCAGGTTTACGGCGGCAGAGGGCCGAGGCTCCCGGAGAGGACCGCGATGAG CGGAGCGCAGTCGCCCAGGTTTACGGCGGCAGGGGGCCGAGGCTCCCGGAGAGGACCGCGATGAG T C SNX19 Ensembl:ENSG00000120451 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:130916346..130916414 26863196 MeRIP-seq:(Medium) rs545490890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4153749 100098 RMVar_ID_100098 Human_SNP_ID_487473121 m1A Human chr11 - 133901948 133901940 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG________GTGTGTTGTGTGGTTTGGTGTGTGT CACACACAT C IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1294807310 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_23494342 100099 RMVar_ID_100099 Human_SNP_ID_487473133 m1A Human chr11 - 133901948 133901943 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG_____TGTGTGTGTTGTGTGGTTTGGTGTGTGT ACACAT A IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1555082677 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_23494342 100100 RMVar_ID_100100 Human_SNP_ID_487473135 m1A Human chr11 - 133901948 133901944 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG____GTGTGTGTGTTGTGTGGTTTGGTGTGTGT CACAT C IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1379461132 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23494342 100101 RMVar_ID_100101 Human_SNP_ID_487473137 m1A Human chr11 - 133901948 133901945 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG___TGTGTGTGTGTTGTGTGGTTTGGTGTGTGT ACAT A IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1356955173 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_23494342 100102 RMVar_ID_100102 Human_SNP_ID_487473142 m1A Human chr11 - 133901948 133901946 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG__GTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT CAT C IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1227316278 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23494342 100103 RMVar_ID_100103 Human_SNP_ID_487473143 m1A Human chr11 - 133901948 133901947 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTG_TGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT AT A IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs1287167917 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23494342 100104 RMVar_ID_100104 Human_SNP_ID_487473146 m1A Human chr11 - 133901948 133901948 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTGTTGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT T A IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs957056909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23494342 100105 RMVar_ID_100105 Human_SNP_ID_487473147 m1A Human chr11 - 133901948 133901948 133901948 TGCATGTGTGTGATGCGGTGTGCATGTGTGTGATGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT TGCATGTGTGTGATGCGGTGTGCATGTGTGTGGTGTGTGTGTGTGTTGTGTGGTTTGGTGTGTGT T C IGSF9B Ensembl:ENSG00000080854 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:133901857..133902297 26863196 MeRIP-seq:(Medium) rs957056909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23494342 100106 RMVar_ID_100106 Human_SNP_ID_487474255 m1A Human chr11 + 133905626 133905624 133905626 CTTCCCCCAAGCGCATGGTTGTGGGACTAAGCACCTCAAAGGAGGGCACAGACCCCGCCAGCCTG CTTCCCCCAAGCGCATGGTTGTGGGACTAAG__CCTCAAAGGAGGGCACAGACCCCGCCAGCCTG GCA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:133905581..133905700 32194978 MeRIP-seq:(Medium) rs1181608621 Functional Loss DEL dbSNP153 32..33 33 - - - 100107 RMVar_ID_100107 Human_SNP_ID_487546943 m1A Human chr11 + 134150367 134150367 134150367 GAGGCCACCCAGAAGCCCTCAGATGTACATACACAGATGCCAGTCAGCTCCTGGGGTTGCGCCAG GAGGCCACCCAGAAGCCCTCAGATGTACATACGCAGATGCCAGTCAGCTCCTGGGGTTGCGCCAG A G JAM3 Ensembl:ENSG00000166086 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:134150266..134150465 32194978 MeRIP-seq:(Medium) rs1409344575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_392289,Human_RBP_ID_17347963 Human_miRNA_ID_2292222,Human_miRNA_ID_2357566,Human_miRNA_ID_3060006 RMVar_hsa_circ_105882,RMVar_hsa_circ_154101 100108 RMVar_ID_100108 Human_SNP_ID_487547981 m1A Human chr11 - 134152944 134152944 134152944 CTCCGAAAGACCCCTCTGAAAACAGCCAACTAAACAGCGCCTCCCACCAGTGTCCAGGCAGGCAG CTCCGAAAGACCCCTCTGAAAACAGCCAACTAGACAGCGCCTCCCACCAGTGTCCAGGCAGGCAG T C NCAPD3 Ensembl:ENSG00000151503 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:134152893..134153005 26863196 MeRIP-seq:(Medium) rs747180381 Functional Loss SNV dbSNP153 33..33 33 - - - 100109 RMVar_ID_100109 Human_SNP_ID_487548335 m1A Human chr11 - 134153565 134153565 134153565 CCAGCCGAGTGCCTGAGGGCTGCGGGTCAGAGAAGGGGGTCAGAGAGACGGAAAGGAGCATCCCC CCAGCCGAGTGCCTGAGGGCTGCGGGTCAGAGGAGGGGGTCAGAGAGACGGAAAGGAGCATCCCC T C NCAPD3 Ensembl:ENSG00000151503 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:134153548..134153750 26863196 MeRIP-seq:(Medium) rs1044199764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6056663,Human_RBP_ID_11565203,Human_RBP_ID_22572024,Human_RBP_ID_23267823,Human_RBP_ID_24875735 RMVar_hsa_circ_76518,RMVar_hsa_circ_154102 100110 RMVar_ID_100110 Human_SNP_ID_487548382 m1A Human chr11 - 134153675 134153675 134153675 TGAGCCACAGTAGGAGGTGTAGTAAGTGGGACAGGGCGGTCACCGGGACAGGGGCAATGATGGAA TGAGCCACAGTAGGAGGTGTAGTAAGTGGGACGGGGCGGTCACCGGGACAGGGGCAATGATGGAA T C NCAPD3 Ensembl:ENSG00000151503 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:134153488..134153887 26863196 MeRIP-seq:(Medium) rs990159460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226767,Human_RBP_ID_808820,Human_RBP_ID_6056665,Human_RBP_ID_11565208,Human_RBP_ID_18933073 RMVar_hsa_circ_76518,RMVar_hsa_circ_154102 100111 RMVar_ID_100111 Human_SNP_ID_487570095 m1A Human chr11 - 134218304 134218304 134218304 TCTGCAGAGGAGCAGTCACATGTAGGGAGTGCAGGGTCACTGACGCCCAGACTAGACAGCAGCCA TCTGCAGAGGAGCAGTCACATGTAGGGAGTGCGGGGTCACTGACGCCCAGACTAGACAGCAGCCA T C NCAPD3 Ensembl:ENSG00000151503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134218298..134218401 26863196 MeRIP-seq:(Medium) rs910588056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11566654 RMVar_hsa_circ_378746,RMVar_hsa_circ_18625 100112 RMVar_ID_100112 Human_SNP_ID_487570137 m1A Human chr11 - 134218463 134218461 134218464 TCAGGAGATCCTTGGGAAGTTTAACAGGTAGTAGAAATGTGAGACCAGGAGAGAGAAGAGAGTTC TCAGGAGATCCTTGGGAAGTTTAACAGGTAG___AAATGTGAGACCAGGAGAGAGAAGAGAGTTC TCTA T NCAPD3 Ensembl:ENSG00000151503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134218462..134218527 26863196 MeRIP-seq:(Medium) rs375465209 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_378746,RMVar_hsa_circ_18625 100113 RMVar_ID_100113 Human_SNP_ID_487570138 m1A Human chr11 - 134218463 134218463 134218463 TCAGGAGATCCTTGGGAAGTTTAACAGGTAGTAGAAATGTGAGACCAGGAGAGAGAAGAGAGTTC TCAGGAGATCCTTGGGAAGTTTAACAGGTAGTGGAAATGTGAGACCAGGAGAGAGAAGAGAGTTC T C NCAPD3 Ensembl:ENSG00000151503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134218462..134218527 26863196 MeRIP-seq:(Medium) rs1203151783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378746,RMVar_hsa_circ_18625 100114 RMVar_ID_100114 Human_SNP_ID_487570715 m1A Human chr11 - 134220675 134220675 134220675 GGAACTGGATTTCACAGAGACTGAGCCTTTGGATCCCAGCATAGAAGCAGAGATCATAGAGACTG GGAACTGGATTTCACAGAGACTGAGCCTTTGGGTCCCAGCATAGAAGCAGAGATCATAGAGACTG T C NCAPD3 Ensembl:ENSG00000151503 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:134220626..134223129 26863196 MeRIP-seq:(Medium) rs1200615140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1455256,Human_RBP_ID_1777044,Human_RBP_ID_2259488,Human_RBP_ID_4185499,Human_RBP_ID_5461201,Human_RBP_ID_6056915,Human_RBP_ID_9363173,Human_RBP_ID_11566682,Human_RBP_ID_18605179 Human_Splice_Rec_1318542,Human_Splice_Rec_1318608,Human_Splice_Rec_1318674,Human_Splice_Rec_1318760,Human_Splice_Rec_1318776,Human_Splice_Rec_1318780 RMVar_hsa_circ_378746,RMVar_hsa_circ_18625 100115 RMVar_ID_100115 Human_SNP_ID_487571403 m1A Human chr11 + 134223334 134223334 134223334 GGAGCGGGGCTGCCCTGAGACACCTCAGAGGCAGGACAGTGGTAGTGGGCATGAAAGGGGAAGCA GGAGCGGGGCTGCCCTGAGACACCTCAGAGGCCGGACAGTGGTAGTGGGCATGAAAGGGGAAGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134223330..134223421 26863196 MeRIP-seq:(Medium) rs1324711535 Functional Loss SNV dbSNP153 33..33 33 - - - 100116 RMVar_ID_100116 Human_SNP_ID_487571644 m1A Human chr11 + 134223907 134223901 134223908 CCAGCGGACACCAGGGCTGCAGGCCGCTACCAAGGCCCCGCAACGCCACCATGATCCCAGGGCAC CCAGCGGACACCAGGGCTGCAGGCCGC_______GCCCCGCAACGCCACCATGATCCCAGGGCAC CTACCAAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134223826..134223975 26863196 MeRIP-seq:(Medium) rs984853789 Functional Loss DEL dbSNP153 28..34 33 - - - 100117 RMVar_ID_100117 Human_SNP_ID_487571650 m1A Human chr11 + 134223906 134223906 134223906 TCCAGCGGACACCAGGGCTGCAGGCCGCTACCAAGGCCCCGCAACGCCACCATGATCCCAGGGCA TCCAGCGGACACCAGGGCTGCAGGCCGCTACCGAGGCCCCGCAACGCCACCATGATCCCAGGGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:134223851..134223950 26863196 MeRIP-seq:(Medium) rs937724964 Functional Loss SNV dbSNP153 33..33 33 - - - 100118 RMVar_ID_100118 Human_SNP_ID_487571661 m1A Human chr11 + 134223916 134223916 134223916 ACCAGGGCTGCAGGCCGCTACCAAGGCCCCGCAACGCCACCATGATCCCAGGGCACCGGCTCGCC ACCAGGGCTGCAGGCCGCTACCAAGGCCCCGCCACGCCACCATGATCCCAGGGCACCGGCTCGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:134223829..134223975;chr11:134223835..134223925 26863196 MeRIP-seq:(Medium) rs778042319 Functional Loss SNV dbSNP153 33..33 33 - - - 100119 RMVar_ID_100119 Human_SNP_ID_487575316 m1A Human chr11 + 134237416 134237416 134237416 CAGAGGGCTATCAGGAGGAAGAAATGATCTGGAGATAAGGTGATTCATCCAGCTCTAGAGGGCAG CAGAGGGCTATCAGGAGGAAGAAATGATCTGGGGATAAGGTGATTCATCCAGCTCTAGAGGGCAG A G VPS26B Ensembl:ENSG00000151502 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134237412..134237488 26863196 MeRIP-seq:(Medium) rs920000695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114768,RMVar_hsa_circ_154117,RMVar_hsa_circ_362823 100120 RMVar_ID_100120 Human_SNP_ID_487575376 m1A Human chr11 + 134237702 134237702 134237702 GCGCCTCTGTGGAACCGCGGGAAGAGTGTTTCAAGGAAGAAGTGTTTCACGGGACGCAGAATCAA GCGCCTCTGTGGAACCGCGGGAAGAGTGTTTCGAGGAAGAAGTGTTTCACGGGACGCAGAATCAA A G VPS26B Ensembl:ENSG00000151502 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134237687..134237918 26863196 MeRIP-seq:(Medium) rs996562015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114768,RMVar_hsa_circ_154117,RMVar_hsa_circ_362823 100121 RMVar_ID_100121 Human_SNP_ID_487575394 m1A Human chr11 - 134237773 134237773 134237773 ACCACCCAACAGAAACCGCTCGCCTCGAGGTCAGTAACCCATGGCCTCCCAGCTGCCAAATCCAG ACCACCCAACAGAAACCGCTCGCCTCGAGGTCGGTAACCCATGGCCTCCCAGCTGCCAAATCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:134237745..134237948 26863196 MeRIP-seq:(Medium) rs924177806 Functional Loss SNV dbSNP153 33..33 33 - - - 100122 RMVar_ID_100122 Human_SNP_ID_487577540 m1A Human chr11 - 134245792 134245792 134245792 GGATGCTACCTCTTCTATCCCACATCGGCCGCAGAATCCCAAGGAGAGACTGCTTCCCACCCCAA GGATGCTACCTCTTCTATCCCACATCGGCCGCGGAATCCCAAGGAGAGACTGCTTCCCACCCCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:134245747..134245947 32194978 MeRIP-seq:(Medium) rs1479502483 Functional Loss SNV dbSNP153 33..33 33 - - - 100123 RMVar_ID_100123 Human_SNP_ID_487577888 m1A Human chr11 + 134247131 134247131 134247131 GAGACTGGAGGGAGAGGCATTTTGGGTAGCCTAGGAGGGCGACTGGCGGCAGCAGAACCGAGGAA GAGACTGGAGGGAGAGGCATTTTGGGTAGCCTGGGAGGGCGACTGGCGGCAGCAGAACCGAGGAA A G VPS26B Ensembl:ENSG00000151502 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:134247082..134247161 26863196 MeRIP-seq:(Medium) rs1031978360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409115 RMVar_hsa_circ_114768,RMVar_hsa_circ_154117,RMVar_hsa_circ_117896,RMVar_hsa_circ_154119 100124 RMVar_ID_100124 Human_SNP_ID_487579872 m1A Human chr11 - 134253624 134253624 134253624 CCGCCGGGCAGGCAGCCGAGGCGCGCCCCGAAACGCCGGCAGCCGCTCCACAGCATAGCCGCCGC CCGCCGGGCAGGCAGCCGAGGCGCGCCCCGAAGCGCCGGCAGCCGCTCCACAGCATAGCCGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134253586..134253680 26863196 MeRIP-seq:(Medium) rs748277154 Functional Loss SNV dbSNP153 33..33 33 - - - 100125 RMVar_ID_100125 Human_SNP_ID_487580004 m1A Human chr11 - 134253913 134253912 134253913 GGACCCGGGCAGGGGTGACGGGCCAGATGGGGACCCGGATGGTGGTGACCGACCGGAGGGGGCAG GGACCCGGGCAGGGGTGACGGGCCAGATGGGG_CCCGGATGGTGGTGACCGACCGGAGGGGGCAG GT G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:134253839..134254020 26863196 MeRIP-seq:(Medium) rs555113446 Functional Loss DEL dbSNP153 33..33 33 - - - 100126 RMVar_ID_100126 Human_SNP_ID_487580716 m1A Human chr11 + 134256525 134256525 134256525 CCTTGTTGGCAACACTGACCCTGTCCTAGAACAGTATATGCAATCCTGCCCACAGCTTCCATGGG CCTTGTTGGCAACACTGACCCTGTCCTAGAACGGTATATGCAATCCTGCCCACAGCTTCCATGGG A G ACAD8 Ensembl:ENSG00000151498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:134256524..134256589 26863196 MeRIP-seq:(Medium) rs1478277861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11567004 RMVar_hsa_circ_33345 100127 RMVar_ID_100127 Human_SNP_ID_487585840 m1A Human chr11 - 134276116 134276116 134276116 AGCGGCCCGAGCACAGCCTCACAGCAGATGCGAGCGCGGCGGGCGCTTTGGTGACGAAGTAGCGG AGCGGCCCGAGCACAGCCTCACAGCAGATGCGGGCGCGGCGGGCGCTTTGGTGACGAAGTAGCGG T C lnc-THYN1-1-001 RNACentral:URS00008BE34D lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs2443557 Functional Loss SNV dbSNP153 33..33 33 - - - 100128 RMVar_ID_100128 Human_SNP_ID_487615978 m1A Human chr11 + 134382912 134382912 134382912 GCCGGTGGGGGTCAAACACCGTCTTCCAGCCGACCACCTTCCCTGCCCCGTTCACCCGTGGGGCC GCCGGTGGGGGTCAAACACCGTCTTCCAGCCGGCCACCTTCCCTGCCCCGTTCACCCGTGGGGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:134382861..134382982 26863196 MeRIP-seq:(Medium) rs768927813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154135 100129 RMVar_ID_100129 Human_SNP_ID_487712788 m1A Human chr11 + 134735527 134735527 134735527 GGGTTCGTGGGCAGAGTGGTGAGCGACGGAGAACTGGGGTTCGTGAGCAGAGTGGTGAGCGACGG GGGTTCGTGGGCAGAGTGGTGAGCGACGGAGAGCTGGGGTTCGTGAGCAGAGTGGTGAGCGACGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:134735478..134735565 26863196 MeRIP-seq:(Medium) rs569795111 Functional Loss SNV dbSNP153 33..33 33 - - - 100130 RMVar_ID_100130 Human_SNP_ID_536550281 m1A Human chr13 - 75335137 75335137 75335137 TAGGAGGCAGCATACTGGCAGAGGGAAGGCCCAGTGCGGGTGTCAGAGCCACAGTGGAGGGGAGC TAGGAGGCAGCATACTGGCAGAGGGAAGGCCCTGTGCGGGTGTCAGAGCCACAGTGGAGGGGAGC T A TBC1D4 Ensembl:ENSG00000136111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75335105..75335245 26863196 MeRIP-seq:(Medium) rs1307784507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24366793 RMVar_hsa_circ_80307,RMVar_hsa_circ_122517,RMVar_hsa_circ_110492,RMVar_hsa_circ_163748,RMVar_hsa_circ_163749,RMVar_hsa_circ_163750,RMVar_hsa_circ_340769,RMVar_hsa_circ_376436,RMVar_hsa_circ_374940,RMVar_hsa_circ_345233,RMVar_hsa_circ_163752,RMVar_hsa_circ_365213,RMVar_hsa_circ_57390,RMVar_hsa_circ_76499,RMVar_hsa_circ_163753,RMVar_hsa_circ_121596,RMVar_hsa_circ_30703,RMVar_hsa_circ_372599,RMVar_hsa_circ_163754,RMVar_hsa_circ_286260,RMVar_hsa_circ_367029,RMVar_hsa_circ_286770,RMVar_hsa_circ_275346,RMVar_hsa_circ_163756,RMVar_hsa_circ_163758,RMVar_hsa_circ_163757,RMVar_hsa_circ_163755 100131 RMVar_ID_100131 Human_SNP_ID_536550282 m1A Human chr13 - 75335137 75335137 75335137 TAGGAGGCAGCATACTGGCAGAGGGAAGGCCCAGTGCGGGTGTCAGAGCCACAGTGGAGGGGAGC TAGGAGGCAGCATACTGGCAGAGGGAAGGCCCGGTGCGGGTGTCAGAGCCACAGTGGAGGGGAGC T C TBC1D4 Ensembl:ENSG00000136111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75335105..75335245 26863196 MeRIP-seq:(Medium) rs1307784507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24366793 RMVar_hsa_circ_80307,RMVar_hsa_circ_122517,RMVar_hsa_circ_110492,RMVar_hsa_circ_163748,RMVar_hsa_circ_163749,RMVar_hsa_circ_163750,RMVar_hsa_circ_340769,RMVar_hsa_circ_376436,RMVar_hsa_circ_374940,RMVar_hsa_circ_345233,RMVar_hsa_circ_163752,RMVar_hsa_circ_365213,RMVar_hsa_circ_57390,RMVar_hsa_circ_76499,RMVar_hsa_circ_163753,RMVar_hsa_circ_121596,RMVar_hsa_circ_30703,RMVar_hsa_circ_372599,RMVar_hsa_circ_163754,RMVar_hsa_circ_286260,RMVar_hsa_circ_367029,RMVar_hsa_circ_286770,RMVar_hsa_circ_275346,RMVar_hsa_circ_163756,RMVar_hsa_circ_163758,RMVar_hsa_circ_163757,RMVar_hsa_circ_163755 100132 RMVar_ID_100132 Human_SNP_ID_536563717 m1A Human chr13 - 75391905 75391905 75391905 AGTGTGGCCAATGGAGTTGTCACTGGAAAGACAACAGGTGAGTAAAGATCTAAAGAGAGGGACAG AGTGTGGCCAATGGAGTTGTCACTGGAAAGACTACAGGTGAGTAAAGATCTAAAGAGAGGGACAG T A TBC1D4 Ensembl:ENSG00000136111 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75391901..75392059 26863196 MeRIP-seq:(Medium) rs1248390722 Functional Loss SNV dbSNP153 33..33 33 - - - 100133 RMVar_ID_100133 Human_SNP_ID_536584635 m1A Human chr13 + 75481418 75481418 75481418 GCGAGATATGCTGCGCCTTGTGCTCGAAGATGAATACCGCCGGGTTGGGCTGCGTGGCCGACGGA GCGAGATATGCTGCGCCTTGTGCTCGAAGATGGATACCGCCGGGTTGGGCTGCGTGGCCGACGGA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:75481318..75481468 26863410 MeRIP-seq:(Medium) rs755493386 Functional Loss SNV dbSNP153 33..33 33 - - - 100134 RMVar_ID_100134 Human_SNP_ID_536584928 m1A Human chr13 - 75481932 75481932 75481932 GAGCCTCCGAGCCGCGCCCGTGGAAGTGCTGCATGGGGCAGGGCTGCTGAAGCGCGGAGTTCGGG GAGCCTCCGAGCCGCGCCCGTGGAAGTGCTGCGTGGGGCAGGGCTGCTGAAGCGCGGAGTTCGGG T C TBC1D4 Ensembl:ENSG00000136111 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75481881..75482147 26863196 MeRIP-seq:(Medium) rs1190078956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276841 100135 RMVar_ID_100135 Human_SNP_ID_536598299 m1A Human chr13 + 75537566 75537566 75537566 GGGACGGCTGAAGGTCACCGGCTCGCGGACACAGGACTAGGGGAGACCTGGGGAAGGCTCAGGGT GGGACGGCTGAAGGTCACCGGCTCGCGGACACGGGACTAGGGGAGACCTGGGGAAGGCTCAGGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75537520..75537655 26863196 MeRIP-seq:(Medium) rs9543964 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13156,GWAS_ID_13157 100136 RMVar_ID_100136 Human_SNP_ID_536598379 m1A Human chr13 - 75537753 75537753 75537753 GCCGCTGGATGCTAAGTCCGATGTGAGTTCCAACCTGGAAGGAGAGTGGGCAGCGAGGCTCTGGA GCCGCTGGATGCTAAGTCCGATGTGAGTTCCAGCCTGGAAGGAGAGTGGGCAGCGAGGCTCTGGA T C COMMD6 Ensembl:ENSG00000188243 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:75537751..75537825 32194978 MeRIP-seq:(Medium) rs1310124382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879474 Human_Splice_Rec_1471731,Human_Splice_Rec_1471739,Human_Splice_Rec_1471751,Human_Splice_Rec_1471757,Human_Splice_Rec_1471763,Human_Splice_Rec_1471771,Human_Splice_Rec_1471781,Human_Splice_Rec_1471785,Human_Splice_Rec_1471791 100137 RMVar_ID_100137 Human_SNP_ID_536598409 m1A Human chr13 - 75537789 75537789 75537789 GTCCCAGACGCTGCCCATGGAGGCGTCCAGCGAGCCGCCGCTGGATGCTAAGTCCGATGTGAGTT GTCCCAGACGCTGCCCATGGAGGCGTCCAGCGGGCCGCCGCTGGATGCTAAGTCCGATGTGAGTT T C COMMD6 Ensembl:ENSG00000188243 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75537719..75537791 26863196 MeRIP-seq:(Medium) rs1465358799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_438824,Human_RBP_ID_4273842,Human_RBP_ID_17360701,Human_RBP_ID_26918007 Human_Splice_Rec_1471729,Human_Splice_Rec_1471737,Human_Splice_Rec_1471749,Human_Splice_Rec_1471755,Human_Splice_Rec_1471761,Human_Splice_Rec_1471771,Human_Splice_Rec_1471779,Human_Splice_Rec_1471783,Human_Splice_Rec_1471791 100138 RMVar_ID_100138 Human_SNP_ID_536598418 m1A Human chr13 + 75537804 75537804 75537804 TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCATGGGCAGCGTCTGGGACTTGCGGCCCGGACTC TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCCTGGGCAGCGTCTGGGACTTGCGGCCCGGACTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:75537723..75537850 26863196 MeRIP-seq:(Medium) rs188582438 Functional Loss SNV dbSNP153 33..33 33 - - - 100139 RMVar_ID_100139 Human_SNP_ID_536598419 m1A Human chr13 + 75537804 75537804 75537804 TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCATGGGCAGCGTCTGGGACTTGCGGCCCGGACTC TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCGTGGGCAGCGTCTGGGACTTGCGGCCCGGACTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:75537723..75537850 26863196 MeRIP-seq:(Medium) rs188582438 Functional Loss SNV dbSNP153 33..33 33 - - - 100140 RMVar_ID_100140 Human_SNP_ID_536598420 m1A Human chr13 + 75537804 75537804 75537804 TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCATGGGCAGCGTCTGGGACTTGCGGCCCGGACTC TAGCATCCAGCGGCGGCTCGCTGGACGCCTCCTTGGGCAGCGTCTGGGACTTGCGGCCCGGACTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:75537723..75537850 26863196 MeRIP-seq:(Medium) rs188582438 Functional Loss SNV dbSNP153 33..33 33 - - - 100141 RMVar_ID_100141 Human_SNP_ID_536601613 m1A Human chr13 - 75549864 75549864 75549864 CCCACGGCCCAGGGCTGCCCCGAAGCGCGCCCACCTCGGGATTGGCCTCCAGCGGCAGCCAGCGT CCCACGGCCCAGGGCTGCCCCGAAGCGCGCCCCCCTCGGGATTGGCCTCCAGCGGCAGCCAGCGT T G lnc-COMMD6-4 RNACentral:URS00008C001A lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:75549751..75560825 26863410 MeRIP-seq:(Medium) rs756178407 Functional Loss SNV dbSNP153 33..33 33 - - - 100142 RMVar_ID_100142 Human_SNP_ID_536604055 m1A Human chr13 + 75560714 75560714 75560714 TGTATAGTATACTAGTTTTCTTTTACCAACTAATGTTCCATTGTTTTTTTTTTCTTTCTTTCTTT TGTATAGTATACTAGTTTTCTTTTACCAACTAGTGTTCCATTGTTTTTTTTTTCTTTCTTTCTTT A G AL137782.1,UCHL3 Ensembl:ENSG00000261553,Ensembl:ENSG00000118939 lincRNA,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:75560711..75560785 26863196 MeRIP-seq:(Medium) rs769387377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6316500 RMVar_hsa_circ_102695,RMVar_hsa_circ_163767 100143 RMVar_ID_100143 Human_SNP_ID_536621591 m1A Human chr13 + 75635948 75635948 75635948 AGCGGGGGAGGTTTCTTGGCCGGGAAAGGTACAATTGTGTGCAGCTATTTCTGGTATGTCAAGCG AGCGGGGGAGGTTTCTTGGCCGGGAAAGGTACGATTGTGTGCAGCTATTTCTGGTATGTCAAGCG A G AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:75622271..75636074 26863196 MeRIP-seq:(Medium) rs1378630018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9385,RMVar_hsa_circ_348385,RMVar_hsa_circ_279789,RMVar_hsa_circ_285013,RMVar_hsa_circ_305389,RMVar_hsa_circ_7572,RMVar_hsa_circ_163783,RMVar_hsa_circ_126931,RMVar_hsa_circ_163784 100144 RMVar_ID_100144 Human_SNP_ID_536621628 m1A Human chr13 + 75636031 75636031 75636031 CGGGAGGGGCGCCGCTCTCAGGGGCCCGGGAGAGGGCAGGGGCCAGGCGGGCGGGTGCGGGAAGG CGGGAGGGGCGCCGCTCTCAGGGGCCCGGGAGTGGGCAGGGGCCAGGCGGGCGGGTGCGGGAAGG A T AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75635981..75636194 26863196 MeRIP-seq:(Medium) rs1419227853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439508,Human_RBP_ID_8180491 RMVar_hsa_circ_9385,RMVar_hsa_circ_348385,RMVar_hsa_circ_279789,RMVar_hsa_circ_285013,RMVar_hsa_circ_305389,RMVar_hsa_circ_7572,RMVar_hsa_circ_163783,RMVar_hsa_circ_126931,RMVar_hsa_circ_163784 100145 RMVar_ID_100145 Human_SNP_ID_536621684 m1A Human chr13 + 75636204 75636204 75636204 ACAGTCTGACCACAGAGGCGGCCGCGGCCGGGAGCCCGGGGAGCCAAGGGAGGGGCAGACGGAAG ACAGTCTGACCACAGAGGCGGCCGCGGCCGGGGGCCCGGGGAGCCAAGGGAGGGGCAGACGGAAG A G AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75618868..75636219 26863196 MeRIP-seq:(Medium) rs1262621812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9385,RMVar_hsa_circ_348385,RMVar_hsa_circ_279789,RMVar_hsa_circ_285013,RMVar_hsa_circ_305389,RMVar_hsa_circ_7572,RMVar_hsa_circ_163783,RMVar_hsa_circ_126931,RMVar_hsa_circ_163784 100146 RMVar_ID_100146 Human_SNP_ID_536635648 m1A Human chr13 - 75694384 75694384 75694384 CATTCTGCCTGCAGAGTGAGGCCTTCCTACCTACCTTCGAGCCCCTTCGCCCCTTCATTCTCACA CATTCTGCCTGCAGAGTGAGGCCTTCCTACCTCCCTTCGAGCCCCTTCGCCCCTTCATTCTCACA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:75694381..75694475 26863196 MeRIP-seq:(Medium) rs1461403360 Functional Loss SNV dbSNP153 33..33 33 - - - 100147 RMVar_ID_100147 Human_SNP_ID_536658298 m1A Human chr13 + 75779941 75779941 75779941 AGATAAATTTTAAAGCTGGATGTCCGGGGGAGACATCACATGTTGGCAGGTTCCGTGATGCCCCC AGATAAATTTTAAAGCTGGATGTCCGGGGGAGGCATCACATGTTGGCAGGTTCCGTGATGCCCCC A G AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75779937..75780037 26863196 MeRIP-seq:(Medium) rs1181762051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85071,RMVar_hsa_circ_20592,RMVar_hsa_circ_7572,RMVar_hsa_circ_369004,RMVar_hsa_circ_42901,RMVar_hsa_circ_103887,RMVar_hsa_circ_114831,RMVar_hsa_circ_127494,RMVar_hsa_circ_120097,RMVar_hsa_circ_111701,RMVar_hsa_circ_101302,RMVar_hsa_circ_102689,RMVar_hsa_circ_99773,RMVar_hsa_circ_163788,RMVar_hsa_circ_163792,RMVar_hsa_circ_163794,RMVar_hsa_circ_163796,RMVar_hsa_circ_77705,RMVar_hsa_circ_163797,RMVar_hsa_circ_163795,RMVar_hsa_circ_163793,RMVar_hsa_circ_163790,RMVar_hsa_circ_163791,RMVar_hsa_circ_163789,RMVar_hsa_circ_63058,RMVar_hsa_circ_338406,RMVar_hsa_circ_364606,RMVar_hsa_circ_365834,RMVar_hsa_circ_356880,RMVar_hsa_circ_351370,RMVar_hsa_circ_102218,RMVar_hsa_circ_163799,RMVar_hsa_circ_163800 100148 RMVar_ID_100148 Human_SNP_ID_536660723 m1A Human chr13 + 75788958 75788958 75788958 TCATGAGTTGCAGTTGTTCTGGGCAACAAAGCAAGGCGGATACTTATTCTGGTAGCAGGGTGGAG TCATGAGTTGCAGTTGTTCTGGGCAACAAAGCCAGGCGGATACTTATTCTGGTAGCAGGGTGGAG A C AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:75788924..75789009 26863196 MeRIP-seq:(Medium) rs1430440567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5562315 RMVar_hsa_circ_85071,RMVar_hsa_circ_20592,RMVar_hsa_circ_7572,RMVar_hsa_circ_369004,RMVar_hsa_circ_42901,RMVar_hsa_circ_103887,RMVar_hsa_circ_114831,RMVar_hsa_circ_127494,RMVar_hsa_circ_120097,RMVar_hsa_circ_111701,RMVar_hsa_circ_101302,RMVar_hsa_circ_102689,RMVar_hsa_circ_99773,RMVar_hsa_circ_163788,RMVar_hsa_circ_163792,RMVar_hsa_circ_163794,RMVar_hsa_circ_163796,RMVar_hsa_circ_77705,RMVar_hsa_circ_163797,RMVar_hsa_circ_163795,RMVar_hsa_circ_163793,RMVar_hsa_circ_163790,RMVar_hsa_circ_163791,RMVar_hsa_circ_163789,RMVar_hsa_circ_63058,RMVar_hsa_circ_338406,RMVar_hsa_circ_364606,RMVar_hsa_circ_365834,RMVar_hsa_circ_356880,RMVar_hsa_circ_351370,RMVar_hsa_circ_102218,RMVar_hsa_circ_163799,RMVar_hsa_circ_163800 100149 RMVar_ID_100149 Human_SNP_ID_536673331 m1A Human chr13 + 75840461 75840461 75840461 GTGGGATCAAGAGGAGGAGCGGAAGCGGCAGGAGAGGTGGCAGAAGGAGCAGGACCGCCTACTGC GTGGGATCAAGAGGAGGAGCGGAAGCGGCAGGGGAGGTGGCAGAAGGAGCAGGACCGCCTACTGC A G LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75840401..75840500 26863196 MeRIP-seq:(Medium) rs765272942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756068,Human_RBP_ID_812120,Human_RBP_ID_879483,Human_RBP_ID_9367996,Human_RBP_ID_18978905,Human_RBP_ID_24543590 Human_Splice_Rec_1471946,Human_Splice_Rec_1471947,Human_Splice_Rec_1472004,Human_Splice_Rec_1472005,Human_Splice_Rec_1472076,Human_Splice_Rec_1472077,Human_Splice_Rec_1472126,Human_Splice_Rec_1472127,Human_Splice_Rec_1472192,Human_Splice_Rec_1472193,Human_Splice_Rec_1472252,Human_Splice_Rec_1472253,Human_Splice_Rec_1472306,Human_Splice_Rec_1472307,Human_Splice_Rec_1472376,Human_Splice_Rec_1472377,Human_Splice_Rec_1472410,Human_Splice_Rec_1472411,Human_Splice_Rec_1472432,Human_Splice_Rec_1472433,Human_Splice_Rec_1472440,Human_Splice_Rec_1472441 RMVar_hsa_circ_103887,RMVar_hsa_circ_114831,RMVar_hsa_circ_102689,RMVar_hsa_circ_99773,RMVar_hsa_circ_163788,RMVar_hsa_circ_163790,RMVar_hsa_circ_163791,RMVar_hsa_circ_163789,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_22073,RMVar_hsa_circ_26695,RMVar_hsa_circ_70960,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372 100150 RMVar_ID_100150 Human_SNP_ID_536676595 m1A Human chr13 + 75853252 75853252 75853252 TGGTGTCCACATCAAACCGTGCCTACATGCGGAACCCCTCCTCCAGCGTGCCCCCACCTTCAGCT TGGTGTCCACATCAAACCGTGCCTACATGCGGGACCCCTCCTCCAGCGTGCCCCCACCTTCAGCT A G LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:75853201..75853326 26863196 MeRIP-seq:(Medium) rs1395255465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17245972 Human_miRNA_ID_2153491,Human_miRNA_ID_2801370,Human_miRNA_ID_3009501 RMVar_hsa_circ_114831,RMVar_hsa_circ_163788,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372,RMVar_hsa_circ_29053,RMVar_hsa_circ_38367 100151 RMVar_ID_100151 Human_SNP_ID_536676607 m1A Human chr13 + 75853275 75853275 75853275 TACATGCGGAACCCCTCCTCCAGCGTGCCCCCACCTTCAGCTGGCTCCGTGAAGACCTCCACCAC TACATGCGGAACCCCTCCTCCAGCGTGCCCCCGCCTTCAGCTGGCTCCGTGAAGACCTCCACCAC A G LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75853226..75853336 26863196 MeRIP-seq:(Medium) rs1193678845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17245972 RMVar_hsa_circ_114831,RMVar_hsa_circ_163788,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372,RMVar_hsa_circ_29053,RMVar_hsa_circ_38367 100152 RMVar_ID_100152 Human_SNP_ID_536676629 m1A Human chr13 + 75853325 75853325 75853325 GAAGACCTCCACCACAGGTGTGGCCACCACACAGTCCCCCACCCCGAGAAGCCATTCCCCTTCAG GAAGACCTCCACCACAGGTGTGGCCACCACACTGTCCCCCACCCCGAGAAGCCATTCCCCTTCAG A T LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr13:75853176..75853350;chr13:75853182..75853340 26863196 MeRIP-seq:(Medium) rs1383790615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17245972 Human_Splice_Rec_1471959,Human_Splice_Rec_1472017,Human_Splice_Rec_1472139,Human_Splice_Rec_1472205,Human_Splice_Rec_1472265,Human_Splice_Rec_1472319,Human_Splice_Rec_1472445 Human_miRNA_ID_2076218 RMVar_hsa_circ_114831,RMVar_hsa_circ_163788,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372,RMVar_hsa_circ_29053,RMVar_hsa_circ_38367 100153 RMVar_ID_100153 Human_SNP_ID_536676634 m1A Human chr13 + 75853333 75853333 75853333 CCACCACAGGTGTGGCCACCACACAGTCCCCCACCCCGAGAAGCCATTCCCCTTCAGCTTCACAG CCACCACAGGTGTGGCCACCACACAGTCCCCCCCCCCGAGAAGCCATTCCCCTTCAGCTTCACAG A C LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:75853203..75853400 26863196 MeRIP-seq:(Medium) rs754898427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9367618,Human_RBP_ID_17245972 Human_Splice_Rec_1471959,Human_Splice_Rec_1472017,Human_Splice_Rec_1472139,Human_Splice_Rec_1472205,Human_Splice_Rec_1472265,Human_Splice_Rec_1472319,Human_Splice_Rec_1472445 RMVar_hsa_circ_114831,RMVar_hsa_circ_163788,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372,RMVar_hsa_circ_29053,RMVar_hsa_circ_38367 100154 RMVar_ID_100154 Human_SNP_ID_536939550 m1A Human chr13 - 76884924 76884923 76884924 GAACCGAGAGAACCCAGAGGAACCCCCACCCCACCCCCACCTACCACTCCATGCTTTCTCTACTC GAACCGAGAGAACCCAGAGGAACCCCCACCCC_CCCCCACCTACCACTCCATGCTTTCTCTACTC GT G KCTD12 Ensembl:ENSG00000178695 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1428328514 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_230729,Human_RBP_ID_439131,Human_RBP_ID_22181864,Human_RBP_ID_26426970,Human_RBP_ID_27222560 100155 RMVar_ID_100155 Human_SNP_ID_536939551 m1A Human chr13 - 76884924 76884924 76884924 GAACCGAGAGAACCCAGAGGAACCCCCACCCCACCCCCACCTACCACTCCATGCTTTCTCTACTC GAACCGAGAGAACCCAGAGGAACCCCCACCCCCCCCCCACCTACCACTCCATGCTTTCTCTACTC T G KCTD12 Ensembl:ENSG00000178695 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs953550553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230729,Human_RBP_ID_439131,Human_RBP_ID_22181864,Human_RBP_ID_26426970,Human_RBP_ID_27222560 100156 RMVar_ID_100156 Human_SNP_ID_536939825 m1A Human chr13 - 76885563 76885563 76885563 GTCCGTCCGGGGGCGCGGCGGGCCCGCTGCTCACGCCGTCCCAGTCGCTGGACGGCAGCCGGCGC GTCCGTCCGGGGGCGCGGCGGGCCCGCTGCTCCCGCCGTCCCAGTCGCTGGACGGCAGCCGGCGC T G KCTD12 Ensembl:ENSG00000178695 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:76885462..76885743 26863410 MeRIP-seq:(Medium) rs1183823276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4274065 100157 RMVar_ID_100157 Human_SNP_ID_536940180 m1A Human chr13 - 76886216 76886216 76886216 TGAGCGAGCGTCCGGGTTCCGGGGCTCCGGGGAAGGCGGTTGCAGCTCCTGAGTGCAGCGCGGCT TGAGCGAGCGTCCGGGTTCCGGGGCTCCGGGGCAGGCGGTTGCAGCTCCTGAGTGCAGCGCGGCT T G KCTD12 Ensembl:ENSG00000178695 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:76885941..76886510 26863410 MeRIP-seq:(Medium) rs1422720105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4279767,Human_RBP_ID_8248936,Human_RBP_ID_26918147 100158 RMVar_ID_100158 Human_SNP_ID_536940216 m1A Human chr13 + 76886279 76886264 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCG_______________CCGCCGCCACCGCCACCGCCGCCACCTCCTAG GCCGCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1263982180 Functional Loss DEL dbSNP153 19..33 33 - - - 100159 RMVar_ID_100159 Human_SNP_ID_536940221 m1A Human chr13 + 76886279 76886267 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCGCCG____________CCGCCGCCACCGCCACCGCCGCCACCTCCTAG GCCGCCGCCGCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1021745172 Functional Loss DEL dbSNP153 22..33 33 - - - 100160 RMVar_ID_100160 Human_SNP_ID_536940238 m1A Human chr13 + 76886279 76886273 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCGCCGCCGCCG______CCGCCGCCACCGCCACCGCCGCCACCTCCTAG GCCGCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1555308957 Functional Loss DEL dbSNP153 28..33 33 - - - 100161 RMVar_ID_100161 Human_SNP_ID_536940241 m1A Human chr13 + 76886279 76886276 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCGCCGCCGCCGCCG___CCGCCGCCACCGCCACCGCCGCCACCTCCTAG GCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1186168174 Functional Loss DEL dbSNP153 31..33 33 - - - 100162 RMVar_ID_100162 Human_SNP_ID_536940243 m1A Human chr13 + 76886279 76886279 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCGCCACCTCCTAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs973803018 Functional Loss SNV dbSNP153 33..33 33 - - - 100163 RMVar_ID_100163 Human_SNP_ID_536940290 m1A Human chr13 + 76886303 76886303 76886303 CCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCG CCGCCGCCACCGCCGCCACCGCCACCGCCGCCGCCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:76885991..76886340 26863196 MeRIP-seq:(Medium) rs1220669530 Functional Loss SNV dbSNP153 33..33 33 - - - 100164 RMVar_ID_100164 Human_SNP_ID_536940307 m1A Human chr13 + 76886336 76886336 76886336 CCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCGAGCGCGCCGCTGTGCGCCCCCTTGAGTTCCAGT CCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCGGGCGCGCCGCTGTGCGCCCCCTTGAGTTCCAGT A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:76886240..76886340 26863410 MeRIP-seq:(Medium) rs1401810142 Functional Loss SNV dbSNP153 33..33 33 - - - 100165 RMVar_ID_100165 Human_SNP_ID_536940308 m1A Human chr13 + 76886336 76886336 76886336 CCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCGAGCGCGCCGCTGTGCGCCCCCTTGAGTTCCAGT CCTCCTAGAGCCGCGCGGAGCCGAGCGGTGCGTGCGCGCCGCTGTGCGCCCCCTTGAGTTCCAGT A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:76886240..76886340 26863410 MeRIP-seq:(Medium) rs1401810142 Functional Loss SNV dbSNP153 33..33 33 - - - 100166 RMVar_ID_100166 Human_SNP_ID_536965279 m1A Human chr13 - 76992219 76992219 76992219 GCGCCGGGAGGGGATGCCCGAGACCCGGGACCAGCCCGGAACCACCGCGAGCCAAAGCAGCGCCA GCGCCGGGAGGGGATGCCCGAGACCCGGGACCGGCCCGGAACCACCGCGAGCCAAAGCAGCGCCA T C lnc-FBXL3-1,lnc-FBXL3-1:2 RNACentral:URS00008B51BF,RNACentral:URS00008BA5BC lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:76992131..76992262 26863196 MeRIP-seq:(Medium) rs1332500298 Functional Loss SNV dbSNP153 33..33 33 - - - 100167 RMVar_ID_100167 Human_SNP_ID_536974280 m1A Human chr13 - 77027102 77027102 77027102 CAGGAAGCTTACGCGGTGGCAGCCGCTCGCTGAGGTAGTCTCTCGCGGCGCCGGGGATCCCTGAA CAGGAAGCTTACGCGGTGGCAGCCGCTCGCTGGGGTAGTCTCTCGCGGCGCCGGGGATCCCTGAA T C FBXL3 Ensembl:ENSG00000005812 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:77021830..77027150 26863196 MeRIP-seq:(Medium) rs867566801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276657,Human_RBP_ID_12220483,Human_RBP_ID_22919864,Human_RBP_ID_23604518 RMVar_hsa_circ_113292,RMVar_hsa_circ_163810,RMVar_hsa_circ_163816,RMVar_hsa_circ_81248 100168 RMVar_ID_100168 Human_SNP_ID_536974281 m1A Human chr13 - 77027102 77027102 77027102 CAGGAAGCTTACGCGGTGGCAGCCGCTCGCTGAGGTAGTCTCTCGCGGCGCCGGGGATCCCTGAA CAGGAAGCTTACGCGGTGGCAGCCGCTCGCTGCGGTAGTCTCTCGCGGCGCCGGGGATCCCTGAA T G FBXL3 Ensembl:ENSG00000005812 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:77021830..77027150 26863196 MeRIP-seq:(Medium) rs867566801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276657,Human_RBP_ID_12220483,Human_RBP_ID_22919864,Human_RBP_ID_23604518 RMVar_hsa_circ_113292,RMVar_hsa_circ_163810,RMVar_hsa_circ_163816,RMVar_hsa_circ_81248 100169 RMVar_ID_100169 Human_SNP_ID_536990541 m1A Human chr13 - 77097506 77097506 77097506 AAAAAGGAAAAAAAGAAAAAAGAAAAGGCAGAAGTTAGGCCCAGGGGTAATTTGTTTGGAGAGAT AAAAAGGAAAAAAAGAAAAAAGAAAAGGCAGAGGTTAGGCCCAGGGGTAATTTGTTTGGAGAGAT T C MYCBP2 Ensembl:ENSG00000005810 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:77097455..77097520 26863196 MeRIP-seq:(Medium) rs1359306701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1065636,Human_RBP_ID_4274303,Human_RBP_ID_5463022,Human_RBP_ID_22918301 RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_114583,RMVar_hsa_circ_163819,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_104360,RMVar_hsa_circ_163824,RMVar_hsa_circ_62615,RMVar_hsa_circ_111742,RMVar_hsa_circ_163829,RMVar_hsa_circ_90209,RMVar_hsa_circ_163830,RMVar_hsa_circ_41277,RMVar_hsa_circ_92722,RMVar_hsa_circ_313131,RMVar_hsa_circ_163835,RMVar_hsa_circ_163834,RMVar_hsa_circ_269463,RMVar_hsa_circ_75815,RMVar_hsa_circ_119106,RMVar_hsa_circ_163837,RMVar_hsa_circ_163838,RMVar_hsa_circ_124062,RMVar_hsa_circ_372863,RMVar_hsa_circ_163840,RMVar_hsa_circ_163841,RMVar_hsa_circ_17600,RMVar_hsa_circ_29200,RMVar_hsa_circ_103834,RMVar_hsa_circ_357671,RMVar_hsa_circ_109703,RMVar_hsa_circ_100074,RMVar_hsa_circ_106116,RMVar_hsa_circ_163844,RMVar_hsa_circ_163845,RMVar_hsa_circ_163843,RMVar_hsa_circ_313569,RMVar_hsa_circ_93607,RMVar_hsa_circ_163846,RMVar_hsa_circ_163847,RMVar_hsa_circ_266740 100170 RMVar_ID_100170 Human_SNP_ID_537044577 m1A Human chr13 - 77326697 77326697 77326697 GGCTCGGCGGGGACGGATTCTACCCAGCCGCCACCTTCTCTTCCTCCCCGGCGCCGGGGGCGCTG GGCTCGGCGGGGACGGATTCTACCCAGCCGCCTCCTTCTCTTCCTCCCCGGCGCCGGGGGCGCTG T A MYCBP2 Ensembl:ENSG00000005810 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:77326586..77326826 26863196 MeRIP-seq:(Medium) rs973104530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18978607 RMVar_hsa_circ_122811,RMVar_hsa_circ_163821,RMVar_hsa_circ_90181,RMVar_hsa_circ_163935 100171 RMVar_ID_100171 Human_SNP_ID_537356467 m1A Human chr13 + 78602225 78602192 78602225 CCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCACCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC _________________________________CCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC GCCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCA G OBI1-AS1 Ensembl:ENSG00000234377 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:78602158..78602259 26863410 MeRIP-seq:(Medium) rs1173474908 Functional Loss DEL dbSNP153 1..33 33 - - - 100172 RMVar_ID_100172 Human_SNP_ID_537356474 m1A Human chr13 + 78602225 78602195 78602225 CCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCACCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC CCG______________________________CCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC GCCCGGGCCGCCGCCGCCGCCCGGGCCGCCA G OBI1-AS1 Ensembl:ENSG00000234377 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:78602158..78602259 26863410 MeRIP-seq:(Medium) rs1248560585 Functional Loss DEL dbSNP153 4..33 33 - - - 100173 RMVar_ID_100173 Human_SNP_ID_537356502 m1A Human chr13 + 78602225 78602222 78602225 CCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCACCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC CCGCCCGGGCCGCCGCCGCCGCCCGGGCCG___CCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC GCCA G OBI1-AS1 Ensembl:ENSG00000234377 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:78602158..78602259 26863410 MeRIP-seq:(Medium) rs1424803850 Functional Loss DEL dbSNP153 31..33 33 - - - 100174 RMVar_ID_100174 Human_SNP_ID_537356503 m1A Human chr13 + 78602225 78602225 78602225 CCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCACCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC CCGCCCGGGCCGCCGCCGCCGCCCGGGCCGCCGCCGCCCCCCGGGCCGTCGTGGGCGCCGCCGCC A G OBI1-AS1 Ensembl:ENSG00000234377 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:78602158..78602259 26863410 MeRIP-seq:(Medium) rs1192879491 Functional Loss SNV dbSNP153 33..33 33 - - - 100175 RMVar_ID_100175 Human_SNP_ID_537359947 m1A Human chr13 - 78614399 78614399 78614399 TGGTATGCCTATATAGGTCTTTAAAAATGGGTATGTATGCTGTTTAATGTGCACTGAACATTTTA TGGTATGCCTATATAGGTCTTTAAAAATGGGTTTGTATGCTGTTTAATGTGCACTGAACATTTTA T A OBI1 Ensembl:ENSG00000152193 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_439515,Human_RBP_ID_1486149,Human_RBP_ID_1812478,Human_RBP_ID_8946812,Human_RBP_ID_12226381,Human_RBP_ID_23605325 Human_miRNA_ID_1072167,Human_miRNA_ID_1258550,Human_miRNA_ID_2986913 GWAS_ID_13158,GWAS_ID_13159,GWAS_ID_13160,GWAS_ID_13161,GWAS_ID_13162,GWAS_ID_13163,GWAS_ID_13164,GWAS_ID_13165,GWAS_ID_13166,GWAS_ID_13167,GWAS_ID_13168,GWAS_ID_13169,GWAS_ID_13170,GWAS_ID_13171,GWAS_ID_13172,GWAS_ID_13173,GWAS_ID_13174,GWAS_ID_13175,GWAS_ID_13176,GWAS_ID_13177,GWAS_ID_13178,GWAS_ID_13179,GWAS_ID_13180,GWAS_ID_13181,GWAS_ID_13182 RMVar_hsa_circ_163958,RMVar_hsa_circ_93754 100176 RMVar_ID_100176 Human_SNP_ID_537371158 m1A Human chr13 + 78658978 78658974 78658979 CGCGCCTCACGCCCCTTCCCCGCCCCCGCACGAGACGGCCCTCGGCCCCGGCGAGCGACTTATCC CGCGCCTCACGCCCCTTCCCCGCCCCCGC_____ACGGCCCTCGGCCCCGGCGAGCGACTTATCC CACGAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:78658853..78658984 26863196 MeRIP-seq:(Medium) rs368698200 Functional Loss DEL dbSNP153 30..34 33 - - - 100177 RMVar_ID_100177 Human_SNP_ID_537371240 m1A Human chr13 - 78659111 78659111 78659111 TTGGCGGGATTCTGAACGCTGCCATGGCTCAGACCGTGCAGAATGTTACATTGTCGCTCACTCTG TTGGCGGGATTCTGAACGCTGCCATGGCTCAGTCCGTGCAGAATGTTACATTGTCGCTCACTCTG T A OBI1 Ensembl:ENSG00000152193 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:78659000..78659116 26863196 MeRIP-seq:(Medium) rs1451013646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1486184,Human_RBP_ID_4276658,Human_RBP_ID_22182270,Human_RBP_ID_22796563,Human_RBP_ID_23605470 Human_Splice_Rec_1473783 Human_miRNA_ID_1163325,Human_miRNA_ID_1217344 100178 RMVar_ID_100178 Human_SNP_ID_537538827 m1A Human chr13 - 79337249 79337249 79337249 TCATCTGGTCGGGGCAGAGGAATTCATTCAAGAGGTCGAGGTGCAGTTCATGGCCGAGGCAGGGG TCATCTGGTCGGGGCAGAGGAATTCATTCAAGGGGTCGAGGTGCAGTTCATGGCCGAGGCAGGGG T C RBM26 Ensembl:ENSG00000139746 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:79337101..79337353 26863196 MeRIP-seq:(Medium) rs749845479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4274722,Human_RBP_ID_6306225,Human_RBP_ID_8791494,Human_RBP_ID_12228764,Human_RBP_ID_17842209,Human_RBP_ID_18435400,Human_RBP_ID_22796968,Human_RBP_ID_26324142,Human_RBP_ID_26918806,Human_RBP_ID_27807993 Human_Splice_Rec_1473874,Human_Splice_Rec_1473914,Human_Splice_Rec_1473956,Human_Splice_Rec_1473996,Human_Splice_Rec_1474038 Human_miRNA_ID_2750845 RMVar_hsa_circ_54280,RMVar_hsa_circ_359752,RMVar_hsa_circ_361603,RMVar_hsa_circ_358642,RMVar_hsa_circ_41167,RMVar_hsa_circ_163966,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_361123,RMVar_hsa_circ_370435,RMVar_hsa_circ_21627,RMVar_hsa_circ_325909,RMVar_hsa_circ_163967,RMVar_hsa_circ_267650,RMVar_hsa_circ_163965,RMVar_hsa_circ_377260 100179 RMVar_ID_100179 Human_SNP_ID_537538843 m1A Human chr13 + 79337300 79337300 79337300 CCCCGACCAGATGAAAGAATCCCTCGTTTGGCAGCCTAGAAGAGATTAGACACACAGGTTAAACA CCCCGACCAGATGAAAGAATCCCTCGTTTGGCCGCCTAGAAGAGATTAGACACACAGGTTAAACA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:79337126..79337350 26863196 MeRIP-seq:(Medium) rs150357035 Functional Loss SNV dbSNP153 33..33 33 - - - 100180 RMVar_ID_100180 Human_SNP_ID_537539723 m1A Human chr13 - 79341076 79341076 79341076 AACTACACAGTAGGCTTAAAAGAAGCAAATGTAGTTGTAGTGGTCAATTTAAAAATATATTCCCT AACTACACAGTAGGCTTAAAAGAAGCAAATGTCGTTGTAGTGGTCAATTTAAAAATATATTCCCT T G RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:79341074..79341250 26863196 MeRIP-seq:(Medium) rs367921168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_439711,Human_RBP_ID_1486276,Human_RBP_ID_8395711 RMVar_hsa_circ_54280,RMVar_hsa_circ_359752,RMVar_hsa_circ_361603,RMVar_hsa_circ_358642,RMVar_hsa_circ_163966,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_370435,RMVar_hsa_circ_21627,RMVar_hsa_circ_325909,RMVar_hsa_circ_163967,RMVar_hsa_circ_267650,RMVar_hsa_circ_163965,RMVar_hsa_circ_377260 100181 RMVar_ID_100181 Human_SNP_ID_537556897 m1A Human chr13 + 79403751 79403751 79403751 AGACATTCTGCTCCAGAGTTCTCCTCACCGCTATACTATGATGCCCACTCTCCAATACACCGAAA AGACATTCTGCTCCAGAGTTCTCCTCACCGCTCTACTATGATGCCCACTCTCCAATACACCGAAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:79403749..79404261 26863196 MeRIP-seq:(Medium) rs976060298 Functional Loss SNV dbSNP153 33..33 33 - - - 100182 RMVar_ID_100182 Human_SNP_ID_537557098 m1A Human chr13 - 79404577 79404577 79404577 TTTCAGGAAGAGAAAGGCCACTGTGGCTGGAAAGAGCCTTGTGATGAGGGAGAGGATATAAAGGC TTTCAGGAAGAGAAAGGCCACTGTGGCTGGAAGGAGCCTTGTGATGAGGGAGAGGATATAAAGGC T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:79404534..79404627 26863196 MeRIP-seq:(Medium) rs1566624482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_439732,Human_RBP_ID_9745663,Human_RBP_ID_12231789,Human_RBP_ID_23606025 100183 RMVar_ID_100183 Human_SNP_ID_537557497 m1A Human chr13 - 79405884 79405884 79405884 GGGCCCGCGGGAACCTGCCACCGGCGCCTCCCACCGCGGCCCACGCGGGCGGCGCGCGGAGGAGG GGGCCCGCGGGAACCTGCCACCGGCGCCTCCCCCCGCGGCCCACGCGGGCGGCGCGCGGAGGAGG T G RBM26 Ensembl:ENSG00000139746 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:79405792..79405982 26863410 MeRIP-seq:(Medium) rs1459159220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230674,Human_RBP_ID_4276475,Human_RBP_ID_5351121,Human_RBP_ID_5522399,Human_RBP_ID_22438203 100184 RMVar_ID_100184 Human_SNP_ID_537575445 m1A Human chr13 + 79481361 79481361 79481361 AGCCACAGGAAGTGAAGAGCTTCCGCCGGGAGACCGCGGCTGCAGGAACGGAGGCGGAAGGGGCC AGCCACAGGAAGTGAAGAGCTTCCGCCGGGAGGCCGCGGCTGCAGGAACGGAGGCGGAAGGGGCC A G NDFIP2 Ensembl:ENSG00000102471 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:79481311..79481457 26863196 MeRIP-seq:(Medium) rs1243147302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755924,Human_RBP_ID_4276659,Human_RBP_ID_6307037,Human_RBP_ID_27807758 RMVar_hsa_circ_127401,RMVar_hsa_circ_163985 100185 RMVar_ID_100185 Human_SNP_ID_537575452 m1A Human chr13 - 79481369 79481369 79481369 CGCCGCAGGGCCCCTTCCGCCTCCGTTCCTGCAGCCGCGGTCTCCCGGCGGAAGCTCTTCACTTC CGCCGCAGGGCCCCTTCCGCCTCCGTTCCTGCCGCCGCGGTCTCCCGGCGGAAGCTCTTCACTTC T G NDFIP2-AS1 RNACentral:URS00009BA752 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:79481319..79481473 26863196 MeRIP-seq:(Medium) rs1201098970 Functional Loss SNV dbSNP153 33..33 33 - - - 100186 RMVar_ID_100186 Human_SNP_ID_537778361 m1A Human chr13 + 80337050 80337050 80337050 AACAGTGATAGAAGAGACCTTTCACACAGCATACACAAGTCCCATAGTCAATCACGTTCTGGGCC AACAGTGATAGAAGAGACCTTTCACACAGCATGCACAAGTCCCATAGTCAATCACGTTCTGGGCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:80336971..80337071 32194978 MeRIP-seq:(Medium) rs766828965 Functional Loss SNV dbSNP153 33..33 33 - - - 100187 RMVar_ID_100187 Human_SNP_ID_537778596 m1A Human chr13 - 80337657 80337657 80337657 AGAGTGGCAACGGGTCGCAGCCCTTGCTGCAGACGCCCCGTGACGGTGGCAGACAGCGTGGGGAG AGAGTGGCAACGGGTCGCAGCCCTTGCTGCAGTCGCCCCGTGACGGTGGCAGACAGCGTGGGGAG T A SPRY2 Ensembl:ENSG00000136158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:80337618..80338744 32194978 MeRIP-seq:(Medium) rs774765586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1474386,Human_Splice_Rec_1474388 100188 RMVar_ID_100188 Human_SNP_ID_539635104 m1A Human chr13 + 87671720 87671720 87671720 TTGTGCGCCGCATCTGGGGAAGGGATACAGAAAAAAACCCTGCAAACACCGTGAGGATGAAACTG TTGTGCGCCGCATCTGGGGAAGGGATACAGAAGAAAACCCTGCAAACACCGTGAGGATGAAACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:87671669..87671768 26863196 MeRIP-seq:(Medium) rs1021421449 Functional Loss SNV dbSNP153 33..33 33 - - - 100189 RMVar_ID_100189 Human_SNP_ID_539637312 m1A Human chr13 + 87677565 87677565 87677565 CGTGTACGGCGGCGGCGGCGGCACGGGCGGCCACCCACACGCGCACGTGCATCACCGCGGGCCCG CGTGTACGGCGGCGGCGGCGGCACGGGCGGCCGCCCACACGCGCACGTGCATCACCGCGGGCCCG A G SLITRK5 Ensembl:ENSG00000165300 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:87677514..87677616 26863196 MeRIP-seq:(Medium) rs760992382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230715 100190 RMVar_ID_100190 Human_SNP_ID_539646031 m1A Human chr13 - 87710154 87710144 87710154 AGGAAGGGAAAGGAGGGAGAAAGTAAGCAGGCAAGAAAGAAAGAGAAAGAAAAGAGAGAGAAAGA AGGAAGGGAAAGGAGGGAGAAAGTAAGCAGGC__________GAGAAAGAAAAGAGAGAGAAAGA CTTTCTTTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:87710118..87710220 26863196 MeRIP-seq:(Medium) rs1297763630 Functional Loss DEL dbSNP153 33..42 33 - - - 100191 RMVar_ID_100191 Human_SNP_ID_653497766 m1A Human chr18 - 75064208 75064208 75064208 TGTCAGGATGTAGTGCGTGGTGCCCTCGGAGAAGCCGCCACTGGACTCCTGCACCATGGCCTGGA TGTCAGGATGTAGTGCGTGGTGCCCTCGGAGAGGCCGCCACTGGACTCCTGCACCATGGCCTGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:75064157..75064723 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 100192 RMVar_ID_100192 Human_SNP_ID_653536177 m1A Human chr18 + 75209045 75209035 75209045 ACATGTCCACGATGGCCCGGGCCCCGGTGGGCACCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC ACATGTCCACGATGGCCCGGGCC__________CCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC CCCGGTGGGCA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:75208862..75209108 26863410 MeRIP-seq:(Medium) rs865829187 Functional Loss DEL dbSNP153 24..33 33 - - - 100193 RMVar_ID_100193 Human_SNP_ID_653536178 m1A Human chr18 + 75209045 75209036 75209045 ACATGTCCACGATGGCCCGGGCCCCGGTGGGCACCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC ACATGTCCACGATGGCCCGGGCCC_________CCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC CCGGTGGGCA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:75208862..75209108 26863410 MeRIP-seq:(Medium) rs1555724186 Functional Loss DEL dbSNP153 25..33 33 - - - 100194 RMVar_ID_100194 Human_SNP_ID_653536179 m1A Human chr18 + 75209045 75209037 75209045 ACATGTCCACGATGGCCCGGGCCCCGGTGGGCACCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC ACATGTCCACGATGGCCCGGGCCCC________CCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC CGGTGGGCA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:75208862..75209108 26863410 MeRIP-seq:(Medium) rs1555724188 Functional Loss DEL dbSNP153 26..33 33 - - - 100195 RMVar_ID_100195 Human_SNP_ID_653536186 m1A Human chr18 + 75209045 75209045 75209045 ACATGTCCACGATGGCCCGGGCCCCGGTGGGCACCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC ACATGTCCACGATGGCCCGGGCCCCGGTGGGCCCCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:75208862..75209108 26863410 MeRIP-seq:(Medium) rs200768449 Functional Loss SNV dbSNP153 33..33 33 - - - 100196 RMVar_ID_100196 Human_SNP_ID_653536278 m1A Human chr18 - 75209225 75209225 75209225 GGGGGCTGCGCCGGCGCCGGGGAGGCGGGGGGAGCGGGAGCGGGCGACGCGGGGAAGGGGGGAGC GGGGGCTGCGCCGGCGCCGGGGAGGCGGGGGGGGCGGGAGCGGGCGACGCGGGGAAGGGGGGAGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:75209148..75209249 26863410 MeRIP-seq:(Medium) rs902122845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5189538,Human_RBP_ID_26783276 100197 RMVar_ID_100197 Human_SNP_ID_653537168 m1A Human chr18 - 75211860 75211839 75211860 GCTTCCTCCTCGGCATGCTGCTCGGCCGCCGCAGCCGTCGCCTCAGCCGCCGCCGGAGTTCGCGG GCTTCCTCCTCGGCATGCTGCTCGGCCGCCGC_____________________CGGAGTTCGCGG GGCGGCGGCTGAGGCGACGGCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:75211817..75211945 26863196 MeRIP-seq:(Medium) rs1220080470 Functional Loss DEL dbSNP153 33..53 33 - - - 100198 RMVar_ID_100198 Human_SNP_ID_653537183 m1A Human chr18 + 75211871 75211871 75211871 GGCGGCGGCTGAGGCGACGGCTGCGGCGGCCGAGCAGCATGCCGAGGAGGAAGCAGCAGGCCCCC GGCGGCGGCTGAGGCGACGGCTGCGGCGGCCGCGCAGCATGCCGAGGAGGAAGCAGCAGGCCCCC A C TSHZ1 Ensembl:ENSG00000179981 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:75211755..75211970 26863196 MeRIP-seq:(Medium) rs1394029736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1925763 100199 RMVar_ID_100199 Human_SNP_ID_653554200 m1A Human chr18 + 75281065 75281065 75281065 GCTGGGCACAGGCGGGGCAGCGGTGAGGGTCCAGACGCCCTGCCTGGGACACGCAGCTTCAGCAA GCTGGGCACAGGCGGGGCAGCGGTGAGGGTCCGGACGCCCTGCCTGGGACACGCAGCTTCAGCAA A G TSHZ1 Ensembl:ENSG00000179981 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:75281064..75281270 26863196 MeRIP-seq:(Medium) rs1350429186 Functional Loss SNV dbSNP153 33..33 33 - - - 100200 RMVar_ID_100200 Human_SNP_ID_653555382 m1A Human chr18 + 75285549 75285548 75285549 CTTTGGACATTCAGGAAAGTGAGTACATGTGCAATGAAGAGACGGAGATCAAAGAGGCGCAGAGC CTTTGGACATTCAGGAAAGTGAGTACATGTGC_ATGAAGAGACGGAGATCAAAGAGGCGCAGAGC CA C TSHZ1 Ensembl:ENSG00000179981 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:75285427..75285560 26863196 MeRIP-seq:(Medium) rs1207780018 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1878344,Human_RBP_ID_6705377 Human_miRNA_ID_2275699,Human_miRNA_ID_2401593,Human_miRNA_ID_2495519,Human_miRNA_ID_2501441,Human_miRNA_ID_3109470,Human_miRNA_ID_3110917 RMVar_hsa_circ_190693,RMVar_hsa_circ_377837 100201 RMVar_ID_100201 Human_SNP_ID_653555569 m1A Human chr18 - 75285948 75285930 75285948 GGTACTGGTGGTACTGCTGTGGCTGGTGCTGGAGCTGCAGCTGGTGCTGGGCGTGCTCGTGGTGG GGTACTGGTGGTACTGCTGTGGCTGGTGCTGG__________________GCGTGCTCGTGGTGG CCCAGCACCAGCTGCAGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:75285790..75285972 26863196 MeRIP-seq:(Medium) rs1272368366 Functional Loss DEL dbSNP153 33..50 33 - - - 100202 RMVar_ID_100202 Human_SNP_ID_653555971 m1A Human chr18 + 75286909 75286909 75286909 CGCGGGGTCCACGACTTCTGAAGAAAAGAAAGAGCCAGAGAAGGAGAAGCCGCCTGTGGCTGGCG CGCGGGGTCCACGACTTCTGAAGAAAAGAAAGGGCCAGAGAAGGAGAAGCCGCCTGTGGCTGGCG A G TSHZ1 Ensembl:ENSG00000179981 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:75286860..75286980 26863196 MeRIP-seq:(Medium) rs1484204945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190693,RMVar_hsa_circ_377837 100203 RMVar_ID_100203 Human_SNP_ID_653870703 m1A Human chr18 - 76491219 76491219 76491219 ACTGGGGTCTGCGCGGGGCTCCGGGCCGGGGCAGGCGGGGGTCCGCGCGGCGGCGTGGACCGGGC ACTGGGGTCTGCGCGGGGCTCCGGGCCGGGGCGGGCGGGGGTCCGCGCGGCGGCGTGGACCGGGC T C ZNF516 Ensembl:ENSG00000101493 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:76491134..76491382 26863196 MeRIP-seq:(Medium) rs1467202924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561297,Human_RBP_ID_8194171,Human_RBP_ID_8727803,Human_RBP_ID_9424767,Human_RBP_ID_18420750,Human_RBP_ID_18460791,Human_RBP_ID_18944144,Human_RBP_ID_22718036,Human_RBP_ID_26783179 100204 RMVar_ID_100204 Human_SNP_ID_653870704 m1A Human chr18 - 76491219 76491219 76491219 ACTGGGGTCTGCGCGGGGCTCCGGGCCGGGGCAGGCGGGGGTCCGCGCGGCGGCGTGGACCGGGC ACTGGGGTCTGCGCGGGGCTCCGGGCCGGGGCCGGCGGGGGTCCGCGCGGCGGCGTGGACCGGGC T G ZNF516 Ensembl:ENSG00000101493 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:76491134..76491382 26863196 MeRIP-seq:(Medium) rs1467202924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561297,Human_RBP_ID_8194171,Human_RBP_ID_8727803,Human_RBP_ID_9424767,Human_RBP_ID_18420750,Human_RBP_ID_18460791,Human_RBP_ID_18944144,Human_RBP_ID_22718036,Human_RBP_ID_26783179 100205 RMVar_ID_100205 Human_SNP_ID_653872513 m1A Human chr18 - 76496140 76496140 76496140 CCCGCCCCCGCGCGCCCGCCCTCCCCTCCCCCACCCCGGCCATCCCTGCCCTGTAACAGGAGAGC CCCGCCCCCGCGCGCCCGCCCTCCCCTCCCCCCCCCCGGCCATCCCTGCCCTGTAACAGGAGAGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:76496056..76496183 26863196 MeRIP-seq:(Medium) rs1189796050 Functional Loss SNV dbSNP153 33..33 33 - - - 100206 RMVar_ID_100206 Human_SNP_ID_653964281 m1A Human chr18 + 76822915 76822915 76822915 ACTTTCCTGGGCCGGGCGGCGGCTGAGGCGGGAGGCGGGAGGCGGGTGAGGGAGCAGGCGGCCGC ACTTTCCTGGGCCGGGCGGCGGCTGAGGCGGGCGGCGGGAGGCGGGTGAGGGAGCAGGCGGCCGC A C ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:76822913..76823030 26863196 MeRIP-seq:(Medium) rs939996987 Functional Loss SNV dbSNP153 33..33 33 - - - 100207 RMVar_ID_100207 Human_SNP_ID_653964282 m1A Human chr18 + 76822915 76822915 76822915 ACTTTCCTGGGCCGGGCGGCGGCTGAGGCGGGAGGCGGGAGGCGGGTGAGGGAGCAGGCGGCCGC ACTTTCCTGGGCCGGGCGGCGGCTGAGGCGGGGGGCGGGAGGCGGGTGAGGGAGCAGGCGGCCGC A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:76822913..76823030 26863196 MeRIP-seq:(Medium) rs939996987 Functional Loss SNV dbSNP153 33..33 33 - - - 100208 RMVar_ID_100208 Human_SNP_ID_653970051 m1A Human chr18 + 76843872 76843872 76843872 GTAATCCCAGCACAGGGAAGAAGGTAGAAGGGAGTTTTAAATAAAAGTAAAGAAGAGGCTGGGTG GTAATCCCAGCACAGGGAAGAAGGTAGAAGGGTGTTTTAAATAAAAGTAAAGAAGAGGCTGGGTG A T ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:76843867..76843949 26863196 MeRIP-seq:(Medium) rs1170687705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 100209 RMVar_ID_100209 Human_SNP_ID_653970165 m1A Human chr18 - 76844273 76844273 76844273 CCAAATTGCTACCGCTTTAGGTCATCTCTACCACCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT CCAAATTGCTACCGCTTTAGGTCATCTCTACCTCCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76844265..76844501 26863196 MeRIP-seq:(Medium) rs960951204 Functional Loss SNV dbSNP153 33..33 33 - - - 100210 RMVar_ID_100210 Human_SNP_ID_653970166 m1A Human chr18 - 76844273 76844273 76844273 CCAAATTGCTACCGCTTTAGGTCATCTCTACCACCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT CCAAATTGCTACCGCTTTAGGTCATCTCTACCCCCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76844265..76844501 26863196 MeRIP-seq:(Medium) rs960951204 Functional Loss SNV dbSNP153 33..33 33 - - - 100211 RMVar_ID_100211 Human_SNP_ID_653973819 m1A Human chr18 - 76858719 76858719 76858719 TCCCCCTTCCTCCTCCACCTGCACCTGCCTCCAGCTGAGCCCTCTCCCCCTTCCTCCTCCACCTG TCCCCCTTCCTCCTCCACCTGCACCTGCCTCCCGCTGAGCCCTCTCCCCCTTCCTCCTCCACCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76858591..76858781 26863196 MeRIP-seq:(Medium) rs1211673564 Functional Loss SNV dbSNP153 33..33 33 - - - 100212 RMVar_ID_100212 Human_SNP_ID_653973927 m1A Human chr18 + 76859301 76859301 76859301 AGGAAGGGGGAGAGGACTCAGGTGGAGGTGGAAGTGGAGCAGCTCCTGGTATGTCTTGCACGTGT AGGAAGGGGGAGAGGACTCAGGTGGAGGTGGAGGTGGAGCAGCTCCTGGTATGTCTTGCACGTGT A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76859181..76859337 26863196 MeRIP-seq:(Medium) rs1335691898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1576,RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700,RMVar_hsa_circ_284111,RMVar_hsa_circ_321626,RMVar_hsa_circ_190704,RMVar_hsa_circ_96257,RMVar_hsa_circ_109986,RMVar_hsa_circ_88953,RMVar_hsa_circ_190702,RMVar_hsa_circ_190703,RMVar_hsa_circ_354278,RMVar_hsa_circ_367822,RMVar_hsa_circ_376284,RMVar_hsa_circ_331797,RMVar_hsa_circ_294221,RMVar_hsa_circ_301228,RMVar_hsa_circ_301916,RMVar_hsa_circ_300645,RMVar_hsa_circ_293036,RMVar_hsa_circ_286041,RMVar_hsa_circ_96175,RMVar_hsa_circ_277279,RMVar_hsa_circ_279684,RMVar_hsa_circ_103509,RMVar_hsa_circ_26348,RMVar_hsa_circ_10468,RMVar_hsa_circ_54489,RMVar_hsa_circ_190708,RMVar_hsa_circ_190712,RMVar_hsa_circ_190716,RMVar_hsa_circ_190718,RMVar_hsa_circ_190720,RMVar_hsa_circ_190719,RMVar_hsa_circ_190717,RMVar_hsa_circ_190714,RMVar_hsa_circ_190715,RMVar_hsa_circ_190713,RMVar_hsa_circ_190710,RMVar_hsa_circ_190711,RMVar_hsa_circ_190709,RMVar_hsa_circ_190706,RMVar_hsa_circ_190707,RMVar_hsa_circ_190723,RMVar_hsa_circ_324047,RMVar_hsa_circ_77483,RMVar_hsa_circ_10711,RMVar_hsa_circ_19083,RMVar_hsa_circ_44913,RMVar_hsa_circ_11331,RMVar_hsa_circ_190724,RMVar_hsa_circ_6795,RMVar_hsa_circ_190725 100213 RMVar_ID_100213 Human_SNP_ID_653984058 m1A Human chr18 - 76900886 76900886 76900886 ACATCTGAGTGGAACAGTTTTACCCTGAAACCAGTCCTCCCACCCGACCCCCAATCTGTGGAAAA ACATCTGAGTGGAACAGTTTTACCCTGAAACCGGTCCTCCCACCCGACCCCCAATCTGTGGAAAA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:76900872..76901004 26863196 MeRIP-seq:(Medium) rs1388105409 Functional Loss SNV dbSNP153 33..33 33 - - - 100214 RMVar_ID_100214 Human_SNP_ID_654000446 m1A Human chr18 + 76967521 76967521 76967521 TGTGATCTGTGAGATTTGTGATTTGGTGTTGGAGGTGGTGGTGTGATCTGTGAGATTTGTGATTT TGTGATCTGTGAGATTTGTGATTTGGTGTTGGGGGTGGTGGTGTGATCTGTGAGATTTGTGATTT A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76967318..76967569 26863196 MeRIP-seq:(Medium) rs1212423591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822938,Human_RBP_ID_5291856,Human_RBP_ID_5649329,Human_RBP_ID_17130086,Human_RBP_ID_23778021 100215 RMVar_ID_100215 Human_SNP_ID_654014442 m1A Human chr18 - 77018462 77018458 77018462 AAATGGACTGATATGTGGATGGATGGATGACGAATGGATGAATTGATGGATGCATGCATGCATGA AAATGGACTGATATGTGGATGGATGGATGACG____GATGAATTGATGGATGCATGCATGCATGA CCATT C MBP Ensembl:ENSG00000197971 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:77018419..77018559 26863196 MeRIP-seq:(Medium) rs1440146341 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_16219,RMVar_hsa_circ_363993 100216 RMVar_ID_100216 Human_SNP_ID_654024863 m1A Human chr18 - 77055503 77055503 77055503 GAAGGAATGGAAGGAAAGGAAGGAAAGAAAGGAAAAAGAAAACTGAGCCCATTTTAAGCGCAGTT GAAGGAATGGAAGGAAAGGAAGGAAAGAAAGGCAAAAGAAAACTGAGCCCATTTTAAGCGCAGTT T G MBP Ensembl:ENSG00000197971 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:77055497..77055574 26863196 MeRIP-seq:(Medium) rs1456459804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16219,RMVar_hsa_circ_363993 100217 RMVar_ID_100217 Human_SNP_ID_654036599 m1A Human chr18 - 77098841 77098841 77098841 CCGTGGATAAAAATGCAGCGCGGAGGAGGAACAAGGAACGGCCCGTTTAAATCTGCCCAGACTCA CCGTGGATAAAAATGCAGCGCGGAGGAGGAACGAGGAACGGCCCGTTTAAATCTGCCCAGACTCA T C MBP Ensembl:ENSG00000197971 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:77098831..77098930 26863196 MeRIP-seq:(Medium) rs1204590011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363993,RMVar_hsa_circ_302532,RMVar_hsa_circ_190746,RMVar_hsa_circ_311349 100218 RMVar_ID_100218 Human_SNP_ID_654041855 m1A Human chr18 + 77118660 77118658 77118661 ACACACACACACTACACACCACACACACACACACACTACATACCACACACACACACCACACACAC ACACACACACACTACACACCACACACACACA___ACTACATACCACACACACACACCACACACAC ACAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:77118657..77118960 26863196 MeRIP-seq:(Medium) rs1202932669 Functional Loss DEL dbSNP153 32..34 33 - - - 100219 RMVar_ID_100219 Human_SNP_ID_654041954 m1A Human chr18 - 77118863 77118853 77118864 GTGTGTGTCTGGTGTGTGTGAAGTGTCTGTGGAGTGTGTGTGTGGTGTGTGTCTGTAGTGTCTGT GTGTGTGTCTGGTGTGTGTGAAGTGTCTGTG___________TGGTGTGTGTCTGTAGTGTCTGT ACACACACACTC A MBP Ensembl:ENSG00000197971 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:77118640..77118981 26863196 MeRIP-seq:(Medium) rs1271256702 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_5291790,Human_RBP_ID_23778069 100220 RMVar_ID_100220 Human_SNP_ID_654041956 m1A Human chr18 - 77118863 77118863 77118863 GTGTGTGTCTGGTGTGTGTGAAGTGTCTGTGGAGTGTGTGTGTGGTGTGTGTCTGTAGTGTCTGT GTGTGTGTCTGGTGTGTGTGAAGTGTCTGTGGGGTGTGTGTGTGGTGTGTGTCTGTAGTGTCTGT T C MBP Ensembl:ENSG00000197971 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:77118640..77118981 26863196 MeRIP-seq:(Medium) rs1368904165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5291790,Human_RBP_ID_23778069 100221 RMVar_ID_100221 Human_SNP_ID_654045593 m1A Human chr18 + 77132682 77132682 77132682 CCCGGGCAGGCTGGTCTCGGCTTCAAGCGCCCACGCGCGGGGTCCCCGGGCAGCCTGCTTCGCCT CCCGGGCAGGCTGGTCTCGGCTTCAAGCGCCCGCGCGCGGGGTCCCCGGGCAGCCTGCTTCGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:77132633..77132746 26863196 MeRIP-seq:(Medium) rs978845482 Functional Loss SNV dbSNP153 33..33 33 - - - 100222 RMVar_ID_100222 Human_SNP_ID_654581592 m1A Human chr18 - 79069439 79069439 79069439 TGCGGTTGGCTGCGGCCGCCGCTGCGCTACGCACCGGGTAAAGCGGGATCTGGTCCGCCATGTTC TGCGGTTGGCTGCGGCCGCCGCTGCGCTACGCTCCGGGTAAAGCGGGATCTGGTCCGCCATGTTC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79069313..79069607 26863196 MeRIP-seq:(Medium) rs889132529 Functional Loss SNV dbSNP153 33..33 33 - - - 100223 RMVar_ID_100223 Human_SNP_ID_654581593 m1A Human chr18 - 79069439 79069439 79069439 TGCGGTTGGCTGCGGCCGCCGCTGCGCTACGCACCGGGTAAAGCGGGATCTGGTCCGCCATGTTC TGCGGTTGGCTGCGGCCGCCGCTGCGCTACGCCCCGGGTAAAGCGGGATCTGGTCCGCCATGTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79069313..79069607 26863196 MeRIP-seq:(Medium) rs889132529 Functional Loss SNV dbSNP153 33..33 33 - - - 100224 RMVar_ID_100224 Human_SNP_ID_654589129 m1A Human chr18 + 79096432 79096432 79096432 ATATTGTCCCTAAATGAAACACACTGTAAAGAAGACTGCTTGGCCTATCTCAGCACTCCATTTTT ATATTGTCCCTAAATGAAACACACTGTAAAGAGGACTGCTTGGCCTATCTCAGCACTCCATTTTT A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79096427..79096501 26863196 MeRIP-seq:(Medium) rs1315738832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1224,RMVar_hsa_circ_28973,RMVar_hsa_circ_190753,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_190752 100225 RMVar_ID_100225 Human_SNP_ID_654594540 m1A Human chr18 + 79117587 79117587 79117587 GGAGGAGGTCATCCAGGAGGGTGTGGGTGGGAAGAAGTAGTTGGAAAGGAGGTCAGAGGGCCTGG GGAGGAGGTCATCCAGGAGGGTGTGGGTGGGAGGAAGTAGTTGGAAAGGAGGTCAGAGGGCCTGG A G ATP9B,AC125437.1 Ensembl:ENSG00000166377,Ensembl:ENSG00000267655 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79117436..79117664 26863196 MeRIP-seq:(Medium) rs1371062677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561837,Human_RBP_ID_8194739 RMVar_hsa_circ_1224,RMVar_hsa_circ_55585,RMVar_hsa_circ_275128,RMVar_hsa_circ_190753,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_377671,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190760,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_296410,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_33147,RMVar_hsa_circ_190762,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566 100226 RMVar_ID_100226 Human_SNP_ID_654596515 m1A Human chr18 + 79125028 79125028 79125028 GATGGGGAATTGGAAAGAGGGCCTGGTGAACAATTGGAATGCACAGAGGAATGGGAAGTTTCGTG GATGGGGAATTGGAAAGAGGGCCTGGTGAACAGTTGGAATGCACAGAGGAATGGGAAGTTTCGTG A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79124989..79125112 26863196 MeRIP-seq:(Medium) rs1259537692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6706473 RMVar_hsa_circ_1224,RMVar_hsa_circ_55585,RMVar_hsa_circ_275128,RMVar_hsa_circ_190753,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_377671,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190760,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_296410,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_33147,RMVar_hsa_circ_190762,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566 100227 RMVar_ID_100227 Human_SNP_ID_654596556 m1A Human chr18 + 79125173 79125173 79125173 GAAAAGGTTTCCGATGGTGCAGAGTGCAGACTAAGGGAGGAGAAGACTTGATGTGCTCAGGGAGA GAAAAGGTTTCCGATGGTGCAGAGTGCAGACTGAGGGAGGAGAAGACTTGATGTGCTCAGGGAGA A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79124775..79125306 26863196 MeRIP-seq:(Medium) rs1231957296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9083464 RMVar_hsa_circ_1224,RMVar_hsa_circ_55585,RMVar_hsa_circ_275128,RMVar_hsa_circ_190753,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_377671,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190760,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_296410,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_33147,RMVar_hsa_circ_190762,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566 100228 RMVar_ID_100228 Human_SNP_ID_654601339 m1A Human chr18 - 79145176 79145176 79145176 AGCTTGCACCTTCAGTCACTCTGCACACCGCCAGCTCCGACATGCAGCCTGCACCTTCAGTCACT AGCTTGCACCTTCAGTCACTCTGCACACCGCCGGCTCCGACATGCAGCCTGCACCTTCAGTCACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79145126..79145321 26863196 MeRIP-seq:(Medium) rs1268933612 Functional Loss SNV dbSNP153 33..33 33 - - - 100229 RMVar_ID_100229 Human_SNP_ID_654601513 m1A Human chr18 + 79145754 79145754 79145754 CTGAAGGTGCAGGCTGCATGTCGGGGGAGCTGACGGTGTGCAGAGTGACTGAAGGTGCAGGCTGC CTGAAGGTGCAGGCTGCATGTCGGGGGAGCTGCCGGTGTGCAGAGTGACTGAAGGTGCAGGCTGC A C ATP9B,AC125437.2 Ensembl:ENSG00000166377,Ensembl:ENSG00000279474 Protein coding,Other intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79145703..79145810 26863196 MeRIP-seq:(Medium) rs374132099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561862,Human_RBP_ID_5291859,Human_RBP_ID_5319559,Human_RBP_ID_5649336,Human_RBP_ID_8194722,Human_RBP_ID_21976920,Human_RBP_ID_22476105 RMVar_hsa_circ_190768,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566,RMVar_hsa_circ_276142,RMVar_hsa_circ_277985,RMVar_hsa_circ_292510,RMVar_hsa_circ_323815,RMVar_hsa_circ_289824,RMVar_hsa_circ_277723,RMVar_hsa_circ_273608,RMVar_hsa_circ_274684,RMVar_hsa_circ_66196,RMVar_hsa_circ_190772,RMVar_hsa_circ_6181,RMVar_hsa_circ_190773,RMVar_hsa_circ_190770,RMVar_hsa_circ_190771,RMVar_hsa_circ_190769,RMVar_hsa_circ_10883,RMVar_hsa_circ_318574,RMVar_hsa_circ_190766,RMVar_hsa_circ_190767,RMVar_hsa_circ_190765,RMVar_hsa_circ_354413,RMVar_hsa_circ_302656,RMVar_hsa_circ_305325,RMVar_hsa_circ_271759,RMVar_hsa_circ_190776,RMVar_hsa_circ_190777,RMVar_hsa_circ_190778 100230 RMVar_ID_100230 Human_SNP_ID_654601514 m1A Human chr18 + 79145754 79145754 79145754 CTGAAGGTGCAGGCTGCATGTCGGGGGAGCTGACGGTGTGCAGAGTGACTGAAGGTGCAGGCTGC CTGAAGGTGCAGGCTGCATGTCGGGGGAGCTGGCGGTGTGCAGAGTGACTGAAGGTGCAGGCTGC A G ATP9B,AC125437.2 Ensembl:ENSG00000166377,Ensembl:ENSG00000279474 Protein coding,Other intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79145703..79145810 26863196 MeRIP-seq:(Medium) rs374132099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3561862,Human_RBP_ID_5291859,Human_RBP_ID_5319559,Human_RBP_ID_5649336,Human_RBP_ID_8194722,Human_RBP_ID_21976920,Human_RBP_ID_22476105 RMVar_hsa_circ_190768,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566,RMVar_hsa_circ_276142,RMVar_hsa_circ_277985,RMVar_hsa_circ_292510,RMVar_hsa_circ_323815,RMVar_hsa_circ_289824,RMVar_hsa_circ_277723,RMVar_hsa_circ_273608,RMVar_hsa_circ_274684,RMVar_hsa_circ_66196,RMVar_hsa_circ_190772,RMVar_hsa_circ_6181,RMVar_hsa_circ_190773,RMVar_hsa_circ_190770,RMVar_hsa_circ_190771,RMVar_hsa_circ_190769,RMVar_hsa_circ_10883,RMVar_hsa_circ_318574,RMVar_hsa_circ_190766,RMVar_hsa_circ_190767,RMVar_hsa_circ_190765,RMVar_hsa_circ_354413,RMVar_hsa_circ_302656,RMVar_hsa_circ_305325,RMVar_hsa_circ_271759,RMVar_hsa_circ_190776,RMVar_hsa_circ_190777,RMVar_hsa_circ_190778 100231 RMVar_ID_100231 Human_SNP_ID_654601698 m1A Human chr18 + 79146446 79146430 79146447 TCGGGGGAGCTGGCGGTGTGGAGAGTGACCGAAGGTGCAGGCTGCATGTCGGGGGAGCTGGCGGT TCGGGGGAGCTGGCGGT_________________GTGCAGGCTGCATGTCGGGGGAGCTGGCGGT TGTGGAGAGTGACCGAAG T ATP9B,AC125437.2 Ensembl:ENSG00000166377,Ensembl:ENSG00000279474 Protein coding,Other intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79146309..79146495 26863196 MeRIP-seq:(Medium) rs1318170666 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_5144570,Human_RBP_ID_5291796,Human_RBP_ID_5319640,Human_RBP_ID_5649338,Human_RBP_ID_8194743,Human_RBP_ID_21976927,Human_RBP_ID_22476107 RMVar_hsa_circ_190768,RMVar_hsa_circ_190754,RMVar_hsa_circ_190755,RMVar_hsa_circ_302324,RMVar_hsa_circ_307269,RMVar_hsa_circ_362154,RMVar_hsa_circ_305494,RMVar_hsa_circ_302316,RMVar_hsa_circ_277491,RMVar_hsa_circ_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190759,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_348318,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_190763,RMVar_hsa_circ_190764,RMVar_hsa_circ_35855,RMVar_hsa_circ_333566,RMVar_hsa_circ_276142,RMVar_hsa_circ_277985,RMVar_hsa_circ_292510,RMVar_hsa_circ_323815,RMVar_hsa_circ_289824,RMVar_hsa_circ_277723,RMVar_hsa_circ_273608,RMVar_hsa_circ_274684,RMVar_hsa_circ_66196,RMVar_hsa_circ_190772,RMVar_hsa_circ_6181,RMVar_hsa_circ_190773,RMVar_hsa_circ_190770,RMVar_hsa_circ_190771,RMVar_hsa_circ_190769,RMVar_hsa_circ_10883,RMVar_hsa_circ_318574,RMVar_hsa_circ_190766,RMVar_hsa_circ_190767,RMVar_hsa_circ_190765,RMVar_hsa_circ_354413,RMVar_hsa_circ_302656,RMVar_hsa_circ_305325,RMVar_hsa_circ_271759,RMVar_hsa_circ_190776,RMVar_hsa_circ_190777,RMVar_hsa_circ_190778 100232 RMVar_ID_100232 Human_SNP_ID_654625761 m1A Human chr18 - 79238314 79238314 79238314 AACTGACCTCCCCACAGCCTTGAGATGACAGCAGCATTCGGACAACAGCAGTCACGAGATTATTG AACTGACCTCCCCACAGCCTTGAGATGACAGCGGCATTCGGACAACAGCAGTCACGAGATTATTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79238188..79238315 26863196 MeRIP-seq:(Medium) rs954638362 Functional Loss SNV dbSNP153 33..33 33 - - - 100233 RMVar_ID_100233 Human_SNP_ID_654640854 m1A Human chr18 + 79297018 79296997 79297019 GAGAGAAGACACAGACGACCCAGAGAGAAGACAGAGACGACCCAGAGAGAAGACAGAGAGATGAC GAGAGAAGACAC______________________AGACGACCCAGAGAGAAGACAGAGAGATGAC CAGACGACCCAGAGAGAAGACAG C ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79297010..79297205 26863196 MeRIP-seq:(Medium) rs1458867623 Functional Loss DEL dbSNP153 13..34 33 - - - RMVar_hsa_circ_292324,RMVar_hsa_circ_190756,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_289824,RMVar_hsa_circ_66196,RMVar_hsa_circ_6181,RMVar_hsa_circ_190765,RMVar_hsa_circ_354413,RMVar_hsa_circ_369062,RMVar_hsa_circ_308055,RMVar_hsa_circ_190785,RMVar_hsa_circ_341106,RMVar_hsa_circ_190793,RMVar_hsa_circ_190797,RMVar_hsa_circ_326251,RMVar_hsa_circ_275811,RMVar_hsa_circ_190795,RMVar_hsa_circ_274331,RMVar_hsa_circ_371919,RMVar_hsa_circ_190796,RMVar_hsa_circ_360113,RMVar_hsa_circ_190798 100234 RMVar_ID_100234 Human_SNP_ID_654640954 m1A Human chr18 + 79297217 79297217 79297217 ACCCAGAGAGGAGACACAGACGACCCAGAGAGAAGACAGAGAGATGACCCAGAGAGGAGACGCAG ACCCAGAGAGGAGACACAGACGACCCAGAGAGGAGACAGAGAGATGACCCAGAGAGGAGACGCAG A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79296895..79297456 26863196 MeRIP-seq:(Medium) rs1174801832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292324,RMVar_hsa_circ_190756,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_289824,RMVar_hsa_circ_66196,RMVar_hsa_circ_6181,RMVar_hsa_circ_190765,RMVar_hsa_circ_354413,RMVar_hsa_circ_369062,RMVar_hsa_circ_308055,RMVar_hsa_circ_190785,RMVar_hsa_circ_341106,RMVar_hsa_circ_190793,RMVar_hsa_circ_190797,RMVar_hsa_circ_326251,RMVar_hsa_circ_275811,RMVar_hsa_circ_190795,RMVar_hsa_circ_274331,RMVar_hsa_circ_371919,RMVar_hsa_circ_190796,RMVar_hsa_circ_360113,RMVar_hsa_circ_190798 100235 RMVar_ID_100235 Human_SNP_ID_654644178 m1A Human chr18 + 79309505 79309505 79309505 GTGATCCCCAGCAGGTAGAAGGTCAGGGGTGGAGGAGTGATCTCCAGCAGGTAGAAGGTCAGGGG GTGATCCCCAGCAGGTAGAAGGTCAGGGGTGGTGGAGTGATCTCCAGCAGGTAGAAGGTCAGGGG A T ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79309472..79309551 26863196 MeRIP-seq:(Medium) rs1205747442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38186,RMVar_hsa_circ_66196,RMVar_hsa_circ_6181,RMVar_hsa_circ_190797,RMVar_hsa_circ_371919,RMVar_hsa_circ_360113,RMVar_hsa_circ_190800 100236 RMVar_ID_100236 Human_SNP_ID_654657926 m1A Human chr18 + 79356755 79356755 79356755 GGCCAGGGATTAGGGAGGAGGCAGCAGAGGGAAGTGGTTGCAGCTGCAGAGCAGCCGCAGGAGGG GGCCAGGGATTAGGGAGGAGGCAGCAGAGGGAGGTGGTTGCAGCTGCAGAGCAGCCGCAGGAGGG A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79356710..79356801 26863196 MeRIP-seq:(Medium) rs959236695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823447 RMVar_hsa_circ_38186,RMVar_hsa_circ_66196,RMVar_hsa_circ_190797,RMVar_hsa_circ_371919,RMVar_hsa_circ_63961 100237 RMVar_ID_100237 Human_SNP_ID_654670003 m1A Human chr18 - 79395677 79395660 79395677 GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCACGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGC_________________CCGGGGAGGGGGGCGC GGCGCCCCCCCTCCCCGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79395626..79395793 26863196 MeRIP-seq:(Medium) rs1255541327 Functional Loss DEL dbSNP153 33..49 33 - - - 100238 RMVar_ID_100238 Human_SNP_ID_654670021 m1A Human chr18 - 79395677 79395676 79395677 GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCACGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGC_CGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79395626..79395793 26863196 MeRIP-seq:(Medium) rs1182935776 Functional Loss DEL dbSNP153 33..33 33 - - - 100239 RMVar_ID_100239 Human_SNP_ID_654670023 m1A Human chr18 - 79395677 79395677 79395677 GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCACGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCGCGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79395626..79395793 26863196 MeRIP-seq:(Medium) rs1190030561 Functional Loss SNV dbSNP153 33..33 33 - - - 100240 RMVar_ID_100240 Human_SNP_ID_654670024 m1A Human chr18 - 79395677 79395677 79395677 GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCACGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC GGGAGGGGGGGCGCACGGGGAGGGGGGGGCGCCCGGGGAGGGGGGGCGCCCGGGGAGGGGGGCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79395626..79395793 26863196 MeRIP-seq:(Medium) rs1190030561 Functional Loss SNV dbSNP153 33..33 33 - - - 100241 RMVar_ID_100241 Human_SNP_ID_654670162 m1A Human chr18 + 79395957 79395957 79395957 GCCCTGCGTCAGAGCGAGACTCAGAGGCTCCGAACTCGCCGGCGGAGTCGCCGCGCCAGATCCCA GCCCTGCGTCAGAGCGAGACTCAGAGGCTCCGCACTCGCCGGCGGAGTCGCCGCGCCAGATCCCA A C NFATC1 Ensembl:ENSG00000131196 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79395906..79396004 26863196 MeRIP-seq:(Medium) rs1414191556 Functional Loss SNV dbSNP153 33..33 33 - - - 100242 RMVar_ID_100242 Human_SNP_ID_654746284 m1A Human chr18 - 79617412 79617410 79617412 GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGAGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGG__GGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79617405..79617532 26863196 MeRIP-seq:(Medium) rs1407493159 Functional Loss DEL dbSNP153 33..34 33 - - - 100243 RMVar_ID_100243 Human_SNP_ID_654746285 m1A Human chr18 - 79617412 79617411 79617412 GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGAGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGG_GGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79617405..79617532 26863196 MeRIP-seq:(Medium) rs1327430657 Functional Loss DEL dbSNP153 33..33 33 - - - 100244 RMVar_ID_100244 Human_SNP_ID_654746287 m1A Human chr18 - 79617412 79617412 79617412 GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGAGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79617405..79617532 26863196 MeRIP-seq:(Medium) rs1400264203 Functional Loss SNV dbSNP153 33..33 33 - - - 100245 RMVar_ID_100245 Human_SNP_ID_654746288 m1A Human chr18 - 79617412 79617412 79617412 GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGAGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG GGCGGGGTCCCGGGGGGGGCGGGGTCCCGGGGCGGGCGGGGTCCCGGGGGGGCGGGGTCCCGGGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79617405..79617532 26863196 MeRIP-seq:(Medium) rs1400264203 Functional Loss SNV dbSNP153 33..33 33 - - - 100246 RMVar_ID_100246 Human_SNP_ID_654766633 m1A Human chr18 + 79679900 79679867 79679900 GGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGAGCGCAGCGCAGGCCCCGTACCGACCGCCCGCC _________________________________GCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGA G CTDP1 Ensembl:ENSG00000060069 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:79679850..79680100;chr18:79679849..79680008 26863196 MeRIP-seq:(Medium) rs1341027180 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_4494055,Human_RBP_ID_5238116 100247 RMVar_ID_100247 Human_SNP_ID_654766637 m1A Human chr18 + 79679900 79679871 79679901 GGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGAGCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGTT______________________________CGCAGCGCAGGCCCCGTACCGACCGCCCGCC TGTGTCGCCGCGGTAGGCGCTGCGCTCTGAG T CTDP1 Ensembl:ENSG00000060069 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:79679850..79680100;chr18:79679849..79680008 26863196 MeRIP-seq:(Medium) rs1245709346 Functional Loss DEL dbSNP153 5..34 33 - - - Human_RBP_ID_4494055,Human_RBP_ID_5238116 100248 RMVar_ID_100248 Human_SNP_ID_654766645 m1A Human chr18 + 79679900 79679886 79679900 GGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGAGCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGTTGTGTCGCCGCGGTAG______________GCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGCGCTGCGCTCTGA G CTDP1 Ensembl:ENSG00000060069 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:79679850..79680100;chr18:79679849..79680008 26863196 MeRIP-seq:(Medium) rs1448606399 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_4494055,Human_RBP_ID_5238116 100249 RMVar_ID_100249 Human_SNP_ID_654766654 m1A Human chr18 + 79679900 79679896 79679901 GGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGAGCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGTTGTGTCGCCGCGGTAGGCGCTGCGCT_____CGCAGCGCAGGCCCCGTACCGACCGCCCGCC TCTGAG T CTDP1 Ensembl:ENSG00000060069 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:79679850..79680100;chr18:79679849..79680008 26863196 MeRIP-seq:(Medium) rs1033949487 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_4494055,Human_RBP_ID_5238116 100250 RMVar_ID_100250 Human_SNP_ID_654766663 m1A Human chr18 + 79679900 79679897 79679901 GGTTGTGTCGCCGCGGTAGGCGCTGCGCTCTGAGCGCAGCGCAGGCCCCGTACCGACCGCCCGCC GGTTGTGTCGCCGCGGTAGGCGCTGCGCTC____CGCAGCGCAGGCCCCGTACCGACCGCCCGCC CTGAG C CTDP1 Ensembl:ENSG00000060069 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr18:79679850..79680100;chr18:79679849..79680008 26863196 MeRIP-seq:(Medium) rs1444407240 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_4494055,Human_RBP_ID_5238116 100251 RMVar_ID_100251 Human_SNP_ID_654766716 m1A Human chr18 - 79679974 79679974 79679974 GCCACAGCCGCCGTCGGGGCGCCCTCGGCAGGAACGCGACCCGCGGCCGGCACCTCCATCGCGGA GCCACAGCCGCCGTCGGGGCGCCCTCGGCAGGCACGCGACCCGCGGCCGGCACCTCCATCGCGGA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:79679872..79680107 26863410 MeRIP-seq:(Medium) rs771179575 Functional Loss SNV dbSNP153 33..33 33 - - - 100252 RMVar_ID_100252 Human_SNP_ID_654777934 m1A Human chr18 + 79715130 79715130 79715130 CGGCTGTGCCGACAGGAAGGAGGCGGAGACCGAGTCACAGAACAGCGAGCTGTCGGGGGTCACTG CGGCTGTGCCGACAGGAAGGAGGCGGAGACCGTGTCACAGAACAGCGAGCTGTCGGGGGTCACTG A T CTDP1 Ensembl:ENSG00000060069 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79714937..79715288 26863196 MeRIP-seq:(Medium) rs762909226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18993820,Human_RBP_ID_22064570 RMVar_hsa_circ_52995,RMVar_hsa_circ_190810,RMVar_hsa_circ_342960,RMVar_hsa_circ_360513,RMVar_hsa_circ_308953,RMVar_hsa_circ_190809 100253 RMVar_ID_100253 Human_SNP_ID_654781828 m1A Human chr18 - 79726908 79726908 79726908 CCACAGACGTCCACCAGCAACGGCGTCATCCCACCCCGACAGCCATCCACCAGCAACGGCGTCAC CCACAGACGTCCACCAGCAACGGCGTCATCCCCCCCCGACAGCCATCCACCAGCAACGGCGTCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79726902..79727075 26863196 MeRIP-seq:(Medium) rs1015366287 Functional Loss SNV dbSNP153 33..33 33 - - - 100254 RMVar_ID_100254 Human_SNP_ID_654782027 m1A Human chr18 + 79727386 79727363 79727386 GGGAAGCGTGGCGTTCACGGGATGGAAAGCGCAGCGTTCACGGTGTTCACGGGATGGGAAGCGCA GGGAAGCGTG_______________________GCGTTCACGGTGTTCACGGGATGGGAAGCGCA GGCGTTCACGGGATGGAAAGCGCA G CTDP1 Ensembl:ENSG00000060069 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79727382..79727466 26863196 MeRIP-seq:(Medium) rs1020494163 Functional Loss DEL dbSNP153 11..33 33 - - - RMVar_hsa_circ_190810,RMVar_hsa_circ_342960,RMVar_hsa_circ_308953,RMVar_hsa_circ_190809 100255 RMVar_ID_100255 Human_SNP_ID_654782038 m1A Human chr18 + 79727386 79727386 79727386 GGGAAGCGTGGCGTTCACGGGATGGAAAGCGCAGCGTTCACGGTGTTCACGGGATGGGAAGCGCA GGGAAGCGTGGCGTTCACGGGATGGAAAGCGCGGCGTTCACGGTGTTCACGGGATGGGAAGCGCA A G CTDP1 Ensembl:ENSG00000060069 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79727382..79727466 26863196 MeRIP-seq:(Medium) rs190501266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190810,RMVar_hsa_circ_342960,RMVar_hsa_circ_308953,RMVar_hsa_circ_190809 100256 RMVar_ID_100256 Human_SNP_ID_654782056 m1A Human chr18 - 79727426 79727426 79727426 ACGAACACCGTGAATGCCAGGCTTCCCACCCCACGAACGCTGCGCTTCCCATCCCGTGAACACCG ACGAACACCGTGAATGCCAGGCTTCCCACCCCCCGAACGCTGCGCTTCCCATCCCGTGAACACCG T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:79727376..79727538 26863196 MeRIP-seq:(Medium) rs1252067276 Functional Loss SNV dbSNP153 33..33 33 - - - 100257 RMVar_ID_100257 Human_SNP_ID_654790709 m1A Human chr18 - 79753786 79753784 79753786 GGCTTCAGTCCCTGCCCGCTGCCCGCGCTCACATGAGGTCGTTGAGCTCCGCCTCCAGCGCCTTG GGCTTCAGTCCCTGCCCGCTGCCCGCGCTCAC__GAGGTCGTTGAGCTCCGCCTCCAGCGCCTTG CAT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:79753736..79753837 32194978 MeRIP-seq:(Medium) rs765172459 Functional Loss DEL dbSNP153 33..34 33 - - - 100258 RMVar_ID_100258 Human_SNP_ID_654790710 m1A Human chr18 - 79753786 79753786 79753786 GGCTTCAGTCCCTGCCCGCTGCCCGCGCTCACATGAGGTCGTTGAGCTCCGCCTCCAGCGCCTTG GGCTTCAGTCCCTGCCCGCTGCCCGCGCTCACGTGAGGTCGTTGAGCTCCGCCTCCAGCGCCTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:79753736..79753837 32194978 MeRIP-seq:(Medium) rs771431554 Functional Loss SNV dbSNP153 33..33 33 - - - 100259 RMVar_ID_100259 Human_SNP_ID_654833901 m1A Human chr18 + 79902967 79902967 79902967 CAGGATGCGGCAGGCCCCAGTACCCCCCACTCAGGAATTTGCTTCAGGCCAAAAGCCCAGGGCAG CAGGATGCGGCAGGCCCCAGTACCCCCCACTCGGGAATTTGCTTCAGGCCAAAAGCCCAGGGCAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:79902767..79902967 32194978 MeRIP-seq:(Medium) rs1423696690 Functional Loss SNV dbSNP153 33..33 33 - - - 100260 RMVar_ID_100260 Human_SNP_ID_654833906 m1A Human chr18 + 79902988 79902988 79902988 ACCCCCCACTCAGGAATTTGCTTCAGGCCAAAAGCCCAGGGCAGCAGGGTAAGGCGCCATCGGCC ACCCCCCACTCAGGAATTTGCTTCAGGCCAAAGGCCCAGGGCAGCAGGGTAAGGCGCCATCGGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:79902867..79903067 32194978 MeRIP-seq:(Medium) rs945726611 Functional Loss SNV dbSNP153 33..33 33 - - - 100261 RMVar_ID_100261 Human_SNP_ID_654834352 m1A Human chr18 - 79904182 79904182 79904182 CACCGCTGACCGCCTGCTTGTGTCTCCACAGCATCAAGATGGTGCTCATGTGGACCAGTGGTGAC CACCGCTGACCGCCTGCTTGTGTCTCCACAGCTTCAAGATGGTGCTCATGTGGACCAGTGGTGAC T A SLC66A2 Ensembl:ENSG00000122490 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:79904160..79915464 32194978 MeRIP-seq:(Medium) rs1427314584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1927520,Human_Splice_Rec_1927530,Human_Splice_Rec_1927540,Human_Splice_Rec_1927548,Human_Splice_Rec_1927558,Human_Splice_Rec_1927564,Human_Splice_Rec_1927566,Human_Splice_Rec_1927570,Human_Splice_Rec_1927578 RMVar_hsa_circ_190814,RMVar_hsa_circ_79832 100262 RMVar_ID_100262 Human_SNP_ID_654835862 m1A Human chr18 + 79909508 79909508 79909508 CCAACCTTCCCCACAACCTCACCAGAGTCCCCAGCCTTCCCCACAACATCACCACAGAGTCCCCA CCAACCTTCCCCACAACCTCACCAGAGTCCCCGGCCTTCCCCACAACATCACCACAGAGTCCCCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:79909378..79909547 26863196 MeRIP-seq:(Medium) rs1007504901 Functional Loss SNV dbSNP153 33..33 33 - - - 100263 RMVar_ID_100263 Human_SNP_ID_654837322 m1A Human chr18 + 79913190 79913186 79913190 ACCATGCCACACCTGCCTGGTCACCCATCCTCACTCAGCCACGGTGGTCACACACTGTCGGGGTC ACCATGCCACACCTGCCTGGTCACCCATC____CTCAGCCACGGTGGTCACACACTGTCGGGGTC CCTCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79913187..79913330 26863196 MeRIP-seq:(Medium) rs917661603 Functional Loss DEL dbSNP153 30..33 33 - - - 100264 RMVar_ID_100264 Human_SNP_ID_654838252 m1A Human chr18 + 79916036 79916036 79916036 TAGCCGCAGTGCTCCCGTACCCTCCCATACCCACGGTGCTCCCGTACCCATGGCGCTCCCATACC TAGCCGCAGTGCTCCCGTACCCTCCCATACCCGCGGTGCTCCCGTACCCATGGCGCTCCCATACC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:79915931..79916152 26863196 MeRIP-seq:(Medium) rs1302503175 Functional Loss SNV dbSNP153 33..33 33 - - - 100265 RMVar_ID_100265 Human_SNP_ID_654838266 m1A Human chr18 - 79916048 79916048 79916048 GGGAGCGCTGTGGGTATGGGAGCGCCATGGGTACGGGAGCACCGTGGGTATGGGAGGGTACGGGA GGGAGCGCTGTGGGTATGGGAGCGCCATGGGTTCGGGAGCACCGTGGGTATGGGAGGGTACGGGA T A SLC66A2 Ensembl:ENSG00000122490 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79915963..79916362 26863196 MeRIP-seq:(Medium) rs1006928984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262945,Human_RBP_ID_3561122,Human_RBP_ID_5189585,Human_RBP_ID_5319566,Human_RBP_ID_8095375,Human_RBP_ID_8194228,Human_RBP_ID_8232756,Human_RBP_ID_8727805,Human_RBP_ID_8942047,Human_RBP_ID_9424776,Human_RBP_ID_18420768,Human_RBP_ID_18460802,Human_RBP_ID_18944169,Human_RBP_ID_22416487,Human_RBP_ID_22718006,Human_RBP_ID_24552642,Human_RBP_ID_26783182 RMVar_hsa_circ_190814,RMVar_hsa_circ_79832 100266 RMVar_ID_100266 Human_SNP_ID_654838267 m1A Human chr18 - 79916048 79916048 79916048 GGGAGCGCTGTGGGTATGGGAGCGCCATGGGTACGGGAGCACCGTGGGTATGGGAGGGTACGGGA GGGAGCGCTGTGGGTATGGGAGCGCCATGGGTGCGGGAGCACCGTGGGTATGGGAGGGTACGGGA T C SLC66A2 Ensembl:ENSG00000122490 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79915963..79916362 26863196 MeRIP-seq:(Medium) rs1006928984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262945,Human_RBP_ID_3561122,Human_RBP_ID_5189585,Human_RBP_ID_5319566,Human_RBP_ID_8095375,Human_RBP_ID_8194228,Human_RBP_ID_8232756,Human_RBP_ID_8727805,Human_RBP_ID_8942047,Human_RBP_ID_9424776,Human_RBP_ID_18420768,Human_RBP_ID_18460802,Human_RBP_ID_18944169,Human_RBP_ID_22416487,Human_RBP_ID_22718006,Human_RBP_ID_24552642,Human_RBP_ID_26783182 RMVar_hsa_circ_190814,RMVar_hsa_circ_79832 100267 RMVar_ID_100267 Human_SNP_ID_654839572 m1A Human chr18 - 79919247 79919247 79919247 GGAGACCCTGGGCTTCCTGGCTGTGCTGACCGAAGCCATGCTGGGTGTGCCCCAGCTTTACCGCA GGAGACCCTGGGCTTCCTGGCTGTGCTGACCGCAGCCATGCTGGGTGTGCCCCAGCTTTACCGCA T G SLC66A2 Ensembl:ENSG00000122490 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr18:79919232..79924918 32194978 MeRIP-seq:(Medium) rs1374622182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8232838,Human_RBP_ID_24374341 Human_Splice_Rec_1927519,Human_Splice_Rec_1927529,Human_Splice_Rec_1927539,Human_Splice_Rec_1927547,Human_Splice_Rec_1927569,Human_Splice_Rec_1927577 RMVar_hsa_circ_44795,RMVar_hsa_circ_190814,RMVar_hsa_circ_79832,RMVar_hsa_circ_298289 100268 RMVar_ID_100268 Human_SNP_ID_654848680 m1A Human chr18 + 79950977 79950977 79950977 GAGGCTGTCACGGGCTCCGCGCCCCGCGGGCCACCGGCCGCCTGCTCATCGCCGCTCCGCGCGCT GAGGCTGTCACGGGCTCCGCGCCCCGCGGGCCTCCGGCCGCCTGCTCATCGCCGCTCCGCGCGCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79950926..79951054 26863196 MeRIP-seq:(Medium) rs1175789058 Functional Loss SNV dbSNP153 33..33 33 - - - 100269 RMVar_ID_100269 Human_SNP_ID_654848830 m1A Human chr18 - 79951297 79951297 79951297 CCCTCCCCCACCCCATCCCGGGGCGCGCGTGGACCCCCGCCGGCTAAGCGCACCCGGGCGGTGAC CCCTCCCCCACCCCATCCCGGGGCGCGCGTGGGCCCCCGCCGGCTAAGCGCACCCGGGCGGTGAC T C SLC66A2 Ensembl:ENSG00000122490 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:79951288..79951622 26863196 MeRIP-seq:(Medium) rs1419177939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5369256 100270 RMVar_ID_100270 Human_SNP_ID_654848966 m1A Human chr18 + 79951603 79951603 79951603 CGCTCCTTACCTGCGCCCCCAGCCCCGCGCCCAGCGCCCCGCGTCCCCGCGCCGCTGACCCGCGC CGCTCCTTACCTGCGCCCCCAGCCCCGCGCCCTGCGCCCCGCGTCCCCGCGCCGCTGACCCGCGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:79950909..79951645 26863196 MeRIP-seq:(Medium) rs545380076 Functional Loss SNV dbSNP153 33..33 33 - - - 100271 RMVar_ID_100271 Human_SNP_ID_654849149 m1A Human chr18 - 79951928 79951928 79951928 GCGTCCGGACCCCGCGCCCCCGGCCCTCCAGGACGACGCCCTCCGCTTGGATGGCCGCGCGCCGG GCGTCCGGACCCCGCGCCCCCGGCCCTCCAGGGCGACGCCCTCCGCTTGGATGGCCGCGCGCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:79951886..79952059 26863196 MeRIP-seq:(Medium) rs1466094187 Functional Loss SNV dbSNP153 33..33 33 - - - 100272 RMVar_ID_100272 Human_SNP_ID_654849318 m1A Human chr18 + 79952489 79952489 79952489 GGTGAGGACTGAGGGCGAGGGGCGCGTGGATGAGGGGCGCGCGGGTGAAGAGTGAGGGGAGCGCG GGTGAGGACTGAGGGCGAGGGGCGCGTGGATGGGGGGCGCGCGGGTGAAGAGTGAGGGGAGCGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr18:79952335..79952811;chr18:79952309..79952895 26863196 MeRIP-seq:(Medium) rs1352234769 Functional Loss SNV dbSNP153 33..33 33 - - - 100273 RMVar_ID_100273 Human_SNP_ID_654849335 m1A Human chr18 + 79952516 79952516 79952516 GGATGAGGGGCGCGCGGGTGAAGAGTGAGGGGAGCGCGGGTGAAGTGTGAGGGGAGCGCGGGTGA GGATGAGGGGCGCGCGGGTGAAGAGTGAGGGGCGCGCGGGTGAAGTGTGAGGGGAGCGCGGGTGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79952311..79952562 26863196 MeRIP-seq:(Medium) rs868437352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23778584 100274 RMVar_ID_100274 Human_SNP_ID_654852855 m1A Human chr18 + 79964698 79964698 79964698 TGTCGCCACCTCGCGCCGGGTCCGCGCGGCCCACGGGACCCCCCACTGACGCCCCCGGCCAGCGG TGTCGCCACCTCGCGCCGGGTCCGCGCGGCCCGCGGGACCCCCCACTGACGCCCCCGGCCAGCGG A G HSBP1L1 Ensembl:ENSG00000226742 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr18:79964651..79966650;chr18:79964651..79966631 26863196 MeRIP-seq:(Medium) rs964171371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511075,Human_RBP_ID_4494510,Human_RBP_ID_18420683 Human_Splice_Rec_1927621,Human_Splice_Rec_1927623,Human_Splice_Rec_1927629 100275 RMVar_ID_100275 Human_SNP_ID_654852856 m1A Human chr18 + 79964698 79964698 79964698 TGTCGCCACCTCGCGCCGGGTCCGCGCGGCCCACGGGACCCCCCACTGACGCCCCCGGCCAGCGG TGTCGCCACCTCGCGCCGGGTCCGCGCGGCCCTCGGGACCCCCCACTGACGCCCCCGGCCAGCGG A T HSBP1L1 Ensembl:ENSG00000226742 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr18:79964651..79966650;chr18:79964651..79966631 26863196 MeRIP-seq:(Medium) rs964171371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511075,Human_RBP_ID_4494510,Human_RBP_ID_18420683 Human_Splice_Rec_1927621,Human_Splice_Rec_1927623,Human_Splice_Rec_1927629 100276 RMVar_ID_100276 Human_SNP_ID_654859784 m1A Human chr18 - 79988392 79988392 79988392 CGCCTTGGGCGGCGGCGAGCGCGCGGGCCGCCATGTCGTACATGCTCCCGCACCTGCACAACGGC CGCCTTGGGCGGCGGCGAGCGCGCGGGCCGCCGTGTCGTACATGCTCCCGCACCTGCACAACGGC T C TXNL4A Ensembl:ENSG00000141759 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79988344..79988511 26863196 MeRIP-seq:(Medium) rs1281458263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4492918,Human_RBP_ID_5238142,Human_RBP_ID_5319568,Human_RBP_ID_8942049,Human_RBP_ID_9327797,Human_RBP_ID_26980791 100277 RMVar_ID_100277 Human_SNP_ID_654859785 m1A Human chr18 - 79988392 79988392 79988392 CGCCTTGGGCGGCGGCGAGCGCGCGGGCCGCCATGTCGTACATGCTCCCGCACCTGCACAACGGC CGCCTTGGGCGGCGGCGAGCGCGCGGGCCGCCCTGTCGTACATGCTCCCGCACCTGCACAACGGC T G TXNL4A Ensembl:ENSG00000141759 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79988344..79988511 26863196 MeRIP-seq:(Medium) rs1281458263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4492918,Human_RBP_ID_5238142,Human_RBP_ID_5319568,Human_RBP_ID_8942049,Human_RBP_ID_9327797,Human_RBP_ID_26980791 100278 RMVar_ID_100278 Human_SNP_ID_654859805 m1A Human chr18 + 79988432 79988432 79988432 CGCGCGCTCGCCGCCGCCCAAGGCGGGGCGCCAGGGAGGGCCCAGCGAGGTGGGCTCAGCCGGCC CGCGCGCTCGCCGCCGCCCAAGGCGGGGCGCCTGGGAGGGCCCAGCGAGGTGGGCTCAGCCGGCC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:79988392..79988550 26863196 MeRIP-seq:(Medium) rs776362969 Functional Loss SNV dbSNP153 33..33 33 - - - 100279 RMVar_ID_100279 Human_SNP_ID_654871627 m1A Human chr18 - 80034539 80034539 80034539 GCGCAGCATCGCGGCTACGGAACAGGGCCCGGAGACCCGCGCGGGAGCGCCACAGCCCGCCCGCC GCGCAGCATCGCGGCTACGGAACAGGGCCCGGTGACCCGCGCGGGAGCGCCACAGCCCGCCCGCC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:80034416..80034675 26863410 MeRIP-seq:(Medium) rs1234012901 Functional Loss SNV dbSNP153 33..33 33 - - - 100280 RMVar_ID_100280 Human_SNP_ID_654871665 m1A Human chr18 - 80034601 80034601 80034601 CTTGAGCCAGTTCTTGCAGGAGACAGCAGAGCAGTGAAGTCCCCGCTCGCAGCCTGGAAATAGCG CTTGAGCCAGTTCTTGCAGGAGACAGCAGAGCCGTGAAGTCCCCGCTCGCAGCCTGGAAATAGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:80034483..80034600 26863196 MeRIP-seq:(Medium) rs1011615498 Functional Loss SNV dbSNP153 33..33 33 - - - 100281 RMVar_ID_100281 Human_SNP_ID_654874883 m1A Human chr18 - 80045930 80045930 80045930 TTCCTTCCCTTTTTCATCTGCGTTGTCAGCTCAGCCACCTGCCCCTGCCACACCAGGCCCCCGAG TTCCTTCCCTTTTTCATCTGCGTTGTCAGCTCGGCCACCTGCCCCTGCCACACCAGGCCCCCGAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:80045847..80046157 26863196 MeRIP-seq:(Medium) rs1403335734 Functional Loss SNV dbSNP153 33..33 33 - - - 100282 RMVar_ID_100282 Human_SNP_ID_654874911 m1A Human chr18 + 80046001 80046000 80046002 CAAGCCCCGCCTGGAGCAGGACAGCTCCCTCAAGAGTTACCTGTCAGGCGAGGAGGTTGAAGATG CAAGCCCCGCCTGGAGCAGGACAGCTCCCTCA__AGTTACCTGTCAGGCGAGGAGGTTGAAGATG AAG A RBFA,AC090360.1 Ensembl:ENSG00000101546,Ensembl:ENSG00000267127 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:80045801..80046000 32194978 MeRIP-seq:(Medium) rs1568390445 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5319652,Human_RBP_ID_18993827 Human_Splice_Rec_1927701 RMVar_hsa_circ_190821 100283 RMVar_ID_100283 Human_SNP_ID_654874942 m1A Human chr18 + 80046070 80046070 80046070 GGACCTGGTTGGTGCCCCGGAGTACGAATGCTATGCCCCGGACACAGAGGAGTTGGAGGCAGAGA GGACCTGGTTGGTGCCCCGGAGTACGAATGCTCTGCCCCGGACACAGAGGAGTTGGAGGCAGAGA A C RBFA,AC090360.1 Ensembl:ENSG00000101546,Ensembl:ENSG00000267127 Protein coding,Protein coding CDS,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:80046033..80046166 26863196 MeRIP-seq:(Medium) rs150406097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238701,Human_RBP_ID_906055,Human_RBP_ID_9379701,Human_RBP_ID_17655276,Human_RBP_ID_18165106,Human_RBP_ID_18993506,Human_RBP_ID_22064283,Human_RBP_ID_26334743 RMVar_hsa_circ_190821 100284 RMVar_ID_100284 Human_SNP_ID_654874943 m1A Human chr18 + 80046070 80046070 80046070 GGACCTGGTTGGTGCCCCGGAGTACGAATGCTATGCCCCGGACACAGAGGAGTTGGAGGCAGAGA GGACCTGGTTGGTGCCCCGGAGTACGAATGCTGTGCCCCGGACACAGAGGAGTTGGAGGCAGAGA A G RBFA,AC090360.1 Ensembl:ENSG00000101546,Ensembl:ENSG00000267127 Protein coding,Protein coding CDS,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:80046033..80046166 26863196 MeRIP-seq:(Medium) rs150406097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238701,Human_RBP_ID_906055,Human_RBP_ID_9379701,Human_RBP_ID_17655276,Human_RBP_ID_18165106,Human_RBP_ID_18993506,Human_RBP_ID_22064283,Human_RBP_ID_26334743 RMVar_hsa_circ_190821 100285 RMVar_ID_100285 Human_SNP_ID_654874976 m1A Human chr18 + 80046147 80046147 80046147 GAACAGAGGATGGCCACAGCTGCGGAGCAAGCAGGGAGTAGATGGAGAGGCTCTGCCCATCCCAC GAACAGAGGATGGCCACAGCTGCGGAGCAAGCGGGGAGTAGATGGAGAGGCTCTGCCCATCCCAC A G RBFA,AC090360.1 Ensembl:ENSG00000101546,Ensembl:ENSG00000267127 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:80046098..80046298 32194978 MeRIP-seq:(Medium) rs1186403039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17655276,Human_RBP_ID_22064582,Human_RBP_ID_26334744 RMVar_hsa_circ_190821 100286 RMVar_ID_100286 Human_SNP_ID_654891161 m1A Human chr18 - 80109344 80109344 80109344 CGCCCGCCCGCGCCTCCGCCCCGCGCGGCGGGACCCCCGCCTCAGCGCGCGCCCACCCCCAGCGC CGCCCGCCCGCGCCTCCGCCCCGCGCGGCGGGCCCCCCGCCTCAGCGCGCGCCCACCCCCAGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:80109276..80109450 26863196 MeRIP-seq:(Medium) rs954196530 Functional Loss SNV dbSNP153 33..33 33 - - - 100287 RMVar_ID_100287 Human_SNP_ID_654898708 m1A Human chr18 - 80136414 80136412 80136414 GGCTGTTCTGGCCCACAGGCAGAGGGCTGGAGACCAGAGTCATGTGGGATTGGCCAGCAGCAGGG GGCTGTTCTGGCCCACAGGCAGAGGGCTGGAG__CAGAGTCATGTGGGATTGGCCAGCAGCAGGG GGT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:80136145..80136545 32194978 MeRIP-seq:(Medium) rs764942256 Functional Loss DEL dbSNP153 33..34 33 - - - 100288 RMVar_ID_100288 Human_SNP_ID_654899003 m1A Human chr18 + 80137044 80137044 80137044 TGTAAACCAGGGTGTGAATTCTGGTGTTCTGCAGCTTAGTCAGCCTGTTGTGTCGGGAGTTCTTC TGTAAACCAGGGTGTGAATTCTGGTGTTCTGCGGCTTAGTCAGCCTGTTGTGTCGGGAGTTCTTC A G ADNP2 Ensembl:ENSG00000101544 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:80136994..80137244 32194978 MeRIP-seq:(Medium) rs1187825702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1552245,Human_RBP_ID_1878686,Human_RBP_ID_8474893,Human_RBP_ID_8828519,Human_RBP_ID_13341994,Human_RBP_ID_17497405,Human_RBP_ID_18720390 RMVar_hsa_circ_113916,RMVar_hsa_circ_190825 100289 RMVar_ID_100289 Human_SNP_ID_654902828 m1A Human chr18 + 80151087 80151087 80151087 AGTGGGGCTGGGAGGCTGAGAGGTAGCTGTGAAGGGGCATCGGGCCTGGAGATGGGGGAGGGCAC AGTGGGGCTGGGAGGCTGAGAGGTAGCTGTGAGGGGGCATCGGGCCTGGAGATGGGGGAGGGCAC A G PARD6G-AS1 Ensembl:ENSG00000267270 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:80150992..80151167 26863196 MeRIP-seq:(Medium) rs962542617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6707570,Human_RBP_ID_8194482,Human_RBP_ID_9424976,Human_RBP_ID_23778899 100290 RMVar_ID_100290 Human_SNP_ID_654912372 m1A Human chr18 + 80186118 80186118 80186118 ATATACAGTCACATATGCTTGCACACCCTCACACGCACCCACACATGCGTATACCCTCACGCGGG ATATACAGTCACATATGCTTGCACACCCTCACGCGCACCCACACATGCGTATACCCTCACGCGGG A G AC139100.1 Ensembl:ENSG00000267251 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:80186049..80186138 26863196 MeRIP-seq:(Medium) rs1209805452 Functional Loss SNV dbSNP153 33..33 33 - - - 100291 RMVar_ID_100291 Human_SNP_ID_632723669 m1A Human chr17 + 75003299 75003299 75003299 CCTGGTGGGGGCGCTGCGCTCCCAGGTGAGCCAGGAGCGGCAGCGCAAGGAGCGGGCGGAGCGCG CCTGGTGGGGGCGCTGCGCTCCCAGGTGAGCCGGGAGCGGCAGCGCAAGGAGCGGGCGGAGCGCG A G CDR2L Ensembl:ENSG00000109089 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75003250..75003366 26863196 MeRIP-seq:(Medium) rs1299385789 Functional Loss SNV dbSNP153 33..33 33 - - - 100292 RMVar_ID_100292 Human_SNP_ID_632724126 m1A Human chr17 + 75004350 75004349 75004350 CCCCACTACCCCAGGGATCCCCCAGCTCCCCCAGCCCCTGGCTTCCTGACCCTGCGCCTCACCCT CCCCACTACCCCAGGGATCCCCCAGCTCCCCC_GCCCCTGGCTTCCTGACCCTGCGCCTCACCCT CA C CDR2L Ensembl:ENSG00000109089 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75004152..75004400 26863196 MeRIP-seq:(Medium) rs1304343143 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_499243,Human_RBP_ID_27456636 Human_miRNA_ID_1357925,Human_miRNA_ID_1478402 100293 RMVar_ID_100293 Human_SNP_ID_632724238 m1A Human chr17 - 75004858 75004858 75004858 GCTCCCCACTGCCCCGGCCCCTGGAAAGCTTAAGGCCCAGCAGGCATTTCTGGGGTTGGAAGCCA GCTCCCCACTGCCCCGGCCCCTGGAAAGCTTAGGGCCCAGCAGGCATTTCTGGGGTTGGAAGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75004808..75005037 26863196 MeRIP-seq:(Medium) rs1299564376 Functional Loss SNV dbSNP153 33..33 33 - - - 100294 RMVar_ID_100294 Human_SNP_ID_632724442 m1A Human chr17 + 75005651 75005651 75005651 TGTGTCTGTTATCTGGGGGAGAGGAGTGTGGAAGGGTTGGGGGAAGAGCTCCAGCCTGTCTGCTC TGTGTCTGTTATCTGGGGGAGAGGAGTGTGGATGGGTTGGGGGAAGAGCTCCAGCCTGTCTGCTC A T CDR2L Ensembl:ENSG00000109089 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75005600..75005700 32194978 MeRIP-seq:(Medium) rs192319454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499256,Human_RBP_ID_6642332,Human_RBP_ID_18296290,Human_RBP_ID_26458192 100295 RMVar_ID_100295 Human_SNP_ID_632726225 m1A Human chr17 - 75012904 75012904 75012904 GGGTTCCTAACGTCACCCAGCAGCCTGACAAAACGCCCCTTCCGTCCAGTCCTTCCCGGCTCACC GGGTTCCTAACGTCACCCAGCAGCCTGACAAAGCGCCCCTTCCGTCCAGTCCTTCCCGGCTCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75012893..75013090 26863196 MeRIP-seq:(Medium) rs1385073475 Functional Loss SNV dbSNP153 33..33 33 - - - 100296 RMVar_ID_100296 Human_SNP_ID_632726513 m1A Human chr17 - 75014002 75014002 75014002 CCTACATTGCAATCTCCTTACTTGTCTCCCTGATCTTGGCATCCTCTATCTGTTCTCTGTAAGGC CCTACATTGCAATCTCCTTACTTGTCTCCCTGGTCTTGGCATCCTCTATCTGTTCTCTGTAAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75014000..75014137 26863196 MeRIP-seq:(Medium) rs889601986 Functional Loss SNV dbSNP153 33..33 33 - - - 100297 RMVar_ID_100297 Human_SNP_ID_632726515 m1A Human chr17 + 75014010 75014010 75014010 GAGAACAGATAGAGGATGCCAAGATCAGGGAGACAAGTAAGGAGATTGCAATGTAGGGCAAGAGA GAGAACAGATAGAGGATGCCAAGATCAGGGAGGCAAGTAAGGAGATTGCAATGTAGGGCAAGAGA A G MRPL58 Ensembl:ENSG00000167862 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75013985..75014135 26863196 MeRIP-seq:(Medium) rs1023649998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13157060,Human_RBP_ID_23748388 RMVar_hsa_circ_78525,RMVar_hsa_circ_109022,RMVar_hsa_circ_186943,RMVar_hsa_circ_186944 100298 RMVar_ID_100298 Human_SNP_ID_632726941 m1A Human chr17 + 75015540 75015537 75015541 ATTTTCATCAGCATAGATGAAGTATTCTAGAGAAAGAAAGAGGAGAGAGAGAGAAGTATTTCAAG ATTTTCATCAGCATAGATGAAGTATTCTAG____AGAAAGAGGAGAGAGAGAGAAGTATTTCAAG GAGAA G MRPL58 Ensembl:ENSG00000167862 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75015537..75015666 26863196 MeRIP-seq:(Medium) rs1466100683 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_78525,RMVar_hsa_circ_109022,RMVar_hsa_circ_186943,RMVar_hsa_circ_186944 100299 RMVar_ID_100299 Human_SNP_ID_632732186 m1A Human chr17 - 75034446 75034446 75034446 ACTGGCCTCCTAAGCCAGGGATTGTGGGTTCGAGTCCCACCTGGGGTGTCGAGAGGGGCTGTGCT ACTGGCCTCCTAAGCCAGGGATTGTGGGTTCGTGTCCCACCTGGGGTGTCGAGAGGGGCTGTGCT T A tRNA-Arg-CCT-2-1 RNACentral:URS0000390F3A tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq;HEPG2 cell line,mRNA untreated chr17:75034371..75034478 29072297,31548705,31548705,26863196 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs111249217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499276,Human_RBP_ID_1369762,Human_RBP_ID_1541648,Human_RBP_ID_1868789,Human_RBP_ID_3536848,Human_RBP_ID_5260658,Human_RBP_ID_6642366,Human_RBP_ID_8253676,Human_RBP_ID_8462653,Human_RBP_ID_8822081,Human_RBP_ID_9076167,Human_RBP_ID_17692991,Human_RBP_ID_18708196,Human_RBP_ID_20267685,Human_RBP_ID_22806616,Human_RBP_ID_22960032,Human_RBP_ID_23129670,Human_RBP_ID_23748407,Human_RBP_ID_24417530,Human_RBP_ID_24481775 100300 RMVar_ID_100300 Human_SNP_ID_632733823 m1A Human chr17 - 75039202 75039202 75039202 CCAGGATTGTAGAATATGAGAAAGAGGTAAGGATGATGGGTAGCCGTTGCCTATAATATGGGTTC CCAGGATTGTAGAATATGAGAAAGAGGTAAGGGTGATGGGTAGCCGTTGCCTATAATATGGGTTC T C ATP5PD Ensembl:ENSG00000167863 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75039201..75039250 32194978 MeRIP-seq:(Medium) rs756581780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19079862 Human_Splice_Rec_1864444,Human_Splice_Rec_1864452,Human_Splice_Rec_1864462 RMVar_hsa_circ_186950,RMVar_hsa_circ_84447,RMVar_hsa_circ_108909,RMVar_hsa_circ_186951 100301 RMVar_ID_100301 Human_SNP_ID_632734079 m1A Human chr17 + 75040153 75040153 75040153 CAGTATATTTATCCTCTGGCACGGGAACCTTCAGCGCATTAAACTACAAACACAAGGGCACGGGA CAGTATATTTATCCTCTGGCACGGGAACCTTCCGCGCATTAAACTACAAACACAAGGGCACGGGA A C KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75040042..75040203 26863196 MeRIP-seq:(Medium) rs371625622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1864388 100302 RMVar_ID_100302 Human_SNP_ID_632734080 m1A Human chr17 + 75040153 75040153 75040153 CAGTATATTTATCCTCTGGCACGGGAACCTTCAGCGCATTAAACTACAAACACAAGGGCACGGGA CAGTATATTTATCCTCTGGCACGGGAACCTTCGGCGCATTAAACTACAAACACAAGGGCACGGGA A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75040042..75040203 26863196 MeRIP-seq:(Medium) rs371625622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1864388 100303 RMVar_ID_100303 Human_SNP_ID_632734679 m1A Human chr17 + 75042231 75042231 75042231 CACCAAGCCAGCCTTGGCCACATTGGCCTTGTAGTAAGCCCAGTCGATAGCTGGTGGATTCTCAG CACCAAGCCAGCCTTGGCCACATTGGCCTTGTGGTAAGCCCAGTCGATAGCTGGTGGATTCTCAG A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75042176..75042300 32194978 MeRIP-seq:(Medium) rs1195558787 Functional Loss SNV dbSNP153 33..33 33 - - - 100304 RMVar_ID_100304 Human_SNP_ID_632734798 m1A Human chr17 - 75042651 75042651 75042651 GTTTTTATTTGACTTATTTTTCAGGATCCCAAAATGGCTGGGCGAAAACTTGCTCTAAAAACCAT GTTTTTATTTGACTTATTTTTCAGGATCCCAAGATGGCTGGGCGAAAACTTGCTCTAAAAACCAT T C ATP5PD Ensembl:ENSG00000167863 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75042601..75042675 26863196 MeRIP-seq:(Medium) rs9660 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_499294,Human_RBP_ID_904738,Human_RBP_ID_4465651,Human_RBP_ID_9376804,Human_RBP_ID_18708215,Human_RBP_ID_22445745,Human_RBP_ID_26332341,Human_RBP_ID_27259372 Human_Splice_Rec_1864438,Human_Splice_Rec_1864448,Human_Splice_Rec_1864456 GWAS_ID_13183,GWAS_ID_13184 RMVar_hsa_circ_186950,RMVar_hsa_circ_108909,RMVar_hsa_circ_121601,RMVar_hsa_circ_186953,RMVar_hsa_circ_92695,RMVar_hsa_circ_370710,RMVar_hsa_circ_186952,RMVar_hsa_circ_279733,RMVar_hsa_circ_186954,RMVar_hsa_circ_186956 100305 RMVar_ID_100305 Human_SNP_ID_632736293 m1A Human chr17 + 75047487 75047487 75047487 GGCGCGGCCCGCTGGGTCAGGCTGAACGTGGGAGGCACCTACTTCGTGACCACCAGACAGACCTT GGCGCGGCCCGCTGGGTCAGGCTGAACGTGGGCGGCACCTACTTCGTGACCACCAGACAGACCTT A C KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75047343..75047552 26863196 MeRIP-seq:(Medium) rs1006804895 Functional Loss SNV dbSNP153 33..33 33 - - - 100306 RMVar_ID_100306 Human_SNP_ID_632736294 m1A Human chr17 + 75047487 75047487 75047487 GGCGCGGCCCGCTGGGTCAGGCTGAACGTGGGAGGCACCTACTTCGTGACCACCAGACAGACCTT GGCGCGGCCCGCTGGGTCAGGCTGAACGTGGGGGGCACCTACTTCGTGACCACCAGACAGACCTT A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75047343..75047552 26863196 MeRIP-seq:(Medium) rs1006804895 Functional Loss SNV dbSNP153 33..33 33 - - - 100307 RMVar_ID_100307 Human_SNP_ID_632747538 m1A Human chr17 - 75088046 75088038 75088046 GTCCGAGGCAGTGGGGCCCGGGGGGCCCGCTCACCCGCTCGCACGGGCCTGGCGGAGAGGTGGCT GTCCGAGGCAGTGGGGCCCGGGGGGCCCGCTC________GCACGGGCCTGGCGGAGAGGTGGCT CGAGCGGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75088014..75088085 26863196 MeRIP-seq:(Medium) rs975600749 Functional Loss DEL dbSNP153 33..40 33 - - - 100308 RMVar_ID_100308 Human_SNP_ID_632753887 m1A Human chr17 + 75110131 75110131 75110131 CGTCCCATCTCCCATATCCCATTTCCAGCTGCAAATTACTGCAGAATCTGAACCCAGGAAAGAAA CGTCCCATCTCCCATATCCCATTTCCAGCTGCGAATTACTGCAGAATCTGAACCCAGGAAAGAAA A G ARMC7 Ensembl:ENSG00000125449 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:75110030..75110156 26863410 MeRIP-seq:(Medium) rs575608536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499365,Human_RBP_ID_4465656,Human_RBP_ID_5466975 100309 RMVar_ID_100309 Human_SNP_ID_632759831 m1A Human chr17 - 75130826 75130826 75130826 GTGGAGCAGCACCTGGGGCCCCAGTTCGTAGAACGAATTATCCTGACAAGGGACAAGACGGTGGT GTGGAGCAGCACCTGGGGCCCCAGTTCGTAGAGCGAATTATCCTGACAAGGGACAAGACGGTGGT T C NT5C Ensembl:ENSG00000125458 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75130801..75130825 26863196 MeRIP-seq:(Medium) rs1007787173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1541692,Human_RBP_ID_1868828,Human_RBP_ID_13157516,Human_RBP_ID_24559287 Human_Splice_Rec_1864568,Human_Splice_Rec_1864569,Human_Splice_Rec_1864576,Human_Splice_Rec_1864577,Human_Splice_Rec_1864584,Human_Splice_Rec_1864585,Human_Splice_Rec_1864588,Human_Splice_Rec_1864589,Human_Splice_Rec_1864600,Human_Splice_Rec_1864601,Human_Splice_Rec_1864608,Human_Splice_Rec_1864609,Human_Splice_Rec_1864611,Human_Splice_Rec_1864618,Human_Splice_Rec_1864619,Human_Splice_Rec_1864624,Human_Splice_Rec_1864625,Human_Splice_Rec_1864630,Human_Splice_Rec_1864634,Human_Splice_Rec_1864635,Human_Splice_Rec_1864642 RMVar_hsa_circ_80790,RMVar_hsa_circ_116495,RMVar_hsa_circ_186961,RMVar_hsa_circ_186962 100310 RMVar_ID_100310 Human_SNP_ID_632759966 m1A Human chr17 - 75131100 75131098 75131101 CGGCGGTAACCGCGTCCTTCTCCGCAGCACGCAGGTCTTCATCTGCACCAGCCCCCTGCTGAAGT CGGCGGTAACCGCGTCCTTCTCCGCAGCACG___GTCTTCATCTGCACCAGCCCCCTGCTGAAGT CCTG C NT5C Ensembl:ENSG00000125458 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75131051..75131125 32194978 MeRIP-seq:(Medium) rs1555649384 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5364776,Human_RBP_ID_19083790,Human_RBP_ID_22656738,Human_RBP_ID_25337325 Human_Splice_Rec_1864566,Human_Splice_Rec_1864567,Human_Splice_Rec_1864574,Human_Splice_Rec_1864575,Human_Splice_Rec_1864594,Human_Splice_Rec_1864595,Human_Splice_Rec_1864598,Human_Splice_Rec_1864604,Human_Splice_Rec_1864605,Human_Splice_Rec_1864607,Human_Splice_Rec_1864616,Human_Splice_Rec_1864617,Human_Splice_Rec_1864628,Human_Splice_Rec_1864633,Human_Splice_Rec_1864640 RMVar_hsa_circ_80790,RMVar_hsa_circ_116495,RMVar_hsa_circ_186961,RMVar_hsa_circ_186962 100311 RMVar_ID_100311 Human_SNP_ID_632759968 m1A Human chr17 - 75131100 75131100 75131100 CGGCGGTAACCGCGTCCTTCTCCGCAGCACGCAGGTCTTCATCTGCACCAGCCCCCTGCTGAAGT CGGCGGTAACCGCGTCCTTCTCCGCAGCACGCGGGTCTTCATCTGCACCAGCCCCCTGCTGAAGT T C NT5C Ensembl:ENSG00000125458 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75131051..75131125 32194978 MeRIP-seq:(Medium) rs781358254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5364776,Human_RBP_ID_19083790,Human_RBP_ID_22656738,Human_RBP_ID_25337325 Human_Splice_Rec_1864566,Human_Splice_Rec_1864567,Human_Splice_Rec_1864574,Human_Splice_Rec_1864575,Human_Splice_Rec_1864594,Human_Splice_Rec_1864595,Human_Splice_Rec_1864598,Human_Splice_Rec_1864604,Human_Splice_Rec_1864605,Human_Splice_Rec_1864607,Human_Splice_Rec_1864616,Human_Splice_Rec_1864617,Human_Splice_Rec_1864628,Human_Splice_Rec_1864633,Human_Splice_Rec_1864640 RMVar_hsa_circ_80790,RMVar_hsa_circ_116495,RMVar_hsa_circ_186961,RMVar_hsa_circ_186962 100312 RMVar_ID_100312 Human_SNP_ID_632760082 m1A Human chr17 - 75131258 75131258 75131258 GTCTTTCAGGATAAAGTGGCCAGTGTGTACGAAGCCCCGGGCTTTTTCCTGGACCTGGAGCCCAT GTCTTTCAGGATAAAGTGGCCAGTGTGTACGACGCCCCGGGCTTTTTCCTGGACCTGGAGCCCAT T G NT5C Ensembl:ENSG00000125458 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75131207..75131411 26863196 MeRIP-seq:(Medium) rs1338845422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1010395,Human_RBP_ID_5237929,Human_RBP_ID_22500370,Human_RBP_ID_25337326,Human_RBP_ID_26970724 Human_Splice_Rec_1864565,Human_Splice_Rec_1864572,Human_Splice_Rec_1864573,Human_Splice_Rec_1864580,Human_Splice_Rec_1864581,Human_Splice_Rec_1864592,Human_Splice_Rec_1864593,Human_Splice_Rec_1864597,Human_Splice_Rec_1864603,Human_Splice_Rec_1864614,Human_Splice_Rec_1864615,Human_Splice_Rec_1864622,Human_Splice_Rec_1864627,Human_Splice_Rec_1864632,Human_Splice_Rec_1864638,Human_Splice_Rec_1864639 RMVar_hsa_circ_80790,RMVar_hsa_circ_116495,RMVar_hsa_circ_186961,RMVar_hsa_circ_186962,RMVar_hsa_circ_186963,RMVar_hsa_circ_322894 100313 RMVar_ID_100313 Human_SNP_ID_632760240 m1A Human chr17 - 75131588 75131588 75131588 TTCCCTGAGGAGCCGCACGTGCCGCTGGAGCAACGCCGCGGCTTCCTGGCCCGCGAGCAGTACCG TTCCCTGAGGAGCCGCACGTGCCGCTGGAGCAGCGCCGCGGCTTCCTGGCCCGCGAGCAGTACCG T C NT5C Ensembl:ENSG00000125458 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4788867 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4465657,Human_RBP_ID_9376806,Human_RBP_ID_18992112,Human_RBP_ID_22959490 Human_Splice_Rec_1864571,Human_Splice_Rec_1864579,Human_Splice_Rec_1864591,Human_Splice_Rec_1864613,Human_Splice_Rec_1864621,Human_Splice_Rec_1864631,Human_Splice_Rec_1864637 RMVar_hsa_circ_116495,RMVar_hsa_circ_186962 100314 RMVar_ID_100314 Human_SNP_ID_632760328 m1A Human chr17 + 75131722 75131722 75131722 GCGCACGCTCCGCGCCATCGCCGCCGGGCCGGAGCTGCGAGCTCTCGGGGTCTGGGGGGCGCGGG GCGCACGCTCCGCGCCATCGCCGCCGGGCCGGGGCTGCGAGCTCTCGGGGTCTGGGGGGCGCGGG A G AC022211.5 Ensembl:ENSG00000279035 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75131547..75131775 26863196 MeRIP-seq:(Medium) rs920053619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17900546 100315 RMVar_ID_100315 Human_SNP_ID_632761723 m1A Human chr17 - 75136207 75136207 75136207 ACAGACTTGCCAGGCAGCCTGGGGCAGAGTGAAGAGAAGCCCGTGCCTGCTGCGCCTGTGCCCAG ACAGACTTGCCAGGCAGCCTGGGGCAGAGTGAGGAGAAGCCCGTGCCTGCTGCGCCTGTGCCCAG T C JPT1 Ensembl:ENSG00000189159 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75136026..75136275 32194978 MeRIP-seq:(Medium) rs780975012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237113,Human_RBP_ID_499417,Human_RBP_ID_1541716,Human_RBP_ID_4450055,Human_RBP_ID_5114843,Human_RBP_ID_6642517,Human_RBP_ID_8462728,Human_RBP_ID_13240506,Human_RBP_ID_17654315,Human_RBP_ID_22443153,Human_RBP_ID_22761676,Human_RBP_ID_23748572 Human_Splice_Rec_1864650,Human_Splice_Rec_1864658,Human_Splice_Rec_1864666,Human_Splice_Rec_1864676,Human_Splice_Rec_1864682,Human_Splice_Rec_1864690,Human_Splice_Rec_1864692,Human_Splice_Rec_1864700,Human_Splice_Rec_1864708,Human_Splice_Rec_1864716 Human_miRNA_ID_2223530,Human_miRNA_ID_2223531,Human_miRNA_ID_2486601,Human_miRNA_ID_2486602,Human_miRNA_ID_2491738,Human_miRNA_ID_2491739,Human_miRNA_ID_3074966,Human_miRNA_ID_3074967,Human_miRNA_ID_3118817,Human_miRNA_ID_3118818 RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_98521,RMVar_hsa_circ_186966,RMVar_hsa_circ_186964 100316 RMVar_ID_100316 Human_SNP_ID_632766934 m1A Human chr17 - 75154464 75154464 75154464 GCGGTGGTCGGCTGTTGGGTGTGGAGTTTCCCAGCGCCCCTCGGGTCCGACCCTTTGAGCGTTCT GCGGTGGTCGGCTGTTGGGTGTGGAGTTTCCCGGCGCCCCTCGGGTCCGACCCTTTGAGCGTTCT T C JPT1 Ensembl:ENSG00000189159 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:75154291..75154525;chr17:75154287..75154525;chr17:75154296..75154525 26863196 MeRIP-seq:(Medium) rs191312728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766647,Human_RBP_ID_822362,Human_RBP_ID_1541755,Human_RBP_ID_4450070,Human_RBP_ID_5319234,Human_RBP_ID_6642663,Human_RBP_ID_8462761,Human_RBP_ID_9326814,Human_RBP_ID_18419725,Human_RBP_ID_26970753 Human_miRNA_ID_2391062,Human_miRNA_ID_2592307 RMVar_hsa_circ_111684,RMVar_hsa_circ_186964 100317 RMVar_ID_100317 Human_SNP_ID_632775714 m1A Human chr17 - 75182745 75182745 75182745 GTGGGGGTCATGGCGCGGGCCGGGGTCCGGCCAGAGCCCGCCGCTGGCTCCCAGCGCTTTCCCGG GTGGGGGTCATGGCGCGGGCCGGGGTCCGGCCGGAGCCCGCCGCTGGCTCCCAGCGCTTTCCCGG T C SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:75182740..75182896 26863196 MeRIP-seq:(Medium) rs1014211137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_900667,Human_RBP_ID_5364785,Human_RBP_ID_13158898,Human_RBP_ID_19083797,Human_RBP_ID_22357388 100318 RMVar_ID_100318 Human_SNP_ID_632775745 m1A Human chr17 - 75182821 75182821 75182821 GGAGACTCCGGCGCTCGCCATGGCCGACGAAAAGCCCAAGGTGAGCTCGCCGCCGGCCCCTTCGC GGAGACTCCGGCGCTCGCCATGGCCGACGAAATGCCCAAGGTGAGCTCGCCGCCGGCCCCTTCGC T A SUMO2 Ensembl:ENSG00000188612 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1204157058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499468,Human_RBP_ID_8462778,Human_RBP_ID_9326815,Human_RBP_ID_19079869,Human_RBP_ID_22443894,Human_RBP_ID_26333809,Human_RBP_ID_26970767 Human_Splice_Rec_1864727,Human_Splice_Rec_1864733 100319 RMVar_ID_100319 Human_SNP_ID_632775786 m1A Human chr17 + 75182906 75182906 75182906 GAGGTACCAGGTCCGCACCAAACGAGCACACAAGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG GAGGTACCAGGTCCGCACCAAACGAGCACACAGGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:75182769..75182946 26863410 MeRIP-seq:(Medium) rs1241157161 Functional Loss SNV dbSNP153 33..33 33 - - - 100320 RMVar_ID_100320 Human_SNP_ID_632775787 m1A Human chr17 + 75182906 75182906 75182906 GAGGTACCAGGTCCGCACCAAACGAGCACACAAGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG GAGGTACCAGGTCCGCACCAAACGAGCACACATGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:75182769..75182946 26863410 MeRIP-seq:(Medium) rs1241157161 Functional Loss SNV dbSNP153 33..33 33 - - - 100321 RMVar_ID_100321 Human_SNP_ID_632782801 m1A Human chr17 - 75205748 75205748 75205748 CGCCATCGAGCTCCTCCATAGCGCCGAACCCCAGGCTCCTAGAAGTCGCTCGGACGCCAATGCTT CGCCATCGAGCTCCTCCATAGCGCCGAACCCCGGGCTCCTAGAAGTCGCTCGGACGCCAATGCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:75205701..75205835;chr17:75205552..75205824 26863196 MeRIP-seq:(Medium) rs1158296472 Functional Loss SNV dbSNP153 33..33 33 - - - 100322 RMVar_ID_100322 Human_SNP_ID_632786393 m1A Human chr17 + 75218236 75218236 75218236 TCTCCTTGACTGGGTCCGGCTCCATGTGTGCGAGGTGGACAGTTTGTCGGCAGATGTTCTGGGCA TCTCCTTGACTGGGTCCGGCTCCATGTGTGCGGGGTGGACAGTTTGTCGGCAGATGTTCTGGGCA A G NUP85 Ensembl:ENSG00000125450 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75215800..75218235 32194978 MeRIP-seq:(Medium) rs745464633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_278837,Human_RBP_ID_1184197,Human_RBP_ID_1541804,Human_RBP_ID_1868901,Human_RBP_ID_8462796,Human_RBP_ID_9326816,Human_RBP_ID_13159433,Human_RBP_ID_18708358,Human_RBP_ID_18992125,Human_RBP_ID_23748760 Human_Splice_Rec_1864764,Human_Splice_Rec_1864765,Human_Splice_Rec_1864800,Human_Splice_Rec_1864801,Human_Splice_Rec_1864822,Human_Splice_Rec_1864823,Human_Splice_Rec_1864856,Human_Splice_Rec_1864857,Human_Splice_Rec_1864902,Human_Splice_Rec_1864903,Human_Splice_Rec_1864958,Human_Splice_Rec_1864959,Human_Splice_Rec_1864971,Human_Splice_Rec_1864979 RMVar_hsa_circ_37624,RMVar_hsa_circ_369057,RMVar_hsa_circ_330371,RMVar_hsa_circ_274370,RMVar_hsa_circ_87064,RMVar_hsa_circ_83094,RMVar_hsa_circ_186975,RMVar_hsa_circ_186976,RMVar_hsa_circ_363756,RMVar_hsa_circ_300037,RMVar_hsa_circ_357593,RMVar_hsa_circ_112245,RMVar_hsa_circ_93763,RMVar_hsa_circ_186977,RMVar_hsa_circ_186979,RMVar_hsa_circ_186978,RMVar_hsa_circ_118140,RMVar_hsa_circ_315588,RMVar_hsa_circ_24701,RMVar_hsa_circ_186981,RMVar_hsa_circ_186982,RMVar_hsa_circ_186983,RMVar_hsa_circ_310237,RMVar_hsa_circ_186985 100323 RMVar_ID_100323 Human_SNP_ID_632793392 m1A Human chr17 + 75239983 75239983 75239983 ACACTGGCTGGGACCACAGGAGCTGGGAAGGGAGGCGGCAGTGGAGCTTGGGAGCTGCTTGAGGA ACACTGGCTGGGACCACAGGAGCTGGGAAGGGGGGCGGCAGTGGAGCTTGGGAGCTGCTTGAGGA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75239898..75240053;chr17:75239932..75240092 26863196 MeRIP-seq:(Medium) rs1352790559 Functional Loss SNV dbSNP153 33..33 33 - - - 100324 RMVar_ID_100324 Human_SNP_ID_632793398 m1A Human chr17 - 75239992 75239992 75239992 TCAGCCCCCTCCTCAAGCAGCTCCCAAGCTCCACTGCCGCCTCCCTTCCCAGCTCCTGTGGTCCC TCAGCCCCCTCCTCAAGCAGCTCCCAAGCTCCGCTGCCGCCTCCCTTCCCAGCTCCTGTGGTCCC T C GGA3 Ensembl:ENSG00000125447 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75239943..75240084 26863196 MeRIP-seq:(Medium) rs1269879560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130900,Human_RBP_ID_3537058,Human_RBP_ID_3951013,Human_RBP_ID_18942104,Human_RBP_ID_26970878,Human_RBP_ID_27456835 Human_miRNA_ID_233522,Human_miRNA_ID_1365306,Human_miRNA_ID_1369986,Human_miRNA_ID_2030414,Human_miRNA_ID_2458228,Human_miRNA_ID_2463151,Human_miRNA_ID_2635792,Human_miRNA_ID_2638479,Human_miRNA_ID_2690875,Human_miRNA_ID_2694181 RMVar_hsa_circ_4347,RMVar_hsa_circ_105507,RMVar_hsa_circ_372958,RMVar_hsa_circ_186998,RMVar_hsa_circ_326100,RMVar_hsa_circ_121786,RMVar_hsa_circ_187001,RMVar_hsa_circ_92224,RMVar_hsa_circ_187002,RMVar_hsa_circ_187003 100325 RMVar_ID_100325 Human_SNP_ID_632793860 m1A Human chr17 + 75240946 75240945 75240947 CTGAGGCCTGGGGTGGTGGAGGGAGGATTGGGATGCCTGAGGAGGGTGGAGTAGGTGCTGGGGCC CTGAGGCCTGGGGTGGTGGAGGGAGGATTGGG__GCCTGAGGAGGGTGGAGTAGGTGCTGGGGCC GAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75240899..75241020 26863196 MeRIP-seq:(Medium) rs1338334342 Functional Loss DEL dbSNP153 33..34 33 - - - 100326 RMVar_ID_100326 Human_SNP_ID_632797790 m1A Human chr17 - 75253716 75253716 75253716 TTCTTACCCTCCAGAAAAGCAGGAAAGGGGTCAGGGTGTGGAAATAAGGGATTGGGGCACACAGA TTCTTACCCTCCAGAAAAGCAGGAAAGGGGTCGGGGTGTGGAAATAAGGGATTGGGGCACACAGA T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75253713..75253899 26863196 MeRIP-seq:(Medium) rs201074686 Functional Loss SNV dbSNP153 33..33 33 - - - 100327 RMVar_ID_100327 Human_SNP_ID_632797802 m1A Human chr17 - 75253752 75253752 75253752 GAGAGAGTAGAGACACGGAGGGAAGGGGTTCGAGGGTTCTTACCCTCCAGAAAAGCAGGAAAGGG GAGAGAGTAGAGACACGGAGGGAAGGGGTTCGGGGGTTCTTACCCTCCAGAAAAGCAGGAAAGGG T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75253750..75253924 26863196 MeRIP-seq:(Medium) rs1174524812 Functional Loss SNV dbSNP153 33..33 33 - - - 100328 RMVar_ID_100328 Human_SNP_ID_632798570 m1A Human chr17 - 75256204 75256204 75256204 TAAAGCAGCGGCAGCCACTGCAAGCAGACATGAGGGCTAGGCTAAAACAGTAAGGTCAAGTTGTT TAAAGCAGCGGCAGCCACTGCAAGCAGACATGGGGGCTAGGCTAAAACAGTAAGGTCAAGTTGTT T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75256202..75256441 26863196 MeRIP-seq:(Medium) rs1283755209 Functional Loss SNV dbSNP153 33..33 33 - - - 100329 RMVar_ID_100329 Human_SNP_ID_632800407 m1A Human chr17 - 75261937 75261937 75261937 GACAGCCCGCCGCACGCCCAACGCCAGGCCCGACCATCCTCGGGCAACCTTCACTGCGGGGGCAG GACAGCCCGCCGCACGCCCAACGCCAGGCCCGGCCATCCTCGGGCAACCTTCACTGCGGGGGCAG T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75261876..75262170 26863196 MeRIP-seq:(Medium) rs1406020989 Functional Loss SNV dbSNP153 33..33 33 - - - 100330 RMVar_ID_100330 Human_SNP_ID_632800437 m1A Human chr17 - 75261978 75261978 75261978 CCCCGCCGCTGCTCGCCACCCTCTCACCCTGGAAGCTGCAAGACAGCCCGCCGCACGCCCAACGC CCCCGCCGCTGCTCGCCACCCTCTCACCCTGGTAGCTGCAAGACAGCCCGCCGCACGCCCAACGC T A GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75261826..75262021 32194978 MeRIP-seq:(Medium) rs1314173730 Functional Loss SNV dbSNP153 33..33 33 - - - 100331 RMVar_ID_100331 Human_SNP_ID_632800438 m1A Human chr17 - 75261978 75261978 75261978 CCCCGCCGCTGCTCGCCACCCTCTCACCCTGGAAGCTGCAAGACAGCCCGCCGCACGCCCAACGC CCCCGCCGCTGCTCGCCACCCTCTCACCCTGGGAGCTGCAAGACAGCCCGCCGCACGCCCAACGC T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75261826..75262021 32194978 MeRIP-seq:(Medium) rs1314173730 Functional Loss SNV dbSNP153 33..33 33 - - - 100332 RMVar_ID_100332 Human_SNP_ID_632800699 m1A Human chr17 - 75262566 75262566 75262566 TCCTCCTCAGTTAGCTCCTCCACTGGCTTGCGATAATATTCCTTGTCAATCAAGGGATCCTTGAA TCCTCCTCAGTTAGCTCCTCCACTGGCTTGCGGTAATATTCCTTGTCAATCAAGGGATCCTTGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:75262462..75262652;chr17:75262476..75262633;chr17:75262501..75262650;chr17:75262468..75262600 26863196 MeRIP-seq:(Medium) rs776249725 Functional Loss SNV dbSNP153 33..33 33 - - - 100333 RMVar_ID_100333 Human_SNP_ID_632800995 m1A Human chr17 - 75263467 75263467 75263467 AACGGCCTCCCTTGAGGATGGGTACCAGCCCAATCATAGGCTCACAGTTTTTCAGTGCTTGATGG AACGGCCTCCCTTGAGGATGGGTACCAGCCCAGTCATAGGCTCACAGTTTTTCAGTGCTTGATGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75263417..75263548 26863196 MeRIP-seq:(Medium) rs760241093 Functional Loss SNV dbSNP153 33..33 33 - - - 100334 RMVar_ID_100334 Human_SNP_ID_632801947 m1A Human chr17 + 75266750 75266750 75266750 GAGGAAGCCCTGATCTGGAGGCCTAGTCGGAGACTTCGCTGTAGTAATACTTGTGGGCAGCTGGC GAGGAAGCCCTGATCTGGAGGCCTAGTCGGAGGCTTCGCTGTAGTAATACTTGTGGGCAGCTGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75266702..75266782 26863196 MeRIP-seq:(Medium) rs138799236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8462900 100335 RMVar_ID_100335 Human_SNP_ID_632803755 m1A Human chr17 - 75272059 75272059 75272059 GGTCCAGGCTGCGGCGGGGGCCACGAGGATGCAGCTGCCTGAATGCATTTTTTATGAAATTCCGT GGTCCAGGCTGCGGCGGGGGCCACGAGGATGCGGCTGCCTGAATGCATTTTTTATGAAATTCCGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75272041..75272149 26863196 MeRIP-seq:(Medium) rs1390796352 Functional Loss SNV dbSNP153 33..33 33 - - - 100336 RMVar_ID_100336 Human_SNP_ID_632804136 m1A Human chr17 + 75273115 75273115 75273115 TGCACTCAAGCAGCAGCCCCATCCAGACCAGGAGTGTGTTCTGTTCTCCTGGCAGGCAGGGCTGA TGCACTCAAGCAGCAGCCCCATCCAGACCAGGGGTGTGTTCTGTTCTCCTGGCAGGCAGGGCTGA A G AC022211.3 Ensembl:ENSG00000263843 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75273029..75273129 32194978 MeRIP-seq:(Medium) rs1258716604 Functional Loss SNV dbSNP153 33..33 33 - - - 100337 RMVar_ID_100337 Human_SNP_ID_632807977 m1A Human chr17 - 75286745 75286745 75286745 GCCAGAGGCAGGGATGGTTGGCTATGACCCCAAACCAGATGGCAGGAATAACACCAAGTTCCAGG GCCAGAGGCAGGGATGGTTGGCTATGACCCCAGACCAGATGGCAGGAATAACACCAAGTTCCAGG T C SLC25A19 Ensembl:ENSG00000125454 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75286698..75286857 26863196 MeRIP-seq:(Medium) rs762770947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466784 Human_Splice_Rec_1865632,Human_Splice_Rec_1865646,Human_Splice_Rec_1865668,Human_Splice_Rec_1865684,Human_Splice_Rec_1865698,Human_Splice_Rec_1865712,Human_Splice_Rec_1865728,Human_Splice_Rec_1865736,Human_Splice_Rec_1865744,Human_Splice_Rec_1865752,Human_Splice_Rec_1865756 Clinvar_Rec_615 RMVar_hsa_circ_352087,RMVar_hsa_circ_300175,RMVar_hsa_circ_278505,RMVar_hsa_circ_367193 100338 RMVar_ID_100338 Human_SNP_ID_632837073 m1A Human chr17 + 75393753 75393753 75393753 CTCTTCTGGGACTCGCTCCGGCACTCTGGGACACACAATGCCACCCTGAAGCAGGAGAGGGACGA CTCTTCTGGGACTCGCTCCGGCACTCTGGGACTCACAATGCCACCCTGAAGCAGGAGAGGGACGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:75393651..75393846;chr17:75393654..75393845 26863196 MeRIP-seq:(Medium) rs1417437621 Functional Loss SNV dbSNP153 33..33 33 - - - 100339 RMVar_ID_100339 Human_SNP_ID_632840252 m1A Human chr17 - 75405514 75405514 75405514 GCCGCTCGCAGCGTTGTGGAGGGGCGGGCCGGACGCTGAGCGGAGCAGCTGCGCCACGGTGAGTA GCCGCTCGCAGCGTTGTGGAGGGGCGGGCCGGGCGCTGAGCGGAGCAGCTGCGCCACGGTGAGTA T C GRB2 Ensembl:ENSG00000177885 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75405501..75405525 32194978 MeRIP-seq:(Medium) rs982834508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238198,Human_RBP_ID_4464781,Human_RBP_ID_5237932,Human_RBP_ID_5420489,Human_RBP_ID_5466990,Human_RBP_ID_8463006,Human_RBP_ID_8824949,Human_RBP_ID_8941848,Human_RBP_ID_9289358,Human_RBP_ID_9327433,Human_RBP_ID_9353451,Human_RBP_ID_22061633,Human_RBP_ID_22443896,Human_RBP_ID_24552523 Human_Splice_Rec_1865787,Human_Splice_Rec_1865797,Human_Splice_Rec_1865805,Human_Splice_Rec_1865839 100340 RMVar_ID_100340 Human_SNP_ID_632840258 m1A Human chr17 + 75405541 75405541 75405541 CAGCGTCCGGCCCGCCCCTCCACAACGCTGCGAGCGGCCGGCGACCCCAAGGCTGCTCTGCGAGG CAGCGTCCGGCCCGCCCCTCCACAACGCTGCGCGCGGCCGGCGACCCCAAGGCTGCTCTGCGAGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr17:75405388..75405650;chr17:75405439..75405746 26863196 MeRIP-seq:(Medium) rs991212057 Functional Loss SNV dbSNP153 33..33 33 - - - 100341 RMVar_ID_100341 Human_SNP_ID_632840259 m1A Human chr17 + 75405541 75405541 75405541 CAGCGTCCGGCCCGCCCCTCCACAACGCTGCGAGCGGCCGGCGACCCCAAGGCTGCTCTGCGAGG CAGCGTCCGGCCCGCCCCTCCACAACGCTGCGTGCGGCCGGCGACCCCAAGGCTGCTCTGCGAGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr17:75405388..75405650;chr17:75405439..75405746 26863196 MeRIP-seq:(Medium) rs991212057 Functional Loss SNV dbSNP153 33..33 33 - - - 100342 RMVar_ID_100342 Human_SNP_ID_632840267 m1A Human chr17 - 75405567 75405567 75405567 GTGACGGCGGCGGGAGCAAGCGCTGCCCTCGCAGAGCAGCCTTGGGGTCGCCGGCCGCTCGCAGC GTGACGGCGGCGGGAGCAAGCGCTGCCCTCGCCGAGCAGCCTTGGGGTCGCCGGCCGCTCGCAGC T G GRB2 Ensembl:ENSG00000177885 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75405391..75405675 26863196 MeRIP-seq:(Medium) rs1404513926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499762,Human_RBP_ID_4464781,Human_RBP_ID_5318582,Human_RBP_ID_8825715,Human_RBP_ID_8941848,Human_RBP_ID_9289359,Human_RBP_ID_9327433,Human_RBP_ID_9353451 Human_Splice_Rec_1865787,Human_Splice_Rec_1865797,Human_Splice_Rec_1865805,Human_Splice_Rec_1865839 100343 RMVar_ID_100343 Human_SNP_ID_632857853 m1A Human chr17 + 75471892 75471892 75471892 AGGGGTGACCACATTCATCTGGGCATGCCTGCAGTACTCTTGGCCCATGGACCTGAAGGAGAAGC AGGGGTGACCACATTCATCTGGGCATGCCTGCGGTACTCTTGGCCCATGGACCTGAAGGAGAAGC A G TMEM94 Ensembl:ENSG00000177728 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75471743..75471922 26863196 MeRIP-seq:(Medium) rs1339579488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3537192,Human_RBP_ID_3952908,Human_RBP_ID_13162444,Human_RBP_ID_18470287,Human_RBP_ID_18992162 Human_Splice_Rec_1865844,Human_Splice_Rec_1865845,Human_Splice_Rec_1865852,Human_Splice_Rec_1865853,Human_Splice_Rec_1865912,Human_Splice_Rec_1865913,Human_Splice_Rec_1865920,Human_Splice_Rec_1865921,Human_Splice_Rec_1865926,Human_Splice_Rec_1865927,Human_Splice_Rec_1865986,Human_Splice_Rec_1865987,Human_Splice_Rec_1865992,Human_Splice_Rec_1866002,Human_Splice_Rec_1866003,Human_Splice_Rec_1866048,Human_Splice_Rec_1866049,Human_Splice_Rec_1866054,Human_Splice_Rec_1866055 Human_miRNA_ID_1993935 RMVar_hsa_circ_76065,RMVar_hsa_circ_291988,RMVar_hsa_circ_187015,RMVar_hsa_circ_378011,RMVar_hsa_circ_265878,RMVar_hsa_circ_187016,RMVar_hsa_circ_187017 100344 RMVar_ID_100344 Human_SNP_ID_632861226 m1A Human chr17 - 75485944 75485944 75485944 AGCAGCCCAGCAGCAGCAGCACGGCCAGTAGCATGAGTGAGGCCCCCGGCCAGTGGAAGCAGGAG AGCAGCCCAGCAGCAGCAGCACGGCCAGTAGCGTGAGTGAGGCCCCCGGCCAGTGGAAGCAGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75485895..75486045 32194978 MeRIP-seq:(Medium) rs375551454 Functional Loss SNV dbSNP153 33..33 33 - - - 100345 RMVar_ID_100345 Human_SNP_ID_632863358 m1A Human chr17 - 75492788 75492788 75492788 GCCAGCCATCCCCTGCCATGGGGACCTGTACCAATGAGGCGGGCAAGCTCGCAGAGGCCCCAGGG GCCAGCCATCCCCTGCCATGGGGACCTGTACCGATGAGGCGGGCAAGCTCGCAGAGGCCCCAGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75492709..75492810 32194978 MeRIP-seq:(Medium) rs760440197 Functional Loss SNV dbSNP153 33..33 33 - - - 100346 RMVar_ID_100346 Human_SNP_ID_632863465 m1A Human chr17 - 75493056 75493056 75493056 TTAATGAAGAGGCTGATCATGTGGCTGAGGGGAGGCCGCCGCTTGGTGACACAGGAGAGCCGCCC TTAATGAAGAGGCTGATCATGTGGCTGAGGGGCGGCCGCCGCTTGGTGACACAGGAGAGCCGCCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75493008..75493108 32194978 MeRIP-seq:(Medium) rs1027014577 Functional Loss SNV dbSNP153 33..33 33 - - - 100347 RMVar_ID_100347 Human_SNP_ID_632866308 m1A Human chr17 - 75501923 75501923 75501923 AGCCCAGCAGCCTTCCAGCCCAAGGAGTTCCAACCCCCCTTGCTCCCAGCCCCGCCATGCAGCCT AGCCCAGCAGCCTTCCAGCCCAAGGAGTTCCAGCCCCCCTTGCTCCCAGCCCCGCCATGCAGCCT T C CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75501876..75502125 26863196 MeRIP-seq:(Medium) rs964842021 Functional Loss SNV dbSNP153 33..33 33 - - - 100348 RMVar_ID_100348 Human_SNP_ID_632866314 m1A Human chr17 - 75501939 75501939 75501939 AGCCTTCCCCAGCCCGAGCCCAGCAGCCTTCCAGCCCAAGGAGTTCCAACCCCCCTTGCTCCCAG AGCCTTCCCCAGCCCGAGCCCAGCAGCCTTCCTGCCCAAGGAGTTCCAACCCCCCTTGCTCCCAG T A CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75501889..75502238 26863196 MeRIP-seq:(Medium) rs767839500 Functional Loss SNV dbSNP153 33..33 33 - - - 100349 RMVar_ID_100349 Human_SNP_ID_632866345 m1A Human chr17 - 75501998 75501998 75501998 CGCCTGGCCCCGCTGCCCCACTGCCTTCCCCAACTCCTGGCGAGTCTCCTCCAGCTTCTAGCCTT CGCCTGGCCCCGCTGCCCCACTGCCTTCCCCATCTCCTGGCGAGTCTCCTCCAGCTTCTAGCCTT T A CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75501949..75502175 26863196 MeRIP-seq:(Medium) rs1448195025 Functional Loss SNV dbSNP153 33..33 33 - - - 100350 RMVar_ID_100350 Human_SNP_ID_632866622 m1A Human chr17 + 75502492 75502492 75502492 GCGGGGGCGGGGGGCCTTTGCGCCGGGCCCGCAGGGCAAAGGACTGGCTGCGAGGAGTCCCCCGA GCGGGGGCGGGGGGCCTTTGCGCCGGGCCCGCGGGGCAAAGGACTGGCTGCGAGGAGTCCCCCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75502441..75502663 26863196 MeRIP-seq:(Medium) rs1438751565 Functional Loss SNV dbSNP153 33..33 33 - - - 100351 RMVar_ID_100351 Human_SNP_ID_632866779 m1A Human chr17 + 75502741 75502741 75502741 GGGGAGTGGCAGGGGGCCCGGCCAAGTAGGAGAAGGCCCAGGGTGCGCCAGGAGGTGGCCCTGGG GGGGAGTGGCAGGGGGCCCGGCCAAGTAGGAGGAGGCCCAGGGTGCGCCAGGAGGTGGCCCTGGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75502597..75502833 26863196 MeRIP-seq:(Medium) rs1485251229 Functional Loss SNV dbSNP153 33..33 33 - - - 100352 RMVar_ID_100352 Human_SNP_ID_632867005 m1A Human chr17 - 75503132 75503132 75503132 GCCGGCTGGCCAAGGGTCCGGAGCTGATGGCCATCGAGGGACTGGAGAACGGAGAAGGCCCAGCT GCCGGCTGGCCAAGGGTCCGGAGCTGATGGCCGTCGAGGGACTGGAGAACGGAGAAGGCCCAGCT T C CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75502709..75503417 26863196 MeRIP-seq:(Medium) rs1388023446 Functional Loss SNV dbSNP153 33..33 33 - - - 100353 RMVar_ID_100353 Human_SNP_ID_632867786 m1A Human chr17 - 75504896 75504896 75504896 CACCCACCCCCCTGCGCCCAGGCTTCTCCCGGACACCGCAGCCTCCTGCCGAAGAACCCCCGCAC CACCCACCCCCCTGCGCCCAGGCTTCTCCCGGTCACCGCAGCCTCCTGCCGAAGAACCCCCGCAC T A CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75504849..75504982 26863196 MeRIP-seq:(Medium) rs749682853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1866329,Human_Splice_Rec_1866365 RMVar_hsa_circ_366311 100354 RMVar_ID_100354 Human_SNP_ID_632867787 m1A Human chr17 - 75504896 75504896 75504896 CACCCACCCCCCTGCGCCCAGGCTTCTCCCGGACACCGCAGCCTCCTGCCGAAGAACCCCCGCAC CACCCACCCCCCTGCGCCCAGGCTTCTCCCGGGCACCGCAGCCTCCTGCCGAAGAACCCCCGCAC T C CASKIN2 Ensembl:ENSG00000177303 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75504849..75504982 26863196 MeRIP-seq:(Medium) rs749682853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1866329,Human_Splice_Rec_1866365 RMVar_hsa_circ_366311 100355 RMVar_ID_100355 Human_SNP_ID_632867799 m1A Human chr17 + 75504916 75504916 75504916 GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCAGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCCGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75504871..75504968 26863196 MeRIP-seq:(Medium) rs760588063 Functional Loss SNV dbSNP153 33..33 33 - - - 100356 RMVar_ID_100356 Human_SNP_ID_632867800 m1A Human chr17 + 75504916 75504916 75504916 GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCAGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCGGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75504871..75504968 26863196 MeRIP-seq:(Medium) rs760588063 Functional Loss SNV dbSNP153 33..33 33 - - - 100357 RMVar_ID_100357 Human_SNP_ID_632870708 m1A Human chr17 + 75515457 75515457 75515457 CGGCTGGCCCTGCTCGGTCCCTGGCACTCAGGACGGTGGCTCCCACTCCCCCCTGCCCCCCTTTC CGGCTGGCCCTGCTCGGTCCCTGGCACTCAGGTCGGTGGCTCCCACTCCCCCCTGCCCCCCTTTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75515325..75515510 26863196 MeRIP-seq:(Medium) rs1390992570 Functional Loss SNV dbSNP153 33..33 33 - - - 100358 RMVar_ID_100358 Human_SNP_ID_632872903 m1A Human chr17 + 75521788 75521788 75521788 TCTGGCAGCCTCCAGCCCACCTCCCTGCAGCCAGCCCAGCCAATGCCCAGAGGAGAAACCCCAGG TCTGGCAGCCTCCAGCCCACCTCCCTGCAGCCGGCCCAGCCAATGCCCAGAGGAGAAACCCCAGG A G TSEN54 Ensembl:ENSG00000182173 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75521737..75521981 26863196 MeRIP-seq:(Medium) rs200904080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499856,Human_RBP_ID_900724,Human_RBP_ID_17900791 Human_Splice_Rec_1866442,Human_Splice_Rec_1866486,Human_Splice_Rec_1866496 Human_miRNA_ID_794143,Human_miRNA_ID_935711,Human_miRNA_ID_1158036,Human_miRNA_ID_2333065,Human_miRNA_ID_2435106,Human_miRNA_ID_2555008,Human_miRNA_ID_2966147 RMVar_hsa_circ_116486,RMVar_hsa_circ_187042 100359 RMVar_ID_100359 Human_SNP_ID_632872987 m1A Human chr17 + 75521928 75521928 75521928 GGGAGGGGGTGGGGTGCAGCTGGGAGAGTGGCAGAGCCGAGAACGGAGTCACGGGAGCCGGTAAG GGGAGGGGGTGGGGTGCAGCTGGGAGAGTGGCGGAGCCGAGAACGGAGTCACGGGAGCCGGTAAG A G TSEN54 Ensembl:ENSG00000182173 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75521877..75521992 26863196 MeRIP-seq:(Medium) rs1452630857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766422,Human_RBP_ID_822718,Human_RBP_ID_5367806,Human_RBP_ID_18989152,Human_RBP_ID_21974532 Human_miRNA_ID_2396105,Human_miRNA_ID_3069982 RMVar_hsa_circ_116486,RMVar_hsa_circ_187042 100360 RMVar_ID_100360 Human_SNP_ID_632873217 m1A Human chr17 + 75522226 75522226 75522226 GGTGCAGCGGTGCTCCAGCTGGCGGGAGTACAAGGAGCTGCTGCAGCGGCGGCAGGTGCAGAGGA GGTGCAGCGGTGCTCCAGCTGGCGGGAGTACAGGGAGCTGCTGCAGCGGCGGCAGGTGCAGAGGA A G TSEN54 Ensembl:ENSG00000182173 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:75522141..75522242 26863410 MeRIP-seq:(Medium) rs772853205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235457,Human_RBP_ID_822842,Human_RBP_ID_900725,Human_RBP_ID_18992208 RMVar_hsa_circ_116486,RMVar_hsa_circ_187042 100361 RMVar_ID_100361 Human_SNP_ID_632873327 m1A Human chr17 + 75522465 75522465 75522465 AGGAAGATGTGGGAGGAGGGAGTGGACCCACAAGCACGGTCAGTTCTCCGGCGGCTGCAGCAGGG AGGAAGATGTGGGAGGAGGGAGTGGACCCACAGGCACGGTCAGTTCTCCGGCGGCTGCAGCAGGG A G TSEN54 Ensembl:ENSG00000182173 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75522415..75522573 26863196 MeRIP-seq:(Medium) rs1000158460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1866501 RMVar_hsa_circ_116486,RMVar_hsa_circ_187042 100362 RMVar_ID_100362 Human_SNP_ID_632874444 m1A Human chr17 + 75525745 75525745 75525745 GGAAGGAGACGGCCGCCCAGCAGCCCGTGGGCAGGCGCGGCGGAGCGAGCGGGGCCGGCGGCGGG GGAAGGAGACGGCCGCCCAGCAGCCCGTGGGCGGGCGCGGCGGAGCGAGCGGGGCCGGCGGCGGG A G LLGL2 Ensembl:ENSG00000073350 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75525676..75525850;chr17:75525709..75525868;chr17:75525694..75532547 26863196 MeRIP-seq:(Medium) rs1440002727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420104 Human_Splice_Rec_1866523,Human_Splice_Rec_1866573,Human_Splice_Rec_1866621,Human_Splice_Rec_1866639,Human_Splice_Rec_1866659 RMVar_hsa_circ_79692,RMVar_hsa_circ_187048 100363 RMVar_ID_100363 Human_SNP_ID_632877952 m1A Human chr17 + 75538522 75538522 75538522 GTGGAGACCTCGCCTCCTCTGTTCATTCATTCATTCAACAGATAACGAGTGAGGACTCGCTGTGT GTGGAGACCTCGCCTCCTCTGTTCATTCATTCGTTCAACAGATAACGAGTGAGGACTCGCTGTGT A G LLGL2 Ensembl:ENSG00000073350 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75538519..75538612 26863196 MeRIP-seq:(Medium) rs1291201732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79692,RMVar_hsa_circ_187048 100364 RMVar_ID_100364 Human_SNP_ID_632879178 m1A Human chr17 + 75543307 75543305 75543307 CTGGCCCCGGGGTGGCAGCCTACTGGACTTGGAGAGAGAGGCCCTGCTCCACCTGTTTGGGCCGG CTGGCCCCGGGGTGGCAGCCTACTGGACTTG__GAGAGAGGCCCTGCTCCACCTGTTTGGGCCGG GGA G LLGL2 Ensembl:ENSG00000073350 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75543305..75543558 26863196 MeRIP-seq:(Medium) rs970193784 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_60473,RMVar_hsa_circ_79692,RMVar_hsa_circ_187048 100365 RMVar_ID_100365 Human_SNP_ID_632879187 m1A Human chr17 - 75543330 75543330 75543330 TGGCACTCAGGTATCGATTAGGCCCGGCCCAAACAGGTGGAGCAGGGCCTCTCTCTCCAAGTCCA TGGCACTCAGGTATCGATTAGGCCCGGCCCAAGCAGGTGGAGCAGGGCCTCTCTCTCCAAGTCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75543327..75543543 26863196 MeRIP-seq:(Medium) rs879548038 Functional Loss SNV dbSNP153 33..33 33 - - - 100366 RMVar_ID_100366 Human_SNP_ID_632879756 m1A Human chr17 + 75545616 75545616 75545616 GCCCTGCCCCTCCCCAGCCCAGGCTGTGAAGCAGGGAGGCTGCTGGTATCTGGGCCTGATCTGAC GCCCTGCCCCTCCCCAGCCCAGGCTGTGAAGCTGGGAGGCTGCTGGTATCTGGGCCTGATCTGAC A T LLGL2 Ensembl:ENSG00000073350 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75545614..75545718 26863196 MeRIP-seq:(Medium) rs1459660533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79692,RMVar_hsa_circ_187048 100367 RMVar_ID_100367 Human_SNP_ID_632879972 m1A Human chr17 - 75546468 75546468 75546468 AACGATGCTGCCGGACACTGCAGCCGCCAGCCAGACGTGGCCTTCGATTCGTGCAGGAACTCATG AACGATGCTGCCGGACACTGCAGCCGCCAGCCGGACGTGGCCTTCGATTCGTGCAGGAACTCATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75546466..75546583 26863196 MeRIP-seq:(Medium) rs116293487 Functional Loss SNV dbSNP153 33..33 33 - - - 100368 RMVar_ID_100368 Human_SNP_ID_632883795 m1A Human chr17 + 75559335 75559335 75559335 CGAGCTGCTCTACCTGGGCACCGAGAGTGGCAACGTGTTTGTGGTGCAGCTGCCAGCTTTTCGTG CGAGCTGCTCTACCTGGGCACCGAGAGTGGCAGCGTGTTTGTGGTGCAGCTGCCAGCTTTTCGTG A G LLGL2 Ensembl:ENSG00000073350 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr17:75559220..75559448;chr17:75559217..75559400;chr17:75559267..75562336 26863196,32194978 MeRIP-seq:(Medium) rs770564636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1866522,Human_Splice_Rec_1866532,Human_Splice_Rec_1866533,Human_Splice_Rec_1866582,Human_Splice_Rec_1866583,Human_Splice_Rec_1866630,Human_Splice_Rec_1866631,Human_Splice_Rec_1866650,Human_Splice_Rec_1866651,Human_Splice_Rec_1866678,Human_Splice_Rec_1866679,Human_Splice_Rec_1866738,Human_Splice_Rec_1866746,Human_Splice_Rec_1866750,Human_Splice_Rec_1866751,Human_Splice_Rec_1866789 RMVar_hsa_circ_79692,RMVar_hsa_circ_187048,RMVar_hsa_circ_187049,RMVar_hsa_circ_126648,RMVar_hsa_circ_372097,RMVar_hsa_circ_187050,RMVar_hsa_circ_187051,RMVar_hsa_circ_91017 100369 RMVar_ID_100369 Human_SNP_ID_632883805 m1A Human chr17 - 75559360 75559360 75559360 GAGCTGATGGTCCGGTCCTCCAGCGCACGAAAAGCTGGCAGCTGCACCACAAACACGTTGCCACT GAGCTGATGGTCCGGTCCTCCAGCGCACGAAAGGCTGGCAGCTGCACCACAAACACGTTGCCACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75559210..75559361 26863196 MeRIP-seq:(Medium) rs922967693 Functional Loss SNV dbSNP153 33..33 33 - - - 100370 RMVar_ID_100370 Human_SNP_ID_632885772 m1A Human chr17 + 75566288 75566288 75566288 TGAGGGAGATGAGGGCCCTGAGCAGGGGTGCCATGATCTAGCCTCTGCTCCAGAAGGATCTGTCT TGAGGGAGATGAGGGCCCTGAGCAGGGGTGCCGTGATCTAGCCTCTGCTCCAGAAGGATCTGTCT A G LLGL2 Ensembl:ENSG00000073350 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75566287..75566387 26863196 MeRIP-seq:(Medium) rs1048527266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768008,Human_RBP_ID_819731,Human_RBP_ID_3951060 100371 RMVar_ID_100371 Human_SNP_ID_632893455 m1A Human chr17 + 75589400 75589396 75589400 AGGGGACGAGGGTCGGGGCCGCGGGAAAGCGGACGAAGGGCGGGGCCACGAGCGAGGGTACGAGG AGGGGACGAGGGTCGGGGCCGCGGGAAAG____CGAAGGGCGGGGCCACGAGCGAGGGTACGAGG GCGGA G MYO15B Ensembl:ENSG00000266714 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75589360..75589557 26863196 MeRIP-seq:(Medium) rs1236209522 Functional Loss DEL dbSNP153 30..33 33 - - - 100372 RMVar_ID_100372 Human_SNP_ID_632893493 m1A Human chr17 + 75589493 75589467 75589494 GCGGGGTCACGAGAGAGGTGACGAGGGCCGGGACCACCAGAGAGGGTACGAGGGGTGGGGCCGTG GCGGGGT___________________________CACCAGAGAGGGTACGAGGGGTGGGGCCGTG TCACGAGAGAGGTGACGAGGGCCGGGAC T MYO15B Ensembl:ENSG00000266714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75589402..75589506 26863196 MeRIP-seq:(Medium) rs1455053198 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_3541868,Human_RBP_ID_5144387 100373 RMVar_ID_100373 Human_SNP_ID_632908120 m1A Human chr17 - 75631459 75631459 75631459 GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGACTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGTCTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC T A RECQL5 Ensembl:ENSG00000108469 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs820196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_900739,Human_RBP_ID_18708661,Human_RBP_ID_27814280 Human_Splice_Rec_1867855,Human_Splice_Rec_1867891,Human_Splice_Rec_1867927,Human_Splice_Rec_1867961 GWAS_ID_13185,GWAS_ID_13186,GWAS_ID_13187,GWAS_ID_13188,GWAS_ID_13189,GWAS_ID_13190,GWAS_ID_13191,GWAS_ID_13192 RMVar_hsa_circ_117920,RMVar_hsa_circ_62148,RMVar_hsa_circ_187057,RMVar_hsa_circ_82823,RMVar_hsa_circ_187056 100374 RMVar_ID_100374 Human_SNP_ID_632908121 m1A Human chr17 - 75631459 75631459 75631459 GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGACTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGGCTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC T C RECQL5 Ensembl:ENSG00000108469 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs820196 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_900739,Human_RBP_ID_18708661,Human_RBP_ID_27814280 Human_Splice_Rec_1867855,Human_Splice_Rec_1867891,Human_Splice_Rec_1867927,Human_Splice_Rec_1867961 GWAS_ID_13185,GWAS_ID_13186,GWAS_ID_13187,GWAS_ID_13188,GWAS_ID_13189,GWAS_ID_13190,GWAS_ID_13191,GWAS_ID_13192 RMVar_hsa_circ_117920,RMVar_hsa_circ_62148,RMVar_hsa_circ_187057,RMVar_hsa_circ_82823,RMVar_hsa_circ_187056 100375 RMVar_ID_100375 Human_SNP_ID_632916917 m1A Human chr17 - 75665143 75665143 75665143 CAGGTAACAAGGACGTCTTTGTGTGCATGCCCACAGGGGCAGGAAAATCCCTATGCTATCAGCTC CAGGTAACAAGGACGTCTTTGTGTGCATGCCCTCAGGGGCAGGAAAATCCCTATGCTATCAGCTC T A RECQL5 Ensembl:ENSG00000108469 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75665136..75666591 32194978 MeRIP-seq:(Medium) rs753625950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904030,Human_RBP_ID_9378956,Human_RBP_ID_18989200 Human_Splice_Rec_1867879,Human_Splice_Rec_1867914,Human_Splice_Rec_1867915,Human_Splice_Rec_1867980,Human_Splice_Rec_1867981,Human_Splice_Rec_1868012,Human_Splice_Rec_1868013,Human_Splice_Rec_1868024,Human_Splice_Rec_1868025,Human_Splice_Rec_1868040,Human_Splice_Rec_1868041 RMVar_hsa_circ_7269,RMVar_hsa_circ_117920,RMVar_hsa_circ_187057,RMVar_hsa_circ_30440,RMVar_hsa_circ_292896,RMVar_hsa_circ_187058,RMVar_hsa_circ_352216 100376 RMVar_ID_100376 Human_SNP_ID_632916918 m1A Human chr17 - 75665143 75665143 75665143 CAGGTAACAAGGACGTCTTTGTGTGCATGCCCACAGGGGCAGGAAAATCCCTATGCTATCAGCTC CAGGTAACAAGGACGTCTTTGTGTGCATGCCCGCAGGGGCAGGAAAATCCCTATGCTATCAGCTC T C RECQL5 Ensembl:ENSG00000108469 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75665136..75666591 32194978 MeRIP-seq:(Medium) rs753625950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904030,Human_RBP_ID_9378956,Human_RBP_ID_18989200 Human_Splice_Rec_1867879,Human_Splice_Rec_1867914,Human_Splice_Rec_1867915,Human_Splice_Rec_1867980,Human_Splice_Rec_1867981,Human_Splice_Rec_1868012,Human_Splice_Rec_1868013,Human_Splice_Rec_1868024,Human_Splice_Rec_1868025,Human_Splice_Rec_1868040,Human_Splice_Rec_1868041 RMVar_hsa_circ_7269,RMVar_hsa_circ_117920,RMVar_hsa_circ_187057,RMVar_hsa_circ_30440,RMVar_hsa_circ_292896,RMVar_hsa_circ_187058,RMVar_hsa_circ_352216 100377 RMVar_ID_100377 Human_SNP_ID_632917649 m1A Human chr17 - 75667402 75667402 75667402 TCGGGCTCTGAATCTTCCGCGTAAACTGCGAGAGACGACAGAACATTCTTCTTCCCCGCCATCTT TCGGGCTCTGAATCTTCCGCGTAAACTGCGAGGGACGACAGAACATTCTTCTTCCCCGCCATCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:75667351..75667519;chr17:75667351..75668084;chr17:75667351..75667534 26863196 MeRIP-seq:(Medium) rs528872253 Functional Loss SNV dbSNP153 33..33 33 - - - 100378 RMVar_ID_100378 Human_SNP_ID_632917674 m1A Human chr17 + 75667469 75667469 75667469 CTGATGGCGAGGCTGGAATCGAGGCGGTGGGCAGCGCGGCTGGTAAGGCCCAAGTGCGAAGCTGG CTGATGGCGAGGCTGGAATCGAGGCGGTGGGCCGCGCGGCTGGTAAGGCCCAAGTGCGAAGCTGG A C SAP30BP Ensembl:ENSG00000161526 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:75667351..75667551 26863196 MeRIP-seq:(Medium) rs1488982867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237967,Human_RBP_ID_9376832,Human_RBP_ID_18419730,Human_RBP_ID_18992274,Human_RBP_ID_22061640,Human_RBP_ID_22959657,Human_RBP_ID_26330874 Human_Splice_Rec_1868073,Human_Splice_Rec_1868081,Human_Splice_Rec_1868101,Human_Splice_Rec_1868109,Human_Splice_Rec_1868127,Human_Splice_Rec_1868131,Human_Splice_Rec_1868141,Human_Splice_Rec_1868157,Human_Splice_Rec_1868171,Human_Splice_Rec_1868179,Human_Splice_Rec_1868189,Human_Splice_Rec_1868201,Human_Splice_Rec_1868221,Human_Splice_Rec_1868235,Human_Splice_Rec_1868253,Human_Splice_Rec_1868273 100379 RMVar_ID_100379 Human_SNP_ID_632917675 m1A Human chr17 - 75667477 75667477 75667477 TCCCCCTTCCAGCTTCGCACTTGGGCCTTACCAGCCGCGCTGCCCACCGCCTCGATTCCAGCCTC TCCCCCTTCCAGCTTCGCACTTGGGCCTTACCGGCCGCGCTGCCCACCGCCTCGATTCCAGCCTC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:75667376..75667500 26863410 MeRIP-seq:(Medium) rs1216939334 Functional Loss SNV dbSNP153 33..33 33 - - - 100380 RMVar_ID_100380 Human_SNP_ID_632917963 m1A Human chr17 + 75668454 75668454 75668454 GGCCACTCAAATCTCTGGACATTTTTTCTTACATTGTAACTCTTGTTTTTTTTTTCTTGCTTTTT GGCCACTCAAATCTCTGGACATTTTTTCTTACGTTGTAACTCTTGTTTTTTTTTTCTTGCTTTTT A G SAP30BP Ensembl:ENSG00000161526 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75668452..75671919 26863196 MeRIP-seq:(Medium) rs1007624210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6643837 100381 RMVar_ID_100381 Human_SNP_ID_632918321 m1A Human chr17 + 75669552 75669552 75669552 GGCGTGAGCCACTGCTCCTGGCCGATTTTTAAAATTTAAAAAAAAATTTTTTGTAGAGACGTTGT GGCGTGAGCCACTGCTCCTGGCCGATTTTTAATATTTAAAAAAAAATTTTTTGTAGAGACGTTGT A T SAP30BP Ensembl:ENSG00000161526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75668465..75671875 26863196 MeRIP-seq:(Medium) rs1011684921 Functional Loss SNV dbSNP153 33..33 33 - - - 100382 RMVar_ID_100382 Human_SNP_ID_632928255 m1A Human chr17 + 75706551 75706551 75706551 TGACCTGAGGGGCCACCCTAGGACTTGAAAGGACCGTGCAGCCCAGTGACCACTGCCCAGTGGGA TGACCTGAGGGGCCACCCTAGGACTTGAAAGGTCCGTGCAGCCCAGTGACCACTGCCCAGTGGGA A T SAP30BP Ensembl:ENSG00000161526 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75706501..75706575 32194978 MeRIP-seq:(Medium) rs775699912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_900755,Human_RBP_ID_1542165,Human_RBP_ID_8232468,Human_RBP_ID_9376840,Human_RBP_ID_13164045,Human_RBP_ID_18708742,Human_RBP_ID_18989204,Human_RBP_ID_21890303,Human_RBP_ID_26332373,Human_RBP_ID_26460945,Human_RBP_ID_26971135,Human_RBP_ID_27259727,Human_RBP_ID_27814284 100383 RMVar_ID_100383 Human_SNP_ID_632945233 m1A Human chr17 + 75762760 75762760 75762760 CCCGGAGGCTTTCCTTGCCCAGCGCCCGGGCCACTTCTTCACATTGGCGCCGCCGCACAGGGTAC CCCGGAGGCTTTCCTTGCCCAGCGCCCGGGCCCCTTCTTCACATTGGCGCCGCCGCACAGGGTAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75762661..75762795 26863196 MeRIP-seq:(Medium) rs748015014 Functional Loss SNV dbSNP153 33..33 33 - - - 100384 RMVar_ID_100384 Human_SNP_ID_632945489 m1A Human chr17 - 75763399 75763399 75763399 CTCCCTGGCTTCAGTGCAGTGGTGGTCAGCTCAGTGCCCCTGGGGGGTGGCCTGTCCAGCTCAGC CTCCCTGGCTTCAGTGCAGTGGTGGTCAGCTCGGTGCCCCTGGGGGGTGGCCTGTCCAGCTCAGC T C GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75763301..75763450 32194978 MeRIP-seq:(Medium) rs766401384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499942,Human_RBP_ID_5467003,Human_RBP_ID_18190945,Human_RBP_ID_22443900 Human_Splice_Rec_1868814,Human_Splice_Rec_1868815,Human_Splice_Rec_1868842,Human_Splice_Rec_1868843,Human_Splice_Rec_1868856,Human_Splice_Rec_1868857,Human_Splice_Rec_1868866,Human_Splice_Rec_1868874 Human_miRNA_ID_172375,Human_miRNA_ID_2469806 RMVar_hsa_circ_126195,RMVar_hsa_circ_187089,RMVar_hsa_circ_83145,RMVar_hsa_circ_187090 100385 RMVar_ID_100385 Human_SNP_ID_632946094 m1A Human chr17 - 75765021 75765021 75765021 CGAGCTGGCCGTGTCAGCGCCGGGCCGCGTCAACCTCATCGGGGAACACACGGACTACAACCAGG CGAGCTGGCCGTGTCAGCGCCGGGCCGCGTCAGCCTCATCGGGGAACACACGGACTACAACCAGG T C GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75764001..75765200 26863196 MeRIP-seq:(Medium) rs536209426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464787 Human_Splice_Rec_1868811,Human_Splice_Rec_1868839,Human_Splice_Rec_1868863,Human_Splice_Rec_1868869,Human_Splice_Rec_1868875 Clinvar_Rec_616 RMVar_hsa_circ_75205 100386 RMVar_ID_100386 Human_SNP_ID_632946095 m1A Human chr17 - 75765021 75765021 75765021 CGAGCTGGCCGTGTCAGCGCCGGGCCGCGTCAACCTCATCGGGGAACACACGGACTACAACCAGG CGAGCTGGCCGTGTCAGCGCCGGGCCGCGTCACCCTCATCGGGGAACACACGGACTACAACCAGG T G GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75764001..75765200 26863196 MeRIP-seq:(Medium) rs536209426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464787 Human_Splice_Rec_1868811,Human_Splice_Rec_1868839,Human_Splice_Rec_1868863,Human_Splice_Rec_1868869,Human_Splice_Rec_1868875 Clinvar_Rec_616 RMVar_hsa_circ_75205 100387 RMVar_ID_100387 Human_SNP_ID_632946114 m1A Human chr17 - 75765051 75765051 75765051 AGCCTTCCGGGAGGAGTTCGGGGCCGAGCCCGAGCTGGCCGTGTCAGCGCCGGGCCGCGTCAACC AGCCTTCCGGGAGGAGTTCGGGGCCGAGCCCGGGCTGGCCGTGTCAGCGCCGGGCCGCGTCAACC T C GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75765013..75765142 26863196 MeRIP-seq:(Medium) rs1333158089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768198,Human_RBP_ID_4464787,Human_RBP_ID_22444953 Human_Splice_Rec_1868811,Human_Splice_Rec_1868839,Human_Splice_Rec_1868863,Human_Splice_Rec_1868869,Human_Splice_Rec_1868875 RMVar_hsa_circ_75205 100388 RMVar_ID_100388 Human_SNP_ID_632949740 m1A Human chr17 - 75777669 75777669 75777669 AGTACCGAAGTTCTTTTTCTTGTGGCATTTGTATTATAAAAACTTGGTGTGGGGGAGGAGCACAA AGTACCGAAGTTCTTTTTCTTGTGGCATTTGTGTTATAAAAACTTGGTGTGGGGGAGGAGCACAA T C H3-3B Ensembl:ENSG00000132475 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75777618..75777767 32194978 MeRIP-seq:(Medium) rs900103151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499981,Human_RBP_ID_1184264,Human_RBP_ID_1869099,Human_RBP_ID_2522784,Human_RBP_ID_6644056,Human_RBP_ID_9076279,Human_RBP_ID_13164329,Human_RBP_ID_17900897,Human_RBP_ID_23749333,Human_RBP_ID_27669507 Human_miRNA_ID_753325,Human_miRNA_ID_1086289,Human_miRNA_ID_1117589,Human_miRNA_ID_1124759,Human_miRNA_ID_1175845,Human_miRNA_ID_1628507,Human_miRNA_ID_1669005 RMVar_hsa_circ_266271 100389 RMVar_ID_100389 Human_SNP_ID_632950050 m1A Human chr17 + 75778326 75778325 75778327 TATCAACTCTAGTACCTTAATAGCTACCCAACAAGTCATTAACATACAGAAACATGCATCATGAG TATCAACTCTAGTACCTTAATAGCTACCCAAC__GTCATTAACATACAGAAACATGCATCATGAG CAA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75778275..75778421 26863196 MeRIP-seq:(Medium) rs142703331 Functional Loss DEL dbSNP153 33..34 33 - - - 100390 RMVar_ID_100390 Human_SNP_ID_632950241 m1A Human chr17 - 75778717 75778717 75778717 AATAGTGCGGCTCTCGTCCTCAACAGGAGGCTAGCGAAGCGTACCTGGTGGGTCTGTTCGAAGAT AATAGTGCGGCTCTCGTCCTCAACAGGAGGCTGGCGAAGCGTACCTGGTGGGTCTGTTCGAAGAT T C H3-3B Ensembl:ENSG00000132475 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:75778426..75778725;chr17:75778626..75778725 32194978 MeRIP-seq:(Medium) rs776430564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237823,Human_RBP_ID_500016,Human_RBP_ID_768509,Human_RBP_ID_4466805,Human_RBP_ID_5143652,Human_RBP_ID_5363120,Human_RBP_ID_6644105,Human_RBP_ID_19079976,Human_RBP_ID_22443161,Human_RBP_ID_22760950,Human_RBP_ID_26782585 Human_Splice_Rec_1868882,Human_Splice_Rec_1868886,Human_Splice_Rec_1868892,Human_Splice_Rec_1868898,Human_Splice_Rec_1868904,Human_Splice_Rec_1868910,Human_Splice_Rec_1868916,Human_Splice_Rec_1868922,Human_Splice_Rec_1868930 RMVar_hsa_circ_266271 100391 RMVar_ID_100391 Human_SNP_ID_632950494 m1A Human chr17 + 75779148 75779148 75779148 TGTTTGCGGGGGGCTTTCCCACCGGTGGACTTACGAGCAGTCTGCTTGGTTCGGGCCATTTTCTT TGTTTGCGGGGGGCTTTCCCACCGGTGGACTTCCGAGCAGTCTGCTTGGTTCGGGCCATTTTCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75779100..75779298 26863196 MeRIP-seq:(Medium) rs1311907108 Functional Loss SNV dbSNP153 33..33 33 - - - 100392 RMVar_ID_100392 Human_SNP_ID_632950495 m1A Human chr17 + 75779151 75779151 75779151 TTGCGGGGGGCTTTCCCACCGGTGGACTTACGAGCAGTCTGCTTGGTTCGGGCCATTTTCTTTCA TTGCGGGGGGCTTTCCCACCGGTGGACTTACGTGCAGTCTGCTTGGTTCGGGCCATTTTCTTTCA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75779101..75779200 26863196 MeRIP-seq:(Medium) rs746366357 Functional Loss SNV dbSNP153 33..33 33 - - - 100393 RMVar_ID_100393 Human_SNP_ID_632950505 m1A Human chr17 - 75779181 75779180 75779182 CGGCCTTATCTTCGGGGCGTCTTTCTTAGGTGAAAGAAAATGGCCCGAACCAAGCAGACTGCTCG CGGCCTTATCTTCGGGGCGTCTTTCTTAGGT__AAGAAAATGGCCCGAACCAAGCAGACTGCTCG TTC T H3-3B Ensembl:ENSG00000132475 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:75779176..75779200 26863196 MeRIP-seq:(Medium) rs1265757630 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_898735,Human_RBP_ID_1542224,Human_RBP_ID_4465684,Human_RBP_ID_9326824,Human_RBP_ID_19083910,Human_RBP_ID_22475175 Human_Splice_Rec_1868878,Human_Splice_Rec_1868888,Human_Splice_Rec_1868894,Human_Splice_Rec_1868900,Human_Splice_Rec_1868906,Human_Splice_Rec_1868912,Human_Splice_Rec_1868918,Human_Splice_Rec_1868924,Human_Splice_Rec_1868928 RMVar_hsa_circ_187091,RMVar_hsa_circ_338647,RMVar_hsa_circ_378374 100394 RMVar_ID_100394 Human_SNP_ID_632950508 m1A Human chr17 - 75779181 75779181 75779181 CGGCCTTATCTTCGGGGCGTCTTTCTTAGGTGAAAGAAAATGGCCCGAACCAAGCAGACTGCTCG CGGCCTTATCTTCGGGGCGTCTTTCTTAGGTGGAAGAAAATGGCCCGAACCAAGCAGACTGCTCG T C H3-3B Ensembl:ENSG00000132475 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:75779176..75779200 26863196 MeRIP-seq:(Medium) rs1372470728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898735,Human_RBP_ID_1542224,Human_RBP_ID_4465684,Human_RBP_ID_9326824,Human_RBP_ID_19083910,Human_RBP_ID_22475175 Human_Splice_Rec_1868878,Human_Splice_Rec_1868888,Human_Splice_Rec_1868894,Human_Splice_Rec_1868900,Human_Splice_Rec_1868906,Human_Splice_Rec_1868912,Human_Splice_Rec_1868918,Human_Splice_Rec_1868924,Human_Splice_Rec_1868928 RMVar_hsa_circ_187091,RMVar_hsa_circ_338647,RMVar_hsa_circ_378374 100395 RMVar_ID_100395 Human_SNP_ID_632950509 m1A Human chr17 + 75779183 75779183 75779183 AGCAGTCTGCTTGGTTCGGGCCATTTTCTTTCACCTAAGAAAGACGCCCCGAAGATAAGGCCGCC AGCAGTCTGCTTGGTTCGGGCCATTTTCTTTCGCCTAAGAAAGACGCCCCGAAGATAAGGCCGCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:75778853..75779249 26863410 MeRIP-seq:(Medium) rs797020985 Functional Loss SNV dbSNP153 33..33 33 - - - 100396 RMVar_ID_100396 Human_SNP_ID_632950857 m1A Human chr17 - 75779706 75779706 75779706 TTTCGCTCGTCGACTGCGGCTCTTCCTCGGGCAGCGGAAGCGGCGCGGCGGTCGGAGAAGTGGCC TTTCGCTCGTCGACTGCGGCTCTTCCTCGGGCGGCGGAAGCGGCGCGGCGGTCGGAGAAGTGGCC T C H3-3B Ensembl:ENSG00000132475 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75779651..75779775 32194978 MeRIP-seq:(Medium) rs1411692099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50615,Human_RBP_ID_237828,Human_RBP_ID_500023,Human_RBP_ID_768517,Human_RBP_ID_1542227,Human_RBP_ID_4464790,Human_RBP_ID_5319239,Human_RBP_ID_5420496,Human_RBP_ID_5497792,Human_RBP_ID_6644112,Human_RBP_ID_8463196,Human_RBP_ID_8822172,Human_RBP_ID_9076300,Human_RBP_ID_9326829,Human_RBP_ID_13164369,Human_RBP_ID_22061642,Human_RBP_ID_22221172,Human_RBP_ID_22444959,Human_RBP_ID_22806721,Human_RBP_ID_23114392,Human_RBP_ID_23129709,Human_RBP_ID_26646112,Human_RBP_ID_27259767,Human_RBP_ID_27561414,Human_RBP_ID_27838531 Human_Splice_Rec_1868877,Human_Splice_Rec_1868883,Human_Splice_Rec_1868887,Human_Splice_Rec_1868893,Human_Splice_Rec_1868899,Human_Splice_Rec_1868905,Human_Splice_Rec_1868923,Human_Splice_Rec_1868927 100397 RMVar_ID_100397 Human_SNP_ID_632950866 m1A Human chr17 + 75779724 75779724 75779724 CGCGCCGCTTCCGCTGCCCGAGGAAGAGCCGCAGTCGACGAGCGAAAAACCAGCACCGCCCAACG CGCGCCGCTTCCGCTGCCCGAGGAAGAGCCGCTGTCGACGAGCGAAAAACCAGCACCGCCCAACG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:75779544..75779775;chr17:75779585..75779775;chr17:75779612..75779775;chr17:75779629..75779775 26863196 MeRIP-seq:(Medium) rs1567786059 Functional Loss SNV dbSNP153 33..33 33 - - - 100398 RMVar_ID_100398 Human_SNP_ID_632950870 m1A Human chr17 - 75779726 75779726 75779726 TTCGTTGGGCGGTGCTGGTTTTTCGCTCGTCGACTGCGGCTCTTCCTCGGGCAGCGGAAGCGGCG TTCGTTGGGCGGTGCTGGTTTTTCGCTCGTCGGCTGCGGCTCTTCCTCGGGCAGCGGAAGCGGCG T C H3-3B Ensembl:ENSG00000132475 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr17:75779607..75779775;chr17:75779603..75779775;chr17:75779676..75779775 26863196 MeRIP-seq:(Medium) rs1038248658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237828,Human_RBP_ID_278610,Human_RBP_ID_500023,Human_RBP_ID_768517,Human_RBP_ID_1010502,Human_RBP_ID_1184271,Human_RBP_ID_1542227,Human_RBP_ID_1869121,Human_RBP_ID_4464790,Human_RBP_ID_5319239,Human_RBP_ID_5420754,Human_RBP_ID_5441912,Human_RBP_ID_5467004,Human_RBP_ID_5497793,Human_RBP_ID_6644112,Human_RBP_ID_8463196,Human_RBP_ID_8822173,Human_RBP_ID_9076300,Human_RBP_ID_9288197,Human_RBP_ID_9326829,Human_RBP_ID_13164372,Human_RBP_ID_18439662,Human_RBP_ID_18708794,Human_RBP_ID_22061643,Human_RBP_ID_22221172,Human_RBP_ID_22444959,Human_RBP_ID_23114392,Human_RBP_ID_23129710,Human_RBP_ID_23749365,Human_RBP_ID_26971177,Human_RBP_ID_27561414,Human_RBP_ID_27669526,Human_RBP_ID_27838531 Human_Splice_Rec_1868877,Human_Splice_Rec_1868883,Human_Splice_Rec_1868887,Human_Splice_Rec_1868893,Human_Splice_Rec_1868899,Human_Splice_Rec_1868905,Human_Splice_Rec_1868923,Human_Splice_Rec_1868927 100399 RMVar_ID_100399 Human_SNP_ID_632952554 m1A Human chr17 + 75784887 75784887 75784887 CGGCGAAGAGGCAGGAAGACAAGACCATGTCGAAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCC CGGCGAAGAGGCAGGAAGACAAGACCATGTCGGAGGGCCCCGGGCCCGGCGGCTCCGCAGCTTCC A G UNK Ensembl:ENSG00000132478 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75784851..75784950;chr17:75784851..75785081 26863196 MeRIP-seq:(Medium) rs769276178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465689,Human_RBP_ID_17378523,Human_RBP_ID_18419731,Human_RBP_ID_22959658 Human_Splice_Rec_1868931,Human_Splice_Rec_1868961,Human_Splice_Rec_1868963,Human_Splice_Rec_1868967,Human_Splice_Rec_1868973 100400 RMVar_ID_100400 Human_SNP_ID_632954103 m1A Human chr17 + 75790541 75790541 75790541 GTGGTCCTGGATACTCAGGAGGCCGAGGTGGGAGGATCCCTGAGCCCAGGAGATAGAGGCTACAG GTGGTCCTGGATACTCAGGAGGCCGAGGTGGGGGGATCCCTGAGCCCAGGAGATAGAGGCTACAG A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75790538..75790699 26863196 MeRIP-seq:(Medium) rs1262172486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13164578 100401 RMVar_ID_100401 Human_SNP_ID_632954401 m1A Human chr17 + 75791856 75791856 75791856 TATCATCCTACAAAGACTGTGACTTATTGGTGAGGGCAGCTGGACAACTCTGAGAGCAACTTAGA TATCATCCTACAAAGACTGTGACTTATTGGTGGGGGCAGCTGGACAACTCTGAGAGCAACTTAGA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75791854..75791937 26863196 MeRIP-seq:(Medium) rs1389833828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500031,Human_RBP_ID_1542255,Human_RBP_ID_1869143,Human_RBP_ID_3537362,Human_RBP_ID_6644159,Human_RBP_ID_8463228,Human_RBP_ID_13164629,Human_RBP_ID_18708803,Human_RBP_ID_23749400 Human_Splice_Rec_1868962,Human_Splice_Rec_1868968 RMVar_hsa_circ_347610,RMVar_hsa_circ_359730,RMVar_hsa_circ_187092 100402 RMVar_ID_100402 Human_SNP_ID_632959917 m1A Human chr17 + 75813855 75813855 75813855 ACGGAGACGCCTGCCAGTACTGCCACACCCGCACCGAGCAGCAGTTCCACCCCGAGGTGGGCCCC ACGGAGACGCCTGCCAGTACTGCCACACCCGCCCCGAGCAGCAGTTCCACCCCGAGGTGGGCCCC A C UNK Ensembl:ENSG00000132478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75813805..75813912 26863196 MeRIP-seq:(Medium) rs111230833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1868940,Human_Splice_Rec_1868941,Human_Splice_Rec_1868986,Human_Splice_Rec_1868987 RMVar_hsa_circ_51779,RMVar_hsa_circ_187097,RMVar_hsa_circ_285228,RMVar_hsa_circ_342599,RMVar_hsa_circ_187095,RMVar_hsa_circ_114230,RMVar_hsa_circ_336751,RMVar_hsa_circ_374925,RMVar_hsa_circ_187098 100403 RMVar_ID_100403 Human_SNP_ID_632963053 m1A Human chr17 - 75825475 75825475 75825475 CACACACACACGCACACAGGCGTCCGCCCAGAACAGGGCGGGACACCAGCTGCACTCAGAGAGCA CACACACACACGCACACAGGCGTCCGCCCAGAGCAGGGCGGGACACCAGCTGCACTCAGAGAGCA T C lnc-SRP68-1 RNACentral:URS00008BF89B lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75825382..75825486 32194978 MeRIP-seq:(Medium) rs1295015742 Functional Loss SNV dbSNP153 33..33 33 - - - 100404 RMVar_ID_100404 Human_SNP_ID_632966059 m1A Human chr17 - 75834463 75834463 75834463 CTGGTGATCGGCAAGTTGCCCGCCCAGCTGGCATGGGAGGCCCTGGAGCAGCGGGTAGGGGCCGT CTGGTGATCGGCAAGTTGCCCGCCCAGCTGGCTTGGGAGGCCCTGGAGCAGCGGGTAGGGGCCGT T A UNC13D Ensembl:ENSG00000092929 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75834369..75834486 26863196 MeRIP-seq:(Medium) rs951593554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8824957,Human_RBP_ID_9290306,Human_RBP_ID_18989222,Human_RBP_ID_22443169 Human_Splice_Rec_1869048,Human_Splice_Rec_1869110,Human_Splice_Rec_1869180,Human_Splice_Rec_1869188 RMVar_hsa_circ_27770,RMVar_hsa_circ_110462,RMVar_hsa_circ_123496,RMVar_hsa_circ_187102,RMVar_hsa_circ_187103 100405 RMVar_ID_100405 Human_SNP_ID_632967943 m1A Human chr17 + 75839888 75839888 75839888 GTCGGATAGGTCCTTCTGTGTGGCGTGCAGAAAGAGGACGGTGGCAGCCTGGGGACTCAGCGACC GTCGGATAGGTCCTTCTGTGTGGCGTGCAGAAGGAGGACGGTGGCAGCCTGGGGACTCAGCGACC A G lnc-UNK-1 RNACentral:URS00008B837D lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75839809..75839926 26863196 MeRIP-seq:(Medium) rs369536831 Functional Loss SNV dbSNP153 33..33 33 - - - 100406 RMVar_ID_100406 Human_SNP_ID_632969614 m1A Human chr17 - 75844274 75844273 75844274 GCCCTCCCTTCTTGCGCCAGGCCATCAAGATAAGGCGCCGCAGAGTCAGAGATCTACAGGATCCC GCCCTCCCTTCTTGCGCCAGGCCATCAAGATA_GGCGCCGCAGAGTCAGAGATCTACAGGATCCC CT C UNC13D Ensembl:ENSG00000092929 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75844189..75844358 26863196 MeRIP-seq:(Medium) rs1384017743 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18470111 Human_Splice_Rec_1869005,Human_Splice_Rec_1869067,Human_Splice_Rec_1869141,Human_Splice_Rec_1869189,Human_Splice_Rec_1869239,Human_Splice_Rec_1869294,Human_Splice_Rec_1869295 RMVar_hsa_circ_95033,RMVar_hsa_circ_187108,RMVar_hsa_circ_104703,RMVar_hsa_circ_187109 100407 RMVar_ID_100407 Human_SNP_ID_632969636 m1A Human chr17 + 75844324 75844324 75844324 GCAAGAAGGGAGGGCGCTGCTGCGGATGGGAGAGGAGTGTCGCCATGGTGGCCTTCTCTGCCCTT GCAAGAAGGGAGGGCGCTGCTGCGGATGGGAGGGGAGTGTCGCCATGGTGGCCTTCTCTGCCCTT A G lnc-UNK-1 RNACentral:URS00008B837D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75844275..75844403 26863196 MeRIP-seq:(Medium) rs1322153234 Functional Loss SNV dbSNP153 33..33 33 - - - 100408 RMVar_ID_100408 Human_SNP_ID_632970239 m1A Human chr17 + 75846390 75846388 75846390 TGAGGCTGAGTGTAGCAGTGGGTGCCAGACTGAGGGAGCTGGACTGCGGTGGAGGAGGTGGCCAG TGAGGCTGAGTGTAGCAGTGGGTGCCAGACT__GGGAGCTGGACTGCGGTGGAGGAGGTGGCCAG TGA T lnc-UNK-1 RNACentral:URS00008B837D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75846339..75846574 26863196 MeRIP-seq:(Medium) rs1291157992 Functional Loss DEL dbSNP153 32..33 33 - - - 100409 RMVar_ID_100409 Human_SNP_ID_632970448 m1A Human chr17 - 75846910 75846910 75846910 ACCCAGGCAATCCTCACAACGTCTACATGCCCACGGTGAGAGGGCTTGGCAGTGCCGGTGCAGCC ACCCAGGCAATCCTCACAACGTCTACATGCCCCCGGTGAGAGGGCTTGGCAGTGCCGGTGCAGCC T G WBP2 Ensembl:ENSG00000132471 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:75846901..75846950 26863196 MeRIP-seq:(Medium) rs1359353040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17900963 Human_Splice_Rec_1869318,Human_Splice_Rec_1869319,Human_Splice_Rec_1869344,Human_Splice_Rec_1869345,Human_Splice_Rec_1869360,Human_Splice_Rec_1869361,Human_Splice_Rec_1869367,Human_Splice_Rec_1869394,Human_Splice_Rec_1869395,Human_Splice_Rec_1869402,Human_Splice_Rec_1869403,Human_Splice_Rec_1869420,Human_Splice_Rec_1869421,Human_Splice_Rec_1869432,Human_Splice_Rec_1869433,Human_Splice_Rec_1869438,Human_Splice_Rec_1869439 100410 RMVar_ID_100410 Human_SNP_ID_632970453 m1A Human chr17 + 75846915 75846915 75846915 CACCGGCACTGCCAAGCCCTCTCACCGTGGGCATGTAGACGTTGTGAGGATTGCCTGGGTTGTAA CACCGGCACTGCCAAGCCCTCTCACCGTGGGCGTGTAGACGTTGTGAGGATTGCCTGGGTTGTAA A G lnc-UNK-1 RNACentral:URS00008B837D lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75846263..75847019 26863196 MeRIP-seq:(Medium) rs200534175 Functional Loss SNV dbSNP153 33..33 33 - - - 100411 RMVar_ID_100411 Human_SNP_ID_632970687 m1A Human chr17 + 75847539 75847539 75847539 TCGGGGCCGCTGACCGGAGGTTCCATGGGCCCAGGGTAGGGCGGTGGTGGGGGCTGCACGTATCC TCGGGGCCGCTGACCGGAGGTTCCATGGGCCCCGGGTAGGGCGGTGGTGGGGGCTGCACGTATCC A C lnc-UNK-1 RNACentral:URS00008B837D lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:75847417..75847668;chr17:75847476..75847625;chr17:75847460..75847668;chr17:75847448..75847580;chr17:75847451..75847625 26863196 MeRIP-seq:(Medium) rs1377950178 Functional Loss SNV dbSNP153 33..33 33 - - - 100412 RMVar_ID_100412 Human_SNP_ID_632971964 m1A Human chr17 - 75851650 75851650 75851650 TCACAGCATCCTAATGTCCTATGATCACGTGGAACTCACATTCAATGACATGAAGAACGTGCCAG TCACAGCATCCTAATGTCCTATGATCACGTGGTACTCACATTCAATGACATGAAGAACGTGCCAG T A WBP2 Ensembl:ENSG00000132471 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75851601..75851718 26863196 MeRIP-seq:(Medium) rs1216816120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1542327,Human_RBP_ID_1869227,Human_RBP_ID_17900968,Human_RBP_ID_18708868 Human_Splice_Rec_1869308,Human_Splice_Rec_1869309,Human_Splice_Rec_1869322,Human_Splice_Rec_1869323,Human_Splice_Rec_1869334,Human_Splice_Rec_1869335,Human_Splice_Rec_1869350,Human_Splice_Rec_1869351,Human_Splice_Rec_1869363,Human_Splice_Rec_1869370,Human_Splice_Rec_1869371,Human_Splice_Rec_1869384,Human_Splice_Rec_1869385,Human_Splice_Rec_1869410,Human_Splice_Rec_1869411,Human_Splice_Rec_1869424,Human_Splice_Rec_1869425,Human_Splice_Rec_1869442,Human_Splice_Rec_1869443,Human_Splice_Rec_1869466,Human_Splice_Rec_1869467,Human_Splice_Rec_1869476,Human_Splice_Rec_1869477,Human_Splice_Rec_1869482,Human_Splice_Rec_1869483,Human_Splice_Rec_1869488,Human_Splice_Rec_1869489,Human_Splice_Rec_1869492 100413 RMVar_ID_100413 Human_SNP_ID_632978469 m1A Human chr17 + 75874749 75874749 75874749 GAAGGCCAAGGCACGGTCAGCGTATTCCAGGCAGACCCCAACCGTGGGCGAGAAGGGGTGGGGCA GAAGGCCAAGGCACGGTCAGCGTATTCCAGGCCGACCCCAACCGTGGGCGAGAAGGGGTGGGGCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75874310..75875009 32194978 MeRIP-seq:(Medium) rs947012028 Functional Loss SNV dbSNP153 33..33 33 - - - 100414 RMVar_ID_100414 Human_SNP_ID_632978731 m1A Human chr17 + 75875473 75875473 75875473 TTCGTACTCTCGAGGTCTTGGGGCTCAGCATCAGCTGTAGAAGAGGAGACAGTGGTGAGAACGCC TTCGTACTCTCGAGGTCTTGGGGCTCAGCATCCGCTGTAGAAGAGGAGACAGTGGTGAGAACGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75875451..75875475 26863196 MeRIP-seq:(Medium) rs182494507 Functional Loss SNV dbSNP153 33..33 33 - - - 100415 RMVar_ID_100415 Human_SNP_ID_632979706 m1A Human chr17 + 75878215 75878215 75878215 CGCGGGCCACGGCTCGGGAGCGCAGGGGGCCGACGGCTCCGGGACACTGGGCAGCGCGCTGGGTG CGCGGGCCACGGCTCGGGAGCGCAGGGGGCCGCCGGCTCCGGGACACTGGGCAGCGCGCTGGGTG A C AC087289.5 Ensembl:ENSG00000267801 lincRNA exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr17:75878130..75878270;chr17:75878008..75878455 26863196,26863410 MeRIP-seq:(Medium) rs537756893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8193976 100416 RMVar_ID_100416 Human_SNP_ID_632982871 m1A Human chr17 - 75889552 75889552 75889552 TGGGTGTGGGACTTTGGGGCAGCCGTGTGTGCAGGTGTCGGCACAGGCTAGCTCCTCCTGGTTTG TGGGTGTGGGACTTTGGGGCAGCCGTGTGTGCGGGTGTCGGCACAGGCTAGCTCCTCCTGGTTTG T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75889501..75889575 32194978 MeRIP-seq:(Medium) rs1480609529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4451627,Human_RBP_ID_6644395,Human_RBP_ID_13165699 100417 RMVar_ID_100417 Human_SNP_ID_632983143 m1A Human chr17 + 75890675 75890675 75890675 TCCCCCAACCTCCCATCTCTTTCTGAGTTAACAGAGAGGCCAACAGCTGGTCCTCCAGTCCCCAA TCCCCCAACCTCCCATCTCTTTCTGAGTTAACGGAGAGGCCAACAGCTGGTCCTCCAGTCCCCAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:75890626..75890718 26863196 MeRIP-seq:(Medium) rs1022593118 Functional Loss SNV dbSNP153 33..33 33 - - - 100418 RMVar_ID_100418 Human_SNP_ID_632984448 m1A Human chr17 - 75894153 75894151 75894153 TGGGGGTCGGTGAGGTGGGAGGACTGAGACAGAGGTGGCTGGAACAGGAGAGGGCACGAAGGCAG TGGGGGTCGGTGAGGTGGGAGGACTGAGACAG__GTGGCTGGAACAGGAGAGGGCACGAAGGCAG CCT C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:75893700..75894635;chr17:75893776..75894626 26863196 MeRIP-seq:(Medium) rs906812833 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2522876,Human_RBP_ID_3541878,Human_RBP_ID_5318584,Human_RBP_ID_6644463,Human_RBP_ID_8189881,Human_RBP_ID_8727479,Human_RBP_ID_9423583,Human_RBP_ID_13165879,Human_RBP_ID_17068197,Human_RBP_ID_18942124,Human_RBP_ID_26782603 100419 RMVar_ID_100419 Human_SNP_ID_632984450 m1A Human chr17 - 75894155 75894154 75894156 GCTGGGGGTCGGTGAGGTGGGAGGACTGAGACAGAGGTGGCTGGAACAGGAGAGGGCACGAAGGC GCTGGGGGTCGGTGAGGTGGGAGGACTGAGA__GAGGTGGCTGGAACAGGAGAGGGCACGAAGGC CTG C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:75893822..75894613;chr17:75893798..75894632 26863196 MeRIP-seq:(Medium) rs1451014501 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3541878,Human_RBP_ID_5318584,Human_RBP_ID_6644463,Human_RBP_ID_8189881,Human_RBP_ID_8727479,Human_RBP_ID_9423583,Human_RBP_ID_13165879,Human_RBP_ID_17068197,Human_RBP_ID_18942124,Human_RBP_ID_25325383,Human_RBP_ID_26782603 100420 RMVar_ID_100420 Human_SNP_ID_632984451 m1A Human chr17 - 75894155 75894155 75894155 GCTGGGGGTCGGTGAGGTGGGAGGACTGAGACAGAGGTGGCTGGAACAGGAGAGGGCACGAAGGC GCTGGGGGTCGGTGAGGTGGGAGGACTGAGACGGAGGTGGCTGGAACAGGAGAGGGCACGAAGGC T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:75893822..75894613;chr17:75893798..75894632 26863196 MeRIP-seq:(Medium) rs59156781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541878,Human_RBP_ID_5318584,Human_RBP_ID_6644463,Human_RBP_ID_8189881,Human_RBP_ID_8727479,Human_RBP_ID_9423583,Human_RBP_ID_13165879,Human_RBP_ID_17068197,Human_RBP_ID_18942124,Human_RBP_ID_25325383,Human_RBP_ID_26782603 100421 RMVar_ID_100421 Human_SNP_ID_632985197 m1A Human chr17 + 75896741 75896689 75896741 GCCCGGCGCGCACCACCTCCAGCACGCCGCTGAGGGCCACGTTGCGGCGCAGCTCGGCGCCGTCG _________________________________GGGCCACGTTGCGGCGCAGCTCGGCGCCGTCG GGGGCCGGGATCCCGGGCGGGCCCGGCGCGCACCACCTCCAGCACGCCGCTGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75896649..75896775 26863196 MeRIP-seq:(Medium) rs1567849034 Functional Loss DEL dbSNP153 1..33 33 - - - 100422 RMVar_ID_100422 Human_SNP_ID_632985225 m1A Human chr17 + 75896741 75896741 75896741 GCCCGGCGCGCACCACCTCCAGCACGCCGCTGAGGGCCACGTTGCGGCGCAGCTCGGCGCCGTCG GCCCGGCGCGCACCACCTCCAGCACGCCGCTGTGGGCCACGTTGCGGCGCAGCTCGGCGCCGTCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75896649..75896775 26863196 MeRIP-seq:(Medium) rs761079116 Functional Loss SNV dbSNP153 33..33 33 - - - 100423 RMVar_ID_100423 Human_SNP_ID_632985901 m1A Human chr17 + 75898756 75898756 75898756 GGAGGGGGCCAAAGAGGGGGGCTGCCTAAGGCAGGGCCCAGACCCCACAGTGTGGGCCTCTGGAG GGAGGGGGCCAAAGAGGGGGGCTGCCTAAGGCCGGGCCCAGACCCCACAGTGTGGGCCTCTGGAG A C AC087289.2 Ensembl:ENSG00000267342 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75898705..75898850 26863196 MeRIP-seq:(Medium) rs910503158 Functional Loss SNV dbSNP153 33..33 33 - - - 100424 RMVar_ID_100424 Human_SNP_ID_632985989 m1A Human chr17 + 75898968 75898968 75898968 TGGGGTGGTAAGGGGGCGGCCGCACGAACTCAAACACCGGCTCCCGCATGTCTGCAAGAAGAGTG TGGGGTGGTAAGGGGGCGGCCGCACGAACTCAGACACCGGCTCCCGCATGTCTGCAAGAAGAGTG A G AC087289.2 Ensembl:ENSG00000267342 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75898741..75899163 32194978 MeRIP-seq:(Medium) rs1486567761 Functional Loss SNV dbSNP153 33..33 33 - - - 100425 RMVar_ID_100425 Human_SNP_ID_632986956 m1A Human chr17 + 75901876 75901876 75901876 CTCAGCCAGACGCTGCTTGTGGTAGGGGCCACAGGTCCTCTCCCACTCGGCCCGCACGGCATCCA CTCAGCCAGACGCTGCTTGTGGTAGGGGCCACGGGTCCTCTCCCACTCGGCCCGCACGGCATCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:75901827..75901935;chr17:75901826..75901934 26863196 MeRIP-seq:(Medium) rs777149219 Functional Loss SNV dbSNP153 33..33 33 - - - 100426 RMVar_ID_100426 Human_SNP_ID_632987093 m1A Human chr17 - 75902147 75902147 75902147 TTTCCCACACATCTTCCCACTCCAGATCCCAAAGAGAAGATTGATATTGGGCTGCCTCCACCCAA TTTCCCACACATCTTCCCACTCCAGATCCCAAGGAGAAGATTGATATTGGGCTGCCTCCACCCAA T C MRPL38,AC087289.3 Ensembl:ENSG00000204316,Ensembl:ENSG00000267426 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75901997..75902146 26863196 MeRIP-seq:(Medium) rs1473097648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896875,Human_RBP_ID_5367920,Human_RBP_ID_13166098,Human_RBP_ID_22544660,Human_RBP_ID_25335925 Human_Splice_Rec_1869578,Human_Splice_Rec_1869624,Human_Splice_Rec_1869634,Human_Splice_Rec_1869638,Human_Splice_Rec_1869644,Human_Splice_Rec_1869652,Human_Splice_Rec_1869660,Human_Splice_Rec_1869666,Human_Splice_Rec_1869682,Human_Splice_Rec_1869742 RMVar_hsa_circ_14083,RMVar_hsa_circ_97784,RMVar_hsa_circ_114087,RMVar_hsa_circ_187116,RMVar_hsa_circ_79852,RMVar_hsa_circ_93982,RMVar_hsa_circ_187117,RMVar_hsa_circ_187118,RMVar_hsa_circ_187115,RMVar_hsa_circ_16266,RMVar_hsa_circ_62723,RMVar_hsa_circ_104568,RMVar_hsa_circ_187119,RMVar_hsa_circ_370636,RMVar_hsa_circ_187120 100427 RMVar_ID_100427 Human_SNP_ID_632987905 m1A Human chr17 + 75904790 75904790 75904790 GCTCGGGCGACAGCCCCCCCCCCCCCCCCCGCAGAGCTGCCCACCCCTCACCCGAGGTGCTGAAG GCTCGGGCGACAGCCCCCCCCCCCCCCCCCGCCGAGCTGCCCACCCCTCACCCGAGGTGCTGAAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75904751..75904875 26863196 MeRIP-seq:(Medium) rs1003344998 Functional Loss SNV dbSNP153 33..33 33 - - - 100428 RMVar_ID_100428 Human_SNP_ID_632987906 m1A Human chr17 + 75904790 75904790 75904790 GCTCGGGCGACAGCCCCCCCCCCCCCCCCCGCAGAGCTGCCCACCCCTCACCCGAGGTGCTGAAG GCTCGGGCGACAGCCCCCCCCCCCCCCCCCGCGGAGCTGCCCACCCCTCACCCGAGGTGCTGAAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:75904751..75904875 26863196 MeRIP-seq:(Medium) rs1003344998 Functional Loss SNV dbSNP153 33..33 33 - - - 100429 RMVar_ID_100429 Human_SNP_ID_632987908 m1A Human chr17 + 75904792 75904792 75904792 TCGGGCGACAGCCCCCCCCCCCCCCCCCGCAGAGCTGCCCACCCCTCACCCGAGGTGCTGAAGCC TCGGGCGACAGCCCCCCCCCCCCCCCCCGCAGCGCTGCCCACCCCTCACCCGAGGTGCTGAAGCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:75904751..75904825 26863196 MeRIP-seq:(Medium) rs1422982279 Functional Loss SNV dbSNP153 33..33 33 - - - 100430 RMVar_ID_100430 Human_SNP_ID_632989944 m1A Human chr17 + 75912202 75912202 75912202 CCCAAGGCCAGGAGAGACTCACCTGCTCTGCCATGTGCCTCAGCAGTGCCAGCCTGGCATGGAGG CCCAAGGCCAGGAGAGACTCACCTGCTCTGCCCTGTGCCTCAGCAGTGCCAGCCTGGCATGGAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75912175..75912259 26863196 MeRIP-seq:(Medium) rs1445475019 Functional Loss SNV dbSNP153 33..33 33 - - - 100431 RMVar_ID_100431 Human_SNP_ID_632992450 m1A Human chr17 + 75920120 75920120 75920120 TCTAGCTCCAGCTTCCGCACCTGGGAGACAGCAGGAGGGCCAGCAACCAGGGAGGGGAGGTGGCT TCTAGCTCCAGCTTCCGCACCTGGGAGACAGCGGGAGGGCCAGCAACCAGGGAGGGGAGGTGGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75920116..75920246 26863196 MeRIP-seq:(Medium) rs1567859677 Functional Loss SNV dbSNP153 33..33 33 - - - 100432 RMVar_ID_100432 Human_SNP_ID_632997420 m1A Human chr17 + 75938095 75938095 75938095 GTGTTGCATGCAGTCAAGATCTTTGGGGATGCAGGATGGGAGGCATGTTCGCTTTCCATGCATCT GTGTTGCATGCAGTCAAGATCTTTGGGGATGCGGGATGGGAGGCATGTTCGCTTTCCATGCATCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75938091..75938277 26863196 MeRIP-seq:(Medium) rs1441117568 Functional Loss SNV dbSNP153 33..33 33 - - - 100433 RMVar_ID_100433 Human_SNP_ID_632998295 m1A Human chr17 + 75940999 75940999 75940999 TGGCTCCATTCGGGTCGCCCAGCCCGGCCAGGACTGGCCTCCCGCTTCCAGCCGCTGCCGGCACC TGGCTCCATTCGGGTCGCCCAGCCCGGCCAGGCCTGGCCTCCCGCTTCCAGCCGCTGCCGGCACC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75940793..75941050 26863196 MeRIP-seq:(Medium) rs191887375 Functional Loss SNV dbSNP153 33..33 33 - - - 100434 RMVar_ID_100434 Human_SNP_ID_633009158 m1A Human chr17 - 75979306 75979306 75979306 TGGCCAGGAGCAGGGGATTAGTCTGCCCCGCGACCGGCCCCAGCCACGACGCGGACATCGCCCCC TGGCCAGGAGCAGGGGATTAGTCTGCCCCGCGCCCGGCCCCAGCCACGACGCGGACATCGCCCCC T G lnc-SRP68-1 RNACentral:URS00008BF89B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:75979282..75979407;chr17:75979276..75979453 26863196 MeRIP-seq:(Medium) rs1031851591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420114 Human_miRNA_ID_2685907 RMVar_hsa_circ_92682,RMVar_hsa_circ_187142 100435 RMVar_ID_100435 Human_SNP_ID_633009163 m1A Human chr17 + 75979317 75979316 75979317 CCGCGTCGTGGCTGGGGCCGGTCGCGGGGCAGACTAATCCCCTGCTCCTGGCCAGGGGAGGCTCC CCGCGTCGTGGCTGGGGCCGGTCGCGGGGCAG_CTAATCCCCTGCTCCTGGCCAGGGGAGGCTCC GA G TEN1,TEN1-CDK3 Ensembl:ENSG00000257949,Ensembl:ENSG00000261408 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75979286..75979407 26863196 MeRIP-seq:(Medium) rs1327712794 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_900807,Human_RBP_ID_4465702,Human_RBP_ID_5581890 100436 RMVar_ID_100436 Human_SNP_ID_633014614 m1A Human chr17 - 76000233 76000233 76000233 TTCCTACTGGCTGCCGCCCCGCTCCTGCTTGTACAGTCTCTGCTCCCGGATGGCTTGTTCCAACA TTCCTACTGGCTGCCGCCCCGCTCCTGCTTGTGCAGTCTCTGCTCCCGGATGGCTTGTTCCAACA T C lnc-SRP68-1 RNACentral:URS00008BF89B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76000201..76000287 26863196 MeRIP-seq:(Medium) rs981085448 Functional Loss SNV dbSNP153 33..33 33 - - - 100437 RMVar_ID_100437 Human_SNP_ID_633014804 m1A Human chr17 + 76000830 76000830 76000830 GGCCGGGCTGAGGCCCTGGGCCCTGACCGTGCAGCCTAAGACAGGACTGTGGCTTTAAGACCCTC GGCCGGGCTGAGGCCCTGGGCCCTGACCGTGCGGCCTAAGACAGGACTGTGGCTTTAAGACCCTC A G TEN1-CDK3 Ensembl:ENSG00000261408 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76000802..76001471 26863196 MeRIP-seq:(Medium) rs948164723 Functional Loss SNV dbSNP153 33..33 33 - - - 100438 RMVar_ID_100438 Human_SNP_ID_633015593 m1A Human chr17 - 76003400 76003400 76003400 GTCGGAGCAGCAGCTGGAGCCCACATGCACCTACCATGAGCAGGTCCCTGCCCTCTGGCTCCAGA GTCGGAGCAGCAGCTGGAGCCCACATGCACCTGCCATGAGCAGGTCCCTGCCCTCTGGCTCCAGA T C lnc-SRP68-1 RNACentral:URS00008BF89B lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76003350..76005399 32194978 MeRIP-seq:(Medium) rs765362129 Functional Loss SNV dbSNP153 33..33 33 - - - 100439 RMVar_ID_100439 Human_SNP_ID_633017759 m1A Human chr17 - 76009241 76009238 76009241 AGACGGTGAGCAAGGAGGTGGTGCGCCACGAGAAGGACCCGGTGCTGGAGAAAGAAGCAGAGCGG AGACGGTGAGCAAGGAGGTGGTGCGCCACGAG___GACCCGGTGCTGGAGAAAGAAGCAGAGCGG CCTT C EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76008285..76010482 26863196 MeRIP-seq:(Medium) rs751406768 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_119593,RMVar_hsa_circ_187149,RMVar_hsa_circ_94567,RMVar_hsa_circ_103978,RMVar_hsa_circ_187151,RMVar_hsa_circ_88770,RMVar_hsa_circ_187150,RMVar_hsa_circ_187147,RMVar_hsa_circ_187148,RMVar_hsa_circ_187146 100440 RMVar_ID_100440 Human_SNP_ID_633017884 m1A Human chr17 - 76009459 76009459 76009459 GGAGGTCCTGCGGGCCCAGAAGCCCACGGTGGAGTACAAGGAGGTGACCCAGGAGGTGGTGAGGC GGAGGTCCTGCGGGCCCAGAAGCCCACGGTGGCGTACAAGGAGGTGACCCAGGAGGTGGTGAGGC T G EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76009428..76009649 26863196 MeRIP-seq:(Medium) rs907576435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2016982,Human_miRNA_ID_2041249 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_119593,RMVar_hsa_circ_187149,RMVar_hsa_circ_94567,RMVar_hsa_circ_103978,RMVar_hsa_circ_187151,RMVar_hsa_circ_88770,RMVar_hsa_circ_187150,RMVar_hsa_circ_187147,RMVar_hsa_circ_187148,RMVar_hsa_circ_187146 100441 RMVar_ID_100441 Human_SNP_ID_633018106 m1A Human chr17 - 76009906 76009906 76009906 CAAGGCAGCCCAGGCTCTGAGGCTGCAGATGGAGGAGGATGCTGCGCGGAGGAAGCAGGCGGAGG CAAGGCAGCCCAGGCTCTGAGGCTGCAGATGGGGGAGGATGCTGCGCGGAGGAAGCAGGCGGAGG T C EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76009677..76010056 26863196 MeRIP-seq:(Medium) rs980355073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376854 Human_miRNA_ID_1938329,Human_miRNA_ID_1949429 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_119593,RMVar_hsa_circ_187149,RMVar_hsa_circ_94567,RMVar_hsa_circ_103978,RMVar_hsa_circ_187151,RMVar_hsa_circ_88770,RMVar_hsa_circ_187150,RMVar_hsa_circ_187147,RMVar_hsa_circ_187148,RMVar_hsa_circ_187146 100442 RMVar_ID_100442 Human_SNP_ID_633020586 m1A Human chr17 - 76017818 76017818 76017818 GCTGGATGGAGACCTGGGACAGATAGAGAGGCAGGTGCTGGCCTGGGCGCGGGCCCCGCTGAGCC GCTGGATGGAGACCTGGGACAGATAGAGAGGCGGGTGCTGGCCTGGGCGCGGGCCCCGCTGAGCC T C EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76017675..76017831 26863196 MeRIP-seq:(Medium) rs779282465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9379006 Human_Splice_Rec_1870350,Human_Splice_Rec_1870351,Human_Splice_Rec_1870392,Human_Splice_Rec_1870393,Human_Splice_Rec_1870431 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_187149,RMVar_hsa_circ_187151,RMVar_hsa_circ_88770,RMVar_hsa_circ_187150 100443 RMVar_ID_100443 Human_SNP_ID_633021749 m1A Human chr17 + 76021513 76021513 76021513 TCCACGTGCTGCAGCTGGGTCTCCTGGCAGATACACAGGTTCAGGAAGTTCTGCCACTCCATCTT TCCACGTGCTGCAGCTGGGTCTCCTGGCAGATGCACAGGTTCAGGAAGTTCTGCCACTCCATCTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76021482..76021566 26863196 MeRIP-seq:(Medium) rs193119748 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 100444 RMVar_ID_100444 Human_SNP_ID_633021904 m1A Human chr17 - 76021705 76021705 76021705 CCAGCTGGAGGACGACGGCGAGCGCATGGTGGAGCTGCGGCACCCCGCGGTGGGGCCCATCCAGG CCAGCTGGAGGACGACGGCGAGCGCATGGTGGCGCTGCGGCACCCCGCGGTGGGGCCCATCCAGG T G EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76021679..76021781 26863196 MeRIP-seq:(Medium) rs761196596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18992377 Human_Splice_Rec_1870338,Human_Splice_Rec_1870339,Human_Splice_Rec_1870380,Human_Splice_Rec_1870381,Human_Splice_Rec_1870422,Human_Splice_Rec_1870423 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_187151,RMVar_hsa_circ_187150 100445 RMVar_ID_100445 Human_SNP_ID_633022234 m1A Human chr17 - 76022395 76022392 76022395 AGCCTCGTGGGGCCGGTAGGTGAGCCTGGAGGATGTCACATCCGGGGCCAGCCCCAGCCCGTTTC AGCCTCGTGGGGCCGGTAGGTGAGCCTGGAGG___TCACATCCGGGGCCAGCCCCAGCCCGTTTC ACAT A EVPL Ensembl:ENSG00000167880 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76022394..76022501 26863196 MeRIP-seq:(Medium) rs1203993579 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_19083999 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_187151,RMVar_hsa_circ_187150 100446 RMVar_ID_100446 Human_SNP_ID_633022563 m1A Human chr17 - 76023374 76023374 76023374 GCACGAGCGGGTGACCCAGGAGTGTGCGGAGTACCGTGCCCTGTACGAGAAGATGGTGCTGCCCC GCACGAGCGGGTGACCCAGGAGTGTGCGGAGTGCCGTGCCCTGTACGAGAAGATGGTGCTGCCCC T C EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76023348..76023505 26863196 MeRIP-seq:(Medium) rs1320110071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1870330,Human_Splice_Rec_1870331,Human_Splice_Rec_1870372,Human_Splice_Rec_1870373,Human_Splice_Rec_1870414,Human_Splice_Rec_1870415 RMVar_hsa_circ_118197,RMVar_hsa_circ_187151 100447 RMVar_ID_100447 Human_SNP_ID_633022623 m1A Human chr17 - 76023504 76023501 76023504 GGCTCAAGCACCCGCAGGCTGAGGAGATTGAGAAGGAGTGAGTGGAGCTGCGGCAGGGCTGGGGG GGCTCAAGCACCCGCAGGCTGAGGAGATTGAG___GAGTGAGTGGAGCTGCGGCAGGGCTGGGGG CCTT C EVPL Ensembl:ENSG00000167880 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76023502..76023605 26863196 MeRIP-seq:(Medium) rs762534558 Functional Loss DEL dbSNP153 33..35 33 - - - Human_Splice_Rec_1870329,Human_Splice_Rec_1870371,Human_Splice_Rec_1870413 RMVar_hsa_circ_118197,RMVar_hsa_circ_187151 100448 RMVar_ID_100448 Human_SNP_ID_633023673 m1A Human chr17 + 76027294 76027294 76027294 TGGGAGGCAGCGGGCGTCCTCACTGGCTGGTCAGCTAAGTCTGGCGAGGTGGGGCGGCTGGGCAC TGGGAGGCAGCGGGCGTCCTCACTGGCTGGTCCGCTAAGTCTGGCGAGGTGGGGCGGCTGGGCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76027243..76027410 26863196 MeRIP-seq:(Medium) rs1200011811 Functional Loss SNV dbSNP153 33..33 33 - - - 100449 RMVar_ID_100449 Human_SNP_ID_633027595 m1A Human chr17 - 76040954 76040954 76040954 TCTTACAGGACCTGCCTGATGTGCAAGAGCTCATCACTCAAGTGCGGTCAGAGAAGTGCTCCCTG TCTTACAGGACCTGCCTGATGTGCAAGAGCTCGTCACTCAAGTGCGGTCAGAGAAGTGCTCCCTG T C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:76040907..76041008 32194978 MeRIP-seq:(Medium) rs1021716893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1542469,Human_RBP_ID_1869317,Human_RBP_ID_3537516,Human_RBP_ID_13166874,Human_RBP_ID_17901075,Human_RBP_ID_18709009,Human_RBP_ID_26812771 Human_Splice_Rec_1870462,Human_Splice_Rec_1870463,Human_Splice_Rec_1870492,Human_Splice_Rec_1870493,Human_Splice_Rec_1870510,Human_Splice_Rec_1870511,Human_Splice_Rec_1870538,Human_Splice_Rec_1870539,Human_Splice_Rec_1870564,Human_Splice_Rec_1870565 RMVar_hsa_circ_60937,RMVar_hsa_circ_121781,RMVar_hsa_circ_187154,RMVar_hsa_circ_92619,RMVar_hsa_circ_187153,RMVar_hsa_circ_378501,RMVar_hsa_circ_108311,RMVar_hsa_circ_187155 100450 RMVar_ID_100450 Human_SNP_ID_633031578 m1A Human chr17 - 76057530 76057530 76057530 TTTTTAAACTATTTTTCAGGCTTTGATCACTCAGACTCGAGCCAAACAGGCAGCTACCATGAGTG TTTTTAAACTATTTTTCAGGCTTTGATCACTCGGACTCGAGCCAAACAGGCAGCTACCATGAGTG T C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:76057396..76060361 32194978 MeRIP-seq:(Medium) rs1273037478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48841,Human_RBP_ID_3951120,Human_RBP_ID_8822365,Human_RBP_ID_9376860,Human_RBP_ID_13167213,Human_RBP_ID_22004489,Human_RBP_ID_26332405 Human_Splice_Rec_1870480,Human_Splice_Rec_1870526,Human_Splice_Rec_1870552,Human_Splice_Rec_1870578 Human_miRNA_ID_632586 RMVar_hsa_circ_10493,RMVar_hsa_circ_34247,RMVar_hsa_circ_121781,RMVar_hsa_circ_187154,RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_71318,RMVar_hsa_circ_70434,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_187159,RMVar_hsa_circ_300113,RMVar_hsa_circ_354689,RMVar_hsa_circ_369297,RMVar_hsa_circ_187158,RMVar_hsa_circ_308428,RMVar_hsa_circ_341208,RMVar_hsa_circ_359897,RMVar_hsa_circ_326868,RMVar_hsa_circ_64674,RMVar_hsa_circ_187160,RMVar_hsa_circ_187161 100451 RMVar_ID_100451 Human_SNP_ID_633036080 m1A Human chr17 - 76072428 76072402 76072429 GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGTAGCGGCGGTGGACGTGGT GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGG___________________________ACGTGGT TCCACCGCCGCTACCGCCGCCGCCACTG T SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76072326..76072478 26863410 MeRIP-seq:(Medium) rs1388970196 Functional Loss DEL dbSNP153 32..58 33 - - - Human_RBP_ID_822100,Human_RBP_ID_3952989,Human_RBP_ID_5115772,Human_RBP_ID_9376864,Human_RBP_ID_26332410 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100452 RMVar_ID_100452 Human_SNP_ID_633036120 m1A Human chr17 - 76072428 76072428 76072428 GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGTAGCGGCGGTGGACGTGGT GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCTGTGGCGGCGGCGGTAGCGGCGGTGGACGTGGT T A SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76072326..76072478 26863410 MeRIP-seq:(Medium) rs377012082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822100,Human_RBP_ID_3952989,Human_RBP_ID_5115772,Human_RBP_ID_9376864,Human_RBP_ID_26332410 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100453 RMVar_ID_100453 Human_SNP_ID_633036121 m1A Human chr17 - 76072428 76072428 76072428 GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGTAGCGGCGGTGGACGTGGT GCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCCGTGGCGGCGGCGGTAGCGGCGGTGGACGTGGT T G SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76072326..76072478 26863410 MeRIP-seq:(Medium) rs377012082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822100,Human_RBP_ID_3952989,Human_RBP_ID_5115772,Human_RBP_ID_9376864,Human_RBP_ID_26332410 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100454 RMVar_ID_100454 Human_SNP_ID_633036136 m1A Human chr17 - 76072446 76072434 76072446 AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGC____________GGTGGCAGTGGCGGCGGCGGT CGCCGCCGCCACT C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:76072390..76072476 26863410 MeRIP-seq:(Medium) rs770467301 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_3952989,Human_RBP_ID_4452227,Human_RBP_ID_5115772,Human_RBP_ID_24373311 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100455 RMVar_ID_100455 Human_SNP_ID_633036159 m1A Human chr17 - 76072446 76072446 76072446 AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCTGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT T A SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:76072390..76072476 26863410 MeRIP-seq:(Medium) rs1041428323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952989,Human_RBP_ID_4452227,Human_RBP_ID_5115772,Human_RBP_ID_24373311 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100456 RMVar_ID_100456 Human_SNP_ID_633036160 m1A Human chr17 - 76072446 76072446 76072446 AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT T C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:76072390..76072476 26863410 MeRIP-seq:(Medium) rs1041428323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952989,Human_RBP_ID_4452227,Human_RBP_ID_5115772,Human_RBP_ID_24373311 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100457 RMVar_ID_100457 Human_SNP_ID_633036184 m1A Human chr17 - 76072468 76072468 76072468 AGGGGCAAGATGGCTGCTGAGAAGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGG AGGGGCAAGATGGCTGCTGAGAAGCAGGTCCCGGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGG T C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:76072315..76072525;chr17:76072369..76072473;chr17:76070376..76072525;chr17:76067276..76072525;chr17:76070390..76072525;chr17:76072327..76072500 26863196,26863410,26863196,26863196,26863196,26863196 MeRIP-seq:(Medium) rs752354929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465703,Human_RBP_ID_24373312 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100458 RMVar_ID_100458 Human_SNP_ID_633036185 m1A Human chr17 - 76072468 76072468 76072468 AGGGGCAAGATGGCTGCTGAGAAGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGG AGGGGCAAGATGGCTGCTGAGAAGCAGGTCCCCGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGG T G SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:76072315..76072525;chr17:76072369..76072473;chr17:76070376..76072525;chr17:76067276..76072525;chr17:76070390..76072525;chr17:76072327..76072500 26863196,26863410,26863196,26863196,26863196,26863196 MeRIP-seq:(Medium) rs752354929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465703,Human_RBP_ID_24373312 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 100459 RMVar_ID_100459 Human_SNP_ID_633036190 m1A Human chr17 + 76072472 76072472 76072472 CGCCACTGCCGCCGCCGCCGCCGCCGCCTGGGACCTGCTTCTCAGCAGCCATCTTGCCCCTGCGC CGCCACTGCCGCCGCCGCCGCCGCCGCCTGGGGCCTGCTTCTCAGCAGCCATCTTGCCCCTGCGC A G ZACN Ensembl:ENSG00000186919 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:76072388..76072472 26863410 MeRIP-seq:(Medium) rs770923950 Functional Loss SNV dbSNP153 33..33 33 - - - 100460 RMVar_ID_100460 Human_SNP_ID_633039728 m1A Human chr17 + 76081690 76081690 76081690 CATAGGCTACAAGGTGACATTGCTGCTGAGTTACCTCGTCCTCCACTCCTCCCTGGTGCAGGCCC CATAGGCTACAAGGTGACATTGCTGCTGAGTTTCCTCGTCCTCCACTCCTCCCTGGTGCAGGCCC A T ZACN Ensembl:ENSG00000186919 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76081640..76081816 26863196 MeRIP-seq:(Medium) rs1479548159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1870611,Human_Splice_Rec_1870627,Human_Splice_Rec_1870638,Human_Splice_Rec_1870639 100461 RMVar_ID_100461 Human_SNP_ID_633040265 m1A Human chr17 - 76083260 76083260 76083260 CTAGGTCAGAGGTGGGGACAGAGAACTCCCCTACAGCCCAGAGATGTGGCAGGGCTCAGAGAAGC CTAGGTCAGAGGTGGGGACAGAGAACTCCCCTCCAGCCCAGAGATGTGGCAGGGCTCAGAGAAGC T G EXOC7 Ensembl:ENSG00000182473 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76083213..76083314 32194978 MeRIP-seq:(Medium) rs981124099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820258,Human_RBP_ID_4452304,Human_RBP_ID_13167613 RMVar_hsa_circ_78018,RMVar_hsa_circ_187168 100462 RMVar_ID_100462 Human_SNP_ID_633040266 m1A Human chr17 + 76083261 76083261 76083261 CTTCTCTGAGCCCTGCCACATCTCTGGGCTGTAGGGGAGTTCTCTGTCCCCACCTCTGACCTAGG CTTCTCTGAGCCCTGCCACATCTCTGGGCTGTGGGGGAGTTCTCTGTCCCCACCTCTGACCTAGG A G ZACN Ensembl:ENSG00000186919 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:76083213..76083314 32194978 MeRIP-seq:(Medium) rs927886022 Functional Loss SNV dbSNP153 33..33 33 - - - 100463 RMVar_ID_100463 Human_SNP_ID_633044522 m1A Human chr17 - 76097832 76097832 76097832 TGCCCGAGAGCGTGCTCCAGGATGTCATTCGCATCTCCCGCTGGCTGGTGGAATATGGCCGCAAC TGCCCGAGAGCGTGCTCCAGGATGTCATTCGCGTCTCCCGCTGGCTGGTGGAATATGGCCGCAAC T C EXOC7 Ensembl:ENSG00000182473 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:76094569..76097934 32194978 MeRIP-seq:(Medium) rs1048616996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49462,Human_RBP_ID_9376879,Human_RBP_ID_17901132,Human_RBP_ID_18992407 Human_Splice_Rec_1870653,Human_Splice_Rec_1870691,Human_Splice_Rec_1870729,Human_Splice_Rec_1870767,Human_Splice_Rec_1870803,Human_Splice_Rec_1870841,Human_Splice_Rec_1870891,Human_Splice_Rec_1870925,Human_Splice_Rec_1870963,Human_Splice_Rec_1871027,Human_Splice_Rec_1871033 RMVar_hsa_circ_187171,RMVar_hsa_circ_94043,RMVar_hsa_circ_187170,RMVar_hsa_circ_376262,RMVar_hsa_circ_38134,RMVar_hsa_circ_187174,RMVar_hsa_circ_281941,RMVar_hsa_circ_325729,RMVar_hsa_circ_187175,RMVar_hsa_circ_276179,RMVar_hsa_circ_291650,RMVar_hsa_circ_187176,RMVar_hsa_circ_187177 100464 RMVar_ID_100464 Human_SNP_ID_633046150 m1A Human chr17 - 76103425 76103425 76103425 CTGGTGATGTCCTCCCCTTGCCTGCCCCCAGGAGGAGGAGACTCTGTCCTTCATCCGAGACAGCC CTGGTGATGTCCTCCCCTTGCCTGCCCCCAGGGGGAGGAGACTCTGTCCTTCATCCGAGACAGCC T C EXOC7 Ensembl:ENSG00000182473 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76103408..76103483 26863196 MeRIP-seq:(Medium) rs1240066492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896885,Human_RBP_ID_5114867,Human_RBP_ID_5367969,Human_RBP_ID_9376883,Human_RBP_ID_18420115,Human_RBP_ID_18992412,Human_RBP_ID_19080106,Human_RBP_ID_26333846 Human_Splice_Rec_1870646,Human_Splice_Rec_1870647,Human_Splice_Rec_1870684,Human_Splice_Rec_1870685,Human_Splice_Rec_1870722,Human_Splice_Rec_1870723,Human_Splice_Rec_1870760,Human_Splice_Rec_1870761,Human_Splice_Rec_1870797,Human_Splice_Rec_1870834,Human_Splice_Rec_1870835,Human_Splice_Rec_1870918,Human_Splice_Rec_1870919,Human_Splice_Rec_1870956,Human_Splice_Rec_1870957,Human_Splice_Rec_1871020,Human_Splice_Rec_1871021,Human_Splice_Rec_1871048,Human_Splice_Rec_1871049,Human_Splice_Rec_1871056,Human_Splice_Rec_1871057 RMVar_hsa_circ_38134 100465 RMVar_ID_100465 Human_SNP_ID_633046262 m1A Human chr17 + 76103691 76103691 76103691 GCCGTCGAGCGGATGCCTCCTGTGGGGGAATCATCGCTCTGAACCCCGCGGCTCCCACTCCCCAG GCCGTCGAGCGGATGCCTCCTGTGGGGGAATCTTCGCTCTGAACCCCGCGGCTCCCACTCCCCAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76103437..76103750 26863196 MeRIP-seq:(Medium) rs750592881 Functional Loss SNV dbSNP153 33..33 33 - - - 100466 RMVar_ID_100466 Human_SNP_ID_633089346 m1A Human chr17 + 76265376 76265361 76265376 AACCACAACATTCGCCGGGCGGGCGGCGGCGGAGCGGGCGGCGGAGCGGCGGCAGCAGCGGTGAG AACCACAACATTCGCCGG_______________GCGGGCGGCGGAGCGGCGGCAGCAGCGGTGAG GGCGGGCGGCGGCGGA G UBALD2 Ensembl:ENSG00000185262 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:76265326..76265650;chr17:76265326..76265550 26863196 MeRIP-seq:(Medium) rs1251658289 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_238257,Human_RBP_ID_767542,Human_RBP_ID_4464796,Human_RBP_ID_9326840,Human_RBP_ID_17378543 Human_Splice_Rec_1871241 100467 RMVar_ID_100467 Human_SNP_ID_633089357 m1A Human chr17 + 76265376 76265376 76265376 AACCACAACATTCGCCGGGCGGGCGGCGGCGGAGCGGGCGGCGGAGCGGCGGCAGCAGCGGTGAG AACCACAACATTCGCCGGGCGGGCGGCGGCGGGGCGGGCGGCGGAGCGGCGGCAGCAGCGGTGAG A G UBALD2 Ensembl:ENSG00000185262 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:76265326..76265650;chr17:76265326..76265550 26863196 MeRIP-seq:(Medium) rs1480897036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238257,Human_RBP_ID_767542,Human_RBP_ID_4464796,Human_RBP_ID_9326840,Human_RBP_ID_17378543 Human_Splice_Rec_1871241 100468 RMVar_ID_100468 Human_SNP_ID_633089384 m1A Human chr17 + 76265453 76265453 76265453 AGCCCCGGGCGGCCGGCCTCCCGCGCCCGCGCAGCCCCGCGTCTGCGTCCGGCCGGAGACGCCGG AGCCCCGGGCGGCCGGCCTCCCGCGCCCGCGCGGCCCCGCGTCTGCGTCCGGCCGGAGACGCCGG A G UBALD2 Ensembl:ENSG00000185262 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:76265351..76265501 26863410 MeRIP-seq:(Medium) rs1359323313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464797,Human_RBP_ID_5237938,Human_RBP_ID_8825728,Human_RBP_ID_8941849 100469 RMVar_ID_100469 Human_SNP_ID_633089433 m1A Human chr17 - 76265558 76265558 76265558 TCGCCTGGTCGGCCGCGCAGCCCGCGGCCAGCACGAACTGGTTGATCATGACCTGGTGCCGCAGC TCGCCTGGTCGGCCGCGCAGCCCGCGGCCAGCGCGAACTGGTTGATCATGACCTGGTGCCGCAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:76265373..76265659 26863196 MeRIP-seq:(Medium) rs1279184044 Functional Loss SNV dbSNP153 33..33 33 - - - 100470 RMVar_ID_100470 Human_SNP_ID_633090930 m1A Human chr17 + 76270296 76270296 76270296 TCCGCGCCTCCGAGGGCCTGCAGAGCAGCAACAGCCCCATGACAGCCGCAGCCTGCTCCCCACCT TCCGCGCCTCCGAGGGCCTGCAGAGCAGCAACGGCCCCATGACAGCCGCAGCCTGCTCCCCACCT A G UBALD2 Ensembl:ENSG00000185262 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:76265926..76270451 26863196 MeRIP-seq:(Medium) rs774980074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17264165,Human_RBP_ID_17378544,Human_RBP_ID_26333851 RMVar_hsa_circ_101718,RMVar_hsa_circ_187185 100471 RMVar_ID_100471 Human_SNP_ID_633090941 m1A Human chr17 - 76270320 76270320 76270320 GGCCCAGAAGGGGCTGAAGTTTGCAGGTGGGGAGCAGGCTGCGGCTGTCATGGGGCTGTTGCTGC GGCCCAGAAGGGGCTGAAGTTTGCAGGTGGGGGGCAGGCTGCGGCTGTCATGGGGCTGTTGCTGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76270165..76270400 26863410 MeRIP-seq:(Medium) rs1484030959 Functional Loss SNV dbSNP153 33..33 33 - - - 100472 RMVar_ID_100472 Human_SNP_ID_633093300 m1A Human chr17 + 76277764 76277763 76277765 ACTCACTCCCACACTCATACACACACGCACTCATACACACACACCCTTACACACACTCATACATT ACTCACTCCCACACTCATACACACACGCACTC__ACACACACACCCTTACACACACTCATACATT CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76277757..76277845 26863196 MeRIP-seq:(Medium) rs926475743 Functional Loss DEL dbSNP153 33..34 33 - - - 100473 RMVar_ID_100473 Human_SNP_ID_633114122 m1A Human chr17 - 76348583 76348583 76348583 TTAATTTCCCTTTTTTGTTCTTTTTGATCTATAGGCGCCTTGGTGCTGAATTGGGGAAGTCTGTT TTAATTTCCCTTTTTTGTTCTTTTTGATCTATGGGCGCCTTGGTGCTGAATTGGGGAAGTCTGTT T C PRPSAP1 Ensembl:ENSG00000161542 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76348551..76348600 26863196 MeRIP-seq:(Medium) rs746648535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4479142,Human_RBP_ID_25337366 Human_Splice_Rec_1871391,Human_Splice_Rec_1871409,Human_Splice_Rec_1871435,Human_Splice_Rec_1871457,Human_Splice_Rec_1871469,Human_Splice_Rec_1871477,Human_Splice_Rec_1871485 100474 RMVar_ID_100474 Human_SNP_ID_633115647 m1A Human chr17 - 76353613 76353613 76353613 CGCGCGCCCGCCCCGTTCCCCCGCCGGCCATGAACGCCGCTCGCACCGGCTACCGAGTCTTCTCG CGCGCGCCCGCCCCGTTCCCCCGCCGGCCATGGACGCCGCTCGCACCGGCTACCGAGTCTTCTCG T C PRPSAP1 Ensembl:ENSG00000161542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76353563..76353863 26863196 MeRIP-seq:(Medium) rs1244371799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1871389,Human_Splice_Rec_1871467 100475 RMVar_ID_100475 Human_SNP_ID_633124229 m1A Human chr17 + 76384717 76384717 76384717 GTCCGCTCCAGCGGGGCGCTCCAGTCCCTCAGACGTGGGCTGAGCTTGGGACGAGCTGCGTTCCG GTCCGCTCCAGCGGGGCGCTCCAGTCCCTCAGGCGTGGGCTGAGCTTGGGACGAGCTGCGTTCCG A G SPHK1 Ensembl:ENSG00000176170 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76384672..76384762 26863196 MeRIP-seq:(Medium) rs1458800349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3545727,Human_RBP_ID_4452701,Human_RBP_ID_9327457,Human_RBP_ID_17654936,Human_RBP_ID_18419738,Human_RBP_ID_22959675 Human_Splice_Rec_1871535,Human_Splice_Rec_1871545 100476 RMVar_ID_100476 Human_SNP_ID_633125217 m1A Human chr17 + 76386958 76386958 76386958 TGTGCTCAGCCTGGCCTGGGGCTTCATTGCTGATGTGGACCTAGAGAGTGAGAAGTATCGGCGTC TGTGCTCAGCCTGGCCTGGGGCTTCATTGCTGTTGTGGACCTAGAGAGTGAGAAGTATCGGCGTC A T SPHK1 Ensembl:ENSG00000176170 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76385845..76387375 32194978 MeRIP-seq:(Medium) rs1407687659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8463578,Human_RBP_ID_17905583 100477 RMVar_ID_100477 Human_SNP_ID_633128396 m1A Human chr17 - 76396677 76396677 76396677 CGGACAATGGGCTGGTGGAGGACGAGCACCCCAAGATAGAGGAGCCCCCCATCCCACCCCTGGAG CGGACAATGGGCTGGTGGAGGACGAGCACCCCCAGATAGAGGAGCCCCCCATCCCACCCCTGGAG T G UBE2O Ensembl:ENSG00000175931 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76396626..76396825 26863196 MeRIP-seq:(Medium) rs1296668475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6645205,Human_RBP_ID_9289370,Human_RBP_ID_18412079,Human_RBP_ID_18470118,Human_RBP_ID_18709255,Human_RBP_ID_26332428 RMVar_hsa_circ_187207,RMVar_hsa_circ_117014,RMVar_hsa_circ_124428,RMVar_hsa_circ_107553,RMVar_hsa_circ_88725,RMVar_hsa_circ_92965,RMVar_hsa_circ_87493,RMVar_hsa_circ_187211,RMVar_hsa_circ_79710,RMVar_hsa_circ_83791,RMVar_hsa_circ_187213,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_26045,RMVar_hsa_circ_187206,RMVar_hsa_circ_12448,RMVar_hsa_circ_353741,RMVar_hsa_circ_67135 100478 RMVar_ID_100478 Human_SNP_ID_633143335 m1A Human chr17 - 76452813 76452813 76452813 GGGGTGCTCCGAGGCCGGGGGCGCGGGCCACGAGGAGGGCCGGGCCAGCCCCCTGCGCCGCGGCT GGGGTGCTCCGAGGCCGGGGGCGCGGGCCACGGGGAGGGCCGGGCCAGCCCCCTGCGCCGCGGCT T C UBE2O Ensembl:ENSG00000175931 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:76452767..76452888 26863196 MeRIP-seq:(Medium) rs1221005850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9290323,Human_RBP_ID_9327461 Human_Splice_Rec_1871575,Human_Splice_Rec_1871623 100479 RMVar_ID_100479 Human_SNP_ID_633143398 m1A Human chr17 + 76452976 76452976 76452976 CACCAGGTCGTGAGAAAACAGCAGGCGCTGCGAGCCGGCTTCTGGGCCGGAGTCCGAGGACGGCC CACCAGGTCGTGAGAAAACAGCAGGCGCTGCGCGCCGGCTTCTGGGCCGGAGTCCGAGGACGGCC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:76452926..76453150 26863196 MeRIP-seq:(Medium) rs1315806057 Functional Loss SNV dbSNP153 33..33 33 - - - 100480 RMVar_ID_100480 Human_SNP_ID_633148596 m1A Human chr17 + 76471784 76471784 76471784 CGGCGAAGAGGCCGGCAAAGGCCAGCAGTGACACCAGGATGAGTGCCCGCTTGCGGTACTTGTCG CGGCGAAGAGGCCGGCAAAGGCCAGCAGTGACGCCAGGATGAGTGCCCGCTTGCGGTACTTGTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76471733..76471868 26863196 MeRIP-seq:(Medium) rs937545016 Functional Loss SNV dbSNP153 33..33 33 - - - 100481 RMVar_ID_100481 Human_SNP_ID_633149964 m1A Human chr17 - 76475436 76475436 76475436 GGCCCTGGGGCTGGAAGGGCAAAGTACATCCCAGGAAATGCAGGCAAAGAGGCCAGAGAGGTGGT GGCCCTGGGGCTGGAAGGGCAAAGTACATCCCGGGAAATGCAGGCAAAGAGGCCAGAGAGGTGGT T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76475434..76475512 26863196 MeRIP-seq:(Medium) rs1356332386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187224,RMVar_hsa_circ_106548 100482 RMVar_ID_100482 Human_SNP_ID_633153005 m1A Human chr17 - 76484468 76484468 76484468 GTGGAGGTGAGGTAGAGATGGAGGAGGAGGACAGGTTCAGATGGCTGCTGTCTCGCCGACCCGTG GTGGAGGTGAGGTAGAGATGGAGGAGGAGGACGGGTTCAGATGGCTGCTGTCTCGCCGACCCGTG T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76484466..76484755 26863196 MeRIP-seq:(Medium) rs987725834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 100483 RMVar_ID_100483 Human_SNP_ID_633153013 m1A Human chr17 - 76484487 76484487 76484487 TGGAGGTGAGGTGGAGATGGTGGAGGTGAGGTAGAGATGGAGGAGGAGGACAGGTTCAGATGGCT TGGAGGTGAGGTGGAGATGGTGGAGGTGAGGTGGAGATGGAGGAGGAGGACAGGTTCAGATGGCT T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76484484..76484679 26863196 MeRIP-seq:(Medium) rs1186440404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 100484 RMVar_ID_100484 Human_SNP_ID_633153037 m1A Human chr17 - 76484570 76484570 76484570 CGGAGAATGATCAGTCTCAGGGGGCTTGAGGCAGCAGGTAGAGGAATTGAGAGAGTGGAGTGAGC CGGAGAATGATCAGTCTCAGGGGGCTTGAGGCGGCAGGTAGAGGAATTGAGAGAGTGGAGTGAGC T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76484436..76484745 26863196 MeRIP-seq:(Medium) rs560142722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 100485 RMVar_ID_100485 Human_SNP_ID_633157672 m1A Human chr17 + 76501181 76501181 76501181 CGCCGGCGCCGTCTGAGCCAGCCCGGGCCTCCAGCCGAGCCCACGTGGGACCCAGGCGCTCCGCA CGCCGGCGCCGTCTGAGCCAGCCCGGGCCTCCGGCCGAGCCCACGTGGGACCCAGGCGCTCCGCA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:76501146..76501278 26863196 MeRIP-seq:(Medium) rs958790666 Functional Loss SNV dbSNP153 33..33 33 - - - 100486 RMVar_ID_100486 Human_SNP_ID_633173667 m1A Human chr17 - 76557248 76557248 76557248 GCGAGGCCGGTGAAGCCGAGGCGCGGGCGGCAAGGAGCGCTGGAGAGCGACGGGGCTCGGCCTCC GCGAGGCCGGTGAAGCCGAGGCGCGGGCGGCAGGGAGCGCTGGAGAGCGACGGGGCTCGGCCTCC T C AC015802.4 Ensembl:ENSG00000267546 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76557197..76557350 26863196 MeRIP-seq:(Medium) rs1451426074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1871990 100487 RMVar_ID_100487 Human_SNP_ID_633182204 m1A Human chr17 - 76585908 76585908 76585908 GCGCCGCAGGCACCCGGCGGGCAGGGCGGGGCAGGGCAAGACGGCCGCCTCCGCAAGTGCCACCC GCGCCGCAGGCACCCGGCGGGCAGGGCGGGGCGGGGCAAGACGGCCGCCTCCGCAAGTGCCACCC T C ST6GALNAC2 Ensembl:ENSG00000070731 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76585900..76586022 26863196 MeRIP-seq:(Medium) rs537049576 Functional Loss SNV dbSNP153 33..33 33 - - - 100488 RMVar_ID_100488 Human_SNP_ID_633208817 m1A Human chr17 + 76683814 76683814 76683814 TTTGGGGGCACGTTAGCACGCAGTAGAAGGGGAGCACCACTAGTCTAAGAAATCAGTGTCCTTAC TTTGGGGGCACGTTAGCACGCAGTAGAAGGGGGGCACCACTAGTCTAAGAAATCAGTGTCCTTAC A G SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76683811..76683976 26863196 MeRIP-seq:(Medium) rs1357565142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8463869,Human_RBP_ID_13174289 100489 RMVar_ID_100489 Human_SNP_ID_633216453 m1A Human chr17 - 76710930 76710930 76710930 CGGCGGCCGCGGCGCGATGGAGGCGCCGGCCGAGCTACTGGCCGCGCTGCCTGCGCTGGCCACCG CGGCGGCCGCGGCGCGATGGAGGCGCCGGCCGGGCTACTGGCCGCGCTGCCTGCGCTGGCCACCG T C MXRA7 Ensembl:ENSG00000182534 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76710886..76710996 26863196 MeRIP-seq:(Medium) rs1249467688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238245,Human_RBP_ID_500707,Human_RBP_ID_4465715 100490 RMVar_ID_100490 Human_SNP_ID_633218608 m1A Human chr17 - 76718669 76718669 76718669 GGACACGCTCGCGGCAAGGGCAGGGCCTGGGGAGGGTGGCCTGTCCAGTCCTGCAGACAAGGGGA GGACACGCTCGCGGCAAGGGCAGGGCCTGGGGCGGGTGGCCTGTCCAGTCCTGCAGACAAGGGGA T G JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76718619..76718887 26863196 MeRIP-seq:(Medium) rs1255355987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4453193,Human_RBP_ID_5115256,Human_RBP_ID_5497858,Human_RBP_ID_17654940,Human_RBP_ID_26332435 100491 RMVar_ID_100491 Human_SNP_ID_633218615 m1A Human chr17 - 76718680 76718680 76718680 TCTGTATGGAAGGACACGCTCGCGGCAAGGGCAGGGCCTGGGGAGGGTGGCCTGTCCAGTCCTGC TCTGTATGGAAGGACACGCTCGCGGCAAGGGCGGGGCCTGGGGAGGGTGGCCTGTCCAGTCCTGC T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:76718633..76718859;chr17:76718632..76718802 26863196 MeRIP-seq:(Medium) rs776217581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5497858,Human_RBP_ID_17654940 100492 RMVar_ID_100492 Human_SNP_ID_633221426 m1A Human chr17 - 76726881 76726881 76726881 GAAGAAAGCCCGGAGCAAGGCGAAAGAGACTCACACGCGCAGAACTGGCAACGGGCGGCTGGCGC GAAGAAAGCCCGGAGCAAGGCGAAAGAGACTCCCACGCGCAGAACTGGCAACGGGCGGCTGGCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76726851..76727050 26863196 MeRIP-seq:(Medium) rs1568005516 Functional Loss SNV dbSNP153 33..33 33 - - - 100493 RMVar_ID_100493 Human_SNP_ID_633224587 m1A Human chr17 - 76736245 76736245 76736245 AGGTCCCGGTCTCGGTCCAGGAGTCCTCCCCCAGTGTCCAAGAGGGAATCCAAATCCAGGTCGCG AGGTCCCGGTCTCGGTCCAGGAGTCCTCCCCCCGTGTCCAAGAGGGAATCCAAATCCAGGTCGCG T G SRSF2 Ensembl:ENSG00000161547 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:76736175..76736900 26863196 MeRIP-seq:(Medium) rs1283104650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48773,Human_RBP_ID_500797,Human_RBP_ID_821284,Human_RBP_ID_903694,Human_RBP_ID_1010718,Human_RBP_ID_1543077,Human_RBP_ID_3537950,Human_RBP_ID_4479323,Human_RBP_ID_6646654,Human_RBP_ID_9376907,Human_RBP_ID_13175181,Human_RBP_ID_17901445,Human_RBP_ID_22059663,Human_RBP_ID_22806954,Human_RBP_ID_25326902,Human_RBP_ID_26330892,Human_RBP_ID_26972184,Human_RBP_ID_27260279 Human_Splice_Rec_1872427,Human_Splice_Rec_1872433,Human_Splice_Rec_1872437,Human_Splice_Rec_1872445,Human_Splice_Rec_1872457 Human_miRNA_ID_2956442 RMVar_hsa_circ_187247,RMVar_hsa_circ_114043,RMVar_hsa_circ_90518,RMVar_hsa_circ_187246 100494 RMVar_ID_100494 Human_SNP_ID_633224937 m1A Human chr17 - 76736813 76736813 76736813 CCACCCCGCAGGTACGGGGGCGGTGGCTACGGACGCCGGAGCCGCAGGTAAACGGGGCTGAGGGG CCACCCCGCAGGTACGGGGGCGGTGGCTACGGGCGCCGGAGCCGCAGGTAAACGGGGCTGAGGGG T C SRSF2 Ensembl:ENSG00000161547 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76736795..76736893 26863196 MeRIP-seq:(Medium) rs1234366669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903696,Human_RBP_ID_1010722,Human_RBP_ID_4479333,Human_RBP_ID_5497865,Human_RBP_ID_6646666,Human_RBP_ID_18439732,Human_RBP_ID_22443912,Human_RBP_ID_27838538 Human_Splice_Rec_1872425,Human_Splice_Rec_1872429,Human_Splice_Rec_1872431,Human_Splice_Rec_1872443,Human_Splice_Rec_1872463 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 100495 RMVar_ID_100495 Human_SNP_ID_633224953 m1A Human chr17 - 76736849 76736849 76736849 CGCCCCCCGGACTCACACCACAGCCGCCGGGGACCGCCACCCCGCAGGTACGGGGGCGGTGGCTA CGCCCCCCGGACTCACACCACAGCCGCCGGGGGCCGCCACCCCGCAGGTACGGGGGCGGTGGCTA T C SRSF2 Ensembl:ENSG00000161547 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:76736751..76736900 26863196 MeRIP-seq:(Medium) rs932978794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22443912,Human_RBP_ID_22586955 Human_Splice_Rec_1872425,Human_Splice_Rec_1872429,Human_Splice_Rec_1872431,Human_Splice_Rec_1872443,Human_Splice_Rec_1872455,Human_Splice_Rec_1872461,Human_Splice_Rec_1872463 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 100496 RMVar_ID_100496 Human_SNP_ID_633225061 m1A Human chr17 + 76737154 76737154 76737154 CATACCCTCCACATCGGGAGGGGGGCGGCCGTAGCTCATAGCTCTGAGTGGCGGCCCGGAGCCCC CATACCCTCCACATCGGGAGGGGGGCGGCCGTGGCTCATAGCTCTGAGTGGCGGCCCGGAGCCCC A G AC005837.2,MFSD11 Ensembl:ENSG00000267168,Ensembl:ENSG00000092931 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:76736776..76737300 32194978 MeRIP-seq:(Medium) rs1474816451 Functional Loss SNV dbSNP153 33..33 33 - - - 100497 RMVar_ID_100497 Human_SNP_ID_633225071 m1A Human chr17 - 76737170 76737170 76737170 GCCGGCGCCAGTTCGCGGGGCTCCGGGCCGCCACTCAGAGCTATGAGCTACGGCCGCCCCCCTCC GCCGGCGCCAGTTCGCGGGGCTCCGGGCCGCCGCTCAGAGCTATGAGCTACGGCCGCCCCCCTCC T C SRSF2 Ensembl:ENSG00000161547 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76737076..76737325 26863410 MeRIP-seq:(Medium) rs1368260265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1010728,Human_RBP_ID_1543091,Human_RBP_ID_4479352,Human_RBP_ID_6666241,Human_RBP_ID_8463968,Human_RBP_ID_18419741,Human_RBP_ID_18709584,Human_RBP_ID_22443913,Human_RBP_ID_22500525,Human_RBP_ID_23750908,Human_RBP_ID_27669738 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 100498 RMVar_ID_100498 Human_SNP_ID_633225072 m1A Human chr17 - 76737170 76737170 76737170 GCCGGCGCCAGTTCGCGGGGCTCCGGGCCGCCACTCAGAGCTATGAGCTACGGCCGCCCCCCTCC GCCGGCGCCAGTTCGCGGGGCTCCGGGCCGCCCCTCAGAGCTATGAGCTACGGCCGCCCCCCTCC T G SRSF2 Ensembl:ENSG00000161547 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76737076..76737325 26863410 MeRIP-seq:(Medium) rs1368260265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1010728,Human_RBP_ID_1543091,Human_RBP_ID_4479352,Human_RBP_ID_6666241,Human_RBP_ID_8463968,Human_RBP_ID_18419741,Human_RBP_ID_18709584,Human_RBP_ID_22443913,Human_RBP_ID_22500525,Human_RBP_ID_23750908,Human_RBP_ID_27669738 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 100499 RMVar_ID_100499 Human_SNP_ID_633225190 m1A Human chr17 - 76737302 76737302 76737302 CCCAGTTGTTACTCAGGTGCGCTAGCCTGCGGAGCCCGTCCGTGCTGTTCTGCGGCAAGGCCTTT CCCAGTTGTTACTCAGGTGCGCTAGCCTGCGGGGCCCGTCCGTGCTGTTCTGCGGCAAGGCCTTT T C SRSF2 Ensembl:ENSG00000161547 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:76737301..76737325 26863196 MeRIP-seq:(Medium) rs1259514308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48775,Human_RBP_ID_236547,Human_RBP_ID_278644,Human_RBP_ID_500813,Human_RBP_ID_821287,Human_RBP_ID_1010729,Human_RBP_ID_1543092,Human_RBP_ID_4465726,Human_RBP_ID_5318592,Human_RBP_ID_5420528,Human_RBP_ID_5441944,Human_RBP_ID_5467064,Human_RBP_ID_5497866,Human_RBP_ID_6646672,Human_RBP_ID_8463971,Human_RBP_ID_8825739,Human_RBP_ID_9327467,Human_RBP_ID_9379094,Human_RBP_ID_13175220,Human_RBP_ID_18419743,Human_RBP_ID_18709586,Human_RBP_ID_18989330,Human_RBP_ID_22061683,Human_RBP_ID_22221808,Human_RBP_ID_22443191,Human_RBP_ID_22532988,Human_RBP_ID_23210122,Human_RBP_ID_23750910,Human_RBP_ID_27457458 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 100500 RMVar_ID_100500 Human_SNP_ID_633261118 m1A Human chr17 + 76868498 76868498 76868498 ACGCCGGACACCAGAGCGCGGGCGGCGGAGCCAGCGGGCGAGAGAGCGCGCGGCGGGCGCGGGTT ACGCCGGACACCAGAGCGCGGGCGGCGGAGCCGGCGGGCGAGAGAGCGCGCGGCGGGCGCGGGTT A G MGAT5B Ensembl:ENSG00000167889 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:76868472..76868706 26863196 MeRIP-seq:(Medium) rs1166051769 Functional Loss SNV dbSNP153 33..33 33 - - - 100501 RMVar_ID_100501 Human_SNP_ID_633261225 m1A Human chr17 + 76868844 76868844 76868844 GGCCCGGCCGGGCGCCCTCGCCGCCCTCCGGCAGCCGCGCCGCTCCCTCCGCTGCACGCCCAGGC GGCCCGGCCGGGCGCCCTCGCCGCCCTCCGGCGGCCGCGCCGCTCCCTCCGCTGCACGCCCAGGC A G MGAT5B Ensembl:ENSG00000167889 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:76868803..76868933 26863196 MeRIP-seq:(Medium) rs1203660451 Functional Loss SNV dbSNP153 33..33 33 - - - 100502 RMVar_ID_100502 Human_SNP_ID_633262282 m1A Human chr17 + 76872766 76872766 76872766 CTTGCTTCCTTCACTCATGCACTCATTCGTAAAACATTTGTGCAGCCGGTACGTGGTGGAGCGTC CTTGCTTCCTTCACTCATGCACTCATTCGTAAGACATTTGTGCAGCCGGTACGTGGTGGAGCGTC A G MGAT5B Ensembl:ENSG00000167889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76872764..76872854 26863196 MeRIP-seq:(Medium) rs1034955603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125395,RMVar_hsa_circ_187270 100503 RMVar_ID_100503 Human_SNP_ID_633264695 m1A Human chr17 - 76882223 76882223 76882223 CACTGCTGTTCTCCAGCCTGGCCAGTGCGTCCATGCGCTTCACCATCAGCTCCAGCAGGTCGCTC CACTGCTGTTCTCCAGCCTGGCCAGTGCGTCCGTGCGCTTCACCATCAGCTCCAGCAGGTCGCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76872852..76882377 32194978 MeRIP-seq:(Medium) rs773193132 Functional Loss SNV dbSNP153 33..33 33 - - - 100504 RMVar_ID_100504 Human_SNP_ID_633272935 m1A Human chr17 + 76913629 76913629 76913629 TGTCAAAGGATGGGAAAACAGGCTTGAGGGGCACAGACTTGGGAAATATCAACACAGAAAGGCCT TGTCAAAGGATGGGAAAACAGGCTTGAGGGGCGCAGACTTGGGAAATATCAACACAGAAAGGCCT A G MGAT5B Ensembl:ENSG00000167889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:76913616..76913745 26863196 MeRIP-seq:(Medium) rs750164869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125395,RMVar_hsa_circ_187270,RMVar_hsa_circ_106333,RMVar_hsa_circ_187272 100505 RMVar_ID_100505 Human_SNP_ID_633277799 m1A Human chr17 - 76931513 76931512 76931513 TCCATACAGAACTGTGCTCATGGGCCTGTGAGAGGTCTCTCCTGACCCCAGTCACTCATTGTCCC TCCATACAGAACTGTGCTCATGGGCCTGTGAG_GGTCTCTCCTGACCCCAGTCACTCATTGTCCC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76931506..76931615 26863196 MeRIP-seq:(Medium) rs1331529563 Functional Loss DEL dbSNP153 33..33 33 - - - 100506 RMVar_ID_100506 Human_SNP_ID_633279573 m1A Human chr17 + 76937485 76937485 76937485 GGGTGAATGGATGGATGGGTGGGTGGACGCATAGAGTTATGGGCAGGTGGACAAATGGATGGATG GGGTGAATGGATGGATGGGTGGGTGGACGCATGGAGTTATGGGCAGGTGGACAAATGGATGGATG A G MGAT5B Ensembl:ENSG00000167889 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76937377..76937638 26863196 MeRIP-seq:(Medium) rs771980365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187273,RMVar_hsa_circ_341162 100507 RMVar_ID_100507 Human_SNP_ID_633280401 m1A Human chr17 + 76940453 76940453 76940453 TCCCCTACGAGGGCCCCGCCCCCCTGGAGGCCATCGCCAATGGTTGCATCTTCCTGCAGTCCCGC TCCCCTACGAGGGCCCCGCCCCCCTGGAGGCCCTCGCCAATGGTTGCATCTTCCTGCAGTCCCGC A C MGAT5B Ensembl:ENSG00000167889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76924972..76943980 32194978 MeRIP-seq:(Medium) rs1325469970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1872792,Human_Splice_Rec_1872793,Human_Splice_Rec_1872826,Human_Splice_Rec_1872827,Human_Splice_Rec_1872876,Human_Splice_Rec_1872877,Human_Splice_Rec_1872904,Human_Splice_Rec_1872905 RMVar_hsa_circ_17114,RMVar_hsa_circ_341162,RMVar_hsa_circ_296879,RMVar_hsa_circ_187274,RMVar_hsa_circ_187276,RMVar_hsa_circ_292895 100508 RMVar_ID_100508 Human_SNP_ID_633280402 m1A Human chr17 + 76940453 76940453 76940453 TCCCCTACGAGGGCCCCGCCCCCCTGGAGGCCATCGCCAATGGTTGCATCTTCCTGCAGTCCCGC TCCCCTACGAGGGCCCCGCCCCCCTGGAGGCCGTCGCCAATGGTTGCATCTTCCTGCAGTCCCGC A G MGAT5B Ensembl:ENSG00000167889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:76924972..76943980 32194978 MeRIP-seq:(Medium) rs1325469970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1872792,Human_Splice_Rec_1872793,Human_Splice_Rec_1872826,Human_Splice_Rec_1872827,Human_Splice_Rec_1872876,Human_Splice_Rec_1872877,Human_Splice_Rec_1872904,Human_Splice_Rec_1872905 RMVar_hsa_circ_17114,RMVar_hsa_circ_341162,RMVar_hsa_circ_296879,RMVar_hsa_circ_187274,RMVar_hsa_circ_187276,RMVar_hsa_circ_292895 100509 RMVar_ID_100509 Human_SNP_ID_633319630 m1A Human chr17 + 77088762 77088762 77088762 CGCCTCCTGGTGGTCGCCGACTCGCAGTCCGCAGGATGACTCAGGGCAGCCCTGACCACAGTTCC CGCCTCCTGGTGGTCGCCGACTCGCAGTCCGCGGGATGACTCAGGGCAGCCCTGACCACAGTTCC A G SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77088711..77088859 26863196 MeRIP-seq:(Medium) rs1244293031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1543292,Human_RBP_ID_13176514,Human_RBP_ID_18419745,Human_RBP_ID_18709742,Human_RBP_ID_22959681 100510 RMVar_ID_100510 Human_SNP_ID_633333245 m1A Human chr17 - 77140987 77140987 77140987 CCGCGACCGTAGCTCGACCGCCGGTTCCGGGGAGGGGGCCGGGGAGGCGGGAGGGGGAAGGGGCG CCGCGACCGTAGCTCGACCGCCGGTTCCGGGGGGGGGGCCGGGGAGGCGGGAGGGGGAAGGGGCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:77140937..77141167 26863196 MeRIP-seq:(Medium) rs1056540903 Functional Loss SNV dbSNP153 33..33 33 - - - 100511 RMVar_ID_100511 Human_SNP_ID_633333249 m1A Human chr17 - 77141003 77141003 77141003 TCTCGGTTCCACTGCTCCGCGACCGTAGCTCGACCGCCGGTTCCGGGGAGGGGGCCGGGGAGGCG TCTCGGTTCCACTGCTCCGCGACCGTAGCTCGCCCGCCGGTTCCGGGGAGGGGGCCGGGGAGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77140952..77141148 26863196 MeRIP-seq:(Medium) rs187975190 Functional Loss SNV dbSNP153 33..33 33 - - - 100512 RMVar_ID_100512 Human_SNP_ID_633333262 m1A Human chr17 + 77141028 77141028 77141028 CCGGCGGTCGAGCTACGGTCGCGGAGCAGTGGAACCGAGACTGCCCCGCGGAGCCGCCGGTATGA CCGGCGGTCGAGCTACGGTCGCGGAGCAGTGGGACCGAGACTGCCCCGCGGAGCCGCCGGTATGA A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77140979..77141146 26863196 MeRIP-seq:(Medium) rs1274711242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4453818,Human_RBP_ID_17378553,Human_RBP_ID_18989336 Human_Splice_Rec_1873131,Human_Splice_Rec_1873135,Human_Splice_Rec_1873167,Human_Splice_Rec_1873199,Human_Splice_Rec_1873233 100513 RMVar_ID_100513 Human_SNP_ID_633353636 m1A Human chr17 - 77213982 77213979 77213982 GATCATGGAGCTGGAGTGGGACTGGCTGGAGGAGGTGGTGGCGGCACTCAGCTGGGAGAAGCCGC GATCATGGAGCTGGAGTGGGACTGGCTGGAGG___TGGTGGCGGCACTCAGCTGGGAGAAGCCGC ACCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:77213933..77214083 26863196 MeRIP-seq:(Medium) rs1567940534 Functional Loss DEL dbSNP153 33..35 33 - - - 100514 RMVar_ID_100514 Human_SNP_ID_633353637 m1A Human chr17 - 77213982 77213982 77213982 GATCATGGAGCTGGAGTGGGACTGGCTGGAGGAGGTGGTGGCGGCACTCAGCTGGGAGAAGCCGC GATCATGGAGCTGGAGTGGGACTGGCTGGAGGGGGTGGTGGCGGCACTCAGCTGGGAGAAGCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:77213933..77214083 26863196 MeRIP-seq:(Medium) rs747475365 Functional Loss SNV dbSNP153 33..33 33 - - - 100515 RMVar_ID_100515 Human_SNP_ID_633353844 m1A Human chr17 - 77214552 77214552 77214552 AGGTACTCCGCAGGCAACCTCTGAATCCTCAGAGGATAAGGACCTCAAGGGCTGGCCCTAAGTCC AGGTACTCCGCAGGCAACCTCTGAATCCTCAGGGGATAAGGACCTCAAGGGCTGGCCCTAAGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:77214400..77214801 32194978 MeRIP-seq:(Medium) rs1393757263 Functional Loss SNV dbSNP153 33..33 33 - - - 100516 RMVar_ID_100516 Human_SNP_ID_633354318 m1A Human chr17 + 77215925 77215925 77215925 GTAGGTAGGGCTAGTAGGTAGGGTTAGTAGGTAGGGTTCGTAGGTAGGGTTCGTAGGTAGGGTTA GTAGGTAGGGCTAGTAGGTAGGGTTAGTAGGTGGGGTTCGTAGGTAGGGTTCGTAGGTAGGGTTA A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:77215889..77216002 26863196 MeRIP-seq:(Medium) rs1246987885 Functional Loss SNV dbSNP153 33..33 33 - - - 100517 RMVar_ID_100517 Human_SNP_ID_633354328 m1A Human chr17 - 77215955 77215945 77215955 TACCTACTAACCCTACCTACGAACCCTACCTAACCCTACCTACGAACCCTACCTACGAACCCTAC TACCTACTAACCCTACCTACGAACCCTACCTA__________CGAACCCTACCTACGAACCCTAC GTAGGTAGGGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:77215663..77216000;chr17:77215678..77216000 26863196 MeRIP-seq:(Medium) rs1399211948 Functional Loss DEL dbSNP153 33..42 33 - - - 100518 RMVar_ID_100518 Human_SNP_ID_633354330 m1A Human chr17 - 77215956 77215951 77215956 CTACCTACTAACCCTACCTACGAACCCTACCTAACCCTACCTACGAACCCTACCTACGAACCCTA CTACCTACTAACCCTACCTACGAACCCTACCT_____TACCTACGAACCCTACCTACGAACCCTA AGGGTT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:77215689..77216000;chr17:77215676..77216004 26863196 MeRIP-seq:(Medium) rs1386749208 Functional Loss DEL dbSNP153 33..37 33 - - - 100519 RMVar_ID_100519 Human_SNP_ID_633354330 m1A Human chr17 - 77215955 77215951 77215956 TACCTACTAACCCTACCTACGAACCCTACCTAACCCTACCTACGAACCCTACCTACGAACCCTAC TACCTACTAACCCTACCTACGAACCCTACCT_____TACCTACGAACCCTACCTACGAACCCTAC AGGGTT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:77215663..77216000;chr17:77215678..77216000 26863196 MeRIP-seq:(Medium) rs1386749208 Functional Loss DEL dbSNP153 32..36 33 - - - 100520 RMVar_ID_100520 Human_SNP_ID_633354332 m1A Human chr17 - 77215955 77215955 77215955 TACCTACTAACCCTACCTACGAACCCTACCTAACCCTACCTACGAACCCTACCTACGAACCCTAC TACCTACTAACCCTACCTACGAACCCTACCTACCCCTACCTACGAACCCTACCTACGAACCCTAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:77215663..77216000;chr17:77215678..77216000 26863196 MeRIP-seq:(Medium) rs1176427504 Functional Loss SNV dbSNP153 33..33 33 - - - 100521 RMVar_ID_100521 Human_SNP_ID_633373378 m1A Human chr17 + 77281529 77281529 77281529 CCGCCACACTTTCCTGGGAGCGGCGGCCACGGAGGCACCATGAAGAAGTCTTACTCAGGTGGGCT CCGCCACACTTTCCTGGGAGCGGCGGCCACGGCGGCACCATGAAGAAGTCTTACTCAGGTGGGCT A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77281481..77281646 26863196 MeRIP-seq:(Medium) rs8070026 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9376914,Human_RBP_ID_18419747,Human_RBP_ID_22959682,Human_RBP_ID_26334196 Human_Splice_Rec_1873353,Human_Splice_Rec_1873359,Human_Splice_Rec_1873379 100522 RMVar_ID_100522 Human_SNP_ID_633373379 m1A Human chr17 + 77281529 77281529 77281529 CCGCCACACTTTCCTGGGAGCGGCGGCCACGGAGGCACCATGAAGAAGTCTTACTCAGGTGGGCT CCGCCACACTTTCCTGGGAGCGGCGGCCACGGTGGCACCATGAAGAAGTCTTACTCAGGTGGGCT A T SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77281481..77281646 26863196 MeRIP-seq:(Medium) rs8070026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376914,Human_RBP_ID_18419747,Human_RBP_ID_22959682,Human_RBP_ID_26334196 Human_Splice_Rec_1873353,Human_Splice_Rec_1873359,Human_Splice_Rec_1873379 100523 RMVar_ID_100523 Human_SNP_ID_633373391 m1A Human chr17 - 77281556 77281555 77281556 ACCGACCCCTCCCCACCCCGGGCGCGAAGCCCACCTGAGTAAGACTTCTTCATGGTGCCTCCGTG ACCGACCCCTCCCCACCCCGGGCGCGAAGCCC_CCTGAGTAAGACTTCTTCATGGTGCCTCCGTG GT G SEPTIN9-DT Ensembl:ENSG00000263718 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77281520..77281632 26863196 MeRIP-seq:(Medium) rs749692347 Functional Loss DEL dbSNP153 33..33 33 - - - 100524 RMVar_ID_100524 Human_SNP_ID_633373969 m1A Human chr17 - 77283787 77283787 77283787 GCACATAAAGTGTCTTCGATGACTGTCTATAGACCCACGGTACTTGAGATTGCCCCAACACATCC GCACATAAAGTGTCTTCGATGACTGTCTATAGGCCCACGGTACTTGAGATTGCCCCAACACATCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77283783..77283901 26863196 MeRIP-seq:(Medium) rs913508285 Functional Loss SNV dbSNP153 33..33 33 - - - 100525 RMVar_ID_100525 Human_SNP_ID_633377372 m1A Human chr17 + 77296409 77296409 77296409 ACAGAGAGAGAGAGAGACAGGCAGACACAGACAGACAGGCAGACAAATGGCTAGATAGACAAGCA ACAGAGAGAGAGAGAGACAGGCAGACACAGACCGACAGGCAGACAAATGGCTAGATAGACAAGCA A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77296394..77296508 26863196 MeRIP-seq:(Medium) rs930982361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340134 100526 RMVar_ID_100526 Human_SNP_ID_633377494 m1A Human chr17 + 77296890 77296890 77296890 GAAAAAAAAGATAGATAGATGAATGGATAGATAGCTAGATAGATGACAGATGGATGATAGGTAGA GAAAAAAAAGATAGATAGATGAATGGATAGATGGCTAGATAGATGACAGATGGATGATAGGTAGA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77296883..77297089 26863196 MeRIP-seq:(Medium) rs1412788351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9880786 RMVar_hsa_circ_340134 100527 RMVar_ID_100527 Human_SNP_ID_633379822 m1A Human chr17 + 77306122 77306122 77306122 GTGAATGGATGGATGGATGGGTGAATGGAGTAAATGAGTGGGTGGATGGATGGATGGATGCTGCA GTGAATGGATGGATGGATGGGTGAATGGAGTATATGAGTGGGTGGATGGATGGATGGATGCTGCA A T SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77306110..77306194 26863196 MeRIP-seq:(Medium) rs529718065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189931,Human_RBP_ID_9424190,Human_RBP_ID_17264176,Human_RBP_ID_18942153,Human_RBP_ID_23114320,Human_RBP_ID_24552359 RMVar_hsa_circ_340134 100528 RMVar_ID_100528 Human_SNP_ID_633383522 m1A Human chr17 + 77320347 77320347 77320347 ATATCCGTAGGAATGGAGAGGGACCGGATCTCAGGTACGCAGACAGCCCCCTCCCCATCGGCCGC ATATCCGTAGGAATGGAGAGGGACCGGATCTCGGGTACGCAGACAGCCCCCTCCCCATCGGCCGC A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:77320234..77320384 26863196 MeRIP-seq:(Medium) rs1220095402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3545828 Human_Splice_Rec_1873455,Human_Splice_Rec_1873475,Human_Splice_Rec_1873507 RMVar_hsa_circ_360688 100529 RMVar_ID_100529 Human_SNP_ID_633385775 m1A Human chr17 + 77328868 77328868 77328868 TGAAGAAGCTAAGAACAGGTTGCTGGGGGTGCATATCTGTGTGTGTGGCGAGGGGATTAATGGAA TGAAGAAGCTAAGAACAGGTTGCTGGGGGTGCGTATCTGTGTGTGTGGCGAGGGGATTAATGGAA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77328860..77329043 26863196 MeRIP-seq:(Medium) rs888067441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8092026 RMVar_hsa_circ_360688 100530 RMVar_ID_100530 Human_SNP_ID_633394633 m1A Human chr17 + 77363104 77363104 77363104 CCGGCCTTGCTGAGCTCCACTCTGTATGCACCAGGTGACAGAGGCTGCCCAGGACGGTGGGCAGG CCGGCCTTGCTGAGCTCCACTCTGTATGCACCGGGTGACAGAGGCTGCCCAGGACGGTGGGCAGG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:77363102..77363222 32194978 MeRIP-seq:(Medium) rs115025731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360688 100531 RMVar_ID_100531 Human_SNP_ID_633397330 m1A Human chr17 - 77373453 77373453 77373453 GCAGCGGGTCGCGCGGAGGGCAGCGGCGAGGAAGCGCCCCCGGCGGGGCCCGGGCCCTGCGCGCT GCAGCGGGTCGCGCGGAGGGCAGCGGCGAGGATGCGCCCCCGGCGGGGCCCGGGCCCTGCGCGCT T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:77373351..77373525 26863410 MeRIP-seq:(Medium) rs899518094 Functional Loss SNV dbSNP153 33..33 33 - - - 100532 RMVar_ID_100532 Human_SNP_ID_633397331 m1A Human chr17 - 77373453 77373453 77373453 GCAGCGGGTCGCGCGGAGGGCAGCGGCGAGGAAGCGCCCCCGGCGGGGCCCGGGCCCTGCGCGCT GCAGCGGGTCGCGCGGAGGGCAGCGGCGAGGACGCGCCCCCGGCGGGGCCCGGGCCCTGCGCGCT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:77373351..77373525 26863410 MeRIP-seq:(Medium) rs899518094 Functional Loss SNV dbSNP153 33..33 33 - - - 100533 RMVar_ID_100533 Human_SNP_ID_633405464 m1A Human chr17 + 77402455 77402455 77402455 TCGGAGGACGGAGATCACCATCGTCAAACCCCAGGAGTCAGCCCACCGGAGGATGGAGCCCCCTG TCGGAGGACGGAGATCACCATCGTCAAACCCCGGGAGTCAGCCCACCGGAGGATGGAGCCCCCTG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:77402368..77402625 26863196 MeRIP-seq:(Medium) rs376473706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26332446,Human_RBP_ID_26814033 Human_Splice_Rec_1873499 Human_miRNA_ID_2041254,Human_miRNA_ID_2454551,Human_miRNA_ID_2874061,Human_miRNA_ID_2982023,Human_miRNA_ID_3020237 RMVar_hsa_circ_52125,RMVar_hsa_circ_274220,RMVar_hsa_circ_360688,RMVar_hsa_circ_187289 100534 RMVar_ID_100534 Human_SNP_ID_633405485 m1A Human chr17 - 77402497 77402497 77402497 CGTCGGTGGCAGGGGCAGTGGGCACCTCGGGGACCTTGGAGGCAGGGGGCTCCATCCTCCGGTGG CGTCGGTGGCAGGGGCAGTGGGCACCTCGGGGGCCTTGGAGGCAGGGGGCTCCATCCTCCGGTGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:77402386..77402553 26863196 MeRIP-seq:(Medium) rs752469248 Functional Loss SNV dbSNP153 33..33 33 - - - 100535 RMVar_ID_100535 Human_SNP_ID_633405486 m1A Human chr17 - 77402497 77402497 77402497 CGTCGGTGGCAGGGGCAGTGGGCACCTCGGGGACCTTGGAGGCAGGGGGCTCCATCCTCCGGTGG CGTCGGTGGCAGGGGCAGTGGGCACCTCGGGGCCCTTGGAGGCAGGGGGCTCCATCCTCCGGTGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:77402386..77402553 26863196 MeRIP-seq:(Medium) rs752469248 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 100536 RMVar_ID_100536 Human_SNP_ID_633405500 m1A Human chr17 + 77402523 77402522 77402523 CCAAGGTCCCCGAGGTGCCCACTGCCCCTGCCACCGACGCAGCCCCCAAGAGGGTGGAGATCCAG CCAAGGTCCCCGAGGTGCCCACTGCCCCTGCC_CCGACGCAGCCCCCAAGAGGGTGGAGATCCAG CA C SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77402472..77402565 26863196 MeRIP-seq:(Medium) rs1416817915 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18190969 RMVar_hsa_circ_52125,RMVar_hsa_circ_274220,RMVar_hsa_circ_360688,RMVar_hsa_circ_187289 100537 RMVar_ID_100537 Human_SNP_ID_633405560 m1A Human chr17 - 77402627 77402625 77402627 TTGGGCTCCAGCCTGCTCTGCAGCTGAGACACAGGGGCAGGCTCTGAATTCTCCAAGGTCTGGGC TTGGGCTCCAGCCTGCTCTGCAGCTGAGACAC__GGGCAGGCTCTGAATTCTCCAAGGTCTGGGC CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:77402576..77402675 32194978 MeRIP-seq:(Medium) rs1263575271 Functional Loss DEL dbSNP153 33..34 33 - - - 100538 RMVar_ID_100538 Human_SNP_ID_633405562 m1A Human chr17 - 77402627 77402627 77402627 TTGGGCTCCAGCCTGCTCTGCAGCTGAGACACAGGGGCAGGCTCTGAATTCTCCAAGGTCTGGGC TTGGGCTCCAGCCTGCTCTGCAGCTGAGACACCGGGGCAGGCTCTGAATTCTCCAAGGTCTGGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:77402576..77402675 32194978 MeRIP-seq:(Medium) rs1303472457 Functional Loss SNV dbSNP153 33..33 33 - - - 100539 RMVar_ID_100539 Human_SNP_ID_633407785 m1A Human chr17 + 77410717 77410714 77410718 GCAGGGTGGAGCGCCTGGGGGATTCGTGTTAAACAAGCACATAAACAAAAGCCAACACAACCCTT GCAGGGTGGAGCGCCTGGGGGATTCGTGTT____AAGCACATAAACAAAAGCCAACACAACCCTT TAAAC T SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:77410593..77410839 26863196 MeRIP-seq:(Medium) rs1228397169 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3543553,Human_RBP_ID_8092053,Human_RBP_ID_18487657,Human_RBP_ID_22698586,Human_RBP_ID_22716788 RMVar_hsa_circ_52125 100540 RMVar_ID_100540 Human_SNP_ID_633409328 m1A Human chr17 - 77415793 77415793 77415793 CATCTGCCTTATTTTGCTCCTTATGCCTCCGCACCGTCCACCTCGCCATGCTTCCCTCGTGTGCC CATCTGCCTTATTTTGCTCCTTATGCCTCCGCCCCGTCCACCTCGCCATGCTTCCCTCGTGTGCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77415792..77415884 26863196 MeRIP-seq:(Medium) rs1347618557 Functional Loss SNV dbSNP153 33..33 33 - - - 100541 RMVar_ID_100541 Human_SNP_ID_633416878 m1A Human chr17 + 77444836 77444836 77444836 GGCTCGGGCTAAGAAGTAAGTGGGCGGTGGGAAGCTAGAAGCCGTGGTGTAGACCTACTTTGAGA GGCTCGGGCTAAGAAGTAAGTGGGCGGTGGGACGCTAGAAGCCGTGGTGTAGACCTACTTTGAGA A C AC111170.4,SEPTIN9 Ensembl:ENSG00000279801,Ensembl:ENSG00000184640 Other,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:77444738..77445000 26863196 MeRIP-seq:(Medium) rs1016988746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190174,Human_RBP_ID_18942256,Human_RBP_ID_26782721 RMVar_hsa_circ_52125 100542 RMVar_ID_100542 Human_SNP_ID_633418082 m1A Human chr17 + 77449333 77449333 77449333 TCTCTGTGCTCTGGAGACCCTCATTTGGTGACAGCAAGAGGAACCACTGCAAGAGGGGCGGCCAC TCTCTGTGCTCTGGAGACCCTCATTTGGTGACGGCAAGAGGAACCACTGCAAGAGGGGCGGCCAC A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77449330..77449616 26863196 MeRIP-seq:(Medium) rs890323967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18420215,Human_RBP_ID_18486765,Human_RBP_ID_22716833 RMVar_hsa_circ_52125 100543 RMVar_ID_100543 Human_SNP_ID_633422870 m1A Human chr17 - 77466554 77466554 77466554 GGACCCAGGGCCTGGGGTTGACCTACTGTGGGACTCCAACGGTGACCTCCTGGAAGAAATGCCCG GGACCCAGGGCCTGGGGTTGACCTACTGTGGGTCTCCAACGGTGACCTCCTGGAAGAAATGCCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77466549..77466648 26863196 MeRIP-seq:(Medium) rs1487444034 Functional Loss SNV dbSNP153 33..33 33 - - - 100544 RMVar_ID_100544 Human_SNP_ID_633427924 m1A Human chr17 + 77484137 77484137 77484137 AAGCGAGCTAGGCCCCGGGCAGGGTCCCCAACAGGTTGTGGTTGTTCGAGAATTTGCAGCAGTGG AAGCGAGCTAGGCCCCGGGCAGGGTCCCCAACCGGTTGTGGTTGTTCGAGAATTTGCAGCAGTGG A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77484135..77484461 26863196 MeRIP-seq:(Medium) rs947619673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3543740 100545 RMVar_ID_100545 Human_SNP_ID_633428363 m1A Human chr17 + 77484814 77484814 77484814 TTGTGATGGTGGTGATGTGGGTGGTGGTGGTGATTGTGATGGTGGTGGCGATGGTGGTTGTGATG TTGTGATGGTGGTGATGTGGGTGGTGGTGGTGGTTGTGATGGTGGTGGCGATGGTGGTTGTGATG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77484812..77485096 26863196 MeRIP-seq:(Medium) rs1307211627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3543742,Human_RBP_ID_8192364 100546 RMVar_ID_100546 Human_SNP_ID_633428372 m1A Human chr17 - 77484827 77484827 77484827 CCCACATCACCACCATCACAACCACCATCGCCACCACCATCACAATCACCACCACCACCCACATC CCCACATCACCACCATCACAACCACCATCGCCCCCACCATCACAATCACCACCACCACCCACATC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77484823..77485523 26863196 MeRIP-seq:(Medium) rs1161497398 Functional Loss SNV dbSNP153 33..33 33 - - - 100547 RMVar_ID_100547 Human_SNP_ID_633428700 m1A Human chr17 - 77485186 77485184 77485187 CCATCACAATCATCACCATCACCACCACCACCACAATCACCATCACCCACATTACCATCATCACC CCATCACAATCATCACCATCACCACCACCAC___AATCACCATCACCCACATTACCATCATCACC TGTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77485184..77485566 26863196 MeRIP-seq:(Medium) rs1188070025 Functional Loss DEL dbSNP153 32..34 33 - - - 100548 RMVar_ID_100548 Human_SNP_ID_633429962 m1A Human chr17 - 77488693 77488691 77488693 TGCGTGGGGGATGGGGACGAGTCAGCAGGCACATGAGATGCCCTCCCCAAGCAGGTCGTGCATTC TGCGTGGGGGATGGGGACGAGTCAGCAGGCAC__GAGATGCCCTCCCCAAGCAGGTCGTGCATTC CAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77488691..77488814 26863196 MeRIP-seq:(Medium) rs751273910 Functional Loss DEL dbSNP153 33..34 33 - - - 100549 RMVar_ID_100549 Human_SNP_ID_633431173 m1A Human chr17 - 77492677 77492677 77492677 TTCTCGTTCACCAGCCGGTCCTCCGAGTCCTCATCAAATTCCTTCTGGGGGTACACGTCGATGCC TTCTCGTTCACCAGCCGGTCCTCCGAGTCCTCCTCAAATTCCTTCTGGGGGTACACGTCGATGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:77492583..77492760 26863196 MeRIP-seq:(Medium) rs758827553 Functional Loss SNV dbSNP153 33..33 33 - - - 100550 RMVar_ID_100550 Human_SNP_ID_633431193 m1A Human chr17 - 77492718 77492718 77492718 CCCCTGGGAACAACATCCTAGTGGATCCACTCACCCGGAACTTCTCGTTCACCAGCCGGTCCTCC CCCCTGGGAACAACATCCTAGTGGATCCACTCCCCCGGAACTTCTCGTTCACCAGCCGGTCCTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:77492701..77492725 32194978 MeRIP-seq:(Medium) rs918808795 Functional Loss SNV dbSNP153 33..33 33 - - - 100551 RMVar_ID_100551 Human_SNP_ID_633432902 m1A Human chr17 + 77498513 77498477 77498513 CTGCGCCCACCTCACTGACCCGCCCGCCCCCCACCCCCACAGGACGCACATGCAGAACATCAAGG _________________________________CCCCCACAGGACGCACATGCAGAACATCAAGG CCCGCTGCGCCCACCTCACTGACCCGCCCGCCCCCCA C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:77498501..77498747 32194978 MeRIP-seq:(Medium) rs779524121 Functional Loss DEL dbSNP153 1..33 33 - - - 100552 RMVar_ID_100552 Human_SNP_ID_633432945 m1A Human chr17 + 77498513 77498512 77498513 CTGCGCCCACCTCACTGACCCGCCCGCCCCCCACCCCCACAGGACGCACATGCAGAACATCAAGG CTGCGCCCACCTCACTGACCCGCCCGCCCCCC_CCCCCACAGGACGCACATGCAGAACATCAAGG CA C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:77498501..77498747 32194978 MeRIP-seq:(Medium) rs780255057 Functional Loss DEL dbSNP153 33..33 33 - - - 100553 RMVar_ID_100553 Human_SNP_ID_633432946 m1A Human chr17 + 77498513 77498513 77498513 CTGCGCCCACCTCACTGACCCGCCCGCCCCCCACCCCCACAGGACGCACATGCAGAACATCAAGG CTGCGCCCACCTCACTGACCCGCCCGCCCCCCCCCCCCACAGGACGCACATGCAGAACATCAAGG A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:77498501..77498747 32194978 MeRIP-seq:(Medium) rs773443029 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 100554 RMVar_ID_100554 Human_SNP_ID_633432988 m1A Human chr17 + 77498611 77498611 77498611 GTGTGAAGCGCCTCAACGAGGGCAGCAGCGCCATGGCCAACGGCATGGAGGAGAAGGAGCCAGAA GTGTGAAGCGCCTCAACGAGGGCAGCAGCGCCGTGGCCAACGGCATGGAGGAGAAGGAGCCAGAA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:77498560..77498800 26863196 MeRIP-seq:(Medium) rs763179188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066965,Human_RBP_ID_9376946,Human_RBP_ID_18191354 Human_Splice_Rec_1873378,Human_Splice_Rec_1873400,Human_Splice_Rec_1873426,Human_Splice_Rec_1873448,Human_Splice_Rec_1873474,Human_Splice_Rec_1873494,Human_Splice_Rec_1873530,Human_Splice_Rec_1873554,Human_Splice_Rec_1873586,Human_Splice_Rec_1873612,Human_Splice_Rec_1873662,Human_Splice_Rec_1873706,Human_Splice_Rec_1873732,Human_Splice_Rec_1873788,Human_Splice_Rec_1873812 100555 RMVar_ID_100555 Human_SNP_ID_633433001 m1A Human chr17 + 77498632 77498629 77498632 GCAGCAGCGCCATGGCCAACGGCATGGAGGAGAAGGAGCCAGAAGCCCCGGAGATGTAGACGCCA GCAGCAGCGCCATGGCCAACGGCATGGAGG___AGGAGCCAGAAGCCCCGGAGATGTAGACGCCA GAGA G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:77498581..77498700;chr17:77498582..77498666 26863196 MeRIP-seq:(Medium) rs1266630314 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1091221,Human_RBP_ID_9376946 100556 RMVar_ID_100556 Human_SNP_ID_633433003 m1A Human chr17 + 77498632 77498632 77498632 GCAGCAGCGCCATGGCCAACGGCATGGAGGAGAAGGAGCCAGAAGCCCCGGAGATGTAGACGCCA GCAGCAGCGCCATGGCCAACGGCATGGAGGAGGAGGAGCCAGAAGCCCCGGAGATGTAGACGCCA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:77498581..77498700;chr17:77498582..77498666 26863196 MeRIP-seq:(Medium) rs1200437467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1091221,Human_RBP_ID_9376946 100557 RMVar_ID_100557 Human_SNP_ID_633433014 m1A Human chr17 + 77498651 77498651 77498651 CGGCATGGAGGAGAAGGAGCCAGAAGCCCCGGAGATGTAGACGCCACCCTGCCCACCCCCGGGAT CGGCATGGAGGAGAAGGAGCCAGAAGCCCCGGGGATGTAGACGCCACCCTGCCCACCCCCGGGAT A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:77498601..77498725 26863196 MeRIP-seq:(Medium) rs749992229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27457624 100558 RMVar_ID_100558 Human_SNP_ID_633433307 m1A Human chr17 + 77499250 77499250 77499250 GGTCCCCTGCCACCGACTGCCCAGCCACTCCAAGCCCCCTGGCAGCTGCCCCTCCTGGAGCAGAA GGTCCCCTGCCACCGACTGCCCAGCCACTCCACGCCCCCTGGCAGCTGCCCCTCCTGGAGCAGAA A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77499201..77499275 26863196 MeRIP-seq:(Medium) rs747156110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18190979,Human_RBP_ID_23751466,Human_RBP_ID_26459898,Human_RBP_ID_27260508 Human_miRNA_ID_1270295 100559 RMVar_ID_100559 Human_SNP_ID_633599709 m1A Human chr17 + 78117850 78117850 78117850 AGAGGAAGACAGCGGCGCCCAGGAAGGCGGGGAAGCAGAGCAGCGTGAGGAAGACGGTGCTCATG AGAGGAAGACAGCGGCGCCCAGGAAGGCGGGGGAGCAGAGCAGCGTGAGGAAGACGGTGCTCATG A G NONHSAG022874.2 RNACentral:URS00008B7004 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78117791..78117889 26863196 MeRIP-seq:(Medium) rs1239135963 Functional Loss SNV dbSNP153 33..33 33 - - - 100560 RMVar_ID_100560 Human_SNP_ID_633603345 m1A Human chr17 + 78127455 78127455 78127455 AGGTCACTCCATGCCACCGCCGTCAGGGCGCCAAGGTCCTCATGTTCTCAGAAGACCCACTGCCC AGGTCACTCCATGCCACCGCCGTCAGGGCGCCTAGGTCCTCATGTTCTCAGAAGACCCACTGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78127446..78127548 26863196 MeRIP-seq:(Medium) rs900979688 Functional Loss SNV dbSNP153 33..33 33 - - - 100561 RMVar_ID_100561 Human_SNP_ID_633603515 m1A Human chr17 - 78128136 78128136 78128136 CGGGCGCCACCCAGCCTCTCCCCACCTAGCTCAGGAATGGTGCGCCTGGAAACTCCGCTGGACTT CGGGCGCCACCCAGCCTCTCCCCACCTAGCTCTGGAATGGTGCGCCTGGAAACTCCGCTGGACTT T A TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78127952..78128297 26863196 MeRIP-seq:(Medium) rs373159387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541931,Human_RBP_ID_5319289,Human_RBP_ID_8190252,Human_RBP_ID_9422559,Human_RBP_ID_18487732,Human_RBP_ID_18942291,Human_RBP_ID_24371582 100562 RMVar_ID_100562 Human_SNP_ID_633603516 m1A Human chr17 - 78128136 78128136 78128136 CGGGCGCCACCCAGCCTCTCCCCACCTAGCTCAGGAATGGTGCGCCTGGAAACTCCGCTGGACTT CGGGCGCCACCCAGCCTCTCCCCACCTAGCTCGGGAATGGTGCGCCTGGAAACTCCGCTGGACTT T C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78127952..78128297 26863196 MeRIP-seq:(Medium) rs373159387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541931,Human_RBP_ID_5319289,Human_RBP_ID_8190252,Human_RBP_ID_9422559,Human_RBP_ID_18487732,Human_RBP_ID_18942291,Human_RBP_ID_24371582 100563 RMVar_ID_100563 Human_SNP_ID_633603522 m1A Human chr17 - 78128160 78128160 78128160 GGCTGGGGTGGGGGTTCCTGGAAACGGGCGCCACCCAGCCTCTCCCCACCTAGCTCAGGAATGGT GGCTGGGGTGGGGGTTCCTGGAAACGGGCGCCGCCCAGCCTCTCCCCACCTAGCTCAGGAATGGT T C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78128147..78128303 26863196 MeRIP-seq:(Medium) rs1039233089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767083,Human_RBP_ID_3541931,Human_RBP_ID_5318627,Human_RBP_ID_5365085,Human_RBP_ID_8190252,Human_RBP_ID_9326879,Human_RBP_ID_9422559,Human_RBP_ID_17126765,Human_RBP_ID_18420261,Human_RBP_ID_18486802,Human_RBP_ID_18942291,Human_RBP_ID_22740385,Human_RBP_ID_24371582,Human_RBP_ID_27838584 100564 RMVar_ID_100564 Human_SNP_ID_633603523 m1A Human chr17 - 78128160 78128160 78128160 GGCTGGGGTGGGGGTTCCTGGAAACGGGCGCCACCCAGCCTCTCCCCACCTAGCTCAGGAATGGT GGCTGGGGTGGGGGTTCCTGGAAACGGGCGCCCCCCAGCCTCTCCCCACCTAGCTCAGGAATGGT T G TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78128147..78128303 26863196 MeRIP-seq:(Medium) rs1039233089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767083,Human_RBP_ID_3541931,Human_RBP_ID_5318627,Human_RBP_ID_5365085,Human_RBP_ID_8190252,Human_RBP_ID_9326879,Human_RBP_ID_9422559,Human_RBP_ID_17126765,Human_RBP_ID_18420261,Human_RBP_ID_18486802,Human_RBP_ID_18942291,Human_RBP_ID_22740385,Human_RBP_ID_24371582,Human_RBP_ID_27838584 100565 RMVar_ID_100565 Human_SNP_ID_633603657 m1A Human chr17 + 78128631 78128631 78128631 CGCGGCCGCTCACCTGGGAGGCGCCGGGGAGGAGGGGCCGCGCGCGCAGCCAGGGCTCACCTGTG CGCGGCCGCTCACCTGGGAGGCGCCGGGGAGGCGGGGCCGCGCGCGCAGCCAGGGCTCACCTGTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78128581..78128665 26863196 MeRIP-seq:(Medium) rs1032910175 Functional Loss SNV dbSNP153 33..33 33 - - - 100566 RMVar_ID_100566 Human_SNP_ID_633612732 m1A Human chr17 + 78157424 78157424 78157424 AGTTCGTGCGAGTTGGAATCGAAGCCTCTTAAAATGGCAGATGATTTGGACTTCGAGACAGGAGA AGTTCGTGCGAGTTGGAATCGAAGCCTCTTAACATGGCAGATGATTTGGACTTCGAGACAGGAGA A C EIF5AP2,C17orf99 Ensembl:ENSG00000267679,Ensembl:ENSG00000187997 Pseudogene,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78157352..78157447 26863196 MeRIP-seq:(Medium) rs1403628818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8464451,Human_RBP_ID_17494268,Human_RBP_ID_27457699 100567 RMVar_ID_100567 Human_SNP_ID_633616842 m1A Human chr17 + 78170866 78170866 78170866 GTTCTCCTGCATCTATGGTGAGGGCTACAGCAATGCCCACGAGTCTAAGCAGATGTACTGCGTGT GTTCTCCTGCATCTATGGTGAGGGCTACAGCAGTGCCCACGAGTCTAAGCAGATGTACTGCGTGT A G SYNGR2 Ensembl:ENSG00000108639 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78170797..78170997 26863196 MeRIP-seq:(Medium) rs116304880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764780,Human_RBP_ID_1543405,Human_RBP_ID_1870006,Human_RBP_ID_4454492,Human_RBP_ID_8941856,Human_RBP_ID_18190997,Human_RBP_ID_18709969 Human_Splice_Rec_1874634,Human_Splice_Rec_1874640,Human_Splice_Rec_1874656,Human_Splice_Rec_1874658,Human_Splice_Rec_1874662,Human_Splice_Rec_1874666 RMVar_hsa_circ_93042,RMVar_hsa_circ_117256,RMVar_hsa_circ_187316,RMVar_hsa_circ_187317 100568 RMVar_ID_100568 Human_SNP_ID_633617175 m1A Human chr17 + 78171814 78171814 78171814 TGGACGACTTCATCCAGAATTACGTTGACCCCACTCCGGACCCCAACACTGCCTACGCCTCCTAC TGGACGACTTCATCCAGAATTACGTTGACCCCCCTCCGGACCCCAACACTGCCTACGCCTCCTAC A C SYNGR2 Ensembl:ENSG00000108639 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:78171763..78171937;chr17:78171688..78171838 26863196,32194978 MeRIP-seq:(Medium) rs771516867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501319,Human_RBP_ID_768236,Human_RBP_ID_1870008,Human_RBP_ID_9076660,Human_RBP_ID_13179701,Human_RBP_ID_17262184,Human_RBP_ID_17377774,Human_RBP_ID_17494269,Human_RBP_ID_17654344,Human_RBP_ID_18191000,Human_RBP_ID_18208176,Human_RBP_ID_18709972,Human_RBP_ID_22443198,Human_RBP_ID_26461032,Human_RBP_ID_27260635,Human_RBP_ID_27457704 Human_Splice_Rec_1874638,Human_Splice_Rec_1874644,Human_Splice_Rec_1874650,Human_Splice_Rec_1874654,Human_Splice_Rec_1874664,Human_Splice_Rec_1874670 Human_miRNA_ID_1012335,Human_miRNA_ID_1020516,Human_miRNA_ID_1294347,Human_miRNA_ID_1298327 100569 RMVar_ID_100569 Human_SNP_ID_633617176 m1A Human chr17 + 78171814 78171814 78171814 TGGACGACTTCATCCAGAATTACGTTGACCCCACTCCGGACCCCAACACTGCCTACGCCTCCTAC TGGACGACTTCATCCAGAATTACGTTGACCCCGCTCCGGACCCCAACACTGCCTACGCCTCCTAC A G SYNGR2 Ensembl:ENSG00000108639 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:78171763..78171937;chr17:78171688..78171838 26863196,32194978 MeRIP-seq:(Medium) rs771516867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501319,Human_RBP_ID_768236,Human_RBP_ID_1870008,Human_RBP_ID_9076660,Human_RBP_ID_13179701,Human_RBP_ID_17262184,Human_RBP_ID_17377774,Human_RBP_ID_17494269,Human_RBP_ID_17654344,Human_RBP_ID_18191000,Human_RBP_ID_18208176,Human_RBP_ID_18709972,Human_RBP_ID_22443198,Human_RBP_ID_26461032,Human_RBP_ID_27260635,Human_RBP_ID_27457704 Human_Splice_Rec_1874638,Human_Splice_Rec_1874644,Human_Splice_Rec_1874650,Human_Splice_Rec_1874654,Human_Splice_Rec_1874664,Human_Splice_Rec_1874670 Human_miRNA_ID_1012335,Human_miRNA_ID_1020516,Human_miRNA_ID_1294347,Human_miRNA_ID_1298327 100570 RMVar_ID_100570 Human_SNP_ID_633617291 m1A Human chr17 - 78172036 78172036 78172036 TCCTTAGCTGTGTGTCAGCTGCACAGGATGGAACAGGTGAAAGAGAGGGGCTGGCAGTTCCAGGA TCCTTAGCTGTGTGTCAGCTGCACAGGATGGAGCAGGTGAAAGAGAGGGGCTGGCAGTTCCAGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:78171986..78172087 32194978 MeRIP-seq:(Medium) rs780493351 Functional Loss SNV dbSNP153 33..33 33 - - - 100571 RMVar_ID_100571 Human_SNP_ID_633617382 m1A Human chr17 - 78172333 78172331 78172334 CTCCGCTGCACAGGGCAGGTGTGATGGCCCCCACGAGTCTTTGGCAGAGAACGCAGATAATAGCG CTCCGCTGCACAGGGCAGGTGTGATGGCCCC___GAGTCTTTGGCAGAGAACGCAGATAATAGCG CGTG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:78172284..78172385 32194978 MeRIP-seq:(Medium) rs1381418070 Functional Loss DEL dbSNP153 32..34 33 - - - 100572 RMVar_ID_100572 Human_SNP_ID_633617972 m1A Human chr17 + 78174552 78174550 78174552 AGCTCCAGCCTGGGCGATCGTCCCAGCAGCTGAGAGGGAAGCTTTAAGCAGACCAGTGGGTAGGA AGCTCCAGCCTGGGCGATCGTCCCAGCAGCT__GAGGGAAGCTTTAAGCAGACCAGTGGGTAGGA TGA T NONHSAG022880.2 RNACentral:URS00008B38FF lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:78174501..78174725 32194978 MeRIP-seq:(Medium) rs921416643 Functional Loss DEL dbSNP153 32..33 33 - - - 100573 RMVar_ID_100573 Human_SNP_ID_633618213 m1A Human chr17 - 78175167 78175167 78175167 AGCGCCCTCTGTCTTTCCATGGGAGCGCAGCCATTTGGGGCCATCCTGAACCTGGTGCCGCTGGC AGCGCCCTCTGTCTTTCCATGGGAGCGCAGCCGTTTGGGGCCATCCTGAACCTGGTGCCGCTGGC T C TK1 Ensembl:ENSG00000167900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78175050..78175177 26863196 MeRIP-seq:(Medium) rs781030775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4454601,Human_RBP_ID_5237711,Human_RBP_ID_18992517 Human_Splice_Rec_1874680,Human_Splice_Rec_1874692,Human_Splice_Rec_1874702,Human_Splice_Rec_1874712,Human_Splice_Rec_1874724,Human_Splice_Rec_1874734 Human_miRNA_ID_261507 RMVar_hsa_circ_83775,RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187320,RMVar_hsa_circ_187318 100574 RMVar_ID_100574 Human_SNP_ID_633621438 m1A Human chr17 - 78187001 78187001 78187001 TTGGAGAGTACTCGGGTTCGTGAACTTCCCGGAGGCGCAATGAGCTGCATTAACCTGCCCACTGT TTGGAGAGTACTCGGGTTCGTGAACTTCCCGGGGGCGCAATGAGCTGCATTAACCTGCCCACTGT T C TK1 Ensembl:ENSG00000167900 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78186951..78187075 26863196 MeRIP-seq:(Medium) rs772773188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501372,Human_RBP_ID_1289187,Human_RBP_ID_1543436,Human_RBP_ID_1870016,Human_RBP_ID_4465738,Human_RBP_ID_5318638,Human_RBP_ID_8822803,Human_RBP_ID_9326890,Human_RBP_ID_13180018,Human_RBP_ID_18420620,Human_RBP_ID_23751806,Human_RBP_ID_26812832,Human_RBP_ID_26972662,Human_RBP_ID_27457741 Human_Splice_Rec_1874671,Human_Splice_Rec_1874683,Human_Splice_Rec_1874693,Human_Splice_Rec_1874705,Human_Splice_Rec_1874713 Human_miRNA_ID_2013811,Human_miRNA_ID_2760209 RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 100575 RMVar_ID_100575 Human_SNP_ID_633621439 m1A Human chr17 - 78187001 78187001 78187001 TTGGAGAGTACTCGGGTTCGTGAACTTCCCGGAGGCGCAATGAGCTGCATTAACCTGCCCACTGT TTGGAGAGTACTCGGGTTCGTGAACTTCCCGGCGGCGCAATGAGCTGCATTAACCTGCCCACTGT T G TK1 Ensembl:ENSG00000167900 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78186951..78187075 26863196 MeRIP-seq:(Medium) rs772773188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501372,Human_RBP_ID_1289187,Human_RBP_ID_1543436,Human_RBP_ID_1870016,Human_RBP_ID_4465738,Human_RBP_ID_5318638,Human_RBP_ID_8822803,Human_RBP_ID_9326890,Human_RBP_ID_13180018,Human_RBP_ID_18420620,Human_RBP_ID_23751806,Human_RBP_ID_26812832,Human_RBP_ID_26972662,Human_RBP_ID_27457741 Human_Splice_Rec_1874671,Human_Splice_Rec_1874683,Human_Splice_Rec_1874693,Human_Splice_Rec_1874705,Human_Splice_Rec_1874713 Human_miRNA_ID_2013811,Human_miRNA_ID_2760209 RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 100576 RMVar_ID_100576 Human_SNP_ID_633622786 m1A Human chr17 - 78191062 78191062 78191062 ACCCAATGCGGCCACGGAGAGGTCACACTAGTACCTTCAATTCCTATCTGTGAGTAGGTCCTCAA ACCCAATGCGGCCACGGAGAGGTCACACTAGTGCCTTCAATTCCTATCTGTGAGTAGGTCCTCAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78190949..78191075 26863196 MeRIP-seq:(Medium) rs200546836 Functional Loss SNV dbSNP153 33..33 33 - - - 100577 RMVar_ID_100577 Human_SNP_ID_633625531 m1A Human chr17 + 78200464 78200464 78200464 CAGGTTCCCGGTTGGTATTTCCTTATTTGGAAAGACCATCTTTGTAGGTGTTATTAGCTAAAGTC CAGGTTCCCGGTTGGTATTTCCTTATTTGGAAGGACCATCTTTGTAGGTGTTATTAGCTAAAGTC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78200462..78200672 26863196 MeRIP-seq:(Medium) rs1477993933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 100578 RMVar_ID_100578 Human_SNP_ID_633626107 m1A Human chr17 + 78202436 78202432 78202437 GGGCAACAGAGTGAGACTTCGTCTCAAAAAAAAGAAAAGAAAAATTTCTACCACCTGAGCTTGTG GGGCAACAGAGTGAGACTTCGTCTCAAAA_____AAAAGAAAAATTTCTACCACCTGAGCTTGTG AAAAAG A AFMID Ensembl:ENSG00000183077 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78202434..78202518 26863196 MeRIP-seq:(Medium) rs1479547668 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 100579 RMVar_ID_100579 Human_SNP_ID_633630027 m1A Human chr17 - 78214318 78214318 78214318 GCTGCCAGGCAGGGGGCAACGTCGGGGCACCCATGCCGCCGCCGCCACCTCTGCCAACGGGTCCC GCTGCCAGGCAGGGGGCAACGTCGGGGCACCCGTGCCGCCGCCGCCACCTCTGCCAACGGGTCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:78214251..78214450;chr17:78214251..78214350;chr17:78214251..78214385 26863196 MeRIP-seq:(Medium) rs1482323297 Functional Loss SNV dbSNP153 33..33 33 - - - 100580 RMVar_ID_100580 Human_SNP_ID_633630070 m1A Human chr17 - 78214413 78214413 78214413 GAGGCCGGGCAGTCTCACCCGCTCCGGGGTGCAGGCGCAGCCCTCCAAGAAGGGCCAGTTCTTGA GAGGCCGGGCAGTCTCACCCGCTCCGGGGTGCGGGCGCAGCCCTCCAAGAAGGGCCAGTTCTTGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:78214276..78214452 26863196 MeRIP-seq:(Medium) rs1392270102 Functional Loss SNV dbSNP153 33..33 33 - - - 100581 RMVar_ID_100581 Human_SNP_ID_633632748 m1A Human chr17 - 78224304 78224304 78224304 GGCCTGTCTAATCACACAGCAGTGGCAAAAGGAGTATCTGCCAGACGCTTCCTATCACTCTATTC GGCCTGTCTAATCACACAGCAGTGGCAAAAGGGGTATCTGCCAGACGCTTCCTATCACTCTATTC T C lnc-TK1-2 RNACentral:URS00008B91F8 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78224254..78224351 26863196 MeRIP-seq:(Medium) rs1261874635 Functional Loss SNV dbSNP153 33..33 33 - - - 100582 RMVar_ID_100582 Human_SNP_ID_633633027 m1A Human chr17 - 78225339 78225339 78225339 CTGAAAGAAAGTCTAGGCGGTTGCACTTAGACAAGGGCCTACGGCTTTATTAACAGATGTCGAGG CTGAAAGAAAGTCTAGGCGGTTGCACTTAGACTAGGGCCTACGGCTTTATTAACAGATGTCGAGG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:78225288..78225388 32194978 MeRIP-seq:(Medium) rs1205843024 Functional Loss SNV dbSNP153 33..33 33 - - - 100583 RMVar_ID_100583 Human_SNP_ID_633669098 m1A Human chr17 - 78357386 78357386 78357386 GTGGGGAGGGGGGGCGGAAACCCATGCCTCCCAGCTGAGCACTGGGAATGTCAGCCCAGTAAGTA GTGGGGAGGGGGGGCGGAAACCCATGCCTCCCGGCTGAGCACTGGGAATGTCAGCCCAGTAAGTA T C SOCS3 Ensembl:ENSG00000184557 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78357336..78357404 26863196 MeRIP-seq:(Medium) rs1168343124 Functional Loss SNV dbSNP153 33..33 33 - - - 100584 RMVar_ID_100584 Human_SNP_ID_633669512 m1A Human chr17 + 78358693 78358693 78358693 GGAGGAGGGTTCAGTAGGTGGCGAGGGGAAGGAGGGGGCTCCAGGGGGCGGCATGTAGTGGTGCA GGAGGAGGGTTCAGTAGGTGGCGAGGGGAAGGGGGGGGCTCCAGGGGGCGGCATGTAGTGGTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78358648..78358744 26863196 MeRIP-seq:(Medium) rs765317761 Functional Loss SNV dbSNP153 33..33 33 - - - 100585 RMVar_ID_100585 Human_SNP_ID_633669636 m1A Human chr17 - 78359059 78359059 78359059 TCACCCACAGCAAGTTTCCCGCCGCCGGGATGAGCCGCCCCCTGGACACCAGCCTGCGCCTCAAG TCACCCACAGCAAGTTTCCCGCCGCCGGGATGGGCCGCCCCCTGGACACCAGCCTGCGCCTCAAG T C SOCS3 Ensembl:ENSG00000184557 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78359008..78359170 26863196 MeRIP-seq:(Medium) rs868456388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22222218 100586 RMVar_ID_100586 Human_SNP_ID_633669642 m1A Human chr17 + 78359075 78359075 78359075 GTGTCCAGGGGGCGGCTCATCCCGGCGGCGGGAAACTTGCTGTGGGTGACCATGGCGCACGGAGC GTGTCCAGGGGGCGGCTCATCCCGGCGGCGGGGAACTTGCTGTGGGTGACCATGGCGCACGGAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:78359026..78359193 26863196 MeRIP-seq:(Medium) rs1332884782 Functional Loss SNV dbSNP153 33..33 33 - - - 100587 RMVar_ID_100587 Human_SNP_ID_633710968 m1A Human chr17 - 78478498 78478471 78478498 GTGATGGTGGTGGTGAGGGTGATGGTGGTGATAATGATGGTGATAGTGATGGTGGTGATGATGGC GTGATGGTGGTGGTGAGGGTGATGGTGGTGAT___________________________GATGGC CATCACCACCATCACTATCACCATCATT C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78478449..78478576 26863196 MeRIP-seq:(Medium) rs1026033883 Functional Loss DEL dbSNP153 33..59 33 - - - Human_RBP_ID_23752054 RMVar_hsa_circ_97570,RMVar_hsa_circ_187359 100588 RMVar_ID_100588 Human_SNP_ID_633710982 m1A Human chr17 - 78478498 78478495 78478498 GTGATGGTGGTGGTGAGGGTGATGGTGGTGATAATGATGGTGATAGTGATGGTGGTGATGATGGC GTGATGGTGGTGGTGAGGGTGATGGTGGTGAT___GATGGTGATAGTGATGGTGGTGATGATGGC CATT C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78478449..78478576 26863196 MeRIP-seq:(Medium) rs774672736 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_23752054 RMVar_hsa_circ_97570,RMVar_hsa_circ_187359 100589 RMVar_ID_100589 Human_SNP_ID_633710985 m1A Human chr17 - 78478498 78478498 78478498 GTGATGGTGGTGGTGAGGGTGATGGTGGTGATAATGATGGTGATAGTGATGGTGGTGATGATGGC GTGATGGTGGTGGTGAGGGTGATGGTGGTGATGATGATGGTGATAGTGATGGTGGTGATGATGGC T C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78478449..78478576 26863196 MeRIP-seq:(Medium) rs1250011731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23752054 RMVar_hsa_circ_97570,RMVar_hsa_circ_187359 100590 RMVar_ID_100590 Human_SNP_ID_633711122 m1A Human chr17 + 78478733 78478721 78478733 TTACCATCACCACCACTATTGCCATCATCACCACCATCATCACCATCACCACCATCACTATCATC TTACCATCACCACCACTATTG____________CCATCATCACCATCACCACCATCACTATCATC GCCATCATCACCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78478726..78478812 26863196 MeRIP-seq:(Medium) rs1446447026 Functional Loss DEL dbSNP153 22..33 33 - - - 100591 RMVar_ID_100591 Human_SNP_ID_633711132 m1A Human chr17 + 78478733 78478733 78478733 TTACCATCACCACCACTATTGCCATCATCACCACCATCATCACCATCACCACCATCACTATCATC TTACCATCACCACCACTATTGCCATCATCACCTCCATCATCACCATCACCACCATCACTATCATC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78478726..78478812 26863196 MeRIP-seq:(Medium) rs924900681 Functional Loss SNV dbSNP153 33..33 33 - - - 100592 RMVar_ID_100592 Human_SNP_ID_633713845 m1A Human chr17 + 78484959 78484959 78484959 GTCCACCTCGGGCATGTTCATGTCGTCGATGAAGTAGACGAGCTTCTTAGTGCCTGGCGGCCCGT GTCCACCTCGGGCATGTTCATGTCGTCGATGACGTAGACGAGCTTCTTAGTGCCTGGCGGCCCGT A C DNAH17-AS1 Ensembl:ENSG00000267432 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78484910..78485042 26863196 MeRIP-seq:(Medium) rs200203879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5582672 100593 RMVar_ID_100593 Human_SNP_ID_633713896 m1A Human chr17 - 78485056 78485056 78485056 AACAGGCTCTGGCTCAGGAGGCGCAGGCGGGCAGCTGACCCTCTGCCCTCTCTAGGGGTGCTGGA AACAGGCTCTGGCTCAGGAGGCGCAGGCGGGCCGCTGACCCTCTGCCCTCTCTAGGGGTGCTGGA T G DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:78484913..78485075 26863196 MeRIP-seq:(Medium) rs770609667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97570,RMVar_hsa_circ_187359 100594 RMVar_ID_100594 Human_SNP_ID_633715963 m1A Human chr17 - 78490398 78490398 78490398 GCCTCTGTGGAGGTGGGAAGTCTTCCCAGGTGATTGAAGTTTGGGCTGCCATCCAAAGGGTCAGG GCCTCTGTGGAGGTGGGAAGTCTTCCCAGGTGGTTGAAGTTTGGGCTGCCATCCAAAGGGTCAGG T C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:78490376..78490400 26863196 MeRIP-seq:(Medium) rs1402964337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97570,RMVar_hsa_circ_187359 100595 RMVar_ID_100595 Human_SNP_ID_633715984 m1A Human chr17 + 78490447 78490447 78490447 CCACCTCCACAGAGGCCAAGACCTCCCTTCCCACACCAGCCCTTGTTCCCTGGCACTTTGTGCAA CCACCTCCACAGAGGCCAAGACCTCCCTTCCCGCACCAGCCCTTGTTCCCTGGCACTTTGTGCAA A G DNAH17-AS1 Ensembl:ENSG00000267432 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:78490426..78490450 26863196 MeRIP-seq:(Medium) rs1351423463 Functional Loss SNV dbSNP153 33..33 33 - - - 100596 RMVar_ID_100596 Human_SNP_ID_633716579 m1A Human chr17 - 78491768 78491768 78491768 AGGGTCGGAGGAGGACAGGCAGGGCCTCAGGCATGGAGAGGGCACGTAGGAGGGAGGCCACAGAG AGGGTCGGAGGAGGACAGGCAGGGCCTCAGGCGTGGAGAGGGCACGTAGGAGGGAGGCCACAGAG T C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78491717..78491855 26863196 MeRIP-seq:(Medium) rs1281309823 Functional Loss SNV dbSNP153 33..33 33 - - - 100597 RMVar_ID_100597 Human_SNP_ID_633716773 m1A Human chr17 - 78492248 78492248 78492248 CAGTCGGTGGGCTCTGGGGAGAAGCTTCCCCCAGGAGGTGGCGTCACTGGGTTTGCACTTTATGA CAGTCGGTGGGCTCTGGGGAGAAGCTTCCCCCGGGAGGTGGCGTCACTGGGTTTGCACTTTATGA T C DNAH17 Ensembl:ENSG00000187775 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:78492201..78492405 26863196 MeRIP-seq:(Medium) rs1049615893 Functional Loss SNV dbSNP153 33..33 33 - - - 100598 RMVar_ID_100598 Human_SNP_ID_633717468 m1A Human chr17 + 78494057 78494057 78494057 GGGTGACACACCTGAGATTTGCCGCTGCCCGCATTCCCGACGATGAACACGGAGTGGCGGACCTG GGGTGACACACCTGAGATTTGCCGCTGCCCGCGTTCCCGACGATGAACACGGAGTGGCGGACCTG A G DNAH17-AS1 Ensembl:ENSG00000267432 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78494006..78494179 26863196 MeRIP-seq:(Medium) rs774541246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1875526 100599 RMVar_ID_100599 Human_SNP_ID_633778085 m1A Human chr17 + 78678329 78678329 78678329 GAACTCGCCAGCCAGCACAGTCAAAGGACACCACGATGCCACAGGGGGAGGGGCGGGCGGCGCTC GAACTCGCCAGCCAGCACAGTCAAAGGACACCTCGATGCCACAGGGGGAGGGGCGGGCGGCGCTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78678327..78678418 26863196 MeRIP-seq:(Medium) rs1200406300 Functional Loss SNV dbSNP153 33..33 33 - - - 100600 RMVar_ID_100600 Human_SNP_ID_633793804 m1A Human chr17 - 78740257 78740257 78740257 GGGGAGTGGAGATGGGGGACCTGGTTGGCAGCATATCAGAAGATAGCAGCTCCAGGCCTGGTGCA GGGGAGTGGAGATGGGGGACCTGGTTGGCAGCGTATCAGAAGATAGCAGCTCCAGGCCTGGTGCA T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78740255..78740346 26863196 MeRIP-seq:(Medium) rs1488450581 Functional Loss SNV dbSNP153 33..33 33 - - - 100601 RMVar_ID_100601 Human_SNP_ID_633801362 m1A Human chr17 - 78768582 78768582 78768582 GAAATTGATGGATTTGGTTGCCAGTGTTTGGGAGGGACATAGCATTGAAAGGAGATGAAAGAGAC GAAATTGATGGATTTGGTTGCCAGTGTTTGGGGGGGACATAGCATTGAAAGGAGATGAAAGAGAC T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78768578..78768743 26863196 MeRIP-seq:(Medium) rs550804108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23752222 100602 RMVar_ID_100602 Human_SNP_ID_633801363 m1A Human chr17 - 78768582 78768582 78768582 GAAATTGATGGATTTGGTTGCCAGTGTTTGGGAGGGACATAGCATTGAAAGGAGATGAAAGAGAC GAAATTGATGGATTTGGTTGCCAGTGTTTGGGCGGGACATAGCATTGAAAGGAGATGAAAGAGAC T G CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78768578..78768743 26863196 MeRIP-seq:(Medium) rs550804108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23752222 100603 RMVar_ID_100603 Human_SNP_ID_633808525 m1A Human chr17 + 78794030 78794030 78794030 CCCTGGCTACTACTTGGCCTCCGAACCCAACTAACCACCCTAGCAGAAATCATCTTAAACTCCAC CCCTGGCTACTACTTGGCCTCCGAACCCAACTTACCACCCTAGCAGAAATCATCTTAAACTCCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78793979..78794096 26863196 MeRIP-seq:(Medium) rs1441600457 Functional Loss SNV dbSNP153 33..33 33 - - - 100604 RMVar_ID_100604 Human_SNP_ID_633809646 m1A Human chr17 + 78798206 78798204 78798206 CCCACACACACCCCCTTATACACACGCATCCCACACACACCCTTCTCCAAGTGACTAGGACACAC CCCACACACACCCCCTTATACACACGCATCC__CACACACCCTTCTCCAAGTGACTAGGACACAC CCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78798076..78798434 26863196 MeRIP-seq:(Medium) rs759749577 Functional Loss DEL dbSNP153 32..33 33 - - - 100605 RMVar_ID_100605 Human_SNP_ID_633809648 m1A Human chr17 + 78798206 78798206 78798206 CCCACACACACCCCCTTATACACACGCATCCCACACACACCCTTCTCCAAGTGACTAGGACACAC CCCACACACACCCCCTTATACACACGCATCCCGCACACACCCTTCTCCAAGTGACTAGGACACAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78798076..78798434 26863196 MeRIP-seq:(Medium) rs1475723296 Functional Loss SNV dbSNP153 33..33 33 - - - 100606 RMVar_ID_100606 Human_SNP_ID_633809658 m1A Human chr17 + 78798242 78798240 78798242 ACACCCTTCTCCAAGTGACTAGGACACACACCACAGACGCGCCCACACCACACACACCACCCAAC ACACCCTTCTCCAAGTGACTAGGACACACAC__CAGACGCGCCCACACCACACACACCACCCAAC CCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78798191..78798394 26863196 MeRIP-seq:(Medium) rs374603235 Functional Loss DEL dbSNP153 32..33 33 - - - 100607 RMVar_ID_100607 Human_SNP_ID_633811390 m1A Human chr17 - 78803472 78803472 78803472 TGGCCAGCAGGTGGGATGTGTTACGGACGGCCACCACGCGAGCAGCAGGAAGCGGAGGAGGAAAG TGGCCAGCAGGTGGGATGTGTTACGGACGGCCGCCACGCGAGCAGCAGGAAGCGGAGGAGGAAAG T C USP36 Ensembl:ENSG00000055483 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78803426..78803758 26863196 MeRIP-seq:(Medium) rs773848703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46908,Human_RBP_ID_896968,Human_RBP_ID_18470128,Human_RBP_ID_22959282,Human_RBP_ID_26333885,Human_RBP_ID_27457875,Human_RBP_ID_27813172 Human_Splice_Rec_1876061,Human_Splice_Rec_1876113,Human_Splice_Rec_1876153,Human_Splice_Rec_1876191 Human_miRNA_ID_2513061,Human_miRNA_ID_3055883 RMVar_hsa_circ_348349,RMVar_hsa_circ_44264,RMVar_hsa_circ_307069,RMVar_hsa_circ_33852,RMVar_hsa_circ_187377,RMVar_hsa_circ_313016,RMVar_hsa_circ_115608,RMVar_hsa_circ_266631,RMVar_hsa_circ_53603,RMVar_hsa_circ_187378,RMVar_hsa_circ_187379 100608 RMVar_ID_100608 Human_SNP_ID_633811513 m1A Human chr17 + 78803727 78803727 78803727 TGATGTGCTGTGGGAGGCGCGTCTCTGAGCCCAGCCTCTGCGGCTCTCCCACAAAGGTCTTTTTC TGATGTGCTGTGGGAGGCGCGTCTCTGAGCCCGGCCTCTGCGGCTCTCCCACAAAGGTCTTTTTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:78803679..78803809 32194978 MeRIP-seq:(Medium) rs373221256 Functional Loss SNV dbSNP153 33..33 33 - - - 100609 RMVar_ID_100609 Human_SNP_ID_633811652 m1A Human chr17 - 78803969 78803969 78803969 CTGTTTCCTGGCTGTCCCCACAGGGCTGTGTCACCTGCTCCCCAATCATCCAGCCGCCTGCAACC CTGTTTCCTGGCTGTCCCCACAGGGCTGTGTCGCCTGCTCCCCAATCATCCAGCCGCCTGCAACC T C USP36 Ensembl:ENSG00000055483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78803821..78804000 26863196 MeRIP-seq:(Medium) rs1301684015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46912,Human_RBP_ID_19084190,Human_RBP_ID_22062382,Human_RBP_ID_27260797,Human_RBP_ID_27457877 Human_Splice_Rec_1876060,Human_Splice_Rec_1876112,Human_Splice_Rec_1876152,Human_Splice_Rec_1876190 Human_miRNA_ID_2368110,Human_miRNA_ID_3015896 RMVar_hsa_circ_348349,RMVar_hsa_circ_44264,RMVar_hsa_circ_307069,RMVar_hsa_circ_33852,RMVar_hsa_circ_187377,RMVar_hsa_circ_313016,RMVar_hsa_circ_115608,RMVar_hsa_circ_266631,RMVar_hsa_circ_53603,RMVar_hsa_circ_187378,RMVar_hsa_circ_187379 100610 RMVar_ID_100610 Human_SNP_ID_633812944 m1A Human chr17 - 78807465 78807465 78807465 CCAAACTCTCCCAGACACCCACACACATGCCAACCATCCTAGACGACCCTGGAAAGAAGGTGAAG CCAAACTCTCCCAGACACCCACACACATGCCAGCCATCCTAGACGACCCTGGAAAGAAGGTGAAG T C USP36 Ensembl:ENSG00000055483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78807414..78807585 26863196 MeRIP-seq:(Medium) rs375335141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46923,Human_RBP_ID_23752324,Human_RBP_ID_27457880 Human_miRNA_ID_1061819,Human_miRNA_ID_1957614 RMVar_hsa_circ_348349,RMVar_hsa_circ_8986,RMVar_hsa_circ_44264,RMVar_hsa_circ_33852,RMVar_hsa_circ_115608,RMVar_hsa_circ_266631,RMVar_hsa_circ_53603,RMVar_hsa_circ_187379,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380,RMVar_hsa_circ_4542 100611 RMVar_ID_100611 Human_SNP_ID_633817591 m1A Human chr17 - 78821987 78821987 78821987 GGGTCTCCTTTTCAGGTTGGATCGTCAAACGCAGGCTACTACCTTGGTCCATCAAATTTTTGGAG GGGTCTCCTTTTCAGGTTGGATCGTCAAACGCCGGCTACTACCTTGGTCCATCAAATTTTTGGAG T G USP36 Ensembl:ENSG00000055483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78821894..78822044 26863196 MeRIP-seq:(Medium) rs750077139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1543664,Human_RBP_ID_2524610,Human_RBP_ID_13184190,Human_RBP_ID_18439782,Human_RBP_ID_18989405,Human_RBP_ID_22656910 Human_Splice_Rec_1876042,Human_Splice_Rec_1876043,Human_Splice_Rec_1876094,Human_Splice_Rec_1876095,Human_Splice_Rec_1876134,Human_Splice_Rec_1876135,Human_Splice_Rec_1876172,Human_Splice_Rec_1876173,Human_Splice_Rec_1876200,Human_Splice_Rec_1876201,Human_Splice_Rec_1876230,Human_Splice_Rec_1876231 RMVar_hsa_circ_348349,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380,RMVar_hsa_circ_35259,RMVar_hsa_circ_370974,RMVar_hsa_circ_374324,RMVar_hsa_circ_50997,RMVar_hsa_circ_187384,RMVar_hsa_circ_187385,RMVar_hsa_circ_46408,RMVar_hsa_circ_187386,RMVar_hsa_circ_30113,RMVar_hsa_circ_317622,RMVar_hsa_circ_337306,RMVar_hsa_circ_366140,RMVar_hsa_circ_118645,RMVar_hsa_circ_187387,RMVar_hsa_circ_314563,RMVar_hsa_circ_332789,RMVar_hsa_circ_336429,RMVar_hsa_circ_317289,RMVar_hsa_circ_60096,RMVar_hsa_circ_187390,RMVar_hsa_circ_187391,RMVar_hsa_circ_187394,RMVar_hsa_circ_326646,RMVar_hsa_circ_330784,RMVar_hsa_circ_276267,RMVar_hsa_circ_187393 100612 RMVar_ID_100612 Human_SNP_ID_633817810 m1A Human chr17 + 78822692 78822690 78822692 GGCTGCCTGGCGCCTCCCACGCCTACGTATCCATATGGTAGCTACTCACGCTGGAAGGTTCTGAA GGCTGCCTGGCGCCTCCCACGCCTACGTATC__TATGGTAGCTACTCACGCTGGAAGGTTCTGAA CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78822673..78822756 26863196 MeRIP-seq:(Medium) rs1261810269 Functional Loss DEL dbSNP153 32..33 33 - - - 100613 RMVar_ID_100613 Human_SNP_ID_633817811 m1A Human chr17 + 78822692 78822692 78822692 GGCTGCCTGGCGCCTCCCACGCCTACGTATCCATATGGTAGCTACTCACGCTGGAAGGTTCTGAA GGCTGCCTGGCGCCTCCCACGCCTACGTATCCGTATGGTAGCTACTCACGCTGGAAGGTTCTGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78822673..78822756 26863196 MeRIP-seq:(Medium) rs986327531 Functional Loss SNV dbSNP153 33..33 33 - - - 100614 RMVar_ID_100614 Human_SNP_ID_633817871 m1A Human chr17 - 78822954 78822912 78822954 CCCGCTTTGTGCCAGTGAGGAGTCGGGGAAGCAGCTGGGGAGACGGGGCTGGAGAGCCTGGGGAG CCCGCTTTGTGCCAGTGAGGAGTCGGGGAAGC_________________________________ AGCTTCCCCTCTCCCCAGGCTCTCCAGCCCCGTCTCCCCAGCT A USP36 Ensembl:ENSG00000055483 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78822911..78823111 26863196 MeRIP-seq:(Medium) rs1411471884 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_8190277,Human_RBP_ID_13184217,Human_RBP_ID_21974632 RMVar_hsa_circ_348349,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380,RMVar_hsa_circ_35259,RMVar_hsa_circ_370974,RMVar_hsa_circ_374324,RMVar_hsa_circ_187384,RMVar_hsa_circ_187385,RMVar_hsa_circ_46408,RMVar_hsa_circ_187386,RMVar_hsa_circ_30113,RMVar_hsa_circ_317622,RMVar_hsa_circ_366140,RMVar_hsa_circ_118645,RMVar_hsa_circ_187387,RMVar_hsa_circ_332789,RMVar_hsa_circ_336429,RMVar_hsa_circ_317289,RMVar_hsa_circ_60096,RMVar_hsa_circ_187390,RMVar_hsa_circ_187391,RMVar_hsa_circ_187394,RMVar_hsa_circ_326646,RMVar_hsa_circ_330784,RMVar_hsa_circ_276267,RMVar_hsa_circ_187393 100615 RMVar_ID_100615 Human_SNP_ID_633818528 m1A Human chr17 + 78825467 78825467 78825467 CTACAGACCAGTGAAAGCTCCCTCATGGACCGACATCTGGTGAGCCTTCATCTCTCCCCTGGCAA CTACAGACCAGTGAAAGCTCCCTCATGGACCGCCATCTGGTGAGCCTTCATCTCTCCCCTGGCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78825454..78825669 26863196 MeRIP-seq:(Medium) rs1405019470 Functional Loss SNV dbSNP153 33..33 33 - - - 100616 RMVar_ID_100616 Human_SNP_ID_633822405 m1A Human chr17 + 78838727 78838727 78838727 GCGCTCCTGGACTGTGGCCTGTTCAAACACCGAAGCCGCAGAGCGGGCGTCAGAGCCTGTGGGAG GCGCTCCTGGACTGTGGCCTGTTCAAACACCGGAGCCGCAGAGCGGGCGTCAGAGCCTGTGGGAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78838678..78838820 26863196 MeRIP-seq:(Medium) rs1350295894 Functional Loss SNV dbSNP153 33..33 33 - - - 100617 RMVar_ID_100617 Human_SNP_ID_633822683 m1A Human chr17 - 78839806 78839806 78839806 GTTGGGTAGAGTGTGGATGGTGTGTGCGTCGGAGGGATTGCTAGTGATTACAGGAACACTTGTCT GTTGGGTAGAGTGTGGATGGTGTGTGCGTCGGCGGGATTGCTAGTGATTACAGGAACACTTGTCT T G USP36 Ensembl:ENSG00000055483 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78839801..78840087 26863196 MeRIP-seq:(Medium) rs1410505113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2524637,Human_RBP_ID_23752442 Human_miRNA_ID_2699265 RMVar_hsa_circ_118645,RMVar_hsa_circ_187387,RMVar_hsa_circ_82685,RMVar_hsa_circ_187397,RMVar_hsa_circ_187402,RMVar_hsa_circ_122116,RMVar_hsa_circ_77407,RMVar_hsa_circ_187403 100618 RMVar_ID_100618 Human_SNP_ID_633822689 m1A Human chr17 + 78839814 78839814 78839814 GTTCCTGTAATCACTAGCAATCCCTCCGACGCACACACCATCCACACTCTACCCAACTCAGGAAG GTTCCTGTAATCACTAGCAATCCCTCCGACGCGCACACCATCCACACTCTACCCAACTCAGGAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:78839812..78839922;chr17:78839810..78839935 26863196 MeRIP-seq:(Medium) rs763755761 Functional Loss SNV dbSNP153 33..33 33 - - - 100619 RMVar_ID_100619 Human_SNP_ID_633822836 m1A Human chr17 + 78840236 78840236 78840236 TTGGCGGCCGCCACTCCAGCCCCAGGCCCAGGACCCCCACGCCACCCGCCAGAAGCAGCAGCATC TTGGCGGCCGCCACTCCAGCCCCAGGCCCAGGGCCCCCACGCCACCCGCCAGAAGCAGCAGCATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78840227..78840838 26863196 MeRIP-seq:(Medium) rs368262130 Functional Loss SNV dbSNP153 33..33 33 - - - 100620 RMVar_ID_100620 Human_SNP_ID_633823077 m1A Human chr17 + 78840781 78840781 78840781 CGGGCGCGCCACAAGCCTACGCAGCCCTGGCGACTCCTTCGGCCCGCGGCCCAGCACGCGCACCA CGGGCGCGCCACAAGCCTACGCAGCCCTGGCGTCTCCTTCGGCCCGCGGCCCAGCACGCGCACCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78840588..78840862 26863196 MeRIP-seq:(Medium) rs1328198707 Functional Loss SNV dbSNP153 33..33 33 - - - 100621 RMVar_ID_100621 Human_SNP_ID_633824197 m1A Human chr17 + 78845028 78845028 78845028 TGGAGAATACCTTGGCCTGGGGCATCGGAGGAAACTCTTGCGAGGATGTGCTACCTCCGTTGAAA TGGAGAATACCTTGGCCTGGGGCATCGGAGGAGACTCTTGCGAGGATGTGCTACCTCCGTTGAAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78844981..78845155 26863196 MeRIP-seq:(Medium) rs1308989372 Functional Loss SNV dbSNP153 33..33 33 - - - 100622 RMVar_ID_100622 Human_SNP_ID_633824207 m1A Human chr17 + 78845059 78845059 78845059 AAACTCTTGCGAGGATGTGCTACCTCCGTTGAAAGTGGGAAGATGAGAGACCGGCTGTAAGAGGA AAACTCTTGCGAGGATGTGCTACCTCCGTTGAGAGTGGGAAGATGAGAGACCGGCTGTAAGAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78845008..78845164 26863196 MeRIP-seq:(Medium) rs1298523718 Functional Loss SNV dbSNP153 33..33 33 - - - 100623 RMVar_ID_100623 Human_SNP_ID_633826415 m1A Human chr17 - 78853050 78853050 78853050 AGAGTTGTTGAAAGTTGACAAGCAGACTGCGCATGTCTCTGATGCTTTGTATCATTCTTGAGCAA AGAGTTGTTGAAAGTTGACAAGCAGACTGCGCGTGTCTCTGATGCTTTGTATCATTCTTGAGCAA T C TIMP2 Ensembl:ENSG00000035862 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78853001..78853156 26863196 MeRIP-seq:(Medium) rs1434302269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501579,Human_RBP_ID_5577819,Human_RBP_ID_9076742,Human_RBP_ID_20173010 Human_miRNA_ID_2432033,Human_miRNA_ID_2838769,Human_miRNA_ID_2856661 RMVar_hsa_circ_85266,RMVar_hsa_circ_87361,RMVar_hsa_circ_108052,RMVar_hsa_circ_112767,RMVar_hsa_circ_90083,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187406,RMVar_hsa_circ_187408,RMVar_hsa_circ_187409,RMVar_hsa_circ_187407,RMVar_hsa_circ_187405 100624 RMVar_ID_100624 Human_SNP_ID_633827135 m1A Human chr17 - 78855779 78855779 78855779 CTGGATGGACTGGGTCACAGAGAAGAACATCAACGGGCACCAGGCCAAGTTCTTCGCCTGCATCA CTGGATGGACTGGGTCACAGAGAAGAACATCAGCGGGCACCAGGCCAAGTTCTTCGCCTGCATCA T C TIMP2 Ensembl:ENSG00000035862 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78855336..78855883 26863196 MeRIP-seq:(Medium) rs757916824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764359,Human_RBP_ID_5577823,Human_RBP_ID_22390024,Human_RBP_ID_22443923,Human_RBP_ID_22761683,Human_RBP_ID_26455996 Human_Splice_Rec_1876322,Human_Splice_Rec_1876330,Human_Splice_Rec_1876338,Human_Splice_Rec_1876344,Human_Splice_Rec_1876350 RMVar_hsa_circ_85266,RMVar_hsa_circ_87361,RMVar_hsa_circ_108052,RMVar_hsa_circ_112767,RMVar_hsa_circ_90083,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187406,RMVar_hsa_circ_187408,RMVar_hsa_circ_187409,RMVar_hsa_circ_187407,RMVar_hsa_circ_187405 100625 RMVar_ID_100625 Human_SNP_ID_633827144 m1A Human chr17 + 78855812 78855812 78855812 TGATGTTCTTCTCTGTGACCCAGTCCATCCAGAGGCACTCGTCCGGGGAGGAGATGTAGCACGGG TGATGTTCTTCTCTGTGACCCAGTCCATCCAGGGGCACTCGTCCGGGGAGGAGATGTAGCACGGG A G AC022966.1 Ensembl:ENSG00000267601 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:78854970..78856017 32194978 MeRIP-seq:(Medium) rs769578055 Functional Loss SNV dbSNP153 33..33 33 - - - 100626 RMVar_ID_100626 Human_SNP_ID_633832560 m1A Human chr17 + 78876086 78876086 78876086 CAGAACAGACGGCTTTGCCCTGACGGCCCCCTATTTCCAGTGCCCTCCTAACCATCCTCTCATCC CAGAACAGACGGCTTTGCCCTGACGGCCCCCTGTTTCCAGTGCCCTCCTAACCATCCTCTCATCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78876083..78876389 26863196 MeRIP-seq:(Medium) rs919220529 Functional Loss SNV dbSNP153 33..33 33 - - - 100627 RMVar_ID_100627 Human_SNP_ID_633839371 m1A Human chr17 - 78899758 78899758 78899758 AACGAGGCCTGGGCTGGGGACATGCGGGTAGGATGGGGAAGGGGGTGTGTCCATGTCACGAGGAA AACGAGGCCTGGGCTGGGGACATGCGGGTAGGTTGGGGAAGGGGGTGTGTCCATGTCACGAGGAA T A TIMP2,CEP295NL Ensembl:ENSG00000035862,Ensembl:ENSG00000178404 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78899756..78899854 26863196 MeRIP-seq:(Medium) rs1049412994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5187747 RMVar_hsa_circ_108052,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187405 100628 RMVar_ID_100628 Human_SNP_ID_633844016 m1A Human chr17 - 78916630 78916630 78916630 AGGAAGGTGGTGTTGAGAGGCTCGCAGTTACCAGGGGAGCAGAGCTCCCACCTGCACTGGGGAAG AGGAAGGTGGTGTTGAGAGGCTCGCAGTTACCCGGGGAGCAGAGCTCCCACCTGCACTGGGGAAG T G TIMP2 Ensembl:ENSG00000035862 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78916624..78916875 26863196 MeRIP-seq:(Medium) rs1260151171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108052,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187405 100629 RMVar_ID_100629 Human_SNP_ID_633846514 m1A Human chr17 - 78925158 78925158 78925158 TCGGCCCCGGCTCAGCCCCCGCCCGCGCCCCCAGCCCGCCGCCGCGAGCAGCGCCCGGACCCCCC TCGGCCCCGGCTCAGCCCCCGCCCGCGCCCCCTGCCCGCCGCCGCGAGCAGCGCCCGGACCCCCC T A TIMP2 Ensembl:ENSG00000035862 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:78925078..78925364 26863196 MeRIP-seq:(Medium) rs1387812879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464833,Human_RBP_ID_5467661,Human_RBP_ID_22443925 RMVar_hsa_circ_108052,RMVar_hsa_circ_187404 100630 RMVar_ID_100630 Human_SNP_ID_633846515 m1A Human chr17 - 78925158 78925158 78925158 TCGGCCCCGGCTCAGCCCCCGCCCGCGCCCCCAGCCCGCCGCCGCGAGCAGCGCCCGGACCCCCC TCGGCCCCGGCTCAGCCCCCGCCCGCGCCCCCCGCCCGCCGCCGCGAGCAGCGCCCGGACCCCCC T G TIMP2 Ensembl:ENSG00000035862 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:78925078..78925364 26863196 MeRIP-seq:(Medium) rs1387812879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464833,Human_RBP_ID_5467661,Human_RBP_ID_22443925 RMVar_hsa_circ_108052,RMVar_hsa_circ_187404 100631 RMVar_ID_100631 Human_SNP_ID_633846545 m1A Human chr17 + 78925244 78925244 78925244 TCACCCTCCTCACCTGCCCCGCTCGGCCGCGCAAACTTTCTCTCCTCTTTGTCTCGGGGGCGCGA TCACCCTCCTCACCTGCCCCGCTCGGCCGCGCCAACTTTCTCTCCTCTTTGTCTCGGGGGCGCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:78924928..78925400;chr17:78925076..78925325 26863196 MeRIP-seq:(Medium) rs1197416630 Functional Loss SNV dbSNP153 33..33 33 - - - 100632 RMVar_ID_100632 Human_SNP_ID_633846546 m1A Human chr17 + 78925244 78925244 78925244 TCACCCTCCTCACCTGCCCCGCTCGGCCGCGCAAACTTTCTCTCCTCTTTGTCTCGGGGGCGCGA TCACCCTCCTCACCTGCCCCGCTCGGCCGCGCGAACTTTCTCTCCTCTTTGTCTCGGGGGCGCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:78924928..78925400;chr17:78925076..78925325 26863196 MeRIP-seq:(Medium) rs1197416630 Functional Loss SNV dbSNP153 33..33 33 - - - 100633 RMVar_ID_100633 Human_SNP_ID_633846574 m1A Human chr17 - 78925320 78925320 78925320 AGAACCGCAGCGCCGCTCGCCCGCCGCCCCCCACCCCGCCGCCCCGCCCGGCGAATTGCGCCCCG AGAACCGCAGCGCCGCTCGCCCGCCGCCCCCCCCCCCGCCGCCCCGCCCGGCGAATTGCGCCCCG T G TIMP2 Ensembl:ENSG00000035862 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:78925059..78925375 26863410 MeRIP-seq:(Medium) rs902922185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4455126 RMVar_hsa_circ_108052,RMVar_hsa_circ_187404 100634 RMVar_ID_100634 Human_SNP_ID_633846593 m1A Human chr17 - 78925344 78925344 78925344 CCGTAGAAGGCAGCGCGGCCGCCGAGAACCGCAGCGCCGCTCGCCCGCCGCCCCCCACCCCGCCG CCGTAGAAGGCAGCGCGGCCGCCGAGAACCGCGGCGCCGCTCGCCCGCCGCCCCCCACCCCGCCG T C TIMP2 Ensembl:ENSG00000035862 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:78925076..78925375 26863196 MeRIP-seq:(Medium) rs1446601018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464835 RMVar_hsa_circ_108052,RMVar_hsa_circ_187404 100635 RMVar_ID_100635 Human_SNP_ID_633858970 m1A Human chr17 - 78971488 78971488 78971488 GGCTCCCCTCCTCGGCTTCCTTCCTCTCTGCAATGACCTTCAACAACCGGCCACCAGATGTCGCC GGCTCCCCTCCTCGGCTTCCTTCCTCTCTGCAGTGACCTTCAACAACCGGCCACCAGATGTCGCC T C LGALS3BP Ensembl:ENSG00000108679 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:78971437..78971579 26863196 MeRIP-seq:(Medium) rs1351674749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904458,Human_RBP_ID_1543710,Human_RBP_ID_1870184,Human_RBP_ID_3538650,Human_RBP_ID_4455137,Human_RBP_ID_5115266,Human_RBP_ID_8464859,Human_RBP_ID_17262226,Human_RBP_ID_17377809,Human_RBP_ID_17494326,Human_RBP_ID_17654356,Human_RBP_ID_18710334,Human_RBP_ID_18942319,Human_RBP_ID_27457920 Human_miRNA_ID_685072,Human_miRNA_ID_887617,Human_miRNA_ID_1064269,Human_miRNA_ID_1075576,Human_miRNA_ID_2728274,Human_miRNA_ID_2728275,Human_miRNA_ID_2939036,Human_miRNA_ID_2939037,Human_miRNA_ID_2977756,Human_miRNA_ID_2977757 RMVar_hsa_circ_83114,RMVar_hsa_circ_121324,RMVar_hsa_circ_187414,RMVar_hsa_circ_187415,RMVar_hsa_circ_187416,RMVar_hsa_circ_377127 100636 RMVar_ID_100636 Human_SNP_ID_633858975 m1A Human chr17 + 78971509 78971507 78971510 GTTGAAGGTCATTGCAGAGAGGAAGGAAGCCGAGGAGGGGAGCCTGCAGTGAGGGCGTCCTGGGG GTTGAAGGTCATTGCAGAGAGGAAGGAAGCC___GAGGGGAGCCTGCAGTGAGGGCGTCCTGGGG CGAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:78971411..78971540 26863196 MeRIP-seq:(Medium) rs1393875423 Functional Loss DEL dbSNP153 32..34 33 - - - 100637 RMVar_ID_100637 Human_SNP_ID_633859469 m1A Human chr17 - 78972602 78972602 78972602 TATGGGGCCAGGCAGCTGCAGGGCTACTGCGCAAGCCTCTTTGCCATCCTCCTCCCCCAGGACCC TATGGGGCCAGGCAGCTGCAGGGCTACTGCGCGAGCCTCTTTGCCATCCTCCTCCCCCAGGACCC T C LGALS3BP Ensembl:ENSG00000108679 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:78972551..78972725 32194978 MeRIP-seq:(Medium) rs1313715250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18470135,Human_RBP_ID_22443937,Human_RBP_ID_27457955 Human_miRNA_ID_2467426 RMVar_hsa_circ_83114,RMVar_hsa_circ_121324,RMVar_hsa_circ_187414,RMVar_hsa_circ_187415 100638 RMVar_ID_100638 Human_SNP_ID_633859586 m1A Human chr17 + 78972953 78972953 78972953 GAGGACAAAGCCCCTGGCGGCCCCAGAGCCTGAGGACGAGACGGCTCACCTGAGAAGGTCCCTGA GAGGACAAAGCCCCTGGCGGCCCCAGAGCCTGTGGACGAGACGGCTCACCTGAGAAGGTCCCTGA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:78972951..78973000 32194978 MeRIP-seq:(Medium) rs761307787 Functional Loss SNV dbSNP153 33..33 33 - - - 100639 RMVar_ID_100639 Human_SNP_ID_633859683 m1A Human chr17 + 78973170 78973170 78973170 TCGCAGCCCCGCTGGCTGTCAAAGATCTGGCCAAGGGCCTCCGAGAGCTCCCTGGAGAGGTCCAG TCGCAGCCCCGCTGGCTGTCAAAGATCTGGCCGAGGGCCTCCGAGAGCTCCCTGGAGAGGTCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78972950..78973176 26863196 MeRIP-seq:(Medium) rs1269568943 Functional Loss SNV dbSNP153 33..33 33 - - - 100640 RMVar_ID_100640 Human_SNP_ID_633860524 m1A Human chr17 + 78975978 78975978 78975978 AGGGGACAGCAGGCCCTACCTTGCCCGAAGGCAGCTCTGCCCAGAGCCTGGGTGGCGTTCTCGAA AGGGGACAGCAGGCCCTACCTTGCCCGAAGGCGGCTCTGCCCAGAGCCTGGGTGGCGTTCTCGAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:78975976..78976050 32194978 MeRIP-seq:(Medium) rs750732967 Functional Loss SNV dbSNP153 33..33 33 - - - 100641 RMVar_ID_100641 Human_SNP_ID_633860902 m1A Human chr17 + 78977083 78977083 78977083 CAGAATATCTCCTTGAAGCTCTGAGCAGCCCCAGGGTGCACCAGCCTTCCACACTTCTGCTTTTG CAGAATATCTCCTTGAAGCTCTGAGCAGCCCCTGGGTGCACCAGCCTTCCACACTTCTGCTTTTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:78977080..78977266 26863196 MeRIP-seq:(Medium) rs1308304714 Functional Loss SNV dbSNP153 33..33 33 - - - 100642 RMVar_ID_100642 Human_SNP_ID_633860917 m1A Human chr17 - 78977141 78977141 78977141 TTCTGGGTGTGGCTGCTGGTTGCAGGAACCCAAGGTGAGCTGAGCCCCTGGGAAATACCAAAAGC TTCTGGGTGTGGCTGCTGGTTGCAGGAACCCATGGTGAGCTGAGCCCCTGGGAAATACCAAAAGC T A LGALS3BP Ensembl:ENSG00000108679 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:78977126..78977225 26863196 MeRIP-seq:(Medium) rs199757886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821713,Human_RBP_ID_904473,Human_RBP_ID_4455231,Human_RBP_ID_22443953,Human_RBP_ID_22957876 Human_Splice_Rec_1876378,Human_Splice_Rec_1876379,Human_Splice_Rec_1876386,Human_Splice_Rec_1876387,Human_Splice_Rec_1876396,Human_Splice_Rec_1876397,Human_Splice_Rec_1876402,Human_Splice_Rec_1876403,Human_Splice_Rec_1876408,Human_Splice_Rec_1876409,Human_Splice_Rec_1876422,Human_Splice_Rec_1876423,Human_Splice_Rec_1876432,Human_Splice_Rec_1876433,Human_Splice_Rec_1876448,Human_Splice_Rec_1876449,Human_Splice_Rec_1876457,Human_Splice_Rec_1876464,Human_Splice_Rec_1876465,Human_Splice_Rec_1876470,Human_Splice_Rec_1876471,Human_Splice_Rec_1876486,Human_Splice_Rec_1876487,Human_Splice_Rec_1876494,Human_Splice_Rec_1876502,Human_Splice_Rec_1876503,Human_Splice_Rec_1876508 RMVar_hsa_circ_87557,RMVar_hsa_circ_187417 100643 RMVar_ID_100643 Human_SNP_ID_633860918 m1A Human chr17 - 78977141 78977141 78977141 TTCTGGGTGTGGCTGCTGGTTGCAGGAACCCAAGGTGAGCTGAGCCCCTGGGAAATACCAAAAGC TTCTGGGTGTGGCTGCTGGTTGCAGGAACCCAGGGTGAGCTGAGCCCCTGGGAAATACCAAAAGC T C LGALS3BP Ensembl:ENSG00000108679 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:78977126..78977225 26863196 MeRIP-seq:(Medium) rs199757886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821713,Human_RBP_ID_904473,Human_RBP_ID_4455231,Human_RBP_ID_22443953,Human_RBP_ID_22957876 Human_Splice_Rec_1876378,Human_Splice_Rec_1876379,Human_Splice_Rec_1876386,Human_Splice_Rec_1876387,Human_Splice_Rec_1876396,Human_Splice_Rec_1876397,Human_Splice_Rec_1876402,Human_Splice_Rec_1876403,Human_Splice_Rec_1876408,Human_Splice_Rec_1876409,Human_Splice_Rec_1876422,Human_Splice_Rec_1876423,Human_Splice_Rec_1876432,Human_Splice_Rec_1876433,Human_Splice_Rec_1876448,Human_Splice_Rec_1876449,Human_Splice_Rec_1876457,Human_Splice_Rec_1876464,Human_Splice_Rec_1876465,Human_Splice_Rec_1876470,Human_Splice_Rec_1876471,Human_Splice_Rec_1876486,Human_Splice_Rec_1876487,Human_Splice_Rec_1876494,Human_Splice_Rec_1876502,Human_Splice_Rec_1876503,Human_Splice_Rec_1876508 RMVar_hsa_circ_87557,RMVar_hsa_circ_187417 100644 RMVar_ID_100644 Human_SNP_ID_633865941 m1A Human chr17 + 78995167 78995167 78995167 CATCACCCGTAGTGGTCGTCCACTCCTTGCCCAGGCCGCCCACGTACAGACGCTCGTCCTTCACT CATCACCCGTAGTGGTCGTCCACTCCTTGCCCGGGCCGCCCACGTACAGACGCTCGTCCTTCACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:78995122..78995219;chr17:78995123..78995258 26863196 MeRIP-seq:(Medium) rs1195108072 Functional Loss SNV dbSNP153 33..33 33 - - - 100645 RMVar_ID_100645 Human_SNP_ID_633866458 m1A Human chr17 - 78997046 78997046 78997046 ACCGGACGGGGGTCGTCTACCAGATCGAAGGCAGCAAAGCCGTGCCCTGGGTGATTCTGTCCGAC ACCGGACGGGGGTCGTCTACCAGATCGAAGGCGGCAAAGCCGTGCCCTGGGTGATTCTGTCCGAC T C CANT1 Ensembl:ENSG00000171302 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78996988..78997138 26863196 MeRIP-seq:(Medium) rs1185857495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22760982,Human_RBP_ID_27260883 Human_Splice_Rec_1876513,Human_Splice_Rec_1876519,Human_Splice_Rec_1876525,Human_Splice_Rec_1876531,Human_Splice_Rec_1876541 RMVar_hsa_circ_123235,RMVar_hsa_circ_121995,RMVar_hsa_circ_187419,RMVar_hsa_circ_187420,RMVar_hsa_circ_97600,RMVar_hsa_circ_84191,RMVar_hsa_circ_23252,RMVar_hsa_circ_187421,RMVar_hsa_circ_187422,RMVar_hsa_circ_30769,RMVar_hsa_circ_312641,RMVar_hsa_circ_187425 100646 RMVar_ID_100646 Human_SNP_ID_633866620 m1A Human chr17 - 78997412 78997412 78997412 GCTCCCACCGCCCGGCCCCCGGCAGGCCCCCCACCCACAATGCACACAACTGGAGGCTCGGCCAG GCTCCCACCGCCCGGCCCCCGGCAGGCCCCCCGCCCACAATGCACACAACTGGAGGCTCGGCCAG T C CANT1 Ensembl:ENSG00000171302 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78997364..78997493 26863196 MeRIP-seq:(Medium) rs1049705256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464845,Human_RBP_ID_17378847,Human_RBP_ID_27458024 Human_miRNA_ID_2071357,Human_miRNA_ID_2071358,Human_miRNA_ID_2445913,Human_miRNA_ID_2445914,Human_miRNA_ID_2447302,Human_miRNA_ID_2447303 RMVar_hsa_circ_123235,RMVar_hsa_circ_121995,RMVar_hsa_circ_187419,RMVar_hsa_circ_187420,RMVar_hsa_circ_97600,RMVar_hsa_circ_84191,RMVar_hsa_circ_23252,RMVar_hsa_circ_187421,RMVar_hsa_circ_187422,RMVar_hsa_circ_30769,RMVar_hsa_circ_312641,RMVar_hsa_circ_187425 100647 RMVar_ID_100647 Human_SNP_ID_633866621 m1A Human chr17 - 78997412 78997412 78997412 GCTCCCACCGCCCGGCCCCCGGCAGGCCCCCCACCCACAATGCACACAACTGGAGGCTCGGCCAG GCTCCCACCGCCCGGCCCCCGGCAGGCCCCCCCCCCACAATGCACACAACTGGAGGCTCGGCCAG T G CANT1 Ensembl:ENSG00000171302 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:78997364..78997493 26863196 MeRIP-seq:(Medium) rs1049705256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464845,Human_RBP_ID_17378847,Human_RBP_ID_27458024 Human_miRNA_ID_2071357,Human_miRNA_ID_2071358,Human_miRNA_ID_2445913,Human_miRNA_ID_2445914,Human_miRNA_ID_2447302,Human_miRNA_ID_2447303 RMVar_hsa_circ_123235,RMVar_hsa_circ_121995,RMVar_hsa_circ_187419,RMVar_hsa_circ_187420,RMVar_hsa_circ_97600,RMVar_hsa_circ_84191,RMVar_hsa_circ_23252,RMVar_hsa_circ_187421,RMVar_hsa_circ_187422,RMVar_hsa_circ_30769,RMVar_hsa_circ_312641,RMVar_hsa_circ_187425 100648 RMVar_ID_100648 Human_SNP_ID_633869527 m1A Human chr17 - 79006197 79006197 79006197 GAATGTGGGTGCCTCCAGAAGCTGGAAGAGGCATGAGAATGGAGCCATGGCCCGTGTGAGGCTTC GAATGTGGGTGCCTCCAGAAGCTGGAAGAGGCCTGAGAATGGAGCCATGGCCCGTGTGAGGCTTC T G CANT1 Ensembl:ENSG00000171302 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79006159..79006347 26863196 MeRIP-seq:(Medium) rs149959549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541962,Human_RBP_ID_9423641,Human_RBP_ID_13184978,Human_RBP_ID_21928160 RMVar_hsa_circ_97600,RMVar_hsa_circ_187421 100649 RMVar_ID_100649 Human_SNP_ID_633869528 m1A Human chr17 - 79006197 79006197 79006199 GAATGTGGGTGCCTCCAGAAGCTGGAAGAGGCATGAGAATGGAGCCATGGCCCGTGTGAGGCTTC GAATGTGGGTGCCTCCAGAAGCTGGAAGAGTCCTGAGAATGGAGCCATGGCCCGTGTGAGGCTTC TGC GGA CANT1 Ensembl:ENSG00000171302 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79006159..79006347 26863196 MeRIP-seq:(Medium) rs386799591 Functional Loss MNV dbSNP153 31..33 33 - - - Human_RBP_ID_3541962,Human_RBP_ID_9423641,Human_RBP_ID_13184978,Human_RBP_ID_21928160 RMVar_hsa_circ_97600,RMVar_hsa_circ_187421 100650 RMVar_ID_100650 Human_SNP_ID_633870477 m1A Human chr17 - 79009709 79009709 79009709 GGCCGTTAGCCCAGCCAAGCCCAGCCAAGCCCAGCCAAGCCCCGCCGATCGCGGGCACCGGAGCC GGCCGTTAGCCCAGCCAAGCCCAGCCAAGCCCTGCCAAGCCCCGCCGATCGCGGGCACCGGAGCC T A CANT1 Ensembl:ENSG00000171302 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr17:79009563..79009775;chr17:79009686..79009769 26863410 MeRIP-seq:(Medium) rs914441096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764085,Human_RBP_ID_4455385 Human_Splice_Rec_1876509,Human_Splice_Rec_1876523,Human_Splice_Rec_1876529,Human_Splice_Rec_1876535,Human_Splice_Rec_1876547,Human_Splice_Rec_1876557,Human_Splice_Rec_1876561,Human_Splice_Rec_1876567,Human_Splice_Rec_1876575,Human_Splice_Rec_1876581,Human_Splice_Rec_1876585,Human_Splice_Rec_1876591,Human_Splice_Rec_1876597 Human_miRNA_ID_2147243,Human_miRNA_ID_2555028,Human_miRNA_ID_2988670,Human_miRNA_ID_3022370,Human_miRNA_ID_3066288 RMVar_hsa_circ_97600,RMVar_hsa_circ_187421 100651 RMVar_ID_100651 Human_SNP_ID_633875003 m1A Human chr17 - 79027504 79027504 79027504 TCCAGGCCAAGGACCCCAGCATAGACCCCAGGACAGGGCCCCAAGGATCCCTGGCTCATGAGAGC TCCAGGCCAAGGACCCCAGCATAGACCCCAGGTCAGGGCCCCAAGGATCCCTGGCTCATGAGAGC T A C1QTNF1-AS1 Ensembl:ENSG00000265096 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79027476..79027649 26863196 MeRIP-seq:(Medium) rs925995104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419764,Human_RBP_ID_22716890 100652 RMVar_ID_100652 Human_SNP_ID_633887989 m1A Human chr17 + 79074983 79074983 79074983 GCCGCGGCGGTGACGGTCACCCGGTCGGCTACACGGCGGCGGCGGCGGCAGCTGCAGGGGCTGGC GCCGCGGCGGTGACGGTCACCCGGTCGGCTACGCGGCGGCGGCGGCGGCAGCTGCAGGGGCTGGC A G ENGASE Ensembl:ENSG00000167280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:79074912..79077477;chr17:79074851..79077500;chr17:79074958..79075087 26863196 MeRIP-seq:(Medium) rs1309091735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768635 100653 RMVar_ID_100653 Human_SNP_ID_633890036 m1A Human chr17 + 79081878 79081878 79081878 GGCCCCATCCTTCTGGGCCTGGGCCTCACAGCAGGTCCTTGTTGCTTCTCAGGGTCTTCTTTGAT GGCCCCATCCTTCTGGGCCTGGGCCTCACAGCGGGTCCTTGTTGCTTCTCAGGGTCTTCTTTGAT A G ENGASE Ensembl:ENSG00000167280 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79081876..79081925 26863196 MeRIP-seq:(Medium) rs1230301388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346304,RMVar_hsa_circ_373275,RMVar_hsa_circ_344659,RMVar_hsa_circ_54050,RMVar_hsa_circ_187430,RMVar_hsa_circ_90891,RMVar_hsa_circ_187433,RMVar_hsa_circ_122186,RMVar_hsa_circ_187434 100654 RMVar_ID_100654 Human_SNP_ID_633890103 m1A Human chr17 - 79082005 79082005 79082005 CCACGTTCCCTCGAGCAAACACATCCACGCCCACGTACACATCAGCCCGGCGCTCCCCAGCCTGC CCACGTTCCCTCGAGCAAACACATCCACGCCCGCGTACACATCAGCCCGGCGCTCCCCAGCCTGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79081956..79082041 26863196 MeRIP-seq:(Medium) rs759194033 Functional Loss SNV dbSNP153 33..33 33 - - - 100655 RMVar_ID_100655 Human_SNP_ID_633890833 m1A Human chr17 - 79083884 79083884 79083884 ACCCCGGACGAGCAGGGAGCTGCCTCCGTGCCAGGCATCCTCCAGGCAGCAGTGCGTCCTCACCC ACCCCGGACGAGCAGGGAGCTGCCTCCGTGCCGGGCATCCTCCAGGCAGCAGTGCGTCCTCACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79083798..79084007 26863196 MeRIP-seq:(Medium) rs1286231782 Functional Loss SNV dbSNP153 33..33 33 - - - 100656 RMVar_ID_100656 Human_SNP_ID_633893429 m1A Human chr17 - 79091106 79091106 79091106 CACCCTGCCCTGCTCAGCTCTGTCTCCTCCTCAGGGCCCCAGGTGTCTCCTCCCATCCTGGGCTG CACCCTGCCCTGCTCAGCTCTGTCTCCTCCTCGGGGCCCCAGGTGTCTCCTCCCATCCTGGGCTG T C RBFOX3 Ensembl:ENSG00000167281 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79091070..79091176 26863196 MeRIP-seq:(Medium) rs951998260 Functional Loss SNV dbSNP153 33..33 33 - - - 100657 RMVar_ID_100657 Human_SNP_ID_634056368 m1A Human chr17 - 79699469 79699364 79699469 TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGAGGTG TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCGGGTCTGAGGTAAGAGTAGGCGGGTCCAGGGTG CGCCCGCTCTCACCTCAGACCTGCCTGCTCTCACCTCAGACCTGCCCACTCTCACCTCAGACCTGCCCACTCTCACCTCAGACCTGCCCACTCTCACCTCAGACCT TGCCCACTCTCACCTCAGACCTGCCTGCTCTCAATCTGGACCCGCCCACTCTCAACCTGGACCCACCCACTGTCACCCTGGACCCGCCTACTCTTACCTCAGACCC - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79699420..79699905 26863196 MeRIP-seq:(Medium) rs1568476966 Functional Loss MNV dbSNP153 33..65 33 - - - 100658 RMVar_ID_100658 Human_SNP_ID_634056399 m1A Human chr17 - 79699469 79699397 79699469 TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGAGGTG TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCGGGTCTGAGGTAAGAGTAGGCGGGTCCAGGGTG CCTCAGACCTGCCCACTCTCACCTCAGACCTGCCCACTCTCACCTCAGACCTGCCCACTCTCACCTCAGACCT ATCTGGACCCGCCCACTCTCAACCTGGACCCACCCACTGTCACCCTGGACCCGCCTACTCTTACCTCAGACCC - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79699420..79699905 26863196 MeRIP-seq:(Medium) rs1568476996 Functional Loss MNV dbSNP153 33..65 33 - - - 100659 RMVar_ID_100659 Human_SNP_ID_634056430 m1A Human chr17 - 79699469 79699435 79699469 TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGAGGTG TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCGGGTCTGAGGTAAGAGTAGGCGGGTCCAGGGTG CTCACCTCAGACCTGCCCACTCTCACCTCAGACCT GTCACCCTGGACCCGCCTACTCTTACCTCAGACCC - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79699420..79699905 26863196 MeRIP-seq:(Medium) rs1568477047 Functional Loss MNV dbSNP153 33..65 33 - - - 100660 RMVar_ID_100660 Human_SNP_ID_634056438 m1A Human chr17 - 79699473 79699452 79699473 AGGTTGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGA AGGTTGAGAGTGGGCGGGTCCAGATTGAGAGC_____________________GGGCAGGTCTGA CACTCTCACCTCAGACCTGCCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79699425..79699701 26863196 MeRIP-seq:(Medium) rs1568477054 Functional Loss DEL dbSNP153 33..53 33 - - - 100661 RMVar_ID_100661 Human_SNP_ID_634056443 m1A Human chr17 - 79699469 79699469 79699469 TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGAGGTG TGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCGGGTCTGAGGTGAGAGTGGGCAGGTCTGAGGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79699420..79699905 26863196 MeRIP-seq:(Medium) rs373827394 Functional Loss SNV dbSNP153 33..33 33 - - - 100662 RMVar_ID_100662 Human_SNP_ID_634056446 m1A Human chr17 - 79699473 79699473 79699473 AGGTTGAGAGTGGGCGGGTCCAGATTGAGAGCAGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGA AGGTTGAGAGTGGGCGGGTCCAGATTGAGAGCGGGCAGGTCTGAGGTGAGAGTGGGCAGGTCTGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79699425..79699701 26863196 MeRIP-seq:(Medium) rs78013666 Functional Loss SNV dbSNP153 33..33 33 - - - 100663 RMVar_ID_100663 Human_SNP_ID_634068586 m1A Human chr17 - 79741746 79741746 79741746 GCACGCGTTGGTCTGGGAGGAGAGGATGGGGCAGGCTGAGGGCAGGTCTGGTGGGACAGGTGAAG GCACGCGTTGGTCTGGGAGGAGAGGATGGGGCGGGCTGAGGGCAGGTCTGGTGGGACAGGTGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79741708..79741866 26863196 MeRIP-seq:(Medium) rs1555824668 Functional Loss SNV dbSNP153 33..33 33 - - - 100664 RMVar_ID_100664 Human_SNP_ID_634078144 m1A Human chr17 - 79778183 79778183 79778183 ACCGCGGCGCCCGCCGCCAGTCACCCGCCCGGACCGCCGCGCGCCCCGCCGGCAGCACACAAAGC ACCGCGGCGCCCGCCGCCAGTCACCCGCCCGGCCCGCCGCGCGCCCCGCCGGCAGCACACAAAGC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:79778163..79778301 26863196 MeRIP-seq:(Medium) rs1555829301 Functional Loss SNV dbSNP153 33..33 33 - - - 100665 RMVar_ID_100665 Human_SNP_ID_634078177 m1A Human chr17 - 79778215 79778215 79778215 CAGCTCCTCCATGCTGCCCGGCAGCCAGCCCGACCGCGGCGCCCGCCGCCAGTCACCCGCCCGGA CAGCTCCTCCATGCTGCCCGGCAGCCAGCCCGGCCGCGGCGCCCGCCGCCAGTCACCCGCCCGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:79778151..79779391;chr17:79778151..79778450;chr17:79778165..79779441 26863196 MeRIP-seq:(Medium) rs782717009 Functional Loss SNV dbSNP153 33..33 33 - - - 100666 RMVar_ID_100666 Human_SNP_ID_634078198 m1A Human chr17 + 79778251 79778251 79778251 GCTGGCTGCCGGGCAGCATGGAGGAGCTGAGCAGCGTGGGCGAGCAGGTCTTCGCCGCCGAGTGC GCTGGCTGCCGGGCAGCATGGAGGAGCTGAGCGGCGTGGGCGAGCAGGTCTTCGCCGCCGAGTGC A G CBX2 Ensembl:ENSG00000173894 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:79778249..79778381 26863196 MeRIP-seq:(Medium) rs1555829349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4455647,Human_RBP_ID_18420272,Human_RBP_ID_18470297,Human_RBP_ID_21890328,Human_RBP_ID_22500626 Human_Splice_Rec_1876953,Human_Splice_Rec_1876961,Human_Splice_Rec_1876965 100667 RMVar_ID_100667 Human_SNP_ID_634078216 m1A Human chr17 - 79778288 79778288 79778288 GGGCCGCACGCACCTTGCGGAGCCGCTTGCTCAGGATGCACTCGGCGGCGAAGACCTGCTCGCCC GGGCCGCACGCACCTTGCGGAGCCGCTTGCTCCGGATGCACTCGGCGGCGAAGACCTGCTCGCCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:79778187..79778384 26863410 MeRIP-seq:(Medium) rs1371871863 Functional Loss SNV dbSNP153 33..33 33 - - - 100668 RMVar_ID_100668 Human_SNP_ID_634081576 m1A Human chr17 + 79786588 79786588 79786588 AGCAGCGTGGGCAGCAAGGCAGGGCAGCCCAGAGGTGGCAGCGGCAGGCAATCTGGTCACTAGGT AGCAGCGTGGGCAGCAAGGCAGGGCAGCCCAGGGGTGGCAGCGGCAGGCAATCTGGTCACTAGGT A G CBX2 Ensembl:ENSG00000173894 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79786539..79786696 26863196 MeRIP-seq:(Medium) rs1336072528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767438,Human_RBP_ID_4455777,Human_RBP_ID_22063384 Human_miRNA_ID_935724,Human_miRNA_ID_955695 100669 RMVar_ID_100669 Human_SNP_ID_634084757 m1A Human chr17 - 79796478 79796478 79796478 GGATGGTCGCAGAAGTAAGTAGGTTATATGCAATTCTCAACCCCAGACTGTTATTCGGGAGGTTT GGATGGTCGCAGAAGTAAGTAGGTTATATGCATTTCTCAACCCCAGACTGTTATTCGGGAGGTTT T A CBX8 Ensembl:ENSG00000141570 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:79796476..79796594 26863196 MeRIP-seq:(Medium) rs186441340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362164,Human_RBP_ID_19084229 Human_Splice_Rec_1876972,Human_Splice_Rec_1876980,Human_Splice_Rec_1876988 100670 RMVar_ID_100670 Human_SNP_ID_634084758 m1A Human chr17 - 79796478 79796478 79796478 GGATGGTCGCAGAAGTAAGTAGGTTATATGCAATTCTCAACCCCAGACTGTTATTCGGGAGGTTT GGATGGTCGCAGAAGTAAGTAGGTTATATGCAGTTCTCAACCCCAGACTGTTATTCGGGAGGTTT T C CBX8 Ensembl:ENSG00000141570 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:79796476..79796594 26863196 MeRIP-seq:(Medium) rs186441340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362164,Human_RBP_ID_19084229 Human_Splice_Rec_1876972,Human_Splice_Rec_1876980,Human_Splice_Rec_1876988 100671 RMVar_ID_100671 Human_SNP_ID_634084961 m1A Human chr17 - 79797000 79797000 79797000 TGGAAGCGGCCAAGGGGGGAAGCGGCGAGTCAACATGGAGCTTTCAGCGGTGGGGGAGCGGGTGT TGGAAGCGGCCAAGGGGGGAAGCGGCGAGTCAGCATGGAGCTTTCAGCGGTGGGGGAGCGGGTGT T C CBX8 Ensembl:ENSG00000141570 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79796866..79797091 26863196 MeRIP-seq:(Medium) rs1405651743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4455862,Human_RBP_ID_22061727 Human_Splice_Rec_1876971 100672 RMVar_ID_100672 Human_SNP_ID_634095965 m1A Human chr17 - 79834555 79834555 79834555 AGGAGGCCTTTGGAGAGCAGCCCCTGCAGCTCACCACCAAGCCCGACCTGCTTGCCTGGGACCCG AGGAGGCCTTTGGAGAGCAGCCCCTGCAGCTCGCCACCAAGCCCGACCTGCTTGCCTGGGACCCG T C CBX4 Ensembl:ENSG00000141582 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:79833949..79834744 26863410 MeRIP-seq:(Medium) rs780734474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22061732 RMVar_hsa_circ_78987,RMVar_hsa_circ_187441 100673 RMVar_ID_100673 Human_SNP_ID_634096125 m1A Human chr17 - 79834870 79834864 79834870 GGGGCAAGATGAAGATAGTCAAGAACAAGAACAAGAACGGACGCATCGTGATCGTGATGAGCAAA GGGGCAAGATGAAGATAGTCAAGAACAAGAAC______GGACGCATCGTGATCGTGATGAGCAAA CGTTCTT C CBX4 Ensembl:ENSG00000141582 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79833720..79835392 26863196 MeRIP-seq:(Medium) rs1388431022 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_1543865,Human_RBP_ID_1870281,Human_RBP_ID_3538746,Human_RBP_ID_8253780,Human_RBP_ID_13185882,Human_RBP_ID_18530961 RMVar_hsa_circ_78987,RMVar_hsa_circ_187441 100674 RMVar_ID_100674 Human_SNP_ID_634097782 m1A Human chr17 - 79839421 79839398 79839421 GCGGCCCGGGCTCAGTTGTCTGAGCGAGCGCGAGCCGGGAGCCGGGGCGGGCGCGGGCAGCGGCG GCGGCCCGGGCTCAGTTGTCTGAGCGAGCGCG_______________________GGCAGCGGCG CCGCGCCCGCCCCGGCTCCCGGCT C CBX4 Ensembl:ENSG00000141582 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:79839329..79839429 26863410 MeRIP-seq:(Medium) rs1205814191 Functional Loss DEL dbSNP153 33..55 33 - - - Human_RBP_ID_4466898 100675 RMVar_ID_100675 Human_SNP_ID_634112786 m1A Human chr17 + 79893712 79893688 79893712 TCACCACCTTCATCATCATCATCATCACCATCATCATCATCATCATCACCATCATCACCATCACC TCACCACCT________________________TCATCATCATCATCACCATCATCACCATCACC TTCATCATCATCATCATCACCATCA T HSALNG0119145 RNACentral:URS0000EAA741 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79893683..79893760 26863196 MeRIP-seq:(Medium) rs1435769816 Functional Loss DEL dbSNP153 10..33 33 - - - 100676 RMVar_ID_100676 Human_SNP_ID_634125089 m1A Human chr17 - 79935929 79935929 79935929 GTCGCATTTCCGGGTAGGAAGGTAGCATTTCAAGTTCAAAGAGAGGTCAAGTCATGCAACCATCT GTCGCATTTCCGGGTAGGAAGGTAGCATTTCAGGTTCAAAGAGAGGTCAAGTCATGCAACCATCT T C TBC1D16 Ensembl:ENSG00000167291 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:79935878..79936028 32194978 MeRIP-seq:(Medium) rs534111451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18296865,Human_RBP_ID_23752855 100677 RMVar_ID_100677 Human_SNP_ID_634125143 m1A Human chr17 - 79936174 79936174 79936174 GCCCACTCCTGCCACGAGACCCATCCTCTGCGATCCCGCCAGGCATGTGTGTGTGAATGCATGTG GCCCACTCCTGCCACGAGACCCATCCTCTGCGGTCCCGCCAGGCATGTGTGTGTGAATGCATGTG T C TBC1D16 Ensembl:ENSG00000167291 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:79936127..79936277 32194978 MeRIP-seq:(Medium) rs1209941687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501883 100678 RMVar_ID_100678 Human_SNP_ID_634125658 m1A Human chr17 + 79937406 79937406 79937406 CAGCATCTTCATCTTGTCCTGATGCCCTGCCCACCCCCGCCGAGCTTCACACTGGGCTGCTATGG CAGCATCTTCATCTTGTCCTGATGCCCTGCCCCCCCCCGCCGAGCTTCACACTGGGCTGCTATGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79937363..79937481 26863196 MeRIP-seq:(Medium) rs1021297187 Functional Loss SNV dbSNP153 33..33 33 - - - 100679 RMVar_ID_100679 Human_SNP_ID_634129684 m1A Human chr17 + 79949860 79949860 79949860 CCGCGGATTGACACATCAATACCGCCAAAGAAAATGGCCTGGAGGAAGCGGCAAAAGTTGGGGAG CCGCGGATTGACACATCAATACCGCCAAAGAAGATGGCCTGGAGGAAGCGGCAAAAGTTGGGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:79949811..79950556 32194978 MeRIP-seq:(Medium) rs939046037 Functional Loss SNV dbSNP153 33..33 33 - - - 100680 RMVar_ID_100680 Human_SNP_ID_634130261 m1A Human chr17 - 79951584 79951584 79951584 CCTTCCAATGGCCCTTCAGCGACGAGGCCTGCACCAGCGGCCAGCTGGTCGTTGCCAGCCGAGAG CCTTCCAATGGCCCTTCAGCGACGAGGCCTGCCCCAGCGGCCAGCTGGTCGTTGCCAGCCGAGAG T G TBC1D16 Ensembl:ENSG00000167291 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:79951458..79952046 32194978 MeRIP-seq:(Medium) rs1245648169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19080285 Human_Splice_Rec_1877064,Human_Splice_Rec_1877132,Human_Splice_Rec_1877162 RMVar_hsa_circ_20497,RMVar_hsa_circ_287981,RMVar_hsa_circ_67068,RMVar_hsa_circ_114082,RMVar_hsa_circ_187444,RMVar_hsa_circ_75869,RMVar_hsa_circ_98559,RMVar_hsa_circ_67776,RMVar_hsa_circ_187447,RMVar_hsa_circ_187448 100681 RMVar_ID_100681 Human_SNP_ID_634145801 m1A Human chr17 - 80010582 80010582 80010582 CCCCGCCCTCGGGGCCGGCGCACCCGGAGCTCAGGAGCCTCCCACCAGCCCTCCCCGACGGAGCT CCCCGCCCTCGGGGCCGGCGCACCCGGAGCTCGGGAGCCTCCCACCAGCCCTCCCCGACGGAGCT T C TBC1D16 Ensembl:ENSG00000167291 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:80010159..80010700;chr17:80010384..80010692 26863196 MeRIP-seq:(Medium) rs1294266412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20497,RMVar_hsa_circ_75869,RMVar_hsa_circ_98559,RMVar_hsa_circ_187447,RMVar_hsa_circ_187448,RMVar_hsa_circ_342317 100682 RMVar_ID_100682 Human_SNP_ID_634145810 m1A Human chr17 - 80010593 80010593 80010593 TTCGCAAGGCACCCCGCCCTCGGGGCCGGCGCACCCGGAGCTCAGGAGCCTCCCACCAGCCCTCC TTCGCAAGGCACCCCGCCCTCGGGGCCGGCGCGCCCGGAGCTCAGGAGCCTCCCACCAGCCCTCC T C TBC1D16 Ensembl:ENSG00000167291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80010543..80010673 26863196 MeRIP-seq:(Medium) rs887075318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20497,RMVar_hsa_circ_75869,RMVar_hsa_circ_98559,RMVar_hsa_circ_187447,RMVar_hsa_circ_187448,RMVar_hsa_circ_342317 100683 RMVar_ID_100683 Human_SNP_ID_634146687 m1A Human chr17 - 80013576 80013576 80013576 CAGGTCTTGACGAGCCCTGCCCGGGCCGACGCATGCGGAGGATGGAAACACTTGCCCGGCAATGT CAGGTCTTGACGAGCCCTGCCCGGGCCGACGCGTGCGGAGGATGGAAACACTTGCCCGGCAATGT T C TBC1D16 Ensembl:ENSG00000167291 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:80013476..80013642 26863410 MeRIP-seq:(Medium) rs1016201216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464854,Human_RBP_ID_5467143 Human_Splice_Rec_1877058 RMVar_hsa_circ_20497,RMVar_hsa_circ_75869,RMVar_hsa_circ_98559,RMVar_hsa_circ_187447,RMVar_hsa_circ_187448,RMVar_hsa_circ_342317 100684 RMVar_ID_100684 Human_SNP_ID_634149627 m1A Human chr17 + 80024316 80024316 80024316 AGCACACACACCATAGACCCCACACCACGCACACCATAGACACACATACCACACACCACACACCA AGCACACACACCATAGACCCCACACCACGCACGCCATAGACACACATACCACACACCACACACCA A G AC116025.1 Ensembl:ENSG00000261978 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80024312..80024536 26863196 MeRIP-seq:(Medium) rs1283572446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200245 100685 RMVar_ID_100685 Human_SNP_ID_634149847 m1A Human chr17 + 80024616 80024616 80024616 ACCACACACCACACACCATAGACACACACACCACACACCATAAGCACACACACCACACACACCAT ACCACACACCACACACCATAGACACACACACCGCACACCATAAGCACACACACCACACACACCAT A G AC116025.1 Ensembl:ENSG00000261978 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80024304..80024639 26863196 MeRIP-seq:(Medium) rs1318995533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200248,Human_RBP_ID_26758496 100686 RMVar_ID_100686 Human_SNP_ID_634152960 m1A Human chr17 + 80035787 80035777 80035788 GACCCCGCCCCCGCGGCCCCGTCCGGGCCCCGATACCCACCCGGGTCCCGCTGCGGGGGCCGGAT GACCCCGCCCCCGCGGCCCCGTC___________ACCCACCCGGGTCCCGCTGCGGGGGCCGGAT CCGGGCCCCGAT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:80035776..80035875 26863410 MeRIP-seq:(Medium) rs1450162466 Functional Loss DEL dbSNP153 24..34 33 - - - 100687 RMVar_ID_100687 Human_SNP_ID_634152964 m1A Human chr17 + 80035787 80035787 80035787 GACCCCGCCCCCGCGGCCCCGTCCGGGCCCCGATACCCACCCGGGTCCCGCTGCGGGGGCCGGAT GACCCCGCCCCCGCGGCCCCGTCCGGGCCCCGGTACCCACCCGGGTCCCGCTGCGGGGGCCGGAT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:80035776..80035875 26863410 MeRIP-seq:(Medium) rs1027053482 Functional Loss SNV dbSNP153 33..33 33 - - - 100688 RMVar_ID_100688 Human_SNP_ID_634153306 m1A Human chr17 - 80036693 80036693 80036693 ACTCCAAGACCCGCTGCCCCTCGGCCCGGCTTACCGGCCCGCCGCGCCGCCCGGTTCCGCCATTT ACTCCAAGACCCGCTGCCCCTCGGCCCGGCTTCCCGGCCCGCCGCGCCGCCCGGTTCCGCCATTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80036686..80036757;chr17:80036665..80036761;chr17:80036674..80036829 26863196 MeRIP-seq:(Medium) rs752426610 Functional Loss SNV dbSNP153 33..33 33 - - - 100689 RMVar_ID_100689 Human_SNP_ID_634157453 m1A Human chr17 - 80050118 80050118 80050118 CTGCAGGTGTACCAGGTGCTGCTGCACCTCATAGAGATTCACCCCCAGCTCCTGCCGCTGGGCTC CTGCAGGTGTACCAGGTGCTGCTGCACCTCATGGAGATTCACCCCCAGCTCCTGCCGCTGGGCTC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:80050084..80050210 26863196 MeRIP-seq:(Medium) rs371604414 Functional Loss SNV dbSNP153 33..33 33 - - - 100690 RMVar_ID_100690 Human_SNP_ID_634157490 m1A Human chr17 + 80050184 80050184 80050184 AGCTGCTGGAGAAGAGTCACGACCGCCACGCAATGGCCTCGAGCGAGCGCAGGCAGAAGGAGGAG AGCTGCTGGAGAAGAGTCACGACCGCCACGCAGTGGCCTCGAGCGAGCGCAGGCAGAAGGAGGAG A G CCDC40 Ensembl:ENSG00000141519 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80050138..80050235 26863196 MeRIP-seq:(Medium) rs767636713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1877183,Human_Splice_Rec_1877217,Human_Splice_Rec_1877257,Human_Splice_Rec_1877277,Human_Splice_Rec_1877313 RMVar_hsa_circ_6677,RMVar_hsa_circ_268620,RMVar_hsa_circ_304611,RMVar_hsa_circ_333815,RMVar_hsa_circ_187450,RMVar_hsa_circ_27429,RMVar_hsa_circ_271103,RMVar_hsa_circ_337592,RMVar_hsa_circ_69624,RMVar_hsa_circ_187451,RMVar_hsa_circ_187452,RMVar_hsa_circ_265707,RMVar_hsa_circ_298235,RMVar_hsa_circ_56734,RMVar_hsa_circ_187454 100691 RMVar_ID_100691 Human_SNP_ID_634168083 m1A Human chr17 + 80087733 80087733 80087733 TAAAAACCGGTGCAGCTCGGAGGAGCTGGAGCAGAACAACCGGGTGACAGAGAATGAGTTCGTGC TAAAAACCGGTGCAGCTCGGAGGAGCTGGAGCCGAACAACCGGGTGACAGAGAATGAGTTCGTGC A C CCDC40 Ensembl:ENSG00000141519 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80087567..80087789 26863196 MeRIP-seq:(Medium) rs373825810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23753007 Human_Splice_Rec_1877199,Human_Splice_Rec_1877233,Human_Splice_Rec_1877329,Human_Splice_Rec_1877353,Human_Splice_Rec_1877359 RMVar_hsa_circ_187451,RMVar_hsa_circ_265707,RMVar_hsa_circ_78123,RMVar_hsa_circ_187456 100692 RMVar_ID_100692 Human_SNP_ID_634168084 m1A Human chr17 + 80087733 80087733 80087733 TAAAAACCGGTGCAGCTCGGAGGAGCTGGAGCAGAACAACCGGGTGACAGAGAATGAGTTCGTGC TAAAAACCGGTGCAGCTCGGAGGAGCTGGAGCGGAACAACCGGGTGACAGAGAATGAGTTCGTGC A G CCDC40 Ensembl:ENSG00000141519 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80087567..80087789 26863196 MeRIP-seq:(Medium) rs373825810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23753007 Human_Splice_Rec_1877199,Human_Splice_Rec_1877233,Human_Splice_Rec_1877329,Human_Splice_Rec_1877353,Human_Splice_Rec_1877359 RMVar_hsa_circ_187451,RMVar_hsa_circ_265707,RMVar_hsa_circ_78123,RMVar_hsa_circ_187456 100693 RMVar_ID_100693 Human_SNP_ID_634173746 m1A Human chr17 + 80104744 80104744 80104744 GAGTGGCTCCTCCCCAGTCCTGGAGGAGACTCACCCAGCTCACCAGCAGGGAGCCAGCAGACCAG GAGTGGCTCCTCCCCAGTCCTGGAGGAGACTCGCCCAGCTCACCAGCAGGGAGCCAGCAGACCAG A G GAA Ensembl:ENSG00000171298 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80104693..80104793 32194978 MeRIP-seq:(Medium) rs780554430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464863,Human_RBP_ID_22443964 RMVar_hsa_circ_9198 100694 RMVar_ID_100694 Human_SNP_ID_634173775 m1A Human chr17 + 80104798 80104798 80104798 CAGCAGACCAGGGCCCCGGGATGCCCAGGCACACCCCGGCCGTCCCAGAGCAGTGCCCACACAGT CAGCAGACCAGGGCCCCGGGATGCCCAGGCACGCCCCGGCCGTCCCAGAGCAGTGCCCACACAGT A G GAA Ensembl:ENSG00000171298 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:80104702..80104850 26863196 MeRIP-seq:(Medium) rs760205477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4456463,Human_RBP_ID_22443964 Clinvar_Rec_617 RMVar_hsa_circ_9198 100695 RMVar_ID_100695 Human_SNP_ID_634173840 m1A Human chr17 + 80104878 80104878 80104878 ACAGCCGCTTCGATTGCGCCCCTGACAAGGCCATCACCCAGGAACAGTGCGAGGCCCGCGGCTGT ACAGCCGCTTCGATTGCGCCCCTGACAAGGCCTTCACCCAGGAACAGTGCGAGGCCCGCGGCTGT A T GAA Ensembl:ENSG00000171298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80104742..80104881 26863196 MeRIP-seq:(Medium) rs745963730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26973283 RMVar_hsa_circ_9198 100696 RMVar_ID_100696 Human_SNP_ID_634176183 m1A Human chr17 + 80110729 80110729 80110729 GTCTCCCCACTGCAGCCTCTCGTTGTCCAGGTATGGCCCGGGTCCACTGCCTTCCCCGACTTCAC GTCTCCCCACTGCAGCCTCTCGTTGTCCAGGTGTGGCCCGGGTCCACTGCCTTCCCCGACTTCAC A G GAA Ensembl:ENSG00000171298 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80107841..80110735 32194978 MeRIP-seq:(Medium) rs1555600737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22543810 Human_Splice_Rec_1877390,Human_Splice_Rec_1877434 RMVar_hsa_circ_31888,RMVar_hsa_circ_64421 100697 RMVar_ID_100697 Human_SNP_ID_634176299 m1A Human chr17 + 80110993 80110993 80110993 CTTCATCAGGGGCTCTGAGGACGGCTGCCCCAACAATGAGCTGGAGAACCCACCCTACGTGCCTG CTTCATCAGGGGCTCTGAGGACGGCTGCCCCAGCAATGAGCTGGAGAACCCACCCTACGTGCCTG A G GAA Ensembl:ENSG00000171298 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80110943..80111037 26863196 MeRIP-seq:(Medium) rs1262434066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4456492 Human_Splice_Rec_1877392,Human_Splice_Rec_1877393,Human_Splice_Rec_1877436,Human_Splice_Rec_1877437,Human_Splice_Rec_1877455 RMVar_hsa_circ_31888,RMVar_hsa_circ_64421 100698 RMVar_ID_100698 Human_SNP_ID_634176469 m1A Human chr17 + 80111415 80111414 80111415 TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCAGGAATTACCAAGAAGAAGCATGGGGGTCAGGG TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGTGGGAATTACCAAGAAGAAGCATGGGGGTCAGGG CA TG GAA Ensembl:ENSG00000171298 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35614348 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_2524965,Human_RBP_ID_5365190,Human_RBP_ID_8232684,Human_RBP_ID_21974661,Human_RBP_ID_22500646 RMVar_hsa_circ_64421 100699 RMVar_ID_100699 Human_SNP_ID_634176472 m1A Human chr17 + 80111415 80111415 80111415 TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCAGGAATTACCAAGAAGAAGCATGGGGGTCAGGG TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCGGGAATTACCAAGAAGAAGCATGGGGGTCAGGG A G GAA Ensembl:ENSG00000171298 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7209921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2524965,Human_RBP_ID_5365190,Human_RBP_ID_8232684,Human_RBP_ID_21974661,Human_RBP_ID_22500646 RMVar_hsa_circ_64421 100700 RMVar_ID_100700 Human_SNP_ID_634176473 m1A Human chr17 + 80111415 80111415 80111415 TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCAGGAATTACCAAGAAGAAGCATGGGGGTCAGGG TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCTGGAATTACCAAGAAGAAGCATGGGGGTCAGGG A T GAA Ensembl:ENSG00000171298 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7209921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2524965,Human_RBP_ID_5365190,Human_RBP_ID_8232684,Human_RBP_ID_21974661,Human_RBP_ID_22500646 RMVar_hsa_circ_64421 100701 RMVar_ID_100701 Human_SNP_ID_634176482 m1A Human chr17 + 80111450 80111450 80111450 AATTACCAAGAAGAAGCATGGGGGTCAGGGGGATTCTGGCTGAACTGACCCAGCAGGATTCTTGC AATTACCAAGAAGAAGCATGGGGGTCAGGGGGCTTCTGGCTGAACTGACCCAGCAGGATTCTTGC A C GAA Ensembl:ENSG00000171298 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80111193..80111793 26863196 MeRIP-seq:(Medium) rs1021205791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5365190,Human_RBP_ID_18942351,Human_RBP_ID_21974661 RMVar_hsa_circ_64421 100702 RMVar_ID_100702 Human_SNP_ID_634176515 m1A Human chr17 + 80111610 80111607 80111610 TTTACAAGGAAGTACAAGGATGGGCCTGGGAGAAGGTTTGGGGGCCTGAGGCTATAGTTTGGCCC TTTACAAGGAAGTACAAGGATGGGCCTGGG___AGGTTTGGGGGCCTGAGGCTATAGTTTGGCCC GAGA G GAA Ensembl:ENSG00000171298 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80111516..80111778 26863196 MeRIP-seq:(Medium) rs1199100203 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_13186277 RMVar_hsa_circ_64421 100703 RMVar_ID_100703 Human_SNP_ID_634177330 m1A Human chr17 - 80113363 80113363 80113363 GGGCCACCGCCCCTGCCTAGGTCACTCACTCCAGGAAGAGGGGCCGGGCCACGGTCTCCCCCGCG GGGCCACCGCCCCTGCCTAGGTCACTCACTCCGGGAAGAGGGGCCGGGCCACGGTCTCCCCCGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80112618..80116847 32194978 MeRIP-seq:(Medium) rs1263308515 Functional Loss SNV dbSNP153 33..33 33 - - - 100704 RMVar_ID_100704 Human_SNP_ID_634179270 m1A Human chr17 - 80119419 80119419 80119419 GTGCCCAGCTCCAGGTGACACATGCAACCCCCAGGCCCGCACACAGCTGCTGCCCGCACACAGGC GTGCCCAGCTCCAGGTGACACATGCAACCCCCCGGCCCGCACACAGCTGCTGCCCGCACACAGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80116951..80119475 32194978 MeRIP-seq:(Medium) rs1041120127 Functional Loss SNV dbSNP153 33..33 33 - - - 100705 RMVar_ID_100705 Human_SNP_ID_634185119 m1A Human chr17 - 80140026 80140026 80140026 AGCTGGATTACGGACAGCATGTTGTCGCGGGCACTCCAGGGCGTGTTTTTGGTAAGCACTTTTGT AGCTGGATTACGGACAGCATGTTGTCGCGGGCTCTCCAGGGCGTGTTTTTGGTAAGCACTTTTGT T A EIF4A3 Ensembl:ENSG00000141543 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:80139475..80140075 32194978 MeRIP-seq:(Medium) rs372677327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1010978,Human_RBP_ID_1544008,Human_RBP_ID_1870349,Human_RBP_ID_4456608,Human_RBP_ID_6649799,Human_RBP_ID_8823070,Human_RBP_ID_13186697,Human_RBP_ID_18439814,Human_RBP_ID_19080294,Human_RBP_ID_22445794,Human_RBP_ID_23753065 Human_Splice_Rec_1877487,Human_Splice_Rec_1877521,Human_Splice_Rec_1877541,Human_Splice_Rec_1877557 RMVar_hsa_circ_187458,RMVar_hsa_circ_344364,RMVar_hsa_circ_107124,RMVar_hsa_circ_187461,RMVar_hsa_circ_83461,RMVar_hsa_circ_187462,RMVar_hsa_circ_345039,RMVar_hsa_circ_11156,RMVar_hsa_circ_187464,RMVar_hsa_circ_55970,RMVar_hsa_circ_366758,RMVar_hsa_circ_187465,RMVar_hsa_circ_10014,RMVar_hsa_circ_113094,RMVar_hsa_circ_370962,RMVar_hsa_circ_187466 100706 RMVar_ID_100706 Human_SNP_ID_634185576 m1A Human chr17 - 80141689 80141689 80141689 CTGTAACTACAGTGTTCAAAAAGTACAATTTAAAATTTTCTAGTATGTATTGACTCAGCAAATTT CTGTAACTACAGTGTTCAAAAAGTACAATTTACAATTTTCTAGTATGTATTGACTCAGCAAATTT T G EIF4A3 Ensembl:ENSG00000141543 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:80140461..80141766 32194978 MeRIP-seq:(Medium) rs929860483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17609271,Human_RBP_ID_25329241 RMVar_hsa_circ_55970,RMVar_hsa_circ_366758,RMVar_hsa_circ_187465,RMVar_hsa_circ_370962,RMVar_hsa_circ_187467,RMVar_hsa_circ_295833,RMVar_hsa_circ_296500,RMVar_hsa_circ_187468 100707 RMVar_ID_100707 Human_SNP_ID_634187176 m1A Human chr17 - 80147062 80147062 80147062 AGCGGCACAGCGAGGTCGGCAGCGGCACAGCGAGGTCGGCAGCGGCAGCGAGGTCGGCAGCGGCA AGCGGCACAGCGAGGTCGGCAGCGGCACAGCGGGGTCGGCAGCGGCAGCGAGGTCGGCAGCGGCA T C EIF4A3 Ensembl:ENSG00000141543 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:80146826..80147150 26863410 MeRIP-seq:(Medium) rs1436758808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132726,Human_RBP_ID_767086,Human_RBP_ID_9379199 Human_Splice_Rec_1877511 100708 RMVar_ID_100708 Human_SNP_ID_634195750 m1A Human chr17 - 80179077 80179077 80179077 TGTATGCTAAAAATACTTGAAAATCAGAGCAAATCAACACCTGTCATCTGAAAAATGGAAAATGG TGTATGCTAAAAATACTTGAAAATCAGAGCAATTCAACACCTGTCATCTGAAAAATGGAAAATGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80179072..80179207 26863196 MeRIP-seq:(Medium) rs1010142926 Functional Loss SNV dbSNP153 33..33 33 - - - 100709 RMVar_ID_100709 Human_SNP_ID_634198744 m1A Human chr17 - 80189832 80189832 80189832 GCTGCCTCTCGGCAGCCACGGCCCGCTCCCGCAGCGAGTGGATGCGCTCCACCAGCTCCTGTCGG GCTGCCTCTCGGCAGCCACGGCCCGCTCCCGCGGCGAGTGGATGCGCTCCACCAGCTCCTGTCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80189782..80189868 26863196 MeRIP-seq:(Medium) rs778718425 Functional Loss SNV dbSNP153 33..33 33 - - - 100710 RMVar_ID_100710 Human_SNP_ID_634205421 m1A Human chr17 - 80210822 80210822 80210822 GGTCACCATGTCCTACCCCATGCGCTCCGTGCAGCACCGGCACTTCCGCCTCGTGCACAACCTCA GGTCACCATGTCCTACCCCATGCGCTCCGTGCGGCACCGGCACTTCCGCCTCGTGCACAACCTCA T C SGSH Ensembl:ENSG00000181523 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80210678..80210850 26863196 MeRIP-seq:(Medium) rs144143780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502046,Human_RBP_ID_22761745 Human_miRNA_ID_2515939 Clinvar_Rec_618 GWAS_ID_13193 RMVar_hsa_circ_75752,RMVar_hsa_circ_187470 100711 RMVar_ID_100711 Human_SNP_ID_634207660 m1A Human chr17 - 80217142 80217142 80217142 AGAGTGGCGCGTACAACAACAGCGCCATCGCCACCCCGCACCTGGACGCCTTGGCCCGCCGCAGC AGAGTGGCGCGTACAACAACAGCGCCATCGCCCCCCCGCACCTGGACGCCTTGGCCCGCCGCAGC T G SGSH Ensembl:ENSG00000181523 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80217091..80217175 26863196 MeRIP-seq:(Medium) rs962142186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27458375 Human_Splice_Rec_1878126,Human_Splice_Rec_1878140,Human_Splice_Rec_1878148,Human_Splice_Rec_1878164,Human_Splice_Rec_1878176,Human_Splice_Rec_1878184,Human_Splice_Rec_1878194,Human_Splice_Rec_1878202,Human_Splice_Rec_1878208,Human_Splice_Rec_1878216,Human_Splice_Rec_1878224,Human_Splice_Rec_1878230,Human_Splice_Rec_1878234 RMVar_hsa_circ_75752,RMVar_hsa_circ_187470 100712 RMVar_ID_100712 Human_SNP_ID_634207800 m1A Human chr17 + 80217629 80217626 80217630 TGGCAGGTGAGCATGGTATGGAGGCTGGACTGATTGATAGATGGTGGGTATGTTGGCAGGTGAGC TGGCAGGTGAGCATGGTATGGAGGCTGGAC____TGATAGATGGTGGGTATGTTGGCAGGTGAGC CTGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80217610..80217703 26863196 MeRIP-seq:(Medium) rs58759630 Functional Loss DEL dbSNP153 31..34 33 - - - 100713 RMVar_ID_100713 Human_SNP_ID_634207801 m1A Human chr17 + 80217629 80217629 80217629 TGGCAGGTGAGCATGGTATGGAGGCTGGACTGATTGATAGATGGTGGGTATGTTGGCAGGTGAGC TGGCAGGTGAGCATGGTATGGAGGCTGGACTGGTTGATAGATGGTGGGTATGTTGGCAGGTGAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80217610..80217703 26863196 MeRIP-seq:(Medium) rs1567929310 Functional Loss SNV dbSNP153 33..33 33 - - - 100714 RMVar_ID_100714 Human_SNP_ID_634208495 m1A Human chr17 + 80220279 80220279 80220279 GGGGACGCGCCCGGCAGAGCCCCAGGACTAGCAGCAGCGCGCAGCAGGCGGGCACGGGGCAGCTC GGGGACGCGCCCGGCAGAGCCCCAGGACTAGCCGCAGCGCGCAGCAGGCGGGCACGGGGCAGCTC A C SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80220204..80220309 26863196 MeRIP-seq:(Medium) rs1359433732 Functional Loss SNV dbSNP153 33..33 33 - - - 100715 RMVar_ID_100715 Human_SNP_ID_634208504 m1A Human chr17 + 80220289 80220289 80220289 CCGGCAGAGCCCCAGGACTAGCAGCAGCGCGCAGCAGGCGGGCACGGGGCAGCTCATGGCGGCGG CCGGCAGAGCCCCAGGACTAGCAGCAGCGCGCTGCAGGCGGGCACGGGGCAGCTCATGGCGGCGG A T SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80220182..80220350 26863196 MeRIP-seq:(Medium) rs1400013703 Functional Loss SNV dbSNP153 33..33 33 - - - 100716 RMVar_ID_100716 Human_SNP_ID_634209893 m1A Human chr17 + 80224202 80224196 80224202 AGTGTGTGTGAGAGTGTGTATGAGTGTGTGTGAGTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA AGTGTGTGTGAGAGTGTGTATGAGTGT______GTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA TGTGTGA T SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80224097..80224522 26863196 MeRIP-seq:(Medium) rs1221283782 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_23753144 RMVar_hsa_circ_80111,RMVar_hsa_circ_276253,RMVar_hsa_circ_187474,RMVar_hsa_circ_309753,RMVar_hsa_circ_187476 100717 RMVar_ID_100717 Human_SNP_ID_634209895 m1A Human chr17 + 80224202 80224198 80224202 AGTGTGTGTGAGAGTGTGTATGAGTGTGTGTGAGTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA AGTGTGTGTGAGAGTGTGTATGAGTGTGT____GTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA TGTGA T SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80224097..80224522 26863196 MeRIP-seq:(Medium) rs1279464041 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23753144 RMVar_hsa_circ_80111,RMVar_hsa_circ_276253,RMVar_hsa_circ_187474,RMVar_hsa_circ_309753,RMVar_hsa_circ_187476 100718 RMVar_ID_100718 Human_SNP_ID_634209901 m1A Human chr17 + 80224202 80224200 80224202 AGTGTGTGTGAGAGTGTGTATGAGTGTGTGTGAGTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA AGTGTGTGTGAGAGTGTGTATGAGTGTGTGT__GTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA TGA T SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80224097..80224522 26863196 MeRIP-seq:(Medium) rs10577282 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23753144 RMVar_hsa_circ_80111,RMVar_hsa_circ_276253,RMVar_hsa_circ_187474,RMVar_hsa_circ_309753,RMVar_hsa_circ_187476 100719 RMVar_ID_100719 Human_SNP_ID_634209904 m1A Human chr17 + 80224202 80224202 80224202 AGTGTGTGTGAGAGTGTGTATGAGTGTGTGTGAGTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA AGTGTGTGTGAGAGTGTGTATGAGTGTGTGTGTGTGTGTGAATGAGTGAGTGTGTGAGAGTGTGA A T SLC26A11 Ensembl:ENSG00000181045 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80224097..80224522 26863196 MeRIP-seq:(Medium) rs28672688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23753144 RMVar_hsa_circ_80111,RMVar_hsa_circ_276253,RMVar_hsa_circ_187474,RMVar_hsa_circ_309753,RMVar_hsa_circ_187476 100720 RMVar_ID_100720 Human_SNP_ID_634209937 m1A Human chr17 - 80224241 80224241 80224241 CTCACACACGCACACACTCACACACTCCCTCAAACCCACTCACACTCTCACACACTCACTCATTC CTCACACACGCACACACTCACACACTCCCTCACACCCACTCACACTCTCACACACTCACTCATTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80224196..80224425 26863196 MeRIP-seq:(Medium) rs1351377477 Functional Loss SNV dbSNP153 33..33 33 - - - 100721 RMVar_ID_100721 Human_SNP_ID_634209966 m1A Human chr17 - 80224266 80224264 80224266 GCACACTCACTCACACACGCACTCACTCACACACGCACACACTCACACACTCCCTCAAACCCACT GCACACTCACTCACACACGCACTCACTCACAC__GCACACACTCACACACTCCCTCAAACCCACT CGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:80224176..80224369 26863196 MeRIP-seq:(Medium) rs898416000 Functional Loss DEL dbSNP153 33..34 33 - - - 100722 RMVar_ID_100722 Human_SNP_ID_634210086 m1A Human chr17 - 80224328 80224328 80224328 TCACACCCACACCCACTCTCACACTCTCACTCATACACACTCACACTCTCTCACACACACACGCA TCACACCCACACCCACTCTCACACTCTCACTCGTACACACTCACACTCTCTCACACACACACGCA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:80224158..80224441 26863196 MeRIP-seq:(Medium) rs963740896 Functional Loss SNV dbSNP153 33..33 33 - - - 100723 RMVar_ID_100723 Human_SNP_ID_634210129 m1A Human chr17 - 80224366 80224364 80224366 TCATACACTCACACACGCGCGCGCGCACTCACACTCCCTCACACCCACACCCACTCTCACACTCT TCATACACTCACACACGCGCGCGCGCACTCAC__TCCCTCACACCCACACCCACTCTCACACTCT AGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80224096..80224524 26863196 MeRIP-seq:(Medium) rs148238632 Functional Loss DEL dbSNP153 33..34 33 - - - 100724 RMVar_ID_100724 Human_SNP_ID_634210133 m1A Human chr17 - 80224366 80224366 80224366 TCATACACTCACACACGCGCGCGCGCACTCACACTCCCTCACACCCACACCCACTCTCACACTCT TCATACACTCACACACGCGCGCGCGCACTCACGCTCCCTCACACCCACACCCACTCTCACACTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80224096..80224524 26863196 MeRIP-seq:(Medium) rs1344973434 Functional Loss SNV dbSNP153 33..33 33 - - - 100725 RMVar_ID_100725 Human_SNP_ID_634221110 m1A Human chr17 + 80260901 80260901 80260901 AGCGCGCGGCAGGCGGCGAGCTCGGGGGCCGCAGGTGCGAGCGGGCCTGGAGAGTCTCCCGGGGC AGCGCGCGGCAGGCGGCGAGCTCGGGGGCCGCGGGTGCGAGCGGGCCTGGAGAGTCTCCCGGGGC A G RNF213 Ensembl:ENSG00000173821 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80260850..80261017 26863196 MeRIP-seq:(Medium) rs1416692727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5319314,Human_RBP_ID_18460485,Human_RBP_ID_19084278 Human_Splice_Rec_1878447,Human_Splice_Rec_1878581,Human_Splice_Rec_1878713 100726 RMVar_ID_100726 Human_SNP_ID_634225406 m1A Human chr17 - 80274866 80274861 80274866 ACACACACACATCCCATTCACACCACTCACACACCCCCCAACACACACCCCACTCACCCCCCACT ACACACACACATCCCATTCACACCACTCACAC_____CCAACACACACCCCACTCACCCCCCACT GGGGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80274860..80275217 26863196 MeRIP-seq:(Medium) rs1297372405 Functional Loss DEL dbSNP153 33..37 33 - - - 100727 RMVar_ID_100727 Human_SNP_ID_634225407 m1A Human chr17 - 80274866 80274864 80274866 ACACACACACATCCCATTCACACCACTCACACACCCCCCAACACACACCCCACTCACCCCCCACT ACACACACACATCCCATTCACACCACTCACAC__CCCCCAACACACACCCCACTCACCCCCCACT GGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80274860..80275217 26863196 MeRIP-seq:(Medium) rs1366943259 Functional Loss DEL dbSNP153 33..34 33 - - - 100728 RMVar_ID_100728 Human_SNP_ID_634225410 m1A Human chr17 - 80274866 80274866 80274866 ACACACACACATCCCATTCACACCACTCACACACCCCCCAACACACACCCCACTCACCCCCCACT ACACACACACATCCCATTCACACCACTCACACCCCCCCCAACACACACCCCACTCACCCCCCACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80274860..80275217 26863196 MeRIP-seq:(Medium) rs1385738929 Functional Loss SNV dbSNP153 33..33 33 - - - 100729 RMVar_ID_100729 Human_SNP_ID_634225458 m1A Human chr17 - 80274929 80274927 80274929 ACACACCCCCCACTCACACACCCAACACACACACCCCACTCACACCCCACTCACACACCCCCAAC ACACACCCCCCACTCACACACCCAACACACAC__CCCACTCACACCCCACTCACACACCCCCAAC GGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80274927..80275157 26863196 MeRIP-seq:(Medium) rs1199505563 Functional Loss DEL dbSNP153 33..34 33 - - - 100730 RMVar_ID_100730 Human_SNP_ID_634225463 m1A Human chr17 - 80274929 80274929 80274929 ACACACCCCCCACTCACACACCCAACACACACACCCCACTCACACCCCACTCACACACCCCCAAC ACACACCCCCCACTCACACACCCAACACACACCCCCCACTCACACCCCACTCACACACCCCCAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80274927..80275157 26863196 MeRIP-seq:(Medium) rs1291392941 Functional Loss SNV dbSNP153 33..33 33 - - - 100731 RMVar_ID_100731 Human_SNP_ID_634227269 m1A Human chr17 + 80280840 80280840 80280840 CTTAACAGATGTGAGGAGGAGAAATGGATGGGAGATTTATAGTAAAGCTGTCAACGTACACGGGT CTTAACAGATGTGAGGAGGAGAAATGGATGGGCGATTTATAGTAAAGCTGTCAACGTACACGGGT A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80280837..80281052 26863196 MeRIP-seq:(Medium) rs1170870205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200260,Human_RBP_ID_5237720,Human_RBP_ID_8941860,Human_RBP_ID_9423656 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447 100732 RMVar_ID_100732 Human_SNP_ID_634227272 m1A Human chr17 - 80280843 80280842 80280843 TCCACCCGTGTACGTTGACAGCTTTACTATAAATCTCCCATCCATTTCTCCTCCTCACATCTGTT TCCACCCGTGTACGTTGACAGCTTTACTATAA_TCTCCCATCCATTTCTCCTCCTCACATCTGTT AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80280837..80281108 26863196 MeRIP-seq:(Medium) rs1285390266 Functional Loss DEL dbSNP153 33..33 33 - - - 100733 RMVar_ID_100733 Human_SNP_ID_634227612 m1A Human chr17 + 80281486 80281482 80281486 ACCCCACTCACAACACTCACACACCCCCCAACATACATACACCCCACTCACACACACACCCCAAC ACCCCACTCACAACACTCACACACCCCCC____TACATACACCCCACTCACACACACACCCCAAC CAACA C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80281482..80281679 26863196 MeRIP-seq:(Medium) rs1352625988 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_200267,Human_RBP_ID_262757,Human_RBP_ID_2525086,Human_RBP_ID_24532037 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447 100734 RMVar_ID_100734 Human_SNP_ID_634227614 m1A Human chr17 + 80281486 80281483 80281487 ACCCCACTCACAACACTCACACACCCCCCAACATACATACACCCCACTCACACACACACCCCAAC ACCCCACTCACAACACTCACACACCCCCCA____ACATACACCCCACTCACACACACACCCCAAC AACAT A RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80281482..80281679 26863196 MeRIP-seq:(Medium) rs1297218760 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_200267,Human_RBP_ID_262757,Human_RBP_ID_2525086,Human_RBP_ID_24532037 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447 100735 RMVar_ID_100735 Human_SNP_ID_634227616 m1A Human chr17 + 80281486 80281485 80281487 ACCCCACTCACAACACTCACACACCCCCCAACATACATACACCCCACTCACACACACACCCCAAC ACCCCACTCACAACACTCACACACCCCCCAAC__ACATACACCCCACTCACACACACACCCCAAC CAT C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80281482..80281679 26863196 MeRIP-seq:(Medium) rs1279120467 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_200267,Human_RBP_ID_262757,Human_RBP_ID_2525086,Human_RBP_ID_24532037 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447 100736 RMVar_ID_100736 Human_SNP_ID_634230162 m1A Human chr17 + 80289753 80289753 80289753 ACAAGGGGAGCCTGAAGACCTCAAGAAGCCAGAGGGGAAGAACAGAAGTGCAGCTGCTGTGAAAA ACAAGGGGAGCCTGAAGACCTCAAGAAGCCAGCGGGGAAGAACAGAAGTGCAGCTGCTGTGAAAA A C RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80289706..80289832 26863196 MeRIP-seq:(Medium) rs779148717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_201721,Human_RBP_ID_822601,Human_RBP_ID_3951232,Human_RBP_ID_5525957,Human_RBP_ID_5577871,Human_RBP_ID_9289383,Human_RBP_ID_9377013,Human_RBP_ID_19080314,Human_RBP_ID_24544953,Human_RBP_ID_26330908,Human_RBP_ID_27813192 Human_Splice_Rec_1878458,Human_Splice_Rec_1878459,Human_Splice_Rec_1878590,Human_Splice_Rec_1878591,Human_Splice_Rec_1878722,Human_Splice_Rec_1878723,Human_Splice_Rec_1878748,Human_Splice_Rec_1878749,Human_Splice_Rec_1878783 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_56827,RMVar_hsa_circ_115807,RMVar_hsa_circ_358836,RMVar_hsa_circ_361607,RMVar_hsa_circ_367356,RMVar_hsa_circ_354762,RMVar_hsa_circ_308241,RMVar_hsa_circ_358062,RMVar_hsa_circ_187486,RMVar_hsa_circ_357230,RMVar_hsa_circ_292602,RMVar_hsa_circ_187487,RMVar_hsa_circ_187488 100737 RMVar_ID_100737 Human_SNP_ID_634230163 m1A Human chr17 + 80289753 80289753 80289753 ACAAGGGGAGCCTGAAGACCTCAAGAAGCCAGAGGGGAAGAACAGAAGTGCAGCTGCTGTGAAAA ACAAGGGGAGCCTGAAGACCTCAAGAAGCCAGGGGGGAAGAACAGAAGTGCAGCTGCTGTGAAAA A G RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80289706..80289832 26863196 MeRIP-seq:(Medium) rs779148717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_201721,Human_RBP_ID_822601,Human_RBP_ID_3951232,Human_RBP_ID_5525957,Human_RBP_ID_5577871,Human_RBP_ID_9289383,Human_RBP_ID_9377013,Human_RBP_ID_19080314,Human_RBP_ID_24544953,Human_RBP_ID_26330908,Human_RBP_ID_27813192 Human_Splice_Rec_1878458,Human_Splice_Rec_1878459,Human_Splice_Rec_1878590,Human_Splice_Rec_1878591,Human_Splice_Rec_1878722,Human_Splice_Rec_1878723,Human_Splice_Rec_1878748,Human_Splice_Rec_1878749,Human_Splice_Rec_1878783 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_56827,RMVar_hsa_circ_115807,RMVar_hsa_circ_358836,RMVar_hsa_circ_361607,RMVar_hsa_circ_367356,RMVar_hsa_circ_354762,RMVar_hsa_circ_308241,RMVar_hsa_circ_358062,RMVar_hsa_circ_187486,RMVar_hsa_circ_357230,RMVar_hsa_circ_292602,RMVar_hsa_circ_187487,RMVar_hsa_circ_187488 100738 RMVar_ID_100738 Human_SNP_ID_634230636 m1A Human chr17 + 80290526 80290526 80290526 TGTGCGCGTGTGTGCATGCACATGGCAGGTGGACAGATCTCACGGGAATCAGATTTCTGTTTTGG TGTGCGCGTGTGTGCATGCACATGGCAGGTGGCCAGATCTCACGGGAATCAGATTTCTGTTTTGG A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80290525..80290648 26863196 MeRIP-seq:(Medium) rs1389163252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648642,Human_RBP_ID_22660594,Human_RBP_ID_23114339 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_56827,RMVar_hsa_circ_115807,RMVar_hsa_circ_358836,RMVar_hsa_circ_361607,RMVar_hsa_circ_367356,RMVar_hsa_circ_354762,RMVar_hsa_circ_308241,RMVar_hsa_circ_358062,RMVar_hsa_circ_187486,RMVar_hsa_circ_357230,RMVar_hsa_circ_292602,RMVar_hsa_circ_187487,RMVar_hsa_circ_187488 100739 RMVar_ID_100739 Human_SNP_ID_634230640 m1A Human chr17 + 80290530 80290530 80290530 CGCGTGTGTGCATGCACATGGCAGGTGGACAGATCTCACGGGAATCAGATTTCTGTTTTGGTTTT CGCGTGTGTGCATGCACATGGCAGGTGGACAGCTCTCACGGGAATCAGATTTCTGTTTTGGTTTT A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80290527..80290682 26863196 MeRIP-seq:(Medium) rs764487227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648642,Human_RBP_ID_22660594,Human_RBP_ID_23114339 RMVar_hsa_circ_57813,RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_56827,RMVar_hsa_circ_115807,RMVar_hsa_circ_358836,RMVar_hsa_circ_361607,RMVar_hsa_circ_367356,RMVar_hsa_circ_354762,RMVar_hsa_circ_308241,RMVar_hsa_circ_358062,RMVar_hsa_circ_187486,RMVar_hsa_circ_357230,RMVar_hsa_circ_292602,RMVar_hsa_circ_187487,RMVar_hsa_circ_187488 100740 RMVar_ID_100740 Human_SNP_ID_634231910 m1A Human chr17 + 80294810 80294810 80294810 CATGAACCACATCACAGACGGGCCGAGGAAGGACCTGGTGAAGGGGAAGCAGATTGCCGCTGCGC CATGAACCACATCACAGACGGGCCGAGGAAGGGCCTGGTGAAGGGGAAGCAGATTGCCGCTGCGC A G RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80294760..80294850 26863196 MeRIP-seq:(Medium) rs867744222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131861,Human_RBP_ID_897996,Human_RBP_ID_5185721,Human_RBP_ID_5577874,Human_RBP_ID_9289385,Human_RBP_ID_9377017,Human_RBP_ID_18989445 Human_Splice_Rec_1878464,Human_Splice_Rec_1878596,Human_Splice_Rec_1878728,Human_Splice_Rec_1878754 RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_9447,RMVar_hsa_circ_11022,RMVar_hsa_circ_56827,RMVar_hsa_circ_115807,RMVar_hsa_circ_358836,RMVar_hsa_circ_361607,RMVar_hsa_circ_367356,RMVar_hsa_circ_358062,RMVar_hsa_circ_187486,RMVar_hsa_circ_357230,RMVar_hsa_circ_339933,RMVar_hsa_circ_74205,RMVar_hsa_circ_351719,RMVar_hsa_circ_354181,RMVar_hsa_circ_359749,RMVar_hsa_circ_351683,RMVar_hsa_circ_337251,RMVar_hsa_circ_339060,RMVar_hsa_circ_64952 100741 RMVar_ID_100741 Human_SNP_ID_634239079 m1A Human chr17 - 80315698 80315687 80315699 CCAGTACCTCCACCATCACTTCCATTACCTCTACCATCACCTTCACCACCACCATCACCTCCAGT CCAGTACCTCCACCATCACTTCCATTACCTC____________CACCACCACCATCACCTCCAGT GAAGGTGATGGTA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80315652..80315735 26863196 MeRIP-seq:(Medium) rs1228614661 Functional Loss DEL dbSNP153 32..43 33 - - - 100742 RMVar_ID_100742 Human_SNP_ID_634239273 m1A Human chr17 - 80315920 80315910 80315920 CCACCAGCATCACCACTGTCACCTCCACCACCACCACCTCCATCACCACCATCACCTTCACCACC CCACCAGCATCACCACTGTCACCTCCACCACC__________TCACCACCATCACCTTCACCACC ATGGAGGTGGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80315910..80315975 26863196 MeRIP-seq:(Medium) rs1157794570 Functional Loss DEL dbSNP153 33..42 33 - - - 100743 RMVar_ID_100743 Human_SNP_ID_634239279 m1A Human chr17 - 80315917 80315914 80315917 CCAGCATCACCACTGTCACCTCCACCACCACCACCTCCATCACCACCATCACCTTCACCACCACC CCAGCATCACCACTGTCACCTCCACCACCACC___TCCATCACCACCATCACCTTCACCACCACC AGGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80315914..80316046 26863196 MeRIP-seq:(Medium) rs1224833235 Functional Loss DEL dbSNP153 33..35 33 - - - 100744 RMVar_ID_100744 Human_SNP_ID_634239281 m1A Human chr17 - 80315917 80315917 80315917 CCAGCATCACCACTGTCACCTCCACCACCACCACCTCCATCACCACCATCACCTTCACCACCACC CCAGCATCACCACTGTCACCTCCACCACCACCGCCTCCATCACCACCATCACCTTCACCACCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80315914..80316046 26863196 MeRIP-seq:(Medium) rs1313542316 Functional Loss SNV dbSNP153 33..33 33 - - - 100745 RMVar_ID_100745 Human_SNP_ID_634247566 m1A Human chr17 + 80345482 80345482 80345482 AGAAACTTGAGAGGCTCTGCCTGACCTTAGGGATCCCCCAGGCCACCGACCCCGACAAAACGTAT AGAAACTTGAGAGGCTCTGCCTGACCTTAGGGGTCCCCCAGGCCACCGACCCCGACAAAACGTAT A G RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:80345376..80345550 26863196 MeRIP-seq:(Medium) rs745547008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766214,Human_RBP_ID_5526009,Human_RBP_ID_8825024,Human_RBP_ID_9258045,Human_RBP_ID_9289441,Human_RBP_ID_22061753 RMVar_hsa_circ_40321,RMVar_hsa_circ_56827,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_54503,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_64207,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_55918,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_357755,RMVar_hsa_circ_105315,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_375345,RMVar_hsa_circ_187508,RMVar_hsa_circ_187510 100746 RMVar_ID_100746 Human_SNP_ID_634250192 m1A Human chr17 + 80353588 80353579 80353588 GAGACGGAGGCCAGCACATCAGGGGAGGTGGCAGAGGTGGCAGAGGAGGCCATGGAAACAGAAAG GAGACGGAGGCCAGCACATCAGGG_________GAGGTGGCAGAGGAGGCCATGGAAACAGAAAG GGAGGTGGCA G RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80353501..80353675 26863196 MeRIP-seq:(Medium) rs746722534 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_820357,Human_RBP_ID_3951260,Human_RBP_ID_8825039,Human_RBP_ID_9289461,Human_RBP_ID_18989456,Human_RBP_ID_22959291,Human_RBP_ID_26332520 Human_Splice_Rec_1878514,Human_Splice_Rec_1878515,Human_Splice_Rec_1878646,Human_Splice_Rec_1878647 RMVar_hsa_circ_4887,RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_372766,RMVar_hsa_circ_41736,RMVar_hsa_circ_187512 100747 RMVar_ID_100747 Human_SNP_ID_634250988 m1A Human chr17 - 80355475 80355475 80355475 CGGTCACCCCGCTTCTTCCTCTGTGAGCCCCCATTCCCGGTCACCCCTCTTCCTCCGTGAGCCCC CGGTCACCCCGCTTCTTCCTCTGTGAGCCCCCCTTCCCGGTCACCCCTCTTCCTCCGTGAGCCCC T G RNF213-AS1 Ensembl:ENSG00000263069 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80355397..80355575 26863196 MeRIP-seq:(Medium) rs1295509255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18942359 100748 RMVar_ID_100748 Human_SNP_ID_634251201 m1A Human chr17 + 80355729 80355655 80355729 AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGACGGGAATGGGGGCTCACGGAGGAAGAAGCGGG _________________________________CGGGAATGGGGGCTCACGGAGGAAGAAGCGGG CGGGAATGGGGGCTTACAGGGGGAAGAAGCGGGGTGACCGGGAATGGGGGCTTACAGAGGAAGAAGCGGGGTGGA C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80355718..80355794;chr17:80355721..80355812 26863196 MeRIP-seq:(Medium) rs1568123705 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_8192437,Human_RBP_ID_9423661 RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_41736,RMVar_hsa_circ_43555 100749 RMVar_ID_100749 Human_SNP_ID_634251235 m1A Human chr17 + 80355729 80355692 80355729 AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGACGGGAATGGGGGCTCACGGAGGAAGAAGCGGG _________________________________CGGGAATGGGGGCTCACGGAGGAAGAAGCGGG CCGGGAATGGGGGCTTACAGAGGAAGAAGCGGGGTGGA C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80355718..80355794;chr17:80355721..80355812 26863196 MeRIP-seq:(Medium) rs1568123877 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_8192437,Human_RBP_ID_9423661 RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_41736,RMVar_hsa_circ_43555 100750 RMVar_ID_100750 Human_SNP_ID_634251243 m1A Human chr17 + 80355729 80355699 80355730 AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGACGGGAATGGGGGCTCACGGAGGAAGAAGCGGG AAT_______________________________GGGAATGGGGGCTCACGGAGGAAGAAGCGGG TGGGGGCTTACAGAGGAAGAAGCGGGGTGGAC T RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80355718..80355794;chr17:80355721..80355812 26863196 MeRIP-seq:(Medium) rs1488340791 Functional Loss DEL dbSNP153 4..34 33 - - - Human_RBP_ID_8192437,Human_RBP_ID_9423661 RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_41736,RMVar_hsa_circ_43555 100751 RMVar_ID_100751 Human_SNP_ID_634251279 m1A Human chr17 + 80355729 80355729 80355729 AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGACGGGAATGGGGGCTCACGGAGGAAGAAGCGGG AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGCCGGGAATGGGGGCTCACGGAGGAAGAAGCGGG A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80355718..80355794;chr17:80355721..80355812 26863196 MeRIP-seq:(Medium) rs1293232376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8192437,Human_RBP_ID_9423661 RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_41736,RMVar_hsa_circ_43555 100752 RMVar_ID_100752 Human_SNP_ID_634251280 m1A Human chr17 + 80355729 80355729 80355729 AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGACGGGAATGGGGGCTCACGGAGGAAGAAGCGGG AATGGGGGCTTACAGAGGAAGAAGCGGGGTGGGCGGGAATGGGGGCTCACGGAGGAAGAAGCGGG A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:80355718..80355794;chr17:80355721..80355812 26863196 MeRIP-seq:(Medium) rs1293232376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8192437,Human_RBP_ID_9423661 RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_41736,RMVar_hsa_circ_43555 100753 RMVar_ID_100753 Human_SNP_ID_634265450 m1A Human chr17 + 80401246 80401246 80401246 CAGCTCGCTCCCCGCCAGGCTGATCAGGCTCCAGCTCTTCTTCAGCCTCTGCTCCCCACCCTATA CAGCTCGCTCCCCGCCAGGCTGATCAGGCTCCCGCTCTTCTTCAGCCTCTGCTCCCCACCCTATA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80401069..80401297 26863196 MeRIP-seq:(Medium) rs1382296316 Functional Loss SNV dbSNP153 33..33 33 - - - 100754 RMVar_ID_100754 Human_SNP_ID_634284795 m1A Human chr17 - 80467976 80467976 80467976 GGCAGTGTTTGCTTTTGCCGAGCTGGTGTCCGACAGCTCCCTGGGTGTCCGGGGTGGGAGAGCTG GGCAGTGTTTGCTTTTGCCGAGCTGGTGTCCGTCAGCTCCCTGGGTGTCCGGGGTGGGAGAGCTG T A NPTX1 Ensembl:ENSG00000171246 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80467927..80468010 26863196 MeRIP-seq:(Medium) rs933965278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502214,Human_RBP_ID_1370128,Human_RBP_ID_8823251,Human_RBP_ID_17902466,Human_RBP_ID_22500671,Human_RBP_ID_23753442,Human_RBP_ID_27670005 RMVar_hsa_circ_118545,RMVar_hsa_circ_187520 100755 RMVar_ID_100755 Human_SNP_ID_634284804 m1A Human chr17 + 80468040 80468040 80468040 CTCAACAGTGCTTTTTATCTTCTTGTTTTATAAAATGGCTTACCTGAGAGAGGCATGTATTATTC CTCAACAGTGCTTTTTATCTTCTTGTTTTATACAATGGCTTACCTGAGAGAGGCATGTATTATTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80467989..80468147 26863196 MeRIP-seq:(Medium) rs375713172 Functional Loss SNV dbSNP153 33..33 33 - - - 100756 RMVar_ID_100756 Human_SNP_ID_634284826 m1A Human chr17 + 80468148 80468148 80468148 CTACGTGGATTAGATTTGCGGCTGTGTCATCGACCTTTCTCGGGGCCAGCAAAGTGCCAAGTGTC CTACGTGGATTAGATTTGCGGCTGTGTCATCGCCCTTTCTCGGGGCCAGCAAAGTGCCAAGTGTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:80468056..80468275 26863196 MeRIP-seq:(Medium) rs1225165938 Functional Loss SNV dbSNP153 33..33 33 - - - 100757 RMVar_ID_100757 Human_SNP_ID_634284851 m1A Human chr17 - 80468266 80468266 80468266 CTCACCTTCCTCACCCCTCCTCTGACCCACCCATGGTGCCAGGGCCGAAGCTGACCTTTAGCTCC CTCACCTTCCTCACCCCTCCTCTGACCCACCCGTGGTGCCAGGGCCGAAGCTGACCTTTAGCTCC T C NPTX1 Ensembl:ENSG00000171246 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:80468167..80468309 26863196 MeRIP-seq:(Medium) rs1033893556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502220,Human_RBP_ID_4457524,Human_RBP_ID_22422012,Human_RBP_ID_27458461 RMVar_hsa_circ_118545,RMVar_hsa_circ_187520 100758 RMVar_ID_100758 Human_SNP_ID_634284991 m1A Human chr17 + 80468784 80468784 80468784 GGTCACAGAACACTGGGCGGCACTCGGCACACAACACAGAACCGGGGCAGTCCATGCAGGTGCGG GGTCACAGAACACTGGGCGGCACTCGGCACACGACACAGAACCGGGGCAGTCCATGCAGGTGCGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80468776..80468800 26863196 MeRIP-seq:(Medium) rs1017844757 Functional Loss SNV dbSNP153 33..33 33 - - - 100759 RMVar_ID_100759 Human_SNP_ID_634285040 m1A Human chr17 - 80468953 80468953 80468953 AGATCAGGCGCCGTGCTGCGCGTTGTTGTTCAACAGTGGCTTTTTCTTAGATAATCGTGCTTCCT AGATCAGGCGCCGTGCTGCGCGTTGTTGTTCACCAGTGGCTTTTTCTTAGATAATCGTGCTTCCT T G NPTX1 Ensembl:ENSG00000171246 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80468902..80468985 26863196 MeRIP-seq:(Medium) rs1017518254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502243,Human_RBP_ID_3539012,Human_RBP_ID_18179208,Human_RBP_ID_18296945,Human_RBP_ID_23753453 Human_miRNA_ID_1315383,Human_miRNA_ID_2977758 RMVar_hsa_circ_118545,RMVar_hsa_circ_187520 100760 RMVar_ID_100760 Human_SNP_ID_634286989 m1A Human chr17 + 80475612 80475612 80475612 TGTCGTTCCTGGGGCCCCCCTTGCCCTCCTCCAGGGTGTTCACCCGGGACAGCACCTGCCTCTCC TGTCGTTCCTGGGGCCCCCCTTGCCCTCCTCCGGGGTGTTCACCCGGGACAGCACCTGCCTCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80475562..80475665 26863196 MeRIP-seq:(Medium) rs202053640 Functional Loss SNV dbSNP153 33..33 33 - - - 100761 RMVar_ID_100761 Human_SNP_ID_634287243 m1A Human chr17 - 80476220 80476220 80476220 GCTGCAGCAGAAGGAGACCATCCTGAGCCAGAAGGAGACCATCCGCGAGCTGACCGCCAAGCTGG GCTGCAGCAGAAGGAGACCATCCTGAGCCAGAGGGAGACCATCCGCGAGCTGACCGCCAAGCTGG T C NPTX1 Ensembl:ENSG00000171246 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80476201..80476250 26863196 MeRIP-seq:(Medium) rs1340280697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134025,Human_RBP_ID_5577969 100762 RMVar_ID_100762 Human_SNP_ID_634287372 m1A Human chr17 - 80476563 80476563 80476563 CTGATAGCGCGGCGGTGTGGACCGCGCGGCCGAAGAGCGCGGCGCCCAGAGCGCGGGCCGCTCGC CTGATAGCGCGGCGGTGTGGACCGCGCGGCCGGAGAGCGCGGCGCCCAGAGCGCGGGCCGCTCGC T C NPTX1 Ensembl:ENSG00000171246 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80475995..80476600 26863196 MeRIP-seq:(Medium) rs868703874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4457708 100763 RMVar_ID_100763 Human_SNP_ID_634289080 m1A Human chr17 - 80482752 80482752 80482752 TTGCTAGTGCCAGCCCCCTTGGCTCACTCTTCAAGCCCCTGTTATCACCTCCACAGGAGACCCTT TTGCTAGTGCCAGCCCCCTTGGCTCACTCTTCGAGCCCCTGTTATCACCTCCACAGGAGACCCTT T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80482702..80482778 26863196 MeRIP-seq:(Medium) rs1375153235 Functional Loss SNV dbSNP153 33..33 33 - - - 100764 RMVar_ID_100764 Human_SNP_ID_634291249 m1A Human chr17 + 80490051 80490015 80490052 AGAGGAATGGATGTGGTGGAGGGGAGGAACGCATTGGAGAAGATGGACACAGTGGAGGGGAGGGA __________________________________TGGAGAAGATGGACACAGTGGAGGGGAGGGA GTGGAGAGGAATGGATGTGGTGGAGGGGAGGAACGCAT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80490001..80490066 26863196 MeRIP-seq:(Medium) rs1568280160 Functional Loss DEL dbSNP153 1..34 33 - - - 100765 RMVar_ID_100765 Human_SNP_ID_634291271 m1A Human chr17 + 80490051 80490051 80490051 AGAGGAATGGATGTGGTGGAGGGGAGGAACGCATTGGAGAAGATGGACACAGTGGAGGGGAGGGA AGAGGAATGGATGTGGTGGAGGGGAGGAACGCGTTGGAGAAGATGGACACAGTGGAGGGGAGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80490001..80490066 26863196 MeRIP-seq:(Medium) rs1189524903 Functional Loss SNV dbSNP153 33..33 33 - - - 100766 RMVar_ID_100766 Human_SNP_ID_634291302 m1A Human chr17 - 80490127 80490127 80490127 ATCCATCCCTGTCCACCACGCTCATCTTCTCCACCACGTCCATCCCTCTCTAATGCATCCGTCTC ATCCATCCCTGTCCACCACGCTCATCTTCTCCGCCACGTCCATCCCTCTCTAATGCATCCGTCTC T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80490018..80490151 26863196 MeRIP-seq:(Medium) rs971830829 Functional Loss SNV dbSNP153 33..33 33 - - - 100767 RMVar_ID_100767 Human_SNP_ID_634291303 m1A Human chr17 - 80490127 80490127 80490127 ATCCATCCCTGTCCACCACGCTCATCTTCTCCACCACGTCCATCCCTCTCTAATGCATCCGTCTC ATCCATCCCTGTCCACCACGCTCATCTTCTCCCCCACGTCCATCCCTCTCTAATGCATCCGTCTC T G lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80490018..80490151 26863196 MeRIP-seq:(Medium) rs971830829 Functional Loss SNV dbSNP153 33..33 33 - - - 100768 RMVar_ID_100768 Human_SNP_ID_634292019 m1A Human chr17 + 80492465 80492465 80492465 GGGCAGGTGGTGCAGGTGGTGGTGCAGGTGGCAGGGCAGGTGGCGGTGCAGGTGGCGGGGCAGGT GGGCAGGTGGTGCAGGTGGTGGTGCAGGTGGCGGGGCAGGTGGCGGTGCAGGTGGCGGGGCAGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80492299..80492573 26863196 MeRIP-seq:(Medium) rs1228074353 Functional Loss SNV dbSNP153 33..33 33 - - - 100769 RMVar_ID_100769 Human_SNP_ID_634294991 m1A Human chr17 + 80503310 80503310 80503310 GTGGATGGAGGGATGGGTGGATAGATGGAGGGATGGAGGGGTGGATGAATAGTGTGTATGGATAA GTGGATGGAGGGATGGGTGGATAGATGGAGGGGTGGAGGGGTGGATGAATAGTGTGTATGGATAA A G HSALNG0119202 RNACentral:URS0000E969EB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80503266..80503382 26863196 MeRIP-seq:(Medium) rs950058385 Functional Loss SNV dbSNP153 33..33 33 - - - 100770 RMVar_ID_100770 Human_SNP_ID_634295168 m1A Human chr17 + 80503837 80503837 80503837 ATAAGTGGATGGAGGGATGGGTAGATGGGTGGATGTGTGGATGGAGGATGGTGGATAGGTAGACG ATAAGTGGATGGAGGGATGGGTAGATGGGTGGGTGTGTGGATGGAGGATGGTGGATAGGTAGACG A G HSALNG0119202 RNACentral:URS0000E969EB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80503813..80503945 26863196 MeRIP-seq:(Medium) rs1355114159 Functional Loss SNV dbSNP153 33..33 33 - - - 100771 RMVar_ID_100771 Human_SNP_ID_634295313 m1A Human chr17 - 80504309 80504309 80504309 ACCCATCCCTTCATTCACCCTACCATCAATACATTCACCCATCCCTCCATCCACCCATCTACCCC ACCCATCCCTTCATTCACCCTACCATCAATACCTTCACCCATCCCTCCATCCACCCATCTACCCC T G lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80504261..80504465 26863196 MeRIP-seq:(Medium) rs1451754210 Functional Loss SNV dbSNP153 33..33 33 - - - 100772 RMVar_ID_100772 Human_SNP_ID_634306048 m1A Human chr17 + 80545022 80545022 80545022 GGCAGGAGAGAGCCTCGGGGCTGAAGGCCAGGACCAGCCAGGCCGCGCGGACCTGAGGTTGAGGA GGCAGGAGAGAGCCTCGGGGCTGAAGGCCAGGCCCAGCCAGGCCGCGCGGACCTGAGGTTGAGGA A C RPTOR Ensembl:ENSG00000141564 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:80544876..80545175 26863196 MeRIP-seq:(Medium) rs1568295947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526042,Human_RBP_ID_13188644,Human_RBP_ID_22062903,Human_RBP_ID_26332528 RMVar_hsa_circ_85423,RMVar_hsa_circ_115028,RMVar_hsa_circ_187521,RMVar_hsa_circ_187522 100773 RMVar_ID_100773 Human_SNP_ID_634318534 m1A Human chr17 + 80594985 80594985 80594985 AGTAACTGCCTGGGCTGATGTGTGTGCCTGAGAGTCAGAGAGAGAGAGGGAGAAAGAGAATGGGG AGTAACTGCCTGGGCTGATGTGTGTGCCTGAGGGTCAGAGAGAGAGAGGGAGAAAGAGAATGGGG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80594974..80595044 26863196 MeRIP-seq:(Medium) rs1235138769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13242606 RMVar_hsa_circ_85423,RMVar_hsa_circ_115028,RMVar_hsa_circ_187521,RMVar_hsa_circ_187522 100774 RMVar_ID_100774 Human_SNP_ID_634319014 m1A Human chr17 - 80597215 80597215 80597215 CAAGTCCCAGCTCAAGTTCCATCCCCTCTACGAGGCTCTCCCAACCATTCTGCACCTCTCCTACT CAAGTCCCAGCTCAAGTTCCATCCCCTCTACGTGGCTCTCCCAACCATTCTGCACCTCTCCTACT T A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80597205..80597279 26863196 MeRIP-seq:(Medium) rs954991782 Functional Loss SNV dbSNP153 33..33 33 - - - 100775 RMVar_ID_100775 Human_SNP_ID_634330277 m1A Human chr17 + 80639768 80639768 80639768 GAGAGTCTCAGTAGCATCGTGAAGGGCTGCGGATTGGGTGAACATGTTAGCAGTGGCTGGTGGAG GAGAGTCTCAGTAGCATCGTGAAGGGCTGCGGGTTGGGTGAACATGTTAGCAGTGGCTGGTGGAG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80639763..80639836 26863196 MeRIP-seq:(Medium) rs1475106412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36197,RMVar_hsa_circ_85423,RMVar_hsa_circ_115028,RMVar_hsa_circ_127509,RMVar_hsa_circ_187521,RMVar_hsa_circ_187522,RMVar_hsa_circ_313621,RMVar_hsa_circ_335444,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_187525 100776 RMVar_ID_100776 Human_SNP_ID_634337198 m1A Human chr17 + 80667228 80667228 80667228 GAAGTAAGTCCATACCACATTGGAAGAGTTAGACGGGTCTTGGAGAGGCTGGAGGGGGACAGCCG GAAGTAAGTCCATACCACATTGGAAGAGTTAGGCGGGTCTTGGAGAGGCTGGAGGGGGACAGCCG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80667218..80667347 26863196 MeRIP-seq:(Medium) rs1305923844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25329959 RMVar_hsa_circ_84972,RMVar_hsa_circ_36197,RMVar_hsa_circ_85423,RMVar_hsa_circ_127509,RMVar_hsa_circ_187522,RMVar_hsa_circ_313621,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_187527 100777 RMVar_ID_100777 Human_SNP_ID_634337212 m1A Human chr17 + 80667272 80667272 80667272 GAGGCTGGAGGGGGACAGCCGGGGGAAGCTCCATAGAGGTGGTGACGTCTGAGCTGGGAGCGAAG GAGGCTGGAGGGGGACAGCCGGGGGAAGCTCCGTAGAGGTGGTGACGTCTGAGCTGGGAGCGAAG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80667226..80667318 26863196 MeRIP-seq:(Medium) rs921846965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84972,RMVar_hsa_circ_36197,RMVar_hsa_circ_85423,RMVar_hsa_circ_127509,RMVar_hsa_circ_187522,RMVar_hsa_circ_313621,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_187527 100778 RMVar_ID_100778 Human_SNP_ID_634356746 m1A Human chr17 - 80741790 80741790 80741790 CGACTGGCCTCTCCTCTCCAGCCACACGAACCACATGGGGGCTCGTCACCATCCCGTGGCTTCAG CGACTGGCCTCTCCTCTCCAGCCACACGAACCTCATGGGGGCTCGTCACCATCCCGTGGCTTCAG T A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80741783..80741990 26863196 MeRIP-seq:(Medium) rs767466617 Functional Loss SNV dbSNP153 33..33 33 - - - 100779 RMVar_ID_100779 Human_SNP_ID_634359512 m1A Human chr17 - 80748135 80748132 80748136 ACAGGTCCTCACGCCACGGCCTCTAAACACACACCGCAGTCCCTCCATCCACCCAACAGGTCCTC ACAGGTCCTCACGCCACGGCCTCTAAACACA____GCAGTCCCTCCATCCACCCAACAGGTCCTC CGGTG C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80748105..80748204 26863196 MeRIP-seq:(Medium) rs1385799214 Functional Loss DEL dbSNP153 32..35 33 - - - 100780 RMVar_ID_100780 Human_SNP_ID_634359524 m1A Human chr17 - 80748157 80748157 80748157 CCGCAGCCCCTCCATCCACCCAACAGGTCCTCACGCCACGGCCTCTAAACACACACCGCAGTCCC CCGCAGCCCCTCCATCCACCCAACAGGTCCTCTCGCCACGGCCTCTAAACACACACCGCAGTCCC T A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80748104..80748212 26863196 MeRIP-seq:(Medium) rs2440664 Functional Loss SNV dbSNP153 33..33 33 - - - 100781 RMVar_ID_100781 Human_SNP_ID_634359525 m1A Human chr17 - 80748157 80748157 80748157 CCGCAGCCCCTCCATCCACCCAACAGGTCCTCACGCCACGGCCTCTAAACACACACCGCAGTCCC CCGCAGCCCCTCCATCCACCCAACAGGTCCTCCCGCCACGGCCTCTAAACACACACCGCAGTCCC T G lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80748104..80748212 26863196 MeRIP-seq:(Medium) rs2440664 Functional Loss SNV dbSNP153 33..33 33 - - - 100782 RMVar_ID_100782 Human_SNP_ID_634359526 m1A Human chr17 + 80748162 80748162 80748162 TGCGGTGTGTGTTTAGAGGCCGTGGCGTGAGGACCTGTTGGGTGGATGGAGGGGCTGCGGTGTGT TGCGGTGTGTGTTTAGAGGCCGTGGCGTGAGGGCCTGTTGGGTGGATGGAGGGGCTGCGGTGTGT A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80748112..80748195 26863196 MeRIP-seq:(Medium) rs2589147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190346 RMVar_hsa_circ_127509,RMVar_hsa_circ_313621,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_355401,RMVar_hsa_circ_331869,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_334118,RMVar_hsa_circ_332466,RMVar_hsa_circ_187536,RMVar_hsa_circ_102436,RMVar_hsa_circ_187537,RMVar_hsa_circ_187535 100783 RMVar_ID_100783 Human_SNP_ID_634359833 m1A Human chr17 + 80749240 80749240 80749240 AGGGACTGCGGTGTGAGTTTAGAGGCCGTGGCAGGAGGACCTGTTGGGTGGATGGAGGGGCTGCG AGGGACTGCGGTGTGAGTTTAGAGGCCGTGGCGGGAGGACCTGTTGGGTGGATGGAGGGGCTGCG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80749238..80749432 26863196 MeRIP-seq:(Medium) rs868339341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127509,RMVar_hsa_circ_313621,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_355401,RMVar_hsa_circ_331869,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_334118,RMVar_hsa_circ_332466,RMVar_hsa_circ_187536,RMVar_hsa_circ_102436,RMVar_hsa_circ_187537,RMVar_hsa_circ_187535 100784 RMVar_ID_100784 Human_SNP_ID_634377364 m1A Human chr17 + 80816583 80816583 80816583 GAGCAGATCCTGGGGTGTGAAAAGAGCTGGCGACGCAGTGCTCCCAGAGGTCACTAAGGGAGGAG GAGCAGATCCTGGGGTGTGAAAAGAGCTGGCGCCGCAGTGCTCCCAGAGGTCACTAAGGGAGGAG A C RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80816581..80816780 26863196 MeRIP-seq:(Medium) rs1013524898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_102436,RMVar_hsa_circ_187537,RMVar_hsa_circ_10994,RMVar_hsa_circ_52486 100785 RMVar_ID_100785 Human_SNP_ID_634384306 m1A Human chr17 - 80840418 80840408 80840418 AGTGAGCTGCCGTGTGGTGAGAGTGAGCTGCCATGCGGTGAATGTGAGCTGCCATGCAGTGAGAG AGTGAGCTGCCGTGTGGTGAGAGTGAGCTGCCGTGTGGTGAGAGTGAGCTGCCATGCAGTGAGAG ATTCACCGCAT TCTCACCACAC lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80840416..80840542 26863196 MeRIP-seq:(Medium) rs71356671 Functional Loss MNV dbSNP153 33..43 33 - - - 100786 RMVar_ID_100786 Human_SNP_ID_634384312 m1A Human chr17 - 80840418 80840418 80840418 AGTGAGCTGCCGTGTGGTGAGAGTGAGCTGCCATGCGGTGAATGTGAGCTGCCATGCAGTGAGAG AGTGAGCTGCCGTGTGGTGAGAGTGAGCTGCCGTGCGGTGAATGTGAGCTGCCATGCAGTGAGAG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80840416..80840542 26863196 MeRIP-seq:(Medium) rs1429648647 Functional Loss SNV dbSNP153 33..33 33 - - - 100787 RMVar_ID_100787 Human_SNP_ID_634384635 m1A Human chr17 - 80840833 80840829 80840833 GCCGTGTGGTGAGTGTGAGCTGCCGTGCGGTGAGTGTGAGCTGCGGCGTGGTGAGAGTGAGCTGC GCCGTGTGGTGAGTGTGAGCTGCCGTGCGGTG____TGAGCTGCGGCGTGGTGAGAGTGAGCTGC ACACT A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80840786..80840877 26863196 MeRIP-seq:(Medium) rs1226612195 Functional Loss DEL dbSNP153 33..36 33 - - - 100788 RMVar_ID_100788 Human_SNP_ID_634384636 m1A Human chr17 - 80840833 80840831 80840833 GCCGTGTGGTGAGTGTGAGCTGCCGTGCGGTGAGTGTGAGCTGCGGCGTGGTGAGAGTGAGCTGC GCCGTGTGGTGAGTGTGAGCTGCCGTGCGGTG__TGTGAGCTGCGGCGTGGTGAGAGTGAGCTGC ACT A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80840786..80840877 26863196 MeRIP-seq:(Medium) rs1454762413 Functional Loss DEL dbSNP153 33..34 33 - - - 100789 RMVar_ID_100789 Human_SNP_ID_634384651 m1A Human chr17 + 80840852 80840852 80840852 CCGCAGCTCACACTCACCGCACGGCAGCTCACACTCACCACACGGCAGCTCACTCTCACCACACG CCGCAGCTCACACTCACCGCACGGCAGCTCACCCTCACCACACGGCAGCTCACTCTCACCACACG A C RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80840718..80840875 26863196 MeRIP-seq:(Medium) rs1431176632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59,RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_10994,RMVar_hsa_circ_344276,RMVar_hsa_circ_33259,RMVar_hsa_circ_7214,RMVar_hsa_circ_187538,RMVar_hsa_circ_86459,RMVar_hsa_circ_292318,RMVar_hsa_circ_373270,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_187540 100790 RMVar_ID_100790 Human_SNP_ID_634384652 m1A Human chr17 + 80840852 80840852 80840852 CCGCAGCTCACACTCACCGCACGGCAGCTCACACTCACCACACGGCAGCTCACTCTCACCACACG CCGCAGCTCACACTCACCGCACGGCAGCTCACTCTCACCACACGGCAGCTCACTCTCACCACACG A T RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80840718..80840875 26863196 MeRIP-seq:(Medium) rs1431176632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59,RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_10994,RMVar_hsa_circ_344276,RMVar_hsa_circ_33259,RMVar_hsa_circ_7214,RMVar_hsa_circ_187538,RMVar_hsa_circ_86459,RMVar_hsa_circ_292318,RMVar_hsa_circ_373270,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_187540 100791 RMVar_ID_100791 Human_SNP_ID_634385115 m1A Human chr17 + 80841556 80841556 80841556 AGCTCACTCTCACCACACGGCAGCTCACTCTCACCGCACGGCAGATCACTCTCACCGCACGGCAG AGCTCACTCTCACCACACGGCAGCTCACTCTCGCCGCACGGCAGATCACTCTCACCGCACGGCAG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80841549..80841793 26863196 MeRIP-seq:(Medium) rs1228972442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59,RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_10994,RMVar_hsa_circ_344276,RMVar_hsa_circ_33259,RMVar_hsa_circ_7214,RMVar_hsa_circ_187538,RMVar_hsa_circ_86459,RMVar_hsa_circ_292318,RMVar_hsa_circ_373270,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_187540 100792 RMVar_ID_100792 Human_SNP_ID_634385377 m1A Human chr17 + 80841949 80841949 80841949 CGGCAGCTCACACTCACCGCACGGCAGCTCACACTCACCGCACGGCAGCTCACTCTCACCGCACC CGGCAGCTCACACTCACCGCACGGCAGCTCACTCTCACCGCACGGCAGCTCACTCTCACCGCACC A T RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80841948..80842046 26863196 MeRIP-seq:(Medium) rs373983036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59,RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_10994,RMVar_hsa_circ_344276,RMVar_hsa_circ_33259,RMVar_hsa_circ_7214,RMVar_hsa_circ_187538,RMVar_hsa_circ_86459,RMVar_hsa_circ_292318,RMVar_hsa_circ_373270,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_187540 100793 RMVar_ID_100793 Human_SNP_ID_634390022 m1A Human chr17 - 80858674 80858674 80858674 CAAGGCCCTTCCTGGCGTTTCCAGTTCAGCATAGGCCGGGTCTCGCCCACACGACTTCTCAGCCC CAAGGCCCTTCCTGGCGTTTCCAGTTCAGCATGGGCCGGGTCTCGCCCACACGACTTCTCAGCCC T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80858670..80858816 26863196 MeRIP-seq:(Medium) rs1031361744 Functional Loss SNV dbSNP153 33..33 33 - - - 100794 RMVar_ID_100794 Human_SNP_ID_634400029 m1A Human chr17 - 80893302 80893298 80893302 ACCTGGCGCGCGCACACACCTGGCGCACACACACACCCGGCGCACACACACCCTGGTACACACGC ACCTGGCGCGCGCACACACCTGGCGCACACAC____CCGGCGCACACACACCCTGGTACACACGC GGTGT G lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80893278..80893384 32194978 MeRIP-seq:(Medium) rs1032401267 Functional Loss DEL dbSNP153 33..36 33 - - - 100795 RMVar_ID_100795 Human_SNP_ID_634400030 m1A Human chr17 - 80893302 80893298 80893302 ACCTGGCGCGCGCACACACCTGGCGCACACACACACCCGGCGCACACACACCCTGGTACACACGC ACCTGGCGCGCGCACACACCTGGCGCACACAC__ACCCGGCGCACACACACCCTGGTACACACGC GGTGT GGT lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80893278..80893384 32194978 MeRIP-seq:(Medium) rs1032401267 Functional Loss DEL dbSNP153 33..34 33 - - - 100796 RMVar_ID_100796 Human_SNP_ID_634401242 m1A Human chr17 + 80896492 80896491 80896493 CGGCCGCACCGACACATCCCACGGCCGCACCGACACACCCCACGGCCGCACCGACACCCCGCATA CGGCCGCACCGACACATCCCACGGCCGCACCG__ACACCCCACGGCCGCACCGACACCCCGCATA GAC G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80896490..80896576 26863196 MeRIP-seq:(Medium) rs1172583367 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_187555,RMVar_hsa_circ_44577,RMVar_hsa_circ_22,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_105746,RMVar_hsa_circ_83561,RMVar_hsa_circ_106757,RMVar_hsa_circ_333783,RMVar_hsa_circ_187545,RMVar_hsa_circ_187546,RMVar_hsa_circ_377355,RMVar_hsa_circ_367873,RMVar_hsa_circ_33775,RMVar_hsa_circ_108926,RMVar_hsa_circ_187547,RMVar_hsa_circ_187548,RMVar_hsa_circ_187550,RMVar_hsa_circ_83314,RMVar_hsa_circ_187549,RMVar_hsa_circ_112636,RMVar_hsa_circ_93903,RMVar_hsa_circ_123403,RMVar_hsa_circ_372824,RMVar_hsa_circ_187551,RMVar_hsa_circ_374025,RMVar_hsa_circ_115513,RMVar_hsa_circ_116660,RMVar_hsa_circ_113923,RMVar_hsa_circ_187559,RMVar_hsa_circ_77699,RMVar_hsa_circ_82169,RMVar_hsa_circ_187560,RMVar_hsa_circ_187557,RMVar_hsa_circ_187558,RMVar_hsa_circ_187556,RMVar_hsa_circ_3166,RMVar_hsa_circ_187553,RMVar_hsa_circ_187554,RMVar_hsa_circ_187552 100797 RMVar_ID_100797 Human_SNP_ID_634410974 m1A Human chr17 + 80930259 80930259 80930259 TCCCCAGCTCATCCTCAGCTCAGCTCATCCCCAGCTCATCCTCAGCTCATCCCCTGCTCATCCTT TCCCCAGCTCATCCTCAGCTCAGCTCATCCCCTGCTCATCCTCAGCTCATCCCCTGCTCATCCTT A T RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80930111..80930495 26863196 MeRIP-seq:(Medium) rs1159496760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129307,Human_RBP_ID_18942390 RMVar_hsa_circ_187555,RMVar_hsa_circ_105746,RMVar_hsa_circ_83561,RMVar_hsa_circ_106757,RMVar_hsa_circ_187545,RMVar_hsa_circ_187546,RMVar_hsa_circ_367873,RMVar_hsa_circ_33775,RMVar_hsa_circ_108926,RMVar_hsa_circ_187548,RMVar_hsa_circ_187550,RMVar_hsa_circ_83314,RMVar_hsa_circ_187549,RMVar_hsa_circ_112636,RMVar_hsa_circ_93903,RMVar_hsa_circ_123403,RMVar_hsa_circ_187551,RMVar_hsa_circ_374025,RMVar_hsa_circ_116660,RMVar_hsa_circ_113923,RMVar_hsa_circ_77699,RMVar_hsa_circ_187557,RMVar_hsa_circ_187556,RMVar_hsa_circ_3166,RMVar_hsa_circ_187553,RMVar_hsa_circ_187554,RMVar_hsa_circ_187552,RMVar_hsa_circ_2980,RMVar_hsa_circ_187564,RMVar_hsa_circ_187566,RMVar_hsa_circ_324160,RMVar_hsa_circ_329424 100798 RMVar_ID_100798 Human_SNP_ID_634411090 m1A Human chr17 - 80930366 80930366 80930366 AGAATGAGCTGAGCTGAGCTGGGGATGAGCTGAGGATGAGCTGGGGATGAGCTGAGGATGAGCTG AGAATGAGCTGAGCTGAGCTGGGGATGAGCTGGGGATGAGCTGGGGATGAGCTGAGGATGAGCTG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80930353..80930493 26863196 MeRIP-seq:(Medium) rs371225406 Functional Loss SNV dbSNP153 33..33 33 - - - 100799 RMVar_ID_100799 Human_SNP_ID_634413727 m1A Human chr17 + 80940533 80940533 80940533 AGAAGAGCACGACCTGGAGAGTCAGATCCGCAAGGAGCGGGAGTGGCGGTTCCTGCGAAACAGCC AGAAGAGCACGACCTGGAGAGTCAGATCCGCAGGGAGCGGGAGTGGCGGTTCCTGCGAAACAGCC A G RPTOR Ensembl:ENSG00000141564 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80940497..80940568 26863196 MeRIP-seq:(Medium) rs1228855496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18992704 Human_Splice_Rec_1879326,Human_Splice_Rec_1879327,Human_Splice_Rec_1879410,Human_Splice_Rec_1879411,Human_Splice_Rec_1879474,Human_Splice_Rec_1879475 RMVar_hsa_circ_187555,RMVar_hsa_circ_105746,RMVar_hsa_circ_83561,RMVar_hsa_circ_106757,RMVar_hsa_circ_187545,RMVar_hsa_circ_187546,RMVar_hsa_circ_367873,RMVar_hsa_circ_33775,RMVar_hsa_circ_108926,RMVar_hsa_circ_187548,RMVar_hsa_circ_187550,RMVar_hsa_circ_83314,RMVar_hsa_circ_187549,RMVar_hsa_circ_112636,RMVar_hsa_circ_93903,RMVar_hsa_circ_123403,RMVar_hsa_circ_187551,RMVar_hsa_circ_374025,RMVar_hsa_circ_116660,RMVar_hsa_circ_113923,RMVar_hsa_circ_77699,RMVar_hsa_circ_187557,RMVar_hsa_circ_187556,RMVar_hsa_circ_3166,RMVar_hsa_circ_187553,RMVar_hsa_circ_187554,RMVar_hsa_circ_187552,RMVar_hsa_circ_2980,RMVar_hsa_circ_187564,RMVar_hsa_circ_187566,RMVar_hsa_circ_324160,RMVar_hsa_circ_329424,RMVar_hsa_circ_325654 100800 RMVar_ID_100800 Human_SNP_ID_634421550 m1A Human chr17 - 80965562 80965562 80965562 ATGAAGCCACCTGGCTCCTTCACCTCTCAATAATCCTGATTCCCGACGAACACGGAAAGAACACT ATGAAGCCACCTGGCTCCTTCACCTCTCAATAGTCCTGATTCCCGACGAACACGGAAAGAACACT T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80965432..80965995 26863196 MeRIP-seq:(Medium) rs1272246687 Functional Loss SNV dbSNP153 33..33 33 - - - 100801 RMVar_ID_100801 Human_SNP_ID_634421661 m1A Human chr17 - 80965879 80965879 80965879 ACCCGGGCTGCTTTCTCGGCCCAGACGTGGGGATGGGATTCGTGCCGGAACCTTCTTCTGGTGGG ACCCGGGCTGCTTTCTCGGCCCAGACGTGGGGGTGGGATTCGTGCCGGAACCTTCTTCTGGTGGG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:80965685..80966006 26863196 MeRIP-seq:(Medium) rs1396998098 Functional Loss SNV dbSNP153 33..33 33 - - - 100802 RMVar_ID_100802 Human_SNP_ID_634426176 m1A Human chr17 + 80980742 80980739 80980743 GATGAATGAATGAATGAGTGAAGGAGTGGGTGACTGAGTGAATGAGTGAGGGAGTGGGTGAGTGA GATGAATGAATGAATGAGTGAAGGAGTGGG____TGAGTGAATGAGTGAGGGAGTGGGTGAGTGA GTGAC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80980596..80981094 26863196 MeRIP-seq:(Medium) rs1042462264 Functional Loss DEL dbSNP153 31..34 33 - - - 100803 RMVar_ID_100803 Human_SNP_ID_634429429 m1A Human chr17 - 80991929 80991929 80991929 CCGTGACGCGGCTCTGCTTCTTGCGGCCGAACAGGTTACCCATGGCGGCGCCCGCCCCTGGCCCG CCGTGACGCGGCTCTGCTTCTTGCGGCCGAACTGGTTACCCATGGCGGCGCCCGCCCCTGGCCCG T A lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:80991879..80992027 26863196 MeRIP-seq:(Medium) rs1168062579 Functional Loss SNV dbSNP153 33..33 33 - - - 100804 RMVar_ID_100804 Human_SNP_ID_634432255 m1A Human chr17 - 80999680 80999680 80999680 ACTGGAGGTGGGTGTCTAGGGTGCGGAGGCAGAGGCACAGAGAGGTTCAGCACATGCTGGTCTCC ACTGGAGGTGGGTGTCTAGGGTGCGGAGGCAGGGGCACAGAGAGGTTCAGCACATGCTGGTCTCC T C AC127496.6 Ensembl:ENSG00000263218 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80999629..80999743 26863196 MeRIP-seq:(Medium) rs551348333 Functional Loss SNV dbSNP153 33..33 33 - - - 100805 RMVar_ID_100805 Human_SNP_ID_634432331 m1A Human chr17 + 80999916 80999916 80999916 GGGTCCCCGCGGCTGGGGCTCATGGAACTGCGAGACCCGGGACCCTCCTGCCCTGCGGGTCCCCG GGGTCCCCGCGGCTGGGGCTCATGGAACTGCGGGACCCGGGACCCTCCTGCCCTGCGGGTCCCCG A G CHMP6 Ensembl:ENSG00000176108 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80999870..81000088 26863196 MeRIP-seq:(Medium) rs59126871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464871,Human_RBP_ID_13193493,Human_RBP_ID_27261555 RMVar_hsa_circ_84385,RMVar_hsa_circ_187567,RMVar_hsa_circ_88358,RMVar_hsa_circ_121725,RMVar_hsa_circ_187570,RMVar_hsa_circ_187571 100806 RMVar_ID_100806 Human_SNP_ID_634432954 m1A Human chr17 - 81001604 81001604 81001604 TCCACTCTGAGCCACCCTTTGTGTGGCCCCCTACTCTGTGTCCCTGCCCTCTGCAGCCTCTCCTC TCCACTCTGAGCCACCCTTTGTGTGGCCCCCTGCTCTGTGTCCCTGCCCTCTGCAGCCTCTCCTC T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81001555..81001632 26863196 MeRIP-seq:(Medium) rs114105377 Functional Loss SNV dbSNP153 33..33 33 - - - 100807 RMVar_ID_100807 Human_SNP_ID_634441831 m1A Human chr17 - 81031598 81031598 81031598 GGAGTTTTGCTAAACAGAAGGAGCCCTTTCTGAGGTGACCACCCGTCAAAACTTGAACCCGCTTC GGAGTTTTGCTAAACAGAAGGAGCCCTTTCTGCGGTGACCACCCGTCAAAACTTGAACCCGCTTC T G BAIAP2-DT Ensembl:ENSG00000226137 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81031562..81031677 26863196 MeRIP-seq:(Medium) rs1299081022 Functional Loss SNV dbSNP153 33..33 33 - - - 100808 RMVar_ID_100808 Human_SNP_ID_634441933 m1A Human chr17 + 81031884 81031884 81031884 CCGGCTGTGGCGTCGGGTTCCTGTCTGAAGTCACTCTTGCCTCCGGCCCCGCTCGGCGCCCTGTG CCGGCTGTGGCGTCGGGTTCCTGTCTGAAGTCCCTCTTGCCTCCGGCCCCGCTCGGCGCCCTGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81031834..81031949 32194978 MeRIP-seq:(Medium) rs998113225 Functional Loss SNV dbSNP153 33..33 33 - - - 100809 RMVar_ID_100809 Human_SNP_ID_634441934 m1A Human chr17 + 81031884 81031884 81031884 CCGGCTGTGGCGTCGGGTTCCTGTCTGAAGTCACTCTTGCCTCCGGCCCCGCTCGGCGCCCTGTG CCGGCTGTGGCGTCGGGTTCCTGTCTGAAGTCGCTCTTGCCTCCGGCCCCGCTCGGCGCCCTGTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81031834..81031949 32194978 MeRIP-seq:(Medium) rs998113225 Functional Loss SNV dbSNP153 33..33 33 - - - 100810 RMVar_ID_100810 Human_SNP_ID_634442483 m1A Human chr17 - 81033269 81033269 81033269 CAGGTGGGGGTAGAGCAGCTCTGCTCGCCTGGAGGAAAGTTGAATGGCTGGAACCAAGATGACAG CAGGTGGGGGTAGAGCAGCTCTGCTCGCCTGGGGGAAAGTTGAATGGCTGGAACCAAGATGACAG T C BAIAP2-DT Ensembl:ENSG00000226137 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81033218..81033333 26863196 MeRIP-seq:(Medium) rs535732442 Functional Loss SNV dbSNP153 33..33 33 - - - 100811 RMVar_ID_100811 Human_SNP_ID_634449965 m1A Human chr17 + 81053621 81053621 81053621 TCTCCTCTGTGTTCGGACCCTTCGGAGTCACCAGGGTGACCTCTGCCAGTAATGCTGTTTCTTCT TCTCCTCTGTGTTCGGACCCTTCGGAGTCACCGGGGTGACCTCTGCCAGTAATGCTGTTTCTTCT A G BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81053617..81053682 26863196 MeRIP-seq:(Medium) rs766267572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92681,RMVar_hsa_circ_187572 100812 RMVar_ID_100812 Human_SNP_ID_634458989 m1A Human chr17 + 81078446 81078446 81078446 TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTATGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTGTGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG A G BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81078056..81078721;chr17:81078107..81078682 26863196 MeRIP-seq:(Medium) rs368379695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12563,RMVar_hsa_circ_267105,RMVar_hsa_circ_290688,RMVar_hsa_circ_23177,RMVar_hsa_circ_187574,RMVar_hsa_circ_63293 100813 RMVar_ID_100813 Human_SNP_ID_634458990 m1A Human chr17 + 81078446 81078446 81078446 TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTATGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTTTGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG A T BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81078056..81078721;chr17:81078107..81078682 26863196 MeRIP-seq:(Medium) rs368379695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12563,RMVar_hsa_circ_267105,RMVar_hsa_circ_290688,RMVar_hsa_circ_23177,RMVar_hsa_circ_187574,RMVar_hsa_circ_63293 100814 RMVar_ID_100814 Human_SNP_ID_634459046 m1A Human chr17 - 81078570 81078570 81078570 CGGCACCCGCACCCACAGCACCCAGCTCGGAGATGGCACCTGCACCCACAGCGCCCGGCTCCCAC CGGCACCCGCACCCACAGCACCCAGCTCGGAGGTGGCACCTGCACCCACAGCGCCCGGCTCCCAC T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:81078469..81078618 26863196 MeRIP-seq:(Medium) rs1232626857 Functional Loss SNV dbSNP153 33..33 33 - - - 100815 RMVar_ID_100815 Human_SNP_ID_634459060 m1A Human chr17 + 81078604 81078604 81078604 TCCGAGCTGGGTGCTGTGGGTGCGGGTGCCGTATTGGGTGGGAGCCGGGCTCTGTGGGTGCAGGT TCCGAGCTGGGTGCTGTGGGTGCGGGTGCCGTCTTGGGTGGGAGCCGGGCTCTGTGGGTGCAGGT A C BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81078599..81078691 26863196 MeRIP-seq:(Medium) rs1282187692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262765,Human_RBP_ID_5319327,Human_RBP_ID_8190380,Human_RBP_ID_26782851 RMVar_hsa_circ_12563,RMVar_hsa_circ_267105,RMVar_hsa_circ_290688,RMVar_hsa_circ_23177,RMVar_hsa_circ_187574,RMVar_hsa_circ_63293 100816 RMVar_ID_100816 Human_SNP_ID_634459061 m1A Human chr17 + 81078604 81078604 81078604 TCCGAGCTGGGTGCTGTGGGTGCGGGTGCCGTATTGGGTGGGAGCCGGGCTCTGTGGGTGCAGGT TCCGAGCTGGGTGCTGTGGGTGCGGGTGCCGTGTTGGGTGGGAGCCGGGCTCTGTGGGTGCAGGT A G BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81078599..81078691 26863196 MeRIP-seq:(Medium) rs1282187692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262765,Human_RBP_ID_5319327,Human_RBP_ID_8190380,Human_RBP_ID_26782851 RMVar_hsa_circ_12563,RMVar_hsa_circ_267105,RMVar_hsa_circ_290688,RMVar_hsa_circ_23177,RMVar_hsa_circ_187574,RMVar_hsa_circ_63293 100817 RMVar_ID_100817 Human_SNP_ID_634461326 m1A Human chr17 - 81085313 81085313 81085313 AGAGGTCGCAGGGCCCATGGGCCTGAACTGACACCAGGGTCAGACCCCTGGCTTTAGACAGGATG AGAGGTCGCAGGGCCCATGGGCCTGAACTGACGCCAGGGTCAGACCCCTGGCTTTAGACAGGATG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81085285..81085389 32194978 MeRIP-seq:(Medium) rs1415531605 Functional Loss SNV dbSNP153 33..33 33 - - - 100818 RMVar_ID_100818 Human_SNP_ID_634468390 m1A Human chr17 + 81104001 81104001 81104001 CTACAGCCCGTGGGCTGACCGCAAGGCTGCCCAGCCCAAATCCCTGTCTCCTCCGCAGTCTCAGA CTACAGCCCGTGGGCTGACCGCAAGGCTGCCCGGCCCAAATCCCTGTCTCCTCCGCAGTCTCAGA A G BAIAP2 Ensembl:ENSG00000175866 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81103951..81104125 26863196 MeRIP-seq:(Medium) rs1310518534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502362 Human_Splice_Rec_1879614,Human_Splice_Rec_1879674,Human_Splice_Rec_1879700,Human_Splice_Rec_1879726,Human_Splice_Rec_1879752,Human_Splice_Rec_1879780,Human_Splice_Rec_1879808,Human_Splice_Rec_1879900,Human_Splice_Rec_1879956,Human_Splice_Rec_1879982,Human_Splice_Rec_1879990 Human_miRNA_ID_1357948 RMVar_hsa_circ_12563,RMVar_hsa_circ_23177,RMVar_hsa_circ_348672,RMVar_hsa_circ_65124,RMVar_hsa_circ_66655,RMVar_hsa_circ_32036 100819 RMVar_ID_100819 Human_SNP_ID_634468400 m1A Human chr17 - 81104017 81104017 81104017 GAGTCGCTGAGCTTGCTCTGAGACTGCGGAGGAGACAGGGATTTGGGCTGGGCAGCCTTGCGGTC GAGTCGCTGAGCTTGCTCTGAGACTGCGGAGGGGACAGGGATTTGGGCTGGGCAGCCTTGCGGTC T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81103967..81104056 26863196 MeRIP-seq:(Medium) rs762128990 Functional Loss SNV dbSNP153 33..33 33 - - - 100820 RMVar_ID_100820 Human_SNP_ID_634468408 m1A Human chr17 + 81104033 81104033 81104033 AGCCCAAATCCCTGTCTCCTCCGCAGTCTCAGAGCAAGCTCAGCGACTCCTACTCCAACACACTC AGCCCAAATCCCTGTCTCCTCCGCAGTCTCAGGGCAAGCTCAGCGACTCCTACTCCAACACACTC A G BAIAP2 Ensembl:ENSG00000175866 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81103982..81104059 26863196 MeRIP-seq:(Medium) rs751497094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1879615,Human_Splice_Rec_1879675,Human_Splice_Rec_1879701,Human_Splice_Rec_1879727,Human_Splice_Rec_1879753,Human_Splice_Rec_1879781,Human_Splice_Rec_1879809,Human_Splice_Rec_1879957,Human_Splice_Rec_1879983,Human_Splice_Rec_1879991,Human_Splice_Rec_1879999 RMVar_hsa_circ_12563,RMVar_hsa_circ_23177,RMVar_hsa_circ_348672,RMVar_hsa_circ_65124,RMVar_hsa_circ_66655,RMVar_hsa_circ_32036 100821 RMVar_ID_100821 Human_SNP_ID_634468610 m1A Human chr17 + 81104478 81104477 81104478 CAGACTCCCTGGGCTTTGCTGCCCCGCCAGCCAGGGGCAGTCCCCTTACCTGTCCCTTGTCCCAG CAGACTCCCTGGGCTTTGCTGCCCCGCCAGCC_GGGGCAGTCCCCTTACCTGTCCCTTGTCCCAG CA C BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81104471..81104580 26863196 MeRIP-seq:(Medium) rs745380364 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22543841 RMVar_hsa_circ_12563,RMVar_hsa_circ_23177,RMVar_hsa_circ_348672,RMVar_hsa_circ_65124,RMVar_hsa_circ_66655,RMVar_hsa_circ_32036 100822 RMVar_ID_100822 Human_SNP_ID_634474889 m1A Human chr17 - 81119386 81119386 81119386 TCACGCACGTGTCTGACTCGGACGCCGAGTCCAAGAGAGGTGAGGCCTGGGCGGGGCTGTGGCAG TCACGCACGTGTCTGACTCGGACGCCGAGTCCGAGAGAGGTGAGGCCTGGGCGGGGCTGTGGCAG T C AATK Ensembl:ENSG00000181409 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81119376..81119534 26863196 MeRIP-seq:(Medium) rs768344838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880033,Human_Splice_Rec_1880059,Human_Splice_Rec_1880069,Human_Splice_Rec_1880099 100823 RMVar_ID_100823 Human_SNP_ID_634474890 m1A Human chr17 - 81119386 81119386 81119386 TCACGCACGTGTCTGACTCGGACGCCGAGTCCAAGAGAGGTGAGGCCTGGGCGGGGCTGTGGCAG TCACGCACGTGTCTGACTCGGACGCCGAGTCCCAGAGAGGTGAGGCCTGGGCGGGGCTGTGGCAG T G AATK Ensembl:ENSG00000181409 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81119376..81119534 26863196 MeRIP-seq:(Medium) rs768344838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880033,Human_Splice_Rec_1880059,Human_Splice_Rec_1880069,Human_Splice_Rec_1880099 100824 RMVar_ID_100824 Human_SNP_ID_634482367 m1A Human chr17 + 81138215 81138213 81138215 ATGCGTGCACACACACACACACCCCCACATGCACACATATCCACCCACACGCACATACCCACACA ATGCGTGCACACACACACACACCCCCACATG__CACATATCCACCCACACGCACATACCCACACA GCA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81138204..81138352 26863196 MeRIP-seq:(Medium) rs777331541 Functional Loss DEL dbSNP153 32..33 33 - - - 100825 RMVar_ID_100825 Human_SNP_ID_634491457 m1A Human chr17 + 81165881 81165881 81165881 CATGCAAACCGGGAGCCGTGGGGCCCAGGGGCATCACGTCCGCAGCGGAGGGAGGCAGCGGCGCG CATGCAAACCGGGAGCCGTGGGGCCCAGGGGCGTCACGTCCGCAGCGGAGGGAGGCAGCGGCGCG A G PVALEF Ensembl:ENSG00000225180 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81165854..81165975 32194978 MeRIP-seq:(Medium) rs896426678 Functional Loss SNV dbSNP153 33..33 33 - - - 100826 RMVar_ID_100826 Human_SNP_ID_634496715 m1A Human chr17 - 81184187 81184187 81184187 GACACCAAGATGAGGAAGGACCTTCAGAGGGTAGAGGTGGAGAGACCAACCAGGGGGCTGTGGTG GACACCAAGATGAGGAAGGACCTTCAGAGGGTGGAGGTGGAGAGACCAACCAGGGGGCTGTGGTG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81184177..81184300 26863196 MeRIP-seq:(Medium) rs1430898330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18711229 100827 RMVar_ID_100827 Human_SNP_ID_634498233 m1A Human chr17 + 81189818 81189818 81189818 TGGGCCTCCTGTGCTGCTCCAGCAGCTCCTCCAGGTGGTCGGCCCGCTTCACCGCAGCCTGCAGC TGGGCCTCCTGTGCTGCTCCAGCAGCTCCTCCGGGTGGTCGGCCCGCTTCACCGCAGCCTGCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81189768..81189894 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 100828 RMVar_ID_100828 Human_SNP_ID_634498542 m1A Human chr17 + 81190663 81190663 81190663 CCGCCCACCTCCGGTGCACCTCCTCCAGCTCCAGCTGCTGGCGGGCCTGCAGCGTGGCCAGCTCG CCGCCCACCTCCGGTGCACCTCCTCCAGCTCCGGCTGCTGGCGGGCCTGCAGCGTGGCCAGCTCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81190652..81190800 26863196 MeRIP-seq:(Medium) rs1484759018 Functional Loss SNV dbSNP153 33..33 33 - - - 100829 RMVar_ID_100829 Human_SNP_ID_634500639 m1A Human chr17 - 81195927 81195927 81195927 CAACACAGCTGATTGAGGACAAGAAGGTCCTGAGTGAAAAGTGCGAGGCTGTGGTGGCCGAGCTG CAACACAGCTGATTGAGGACAAGAAGGTCCTGGGTGAAAAGTGCGAGGCTGTGGTGGCCGAGCTG T C CEP131 Ensembl:ENSG00000141577 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81191310..81197737 32194978 MeRIP-seq:(Medium) rs143331394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18711240 Human_Splice_Rec_1880210,Human_Splice_Rec_1880211,Human_Splice_Rec_1880258,Human_Splice_Rec_1880259,Human_Splice_Rec_1880308,Human_Splice_Rec_1880309,Human_Splice_Rec_1880344,Human_Splice_Rec_1880345,Human_Splice_Rec_1880394,Human_Splice_Rec_1880395 GWAS_ID_13194 RMVar_hsa_circ_86062,RMVar_hsa_circ_187578 100830 RMVar_ID_100830 Human_SNP_ID_634500923 m1A Human chr17 - 81196781 81196780 81196782 ACCTCACGGCCCGGCGGGTCAAGGAGACAGAGAAGGCGCTGAGCCGGCAGCTGCAGCGGCAGAGG ACCTCACGGCCCGGCGGGTCAAGGAGACAGA__AGGCGCTGAGCCGGCAGCTGCAGCGGCAGAGG TTC T CEP131 Ensembl:ENSG00000141577 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81196730..81197040 26863196 MeRIP-seq:(Medium) rs1324079041 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_502377,Human_RBP_ID_27814358 Human_Splice_Rec_1880208,Human_Splice_Rec_1880209,Human_Splice_Rec_1880256,Human_Splice_Rec_1880257,Human_Splice_Rec_1880306,Human_Splice_Rec_1880307,Human_Splice_Rec_1880342,Human_Splice_Rec_1880343,Human_Splice_Rec_1880392,Human_Splice_Rec_1880393 RMVar_hsa_circ_86062,RMVar_hsa_circ_187578 100831 RMVar_ID_100831 Human_SNP_ID_634501018 m1A Human chr17 - 81196961 81196961 81196961 GATGCGGCTGAAGCTGGAGGTGGAGGAGAAGAAGCAGGCCATGCTGCTGCTGCAGAGAGCGCTGG GATGCGGCTGAAGCTGGAGGTGGAGGAGAAGAGGCAGGCCATGCTGCTGCTGCAGAGAGCGCTGG T C CEP131 Ensembl:ENSG00000141577 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81195931..81197833 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_18989502,Human_RBP_ID_26332540,Human_RBP_ID_27814359 Human_Splice_Rec_1880206,Human_Splice_Rec_1880207,Human_Splice_Rec_1880254,Human_Splice_Rec_1880255,Human_Splice_Rec_1880304,Human_Splice_Rec_1880305,Human_Splice_Rec_1880341,Human_Splice_Rec_1880390,Human_Splice_Rec_1880391 RMVar_hsa_circ_86062,RMVar_hsa_circ_187578 100832 RMVar_ID_100832 Human_SNP_ID_634501070 m1A Human chr17 + 81197052 81197052 81197052 CTCCAGGGGCCCCGGCCCCGCCTCCGGCACCCACCCCTGCAGACACAGCCGAGCGTCAGGCGGAA CTCCAGGGGCCCCGGCCCCGCCTCCGGCACCCGCCCCTGCAGACACAGCCGAGCGTCAGGCGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81196926..81197775 26863196 MeRIP-seq:(Medium) rs773106662 Functional Loss SNV dbSNP153 33..33 33 - - - 100833 RMVar_ID_100833 Human_SNP_ID_634501624 m1A Human chr17 + 81198254 81198254 81198254 CCCTGGACTTGGCGCTCCCCCTGCTCGGGGCCATCATCTCCAGGTTGTCCCCAGCTGCATCCTGG CCCTGGACTTGGCGCTCCCCCTGCTCGGGGCCGTCATCTCCAGGTTGTCCCCAGCTGCATCCTGG A G AC027601.3 Ensembl:ENSG00000262115 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81197836..81203892 32194978 MeRIP-seq:(Medium) rs1441226619 Functional Loss SNV dbSNP153 33..33 33 - - - 100834 RMVar_ID_100834 Human_SNP_ID_634508413 m1A Human chr17 + 81219998 81219998 81219998 GGGACACAGGCGGAGGGAGACCTGTCAGACTCAGGTCCACACCTGCTGGGCTGCGCTCCGGGACG GGGACACAGGCGGAGGGAGACCTGTCAGACTCCGGTCCACACCTGCTGGGCTGCGCTCCGGGACG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:81219948..81220118;chr17:81206762..81222900 26863196,32194978 MeRIP-seq:(Medium) rs549998263 Functional Loss SNV dbSNP153 33..33 33 - - - 100835 RMVar_ID_100835 Human_SNP_ID_634508455 m1A Human chr17 - 81220072 81220072 81220072 ATCTCATTGCAGCTCTTGCTTCCCCGCTCAGGACCTGCCTTGTCCACCATGAAAGGCACCCGGGC ATCTCATTGCAGCTCTTGCTTCCCCGCTCAGGTCCTGCCTTGTCCACCATGAAAGGCACCCGGGC T A CEP131 Ensembl:ENSG00000141577 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81219983..81222934 26863410 MeRIP-seq:(Medium) rs1471770547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880182,Human_Splice_Rec_1880230,Human_Splice_Rec_1880280,Human_Splice_Rec_1880366 100836 RMVar_ID_100836 Human_SNP_ID_634511161 m1A Human chr17 + 81229232 81229232 81229232 CCTCGGCCTCGCTGGGGTCTCCGGGGGCTGGAATGGGGGAGGCATCTGGGGGTGGGGTGGGCACA CCTCGGCCTCGCTGGGGTCTCCGGGGGCTGGAGTGGGGGAGGCATCTGGGGGTGGGGTGGGCACA A G AC027601.2 Ensembl:ENSG00000260005 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81229181..81229326 26863196 MeRIP-seq:(Medium) rs1412028838 Functional Loss SNV dbSNP153 33..33 33 - - - 100837 RMVar_ID_100837 Human_SNP_ID_634511509 m1A Human chr17 + 81230260 81230260 81230260 CTTCCTGGAAGAGGTAAGTGTGAGGCCAAGACACAAGGGCAGGAACATTAAGGCAGCGGAGTCTG CTTCCTGGAAGAGGTAAGTGTGAGGCCAAGACCCAAGGGCAGGAACATTAAGGCAGCGGAGTCTG A C AC027601.2 Ensembl:ENSG00000260005 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81230257..81230399 26863196 MeRIP-seq:(Medium) rs61729886 Functional Loss SNV dbSNP153 33..33 33 - - - 100838 RMVar_ID_100838 Human_SNP_ID_634512354 m1A Human chr17 + 81231947 81231947 81231947 GTCCGAGACCCTGCTCAGGTCGCTGTTCTGGGAGGAATTCTGAGAGCTGGGGCCGCTGTCCAGCT GTCCGAGACCCTGCTCAGGTCGCTGTTCTGGGTGGAATTCTGAGAGCTGGGGCCGCTGTCCAGCT A T AC027601.2 Ensembl:ENSG00000260005 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81231898..81231963 26863196 MeRIP-seq:(Medium) rs201738910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880570 100839 RMVar_ID_100839 Human_SNP_ID_634514531 m1A Human chr17 - 81238526 81238526 81238526 CAGAGAACACAGACGTCTCGAAGGGACAGAGAAGGACGCACCATTGTAAGCCCCTCTTAGTAAAC CAGAGAACACAGACGTCTCGAAGGGACAGAGAGGGACGCACCATTGTAAGCCCCTCTTAGTAAAC T C TEPSIN Ensembl:ENSG00000167302 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81238521..81238649 26863196 MeRIP-seq:(Medium) rs1255188640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13194292,Human_RBP_ID_24373546 Human_Splice_Rec_1880537,Human_Splice_Rec_1880549,Human_Splice_Rec_1880553,Human_Splice_Rec_1880555 100840 RMVar_ID_100840 Human_SNP_ID_634514685 m1A Human chr17 - 81239013 81239013 81239013 GGGACCTGGATCATGGCTGCCGCGCCGCCGCTACGGGACCGCCTGAGCTTTCTACACCGGGTGAG GGGACCTGGATCATGGCTGCCGCGCCGCCGCTGCGGGACCGCCTGAGCTTTCTACACCGGGTGAG T C TEPSIN Ensembl:ENSG00000167302 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81238759..81239026 26863196 MeRIP-seq:(Medium) rs1238715100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767274,Human_RBP_ID_9377052,Human_RBP_ID_18419772,Human_RBP_ID_23754364 Human_Splice_Rec_1880431,Human_Splice_Rec_1880451,Human_Splice_Rec_1880493,Human_Splice_Rec_1880547,Human_Splice_Rec_1880557 100841 RMVar_ID_100841 Human_SNP_ID_634514951 m1A Human chr17 + 81239601 81239601 81239601 CCGCGGCGTACGGCAGGTGCGTGCAGGCCTCCACGGCCCCGGGCGGCCGCCTGAGTAAGGACTTC CCGCGGCGTACGGCAGGTGCGTGCAGGCCTCCCCGGCCCCGGGCGGCCGCCTGAGTAAGGACTTC A C NDUFAF8 Ensembl:ENSG00000224877 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:81239385..81239605 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4464883,Human_RBP_ID_18419775,Human_RBP_ID_22443987 Human_Splice_Rec_1880571,Human_Splice_Rec_1880574,Human_Splice_Rec_1880578,Human_Splice_Rec_1880579,Human_Splice_Rec_1880581,Human_Splice_Rec_1880583 100842 RMVar_ID_100842 Human_SNP_ID_634514952 m1A Human chr17 + 81239601 81239601 81239601 CCGCGGCGTACGGCAGGTGCGTGCAGGCCTCCACGGCCCCGGGCGGCCGCCTGAGTAAGGACTTC CCGCGGCGTACGGCAGGTGCGTGCAGGCCTCCGCGGCCCCGGGCGGCCGCCTGAGTAAGGACTTC A G NDUFAF8 Ensembl:ENSG00000224877 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:81239385..81239605 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4464883,Human_RBP_ID_18419775,Human_RBP_ID_22443987 Human_Splice_Rec_1880571,Human_Splice_Rec_1880574,Human_Splice_Rec_1880578,Human_Splice_Rec_1880579,Human_Splice_Rec_1880581,Human_Splice_Rec_1880583 100843 RMVar_ID_100843 Human_SNP_ID_634514963 m1A Human chr17 - 81239620 81239620 81239620 CCTCGAACTCCCGCGCGCAGAAGTCCTTACTCAGGCGGCCGCCCGGGGCCGTGGAGGCCTGCACG CCTCGAACTCCCGCGCGCAGAAGTCCTTACTCGGGCGGCCGCCCGGGGCCGTGGAGGCCTGCACG T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81239351..81239750 26863196 MeRIP-seq:(Medium) rs367877316 Functional Loss SNV dbSNP153 33..33 33 - - - 100844 RMVar_ID_100844 Human_SNP_ID_634515052 m1A Human chr17 - 81239806 81239806 81239806 CGCGGGCTCGTCGATGGCTCGGTGATTTTGTCAGCCGGCGTCTAAAGCACGCGGCAGGCGCTCAA CGCGGGCTCGTCGATGGCTCGGTGATTTTGTCGGCCGGCGTCTAAAGCACGCGGCAGGCGCTCAA T C lnc-TMEM105-1 RNACentral:URS0000D5C750 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81239800..81239899 32194978 MeRIP-seq:(Medium) rs1033453429 Functional Loss SNV dbSNP153 33..33 33 - - - 100845 RMVar_ID_100845 Human_SNP_ID_634515388 m1A Human chr17 + 81240922 81240922 81240922 GGTATTTGGTAGAACACAACGTGTGGTGTGGTAGCTTGCTTTTGAGGCGTATCTAACTTGGAAGC GGTATTTGGTAGAACACAACGTGTGGTGTGGTGGCTTGCTTTTGAGGCGTATCTAACTTGGAAGC A G NDUFAF8 Ensembl:ENSG00000224877 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81240920..81241134 26863410 MeRIP-seq:(Medium) rs59124084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1184881,Human_RBP_ID_3539434,Human_RBP_ID_8465748,Human_RBP_ID_13194333 100846 RMVar_ID_100846 Human_SNP_ID_634517151 m1A Human chr17 - 81245902 81245902 81245902 GCCTGTGTCCCACGAGCAGCCGAGAGGCGGGGAGGACGCTGCTGTCCAGGAGCCCAGGCAGAGGC GCCTGTGTCCCACGAGCAGCCGAGAGGCGGGGGGGACGCTGCTGTCCAGGAGCCCAGGCAGAGGC T C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81245853..81246025 26863196 MeRIP-seq:(Medium) rs75472704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18164015,Human_RBP_ID_22761764 Human_miRNA_ID_2509806,Human_miRNA_ID_2757060 RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_108493,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187590,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_187582 100847 RMVar_ID_100847 Human_SNP_ID_634517282 m1A Human chr17 - 81246159 81246159 81246159 GAAGCCAACTGGCTCGTGGCAGGGCCAGGAGCAGAGACGGGGGACCCTCGCATGAAGCCCAAGCA GAAGCCAACTGGCTCGTGGCAGGGCCAGGAGCCGAGACGGGGGACCCTCGCATGAAGCCCAAGCA T G SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81246108..81246313 26863196 MeRIP-seq:(Medium) rs1165976160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542007,Human_RBP_ID_22959512,Human_RBP_ID_23118978 Human_Splice_Rec_1880618 RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_108493,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187590,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_187582 100848 RMVar_ID_100848 Human_SNP_ID_634517612 m1A Human chr17 - 81246926 81246926 81246926 GGCGGTGATCGAGGAGCAGCACAAGGAGATCCACCAGCAGAGGCAGGAGGACGAGGAGGATAAAC GGCGGTGATCGAGGAGCAGCACAAGGAGATCCGCCAGCAGAGGCAGGAGGACGAGGAGGATAAAC T C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81246876..81247009 26863196 MeRIP-seq:(Medium) rs1214043178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9377054,Human_RBP_ID_17905170 Human_Splice_Rec_1880615,Human_Splice_Rec_1880617,Human_Splice_Rec_1880625,Human_Splice_Rec_1880631,Human_Splice_Rec_1880657 RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_108493,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187590,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582 100849 RMVar_ID_100849 Human_SNP_ID_634517643 m1A Human chr17 - 81247010 81247010 81247010 GCTGGACCACGCCGTCCTGCTTCAGGTGATCAAAGAACAGCAGGTGCAGCAAAAGCGCTTGCTGG GCTGGACCACGCCGTCCTGCTTCAGGTGATCAGAGAACAGCAGGTGCAGCAAAAGCGCTTGCTGG T C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81245546..81247152 32194978 MeRIP-seq:(Medium) rs1158143836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17905871,Human_RBP_ID_22659460,Human_RBP_ID_22740998 Human_Splice_Rec_1880614,Human_Splice_Rec_1880624,Human_Splice_Rec_1880630,Human_Splice_Rec_1880656 Human_miRNA_ID_2513073,Human_miRNA_ID_2751168,Human_miRNA_ID_3055894 RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_108493,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187590,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582 100850 RMVar_ID_100850 Human_SNP_ID_634519480 m1A Human chr17 - 81251575 81251575 81251575 AAGCCTCCCCTCCCAGCGGAGAAGCCGGCTCCAGGGCCTGGGCTGCCGCCCGAGCCTCGCGAGCA AAGCCTCCCCTCCCAGCGGAGAAGCCGGCTCCGGGGCCTGGGCTGCCGCCCGAGCCTCGCGAGCA T C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81251427..81251616 32194978 MeRIP-seq:(Medium) rs1161361468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_902381,Human_RBP_ID_3951311,Human_RBP_ID_5114932,Human_RBP_ID_5319337,Human_RBP_ID_9327523,Human_RBP_ID_22761767 Human_Splice_Rec_1880612,Human_Splice_Rec_1880613,Human_Splice_Rec_1880620,Human_Splice_Rec_1880621,Human_Splice_Rec_1880628,Human_Splice_Rec_1880629,Human_Splice_Rec_1880654,Human_Splice_Rec_1880655,Human_Splice_Rec_1880684 RMVar_hsa_circ_117408,RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_108493,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187590,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187592,RMVar_hsa_circ_187596,RMVar_hsa_circ_87387,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_187591,RMVar_hsa_circ_187599 100851 RMVar_ID_100851 Human_SNP_ID_634519724 m1A Human chr17 - 81252244 81252231 81252244 GGAGGGGAAAAGGCCAAGGGGGGACCGCCGCCAGGCAACGCCGCCGGGGACACAGGGCAGCCCGC GGAGGGGAAAAGGCCAAGGGGGGACCGCCGCC_____________GGGGACACAGGGCAGCCCGC CGGCGGCGTTGCCT C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81252173..81252347 26863196 MeRIP-seq:(Medium) rs928489545 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_6574,Human_RBP_ID_236488,Human_RBP_ID_765751,Human_RBP_ID_820131,Human_RBP_ID_902382,Human_RBP_ID_3542031,Human_RBP_ID_3951313,Human_RBP_ID_5186005,Human_RBP_ID_5368284,Human_RBP_ID_8825078,Human_RBP_ID_9353346,Human_RBP_ID_9422615,Human_RBP_ID_18470163,Human_RBP_ID_22741000,Human_RBP_ID_22761769,Human_RBP_ID_24371586 Human_Splice_Rec_1880611,Human_Splice_Rec_1880619,Human_Splice_Rec_1880627,Human_Splice_Rec_1880653,Human_Splice_Rec_1880683 RMVar_hsa_circ_117408,RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187592,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599 100852 RMVar_ID_100852 Human_SNP_ID_634519881 m1A Human chr17 - 81252502 81252498 81252502 GGCCAGATGGCGCCGCCTCTGCCCGACTCAGAAAGAGAGAAACAAGAGCCGGAGCAGGGAGAGGT GGCCAGATGGCGCCGCCTCTGCCCGACTCAGA____GAGAAACAAGAGCCGGAGCAGGGAGAGGT CTCTT C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81252451..81252625 26863196 MeRIP-seq:(Medium) rs777968247 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_502438,Human_RBP_ID_18989518,Human_RBP_ID_23754394 RMVar_hsa_circ_117408,RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187592,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599 100853 RMVar_ID_100853 Human_SNP_ID_634520112 m1A Human chr17 - 81253151 81253151 81253151 AGGAGAGAGAGGAGCTGGAGCAGGCCCAGATCAAGGGGCCCGTGGATGTGCCTGGACGGGAAGAT AGGAGAGAGAGGAGCTGGAGCAGGCCCAGATCGAGGGGCCCGTGGATGTGCCTGGACGGGAAGAT T C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81253101..81253265;chr17:81253101..81253274 26863196 MeRIP-seq:(Medium) rs778218641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951316,Human_RBP_ID_4480450,Human_RBP_ID_18992765,Human_RBP_ID_20292152,Human_RBP_ID_22443993,Human_RBP_ID_22761775,Human_RBP_ID_26332543 Human_Splice_Rec_1880608,Human_Splice_Rec_1880609,Human_Splice_Rec_1880650,Human_Splice_Rec_1880651,Human_Splice_Rec_1880680,Human_Splice_Rec_1880681 Human_miRNA_ID_2296178,Human_miRNA_ID_2296179 RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599,RMVar_hsa_circ_90875,RMVar_hsa_circ_187600,RMVar_hsa_circ_187601 100854 RMVar_ID_100854 Human_SNP_ID_634520223 m1A Human chr17 - 81253533 81253533 81253533 ATGGAGGTGATGGTAATGGAGGGGACTGTGGGAGAGTGGGTCGGTGGGCTCGTGCCGCCATCTGG ATGGAGGTGATGGTAATGGAGGGGACTGTGGGTGAGTGGGTCGGTGGGCTCGTGCCGCCATCTGG T A SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81253531..81254090 26863196 MeRIP-seq:(Medium) rs552489168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3546671,Human_RBP_ID_5318662,Human_RBP_ID_8092237,Human_RBP_ID_8190521,Human_RBP_ID_9326932,Human_RBP_ID_9423677,Human_RBP_ID_17207022,Human_RBP_ID_18486879,Human_RBP_ID_23276536,Human_RBP_ID_24371587,Human_RBP_ID_26769594,Human_RBP_ID_27572921,Human_RBP_ID_27838612 RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599,RMVar_hsa_circ_90875,RMVar_hsa_circ_187600,RMVar_hsa_circ_187601 100855 RMVar_ID_100855 Human_SNP_ID_634520387 m1A Human chr17 - 81253814 81253799 81253814 TGGTGATGATAGCGGTGATGGTGATGATGGTGACGGTGATGATGATGGTGATGGTGGTAGGGATG TGGTGATGATAGCGGTGATGGTGATGATGGTG_______________GTGATGGTGGTAGGGATG CCATCATCATCACCGT C SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81253808..81254072 26863196 MeRIP-seq:(Medium) rs1355944489 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_23754399 RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599,RMVar_hsa_circ_90875,RMVar_hsa_circ_187600,RMVar_hsa_circ_187601 100856 RMVar_ID_100856 Human_SNP_ID_634522256 m1A Human chr17 - 81260147 81260147 81260147 GGGTCTGGTCCGAGGATTGTGCTTACCTGCTCAGTGGCCTCTGTCCTGTGTGGGTGCAGCCAGCA GGGTCTGGTCCGAGGATTGTGCTTACCTGCTCCGTGGCCTCTGTCCTGTGTGGGTGCAGCCAGCA T G SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81260144..81260375 26863196 MeRIP-seq:(Medium) rs1019615642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262785,Human_RBP_ID_3953202,Human_RBP_ID_5319343,Human_RBP_ID_5368285,Human_RBP_ID_22357476,Human_RBP_ID_24417076 RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599,RMVar_hsa_circ_90875,RMVar_hsa_circ_187600,RMVar_hsa_circ_187601 100857 RMVar_ID_100857 Human_SNP_ID_634522264 m1A Human chr17 + 81260183 81260169 81260183 CAGGTAAGCACAATCCTCGGACCAGACCCAGGAGACACCCAGTGGGCACTTGCCCTGAGAAGGCT CAGGTAAGCACAATCCTCG______________GACACCCAGTGGGCACTTGCCCTGAGAAGGCT GGACCAGACCCAGGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81260179..81260331 26863196 MeRIP-seq:(Medium) rs1056143882 Functional Loss DEL dbSNP153 20..33 33 - - - 100858 RMVar_ID_100858 Human_SNP_ID_634522579 m1A Human chr17 + 81261152 81261152 81261152 CTAGTCCTCCCTCCTTCCCCCGCTCCCCGGCCAATCGTAAGCATCACACGTGCCGCCTCGGTGAC CTAGTCCTCCCTCCTTCCCCCGCTCCCCGGCCGATCGTAAGCATCACACGTGCCGCCTCGGTGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81261145..81261291 26863196 MeRIP-seq:(Medium) rs1359119775 Functional Loss SNV dbSNP153 33..33 33 - - - 100859 RMVar_ID_100859 Human_SNP_ID_634532355 m1A Human chr17 + 81295235 81295235 81295235 CTCGCGGGCCGCCTGTGAATCTCCGAGCCCAGACCCGGAAGAGCCGCAGAGCCAGCTAGGGACAC CTCGCGGGCCGCCTGTGAATCTCCGAGCCCAGGCCCGGAAGAGCCGCAGAGCCAGCTAGGGACAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81295187..81295300 26863196 MeRIP-seq:(Medium) rs1355741322 Functional Loss SNV dbSNP153 33..33 33 - - - 100860 RMVar_ID_100860 Human_SNP_ID_634532360 m1A Human chr17 + 81295241 81295241 81295241 GGCCGCCTGTGAATCTCCGAGCCCAGACCCGGAAGAGCCGCAGAGCCAGCTAGGGACACCTCAGC GGCCGCCTGTGAATCTCCGAGCCCAGACCCGGGAGAGCCGCAGAGCCAGCTAGGGACACCTCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81295190..81295275 26863196 MeRIP-seq:(Medium) rs948861203 Functional Loss SNV dbSNP153 33..33 33 - - - 100861 RMVar_ID_100861 Human_SNP_ID_634535169 m1A Human chr17 + 81304664 81304664 81304664 GTGCGCAGGGAGAAACGTGGCCTTGTTCCCACAGATGCCCACCAGGGTCCCTCACCTGCTCCCCC GTGCGCAGGGAGAAACGTGGCCTTGTTCCCACGGATGCCCACCAGGGTCCCTCACCTGCTCCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81304642..81305054 26863196 MeRIP-seq:(Medium) rs1212207672 Functional Loss SNV dbSNP153 33..33 33 - - - 100862 RMVar_ID_100862 Human_SNP_ID_634535195 m1A Human chr17 - 81304709 81304709 81304709 GGCCGCCTGGTGGGGCAGGCTGGAAGGGGCCAAGGCCAGCGCCAAGGGGGAGCAGGTGAGGGACC GGCCGCCTGGTGGGGCAGGCTGGAAGGGGCCAGGGCCAGCGCCAAGGGGGAGCAGGTGAGGGACC T C LINC00482 Ensembl:ENSG00000185168 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81304704..81304847;chr17:81304700..81304787 26863196 MeRIP-seq:(Medium) rs753419857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8193183 RMVar_hsa_circ_77114,RMVar_hsa_circ_106932,RMVar_hsa_circ_187625,RMVar_hsa_circ_187626 100863 RMVar_ID_100863 Human_SNP_ID_634535450 m1A Human chr17 + 81305205 81305205 81305205 GCCTTCCCTGACGGCTGTGCCCTCCACCAGCCAGGGCCCAGGCACAGCCCCTGAGGCAGGGTGTA GCCTTCCCTGACGGCTGTGCCCTCCACCAGCCTGGGCCCAGGCACAGCCCCTGAGGCAGGGTGTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81305196..81306518 26863196 MeRIP-seq:(Medium) rs1419893506 Functional Loss SNV dbSNP153 33..33 33 - - - 100864 RMVar_ID_100864 Human_SNP_ID_634535517 m1A Human chr17 - 81305339 81305333 81305339 CTGCCCTAGGCCGAGATCCCTGAAGCGGGCCCAGCTCCGTTCACTGCTCCCCCGGCCTCCTGCTG CTGCCCTAGGCCGAGATCCCTGAAGCGGGCCC______GTTCACTGCTCCCCCGGCCTCCTGCTG CGGAGCT C LINC00482 Ensembl:ENSG00000185168 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81305290..81305471 26863196 MeRIP-seq:(Medium) rs1322204143 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_3544120,Human_RBP_ID_5649199,Human_RBP_ID_8191466 Human_Splice_Rec_1880716,Human_Splice_Rec_1880720 Human_miRNA_ID_3096583,Human_miRNA_ID_3214927 RMVar_hsa_circ_77114,RMVar_hsa_circ_106932,RMVar_hsa_circ_187625,RMVar_hsa_circ_187626 100865 RMVar_ID_100865 Human_SNP_ID_634535633 m1A Human chr17 + 81305643 81305643 81305643 CCTAAGCCCAACGACCCTCATCCTTATAAGGGATGGAAGAGGAGGAGAAACTCACATGAGATGAA CCTAAGCCCAACGACCCTCATCCTTATAAGGGTTGGAAGAGGAGGAGAAACTCACATGAGATGAA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81305593..81305780 26863196 MeRIP-seq:(Medium) rs751254363 Functional Loss SNV dbSNP153 33..33 33 - - - 100866 RMVar_ID_100866 Human_SNP_ID_634547145 m1A Human chr17 + 81345699 81345699 81345699 CAGAAGCCACTCCCCGCCCGGCTGCTCGCCCCACGGCCAGTCCCTCCCTCCCCGGCGACGCACCC CAGAAGCCACTCCCCGCCCGGCTGCTCGCCCCCCGGCCAGTCCCTCCCTCCCCGGCGACGCACCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81345609..81345994 26863196 MeRIP-seq:(Medium) rs1022768770 Functional Loss SNV dbSNP153 33..33 33 - - - 100867 RMVar_ID_100867 Human_SNP_ID_634547151 m1A Human chr17 - 81345711 81345711 81345711 GCTGGCTCGGCGGGGTGCGTCGCCGGGGAGGGAGGGACTGGCCGTGGGGCGAGCAGCCGGGCGGG GCTGGCTCGGCGGGGTGCGTCGCCGGGGAGGGGGGGACTGGCCGTGGGGCGAGCAGCCGGGCGGG T C AC027601.6 Ensembl:ENSG00000287431 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81345608..81346010 26863196 MeRIP-seq:(Medium) rs1555636577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5098491,Human_RBP_ID_5115270,Human_RBP_ID_18164035,Human_RBP_ID_18439845,Human_RBP_ID_18460553,Human_RBP_ID_22223258 100868 RMVar_ID_100868 Human_SNP_ID_634560401 m1A Human chr17 + 81388210 81388210 81388210 GCGGTGGCCGTGTTTGGCGCCAGGCGGGAGGCAGCAGTCAGGTGGTCCAGGGGCTGGAGGTGAGG GCGGTGGCCGTGTTTGGCGCCAGGCGGGAGGCGGCAGTCAGGTGGTCCAGGGGCTGGAGGTGAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81388202..81388285 26863196 MeRIP-seq:(Medium) rs1433070640 Functional Loss SNV dbSNP153 33..33 33 - - - 100869 RMVar_ID_100869 Human_SNP_ID_634560552 m1A Human chr17 + 81388645 81388645 81388645 CCTGCCCTTGGGAGCCGTCAGCTGGGGCCACGATGCTGGCAGGGTGAGGCCTGGCAGGGTCTGGG CCTGCCCTTGGGAGCCGTCAGCTGGGGCCACGGTGCTGGCAGGGTGAGGCCTGGCAGGGTCTGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81388350..81388794 26863196 MeRIP-seq:(Medium) rs976137384 Functional Loss SNV dbSNP153 33..33 33 - - - 100870 RMVar_ID_100870 Human_SNP_ID_634560580 m1A Human chr17 + 81388755 81388755 81388755 TTCAGGGTTCCTGCCTGCCTTGAGGATGGGTGATAAGGGGCTGGGCCCTGCCCTCCTGCTGCCTG TTCAGGGTTCCTGCCTGCCTTGAGGATGGGTGGTAAGGGGCTGGGCCCTGCCCTCCTGCTGCCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81388704..81388836 26863196 MeRIP-seq:(Medium) rs1253748450 Functional Loss SNV dbSNP153 33..33 33 - - - 100871 RMVar_ID_100871 Human_SNP_ID_634561451 m1A Human chr17 - 81391329 81391329 81391329 CTAGGGGCCCCTGTTCCCCCACAACCGGGCCCAGCCCTGGAGCCCCCTCCAGCACTCCTCTCCCA CTAGGGGCCCCTGTTCCCCCACAACCGGGCCCGGCCCTGGAGCCCCCTCCAGCACTCCTCTCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81391280..81391412 26863196 MeRIP-seq:(Medium) rs1555643726 Functional Loss SNV dbSNP153 33..33 33 - - - 100872 RMVar_ID_100872 Human_SNP_ID_634562131 m1A Human chr17 - 81393164 81393164 81393164 CCCGGACCCTGGGCAGGGACCCGTCGCCGGGGACCCGCGGAGCCCTCCGGGGATGGAGGAGGCGC CCCGGACCCTGGGCAGGGACCCGTCGCCGGGGTCCCGCGGAGCCCTCCGGGGATGGAGGAGGCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81393117..81393279 26863196 MeRIP-seq:(Medium) rs1357548778 Functional Loss SNV dbSNP153 33..33 33 - - - 100873 RMVar_ID_100873 Human_SNP_ID_634562136 m1A Human chr17 - 81393178 81393178 81393178 GGGAGGGGAAGGTTCCCGGACCCTGGGCAGGGACCCGTCGCCGGGGACCCGCGGAGCCCTCCGGG GGGAGGGGAAGGTTCCCGGACCCTGGGCAGGGTCCCGTCGCCGGGGACCCGCGGAGCCCTCCGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81393103..81393217 26863196 MeRIP-seq:(Medium) rs554958934 Functional Loss SNV dbSNP153 33..33 33 - - - 100874 RMVar_ID_100874 Human_SNP_ID_634563461 m1A Human chr17 - 81396776 81396776 81396776 CCTAGGAGCACAGGGCTCCCTCCCGGGAAGGCAGGGCGTGACCCTGGAGCCGCCGGTCCCTCTTG CCTAGGAGCACAGGGCTCCCTCCCGGGAAGGCGGGGCGTGACCCTGGAGCCGCCGGTCCCTCTTG T C AC110285.6 Ensembl:ENSG00000279692 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81396769..81397138 26863196 MeRIP-seq:(Medium) rs1358843754 Functional Loss SNV dbSNP153 33..33 33 - - - 100875 RMVar_ID_100875 Human_SNP_ID_634564698 m1A Human chr17 + 81399636 81399636 81399636 GCTGACCGGCCCCGCCGCCACCACCGCCTGTGACCCCGGACGCCGCCGCCTCTGCGCCGCCCGCG GCTGACCGGCCCCGCCGCCACCACCGCCTGTGCCCCCGGACGCCGCCGCCTCTGCGCCGCCCGCG A C BAHCC1 Ensembl:ENSG00000266074 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81399431..81399914 26863196 MeRIP-seq:(Medium) rs1352716487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143376,Human_RBP_ID_9326936,Human_RBP_ID_27458657 RMVar_hsa_circ_23210 100876 RMVar_ID_100876 Human_SNP_ID_634565118 m1A Human chr17 + 81400570 81400570 81400570 TGCGGCCCAGCCTCTCAGCCTGCGGCCCGGGGAGGAGGGCAGCGCGGGCGCGGGCTGGGGGTGGC TGCGGCCCAGCCTCTCAGCCTGCGGCCCGGGGTGGAGGGCAGCGCGGGCGCGGGCTGGGGGTGGC A T BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81400563..81400670 26863196 MeRIP-seq:(Medium) rs373369030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23210 100877 RMVar_ID_100877 Human_SNP_ID_634572096 m1A Human chr17 - 81419634 81419634 81419634 GGCGGCTGCACCCGCCGCCTGCGTCAGCTCCCACCCCCGACCCACACCCACTCAGGCTCCCCTCT GGCGGCTGCACCCGCCGCCTGCGTCAGCTCCCCCCCCCGACCCACACCCACTCAGGCTCCCCTCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr17:81419623..81419749;chr17:81419627..81419743 26863196 MeRIP-seq:(Medium) rs1453549436 Functional Loss SNV dbSNP153 33..33 33 - - - 100878 RMVar_ID_100878 Human_SNP_ID_634573887 m1A Human chr17 - 81425243 81425230 81425244 CTATCACCCCCAACCACATCATCACCACTATCACCCCCAACCACATCACCACCAACCACATCACC CTATCACCCCCAACCACATCATCACCACTAT______________TCACCACCAACCACATCACC ATGTGGTTGGGGGTG A lnc-ACTG1-4,lnc-ACTG1-4:2,lnc-ACTG1-4:3,lnc-ACTG1-4:4,lnc-ACTG1-4:5 RNACentral:URS00008B4D47,RNACentral:URS00008B77B2,RNACentral:URS00008B894D,RNACentral:URS00008B76AC,RNACentral:URS00008BB951 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81425239..81425404 26863196 MeRIP-seq:(Medium) rs1555650200 Functional Loss DEL dbSNP153 32..45 33 - - - 100879 RMVar_ID_100879 Human_SNP_ID_634574094 m1A Human chr17 + 81425615 81425604 81425616 TGATAGTGGTGGGTGATGTGGTTGGGGGTGATAGTGGTGGGTGATGTGGTTGGTGGTTATGTGGT TGATAGTGGTGGGTGATGTGGT____________TGGTGGGTGATGTGGTTGGTGGTTATGTGGT TTGGGGGTGATAG T BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81425610..81425784 26863196 MeRIP-seq:(Medium) rs1555650298 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_8941945 RMVar_hsa_circ_23210 100880 RMVar_ID_100880 Human_SNP_ID_634574098 m1A Human chr17 + 81425615 81425612 81425615 TGATAGTGGTGGGTGATGTGGTTGGGGGTGATAGTGGTGGGTGATGTGGTTGGTGGTTATGTGGT TGATAGTGGTGGGTGATGTGGTTGGGGGTG___GTGGTGGGTGATGTGGTTGGTGGTTATGTGGT GATA G BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81425610..81425784 26863196 MeRIP-seq:(Medium) rs1555650303 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8941945 RMVar_hsa_circ_23210 100881 RMVar_ID_100881 Human_SNP_ID_634574099 m1A Human chr17 + 81425615 81425613 81425616 TGATAGTGGTGGGTGATGTGGTTGGGGGTGATAGTGGTGGGTGATGTGGTTGGTGGTTATGTGGT TGATAGTGGTGGGTGATGTGGTTGGGGGTGA___TGGTGGGTGATGTGGTTGGTGGTTATGTGGT ATAG A BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81425610..81425784 26863196 MeRIP-seq:(Medium) rs1555650305 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8941945 RMVar_hsa_circ_23210 100882 RMVar_ID_100882 Human_SNP_ID_634574100 m1A Human chr17 + 81425615 81425615 81425615 TGATAGTGGTGGGTGATGTGGTTGGGGGTGATAGTGGTGGGTGATGTGGTTGGTGGTTATGTGGT TGATAGTGGTGGGTGATGTGGTTGGGGGTGATGGTGGTGGGTGATGTGGTTGGTGGTTATGTGGT A G BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81425610..81425784 26863196 MeRIP-seq:(Medium) rs1249304754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8941945 RMVar_hsa_circ_23210 100883 RMVar_ID_100883 Human_SNP_ID_634574365 m1A Human chr17 - 81426026 81426026 81426026 CACCACCACCACGAGCCACATCACCACCAACCACATCACCCACCATCACCCCCAACCACATCATC CACCACCACCACGAGCCACATCACCACCAACCGCATCACCCACCATCACCCCCAACCACATCATC T C lnc-ACTG1-4,lnc-ACTG1-4:2,lnc-ACTG1-4:3,lnc-ACTG1-4:4,lnc-ACTG1-4:5 RNACentral:URS00008B4549,RNACentral:URS00008B4D47,RNACentral:URS00008B77B2,RNACentral:URS00008B894D,RNACentral:URS00008B76AC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81426022..81426265 26863196 MeRIP-seq:(Medium) rs1555650460 Functional Loss SNV dbSNP153 33..33 33 - - - 100884 RMVar_ID_100884 Human_SNP_ID_634576586 m1A Human chr17 + 81433483 81433483 81433483 GTCATCAGTCCACCGAGGCCCCTCCTGTGCCCAGGGCAGGAGTCATCAGTCCACCGAGGTCCCTG GTCATCAGTCCACCGAGGCCCCTCCTGTGCCCCGGGCAGGAGTCATCAGTCCACCGAGGTCCCTG A C BAHCC1 Ensembl:ENSG00000266074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81433478..81433637 26863196 MeRIP-seq:(Medium) rs1196086950 Functional Loss SNV dbSNP153 33..33 33 - - - 100885 RMVar_ID_100885 Human_SNP_ID_634579642 m1A Human chr17 + 81442644 81442644 81442644 GGACCGGCACCTGGAGGGAACCATGGCCCCCGACCACGCTGCACCCTATGGAGTCTCCTATGCCC GGACCGGCACCTGGAGGGAACCATGGCCCCCGCCCACGCTGCACCCTATGGAGTCTCCTATGCCC A C BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81442574..81442752 26863196 MeRIP-seq:(Medium) rs1461885003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368897 100886 RMVar_ID_100886 Human_SNP_ID_634580473 m1A Human chr17 - 81444435 81444435 81444435 CTCTGCATCATGAGGTGGGGGGCCAGGTCCCCAGGGCAGCTGCTCGGTGGGTGGATCCGGGCGAA CTCTGCATCATGAGGTGGGGGGCCAGGTCCCCTGGGCAGCTGCTCGGTGGGTGGATCCGGGCGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81444367..81444582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 100887 RMVar_ID_100887 Human_SNP_ID_634580474 m1A Human chr17 - 81444435 81444435 81444435 CTCTGCATCATGAGGTGGGGGGCCAGGTCCCCAGGGCAGCTGCTCGGTGGGTGGATCCGGGCGAA CTCTGCATCATGAGGTGGGGGGCCAGGTCCCCGGGGCAGCTGCTCGGTGGGTGGATCCGGGCGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81444367..81444582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 100888 RMVar_ID_100888 Human_SNP_ID_634580989 m1A Human chr17 + 81445400 81445400 81445400 CCAGCACCTGGATCTGGAGGAGCCCGCCCAGGAGAAGGCCCCAAAGTCCACCCACAAGCCAGTTG CCAGCACCTGGATCTGGAGGAGCCCGCCCAGGGGAAGGCCCCAAAGTCCACCCACAAGCCAGTTG A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81445394..81445489 26863196 MeRIP-seq:(Medium) rs369933207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880846,Human_Splice_Rec_1880896 RMVar_hsa_circ_265942,RMVar_hsa_circ_368897 100889 RMVar_ID_100889 Human_SNP_ID_634581099 m1A Human chr17 + 81445591 81445591 81445591 CCCCGTGCACTTTAAATGTCTGCCCTGCCAGCAGCCCCGGGCCTGGCTCCCGGGTGCGCAGCGCC CCCCGTGCACTTTAAATGTCTGCCCTGCCAGCGGCCCCGGGCCTGGCTCCCGGGTGCGCAGCGCC A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81445586..81445666 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_23210136 Human_Splice_Rec_1880847,Human_Splice_Rec_1880897 RMVar_hsa_circ_265942,RMVar_hsa_circ_368897 100890 RMVar_ID_100890 Human_SNP_ID_634583423 m1A Human chr17 + 81451757 81451757 81451757 CCTGGTCCCTGGTGGAGGCCGCTGGCCTGGACAGCTCCACTGCCCCAGCGCAGCCGCCCACAGCC CCTGGTCCCTGGTGGAGGCCGCTGGCCTGGACGGCTCCACTGCCCCAGCGCAGCCGCCCACAGCC A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81451717..81451816 26863196 MeRIP-seq:(Medium) rs782218317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143379 Human_Splice_Rec_1880852,Human_Splice_Rec_1880900 RMVar_hsa_circ_265942 100891 RMVar_ID_100891 Human_SNP_ID_634584791 m1A Human chr17 + 81455355 81455355 81455355 GCGAGCCTGCGAAGAAGCGAAGCAAGCTGGAGAGGAGCGTCTATGCGGGCCTGCAGACTGCCTCC GCGAGCCTGCGAAGAAGCGAAGCAAGCTGGAGTGGAGCGTCTATGCGGGCCTGCAGACTGCCTCC A T BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81455246..81455427;chr17:81455306..81455432 26863196 MeRIP-seq:(Medium) rs782805935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951333,Human_RBP_ID_18992772,Human_RBP_ID_26332545,Human_RBP_ID_27814363 Human_Splice_Rec_1880858,Human_Splice_Rec_1880859,Human_Splice_Rec_1880906,Human_Splice_Rec_1880907 RMVar_hsa_circ_265942 100892 RMVar_ID_100892 Human_SNP_ID_634585624 m1A Human chr17 + 81457591 81457591 81457591 GCCAAGAAGAAGAAGGAGAGGCAGGGGTTGCTAGGTAACCAGGAGGGAGGACAGGGGTTGCTAGG GCCAAGAAGAAGAAGGAGAGGCAGGGGTTGCTGGGTAACCAGGAGGGAGGACAGGGGTTGCTAGG A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81457394..81457618 26863196 MeRIP-seq:(Medium) rs1332849611 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1880861,Human_Splice_Rec_1880909,Human_Splice_Rec_1880935 RMVar_hsa_circ_265942 100893 RMVar_ID_100893 Human_SNP_ID_634585874 m1A Human chr17 - 81458153 81458153 81458153 GGCTGGACAGGCGGCAGGCCCCTGTGGGAAGGAGAGGAGGCCGTCACAGGGGTCCCCATCCTAGA GGCTGGACAGGCGGCAGGCCCCTGTGGGAAGGCGAGGAGGCCGTCACAGGGGTCCCCATCCTAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81458149..81458282 26863196 MeRIP-seq:(Medium) rs782420491 Functional Loss SNV dbSNP153 33..33 33 - - - 100894 RMVar_ID_100894 Human_SNP_ID_634586363 m1A Human chr17 + 81458898 81458898 81458898 CTTTGAGTTCGACGACAACAGCAGCTTCTCGGAAGAGGAGGAGGACGAGGAGGAAGAGGAGGAGG CTTTGAGTTCGACGACAACAGCAGCTTCTCGGGAGAGGAGGAGGACGAGGAGGAAGAGGAGGAGG A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81458848..81458936 26863196 MeRIP-seq:(Medium) rs1227177859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1880866,Human_Splice_Rec_1880867,Human_Splice_Rec_1880914,Human_Splice_Rec_1880915 RMVar_hsa_circ_6024,RMVar_hsa_circ_265942 100895 RMVar_ID_100895 Human_SNP_ID_634602579 m1A Human chr17 + 81510269 81510269 81510269 TTTCCAACCCTGACAGACCCGCAAGACAAAACAACTGGTTCTTGCCAGCCTCTAGAGAAATCCCA TTTCCAACCCTGACAGACCCGCAAGACAAAACTACTGGTTCTTGCCAGCCTCTAGAGAAATCCCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81510137..81510431 26863196 MeRIP-seq:(Medium) rs1421905565 Functional Loss SNV dbSNP153 33..33 33 - - - 100896 RMVar_ID_100896 Human_SNP_ID_634603163 m1A Human chr17 - 81511048 81511048 81511048 CACCTTCAACTCCATCATGAAGTGTGACGTGGACATCCGCAAAGACCTGTACGCCAACACGGTGC CACCTTCAACTCCATCATGAAGTGTGACGTGGGCATCCGCAAAGACCTGTACGCCAACACGGTGC T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs886041756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502513,Human_RBP_ID_763876,Human_RBP_ID_1870691,Human_RBP_ID_8826178,Human_RBP_ID_9078449,Human_RBP_ID_17190229,Human_RBP_ID_17610222,Human_RBP_ID_18191024,Human_RBP_ID_18488154,Human_RBP_ID_23110434,Human_RBP_ID_24532373,Human_RBP_ID_26812870,Human_RBP_ID_27458713 Human_Splice_Rec_1880954,Human_Splice_Rec_1880964,Human_Splice_Rec_1880972,Human_Splice_Rec_1880984,Human_Splice_Rec_1880990,Human_Splice_Rec_1881000,Human_Splice_Rec_1881010,Human_Splice_Rec_1881022,Human_Splice_Rec_1881034,Human_Splice_Rec_1881044 RMVar_hsa_circ_94117,RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_123222,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_112049,RMVar_hsa_circ_187635,RMVar_hsa_circ_187636,RMVar_hsa_circ_187637,RMVar_hsa_circ_376092,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_111725,RMVar_hsa_circ_187639,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_187640 100897 RMVar_ID_100897 Human_SNP_ID_634603507 m1A Human chr17 - 81511623 81511621 81511623 TGACTAAGCCGCCCCTTGTCCCTTCTCAGATTATGTTTGAGACCTTCAACACCCCGGCCATGTAC TGACTAAGCCGCCCCTTGTCCCTTCTCAGATT__GTTTGAGACCTTCAACACCCCGGCCATGTAC CAT C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81511247..81511675 26863410 MeRIP-seq:(Medium) rs1287600431 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_49500,Human_RBP_ID_903229,Human_RBP_ID_1544458,Human_RBP_ID_1870703,Human_RBP_ID_8823422,Human_RBP_ID_20281362,Human_RBP_ID_21975842,Human_RBP_ID_22060207,Human_RBP_ID_22659468,Human_RBP_ID_24481556,Human_RBP_ID_26974461 Human_Splice_Rec_1880952,Human_Splice_Rec_1880962,Human_Splice_Rec_1880970,Human_Splice_Rec_1880980,Human_Splice_Rec_1880988,Human_Splice_Rec_1880998,Human_Splice_Rec_1881008,Human_Splice_Rec_1881020,Human_Splice_Rec_1881032,Human_Splice_Rec_1881050,Human_Splice_Rec_1881056,Human_Splice_Rec_1881062,Human_Splice_Rec_1881068 Human_miRNA_ID_2517633,Human_miRNA_ID_2517634,Human_miRNA_ID_2728281,Human_miRNA_ID_2728282 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_123222,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187636,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_111725,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_187640,RMVar_hsa_circ_81045,RMVar_hsa_circ_321880,RMVar_hsa_circ_187643,RMVar_hsa_circ_187644 100898 RMVar_ID_100898 Human_SNP_ID_634603508 m1A Human chr17 - 81511623 81511623 81511623 TGACTAAGCCGCCCCTTGTCCCTTCTCAGATTATGTTTGAGACCTTCAACACCCCGGCCATGTAC TGACTAAGCCGCCCCTTGTCCCTTCTCAGATTTTGTTTGAGACCTTCAACACCCCGGCCATGTAC T A ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81511247..81511675 26863410 MeRIP-seq:(Medium) rs767493603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49500,Human_RBP_ID_903229,Human_RBP_ID_1544458,Human_RBP_ID_1870703,Human_RBP_ID_8823422,Human_RBP_ID_20281362,Human_RBP_ID_21975842,Human_RBP_ID_22060207,Human_RBP_ID_22659468,Human_RBP_ID_24481556,Human_RBP_ID_26974461 Human_Splice_Rec_1880952,Human_Splice_Rec_1880962,Human_Splice_Rec_1880970,Human_Splice_Rec_1880980,Human_Splice_Rec_1880988,Human_Splice_Rec_1880998,Human_Splice_Rec_1881008,Human_Splice_Rec_1881020,Human_Splice_Rec_1881032,Human_Splice_Rec_1881050,Human_Splice_Rec_1881056,Human_Splice_Rec_1881062,Human_Splice_Rec_1881068 Human_miRNA_ID_2517633,Human_miRNA_ID_2517634,Human_miRNA_ID_2728281,Human_miRNA_ID_2728282 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_123222,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187636,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_111725,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_187640,RMVar_hsa_circ_81045,RMVar_hsa_circ_321880,RMVar_hsa_circ_187643,RMVar_hsa_circ_187644 100899 RMVar_ID_100899 Human_SNP_ID_634603915 m1A Human chr17 + 81512039 81512039 81512039 GCCAGATCTTCTCCATGTCGTCCCAGTTGGTGACGATGCCATGCTCAATGGGGTACTTCAGGGTC GCCAGATCTTCTCCATGTCGTCCCAGTTGGTGGCGATGCCATGCTCAATGGGGTACTTCAGGGTC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:81511937..81512076 26863410 MeRIP-seq:(Medium) rs782204140 Functional Loss SNV dbSNP153 33..33 33 - - - 100900 RMVar_ID_100900 Human_SNP_ID_634603972 m1A Human chr17 - 81512117 81512117 81512117 CCTGCAGGGCGTCATGGTGGGCATGGGCCAGAAGGACTCCTACGTGGGCGACGAGGCCCAGAGCA CCTGCAGGGCGTCATGGTGGGCATGGGCCAGAGGGACTCCTACGTGGGCGACGAGGCCCAGAGCA T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81512066..81512600 26863196 MeRIP-seq:(Medium) rs577515884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49502,Human_RBP_ID_502536,Human_RBP_ID_820951,Human_RBP_ID_897033,Human_RBP_ID_1011056,Human_RBP_ID_1289491,Human_RBP_ID_1544465,Human_RBP_ID_1870707,Human_RBP_ID_4458699,Human_RBP_ID_5362182,Human_RBP_ID_6651185,Human_RBP_ID_8465889,Human_RBP_ID_8823425,Human_RBP_ID_9326949,Human_RBP_ID_17902757,Human_RBP_ID_18191034,Human_RBP_ID_22445081,Human_RBP_ID_22587138,Human_RBP_ID_27156937,Human_RBP_ID_27458746 Human_Splice_Rec_1880950,Human_Splice_Rec_1880960,Human_Splice_Rec_1880968,Human_Splice_Rec_1880978,Human_Splice_Rec_1880996,Human_Splice_Rec_1881006,Human_Splice_Rec_1881018,Human_Splice_Rec_1881028,Human_Splice_Rec_1881040,Human_Splice_Rec_1881054,Human_Splice_Rec_1881060,Human_Splice_Rec_1881066,Human_Splice_Rec_1881072 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_81045,RMVar_hsa_circ_187644,RMVar_hsa_circ_307034 100901 RMVar_ID_100901 Human_SNP_ID_634604086 m1A Human chr17 + 81512263 81512263 81512263 CCTGGTGTCTGGGGCGCCCGACGATGGAAGGAAACACGGCTCGGGGAGCGTCGTCCCCAGCAAAA CCTGGTGTCTGGGGCGCCCGACGATGGAAGGAGACACGGCTCGGGGAGCGTCGTCCCCAGCAAAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81511857..81512390 26863196 MeRIP-seq:(Medium) rs1555667217 Functional Loss SNV dbSNP153 33..33 33 - - - 100902 RMVar_ID_100902 Human_SNP_ID_634604100 m1A Human chr17 + 81512277 81512277 81512277 CGCCCGACGATGGAAGGAAACACGGCTCGGGGAGCGTCGTCCCCAGCAAAACCAGCTTTGCACAT CGCCCGACGATGGAAGGAAACACGGCTCGGGGGGCGTCGTCCCCAGCAAAACCAGCTTTGCACAT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81511851..81512414 26863196 MeRIP-seq:(Medium) rs11549228 Functional Loss SNV dbSNP153 33..33 33 - - - 100903 RMVar_ID_100903 Human_SNP_ID_634604151 m1A Human chr17 - 81512349 81512349 81512349 AGTCCATCCTTTTCCGGGCAGGTCGCAATGGAAGAAGAGATCGCCGCGCTGGTCATTGACAATGG AGTCCATCCTTTTCCGGGCAGGTCGCAATGGAGGAAGAGATCGCCGCGCTGGTCATTGACAATGG T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782546771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502541,Human_RBP_ID_820952,Human_RBP_ID_903233,Human_RBP_ID_1011058,Human_RBP_ID_1184994,Human_RBP_ID_1544470,Human_RBP_ID_1870708,Human_RBP_ID_3539529,Human_RBP_ID_4458702,Human_RBP_ID_5362183,Human_RBP_ID_6651190,Human_RBP_ID_8465894,Human_RBP_ID_8823429,Human_RBP_ID_9326950,Human_RBP_ID_13195052,Human_RBP_ID_17494486,Human_RBP_ID_18711442,Human_RBP_ID_22062911,Human_RBP_ID_22443245,Human_RBP_ID_22656970,Human_RBP_ID_23754603,Human_RBP_ID_26812888 Human_Splice_Rec_1880948,Human_Splice_Rec_1880958,Human_Splice_Rec_1880976,Human_Splice_Rec_1880994,Human_Splice_Rec_1881004,Human_Splice_Rec_1881016,Human_Splice_Rec_1881026,Human_Splice_Rec_1881038,Human_Splice_Rec_1881046,Human_Splice_Rec_1881052,Human_Splice_Rec_1881058,Human_Splice_Rec_1881064,Human_Splice_Rec_1881070 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_27847,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_187642,RMVar_hsa_circ_81045,RMVar_hsa_circ_187644,RMVar_hsa_circ_307034 100904 RMVar_ID_100904 Human_SNP_ID_634604355 m1A Human chr17 + 81512589 81512559 81512589 CGGGCCCCGCCCTGGACCCCCGGCGCCCCCCCAGCCCCGTCCGCCTGACCCGGCCCACCCCGCCT CGG______________________________GCCCCGTCCGCCTGACCCGGCCCACCCCGCCT GGCCCCGCCCTGGACCCCCGGCGCCCCCCCA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81512576..81512700 26863196 MeRIP-seq:(Medium) rs1555667422 Functional Loss DEL dbSNP153 4..33 33 - - - 100905 RMVar_ID_100905 Human_SNP_ID_634604360 m1A Human chr17 + 81512589 81512573 81512590 CGGGCCCCGCCCTGGACCCCCGGCGCCCCCCCAGCCCCGTCCGCCTGACCCGGCCCACCCCGCCT CGGGCCCCGCCCTGGAC_________________CCCCGTCCGCCTGACCCGGCCCACCCCGCCT CCCCCGGCGCCCCCCCAG C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81512576..81512700 26863196 MeRIP-seq:(Medium) rs1304795412 Functional Loss DEL dbSNP153 18..34 33 - - - 100906 RMVar_ID_100906 Human_SNP_ID_634604513 m1A Human chr17 + 81512744 81512744 81512744 GGCCCCGGGGCGGGGCGCTCACCGGCAGAGAAACGCGACGGCGGAGCGGCGGAAGAACAGAGTGC GGCCCCGGGGCGGGGCGCTCACCGGCAGAGAACCGCGACGGCGGAGCGGCGGAAGAACAGAGTGC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81512726..81512800;chr17:81511875..81512800 26863196 MeRIP-seq:(Medium) rs1555667535 Functional Loss SNV dbSNP153 33..33 33 - - - 100907 RMVar_ID_100907 Human_SNP_ID_634604556 m1A Human chr17 + 81512770 81512770 81512770 AGAGAAACGCGACGGCGGAGCGGCGGAAGAACAGAGTGCGAGAGCTGGCAGCGGCGACTGAGACC AGAGAAACGCGACGGCGGAGCGGCGGAAGAACGGAGTGCGAGAGCTGGCAGCGGCGACTGAGACC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81512601..81512800 26863196 MeRIP-seq:(Medium) rs1057522087 Functional Loss SNV dbSNP153 33..33 33 - - - 100908 RMVar_ID_100908 Human_SNP_ID_634604557 m1A Human chr17 + 81512770 81512770 81512770 AGAGAAACGCGACGGCGGAGCGGCGGAAGAACAGAGTGCGAGAGCTGGCAGCGGCGACTGAGACC AGAGAAACGCGACGGCGGAGCGGCGGAAGAACTGAGTGCGAGAGCTGGCAGCGGCGACTGAGACC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81512601..81512800 26863196 MeRIP-seq:(Medium) rs1057522087 Functional Loss SNV dbSNP153 33..33 33 - - - 100909 RMVar_ID_100909 Human_SNP_ID_634604560 m1A Human chr17 + 81512772 81512772 81512772 AGAAACGCGACGGCGGAGCGGCGGAAGAACAGAGTGCGAGAGCTGGCAGCGGCGACTGAGACCGA AGAAACGCGACGGCGGAGCGGCGGAAGAACAGGGTGCGAGAGCTGGCAGCGGCGACTGAGACCGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81512651..81512800 26863196 MeRIP-seq:(Medium) rs1555667563 Functional Loss SNV dbSNP153 33..33 33 - - - 100910 RMVar_ID_100910 Human_SNP_ID_634604579 m1A Human chr17 + 81512780 81512780 81512780 GACGGCGGAGCGGCGGAAGAACAGAGTGCGAGAGCTGGCAGCGGCGACTGAGACCGACCGCGGCC GACGGCGGAGCGGCGGAAGAACAGAGTGCGAGGGCTGGCAGCGGCGACTGAGACCGACCGCGGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated;HTR8/Svneo,Hypoxia IP chr17:81512576..81512800;chr17:81512776..81512800 26863196,32194978 MeRIP-seq:(Medium) rs1309059926 Functional Loss SNV dbSNP153 33..33 33 - - - 100911 RMVar_ID_100911 Human_SNP_ID_634611148 m1A Human chr17 - 81530965 81530965 81530965 GTGTCTTTGGCTTCCATGGAGGAAGCATTCTCACTGCCACTGTCCCACTTACCCCCTTTAACCAC GTGTCTTTGGCTTCCATGGAGGAAGCATTCTCGCTGCCACTGTCCCACTTACCCCCTTTAACCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81530959..81531178 26863196 MeRIP-seq:(Medium) rs542880468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8465908 100912 RMVar_ID_100912 Human_SNP_ID_634611149 m1A Human chr17 - 81530965 81530965 81530965 GTGTCTTTGGCTTCCATGGAGGAAGCATTCTCACTGCCACTGTCCCACTTACCCCCTTTAACCAC GTGTCTTTGGCTTCCATGGAGGAAGCATTCTCCCTGCCACTGTCCCACTTACCCCCTTTAACCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81530959..81531178 26863196 MeRIP-seq:(Medium) rs542880468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8465908 100913 RMVar_ID_100913 Human_SNP_ID_634611609 m1A Human chr17 + 81531525 81531525 81531525 TGATGGTGATGGTGGTGATGGTGATGGTGGTGATGGCGATGGTGGTGATGATGGTGATGGCGATG TGATGGTGATGGTGGTGATGGTGATGGTGGTGGTGGCGATGGTGGTGATGATGGTGATGGCGATG A G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81531523..81531737 26863196 MeRIP-seq:(Medium) rs1309357749 Functional Loss SNV dbSNP153 33..33 33 - - - 100914 RMVar_ID_100914 Human_SNP_ID_634611987 m1A Human chr17 + 81531891 81531887 81531891 TGATGGCGATGATGGTGATGATGGTGATGGCGATGATGGTGATAGTGATGGTGATGATGGTGATG TGATGGCGATGATGGTGATGATGGTGATG____TGATGGTGATAGTGATGGTGATGATGGTGATG GGCGA G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81531362..81532095 26863196 MeRIP-seq:(Medium) rs796439937 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23754630 100915 RMVar_ID_100915 Human_SNP_ID_634611988 m1A Human chr17 + 81531891 81531888 81531891 TGATGGCGATGATGGTGATGATGGTGATGGCGATGATGGTGATAGTGATGGTGATGATGGTGATG TGATGGCGATGATGGTGATGATGGTGATGG___TGATGGTGATAGTGATGGTGATGATGGTGATG GCGA G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81531362..81532095 26863196 MeRIP-seq:(Medium) rs1238872486 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23754630 100916 RMVar_ID_100916 Human_SNP_ID_634611990 m1A Human chr17 + 81531891 81531889 81531892 TGATGGCGATGATGGTGATGATGGTGATGGCGATGATGGTGATAGTGATGGTGATGATGGTGATG TGATGGCGATGATGGTGATGATGGTGATGGC___GATGGTGATAGTGATGGTGATGATGGTGATG CGAT C FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81531362..81532095 26863196 MeRIP-seq:(Medium) rs1568078368 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_23754630 100917 RMVar_ID_100917 Human_SNP_ID_634611990 m1A Human chr17 - 81531892 81531889 81531892 CCATCACCATCATCACCATCACTATCACCATCATCGCCATCACCATCATCACCATCATCGCCATC CCATCACCATCATCACCATCACTATCACCATC___GCCATCACCATCATCACCATCATCGCCATC CGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81531371..81532133 26863196 MeRIP-seq:(Medium) rs1568078368 Functional Loss DEL dbSNP153 33..35 33 - - - 100918 RMVar_ID_100918 Human_SNP_ID_634611993 m1A Human chr17 + 81531891 81531891 81531891 TGATGGCGATGATGGTGATGATGGTGATGGCGATGATGGTGATAGTGATGGTGATGATGGTGATG TGATGGCGATGATGGTGATGATGGTGATGGCGGTGATGGTGATAGTGATGGTGATGATGGTGATG A G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81531362..81532095 26863196 MeRIP-seq:(Medium) rs1254825099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23754630 100919 RMVar_ID_100919 Human_SNP_ID_634611996 m1A Human chr17 - 81531892 81531892 81531892 CCATCACCATCATCACCATCACTATCACCATCATCGCCATCACCATCATCACCATCATCGCCATC CCATCACCATCATCACCATCACTATCACCATCGTCGCCATCACCATCATCACCATCATCGCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81531371..81532133 26863196 MeRIP-seq:(Medium) rs1344255485 Functional Loss SNV dbSNP153 33..33 33 - - - 100920 RMVar_ID_100920 Human_SNP_ID_634612391 m1A Human chr17 + 81532362 81532335 81532362 TGATGGTGATGATGATGATAGTGATGGTGGTGATGGTGATGGTGATGATAGTGATGGCGATGATG TGATGG___________________________TGGTGATGGTGATGATAGTGATGGCGATGATG GTGATGATGATGATAGTGATGGTGGTGA G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81532161..81532450;chr17:81532203..81532440 26863196 MeRIP-seq:(Medium) rs1568079126 Functional Loss DEL dbSNP153 7..33 33 - - - 100921 RMVar_ID_100921 Human_SNP_ID_634612421 m1A Human chr17 + 81532362 81532356 81532362 TGATGGTGATGATGATGATAGTGATGGTGGTGATGGTGATGGTGATGATAGTGATGGCGATGATG TGATGGTGATGATGATGATAGTGATGG______TGGTGATGGTGATGATAGTGATGGCGATGATG GTGGTGA G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81532161..81532450;chr17:81532203..81532440 26863196 MeRIP-seq:(Medium) rs1198786280 Functional Loss DEL dbSNP153 28..33 33 - - - 100922 RMVar_ID_100922 Human_SNP_ID_634612428 m1A Human chr17 + 81532362 81532362 81532362 TGATGGTGATGATGATGATAGTGATGGTGGTGATGGTGATGGTGATGATAGTGATGGCGATGATG TGATGGTGATGATGATGATAGTGATGGTGGTGGTGGTGATGGTGATGATAGTGATGGCGATGATG A G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81532161..81532450;chr17:81532203..81532440 26863196 MeRIP-seq:(Medium) rs1235226365 Functional Loss SNV dbSNP153 33..33 33 - - - 100923 RMVar_ID_100923 Human_SNP_ID_634612660 m1A Human chr17 + 81532581 81532581 81532581 TGGTGATGGTGGTGATGGTGATGGTGGTGATGATAGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGGTGGTGATGGTGATGGTGGTGATGGTAGTGATGGTGATGGTGATGATGGTGATGGTG A G FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81532531..81532696 26863196 MeRIP-seq:(Medium) rs1303439349 Functional Loss SNV dbSNP153 33..33 33 - - - 100924 RMVar_ID_100924 Human_SNP_ID_634620775 m1A Human chr17 + 81552285 81552282 81552285 GGGCTTGCCCGCCGCCAGGCCCCCGAGAGGGCAGCAGAAGCCCGCCAGGTAGCGGACCCGCGGCG GGGCTTGCCCGCCGCCAGGCCCCCGAGAGG___GCAGAAGCCCGCCAGGTAGCGGACCCGCGGCG GGCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81552151..81552312 26863410 MeRIP-seq:(Medium) rs1320976847 Functional Loss DEL dbSNP153 31..33 33 - - - 100925 RMVar_ID_100925 Human_SNP_ID_634622615 m1A Human chr17 - 81557764 81557764 81557764 CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTATTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTTTTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT T A NPLOC4 Ensembl:ENSG00000182446 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81557716..81557783 26863196 MeRIP-seq:(Medium) rs8068511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5319363,Human_RBP_ID_6651229,Human_RBP_ID_18459997,Human_RBP_ID_26456352 GWAS_ID_13195,GWAS_ID_13196,GWAS_ID_13197,GWAS_ID_13198 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_112503,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_97157,RMVar_hsa_circ_109785,RMVar_hsa_circ_187655,RMVar_hsa_circ_187656,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651 100926 RMVar_ID_100926 Human_SNP_ID_634622616 m1A Human chr17 - 81557764 81557764 81557764 CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTATTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTGTTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81557716..81557783 26863196 MeRIP-seq:(Medium) rs8068511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5319363,Human_RBP_ID_6651229,Human_RBP_ID_18459997,Human_RBP_ID_26456352 GWAS_ID_13195,GWAS_ID_13196,GWAS_ID_13197,GWAS_ID_13198 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_112503,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_97157,RMVar_hsa_circ_109785,RMVar_hsa_circ_187655,RMVar_hsa_circ_187656,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651 100927 RMVar_ID_100927 Human_SNP_ID_634623014 m1A Human chr17 + 81558681 81558679 81558682 GACTTTAAAATCCCACCTGGACATCGGGTGAGAGGAGGAGGGCAGGCAGCAAACCGACCTGCAGA GACTTTAAAATCCCACCTGGACATCGGGTGA___GAGGAGGGCAGGCAGCAAACCGACCTGCAGA AGAG A lnc-FSCN2-3 RNACentral:URS00008B33B1 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:81558576..81558682;chr17:81558631..81558782 32194978 MeRIP-seq:(Medium) rs1382898881 Functional Loss DEL dbSNP153 32..34 33 - - - 100928 RMVar_ID_100928 Human_SNP_ID_634623209 m1A Human chr17 - 81559031 81559031 81559031 ATTCTGCAGGCTGAATGCAGTCTCCAGACTGGAAACGCAGAGCGGCTCCTCACGCCTAATCCTGT ATTCTGCAGGCTGAATGCAGTCTCCAGACTGGTAACGCAGAGCGGCTCCTCACGCCTAATCCTGT T A NPLOC4 Ensembl:ENSG00000182446 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:81558880..81559031;chr17:81558880..81559181 32194978 MeRIP-seq:(Medium) rs1184175188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143384,Human_RBP_ID_6651264,Human_RBP_ID_13195329,Human_RBP_ID_17902786,Human_RBP_ID_18711499 Human_miRNA_ID_311787,Human_miRNA_ID_2396126 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_112503,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_97157,RMVar_hsa_circ_109785,RMVar_hsa_circ_187655,RMVar_hsa_circ_187656,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651 100929 RMVar_ID_100929 Human_SNP_ID_634628665 m1A Human chr17 + 81577761 81577761 81577761 CTACTCTGGCACCAGTGCCAACCCTGCTCCCCAAAACCAGGAACCTGGCTTGAGCCTGTGCTCCT CTACTCTGGCACCAGTGCCAACCCTGCTCCCCGAAACCAGGAACCTGGCTTGAGCCTGTGCTCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81577759..81578133 26863196 MeRIP-seq:(Medium) rs1038642906 Functional Loss SNV dbSNP153 33..33 33 - - - 100930 RMVar_ID_100930 Human_SNP_ID_634629085 m1A Human chr17 - 81579487 81579487 81579487 GGGAGGCTGGAGTGGAGACCACCTTTTAGACCAGGAACTTGTGAAGGGGGTGTTGTCCAGGTAGG GGGAGGCTGGAGTGGAGACCACCTTTTAGACCTGGAACTTGTGAAGGGGGTGTTGTCCAGGTAGG T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81579485..81579705 26863196 MeRIP-seq:(Medium) rs1432718890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2526347 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_112503,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_109785,RMVar_hsa_circ_187655,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651,RMVar_hsa_circ_110201,RMVar_hsa_circ_126762,RMVar_hsa_circ_61876,RMVar_hsa_circ_93822,RMVar_hsa_circ_99888,RMVar_hsa_circ_102533,RMVar_hsa_circ_105515,RMVar_hsa_circ_98483,RMVar_hsa_circ_99841,RMVar_hsa_circ_98379,RMVar_hsa_circ_187665,RMVar_hsa_circ_187669,RMVar_hsa_circ_89376,RMVar_hsa_circ_90300,RMVar_hsa_circ_77509,RMVar_hsa_circ_187667,RMVar_hsa_circ_187668,RMVar_hsa_circ_187666,RMVar_hsa_circ_187661,RMVar_hsa_circ_187663,RMVar_hsa_circ_187664,RMVar_hsa_circ_187662,RMVar_hsa_circ_187659,RMVar_hsa_circ_187660,RMVar_hsa_circ_307937,RMVar_hsa_circ_187658,RMVar_hsa_circ_326794,RMVar_hsa_circ_78810,RMVar_hsa_circ_85026,RMVar_hsa_circ_187674,RMVar_hsa_circ_187675,RMVar_hsa_circ_336653,RMVar_hsa_circ_128140,RMVar_hsa_circ_79329,RMVar_hsa_circ_98754,RMVar_hsa_circ_187679,RMVar_hsa_circ_187680,RMVar_hsa_circ_115173,RMVar_hsa_circ_267169,RMVar_hsa_circ_187682,RMVar_hsa_circ_187684,RMVar_hsa_circ_68503,RMVar_hsa_circ_187683 100931 RMVar_ID_100931 Human_SNP_ID_634633155 m1A Human chr17 - 81593803 81593803 81593803 CTGGAGAGCAGCTGGGGCATCAGGCAGTGGGCACTGGGCACCCAGGAGGGGAGCAGAGAACAAAG CTGGAGAGCAGCTGGGGCATCAGGCAGTGGGCGCTGGGCACCCAGGAGGGGAGCAGAGAACAAAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81593752..81593935 26863196 MeRIP-seq:(Medium) rs933567577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6651496,Human_RBP_ID_13196765 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_109785,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651,RMVar_hsa_circ_110201,RMVar_hsa_circ_126762,RMVar_hsa_circ_61876,RMVar_hsa_circ_93822,RMVar_hsa_circ_99888,RMVar_hsa_circ_105515,RMVar_hsa_circ_98483,RMVar_hsa_circ_99841,RMVar_hsa_circ_98379,RMVar_hsa_circ_187665,RMVar_hsa_circ_89376,RMVar_hsa_circ_90300,RMVar_hsa_circ_77509,RMVar_hsa_circ_187667,RMVar_hsa_circ_187668,RMVar_hsa_circ_187666,RMVar_hsa_circ_187661,RMVar_hsa_circ_187663,RMVar_hsa_circ_187664,RMVar_hsa_circ_187662,RMVar_hsa_circ_187659,RMVar_hsa_circ_187660,RMVar_hsa_circ_307937,RMVar_hsa_circ_187658,RMVar_hsa_circ_326794,RMVar_hsa_circ_78810,RMVar_hsa_circ_85026,RMVar_hsa_circ_187674,RMVar_hsa_circ_187675,RMVar_hsa_circ_336653,RMVar_hsa_circ_128140,RMVar_hsa_circ_187690,RMVar_hsa_circ_312476,RMVar_hsa_circ_98754,RMVar_hsa_circ_187679,RMVar_hsa_circ_187680,RMVar_hsa_circ_115173,RMVar_hsa_circ_267169,RMVar_hsa_circ_370171,RMVar_hsa_circ_187684,RMVar_hsa_circ_68503,RMVar_hsa_circ_187683,RMVar_hsa_circ_375272,RMVar_hsa_circ_322270,RMVar_hsa_circ_349701,RMVar_hsa_circ_316534,RMVar_hsa_circ_265271,RMVar_hsa_circ_283586,RMVar_hsa_circ_290265,RMVar_hsa_circ_275594,RMVar_hsa_circ_187692,RMVar_hsa_circ_187693,RMVar_hsa_circ_187691,RMVar_hsa_circ_187686,RMVar_hsa_circ_187688,RMVar_hsa_circ_187689,RMVar_hsa_circ_187687,RMVar_hsa_circ_187685 100932 RMVar_ID_100932 Human_SNP_ID_634637129 m1A Human chr17 + 81606752 81606752 81606752 GGCACTTAGTACAGATGCCATTCGGCCACGGGAGGTGCCCCTCGCACCCTGACTTAATCTTGCAG GGCACTTAGTACAGATGCCATTCGGCCACGGGGGGTGCCCCTCGCACCCTGACTTAATCTTGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81606652..81606761 26863196 MeRIP-seq:(Medium) rs764783455 Functional Loss SNV dbSNP153 33..33 33 - - - 100933 RMVar_ID_100933 Human_SNP_ID_634639000 m1A Human chr17 - 81613272 81613272 81613272 GAGATTCCAGGGTCCTACTTGTGGTGATCTTAATGGGTGAATAAAGGGAAATATTTATAACATGT GAGATTCCAGGGTCCTACTTGTGGTGATCTTAGTGGGTGAATAAAGGGAAATATTTATAACATGT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81613267..81613399 26863196 MeRIP-seq:(Medium) rs747159588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185023,Human_RBP_ID_2526391,Human_RBP_ID_23754913 RMVar_hsa_circ_114254,RMVar_hsa_circ_187650,RMVar_hsa_circ_110201,RMVar_hsa_circ_99888,RMVar_hsa_circ_105515,RMVar_hsa_circ_89376,RMVar_hsa_circ_187661,RMVar_hsa_circ_187659,RMVar_hsa_circ_187660,RMVar_hsa_circ_187658,RMVar_hsa_circ_326794,RMVar_hsa_circ_78810,RMVar_hsa_circ_85026,RMVar_hsa_circ_187674,RMVar_hsa_circ_187675,RMVar_hsa_circ_128140,RMVar_hsa_circ_98754,RMVar_hsa_circ_187679,RMVar_hsa_circ_187680,RMVar_hsa_circ_115173,RMVar_hsa_circ_370171,RMVar_hsa_circ_187684,RMVar_hsa_circ_187683,RMVar_hsa_circ_349701,RMVar_hsa_circ_265271,RMVar_hsa_circ_187686,RMVar_hsa_circ_286968,RMVar_hsa_circ_350536,RMVar_hsa_circ_187685,RMVar_hsa_circ_187698,RMVar_hsa_circ_47411,RMVar_hsa_circ_56442,RMVar_hsa_circ_187701,RMVar_hsa_circ_333603,RMVar_hsa_circ_81590,RMVar_hsa_circ_187700,RMVar_hsa_circ_311109,RMVar_hsa_circ_109451,RMVar_hsa_circ_187703,RMVar_hsa_circ_296279,RMVar_hsa_circ_187702,RMVar_hsa_circ_90842,RMVar_hsa_circ_187708,RMVar_hsa_circ_187709,RMVar_hsa_circ_94465,RMVar_hsa_circ_287750,RMVar_hsa_circ_289203,RMVar_hsa_circ_274960,RMVar_hsa_circ_187711,RMVar_hsa_circ_187712,RMVar_hsa_circ_187713,RMVar_hsa_circ_187710 100934 RMVar_ID_100934 Human_SNP_ID_634640619 m1A Human chr17 - 81618101 81618099 81618101 TCACATCCCAGACGATGGGCGGCCAGGCAGAGAGGCTCCTCACTTCCCAGACGGGGTGGCGGCCG TCACATCCCAGACGATGGGCGGCCAGGCAGAG__GCTCCTCACTTCCCAGACGGGGTGGCGGCCG CCT C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81618099..81618181 26863196 MeRIP-seq:(Medium) rs1392103049 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_114254,RMVar_hsa_circ_187650,RMVar_hsa_circ_110201,RMVar_hsa_circ_105515,RMVar_hsa_circ_89376,RMVar_hsa_circ_187659,RMVar_hsa_circ_187660,RMVar_hsa_circ_187658,RMVar_hsa_circ_326794,RMVar_hsa_circ_78810,RMVar_hsa_circ_85026,RMVar_hsa_circ_187674,RMVar_hsa_circ_187675,RMVar_hsa_circ_98754,RMVar_hsa_circ_187680,RMVar_hsa_circ_370171,RMVar_hsa_circ_187684,RMVar_hsa_circ_349701,RMVar_hsa_circ_187686,RMVar_hsa_circ_286968,RMVar_hsa_circ_350536,RMVar_hsa_circ_187685,RMVar_hsa_circ_187698,RMVar_hsa_circ_47411,RMVar_hsa_circ_56442,RMVar_hsa_circ_187701,RMVar_hsa_circ_333603,RMVar_hsa_circ_81590,RMVar_hsa_circ_187700,RMVar_hsa_circ_311109,RMVar_hsa_circ_109451,RMVar_hsa_circ_187703,RMVar_hsa_circ_296279,RMVar_hsa_circ_187702,RMVar_hsa_circ_90842,RMVar_hsa_circ_187708,RMVar_hsa_circ_187709,RMVar_hsa_circ_94465,RMVar_hsa_circ_287750,RMVar_hsa_circ_289203,RMVar_hsa_circ_187715,RMVar_hsa_circ_187711,RMVar_hsa_circ_187712,RMVar_hsa_circ_187713,RMVar_hsa_circ_313053,RMVar_hsa_circ_281309 100935 RMVar_ID_100935 Human_SNP_ID_634644437 m1A Human chr17 - 81629802 81629802 81629802 CAGTAACCATCATGTTTTGTTTGCAACAGATAATTCGTGTCCAGTCCCCGGATGGAGTGAAGCGG CAGTAACCATCATGTTTTGTTTGCAACAGATAGTTCGTGTCCAGTCCCCGGATGGAGTGAAGCGG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:81629788..81629878 26863410 MeRIP-seq:(Medium) rs752040425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49450,Human_RBP_ID_901108,Human_RBP_ID_2526395,Human_RBP_ID_3953238,Human_RBP_ID_4465774,Human_RBP_ID_8941864,Human_RBP_ID_9377069,Human_RBP_ID_18992803,Human_RBP_ID_21976303,Human_RBP_ID_26333951 Human_Splice_Rec_1881142,Human_Splice_Rec_1881143,Human_Splice_Rec_1881232,Human_Splice_Rec_1881233,Human_Splice_Rec_1881266,Human_Splice_Rec_1881267,Human_Splice_Rec_1881320,Human_Splice_Rec_1881321,Human_Splice_Rec_1881328,Human_Splice_Rec_1881329 RMVar_hsa_circ_105515,RMVar_hsa_circ_89376,RMVar_hsa_circ_187659,RMVar_hsa_circ_187658,RMVar_hsa_circ_326794,RMVar_hsa_circ_85026,RMVar_hsa_circ_187674,RMVar_hsa_circ_187675,RMVar_hsa_circ_98754,RMVar_hsa_circ_187684,RMVar_hsa_circ_349701,RMVar_hsa_circ_286968,RMVar_hsa_circ_187685,RMVar_hsa_circ_187698,RMVar_hsa_circ_47411,RMVar_hsa_circ_187701,RMVar_hsa_circ_333603,RMVar_hsa_circ_81590,RMVar_hsa_circ_187700,RMVar_hsa_circ_311109,RMVar_hsa_circ_109451,RMVar_hsa_circ_187703,RMVar_hsa_circ_296279,RMVar_hsa_circ_187702,RMVar_hsa_circ_90842,RMVar_hsa_circ_187708,RMVar_hsa_circ_187709,RMVar_hsa_circ_94465,RMVar_hsa_circ_287750,RMVar_hsa_circ_187715,RMVar_hsa_circ_187712,RMVar_hsa_circ_187713,RMVar_hsa_circ_281309,RMVar_hsa_circ_109942,RMVar_hsa_circ_300265,RMVar_hsa_circ_187716,RMVar_hsa_circ_187717 100936 RMVar_ID_100936 Human_SNP_ID_634646698 m1A Human chr17 - 81636878 81636878 81636878 TGCGGCGGCCGGGCGGGAGCGGGGACGCCGGGATGAGGCAGCAGATTTGCCGGCCTCGGCCTGTG TGCGGCGGCCGGGCGGGAGCGGGGACGCCGGGGTGAGGCAGCAGATTTGCCGGCCTCGGCCTGTG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81636875..81637075 26863196 MeRIP-seq:(Medium) rs1195518366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19080418 RMVar_hsa_circ_89376,RMVar_hsa_circ_187658,RMVar_hsa_circ_98754,RMVar_hsa_circ_187684,RMVar_hsa_circ_187701,RMVar_hsa_circ_81590,RMVar_hsa_circ_109451,RMVar_hsa_circ_187702,RMVar_hsa_circ_90842,RMVar_hsa_circ_187713 100937 RMVar_ID_100937 Human_SNP_ID_634646726 m1A Human chr17 - 81636947 81636947 81636947 GCAGGCGGCGGCGGCCCGGGGCTCGAGCCCGGAGGCAGGAGCAGCCGCCATGGCCGAGAGCATCG GCAGGCGGCGGCGGCCCGGGGCTCGAGCCCGGCGGCAGGAGCAGCCGCCATGGCCGAGAGCATCG T G NPLOC4 Ensembl:ENSG00000182446 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81636901..81637050 26863410 MeRIP-seq:(Medium) rs1447470266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951358,Human_RBP_ID_4464902,Human_RBP_ID_9327542,Human_RBP_ID_18419777,Human_RBP_ID_22061791,Human_RBP_ID_26769371,Human_RBP_ID_27813222 Human_Splice_Rec_1881141,Human_Splice_Rec_1881231,Human_Splice_Rec_1881265,Human_Splice_Rec_1881341 RMVar_hsa_circ_89376,RMVar_hsa_circ_187658,RMVar_hsa_circ_98754,RMVar_hsa_circ_187684,RMVar_hsa_circ_187701,RMVar_hsa_circ_81590,RMVar_hsa_circ_109451,RMVar_hsa_circ_187702,RMVar_hsa_circ_90842,RMVar_hsa_circ_187713 100938 RMVar_ID_100938 Human_SNP_ID_634646773 m1A Human chr17 + 81637036 81637036 81637036 GCCGCGGCCTCAGCCCCGGCCCCGGCCTCCCTACGCCGCCGCCACCGCCGCTCCAGCTTCGCCCG GCCGCGGCCTCAGCCCCGGCCCCGGCCTCCCTGCGCCGCCGCCACCGCCGCTCCAGCTTCGCCCG A G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:81636940..81637054 26863410 MeRIP-seq:(Medium) rs1470112409 Functional Loss SNV dbSNP153 33..33 33 - - - 100939 RMVar_ID_100939 Human_SNP_ID_634646774 m1A Human chr17 + 81637036 81637036 81637036 GCCGCGGCCTCAGCCCCGGCCCCGGCCTCCCTACGCCGCCGCCACCGCCGCTCCAGCTTCGCCCG GCCGCGGCCTCAGCCCCGGCCCCGGCCTCCCTTCGCCGCCGCCACCGCCGCTCCAGCTTCGCCCG A T RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:81636940..81637054 26863410 MeRIP-seq:(Medium) rs1470112409 Functional Loss SNV dbSNP153 33..33 33 - - - 100940 RMVar_ID_100940 Human_SNP_ID_634650561 m1A Human chr17 + 81648421 81648421 81648421 GATTTCGCTCGGGCTTCGGGTGACTTCGCCGCAGGACCTACCCAGCTCGCTCACTTCGCTCGCTC GATTTCGCTCGGGCTTCGGGTGACTTCGCCGCGGGACCTACCCAGCTCGCTCACTTCGCTCGCTC A G TSPAN10 Ensembl:ENSG00000182612 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81648199..81648599 26863410 MeRIP-seq:(Medium) rs915121581 Functional Loss SNV dbSNP153 33..33 33 - - - 100941 RMVar_ID_100941 Human_SNP_ID_634650568 m1A Human chr17 - 81648452 81648452 81648452 CCCTGCGTTGGGGGCTGGCATGGGGGACGCGGAGCGAGCGAAGTGAGCGAGCTGGGTAGGTCCTG CCCTGCGTTGGGGGCTGGCATGGGGGACGCGGGGCGAGCGAAGTGAGCGAGCTGGGTAGGTCCTG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81648445..81648573 26863196 MeRIP-seq:(Medium) rs946670030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1881327 100942 RMVar_ID_100942 Human_SNP_ID_634655724 m1A Human chr17 - 81665167 81665167 81665167 CCATCCCTGCTGGACTCCCTACCGCAGGACGGAGTCCAGGACGCAGCCGCAGCCTCCTTCCTTCA CCATCCCTGCTGGACTCCCTACCGCAGGACGGTGTCCAGGACGCAGCCGCAGCCTCCTTCCTTCA T A OXLD1 Ensembl:ENSG00000204237 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81665125..81665325 26863196 MeRIP-seq:(Medium) rs1032811016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502617 100943 RMVar_ID_100943 Human_SNP_ID_634655881 m1A Human chr17 + 81665454 81665454 81665454 GCCTGGTGCCGTCCGCACCTGCTTGGGAGCCCACCTCTACGTGGTCTGTCCCGAATTTTCTGCGC GCCTGGTGCCGTCCGCACCTGCTTGGGAGCCCGCCTCTACGTGGTCTGTCCCGAATTTTCTGCGC A G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81665134..81666090 32194978 MeRIP-seq:(Medium) rs1369589362 Functional Loss SNV dbSNP153 33..33 33 - - - 100944 RMVar_ID_100944 Human_SNP_ID_634656075 m1A Human chr17 + 81666001 81666001 81666001 CCAAGCCCCACCACCTCTGAGGGACCAACCGGAAGAATCGCACCACCCTTTATCCAAGTTTCCCT CCAAGCCCCACCACCTCTGAGGGACCAACCGGCAGAATCGCACCACCCTTTATCCAAGTTTCCCT A C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81665999..81666154 26863196 MeRIP-seq:(Medium) rs1046080857 Functional Loss SNV dbSNP153 33..33 33 - - - 100945 RMVar_ID_100945 Human_SNP_ID_634656118 m1A Human chr17 + 81666230 81666205 81666231 ACGGCCAGTCCCCAGAGCCCAGGAGGGCTCGCACACAGGCGCTCGGCAGATACTGAGAAACAGGA ACGGCCAG__________________________ACAGGCGCTCGGCAGATACTGAGAAACAGGA GTCCCCAGAGCCCAGGAGGGCTCGCAC G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81666188..81666488 32194978 MeRIP-seq:(Medium) rs1439932510 Functional Loss DEL dbSNP153 9..34 33 - - - 100946 RMVar_ID_100946 Human_SNP_ID_634656138 m1A Human chr17 - 81666266 81666266 81666266 CCTTGGGAGAGGAAGCAGCCCGGTGAACGGCCACTTTCCTGTTTCTCAGTATCTGCCGAGCGCCT CCTTGGGAGAGGAAGCAGCCCGGTGAACGGCCGCTTTCCTGTTTCTCAGTATCTGCCGAGCGCCT T C OXLD1 Ensembl:ENSG00000204237 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81666216..81666571 26863196 MeRIP-seq:(Medium) rs564933058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767832,Human_RBP_ID_1544596,Human_RBP_ID_5498031,Human_RBP_ID_18439860,Human_RBP_ID_26974649 100947 RMVar_ID_100947 Human_SNP_ID_634656418 m1A Human chr17 + 81666790 81666790 81666790 GGCGTGGAGATGGCGGGAGCTGGTCGCGGAGCAGCGGTGTCCAGGGTGCAGGCGGGTCCTGGGAG GGCGTGGAGATGGCGGGAGCTGGTCGCGGAGCCGCGGTGTCCAGGGTGCAGGCGGGTCCTGGGAG A C CCDC137 Ensembl:ENSG00000185298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81666726..81666938;chr17:81666726..81667038 26863196 MeRIP-seq:(Medium) rs757525320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238258,Human_RBP_ID_767548,Human_RBP_ID_4465778,Human_RBP_ID_6651705,Human_RBP_ID_9377071,Human_RBP_ID_13198076,Human_RBP_ID_22705794,Human_RBP_ID_22959951,Human_RBP_ID_26332555,Human_RBP_ID_27813224 100948 RMVar_ID_100948 Human_SNP_ID_634656419 m1A Human chr17 + 81666790 81666790 81666790 GGCGTGGAGATGGCGGGAGCTGGTCGCGGAGCAGCGGTGTCCAGGGTGCAGGCGGGTCCTGGGAG GGCGTGGAGATGGCGGGAGCTGGTCGCGGAGCGGCGGTGTCCAGGGTGCAGGCGGGTCCTGGGAG A G CCDC137 Ensembl:ENSG00000185298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:81666726..81666938;chr17:81666726..81667038 26863196 MeRIP-seq:(Medium) rs757525320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238258,Human_RBP_ID_767548,Human_RBP_ID_4465778,Human_RBP_ID_6651705,Human_RBP_ID_9377071,Human_RBP_ID_13198076,Human_RBP_ID_22705794,Human_RBP_ID_22959951,Human_RBP_ID_26332555,Human_RBP_ID_27813224 100949 RMVar_ID_100949 Human_SNP_ID_634657565 m1A Human chr17 + 81670321 81670321 81670321 CCCCAAGTTCAAACAGAGGAAGGGGGAGTCTGACGGGGCCTATATCCACCGCATGCAGCAAGAGG CCCCAAGTTCAAACAGAGGAAGGGGGAGTCTGGCGGGGCCTATATCCACCGCATGCAGCAAGAGG A G CCDC137 Ensembl:ENSG00000185298 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81670207..81670347 26863196 MeRIP-seq:(Medium) rs200847273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9377074,Human_RBP_ID_17902824,Human_RBP_ID_18412093,Human_RBP_ID_22500745,Human_RBP_ID_24544955,Human_RBP_ID_24552413,Human_RBP_ID_26332559,Human_RBP_ID_26460009 Human_Splice_Rec_1881402,Human_Splice_Rec_1881412,Human_Splice_Rec_1881426,Human_Splice_Rec_1881436,Human_Splice_Rec_1881438 RMVar_hsa_circ_69045,RMVar_hsa_circ_279437,RMVar_hsa_circ_299897 100950 RMVar_ID_100950 Human_SNP_ID_634658387 m1A Human chr17 + 81672601 81672601 81672601 GGCCCGCCAGCGGATTGTGGAGGAGGAGAGAGAGCGGGCCGTGCAGGCCTACAGAGCGTTGAAGC GGCCCGCCAGCGGATTGTGGAGGAGGAGAGAGCGCGGGCCGTGCAGGCCTACAGAGCGTTGAAGC A C CCDC137 Ensembl:ENSG00000185298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81672551..81672826 26863196 MeRIP-seq:(Medium) rs1346556640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6651717,Human_RBP_ID_18989538,Human_RBP_ID_22061793,Human_RBP_ID_22959515,Human_RBP_ID_27458857 RMVar_hsa_circ_69045 100951 RMVar_ID_100951 Human_SNP_ID_634658425 m1A Human chr17 + 81672643 81672643 81672643 GCAGGCCTACAGAGCGTTGAAGCAGCGGCAGCAGCAGCTGCACGGGGAGCGACCCCACCTCACTT GCAGGCCTACAGAGCGTTGAAGCAGCGGCAGCGGCAGCTGCACGGGGAGCGACCCCACCTCACTT A G CCDC137 Ensembl:ENSG00000185298 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81672592..81672737 26863196 MeRIP-seq:(Medium) rs1311312294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238260,Human_RBP_ID_27458858 RMVar_hsa_circ_69045 100952 RMVar_ID_100952 Human_SNP_ID_634658635 m1A Human chr17 + 81673259 81673259 81673259 ATGATGACAACACATACACTTAAGAAGGTGGGAACCGGGGGCCGGGCGCGGTGGCTCACACCTGT ATGATGACAACACATACACTTAAGAAGGTGGGCACCGGGGGCCGGGCGCGGTGGCTCACACCTGT A C CCDC137 Ensembl:ENSG00000185298 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81673213..81673362 32194978 MeRIP-seq:(Medium) rs543602816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502631,Human_RBP_ID_6651721,Human_RBP_ID_8466069,Human_RBP_ID_18711619,Human_RBP_ID_22060293,Human_RBP_ID_26458433,Human_RBP_ID_27262203,Human_RBP_ID_27458867 100953 RMVar_ID_100953 Human_SNP_ID_634658792 m1A Human chr17 + 81673761 81673761 81673761 TGGAAAGTGAGGAGCACCTCTGCCTGGCCGCCACCCCGTCTGGCAAGTGAGGAGCGCCTCTGCCC TGGAAAGTGAGGAGCACCTCTGCCTGGCCGCCGCCCCGTCTGGCAAGTGAGGAGCGCCTCTGCCC A G CCDC137 Ensembl:ENSG00000185298 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81673710..81673799 26863196 MeRIP-seq:(Medium) rs3208093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17902836 100954 RMVar_ID_100954 Human_SNP_ID_634658793 m1A Human chr17 + 81673761 81673761 81673761 TGGAAAGTGAGGAGCACCTCTGCCTGGCCGCCACCCCGTCTGGCAAGTGAGGAGCGCCTCTGCCC TGGAAAGTGAGGAGCACCTCTGCCTGGCCGCCTCCCCGTCTGGCAAGTGAGGAGCGCCTCTGCCC A T CCDC137 Ensembl:ENSG00000185298 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81673710..81673799 26863196 MeRIP-seq:(Medium) rs3208093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17902836 100955 RMVar_ID_100955 Human_SNP_ID_634661796 m1A Human chr17 - 81683111 81683111 81683111 CGTGGTTTTTCCTATAGGTGGGCACCAATCTTACTGACATCGTGGCACAGAGAAAGATCACCATC CGTGGTTTTTCCTATAGGTGGGCACCAATCTTGCTGACATCGTGGCACAGAGAAAGATCACCATC T C ARL16 Ensembl:ENSG00000214087 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81682998..81683175 26863196 MeRIP-seq:(Medium) rs376304403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4480667,Human_RBP_ID_13198346,Human_RBP_ID_24373570 Human_Splice_Rec_1881448,Human_Splice_Rec_1881449,Human_Splice_Rec_1881454,Human_Splice_Rec_1881455,Human_Splice_Rec_1881466,Human_Splice_Rec_1881467,Human_Splice_Rec_1881472,Human_Splice_Rec_1881473,Human_Splice_Rec_1881478,Human_Splice_Rec_1881486,Human_Splice_Rec_1881487,Human_Splice_Rec_1881492,Human_Splice_Rec_1881493,Human_Splice_Rec_1881498,Human_Splice_Rec_1881499,Human_Splice_Rec_1881504,Human_Splice_Rec_1881505,Human_Splice_Rec_1881511,Human_Splice_Rec_1881518,Human_Splice_Rec_1881520 RMVar_hsa_circ_187720,RMVar_hsa_circ_75999,RMVar_hsa_circ_114521,RMVar_hsa_circ_87560,RMVar_hsa_circ_187721,RMVar_hsa_circ_187719 100956 RMVar_ID_100956 Human_SNP_ID_634661804 m1A Human chr17 + 81683125 81683125 81683125 TCTGTGCCACGATGTCAGTAAGATTGGTGCCCACCTATAGGAAAAACCACGATGCAAAAAGAACA TCTGTGCCACGATGTCAGTAAGATTGGTGCCCGCCTATAGGAAAAACCACGATGCAAAAAGAACA A G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81683076..81683150 26863196 MeRIP-seq:(Medium) rs141445294 Functional Loss SNV dbSNP153 33..33 33 - - - 100957 RMVar_ID_100957 Human_SNP_ID_634662074 m1A Human chr17 - 81683652 81683652 81683652 CCGCGCGGGGACGGGACCGGGGCGCGGGGGGCACCCGGAGTGGGGCGGGGACTCACCCTTTAGCT CCGCGCGGGGACGGGACCGGGGCGCGGGGGGCTCCCGGAGTGGGGCGGGGACTCACCCTTTAGCT T A ARL16 Ensembl:ENSG00000214087 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81683555..81683693 26863196 MeRIP-seq:(Medium) rs767555748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898038,Human_RBP_ID_5365278,Human_RBP_ID_18420325,Human_RBP_ID_26782893 Human_Splice_Rec_1881461,Human_Splice_Rec_1881491,Human_Splice_Rec_1881503,Human_Splice_Rec_1881519 RMVar_hsa_circ_87560,RMVar_hsa_circ_187721 100958 RMVar_ID_100958 Human_SNP_ID_634662075 m1A Human chr17 - 81683652 81683652 81683652 CCGCGCGGGGACGGGACCGGGGCGCGGGGGGCACCCGGAGTGGGGCGGGGACTCACCCTTTAGCT CCGCGCGGGGACGGGACCGGGGCGCGGGGGGCGCCCGGAGTGGGGCGGGGACTCACCCTTTAGCT T C ARL16 Ensembl:ENSG00000214087 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81683555..81683693 26863196 MeRIP-seq:(Medium) rs767555748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898038,Human_RBP_ID_5365278,Human_RBP_ID_18420325,Human_RBP_ID_26782893 Human_Splice_Rec_1881461,Human_Splice_Rec_1881491,Human_Splice_Rec_1881503,Human_Splice_Rec_1881519 RMVar_hsa_circ_87560,RMVar_hsa_circ_187721 100959 RMVar_ID_100959 Human_SNP_ID_634662408 m1A Human chr17 + 81684085 81684085 81684085 GGCTGGAGGTCGCCATGGGGCGAGGCAGCGGCACCTTCGAGCGTCTCCTAGGTAACGCGTCCCCA GGCTGGAGGTCGCCATGGGGCGAGGCAGCGGCGCCTTCGAGCGTCTCCTAGGTAACGCGTCCCCA A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:81684055..81684142 26863410 MeRIP-seq:(Medium) rs1240623398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238261,Human_RBP_ID_901119,Human_RBP_ID_4459171,Human_RBP_ID_5115274,Human_RBP_ID_5365279,Human_RBP_ID_18419779,Human_RBP_ID_19080429,Human_RBP_ID_20291741,Human_RBP_ID_27838625 Human_Splice_Rec_1881529,Human_Splice_Rec_1881539,Human_Splice_Rec_1881553,Human_Splice_Rec_1881593 100960 RMVar_ID_100960 Human_SNP_ID_634663285 m1A Human chr17 + 81686350 81686350 81686350 ATATGCTGTGAATTCCATCAAGAAGAAAGTCAACGACAAGAACCCACACGTCGCCTTGTATGCCC ATATGCTGTGAATTCCATCAAGAAGAAAGTCACCGACAAGAACCCACACGTCGCCTTGTATGCCC A C HGS Ensembl:ENSG00000185359 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81686301..81686350 26863196 MeRIP-seq:(Medium) rs191034091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1239173,Human_RBP_ID_1544663,Human_RBP_ID_1870847,Human_RBP_ID_2526420,Human_RBP_ID_3539667,Human_RBP_ID_3953243,Human_RBP_ID_5577996,Human_RBP_ID_8253809,Human_RBP_ID_8466098,Human_RBP_ID_13198459,Human_RBP_ID_18531901,Human_RBP_ID_18711641,Human_RBP_ID_18992817 Human_Splice_Rec_1881524,Human_Splice_Rec_1881525,Human_Splice_Rec_1881532,Human_Splice_Rec_1881533,Human_Splice_Rec_1881542,Human_Splice_Rec_1881543,Human_Splice_Rec_1881556,Human_Splice_Rec_1881557,Human_Splice_Rec_1881596,Human_Splice_Rec_1881597,Human_Splice_Rec_1881614,Human_Splice_Rec_1881615,Human_Splice_Rec_1881619 RMVar_hsa_circ_63128,RMVar_hsa_circ_14992,RMVar_hsa_circ_108266,RMVar_hsa_circ_322769,RMVar_hsa_circ_318253,RMVar_hsa_circ_73768,RMVar_hsa_circ_318719,RMVar_hsa_circ_187722,RMVar_hsa_circ_187723,RMVar_hsa_circ_356496,RMVar_hsa_circ_372491,RMVar_hsa_circ_97465,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187724,RMVar_hsa_circ_187726,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_187725 100961 RMVar_ID_100961 Human_SNP_ID_634663286 m1A Human chr17 + 81686350 81686350 81686350 ATATGCTGTGAATTCCATCAAGAAGAAAGTCAACGACAAGAACCCACACGTCGCCTTGTATGCCC ATATGCTGTGAATTCCATCAAGAAGAAAGTCAGCGACAAGAACCCACACGTCGCCTTGTATGCCC A G HGS Ensembl:ENSG00000185359 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81686301..81686350 26863196 MeRIP-seq:(Medium) rs191034091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1239173,Human_RBP_ID_1544663,Human_RBP_ID_1870847,Human_RBP_ID_2526420,Human_RBP_ID_3539667,Human_RBP_ID_3953243,Human_RBP_ID_5577996,Human_RBP_ID_8253809,Human_RBP_ID_8466098,Human_RBP_ID_13198459,Human_RBP_ID_18531901,Human_RBP_ID_18711641,Human_RBP_ID_18992817 Human_Splice_Rec_1881524,Human_Splice_Rec_1881525,Human_Splice_Rec_1881532,Human_Splice_Rec_1881533,Human_Splice_Rec_1881542,Human_Splice_Rec_1881543,Human_Splice_Rec_1881556,Human_Splice_Rec_1881557,Human_Splice_Rec_1881596,Human_Splice_Rec_1881597,Human_Splice_Rec_1881614,Human_Splice_Rec_1881615,Human_Splice_Rec_1881619 RMVar_hsa_circ_63128,RMVar_hsa_circ_14992,RMVar_hsa_circ_108266,RMVar_hsa_circ_322769,RMVar_hsa_circ_318253,RMVar_hsa_circ_73768,RMVar_hsa_circ_318719,RMVar_hsa_circ_187722,RMVar_hsa_circ_187723,RMVar_hsa_circ_356496,RMVar_hsa_circ_372491,RMVar_hsa_circ_97465,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187724,RMVar_hsa_circ_187726,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_187725 100962 RMVar_ID_100962 Human_SNP_ID_634664932 m1A Human chr17 + 81690679 81690679 81690679 GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCAGACTGGGTGGACGCTGAGGAATGCCACCGCTG GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCGGACTGGGTGGACGCTGAGGAATGCCACCGCTG A G HGS Ensembl:ENSG00000185359 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81690676..81690750 26863196 MeRIP-seq:(Medium) rs757934791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237025,Human_RBP_ID_821600,Human_RBP_ID_897051,Human_RBP_ID_2526422,Human_RBP_ID_3953249,Human_RBP_ID_5365300,Human_RBP_ID_9346448,Human_RBP_ID_18470174,Human_RBP_ID_18711649,Human_RBP_ID_18992825,Human_RBP_ID_22543888,Human_RBP_ID_22657008,Human_RBP_ID_22740409,Human_RBP_ID_26332566,Human_RBP_ID_27814377 Human_Splice_Rec_1881550,Human_Splice_Rec_1881551,Human_Splice_Rec_1881564,Human_Splice_Rec_1881565,Human_Splice_Rec_1881604,Human_Splice_Rec_1881605,Human_Splice_Rec_1881626 RMVar_hsa_circ_3701,RMVar_hsa_circ_63128,RMVar_hsa_circ_14992,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_82800,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_187734,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735 100963 RMVar_ID_100963 Human_SNP_ID_634664933 m1A Human chr17 + 81690679 81690679 81690679 GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCAGACTGGGTGGACGCTGAGGAATGCCACCGCTG GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCTGACTGGGTGGACGCTGAGGAATGCCACCGCTG A T HGS Ensembl:ENSG00000185359 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81690676..81690750 26863196 MeRIP-seq:(Medium) rs757934791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237025,Human_RBP_ID_821600,Human_RBP_ID_897051,Human_RBP_ID_2526422,Human_RBP_ID_3953249,Human_RBP_ID_5365300,Human_RBP_ID_9346448,Human_RBP_ID_18470174,Human_RBP_ID_18711649,Human_RBP_ID_18992825,Human_RBP_ID_22543888,Human_RBP_ID_22657008,Human_RBP_ID_22740409,Human_RBP_ID_26332566,Human_RBP_ID_27814377 Human_Splice_Rec_1881550,Human_Splice_Rec_1881551,Human_Splice_Rec_1881564,Human_Splice_Rec_1881565,Human_Splice_Rec_1881604,Human_Splice_Rec_1881605,Human_Splice_Rec_1881626 RMVar_hsa_circ_3701,RMVar_hsa_circ_63128,RMVar_hsa_circ_14992,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_82800,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_187734,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735 100964 RMVar_ID_100964 Human_SNP_ID_634665219 m1A Human chr17 + 81691438 81691438 81691438 CCCCAGTGCCTGTGACCAGGCCCGCCCGCCCCATCTTACAGCACCACTGCCGGGCGTGTGGGCAG CCCCAGTGCCTGTGACCAGGCCCGCCCGCCCCGTCTTACAGCACCACTGCCGGGCGTGTGGGCAG A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81691426..81691500 32194978 MeRIP-seq:(Medium) rs760017392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897054,Human_RBP_ID_26782895 RMVar_hsa_circ_3701,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735 100965 RMVar_ID_100965 Human_SNP_ID_634665235 m1A Human chr17 + 81691504 81691504 81691504 TATTCTGTGGAAAGTGTTCTTCCAAGTACTCCACCATCCCCAAGTTTGGCATCGAGAAGGAGGTG TATTCTGTGGAAAGTGTTCTTCCAAGTACTCCGCCATCCCCAAGTTTGGCATCGAGAAGGAGGTG A G HGS Ensembl:ENSG00000185359 Protein coding exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr17:81691426..81691550;chr17:81691426..81691607 26863196 MeRIP-seq:(Medium) rs755902337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1544671,Human_RBP_ID_1870849,Human_RBP_ID_3951363,Human_RBP_ID_9377082,Human_RBP_ID_17494502,Human_RBP_ID_18989545 Human_Splice_Rec_1881552,Human_Splice_Rec_1881566,Human_Splice_Rec_1881567,Human_Splice_Rec_1881606,Human_Splice_Rec_1881607 Human_miRNA_ID_1957620 RMVar_hsa_circ_3701,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735,RMVar_hsa_circ_33811,RMVar_hsa_circ_342586 100966 RMVar_ID_100966 Human_SNP_ID_634665241 m1A Human chr17 + 81691514 81691514 81691514 AAAGTGTTCTTCCAAGTACTCCACCATCCCCAAGTTTGGCATCGAGAAGGAGGTGCGCGTGTGTG AAAGTGTTCTTCCAAGTACTCCACCATCCCCAGGTTTGGCATCGAGAAGGAGGTGCGCGTGTGTG A G HGS Ensembl:ENSG00000185359 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81691426..81691605 26863196 MeRIP-seq:(Medium) rs950848061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951363,Human_RBP_ID_9377082,Human_RBP_ID_17494502,Human_RBP_ID_18989545,Human_RBP_ID_22807266 Human_Splice_Rec_1881552,Human_Splice_Rec_1881566,Human_Splice_Rec_1881567,Human_Splice_Rec_1881606,Human_Splice_Rec_1881607 Human_miRNA_ID_2016997 RMVar_hsa_circ_3701,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735,RMVar_hsa_circ_33811,RMVar_hsa_circ_342586 100967 RMVar_ID_100967 Human_SNP_ID_634665965 m1A Human chr17 - 81693553 81693553 81693553 GTACCTGGGACTGCTGAGACAGGGGGCTGGTCAGGTACTCGGGGGGCAGCTCAGTGGTGGAAGTG GTACCTGGGACTGCTGAGACAGGGGGCTGGTCGGGTACTCGGGGGGCAGCTCAGTGGTGGAAGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81693459..81693775 26863196 MeRIP-seq:(Medium) rs144747412 Functional Loss SNV dbSNP153 33..33 33 - - - 100968 RMVar_ID_100968 Human_SNP_ID_634665968 m1A Human chr17 + 81693558 81693558 81693558 CCACCACTGAGCTGCCCCCCGAGTACCTGACCAGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC CCACCACTGAGCTGCCCCCCGAGTACCTGACCCGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC A C HGS Ensembl:ENSG00000185359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:81693458..81693775;chr17:81693481..81693775 26863196 MeRIP-seq:(Medium) rs762551677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904235,Human_RBP_ID_3951364,Human_RBP_ID_5365310,Human_RBP_ID_8466100,Human_RBP_ID_18992830,Human_RBP_ID_19080441,Human_RBP_ID_24373575 Human_Splice_Rec_1881568,Human_Splice_Rec_1881569,Human_Splice_Rec_1881608,Human_Splice_Rec_1881609 Human_miRNA_ID_272329 RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_21404,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_123553,RMVar_hsa_circ_342586,RMVar_hsa_circ_328249,RMVar_hsa_circ_97811,RMVar_hsa_circ_187738,RMVar_hsa_circ_187739 100969 RMVar_ID_100969 Human_SNP_ID_634665969 m1A Human chr17 + 81693558 81693558 81693558 CCACCACTGAGCTGCCCCCCGAGTACCTGACCAGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC CCACCACTGAGCTGCCCCCCGAGTACCTGACCGGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC A G HGS Ensembl:ENSG00000185359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:81693458..81693775;chr17:81693481..81693775 26863196 MeRIP-seq:(Medium) rs762551677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904235,Human_RBP_ID_3951364,Human_RBP_ID_5365310,Human_RBP_ID_8466100,Human_RBP_ID_18992830,Human_RBP_ID_19080441,Human_RBP_ID_24373575 Human_Splice_Rec_1881568,Human_Splice_Rec_1881569,Human_Splice_Rec_1881608,Human_Splice_Rec_1881609 Human_miRNA_ID_272329 RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_21404,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_123553,RMVar_hsa_circ_342586,RMVar_hsa_circ_328249,RMVar_hsa_circ_97811,RMVar_hsa_circ_187738,RMVar_hsa_circ_187739 100970 RMVar_ID_100970 Human_SNP_ID_634665990 m1A Human chr17 - 81693567 81693567 81693567 ACGGAGGGGGCTGAGTACCTGGGACTGCTGAGACAGGGGGCTGGTCAGGTACTCGGGGGGCAGCT ACGGAGGGGGCTGAGTACCTGGGACTGCTGAGTCAGGGGGCTGGTCAGGTACTCGGGGGGCAGCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81693551..81693600 26863196 MeRIP-seq:(Medium) rs372459550 Functional Loss SNV dbSNP153 33..33 33 - - - 100971 RMVar_ID_100971 Human_SNP_ID_634665991 m1A Human chr17 - 81693567 81693567 81693567 ACGGAGGGGGCTGAGTACCTGGGACTGCTGAGACAGGGGGCTGGTCAGGTACTCGGGGGGCAGCT ACGGAGGGGGCTGAGTACCTGGGACTGCTGAGGCAGGGGGCTGGTCAGGTACTCGGGGGGCAGCT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81693551..81693600 26863196 MeRIP-seq:(Medium) rs372459550 Functional Loss SNV dbSNP153 33..33 33 - - - 100972 RMVar_ID_100972 Human_SNP_ID_634666001 m1A Human chr17 - 81693576 81693576 81693576 GCCCACGGGACGGAGGGGGCTGAGTACCTGGGACTGCTGAGACAGGGGGCTGGTCAGGTACTCGG GCCCACGGGACGGAGGGGGCTGAGTACCTGGGGCTGCTGAGACAGGGGGCTGGTCAGGTACTCGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81693526..81693779 26863196 MeRIP-seq:(Medium) rs759041948 Functional Loss SNV dbSNP153 33..33 33 - - - 100973 RMVar_ID_100973 Human_SNP_ID_634666120 m1A Human chr17 - 81693754 81693754 81693754 CCCTCCTGAGGCCGCCCCGCCCCACCCGGCTTACCAGCCTCTCCTTCTCCTCCGCCTCTGACTGT CCCTCCTGAGGCCGCCCCGCCCCACCCGGCTTCCCAGCCTCTCCTTCTCCTCCGCCTCTGACTGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:81693727..81693945;chr17:81693651..81694893 32194978 MeRIP-seq:(Medium) rs754587948 Functional Loss SNV dbSNP153 33..33 33 - - - 100974 RMVar_ID_100974 Human_SNP_ID_634666188 m1A Human chr17 - 81693853 81693853 81693853 ACGTGGACTTCTGTCTCTGAGGCAGAATCAGAAGGGGCGTCACTTGGGTGCACGTGACGCCCCTC ACGTGGACTTCTGTCTCTGAGGCAGAATCAGAGGGGGCGTCACTTGGGTGCACGTGACGCCCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81693851..81693950;chr17:81693851..81693925 26863196 MeRIP-seq:(Medium) rs762241147 Functional Loss SNV dbSNP153 33..33 33 - - - 100975 RMVar_ID_100975 Human_SNP_ID_634666899 m1A Human chr17 + 81695697 81695697 81695697 ATAAGGAGCAGATGGACTCTGCTCCAGGCTTGAGTATAGCTGGGTGCCTCCATCCCAGGCCCCAC ATAAGGAGCAGATGGACTCTGCTCCAGGCTTGGGTATAGCTGGGTGCCTCCATCCCAGGCCCCAC A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81695694..81696142 32194978 MeRIP-seq:(Medium) rs906049728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322769,RMVar_hsa_circ_17845,RMVar_hsa_circ_116462,RMVar_hsa_circ_187731,RMVar_hsa_circ_21404,RMVar_hsa_circ_87300,RMVar_hsa_circ_187737,RMVar_hsa_circ_123553,RMVar_hsa_circ_123682,RMVar_hsa_circ_187739,RMVar_hsa_circ_89961,RMVar_hsa_circ_187745,RMVar_hsa_circ_187746,RMVar_hsa_circ_62740,RMVar_hsa_circ_369899,RMVar_hsa_circ_187748 100976 RMVar_ID_100976 Human_SNP_ID_634667261 m1A Human chr17 - 81696510 81696510 81696510 GCAGCCACTGCACCTGCTTCTTCTGCCGCATTATCTCCAGCTTCTGGGCCAGCTGGATCTGGCGC GCAGCCACTGCACCTGCTTCTTCTGCCGCATTGTCTCCAGCTTCTGGGCCAGCTGGATCTGGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81696349..81696698 26863196 MeRIP-seq:(Medium) rs760895123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18711663 100977 RMVar_ID_100977 Human_SNP_ID_634668967 m1A Human chr17 - 81700816 81700816 81700816 CCTGGCCCCCAGCAGGGCCTGGAGGTCACTGTACCTGCATGTTGTAAGGCTGGTAGCCCATGGAG CCTGGCCCCCAGCAGGGCCTGGAGGTCACTGTGCCTGCATGTTGTAAGGCTGGTAGCCCATGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81700782..81701274 32194978 MeRIP-seq:(Medium) rs1294156586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1544698 100978 RMVar_ID_100978 Human_SNP_ID_634669098 m1A Human chr17 + 81701120 81701120 81701120 CCCAGCAGCCCTACATCGCGGGGCAGCAGCCCATGTACCAGCAGGTGAGCCATTCCCGGGGCCTC CCCAGCAGCCCTACATCGCGGGGCAGCAGCCCGTGTACCAGCAGGTGAGCCATTCCCGGGGCCTC A G HGS Ensembl:ENSG00000185359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81701024..81701145 26863196 MeRIP-seq:(Medium) rs1190264087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951374,Human_RBP_ID_18164044,Human_RBP_ID_26330918 Human_Splice_Rec_1881590,Human_Splice_Rec_1881591,Human_Splice_Rec_1881656,Human_Splice_Rec_1881660,Human_Splice_Rec_1881661,Human_Splice_Rec_1881664,Human_Splice_Rec_1881665,Human_Splice_Rec_1881667 RMVar_hsa_circ_7668,RMVar_hsa_circ_322769,RMVar_hsa_circ_17845,RMVar_hsa_circ_116462,RMVar_hsa_circ_187731,RMVar_hsa_circ_21404,RMVar_hsa_circ_87300,RMVar_hsa_circ_187737,RMVar_hsa_circ_123682,RMVar_hsa_circ_89961,RMVar_hsa_circ_187745,RMVar_hsa_circ_187746,RMVar_hsa_circ_62740,RMVar_hsa_circ_187751,RMVar_hsa_circ_285456,RMVar_hsa_circ_124267,RMVar_hsa_circ_187750,RMVar_hsa_circ_69142 100979 RMVar_ID_100979 Human_SNP_ID_634669403 m1A Human chr17 - 81701684 81701669 81701684 GGCAGTAGAGGACAGGGAGGCAGGACGACGGCAGTTAGAGACGAGGCGTTTCAGGTGAACTGTAT GGCAGTAGAGGACAGGGAGGCAGGACGACGGC_______________GTTTCAGGTGAACTGTAT CGCCTCGTCTCTAACT C AC139530.1 Ensembl:ENSG00000262049 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81701636..81701862 26863196 MeRIP-seq:(Medium) rs1568221250 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_820120,Human_RBP_ID_901706,Human_RBP_ID_5582619,Human_RBP_ID_8193514,Human_RBP_ID_13198615,Human_RBP_ID_22588958 100980 RMVar_ID_100980 Human_SNP_ID_634669736 m1A Human chr17 + 81702727 81702727 81702727 CGGGGGCCAGCGGGGCTGAAACGCGCCTCCTGAGTGTTGAAAGCGGCAGGCGCCGGCCTTTGCAC CGGGGGCCAGCGGGGCTGAAACGCGCCTCCTGGGTGTTGAAAGCGGCAGGCGCCGGCCTTTGCAC A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81702626..81702800 26863410 MeRIP-seq:(Medium) rs894122298 Functional Loss SNV dbSNP153 33..33 33 - - - 100981 RMVar_ID_100981 Human_SNP_ID_634669740 m1A Human chr17 + 81702742 81702742 81702742 CTGAAACGCGCCTCCTGAGTGTTGAAAGCGGCAGGCGCCGGCCTTTGCACCCAGAGGCCAGGGCG CTGAAACGCGCCTCCTGAGTGTTGAAAGCGGCCGGCGCCGGCCTTTGCACCCAGAGGCCAGGGCG A C HGS Ensembl:ENSG00000185359 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81702539..81702863;chr17:81702527..81703042;chr17:81702571..81702891 26863196 MeRIP-seq:(Medium) rs893605764 Functional Loss SNV dbSNP153 33..33 33 - - - 100982 RMVar_ID_100982 Human_SNP_ID_634669949 m1A Human chr17 - 81703243 81703243 81703243 GCAGCTAGACATCGGGCGACCCTCGTCCCGCCAGGTTTTGGGGTCGCGCAAACGAGCGACGGGGG GCAGCTAGACATCGGGCGACCCTCGTCCCGCCGGGTTTTGGGGTCGCGCAAACGAGCGACGGGGG T C AC139530.1 Ensembl:ENSG00000262049 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4467590 GWAS_ID_13199,GWAS_ID_13200,GWAS_ID_13201,GWAS_ID_13202,GWAS_ID_13203,GWAS_ID_13204,GWAS_ID_13205,GWAS_ID_13206,GWAS_ID_13207,GWAS_ID_13208,GWAS_ID_13209,GWAS_ID_13210,GWAS_ID_13211,GWAS_ID_13212,GWAS_ID_13213,GWAS_ID_13214,GWAS_ID_13215,GWAS_ID_13216,GWAS_ID_13217,GWAS_ID_13218,GWAS_ID_13219,GWAS_ID_13220,GWAS_ID_13221,GWAS_ID_13222,GWAS_ID_13223,GWAS_ID_13224,GWAS_ID_13225,GWAS_ID_13226 100983 RMVar_ID_100983 Human_SNP_ID_634670108 m1A Human chr17 + 81703574 81703574 81703574 TTGGGCTTCGGGCCGCTGCGTTCCGCCTTGCCAGGTACGCGGGATCCTGGGGCGGTCCGGGCCGG TTGGGCTTCGGGCCGCTGCGTTCCGCCTTGCCGGGTACGCGGGATCCTGGGGCGGTCCGGGCCGG A G MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81703526..81703575 26863196 MeRIP-seq:(Medium) rs767111957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464904,Human_RBP_ID_19080450,Human_RBP_ID_22445092,Human_RBP_ID_26782901,Human_RBP_ID_26812901,Human_RBP_ID_26974775 Human_Splice_Rec_1881671,Human_Splice_Rec_1881679 100984 RMVar_ID_100984 Human_SNP_ID_634670393 m1A Human chr17 + 81704333 81704333 81704333 GTGTGAGGCCCTCGCTGGTGCACCCCTGGATAACGCCCCCAAGGAGTACCCCCCCAAGATACAGC GTGTGAGGCCCTCGCTGGTGCACCCCTGGATAGCGCCCCCAAGGAGTACCCCCCCAAGATACAGC A G MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81704289..81704370 26863196 MeRIP-seq:(Medium) rs1405019309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51037,Human_RBP_ID_1185043,Human_RBP_ID_1544724,Human_RBP_ID_4459307,Human_RBP_ID_18439866,Human_RBP_ID_24532054 Human_Splice_Rec_1881672,Human_Splice_Rec_1881673,Human_Splice_Rec_1881680,Human_Splice_Rec_1881681 100985 RMVar_ID_100985 Human_SNP_ID_634671435 m1A Human chr17 + 81707253 81707253 81707253 GCACCGTGGTTCTGGAGTAGCCTCCAGCTCGGAGGACTTGTGTTCAGGGGTCCTGGGCCCCGGGC GCACCGTGGTTCTGGAGTAGCCTCCAGCTCGGTGGACTTGTGTTCAGGGGTCCTGGGCCCCGGGC A T MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr17:81707251..81707275;chr17:81707202..81707320 26863196 MeRIP-seq:(Medium) rs772984062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1544738,Human_RBP_ID_3951377,Human_RBP_ID_5115673,Human_RBP_ID_5368384,Human_RBP_ID_13198679,Human_RBP_ID_17654373,Human_RBP_ID_18711699,Human_RBP_ID_22223737,Human_RBP_ID_22443247,Human_RBP_ID_26974791,Human_RBP_ID_27262271 Human_miRNA_ID_2452822 RMVar_hsa_circ_120128,RMVar_hsa_circ_187752 100986 RMVar_ID_100986 Human_SNP_ID_634671439 m1A Human chr17 + 81707266 81707266 81707266 GGAGTAGCCTCCAGCTCGGAGGACTTGTGTTCAGGGGTCCTGGGCCCCGGGCGAGGTCCCGCCCT GGAGTAGCCTCCAGCTCGGAGGACTTGTGTTCGGGGGTCCTGGGCCCCGGGCGAGGTCCCGCCCT A G MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding 3'UTR,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1317726562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502682,Human_RBP_ID_1011070,Human_RBP_ID_1544738,Human_RBP_ID_3951377,Human_RBP_ID_5115673,Human_RBP_ID_5144484,Human_RBP_ID_5368384,Human_RBP_ID_8253812,Human_RBP_ID_13198679,Human_RBP_ID_17654373,Human_RBP_ID_18191043,Human_RBP_ID_22061801,Human_RBP_ID_22223737,Human_RBP_ID_22443247,Human_RBP_ID_23210549,Human_RBP_ID_26974791,Human_RBP_ID_27262271 Human_miRNA_ID_120245,Human_miRNA_ID_124060,Human_miRNA_ID_960055,Human_miRNA_ID_2452822 RMVar_hsa_circ_120128,RMVar_hsa_circ_187752 100987 RMVar_ID_100987 Human_SNP_ID_634672913 m1A Human chr17 + 81712103 81712103 81712103 GCGGTGGCCTTCGGCCCTGCGCTCCGGCCTGGAGAAGGGAGGACGCCAGGGGCCCGGGGGAGTGG GCGGTGGCCTTCGGCCCTGCGCTCCGGCCTGGGGAAGGGAGGACGCCAGGGGCCCGGGGGAGTGG A G AC139530.2 Ensembl:ENSG00000262660 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81712053..81712140 26863196 MeRIP-seq:(Medium) rs1313722203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120128,RMVar_hsa_circ_187752 100988 RMVar_ID_100988 Human_SNP_ID_634673074 m1A Human chr17 + 81712368 81712368 81712368 GGGCGCGGGGCGCGGGGCGCTGCGGCCGGTACACGCCGGGGTAGGGCCGGGGTCGGGTTGTGGTC GGGCGCGGGGCGCGGGGCGCTGCGGCCGGTACGCGCCGGGGTAGGGCCGGGGTCGGGTTGTGGTC A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81712304..81712475 26863196 MeRIP-seq:(Medium) rs1312501526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464909,Human_RBP_ID_5115783,Human_RBP_ID_8466181,Human_RBP_ID_9326970,Human_RBP_ID_13198942,Human_RBP_ID_17655009,Human_RBP_ID_18420327,Human_RBP_ID_27838629 RMVar_hsa_circ_120128,RMVar_hsa_circ_187752 100989 RMVar_ID_100989 Human_SNP_ID_634673087 m1A Human chr17 - 81712394 81712394 81712394 GGCCCAGGAGAGCCCAATCCCGGCCCGACCACAACCCGACCCCGGCCCTACCCCGGCGTGTACCG GGCCCAGGAGAGCCCAATCCCGGCCCGACCACGACCCGACCCCGGCCCTACCCCGGCGTGTACCG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:81712310..81712399 26863410 MeRIP-seq:(Medium) rs1448262036 Functional Loss SNV dbSNP153 33..33 33 - - - 100990 RMVar_ID_100990 Human_SNP_ID_634673091 m1A Human chr17 - 81712399 81712399 81712399 GCCATGGCCCAGGAGAGCCCAATCCCGGCCCGACCACAACCCGACCCCGGCCCTACCCCGGCGTG GCCATGGCCCAGGAGAGCCCAATCCCGGCCCGTCCACAACCCGACCCCGGCCCTACCCCGGCGTG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:81712303..81712434 26863410 MeRIP-seq:(Medium) rs944393718 Functional Loss SNV dbSNP153 33..33 33 - - - 100991 RMVar_ID_100991 Human_SNP_ID_634673128 m1A Human chr17 + 81712500 81712500 81712500 GCTGGCCTCCTGCGGGGCCGCCTGCTGCACGCACCCGCTGGACCTGCTCAAGGTGAGGCCGGGGC GCTGGCCTCCTGCGGGGCCGCCTGCTGCACGCCCCCGCTGGACCTGCTCAAGGTGAGGCCGGGGC A C SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81712433..81713275 32194978 MeRIP-seq:(Medium) rs1355059472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464910,Human_RBP_ID_5114944,Human_RBP_ID_5365323,Human_RBP_ID_13198948,Human_RBP_ID_18420327,Human_RBP_ID_19084475 Human_Splice_Rec_1881707,Human_Splice_Rec_1881727,Human_Splice_Rec_1881749,Human_Splice_Rec_1881769 RMVar_hsa_circ_120128,RMVar_hsa_circ_187752 100992 RMVar_ID_100992 Human_SNP_ID_634673938 m1A Human chr17 - 81715005 81715005 81715005 GTGCCAGGATGCCGTCGGTACGCACCACCCGCAGCGCCATGCCCGTCATGCGCAGCTTCACCTCC GTGCCAGGATGCCGTCGGTACGCACCACCCGCGGCGCCATGCCCGTCATGCGCAGCTTCACCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81714906..81715616 26863196 MeRIP-seq:(Medium) rs924283982 Functional Loss SNV dbSNP153 33..33 33 - - - 100993 RMVar_ID_100993 Human_SNP_ID_634675878 m1A Human chr17 + 81720077 81720077 81720077 CGCAAAAACTTTGGCATCAAAGTGCCATCCTGACCAGCCGTGGGAATGGCTGGGCTGCCAGGCCA CGCAAAAACTTTGGCATCAAAGTGCCATCCTGCCCAGCCGTGGGAATGGCTGGGCTGCCAGGCCA A C SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding CDS,stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81720026..81720967 32194978 MeRIP-seq:(Medium) rs763478303 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_502712,Human_RBP_ID_5115279,Human_RBP_ID_13199115,Human_RBP_ID_22445098,Human_RBP_ID_27262332 RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 100994 RMVar_ID_100994 Human_SNP_ID_634680346 m1A Human chr17 - 81734625 81734625 81734625 CCATCCTGTGGTCGGCCTGTCCTTCCAGGCTCAATCAGACGTCACCCCGCAGCCCTCCTGAGTCG CCATCCTGTGGTCGGCCTGTCCTTCCAGGCTCGATCAGACGTCACCCCGCAGCCCTCCTGAGTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81734577..81734693 26863196 MeRIP-seq:(Medium) rs1444943530 Functional Loss SNV dbSNP153 33..33 33 - - - 100995 RMVar_ID_100995 Human_SNP_ID_634682174 m1A Human chr17 - 81741277 81741277 81741277 GTCCTGGGCAGCGCCGGCGGGGAGGCAGGGGCACAGGGCAGGGAGGAGCAGCGCGATCCCTGGAT GTCCTGGGCAGCGCCGGCGGGGAGGCAGGGGCGCAGGGCAGGGAGGAGCAGCGCGATCCCTGGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81741267..81741338 26863196 MeRIP-seq:(Medium) rs1432911201 Functional Loss SNV dbSNP153 33..33 33 - - - 100996 RMVar_ID_100996 Human_SNP_ID_634683337 m1A Human chr17 + 81794146 81794142 81794146 ACAGAGACACACACAGATGCACATTGAGGCACACATAGACACACAAAAATACAGACACAGATGCA ACAGAGACACACACAGATGCACATTGAGG____CATAGACACACAAAAATACAGACACAGATGCA GCACA G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81793982..81794179 26863196 MeRIP-seq:(Medium) rs1329328000 Functional Loss DEL dbSNP153 30..33 33 - - - 100997 RMVar_ID_100997 Human_SNP_ID_634684779 m1A Human chr17 - 81801634 81801634 81801634 TGCCCGCAGCAAGATTCCTGTTATCTGGGTAGAGTCCTCAGCCTCCGCCACCCCCAGGCGATGTC TGCCCGCAGCAAGATTCCTGTTATCTGGGTAGGGTCCTCAGCCTCCGCCACCCCCAGGCGATGTC T C lnc-MCRIP1-1,lnc-MCRIP1-1:2 RNACentral:URS00008C3D98,RNACentral:URS00008C1A11 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81801626..81801711 26863196 MeRIP-seq:(Medium) rs1248322651 Functional Loss SNV dbSNP153 33..33 33 - - - 100998 RMVar_ID_100998 Human_SNP_ID_634685420 m1A Human chr17 - 81803964 81803955 81803964 CGCAGGGAGCGCCTCGTACCCCGGCCATACGCAGACTCGGCGCGCTGAATTCCACCCCGCGGACC CGCAGGGAGCGCCTCGTACCCCGGCCATACGC_________GCGCTGAATTCCACCCCGCGGACC CGCCGAGTCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81803913..81804044 26863196 MeRIP-seq:(Medium) rs1218656673 Functional Loss DEL dbSNP153 33..41 33 - - - 100999 RMVar_ID_100999 Human_SNP_ID_634687135 m1A Human chr17 - 81809261 81809250 81809262 AGACGGACAGGCAGACAGGCAGGCAGATGGATAGGCAGATGGACAGATGGACAGACAGACGGACA AGACGGACAGGCAGACAGGCAGGCAGATGGA____________CAGATGGACAGACAGACGGACA GTCCATCTGCCTA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81809223..81809721 26863196 MeRIP-seq:(Medium) rs1398081020 Functional Loss DEL dbSNP153 32..43 33 - - - 101000 RMVar_ID_101000 Human_SNP_ID_634687982 m1A Human chr17 + 81811105 81811105 81811105 GGCAGCCTTGGCGTGATGCCTCCCAGTGCCAGATGGATGGCGAGGAGATTGAGGTCCAGGTCAGT GGCAGCCTTGGCGTGATGCCTCCCAGTGCCAGGTGGATGGCGAGGAGATTGAGGTCCAGGTCAGT A G GCGR Ensembl:ENSG00000215644 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81811097..81811175 26863196 MeRIP-seq:(Medium) rs535086486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1881842,Human_Splice_Rec_1881843,Human_Splice_Rec_1881864,Human_Splice_Rec_1881865,Human_Splice_Rec_1881892 101001 RMVar_ID_101001 Human_SNP_ID_634692219 m1A Human chr17 - 81822816 81822816 81822816 TTTTGTCCTTGAAGTGGTCAGGATACAGGACAAGGGCAGCCCCACCCCATCCAGCCTGGGCTCCC TTTTGTCCTTGAAGTGGTCAGGATACAGGACAGGGGCAGCCCCACCCCATCCAGCCTGGGCTCCC T C MCRIP1 Ensembl:ENSG00000225663 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11550921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237190,Human_RBP_ID_502750,Human_RBP_ID_5115677,Human_RBP_ID_5143390,Human_RBP_ID_17654378,Human_RBP_ID_18513927,Human_RBP_ID_27458911 Human_Splice_Rec_1881904,Human_Splice_Rec_1881920,Human_Splice_Rec_1881932,Human_Splice_Rec_1881942 Human_miRNA_ID_1418975,Human_miRNA_ID_2255579,Human_miRNA_ID_2255580 RMVar_hsa_circ_82677,RMVar_hsa_circ_107045,RMVar_hsa_circ_122942,RMVar_hsa_circ_125951,RMVar_hsa_circ_117486,RMVar_hsa_circ_101199,RMVar_hsa_circ_187754,RMVar_hsa_circ_187756,RMVar_hsa_circ_187758,RMVar_hsa_circ_187759,RMVar_hsa_circ_187757,RMVar_hsa_circ_187755 101002 RMVar_ID_101002 Human_SNP_ID_634692758 m1A Human chr17 + 81824388 81824388 81824388 GGGGGCTGCTGGTCCTCTTGCCGTTGTACACGACTCTGGAGACGGGGGAGCTGGGGGAGCCTGGC GGGGGCTGCTGGTCCTCTTGCCGTTGTACACGGCTCTGGAGACGGGGGAGCTGGGGGAGCCTGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81824276..81824600 26863410 MeRIP-seq:(Medium) rs1234238140 Functional Loss SNV dbSNP153 33..33 33 - - - 101003 RMVar_ID_101003 Human_SNP_ID_634694559 m1A Human chr17 + 81829645 81829645 81829645 CTCAATGTACTGTAAAATATAGCGCAGCTCACAATGGCTGGGGTCTCACATGGGAGGACCCTCGA CTCAATGTACTGTAAAATATAGCGCAGCTCACCATGGCTGGGGTCTCACATGGGAGGACCCTCGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81829643..81829732 26863196 MeRIP-seq:(Medium) rs1321296653 Functional Loss SNV dbSNP153 33..33 33 - - - 101004 RMVar_ID_101004 Human_SNP_ID_634695280 m1A Human chr17 - 81832347 81832347 81832347 AGGGCGCACACGCTCAGGCTGTTGCTGCCACCACCCAGGGGAGAGGGTGAGGAGGTGGTGCAGCG AGGGCGCACACGCTCAGGCTGTTGCTGCCACCGCCCAGGGGAGAGGGTGAGGAGGTGGTGCAGCG T C MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81832344..81832504 26863196 MeRIP-seq:(Medium) rs1237816311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13199598 RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 101005 RMVar_ID_101005 Human_SNP_ID_634695551 m1A Human chr17 - 81833207 81833207 81833207 AGGTGAGGCGGGTGCGGCGCCGGGCGGCGGGGACGGGGCGGGGCGGGGCGGGCGCGGCTGGGCCC AGGTGAGGCGGGTGCGGCGCCGGGCGGCGGGGGCGGGGCGGGGCGGGGCGGGCGCGGCTGGGCCC T C MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81833187..81833275 26863196 MeRIP-seq:(Medium) rs961205019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3544236,Human_RBP_ID_8190571,Human_RBP_ID_19084495,Human_RBP_ID_26782912 RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 101006 RMVar_ID_101006 Human_SNP_ID_634698973 m1A Human chr17 + 81843927 81843927 81843927 CCTGGGTTTCCGGCGACGCCCTCCTTCAAGCGAGGCCGCAGGCTTCGGAGGCGTGCGCTGCTGCT CCTGGGTTTCCGGCGACGCCCTCCTTCAAGCGGGGCCGCAGGCTTCGGAGGCGTGCGCTGCTGCT A G AC145207.3 Ensembl:ENSG00000262831 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81843826..81844008 26863410 MeRIP-seq:(Medium) rs201016924 Functional Loss SNV dbSNP153 33..33 33 - - - 101007 RMVar_ID_101007 Human_SNP_ID_634699397 m1A Human chr17 - 81845156 81845156 81845156 AAATTCCTGGAGAGCGGTGGCCAGGATGGGGCAGGGGATGATGACGTGAGTGGGGTCACAGCCCT AAATTCCTGGAGAGCGGTGGCCAGGATGGGGCGGGGGATGATGACGTGAGTGGGGTCACAGCCCT T C P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81843851..81845250 32194978 MeRIP-seq:(Medium) rs1381947947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237043,Human_RBP_ID_820464,Human_RBP_ID_902043,Human_RBP_ID_6651950,Human_RBP_ID_8253817,Human_RBP_ID_17902925,Human_RBP_ID_22444018,Human_RBP_ID_22760995,Human_RBP_ID_22958333,Human_RBP_ID_23129876,Human_RBP_ID_23755120,Human_RBP_ID_26460039 Human_Splice_Rec_1882010,Human_Splice_Rec_1882011,Human_Splice_Rec_1882022,Human_Splice_Rec_1882023,Human_Splice_Rec_1882042,Human_Splice_Rec_1882043,Human_Splice_Rec_1882049,Human_Splice_Rec_1882052,Human_Splice_Rec_1882053,Human_Splice_Rec_1882060,Human_Splice_Rec_1882061,Human_Splice_Rec_1882078,Human_Splice_Rec_1882079,Human_Splice_Rec_1882086,Human_Splice_Rec_1882087 Human_miRNA_ID_2152168,Human_miRNA_ID_2420632 RMVar_hsa_circ_96174,RMVar_hsa_circ_118621,RMVar_hsa_circ_124594,RMVar_hsa_circ_187763,RMVar_hsa_circ_100494,RMVar_hsa_circ_104101,RMVar_hsa_circ_187765,RMVar_hsa_circ_95248,RMVar_hsa_circ_187764,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_187767,RMVar_hsa_circ_187768,RMVar_hsa_circ_187769 101008 RMVar_ID_101008 Human_SNP_ID_634700191 m1A Human chr17 - 81847328 81847328 81847328 TTTCTGTCCACAGTTTGATGAAGGCCGGAACAACTTTGAAGGGGAGGTCACCAAGGAGAACCTGC TTTCTGTCCACAGTTTGATGAAGGCCGGAACAGCTTTGAAGGGGAGGTCACCAAGGAGAACCTGC T C P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81847204..81847386 26863196 MeRIP-seq:(Medium) rs1398038074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502826,Human_RBP_ID_1544980,Human_RBP_ID_1870955,Human_RBP_ID_3539762,Human_RBP_ID_4459640,Human_RBP_ID_13199748,Human_RBP_ID_17902934,Human_RBP_ID_18191395,Human_RBP_ID_18711850,Human_RBP_ID_22445113,Human_RBP_ID_22761011,Human_RBP_ID_23129877,Human_RBP_ID_23755130 Human_Splice_Rec_1882000,Human_Splice_Rec_1882001,Human_Splice_Rec_1882013,Human_Splice_Rec_1882032,Human_Splice_Rec_1882033,Human_Splice_Rec_1882068,Human_Splice_Rec_1882069,Human_Splice_Rec_1882092,Human_Splice_Rec_1882093,Human_Splice_Rec_1882102,Human_Splice_Rec_1882103,Human_Splice_Rec_1882110,Human_Splice_Rec_1882111,Human_Splice_Rec_1882120,Human_Splice_Rec_1882121,Human_Splice_Rec_1882126,Human_Splice_Rec_1882127,Human_Splice_Rec_1882131,Human_Splice_Rec_1882138,Human_Splice_Rec_1882139,Human_Splice_Rec_1882146,Human_Splice_Rec_1882147,Human_Splice_Rec_1882152,Human_Splice_Rec_1882153,Human_Splice_Rec_1882162 Human_miRNA_ID_594118,Human_miRNA_ID_2567409 RMVar_hsa_circ_118621,RMVar_hsa_circ_187763,RMVar_hsa_circ_100494,RMVar_hsa_circ_104101,RMVar_hsa_circ_95248,RMVar_hsa_circ_187764,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_57811,RMVar_hsa_circ_187771,RMVar_hsa_circ_187769,RMVar_hsa_circ_338295,RMVar_hsa_circ_94283,RMVar_hsa_circ_362740,RMVar_hsa_circ_321931,RMVar_hsa_circ_84358,RMVar_hsa_circ_97360,RMVar_hsa_circ_187772,RMVar_hsa_circ_187773,RMVar_hsa_circ_375853,RMVar_hsa_circ_60678,RMVar_hsa_circ_187774,RMVar_hsa_circ_187775 101009 RMVar_ID_101009 Human_SNP_ID_634702643 m1A Human chr17 - 81855559 81855559 81855559 GTTAGCTGGCAGAGAGGCTGATGACATCGTGAACTGGCTGAAGAAGCGCACGGGCCCGGCTGCCA GTTAGCTGGCAGAGAGGCTGATGACATCGTGAGCTGGCTGAAGAAGCGCACGGGCCCGGCTGCCA T C P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81855508..81855626 26863196 MeRIP-seq:(Medium) rs1421847347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49554,Human_RBP_ID_820469,Human_RBP_ID_902053,Human_RBP_ID_1544988,Human_RBP_ID_5189193,Human_RBP_ID_5578009,Human_RBP_ID_8466311,Human_RBP_ID_13199887,Human_RBP_ID_17902937,Human_RBP_ID_18470183,Human_RBP_ID_22444039,Human_RBP_ID_22500772,Human_RBP_ID_22761021,Human_RBP_ID_23755138,Human_RBP_ID_26814150,Human_RBP_ID_27262399 Human_Splice_Rec_1881996,Human_Splice_Rec_1882028,Human_Splice_Rec_1882116,Human_Splice_Rec_1882134,Human_Splice_Rec_1882142,Human_Splice_Rec_1882166,Human_Splice_Rec_1882172,Human_Splice_Rec_1882178 RMVar_hsa_circ_118621,RMVar_hsa_circ_187763,RMVar_hsa_circ_100494,RMVar_hsa_circ_104101,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_57811,RMVar_hsa_circ_187771,RMVar_hsa_circ_187769,RMVar_hsa_circ_338295,RMVar_hsa_circ_94283,RMVar_hsa_circ_362740,RMVar_hsa_circ_84358,RMVar_hsa_circ_97360,RMVar_hsa_circ_187772,RMVar_hsa_circ_187773,RMVar_hsa_circ_187775,RMVar_hsa_circ_187776,RMVar_hsa_circ_271635,RMVar_hsa_circ_288418,RMVar_hsa_circ_187777,RMVar_hsa_circ_187778,RMVar_hsa_circ_107603 101010 RMVar_ID_101010 Human_SNP_ID_634703782 m1A Human chr17 - 81859252 81859252 81859252 CGCCACGGAGGAGTCTGACCTGGCCCAGCAGTACGGCGTGCGCGGCTATCCCACCATCAAGTTCT CGCCACGGAGGAGTCTGACCTGGCCCAGCAGTGCGGCGTGCGCGGCTATCCCACCATCAAGTTCT T C P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81859201..81859325 26863196 MeRIP-seq:(Medium) rs144034161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237052,Human_RBP_ID_502836,Human_RBP_ID_820470,Human_RBP_ID_902054,Human_RBP_ID_1545016,Human_RBP_ID_1870967,Human_RBP_ID_4459664,Human_RBP_ID_6652003,Human_RBP_ID_8466319,Human_RBP_ID_9258084,Human_RBP_ID_17262382,Human_RBP_ID_20282223,Human_RBP_ID_22444042,Human_RBP_ID_22761023,Human_RBP_ID_22807382,Human_RBP_ID_26974927,Human_RBP_ID_27262405,Human_RBP_ID_27458975 Human_Splice_Rec_1881995,Human_Splice_Rec_1882027,Human_Splice_Rec_1882065,Human_Splice_Rec_1882099,Human_Splice_Rec_1882125,Human_Splice_Rec_1882133,Human_Splice_Rec_1882151,Human_Splice_Rec_1882157,Human_Splice_Rec_1882164,Human_Splice_Rec_1882165,Human_Splice_Rec_1882171,Human_Splice_Rec_1882177 Human_miRNA_ID_1703093 RMVar_hsa_circ_118621,RMVar_hsa_circ_100494,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_57811,RMVar_hsa_circ_187769,RMVar_hsa_circ_94283,RMVar_hsa_circ_362740,RMVar_hsa_circ_187773,RMVar_hsa_circ_187776,RMVar_hsa_circ_288418,RMVar_hsa_circ_347461 101011 RMVar_ID_101011 Human_SNP_ID_634703795 m1A Human chr17 - 81859280 81859280 81859280 GTTCCGAGATCAGGTTGGCCAAGGTGGACGCCACGGAGGAGTCTGACCTGGCCCAGCAGTACGGC GTTCCGAGATCAGGTTGGCCAAGGTGGACGCCGCGGAGGAGTCTGACCTGGCCCAGCAGTACGGC T C P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81859143..81859432;chr17:81859186..81859354;chr17:81859179..81859321;chr17:81859229..81859443 26863196 MeRIP-seq:(Medium) rs775201620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502838,Human_RBP_ID_766572,Human_RBP_ID_820470,Human_RBP_ID_902054,Human_RBP_ID_1545017,Human_RBP_ID_1870969,Human_RBP_ID_3539771,Human_RBP_ID_4464916,Human_RBP_ID_6652005,Human_RBP_ID_8466319,Human_RBP_ID_9077021,Human_RBP_ID_9258084,Human_RBP_ID_13200027,Human_RBP_ID_18711873,Human_RBP_ID_22223887,Human_RBP_ID_22444042,Human_RBP_ID_22761024,Human_RBP_ID_22807382,Human_RBP_ID_23755147,Human_RBP_ID_26646576,Human_RBP_ID_26974927 Human_Splice_Rec_1881995,Human_Splice_Rec_1882027,Human_Splice_Rec_1882099,Human_Splice_Rec_1882125,Human_Splice_Rec_1882133,Human_Splice_Rec_1882157,Human_Splice_Rec_1882164,Human_Splice_Rec_1882165,Human_Splice_Rec_1882171,Human_Splice_Rec_1882177 Human_miRNA_ID_2027559,Human_miRNA_ID_2465179,Human_miRNA_ID_2663392,Human_miRNA_ID_2681845 RMVar_hsa_circ_118621,RMVar_hsa_circ_100494,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_57811,RMVar_hsa_circ_187769,RMVar_hsa_circ_94283,RMVar_hsa_circ_362740,RMVar_hsa_circ_187773,RMVar_hsa_circ_187776,RMVar_hsa_circ_288418,RMVar_hsa_circ_347461 101012 RMVar_ID_101012 Human_SNP_ID_634703821 m1A Human chr17 + 81859344 81859344 81859344 CCTTCTGCCTTCAGCTTCCCAGCGGCTTTGGCATACTCAGGGGCCAGAGCCTTGCAGTGGCCACA CCTTCTGCCTTCAGCTTCCCAGCGGCTTTGGCGTACTCAGGGGCCAGAGCCTTGCAGTGGCCACA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81859176..81859409 32194978 MeRIP-seq:(Medium) rs1186931217 Functional Loss SNV dbSNP153 33..33 33 - - - 101013 RMVar_ID_101013 Human_SNP_ID_634703830 m1A Human chr17 + 81859386 81859385 81859386 GCCAGAGCCTTGCAGTGGCCACACCAAGGGGCATCTGGAAGCGGAAATGAGATGCTAGAAAGCAG GCCAGAGCCTTGCAGTGGCCACACCAAGGGGC_TCTGGAAGCGGAAATGAGATGCTAGAAAGCAG CA C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:81859376..81859400 26863196 MeRIP-seq:(Medium) rs1325234633 Functional Loss DEL dbSNP153 33..33 33 - - - 101014 RMVar_ID_101014 Human_SNP_ID_634704204 m1A Human chr17 + 81860477 81860477 81860477 CAGGCACAGCAGAGCGCGGCGCAGCATGTCGGACACGGATCAGGCGGGGCGCTTCGGTTGGCGCC CAGGCACAGCAGAGCGCGGCGCAGCATGTCGGGCACGGATCAGGCGGGGCGCTTCGGTTGGCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81860269..81860575;chr17:81860248..81860575;chr17:81860225..81860525;chr17:81860326..81860575;chr17:81860376..81860526;chr17:81860326..81860625;chr17:81860295..81860575;chr17:81860264..81860575 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1205929315 Functional Loss SNV dbSNP153 33..33 33 - - - 101015 RMVar_ID_101015 Human_SNP_ID_634704211 m1A Human chr17 - 81860484 81860484 81860484 TCCCGGCGGCGCCAACCGAAGCGCCCCGCCTGATCCGTGTCCGACATGCTGCGCCGCGCTCTGCT TCCCGGCGGCGCCAACCGAAGCGCCCCGCCTGCTCCGTGTCCGACATGCTGCGCCGCGCTCTGCT T G P4HB Ensembl:ENSG00000185624 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81860370..81860550 26863196 MeRIP-seq:(Medium) rs1130664 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_132144,Human_RBP_ID_820473,Human_RBP_ID_902057,Human_RBP_ID_1545041,Human_RBP_ID_4459677,Human_RBP_ID_9326975,Human_RBP_ID_18711884,Human_RBP_ID_22444047,Human_RBP_ID_22532922,Human_RBP_ID_26456503,Human_RBP_ID_26974945,Human_RBP_ID_27458981 Human_miRNA_ID_1938345,Human_miRNA_ID_1949445 RMVar_hsa_circ_118621,RMVar_hsa_circ_100494,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_94283,RMVar_hsa_circ_187773 101016 RMVar_ID_101016 Human_SNP_ID_634704253 m1A Human chr17 + 81860531 81860531 81860531 CGGTTGGCGCCGCCGGGACAGCGGGGGCGACGAGAGCGCGCGCCGGTCCCGGCCTCGCCTTTATA CGGTTGGCGCCGCCGGGACAGCGGGGGCGACGGGAGCGCGCGCCGGTCCCGGCCTCGCCTTTATA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:81860430..81860544 26863410 MeRIP-seq:(Medium) rs1217588402 Functional Loss SNV dbSNP153 33..33 33 - - - 101017 RMVar_ID_101017 Human_SNP_ID_634704566 m1A Human chr17 + 81861182 81861182 81861182 CCGCCTAGGGTCGGCGGTGGGCTCGGTGTGGGATAGCCGGCCCGGTCCGACGCGCTCCGCGAGGT CCGCCTAGGGTCGGCGGTGGGCTCGGTGTGGGCTAGCCGGCCCGGTCCGACGCGCTCCGCGAGGT A C lnc-ANAPC11-7,lnc-ANAPC11-7:2,lnc-ANAPC11-7:3 RNACentral:URS00008B4FDE,RNACentral:URS0000D58631,RNACentral:URS0000D57225 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81861142..81861300 26863196 MeRIP-seq:(Medium) rs1475686741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26974946 101018 RMVar_ID_101018 Human_SNP_ID_634704607 m1A Human chr17 - 81861314 81861314 81861314 CCGCCCGTCTCTCCAGCCCCATTCTCCTAACCACCCGCCCTGTGCTCGTATCCCCTCCGAGGCTT CCGCCCGTCTCTCCAGCCCCATTCTCCTAACCGCCCGCCCTGTGCTCGTATCCCCTCCGAGGCTT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81861202..81861331 26863196 MeRIP-seq:(Medium) rs1349448320 Functional Loss SNV dbSNP153 33..33 33 - - - 101019 RMVar_ID_101019 Human_SNP_ID_634704851 m1A Human chr17 + 81862078 81862078 81862078 AAAAAAAAAAAAAGTGTGCGTGTAGGGGCTGGAGGACAGAAGGTACAGTATTTCGTTAATAACTT AAAAAAAAAAAAAGTGTGCGTGTAGGGGCTGGCGGACAGAAGGTACAGTATTTCGTTAATAACTT A C lnc-ANAPC11-7,lnc-ANAPC11-7:2,lnc-ANAPC11-7:3 RNACentral:URS00008B4FDE,RNACentral:URS0000D58631,RNACentral:URS0000D57225 lincRNA,lincRNA,lincRNA exon,exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2889406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10483484,Human_RBP_ID_23755161,Human_RBP_ID_26456505 101020 RMVar_ID_101020 Human_SNP_ID_634704852 m1A Human chr17 + 81862078 81862078 81862078 AAAAAAAAAAAAAGTGTGCGTGTAGGGGCTGGAGGACAGAAGGTACAGTATTTCGTTAATAACTT AAAAAAAAAAAAAGTGTGCGTGTAGGGGCTGGGGGACAGAAGGTACAGTATTTCGTTAATAACTT A G lnc-ANAPC11-7,lnc-ANAPC11-7:2,lnc-ANAPC11-7:3 RNACentral:URS00008B4FDE,RNACentral:URS0000D58631,RNACentral:URS0000D57225 lincRNA,lincRNA,lincRNA exon,exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2889406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10483484,Human_RBP_ID_23755161,Human_RBP_ID_26456505 101021 RMVar_ID_101021 Human_SNP_ID_634706708 m1A Human chr17 - 81868230 81868230 81868230 GGGACACGTGGGGTGTGCTGCTGCTGCTCCCCAGCCCACCAGTGCCTGGCCAGCCTGCCCCCTTC GGGACACGTGGGGTGTGCTGCTGCTGCTCCCCGGCCCACCAGTGCCTGGCCAGCCTGCCCCCTTC T C ARHGDIA Ensembl:ENSG00000141522 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81868216..81868371 26863196 MeRIP-seq:(Medium) rs1339280299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131385,Human_RBP_ID_502872,Human_RBP_ID_1289564,Human_RBP_ID_4480865,Human_RBP_ID_6652095,Human_RBP_ID_17902960,Human_RBP_ID_21975857,Human_RBP_ID_23755185,Human_RBP_ID_26458466 Human_miRNA_ID_842764,Human_miRNA_ID_1357694,Human_miRNA_ID_2368127,Human_miRNA_ID_2368128,Human_miRNA_ID_2685949,Human_miRNA_ID_2685950,Human_miRNA_ID_2874082,Human_miRNA_ID_2874083,Human_miRNA_ID_2982044,Human_miRNA_ID_2982045,Human_miRNA_ID_3015913,Human_miRNA_ID_3015914 RMVar_hsa_circ_113234,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187780,RMVar_hsa_circ_187782,RMVar_hsa_circ_82273,RMVar_hsa_circ_187781,RMVar_hsa_circ_187779 101022 RMVar_ID_101022 Human_SNP_ID_634706863 m1A Human chr17 + 81868497 81868495 81868497 ACACCCCAGCTCCACCCCGGAGCAGCAGACGCACACGTCCAGGGGCAACCACGGGGCCTGGAGAA ACACCCCAGCTCCACCCCGGAGCAGCAGACG__CACGTCCAGGGGCAACCACGGGGCCTGGAGAA GCA G AC145207.2 Ensembl:ENSG00000262413 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81868476..81868500 26863196 MeRIP-seq:(Medium) rs1567849121 Functional Loss DEL dbSNP153 32..33 33 - - - 101023 RMVar_ID_101023 Human_SNP_ID_634706867 m1A Human chr17 + 81868497 81868497 81868497 ACACCCCAGCTCCACCCCGGAGCAGCAGACGCACACGTCCAGGGGCAACCACGGGGCCTGGAGAA ACACCCCAGCTCCACCCCGGAGCAGCAGACGCGCACGTCCAGGGGCAACCACGGGGCCTGGAGAA A G AC145207.2 Ensembl:ENSG00000262413 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81868476..81868500 26863196 MeRIP-seq:(Medium) rs1170559998 Functional Loss SNV dbSNP153 33..33 33 - - - 101024 RMVar_ID_101024 Human_SNP_ID_634706888 m1A Human chr17 - 81868537 81868537 81868537 CACACCCGAGGCCTGGCTTCAGGAGGGAGCGGAGCAGCCATTCTCCAGGCCCCGTGGTTGCCCCT CACACCCGAGGCCTGGCTTCAGGAGGGAGCGGGGCAGCCATTCTCCAGGCCCCGTGGTTGCCCCT T C ARHGDIA Ensembl:ENSG00000141522 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81868501..81868925 26863196 MeRIP-seq:(Medium) rs964875144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48536,Human_RBP_ID_236362,Human_RBP_ID_502879,Human_RBP_ID_820907,Human_RBP_ID_1011102,Human_RBP_ID_1370249,Human_RBP_ID_1870995,Human_RBP_ID_5114955,Human_RBP_ID_5143393,Human_RBP_ID_6652101,Human_RBP_ID_8191530,Human_RBP_ID_9327559,Human_RBP_ID_17080359,Human_RBP_ID_17262395,Human_RBP_ID_17902965,Human_RBP_ID_18942433,Human_RBP_ID_26456550 Human_Splice_Rec_1882216,Human_Splice_Rec_1882246 RMVar_hsa_circ_113234,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187780,RMVar_hsa_circ_187782,RMVar_hsa_circ_82273,RMVar_hsa_circ_187781,RMVar_hsa_circ_187779 101025 RMVar_ID_101025 Human_SNP_ID_634706944 m1A Human chr17 - 81868630 81868630 81868630 TCTCGTTGCTGCTTCTGCCTGTGCTGTGGGGGAGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTT TCTCGTTGCTGCTTCTGCCTGTGCTGTGGGGGGGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTT T C ARHGDIA Ensembl:ENSG00000141522 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81868583..81868789 26863196 MeRIP-seq:(Medium) rs780000070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236363,Human_RBP_ID_502884,Human_RBP_ID_765521,Human_RBP_ID_1545130,Human_RBP_ID_5114956,Human_RBP_ID_5129796,Human_RBP_ID_6652103,Human_RBP_ID_17494544,Human_RBP_ID_17654392,Human_RBP_ID_17902969,Human_RBP_ID_18942433,Human_RBP_ID_23755192,Human_RBP_ID_26458471,Human_RBP_ID_26974984,Human_RBP_ID_27459014 Human_Splice_Rec_1882183 Human_miRNA_ID_2333102,Human_miRNA_ID_2333103,Human_miRNA_ID_2966184,Human_miRNA_ID_2966185 RMVar_hsa_circ_113234,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187780,RMVar_hsa_circ_187782,RMVar_hsa_circ_82273,RMVar_hsa_circ_187781,RMVar_hsa_circ_187779 101026 RMVar_ID_101026 Human_SNP_ID_634706945 m1A Human chr17 - 81868630 81868630 81868630 TCTCGTTGCTGCTTCTGCCTGTGCTGTGGGGGAGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTT TCTCGTTGCTGCTTCTGCCTGTGCTGTGGGGGCGAGAGGCCGCAGCCAGGCCTCTGCTGCCCTTT T G ARHGDIA Ensembl:ENSG00000141522 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81868583..81868789 26863196 MeRIP-seq:(Medium) rs780000070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236363,Human_RBP_ID_502884,Human_RBP_ID_765521,Human_RBP_ID_1545130,Human_RBP_ID_5114956,Human_RBP_ID_5129796,Human_RBP_ID_6652103,Human_RBP_ID_17494544,Human_RBP_ID_17654392,Human_RBP_ID_17902969,Human_RBP_ID_18942433,Human_RBP_ID_23755192,Human_RBP_ID_26458471,Human_RBP_ID_26974984,Human_RBP_ID_27459014 Human_Splice_Rec_1882183 Human_miRNA_ID_2333102,Human_miRNA_ID_2333103,Human_miRNA_ID_2966184,Human_miRNA_ID_2966185 RMVar_hsa_circ_113234,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187780,RMVar_hsa_circ_187782,RMVar_hsa_circ_82273,RMVar_hsa_circ_187781,RMVar_hsa_circ_187779 101027 RMVar_ID_101027 Human_SNP_ID_634706999 m1A Human chr17 + 81868705 81868703 81868706 AGGAGGCTGGGCCTGTGGGTGGGGGAGGGCTGAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCAG AGGAGGCTGGGCCTGTGGGTGGGGGAGGGCT___GAGGGGGGTCGGAGGCACTCGGTTGAGCCAG TGAG T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr17:81868605..81868887;chr17:81868603..81868780 26863410 MeRIP-seq:(Medium) rs1422404073 Functional Loss DEL dbSNP153 32..34 33 - - - 101028 RMVar_ID_101028 Human_SNP_ID_634707004 m1A Human chr17 + 81868708 81868708 81868708 AGGCTGGGCCTGTGGGTGGGGGAGGGCTGAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCAGGCC AGGCTGGGCCTGTGGGTGGGGGAGGGCTGAGGGGGGGGGTCGGAGGCACTCGGTTGAGCCAGGCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81868606..81869025 26863410 MeRIP-seq:(Medium) rs754414636 Functional Loss SNV dbSNP153 33..33 33 - - - 101029 RMVar_ID_101029 Human_SNP_ID_634707029 m1A Human chr17 + 81868736 81868736 81868736 GAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCAGGCCAGGGAGGCGGACCAGGGTGGGAGGGGCA GAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCCGGCCAGGGAGGCGGACCAGGGTGGGAGGGGCA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81868551..81868950 26863196 MeRIP-seq:(Medium) rs1230807206 Functional Loss SNV dbSNP153 33..33 33 - - - 101030 RMVar_ID_101030 Human_SNP_ID_634707030 m1A Human chr17 + 81868736 81868736 81868736 GAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCAGGCCAGGGAGGCGGACCAGGGTGGGAGGGGCA GAGGAGGGGGGTCGGAGGCACTCGGTTGAGCCGGGCCAGGGAGGCGGACCAGGGTGGGAGGGGCA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81868551..81868950 26863196 MeRIP-seq:(Medium) rs1230807206 Functional Loss SNV dbSNP153 33..33 33 - - - 101031 RMVar_ID_101031 Human_SNP_ID_634707059 m1A Human chr17 + 81868785 81868785 81868785 CAGGGTGGGAGGGGCACGGAGGGCCTGTCAGCACTTTGGTATGGGGAGGGGAGGGGCTGGGGGGG CAGGGTGGGAGGGGCACGGAGGGCCTGTCAGCCCTTTGGTATGGGGAGGGGAGGGGCTGGGGGGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:81868548..81868976 26863196 MeRIP-seq:(Medium) rs1300757975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17902970 101032 RMVar_ID_101032 Human_SNP_ID_634707226 m1A Human chr17 + 81869044 81869044 81869044 GTCAGGAACTCGTACTCCTCGGCCCGGGGCCCATAGCTGCCTACCATGTAGTCAGTCTTGTCAAC GTCAGGAACTCGTACTCCTCGGCCCGGGGCCCGTAGCTGCCTACCATGTAGTCAGTCTTGTCAAC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81869026..81869050 26863196 MeRIP-seq:(Medium) rs1452644513 Functional Loss SNV dbSNP153 33..33 33 - - - 101033 RMVar_ID_101033 Human_SNP_ID_634707414 m1A Human chr17 + 81869400 81869400 81869400 TCAGCACAAACGACTGCTTCTTGAAGCTCTCCAGGTCGCCTGTTGGGGGGACCTCCCCCTCAATG TCAGCACAAACGACTGCTTCTTGAAGCTCTCCTGGTCGCCTGTTGGGGGGACCTCCCCCTCAATG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81869351..81869624;chr17:81869351..81869634;chr17:81869351..81869575 26863196 MeRIP-seq:(Medium) rs1293082990 Functional Loss SNV dbSNP153 33..33 33 - - - 101034 RMVar_ID_101034 Human_SNP_ID_634707516 m1A Human chr17 + 81869531 81869531 81869531 CCACCAGGGGCCGCCCGGACCCCCGCGGCCGCAGGGCACTCACCCGTCAGGTCCAGCTCCAGGGG CCACCAGGGGCCGCCCGGACCCCCGCGGCCGCCGGGCACTCACCCGTCAGGTCCAGCTCCAGGGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81869526..81869600 26863196 MeRIP-seq:(Medium) rs767269457 Functional Loss SNV dbSNP153 33..33 33 - - - 101035 RMVar_ID_101035 Human_SNP_ID_634707517 m1A Human chr17 + 81869531 81869531 81869531 CCACCAGGGGCCGCCCGGACCCCCGCGGCCGCAGGGCACTCACCCGTCAGGTCCAGCTCCAGGGG CCACCAGGGGCCGCCCGGACCCCCGCGGCCGCTGGGCACTCACCCGTCAGGTCCAGCTCCAGGGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81869526..81869600 26863196 MeRIP-seq:(Medium) rs767269457 Functional Loss SNV dbSNP153 33..33 33 - - - 101036 RMVar_ID_101036 Human_SNP_ID_634707720 m1A Human chr17 - 81869893 81869893 81869893 TGAGCAGGAGCCCACAGCCGAGCAGCTGGCCCAGATTGCAGCGGAGAACGAGGAGGATGAGCACT TGAGCAGGAGCCCACAGCCGAGCAGCTGGCCCGGATTGCAGCGGAGAACGAGGAGGATGAGCACT T C ARHGDIA Ensembl:ENSG00000141522 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:81869793..81869982 26863196 MeRIP-seq:(Medium) rs1204802296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502905,Human_RBP_ID_1545151,Human_RBP_ID_1871003,Human_RBP_ID_4459777,Human_RBP_ID_5114957,Human_RBP_ID_8466386,Human_RBP_ID_9377104,Human_RBP_ID_13200281 Human_Splice_Rec_1882186,Human_Splice_Rec_1882196,Human_Splice_Rec_1882206,Human_Splice_Rec_1882218,Human_Splice_Rec_1882236,Human_Splice_Rec_1882248,Human_Splice_Rec_1882252,Human_Splice_Rec_1882264,Human_Splice_Rec_1882272,Human_Splice_Rec_1882282,Human_Splice_Rec_1882290,Human_Splice_Rec_1882296,Human_Splice_Rec_1882300 Human_miRNA_ID_2663396,Human_miRNA_ID_2663397,Human_miRNA_ID_2681849,Human_miRNA_ID_2681850 RMVar_hsa_circ_56270,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187782,RMVar_hsa_circ_187781 101037 RMVar_ID_101037 Human_SNP_ID_634707741 m1A Human chr17 - 81869930 81869930 81869930 CACAGGTGTCCCGACCCAGGCTAAGCTTGAGCATGGCTGAGCAGGAGCCCACAGCCGAGCAGCTG CACAGGTGTCCCGACCCAGGCTAAGCTTGAGCCTGGCTGAGCAGGAGCCCACAGCCGAGCAGCTG T G ARHGDIA Ensembl:ENSG00000141522 Protein coding start codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81869532..81870024 32194978 MeRIP-seq:(Medium) rs767705875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502906,Human_RBP_ID_1185107,Human_RBP_ID_1545151,Human_RBP_ID_1871006,Human_RBP_ID_4459779,Human_RBP_ID_9377105,Human_RBP_ID_18420533,Human_RBP_ID_18711927,Human_RBP_ID_26330922,Human_RBP_ID_26975004 Human_Splice_Rec_1882186,Human_Splice_Rec_1882196,Human_Splice_Rec_1882206,Human_Splice_Rec_1882218,Human_Splice_Rec_1882236,Human_Splice_Rec_1882248,Human_Splice_Rec_1882252,Human_Splice_Rec_1882264,Human_Splice_Rec_1882272,Human_Splice_Rec_1882282,Human_Splice_Rec_1882290,Human_Splice_Rec_1882296,Human_Splice_Rec_1882300 RMVar_hsa_circ_56270,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187782,RMVar_hsa_circ_187781 101038 RMVar_ID_101038 Human_SNP_ID_634707744 m1A Human chr17 - 81869939 81869939 81869939 CGTCCCGCCCACAGGTGTCCCGACCCAGGCTAAGCTTGAGCATGGCTGAGCAGGAGCCCACAGCC CGTCCCGCCCACAGGTGTCCCGACCCAGGCTATGCTTGAGCATGGCTGAGCAGGAGCCCACAGCC T A ARHGDIA Ensembl:ENSG00000141522 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:81869876..81870000 26863410 MeRIP-seq:(Medium) rs1427492584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502906,Human_RBP_ID_898903,Human_RBP_ID_1545151,Human_RBP_ID_1871006,Human_RBP_ID_4459779,Human_RBP_ID_9327560,Human_RBP_ID_9377105,Human_RBP_ID_18420533,Human_RBP_ID_19080481,Human_RBP_ID_26330922,Human_RBP_ID_26975004 Human_Splice_Rec_1882186,Human_Splice_Rec_1882196,Human_Splice_Rec_1882206,Human_Splice_Rec_1882218,Human_Splice_Rec_1882236,Human_Splice_Rec_1882248,Human_Splice_Rec_1882252,Human_Splice_Rec_1882264,Human_Splice_Rec_1882272,Human_Splice_Rec_1882282,Human_Splice_Rec_1882290,Human_Splice_Rec_1882296,Human_Splice_Rec_1882300 RMVar_hsa_circ_56270,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187782,RMVar_hsa_circ_187781 101039 RMVar_ID_101039 Human_SNP_ID_634707745 m1A Human chr17 - 81869940 81869940 81869940 CCGTCCCGCCCACAGGTGTCCCGACCCAGGCTAAGCTTGAGCATGGCTGAGCAGGAGCCCACAGC CCGTCCCGCCCACAGGTGTCCCGACCCAGGCTGAGCTTGAGCATGGCTGAGCAGGAGCCCACAGC T C ARHGDIA Ensembl:ENSG00000141522 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:81869901..81869975;chr17:81869826..81869975 26863196 MeRIP-seq:(Medium) rs1051220905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502906,Human_RBP_ID_898903,Human_RBP_ID_1545151,Human_RBP_ID_4459779,Human_RBP_ID_9327560,Human_RBP_ID_18420533,Human_RBP_ID_19080481,Human_RBP_ID_26330922,Human_RBP_ID_26975004 Human_Splice_Rec_1882186,Human_Splice_Rec_1882196,Human_Splice_Rec_1882206,Human_Splice_Rec_1882218,Human_Splice_Rec_1882236,Human_Splice_Rec_1882248,Human_Splice_Rec_1882252,Human_Splice_Rec_1882264,Human_Splice_Rec_1882272,Human_Splice_Rec_1882282,Human_Splice_Rec_1882290,Human_Splice_Rec_1882296,Human_Splice_Rec_1882300 RMVar_hsa_circ_56270,RMVar_hsa_circ_92085,RMVar_hsa_circ_92548,RMVar_hsa_circ_187782,RMVar_hsa_circ_187781 101040 RMVar_ID_101040 Human_SNP_ID_634707973 m1A Human chr17 - 81870606 81870606 81870606 CGGGTCAGTGCTGCCCCGGGCACTCCGGGCCCACCATCTACAAGAGGGCCCGAGAGTACTGAGTG CGGGTCAGTGCTGCCCCGGGCACTCCGGGCCCGCCATCTACAAGAGGGCCCGAGAGTACTGAGTG T C ARHGDIA Ensembl:ENSG00000141522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81870605..81871375 26863196 MeRIP-seq:(Medium) rs1344745513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084515 RMVar_hsa_circ_92548,RMVar_hsa_circ_187782 101041 RMVar_ID_101041 Human_SNP_ID_634707977 m1A Human chr17 - 81870617 81870617 81870617 AGATCCCCTGCCGGGTCAGTGCTGCCCCGGGCACTCCGGGCCCACCATCTACAAGAGGGCCCGAG AGATCCCCTGCCGGGTCAGTGCTGCCCCGGGCCCTCCGGGCCCACCATCTACAAGAGGGCCCGAG T G ARHGDIA Ensembl:ENSG00000141522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81870615..81870805 26863196 MeRIP-seq:(Medium) rs968786283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084515 RMVar_hsa_circ_92548,RMVar_hsa_circ_187782 101042 RMVar_ID_101042 Human_SNP_ID_634708200 m1A Human chr17 + 81871205 81871205 81871205 AGGGCGGGGCGCGAACAAAGGCGGAAGCCCCCACCTCAGCGCCCCCCGCCCCCGCCGGCGCCGCC AGGGCGGGGCGCGAACAAAGGCGGAAGCCCCCCCCTCAGCGCCCCCCGCCCCCGCCGGCGCCGCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81871185..81871350 26863196 MeRIP-seq:(Medium) rs1344858450 Functional Loss SNV dbSNP153 33..33 33 - - - 101043 RMVar_ID_101043 Human_SNP_ID_634708229 m1A Human chr17 - 81871240 81871240 81871240 CGGCGGGGCGGAGGCGGCGGGTCGGGGCGGGGACCGGCGGCGCCGGCGGGGGCGGGGGGCGCTGA CGGCGGGGCGGAGGCGGCGGGTCGGGGCGGGGGCCGGCGGCGCCGGCGGGGGCGGGGGGCGCTGA T C ARHGDIA Ensembl:ENSG00000141522 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:81871235..81871350;chr17:81871229..81871375 26863410 MeRIP-seq:(Medium) rs980183083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190579,Human_RBP_ID_19084518,Human_RBP_ID_26782921 RMVar_hsa_circ_92548,RMVar_hsa_circ_187782 101044 RMVar_ID_101044 Human_SNP_ID_634712964 m1A Human chr17 + 81885794 81885794 81885794 GCTGGTGCCTCTGCCCAGCCTGTCCAATGCTGACGCCCCTCAGCTGGCTCCTTCCTGGGGCCTTC GCTGGTGCCTCTGCCCAGCCTGTCCAATGCTGCCGCCCCTCAGCTGGCTCCTTCCTGGGGCCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81885746..81885935 26863196 MeRIP-seq:(Medium) rs1407911097 Functional Loss SNV dbSNP153 33..33 33 - - - 101045 RMVar_ID_101045 Human_SNP_ID_634712972 m1A Human chr17 - 81885827 81885827 81885827 TTGGGGAACTGGGTGGGTAGGTGTCACTGGAGAGAAGGCCCCAGGAAGGAGCCAGCTGAGGGGCG TTGGGGAACTGGGTGGGTAGGTGTCACTGGAGTGAAGGCCCCAGGAAGGAGCCAGCTGAGGGGCG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81885731..81885924 26863196 MeRIP-seq:(Medium) rs1012392632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011141,Human_RBP_ID_6652473,Human_RBP_ID_17903079,Human_RBP_ID_23755254,Human_RBP_ID_26456600 101046 RMVar_ID_101046 Human_SNP_ID_634712973 m1A Human chr17 - 81885827 81885827 81885827 TTGGGGAACTGGGTGGGTAGGTGTCACTGGAGAGAAGGCCCCAGGAAGGAGCCAGCTGAGGGGCG TTGGGGAACTGGGTGGGTAGGTGTCACTGGAGGGAAGGCCCCAGGAAGGAGCCAGCTGAGGGGCG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81885731..81885924 26863196 MeRIP-seq:(Medium) rs1012392632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011141,Human_RBP_ID_6652473,Human_RBP_ID_17903079,Human_RBP_ID_23755254,Human_RBP_ID_26456600 101047 RMVar_ID_101047 Human_SNP_ID_634713867 m1A Human chr17 - 81888351 81888339 81888351 CTGGAGGTTTTGGTGGTGGTGGAGGCACCCGGAGAGGCACCCGCGGAGGCGCCCGTGGAAGAGGC CTGGAGGTTTTGGTGGTGGTGGAGGCACCCGG____________GGAGGCGCCCGTGGAAGAGGC CGCGGGTGCCTCT C ALYREF Ensembl:ENSG00000183684 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81888226..81888407 26863196 MeRIP-seq:(Medium) rs1302765190 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_237005,Human_RBP_ID_302012,Human_RBP_ID_503019,Human_RBP_ID_764117,Human_RBP_ID_821718,Human_RBP_ID_4460083,Human_RBP_ID_5365354,Human_RBP_ID_6652572,Human_RBP_ID_8823600,Human_RBP_ID_22061810,Human_RBP_ID_26332585,Human_RBP_ID_27262490 Human_Splice_Rec_1882312,Human_Splice_Rec_1882318 RMVar_hsa_circ_187783,RMVar_hsa_circ_117321,RMVar_hsa_circ_56804 101048 RMVar_ID_101048 Human_SNP_ID_634713870 m1A Human chr17 - 81888351 81888340 81888352 CTGGAGGTTTTGGTGGTGGTGGAGGCACCCGGAGAGGCACCCGCGGAGGCGCCCGTGGAAGAGGC CTGGAGGTTTTGGTGGTGGTGGAGGCACCCG____________CGGAGGCGCCCGTGGAAGAGGC GCGGGTGCCTCTC G ALYREF Ensembl:ENSG00000183684 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81888226..81888407 26863196 MeRIP-seq:(Medium) rs768732986 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_237005,Human_RBP_ID_302012,Human_RBP_ID_503019,Human_RBP_ID_764117,Human_RBP_ID_821718,Human_RBP_ID_4460083,Human_RBP_ID_5365354,Human_RBP_ID_6652572,Human_RBP_ID_8823600,Human_RBP_ID_22061810,Human_RBP_ID_26332585,Human_RBP_ID_27262490 Human_Splice_Rec_1882312,Human_Splice_Rec_1882318 RMVar_hsa_circ_187783,RMVar_hsa_circ_117321,RMVar_hsa_circ_56804 101049 RMVar_ID_101049 Human_SNP_ID_634713884 m1A Human chr17 - 81888361 81888361 81888361 AACCGTGGCGCTGGAGGTTTTGGTGGTGGTGGAGGCACCCGGAGAGGCACCCGCGGAGGCGCCCG AACCGTGGCGCTGGAGGTTTTGGTGGTGGTGGCGGCACCCGGAGAGGCACCCGCGGAGGCGCCCG T G ALYREF Ensembl:ENSG00000183684 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs749533457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49486,Human_RBP_ID_302012,Human_RBP_ID_764117,Human_RBP_ID_821718,Human_RBP_ID_4460083,Human_RBP_ID_5365354,Human_RBP_ID_6652572,Human_RBP_ID_8823600,Human_RBP_ID_13200821,Human_RBP_ID_22061810,Human_RBP_ID_23129885,Human_RBP_ID_23755280,Human_RBP_ID_26332585,Human_RBP_ID_27262490 Human_Splice_Rec_1882312,Human_Splice_Rec_1882318 RMVar_hsa_circ_187783,RMVar_hsa_circ_117321,RMVar_hsa_circ_56804 101050 RMVar_ID_101050 Human_SNP_ID_634714819 m1A Human chr17 - 81890916 81890916 81890916 CGCTGGCGGCCCCGTTTCGGCCGGATCCTCTCAGGCCGGGAAGAGGAAGGGTCCGGAGTAGCCGT CGCTGGCGGCCCCGTTTCGGCCGGATCCTCTCGGGCCGGGAAGAGGAAGGGTCCGGAGTAGCCGT T C ALYREF Ensembl:ENSG00000183684 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81890914..81891030 26863196 MeRIP-seq:(Medium) rs1377235214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362238 101051 RMVar_ID_101051 Human_SNP_ID_634715006 m1A Human chr17 - 81891312 81891312 81891312 CCGACCGGCGCCCTACAGCAGGGTGAGTGCGGAGGCCGGCCGCGCCGGAGAGTGGGAGGGGGCCA CCGACCGGCGCCCTACAGCAGGGTGAGTGCGGGGGCCGGCCGCGCCGGAGAGTGGGAGGGGGCCA T C ALYREF Ensembl:ENSG00000183684 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81891301..81891450 32194978 MeRIP-seq:(Medium) rs1374836235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084529 101052 RMVar_ID_101052 Human_SNP_ID_634715045 m1A Human chr17 - 81891415 81891415 81891415 GCGGCGGTGGGGCGCAGGCCGCCGCGCGAGTGAATCGAGGCGGCGGGCCCATCCGGAACCGGCCG GCGGCGGTGGGGCGCAGGCCGCCGCGCGAGTGTATCGAGGCGGCGGGCCCATCCGGAACCGGCCG T A ALYREF Ensembl:ENSG00000183684 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:81891301..81891575 26863410 MeRIP-seq:(Medium) rs1472199148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767530,Human_RBP_ID_4460120,Human_RBP_ID_6652607,Human_RBP_ID_13200881,Human_RBP_ID_17126841,Human_RBP_ID_17903126,Human_RBP_ID_18711966,Human_RBP_ID_22444052 Human_Splice_Rec_1882305,Human_Splice_Rec_1882319 101053 RMVar_ID_101053 Human_SNP_ID_634715267 m1A Human chr17 - 81891786 81891786 81891786 CAGCGCCGGCGTCCGCGCGGGAAGGTATAAAAACGACCACAGTCGCGGCCCGACTCCCTCAACAG CAGCGCCGGCGTCCGCGCGGGAAGGTATAAAACCGACCACAGTCGCGGCCCGACTCCCTCAACAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81891678..81893110;chr17:81891683..81893625 26863196 MeRIP-seq:(Medium) rs1156601335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4460128 101054 RMVar_ID_101054 Human_SNP_ID_634715268 m1A Human chr17 - 81891787 81891787 81891787 GCAGCGCCGGCGTCCGCGCGGGAAGGTATAAAAACGACCACAGTCGCGGCCCGACTCCCTCAACA GCAGCGCCGGCGTCCGCGCGGGAAGGTATAAACACGACCACAGTCGCGGCCCGACTCCCTCAACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:81891683..81893110;chr17:81891676..81893110 26863196 MeRIP-seq:(Medium) rs1308751409 Functional Loss SNV dbSNP153 33..33 33 - - - 101055 RMVar_ID_101055 Human_SNP_ID_634715269 m1A Human chr17 - 81891788 81891788 81891788 GGCAGCGCCGGCGTCCGCGCGGGAAGGTATAAAAACGACCACAGTCGCGGCCCGACTCCCTCAAC GGCAGCGCCGGCGTCCGCGCGGGAAGGTATAATAACGACCACAGTCGCGGCCCGACTCCCTCAAC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81891751..81891942 26863196 MeRIP-seq:(Medium) rs1344377269 Functional Loss SNV dbSNP153 33..33 33 - - - 101056 RMVar_ID_101056 Human_SNP_ID_634715836 m1A Human chr17 + 81893554 81893554 81893554 CTGCGGCTAATTTTTTTGTATTTTTTGTAGAGACGGAGTTTCGTCATGTTGGCCAGGCCCATTTG CTGCGGCTAATTTTTTTGTATTTTTTGTAGAGGCGGAGTTTCGTCATGTTGGCCAGGCCCATTTG A G ANAPC11 Ensembl:ENSG00000141552 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81893551..81893625 26863196 MeRIP-seq:(Medium) rs1398455731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765601,Human_RBP_ID_4460133,Human_RBP_ID_5143683,Human_RBP_ID_8941865,Human_RBP_ID_13200910,Human_RBP_ID_22445826,Human_RBP_ID_22587192,Human_RBP_ID_26814154 Human_Splice_Rec_1882330,Human_Splice_Rec_1882331,Human_Splice_Rec_1882336,Human_Splice_Rec_1882337,Human_Splice_Rec_1882342,Human_Splice_Rec_1882343,Human_Splice_Rec_1882352,Human_Splice_Rec_1882353,Human_Splice_Rec_1882358,Human_Splice_Rec_1882359,Human_Splice_Rec_1882370,Human_Splice_Rec_1882371,Human_Splice_Rec_1882386,Human_Splice_Rec_1882387,Human_Splice_Rec_1882390,Human_Splice_Rec_1882391,Human_Splice_Rec_1882398,Human_Splice_Rec_1882399,Human_Splice_Rec_1882404,Human_Splice_Rec_1882405,Human_Splice_Rec_1882414,Human_Splice_Rec_1882415,Human_Splice_Rec_1882420,Human_Splice_Rec_1882421,Human_Splice_Rec_1882431 RMVar_hsa_circ_98397,RMVar_hsa_circ_187785 101057 RMVar_ID_101057 Human_SNP_ID_634716117 m1A Human chr17 + 81894410 81894409 81894410 ACTGTGGCAGGCTTATACCTGTGTTGGTGCCTAAACGTTCTAGCTCTGCAGACTCAATTTAGCCA ACTGTGGCAGGCTTATACCTGTGTTGGTGCCT_AACGTTCTAGCTCTGCAGACTCAATTTAGCCA TA T ANAPC11 Ensembl:ENSG00000141552 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81894405..81894500 26863196 MeRIP-seq:(Medium) rs1330781217 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13200933 RMVar_hsa_circ_98397,RMVar_hsa_circ_187785 101058 RMVar_ID_101058 Human_SNP_ID_634716125 m1A Human chr17 + 81894427 81894427 81894427 CCTGTGTTGGTGCCTAAACGTTCTAGCTCTGCAGACTCAATTTAGCCAGTCGTCCTGTTCCCTCC CCTGTGTTGGTGCCTAAACGTTCTAGCTCTGCCGACTCAATTTAGCCAGTCGTCCTGTTCCCTCC A C ANAPC11 Ensembl:ENSG00000141552 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81894424..81894633 26863196 MeRIP-seq:(Medium) rs763952613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200933 RMVar_hsa_circ_98397,RMVar_hsa_circ_187785 101059 RMVar_ID_101059 Human_SNP_ID_634717943 m1A Human chr17 - 81900130 81900130 81900130 CCTTGTTGCAGCTCAGGGGCGCTGTCCCCAGCAGCCATCGGCGCCAGCATGAGGAAGGAGTCTCA CCTTGTTGCAGCTCAGGGGCGCTGTCCCCAGCTGCCATCGGCGCCAGCATGAGGAAGGAGTCTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81899886..81900150 26863196 MeRIP-seq:(Medium) rs1230986658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18711979 101060 RMVar_ID_101060 Human_SNP_ID_634718618 m1A Human chr17 + 81902210 81902210 81902210 CTCCGCAGCCTCGGCCCGCCCTCGCCGCAGATATAAGGCGGCCCAGGCGGTGGCTGCTCCGAGCC CTCCGCAGCCTCGGCCCGCCCTCGCCGCAGATGTAAGGCGGCCCAGGCGGTGGCTGCTCCGAGCC A G NPB Ensembl:ENSG00000183979 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81902168..81902267 26863196 MeRIP-seq:(Medium) rs1319348316 Functional Loss SNV dbSNP153 33..33 33 - - - 101061 RMVar_ID_101061 Human_SNP_ID_634719107 m1A Human chr17 - 81903391 81903391 81903391 GGCCCCGTAGCAGCATTGGAGGCCAGAGCCCAAGCCAGTTCCGGAGTCACACCCAACGGCGGAGG GGCCCCGTAGCAGCATTGGAGGCCAGAGCCCAGGCCAGTTCCGGAGTCACACCCAACGGCGGAGG T C PCYT2 Ensembl:ENSG00000185813 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81903249..81903540 26863196 MeRIP-seq:(Medium) rs1424520180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18460564,Human_RBP_ID_26759071,Human_RBP_ID_26781762 101062 RMVar_ID_101062 Human_SNP_ID_634724333 m1A Human chr17 + 81917716 81917716 81917716 GACCTTCCCCCGCAGCTCCTCCGGGTCGTCGCACACCTGCCAAGACGCCAGGGTGGTCACCGCCC GACCTTCCCCCGCAGCTCCTCCGGGTCGTCGCCCACCTGCCAAGACGCCAGGGTGGTCACCGCCC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81917690..81917925 26863196 MeRIP-seq:(Medium) rs774595294 Functional Loss SNV dbSNP153 33..33 33 - - - 101063 RMVar_ID_101063 Human_SNP_ID_634724530 m1A Human chr17 + 81918117 81918092 81918117 CGCTCCGCCGCTTTGCGCTCGGAGCGGCTCAGACCCCCGGCTGCCATCGCTCCCCTGGAGACCTG CGCTCCGC_________________________CCCCCGGCTGCCATCGCTCCCCTGGAGACCTG CCGCTTTGCGCTCGGAGCGGCTCAGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81917604..81921446 26863196 MeRIP-seq:(Medium) rs1329345764 Functional Loss DEL dbSNP153 9..33 33 - - - 101064 RMVar_ID_101064 Human_SNP_ID_634725423 m1A Human chr17 - 81921257 81921257 81921257 GTGCCAAGTGGCGCCTGCTGCGTCAGAGCTCAAGGAATCTGTGCCCACCACCAGCTCCTGGTCCG GTGCCAAGTGGCGCCTGCTGCGTCAGAGCTCAGGGAATCTGTGCCCACCACCAGCTCCTGGTCCG T C MAFG,SIRT7 Ensembl:ENSG00000197063,Ensembl:ENSG00000187531 Protein coding,Protein coding 3'UTR,5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1382773331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1545292,Human_RBP_ID_4460301,Human_RBP_ID_13201299,Human_RBP_ID_17127866,Human_RBP_ID_26458487 Human_Splice_Rec_1882775 Human_miRNA_ID_2874085,Human_miRNA_ID_2982047 RMVar_hsa_circ_106600,RMVar_hsa_circ_116913,RMVar_hsa_circ_187796,RMVar_hsa_circ_187797 101065 RMVar_ID_101065 Human_SNP_ID_634725999 m1A Human chr17 + 81922885 81922885 81922885 TCTCCAGCTCCTCCTTCTGCGTCACCCGCTTCACGCGGCAGCTGGCAGCGTAGCCGCGGTTCTTG TCTCCAGCTCCTCCTTCTGCGTCACCCGCTTCTCGCGGCAGCTGGCAGCGTAGCCGCGGTTCTTG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81922836..81923086 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 101066 RMVar_ID_101066 Human_SNP_ID_634726137 m1A Human chr17 - 81923214 81923214 81923214 TCCAGGGTACTGACCTGCTCCGTGTCTTGCAGAGAGCGCCTGCTCGCTGTGCCCCCGGGTTATGA TCCAGGGTACTGACCTGCTCCGTGTCTTGCAGGGAGCGCCTGCTCGCTGTGCCCCCGGGTTATGA T C MAFG Ensembl:ENSG00000197063 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:81923179..81924120 26863410 MeRIP-seq:(Medium) rs1378943919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262843,Human_RBP_ID_901170,Human_RBP_ID_4460339,Human_RBP_ID_5363286,Human_RBP_ID_8190584,Human_RBP_ID_9423141,Human_RBP_ID_18942438,Human_RBP_ID_19080532,Human_RBP_ID_22543936,Human_RBP_ID_22588980,Human_RBP_ID_22657994,Human_RBP_ID_22740424,Human_RBP_ID_26782937 Human_Splice_Rec_1882856,Human_Splice_Rec_1882857,Human_Splice_Rec_1882860,Human_Splice_Rec_1882861,Human_Splice_Rec_1882866,Human_Splice_Rec_1882867 RMVar_hsa_circ_116913,RMVar_hsa_circ_187797 101067 RMVar_ID_101067 Human_SNP_ID_634727264 m1A Human chr17 - 81926460 81926460 81926460 CTGGGTGACAGTGGGCTGGGCAGGGAGGAAGCAGGGGCAGCTCTACCAGGAAACGGCAAAGGGGA CTGGGTGACAGTGGGCTGGGCAGGGAGGAAGCGGGGGCAGCTCTACCAGGAAACGGCAAAGGGGA T C MAFG Ensembl:ENSG00000197063 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81926458..81926583 26863196 MeRIP-seq:(Medium) rs1380225076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542110,Human_RBP_ID_8092355,Human_RBP_ID_8232701,Human_RBP_ID_8727250,Human_RBP_ID_18419782,Human_RBP_ID_22741043 101068 RMVar_ID_101068 Human_SNP_ID_634727365 m1A Human chr17 - 81926789 81926784 81926790 TTAAGTGAGCGCCGAGCGATCCAGTTGAAGGCAGGGGTGCTTGAAGAGGAAGTGGGGGTGGCTCG TTAAGTGAGCGCCGAGCGATCCAGTTGAAGG______TGCTTGAAGAGGAAGTGGGGGTGGCTCG ACCCCTG A MAFG Ensembl:ENSG00000197063 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81926786..81927364 26863196 MeRIP-seq:(Medium) rs879896954 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_9423707,Human_RBP_ID_17189809,Human_RBP_ID_17207025 101069 RMVar_ID_101069 Human_SNP_ID_634727624 m1A Human chr17 + 81927495 81927495 81927495 TCGGCCCCCGCCGCCCCCGCCGCGCCGCCCCCACCGCCCGGGCCCGCCGCCGCAGCCGCACTCAC TCGGCCCCCGCCGCCCCCGCCGCGCCGCCCCCCCCGCCCGGGCCCGCCGCCGCAGCCGCACTCAC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81927492..81927657 26863196 MeRIP-seq:(Medium) rs960841997 Functional Loss SNV dbSNP153 33..33 33 - - - 101070 RMVar_ID_101070 Human_SNP_ID_634727625 m1A Human chr17 + 81927495 81927495 81927495 TCGGCCCCCGCCGCCCCCGCCGCGCCGCCCCCACCGCCCGGGCCCGCCGCCGCAGCCGCACTCAC TCGGCCCCCGCCGCCCCCGCCGCGCCGCCCCCGCCGCCCGGGCCCGCCGCCGCAGCCGCACTCAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81927492..81927657 26863196 MeRIP-seq:(Medium) rs960841997 Functional Loss SNV dbSNP153 33..33 33 - - - 101071 RMVar_ID_101071 Human_SNP_ID_634727632 m1A Human chr17 + 81927531 81927531 81927531 CCCGGGCCCGCCGCCGCAGCCGCACTCACCACACTGCGGGCCCGGCGGGCCGAGGCCGGGGCGGG CCCGGGCCCGCCGCCGCAGCCGCACTCACCACTCTGCGGGCCCGGCGGGCCGAGGCCGGGGCGGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:81927529..81927655 26863196 MeRIP-seq:(Medium) rs1284162101 Functional Loss SNV dbSNP153 33..33 33 - - - 101072 RMVar_ID_101072 Human_SNP_ID_634729513 m1A Human chr17 - 81933374 81933374 81933374 TCCAAAGCCAACCTCTCCCTGCCTCTCTAGGGAGCTGCAGTCCATGGCTGACCAGGAGCAGGTGT TCCAAAGCCAACCTCTCCCTGCCTCTCTAGGGTGCTGCAGTCCATGGCTGACCAGGAGCAGGTGT T A PYCR1 Ensembl:ENSG00000183010 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81933326..81933400 32194978 MeRIP-seq:(Medium) rs901236548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897095,Human_RBP_ID_22543938,Human_RBP_ID_22657063 Human_Splice_Rec_1882886,Human_Splice_Rec_1882887,Human_Splice_Rec_1882900,Human_Splice_Rec_1882912,Human_Splice_Rec_1882926,Human_Splice_Rec_1882938,Human_Splice_Rec_1882948,Human_Splice_Rec_1882956,Human_Splice_Rec_1882970,Human_Splice_Rec_1882982 RMVar_hsa_circ_87352,RMVar_hsa_circ_112525,RMVar_hsa_circ_187799,RMVar_hsa_circ_83403,RMVar_hsa_circ_187800,RMVar_hsa_circ_187798 101073 RMVar_ID_101073 Human_SNP_ID_634729987 m1A Human chr17 - 81934703 81934703 81934703 CCCTGGATGCCCTGGCTGATGGGGGTGTGAAGATGGGACTTCCAAGGCGCCTGGCAGTCCGCCTC CCCTGGATGCCCTGGCTGATGGGGGTGTGAAGGTGGGACTTCCAAGGCGCCTGGCAGTCCGCCTC T C PYCR1 Ensembl:ENSG00000183010 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81934653..81934761 26863196 MeRIP-seq:(Medium) rs772085912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951408,Human_RBP_ID_9377125,Human_RBP_ID_22444059 Human_Splice_Rec_1882882,Human_Splice_Rec_1882883,Human_Splice_Rec_1882910,Human_Splice_Rec_1882911,Human_Splice_Rec_1882922,Human_Splice_Rec_1882923,Human_Splice_Rec_1882934,Human_Splice_Rec_1882935,Human_Splice_Rec_1882946,Human_Splice_Rec_1882947,Human_Splice_Rec_1882966,Human_Splice_Rec_1882967,Human_Splice_Rec_1882978,Human_Splice_Rec_1882979,Human_Splice_Rec_1882992,Human_Splice_Rec_1882993,Human_Splice_Rec_1883004,Human_Splice_Rec_1883005,Human_Splice_Rec_1883014 RMVar_hsa_circ_102346,RMVar_hsa_circ_112525,RMVar_hsa_circ_187799,RMVar_hsa_circ_83403,RMVar_hsa_circ_187800,RMVar_hsa_circ_187801 101074 RMVar_ID_101074 Human_SNP_ID_634730145 m1A Human chr17 + 81935023 81935023 81935023 AGAAGCCCACGCTGCTCAGCAGCTGCTCCATGAGCCTCCCGTCCTCCACCTGGGCGTGCGTGCCT AGAAGCCCACGCTGCTCAGCAGCTGCTCCATGGGCCTCCCGTCCTCCACCTGGGCGTGCGTGCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81934976..81935025 32194978 MeRIP-seq:(Medium) rs1219327272 Functional Loss SNV dbSNP153 33..33 33 - - - 101075 RMVar_ID_101075 Human_SNP_ID_634730152 m1A Human chr17 - 81935032 81935032 81935032 GTATGCCACAGGCACGCACGCCCAGGTGGAGGACGGGAGGCTCATGGAGCAGCTGCTGAGCAGCG GTATGCCACAGGCACGCACGCCCAGGTGGAGGTCGGGAGGCTCATGGAGCAGCTGCTGAGCAGCG T A PYCR1 Ensembl:ENSG00000183010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81934982..81935099 26863196 MeRIP-seq:(Medium) rs773796809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22445142,Human_RBP_ID_23755394 Human_miRNA_ID_1967440,Human_miRNA_ID_2209454,Human_miRNA_ID_3034060 RMVar_hsa_circ_102346,RMVar_hsa_circ_112525,RMVar_hsa_circ_187799,RMVar_hsa_circ_83403,RMVar_hsa_circ_187800,RMVar_hsa_circ_187801 101076 RMVar_ID_101076 Human_SNP_ID_634730174 m1A Human chr17 - 81935057 81935057 81935057 TCGTGGTGCGGGAGGGGGCCACCGTGTATGCCACAGGCACGCACGCCCAGGTGGAGGACGGGAGG TCGTGGTGCGGGAGGGGGCCACCGTGTATGCCGCAGGCACGCACGCCCAGGTGGAGGACGGGAGG T C PYCR1 Ensembl:ENSG00000183010 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81935006..81935093 26863196 MeRIP-seq:(Medium) rs1243324455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503169,Human_RBP_ID_766483,Human_RBP_ID_821948,Human_RBP_ID_23755394 Human_Splice_Rec_1882880,Human_Splice_Rec_1882896,Human_Splice_Rec_1882908,Human_Splice_Rec_1882920,Human_Splice_Rec_1882932,Human_Splice_Rec_1882944,Human_Splice_Rec_1882954,Human_Splice_Rec_1882964,Human_Splice_Rec_1882976,Human_Splice_Rec_1882990,Human_Splice_Rec_1883002,Human_Splice_Rec_1883012,Human_Splice_Rec_1883022,Human_Splice_Rec_1883028,Human_Splice_Rec_1883036 RMVar_hsa_circ_102346,RMVar_hsa_circ_112525,RMVar_hsa_circ_187799,RMVar_hsa_circ_83403,RMVar_hsa_circ_187800,RMVar_hsa_circ_187801 101077 RMVar_ID_101077 Human_SNP_ID_634730964 m1A Human chr17 + 81937212 81937212 81937212 CGTCGCGCCCCACCCGGCGACCGCCGCCCACCATTCCCGGAGCCCGACCCCAACCCAGCTACCGT CGTCGCGCCCCACCCGGCGACCGCCGCCCACCGTTCCCGGAGCCCGACCCCAACCCAGCTACCGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81936851..81937300 26863196 MeRIP-seq:(Medium) rs1260399612 Functional Loss SNV dbSNP153 33..33 33 - - - 101078 RMVar_ID_101078 Human_SNP_ID_634736561 m1A Human chr17 - 81954149 81954148 81954149 TGGCCTCCCATGGGCCTCTTCTTGGCGCTTCTAGGGGTGGGATTTCCTTATAGGGGTGCCAGAGC TGGCCTCCCATGGGCCTCTTCTTGGCGCTTCT_GGGGTGGGATTTCCTTATAGGGGTGCCAGAGC CT C NOTUM Ensembl:ENSG00000185269 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81954144..81954277 26863196 MeRIP-seq:(Medium) rs1180788679 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18164400,Human_RBP_ID_21974752 101079 RMVar_ID_101079 Human_SNP_ID_634736563 m1A Human chr17 + 81954152 81954149 81954152 CTGGCACCCCTATAAGGAAATCCCACCCCTAGAAGCGCCAAGAAGAGGCCCATGGGAGGCCAAGT CTGGCACCCCTATAAGGAAATCCCACCCCT___AGCGCCAAGAAGAGGCCCATGGGAGGCCAAGT TAGA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81954149..81954246 26863196 MeRIP-seq:(Medium) rs961239973 Functional Loss DEL dbSNP153 31..33 33 - - - 101080 RMVar_ID_101080 Human_SNP_ID_634737092 m1A Human chr17 + 81955540 81955540 81955540 GCCTCGTCAAACAGCCACTGCACCACGAACACAGGGCCTGCGGGCGGCGGGGCTCAGTTCGGCCT GCCTCGTCAAACAGCCACTGCACCACGAACACGGGGCCTGCGGGCGGCGGGGCTCAGTTCGGCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81955528..81955612 26863196 MeRIP-seq:(Medium) rs768738123 Functional Loss SNV dbSNP153 33..33 33 - - - 101081 RMVar_ID_101081 Human_SNP_ID_634737215 m1A Human chr17 + 81955859 81955859 81955859 CCCCATCCCAGGCTCAGAGCTCAGCACCCCCCAGGCCCCTGCAGTGCCCCCTATCCCAGGCTCAG CCCCATCCCAGGCTCAGAGCTCAGCACCCCCCCGGCCCCTGCAGTGCCCCCTATCCCAGGCTCAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81955809..81956011 26863196 MeRIP-seq:(Medium) rs1316833719 Functional Loss SNV dbSNP153 33..33 33 - - - 101082 RMVar_ID_101082 Human_SNP_ID_634745132 m1A Human chr17 + 81979238 81979238 81979238 GGCAGGACTTCAACCCCTGTGAATATGATCTGAAGTGAGTTTGCTCCAGCTCAGCAGCAGGGTCT GGCAGGACTTCAACCCCTGTGAATATGATCTGCAGTGAGTTTGCTCCAGCTCAGCAGCAGGGTCT A C ASPSCR1 Ensembl:ENSG00000169696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr17:81979089..81979250;chr17:81978776..81982630 26863196,32194978 MeRIP-seq:(Medium) rs1445357999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084596 Human_Splice_Rec_1883110,Human_Splice_Rec_1883111,Human_Splice_Rec_1883122,Human_Splice_Rec_1883123,Human_Splice_Rec_1883154,Human_Splice_Rec_1883155,Human_Splice_Rec_1883168,Human_Splice_Rec_1883169,Human_Splice_Rec_1883198,Human_Splice_Rec_1883199,Human_Splice_Rec_1883234,Human_Splice_Rec_1883235,Human_Splice_Rec_1883246,Human_Splice_Rec_1883247,Human_Splice_Rec_1883256,Human_Splice_Rec_1883257,Human_Splice_Rec_1883260,Human_Splice_Rec_1883261 RMVar_hsa_circ_32511,RMVar_hsa_circ_119350,RMVar_hsa_circ_288739,RMVar_hsa_circ_56317,RMVar_hsa_circ_187807,RMVar_hsa_circ_27983,RMVar_hsa_circ_187808,RMVar_hsa_circ_187806 101083 RMVar_ID_101083 Human_SNP_ID_634747660 m1A Human chr17 - 81986764 81986763 81986765 AGCCCTGGGGCCACCAAGCGCGCCCAACGCACAGTCACCTTCCCAGCGCCCGACGCGCGGTCACC AGCCCTGGGGCCACCAAGCGCGCCCAACGCA__GTCACCTTCCCAGCGCCCGACGCGCGGTCACC CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81986762..81987603 26863196 MeRIP-seq:(Medium) rs1330841256 Functional Loss DEL dbSNP153 32..33 33 - - - 101084 RMVar_ID_101084 Human_SNP_ID_634747661 m1A Human chr17 - 81986764 81986764 81986764 AGCCCTGGGGCCACCAAGCGCGCCCAACGCACAGTCACCTTCCCAGCGCCCGACGCGCGGTCACC AGCCCTGGGGCCACCAAGCGCGCCCAACGCACGGTCACCTTCCCAGCGCCCGACGCGCGGTCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81986762..81987603 26863196 MeRIP-seq:(Medium) rs952872658 Functional Loss SNV dbSNP153 33..33 33 - - - 101085 RMVar_ID_101085 Human_SNP_ID_634747793 m1A Human chr17 + 81987138 81987138 81987138 AGGGGTGAGCGGGACCCGAGGCAGGAGGTGACAGAGCCTAAGAGCAAAGCGAAGCCACGGGCAGG AGGGGTGAGCGGGACCCGAGGCAGGAGGTGACGGAGCCTAAGAGCAAAGCGAAGCCACGGGCAGG A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81987015..81987503 26863196 MeRIP-seq:(Medium) rs531189801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119350,RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_187806 101086 RMVar_ID_101086 Human_SNP_ID_634747941 m1A Human chr17 + 81987626 81987626 81987626 GGGCCGAGGGTGTCTGGAGAGGTGGGGCCGGCATTGTGGTAGCATAAGCCTCTTCAACAGACTTT GGGCCGAGGGTGTCTGGAGAGGTGGGGCCGGCGTTGTGGTAGCATAAGCCTCTTCAACAGACTTT A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81987620..81987836 26863196 MeRIP-seq:(Medium) rs1175686916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119350,RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_187806 101087 RMVar_ID_101087 Human_SNP_ID_634749307 m1A Human chr17 + 81992124 81992124 81992124 GCGAGCAGGCACCCGCGGAAGCGCCCCAAAGCACTTCTTGCATTTCTGGCTTCGGAGCATGGTGT GCGAGCAGGCACCCGCGGAAGCGCCCCAAAGCGCTTCTTGCATTTCTGGCTTCGGAGCATGGTGT A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81992121..81992252 26863196 MeRIP-seq:(Medium) rs1251886329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119350,RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_187806 101088 RMVar_ID_101088 Human_SNP_ID_634750935 m1A Human chr17 + 81996806 81996806 81996806 GGGCCAGGATCCCCAGCAGGAGCAGGAGCAGGAGCGGGAGCGGGATCCCCAGCAGGAGCAGGAGC GGGCCAGGATCCCCAGCAGGAGCAGGAGCAGGGGCGGGAGCGGGATCCCCAGCAGGAGCAGGAGC A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81996705..81996879 26863196 MeRIP-seq:(Medium) rs1329259900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18992933 Human_Splice_Rec_1883133,Human_Splice_Rec_1883179,Human_Splice_Rec_1883215,Human_Splice_Rec_1883271,Human_Splice_Rec_1883295 RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_187811,RMVar_hsa_circ_331513,RMVar_hsa_circ_55539 101089 RMVar_ID_101089 Human_SNP_ID_634753263 m1A Human chr17 + 82004220 82004220 82004220 TCCCTCCCCTCGGTTTCCCAGCTCAGCGGCCCAGGGATGCCCCAGCACTGTCTGCTGTGAGGCCG TCCCTCCCCTCGGTTTCCCAGCTCAGCGGCCCGGGGATGCCCCAGCACTGTCTGCTGTGAGGCCG A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82004216..82004281 26863196 MeRIP-seq:(Medium) rs1394520774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3544306,Human_RBP_ID_8727274,Human_RBP_ID_18420360,Human_RBP_ID_22416262,Human_RBP_ID_22717142,Human_RBP_ID_22740719 RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539 101090 RMVar_ID_101090 Human_SNP_ID_634754972 m1A Human chr17 + 82009479 82009479 82009479 TCTGACCAGAAGCCCTGTTCCTTCCCCTCCTCACCACAGGAAGCGCCTGGAAGAAGCCCCCTTGG TCTGACCAGAAGCCCTGTTCCTTCCCCTCCTCGCCACAGGAAGCGCCTGGAAGAAGCCCCCTTGG A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82009476..82009500 26863196 MeRIP-seq:(Medium) rs1285997206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1883137,Human_Splice_Rec_1883183,Human_Splice_Rec_1883219,Human_Splice_Rec_1883243,Human_Splice_Rec_1883275,Human_Splice_Rec_1883299,Human_Splice_Rec_1883313,Human_Splice_Rec_1883329,Human_Splice_Rec_1883343,Human_Splice_Rec_1883357 RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539,RMVar_hsa_circ_20908 101091 RMVar_ID_101091 Human_SNP_ID_634757236 m1A Human chr17 - 82015288 82015288 82015288 TCGGGAGGGATCGCCACTGCTCGGACGAGGGGATGGTGGAGAGGAGGGTCGGCAGACTGGGTGGC TCGGGAGGGATCGCCACTGCTCGGACGAGGGGGTGGTGGAGAGGAGGGTCGGCAGACTGGGTGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82015282..82015409 26863196 MeRIP-seq:(Medium) rs765479614 Functional Loss SNV dbSNP153 33..33 33 - - - 101092 RMVar_ID_101092 Human_SNP_ID_634757680 m1A Human chr17 + 82016526 82016526 82016526 GCTCTGGTGCACTTGGGAGCCGAGGAGCCGGCAGGTGAGTGTCAGTGGTTGGGGCCAGTGTCGGA GCTCTGGTGCACTTGGGAGCCGAGGAGCCGGCGGGTGAGTGTCAGTGGTTGGGGCCAGTGTCGGA A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82016476..82016550 26863196 MeRIP-seq:(Medium) rs757952986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5365520,Human_RBP_ID_18989633,Human_RBP_ID_19080579,Human_RBP_ID_22959697,Human_RBP_ID_23118990 Human_Splice_Rec_1883146,Human_Splice_Rec_1883147,Human_Splice_Rec_1883190,Human_Splice_Rec_1883191,Human_Splice_Rec_1883226,Human_Splice_Rec_1883227,Human_Splice_Rec_1883284,Human_Splice_Rec_1883285,Human_Splice_Rec_1883306,Human_Splice_Rec_1883307,Human_Splice_Rec_1883320,Human_Splice_Rec_1883321,Human_Splice_Rec_1883336,Human_Splice_Rec_1883337,Human_Splice_Rec_1883350,Human_Splice_Rec_1883351,Human_Splice_Rec_1883364,Human_Splice_Rec_1883372,Human_Splice_Rec_1883373,Human_Splice_Rec_1883380,Human_Splice_Rec_1883381,Human_Splice_Rec_1883388,Human_Splice_Rec_1883389,Human_Splice_Rec_1883398,Human_Splice_Rec_1883399,Human_Splice_Rec_1883406,Human_Splice_Rec_1883407 RMVar_hsa_circ_27983 101093 RMVar_ID_101093 Human_SNP_ID_634757915 m1A Human chr17 - 82017040 82017038 82017040 TTCACGGGCTGGGCCGTCCCTGGGATGGGCTCAGGGGGGACCAGCGCCCCCTCCTCAGCAGCTGG TTCACGGGCTGGGCCGTCCCTGGGATGGGCTC__GGGGGACCAGCGCCCCCTCCTCAGCAGCTGG CCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82017026..82017075 26863196 MeRIP-seq:(Medium) rs777308203 Functional Loss DEL dbSNP153 33..34 33 - - - 101094 RMVar_ID_101094 Human_SNP_ID_634757918 m1A Human chr17 - 82017040 82017039 82017040 TTCACGGGCTGGGCCGTCCCTGGGATGGGCTCAGGGGGGACCAGCGCCCCCTCCTCAGCAGCTGG TTCACGGGCTGGGCCGTCCCTGGGATGGGCTC_GGGGGGACCAGCGCCCCCTCCTCAGCAGCTGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82017026..82017075 26863196 MeRIP-seq:(Medium) rs759152306 Functional Loss DEL dbSNP153 33..33 33 - - - 101095 RMVar_ID_101095 Human_SNP_ID_634757920 m1A Human chr17 - 82017040 82017040 82017040 TTCACGGGCTGGGCCGTCCCTGGGATGGGCTCAGGGGGGACCAGCGCCCCCTCCTCAGCAGCTGG TTCACGGGCTGGGCCGTCCCTGGGATGGGCTCTGGGGGGACCAGCGCCCCCTCCTCAGCAGCTGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82017026..82017075 26863196 MeRIP-seq:(Medium) rs771528983 Functional Loss SNV dbSNP153 33..33 33 - - - 101096 RMVar_ID_101096 Human_SNP_ID_634758708 m1A Human chr17 - 82019153 82019153 82019153 GGCCACCCCCAGAGGAGCCCCTGGTCCACAGAAGCAGGCCTTGTGTTTCCAGCGGCCTCTGATAA GGCCACCCCCAGAGGAGCCCCTGGTCCACAGATGCAGGCCTTGTGTTTCCAGCGGCCTCTGATAA T A CENPX Ensembl:ENSG00000169689 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1433608027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503209,Human_RBP_ID_1871104,Human_RBP_ID_5368579,Human_RBP_ID_19080584,Human_RBP_ID_26330937,Human_RBP_ID_27262685 Human_Splice_Rec_1883418,Human_Splice_Rec_1883426,Human_Splice_Rec_1883434,Human_Splice_Rec_1883440,Human_Splice_Rec_1883446,Human_Splice_Rec_1883454,Human_Splice_Rec_1883462,Human_Splice_Rec_1883474,Human_Splice_Rec_1883482,Human_Splice_Rec_1883486 Human_miRNA_ID_1093685 RMVar_hsa_circ_82225,RMVar_hsa_circ_114705,RMVar_hsa_circ_103014,RMVar_hsa_circ_187814,RMVar_hsa_circ_187815,RMVar_hsa_circ_187813 101097 RMVar_ID_101097 Human_SNP_ID_634758839 m1A Human chr17 + 82019363 82019363 82019363 CACGGAGCGCGTCTTCTGCCTGGGCCTGCCGCACGCCGCGGACTGCTGCTTCTGCGGTGAGAAAC CACGGAGCGCGTCTTCTGCCTGGGCCTGCCGCGCGCCGCGGACTGCTGCTTCTGCGGTGAGAAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:82018759..82019400;chr17:82019204..82019401 26863196 MeRIP-seq:(Medium) rs909402906 Functional Loss SNV dbSNP153 33..33 33 - - - 101098 RMVar_ID_101098 Human_SNP_ID_634759680 m1A Human chr17 - 82021708 82021708 82021708 CTGGGTACACACCCCAGGAGGTCATGTGTTCTATCAAGCCCACCTGACAACTAGAGGCCCAGGGG CTGGGTACACACCCCAGGAGGTCATGTGTTCTGTCAAGCCCACCTGACAACTAGAGGCCCAGGGG T C CENPX Ensembl:ENSG00000169689 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82021706..82021877 26863196 MeRIP-seq:(Medium) rs1202614169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82225,RMVar_hsa_circ_187815 101099 RMVar_ID_101099 Human_SNP_ID_634759889 m1A Human chr17 + 82022329 82022329 82022329 GGGTTAATCCCTGTCAAGTGTGTGTAACGTGGAGCACCGAAGAAACCACGCGTTCCTAGCCCAGT GGGTTAATCCCTGTCAAGTGTGTGTAACGTGGGGCACCGAAGAAACCACGCGTTCCTAGCCCAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82022325..82022900 26863196 MeRIP-seq:(Medium) rs575156482 Functional Loss SNV dbSNP153 33..33 33 - - - 101100 RMVar_ID_101100 Human_SNP_ID_634759955 m1A Human chr17 - 82022576 82022575 82022576 CGGGAAGGTGGAGAGGGTCTGCAGAAACAGGCAGGGGTGGGCGCCGTCACGGCGGAGTCCAAGCC CGGGAAGGTGGAGAGGGTCTGCAGAAACAGGC_GGGGTGGGCGCCGTCACGGCGGAGTCCAAGCC CT C CENPX Ensembl:ENSG00000169689 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82022572..82022900 26863196 MeRIP-seq:(Medium) rs1035227580 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3542136,Human_RBP_ID_5319413,Human_RBP_ID_5362278,Human_RBP_ID_8092381,Human_RBP_ID_8190664,Human_RBP_ID_9423715,Human_RBP_ID_18420399,Human_RBP_ID_22657085,Human_RBP_ID_22741053 RMVar_hsa_circ_82225,RMVar_hsa_circ_187815 101101 RMVar_ID_101101 Human_SNP_ID_634759956 m1A Human chr17 - 82022576 82022576 82022576 CGGGAAGGTGGAGAGGGTCTGCAGAAACAGGCAGGGGTGGGCGCCGTCACGGCGGAGTCCAAGCC CGGGAAGGTGGAGAGGGTCTGCAGAAACAGGCGGGGGTGGGCGCCGTCACGGCGGAGTCCAAGCC T C CENPX Ensembl:ENSG00000169689 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82022572..82022900 26863196 MeRIP-seq:(Medium) rs956238945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542136,Human_RBP_ID_5319413,Human_RBP_ID_5362278,Human_RBP_ID_8092381,Human_RBP_ID_8190664,Human_RBP_ID_9423715,Human_RBP_ID_18420399,Human_RBP_ID_22657085,Human_RBP_ID_22741053 RMVar_hsa_circ_82225,RMVar_hsa_circ_187815 101102 RMVar_ID_101102 Human_SNP_ID_634760014 m1A Human chr17 + 82022759 82022757 82022759 GGGGGCGGCGCGGGGGCTGGCGTCTGGCCCTCACAGTGTCACGCGTGAGGTCGGGACGGAGCGTC GGGGGCGGCGCGGGGGCTGGCGTCTGGCCCT__CAGTGTCACGCGTGAGGTCGGGACGGAGCGTC TCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82022757..82022900 26863196 MeRIP-seq:(Medium) rs1482532972 Functional Loss DEL dbSNP153 32..33 33 - - - 101103 RMVar_ID_101103 Human_SNP_ID_634760015 m1A Human chr17 + 82022759 82022759 82022759 GGGGGCGGCGCGGGGGCTGGCGTCTGGCCCTCACAGTGTCACGCGTGAGGTCGGGACGGAGCGTC GGGGGCGGCGCGGGGGCTGGCGTCTGGCCCTCTCAGTGTCACGCGTGAGGTCGGGACGGAGCGTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82022757..82022900 26863196 MeRIP-seq:(Medium) rs1184142816 Functional Loss SNV dbSNP153 33..33 33 - - - 101104 RMVar_ID_101104 Human_SNP_ID_634760529 m1A Human chr17 - 82023782 82023782 82023782 CTCCCTCGGCAGCAGCTTGCCCAGGGCCCTGCAGGTCTCCACCGTCAGGCTTTGCGTGGCCAGGT CTCCCTCGGCAGCAGCTTGCCCAGGGCCCTGCTGGTCTCCACCGTCAGGCTTTGCGTGGCCAGGT T A CENPX Ensembl:ENSG00000169689 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82023627..82023875 26863196 MeRIP-seq:(Medium) rs1420426247 Functional Loss SNV dbSNP153 33..33 33 - - - 101105 RMVar_ID_101105 Human_SNP_ID_634760884 m1A Human chr17 - 82024704 82024704 82024704 AGTTTTCCCAGAGCCTCGGCCCCTGCAGCCCGAAGGTTGTTGCCCTAGGAGAGAAACAGGCCGGT AGTTTTCCCAGAGCCTCGGCCCCTGCAGCCCGTAGGTTGTTGCCCTAGGAGAGAAACAGGCCGGT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82024700..82025134 32194978 MeRIP-seq:(Medium) rs1261068365 Functional Loss SNV dbSNP153 33..33 33 - - - 101106 RMVar_ID_101106 Human_SNP_ID_634760885 m1A Human chr17 - 82024704 82024704 82024704 AGTTTTCCCAGAGCCTCGGCCCCTGCAGCCCGAAGGTTGTTGCCCTAGGAGAGAAACAGGCCGGT AGTTTTCCCAGAGCCTCGGCCCCTGCAGCCCGCAGGTTGTTGCCCTAGGAGAGAAACAGGCCGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82024700..82025134 32194978 MeRIP-seq:(Medium) rs1261068365 Functional Loss SNV dbSNP153 33..33 33 - - - 101107 RMVar_ID_101107 Human_SNP_ID_634761215 m1A Human chr17 - 82025505 82025505 82025505 CGCGTCACTCCACACAGCCCTGCACCGTACCCACGGCTCTGAGGACGTCTCCAGGGATGTTGTTC CGCGTCACTCCACACAGCCCTGCACCGTACCCGCGGCTCTGAGGACGTCTCCAGGGATGTTGTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82025497..82025642 26863196 MeRIP-seq:(Medium) rs1465402544 Functional Loss SNV dbSNP153 33..33 33 - - - 101108 RMVar_ID_101108 Human_SNP_ID_634761225 m1A Human chr17 - 82025524 82025524 82025524 GGCCTCTGTCAAAGGCTCACGCGTCACTCCACACAGCCCTGCACCGTACCCACGGCTCTGAGGAC GGCCTCTGTCAAAGGCTCACGCGTCACTCCACGCAGCCCTGCACCGTACCCACGGCTCTGAGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82025522..82025619 26863196 MeRIP-seq:(Medium) rs1388913482 Functional Loss SNV dbSNP153 33..33 33 - - - 101109 RMVar_ID_101109 Human_SNP_ID_634762782 m1A Human chr17 + 82029563 82029563 82029563 CCATCTGTGCAGGAGCTGAGCCGAGTGAAAGCAGCGGCACTCAGCGAGCGTGGCCAGGCTGAGGA CCATCTGTGCAGGAGCTGAGCCGAGTGAAAGCGGCGGCACTCAGCGAGCGTGGCCAGGCTGAGGA A G LRRC45 Ensembl:ENSG00000169683 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82029026..82030933 26863196 MeRIP-seq:(Medium) rs1481164301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898938,Human_RBP_ID_18712076,Human_RBP_ID_18989653,Human_RBP_ID_23257053 Human_Splice_Rec_1883512,Human_Splice_Rec_1883513,Human_Splice_Rec_1883558,Human_Splice_Rec_1883559 RMVar_hsa_circ_267138 101110 RMVar_ID_101110 Human_SNP_ID_634763300 m1A Human chr17 - 82030760 82030746 82030761 CTCAGGGTCCTCACGGGGGACGCCTGCACGTAAGCCAGGACGGCGTTCTGCAGGAAGCTCGCCCT CTCAGGGTCCTCACGGGGGACGCCTGCACGT_______________TCTGCAGGAAGCTCGCCCT AACGCCGTCCTGGCTT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82030726..82030930 26863196 MeRIP-seq:(Medium) rs1186959502 Functional Loss DEL dbSNP153 32..46 33 - - - 101111 RMVar_ID_101111 Human_SNP_ID_634763875 m1A Human chr17 - 82032063 82032063 82032063 CCCAGGTGAGAGGCCTGGCCCCACCCACTGGGAGGACAGGGCGGCGGCCCCGCCTCGCCCGCAGC CCCAGGTGAGAGGCCTGGCCCCACCCACTGGGGGGACAGGGCGGCGGCCCCGCCTCGCCCGCAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82032024..82032223 26863196 MeRIP-seq:(Medium) rs1210555008 Functional Loss SNV dbSNP153 33..33 33 - - - 101112 RMVar_ID_101112 Human_SNP_ID_634764624 m1A Human chr17 + 82033797 82033797 82033797 CGATCCGCGCGGTGCTCTGCCCGCCCCCAGTGAAGAAGCCGGGGAAGAAGTGCACCGTCTTCTAG CGATCCGCGCGGTGCTCTGCCCGCCCCCAGTGGAGAAGCCGGGGAAGAAGTGCACCGTCTTCTAG A G RAC3 Ensembl:ENSG00000169750 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82033746..82033900 26863196 MeRIP-seq:(Medium) rs771801066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503248,Human_RBP_ID_8466565,Human_RBP_ID_17903212,Human_RBP_ID_22959983 Human_Splice_Rec_1883576,Human_Splice_Rec_1883584,Human_Splice_Rec_1883592,Human_Splice_Rec_1883596 RMVar_hsa_circ_187817 101113 RMVar_ID_101113 Human_SNP_ID_634764670 m1A Human chr17 + 82033865 82033865 82033865 CCTGGCCCACCCGAGCCTGAGGGCTGGCGGGGAGCAGCCCTGGACGTGTCCGCTGTTGTGTTGAG CCTGGCCCACCCGAGCCTGAGGGCTGGCGGGGGGCAGCCCTGGACGTGTCCGCTGTTGTGTTGAG A G RAC3 Ensembl:ENSG00000169750 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82033814..82033911 26863196 MeRIP-seq:(Medium) rs775843344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503248,Human_RBP_ID_4460705,Human_RBP_ID_18712086,Human_RBP_ID_18989660,Human_RBP_ID_23755508 RMVar_hsa_circ_187817 101114 RMVar_ID_101114 Human_SNP_ID_634764772 m1A Human chr17 - 82034113 82034113 82034113 AGGAACAGAACTCCCCCCCACCCTCCCCCTCCAGGGAAGCCCATCCTGGGGCTTCCCTGCACCTG AGGAACAGAACTCCCCCCCACCCTCCCCCTCCCGGGAAGCCCATCCTGGGGCTTCCCTGCACCTG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:82034013..82034135 26863410 MeRIP-seq:(Medium) rs1227894913 Functional Loss SNV dbSNP153 33..33 33 - - - 101115 RMVar_ID_101115 Human_SNP_ID_634765618 m1A Human chr17 - 82036294 82036294 82036294 CCAGCTGTCCCGGTGTAGATCCGAGTGAATGCAGTAAACCCCACAGTGGTGATGACGTCCATGGG CCAGCTGTCCCGGTGTAGATCCGAGTGAATGCGGTAAACCCCACAGTGGTGATGACGTCCATGGG T C DCXR Ensembl:ENSG00000169738 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs968889938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503277,Human_RBP_ID_5115699,Human_RBP_ID_8466578,Human_RBP_ID_9077083,Human_RBP_ID_17653982,Human_RBP_ID_22445149,Human_RBP_ID_23257054,Human_RBP_ID_23755518 Human_Splice_Rec_1883604,Human_Splice_Rec_1883618,Human_Splice_Rec_1883622,Human_Splice_Rec_1883634,Human_Splice_Rec_1883646,Human_Splice_Rec_1883650,Human_Splice_Rec_1883658,Human_Splice_Rec_1883698,Human_Splice_Rec_1883710,Human_Splice_Rec_1883724,Human_Splice_Rec_1883734,Human_Splice_Rec_1883740,Human_Splice_Rec_1883744,Human_Splice_Rec_1883754 Human_miRNA_ID_2172419,Human_miRNA_ID_2172420,Human_miRNA_ID_2235412,Human_miRNA_ID_2235413,Human_miRNA_ID_2298705,Human_miRNA_ID_2298706,Human_miRNA_ID_2950721,Human_miRNA_ID_2950722,Human_miRNA_ID_3029577,Human_miRNA_ID_3029578 RMVar_hsa_circ_112394,RMVar_hsa_circ_119576,RMVar_hsa_circ_126591,RMVar_hsa_circ_121723,RMVar_hsa_circ_117830,RMVar_hsa_circ_187818,RMVar_hsa_circ_187822,RMVar_hsa_circ_84182,RMVar_hsa_circ_102864,RMVar_hsa_circ_187824,RMVar_hsa_circ_187823,RMVar_hsa_circ_187820,RMVar_hsa_circ_187821,RMVar_hsa_circ_187819,RMVar_hsa_circ_187827,RMVar_hsa_circ_108393,RMVar_hsa_circ_187826 101116 RMVar_ID_101116 Human_SNP_ID_634765619 m1A Human chr17 - 82036294 82036294 82036294 CCAGCTGTCCCGGTGTAGATCCGAGTGAATGCAGTAAACCCCACAGTGGTGATGACGTCCATGGG CCAGCTGTCCCGGTGTAGATCCGAGTGAATGCCGTAAACCCCACAGTGGTGATGACGTCCATGGG T G DCXR Ensembl:ENSG00000169738 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs968889938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503277,Human_RBP_ID_5115699,Human_RBP_ID_8466578,Human_RBP_ID_9077083,Human_RBP_ID_17653982,Human_RBP_ID_22445149,Human_RBP_ID_23257054,Human_RBP_ID_23755518 Human_Splice_Rec_1883604,Human_Splice_Rec_1883618,Human_Splice_Rec_1883622,Human_Splice_Rec_1883634,Human_Splice_Rec_1883646,Human_Splice_Rec_1883650,Human_Splice_Rec_1883658,Human_Splice_Rec_1883698,Human_Splice_Rec_1883710,Human_Splice_Rec_1883724,Human_Splice_Rec_1883734,Human_Splice_Rec_1883740,Human_Splice_Rec_1883744,Human_Splice_Rec_1883754 Human_miRNA_ID_2172419,Human_miRNA_ID_2172420,Human_miRNA_ID_2235412,Human_miRNA_ID_2235413,Human_miRNA_ID_2298705,Human_miRNA_ID_2298706,Human_miRNA_ID_2950721,Human_miRNA_ID_2950722,Human_miRNA_ID_3029577,Human_miRNA_ID_3029578 RMVar_hsa_circ_112394,RMVar_hsa_circ_119576,RMVar_hsa_circ_126591,RMVar_hsa_circ_121723,RMVar_hsa_circ_117830,RMVar_hsa_circ_187818,RMVar_hsa_circ_187822,RMVar_hsa_circ_84182,RMVar_hsa_circ_102864,RMVar_hsa_circ_187824,RMVar_hsa_circ_187823,RMVar_hsa_circ_187820,RMVar_hsa_circ_187821,RMVar_hsa_circ_187819,RMVar_hsa_circ_187827,RMVar_hsa_circ_108393,RMVar_hsa_circ_187826 101117 RMVar_ID_101117 Human_SNP_ID_634765871 m1A Human chr17 - 82036806 82036805 82036806 GAACCTCAGGGAGGGGCTGTCCTGGAGGACGCAGCAGCCCTAATCTCTGACCAGGGTCTGTCCCT GAACCTCAGGGAGGGGCTGTCCTGGAGGACGC_GCAGCCCTAATCTCTGACCAGGGTCTGTCCCT CT C DCXR Ensembl:ENSG00000169738 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82036805..82036903 32194978 MeRIP-seq:(Medium) rs766445378 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22657095 Human_Splice_Rec_1883599,Human_Splice_Rec_1883613,Human_Splice_Rec_1883629,Human_Splice_Rec_1883641,Human_Splice_Rec_1883675,Human_Splice_Rec_1883681,Human_Splice_Rec_1883693,Human_Splice_Rec_1883705,Human_Splice_Rec_1883719,Human_Splice_Rec_1883729,Human_Splice_Rec_1883749,Human_Splice_Rec_1883759,Human_Splice_Rec_1883765,Human_Splice_Rec_1883768,Human_Splice_Rec_1883771,Human_Splice_Rec_1883777 RMVar_hsa_circ_112394,RMVar_hsa_circ_121723,RMVar_hsa_circ_187818,RMVar_hsa_circ_102864,RMVar_hsa_circ_187820,RMVar_hsa_circ_187819,RMVar_hsa_circ_187827,RMVar_hsa_circ_108393 101118 RMVar_ID_101118 Human_SNP_ID_634765929 m1A Human chr17 + 82036952 82036952 82036952 TCACCAGCAGGTCCACGGGGCCCACGCTGCCCAGCGCCCGCTCGGTGGCCTCCCAGTCACCCAGG TCACCAGCAGGTCCACGGGGCCCACGCTGCCCTGCGCCCGCTCGGTGGCCTCCCAGTCACCCAGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82036907..82037297 26863196 MeRIP-seq:(Medium) rs781252459 Functional Loss SNV dbSNP153 33..33 33 - - - 101119 RMVar_ID_101119 Human_SNP_ID_634766204 m1A Human chr17 + 82037570 82037570 82037570 CGCCCTATACCTGCCGGGAGCGGGCTCAGTGAAGGCGTCCCCTGCCCGCCTCTGCCCGCCGCCGG CGCCCTATACCTGCCGGGAGCGGGCTCAGTGAGGGCGTCCCCTGCCCGCCTCTGCCCGCCGCCGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82037551..82037700 26863196 MeRIP-seq:(Medium) rs1482164189 Functional Loss SNV dbSNP153 33..33 33 - - - 101120 RMVar_ID_101120 Human_SNP_ID_634771680 m1A Human chr17 + 82051596 82051596 82051596 CGGGTGGTCTTGACGGCGATGAAGACGTCGTCAGGCCGCAGGCTGGGGGCAGCGGGCCGGGACGG CGGGTGGTCTTGACGGCGATGAAGACGTCGTCTGGCCGCAGGCTGGGGGCAGCGGGCCGGGACGG A T GPS1 Ensembl:ENSG00000169727 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82051551..82051805 26863196 MeRIP-seq:(Medium) rs529961429 Functional Loss SNV dbSNP153 33..33 33 - - - 101121 RMVar_ID_101121 Human_SNP_ID_634771698 m1A Human chr17 + 82051625 82051625 82051625 GTCAGGCCGCAGGCTGGGGGCAGCGGGCCGGGACGGGGGCGCGCGCGGGGCCGGGGCGGGGGTCC GTCAGGCCGCAGGCTGGGGGCAGCGGGCCGGGCCGGGGGCGCGCGCGGGGCCGGGGCGGGGGTCC A C GPS1 Ensembl:ENSG00000169727 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82051621..82051747 26863196 MeRIP-seq:(Medium) rs1282102564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23257059 101122 RMVar_ID_101122 Human_SNP_ID_634771845 m1A Human chr17 - 82051966 82051966 82051966 GGCGCGGAGGCCCGGGGCGGCCTCGGCTCGTTACCTGCAAGTTAAACACCTGAACCGGCAGCGGC GGCGCGGAGGCCCGGGGCGGCCTCGGCTCGTTCCCTGCAAGTTAAACACCTGAACCGGCAGCGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:82051901..82052000 26863410 MeRIP-seq:(Medium) rs111627972 Functional Loss SNV dbSNP153 33..33 33 - - - 101123 RMVar_ID_101123 Human_SNP_ID_634772317 m1A Human chr17 + 82053128 82053128 82053128 GCCTGGGTGGGGGCGGGGGTGACTGGGAGGGCACACCTGGGGGACAGCAGCGGCGGGAGTGTGGT GCCTGGGTGGGGGCGGGGGTGACTGGGAGGGCGCACCTGGGGGACAGCAGCGGCGGGAGTGTGGT A G GPS1 Ensembl:ENSG00000169727 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82053117..82053301 26863196 MeRIP-seq:(Medium) rs1045987039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766041,Human_RBP_ID_822591,Human_RBP_ID_898103,Human_RBP_ID_1066740,Human_RBP_ID_3953310,Human_RBP_ID_5186017,Human_RBP_ID_8727326,Human_RBP_ID_9422643,Human_RBP_ID_18411942,Human_RBP_ID_18942497,Human_RBP_ID_18989682,Human_RBP_ID_19080625,Human_RBP_ID_21974855,Human_RBP_ID_22416298,Human_RBP_ID_22660741,Human_RBP_ID_22740759,Human_RBP_ID_27813240 RMVar_hsa_circ_88512,RMVar_hsa_circ_104069,RMVar_hsa_circ_187830,RMVar_hsa_circ_187831 101124 RMVar_ID_101124 Human_SNP_ID_634772418 m1A Human chr17 - 82053365 82053365 82053365 ACACCCAAGGTCCCCCCACTGGGCTCCGTACCAGGCTGGGGTTCTCCACCACGTAGTTGACGTCA ACACCCAAGGTCCCCCCACTGGGCTCCGTACCTGGCTGGGGTTCTCCACCACGTAGTTGACGTCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82053252..82053402 32194978 MeRIP-seq:(Medium) rs760149763 Functional Loss SNV dbSNP153 33..33 33 - - - 101125 RMVar_ID_101125 Human_SNP_ID_634772965 m1A Human chr17 + 82054658 82054658 82054658 ACACAGACCTGAAGAACTACAAGGGCAACTCCATCAAAGAGAGCATCCGGCGCGGCCACGACGAC ACACAGACCTGAAGAACTACAAGGGCAACTCCGTCAAAGAGAGCATCCGGCGCGGCCACGACGAC A G GPS1 Ensembl:ENSG00000169727 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82054607..82054730 26863196 MeRIP-seq:(Medium) rs1298801880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011203,Human_RBP_ID_1545404,Human_RBP_ID_1871130,Human_RBP_ID_13201812,Human_RBP_ID_18530988 RMVar_hsa_circ_1942,RMVar_hsa_circ_93786,RMVar_hsa_circ_88512,RMVar_hsa_circ_104069,RMVar_hsa_circ_187830,RMVar_hsa_circ_187831,RMVar_hsa_circ_8368,RMVar_hsa_circ_76197,RMVar_hsa_circ_17765,RMVar_hsa_circ_109678,RMVar_hsa_circ_187832,RMVar_hsa_circ_112668,RMVar_hsa_circ_187833,RMVar_hsa_circ_187834,RMVar_hsa_circ_187835 101126 RMVar_ID_101126 Human_SNP_ID_634773891 m1A Human chr17 + 82056759 82056759 82056759 GGAGGGGCTGATCAGTGCCCGTGTGGACTCACACAGCAAGGTGGCTGTGGGCTGCGGGGCGGTGG GGAGGGGCTGATCAGTGCCCGTGTGGACTCACGCAGCAAGGTGGCTGTGGGCTGCGGGGCGGTGG A G GPS1 Ensembl:ENSG00000169727 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82056631..82057237 26863196 MeRIP-seq:(Medium) rs1238606645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17903238 Human_Splice_Rec_1883915,Human_Splice_Rec_1883941,Human_Splice_Rec_1883965,Human_Splice_Rec_1884013,Human_Splice_Rec_1884075,Human_Splice_Rec_1884109,Human_Splice_Rec_1884133,Human_Splice_Rec_1884163,Human_Splice_Rec_1884183,Human_Splice_Rec_1884189,Human_Splice_Rec_1884193 RMVar_hsa_circ_93786,RMVar_hsa_circ_104069,RMVar_hsa_circ_187831,RMVar_hsa_circ_187832,RMVar_hsa_circ_112668,RMVar_hsa_circ_187834,RMVar_hsa_circ_91268,RMVar_hsa_circ_101739,RMVar_hsa_circ_187836,RMVar_hsa_circ_106850,RMVar_hsa_circ_187838,RMVar_hsa_circ_90754,RMVar_hsa_circ_49044,RMVar_hsa_circ_87744,RMVar_hsa_circ_187839,RMVar_hsa_circ_187840,RMVar_hsa_circ_187841,RMVar_hsa_circ_108077,RMVar_hsa_circ_346847,RMVar_hsa_circ_187843,RMVar_hsa_circ_187844 101127 RMVar_ID_101127 Human_SNP_ID_634774482 m1A Human chr17 + 82058127 82058127 82058127 GGGGTGGGGGTTGTGGGCCTTCAGGCCAGGGCACTGCCCATGACTTCGGAGAAGCCACCTGGTGT GGGGTGGGGGTTGTGGGCCTTCAGGCCAGGGCGCTGCCCATGACTTCGGAGAAGCCACCTGGTGT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82058076..82058200 32194978 MeRIP-seq:(Medium) rs749210269 Functional Loss SNV dbSNP153 33..33 33 - - - 101128 RMVar_ID_101128 Human_SNP_ID_634775251 m1A Human chr17 + 82059986 82059986 82059986 GAGAGGGGTCGAAGGTCTTGTGGGGGTTCCTCAGCTGCTTCTTTTGCTTGTTCTTGGACAGGACC GAGAGGGGTCGAAGGTCTTGTGGGGGTTCCTCTGCTGCTTCTTTTGCTTGTTCTTGGACAGGACC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82059976..82060025 26863196 MeRIP-seq:(Medium) rs1415191097 Functional Loss SNV dbSNP153 33..33 33 - - - 101129 RMVar_ID_101129 Human_SNP_ID_634775260 m1A Human chr17 - 82060008 82060008 82060008 AGGAAGAGGAGGGTGGCACGGAGGTCCTGTCCAAGAACAAGCAAAAGAAGCAGCTGAGGAACCCC AGGAAGAGGAGGGTGGCACGGAGGTCCTGTCCGAGAACAAGCAAAAGAAGCAGCTGAGGAACCCC T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82059926..82060144 26863196 MeRIP-seq:(Medium) rs1180549991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48933,Human_RBP_ID_503388,Human_RBP_ID_897120,Human_RBP_ID_3951444,Human_RBP_ID_4460965,Human_RBP_ID_6652746,Human_RBP_ID_8466610,Human_RBP_ID_9377159,Human_RBP_ID_18993040,Human_RBP_ID_22224287,Human_RBP_ID_22958468,Human_RBP_ID_23755559,Human_RBP_ID_26332611,Human_RBP_ID_26975405,Human_RBP_ID_27814398 Human_Splice_Rec_1884212,Human_Splice_Rec_1884213,Human_Splice_Rec_1884234,Human_Splice_Rec_1884235,Human_Splice_Rec_1884241,Human_Splice_Rec_1884262,Human_Splice_Rec_1884263,Human_Splice_Rec_1884269,Human_Splice_Rec_1884276,Human_Splice_Rec_1884277,Human_Splice_Rec_1884292,Human_Splice_Rec_1884293,Human_Splice_Rec_1884297 RMVar_hsa_circ_80373,RMVar_hsa_circ_187845 101130 RMVar_ID_101130 Human_SNP_ID_634775310 m1A Human chr17 - 82060089 82060089 82060089 TGGGCTCTGCCCGCTGCCCTCCCCTCAGGCCCAGGGAGGGGAGCAAGGAGAAGGCAGGTGCGCGC TGGGCTCTGCCCGCTGCCCTCCCCTCAGGCCCGGGGAGGGGAGCAAGGAGAAGGCAGGTGCGCGC T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82060040..82060191 32194978 MeRIP-seq:(Medium) rs766102627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822066,Human_RBP_ID_898950,Human_RBP_ID_3951445,Human_RBP_ID_5365599,Human_RBP_ID_9377160,Human_RBP_ID_22657100 Human_Splice_Rec_1884212,Human_Splice_Rec_1884234,Human_Splice_Rec_1884262,Human_Splice_Rec_1884276,Human_Splice_Rec_1884292 RMVar_hsa_circ_80373,RMVar_hsa_circ_187845 101131 RMVar_ID_101131 Human_SNP_ID_634775903 m1A Human chr17 - 82061565 82061565 82061565 CAGCCAGGGCCCCATGCACACGGCCTGATACCACCGCCCAGGTCGGTGCCTCCCACTGCCTACTG CAGCCAGGGCCCCATGCACACGGCCTGATACCTCCGCCCAGGTCGGTGCCTCCCACTGCCTACTG T A DUS1L Ensembl:ENSG00000169718 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82061558..82061643 26863196 MeRIP-seq:(Medium) rs1391529584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19080649 Human_Splice_Rec_1884285,Human_Splice_Rec_1884341 RMVar_hsa_circ_80373,RMVar_hsa_circ_187845,RMVar_hsa_circ_126795,RMVar_hsa_circ_187846 101132 RMVar_ID_101132 Human_SNP_ID_634776068 m1A Human chr17 - 82061955 82061955 82061955 CTAGTTGCTGACGGTGCACGGACGCACCAAGGAGCAGAAGGGGCCCCTGTCGGGTGCAGCGTCCT CTAGTTGCTGACGGTGCACGGACGCACCAAGGGGCAGAAGGGGCCCCTGTCGGGTGCAGCGTCCT T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82061870..82062006 26863196 MeRIP-seq:(Medium) rs1462574566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236666,Human_RBP_ID_262858,Human_RBP_ID_503396,Human_RBP_ID_901218,Human_RBP_ID_3951451,Human_RBP_ID_4461004,Human_RBP_ID_18989705,Human_RBP_ID_19080650 Human_Splice_Rec_1884204,Human_Splice_Rec_1884205,Human_Splice_Rec_1884226,Human_Splice_Rec_1884227,Human_Splice_Rec_1884248,Human_Splice_Rec_1884249,Human_Splice_Rec_1884254,Human_Splice_Rec_1884255,Human_Splice_Rec_1884306,Human_Splice_Rec_1884307,Human_Splice_Rec_1884322,Human_Splice_Rec_1884323,Human_Splice_Rec_1884338,Human_Splice_Rec_1884339,Human_Splice_Rec_1884350,Human_Splice_Rec_1884351 RMVar_hsa_circ_80373,RMVar_hsa_circ_187845,RMVar_hsa_circ_126795,RMVar_hsa_circ_187846 101133 RMVar_ID_101133 Human_SNP_ID_634777078 m1A Human chr17 - 82065054 82065054 82065054 CTGCGCCTTTCCCCCAGCCTGGAGACGATGCCAAAGCTGCAGGGCTTCGAGTTCTGGAGCCGCAC CTGCGCCTTTCCCCCAGCCTGGAGACGATGCCGAAGCTGCAGGGCTTCGAGTTCTGGAGCCGCAC T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82064797..82065094 26863196 MeRIP-seq:(Medium) rs892746494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503410,Human_RBP_ID_1545470,Human_RBP_ID_4464971,Human_RBP_ID_18712160 Human_Splice_Rec_1884196,Human_Splice_Rec_1884314,Human_Splice_Rec_1884330,Human_Splice_Rec_1884344,Human_Splice_Rec_1884356 Human_miRNA_ID_2013839,Human_miRNA_ID_2381419,Human_miRNA_ID_2760237,Human_miRNA_ID_3024429 RMVar_hsa_circ_7198,RMVar_hsa_circ_126795,RMVar_hsa_circ_187846 101134 RMVar_ID_101134 Human_SNP_ID_634777296 m1A Human chr17 - 82065725 82065707 82065725 CGGCGCGGTGCGGGCGTTCGCGGCGCCCCGGGAGCTGCAGGGGCCCCGGGCGGCGGCGAGGCCGG CGGCGCGGTGCGGGCGTTCGCGGCGCCCCGGG__________________CGGCGGCGAGGCCGG GCCCGGGGCCCCTGCAGCT G DUS1L Ensembl:ENSG00000169718 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type chr17:82065676..82065750;chr17:82065626..82065800 26863196,26863410 MeRIP-seq:(Medium) rs1261786530 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_238077,Human_RBP_ID_768655,Human_RBP_ID_4464972,Human_RBP_ID_5526082,Human_RBP_ID_8825089,Human_RBP_ID_17126848 101135 RMVar_ID_101135 Human_SNP_ID_634777303 m1A Human chr17 - 82065719 82065719 82065719 GGTGCGGGCGTTCGCGGCGCCCCGGGAGCTGCAGGGGCCCCGGGCGGCGGCGAGGCCGGAGAGGG GGTGCGGGCGTTCGCGGCGCCCCGGGAGCTGCGGGGGCCCCGGGCGGCGGCGAGGCCGGAGAGGG T C DUS1L Ensembl:ENSG00000169718 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:82065587..82065800 26863410 MeRIP-seq:(Medium) rs1381655917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238077,Human_RBP_ID_768655,Human_RBP_ID_4464972,Human_RBP_ID_5526082,Human_RBP_ID_8825089,Human_RBP_ID_17126848 101136 RMVar_ID_101136 Human_SNP_ID_634777305 m1A Human chr17 + 82065722 82065722 82065722 TCTCCGGCCTCGCCGCCGCCCGGGGCCCCTGCAGCTCCCGGGGCGCCGCGAACGCCCGCACCGCG TCTCCGGCCTCGCCGCCGCCCGGGGCCCCTGCCGCTCCCGGGGCGCCGCGAACGCCCGCACCGCG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:82065625..82065800 26863410 MeRIP-seq:(Medium) rs548163681 Functional Loss SNV dbSNP153 33..33 33 - - - 101137 RMVar_ID_101137 Human_SNP_ID_634781292 m1A Human chr17 - 82078821 82078821 82078821 TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCATATTTATTGCATTGCTGGTAGAGACCCCCAGG TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCTTATTTATTGCATTGCTGGTAGAGACCCCCAGG T A FASN Ensembl:ENSG00000169710 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82078801..82078825 26863196 MeRIP-seq:(Medium) rs548589236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301462,Human_RBP_ID_503429 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 101138 RMVar_ID_101138 Human_SNP_ID_634781293 m1A Human chr17 - 82078821 82078821 82078821 TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCATATTTATTGCATTGCTGGTAGAGACCCCCAGG TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCGTATTTATTGCATTGCTGGTAGAGACCCCCAGG T C FASN Ensembl:ENSG00000169710 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82078801..82078825 26863196 MeRIP-seq:(Medium) rs548589236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301462,Human_RBP_ID_503429 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 101139 RMVar_ID_101139 Human_SNP_ID_634781480 m1A Human chr17 - 82079273 82079273 82079273 CGGCAGCTGATCGCATCCCCTGCAGGTATGCGACGGGAAAGTATCCGTCCACGTCATCGAGGGTG CGGCAGCTGATCGCATCCCCTGCAGGTATGCGGCGGGAAAGTATCCGTCCACGTCATCGAGGGTG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82079226..82079275 26863196 MeRIP-seq:(Medium) rs866060714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1884446,Human_Splice_Rec_1884530,Human_Splice_Rec_1884532,Human_Splice_Rec_1884538,Human_Splice_Rec_1884546,Human_Splice_Rec_1884548 Human_miRNA_ID_2135176 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 101140 RMVar_ID_101140 Human_SNP_ID_634781528 m1A Human chr17 - 82079358 82079358 82079358 CGAGGACCTGGGCGCGGACTACAACCTCTCCCAGGTGCGCAAGGGGCCTGACGGGAACGGGGACA CGAGGACCTGGGCGCGGACTACAACCTCTCCCTGGTGCGCAAGGGGCCTGACGGGAACGGGGACA T A FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82079351..82079375 26863196 MeRIP-seq:(Medium) rs1325108382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084695 Human_Splice_Rec_1884445,Human_Splice_Rec_1884529,Human_Splice_Rec_1884531,Human_Splice_Rec_1884537,Human_Splice_Rec_1884545,Human_Splice_Rec_1884547 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 101141 RMVar_ID_101141 Human_SNP_ID_634781529 m1A Human chr17 - 82079358 82079358 82079358 CGAGGACCTGGGCGCGGACTACAACCTCTCCCAGGTGCGCAAGGGGCCTGACGGGAACGGGGACA CGAGGACCTGGGCGCGGACTACAACCTCTCCCGGGTGCGCAAGGGGCCTGACGGGAACGGGGACA T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82079351..82079375 26863196 MeRIP-seq:(Medium) rs1325108382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19084695 Human_Splice_Rec_1884445,Human_Splice_Rec_1884529,Human_Splice_Rec_1884531,Human_Splice_Rec_1884537,Human_Splice_Rec_1884545,Human_Splice_Rec_1884547 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 101142 RMVar_ID_101142 Human_SNP_ID_634782100 m1A Human chr17 - 82080725 82080725 82080725 CCACCGTGTTCCACAGCCTGGCCTCCCGGCTCAGCATCCCCACCTATGGCCTGCAGTGCACCCGA CCACCGTGTTCCACAGCCTGGCCTCCCGGCTCCGCATCCCCACCTATGGCCTGCAGTGCACCCGA T G FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr17:82080701..82080775;chr17:82080551..82080770 26863196 MeRIP-seq:(Medium) rs1416922343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503450,Human_RBP_ID_766004,Human_RBP_ID_8466645,Human_RBP_ID_8823672,Human_RBP_ID_9258087,Human_RBP_ID_18191080 Human_Splice_Rec_1884439,Human_Splice_Rec_1884523,Human_Splice_Rec_1884539 Human_miRNA_ID_2726511 RMVar_hsa_circ_100717,RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187860 101143 RMVar_ID_101143 Human_SNP_ID_634782303 m1A Human chr17 + 82081190 82081190 82081190 ACGCACCGCTGGCCTCATCCGCCTTTGAGGACAGCTCCTGCAGTTTCCGGAGCGTGAGTTGCCGC ACGCACCGCTGGCCTCATCCGCCTTTGAGGACGGCTCCTGCAGTTTCCGGAGCGTGAGTTGCCGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82081176..82081200 26863196 MeRIP-seq:(Medium) rs770973786 Functional Loss SNV dbSNP153 33..33 33 - - - 101144 RMVar_ID_101144 Human_SNP_ID_634782528 m1A Human chr17 - 82081697 82081697 82081697 AGGTGCTGGACCTCTTCCTGAACCAGCCCCACATGGTCCTGAGCAGCTTTGTGCTGGCTGAGAAG AGGTGCTGGACCTCTTCCTGAACCAGCCCCACGTGGTCCTGAGCAGCTTTGTGCTGGCTGAGAAG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82081647..82081867 26863196 MeRIP-seq:(Medium) rs1356589443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503453,Human_RBP_ID_1871182,Human_RBP_ID_4461146,Human_RBP_ID_8823687,Human_RBP_ID_22500823 Human_Splice_Rec_1884435,Human_Splice_Rec_1884519 Human_miRNA_ID_2297848,Human_miRNA_ID_2407384,Human_miRNA_ID_2410379,Human_miRNA_ID_2413359 RMVar_hsa_circ_100717,RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187860 101145 RMVar_ID_101145 Human_SNP_ID_634782584 m1A Human chr17 - 82081805 82081805 82081805 CCGTGCAGTGGGGCGCCATCGGCGACGTGGGCATTTTGGTGGAGACGATGAGCACCAACGACACG CCGTGCAGTGGGGCGCCATCGGCGACGTGGGCGTTTTGGTGGAGACGATGAGCACCAACGACACG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82081758..82081849 26863196 MeRIP-seq:(Medium) rs946823999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4481282,Human_RBP_ID_6652795,Human_RBP_ID_8823694,Human_RBP_ID_17693387,Human_RBP_ID_17903270,Human_RBP_ID_18297156,Human_RBP_ID_22959309,Human_RBP_ID_26975496 Human_Splice_Rec_1884434,Human_Splice_Rec_1884518 Human_miRNA_ID_2496713,Human_miRNA_ID_2497939 RMVar_hsa_circ_100717,RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187860 101146 RMVar_ID_101146 Human_SNP_ID_634782992 m1A Human chr17 - 82082602 82082602 82082602 CAGGTGCAGGTGTCCACCAGCAACATCAGCTCACTGGAGGGGGCCCGGGGCCTCATTGCCGAGGC CAGGTGCAGGTGTCCACCAGCAACATCAGCTCCCTGGAGGGGGCCCGGGGCCTCATTGCCGAGGC T G FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82082551..82082625 26863196 MeRIP-seq:(Medium) rs1181456960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48904,Human_RBP_ID_1545489,Human_RBP_ID_5237783,Human_RBP_ID_6666617,Human_RBP_ID_8823705 Human_Splice_Rec_1884428,Human_Splice_Rec_1884429,Human_Splice_Rec_1884512,Human_Splice_Rec_1884513 Human_miRNA_ID_2296191 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187855,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_96042,RMVar_hsa_circ_187863 101147 RMVar_ID_101147 Human_SNP_ID_634783030 m1A Human chr17 + 82082676 82082676 82082676 GCGCCTCCACCGGCGGACCTGCTTGGCCTGGTAGCCTGCGGGACACAGGACTGTGGGCTGGACTG GCGCCTCCACCGGCGGACCTGCTTGGCCTGGTCGCCTGCGGGACACAGGACTGTGGGCTGGACTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82082513..82082712 26863196 MeRIP-seq:(Medium) rs374709802 Functional Loss SNV dbSNP153 33..33 33 - - - 101148 RMVar_ID_101148 Human_SNP_ID_634783541 m1A Human chr17 - 82083756 82083747 82083756 GCACACGGGCGGGAAGGGTGAGTGGCCCCCACAGCCCCCACCTGCCTCCTGCCTAGCCTCCGGCC GCACACGGGCGGGAAGGGTGAGTGGCCCCCAC_________CTGCCTCCTGCCTAGCCTCCGGCC GGTGGGGGCT G FASN Ensembl:ENSG00000169710 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82083749..82084405 26863196 MeRIP-seq:(Medium) rs760726858 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_19080681 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_113795,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_38236,RMVar_hsa_circ_40175,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_96042,RMVar_hsa_circ_101410,RMVar_hsa_circ_187863,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_125712,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_105440,RMVar_hsa_circ_187868,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_187867 101149 RMVar_ID_101149 Human_SNP_ID_634783555 m1A Human chr17 - 82083756 82083756 82083756 GCACACGGGCGGGAAGGGTGAGTGGCCCCCACAGCCCCCACCTGCCTCCTGCCTAGCCTCCGGCC GCACACGGGCGGGAAGGGTGAGTGGCCCCCACGGCCCCCACCTGCCTCCTGCCTAGCCTCCGGCC T C FASN Ensembl:ENSG00000169710 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82083749..82084405 26863196 MeRIP-seq:(Medium) rs1183862157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19080681 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_113795,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_38236,RMVar_hsa_circ_40175,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_96042,RMVar_hsa_circ_101410,RMVar_hsa_circ_187863,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_125712,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_105440,RMVar_hsa_circ_187868,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_187867 101150 RMVar_ID_101150 Human_SNP_ID_634783600 m1A Human chr17 - 82083870 82083870 82083870 CTCTTCACCAGGGTCGGCTGAGAAGCGGGCGTACCTCCAGGCCAGGTTCCCCCAGCTCGACAGCA CTCTTCACCAGGGTCGGCTGAGAAGCGGGCGTGCCTCCAGGCCAGGTTCCCCCAGCTCGACAGCA T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82081659..82085139 32194978 MeRIP-seq:(Medium) rs762078680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3953356,Human_RBP_ID_4461211,Human_RBP_ID_5368685,Human_RBP_ID_8823735,Human_RBP_ID_17494633,Human_RBP_ID_18191431 Human_Splice_Rec_1884420,Human_Splice_Rec_1884421,Human_Splice_Rec_1884504,Human_Splice_Rec_1884505 Human_miRNA_ID_2724305,Human_miRNA_ID_2946272 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_113795,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_38236,RMVar_hsa_circ_40175,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_96042,RMVar_hsa_circ_101410,RMVar_hsa_circ_187863,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_125712,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_105440,RMVar_hsa_circ_187868,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_187867 101151 RMVar_ID_101151 Human_SNP_ID_634783972 m1A Human chr17 - 82084596 82084596 82084596 GCGCCATGCCCAGCCCACCTGCCCTGGCGCCCAGCTCTGCACGGTCTACTACGCCTCCCTCAACT GCGCCATGCCCAGCCCACCTGCCCTGGCGCCCCGCTCTGCACGGTCTACTACGCCTCCCTCAACT T G FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82084551..82084625 26863196 MeRIP-seq:(Medium) rs752553190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652825,Human_RBP_ID_8466659,Human_RBP_ID_8823749,Human_RBP_ID_17494637,Human_RBP_ID_18191095,Human_RBP_ID_22807502 Human_Splice_Rec_1884415,Human_Splice_Rec_1884499 Human_miRNA_ID_2585369 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_96042,RMVar_hsa_circ_101410,RMVar_hsa_circ_187863,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_125712,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_105440,RMVar_hsa_circ_187868,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_187867,RMVar_hsa_circ_105832,RMVar_hsa_circ_264990,RMVar_hsa_circ_328132,RMVar_hsa_circ_187871,RMVar_hsa_circ_348221 101152 RMVar_ID_101152 Human_SNP_ID_634784194 m1A Human chr17 + 82085005 82085005 82085005 GCTCAGGCTGGGGATGGGGAGGCTGGTGGGGAAGGGGAAGTGGTGAGGGGCCGTGCTCCTACCGG GCTCAGGCTGGGGATGGGGAGGCTGGTGGGGATGGGGAAGTGGTGAGGGGCCGTGCTCCTACCGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82085001..82085050 26863196 MeRIP-seq:(Medium) rs1384818213 Functional Loss SNV dbSNP153 33..33 33 - - - 101153 RMVar_ID_101153 Human_SNP_ID_634784504 m1A Human chr17 + 82085528 82085528 82085528 CCTGGCCATACTGCGGCTCAGTGGAGGTGAGGAAGGCCACGATGTCCCCGAGGGGGTGCCCCCGG CCTGGCCATACTGCGGCTCAGTGGAGGTGAGGGAGGCCACGATGTCCCCGAGGGGGTGCCCCCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82085401..82085729 26863196 MeRIP-seq:(Medium) rs1269269475 Functional Loss SNV dbSNP153 33..33 33 - - - 101154 RMVar_ID_101154 Human_SNP_ID_634785227 m1A Human chr17 - 82087182 82087182 82087182 TGGCCGGAGGCGTCCACATCTCCGGGCTCCACACTGAGTCGGCCCCGCGGCGGCAGCAGGAGCAG TGGCCGGAGGCGTCCACATCTCCGGGCTCCACGCTGAGTCGGCCCCGCGGCGGCAGCAGGAGCAG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82087028..82087508 26863196 MeRIP-seq:(Medium) rs889803121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48916,Human_RBP_ID_903923,Human_RBP_ID_1871202,Human_RBP_ID_4481329,Human_RBP_ID_8823790,Human_RBP_ID_9288526,Human_RBP_ID_18191447,Human_RBP_ID_19080686,Human_RBP_ID_22587255,Human_RBP_ID_22659628,Human_RBP_ID_23257069,Human_RBP_ID_27459255 Human_Splice_Rec_1884402,Human_Splice_Rec_1884486 Human_miRNA_ID_3066304 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_21577,RMVar_hsa_circ_79716,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_105832,RMVar_hsa_circ_264990,RMVar_hsa_circ_187871,RMVar_hsa_circ_113373,RMVar_hsa_circ_187872,RMVar_hsa_circ_104196,RMVar_hsa_circ_187873,RMVar_hsa_circ_187874,RMVar_hsa_circ_96532,RMVar_hsa_circ_187877 101155 RMVar_ID_101155 Human_SNP_ID_634785795 m1A Human chr17 - 82088302 82088302 82088302 TGTGCTGAGGCCTGTGCCCTCCCGCAGACACCAGCTCCGAGTCTCCTGACCACTACCTGGTGGAC TGTGCTGAGGCCTGTGCCCTCCCGCAGACACCGGCTCCGAGTCTCCTGACCACTACCTGGTGGAC T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82088217..82088403 26863196 MeRIP-seq:(Medium) rs1411951907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2526623,Human_RBP_ID_5187851,Human_RBP_ID_8823814,Human_RBP_ID_22658080 Human_Splice_Rec_1884394,Human_Splice_Rec_1884478 Human_miRNA_ID_2052595 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_264990,RMVar_hsa_circ_113373,RMVar_hsa_circ_187874,RMVar_hsa_circ_79649,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_187879 101156 RMVar_ID_101156 Human_SNP_ID_634785852 m1A Human chr17 - 82088393 82088393 82088393 GTTCAGGTTCCCCCTCAGCCGCCATCTACAACATCGGTGAGCAGGGGCCCGGCGGGTGGGCAGAC GTTCAGGTTCCCCCTCAGCCGCCATCTACAACGTCGGTGAGCAGGGGCCCGGCGGGTGGGCAGAC T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:82087693..82088577;chr17:82088176..82088575 26863196 MeRIP-seq:(Medium) rs950933290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17494650,Human_RBP_ID_17903301,Human_RBP_ID_18191108,Human_RBP_ID_19084729,Human_RBP_ID_26975581,Human_RBP_ID_27262951 Human_Splice_Rec_1884393,Human_Splice_Rec_1884477 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_113373,RMVar_hsa_circ_187874,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_374345,RMVar_hsa_circ_110707,RMVar_hsa_circ_187881,RMVar_hsa_circ_187882 101157 RMVar_ID_101157 Human_SNP_ID_634785865 m1A Human chr17 - 82088421 82088421 82088421 GTGCCGGCCGCCGAGGACTTCCCCAACGGTTCAGGTTCCCCCTCAGCCGCCATCTACAACATCGG GTGCCGGCCGCCGAGGACTTCCCCAACGGTTCTGGTTCCCCCTCAGCCGCCATCTACAACATCGG T A FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82087951..82088586 26863196 MeRIP-seq:(Medium) rs746606873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3539979,Human_RBP_ID_8823815,Human_RBP_ID_17262474,Human_RBP_ID_17494650,Human_RBP_ID_18712226,Human_RBP_ID_22224413 Human_Splice_Rec_1884393,Human_Splice_Rec_1884477 Human_miRNA_ID_2946273 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_113373,RMVar_hsa_circ_187874,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_374345,RMVar_hsa_circ_110707,RMVar_hsa_circ_187881,RMVar_hsa_circ_187882 101158 RMVar_ID_101158 Human_SNP_ID_634785866 m1A Human chr17 - 82088421 82088421 82088421 GTGCCGGCCGCCGAGGACTTCCCCAACGGTTCAGGTTCCCCCTCAGCCGCCATCTACAACATCGG GTGCCGGCCGCCGAGGACTTCCCCAACGGTTCGGGTTCCCCCTCAGCCGCCATCTACAACATCGG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82087951..82088586 26863196 MeRIP-seq:(Medium) rs746606873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3539979,Human_RBP_ID_8823815,Human_RBP_ID_17262474,Human_RBP_ID_17494650,Human_RBP_ID_18712226,Human_RBP_ID_22224413 Human_Splice_Rec_1884393,Human_Splice_Rec_1884477 Human_miRNA_ID_2946273 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_113373,RMVar_hsa_circ_187874,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_374345,RMVar_hsa_circ_110707,RMVar_hsa_circ_187881,RMVar_hsa_circ_187882 101159 RMVar_ID_101159 Human_SNP_ID_634786010 m1A Human chr17 + 82088755 82088755 82088755 ACTCCGGGAGACGAGACCCGGGCTGGGAAGGGACCCACCCTGAGAGGTGCAGCCTGCCGATGCCG ACTCCGGGAGACGAGACCCGGGCTGGGAAGGGTCCCACCCTGAGAGGTGCAGCCTGCCGATGCCG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82088751..82088800 26863196 MeRIP-seq:(Medium) rs879155268 Functional Loss SNV dbSNP153 33..33 33 - - - 101160 RMVar_ID_101160 Human_SNP_ID_634786175 m1A Human chr17 - 82089088 82089088 82089088 CCGAGGCCCAGTGGCACAGCAGCCTGGCACGCACGTCCTCCGCCGAGTACAATGTCAACAACCTG CCGAGGCCCAGTGGCACAGCAGCCTGGCACGCGCGTCCTCCGCCGAGTACAATGTCAACAACCTG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82089040..82089106 26863196 MeRIP-seq:(Medium) rs775293139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48921,Human_RBP_ID_6652862,Human_RBP_ID_22807517 Human_Splice_Rec_1884388,Human_Splice_Rec_1884472 Human_miRNA_ID_2018021 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_113373,RMVar_hsa_circ_187874,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_110707,RMVar_hsa_circ_84556,RMVar_hsa_circ_109027,RMVar_hsa_circ_187882,RMVar_hsa_circ_86903,RMVar_hsa_circ_12041,RMVar_hsa_circ_187883,RMVar_hsa_circ_187884,RMVar_hsa_circ_187885,RMVar_hsa_circ_100656,RMVar_hsa_circ_187886 101161 RMVar_ID_101161 Human_SNP_ID_634787211 m1A Human chr17 + 82091463 82091463 82091463 CCGCTGGCCCGCAGCAGACGGGGCAGGGTGGCATGTGGGGCGGGTGCGGGGGGCGGCTGCGTGTT CCGCTGGCCCGCAGCAGACGGGGCAGGGTGGCTTGTGGGGCGGGTGCGGGGGGCGGCTGCGTGTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82091208..82091674 26863196 MeRIP-seq:(Medium) rs1379538388 Functional Loss SNV dbSNP153 33..33 33 - - - 101162 RMVar_ID_101162 Human_SNP_ID_634787238 m1A Human chr17 - 82091501 82091501 82091501 GCTTCGGGGGCTCCAACGTGCACATCATCCTGAGGCCCAACACGCAGCCGCCCCCCGCACCCGCC GCTTCGGGGGCTCCAACGTGCACATCATCCTGGGGCCCAACACGCAGCCGCCCCCCGCACCCGCC T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82091476..82091500 26863196 MeRIP-seq:(Medium) rs780441119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48925,Human_RBP_ID_1011244,Human_RBP_ID_22532935,Human_RBP_ID_22807526,Human_RBP_ID_27459283 Clinvar_Rec_619 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_84556,RMVar_hsa_circ_109027,RMVar_hsa_circ_86903,RMVar_hsa_circ_187883,RMVar_hsa_circ_187884,RMVar_hsa_circ_187885,RMVar_hsa_circ_100656,RMVar_hsa_circ_106866,RMVar_hsa_circ_187886,RMVar_hsa_circ_187887,RMVar_hsa_circ_75275,RMVar_hsa_circ_102666,RMVar_hsa_circ_110978,RMVar_hsa_circ_375910,RMVar_hsa_circ_7784,RMVar_hsa_circ_119342,RMVar_hsa_circ_187889,RMVar_hsa_circ_187891,RMVar_hsa_circ_187893,RMVar_hsa_circ_94700,RMVar_hsa_circ_187892,RMVar_hsa_circ_187890,RMVar_hsa_circ_126768,RMVar_hsa_circ_187895 101163 RMVar_ID_101163 Human_SNP_ID_634787301 m1A Human chr17 - 82091647 82091647 82091647 GCTGTCCCTGGAGCACGGGCTCTGGGCCCCCAACCTGCACTTCCATAGCCCCAACCCTGAGATCC GCTGTCCCTGGAGCACGGGCTCTGGGCCCCCAGCCTGCACTTCCATAGCCCCAACCCTGAGATCC T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:82091626..82091650;chr17:82091601..82091700 26863196 MeRIP-seq:(Medium) rs1296646858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5363339,Human_RBP_ID_8823859,Human_RBP_ID_18712248,Human_RBP_ID_19080708,Human_RBP_ID_22060583,Human_RBP_ID_22659646,Human_RBP_ID_26975630,Human_RBP_ID_27459287 Human_Splice_Rec_1884378,Human_Splice_Rec_1884462 Human_miRNA_ID_2806562,Human_miRNA_ID_2809706,Human_miRNA_ID_2812847 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187865,RMVar_hsa_circ_21577,RMVar_hsa_circ_187870,RMVar_hsa_circ_22589,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_84556,RMVar_hsa_circ_109027,RMVar_hsa_circ_86903,RMVar_hsa_circ_187883,RMVar_hsa_circ_187884,RMVar_hsa_circ_187885,RMVar_hsa_circ_100656,RMVar_hsa_circ_106866,RMVar_hsa_circ_187886,RMVar_hsa_circ_187887,RMVar_hsa_circ_75275,RMVar_hsa_circ_102666,RMVar_hsa_circ_110978,RMVar_hsa_circ_375910,RMVar_hsa_circ_7784,RMVar_hsa_circ_119342,RMVar_hsa_circ_187889,RMVar_hsa_circ_187891,RMVar_hsa_circ_187893,RMVar_hsa_circ_94700,RMVar_hsa_circ_187892,RMVar_hsa_circ_187890,RMVar_hsa_circ_126768,RMVar_hsa_circ_187895 101164 RMVar_ID_101164 Human_SNP_ID_634788207 m1A Human chr17 - 82093674 82093674 82093674 ACCTCGGAGGCCCTGAGCCGAGACCCCGAGACACTCGTGGGCTACAGCATGGTGGGCTGCCAGCG ACCTCGGAGGCCCTGAGCCGAGACCCCGAGACGCTCGTGGGCTACAGCATGGTGGGCTGCCAGCG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82093623..82093756 26863196 MeRIP-seq:(Medium) rs767487369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8823871,Human_RBP_ID_9327609,Human_RBP_ID_22961868 Human_Splice_Rec_1884368,Human_Splice_Rec_1884369,Human_Splice_Rec_1884452,Human_Splice_Rec_1884453,Human_Splice_Rec_1884556 RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_21577,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_109027,RMVar_hsa_circ_86903,RMVar_hsa_circ_187884,RMVar_hsa_circ_187885,RMVar_hsa_circ_21378,RMVar_hsa_circ_110978,RMVar_hsa_circ_7784,RMVar_hsa_circ_119342,RMVar_hsa_circ_187889,RMVar_hsa_circ_187890,RMVar_hsa_circ_47950,RMVar_hsa_circ_121912,RMVar_hsa_circ_187898 101165 RMVar_ID_101165 Human_SNP_ID_634788236 m1A Human chr17 - 82093739 82093739 82093739 GCATCAACCCAGATTCACTCCGAGGAACACACACTGGCGTCTGGGTGGGCGTGAGCGGCTCTGAG GCATCAACCCAGATTCACTCCGAGGAACACACGCTGGCGTCTGGGTGGGCGTGAGCGGCTCTGAG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82093608..82093801 26863196 MeRIP-seq:(Medium) rs753896526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503471,Human_RBP_ID_3539988,Human_RBP_ID_4481390,Human_RBP_ID_6652884,Human_RBP_ID_8823875,Human_RBP_ID_13201899,Human_RBP_ID_17903316,Human_RBP_ID_18439920,Human_RBP_ID_22224449,Human_RBP_ID_22657141,Human_RBP_ID_25331794,Human_RBP_ID_27156992 Human_Splice_Rec_1884368,Human_Splice_Rec_1884452,Human_Splice_Rec_1884556 Human_miRNA_ID_2175761,Human_miRNA_ID_2179205 RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_187849,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_21577,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_109027,RMVar_hsa_circ_86903,RMVar_hsa_circ_187884,RMVar_hsa_circ_187885,RMVar_hsa_circ_21378,RMVar_hsa_circ_110978,RMVar_hsa_circ_7784,RMVar_hsa_circ_119342,RMVar_hsa_circ_187889,RMVar_hsa_circ_187890,RMVar_hsa_circ_47950,RMVar_hsa_circ_121912,RMVar_hsa_circ_187898 101166 RMVar_ID_101166 Human_SNP_ID_634788744 m1A Human chr17 - 82095033 82095033 82095033 CTGGTGCTGGGGCCGGGGCCGGGGCTGGAGTGACGAGAGGCAAAGCAGGAGGTTCTTGAGGGGCC CTGGTGCTGGGGCCGGGGCCGGGGCTGGAGTGGCGAGAGGCAAAGCAGGAGGTTCTTGAGGGGCC T C FASN Ensembl:ENSG00000169710 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82095031..82095119 26863196 MeRIP-seq:(Medium) rs1017162771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13201948,Human_RBP_ID_22587269,Human_RBP_ID_26781332,Human_RBP_ID_26975674 RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_89138,RMVar_hsa_circ_187878,RMVar_hsa_circ_86903,RMVar_hsa_circ_187885,RMVar_hsa_circ_110978,RMVar_hsa_circ_7784,RMVar_hsa_circ_119342,RMVar_hsa_circ_187889,RMVar_hsa_circ_187890,RMVar_hsa_circ_47950,RMVar_hsa_circ_121912,RMVar_hsa_circ_187898 101167 RMVar_ID_101167 Human_SNP_ID_634789770 m1A Human chr17 + 82097812 82097812 82097812 GAGGATGCGGCGGCGCCTTTGTGGGCGCGGGGAGGCCGAGCCGGGGGCTCCTCCAGGCCCTTCAG GAGGATGCGGCGGCGCCTTTGTGGGCGCGGGGCGGCCGAGCCGGGGGCTCCTCCAGGCCCTTCAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82097801..82097875 26863196 MeRIP-seq:(Medium) rs1439035961 Functional Loss SNV dbSNP153 33..33 33 - - - 101168 RMVar_ID_101168 Human_SNP_ID_634789892 m1A Human chr17 - 82098188 82098188 82098188 AGCGGCCCCGGCCTCCCTCTCCGCCGCGCTTCAGCCTCCCGCTCCGCCGCGCTCCAGCCTCGCTC AGCGGCCCCGGCCTCCCTCTCCGCCGCGCTTCCGCCTCCCGCTCCGCCGCGCTCCAGCCTCGCTC T G FASN Ensembl:ENSG00000169710 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr17:82098051..82098250;chr17:82097926..82098225 26863196 MeRIP-seq:(Medium) rs1568120404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4461524,Human_RBP_ID_9327048,Human_RBP_ID_22532936 Human_Splice_Rec_1884363,Human_Splice_Rec_1884447,Human_Splice_Rec_1884551,Human_Splice_Rec_1884563 Human_miRNA_ID_2716110,Human_miRNA_ID_3052095 RMVar_hsa_circ_117405,RMVar_hsa_circ_187847 101169 RMVar_ID_101169 Human_SNP_ID_634789908 m1A Human chr17 - 82098220 82098220 82098220 GGCGCCGGCCTAGAGGGAGCCAGAGAGACGGCAGCGGCCCCGGCCTCCCTCTCCGCCGCGCTTCA GGCGCCGGCCTAGAGGGAGCCAGAGAGACGGCGGCGGCCCCGGCCTCCCTCTCCGCCGCGCTTCA T C FASN Ensembl:ENSG00000169710 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972533,GSM1972534 HEK293T,ALKBH3 KO;HEPG2 cell line,total RNA Untreated chr17:82098077..82098293;chr17:82098176..82098225 26863410,26863196 MeRIP-seq:(Medium) rs1220581871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465845,Human_RBP_ID_9327048,Human_RBP_ID_22532936 Human_Splice_Rec_1884363,Human_Splice_Rec_1884447,Human_Splice_Rec_1884551,Human_Splice_Rec_1884563 Human_miRNA_ID_2690914,Human_miRNA_ID_2694222 RMVar_hsa_circ_117405,RMVar_hsa_circ_187847 101170 RMVar_ID_101170 Human_SNP_ID_634791122 m1A Human chr17 + 82101597 82101597 82101597 CTCCCTGCCTCCACCCTGCACGCTGTGCCCACACCCCCCCACAACACGTAGGTGAAAGCACAGGC CTCCCTGCCTCCACCCTGCACGCTGTGCCCACCCCCCCCCACAACACGTAGGTGAAAGCACAGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82101559..82101660 32194978 MeRIP-seq:(Medium) rs755270994 Functional Loss SNV dbSNP153 33..33 33 - - - 101171 RMVar_ID_101171 Human_SNP_ID_634791123 m1A Human chr17 + 82101597 82101597 82101597 CTCCCTGCCTCCACCCTGCACGCTGTGCCCACACCCCCCCACAACACGTAGGTGAAAGCACAGGC CTCCCTGCCTCCACCCTGCACGCTGTGCCCACTCCCCCCCACAACACGTAGGTGAAAGCACAGGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82101559..82101660 32194978 MeRIP-seq:(Medium) rs755270994 Functional Loss SNV dbSNP153 33..33 33 - - - 101172 RMVar_ID_101172 Human_SNP_ID_634792667 m1A Human chr17 + 82106318 82106318 82106318 GAAGGCGGGCACACAGGCCTCACTTGGGCGAGAAGAGACCCAGAGACGCATGGCCTTCCTCCTGG GAAGGCGGGCACACAGGCCTCACTTGGGCGAGGAGAGACCCAGAGACGCATGGCCTTCCTCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:82106209..82106328;chr17:82106222..82106349 26863196 MeRIP-seq:(Medium) rs1433636747 Functional Loss SNV dbSNP153 33..33 33 - - - 101173 RMVar_ID_101173 Human_SNP_ID_634794774 m1A Human chr17 + 82114096 82114096 82114096 CCTGGGCCCTGAGGGGGTTCCCTCGTCAGTACACAGAGTGACGCCACAGATGGAAGAGTGGACTG CCTGGGCCCTGAGGGGGTTCCCTCGTCAGTACGCAGAGTGACGCCACAGATGGAAGAGTGGACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82114094..82114340 26863196 MeRIP-seq:(Medium) rs1466421149 Functional Loss SNV dbSNP153 33..33 33 - - - 101174 RMVar_ID_101174 Human_SNP_ID_634806639 m1A Human chr17 + 82154490 82154490 82154490 GTCACACCTCAGTACTTGGGTGGGTGTACACAATACGTGACCTGGTCCGTGGCCCGTGTGCAAAT GTCACACCTCAGTACTTGGGTGGGTGTACACAGTACGTGACCTGGTCCGTGGCCCGTGTGCAAAT A G AC129510.1 Ensembl:ENSG00000265678 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:82154378..82154872;chr17:82154354..82154747 26863196 MeRIP-seq:(Medium) rs1568289708 Functional Loss SNV dbSNP153 33..33 33 - - - 101175 RMVar_ID_101175 Human_SNP_ID_634806954 m1A Human chr17 + 82155493 82155493 82155493 AGCTGCTTCCTGTGCCTTCCGAACCTGCCTCCATGCTAGAGCCCGGGCTCCTGTGAGCAGGGCAG AGCTGCTTCCTGTGCCTTCCGAACCTGCCTCCGTGCTAGAGCCCGGGCTCCTGTGAGCAGGGCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82155454..82155755 32194978 MeRIP-seq:(Medium) rs1487089431 Functional Loss SNV dbSNP153 33..33 33 - - - 101176 RMVar_ID_101176 Human_SNP_ID_634811436 m1A Human chr17 + 82172651 82172651 82172651 GTTTCTCCCACTTACTCACCAGGAGTGGCGGCATCTCCCCCAGCCTCTGGGTCAGGCTGGTTTGC GTTTCTCCCACTTACTCACCAGGAGTGGCGGCCTCTCCCCCAGCCTCTGGGTCAGGCTGGTTTGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82172648..82172849 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 101177 RMVar_ID_101177 Human_SNP_ID_634815825 m1A Human chr17 + 82188320 82188320 82188320 TCGAGGGTCTCGCAGTGGGCCTGCAGCTCCAGAACCCTGGTCTGCAGCTCCTGCAGCTGCTCCAC TCGAGGGTCTCGCAGTGGGCCTGCAGCTCCAGGACCCTGGTCTGCAGCTCCTGCAGCTGCTCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82188271..82193825 26863196 MeRIP-seq:(Medium) rs1163652799 Functional Loss SNV dbSNP153 33..33 33 - - - 101178 RMVar_ID_101178 Human_SNP_ID_634815834 m1A Human chr17 - 82188339 82188339 82188339 GGCGGTGAAGGGAGCCCACGTGGAGCAGCTGCAGGAGCTGCAGACCAGGGTTCTGGAGCTGCAGG GGCGGTGAAGGGAGCCCACGTGGAGCAGCTGCTGGAGCTGCAGACCAGGGTTCTGGAGCTGCAGG T A CCDC57 Ensembl:ENSG00000176155 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82188288..82193924 26863196 MeRIP-seq:(Medium) rs373163923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951506,Human_RBP_ID_9377173,Human_RBP_ID_18989735,Human_RBP_ID_22959314,Human_RBP_ID_26332629,Human_RBP_ID_27814404 Human_Splice_Rec_1884580,Human_Splice_Rec_1884612,Human_Splice_Rec_1884644,Human_Splice_Rec_1884736,Human_Splice_Rec_1884758,Human_Splice_Rec_1884764,Human_Splice_Rec_1884772 RMVar_hsa_circ_6789,RMVar_hsa_circ_31577,RMVar_hsa_circ_25796,RMVar_hsa_circ_333191,RMVar_hsa_circ_265961,RMVar_hsa_circ_356803,RMVar_hsa_circ_333798,RMVar_hsa_circ_187905,RMVar_hsa_circ_337874,RMVar_hsa_circ_369524,RMVar_hsa_circ_12311,RMVar_hsa_circ_187906,RMVar_hsa_circ_187911,RMVar_hsa_circ_88070,RMVar_hsa_circ_266833,RMVar_hsa_circ_376749,RMVar_hsa_circ_98531,RMVar_hsa_circ_26338,RMVar_hsa_circ_187912,RMVar_hsa_circ_284434,RMVar_hsa_circ_336581,RMVar_hsa_circ_359065,RMVar_hsa_circ_335065,RMVar_hsa_circ_269997,RMVar_hsa_circ_24071,RMVar_hsa_circ_187913,RMVar_hsa_circ_187915,RMVar_hsa_circ_187916,RMVar_hsa_circ_187914,RMVar_hsa_circ_25753 101179 RMVar_ID_101179 Human_SNP_ID_634817420 m1A Human chr17 - 82194063 82194063 82194063 GGCAAAGGCTGCAGAGAGTCTGCAGAGGGCAGAGGCCACCAACGCCGAGCTGGAGAGGAAGCTCC GGCAAAGGCTGCAGAGAGTCTGCAGAGGGCAGGGGCCACCAACGCCGAGCTGGAGAGGAAGCTCC T C CCDC57 Ensembl:ENSG00000176155 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82194023..82194124 32194978 MeRIP-seq:(Medium) rs886311829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901242,Human_RBP_ID_3953386,Human_RBP_ID_5526104,Human_RBP_ID_9379381,Human_RBP_ID_18989736,Human_RBP_ID_22959530,Human_RBP_ID_23118993,Human_RBP_ID_27814405 Human_Splice_Rec_1884576,Human_Splice_Rec_1884577,Human_Splice_Rec_1884608,Human_Splice_Rec_1884609,Human_Splice_Rec_1884640,Human_Splice_Rec_1884641,Human_Splice_Rec_1884732,Human_Splice_Rec_1884733,Human_Splice_Rec_1884762,Human_Splice_Rec_1884768,Human_Splice_Rec_1884769 Human_miRNA_ID_2018023 RMVar_hsa_circ_6789,RMVar_hsa_circ_25796,RMVar_hsa_circ_12311,RMVar_hsa_circ_187911,RMVar_hsa_circ_88070,RMVar_hsa_circ_98531,RMVar_hsa_circ_187912,RMVar_hsa_circ_284434,RMVar_hsa_circ_336581,RMVar_hsa_circ_359065,RMVar_hsa_circ_54803,RMVar_hsa_circ_24071,RMVar_hsa_circ_187915,RMVar_hsa_circ_187916,RMVar_hsa_circ_325710,RMVar_hsa_circ_354069,RMVar_hsa_circ_67177,RMVar_hsa_circ_187917 101180 RMVar_ID_101180 Human_SNP_ID_634819651 m1A Human chr17 + 82201733 82201731 82201734 TGGCCTGGGCGAAGGCGGCGTCATAGCGCTCCAGCTCGAGGTCCCGCTCCTCCAGCACCTGAAGG TGGCCTGGGCGAAGGCGGCGTCATAGCGCTC___CTCGAGGTCCCGCTCCTCCAGCACCTGAAGG CCAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82201638..82201889 32194978 MeRIP-seq:(Medium) rs1429184133 Functional Loss DEL dbSNP153 32..34 33 - - - 101181 RMVar_ID_101181 Human_SNP_ID_634821315 m1A Human chr17 - 82207790 82207790 82207790 AAACACCCAAGACATAAACACCCAACAGGTCCACCCCGCCTGCTGCCCAGGCAGAGCCGATTCAC AAACACCCAAGACATAAACACCCAACAGGTCCTCCCCGCCTGCTGCCCAGGCAGAGCCGATTCAC T A CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82207787..82207957 26863196 MeRIP-seq:(Medium) rs886908720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1884725 RMVar_hsa_circ_88070,RMVar_hsa_circ_187912 101182 RMVar_ID_101182 Human_SNP_ID_634822994 m1A Human chr17 - 82213840 82213840 82213840 GGCATCCAGGGAACCAAGTCTAGGCAGAGGCAACTGGCGCAAAGGACCTGAGGCAGAAGAGGGTT GGCATCCAGGGAACCAAGTCTAGGCAGAGGCAGCTGGCGCAAAGGACCTGAGGCAGAAGAGGGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82213792..82213942 26863196 MeRIP-seq:(Medium) rs1226529288 Functional Loss SNV dbSNP153 33..33 33 - - - 101183 RMVar_ID_101183 Human_SNP_ID_634827338 m1A Human chr17 + 82228519 82228519 82228519 AGGAAGAGCCGCCGTCCGCACCGGGACCGGAGAGGAAGCGGAGGTCTGAAGGGGGACAGGTCGGA AGGAAGAGCCGCCGTCCGCACCGGGACCGGAGGGGAAGCGGAGGTCTGAAGGGGGACAGGTCGGA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82228513..82228911 26863196 MeRIP-seq:(Medium) rs1157582729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1884779,Human_Splice_Rec_1884785,Human_Splice_Rec_1884793,Human_Splice_Rec_1884799 RMVar_hsa_circ_86577,RMVar_hsa_circ_187918 101184 RMVar_ID_101184 Human_SNP_ID_634827850 m1A Human chr17 + 82229837 82229837 82229837 AGCCTCCCTGGGTGTTGGGCCAGTCAAGAGACAGGAGCCGCAGAGTGGAAGGGAAGCCCTTAGCT AGCCTCCCTGGGTGTTGGGCCAGTCAAGAGACCGGAGCCGCAGAGTGGAAGGGAAGCCCTTAGCT A C SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82229834..82229993 26863196 MeRIP-seq:(Medium) rs1007128313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190689,Human_RBP_ID_8727332,Human_RBP_ID_18420410,Human_RBP_ID_22416316,Human_RBP_ID_22717214,Human_RBP_ID_22740770 RMVar_hsa_circ_86577,RMVar_hsa_circ_187918 101185 RMVar_ID_101185 Human_SNP_ID_634829831 m1A Human chr17 + 82234616 82234616 82234616 CGGACCTCTGAGGCAGGGACTCCAGGGGGCACAGCACCTGTGGTGGGGACAGGCAGGCAGGCTGG CGGACCTCTGAGGCAGGGACTCCAGGGGGCACGGCACCTGTGGTGGGGACAGGCAGGCAGGCTGG A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82234614..82234721 26863196 MeRIP-seq:(Medium) rs569620200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3544429,Human_RBP_ID_8190721,Human_RBP_ID_8232731,Human_RBP_ID_8727363,Human_RBP_ID_18420435,Human_RBP_ID_21974882,Human_RBP_ID_22717242 RMVar_hsa_circ_86577,RMVar_hsa_circ_187918 101186 RMVar_ID_101186 Human_SNP_ID_634830217 m1A Human chr17 - 82235936 82235936 82235936 AGGCTGACTCAGGCTGCCCGGGTGACCATCCCAGCTGCAGCCTGGCAGGGGAGGGACACGAGCTG AGGCTGACTCAGGCTGCCCGGGTGACCATCCCGGCTGCAGCCTGGCAGGGGAGGGACACGAGCTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82235932..82236150 26863196 MeRIP-seq:(Medium) rs992487036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17903358 101187 RMVar_ID_101187 Human_SNP_ID_634830226 m1A Human chr17 + 82235964 82235964 82235964 CAGCTGGGATGGTCACCCGGGCAGCCTGAGTCAGCCTGCTTTCTCTCTCAGGTGAGGCGGAACCA CAGCTGGGATGGTCACCCGGGCAGCCTGAGTCGGCCTGCTTTCTCTCTCAGGTGAGGCGGAACCA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:82235960..82236261;chr17:82235960..82236250 26863196 MeRIP-seq:(Medium) rs961779859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22544045,Human_RBP_ID_22658100 RMVar_hsa_circ_86577,RMVar_hsa_circ_187918 101188 RMVar_ID_101188 Human_SNP_ID_634830272 m1A Human chr17 + 82236039 82236039 82236039 CCATGGGAGGGGCCGTGGTGGACGAGGGCCCCACAGGCGTCAAGGCCCCTGACGGCGGCTGGGGC CCATGGGAGGGGCCGTGGTGGACGAGGGCCCCGCAGGCGTCAAGGCCCCTGACGGCGGCTGGGGC A G SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82236026..82236050 26863196 MeRIP-seq:(Medium) rs1385640000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765561,Human_RBP_ID_903257,Human_RBP_ID_4464977,Human_RBP_ID_5238006,Human_RBP_ID_18470216,Human_RBP_ID_22444127 Human_Splice_Rec_1884780,Human_Splice_Rec_1884786,Human_Splice_Rec_1884794,Human_Splice_Rec_1884800,Human_Splice_Rec_1884802,Human_Splice_Rec_1884810,Human_Splice_Rec_1884816,Human_Splice_Rec_1884820,Human_Splice_Rec_1884826,Human_Splice_Rec_1884828,Human_Splice_Rec_1884832,Human_Splice_Rec_1884834,Human_Splice_Rec_1884840,Human_Splice_Rec_1884854,Human_Splice_Rec_1884860,Human_Splice_Rec_1884868,Human_Splice_Rec_1884874,Human_Splice_Rec_1884880 RMVar_hsa_circ_86577,RMVar_hsa_circ_187919,RMVar_hsa_circ_187918,RMVar_hsa_circ_312414 101189 RMVar_ID_101189 Human_SNP_ID_634830375 m1A Human chr17 + 82236188 82236188 82236188 ATACAGGAGTTTGGGATCGGCTACAGCGACACAGCCTGGATCTCCTCCATCCTGCTGGCCATGCT ATACAGGAGTTTGGGATCGGCTACAGCGACACGGCCTGGATCTCCTCCATCCTGCTGGCCATGCT A G SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82236176..82236200 26863196 MeRIP-seq:(Medium) rs745808851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765563,Human_RBP_ID_820971,Human_RBP_ID_903257,Human_RBP_ID_4464979,Human_RBP_ID_22444129 Human_Splice_Rec_1884781,Human_Splice_Rec_1884787,Human_Splice_Rec_1884795,Human_Splice_Rec_1884803,Human_Splice_Rec_1884811,Human_Splice_Rec_1884817,Human_Splice_Rec_1884821,Human_Splice_Rec_1884829,Human_Splice_Rec_1884835,Human_Splice_Rec_1884841,Human_Splice_Rec_1884847,Human_Splice_Rec_1884855,Human_Splice_Rec_1884861,Human_Splice_Rec_1884869,Human_Splice_Rec_1884875,Human_Splice_Rec_1884881 Human_miRNA_ID_2370875,Human_miRNA_ID_2707159 RMVar_hsa_circ_86577,RMVar_hsa_circ_187919,RMVar_hsa_circ_187918,RMVar_hsa_circ_312414 101190 RMVar_ID_101190 Human_SNP_ID_634830376 m1A Human chr17 + 82236188 82236188 82236188 ATACAGGAGTTTGGGATCGGCTACAGCGACACAGCCTGGATCTCCTCCATCCTGCTGGCCATGCT ATACAGGAGTTTGGGATCGGCTACAGCGACACTGCCTGGATCTCCTCCATCCTGCTGGCCATGCT A T SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82236176..82236200 26863196 MeRIP-seq:(Medium) rs745808851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765563,Human_RBP_ID_820971,Human_RBP_ID_903257,Human_RBP_ID_4464979,Human_RBP_ID_22444129 Human_Splice_Rec_1884781,Human_Splice_Rec_1884787,Human_Splice_Rec_1884795,Human_Splice_Rec_1884803,Human_Splice_Rec_1884811,Human_Splice_Rec_1884817,Human_Splice_Rec_1884821,Human_Splice_Rec_1884829,Human_Splice_Rec_1884835,Human_Splice_Rec_1884841,Human_Splice_Rec_1884847,Human_Splice_Rec_1884855,Human_Splice_Rec_1884861,Human_Splice_Rec_1884869,Human_Splice_Rec_1884875,Human_Splice_Rec_1884881 Human_miRNA_ID_2370875,Human_miRNA_ID_2707159 RMVar_hsa_circ_86577,RMVar_hsa_circ_187919,RMVar_hsa_circ_187918,RMVar_hsa_circ_312414 101191 RMVar_ID_101191 Human_SNP_ID_634831114 m1A Human chr17 + 82237683 82237683 82237683 CCGTCTACCTCTTCAGCTTCTCCATGTTCTTCAACGGCCTCGCGGACCTGGCGGGTTCTACGGCG CCGTCTACCTCTTCAGCTTCTCCATGTTCTTCCACGGCCTCGCGGACCTGGCGGGTTCTACGGCG A C SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82237125..82237922 26863196 MeRIP-seq:(Medium) rs1455458970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48556,Human_RBP_ID_22444141,Human_RBP_ID_27156999,Human_RBP_ID_27459343 RMVar_hsa_circ_13571,RMVar_hsa_circ_187919,RMVar_hsa_circ_312414 101192 RMVar_ID_101192 Human_SNP_ID_634831129 m1A Human chr17 + 82237710 82237699 82237711 TCTTCAACGGCCTCGCGGACCTGGCGGGTTCTACGGCGGGCGACTACGGCGGCCTCGTGGTCTTC TCTTCAACGGCCTCGCGGACCT____________GGCGGGCGACTACGGCGGCCTCGTGGTCTTC TGGCGGGTTCTAC T SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82237589..82237800 26863196 MeRIP-seq:(Medium) rs754234170 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_765570,Human_RBP_ID_903266,Human_RBP_ID_5238009,Human_RBP_ID_22444141,Human_RBP_ID_27156999,Human_RBP_ID_27459343 RMVar_hsa_circ_13571,RMVar_hsa_circ_187919,RMVar_hsa_circ_312414 101193 RMVar_ID_101193 Human_SNP_ID_634831729 m1A Human chr17 - 82238913 82238913 82238913 TCCCCGTTTTTCTCAGGCTCAGCCTTCAGGAAATGCTCCACCTCCCGCAAGTCCACCCCCGAGTC TCCCCGTTTTTCTCAGGCTCAGCCTTCAGGAAGTGCTCCACCTCCCGCAAGTCCACCCCCGAGTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82238862..82239017 26863196 MeRIP-seq:(Medium) rs372678570 Functional Loss SNV dbSNP153 33..33 33 - - - 101194 RMVar_ID_101194 Human_SNP_ID_634833952 m1A Human chr17 + 82244744 82244744 82244744 AGTAAAGCCATTGGTAACAGAGTAGATCAGCCATGCATTGTCTGCCCTTCACAGCAATAAGGAGA AGTAAAGCCATTGGTAACAGAGTAGATCAGCCGTGCATTGTCTGCCCTTCACAGCAATAAGGAGA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82244708..82244850 26863196 MeRIP-seq:(Medium) rs755470214 Functional Loss SNV dbSNP153 33..33 33 - - - 101195 RMVar_ID_101195 Human_SNP_ID_634833953 m1A Human chr17 - 82244745 82244745 82244745 CTCTCCTTATTGCTGTGAAGGGCAGACAATGCATGGCTGATCTACTCTGTTACCAATGGCTTTAC CTCTCCTTATTGCTGTGAAGGGCAGACAATGCGTGGCTGATCTACTCTGTTACCAATGGCTTTAC T C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82244533..82244850 26863196 MeRIP-seq:(Medium) rs200232591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48565,Human_RBP_ID_1545635,Human_RBP_ID_1871336,Human_RBP_ID_3540106,Human_RBP_ID_4481433,Human_RBP_ID_8466831,Human_RBP_ID_8823902,Human_RBP_ID_9288536,Human_RBP_ID_13203755,Human_RBP_ID_17262488,Human_RBP_ID_17494671,Human_RBP_ID_18297179,Human_RBP_ID_18544421,Human_RBP_ID_18712432,Human_RBP_ID_22443278,Human_RBP_ID_22807565,Human_RBP_ID_23755870,Human_RBP_ID_26646636,Human_RBP_ID_26976049,Human_RBP_ID_27459435 Human_Splice_Rec_1884926,Human_Splice_Rec_1884940,Human_Splice_Rec_1884952,Human_Splice_Rec_1884954,Human_Splice_Rec_1884972,Human_Splice_Rec_1884976,Human_Splice_Rec_1884978,Human_Splice_Rec_1884988,Human_Splice_Rec_1885002,Human_Splice_Rec_1885004 Human_miRNA_ID_979679,Human_miRNA_ID_984410,Human_miRNA_ID_2161417,Human_miRNA_ID_2445919,Human_miRNA_ID_2447308 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_125464,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187924 101196 RMVar_ID_101196 Human_SNP_ID_634834168 m1A Human chr17 - 82245304 82245287 82245304 GGCGTCCACGCTGTGCTCCCTCCTCGGCGGCCACGCGCGCTCGGCGGCTCCTTCCAGCAGGGGCT GGCGTCCACGCTGTGCTCCCTCCTCGGCGGCC_________________CCTTCCAGCAGGGGCT GAGCCGCCGAGCGCGCGT G CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:82245300..82245523;chr17:82245295..82245525 26863196 MeRIP-seq:(Medium) rs752237395 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_8253863,Human_RBP_ID_18487059,Human_RBP_ID_21927799,Human_RBP_ID_21974892,Human_RBP_ID_22475295 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_125464,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187924 101197 RMVar_ID_101197 Human_SNP_ID_634834170 m1A Human chr17 - 82245304 82245288 82245305 GGCGTCCACGCTGTGCTCCCTCCTCGGCGGCCACGCGCGCTCGGCGGCTCCTTCCAGCAGGGGCT GGCGTCCACGCTGTGCTCCCTCCTCGGCGGC_________________TCCTTCCAGCAGGGGCT AGCCGCCGAGCGCGCGTG A CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:82245300..82245523;chr17:82245295..82245525 26863196 MeRIP-seq:(Medium) rs1032043267 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_8253863,Human_RBP_ID_18487059,Human_RBP_ID_21927799,Human_RBP_ID_21974892,Human_RBP_ID_22475295 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_125464,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187924 101198 RMVar_ID_101198 Human_SNP_ID_634834418 m1A Human chr17 - 82245987 82245987 82245987 CCACGGCAAGTAGCTGCTCGTCTCCCATCGGAAGGCAGCACTGGGTGAGTGTGCGCGTGGCGGGC CCACGGCAAGTAGCTGCTCGTCTCCCATCGGACGGCAGCACTGGGTGAGTGTGCGCGTGGCGGGC T G CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82245976..82246050 26863196 MeRIP-seq:(Medium) rs1269344325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236375,Human_RBP_ID_18993106,Human_RBP_ID_21974902,Human_RBP_ID_22807568,Human_RBP_ID_27459438 Human_Splice_Rec_1884939,Human_Splice_Rec_1884950,Human_Splice_Rec_1884951,Human_Splice_Rec_1884953,Human_Splice_Rec_1884970,Human_Splice_Rec_1884971,Human_Splice_Rec_1884974,Human_Splice_Rec_1884975,Human_Splice_Rec_1884986,Human_Splice_Rec_1884987,Human_Splice_Rec_1885000,Human_Splice_Rec_1885001,Human_Splice_Rec_1885018 Human_miRNA_ID_2775684 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_125464,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187924 101199 RMVar_ID_101199 Human_SNP_ID_634835602 m1A Human chr17 - 82249471 82249471 82249471 ACAGCCTCCGGCCGCCTGCGGGGGACGCAGGAAGTGGCTCCCCCCACACCCCTCACCCCTACCTC ACAGCCTCCGGCCGCCTGCGGGGGACGCAGGAGGTGGCTCCCCCCACACCCCTCACCCCTACCTC T C CSNK1D Ensembl:ENSG00000141551 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82249426..82249475 26863196 MeRIP-seq:(Medium) rs550852694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236383,Human_RBP_ID_18191127,Human_RBP_ID_18993109,Human_RBP_ID_22807575 Human_Splice_Rec_1884907,Human_Splice_Rec_1884923,Human_Splice_Rec_1884937,Human_Splice_Rec_1884947,Human_Splice_Rec_1884967,Human_Splice_Rec_1884983,Human_Splice_Rec_1884997,Human_Splice_Rec_1885015,Human_Splice_Rec_1885021 Human_miRNA_ID_3009823 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187925,RMVar_hsa_circ_293756,RMVar_hsa_circ_366424,RMVar_hsa_circ_374594,RMVar_hsa_circ_187926 101200 RMVar_ID_101200 Human_SNP_ID_634835648 m1A Human chr17 - 82249542 82249542 82249542 AGCGGGAGCGCAGGGACCGAGAGGAGCGGCTGAGACACTCGCGGAACCCGGCTACCCGCGGCCTC AGCGGGAGCGCAGGGACCGAGAGGAGCGGCTGGGACACTCGCGGAACCCGGCTACCCGCGGCCTC T C CSNK1D Ensembl:ENSG00000141551 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82249402..82249627 26863196 MeRIP-seq:(Medium) rs207476605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115309,Human_RBP_ID_13203900,Human_RBP_ID_18989740,Human_RBP_ID_22660769,Human_RBP_ID_24559315,Human_RBP_ID_27459441 Human_Splice_Rec_1884906,Human_Splice_Rec_1884922,Human_Splice_Rec_1884936,Human_Splice_Rec_1884946,Human_Splice_Rec_1884966,Human_Splice_Rec_1884982,Human_Splice_Rec_1884996,Human_Splice_Rec_1885014,Human_Splice_Rec_1885020,Human_Splice_Rec_1885028,Human_Splice_Rec_1885040 RMVar_hsa_circ_187922,RMVar_hsa_circ_98693,RMVar_hsa_circ_122752,RMVar_hsa_circ_187923,RMVar_hsa_circ_187925,RMVar_hsa_circ_293756,RMVar_hsa_circ_366424,RMVar_hsa_circ_374594,RMVar_hsa_circ_187926 101201 RMVar_ID_101201 Human_SNP_ID_634837255 m1A Human chr17 + 82253944 82253944 82253944 AGAAGCCAGTGAGCTGAGCCGCCGGAGCCTCGAGAAGCCAGTGAGCTGAGCCGCCGGAGCCTCCA AGAAGCCAGTGAGCTGAGCCGCCGGAGCCTCGTGAAGCCAGTGAGCTGAGCCGCCGGAGCCTCCA A T SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82253939..82254250 26863196 MeRIP-seq:(Medium) rs1257910174 Functional Loss SNV dbSNP153 33..33 33 - - - 101202 RMVar_ID_101202 Human_SNP_ID_634837502 m1A Human chr17 + 82254434 82254434 82254434 AGAAGCCAGTCAGCTGAGCCGCCGGAGCCTCGAGAAGCCAGTCAGCTGAGCCGCCGGAGCCTGGA AGAAGCCAGTCAGCTGAGCCGCCGGAGCCTCGGGAAGCCAGTCAGCTGAGCCGCCGGAGCCTGGA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82254429..82254508 26863196 MeRIP-seq:(Medium) rs1364820829 Functional Loss SNV dbSNP153 33..33 33 - - - 101203 RMVar_ID_101203 Human_SNP_ID_634837759 m1A Human chr17 + 82255004 82255004 82255004 AGCCTCCAGAAGCCAGTCAGCTGAGCCGCCGGAGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGA AGCCTCCAGAAGCCAGTCAGCTGAGCCGCCGGCGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGA A C SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82255002..82255160 26863196 MeRIP-seq:(Medium) rs954007865 Functional Loss SNV dbSNP153 33..33 33 - - - 101204 RMVar_ID_101204 Human_SNP_ID_634837760 m1A Human chr17 + 82255004 82255004 82255004 AGCCTCCAGAAGCCAGTCAGCTGAGCCGCCGGAGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGA AGCCTCCAGAAGCCAGTCAGCTGAGCCGCCGGGGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82255002..82255160 26863196 MeRIP-seq:(Medium) rs954007865 Functional Loss SNV dbSNP153 33..33 33 - - - 101205 RMVar_ID_101205 Human_SNP_ID_634837838 m1A Human chr17 + 82255132 82255132 82255132 AGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGAGCCTCCAGAAGCCAGTGAGCTGGGCCGCCGGA AGCCTCGAGAAGCCAGTGAGCTGAGCCGTCGGGGCCTCCAGAAGCCAGTGAGCTGGGCCGCCGGA A G SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82254735..82255183 26863196 MeRIP-seq:(Medium) rs1179916570 Functional Loss SNV dbSNP153 33..33 33 - - - 101206 RMVar_ID_101206 Human_SNP_ID_634841170 m1A Human chr17 - 82265777 82265777 82265777 TTTCTTTGCCAAGGTACGGACATTGCTGCAGGAGAAGAGGTTGCCATCAAGCTTGAATGTGTCAA TTTCTTTGCCAAGGTACGGACATTGCTGCAGGGGAAGAGGTTGCCATCAAGCTTGAATGTGTCAA T C CSNK1D Ensembl:ENSG00000141551 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82265726..82265862 26863196 MeRIP-seq:(Medium) rs1286892061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50688,Human_RBP_ID_503561,Human_RBP_ID_1545778,Human_RBP_ID_1871395,Human_RBP_ID_3540147,Human_RBP_ID_5498080,Human_RBP_ID_5578066,Human_RBP_ID_6653292,Human_RBP_ID_8466890,Human_RBP_ID_13204525,Human_RBP_ID_18712500,Human_RBP_ID_22544864,Human_RBP_ID_22657165,Human_RBP_ID_22741066,Human_RBP_ID_22958674,Human_RBP_ID_25336559,Human_RBP_ID_26976153,Human_RBP_ID_27670264,Human_RBP_ID_27813246 Human_Splice_Rec_1884896,Human_Splice_Rec_1884897,Human_Splice_Rec_1884912,Human_Splice_Rec_1884913,Human_Splice_Rec_1884928,Human_Splice_Rec_1884929,Human_Splice_Rec_1884956,Human_Splice_Rec_1884957,Human_Splice_Rec_1885006,Human_Splice_Rec_1885007,Human_Splice_Rec_1885030,Human_Splice_Rec_1885031,Human_Splice_Rec_1885058,Human_Splice_Rec_1885059,Human_Splice_Rec_1885066,Human_Splice_Rec_1885067,Human_Splice_Rec_1885072,Human_Splice_Rec_1885073,Human_Splice_Rec_1885076,Human_Splice_Rec_1885077,Human_Splice_Rec_1885082,Human_Splice_Rec_1885083,Human_Splice_Rec_1885090,Human_Splice_Rec_1885091,Human_Splice_Rec_1885094 RMVar_hsa_circ_293756,RMVar_hsa_circ_187926,RMVar_hsa_circ_343316,RMVar_hsa_circ_339301,RMVar_hsa_circ_29402,RMVar_hsa_circ_368813 101207 RMVar_ID_101207 Human_SNP_ID_634841173 m1A Human chr17 + 82265783 82265783 82265783 CATTCAAGCTTGATGGCAACCTCTTCTCCTGCAGCAATGTCCGTACCTTGGCAAAGAAAGAAAAC CATTCAAGCTTGATGGCAACCTCTTCTCCTGCGGCAATGTCCGTACCTTGGCAAAGAAAGAAAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:82265676..82266768 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 101208 RMVar_ID_101208 Human_SNP_ID_634841179 m1A Human chr17 - 82265794 82265794 82265794 TTCCTGTTGTGGTTTTCTTTCTTTGCCAAGGTACGGACATTGCTGCAGGAGAAGAGGTTGCCATC TTCCTGTTGTGGTTTTCTTTCTTTGCCAAGGTGCGGACATTGCTGCAGGAGAAGAGGTTGCCATC T C CSNK1D Ensembl:ENSG00000141551 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82265691..82265846 26863196 MeRIP-seq:(Medium) rs1213286514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50688,Human_RBP_ID_1545778,Human_RBP_ID_1871395,Human_RBP_ID_2526977,Human_RBP_ID_4461791,Human_RBP_ID_5498080,Human_RBP_ID_6653292,Human_RBP_ID_13204525,Human_RBP_ID_22544864,Human_RBP_ID_22657165,Human_RBP_ID_22741066,Human_RBP_ID_22959533,Human_RBP_ID_25332327,Human_RBP_ID_27670264,Human_RBP_ID_27813246 Human_Splice_Rec_1884896,Human_Splice_Rec_1884912,Human_Splice_Rec_1884928,Human_Splice_Rec_1884956,Human_Splice_Rec_1885006,Human_Splice_Rec_1885030,Human_Splice_Rec_1885058,Human_Splice_Rec_1885066,Human_Splice_Rec_1885072,Human_Splice_Rec_1885076,Human_Splice_Rec_1885082,Human_Splice_Rec_1885090,Human_Splice_Rec_1885094 RMVar_hsa_circ_293756,RMVar_hsa_circ_187926,RMVar_hsa_circ_343316,RMVar_hsa_circ_339301,RMVar_hsa_circ_29402,RMVar_hsa_circ_368813 101209 RMVar_ID_101209 Human_SNP_ID_634843271 m1A Human chr17 + 82272575 82272575 82272575 CCAGCATCTTAATCCTGTGTGACTTTCTCTACATTCACCTAAACTTAACCCTTGCTCATTTGCAC CCAGCATCTTAATCCTGTGTGACTTTCTCTACGTTCACCTAAACTTAACCCTTGCTCATTTGCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82272573..82272675 26863196 MeRIP-seq:(Medium) rs1454143802 Functional Loss SNV dbSNP153 33..33 33 - - - 101210 RMVar_ID_101210 Human_SNP_ID_634843637 m1A Human chr17 - 82273398 82273398 82273398 GACCCAGGAAGCGGCCGGGAGGGCAGGAGCGAATCGGGCCGCCGCCGCCATGGAGCTGAGAGTCG GACCCAGGAAGCGGCCGGGAGGGCAGGAGCGAGTCGGGCCGCCGCCGCCATGGAGCTGAGAGTCG T C CSNK1D Ensembl:ENSG00000141551 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82273267..82273700 26863196 MeRIP-seq:(Medium) rs1207926620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50689,Human_RBP_ID_237912,Human_RBP_ID_1066753,Human_RBP_ID_3542170,Human_RBP_ID_4464999,Human_RBP_ID_6653414,Human_RBP_ID_8093138,Human_RBP_ID_9327057,Human_RBP_ID_13204869,Human_RBP_ID_17903409,Human_RBP_ID_18191130,Human_RBP_ID_18419804,Human_RBP_ID_22224726,Human_RBP_ID_22959318 Human_Splice_Rec_1884895,Human_Splice_Rec_1884911,Human_Splice_Rec_1884927,Human_Splice_Rec_1884955,Human_Splice_Rec_1885005,Human_Splice_Rec_1885049,Human_Splice_Rec_1885055,Human_Splice_Rec_1885071,Human_Splice_Rec_1885075,Human_Splice_Rec_1885085,Human_Splice_Rec_1885093 RMVar_hsa_circ_29402 101211 RMVar_ID_101211 Human_SNP_ID_634843696 m1A Human chr17 - 82273519 82273519 82273519 TTGAGGCGCTGGGAGCGGCGGGGCGACAGGAAAGCGATGGTGAAAGCGGGGCCGTGAGGGGGGCG TTGAGGCGCTGGGAGCGGCGGGGCGACAGGAAGGCGATGGTGAAAGCGGGGCCGTGAGGGGGGCG T C CSNK1D Ensembl:ENSG00000141551 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:82272975..82273731;chr17:82273177..82273700;chr17:82273284..82273700 26863196 MeRIP-seq:(Medium) rs1048413780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767097,Human_RBP_ID_3547070,Human_RBP_ID_5238012,Human_RBP_ID_9327058,Human_RBP_ID_18420450,Human_RBP_ID_22716283 101212 RMVar_ID_101212 Human_SNP_ID_634849801 m1A Human chr17 + 82294009 82294009 82294009 CCAGCCTGGGAGACAGAGCGAGACTCCGTCTCAAAATAAATAAATAAAACATATGACTTAGGTAT CCAGCCTGGGAGACAGAGCGAGACTCCGTCTCTAAATAAATAAATAAAACATATGACTTAGGTAT A T AC132872.1 Ensembl:ENSG00000260563 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82293958..82294058 32194978 MeRIP-seq:(Medium) rs1298701466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6616,Human_RBP_ID_3540171,Human_RBP_ID_6657994,Human_RBP_ID_17903416 101213 RMVar_ID_101213 Human_SNP_ID_634851054 m1A Human chr17 - 82298552 82298552 82298552 AGAGCCCGGCCCCGGGCACCTCTACCACCTACAGGGTCCTCAACTGTAGCTCTGACCCTGGAGGA AGAGCCCGGCCCCGGGCACCTCTACCACCTACGGGGTCCTCAACTGTAGCTCTGACCCTGGAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82298524..82298662 26863196 MeRIP-seq:(Medium) rs9898788 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13227,GWAS_ID_13228 101214 RMVar_ID_101214 Human_SNP_ID_634851182 m1A Human chr17 - 82299063 82299063 82299063 ATGACCCCACATTCAACTCCCTGCAGGGCCCGAGGCCACCGTCCAGTGAGGGGCATGCCCTGGGT ATGACCCCACATTCAACTCCCTGCAGGGCCCGCGGCCACCGTCCAGTGAGGGGCATGCCCTGGGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82299061..82299166 26863196 MeRIP-seq:(Medium) rs765814168 Functional Loss SNV dbSNP153 33..33 33 - - - 101215 RMVar_ID_101215 Human_SNP_ID_634858521 m1A Human chr17 - 82321562 82321562 82321562 GAGGCGGCGGCGGCGGCTCGGGCTGGGGGGTCAGGTGGACGCCGCCCTCCGGGGCTGGACGCGCA GAGGCGGCGGCGGCGGCTCGGGCTGGGGGGTCTGGTGGACGCCGCCCTCCGGGGCTGGACGCGCA T A SECTM1 Ensembl:ENSG00000141574 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82321525..82321669 26863196 MeRIP-seq:(Medium) rs866686154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26783046 101216 RMVar_ID_101216 Human_SNP_ID_634858767 m1A Human chr17 - 82322242 82322242 82322242 CCAGACTCCGAGCCCACCCCAAGGCCGCTGGCACTGGTGTTCAAACCCTCACCACTTGGAGCCCT CCAGACTCCGAGCCCACCCCAAGGCCGCTGGCGCTGGTGTTCAAACCCTCACCACTTGGAGCCCT T C SECTM1 Ensembl:ENSG00000141574 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82322193..82322306 26863196 MeRIP-seq:(Medium) rs1275847257 Functional Loss SNV dbSNP153 33..33 33 - - - 101217 RMVar_ID_101217 Human_SNP_ID_634859031 m1A Human chr17 + 82322978 82322978 82322978 AGACAGCAGTGACCACCGCTGGCACAGGCCAGAACCCAGTGTCGGGGGCGGACTGGGGTTCTGCA AGACAGCAGTGACCACCGCTGGCACAGGCCAGTACCCAGTGTCGGGGGCGGACTGGGGTTCTGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82322931..82323048 26863196 MeRIP-seq:(Medium) rs766841465 Functional Loss SNV dbSNP153 33..33 33 - - - 101218 RMVar_ID_101218 Human_SNP_ID_634859534 m1A Human chr17 - 82324552 82324552 82324552 CAGGTGAGGGGAGGCTCGGGGAAGCAAGGGGGAGGGGAGTGAGAGGGGACACGGGGAGGGGAGGG CAGGTGAGGGGAGGCTCGGGGAAGCAAGGGGGGGGGGAGTGAGAGGGGACACGGGGAGGGGAGGG T C SECTM1 Ensembl:ENSG00000141574 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82324548..82324724 26863196 MeRIP-seq:(Medium) rs1274347996 Functional Loss SNV dbSNP153 33..33 33 - - - 101219 RMVar_ID_101219 Human_SNP_ID_634860317 m1A Human chr17 - 82327254 82327254 82327254 TTTCAAGAGCCAGTGACAAGGACCAGGGGCCCAAGTCCCACCAGCCATGCAGACCTGCCCCCTGG TTTCAAGAGCCAGTGACAAGGACCAGGGGCCCGAGTCCCACCAGCCATGCAGACCTGCCCCCTGG T C SECTM1 Ensembl:ENSG00000141574 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82327204..82327295 26863196 MeRIP-seq:(Medium) rs1460726987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1885150,Human_Splice_Rec_1885158,Human_Splice_Rec_1885166,Human_Splice_Rec_1885174,Human_Splice_Rec_1885186,Human_Splice_Rec_1885194,Human_Splice_Rec_1885198 RMVar_hsa_circ_102201,RMVar_hsa_circ_108157,RMVar_hsa_circ_187931,RMVar_hsa_circ_187932 101220 RMVar_ID_101220 Human_SNP_ID_634876671 m1A Human chr17 - 82382710 82382710 82382710 GTCCTCCTCCTCCTCCAAGGCAGGCGCCCGACAGCCCCGTGTGCAGGAGACGCACAGCACTCACC GTCCTCCTCCTCCTCCAAGGCAGGCGCCCGACGGCCCCGTGTGCAGGAGACGCACAGCACTCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82382682..82382787 26863196 MeRIP-seq:(Medium) rs1323279570 Functional Loss SNV dbSNP153 33..33 33 - - - 101221 RMVar_ID_101221 Human_SNP_ID_634878134 m1A Human chr17 - 82386939 82386935 82386940 CCTTCCCCCGTAGCCCCTTGTGAGGCCAGGCCAGGCTCACTGTCCCCACGTGCCCCTCGGCCCTG CCTTCCCCCGTAGCCCCTTGTGAGGCCAGGC_____TCACTGTCCCCACGTGCCCCTCGGCCCTG AGCCTG A lnc-OGFOD3-3,lnc-OGFOD3-3:2 RNACentral:URS00008B7B37,RNACentral:URS00008B3825 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82386895..82386981 26863196 MeRIP-seq:(Medium) rs1461718747 Functional Loss DEL dbSNP153 32..36 33 - - - 101222 RMVar_ID_101222 Human_SNP_ID_634879379 m1A Human chr17 - 82391142 82391142 82391142 TGGAAGCTGGGCTCTCCTGGATGCCCTGACCCAGCTGCCTGGGGAGAGCCCTGGGCCCCTCCTCC TGGAAGCTGGGCTCTCCTGGATGCCCTGACCCGGCTGCCTGGGGAGAGCCCTGGGCCCCTCCTCC T C OGFOD3 Ensembl:ENSG00000181396 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82391093..82391224 26863196 MeRIP-seq:(Medium) rs985749145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_657571,Human_miRNA_ID_692671,Human_miRNA_ID_1302566,Human_miRNA_ID_1357698 101223 RMVar_ID_101223 Human_SNP_ID_634879380 m1A Human chr17 - 82391142 82391142 82391142 TGGAAGCTGGGCTCTCCTGGATGCCCTGACCCAGCTGCCTGGGGAGAGCCCTGGGCCCCTCCTCC TGGAAGCTGGGCTCTCCTGGATGCCCTGACCCCGCTGCCTGGGGAGAGCCCTGGGCCCCTCCTCC T G OGFOD3 Ensembl:ENSG00000181396 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82391093..82391224 26863196 MeRIP-seq:(Medium) rs985749145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_657571,Human_miRNA_ID_692671,Human_miRNA_ID_1302566,Human_miRNA_ID_1357698 101224 RMVar_ID_101224 Human_SNP_ID_634887526 m1A Human chr17 - 82418546 82418546 82418546 CCCTGCGCCGTGCCTGCCTCGCGCTCCCTGTTACGGCGTTCGTCCCCGGGCCTGGCGCCCGCGTC CCCTGCGCCGTGCCTGCCTCGCGCTCCCTGTTGCGGCGTTCGTCCCCGGGCCTGGCGCCCGCGTC T C OGFOD3 Ensembl:ENSG00000181396 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82415364..82419789 26863196 MeRIP-seq:(Medium) rs1199249285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465010,Human_RBP_ID_5498092,Human_RBP_ID_9327061,Human_RBP_ID_18420454,Human_RBP_ID_22444157 101225 RMVar_ID_101225 Human_SNP_ID_634887969 m1A Human chr17 + 82420333 82420333 82420333 GGGAAATTTAGAGCCTGAGACACACGGAGGGAAGGCAGTGTGAAGACCCAGGAGGATGCCCCGCG GGGAAATTTAGAGCCTGAGACACACGGAGGGATGGCAGTGTGAAGACCCAGGAGGATGCCCCGCG A T HEXD Ensembl:ENSG00000169660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82420303..82420512 26863196 MeRIP-seq:(Medium) rs1481223209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715891 RMVar_hsa_circ_96035,RMVar_hsa_circ_90412,RMVar_hsa_circ_187940,RMVar_hsa_circ_187942 101226 RMVar_ID_101226 Human_SNP_ID_634889316 m1A Human chr17 + 82425057 82425057 82425057 AGAAGGCTGGAGGAGGCTGGAGGAGGCCAGAGAAGGCTGGAGAAGGCTGGAGAAGGCTGGAGGAG AGAAGGCTGGAGGAGGCTGGAGGAGGCCAGAGGAGGCTGGAGAAGGCTGGAGAAGGCTGGAGGAG A G HEXD Ensembl:ENSG00000169660 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82425032..82425161 26863196 MeRIP-seq:(Medium) rs1236534345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_98486,RMVar_hsa_circ_356158,RMVar_hsa_circ_376711,RMVar_hsa_circ_187943 101227 RMVar_ID_101227 Human_SNP_ID_634892023 m1A Human chr17 + 82433808 82433808 82433808 TGGAGCTACACCCAGGCGCCCAGCGGCTGCACATCGGGTGTGATGAGGTGGGTACTGTCACCCCA TGGAGCTACACCCAGGCGCCCAGCGGCTGCACCTCGGGTGTGATGAGGTGGGTACTGTCACCCCA A C HEXD Ensembl:ENSG00000169660 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4789773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951511,Human_RBP_ID_18993131 Human_Splice_Rec_1885327,Human_Splice_Rec_1885349,Human_Splice_Rec_1885369,Human_Splice_Rec_1885391,Human_Splice_Rec_1885403,Human_Splice_Rec_1885427,Human_Splice_Rec_1885441,Human_Splice_Rec_1885465,Human_Splice_Rec_1885473,Human_Splice_Rec_1885493 GWAS_ID_13229,GWAS_ID_13230,GWAS_ID_13231,GWAS_ID_13232,GWAS_ID_13233,GWAS_ID_13234,GWAS_ID_13235,GWAS_ID_13236 RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_98486,RMVar_hsa_circ_356158,RMVar_hsa_circ_187943 101228 RMVar_ID_101228 Human_SNP_ID_634892024 m1A Human chr17 + 82433808 82433808 82433808 TGGAGCTACACCCAGGCGCCCAGCGGCTGCACATCGGGTGTGATGAGGTGGGTACTGTCACCCCA TGGAGCTACACCCAGGCGCCCAGCGGCTGCACGTCGGGTGTGATGAGGTGGGTACTGTCACCCCA A G HEXD Ensembl:ENSG00000169660 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4789773 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_3951511,Human_RBP_ID_18993131 Human_Splice_Rec_1885327,Human_Splice_Rec_1885349,Human_Splice_Rec_1885369,Human_Splice_Rec_1885391,Human_Splice_Rec_1885403,Human_Splice_Rec_1885427,Human_Splice_Rec_1885441,Human_Splice_Rec_1885465,Human_Splice_Rec_1885473,Human_Splice_Rec_1885493 GWAS_ID_13229,GWAS_ID_13230,GWAS_ID_13231,GWAS_ID_13232,GWAS_ID_13233,GWAS_ID_13234,GWAS_ID_13235,GWAS_ID_13236 RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_98486,RMVar_hsa_circ_356158,RMVar_hsa_circ_187943 101229 RMVar_ID_101229 Human_SNP_ID_634892584 m1A Human chr17 + 82435771 82435771 82435771 GCAGAACAGCACGGGGAAGTTGTGCCTGTCACACATGCGGGCGGTGGCCAGCGGCGTGAAGGCCC GCAGAACAGCACGGGGAAGTTGTGCCTGTCACCCATGCGGGCGGTGGCCAGCGGCGTGAAGGCCC A C HEXD Ensembl:ENSG00000169660 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82435731..82435814 26863196 MeRIP-seq:(Medium) rs758377023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6653491,Human_RBP_ID_18989757 Human_Splice_Rec_1885328,Human_Splice_Rec_1885350,Human_Splice_Rec_1885370,Human_Splice_Rec_1885392,Human_Splice_Rec_1885404,Human_Splice_Rec_1885428,Human_Splice_Rec_1885442,Human_Splice_Rec_1885466,Human_Splice_Rec_1885474,Human_Splice_Rec_1885494 RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_98486,RMVar_hsa_circ_356158,RMVar_hsa_circ_187943 101230 RMVar_ID_101230 Human_SNP_ID_634894578 m1A Human chr17 + 82441504 82441476 82441505 GGTGAGGGGCAGGTGCAGGTGAGCAGGCAGGCATGGGGCAGGTGCGGCTGAGGGGCAGGTGTGGG GGTGA_____________________________GGGGCAGGTGCGGCTGAGGGGCAGGTGTGGG AGGGGCAGGTGCAGGTGAGCAGGCAGGCAT A HEXD Ensembl:ENSG00000169660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82441380..82441551 26863196 MeRIP-seq:(Medium) rs149360265 Functional Loss DEL dbSNP153 6..34 33 - - - Human_RBP_ID_8190752,Human_RBP_ID_19084793,Human_RBP_ID_21975968 RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_126699,RMVar_hsa_circ_187944 101231 RMVar_ID_101231 Human_SNP_ID_634895480 m1A Human chr17 - 82443961 82443913 82443961 GTGCCTGAGCCCGTGCACCGCCCACAGGACCCATGGCACATTCCCGGTGTGCCTGAGCCCGTGCA GTGCCTGAGCCCGTGCACCGCCCACAGGACCC_________________________________ CGGGTCCTGTGGGCGGTGCACGGGCTCAGGCACACCGGGAATGTGCCAT C CYBC1 Ensembl:ENSG00000178927 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1567905645 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_18712600,Human_RBP_ID_27263277,Human_RBP_ID_27459541 Human_miRNA_ID_1934057,Human_miRNA_ID_2197863,Human_miRNA_ID_2658892,Human_miRNA_ID_2936874 RMVar_hsa_circ_89549,RMVar_hsa_circ_94847,RMVar_hsa_circ_187945,RMVar_hsa_circ_187946 101232 RMVar_ID_101232 Human_SNP_ID_634895499 m1A Human chr17 - 82443961 82443961 82443961 GTGCCTGAGCCCGTGCACCGCCCACAGGACCCATGGCACATTCCCGGTGTGCCTGAGCCCGTGCA GTGCCTGAGCCCGTGCACCGCCCACAGGACCCGTGGCACATTCCCGGTGTGCCTGAGCCCGTGCA T C CYBC1 Ensembl:ENSG00000178927 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11557531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18712600,Human_RBP_ID_27263277,Human_RBP_ID_27459541 Human_miRNA_ID_1934057,Human_miRNA_ID_2197863,Human_miRNA_ID_2658892,Human_miRNA_ID_2936874 RMVar_hsa_circ_89549,RMVar_hsa_circ_94847,RMVar_hsa_circ_187945,RMVar_hsa_circ_187946 101233 RMVar_ID_101233 Human_SNP_ID_634896480 m1A Human chr17 - 82446672 82446672 82446672 ATCTCCAGATAGCCTGGGCTGGAAGCTCTTCTACGTCACAGGCTGCCTGTTTGTGGCTGTGCAGA ATCTCCAGATAGCCTGGGCTGGAAGCTCTTCTGCGTCACAGGCTGCCTGTTTGTGGCTGTGCAGA T C CYBC1 Ensembl:ENSG00000178927 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82446602..82446731 26863196 MeRIP-seq:(Medium) rs1389366087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503629,Human_RBP_ID_898135,Human_RBP_ID_4461996,Human_RBP_ID_5318734,Human_RBP_ID_13205225 Human_Splice_Rec_1885546,Human_Splice_Rec_1885547,Human_Splice_Rec_1885561,Human_Splice_Rec_1885568,Human_Splice_Rec_1885569,Human_Splice_Rec_1885582,Human_Splice_Rec_1885583,Human_Splice_Rec_1885602,Human_Splice_Rec_1885603,Human_Splice_Rec_1885620,Human_Splice_Rec_1885621,Human_Splice_Rec_1885630,Human_Splice_Rec_1885631,Human_Splice_Rec_1885640,Human_Splice_Rec_1885641,Human_Splice_Rec_1885652,Human_Splice_Rec_1885653,Human_Splice_Rec_1885664,Human_Splice_Rec_1885665,Human_Splice_Rec_1885678,Human_Splice_Rec_1885679,Human_Splice_Rec_1885686,Human_Splice_Rec_1885687,Human_Splice_Rec_1885694,Human_Splice_Rec_1885695,Human_Splice_Rec_1885704,Human_Splice_Rec_1885705,Human_Splice_Rec_1885718,Human_Splice_Rec_1885719,Human_Splice_Rec_1885732,Human_Splice_Rec_1885733,Human_Splice_Rec_1885740,Human_Splice_Rec_1885741,Human_Splice_Rec_1885756,Human_Splice_Rec_1885757,Human_Splice_Rec_1885766,Human_Splice_Rec_1885767,Human_Splice_Rec_1885776,Human_Splice_Rec_1885777,Human_Splice_Rec_1885788,Human_Splice_Rec_1885789,Human_Splice_Rec_1885798,Human_Splice_Rec_1885799,Human_Splice_Rec_1885812,Human_Splice_Rec_1885813,Human_Splice_Rec_1885822,Human_Splice_Rec_1885823,Human_Splice_Rec_1885828,Human_Splice_Rec_1885829,Human_Splice_Rec_1885834,Human_Splice_Rec_1885835,Human_Splice_Rec_1885840,Human_Splice_Rec_1885841,Human_Splice_Rec_1885850,Human_Splice_Rec_1885851 RMVar_hsa_circ_36162,RMVar_hsa_circ_3985,RMVar_hsa_circ_94847,RMVar_hsa_circ_187946,RMVar_hsa_circ_353412,RMVar_hsa_circ_114643,RMVar_hsa_circ_187949 101234 RMVar_ID_101234 Human_SNP_ID_634897604 m1A Human chr17 + 82450552 82450550 82450552 CGCCGGGGCCAACCTGCAGCGGAACAGGCGCGAGGCCGCCCGCGACGGGCACGGCGGGACACGGA CGCCGGGGCCAACCTGCAGCGGAACAGGCGC__GGCCGCCCGCGACGGGCACGGCGGGACACGGA CGA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82450504..82450652 26863196 MeRIP-seq:(Medium) rs1293902397 Functional Loss DEL dbSNP153 32..33 33 - - - 101235 RMVar_ID_101235 Human_SNP_ID_634900025 m1A Human chr17 + 82458476 82458475 82458476 GCCGCCGCCGCCGCAGGACCCACGAGAAGCGGAAACCGGCGCAAGGACCCGGTCCCCCCGGCGCC GCCGCCGCCGCCGCAGGACCCACGAGAAGCGG_AACCGGCGCAAGGACCCGGTCCCCCCGGCGCC GA G NARF Ensembl:ENSG00000141562 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82458447..82458573 26863196 MeRIP-seq:(Medium) rs1387554070 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1885873,Human_Splice_Rec_1885877,Human_Splice_Rec_1885895,Human_Splice_Rec_1885897,Human_Splice_Rec_1885899 101236 RMVar_ID_101236 Human_SNP_ID_634900028 m1A Human chr17 + 82458476 82458476 82458476 GCCGCCGCCGCCGCAGGACCCACGAGAAGCGGAAACCGGCGCAAGGACCCGGTCCCCCCGGCGCC GCCGCCGCCGCCGCAGGACCCACGAGAAGCGGCAACCGGCGCAAGGACCCGGTCCCCCCGGCGCC A C NARF Ensembl:ENSG00000141562 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82458447..82458573 26863196 MeRIP-seq:(Medium) rs1303660216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1885873,Human_Splice_Rec_1885877,Human_Splice_Rec_1885895,Human_Splice_Rec_1885897,Human_Splice_Rec_1885899 101237 RMVar_ID_101237 Human_SNP_ID_634900211 m1A Human chr17 + 82458802 82458802 82458802 TGAGGCGCCCGGCCTCCCGCCCGCCGCGCTCCAGATGAAGTGTGAGCACTGCACGCGCAAGGTGA TGAGGCGCCCGGCCTCCCGCCCGCCGCGCTCCGGATGAAGTGTGAGCACTGCACGCGCAAGGTGA A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:82458701..82458872;chr17:82458726..82458909 26863196 MeRIP-seq:(Medium) rs770671206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503640,Human_RBP_ID_4462060,Human_RBP_ID_9327070,Human_RBP_ID_18419809,Human_RBP_ID_26758609 Human_Splice_Rec_1885907,Human_Splice_Rec_1885923,Human_Splice_Rec_1885935,Human_Splice_Rec_1885953,Human_Splice_Rec_1885973,Human_Splice_Rec_1885977,Human_Splice_Rec_1885997,Human_Splice_Rec_1886003,Human_Splice_Rec_1886015,Human_Splice_Rec_1886031,Human_Splice_Rec_1886041,Human_Splice_Rec_1886053,Human_Splice_Rec_1886073,Human_Splice_Rec_1886091,Human_Splice_Rec_1886097 Human_miRNA_ID_1000996 101238 RMVar_ID_101238 Human_SNP_ID_634900214 m1A Human chr17 - 82458805 82458805 82458805 CGCTCACCTTGCGCGTGCAGTGCTCACACTTCATCTGGAGCGCGGCGGGCGGGAGGCCGGGCGCC CGCTCACCTTGCGCGTGCAGTGCTCACACTTCCTCTGGAGCGCGGCGGGCGGGAGGCCGGGCGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82458754..82458881 26863196 MeRIP-seq:(Medium) rs1474981666 Functional Loss SNV dbSNP153 33..33 33 - - - 101239 RMVar_ID_101239 Human_SNP_ID_634901283 m1A Human chr17 + 82462187 82462186 82462188 AGTGGGCGCCCTGCCAGGTCAGTGATGGACACAGGGTGAGAGGAGTTGGGTTGGGGTTAATGGAG AGTGGGCGCCCTGCCAGGTCAGTGATGGACAC__GGTGAGAGGAGTTGGGTTGGGGTTAATGGAG CAG C NARF Ensembl:ENSG00000141562 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82462185..82462969 26863196 MeRIP-seq:(Medium) rs909419398 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1091363,Human_RBP_ID_24371549 RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952 101240 RMVar_ID_101240 Human_SNP_ID_634901284 m1A Human chr17 + 82462187 82462187 82462187 AGTGGGCGCCCTGCCAGGTCAGTGATGGACACAGGGTGAGAGGAGTTGGGTTGGGGTTAATGGAG AGTGGGCGCCCTGCCAGGTCAGTGATGGACACGGGGTGAGAGGAGTTGGGTTGGGGTTAATGGAG A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82462185..82462969 26863196 MeRIP-seq:(Medium) rs1281971741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1091363,Human_RBP_ID_24371549 RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952 101241 RMVar_ID_101241 Human_SNP_ID_634901711 m1A Human chr17 + 82463823 82463823 82463823 GAGTGCAAACCCAGAGCCAGCACTGAGTTGTAAAGTTCTGAGCCTCAAGGGAGAGGCCAGGGCTG GAGTGCAAACCCAGAGCCAGCACTGAGTTGTACAGTTCTGAGCCTCAAGGGAGAGGCCAGGGCTG A C NARF,AC132938.6 Ensembl:ENSG00000141562,Ensembl:ENSG00000279744 Protein coding,Other intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:82463821..82463950;chr17:82463816..82463914 26863196,32194978 MeRIP-seq:(Medium) rs911680316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9077147 RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952 101242 RMVar_ID_101242 Human_SNP_ID_634904435 m1A Human chr17 - 82472672 82472672 82472672 GCTCACCAGGACAGGCAGAGGTCAGCATGGGCAGGGTGCGTTCCTCCTCACTGTGCTGGCGATAG GCTCACCAGGACAGGCAGAGGTCAGCATGGGCCGGGTGCGTTCCTCCTCACTGTGCTGGCGATAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82472624..82472734 26863196 MeRIP-seq:(Medium) rs1253076243 Functional Loss SNV dbSNP153 33..33 33 - - - 101243 RMVar_ID_101243 Human_SNP_ID_634909038 m1A Human chr17 + 82488075 82488075 82488075 GGAGCTGTACCAGGAGTGGCTGGAGGGGATCAACTCCCCCAAGGCCCGAGAGGTGCTGCATACCA GGAGCTGTACCAGGAGTGGCTGGAGGGGATCAGCTCCCCCAAGGCCCGAGAGGTGCTGCATACCA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs370872366 Functional Loss SNV dbSNP153 33..33 33 - - - 101244 RMVar_ID_101244 Human_SNP_ID_634910979 m1A Human chr17 + 82494711 82494711 82494711 ATGGGCCACAGGCTGCCCAGTCAGGAAAGAAAAGGGAGTCTATAGCAGAGGATGGTTTCGATCCA ATGGGCCACAGGCTGCCCAGTCAGGAAAGAAAGGGGAGTCTATAGCAGAGGATGGTTTCGATCCA A G lnc-NARF-2,lnc-NARF-2:2 RNACentral:URS0000D59A89,RNACentral:URS0000D574BC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82494608..82494721 26863196 MeRIP-seq:(Medium) rs563671222 Functional Loss SNV dbSNP153 33..33 33 - - - 101245 RMVar_ID_101245 Human_SNP_ID_634911013 m1A Human chr17 - 82494736 82494736 82494736 GCTGGGCCCATAACCCAGAGGTCGATGGATCGAAACCATCCTCTGCTATAGACTCCCTTTTCTTT GCTGGGCCCATAACCCAGAGGTCGATGGATCGGAACCATCCTCTGCTATAGACTCCCTTTTCTTT T C tRNA-iMet-CAT-1-1,TRX-CAT1-1 RNACentral:URS000030BAD5,RNACentral:URS0000326EAC tRNA,tRNA exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs925614841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1545922,Human_RBP_ID_1871476,Human_RBP_ID_5248371,Human_RBP_ID_17586833,Human_RBP_ID_18712638,Human_RBP_ID_20284035,Human_RBP_ID_22808002,Human_RBP_ID_23129949,Human_RBP_ID_25332542,Human_RBP_ID_26977375 101246 RMVar_ID_101246 Human_SNP_ID_634919014 m1A Human chr17 - 82519794 82519794 82519794 GGCCGCGCGGGTCGTCGGCCGCCGCGCACCGGAGCTGAGGGAGGGGGCCGAGCGGAGGCCGCCGG GGCCGCGCGGGTCGTCGGCCGCCGCGCACCGGGGCTGAGGGAGGGGGCCGAGCGGAGGCCGCCGG T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82519743..82519875 26863196 MeRIP-seq:(Medium) rs1474907682 Functional Loss SNV dbSNP153 33..33 33 - - - 101247 RMVar_ID_101247 Human_SNP_ID_634919015 m1A Human chr17 - 82519794 82519794 82519794 GGCCGCGCGGGTCGTCGGCCGCCGCGCACCGGAGCTGAGGGAGGGGGCCGAGCGGAGGCCGCCGG GGCCGCGCGGGTCGTCGGCCGCCGCGCACCGGCGCTGAGGGAGGGGGCCGAGCGGAGGCCGCCGG T G RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82519743..82519875 26863196 MeRIP-seq:(Medium) rs1474907682 Functional Loss SNV dbSNP153 33..33 33 - - - 101248 RMVar_ID_101248 Human_SNP_ID_634921162 m1A Human chr17 + 82526332 82526332 82526332 AGGAGATGGCCAAGGGACATGGCTTGGCAATCAGGAAGTCTTGGGCAGCCTTTGAGAGGGCTGTT AGGAGATGGCCAAGGGACATGGCTTGGCAATCGGGAAGTCTTGGGCAGCCTTTGAGAGGGCTGTT A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82526329..82526445 26863196 MeRIP-seq:(Medium) rs1251500150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13205833,Human_RBP_ID_17129398 RMVar_hsa_circ_187962,RMVar_hsa_circ_86420,RMVar_hsa_circ_92070,RMVar_hsa_circ_267415,RMVar_hsa_circ_80870,RMVar_hsa_circ_84775,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_187963,RMVar_hsa_circ_187960,RMVar_hsa_circ_187961 101249 RMVar_ID_101249 Human_SNP_ID_634931616 m1A Human chr17 + 82563382 82563382 82563382 CCAGGTGCACATTCAGGTTCCCGAGCACAAACATCAAGATAACGTTCACTGCCCTGTCCAGCGAG CCAGGTGCACATTCAGGTTCCCGAGCACAAACGTCAAGATAACGTTCACTGCCCTGTCCAGCGAG A G FOXK2 Ensembl:ENSG00000141568 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82563366..82571744 32194978 MeRIP-seq:(Medium) rs760266857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904146,Human_RBP_ID_1011269,Human_RBP_ID_1545943,Human_RBP_ID_3540300,Human_RBP_ID_8467044,Human_RBP_ID_17262505,Human_RBP_ID_17378597,Human_RBP_ID_18712671 Human_Splice_Rec_1886142,Human_Splice_Rec_1886160,Human_Splice_Rec_1886176,Human_Splice_Rec_1886180,Human_Splice_Rec_1886186,Human_Splice_Rec_1886194 Human_miRNA_ID_2458256,Human_miRNA_ID_2458257,Human_miRNA_ID_2458258,Human_miRNA_ID_2463179,Human_miRNA_ID_2463180,Human_miRNA_ID_2463181 RMVar_hsa_circ_187962,RMVar_hsa_circ_86420,RMVar_hsa_circ_92070,RMVar_hsa_circ_267415,RMVar_hsa_circ_80870,RMVar_hsa_circ_84775,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_187963,RMVar_hsa_circ_187967,RMVar_hsa_circ_281876,RMVar_hsa_circ_187960,RMVar_hsa_circ_187961,RMVar_hsa_circ_293598,RMVar_hsa_circ_311160,RMVar_hsa_circ_359641,RMVar_hsa_circ_304633,RMVar_hsa_circ_285292,RMVar_hsa_circ_187969,RMVar_hsa_circ_273153,RMVar_hsa_circ_187968,RMVar_hsa_circ_187965,RMVar_hsa_circ_187966 101250 RMVar_ID_101250 Human_SNP_ID_634934072 m1A Human chr17 - 82571748 82571748 82571748 CATCGTAATCGCCTGAACTATCAGCTGCGCGTAGGAGTAAGGCGGCTTTGAATCATCCTGTATTT CATCGTAATCGCCTGAACTATCAGCTGCGCGTGGGAGTAAGGCGGCTTTGAATCATCCTGTATTT T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82571743..82571944 32194978 MeRIP-seq:(Medium) rs1344478381 Functional Loss SNV dbSNP153 33..33 33 - - - 101251 RMVar_ID_101251 Human_SNP_ID_634937717 m1A Human chr17 + 82584187 82584187 82584187 ATCCAGGAAGCCCGGTTTGCCCAGAGCGCCCCAGGTGAGACAGCGGGAGAGGAAGCGAGGGCCCC ATCCAGGAAGCCCGGTTTGCCCAGAGCGCCCCGGGTGAGACAGCGGGAGAGGAAGCGAGGGCCCC A G FOXK2 Ensembl:ENSG00000141568 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82584138..82585984 32194978 MeRIP-seq:(Medium) rs1180214440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904157,Human_RBP_ID_18470316 Human_Splice_Rec_1886151,Human_Splice_Rec_1886169,Human_Splice_Rec_1886205 RMVar_hsa_circ_2831,RMVar_hsa_circ_86420,RMVar_hsa_circ_267415,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_187963,RMVar_hsa_circ_281876,RMVar_hsa_circ_311160,RMVar_hsa_circ_359641,RMVar_hsa_circ_187965,RMVar_hsa_circ_187966,RMVar_hsa_circ_108301,RMVar_hsa_circ_20959,RMVar_hsa_circ_121923,RMVar_hsa_circ_187971,RMVar_hsa_circ_274499,RMVar_hsa_circ_301071,RMVar_hsa_circ_187972,RMVar_hsa_circ_187973,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_347737,RMVar_hsa_circ_187975 101252 RMVar_ID_101252 Human_SNP_ID_634938598 m1A Human chr17 - 82586243 82586196 82586244 CTCTCCTCCTTTCCCCCCCCGGCCCACCTTTCACCTCCCTGTGGTCTCCCCTCTCCTCCTTTCCC CTCTCCTCCTTTCCCCCCCCGGCCCACCTTT__________________________________ CAAAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTG C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82586191..82586289 26863196 MeRIP-seq:(Medium) rs748319351 Functional Loss DEL dbSNP153 32..65 33 - - - 101253 RMVar_ID_101253 Human_SNP_ID_634938600 m1A Human chr17 + 82586198 82586198 82586198 GGCCCAGGAGAATGGAGACCACAGGGAAGTCAAAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAG GGCCCAGGAGAATGGAGACCACAGGGAAGTCAGAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAG A G FOXK2 Ensembl:ENSG00000141568 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82586183..82587146 32194978 MeRIP-seq:(Medium) rs771880437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190757 Human_Splice_Rec_1886153,Human_Splice_Rec_1886171,Human_Splice_Rec_1886209 RMVar_hsa_circ_2831,RMVar_hsa_circ_267415,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_281876,RMVar_hsa_circ_311160,RMVar_hsa_circ_187965,RMVar_hsa_circ_187966,RMVar_hsa_circ_108301,RMVar_hsa_circ_20959,RMVar_hsa_circ_121923,RMVar_hsa_circ_187971,RMVar_hsa_circ_301071,RMVar_hsa_circ_187973,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_187975,RMVar_hsa_circ_47221,RMVar_hsa_circ_123202,RMVar_hsa_circ_187976 101254 RMVar_ID_101254 Human_SNP_ID_634938601 m1A Human chr17 + 82586198 82586198 82586198 GGCCCAGGAGAATGGAGACCACAGGGAAGTCAAAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAG GGCCCAGGAGAATGGAGACCACAGGGAAGTCATAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAG A T FOXK2 Ensembl:ENSG00000141568 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82586183..82587146 32194978 MeRIP-seq:(Medium) rs771880437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8190757 Human_Splice_Rec_1886153,Human_Splice_Rec_1886171,Human_Splice_Rec_1886209 RMVar_hsa_circ_2831,RMVar_hsa_circ_267415,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_281876,RMVar_hsa_circ_311160,RMVar_hsa_circ_187965,RMVar_hsa_circ_187966,RMVar_hsa_circ_108301,RMVar_hsa_circ_20959,RMVar_hsa_circ_121923,RMVar_hsa_circ_187971,RMVar_hsa_circ_301071,RMVar_hsa_circ_187973,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_187975,RMVar_hsa_circ_47221,RMVar_hsa_circ_123202,RMVar_hsa_circ_187976 101255 RMVar_ID_101255 Human_SNP_ID_634938605 m1A Human chr17 + 82586214 82586202 82586215 GACCACAGGGAAGTCAAAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTGAA GACCACAGGGAAGTCAAAGGT_____________AGGAGGAGAGGGGAGACCACAGGGAGGTGAA TAGGCGGAGGGGAA T FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82586206..82586272 26863196 MeRIP-seq:(Medium) rs770943555 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_262470,Human_RBP_ID_8190757,Human_RBP_ID_9423751,Human_RBP_ID_22523851 RMVar_hsa_circ_2831,RMVar_hsa_circ_267415,RMVar_hsa_circ_281876,RMVar_hsa_circ_187965,RMVar_hsa_circ_20959,RMVar_hsa_circ_301071,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_187975,RMVar_hsa_circ_123202,RMVar_hsa_circ_187976 101256 RMVar_ID_101256 Human_SNP_ID_634938650 m1A Human chr17 + 82586214 82586214 82586214 GACCACAGGGAAGTCAAAGGTAGGCGGAGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTGAA GACCACAGGGAAGTCAAAGGTAGGCGGAGGGGGAAGGAGGAGAGGGGAGACCACAGGGAGGTGAA A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82586206..82586272 26863196 MeRIP-seq:(Medium) rs1168895447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262470,Human_RBP_ID_8190757,Human_RBP_ID_9423751,Human_RBP_ID_22523851 RMVar_hsa_circ_2831,RMVar_hsa_circ_267415,RMVar_hsa_circ_281876,RMVar_hsa_circ_187965,RMVar_hsa_circ_20959,RMVar_hsa_circ_301071,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_187975,RMVar_hsa_circ_123202,RMVar_hsa_circ_187976 101257 RMVar_ID_101257 Human_SNP_ID_634938692 m1A Human chr17 + 82586234 82586234 82586234 TAGGCGGAGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTGAAAGGTGGGCCGGGGGGGGAAA TAGGCGGAGGGGAAAGGAGGAGAGGGGAGACCTCAGGGAGGTGAAAGGTGGGCCGGGGGGGGAAA A T FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82586188..82586282 26863196 MeRIP-seq:(Medium) rs781727931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6626,Human_RBP_ID_262470,Human_RBP_ID_3542184,Human_RBP_ID_5237809,Human_RBP_ID_8190757,Human_RBP_ID_8232108,Human_RBP_ID_8941869,Human_RBP_ID_9327076,Human_RBP_ID_9423202,Human_RBP_ID_22523851,Human_RBP_ID_26783062 RMVar_hsa_circ_2831,RMVar_hsa_circ_267415,RMVar_hsa_circ_281876,RMVar_hsa_circ_187965,RMVar_hsa_circ_20959,RMVar_hsa_circ_301071,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_187975,RMVar_hsa_circ_123202,RMVar_hsa_circ_187976 101258 RMVar_ID_101258 Human_SNP_ID_634938700 m1A Human chr17 - 82586243 82586240 82586244 CTCTCCTCCTTTCCCCCCCCGGCCCACCTTTCACCTCCCTGTGGTCTCCCCTCTCCTCCTTTCCC CTCTCCTCCTTTCCCCCCCCGGCCCACCTTT____TCCCTGTGGTCTCCCCTCTCCTCCTTTCCC AGGTG A RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82586191..82586289 26863196 MeRIP-seq:(Medium) rs778934020 Functional Loss DEL dbSNP153 32..35 33 - - - 101259 RMVar_ID_101259 Human_SNP_ID_634938712 m1A Human chr17 - 82586342 82586244 82586343 CCCTCTCCTCCTTTCCCCTCCGCCTACCTTTGACCTCCCTGTGGTCTCCCCTCTCCTCCTTTCCC CCCTCTCCTCCTTTCCCCTCCGCCTACCTTT__________________________________ GAAAGGTGGGCCGGGGGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTCAAAGGTGGGCCGGGGGGGAAAGGAGGAGAGGGGAGACCACAGGGAGGTC G RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82586276..82586404 26863196 MeRIP-seq:(Medium) rs1567984912 Functional Loss DEL dbSNP153 32..65 33 - - - 101260 RMVar_ID_101260 Human_SNP_ID_634940120 m1A Human chr17 + 82588373 82588373 82588373 TAAACCTGGTGGCACTGCAGGTAGCTGGGAGGAGATGGAAGCCGGGAGGGCTGGCGATTGGAGGG TAAACCTGGTGGCACTGCAGGTAGCTGGGAGGGGATGGAAGCCGGGAGGGCTGGCGATTGGAGGG A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82588367..82588483 26863196 MeRIP-seq:(Medium) rs1162434917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5318738,Human_RBP_ID_6653780,Human_RBP_ID_8190761,Human_RBP_ID_13207730,Human_RBP_ID_17068072,Human_RBP_ID_23756381,Human_RBP_ID_26783064 101261 RMVar_ID_101261 Human_SNP_ID_634941525 m1A Human chr17 + 82593406 82593400 82593407 AGGGAAAGAGGAAGGAAGGAAAGGAGAGCGATAGGCACAGAGGAAGGTAGATGAAGCCCCGCGCC AGGGAAAGAGGAAGGAAGGAAAGGAGA_______GCACAGAGGAAGGTAGATGAAGCCCCGCGCC AGCGATAG A FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82593400..82593533 26863196 MeRIP-seq:(Medium) rs1371739053 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_50693,Human_RBP_ID_3547845,Human_RBP_ID_5185805,Human_RBP_ID_8232524,Human_RBP_ID_8727758,Human_RBP_ID_13207935,Human_RBP_ID_17207158,Human_RBP_ID_18487943 101262 RMVar_ID_101262 Human_SNP_ID_634941528 m1A Human chr17 + 82593406 82593406 82593406 AGGGAAAGAGGAAGGAAGGAAAGGAGAGCGATAGGCACAGAGGAAGGTAGATGAAGCCCCGCGCC AGGGAAAGAGGAAGGAAGGAAAGGAGAGCGATGGGCACAGAGGAAGGTAGATGAAGCCCCGCGCC A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82593400..82593533 26863196 MeRIP-seq:(Medium) rs1437623507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50693,Human_RBP_ID_3547845,Human_RBP_ID_5185805,Human_RBP_ID_8232524,Human_RBP_ID_8727758,Human_RBP_ID_13207935,Human_RBP_ID_17207158,Human_RBP_ID_18487943 101263 RMVar_ID_101263 Human_SNP_ID_634941529 m1A Human chr17 + 82593410 82593408 82593410 AAAGAGGAAGGAAGGAAAGGAGAGCGATAGGCACAGAGGAAGGTAGATGAAGCCCCGCGCCCCCC AAAGAGGAAGGAAGGAAAGGAGAGCGATAGG__CAGAGGAAGGTAGATGAAGCCCCGCGCCCCCC GCA G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82593405..82593542 26863196 MeRIP-seq:(Medium) rs1280813807 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_50693,Human_RBP_ID_3547845,Human_RBP_ID_5185805,Human_RBP_ID_8232524,Human_RBP_ID_8727758,Human_RBP_ID_13207935,Human_RBP_ID_17207158,Human_RBP_ID_18487943 101264 RMVar_ID_101264 Human_SNP_ID_634941532 m1A Human chr17 + 82593410 82593410 82593410 AAAGAGGAAGGAAGGAAAGGAGAGCGATAGGCACAGAGGAAGGTAGATGAAGCCCCGCGCCCCCC AAAGAGGAAGGAAGGAAAGGAGAGCGATAGGCTCAGAGGAAGGTAGATGAAGCCCCGCGCCCCCC A T FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82593405..82593542 26863196 MeRIP-seq:(Medium) rs1389697102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50693,Human_RBP_ID_3547845,Human_RBP_ID_5185805,Human_RBP_ID_8232524,Human_RBP_ID_8727758,Human_RBP_ID_13207935,Human_RBP_ID_17207158,Human_RBP_ID_18487943 101265 RMVar_ID_101265 Human_SNP_ID_634944050 m1A Human chr17 + 82601375 82601375 82601375 CGCATCGGCCTCCCTGCCCACAAAGCGCCACAACGGTGACCAGCCGGAGCAGCCGGAGCTGAAGC CGCATCGGCCTCCCTGCCCACAAAGCGCCACATCGGTGACCAGCCGGAGCAGCCGGAGCTGAAGC A T FOXK2 Ensembl:ENSG00000141568 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82601326..82601548 26863196 MeRIP-seq:(Medium) rs1050277971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13208282 Human_Splice_Rec_1886158,Human_Splice_Rec_1886174,Human_Splice_Rec_1886212,Human_Splice_Rec_1886218 101266 RMVar_ID_101266 Human_SNP_ID_634944060 m1A Human chr17 + 82601384 82601384 82601384 CTCCCTGCCCACAAAGCGCCACAACGGTGACCAGCCGGAGCAGCCGGAGCTGAAGCGGATCAAGA CTCCCTGCCCACAAAGCGCCACAACGGTGACCGGCCGGAGCAGCCGGAGCTGAAGCGGATCAAGA A G FOXK2 Ensembl:ENSG00000141568 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:82601301..82601483;chr17:82601255..82601435 26863196 MeRIP-seq:(Medium) rs763245322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13208282 Human_Splice_Rec_1886158,Human_Splice_Rec_1886174,Human_Splice_Rec_1886212,Human_Splice_Rec_1886218 101267 RMVar_ID_101267 Human_SNP_ID_634948801 m1A Human chr17 - 82615147 82615147 82615147 ACGGGGGGTCTCCTGGTTACATTTTGGATTAAACCTGTTTCCCGGTTATGTGTAGGGAACAGCAG ACGGGGGGTCTCCTGGTTACATTTTGGATTAATCCTGTTTCCCGGTTATGTGTAGGGAACAGCAG T A WDR45B Ensembl:ENSG00000141580 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82614960..82615200 32194978 MeRIP-seq:(Medium) rs1418743388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503802,Human_RBP_ID_1546141,Human_RBP_ID_1871624,Human_RBP_ID_6653961,Human_RBP_ID_8467204,Human_RBP_ID_9077192,Human_RBP_ID_13208571,Human_RBP_ID_17903565,Human_RBP_ID_23756454,Human_RBP_ID_26458554 Human_miRNA_ID_736243,Human_miRNA_ID_1738379 RMVar_hsa_circ_97117,RMVar_hsa_circ_114070,RMVar_hsa_circ_108332,RMVar_hsa_circ_187978,RMVar_hsa_circ_187980,RMVar_hsa_circ_90466,RMVar_hsa_circ_187979,RMVar_hsa_circ_187977 101268 RMVar_ID_101268 Human_SNP_ID_634952625 m1A Human chr17 - 82627677 82627677 82627677 GGACCGGGCTGTGCGCACTGAGAGAGGAACGGACGGGGAGGGAGCAATGGTTGGCAGAGAGAGAT GGACCGGGCTGTGCGCACTGAGAGAGGAACGGGCGGGGAGGGAGCAATGGTTGGCAGAGAGAGAT T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82627476..82627848 26863196 MeRIP-seq:(Medium) rs781708944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6654022,Human_RBP_ID_13208833 RMVar_hsa_circ_97117,RMVar_hsa_circ_187980,RMVar_hsa_circ_90466,RMVar_hsa_circ_187979,RMVar_hsa_circ_187981,RMVar_hsa_circ_97645,RMVar_hsa_circ_187983,RMVar_hsa_circ_106397,RMVar_hsa_circ_331308,RMVar_hsa_circ_187985,RMVar_hsa_circ_187984,RMVar_hsa_circ_326693,RMVar_hsa_circ_2548 101269 RMVar_ID_101269 Human_SNP_ID_634955292 m1A Human chr17 - 82636701 82636701 82636701 AGAAAGTCGAGTTCGAGAACAAAGGATAAGGAAGTTAACAGGCTAAATAAACCCTTTGAAGAGAA AGAAAGTCGAGTTCGAGAACAAAGGATAAGGACGTTAACAGGCTAAATAAACCCTTTGAAGAGAA T G WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82636693..82636831 26863196 MeRIP-seq:(Medium) rs140206678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13209148 RMVar_hsa_circ_97117,RMVar_hsa_circ_187980,RMVar_hsa_circ_90466,RMVar_hsa_circ_187979,RMVar_hsa_circ_187981,RMVar_hsa_circ_97645,RMVar_hsa_circ_187983,RMVar_hsa_circ_106397 101270 RMVar_ID_101270 Human_SNP_ID_634959153 m1A Human chr17 - 82648385 82648385 82648385 GGCCCGAAGGGACCAGGCCGCCGTCCCCAGCGAGAGGCATGCAGCGCTGAGGAGCGGCGACCCAG GGCCCGAAGGGACCAGGCCGCCGTCCCCAGCGGGAGGCATGCAGCGCTGAGGAGCGGCGACCCAG T C WDR45B Ensembl:ENSG00000141580 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82648293..82648387 26863196 MeRIP-seq:(Medium) rs1383348171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465020,Human_RBP_ID_22589071 RMVar_hsa_circ_187980,RMVar_hsa_circ_90466 101271 RMVar_ID_101271 Human_SNP_ID_634966652 m1A Human chr17 + 82671246 82671246 82671246 TCACACGCTCCCTGTACTCACTGACACACCCCAACCCTGTAACCCTAACACACACAGTCACACAT TCACACGCTCCCTGTACTCACTGACACACCCCCACCCTGTAACCCTAACACACACAGTCACACAT A C lnc-FOXK2-2,lnc-FOXK2-2:2 RNACentral:URS00008B8A41,RNACentral:URS00008B55C2 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:82671129..82671462;chr17:82671211..82671340 26863196 MeRIP-seq:(Medium) rs1405611225 Functional Loss SNV dbSNP153 33..33 33 - - - 101272 RMVar_ID_101272 Human_SNP_ID_634966780 m1A Human chr17 - 82671538 82671426 82671538 TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTGAGTGTGTGTGTTAGAGTTACAGGGGTGGGGTGT TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTG_________________________________ ACACACGCTCCCTGTACTAACTGACACACCCCACCCCTGTAACTCTAACACACACTCACATGCTCCCTGTACTCACTGACACACCCCACCCCTGTAACTCTAACACACACACT A RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82671528..82671599 26863196 MeRIP-seq:(Medium) rs1568036516 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_23756676 101273 RMVar_ID_101273 Human_SNP_ID_634966851 m1A Human chr17 - 82671538 82671534 82671538 TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTGAGTGTGTGTGTTAGAGTTACAGGGGTGGGGTGT TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTG____TGTGTGTTAGAGTTACAGGGGTGGGGTGT ACACT A RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82671528..82671599 26863196 MeRIP-seq:(Medium) rs1317249039 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23756676 101274 RMVar_ID_101274 Human_SNP_ID_634966853 m1A Human chr17 - 82671538 82671536 82671538 TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTGAGTGTGTGTGTTAGAGTTACAGGGGTGGGGTGT TGGGGTGTGTCAGTGAGTACAGGGAGCGTGTG__TGTGTGTGTTAGAGTTACAGGGGTGGGGTGT ACT A RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82671528..82671599 26863196 MeRIP-seq:(Medium) rs1568036630 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23756676 101275 RMVar_ID_101275 Human_SNP_ID_634967098 m1A Human chr17 - 82672155 82672155 82672155 GCATGTGAGTGTGTGTTAGAGTTACAGGGGTGAGCTGTGTCAGTGGGTACAGGGAGCGTGTGAGT GCATGTGAGTGTGTGTTAGAGTTACAGGGGTGGGCTGTGTCAGTGGGTACAGGGAGCGTGTGAGT T C RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82671980..82672430 26863196 MeRIP-seq:(Medium) rs28970460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5368810,Human_RBP_ID_17903613,Human_RBP_ID_23756681 101276 RMVar_ID_101276 Human_SNP_ID_634974144 m1A Human chr17 - 82697587 82697587 82697587 CTTCACCCACGCGCATCCCTGGAACAGCTTGGACGAGGCCGACCCTGAGGCTGTGGAAGGAGCCC CTTCACCCACGCGCATCCCTGGAACAGCTTGGGCGAGGCCGACCCTGAGGCTGTGGAAGGAGCCC T C RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82697585..82697936 26863196 MeRIP-seq:(Medium) rs1366188587 Functional Loss SNV dbSNP153 33..33 33 - - - 101277 RMVar_ID_101277 Human_SNP_ID_634980591 m1A Human chr17 - 82718060 82718060 82718060 ACACAACACACAGACACACACACACAACATACACAGCAGTGATCCCCGCAGAACAGGTCAGGGCC ACACAACACACAGACACACACACACAACATACTCAGCAGTGATCCCCGCAGAACAGGTCAGGGCC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82718009..82718180 26863196 MeRIP-seq:(Medium) rs928321394 Functional Loss SNV dbSNP153 33..33 33 - - - 101278 RMVar_ID_101278 Human_SNP_ID_634980860 m1A Human chr17 + 82718997 82718997 82718997 GGTGAAAGTGCCCAAGCCCATCAAGGTTCTGGATGCCCCAGGCGGCGGGAGCGTGCTGGTGATGG GGTGAAAGTGCCCAAGCCCATCAAGGTTCTGGGTGCCCCAGGCGGCGGGAGCGTGCTGGTGATGG A G FN3KRP Ensembl:ENSG00000141560 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82718843..82720796 26863196 MeRIP-seq:(Medium) rs369441626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7066,Human_RBP_ID_503950,Human_RBP_ID_9377193,Human_RBP_ID_18989784 Human_Splice_Rec_1886402,Human_Splice_Rec_1886403,Human_Splice_Rec_1886414,Human_Splice_Rec_1886415,Human_Splice_Rec_1886424,Human_Splice_Rec_1886425,Human_Splice_Rec_1886436,Human_Splice_Rec_1886437,Human_Splice_Rec_1886446,Human_Splice_Rec_1886447,Human_Splice_Rec_1886459 RMVar_hsa_circ_357305 101279 RMVar_ID_101279 Human_SNP_ID_634980861 m1A Human chr17 + 82718997 82718997 82718997 GGTGAAAGTGCCCAAGCCCATCAAGGTTCTGGATGCCCCAGGCGGCGGGAGCGTGCTGGTGATGG GGTGAAAGTGCCCAAGCCCATCAAGGTTCTGGTTGCCCCAGGCGGCGGGAGCGTGCTGGTGATGG A T FN3KRP Ensembl:ENSG00000141560 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82718843..82720796 26863196 MeRIP-seq:(Medium) rs369441626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7066,Human_RBP_ID_503950,Human_RBP_ID_9377193,Human_RBP_ID_18989784 Human_Splice_Rec_1886402,Human_Splice_Rec_1886403,Human_Splice_Rec_1886414,Human_Splice_Rec_1886415,Human_Splice_Rec_1886424,Human_Splice_Rec_1886425,Human_Splice_Rec_1886436,Human_Splice_Rec_1886437,Human_Splice_Rec_1886446,Human_Splice_Rec_1886447,Human_Splice_Rec_1886459 RMVar_hsa_circ_357305 101280 RMVar_ID_101280 Human_SNP_ID_634986200 m1A Human chr17 + 82735769 82735769 82735769 ACGCAGGCCCAGTGTTCGTCAAAGTCAACCGCAGGACGCAGGTGCTGGCCCGTGCGCAGGCGGGG ACGCAGGCCCAGTGTTCGTCAAAGTCAACCGCTGGACGCAGGTGCTGGCCCGTGCGCAGGCGGGG A T FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82735599..82736117 26863196 MeRIP-seq:(Medium) rs1424412284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9327082,Human_RBP_ID_19080781,Human_RBP_ID_26813015 Human_Splice_Rec_1886475,Human_Splice_Rec_1886485,Human_Splice_Rec_1886489 101281 RMVar_ID_101281 Human_SNP_ID_634986452 m1A Human chr17 + 82736617 82736617 82736617 AGCTTCAGCCTTGAGAGCCGGCAGGTGGAGAAAGGCAGGCCTGGGTGCCCTCCCGGCCCGAGTGG AGCTTCAGCCTTGAGAGCCGGCAGGTGGAGAATGGCAGGCCTGGGTGCCCTCCCGGCCCGAGTGG A T FN3K Ensembl:ENSG00000167363 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82736610..82736685 26863196 MeRIP-seq:(Medium) rs919227525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5368818,Human_RBP_ID_26758618 101282 RMVar_ID_101282 Human_SNP_ID_634987119 m1A Human chr17 + 82738567 82738567 82738567 GGAGCACGGGCCTGGTGCGGGTGCCGAGGCCCATGAAGGTCATCGACCTGCCGGGAGGTGGGGCC GGAGCACGGGCCTGGTGCGGGTGCCGAGGCCCGTGAAGGTCATCGACCTGCCGGGAGGTGGGGCC A G FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82738516..82738679 26863196 MeRIP-seq:(Medium) rs1158165810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542200,Human_RBP_ID_4467430,Human_RBP_ID_5318743,Human_RBP_ID_9379426,Human_RBP_ID_18989787,Human_RBP_ID_20292177 Human_Splice_Rec_1886476,Human_Splice_Rec_1886477,Human_Splice_Rec_1886486,Human_Splice_Rec_1886487,Human_Splice_Rec_1886490,Human_Splice_Rec_1886491,Human_Splice_Rec_1886497 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 101283 RMVar_ID_101283 Human_SNP_ID_634987140 m1A Human chr17 + 82738624 82738618 82738624 GTGGGGCCGCCTTTGTGATGGAGCATTTGAAGATGAAGAGCTTGAGCAGGTGAGTGTGTGTGAGA GTGGGGCCGCCTTTGTGATGGAGCATT______TGAAGAGCTTGAGCAGGTGAGTGTGTGTGAGA TTGAAGA T FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82738423..82738684 26863196 MeRIP-seq:(Medium) rs765051579 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_897170,Human_RBP_ID_3542200,Human_RBP_ID_4467430,Human_RBP_ID_9377197,Human_RBP_ID_9424504,Human_RBP_ID_18989788,Human_RBP_ID_26334019 Human_Splice_Rec_1886477,Human_Splice_Rec_1886487,Human_Splice_Rec_1886491,Human_Splice_Rec_1886497 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 101284 RMVar_ID_101284 Human_SNP_ID_634987853 m1A Human chr17 + 82740827 82740827 82740827 ATTTGCATCTTTACAACCAGAAGCTCAGGGAGAAGTTGAAGGAGGAGGAGAACACAGTGGGTATG ATTTGCATCTTTACAACCAGAAGCTCAGGGAGGAGTTGAAGGAGGAGGAGAACACAGTGGGTATG A G FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82740721..82740906 26863196 MeRIP-seq:(Medium) rs371202212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542202,Human_RBP_ID_3953411,Human_RBP_ID_9377198,Human_RBP_ID_18943815,Human_RBP_ID_22445840,Human_RBP_ID_26332653 Human_Splice_Rec_1886478,Human_Splice_Rec_1886479,Human_Splice_Rec_1886488,Human_Splice_Rec_1886492,Human_Splice_Rec_1886493,Human_Splice_Rec_1886498,Human_Splice_Rec_1886499 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 101285 RMVar_ID_101285 Human_SNP_ID_634987946 m1A Human chr17 + 82741273 82741273 82741273 TGCTCTGCTGAGGTCTGGCATTTAAGAGAAAGACAAACAGCTCCTTCAGGCCAAGGATCTCTGTC TGCTCTGCTGAGGTCTGGCATTTAAGAGAAAGCCAAACAGCTCCTTCAGGCCAAGGATCTCTGTC A C FN3K Ensembl:ENSG00000167363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82741270..82741372 26863196 MeRIP-seq:(Medium) rs775680229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 101286 RMVar_ID_101286 Human_SNP_ID_634988003 m1A Human chr17 + 82741392 82741392 82741392 CCACACGGTGACGTGCTGCGGCTTCATCCCGCAGGTGAGTGCCTGGGTGAGGGTGTTCCCTGATG CCACACGGTGACGTGCTGCGGCTTCATCCCGCGGGTGAGTGCCTGGGTGAGGGTGTTCCCTGATG A G FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82741362..82749038 32194978 MeRIP-seq:(Medium) rs1476280296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503971,Human_RBP_ID_5363366,Human_RBP_ID_18989791,Human_RBP_ID_19080782,Human_RBP_ID_22445223,Human_RBP_ID_27814414 Human_Splice_Rec_1886480,Human_Splice_Rec_1886481,Human_Splice_Rec_1886494,Human_Splice_Rec_1886500,Human_Splice_Rec_1886501 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 101287 RMVar_ID_101287 Human_SNP_ID_634990663 m1A Human chr17 - 82750772 82750769 82750773 GGGGAGACGGAGACGGGGACGGGGACAGGGGAAGGGAGGGCAGGGGCCGCTACTTGAGCAGCCTT GGGGAGACGGAGACGGGGACGGGGACAGGGG____GAGGGCAGGGGCCGCTACTTGAGCAGCCTT CCCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82750452..82751112 32194978 MeRIP-seq:(Medium) rs761712823 Functional Loss DEL dbSNP153 32..35 33 - - - 101288 RMVar_ID_101288 Human_SNP_ID_634990667 m1A Human chr17 - 82750772 82750772 82750772 GGGGAGACGGAGACGGGGACGGGGACAGGGGAAGGGAGGGCAGGGGCCGCTACTTGAGCAGCCTT GGGGAGACGGAGACGGGGACGGGGACAGGGGAGGGGAGGGCAGGGGCCGCTACTTGAGCAGCCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82750452..82751112 32194978 MeRIP-seq:(Medium) rs765049179 Functional Loss SNV dbSNP153 33..33 33 - - - 101289 RMVar_ID_101289 Human_SNP_ID_634990918 m1A Human chr17 - 82751103 82751090 82751103 GGGGACAGGGACAGGGGGGACGGGGACGGGGGACGGGGACGGGGGGACGGCGATGGGAGACGGGG GGGGACAGGGACAGGGGGGACGGGGACGGGGG_____________GACGGCGATGGGAGACGGGG CCCCCCGTCCCCGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82750726..82751200 26863196 MeRIP-seq:(Medium) rs1369680220 Functional Loss DEL dbSNP153 33..45 33 - - - 101290 RMVar_ID_101290 Human_SNP_ID_634990926 m1A Human chr17 - 82751103 82751097 82751104 GGGGACAGGGACAGGGGGGACGGGGACGGGGGACGGGGACGGGGGGACGGCGATGGGAGACGGGG GGGGACAGGGACAGGGGGGACGGGGACGGGG_______ACGGGGGGACGGCGATGGGAGACGGGG TCCCCGTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82750726..82751200 26863196 MeRIP-seq:(Medium) rs1402904888 Functional Loss DEL dbSNP153 32..38 33 - - - 101291 RMVar_ID_101291 Human_SNP_ID_634990934 m1A Human chr17 - 82751103 82751102 82751103 GGGGACAGGGACAGGGGGGACGGGGACGGGGGACGGGGACGGGGGGACGGCGATGGGAGACGGGG GGGGACAGGGACAGGGGGGACGGGGACGGGGG_CGGGGACGGGGGGACGGCGATGGGAGACGGGG GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82750726..82751200 26863196 MeRIP-seq:(Medium) rs1299080490 Functional Loss DEL dbSNP153 33..33 33 - - - 101292 RMVar_ID_101292 Human_SNP_ID_634990943 m1A Human chr17 - 82751103 82751103 82751103 GGGGACAGGGACAGGGGGGACGGGGACGGGGGACGGGGACGGGGGGACGGCGATGGGAGACGGGG GGGGACAGGGACAGGGGGGACGGGGACGGGGGGCGGGGACGGGGGGACGGCGATGGGAGACGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82750726..82751200 26863196 MeRIP-seq:(Medium) rs1347104167 Functional Loss SNV dbSNP153 33..33 33 - - - 101293 RMVar_ID_101293 Human_SNP_ID_634990944 m1A Human chr17 - 82751103 82751103 82751103 GGGGACAGGGACAGGGGGGACGGGGACGGGGGACGGGGACGGGGGGACGGCGATGGGAGACGGGG GGGGACAGGGACAGGGGGGACGGGGACGGGGGCCGGGGACGGGGGGACGGCGATGGGAGACGGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82750726..82751200 26863196 MeRIP-seq:(Medium) rs1347104167 Functional Loss SNV dbSNP153 33..33 33 - - - 101294 RMVar_ID_101294 Human_SNP_ID_634991467 m1A Human chr17 - 82751973 82751973 82751973 AAATACCGCGCGCGGGACGGCGCGTGCACTTGAGGACGCGAGCGGGCACGGGTCCCAAAGGCTCT AAATACCGCGCGCGGGACGGCGCGTGCACTTGCGGACGCGAGCGGGCACGGGTCCCAAAGGCTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82751922..82751991 26863196 MeRIP-seq:(Medium) rs1322080427 Functional Loss SNV dbSNP153 33..33 33 - - - 101295 RMVar_ID_101295 Human_SNP_ID_634991571 m1A Human chr17 + 82752159 82752159 82752159 TTTCGCGCTCTAGCGGAGTGGGATCTGCGAACACGTGAGGCGGGGGCGCGGTCCCCAGGCTGCCG TTTCGCGCTCTAGCGGAGTGGGATCTGCGAACTCGTGAGGCGGGGGCGCGGTCCCCAGGCTGCCG A T TBCD Ensembl:ENSG00000141556 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82752100..82752320 26863196 MeRIP-seq:(Medium) rs756186378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301249,Human_RBP_ID_503972,Human_RBP_ID_4465864,Human_RBP_ID_9289583,Human_RBP_ID_18989792,Human_RBP_ID_22225110 RMVar_hsa_circ_87293,RMVar_hsa_circ_187987 101296 RMVar_ID_101296 Human_SNP_ID_634991617 m1A Human chr17 + 82752231 82752229 82752232 CCTGAGCGACGAACCGGCCGCGGGCGGCCCCGAGGAGGAGGCGGAGGACGAGACACTGGCCTTTG CCTGAGCGACGAACCGGCCGCGGGCGGCCCC___GAGGAGGCGGAGGACGAGACACTGGCCTTTG CGAG C TBCD Ensembl:ENSG00000141556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr17:82752076..82752400;chr17:82752145..82752372 26863196 MeRIP-seq:(Medium) rs1209134139 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_9289583,Human_RBP_ID_18993179 RMVar_hsa_circ_87293,RMVar_hsa_circ_187987 101297 RMVar_ID_101297 Human_SNP_ID_634991622 m1A Human chr17 + 82752237 82752237 82752237 CGACGAACCGGCCGCGGGCGGCCCCGAGGAGGAGGCGGAGGACGAGACACTGGCCTTTGGCGCGG CGACGAACCGGCCGCGGGCGGCCCCGAGGAGGCGGCGGAGGACGAGACACTGGCCTTTGGCGCGG A C TBCD Ensembl:ENSG00000141556 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:82752153..82752303 26863196 MeRIP-seq:(Medium) rs761196902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9289583 RMVar_hsa_circ_87293,RMVar_hsa_circ_187987 101298 RMVar_ID_101298 Human_SNP_ID_634992494 m1A Human chr17 + 82754775 82754775 82754775 GGCAGTTTTGCTGGGAAGCAGTGGGTGTGTTCAGATGTGGAGGTGGGAGCTGCCGGATTGGACAG GGCAGTTTTGCTGGGAAGCAGTGGGTGTGTTCCGATGTGGAGGTGGGAGCTGCCGGATTGGACAG A C TBCD Ensembl:ENSG00000141556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82754773..82754896 26863196 MeRIP-seq:(Medium) rs568933295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13210189 RMVar_hsa_circ_87293,RMVar_hsa_circ_187987 101299 RMVar_ID_101299 Human_SNP_ID_634992495 m1A Human chr17 + 82754775 82754775 82754775 GGCAGTTTTGCTGGGAAGCAGTGGGTGTGTTCAGATGTGGAGGTGGGAGCTGCCGGATTGGACAG GGCAGTTTTGCTGGGAAGCAGTGGGTGTGTTCGGATGTGGAGGTGGGAGCTGCCGGATTGGACAG A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82754773..82754896 26863196 MeRIP-seq:(Medium) rs568933295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13210189 RMVar_hsa_circ_87293,RMVar_hsa_circ_187987 101300 RMVar_ID_101300 Human_SNP_ID_635006317 m1A Human chr17 - 82801869 82801826 82801869 CCACGCTGACTCCGAACCACACGACGCACACGACGCCCTCCTGCCACGCTGACTCCGAACCACAC CCACGCTGACTCCGAACCACACGACGCACACG_________________________________ GCGTGTGCGTCGTGTGGTTCGGAGTCAGCGTGGCAGGAGGGCGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82801862..82801945 26863196 MeRIP-seq:(Medium) rs766951348 Functional Loss DEL dbSNP153 33..65 33 - - - 101301 RMVar_ID_101301 Human_SNP_ID_635006340 m1A Human chr17 - 82801869 82801869 82801869 CCACGCTGACTCCGAACCACACGACGCACACGACGCCCTCCTGCCACGCTGACTCCGAACCACAC CCACGCTGACTCCGAACCACACGACGCACACGCCGCCCTCCTGCCACGCTGACTCCGAACCACAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82801862..82801945 26863196 MeRIP-seq:(Medium) rs1311657767 Functional Loss SNV dbSNP153 33..33 33 - - - 101302 RMVar_ID_101302 Human_SNP_ID_635008817 m1A Human chr17 + 82809715 82809715 82809715 ACGGATTGCTGCGTTTCTCTTTCAGCATCGGTAGGATGGCTGGCAGGCTTCCCAGAGCCCTGGCG ACGGATTGCTGCGTTTCTCTTTCAGCATCGGTGGGATGGCTGGCAGGCTTCCCAGAGCCCTGGCG A G TBCD Ensembl:ENSG00000141556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82809701..82809800 26863196 MeRIP-seq:(Medium) rs901666996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904625,Human_RBP_ID_3951539,Human_RBP_ID_8232529,Human_RBP_ID_9290489,Human_RBP_ID_18989801,Human_RBP_ID_27838682 Human_Splice_Rec_1886524,Human_Splice_Rec_1886525,Human_Splice_Rec_1886600,Human_Splice_Rec_1886601 RMVar_hsa_circ_188013,RMVar_hsa_circ_126026,RMVar_hsa_circ_76635,RMVar_hsa_circ_280363,RMVar_hsa_circ_87293,RMVar_hsa_circ_332008,RMVar_hsa_circ_347826,RMVar_hsa_circ_187987,RMVar_hsa_circ_332781,RMVar_hsa_circ_323059,RMVar_hsa_circ_291982,RMVar_hsa_circ_298521,RMVar_hsa_circ_97182,RMVar_hsa_circ_270369,RMVar_hsa_circ_93164,RMVar_hsa_circ_95201,RMVar_hsa_circ_87524,RMVar_hsa_circ_187991,RMVar_hsa_circ_187995,RMVar_hsa_circ_187997,RMVar_hsa_circ_187996,RMVar_hsa_circ_187993,RMVar_hsa_circ_187994,RMVar_hsa_circ_187992,RMVar_hsa_circ_281096,RMVar_hsa_circ_187989,RMVar_hsa_circ_187990,RMVar_hsa_circ_187988,RMVar_hsa_circ_312530,RMVar_hsa_circ_318849,RMVar_hsa_circ_376231,RMVar_hsa_circ_285468,RMVar_hsa_circ_271180,RMVar_hsa_circ_270486,RMVar_hsa_circ_270811,RMVar_hsa_circ_93941,RMVar_hsa_circ_106981,RMVar_hsa_circ_110214,RMVar_hsa_circ_120959,RMVar_hsa_circ_104584,RMVar_hsa_circ_105285,RMVar_hsa_circ_101731,RMVar_hsa_circ_79065,RMVar_hsa_circ_84459,RMVar_hsa_circ_89285,RMVar_hsa_circ_81315,RMVar_hsa_circ_188029,RMVar_hsa_circ_188031,RMVar_hsa_circ_78452,RMVar_hsa_circ_188032,RMVar_hsa_circ_188030,RMVar_hsa_circ_188027,RMVar_hsa_circ_188028,RMVar_hsa_circ_188017,RMVar_hsa_circ_188018,RMVar_hsa_circ_188015,RMVar_hsa_circ_188016,RMVar_hsa_circ_188014,RMVar_hsa_circ_23610,RMVar_hsa_circ_108590,RMVar_hsa_circ_188009,RMVar_hsa_circ_188011,RMVar_hsa_circ_188012,RMVar_hsa_circ_188010,RMVar_hsa_circ_188007,RMVar_hsa_circ_188008,RMVar_hsa_circ_188006,RMVar_hsa_circ_105752,RMVar_hsa_circ_98417,RMVar_hsa_circ_188037,RMVar_hsa_circ_188039,RMVar_hsa_circ_82578,RMVar_hsa_circ_188038,RMVar_hsa_circ_188044,RMVar_hsa_circ_89869,RMVar_hsa_circ_188036,RMVar_hsa_circ_356166,RMVar_hsa_circ_97909,RMVar_hsa_circ_124670,RMVar_hsa_circ_98772,RMVar_hsa_circ_188049,RMVar_hsa_circ_353372,RMVar_hsa_circ_358308,RMVar_hsa_circ_371015,RMVar_hsa_circ_348250,RMVar_hsa_circ_109124,RMVar_hsa_circ_188051,RMVar_hsa_circ_188053,RMVar_hsa_circ_188054,RMVar_hsa_circ_188052,RMVar_hsa_circ_188050,RMVar_hsa_circ_372565,RMVar_hsa_circ_107218,RMVar_hsa_circ_188058,RMVar_hsa_circ_188059,RMVar_hsa_circ_188057,RMVar_hsa_circ_188062,RMVar_hsa_circ_301692,RMVar_hsa_circ_371463,RMVar_hsa_circ_345038,RMVar_hsa_circ_188060,RMVar_hsa_circ_188061,RMVar_hsa_circ_103292,RMVar_hsa_circ_188067,RMVar_hsa_circ_188064,RMVar_hsa_circ_188066,RMVar_hsa_circ_86361,RMVar_hsa_circ_188065,RMVar_hsa_circ_107320 101303 RMVar_ID_101303 Human_SNP_ID_635021081 m1A Human chr17 - 82849151 82849137 82849152 GCAGCAGGCAGAGGGGGACATCGAGATGGAGAAGACGCAGCAGGCAGAGGGGAACATCGAGGTGG GCAGCAGGCAGAGGGGGACATCGAGATGGAG_______________GAGGGGAACATCGAGGTGG CTGCCTGCTGCGTCTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82849147..82849244 26863196 MeRIP-seq:(Medium) rs1555614312 Functional Loss DEL dbSNP153 32..46 33 - - - 101304 RMVar_ID_101304 Human_SNP_ID_635027001 m1A Human chr17 + 82868020 82868020 82868020 AGGGAACGCAGAGCTGCCGTGTGTGGCCGTGCAGGGCCTTCCACAGTGAGTTGTGGGGTCCTGGG AGGGAACGCAGAGCTGCCGTGTGTGGCCGTGCGGGGCCTTCCACAGTGAGTTGTGGGGTCCTGGG A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82868019..82868180 26863196 MeRIP-seq:(Medium) rs1164006630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7072,Human_RBP_ID_24371555 RMVar_hsa_circ_188013,RMVar_hsa_circ_126026,RMVar_hsa_circ_76635,RMVar_hsa_circ_87293,RMVar_hsa_circ_332008,RMVar_hsa_circ_347826,RMVar_hsa_circ_187987,RMVar_hsa_circ_332781,RMVar_hsa_circ_323059,RMVar_hsa_circ_291982,RMVar_hsa_circ_298521,RMVar_hsa_circ_97182,RMVar_hsa_circ_93164,RMVar_hsa_circ_95201,RMVar_hsa_circ_87524,RMVar_hsa_circ_187991,RMVar_hsa_circ_187995,RMVar_hsa_circ_187996,RMVar_hsa_circ_187993,RMVar_hsa_circ_187994,RMVar_hsa_circ_187992,RMVar_hsa_circ_281096,RMVar_hsa_circ_187989,RMVar_hsa_circ_187990,RMVar_hsa_circ_187988,RMVar_hsa_circ_312530,RMVar_hsa_circ_318849,RMVar_hsa_circ_376231,RMVar_hsa_circ_271180,RMVar_hsa_circ_270811,RMVar_hsa_circ_93941,RMVar_hsa_circ_106981,RMVar_hsa_circ_110214,RMVar_hsa_circ_120959,RMVar_hsa_circ_104584,RMVar_hsa_circ_101731,RMVar_hsa_circ_79065,RMVar_hsa_circ_84459,RMVar_hsa_circ_89285,RMVar_hsa_circ_81315,RMVar_hsa_circ_188031,RMVar_hsa_circ_78452,RMVar_hsa_circ_188032,RMVar_hsa_circ_188030,RMVar_hsa_circ_188017,RMVar_hsa_circ_188018,RMVar_hsa_circ_188015,RMVar_hsa_circ_188016,RMVar_hsa_circ_188014,RMVar_hsa_circ_108590,RMVar_hsa_circ_188009,RMVar_hsa_circ_188011,RMVar_hsa_circ_188012,RMVar_hsa_circ_188010,RMVar_hsa_circ_188007,RMVar_hsa_circ_188008,RMVar_hsa_circ_188006,RMVar_hsa_circ_105752,RMVar_hsa_circ_98417,RMVar_hsa_circ_188037,RMVar_hsa_circ_188039,RMVar_hsa_circ_82578,RMVar_hsa_circ_188038,RMVar_hsa_circ_188036,RMVar_hsa_circ_97909,RMVar_hsa_circ_124670,RMVar_hsa_circ_98772,RMVar_hsa_circ_371015,RMVar_hsa_circ_348250,RMVar_hsa_circ_109124,RMVar_hsa_circ_188051,RMVar_hsa_circ_188053,RMVar_hsa_circ_188052,RMVar_hsa_circ_188050,RMVar_hsa_circ_107218,RMVar_hsa_circ_188058,RMVar_hsa_circ_188059,RMVar_hsa_circ_371463,RMVar_hsa_circ_188060,RMVar_hsa_circ_103292,RMVar_hsa_circ_188068,RMVar_hsa_circ_94381,RMVar_hsa_circ_188067,RMVar_hsa_circ_188064,RMVar_hsa_circ_188066,RMVar_hsa_circ_86361,RMVar_hsa_circ_188065,RMVar_hsa_circ_107320,RMVar_hsa_circ_335004,RMVar_hsa_circ_342664,RMVar_hsa_circ_347109,RMVar_hsa_circ_336455,RMVar_hsa_circ_322460,RMVar_hsa_circ_188070,RMVar_hsa_circ_52004,RMVar_hsa_circ_188071,RMVar_hsa_circ_188069 101305 RMVar_ID_101305 Human_SNP_ID_635027199 m1A Human chr17 - 82868883 82868883 82868883 CACACGACCCGCTCCACGCACACGCCGTCTGTACACTTCACACCCACCAATCAAGTTCACTAACA CACACGACCCGCTCCACGCACACGCCGTCTGTTCACTTCACACCCACCAATCAAGTTCACTAACA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82868879..82869027 26863196 MeRIP-seq:(Medium) rs904507169 Functional Loss SNV dbSNP153 33..33 33 - - - 101306 RMVar_ID_101306 Human_SNP_ID_635049348 m1A Human chr17 - 82939475 82939475 82939475 AGGTGGCCGTGCAGGAAGGGCCTTCACTCACCACGCAGTGTCACTGAGCACAGTCACCACCTCGT AGGTGGCCGTGCAGGAAGGGCCTTCACTCACCTCGCAGTGTCACTGAGCACAGTCACCACCTCGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82939428..82939501 26863196 MeRIP-seq:(Medium) rs1568106593 Functional Loss SNV dbSNP153 33..33 33 - - - 101307 RMVar_ID_101307 Human_SNP_ID_635055129 m1A Human chr17 + 82957937 82957937 82957937 GTCGCTGCCCCGAACCCTTCCACTCCCCTGGGAACCTGGTCTCTGTTCTCCCTCTGCTGTGACAA GTCGCTGCCCCGAACCCTTCCACTCCCCTGGGGACCTGGTCTCTGTTCTCCCTCTGCTGTGACAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82957933..82958064 26863196 MeRIP-seq:(Medium) rs1360670248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62407,RMVar_hsa_circ_296276,RMVar_hsa_circ_50873 101308 RMVar_ID_101308 Human_SNP_ID_635055141 m1A Human chr17 + 82957969 82957969 82957969 AACCTGGTCTCTGTTCTCCCTCTGCTGTGACAAGTCGACCCCAGGCTGCTGTCCCGGGGGGAGCA AACCTGGTCTCTGTTCTCCCTCTGCTGTGACAGGTCGACCCCAGGCTGCTGTCCCGGGGGGAGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82957920..82958101 26863196 MeRIP-seq:(Medium) rs575880410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62407,RMVar_hsa_circ_296276,RMVar_hsa_circ_50873 101309 RMVar_ID_101309 Human_SNP_ID_635080269 m1A Human chr17 - 83039608 83039608 83039608 GGCGGGCAGCGGGCGCCCAGCAGTGTGTCTAGAACAGGGGCGGGCGGTGGGCGCCCAGCAGTGTG GGCGGGCAGCGGGCGCCCAGCAGTGTGTCTAGGACAGGGGCGGGCGGTGGGCGCCCAGCAGTGTG T C B3GNTL1 Ensembl:ENSG00000175711 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:83039527..83039614 26863196 MeRIP-seq:(Medium) rs1452494012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72744,RMVar_hsa_circ_268142,RMVar_hsa_circ_188157,RMVar_hsa_circ_366977 101310 RMVar_ID_101310 Human_SNP_ID_635092954 m1A Human chr17 + 83079713 83079713 83079713 CGCGGAGGACGCGGGGGGCGCGCGACGTGACCACCCGGACTCGAAGCCCGCCCCGCCCCCGCCCG CGCGGAGGACGCGGGGGGCGCGCGACGTGACCCCCCGGACTCGAAGCCCGCCCCGCCCCCGCCCG A C METRNL Ensembl:ENSG00000176845 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:83079617..83079875;chr17:83079629..83079847 26863410 MeRIP-seq:(Medium) rs952460793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27459804 101311 RMVar_ID_101311 Human_SNP_ID_635093002 m1A Human chr17 - 83079840 83079840 83079840 GGGTCGCGGCCACGGCTGCCCCGCGCGCCCCCAGGCCGCCCGCGCCGCGCCCCGCATGCTCTGGC GGGTCGCGGCCACGGCTGCCCCGCGCGCCCCCCGGCCGCCCGCGCCGCGCCCCGCATGCTCTGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:83079685..83079935 26863196 MeRIP-seq:(Medium) rs1239074924 Functional Loss SNV dbSNP153 33..33 33 - - - 101312 RMVar_ID_101312 Human_SNP_ID_635095017 m1A Human chr17 + 83085192 83085192 83085192 ACCAGACGGGGACGGCAGGCCCGGCCGGGTGCAGTGTTTTGGCCTGGAGCAGGGCGGCCTGTTCG ACCAGACGGGGACGGCAGGCCCGGCCGGGTGCGGTGTTTTGGCCTGGAGCAGGGCGGCCTGTTCG A G METRNL Ensembl:ENSG00000176845 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:83085012..83085251 26863196 MeRIP-seq:(Medium) rs75438321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17903713 RMVar_hsa_circ_295038 101313 RMVar_ID_101313 Human_SNP_ID_635098727 m1A Human chr17 - 83094684 83094684 83094684 ACAGCTTCGGTACCAGGGTCAGGCCTGGGCCCAGGGCATGCGGCTCCCAGCGCGCGGCCCTCACC ACAGCTTCGGTACCAGGGTCAGGCCTGGGCCCGGGGCATGCGGCTCCCAGCGCGCGGCCCTCACC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:83084926..83094800 32194978 MeRIP-seq:(Medium) rs1157444622 Functional Loss SNV dbSNP153 33..33 33 - - - 101314 RMVar_ID_101314 Human_SNP_ID_635101203 m1A Human chr17 - 83101247 83101247 83101247 AGCTCGGCTCGGCCCCACGGCACGGGAGAGGCAGAAGCTCCAGCAGTGAGTTCTCCCTGAGCTGC AGCTCGGCTCGGCCCCACGGCACGGGAGAGGCGGAAGCTCCAGCAGTGAGTTCTCCCTGAGCTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:83101010..83101347 32194978 MeRIP-seq:(Medium) rs1441363575 Functional Loss SNV dbSNP153 33..33 33 - - - 101315 RMVar_ID_101315 Human_SNP_ID_495571881 m1A Human chr12 - 30629601 30629601 30629601 TTTATTCAGCAAAATGAAAACGTATCTTCAGAACTTAACATATTACTGGATGTGATACAGATTTT TTTATTCAGCAAAATGAAAACGTATCTTCAGAGCTTAACATATTACTGGATGTGATACAGATTTT T C IPO8 Ensembl:ENSG00000133704 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs75560605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17470546 RMVar_hsa_circ_268889 101316 RMVar_ID_101316 Human_SNP_ID_495572556 m1A Human chr12 - 30632510 30632509 30632510 GGAGACTAATAGAACTGGTGAGATAAATGGAGAGATAGAAGGTTTGGGAGGAAATTGTTAAATTT GGAGACTAATAGAACTGGTGAGATAAATGGAG_GATAGAAGGTTTGGGAGGAAATTGTTAAATTT CT C IPO8 Ensembl:ENSG00000133704 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:30632459..30632698 26863196 MeRIP-seq:(Medium) rs778326151 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23555792 RMVar_hsa_circ_88613,RMVar_hsa_circ_268889,RMVar_hsa_circ_155603 101317 RMVar_ID_101317 Human_SNP_ID_495572878 m1A Human chr12 - 30634124 30634124 30634124 TGAGGGGTTCAGTACTCCACTTGACCTTGACAATAGTGTGGATGAATATCAGTTTTTTACACAAG TGAGGGGTTCAGTACTCCACTTGACCTTGACAGTAGTGTGGATGAATATCAGTTTTTTACACAAG T C IPO8 Ensembl:ENSG00000133704 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:30634076..30634125 32194978 MeRIP-seq:(Medium) rs568068681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_195275,Human_RBP_ID_2331373,Human_RBP_ID_11921115,Human_RBP_ID_22173264,Human_RBP_ID_23555795,Human_RBP_ID_26321268,Human_RBP_ID_27805332 Human_Splice_Rec_1351285,Human_Splice_Rec_1351325,Human_Splice_Rec_1351331 RMVar_hsa_circ_88613,RMVar_hsa_circ_268889,RMVar_hsa_circ_155603 101318 RMVar_ID_101318 Human_SNP_ID_495586867 m1A Human chr12 - 30695732 30695732 30695732 GGGTGGGGTGTGAGGTAATCCAGGGGTCGCGGAAGAGGAGGCTGAGAGGGTCAAAAGAAAACTAA GGGTGGGGTGTGAGGTAATCCAGGGGTCGCGGGAGAGGAGGCTGAGAGGGTCAAAAGAAAACTAA T C IPO8 Ensembl:ENSG00000133704 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:30695586..30695875;chr12:30695618..30695875 26863196 MeRIP-seq:(Medium) rs1346568968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115890,Human_RBP_ID_755650,Human_RBP_ID_2331468,Human_RBP_ID_3941479,Human_RBP_ID_4248108,Human_RBP_ID_5139835,Human_RBP_ID_5170858,Human_RBP_ID_5314521,Human_RBP_ID_8179039,Human_RBP_ID_8229603,Human_RBP_ID_9416398,Human_RBP_ID_18417246,Human_RBP_ID_26321272 101319 RMVar_ID_101319 Human_SNP_ID_495586897 m1A Human chr12 - 30695823 30695808 30695824 GGAGAGCGAGTTGTGGGGGGGAAAAAGGGAGGACAGGGGGCGCGGAGTCAGAGTGGCGCAGCAAG GGAGAGCGAGTTGTGGGGGGGAAAAAGGGAG________________TCAGAGTGGCGCAGCAAG ACTCCGCGCCCCCTGTC A IPO8 Ensembl:ENSG00000133704 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:30695626..30695875 26863196 MeRIP-seq:(Medium) rs1415385604 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_4254125,Human_RBP_ID_18417247 101320 RMVar_ID_101320 Human_SNP_ID_495590411 m1A Human chr12 - 30709719 30709719 30709719 GTGAAAAATCAAGCTGAATGACAATTAGCACTAATCTGGCACTTTATAAATTGTGATGTAGCCTC GTGAAAAATCAAGCTGAATGACAATTAGCACTTATCTGGCACTTTATAAATTGTGATGTAGCCTC T A CAPRIN2 Ensembl:ENSG00000110888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111681,Human_RBP_ID_6174339,Human_RBP_ID_18160168 Human_miRNA_ID_778970,Human_miRNA_ID_1751051,Human_miRNA_ID_1942745,Human_miRNA_ID_1945791,Human_miRNA_ID_2063351,Human_miRNA_ID_2116936,Human_miRNA_ID_2200514,Human_miRNA_ID_2203578,Human_miRNA_ID_2448720,Human_miRNA_ID_2816039,Human_miRNA_ID_2863302,Human_miRNA_ID_2901015,Human_miRNA_ID_3113031 RMVar_hsa_circ_155622,RMVar_hsa_circ_99386 101321 RMVar_ID_101321 Human_SNP_ID_495601261 m1A Human chr12 - 30753557 30753557 30753557 CAACTCTTTTCATCCCCTTTTGGTTACCAGTCACCTTCAGGCCATTCAGAGGAGGAAAGAGAGGG CAACTCTTTTCATCCCCTTTTGGTTACCAGTCGCCTTCAGGCCATTCAGAGGAGGAAAGAGAGGG T C CAPRIN2 Ensembl:ENSG00000110888 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:30753510..30753596 26863196 MeRIP-seq:(Medium) rs756390827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9364793,Human_RBP_ID_22538569,Human_RBP_ID_25015458 Human_Splice_Rec_1351666,Human_Splice_Rec_1351674,Human_Splice_Rec_1351682 RMVar_hsa_circ_275424,RMVar_hsa_circ_22895,RMVar_hsa_circ_155628,RMVar_hsa_circ_308222,RMVar_hsa_circ_355418,RMVar_hsa_circ_36436,RMVar_hsa_circ_37868,RMVar_hsa_circ_277336,RMVar_hsa_circ_155640,RMVar_hsa_circ_12588 101322 RMVar_ID_101322 Human_SNP_ID_495601262 m1A Human chr12 + 30753559 30753558 30753560 CTCTCTTTCCTCCTCTGAATGGCCTGAAGGTGACTGGTAACCAAAAGGGGATGAAAAGAGTTGCA CTCTCTTTCCTCCTCTGAATGGCCTGAAGGTG__TGGTAACCAAAAGGGGATGAAAAGAGTTGCA GAC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:30753515..30753621 26863196 MeRIP-seq:(Medium) rs779263012 Functional Loss DEL dbSNP153 33..34 33 - - - 101323 RMVar_ID_101323 Human_SNP_ID_495601639 m1A Human chr12 + 30754724 30754724 30754724 CGCCGGGTCAGCCGCCTCCCTCCGCCGCGCCGACCGAGGCCGCCGCAGCCCGACTTCACCTCCCC CGCCGGGTCAGCCGCCTCCCTCCGCCGCGCCGCCCGAGGCCGCCGCAGCCCGACTTCACCTCCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:30754349..30754938 26863196 MeRIP-seq:(Medium) rs1232241362 Functional Loss SNV dbSNP153 33..33 33 - - - 101324 RMVar_ID_101324 Human_SNP_ID_495676746 m1A Human chr12 - 31073999 31073999 31073999 CCTTCCTCGTCCCGCTGCTCCTCGTCCTAAGGAGCTCTGCTGCCACACAGCACTGCGCTCACCTT CCTTCCTCGTCCCGCTGCTCCTCGTCCTAAGGTGCTCTGCTGCCACACAGCACTGCGCTCACCTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:31073894..31074075;chr12:31073891..31074030;chr12:31073894..31074222;chr12:31073892..31074021 26863196 MeRIP-seq:(Medium) rs1445770991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18625069 101325 RMVar_ID_101325 Human_SNP_ID_495679797 m1A Human chr12 + 31085051 31085051 31085051 GCTAGAGACAGGCCCGGAGGCTGAGCGGCTGGAGCAGCTGGAGTCTGGGGAGGAGGAGCTGGTCC GCTAGAGACAGGCCCGGAGGCTGAGCGGCTGGGGCAGCTGGAGTCTGGGGAGGAGGAGCTGGTCC A G DDX11 Ensembl:ENSG00000013573 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:31085001..31085166 26863196 MeRIP-seq:(Medium) rs759585355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228369,Human_RBP_ID_809408,Human_RBP_ID_874371,Human_RBP_ID_5348206,Human_RBP_ID_9364796,Human_RBP_ID_18976922,Human_RBP_ID_22910980,Human_RBP_ID_26321275,Human_RBP_ID_27805350 Human_Splice_Rec_1351872,Human_Splice_Rec_1351873,Human_Splice_Rec_1351894,Human_Splice_Rec_1351895,Human_Splice_Rec_1351946,Human_Splice_Rec_1351947,Human_Splice_Rec_1351996,Human_Splice_Rec_1351997,Human_Splice_Rec_1352012,Human_Splice_Rec_1352013,Human_Splice_Rec_1352064,Human_Splice_Rec_1352065,Human_Splice_Rec_1352082,Human_Splice_Rec_1352083,Human_Splice_Rec_1352124,Human_Splice_Rec_1352125,Human_Splice_Rec_1352174,Human_Splice_Rec_1352175,Human_Splice_Rec_1352186,Human_Splice_Rec_1352187,Human_Splice_Rec_1352238,Human_Splice_Rec_1352239,Human_Splice_Rec_1352288,Human_Splice_Rec_1352289,Human_Splice_Rec_1352300,Human_Splice_Rec_1352310,Human_Splice_Rec_1352311 Human_miRNA_ID_2257662,Human_miRNA_ID_2974014,Human_miRNA_ID_3007202 RMVar_hsa_circ_74755,RMVar_hsa_circ_360582,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101326 RMVar_ID_101326 Human_SNP_ID_495679835 m1A Human chr12 + 31085125 31085125 31085125 ACGAGAGTGATGAGGAGAAAAAGGTGGCGAGCAGGTGAGACAGAGGCGGTAGCACTACCCTGCCC ACGAGAGTGATGAGGAGAAAAAGGTGGCGAGCGGGTGAGACAGAGGCGGTAGCACTACCCTGCCC A G DDX11 Ensembl:ENSG00000013573 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2536756 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_809409,Human_RBP_ID_872197,Human_RBP_ID_18976923,Human_RBP_ID_22572313,Human_RBP_ID_26321276 Human_Splice_Rec_1351873,Human_Splice_Rec_1351895,Human_Splice_Rec_1351947,Human_Splice_Rec_1351997,Human_Splice_Rec_1352013,Human_Splice_Rec_1352065,Human_Splice_Rec_1352083,Human_Splice_Rec_1352125,Human_Splice_Rec_1352175,Human_Splice_Rec_1352187,Human_Splice_Rec_1352239,Human_Splice_Rec_1352289,Human_Splice_Rec_1352311 RMVar_hsa_circ_74755,RMVar_hsa_circ_360582,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101327 RMVar_ID_101327 Human_SNP_ID_495679838 m1A Human chr12 - 31085128 31085128 31085128 CTGGGGCAGGGTAGTGCTACCGCCTCTGTCTCACCTGCTCGCCACCTTTTTCTCCTCATCACTCT CTGGGGCAGGGTAGTGCTACCGCCTCTGTCTCCCCTGCTCGCCACCTTTTTCTCCTCATCACTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:31085001..31085170;chr12:31085001..31086065;chr12:31085012..31085182 26863196 MeRIP-seq:(Medium) rs759356272 Functional Loss SNV dbSNP153 33..33 33 - - - 101328 RMVar_ID_101328 Human_SNP_ID_495680525 m1A Human chr12 + 31087892 31087892 31087892 AGCGCTCAGCAGATGCTCAGTGCGTTTTGCTGAGTTTGCTGAGGGAAGACTGTTTTCTGTTCTCT AGCGCTCAGCAGATGCTCAGTGCGTTTTGCTGGGTTTGCTGAGGGAAGACTGTTTTCTGTTCTCT A G DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:31087890..31088025 26863196 MeRIP-seq:(Medium) rs1171826882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101329 RMVar_ID_101329 Human_SNP_ID_495680542 m1A Human chr12 + 31087928 31087924 31087928 TGCTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACC TGCTGAGGGAAGACTGTTTTCTGTTCTCT____CACACACAGAGTGGATGAGGATGAGGATGACC TCTCA T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31087926..31088000 26863196 MeRIP-seq:(Medium) rs781143980 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101330 RMVar_ID_101330 Human_SNP_ID_495680545 m1A Human chr12 + 31087930 31087926 31087930 CTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACCTG CTGAGGGAAGACTGTTTTCTGTTCTCTCT____CACACAGAGTGGATGAGGATGAGGATGACCTG TCACA T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31087926..31089136 26863196 MeRIP-seq:(Medium) rs540967416 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101331 RMVar_ID_101331 Human_SNP_ID_495680546 m1A Human chr12 + 31087930 31087926 31087930 CTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACCTG CTGAGGGAAGACTGTTTTCTGTTCTCTCTCA__CACACAGAGTGGATGAGGATGAGGATGACCTG TCACA TCA DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31087926..31089136 26863196 MeRIP-seq:(Medium) rs540967416 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101332 RMVar_ID_101332 Human_SNP_ID_495680550 m1A Human chr12 + 31087928 31087928 31087928 TGCTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACC TGCTGAGGGAAGACTGTTTTCTGTTCTCTCTCTCACACACAGAGTGGATGAGGATGAGGATGACC A T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31087926..31088000 26863196 MeRIP-seq:(Medium) rs7308754 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101333 RMVar_ID_101333 Human_SNP_ID_495680552 m1A Human chr12 + 31087930 31087930 31087930 CTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACCTG CTGAGGGAAGACTGTTTTCTGTTCTCTCTCACTCACACAGAGTGGATGAGGATGAGGATGACCTG A T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31087926..31089136 26863196 MeRIP-seq:(Medium) rs752835521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101334 RMVar_ID_101334 Human_SNP_ID_495680554 m1A Human chr12 + 31087932 31087932 31087932 GAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACCTGGA GAGGGAAGACTGTTTTCTGTTCTCTCTCACACGCACAGAGTGGATGAGGATGAGGATGACCTGGA A G DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:31087926..31088000 26863196 MeRIP-seq:(Medium) rs555397858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101335 RMVar_ID_101335 Human_SNP_ID_495680555 m1A Human chr12 + 31087932 31087932 31087932 GAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACCTGGA GAGGGAAGACTGTTTTCTGTTCTCTCTCACACTCACAGAGTGGATGAGGATGAGGATGACCTGGA A T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:31087926..31088000 26863196 MeRIP-seq:(Medium) rs555397858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 101336 RMVar_ID_101336 Human_SNP_ID_495681058 m1A Human chr12 - 31089465 31089465 31089465 TGGCTACCGTGCCTGCTTCTCTGCATGTCCACACAGCGGTCGTTGATAAGCTGCACAGAACCTAG TGGCTACCGTGCCTGCTTCTCTGCATGTCCACGCAGCGGTCGTTGATAAGCTGCACAGAACCTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31089459..31089610 26863196 MeRIP-seq:(Medium) rs3881298 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_13237,GWAS_ID_13238,GWAS_ID_13239,GWAS_ID_13240,GWAS_ID_13241 101337 RMVar_ID_101337 Human_SNP_ID_495681075 m1A Human chr12 - 31089499 31089499 31089499 CTCCAGACCACCTGCGGCTACACCATGGTCCCAGTGGCTACCGTGCCTGCTTCTCTGCATGTCCA CTCCAGACCACCTGCGGCTACACCATGGTCCCGGTGGCTACCGTGCCTGCTTCTCTGCATGTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31089475..31089654 26863196 MeRIP-seq:(Medium) rs4031316 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 101338 RMVar_ID_101338 Human_SNP_ID_495681080 m1A Human chr12 + 31089506 31089506 31089506 GCAGAGAAGCAGGCACGGTAGCCACTGGGACCATGGTGTAGCCGCAGGTGGTCTGGAGAGAGTGA GCAGAGAAGCAGGCACGGTAGCCACTGGGACCGTGGTGTAGCCGCAGGTGGTCTGGAGAGAGTGA A G DDX11 Ensembl:ENSG00000013573 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2075318 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_809413,Human_RBP_ID_872198,Human_RBP_ID_1268792,Human_RBP_ID_3941489,Human_RBP_ID_19056005,Human_RBP_ID_26322758 GWAS_ID_13242,GWAS_ID_13243,GWAS_ID_13244,GWAS_ID_13245,GWAS_ID_13246 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643,RMVar_hsa_circ_25568 101339 RMVar_ID_101339 Human_SNP_ID_495683491 m1A Human chr12 - 31097212 31097212 31097212 CCCAGCTCCTCGATCTCCTCCCGTCCACCTCCACTGCTTACCCTGGTCACGGGACCCCCATCCCA CCCAGCTCCTCGATCTCCTCCCGTCCACCTCCGCTGCTTACCCTGGTCACGGGACCCCCATCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31097161..31097308 26863196 MeRIP-seq:(Medium) rs1242291172 Functional Loss SNV dbSNP153 33..33 33 - - - 101340 RMVar_ID_101340 Human_SNP_ID_495685730 m1A Human chr12 - 31103683 31103683 31103683 ATGGCGGGGCCAAAGGTAGCTTTGACCTCCACACGGGCTCGGATCCAGGCCGGCAGCTTGGCCAG ATGGCGGGGCCAAAGGTAGCTTTGACCTCCACGCGGGCTCGGATCCAGGCCGGCAGCTTGGCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr12:31103633..31103732;chr12:31103594..31103695 26863196,32194978 MeRIP-seq:(Medium) rs781237110 Functional Loss SNV dbSNP153 33..33 33 - - - 101341 RMVar_ID_101341 Human_SNP_ID_495685823 m1A Human chr12 + 31103893 31103892 31103894 GCCGTGCCCTTCCTTTGTCCTGCCCGCTGGAGACAGTGTTTGTCGTGGGCGTGGTCTGCGGGGAT GCCGTGCCCTTCCTTTGTCCTGCCCGCTGGAG__AGTGTTTGTCGTGGGCGTGGTCTGCGGGGAT GAC G DDX11 Ensembl:ENSG00000013573 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:31103843..31103944 32194978 MeRIP-seq:(Medium) rs753813009 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_418128,Human_RBP_ID_1470515,Human_RBP_ID_18160170,Human_RBP_ID_22039194,Human_RBP_ID_22173314,Human_RBP_ID_22793940,Human_RBP_ID_22903259,Human_RBP_ID_23208019,Human_RBP_ID_27213752 Human_Splice_Rec_1351938,Human_Splice_Rec_1351990,Human_Splice_Rec_1352116,Human_Splice_Rec_1352166,Human_Splice_Rec_1352230,Human_Splice_Rec_1352280,Human_Splice_Rec_1352340,Human_Splice_Rec_1352424,Human_Splice_Rec_1352434 Human_miRNA_ID_286571,Human_miRNA_ID_524602,Human_miRNA_ID_1539466,Human_miRNA_ID_1593490,Human_miRNA_ID_2060132,Human_miRNA_ID_2185528 RMVar_hsa_circ_118013,RMVar_hsa_circ_155643,RMVar_hsa_circ_97668,RMVar_hsa_circ_155647 101342 RMVar_ID_101342 Human_SNP_ID_495685825 m1A Human chr12 + 31103893 31103893 31103893 GCCGTGCCCTTCCTTTGTCCTGCCCGCTGGAGACAGTGTTTGTCGTGGGCGTGGTCTGCGGGGAT GCCGTGCCCTTCCTTTGTCCTGCCCGCTGGAGGCAGTGTTTGTCGTGGGCGTGGTCTGCGGGGAT A G DDX11 Ensembl:ENSG00000013573 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:31103843..31103944 32194978 MeRIP-seq:(Medium) rs1281430812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418128,Human_RBP_ID_1470515,Human_RBP_ID_18160170,Human_RBP_ID_22039194,Human_RBP_ID_22173314,Human_RBP_ID_22793940,Human_RBP_ID_22903259,Human_RBP_ID_23208019,Human_RBP_ID_27213752 Human_Splice_Rec_1351938,Human_Splice_Rec_1351990,Human_Splice_Rec_1352116,Human_Splice_Rec_1352166,Human_Splice_Rec_1352230,Human_Splice_Rec_1352280,Human_Splice_Rec_1352340,Human_Splice_Rec_1352424,Human_Splice_Rec_1352434 Human_miRNA_ID_286571,Human_miRNA_ID_524602,Human_miRNA_ID_1539466,Human_miRNA_ID_1593490,Human_miRNA_ID_2060132,Human_miRNA_ID_2185528 RMVar_hsa_circ_118013,RMVar_hsa_circ_155643,RMVar_hsa_circ_97668,RMVar_hsa_circ_155647 101343 RMVar_ID_101343 Human_SNP_ID_495732396 m1A Human chr12 - 31282510 31282510 31282510 TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGTTTATAGGTGCCCGCCACCAGACCCG TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGTTTATAGGTGCCCGCCACCAGACCCG T C SINHCAF Ensembl:ENSG00000139146 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs547472707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418248,Human_RBP_ID_23556169 101344 RMVar_ID_101344 Human_SNP_ID_495732424 m1A Human chr12 - 31282615 31282615 31282615 TACAAACTGACCCTCTTTTTTTTTTGAGACGGAGTTTTGCTCTTGTTACCCAGGCTGGAGTGCAG TACAAACTGACCCTCTTTTTTTTTTGAGACGGGGTTTTGCTCTTGTTACCCAGGCTGGAGTGCAG T C SINHCAF Ensembl:ENSG00000139146 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:31282432..31282633 32194978 MeRIP-seq:(Medium) rs1261064627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418250,Human_RBP_ID_6174785,Human_RBP_ID_17817247 Human_miRNA_ID_238522,Human_miRNA_ID_1730080 101345 RMVar_ID_101345 Human_SNP_ID_495742693 m1A Human chr12 - 31324017 31324017 31324017 TGTCTTATTTACCAACAAATCCACCAGGGAGCATTCTTACTTGCTGGCTCGGCGTCTCTCTCGGC TGTCTTATTTACCAACAAATCCACCAGGGAGCGTTCTTACTTGCTGGCTCGGCGTCTCTCTCGGC T C SINHCAF Ensembl:ENSG00000139146 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:31324015..31324116 32194978 MeRIP-seq:(Medium) rs1254996948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418260 Human_Splice_Rec_1352611 101346 RMVar_ID_101346 Human_SNP_ID_495743386 m1A Human chr12 + 31326081 31326081 31326081 CAATAATGTCCCCGAGGTGCGGAGTGCACGCCAGGCCAGTCCCCCTCAAGCGCTCCCTCCTCCTC CAATAATGTCCCCGAGGTGCGGAGTGCACGCCCGGCCAGTCCCCCTCAAGCGCTCCCTCCTCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:31325478..31326170;chr12:31326001..31326130 26863196 MeRIP-seq:(Medium) rs1299513495 Functional Loss SNV dbSNP153 33..33 33 - - - 101347 RMVar_ID_101347 Human_SNP_ID_495771270 m1A Human chr12 + 31435168 31435168 31435168 CCTATTCCCGTACCCACACAGACTAGTTCCCAATTTCTCTCACGACTACCCATGAATCACTTCAC CCTATTCCCGTACCCACACAGACTAGTTCCCAGTTTCTCTCACGACTACCCATGAATCACTTCAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:31435147..31435276 26863196 MeRIP-seq:(Medium) rs935189604 Functional Loss SNV dbSNP153 33..33 33 - - - 101348 RMVar_ID_101348 Human_SNP_ID_495810719 m1A Human chr12 + 31590850 31590850 31590850 GCAGCTCCCGCTCATCCCGGCCGCGCTGCTCCAGGGGCCGCCGCCGCCGCCGCCCGGGAAGGCTT GCAGCTCCCGCTCATCCCGGCCGCGCTGCTCCTGGGGCCGCCGCCGCCGCCGCCCGGGAAGGCTT A T DENND5B-AS1 Ensembl:ENSG00000255867 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31590799..31591129 26863196 MeRIP-seq:(Medium) rs1429067920 Functional Loss SNV dbSNP153 33..33 33 - - - 101349 RMVar_ID_101349 Human_SNP_ID_495810748 m1A Human chr12 - 31590954 31590929 31590954 AGGCTGCGGCGGCGAGAGGCGGCTGCGCGGCCATGGGCGCGCCAGTGTCGCCCTAGGGCGGGCGC AGGCTGCGGCGGCGAGAGGCGGCTGCGCGGCC_________________________GCGGGCGC CCCTAGGGCGACACTGGCGCGCCCAT C DENND5B Ensembl:ENSG00000170456 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:31590747..31591114;chr12:31590772..31590975 26863196 MeRIP-seq:(Medium) rs1399528333 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_4219525,Human_RBP_ID_18417426 101350 RMVar_ID_101350 Human_SNP_ID_495810754 m1A Human chr12 - 31590954 31590954 31590954 AGGCTGCGGCGGCGAGAGGCGGCTGCGCGGCCATGGGCGCGCCAGTGTCGCCCTAGGGCGGGCGC AGGCTGCGGCGGCGAGAGGCGGCTGCGCGGCCTTGGGCGCGCCAGTGTCGCCCTAGGGCGGGCGC T A DENND5B Ensembl:ENSG00000170456 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr12:31590747..31591114;chr12:31590772..31590975 26863196 MeRIP-seq:(Medium) rs1274427062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4219525,Human_RBP_ID_18417426 101351 RMVar_ID_101351 Human_SNP_ID_495816191 m1A Human chr12 + 31612995 31612991 31612995 AAGAGGGAAAGAAAGAAAAAGAAAGAAAGGAAAGAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGG AAGAGGGAAAGAAAGAAAAAGAAAGAAAG____GAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGG GGAAA G DENND5B-AS1 Ensembl:ENSG00000255867 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:31612950..31613054 26863196 MeRIP-seq:(Medium) rs147334005 Functional Loss DEL dbSNP153 30..33 33 - - - 101352 RMVar_ID_101352 Human_SNP_ID_495816192 m1A Human chr12 + 31612995 31612995 31612995 AAGAGGGAAAGAAAGAAAAAGAAAGAAAGGAAAGAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGG AAGAGGGAAAGAAAGAAAAAGAAAGAAAGGAAGGAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGG A G DENND5B-AS1 Ensembl:ENSG00000255867 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:31612950..31613054 26863196 MeRIP-seq:(Medium) rs1313067610 Functional Loss SNV dbSNP153 33..33 33 - - - 101353 RMVar_ID_101353 Human_SNP_ID_495816199 m1A Human chr12 + 31613005 31613002 31613006 GAAAGAAAAAGAAAGAAAGGAAAGAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGGAAAGACGGAA GAAAGAAAAAGAAAGAAAGGAAAGAAAGAG____AGAAAAGAAAAGAAAAGAAGGAAAGACGGAA GAGAA G DENND5B-AS1 Ensembl:ENSG00000255867 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31612925..31613083 26863196 MeRIP-seq:(Medium) rs200290301 Functional Loss DEL dbSNP153 31..34 33 - - - 101354 RMVar_ID_101354 Human_SNP_ID_495850326 m1A Human chr12 + 31754789 31754789 31754789 ACAGCGGCCAGCCCCCCAACTATGAGATGCTCAAGGAGGAGCACAAGGTGGCTGTGCTGGGGGTG ACAGCGGCCAGCCCCCCAACTATGAGATGCTCGAGGAGGAGCACAAGGTGGCTGTGCTGGGGGTG A G IFITM3P2 Ensembl:ENSG00000223722 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31754740..31754808 26863196 MeRIP-seq:(Medium) rs906205597 Functional Loss SNV dbSNP153 33..33 33 - - - 101355 RMVar_ID_101355 Human_SNP_ID_495944490 m1A Human chr12 + 32106869 32106869 32106869 CCGAGACTGCATCATTCCGCACCGGCTGCTGCAGGGCCAGAGGGAGCAGGTGGAGCGAGAGAGCG CCGAGACTGCATCATTCCGCACCGGCTGCTGCCGGGCCAGAGGGAGCAGGTGGAGCGAGAGAGCG A C BICD1 Ensembl:ENSG00000151746 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:32106820..32107427 26863196 MeRIP-seq:(Medium) rs1347914979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872959,Human_RBP_ID_4219618,Human_RBP_ID_5521421,Human_RBP_ID_6175528,Human_RBP_ID_18417251 101356 RMVar_ID_101356 Human_SNP_ID_495944518 m1A Human chr12 + 32106923 32106923 32106923 GCGAGAGAGCGAGCCGCGAGCCGGAGCGCGCCAGACCCAGGGCGAGACTGCAGTGACGCGGCCCG GCGAGAGAGCGAGCCGCGAGCCGGAGCGCGCCGGACCCAGGGCGAGACTGCAGTGACGCGGCCCG A G BICD1 Ensembl:ENSG00000151746 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:32106806..32107020 26863196 MeRIP-seq:(Medium) rs999665282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4219623,Human_RBP_ID_5521421,Human_RBP_ID_18417251 101357 RMVar_ID_101357 Human_SNP_ID_495949492 m1A Human chr12 + 32124763 32124761 32124763 GATGAAACAGCCTGTAGAAGAGGGAAGGCTGGAGAGAGTGCTGCTTGTCAGTGTCTGTGTTGTTG GATGAAACAGCCTGTAGAAGAGGGAAGGCTG__GAGAGTGCTGCTTGTCAGTGTCTGTGTTGTTG GGA G BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:32124713..32124867 26863196 MeRIP-seq:(Medium) rs1327145548 Functional Loss DEL dbSNP153 32..33 33 - - - 101358 RMVar_ID_101358 Human_SNP_ID_495997675 m1A Human chr12 + 32327569 32327569 32327569 TGACGGAGCAGCATGAGCGGGTGCACCGGCTCACAGAGCACGTCAATGCCATGAGGGGCCTGCAA TGACGGAGCAGCATGAGCGGGTGCACCGGCTCTCAGAGCACGTCAATGCCATGAGGGGCCTGCAA A T BICD1 Ensembl:ENSG00000151746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:32327519..32327703 26863196 MeRIP-seq:(Medium) rs1391832130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4219655,Human_RBP_ID_5521422 RMVar_hsa_circ_100488,RMVar_hsa_circ_155741,RMVar_hsa_circ_64326,RMVar_hsa_circ_155747,RMVar_hsa_circ_107515,RMVar_hsa_circ_155745,RMVar_hsa_circ_10695,RMVar_hsa_circ_294735,RMVar_hsa_circ_313748,RMVar_hsa_circ_285566,RMVar_hsa_circ_155748,RMVar_hsa_circ_155746 101359 RMVar_ID_101359 Human_SNP_ID_495997689 m1A Human chr12 - 32327622 32327622 32327622 CCTGAGTCCCGGCCCTTCTCCCCGTCCAGCTCAGCCTTGAGCTCCTTGCTGCTTTGCAGGCCCCT CCTGAGTCCCGGCCCTTCTCCCCGTCCAGCTCGGCCTTGAGCTCCTTGCTGCTTTGCAGGCCCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:32327528..32327679 26863196 MeRIP-seq:(Medium) rs768297946 Functional Loss SNV dbSNP153 33..33 33 - - - 101360 RMVar_ID_101360 Human_SNP_ID_496038711 m1A Human chr12 - 32494735 32494735 32494735 CAGTTCTTGCATCCTGGGCCCTCTTGGGTGCCAACCATGCCCTCTTTCTTGACCTTTCCTCCCTG CAGTTCTTGCATCCTGGGCCCTCTTGGGTGCCCACCATGCCCTCTTTCTTGACCTTTCCTCCCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:32494686..32494808 26863196 MeRIP-seq:(Medium) rs961637275 Functional Loss SNV dbSNP153 33..33 33 - - - 101361 RMVar_ID_101361 Human_SNP_ID_496084359 m1A Human chr12 - 32679354 32679354 32679354 ATGACAGGAATTAGCGCCTCCATGACTCTGAAAACACGGGGCCCCAGTGCCCGCCGGCCACGGCA ATGACAGGAATTAGCGCCTCCATGACTCTGAAGACACGGGGCCCCAGTGCCCGCCGGCCACGGCA T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:32679292..32679380 26863410 MeRIP-seq:(Medium) rs767578893 Functional Loss SNV dbSNP153 33..33 33 - - - 101362 RMVar_ID_101362 Human_SNP_ID_496084360 m1A Human chr12 - 32679354 32679354 32679354 ATGACAGGAATTAGCGCCTCCATGACTCTGAAAACACGGGGCCCCAGTGCCCGCCGGCCACGGCA ATGACAGGAATTAGCGCCTCCATGACTCTGAACACACGGGGCCCCAGTGCCCGCCGGCCACGGCA T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:32679292..32679380 26863410 MeRIP-seq:(Medium) rs767578893 Functional Loss SNV dbSNP153 33..33 33 - - - 101363 RMVar_ID_101363 Human_SNP_ID_496096315 m1A Human chr12 - 32726580 32726580 32726580 ATGATGCTGAAGCTATCCTTGCTGCAGACTTCAAAATTGGTCACTTTTTACGTGAGCATACAATC ATGATGCTGAAGCTATCCTTGCTGCAGACTTCGAAATTGGTCACTTTTTACGTGAGCATACAATC T C AC084824.2 Ensembl:ENSG00000257511 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs893151551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23556771,Human_RBP_ID_26415301,Human_RBP_ID_26905773 101364 RMVar_ID_101364 Human_SNP_ID_496102428 m1A Human chr12 + 32750727 32750727 32750727 GTGTTAATCATACTAAACTACTACCTTTTAGCAGAATCCAATCCTTCTCGTCCATGAACAAGCTT GTGTTAATCATACTAAACTACTACCTTTTAGCGGAATCCAATCCTTCTCGTCCATGAACAAGCTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:32750724..32753963 32194978 MeRIP-seq:(Medium) rs932680333 Functional Loss SNV dbSNP153 33..33 33 - - - 101365 RMVar_ID_101365 Human_SNP_ID_496137851 m1A Human chr12 + 32896637 32896637 32896637 TCCCCGCCAGCTTCAGCTTGGCCTCGGAGGGCAGCGCCAGGCTGGAGCTGTCCAGTTGTCCCAGG TCCCCGCCAGCTTCAGCTTGGCCTCGGAGGGCCGCGCCAGGCTGGAGCTGTCCAGTTGTCCCAGG A C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:32896591..32896753 26863196 MeRIP-seq:(Medium) rs1011184194 Functional Loss SNV dbSNP153 33..33 33 - - - 101366 RMVar_ID_101366 Human_SNP_ID_496474291 m1A Human chr12 - 34219738 34219738 34219738 CGTTCCCCTTGTGTTGTTGCCCATGTGTTGCTACCATGGTAATCCTGCTCAGTACGAGAGGAACC CGTTCCCCTTGTGTTGTTGCCCATGTGTTGCTGCCATGGTAATCCTGCTCAGTACGAGAGGAACC T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs61931964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269460,Human_RBP_ID_1082934,Human_RBP_ID_2367842,Human_RBP_ID_5274109,Human_RBP_ID_9016206,Human_RBP_ID_11928160,Human_RBP_ID_17062470,Human_RBP_ID_17067195,Human_RBP_ID_17186037,Human_RBP_ID_17470682,Human_RBP_ID_17684276,Human_RBP_ID_19760800,Human_RBP_ID_23556980,Human_RBP_ID_24407009,Human_RBP_ID_24466003,Human_RBP_ID_26415359 101367 RMVar_ID_101367 Human_SNP_ID_497950212 m1A Human chr12 + 38823194 38823194 38823194 GTAAGTCTCTGCCTCAAGTCCCCTCAAACACTATTCTTCTATTTTAGTCTTCTTCCTTATTCTGA GTAAGTCTCTGCCTCAAGTCCCCTCAAACACTGTTCTTCTATTTTAGTCTTCTTCCTTATTCTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:38823191..38823314 26863196 MeRIP-seq:(Medium) rs777275506 Functional Loss SNV dbSNP153 33..33 33 - - - 101368 RMVar_ID_101368 Human_SNP_ID_497969304 m1A Human chr12 + 38905573 38905573 38905573 AGGAGGCGCCTTGGACTTGTCCGGCGCCCACAACCACAGCTCGGGCGGACTGAGGGCTAGCTCCC AGGAGGCGCCTTGGACTTGTCCGGCGCCCACAGCCACAGCTCGGGCGGACTGAGGGCTAGCTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:38905522..38905603 26863196 MeRIP-seq:(Medium) rs368022308 Functional Loss SNV dbSNP153 33..33 33 - - - 101369 RMVar_ID_101369 Human_SNP_ID_497969642 m1A Human chr12 + 38906665 38906665 38906665 AACTGCATTCCAGGGCAGCAAGACTGGTGCCAAGACGGAGTCGTGGCAAAAGCATCCGGAGGTAG AACTGCATTCCAGGGCAGCAAGACTGGTGCCATGACGGAGTCGTGGCAAAAGCATCCGGAGGTAG A T CPNE8-AS1 Ensembl:ENSG00000257718 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:38906614..38906684 26863196 MeRIP-seq:(Medium) rs943923558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1354259 101370 RMVar_ID_101370 Human_SNP_ID_498103791 m1A Human chr12 - 39443019 39443019 39443019 GCGCCCGAGTCCCGCGGCCCCAGTGGCGCCTCAGCTCTGCGGTGCCGAGGCCCAACGGCTCGATC GCGCCCGAGTCCCGCGGCCCCAGTGGCGCCTCGGCTCTGCGGTGCCGAGGCCCAACGGCTCGATC T C KIF21A Ensembl:ENSG00000139116 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:39442975..39443046 26863196 MeRIP-seq:(Medium) rs572694199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4247372,Human_RBP_ID_9279544 Human_Splice_Rec_1354297,Human_Splice_Rec_1354369,Human_Splice_Rec_1354509,Human_Splice_Rec_1354575,Human_Splice_Rec_1354649 101371 RMVar_ID_101371 Human_SNP_ID_22517078 m1A Human chr1 + 90027445 90027443 90027446 GGAGGATGAAGAGAAGATTGATGAACCTATTGAAGAAGAGGAGGATGAAGATGAGGAAGAAGAAG GGAGGATGAAGAGAAGATTGATGAACCTATT___GAAGAGGAGGATGAAGATGAGGAAGAAGAAG TGAA T ZNF326 Ensembl:ENSG00000162664 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:90027351..90027758 26863196 MeRIP-seq:(Medium) rs776789754 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_25507,Human_RBP_ID_224439,Human_RBP_ID_1156362,Human_RBP_ID_4069061,Human_RBP_ID_5879142,Human_RBP_ID_8976883,Human_RBP_ID_9342858,Human_RBP_ID_17066775,Human_RBP_ID_18523437,Human_RBP_ID_22870881,Human_RBP_ID_24541170,Human_RBP_ID_26311495,Human_RBP_ID_27800511 Human_Splice_Rec_94640,Human_Splice_Rec_94658,Human_Splice_Rec_94686 101372 RMVar_ID_101372 Human_SNP_ID_22517114 m1A Human chr1 + 90027517 90027517 90027517 AGTGGGGGAAGTAGAGGAAGTGGAAGAAGTAGAGGAAGTGAGAGAAGGAGGAATAGAGGGCGAGG AGTGGGGGAAGTAGAGGAAGTGGAAGAAGTAGCGGAAGTGAGAGAAGGAGGAATAGAGGGCGAGG A C ZNF326 Ensembl:ENSG00000162664 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:90027351..90027761;chr1:90027351..90027725 26863196 MeRIP-seq:(Medium) rs1417188593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25507,Human_RBP_ID_190411,Human_RBP_ID_5879142,Human_RBP_ID_9547596,Human_RBP_ID_17066775,Human_RBP_ID_22869489,Human_RBP_ID_24541170,Human_RBP_ID_24736984 101373 RMVar_ID_101373 Human_SNP_ID_22717676 m1A Human chr1 + 90891921 90891921 90891921 TCCTCACTTCTCAGACGGGGTGGCTGCCAGGCAGAGGGTCTCCTCACTTCTCAGACGGGGCGGCT TCCTCACTTCTCAGACGGGGTGGCTGCCAGGCGGAGGGTCTCCTCACTTCTCAGACGGGGCGGCT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:90891901..90892014 26863196 MeRIP-seq:(Medium) rs1484275129 Functional Loss SNV dbSNP153 33..33 33 - - - 101374 RMVar_ID_101374 Human_SNP_ID_22718391 m1A Human chr1 + 90893924 90893924 90893924 AGTCCAGTCCGGCCTCCACGTGTGACTCCTGCATCCTCCCCTCAACCCCGGGAGACCGCCGCGGC AGTCCAGTCCGGCCTCCACGTGTGACTCCTGCCTCCTCCCCTCAACCCCGGGAGACCGCCGCGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:90893873..90894036 26863196 MeRIP-seq:(Medium) rs547985268 Functional Loss SNV dbSNP153 33..33 33 - - - 101375 RMVar_ID_101375 Human_SNP_ID_22726093 m1A Human chr1 - 90927732 90927732 90927732 AAACTTATATTTTAAAAAGCCTTTCATGAGACAGAGAAAAGATGGGTCTTTATATTTCTTAGCTA AAACTTATATTTTAAAAAGCCTTTCATGAGACGGAGAAAAGATGGGTCTTTATATTTCTTAGCTA T C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:90927730..90927901 26863196 MeRIP-seq:(Medium) rs1282580596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134438,RMVar_hsa_circ_266910,RMVar_hsa_circ_134439,RMVar_hsa_circ_353169,RMVar_hsa_circ_134437,RMVar_hsa_circ_318117 101376 RMVar_ID_101376 Human_SNP_ID_22737528 m1A Human chr1 - 90974880 90974876 90974881 TGGATGTGGGGAGTGGCTAGTCTCAAGAGATTAGACGAGAGAGTAAGGCTGGGCTATTTTATTGA TGGATGTGGGGAGTGGCTAGTCTCAAGAGAT_____GAGAGAGTAAGGCTGGGCTATTTTATTGA CGTCTA C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:90974878..90974974 26863196 MeRIP-seq:(Medium) rs1463543350 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_5880332,Human_RBP_ID_11146727 RMVar_hsa_circ_266910,RMVar_hsa_circ_353169,RMVar_hsa_circ_134437,RMVar_hsa_circ_134444,RMVar_hsa_circ_134448,RMVar_hsa_circ_134447,RMVar_hsa_circ_281136,RMVar_hsa_circ_304610,RMVar_hsa_circ_294120 101377 RMVar_ID_101377 Human_SNP_ID_22749002 m1A Human chr1 + 91021392 91021392 91021392 GGGGAGGGGTGTAGACAGTTAATGCCAGAGCCAGCGTTTCTGGCCACAACCGAGCAGCCTCAACG GGGGAGGGGTGTAGACAGTTAATGCCAGAGCCGGCGTTTCTGGCCACAACCGAGCAGCCTCAACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:91021388..91021582 26863196 MeRIP-seq:(Medium) rs376528790 Functional Loss SNV dbSNP153 33..33 33 - - - 101378 RMVar_ID_101378 Human_SNP_ID_22749186 m1A Human chr1 - 91021779 91021779 91021779 TGCCGCACAGGCTAAGATGGCGGCGGCGGCCGAGGAGGCGGAGTTGGTGCTACACAAGGAGCCCG TGCCGCACAGGCTAAGATGGCGGCGGCGGCCGGGGAGGCGGAGTTGGTGCTACACAAGGAGCCCG T C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:91021694..91022136 26863196 MeRIP-seq:(Medium) rs1418430393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330362 Human_Splice_Rec_94879 101379 RMVar_ID_101379 Human_SNP_ID_22839170 m1A Human chr1 - 91387225 91387223 91387225 TTGTTCACCCACTAATAGGGAACGTGAGCTGGAGGTTCTATTTCATAGACAAGACTGATGAAATC TTGTTCACCCACTAATAGGGAACGTGAGCTGG__GTTCTATTTCATAGACAAGACTGATGAAATC CCT C HFM1 Ensembl:ENSG00000162669 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs74417444 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_269274,Human_RBP_ID_273235,Human_RBP_ID_365142,Human_RBP_ID_980473,Human_RBP_ID_1073804,Human_RBP_ID_1123600,Human_RBP_ID_1156406,Human_RBP_ID_1258088,Human_RBP_ID_1350113,Human_RBP_ID_1439660,Human_RBP_ID_1756644,Human_RBP_ID_2173211,Human_RBP_ID_3325687,Human_RBP_ID_4069435,Human_RBP_ID_5156224,Human_RBP_ID_5253918,Human_RBP_ID_5273110,Human_RBP_ID_5414375,Human_RBP_ID_5434630,Human_RBP_ID_5458145,Human_RBP_ID_5487026,Human_RBP_ID_5538116,Human_RBP_ID_5880989,Human_RBP_ID_8050779,Human_RBP_ID_8241027,Human_RBP_ID_8321670,Human_RBP_ID_8752973,Human_RBP_ID_8977098,Human_RBP_ID_9252531,Human_RBP_ID_9269411,Human_RBP_ID_9548556,Human_RBP_ID_11148549,Human_RBP_ID_16978490,Human_RBP_ID_17061957,Human_RBP_ID_17098775,Human_RBP_ID_17182235,Human_RBP_ID_17220549,Human_RBP_ID_17337653,Human_RBP_ID_17455718,Human_RBP_ID_17678764,Human_RBP_ID_17760662,Human_RBP_ID_18198027,Human_RBP_ID_18205414,Human_RBP_ID_18235197,Human_RBP_ID_18430965,Human_RBP_ID_18509340,Human_RBP_ID_18523443,Human_RBP_ID_18583011,Human_RBP_ID_19029990,Human_RBP_ID_19154861,Human_RBP_ID_21878549,Human_RBP_ID_21910252,Human_RBP_ID_21999034,Human_RBP_ID_22022319,Human_RBP_ID_22148228,Human_RBP_ID_22376053,Human_RBP_ID_22420392,Human_RBP_ID_22488951,Human_RBP_ID_22531356,Human_RBP_ID_22786496,Human_RBP_ID_22875908,Human_RBP_ID_23122982,Human_RBP_ID_23150802,Human_RBP_ID_23262939,Human_RBP_ID_23303764,Human_RBP_ID_23419976,Human_RBP_ID_24398141,Human_RBP_ID_24454713,Human_RBP_ID_24528551,Human_RBP_ID_24538428,Human_RBP_ID_24539584,Human_RBP_ID_24738010,Human_RBP_ID_26384219,Human_RBP_ID_26592139,Human_RBP_ID_26747011,Human_RBP_ID_26871537,Human_RBP_ID_27153479,Human_RBP_ID_27187594,Human_RBP_ID_27401696,Human_RBP_ID_27555823,Human_RBP_ID_27600535 RMVar_hsa_circ_351744,RMVar_hsa_circ_37286,RMVar_hsa_circ_17351,RMVar_hsa_circ_32563,RMVar_hsa_circ_45860 101380 RMVar_ID_101380 Human_SNP_ID_22839172 m1A Human chr1 - 91387225 91387224 91387225 TTGTTCACCCACTAATAGGGAACGTGAGCTGGAGGTTCTATTTCATAGACAAGACTGATGAAATC TTGTTCACCCACTAATAGGGAACGTGAGCTGG_GGTTCTATTTCATAGACAAGACTGATGAAATC CT C HFM1 Ensembl:ENSG00000162669 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs374510506 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_269274,Human_RBP_ID_273235,Human_RBP_ID_365142,Human_RBP_ID_980473,Human_RBP_ID_1073804,Human_RBP_ID_1123600,Human_RBP_ID_1156406,Human_RBP_ID_1258088,Human_RBP_ID_1350113,Human_RBP_ID_1439660,Human_RBP_ID_1756644,Human_RBP_ID_2173211,Human_RBP_ID_3325687,Human_RBP_ID_4069435,Human_RBP_ID_5156224,Human_RBP_ID_5253918,Human_RBP_ID_5273110,Human_RBP_ID_5414375,Human_RBP_ID_5434630,Human_RBP_ID_5458145,Human_RBP_ID_5487026,Human_RBP_ID_5538116,Human_RBP_ID_5880989,Human_RBP_ID_8050779,Human_RBP_ID_8241027,Human_RBP_ID_8321670,Human_RBP_ID_8752973,Human_RBP_ID_8977098,Human_RBP_ID_9252531,Human_RBP_ID_9269411,Human_RBP_ID_9548556,Human_RBP_ID_11148549,Human_RBP_ID_16978490,Human_RBP_ID_17061957,Human_RBP_ID_17098775,Human_RBP_ID_17182235,Human_RBP_ID_17220549,Human_RBP_ID_17337653,Human_RBP_ID_17455718,Human_RBP_ID_17678764,Human_RBP_ID_17760662,Human_RBP_ID_18198027,Human_RBP_ID_18205414,Human_RBP_ID_18235197,Human_RBP_ID_18430965,Human_RBP_ID_18509340,Human_RBP_ID_18523443,Human_RBP_ID_18583011,Human_RBP_ID_19029990,Human_RBP_ID_19154861,Human_RBP_ID_21878549,Human_RBP_ID_21910252,Human_RBP_ID_21999034,Human_RBP_ID_22022319,Human_RBP_ID_22148228,Human_RBP_ID_22376053,Human_RBP_ID_22420392,Human_RBP_ID_22488951,Human_RBP_ID_22531356,Human_RBP_ID_22786496,Human_RBP_ID_22875908,Human_RBP_ID_23122982,Human_RBP_ID_23150802,Human_RBP_ID_23262939,Human_RBP_ID_23303764,Human_RBP_ID_23419976,Human_RBP_ID_24398141,Human_RBP_ID_24454713,Human_RBP_ID_24528551,Human_RBP_ID_24538428,Human_RBP_ID_24539584,Human_RBP_ID_24738010,Human_RBP_ID_26384219,Human_RBP_ID_26592139,Human_RBP_ID_26747011,Human_RBP_ID_26871537,Human_RBP_ID_27153479,Human_RBP_ID_27187594,Human_RBP_ID_27401696,Human_RBP_ID_27555823,Human_RBP_ID_27600535 RMVar_hsa_circ_351744,RMVar_hsa_circ_37286,RMVar_hsa_circ_17351,RMVar_hsa_circ_32563,RMVar_hsa_circ_45860 101381 RMVar_ID_101381 Human_SNP_ID_22839175 m1A Human chr1 - 91387225 91387225 91387225 TTGTTCACCCACTAATAGGGAACGTGAGCTGGAGGTTCTATTTCATAGACAAGACTGATGAAATC TTGTTCACCCACTAATAGGGAACGTGAGCTGGGGGTTCTATTTCATAGACAAGACTGATGAAATC T C HFM1 Ensembl:ENSG00000162669 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79658904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269274,Human_RBP_ID_273235,Human_RBP_ID_365142,Human_RBP_ID_980473,Human_RBP_ID_1073804,Human_RBP_ID_1123600,Human_RBP_ID_1156406,Human_RBP_ID_1258088,Human_RBP_ID_1350113,Human_RBP_ID_1439660,Human_RBP_ID_1756644,Human_RBP_ID_2173211,Human_RBP_ID_3325687,Human_RBP_ID_4069435,Human_RBP_ID_5156224,Human_RBP_ID_5253918,Human_RBP_ID_5273110,Human_RBP_ID_5414375,Human_RBP_ID_5434630,Human_RBP_ID_5458145,Human_RBP_ID_5487026,Human_RBP_ID_5538116,Human_RBP_ID_5880989,Human_RBP_ID_8050779,Human_RBP_ID_8241027,Human_RBP_ID_8321670,Human_RBP_ID_8752973,Human_RBP_ID_8977098,Human_RBP_ID_9252531,Human_RBP_ID_9269411,Human_RBP_ID_9548556,Human_RBP_ID_11148549,Human_RBP_ID_16978490,Human_RBP_ID_17061957,Human_RBP_ID_17098775,Human_RBP_ID_17182235,Human_RBP_ID_17220549,Human_RBP_ID_17337653,Human_RBP_ID_17455718,Human_RBP_ID_17678764,Human_RBP_ID_17760662,Human_RBP_ID_18198027,Human_RBP_ID_18205414,Human_RBP_ID_18235197,Human_RBP_ID_18430965,Human_RBP_ID_18509340,Human_RBP_ID_18523443,Human_RBP_ID_18583011,Human_RBP_ID_19029990,Human_RBP_ID_19154861,Human_RBP_ID_21878549,Human_RBP_ID_21910252,Human_RBP_ID_21999034,Human_RBP_ID_22022319,Human_RBP_ID_22148228,Human_RBP_ID_22376053,Human_RBP_ID_22420392,Human_RBP_ID_22488951,Human_RBP_ID_22531356,Human_RBP_ID_22786496,Human_RBP_ID_22875908,Human_RBP_ID_23122982,Human_RBP_ID_23150802,Human_RBP_ID_23262939,Human_RBP_ID_23303764,Human_RBP_ID_23419976,Human_RBP_ID_24398141,Human_RBP_ID_24454713,Human_RBP_ID_24528551,Human_RBP_ID_24538428,Human_RBP_ID_24539584,Human_RBP_ID_24738010,Human_RBP_ID_26384219,Human_RBP_ID_26592139,Human_RBP_ID_26747011,Human_RBP_ID_26871537,Human_RBP_ID_27153479,Human_RBP_ID_27187594,Human_RBP_ID_27401696,Human_RBP_ID_27555823,Human_RBP_ID_27600535 RMVar_hsa_circ_351744,RMVar_hsa_circ_37286,RMVar_hsa_circ_17351,RMVar_hsa_circ_32563,RMVar_hsa_circ_45860 101382 RMVar_ID_101382 Human_SNP_ID_22931166 m1A Human chr1 + 91769428 91769426 91769428 CATTCTCCTCCTAAACCAACTTCTCTCTGGGCACACACGGGCCCTGTTAACCTTCCCCTTTGCCC CATTCTCCTCCTAAACCAACTTCTCTCTGGG__CACACGGGCCCTGTTAACCTTCCCCTTTGCCC GCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:91769401..91769498 26863196 MeRIP-seq:(Medium) rs1286973385 Functional Loss DEL dbSNP153 32..33 33 - - - 101383 RMVar_ID_101383 Human_SNP_ID_22939198 m1A Human chr1 - 91802985 91802985 91802985 TATAGAAGACATTTTGGTGGAGATAAGAATTAAGAGCATCTTGCAGTAATCAGGGAACGAGAGAC TATAGAAGACATTTTGGTGGAGATAAGAATTAGGAGCATCTTGCAGTAATCAGGGAACGAGAGAC T C TGFBR3 Ensembl:ENSG00000069702 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:91802860..91802989 26863196 MeRIP-seq:(Medium) rs1418932425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94859,RMVar_hsa_circ_134483 101384 RMVar_ID_101384 Human_SNP_ID_22939536 m1A Human chr1 - 91804441 91804441 91804441 ACAGGTTCATGAGCTGGCTGTGGCAGAGGGAAAGGGACAGGAAGGCTAGGGCCTGACCCAGAAGT ACAGGTTCATGAGCTGGCTGTGGCAGAGGGAAGGGGACAGGAAGGCTAGGGCCTGACCCAGAAGT T C TGFBR3 Ensembl:ENSG00000069702 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:91804390..91804479 26863196 MeRIP-seq:(Medium) rs1411713262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17103497 RMVar_hsa_circ_94859,RMVar_hsa_circ_134483 101385 RMVar_ID_101385 Human_SNP_ID_22958237 m1A Human chr1 + 91885977 91885977 91885977 CCGCCCAGCGCTCGGCGGCGGCGAGCTCCGGCAGCTGCTGCGCCGCGGCAAAACTACGCCATCCG CCGCCCAGCGCTCGGCGGCGGCGAGCTCCGGCGGCTGCTGCGCCGCGGCAAAACTACGCCATCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:91885928..91885999 26863196 MeRIP-seq:(Medium) rs1460908531 Functional Loss SNV dbSNP153 33..33 33 - - - 101386 RMVar_ID_101386 Human_SNP_ID_22958306 m1A Human chr1 + 91886118 91886118 91886118 CCGACTGCCCTCCTTCACTCGCTGGGAAGAGGAAAGTGCCGCTCGGCGTCCCCGAAACCCTCGAT CCGACTGCCCTCCTTCACTCGCTGGGAAGAGGCAAGTGCCGCTCGGCGTCCCCGAAACCCTCGAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:91886068..91886233 26863196 MeRIP-seq:(Medium) rs1052752409 Functional Loss SNV dbSNP153 33..33 33 - - - 101387 RMVar_ID_101387 Human_SNP_ID_22958307 m1A Human chr1 + 91886118 91886118 91886118 CCGACTGCCCTCCTTCACTCGCTGGGAAGAGGAAAGTGCCGCTCGGCGTCCCCGAAACCCTCGAT CCGACTGCCCTCCTTCACTCGCTGGGAAGAGGGAAGTGCCGCTCGGCGTCCCCGAAACCCTCGAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:91886068..91886233 26863196 MeRIP-seq:(Medium) rs1052752409 Functional Loss SNV dbSNP153 33..33 33 - - - 101388 RMVar_ID_101388 Human_SNP_ID_23005473 m1A Human chr1 - 92074590 92074590 92074590 ATTGATGAAGGGGATGAGGATGAAGGTGAAGAAGATGAAGATGATGATGAAGGGGAGGAAGGAGA ATTGATGAAGGGGATGAGGATGAAGGTGAAGAGGATGAAGATGATGATGAAGGGGAGGAAGGAGA T C SETSIP Ensembl:ENSG00000230667 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:92074540..92074653 26863196 MeRIP-seq:(Medium) rs1296261238 Functional Loss SNV dbSNP153 33..33 33 - - - 101389 RMVar_ID_101389 Human_SNP_ID_23058613 m1A Human chr1 + 92298027 92298027 92298027 GCCATTCTTATTTCTCCTAGTTTCGATGCTAAAATCTACAAATACAAAACACACTGTTAACTATC GCCATTCTTATTTCTCCTAGTTTCGATGCTAATATCTACAAATACAAAACACACTGTTAACTATC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:92297945..92298051;chr1:92297966..92298077 26863196 MeRIP-seq:(Medium) rs1490689219 Functional Loss SNV dbSNP153 33..33 33 - - - 101390 RMVar_ID_101390 Human_SNP_ID_23058843 m1A Human chr1 + 92298930 92298930 92298930 CCTGAACCTCTCCACAACTCCACTTACCGGCCAGAACCCTCGCCTCTCCCAGCCGCCGCCACCTC CCTGAACCTCTCCACAACTCCACTTACCGGCCGGAACCCTCGCCTCTCCCAGCCGCCGCCACCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:92297907..92299000 26863196 MeRIP-seq:(Medium) rs1484794839 Functional Loss SNV dbSNP153 33..33 33 - - - 101391 RMVar_ID_101391 Human_SNP_ID_23175504 m1A Human chr1 - 92785052 92785052 92785052 GGACCCCGGAGGAACCAGCTGGCCAGCTGGCAAGGGGCTGGCTGCAGTTCCGACAGCGGCGGTGC GGACCCCGGAGGAACCAGCTGGCCAGCTGGCAGGGGGCTGGCTGCAGTTCCGACAGCGGCGGTGC T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:92784814..92785098 26863196 MeRIP-seq:(Medium) rs867409670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4075739,Human_RBP_ID_17761102,Human_RBP_ID_18415585 RMVar_hsa_circ_116196,RMVar_hsa_circ_134548,RMVar_hsa_circ_81207,RMVar_hsa_circ_134577 101392 RMVar_ID_101392 Human_SNP_ID_23187300 m1A Human chr1 - 92832102 92832102 92832102 CCGAGGCATCCACTCACCATCCTGCGGAACAGAGACCGGCGTCCGCTGCTCGACAGAGACCTGCA CCGAGGCATCCACTCACCATCCTGCGGAACAGTGACCGGCGTCCGCTGCTCGACAGAGACCTGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:92832024..92832421;chr1:92832026..92832158;chr1:92832026..92832177;chr1:92832051..92832189 26863196 MeRIP-seq:(Medium) rs758757902 Functional Loss SNV dbSNP153 33..33 33 - - - 101393 RMVar_ID_101393 Human_SNP_ID_23187301 m1A Human chr1 - 92832102 92832102 92832102 CCGAGGCATCCACTCACCATCCTGCGGAACAGAGACCGGCGTCCGCTGCTCGACAGAGACCTGCA CCGAGGCATCCACTCACCATCCTGCGGAACAGCGACCGGCGTCCGCTGCTCGACAGAGACCTGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:92832024..92832421;chr1:92832026..92832158;chr1:92832026..92832177;chr1:92832051..92832189 26863196 MeRIP-seq:(Medium) rs758757902 Functional Loss SNV dbSNP153 33..33 33 - - - 101394 RMVar_ID_101394 Human_SNP_ID_23187303 m1A Human chr1 - 92832104 92832104 92832104 GACCGAGGCATCCACTCACCATCCTGCGGAACAGAGACCGGCGTCCGCTGCTCGACAGAGACCTG GACCGAGGCATCCACTCACCATCCTGCGGAACGGAGACCGGCGTCCGCTGCTCGACAGAGACCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:92832026..92832125 32194978 MeRIP-seq:(Medium) rs201525257 Functional Loss SNV dbSNP153 33..33 33 - - - 101395 RMVar_ID_101395 Human_SNP_ID_23187860 m1A Human chr1 - 92833559 92833559 92833559 ATCTTGTATCACCAAGCGTTTCCGAGCATAATAATCAGTTTTACCCTCTGAAAGAAAAAAATAAT ATCTTGTATCACCAAGCGTTTCCGAGCATAATGATCAGTTTTACCCTCTGAAAGAAAAAAATAAT T C DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:92833376..92833816 32194978 MeRIP-seq:(Medium) rs748318627 Functional Loss SNV dbSNP153 33..33 33 - - - 101396 RMVar_ID_101396 Human_SNP_ID_23188608 m1A Human chr1 + 92836292 92836292 92836292 TGGAAAGCATTGATGGTCAGCCAGGTGCCTTCACCTGCTATTTGGATGCAGGCCTTGCCAGAACT TGGAAAGCATTGATGGTCAGCCAGGTGCCTTCGCCTGCTATTTGGATGCAGGCCTTGCCAGAACT A G RPL5 Ensembl:ENSG00000122406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:92836242..92836323 26863196 MeRIP-seq:(Medium) rs767564815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_365533,Human_RBP_ID_980571,Human_RBP_ID_1258186,Human_RBP_ID_1437099,Human_RBP_ID_1757000,Human_RBP_ID_8322056,Human_RBP_ID_8977338,Human_RBP_ID_11156468,Human_RBP_ID_18583369,Human_RBP_ID_22025977,Human_RBP_ID_22749251,Human_RBP_ID_23420986,Human_RBP_ID_27600786 Human_miRNA_ID_2930669 RMVar_hsa_circ_51739,RMVar_hsa_circ_83856,RMVar_hsa_circ_104760,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_134578,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_82928,RMVar_hsa_circ_53523,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_286813,RMVar_hsa_circ_134582,RMVar_hsa_circ_268549,RMVar_hsa_circ_126564,RMVar_hsa_circ_134583,RMVar_hsa_circ_134584,RMVar_hsa_circ_339049,RMVar_hsa_circ_134585,RMVar_hsa_circ_134586,RMVar_hsa_circ_96767,RMVar_hsa_circ_134587 101397 RMVar_ID_101397 Human_SNP_ID_23245221 m1A Human chr1 + 93079349 93079349 93079349 TTGAAGTGGGCTGTGTTTGAGGCCGGTGTAAGAACGCTCATTCTACCCCCAACCCTTGTCTCCAA TTGAAGTGGGCTGTGTTTGAGGCCGGTGTAAGGACGCTCATTCTACCCCCAACCCTTGTCTCCAA A G MTF2 Ensembl:ENSG00000143033 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:93079301..93079458 26863196 MeRIP-seq:(Medium) rs895396199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1437167,Human_RBP_ID_1757048,Human_RBP_ID_4074185,Human_RBP_ID_5434662,Human_RBP_ID_5487072,Human_RBP_ID_11157229,Human_RBP_ID_18583444,Human_RBP_ID_22786562,Human_RBP_ID_23421125,Human_RBP_ID_27798274 101398 RMVar_ID_101398 Human_SNP_ID_23257948 m1A Human chr1 + 93131749 93131749 93131749 AACCTGTTTTTGTGTGTAAGTAGGAATGATCCAGTGGAGAAGAGGAAATTGGTATAGGAGAGTAG AACCTGTTTTTGTGTGTAAGTAGGAATGATCCGGTGGAGAAGAGGAAATTGGTATAGGAGAGTAG A G MTF2 Ensembl:ENSG00000143033 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93131702..93131785 26863196 MeRIP-seq:(Medium) rs1455292819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11158775,Human_RBP_ID_23421316 RMVar_hsa_circ_68849,RMVar_hsa_circ_134604,RMVar_hsa_circ_292912,RMVar_hsa_circ_13601,RMVar_hsa_circ_340119 101399 RMVar_ID_101399 Human_SNP_ID_23268973 m1A Human chr1 + 93180152 93180152 93180152 GGGAAGGGTAAAGGTGAAGTCGCTATCGAGGGAAGGTGTGAAGCCGGCCGCCCCAGGCAGCAGCA GGGAAGGGTAAAGGTGAAGTCGCTATCGAGGGGAGGTGTGAAGCCGGCCGCCCCAGGCAGCAGCA A G CCDC18 Ensembl:ENSG00000122483 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:93180101..93180578 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - RMVar_hsa_circ_134605,RMVar_hsa_circ_134607 101400 RMVar_ID_101400 Human_SNP_ID_23306459 m1A Human chr1 + 93346024 93346024 93346024 TGCGTTCGGGCTACGCGGCCACGGCGGCAGCCACTGCGACTCCCACTGTGCCTGGCTCTGTCCAT TGCGTTCGGGCTACGCGGCCACGGCGGCAGCCGCTGCGACTCCCACTGTGCCTGGCTCTGTCCAT A G DR1 Ensembl:ENSG00000117505 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:93345979..93346150 26863196 MeRIP-seq:(Medium) rs1062896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221552,Human_RBP_ID_742240,Human_RBP_ID_802898,Human_RBP_ID_858528,Human_RBP_ID_4070722,Human_RBP_ID_5458182,Human_RBP_ID_9319030,Human_RBP_ID_22023546,Human_RBP_ID_26872141 Human_miRNA_ID_1994245,Human_miRNA_ID_2226739,Human_miRNA_ID_2502715 RMVar_hsa_circ_100933,RMVar_hsa_circ_134633 101401 RMVar_ID_101401 Human_SNP_ID_23306558 m1A Human chr1 - 93346298 93346298 93346298 AGGGGCGGGCGCTGTCGCCTAACTGGTCCCCAACGGCGTCGGAGCAGAGGCAAGATCCAGGGGCA AGGGGCGGGCGCTGTCGCCTAACTGGTCCCCAGCGGCGTCGGAGCAGAGGCAAGATCCAGGGGCA T C CCDC18-AS1,CCDC18-AS1:2,CCDC18-AS1:3,CCDC18-AS1:4,CCDC18-AS1:5 RNACentral:URS0000D5E26B,RNACentral:URS0000D5B9E2,RNACentral:URS0000D59742,RNACentral:URS0000D5D352,RNACentral:URS0000D573C5 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:93346251..93346425 26863196 MeRIP-seq:(Medium) rs933928955 Functional Loss SNV dbSNP153 33..33 33 - - - 101402 RMVar_ID_101402 Human_SNP_ID_23330597 m1A Human chr1 - 93448154 93448154 93448154 AGCTCAGCGGGTCTACCTCGAAAGGTGCCGCCACCGCCGGGCTCCCCAGTGAGTGAGAAAGACGC AGCTCAGCGGGTCTACCTCGAAAGGTGCCGCCGCCGCCGGGCTCCCCAGTGAGTGAGAAAGACGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93448105..93448244 26863196 MeRIP-seq:(Medium) rs952479688 Functional Loss SNV dbSNP153 33..33 33 - - - 101403 RMVar_ID_101403 Human_SNP_ID_23381158 m1A Human chr1 + 93659691 93659691 93659691 AGATGACAATCACGGTTCTAAGGTCTTGCCCAACTCACCAGCCTAATCTCCTCACCTTGCTCCTT AGATGACAATCACGGTTCTAAGGTCTTGCCCAGCTCACCAGCCTAATCTCCTCACCTTGCTCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93659689..93659877 26863196 MeRIP-seq:(Medium) rs191007951 Functional Loss SNV dbSNP153 33..33 33 - - - 101404 RMVar_ID_101404 Human_SNP_ID_23382547 m1A Human chr1 - 93665798 93665798 93665798 GGCTTTATTTGTTTGGTTGATTGCATTTTCTTAGGGAAGGGGGTTATGGTAGATTGCTGAGAATC GGCTTTATTTGTTTGGTTGATTGCATTTTCTTGGGGAAGGGGGTTATGGTAGATTGCTGAGAATC T C BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93665793..93665876 26863196 MeRIP-seq:(Medium) rs984180543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42663,RMVar_hsa_circ_134657,RMVar_hsa_circ_293349 101405 RMVar_ID_101405 Human_SNP_ID_23384653 m1A Human chr1 - 93674922 93674922 93674922 CTTTCCCCCTTAGAGTTGAGAATTATGGCTGCAGGAAAATTTGCAAGCCTTCCCAGAAACATGCC CTTTCCCCCTTAGAGTTGAGAATTATGGCTGCGGGAAAATTTGCAAGCCTTCCCAGAAACATGCC T C BCAR3 Ensembl:ENSG00000137936 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93674873..93674993 26863196 MeRIP-seq:(Medium) rs920736982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20544 Human_Splice_Rec_97186,Human_Splice_Rec_97244,Human_Splice_Rec_97266 RMVar_hsa_circ_42663,RMVar_hsa_circ_134657,RMVar_hsa_circ_293349,RMVar_hsa_circ_311538,RMVar_hsa_circ_345163,RMVar_hsa_circ_134658 101406 RMVar_ID_101406 Human_SNP_ID_23384654 m1A Human chr1 - 93674922 93674922 93674922 CTTTCCCCCTTAGAGTTGAGAATTATGGCTGCAGGAAAATTTGCAAGCCTTCCCAGAAACATGCC CTTTCCCCCTTAGAGTTGAGAATTATGGCTGCCGGAAAATTTGCAAGCCTTCCCAGAAACATGCC T G BCAR3 Ensembl:ENSG00000137936 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93674873..93674993 26863196 MeRIP-seq:(Medium) rs920736982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20544 Human_Splice_Rec_97186,Human_Splice_Rec_97244,Human_Splice_Rec_97266 RMVar_hsa_circ_42663,RMVar_hsa_circ_134657,RMVar_hsa_circ_293349,RMVar_hsa_circ_311538,RMVar_hsa_circ_345163,RMVar_hsa_circ_134658 101407 RMVar_ID_101407 Human_SNP_ID_23407605 m1A Human chr1 + 93779976 93779976 93779976 GGCCTCCACCCAAAAGGTAAACCCCTCAGGACATGTCTTCTCATCCTCAAACCCACATTGTTTCC GGCCTCCACCCAAAAGGTAAACCCCTCAGGACCTGTCTTCTCATCCTCAAACCCACATTGTTTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93779925..93780116 26863196 MeRIP-seq:(Medium) rs927442019 Functional Loss SNV dbSNP153 33..33 33 - - - 101408 RMVar_ID_101408 Human_SNP_ID_23418223 m1A Human chr1 - 93831773 93831773 93831773 TAAGCCGGACAGGATGTGAGGAGGGGATGATAAAAGGATTATAGGGTGGGGAAGTGGAGGCTGAG TAAGCCGGACAGGATGTGAGGAGGGGATGATACAAGGATTATAGGGTGGGGAAGTGGAGGCTGAG T G BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93831723..93831819 26863196 MeRIP-seq:(Medium) rs1297039646 Functional Loss SNV dbSNP153 33..33 33 - - - 101409 RMVar_ID_101409 Human_SNP_ID_23418892 m1A Human chr1 - 93834584 93834584 93834584 CTAGGCTGAAAGAGTAAGGTCACGTTGTTTGGACAGAAAGGCTACAGAGCGCAGTCCTGGCTCTT CTAGGCTGAAAGAGTAAGGTCACGTTGTTTGGTCAGAAAGGCTACAGAGCGCAGTCCTGGCTCTT T A BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93834540..93834647 26863196 MeRIP-seq:(Medium) rs995485521 Functional Loss SNV dbSNP153 33..33 33 - - - 101410 RMVar_ID_101410 Human_SNP_ID_23418924 m1A Human chr1 - 93834747 93834747 93834747 GCCGAAGGAGCCAGAGGGCAGAAAGTATGTGCATCAGATGTGAGGAAGAAAATAGATTTTGGAAG GCCGAAGGAGCCAGAGGGCAGAAAGTATGTGCCTCAGATGTGAGGAAGAAAATAGATTTTGGAAG T G BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93834555..93834952 26863196 MeRIP-seq:(Medium) rs1027971317 Functional Loss SNV dbSNP153 33..33 33 - - - 101411 RMVar_ID_101411 Human_SNP_ID_23419565 m1A Human chr1 + 93837376 93837373 93837377 AGTTGCTCTGTGTTTTGTGTTTTCTGTGTTTCACTCACTTAGTTCAATGTAATTGATGCACCTTC AGTTGCTCTGTGTTTTGTGTTTTCTGTGTT____TCACTTAGTTCAATGTAATTGATGCACCTTC TTCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93837368..93837507 26863196 MeRIP-seq:(Medium) rs111963609 Functional Loss DEL dbSNP153 31..34 33 - - - 101412 RMVar_ID_101412 Human_SNP_ID_23420772 m1A Human chr1 - 93842769 93842769 93842769 ACAGTTTGGGGTGATGGAAGATGTGTCAACAGACGAGGTTGGGAAGGTAGGATCCAGGCCAGATA ACAGTTTGGGGTGATGGAAGATGTGTCAACAGGCGAGGTTGGGAAGGTAGGATCCAGGCCAGATA T C BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93842629..93842811 26863196 MeRIP-seq:(Medium) rs1311974313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11164570 101413 RMVar_ID_101413 Human_SNP_ID_23422403 m1A Human chr1 + 93847603 93847603 93847603 GTGGCTCCGTGGCGCAATGGATAGCGCATTGGACTTCTAGAGGCTGAAGGCATTCAAAGGTTCCG GTGGCTCCGTGGCGCAATGGATAGCGCATTGGCCTTCTAGAGGCTGAAGGCATTCAAAGGTTCCG A C AL049796.1 Ensembl:ENSG00000260464 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93847054..93847818 26863196 MeRIP-seq:(Medium) rs939324864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273272,Human_RBP_ID_366145,Human_RBP_ID_1063845,Human_RBP_ID_1123684,Human_RBP_ID_1156547,Human_RBP_ID_1258290,Human_RBP_ID_1350240,Human_RBP_ID_1437596,Human_RBP_ID_1757391,Human_RBP_ID_2176299,Human_RBP_ID_3326926,Human_RBP_ID_5091306,Human_RBP_ID_5156248,Human_RBP_ID_5253990,Human_RBP_ID_5280458,Human_RBP_ID_5434689,Human_RBP_ID_5458198,Human_RBP_ID_5487100,Human_RBP_ID_5538152,Human_RBP_ID_5642793,Human_RBP_ID_5886027,Human_RBP_ID_8241059,Human_RBP_ID_8322557,Human_RBP_ID_8753237,Human_RBP_ID_8977605,Human_RBP_ID_11164574,Human_RBP_ID_17337816,Human_RBP_ID_17678856,Human_RBP_ID_17761624,Human_RBP_ID_18205063,Human_RBP_ID_18235725,Human_RBP_ID_18431026,Human_RBP_ID_18584448,Human_RBP_ID_19435036,Human_RBP_ID_22786617,Human_RBP_ID_22871980,Human_RBP_ID_23110132,Human_RBP_ID_23117717,Human_RBP_ID_23123030,Human_RBP_ID_23422112,Human_RBP_ID_26384595,Human_RBP_ID_26592611,Human_RBP_ID_27153492,Human_RBP_ID_27187940,Human_RBP_ID_27401938,Human_RBP_ID_27601141 Human_miRNA_ID_3201311 101414 RMVar_ID_101414 Human_SNP_ID_23422404 m1A Human chr1 + 93847603 93847603 93847603 GTGGCTCCGTGGCGCAATGGATAGCGCATTGGACTTCTAGAGGCTGAAGGCATTCAAAGGTTCCG GTGGCTCCGTGGCGCAATGGATAGCGCATTGGGCTTCTAGAGGCTGAAGGCATTCAAAGGTTCCG A G AL049796.1 Ensembl:ENSG00000260464 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:93847054..93847818 26863196 MeRIP-seq:(Medium) rs939324864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273272,Human_RBP_ID_366145,Human_RBP_ID_1063845,Human_RBP_ID_1123684,Human_RBP_ID_1156547,Human_RBP_ID_1258290,Human_RBP_ID_1350240,Human_RBP_ID_1437596,Human_RBP_ID_1757391,Human_RBP_ID_2176299,Human_RBP_ID_3326926,Human_RBP_ID_5091306,Human_RBP_ID_5156248,Human_RBP_ID_5253990,Human_RBP_ID_5280458,Human_RBP_ID_5434689,Human_RBP_ID_5458198,Human_RBP_ID_5487100,Human_RBP_ID_5538152,Human_RBP_ID_5642793,Human_RBP_ID_5886027,Human_RBP_ID_8241059,Human_RBP_ID_8322557,Human_RBP_ID_8753237,Human_RBP_ID_8977605,Human_RBP_ID_11164574,Human_RBP_ID_17337816,Human_RBP_ID_17678856,Human_RBP_ID_17761624,Human_RBP_ID_18205063,Human_RBP_ID_18235725,Human_RBP_ID_18431026,Human_RBP_ID_18584448,Human_RBP_ID_19435036,Human_RBP_ID_22786617,Human_RBP_ID_22871980,Human_RBP_ID_23110132,Human_RBP_ID_23117717,Human_RBP_ID_23123030,Human_RBP_ID_23422112,Human_RBP_ID_26384595,Human_RBP_ID_26592611,Human_RBP_ID_27153492,Human_RBP_ID_27187940,Human_RBP_ID_27401938,Human_RBP_ID_27601141 Human_miRNA_ID_3201311 101415 RMVar_ID_101415 Human_SNP_ID_23422422 m1A Human chr1 - 93847631 93847631 93847631 GCGTTACGACTCCGCCGGGACTCGAACCCGGAACCTTTGAATGCCTTCAGCCTCTAGAAGTCCAA GCGTTACGACTCCGCCGGGACTCGAACCCGGACCCTTTGAATGCCTTCAGCCTCTAGAAGTCCAA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr1:93847479..93847718;chr1:93847095..93847811 26863196 MeRIP-seq:(Medium) rs570638631 Functional Loss SNV dbSNP153 33..33 33 - - - 101416 RMVar_ID_101416 Human_SNP_ID_23422426 m1A Human chr1 - 93847638 93847638 93847638 GAAAAAAGCGTTACGACTCCGCCGGGACTCGAACCCGGAACCTTTGAATGCCTTCAGCCTCTAGA GAAAAAAGCGTTACGACTCCGCCGGGACTCGAGCCCGGAACCTTTGAATGCCTTCAGCCTCTAGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:93847530..93847810 26863196 MeRIP-seq:(Medium) rs1557710113 Functional Loss SNV dbSNP153 33..33 33 - - - 101417 RMVar_ID_101417 Human_SNP_ID_23430859 m1A Human chr1 + 93879144 93879144 93879144 TGCTGGCCTTAGCCCGTGCAGATCTGGTAACCACCATCTTTCCGGCTCCCTCGCGACCACCACGA TGCTGGCCTTAGCCCGTGCAGATCTGGTAACCCCCATCTTTCCGGCTCCCTCGCGACCACCACGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93879043..93879200 26863196 MeRIP-seq:(Medium) rs1264657757 Functional Loss SNV dbSNP153 33..33 33 - - - 101418 RMVar_ID_101418 Human_SNP_ID_23437690 m1A Human chr1 - 93909283 93909283 93909283 CGCAGACCAGGCTCCAGCCGCGCGGCGCCGGCAGCCTCGCGCTCCCTCTCGGGTCTCTCTCGGGC CGCAGACCAGGCTCCAGCCGCGCGGCGCCGGCCGCCTCGCGCTCCCTCTCGGGTCTCTCTCGGGC T G GCLM Ensembl:ENSG00000023909 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:93909244..93909491 26863196 MeRIP-seq:(Medium) rs1235832658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223412,Human_RBP_ID_4074196,Human_RBP_ID_9270222,Human_RBP_ID_9319035,Human_RBP_ID_22427339 101419 RMVar_ID_101419 Human_SNP_ID_23517926 m1A Human chr1 - 94237462 94237462 94237462 GAGCTCCAGCCCTCGGCGGTGGCGGCGGCCGTAGGTGTGGGGCGGGCGTCCGCGTCCGGCACGCG GAGCTCCAGCCCTCGGCGGTGGCGGCGGCCGTCGGTGTGGGGCGGGCGTCCGCGTCCGGCACGCG T G ARHGAP29 Ensembl:ENSG00000137962 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:94237430..94237577;chr1:94237460..94237562 26863196 MeRIP-seq:(Medium) rs960021647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4071145,Human_RBP_ID_17100972 Human_Splice_Rec_97663,Human_Splice_Rec_97725 101420 RMVar_ID_101420 Human_SNP_ID_23517971 m1A Human chr1 + 94237567 94237567 94237567 TCTCAGCCGCAGCCGCAGCCGCAGCCACAGCCACAGGCACCACCACCACTGCAGCCGCCACCGCC TCTCAGCCGCAGCCGCAGCCGCAGCCACAGCCGCAGGCACCACCACCACTGCAGCCGCCACCGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:94237421..94237600 26863196 MeRIP-seq:(Medium) rs1410705727 Functional Loss SNV dbSNP153 33..33 33 - - - 101421 RMVar_ID_101421 Human_SNP_ID_23520374 m1A Human chr1 + 94247701 94247701 94247701 CAGACGCCCGGCCAAGTGGCAGCCGCAGCCACAGACACCACCACCACCACCACCACAGCGGCCGC CAGACGCCCGGCCAAGTGGCAGCCGCAGCCACTGACACCACCACCACCACCACCACAGCGGCCGC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:94247454..94247731 26863196 MeRIP-seq:(Medium) rs1303066283 Functional Loss SNV dbSNP153 33..33 33 - - - 101422 RMVar_ID_101422 Human_SNP_ID_23559626 m1A Human chr1 + 94418473 94418473 94418473 CCGCGTCCCCTCGCCGGCTCGCTGGTACCGGCAGTGCCATGGCGGCCTTCAGCAAGTACTTGACG CCGCGTCCCCTCGCCGGCTCGCTGGTACCGGCTGTGCCATGGCGGCCTTCAGCAAGTACTTGACG A T ABCD3 Ensembl:ENSG00000117528 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:94418423..94418758;chr1:94418391..94418666;chr1:94418424..94418624 26863196 MeRIP-seq:(Medium) rs1414331459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4071157,Human_RBP_ID_18415009 Human_miRNA_ID_2133328 RMVar_hsa_circ_107372,RMVar_hsa_circ_134678 101423 RMVar_ID_101423 Human_SNP_ID_23574340 m1A Human chr1 + 94479925 94479925 94479925 TAGTACAGCAGCTGGAAGCAAGATGTACACGCAGGGAAAGACAGAGCTCGTTCAGGGGGAGCTGA TAGTACAGCAGCTGGAAGCAAGATGTACACGCTGGGAAAGACAGAGCTCGTTCAGGGGGAGCTGA A T ABCD3 Ensembl:ENSG00000117528 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:94479909..94480254 26863196 MeRIP-seq:(Medium) rs767500666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107372,RMVar_hsa_circ_134678,RMVar_hsa_circ_134687,RMVar_hsa_circ_134679,RMVar_hsa_circ_134681,RMVar_hsa_circ_134680,RMVar_hsa_circ_284222,RMVar_hsa_circ_322939,RMVar_hsa_circ_347732,RMVar_hsa_circ_312200,RMVar_hsa_circ_279761,RMVar_hsa_circ_280841,RMVar_hsa_circ_134688,RMVar_hsa_circ_134690,RMVar_hsa_circ_326264,RMVar_hsa_circ_352436,RMVar_hsa_circ_345152,RMVar_hsa_circ_66105,RMVar_hsa_circ_325875,RMVar_hsa_circ_134691,RMVar_hsa_circ_134693,RMVar_hsa_circ_331620,RMVar_hsa_circ_377653,RMVar_hsa_circ_134692,RMVar_hsa_circ_310763,RMVar_hsa_circ_45473,RMVar_hsa_circ_73747,RMVar_hsa_circ_134695,RMVar_hsa_circ_134696,RMVar_hsa_circ_365212,RMVar_hsa_circ_67137 101424 RMVar_ID_101424 Human_SNP_ID_23589142 m1A Human chr1 - 94541632 94541623 94541632 CGCTCGATCTCGCCGCCAACTGGTAGACATGGAGACCCCTGCCTGGCCCCGGGTCCCGCGCCCCG CGCTCGATCTCGCCGCCAACTGGTAGACATGG_________CCTGGCCCCGGGTCCCGCGCCCCG GCAGGGGTCT G F3 Ensembl:ENSG00000117525 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:94541581..94541799;chr1:94541592..94541763 26863196 MeRIP-seq:(Medium) rs1437305306 Functional Loss DEL dbSNP153 33..41 33 - - - Human_Splice_Rec_97983,Human_Splice_Rec_97993,Human_Splice_Rec_98003 Human_miRNA_ID_2660868,Human_miRNA_ID_2679321 RMVar_hsa_circ_90278,RMVar_hsa_circ_134711 101425 RMVar_ID_101425 Human_SNP_ID_23675730 m1A Human chr1 + 94903504 94903504 94903504 TCTATCCAATTGCGAAGATCTTCTTCTGCCTGATGATCATACTTGGAAGCAATCTGAAATACAGG TCTATCCAATTGCGAAGATCTTCTTCTGCCTGTTGATCATACTTGGAAGCAATCTGAAATACAGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:94903401..94924218 32194978 MeRIP-seq:(Medium) rs771780236 Functional Loss SNV dbSNP153 33..33 33 - - - 101426 RMVar_ID_101426 Human_SNP_ID_23681191 m1A Human chr1 + 94926974 94926974 94926974 CGCACTTCGCTTCCCCGCTCCTGGCCCCGAGGAGTGGCCGCCGCGGGGGATGCTCGAACTCCCTC CGCACTTCGCTTCCCCGCTCCTGGCCCCGAGGTGTGGCCGCCGCGGGGGATGCTCGAACTCCCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr1:94926933..94927053;chr1:94926826..94927125 26863196,32194978 MeRIP-seq:(Medium) rs1001888883 Functional Loss SNV dbSNP153 33..33 33 - - - 101427 RMVar_ID_101427 Human_SNP_ID_23681208 m1A Human chr1 + 94927025 94927025 94927025 GCTCGAACTCCCTCCTCTGGGAGGCGCAGGAGACGGCCGCGGGGCGCGGGCGGTGCCTGGGCGAC GCTCGAACTCCCTCCTCTGGGAGGCGCAGGAGGCGGCCGCGGGGCGCGGGCGGTGCCTGGGCGAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:94926942..94927070;chr1:94926876..94927125 26863410 MeRIP-seq:(Medium) rs988289004 Functional Loss SNV dbSNP153 33..33 33 - - - 101428 RMVar_ID_101428 Human_SNP_ID_23714468 m1A Human chr1 + 95072852 95072852 95072852 GAAGCACTACCCATATTCGCAGGATTAGGAAAACCGCCACAGCTCCTGCGGCCGCAGCTAGAACG GAAGCACTACCCATATTCGCAGGATTAGGAAACCCGCCACAGCTCCTGCGGCCGCAGCTAGAACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:95072802..95072895 26863196 MeRIP-seq:(Medium) rs773486977 Functional Loss SNV dbSNP153 33..33 33 - - - 101429 RMVar_ID_101429 Human_SNP_ID_23714472 m1A Human chr1 + 95072860 95072856 95072860 ACCCATATTCGCAGGATTAGGAAAACCGCCACAGCTCCTGCGGCCGCAGCTAGAACGAGAACGCA ACCCATATTCGCAGGATTAGGAAAACCGC____GCTCCTGCGGCCGCAGCTAGAACGAGAACGCA CCACA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:95072813..95072912 26863196 MeRIP-seq:(Medium) rs1274864679 Functional Loss DEL dbSNP153 30..33 33 - - - 101430 RMVar_ID_101430 Human_SNP_ID_23728907 m1A Human chr1 + 95134160 95134160 95134160 ATAAAGGTTCATGGGTGGGTAAGGTGGCATGGAAGACATGCCATTCCAGGTGAAGATAATGGACT ATAAAGGTTCATGGGTGGGTAAGGTGGCATGGGAGACATGCCATTCCAGGTGAAGATAATGGACT A G TLCD4,TLCD4-RWDD3,AC092802.4 Ensembl:ENSG00000152078,Ensembl:ENSG00000271092,Ensembl:ENSG00000231992 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:95134143..95134343 26863196 MeRIP-seq:(Medium) rs1359972487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24325 101431 RMVar_ID_101431 Human_SNP_ID_23740108 m1A Human chr1 + 95182974 95182974 95182974 GGATCAAAGAGTATGTCTTAGGGGTAGGGTGGATAGATGTAGAGGATGTTGAGTGTCTGGGAGAG GGATCAAAGAGTATGTCTTAGGGGTAGGGTGGTTAGATGTAGAGGATGTTGAGTGTCTGGGAGAG A T TLCD4,TLCD4-RWDD3 Ensembl:ENSG00000152078,Ensembl:ENSG00000271092 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:95182938..95183003 26863196 MeRIP-seq:(Medium) rs1419202062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23422739 RMVar_hsa_circ_327348,RMVar_hsa_circ_134725,RMVar_hsa_circ_95568,RMVar_hsa_circ_134727 101432 RMVar_ID_101432 Human_SNP_ID_23751448 m1A Human chr1 - 95234274 95234273 95234274 TCAGCACCTCCCACTCGTGGGGCCTGCAGAAAATCGCGGCCAGGACCGAGAGCTCCTCCTGCACA TCAGCACCTCCCACTCGTGGGGCCTGCAGAAA_TCGCGGCCAGGACCGAGAGCTCCTCCTGCACA AT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:95234225..95234316 26863196 MeRIP-seq:(Medium) rs1557716690 Functional Loss DEL dbSNP153 33..33 33 - - - 101433 RMVar_ID_101433 Human_SNP_ID_23751468 m1A Human chr1 + 95234322 95234322 95234322 CGAGTGGGAGGTGCTGAGCCGCTCAGGTGACTACCCGCGCGCGGGAGGGACAGGGCGCCCTCAGG CGAGTGGGAGGTGCTGAGCCGCTCAGGTGACTGCCCGCGCGCGGGAGGGACAGGGCGCCCTCAGG A G RWDD3,TLCD4-RWDD3 Ensembl:ENSG00000122481,Ensembl:ENSG00000271092 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:95234321..95234453 32194978 MeRIP-seq:(Medium) rs779189549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854940,Human_RBP_ID_5335657,Human_RBP_ID_9319040,Human_RBP_ID_19038666 101434 RMVar_ID_101434 Human_SNP_ID_24122641 m1A Human chr1 + 96751374 96751374 96751374 ATTTGACATTTAAGTGAAAGGCTTTTAGATTAATATTTTTAAATTTAAAGATGTCTTATGCTAAT ATTTGACATTTAAGTGAAAGGCTTTTAGATTACTATTTTTAAATTTAAAGATGTCTTATGCTAAT A C PTBP2 Ensembl:ENSG00000117569 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:96751372..96751440 26863196 MeRIP-seq:(Medium) rs762946124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5887999,Human_RBP_ID_8322898,Human_RBP_ID_11170148 101435 RMVar_ID_101435 Human_SNP_ID_24319658 m1A Human chr1 - 97529757 97529739 97529757 GAAAAAGAGAAAGAAAGAAGAAAGAGAAAGAAAGAAAGGAAGGGAAAGAAGGAAAGAAAGGAAAG GAAAAAGAGAAAGAAAGAAGAAAGAGAAAGAA__________________GGAAAGAAAGGAAAG CTTCTTTCCCTTCCTTTCT C DPYD Ensembl:ENSG00000188641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:97529730..97529962 26863196 MeRIP-seq:(Medium) rs1280346246 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_9596,RMVar_hsa_circ_12215,RMVar_hsa_circ_98074,RMVar_hsa_circ_134749,RMVar_hsa_circ_364488,RMVar_hsa_circ_265876,RMVar_hsa_circ_34276,RMVar_hsa_circ_15459,RMVar_hsa_circ_101324,RMVar_hsa_circ_48401,RMVar_hsa_circ_73772,RMVar_hsa_circ_134756,RMVar_hsa_circ_11570,RMVar_hsa_circ_134753,RMVar_hsa_circ_310660,RMVar_hsa_circ_319092,RMVar_hsa_circ_282650,RMVar_hsa_circ_81211,RMVar_hsa_circ_3116,RMVar_hsa_circ_324275,RMVar_hsa_circ_334502,RMVar_hsa_circ_354303,RMVar_hsa_circ_357020,RMVar_hsa_circ_356913,RMVar_hsa_circ_348998,RMVar_hsa_circ_307416,RMVar_hsa_circ_30331,RMVar_hsa_circ_267198,RMVar_hsa_circ_73773,RMVar_hsa_circ_289670,RMVar_hsa_circ_331506,RMVar_hsa_circ_351661,RMVar_hsa_circ_364464,RMVar_hsa_circ_337591,RMVar_hsa_circ_40369,RMVar_hsa_circ_134764,RMVar_hsa_circ_288479,RMVar_hsa_circ_323853,RMVar_hsa_circ_353694,RMVar_hsa_circ_359359,RMVar_hsa_circ_333484,RMVar_hsa_circ_310431,RMVar_hsa_circ_279015,RMVar_hsa_circ_284256,RMVar_hsa_circ_271694,RMVar_hsa_circ_134766,RMVar_hsa_circ_134768,RMVar_hsa_circ_11745,RMVar_hsa_circ_134767,RMVar_hsa_circ_134765 101436 RMVar_ID_101436 Human_SNP_ID_24319663 m1A Human chr1 - 97529755 97529751 97529755 AAAAGAGAAAGAAAGAAGAAAGAGAAAGAAAGAAAGGAAGGGAAAGAAGGAAAGAAAGGAAAGAA AAAAGAGAAAGAAAGAAGAAAGAGAAAGAAAG____GAAGGGAAAGAAGGAAAGAAAGGAAAGAA CCTTT C DPYD Ensembl:ENSG00000188641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:97529711..97529940 26863196 MeRIP-seq:(Medium) rs781470193 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_9596,RMVar_hsa_circ_12215,RMVar_hsa_circ_98074,RMVar_hsa_circ_134749,RMVar_hsa_circ_364488,RMVar_hsa_circ_265876,RMVar_hsa_circ_34276,RMVar_hsa_circ_15459,RMVar_hsa_circ_101324,RMVar_hsa_circ_48401,RMVar_hsa_circ_73772,RMVar_hsa_circ_134756,RMVar_hsa_circ_11570,RMVar_hsa_circ_134753,RMVar_hsa_circ_310660,RMVar_hsa_circ_319092,RMVar_hsa_circ_282650,RMVar_hsa_circ_81211,RMVar_hsa_circ_3116,RMVar_hsa_circ_324275,RMVar_hsa_circ_334502,RMVar_hsa_circ_354303,RMVar_hsa_circ_357020,RMVar_hsa_circ_356913,RMVar_hsa_circ_348998,RMVar_hsa_circ_307416,RMVar_hsa_circ_30331,RMVar_hsa_circ_267198,RMVar_hsa_circ_73773,RMVar_hsa_circ_289670,RMVar_hsa_circ_331506,RMVar_hsa_circ_351661,RMVar_hsa_circ_364464,RMVar_hsa_circ_337591,RMVar_hsa_circ_40369,RMVar_hsa_circ_134764,RMVar_hsa_circ_288479,RMVar_hsa_circ_323853,RMVar_hsa_circ_353694,RMVar_hsa_circ_359359,RMVar_hsa_circ_333484,RMVar_hsa_circ_310431,RMVar_hsa_circ_279015,RMVar_hsa_circ_284256,RMVar_hsa_circ_271694,RMVar_hsa_circ_134766,RMVar_hsa_circ_134768,RMVar_hsa_circ_11745,RMVar_hsa_circ_134767,RMVar_hsa_circ_134765 101437 RMVar_ID_101437 Human_SNP_ID_24319666 m1A Human chr1 - 97529757 97529752 97529758 GAAAAAGAGAAAGAAAGAAGAAAGAGAAAGAAAGAAAGGAAGGGAAAGAAGGAAAGAAAGGAAAG GAAAAAGAGAAAGAAAGAAGAAAGAGAAAGA______GGAAGGGAAAGAAGGAAAGAAAGGAAAG CTTTCTT C DPYD Ensembl:ENSG00000188641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:97529730..97529962 26863196 MeRIP-seq:(Medium) rs1439510519 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_9596,RMVar_hsa_circ_12215,RMVar_hsa_circ_98074,RMVar_hsa_circ_134749,RMVar_hsa_circ_364488,RMVar_hsa_circ_265876,RMVar_hsa_circ_34276,RMVar_hsa_circ_15459,RMVar_hsa_circ_101324,RMVar_hsa_circ_48401,RMVar_hsa_circ_73772,RMVar_hsa_circ_134756,RMVar_hsa_circ_11570,RMVar_hsa_circ_134753,RMVar_hsa_circ_310660,RMVar_hsa_circ_319092,RMVar_hsa_circ_282650,RMVar_hsa_circ_81211,RMVar_hsa_circ_3116,RMVar_hsa_circ_324275,RMVar_hsa_circ_334502,RMVar_hsa_circ_354303,RMVar_hsa_circ_357020,RMVar_hsa_circ_356913,RMVar_hsa_circ_348998,RMVar_hsa_circ_307416,RMVar_hsa_circ_30331,RMVar_hsa_circ_267198,RMVar_hsa_circ_73773,RMVar_hsa_circ_289670,RMVar_hsa_circ_331506,RMVar_hsa_circ_351661,RMVar_hsa_circ_364464,RMVar_hsa_circ_337591,RMVar_hsa_circ_40369,RMVar_hsa_circ_134764,RMVar_hsa_circ_288479,RMVar_hsa_circ_323853,RMVar_hsa_circ_353694,RMVar_hsa_circ_359359,RMVar_hsa_circ_333484,RMVar_hsa_circ_310431,RMVar_hsa_circ_279015,RMVar_hsa_circ_284256,RMVar_hsa_circ_271694,RMVar_hsa_circ_134766,RMVar_hsa_circ_134768,RMVar_hsa_circ_11745,RMVar_hsa_circ_134767,RMVar_hsa_circ_134765 101438 RMVar_ID_101438 Human_SNP_ID_24319667 m1A Human chr1 - 97529755 97529753 97529756 AAAAGAGAAAGAAAGAAGAAAGAGAAAGAAAGAAAGGAAGGGAAAGAAGGAAAGAAAGGAAAGAA AAAAGAGAAAGAAAGAAGAAAGAGAAAGAAA___AGGAAGGGAAAGAAGGAAAGAAAGGAAAGAA TTTC T DPYD Ensembl:ENSG00000188641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:97529711..97529940 26863196 MeRIP-seq:(Medium) rs1353449228 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_9596,RMVar_hsa_circ_12215,RMVar_hsa_circ_98074,RMVar_hsa_circ_134749,RMVar_hsa_circ_364488,RMVar_hsa_circ_265876,RMVar_hsa_circ_34276,RMVar_hsa_circ_15459,RMVar_hsa_circ_101324,RMVar_hsa_circ_48401,RMVar_hsa_circ_73772,RMVar_hsa_circ_134756,RMVar_hsa_circ_11570,RMVar_hsa_circ_134753,RMVar_hsa_circ_310660,RMVar_hsa_circ_319092,RMVar_hsa_circ_282650,RMVar_hsa_circ_81211,RMVar_hsa_circ_3116,RMVar_hsa_circ_324275,RMVar_hsa_circ_334502,RMVar_hsa_circ_354303,RMVar_hsa_circ_357020,RMVar_hsa_circ_356913,RMVar_hsa_circ_348998,RMVar_hsa_circ_307416,RMVar_hsa_circ_30331,RMVar_hsa_circ_267198,RMVar_hsa_circ_73773,RMVar_hsa_circ_289670,RMVar_hsa_circ_331506,RMVar_hsa_circ_351661,RMVar_hsa_circ_364464,RMVar_hsa_circ_337591,RMVar_hsa_circ_40369,RMVar_hsa_circ_134764,RMVar_hsa_circ_288479,RMVar_hsa_circ_323853,RMVar_hsa_circ_353694,RMVar_hsa_circ_359359,RMVar_hsa_circ_333484,RMVar_hsa_circ_310431,RMVar_hsa_circ_279015,RMVar_hsa_circ_284256,RMVar_hsa_circ_271694,RMVar_hsa_circ_134766,RMVar_hsa_circ_134768,RMVar_hsa_circ_11745,RMVar_hsa_circ_134767,RMVar_hsa_circ_134765 101439 RMVar_ID_101439 Human_SNP_ID_24447082 m1A Human chr1 - 98045102 98045102 98045102 TTTGTTTGTTTCAAATATTAATGGACGATAAAACAACACGGATTTGTCACCTCCTAGCGAAGAGG TTTGTTTGTTTCAAATATTAATGGACGATAAAGCAACACGGATTTGTCACCTCCTAGCGAAGAGG T C MIR137HG Ensembl:ENSG00000225206 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:98045051..98045201 32194978 MeRIP-seq:(Medium) rs1377448677 Functional Loss SNV dbSNP153 33..33 33 - - - 101440 RMVar_ID_101440 Human_SNP_ID_24606489 m1A Human chr1 - 98661836 98661836 98661836 AGCACCTCCGCCTGCAGCAGGGCGGAAGAGCCACTGCTGCCCGGAAAGGGGGCGCCGCCCCCCGG AGCACCTCCGCCTGCAGCAGGGCGGAAGAGCCGCTGCTGCCCGGAAAGGGGGCGCCGCCCCCCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:98661747..98661877 26863410 MeRIP-seq:(Medium) rs9728148 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 101441 RMVar_ID_101441 Human_SNP_ID_24844298 m1A Human chr1 + 99646201 99646201 99646201 GTCGGGAATTTCTCTATTTCTCCACTGGTGCAAAGAGCGGATTTCTCCCTGCTTCTCTTCTGTCA GTCGGGAATTTCTCTATTTCTCCACTGGTGCAGAGAGCGGATTTCTCCCTGCTTCTCTTCTGTCA A G PALMD Ensembl:ENSG00000099260 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:99646150..99646410 26863196 MeRIP-seq:(Medium) rs566019235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78094,RMVar_hsa_circ_112420,RMVar_hsa_circ_134835,RMVar_hsa_circ_134836 101442 RMVar_ID_101442 Human_SNP_ID_24854788 m1A Human chr1 - 99689571 99689571 99689571 TCAATCACAACCAGCTCAGCATGGATGATCCCATCATATCCTGTCAGAAACTTCTTATCTTCTTC TCAATCACAACCAGCTCAGCATGGATGATCCCGTCATATCCTGTCAGAAACTTCTTATCTTCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:99689520..99689766 26863196 MeRIP-seq:(Medium) rs374860117 Functional Loss SNV dbSNP153 33..33 33 - - - 101443 RMVar_ID_101443 Human_SNP_ID_24854799 m1A Human chr1 - 99689607 99689607 99689607 TTCTCTGCTTCTCCTTCATCCTCCTCCTCCTCATCATCAATCACAACCAGCTCAGCATGGATGAT TTCTCTGCTTCTCCTTCATCCTCCTCCTCCTCGTCATCAATCACAACCAGCTCAGCATGGATGAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:99689563..99689680 26863196 MeRIP-seq:(Medium) rs756366841 Functional Loss SNV dbSNP153 33..33 33 - - - 101444 RMVar_ID_101444 Human_SNP_ID_24854800 m1A Human chr1 - 99689607 99689607 99689607 TTCTCTGCTTCTCCTTCATCCTCCTCCTCCTCATCATCAATCACAACCAGCTCAGCATGGATGAT TTCTCTGCTTCTCCTTCATCCTCCTCCTCCTCCTCATCAATCACAACCAGCTCAGCATGGATGAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:99689563..99689680 26863196 MeRIP-seq:(Medium) rs756366841 Functional Loss SNV dbSNP153 33..33 33 - - - 101445 RMVar_ID_101445 Human_SNP_ID_24854843 m1A Human chr1 + 99689678 99689678 99689678 CTACCACCCCATAGCTCCCCATAGTCAGGTGTACCAGCCAGCCAAACCAACACCACTTCCTAGAA CTACCACCCCATAGCTCCCCATAGTCAGGTGTCCCAGCCAGCCAAACCAACACCACTTCCTAGAA A C PALMD Ensembl:ENSG00000099260 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:99689632..99689754 26863196 MeRIP-seq:(Medium) rs1315478735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9501,RMVar_hsa_circ_112420,RMVar_hsa_circ_134836,RMVar_hsa_circ_8726,RMVar_hsa_circ_134837,RMVar_hsa_circ_134839 101446 RMVar_ID_101446 Human_SNP_ID_24892902 m1A Human chr1 - 99850195 99850195 99850195 AGCGCCGAGGCAGCTGGGTGAGAAGCAGGCAGAGTCTCAGCGACTTCGCCTCGCGCGGGTTCCTG AGCGCCGAGGCAGCTGGGTGAGAAGCAGGCAGTGTCTCAGCGACTTCGCCTCGCGCGGGTTCCTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:99850150..99850314 26863196 MeRIP-seq:(Medium) rs1355307341 Functional Loss SNV dbSNP153 33..33 33 - - - 101447 RMVar_ID_101447 Human_SNP_ID_24892915 m1A Human chr1 - 99850235 99850235 99850235 GCCGTGAAGGGCAAAGGGAGGGGCGGCGAGCGACCGGGGCAGCGCCGAGGCAGCTGGGTGAGAAG GCCGTGAAGGGCAAAGGGAGGGGCGGCGAGCGCCCGGGGCAGCGCCGAGGCAGCTGGGTGAGAAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:99850121..99850383 26863196 MeRIP-seq:(Medium) rs1356343124 Functional Loss SNV dbSNP153 33..33 33 - - - 101448 RMVar_ID_101448 Human_SNP_ID_24922677 m1A Human chr1 - 99970067 99970067 99970067 CCCAGGCTGCCGAGTCCGCTGGGTCCTACGCGACCGCTGACCCGCAGCGCCGCCGGCTCCCGTCG CCCAGGCTGCCGAGTCCGCTGGGTCCTACGCGGCCGCTGACCCGCAGCGCCGCCGGCTCCCGTCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:99970018..99970492 26863196 MeRIP-seq:(Medium) rs1447943698 Functional Loss SNV dbSNP153 33..33 33 - - - 101449 RMVar_ID_101449 Human_SNP_ID_24922680 m1A Human chr1 + 99970076 99970076 99970076 CCGGCGGCGCTGCGGGTCAGCGGTCGCGTAGGACCCAGCGGACTCGGCAGCCTGGGGCGCCCGGC CCGGCGGCGCTGCGGGTCAGCGGTCGCGTAGGTCCCAGCGGACTCGGCAGCCTGGGGCGCCCGGC A T AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:99970026..99975018;chr1:99970026..99970425 26863196 MeRIP-seq:(Medium) rs897923552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223782,Human_RBP_ID_4072945,Human_RBP_ID_18415011 Human_Splice_Rec_99901,Human_Splice_Rec_99915,Human_Splice_Rec_99931,Human_Splice_Rec_99945,Human_Splice_Rec_99955,Human_Splice_Rec_99965,Human_Splice_Rec_99977,Human_Splice_Rec_100003,Human_Splice_Rec_100019,Human_Splice_Rec_100031,Human_Splice_Rec_100043,Human_Splice_Rec_100055,Human_Splice_Rec_100063,Human_Splice_Rec_100075,Human_Splice_Rec_100081,Human_Splice_Rec_100097,Human_Splice_Rec_100109,Human_Splice_Rec_100121,Human_Splice_Rec_100129,Human_Splice_Rec_100181,Human_Splice_Rec_100219,Human_Splice_Rec_100249,Human_Splice_Rec_100281,Human_Splice_Rec_100311,Human_Splice_Rec_100339,Human_Splice_Rec_100369,Human_Splice_Rec_100403 101450 RMVar_ID_101450 Human_SNP_ID_24931489 m1A Human chr1 + 100009628 100009628 100009628 GGAGAAATACTGAAGGAATGGAGAGGAGTTAGAAAGCATGACAGGGACCTAAACTGTCAGGTTAA GGAGAAATACTGAAGGAATGGAGAGGAGTTAGGAAGCATGACAGGGACCTAAACTGTCAGGTTAA A G AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:100009584..100009788 26863196 MeRIP-seq:(Medium) rs746750691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221593 RMVar_hsa_circ_23175,RMVar_hsa_circ_286523,RMVar_hsa_circ_323796,RMVar_hsa_circ_315123,RMVar_hsa_circ_72796,RMVar_hsa_circ_134884,RMVar_hsa_circ_134885,RMVar_hsa_circ_134886,RMVar_hsa_circ_286247,RMVar_hsa_circ_293203,RMVar_hsa_circ_315220,RMVar_hsa_circ_41209,RMVar_hsa_circ_75169,RMVar_hsa_circ_134888,RMVar_hsa_circ_134889,RMVar_hsa_circ_134890,RMVar_hsa_circ_338448,RMVar_hsa_circ_134887,RMVar_hsa_circ_362613,RMVar_hsa_circ_302919,RMVar_hsa_circ_134892,RMVar_hsa_circ_53108,RMVar_hsa_circ_134891 101451 RMVar_ID_101451 Human_SNP_ID_24937963 m1A Human chr1 + 100038151 100038151 100038151 GGCGGCGGGCGCCCAGAGCGGCTCGGCCCGGCAGTAGTGGTGGGACGGCACTAGCTGCTGGGGCC GGCGGCGGGCGCCCAGAGCGGCTCGGCCCGGCCGTAGTGGTGGGACGGCACTAGCTGCTGGGGCC A C MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:100038101..100038200;chr1:100038101..100038325;chr1:100038101..100038357 26863196 MeRIP-seq:(Medium) rs1351500571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224266,Human_RBP_ID_4072946,Human_RBP_ID_5311781,Human_RBP_ID_22429490,Human_RBP_ID_23318154,Human_RBP_ID_24360338 RMVar_hsa_circ_23175,RMVar_hsa_circ_72796,RMVar_hsa_circ_41209,RMVar_hsa_circ_75169,RMVar_hsa_circ_134890,RMVar_hsa_circ_338448,RMVar_hsa_circ_362613,RMVar_hsa_circ_362253,RMVar_hsa_circ_134891,RMVar_hsa_circ_40648 101452 RMVar_ID_101452 Human_SNP_ID_24937993 m1A Human chr1 + 100038214 100038214 100038214 CCTGCCGCCCCGGGAGTGGCTGCAGCAGCGCCAGGAATCGAGGATGGTAAAATGACCCAGGGGAA CCTGCCGCCCCGGGAGTGGCTGCAGCAGCGCCGGGAATCGAGGATGGTAAAATGACCCAGGGGAA A G MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:100038101..100038300 26863196 MeRIP-seq:(Medium) rs368190066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072946,Human_RBP_ID_8952826,Human_RBP_ID_10488068,Human_RBP_ID_18545910,Human_RBP_ID_22428485 RMVar_hsa_circ_23175,RMVar_hsa_circ_72796,RMVar_hsa_circ_41209,RMVar_hsa_circ_75169,RMVar_hsa_circ_134890,RMVar_hsa_circ_338448,RMVar_hsa_circ_362613,RMVar_hsa_circ_362253,RMVar_hsa_circ_134891,RMVar_hsa_circ_40648 101453 RMVar_ID_101453 Human_SNP_ID_24945648 m1A Human chr1 + 100068523 100068523 100068523 CAAGATTCCATAGTGCTGCTGATCTGCATTACAGTGTTTCTCTCCTACCTACCGGAGGCAGGCCA CAAGATTCCATAGTGCTGCTGATCTGCATTACGGTGTTTCTCTCCTACCTACCGGAGGCAGGCCA A G MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:100068135..100068523 32194978 MeRIP-seq:(Medium) rs777531037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_318815,Human_RBP_ID_17444163 Human_Splice_Rec_100208,Human_Splice_Rec_100209,Human_Splice_Rec_100240,Human_Splice_Rec_100241,Human_Splice_Rec_100270,Human_Splice_Rec_100271,Human_Splice_Rec_100300,Human_Splice_Rec_100301,Human_Splice_Rec_100334,Human_Splice_Rec_100335,Human_Splice_Rec_100360,Human_Splice_Rec_100361,Human_Splice_Rec_100392,Human_Splice_Rec_100393,Human_Splice_Rec_100426,Human_Splice_Rec_100427,Human_Splice_Rec_100448,Human_Splice_Rec_100449 Human_miRNA_ID_285697,Human_miRNA_ID_285698,Human_miRNA_ID_523730,Human_miRNA_ID_523731,Human_miRNA_ID_2058589,Human_miRNA_ID_2058590,Human_miRNA_ID_2135368,Human_miRNA_ID_2135369,Human_miRNA_ID_2183983,Human_miRNA_ID_2183984,Human_miRNA_ID_2608041,Human_miRNA_ID_2608042,Human_miRNA_ID_2664170,Human_miRNA_ID_2664171 RMVar_hsa_circ_23175,RMVar_hsa_circ_75169,RMVar_hsa_circ_310522,RMVar_hsa_circ_332601,RMVar_hsa_circ_299828,RMVar_hsa_circ_289576,RMVar_hsa_circ_93532,RMVar_hsa_circ_134897,RMVar_hsa_circ_134898,RMVar_hsa_circ_134899,RMVar_hsa_circ_279504,RMVar_hsa_circ_293291,RMVar_hsa_circ_303864,RMVar_hsa_circ_300274,RMVar_hsa_circ_134901,RMVar_hsa_circ_307687,RMVar_hsa_circ_376281,RMVar_hsa_circ_115531,RMVar_hsa_circ_134902,RMVar_hsa_circ_134904,RMVar_hsa_circ_30827,RMVar_hsa_circ_134903,RMVar_hsa_circ_134907,RMVar_hsa_circ_121018,RMVar_hsa_circ_63544,RMVar_hsa_circ_285472 101454 RMVar_ID_101454 Human_SNP_ID_24961402 m1A Human chr1 - 100133232 100133232 100133232 CATCCTGCAGAACCGTTTCTTCTTTTCCACATAGTAACCGCATCTACCCTCAGCTGGAAAACCAG CATCCTGCAGAACCGTTTCTTCTTTTCCACATTGTAACCGCATCTACCCTCAGCTGGAAAACCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:100133181..100133349 26863196 MeRIP-seq:(Medium) rs758958406 Functional Loss SNV dbSNP153 33..33 33 - - - 101455 RMVar_ID_101455 Human_SNP_ID_24961403 m1A Human chr1 - 100133232 100133232 100133232 CATCCTGCAGAACCGTTTCTTCTTTTCCACATAGTAACCGCATCTACCCTCAGCTGGAAAACCAG CATCCTGCAGAACCGTTTCTTCTTTTCCACATGGTAACCGCATCTACCCTCAGCTGGAAAACCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:100133181..100133349 26863196 MeRIP-seq:(Medium) rs758958406 Functional Loss SNV dbSNP153 33..33 33 - - - 101456 RMVar_ID_101456 Human_SNP_ID_24961415 m1A Human chr1 - 100133253 100133253 100133253 TCTTTTCCCTGCGGCCACCACCATCCTGCAGAACCGTTTCTTCTTTTCCACATAGTAACCGCATC TCTTTTCCCTGCGGCCACCACCATCCTGCAGAGCCGTTTCTTCTTTTCCACATAGTAACCGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:100133203..100133342 26863196 MeRIP-seq:(Medium) rs757056954 Functional Loss SNV dbSNP153 33..33 33 - - - 101457 RMVar_ID_101457 Human_SNP_ID_24984983 m1A Human chr1 - 100238249 100238237 100238250 CAAGGAAAGGAAGGGAGGAAAGGAAGGGAGGAAAGGAAGTGAGGGAAGGAAGGGAGGAAAGGAAG CAAGGAAAGGAAGGGAGGAAAGGAAGGGAGG_____________GAAGGAAGGGAGGAAAGGAAG CCCTCACTTCCTTT C DBT Ensembl:ENSG00000137992 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:100238247..100238316 26863196 MeRIP-seq:(Medium) rs1200244863 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_295112,RMVar_hsa_circ_134930,RMVar_hsa_circ_308498,RMVar_hsa_circ_304399,RMVar_hsa_circ_307057,RMVar_hsa_circ_134936,RMVar_hsa_circ_340839 101458 RMVar_ID_101458 Human_SNP_ID_25145709 m1A Human chr1 + 100895028 100895028 100895028 GACCACCTTCCCTCAGCCAAACAACTTCCCTGAAAGGCGCCCGAAGGAGCCTTCCCATCCACCGC GACCACCTTCCCTCAGCCAAACAACTTCCCTGCAAGGCGCCCGAAGGAGCCTTCCCATCCACCGC A C AC104506.1 Ensembl:ENSG00000273204 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:100894991..100895092;chr1:100894992..100895076 26863196 MeRIP-seq:(Medium) rs995278020 Functional Loss SNV dbSNP153 33..33 33 - - - 101459 RMVar_ID_101459 Human_SNP_ID_25175337 m1A Human chr1 + 101025944 101025944 101025944 AGAAACCCGCCGGCTGCTGGGGCAGGGCGGCGAAAGGTCAGTCGGCCGAGAGGAGTCCGTGGAGC AGAAACCCGCCGGCTGCTGGGGCAGGGCGGCGGAAGGTCAGTCGGCCGAGAGGAGTCCGTGGAGC A G AC093157.1 Ensembl:ENSG00000233184 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:101025893..101026018 26863196 MeRIP-seq:(Medium) rs181024251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4076916,Human_RBP_ID_5541239,Human_RBP_ID_18415014 Human_Splice_Rec_101451 101460 RMVar_ID_101460 Human_SNP_ID_11632435 m1A Human chr1 + 45002671 45002671 45002671 GCAGGGGTGTGCATAGCTCTAGGAACAGGTTTAAGGTCTAGGCTTTAGAGTTGGGGAAAGGGGAG GCAGGGGTGTGCATAGCTCTAGGAACAGGTTTCAGGTCTAGGCTTTAGAGTTGGGGAAAGGGGAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:45002642..45002775 26863196 MeRIP-seq:(Medium) rs909884581 Functional Loss SNV dbSNP153 33..33 33 - - - 101461 RMVar_ID_101461 Human_SNP_ID_11632478 m1A Human chr1 - 45002845 45002845 45002845 CCACCACCTTCCCTGACTCAGAACCCACATCCACTCAATGTGAACTCTACTACCACGACCTCCCC CCACCACCTTCCCTGACTCAGAACCCACATCCGCTCAATGTGAACTCTACTACCACGACCTCCCC T C HECTD3 Ensembl:ENSG00000126107 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45002796..45002957 26863196 MeRIP-seq:(Medium) rs958830076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17453316 Human_miRNA_ID_1082821,Human_miRNA_ID_2020392,Human_miRNA_ID_2258943,Human_miRNA_ID_2261984,Human_miRNA_ID_2265051,Human_miRNA_ID_2505735,Human_miRNA_ID_3042312 RMVar_hsa_circ_101535,RMVar_hsa_circ_125850,RMVar_hsa_circ_111903,RMVar_hsa_circ_132465,RMVar_hsa_circ_132466,RMVar_hsa_circ_132467 101462 RMVar_ID_101462 Human_SNP_ID_11633126 m1A Human chr1 - 45004772 45004772 45004772 GAAGCTCCTGGAAGTGATGGAAGGAATGGACAAGGAGACGTTTGAGTTCAAGTTTGGGAAGGAAC GAAGCTCCTGGAAGTGATGGAAGGAATGGACAGGGAGACGTTTGAGTTCAAGTTTGGGAAGGAAC T C HECTD3 Ensembl:ENSG00000126107 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:45004721..45004818 26863196 MeRIP-seq:(Medium) rs373467949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3935993,Human_RBP_ID_18968265,Human_RBP_ID_22559001 Human_Splice_Rec_62578,Human_Splice_Rec_62618,Human_Splice_Rec_62632,Human_Splice_Rec_62646 RMVar_hsa_circ_125850,RMVar_hsa_circ_81986,RMVar_hsa_circ_109195,RMVar_hsa_circ_132467,RMVar_hsa_circ_118474,RMVar_hsa_circ_116999,RMVar_hsa_circ_132468,RMVar_hsa_circ_132469,RMVar_hsa_circ_132471,RMVar_hsa_circ_101189,RMVar_hsa_circ_132470,RMVar_hsa_circ_132472 101463 RMVar_ID_101463 Human_SNP_ID_11635786 m1A Human chr1 - 45012287 45012287 45012287 CGGCTAGCCACACCGCGTGCTCTGGAGAACTCACCCCAACCCATTCGCTTCCATGGTCAGCTGTC CGGCTAGCCACACCGCGTGCTCTGGAGAACTCGCCCCAACCCATTCGCTTCCATGGTCAGCTGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:45012245..45012749;chr1:45012226..45012324 26863196 MeRIP-seq:(Medium) rs1287506370 Functional Loss SNV dbSNP153 33..33 33 - - - 101464 RMVar_ID_101464 Human_SNP_ID_11635933 m1A Human chr1 - 45012824 45012824 45012824 CTGGGGAAAGCGCGGGTTCATAAGGCCGATTCAGTCCAGGACCGCTATCTACCTCCTCCAGGCCA CTGGGGAAAGCGCGGGTTCATAAGGCCGATTCGGTCCAGGACCGCTATCTACCTCCTCCAGGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45012821..45013025 26863196 MeRIP-seq:(Medium) rs983991753 Functional Loss SNV dbSNP153 33..33 33 - - - 101465 RMVar_ID_101465 Human_SNP_ID_11635934 m1A Human chr1 - 45012824 45012824 45012824 CTGGGGAAAGCGCGGGTTCATAAGGCCGATTCAGTCCAGGACCGCTATCTACCTCCTCCAGGCCA CTGGGGAAAGCGCGGGTTCATAAGGCCGATTCCGTCCAGGACCGCTATCTACCTCCTCCAGGCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45012821..45013025 26863196 MeRIP-seq:(Medium) rs983991753 Functional Loss SNV dbSNP153 33..33 33 - - - 101466 RMVar_ID_101466 Human_SNP_ID_11636077 m1A Human chr1 + 45013160 45013160 45013160 GTATGCAGAGTTTAGGGAAACCCGGGCTGCCCAGGACTTTTTCAGCACGTGTCGCTCTCCTGAGG GTATGCAGAGTTTAGGGAAACCCGGGCTGCCCGGGACTTTTTCAGCACGTGTCGCTCTCCTGAGG A G UROD Ensembl:ENSG00000126088 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45012926..45013161 32194978 MeRIP-seq:(Medium) rs199597323 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5457734,Human_RBP_ID_5830117,Human_RBP_ID_8312590,Human_RBP_ID_11005028,Human_RBP_ID_17752366,Human_RBP_ID_18187116,Human_RBP_ID_18430491,Human_RBP_ID_22427215,Human_RBP_ID_23122751,Human_RBP_ID_27183979,Human_RBP_ID_27399327,Human_RBP_ID_27555500 Human_Splice_Rec_62662,Human_Splice_Rec_62663,Human_Splice_Rec_62678,Human_Splice_Rec_62679,Human_Splice_Rec_62686,Human_Splice_Rec_62687,Human_Splice_Rec_62704,Human_Splice_Rec_62708,Human_Splice_Rec_62709,Human_Splice_Rec_62724,Human_Splice_Rec_62725,Human_Splice_Rec_62740,Human_Splice_Rec_62741,Human_Splice_Rec_62756,Human_Splice_Rec_62757,Human_Splice_Rec_62762,Human_Splice_Rec_62763,Human_Splice_Rec_62774,Human_Splice_Rec_62775,Human_Splice_Rec_62790,Human_Splice_Rec_62802,Human_Splice_Rec_62803,Human_Splice_Rec_62814,Human_Splice_Rec_62815,Human_Splice_Rec_62832,Human_Splice_Rec_62833,Human_Splice_Rec_62842,Human_Splice_Rec_62852,Human_Splice_Rec_62853,Human_Splice_Rec_62860,Human_Splice_Rec_62866,Human_Splice_Rec_62867,Human_Splice_Rec_62878,Human_Splice_Rec_62879,Human_Splice_Rec_62900,Human_Splice_Rec_62901,Human_Splice_Rec_62910,Human_Splice_Rec_62911,Human_Splice_Rec_62916,Human_Splice_Rec_62922,Human_Splice_Rec_62923 RMVar_hsa_circ_7870 101467 RMVar_ID_101467 Human_SNP_ID_11636091 m1A Human chr1 - 45013188 45013188 45013188 CTCACCTGCAGAGTCAGTTCACAGCAGGCCTCAGGAGAGCGACACGTGCTGAAAAAGTCCTGGGC CTCACCTGCAGAGTCAGTTCACAGCAGGCCTCGGGAGAGCGACACGTGCTGAAAAAGTCCTGGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45012945..45013375 32194978 MeRIP-seq:(Medium) rs765472159 Functional Loss SNV dbSNP153 33..33 33 - - - 101468 RMVar_ID_101468 Human_SNP_ID_11636103 m1A Human chr1 - 45013217 45013217 45013217 GCATAAATCTTTCCCTCTTTTGTGGACCCCTCACCTGCAGAGTCAGTTCACAGCAGGCCTCAGGA GCATAAATCTTTCCCTCTTTTGTGGACCCCTCGCCTGCAGAGTCAGTTCACAGCAGGCCTCAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45013192..45013284 26863196 MeRIP-seq:(Medium) rs1001840437 Functional Loss SNV dbSNP153 33..33 33 - - - 101469 RMVar_ID_101469 Human_SNP_ID_11636270 m1A Human chr1 + 45013680 45013680 45013680 CCATTAAGAGAAGAGCAGGACCTAGAACGCCTACGGGATCCAGAAGTGGTAGCCTCTGAGCTAGG CCATTAAGAGAAGAGCAGGACCTAGAACGCCTGCGGGATCCAGAAGTGGTAGCCTCTGAGCTAGG A G UROD Ensembl:ENSG00000126088 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45013576..45014075 32194978 MeRIP-seq:(Medium) rs1374785892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1432112,Human_RBP_ID_1748815,Human_RBP_ID_3935997,Human_RBP_ID_4096689,Human_RBP_ID_9356245,Human_RBP_ID_11005032,Human_RBP_ID_18968267,Human_RBP_ID_22430560,Human_RBP_ID_23205915,Human_RBP_ID_26388140 Human_Splice_Rec_62666,Human_Splice_Rec_62682,Human_Splice_Rec_62690,Human_Splice_Rec_62710,Human_Splice_Rec_62728,Human_Splice_Rec_62744,Human_Splice_Rec_62778,Human_Splice_Rec_62792,Human_Splice_Rec_62818,Human_Splice_Rec_62844,Human_Splice_Rec_62862,Human_Splice_Rec_62870,Human_Splice_Rec_62892,Human_Splice_Rec_62904,Human_Splice_Rec_62914,Human_Splice_Rec_62926 RMVar_hsa_circ_92556,RMVar_hsa_circ_119027,RMVar_hsa_circ_373839,RMVar_hsa_circ_132477,RMVar_hsa_circ_132478,RMVar_hsa_circ_132476,RMVar_hsa_circ_132479,RMVar_hsa_circ_375279 101470 RMVar_ID_101470 Human_SNP_ID_11636557 m1A Human chr1 - 45014560 45014560 45014560 CCATCCCAATCCTCACCATGGGCACTGGTGCCAGGCCTGCCTCCCGCAACCTGGCCTTCACTTGC CCATCCCAATCCTCACCATGGGCACTGGTGCCTGGCCTGCCTCCCGCAACCTGGCCTTCACTTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45014509..45014597 26863196 MeRIP-seq:(Medium) rs36033115 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_620 GWAS_ID_13247 101471 RMVar_ID_101471 Human_SNP_ID_11636632 m1A Human chr1 + 45014827 45014827 45014827 GGTGGTTGGGCTTGACTGGACAGTGGCCCCAAAGAAAGCCCGGTAAGCCATGGAAGGGTGAGGCC GGTGGTTGGGCTTGACTGGACAGTGGCCCCAAGGAAAGCCCGGTAAGCCATGGAAGGGTGAGGCC A G UROD Ensembl:ENSG00000126088 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45014777..45015033 26863196 MeRIP-seq:(Medium) rs1222532441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356329,Human_RBP_ID_3933454,Human_RBP_ID_9319986,Human_RBP_ID_22430568,Human_RBP_ID_26386028 Human_Splice_Rec_62670,Human_Splice_Rec_62671,Human_Splice_Rec_62696,Human_Splice_Rec_62697,Human_Splice_Rec_62716,Human_Splice_Rec_62717,Human_Splice_Rec_62732,Human_Splice_Rec_62733,Human_Splice_Rec_62750,Human_Splice_Rec_62751,Human_Splice_Rec_62782,Human_Splice_Rec_62783,Human_Splice_Rec_62795,Human_Splice_Rec_62824,Human_Splice_Rec_62825,Human_Splice_Rec_62876,Human_Splice_Rec_62888,Human_Splice_Rec_62898,Human_Splice_Rec_62908,Human_Splice_Rec_62932,Human_Splice_Rec_62933,Human_Splice_Rec_62938,Human_Splice_Rec_62939,Human_Splice_Rec_62945 RMVar_hsa_circ_11232,RMVar_hsa_circ_119027,RMVar_hsa_circ_132478 101472 RMVar_ID_101472 Human_SNP_ID_11664925 m1A Human chr1 - 45139329 45139329 45139329 GAAAAGAAAGAGAAATTAGCCACCATGGTAGCAGGCGTCTGTAGTCCCAGCTAGTAAGGAGGCTG GAAAAGAAAGAGAAATTAGCCACCATGGTAGCCGGCGTCTGTAGTCCCAGCTAGTAAGGAGGCTG T G ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:45139312..45139425 26863196 MeRIP-seq:(Medium) rs987439519 Functional Loss SNV dbSNP153 33..33 33 - - - 101473 RMVar_ID_101473 Human_SNP_ID_11680662 m1A Human chr1 + 45206566 45206566 45206566 GGGCAGACGCGGGCGGCCTGCAGGGTAGCGTGAGGCGGCGCGCGGTGTCCTGGCCGCCGCGGACG GGGCAGACGCGGGCGGCCTGCAGGGTAGCGTGCGGCGGCGCGCGGTGTCCTGGCCGCCGCGGACG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:45206465..45206651 26863410 MeRIP-seq:(Medium) rs1340278934 Functional Loss SNV dbSNP153 33..33 33 - - - 101474 RMVar_ID_101474 Human_SNP_ID_11702861 m1A Human chr1 + 45303907 45303907 45303907 TGTCCGCCGGCGCCCCCTGGGATTGGGGAGAGAGGGAAGGGCTGAGGCTCACGGTTTCGGAGTAA TGTCCGCCGGCGCCCCCTGGGATTGGGGAGAGCGGGAAGGGCTGAGGCTCACGGTTTCGGAGTAA A C LINC01144,LINC01144:2,LINC01144:3,LINC01144:4,LINC01144:5 RNACentral:URS0000D59CDA,RNACentral:URS0000D5A56D,RNACentral:URS0000D5D420,RNACentral:URS0000D5C242,RNACentral:URS0000D5764C lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45303859..45303982 26863196 MeRIP-seq:(Medium) rs1416591507 Functional Loss SNV dbSNP153 33..33 33 - - - 101475 RMVar_ID_101475 Human_SNP_ID_11708415 m1A Human chr1 + 45327143 45327143 45327143 CCCCAGAAGGACAAGTCTAGGTCGCCGTCCAGAGCGCCATGGCCGCGCCCGCCCTTCGTTTGTGC CCCCAGAAGGACAAGTCTAGGTCGCCGTCCAGGGCGCCATGGCCGCGCCCGCCCTTCGTTTGTGC A G HPDL Ensembl:ENSG00000186603 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:45327098..45327300 26863196 MeRIP-seq:(Medium) rs72890563 Functional Loss SNV dbSNP153 33..33 33 - - - 101476 RMVar_ID_101476 Human_SNP_ID_11709927 m1A Human chr1 - 45331327 45331327 45331327 TTGAACCCCTTGACCCTTCCTCCAGGTTGTCCACACCTTCTCTCACATCAAGCTGACATATCAAG TTGAACCCCTTGACCCTTCCTCCAGGTTGTCCTCACCTTCTCTCACATCAAGCTGACATATCAAG T A MUTYH,AL451136.1 Ensembl:ENSG00000132781,Ensembl:ENSG00000288208 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45331278..45331665 32194978 MeRIP-seq:(Medium) rs144309934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17752401 Human_Splice_Rec_62984,Human_Splice_Rec_63018,Human_Splice_Rec_63046,Human_Splice_Rec_63074,Human_Splice_Rec_63102,Human_Splice_Rec_63130,Human_Splice_Rec_63158,Human_Splice_Rec_63186,Human_Splice_Rec_63214,Human_Splice_Rec_63242,Human_Splice_Rec_63270,Human_Splice_Rec_63298,Human_Splice_Rec_63308,Human_Splice_Rec_63336,Human_Splice_Rec_63366,Human_Splice_Rec_63378,Human_Splice_Rec_63384,Human_Splice_Rec_63392,Human_Splice_Rec_63408,Human_Splice_Rec_63436,Human_Splice_Rec_63460,Human_Splice_Rec_63488,Human_Splice_Rec_63508,Human_Splice_Rec_63754 Clinvar_Rec_621 RMVar_hsa_circ_7752,RMVar_hsa_circ_307414,RMVar_hsa_circ_132491,RMVar_hsa_circ_132492 101477 RMVar_ID_101477 Human_SNP_ID_11709928 m1A Human chr1 - 45331327 45331327 45331327 TTGAACCCCTTGACCCTTCCTCCAGGTTGTCCACACCTTCTCTCACATCAAGCTGACATATCAAG TTGAACCCCTTGACCCTTCCTCCAGGTTGTCCGCACCTTCTCTCACATCAAGCTGACATATCAAG T C MUTYH,AL451136.1 Ensembl:ENSG00000132781,Ensembl:ENSG00000288208 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45331278..45331665 32194978 MeRIP-seq:(Medium) rs144309934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17752401 Human_Splice_Rec_62984,Human_Splice_Rec_63018,Human_Splice_Rec_63046,Human_Splice_Rec_63074,Human_Splice_Rec_63102,Human_Splice_Rec_63130,Human_Splice_Rec_63158,Human_Splice_Rec_63186,Human_Splice_Rec_63214,Human_Splice_Rec_63242,Human_Splice_Rec_63270,Human_Splice_Rec_63298,Human_Splice_Rec_63308,Human_Splice_Rec_63336,Human_Splice_Rec_63366,Human_Splice_Rec_63378,Human_Splice_Rec_63384,Human_Splice_Rec_63392,Human_Splice_Rec_63408,Human_Splice_Rec_63436,Human_Splice_Rec_63460,Human_Splice_Rec_63488,Human_Splice_Rec_63508,Human_Splice_Rec_63754 Clinvar_Rec_621 RMVar_hsa_circ_7752,RMVar_hsa_circ_307414,RMVar_hsa_circ_132491,RMVar_hsa_circ_132492 101478 RMVar_ID_101478 Human_SNP_ID_11710218 m1A Human chr1 + 45331811 45331811 45331811 GACCACTCCCAGGGTCTGGTCCCAGGGCTCCGAGGGAGGCAGGCACAGGTGGCACTGTCCAGTGT GACCACTCCCAGGGTCTGGTCCCAGGGCTCCGTGGGAGGCAGGCACAGGTGGCACTGTCCAGTGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45331763..45331863 32194978 MeRIP-seq:(Medium) rs761738565 Functional Loss SNV dbSNP153 33..33 33 - - - 101479 RMVar_ID_101479 Human_SNP_ID_11710688 m1A Human chr1 + 45332674 45332674 45332674 GGGTCTCTGCTGTACGTGGCATGTGGCCCCCTAGCTCCTCTACCACCTGATTGGAGTGCAAGACT GGGTCTCTGCTGTACGTGGCATGTGGCCCCCTGGCTCCTCTACCACCTGATTGGAGTGCAAGACT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45332624..45332823 32194978 MeRIP-seq:(Medium) rs757414131 Functional Loss SNV dbSNP153 33..33 33 - - - 101480 RMVar_ID_101480 Human_SNP_ID_11713049 m1A Human chr1 + 45340519 45340519 45340519 TGGGAGCATGGGGCTGATGGAGGCATGGCGGGAGATGTAGTCTGGAGCTCATAACGGTTAGTAGT TGGGAGCATGGGGCTGATGGAGGCATGGCGGGGGATGTAGTCTGGAGCTCATAACGGTTAGTAGT A G TOE1 Ensembl:ENSG00000132773 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45340516..45341197 32194978 MeRIP-seq:(Medium) rs1012424747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_63797 101481 RMVar_ID_101481 Human_SNP_ID_11713824 m1A Human chr1 + 45342916 45342916 45342916 ACCTTACCCTGGAGTTCTGCAACTATCCTTCCAGCATGAGGGACCATATTGATTACCGCTGCTGC ACCTTACCCTGGAGTTCTGCAACTATCCTTCCGGCATGAGGGACCATATTGATTACCGCTGCTGC A G TOE1 Ensembl:ENSG00000132773 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45342848..45342949 32194978 MeRIP-seq:(Medium) rs561721650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17752409 Human_Splice_Rec_63782,Human_Splice_Rec_63783,Human_Splice_Rec_63809 101482 RMVar_ID_101482 Human_SNP_ID_11713959 m1A Human chr1 - 45343224 45343224 45343224 CCTTAGCTTCCCCAGAGGTCTGTGTCCCCGGTAGGTTCAATAAAGCCCTCTTCCGTTTTTCCCTA CCTTAGCTTCCCCAGAGGTCTGTGTCCCCGGTGGGTTCAATAAAGCCCTCTTCCGTTTTTCCCTA T C AL451136.1 Ensembl:ENSG00000288208 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45343177..45343626 32194978 MeRIP-seq:(Medium) rs1045334636 Functional Loss SNV dbSNP153 33..33 33 - - - 101483 RMVar_ID_101483 Human_SNP_ID_11751043 m1A Human chr1 + 45500375 45500375 45500375 AAGTCGCAGAGCTGAAGCAGAAGATCGAGGACACGCTATGTCCTTTTGGCTTCGAGGTTTACCCC AAGTCGCAGAGCTGAAGCAGAAGATCGAGGACGCGCTATGTCCTTTTGGCTTCGAGGTTTACCCC A G MMACHC Ensembl:ENSG00000132763 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45500332..45500417 26863196 MeRIP-seq:(Medium) rs1352943462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_63943,Human_Splice_Rec_63949 101484 RMVar_ID_101484 Human_SNP_ID_11752717 m1A Human chr1 - 45507449 45507449 45507449 GCTCTGCAAGAAGGGCTTGAGGGCCCGGTCAAACATGGCAGGCGTGCTGAGTACCAGGAAGGCCA GCTCTGCAAGAAGGGCTTGAGGGCCCGGTCAAGCATGGCAGGCGTGCTGAGTACCAGGAAGGCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45507399..45507466 26863196 MeRIP-seq:(Medium) rs778133848 Functional Loss SNV dbSNP153 33..33 33 - - - 101485 RMVar_ID_101485 Human_SNP_ID_11753596 m1A Human chr1 + 45509437 45509436 45509438 CCTTCAAATGAGTTTTTTTTTTTTTTTTAGACAGAGTCTTACTCTGTCACCTAGGCTGGAGTGCA CCTTCAAATGAGTTTTTTTTTTTTTTTTAGAC__AGTCTTACTCTGTCACCTAGGCTGGAGTGCA CAG C MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs750345461 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23149710,Human_RBP_ID_26380790 Human_Splice_Rec_63955 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 101486 RMVar_ID_101486 Human_SNP_ID_11753599 m1A Human chr1 + 45509437 45509437 45509437 CCTTCAAATGAGTTTTTTTTTTTTTTTTAGACAGAGTCTTACTCTGTCACCTAGGCTGGAGTGCA CCTTCAAATGAGTTTTTTTTTTTTTTTTAGACCGAGTCTTACTCTGTCACCTAGGCTGGAGTGCA A C MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1403162066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23149710,Human_RBP_ID_26380790 Human_Splice_Rec_63955 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 101487 RMVar_ID_101487 Human_SNP_ID_11755060 m1A Human chr1 - 45514560 45514560 45514560 TGTAAATGACCTCCCTGTTGGCCGCTCTGTGGATGAGACTTTGAGACTAGTTCAGGCCTTCCAGT TGTAAATGACCTCCCTGTTGGCCGCTCTGTGGTTGAGACTTTGAGACTAGTTCAGGCCTTCCAGT T A PRDX1 Ensembl:ENSG00000117450 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45514464..45514671 26863196 MeRIP-seq:(Medium) rs972326149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356422,Human_RBP_ID_742231,Human_RBP_ID_801959,Human_RBP_ID_1432140,Human_RBP_ID_1748866,Human_RBP_ID_3314537,Human_RBP_ID_4096724,Human_RBP_ID_5162276,Human_RBP_ID_5830531,Human_RBP_ID_8240876,Human_RBP_ID_8312702,Human_RBP_ID_8754973,Human_RBP_ID_8970732,Human_RBP_ID_11005766,Human_RBP_ID_18576211,Human_RBP_ID_21880024,Human_RBP_ID_22427228,Human_RBP_ID_22749141,Human_RBP_ID_22785217,Human_RBP_ID_22864741,Human_RBP_ID_23398323,Human_RBP_ID_26380819,Human_RBP_ID_26865682 Human_Splice_Rec_63962,Human_Splice_Rec_63963,Human_Splice_Rec_63968,Human_Splice_Rec_63969,Human_Splice_Rec_63978,Human_Splice_Rec_63979,Human_Splice_Rec_63988,Human_Splice_Rec_63996 RMVar_hsa_circ_89722,RMVar_hsa_circ_321166,RMVar_hsa_circ_344390,RMVar_hsa_circ_132504 101488 RMVar_ID_101488 Human_SNP_ID_11755062 m1A Human chr1 + 45514574 45514562 45514574 ACTAGTCTCAAAGTCTCATCCACAGAGCGGCCAACAGGGAGGTCATTTACAGTGATCTGCCGAAG ACTAGTCTCAAAGTCTCATCC____________ACAGGGAGGTCATTTACAGTGATCTGCCGAAG CACAGAGCGGCCA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45511051..45521686 32194978 MeRIP-seq:(Medium) rs763987742 Functional Loss DEL dbSNP153 22..33 33 - - - 101489 RMVar_ID_101489 Human_SNP_ID_11757605 m1A Human chr1 - 45522828 45522828 45522828 AGGCGGGAGAATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTAAGCCAACACCGTGCCACTGCAC AGGCGGGAGAATCGCTTGAGCCCGGGAGGTGGTGGTTGCAGTAAGCCAACACCGTGCCACTGCAC T A PRDX1 Ensembl:ENSG00000117450 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:45522729..45522875;chr1:45522732..45523008;chr1:45522706..45522875;chr1:45522724..45522900 26863196 MeRIP-seq:(Medium) rs1204907566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_63989 101490 RMVar_ID_101490 Human_SNP_ID_11764939 m1A Human chr1 + 45551016 45551016 45551016 GCGAAGGCGGTCCACCCTGCGCGTGATCCTTTATGCCCGGCCCCTGCCCCTCCCTCCGGGTGGAA GCGAAGGCGGTCCACCCTGCGCGTGATCCTTTGTGCCCGGCCCCTGCCCCTCCCTCCGGGTGGAA A G AKR1A1 Ensembl:ENSG00000117448 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:45550860..45551019 26863196 MeRIP-seq:(Medium) rs546869412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742215,Human_RBP_ID_4096753,Human_RBP_ID_24701729 Human_Splice_Rec_64020,Human_Splice_Rec_64038 Human_miRNA_ID_873134,Human_miRNA_ID_1230945,Human_miRNA_ID_2389249,Human_miRNA_ID_2590474,Human_miRNA_ID_2688464 RMVar_hsa_circ_127140,RMVar_hsa_circ_132506 101491 RMVar_ID_101491 Human_SNP_ID_11764940 m1A Human chr1 + 45551016 45551016 45551016 GCGAAGGCGGTCCACCCTGCGCGTGATCCTTTATGCCCGGCCCCTGCCCCTCCCTCCGGGTGGAA GCGAAGGCGGTCCACCCTGCGCGTGATCCTTTTTGCCCGGCCCCTGCCCCTCCCTCCGGGTGGAA A T AKR1A1 Ensembl:ENSG00000117448 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:45550860..45551019 26863196 MeRIP-seq:(Medium) rs546869412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_742215,Human_RBP_ID_4096753,Human_RBP_ID_24701729 Human_Splice_Rec_64020,Human_Splice_Rec_64038 Human_miRNA_ID_873134,Human_miRNA_ID_1230945,Human_miRNA_ID_2389249,Human_miRNA_ID_2590474,Human_miRNA_ID_2688464 RMVar_hsa_circ_127140,RMVar_hsa_circ_132506 101492 RMVar_ID_101492 Human_SNP_ID_11767615 m1A Human chr1 - 45561875 45561875 45561875 AGTTTCTTTTTTCTTCCCCCATCCCTCACCTGACCAGGCTCACTCTTCCAGGTACCCAGACCAAT AGTTTCTTTTTTCTTCCCCCATCCCTCACCTGCCCAGGCTCACTCTTCCAGGTACCCAGACCAAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45561736..45561930 26863196 MeRIP-seq:(Medium) rs1430666313 Functional Loss SNV dbSNP153 33..33 33 - - - 101493 RMVar_ID_101493 Human_SNP_ID_11768867 m1A Human chr1 + 45566882 45566882 45566882 GCCCTGCCCCCTGCACTAGGCGGTGCCTCGGGAGGAGCTGTTTGTGACATCCAAGCTGTGGAACA GCCCTGCCCCCTGCACTAGGCGGTGCCTCGGGTGGAGCTGTTTGTGACATCCAAGCTGTGGAACA A T AKR1A1 Ensembl:ENSG00000117448 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs780394729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3933459,Human_RBP_ID_4055847,Human_RBP_ID_17752484,Human_RBP_ID_18965443,Human_RBP_ID_22427236,Human_RBP_ID_22633640,Human_RBP_ID_22871284,Human_RBP_ID_23205158,Human_RBP_ID_24359903 Human_Splice_Rec_64008,Human_Splice_Rec_64026,Human_Splice_Rec_64046,Human_Splice_Rec_64052,Human_Splice_Rec_64056,Human_Splice_Rec_64066,Human_Splice_Rec_64072,Human_Splice_Rec_64088 RMVar_hsa_circ_81232,RMVar_hsa_circ_99348,RMVar_hsa_circ_77432,RMVar_hsa_circ_132510,RMVar_hsa_circ_132509,RMVar_hsa_circ_82270,RMVar_hsa_circ_274116,RMVar_hsa_circ_113240,RMVar_hsa_circ_269955,RMVar_hsa_circ_105747,RMVar_hsa_circ_132511,RMVar_hsa_circ_132513,RMVar_hsa_circ_132514,RMVar_hsa_circ_132512,RMVar_hsa_circ_117148,RMVar_hsa_circ_132516,RMVar_hsa_circ_132517 101494 RMVar_ID_101494 Human_SNP_ID_11769607 m1A Human chr1 - 45569214 45569214 45569214 GGCTGATACATCCTCACCGTAAGCATAGGCACAATATATCTCCAATTTTTGTTCAGGGCATTTAG GGCTGATACATCCTCACCGTAAGCATAGGCACCATATATCTCCAATTTTTGTTCAGGGCATTTAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45568926..45569950 32194978 MeRIP-seq:(Medium) rs751125273 Functional Loss SNV dbSNP153 33..33 33 - - - 101495 RMVar_ID_101495 Human_SNP_ID_11773432 m1A Human chr1 + 45584157 45584157 45584157 GGTTCGCCACCTCAGGGGAACGATGGCCATGGAGTCCACAGCCACTGCCGCCGTCGCCGCGGAGC GGTTCGCCACCTCAGGGGAACGATGGCCATGGTGTCCACAGCCACTGCCGCCGTCGCCGCGGAGC A T NASP Ensembl:ENSG00000132780 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:45584057..45584160 26863410 MeRIP-seq:(Medium) rs1421489848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19866,Human_RBP_ID_221902,Human_RBP_ID_356467,Human_RBP_ID_4055906,Human_RBP_ID_5458515,Human_RBP_ID_9318915,Human_RBP_ID_9356247,Human_RBP_ID_18576246,Human_RBP_ID_22430597,Human_RBP_ID_24358799,Human_RBP_ID_26865698 Human_Splice_Rec_64124,Human_Splice_Rec_64125,Human_Splice_Rec_64141,Human_Splice_Rec_64165,Human_Splice_Rec_64183,Human_Splice_Rec_64191,Human_Splice_Rec_64219,Human_Splice_Rec_64229,Human_Splice_Rec_64241,Human_Splice_Rec_64247,Human_Splice_Rec_64257,Human_Splice_Rec_64269,Human_Splice_Rec_64275,Human_Splice_Rec_64285,Human_Splice_Rec_64307,Human_Splice_Rec_64321,Human_Splice_Rec_64331,Human_Splice_Rec_64339,Human_Splice_Rec_64363,Human_Splice_Rec_64367 Human_miRNA_ID_2456115,Human_miRNA_ID_2461024,Human_miRNA_ID_2633681,Human_miRNA_ID_2636368 RMVar_hsa_circ_86006,RMVar_hsa_circ_348603,RMVar_hsa_circ_132524 101496 RMVar_ID_101496 Human_SNP_ID_11773440 m1A Human chr1 - 45584178 45584172 45584178 CTTACTTGTCGGCAGAAACCAGCTCCGCGGCGACGGCGGCAGTGGCTGTGGACTCCATGGCCATC CTTACTTGTCGGCAGAAACCAGCTCCGCGGCG______GCAGTGGCTGTGGACTCCATGGCCATC CCGCCGT C lnc-CCDC17-5-002 RNACentral:URS00008BBDA2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45584051..45584240 26863196 MeRIP-seq:(Medium) rs996446932 Functional Loss DEL dbSNP153 33..38 33 - - - 101497 RMVar_ID_101497 Human_SNP_ID_11776033 m1A Human chr1 - 45591205 45591205 45591205 GGAACATCTTCAATTCTGTAATAAAAAATTAAAGGGGAAAAAATGTAAAACTGGAGGCAATTATT GGAACATCTTCAATTCTGTAATAAAAAATTAAGGGGGAAAAAATGTAAAACTGGAGGCAATTATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:45591201..45591250 26863196 MeRIP-seq:(Medium) rs1235803735 Functional Loss SNV dbSNP153 33..33 33 - - - 101498 RMVar_ID_101498 Human_SNP_ID_11779127 m1A Human chr1 + 45602313 45602313 45602313 AACTATTGGGTTTAGGACAGAAACATCTGGTGATGGGGGATATTCCAGCAGCTGTCAATGCATTC AACTATTGGGTTTAGGACAGAAACATCTGGTGGTGGGGGATATTCCAGCAGCTGTCAATGCATTC A G NASP Ensembl:ENSG00000132780 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45602265..45607519 32194978 MeRIP-seq:(Medium) rs777422030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19868,Human_RBP_ID_978645,Human_RBP_ID_1748908,Human_RBP_ID_3314590,Human_RBP_ID_5830745,Human_RBP_ID_11006623,Human_RBP_ID_17678065,Human_RBP_ID_17752508,Human_RBP_ID_18576253,Human_RBP_ID_18968289,Human_RBP_ID_23398468,Human_RBP_ID_24359908 Human_Splice_Rec_64128,Human_Splice_Rec_64129,Human_Splice_Rec_64170,Human_Splice_Rec_64171,Human_Splice_Rec_64186,Human_Splice_Rec_64187,Human_Splice_Rec_64194,Human_Splice_Rec_64195,Human_Splice_Rec_64224,Human_Splice_Rec_64225,Human_Splice_Rec_64246,Human_Splice_Rec_64254,Human_Splice_Rec_64255,Human_Splice_Rec_64262,Human_Splice_Rec_64263,Human_Splice_Rec_64276,Human_Splice_Rec_64277,Human_Splice_Rec_64290,Human_Splice_Rec_64291,Human_Splice_Rec_64324,Human_Splice_Rec_64325,Human_Splice_Rec_64342,Human_Splice_Rec_64343,Human_Splice_Rec_64370,Human_Splice_Rec_64371 RMVar_hsa_circ_29575,RMVar_hsa_circ_91567,RMVar_hsa_circ_322904,RMVar_hsa_circ_317051,RMVar_hsa_circ_55180,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_132526,RMVar_hsa_circ_290481,RMVar_hsa_circ_345254,RMVar_hsa_circ_347180,RMVar_hsa_circ_114940,RMVar_hsa_circ_132527,RMVar_hsa_circ_132528,RMVar_hsa_circ_312014,RMVar_hsa_circ_314168,RMVar_hsa_circ_369014,RMVar_hsa_circ_39278,RMVar_hsa_circ_132529,RMVar_hsa_circ_2484 101499 RMVar_ID_101499 Human_SNP_ID_11779128 m1A Human chr1 + 45602313 45602313 45602313 AACTATTGGGTTTAGGACAGAAACATCTGGTGATGGGGGATATTCCAGCAGCTGTCAATGCATTC AACTATTGGGTTTAGGACAGAAACATCTGGTGTTGGGGGATATTCCAGCAGCTGTCAATGCATTC A T NASP Ensembl:ENSG00000132780 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45602265..45607519 32194978 MeRIP-seq:(Medium) rs777422030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19868,Human_RBP_ID_978645,Human_RBP_ID_1748908,Human_RBP_ID_3314590,Human_RBP_ID_5830745,Human_RBP_ID_11006623,Human_RBP_ID_17678065,Human_RBP_ID_17752508,Human_RBP_ID_18576253,Human_RBP_ID_18968289,Human_RBP_ID_23398468,Human_RBP_ID_24359908 Human_Splice_Rec_64128,Human_Splice_Rec_64129,Human_Splice_Rec_64170,Human_Splice_Rec_64171,Human_Splice_Rec_64186,Human_Splice_Rec_64187,Human_Splice_Rec_64194,Human_Splice_Rec_64195,Human_Splice_Rec_64224,Human_Splice_Rec_64225,Human_Splice_Rec_64246,Human_Splice_Rec_64254,Human_Splice_Rec_64255,Human_Splice_Rec_64262,Human_Splice_Rec_64263,Human_Splice_Rec_64276,Human_Splice_Rec_64277,Human_Splice_Rec_64290,Human_Splice_Rec_64291,Human_Splice_Rec_64324,Human_Splice_Rec_64325,Human_Splice_Rec_64342,Human_Splice_Rec_64343,Human_Splice_Rec_64370,Human_Splice_Rec_64371 RMVar_hsa_circ_29575,RMVar_hsa_circ_91567,RMVar_hsa_circ_322904,RMVar_hsa_circ_317051,RMVar_hsa_circ_55180,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_132526,RMVar_hsa_circ_290481,RMVar_hsa_circ_345254,RMVar_hsa_circ_347180,RMVar_hsa_circ_114940,RMVar_hsa_circ_132527,RMVar_hsa_circ_132528,RMVar_hsa_circ_312014,RMVar_hsa_circ_314168,RMVar_hsa_circ_369014,RMVar_hsa_circ_39278,RMVar_hsa_circ_132529,RMVar_hsa_circ_2484 101500 RMVar_ID_101500 Human_SNP_ID_11780602 m1A Human chr1 + 45607703 45607703 45607703 TGCAGAGAAAAAGGAGGTCAGGAGAAGCAGGGAGAGGTAATTGTGAGCATAGAGGAGAAGCCAAA TGCAGAGAAAAAGGAGGTCAGGAGAAGCAGGGTGAGGTAATTGTGAGCATAGAGGAGAAGCCAAA A T NASP Ensembl:ENSG00000132780 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:45607604..45607867;chr1:45606679..45607900 26863196 MeRIP-seq:(Medium) rs1216489451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19875,Human_RBP_ID_221907,Human_RBP_ID_4055949,Human_RBP_ID_5830795,Human_RBP_ID_11006881,Human_RBP_ID_18576273,Human_RBP_ID_22871782,Human_RBP_ID_23117550,Human_RBP_ID_24541467,Human_RBP_ID_24550364,Human_RBP_ID_26311168,Human_RBP_ID_27797962 RMVar_hsa_circ_91567,RMVar_hsa_circ_55180,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_114940,RMVar_hsa_circ_132528,RMVar_hsa_circ_369014,RMVar_hsa_circ_39278,RMVar_hsa_circ_54989,RMVar_hsa_circ_81349,RMVar_hsa_circ_2484,RMVar_hsa_circ_68979,RMVar_hsa_circ_132531,RMVar_hsa_circ_77135,RMVar_hsa_circ_132532 101501 RMVar_ID_101501 Human_SNP_ID_11780607 m1A Human chr1 - 45607714 45607714 45607714 CTGAAACTTCTTTTGGCTTCTCCTCTATGCTCACAATTACCTCTCCCTGCTTCTCCTGACCTCCT CTGAAACTTCTTTTGGCTTCTCCTCTATGCTCCCAATTACCTCTCCCTGCTTCTCCTGACCTCCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:45607651..45607900 26863196 MeRIP-seq:(Medium) rs1019613935 Functional Loss SNV dbSNP153 33..33 33 - - - 101502 RMVar_ID_101502 Human_SNP_ID_11780758 m1A Human chr1 - 45608061 45608056 45608062 TGGTTCAATAGGAGTCTGATCTCCTACAACTGACGGTCCATTGACTGCACCATCCTTAGGGAGAA TGGTTCAATAGGAGTCTGATCTCCTACAACT______CCATTGACTGCACCATCCTTAGGGAGAA GACCGTC G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45607717..45608066 32194978 MeRIP-seq:(Medium) rs1020550258 Functional Loss DEL dbSNP153 32..37 33 - - - 101503 RMVar_ID_101503 Human_SNP_ID_11780801 m1A Human chr1 - 45608168 45608168 45608168 TCTACAGACAGCTTAGTCTCCTCCTGACTAGGAACCAGCTTTGCCCTGACCTTCTCCTCTAGTCC TCTACAGACAGCTTAGTCTCCTCCTGACTAGGGACCAGCTTTGCCCTGACCTTCTCCTCTAGTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:45608164..45608265 26863196 MeRIP-seq:(Medium) rs372580197 Functional Loss SNV dbSNP153 33..33 33 - - - 101504 RMVar_ID_101504 Human_SNP_ID_11780857 m1A Human chr1 + 45608306 45608305 45608307 AAAGTTCAGATAGCTGCTAATGAAGAGACACAAGAGAGAGAAGAACAGATGAAAGAGGGTGAAGG AAAGTTCAGATAGCTGCTAATGAAGAGACACA__AGAGAGAAGAACAGATGAAAGAGGGTGAAGG AAG A NASP Ensembl:ENSG00000132780 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45608164..45608315 32194978 MeRIP-seq:(Medium) rs763614095 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_19879,Human_RBP_ID_858762,Human_RBP_ID_5830804,Human_RBP_ID_9356260,Human_RBP_ID_11006909,Human_RBP_ID_22350452,Human_RBP_ID_23398494,Human_RBP_ID_24541111,Human_RBP_ID_26311171,Human_RBP_ID_26865744,Human_RBP_ID_27800267 Human_Splice_Rec_64147,Human_Splice_Rec_64201,Human_Splice_Rec_64297 Human_miRNA_ID_2929436,Human_miRNA_ID_3115510 RMVar_hsa_circ_91567,RMVar_hsa_circ_55180,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_114940,RMVar_hsa_circ_132528,RMVar_hsa_circ_369014,RMVar_hsa_circ_39278,RMVar_hsa_circ_54989,RMVar_hsa_circ_81349,RMVar_hsa_circ_2484,RMVar_hsa_circ_68979,RMVar_hsa_circ_132531,RMVar_hsa_circ_77135,RMVar_hsa_circ_132532 101505 RMVar_ID_101505 Human_SNP_ID_11781516 m1A Human chr1 - 45610738 45610737 45610739 CACCCCAGCTGGGCATGGTGATACACACCCATAGTCTCAGCTGCCTGAGAGACTGAGGGAGGAAG CACCCCAGCTGGGCATGGTGATACACACCCA__GTCTCAGCTGCCTGAGAGACTGAGGGAGGAAG CTA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45610717..45610818 32194978 MeRIP-seq:(Medium) rs1176084682 Functional Loss DEL dbSNP153 32..33 33 - - - 101506 RMVar_ID_101506 Human_SNP_ID_11781517 m1A Human chr1 - 45610738 45610738 45610738 CACCCCAGCTGGGCATGGTGATACACACCCATAGTCTCAGCTGCCTGAGAGACTGAGGGAGGAAG CACCCCAGCTGGGCATGGTGATACACACCCATTGTCTCAGCTGCCTGAGAGACTGAGGGAGGAAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45610717..45610818 32194978 MeRIP-seq:(Medium) rs1442096468 Functional Loss SNV dbSNP153 33..33 33 - - - 101507 RMVar_ID_101507 Human_SNP_ID_11782540 m1A Human chr1 + 45614187 45614187 45614187 GGATTTAGCAAAGATCATTTTTAAAAGGTAAAACTCTTGGTGCTTCTAGGCTTGGGTTGGGAGTT GGATTTAGCAAAGATCATTTTTAAAAGGTAAAGCTCTTGGTGCTTCTAGGCTTGGGTTGGGAGTT A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:45614186..45614300 26863196 MeRIP-seq:(Medium) rs1169686450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11007231,Human_RBP_ID_22636956 Human_Splice_Rec_64136,Human_Splice_Rec_64150,Human_Splice_Rec_64178,Human_Splice_Rec_64204,Human_Splice_Rec_64234,Human_Splice_Rec_64284,Human_Splice_Rec_64300,Human_Splice_Rec_64314,Human_Splice_Rec_64348,Human_Splice_Rec_64378,Human_Splice_Rec_64396,Human_Splice_Rec_64412,Human_Splice_Rec_64428 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_114940,RMVar_hsa_circ_132528,RMVar_hsa_circ_369014,RMVar_hsa_circ_40562,RMVar_hsa_circ_81349,RMVar_hsa_circ_2484,RMVar_hsa_circ_68979,RMVar_hsa_circ_67882,RMVar_hsa_circ_132531,RMVar_hsa_circ_277060,RMVar_hsa_circ_132534 101508 RMVar_ID_101508 Human_SNP_ID_11782944 m1A Human chr1 + 45615387 45615387 45615387 AAGAAAGAAATTGAGGAACTAAAGGAACTGCTACCCGAAATTAGAGAGAAGATAGAAGATGCAAA AAGAAAGAAATTGAGGAACTAAAGGAACTGCTGCCCGAAATTAGAGAGAAGATAGAAGATGCAAA A G NASP Ensembl:ENSG00000132780 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45615336..45615425 26863196 MeRIP-seq:(Medium) rs1007051816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19882,Human_RBP_ID_272946,Human_RBP_ID_356491,Human_RBP_ID_803004,Human_RBP_ID_858769,Human_RBP_ID_1748989,Human_RBP_ID_2150017,Human_RBP_ID_3314635,Human_RBP_ID_5518986,Human_RBP_ID_5537913,Human_RBP_ID_5830914,Human_RBP_ID_8749798,Human_RBP_ID_9356272,Human_RBP_ID_11007261,Human_RBP_ID_18523277,Human_RBP_ID_22488334,Human_RBP_ID_22785238,Human_RBP_ID_22864844,Human_RBP_ID_24541114,Human_RBP_ID_26309747,Human_RBP_ID_27797974 Human_Splice_Rec_64156,Human_Splice_Rec_64157,Human_Splice_Rec_64210,Human_Splice_Rec_64211,Human_Splice_Rec_64240,Human_Splice_Rec_64306,Human_Splice_Rec_64320,Human_Splice_Rec_64354,Human_Splice_Rec_64355,Human_Splice_Rec_64384,Human_Splice_Rec_64385,Human_Splice_Rec_64402,Human_Splice_Rec_64403,Human_Splice_Rec_64418,Human_Splice_Rec_64419,Human_Splice_Rec_64434,Human_Splice_Rec_64435,Human_Splice_Rec_64444,Human_Splice_Rec_64446,Human_Splice_Rec_64447 Human_miRNA_ID_3115511 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_114940,RMVar_hsa_circ_132528,RMVar_hsa_circ_81349,RMVar_hsa_circ_2484,RMVar_hsa_circ_67882,RMVar_hsa_circ_132531,RMVar_hsa_circ_277060,RMVar_hsa_circ_132535,RMVar_hsa_circ_41527,RMVar_hsa_circ_132534,RMVar_hsa_circ_296587 101509 RMVar_ID_101509 Human_SNP_ID_11783565 m1A Human chr1 + 45617512 45617512 45617512 GAGTCCCCGGAAAGATGATGCAAAGAAAGCCAAACAAGAGCCGGAGGTGAACGGAGGCAGTGGGG GAGTCCCCGGAAAGATGATGCAAAGAAAGCCAGACAAGAGCCGGAGGTGAACGGAGGCAGTGGGG A G NASP Ensembl:ENSG00000132780 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:45617428..45617600;chr1:45617426..45618150 26863196 MeRIP-seq:(Medium) rs1311418778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3936007,Human_RBP_ID_4096824,Human_RBP_ID_5108627,Human_RBP_ID_5537915,Human_RBP_ID_9356279,Human_RBP_ID_18158303,Human_RBP_ID_18576319,Human_RBP_ID_22144280,Human_RBP_ID_26311188,Human_RBP_ID_27797977 Human_Splice_Rec_64162,Human_Splice_Rec_64163,Human_Splice_Rec_64216,Human_Splice_Rec_64217,Human_Splice_Rec_64360,Human_Splice_Rec_64361,Human_Splice_Rec_64390,Human_Splice_Rec_64391,Human_Splice_Rec_64408,Human_Splice_Rec_64409,Human_Splice_Rec_64424,Human_Splice_Rec_64425,Human_Splice_Rec_64440,Human_Splice_Rec_64441,Human_Splice_Rec_64453 Human_miRNA_ID_2014559 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_336131 101510 RMVar_ID_101510 Human_SNP_ID_11783566 m1A Human chr1 + 45617516 45617514 45617516 CCCCGGAAAGATGATGCAAAGAAAGCCAAACAAGAGCCGGAGGTGAACGGAGGCAGTGGGGATGC CCCCGGAAAGATGATGCAAAGAAAGCCAAAC__GAGCCGGAGGTGAACGGAGGCAGTGGGGATGC CAA C NASP Ensembl:ENSG00000132780 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45617466..45617627 26863196 MeRIP-seq:(Medium) rs1485794709 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3936007,Human_RBP_ID_4096824,Human_RBP_ID_5108627,Human_RBP_ID_5537915,Human_RBP_ID_5830927,Human_RBP_ID_9356279,Human_RBP_ID_11007302,Human_RBP_ID_17668188,Human_RBP_ID_18158303,Human_RBP_ID_26311188,Human_RBP_ID_27797977 Human_Splice_Rec_64162,Human_Splice_Rec_64163,Human_Splice_Rec_64216,Human_Splice_Rec_64217,Human_Splice_Rec_64360,Human_Splice_Rec_64361,Human_Splice_Rec_64390,Human_Splice_Rec_64391,Human_Splice_Rec_64408,Human_Splice_Rec_64409,Human_Splice_Rec_64424,Human_Splice_Rec_64425,Human_Splice_Rec_64440,Human_Splice_Rec_64441,Human_Splice_Rec_64453 Human_miRNA_ID_2014559 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_336131 101511 RMVar_ID_101511 Human_SNP_ID_11783567 m1A Human chr1 + 45617516 45617516 45617516 CCCCGGAAAGATGATGCAAAGAAAGCCAAACAAGAGCCGGAGGTGAACGGAGGCAGTGGGGATGC CCCCGGAAAGATGATGCAAAGAAAGCCAAACAGGAGCCGGAGGTGAACGGAGGCAGTGGGGATGC A G NASP Ensembl:ENSG00000132780 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45617466..45617627 26863196 MeRIP-seq:(Medium) rs888272493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3936007,Human_RBP_ID_4096824,Human_RBP_ID_5108627,Human_RBP_ID_5537915,Human_RBP_ID_5830927,Human_RBP_ID_9356279,Human_RBP_ID_11007302,Human_RBP_ID_17668188,Human_RBP_ID_18158303,Human_RBP_ID_26311188,Human_RBP_ID_27797977 Human_Splice_Rec_64162,Human_Splice_Rec_64163,Human_Splice_Rec_64216,Human_Splice_Rec_64217,Human_Splice_Rec_64360,Human_Splice_Rec_64361,Human_Splice_Rec_64390,Human_Splice_Rec_64391,Human_Splice_Rec_64408,Human_Splice_Rec_64409,Human_Splice_Rec_64424,Human_Splice_Rec_64425,Human_Splice_Rec_64440,Human_Splice_Rec_64441,Human_Splice_Rec_64453 Human_miRNA_ID_2014559 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_336131 101512 RMVar_ID_101512 Human_SNP_ID_11783582 m1A Human chr1 + 45617545 45617545 45617545 ACAAGAGCCGGAGGTGAACGGAGGCAGTGGGGATGCTGTCCCCAGTGGAAATGAAGTTTCGGAAA ACAAGAGCCGGAGGTGAACGGAGGCAGTGGGGGTGCTGTCCCCAGTGGAAATGAAGTTTCGGAAA A G NASP Ensembl:ENSG00000132780 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:45617501..45617651 26863196 MeRIP-seq:(Medium) rs141540892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221923,Human_RBP_ID_356498,Human_RBP_ID_742777,Human_RBP_ID_3314640,Human_RBP_ID_3936007,Human_RBP_ID_4096824,Human_RBP_ID_5108627,Human_RBP_ID_5830927,Human_RBP_ID_9356279,Human_RBP_ID_11007302,Human_RBP_ID_17668189,Human_RBP_ID_18158303,Human_RBP_ID_26311188,Human_RBP_ID_27797977 Human_Splice_Rec_64162,Human_Splice_Rec_64163,Human_Splice_Rec_64216,Human_Splice_Rec_64217,Human_Splice_Rec_64360,Human_Splice_Rec_64361,Human_Splice_Rec_64390,Human_Splice_Rec_64391,Human_Splice_Rec_64408,Human_Splice_Rec_64409,Human_Splice_Rec_64424,Human_Splice_Rec_64425,Human_Splice_Rec_64440,Human_Splice_Rec_64441,Human_Splice_Rec_64453 Human_miRNA_ID_2421132,Human_miRNA_ID_2967021 RMVar_hsa_circ_91567,RMVar_hsa_circ_132525,RMVar_hsa_circ_336131 101513 RMVar_ID_101513 Human_SNP_ID_11787676 m1A Human chr1 - 45627957 45627957 45627957 TGGGGCGATGCACAGGTAGGAGCTGGCAGTGCAGGGAAGAGGAGACACTGGTCTGCAGCAACAGC TGGGGCGATGCACAGGTAGGAGCTGGCAGTGCTGGGAAGAGGAGACACTGGTCTGCAGCAACAGC T A GPBP1L1 Ensembl:ENSG00000159592 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45627852..45628202 32194978 MeRIP-seq:(Medium) rs1460986818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356539,Human_RBP_ID_803768,Human_RBP_ID_5830977,Human_RBP_ID_11007447,Human_RBP_ID_17338964,Human_RBP_ID_23398590 Human_miRNA_ID_2174187,Human_miRNA_ID_2177631 RMVar_hsa_circ_85596,RMVar_hsa_circ_122140,RMVar_hsa_circ_119706,RMVar_hsa_circ_132538,RMVar_hsa_circ_132539,RMVar_hsa_circ_132540 101514 RMVar_ID_101514 Human_SNP_ID_11787827 m1A Human chr1 + 45628348 45628348 45628348 AAACTCTGCTTTGCAAGTGCTTCTCCAAGGGGAGAACAGACTGGAACTGCGGCTCTGCAAGAAGC AAACTCTGCTTTGCAAGTGCTTCTCCAAGGGGCGAACAGACTGGAACTGCGGCTCTGCAAGAAGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45628301..45629618 32194978 MeRIP-seq:(Medium) rs1439475210 Functional Loss SNV dbSNP153 33..33 33 - - - 101515 RMVar_ID_101515 Human_SNP_ID_11789418 m1A Human chr1 - 45633624 45633624 45633624 TTTGCCCAGAGTCCCTCCAGCACCACCCCTCCAATTGAGATCAGCTCCTCTCGTCTGACCAAGTT TTTGCCCAGAGTCCCTCCAGCACCACCCCTCCGATTGAGATCAGCTCCTCTCGTCTGACCAAGTT T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45633513..45633714 32194978 MeRIP-seq:(Medium) rs1455600138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743632,Human_RBP_ID_23112659 Human_Splice_Rec_64590,Human_Splice_Rec_64614,Human_Splice_Rec_64636 Human_miRNA_ID_2290823,Human_miRNA_ID_2356170,Human_miRNA_ID_3058614 RMVar_hsa_circ_1438,RMVar_hsa_circ_108446,RMVar_hsa_circ_85596,RMVar_hsa_circ_122140,RMVar_hsa_circ_119706,RMVar_hsa_circ_132538,RMVar_hsa_circ_132539,RMVar_hsa_circ_132540,RMVar_hsa_circ_132541,RMVar_hsa_circ_378761,RMVar_hsa_circ_108892,RMVar_hsa_circ_132543,RMVar_hsa_circ_77468,RMVar_hsa_circ_87077,RMVar_hsa_circ_132544,RMVar_hsa_circ_132545,RMVar_hsa_circ_288002,RMVar_hsa_circ_334747,RMVar_hsa_circ_132542,RMVar_hsa_circ_371791,RMVar_hsa_circ_324901,RMVar_hsa_circ_127980,RMVar_hsa_circ_283999,RMVar_hsa_circ_88773,RMVar_hsa_circ_274379,RMVar_hsa_circ_132547,RMVar_hsa_circ_132548,RMVar_hsa_circ_132549,RMVar_hsa_circ_363485,RMVar_hsa_circ_132546,RMVar_hsa_circ_369593,RMVar_hsa_circ_360601,RMVar_hsa_circ_132551,RMVar_hsa_circ_132552,RMVar_hsa_circ_132550 101516 RMVar_ID_101516 Human_SNP_ID_11791228 m1A Human chr1 - 45640401 45640401 45640401 CTGTTGTCTCTCCACTCTTGTACTTCACAGAAAACCCGCCTAGTGCCAAGCAACCCTCCAAGATG CTGTTGTCTCTCCACTCTTGTACTTCACAGAAGACCCGCCTAGTGCCAAGCAACCCTCCAAGATG T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45635723..45641724 32194978 MeRIP-seq:(Medium) rs763083962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3933469,Human_RBP_ID_24702342 Human_Splice_Rec_64610,Human_Splice_Rec_64632 RMVar_hsa_circ_1438,RMVar_hsa_circ_108446,RMVar_hsa_circ_85596,RMVar_hsa_circ_122140,RMVar_hsa_circ_132538,RMVar_hsa_circ_132539,RMVar_hsa_circ_132541,RMVar_hsa_circ_378761,RMVar_hsa_circ_108892,RMVar_hsa_circ_132543,RMVar_hsa_circ_87077,RMVar_hsa_circ_132544,RMVar_hsa_circ_132545,RMVar_hsa_circ_288002,RMVar_hsa_circ_334747,RMVar_hsa_circ_127980,RMVar_hsa_circ_283999,RMVar_hsa_circ_88773,RMVar_hsa_circ_132556,RMVar_hsa_circ_117168,RMVar_hsa_circ_274379,RMVar_hsa_circ_132547,RMVar_hsa_circ_132548,RMVar_hsa_circ_132549,RMVar_hsa_circ_363485,RMVar_hsa_circ_369593,RMVar_hsa_circ_360601,RMVar_hsa_circ_132551,RMVar_hsa_circ_132552,RMVar_hsa_circ_366749,RMVar_hsa_circ_132550,RMVar_hsa_circ_267289,RMVar_hsa_circ_305521,RMVar_hsa_circ_132554,RMVar_hsa_circ_41082,RMVar_hsa_circ_132553,RMVar_hsa_circ_336735,RMVar_hsa_circ_293007,RMVar_hsa_circ_299141,RMVar_hsa_circ_132557,RMVar_hsa_circ_132555 101517 RMVar_ID_101517 Human_SNP_ID_11791839 m1A Human chr1 - 45642489 45642489 45642489 ATTCATATCCCTTTTTTCCTAGCCTTCCTTGAATCCAGAAGCTGGCAAACAGCATCAGCCATGCA ATTCATATCCCTTTTTTCCTAGCCTTCCTTGAGTCCAGAAGCTGGCAAACAGCATCAGCCATGCA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45642438..45654309 32194978 MeRIP-seq:(Medium) rs369236519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854665,Human_RBP_ID_17763690,Human_RBP_ID_19034827,Human_RBP_ID_24748232,Human_RBP_ID_26388151,Human_RBP_ID_26798345 Human_Splice_Rec_64608,Human_Splice_Rec_64609,Human_Splice_Rec_64630,Human_Splice_Rec_64631,Human_Splice_Rec_64656,Human_Splice_Rec_64657 RMVar_hsa_circ_1438,RMVar_hsa_circ_108446,RMVar_hsa_circ_85596,RMVar_hsa_circ_132538,RMVar_hsa_circ_108892,RMVar_hsa_circ_132543,RMVar_hsa_circ_87077,RMVar_hsa_circ_132544,RMVar_hsa_circ_132545,RMVar_hsa_circ_334747,RMVar_hsa_circ_127980,RMVar_hsa_circ_283999,RMVar_hsa_circ_88773,RMVar_hsa_circ_132556,RMVar_hsa_circ_117168,RMVar_hsa_circ_274379,RMVar_hsa_circ_132547,RMVar_hsa_circ_132548,RMVar_hsa_circ_132549,RMVar_hsa_circ_363485,RMVar_hsa_circ_360601,RMVar_hsa_circ_132551,RMVar_hsa_circ_132552,RMVar_hsa_circ_366749,RMVar_hsa_circ_305521,RMVar_hsa_circ_132554,RMVar_hsa_circ_41082,RMVar_hsa_circ_132553,RMVar_hsa_circ_336735,RMVar_hsa_circ_293007,RMVar_hsa_circ_299141,RMVar_hsa_circ_132557,RMVar_hsa_circ_132561,RMVar_hsa_circ_85966,RMVar_hsa_circ_286972,RMVar_hsa_circ_372844,RMVar_hsa_circ_132555,RMVar_hsa_circ_300598,RMVar_hsa_circ_269433,RMVar_hsa_circ_80147,RMVar_hsa_circ_132562,RMVar_hsa_circ_132559,RMVar_hsa_circ_132560,RMVar_hsa_circ_132558 101518 RMVar_ID_101518 Human_SNP_ID_11796443 m1A Human chr1 - 45659098 45659098 45659098 AGGTTGGATGCCTCACCTTACTGAAAGGAGACACTGGACCTAAATGGCGCAGCATGATTTTGTTC AGGTTGGATGCCTCACCTTACTGAAAGGAGACGCTGGACCTAAATGGCGCAGCATGATTTTGTTC T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45659009..45660550 32194978 MeRIP-seq:(Medium) rs1340804810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356572,Human_RBP_ID_1432231,Human_RBP_ID_1749077,Human_RBP_ID_4056124,Human_RBP_ID_5414061,Human_RBP_ID_5831175,Human_RBP_ID_8312881,Human_RBP_ID_8749820,Human_RBP_ID_11008075,Human_RBP_ID_17218858,Human_RBP_ID_22870838 Human_Splice_Rec_64602,Human_Splice_Rec_64603,Human_Splice_Rec_64624,Human_Splice_Rec_64625,Human_Splice_Rec_64662 Human_miRNA_ID_2174188,Human_miRNA_ID_2174189,Human_miRNA_ID_2177632,Human_miRNA_ID_2177633 RMVar_hsa_circ_108892,RMVar_hsa_circ_87077,RMVar_hsa_circ_132544,RMVar_hsa_circ_132545,RMVar_hsa_circ_283999,RMVar_hsa_circ_88773,RMVar_hsa_circ_117168,RMVar_hsa_circ_132549,RMVar_hsa_circ_360601,RMVar_hsa_circ_305521,RMVar_hsa_circ_132553,RMVar_hsa_circ_336735,RMVar_hsa_circ_132557,RMVar_hsa_circ_132561,RMVar_hsa_circ_372844,RMVar_hsa_circ_300598,RMVar_hsa_circ_80147,RMVar_hsa_circ_132562,RMVar_hsa_circ_132560,RMVar_hsa_circ_306659,RMVar_hsa_circ_356528,RMVar_hsa_circ_269907,RMVar_hsa_circ_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564,RMVar_hsa_circ_132565 101519 RMVar_ID_101519 Human_SNP_ID_11807138 m1A Human chr1 - 45698302 45698301 45698302 ATATATTAAAGGTCTTGCATACAGTAAAAAAAATTTTTTTTTGAGATGGAATTTTGCTCTTGTTG ATATATTAAAGGTCTTGCATACAGTAAAAAAA_TTTTTTTTTGAGATGGAATTTTGCTCTTGTTG AT A IPP Ensembl:ENSG00000197429 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1557734771 Functional Loss DEL dbSNP153 33..33 33 - - - 101520 RMVar_ID_101520 Human_SNP_ID_11807139 m1A Human chr1 - 45698302 45698302 45698302 ATATATTAAAGGTCTTGCATACAGTAAAAAAAATTTTTTTTTGAGATGGAATTTTGCTCTTGTTG ATATATTAAAGGTCTTGCATACAGTAAAAAAATTTTTTTTTTGAGATGGAATTTTGCTCTTGTTG T A IPP Ensembl:ENSG00000197429 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3014243 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13248,GWAS_ID_13249,GWAS_ID_13250,GWAS_ID_13251,GWAS_ID_13252,GWAS_ID_13253,GWAS_ID_13254,GWAS_ID_13255,GWAS_ID_13256,GWAS_ID_13257,GWAS_ID_13258,GWAS_ID_13259,GWAS_ID_13260,GWAS_ID_13261,GWAS_ID_13262,GWAS_ID_13263,GWAS_ID_13264,GWAS_ID_13265,GWAS_ID_13266,GWAS_ID_13267,GWAS_ID_13268,GWAS_ID_13269,GWAS_ID_13270,GWAS_ID_13271,GWAS_ID_13272,GWAS_ID_13273,GWAS_ID_13274,GWAS_ID_13275,GWAS_ID_13276,GWAS_ID_13277,GWAS_ID_13278,GWAS_ID_13279,GWAS_ID_13280,GWAS_ID_13281,GWAS_ID_13282,GWAS_ID_13283,GWAS_ID_13284,GWAS_ID_13285,GWAS_ID_13286,GWAS_ID_13287,GWAS_ID_13288,GWAS_ID_13289,GWAS_ID_13290,GWAS_ID_13291,GWAS_ID_13292,GWAS_ID_13293,GWAS_ID_13294,GWAS_ID_13295,GWAS_ID_13296,GWAS_ID_13297,GWAS_ID_13298,GWAS_ID_13299,GWAS_ID_13300,GWAS_ID_13301,GWAS_ID_13302,GWAS_ID_13303,GWAS_ID_13304,GWAS_ID_13305,GWAS_ID_13306,GWAS_ID_13307,GWAS_ID_13308,GWAS_ID_13309,GWAS_ID_13310,GWAS_ID_13311,GWAS_ID_13312,GWAS_ID_13313,GWAS_ID_13314,GWAS_ID_13315,GWAS_ID_13316,GWAS_ID_13317,GWAS_ID_13318,GWAS_ID_13319,GWAS_ID_13320,GWAS_ID_13321,GWAS_ID_13322,GWAS_ID_13323,GWAS_ID_13324,GWAS_ID_13325,GWAS_ID_13326,GWAS_ID_13327,GWAS_ID_13328,GWAS_ID_13329,GWAS_ID_13330,GWAS_ID_13331,GWAS_ID_13332,GWAS_ID_13333,GWAS_ID_13334,GWAS_ID_13335,GWAS_ID_13336,GWAS_ID_13337,GWAS_ID_13338,GWAS_ID_13339,GWAS_ID_13340,GWAS_ID_13341,GWAS_ID_13342,GWAS_ID_13343,GWAS_ID_13344,GWAS_ID_13345,GWAS_ID_13346,GWAS_ID_13347,GWAS_ID_13348,GWAS_ID_13349,GWAS_ID_13350,GWAS_ID_13351,GWAS_ID_13352,GWAS_ID_13353,GWAS_ID_13354,GWAS_ID_13355,GWAS_ID_13356,GWAS_ID_13357,GWAS_ID_13358,GWAS_ID_13359,GWAS_ID_13360,GWAS_ID_13361,GWAS_ID_13362,GWAS_ID_13363,GWAS_ID_13364,GWAS_ID_13365,GWAS_ID_13366,GWAS_ID_13367,GWAS_ID_13368,GWAS_ID_13369,GWAS_ID_13370 101521 RMVar_ID_101521 Human_SNP_ID_11834866 m1A Human chr1 - 45803645 45803637 45803645 CCTCGCCTTCTCCCACCCAGCACACGTTGGGCAGGCCACCCGCCGCCGGCTCAGCCGCCTGCCTA CCTCGCCTTCTCCCACCCAGCACACGTTGGGC________CGCCGCCGGCTCAGCCGCCTGCCTA GGGTGGCCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45803597..45803725 26863196 MeRIP-seq:(Medium) rs1204021708 Functional Loss DEL dbSNP153 33..40 33 - - - 101522 RMVar_ID_101522 Human_SNP_ID_11834872 m1A Human chr1 - 45803645 45803645 45803645 CCTCGCCTTCTCCCACCCAGCACACGTTGGGCAGGCCACCCGCCGCCGGCTCAGCCGCCTGCCTA CCTCGCCTTCTCCCACCCAGCACACGTTGGGCCGGCCACCCGCCGCCGGCTCAGCCGCCTGCCTA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:45803597..45803725 26863196 MeRIP-seq:(Medium) rs1004206376 Functional Loss SNV dbSNP153 33..33 33 - - - 101523 RMVar_ID_101523 Human_SNP_ID_11834882 m1A Human chr1 + 45803675 45803675 45803675 CCTGCCCAACGTGTGCTGGGTGGGAGAAGGCGAGGCGTCAGCGATGCTGTCTCTTCCGTGAGGAG CCTGCCCAACGTGTGCTGGGTGGGAGAAGGCGGGGCGTCAGCGATGCTGTCTCTTCCGTGAGGAG A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:45803557..45803734;chr1:45803546..45803747 26863196 MeRIP-seq:(Medium) rs866539826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223604,Human_RBP_ID_746223,Human_RBP_ID_801572,Human_RBP_ID_4056249,Human_RBP_ID_5519829,Human_RBP_ID_18415821,Human_RBP_ID_18968308 101524 RMVar_ID_101524 Human_SNP_ID_11835013 m1A Human chr1 - 45804083 45804082 45804083 GCTTCCATTCAGGTTCACCCTCCCGGATCCCAACCCGCCCTACCTGCTCCTTGCCCTCGGGCCCC GCTTCCATTCAGGTTCACCCTCCCGGATCCCA_CCCGCCCTACCTGCTCCTTGCCCTCGGGCCCC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45804076..45804186 26863196 MeRIP-seq:(Medium) rs955768138 Functional Loss DEL dbSNP153 33..33 33 - - - 101525 RMVar_ID_101525 Human_SNP_ID_11840175 m1A Human chr1 + 45824447 45824447 45824447 CTCTTTTTCTCTTTGAAGGATGTAGTAACTGGAGTTAGTCCCCTGCTCTTCAGGAAACTCAGTAA CTCTTTTTCTCTTTGAAGGATGTAGTAACTGGTGTTAGTCCCCTGCTCTTCAGGAAACTCAGTAA A T MAST2 Ensembl:ENSG00000086015 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45804014..45824525 32194978 MeRIP-seq:(Medium) rs529635748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851531,Human_RBP_ID_18576412 Human_Splice_Rec_64726,Human_Splice_Rec_64734 RMVar_hsa_circ_132574,RMVar_hsa_circ_84369,RMVar_hsa_circ_132573,RMVar_hsa_circ_274090,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575 101526 RMVar_ID_101526 Human_SNP_ID_11892813 m1A Human chr1 + 46034701 46034692 46034701 CGGCGCAAGTCAGCAGGCAGCATCCCACTGTCACCACTGGCCCACACCCCTTCTCCCCCACCCCC CGGCGCAAGTCAGCAGGCAGCATC_________CCACTGGCCCACACCCCTTCTCCCCCACCCCC CCCACTGTCA C MAST2 Ensembl:ENSG00000086015 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:46034651..46034725 26863196 MeRIP-seq:(Medium) rs1557524889 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_18430513 RMVar_hsa_circ_113890,RMVar_hsa_circ_132591,RMVar_hsa_circ_126872,RMVar_hsa_circ_132593,RMVar_hsa_circ_80251,RMVar_hsa_circ_118089,RMVar_hsa_circ_132595,RMVar_hsa_circ_132598 101527 RMVar_ID_101527 Human_SNP_ID_11893266 m1A Human chr1 + 46035774 46035774 46035774 AGCCCAGCCTAAGAACCTGTCTCCCAGGGAGCAGGGGAAGACACAGCCACCTAGTGCCCCCAGAC AGCCCAGCCTAAGAACCTGTCTCCCAGGGAGCCGGGGAAGACACAGCCACCTAGTGCCCCCAGAC A C MAST2 Ensembl:ENSG00000086015 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46035724..46036024 32194978 MeRIP-seq:(Medium) rs764151448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8753940,Human_RBP_ID_26314163 RMVar_hsa_circ_113890,RMVar_hsa_circ_132591,RMVar_hsa_circ_126872,RMVar_hsa_circ_132593,RMVar_hsa_circ_80251,RMVar_hsa_circ_118089,RMVar_hsa_circ_132595,RMVar_hsa_circ_132598 101528 RMVar_ID_101528 Human_SNP_ID_11901614 m1A Human chr1 - 46071073 46071071 46071073 GAAGGAGGGCCTGGGATAAAGGAAGGGGACAGAGTCTGAATTTGTTCAAAGTCATTGGTGACTCT GAAGGAGGGCCTGGGATAAAGGAAGGGGACAG__TCTGAATTTGTTCAAAGTCATTGGTGACTCT ACT A PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46071069..46071160 26863196 MeRIP-seq:(Medium) rs919184099 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_313587,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603,RMVar_hsa_circ_270585,RMVar_hsa_circ_49355,RMVar_hsa_circ_73641,RMVar_hsa_circ_132605,RMVar_hsa_circ_132606,RMVar_hsa_circ_300981,RMVar_hsa_circ_349567,RMVar_hsa_circ_285279,RMVar_hsa_circ_132610,RMVar_hsa_circ_132611,RMVar_hsa_circ_132609,RMVar_hsa_circ_318105,RMVar_hsa_circ_132612 101529 RMVar_ID_101529 Human_SNP_ID_11910992 m1A Human chr1 + 46110023 46110023 46110023 CCCTAGATACACCAATACCTGCAGCTCATCCAAACACACAACTCTTTCTCATGCCTTTGCACATA CCCTAGATACACCAATACCTGCAGCTCATCCAGACACACAACTCTTTCTCATGCCTTTGCACATA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46110008..46110127 26863196 MeRIP-seq:(Medium) rs544721238 Functional Loss SNV dbSNP153 33..33 33 - - - 101530 RMVar_ID_101530 Human_SNP_ID_11911661 m1A Human chr1 + 46113041 46113041 46113041 ACTCTACTATTCATTCTCACTGCTACAATCTTAGCCTTAGGCTTTCATAACATCTTTCTTCTGTA ACTCTACTATTCATTCTCACTGCTACAATCTTTGCCTTAGGCTTTCATAACATCTTTCTTCTGTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46113039..46113148 26863196 MeRIP-seq:(Medium) rs1434742564 Functional Loss SNV dbSNP153 33..33 33 - - - 101531 RMVar_ID_101531 Human_SNP_ID_11930407 m1A Human chr1 - 46189967 46189967 46189967 TCTACTGCAGTGAGGCTGAGGTTCTGGACCACAGCAAGAACCCTTGTGAAGACTCTTTCCTGCCA TCTACTGCAGTGAGGCTGAGGTTCTGGACCACGGCAAGAACCCTTGTGAAGACTCTTTCCTGCCA T C POMGNT1 Ensembl:ENSG00000085998 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:46189917..46190145 32194978 MeRIP-seq:(Medium) rs1241070329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854682,Human_RBP_ID_1749169,Human_RBP_ID_3314936,Human_RBP_ID_18968325 Human_Splice_Rec_65180,Human_Splice_Rec_65222,Human_Splice_Rec_65264,Human_Splice_Rec_65276 RMVar_hsa_circ_79798,RMVar_hsa_circ_86725,RMVar_hsa_circ_110668,RMVar_hsa_circ_96271,RMVar_hsa_circ_132622,RMVar_hsa_circ_132623,RMVar_hsa_circ_132624,RMVar_hsa_circ_109874,RMVar_hsa_circ_132625,RMVar_hsa_circ_132626 101532 RMVar_ID_101532 Human_SNP_ID_11931532 m1A Human chr1 + 46193621 46193621 46193621 GTTATCATCTGAGGAGACACCCCCTGGGCTGAAAGCAGAGAGCGCAGCATCCTGGGGAGCCCAGG GTTATCATCTGAGGAGACACCCCCTGGGCTGATAGCAGAGAGCGCAGCATCCTGGGGAGCCCAGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46193570..46193821 32194978 MeRIP-seq:(Medium) rs760847467 Functional Loss SNV dbSNP153 33..33 33 - - - 101533 RMVar_ID_101533 Human_SNP_ID_11931906 m1A Human chr1 - 46194705 46194704 46194705 GTTGGATGAAAGTAGGCAGGGAGATGGGAAAAAGCCCCCAAACTGGTGTCTGGGCCCCCATGGCC GTTGGATGAAAGTAGGCAGGGAGATGGGAAAA_GCCCCCAAACTGGTGTCTGGGCCCCCATGGCC CT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:46194700..46194839 26863196 MeRIP-seq:(Medium) rs1466683422 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5333247,Human_RBP_ID_9411876 RMVar_hsa_circ_16992,RMVar_hsa_circ_86725,RMVar_hsa_circ_132624,RMVar_hsa_circ_60534,RMVar_hsa_circ_44354,RMVar_hsa_circ_74319,RMVar_hsa_circ_115138,RMVar_hsa_circ_104413,RMVar_hsa_circ_132628,RMVar_hsa_circ_132629 101534 RMVar_ID_101534 Human_SNP_ID_11931907 m1A Human chr1 - 46194705 46194705 46194705 GTTGGATGAAAGTAGGCAGGGAGATGGGAAAAAGCCCCCAAACTGGTGTCTGGGCCCCCATGGCC GTTGGATGAAAGTAGGCAGGGAGATGGGAAAACGCCCCCAAACTGGTGTCTGGGCCCCCATGGCC T G POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:46194700..46194839 26863196 MeRIP-seq:(Medium) rs1429752145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5333247,Human_RBP_ID_9411876 RMVar_hsa_circ_16992,RMVar_hsa_circ_86725,RMVar_hsa_circ_132624,RMVar_hsa_circ_60534,RMVar_hsa_circ_44354,RMVar_hsa_circ_74319,RMVar_hsa_circ_115138,RMVar_hsa_circ_104413,RMVar_hsa_circ_132628,RMVar_hsa_circ_132629 101535 RMVar_ID_101535 Human_SNP_ID_11933019 m1A Human chr1 - 46198406 46198406 46198406 GGGCGGGGCCGCAAGCGGCATGGAGGAGGCGGAGGCCGCGGCGAGCCGGGCCGAGCAGTGAGGGC GGGCGGGGCCGCAAGCGGCATGGAGGAGGCGGGGGCCGCGGCGAGCCGGGCCGAGCAGTGAGGGC T C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:46198221..46198450 26863196 MeRIP-seq:(Medium) rs1334987118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801565,Human_RBP_ID_4072795 Human_Splice_Rec_65185 101536 RMVar_ID_101536 Human_SNP_ID_11933103 m1A Human chr1 - 46198542 46198524 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC__________________GCCGCCCTAAGCACC CGGCGGCGGCGGCGGCGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs1047925597 Functional Loss DEL dbSNP153 33..50 33 - - - 101537 RMVar_ID_101537 Human_SNP_ID_11933109 m1A Human chr1 - 46198542 46198527 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC_______________GCCGCCGCCCTAAGCACC CGGCGGCGGCGGCGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs1009136978 Functional Loss DEL dbSNP153 33..47 33 - - - 101538 RMVar_ID_101538 Human_SNP_ID_11933115 m1A Human chr1 - 46198542 46198530 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC____________GCCGCCGCCGCCCTAAGCACC CGGCGGCGGCGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs1039007977 Functional Loss DEL dbSNP153 33..44 33 - - - 101539 RMVar_ID_101539 Human_SNP_ID_11933120 m1A Human chr1 - 46198542 46198533 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC_________GCCGCCGCCGCCGCCCTAAGCACC CGGCGGCGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs966546165 Functional Loss DEL dbSNP153 33..41 33 - - - 101540 RMVar_ID_101540 Human_SNP_ID_11933126 m1A Human chr1 - 46198542 46198536 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC______GCCGCCGCCGCCGCCGCCCTAAGCACC CGGCGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs28364742 Functional Loss DEL dbSNP153 33..38 33 - - - 101541 RMVar_ID_101541 Human_SNP_ID_11933137 m1A Human chr1 - 46198542 46198539 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCC___GCCGCCGCCGCCGCCGCCGCCCTAAGCACC CGGT C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs1393264245 Functional Loss DEL dbSNP153 33..35 33 - - - 101542 RMVar_ID_101542 Human_SNP_ID_11933140 m1A Human chr1 - 46198542 46198542 46198542 CTGGCTGCTTACACCCCGACGCCGCTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC CTGGCTGCTTACACCCCGACGCCGCTGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCTAAGCACC T C POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:46198324..46198629 26863196 MeRIP-seq:(Medium) rs12089669 Functional Loss SNV dbSNP153 33..33 33 - - - 101543 RMVar_ID_101543 Human_SNP_ID_11934432 m1A Human chr1 - 46203529 46203529 46203529 GAGCAGCAGGGCGCCAGAGGTTCCCAGCTCACACTCGCCTCGCAGCCCGCGGAGCAGCCCTTCAG GAGCAGCAGGGCGCCAGAGGTTCCCAGCTCACTCTCGCCTCGCAGCCCGCGGAGCAGCCCTTCAG T A POMGNT1 Ensembl:ENSG00000085998 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:46203431..46203529 32194978 MeRIP-seq:(Medium) rs1322235126 Functional Loss SNV dbSNP153 33..33 33 - - - 101544 RMVar_ID_101544 Human_SNP_ID_11945093 m1A Human chr1 - 46247806 46247806 46247806 TGAAAAGAGCGACAGAGATAGACGCAGACCCCAGCACCTCTCTCTCAACCTTCCTGTTCCCAAAG TGAAAAGAGCGACAGAGATAGACGCAGACCCCCGCACCTCTCTCTCAACCTTCCTGTTCCCAAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46247718..46248004 26863196 MeRIP-seq:(Medium) rs10437093 Functional Loss SNV dbSNP153 33..33 33 - - - 101545 RMVar_ID_101545 Human_SNP_ID_11945119 m1A Human chr1 - 46247895 46247895 46247895 GGAAACCAGGATCAGACTCAGGGAGGTCGAGCAGGAAGCCACGCGGGCGTGTAAAAAACCCAGGT GGAAACCAGGATCAGACTCAGGGAGGTCGAGCGGGAAGCCACGCGGGCGTGTAAAAAACCCAGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46247736..46248182 26863196 MeRIP-seq:(Medium) rs975274726 Functional Loss SNV dbSNP153 33..33 33 - - - 101546 RMVar_ID_101546 Human_SNP_ID_11945170 m1A Human chr1 - 46248058 46248050 46248059 TGATGGTCCCAGTCCGGGTGAAGGGAGGAGGTAGTTGCGCGGCGGGGCGGGGTGGGATTGGGGGT TGATGGTCCCAGTCCGGGTGAAGGGAGGAGG_________GGCGGGGCGGGGTGGGATTGGGGGT CGCGCAACTA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:46247964..46248085 26863410 MeRIP-seq:(Medium) rs1244338371 Functional Loss DEL dbSNP153 32..40 33 - - - 101547 RMVar_ID_101547 Human_SNP_ID_11945176 m1A Human chr1 - 46248058 46248058 46248058 TGATGGTCCCAGTCCGGGTGAAGGGAGGAGGTAGTTGCGCGGCGGGGCGGGGTGGGATTGGGGGT TGATGGTCCCAGTCCGGGTGAAGGGAGGAGGTTGTTGCGCGGCGGGGCGGGGTGGGATTGGGGGT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:46247964..46248085 26863410 MeRIP-seq:(Medium) rs1419003298 Functional Loss SNV dbSNP153 33..33 33 - - - 101548 RMVar_ID_101548 Human_SNP_ID_11948194 m1A Human chr1 + 46260733 46260733 46260733 GTGGACTGAAGGCTGTTATTCTCTAGGGAGTGAAATTCCTGTGGGAGTGTGTCACCAGTCGGCGC GTGGACTGAAGGCTGTTATTCTCTAGGGAGTGGAATTCCTGTGGGAGTGTGTCACCAGTCGGCGC A G RAD54L Ensembl:ENSG00000085999 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46258696..46260767 32194978 MeRIP-seq:(Medium) rs930986495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4056579,Human_RBP_ID_5331627,Human_RBP_ID_19041356,Human_RBP_ID_26865907 Human_Splice_Rec_65356,Human_Splice_Rec_65390,Human_Splice_Rec_65404,Human_Splice_Rec_65440,Human_Splice_Rec_65452,Human_Splice_Rec_65488,Human_Splice_Rec_65502,Human_Splice_Rec_65542,Human_Splice_Rec_65554 RMVar_hsa_circ_25388,RMVar_hsa_circ_50139,RMVar_hsa_circ_82919,RMVar_hsa_circ_113076,RMVar_hsa_circ_132634,RMVar_hsa_circ_53368,RMVar_hsa_circ_132633 101549 RMVar_ID_101549 Human_SNP_ID_11948195 m1A Human chr1 + 46260733 46260733 46260733 GTGGACTGAAGGCTGTTATTCTCTAGGGAGTGAAATTCCTGTGGGAGTGTGTCACCAGTCGGCGC GTGGACTGAAGGCTGTTATTCTCTAGGGAGTGTAATTCCTGTGGGAGTGTGTCACCAGTCGGCGC A T RAD54L Ensembl:ENSG00000085999 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46258696..46260767 32194978 MeRIP-seq:(Medium) rs930986495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4056579,Human_RBP_ID_5331627,Human_RBP_ID_19041356,Human_RBP_ID_26865907 Human_Splice_Rec_65356,Human_Splice_Rec_65390,Human_Splice_Rec_65404,Human_Splice_Rec_65440,Human_Splice_Rec_65452,Human_Splice_Rec_65488,Human_Splice_Rec_65502,Human_Splice_Rec_65542,Human_Splice_Rec_65554 RMVar_hsa_circ_25388,RMVar_hsa_circ_50139,RMVar_hsa_circ_82919,RMVar_hsa_circ_113076,RMVar_hsa_circ_132634,RMVar_hsa_circ_53368,RMVar_hsa_circ_132633 101550 RMVar_ID_101550 Human_SNP_ID_11950467 m1A Human chr1 - 46270717 46270717 46270717 TCTCCTAGCTGCCTGTCTGCCTCACTAGCAGCAGCGTCTCGACCCTTCAAAATTGGCAATTCAAA TCTCCTAGCTGCCTGTCTGCCTCACTAGCAGCGGCGTCTCGACCCTTCAAAATTGGCAATTCAAA T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46270667..46272676 32194978 MeRIP-seq:(Medium) rs1189938053 Functional Loss SNV dbSNP153 33..33 33 - - - 101551 RMVar_ID_101551 Human_SNP_ID_11952445 m1A Human chr1 - 46278182 46278182 46278182 CATCCCAGGCAGCCTGGAGTACCTCATCCCGGAGCCCCCACTTATCAGTGCAGTGGTTCCACCCT CATCCCAGGCAGCCTGGAGTACCTCATCCCGGCGCCCCCACTTATCAGTGCAGTGGTTCCACCCT T G LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46274576..46278374 32194978 MeRIP-seq:(Medium) rs777178522 Functional Loss SNV dbSNP153 33..33 33 - - - 101552 RMVar_ID_101552 Human_SNP_ID_11953360 m1A Human chr1 - 46281254 46281254 46281254 CACCACTGCCCATCCTGGAGCTGACACGTGCTATCGTGCGAGCACTGCCCCTGCTACGGGTCCTC CACCACTGCCCATCCTGGAGCTGACACGTGCTGTCGTGCGAGCACTGCCCCTGCTACGGGTCCTC T C LRRC41 Ensembl:ENSG00000132128 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46281151..46281354 26863196 MeRIP-seq:(Medium) rs769614266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5832377,Human_RBP_ID_8313080,Human_RBP_ID_8749909,Human_RBP_ID_9270133,Human_RBP_ID_18187119,Human_RBP_ID_18965491,Human_RBP_ID_22025935 Human_miRNA_ID_2456116,Human_miRNA_ID_2461025,Human_miRNA_ID_2633682,Human_miRNA_ID_2636369 RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_87705,RMVar_hsa_circ_132640 101553 RMVar_ID_101553 Human_SNP_ID_11954373 m1A Human chr1 + 46285300 46285300 46285300 CCCCAATTTGCCCCTCCCACCTCCCTAGAATTAGGCACACAGCTGGTGCTGCTAGGCAATCTAAG CCCCAATTTGCCCCTCCCACCTCCCTAGAATTGGGCACACAGCTGGTGCTGCTAGGCAATCTAAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46285299..46285399 32194978 MeRIP-seq:(Medium) rs1387435564 Functional Loss SNV dbSNP153 33..33 33 - - - 101554 RMVar_ID_101554 Human_SNP_ID_11954405 m1A Human chr1 - 46285417 46285417 46285417 GTTCCACTCTCCACAGAGGCAGCCCTGACACTATGCCACCTGCTGAGCTCCTGGGTGTCACTGGA GTTCCACTCTCCACAGAGGCAGCCCTGACACTGTGCCACCTGCTGAGCTCCTGGGTGTCACTGGA T C LRRC41 Ensembl:ENSG00000132128 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:46285351..46285600 32194978 MeRIP-seq:(Medium) rs112191997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356733,Human_RBP_ID_860006,Human_RBP_ID_4056714,Human_RBP_ID_8749913,Human_RBP_ID_17453409,Human_RBP_ID_22023320,Human_RBP_ID_22144472 Human_Splice_Rec_65647,Human_Splice_Rec_65659,Human_Splice_Rec_65677,Human_Splice_Rec_65695,Human_Splice_Rec_65711 Human_miRNA_ID_2219320,Human_miRNA_ID_2290825,Human_miRNA_ID_2356172,Human_miRNA_ID_2482355,Human_miRNA_ID_3058616,Human_miRNA_ID_3070732 RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_87705,RMVar_hsa_circ_132640,RMVar_hsa_circ_26204,RMVar_hsa_circ_132641,RMVar_hsa_circ_99832,RMVar_hsa_circ_272836,RMVar_hsa_circ_132642 101555 RMVar_ID_101555 Human_SNP_ID_11954550 m1A Human chr1 - 46285808 46285808 46285808 GAGGGAGCTGCACCCCCCAGCCACCTCCCATGAGGCTCCTGGCACCAAGCGGTCACCTTCTGCTC GAGGGAGCTGCACCCCCCAGCCACCTCCCATGGGGCTCCTGGCACCAAGCGGTCACCTTCTGCTC T C LRRC41 Ensembl:ENSG00000132128 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46285758..46285936 26863196 MeRIP-seq:(Medium) rs773161292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19154316,Human_RBP_ID_27184221 Human_miRNA_ID_2208216,Human_miRNA_ID_2991527,Human_miRNA_ID_3032822 RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_87705,RMVar_hsa_circ_132640,RMVar_hsa_circ_26204,RMVar_hsa_circ_132641,RMVar_hsa_circ_99832,RMVar_hsa_circ_272836,RMVar_hsa_circ_132642 101556 RMVar_ID_101556 Human_SNP_ID_11954551 m1A Human chr1 - 46285808 46285808 46285808 GAGGGAGCTGCACCCCCCAGCCACCTCCCATGAGGCTCCTGGCACCAAGCGGTCACCTTCTGCTC GAGGGAGCTGCACCCCCCAGCCACCTCCCATGCGGCTCCTGGCACCAAGCGGTCACCTTCTGCTC T G LRRC41 Ensembl:ENSG00000132128 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46285758..46285936 26863196 MeRIP-seq:(Medium) rs773161292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19154316,Human_RBP_ID_27184221 Human_miRNA_ID_2208216,Human_miRNA_ID_2991527,Human_miRNA_ID_3032822 RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_87705,RMVar_hsa_circ_132640,RMVar_hsa_circ_26204,RMVar_hsa_circ_132641,RMVar_hsa_circ_99832,RMVar_hsa_circ_272836,RMVar_hsa_circ_132642 101557 RMVar_ID_101557 Human_SNP_ID_11958447 m1A Human chr1 - 46301776 46301776 46301776 CCTGGAAGCGGCGCGGGGGAGGTTCCACCAGGAGGCCTTGCGGGTGGCCGTGGCGTCTTTGCAGG CCTGGAAGCGGCGCGGGGGAGGTTCCACCAGGCGGCCTTGCGGGTGGCCGTGGCGTCTTTGCAGG T G LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:46301754..46301896 26863196 MeRIP-seq:(Medium) rs752585067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258988,Human_RBP_ID_3328404,Human_RBP_ID_5233943,Human_RBP_ID_5311701,Human_RBP_ID_8167057,Human_RBP_ID_9410584,Human_RBP_ID_17204202 RMVar_hsa_circ_111609,RMVar_hsa_circ_132644 101558 RMVar_ID_101558 Human_SNP_ID_11958549 m1A Human chr1 + 46302082 46302082 46302082 GTCCCCAACCCACAGCCCCGCCTCCCAGCCCAACTGGCCGGTTCGCCCTCCCCGGCCGTTCATCC GTCCCCAACCCACAGCCCCGCCTCCCAGCCCAGCTGGCCGGTTCGCCCTCCCCGGCCGTTCATCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:46301435..46302318 26863196 MeRIP-seq:(Medium) rs1169117781 Functional Loss SNV dbSNP153 33..33 33 - - - 101559 RMVar_ID_101559 Human_SNP_ID_11958786 m1A Human chr1 - 46302882 46302882 46302882 CGGCCTGGCTCGGGGGCGCGGGGGGCGAGGCCAGGAGGCCCGGTCTGGAGCGAAGCAGGCTGGGC CGGCCTGGCTCGGGGGCGCGGGGGGCGAGGCCGGGAGGCCCGGTCTGGAGCGAAGCAGGCTGGGC T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46302851..46302954 26863196 MeRIP-seq:(Medium) rs1278378975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221853,Human_RBP_ID_258991,Human_RBP_ID_803559,Human_RBP_ID_3328415,Human_RBP_ID_5159463,Human_RBP_ID_5311706,Human_RBP_ID_5335483,Human_RBP_ID_8051764,Human_RBP_ID_8168019,Human_RBP_ID_8724689,Human_RBP_ID_9412562,Human_RBP_ID_17099296,Human_RBP_ID_18474002,Human_RBP_ID_18928355,Human_RBP_ID_22559072,Human_RBP_ID_22707743,Human_RBP_ID_22735127,Human_RBP_ID_26773608 RMVar_hsa_circ_111609,RMVar_hsa_circ_132644 101560 RMVar_ID_101560 Human_SNP_ID_11959124 m1A Human chr1 + 46303747 46303747 46303747 GGGTTAGGTGCCGCTGTTGCTGCTCGTGTTGAATCTAGAACCGTAGCCAGACATGGGACTGGAGG GGGTTAGGTGCCGCTGTTGCTGCTCGTGTTGAGTCTAGAACCGTAGCCAGACATGGGACTGGAGG A G UQCRH Ensembl:ENSG00000173660 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr1:46303701..46303862;chr1:46303701..46303858;chr1:46303701..46303870;chr1:46303701..46303825 26863196 MeRIP-seq:(Medium) rs764555192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356743,Human_RBP_ID_744158,Human_RBP_ID_978703,Human_RBP_ID_1154914,Human_RBP_ID_1432282,Human_RBP_ID_1749255,Human_RBP_ID_4072796,Human_RBP_ID_5457770,Human_RBP_ID_8313126,Human_RBP_ID_8970882,Human_RBP_ID_11011927,Human_RBP_ID_22144510,Human_RBP_ID_22430602,Human_RBP_ID_22785265,Human_RBP_ID_23205162,Human_RBP_ID_23399102,Human_RBP_ID_26380894,Human_RBP_ID_26865999,Human_RBP_ID_27184236,Human_RBP_ID_27555526 Human_Splice_Rec_65729,Human_Splice_Rec_65735,Human_Splice_Rec_65741,Human_Splice_Rec_65743 RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 101561 RMVar_ID_101561 Human_SNP_ID_11960660 m1A Human chr1 - 46310095 46310094 46310096 ATGGGCATTTTTAGCAGAGACCCACCAAACACATATGCTTTGATTAACACAACCACCAAACCAAG ATGGGCATTTTTAGCAGAGACCCACCAAACA__TATGCTTTGATTAACACAACCACCAAACCAAG ATG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:46310092..46310346 26863196 MeRIP-seq:(Medium) rs913171755 Functional Loss DEL dbSNP153 32..33 33 - - - 101562 RMVar_ID_101562 Human_SNP_ID_11960756 m1A Human chr1 + 46310300 46310300 46310300 GGATTGCACGGAGGAGCTCTTTGACTTCTTGCATGCGAGGGACCATTGCGTAAGTCAGTGGGAAG GGATTGCACGGAGGAGCTCTTTGACTTCTTGCGTGCGAGGGACCATTGCGTAAGTCAGTGGGAAG A G UQCRH Ensembl:ENSG00000173660 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:46310249..46316750 32194978 MeRIP-seq:(Medium) rs772789538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356749,Human_RBP_ID_744167,Human_RBP_ID_978705,Human_RBP_ID_5108631,Human_RBP_ID_8970885,Human_RBP_ID_11012125,Human_RBP_ID_17647558,Human_RBP_ID_17752792,Human_RBP_ID_18187127,Human_RBP_ID_19038148,Human_RBP_ID_22430606,Human_RBP_ID_22469744,Human_RBP_ID_22488353,Human_RBP_ID_23399124,Human_RBP_ID_26798363 Human_Splice_Rec_65733,Human_Splice_Rec_65739,Human_Splice_Rec_65749,Human_Splice_Rec_65751 RMVar_hsa_circ_127847,RMVar_hsa_circ_132646,RMVar_hsa_circ_299483,RMVar_hsa_circ_296731,RMVar_hsa_circ_132647 101563 RMVar_ID_101563 Human_SNP_ID_11970217 m1A Human chr1 + 46343730 46343730 46343730 AACACAAGTCAGGGCCAGAGTGAGAGTCCCCAACTTAGCATAAATGAGCACCAGGGTGAGAGTCC AACACAAGTCAGGGCCAGAGTGAGAGTCCCCAGCTTAGCATAAATGAGCACCAGGGTGAGAGTCC A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:46343723..46343868 26863196 MeRIP-seq:(Medium) rs747001832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94338,RMVar_hsa_circ_132649 101564 RMVar_ID_101564 Human_SNP_ID_11975364 m1A Human chr1 + 46363028 46363028 46363028 TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTATATAATTTTAGAATACCTGAAGGCTTCTTGGC TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTGTATAATTTTAGAATACCTGAAGGCTTCTTGGC A G NSUN4 Ensembl:ENSG00000117481 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17361833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012630,Human_RBP_ID_19373009,Human_RBP_ID_26386039,Human_RBP_ID_27595369 GWAS_ID_13371,GWAS_ID_13372,GWAS_ID_13373,GWAS_ID_13374 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649 101565 RMVar_ID_101565 Human_SNP_ID_11975365 m1A Human chr1 + 46363028 46363028 46363028 TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTATATAATTTTAGAATACCTGAAGGCTTCTTGGC TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTTTATAATTTTAGAATACCTGAAGGCTTCTTGGC A T NSUN4 Ensembl:ENSG00000117481 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17361833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012630,Human_RBP_ID_19373009,Human_RBP_ID_26386039,Human_RBP_ID_27595369 GWAS_ID_13371,GWAS_ID_13372,GWAS_ID_13373,GWAS_ID_13374 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649 101566 RMVar_ID_101566 Human_SNP_ID_12006399 m1A Human chr1 + 46490198 46490198 46490198 AAGTGAGCAACTTAGGGAGACAGAAAGAGCGCAGAACTCGAAATTCCGAGGCAGAGAGAGCGGAG AAGTGAGCAACTTAGGGAGACAGAAAGAGCGCTGAACTCGAAATTCCGAGGCAGAGAGAGCGGAG A T DMBX1 Ensembl:ENSG00000197587 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:46489837..46490210 26863196 MeRIP-seq:(Medium) rs1366071872 Functional Loss SNV dbSNP153 33..33 33 - - - 101567 RMVar_ID_101567 Human_SNP_ID_12010558 m1A Human chr1 - 46507078 46507078 46507078 CATGCTGGGCCTGCTGGGCTGCCTGCTGGTGCAGGTTGTACATGGCGCTGAGTGAGTTCATGGCG CATGCTGGGCCTGCTGGGCTGCCTGCTGGTGCGGGTTGTACATGGCGCTGAGTGAGTTCATGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46507009..46507107 26863196 MeRIP-seq:(Medium) rs573920919 Functional Loss SNV dbSNP153 33..33 33 - - - 101568 RMVar_ID_101568 Human_SNP_ID_12024741 m1A Human chr1 - 46562022 46562022 46562022 AGAAGGAACAGCACGGGCATAGATGTGGGCACATGAAATAGCTGGAGTGTCTAGGAAGGAAGAGT AGAAGGAACAGCACGGGCATAGATGTGGGCACGTGAAATAGCTGGAGTGTCTAGGAAGGAAGAGT T C MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:46561972..46562088 26863196 MeRIP-seq:(Medium) rs1029550495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96009,RMVar_hsa_circ_117691,RMVar_hsa_circ_111909,RMVar_hsa_circ_132655,RMVar_hsa_circ_132657,RMVar_hsa_circ_89218,RMVar_hsa_circ_132656,RMVar_hsa_circ_132654 101569 RMVar_ID_101569 Human_SNP_ID_12029860 m1A Human chr1 - 46583327 46583327 46583327 GTTTCCCTTACATCTCCTCTTATCTCCTAGAGATGGGCAGTAGCGAACCCCTTCCCATCGCAGAT GTTTCCCTTACATCTCCTCTTATCTCCTAGAGGTGGGCAGTAGCGAACCCCTTCCCATCGCAGAT T C MKNK1 Ensembl:ENSG00000079277 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46583276..46583361 26863196 MeRIP-seq:(Medium) rs754995712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854703,Human_RBP_ID_26311214,Human_RBP_ID_27798004 Human_Splice_Rec_66002,Human_Splice_Rec_66003,Human_Splice_Rec_66028,Human_Splice_Rec_66029,Human_Splice_Rec_66052,Human_Splice_Rec_66053,Human_Splice_Rec_66074,Human_Splice_Rec_66075,Human_Splice_Rec_66094,Human_Splice_Rec_66095,Human_Splice_Rec_66116,Human_Splice_Rec_66117,Human_Splice_Rec_66142,Human_Splice_Rec_66143,Human_Splice_Rec_66170,Human_Splice_Rec_66171,Human_Splice_Rec_66190,Human_Splice_Rec_66191,Human_Splice_Rec_66224,Human_Splice_Rec_66225,Human_Splice_Rec_66252,Human_Splice_Rec_66253,Human_Splice_Rec_66266,Human_Splice_Rec_66267,Human_Splice_Rec_66280,Human_Splice_Rec_66281,Human_Splice_Rec_66292,Human_Splice_Rec_66293,Human_Splice_Rec_66306,Human_Splice_Rec_66307,Human_Splice_Rec_66314,Human_Splice_Rec_66315,Human_Splice_Rec_66322,Human_Splice_Rec_66323,Human_Splice_Rec_66330,Human_Splice_Rec_66331,Human_Splice_Rec_66338,Human_Splice_Rec_66339,Human_Splice_Rec_66344,Human_Splice_Rec_66345,Human_Splice_Rec_66350,Human_Splice_Rec_66351,Human_Splice_Rec_66356,Human_Splice_Rec_66357 RMVar_hsa_circ_11797,RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_310662,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_127728,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_24627,RMVar_hsa_circ_132668,RMVar_hsa_circ_37976,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 101570 RMVar_ID_101570 Human_SNP_ID_12037411 m1A Human chr1 - 46616790 46616790 46616790 GCAGGACAGGCAGACGGACAGGCTGACAGGAGAGAGAACAGGCACTGCGGGACCTGCAGGAGAAA GCAGGACAGGCAGACGGACAGGCTGACAGGAGGGAGAACAGGCACTGCGGGACCTGCAGGAGAAA T C MKNK1,MOB3C Ensembl:ENSG00000079277,Ensembl:ENSG00000142961 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46616548..46616853 26863196 MeRIP-seq:(Medium) rs564227621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_66335,Human_Splice_Rec_66371,Human_Splice_Rec_66387 101571 RMVar_ID_101571 Human_SNP_ID_12049136 m1A Human chr1 + 46668312 46668312 46668312 CCGGTCCCGCGCCACCCGCAGCCGCCACCACCACAGCAGCCATGGCCGCCCCCGCCTCCTCCTCC CCGGTCCCGCGCCACCCGCAGCCGCCACCACCGCAGCAGCCATGGCCGCCCCCGCCTCCTCCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:46668051..46668419 26863196 MeRIP-seq:(Medium) rs759596200 Functional Loss SNV dbSNP153 33..33 33 - - - 101572 RMVar_ID_101572 Human_SNP_ID_12049137 m1A Human chr1 + 46668314 46668314 46668314 GGTCCCGCGCCACCCGCAGCCGCCACCACCACAGCAGCCATGGCCGCCCCCGCCTCCTCCTCCTC GGTCCCGCGCCACCCGCAGCCGCCACCACCACGGCAGCCATGGCCGCCCCCGCCTCCTCCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:46668020..46668426;chr1:46668022..46668422 26863196 MeRIP-seq:(Medium) rs1331209620 Functional Loss SNV dbSNP153 33..33 33 - - - 101573 RMVar_ID_101573 Human_SNP_ID_12060926 m1A Human chr1 - 46718215 46718215 46718215 GGCGGATCTGGTCAGTCCCACCCCTAGGTGGGAGTGACCAGGGGGCTCTGGCCCAGGATTCCCAA GGCGGATCTGGTCAGTCCCACCCCTAGGTGGGGGTGACCAGGGGGCTCTGGCCCAGGATTCCCAA T C EFCAB14 Ensembl:ENSG00000159658 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46718165..46718266 32194978 MeRIP-seq:(Medium) rs1050811513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222554,Human_RBP_ID_4097109,Human_RBP_ID_11014220,Human_RBP_ID_21910570,Human_RBP_ID_22023336,Human_RBP_ID_22144556 Human_miRNA_ID_2435816,Human_miRNA_ID_2679297,Human_miRNA_ID_2866888,Human_miRNA_ID_2995813 RMVar_hsa_circ_80614,RMVar_hsa_circ_132678 101574 RMVar_ID_101574 Human_SNP_ID_12061212 m1A Human chr1 + 46719074 46719074 46719074 TGGTGGCGGCGGCTGCGGCGGCGGCGGCCGCGAGCTCCAGCCCCGGGCCATCGCTCCAGCCCCAG TGGTGGCGGCGGCTGCGGCGGCGGCGGCCGCGGGCTCCAGCCCCGGGCCATCGCTCCAGCCCCAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:46718951..46719125;chr1:46718597..46719125;chr1:46718771..46719125;chr1:46718759..46719125 26863196 MeRIP-seq:(Medium) rs1269639774 Functional Loss SNV dbSNP153 33..33 33 - - - 101575 RMVar_ID_101575 Human_SNP_ID_12061216 m1A Human chr1 - 46719077 46719077 46719077 GATCTGGGGCTGGAGCGATGGCCCGGGGCTGGAGCTCGCGGCCGCCGCCGCCGCAGCCGCCGCCA GATCTGGGGCTGGAGCGATGGCCCGGGGCTGGGGCTCGCGGCCGCCGCCGCCGCAGCCGCCGCCA T C EFCAB14 Ensembl:ENSG00000159658 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr1:46718886..46719125;chr1:46718926..46719106 26863196 MeRIP-seq:(Medium) rs1288062000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4057166,Human_RBP_ID_18430530 101576 RMVar_ID_101576 Human_SNP_ID_12206077 m1A Human chr1 + 47314092 47314092 47314092 TGTTTGCAGGGTAGGAGCGGGAGCCGGCTCCAAGGAGCGCCACCGCCGACTCCGGCCCCGCCTCT TGTTTGCAGGGTAGGAGCGGGAGCCGGCTCCAGGGAGCGCCACCGCCGACTCCGGCCCCGCCTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:47313908..47314093 26863196 MeRIP-seq:(Medium) rs1431319256 Functional Loss SNV dbSNP153 33..33 33 - - - 101577 RMVar_ID_101577 Human_SNP_ID_12210780 m1A Human chr1 + 47333977 47333977 47333977 TATGCTGAGCCGCTGCCGCAGCGGGCTGCTCCACGTCCTGGGCCTTAGCTTCCTGCTGCAGACCC TATGCTGAGCCGCTGCCGCAGCGGGCTGCTCCCCGTCCTGGGCCTTAGCTTCCTGCTGCAGACCC A C CMPK1 Ensembl:ENSG00000162368 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr1:47333841..47334056;chr1:47333872..47334051;chr1:47333926..47334000 26863196,32194978 MeRIP-seq:(Medium) rs758840728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224389,Human_RBP_ID_357081,Human_RBP_ID_4072804,Human_RBP_ID_22025941 101578 RMVar_ID_101578 Human_SNP_ID_12210809 m1A Human chr1 - 47334025 47334025 47334025 CGACCAGCGGCTTCATGAGACGTGGAGAGCAGAGGAGAATCGGCCGGCGGGTCTGCAGCAGGAAG CGACCAGCGGCTTCATGAGACGTGGAGAGCAGGGGAGAATCGGCCGGCGGGTCTGCAGCAGGAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:47333846..47358327;chr1:47333857..47334156 26863196 MeRIP-seq:(Medium) rs773308240 Functional Loss SNV dbSNP153 33..33 33 - - - 101579 RMVar_ID_101579 Human_SNP_ID_12220542 m1A Human chr1 + 47373100 47373100 47373100 AGATGTATCTTTCGTTCTCTTTTTTGACTGTAATAATGAGGTAATGAAAATCTTCATCTGCCCAC AGATGTATCTTTCGTTCTCTTTTTTGACTGTAGTAATGAGGTAATGAAAATCTTCATCTGCCCAC A G CMPK1 Ensembl:ENSG00000162368 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:47373076..47373100 32194978 MeRIP-seq:(Medium) rs1285303122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_357089,Human_RBP_ID_2151022,Human_RBP_ID_9342741,Human_RBP_ID_18231189 Human_Splice_Rec_67635,Human_Splice_Rec_67645,Human_Splice_Rec_67653 Human_miRNA_ID_1976383 RMVar_hsa_circ_47874,RMVar_hsa_circ_292288,RMVar_hsa_circ_303006,RMVar_hsa_circ_367188,RMVar_hsa_circ_132716,RMVar_hsa_circ_132717,RMVar_hsa_circ_275971 101580 RMVar_ID_101580 Human_SNP_ID_12221452 m1A Human chr1 - 47377418 47377418 47377418 TAGATGTGATCCTTGCCCCATACCCTTAGATTATGTCAGACTAAAGCTGACAATTCTGCCAGGCT TAGATGTGATCCTTGCCCCATACCCTTAGATTGTGTCAGACTAAAGCTGACAATTCTGCCAGGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:47377291..47377591 32194978 MeRIP-seq:(Medium) rs1020424309 Functional Loss SNV dbSNP153 33..33 33 - - - 101581 RMVar_ID_101581 Human_SNP_ID_12235848 m1A Human chr1 + 47438127 47438127 47438127 GAGCGGAGCCGGAGAGTGGCGGCGGCGGCGGCAGCGGCACCATGACCCTGGGCAGCTGCTGCTGC GAGCGGAGCCGGAGAGTGGCGGCGGCGGCGGCGGCGGCACCATGACCCTGGGCAGCTGCTGCTGC A G FOXD2 Ensembl:ENSG00000186564 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:47438080..47438313;chr1:47438076..47438348 26863196 MeRIP-seq:(Medium) rs1335309782 Functional Loss SNV dbSNP153 33..33 33 - - - 101582 RMVar_ID_101582 Human_SNP_ID_12354803 m1A Human chr1 - 47937120 47937118 47937121 TCATGGTAGTGGTAATGATGGTGATGGTGATGATCATGCTGGTGGTGGTGGTGATGATCATGGTA TCATGGTAGTGGTAATGATGGTGATGGTGAT___CATGCTGGTGGTGGTGGTGATGATCATGGTA GATC G TRABD2B Ensembl:ENSG00000269113 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:47937075..47937150 26863196 MeRIP-seq:(Medium) rs1348972248 Functional Loss DEL dbSNP153 32..34 33 - - - 101583 RMVar_ID_101583 Human_SNP_ID_12354805 m1A Human chr1 - 47937120 47937120 47937120 TCATGGTAGTGGTAATGATGGTGATGGTGATGATCATGCTGGTGGTGGTGGTGATGATCATGGTA TCATGGTAGTGGTAATGATGGTGATGGTGATGTTCATGCTGGTGGTGGTGGTGATGATCATGGTA T A TRABD2B Ensembl:ENSG00000269113 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:47937075..47937150 26863196 MeRIP-seq:(Medium) rs1281692947 Functional Loss SNV dbSNP153 33..33 33 - - - 101584 RMVar_ID_101584 Human_SNP_ID_12354845 m1A Human chr1 + 47937224 47937219 47937225 TCACCATCATCATCACCACTACCATGATCATCACCATCACCACCACCACCATGATCATCACCATC TCACCATCATCATCACCACTACCATGAT______CATCACCACCACCACCATGATCATCACCATC TCATCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:47937183..47937375 26863196 MeRIP-seq:(Medium) rs199665913 Functional Loss DEL dbSNP153 29..34 33 - - - 101585 RMVar_ID_101585 Human_SNP_ID_12369627 m1A Human chr1 + 47997661 47997661 47997661 ACGCGCGGAGGGAGGCGAAGCCCGCAGCAGCCACTTCCCAACTTTCCAAACTTCCCAGCGCAACT ACGCGCGGAGGGAGGCGAAGCCCGCAGCAGCCGCTTCCCAACTTTCCAAACTTCCCAGCGCAACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:47997588..47997688 26863196 MeRIP-seq:(Medium) rs1175184398 Functional Loss SNV dbSNP153 33..33 33 - - - 101586 RMVar_ID_101586 Human_SNP_ID_12480593 m1A Human chr1 - 48453128 48453128 48453128 TTACATCCATTTTATCTAATTTCTTTCAGGTAACTTGCCCAGGAGTCGTGCTTAAAGACAAAGAG TTACATCCATTTTATCTAATTTCTTTCAGGTAGCTTGCCCAGGAGTCGTGCTTAAAGACAAAGAG T C SPATA6 Ensembl:ENSG00000132122 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:48453102..48453187 26863410 MeRIP-seq:(Medium) rs756833028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_67898,Human_Splice_Rec_67922,Human_Splice_Rec_67944,Human_Splice_Rec_68010,Human_Splice_Rec_68020,Human_Splice_Rec_68036 RMVar_hsa_circ_112176,RMVar_hsa_circ_132722,RMVar_hsa_circ_372001,RMVar_hsa_circ_132727,RMVar_hsa_circ_362419,RMVar_hsa_circ_313668,RMVar_hsa_circ_265349,RMVar_hsa_circ_132732,RMVar_hsa_circ_286127 101587 RMVar_ID_101587 Human_SNP_ID_12945375 m1A Human chr1 - 50475556 50475556 50475556 GTGGCGAGTTCTTGGAGCGGCGTTTCCTGGCCAGCAACAAGCTCCAGATTGTCTTTGATTTTGTA GTGGCGAGTTCTTGGAGCGGCGTTTCCTGGCCGGCAACAAGCTCCAGATTGTCTTTGATTTTGTA T C FAF1 Ensembl:ENSG00000185104 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:50475451..50490621 32194978 MeRIP-seq:(Medium) rs1259334134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9358823,Human_RBP_ID_22870840,Human_RBP_ID_26311222 Human_Splice_Rec_68465,Human_Splice_Rec_68489,Human_Splice_Rec_68519 Human_miRNA_ID_2791260 RMVar_hsa_circ_132746,RMVar_hsa_circ_330052,RMVar_hsa_circ_365419,RMVar_hsa_circ_372233,RMVar_hsa_circ_337978,RMVar_hsa_circ_31875,RMVar_hsa_circ_312519,RMVar_hsa_circ_132747,RMVar_hsa_circ_132748 101588 RMVar_ID_101588 Human_SNP_ID_12996022 m1A Human chr1 - 50692430 50692430 50692430 GGTGTGGACGGGTAGGAATGAGGAAAGCGGAGATGTTGGTCAAAGGATACAGTTTCAGTTTGACA GGTGTGGACGGGTAGGAATGAGGAAAGCGGAGTTGTTGGTCAAAGGATACAGTTTCAGTTTGACA T A FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:50692428..50692495 26863196 MeRIP-seq:(Medium) rs935553824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17066573 RMVar_hsa_circ_372233,RMVar_hsa_circ_132748,RMVar_hsa_circ_342372,RMVar_hsa_circ_98037,RMVar_hsa_circ_121195,RMVar_hsa_circ_57665,RMVar_hsa_circ_132758,RMVar_hsa_circ_132749,RMVar_hsa_circ_132750,RMVar_hsa_circ_351618,RMVar_hsa_circ_346580,RMVar_hsa_circ_290494,RMVar_hsa_circ_120153,RMVar_hsa_circ_62423,RMVar_hsa_circ_132762,RMVar_hsa_circ_322742,RMVar_hsa_circ_73327,RMVar_hsa_circ_266772,RMVar_hsa_circ_377068,RMVar_hsa_circ_115678,RMVar_hsa_circ_132774,RMVar_hsa_circ_266651,RMVar_hsa_circ_302183,RMVar_hsa_circ_132770,RMVar_hsa_circ_132771,RMVar_hsa_circ_320543,RMVar_hsa_circ_296445,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_293283,RMVar_hsa_circ_3800,RMVar_hsa_circ_132775,RMVar_hsa_circ_132772,RMVar_hsa_circ_132773 101589 RMVar_ID_101589 Human_SNP_ID_13060556 m1A Human chr1 - 50959323 50959323 50959323 TTTATATTGTATTAAGGGAAGAGTAAAAAAGCAGAATGATGAGATGGCGAGGGCAATGACAATGG TTTATATTGTATTAAGGGAAGAGTAAAAAAGCCGAATGATGAGATGGCGAGGGCAATGACAATGG T G FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:50959321..50959425 26863196 MeRIP-seq:(Medium) rs1222377510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11021768,Human_RBP_ID_21963003,Human_RBP_ID_23400611 RMVar_hsa_circ_124880,RMVar_hsa_circ_132788 101590 RMVar_ID_101590 Human_SNP_ID_13060786 m1A Human chr1 - 50960007 50960007 50960007 GCAGGTTGCAGGCGGGCGGCCGGGGCGCCTGAAGGTTACCGAGTGCATGAGCGCCTAGCGCTTCC GCAGGTTGCAGGCGGGCGGCCGGGGCGCCTGAGGGTTACCGAGTGCATGAGCGCCTAGCGCTTCC T C FAF1 Ensembl:ENSG00000185104 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:50959912..50960013 26863410 MeRIP-seq:(Medium) rs934032615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072805,Human_RBP_ID_9356328 RMVar_hsa_circ_124880,RMVar_hsa_circ_132788 101591 RMVar_ID_101591 Human_SNP_ID_13060794 m1A Human chr1 - 50960037 50960037 50960037 TCCTGTCCGGGCTGCTGCGACGCGGGCTCCGCAGGTTGCAGGCGGGCGGCCGGGGCGCCTGAAGG TCCTGTCCGGGCTGCTGCGACGCGGGCTCCGCGGGTTGCAGGCGGGCGGCCGGGGCGCCTGAAGG T C FAF1 Ensembl:ENSG00000185104 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:50959987..50960226 26863196 MeRIP-seq:(Medium) rs1476426228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_357266,Human_RBP_ID_4057685,Human_RBP_ID_9356328,Human_RBP_ID_18430559 RMVar_hsa_circ_124880,RMVar_hsa_circ_132788 101592 RMVar_ID_101592 Human_SNP_ID_13060804 m1A Human chr1 + 50960057 50960057 50960057 CCGCCTGCAACCTGCGGAGCCCGCGTCGCAGCAGCCCGGACAGGAAGATTGGTCTGGATGTGGGT CCGCCTGCAACCTGCGGAGCCCGCGTCGCAGCGGCCCGGACAGGAAGATTGGTCTGGATGTGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:50960008..50960209;chr1:50960009..50960219 26863196 MeRIP-seq:(Medium) rs1340004189 Functional Loss SNV dbSNP153 33..33 33 - - - 101593 RMVar_ID_101593 Human_SNP_ID_13060807 m1A Human chr1 + 50960066 50960066 50960066 ACCTGCGGAGCCCGCGTCGCAGCAGCCCGGACAGGAAGATTGGTCTGGATGTGGGTCCGGTCTTA ACCTGCGGAGCCCGCGTCGCAGCAGCCCGGACGGGAAGATTGGTCTGGATGTGGGTCCGGTCTTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:50960015..50960228 26863196 MeRIP-seq:(Medium) rs1346987190 Functional Loss SNV dbSNP153 33..33 33 - - - 101594 RMVar_ID_101594 Human_SNP_ID_13063059 m1A Human chr1 - 50969724 50969724 50969724 ACGTGCTCCGGAGGGTTAAAAGATGATCGCCAAAGGCGAACGGGAGTAGCAGTTCGGTGGCCCTC ACGTGCTCCGGAGGGTTAAAAGATGATCGCCAGAGGCGAACGGGAGTAGCAGTTCGGTGGCCCTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:50969701..50969725 26863196 MeRIP-seq:(Medium) rs1323891524 Functional Loss SNV dbSNP153 33..33 33 - - - 101595 RMVar_ID_101595 Human_SNP_ID_13064847 m1A Human chr1 - 50977835 50977835 50977835 GAAGACACTCCAAAGTCCGGGGAGGGAAGTCAAGCTGAGAGGCAGGCCGGCATCTGGGCAGGGGG GAAGACACTCCAAAGTCCGGGGAGGGAAGTCAGGCTGAGAGGCAGGCCGGCATCTGGGCAGGGGG T C lnc-FAF1-1 RNACentral:URS00008C2F39 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:50977784..50978053;chr1:50977784..50977868 26863196 MeRIP-seq:(Medium) rs1220579556 Functional Loss SNV dbSNP153 33..33 33 - - - 101596 RMVar_ID_101596 Human_SNP_ID_13123937 m1A Human chr1 - 51236374 51236374 51236374 GCGGCCGTCGCGGCTGCCTCAGCTGCTGCCTCAGCTGCTGCTGCCCCCGCCGACGCCGGAGCCAC GCGGCCGTCGCGGCTGCCTCAGCTGCTGCCTCGGCTGCTGCTGCCCCCGCCGACGCCGGAGCCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:51236325..51236401;chr1:51236324..51236410 26863196 MeRIP-seq:(Medium) rs1029080590 Functional Loss SNV dbSNP153 33..33 33 - - - 101597 RMVar_ID_101597 Human_SNP_ID_13124028 m1A Human chr1 - 51236513 51236513 51236513 GGGTCGCGGCGTTCGCCTCCTGCGAGGCAGCGATGGGGGGGGGGGGGCGGGGAGACGAAGCACTT GGGTCGCGGCGTTCGCCTCCTGCGAGGCAGCGGTGGGGGGGGGGGGGCGGGGAGACGAAGCACTT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:51236320..51236519 26863410 MeRIP-seq:(Medium) rs1159913219 Functional Loss SNV dbSNP153 33..33 33 - - - 101598 RMVar_ID_101598 Human_SNP_ID_13124084 m1A Human chr1 + 51236706 51236706 51236706 CCAACCGAGGCGGACCGCGGAGTGTGCGAACGACCCCACCGCTGCTTTCTCCTCCCCCAGATCAC CCAACCGAGGCGGACCGCGGAGTGTGCGAACGGCCCCACCGCTGCTTTCTCCTCCCCCAGATCAC A G RNF11 Ensembl:ENSG00000123091 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:51236526..51236725;chr1:51236501..51236825 26863196 MeRIP-seq:(Medium) rs765047688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_357307,Human_RBP_ID_17338201,Human_RBP_ID_27399618 101599 RMVar_ID_101599 Human_SNP_ID_13194190 m1A Human chr1 - 51519236 51519236 51519236 CCGTCTTCCTTCCCCTCCCTTGCATGATGGAAACACCATGGCTGCGGCGGCCCAGCTCTCTCTGA CCGTCTTCCTTCCCCTCCCTTGCATGATGGAAGCACCATGGCTGCGGCGGCCCAGCTCTCTCTGA T C EPS15 Ensembl:ENSG00000085832 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:51519153..51519328 26863196 MeRIP-seq:(Medium) rs759017975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_357477 Human_Splice_Rec_68947,Human_Splice_Rec_68991,Human_Splice_Rec_69059,Human_Splice_Rec_69083,Human_Splice_Rec_69097 RMVar_hsa_circ_117028,RMVar_hsa_circ_132847 101600 RMVar_ID_101600 Human_SNP_ID_13194192 m1A Human chr1 + 51519241 51519241 51519241 GAGAGCTGGGCCGCCGCAGCCATGGTGTTTCCATCATGCAAGGGAGGGGAAGGAAGACGGGCTGA GAGAGCTGGGCCGCCGCAGCCATGGTGTTTCCCTCATGCAAGGGAGGGGAAGGAAGACGGGCTGA A C EPS15-AS1 Ensembl:ENSG00000227070 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51519159..51519278 26863196 MeRIP-seq:(Medium) rs764490216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5540800 101601 RMVar_ID_101601 Human_SNP_ID_13217590 m1A Human chr1 - 51620575 51620575 51620575 CCTTTGTCTCAAGCACTTTTCCCTCTCTGCTCATACGGCTAATCTCTCCTCATCATTCAAGTCAA CCTTTGTCTCAAGCACTTTTCCCTCTCTGCTCTTACGGCTAATCTCTCCTCATCATTCAAGTCAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51620573..51620727 26863196 MeRIP-seq:(Medium) rs1019939303 Functional Loss SNV dbSNP153 33..33 33 - - - 101602 RMVar_ID_101602 Human_SNP_ID_13254556 m1A Human chr1 + 51786584 51786584 51786584 GAAGTTGCCTATAATCAAGAAGAAAGTGAGGAAGTTGGAAGATCAGAACGAGTATGAATCCCGCA GAAGTTGCCTATAATCAAGAAGAAAGTGAGGAGGTTGGAAGATCAGAACGAGTATGAATCCCGCA A G OSBPL9 Ensembl:ENSG00000117859 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:51786534..51787420 32194978 MeRIP-seq:(Medium) rs141360356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1750014,Human_RBP_ID_5537942,Human_RBP_ID_5837843,Human_RBP_ID_9342106,Human_RBP_ID_11025050,Human_RBP_ID_23401189,Human_RBP_ID_24541474 Human_Splice_Rec_69200,Human_Splice_Rec_69201,Human_Splice_Rec_69242,Human_Splice_Rec_69243,Human_Splice_Rec_69286,Human_Splice_Rec_69287,Human_Splice_Rec_69328,Human_Splice_Rec_69329,Human_Splice_Rec_69372,Human_Splice_Rec_69373,Human_Splice_Rec_69414,Human_Splice_Rec_69415,Human_Splice_Rec_69524,Human_Splice_Rec_69525,Human_Splice_Rec_69560,Human_Splice_Rec_69561,Human_Splice_Rec_69652,Human_Splice_Rec_69653,Human_Splice_Rec_69686,Human_Splice_Rec_69687,Human_Splice_Rec_69740,Human_Splice_Rec_69741,Human_Splice_Rec_69763,Human_Splice_Rec_69778,Human_Splice_Rec_69779 RMVar_hsa_circ_65077,RMVar_hsa_circ_23372,RMVar_hsa_circ_274615,RMVar_hsa_circ_132874,RMVar_hsa_circ_132875,RMVar_hsa_circ_60789 101603 RMVar_ID_101603 Human_SNP_ID_13254774 m1A Human chr1 + 51787440 51787440 51787440 GAAGCAAAGCACAGGCTTGAAGAAAGACAAAGAGCAGAAGCCCGAGAAAGGAAGGAGAAGGAAAT GAAGCAAAGCACAGGCTTGAAGAAAGACAAAGTGCAGAAGCCCGAGAAAGGAAGGAGAAGGAAAT A T OSBPL9 Ensembl:ENSG00000117859 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:51787391..51787500 26863196 MeRIP-seq:(Medium) rs1459099926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854727,Human_RBP_ID_19034893,Human_RBP_ID_22425997,Human_RBP_ID_23255535,Human_RBP_ID_24541800,Human_RBP_ID_24708581 Human_Splice_Rec_69202,Human_Splice_Rec_69203,Human_Splice_Rec_69244,Human_Splice_Rec_69245,Human_Splice_Rec_69288,Human_Splice_Rec_69289,Human_Splice_Rec_69330,Human_Splice_Rec_69331,Human_Splice_Rec_69374,Human_Splice_Rec_69375,Human_Splice_Rec_69416,Human_Splice_Rec_69417,Human_Splice_Rec_69526,Human_Splice_Rec_69527,Human_Splice_Rec_69562,Human_Splice_Rec_69563,Human_Splice_Rec_69654,Human_Splice_Rec_69655,Human_Splice_Rec_69688,Human_Splice_Rec_69689,Human_Splice_Rec_69742,Human_Splice_Rec_69743,Human_Splice_Rec_69764,Human_Splice_Rec_69765,Human_Splice_Rec_69780,Human_Splice_Rec_69781 Human_miRNA_ID_1767163 RMVar_hsa_circ_65077,RMVar_hsa_circ_274615,RMVar_hsa_circ_132874,RMVar_hsa_circ_132875 101604 RMVar_ID_101604 Human_SNP_ID_13255858 m1A Human chr1 + 51790614 51790614 51790614 CAGTTCCTATCCACCTCCTCCCCAAGGTGGGTATCCTCACACTCCTTCAGCTTGATGAGAGCTGT CAGTTCCTATCCACCTCCTCCCCAAGGTGGGTGTCCTCACACTCCTTCAGCTTGATGAGAGCTGT A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:51790496..51790680 26863196 MeRIP-seq:(Medium) rs756644281 Functional Loss SNV dbSNP153 33..33 33 - - - 101605 RMVar_ID_101605 Human_SNP_ID_13255979 m1A Human chr1 - 51790961 51790959 51790961 CAGTTCTGAAGTTGTTGATAAGAAGATAGAAGAGTTTCTTTCTAGCTTTGAGGAGAAGATTGAGA CAGTTCTGAAGTTGTTGATAAGAAGATAGAAG__TTTCTTTCTAGCTTTGAGGAGAAGATTGAGA ACT A NRDC Ensembl:ENSG00000078618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:51790853..51791005 26863196 MeRIP-seq:(Medium) rs1273096396 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1750027,Human_RBP_ID_3936084,Human_RBP_ID_23401198 Human_Splice_Rec_69808,Human_Splice_Rec_69809,Human_Splice_Rec_69866,Human_Splice_Rec_69867,Human_Splice_Rec_69928,Human_Splice_Rec_69929,Human_Splice_Rec_69990,Human_Splice_Rec_69991,Human_Splice_Rec_70046,Human_Splice_Rec_70047,Human_Splice_Rec_70104,Human_Splice_Rec_70105 RMVar_hsa_circ_34023,RMVar_hsa_circ_371730,RMVar_hsa_circ_57926,RMVar_hsa_circ_67541,RMVar_hsa_circ_132877,RMVar_hsa_circ_378118,RMVar_hsa_circ_103767,RMVar_hsa_circ_132878,RMVar_hsa_circ_132879 101606 RMVar_ID_101606 Human_SNP_ID_13257119 m1A Human chr1 - 51795769 51795768 51795769 ATTTCTTTCTTGAAGCAGTGGGTTGGTGGAACAGGAACAGTAGTAAGAGTGGGAGCATATGAGGA ATTTCTTTCTTGAAGCAGTGGGTTGGTGGAAC_GGAACAGTAGTAAGAGTGGGAGCATATGAGGA CT C NRDC Ensembl:ENSG00000078618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51795765..51795853 26863196 MeRIP-seq:(Medium) rs1477750192 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5837876 RMVar_hsa_circ_34023,RMVar_hsa_circ_371730,RMVar_hsa_circ_67541,RMVar_hsa_circ_132877,RMVar_hsa_circ_378118,RMVar_hsa_circ_103767,RMVar_hsa_circ_132878,RMVar_hsa_circ_132881,RMVar_hsa_circ_331,RMVar_hsa_circ_78166,RMVar_hsa_circ_132879,RMVar_hsa_circ_132880,RMVar_hsa_circ_308754 101607 RMVar_ID_101607 Human_SNP_ID_13260152 m1A Human chr1 + 51809382 51809382 51809382 GGATTTAATTCGAAATTACTATTCCACAGTTCAGCCCAAGAGTTTTCAATATCTGTAAAGGAGAA GGATTTAATTCGAAATTACTATTCCACAGTTCTGCCCAAGAGTTTTCAATATCTGTAAAGGAGAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:51809333..51810313 32194978 MeRIP-seq:(Medium) rs1265627144 Functional Loss SNV dbSNP153 33..33 33 - - - 101608 RMVar_ID_101608 Human_SNP_ID_13263629 m1A Human chr1 - 51825312 51825312 51825312 GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGACATCCTATGGGAAAATTTTTTTGGGGTAAGAT GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGGCATCCTATGGGAAAATTTTTTTGGGGTAAGAT T C NRDC Ensembl:ENSG00000078618 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11205896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1750062,Human_RBP_ID_3316471,Human_RBP_ID_8750111,Human_RBP_ID_9252940,Human_RBP_ID_9270142 Human_Splice_Rec_69824,Human_Splice_Rec_69825,Human_Splice_Rec_69886,Human_Splice_Rec_69887,Human_Splice_Rec_69948,Human_Splice_Rec_69949,Human_Splice_Rec_70006,Human_Splice_Rec_70007,Human_Splice_Rec_70062,Human_Splice_Rec_70063,Human_Splice_Rec_70130,Human_Splice_Rec_70131,Human_Splice_Rec_70150 GWAS_ID_13375,GWAS_ID_13376,GWAS_ID_13377,GWAS_ID_13378,GWAS_ID_13379 RMVar_hsa_circ_3432,RMVar_hsa_circ_34023,RMVar_hsa_circ_103767,RMVar_hsa_circ_132881,RMVar_hsa_circ_78166,RMVar_hsa_circ_132879,RMVar_hsa_circ_132880,RMVar_hsa_circ_308754,RMVar_hsa_circ_12321,RMVar_hsa_circ_11979,RMVar_hsa_circ_132883,RMVar_hsa_circ_132887,RMVar_hsa_circ_344326,RMVar_hsa_circ_303176,RMVar_hsa_circ_55941,RMVar_hsa_circ_132888,RMVar_hsa_circ_294881,RMVar_hsa_circ_74765,RMVar_hsa_circ_343054,RMVar_hsa_circ_356702,RMVar_hsa_circ_53311,RMVar_hsa_circ_132894,RMVar_hsa_circ_364064,RMVar_hsa_circ_347463,RMVar_hsa_circ_276938,RMVar_hsa_circ_11179,RMVar_hsa_circ_66780,RMVar_hsa_circ_132899,RMVar_hsa_circ_360507,RMVar_hsa_circ_62314,RMVar_hsa_circ_280188,RMVar_hsa_circ_340806,RMVar_hsa_circ_303293,RMVar_hsa_circ_132902,RMVar_hsa_circ_41692,RMVar_hsa_circ_132901,RMVar_hsa_circ_291210,RMVar_hsa_circ_355688,RMVar_hsa_circ_62713,RMVar_hsa_circ_5550,RMVar_hsa_circ_132903,RMVar_hsa_circ_132904,RMVar_hsa_circ_48711,RMVar_hsa_circ_60868,RMVar_hsa_circ_274550,RMVar_hsa_circ_343639,RMVar_hsa_circ_359022,RMVar_hsa_circ_362060,RMVar_hsa_circ_294034,RMVar_hsa_circ_132906,RMVar_hsa_circ_132907,RMVar_hsa_circ_98685,RMVar_hsa_circ_132908 101609 RMVar_ID_101609 Human_SNP_ID_13263630 m1A Human chr1 - 51825312 51825312 51825312 GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGACATCCTATGGGAAAATTTTTTTGGGGTAAGAT GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGCCATCCTATGGGAAAATTTTTTTGGGGTAAGAT T G NRDC Ensembl:ENSG00000078618 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11205896 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1750062,Human_RBP_ID_3316471,Human_RBP_ID_8750111,Human_RBP_ID_9252940,Human_RBP_ID_9270142 Human_Splice_Rec_69824,Human_Splice_Rec_69825,Human_Splice_Rec_69886,Human_Splice_Rec_69887,Human_Splice_Rec_69948,Human_Splice_Rec_69949,Human_Splice_Rec_70006,Human_Splice_Rec_70007,Human_Splice_Rec_70062,Human_Splice_Rec_70063,Human_Splice_Rec_70130,Human_Splice_Rec_70131,Human_Splice_Rec_70150 GWAS_ID_13375,GWAS_ID_13376,GWAS_ID_13377,GWAS_ID_13378,GWAS_ID_13379 RMVar_hsa_circ_3432,RMVar_hsa_circ_34023,RMVar_hsa_circ_103767,RMVar_hsa_circ_132881,RMVar_hsa_circ_78166,RMVar_hsa_circ_132879,RMVar_hsa_circ_132880,RMVar_hsa_circ_308754,RMVar_hsa_circ_12321,RMVar_hsa_circ_11979,RMVar_hsa_circ_132883,RMVar_hsa_circ_132887,RMVar_hsa_circ_344326,RMVar_hsa_circ_303176,RMVar_hsa_circ_55941,RMVar_hsa_circ_132888,RMVar_hsa_circ_294881,RMVar_hsa_circ_74765,RMVar_hsa_circ_343054,RMVar_hsa_circ_356702,RMVar_hsa_circ_53311,RMVar_hsa_circ_132894,RMVar_hsa_circ_364064,RMVar_hsa_circ_347463,RMVar_hsa_circ_276938,RMVar_hsa_circ_11179,RMVar_hsa_circ_66780,RMVar_hsa_circ_132899,RMVar_hsa_circ_360507,RMVar_hsa_circ_62314,RMVar_hsa_circ_280188,RMVar_hsa_circ_340806,RMVar_hsa_circ_303293,RMVar_hsa_circ_132902,RMVar_hsa_circ_41692,RMVar_hsa_circ_132901,RMVar_hsa_circ_291210,RMVar_hsa_circ_355688,RMVar_hsa_circ_62713,RMVar_hsa_circ_5550,RMVar_hsa_circ_132903,RMVar_hsa_circ_132904,RMVar_hsa_circ_48711,RMVar_hsa_circ_60868,RMVar_hsa_circ_274550,RMVar_hsa_circ_343639,RMVar_hsa_circ_359022,RMVar_hsa_circ_362060,RMVar_hsa_circ_294034,RMVar_hsa_circ_132906,RMVar_hsa_circ_132907,RMVar_hsa_circ_98685,RMVar_hsa_circ_132908 101610 RMVar_ID_101610 Human_SNP_ID_13276971 m1A Human chr1 + 51878534 51878534 51878534 GTCTTCGCACCGACCCCGCGTTTCGATTCCCCAGAGCGCCGCGAGCTCCCGCCCGGCCTCACACA GTCTTCGCACCGACCCCGCGTTTCGATTCCCCGGAGCGCCGCGAGCTCCCGCCCGGCCTCACACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:51878433..51878775 26863196 MeRIP-seq:(Medium) rs759671627 Functional Loss SNV dbSNP153 33..33 33 - - - 101611 RMVar_ID_101611 Human_SNP_ID_13277040 m1A Human chr1 - 51878684 51878678 51878684 CCGCGGCTGCGGCAGCACCAGGGCCGGCCGCCACCGCCTCTAGAACGCGGAGGAGGTGGGTCCTG CCGCGGCTGCGGCAGCACCAGGGCCGGCCGCC______TCTAGAACGCGGAGGAGGTGGGTCCTG AGGCGGT A NRDC Ensembl:ENSG00000078618 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:51878414..51878775 26863196 MeRIP-seq:(Medium) rs1427052600 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4058275,Human_RBP_ID_5519004,Human_RBP_ID_9270148,Human_RBP_ID_18414962,Human_RBP_ID_18468577,Human_RBP_ID_22023374,Human_RBP_ID_22144813,Human_RBP_ID_26311280,Human_RBP_ID_26866394,Human_RBP_ID_27798039 Human_miRNA_ID_2797209,Human_miRNA_ID_2798176,Human_miRNA_ID_2799556,Human_miRNA_ID_2806872,Human_miRNA_ID_2810016,Human_miRNA_ID_2813158,Human_miRNA_ID_2832747,Human_miRNA_ID_2852271,Human_miRNA_ID_2853333,Human_miRNA_ID_2860414 RMVar_hsa_circ_121225,RMVar_hsa_circ_132913 101612 RMVar_ID_101612 Human_SNP_ID_13277050 m1A Human chr1 - 51878697 51878697 51878697 TCAGGCCTGTTCCCCGCGGCTGCGGCAGCACCAGGGCCGGCCGCCACCGCCTCTAGAACGCGGAG TCAGGCCTGTTCCCCGCGGCTGCGGCAGCACCGGGGCCGGCCGCCACCGCCTCTAGAACGCGGAG T C NRDC Ensembl:ENSG00000078618 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51878326..51878775 26863196 MeRIP-seq:(Medium) rs971483887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17711,Human_RBP_ID_741646,Human_RBP_ID_858817,Human_RBP_ID_4058275,Human_RBP_ID_5519004,Human_RBP_ID_9270148,Human_RBP_ID_18414962,Human_RBP_ID_18468577,Human_RBP_ID_22023374,Human_RBP_ID_26311280,Human_RBP_ID_26866394,Human_RBP_ID_27798039 RMVar_hsa_circ_121225,RMVar_hsa_circ_132913 101613 RMVar_ID_101613 Human_SNP_ID_13313270 m1A Human chr1 - 52033314 52033314 52033314 AGGAGGACGGGAGAGCCCAGGCGGCGGGCAGCAGCGTCCTCAGGGAACTGCATACTGCGGACTCT AGGAGGACGGGAGAGCCCAGGCGGCGGGCAGCGGCGTCCTCAGGGAACTGCATACTGCGGACTCT T C AL445685.3,KTI12,TXNDC12 Ensembl:ENSG00000285839,Ensembl:ENSG00000198841,Ensembl:ENSG00000117862 Protein coding,Protein coding,Protein coding CDS,CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:52033273..52033399 26863196 MeRIP-seq:(Medium) rs1386650049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 101614 RMVar_ID_101614 Human_SNP_ID_13313302 m1A Human chr1 - 52033371 52033371 52033371 CGGGCGCGAACGAGAACCCTGGCCGGAACGTCAGTGTGAGTTGGCGGCCACGCGCTGAGGAGGAC CGGGCGCGAACGAGAACCCTGGCCGGAACGTCTGTGTGAGTTGGCGGCCACGCGCTGAGGAGGAC T A KTI12,TXNDC12 Ensembl:ENSG00000198841,Ensembl:ENSG00000117862 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:52033277..52033473 26863410 MeRIP-seq:(Medium) rs777503714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27399680 RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 101615 RMVar_ID_101615 Human_SNP_ID_13313303 m1A Human chr1 - 52033371 52033371 52033371 CGGGCGCGAACGAGAACCCTGGCCGGAACGTCAGTGTGAGTTGGCGGCCACGCGCTGAGGAGGAC CGGGCGCGAACGAGAACCCTGGCCGGAACGTCGGTGTGAGTTGGCGGCCACGCGCTGAGGAGGAC T C KTI12,TXNDC12 Ensembl:ENSG00000198841,Ensembl:ENSG00000117862 Protein coding,Protein coding CDS,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:52033277..52033473 26863410 MeRIP-seq:(Medium) rs777503714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27399680 RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 101616 RMVar_ID_101616 Human_SNP_ID_13313439 m1A Human chr1 + 52033661 52033661 52033661 CCTCTGCGCCCAGGACAGCTGCGTCGTCCACCACGTACACCGCGCGGCCCTCGGCAGCCAGCGCC CCTCTGCGCCCAGGACAGCTGCGTCGTCCACCGCGTACACCGCGCGGCCCTCGGCAGCCAGCGCC A G AL445685.1 Ensembl:ENSG00000223390 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:52033633..52033752 26863196 MeRIP-seq:(Medium) rs765776605 Functional Loss SNV dbSNP153 33..33 33 - - - 101617 RMVar_ID_101617 Human_SNP_ID_13313498 m1A Human chr1 + 52033768 52033768 52033768 AGCCCGCAAAACACCACGAGCGGCATCCTCTCAGGGAGCGACCATTGGCAACCGCGCTGCGCCAA AGCCCGCAAAACACCACGAGCGGCATCCTCTCGGGGAGCGACCATTGGCAACCGCGCTGCGCCAA A G AL445685.1 Ensembl:ENSG00000223390 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:52033668..52033767 26863410 MeRIP-seq:(Medium) rs1321775540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_70217 101618 RMVar_ID_101618 Human_SNP_ID_13318717 m1A Human chr1 - 52056352 52056352 52056352 CTCACCTGAAGCAGGGAGGGTCCTCCAACACCAGCACGCGGCAAGAGAAAGATGGCTGCCTCAGC CTCACCTGAAGCAGGGAGGGTCCTCCAACACCCGCACGCGGCAAGAGAAAGATGGCTGCCTCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:52056302..52056400 26863196 MeRIP-seq:(Medium) rs1276138244 Functional Loss SNV dbSNP153 33..33 33 - - - 101619 RMVar_ID_101619 Human_SNP_ID_13353721 m1A Human chr1 + 52197586 52197586 52197586 GGGTAGAAGAGGAGGAGTCAGGGATGAAGATGAGAGATAGATGTCAAAAAAAAATAGAAGAAAGT GGGTAGAAGAGGAGGAGTCAGGGATGAAGATGCGAGATAGATGTCAAAAAAAAATAGAAGAAAGT A C ZFYVE9 Ensembl:ENSG00000157077 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:52197574..52197639 26863196 MeRIP-seq:(Medium) rs1435862689 Functional Loss SNV dbSNP153 33..33 33 - - - 101620 RMVar_ID_101620 Human_SNP_ID_13353749 m1A Human chr1 - 52197661 52197661 52197661 CATTCAATTATTAGATCACATCCTCCTCCTTTATGAAACTCTTCTTCCATGACTTGTGTGATACT CATTCAATTATTAGATCACATCCTCCTCCTTTGTGAAACTCTTCTTCCATGACTTGTGTGATACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:52197660..52197787 26863196 MeRIP-seq:(Medium) rs904554576 Functional Loss SNV dbSNP153 33..33 33 - - - 101621 RMVar_ID_101621 Human_SNP_ID_13392454 m1A Human chr1 - 52353635 52353635 52353635 CCTCTCTGTGGTCCTCACAGGTCCTGGATGGAAGGAAGCCCACCGGGGGGAAGCTGGAGGTGAAG CCTCTCTGTGGTCCTCACAGGTCCTGGATGGACGGAAGCCCACCGGGGGGAAGCTGGAGGTGAAG T G CC2D1B Ensembl:ENSG00000154222 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:52353493..52353668 26863196 MeRIP-seq:(Medium) rs945384041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854736,Human_RBP_ID_3936101,Human_RBP_ID_4058653,Human_RBP_ID_18965536,Human_RBP_ID_22633721,Human_RBP_ID_22871303 Human_Splice_Rec_70410,Human_Splice_Rec_70458,Human_Splice_Rec_70546,Human_Splice_Rec_70582,Human_Splice_Rec_70583,Human_Splice_Rec_70622,Human_Splice_Rec_70658,Human_Splice_Rec_70664 RMVar_hsa_circ_57248 101622 RMVar_ID_101622 Human_SNP_ID_13394879 m1A Human chr1 + 52360168 52360168 52360168 GGGGCCAGGGGCCGCTTTCCTAAGGCCACTGGAGGTGGGATCTCATCCTCATTGATCTTTCTGCC GGGGCCAGGGGCCGCTTTCCTAAGGCCACTGGCGGTGGGATCTCATCCTCATTGATCTTTCTGCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:52360039..52360243 26863196 MeRIP-seq:(Medium) rs936673935 Functional Loss SNV dbSNP153 33..33 33 - - - 101623 RMVar_ID_101623 Human_SNP_ID_13395323 m1A Human chr1 - 52361453 52361453 52361453 GCTCTGAGGCAAGCTTGGGCCTGGTGGAGGAGAGGGCAGTGGAGAGGAGGCTGGGGGTGCCCCTG GCTCTGAGGCAAGCTTGGGCCTGGTGGAGGAGCGGGCAGTGGAGAGGAGGCTGGGGGTGCCCCTG T G CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:52361451..52361651 26863196 MeRIP-seq:(Medium) rs1003753573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_804652,Human_RBP_ID_850038,Human_RBP_ID_5333302,Human_RBP_ID_9318945,Human_RBP_ID_9342763,Human_RBP_ID_17101869,Human_RBP_ID_19034910,Human_RBP_ID_26767505 RMVar_hsa_circ_132948,RMVar_hsa_circ_100223,RMVar_hsa_circ_85362,RMVar_hsa_circ_132950 101624 RMVar_ID_101624 Human_SNP_ID_13395348 m1A Human chr1 + 52361525 52361525 52361525 TACCAGCCTGGCAGACACACCAGCAGCTCTGCATCTTCCTCCAGCCCTTCCTCCTCCTCCTCCTC TACCAGCCTGGCAGACACACCAGCAGCTCTGCGTCTTCCTCCAGCCCTTCCTCCTCCTCCTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:52361001..52362685 26863196 MeRIP-seq:(Medium) rs755672233 Functional Loss SNV dbSNP153 33..33 33 - - - 101625 RMVar_ID_101625 Human_SNP_ID_13396593 m1A Human chr1 + 52366048 52366048 52366048 TACCCCCGCGGTCCCCAGAACTCCCCACGCCGAGGGGCGGGGACGCGGCATACCTCGCGGTGAAT TACCCCCGCGGTCCCCAGAACTCCCCACGCCGGGGGGCGGGGACGCGGCATACCTCGCGGTGAAT A G AL513218.2 Ensembl:ENSG00000287078 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:52366043..52366148 26863196 MeRIP-seq:(Medium) rs923580578 Functional Loss SNV dbSNP153 33..33 33 - - - 101626 RMVar_ID_101626 Human_SNP_ID_13413163 m1A Human chr1 - 52431169 52431169 52431169 TCCATGGCCCAGTGATCCACTCTGCACCAGGCAGTGCCCCCAGCAATATTGGCCTAAATGATCCC TCCATGGCCCAGTGATCCACTCTGCACCAGGCGGTGCCCCCAGCAATATTGGCCTAAATGATCCC T C TUT4 Ensembl:ENSG00000134744 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:52431121..52431394 26863196 MeRIP-seq:(Medium) rs776348312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11028901,Human_RBP_ID_17071510,Human_RBP_ID_17223383,Human_RBP_ID_18577527,Human_RBP_ID_22144900 Human_Splice_Rec_70938 Human_miRNA_ID_2048733,Human_miRNA_ID_2682732 RMVar_hsa_circ_45435,RMVar_hsa_circ_88452,RMVar_hsa_circ_107636,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132971,RMVar_hsa_circ_132974,RMVar_hsa_circ_332780,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_132973 101627 RMVar_ID_101627 Human_SNP_ID_13477039 m1A Human chr1 - 52698292 52698292 52698292 GGCCGGCATGGTGGACTTCCAGGATGAGGAGCAGGTCAAGTCCTTTTTGGAGAACATGGAGGTGG GGCCGGCATGGTGGACTTCCAGGATGAGGAGCGGGTCAAGTCCTTTTTGGAGAACATGGAGGTGG T C COA7 Ensembl:ENSG00000162377 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:52697948..52698350;chr1:52697916..52698302 26863196 MeRIP-seq:(Medium) rs756032188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1432677,Human_RBP_ID_1750464,Human_RBP_ID_4074055,Human_RBP_ID_5840239,Human_RBP_ID_18968431,Human_RBP_ID_22871614 Human_Splice_Rec_71153 101628 RMVar_ID_101628 Human_SNP_ID_13496154 m1A Human chr1 - 52772270 52772270 52772270 TCTGATAGAGAGCCAGATTCACCGTTTGGCTCAATATTATAAGACCAAGCGAGTCCTCCCTCCCA TCTGATAGAGAGCCAGATTCACCGTTTGGCTCGATATTATAAGACCAAGCGAGTCCTCCCTCCCA T C RPS13P2 Ensembl:ENSG00000228929 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879182143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1866130,Human_miRNA_ID_1866339 101629 RMVar_ID_101629 Human_SNP_ID_13510568 m1A Human chr1 + 52823198 52823198 52823198 ATTTAGGTCTGGATGCAGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAAGCTGAAGCAGGAGG ATTTAGGTCTGGATGCAGTGGCTCATGCTTGTGATCCCAGCACTTTGGGAAGCTGAAGCAGGAGG A G ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97549,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053 101630 RMVar_ID_101630 Human_SNP_ID_13510834 m1A Human chr1 + 52824180 52824179 52824181 AAACTTCCTACTTTTTTTCTTTTTGTAGAGACAGAGTTTCACTCTGTCGCCCAAGCTGGAGTGCA AAACTTCCTACTTTTTTTCTTTTTGTAGAGAC__AGTTTCACTCTGTCGCCCAAGCTGGAGTGCA CAG C ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1300801671 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8750407 RMVar_hsa_circ_97549,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053 101631 RMVar_ID_101631 Human_SNP_ID_13534728 m1A Human chr1 - 52914933 52914933 52914933 GTGGTCGGATTGGGGTAAGAAAGATGACTGTGACCCAAATGTGGGAACGAATGTGTGTGTGCTGG GTGGTCGGATTGGGGTAAGAAAGATGACTGTGGCCCAAATGTGGGAACGAATGTGTGTGTGCTGG T C ECHDC2 Ensembl:ENSG00000121310 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:52914757..52914997 26863196 MeRIP-seq:(Medium) rs996433070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23263195 101632 RMVar_ID_101632 Human_SNP_ID_13536335 m1A Human chr1 - 52921686 52921686 52921686 CGGTGCAGGGCCGGAGAAGCACCTTCACTCCCAGCCTGCGCCCCGATGCTGCGCGTTCTGTGCCT CGGTGCAGGGCCGGAGAAGCACCTTCACTCCCGGCCTGCGCCCCGATGCTGCGCGTTCTGTGCCT T C ECHDC2 Ensembl:ENSG00000121310 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:52921510..52921703 26863196 MeRIP-seq:(Medium) rs758167745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18414965,Human_RBP_ID_18577745 101633 RMVar_ID_101633 Human_SNP_ID_13537663 m1A Human chr1 - 52927387 52927387 52927387 GGCTCCCACGGGGAAGAGGACATGGCTGCACCAGTGCGGGACCGGGGCGGGCGCCGCGGACGACT GGCTCCCACGGGGAAGAGGACATGGCTGCACCTGTGCGGGACCGGGGCGGGCGCCGCGGACGACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:52927338..52927514 26863196 MeRIP-seq:(Medium) rs756943613 Functional Loss SNV dbSNP153 33..33 33 - - - 101634 RMVar_ID_101634 Human_SNP_ID_13557740 m1A Human chr1 - 53015026 53015026 53015026 CTGAATGTCACTCACCTGGCGGCTTCCGGAAAACCCATCTTGTAGAGTGTTACAACCACAGCTCC CTGAATGTCACTCACCTGGCGGCTTCCGGAAAGCCCATCTTGTAGAGTGTTACAACCACAGCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53014976..53015079 26863196 MeRIP-seq:(Medium) rs758417010 Functional Loss SNV dbSNP153 33..33 33 - - - 101635 RMVar_ID_101635 Human_SNP_ID_13557741 m1A Human chr1 - 53015026 53015026 53015026 CTGAATGTCACTCACCTGGCGGCTTCCGGAAAACCCATCTTGTAGAGTGTTACAACCACAGCTCC CTGAATGTCACTCACCTGGCGGCTTCCGGAAACCCCATCTTGTAGAGTGTTACAACCACAGCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53014976..53015079 26863196 MeRIP-seq:(Medium) rs758417010 Functional Loss SNV dbSNP153 33..33 33 - - - 101636 RMVar_ID_101636 Human_SNP_ID_13603667 m1A Human chr1 + 53196867 53196867 53196867 TCAGGAGTCCTGACGCAGTGTCTTGGGCGCTAACGGCGGCGGCGGCCTTGTGTTTAGACTCCAGA TCAGGAGTCCTGACGCAGTGTCTTGGGCGCTAGCGGCGGCGGCGGCCTTGTGTTTAGACTCCAGA A G CPT2 Ensembl:ENSG00000157184 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:53196818..53197050;chr1:53196821..53197048;chr1:53196823..53197005 26863196 MeRIP-seq:(Medium) rs1256940049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4059415,Human_RBP_ID_5486569 101637 RMVar_ID_101637 Human_SNP_ID_13609322 m1A Human chr1 - 53218923 53218923 53218923 AGCTGCTTTACTAACATTCTTTTTCCCCAAAGATGAAATGTGGCAACTGTGGTGAGATTTCGGAC AGCTGCTTTACTAACATTCTTTTTCCCCAAAGGTGAAATGTGGCAACTGTGGTGAGATTTCGGAC T C CZIB Ensembl:ENSG00000162384 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53218921..53219022 26863196 MeRIP-seq:(Medium) rs899587941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3317154,Human_RBP_ID_5841121,Human_RBP_ID_18577791,Human_RBP_ID_22638745 Human_Splice_Rec_72072,Human_Splice_Rec_72073,Human_Splice_Rec_72083,Human_Splice_Rec_72094,Human_Splice_Rec_72095 101638 RMVar_ID_101638 Human_SNP_ID_13609825 m1A Human chr1 - 53220449 53220447 53220450 AGTGGGTGCGCGCTGAAGGAGCAGGAGGCAGAAGGAGTGTCTCCCTGTGGCACCCACGGCTGGGA AGTGGGTGCGCGCTGAAGGAGCAGGAGGCAG___GAGTGTCTCCCTGTGGCACCCACGGCTGGGA CCTT C CZIB Ensembl:ENSG00000162384 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:53220400..53220571 26863196 MeRIP-seq:(Medium) rs549996186 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8314518,Human_RBP_ID_22871798 101639 RMVar_ID_101639 Human_SNP_ID_13609892 m1A Human chr1 + 53220574 53220574 53220574 GTCCCCGCGGCGGGCGGCCTCCCCTCACCCCCATGGTAGCCCTCTCCGCCCGGTGCTGGCTGCGG GTCCCCGCGGCGGGCGGCCTCCCCTCACCCCCCTGGTAGCCCTCTCCGCCCGGTGCTGGCTGCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:53220215..53220625;chr1:53220200..53220625;chr1:53220192..53220625 26863196 MeRIP-seq:(Medium) rs969093308 Functional Loss SNV dbSNP153 33..33 33 - - - 101640 RMVar_ID_101640 Human_SNP_ID_13613657 m1A Human chr1 + 53235622 53235622 53235622 ATGACATCATTCTTGTAATTGCTGTTGTTGGCATATCTTAACTTCCCTGTGGGGGCAAAAAACAA ATGACATCATTCTTGTAATTGCTGTTGTTGGCGTATCTTAACTTCCCTGTGGGGGCAAAAAACAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:53235576..53238525 26863196 MeRIP-seq:(Medium) rs1305245706 Functional Loss SNV dbSNP153 33..33 33 - - - 101641 RMVar_ID_101641 Human_SNP_ID_13614345 m1A Human chr1 - 53238452 53238452 53238452 TCTTGGAAGTTCAGGCTCGGTTGTCTTTTGGGAGCCATGGAGAGTGACTTTTATCTGCGTTACTA TCTTGGAAGTTCAGGCTCGGTTGTCTTTTGGGGGCCATGGAGAGTGACTTTTATCTGCGTTACTA T C MAGOH Ensembl:ENSG00000162385 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1467654602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25416,Human_RBP_ID_1750586,Human_RBP_ID_4074064,Human_RBP_ID_5841264,Human_RBP_ID_17762661,Human_RBP_ID_18577802,Human_RBP_ID_23402502,Human_RBP_ID_24550216 Human_Splice_Rec_72115,Human_Splice_Rec_72123,Human_Splice_Rec_72133 101642 RMVar_ID_101642 Human_SNP_ID_13614351 m1A Human chr1 + 53238461 53238461 53238461 AGATAAAAGTCACTCTCCATGGCTCCCAAAAGACAACCGAGCCTGAACTTCCAAGAGCAAGCCGC AGATAAAAGTCACTCTCCATGGCTCCCAAAAGGCAACCGAGCCTGAACTTCCAAGAGCAAGCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53238319..53238525 26863196 MeRIP-seq:(Medium) rs1460860898 Functional Loss SNV dbSNP153 33..33 33 - - - 101643 RMVar_ID_101643 Human_SNP_ID_13615356 m1A Human chr1 + 53242529 53242529 53242529 GCCTCTGGAAGAGACACCAGACTGCAAAGGGCACCGCGTACAGAAGCTAACGGAACTTGAATGAC GCCTCTGGAAGAGACACCAGACTGCAAAGGGCGCCGCGTACAGAAGCTAACGGAACTTGAATGAC A G AL606760.1 Ensembl:ENSG00000226754 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:53242483..53242565 32194978 MeRIP-seq:(Medium) rs1360055901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_72140,Human_Splice_Rec_72144,Human_Splice_Rec_72145,Human_Splice_Rec_72148 101644 RMVar_ID_101644 Human_SNP_ID_13617951 m1A Human chr1 - 53255150 53255150 53255150 CAAATGAAGACAGTAAGATGGGCTCAACAGTCACTGCCGCTGTTATCGGGATCATCGTGCCCATA CAAATGAAGACAGTAAGATGGGCTCAACAGTCGCTGCCGCTGTTATCGGGATCATCGTGCCCATA T C LRP8 Ensembl:ENSG00000157193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53255126..53255150 26863196 MeRIP-seq:(Medium) rs1162864808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_854756,Human_RBP_ID_26314261,Human_RBP_ID_26800569 Human_Splice_Rec_72178,Human_Splice_Rec_72179,Human_Splice_Rec_72212,Human_Splice_Rec_72213,Human_Splice_Rec_72218,Human_Splice_Rec_72219,Human_Splice_Rec_72246,Human_Splice_Rec_72247,Human_Splice_Rec_72274,Human_Splice_Rec_72275,Human_Splice_Rec_72310,Human_Splice_Rec_72311,Human_Splice_Rec_72342,Human_Splice_Rec_72343,Human_Splice_Rec_72374,Human_Splice_Rec_72375,Human_Splice_Rec_72408,Human_Splice_Rec_72409,Human_Splice_Rec_72416,Human_Splice_Rec_72417,Human_Splice_Rec_72450,Human_Splice_Rec_72451,Human_Splice_Rec_72482,Human_Splice_Rec_72483,Human_Splice_Rec_72506,Human_Splice_Rec_72507,Human_Splice_Rec_72536,Human_Splice_Rec_72537,Human_Splice_Rec_72569,Human_Splice_Rec_72576,Human_Splice_Rec_72577,Human_Splice_Rec_72614,Human_Splice_Rec_72615,Human_Splice_Rec_72650,Human_Splice_Rec_72651,Human_Splice_Rec_72680,Human_Splice_Rec_72681,Human_Splice_Rec_72710,Human_Splice_Rec_72711,Human_Splice_Rec_72740,Human_Splice_Rec_72741,Human_Splice_Rec_72774,Human_Splice_Rec_72775,Human_Splice_Rec_72800,Human_Splice_Rec_72801,Human_Splice_Rec_72808,Human_Splice_Rec_72809,Human_Splice_Rec_72840,Human_Splice_Rec_72841,Human_Splice_Rec_72876,Human_Splice_Rec_72877,Human_Splice_Rec_72894,Human_Splice_Rec_72895,Human_Splice_Rec_72926,Human_Splice_Rec_72927,Human_Splice_Rec_72940,Human_Splice_Rec_72952 RMVar_hsa_circ_10376,RMVar_hsa_circ_321133,RMVar_hsa_circ_47119,RMVar_hsa_circ_330103,RMVar_hsa_circ_377245,RMVar_hsa_circ_317086,RMVar_hsa_circ_133097,RMVar_hsa_circ_3041,RMVar_hsa_circ_360124,RMVar_hsa_circ_371160,RMVar_hsa_circ_133098 101645 RMVar_ID_101645 Human_SNP_ID_13618418 m1A Human chr1 - 53257339 53257339 53257339 CCACCTACCAGAACCACAGCACAGAGACACCAAGCCTGACAGCTGCAGTCCCAAGCTCAGTTAGT CCACCTACCAGAACCACAGCACAGAGACACCAGGCCTGACAGCTGCAGTCCCAAGCTCAGTTAGT T C LRP8 Ensembl:ENSG00000157193 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53257289..53257357 26863196 MeRIP-seq:(Medium) rs1198130161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_72177,Human_Splice_Rec_72217,Human_Splice_Rec_72245,Human_Splice_Rec_72273,Human_Splice_Rec_72309,Human_Splice_Rec_72373,Human_Splice_Rec_72407,Human_Splice_Rec_72415,Human_Splice_Rec_72449,Human_Splice_Rec_72481,Human_Splice_Rec_72505,Human_Splice_Rec_72535,Human_Splice_Rec_72575,Human_Splice_Rec_72613,Human_Splice_Rec_72649,Human_Splice_Rec_72679,Human_Splice_Rec_72709,Human_Splice_Rec_72773,Human_Splice_Rec_72799,Human_Splice_Rec_72807,Human_Splice_Rec_72839,Human_Splice_Rec_72875,Human_Splice_Rec_72893,Human_Splice_Rec_72925,Human_Splice_Rec_72939,Human_Splice_Rec_72951 Human_miRNA_ID_203295,Human_miRNA_ID_1488513,Human_miRNA_ID_2011100,Human_miRNA_ID_2757451 RMVar_hsa_circ_10376,RMVar_hsa_circ_330103,RMVar_hsa_circ_377245,RMVar_hsa_circ_317086,RMVar_hsa_circ_133097,RMVar_hsa_circ_3041,RMVar_hsa_circ_360124,RMVar_hsa_circ_371160,RMVar_hsa_circ_12689,RMVar_hsa_circ_133098 101646 RMVar_ID_101646 Human_SNP_ID_13622841 m1A Human chr1 + 53277576 53277576 53277576 GTGGCTCCATCACCTCACTCCTGAATGTTCGCAGCTCCCGCCATGCTAGACCATTTGCTGGGCCC GTGGCTCCATCACCTCACTCCTGAATGTTCGCGGCTCCCGCCATGCTAGACCATTTGCTGGGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:53277572..53277731 26863196 MeRIP-seq:(Medium) rs974435647 Functional Loss SNV dbSNP153 33..33 33 - - - 101647 RMVar_ID_101647 Human_SNP_ID_13624398 m1A Human chr1 - 53284196 53284192 53284196 AGGTAAGTGGCCCGGGTATGTAGTAGGTAAGTAAGCGGCCCGGGTATGTAGTAGGTAAGTAAGCG AGGTAAGTGGCCCGGGTATGTAGTAGGTAAGT____GGCCCGGGTATGTAGTAGGTAAGTAAGCG CGCTT C LRP8 Ensembl:ENSG00000157193 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:53284178..53284265;chr1:53284181..53284275 26863196 MeRIP-seq:(Medium) rs36210712 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_377245,RMVar_hsa_circ_47114,RMVar_hsa_circ_378223,RMVar_hsa_circ_15517,RMVar_hsa_circ_327970,RMVar_hsa_circ_285923,RMVar_hsa_circ_268781,RMVar_hsa_circ_133106 101648 RMVar_ID_101648 Human_SNP_ID_13624414 m1A Human chr1 + 53284221 53284221 53284221 GGCCGCTTACTTACCTACTACATACCCGGGCCACTTACCTACTACATACCCGGGCCACTTACTTA GGCCGCTTACTTACCTACTACATACCCGGGCCGCTTACCTACTACATACCCGGGCCACTTACTTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:53284160..53284264 26863196 MeRIP-seq:(Medium) rs1445796725 Functional Loss SNV dbSNP153 33..33 33 - - - 101649 RMVar_ID_101649 Human_SNP_ID_13628775 m1A Human chr1 + 53303524 53303523 53303524 AAAACTGCCGCTGAAGAGACTGGAGGAATCATAAGATAGTCTTCGAATCACAGAACAGAATCTCC AAAACTGCCGCTGAAGAGACTGGAGGAATCAT_AGATAGTCTTCGAATCACAGAACAGAATCTCC TA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53303521..53303597 26863196 MeRIP-seq:(Medium) rs1457797965 Functional Loss DEL dbSNP153 33..33 33 - - - 101650 RMVar_ID_101650 Human_SNP_ID_13634726 m1A Human chr1 - 53328012 53328012 53328012 GCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGCAACCCCGGCGCCGCGGCAAGGACTCGG GCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCGGCGGCAACCCCGGCGCCGCGGCAAGGACTCGG T C LRP8 Ensembl:ENSG00000157193 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:53327926..53328037 26863410 MeRIP-seq:(Medium) rs1258742463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9318955,Human_RBP_ID_18415547 RMVar_hsa_circ_268781 101651 RMVar_ID_101651 Human_SNP_ID_13634746 m1A Human chr1 - 53328039 53328036 53328039 TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGC___GGCGGCGGCGGCGGCGGCGGGGGCAGCGGC CGCT C LRP8 Ensembl:ENSG00000157193 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:53327944..53328074;chr1:53327940..53328091 26863410 MeRIP-seq:(Medium) rs1250947282 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_101831,Human_RBP_ID_9318955,Human_RBP_ID_18415547 RMVar_hsa_circ_268781 101652 RMVar_ID_101652 Human_SNP_ID_13634747 m1A Human chr1 - 53328039 53328039 53328039 TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCTGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC T A LRP8 Ensembl:ENSG00000157193 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:53327944..53328074;chr1:53327940..53328091 26863410 MeRIP-seq:(Medium) rs1340241530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101831,Human_RBP_ID_9318955,Human_RBP_ID_18415547 RMVar_hsa_circ_268781 101653 RMVar_ID_101653 Human_SNP_ID_13634748 m1A Human chr1 - 53328039 53328039 53328039 TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC T C LRP8 Ensembl:ENSG00000157193 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:53327944..53328074;chr1:53327940..53328091 26863410 MeRIP-seq:(Medium) rs1340241530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101831,Human_RBP_ID_9318955,Human_RBP_ID_18415547 RMVar_hsa_circ_268781 101654 RMVar_ID_101654 Human_SNP_ID_13734025 m1A Human chr1 - 53737925 53737925 53737925 CAGGGTCACCGTGAGTGGCGGCGGCTGCGGGGACAGGGGCCCGCGGGACCTGCTAGCCCGGCCGC CAGGGTCACCGTGAGTGGCGGCGGCTGCGGGGGCAGGGGCCCGCGGGACCTGCTAGCCCGGCCGC T C GLIS1 Ensembl:ENSG00000174332 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53737877..53737982 26863196 MeRIP-seq:(Medium) rs1033337228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48514 101655 RMVar_ID_101655 Human_SNP_ID_13734419 m1A Human chr1 + 53739174 53739174 53739174 CGGCGCGCCTCCACTGGCGCAGCAGCCCCCGCAGCCGCCGCAGCCGCCGCCGCCGCCGCCGCGTC CGGCGCGCCTCCACTGGCGCAGCAGCCCCCGCGGCCGCCGCAGCCGCCGCCGCCGCCGCCGCGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53739109..53739180 26863196 MeRIP-seq:(Medium) rs920837778 Functional Loss SNV dbSNP153 33..33 33 - - - 101656 RMVar_ID_101656 Human_SNP_ID_13746122 m1A Human chr1 - 53791010 53790996 53791011 GGGTAGGAGGAGGATGGAGAGAAGTAGGTTAAAGGGTACAAATATACAGTTAGAAGGAATAAATC GGGTAGGAGGAGGATGGAGAGAAGTAGGTTA_______________CAGTTAGAAGGAATAAATC GTATATTTGTACCCTT G NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53790960..53791094 26863196 MeRIP-seq:(Medium) rs1269468288 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_741495,Human_RBP_ID_801048,Human_RBP_ID_2155482,Human_RBP_ID_9529132 RMVar_hsa_circ_267919,RMVar_hsa_circ_316291,RMVar_hsa_circ_348703,RMVar_hsa_circ_368678,RMVar_hsa_circ_51243,RMVar_hsa_circ_267413,RMVar_hsa_circ_133116,RMVar_hsa_circ_110440,RMVar_hsa_circ_298628,RMVar_hsa_circ_336979,RMVar_hsa_circ_374648,RMVar_hsa_circ_378317,RMVar_hsa_circ_367210,RMVar_hsa_circ_313906,RMVar_hsa_circ_319478,RMVar_hsa_circ_300114,RMVar_hsa_circ_284014,RMVar_hsa_circ_293906,RMVar_hsa_circ_133118,RMVar_hsa_circ_133119,RMVar_hsa_circ_133117,RMVar_hsa_circ_64466,RMVar_hsa_circ_133114,RMVar_hsa_circ_133115,RMVar_hsa_circ_317756,RMVar_hsa_circ_133113,RMVar_hsa_circ_342341,RMVar_hsa_circ_310051,RMVar_hsa_circ_133122,RMVar_hsa_circ_49054,RMVar_hsa_circ_133121 101657 RMVar_ID_101657 Human_SNP_ID_13747391 m1A Human chr1 - 53795961 53795961 53795961 ACCAGTGTGGCTGGAGCAGAGTGAGTGAGGGGAGAGTGGTAAGTGGGTGATAAGATCAGAAAGGT ACCAGTGTGGCTGGAGCAGAGTGAGTGAGGGGGGAGTGGTAAGTGGGTGATAAGATCAGAAAGGT T C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:53795912..53796083 26863196 MeRIP-seq:(Medium) rs1267853782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23402814 RMVar_hsa_circ_2040,RMVar_hsa_circ_267919,RMVar_hsa_circ_348703,RMVar_hsa_circ_368678,RMVar_hsa_circ_51243,RMVar_hsa_circ_267413,RMVar_hsa_circ_133116,RMVar_hsa_circ_110440,RMVar_hsa_circ_336979,RMVar_hsa_circ_374648,RMVar_hsa_circ_378317,RMVar_hsa_circ_367210,RMVar_hsa_circ_313906,RMVar_hsa_circ_319478,RMVar_hsa_circ_300114,RMVar_hsa_circ_284014,RMVar_hsa_circ_293906,RMVar_hsa_circ_133118,RMVar_hsa_circ_133119,RMVar_hsa_circ_133117,RMVar_hsa_circ_64466,RMVar_hsa_circ_133114,RMVar_hsa_circ_133115,RMVar_hsa_circ_317756,RMVar_hsa_circ_133113,RMVar_hsa_circ_342341,RMVar_hsa_circ_310051,RMVar_hsa_circ_295508,RMVar_hsa_circ_133122,RMVar_hsa_circ_49054,RMVar_hsa_circ_308145,RMVar_hsa_circ_133121,RMVar_hsa_circ_301391,RMVar_hsa_circ_26248,RMVar_hsa_circ_269689,RMVar_hsa_circ_8294,RMVar_hsa_circ_133123 101658 RMVar_ID_101658 Human_SNP_ID_13757474 m1A Human chr1 - 53838014 53838014 53838014 GGGAAGTCCTGAGTGGAAGTTGGTTACGGGGTAGGAGAGGGGTCCTGAGTGGAAGGAAGCTGGTC GGGAAGTCCTGAGTGGAAGTTGGTTACGGGGTGGGAGAGGGGTCCTGAGTGGAAGGAAGCTGGTC T C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:53837966..53838046;chr1:53837807..53838173 26863196 MeRIP-seq:(Medium) rs1230565780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328458,Human_RBP_ID_5331685,Human_RBP_ID_5841920,Human_RBP_ID_23402896 RMVar_hsa_circ_110440,RMVar_hsa_circ_133113 101659 RMVar_ID_101659 Human_SNP_ID_13761070 m1A Human chr1 - 53852024 53852024 53852024 TTGCGAGCATGCGCTGATTGGACTGAAATGCCAGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC TTGCGAGCATGCGCTGATTGGACTGAAATGCCTGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC T A YIPF1 Ensembl:ENSG00000058799 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1127922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26381515 101660 RMVar_ID_101660 Human_SNP_ID_13761071 m1A Human chr1 - 53852024 53852024 53852024 TTGCGAGCATGCGCTGATTGGACTGAAATGCCAGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC TTGCGAGCATGCGCTGATTGGACTGAAATGCCGGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC T C YIPF1 Ensembl:ENSG00000058799 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1127922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26381515 101661 RMVar_ID_101661 Human_SNP_ID_13761072 m1A Human chr1 - 53852024 53852024 53852024 TTGCGAGCATGCGCTGATTGGACTGAAATGCCAGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC TTGCGAGCATGCGCTGATTGGACTGAAATGCCCGGGAATAGGTTAGGCATGCTCAGTGCCGTCCC T G YIPF1 Ensembl:ENSG00000058799 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1127922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26381515 101662 RMVar_ID_101662 Human_SNP_ID_13771096 m1A Human chr1 - 53895989 53895989 53895989 AAGCAGCAGTGTCCAAGGAGAGGTGCAGACAGAGAGCCATGAGCCGAAGGGAGAGAGCACATGCC AAGCAGCAGTGTCCAAGGAGAGGTGCAGACAGGGAGCCATGAGCCGAAGGGAGAGAGCACATGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:53895939..53896026 26863196 MeRIP-seq:(Medium) rs966317459 Functional Loss SNV dbSNP153 33..33 33 - - - 101663 RMVar_ID_101663 Human_SNP_ID_13781433 m1A Human chr1 + 53940060 53940060 53940060 TAGCTAAAATCACTTCGGACCCTTCAGAGCTCAGACAGAGATCAATTTTTCTCATCTTAAAGTGT TAGCTAAAATCACTTCGGACCCTTCAGAGCTCGGACAGAGATCAATTTTTCTCATCTTAAAGTGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:53940001..53940100 32194978 MeRIP-seq:(Medium) rs1309898266 Functional Loss SNV dbSNP153 33..33 33 - - - 101664 RMVar_ID_101664 Human_SNP_ID_13781440 m1A Human chr1 + 53940072 53940072 53940072 CTTCGGACCCTTCAGAGCTCAGACAGAGATCAATTTTTCTCATCTTAAAGTGTTTAACCTGCAAA CTTCGGACCCTTCAGAGCTCAGACAGAGATCAGTTTTTCTCATCTTAAAGTGTTTAACCTGCAAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:53940026..53940100 26863196 MeRIP-seq:(Medium) rs200095391 Functional Loss SNV dbSNP153 33..33 33 - - - 101665 RMVar_ID_101665 Human_SNP_ID_13782827 m1A Human chr1 - 53945587 53945587 53945587 GGGCGGGGCGCAAGGGAGGTTTCGAGCCCGGAAGGTCCGGCGCCCAGAGCTAACGGGAGTCCCAG GGGCGGGGCGCAAGGGAGGTTTCGAGCCCGGACGGTCCGGCGCCCAGAGCTAACGGGAGTCCCAG T G HSPB11 Ensembl:ENSG00000081870 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:53945551..53945675 32194978 MeRIP-seq:(Medium) rs1050712704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221203,Human_RBP_ID_4059846,Human_RBP_ID_5311727,Human_RBP_ID_18414968,Human_RBP_ID_23402957 Human_Splice_Rec_73315,Human_Splice_Rec_73325,Human_Splice_Rec_73339,Human_Splice_Rec_73349 Human_miRNA_ID_2422899,Human_miRNA_ID_2432552 RMVar_hsa_circ_133157,RMVar_hsa_circ_117783 101666 RMVar_ID_101666 Human_SNP_ID_13782833 m1A Human chr1 - 53945603 53945603 53945603 CGGGACGCTCTGCGTGGGGCGGGGCGCAAGGGAGGTTTCGAGCCCGGAAGGTCCGGCGCCCAGAG CGGGACGCTCTGCGTGGGGCGGGGCGCAAGGGCGGTTTCGAGCCCGGAAGGTCCGGCGCCCAGAG T G HSPB11 Ensembl:ENSG00000081870 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53940046..53945879 26863196 MeRIP-seq:(Medium) rs1261291875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4059847,Human_RBP_ID_5311727,Human_RBP_ID_18414968 Human_Splice_Rec_73315,Human_Splice_Rec_73325,Human_Splice_Rec_73339,Human_Splice_Rec_73349 RMVar_hsa_circ_133157,RMVar_hsa_circ_117783 101667 RMVar_ID_101667 Human_SNP_ID_13782861 m1A Human chr1 + 53945672 53945672 53945672 GCAGCTCCGCCTGCTCGCCGCGGCCTCCGTGGAGTCCGGGGTCGCGCGCGCTCCAACTCTGAAAT GCAGCTCCGCCTGCTCGCCGCGGCCTCCGTGGCGTCCGGGGTCGCGCGCGCTCCAACTCTGAAAT A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:53945593..53945678 26863410 MeRIP-seq:(Medium) rs925379522 Functional Loss SNV dbSNP153 33..33 33 - - - 101668 RMVar_ID_101668 Human_SNP_ID_13783238 m1A Human chr1 - 53946451 53946451 53946451 CTGACGGGGAAGGGCTCAGCACCCCGGGCACAAAGCTAGGAAGGGTGGGACACAGTGAAGGTGGG CTGACGGGGAAGGGCTCAGCACCCCGGGCACAGAGCTAGGAAGGGTGGGACACAGTGAAGGTGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:53946426..53946450 26863196 MeRIP-seq:(Medium) rs982442684 Functional Loss SNV dbSNP153 33..33 33 - - - 101669 RMVar_ID_101669 Human_SNP_ID_13783261 m1A Human chr1 - 53946508 53946508 53946508 TGCCCGGGGCAGCGAGCGGCAGCTCCTCGGTGACGGCTCCCTCCTCCCGCGGCCCGGCTGACGGG TGCCCGGGGCAGCGAGCGGCAGCTCCTCGGTGGCGGCTCCCTCCTCCCGCGGCCCGGCTGACGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:53946351..53947807 26863196 MeRIP-seq:(Medium) rs1063162 Functional Loss SNV dbSNP153 33..33 33 - - - 101670 RMVar_ID_101670 Human_SNP_ID_13783268 m1A Human chr1 - 53946526 53946526 53946526 GCCACCTACCTGTGCCCCTGCCCGGGGCAGCGAGCGGCAGCTCCTCGGTGACGGCTCCCTCCTCC GCCACCTACCTGTGCCCCTGCCCGGGGCAGCGGGCGGCAGCTCCTCGGTGACGGCTCCCTCCTCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:53946125..53947896 26863410 MeRIP-seq:(Medium) rs1185198744 Functional Loss SNV dbSNP153 33..33 33 - - - 101671 RMVar_ID_101671 Human_SNP_ID_13783269 m1A Human chr1 - 53946526 53946526 53946526 GCCACCTACCTGTGCCCCTGCCCGGGGCAGCGAGCGGCAGCTCCTCGGTGACGGCTCCCTCCTCC GCCACCTACCTGTGCCCCTGCCCGGGGCAGCGCGCGGCAGCTCCTCGGTGACGGCTCCCTCCTCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:53946125..53947896 26863410 MeRIP-seq:(Medium) rs1185198744 Functional Loss SNV dbSNP153 33..33 33 - - - 101672 RMVar_ID_101672 Human_SNP_ID_13790341 m1A Human chr1 + 53975279 53975279 53975279 CCCTCTACTACTATAACCAGGACCGCCGCCATAGTTGCCACCATCACCTCCAAATCCATTATATC CCCTCTACTACTATAACCAGGACCGCCGCCATGGTTGCCACCATCACCTCCAAATCCATTATATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:53975203..53975352 26863196 MeRIP-seq:(Medium) rs1485287161 Functional Loss SNV dbSNP153 33..33 33 - - - 101673 RMVar_ID_101673 Human_SNP_ID_13809287 m1A Human chr1 + 54053047 54053047 54053047 CAAGGGGTAGGTCAACTGACAGGCCCGGTGGCAAGACGCCGTATCACCCAAGACCGAGTCAAATG CAAGGGGTAGGTCAACTGACAGGCCCGGTGGCGAGACGCCGTATCACCCAAGACCGAGTCAAATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:54053001..54053075 32194978 MeRIP-seq:(Medium) rs532070089 Functional Loss SNV dbSNP153 33..33 33 - - - 101674 RMVar_ID_101674 Human_SNP_ID_13809339 m1A Human chr1 - 54053150 54053150 54053150 GCGCCGAAGGGGAGCCTCTGGGTGAGGACCCAACTGGGGCTCCCGCCGCTGCTGCTGCTGACCAT GCGCCGAAGGGGAGCCTCTGGGTGAGGACCCAGCTGGGGCTCCCGCCGCTGCTGCTGCTGACCAT T C TMEM59 Ensembl:ENSG00000116209 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:54053126..54053150 26863196 MeRIP-seq:(Medium) rs764707352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221308,Human_RBP_ID_358362,Human_RBP_ID_802586,Human_RBP_ID_3933579,Human_RBP_ID_4072834,Human_RBP_ID_9318958,Human_RBP_ID_18468579,Human_RBP_ID_22427272,Human_RBP_ID_23403040 Human_miRNA_ID_2755956 RMVar_hsa_circ_75634,RMVar_hsa_circ_133173 101675 RMVar_ID_101675 Human_SNP_ID_13809428 m1A Human chr1 + 54053363 54053363 54053363 CAGAAACTGCCGCCTCCTGCCTCACCTCTGGGACTACGAACTTCTTCTCCTAGGCTGGCGTGAGG CAGAAACTGCCGCCTCCTGCCTCACCTCTGGGCCTACGAACTTCTTCTCCTAGGCTGGCGTGAGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:54053267..54053399 26863196 MeRIP-seq:(Medium) rs1469954428 Functional Loss SNV dbSNP153 33..33 33 - - - 101676 RMVar_ID_101676 Human_SNP_ID_13844193 m1A Human chr1 + 54200236 54200236 54200236 GGCGGGGTCCAGGTGGAGGTCTTGAGGCTATCAGATCGGTATGGCATTGGCGTCCGGGCCCGCAA GGCGGGGTCCAGGTGGAGGTCTTGAGGCTATCTGATCGGTATGGCATTGGCGTCCGGGCCCGCAA A T MRPL37 Ensembl:ENSG00000116221 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:54200176..54200350 26863196 MeRIP-seq:(Medium) rs1235005901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358457,Human_RBP_ID_4060087,Human_RBP_ID_8314900,Human_RBP_ID_11037628,Human_RBP_ID_22428388,Human_RBP_ID_23403138 Human_Splice_Rec_73733 RMVar_hsa_circ_104422,RMVar_hsa_circ_133179,RMVar_hsa_circ_88402,RMVar_hsa_circ_133178 101677 RMVar_ID_101677 Human_SNP_ID_13844207 m1A Human chr1 - 54200250 54200250 54200250 AGCTAGCGCCCGCCTTGCGGGCCCGGACGCCAATGCCATACCGATCTGATAGCCTCAAGACCTCC AGCTAGCGCCCGCCTTGCGGGCCCGGACGCCAGTGCCATACCGATCTGATAGCCTCAAGACCTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:54200201..54200350 26863196 MeRIP-seq:(Medium) rs749134167 Functional Loss SNV dbSNP153 33..33 33 - - - 101678 RMVar_ID_101678 Human_SNP_ID_13844208 m1A Human chr1 - 54200251 54200251 54200251 CAGCTAGCGCCCGCCTTGCGGGCCCGGACGCCAATGCCATACCGATCTGATAGCCTCAAGACCTC CAGCTAGCGCCCGCCTTGCGGGCCCGGACGCCGATGCCATACCGATCTGATAGCCTCAAGACCTC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:54200201..54200375 26863196 MeRIP-seq:(Medium) rs768838597 Functional Loss SNV dbSNP153 33..33 33 - - - 101679 RMVar_ID_101679 Human_SNP_ID_13844236 m1A Human chr1 - 54200302 54200302 54200302 ACGCCCCGCGTCTCGGGGCCCCGAAGCCCCCAAGGCCGAGCTGCCCGGAGCCAGCTAGCGCCCGC ACGCCCCGCGTCTCGGGGCCCCGAAGCCCCCAGGGCCGAGCTGCCCGGAGCCAGCTAGCGCCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:54200201..54200575 26863410 MeRIP-seq:(Medium) rs11544812 Functional Loss SNV dbSNP153 33..33 33 - - - 101680 RMVar_ID_101680 Human_SNP_ID_13844237 m1A Human chr1 - 54200302 54200302 54200302 ACGCCCCGCGTCTCGGGGCCCCGAAGCCCCCAAGGCCGAGCTGCCCGGAGCCAGCTAGCGCCCGC ACGCCCCGCGTCTCGGGGCCCCGAAGCCCCCACGGCCGAGCTGCCCGGAGCCAGCTAGCGCCCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:54200201..54200575 26863410 MeRIP-seq:(Medium) rs11544812 Functional Loss SNV dbSNP153 33..33 33 - - - 101681 RMVar_ID_101681 Human_SNP_ID_13844284 m1A Human chr1 + 54200397 54200397 54200397 CGGAGCCTCCTCCCCTGGATAGGGTGTACGAGATCCCTGGACTGGAGCCCATCACCTTTGCGGGG CGGAGCCTCCTCCCCTGGATAGGGTGTACGAGGTCCCTGGACTGGAGCCCATCACCTTTGCGGGG A G MRPL37 Ensembl:ENSG00000116221 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:54200201..54200425 26863196 MeRIP-seq:(Medium) rs534430418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358461,Human_RBP_ID_1432805,Human_RBP_ID_4074077,Human_RBP_ID_5162278,Human_RBP_ID_5842348,Human_RBP_ID_8753985,Human_RBP_ID_11037629,Human_RBP_ID_22429393,Human_RBP_ID_23403140,Human_RBP_ID_27184944 Human_miRNA_ID_2655913 RMVar_hsa_circ_104422,RMVar_hsa_circ_133179,RMVar_hsa_circ_88402,RMVar_hsa_circ_133178 101682 RMVar_ID_101682 Human_SNP_ID_13845333 m1A Human chr1 - 54204992 54204989 54204993 TTTACACCTTTGAGGTAATTAGCCACAAAAATAAAGAAGGAAAGAAAAAGATTCAGGAAGAGATG TTTACACCTTTGAGGTAATTAGCCACAAAAA____GAAGGAAAGAAAAAGATTCAGGAAGAGATG CTTTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:54204990..54205096 26863196 MeRIP-seq:(Medium) rs1177424608 Functional Loss DEL dbSNP153 32..35 33 - - - 101683 RMVar_ID_101683 Human_SNP_ID_13845409 m1A Human chr1 + 54205186 54205184 54205186 CCGTCTCTGGCAGACCACTGAGGAAATCCCCAAGAGAGAGACCTACTGGTAAGTTCCCCCAAGTA CCGTCTCTGGCAGACCACTGAGGAAATCCCC__GAGAGAGACCTACTGGTAAGTTCCCCCAAGTA CAA C MRPL37 Ensembl:ENSG00000116221 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:54204981..54205382 26863196 MeRIP-seq:(Medium) rs752853617 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9271418,Human_RBP_ID_18187142,Human_RBP_ID_19038318,Human_RBP_ID_26798468 Human_Splice_Rec_73697,Human_Splice_Rec_73711,Human_Splice_Rec_73723,Human_Splice_Rec_73735 RMVar_hsa_circ_21246,RMVar_hsa_circ_104422,RMVar_hsa_circ_133179,RMVar_hsa_circ_88402,RMVar_hsa_circ_315052,RMVar_hsa_circ_319989,RMVar_hsa_circ_133178,RMVar_hsa_circ_319699,RMVar_hsa_circ_280492,RMVar_hsa_circ_133180,RMVar_hsa_circ_133181 101684 RMVar_ID_101684 Human_SNP_ID_13845411 m1A Human chr1 + 54205186 54205186 54205186 CCGTCTCTGGCAGACCACTGAGGAAATCCCCAAGAGAGAGACCTACTGGTAAGTTCCCCCAAGTA CCGTCTCTGGCAGACCACTGAGGAAATCCCCAGGAGAGAGACCTACTGGTAAGTTCCCCCAAGTA A G MRPL37 Ensembl:ENSG00000116221 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:54204981..54205382 26863196 MeRIP-seq:(Medium) rs1360289263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9271418,Human_RBP_ID_18187142,Human_RBP_ID_19038318,Human_RBP_ID_26798468 Human_Splice_Rec_73697,Human_Splice_Rec_73711,Human_Splice_Rec_73723,Human_Splice_Rec_73735 RMVar_hsa_circ_21246,RMVar_hsa_circ_104422,RMVar_hsa_circ_133179,RMVar_hsa_circ_88402,RMVar_hsa_circ_315052,RMVar_hsa_circ_319989,RMVar_hsa_circ_133178,RMVar_hsa_circ_319699,RMVar_hsa_circ_280492,RMVar_hsa_circ_133180,RMVar_hsa_circ_133181 101685 RMVar_ID_101685 Human_SNP_ID_13850911 m1A Human chr1 - 54226267 54226267 54226267 CACAGCCCAGACCGTCACCGTGACCCGGTGGCATGCACTGTTCCCAGGACACCCTCCTCCTCTCC CACAGCCCAGACCGTCACCGTGACCCGGTGGCGTGCACTGTTCCCAGGACACCCTCCTCCTCTCC T C SSBP3 Ensembl:ENSG00000157216 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:54226219..54226313 26863196 MeRIP-seq:(Medium) rs1557431708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358538,Human_RBP_ID_8168064 101686 RMVar_ID_101686 Human_SNP_ID_13856372 m1A Human chr1 - 54242100 54242100 54242100 GTCAGGGGAGCGGTTCTGGGTGCAGGGGAGCTACTGTCCCTGGGTGTAGGTGTCACGGGAAGTGG GTCAGGGGAGCGGTTCTGGGTGCAGGGGAGCTGCTGTCCCTGGGTGTAGGTGTCACGGGAAGTGG T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54242054..54242149 26863196 MeRIP-seq:(Medium) rs1366012267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_850072,Human_RBP_ID_5311730,Human_RBP_ID_5331697,Human_RBP_ID_19041452,Human_RBP_ID_22637055,Human_RBP_ID_26773390,Human_RBP_ID_27835230 RMVar_hsa_circ_5296,RMVar_hsa_circ_29296,RMVar_hsa_circ_349836,RMVar_hsa_circ_368793,RMVar_hsa_circ_31377,RMVar_hsa_circ_133188,RMVar_hsa_circ_133190,RMVar_hsa_circ_282423,RMVar_hsa_circ_53237 101687 RMVar_ID_101687 Human_SNP_ID_13857182 m1A Human chr1 + 54244780 54244780 54244780 TTCCCTGCTCCCTGCTTGGCAGGCTCCTACTCAGCTCCAAGAGCAGCTCCTCTAGGAAGCCCTCC TTCCCTGCTCCCTGCTTGGCAGGCTCCTACTCGGCTCCAAGAGCAGCTCCTCTAGGAAGCCCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54244763..54244912 26863196 MeRIP-seq:(Medium) rs1014895340 Functional Loss SNV dbSNP153 33..33 33 - - - 101688 RMVar_ID_101688 Human_SNP_ID_13860958 m1A Human chr1 - 54257998 54257998 54257998 GGGCGCGGAGGAAGCAGAGAGCCCGCAGAGGAAAAACAAAAATCAAAATGTGCTCTAGCCACTGC GGGCGCGGAGGAAGCAGAGAGCCCGCAGAGGAGAAACAAAAATCAAAATGTGCTCTAGCCACTGC T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:54257996..54258079 26863196 MeRIP-seq:(Medium) rs1157544713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5296,RMVar_hsa_circ_133194,RMVar_hsa_circ_312718,RMVar_hsa_circ_369683,RMVar_hsa_circ_29388,RMVar_hsa_circ_133193 101689 RMVar_ID_101689 Human_SNP_ID_13865477 m1A Human chr1 + 54274823 54274823 54274823 GCTCTCCCCAACTTTAAGTCCTTCCTGTGTCTATTCCTGGCTCCATCCCCACACCCCAGCCTGCA GCTCTCCCCAACTTTAAGTCCTTCCTGTGTCTGTTCCTGGCTCCATCCCCACACCCCAGCCTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:54274819..54275033 26863196 MeRIP-seq:(Medium) rs1007599901 Functional Loss SNV dbSNP153 33..33 33 - - - 101690 RMVar_ID_101690 Human_SNP_ID_13901638 m1A Human chr1 + 54406062 54406060 54406062 CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGC__CCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC CTA C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:54405975..54406066;chr1:54405989..54406090 26863410 MeRIP-seq:(Medium) rs1217258488 Functional Loss DEL dbSNP153 32..33 33 - - - 101691 RMVar_ID_101691 Human_SNP_ID_13901640 m1A Human chr1 + 54406062 54406062 54406062 CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGCTGCCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:54405975..54406066;chr1:54405989..54406090 26863410 MeRIP-seq:(Medium) rs1435546926 Functional Loss SNV dbSNP153 33..33 33 - - - 101692 RMVar_ID_101692 Human_SNP_ID_13901746 m1A Human chr1 + 54406287 54406287 54406287 CTCGGCCTGGGGGTGCCGCCGCCGCCGCCCGCACGGCCGCCCGCTCTCCGCTCGCTCGCGCGCCC CTCGGCCTGGGGGTGCCGCCGCCGCCGCCCGCGCGGCCGCCCGCTCTCCGCTCGCTCGCGCGCCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:54405985..54406400 26863196 MeRIP-seq:(Medium) rs1182458353 Functional Loss SNV dbSNP153 33..33 33 - - - 101693 RMVar_ID_101693 Human_SNP_ID_13901770 m1A Human chr1 - 54406327 54406327 54406327 GGTGCTGGAGGCGCAGAGGGCGGCGCAGGCGGAGCCGGGCGGGCGCGCGAGCGAGCGGAGAGCGG GGTGCTGGAGGCGCAGAGGGCGGCGCAGGCGGGGCCGGGCGGGCGCGCGAGCGAGCGGAGAGCGG T C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr1:54406226..54406400;chr1:54406251..54406425 26863410 MeRIP-seq:(Medium) rs1381679521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3330338,Human_RBP_ID_4074081,Human_RBP_ID_9318967,Human_RBP_ID_17668075,Human_RBP_ID_18187147 101694 RMVar_ID_101694 Human_SNP_ID_13901782 m1A Human chr1 - 54406351 54406351 54406351 GGCGGCGGCGGCGGCGGCGGCAGCGGTGCTGGAGGCGCAGAGGGCGGCGCAGGCGGAGCCGGGCG GGCGGCGGCGGCGGCGGCGGCAGCGGTGCTGGGGGCGCAGAGGGCGGCGCAGGCGGAGCCGGGCG T C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:54406251..54406375 26863410 MeRIP-seq:(Medium) rs914251491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074081,Human_RBP_ID_9318968,Human_RBP_ID_17668075 101695 RMVar_ID_101695 Human_SNP_ID_13901783 m1A Human chr1 - 54406351 54406351 54406351 GGCGGCGGCGGCGGCGGCGGCAGCGGTGCTGGAGGCGCAGAGGGCGGCGCAGGCGGAGCCGGGCG GGCGGCGGCGGCGGCGGCGGCAGCGGTGCTGGCGGCGCAGAGGGCGGCGCAGGCGGAGCCGGGCG T G SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:54406251..54406375 26863410 MeRIP-seq:(Medium) rs914251491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074081,Human_RBP_ID_9318968,Human_RBP_ID_17668075 101696 RMVar_ID_101696 Human_SNP_ID_13901806 m1A Human chr1 - 54406389 54406374 54406389 GTAGCCACGTTCGGTTGAGCTCCAAGTAGACCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGT GTAGCCACGTTCGGTTGAGCTCCAAGTAGACC_______________GGCGGCGGCGGCAGCGGT CGCCGCCGCCGCCGCT C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:54406288..54406388 26863410 MeRIP-seq:(Medium) rs1002685594 Functional Loss DEL dbSNP153 33..47 33 - - - 101697 RMVar_ID_101697 Human_SNP_ID_13901808 m1A Human chr1 - 54406389 54406383 54406389 GTAGCCACGTTCGGTTGAGCTCCAAGTAGACCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGT GTAGCCACGTTCGGTTGAGCTCCAAGTAGACC______GGCGGCGGCGGCGGCGGCGGCAGCGGT CGCCGCT C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:54406288..54406388 26863410 MeRIP-seq:(Medium) rs1475306559 Functional Loss DEL dbSNP153 33..38 33 - - - 101698 RMVar_ID_101698 Human_SNP_ID_13901811 m1A Human chr1 - 54406389 54406386 54406389 GTAGCCACGTTCGGTTGAGCTCCAAGTAGACCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGT GTAGCCACGTTCGGTTGAGCTCCAAGTAGACC___GGCGGCGGCGGCGGCGGCGGCGGCAGCGGT CGCT C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:54406288..54406388 26863410 MeRIP-seq:(Medium) rs1421135678 Functional Loss DEL dbSNP153 33..35 33 - - - 101699 RMVar_ID_101699 Human_SNP_ID_13901812 m1A Human chr1 - 54406389 54406389 54406389 GTAGCCACGTTCGGTTGAGCTCCAAGTAGACCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGT GTAGCCACGTTCGGTTGAGCTCCAAGTAGACCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGT T C SSBP3 Ensembl:ENSG00000157216 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:54406288..54406388 26863410 MeRIP-seq:(Medium) rs529788881 Functional Loss SNV dbSNP153 33..33 33 - - - 101700 RMVar_ID_101700 Human_SNP_ID_13983894 m1A Human chr1 - 54715920 54715920 54715920 TCCATGACGTCGTCTGAGGTGGGATCCTGCCCAGGTTGTTCCATAGCTGATGCCCTGCCTTCCAG TCCATGACGTCGTCTGAGGTGGGATCCTGCCCCGGTTGTTCCATAGCTGATGCCCTGCCTTCCAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54715871..54715973 26863196 MeRIP-seq:(Medium) rs1456068418 Functional Loss SNV dbSNP153 33..33 33 - - - 101701 RMVar_ID_101701 Human_SNP_ID_13990221 m1A Human chr1 + 54741702 54741702 54741702 TCCCTAAACTGCAGCCTCTCTGGCTGGTCTTCACTTTCCTCAGTTGATATAAAACTCTGGGTCTT TCCCTAAACTGCAGCCTCTCTGGCTGGTCTTCGCTTTCCTCAGTTGATATAAAACTCTGGGTCTT A G TTC4,MROH7-TTC4 Ensembl:ENSG00000243725,Ensembl:ENSG00000271723 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:54741558..54742011 32194978 MeRIP-seq:(Medium) rs530019461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1432820,Human_RBP_ID_17754591 Human_miRNA_ID_53338,Human_miRNA_ID_53339,Human_miRNA_ID_60900,Human_miRNA_ID_60901,Human_miRNA_ID_383661,Human_miRNA_ID_383662,Human_miRNA_ID_560162,Human_miRNA_ID_560163,Human_miRNA_ID_567665,Human_miRNA_ID_567666,Human_miRNA_ID_1585668,Human_miRNA_ID_1585669 101702 RMVar_ID_101702 Human_SNP_ID_14017255 m1A Human chr1 + 54850827 54850827 54850827 GTCTTGTCTGTAGCGATGTGACAGATGAGGAAACTGCAGCTCAGAGGACAATGACTTGCCCACGT GTCTTGTCTGTAGCGATGTGACAGATGAGGAATCTGCAGCTCAGAGGACAATGACTTGCCCACGT A T HSALNG0003805 RNACentral:URS0000E9CC4B lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:54850776..54850975 32194978 MeRIP-seq:(Medium) rs113491597 Functional Loss SNV dbSNP153 33..33 33 - - - 101703 RMVar_ID_101703 Human_SNP_ID_14017654 m1A Human chr1 - 54852372 54852372 54852372 ACTTCTCTGCCTCTGCAGCTTCCAGATGCTGTATGCCGACTGCTACATGAACCGGGAGGAGTTCT ACTTCTCTGCCTCTGCAGCTTCCAGATGCTGTCTGCCGACTGCTACATGAACCGGGAGGAGTTCT T G DHCR24 Ensembl:ENSG00000116133 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:54852142..54852407 26863196 MeRIP-seq:(Medium) rs28939092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_979128,Human_RBP_ID_1750795,Human_RBP_ID_8315093,Human_RBP_ID_11040070,Human_RBP_ID_22427279,Human_RBP_ID_22749184,Human_RBP_ID_27400122 Human_Splice_Rec_74936,Human_Splice_Rec_74954,Human_Splice_Rec_74972,Human_Splice_Rec_75006,Human_Splice_Rec_75024,Human_Splice_Rec_75040,Human_Splice_Rec_75058 Clinvar_Rec_622 GWAS_ID_13380 RMVar_hsa_circ_78694,RMVar_hsa_circ_133210 101704 RMVar_ID_101704 Human_SNP_ID_14019527 m1A Human chr1 - 54860112 54860112 54860112 TTGGTCAGTTCTGACATTGGGCAAGTATCTTAAGCAGAATGTGATTGGGCGGTGGTAGGGGTGGA TTGGTCAGTTCTGACATTGGGCAAGTATCTTAGGCAGAATGTGATTGGGCGGTGGTAGGGGTGGA T C DHCR24 Ensembl:ENSG00000116133 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:54860110..54860524 26863196 MeRIP-seq:(Medium) rs1557431703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126930,RMVar_hsa_circ_78694,RMVar_hsa_circ_133210,RMVar_hsa_circ_133213,RMVar_hsa_circ_115286,RMVar_hsa_circ_121032,RMVar_hsa_circ_133211,RMVar_hsa_circ_133214 101705 RMVar_ID_101705 Human_SNP_ID_14019532 m1A Human chr1 - 54860153 54860153 54860153 CATGACGGAATTATACCTGGTGGGCTTCTAGGAGAGGGTGATTGGTCAGTTCTGACATTGGGCAA CATGACGGAATTATACCTGGTGGGCTTCTAGGTGAGGGTGATTGGTCAGTTCTGACATTGGGCAA T A DHCR24 Ensembl:ENSG00000116133 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54860151..54860371 26863196 MeRIP-seq:(Medium) rs972994610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126930,RMVar_hsa_circ_78694,RMVar_hsa_circ_133210,RMVar_hsa_circ_133213,RMVar_hsa_circ_115286,RMVar_hsa_circ_121032,RMVar_hsa_circ_133211,RMVar_hsa_circ_133214 101706 RMVar_ID_101706 Human_SNP_ID_14019533 m1A Human chr1 - 54860153 54860153 54860153 CATGACGGAATTATACCTGGTGGGCTTCTAGGAGAGGGTGATTGGTCAGTTCTGACATTGGGCAA CATGACGGAATTATACCTGGTGGGCTTCTAGGCGAGGGTGATTGGTCAGTTCTGACATTGGGCAA T G DHCR24 Ensembl:ENSG00000116133 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54860151..54860371 26863196 MeRIP-seq:(Medium) rs972994610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126930,RMVar_hsa_circ_78694,RMVar_hsa_circ_133210,RMVar_hsa_circ_133213,RMVar_hsa_circ_115286,RMVar_hsa_circ_121032,RMVar_hsa_circ_133211,RMVar_hsa_circ_133214 101707 RMVar_ID_101707 Human_SNP_ID_14023273 m1A Human chr1 - 54875990 54875990 54875990 CCATGGGCCAGGTGACTGCCCTGCTGACCTCCATTGGCTGGACTCTCCCCGTGTTGCCTGAGCTT CCATGGGCCAGGTGACTGCCCTGCTGACCTCCGTTGGCTGGACTCTCCCCGTGTTGCCTGAGCTT T C DHCR24 Ensembl:ENSG00000116133 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:54875905..54875994 26863196 MeRIP-seq:(Medium) rs141061353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1155280,Human_RBP_ID_4097889,Human_RBP_ID_8315106,Human_RBP_ID_11040257,Human_RBP_ID_22145344,Human_RBP_ID_22428399,Human_RBP_ID_22785392,Human_RBP_ID_23403632 Human_Splice_Rec_74924,Human_Splice_Rec_74925,Human_Splice_Rec_74942,Human_Splice_Rec_74943,Human_Splice_Rec_74958,Human_Splice_Rec_74959,Human_Splice_Rec_74978,Human_Splice_Rec_74979,Human_Splice_Rec_74994,Human_Splice_Rec_74995,Human_Splice_Rec_75012,Human_Splice_Rec_75013,Human_Splice_Rec_75028,Human_Splice_Rec_75029,Human_Splice_Rec_75046,Human_Splice_Rec_75047,Human_Splice_Rec_75062,Human_Splice_Rec_75063,Human_Splice_Rec_75070,Human_Splice_Rec_75071,Human_Splice_Rec_75078,Human_Splice_Rec_75079,Human_Splice_Rec_75088 Human_miRNA_ID_2972101,Human_miRNA_ID_3005284 RMVar_hsa_circ_133218,RMVar_hsa_circ_313574,RMVar_hsa_circ_366799,RMVar_hsa_circ_133215,RMVar_hsa_circ_326278,RMVar_hsa_circ_275585,RMVar_hsa_circ_133216,RMVar_hsa_circ_127316,RMVar_hsa_circ_133220,RMVar_hsa_circ_104165,RMVar_hsa_circ_133219,RMVar_hsa_circ_77842,RMVar_hsa_circ_133221 101708 RMVar_ID_101708 Human_SNP_ID_14023274 m1A Human chr1 - 54875990 54875990 54875990 CCATGGGCCAGGTGACTGCCCTGCTGACCTCCATTGGCTGGACTCTCCCCGTGTTGCCTGAGCTT CCATGGGCCAGGTGACTGCCCTGCTGACCTCCCTTGGCTGGACTCTCCCCGTGTTGCCTGAGCTT T G DHCR24 Ensembl:ENSG00000116133 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:54875905..54875994 26863196 MeRIP-seq:(Medium) rs141061353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1155280,Human_RBP_ID_4097889,Human_RBP_ID_8315106,Human_RBP_ID_11040257,Human_RBP_ID_22145344,Human_RBP_ID_22428399,Human_RBP_ID_22785392,Human_RBP_ID_23403632 Human_Splice_Rec_74924,Human_Splice_Rec_74925,Human_Splice_Rec_74942,Human_Splice_Rec_74943,Human_Splice_Rec_74958,Human_Splice_Rec_74959,Human_Splice_Rec_74978,Human_Splice_Rec_74979,Human_Splice_Rec_74994,Human_Splice_Rec_74995,Human_Splice_Rec_75012,Human_Splice_Rec_75013,Human_Splice_Rec_75028,Human_Splice_Rec_75029,Human_Splice_Rec_75046,Human_Splice_Rec_75047,Human_Splice_Rec_75062,Human_Splice_Rec_75063,Human_Splice_Rec_75070,Human_Splice_Rec_75071,Human_Splice_Rec_75078,Human_Splice_Rec_75079,Human_Splice_Rec_75088 Human_miRNA_ID_2972101,Human_miRNA_ID_3005284 RMVar_hsa_circ_133218,RMVar_hsa_circ_313574,RMVar_hsa_circ_366799,RMVar_hsa_circ_133215,RMVar_hsa_circ_326278,RMVar_hsa_circ_275585,RMVar_hsa_circ_133216,RMVar_hsa_circ_127316,RMVar_hsa_circ_133220,RMVar_hsa_circ_104165,RMVar_hsa_circ_133219,RMVar_hsa_circ_77842,RMVar_hsa_circ_133221 101709 RMVar_ID_101709 Human_SNP_ID_14025940 m1A Human chr1 - 54887158 54887158 54887158 GGGCCAGGCGCGGAGCTGGCGGCAGTGACAGGAGGCGCGAACCCGCAGCGCTTACCGCGCGGCGC GGGCCAGGCGCGGAGCTGGCGGCAGTGACAGGGGGCGCGAACCCGCAGCGCTTACCGCGCGGCGC T C DHCR24 Ensembl:ENSG00000116133 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:54886820..54887225 26863196 MeRIP-seq:(Medium) rs1313130673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803922,Human_RBP_ID_4072841,Human_RBP_ID_5278396,Human_RBP_ID_22428403,Human_RBP_ID_22563397 RMVar_hsa_circ_127316,RMVar_hsa_circ_133220 101710 RMVar_ID_101710 Human_SNP_ID_14064358 m1A Human chr1 - 55039601 55039601 55039601 TCTCACTGCCTGGCTCACTCCTCCAGGCTCAGACCCTGAACTGAACGGCGGCGCCCGCCTGCAAC TCTCACTGCCTGGCTCACTCCTCCAGGCTCAGCCCCTGAACTGAACGGCGGCGCCCGCCTGCAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:55039551..55039770 26863196 MeRIP-seq:(Medium) rs886046427 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_623 101711 RMVar_ID_101711 Human_SNP_ID_14064370 m1A Human chr1 + 55039627 55039627 55039627 TCAGGGTCTGAGCCTGGAGGAGTGAGCCAGGCAGTGAGACTGGCTCGGGCGGGCCGGGACGCGTC TCAGGGTCTGAGCCTGGAGGAGTGAGCCAGGCGGTGAGACTGGCTCGGGCGGGCCGGGACGCGTC A G PCSK9 Ensembl:ENSG00000169174 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:55039576..55039763 26863196 MeRIP-seq:(Medium) rs1351851735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25595,Human_RBP_ID_746033,Human_RBP_ID_4072842,Human_RBP_ID_5233985,Human_RBP_ID_8754998,Human_RBP_ID_9270160,Human_RBP_ID_9318971,Human_RBP_ID_18187150,Human_RBP_ID_22427280 101712 RMVar_ID_101712 Human_SNP_ID_14064448 m1A Human chr1 + 55039816 55039816 55039816 CGCGCACGGCCTCTAGGTCTCCTCGCCAGGACAGCAACCTCTCCCCTGGCCCTCATGGGCACCGT CGCGCACGGCCTCTAGGTCTCCTCGCCAGGACCGCAACCTCTCCCCTGGCCCTCATGGGCACCGT A C PCSK9 Ensembl:ENSG00000169174 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:55039801..55039825 26863196 MeRIP-seq:(Medium) rs1387827816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22428407 101713 RMVar_ID_101713 Human_SNP_ID_14064510 m1A Human chr1 - 55039905 55039905 55039905 CGTCCTCCTGCGCACGGGCGCCCGCGGGACCCAGGAGCAGCAGCAGCAGCAGCAGCAGTGGCAGC CGTCCTCCTGCGCACGGGCGCCCGCGGGACCCCGGAGCAGCAGCAGCAGCAGCAGCAGTGGCAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55039856..55040005 26863196 MeRIP-seq:(Medium) rs1557497443 Functional Loss SNV dbSNP153 33..33 33 - - - 101714 RMVar_ID_101714 Human_SNP_ID_14067886 m1A Human chr1 - 55052747 55052746 55052747 CGCTAACCGTGCCCTTCCCTTGGCAGTTGAGCACGCGCAGGCTGCGCATGCTGGCACCCTTGGCC CGCTAACCGTGCCCTTCCCTTGGCAGTTGAGC_CGCGCAGGCTGCGCATGCTGGCACCCTTGGCC GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55052697..55052807 26863196 MeRIP-seq:(Medium) rs779469742 Functional Loss DEL dbSNP153 33..33 33 - - - Clinvar_Rec_624 101715 RMVar_ID_101715 Human_SNP_ID_14068790 m1A Human chr1 + 55056098 55056098 55056098 TGGGTACAGCCGCGTCCTCAACGCCGCCTGCCAGCGCCTGGCGAGGGCTGGGGTCGTGCTGGTCA TGGGTACAGCCGCGTCCTCAACGCCGCCTGCCGGCGCCTGGCGAGGGCTGGGGTCGTGCTGGTCA A G PCSK9 Ensembl:ENSG00000169174 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:55056051..55056200 26863196 MeRIP-seq:(Medium) rs759388119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18474127,Human_RBP_ID_22427288,Human_RBP_ID_22531961,Human_RBP_ID_22751038 Human_Splice_Rec_75159,Human_Splice_Rec_75181,Human_Splice_Rec_75201 101716 RMVar_ID_101716 Human_SNP_ID_14070555 m1A Human chr1 + 55061465 55061465 55061465 GCCACGAGGTCAGCCCAACCAGTGCGTGGGCCACAGGGAGGCCAGCATCCACGCTTCCTGCTGCC GCCACGAGGTCAGCCCAACCAGTGCGTGGGCCGCAGGGAGGCCAGCATCCACGCTTCCTGCTGCC A G PCSK9 Ensembl:ENSG00000169174 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55061414..55061504 26863196 MeRIP-seq:(Medium) rs774174877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5137547,Human_RBP_ID_11040385,Human_RBP_ID_18468584,Human_RBP_ID_22427293,Human_RBP_ID_22751055 Human_Splice_Rec_75168,Human_Splice_Rec_75169,Human_Splice_Rec_75190,Human_Splice_Rec_75191,Human_Splice_Rec_75208,Human_Splice_Rec_75209,Human_Splice_Rec_75217 RMVar_hsa_circ_127585,RMVar_hsa_circ_133226 101717 RMVar_ID_101717 Human_SNP_ID_14072882 m1A Human chr1 + 55070257 55070257 55070257 GTATGCCAAGTGGAGAACGTCAAGAACAAGAGAGCTGGATGTTCATGTTCAGAAATCCAAGGTGG GTATGCCAAGTGGAGAACGTCAAGAACAAGAGGGCTGGATGTTCATGTTCAGAAATCCAAGGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55070255..55070382 26863196 MeRIP-seq:(Medium) rs1036904151 Functional Loss SNV dbSNP153 33..33 33 - - - 101718 RMVar_ID_101718 Human_SNP_ID_14086724 m1A Human chr1 + 55127916 55127916 55127916 CTCTATGCCCTGACGCTACCTTCCTGCCTTACACTTGCCACTCAGCTCTGACAGCTGGATTATGT CTCTATGCCCTGACGCTACCTTCCTGCCTTACGCTTGCCACTCAGCTCTGACAGCTGGATTATGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55127913..55128032 26863196 MeRIP-seq:(Medium) rs1364111473 Functional Loss SNV dbSNP153 33..33 33 - - - 101719 RMVar_ID_101719 Human_SNP_ID_14098185 m1A Human chr1 - 55178115 55178115 55178115 ATCCCTTTTCGTCAGAAGAATGATGAGAATGGAAACTGCTCAGGGGAAGGAATTGAATTCCCTAC ATCCCTTTTCGTCAGAAGAATGATGAGAATGGGAACTGCTCAGGGGAAGGAATTGAATTCCCTAC T C USP24 Ensembl:ENSG00000162402 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55178065..55178181 26863196 MeRIP-seq:(Medium) rs1025285704 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1750899,Human_RBP_ID_4060729,Human_RBP_ID_9271438,Human_RBP_ID_11042084,Human_RBP_ID_23403854,Human_RBP_ID_24713515 Human_Splice_Rec_75220 Human_miRNA_ID_1972047,Human_miRNA_ID_1974224,Human_miRNA_ID_2612050 RMVar_hsa_circ_28631,RMVar_hsa_circ_133244,RMVar_hsa_circ_81700,RMVar_hsa_circ_8743,RMVar_hsa_circ_97226,RMVar_hsa_circ_133268,RMVar_hsa_circ_133275,RMVar_hsa_circ_314278,RMVar_hsa_circ_9353 101720 RMVar_ID_101720 Human_SNP_ID_14098186 m1A Human chr1 - 55178115 55178115 55178115 ATCCCTTTTCGTCAGAAGAATGATGAGAATGGAAACTGCTCAGGGGAAGGAATTGAATTCCCTAC ATCCCTTTTCGTCAGAAGAATGATGAGAATGGCAACTGCTCAGGGGAAGGAATTGAATTCCCTAC T G USP24 Ensembl:ENSG00000162402 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55178065..55178181 26863196 MeRIP-seq:(Medium) rs1025285704 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1750899,Human_RBP_ID_4060729,Human_RBP_ID_9271438,Human_RBP_ID_11042084,Human_RBP_ID_23403854,Human_RBP_ID_24713515 Human_Splice_Rec_75220 Human_miRNA_ID_1972047,Human_miRNA_ID_1974224,Human_miRNA_ID_2612050 RMVar_hsa_circ_28631,RMVar_hsa_circ_133244,RMVar_hsa_circ_81700,RMVar_hsa_circ_8743,RMVar_hsa_circ_97226,RMVar_hsa_circ_133268,RMVar_hsa_circ_133275,RMVar_hsa_circ_314278,RMVar_hsa_circ_9353 101721 RMVar_ID_101721 Human_SNP_ID_14098629 m1A Human chr1 - 55179723 55179723 55179723 CCTGGGGATGGGGATGGGAGAACCAAGTGTTAAGAATGGAATTGGAGAGAAATGTATGAGGTCCA CCTGGGGATGGGGATGGGAGAACCAAGTGTTAGGAATGGAATTGGAGAGAAATGTATGAGGTCCA T C USP24 Ensembl:ENSG00000162402 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:55179721..55179817;chr1:55179721..55179832 26863196 MeRIP-seq:(Medium) rs1184159832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22563420 RMVar_hsa_circ_133244,RMVar_hsa_circ_81700,RMVar_hsa_circ_97226,RMVar_hsa_circ_133268 101722 RMVar_ID_101722 Human_SNP_ID_14106799 m1A Human chr1 - 55214099 55214099 55214099 TATGAGAGCAGTGGGGATTGCACTGAGAGGGCAGAGGTGGGAGGCCTGGGCAGGGGTGGGAGCTG TATGAGAGCAGTGGGGATTGCACTGAGAGGGCCGAGGTGGGAGGCCTGGGCAGGGGTGGGAGCTG T G USP24 Ensembl:ENSG00000162402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:55214097..55214186 26863196 MeRIP-seq:(Medium) rs1273325203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133244,RMVar_hsa_circ_81700,RMVar_hsa_circ_97226,RMVar_hsa_circ_133268 101723 RMVar_ID_101723 Human_SNP_ID_14107039 m1A Human chr1 - 55214889 55214880 55214889 GGGCCCGGCGGGGGCCCGCGGGGCGACGGCGGAGGTGACGGCGGCGGCGGCGGCCCCTCCCGCGG GGGCCCGGCGGGGGCCCGCGGGGCGACGGCGG_________CGGCGGCGGCGGCCCCTCCCGCGG GCCGTCACCT G USP24 Ensembl:ENSG00000162402 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:55214776..55215375;chr1:55214813..55215358 26863196 MeRIP-seq:(Medium) rs1557721813 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_8753996,Human_RBP_ID_9270172,Human_RBP_ID_9318976 Human_Splice_Rec_75219 RMVar_hsa_circ_133244,RMVar_hsa_circ_81700,RMVar_hsa_circ_97226,RMVar_hsa_circ_133268 101724 RMVar_ID_101724 Human_SNP_ID_14107075 m1A Human chr1 + 55214971 55214971 55214971 CGCTGTCCATGGGCTCGTAGCCGCCGTAGTCGAGGCCCGGCCGCTCGTTGGTGAGCAGTGCCACG CGCTGTCCATGGGCTCGTAGCCGCCGTAGTCGGGGCCCGGCCGCTCGTTGGTGAGCAGTGCCACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:55214813..55215349 26863196 MeRIP-seq:(Medium) rs1489097896 Functional Loss SNV dbSNP153 33..33 33 - - - 101725 RMVar_ID_101725 Human_SNP_ID_14439000 m1A Human chr1 - 56569709 56569709 56569709 GGCTGGAGAGATAGGTTAGAGCTAGATTATGAAAGGGGACTGGGTATGGCAGGCAGCTAAGGAAT GGCTGGAGAGATAGGTTAGAGCTAGATTATGAGAGGGGACTGGGTATGGCAGGCAGCTAAGGAAT T C PLPP3 Ensembl:ENSG00000162407 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:56569702..56569831 26863196 MeRIP-seq:(Medium) rs923533771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5843682 101726 RMVar_ID_101726 Human_SNP_ID_14456866 m1A Human chr1 + 56645385 56645385 56645385 CGGCAGGCGGTGGAGCGAGGCCGCGCGCGCCGAAGATGGCTGAGAAGCAGAAGCACGACGGGCGG CGGCAGGCGGTGGAGCGAGGCCGCGCGCGCCGCAGATGGCTGAGAAGCAGAAGCACGACGGGCGG A C PRKAA2 Ensembl:ENSG00000162409 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:56645330..56674413 26863196 MeRIP-seq:(Medium) rs1207748743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745366,Human_RBP_ID_9358891 Human_Splice_Rec_75701 101727 RMVar_ID_101727 Human_SNP_ID_14466120 m1A Human chr1 - 56684834 56684834 56684834 ACCTTGTTTAGACTCCTCATTTCCTTCTGGTTACCACTCCTATGTCTCTCCTCTCCTGCCTATAG ACCTTGTTTAGACTCCTCATTTCCTTCTGGTTGCCACTCCTATGTCTCTCCTCTCCTGCCTATAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:56684758..56684945 26863196 MeRIP-seq:(Medium) rs1249243431 Functional Loss SNV dbSNP153 33..33 33 - - - 101728 RMVar_ID_101728 Human_SNP_ID_14912566 m1A Human chr1 + 58543504 58543504 58543504 CCTTTCCTGGGCTCTGTGGTCTTATGGTGTTGATCACTACCCACCTAATCTCCCTGCCTTATTTC CCTTTCCTGGGCTCTGTGGTCTTATGGTGTTGCTCACTACCCACCTAATCTCCCTGCCTTATTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:58543453..58543593 26863196 MeRIP-seq:(Medium) rs60739996 Functional Loss SNV dbSNP153 33..33 33 - - - 101729 RMVar_ID_101729 Human_SNP_ID_14912567 m1A Human chr1 + 58543504 58543504 58543504 CCTTTCCTGGGCTCTGTGGTCTTATGGTGTTGATCACTACCCACCTAATCTCCCTGCCTTATTTC CCTTTCCTGGGCTCTGTGGTCTTATGGTGTTGGTCACTACCCACCTAATCTCCCTGCCTTATTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:58543453..58543593 26863196 MeRIP-seq:(Medium) rs60739996 Functional Loss SNV dbSNP153 33..33 33 - - - 101730 RMVar_ID_101730 Human_SNP_ID_14913356 m1A Human chr1 + 58546566 58546566 58546566 CACCCACGCCTCCTCCCGTACCCCCATCCCCAAGGATCCCCACTCCTTGCCCGGGCGCCCCCGCA CACCCACGCCTCCTCCCGTACCCCCATCCCCAGGGATCCCCACTCCTTGCCCGGGCGCCCCCGCA A G AL035411.3 Ensembl:ENSG00000286918 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58546563..58546781 26863196 MeRIP-seq:(Medium) rs899113366 Functional Loss SNV dbSNP153 33..33 33 - - - 101731 RMVar_ID_101731 Human_SNP_ID_14913370 m1A Human chr1 + 58546598 58546598 58546598 AGGATCCCCACTCCTTGCCCGGGCGCCCCCGCAGGCGCTCTGCGCTCCGCCCCCTCCCCACTGCC AGGATCCCCACTCCTTGCCCGGGCGCCCCCGCGGGCGCTCTGCGCTCCGCCCCCTCCCCACTGCC A G AL035411.3 Ensembl:ENSG00000286918 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:58546572..58546695 26863196 MeRIP-seq:(Medium) rs1006861374 Functional Loss SNV dbSNP153 33..33 33 - - - 101732 RMVar_ID_101732 Human_SNP_ID_14913387 m1A Human chr1 - 58546692 58546692 58546692 CACCGCTTTCGCTTCTGCTTGAGTCAGTCCTCACGGTGACGCTTTTCCCCAGCTTTTCCGAGTAG CACCGCTTTCGCTTCTGCTTGAGTCAGTCCTCCCGGTGACGCTTTTCCCCAGCTTTTCCGAGTAG T G DAB1,OMA1 Ensembl:ENSG00000173406,Ensembl:ENSG00000162600 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:58546539..58546774 26863196 MeRIP-seq:(Medium) rs1043436134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_76281,Human_Splice_Rec_76289,Human_Splice_Rec_76295,Human_Splice_Rec_76307,Human_Splice_Rec_76313 RMVar_hsa_circ_91862,RMVar_hsa_circ_133313 101733 RMVar_ID_101733 Human_SNP_ID_14920810 m1A Human chr1 + 58577107 58577107 58577107 TGTGGCCGGTCACCGCCGCCAGCACCAGCAGCAGCAGCGGCAGCCGCAGCGGTGGCGGCGCGAGG TGTGGCCGGTCACCGCCGCCAGCACCAGCAGCGGCAGCGGCAGCCGCAGCGGTGGCGGCGCGAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:58577056..58577319 26863196 MeRIP-seq:(Medium) rs1223775699 Functional Loss SNV dbSNP153 33..33 33 - - - 101734 RMVar_ID_101734 Human_SNP_ID_14920858 m1A Human chr1 - 58577210 58577210 58577210 AGACCATCCCAGACGCCGGAGCCCGAGCCCCGACGAGTCCCCGCGCCTCATCCGCCCGCGTCCGG AGACCATCCCAGACGCCGGAGCCCGAGCCCCGCCGAGTCCCCGCGCCTCATCCGCCCGCGTCCGG T G TACSTD2 Ensembl:ENSG00000184292 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58576963..58577337 26863196 MeRIP-seq:(Medium) rs232835 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_625 101735 RMVar_ID_101735 Human_SNP_ID_14929632 m1A Human chr1 - 58615805 58615805 58615805 AGGAGATAATAGGGGGAGGTACGAAAGGGGCCATAGTTGTTATGCATAGAGTGGAGAGGGGAGGT AGGAGATAATAGGGGGAGGTACGAAAGGGGCCGTAGTTGTTATGCATAGAGTGGAGAGGGGAGGT T C lnc-MYSM1-1 RNACentral:URS00008B5B4D lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:58615679..58615811 26863196 MeRIP-seq:(Medium) rs1040534503 Functional Loss SNV dbSNP153 33..33 33 - - - 101736 RMVar_ID_101736 Human_SNP_ID_14950378 m1A Human chr1 - 58700025 58700025 58700025 CCATCATGGCGGCTGAAGAGGCGGATGTGGATATCGAAGGGGACGTGGTAGCGGCGGCGGGGGCA CCATCATGGCGGCTGAAGAGGCGGATGTGGATGTCGAAGGGGACGTGGTAGCGGCGGCGGGGGCA T C MYSM1 Ensembl:ENSG00000162601 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:58692896..58700065 26863196 MeRIP-seq:(Medium) rs529415002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224430,Human_RBP_ID_745417,Human_RBP_ID_4061088,Human_RBP_ID_9356398,Human_RBP_ID_17646451,Human_RBP_ID_18414972,Human_RBP_ID_22871802,Human_RBP_ID_23404659,Human_RBP_ID_26311348,Human_RBP_ID_27798128 Human_Splice_Rec_76317,Human_Splice_Rec_76387,Human_Splice_Rec_76437,Human_Splice_Rec_76475,Human_Splice_Rec_76513,Human_Splice_Rec_76617,Human_Splice_Rec_76625 101737 RMVar_ID_101737 Human_SNP_ID_14950382 m1A Human chr1 - 58700033 58700033 58700033 GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGATGTGGATATCGAAGGGGACGTGGTAGCGGCGG GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGTTGTGGATATCGAAGGGGACGTGGTAGCGGCGG T A MYSM1 Ensembl:ENSG00000162601 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:58699921..58700065;chr1:58699921..58700045 26863196 MeRIP-seq:(Medium) rs1033445075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745417,Human_RBP_ID_9356398,Human_RBP_ID_11047527,Human_RBP_ID_18414972,Human_RBP_ID_22871802,Human_RBP_ID_26311348,Human_RBP_ID_27798128 Human_Splice_Rec_76317,Human_Splice_Rec_76387,Human_Splice_Rec_76437,Human_Splice_Rec_76475,Human_Splice_Rec_76513,Human_Splice_Rec_76617,Human_Splice_Rec_76625 101738 RMVar_ID_101738 Human_SNP_ID_14950383 m1A Human chr1 - 58700033 58700033 58700033 GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGATGTGGATATCGAAGGGGACGTGGTAGCGGCGG GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGGTGTGGATATCGAAGGGGACGTGGTAGCGGCGG T C MYSM1 Ensembl:ENSG00000162601 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:58699921..58700065;chr1:58699921..58700045 26863196 MeRIP-seq:(Medium) rs1033445075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745417,Human_RBP_ID_9356398,Human_RBP_ID_11047527,Human_RBP_ID_18414972,Human_RBP_ID_22871802,Human_RBP_ID_26311348,Human_RBP_ID_27798128 Human_Splice_Rec_76317,Human_Splice_Rec_76387,Human_Splice_Rec_76437,Human_Splice_Rec_76475,Human_Splice_Rec_76513,Human_Splice_Rec_76617,Human_Splice_Rec_76625 101739 RMVar_ID_101739 Human_SNP_ID_14950384 m1A Human chr1 - 58700033 58700033 58700033 GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGATGTGGATATCGAAGGGGACGTGGTAGCGGCGG GTCAGGTCCCATCATGGCGGCTGAAGAGGCGGCTGTGGATATCGAAGGGGACGTGGTAGCGGCGG T G MYSM1 Ensembl:ENSG00000162601 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:58699921..58700065;chr1:58699921..58700045 26863196 MeRIP-seq:(Medium) rs1033445075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745417,Human_RBP_ID_9356398,Human_RBP_ID_11047527,Human_RBP_ID_18414972,Human_RBP_ID_22871802,Human_RBP_ID_26311348,Human_RBP_ID_27798128 Human_Splice_Rec_76317,Human_Splice_Rec_76387,Human_Splice_Rec_76437,Human_Splice_Rec_76475,Human_Splice_Rec_76513,Human_Splice_Rec_76617,Human_Splice_Rec_76625 101740 RMVar_ID_101740 Human_SNP_ID_14955770 m1A Human chr1 - 58721204 58721200 58721204 TGCTCTCCCCACTTTCACAATAGTCTCCCCGAAACACACACACACACACACACACACACACACAC TGCTCTCCCCACTTTCACAATAGTCTCCCCGA____CACACACACACACACACACACACACACAC GTGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58721159..58721270 26863196 MeRIP-seq:(Medium) rs201604994 Functional Loss DEL dbSNP153 33..36 33 - - - 101741 RMVar_ID_101741 Human_SNP_ID_14955775 m1A Human chr1 - 58721204 58721204 58721204 TGCTCTCCCCACTTTCACAATAGTCTCCCCGAAACACACACACACACACACACACACACACACAC TGCTCTCCCCACTTTCACAATAGTCTCCCCGACACACACACACACACACACACACACACACACAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58721159..58721270 26863196 MeRIP-seq:(Medium) rs868556110 Functional Loss SNV dbSNP153 33..33 33 - - - 101742 RMVar_ID_101742 Human_SNP_ID_14955833 m1A Human chr1 + 58721423 58721423 58721423 TAGGTTTTCAGCTTGAGCAGTGCGAGGGATGCAGGTGCCGTTTGCTGAGATATGGAAGATTGGAG TAGGTTTTCAGCTTGAGCAGTGCGAGGGATGCGGGTGCCGTTTGCTGAGATATGGAAGATTGGAG A G AL136985.3 Ensembl:ENSG00000283445 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58721372..58721522 26863196 MeRIP-seq:(Medium) rs1198086737 Functional Loss SNV dbSNP153 33..33 33 - - - 101743 RMVar_ID_101743 Human_SNP_ID_14966203 m1A Human chr1 - 58762450 58762450 58762450 CCTCCAGCTTCATCCTGCATCACCTTCCTTTCATCTCTCTTCTCTCCAGCTCTTCTGGAAAGGAG CCTCCAGCTTCATCCTGCATCACCTTCCTTTCGTCTCTCTTCTCTCCAGCTCTTCTGGAAAGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58762290..58762455 26863196 MeRIP-seq:(Medium) rs1250427173 Functional Loss SNV dbSNP153 33..33 33 - - - 101744 RMVar_ID_101744 Human_SNP_ID_14970771 m1A Human chr1 + 58781820 58781820 58781820 AACGAAAAGTCCAACGTTCCGTTCGCGCGGGGACAGCCCGTCCGCAAAGCGGGGCAGCCCGCAGG AACGAAAAGTCCAACGTTCCGTTCGCGCGGGGGCAGCCCGTCCGCAAAGCGGGGCAGCCCGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:58781751..58781984 32194978 MeRIP-seq:(Medium) rs56090866 Functional Loss SNV dbSNP153 33..33 33 - - - 101745 RMVar_ID_101745 Human_SNP_ID_14970821 m1A Human chr1 - 58781958 58781958 58781958 AGAGAAAAAAGAAGTGTCCGAGAACTAAAGCCAAGGGTATCCAAGTTGGACTGGGTTGCGTCCTG AGAGAAAAAAGAAGTGTCCGAGAACTAAAGCCGAGGGTATCCAAGTTGGACTGGGTTGCGTCCTG T C JUN Ensembl:ENSG00000177606 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:58781912..58782048 26863196 MeRIP-seq:(Medium) rs959370227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25712,Human_RBP_ID_359155,Human_RBP_ID_1155357,Human_RBP_ID_1433060,Human_RBP_ID_1751146,Human_RBP_ID_3318056,Human_RBP_ID_4061154,Human_RBP_ID_5845410,Human_RBP_ID_8750847,Human_RBP_ID_11047570,Human_RBP_ID_18232234,Human_RBP_ID_23404684,Human_RBP_ID_26381870,Human_RBP_ID_26589257,Human_RBP_ID_26867434,Human_RBP_ID_27185278,Human_RBP_ID_27400252,Human_RBP_ID_27555637 Human_miRNA_ID_593376 101746 RMVar_ID_101746 Human_SNP_ID_14971072 m1A Human chr1 - 58782574 58782574 58782574 CAGCGGCGGCTTCAGCGCCAGCCTGCACAGCGAGCCGCCGGTCTACGCAAACCTCAGCAACTTCA CAGCGGCGGCTTCAGCGCCAGCCTGCACAGCGCGCCGCCGGTCTACGCAAACCTCAGCAACTTCA T G JUN Ensembl:ENSG00000177606 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:58782301..58782975 26863410 MeRIP-seq:(Medium) rs79353574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_979225,Human_RBP_ID_5845422,Human_RBP_ID_8750860 101747 RMVar_ID_101747 Human_SNP_ID_14971203 m1A Human chr1 - 58782901 58782901 58782901 GGGGAGCCTGAAGCCGCACCTCCGCGCCAAGAACTCGGACCTCCTCACCTCGCCCGACGTGGGGC GGGGAGCCTGAAGCCGCACCTCCGCGCCAAGATCTCGGACCTCCTCACCTCGCCCGACGTGGGGC T A JUN Ensembl:ENSG00000177606 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:58782801..58782917 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_746724,Human_RBP_ID_979228,Human_RBP_ID_1433077,Human_RBP_ID_4061193,Human_RBP_ID_5845430,Human_RBP_ID_8750864,Human_RBP_ID_9268954,Human_RBP_ID_9358910,Human_RBP_ID_11047579,Human_RBP_ID_22023433,Human_RBP_ID_26867452,Human_RBP_ID_27400263 101748 RMVar_ID_101748 Human_SNP_ID_15219400 m1A Human chr1 - 59815000 59815000 59815000 CTAGCCCCCAGGAAAGCTCGGTACCAGGCCCGACCCGCGCAGCTCACGCGCGAACCCTCGCGCTG CTAGCCCCCAGGAAAGCTCGGTACCAGGCCCGGCCCGCGCAGCTCACGCGCGAACCCTCGCGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:59814876..59815130;chr1:59814882..59815136 26863196 MeRIP-seq:(Medium) rs1017658273 Functional Loss SNV dbSNP153 33..33 33 - - - 101749 RMVar_ID_101749 Human_SNP_ID_15219416 m1A Human chr1 + 59815043 59815043 59815043 ACCGAGCTTTCCTGGGGGCTAGCAGGTCGTGGACGCCGGCTCCTGGAGGAGAGCCGGTAGGAGGG ACCGAGCTTTCCTGGGGGCTAGCAGGTCGTGGGCGCCGGCTCCTGGAGGAGAGCCGGTAGGAGGG A G HOOK1 Ensembl:ENSG00000134709 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:59814861..59815127 26863196 MeRIP-seq:(Medium) rs1559038823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4072854,Human_RBP_ID_9358915,Human_RBP_ID_11047800,Human_RBP_ID_18414973 Human_Splice_Rec_77426 101750 RMVar_ID_101750 Human_SNP_ID_15219436 m1A Human chr1 - 59815080 59815080 59815080 GCGCCGCCGTCGACGACGCCGCGGACACCTTCACACTCCCTCCTACCGGCTCTCCTCCAGGAGCC GCGCCGCCGTCGACGACGCCGCGGACACCTTCCCACTCCCTCCTACCGGCTCTCCTCCAGGAGCC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:59814964..59815109;chr1:59814907..59815134 26863196 MeRIP-seq:(Medium) rs1347913924 Functional Loss SNV dbSNP153 33..33 33 - - - 101751 RMVar_ID_101751 Human_SNP_ID_386479731 m1A Human chr9 - 11200 11200 11200 CGCGCCGCCGTGACGTGAGTTTCTGCGCGTGCACGGCGCCCCCCCCCCCCCCCCCCCCCCCGCCC CGCGCCGCCGTGACGTGAGTTTCTGCGCGTGCCCGGCGCCCCCCCCCCCCCCCCCCCCCCCGCCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:11071..11290 26863196 MeRIP-seq:(Medium) rs1330537123 Functional Loss SNV dbSNP153 33..33 33 - - - 101752 RMVar_ID_101752 Human_SNP_ID_386479732 m1A Human chr9 + 11203 11203 11203 CGGGGGGGGGGGGGGGGGGGGGGGCGCCGTGCACGCGCAGAAACTCACGTCACGGCGGCGCGGCG CGGGGGGGGGGGGGGGGGGGGGGGCGCCGTGCGCGCGCAGAAACTCACGTCACGGCGGCGCGGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr9:11072..11285;chr9:11088..11273 26863196 MeRIP-seq:(Medium) rs1208550643 Functional Loss SNV dbSNP153 33..33 33 - - - 101753 RMVar_ID_101753 Human_SNP_ID_386481531 m1A Human chr9 - 14710 14710 14710 CAGGACAAGCTGCTCAGACCTGCTTCCCTGGGAGGGGGTGACGGAACCAGCAGTGTGTGGAGACC CAGGACAAGCTGCTCAGACCTGCTTCCCTGGGTGGGGGTGACGGAACCAGCAGTGTGTGGAGACC T A WASHC1 Ensembl:ENSG00000181404 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1404595755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18172953 101754 RMVar_ID_101754 Human_SNP_ID_386481671 m1A Human chr9 + 14889 14889 14889 GCGGCAAAGGAGGGATGGAGTCTGACACGCGGACAAAGGCTCCTCCGGGCCCCTCACCAGCCCCA GCGGCAAAGGAGGGATGGAGTCTGACACGCGGGCAAAGGCTCCTCCGGGCCCCTCACCAGCCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:14816..14916 32194978 MeRIP-seq:(Medium) rs71509924 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 101755 RMVar_ID_101755 Human_SNP_ID_386528560 m1A Human chr9 - 173218 173218 173218 TGTACATGGTTTACTAGAAATGTTTATTGATTATATTTCCAGCTTTAATTTTCTTGAGTAATTTA TGTACATGGTTTACTAGAAATGTTTATTGATTGTATTTCCAGCTTTAATTTTCTTGAGTAATTTA T C CBWD1 Ensembl:ENSG00000172785 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1554633552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_155594,Human_miRNA_ID_898797,Human_miRNA_ID_905458,Human_miRNA_ID_912100,Human_miRNA_ID_918732,Human_miRNA_ID_1120949,Human_miRNA_ID_1128088,Human_miRNA_ID_1216151,Human_miRNA_ID_1282330 RMVar_hsa_circ_2994,RMVar_hsa_circ_73448,RMVar_hsa_circ_255221,RMVar_hsa_circ_333643 101756 RMVar_ID_101756 Human_SNP_ID_386628923 m1A Human chr9 - 470352 470352 470352 GGCCACGCACCCTCTCACTTTGCTAATTTCCAACCACTCGCTGCTGAGCAGGCTGGAGCACGCCC GGCCACGCACCCTCTCACTTTGCTAATTTCCAGCCACTCGCTGCTGAGCAGGCTGGAGCACGCCC T C AL161725.1 Ensembl:ENSG00000227155 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:470302..470467 26863196 MeRIP-seq:(Medium) rs1023055028 Functional Loss SNV dbSNP153 33..33 33 - - - 101757 RMVar_ID_101757 Human_SNP_ID_386628925 m1A Human chr9 + 470356 470356 470356 GTGCTCCAGCCTGCTCAGCAGCGAGTGGTTGGAAATTAGCAAAGTGAGAGGGTGCGTGGCCTGAG GTGCTCCAGCCTGCTCAGCAGCGAGTGGTTGGGAATTAGCAAAGTGAGAGGGTGCGTGGCCTGAG A G KANK1 Ensembl:ENSG00000107104 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:470305..470594 26863196 MeRIP-seq:(Medium) rs145566222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1027059 101758 RMVar_ID_101758 Human_SNP_ID_386639832 m1A Human chr9 + 505392 505392 505392 GGGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCAACCCGGCGCGGGCAGCGTGGGTTTCCGAGGTC GGGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCCACCCGGCGCGGGCAGCGTGGGTTTCCGAGGTC A C KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:505383..505540 26863196 MeRIP-seq:(Medium) rs918062726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 101759 RMVar_ID_101759 Human_SNP_ID_386639833 m1A Human chr9 + 505393 505393 505393 GGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCAACCCGGCGCGGGCAGCGTGGGTTTCCGAGGTCC GGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCAGCCCGGCGCGGGCAGCGTGGGTTTCCGAGGTCC A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:505392..505521 26863196 MeRIP-seq:(Medium) rs1007124385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 101760 RMVar_ID_101760 Human_SNP_ID_386639834 m1A Human chr9 + 505393 505393 505393 GGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCAACCCGGCGCGGGCAGCGTGGGTTTCCGAGGTCC GGCGTGGGCGCTGCGGCCTCTGGGGCGGCCCATCCCGGCGCGGGCAGCGTGGGTTTCCGAGGTCC A T KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:505392..505521 26863196 MeRIP-seq:(Medium) rs1007124385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 101761 RMVar_ID_101761 Human_SNP_ID_386654525 m1A Human chr9 - 544660 544660 544660 AACTACGACCTCCACCTCCCATTAATGTTCCCAGTATGAAGCGCCCATAACAGCCCGTACTTCCC AACTACGACCTCCACCTCCCATTAATGTTCCCGGTATGAAGCGCCCATAACAGCCCGTACTTCCC T C RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:544658..544781 26863196 MeRIP-seq:(Medium) rs1563745311 Functional Loss SNV dbSNP153 33..33 33 - - - 101762 RMVar_ID_101762 Human_SNP_ID_386654591 m1A Human chr9 - 544905 544905 544905 CCTCCAGCCAGCACTTCACCTACCAACTTAAAACTTGCCAGTGATTTCCCACAACTCTTGAGATA CCTCCAGCCAGCACTTCACCTACCAACTTAAACCTTGCCAGTGATTTCCCACAACTCTTGAGATA T G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:544899..545088 26863196 MeRIP-seq:(Medium) rs1275605901 Functional Loss SNV dbSNP153 33..33 33 - - - 101763 RMVar_ID_101763 Human_SNP_ID_386656721 m1A Human chr9 + 551056 551056 551056 GAGATGGGTCAGGGAGGAAAGCCAAGATGGAAAATGGATGGGAATGAATGAGGAACATGATGTGG GAGATGGGTCAGGGAGGAAAGCCAAGATGGAAGATGGATGGGAATGAATGAGGAACATGATGTGG A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:551051..551140 26863196 MeRIP-seq:(Medium) rs1357934826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24304610 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_255236 101764 RMVar_ID_101764 Human_SNP_ID_386659179 m1A Human chr9 + 558080 558080 558080 AGGAACCCAGGAGTGAAGATCGGATTAGTCAGATGCTGTGAGAGGAGGTGGAAAAAACCAGTGTA AGGAACCCAGGAGTGAAGATCGGATTAGTCAGCTGCTGTGAGAGGAGGTGGAAAAAACCAGTGTA A C KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:558079..558160 26863196 MeRIP-seq:(Medium) rs1208135254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929947,Human_RBP_ID_24304617 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_255236 101765 RMVar_ID_101765 Human_SNP_ID_386659180 m1A Human chr9 + 558080 558080 558080 AGGAACCCAGGAGTGAAGATCGGATTAGTCAGATGCTGTGAGAGGAGGTGGAAAAAACCAGTGTA AGGAACCCAGGAGTGAAGATCGGATTAGTCAGGTGCTGTGAGAGGAGGTGGAAAAAACCAGTGTA A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:558079..558160 26863196 MeRIP-seq:(Medium) rs1208135254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929947,Human_RBP_ID_24304617 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_255236 101766 RMVar_ID_101766 Human_SNP_ID_386673059 m1A Human chr9 + 596406 596406 596406 TGTACATCACTGTAGGTTAAGTTCGGGTAGAGAAAAGACTAAAGGCAACCAAGGCTGGCTGTCCT TGTACATCACTGTAGGTTAAGTTCGGGTAGAGGAAAGACTAAAGGCAACCAAGGCTGGCTGTCCT A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:596387..596471 26863410 MeRIP-seq:(Medium) rs921297055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3217866,Human_RBP_ID_16687152 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_255236 101767 RMVar_ID_101767 Human_SNP_ID_386710579 m1A Human chr9 - 699483 699483 699483 TTTTAACAGACATTAACCTGCACACTACTCCTACATCTTCCACTGTCTCCCATCACTACCCTTCT TTTTAACAGACATTAACCTGCACACTACTCCTGCATCTTCCACTGTCTCCCATCACTACCCTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:699465..699557 26863196 MeRIP-seq:(Medium) rs974728543 Functional Loss SNV dbSNP153 33..33 33 - - - 101768 RMVar_ID_101768 Human_SNP_ID_386714813 m1A Human chr9 + 711815 711815 711815 AAGAAGTGGCGGGGAATTATACATTGACTATGAGGAGGAAGAAATGGAGACCGTAGAACAGAGCA AAGAAGTGGCGGGGAATTATACATTGACTATGGGGAGGAAGAAATGGAGACCGTAGAACAGAGCA A G KANK1 Ensembl:ENSG00000107104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:711765..711852 26863196 MeRIP-seq:(Medium) rs1564041402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90580 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_71508,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_366385,RMVar_hsa_circ_356606,RMVar_hsa_circ_276901,RMVar_hsa_circ_362413,RMVar_hsa_circ_255237 101769 RMVar_ID_101769 Human_SNP_ID_386722591 m1A Human chr9 + 732495 732495 732495 CCTCTTGAAGAAGAGGAGGAGGAGGAGGATGAAGACACTCGGGGAATGGCAGAAGGGCACCATGC CCTCTTGAAGAAGAGGAGGAGGAGGAGGATGACGACACTCGGGGAATGGCAGAAGGGCACCATGC A C KANK1 Ensembl:ENSG00000107104 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:732444..732562 26863196 MeRIP-seq:(Medium) rs760526483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797205,Human_RBP_ID_847628,Human_RBP_ID_8239140,Human_RBP_ID_9406741,Human_RBP_ID_24549685 RMVar_hsa_circ_1292,RMVar_hsa_circ_105660,RMVar_hsa_circ_255234,RMVar_hsa_circ_71508,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_366385,RMVar_hsa_circ_94505,RMVar_hsa_circ_371358,RMVar_hsa_circ_327369,RMVar_hsa_circ_255238,RMVar_hsa_circ_348426,RMVar_hsa_circ_71118,RMVar_hsa_circ_255239 101770 RMVar_ID_101770 Human_SNP_ID_386722592 m1A Human chr9 + 732495 732495 732495 CCTCTTGAAGAAGAGGAGGAGGAGGAGGATGAAGACACTCGGGGAATGGCAGAAGGGCACCATGC CCTCTTGAAGAAGAGGAGGAGGAGGAGGATGAGGACACTCGGGGAATGGCAGAAGGGCACCATGC A G KANK1 Ensembl:ENSG00000107104 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:732444..732562 26863196 MeRIP-seq:(Medium) rs760526483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797205,Human_RBP_ID_847628,Human_RBP_ID_8239140,Human_RBP_ID_9406741,Human_RBP_ID_24549685 RMVar_hsa_circ_1292,RMVar_hsa_circ_105660,RMVar_hsa_circ_255234,RMVar_hsa_circ_71508,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041,RMVar_hsa_circ_366385,RMVar_hsa_circ_94505,RMVar_hsa_circ_371358,RMVar_hsa_circ_327369,RMVar_hsa_circ_255238,RMVar_hsa_circ_348426,RMVar_hsa_circ_71118,RMVar_hsa_circ_255239 101771 RMVar_ID_101771 Human_SNP_ID_387182992 m1A Human chr9 - 2015998 2015998 2015998 GTGGCAACAGCGTCCGTTGGCGCCCCGCCGCCAGCCTGGGCTCCCCGCCCTCCTTTCCCGTTCCC GTGGCAACAGCGTCCGTTGGCGCCCCGCCGCCGGCCTGGGCTCCCCGCCCTCCTTTCCCGTTCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2015990..2016084 26863196 MeRIP-seq:(Medium) rs1393893655 Functional Loss SNV dbSNP153 33..33 33 - - - 101772 RMVar_ID_101772 Human_SNP_ID_387183528 m1A Human chr9 + 2017402 2017402 2017402 CGCGAGTGTGTCTGCGCGTGAGTGTGAGTGTGAGTGTGTGTTGTGCGCGCAGGAGCCAGTGCGTC CGCGAGTGTGTCTGCGCGTGAGTGTGAGTGTGTGTGTGTGTTGTGCGCGCAGGAGCCAGTGCGTC A T SMARCA2 Ensembl:ENSG00000080503 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2017328..2017611 26863196 MeRIP-seq:(Medium) rs1384940932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5329425,Human_RBP_ID_9339415,Human_RBP_ID_22629048,Human_RBP_ID_24296200 RMVar_hsa_circ_92658,RMVar_hsa_circ_123408,RMVar_hsa_circ_255244,RMVar_hsa_circ_255245 101773 RMVar_ID_101773 Human_SNP_ID_387183593 m1A Human chr9 - 2017539 2017539 2017539 TCGCGCGCGCACACACACACACTCACAACCACACGCACACGCCACCCCCACCAGCCCTCGCCACC TCGCGCGCGCACACACACACACTCACAACCACCCGCACACGCCACCCCCACCAGCCCTCGCCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:2017349..2017748 26863196 MeRIP-seq:(Medium) rs1185785131 Functional Loss SNV dbSNP153 33..33 33 - - - 101774 RMVar_ID_101774 Human_SNP_ID_387189935 m1A Human chr9 + 2039561 2039561 2039561 GAGGAGGCCCAACTCCACCTCAGATGCCACCAAGCCAGCCGGGGGCCCTCATCCCAGGTGATCCG GAGGAGGCCCAACTCCACCTCAGATGCCACCACGCCAGCCGGGGGCCCTCATCCCAGGTGATCCG A C SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2039512..2039593 26863196 MeRIP-seq:(Medium) rs1458030160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26361580,Human_RBP_ID_26833866 Human_Splice_Rec_1027344,Human_Splice_Rec_1027408,Human_Splice_Rec_1027470,Human_Splice_Rec_1027476,Human_Splice_Rec_1027488,Human_Splice_Rec_1027494,Human_Splice_Rec_1027560,Human_Splice_Rec_1027572,Human_Splice_Rec_1027576,Human_Splice_Rec_1027640,Human_Splice_Rec_1027646,Human_Splice_Rec_1027710,Human_Splice_Rec_1027718,Human_Splice_Rec_1027784 Human_miRNA_ID_2295386 RMVar_hsa_circ_36257,RMVar_hsa_circ_123408,RMVar_hsa_circ_255244,RMVar_hsa_circ_62344,RMVar_hsa_circ_320003,RMVar_hsa_circ_353473,RMVar_hsa_circ_279293,RMVar_hsa_circ_292817,RMVar_hsa_circ_69602,RMVar_hsa_circ_356036,RMVar_hsa_circ_81985,RMVar_hsa_circ_59793,RMVar_hsa_circ_255247,RMVar_hsa_circ_255248,RMVar_hsa_circ_368024,RMVar_hsa_circ_291067,RMVar_hsa_circ_324134,RMVar_hsa_circ_70308,RMVar_hsa_circ_255249,RMVar_hsa_circ_255251,RMVar_hsa_circ_33087,RMVar_hsa_circ_255252,RMVar_hsa_circ_255250,RMVar_hsa_circ_255253,RMVar_hsa_circ_255254 101775 RMVar_ID_101775 Human_SNP_ID_387189936 m1A Human chr9 + 2039561 2039561 2039561 GAGGAGGCCCAACTCCACCTCAGATGCCACCAAGCCAGCCGGGGGCCCTCATCCCAGGTGATCCG GAGGAGGCCCAACTCCACCTCAGATGCCACCAGGCCAGCCGGGGGCCCTCATCCCAGGTGATCCG A G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2039512..2039593 26863196 MeRIP-seq:(Medium) rs1458030160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26361580,Human_RBP_ID_26833866 Human_Splice_Rec_1027344,Human_Splice_Rec_1027408,Human_Splice_Rec_1027470,Human_Splice_Rec_1027476,Human_Splice_Rec_1027488,Human_Splice_Rec_1027494,Human_Splice_Rec_1027560,Human_Splice_Rec_1027572,Human_Splice_Rec_1027576,Human_Splice_Rec_1027640,Human_Splice_Rec_1027646,Human_Splice_Rec_1027710,Human_Splice_Rec_1027718,Human_Splice_Rec_1027784 Human_miRNA_ID_2295386 RMVar_hsa_circ_36257,RMVar_hsa_circ_123408,RMVar_hsa_circ_255244,RMVar_hsa_circ_62344,RMVar_hsa_circ_320003,RMVar_hsa_circ_353473,RMVar_hsa_circ_279293,RMVar_hsa_circ_292817,RMVar_hsa_circ_69602,RMVar_hsa_circ_356036,RMVar_hsa_circ_81985,RMVar_hsa_circ_59793,RMVar_hsa_circ_255247,RMVar_hsa_circ_255248,RMVar_hsa_circ_368024,RMVar_hsa_circ_291067,RMVar_hsa_circ_324134,RMVar_hsa_circ_70308,RMVar_hsa_circ_255249,RMVar_hsa_circ_255251,RMVar_hsa_circ_33087,RMVar_hsa_circ_255252,RMVar_hsa_circ_255250,RMVar_hsa_circ_255253,RMVar_hsa_circ_255254 101776 RMVar_ID_101776 Human_SNP_ID_387196462 m1A Human chr9 - 2060896 2060896 2060896 CAAACCAGATTGGTCAGATTGGCTACATACTCATCGGTCTGCTGCAAAAGGTAAGCTAAACGCCT CAAACCAGATTGGTCAGATTGGCTACATACTCGTCGGTCTGCTGCAAAAGGTAAGCTAAACGCCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:2060856..2060991 26863196 MeRIP-seq:(Medium) rs751020630 Functional Loss SNV dbSNP153 33..33 33 - - - 101777 RMVar_ID_101777 Human_SNP_ID_387196495 m1A Human chr9 + 2060982 2060982 2060982 AGCCAAAGAGAAGAAGAAGAGGAGGAGGAGGAAGAAGGTGCGTATCCTAGTGGTGGTGGCTGAGT AGCCAAAGAGAAGAAGAAGAGGAGGAGGAGGAGGAAGGTGCGTATCCTAGTGGTGGTGGCTGAGT A G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:2060877..2061032;chr9:2060874..2061052 26863196 MeRIP-seq:(Medium) rs1208316807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26361582 Human_Splice_Rec_1027355,Human_Splice_Rec_1027419,Human_Splice_Rec_1027505,Human_Splice_Rec_1027587,Human_Splice_Rec_1027657,Human_Splice_Rec_1027729 RMVar_hsa_circ_12090,RMVar_hsa_circ_36257,RMVar_hsa_circ_123408,RMVar_hsa_circ_255244,RMVar_hsa_circ_62344,RMVar_hsa_circ_320003,RMVar_hsa_circ_353473,RMVar_hsa_circ_292817,RMVar_hsa_circ_81985,RMVar_hsa_circ_255248,RMVar_hsa_circ_368024,RMVar_hsa_circ_324134,RMVar_hsa_circ_70308,RMVar_hsa_circ_255249,RMVar_hsa_circ_255251,RMVar_hsa_circ_33087,RMVar_hsa_circ_255250,RMVar_hsa_circ_285366,RMVar_hsa_circ_322223,RMVar_hsa_circ_346338,RMVar_hsa_circ_322068,RMVar_hsa_circ_42621,RMVar_hsa_circ_47713,RMVar_hsa_circ_40050,RMVar_hsa_circ_28206,RMVar_hsa_circ_55898,RMVar_hsa_circ_255255,RMVar_hsa_circ_255256,RMVar_hsa_circ_73109,RMVar_hsa_circ_34846,RMVar_hsa_circ_22784 101778 RMVar_ID_101778 Human_SNP_ID_387199543 m1A Human chr9 - 2070465 2070465 2070465 CAGTGGAAAGGATGACGATCCCTTACCTCTCCATCCGGTCCCAGGGCAGACTCCCCACCCTCTGC CAGTGGAAAGGATGACGATCCCTTACCTCTCCGTCCGGTCCCAGGGCAGACTCCCCACCCTCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2070401..2070475 26863196 MeRIP-seq:(Medium) rs1298701722 Functional Loss SNV dbSNP153 33..33 33 - - - 101779 RMVar_ID_101779 Human_SNP_ID_387215036 m1A Human chr9 + 2123826 2123826 2123826 CTGCCCTCCTGGATCATTAAGGATGACGCTGAAGTAGAAAGGCTCACCTGTGAAGAAGAGGAGGA CTGCCCTCCTGGATCATTAAGGATGACGCTGACGTAGAAAGGCTCACCTGTGAAGAAGAGGAGGA A C SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2123776..2123962 26863196 MeRIP-seq:(Medium) rs757958573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2890224 RMVar_hsa_circ_62344,RMVar_hsa_circ_320003,RMVar_hsa_circ_292817,RMVar_hsa_circ_324134,RMVar_hsa_circ_33087,RMVar_hsa_circ_322223,RMVar_hsa_circ_322068,RMVar_hsa_circ_42621,RMVar_hsa_circ_8082,RMVar_hsa_circ_55898,RMVar_hsa_circ_255256,RMVar_hsa_circ_73109,RMVar_hsa_circ_266187,RMVar_hsa_circ_19402,RMVar_hsa_circ_67416,RMVar_hsa_circ_350720,RMVar_hsa_circ_255262,RMVar_hsa_circ_335629,RMVar_hsa_circ_302958,RMVar_hsa_circ_255263,RMVar_hsa_circ_376486,RMVar_hsa_circ_353452,RMVar_hsa_circ_255268,RMVar_hsa_circ_304554,RMVar_hsa_circ_255267,RMVar_hsa_circ_57777,RMVar_hsa_circ_255269,RMVar_hsa_circ_322290,RMVar_hsa_circ_378788,RMVar_hsa_circ_255271,RMVar_hsa_circ_305469,RMVar_hsa_circ_331713,RMVar_hsa_circ_255270,RMVar_hsa_circ_255272 101780 RMVar_ID_101780 Human_SNP_ID_387215037 m1A Human chr9 + 2123826 2123826 2123826 CTGCCCTCCTGGATCATTAAGGATGACGCTGAAGTAGAAAGGCTCACCTGTGAAGAAGAGGAGGA CTGCCCTCCTGGATCATTAAGGATGACGCTGAGGTAGAAAGGCTCACCTGTGAAGAAGAGGAGGA A G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2123776..2123962 26863196 MeRIP-seq:(Medium) rs757958573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2890224 RMVar_hsa_circ_62344,RMVar_hsa_circ_320003,RMVar_hsa_circ_292817,RMVar_hsa_circ_324134,RMVar_hsa_circ_33087,RMVar_hsa_circ_322223,RMVar_hsa_circ_322068,RMVar_hsa_circ_42621,RMVar_hsa_circ_8082,RMVar_hsa_circ_55898,RMVar_hsa_circ_255256,RMVar_hsa_circ_73109,RMVar_hsa_circ_266187,RMVar_hsa_circ_19402,RMVar_hsa_circ_67416,RMVar_hsa_circ_350720,RMVar_hsa_circ_255262,RMVar_hsa_circ_335629,RMVar_hsa_circ_302958,RMVar_hsa_circ_255263,RMVar_hsa_circ_376486,RMVar_hsa_circ_353452,RMVar_hsa_circ_255268,RMVar_hsa_circ_304554,RMVar_hsa_circ_255267,RMVar_hsa_circ_57777,RMVar_hsa_circ_255269,RMVar_hsa_circ_322290,RMVar_hsa_circ_378788,RMVar_hsa_circ_255271,RMVar_hsa_circ_305469,RMVar_hsa_circ_331713,RMVar_hsa_circ_255270,RMVar_hsa_circ_255272 101781 RMVar_ID_101781 Human_SNP_ID_387227371 m1A Human chr9 + 2161742 2161742 2161742 GAAATGGAAGAGGAAGTACGGCTTAAGAAGCGAAAAAGACGAAGAAATGTGGATAAAGATCCTGC GAAATGGAAGAGGAAGTACGGCTTAAGAAGCGGAAAAGACGAAGAAATGTGGATAAAGATCCTGC A G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2161647..2161832 26863196 MeRIP-seq:(Medium) rs1298163376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90196,Human_RBP_ID_22119777,Human_RBP_ID_26361590,Human_RBP_ID_27832973 Human_Splice_Rec_1027392,Human_Splice_Rec_1027456,Human_Splice_Rec_1027542,Human_Splice_Rec_1027624,Human_Splice_Rec_1027694,Human_Splice_Rec_1027766,Human_Splice_Rec_1027832,Human_Splice_Rec_1027892,Human_Splice_Rec_1027914,Human_Splice_Rec_1027952,Human_Splice_Rec_1027970,Human_Splice_Rec_1027978,Human_Splice_Rec_1027988,Human_Splice_Rec_1027998,Human_Splice_Rec_1028012,Human_Splice_Rec_1028020,Human_Splice_Rec_1028036,Human_Splice_Rec_1028048,Human_Splice_Rec_1028064,Human_Splice_Rec_1028080,Human_Splice_Rec_1028094,Human_Splice_Rec_1028106,Human_Splice_Rec_1028120,Human_Splice_Rec_1028138,Human_Splice_Rec_1028152,Human_Splice_Rec_1028168,Human_Splice_Rec_1028178,Human_Splice_Rec_1028188,Human_Splice_Rec_1028198,Human_Splice_Rec_1028210,Human_Splice_Rec_1028214,Human_Splice_Rec_1028228,Human_Splice_Rec_1028230,Human_Splice_Rec_1028238,Human_Splice_Rec_1028248,Human_Splice_Rec_1028260,Human_Splice_Rec_1028262,Human_Splice_Rec_1028274 RMVar_hsa_circ_62344,RMVar_hsa_circ_292817,RMVar_hsa_circ_324134,RMVar_hsa_circ_322068,RMVar_hsa_circ_42621,RMVar_hsa_circ_55898,RMVar_hsa_circ_19402,RMVar_hsa_circ_67416,RMVar_hsa_circ_350720,RMVar_hsa_circ_255262,RMVar_hsa_circ_335629,RMVar_hsa_circ_353452,RMVar_hsa_circ_255268,RMVar_hsa_circ_322290,RMVar_hsa_circ_255271,RMVar_hsa_circ_331713,RMVar_hsa_circ_255272,RMVar_hsa_circ_255274,RMVar_hsa_circ_255275,RMVar_hsa_circ_285797 101782 RMVar_ID_101782 Human_SNP_ID_387236506 m1A Human chr9 + 2186196 2186191 2186197 AGAGAGTGAGGATGAAAGCAATGAAGAGGAGGAAGAGGAAGATGAAGAAGAGTCAGAGTCCGAGG AGAGAGTGAGGATGAAAGCAATGAAGAG______GAGGAAGATGAAGAAGAGTCAGAGTCCGAGG GGAGGAA G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:2186146..2186284 26863196 MeRIP-seq:(Medium) rs1373436130 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_846422,Human_RBP_ID_7916318,Human_RBP_ID_24549687,Human_RBP_ID_26360565 Human_Splice_Rec_1027399,Human_Splice_Rec_1027463,Human_Splice_Rec_1027551,Human_Splice_Rec_1027631,Human_Splice_Rec_1027701,Human_Splice_Rec_1027775,Human_Splice_Rec_1027839,Human_Splice_Rec_1027921,Human_Splice_Rec_1027961,Human_Splice_Rec_1027985,Human_Splice_Rec_1028005,Human_Splice_Rec_1028029,Human_Splice_Rec_1028043,Human_Splice_Rec_1028055,Human_Splice_Rec_1028071,Human_Splice_Rec_1028087,Human_Splice_Rec_1028101,Human_Splice_Rec_1028113,Human_Splice_Rec_1028127,Human_Splice_Rec_1028145,Human_Splice_Rec_1028161,Human_Splice_Rec_1028175,Human_Splice_Rec_1028185,Human_Splice_Rec_1028207,Human_Splice_Rec_1028223,Human_Splice_Rec_1028245,Human_Splice_Rec_1028255,Human_Splice_Rec_1028269,Human_Splice_Rec_1028287 RMVar_hsa_circ_62344,RMVar_hsa_circ_42621,RMVar_hsa_circ_255274,RMVar_hsa_circ_74542,RMVar_hsa_circ_310532,RMVar_hsa_circ_255276,RMVar_hsa_circ_255277 101783 RMVar_ID_101783 Human_SNP_ID_387238620 m1A Human chr9 + 2191354 2191354 2191354 AAAGGGAAAGGCAAGAAAAGGCCAAATCGAGGAAAAGCCAAACCTGTAGTGAGCGATTTTGACAG AAAGGGAAAGGCAAGAAAAGGCCAAATCGAGGGAAAGCCAAACCTGTAGTGAGCGATTTTGACAG A G SMARCA2 Ensembl:ENSG00000080503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2191265..2191384 26863196 MeRIP-seq:(Medium) rs916389765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5228388,Human_RBP_ID_16643247 Human_Splice_Rec_1027400,Human_Splice_Rec_1027401,Human_Splice_Rec_1027464,Human_Splice_Rec_1027465,Human_Splice_Rec_1027552,Human_Splice_Rec_1027553,Human_Splice_Rec_1027632,Human_Splice_Rec_1027633,Human_Splice_Rec_1027702,Human_Splice_Rec_1027703,Human_Splice_Rec_1027776,Human_Splice_Rec_1027777,Human_Splice_Rec_1027840,Human_Splice_Rec_1027841,Human_Splice_Rec_1027922,Human_Splice_Rec_1027923,Human_Splice_Rec_1027962,Human_Splice_Rec_1027963,Human_Splice_Rec_1027986,Human_Splice_Rec_1028006,Human_Splice_Rec_1028007,Human_Splice_Rec_1028030,Human_Splice_Rec_1028031,Human_Splice_Rec_1028044,Human_Splice_Rec_1028056,Human_Splice_Rec_1028057,Human_Splice_Rec_1028072,Human_Splice_Rec_1028073,Human_Splice_Rec_1028088,Human_Splice_Rec_1028089,Human_Splice_Rec_1028102,Human_Splice_Rec_1028103,Human_Splice_Rec_1028114,Human_Splice_Rec_1028115,Human_Splice_Rec_1028128,Human_Splice_Rec_1028129,Human_Splice_Rec_1028146,Human_Splice_Rec_1028147,Human_Splice_Rec_1028162,Human_Splice_Rec_1028163,Human_Splice_Rec_1028176,Human_Splice_Rec_1028186,Human_Splice_Rec_1028208,Human_Splice_Rec_1028224,Human_Splice_Rec_1028246,Human_Splice_Rec_1028256,Human_Splice_Rec_1028270,Human_Splice_Rec_1028271,Human_Splice_Rec_1028288,Human_Splice_Rec_1028289 RMVar_hsa_circ_255274,RMVar_hsa_circ_74542,RMVar_hsa_circ_255277,RMVar_hsa_circ_255278,RMVar_hsa_circ_376812 101784 RMVar_ID_101784 Human_SNP_ID_387342105 m1A Human chr9 - 2506447 2506447 2506447 ACTCAGTGAGGGAGGAATTTTACTGACCCAGCATCCAGATGAACTTTGGTGAGGAGAGGAGGTGA ACTCAGTGAGGGAGGAATTTTACTGACCCAGCGTCCAGATGAACTTTGGTGAGGAGAGGAGGTGA T C VLDLR-AS1 Ensembl:ENSG00000236404 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:2506418..2506500 26863196 MeRIP-seq:(Medium) rs1468765957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5636466 Human_Splice_Rec_1028307,Human_Splice_Rec_1028325,Human_Splice_Rec_1028341,Human_Splice_Rec_1028357,Human_Splice_Rec_1028373,Human_Splice_Rec_1028395,Human_Splice_Rec_1028413,Human_Splice_Rec_1028429,Human_Splice_Rec_1028441,Human_Splice_Rec_1028457 RMVar_hsa_circ_255281,RMVar_hsa_circ_311247,RMVar_hsa_circ_332687,RMVar_hsa_circ_255280,RMVar_hsa_circ_339082,RMVar_hsa_circ_312078,RMVar_hsa_circ_303687,RMVar_hsa_circ_255283,RMVar_hsa_circ_255285,RMVar_hsa_circ_255286,RMVar_hsa_circ_255284,RMVar_hsa_circ_255282,RMVar_hsa_circ_255291,RMVar_hsa_circ_255289,RMVar_hsa_circ_255290,RMVar_hsa_circ_94710,RMVar_hsa_circ_69337,RMVar_hsa_circ_255292,RMVar_hsa_circ_255293,RMVar_hsa_circ_255294,RMVar_hsa_circ_33360 101785 RMVar_ID_101785 Human_SNP_ID_387377708 m1A Human chr9 - 2621775 2621775 2621775 GCGGCGGCCGGAGAGCGGGGTGAGCAGCGGGGAGGGGGCCGGAGGGGGCGTGGTCAACGGGAGGC GCGGCGGCCGGAGAGCGGGGTGAGCAGCGGGGGGGGGGCCGGAGGGGGCGTGGTCAACGGGAGGC T C VLDLR-AS1 Ensembl:ENSG00000236404 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2621609..2621840 26863196 MeRIP-seq:(Medium) rs1187720214 Functional Loss SNV dbSNP153 33..33 33 - - - 101786 RMVar_ID_101786 Human_SNP_ID_387446273 m1A Human chr9 - 2828780 2828780 2828780 TTTAGAGGGGTTTGATTGTTTTGTTTTGTTGCAGTCAGCAGATCACCGAACTCTGGACAAAGTGT TTTAGAGGGGTTTGATTGTTTTGTTTTGTTGCGGTCAGCAGATCACCGAACTCTGGACAAAGTGT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:2828754..2829946 32194978 MeRIP-seq:(Medium) rs1389778603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3205983,Human_RBP_ID_7920145,Human_RBP_ID_22339522 RMVar_hsa_circ_2306,RMVar_hsa_circ_92379,RMVar_hsa_circ_255307,RMVar_hsa_circ_268320,RMVar_hsa_circ_47545,RMVar_hsa_circ_371651,RMVar_hsa_circ_255315,RMVar_hsa_circ_62996,RMVar_hsa_circ_255316,RMVar_hsa_circ_116853,RMVar_hsa_circ_318915,RMVar_hsa_circ_333434,RMVar_hsa_circ_255318,RMVar_hsa_circ_255319,RMVar_hsa_circ_85031,RMVar_hsa_circ_371507,RMVar_hsa_circ_276272,RMVar_hsa_circ_255320,RMVar_hsa_circ_352619,RMVar_hsa_circ_64380 101787 RMVar_ID_101787 Human_SNP_ID_387449091 m1A Human chr9 - 2837320 2837320 2837320 TGGACCTAAAGTCACATCTAGGAACTTTGAGAAAAGTATCACAAAACTTGGGAAAAAGGGTGTAA TGGACCTAAAGTCACATCTAGGAACTTTGAGAGAAGTATCACAAAACTTGGGAAAAAGGGTGTAA T C PUM3 Ensembl:ENSG00000080608 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2837270..2838551 26863196 MeRIP-seq:(Medium) rs1325610022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90220,Human_RBP_ID_3206034,Human_RBP_ID_16651283 Human_Splice_Rec_1028576 RMVar_hsa_circ_268320,RMVar_hsa_circ_255316,RMVar_hsa_circ_116853,RMVar_hsa_circ_318915,RMVar_hsa_circ_333434,RMVar_hsa_circ_255318,RMVar_hsa_circ_371507,RMVar_hsa_circ_255321,RMVar_hsa_circ_276272,RMVar_hsa_circ_255320,RMVar_hsa_circ_358085,RMVar_hsa_circ_255323,RMVar_hsa_circ_354863,RMVar_hsa_circ_361956,RMVar_hsa_circ_54349,RMVar_hsa_circ_309706 101788 RMVar_ID_101788 Human_SNP_ID_387449485 m1A Human chr9 - 2838519 2838519 2838519 GTGATTGTTTTTGGTTTTGGTTTTGGTTTTCCAGAGTTGCTACGATGGAAGTTAAAGGGAAAAAG GTGATTGTTTTTGGTTTTGGTTTTGGTTTTCCGGAGTTGCTACGATGGAAGTTAAAGGGAAAAAG T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:2838476..2838525 26863196 MeRIP-seq:(Medium) rs779153747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92285,Human_RBP_ID_7920190 Human_Splice_Rec_1028575 101789 RMVar_ID_101789 Human_SNP_ID_387451351 m1A Human chr9 + 2843956 2843956 2843956 CCAGAAAGAGGCCAGAGGAGACTGCCCAGTGGACAACAGCCCCGAGAGACCTTCCCGACTTCCAG CCAGAAAGAGGCCAGAGGAGACTGCCCAGTGGGCAACAGCCCCGAGAGACCTTCCCGACTTCCAG A G lnc-KCNV2-1 RNACentral:URS00008BF3BE lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:2843952..2844098 26863196 MeRIP-seq:(Medium) rs943595412 Functional Loss SNV dbSNP153 33..33 33 - - - 101790 RMVar_ID_101790 Human_SNP_ID_387997073 m1A Human chr9 + 4490613 4490613 4490613 GCACCCGCATCTCGCCGCGCCGCCGAGCAGCCAGCAGTCCCCGGGTCGCCCAGCCCACGCGCGCA GCACCCGCATCTCGCCGCGCCGCCGAGCAGCCGGCAGTCCCCGGGTCGCCCAGCCCACGCGCGCA A G SLC1A1 Ensembl:ENSG00000106688 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:4490497..4490673 26863196 MeRIP-seq:(Medium) rs1433935079 Functional Loss SNV dbSNP153 33..33 33 - - - 101791 RMVar_ID_101791 Human_SNP_ID_387997077 m1A Human chr9 - 4490626 4490626 4490626 CTGGGCTCGGCCGTGCGCGCGTGGGCTGGGCGACCCGGGGACTGCTGGCTGCTCGGCGGCGCGGC CTGGGCTCGGCCGTGCGCGCGTGGGCTGGGCGTCCCGGGGACTGCTGGCTGCTCGGCGGCGCGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:4490576..4490700 26863196 MeRIP-seq:(Medium) rs1207223884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255400 101792 RMVar_ID_101792 Human_SNP_ID_387997078 m1A Human chr9 - 4490626 4490626 4490626 CTGGGCTCGGCCGTGCGCGCGTGGGCTGGGCGACCCGGGGACTGCTGGCTGCTCGGCGGCGCGGC CTGGGCTCGGCCGTGCGCGCGTGGGCTGGGCGGCCCGGGGACTGCTGGCTGCTCGGCGGCGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:4490576..4490700 26863196 MeRIP-seq:(Medium) rs1207223884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255400 101793 RMVar_ID_101793 Human_SNP_ID_388053366 m1A Human chr9 + 4662394 4662394 4662394 GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGAGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGCGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT A C PLPP6 Ensembl:ENSG00000205808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:4662345..4662664 26863196 MeRIP-seq:(Medium) rs34250374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035617 101794 RMVar_ID_101794 Human_SNP_ID_388053367 m1A Human chr9 + 4662394 4662394 4662394 GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGAGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGGGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT A G PLPP6 Ensembl:ENSG00000205808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:4662345..4662664 26863196 MeRIP-seq:(Medium) rs34250374 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5035617 101795 RMVar_ID_101795 Human_SNP_ID_388068471 m1A Human chr9 - 4711402 4711402 4711402 GAAACACTTCATTCTTTATAAAACTTTCTATAATGCCTTATTTGAATGTTAATCTTATGTGCTTT GAAACACTTCATTCTTTATAAAACTTTCTATAGTGCCTTATTTGAATGTTAATCTTATGTGCTTT T C AK3 Ensembl:ENSG00000147853 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:4711351..4711451 32194978 MeRIP-seq:(Medium) rs1250835663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929108,Human_RBP_ID_8952409,Human_RBP_ID_17322300,Human_RBP_ID_17549905,Human_RBP_ID_18136548 Human_miRNA_ID_2119527,Human_miRNA_ID_2122742,Human_miRNA_ID_2125959,Human_miRNA_ID_2129180,Human_miRNA_ID_2879482 RMVar_hsa_circ_255435,RMVar_hsa_circ_87153 101796 RMVar_ID_101796 Human_SNP_ID_388074281 m1A Human chr9 - 4727310 4727310 4727310 TTCAATGTAAACGAAACAGCCTTCTATTGGAAAAAGATGCCATCTAGGACTTCCATTGCTGGAGA TTCAATGTAAACGAAACAGCCTTCTATTGGAAGAAGATGCCATCTAGGACTTCCATTGCTGGAGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4500134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3216000 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 101797 RMVar_ID_101797 Human_SNP_ID_388076843 m1A Human chr9 - 4733610 4733610 4733610 AACAGGAACTCTTTCTGGATGCTTCACTGAAGAGGAGAGAGATTGAGTGATGGTGAGCGGGAGGA AACAGGAACTCTTTCTGGATGCTTCACTGAAGGGGAGAGAGATTGAGTGATGGTGAGCGGGAGGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:4733608..4733820 26863196 MeRIP-seq:(Medium) rs970335362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3216035,Human_RBP_ID_16683515,Human_RBP_ID_24304297 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 101798 RMVar_ID_101798 Human_SNP_ID_388080137 m1A Human chr9 + 4741036 4741036 4741036 AGTGATGCGCGACGACACGGTGCCCTTGCCCGAGCCCGGGGCCCCCATGATCACCGCTCGCAGCA AGTGATGCGCGACGACACGGTGCCCTTGCCCGGGCCCGGGGCCCCCATGATCACCGCTCGCAGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:4718515..4741071 32194978 MeRIP-seq:(Medium) rs1307472474 Functional Loss SNV dbSNP153 33..33 33 - - - 101799 RMVar_ID_101799 Human_SNP_ID_388080138 m1A Human chr9 + 4741036 4741036 4741036 AGTGATGCGCGACGACACGGTGCCCTTGCCCGAGCCCGGGGCCCCCATGATCACCGCTCGCAGCA AGTGATGCGCGACGACACGGTGCCCTTGCCCGTGCCCGGGGCCCCCATGATCACCGCTCGCAGCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:4718515..4741071 32194978 MeRIP-seq:(Medium) rs1307472474 Functional Loss SNV dbSNP153 33..33 33 - - - 101800 RMVar_ID_101800 Human_SNP_ID_388080172 m1A Human chr9 + 4741078 4741078 4741078 CCCCATGATCACCGCTCGCAGCAGCCGCGCGGACGCCCCCATGGCCGCAGACTGAGGCCCGCACC CCCCATGATCACCGCTCGCAGCAGCCGCGCGGGCGCCCCCATGGCCGCAGACTGAGGCCCGCACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:4740926..4741280 26863196 MeRIP-seq:(Medium) rs11539608 Functional Loss SNV dbSNP153 33..33 33 - - - 101801 RMVar_ID_101801 Human_SNP_ID_388097904 m1A Human chr9 - 4793049 4793049 4793049 TCCGAAGAGACGTGAGCAGCCCGAGAGCGGCGACTTCGGACAGACGCGGGACTCGTGACTCCGAT TCCGAAGAGACGTGAGCAGCCCGAGAGCGGCGGCTTCGGACAGACGCGGGACTCGTGACTCCGAT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:4792953..4793070 26863410 MeRIP-seq:(Medium) rs761566825 Functional Loss SNV dbSNP153 33..33 33 - - - 101802 RMVar_ID_101802 Human_SNP_ID_388110235 m1A Human chr9 + 4829168 4829168 4829168 GAATACCCTTGGGCTCGATAGAGGTAGAAGCAAAGTGCTTAGTGTTAGAGAGCGTTTCTTGAGGA GAATACCCTTGGGCTCGATAGAGGTAGAAGCAGAGTGCTTAGTGTTAGAGAGCGTTTCTTGAGGA A G RCL1 Ensembl:ENSG00000120158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:4829166..4829339 26863196 MeRIP-seq:(Medium) rs1241908384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111338,RMVar_hsa_circ_255441,RMVar_hsa_circ_255442,RMVar_hsa_circ_280556,RMVar_hsa_circ_317203,RMVar_hsa_circ_331846,RMVar_hsa_circ_377812,RMVar_hsa_circ_255445,RMVar_hsa_circ_255446,RMVar_hsa_circ_255444,RMVar_hsa_circ_255447,RMVar_hsa_circ_255448 101803 RMVar_ID_101803 Human_SNP_ID_388112211 m1A Human chr9 + 4835077 4835077 4835077 AGAAAAGTGGGCCTGAGCAGAGGTGGCAGTGCACAGTGGTTCTAGGGAGTGGCAAGTAATGAAGT AGAAAAGTGGGCCTGAGCAGAGGTGGCAGTGCGCAGTGGTTCTAGGGAGTGGCAAGTAATGAAGT A G RCL1 Ensembl:ENSG00000120158 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:4835049..4835224 26863196 MeRIP-seq:(Medium) rs1377984525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111338,RMVar_hsa_circ_255442,RMVar_hsa_circ_317203,RMVar_hsa_circ_331846,RMVar_hsa_circ_377812,RMVar_hsa_circ_255445,RMVar_hsa_circ_255446,RMVar_hsa_circ_255448,RMVar_hsa_circ_112059,RMVar_hsa_circ_255449,RMVar_hsa_circ_344985,RMVar_hsa_circ_255450 101804 RMVar_ID_101804 Human_SNP_ID_388112696 m1A Human chr9 - 4836555 4836555 4836555 CCCACAGCCTGTCTTGCTCTACGGCCTCCAACACCTGCTCCCACCCAGATCCTGTCAGCACCTAG CCCACAGCCTGTCTTGCTCTACGGCCTCCAACTCCTGCTCCCACCCAGATCCTGTCAGCACCTAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:4836504..4836782 26863196 MeRIP-seq:(Medium) rs776135185 Functional Loss SNV dbSNP153 33..33 33 - - - 101805 RMVar_ID_101805 Human_SNP_ID_388120416 m1A Human chr9 + 4860271 4860271 4860271 CATTGGTTTCTCCAACCTTAGCAAGACCCTCAAGTGATAACCATCACAAGATAAGGCCCCAATGC CATTGGTTTCTCCAACCTTAGCAAGACCCTCACGTGATAACCATCACAAGATAAGGCCCCAATGC A C RCL1 Ensembl:ENSG00000120158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:4860223..4860324 32194978 MeRIP-seq:(Medium) rs374683358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1059430,Human_RBP_ID_18136599,Human_RBP_ID_22118640 RMVar_hsa_circ_98860,RMVar_hsa_circ_255446,RMVar_hsa_circ_255448,RMVar_hsa_circ_255449,RMVar_hsa_circ_255451,RMVar_hsa_circ_255455,RMVar_hsa_circ_255456,RMVar_hsa_circ_378449 101806 RMVar_ID_101806 Human_SNP_ID_388120637 m1A Human chr9 + 4860943 4860943 4860943 TGGGATGTTTTTATATTCCAGGTGTGCTGTACATTCTTATTTTATTTTCACAATAGCTCTGTGAT TGGGATGTTTTTATATTCCAGGTGTGCTGTACGTTCTTATTTTATTTTCACAATAGCTCTGTGAT A G RCL1 Ensembl:ENSG00000120158 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs295918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929526,Human_RBP_ID_8928771,Human_RBP_ID_18136603,Human_RBP_ID_21906399,Human_RBP_ID_23300268,Human_RBP_ID_24304417,Human_RBP_ID_24523781,Human_RBP_ID_26563974,Human_RBP_ID_27137167,Human_RBP_ID_27786111 Human_miRNA_ID_860133 GWAS_ID_13381,GWAS_ID_13382,GWAS_ID_13383,GWAS_ID_13384 RMVar_hsa_circ_255456 101807 RMVar_ID_101807 Human_SNP_ID_388159043 m1A Human chr9 - 4985149 4985149 4985149 GGCCACACCGTCTTCTCAACGCCGCGGGCGACACTGGCTTCGCCGCCCTGCTAGCTTCGAACTCA GGCCACACCGTCTTCTCAACGCCGCGGGCGACTCTGGCTTCGCCGCCCTGCTAGCTTCGAACTCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:4985104..4985344 26863196 MeRIP-seq:(Medium) rs953329584 Functional Loss SNV dbSNP153 33..33 33 - - - 101808 RMVar_ID_101808 Human_SNP_ID_388159044 m1A Human chr9 - 4985149 4985149 4985149 GGCCACACCGTCTTCTCAACGCCGCGGGCGACACTGGCTTCGCCGCCCTGCTAGCTTCGAACTCA GGCCACACCGTCTTCTCAACGCCGCGGGCGACGCTGGCTTCGCCGCCCTGCTAGCTTCGAACTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:4985104..4985344 26863196 MeRIP-seq:(Medium) rs953329584 Functional Loss SNV dbSNP153 33..33 33 - - - 101809 RMVar_ID_101809 Human_SNP_ID_388191786 m1A Human chr9 - 5093270 5093270 5093270 AGAGGTGATGTTTTTGGTAAACAGGTGGGGTAAGATTTGCCGAGTTCCTTTTACTTTTTGTAATA AGAGGTGATGTTTTTGGTAAACAGGTGGGGTAGGATTTGCCGAGTTCCTTTTACTTTTTGTAATA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:5093214..5093422 26863196 MeRIP-seq:(Medium) rs1445319751 Functional Loss SNV dbSNP153 33..33 33 - - - 101810 RMVar_ID_101810 Human_SNP_ID_388191789 m1A Human chr9 + 5093277 5093277 5093277 AAAAGTAAAAGGAACTCGGCAAATCTTACCCCACCTGTTTACCAAAAACATCACCTCTAGCATTA AAAAGTAAAAGGAACTCGGCAAATCTTACCCCGCCTGTTTACCAAAAACATCACCTCTAGCATTA A G JAK2 Ensembl:ENSG00000096968 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:5093226..5093407 26863196 MeRIP-seq:(Medium) rs934506664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182568,Human_RBP_ID_17436522 RMVar_hsa_circ_335183,RMVar_hsa_circ_56133,RMVar_hsa_circ_361960,RMVar_hsa_circ_62686,RMVar_hsa_circ_255478,RMVar_hsa_circ_367023,RMVar_hsa_circ_338702,RMVar_hsa_circ_26078,RMVar_hsa_circ_69880,RMVar_hsa_circ_255482,RMVar_hsa_circ_74629,RMVar_hsa_circ_81292 101811 RMVar_ID_101811 Human_SNP_ID_388276387 m1A Human chr9 - 5358221 5358221 5358221 TTCATAGACAAATGAAATCATGCTTACCAATCAAATCTCAAAGCACAGAATTATTGACTTGAATC TTCATAGACAAATGAAATCATGCTTACCAATCGAATCTCAAAGCACAGAATTATTGACTTGAATC T C PLGRKT Ensembl:ENSG00000107020 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:5358121..5358222 32194978 MeRIP-seq:(Medium) rs1563762862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929887,Human_RBP_ID_9236801 RMVar_hsa_circ_255483 101812 RMVar_ID_101812 Human_SNP_ID_388302434 m1A Human chr9 + 5437827 5437827 5437827 GCGCTGGTGCCGGGACCAGGCGACCGGTACGCAAACCTCCAGGCCCGGGCTCCTTTCGCCCGCTG GCGCTGGTGCCGGGACCAGGCGACCGGTACGCCAACCTCCAGGCCCGGGCTCCTTTCGCCCGCTG A C lnc-CD274-1 RNACentral:URS0000D5A3F2 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:5437706..5437836;chr9:5437724..5437841 26863196 MeRIP-seq:(Medium) rs1208226676 Functional Loss SNV dbSNP153 33..33 33 - - - 101813 RMVar_ID_101813 Human_SNP_ID_388427621 m1A Human chr9 + 5831006 5831006 5831006 TTCTGGACTTCCTGTAGTCCTGGGGCCAATGGAGGTTATGTGTTCAAGATAATCCCTGGAAGTAA TTCTGGACTTCCTGTAGTCCTGGGGCCAATGGCGGTTATGTGTTCAAGATAATCCCTGGAAGTAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:5830957..5831075;chr9:5830944..5832519 26863196 MeRIP-seq:(Medium) rs200898949 Functional Loss SNV dbSNP153 33..33 33 - - - 101814 RMVar_ID_101814 Human_SNP_ID_388428491 m1A Human chr9 - 5832926 5832926 5832926 GCGGCCGCGCCACCGCCGGAGAGGGAGGCCCGAGCGCAGGAGCCTCTGGTGGATGGGTGCAGCGG GCGGCCGCGCCACCGCCGGAGAGGGAGGCCCGGGCGCAGGAGCCTCTGGTGGATGGGTGCAGCGG T C ERMP1 Ensembl:ENSG00000099219 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:5832826..5833075 26863196 MeRIP-seq:(Medium) rs1338362231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035625,Human_RBP_ID_9354954,Human_RBP_ID_22466302,Human_RBP_ID_26361612 101815 RMVar_ID_101815 Human_SNP_ID_388483217 m1A Human chr9 - 6007339 6007339 6007339 GCTGCAGATGGAAGAGAAGTTCGCCAGCGGCCAGTACGGGGGCATCACCGAGTTCGTGGCGGACT GCTGCAGATGGAAGAGAAGTTCGCCAGCGGCCGGTACGGGGGCATCACCGAGTTCGTGGCGGACT T C KIAA2026 Ensembl:ENSG00000183354 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:6007290..6007503 32194978 MeRIP-seq:(Medium) rs767514520 Functional Loss SNV dbSNP153 33..33 33 - - - 101816 RMVar_ID_101816 Human_SNP_ID_388483387 m1A Human chr9 - 6007624 6007624 6007624 AAGGAGTGCCTCCTCGCTGGAGGACGCGGACGATCAGGAGGAAGAGATGGAGGCGATGGTGATCG AAGGAGTGCCTCCTCGCTGGAGGACGCGGACGGTCAGGAGGAAGAGATGGAGGCGATGGTGATCG T C KIAA2026 Ensembl:ENSG00000183354 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:6007448..6007854 26863196 MeRIP-seq:(Medium) rs984788210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23094296 101817 RMVar_ID_101817 Human_SNP_ID_388483393 m1A Human chr9 - 6007633 6007633 6007633 GGCCCACGGAAGGAGTGCCTCCTCGCTGGAGGACGCGGACGATCAGGAGGAAGAGATGGAGGCGA GGCCCACGGAAGGAGTGCCTCCTCGCTGGAGGGCGCGGACGATCAGGAGGAAGAGATGGAGGCGA T C KIAA2026 Ensembl:ENSG00000183354 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:6007351..6007901 26863196 MeRIP-seq:(Medium) rs775382538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23094296 101818 RMVar_ID_101818 Human_SNP_ID_388727515 m1A Human chr9 - 6758090 6758090 6758090 AAATTTGGGAGACTTGTTCCGCACTAGGTGACAGCTGTTCGCTGCGCACGCGCACAGGACCCCGG AAATTTGGGAGACTTGTTCCGCACTAGGTGACGGCTGTTCGCTGCGCACGCGCACAGGACCCCGG T C lnc-GLDC-6 RNACentral:URS0000D5A24F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:6757805..6758197 26863196 MeRIP-seq:(Medium) rs1212986798 Functional Loss SNV dbSNP153 33..33 33 - - - 101819 RMVar_ID_101819 Human_SNP_ID_388794503 m1A Human chr9 - 6949445 6949445 6949445 CTCCCAAAGTGCCGAGATTACAGCCTCTGCCCAGCCGCCACCCCGTCTGGGAAGTGAGGAACGTC CTCCCAAAGTGCCGAGATTACAGCCTCTGCCCGGCCGCCACCCCGTCTGGGAAGTGAGGAACGTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:6949344..6949471 26863196 MeRIP-seq:(Medium) rs1054579899 Functional Loss SNV dbSNP153 33..33 33 - - - 101820 RMVar_ID_101820 Human_SNP_ID_389075854 m1A Human chr9 + 7798575 7798575 7798575 AGACAGAAGACAGATTCACTGGTGGTACTTTCAAACAACGCGGTAGGCCTTCCCTTTGGGGTCTG AGACAGAAGACAGATTCACTGGTGGTACTTTCCAACAACGCGGTAGGCCTTCCCTTTGGGGTCTG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:7798551..7798575 26863196 MeRIP-seq:(Medium) rs1337611127 Functional Loss SNV dbSNP153 33..33 33 - - - 101821 RMVar_ID_101821 Human_SNP_ID_389076261 m1A Human chr9 - 7799524 7799519 7799524 GGGCGGGCGGGTACGTGTACTGGGTGGCACGGAAGCCCATGAAGATGGGATACCCCCCGAGTCCA GGGCGGGCGGGTACGTGTACTGGGTGGCACGG_____CATGAAGATGGGATACCCCCCGAGTCCA GGGCTT G DMAC1 Ensembl:ENSG00000137038 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:7799476..7799700 32194978 MeRIP-seq:(Medium) rs1160666389 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_5036663,Human_RBP_ID_5329450,Human_RBP_ID_17666459,Human_RBP_ID_22466032 Human_Splice_Rec_1030903 101822 RMVar_ID_101822 Human_SNP_ID_389076376 m1A Human chr9 + 7799711 7799711 7799711 GTACCGGGAGGCGCAGTGATATAGGACTCAAAAGGCTGGGACAACCGAGACCCCATGCTCTGGAA GTACCGGGAGGCGCAGTGATATAGGACTCAAATGGCTGGGACAACCGAGACCCCATGCTCTGGAA A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:7799660..7799748 26863410 MeRIP-seq:(Medium) rs772325105 Functional Loss SNV dbSNP153 33..33 33 - - - 101823 RMVar_ID_101823 Human_SNP_ID_389076401 m1A Human chr9 - 7799739 7799739 7799739 ACCAAAGACGCCCAAGGTTGAGGCCGAGTTCCAGAGCATGGGGTCTCGGTTGTCCCAGCCTTTTG ACCAAAGACGCCCAAGGTTGAGGCCGAGTTCCGGAGCATGGGGTCTCGGTTGTCCCAGCCTTTTG T C DMAC1 Ensembl:ENSG00000137038 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:7799601..7799775 26863196 MeRIP-seq:(Medium) rs200925039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_720463,Human_RBP_ID_1705884,Human_RBP_ID_5036099 101824 RMVar_ID_101824 Human_SNP_ID_390854301 m1A Human chr9 - 13119578 13119578 13119578 AGGAATTGCAGATGCCGATGGAAGACTGATGCAGGGAGACCAGATATTAATGGTGAATGGGGAAG AGGAATTGCAGATGCCGATGGAAGACTGATGCGGGGAGACCAGATATTAATGGTGAATGGGGAAG T C MPDZ Ensembl:ENSG00000107186 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:13109023..13119701 32194978 MeRIP-seq:(Medium) rs779043354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1031810,Human_Splice_Rec_1031811,Human_Splice_Rec_1031827,Human_Splice_Rec_1031914,Human_Splice_Rec_1031915,Human_Splice_Rec_1032002,Human_Splice_Rec_1032003,Human_Splice_Rec_1032058,Human_Splice_Rec_1032059,Human_Splice_Rec_1032088,Human_Splice_Rec_1032089,Human_Splice_Rec_1032130,Human_Splice_Rec_1032131,Human_Splice_Rec_1032178,Human_Splice_Rec_1032179,Human_Splice_Rec_1032226,Human_Splice_Rec_1032227,Human_Splice_Rec_1032314,Human_Splice_Rec_1032315,Human_Splice_Rec_1032400,Human_Splice_Rec_1032401,Human_Splice_Rec_1032438,Human_Splice_Rec_1032439,Human_Splice_Rec_1032532,Human_Splice_Rec_1032533,Human_Splice_Rec_1032554,Human_Splice_Rec_1032555 RMVar_hsa_circ_52340,RMVar_hsa_circ_63884,RMVar_hsa_circ_69191,RMVar_hsa_circ_74184 101825 RMVar_ID_101825 Human_SNP_ID_390860100 m1A Human chr9 + 13138018 13138018 13138018 GACCATCTTTTCCTGCAGCTCCATTTGGATCAATCCCCACTATGAAGACACTCATCCTGGATCGG GACCATCTTTTCCTGCAGCTCCATTTGGATCAGTCCCCACTATGAAGACACTCATCCTGGATCGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:13136753..13138057 32194978 MeRIP-seq:(Medium) rs1475254353 Functional Loss SNV dbSNP153 33..33 33 - - - 101826 RMVar_ID_101826 Human_SNP_ID_390860101 m1A Human chr9 + 13138018 13138018 13138018 GACCATCTTTTCCTGCAGCTCCATTTGGATCAATCCCCACTATGAAGACACTCATCCTGGATCGG GACCATCTTTTCCTGCAGCTCCATTTGGATCATTCCCCACTATGAAGACACTCATCCTGGATCGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:13136753..13138057 32194978 MeRIP-seq:(Medium) rs1475254353 Functional Loss SNV dbSNP153 33..33 33 - - - 101827 RMVar_ID_101827 Human_SNP_ID_390902591 m1A Human chr9 - 13279583 13279583 13279583 GGAGCGCTAGGCTGGCGTCGGGCCACCGCGGGATTAAGTTTCTCAGTCACGCGTGAGTGTCTGTG GGAGCGCTAGGCTGGCGTCGGGCCACCGCGGGGTTAAGTTTCTCAGTCACGCGTGAGTGTCTGTG T C MPDZ Ensembl:ENSG00000107186 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:13279546..13279638 26863196 MeRIP-seq:(Medium) rs1352497960 Functional Loss SNV dbSNP153 33..33 33 - - - 101828 RMVar_ID_101828 Human_SNP_ID_391195997 m1A Human chr9 - 14220710 14220710 14220710 CTTGATGAAGGGGGTTTTCTGAATGGGAAATAAGGGAGAGGGCAGGAGGAAGAGGAGAAAGTGAA CTTGATGAAGGGGGTTTTCTGAATGGGAAATACGGGAGAGGGCAGGAGGAAGAGGAGAAAGTGAA T G NFIB Ensembl:ENSG00000147862 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:14220610..14220727 26863196 MeRIP-seq:(Medium) rs1225349015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24294357 RMVar_hsa_circ_92502,RMVar_hsa_circ_255763,RMVar_hsa_circ_21878,RMVar_hsa_circ_353686,RMVar_hsa_circ_273008,RMVar_hsa_circ_12900,RMVar_hsa_circ_344759 101829 RMVar_ID_101829 Human_SNP_ID_391204584 m1A Human chr9 - 14248267 14248241 14248267 GGAGAGGGGAGGGCAGGGCAGTTTAGGTGGGAAGGAAGGAAGGGCAGTTTAGGTGGGAGGATTGC GGAGAGGGGAGGGCAGGGCAGTTTAGGTGGGA__________________________GGATTGC CTCCCACCTAAACTGCCCTTCCTTCCT C NFIB Ensembl:ENSG00000147862 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:14248181..14248303 26863196 MeRIP-seq:(Medium) rs1212220508 Functional Loss DEL dbSNP153 33..58 33 - - - Human_RBP_ID_7909900 RMVar_hsa_circ_92502,RMVar_hsa_circ_255763,RMVar_hsa_circ_21878,RMVar_hsa_circ_353686,RMVar_hsa_circ_273008,RMVar_hsa_circ_12900,RMVar_hsa_circ_344759,RMVar_hsa_circ_255778,RMVar_hsa_circ_255775 101830 RMVar_ID_101830 Human_SNP_ID_391209824 m1A Human chr9 - 14266698 14266698 14266698 GAGGGAGGAGGGGAAGATGACTGCATCACTGAATCAATGCTGAGATGGGCCACAAAAATGGGGCA GAGGGAGGAGGGGAAGATGACTGCATCACTGAGTCAATGCTGAGATGGGCCACAAAAATGGGGCA T C NFIB Ensembl:ENSG00000147862 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:14266670..14266765 26863196 MeRIP-seq:(Medium) rs1229165704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92502,RMVar_hsa_circ_255763,RMVar_hsa_circ_21878,RMVar_hsa_circ_353686,RMVar_hsa_circ_273008,RMVar_hsa_circ_12900,RMVar_hsa_circ_344759,RMVar_hsa_circ_255778,RMVar_hsa_circ_255775 101831 RMVar_ID_101831 Human_SNP_ID_391210333 m1A Human chr9 - 14268409 14268409 14268409 GGAGGGTGACTAGACTTTAGCCTGTGTAGGCGAAGTGGAGGAGAGTTGTAAGAGACTAGGCTGAA GGAGGGTGACTAGACTTTAGCCTGTGTAGGCGGAGTGGAGGAGAGTTGTAAGAGACTAGGCTGAA T C NFIB Ensembl:ENSG00000147862 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:14268387..14268532 26863196 MeRIP-seq:(Medium) rs1191957421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92502,RMVar_hsa_circ_255763,RMVar_hsa_circ_21878,RMVar_hsa_circ_353686,RMVar_hsa_circ_273008,RMVar_hsa_circ_12900,RMVar_hsa_circ_344759,RMVar_hsa_circ_255775 101832 RMVar_ID_101832 Human_SNP_ID_391210342 m1A Human chr9 + 14268435 14268435 14268435 TCCACTTCGCCTACACAGGCTAAAGTCTAGTCACCCTCCCCTGATGGTTCATGACCCCCAACTAC TCCACTTCGCCTACACAGGCTAAAGTCTAGTCTCCCTCCCCTGATGGTTCATGACCCCCAACTAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:14268389..14268599 26863196 MeRIP-seq:(Medium) rs926268379 Functional Loss SNV dbSNP153 33..33 33 - - - 101833 RMVar_ID_101833 Human_SNP_ID_391223569 m1A Human chr9 - 14314092 14314083 14314093 CCCTCGCGCACACACATGGTCGGCTCGCGGCAAAGTTTCGCCTGCGATCACCACTCCGGGATCCT CCCTCGCGCACACACATGGTCGGCTCGCGGC__________CTGCGATCACCACTCCGGGATCCT GGCGAAACTTT G NFIB Ensembl:ENSG00000147862 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:14314047..14314140 26863196 MeRIP-seq:(Medium) rs1204066267 Functional Loss DEL dbSNP153 32..41 33 - - - 101834 RMVar_ID_101834 Human_SNP_ID_391223575 m1A Human chr9 - 14314092 14314092 14314092 CCCTCGCGCACACACATGGTCGGCTCGCGGCAAAGTTTCGCCTGCGATCACCACTCCGGGATCCT CCCTCGCGCACACACATGGTCGGCTCGCGGCAGAGTTTCGCCTGCGATCACCACTCCGGGATCCT T C NFIB Ensembl:ENSG00000147862 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:14314047..14314140 26863196 MeRIP-seq:(Medium) rs980945408 Functional Loss SNV dbSNP153 33..33 33 - - - 101835 RMVar_ID_101835 Human_SNP_ID_391223641 m1A Human chr9 + 14314225 14314225 14314225 GATGGGGGAGAAGGGAGAGGCCGGGGTGAGGGAGGGGGCGCGAGCGCTGATCTCTGGGGCGGAAG GATGGGGGAGAAGGGAGAGGCCGGGGTGAGGGGGGGGGCGCGAGCGCTGATCTCTGGGGCGGAAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:14313693..14314600 26863196 MeRIP-seq:(Medium) rs1455877544 Functional Loss SNV dbSNP153 33..33 33 - - - 101836 RMVar_ID_101836 Human_SNP_ID_391223932 m1A Human chr9 - 14314899 14314899 14314899 CTCGGATGTTCCCGCGGCTTAAAAGAGTCCGCAGCGAGCACCGAAATACCTCTTCCAGGGCGGGT CTCGGATGTTCCCGCGGCTTAAAAGAGTCCGCCGCGAGCACCGAAATACCTCTTCCAGGGCGGGT T G NFIB Ensembl:ENSG00000147862 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:14314852..14314997 26863196 MeRIP-seq:(Medium) rs148601146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5023617 101837 RMVar_ID_101837 Human_SNP_ID_391315046 m1A Human chr9 + 14618970 14618970 14618970 GACCCATCTGTGCCCACCATCCATCTGTTTAGACATGATTGGCAAAGTGGTAGGGAACTCGCAGT GACCCATCTGTGCCCACCATCCATCTGTTTAGCCATGATTGGCAAAGTGGTAGGGAACTCGCAGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:14618920..14619009 32194978 MeRIP-seq:(Medium) rs1346934237 Functional Loss SNV dbSNP153 33..33 33 - - - 101838 RMVar_ID_101838 Human_SNP_ID_391410977 m1A Human chr9 - 14921829 14921829 14921829 TATTGGAAGTGGTTGCAATCTGGATTCAGCCCAATTCCGTTACCTGATGGGGGAAAGGCTGGGAG TATTGGAAGTGGTTGCAATCTGGATTCAGCCCGATTCCGTTACCTGATGGGGGAAAGGCTGGGAG T C CLCN3P1,LDHAP4 Ensembl:ENSG00000232000,Ensembl:ENSG00000214110 Pseudogene,Pseudogene exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs555929180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_964532,Human_RBP_ID_1708134,Human_RBP_ID_3911117,Human_RBP_ID_5229613,Human_RBP_ID_9264791,Human_RBP_ID_10440581,Human_RBP_ID_17322827,Human_RBP_ID_17579765,Human_RBP_ID_17674183,Human_RBP_ID_18140442,Human_RBP_ID_18427719,Human_RBP_ID_18508051,Human_RBP_ID_22466033,Human_RBP_ID_22530896,Human_RBP_ID_22776414,Human_RBP_ID_24392183 Human_miRNA_ID_1835091 101839 RMVar_ID_101839 Human_SNP_ID_37261780 m1A Human chr1 - 165652541 165652541 165652541 ATCCCACTCCACATCCCCTTTCCACCTTCCCCACTTTGTTTTCTTCTCTGCACTCACCACCTCCT ATCCCACTCCACATCCCCTTTCCACCTTCCCCGCTTTGTTTTCTTCTCTGCACTCACCACCTCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:165652532..165652683 26863196 MeRIP-seq:(Medium) rs4147602 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - GWAS_ID_13385,GWAS_ID_13386 101840 RMVar_ID_101840 Human_SNP_ID_37273195 m1A Human chr1 - 165698486 165698486 165698486 TTCGCAGTCTTCGGCCCTCTCCTGTCGCCGCCATGAGCACTGGCACCTTCGTCGTGTCGCAGCCG TTCGCAGTCTTCGGCCCTCTCCTGTCGCCGCCTTGAGCACTGGCACCTTCGTCGTGTCGCAGCCG T A ALDH9A1 Ensembl:ENSG00000143149 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:165698436..165698522 26863196 MeRIP-seq:(Medium) rs774846915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331145,Human_RBP_ID_4005169,Human_RBP_ID_5433142,Human_RBP_ID_5456572,Human_RBP_ID_18555021,Human_RBP_ID_26799131 101841 RMVar_ID_101841 Human_SNP_ID_37273196 m1A Human chr1 - 165698486 165698486 165698486 TTCGCAGTCTTCGGCCCTCTCCTGTCGCCGCCATGAGCACTGGCACCTTCGTCGTGTCGCAGCCG TTCGCAGTCTTCGGCCCTCTCCTGTCGCCGCCGTGAGCACTGGCACCTTCGTCGTGTCGCAGCCG T C ALDH9A1 Ensembl:ENSG00000143149 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:165698436..165698522 26863196 MeRIP-seq:(Medium) rs774846915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331145,Human_RBP_ID_4005169,Human_RBP_ID_5433142,Human_RBP_ID_5456572,Human_RBP_ID_18555021,Human_RBP_ID_26799131 101842 RMVar_ID_101842 Human_SNP_ID_37280486 m1A Human chr1 - 165727183 165727183 165727183 GGCACTCTTAGATCTCCCTTGGAGACAAGGTTATAGTTATATGTTGTTAATCTCGCAGAGCTTCC GGCACTCTTAGATCTCCCTTGGAGACAAGGTTGTAGTTATATGTTGTTAATCTCGCAGAGCTTCC T C TMCO1 Ensembl:ENSG00000143183 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:165727034..165727184 32194978 MeRIP-seq:(Medium) rs549844361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331183,Human_RBP_ID_3285028,Human_RBP_ID_8289009,Human_RBP_ID_27580503 101843 RMVar_ID_101843 Human_SNP_ID_37290127 m1A Human chr1 - 165768179 165768179 165768179 GGAAAAACAGAGTAAAAAATGTGAGTATGGCAACACATTAGAAATAATTTCAACACGTCAAGCTC GGAAAAACAGAGTAAAAAATGTGAGTATGGCAGCACATTAGAAATAATTTCAACACGTCAAGCTC T C TMCO1 Ensembl:ENSG00000143183 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:165768176..165768275;chr1:165768176..165768225 26863196 MeRIP-seq:(Medium) rs146699918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22637769 Human_Splice_Rec_153346,Human_Splice_Rec_153358,Human_Splice_Rec_153370,Human_Splice_Rec_153386,Human_Splice_Rec_153398,Human_Splice_Rec_153410,Human_Splice_Rec_153420,Human_Splice_Rec_153430,Human_Splice_Rec_153442 RMVar_hsa_circ_68955,RMVar_hsa_circ_74194 101844 RMVar_ID_101844 Human_SNP_ID_37290329 m1A Human chr1 + 165768784 165768783 165768784 CTCGCACCTTCGTCTCTGCACTCTCACCCGCCAGGGGGAAAGCGCTCTACAGCCAGGAAAAGTGA CTCGCACCTTCGTCTCTGCACTCTCACCCGCC_GGGGGAAAGCGCTCTACAGCCAGGAAAAGTGA CA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:165768676..165768825 32194978 MeRIP-seq:(Medium) rs1197771764 Functional Loss DEL dbSNP153 33..33 33 - - - 101845 RMVar_ID_101845 Human_SNP_ID_37290330 m1A Human chr1 + 165768784 165768784 165768784 CTCGCACCTTCGTCTCTGCACTCTCACCCGCCAGGGGGAAAGCGCTCTACAGCCAGGAAAAGTGA CTCGCACCTTCGTCTCTGCACTCTCACCCGCCCGGGGGAAAGCGCTCTACAGCCAGGAAAAGTGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:165768676..165768825 32194978 MeRIP-seq:(Medium) rs906155551 Functional Loss SNV dbSNP153 33..33 33 - - - 101846 RMVar_ID_101846 Human_SNP_ID_37290342 m1A Human chr1 + 165768802 165768802 165768802 CACTCTCACCCGCCAGGGGGAAAGCGCTCTACAGCCAGGAAAAGTGAAGCGAAAACGGCTTCCGT CACTCTCACCCGCCAGGGGGAAAGCGCTCTACCGCCAGGAAAAGTGAAGCGAAAACGGCTTCCGT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:165768701..165768850 26863410 MeRIP-seq:(Medium) rs750014669 Functional Loss SNV dbSNP153 33..33 33 - - - 101847 RMVar_ID_101847 Human_SNP_ID_37304589 m1A Human chr1 + 165827671 165827671 165827671 AAAGGAAGGCTCTTGGCTCCTTCGGGAAACCCAGCCCCGTCACCGGGCTCCGAGCGGCTCGCAGG AAAGGAAGGCTCTTGGCTCCTTCGGGAAACCCTGCCCCGTCACCGGGCTCCGAGCGGCTCGCAGG A T UCK2 Ensembl:ENSG00000143179 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:165827626..165827950 26863196 MeRIP-seq:(Medium) rs961407294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074572,Human_RBP_ID_5433146,Human_RBP_ID_26799133 101848 RMVar_ID_101848 Human_SNP_ID_37304645 m1A Human chr1 + 165827815 165827815 165827815 GGGAGCGTGCGTCCGTTCGCACAGGCAGCGGGAGGAGGGGCGGCGCGAACCATGGCCGGGGACAG GGGAGCGTGCGTCCGTTCGCACAGGCAGCGGGTGGAGGGGCGGCGCGAACCATGGCCGGGGACAG A T UCK2 Ensembl:ENSG00000143179 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:165827532..165827973;chr1:165827541..165890325;chr1:165827551..165890250 26863196 MeRIP-seq:(Medium) rs1359877023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25014,Human_RBP_ID_224048,Human_RBP_ID_4005292,Human_RBP_ID_19215532 101849 RMVar_ID_101849 Human_SNP_ID_37319798 m1A Human chr1 - 165890166 165890166 165890166 AGGAGAGAAGAGAGCACCCAGGAATAAGAGAAAGGGCACGTGTGGTACAGAGGAAGTCCCGAGAG AGGAGAGAAGAGAGCACCCAGGAATAAGAGAACGGGCACGTGTGGTACAGAGGAAGTCCCGAGAG T G AL358115.1 Ensembl:ENSG00000236364 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:165890161..165890375 26863196 MeRIP-seq:(Medium) rs1306963855 Functional Loss SNV dbSNP153 33..33 33 - - - 101850 RMVar_ID_101850 Human_SNP_ID_37319826 m1A Human chr1 + 165890256 165890256 165890256 CGTGCAGCTCCTGGGGCAGAATGAGGTGGACTATCGCCAGAAGCAGGTGGTCATCCTGAGCCAGG CGTGCAGCTCCTGGGGCAGAATGAGGTGGACTGTCGCCAGAAGCAGGTGGTCATCCTGAGCCAGG A G UCK2 Ensembl:ENSG00000143179 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:165890201..165890275 32194978 MeRIP-seq:(Medium) rs1269500147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_972415,Human_RBP_ID_1250965,Human_RBP_ID_1414724,Human_RBP_ID_1728240,Human_RBP_ID_3936968,Human_RBP_ID_4005319,Human_RBP_ID_5705825,Human_RBP_ID_8289148,Human_RBP_ID_8737111,Human_RBP_ID_18187834,Human_RBP_ID_21880667,Human_RBP_ID_23341427 Human_Splice_Rec_153450,Human_Splice_Rec_153464 RMVar_hsa_circ_137294,RMVar_hsa_circ_107607,RMVar_hsa_circ_137291,RMVar_hsa_circ_137292,RMVar_hsa_circ_275884,RMVar_hsa_circ_376786,RMVar_hsa_circ_376865,RMVar_hsa_circ_276159,RMVar_hsa_circ_271898,RMVar_hsa_circ_137296,RMVar_hsa_circ_137298,RMVar_hsa_circ_99799,RMVar_hsa_circ_137299,RMVar_hsa_circ_137297,RMVar_hsa_circ_137295,RMVar_hsa_circ_137293 101851 RMVar_ID_101851 Human_SNP_ID_37320436 m1A Human chr1 - 165892892 165892892 165892892 CCTCCACACCTCTCCACTGCCATGCCCCAACCAAGCTGATCCATGCCTAGCTCTGAAATGCTTCC CCTCCACACCTCTCCACTGCCATGCCCCAACCCAGCTGATCCATGCCTAGCTCTGAAATGCTTCC T G AL358115.1 Ensembl:ENSG00000236364 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:165892887..165892998;chr1:165892891..165893110 26863196 MeRIP-seq:(Medium) rs1479402249 Functional Loss SNV dbSNP153 33..33 33 - - - 101852 RMVar_ID_101852 Human_SNP_ID_37323992 m1A Human chr1 - 165907762 165907762 165907762 CCTGCCTCTTGCGTGAAGGGGTGTAGCCGTTGAGACAGCCATTGGTCTGCCGTTTGGAGGGCCCT CCTGCCTCTTGCGTGAAGGGGTGTAGCCGTTGGGACAGCCATTGGTCTGCCGTTTGGAGGGCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:165907711..165907795 26863196 MeRIP-seq:(Medium) rs1420376344 Functional Loss SNV dbSNP153 33..33 33 - - - 101853 RMVar_ID_101853 Human_SNP_ID_37324157 m1A Human chr1 - 165908252 165908252 165908252 TAGCCACCCTCCCTGTCTCTCACAGATGCCCGAGCCTCCCCACCCTGGGACACAACAGGCAATTT TAGCCACCCTCCCTGTCTCTCACAGATGCCCGGGCCTCCCCACCCTGGGACACAACAGGCAATTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:165908203..165908288 26863196 MeRIP-seq:(Medium) rs1480379110 Functional Loss SNV dbSNP153 33..33 33 - - - 101854 RMVar_ID_101854 Human_SNP_ID_37555703 m1A Human chr1 - 166839587 166839587 166839587 CCCGCGCGCACTCACCGCCGGGCCCAGCGGCCAGGGCGCGGGGTGGGGACGCGAGGGCTCCGGCC CCCGCGCGCACTCACCGCCGGGCCCAGCGGCCGGGGCGCGGGGTGGGGACGCGAGGGCTCCGGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:166839488..166839729 26863196 MeRIP-seq:(Medium) rs1460817603 Functional Loss SNV dbSNP153 33..33 33 - - - 101855 RMVar_ID_101855 Human_SNP_ID_37558313 m1A Human chr1 - 166850348 166850348 166850348 CACAATCTTTTGGTGGTTCTCCTCCTCCTGGCAACTCACTCTCGATTTCCCACAGGACATCGTCT CACAATCTTTTGGTGGTTCTCCTCCTCCTGGCGACTCACTCTCGATTTCCCACAGGACATCGTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:166850299..166850416 26863196 MeRIP-seq:(Medium) rs142458414 Functional Loss SNV dbSNP153 33..33 33 - - - 101856 RMVar_ID_101856 Human_SNP_ID_37558502 m1A Human chr1 + 166851047 166851047 166851047 GAGCTGCCAGAACATCTGAGAGCTGTAAAGTTAAAATTATTTGGACCCAAAGAAGCATAGTCTGA GAGCTGCCAGAACATCTGAGAGCTGTAAAGTTTAAATTATTTGGACCCAAAGAAGCATAGTCTGA A T POGK Ensembl:ENSG00000143157 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3820387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1728333,Human_RBP_ID_5706642,Human_RBP_ID_8737276,Human_RBP_ID_10636475,Human_RBP_ID_17331159,Human_RBP_ID_18218873,Human_RBP_ID_27580682 GWAS_ID_13387,GWAS_ID_13388 RMVar_hsa_circ_137310 101857 RMVar_ID_101857 Human_SNP_ID_37564486 m1A Human chr1 + 166876223 166876223 166876223 AGTTCTTCTTGGCCGCCTCCAGCTCGCTCACAAAGGTCGCCATTGCTCCGCGTGTCTCAGCCCGA AGTTCTTCTTGGCCGCCTCCAGCTCGCTCACATAGGTCGCCATTGCTCCGCGTGTCTCAGCCCGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:166876136..166876268 26863196 MeRIP-seq:(Medium) rs903780388 Functional Loss SNV dbSNP153 33..33 33 - - - 101858 RMVar_ID_101858 Human_SNP_ID_37586435 m1A Human chr1 - 166975479 166975465 166975480 GGCATGCGGATGCGCCGCCGAGCGCTGCGCGGACCCCGGAAGCCCGCGGCAGCGCGCGCTCAGCC GGCATGCGGATGCGCCGCCGAGCGCTGCGCG_______________CGGCAGCGCGCGCTCAGCC GCGGGCTTCCGGGGTC G ILDR2 Ensembl:ENSG00000143195 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:166975378..166975534 26863410 MeRIP-seq:(Medium) rs1201324990 Functional Loss DEL dbSNP153 32..46 33 - - - 101859 RMVar_ID_101859 Human_SNP_ID_37586447 m1A Human chr1 - 166975479 166975479 166975479 GGCATGCGGATGCGCCGCCGAGCGCTGCGCGGACCCCGGAAGCCCGCGGCAGCGCGCGCTCAGCC GGCATGCGGATGCGCCGCCGAGCGCTGCGCGGGCCCCGGAAGCCCGCGGCAGCGCGCGCTCAGCC T C ILDR2 Ensembl:ENSG00000143195 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:166975378..166975534 26863410 MeRIP-seq:(Medium) rs1163601619 Functional Loss SNV dbSNP153 33..33 33 - - - 101860 RMVar_ID_101860 Human_SNP_ID_37654343 m1A Human chr1 + 167249544 167249544 167249544 GGAACAGAAGGACAGGGGAGCAAGGGAGTGGAAAGTCTTGACAGGAATGTCATTCATGGACCCTG GGAACAGAAGGACAGGGGAGCAAGGGAGTGGAGAGTCTTGACAGGAATGTCATTCATGGACCCTG A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:167249542..167249727 26863196 MeRIP-seq:(Medium) rs1455843451 Functional Loss SNV dbSNP153 33..33 33 - - - 101861 RMVar_ID_101861 Human_SNP_ID_37660753 m1A Human chr1 - 167276791 167276791 167276791 CATACTTATTGATTTTCTCCTTTGCCTTTCCCACCCTTATTTGATGACAATATGGAACTGAAAAT CATACTTATTGATTTTCTCCTTTGCCTTTCCCCCCCTTATTTGATGACAATATGGAACTGAAAAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:167276783..167276916 26863196 MeRIP-seq:(Medium) rs1378846973 Functional Loss SNV dbSNP153 33..33 33 - - - 101862 RMVar_ID_101862 Human_SNP_ID_37660764 m1A Human chr1 + 167276836 167276836 167276836 GGAGAAAATCAATAAGTATGGAGAAGAAAGAAATGAGTAGATAGAACAAAAAAGATGAGAAAGGA GGAGAAAATCAATAAGTATGGAGAAGAAAGAAGTGAGTAGATAGAACAAAAAAGATGAGAAAGGA A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:167276833..167276916 26863196 MeRIP-seq:(Medium) rs570558876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10638850 RMVar_hsa_circ_137324 101863 RMVar_ID_101863 Human_SNP_ID_37682196 m1A Human chr1 + 167365418 167365418 167365418 GATGAATGTTGGTAACTGAAATCTAGTGCTTTATTTCATTTATTTCTTTTAATAGTTGAAATTAT GATGAATGTTGGTAACTGAAATCTAGTGCTTTGTTTCATTTATTTCTTTTAATAGTTGAAATTAT A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:167365405..167365495 26863196 MeRIP-seq:(Medium) rs775820178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5707594 RMVar_hsa_circ_32153,RMVar_hsa_circ_55036,RMVar_hsa_circ_352709,RMVar_hsa_circ_284123,RMVar_hsa_circ_318828,RMVar_hsa_circ_329303,RMVar_hsa_circ_367912,RMVar_hsa_circ_71056,RMVar_hsa_circ_137326,RMVar_hsa_circ_137327,RMVar_hsa_circ_137328,RMVar_hsa_circ_92690 101864 RMVar_ID_101864 Human_SNP_ID_37693206 m1A Human chr1 + 167412026 167412026 167412026 GTGATTTCCACAGCGCCTCCAGCTTCCTCAGCAGTCACGTCCCCCTCTCTGAGTCCCTCCCCTTC GTGATTTCCACAGCGCCTCCAGCTTCCTCAGCGGTCACGTCCCCCTCTCTGAGTCCCTCCCCTTC A G POU2F1 Ensembl:ENSG00000143190 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:167411975..167412058 26863196 MeRIP-seq:(Medium) rs368963193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8737373,Human_RBP_ID_17213519,Human_RBP_ID_18930217,Human_RBP_ID_27390778 Human_Splice_Rec_154010,Human_Splice_Rec_154042,Human_Splice_Rec_154104,Human_Splice_Rec_154148,Human_Splice_Rec_154180,Human_Splice_Rec_154214,Human_Splice_Rec_154244,Human_Splice_Rec_154272,Human_Splice_Rec_154308 Human_miRNA_ID_2036204,Human_miRNA_ID_2346903 RMVar_hsa_circ_367912,RMVar_hsa_circ_103017,RMVar_hsa_circ_137330,RMVar_hsa_circ_14334,RMVar_hsa_circ_266191,RMVar_hsa_circ_137338,RMVar_hsa_circ_370361,RMVar_hsa_circ_268055,RMVar_hsa_circ_137340,RMVar_hsa_circ_290703 101865 RMVar_ID_101865 Human_SNP_ID_37696255 m1A Human chr1 + 167424444 167424444 167424444 CCTCCCGCATAAGTCTGTACTTCCATCCCCTCATCTGTGGTAGTAGTGAAGGCTAGGTGAGTAAG CCTCCCGCATAAGTCTGTACTTCCATCCCCTCGTCTGTGGTAGTAGTGAAGGCTAGGTGAGTAAG A G POU2F1 Ensembl:ENSG00000143190 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:167424396..167424480 32194978 MeRIP-seq:(Medium) rs1159949867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331708,Human_RBP_ID_5707959,Human_RBP_ID_23342253 RMVar_hsa_circ_266191,RMVar_hsa_circ_265416 101866 RMVar_ID_101866 Human_SNP_ID_37728224 m1A Human chr1 + 167553624 167553624 167553624 TGGTAGCGGCGGCAGCCGGGAGGCCTCGTCCCAGTCCCCGTGGTCCCGGCCGCCGCGACCCCGCG TGGTAGCGGCGGCAGCCGGGAGGCCTCGTCCCCGTCCCCGTGGTCCCGGCCGCCGCGACCCCGCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:167553519..167553750 26863196 MeRIP-seq:(Medium) rs971121833 Functional Loss SNV dbSNP153 33..33 33 - - - 101867 RMVar_ID_101867 Human_SNP_ID_37728226 m1A Human chr1 - 167553626 167553626 167553626 CGCGCGGGGTCGCGGCGGCCGGGACCACGGGGACTGGGACGAGGCCTCCCGGCTGCCGCCGCTAC CGCGCGGGGTCGCGGCGGCCGGGACCACGGGGCCTGGGACGAGGCCTCCCGGCTGCCGCCGCTAC T G CREG1 Ensembl:ENSG00000143162 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:167553576..167553700 26863196 MeRIP-seq:(Medium) rs1477817306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224046,Human_RBP_ID_331819,Human_RBP_ID_972610,Human_RBP_ID_4006212,Human_RBP_ID_9319248,Human_RBP_ID_22428690,Human_RBP_ID_27171203 101868 RMVar_ID_101868 Human_SNP_ID_37767837 m1A Human chr1 + 167714780 167714780 167714780 TTCTCGCTTCGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCAGGCTTTTACCCACCC TTCTCGCTTCGGGTGCGAGAGGTCCCGGGTTCGAATCCCGGACGAGCCCAGGCTTTTACCCACCC A G tRNA-Pro-CGG-1-1 RNACentral:URS00000C18F2 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1373911061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1414967,Human_RBP_ID_5708188,Human_RBP_ID_8240289,Human_RBP_ID_8289489,Human_RBP_ID_10640062,Human_RBP_ID_17730028,Human_RBP_ID_18555341,Human_RBP_ID_19218329,Human_RBP_ID_22781018,Human_RBP_ID_23121700,Human_RBP_ID_26846141 101869 RMVar_ID_101869 Human_SNP_ID_37767850 m1A Human chr1 + 167714797 167714797 167714797 AGAGGTCCCGGGTTCAAATCCCGGACGAGCCCAGGCTTTTACCCACCCCACACCCGAAATTTAAA AGAGGTCCCGGGTTCAAATCCCGGACGAGCCCCGGCTTTTACCCACCCCACACCCGAAATTTAAA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:167714673..167714800 26863196 MeRIP-seq:(Medium) rs960671662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1439083,Human_RBP_ID_5433164,Human_RBP_ID_5708188,Human_RBP_ID_8240290,Human_RBP_ID_8289490,Human_RBP_ID_10640062,Human_RBP_ID_17730028,Human_RBP_ID_18555342,Human_RBP_ID_21998327,Human_RBP_ID_22781019,Human_RBP_ID_23121700 101870 RMVar_ID_101870 Human_SNP_ID_37767851 m1A Human chr1 + 167714797 167714797 167714797 AGAGGTCCCGGGTTCAAATCCCGGACGAGCCCAGGCTTTTACCCACCCCACACCCGAAATTTAAA AGAGGTCCCGGGTTCAAATCCCGGACGAGCCCGGGCTTTTACCCACCCCACACCCGAAATTTAAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:167714673..167714800 26863196 MeRIP-seq:(Medium) rs960671662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1439083,Human_RBP_ID_5433164,Human_RBP_ID_5708188,Human_RBP_ID_8240290,Human_RBP_ID_8289490,Human_RBP_ID_10640062,Human_RBP_ID_17730028,Human_RBP_ID_18555342,Human_RBP_ID_21998327,Human_RBP_ID_22781019,Human_RBP_ID_23121700 101871 RMVar_ID_101871 Human_SNP_ID_37767905 m1A Human chr1 + 167714887 167714887 167714887 CACATATTCCATTCAGAAACTTAAATGAAAACATACTGGTCCCATGAGCTCGAATGTTGATCCCC CACATATTCCATTCAGAAACTTAAATGAAAACGTACTGGTCCCATGAGCTCGAATGTTGATCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:167714843..167714908 26863196 MeRIP-seq:(Medium) rs900283699 Functional Loss SNV dbSNP153 33..33 33 - - - 101872 RMVar_ID_101872 Human_SNP_ID_37767906 m1A Human chr1 + 167714887 167714887 167714887 CACATATTCCATTCAGAAACTTAAATGAAAACATACTGGTCCCATGAGCTCGAATGTTGATCCCC CACATATTCCATTCAGAAACTTAAATGAAAACTTACTGGTCCCATGAGCTCGAATGTTGATCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:167714843..167714908 26863196 MeRIP-seq:(Medium) rs900283699 Functional Loss SNV dbSNP153 33..33 33 - - - 101873 RMVar_ID_101873 Human_SNP_ID_37768119 m1A Human chr1 - 167715503 167715503 167715503 TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCTGTTTTGGAGTAAGAAT TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAGATCCCGGACGAGCCCTGTTTTGGAGTAAGAAT T C lnc-ADCY10-2,TRP2,TRP-AGG1-1,lnc-ADCY10-1 RNACentral:URS00008B277F,RNACentral:URS00005DB87D,RNACentral:URS0000416117,RNACentral:URS00008B658B lincRNA,tRNA,tRNA,lincRNA intron,intron,intron,intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs1558101594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1414969,Human_RBP_ID_5456593,Human_RBP_ID_8240291,Human_RBP_ID_8289492,Human_RBP_ID_10640066,Human_RBP_ID_18205061,Human_RBP_ID_22486333,Human_RBP_ID_22781022,Human_RBP_ID_23110961,Human_RBP_ID_23121705,Human_RBP_ID_26747185 101874 RMVar_ID_101874 Human_SNP_ID_37769850 m1A Human chr1 - 167722050 167722050 167722050 GGCTTGGGGAAGAGGCTTCTGATCTCTCCGCCACCCGCGCCGGGTGGCACCTCCACGCCGCGCTC GGCTTGGGGAAGAGGCTTCTGATCTCTCCGCCCCCCGCGCCGGGTGGCACCTCCACGCCGCGCTC T G lnc-ADCY10-2,lnc-ADCY10-2:2 RNACentral:URS00008B277F,RNACentral:URS00008B44A7 lincRNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:167722001..167722175 26863196 MeRIP-seq:(Medium) rs1050808984 Functional Loss SNV dbSNP153 33..33 33 - - - 101875 RMVar_ID_101875 Human_SNP_ID_37769860 m1A Human chr1 + 167722115 167722115 167722115 GAGCCAACCTCAGCGGGGACCCGGGCTCAGGGACGCGGCGGCGGCGGCGGCGACTGCAGTGGCTG GAGCCAACCTCAGCGGGGACCCGGGCTCAGGGCCGCGGCGGCGGCGGCGGCGACTGCAGTGGCTG A C MPZL1 Ensembl:ENSG00000197965 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:167721972..167722259 26863196 MeRIP-seq:(Medium) rs961669234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331828,Human_RBP_ID_745807,Human_RBP_ID_4073138,Human_RBP_ID_5413195,Human_RBP_ID_5519249,Human_RBP_ID_9320259,Human_RBP_ID_17730029,Human_RBP_ID_18468769,Human_RBP_ID_22427693,Human_RBP_ID_23255590,Human_RBP_ID_23342350 101876 RMVar_ID_101876 Human_SNP_ID_37769872 m1A Human chr1 + 167722135 167722135 167722135 CCGGGCTCAGGGACGCGGCGGCGGCGGCGGCGACTGCAGTGGCTGGACGATGGCAGCGTCCGCCG CCGGGCTCAGGGACGCGGCGGCGGCGGCGGCGGCTGCAGTGGCTGGACGATGGCAGCGTCCGCCG A G MPZL1 Ensembl:ENSG00000197965 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:167722033..167722250 26863410 MeRIP-seq:(Medium) rs1404648805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331828,Human_RBP_ID_745807,Human_RBP_ID_4073138,Human_RBP_ID_5413195,Human_RBP_ID_5519249,Human_RBP_ID_9320259,Human_RBP_ID_17730029,Human_RBP_ID_22427693,Human_RBP_ID_23255590,Human_RBP_ID_23342350 101877 RMVar_ID_101877 Human_SNP_ID_37770506 m1A Human chr1 - 167724779 167724779 167724779 CCACATAACTCTCTAAATCTCCATTTCCAACCAGAACTTTCTCCTCACCTCCAGAACTGTCTATC CCACATAACTCTCTAAATCTCCATTTCCAACCGGAACTTTCTCCTCACCTCCAGAACTGTCTATC T C lnc-ADCY10-2,lnc-ADCY10-2:2 RNACentral:URS00008B277F,RNACentral:URS00008B44A7 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:167724777..167724880 26863196 MeRIP-seq:(Medium) rs894411336 Functional Loss SNV dbSNP153 33..33 33 - - - 101878 RMVar_ID_101878 Human_SNP_ID_37780221 m1A Human chr1 + 167765539 167765539 167765539 TTCTTGTCTGGCAAAAATGCACAGTGGTATTCATGTTAAGTCCTACTTTCAACTACCCTTATTCC TTCTTGTCTGGCAAAAATGCACAGTGGTATTCCTGTTAAGTCCTACTTTCAACTACCCTTATTCC A C MPZL1 Ensembl:ENSG00000197965 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:167765536..167765625 26863196 MeRIP-seq:(Medium) rs747579438 Functional Loss SNV dbSNP153 33..33 33 - - - 101879 RMVar_ID_101879 Human_SNP_ID_37780238 m1A Human chr1 + 167765587 167765587 167765587 TCAACTACCCTTATTCCTTTCTCTTCAGTGACAGCTGGAGTATCAGCCTTGGAAGTATATACGCC TCAACTACCCTTATTCCTTTCTCTTCAGTGACGGCTGGAGTATCAGCCTTGGAAGTATATACGCC A G MPZL1 Ensembl:ENSG00000197965 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:167765576..167765625 26863196 MeRIP-seq:(Medium) rs763026238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331830,Human_RBP_ID_803193,Human_RBP_ID_853048,Human_RBP_ID_4073140 Human_Splice_Rec_154458,Human_Splice_Rec_154460,Human_Splice_Rec_154470,Human_Splice_Rec_154478,Human_Splice_Rec_154482,Human_Splice_Rec_154488 RMVar_hsa_circ_137353,RMVar_hsa_circ_269973,RMVar_hsa_circ_323389,RMVar_hsa_circ_332391,RMVar_hsa_circ_377373,RMVar_hsa_circ_293976,RMVar_hsa_circ_137354,RMVar_hsa_circ_137351,RMVar_hsa_circ_137352,RMVar_hsa_circ_137350 101880 RMVar_ID_101880 Human_SNP_ID_37785797 m1A Human chr1 + 167789547 167789547 167789547 TAAAACAGGATTGAGATTTTGAGGTGTGCACAAGGTGGTAAGATAAAGGGCATATGAGCTTCAAA TAAAACAGGATTGAGATTTTGAGGTGTGCACAGGGTGGTAAGATAAAGGGCATATGAGCTTCAAA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs3752606 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13389,GWAS_ID_13390,GWAS_ID_13391,GWAS_ID_13392,GWAS_ID_13393,GWAS_ID_13394,GWAS_ID_13395,GWAS_ID_13396 101881 RMVar_ID_101881 Human_SNP_ID_37821807 m1A Human chr1 + 167935850 167935835 167935850 GCCTCGGGCACCGGCGGCCGACATCGCCGCCGAGGGATCGTTGGCAGCCGGGTGGGAGCGTGGCT GCCTCGGGCACCGGCGGC_______________GGGATCGTTGGCAGCCGGGTGGGAGCGTGGCT CCGACATCGCCGCCGA C DCAF6 Ensembl:ENSG00000143164 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:167935826..167935850 26863196 MeRIP-seq:(Medium) rs545944343 Functional Loss DEL dbSNP153 19..33 33 - - - 101882 RMVar_ID_101882 Human_SNP_ID_37821826 m1A Human chr1 + 167935874 167935874 167935874 CGCCGCCGAGGGATCGTTGGCAGCCGGGTGGGAGCGTGGCTGTGTTCTCGTCCCTGGCTGACAAC CGCCGCCGAGGGATCGTTGGCAGCCGGGTGGGGGCGTGGCTGTGTTCTCGTCCCTGGCTGACAAC A G DCAF6 Ensembl:ENSG00000143164 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:167935826..167935932 26863196 MeRIP-seq:(Medium) rs1183214154 Functional Loss SNV dbSNP153 33..33 33 - - - 101883 RMVar_ID_101883 Human_SNP_ID_37869762 m1A Human chr1 - 168131311 168131311 168131311 GTAGAGGGTATTTGCAAATGAATAAATTCTGCAGGTGGCAGGGAATAGCATGAAATGGTCTGGCT GTAGAGGGTATTTGCAAATGAATAAATTCTGCTGGTGGCAGGGAATAGCATGAAATGGTCTGGCT T A GPR161 Ensembl:ENSG00000143147 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:168131301..168131444 26863196 MeRIP-seq:(Medium) rs1436041681 Functional Loss SNV dbSNP153 33..33 33 - - - 101884 RMVar_ID_101884 Human_SNP_ID_37871096 m1A Human chr1 - 168136812 168136812 168136812 CCTCCAGTCCCGGAGCGCGGCGGGGAGGAAGGAAGCGGCGGCGGCGGTGGCCGAGGCGGGGAGGC CCTCCAGTCCCGGAGCGCGGCGGGGAGGAAGGGAGCGGCGGCGGCGGTGGCCGAGGCGGGGAGGC T C GPR161 Ensembl:ENSG00000143147 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:168136687..168137029 26863196 MeRIP-seq:(Medium) rs1326856434 Functional Loss SNV dbSNP153 33..33 33 - - - 101885 RMVar_ID_101885 Human_SNP_ID_37881428 m1A Human chr1 - 168178963 168178963 168178963 GGCCCAGCCTCCTAGGCTTCCGAGCCGTTACCATGCCCGGCCCCGCCCCCTGCCGGCCGACCCGG GGCCCAGCCTCCTAGGCTTCCGAGCCGTTACCGTGCCCGGCCCCGCCCCCTGCCGGCCGACCCGG T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:168178917..168179004 26863410 MeRIP-seq:(Medium) rs1284157554 Functional Loss SNV dbSNP153 33..33 33 - - - 101886 RMVar_ID_101886 Human_SNP_ID_37881479 m1A Human chr1 - 168179057 168179057 168179057 GTGGATCATCATGGCTGAGGCAGGACCCGCAGAGGCCACAAGGAATAAGCTGAAGCAGCGGCGGC GTGGATCATCATGGCTGAGGCAGGACCCGCAGGGGCCACAAGGAATAAGCTGAAGCAGCGGCGGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:168178956..168179056 26863410 MeRIP-seq:(Medium) rs375198968 Functional Loss SNV dbSNP153 33..33 33 - - - 101887 RMVar_ID_101887 Human_SNP_ID_37881790 m1A Human chr1 - 168180272 168180272 168180272 AAAGGCATACGATACATGCAAAAATCCAAGCCAGAGATCTTGTCATCAGCATAGACTCTTCCTTT AAAGGCATACGATACATGCAAAAATCCAAGCCGGAGATCTTGTCATCAGCATAGACTCTTCCTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:168180270..168180414;chr1:168180271..168180427 26863196 MeRIP-seq:(Medium) rs968822574 Functional Loss SNV dbSNP153 33..33 33 - - - 101888 RMVar_ID_101888 Human_SNP_ID_37893494 m1A Human chr1 - 168226081 168226081 168226081 CCTGCCCGCTCAGCACCTTCTTCAGCTTGTCCATTGCGGCCCAGTCCCCACCAGCTCCAGCTCCT CCTGCCCGCTCAGCACCTTCTTCAGCTTGTCCCTTGCGGCCCAGTCCCCACCAGCTCCAGCTCCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:168226032..168226199 26863196 MeRIP-seq:(Medium) rs1158746138 Functional Loss SNV dbSNP153 33..33 33 - - - 101889 RMVar_ID_101889 Human_SNP_ID_38111074 m1A Human chr1 - 169106643 169106643 169106643 GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGAGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGGGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:169106326..169106802 26863196 MeRIP-seq:(Medium) rs1464228568 Functional Loss SNV dbSNP153 33..33 33 - - - 101890 RMVar_ID_101890 Human_SNP_ID_38111075 m1A Human chr1 - 169106643 169106643 169106643 GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGAGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:169106326..169106802 26863196 MeRIP-seq:(Medium) rs1464228568 Functional Loss SNV dbSNP153 33..33 33 - - - 101891 RMVar_ID_101891 Human_SNP_ID_38112530 m1A Human chr1 + 169111461 169111461 169111461 ACCATCCAAGTGATGCTGCTCACCATCAGTGAATTTAAGCCCACATATCAGGACCGAGTGGCCCC ACCATCCAAGTGATGCTGCTCACCATCAGTGACTTTAAGCCCACATATCAGGACCGAGTGGCCCC A C ATP1B1 Ensembl:ENSG00000143153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:169111329..169111540 26863196 MeRIP-seq:(Medium) rs557213061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332441,Human_RBP_ID_22429859 Human_Splice_Rec_155326,Human_Splice_Rec_155327,Human_Splice_Rec_155334,Human_Splice_Rec_155335,Human_Splice_Rec_155342,Human_Splice_Rec_155343 Human_miRNA_ID_455232,Human_miRNA_ID_457185,Human_miRNA_ID_732169,Human_miRNA_ID_2147746,Human_miRNA_ID_2148545,Human_miRNA_ID_2296769 RMVar_hsa_circ_137426,RMVar_hsa_circ_82070,RMVar_hsa_circ_137425,RMVar_hsa_circ_68623 101892 RMVar_ID_101892 Human_SNP_ID_38112531 m1A Human chr1 + 169111461 169111461 169111461 ACCATCCAAGTGATGCTGCTCACCATCAGTGAATTTAAGCCCACATATCAGGACCGAGTGGCCCC ACCATCCAAGTGATGCTGCTCACCATCAGTGAGTTTAAGCCCACATATCAGGACCGAGTGGCCCC A G ATP1B1 Ensembl:ENSG00000143153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:169111329..169111540 26863196 MeRIP-seq:(Medium) rs557213061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332441,Human_RBP_ID_22429859 Human_Splice_Rec_155326,Human_Splice_Rec_155327,Human_Splice_Rec_155334,Human_Splice_Rec_155335,Human_Splice_Rec_155342,Human_Splice_Rec_155343 Human_miRNA_ID_455232,Human_miRNA_ID_457185,Human_miRNA_ID_732169,Human_miRNA_ID_2147746,Human_miRNA_ID_2148545,Human_miRNA_ID_2296769 RMVar_hsa_circ_137426,RMVar_hsa_circ_82070,RMVar_hsa_circ_137425,RMVar_hsa_circ_68623 101893 RMVar_ID_101893 Human_SNP_ID_38171014 m1A Human chr1 - 169360640 169360640 169360640 CAGGTGAAACCTAGGAGAAGAGCATTCCAGGCAGAGTCAATAGTGAGCACAGAGGTGCATTAGAG CAGGTGAAACCTAGGAGAAGAGCATTCCAGGCGGAGTCAATAGTGAGCACAGAGGTGCATTAGAG T C NME7 Ensembl:ENSG00000143156 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:169360575..169360680 26863196 MeRIP-seq:(Medium) rs147598745 Functional Loss SNV dbSNP153 33..33 33 - - - 101894 RMVar_ID_101894 Human_SNP_ID_38275075 m1A Human chr1 - 169794871 169794871 169794871 GTGCGCGATTTAGGTCCGGAGGAGGCGTTGTGAGGTGAGCTTTTTCAGAAGCGCGATCCCAGGAC GTGCGCGATTTAGGTCCGGAGGAGGCGTTGTGTGGTGAGCTTTTTCAGAAGCGCGATCCCAGGAC T A METTL18 Ensembl:ENSG00000171806 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:169794791..169794874 26863196 MeRIP-seq:(Medium) rs1384053592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_156341,Human_Splice_Rec_156343 101895 RMVar_ID_101895 Human_SNP_ID_38275171 m1A Human chr1 + 169795113 169795113 169795113 AGCTCTCCTGTTTGACGAAAGTATGTCTCAGGAAGGTGCGGTCCCAGCTAGCGCGGTTCCCCTGG AGCTCTCCTGTTTGACGAAAGTATGTCTCAGGGAGGTGCGGTCCCAGCTAGCGCGGTTCCCCTGG A G C1orf112 Ensembl:ENSG00000000460 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:169794814..169795170 26863196 MeRIP-seq:(Medium) rs1248940080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4084754,Human_RBP_ID_18415096,Human_RBP_ID_18555777,Human_RBP_ID_22781090,Human_RBP_ID_22849937,Human_RBP_ID_23343941 Human_Splice_Rec_155957 RMVar_hsa_circ_128099,RMVar_hsa_circ_137457 101896 RMVar_ID_101896 Human_SNP_ID_38292878 m1A Human chr1 + 169865580 169865580 169865580 CTTCTGCTAGCTCCTTTCCCTCGTCTATTAATATGCTCAGGTCTCTTCCACCCTTACAAAATCCT CTTCTGCTAGCTCCTTTCCCTCGTCTATTAATGTGCTCAGGTCTCTTCCACCCTTACAAAATCCT A G NONHSAG003421.2,NONHSAG003421.2:2 RNACentral:URS00008BA77C,RNACentral:URS00008BEB0C lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:169865529..169865727 26863196 MeRIP-seq:(Medium) rs1558125827 Functional Loss SNV dbSNP153 33..33 33 - - - 101897 RMVar_ID_101897 Human_SNP_ID_38292938 m1A Human chr1 - 169865844 169865840 169865844 TGAATGAGAAGCAGGGGTTAGAGGAGACTCAGAGAGCTAGGAAGGCTATGATATTCCCAAAGGAG TGAATGAGAAGCAGGGGTTAGAGGAGACTCAG____CTAGGAAGGCTATGATATTCCCAAAGGAG GCTCT G SCYL3 Ensembl:ENSG00000000457 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:169865822..169865887 26863196 MeRIP-seq:(Medium) rs1036049232 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_137477,RMVar_hsa_circ_66265,RMVar_hsa_circ_74023,RMVar_hsa_circ_323557,RMVar_hsa_circ_338773,RMVar_hsa_circ_354094,RMVar_hsa_circ_326778,RMVar_hsa_circ_56680,RMVar_hsa_circ_373506,RMVar_hsa_circ_137479 101898 RMVar_ID_101898 Human_SNP_ID_38449466 m1A Human chr1 - 170532199 170532199 170532199 TGCGCCATCGGCCCGGGCCACCGGCACCCCCAAAAGTGCCCAAATCTCGCAGCCGCGACTGCCAA TGCGCCATCGGCCCGGGCCACCGGCACCCCCAGAAGTGCCCAAATCTCGCAGCCGCGACTGCCAA T C GORAB-AS1 Ensembl:ENSG00000231407 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:170532154..170532558 26863196 MeRIP-seq:(Medium) rs769657515 Functional Loss SNV dbSNP153 33..33 33 - - - 101899 RMVar_ID_101899 Human_SNP_ID_38449473 m1A Human chr1 - 170532206 170532206 170532206 CCAACCTTGCGCCATCGGCCCGGGCCACCGGCACCCCCAAAAGTGCCCAAATCTCGCAGCCGCGA CCAACCTTGCGCCATCGGCCCGGGCCACCGGCGCCCCCAAAAGTGCCCAAATCTCGCAGCCGCGA T C GORAB-AS1 Ensembl:ENSG00000231407 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:170532160..170533507 26863196 MeRIP-seq:(Medium) rs1291165772 Functional Loss SNV dbSNP153 33..33 33 - - - 101900 RMVar_ID_101900 Human_SNP_ID_38684659 m1A Human chr1 - 171485596 171485596 171485596 CAGACTGGAAAAGCCGAAGCTGCGGATGGACAAACCGCCAAAGCACTTTCGCAGCTTTCCGAGGG CAGACTGGAAAAGCCGAAGCTGCGGATGGACAGACCGCCAAAGCACTTTCGCAGCTTTCCGAGGG T C lnc-MYOC-7 RNACentral:URS0000D5AD06 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:171485551..171485750 26863196 MeRIP-seq:(Medium) rs368146439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5254286,Human_RBP_ID_5414490,Human_RBP_ID_5433193,Human_RBP_ID_5712020,Human_RBP_ID_16970765,Human_RBP_ID_17675679,Human_RBP_ID_17730788,Human_RBP_ID_23260652 101901 RMVar_ID_101901 Human_SNP_ID_38684660 m1A Human chr1 + 171485602 171485602 171485602 GAAAGCTGCGAAAGTGCTTTGGCGGTTTGTCCATCCGCAGCTTCGGCTTTTCCAGTCTGGTGGCC GAAAGCTGCGAAAGTGCTTTGGCGGTTTGTCCGTCCGCAGCTTCGGCTTTTCCAGTCTGGTGGCC A G PRRC2C Ensembl:ENSG00000117523 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:171485551..171485703;chr1:171485551..171485750 26863196 MeRIP-seq:(Medium) rs1188406777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25985,Human_RBP_ID_4007672,Human_RBP_ID_8290161,Human_RBP_ID_9357113,Human_RBP_ID_18555893,Human_RBP_ID_23344264,Human_RBP_ID_26312141,Human_RBP_ID_26846723,Human_RBP_ID_27171528 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 101902 RMVar_ID_101902 Human_SNP_ID_38696633 m1A Human chr1 - 171532650 171532638 171532650 CCTTCTCTCGCTCCTGTTCTTGTTCTTTTTCAAGTTCTTTCTCACGCTCCCGTTCTTTTTCTCGC CCTTCTCTCGCTCCTGTTCTTGTTCTTTTTCA____________CGCTCCCGTTCTTTTTCTCGC GTGAGAAAGAACT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:171532600..171532975 26863196 MeRIP-seq:(Medium) rs1557932852 Functional Loss DEL dbSNP153 33..44 33 - - - 101903 RMVar_ID_101903 Human_SNP_ID_38696667 m1A Human chr1 + 171532757 171532757 171532757 AGCTGGAGAAGGAGCAGGAAAAACAAAGAGAAATGGAGAAAGAAAGAAAGCAAGAAAAAGAAAAA AGCTGGAGAAGGAGCAGGAAAAACAAAGAGAATTGGAGAAAGAAAGAAAGCAAGAAAAAGAAAAA A T PRRC2C Ensembl:ENSG00000117523 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:171532435..171532975;chr1:171532461..171532975;chr1:171532426..171532975 26863196 MeRIP-seq:(Medium) rs1224432988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1438218,Human_RBP_ID_2103935,Human_RBP_ID_8290230,Human_RBP_ID_17447529,Human_RBP_ID_17646594,Human_RBP_ID_22850038,Human_RBP_ID_23344531,Human_RBP_ID_24541533 Human_miRNA_ID_264022,Human_miRNA_ID_1538547,Human_miRNA_ID_1592825,Human_miRNA_ID_2046450 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_97212,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_137543 101904 RMVar_ID_101904 Human_SNP_ID_38696682 m1A Human chr1 + 171532789 171532787 171532790 ATGGAGAAAGAAAGAAAGCAAGAAAAAGAAAAAGAACTAGAACGGCAGAAAGAAAAGGAAAAAGA ATGGAGAAAGAAAGAAAGCAAGAAAAAGAAA___AACTAGAACGGCAGAAAGAAAAGGAAAAAGA AAAG A PRRC2C Ensembl:ENSG00000117523 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:171532453..171532975 26863196 MeRIP-seq:(Medium) rs778918654 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1438219,Human_RBP_ID_2103936,Human_RBP_ID_5544800,Human_RBP_ID_17646594,Human_RBP_ID_22850040 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_97212,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_137543 101905 RMVar_ID_101905 Human_SNP_ID_38697269 m1A Human chr1 - 171535329 171535329 171535329 CAAAGACTGAGGTATAATAAAAGTTAATGAGGAAGAAAATATCCTCGACACTCTAAAACATTATT CAAAGACTGAGGTATAATAAAAGTTAATGAGGGAGAAAATATCCTCGACACTCTAAAACATTATT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:171535312..171535550 26863196 MeRIP-seq:(Medium) rs930182302 Functional Loss SNV dbSNP153 33..33 33 - - - 101906 RMVar_ID_101906 Human_SNP_ID_38697279 m1A Human chr1 - 171535373 171535373 171535373 GTAATAGTATTCATCTATGACACTTATCAAACACAGGATTTTTACAAAGACTGAGGTATAATAAA GTAATAGTATTCATCTATGACACTTATCAAACGCAGGATTTTTACAAAGACTGAGGTATAATAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:171535370..171535525 26863196 MeRIP-seq:(Medium) rs1283149911 Functional Loss SNV dbSNP153 33..33 33 - - - 101907 RMVar_ID_101907 Human_SNP_ID_38697321 m1A Human chr1 + 171535466 171535466 171535466 AACCCGTTTTCACTAGACAAGACAGCAATCGCAGTGAAAAGGAAGCCACACCAGTGGTGCATGAA AACCCGTTTTCACTAGACAAGACAGCAATCGCCGTGAAAAGGAAGCCACACCAGTGGTGCATGAA A C PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:171535426..171535525 26863196 MeRIP-seq:(Medium) rs754082014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18742,Human_RBP_ID_1415422,Human_RBP_ID_9357140,Human_RBP_ID_18555975,Human_RBP_ID_24747020,Human_RBP_ID_26309849,Human_RBP_ID_26846805 Human_Splice_Rec_157282,Human_Splice_Rec_157348,Human_Splice_Rec_157424 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_137540,RMVar_hsa_circ_97212,RMVar_hsa_circ_356800,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_373034,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_364102,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_318239,RMVar_hsa_circ_319804,RMVar_hsa_circ_280025,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_137546 101908 RMVar_ID_101908 Human_SNP_ID_38697349 m1A Human chr1 + 171535548 171535548 171535548 GTCTCAACCTCGGCCGGCTGTATTATCTGGCTATTTCAAACAGTTTCAGAAGTCTTTACCTCCAC GTCTCAACCTCGGCCGGCTGTATTATCTGGCTGTTTCAAACAGTTTCAGAAGTCTTTACCTCCAC A G PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:171535372..171535600 26863196 MeRIP-seq:(Medium) rs1414744292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1729099,Human_RBP_ID_8737849,Human_RBP_ID_9359583,Human_RBP_ID_17213725,Human_RBP_ID_17331423,Human_RBP_ID_26846806 Human_Splice_Rec_157283,Human_Splice_Rec_157349,Human_Splice_Rec_157425 Human_miRNA_ID_2646686,Human_miRNA_ID_2669279,Human_miRNA_ID_3099927 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_137540,RMVar_hsa_circ_97212,RMVar_hsa_circ_356800,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_373034,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_364102,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_318239,RMVar_hsa_circ_319804,RMVar_hsa_circ_280025,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_137546 101909 RMVar_ID_101909 Human_SNP_ID_38697350 m1A Human chr1 + 171535548 171535548 171535548 GTCTCAACCTCGGCCGGCTGTATTATCTGGCTATTTCAAACAGTTTCAGAAGTCTTTACCTCCAC GTCTCAACCTCGGCCGGCTGTATTATCTGGCTTTTTCAAACAGTTTCAGAAGTCTTTACCTCCAC A T PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:171535372..171535600 26863196 MeRIP-seq:(Medium) rs1414744292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1729099,Human_RBP_ID_8737849,Human_RBP_ID_9359583,Human_RBP_ID_17213725,Human_RBP_ID_17331423,Human_RBP_ID_26846806 Human_Splice_Rec_157283,Human_Splice_Rec_157349,Human_Splice_Rec_157425 Human_miRNA_ID_2646686,Human_miRNA_ID_2669279,Human_miRNA_ID_3099927 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_137540,RMVar_hsa_circ_97212,RMVar_hsa_circ_356800,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_373034,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_364102,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_318239,RMVar_hsa_circ_319804,RMVar_hsa_circ_280025,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_137546 101910 RMVar_ID_101910 Human_SNP_ID_38703204 m1A Human chr1 - 171557427 171557427 171557427 TTGAGGCTGGAACTGGAGTTAAGGTTGCCGGAAGTGGAGCTGAGGTTGAGGCTGGAACTGAAGCT TTGAGGCTGGAACTGGAGTTAAGGTTGCCGGAGGTGGAGCTGAGGTTGAGGCTGGAACTGAAGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:171557376..171557922 26863196 MeRIP-seq:(Medium) rs946660586 Functional Loss SNV dbSNP153 33..33 33 - - - 101911 RMVar_ID_101911 Human_SNP_ID_38703232 m1A Human chr1 - 171557472 171557472 171557472 AGGCCAGAACTGGAGCTAAAGTTGAGGCTGGAACCGGAGCTGAGGTTGAGGCTGGAACTGGAGTT AGGCCAGAACTGGAGCTAAAGTTGAGGCTGGAGCCGGAGCTGAGGTTGAGGCTGGAACTGGAGTT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:171557376..171557925 26863196 MeRIP-seq:(Medium) rs1316250141 Functional Loss SNV dbSNP153 33..33 33 - - - 101912 RMVar_ID_101912 Human_SNP_ID_38703281 m1A Human chr1 - 171557562 171557562 171557562 CAGCTGAAGTAGAGGCTGGAACTGAAGCTGAGACTGAGGCTGAGGCTGAAACTGGAGCTAAGGGT CAGCTGAAGTAGAGGCTGGAACTGAAGCTGAGGCTGAGGCTGAGGCTGAAACTGGAGCTAAGGGT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:171557461..171557993 26863410 MeRIP-seq:(Medium) rs1557997473 Functional Loss SNV dbSNP153 33..33 33 - - - 101913 RMVar_ID_101913 Human_SNP_ID_38703295 m1A Human chr1 - 171557601 171557601 171557601 CTGGGGCTGAGGCTGGAGCTGAAGAAGAGGTTATAGCTGCAGCTGAAGTAGAGGCTGGAACTGAA CTGGGGCTGAGGCTGGAGCTGAAGAAGAGGTTGTAGCTGCAGCTGAAGTAGAGGCTGGAACTGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:171557551..171557875 26863196 MeRIP-seq:(Medium) rs1179471794 Functional Loss SNV dbSNP153 33..33 33 - - - 101914 RMVar_ID_101914 Human_SNP_ID_38703426 m1A Human chr1 + 171557922 171557922 171557922 TGCCCCACCTGCCCCAGCCCAGACTCAGGCACAGACCCACAAACCAGTCCAGAATCCACTACAGA TGCCCCACCTGCCCCAGCCCAGACTCAGGCACTGACCCACAAACCAGTCCAGAATCCACTACAGA A T PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:171557876..171558025 26863196 MeRIP-seq:(Medium) rs765562372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221577,Human_RBP_ID_2104068,Human_RBP_ID_5125315,Human_RBP_ID_17071260,Human_RBP_ID_17331440,Human_RBP_ID_17456340,Human_RBP_ID_17647808,Human_RBP_ID_18928779,Human_RBP_ID_22751387 Human_miRNA_ID_473303,Human_miRNA_ID_1979907,Human_miRNA_ID_1981631,Human_miRNA_ID_2541075,Human_miRNA_ID_2544825,Human_miRNA_ID_2557682,Human_miRNA_ID_2588096 RMVar_hsa_circ_34691,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_96232,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_97212,RMVar_hsa_circ_137544,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_319804,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_32414,RMVar_hsa_circ_85082,RMVar_hsa_circ_120034,RMVar_hsa_circ_137551,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_333326,RMVar_hsa_circ_137554 101915 RMVar_ID_101915 Human_SNP_ID_38731236 m1A Human chr1 - 171670653 171670653 171670653 CATGGATCTTCGTATACCAAGAGTACCGGTGGAGCCCCCACCTTCAATGTCACTGTCACCAAGAC CATGGATCTTCGTATACCAAGAGTACCGGTGGGGCCCCCACCTTCAATGTCACTGTCACCAAGAC T C PFN1P1 Ensembl:ENSG00000233328 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879022697 Functional Loss SNV dbSNP153 33..33 33 - - - 101916 RMVar_ID_101916 Human_SNP_ID_38748346 m1A Human chr1 - 171741563 171741563 171741563 ATTCCAGGGGGTACAATGGGGCAGGAAGGGCCAGCGTTAGGAGCAGATATATCGTGGGACGTGGC ATTCCAGGGGGTACAATGGGGCAGGAAGGGCCGGCGTTAGGAGCAGATATATCGTGGGACGTGGC T C VAMP4 Ensembl:ENSG00000117533 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:171741512..171741641 26863196 MeRIP-seq:(Medium) rs529947882 Functional Loss SNV dbSNP153 33..33 33 - - - 101917 RMVar_ID_101917 Human_SNP_ID_38748348 m1A Human chr1 - 171741581 171741581 171741581 AGTGGGATGTAGTGAGGAATTCCAGGGGGTACAATGGGGCAGGAAGGGCCAGCGTTAGGAGCAGA AGTGGGATGTAGTGAGGAATTCCAGGGGGTACGATGGGGCAGGAAGGGCCAGCGTTAGGAGCAGA T C VAMP4 Ensembl:ENSG00000117533 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:171741569..171741806 26863196 MeRIP-seq:(Medium) rs1558118022 Functional Loss SNV dbSNP153 33..33 33 - - - 101918 RMVar_ID_101918 Human_SNP_ID_38757584 m1A Human chr1 + 171781730 171781730 171781730 AAAAGTGTGAGGGGCTCTTCACGTGGGGAAGGAACAGCAGGCGCGGAGGAGGGGGCAAGCGTGTG AAAAGTGTGAGGGGCTCTTCACGTGGGGAAGGGACAGCAGGCGCGGAGGAGGGGGCAAGCGTGTG A G EEF1AKNMT Ensembl:ENSG00000010165 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:171781649..171781898;chr1:171781647..171782079;chr1:171781648..171783900;chr1:171781660..171781950 26863196 MeRIP-seq:(Medium) rs776454438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16797,Human_RBP_ID_741310,Human_RBP_ID_800801,Human_RBP_ID_4008097,Human_RBP_ID_5086129,Human_RBP_ID_5136901,Human_RBP_ID_9320270,Human_RBP_ID_18415098 Human_Splice_Rec_157687,Human_Splice_Rec_157693 RMVar_hsa_circ_87704,RMVar_hsa_circ_137587 101919 RMVar_ID_101919 Human_SNP_ID_38758432 m1A Human chr1 - 171784380 171784380 171784380 CCCCATCGCACAAGTCCAGAGACACACTCCCCAGCCTGGCCTTGCGGCGCAGCTGGCTGCACAGC CCCCATCGCACAAGTCCAGAGACACACTCCCCCGCCTGGCCTTGCGGCGCAGCTGGCTGCACAGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:171783978..171784426 32194978 MeRIP-seq:(Medium) rs878939583 Functional Loss SNV dbSNP153 33..33 33 - - - 101920 RMVar_ID_101920 Human_SNP_ID_38772036 m1A Human chr1 + 171841679 171841679 171841679 CTCGGGCAAGATGGGGAACCGGGAGATGGAGGAGCTGATCCCGCTGGTGAACCGTCTGCAGGACG CTCGGGCAAGATGGGGAACCGGGAGATGGAGGGGCTGATCCCGCTGGTGAACCGTCTGCAGGACG A G DNM3 Ensembl:ENSG00000197959 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:171841529..171841692 26863196 MeRIP-seq:(Medium) rs1313104093 Functional Loss SNV dbSNP153 33..33 33 - - - 101921 RMVar_ID_101921 Human_SNP_ID_38908063 m1A Human chr1 + 172441890 172441890 172441890 GGCAAAGAGTACGGCTCCCACAGCACTAATGGACAGTAGGCCTCCCACGGCTGAAAATGCAAAAA GGCAAAGAGTACGGCTCCCACAGCACTAATGGGCAGTAGGCCTCCCACGGCTGAAAATGCAAAAA A G C1orf105 Ensembl:ENSG00000180999 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:172441803..172442102 32194978 MeRIP-seq:(Medium) rs559302185 Functional Loss SNV dbSNP153 33..33 33 - - - 101922 RMVar_ID_101922 Human_SNP_ID_38929113 m1A Human chr1 + 172533187 172533187 172533187 GCGGCAGTGGCGGCTGCAGGAGGCGGGCGTGGACGAGCCGGTGGCTGCAGCGGCGGCGGTCCCCG GCGGCAGTGGCGGCTGCAGGAGGCGGGCGTGGGCGAGCCGGTGGCTGCAGCGGCGGCGGTCCCCG A G SUCO Ensembl:ENSG00000094975 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:172532798..172533316 26863196 MeRIP-seq:(Medium) rs1386106627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073161,Human_RBP_ID_22429869,Human_RBP_ID_22870993,Human_RBP_ID_26773188 101923 RMVar_ID_101923 Human_SNP_ID_38929122 m1A Human chr1 - 172533196 172533196 172533196 ACAGGACTCCGGGGACCGCCGCCGCTGCAGCCACCGGCTCGTCCACGCCCGCCTCCTGCAGCCGC ACAGGACTCCGGGGACCGCCGCCGCTGCAGCCTCCGGCTCGTCCACGCCCGCCTCCTGCAGCCGC T A lnc-PIGC-4 RNACentral:URS00009BD11B lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:172533043..172533316 26863196 MeRIP-seq:(Medium) rs1263415642 Functional Loss SNV dbSNP153 33..33 33 - - - 101924 RMVar_ID_101924 Human_SNP_ID_39139201 m1A Human chr1 - 173441271 173441271 173441271 AGAAACTAGGAAAAGCAAAGAGAAGGGAGGGGAAAAAGGATGAAAAAGAAGAAAAGGGTGAGAAG AGAAACTAGGAAAAGCAAAGAGAAGGGAGGGGGAAAAGGATGAAAAAGAAGAAAAGGGTGAGAAG T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:173441131..173441376 26863196 MeRIP-seq:(Medium) rs1047888431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308527,RMVar_hsa_circ_137630 101925 RMVar_ID_101925 Human_SNP_ID_39139879 m1A Human chr1 - 173444119 173444119 173444119 AAATAAATGGTTTCGATTTTGGTATTTGGACAAGGCTTGAAGTGGAATCTCCTGGTGAACAAAAT AAATAAATGGTTTCGATTTTGGTATTTGGACAGGGCTTGAAGTGGAATCTCCTGGTGAACAAAAT T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:173444081..173444268 26863196 MeRIP-seq:(Medium) rs925925188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2104690,Human_RBP_ID_5540463,Human_RBP_ID_23345423 101926 RMVar_ID_101926 Human_SNP_ID_39147607 m1A Human chr1 + 173477452 173477452 173477452 GGGACGTGGCTCCCAACTTTGAGGCCAATACCACCGTCGGCCGCATCCGTTTCCACGACTTTCTG GGGACGTGGCTCCCAACTTTGAGGCCAATACCTCCGTCGGCCGCATCCGTTTCCACGACTTTCTG A T PRDX6 Ensembl:ENSG00000117592 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr1:173477301..173477555;chr1:173477351..173477573 26863196 MeRIP-seq:(Medium) rs1280994761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221588,Human_RBP_ID_742276,Human_RBP_ID_4008655,Human_RBP_ID_8290601,Human_RBP_ID_17338568,Human_RBP_ID_18187332,Human_RBP_ID_22026090,Human_RBP_ID_22429870,Human_RBP_ID_22532173,Human_RBP_ID_26799187,Human_RBP_ID_27391193 Human_Splice_Rec_158337,Human_Splice_Rec_158339 RMVar_hsa_circ_110680,RMVar_hsa_circ_137631 101927 RMVar_ID_101927 Human_SNP_ID_39148425 m1A Human chr1 + 173481229 173481229 173481229 TAAATATCATCATAAGCATTCATTTAAAAAAGAAAGCCTGTTTTTGATCCAGAAGTTGTGACTTT TAAATATCATCATAAGCATTCATTTAAAAAAGCAAGCCTGTTTTTGATCCAGAAGTTGTGACTTT A C PRDX6 Ensembl:ENSG00000117592 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:173481227..173481358 26863196 MeRIP-seq:(Medium) rs969166016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10656089,Human_RBP_ID_23345467 RMVar_hsa_circ_110680,RMVar_hsa_circ_137631 101928 RMVar_ID_101928 Human_SNP_ID_39149875 m1A Human chr1 + 173487163 173487163 173487163 TTATTAAGTGGTGATAACAGGTGCTACAGGGAAGAATCAAGCACAGATGGGGAGAATAACAGCAC TTATTAAGTGGTGATAACAGGTGCTACAGGGACGAATCAAGCACAGATGGGGAGAATAACAGCAC A C PRDX6 Ensembl:ENSG00000117592 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:173487160..173487380 26863196 MeRIP-seq:(Medium) rs773312002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18556364 RMVar_hsa_circ_82049,RMVar_hsa_circ_110680,RMVar_hsa_circ_137631,RMVar_hsa_circ_103400,RMVar_hsa_circ_137632,RMVar_hsa_circ_99726,RMVar_hsa_circ_137634,RMVar_hsa_circ_137635 101929 RMVar_ID_101929 Human_SNP_ID_39150224 m1A Human chr1 - 173488601 173488601 173488601 TGTGTGAAAGGCACATGGCACTAATATTGCTCACACCTGCTACACCTCCTTGGGAGCCAAGGGAA TGTGTGAAAGGCACATGGCACTAATATTGCTCTCACCTGCTACACCTCCTTGGGAGCCAAGGGAA T A AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:173488510..173488610 32194978 MeRIP-seq:(Medium) rs774813022 Functional Loss SNV dbSNP153 33..33 33 - - - 101930 RMVar_ID_101930 Human_SNP_ID_39194934 m1A Human chr1 - 173688609 173688605 173688609 AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAGAGAGGAAGAGGCAGAGAGAGAGAGAGGAAGCGG AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAG____GAAGAGGCAGAGAGAGAGAGAGGAAGCGG CCTCT C lnc-ANKRD45-3 RNACentral:URS0000D57E23 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:173688559..173688642 26863196 MeRIP-seq:(Medium) rs771296140 Functional Loss DEL dbSNP153 33..36 33 - - - 101931 RMVar_ID_101931 Human_SNP_ID_39194935 m1A Human chr1 - 173688609 173688605 173688609 AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAGAGAGGAAGAGGCAGAGAGAGAGAGAGGAAGCGG AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAG__AGGAAGAGGCAGAGAGAGAGAGAGGAAGCGG CCTCT CCT lnc-ANKRD45-3 RNACentral:URS0000D57E23 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:173688559..173688642 26863196 MeRIP-seq:(Medium) rs771296140 Functional Loss DEL dbSNP153 33..34 33 - - - 101932 RMVar_ID_101932 Human_SNP_ID_39225324 m1A Human chr1 + 173822274 173822274 173822274 ATGGCCAAATACTTTGTTCATCAAGTTTGTTCATCCTTACTCCTCTAAACTTTCTGGGACCTTGT ATGGCCAAATACTTTGTTCATCAAGTTTGTTCGTCCTTACTCCTCTAAACTTTCTGGGACCTTGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:173822224..173822417 26863196 MeRIP-seq:(Medium) rs78676378 Functional Loss SNV dbSNP153 33..33 33 - - - 101933 RMVar_ID_101933 Human_SNP_ID_39236478 m1A Human chr1 + 173865478 173865473 173865479 ACGTTAACATCAATAAAACATGTACCTTTAAAAGGTATGACAGGAACTGTCTTCATGTCCTTACC ACGTTAACATCAATAAAACATGTACCTT______GTATGACAGGAACTGTCTTCATGTCCTTACC TTAAAAG T lnc-ZBTB37-2 RNACentral:URS00008B82B3 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:173865476..173865525 32194978 MeRIP-seq:(Medium) rs1417771847 Functional Loss DEL dbSNP153 29..34 33 - - - 101934 RMVar_ID_101934 Human_SNP_ID_39237515 m1A Human chr1 + 173867898 173867898 173867898 ACTGGCTTAGAAGTCCCAGTCAATTCAGGGTGACCTTAGCAGACAAAGGCTGGAGCGCCCCAAAA ACTGGCTTAGAAGTCCCAGTCAATTCAGGGTGGCCTTAGCAGACAAAGGCTGGAGCGCCCCAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:173867847..173867925 26863196 MeRIP-seq:(Medium) rs1398509645 Functional Loss SNV dbSNP153 33..33 33 - - - 101935 RMVar_ID_101935 Human_SNP_ID_39237528 m1A Human chr1 + 173867927 173867927 173867927 GTGACCTTAGCAGACAAAGGCTGGAGCGCCCCAAAACCCGCAACATTCGCAAAGATAAAACATAC GTGACCTTAGCAGACAAAGGCTGGAGCGCCCCCAAACCCGCAACATTCGCAAAGATAAAACATAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:173867763..173867931 26863196 MeRIP-seq:(Medium) rs1342741268 Functional Loss SNV dbSNP153 33..33 33 - - - 101936 RMVar_ID_101936 Human_SNP_ID_39307209 m1A Human chr1 - 174159578 174159578 174159578 GCCCGCGTTCCACCCTCCACCTCGCGCTCTGAAGCCGGGCCGGTCCCGTTCGCTCCGCCACCGCT GCCCGCGTTCCACCCTCCACCTCGCGCTCTGACGCCGGGCCGGTCCCGTTCGCTCCGCCACCGCT T G RABGAP1L-DT Ensembl:ENSG00000227373 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:174159530..174159720 26863196 MeRIP-seq:(Medium) rs1224308845 Functional Loss SNV dbSNP153 33..33 33 - - - 101937 RMVar_ID_101937 Human_SNP_ID_39322125 m1A Human chr1 + 174219076 174219076 174219076 AAGCTTTATTAGTTCATGTTTTTAATTAGTTCATGTTTTTAATCAGTAGGTTTTTTTTTTTAATC AAGCTTTATTAGTTCATGTTTTTAATTAGTTCTTGTTTTTAATCAGTAGGTTTTTTTTTTTAATC A T RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:174219073..174219159 26863196 MeRIP-seq:(Medium) rs77087504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729 101938 RMVar_ID_101938 Human_SNP_ID_39322126 m1A Human chr1 - 174219079 174219079 174219079 AGGGATTAAAAAAAAAAACCTACTGATTAAAAACATGAACTAATTAAAAACATGAACTAATAAAG AGGGATTAAAAAAAAAAACCTACTGATTAAAAGCATGAACTAATTAAAAACATGAACTAATAAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:174219077..174219197 26863196 MeRIP-seq:(Medium) rs575028857 Functional Loss SNV dbSNP153 33..33 33 - - - 101939 RMVar_ID_101939 Human_SNP_ID_39518251 m1A Human chr1 + 175000066 175000066 175000066 TCTTGCGCAGGGTCGGTGTGGGCGCAGGCTGCAGCGCCGCGACTCGTGCGGGTAGGCGTCTGCGC TCTTGCGCAGGGTCGGTGTGGGCGCAGGCTGCGGCGCCGCGACTCGTGCGGGTAGGCGTCTGCGC A G CACYBP Ensembl:ENSG00000116161 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:174999964..175000140 26863410 MeRIP-seq:(Medium) rs755859164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333665,Human_RBP_ID_1416002,Human_RBP_ID_4009316,Human_RBP_ID_5458352,Human_RBP_ID_8755263,Human_RBP_ID_8940030,Human_RBP_ID_9270492,Human_RBP_ID_9319264,Human_RBP_ID_9357186,Human_RBP_ID_22427713,Human_RBP_ID_23346620,Human_RBP_ID_26312242,Human_RBP_ID_27801155,Human_RBP_ID_27835348 101940 RMVar_ID_101940 Human_SNP_ID_39518256 m1A Human chr1 + 175000075 175000075 175000075 GGGTCGGTGTGGGCGCAGGCTGCAGCGCCGCGACTCGTGCGGGTAGGCGTCTGCGCTCGGTTTGA GGGTCGGTGTGGGCGCAGGCTGCAGCGCCGCGGCTCGTGCGGGTAGGCGTCTGCGCTCGGTTTGA A G CACYBP Ensembl:ENSG00000116161 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:175000025..175000200 26863196 MeRIP-seq:(Medium) rs1182513264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333665,Human_RBP_ID_1416002,Human_RBP_ID_4009316,Human_RBP_ID_5458352,Human_RBP_ID_8755263,Human_RBP_ID_8940030,Human_RBP_ID_9270492,Human_RBP_ID_9319264,Human_RBP_ID_9357186,Human_RBP_ID_23346620,Human_RBP_ID_27835349 101941 RMVar_ID_101941 Human_SNP_ID_39518257 m1A Human chr1 + 175000075 175000075 175000075 GGGTCGGTGTGGGCGCAGGCTGCAGCGCCGCGACTCGTGCGGGTAGGCGTCTGCGCTCGGTTTGA GGGTCGGTGTGGGCGCAGGCTGCAGCGCCGCGTCTCGTGCGGGTAGGCGTCTGCGCTCGGTTTGA A T CACYBP Ensembl:ENSG00000116161 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:175000025..175000200 26863196 MeRIP-seq:(Medium) rs1182513264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333665,Human_RBP_ID_1416002,Human_RBP_ID_4009316,Human_RBP_ID_5458352,Human_RBP_ID_8755263,Human_RBP_ID_8940030,Human_RBP_ID_9270492,Human_RBP_ID_9319264,Human_RBP_ID_9357186,Human_RBP_ID_23346620,Human_RBP_ID_27835349 101942 RMVar_ID_101942 Human_SNP_ID_39518272 m1A Human chr1 - 175000099 175000099 175000099 AACAGGAAACCCCGCGCCGAGCCCTCAAACCGAGCGCAGACGCCTACCCGCACGAGTCGCGGCGC AACAGGAAACCCCGCGCCGAGCCCTCAAACCGTGCGCAGACGCCTACCCGCACGAGTCGCGGCGC T A lnc-MRPS14-1 RNACentral:URS00008B9216 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,Starvation treatment;HTR8/Svneo,Hypoxia IP chr1:174999998..175000148;chr1:175000001..175000100 26863410,32194978 MeRIP-seq:(Medium) rs938676835 Functional Loss SNV dbSNP153 33..33 33 - - - 101943 RMVar_ID_101943 Human_SNP_ID_39518273 m1A Human chr1 - 175000099 175000099 175000099 AACAGGAAACCCCGCGCCGAGCCCTCAAACCGAGCGCAGACGCCTACCCGCACGAGTCGCGGCGC AACAGGAAACCCCGCGCCGAGCCCTCAAACCGGGCGCAGACGCCTACCCGCACGAGTCGCGGCGC T C lnc-MRPS14-1 RNACentral:URS00008B9216 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,Starvation treatment;HTR8/Svneo,Hypoxia IP chr1:174999998..175000148;chr1:175000001..175000100 26863410,32194978 MeRIP-seq:(Medium) rs938676835 Functional Loss SNV dbSNP153 33..33 33 - - - 101944 RMVar_ID_101944 Human_SNP_ID_39518288 m1A Human chr1 - 175000130 175000130 175000130 AAGTCCCGAGCTGCAGCCGCGCAGAAGGAGGAACAGGAAACCCCGCGCCGAGCCCTCAAACCGAG AAGTCCCGAGCTGCAGCCGCGCAGAAGGAGGAGCAGGAAACCCCGCGCCGAGCCCTCAAACCGAG T C lnc-MRPS14-1 RNACentral:URS00008B9216 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:174999738..175000214;chr1:174999761..175000264;chr1:174999756..175000462 26863196 MeRIP-seq:(Medium) rs1264437435 Functional Loss SNV dbSNP153 33..33 33 - - - 101945 RMVar_ID_101945 Human_SNP_ID_39518292 m1A Human chr1 - 175000134 175000134 175000134 GCCGAAGTCCCGAGCTGCAGCCGCGCAGAAGGAGGAACAGGAAACCCCGCGCCGAGCCCTCAAAC GCCGAAGTCCCGAGCTGCAGCCGCGCAGAAGGCGGAACAGGAAACCCCGCGCCGAGCCCTCAAAC T G lnc-MRPS14-1 RNACentral:URS00008B9216 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:174999788..175000214 26863196 MeRIP-seq:(Medium) rs1364517640 Functional Loss SNV dbSNP153 33..33 33 - - - 101946 RMVar_ID_101946 Human_SNP_ID_39561702 m1A Human chr1 + 175166641 175166641 175166641 CCACGTTACTTCTTGCTTTGCGTTGTCAGGGGATCTCGGCCAGAACTGCTTTCCTGGAGGTCACG CCACGTTACTTCTTGCTTTGCGTTGTCAGGGGTTCTCGGCCAGAACTGCTTTCCTGGAGGTCACG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:175166592..175166666 26863196 MeRIP-seq:(Medium) rs1021270138 Functional Loss SNV dbSNP153 33..33 33 - - - 101947 RMVar_ID_101947 Human_SNP_ID_39567474 m1A Human chr1 + 175192721 175192720 175192721 GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGGAGGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGG_GGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:175192651..175192763 26863196 MeRIP-seq:(Medium) rs754362769 Functional Loss DEL dbSNP153 33..33 33 - - - 101948 RMVar_ID_101948 Human_SNP_ID_39567475 m1A Human chr1 + 175192721 175192721 175192721 GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGGAGGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGGCGGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:175192651..175192763 26863196 MeRIP-seq:(Medium) rs1431943574 Functional Loss SNV dbSNP153 33..33 33 - - - 101949 RMVar_ID_101949 Human_SNP_ID_39567476 m1A Human chr1 + 175192721 175192721 175192721 GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGGAGGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG GCTGCCCCGTCTGACAGCGCCCCGGGCCCTGGGGGGAGGTGTGGGTTCCTTTTTGGTTGCCTCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:175192651..175192763 26863196 MeRIP-seq:(Medium) rs1431943574 Functional Loss SNV dbSNP153 33..33 33 - - - 101950 RMVar_ID_101950 Human_SNP_ID_39567656 m1A Human chr1 - 175193066 175193066 175193066 GAGGGAGGGCGCGTCTGGGGCGTGTGCGCCCAAGGCCAGAGGCACCCGAGGTGGGCTGGCCCAGG GAGGGAGGGCGCGTCTGGGGCGTGTGCGCCCAGGGCCAGAGGCACCCGAGGTGGGCTGGCCCAGG T C lnc-KIAA0040-2 RNACentral:URS00009AFD32 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:175193022..175193096 26863196 MeRIP-seq:(Medium) rs1466195834 Functional Loss SNV dbSNP153 33..33 33 - - - 101951 RMVar_ID_101951 Human_SNP_ID_39567657 m1A Human chr1 - 175193066 175193066 175193066 GAGGGAGGGCGCGTCTGGGGCGTGTGCGCCCAAGGCCAGAGGCACCCGAGGTGGGCTGGCCCAGG GAGGGAGGGCGCGTCTGGGGCGTGTGCGCCCACGGCCAGAGGCACCCGAGGTGGGCTGGCCCAGG T G lnc-KIAA0040-2 RNACentral:URS00009AFD32 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:175193022..175193096 26863196 MeRIP-seq:(Medium) rs1466195834 Functional Loss SNV dbSNP153 33..33 33 - - - 101952 RMVar_ID_101952 Human_SNP_ID_39784295 m1A Human chr1 + 176057343 176057315 176057344 ACCTCTCCCTCTCCCTCTCCCTCTCCCCACGGATTCCCTCTCCCTCTCTTTCCACGATCTCCCTC ACCTC_____________________________TCCCTCTCCCTCTCTTTCCACGATCTCCCTC CTCCCTCTCCCTCTCCCTCTCCCCACGGAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:176057292..176057397 26863196 MeRIP-seq:(Medium) rs1268986530 Functional Loss DEL dbSNP153 6..34 33 - - - 101953 RMVar_ID_101953 Human_SNP_ID_39784296 m1A Human chr1 + 176057343 176057321 176057344 ACCTCTCCCTCTCCCTCTCCCTCTCCCCACGGATTCCCTCTCCCTCTCTTTCCACGATCTCCCTC ACCTCTCCCTC_______________________TCCCTCTCCCTCTCTTTCCACGATCTCCCTC CTCCCTCTCCCTCTCCCCACGGAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:176057292..176057397 26863196 MeRIP-seq:(Medium) rs1341735133 Functional Loss DEL dbSNP153 12..34 33 - - - 101954 RMVar_ID_101954 Human_SNP_ID_39822264 m1A Human chr1 - 176206657 176206657 176206657 CCGGCGTAGGAGGCAGCAGCTCCAGCCTAGGCAGCGGCAGCAGGAAGCGACCTCTCCTCGCCCCC CCGGCGTAGGAGGCAGCAGCTCCAGCCTAGGCGGCGGCAGCAGGAAGCGACCTCTCCTCGCCCCC T C COP1 Ensembl:ENSG00000143207 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:176206608..176206767 26863196 MeRIP-seq:(Medium) rs553749276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_160195,Human_Splice_Rec_160229,Human_Splice_Rec_160301,Human_Splice_Rec_160343,Human_Splice_Rec_160427 Human_miRNA_ID_2510523,Human_miRNA_ID_3053345 RMVar_hsa_circ_107818,RMVar_hsa_circ_137851 101955 RMVar_ID_101955 Human_SNP_ID_39822294 m1A Human chr1 - 176206713 176206713 176206713 CGGCGGGGCGGTGTCCACGGGCCTGTCCCGGCACAGCTGCGCGGCCAGGCCCAGCGCCGGCGTAG CGGCGGGGCGGTGTCCACGGGCCTGTCCCGGCCCAGCTGCGCGGCCAGGCCCAGCGCCGGCGTAG T G COP1 Ensembl:ENSG00000143207 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:176206664..176206792 26863196 MeRIP-seq:(Medium) rs1304985038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107818,RMVar_hsa_circ_137851 101956 RMVar_ID_101956 Human_SNP_ID_39822300 m1A Human chr1 + 176206722 176206722 176206722 CGCTGGGCCTGGCCGCGCAGCTGTGCCGGGACAGGCCCGTGGACACCGCCCCGCCGCCGCTACCC CGCTGGGCCTGGCCGCGCAGCTGTGCCGGGACGGGCCCGTGGACACCGCCCCGCCGCCGCTACCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T cell line,total RNA;HEK293T,H2O2 treatment chr1:176206672..176206786;chr1:176206642..176206743 26863196,26863410 MeRIP-seq:(Medium) rs1431484004 Functional Loss SNV dbSNP153 33..33 33 - - - 101957 RMVar_ID_101957 Human_SNP_ID_39822319 m1A Human chr1 - 176206750 176206750 176206750 GGCCTGTGTTGGTGGCGCCCGCCGTATCGGGTAGCGGCGGCGGGGCGGTGTCCACGGGCCTGTCC GGCCTGTGTTGGTGGCGCCCGCCGTATCGGGTGGCGGCGGCGGGGCGGTGTCCACGGGCCTGTCC T C COP1 Ensembl:ENSG00000143207 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:176206653..176206993 26863410 MeRIP-seq:(Medium) rs1187722425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8755264 RMVar_hsa_circ_107818,RMVar_hsa_circ_137851 101958 RMVar_ID_101958 Human_SNP_ID_40269772 m1A Human chr1 + 178093801 178093792 178093801 CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCACCGCCACCGCCACCGCCGTGGCTGCC CCGCTGCCGCCGCCGCCGCCGCCG_________CCGCCACCGCCACCGCCACCGCCGTGGCTGCC GCCACCGCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:178093752..178094213 26863196 MeRIP-seq:(Medium) rs1558048722 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 101959 RMVar_ID_101959 Human_SNP_ID_40269790 m1A Human chr1 + 178093801 178093798 178093801 CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCACCGCCACCGCCACCGCCGTGGCTGCC CCGCTGCCGCCGCCGCCGCCGCCGCCACCG___CCGCCACCGCCACCGCCACCGCCGTGGCTGCC GCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:178093752..178094213 26863196 MeRIP-seq:(Medium) rs1278121451 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 101960 RMVar_ID_101960 Human_SNP_ID_40269791 m1A Human chr1 + 178093801 178093801 178093801 CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCACCGCCACCGCCACCGCCGTGGCTGCC CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCACCGCCACCGCCACCGCCGTGGCTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:178093752..178094213 26863196 MeRIP-seq:(Medium) rs557601483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 101961 RMVar_ID_101961 Human_SNP_ID_40269801 m1A Human chr1 + 178093819 178093819 178093819 CCGCCGCCACCGCCACCGCCACCGCCACCGCCACCGCCGTGGCTGCCGGGTTTGTGGGATCCGCC CCGCCGCCACCGCCACCGCCACCGCCACCGCCGCCGCCGTGGCTGCCGGGTTTGTGGGATCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:178093689..178093996;chr1:178093774..178093903;chr1:178093705..178093886;chr1:178093689..178094230;chr1:178093689..178094217 26863196 MeRIP-seq:(Medium) rs1200781664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 101962 RMVar_ID_101962 Human_SNP_ID_40276000 m1A Human chr1 - 178119857 178119857 178119857 GGGTGGCATGTGTTCCTCTTTTGGCTAGCACCATAACTAGATGAATTGAGGAAATAGCAGAGGAT GGGTGGCATGTGTTCCTCTTTTGGCTAGCACCTTAACTAGATGAATTGAGGAAATAGCAGAGGAT T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:178119752..178119896 26863196 MeRIP-seq:(Medium) rs540277132 Functional Loss SNV dbSNP153 33..33 33 - - - 101963 RMVar_ID_101963 Human_SNP_ID_40276001 m1A Human chr1 - 178119857 178119857 178119857 GGGTGGCATGTGTTCCTCTTTTGGCTAGCACCATAACTAGATGAATTGAGGAAATAGCAGAGGAT GGGTGGCATGTGTTCCTCTTTTGGCTAGCACCGTAACTAGATGAATTGAGGAAATAGCAGAGGAT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:178119752..178119896 26863196 MeRIP-seq:(Medium) rs540277132 Functional Loss SNV dbSNP153 33..33 33 - - - 101964 RMVar_ID_101964 Human_SNP_ID_40314782 m1A Human chr1 - 178286977 178286977 178286977 TCCTAGGTCTCAGAAGGGTTGAAGGATTGCTGAAATAAGAAATGAGCTAGAAAGATAGAAGGTAT TCCTAGGTCTCAGAAGGGTTGAAGGATTGCTGGAATAAGAAATGAGCTAGAAAGATAGAAGGTAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:178286859..178286986 26863196 MeRIP-seq:(Medium) rs1370584054 Functional Loss SNV dbSNP153 33..33 33 - - - 101965 RMVar_ID_101965 Human_SNP_ID_40342524 m1A Human chr1 + 178410095 178410095 178410095 GATGATTAGCTGTGGAATCTAGGGAGAAGGAAAAGAGAGCAGGAAAAAACAAGGGACAGGGAGAA GATGATTAGCTGTGGAATCTAGGGAGAAGGAAGAGAGAGCAGGAAAAAACAAGGGACAGGGAGAA A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:178410090..178410259 26863196 MeRIP-seq:(Medium) rs1330149268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26870,RMVar_hsa_circ_109987,RMVar_hsa_circ_297513,RMVar_hsa_circ_271955,RMVar_hsa_circ_126428,RMVar_hsa_circ_70365,RMVar_hsa_circ_29305,RMVar_hsa_circ_137896,RMVar_hsa_circ_137897,RMVar_hsa_circ_137895,RMVar_hsa_circ_137902,RMVar_hsa_circ_9266,RMVar_hsa_circ_123237,RMVar_hsa_circ_137900,RMVar_hsa_circ_121467,RMVar_hsa_circ_137903 101966 RMVar_ID_101966 Human_SNP_ID_40373449 m1A Human chr1 - 178542955 178542955 178542955 TGGGTGGGCCTCTCACCCCAGACGGCGGCCGCAGCCCGTCCCTGATCACCGGCCGCCTGAGCCCT TGGGTGGGCCTCTCACCCCAGACGGCGGCCGCTGCCCGTCCCTGATCACCGGCCGCCTGAGCCCT T A lnc-CLEC20A-8 RNACentral:URS00008B98C7 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:178542915..178542986 26863196 MeRIP-seq:(Medium) rs1381462253 Functional Loss SNV dbSNP153 33..33 33 - - - 101967 RMVar_ID_101967 Human_SNP_ID_40438256 m1A Human chr1 + 178812203 178812203 178812203 CTTCTTCACTGGGGAGAGGGGAGTTTTGGGGGAGGGGGTACATAAGAGTAAGTGATTTTCAGGTA CTTCTTCACTGGGGAGAGGGGAGTTTTGGGGGTGGGGGTACATAAGAGTAAGTGATTTTCAGGTA A T RALGPS2 Ensembl:ENSG00000116191 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:178812189..178812316 26863196 MeRIP-seq:(Medium) rs1203316733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23882,RMVar_hsa_circ_16756,RMVar_hsa_circ_348611,RMVar_hsa_circ_80411,RMVar_hsa_circ_272141,RMVar_hsa_circ_137910,RMVar_hsa_circ_137911,RMVar_hsa_circ_82734,RMVar_hsa_circ_350277,RMVar_hsa_circ_275117,RMVar_hsa_circ_41408,RMVar_hsa_circ_56434,RMVar_hsa_circ_137913,RMVar_hsa_circ_324322,RMVar_hsa_circ_60395,RMVar_hsa_circ_127297,RMVar_hsa_circ_37720,RMVar_hsa_circ_82000,RMVar_hsa_circ_137914,RMVar_hsa_circ_137915,RMVar_hsa_circ_137916,RMVar_hsa_circ_117851,RMVar_hsa_circ_137917,RMVar_hsa_circ_137918 101968 RMVar_ID_101968 Human_SNP_ID_40489605 m1A Human chr1 - 179025994 179025975 179025994 CCTCCGGGGAGGGGCAGCCCCACGCCGCGCTCACCGCCCCCAGCCGCCGCCGCCGCCACAGCGGC CCTCCGGGGAGGGGCAGCCCCACGCCGCGCTC___________________GCCGCCACAGCGGC CGGCGGCGGCTGGGGGCGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:179025890..179026207;chr1:179025911..179026219 26863196 MeRIP-seq:(Medium) rs918020697 Functional Loss DEL dbSNP153 33..51 33 - - - 101969 RMVar_ID_101969 Human_SNP_ID_40489616 m1A Human chr1 - 179025994 179025994 179025994 CCTCCGGGGAGGGGCAGCCCCACGCCGCGCTCACCGCCCCCAGCCGCCGCCGCCGCCACAGCGGC CCTCCGGGGAGGGGCAGCCCCACGCCGCGCTCCCCGCCCCCAGCCGCCGCCGCCGCCACAGCGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:179025890..179026207;chr1:179025911..179026219 26863196 MeRIP-seq:(Medium) rs990722424 Functional Loss SNV dbSNP153 33..33 33 - - - 101970 RMVar_ID_101970 Human_SNP_ID_40489645 m1A Human chr1 + 179026097 179026097 179026097 CGGGCGGCCATGGAGCGAGCCTAGGGCCCGACAGGTGAGTGGCGCGGGGGCGGGGGAGGGCGCGC CGGGCGGCCATGGAGCGAGCCTAGGGCCCGACGGGTGAGTGGCGCGGGGGCGGGGGAGGGCGCGC A G FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:179025997..179026104 26863410 MeRIP-seq:(Medium) rs1167746334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073174,Human_RBP_ID_5312761,Human_RBP_ID_22707175 Human_Splice_Rec_161633 RMVar_hsa_circ_77766,RMVar_hsa_circ_137937 101971 RMVar_ID_101971 Human_SNP_ID_40492273 m1A Human chr1 + 179036923 179036923 179036923 GCTCAGACTTTATCAGGAGGAGATTGGAAGAAATGTTAAGAGAAAGAGGAATTTTGAGGGACTAC GCTCAGACTTTATCAGGAGGAGATTGGAAGAACTGTTAAGAGAAAGAGGAATTTTGAGGGACTAC A C FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:179036920..179037030 26863196 MeRIP-seq:(Medium) rs1177659515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77766,RMVar_hsa_circ_137937 101972 RMVar_ID_101972 Human_SNP_ID_40501660 m1A Human chr1 + 179075117 179075117 179075117 GGGAGGCTGAGGCAGGAGAATCACTTGAATCCAGGAGGCGAAGGTTGCAGTGAGCTGAGATTGTG GGGAGGCTGAGGCAGGAGAATCACTTGAATCCGGGAGGCGAAGGTTGCAGTGAGCTGAGATTGTG A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1225045270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 101973 RMVar_ID_101973 Human_SNP_ID_40503608 m1A Human chr1 + 179082129 179082129 179082129 CAGCCGGATGGTCCCGCAGCTCGGGGCCGGCCATGCTTCGCGGTCCGTGGCGCCAGCTTTGGCTC CAGCCGGATGGTCCCGCAGCTCGGGGCCGGCCGTGCTTCGCGGTCCGTGGCGCCAGCTTTGGCTC A G TOR3A Ensembl:ENSG00000186283 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:179082080..179082182 26863196 MeRIP-seq:(Medium) rs1209208923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223013,Human_RBP_ID_803030,Human_RBP_ID_4010128,Human_RBP_ID_8754259,Human_RBP_ID_27391514 RMVar_hsa_circ_87338,RMVar_hsa_circ_137947 101974 RMVar_ID_101974 Human_SNP_ID_40503609 m1A Human chr1 + 179082129 179082129 179082129 CAGCCGGATGGTCCCGCAGCTCGGGGCCGGCCATGCTTCGCGGTCCGTGGCGCCAGCTTTGGCTC CAGCCGGATGGTCCCGCAGCTCGGGGCCGGCCTTGCTTCGCGGTCCGTGGCGCCAGCTTTGGCTC A T TOR3A Ensembl:ENSG00000186283 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:179082080..179082182 26863196 MeRIP-seq:(Medium) rs1209208923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223013,Human_RBP_ID_803030,Human_RBP_ID_4010128,Human_RBP_ID_8754259,Human_RBP_ID_27391514 RMVar_hsa_circ_87338,RMVar_hsa_circ_137947 101975 RMVar_ID_101975 Human_SNP_ID_40503640 m1A Human chr1 - 179082169 179082169 179082169 CGCGGGGCTCAGGCGCGCCCGGGAGCAGCAGCAGGAAAAAGAGCCAAAGCTGGCGCCACGGACCG CGCGGGGCTCAGGCGCGCCCGGGAGCAGCAGCGGGAAAAAGAGCCAAAGCTGGCGCCACGGACCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:179082071..179082325 26863410 MeRIP-seq:(Medium) rs897210417 Functional Loss SNV dbSNP153 33..33 33 - - - 101976 RMVar_ID_101976 Human_SNP_ID_40503720 m1A Human chr1 - 179082301 179082301 179082301 GGCAGCTGAAGAGCGTCCAGTACCGCTTGGAGAGGGCACCCGCCGCCCTGAGCTGCTCCTGCAGG GGCAGCTGAAGAGCGTCCAGTACCGCTTGGAGGGGGCACCCGCCGCCCTGAGCTGCTCCTGCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:179082120..179082848 32194978 MeRIP-seq:(Medium) rs1184956678 Functional Loss SNV dbSNP153 33..33 33 - - - 101977 RMVar_ID_101977 Human_SNP_ID_40506476 m1A Human chr1 + 179091360 179091360 179091360 TGAGGTGCTCCAGAAAGACAGTGTCTGTCTAAAGGTAGAACGCTGGTGCCAGAGTGGTGGTCCTG TGAGGTGCTCCAGAAAGACAGTGTCTGTCTAAGGGTAGAACGCTGGTGCCAGAGTGGTGGTCCTG A G TOR3A Ensembl:ENSG00000186283 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179091355..179091494 26863196 MeRIP-seq:(Medium) rs1190746831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10672928 RMVar_hsa_circ_269990,RMVar_hsa_circ_137949 101978 RMVar_ID_101978 Human_SNP_ID_40519946 m1A Human chr1 + 179140314 179140314 179140314 GGCTTTTCCTTTTGCCTAAAACACTCTTCCCCATGACATTTCACCAAATGTTACCTTCTCAGTAT GGCTTTTCCTTTTGCCTAAAACACTCTTCCCCGTGACATTTCACCAAATGTTACCTTCTCAGTAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:179140311..179140395 26863196 MeRIP-seq:(Medium) rs1303989301 Functional Loss SNV dbSNP153 33..33 33 - - - 101979 RMVar_ID_101979 Human_SNP_ID_40540986 m1A Human chr1 - 179227330 179227329 179227330 GGAATGAAGCATCATTATGAGTTGGAAGAAAAAGATCATAGAGCAAAAATTGGAAGAGTCAAGTT GGAATGAAGCATCATTATGAGTTGGAAGAAAA_GATCATAGAGCAAAAATTGGAAGAGTCAAGTT CT C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179227328..179227485 26863196 MeRIP-seq:(Medium) rs1558012218 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5333968,Human_RBP_ID_10675740 RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 101980 RMVar_ID_101980 Human_SNP_ID_40540987 m1A Human chr1 - 179227330 179227330 179227330 GGAATGAAGCATCATTATGAGTTGGAAGAAAAAGATCATAGAGCAAAAATTGGAAGAGTCAAGTT GGAATGAAGCATCATTATGAGTTGGAAGAAAACGATCATAGAGCAAAAATTGGAAGAGTCAAGTT T G ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179227328..179227485 26863196 MeRIP-seq:(Medium) rs1464542881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5333968,Human_RBP_ID_10675740 RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 101981 RMVar_ID_101981 Human_SNP_ID_40541408 m1A Human chr1 + 179228825 179228825 179228825 TGTACTCCACAATCTCCTGAAATTCAGTTCCCATTTCCCAATCCCTTAGGATACAACCCATTTCC TGTACTCCACAATCTCCTGAAATTCAGTTCCCGTTTCCCAATCCCTTAGGATACAACCCATTTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179228821..179229151 26863196 MeRIP-seq:(Medium) rs1376226781 Functional Loss SNV dbSNP153 33..33 33 - - - 101982 RMVar_ID_101982 Human_SNP_ID_40541673 m1A Human chr1 - 179229462 179229462 179229462 GAGGGAGAGACCGGAGCAGCGCCAGGAGCCCGAGGCCGGAGCCGAGGAGGAATGTGACCAGGGGT GAGGGAGAGACCGGAGCAGCGCCAGGAGCCCGGGGCCGGAGCCGAGGAGGAATGTGACCAGGGGT T C ABL2 Ensembl:ENSG00000143322 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:179229326..179229625 26863196 MeRIP-seq:(Medium) rs1202490826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3328712,Human_RBP_ID_3934336,Human_RBP_ID_18187842,Human_RBP_ID_18415113,Human_RBP_ID_22870996,Human_RBP_ID_26312251 RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 101983 RMVar_ID_101983 Human_SNP_ID_40558010 m1A Human chr1 - 179293859 179293859 179293859 GCCGGGAAGCGGTCACAGAGCAGCCAGCAGGAAGGTCGACTCCGGGAAGCTCTCCTGGCGCCCAG GCCGGGAAGCGGTCACAGAGCAGCCAGCAGGAGGGTCGACTCCGGGAAGCTCTCCTGGCGCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179293785..179293990 26863196 MeRIP-seq:(Medium) rs374105663 Functional Loss SNV dbSNP153 33..33 33 - - - 101984 RMVar_ID_101984 Human_SNP_ID_40573395 m1A Human chr1 + 179354784 179354784 179354784 ATTATGTAATACTTCCATTTTATAAGATGCCCATTTCTAATACAATGTGTGTAGGAATTATTTGT ATTATGTAATACTTCCATTTTATAAGATGCCCGTTTCTAATACAATGTGTGTAGGAATTATTTGT A G SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4652366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10676243,Human_RBP_ID_22374036 Human_miRNA_ID_1655928 GWAS_ID_13397,GWAS_ID_13398,GWAS_ID_13399,GWAS_ID_13400,GWAS_ID_13401,GWAS_ID_13402,GWAS_ID_13403,GWAS_ID_13404 RMVar_hsa_circ_264822 101985 RMVar_ID_101985 Human_SNP_ID_40573396 m1A Human chr1 + 179354784 179354784 179354784 ATTATGTAATACTTCCATTTTATAAGATGCCCATTTCTAATACAATGTGTGTAGGAATTATTTGT ATTATGTAATACTTCCATTTTATAAGATGCCCTTTTCTAATACAATGTGTGTAGGAATTATTTGT A T SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4652366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10676243,Human_RBP_ID_22374036 Human_miRNA_ID_1655928 GWAS_ID_13397,GWAS_ID_13398,GWAS_ID_13399,GWAS_ID_13400,GWAS_ID_13401,GWAS_ID_13402,GWAS_ID_13403,GWAS_ID_13404 RMVar_hsa_circ_264822 101986 RMVar_ID_101986 Human_SNP_ID_40690876 m1A Human chr1 - 179846284 179846284 179846284 AAAGATGTGGCCCTGGTCCTGACTGTTCTGCTAGAGGAGGAAACATTAGAAGCAAGTGTAGGCCC AAAGATGTGGCCCTGGTCCTGACTGTTCTGCTGGAGGAGGAAACATTAGAAGCAAGTGTAGGCCC T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:179846234..179846328 26863196 MeRIP-seq:(Medium) rs201270641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_973225,Human_RBP_ID_1730492,Human_RBP_ID_3288650,Human_RBP_ID_5721812,Human_RBP_ID_10676852,Human_RBP_ID_22374120,Human_RBP_ID_23348762,Human_RBP_ID_27172284,Human_RBP_ID_27391639 Human_miRNA_ID_1772193 RMVar_hsa_circ_138015,RMVar_hsa_circ_138016 101987 RMVar_ID_101987 Human_SNP_ID_40699302 m1A Human chr1 - 179882333 179882332 179882334 CCGCCGCCTGCGTCGTCGCTGCTGTGTAGCAAACCTGCCTCTGGGCCCATGGTGTGTCTTGAGGG CCGCCGCCTGCGTCGTCGCTGCTGTGTAGCA__CCTGCCTCTGGGCCCATGGTGTGTCTTGAGGG GTT G AL353708.3 Ensembl:ENSG00000272906 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:179882149..179882546 26863196 MeRIP-seq:(Medium) rs1399968881 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10678022 101988 RMVar_ID_101988 Human_SNP_ID_40699303 m1A Human chr1 - 179882333 179882333 179882333 CCGCCGCCTGCGTCGTCGCTGCTGTGTAGCAAACCTGCCTCTGGGCCCATGGTGTGTCTTGAGGG CCGCCGCCTGCGTCGTCGCTGCTGTGTAGCAACCCTGCCTCTGGGCCCATGGTGTGTCTTGAGGG T G AL353708.3 Ensembl:ENSG00000272906 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:179882149..179882546 26863196 MeRIP-seq:(Medium) rs1016908291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10678022 101989 RMVar_ID_101989 Human_SNP_ID_40699560 m1A Human chr1 + 179882802 179882802 179882802 TTCCGGTCCGATTCTGCGAAAGAGGAAGTGAGAGAAAGCGCGTACTACCTTCGGTCTAGGCAGCG TTCCGGTCCGATTCTGCGAAAGAGGAAGTGAGGGAAAGCGCGTACTACCTTCGGTCTAGGCAGCG A G TOR1AIP1 Ensembl:ENSG00000143337 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179882751..179882892 26863196 MeRIP-seq:(Medium) rs571502268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17732591,Human_RBP_ID_18415687,Human_RBP_ID_26312252,Human_RBP_ID_27801163 Human_miRNA_ID_2167650,Human_miRNA_ID_2169174 RMVar_hsa_circ_86132,RMVar_hsa_circ_138020 101990 RMVar_ID_101990 Human_SNP_ID_40699639 m1A Human chr1 + 179882900 179882900 179882900 GAAGACGCGAAGGACTACCCGCCTTCAGCAGCAGCACTCAGAGCAGCCTCCGCTACAGCCGTCTC GAAGACGCGAAGGACTACCCGCCTTCAGCAGCGGCACTCAGAGCAGCCTCCGCTACAGCCGTCTC A G TOR1AIP1 Ensembl:ENSG00000143337 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:179882851..179882975 32194978 MeRIP-seq:(Medium) rs772217777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9271652,Human_RBP_ID_9357204,Human_RBP_ID_18415687,Human_RBP_ID_22428729,Human_RBP_ID_26312252 Human_Splice_Rec_162481,Human_Splice_Rec_162499,Human_Splice_Rec_162519,Human_Splice_Rec_162537,Human_Splice_Rec_162555,Human_Splice_Rec_162569 Human_miRNA_ID_2712358,Human_miRNA_ID_2773208,Human_miRNA_ID_2906198,Human_miRNA_ID_3025026,Human_miRNA_ID_3048341 RMVar_hsa_circ_86132,RMVar_hsa_circ_138020 101991 RMVar_ID_101991 Human_SNP_ID_40716651 m1A Human chr1 - 179954898 179954898 179954898 GGCAAGCCACCCCCCGAGCTGCGGCTCCCTGCAGTTCTCTCTGGCGCAGGTCTGGCCCCGCTCCC GGCAAGCCACCCCCCGAGCTGCGGCTCCCTGCTGTTCTCTCTGGCGCAGGTCTGGCCCCGCTCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:179954849..179954941 26863196 MeRIP-seq:(Medium) rs1326386993 Functional Loss SNV dbSNP153 33..33 33 - - - 101992 RMVar_ID_101992 Human_SNP_ID_40720730 m1A Human chr1 + 179972345 179972345 179972345 TTCAAGGTTTAAAAGGCATATGGAGAAAGACTAGCTAGTAAAGGAGACTGAGAAAGAGAACTAGA TTCAAGGTTTAAAAGGCATATGGAGAAAGACTGGCTAGTAAAGGAGACTGAGAAAGAGAACTAGA A G CEP350 Ensembl:ENSG00000135837 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:179972342..179972467 26863196 MeRIP-seq:(Medium) rs969779869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9471213,Human_RBP_ID_10678926,Human_RBP_ID_23348961 101993 RMVar_ID_101993 Human_SNP_ID_127844919 m1A Human chr3 + 30606575 30606575 30606575 GCTGTTGGCGAGGAGTTTCCTGTTTCCCCCGCAGCGCTGAGTTGAAGTTGAGTGAGTCACTCGCG GCTGTTGGCGAGGAGTTTCCTGTTTCCCCCGCTGCGCTGAGTTGAAGTTGAGTGAGTCACTCGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:30606525..30606743 26863196 MeRIP-seq:(Medium) rs767704668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757819 RMVar_hsa_circ_105592,RMVar_hsa_circ_216605 101994 RMVar_ID_101994 Human_SNP_ID_127844926 m1A Human chr3 - 30606595 30606595 30606595 GGGTGTCGTCGCTCCGTGCGCGCGAGTGACTCACTCAACTTCAACTCAGCGCTGCGGGGGAAACA GGGTGTCGTCGCTCCGTGCGCGCGAGTGACTCGCTCAACTTCAACTCAGCGCTGCGGGGGAAACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:30606544..30606680 26863196 MeRIP-seq:(Medium) rs1223843606 Functional Loss SNV dbSNP153 33..33 33 - - - 101995 RMVar_ID_101995 Human_SNP_ID_127844951 m1A Human chr3 - 30606635 30606635 30606635 ACAGGAGTCCGGCTCCTGTCCCGAGCGGGTGCACGCGCGGGGGTGTCGTCGCTCCGTGCGCGCGA ACAGGAGTCCGGCTCCTGTCCCGAGCGGGTGCCCGCGCGGGGGTGTCGTCGCTCCGTGCGCGCGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:30606589..30606687 26863196 MeRIP-seq:(Medium) rs886058299 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_626 101996 RMVar_ID_101996 Human_SNP_ID_128082486 m1A Human chr3 - 31532769 31532769 31532769 AGCAGCGGCCGCAATCGCCGCTCTCTCAACCCAGATGGCCCCGGCGCCCCACTAGCCATCCGTAT AGCAGCGGCCGCAATCGCCGCTCTCTCAACCCGGATGGCCCCGGCGCCCCACTAGCCATCCGTAT T C lnc-OSBPL10-3 RNACentral:URS00008B4856 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:31532718..31532822 32194978 MeRIP-seq:(Medium) rs900033572 Functional Loss SNV dbSNP153 33..33 33 - - - 101997 RMVar_ID_101997 Human_SNP_ID_128082491 m1A Human chr3 - 31532788 31532788 31532788 GGCGGGGAGTCTCCGCCTCAGCAGCGGCCGCAATCGCCGCTCTCTCAACCCAGATGGCCCCGGCG GGCGGGGAGTCTCCGCCTCAGCAGCGGCCGCAGTCGCCGCTCTCTCAACCCAGATGGCCCCGGCG T C lnc-OSBPL10-3 RNACentral:URS00008B4856 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:31532687..31532787 26863410 MeRIP-seq:(Medium) rs1419161090 Functional Loss SNV dbSNP153 33..33 33 - - - 101998 RMVar_ID_101998 Human_SNP_ID_128082558 m1A Human chr3 - 31532908 31532908 31532908 GGTGCTGGGCGGGGACCCGGAGGAGGAGGAGGAGGAGGAAGAAAAAGGAGGAGGGAAGAGCTCTG GGTGCTGGGCGGGGACCCGGAGGAGGAGGAGGGGGAGGAAGAAAAAGGAGGAGGGAAGAGCTCTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:31532808..31533037 26863410 MeRIP-seq:(Medium) rs1359873679 Functional Loss SNV dbSNP153 33..33 33 - - - 101999 RMVar_ID_101999 Human_SNP_ID_128082662 m1A Human chr3 - 31533042 31533042 31533042 GGGCCATGAGGCCACTCCACGGGGACGAGTTGAGGGACGACTTGTGCTTGCTCTCCGGGGCCGAG GGGCCATGAGGCCACTCCACGGGGACGAGTTGCGGGACGACTTGTGCTTGCTCTCCGGGGCCGAG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:31532926..31533225 26863196 MeRIP-seq:(Medium) rs745544339 Functional Loss SNV dbSNP153 33..33 33 - - - 102000 RMVar_ID_102000 Human_SNP_ID_128082740 m1A Human chr3 - 31533196 31533196 31533196 AGGATGGTGAAGGAGAGAAGCGACTGCCACCCAGCCGGCTGCGACAGCCCCCCGGACAGCCCCGC AGGATGGTGAAGGAGAGAAGCGACTGCCACCCGGCCGGCTGCGACAGCCCCCCGGACAGCCCCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:31532829..31533250 26863196 MeRIP-seq:(Medium) rs760572215 Functional Loss SNV dbSNP153 33..33 33 - - - 102001 RMVar_ID_102001 Human_SNP_ID_128112022 m1A Human chr3 + 31648623 31648623 31648623 TTCACCTCCCCCTGACCCTGTGCCACAGCGTCACAGTACACAATCCAAGGACCAAAGGATTGCTT TTCACCTCCCCCTGACCCTGTGCCACAGCGTCTCAGTACACAATCCAAGGACCAAAGGATTGCTT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:31648585..31648886 26863196 MeRIP-seq:(Medium) rs1052100407 Functional Loss SNV dbSNP153 33..33 33 - - - 102002 RMVar_ID_102002 Human_SNP_ID_128112076 m1A Human chr3 - 31648795 31648791 31648796 AGGTTCTTGGTCCCCTGGGTGGCTGGCATGGCATGGGCAATGACGGGAATAGTGGTAGGACAACA AGGTTCTTGGTCCCCTGGGTGGCTGGCATGG_____GCAATGACGGGAATAGTGGTAGGACAACA CCCATG C lnc-OSBPL10-6 RNACentral:URS0000D5C892 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:31648697..31648839 26863196 MeRIP-seq:(Medium) rs935224192 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_18004087 102003 RMVar_ID_102003 Human_SNP_ID_128125609 m1A Human chr3 - 31701140 31701140 31701140 GAGGAATTCTTTGAGGAGGAAGATGACAGAACAGAGTGACTAACCATTTATAGAAGACAGGAGAG GAGGAATTCTTTGAGGAGGAAGATGACAGAACGGAGTGACTAACCATTTATAGAAGACAGGAGAG T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:31701089..31701250 26863196 MeRIP-seq:(Medium) rs1313876430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21563,RMVar_hsa_circ_60595,RMVar_hsa_circ_103022,RMVar_hsa_circ_216638,RMVar_hsa_circ_40000,RMVar_hsa_circ_323878,RMVar_hsa_circ_340764,RMVar_hsa_circ_216639 102004 RMVar_ID_102004 Human_SNP_ID_128174943 m1A Human chr3 + 31885373 31885373 31885373 AGTGTGACACACTCACACATTCATAACCACCCATGCACTCACCCTTGAAGGTGCATTTGCATATT AGTGTGACACACTCACACATTCATAACCACCCGTGCACTCACCCTTGAAGGTGCATTTGCATATT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:31885369..31885490 26863196 MeRIP-seq:(Medium) rs1187194728 Functional Loss SNV dbSNP153 33..33 33 - - - 102005 RMVar_ID_102005 Human_SNP_ID_128188899 m1A Human chr3 + 31938826 31938826 31938826 AGAGGCTTTTTCAAACCTCCTCGACTTTGCCCAAGCCTCAGGGTCCACCATCAACCCTTCCTCTA AGAGGCTTTTTCAAACCTCCTCGACTTTGCCCCAGCCTCAGGGTCCACCATCAACCCTTCCTCTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:31938814..31939097 26863196 MeRIP-seq:(Medium) rs1328785607 Functional Loss SNV dbSNP153 33..33 33 - - - 102006 RMVar_ID_102006 Human_SNP_ID_128188909 m1A Human chr3 - 31938866 31938866 31938866 CTGTAAAGTAGGAGGTGAGGTTATCGTCTGAGAGTGGAGTTAGAGGAAGGGTTGATGGTGGACCC CTGTAAAGTAGGAGGTGAGGTTATCGTCTGAGGGTGGAGTTAGAGGAAGGGTTGATGGTGGACCC T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:31938863..31939132 26863196 MeRIP-seq:(Medium) rs1468741371 Functional Loss SNV dbSNP153 33..33 33 - - - 102007 RMVar_ID_102007 Human_SNP_ID_128200057 m1A Human chr3 - 31981021 31981021 31981021 CGGTCGGCGGCGGCCGGGCTCGGCGGCGGGGGAAGCCGCAGCAGCCCGGGCTCTGTGGCCGCTAG CGGTCGGCGGCGGCCGGGCTCGGCGGCGGGGGGAGCCGCAGCAGCCCGGGCTCTGTGGCCGCTAG T C OSBPL10 Ensembl:ENSG00000144645 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:31980970..31981264 26863196 MeRIP-seq:(Medium) rs1050361341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756359,Human_RBP_ID_9354375 102008 RMVar_ID_102008 Human_SNP_ID_128200144 m1A Human chr3 - 31981205 31981190 31981205 GCCGCCGTGCCGGGGCCGCCACCGCGGCGGGCACCCGCGTCCCGGGCGCCCACGGACCATGGAGA GCCGCCGTGCCGGGGCCGCCACCGCGGCGGGC_______________GCCCACGGACCATGGAGA CGCCCGGGACGCGGGT C OSBPL10 Ensembl:ENSG00000144645 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:31981156..31981269;chr3:31981159..31981274 26863196 MeRIP-seq:(Medium) rs1297629742 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_4757832,Human_RBP_ID_8729750,Human_RBP_ID_18423939 102009 RMVar_ID_102009 Human_SNP_ID_128229533 m1A Human chr3 + 32106682 32106682 32106682 ACAGGCGGAGGTGGGCAGCCGGCCAGGGAAGCACGGTCCAGGCGGCTACATTCGGCCCGGCCATG ACAGGCGGAGGTGGGCAGCCGGCCAGGGAAGCGCGGTCCAGGCGGCTACATTCGGCCCGGCCATG A G GPD1L Ensembl:ENSG00000152642 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:32106557..32128178 26863196 MeRIP-seq:(Medium) rs774562002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757060,Human_RBP_ID_22605379 Human_Splice_Rec_405497,Human_Splice_Rec_405507,Human_Splice_Rec_405521 102010 RMVar_ID_102010 Human_SNP_ID_128229551 m1A Human chr3 + 32106712 32106712 32106712 GCACGGTCCAGGCGGCTACATTCGGCCCGGCCATGGCAGCGGCGCCCCTGAAAGTGTGCATCGTG GCACGGTCCAGGCGGCTACATTCGGCCCGGCCGTGGCAGCGGCGCCCCTGAAAGTGTGCATCGTG A G GPD1L Ensembl:ENSG00000152642 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:32106551..32128123 26863196 MeRIP-seq:(Medium) rs148643167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_599901,Human_RBP_ID_4757060 Human_Splice_Rec_405497,Human_Splice_Rec_405507,Human_Splice_Rec_405521 102011 RMVar_ID_102011 Human_SNP_ID_128244149 m1A Human chr3 + 32166114 32166113 32166115 GTACTGGGCAGTAACTAAACACACATGCAAACATGTGAATGGTGGTTTATTCCTCATTCTGTGGA GTACTGGGCAGTAACTAAACACACATGCAAAC__GTGAATGGTGGTTTATTCCTCATTCTGTGGA CAT C GPD1L Ensembl:ENSG00000152642 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1188115853 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23213075,Human_RBP_ID_26507238 Human_miRNA_ID_218182,Human_miRNA_ID_663214,Human_miRNA_ID_669399,Human_miRNA_ID_674013 102012 RMVar_ID_102012 Human_SNP_ID_128244150 m1A Human chr3 + 32166114 32166114 32166114 GTACTGGGCAGTAACTAAACACACATGCAAACATGTGAATGGTGGTTTATTCCTCATTCTGTGGA GTACTGGGCAGTAACTAAACACACATGCAAACGTGTGAATGGTGGTTTATTCCTCATTCTGTGGA A G GPD1L Ensembl:ENSG00000152642 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6799559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23213075,Human_RBP_ID_26507238 Human_miRNA_ID_218182,Human_miRNA_ID_663214,Human_miRNA_ID_669399,Human_miRNA_ID_674013 Clinvar_Rec_627 GWAS_ID_13405 102013 RMVar_ID_102013 Human_SNP_ID_128332001 m1A Human chr3 - 32529546 32529546 32529546 TTCCTGCTGGGTCAAAAAAAATTGATCCAAACATGAAAGGTACATCTCTTTCTAGGAGATAACAA TTCCTGCTGGGTCAAAAAAAATTGATCCAAACGTGAAAGGTACATCTCTTTCTAGGAGATAACAA T C DYNC1LI1 Ensembl:ENSG00000144635 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:32529542..32530365 32194978 MeRIP-seq:(Medium) rs1221449021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26823678 Human_Splice_Rec_405623,Human_Splice_Rec_405643,Human_Splice_Rec_405663 RMVar_hsa_circ_216662,RMVar_hsa_circ_322819,RMVar_hsa_circ_330317,RMVar_hsa_circ_272994,RMVar_hsa_circ_289025,RMVar_hsa_circ_113704,RMVar_hsa_circ_216664,RMVar_hsa_circ_216666,RMVar_hsa_circ_216665,RMVar_hsa_circ_216663,RMVar_hsa_circ_267055,RMVar_hsa_circ_269222 102014 RMVar_ID_102014 Human_SNP_ID_128332002 m1A Human chr3 - 32529546 32529546 32529546 TTCCTGCTGGGTCAAAAAAAATTGATCCAAACATGAAAGGTACATCTCTTTCTAGGAGATAACAA TTCCTGCTGGGTCAAAAAAAATTGATCCAAACCTGAAAGGTACATCTCTTTCTAGGAGATAACAA T G DYNC1LI1 Ensembl:ENSG00000144635 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:32529542..32530365 32194978 MeRIP-seq:(Medium) rs1221449021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26823678 Human_Splice_Rec_405623,Human_Splice_Rec_405643,Human_Splice_Rec_405663 RMVar_hsa_circ_216662,RMVar_hsa_circ_322819,RMVar_hsa_circ_330317,RMVar_hsa_circ_272994,RMVar_hsa_circ_289025,RMVar_hsa_circ_113704,RMVar_hsa_circ_216664,RMVar_hsa_circ_216666,RMVar_hsa_circ_216665,RMVar_hsa_circ_216663,RMVar_hsa_circ_267055,RMVar_hsa_circ_269222 102015 RMVar_ID_102015 Human_SNP_ID_128343026 m1A Human chr3 + 32570677 32570677 32570677 GTCGTCGCCTGCCGCGGCGCCACCGTTGCCCGACGCTATCTCGTTGCCCAAGGGGCCGCCAGTGT GTCGTCGCCTGCCGCGGCGCCACCGTTGCCCGGCGCTATCTCGTTGCCCAAGGGGCCGCCAGTGT A G NONHSAG034706.2 RNACentral:URS00008BECA2 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:32570626..32570786 26863196 MeRIP-seq:(Medium) rs148433178 Functional Loss SNV dbSNP153 33..33 33 - - - 102016 RMVar_ID_102016 Human_SNP_ID_128343068 m1A Human chr3 + 32570751 32570751 32570751 ATAATCCCGGCGGAGAAGAACCGAAGGAGCCGACTCGCCCCACGGCCGCCATCTTGGTCGGGAAT ATAATCCCGGCGGAGAAGAACCGAAGGAGCCGTCTCGCCCCACGGCCGCCATCTTGGTCGGGAAT A T NONHSAG034706.2 RNACentral:URS00008BECA2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:32570261..32571141 26863196 MeRIP-seq:(Medium) rs773484606 Functional Loss SNV dbSNP153 33..33 33 - - - 102017 RMVar_ID_102017 Human_SNP_ID_128373786 m1A Human chr3 + 32685416 32685416 32685416 CCAGGACAGCGGCCAGCCCGGCGGCGGGAGTCAGGGCCACGCCACCTGCAGGGAAGAACCCGAGT CCAGGACAGCGGCCAGCCCGGCGGCGGGAGTCGGGGCCACGCCACCTGCAGGGAAGAACCCGAGT A G CNOT10 Ensembl:ENSG00000182973 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:32685224..32685554 26863196 MeRIP-seq:(Medium) rs1007643511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248630,Human_RBP_ID_4757068,Human_RBP_ID_9302743,Human_RBP_ID_18424164 Human_Splice_Rec_405695,Human_Splice_Rec_405729,Human_Splice_Rec_405765,Human_Splice_Rec_405797,Human_Splice_Rec_405805 102018 RMVar_ID_102018 Human_SNP_ID_128385100 m1A Human chr3 + 32727697 32727697 32727697 TAGGTAAAAAATTTTCAGGAAGACCCATGTGTACGTTACTAACCAATAAGAGATATGAGTTGCTG TAGGTAAAAAATTTTCAGGAAGACCCATGTGTGCGTTACTAACCAATAAGAGATATGAGTTGCTG A G CNOT10 Ensembl:ENSG00000182973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11558687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600193,Human_RBP_ID_1385672,Human_RBP_ID_22509456,Human_RBP_ID_23998041 Human_Splice_Rec_405712,Human_Splice_Rec_405746,Human_Splice_Rec_405780,Human_Splice_Rec_405834,Human_Splice_Rec_405874,Human_Splice_Rec_405902,Human_Splice_Rec_405912 GWAS_ID_13406,GWAS_ID_13407 RMVar_hsa_circ_304329,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_326007,RMVar_hsa_circ_272029,RMVar_hsa_circ_14283,RMVar_hsa_circ_216684,RMVar_hsa_circ_216685,RMVar_hsa_circ_216683,RMVar_hsa_circ_372874,RMVar_hsa_circ_216687,RMVar_hsa_circ_304200,RMVar_hsa_circ_309712,RMVar_hsa_circ_289810,RMVar_hsa_circ_8817,RMVar_hsa_circ_216689,RMVar_hsa_circ_216691,RMVar_hsa_circ_216690,RMVar_hsa_circ_216688,RMVar_hsa_circ_46950,RMVar_hsa_circ_312163,RMVar_hsa_circ_354902,RMVar_hsa_circ_65682,RMVar_hsa_circ_33057,RMVar_hsa_circ_43035,RMVar_hsa_circ_377129,RMVar_hsa_circ_39744,RMVar_hsa_circ_312378,RMVar_hsa_circ_216697,RMVar_hsa_circ_17871,RMVar_hsa_circ_216698 102019 RMVar_ID_102019 Human_SNP_ID_128385101 m1A Human chr3 + 32727697 32727697 32727697 TAGGTAAAAAATTTTCAGGAAGACCCATGTGTACGTTACTAACCAATAAGAGATATGAGTTGCTG TAGGTAAAAAATTTTCAGGAAGACCCATGTGTTCGTTACTAACCAATAAGAGATATGAGTTGCTG A T CNOT10 Ensembl:ENSG00000182973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11558687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600193,Human_RBP_ID_1385672,Human_RBP_ID_22509456,Human_RBP_ID_23998041 Human_Splice_Rec_405712,Human_Splice_Rec_405746,Human_Splice_Rec_405780,Human_Splice_Rec_405834,Human_Splice_Rec_405874,Human_Splice_Rec_405902,Human_Splice_Rec_405912 GWAS_ID_13406,GWAS_ID_13407 RMVar_hsa_circ_304329,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_326007,RMVar_hsa_circ_272029,RMVar_hsa_circ_14283,RMVar_hsa_circ_216684,RMVar_hsa_circ_216685,RMVar_hsa_circ_216683,RMVar_hsa_circ_372874,RMVar_hsa_circ_216687,RMVar_hsa_circ_304200,RMVar_hsa_circ_309712,RMVar_hsa_circ_289810,RMVar_hsa_circ_8817,RMVar_hsa_circ_216689,RMVar_hsa_circ_216691,RMVar_hsa_circ_216690,RMVar_hsa_circ_216688,RMVar_hsa_circ_46950,RMVar_hsa_circ_312163,RMVar_hsa_circ_354902,RMVar_hsa_circ_65682,RMVar_hsa_circ_33057,RMVar_hsa_circ_43035,RMVar_hsa_circ_377129,RMVar_hsa_circ_39744,RMVar_hsa_circ_312378,RMVar_hsa_circ_216697,RMVar_hsa_circ_17871,RMVar_hsa_circ_216698 102020 RMVar_ID_102020 Human_SNP_ID_128460810 m1A Human chr3 + 32998698 32998698 32998698 ATAAAGGGAGAAGGAAGAGGAAAGAGGAATGGAAGAAGGGAGGGAGGCAGGAAAGAAACTGTGAC ATAAAGGGAGAAGGAAGAGGAAAGAGGAATGGTAGAAGGGAGGGAGGCAGGAAAGAAACTGTGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:32998676..32998782 26863196 MeRIP-seq:(Medium) rs1237617608 Functional Loss SNV dbSNP153 33..33 33 - - - 102021 RMVar_ID_102021 Human_SNP_ID_128461390 m1A Human chr3 - 33001170 33001168 33001171 GAGGAGAAGAGAAGAAGGAGAAGGAGAAGAGGAGAGGAGAAGAGAAGAGAGAAAGGAAGAACAAG GAGGAGAAGAGAAGAAGGAGAAGGAGAAGAG___AGGAGAAGAGAAGAGAGAAAGGAAGAACAAG TCTC T GLB1 Ensembl:ENSG00000170266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:33000998..33001323 26863196 MeRIP-seq:(Medium) rs925079493 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_25732441 102022 RMVar_ID_102022 Human_SNP_ID_128464470 m1A Human chr3 - 33014259 33014259 33014259 CTCTCAGTTCCAATATCCTCACGGACTGGACGATCTTTCCACTGGACACTGAGGATGCAGTGTGC CTCTCAGTTCCAATATCCTCACGGACTGGACGGTCTTTCCACTGGACACTGAGGATGCAGTGTGC T C GLB1 Ensembl:ENSG00000170266 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:33014210..33021254 32194978 MeRIP-seq:(Medium) rs13073546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8871567,Human_RBP_ID_22768859 Human_Splice_Rec_405982,Human_Splice_Rec_406012,Human_Splice_Rec_406036,Human_Splice_Rec_406048,Human_Splice_Rec_406058 RMVar_hsa_circ_37176,RMVar_hsa_circ_304461,RMVar_hsa_circ_344468,RMVar_hsa_circ_120518,RMVar_hsa_circ_280507,RMVar_hsa_circ_71996,RMVar_hsa_circ_216710,RMVar_hsa_circ_216711,RMVar_hsa_circ_216709 102023 RMVar_ID_102023 Human_SNP_ID_128489685 m1A Human chr3 - 33114273 33114273 33114273 CAAGCGGTGCAGCCGCAGGCTGATCTCCAGGTAGCCCACGCTCTCGGCCCAGTGCTCGCCGCTGT CAAGCGGTGCAGCCGCAGGCTGATCTCCAGGTGGCCCACGCTCTCGGCCCAGTGCTCGCCGCTGT T C lnc-GLB1-2 RNACentral:URS0000D5D201 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:33114222..33114485 26863196 MeRIP-seq:(Medium) rs1171295906 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 102024 RMVar_ID_102024 Human_SNP_ID_128489686 m1A Human chr3 - 33114273 33114273 33114273 CAAGCGGTGCAGCCGCAGGCTGATCTCCAGGTAGCCCACGCTCTCGGCCCAGTGCTCGCCGCTGT CAAGCGGTGCAGCCGCAGGCTGATCTCCAGGTCGCCCACGCTCTCGGCCCAGTGCTCGCCGCTGT T G lnc-GLB1-2 RNACentral:URS0000D5D201 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:33114222..33114485 26863196 MeRIP-seq:(Medium) rs1171295906 Functional Loss SNV dbSNP153 33..33 33 - - - 102025 RMVar_ID_102025 Human_SNP_ID_128489712 m1A Human chr3 + 33114313 33114313 33114313 GATCAGCCTGCGGCTGCACCGCTTGCTGCGCGACAGCGAGGCCTTCTGCCACCGCAACTGCAGCG GATCAGCCTGCGGCTGCACCGCTTGCTGCGCGGCAGCGAGGCCTTCTGCCACCGCAACTGCAGCG A G CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:33114263..33114468 26863196 MeRIP-seq:(Medium) rs1350182235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600321,Human_RBP_ID_4739420,Human_RBP_ID_22768564 RMVar_hsa_circ_120787,RMVar_hsa_circ_216730 102026 RMVar_ID_102026 Human_SNP_ID_128489748 m1A Human chr3 - 33114402 33114399 33114402 GAGGCAGTGCGCGCGGCGCAGCAGGCCCCCGAAGAGGCGCAGCTCGGGATAGCTGGCGAGGCCGG GAGGCAGTGCGCGCGGCGCAGCAGGCCCCCGA___GGCGCAGCTCGGGATAGCTGGCGAGGCCGG CTCT C lnc-GLB1-2 RNACentral:URS0000D5D201 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:33114351..33114475 26863196 MeRIP-seq:(Medium) rs1288328661 Functional Loss DEL dbSNP153 33..35 33 - - - 102027 RMVar_ID_102027 Human_SNP_ID_128489751 m1A Human chr3 - 33114402 33114402 33114402 GAGGCAGTGCGCGCGGCGCAGCAGGCCCCCGAAGAGGCGCAGCTCGGGATAGCTGGCGAGGCCGG GAGGCAGTGCGCGCGGCGCAGCAGGCCCCCGAGGAGGCGCAGCTCGGGATAGCTGGCGAGGCCGG T C lnc-GLB1-2 RNACentral:URS0000D5D201 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:33114351..33114475 26863196 MeRIP-seq:(Medium) rs775914088 Functional Loss SNV dbSNP153 33..33 33 - - - 102028 RMVar_ID_102028 Human_SNP_ID_128489777 m1A Human chr3 + 33114448 33114448 33114448 GCGCCGCGCGCACTGCCTCAAGCGCTGCAAGCAGGGCCTGCCAGCCTTCCGCCAGTCCCAGCCCA GCGCCGCGCGCACTGCCTCAAGCGCTGCAAGCGGGGCCTGCCAGCCTTCCGCCAGTCCCAGCCCA A G CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:33114351..33114550 26863410 MeRIP-seq:(Medium) rs752605909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600326,Human_RBP_ID_4739426,Human_RBP_ID_22768564 Human_miRNA_ID_2380174,Human_miRNA_ID_3023189 RMVar_hsa_circ_120787,RMVar_hsa_circ_216730 102029 RMVar_ID_102029 Human_SNP_ID_128489778 m1A Human chr3 + 33114448 33114448 33114448 GCGCCGCGCGCACTGCCTCAAGCGCTGCAAGCAGGGCCTGCCAGCCTTCCGCCAGTCCCAGCCCA GCGCCGCGCGCACTGCCTCAAGCGCTGCAAGCTGGGCCTGCCAGCCTTCCGCCAGTCCCAGCCCA A T CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:33114351..33114550 26863410 MeRIP-seq:(Medium) rs752605909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600326,Human_RBP_ID_4739426,Human_RBP_ID_22768564 Human_miRNA_ID_2380174,Human_miRNA_ID_3023189 RMVar_hsa_circ_120787,RMVar_hsa_circ_216730 102030 RMVar_ID_102030 Human_SNP_ID_128489842 m1A Human chr3 + 33114546 33114546 33114546 AGCCCTACAAGTTCCTGCAGTTCGCTTACTTCAAGGCAAGTCCGCCTCGCCCCGTCCCAGGCCCC AGCCCTACAAGTTCCTGCAGTTCGCTTACTTCCAGGCAAGTCCGCCTCGCCCCGTCCCAGGCCCC A C CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:33114526..33114550 32194978 MeRIP-seq:(Medium) rs137853942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032965,Human_RBP_ID_18004450,Human_RBP_ID_19116959 GWAS_ID_13408 RMVar_hsa_circ_120787,RMVar_hsa_circ_216730 102031 RMVar_ID_102031 Human_SNP_ID_128489843 m1A Human chr3 + 33114546 33114546 33114546 AGCCCTACAAGTTCCTGCAGTTCGCTTACTTCAAGGCAAGTCCGCCTCGCCCCGTCCCAGGCCCC AGCCCTACAAGTTCCTGCAGTTCGCTTACTTCGAGGCAAGTCCGCCTCGCCCCGTCCCAGGCCCC A G CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:33114526..33114550 32194978 MeRIP-seq:(Medium) rs137853942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1032965,Human_RBP_ID_18004450,Human_RBP_ID_19116959 GWAS_ID_13408 RMVar_hsa_circ_120787,RMVar_hsa_circ_216730 102032 RMVar_ID_102032 Human_SNP_ID_128496833 m1A Human chr3 + 33142944 33142944 33142944 CCACAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCTCTTTCTCACCTTTACACCTGTC CCACAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCTCTTTCTCACCTTTACACCTGTC A G CRTAP Ensembl:ENSG00000170275 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:33142801..33143025 26863410 MeRIP-seq:(Medium) rs1414037282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600363,Human_RBP_ID_17289985,Human_RBP_ID_17519700,Human_RBP_ID_18004462,Human_RBP_ID_18201596,Human_RBP_ID_18209866,Human_RBP_ID_20786491,Human_RBP_ID_27501171 Human_miRNA_ID_1062231,Human_miRNA_ID_2492433 RMVar_hsa_circ_88820,RMVar_hsa_circ_216733 102033 RMVar_ID_102033 Human_SNP_ID_128497033 m1A Human chr3 + 33143865 33143865 33143865 AACTTGCTCTACGTGGTCAGGAAAGAGCAGGGAGACCAAGCAGAGTCGTGGGCAGGGGTAGAATG AACTTGCTCTACGTGGTCAGGAAAGAGCAGGGGGACCAAGCAGAGTCGTGGGCAGGGGTAGAATG A G CRTAP Ensembl:ENSG00000170275 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:33143668..33144050;chr3:33143676..33144706 26863196 MeRIP-seq:(Medium) rs936406780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88820,RMVar_hsa_circ_216733 102034 RMVar_ID_102034 Human_SNP_ID_128569504 m1A Human chr3 + 33439965 33439965 33439965 AGGGCGCGGGTGAAGCCTCCGGAGGGGCGGCGAGTGGTCACCAGCGGCGGCCGGGACGAGAGCTG AGGGCGCGGGTGAAGCCTCCGGAGGGGCGGCGCGTGGTCACCAGCGGCGGCCGGGACGAGAGCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:33439726..33440400;chr3:33439790..33440539;chr3:33439716..33440400 26863196 MeRIP-seq:(Medium) rs1165765142 Functional Loss SNV dbSNP153 33..33 33 - - - 102035 RMVar_ID_102035 Human_SNP_ID_128569597 m1A Human chr3 + 33440205 33440205 33440205 CCCCGGTCGCATCCTCCTCCGGGACCGCTGGGAGGCTGGACCTCGGGCCGCTCCGAGGACCACAC CCCCGGTCGCATCCTCCTCCGGGACCGCTGGGTGGCTGGACCTCGGGCCGCTCCGAGGACCACAC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:33440076..33440246 26863196 MeRIP-seq:(Medium) rs1201571490 Functional Loss SNV dbSNP153 33..33 33 - - - 102036 RMVar_ID_102036 Human_SNP_ID_128569620 m1A Human chr3 + 33440264 33440264 33440264 CCACACGGGGGCAAGCCCTCCGCCCGCCCGTCACCCGCCCCCAAGCCTTGACTCCTTGCCCCCGG CCACACGGGGGCAAGCCCTCCGCCCGCCCGTCCCCCGCCCCCAAGCCTTGACTCCTTGCCCCCGG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:33440166..33440340 26863410 MeRIP-seq:(Medium) rs1405561168 Functional Loss SNV dbSNP153 33..33 33 - - - 102037 RMVar_ID_102037 Human_SNP_ID_128569630 m1A Human chr3 + 33440282 33440282 33440282 TCCGCCCGCCCGTCACCCGCCCCCAAGCCTTGACTCCTTGCCCCCGGCCCGCCCAGGCTCTAGCG TCCGCCCGCCCGTCACCCGCCCCCAAGCCTTGCCTCCTTGCCCCCGGCCCGCCCAGGCTCTAGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr3:33439801..33440489;chr3:33440139..33440340 26863196,26863410 MeRIP-seq:(Medium) rs1284601773 Functional Loss SNV dbSNP153 33..33 33 - - - 102038 RMVar_ID_102038 Human_SNP_ID_128675398 m1A Human chr3 + 33865374 33865374 33865374 GCTGCGCCAGCTCCATCACAAACGCCTGGCTCAGCTCCTCCTCCACAGGCGCAGGGACCACCCTA GCTGCGCCAGCTCCATCACAAACGCCTGGCTCTGCTCCTCCTCCACAGGCGCAGGGACCACCCTA A T PDCD6IP Ensembl:ENSG00000170248 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:33865323..33865498 26863196 MeRIP-seq:(Medium) rs775379507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785456,Human_RBP_ID_932929,Human_RBP_ID_9302159,Human_RBP_ID_18004665,Human_RBP_ID_22455359,Human_RBP_ID_27051579 Human_Splice_Rec_407435,Human_Splice_Rec_407471,Human_Splice_Rec_407531,Human_Splice_Rec_407597 RMVar_hsa_circ_55238,RMVar_hsa_circ_71430 102039 RMVar_ID_102039 Human_SNP_ID_129464135 m1A Human chr3 - 36993579 36993562 36993579 CCGCCGCGATGCGGTTCACCACTGTCTCGTCCAGCCGCCGAATAACCCCTGCCACGAACGACATT CCGCCGCGATGCGGTTCACCACTGTCTCGTCC_________________TGCCACGAACGACATT AGGGGTTATTCGGCGGCT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:36993530..36993680 26863196 MeRIP-seq:(Medium) rs63751892 Functional Loss DEL dbSNP153 33..49 33 - - - Clinvar_Rec_628 102040 RMVar_ID_102040 Human_SNP_ID_129464177 m1A Human chr3 + 36993589 36993589 36993589 GTGGCAGGGGTTATTCGGCGGCTGGACGAGACAGTGGTGAACCGCATCGCGGCGGGGGAAGTTAT GTGGCAGGGGTTATTCGGCGGCTGGACGAGACCGTGGTGAACCGCATCGCGGCGGGGGAAGTTAT A C MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:36993539..36993680 26863196 MeRIP-seq:(Medium) rs369737664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757084,Human_RBP_ID_7190464 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_629 102041 RMVar_ID_102041 Human_SNP_ID_129464178 m1A Human chr3 + 36993589 36993589 36993589 GTGGCAGGGGTTATTCGGCGGCTGGACGAGACAGTGGTGAACCGCATCGCGGCGGGGGAAGTTAT GTGGCAGGGGTTATTCGGCGGCTGGACGAGACGGTGGTGAACCGCATCGCGGCGGGGGAAGTTAT A G MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:36993539..36993680 26863196 MeRIP-seq:(Medium) rs369737664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757084,Human_RBP_ID_7190464 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_629 102042 RMVar_ID_102042 Human_SNP_ID_129464189 m1A Human chr3 + 36993597 36993597 36993597 GGTTATTCGGCGGCTGGACGAGACAGTGGTGAACCGCATCGCGGCGGGGGAAGTTATCCAGCGGC GGTTATTCGGCGGCTGGACGAGACAGTGGTGAGCCGCATCGCGGCGGGGGAAGTTATCCAGCGGC A G MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:36993548..36993661 26863196 MeRIP-seq:(Medium) rs1403203490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757084 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_630 102043 RMVar_ID_102043 Human_SNP_ID_129464190 m1A Human chr3 + 36993597 36993597 36993597 GGTTATTCGGCGGCTGGACGAGACAGTGGTGAACCGCATCGCGGCGGGGGAAGTTATCCAGCGGC GGTTATTCGGCGGCTGGACGAGACAGTGGTGATCCGCATCGCGGCGGGGGAAGTTATCCAGCGGC A T MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:36993548..36993661 26863196 MeRIP-seq:(Medium) rs1403203490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757084 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_630 102044 RMVar_ID_102044 Human_SNP_ID_129464195 m1A Human chr3 + 36993602 36993602 36993602 TTCGGCGGCTGGACGAGACAGTGGTGAACCGCATCGCGGCGGGGGAAGTTATCCAGCGGCCAGCT TTCGGCGGCTGGACGAGACAGTGGTGAACCGCTTCGCGGCGGGGGAAGTTATCCAGCGGCCAGCT A T MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:36993551..36993675 26863196 MeRIP-seq:(Medium) rs63750648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757084 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_631 GWAS_ID_13409 102045 RMVar_ID_102045 Human_SNP_ID_129464232 m1A Human chr3 + 36993631 36993630 36993631 CGCATCGCGGCGGGGGAAGTTATCCAGCGGCCAGCTAATGCTATCAAAGAGATGATTGAGAACTG CGCATCGCGGCGGGGGAAGTTATCCAGCGGCC_GCTAATGCTATCAAAGAGATGATTGAGAACTG CA C MLH1 Ensembl:ENSG00000076242 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:36993530..36993680 32194978 MeRIP-seq:(Medium) rs587779045 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4757084 Human_Splice_Rec_408573,Human_Splice_Rec_408607,Human_Splice_Rec_408635,Human_Splice_Rec_408669,Human_Splice_Rec_408705,Human_Splice_Rec_408719,Human_Splice_Rec_408743,Human_Splice_Rec_408779,Human_Splice_Rec_408841,Human_Splice_Rec_408875,Human_Splice_Rec_408893,Human_Splice_Rec_408905,Human_Splice_Rec_408943,Human_Splice_Rec_408975 Clinvar_Rec_632 102046 RMVar_ID_102046 Human_SNP_ID_129465178 m1A Human chr3 + 36996571 36996571 36996571 TATCATTGCTTGGCTCATATTAAAATATGTACATTAGAGTAGTTGCAGACTGATAAATTATTTTC TATCATTGCTTGGCTCATATTAAAATATGTACCTTAGAGTAGTTGCAGACTGATAAATTATTTTC A C MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:36996568..36996646 26863196 MeRIP-seq:(Medium) rs377111182 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_633 102047 RMVar_ID_102047 Human_SNP_ID_129465179 m1A Human chr3 + 36996571 36996571 36996571 TATCATTGCTTGGCTCATATTAAAATATGTACATTAGAGTAGTTGCAGACTGATAAATTATTTTC TATCATTGCTTGGCTCATATTAAAATATGTACGTTAGAGTAGTTGCAGACTGATAAATTATTTTC A G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:36996568..36996646 26863196 MeRIP-seq:(Medium) rs377111182 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_633 102048 RMVar_ID_102048 Human_SNP_ID_129469796 m1A Human chr3 - 37012024 37012024 37012024 TTGAGGCATTGGGTAGTGTCCTAACATCAGCTACTGTCTCTCCTTGCTGATAAACAAACAGCAGA TTGAGGCATTGGGTAGTGTCCTAACATCAGCTTCTGTCTCTCCTTGCTGATAAACAAACAGCAGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37011827..37012075 32194978 MeRIP-seq:(Medium) rs876659274 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_634,Clinvar_Rec_12239 102049 RMVar_ID_102049 Human_SNP_ID_129469797 m1A Human chr3 - 37012024 37012024 37012024 TTGAGGCATTGGGTAGTGTCCTAACATCAGCTACTGTCTCTCCTTGCTGATAAACAAACAGCAGA TTGAGGCATTGGGTAGTGTCCTAACATCAGCTGCTGTCTCTCCTTGCTGATAAACAAACAGCAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37011827..37012075 32194978 MeRIP-seq:(Medium) rs876659274 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_634,Clinvar_Rec_12239 102050 RMVar_ID_102050 Human_SNP_ID_129472149 m1A Human chr3 + 37020438 37020438 37020438 GCAGCACATCGAGAGCAAGCTCCTGGGCTCCAATTCCTCCAGGATGTACTTCACCCAGGTCAGGG GCAGCACATCGAGAGCAAGCTCCTGGGCTCCAGTTCCTCCAGGATGTACTTCACCCAGGTCAGGG A G MLH1 Ensembl:ENSG00000076242 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37014506..37025649 32194978 MeRIP-seq:(Medium) rs63751467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18004745 Human_Splice_Rec_408591,Human_Splice_Rec_408655,Human_Splice_Rec_408689,Human_Splice_Rec_408739,Human_Splice_Rec_408763,Human_Splice_Rec_408799,Human_Splice_Rec_408859,Human_Splice_Rec_408891,Human_Splice_Rec_408927,Human_Splice_Rec_408963,Human_Splice_Rec_408995,Human_Splice_Rec_409029,Human_Splice_Rec_409067,Human_Splice_Rec_409107,Human_Splice_Rec_409133,Human_Splice_Rec_409201,Human_Splice_Rec_409235,Human_Splice_Rec_409271,Human_Splice_Rec_409333,Human_Splice_Rec_409359,Human_Splice_Rec_409397,Human_Splice_Rec_409413 Human_miRNA_ID_3076805 Clinvar_Rec_635 GWAS_ID_13410 RMVar_hsa_circ_4486,RMVar_hsa_circ_299501,RMVar_hsa_circ_4958,RMVar_hsa_circ_17073,RMVar_hsa_circ_216967,RMVar_hsa_circ_71045,RMVar_hsa_circ_330763,RMVar_hsa_circ_12941,RMVar_hsa_circ_19777,RMVar_hsa_circ_338707,RMVar_hsa_circ_311559,RMVar_hsa_circ_216973,RMVar_hsa_circ_216974,RMVar_hsa_circ_295456,RMVar_hsa_circ_303899,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_216975,RMVar_hsa_circ_216976 102051 RMVar_ID_102051 Human_SNP_ID_129473751 m1A Human chr3 + 37025951 37025950 37025951 GCTGCCAAAAATCAGAGCTTGGAGGGGGATACAACAAAGGGGACTTCAGAAATGTCAGAGAAGAG GCTGCCAAAAATCAGAGCTTGGAGGGGGATAC_ACAAAGGGGACTTCAGAAATGTCAGAGAAGAG CA C MLH1 Ensembl:ENSG00000076242 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37025748..37028823 32194978 MeRIP-seq:(Medium) rs63750071 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5602377,Human_RBP_ID_22092708 Human_Splice_Rec_408593,Human_Splice_Rec_408657,Human_Splice_Rec_408691,Human_Splice_Rec_408765,Human_Splice_Rec_408801,Human_Splice_Rec_408827,Human_Splice_Rec_408861,Human_Splice_Rec_408929,Human_Splice_Rec_408965,Human_Splice_Rec_408997,Human_Splice_Rec_409031,Human_Splice_Rec_409069,Human_Splice_Rec_409109,Human_Splice_Rec_409135,Human_Splice_Rec_409167,Human_Splice_Rec_409203,Human_Splice_Rec_409237,Human_Splice_Rec_409273,Human_Splice_Rec_409335,Human_Splice_Rec_409361,Human_Splice_Rec_409393,Human_Splice_Rec_409399,Human_Splice_Rec_409415,Human_Splice_Rec_409427,Human_Splice_Rec_409431 Clinvar_Rec_636 RMVar_hsa_circ_4486,RMVar_hsa_circ_299501,RMVar_hsa_circ_4958,RMVar_hsa_circ_17073,RMVar_hsa_circ_216967,RMVar_hsa_circ_71045,RMVar_hsa_circ_330763,RMVar_hsa_circ_12941,RMVar_hsa_circ_19777,RMVar_hsa_circ_338707,RMVar_hsa_circ_216974,RMVar_hsa_circ_295456,RMVar_hsa_circ_303899,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_18986,RMVar_hsa_circ_216975,RMVar_hsa_circ_216976,RMVar_hsa_circ_23418,RMVar_hsa_circ_344148 102052 RMVar_ID_102052 Human_SNP_ID_129477169 m1A Human chr3 - 37040274 37040274 37040274 CAGCTGATTTACCTAAGCTTGGTGGTGTTGAGAAGGTATAACTTGGTTTGATGCTGTGCCAAGGC CAGCTGATTTACCTAAGCTTGGTGGTGTTGAGGAGGTATAACTTGGTTTGATGCTGTGCCAAGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37040224..37047584 32194978 MeRIP-seq:(Medium) rs768770694 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_637 102053 RMVar_ID_102053 Human_SNP_ID_129494349 m1A Human chr3 + 37111806 37111806 37111806 ACACCGCTCCTCACTCCCCACTCACACCCTCAACTAGGCACCTAAGGCTCACCTCTCCCCAGAGA ACACCGCTCCTCACTCCCCACTCACACCCTCATCTAGGCACCTAAGGCTCACCTCTCCCCAGAGA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:37111804..37111908 26863196 MeRIP-seq:(Medium) rs1264236898 Functional Loss SNV dbSNP153 33..33 33 - - - 102054 RMVar_ID_102054 Human_SNP_ID_129545099 m1A Human chr3 - 37315547 37315547 37315547 TCCTGTTTCACCCGACTTAATTCCTGTTGAAGACTGATGCGTTCCTCCTCACTTGTTTTTTCGAT TCCTGTTTCACCCGACTTAATTCCTGTTGAAGGCTGATGCGTTCCTCCTCACTTGTTTTTTCGAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:37315401..37315649 26863196 MeRIP-seq:(Medium) rs1169565640 Functional Loss SNV dbSNP153 33..33 33 - - - 102055 RMVar_ID_102055 Human_SNP_ID_129548490 m1A Human chr3 + 37327793 37327793 37327793 GAGCATCAGCAAGAATTGGAAATACTAAAGAAAGAATATGATCAAGAAAGGGAAGAGAAAATCAA GAGCATCAGCAAGAATTGGAAATACTAAAGAAGGAATATGATCAAGAAAGGGAAGAGAAAATCAA A G GOLGA4 Ensembl:ENSG00000144674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:37327742..37327835 26863196 MeRIP-seq:(Medium) rs769012946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2807792,Human_RBP_ID_5390592,Human_RBP_ID_5602397,Human_RBP_ID_24547382 Human_Splice_Rec_409767,Human_Splice_Rec_409851,Human_Splice_Rec_409951,Human_Splice_Rec_409971 Human_miRNA_ID_2192410,Human_miRNA_ID_2206618 RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_265050,RMVar_hsa_circ_352827,RMVar_hsa_circ_269453,RMVar_hsa_circ_75162,RMVar_hsa_circ_55293,RMVar_hsa_circ_53532,RMVar_hsa_circ_357716,RMVar_hsa_circ_362324,RMVar_hsa_circ_354130,RMVar_hsa_circ_124805,RMVar_hsa_circ_66262,RMVar_hsa_circ_217008,RMVar_hsa_circ_9997,RMVar_hsa_circ_46013,RMVar_hsa_circ_55758,RMVar_hsa_circ_367906,RMVar_hsa_circ_350687,RMVar_hsa_circ_318801,RMVar_hsa_circ_67407,RMVar_hsa_circ_73190,RMVar_hsa_circ_313055 102056 RMVar_ID_102056 Human_SNP_ID_129560302 m1A Human chr3 + 37374803 37374803 37374803 ATTCCCATTCCCAAAGGCAGAAATCAGCCAATAGAAAGGGGCTCCAGGCCCCATGCAGGTTAAAA ATTCCCATTCCCAAAGGCAGAAATCAGCCAATGGAAAGGGGCTCCAGGCCCCATGCAGGTTAAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:37374756..37374828 26863196 MeRIP-seq:(Medium) rs1056661404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14804603 102057 RMVar_ID_102057 Human_SNP_ID_129672728 m1A Human chr3 - 37857414 37857414 37857414 CCTAGAGGCGAGGGACAGAACATGCTCTGGAAAGGTCTGCAATGGCTGGGATTTTGGACACTGGT CCTAGAGGCGAGGGACAGAACATGCTCTGGAAGGGTCTGCAATGGCTGGGATTTTGGACACTGGT T C ITGA9-AS1 Ensembl:ENSG00000235257 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:37857400..37857558 26863196 MeRIP-seq:(Medium) rs1483965999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5604338 102058 RMVar_ID_102058 Human_SNP_ID_129673908 m1A Human chr3 - 37861925 37861925 37861925 CGGGAGAGCCGCGCACGGGGAGGCGGAGCGGGAGGCCCGGCGCCGCTGGAAGCGGGAGCGGGCGG CGGGAGAGCCGCGCACGGGGAGGCGGAGCGGGTGGCCCGGCGCCGCTGGAAGCGGGAGCGGGCGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:37861874..37862035 26863196 MeRIP-seq:(Medium) rs1306115147 Functional Loss SNV dbSNP153 33..33 33 - - - 102059 RMVar_ID_102059 Human_SNP_ID_129710860 m1A Human chr3 - 38020337 38020337 38020337 CTGGCTTTGATCCCCAGGCCTACAGGATGATGAGGATCTACAGGCGCTGCTGAAGGGCAGCCAGC CTGGCTTTGATCCCCAGGCCTACAGGATGATGGGGATCTACAGGCGCTGCTGAAGGGCAGCCAGC T C PLCD1 Ensembl:ENSG00000187091 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38020286..38020399 26863196 MeRIP-seq:(Medium) rs1031466319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_410652,Human_Splice_Rec_410674,Human_Splice_Rec_410702,Human_Splice_Rec_410754 102060 RMVar_ID_102060 Human_SNP_ID_129711723 m1A Human chr3 - 38024387 38024387 38024387 GATCCGGAGCCGGAGCCGCTCCAGGGAGCTCTACCTGCAGGAGCGGAGCCTTAAGGTGGCGGCGC GATCCGGAGCCGGAGCCGCTCCAGGGAGCTCTGCCTGCAGGAGCGGAGCCTTAAGGTGGCGGCGC T C PLCD1 Ensembl:ENSG00000187091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38024297..38024502 26863196 MeRIP-seq:(Medium) rs1041787463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757874 Human_Splice_Rec_410673 102061 RMVar_ID_102061 Human_SNP_ID_129711724 m1A Human chr3 - 38024387 38024387 38024387 GATCCGGAGCCGGAGCCGCTCCAGGGAGCTCTACCTGCAGGAGCGGAGCCTTAAGGTGGCGGCGC GATCCGGAGCCGGAGCCGCTCCAGGGAGCTCTCCCTGCAGGAGCGGAGCCTTAAGGTGGCGGCGC T G PLCD1 Ensembl:ENSG00000187091 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38024297..38024502 26863196 MeRIP-seq:(Medium) rs1041787463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757874 Human_Splice_Rec_410673 102062 RMVar_ID_102062 Human_SNP_ID_129741889 m1A Human chr3 - 38136684 38136684 38136684 GGGGTCACTGCGGCTGCTCTTTCTGCTGCAGGACACCACCCCCGACGAGCTTCTCTCGGCAGTCA GGGGTCACTGCGGCTGCTCTTTCTGCTGCAGGGCACCACCCCCGACGAGCTTCTCTCGGCAGTCA T C ACAA1 Ensembl:ENSG00000060971 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:38136601..38136736 26863410 MeRIP-seq:(Medium) rs1198746850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782799,Human_RBP_ID_934945,Human_RBP_ID_5133380,Human_RBP_ID_5390608,Human_RBP_ID_8571722,Human_RBP_ID_8729752,Human_RBP_ID_19115188,Human_RBP_ID_20893484,Human_RBP_ID_22551391 Human_Splice_Rec_410954,Human_Splice_Rec_410955,Human_Splice_Rec_410972,Human_Splice_Rec_410973,Human_Splice_Rec_410990,Human_Splice_Rec_410991,Human_Splice_Rec_411014,Human_Splice_Rec_411015,Human_Splice_Rec_411034,Human_Splice_Rec_411035,Human_Splice_Rec_411082,Human_Splice_Rec_411083,Human_Splice_Rec_411117,Human_Splice_Rec_411134,Human_Splice_Rec_411135,Human_Splice_Rec_411148,Human_Splice_Rec_411149,Human_Splice_Rec_411158,Human_Splice_Rec_411159,Human_Splice_Rec_411174,Human_Splice_Rec_411175,Human_Splice_Rec_411186,Human_Splice_Rec_411187,Human_Splice_Rec_411190,Human_Splice_Rec_411191,Human_Splice_Rec_411196,Human_Splice_Rec_411197 RMVar_hsa_circ_89235,RMVar_hsa_circ_217061,RMVar_hsa_circ_108622,RMVar_hsa_circ_217064,RMVar_hsa_circ_76566,RMVar_hsa_circ_217063 102063 RMVar_ID_102063 Human_SNP_ID_129749688 m1A Human chr3 + 38165629 38165629 38165629 CTGTCGCTGCTGCTGCGGAGGCCGAGGACAGGACGTGGGCTGGGCCGGGCAGTGCCGGACTCGGA CTGTCGCTGCTGCTGCGGAGGCCGAGGACAGGGCGTGGGCTGGGCCGGGCAGTGCCGGACTCGGA A G OXSR1 Ensembl:ENSG00000172939 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:38165501..38183050 26863196 MeRIP-seq:(Medium) rs995542721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757093,Human_RBP_ID_5506268,Human_RBP_ID_5530258,Human_RBP_ID_8210064,Human_RBP_ID_8943471,Human_RBP_ID_9333663,Human_RBP_ID_9434833,Human_RBP_ID_18423943,Human_RBP_ID_18464373,Human_RBP_ID_19009983,Human_RBP_ID_23119965,Human_RBP_ID_23213434,Human_RBP_ID_24000045,Human_RBP_ID_26771054 102064 RMVar_ID_102064 Human_SNP_ID_129798325 m1A Human chr3 - 38365770 38365770 38365770 TCACCCACTATGCCTCCGGAGCTTGCAACCAGACCACCCCCTGCACCCCCCGCATCCTCAGCCTA TCACCCACTATGCCTCCGGAGCTTGCAACCAGGCCACCCCCTGCACCCCCCGCATCCTCAGCCTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38365739..38365849 26863196 MeRIP-seq:(Medium) rs780157030 Functional Loss SNV dbSNP153 33..33 33 - - - 102065 RMVar_ID_102065 Human_SNP_ID_129820305 m1A Human chr3 - 38454530 38454530 38454530 TCGTGCCCCCAAGTTCGGCGAGCCGGGCGCCCACCGCGCCCCCAGCCCACGCCCCCGGAGGTGAG TCGTGCCCCCAAGTTCGGCGAGCCGGGCGCCCCCCGCGCCCCCAGCCCACGCCCCCGGAGGTGAG T G ACVR2B-AS1 Ensembl:ENSG00000229589 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:38454523..38454826 26863196 MeRIP-seq:(Medium) rs941997783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_411641 102066 RMVar_ID_102066 Human_SNP_ID_129820327 m1A Human chr3 - 38454599 38454599 38454599 CGCGTCCCGGCCCCCATCGCAGGGGCGCCTCTAGGAACCAGAATCCCGCAGATGACTGCACAGAC CGCGTCCCGGCCCCCATCGCAGGGGCGCCTCTGGGAACCAGAATCCCGCAGATGACTGCACAGAC T C ACVR2B-AS1 Ensembl:ENSG00000229589 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:38454572..38454771 26863196 MeRIP-seq:(Medium) rs1156768080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_411641 102067 RMVar_ID_102067 Human_SNP_ID_129820384 m1A Human chr3 + 38454778 38454778 38454778 GGCAGGATTGTAGGTGCAGCAGCAGCAGCAGCATGCGGGGAGGGTTGCATGTCCCTCAGAGTCAC GGCAGGATTGTAGGTGCAGCAGCAGCAGCAGCGTGCGGGGAGGGTTGCATGTCCCTCAGAGTCAC A G ACVR2B Ensembl:ENSG00000114739 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38454760..38454853 26863196 MeRIP-seq:(Medium) rs1253675450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266499,Human_RBP_ID_3720749,Human_RBP_ID_5149900,Human_RBP_ID_5325180,Human_RBP_ID_5474717,Human_RBP_ID_8124532,Human_RBP_ID_8236170,Human_RBP_ID_18464376,Human_RBP_ID_18499640,Human_RBP_ID_21986844,Human_RBP_ID_22480761 102068 RMVar_ID_102068 Human_SNP_ID_129831182 m1A Human chr3 - 38496412 38496411 38496412 ACTACAGCCCCAGCCACGAAGCCGCTCAGAAAACGACGGGAACCCCGGAGGCGGGAAGCGATACT ACTACAGCCCCAGCCACGAAGCCGCTCAGAAA_CGACGGGAACCCCGGAGGCGGGAAGCGATACT GT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:38496384..38496473 26863196 MeRIP-seq:(Medium) rs750909137 Functional Loss DEL dbSNP153 33..33 33 - - - 102069 RMVar_ID_102069 Human_SNP_ID_129831191 m1A Human chr3 - 38496426 38496426 38496426 CTCCCGCAGCGCCCACTACAGCCCCAGCCACGAAGCCGCTCAGAAAACGACGGGAACCCCGGAGG CTCCCGCAGCGCCCACTACAGCCCCAGCCACGGAGCCGCTCAGAAAACGACGGGAACCCCGGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:38496381..38496515 26863196 MeRIP-seq:(Medium) rs138226578 Functional Loss SNV dbSNP153 33..33 33 - - - 102070 RMVar_ID_102070 Human_SNP_ID_129831205 m1A Human chr3 + 38496442 38496442 38496442 CGTTTTCTGAGCGGCTTCGTGGCTGGGGCTGTAGTGGGCGCTGCGGGAGCTGGGCTCGCGGCCCT CGTTTTCTGAGCGGCTTCGTGGCTGGGGCTGTGGTGGGCGCTGCGGGAGCTGGGCTCGCGGCCCT A G EXOG Ensembl:ENSG00000157036 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38496393..38496580 26863196 MeRIP-seq:(Medium) rs1490578573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4764956,Human_RBP_ID_19011680,Human_RBP_ID_23026701 Human_Splice_Rec_411699,Human_Splice_Rec_411713,Human_Splice_Rec_411723,Human_Splice_Rec_411729,Human_Splice_Rec_411739,Human_Splice_Rec_411741,Human_Splice_Rec_411753,Human_Splice_Rec_411767,Human_Splice_Rec_411769,Human_Splice_Rec_411777,Human_Splice_Rec_411787,Human_Splice_Rec_411801,Human_Splice_Rec_411817,Human_Splice_Rec_411827,Human_Splice_Rec_411837 102071 RMVar_ID_102071 Human_SNP_ID_129833886 m1A Human chr3 + 38507736 38507736 38507736 AGAAGAGATTAGAGGCAAGGAGATGAGTTAGGACATACAAGCAGTTGGAGTGAGGAATAATAGAG AGAAGAGATTAGAGGCAAGGAGATGAGTTAGGGCATACAAGCAGTTGGAGTGAGGAATAATAGAG A G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38507625..38507781 26863196 MeRIP-seq:(Medium) rs550304142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7192592,Human_RBP_ID_14810314 RMVar_hsa_circ_354584,RMVar_hsa_circ_35690,RMVar_hsa_circ_217104 102072 RMVar_ID_102072 Human_SNP_ID_129840888 m1A Human chr3 + 38538556 38538553 38538556 GCAGCATGGAGGTGGTGGCTGGCCTGGAAGGGAGGAGGACACTGGGTGGCTGGGGTGCCAAGAGA GCAGCATGGAGGTGGTGGCTGGCCTGGAAG___GGAGGACACTGGGTGGCTGGGGTGCCAAGAGA GGGA G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:38538507..38538602 26863196 MeRIP-seq:(Medium) rs1464347799 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_7192793 102073 RMVar_ID_102073 Human_SNP_ID_129966992 m1A Human chr3 + 39052067 39052067 39052067 CATCACCGGCAGAACACAGCAGGGCGGAGGAAAGTGCAGGTATGGAAGCCCGGTTCCTCGGTCTT CATCACCGGCAGAACACAGCAGGGCGGAGGAAGGTGCAGGTATGGAAGCCCGGTTCCTCGGTCTT A G WDR48 Ensembl:ENSG00000114742 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:39052039..39052133 26863196 MeRIP-seq:(Medium) rs1226227162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18423945,Human_RBP_ID_19115214 Human_Splice_Rec_412773,Human_Splice_Rec_412783,Human_Splice_Rec_412817,Human_Splice_Rec_412853,Human_Splice_Rec_412865 102074 RMVar_ID_102074 Human_SNP_ID_129979403 m1A Human chr3 + 39103541 39103541 39103541 GTAGGGCTCCAGGCCCGCCTGCTGGGCTGGGGAGTTCTCCTGCACCTATCCCACAGCAAAGACCA GTAGGGCTCCAGGCCCGCCTGCTGGGCTGGGGCGTTCTCCTGCACCTATCCCACAGCAAAGACCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:39103449..39103601 26863196 MeRIP-seq:(Medium) rs1341252795 Functional Loss SNV dbSNP153 33..33 33 - - - 102075 RMVar_ID_102075 Human_SNP_ID_129980483 m1A Human chr3 - 39107761 39107761 39107761 CAGAGCGGGATTCCCGAGGCAGGGTCGTGGGCACTCTATCGCGGCGGGCGGTTGAAGGCGTTACA CAGAGCGGGATTCCCGAGGCAGGGTCGTGGGCGCTCTATCGCGGCGGGCGGTTGAAGGCGTTACA T C GORASP1 Ensembl:ENSG00000114745 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:39107711..39107828 26863196 MeRIP-seq:(Medium) rs941674198 Functional Loss SNV dbSNP153 33..33 33 - - - 102076 RMVar_ID_102076 Human_SNP_ID_129990866 m1A Human chr3 - 39146702 39146702 39146702 TTCCTATTCCAGGCTGTCTGTCCCCAGACCCCAGAGCACGTCCGGCACCACCATGACTGGGCTGT TTCCTATTCCAGGCTGTCTGTCCCCAGACCCCGGAGCACGTCCGGCACCACCATGACTGGGCTGT T C CSRNP1 Ensembl:ENSG00000144655 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:39145210..39154625 26863196 MeRIP-seq:(Medium) rs916798667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934979 Human_Splice_Rec_413386,Human_Splice_Rec_413394 Human_miRNA_ID_2423404,Human_miRNA_ID_2433064,Human_miRNA_ID_2906545,Human_miRNA_ID_3025379 RMVar_hsa_circ_90057,RMVar_hsa_circ_217122 102077 RMVar_ID_102077 Human_SNP_ID_129992611 m1A Human chr3 + 39153530 39153530 39153530 CCTGCGCCGCGACTCTGTGCGCTCGGCCCGGCAGCCGTCGGTCCAGCCGCCCCTCGCTCTGCGCG CCTGCGCCGCGACTCTGTGCGCTCGGCCCGGCGGCCGTCGGTCCAGCCGCCCCTCGCTCTGCGCG A G AC092053.3,AC092053.4 Ensembl:ENSG00000283849,Ensembl:ENSG00000284669 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:39146481..39153549;chr3:39146555..39153558;chr3:39146530..39154577 26863196 MeRIP-seq:(Medium) rs1408481905 Functional Loss SNV dbSNP153 33..33 33 - - - 102078 RMVar_ID_102078 Human_SNP_ID_129999073 m1A Human chr3 - 39180358 39180358 39180358 TCTCCACCTTCGTTGGCCCCACTCTCCTCCTCACCCACATCACCCTAGTCACACTGTCTTTCTTG TCTCCACCTTCGTTGGCCCCACTCTCCTCCTCGCCCACATCACCCTAGTCACACTGTCTTTCTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:39180307..39180539 26863196 MeRIP-seq:(Medium) rs113777688 Functional Loss SNV dbSNP153 33..33 33 - - - 102079 RMVar_ID_102079 Human_SNP_ID_130053860 m1A Human chr3 + 39406850 39406847 39406850 TCCTGCTCAAATGAAGGGTGAGAAGACTAGTGATGAAAGCCGGTCAGACTGGATCTGTCTCCCGC TCCTGCTCAAATGAAGGGTGAGAAGACTAG___TGAAAGCCGGTCAGACTGGATCTGTCTCCCGC GTGA G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:39406829..39406957 26863196 MeRIP-seq:(Medium) rs1360505594 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1626468,Human_RBP_ID_14812226,Human_RBP_ID_18423947,Human_RBP_ID_19119498 RMVar_hsa_circ_97838,RMVar_hsa_circ_217125 102080 RMVar_ID_102080 Human_SNP_ID_130053862 m1A Human chr3 + 39406850 39406850 39406850 TCCTGCTCAAATGAAGGGTGAGAAGACTAGTGATGAAAGCCGGTCAGACTGGATCTGTCTCCCGC TCCTGCTCAAATGAAGGGTGAGAAGACTAGTGGTGAAAGCCGGTCAGACTGGATCTGTCTCCCGC A G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:39406829..39406957 26863196 MeRIP-seq:(Medium) rs1452796922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1626468,Human_RBP_ID_14812226,Human_RBP_ID_18423947,Human_RBP_ID_19119498 RMVar_hsa_circ_97838,RMVar_hsa_circ_217125 102081 RMVar_ID_102081 Human_SNP_ID_130054161 m1A Human chr3 - 39407604 39407604 39407604 AAGTTACGACGGGAATCTGAAATAAGAGAGCAACCTATTTCTTTTCATTCCATTGAGTTAAGTAG AAGTTACGACGGGAATCTGAAATAAGAGAGCATCCTATTTCTTTTCATTCCATTGAGTTAAGTAG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:39407601..39407725;chr3:39407601..39407675;chr3:39407601..39407650 26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1192174580 Functional Loss SNV dbSNP153 33..33 33 - - - 102082 RMVar_ID_102082 Human_SNP_ID_130054185 m1A Human chr3 - 39407646 39407645 39407646 GCAGGACATCAAGGGCTCCGGACATTGTGAAAATTTCCCTTTAAGTTACGACGGGAATCTGAAAT GCAGGACATCAAGGGCTCCGGACATTGTGAAA_TTTCCCTTTAAGTTACGACGGGAATCTGAAAT AT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:39407601..39407700 32194978 MeRIP-seq:(Medium) rs770761825 Functional Loss DEL dbSNP153 33..33 33 - - - 102083 RMVar_ID_102083 Human_SNP_ID_130054187 m1A Human chr3 - 39407646 39407646 39407646 GCAGGACATCAAGGGCTCCGGACATTGTGAAAATTTCCCTTTAAGTTACGACGGGAATCTGAAAT GCAGGACATCAAGGGCTCCGGACATTGTGAAAGTTTCCCTTTAAGTTACGACGGGAATCTGAAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:39407601..39407700 32194978 MeRIP-seq:(Medium) rs1803893 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 102084 RMVar_ID_102084 Human_SNP_ID_130054541 m1A Human chr3 + 39408665 39408665 39408665 CCTGGGAGAAGCTTCTGCTGGCAGCTCGTGCAATTGTTGCCATTGAAAACCCTGCTGATGTCAGT CCTGGGAGAAGCTTCTGCTGGCAGCTCGTGCAGTTGTTGCCATTGAAAACCCTGCTGATGTCAGT A G RPSA Ensembl:ENSG00000168028 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr3:39408618..39408708;chr3:39408601..39408725 26863196,32194978 MeRIP-seq:(Medium) rs747434456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601351,Human_RBP_ID_1312683,Human_RBP_ID_1626480,Human_RBP_ID_1962274,Human_RBP_ID_3706944,Human_RBP_ID_4764997,Human_RBP_ID_8571945,Human_RBP_ID_9140308,Human_RBP_ID_14812330,Human_RBP_ID_18005203,Human_RBP_ID_18807711,Human_RBP_ID_23135236,Human_RBP_ID_24000936,Human_RBP_ID_27052166,Human_RBP_ID_27317799 Human_Splice_Rec_413540,Human_Splice_Rec_413548,Human_Splice_Rec_413549,Human_Splice_Rec_413560,Human_Splice_Rec_413561,Human_Splice_Rec_413570,Human_Splice_Rec_413571,Human_Splice_Rec_413582,Human_Splice_Rec_413583,Human_Splice_Rec_413585 Human_miRNA_ID_686036,Human_miRNA_ID_888582,Human_miRNA_ID_1065216,Human_miRNA_ID_1076539,Human_miRNA_ID_2274711,Human_miRNA_ID_2400596,Human_miRNA_ID_2494531,Human_miRNA_ID_2500458,Human_miRNA_ID_3108493,Human_miRNA_ID_3109931 RMVar_hsa_circ_81701,RMVar_hsa_circ_87316,RMVar_hsa_circ_97838,RMVar_hsa_circ_217125,RMVar_hsa_circ_118336,RMVar_hsa_circ_217126,RMVar_hsa_circ_217127,RMVar_hsa_circ_217128 102085 RMVar_ID_102085 Human_SNP_ID_130256352 m1A Human chr3 - 40253223 40253223 40253223 GGTAATGCTAGAGGTGATGTTTTTGGTAAACAAGCGGGGTAAGATTTGCTGAATTCCTTTTACTT GGTAATGCTAGAGGTGATGTTTTTGGTAAACAGGCGGGGTAAGATTTGCTGAATTCCTTTTACTT T C EIF1B-AS1 Ensembl:ENSG00000280739 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:40253187..40253344 26863196 MeRIP-seq:(Medium) rs1306570221 Functional Loss SNV dbSNP153 33..33 33 - - - 102086 RMVar_ID_102086 Human_SNP_ID_130256359 m1A Human chr3 + 40253247 40253247 40253247 TACCCCGCTTGTTTACCAAAAACATCACCTCTAGCATTACCAGTATTAGAGTCACTGCCTGCCCA TACCCCGCTTGTTTACCAAAAACATCACCTCTGGCATTACCAGTATTAGAGTCACTGCCTGCCCA A G MYRIP Ensembl:ENSG00000170011 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:40253198..40253489 26863196 MeRIP-seq:(Medium) rs1193860687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158614,Human_RBP_ID_10095336 102087 RMVar_ID_102087 Human_SNP_ID_130256362 m1A Human chr3 + 40253253 40253253 40253253 GCTTGTTTACCAAAAACATCACCTCTAGCATTACCAGTATTAGAGTCACTGCCTGCCCAGTGACA GCTTGTTTACCAAAAACATCACCTCTAGCATTCCCAGTATTAGAGTCACTGCCTGCCCAGTGACA A C MYRIP Ensembl:ENSG00000170011 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:40253203..40253327 26863196 MeRIP-seq:(Medium) rs1268617649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158614 102088 RMVar_ID_102088 Human_SNP_ID_130269180 m1A Human chr3 + 40309820 40309820 40309820 GCTTCCGCCGCCGCCACTCCAGCCTAATCCCAACCCCAGGGCGAAGCGTTTTCTTATTTATTTCC GCTTCCGCCGCCGCCACTCCAGCCTAATCCCACCCCCAGGGCGAAGCGTTTTCTTATTTATTTCC A C EIF1B Ensembl:ENSG00000114784 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr3:40309721..40309890;chr3:40309773..40309878 26863196,32194978 MeRIP-seq:(Medium) rs56308552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3707005,Human_RBP_ID_5425367,Human_RBP_ID_5506300,Human_RBP_ID_17291320,Human_RBP_ID_17404542,Human_RBP_ID_18954257,Human_RBP_ID_22677668 102089 RMVar_ID_102089 Human_SNP_ID_130303818 m1A Human chr3 - 40457377 40457377 40457377 GAGCGGCATGGTCGACGGCCCCGGAGCCCGCAACAGTAAGACTCACCATGTTGGCGGCGTTAGGC GAGCGGCATGGTCGACGGCCCCGGAGCCCGCATCAGTAAGACTCACCATGTTGGCGGCGTTAGGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:40457375..40457512 26863196 MeRIP-seq:(Medium) rs199751366 Functional Loss SNV dbSNP153 33..33 33 - - - 102090 RMVar_ID_102090 Human_SNP_ID_130303819 m1A Human chr3 - 40457377 40457377 40457377 GAGCGGCATGGTCGACGGCCCCGGAGCCCGCAACAGTAAGACTCACCATGTTGGCGGCGTTAGGC GAGCGGCATGGTCGACGGCCCCGGAGCCCGCACCAGTAAGACTCACCATGTTGGCGGCGTTAGGC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:40457375..40457512 26863196 MeRIP-seq:(Medium) rs199751366 Functional Loss SNV dbSNP153 33..33 33 - - - 102091 RMVar_ID_102091 Human_SNP_ID_130304070 m1A Human chr3 - 40457879 40457877 40457879 CCTCCACGAAGCGCCTGAACACCTAAAATTGGAGGAGAAAGGACAGTGAAACTTACTTAGAAATA CCTCCACGAAGCGCCTGAACACCTAAAATTGG__GAGAAAGGACAGTGAAACTTACTTAGAAATA CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:40457876..40457950 26863196 MeRIP-seq:(Medium) rs573605799 Functional Loss DEL dbSNP153 33..34 33 - - - 102092 RMVar_ID_102092 Human_SNP_ID_130304104 m1A Human chr3 + 40457986 40457986 40457986 AATTGGTCGCGATTGTAGATGTTATTGATCAGAACAGGGTAAGTGTCACAACTTTTTACTAAACA AATTGGTCGCGATTGTAGATGTTATTGATCAGTACAGGGTAAGTGTCACAACTTTTTACTAAACA A T RPL14 Ensembl:ENSG00000188846 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:40457876..40458035 26863410 MeRIP-seq:(Medium) rs770765769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835526,Human_RBP_ID_936860,Human_RBP_ID_9334131,Human_RBP_ID_18013245,Human_RBP_ID_19117086,Human_RBP_ID_21898036,Human_RBP_ID_22092713,Human_RBP_ID_23213099 Human_Splice_Rec_414154,Human_Splice_Rec_414155,Human_Splice_Rec_414164,Human_Splice_Rec_414166,Human_Splice_Rec_414167,Human_Splice_Rec_414176,Human_Splice_Rec_414177,Human_Splice_Rec_414186,Human_Splice_Rec_414187,Human_Splice_Rec_414195,Human_Splice_Rec_414203,Human_Splice_Rec_414205 Human_miRNA_ID_1978548,Human_miRNA_ID_1978549 RMVar_hsa_circ_78228,RMVar_hsa_circ_95151,RMVar_hsa_circ_217145,RMVar_hsa_circ_84138,RMVar_hsa_circ_103163,RMVar_hsa_circ_217146,RMVar_hsa_circ_86129,RMVar_hsa_circ_217148,RMVar_hsa_circ_71933,RMVar_hsa_circ_217149,RMVar_hsa_circ_217147 102093 RMVar_ID_102093 Human_SNP_ID_130305509 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG_____________________TACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..52 33 - - - 102094 RMVar_ID_102094 Human_SNP_ID_130305510 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG__________________CAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..49 33 - - - 102095 RMVar_ID_102095 Human_SNP_ID_130305511 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG_______________CAGCAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTGCTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..46 33 - - - 102096 RMVar_ID_102096 Human_SNP_ID_130305512 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG____________CAGCAGCAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTGCTGCTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..43 33 - - - 102097 RMVar_ID_102097 Human_SNP_ID_130305513 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG_________CAGCAGCAGCAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTGCTGCTGCTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..40 33 - - - 102098 RMVar_ID_102098 Human_SNP_ID_130305514 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG______CAGCAGCAGCAGCAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTGCTGCTGCTGCTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..37 33 - - - 102099 RMVar_ID_102099 Human_SNP_ID_130305515 m1A Human chr3 - 40462049 40462029 40462050 ATCTTTTTTGCTGGAACTTTAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGTACCCTTAGTACC ATCTTTTTTGCTGGAACTTTAGCAGCAGCAG___CAGCAGCAGCAGCAGCAGTACCCTTAGTACC ACTGCTGCTGCTGCTGCTGCTG ACTGCTGCTGCTGCTGCTG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:40462026..40462050 26863196 MeRIP-seq:(Medium) rs57354599 Functional Loss DEL dbSNP153 32..34 33 - - - 102100 RMVar_ID_102100 Human_SNP_ID_130305568 m1A Human chr3 + 40462063 40462061 40462064 TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTAAAGTTCCAGCAAAAAAGATCACCGCCGCGAGTA TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT___GTTCCAGCAAAAAAGATCACCGCCGCGAGTA TAAA T RPL14 Ensembl:ENSG00000188846 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:40461926..40462125 26863410 MeRIP-seq:(Medium) rs779092061 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_69432,Human_RBP_ID_601417,Human_RBP_ID_8572018,Human_RBP_ID_9140419,Human_RBP_ID_9393448,Human_RBP_ID_22509516,Human_RBP_ID_22823336,Human_RBP_ID_24001130,Human_RBP_ID_27052215,Human_RBP_ID_27317827 Human_miRNA_ID_2004314,Human_miRNA_ID_2527931,Human_miRNA_ID_2649243,Human_miRNA_ID_2651189 RMVar_hsa_circ_78228,RMVar_hsa_circ_217146,RMVar_hsa_circ_377455,RMVar_hsa_circ_267689,RMVar_hsa_circ_217154,RMVar_hsa_circ_111974,RMVar_hsa_circ_217155 102101 RMVar_ID_102101 Human_SNP_ID_130305570 m1A Human chr3 + 40462063 40462063 40462063 TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTAAAGTTCCAGCAAAAAAGATCACCGCCGCGAGTA TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTACAGTTCCAGCAAAAAAGATCACCGCCGCGAGTA A C RPL14 Ensembl:ENSG00000188846 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:40461926..40462125 26863410 MeRIP-seq:(Medium) rs774792368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69432,Human_RBP_ID_601417,Human_RBP_ID_8572018,Human_RBP_ID_9140419,Human_RBP_ID_9393448,Human_RBP_ID_22509516,Human_RBP_ID_22823336,Human_RBP_ID_24001130,Human_RBP_ID_27052215,Human_RBP_ID_27317827 Human_miRNA_ID_2004314,Human_miRNA_ID_2527931,Human_miRNA_ID_2649243,Human_miRNA_ID_2651189 RMVar_hsa_circ_78228,RMVar_hsa_circ_217146,RMVar_hsa_circ_377455,RMVar_hsa_circ_267689,RMVar_hsa_circ_217154,RMVar_hsa_circ_111974,RMVar_hsa_circ_217155 102102 RMVar_ID_102102 Human_SNP_ID_130305579 m1A Human chr3 + 40462083 40462081 40462084 CTGCTGCTGCTAAAGTTCCAGCAAAAAAGATCACCGCCGCGAGTAAAAAGGCTCCAGCCCAGAAG CTGCTGCTGCTAAAGTTCCAGCAAAAAAGAT___CGCCGCGAGTAAAAAGGCTCCAGCCCAGAAG TCAC T RPL14 Ensembl:ENSG00000188846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:40462026..40462189;chr3:40462026..40462200 26863196 MeRIP-seq:(Medium) rs1340830971 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_601417,Human_RBP_ID_936866,Human_RBP_ID_1626550,Human_RBP_ID_1962311,Human_RBP_ID_3707050,Human_RBP_ID_4741054,Human_RBP_ID_8572018,Human_RBP_ID_9140419,Human_RBP_ID_9393448,Human_RBP_ID_14813223,Human_RBP_ID_18807777,Human_RBP_ID_22280573,Human_RBP_ID_22509516,Human_RBP_ID_22823336,Human_RBP_ID_24001130,Human_RBP_ID_26507662,Human_RBP_ID_27052215,Human_RBP_ID_27317827,Human_RBP_ID_27501489 RMVar_hsa_circ_78228,RMVar_hsa_circ_217146,RMVar_hsa_circ_377455,RMVar_hsa_circ_267689,RMVar_hsa_circ_217154,RMVar_hsa_circ_111974,RMVar_hsa_circ_217155 102103 RMVar_ID_102103 Human_SNP_ID_130305583 m1A Human chr3 + 40462083 40462083 40462083 CTGCTGCTGCTAAAGTTCCAGCAAAAAAGATCACCGCCGCGAGTAAAAAGGCTCCAGCCCAGAAG CTGCTGCTGCTAAAGTTCCAGCAAAAAAGATCGCCGCCGCGAGTAAAAAGGCTCCAGCCCAGAAG A G RPL14 Ensembl:ENSG00000188846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:40462026..40462189;chr3:40462026..40462200 26863196 MeRIP-seq:(Medium) rs1281849082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601417,Human_RBP_ID_936866,Human_RBP_ID_1626550,Human_RBP_ID_1962311,Human_RBP_ID_3707050,Human_RBP_ID_4741054,Human_RBP_ID_8572018,Human_RBP_ID_9140419,Human_RBP_ID_9393448,Human_RBP_ID_14813223,Human_RBP_ID_18807777,Human_RBP_ID_22280573,Human_RBP_ID_22509516,Human_RBP_ID_22823336,Human_RBP_ID_24001130,Human_RBP_ID_26507662,Human_RBP_ID_27052215,Human_RBP_ID_27317827,Human_RBP_ID_27501489 RMVar_hsa_circ_78228,RMVar_hsa_circ_217146,RMVar_hsa_circ_377455,RMVar_hsa_circ_267689,RMVar_hsa_circ_217154,RMVar_hsa_circ_111974,RMVar_hsa_circ_217155 102104 RMVar_ID_102104 Human_SNP_ID_130306690 m1A Human chr3 - 40465315 40465315 40465315 CATGCCCATCACTCCAGATTTACAAACACAAAACCTCCGAACCCCATATAACATTTCTCCTTTGC CATGCCCATCACTCCAGATTTACAAACACAAAGCCTCCGAACCCCATATAACATTTCTCCTTTGC T C lnc-ULK4-6 RNACentral:URS00008B9A6F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:40465097..40465487 26863196 MeRIP-seq:(Medium) rs796440048 Functional Loss SNV dbSNP153 33..33 33 - - - 102105 RMVar_ID_102105 Human_SNP_ID_130321618 m1A Human chr3 + 40525037 40525037 40525037 CAGAGCGTGGGTTTCAGCGAGTTCTACGTGCCAGGTCCGCCCGGTGCCGGCTTCCTCGCTGCCCC CAGAGCGTGGGTTTCAGCGAGTTCTACGTGCCGGGTCCGCCCGGTGCCGGCTTCCTCGCTGCCCC A G ZNF621 Ensembl:ENSG00000172888 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:40524987..40525102 26863196 MeRIP-seq:(Medium) rs1021564654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248530 Human_Splice_Rec_414331,Human_Splice_Rec_414371 RMVar_hsa_circ_217156 102106 RMVar_ID_102106 Human_SNP_ID_130483297 m1A Human chr3 - 41224003 41224003 41224003 TATACTTCAAATACCCTAAAAAAAGTTAATCAAAAGTCATTAGGATTTAAATTTAGCTTGATTAA TATACTTCAAATACCCTAAAAAAAGTTAATCAGAAGTCATTAGGATTTAAATTTAGCTTGATTAA T C lnc-ULK4-1,lnc-ULK4-1:2 RNACentral:URS00009C5AEE,RNACentral:URS00008C1D9A lincRNA,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:41224001..41224251 32194978 MeRIP-seq:(Medium) rs1023412374 Functional Loss SNV dbSNP153 33..33 33 - - - 102107 RMVar_ID_102107 Human_SNP_ID_130485683 m1A Human chr3 + 41233372 41233372 41233372 GGTGGAATGCAAGCTTTAGGACTTCACCTGACAGATCCAAGTCAACGTCTTGTTCAGAACTGTCT GGTGGAATGCAAGCTTTAGGACTTCACCTGACGGATCCAAGTCAACGTCTTGTTCAGAACTGTCT A G CTNNB1 Ensembl:ENSG00000168036 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs754498236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601624,Human_RBP_ID_937071,Human_RBP_ID_1626667,Human_RBP_ID_1962447,Human_RBP_ID_3707240,Human_RBP_ID_3964941,Human_RBP_ID_7194205,Human_RBP_ID_8236014,Human_RBP_ID_8572139,Human_RBP_ID_8871961,Human_RBP_ID_9261110,Human_RBP_ID_14816203,Human_RBP_ID_18807892,Human_RBP_ID_22456555,Human_RBP_ID_22677678,Human_RBP_ID_22768585,Human_RBP_ID_25763623,Human_RBP_ID_26346675 Human_Splice_Rec_414432,Human_Splice_Rec_414433,Human_Splice_Rec_414470,Human_Splice_Rec_414471,Human_Splice_Rec_414502,Human_Splice_Rec_414503,Human_Splice_Rec_414532,Human_Splice_Rec_414533,Human_Splice_Rec_414564,Human_Splice_Rec_414565,Human_Splice_Rec_414594,Human_Splice_Rec_414595,Human_Splice_Rec_414624,Human_Splice_Rec_414625,Human_Splice_Rec_414652,Human_Splice_Rec_414653,Human_Splice_Rec_414684,Human_Splice_Rec_414685,Human_Splice_Rec_414712,Human_Splice_Rec_414713,Human_Splice_Rec_414746,Human_Splice_Rec_414747,Human_Splice_Rec_414776,Human_Splice_Rec_414777,Human_Splice_Rec_414804,Human_Splice_Rec_414805,Human_Splice_Rec_414834,Human_Splice_Rec_414835,Human_Splice_Rec_414864,Human_Splice_Rec_414865,Human_Splice_Rec_414894,Human_Splice_Rec_414895,Human_Splice_Rec_414926,Human_Splice_Rec_414927,Human_Splice_Rec_414956,Human_Splice_Rec_414957,Human_Splice_Rec_414982,Human_Splice_Rec_414983,Human_Splice_Rec_415010,Human_Splice_Rec_415011,Human_Splice_Rec_415040,Human_Splice_Rec_415041,Human_Splice_Rec_415072,Human_Splice_Rec_415073,Human_Splice_Rec_415100,Human_Splice_Rec_415101,Human_Splice_Rec_415130,Human_Splice_Rec_415131,Human_Splice_Rec_415154,Human_Splice_Rec_415155,Human_Splice_Rec_415182,Human_Splice_Rec_415183,Human_Splice_Rec_415214,Human_Splice_Rec_415215,Human_Splice_Rec_415244,Human_Splice_Rec_415245,Human_Splice_Rec_415274,Human_Splice_Rec_415275,Human_Splice_Rec_415304,Human_Splice_Rec_415305,Human_Splice_Rec_415332,Human_Splice_Rec_415333,Human_Splice_Rec_415352,Human_Splice_Rec_415353,Human_Splice_Rec_415382,Human_Splice_Rec_415383,Human_Splice_Rec_415414,Human_Splice_Rec_415415,Human_Splice_Rec_415444,Human_Splice_Rec_415445,Human_Splice_Rec_415474,Human_Splice_Rec_415475,Human_Splice_Rec_415504,Human_Splice_Rec_415505,Human_Splice_Rec_415534,Human_Splice_Rec_415535,Human_Splice_Rec_415562,Human_Splice_Rec_415588,Human_Splice_Rec_415589,Human_Splice_Rec_415616,Human_Splice_Rec_415617,Human_Splice_Rec_415646,Human_Splice_Rec_415647,Human_Splice_Rec_415676,Human_Splice_Rec_415677,Human_Splice_Rec_415704,Human_Splice_Rec_415705,Human_Splice_Rec_415730,Human_Splice_Rec_415731,Human_Splice_Rec_415746,Human_Splice_Rec_415747,Human_Splice_Rec_415757,Human_Splice_Rec_415759 RMVar_hsa_circ_6296,RMVar_hsa_circ_122575,RMVar_hsa_circ_265301,RMVar_hsa_circ_307807,RMVar_hsa_circ_347963,RMVar_hsa_circ_217163,RMVar_hsa_circ_371279,RMVar_hsa_circ_324096,RMVar_hsa_circ_304692,RMVar_hsa_circ_282396,RMVar_hsa_circ_290509,RMVar_hsa_circ_217165,RMVar_hsa_circ_217167,RMVar_hsa_circ_217166,RMVar_hsa_circ_85357,RMVar_hsa_circ_217164,RMVar_hsa_circ_113185,RMVar_hsa_circ_217170,RMVar_hsa_circ_19333,RMVar_hsa_circ_217174,RMVar_hsa_circ_102124,RMVar_hsa_circ_217171,RMVar_hsa_circ_217172,RMVar_hsa_circ_119297,RMVar_hsa_circ_23913,RMVar_hsa_circ_217175,RMVar_hsa_circ_96920,RMVar_hsa_circ_217176,RMVar_hsa_circ_84099,RMVar_hsa_circ_217177,RMVar_hsa_circ_127292,RMVar_hsa_circ_66058,RMVar_hsa_circ_122958,RMVar_hsa_circ_217178,RMVar_hsa_circ_217180,RMVar_hsa_circ_80584,RMVar_hsa_circ_126028,RMVar_hsa_circ_265107,RMVar_hsa_circ_217181,RMVar_hsa_circ_217182 102108 RMVar_ID_102108 Human_SNP_ID_130485789 m1A Human chr3 + 41233757 41233757 41233757 CTGAGCCTGCCATCTGTGCTCTTCGTCATCTGACCAGCCGACACCAAGAAGCAGAGATGGCCCAG CTGAGCCTGCCATCTGTGCTCTTCGTCATCTGCCCAGCCGACACCAAGAAGCAGAGATGGCCCAG A C CTNNB1 Ensembl:ENSG00000168036 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:41233708..41233793 26863196 MeRIP-seq:(Medium) rs1386360637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68668,Human_RBP_ID_783844,Human_RBP_ID_1962453,Human_RBP_ID_8871976,Human_RBP_ID_18005418,Human_RBP_ID_22091593,Human_RBP_ID_22455381,Human_RBP_ID_27052435,Human_RBP_ID_27317947 RMVar_hsa_circ_6296,RMVar_hsa_circ_122575,RMVar_hsa_circ_265301,RMVar_hsa_circ_307807,RMVar_hsa_circ_217163,RMVar_hsa_circ_371279,RMVar_hsa_circ_324096,RMVar_hsa_circ_304692,RMVar_hsa_circ_282396,RMVar_hsa_circ_290509,RMVar_hsa_circ_217165,RMVar_hsa_circ_217167,RMVar_hsa_circ_217166,RMVar_hsa_circ_85357,RMVar_hsa_circ_217164,RMVar_hsa_circ_113185,RMVar_hsa_circ_217170,RMVar_hsa_circ_9987,RMVar_hsa_circ_19333,RMVar_hsa_circ_217174,RMVar_hsa_circ_102124,RMVar_hsa_circ_217171,RMVar_hsa_circ_217172,RMVar_hsa_circ_119297,RMVar_hsa_circ_23913,RMVar_hsa_circ_217175,RMVar_hsa_circ_96920,RMVar_hsa_circ_217176,RMVar_hsa_circ_84099,RMVar_hsa_circ_217177,RMVar_hsa_circ_127292,RMVar_hsa_circ_66058,RMVar_hsa_circ_122958,RMVar_hsa_circ_217178,RMVar_hsa_circ_217180,RMVar_hsa_circ_80584,RMVar_hsa_circ_126028,RMVar_hsa_circ_265107,RMVar_hsa_circ_217181,RMVar_hsa_circ_217182,RMVar_hsa_circ_110217,RMVar_hsa_circ_217183 102109 RMVar_ID_102109 Human_SNP_ID_130485932 m1A Human chr3 + 41234253 41234253 41234253 TAGTTCAGTTGCTTGTTCGTGCACATCAGGATACCCAGCGCCGTACGTCCATGGGTGGGACACAG TAGTTCAGTTGCTTGTTCGTGCACATCAGGATTCCCAGCGCCGTACGTCCATGGGTGGGACACAG A T CTNNB1 Ensembl:ENSG00000168036 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:41234205..41234332 26863196 MeRIP-seq:(Medium) rs758002835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68669,Human_RBP_ID_601633,Human_RBP_ID_1626681,Human_RBP_ID_1962457,Human_RBP_ID_3707246,Human_RBP_ID_3964943,Human_RBP_ID_7194219,Human_RBP_ID_8871986,Human_RBP_ID_9302192,Human_RBP_ID_17704868,Human_RBP_ID_18005422,Human_RBP_ID_18807904,Human_RBP_ID_19115235,Human_RBP_ID_22455384,Human_RBP_ID_22768589,Human_RBP_ID_22823383 Human_Splice_Rec_414437,Human_Splice_Rec_414475,Human_Splice_Rec_414507,Human_Splice_Rec_414537,Human_Splice_Rec_414569,Human_Splice_Rec_414599,Human_Splice_Rec_414629,Human_Splice_Rec_414657,Human_Splice_Rec_414689,Human_Splice_Rec_414717,Human_Splice_Rec_414751,Human_Splice_Rec_414781,Human_Splice_Rec_414809,Human_Splice_Rec_414839,Human_Splice_Rec_414869,Human_Splice_Rec_414899,Human_Splice_Rec_414930,Human_Splice_Rec_414931,Human_Splice_Rec_414961,Human_Splice_Rec_414987,Human_Splice_Rec_415015,Human_Splice_Rec_415045,Human_Splice_Rec_415077,Human_Splice_Rec_415135,Human_Splice_Rec_415159,Human_Splice_Rec_415187,Human_Splice_Rec_415219,Human_Splice_Rec_415249,Human_Splice_Rec_415279,Human_Splice_Rec_415309,Human_Splice_Rec_415357,Human_Splice_Rec_415387,Human_Splice_Rec_415419,Human_Splice_Rec_415449,Human_Splice_Rec_415479,Human_Splice_Rec_415509,Human_Splice_Rec_415539,Human_Splice_Rec_415565,Human_Splice_Rec_415593,Human_Splice_Rec_415621,Human_Splice_Rec_415651,Human_Splice_Rec_415681,Human_Splice_Rec_415709,Human_Splice_Rec_415735,Human_Splice_Rec_415751,Human_Splice_Rec_415763,Human_Splice_Rec_415765,Human_Splice_Rec_415767 RMVar_hsa_circ_6296,RMVar_hsa_circ_122575,RMVar_hsa_circ_265301,RMVar_hsa_circ_307807,RMVar_hsa_circ_217163,RMVar_hsa_circ_371279,RMVar_hsa_circ_324096,RMVar_hsa_circ_304692,RMVar_hsa_circ_282396,RMVar_hsa_circ_290509,RMVar_hsa_circ_217165,RMVar_hsa_circ_217167,RMVar_hsa_circ_217166,RMVar_hsa_circ_85357,RMVar_hsa_circ_217164,RMVar_hsa_circ_113185,RMVar_hsa_circ_217170,RMVar_hsa_circ_19333,RMVar_hsa_circ_217174,RMVar_hsa_circ_102124,RMVar_hsa_circ_217171,RMVar_hsa_circ_217172,RMVar_hsa_circ_119297,RMVar_hsa_circ_217175,RMVar_hsa_circ_96920,RMVar_hsa_circ_217176,RMVar_hsa_circ_84099,RMVar_hsa_circ_217177,RMVar_hsa_circ_127292,RMVar_hsa_circ_122958,RMVar_hsa_circ_217178,RMVar_hsa_circ_217180,RMVar_hsa_circ_80584,RMVar_hsa_circ_126028,RMVar_hsa_circ_265107,RMVar_hsa_circ_217181,RMVar_hsa_circ_217182,RMVar_hsa_circ_110217,RMVar_hsa_circ_118957,RMVar_hsa_circ_217183,RMVar_hsa_circ_309915,RMVar_hsa_circ_217184 102110 RMVar_ID_102110 Human_SNP_ID_130694133 m1A Human chr3 - 42013768 42013768 42013768 GGGGACGCCTCGCTTGAGGCGCGCGGGCGTCAAGGGCTCGGGGCGCGCGGGGGCGGCGGCCGGGT GGGGACGCCTCGCTTGAGGCGCGCGGGCGTCACGGGCTCGGGGCGCGCGGGGGCGGCGGCCGGGT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:42013678..42014025 26863410 MeRIP-seq:(Medium) rs973570091 Functional Loss SNV dbSNP153 33..33 33 - - - 102111 RMVar_ID_102111 Human_SNP_ID_130694196 m1A Human chr3 + 42013957 42013957 42013957 GCGGGCAGCAGGAGGCGGCGGCGCCAGAGCGGAGCCCCCGCGAGTGCCCCCGTGCCGCCCGGCCG GCGGGCAGCAGGAGGCGGCGGCGCCAGAGCGGCGCCCCCGCGAGTGCCCCCGTGCCGCCCGGCCG A C TRAK1 Ensembl:ENSG00000182606 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:42013668..42014117 26863196 MeRIP-seq:(Medium) rs1415998332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248627,Human_RBP_ID_4756402,Human_RBP_ID_22533898 102112 RMVar_ID_102112 Human_SNP_ID_130698354 m1A Human chr3 - 42029912 42029912 42029912 GTGCAAAACCCTCTCTACCATCCGTACTTCCAATCGTGCCTCCCCTATTCTGGCTCTCCACACAG GTGCAAAACCCTCTCTACCATCCGTACTTCCAGTCGTGCCTCCCCTATTCTGGCTCTCCACACAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:42029908..42030056 26863196 MeRIP-seq:(Medium) rs891100498 Functional Loss SNV dbSNP153 33..33 33 - - - 102113 RMVar_ID_102113 Human_SNP_ID_130817221 m1A Human chr3 + 42502731 42502731 42502731 CCGCGCGGGGCCGCCCGCCGCGGGCTCAGGGCAGACCATGCGCCCGCCAAGTCCGCTGCCCGCCC CCGCGCGGGGCCGCCCGCCGCGGGCTCAGGGCCGACCATGCGCCCGCCAAGTCCGCTGCCCGCCC A C VIPR1 Ensembl:ENSG00000114812 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:42502652..42502737 26863410 MeRIP-seq:(Medium) rs1303045358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_416311,Human_Splice_Rec_416327,Human_Splice_Rec_416349,Human_Splice_Rec_416367,Human_Splice_Rec_416389,Human_Splice_Rec_416407,Human_Splice_Rec_416417,Human_Splice_Rec_416441 Human_miRNA_ID_2455006,Human_miRNA_ID_3089891 RMVar_hsa_circ_87600,RMVar_hsa_circ_217232 102114 RMVar_ID_102114 Human_SNP_ID_130836493 m1A Human chr3 - 42581901 42581901 42581901 GGCCGAGCCCTCCCGGTCGGCTAAGATTGCTGAGGAGGCGGCGGGTAGCTGGCAGGCGCCGACTT GGCCGAGCCCTCCCGGTCGGCTAAGATTGCTGGGGAGGCGGCGGGTAGCTGGCAGGCGCCGACTT T C SEC22C Ensembl:ENSG00000093183 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:42581821..42581905 26863196 MeRIP-seq:(Medium) rs1231949979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601867,Human_RBP_ID_4756406,Human_RBP_ID_17404558 Human_Splice_Rec_416769,Human_Splice_Rec_416779,Human_Splice_Rec_416791,Human_Splice_Rec_416815,Human_Splice_Rec_416839,Human_Splice_Rec_416847,Human_Splice_Rec_416863,Human_Splice_Rec_416871,Human_Splice_Rec_416879,Human_Splice_Rec_416887,Human_Splice_Rec_416895 102115 RMVar_ID_102115 Human_SNP_ID_130836519 m1A Human chr3 + 42581935 42581935 42581935 AGCAATCTTAGCCGACCGGGAGGGCTCGGCCCAGGTCACCGGCAGCCCAGGCGCAGGTAGGCCGT AGCAATCTTAGCCGACCGGGAGGGCTCGGCCCTGGTCACCGGCAGCCCAGGCGCAGGTAGGCCGT A T SS18L2 Ensembl:ENSG00000008324 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:42581834..42581965 26863196 MeRIP-seq:(Medium) rs1025524291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_416901 RMVar_hsa_circ_217239 102116 RMVar_ID_102116 Human_SNP_ID_130837507 m1A Human chr3 + 42586249 42586248 42586250 CTTCCTTGTTCTTTTGTTGTTGTTGTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA CTTCCTTGTTCTTTTGTTGTTGTTGTTGAGAC__AGTCTCGCTCTGTCACCCAGGCTGGAGTGCA CAG C SS18L2 Ensembl:ENSG00000008324 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1031591986 Functional Loss DEL dbSNP153 33..34 33 - - - 102117 RMVar_ID_102117 Human_SNP_ID_130841236 m1A Human chr3 - 42600735 42600735 42600735 CCAGCCTGAGCGGGTCCCCGTGAGCAGAAGAGAAAGCACTGCCACTGCAGCCAAACCCCAACGCC CCAGCCTGAGCGGGTCCCCGTGAGCAGAAGAGGAAGCACTGCCACTGCAGCCAAACCCCAACGCC T C SEC22C Ensembl:ENSG00000093183 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:42600685..42600822 26863196 MeRIP-seq:(Medium) rs1293064780 Functional Loss SNV dbSNP153 33..33 33 - - - 102118 RMVar_ID_102118 Human_SNP_ID_130841244 m1A Human chr3 - 42600745 42600745 42600745 TGGCTGGCCTCCAGCCTGAGCGGGTCCCCGTGAGCAGAAGAGAAAGCACTGCCACTGCAGCCAAA TGGCTGGCCTCCAGCCTGAGCGGGTCCCCGTGGGCAGAAGAGAAAGCACTGCCACTGCAGCCAAA T C SEC22C Ensembl:ENSG00000093183 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:42600696..42600786 26863196 MeRIP-seq:(Medium) rs1320652299 Functional Loss SNV dbSNP153 33..33 33 - - - 102119 RMVar_ID_102119 Human_SNP_ID_130850832 m1A Human chr3 + 42638707 42638707 42638707 AAAAAAGTGAAAGAGAAATTGAAAGGGAAAAAAGACAAAAAGCATAAGGCTCCAAAACGAAAGCA AAAAAAGTGAAAGAGAAATTGAAAGGGAAAAAGGACAAAAAGCATAAGGCTCCAAAACGAAAGCA A G NKTR Ensembl:ENSG00000114857 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:42638658..42638752 26863196 MeRIP-seq:(Medium) rs372421485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281378,RMVar_hsa_circ_373281,RMVar_hsa_circ_5244,RMVar_hsa_circ_7711,RMVar_hsa_circ_217248,RMVar_hsa_circ_364420,RMVar_hsa_circ_300989,RMVar_hsa_circ_217254,RMVar_hsa_circ_217252,RMVar_hsa_circ_85895,RMVar_hsa_circ_302073,RMVar_hsa_circ_41173,RMVar_hsa_circ_217253 102120 RMVar_ID_102120 Human_SNP_ID_130855718 m1A Human chr3 + 42658487 42658487 42658487 GTGCTAGCCGCCTACAGCCAGTTCTTCCACTCACTCTTCACCCAGAACAAGCAGCTGCAGCGTGT GTGCTAGCCGCCTACAGCCAGTTCTTCCACTCGCTCTTCACCCAGAACAAGCAGCTGCAGCGTGT A G ZBTB47 Ensembl:ENSG00000114853 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:42658436..42658543 26863196 MeRIP-seq:(Medium) rs988090668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157521,Human_RBP_ID_5425391,Human_RBP_ID_8572478,Human_RBP_ID_22423443 102121 RMVar_ID_102121 Human_SNP_ID_130856068 m1A Human chr3 + 42659300 42659297 42659300 GAGGAAGAGGGTGGCAGTCAGGGAGAAGAGGAAGAAGAGGAGGAGGACGGGCACAGTGAGCAGGA GAGGAAGAGGGTGGCAGTCAGGGAGAAGAG___GAAGAGGAGGAGGACGGGCACAGTGAGCAGGA GGAA G ZBTB47 Ensembl:ENSG00000114853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:42659105..42659643;chr3:42659048..42659668 26863196 MeRIP-seq:(Medium) rs777055793 Functional Loss DEL dbSNP153 31..33 33 - - - 102122 RMVar_ID_102122 Human_SNP_ID_130856387 m1A Human chr3 - 42660064 42660064 42660064 GGCCAAGGGTACTGTTTGTTCCAATCCTCTGCACATCTCTTCATGCGCCCAACTCTATCCACCTC GGCCAAGGGTACTGTTTGTTCCAATCCTCTGCCCATCTCTTCATGCGCCCAACTCTATCCACCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:42660015..42660202 26863196 MeRIP-seq:(Medium) rs1169140718 Functional Loss SNV dbSNP153 33..33 33 - - - 102123 RMVar_ID_102123 Human_SNP_ID_130856523 m1A Human chr3 + 42660652 42660652 42660652 TAGCAGGTAGGTGGGTGCTAATTGCCTGCGCTAATTGCTAATTGCAGTGCCCTGTGGAGAAAGTG TAGCAGGTAGGTGGGTGCTAATTGCCTGCGCTGATTGCTAATTGCAGTGCCCTGTGGAGAAAGTG A G ZBTB47 Ensembl:ENSG00000114853 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:42660636..42660748 32194978 MeRIP-seq:(Medium) rs1015310849 Functional Loss SNV dbSNP153 33..33 33 - - - 102124 RMVar_ID_102124 Human_SNP_ID_130857497 m1A Human chr3 + 42664465 42664465 42664465 CGTCCCCGCTGCCCCAGGCCTGCCCCCAACCCAGCCCCAGGCGCACGCACTGCCCCTGCTCCCGG CGTCCCCGCTGCCCCAGGCCTGCCCCCAACCCCGCCCCAGGCGCACGCACTGCCCCTGCTCCCGG A C ZBTB47 Ensembl:ENSG00000114853 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:42664418..42664603 26863196 MeRIP-seq:(Medium) rs1290796766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1013322 102125 RMVar_ID_102125 Human_SNP_ID_130857768 m1A Human chr3 - 42665189 42665189 42665189 TGGTCTGCAGTCTCCGCACCTCGCCACCCTCCACCCCCCACGCTCACCCAGGTCCAGTCTCAGGC TGGTCTGCAGTCTCCGCACCTCGCCACCCTCCGCCCCCCACGCTCACCCAGGTCCAGTCTCAGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:42665140..42665265 26863196 MeRIP-seq:(Medium) rs866487176 Functional Loss SNV dbSNP153 33..33 33 - - - 102126 RMVar_ID_102126 Human_SNP_ID_130891958 m1A Human chr3 - 42804112 42804112 42804112 TGATGGGGTGGTAATGAGAGACGGGGGCCAGGAGGGTGTTGACTGGGCCCGACGGCGGGGAGCGA TGATGGGGTGGTAATGAGAGACGGGGGCCAGGGGGGTGTTGACTGGGCCCGACGGCGGGGAGCGA T C HIGD1A,AC006059.2,AC099329.1 Ensembl:ENSG00000181061,Ensembl:ENSG00000280571,Ensembl:ENSG00000235288 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:42804071..42804250 26863196 MeRIP-seq:(Medium) rs1396616776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5389978,Human_RBP_ID_5606314,Human_RBP_ID_7196136,Human_RBP_ID_8211073,Human_RBP_ID_9434573 RMVar_hsa_circ_125624,RMVar_hsa_circ_217257 102127 RMVar_ID_102127 Human_SNP_ID_130892086 m1A Human chr3 - 42804452 42804452 42804452 CTGCAGGGATCGGAAGCCGGTTGGGGTGTGAGAGGTTTTCTCGCTCTAGGTAAGCGAAACAAGCC CTGCAGGGATCGGAAGCCGGTTGGGGTGTGAGGGGTTTTCTCGCTCTAGGTAAGCGAAACAAGCC T C HIGD1A,AC006059.2,AC099329.1 Ensembl:ENSG00000181061,Ensembl:ENSG00000280571,Ensembl:ENSG00000235288 Protein coding,Protein coding,lincRNA 5'UTR,5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:42804321..42804500 26863196 MeRIP-seq:(Medium) rs1246763860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246877,Human_RBP_ID_602031,Human_RBP_ID_1633232,Human_RBP_ID_4756407,Human_RBP_ID_5089848,Human_RBP_ID_5654852,Human_RBP_ID_18424407,Human_RBP_ID_19115256,Human_RBP_ID_22457290,Human_RBP_ID_24002756 Human_Splice_Rec_417385,Human_Splice_Rec_417417,Human_Splice_Rec_417445,Human_Splice_Rec_417451,Human_Splice_Rec_417457,Human_Splice_Rec_417461 Human_miRNA_ID_2449728 RMVar_hsa_circ_125624,RMVar_hsa_circ_217257 102128 RMVar_ID_102128 Human_SNP_ID_130955295 m1A Human chr3 - 43079343 43079343 43079343 AGTTTTTCTGGTATCCAGATTTCTGGAAACCGAGTAATCATGTACTGTTTGATTGGGTGGTTCAT AGTTTTTCTGGTATCCAGATTTCTGGAAACCGCGTAATCATGTACTGTTTGATTGGGTGGTTCAT T G POMGNT2 Ensembl:ENSG00000144647 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602055,Human_RBP_ID_22280878,Human_RBP_ID_27318125,Human_RBP_ID_27501664 Human_miRNA_ID_36866,Human_miRNA_ID_1934738 GWAS_ID_13411,GWAS_ID_13412,GWAS_ID_13413,GWAS_ID_13414,GWAS_ID_13415 RMVar_hsa_circ_119767,RMVar_hsa_circ_217260 102129 RMVar_ID_102129 Human_SNP_ID_130955899 m1A Human chr3 - 43080947 43080947 43080947 CGTGGCCCTCATCGCCAACCGCTTCAACCCCGACAACCTCATGCACGTCTTTCATGACGACCTGC CGTGGCCCTCATCGCCAACCGCTTCAACCCCGGCAACCTCATGCACGTCTTTCATGACGACCTGC T C POMGNT2 Ensembl:ENSG00000144647 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43080901..43081050 26863196 MeRIP-seq:(Medium) rs771977831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18808337 RMVar_hsa_circ_119767,RMVar_hsa_circ_217260 102130 RMVar_ID_102130 Human_SNP_ID_130955900 m1A Human chr3 - 43080947 43080947 43080947 CGTGGCCCTCATCGCCAACCGCTTCAACCCCGACAACCTCATGCACGTCTTTCATGACGACCTGC CGTGGCCCTCATCGCCAACCGCTTCAACCCCGCCAACCTCATGCACGTCTTTCATGACGACCTGC T G POMGNT2 Ensembl:ENSG00000144647 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43080901..43081050 26863196 MeRIP-seq:(Medium) rs771977831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18808337 RMVar_hsa_circ_119767,RMVar_hsa_circ_217260 102131 RMVar_ID_102131 Human_SNP_ID_130961420 m1A Human chr3 + 43105958 43105949 43105958 CCCAGCGCCAGCTTCTGGCCCAGGAGGCCCAGAAGGCCCAGGCAGCCAGCACAGGTTTGGCCGCG CCCAGCGCCAGCTTCTGGCCCAGG_________AGGCCCAGGCAGCCAGCACAGGTTTGGCCGCG GAGGCCCAGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43105913..43106004 26863196 MeRIP-seq:(Medium) rs1036908205 Functional Loss DEL dbSNP153 25..33 33 - - - 102132 RMVar_ID_102132 Human_SNP_ID_131021692 m1A Human chr3 + 43347944 43347941 43347944 GCGGCGGCTCGATAAAGATAGCGGGTTCACCTACTCCTGGCACCGACGGGATAGCAGCGAGGGGC GCGGCGGCTCGATAAAGATAGCGGGTTCAC___CTCCTGGCACCGACGGGATAGCAGCGAGGGGC CCTA C SNRK Ensembl:ENSG00000163788 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43347893..43347972 26863196 MeRIP-seq:(Medium) rs770723198 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_602083,Human_RBP_ID_9301766 102133 RMVar_ID_102133 Human_SNP_ID_131076009 m1A Human chr3 + 43580441 43580441 43580441 AGGGCTTCACTGTCATGCAGTGGAAACACCTGAATCACGATGCCAGACGTGAGCAATCTTCTCAC AGGGCTTCACTGTCATGCAGTGGAAACACCTGGATCACGATGCCAGACGTGAGCAATCTTCTCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:43580404..43598663 32194978 MeRIP-seq:(Medium) rs747434303 Functional Loss SNV dbSNP153 33..33 33 - - - 102134 RMVar_ID_102134 Human_SNP_ID_131085832 m1A Human chr3 + 43621978 43621978 43621978 CGAGAGCCGGCGAGAACCGGAGGCCGGGCGAAAGAGTGCTCGGTGCGGGGGGCGGGCCAGGCCAG CGAGAGCCGGCGAGAACCGGAGGCCGGGCGAAGGAGTGCTCGGTGCGGGGGGCGGGCCAGGCCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:43621880..43622007 26863196 MeRIP-seq:(Medium) rs1418328034 Functional Loss SNV dbSNP153 33..33 33 - - - 102135 RMVar_ID_102135 Human_SNP_ID_131102353 m1A Human chr3 - 43690977 43690977 43690977 TCCTCCTCCGCCGCCATAGCCGCCGCCGCGCAAGCGCCGGGACTTATCTCGAAGCCGGCTGACAG TCCTCCTCCGCCGCCATAGCCGCCGCCGCGCATGCGCCGGGACTTATCTCGAAGCCGGCTGACAG T A ANO10 Ensembl:ENSG00000160746 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43690940..43691262 26863196 MeRIP-seq:(Medium) rs1440156590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18500057 102136 RMVar_ID_102136 Human_SNP_ID_131102354 m1A Human chr3 - 43690977 43690977 43690977 TCCTCCTCCGCCGCCATAGCCGCCGCCGCGCAAGCGCCGGGACTTATCTCGAAGCCGGCTGACAG TCCTCCTCCGCCGCCATAGCCGCCGCCGCGCAGGCGCCGGGACTTATCTCGAAGCCGGCTGACAG T C ANO10 Ensembl:ENSG00000160746 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:43690940..43691262 26863196 MeRIP-seq:(Medium) rs1440156590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18500057 102137 RMVar_ID_102137 Human_SNP_ID_131102372 m1A Human chr3 + 43690993 43690993 43690993 AGATAAGTCCCGGCGCTTGCGCGGCGGCGGCTATGGCGGCGGAGGAGGAGGAGGTGGACTCTGCC AGATAAGTCCCGGCGCTTGCGCGGCGGCGGCTGTGGCGGCGGAGGAGGAGGAGGTGGACTCTGCC A G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:43690948..43691081 26863196 MeRIP-seq:(Medium) rs1001974821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757133,Human_RBP_ID_5206058,Human_RBP_ID_5506360,Human_RBP_ID_23115855,Human_RBP_ID_27501788 Human_Splice_Rec_417959,Human_Splice_Rec_417969,Human_Splice_Rec_417971,Human_Splice_Rec_417985,Human_Splice_Rec_417993,Human_Splice_Rec_418003,Human_Splice_Rec_418015,Human_Splice_Rec_418027,Human_Splice_Rec_418041,Human_Splice_Rec_418051 102138 RMVar_ID_102138 Human_SNP_ID_131102414 m1A Human chr3 + 43691034 43691032 43691034 GAGGAGGAGGAGGTGGACTCTGCCGACACCGGAGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GAGGAGGAGGAGGTGGACTCTGCCGACACCG__GAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GGA G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:43690924..43691262 26863196 MeRIP-seq:(Medium) rs387906336 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_602123,Human_RBP_ID_4757134,Human_RBP_ID_23115855 Human_Splice_Rec_417959,Human_Splice_Rec_417969,Human_Splice_Rec_417971,Human_Splice_Rec_417985,Human_Splice_Rec_417993,Human_Splice_Rec_418003,Human_Splice_Rec_418015,Human_Splice_Rec_418027,Human_Splice_Rec_418041,Human_Splice_Rec_418051 Clinvar_Rec_638 102139 RMVar_ID_102139 Human_SNP_ID_131102420 m1A Human chr3 + 43691034 43691034 43691034 GAGGAGGAGGAGGTGGACTCTGCCGACACCGGAGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GAGGAGGAGGAGGTGGACTCTGCCGACACCGGCGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT A C ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:43690924..43691262 26863196 MeRIP-seq:(Medium) rs138695912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602123,Human_RBP_ID_4757134,Human_RBP_ID_23115855 Human_Splice_Rec_417959,Human_Splice_Rec_417969,Human_Splice_Rec_417971,Human_Splice_Rec_417985,Human_Splice_Rec_417993,Human_Splice_Rec_418003,Human_Splice_Rec_418015,Human_Splice_Rec_418027,Human_Splice_Rec_418041,Human_Splice_Rec_418051 102140 RMVar_ID_102140 Human_SNP_ID_131102421 m1A Human chr3 + 43691034 43691034 43691034 GAGGAGGAGGAGGTGGACTCTGCCGACACCGGAGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GAGGAGGAGGAGGTGGACTCTGCCGACACCGGGGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT A G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:43690924..43691262 26863196 MeRIP-seq:(Medium) rs138695912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602123,Human_RBP_ID_4757134,Human_RBP_ID_23115855 Human_Splice_Rec_417959,Human_Splice_Rec_417969,Human_Splice_Rec_417971,Human_Splice_Rec_417985,Human_Splice_Rec_417993,Human_Splice_Rec_418003,Human_Splice_Rec_418015,Human_Splice_Rec_418027,Human_Splice_Rec_418041,Human_Splice_Rec_418051 102141 RMVar_ID_102141 Human_SNP_ID_131104398 m1A Human chr3 + 43699217 43699217 43699217 TCCTGTGCTGCCTTTCTTCTGTGCATGTGACAATTGGTAGTTGAGAAGAGCATGAACTCACCTAT TCCTGTGCTGCCTTTCTTCTGTGCATGTGACAGTTGGTAGTTGAGAAGAGCATGAACTCACCTAT A G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:43699213..43699302 26863196 MeRIP-seq:(Medium) rs760225213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22676224 102142 RMVar_ID_102142 Human_SNP_ID_131104402 m1A Human chr3 + 43699233 43699233 43699233 TTCTGTGCATGTGACAATTGGTAGTTGAGAAGAGCATGAACTCACCTATTTGTTATTTTGTTTTT TTCTGTGCATGTGACAATTGGTAGTTGAGAAGGGCATGAACTCACCTATTTGTTATTTTGTTTTT A G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:43699230..43699321 26863196 MeRIP-seq:(Medium) rs1346131315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22676224 102143 RMVar_ID_102143 Human_SNP_ID_131104425 m1A Human chr3 - 43699307 43699307 43699307 TTCTTTAAGGTGTGATATAGACGTAGGGCACCATGTGGGGAGCCAACCAGTTAGCCATCCTGACC TTCTTTAAGGTGTGATATAGACGTAGGGCACCTTGTGGGGAGCCAACCAGTTAGCCATCCTGACC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:43699216..43699311;chr3:43699220..43699311 26863196 MeRIP-seq:(Medium) rs376238187 Functional Loss SNV dbSNP153 33..33 33 - - - 102144 RMVar_ID_102144 Human_SNP_ID_131254252 m1A Human chr3 + 44338466 44338466 44338466 TGTGCGCAGGCGCCGTAGGGGGAAGGCCTGGCACGCTCCAGCCAACCAGGGCGTCACCTGCAGCT TGTGCGCAGGCGCCGTAGGGGGAAGGCCTGGCGCGCTCCAGCCAACCAGGGCGTCACCTGCAGCT A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:44338457..44338552 26863196 MeRIP-seq:(Medium) rs905904906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 102145 RMVar_ID_102145 Human_SNP_ID_131256396 m1A Human chr3 + 44347069 44347069 44347069 AGGCGGAAGTACCTAACCATGCCTAGGAAGAAAAGGAGTTGTTGTTTTGTAGAAGGGGTTGGGGT AGGCGGAAGTACCTAACCATGCCTAGGAAGAACAGGAGTTGTTGTTTTGTAGAAGGGGTTGGGGT A C TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44347066..44347556 26863196 MeRIP-seq:(Medium) rs1335692234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 102146 RMVar_ID_102146 Human_SNP_ID_131256428 m1A Human chr3 + 44347186 44347186 44347186 AGAATTATGCCGAGATAGGTAACAGATGAGGAAGAAATTTGGGTTTTGGAGGACGACACGAGATA AGAATTATGCCGAGATAGGTAACAGATGAGGACGAAATTTGGGTTTTGGAGGACGACACGAGATA A C TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:44347184..44347298 26863196 MeRIP-seq:(Medium) rs1398780696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 102147 RMVar_ID_102147 Human_SNP_ID_131256889 m1A Human chr3 + 44348991 44348990 44348991 GCTAGTCACAGAACGAAACTGTAAGCTGGACCAGGGGTGAGGAGGGGAGGTGATAGAAGAATTAT GCTAGTCACAGAACGAAACTGTAAGCTGGACC_GGGGTGAGGAGGGGAGGTGATAGAAGAATTAT CA C TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44348982..44349219 26863196 MeRIP-seq:(Medium) rs1244852402 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 102148 RMVar_ID_102148 Human_SNP_ID_131257236 m1A Human chr3 + 44350181 44350180 44350181 GGGGCAGTTTTATAGGATTTGGGTAGGTAGTGAAAAATTACAGTCAAACGGGGTTGTTCTCTTGA GGGGCAGTTTTATAGGATTTGGGTAGGTAGTG_AAAATTACAGTCAAACGGGGTTGTTCTCTTGA GA G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44350179..44350276 26863196 MeRIP-seq:(Medium) rs1328993042 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 102149 RMVar_ID_102149 Human_SNP_ID_131288137 m1A Human chr3 - 44477618 44477618 44477618 GCGGGACGGGCGGCTGCGGTGGCGGCGGGTGGACCGATTGTCGCTCGGCGGCGGGAGTCGGTGAG GCGGGACGGGCGGCTGCGGTGGCGGCGGGTGGGCCGATTGTCGCTCGGCGGCGGGAGTCGGTGAG T C ZNF445 Ensembl:ENSG00000185219 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44458343..44477670 26863196 MeRIP-seq:(Medium) rs1412350685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248649,Human_RBP_ID_4756416,Human_RBP_ID_9333693,Human_RBP_ID_18424474 Human_Splice_Rec_418305,Human_Splice_Rec_418343 102150 RMVar_ID_102150 Human_SNP_ID_131288139 m1A Human chr3 + 44477621 44477621 44477621 ACCGACTCCCGCCGCCGAGCGACAATCGGTCCACCCGCCGCCACCGCAGCCGCCCGTCCCGCGCC ACCGACTCCCGCCGCCGAGCGACAATCGGTCCCCCCGCCGCCACCGCAGCCGCCCGTCCCGCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:44477519..44477650;chr3:44477546..44477628 26863196 MeRIP-seq:(Medium) rs1051592668 Functional Loss SNV dbSNP153 33..33 33 - - - 102151 RMVar_ID_102151 Human_SNP_ID_131288140 m1A Human chr3 + 44477621 44477621 44477621 ACCGACTCCCGCCGCCGAGCGACAATCGGTCCACCCGCCGCCACCGCAGCCGCCCGTCCCGCGCC ACCGACTCCCGCCGCCGAGCGACAATCGGTCCTCCCGCCGCCACCGCAGCCGCCCGTCCCGCGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:44477519..44477650;chr3:44477546..44477628 26863196 MeRIP-seq:(Medium) rs1051592668 Functional Loss SNV dbSNP153 33..33 33 - - - 102152 RMVar_ID_102152 Human_SNP_ID_131292409 m1A Human chr3 - 44496630 44496630 44496630 CAGTCATGTAACCTGGAGGGGTGATTTTGTGCACTGTGGTGTATGTTTCAGACAATGCAGGAGAA CAGTCATGTAACCTGGAGGGGTGATTTTGTGCTCTGTGGTGTATGTTTCAGACAATGCAGGAGAA T A ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:44496581..44496701 26863196 MeRIP-seq:(Medium) rs887554430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14825704 102153 RMVar_ID_102153 Human_SNP_ID_131293584 m1A Human chr3 - 44500626 44500626 44500626 TTGTCTTATTTTTTTTGGCAGCAGGTAGGAACATGATGGAGAGTTCAGAGCTGACTCCGAAGCAG TTGTCTTATTTTTTTTGGCAGCAGGTAGGAACGTGATGGAGAGTTCAGAGCTGACTCCGAAGCAG T C ZNF852 Ensembl:ENSG00000178917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:44500575..44500662 26863196 MeRIP-seq:(Medium) rs749208170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14825757,Human_RBP_ID_25737307 Human_Splice_Rec_418346,Human_Splice_Rec_418354,Human_Splice_Rec_418358 102154 RMVar_ID_102154 Human_SNP_ID_131294030 m1A Human chr3 - 44502649 44502649 44502649 CTTGTCATTCCAGGATACTGTGGCGTATGAGGACCTGTCTGAGGACTATACTCAGAAGAAATGGA CTTGTCATTCCAGGATACTGTGGCGTATGAGGGCCTGTCTGAGGACTATACTCAGAAGAAATGGA T C ZNF852 Ensembl:ENSG00000178917 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:44502598..44502691 26863196 MeRIP-seq:(Medium) rs755058777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784812,Human_RBP_ID_14825807,Human_RBP_ID_18808547,Human_RBP_ID_24003437 Human_Splice_Rec_418352,Human_Splice_Rec_418356 102155 RMVar_ID_102155 Human_SNP_ID_131295909 m1A Human chr3 - 44510575 44510575 44510575 GGGCGGTCGGCTGCGGTGGCGGCGTTTGGATGATTGTCTCTCGGCGGCGGAGTCGGTGAGCGGCC GGGCGGTCGGCTGCGGTGGCGGCGTTTGGATGGTTGTCTCTCGGCGGCGGAGTCGGTGAGCGGCC T C ZNF852 Ensembl:ENSG00000178917 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr3:44510445..44510625;chr3:44510346..44510625 26863196 MeRIP-seq:(Medium) rs1426139071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785483,Human_RBP_ID_4757138,Human_RBP_ID_17150261,Human_RBP_ID_23026348,Human_RBP_ID_27841375 Human_Splice_Rec_418349,Human_Splice_Rec_418355 102156 RMVar_ID_102156 Human_SNP_ID_131351883 m1A Human chr3 - 44749859 44749859 44749859 TTGGGCCCAGGAGTTCAACGCTGCAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGCAAC TTGGGCCCAGGAGTTCAACGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAGCCTGGGCAAC T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1418121809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4742339 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 102157 RMVar_ID_102157 Human_SNP_ID_131351900 m1A Human chr3 - 44749914 44749914 44749914 GTAGCGACACACACCTGTAGTCCCAGCTGCTCAGGAGGCTAAGCAGGAGGATGGCTTGGGCCCAG GTAGCGACACACACCTGTAGTCCCAGCTGCTCGGGAGGCTAAGCAGGAGGATGGCTTGGGCCCAG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1141633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26507927 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 102158 RMVar_ID_102158 Human_SNP_ID_131351936 m1A Human chr3 - 44750062 44750062 44750062 CACCCAGGCCAGACACAATGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCCAAGGTGGGAGA CACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTGGGAAGCCAAGGTGGGAGA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs372844577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4742340 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 102159 RMVar_ID_102159 Human_SNP_ID_131354415 m1A Human chr3 - 44761596 44761596 44761596 GTCTTCTGTCTTTACCCAGAGCTACCATGAGCAAGCGGAACCAGGTATCGTACGTGCGGCCAGCC GTCTTCTGTCTTTACCCAGAGCTACCATGAGCGAGCGGAACCAGGTATCGTACGTGCGGCCAGCC T C KIAA1143 Ensembl:ENSG00000163807 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:44761526..44761599 26863196 MeRIP-seq:(Medium) rs1260249629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602368,Human_RBP_ID_1627281,Human_RBP_ID_4742354,Human_RBP_ID_7197831 RMVar_hsa_circ_106545,RMVar_hsa_circ_217339 102160 RMVar_ID_102160 Human_SNP_ID_131363553 m1A Human chr3 + 44801866 44801865 44801866 AAAATGATTGTGAAATTCCGAGAGGATCAAATAATACGCTTGGAAAAGCTCCACAAGGAATCCCG AAAATGATTGTGAAATTCCGAGAGGATCAAAT_ATACGCTTGGAAAAGCTCCACAAGGAATCCCG TA T KIF15 Ensembl:ENSG00000163808 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:44801818..44801896 32194978 MeRIP-seq:(Medium) rs771081843 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18808685 RMVar_hsa_circ_9699,RMVar_hsa_circ_46351,RMVar_hsa_circ_48926,RMVar_hsa_circ_14090,RMVar_hsa_circ_307769,RMVar_hsa_circ_347351,RMVar_hsa_circ_371038,RMVar_hsa_circ_343781,RMVar_hsa_circ_290463,RMVar_hsa_circ_28220,RMVar_hsa_circ_71015,RMVar_hsa_circ_217349,RMVar_hsa_circ_217350,RMVar_hsa_circ_50389,RMVar_hsa_circ_345912,RMVar_hsa_circ_63874,RMVar_hsa_circ_365553,RMVar_hsa_circ_217353,RMVar_hsa_circ_24851,RMVar_hsa_circ_217354,RMVar_hsa_circ_217352,RMVar_hsa_circ_265609,RMVar_hsa_circ_5700,RMVar_hsa_circ_217356,RMVar_hsa_circ_12101,RMVar_hsa_circ_15150,RMVar_hsa_circ_107224,RMVar_hsa_circ_274573,RMVar_hsa_circ_335610,RMVar_hsa_circ_217358,RMVar_hsa_circ_217359 102161 RMVar_ID_102161 Human_SNP_ID_131377033 m1A Human chr3 - 44858499 44858499 44858499 CCCACCTTAACCCACAAGTATGGGACACCTCCACTCCCTCCCTGGCAACCCATCACACGCGCATT CCCACCTTAACCCACAAGTATGGGACACCTCCCCTCCCTCCCTGGCAACCCATCACACGCGCATT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44858450..44858615 26863196 MeRIP-seq:(Medium) rs1219493702 Functional Loss SNV dbSNP153 33..33 33 - - - 102162 RMVar_ID_102162 Human_SNP_ID_131377948 m1A Human chr3 - 44861945 44861936 44861945 GGGTACGCGGTCGCGGACACGGCGCCGCCCGGAGGCCCCGGCCTCTCGGCCATGTTGCCTGCTGA GGGTACGCGGTCGCGGACACGGCGCCGCCCGG_________CCTCTCGGCCATGTTGCCTGCTGA GCCGGGGCCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:44861906..44862084 26863196 MeRIP-seq:(Medium) rs1418777705 Functional Loss DEL dbSNP153 33..41 33 - - - 102163 RMVar_ID_102163 Human_SNP_ID_131378091 m1A Human chr3 + 44862234 44862234 44862234 CGGGGCTCTTGGGGTGGGGCGGGGGTGGGCGCAGGGCGCCGCCGCACCCTCGCCGGTCTGTCCCG CGGGGCTCTTGGGGTGGGGCGGGGGTGGGCGCGGGGCGCCGCCGCACCCTCGCCGGTCTGTCCCG A G KIF15,TMEM42 Ensembl:ENSG00000163808,Ensembl:ENSG00000169964 Protein coding,Protein coding intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44862226..44862317 26863196 MeRIP-seq:(Medium) rs922651701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247576,Human_RBP_ID_836909,Human_RBP_ID_8209243,Human_RBP_ID_9434575 RMVar_hsa_circ_94173,RMVar_hsa_circ_217368 102164 RMVar_ID_102164 Human_SNP_ID_131378095 m1A Human chr3 + 44862247 44862247 44862247 GTGGGGCGGGGGTGGGCGCAGGGCGCCGCCGCACCCTCGCCGGTCTGTCCCGCCGGGGCCCCGGG GTGGGGCGGGGGTGGGCGCAGGGCGCCGCCGCCCCCTCGCCGGTCTGTCCCGCCGGGGCCCCGGG A C KIF15,TMEM42 Ensembl:ENSG00000163808,Ensembl:ENSG00000169964 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:44862235..44862337 26863196 MeRIP-seq:(Medium) rs930086283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247576,Human_RBP_ID_836909,Human_RBP_ID_8209243,Human_RBP_ID_9434575 RMVar_hsa_circ_94173,RMVar_hsa_circ_217368 102165 RMVar_ID_102165 Human_SNP_ID_131399870 m1A Human chr3 - 44952272 44952272 44952272 TGGGATTCAAGGCACAGTCTGAGGCAGAATTAACCTGGTGGAGTGAATGGGATGTGGGGAAGAGG TGGGATTCAAGGCACAGTCTGAGGCAGAATTAGCCTGGTGGAGTGAATGGGATGTGGGGAAGAGG T C ZDHHC3 Ensembl:ENSG00000163812 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:44952270..44952453 26863196 MeRIP-seq:(Medium) rs79099429 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13416,GWAS_ID_13417,GWAS_ID_13418 RMVar_hsa_circ_292475,RMVar_hsa_circ_217375,RMVar_hsa_circ_11607,RMVar_hsa_circ_337084,RMVar_hsa_circ_217377,RMVar_hsa_circ_217380,RMVar_hsa_circ_376036,RMVar_hsa_circ_217383,RMVar_hsa_circ_274897 102166 RMVar_ID_102166 Human_SNP_ID_131405322 m1A Human chr3 - 44975995 44975995 44975995 CGGGTCCCGGGTTGGGGACTGCAGGGGAAGGCAGCGGCGGCGGCGGCGGGAGCCCCACCGGGGTC CGGGTCCCGGGTTGGGGACTGCAGGGGAAGGCGGCGGCGGCGGCGGCGGGAGCCCCACCGGGGTC T C ZDHHC3 Ensembl:ENSG00000163812 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:44975883..44976088;chr3:44975861..44976094 26863196 MeRIP-seq:(Medium) rs1421182000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_783705,Human_RBP_ID_4756418,Human_RBP_ID_18424475,Human_RBP_ID_26790609 Human_Splice_Rec_418905,Human_Splice_Rec_418917,Human_Splice_Rec_418933,Human_Splice_Rec_418953,Human_Splice_Rec_418973 RMVar_hsa_circ_217385,RMVar_hsa_circ_77519 102167 RMVar_ID_102167 Human_SNP_ID_131405523 m1A Human chr3 + 44976300 44976300 44976300 GCTCGGCAGCATGGCGTCCGTGACGCTGAGCGAGGCGGAGAAGGTGTACATCGTGCATGGCGTCC GCTCGGCAGCATGGCGTCCGTGACGCTGAGCGCGGCGGAGAAGGTGTACATCGTGCATGGCGTCC A C EXOSC7 Ensembl:ENSG00000075914 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:44976251..44976383 26863196 MeRIP-seq:(Medium) rs140839510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248123,Human_RBP_ID_4757142,Human_RBP_ID_19115262 Human_Splice_Rec_419017,Human_Splice_Rec_419031,Human_Splice_Rec_419039,Human_Splice_Rec_419051,Human_Splice_Rec_419067 102168 RMVar_ID_102168 Human_SNP_ID_131405524 m1A Human chr3 + 44976300 44976300 44976300 GCTCGGCAGCATGGCGTCCGTGACGCTGAGCGAGGCGGAGAAGGTGTACATCGTGCATGGCGTCC GCTCGGCAGCATGGCGTCCGTGACGCTGAGCGGGGCGGAGAAGGTGTACATCGTGCATGGCGTCC A G EXOSC7 Ensembl:ENSG00000075914 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:44976251..44976383 26863196 MeRIP-seq:(Medium) rs140839510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248123,Human_RBP_ID_4757142,Human_RBP_ID_19115262 Human_Splice_Rec_419017,Human_Splice_Rec_419031,Human_Splice_Rec_419039,Human_Splice_Rec_419051,Human_Splice_Rec_419067 102169 RMVar_ID_102169 Human_SNP_ID_131405534 m1A Human chr3 - 44976314 44976314 44976314 TGCTGTAGCTACCTGGACGCCATGCACGATGTACACCTTCTCCGCCTCGCTCAGCGTCACGGACG TGCTGTAGCTACCTGGACGCCATGCACGATGTTCACCTTCTCCGCCTCGCTCAGCGTCACGGACG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:44976251..44976369;chr3:44976251..44976387 26863196 MeRIP-seq:(Medium) rs757102199 Functional Loss SNV dbSNP153 33..33 33 - - - 102170 RMVar_ID_102170 Human_SNP_ID_131405535 m1A Human chr3 - 44976314 44976314 44976314 TGCTGTAGCTACCTGGACGCCATGCACGATGTACACCTTCTCCGCCTCGCTCAGCGTCACGGACG TGCTGTAGCTACCTGGACGCCATGCACGATGTGCACCTTCTCCGCCTCGCTCAGCGTCACGGACG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:44976251..44976369;chr3:44976251..44976387 26863196 MeRIP-seq:(Medium) rs757102199 Functional Loss SNV dbSNP153 33..33 33 - - - 102171 RMVar_ID_102171 Human_SNP_ID_131405988 m1A Human chr3 + 44978076 44978073 44978077 GTTGTGAAATAAATGAAAGATAGGAGGGAGACAAACAGAGAGTAAAAGTGAATAAAATAAAAACA GTTGTGAAATAAATGAAAGATAGGAGGGAG____ACAGAGAGTAAAAGTGAATAAAATAAAAACA GACAA G EXOSC7 Ensembl:ENSG00000075914 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:44978074..44978180 26863196 MeRIP-seq:(Medium) rs1442746257 Functional Loss DEL dbSNP153 31..34 33 - - - 102172 RMVar_ID_102172 Human_SNP_ID_131408449 m1A Human chr3 + 44989201 44989201 44989201 TGAGGACTACCGATGTGTCGAAGTGGAAACTGATGTGGTGTCCAACACTAGTGGGTCCGCCAGGG TGAGGACTACCGATGTGTCGAAGTGGAAACTGGTGTGGTGTCCAACACTAGTGGGTCCGCCAGGG A G EXOSC7 Ensembl:ENSG00000075914 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:44989151..44989200 32194978 MeRIP-seq:(Medium) rs986274804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1963229,Human_RBP_ID_4757144,Human_RBP_ID_18808777,Human_RBP_ID_23213449,Human_RBP_ID_24003932 Human_Splice_Rec_418990,Human_Splice_Rec_418991,Human_Splice_Rec_419006,Human_Splice_Rec_419008,Human_Splice_Rec_419009,Human_Splice_Rec_419018,Human_Splice_Rec_419019,Human_Splice_Rec_419032,Human_Splice_Rec_419033,Human_Splice_Rec_419052,Human_Splice_Rec_419053,Human_Splice_Rec_419072 RMVar_hsa_circ_54479,RMVar_hsa_circ_291137,RMVar_hsa_circ_325872,RMVar_hsa_circ_368299,RMVar_hsa_circ_325153,RMVar_hsa_circ_126708,RMVar_hsa_circ_281416,RMVar_hsa_circ_94539,RMVar_hsa_circ_217386,RMVar_hsa_circ_217388,RMVar_hsa_circ_217390,RMVar_hsa_circ_217391,RMVar_hsa_circ_217389,RMVar_hsa_circ_217387 102173 RMVar_ID_102173 Human_SNP_ID_131408450 m1A Human chr3 + 44989201 44989201 44989201 TGAGGACTACCGATGTGTCGAAGTGGAAACTGATGTGGTGTCCAACACTAGTGGGTCCGCCAGGG TGAGGACTACCGATGTGTCGAAGTGGAAACTGTTGTGGTGTCCAACACTAGTGGGTCCGCCAGGG A T EXOSC7 Ensembl:ENSG00000075914 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:44989151..44989200 32194978 MeRIP-seq:(Medium) rs986274804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1963229,Human_RBP_ID_4757144,Human_RBP_ID_18808777,Human_RBP_ID_23213449,Human_RBP_ID_24003932 Human_Splice_Rec_418990,Human_Splice_Rec_418991,Human_Splice_Rec_419006,Human_Splice_Rec_419008,Human_Splice_Rec_419009,Human_Splice_Rec_419018,Human_Splice_Rec_419019,Human_Splice_Rec_419032,Human_Splice_Rec_419033,Human_Splice_Rec_419052,Human_Splice_Rec_419053,Human_Splice_Rec_419072 RMVar_hsa_circ_54479,RMVar_hsa_circ_291137,RMVar_hsa_circ_325872,RMVar_hsa_circ_368299,RMVar_hsa_circ_325153,RMVar_hsa_circ_126708,RMVar_hsa_circ_281416,RMVar_hsa_circ_94539,RMVar_hsa_circ_217386,RMVar_hsa_circ_217388,RMVar_hsa_circ_217390,RMVar_hsa_circ_217391,RMVar_hsa_circ_217389,RMVar_hsa_circ_217387 102174 RMVar_ID_102174 Human_SNP_ID_186289003 m1A Human chr4 + 61200370 61200370 61200370 GCTCCGGCCCCGGCTGCGCCTACCCCGCGCGCAGGCTGCACGGTCCCCGCGCGCCCGCGCTCTGA GCTCCGGCCCCGGCTGCGCCTACCCCGCGCGCCGGCTGCACGGTCCCCGCGCGCCCGCGCTCTGA A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:61200340..61200430 26863410 MeRIP-seq:(Medium) rs1271581229 Functional Loss SNV dbSNP153 33..33 33 - - - 102175 RMVar_ID_102175 Human_SNP_ID_188031324 m1A Human chr4 + 67502853 67502853 67502853 CTCTTTTTCTTATACACCACGTATCGTCCATCAGAAAATCCTGTTGACTTTACCCTCAAAAATAC CTCTTTTTCTTATACACCACGTATCGTCCATCGGAAAATCCTGTTGACTTTACCCTCAAAAATAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:67502832..67502943 26863196 MeRIP-seq:(Medium) rs558127834 Functional Loss SNV dbSNP153 33..33 33 - - - 102176 RMVar_ID_102176 Human_SNP_ID_188033585 m1A Human chr4 - 67512510 67512510 67512510 ATAAGGAAGAATCTAAAAAGAAGCGCTTTTCCAGTGAGTCCAAGAACAAACTTGTACCTGAAGAA ATAAGGAAGAATCTAAAAAGAAGCGCTTTTCCGGTGAGTCCAAGAACAAACTTGTACCTGAAGAA T C CENPC Ensembl:ENSG00000145241 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:67512377..67512512 26863196 MeRIP-seq:(Medium) rs374698756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_940780,Human_RBP_ID_9396335,Human_RBP_ID_24547672,Human_RBP_ID_26349308,Human_RBP_ID_27824833 Human_Splice_Rec_565408,Human_Splice_Rec_565436,Human_Splice_Rec_565472,Human_Splice_Rec_565520,Human_Splice_Rec_565536 RMVar_hsa_circ_377696,RMVar_hsa_circ_67913,RMVar_hsa_circ_323635,RMVar_hsa_circ_226376,RMVar_hsa_circ_226379,RMVar_hsa_circ_352618,RMVar_hsa_circ_309766,RMVar_hsa_circ_267272,RMVar_hsa_circ_377441,RMVar_hsa_circ_360475 102177 RMVar_ID_102177 Human_SNP_ID_188079732 m1A Human chr4 + 67701102 67701102 67701102 CAGGACGCCTCTTCCCCCTGATGGGCGGCCACAGGCTCGGATCCTTCCATTGCCGCCTGAGACAC CAGGACGCCTCTTCCCCCTGATGGGCGGCCACGGGCTCGGATCCTTCCATTGCCGCCTGAGACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:67700902..67701104 26863196 MeRIP-seq:(Medium) rs1337389237 Functional Loss SNV dbSNP153 33..33 33 - - - 102178 RMVar_ID_102178 Human_SNP_ID_188079733 m1A Human chr4 + 67701102 67701102 67701102 CAGGACGCCTCTTCCCCCTGATGGGCGGCCACAGGCTCGGATCCTTCCATTGCCGCCTGAGACAC CAGGACGCCTCTTCCCCCTGATGGGCGGCCACTGGCTCGGATCCTTCCATTGCCGCCTGAGACAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:67700902..67701104 26863196 MeRIP-seq:(Medium) rs1337389237 Functional Loss SNV dbSNP153 33..33 33 - - - 102179 RMVar_ID_102179 Human_SNP_ID_188232098 m1A Human chr4 - 68329174 68329174 68329174 GGGAGCTACCTTTTTTTATGAAGGAGATGGTTAGGAAAAGAGAAGAACAGAGGGCAAAGATGGAT GGGAGCTACCTTTTTTTATGAAGGAGATGGTTGGGAAAAGAGAAGAACAGAGGGCAAAGATGGAT T C YTHDC1 Ensembl:ENSG00000083896 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:68329171..68329300 26863196 MeRIP-seq:(Medium) rs563687529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10153040,Human_RBP_ID_15187709 RMVar_hsa_circ_55246,RMVar_hsa_circ_226445,RMVar_hsa_circ_369553 102180 RMVar_ID_102180 Human_SNP_ID_188237734 m1A Human chr4 - 68349767 68349767 68349767 TCTAAGCGGCGGCGGCGGTGGCAGCGGCGGAAACCGAAGGGGAGCCATGGCGGCTGACAGTCGGG TCTAAGCGGCGGCGGCGGTGGCAGCGGCGGAAGCCGAAGGGGAGCCATGGCGGCTGACAGTCGGG T C YTHDC1 Ensembl:ENSG00000083896 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:68338308..68350043 26863196 MeRIP-seq:(Medium) rs1324649677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249303,Human_RBP_ID_837374,Human_RBP_ID_18028632,Human_RBP_ID_23034860,Human_RBP_ID_27824851 Human_Splice_Rec_566069,Human_Splice_Rec_566101,Human_Splice_Rec_566131,Human_Splice_Rec_566173 102181 RMVar_ID_102181 Human_SNP_ID_188237738 m1A Human chr4 - 68349777 68349777 68349777 GCGAGTCGCGTCTAAGCGGCGGCGGCGGTGGCAGCGGCGGAAACCGAAGGGGAGCCATGGCGGCT GCGAGTCGCGTCTAAGCGGCGGCGGCGGTGGCGGCGGCGGAAACCGAAGGGGAGCCATGGCGGCT T C YTHDC1 Ensembl:ENSG00000083896 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:68349715..68349875;chr4:68349726..68349925 26863196 MeRIP-seq:(Medium) rs1317950449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249303,Human_RBP_ID_18028632,Human_RBP_ID_23034860 Human_Splice_Rec_566069,Human_Splice_Rec_566101,Human_Splice_Rec_566131,Human_Splice_Rec_566173 102182 RMVar_ID_102182 Human_SNP_ID_188237766 m1A Human chr4 + 68349804 68349804 68349804 GCCGCTGCCACCGCCGCCGCCGCTTAGACGCGACTCGCGCGGGCGCCGCAGCCGCGGCAGAAGCA GCCGCTGCCACCGCCGCCGCCGCTTAGACGCGCCTCGCGCGGGCGCCGCAGCCGCGGCAGAAGCA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:68349739..68349989 32194978 MeRIP-seq:(Medium) rs1216223538 Functional Loss SNV dbSNP153 33..33 33 - - - 102183 RMVar_ID_102183 Human_SNP_ID_188237800 m1A Human chr4 - 68349896 68349892 68349896 AAGGGAAAAAGCGGGAAGAGTCGAGAAGGCTGAGTGTTAAGAGGCCAAGTGCGACGCGCGTATCC AAGGGAAAAAGCGGGAAGAGTCGAGAAGGCTG____TTAAGAGGCCAAGTGCGACGCGCGTATCC ACACT A YTHDC1 Ensembl:ENSG00000083896 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:68349797..68349912 26863196 MeRIP-seq:(Medium) rs900531318 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_623287,Human_RBP_ID_4800233,Human_RBP_ID_15188162,Human_RBP_ID_18825903,Human_RBP_ID_24062164 102184 RMVar_ID_102184 Human_SNP_ID_188237802 m1A Human chr4 - 68349896 68349896 68349896 AAGGGAAAAAGCGGGAAGAGTCGAGAAGGCTGAGTGTTAAGAGGCCAAGTGCGACGCGCGTATCC AAGGGAAAAAGCGGGAAGAGTCGAGAAGGCTGCGTGTTAAGAGGCCAAGTGCGACGCGCGTATCC T G YTHDC1 Ensembl:ENSG00000083896 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:68349797..68349912 26863196 MeRIP-seq:(Medium) rs1258403322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623287,Human_RBP_ID_4800233,Human_RBP_ID_15188162,Human_RBP_ID_18825903,Human_RBP_ID_24062164 102185 RMVar_ID_102185 Human_SNP_ID_188871350 m1A Human chr4 - 70688565 70688565 70688565 ACTCGTGGCTCTAAACAGCAGCGCGCTCCCCTACCACCGGAGTTTGCAGACTCCTGATCGGCTAC ACTCGTGGCTCTAAACAGCAGCGCGCTCCCCTGCCACCGGAGTTTGCAGACTCCTGATCGGCTAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:70688548..70688678 26863196 MeRIP-seq:(Medium) rs924154306 Functional Loss SNV dbSNP153 33..33 33 - - - 102186 RMVar_ID_102186 Human_SNP_ID_188875658 m1A Human chr4 + 70704776 70704776 70704776 GCTTGGACCCTGGCGGGGCGGGCTGTGGGCCGAGCGGCGGAGCCCAGGCGCCAGCCCGTGGCCGA GCTTGGACCCTGGCGGGGCGGGCTGTGGGCCGCGCGGCGGAGCCCAGGCGCCAGCCCGTGGCCGA A C RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr4:70704675..70704800 26863410 MeRIP-seq:(Medium) rs1323512127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18424764 102187 RMVar_ID_102187 Human_SNP_ID_188875680 m1A Human chr4 - 70704818 70704818 70704818 GTCCCGTCCGCTGCGCCGCCGCCGCCACCGCCACCTTTCTTCTCGGCCACGGGCTGGCGCCTGGG GTCCCGTCCGCTGCGCCGCCGCCGCCACCGCCCCCTTTCTTCTCGGCCACGGGCTGGCGCCTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:70704741..70705117 26863196 MeRIP-seq:(Medium) rs895883800 Functional Loss SNV dbSNP153 33..33 33 - - - 102188 RMVar_ID_102188 Human_SNP_ID_188875731 m1A Human chr4 + 70704946 70704946 70704946 CTGCGGCGAAGGAAGGAGTGAGCATGGCTGAGACCCCGCCGCCGCCCACCGCTGGTGCCGAAAGT CTGCGGCGAAGGAAGGAGTGAGCATGGCTGAGCCCCCGCCGCCGCCCACCGCTGGTGCCGAAAGT A C RUFY3 Ensembl:ENSG00000018189 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:70704699..70705048 26863196 MeRIP-seq:(Medium) rs1041759319 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19013750 Human_Splice_Rec_567296 102189 RMVar_ID_102189 Human_SNP_ID_188907889 m1A Human chr4 - 70833168 70833168 70833168 CTTAATTGAAATGGAGTCAGAGCAGGATGTGCAGAAAGCCTTAGAGAAGCACCGCATGTACATGG CTTAATTGAAATGGAGTCAGAGCAGGATGTGCGGAAAGCCTTAGAGAAGCACCGCATGTACATGG T C GRSF1 Ensembl:ENSG00000132463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:70833084..70833235 26863196 MeRIP-seq:(Medium) rs1203510506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942101,Human_RBP_ID_1980471,Human_RBP_ID_4789458,Human_RBP_ID_7323857,Human_RBP_ID_15191034,Human_RBP_ID_24062837 Human_Splice_Rec_567489,Human_Splice_Rec_567507,Human_Splice_Rec_567523,Human_Splice_Rec_567541,Human_Splice_Rec_567559,Human_Splice_Rec_567577,Human_Splice_Rec_567591 Human_miRNA_ID_3116498 RMVar_hsa_circ_292100,RMVar_hsa_circ_368019,RMVar_hsa_circ_61424,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224,RMVar_hsa_circ_226471,RMVar_hsa_circ_274787,RMVar_hsa_circ_80140,RMVar_hsa_circ_28328,RMVar_hsa_circ_55954,RMVar_hsa_circ_226472 102190 RMVar_ID_102190 Human_SNP_ID_188908806 m1A Human chr4 + 70836197 70836197 70836197 AAAGTTAAGCACATCTTCCATAGTGCATGACCAGGGCAGTCCTTGAGCTCGAATGAGAAAGACAT AAAGTTAAGCACATCTTCCATAGTGCATGACCGGGGCAGTCCTTGAGCTCGAATGAGAAAGACAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:70836151..70836200 32194978 MeRIP-seq:(Medium) rs1368857182 Functional Loss SNV dbSNP153 33..33 33 - - - 102191 RMVar_ID_102191 Human_SNP_ID_188910128 m1A Human chr4 + 70839720 70839720 70839720 CGGCGGCCCGAGACGCCCGACGGGATAGAGCCAGCGGCGGAGTAGAAGGGCAGGCAGGCGGCGCC CGGCGGCCCGAGACGCCCGACGGGATAGAGCCGGCGGCGGAGTAGAAGGGCAGGCAGGCGGCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:70839676..70839875 26863196 MeRIP-seq:(Medium) rs1374040666 Functional Loss SNV dbSNP153 33..33 33 - - - 102192 RMVar_ID_102192 Human_SNP_ID_188910179 m1A Human chr4 + 70839830 70839830 70839830 CGCCCCGAGTACCCAGCGCGTGCCGGCCATGGACTCCGGAGGCGGCGCAGGGCCTGAAGGCAGCT CGCCCCGAGTACCCAGCGCGTGCCGGCCATGGGCTCCGGAGGCGGCGCAGGGCCTGAAGGCAGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:70839445..70839900;chr4:70839701..70839875 26863196 MeRIP-seq:(Medium) rs1473206255 Functional Loss SNV dbSNP153 33..33 33 - - - 102193 RMVar_ID_102193 Human_SNP_ID_188925739 m1A Human chr4 - 70902394 70902394 70902394 AGGTGCCGAGAGCCGGCTGCTCGGTGGCCGCAACTAGTTCGGCTCAGCTAGTTCCAATGGCAGGG AGGTGCCGAGAGCCGGCTGCTCGGTGGCCGCAGCTAGTTCGGCTCAGCTAGTTCCAATGGCAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:70902357..70902461 26863196 MeRIP-seq:(Medium) rs1428806365 Functional Loss SNV dbSNP153 33..33 33 - - - 102194 RMVar_ID_102194 Human_SNP_ID_188925797 m1A Human chr4 + 70902494 70902494 70902494 TTTCCTCTTCTTTCCTGGCCCACGCCGCTCCGAGGCCTCGCGACCGCCGAGCCTGCAGCCTGCCC TTTCCTCTTCTTTCCTGGCCCACGCCGCTCCGCGGCCTCGCGACCGCCGAGCCTGCAGCCTGCCC A C MOB1B Ensembl:ENSG00000173542 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:70902362..70902527 26863196 MeRIP-seq:(Medium) rs1372487395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9334714 Human_Splice_Rec_567607,Human_Splice_Rec_567617,Human_Splice_Rec_567623,Human_Splice_Rec_567633,Human_Splice_Rec_567645 102195 RMVar_ID_102195 Human_SNP_ID_188949063 m1A Human chr4 + 70993825 70993825 70993825 CCCTCTTTGCCGGACGAGCTCTGGGCCGCCACAAGACTAAGGAATGGCCACCCCGCCCAAGAGAA CCCTCTTTGCCGGACGAGCTCTGGGCCGCCACGAGACTAAGGAATGGCCACCCCGCCCAAGAGAA A G DCK,MOB1B Ensembl:ENSG00000156136,Ensembl:ENSG00000173542 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:70993604..70993860 26863196 MeRIP-seq:(Medium) rs372945476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1640113,Human_RBP_ID_4789543,Human_RBP_ID_8943689,Human_RBP_ID_9304171,Human_RBP_ID_9396366,Human_RBP_ID_22095913,Human_RBP_ID_24062997 Human_Splice_Rec_567656 RMVar_hsa_circ_36034 102196 RMVar_ID_102196 Human_SNP_ID_188949064 m1A Human chr4 + 70993826 70993826 70993826 CCTCTTTGCCGGACGAGCTCTGGGCCGCCACAAGACTAAGGAATGGCCACCCCGCCCAAGAGAAG CCTCTTTGCCGGACGAGCTCTGGGCCGCCACAGGACTAAGGAATGGCCACCCCGCCCAAGAGAAG A G DCK,MOB1B Ensembl:ENSG00000156136,Ensembl:ENSG00000173542 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr4:70993709..70993856;chr4:70993589..70993841 26863196 MeRIP-seq:(Medium) rs1435129843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1640113,Human_RBP_ID_4789543,Human_RBP_ID_8943689,Human_RBP_ID_9304171,Human_RBP_ID_9396366,Human_RBP_ID_22095913,Human_RBP_ID_24062997 Human_Splice_Rec_567656 RMVar_hsa_circ_36034 102197 RMVar_ID_102197 Human_SNP_ID_188949066 m1A Human chr4 + 70993828 70993828 70993828 TCTTTGCCGGACGAGCTCTGGGCCGCCACAAGACTAAGGAATGGCCACCCCGCCCAAGAGAAGCT TCTTTGCCGGACGAGCTCTGGGCCGCCACAAGGCTAAGGAATGGCCACCCCGCCCAAGAGAAGCT A G DCK,MOB1B Ensembl:ENSG00000156136,Ensembl:ENSG00000173542 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:70993638..70993900 26863196 MeRIP-seq:(Medium) rs201444059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1640113,Human_RBP_ID_4789543,Human_RBP_ID_8943689,Human_RBP_ID_9304171,Human_RBP_ID_9396366,Human_RBP_ID_22095913,Human_RBP_ID_24062998 Human_Splice_Rec_567656,Human_Splice_Rec_567669,Human_Splice_Rec_567679,Human_Splice_Rec_567693 RMVar_hsa_circ_36034 102198 RMVar_ID_102198 Human_SNP_ID_189483239 m1A Human chr4 - 73091576 73091576 73091576 ATGCCACCACAACAACAGTCACAACCACGGCAAGCAACAACAACACTGCACCCACAAATGCCACA ATGCCACCACAACAACAGTCACAACCACGGCAGGCAACAACAACACTGCACCCACAAATGCCACA T C ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:73091525..73091626 26863196 MeRIP-seq:(Medium) rs1361208670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17295783,Human_RBP_ID_17409236,Human_RBP_ID_22096272,Human_RBP_ID_22423572 RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_289776,RMVar_hsa_circ_226529,RMVar_hsa_circ_69338,RMVar_hsa_circ_78748,RMVar_hsa_circ_226532,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,RMVar_hsa_circ_272665,RMVar_hsa_circ_309760,RMVar_hsa_circ_365476,RMVar_hsa_circ_375630,RMVar_hsa_circ_297372,RMVar_hsa_circ_53593,RMVar_hsa_circ_226536,RMVar_hsa_circ_226538,RMVar_hsa_circ_226537,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_272131,RMVar_hsa_circ_312455,RMVar_hsa_circ_54454,RMVar_hsa_circ_226540 102199 RMVar_ID_102199 Human_SNP_ID_189524083 m1A Human chr4 - 73258058 73258057 73258059 ACACGTGGGGGTGGGAGGACCACGGAGTTCACAGAGTTGGTGAACAGCCTGTTATCATGGGATGG ACACGTGGGGGTGGGAGGACCACGGAGTTCA__GAGTTGGTGAACAGCCTGTTATCATGGGATGG CTG C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:73258054..73258183 26863196 MeRIP-seq:(Medium) rs1422082485 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_213804,Human_RBP_ID_838163,Human_RBP_ID_1641611,Human_RBP_ID_3747435,Human_RBP_ID_3966827,Human_RBP_ID_5089938,Human_RBP_ID_5210905,Human_RBP_ID_5395315,Human_RBP_ID_8130511,Human_RBP_ID_8211750,Human_RBP_ID_8236510,Human_RBP_ID_9435809,Human_RBP_ID_18955242,Human_RBP_ID_21988663,Human_RBP_ID_24431134,Human_RBP_ID_26349361,Human_RBP_ID_26791614,Human_RBP_ID_27824198 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566 102200 RMVar_ID_102200 Human_SNP_ID_189524084 m1A Human chr4 - 73258058 73258058 73258058 ACACGTGGGGGTGGGAGGACCACGGAGTTCACAGAGTTGGTGAACAGCCTGTTATCATGGGATGG ACACGTGGGGGTGGGAGGACCACGGAGTTCACGGAGTTGGTGAACAGCCTGTTATCATGGGATGG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:73258054..73258183 26863196 MeRIP-seq:(Medium) rs562188943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213804,Human_RBP_ID_838163,Human_RBP_ID_1641611,Human_RBP_ID_3747435,Human_RBP_ID_3966827,Human_RBP_ID_5089938,Human_RBP_ID_5210905,Human_RBP_ID_5395315,Human_RBP_ID_8130511,Human_RBP_ID_8211750,Human_RBP_ID_8236510,Human_RBP_ID_9435809,Human_RBP_ID_18955242,Human_RBP_ID_21988663,Human_RBP_ID_24431134,Human_RBP_ID_26349361,Human_RBP_ID_26791614,Human_RBP_ID_27824198 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566 102201 RMVar_ID_102201 Human_SNP_ID_189524162 m1A Human chr4 - 73258325 73258325 73258325 CGGAGGTGGCGGCGGCGGCACCAGCAGTAACAACAGCGAGGAAGAAGAGGACGACGACGACGAGG CGGAGGTGGCGGCGGCGGCACCAGCAGTAACAGCAGCGAGGAAGAAGAGGACGACGACGACGAGG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:73258205..73258800 26863196 MeRIP-seq:(Medium) rs906955660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71358,Human_RBP_ID_248983,Human_RBP_ID_838045,Human_RBP_ID_2856240,Human_RBP_ID_4789930,Human_RBP_ID_9396394,Human_RBP_ID_23034914,Human_RBP_ID_25835636,Human_RBP_ID_26349363,Human_RBP_ID_27824200 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 102202 RMVar_ID_102202 Human_SNP_ID_189524163 m1A Human chr4 - 73258326 73258326 73258326 GCGGAGGTGGCGGCGGCGGCACCAGCAGTAACAACAGCGAGGAAGAAGAGGACGACGACGACGAG GCGGAGGTGGCGGCGGCGGCACCAGCAGTAACGACAGCGAGGAAGAAGAGGACGACGACGACGAG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:73258224..73258475;chr4:73258167..73258818 26863196 MeRIP-seq:(Medium) rs1202444571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71358,Human_RBP_ID_248983,Human_RBP_ID_838045,Human_RBP_ID_2856240,Human_RBP_ID_4789930,Human_RBP_ID_9396394,Human_RBP_ID_23034914,Human_RBP_ID_26349363,Human_RBP_ID_27824200 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 102203 RMVar_ID_102203 Human_SNP_ID_189524173 m1A Human chr4 - 73258354 73258342 73258354 AGCGGCGGCGGTGGAGGCGGCGGTGGAGGCGGAGGTGGCGGCGGCGGCACCAGCAGTAACAACAG AGCGGCGGCGGTGGAGGCGGCGGTGGAGGCGG____________CGGCACCAGCAGTAACAACAG GCCGCCGCCACCT G ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:73258305..73258669 26863196 MeRIP-seq:(Medium) rs1239060159 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_71358,Human_RBP_ID_838045,Human_RBP_ID_9396394,Human_RBP_ID_23034914 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 102204 RMVar_ID_102204 Human_SNP_ID_189524185 m1A Human chr4 - 73258354 73258354 73258354 AGCGGCGGCGGTGGAGGCGGCGGTGGAGGCGGAGGTGGCGGCGGCGGCACCAGCAGTAACAACAG AGCGGCGGCGGTGGAGGCGGCGGTGGAGGCGGCGGTGGCGGCGGCGGCACCAGCAGTAACAACAG T G ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:73258305..73258669 26863196 MeRIP-seq:(Medium) rs1229181363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71358,Human_RBP_ID_838045,Human_RBP_ID_9396394,Human_RBP_ID_23034914 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 102205 RMVar_ID_102205 Human_SNP_ID_189524344 m1A Human chr4 + 73258630 73258630 73258630 GCCACCGCCGGGGGGCTCCCTTCTCCTTCTGCAGCCGTCGCCGCCGCCACCGGAACCGTCGCCTT GCCACCGCCGGGGGGCTCCCTTCTCCTTCTGCGGCCGTCGCCGCCGCCACCGGAACCGTCGCCTT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:73258583..73258746 26863196 MeRIP-seq:(Medium) rs1446935581 Functional Loss SNV dbSNP153 33..33 33 - - - 102206 RMVar_ID_102206 Human_SNP_ID_189524345 m1A Human chr4 + 73258652 73258631 73258652 CTCCTTCTGCAGCCGTCGCCGCCGCCACCGGAACCGTCGCCTTCTCCATCCCCAGGGAAAGAGGG CTCCTTCTGCAG_____________________CCGTCGCCTTCTCCATCCCCAGGGAAAGAGGG GCCGTCGCCGCCGCCACCGGAA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:73258601..73258754 26863196 MeRIP-seq:(Medium) rs1257476904 Functional Loss DEL dbSNP153 13..33 33 - - - 102207 RMVar_ID_102207 Human_SNP_ID_189524382 m1A Human chr4 - 73258730 73258729 73258730 ACCGATTGCTGTGTCGGCCCCAGTGCGGCCGAAGTCGCGGTAGAGCGTAGCCCCACGCCCCTCCC ACCGATTGCTGTGTCGGCCCCAGTGCGGCCGA_GTCGCGGTAGAGCGTAGCCCCACGCCCCTCCC CT C ANKRD17 Ensembl:ENSG00000132466 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:73258712..73258802 26863410 MeRIP-seq:(Medium) rs1338482659 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_71360,Human_RBP_ID_4794993,Human_RBP_ID_9304177,Human_RBP_ID_9396397,Human_RBP_ID_18424596,Human_RBP_ID_22095564,Human_RBP_ID_26348894,Human_RBP_ID_27824201 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 102208 RMVar_ID_102208 Human_SNP_ID_189524497 m1A Human chr4 + 73258962 73258962 73258962 GAGACCGGGTGTCGGGAGAACCAGAGGAGAGGAGACTGGAAAGAAGCGGGGAAGTGTGCCTGGGG GAGACCGGGTGTCGGGAGAACCAGAGGAGAGGGGACTGGAAAGAAGCGGGGAAGTGTGCCTGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:73258913..73259081 26863196 MeRIP-seq:(Medium) rs1300089092 Functional Loss SNV dbSNP153 33..33 33 - - - 102209 RMVar_ID_102209 Human_SNP_ID_189744355 m1A Human chr4 - 74099120 74099120 74099120 CGCACAGCCGCTCGAACCGCCTGCTGAGCCCCATGGCCCGCGCCACGCTCTCCGCCGCCCCCAGC CGCACAGCCGCTCGAACCGCCTGCTGAGCCCCGTGGCCCGCGCCACGCTCTCCGCCGCCCCCAGC T C CXCL2 Ensembl:ENSG00000081041 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:74099101..74099187 26863410 MeRIP-seq:(Medium) rs1459791750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_569219,Human_Splice_Rec_569229 102210 RMVar_ID_102210 Human_SNP_ID_189758987 m1A Human chr4 + 74158208 74158208 74158208 GCCGCCTTGGCCGAGCGCCGGCGTTGGGCAGAAGCACAGCACCCTCCGTAAGGGCACCGGGAGAG GCCGCCTTGGCCGAGCGCCGGCGTTGGGCAGAGGCACAGCACCCTCCGTAAGGGCACCGGGAGAG A G MTHFD2L Ensembl:ENSG00000163738 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:74158161..74158310 26863196 MeRIP-seq:(Medium) rs1353574820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_837654,Human_RBP_ID_4794994,Human_RBP_ID_19014459,Human_RBP_ID_23034700,Human_RBP_ID_24063768 Human_Splice_Rec_569285,Human_Splice_Rec_569297,Human_Splice_Rec_569311,Human_Splice_Rec_569313,Human_Splice_Rec_569327,Human_Splice_Rec_569341 Human_miRNA_ID_2236340 RMVar_hsa_circ_100789,RMVar_hsa_circ_226587 102211 RMVar_ID_102211 Human_SNP_ID_575625771 m1A Human chr15 + 45040361 45040361 45040361 AATTGTTTTTAATGGAAAATGTTCATAAGGTGAAGTTCTTATGCATGCTAAATGATTTTTTCAAT AATTGTTTTTAATGGAAAATGTTCATAAGGTGGAGTTCTTATGCATGCTAAATGATTTTTTCAAT A G SORD Ensembl:ENSG00000140263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:45040352..45040417 26863196 MeRIP-seq:(Medium) rs1331374478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1596317,Human_Splice_Rec_1596333,Human_Splice_Rec_1596345,Human_Splice_Rec_1596361,Human_Splice_Rec_1596389,Human_Splice_Rec_1596403 102212 RMVar_ID_102212 Human_SNP_ID_575630751 m1A Human chr15 - 45061200 45061200 45061200 ACTAACTTGTAACAAAAGGCTGCATTGTGCTTATAGAACCGGCAGAGGTTCCCGTCATCGGGGGG ACTAACTTGTAACAAAAGGCTGCATTGTGCTTGTAGAACCGGCAGAGGTTCCCGTCATCGGGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:45061176..45061200 26863196 MeRIP-seq:(Medium) rs770320477 Functional Loss SNV dbSNP153 33..33 33 - - - 102213 RMVar_ID_102213 Human_SNP_ID_575634234 m1A Human chr15 - 45073552 45073552 45073552 CCATTGTGCCCTGAGATCCCAAGACTGTGGGGATGAGGGCAGAGCCCATTAACATCAGGGATTCT CCATTGTGCCCTGAGATCCCAAGACTGTGGGGTTGAGGGCAGAGCCCATTAACATCAGGGATTCT T A AC091117.2 Ensembl:ENSG00000259352 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:45073538..45073634 32194978 MeRIP-seq:(Medium) rs767229268 Functional Loss SNV dbSNP153 33..33 33 - - - 102214 RMVar_ID_102214 Human_SNP_ID_575668076 m1A Human chr15 - 45198583 45198583 45198583 AGTCACGGCATTGTGGGAACAATGGCACGGCAAGGGGCTCGGTATTTTTTTCCCCTTTTTTGTAA AGTCACGGCATTGTGGGAACAATGGCACGGCAGGGGGCTCGGTATTTTTTTCCCCTTTTTTGTAA T C SHF,AC051619.6 Ensembl:ENSG00000138606,Ensembl:ENSG00000259932 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:45198505..45198588 26863196 MeRIP-seq:(Medium) rs12324467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814502,Human_RBP_ID_1000788,Human_RBP_ID_1174627,Human_RBP_ID_1278359,Human_RBP_ID_1363265,Human_RBP_ID_1511681,Human_RBP_ID_1829902,Human_RBP_ID_3475184,Human_RBP_ID_5087856,Human_RBP_ID_5464008,Human_RBP_ID_5494395,Human_RBP_ID_5566424,Human_RBP_ID_5646545,Human_RBP_ID_6429735,Human_RBP_ID_8082076,Human_RBP_ID_8183816,Human_RBP_ID_8250986,Human_RBP_ID_8417348,Human_RBP_ID_8800333,Human_RBP_ID_9052724,Human_RBP_ID_12518928,Human_RBP_ID_17250019,Human_RBP_ID_17861003,Human_RBP_ID_18436471,Human_RBP_ID_18512453,Human_RBP_ID_18663331,Human_RBP_ID_20025567,Human_RBP_ID_22496308,Human_RBP_ID_22799785,Human_RBP_ID_23127374,Human_RBP_ID_23653124,Human_RBP_ID_26931796,Human_RBP_ID_27155568,Human_RBP_ID_27232061,Human_RBP_ID_27651142,Human_RBP_ID_27837420 Human_miRNA_ID_3205318 102215 RMVar_ID_102215 Human_SNP_ID_575668088 m1A Human chr15 + 45198593 45198593 45198593 GGGGAAAAAAATACCGAGCCCCTTGCCGTGCCATTGTTCCCACAATGCCGTGACTCGGATTCGAA GGGGAAAAAAATACCGAGCCCCTTGCCGTGCCCTTGTTCCCACAATGCCGTGACTCGGATTCGAA A C AC051619.3 Ensembl:ENSG00000259519 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:45198539..45198650 26863196 MeRIP-seq:(Medium) rs959165836 Functional Loss SNV dbSNP153 33..33 33 - - - 102216 RMVar_ID_102216 Human_SNP_ID_575668089 m1A Human chr15 + 45198593 45198593 45198593 GGGGAAAAAAATACCGAGCCCCTTGCCGTGCCATTGTTCCCACAATGCCGTGACTCGGATTCGAA GGGGAAAAAAATACCGAGCCCCTTGCCGTGCCGTTGTTCCCACAATGCCGTGACTCGGATTCGAA A G AC051619.3 Ensembl:ENSG00000259519 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:45198539..45198650 26863196 MeRIP-seq:(Medium) rs959165836 Functional Loss SNV dbSNP153 33..33 33 - - - 102217 RMVar_ID_102217 Human_SNP_ID_575668093 m1A Human chr15 - 45198598 45198598 45198598 CTCGGTTCGAATCCGAGTCACGGCATTGTGGGAACAATGGCACGGCAAGGGGCTCGGTATTTTTT CTCGGTTCGAATCCGAGTCACGGCATTGTGGGGACAATGGCACGGCAAGGGGCTCGGTATTTTTT T C SHF,AC051619.6 Ensembl:ENSG00000138606,Ensembl:ENSG00000259932 Protein coding,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:45198564..45198812 26863196 MeRIP-seq:(Medium) rs914830901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42940,Human_RBP_ID_458152,Human_RBP_ID_759456,Human_RBP_ID_1000788,Human_RBP_ID_1130310,Human_RBP_ID_1174627,Human_RBP_ID_1363265,Human_RBP_ID_1511681,Human_RBP_ID_1829902,Human_RBP_ID_2441971,Human_RBP_ID_3475184,Human_RBP_ID_5087856,Human_RBP_ID_5258921,Human_RBP_ID_5439656,Human_RBP_ID_5464009,Human_RBP_ID_5566424,Human_RBP_ID_5646545,Human_RBP_ID_6429735,Human_RBP_ID_8082076,Human_RBP_ID_8183816,Human_RBP_ID_8250986,Human_RBP_ID_8417348,Human_RBP_ID_8800333,Human_RBP_ID_9052724,Human_RBP_ID_12518928,Human_RBP_ID_18436471,Human_RBP_ID_18512453,Human_RBP_ID_18663331,Human_RBP_ID_20025567,Human_RBP_ID_22496308,Human_RBP_ID_22799785,Human_RBP_ID_23127374,Human_RBP_ID_23653124,Human_RBP_ID_26931796,Human_RBP_ID_27155568,Human_RBP_ID_27232061,Human_RBP_ID_27651142,Human_RBP_ID_27837420 102218 RMVar_ID_102218 Human_SNP_ID_575668116 m1A Human chr15 - 45198621 45198621 45198621 CTCTGCGTTGTGGCCGCAGCAACCTCGGTTCGAATCCGAGTCACGGCATTGTGGGAACAATGGCA CTCTGCGTTGTGGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCATTGTGGGAACAATGGCA T A SHF,AC051619.6 Ensembl:ENSG00000138606,Ensembl:ENSG00000259932 Protein coding,lincRNA intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs551433634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42940,Human_RBP_ID_1130310,Human_RBP_ID_1174628,Human_RBP_ID_1511681,Human_RBP_ID_1829903,Human_RBP_ID_4343757,Human_RBP_ID_6429735,Human_RBP_ID_8250987,Human_RBP_ID_8417349,Human_RBP_ID_12654782,Human_RBP_ID_17482264,Human_RBP_ID_18663331,Human_RBP_ID_20091784,Human_RBP_ID_22191562,Human_RBP_ID_23113812,Human_RBP_ID_23127374,Human_RBP_ID_23653125,Human_RBP_ID_24412771,Human_RBP_ID_24475169,Human_RBP_ID_26931797,Human_RBP_ID_27232063,Human_RBP_ID_27651143,Human_RBP_ID_27796850,Human_RBP_ID_27837420 102219 RMVar_ID_102219 Human_SNP_ID_575668121 m1A Human chr15 + 45198625 45198625 45198625 ATTGTTCCCACAATGCCGTGACTCGGATTCGAACCGAGGTTGCTGCGGCCACAACGCAGAGTACT ATTGTTCCCACAATGCCGTGACTCGGATTCGAGCCGAGGTTGCTGCGGCCACAACGCAGAGTACT A G AC051619.3 Ensembl:ENSG00000259519 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr15:45198576..45198711;chr15:45198576..45198715 26863196 MeRIP-seq:(Medium) rs535112933 Functional Loss SNV dbSNP153 33..33 33 - - - 102220 RMVar_ID_102220 Human_SNP_ID_575668210 m1A Human chr15 - 45198718 45198718 45198718 GCGCAAACTGGGAAGGCCTATGACTGTTGAAGAGGATAATCAGAAGCCAACCCCTACGGGTCCCC GCGCAAACTGGGAAGGCCTATGACTGTTGAAGGGGATAATCAGAAGCCAACCCCTACGGGTCCCC T C SHF,AC051619.6 Ensembl:ENSG00000138606,Ensembl:ENSG00000259932 Protein coding,lincRNA intron,exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:45198653..45198740 26863410 MeRIP-seq:(Medium) rs764206853 Functional Loss SNV dbSNP153 33..33 33 - - - 102221 RMVar_ID_102221 Human_SNP_ID_575668791 m1A Human chr15 - 45200401 45200401 45200401 GTTCGAATCCGAGTCACGGCATTGTGAGGACAATGGCACGGCAAGGGGAGTTTGTTTTATTGTAC GTTCGAATCCGAGTCACGGCATTGTGAGGACAGTGGCACGGCAAGGGGAGTTTGTTTTATTGTAC T C SHF,AC051619.7 Ensembl:ENSG00000138606,Ensembl:ENSG00000260035 Protein coding,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:45200351..45200456 26863196 MeRIP-seq:(Medium) rs997653288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42941,Human_RBP_ID_1000789,Human_RBP_ID_1130451,Human_RBP_ID_1174631,Human_RBP_ID_1504981,Human_RBP_ID_1829905,Human_RBP_ID_2441973,Human_RBP_ID_3475187,Human_RBP_ID_4343758,Human_RBP_ID_5180535,Human_RBP_ID_5258953,Human_RBP_ID_5418581,Human_RBP_ID_5566425,Human_RBP_ID_6429739,Human_RBP_ID_8250989,Human_RBP_ID_8417354,Human_RBP_ID_8800338,Human_RBP_ID_12518933,Human_RBP_ID_17688526,Human_RBP_ID_18480899,Human_RBP_ID_18512455,Human_RBP_ID_18545367,Human_RBP_ID_18663335,Human_RBP_ID_20025571,Human_RBP_ID_22191563,Human_RBP_ID_22798867,Human_RBP_ID_23113772,Human_RBP_ID_23127380,Human_RBP_ID_23653131,Human_RBP_ID_26931798,Human_RBP_ID_27155570,Human_RBP_ID_27435414,Human_RBP_ID_27651144 Human_miRNA_ID_3164675 102222 RMVar_ID_102222 Human_SNP_ID_575668792 m1A Human chr15 - 45200402 45200402 45200402 GGTTCGAATCCGAGTCACGGCATTGTGAGGACAATGGCACGGCAAGGGGAGTTTGTTTTATTGTA GGTTCGAATCCGAGTCACGGCATTGTGAGGACGATGGCACGGCAAGGGGAGTTTGTTTTATTGTA T C SHF,AC051619.7 Ensembl:ENSG00000138606,Ensembl:ENSG00000260035 Protein coding,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:45200305..45200479 26863196 MeRIP-seq:(Medium) rs1023460347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42941,Human_RBP_ID_1000789,Human_RBP_ID_1130451,Human_RBP_ID_1174631,Human_RBP_ID_1504981,Human_RBP_ID_1829905,Human_RBP_ID_2441973,Human_RBP_ID_3475187,Human_RBP_ID_4343758,Human_RBP_ID_5087817,Human_RBP_ID_5180535,Human_RBP_ID_5258953,Human_RBP_ID_5418581,Human_RBP_ID_5566425,Human_RBP_ID_6429739,Human_RBP_ID_8250989,Human_RBP_ID_8417354,Human_RBP_ID_8800338,Human_RBP_ID_12518933,Human_RBP_ID_17119149,Human_RBP_ID_17688526,Human_RBP_ID_18480899,Human_RBP_ID_18512455,Human_RBP_ID_18545367,Human_RBP_ID_18663335,Human_RBP_ID_20025571,Human_RBP_ID_22191563,Human_RBP_ID_22798867,Human_RBP_ID_23113772,Human_RBP_ID_23127380,Human_RBP_ID_23653131,Human_RBP_ID_26931798,Human_RBP_ID_27155570,Human_RBP_ID_27435414,Human_RBP_ID_27651144 Human_miRNA_ID_3164675 102223 RMVar_ID_102223 Human_SNP_ID_575668812 m1A Human chr15 - 45200418 45200418 45200418 TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCACGGCATTGTGAGGACAATGGCACGGCAAGGGG TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCGCGGCATTGTGAGGACAATGGCACGGCAAGGGG T C SHF,AC051619.7 Ensembl:ENSG00000138606,Ensembl:ENSG00000260035 Protein coding,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:45200376..45200514 26863196 MeRIP-seq:(Medium) rs917822614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42941,Human_RBP_ID_232454,Human_RBP_ID_759457,Human_RBP_ID_814632,Human_RBP_ID_1504982,Human_RBP_ID_1829906,Human_RBP_ID_3475187,Human_RBP_ID_4343758,Human_RBP_ID_5087817,Human_RBP_ID_5180441,Human_RBP_ID_5258953,Human_RBP_ID_5646558,Human_RBP_ID_6429741,Human_RBP_ID_8183641,Human_RBP_ID_8250989,Human_RBP_ID_8417355,Human_RBP_ID_8800338,Human_RBP_ID_12518933,Human_RBP_ID_17077271,Human_RBP_ID_18480899,Human_RBP_ID_18545367,Human_RBP_ID_18663335,Human_RBP_ID_20025571,Human_RBP_ID_22531515,Human_RBP_ID_22798868,Human_RBP_ID_23113772,Human_RBP_ID_23127380,Human_RBP_ID_23653131,Human_RBP_ID_24473636,Human_RBP_ID_24531025,Human_RBP_ID_25184368,Human_RBP_ID_27651144 Human_miRNA_ID_3164675 102224 RMVar_ID_102224 Human_SNP_ID_575668851 m1A Human chr15 + 45200474 45200474 45200474 CTGCGGCCACAACGCAGAGTACTAACCACTATACGATCACGGCGAGCTACTAGGGACACAGGACC CTGCGGCCACAACGCAGAGTACTAACCACTATGCGATCACGGCGAGCTACTAGGGACACAGGACC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:45200318..45200500 26863410 MeRIP-seq:(Medium) rs1172988319 Functional Loss SNV dbSNP153 33..33 33 - - - 102225 RMVar_ID_102225 Human_SNP_ID_575668852 m1A Human chr15 + 45200474 45200474 45200474 CTGCGGCCACAACGCAGAGTACTAACCACTATACGATCACGGCGAGCTACTAGGGACACAGGACC CTGCGGCCACAACGCAGAGTACTAACCACTATTCGATCACGGCGAGCTACTAGGGACACAGGACC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:45200318..45200500 26863410 MeRIP-seq:(Medium) rs1172988319 Functional Loss SNV dbSNP153 33..33 33 - - - 102226 RMVar_ID_102226 Human_SNP_ID_575716636 m1A Human chr15 - 45402456 45402456 45402456 TCTAAGGGTAGCAGCTTTAAGAGCGGCCCTTCAGGGAAGGGATCCGAGTCCGGAGCCATCGCACA TCTAAGGGTAGCAGCTTTAAGAGCGGCCCTTCGGGGAAGGGATCCGAGTCCGGAGCCATCGCACA T C lnc-GATM-1 RNACentral:URS00008B8A90 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:45402409..45402509 26863196 MeRIP-seq:(Medium) rs1484754417 Functional Loss SNV dbSNP153 33..33 33 - - - 102227 RMVar_ID_102227 Human_SNP_ID_576445952 m1A Human chr15 + 48331270 48331270 48331270 AAAAATGGGGGCCAGAGCAAACAAGAAGAGCGAAAGCAAGAGGGCTAGGCAGCCAGAGGCGGCAG AAAAATGGGGGCCAGAGCAAACAAGAAGAGCGTAAGCAAGAGGGCTAGGCAGCCAGAGGCGGCAG A T DUT Ensembl:ENSG00000128951 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:48331211..48331311 26863196 MeRIP-seq:(Medium) rs933956049 Functional Loss SNV dbSNP153 33..33 33 - - - 102228 RMVar_ID_102228 Human_SNP_ID_576446113 m1A Human chr15 + 48331586 48331586 48331586 TTTCCTTACGTCTCTGCTTCGCTCAGCGATGCAAAACGCGCGAGGCGCACGGCAGAGGGCCGAAG TTTCCTTACGTCTCTGCTTCGCTCAGCGATGCCAAACGCGCGAGGCGCACGGCAGAGGGCCGAAG A C DUT Ensembl:ENSG00000128951 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:48331540..48331644 32194978 MeRIP-seq:(Medium) rs1279609706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1174677,Human_RBP_ID_4342657,Human_RBP_ID_9324264,Human_RBP_ID_19069169,Human_RBP_ID_24551718 RMVar_hsa_circ_266677 102229 RMVar_ID_102229 Human_SNP_ID_576446466 m1A Human chr15 - 48332290 48332290 48332290 ATGCCGCCCACCTCCGCAGGCCGGGCCCGCTTACTGGGTGAAATGGCGGGTGTCTCTTCAGAGCA ATGCCGCCCACCTCCGCAGGCCGGGCCCGCTTGCTGGGTGAAATGGCGGGTGTCTCTTCAGAGCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:48332208..48332340 26863196 MeRIP-seq:(Medium) rs1289579744 Functional Loss SNV dbSNP153 33..33 33 - - - 102230 RMVar_ID_102230 Human_SNP_ID_576446476 m1A Human chr15 - 48332305 48332305 48332305 GCAAAGCGGAGCTGCATGCCGCCCACCTCCGCAGGCCGGGCCCGCTTACTGGGTGAAATGGCGGG GCAAAGCGGAGCTGCATGCCGCCCACCTCCGCTGGCCGGGCCCGCTTACTGGGTGAAATGGCGGG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:48332176..48332474 26863196 MeRIP-seq:(Medium) rs374290406 Functional Loss SNV dbSNP153 33..33 33 - - - 102231 RMVar_ID_102231 Human_SNP_ID_576446477 m1A Human chr15 - 48332305 48332305 48332305 GCAAAGCGGAGCTGCATGCCGCCCACCTCCGCAGGCCGGGCCCGCTTACTGGGTGAAATGGCGGG GCAAAGCGGAGCTGCATGCCGCCCACCTCCGCGGGCCGGGCCCGCTTACTGGGTGAAATGGCGGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:48332176..48332474 26863196 MeRIP-seq:(Medium) rs374290406 Functional Loss SNV dbSNP153 33..33 33 - - - 102232 RMVar_ID_102232 Human_SNP_ID_576447004 m1A Human chr15 + 48334404 48334404 48334404 TTTTATAAATAGATTTGCAGTTATTTTCTTTCAATATTTTCTTAGTGCCTATGATTACACAATAC TTTTATAAATAGATTTGCAGTTATTTTCTTTCGATATTTTCTTAGTGCCTATGATTACACAATAC A G DUT Ensembl:ENSG00000128951 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:48334401..48334525 32194978 MeRIP-seq:(Medium) rs1047322990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6430997,Human_RBP_ID_17861252,Human_RBP_ID_26631788 RMVar_hsa_circ_266677 102233 RMVar_ID_102233 Human_SNP_ID_576448655 m1A Human chr15 + 48341575 48341572 48341575 CATTTGCGAACGGATTTTTTATCCAGAAATAGAAGAAGTTCAAGTAAGTATTACAAAGGAAGATA CATTTGCGAACGGATTTTTTATCCAGAAAT___AGAAGTTCAAGTAAGTATTACAAAGGAAGATA TAGA T DUT Ensembl:ENSG00000128951 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs774179371 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17870371,Human_RBP_ID_19068132 Human_Splice_Rec_1599032,Human_Splice_Rec_1599033,Human_Splice_Rec_1599044,Human_Splice_Rec_1599045,Human_Splice_Rec_1599056,Human_Splice_Rec_1599057,Human_Splice_Rec_1599068,Human_Splice_Rec_1599069,Human_Splice_Rec_1599081,Human_Splice_Rec_1599090,Human_Splice_Rec_1599091,Human_Splice_Rec_1599106,Human_Splice_Rec_1599107,Human_Splice_Rec_1599114,Human_Splice_Rec_1599115 RMVar_hsa_circ_111435,RMVar_hsa_circ_18139,RMVar_hsa_circ_171760 102234 RMVar_ID_102234 Human_SNP_ID_576522489 m1A Human chr15 + 48646149 48646149 48646149 TGTTCCACCTGCACCAAGAATGCGCGCTGGAGACGGTTGCCCCGGAGGCCCTGGCCCGAGAGAAA TGTTCCACCTGCACCAAGAATGCGCGCTGGAGGCGGTTGCCCCGGAGGCCCTGGCCCGAGAGAAA A G AC084757.3 Ensembl:ENSG00000259705 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:48646124..48646209 26863410 MeRIP-seq:(Medium) rs537241615 Functional Loss SNV dbSNP153 33..33 33 - - - 102235 RMVar_ID_102235 Human_SNP_ID_576561198 m1A Human chr15 + 48811014 48811014 48811014 CCGCGAGGAAACTCTAGTCCTGGCGGAAGACCAACTTCTAGCAGATCCCCTTACCCTGGCTCTAG CCGCGAGGAAACTCTAGTCCTGGCGGAAGACCTACTTCTAGCAGATCCCCTTACCCTGGCTCTAG A T AC012379.2 Ensembl:ENSG00000259700 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:48810914..48811020 26863196 MeRIP-seq:(Medium) rs1000613525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1599642 102236 RMVar_ID_102236 Human_SNP_ID_576576920 m1A Human chr15 - 48878297 48878297 48878297 CTGTTGGGCCCCGCTGCGGGAGGGACGCAGGGATAGCTCCCGGCTCCCGCTGCCTACCTCCATCT CTGTTGGGCCCCGCTGCGGGAGGGACGCAGGGGTAGCTCCCGGCTCCCGCTGCCTACCTCCATCT T C SHC4 Ensembl:ENSG00000185634 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:48878250..48878425 26863196 MeRIP-seq:(Medium) rs1306756618 Functional Loss SNV dbSNP153 33..33 33 - - - 102237 RMVar_ID_102237 Human_SNP_ID_576576935 m1A Human chr15 + 48878325 48878325 48878325 GCTATCCCTGCGTCCCTCCCGCAGCGGGGCCCAACAGCTCGAGGAGGAAGGCCCAATGGAGGAGG GCTATCCCTGCGTCCCTCCCGCAGCGGGGCCCCACAGCTCGAGGAGGAAGGCCCAATGGAGGAGG A C EID1 Ensembl:ENSG00000255302 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:48878151..48878550 32194978 MeRIP-seq:(Medium) rs1225860363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343526,Human_RBP_ID_5646489,Human_RBP_ID_8183659,Human_RBP_ID_8804298,Human_RBP_ID_9284201,Human_RBP_ID_10483000,Human_RBP_ID_17669480,Human_RBP_ID_17861378,Human_RBP_ID_18409344,Human_RBP_ID_18926481,Human_RBP_ID_22355820,Human_RBP_ID_22439788,Human_RBP_ID_22497100,Human_RBP_ID_26326692 Human_miRNA_ID_1848595 102238 RMVar_ID_102238 Human_SNP_ID_576576953 m1A Human chr15 + 48878361 48878361 48878361 GCTCGAGGAGGAAGGCCCAATGGAGGAGGAGGAGGCCCAGCCAATGGCGGCGCCAGAGGGGAAAC GCTCGAGGAGGAAGGCCCAATGGAGGAGGAGGCGGCCCAGCCAATGGCGGCGCCAGAGGGGAAAC A C EID1 Ensembl:ENSG00000255302 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:48878314..48878475 26863196 MeRIP-seq:(Medium) rs752702144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5646489,Human_RBP_ID_6484322,Human_RBP_ID_8251565,Human_RBP_ID_8804299,Human_RBP_ID_9284201,Human_RBP_ID_10483000,Human_RBP_ID_18409344,Human_RBP_ID_19070135,Human_RBP_ID_21959739,Human_RBP_ID_26326693 Human_Splice_Rec_1599722 102239 RMVar_ID_102239 Human_SNP_ID_576576971 m1A Human chr15 - 48878404 48878404 48878404 TGGCCTGGCTGCTCCCCAGCGTTGGGCCCGTTAGCAAGGCTCCGTTTCCCCTCTGGCGCCGCCAT TGGCCTGGCTGCTCCCCAGCGTTGGGCCCGTTGGCAAGGCTCCGTTTCCCCTCTGGCGCCGCCAT T C SHC4 Ensembl:ENSG00000185634 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:48878311..48878493 26863196 MeRIP-seq:(Medium) rs768172432 Functional Loss SNV dbSNP153 33..33 33 - - - 102240 RMVar_ID_102240 Human_SNP_ID_576577016 m1A Human chr15 + 48878475 48878475 48878475 GGGCGCAGACTTCGAGAGCGAGGACGAGGGCGAGGAATTTGATGACTGGGAGGACGACTACGACT GGGCGCAGACTTCGAGAGCGAGGACGAGGGCGGGGAATTTGATGACTGGGAGGACGACTACGACT A G EID1 Ensembl:ENSG00000255302 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:48878451..48878475 26863196 MeRIP-seq:(Medium) rs1453297247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232468,Human_RBP_ID_1130468,Human_RBP_ID_1505156,Human_RBP_ID_3490182,Human_RBP_ID_4323922,Human_RBP_ID_5096302,Human_RBP_ID_6431771,Human_RBP_ID_8251566,Human_RBP_ID_8417768,Human_RBP_ID_12521247,Human_RBP_ID_17586789,Human_RBP_ID_17669481,Human_RBP_ID_17673208,Human_RBP_ID_18529418,Human_RBP_ID_22388440,Human_RBP_ID_23654046,Human_RBP_ID_26326694,Human_RBP_ID_27435458 102241 RMVar_ID_102241 Human_SNP_ID_576577023 m1A Human chr15 + 48878499 48878499 48878499 CGAGGGCGAGGAATTTGATGACTGGGAGGACGACTACGACTATCCCGAAGAGGAGCAGCTCAGTG CGAGGGCGAGGAATTTGATGACTGGGAGGACGTCTACGACTATCCCGAAGAGGAGCAGCTCAGTG A T EID1 Ensembl:ENSG00000255302 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:48878476..48878500 26863196 MeRIP-seq:(Medium) rs1287590414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232468,Human_RBP_ID_1505156,Human_RBP_ID_1830093,Human_RBP_ID_3490182,Human_RBP_ID_4323922,Human_RBP_ID_5087749,Human_RBP_ID_5096302,Human_RBP_ID_6431771,Human_RBP_ID_8251566,Human_RBP_ID_9256611,Human_RBP_ID_9284202,Human_RBP_ID_9340908,Human_RBP_ID_9418985,Human_RBP_ID_9816067,Human_RBP_ID_10483001,Human_RBP_ID_12521247,Human_RBP_ID_17188381,Human_RBP_ID_17368028,Human_RBP_ID_17669481,Human_RBP_ID_17673208,Human_RBP_ID_17870947,Human_RBP_ID_18161817,Human_RBP_ID_18481473,Human_RBP_ID_18529418,Human_RBP_ID_18544324,Human_RBP_ID_20091112,Human_RBP_ID_21970728,Human_RBP_ID_22047463,Human_RBP_ID_22388440,Human_RBP_ID_26326694 102242 RMVar_ID_102242 Human_SNP_ID_576577207 m1A Human chr15 - 48879084 48879084 48879084 GGCTTTTGTATTGGCAGTTTGTCTTGGTCATGACTTATTCTTGCAAAACCATCTTTACAGCAAAC GGCTTTTGTATTGGCAGTTTGTCTTGGTCATGGCTTATTCTTGCAAAACCATCTTTACAGCAAAC T C SHC4 Ensembl:ENSG00000185634 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:48879034..48879234 32194978 MeRIP-seq:(Medium) rs1242662159 Functional Loss SNV dbSNP153 33..33 33 - - - 102243 RMVar_ID_102243 Human_SNP_ID_576617675 m1A Human chr15 - 49046376 49046376 49046376 GGGGCGGAGGTCCGGAACCCAGTCTGGACCCGAGCGGGGGGCCATGGAGAAAGCGGCCCGAGGCG GGGGCGGAGGTCCGGAACCCAGTCTGGACCCGGGCGGGGGGCCATGGAGAAAGCGGCCCGAGGCG T C SECISBP2L Ensembl:ENSG00000138593 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:49046328..49046402 26863196 MeRIP-seq:(Medium) rs1227620175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_124635,Human_RBP_ID_4343091 102244 RMVar_ID_102244 Human_SNP_ID_576636083 m1A Human chr15 - 49120758 49120758 49120758 CTAGGACAGGAGAAGTGGGTAAGATCAGGATAAGGCTGACAAGGATTTGCTTATGAGTTGAAATT CTAGGACAGGAGAAGTGGGTAAGATCAGGATATGGCTGACAAGGATTTGCTTATGAGTTGAAATT T A COPS2 Ensembl:ENSG00000166200 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:49120709..49121048 26863196 MeRIP-seq:(Medium) rs1053315012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1278445,Human_RBP_ID_12521734 102245 RMVar_ID_102245 Human_SNP_ID_576636093 m1A Human chr15 + 49120804 49120800 49120804 CCCACTTCTCCTGTCCTAGTCCAAAAATCTCCATCATTTCACCCAGACTTCTGCAATGGACTCCT CCCACTTCTCCTGTCCTAGTCCAAAAATC____TCATTTCACCCAGACTTCTGCAATGGACTCCT CTCCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:49120755..49120944 26863196 MeRIP-seq:(Medium) rs1196519982 Functional Loss DEL dbSNP153 30..33 33 - - - 102246 RMVar_ID_102246 Human_SNP_ID_576644800 m1A Human chr15 + 49155881 49155881 49155881 GTCGGAAACTGCGCTCGCATCGAGCAGTTTCCAGCCTCCTGGGTAAAGGAGCAGTCTCCTCCCTT GTCGGAAACTGCGCTCGCATCGAGCAGTTTCCGGCCTCCTGGGTAAAGGAGCAGTCTCCTCCCTT A G GALK2 Ensembl:ENSG00000156958 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:49155833..49155910 26863196 MeRIP-seq:(Medium) rs1246715127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27810275 102247 RMVar_ID_102247 Human_SNP_ID_576683304 m1A Human chr15 + 49321096 49321096 49321096 AATGACAATTAAAAATAATTTGAATGGTAGTGATAAGTGCTATGGAAAAAAATGAGAAGGAATAG AATGACAATTAAAAATAATTTGAATGGTAGTGGTAAGTGCTATGGAAAAAAATGAGAAGGAATAG A G GALK2 Ensembl:ENSG00000156958 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:49321093..49321317 26863196 MeRIP-seq:(Medium) rs1312659429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1278461 RMVar_hsa_circ_34318,RMVar_hsa_circ_73701,RMVar_hsa_circ_290466,RMVar_hsa_circ_171843,RMVar_hsa_circ_272074,RMVar_hsa_circ_21465,RMVar_hsa_circ_318610 102248 RMVar_ID_102248 Human_SNP_ID_576755474 m1A Human chr15 + 49621121 49621121 49621121 GTGTGGAGCTGTTCGAGGACTCGCGGGTGTGCAGGTCTGAGTACCACTCCGATCCCTGGTGGAGG GTGTGGAGCTGTTCGAGGACTCGCGGGTGTGCGGGTCTGAGTACCACTCCGATCCCTGGTGGAGG A G DTWD1 Ensembl:ENSG00000104047 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:49621081..49621161 26863196 MeRIP-seq:(Medium) rs1312393032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342666,Human_RBP_ID_5354454,Human_RBP_ID_19067220,Human_RBP_ID_22934565 Human_Splice_Rec_1600397,Human_Splice_Rec_1600403,Human_Splice_Rec_1600411,Human_Splice_Rec_1600419,Human_Splice_Rec_1600427,Human_Splice_Rec_1600431,Human_Splice_Rec_1600441,Human_Splice_Rec_1600445,Human_Splice_Rec_1600453,Human_Splice_Rec_1600463 RMVar_hsa_circ_102418,RMVar_hsa_circ_171855 102249 RMVar_ID_102249 Human_SNP_ID_576890081 m1A Human chr15 + 50182341 50182341 50182341 GTCCCGCCGCGTGCGCCCCGGCGCAGCCCGCCAGTCCGCCCGGAGCCCGCCCAGTCGCCGCGCTG GTCCCGCCGCGTGCGCCCCGGCGCAGCCCGCCGGTCCGCCCGGAGCCCGCCCAGTCGCCGCGCTG A G SLC27A2 Ensembl:ENSG00000140284 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:50182244..50182468 26863410 MeRIP-seq:(Medium) rs540808334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342275,Human_RBP_ID_5523701,Human_RBP_ID_22440003 102250 RMVar_ID_102250 Human_SNP_ID_576897171 m1A Human chr15 + 50209419 50209419 50209419 CAGGAAGGTTCGCCAGGGAAGGTGGGCTTTGAAGAGTACGGAGAAGTTCTGCAGCCAGGCAAGAA CAGGAAGGTTCGCCAGGGAAGGTGGGCTTTGAGGAGTACGGAGAAGTTCTGCAGCCAGGCAAGAA A G SLC27A2 Ensembl:ENSG00000140284 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50209406..50209491 26863196 MeRIP-seq:(Medium) rs1447361807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22522945 102251 RMVar_ID_102251 Human_SNP_ID_576926344 m1A Human chr15 - 50330441 50330441 50330441 TGGATGAAGTAAATGTGTGAGGCAGTTGATAGAGGGACTCAAATTGCAAGGTGAGATCTTGTGAT TGGATGAAGTAAATGTGTGAGGCAGTTGATAGTGGGACTCAAATTGCAAGGTGAGATCTTGTGAT T A GABPB1 Ensembl:ENSG00000104064 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50330436..50330600 26863196 MeRIP-seq:(Medium) rs1308733692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12523197,Human_RBP_ID_23654526 RMVar_hsa_circ_29802,RMVar_hsa_circ_81405,RMVar_hsa_circ_171877,RMVar_hsa_circ_122669,RMVar_hsa_circ_171892 102252 RMVar_ID_102252 Human_SNP_ID_576932659 m1A Human chr15 - 50354261 50354261 50354261 CGTTCTGAAGGCTCGGGACTTCTGCCCCAAAGACTTCGCCGCCGAGAACTGCGGGTGCACTGCCT CGTTCTGAAGGCTCGGGACTTCTGCCCCAAAGCCTTCGCCGCCGAGAACTGCGGGTGCACTGCCT T G GABPB1-IT1,GABPB1 Ensembl:ENSG00000285410,Ensembl:ENSG00000104064 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:50354259..50354588 26863196 MeRIP-seq:(Medium) rs1251909660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5096298,Human_RBP_ID_22047468,Human_RBP_ID_27435527 RMVar_hsa_circ_81405,RMVar_hsa_circ_171877 102253 RMVar_ID_102253 Human_SNP_ID_576933060 m1A Human chr15 + 50355037 50355037 50355037 GCGACGGGAAGGCAGCAGGAGGTGGTGCGGGGACCCGAGGCGCCTCGTACCCGGCCGGGCTGACG GCGACGGGAAGGCAGCAGGAGGTGGTGCGGGGTCCCGAGGCGCCTCGTACCCGGCCGGGCTGACG A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50354986..50355181 26863196 MeRIP-seq:(Medium) rs1256010299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095877,Human_RBP_ID_5570103,Human_RBP_ID_9371542,Human_RBP_ID_18418358,Human_RBP_ID_22048211,Human_RBP_ID_27232203 102254 RMVar_ID_102254 Human_SNP_ID_576933068 m1A Human chr15 + 50355053 50355053 50355053 AGGAGGTGGTGCGGGGACCCGAGGCGCCTCGTACCCGGCCGGGCTGACGCGGCCCCGCTACACAC AGGAGGTGGTGCGGGGACCCGAGGCGCCTCGTCCCCGGCCGGGCTGACGCGGCCCCGCTACACAC A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:50355003..50355121 26863196 MeRIP-seq:(Medium) rs776189026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4324272,Human_RBP_ID_18418358 102255 RMVar_ID_102255 Human_SNP_ID_576933069 m1A Human chr15 + 50355053 50355053 50355053 AGGAGGTGGTGCGGGGACCCGAGGCGCCTCGTACCCGGCCGGGCTGACGCGGCCCCGCTACACAC AGGAGGTGGTGCGGGGACCCGAGGCGCCTCGTTCCCGGCCGGGCTGACGCGGCCCCGCTACACAC A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:50355003..50355121 26863196 MeRIP-seq:(Medium) rs776189026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4324272,Human_RBP_ID_18418358 102256 RMVar_ID_102256 Human_SNP_ID_576933351 m1A Human chr15 - 50355530 50355530 50355530 TCCAAACTCCTACCCACCGCAGAACAGGCGGGAAGGTTCGGTGGCCACCCGGCCTCTCCGCCGCG TCCAAACTCCTACCCACCGCAGAACAGGCGGGCAGGTTCGGTGGCCACCCGGCCTCTCCGCCGCG T G lnc-TRPM7-1 RNACentral:URS00008B55F7 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:50355483..50355574 26863196 MeRIP-seq:(Medium) rs1232058293 Functional Loss SNV dbSNP153 33..33 33 - - - 102257 RMVar_ID_102257 Human_SNP_ID_576935667 m1A Human chr15 + 50363599 50363599 50363599 TAGAGATGGGGTTTTGCCATGTTGCCCAGGCTAGTCTTGAACTCCTGAGCTCAAGCGAGACACCC TAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGCGAGACACCC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1313821614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247046,Human_RBP_ID_25143603 102258 RMVar_ID_102258 Human_SNP_ID_577032154 m1A Human chr15 + 50717013 50717013 50717013 CCCTGTTGCCTTTCCTTCATCACCATCCCCCCACTCAGTTTCCCAATCCAGAAGCCCTGAACTCT CCCTGTTGCCTTTCCTTCATCACCATCCCCCCGCTCAGTTTCCCAATCCAGAAGCCCTGAACTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:50716963..50717147 26863196 MeRIP-seq:(Medium) rs981325812 Functional Loss SNV dbSNP153 33..33 33 - - - 102259 RMVar_ID_102259 Human_SNP_ID_577044546 m1A Human chr15 - 50765623 50765623 50765623 GGCCGCCCGCGCCTGTCCGGTCCGGTCCGGCCACGGAGGCAGCGCAGCGGCGGGACTCCGAGCCT GGCCGCCCGCGCCTGTCCGGTCCGGTCCGGCCGCGGAGGCAGCGCAGCGGCGGGACTCCGAGCCT T C SPPL2A Ensembl:ENSG00000138600 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50765577..50765646 26863196 MeRIP-seq:(Medium) rs1163173655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232132,Human_RBP_ID_814924,Human_RBP_ID_4342282,Human_RBP_ID_22440006 Human_miRNA_ID_2027424,Human_miRNA_ID_2465023 RMVar_hsa_circ_171987,RMVar_hsa_circ_116964,RMVar_hsa_circ_172005 102260 RMVar_ID_102260 Human_SNP_ID_577080045 m1A Human chr15 - 50908021 50908021 50908021 TCAGCAGGTCGCAGTTGAAAGGTCATCCTTCTAGAGCCCACTCCCCTGGCCCGGCGGGCAAGGAT TCAGCAGGTCGCAGTTGAAAGGTCATCCTTCTGGAGCCCACTCCCCTGGCCCGGCGGGCAAGGAT T C AC021752.1 Ensembl:ENSG00000273674 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50908003..50908101 26863196 MeRIP-seq:(Medium) rs2614787 Functional Loss SNV dbSNP153 33..33 33 - - - 102261 RMVar_ID_102261 Human_SNP_ID_577080310 m1A Human chr15 + 50908707 50908707 50908707 AAACAGGAAGTGCCTACGGAGGCCGGGCCGGCAGCGGCGGCCGGGCATGAAGCCGGGCGGCTACG AAACAGGAAGTGCCTACGGAGGCCGGGCCGGCTGCGGCGGCCGGGCATGAAGCCGGGCGGCTACG A T AP4E1 Ensembl:ENSG00000081014 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:50908702..50908834 26863196 MeRIP-seq:(Medium) rs995543214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4324588,Human_RBP_ID_18418460 102262 RMVar_ID_102262 Human_SNP_ID_577080362 m1A Human chr15 - 50908761 50908757 50908761 CACTATGTCGCTCATCGCCGCCGCCGCCCGCGATGCCGCCGCCGCCCGCGATCCCGTAGCCGCCC CACTATGTCGCTCATCGCCGCCGCCGCCCGCG____CGCCGCCGCCCGCGATCCCGTAGCCGCCC GGCAT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:50908713..50908859 26863196 MeRIP-seq:(Medium) rs747259387 Functional Loss DEL dbSNP153 33..36 33 - - - 102263 RMVar_ID_102263 Human_SNP_ID_577087828 m1A Human chr15 + 50937692 50937692 50937692 ATTTACTGATGTGATAGGACCCTGAAAGGTAGATAAGATTTAGATAGGCAGAAGGGAGATTGAAG ATTTACTGATGTGATAGGACCCTGAAAGGTAGGTAAGATTTAGATAGGCAGAAGGGAGATTGAAG A G AP4E1 Ensembl:ENSG00000081014 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:50937690..50937755 26863196 MeRIP-seq:(Medium) rs1567222307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340872,RMVar_hsa_circ_356982,RMVar_hsa_circ_285853,RMVar_hsa_circ_172010,RMVar_hsa_circ_26905,RMVar_hsa_circ_172011,RMVar_hsa_circ_64629,RMVar_hsa_circ_33308,RMVar_hsa_circ_43699,RMVar_hsa_circ_48840,RMVar_hsa_circ_85453,RMVar_hsa_circ_360028,RMVar_hsa_circ_172016,RMVar_hsa_circ_35121,RMVar_hsa_circ_16526,RMVar_hsa_circ_335899 102264 RMVar_ID_102264 Human_SNP_ID_577254424 m1A Human chr15 - 51622729 51622729 51622729 CTGAGCGGCGACCCGGGCGGCGGCGGCGGTCGAGGAGCTCCCATGGCAGGGACGAGGCGGAGGGA CTGAGCGGCGACCCGGGCGGCGGCGGCGGTCGGGGAGCTCCCATGGCAGGGACGAGGCGGAGGGA T C DMXL2 Ensembl:ENSG00000104093 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:51622578..51622931 26863196 MeRIP-seq:(Medium) rs911537656 Functional Loss SNV dbSNP153 33..33 33 - - - 102265 RMVar_ID_102265 Human_SNP_ID_577254425 m1A Human chr15 - 51622729 51622729 51622729 CTGAGCGGCGACCCGGGCGGCGGCGGCGGTCGAGGAGCTCCCATGGCAGGGACGAGGCGGAGGGA CTGAGCGGCGACCCGGGCGGCGGCGGCGGTCGCGGAGCTCCCATGGCAGGGACGAGGCGGAGGGA T G DMXL2 Ensembl:ENSG00000104093 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:51622578..51622931 26863196 MeRIP-seq:(Medium) rs911537656 Functional Loss SNV dbSNP153 33..33 33 - - - 102266 RMVar_ID_102266 Human_SNP_ID_577282595 m1A Human chr15 - 51737602 51737602 51737602 TCGGCAGGACCCATGGCGGATTCCTCGCCCGCACTGTCCCTGCGGGAAGGCGGCCCCCGCGCGCC TCGGCAGGACCCATGGCGGATTCCTCGCCCGCCCTGTCCCTGCGGGAAGGCGGCCCCCGCGCGCC T G LYSMD2 Ensembl:ENSG00000140280 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:51737527..51737617 26863196 MeRIP-seq:(Medium) rs1303289213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342686 102267 RMVar_ID_102267 Human_SNP_ID_577304834 m1A Human chr15 + 51829719 51829719 51829719 AGTGAGGGAGCTGCTGGCGGGTGGGTCTGGCAACTCTTTGGGAGGCCGACGCGGGCGGACCGGCG AGTGAGGGAGCTGCTGGCGGGTGGGTCTGGCACCTCTTTGGGAGGCCGACGCGGGCGGACCGGCG A C TMOD3 Ensembl:ENSG00000138594 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:51829651..51829870;chr15:51829651..51829962 26863196 MeRIP-seq:(Medium) rs1567256827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759489,Human_RBP_ID_4342687,Human_RBP_ID_5316075,Human_RBP_ID_18418588,Human_RBP_ID_22440313,Human_RBP_ID_26327543,Human_RBP_ID_26768776 102268 RMVar_ID_102268 Human_SNP_ID_577309821 m1A Human chr15 + 51851081 51851081 51851081 GTGGGGTTTTGCCAGAGGAGTTCCAGAGAGACACAGTCAAAGATGTTGAGAGTTATGGAGGGGCA GTGGGGTTTTGCCAGAGGAGTTCCAGAGAGACGCAGTCAAAGATGTTGAGAGTTATGGAGGGGCA A G TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:51851076..51851201 26863196 MeRIP-seq:(Medium) rs568202770 Functional Loss SNV dbSNP153 33..33 33 - - - 102269 RMVar_ID_102269 Human_SNP_ID_577338701 m1A Human chr15 + 51966009 51966009 51966009 GCTGAGGCCTCTCCTCATCATCTGTGTTCTGCATTTTCTCATCATCGTCAGAATTCTGCAGCTTA GCTGAGGCCTCTCCTCATCATCTGTGTTCTGCGTTTTCTCATCATCGTCAGAATTCTGCAGCTTA A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:51965969..51966101 26863196 MeRIP-seq:(Medium) rs1422254521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111 102270 RMVar_ID_102270 Human_SNP_ID_577340203 m1A Human chr15 - 51971714 51971714 51971714 AATGGCGGATATGGAGGATCTCTTCGGGAGCGACGCCGACAGCGAAGCTGAGCGTAAAGGTGGGT AATGGCGGATATGGAGGATCTCTTCGGGAGCGGCGCCGACAGCGAAGCTGAGCGTAAAGGTGGGT T C LEO1 Ensembl:ENSG00000166477 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:51966374..51971733 26863196 MeRIP-seq:(Medium) rs148432881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759822,Human_RBP_ID_4345473,Human_RBP_ID_9370900,Human_RBP_ID_19067232,Human_RBP_ID_26327553,Human_RBP_ID_27810331 Human_Splice_Rec_1602917,Human_Splice_Rec_1602939 102271 RMVar_ID_102271 Human_SNP_ID_577340214 m1A Human chr15 - 51971729 51971729 51971729 GCGGACGTGAGCGATAATGGCGGATATGGAGGATCTCTTCGGGAGCGACGCCGACAGCGAAGCTG GCGGACGTGAGCGATAATGGCGGATATGGAGGCTCTCTTCGGGAGCGACGCCGACAGCGAAGCTG T G LEO1 Ensembl:ENSG00000166477 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:51971627..51971731 26863196 MeRIP-seq:(Medium) rs765851124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_458986,Human_RBP_ID_759822,Human_RBP_ID_8800577,Human_RBP_ID_9370900,Human_RBP_ID_19067232,Human_RBP_ID_27810331 Human_Splice_Rec_1602917,Human_Splice_Rec_1602939 102272 RMVar_ID_102272 Human_SNP_ID_577353175 m1A Human chr15 - 52018856 52018856 52018856 GGCCTCAGTCTCCAGGAAGGGTGGACCTTAAGATGGATTGGCTGGAAGGCGACAGCCCGAGCACA GGCCTCAGTCTCCAGGAAGGGTGGACCTTAAGGTGGATTGGCTGGAAGGCGACAGCCCGAGCACA T C MAPK6-DT Ensembl:ENSG00000259438 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:52018806..52018903 26863196 MeRIP-seq:(Medium) rs146175320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5570442 102273 RMVar_ID_102273 Human_SNP_ID_577353451 m1A Human chr15 - 52019356 52019356 52019356 ACACACACTCACGGGACTTCTCCGACTCATCGAGAGAGTGCGGGGCTCGCGGACTGCCCCCAGTG ACACACACTCACGGGACTTCTCCGACTCATCGGGAGAGTGCGGGGCTCGCGGACTGCCCCCAGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:52019253..52019400 26863196 MeRIP-seq:(Medium) rs1214057697 Functional Loss SNV dbSNP153 33..33 33 - - - 102274 RMVar_ID_102274 Human_SNP_ID_577353497 m1A Human chr15 + 52019468 52019450 52019468 CGGCGGGCCCGGCGGCGGCGGCGGCGGCGGCGACGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT CGGCGGGCCCGGCGG__________________CGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT GCGGCGGCGGCGGCGGCGA G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:52019245..52019469 26863196 MeRIP-seq:(Medium) rs914771413 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_887334,Human_RBP_ID_18458192,Human_RBP_ID_18480904,Human_RBP_ID_26778664 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 102275 RMVar_ID_102275 Human_SNP_ID_577353503 m1A Human chr15 + 52019468 52019456 52019468 CGGCGGGCCCGGCGGCGGCGGCGGCGGCGGCGACGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT CGGCGGGCCCGGCGGCGGCGG____________CGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT GCGGCGGCGGCGA G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:52019245..52019469 26863196 MeRIP-seq:(Medium) rs1283734611 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_887334,Human_RBP_ID_18458192,Human_RBP_ID_18480904,Human_RBP_ID_26778664 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 102276 RMVar_ID_102276 Human_SNP_ID_577353506 m1A Human chr15 + 52019468 52019459 52019468 CGGCGGGCCCGGCGGCGGCGGCGGCGGCGGCGACGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT CGGCGGGCCCGGCGGCGGCGGCGG_________CGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT GCGGCGGCGA G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:52019245..52019469 26863196 MeRIP-seq:(Medium) rs1555396915 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_887334,Human_RBP_ID_18458192,Human_RBP_ID_18480904,Human_RBP_ID_26778664 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 102277 RMVar_ID_102277 Human_SNP_ID_577353515 m1A Human chr15 + 52019468 52019468 52019468 CGGCGGGCCCGGCGGCGGCGGCGGCGGCGGCGACGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT CGGCGGGCCCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGAGCCGGCTCCCTCCTCCATTGTGTGT A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:52019245..52019469 26863196 MeRIP-seq:(Medium) rs1479651542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887334,Human_RBP_ID_18458192,Human_RBP_ID_18480904,Human_RBP_ID_26778664 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 102278 RMVar_ID_102278 Human_SNP_ID_577367772 m1A Human chr15 - 52064789 52064789 52064789 TCAGAAATCCTTCCTCATGTCCTCTCTCCCCAAGCTTCCCATCCTCTACTGGCTCAGTTTCTAGC TCAGAAATCCTTCCTCATGTCCTCTCTCCCCAGGCTTCCCATCCTCTACTGGCTCAGTTTCTAGC T C AC023906.5 Ensembl:ENSG00000259712 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:52064738..52064905 26863196 MeRIP-seq:(Medium) rs1370511392 Functional Loss SNV dbSNP153 33..33 33 - - - 102279 RMVar_ID_102279 Human_SNP_ID_577377155 m1A Human chr15 + 52095590 52095590 52095590 CTACCATTTAATTAAGAAAGCAGTTGCTGTTCAAAAGCATCTTGAGAGGAACAGAAAGGATAAGA CTACCATTTAATTAAGAAAGCAGTTGCTGTTCGAAAGCATCTTGAGAGGAACAGAAAGGATAAGA A G AC023906.1 Ensembl:ENSG00000242327 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878937830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853133,Human_miRNA_ID_1886516,Human_miRNA_ID_1886953 102280 RMVar_ID_102280 Human_SNP_ID_577389675 m1A Human chr15 + 52139646 52139646 52139646 TGAAGCACGCAGAAATTCAAACGCTGTCTAGGATCACCAGCTAGAACACAGCGGAGCCAAGATCC TGAAGCACGCAGAAATTCAAACGCTGTCTAGGGTCACCAGCTAGAACACAGCGGAGCCAAGATCC A G AC023906.4 Ensembl:ENSG00000259709 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52139642..52139744 26863196 MeRIP-seq:(Medium) rs986186773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1603140 102281 RMVar_ID_102281 Human_SNP_ID_577400131 m1A Human chr15 - 52179705 52179696 52179705 AGCCGGACCGGCTCGCCACTTCCCGGGCGGGGACGGCGGGGGCGGTGGGGGCGGTCGTGGCTGCG AGCCGGACCGGCTCGCCACTTCCCGGGCGGGG_________GCGGTGGGGGCGGTCGTGGCTGCG CCCCCGCCGT C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52179698..52179946 26863196 MeRIP-seq:(Medium) rs1232465407 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_5354961 RMVar_hsa_circ_114898,RMVar_hsa_circ_172134 102282 RMVar_ID_102282 Human_SNP_ID_577400137 m1A Human chr15 - 52179705 52179705 52179705 AGCCGGACCGGCTCGCCACTTCCCGGGCGGGGACGGCGGGGGCGGTGGGGGCGGTCGTGGCTGCG AGCCGGACCGGCTCGCCACTTCCCGGGCGGGGGCGGCGGGGGCGGTGGGGGCGGTCGTGGCTGCG T C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52179698..52179946 26863196 MeRIP-seq:(Medium) rs1033291614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5354961 RMVar_hsa_circ_114898,RMVar_hsa_circ_172134 102283 RMVar_ID_102283 Human_SNP_ID_577400221 m1A Human chr15 - 52179873 52179873 52179873 CCTCTCCGCTGCGTCCCCGCGCGAAGATGGCAACCGAGGGGCTGCACGAGAACGAGACGCTGGCG CCTCTCCGCTGCGTCCCCGCGCGAAGATGGCAGCCGAGGGGCTGCACGAGAACGAGACGCTGGCG T C GNB5 Ensembl:ENSG00000069966 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:52179706..52179952 26863196 MeRIP-seq:(Medium) rs1253337393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343110 Human_Splice_Rec_1603008,Human_Splice_Rec_1603122 RMVar_hsa_circ_114898,RMVar_hsa_circ_172134 102284 RMVar_ID_102284 Human_SNP_ID_577406014 m1A Human chr15 - 52203761 52203761 52203761 GAAGAGTAGTGGGGGGCTGAGTAGAGGTGGAAATGGTTAATGGGTACAAAAAAAAGAGAGAAAGA GAAGAGTAGTGGGGGGCTGAGTAGAGGTGGAAGTGGTTAATGGGTACAAAAAAAAGAGAGAAAGA T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52203726..52203846 26863196 MeRIP-seq:(Medium) rs1481693776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266282 102285 RMVar_ID_102285 Human_SNP_ID_577412232 m1A Human chr15 - 52229533 52229533 52229533 TGCAGCCTGGACCTCCTGGGCTCAAGCGATTCATCCACCTCAGCCTCCTGGGTAGCTGGGACTAC TGCAGCCTGGACCTCCTGGGCTCAAGCGATTCCTCCACCTCAGCCTCCTGGGTAGCTGGGACTAC T G MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:52229521..52229603 26863410 MeRIP-seq:(Medium) rs930855060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1548,RMVar_hsa_circ_119455,RMVar_hsa_circ_70197,RMVar_hsa_circ_172140,RMVar_hsa_circ_104965,RMVar_hsa_circ_172142,RMVar_hsa_circ_377041,RMVar_hsa_circ_362306,RMVar_hsa_circ_267082,RMVar_hsa_circ_172143,RMVar_hsa_circ_312009,RMVar_hsa_circ_56659,RMVar_hsa_circ_368006 102286 RMVar_ID_102286 Human_SNP_ID_577426062 m1A Human chr15 - 52282218 52282218 52282218 GGAGGGAGTGTGGCAGGGACAAGAAGACATGGACACCCAGCTTTGTGTGACATTATGAGGTGCCT GGAGGGAGTGTGGCAGGGACAAGAAGACATGGGCACCCAGCTTTGTGTGACATTATGAGGTGCCT T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52282193..52282318 26863196 MeRIP-seq:(Medium) rs1265284805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2887,RMVar_hsa_circ_43267,RMVar_hsa_circ_297640,RMVar_hsa_circ_172146,RMVar_hsa_circ_358234,RMVar_hsa_circ_363711 102287 RMVar_ID_102287 Human_SNP_ID_577428066 m1A Human chr15 + 52288747 52288747 52288747 CTCCAGAATATGGGGCCTTCCCATGAGGCAGGAGTCTGTGGACTGGGATGGAACAGCTCGCCAAG CTCCAGAATATGGGGCCTTCCCATGAGGCAGGGGTCTGTGGACTGGGATGGAACAGCTCGCCAAG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:52288465..52288758 26863196 MeRIP-seq:(Medium) rs950079251 Functional Loss SNV dbSNP153 33..33 33 - - - 102288 RMVar_ID_102288 Human_SNP_ID_577428211 m1A Human chr15 - 52289234 52289234 52289234 TGGGTGGAACTCTCCAGAAACAGCCTATCATGAGAAGAGGCTGGGAAGGACCTTGGGAGACACGG TGGGTGGAACTCTCCAGAAACAGCCTATCATGGGAAGAGGCTGGGAAGGACCTTGGGAGACACGG T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52289106..52289384 26863196 MeRIP-seq:(Medium) rs1329117012 Functional Loss SNV dbSNP153 33..33 33 - - - 102289 RMVar_ID_102289 Human_SNP_ID_577428212 m1A Human chr15 - 52289237 52289237 52289237 AATTGGGTGGAACTCTCCAGAAACAGCCTATCATGAGAAGAGGCTGGGAAGGACCTTGGGAGACA AATTGGGTGGAACTCTCCAGAAACAGCCTATCGTGAGAAGAGGCTGGGAAGGACCTTGGGAGACA T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52289194..52289617 26863196 MeRIP-seq:(Medium) rs937203667 Functional Loss SNV dbSNP153 33..33 33 - - - 102290 RMVar_ID_102290 Human_SNP_ID_577428374 m1A Human chr15 - 52289924 52289924 52289924 GCTAGGGTGGAAGGAACAGAAGTACACAGCAGAAAGCCAAAGAAGGCCTGCCATGTTCCAGAAAG GCTAGGGTGGAAGGAACAGAAGTACACAGCAGTAAGCCAAAGAAGGCCTGCCATGTTCCAGAAAG T A MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52289921..52289991 26863196 MeRIP-seq:(Medium) rs1464551677 Functional Loss SNV dbSNP153 33..33 33 - - - 102291 RMVar_ID_102291 Human_SNP_ID_577428724 m1A Human chr15 - 52291438 52291438 52291438 ATGGGTTAACCTCAGAAAGGAGTGAGGGCCTGAGGCCACAGTGGCAGGAGTTGAAGGCACAGAGA ATGGGTTAACCTCAGAAAGGAGTGAGGGCCTGTGGCCACAGTGGCAGGAGTTGAAGGCACAGAGA T A MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52291318..52291540 26863196 MeRIP-seq:(Medium) rs1392873346 Functional Loss SNV dbSNP153 33..33 33 - - - 102292 RMVar_ID_102292 Human_SNP_ID_577428725 m1A Human chr15 - 52291438 52291438 52291438 ATGGGTTAACCTCAGAAAGGAGTGAGGGCCTGAGGCCACAGTGGCAGGAGTTGAAGGCACAGAGA ATGGGTTAACCTCAGAAAGGAGTGAGGGCCTGGGGCCACAGTGGCAGGAGTTGAAGGCACAGAGA T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52291318..52291540 26863196 MeRIP-seq:(Medium) rs1392873346 Functional Loss SNV dbSNP153 33..33 33 - - - 102293 RMVar_ID_102293 Human_SNP_ID_577429298 m1A Human chr15 - 52293236 52293234 52293236 CTGAGATGGAGCCATCCAGAGGAGGAGCTAACAGGGGAGCTGGAAGCCACCCTGTGGGAACAGGG CTGAGATGGAGCCATCCAGAGGAGGAGCTAAC__GGGAGCTGGAAGCCACCCTGTGGGAACAGGG CCT C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:52293186..52293281 26863196 MeRIP-seq:(Medium) rs1388543835 Functional Loss DEL dbSNP153 33..34 33 - - - 102294 RMVar_ID_102294 Human_SNP_ID_577429322 m1A Human chr15 - 52293317 52293317 52293317 GGAGAAGGCAGACAGAGAAGAGGGTGAGGGACAGGCCAGCGGGGAATGCATCTGTGCAAGGAGTG GGAGAAGGCAGACAGAGAAGAGGGTGAGGGACGGGCCAGCGGGGAATGCATCTGTGCAAGGAGTG T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:52293267..52293835 26863196 MeRIP-seq:(Medium) rs1204192999 Functional Loss SNV dbSNP153 33..33 33 - - - 102295 RMVar_ID_102295 Human_SNP_ID_577429938 m1A Human chr15 + 52295706 52295706 52295706 CGTGCGAGGCTCGGGGGCTGGGCCTGCGCCGCAGAGGCCGGGCGCAGGAGAGACCGCCGCGGAAA CGTGCGAGGCTCGGGGGCTGGGCCTGCGCCGCGGAGGCCGGGCGCAGGAGAGACCGCCGCGGAAA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:52295631..52295732 26863410 MeRIP-seq:(Medium) rs1204304595 Functional Loss SNV dbSNP153 33..33 33 - - - 102296 RMVar_ID_102296 Human_SNP_ID_577487163 m1A Human chr15 + 52528935 52528935 52528935 CAGGGAGCAGGGCAGGGCAGGGCCGGGCGGGGAGGGCCGCGCGGGGCGGGGCGGGGCGGGGCGCC CAGGGAGCAGGGCAGGGCAGGGCCGGGCGGGGGGGGCCGCGCGGGGCGGGGCGGGGCGGGGCGCC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr15:52528837..52529082;chr15:52528878..52528963 26863410 MeRIP-seq:(Medium) rs1221035362 Functional Loss SNV dbSNP153 33..33 33 - - - 102297 RMVar_ID_102297 Human_SNP_ID_577487202 m1A Human chr15 + 52529023 52529013 52529023 GCCTCGCCATCACTCCCGGGCTCGCCGCGAGCAGCCGCGAGCGCTCCACCTGCCCGGGGTCCTAG GCCTCGCCATCACTCCCGGGCTC__________GCCGCGAGCGCTCCACCTGCCCGGGGTCCTAG CGCCGCGAGCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52528984..52529111 26863196 MeRIP-seq:(Medium) rs1023662502 Functional Loss DEL dbSNP153 24..33 33 - - - 102298 RMVar_ID_102298 Human_SNP_ID_577487207 m1A Human chr15 + 52529023 52529023 52529023 GCCTCGCCATCACTCCCGGGCTCGCCGCGAGCAGCCGCGAGCGCTCCACCTGCCCGGGGTCCTAG GCCTCGCCATCACTCCCGGGCTCGCCGCGAGCCGCCGCGAGCGCTCCACCTGCCCGGGGTCCTAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52528984..52529111 26863196 MeRIP-seq:(Medium) rs1238999228 Functional Loss SNV dbSNP153 33..33 33 - - - 102299 RMVar_ID_102299 Human_SNP_ID_577497773 m1A Human chr15 - 52568881 52568881 52568881 CTCGTCTGCAGAGGGAGCACTATGTCTGCGGAAGTCCCCGAGGCAGCCTCCGCGGAGGAGCAGAA CTCGTCTGCAGAGGGAGCACTATGTCTGCGGAGGTCCCCGAGGCAGCCTCCGCGGAGGAGCAGAA T C ARPP19 Ensembl:ENSG00000128989 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:52568876..52569006 26863196 MeRIP-seq:(Medium) rs774444622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4906,Human_RBP_ID_459242,Human_RBP_ID_758826,Human_RBP_ID_814739,Human_RBP_ID_1505549,Human_RBP_ID_4342288,Human_RBP_ID_5141614,Human_RBP_ID_5354012,Human_RBP_ID_9324273,Human_RBP_ID_17862139,Human_RBP_ID_18436524,Human_RBP_ID_22047487,Human_RBP_ID_22580687,Human_RBP_ID_22798906,Human_RBP_ID_24544213 Human_Splice_Rec_1603966,Human_Splice_Rec_1603967,Human_Splice_Rec_1603971,Human_Splice_Rec_1603986,Human_Splice_Rec_1603987,Human_Splice_Rec_1603992,Human_Splice_Rec_1603993,Human_Splice_Rec_1603996,Human_Splice_Rec_1603997,Human_Splice_Rec_1604001,Human_Splice_Rec_1604016,Human_Splice_Rec_1604017 Human_miRNA_ID_2715305,Human_miRNA_ID_3051284 RMVar_hsa_circ_125363,RMVar_hsa_circ_172185,RMVar_hsa_circ_76522,RMVar_hsa_circ_172184 102300 RMVar_ID_102300 Human_SNP_ID_577497847 m1A Human chr15 + 52568981 52568981 52568981 GCCACCCGGCCGCCGCCCGTCCCAGCTCTCCCAGGGCCCGCCGGGCCGCCTCCGCCCGCGAAAAT GCCACCCGGCCGCCGCCCGTCCCAGCTCTCCCGGGGCCCGCCGGGCCGCCTCCGCCCGCGAAAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:52568804..52569200;chr15:52568794..52569200 26863196 MeRIP-seq:(Medium) rs1426052424 Functional Loss SNV dbSNP153 33..33 33 - - - 102301 RMVar_ID_102301 Human_SNP_ID_577524978 m1A Human chr15 - 52678768 52678767 52678768 GCCGCGGCGGGACGGAAGGGGTTGTGCAGAGCAGGGGGCGAGCACAGGCTGTAAACACCTCCCCC GCCGCGGCGGGACGGAAGGGGTTGTGCAGAGC_GGGGGCGAGCACAGGCTGTAAACACCTCCCCC CT C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:52678751..52678888 26863196 MeRIP-seq:(Medium) rs1275703370 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_814541,Human_RBP_ID_3489617,Human_RBP_ID_9353039 Human_Splice_Rec_1604131,Human_Splice_Rec_1604167 102302 RMVar_ID_102302 Human_SNP_ID_578205556 m1A Human chr15 - 55192827 55192827 55192827 TCTCAATATTTTAACTTTTCTTGTAGGTGTTCAGATTTTGCAAATCTAAATGTCATAAAAACTTT TCTCAATATTTTAACTTTTCTTGTAGGTGTTCGGATTTTGCAAATCTAAATGTCATAAAAACTTT T C RSL24D1 Ensembl:ENSG00000137876 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:55192776..55192850 32194978 MeRIP-seq:(Medium) rs17851202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9345235,Human_RBP_ID_22439796,Human_RBP_ID_25145874 Human_Splice_Rec_1604672,Human_Splice_Rec_1604682,Human_Splice_Rec_1604692,Human_Splice_Rec_1604696,Human_Splice_Rec_1604706,Human_Splice_Rec_1604710 Human_miRNA_ID_2645690 RMVar_hsa_circ_93492,RMVar_hsa_circ_110642,RMVar_hsa_circ_172234,RMVar_hsa_circ_172235 102303 RMVar_ID_102303 Human_SNP_ID_578208979 m1A Human chr15 - 55205547 55205547 55205547 GGTGCGATCAAATGGTCATGCCTCTACGGATCAGTTAAGTGAAGAAAAGGAGAAAGGGGCATGTG GGTGCGATCAAATGGTCATGCCTCTACGGATCGGTTAAGTGAAGAAAAGGAGAAAGGGGCATGTG T C RAB27A Ensembl:ENSG00000069974 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:55205383..55205563 32194978 MeRIP-seq:(Medium) rs761321376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17862328,Human_RBP_ID_23656007 102304 RMVar_ID_102304 Human_SNP_ID_578231417 m1A Human chr15 + 55289772 55289766 55289772 CCGCCTGGCTCGGGTCCTCGCGCGCCGCGTCCACCCGCCGCCGGCCTTTTTTGGGTCGTTGGCGG CCGCCTGGCTCGGGTCCTCGCGCGCCG______CCCGCCGCCGGCCTTTTTTGGGTCGTTGGCGG GCGTCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:55289651..55289789;chr15:55289537..55289800 26863196 MeRIP-seq:(Medium) rs1031349098 Functional Loss DEL dbSNP153 28..33 33 - - - 102305 RMVar_ID_102305 Human_SNP_ID_578240265 m1A Human chr15 + 55319308 55319308 55319308 GAATGGAGCCGGGGGGCGGAGATGCCAGCCTCACTTTGCATGGTCTCCAGAACCGCTCCCACGGC GAATGGAGCCGGGGGGCGGAGATGCCAGCCTCGCTTTGCATGGTCTCCAGAACCGCTCCCACGGC A G PIGB Ensembl:ENSG00000069943 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:55319258..55319359 26863196 MeRIP-seq:(Medium) rs765467670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2715306,Human_miRNA_ID_2793264,Human_miRNA_ID_2846455,Human_miRNA_ID_2849476,Human_miRNA_ID_3051285 RMVar_hsa_circ_95535,RMVar_hsa_circ_172240 102306 RMVar_ID_102306 Human_SNP_ID_578305074 m1A Human chr15 - 55548997 55548997 55548997 GTGGGAAATATTACCTGAATTTTTTTTTTTTTAGGTGGTGATAGTGGACTGGATGGGTTAGGAGG GTGGGAAATATTACCTGAATTTTTTTTTTTTTTGGTGGTGATAGTGGACTGGATGGGTTAGGAGG T A PYGO1 Ensembl:ENSG00000171016 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:55548970..55549035 26863196 MeRIP-seq:(Medium) rs867413175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4325642 Human_Splice_Rec_1605187,Human_Splice_Rec_1605191,Human_Splice_Rec_1605197 102307 RMVar_ID_102307 Human_SNP_ID_578328209 m1A Human chr15 - 55632548 55632548 55632548 GGGAAGAGCAGGCAGTAAGAAATGAAGTAGGGAGGTAACTAAGGGCAGATGTAGACCAGATTTCA GGGAAGAGCAGGCAGTAAGAAATGAAGTAGGGGGGTAACTAAGGGCAGATGTAGACCAGATTTCA T C PRTG Ensembl:ENSG00000166450 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:55632545..55632655 26863196 MeRIP-seq:(Medium) rs1302130575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2919,RMVar_hsa_circ_4547,RMVar_hsa_circ_114554,RMVar_hsa_circ_348337,RMVar_hsa_circ_172270,RMVar_hsa_circ_172271 102308 RMVar_ID_102308 Human_SNP_ID_578383608 m1A Human chr15 - 55835687 55835687 55835687 GGAGTTGAGATAGGATTGGTAAGGGAATGAAGATAGTGGTGGTGTTCAGAGCTGCATGTGCATTT GGAGTTGAGATAGGATTGGTAAGGGAATGAAGGTAGTGGTGGTGTTCAGAGCTGCATGTGCATTT T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:55835637..55835775 26863196 MeRIP-seq:(Medium) rs1268036654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23656432 RMVar_hsa_circ_3239,RMVar_hsa_circ_79392,RMVar_hsa_circ_172275,RMVar_hsa_circ_67806,RMVar_hsa_circ_51192,RMVar_hsa_circ_55562 102309 RMVar_ID_102309 Human_SNP_ID_578424259 m1A Human chr15 - 55993314 55993314 55993314 GGCTCGGCGCGCGGGCGCTGGGGGCTCGCTGGAGGGAGCAAGCTTGTCGGGTCCACACCCGCCCC GGCTCGGCGCGCGGGCGCTGGGGGCTCGCTGGGGGGAGCAAGCTTGTCGGGTCCACACCCGCCCC T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:55993307..55993540 26863196 MeRIP-seq:(Medium) rs1482154545 Functional Loss SNV dbSNP153 33..33 33 - - - 102310 RMVar_ID_102310 Human_SNP_ID_578424505 m1A Human chr15 + 55993832 55993832 55993832 GTGGGGAGGGCGTGCGGCGGGGCTCGGGTGGGATGAGCGCGCGCGGCGGGGACCATGGCGTGGGG GTGGGGAGGGCGTGCGGCGGGGCTCGGGTGGGGTGAGCGCGCGCGGCGGGGACCATGGCGTGGGG A G lnc-TEX9-6,lnc-TEX9-6:2,lnc-TEX9-6:3,lnc-TEX9-6:4,lnc-TEX9-6:5 RNACentral:URS0000D5B96D,RNACentral:URS0000D5C4BE,RNACentral:URS0000D5C656,RNACentral:URS0000D5C069,RNACentral:URS0000D56D4B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:55993781..55993957;chr15:55993791..55994065 26863196 MeRIP-seq:(Medium) rs1450562926 Functional Loss SNV dbSNP153 33..33 33 - - - 102311 RMVar_ID_102311 Human_SNP_ID_578424514 m1A Human chr15 - 55993860 55993860 55993860 ACCGAGGGCGCGCCCCGCCACGCGCGCTCCCCACGCCATGGTCCCCGCCGCGCGCGCTCATCCCA ACCGAGGGCGCGCCCCGCCACGCGCGCTCCCCCCGCCATGGTCCCCGCCGCGCGCGCTCATCCCA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:55993813..55993945 26863196 MeRIP-seq:(Medium) rs1428981142 Functional Loss SNV dbSNP153 33..33 33 - - - 102312 RMVar_ID_102312 Human_SNP_ID_578430883 m1A Human chr15 + 56019372 56019372 56019372 GTTTTCTAACTTTCATCTTTTTCCCATGCTGGATGCTTCCTGCCGTTGGACATCAGACTCCAGGT GTTTTCTAACTTTCATCTTTTTCCCATGCTGGCTGCTTCCTGCCGTTGGACATCAGACTCCAGGT A C lnc-TEX9-6,lnc-TEX9-6:2,lnc-TEX9-6:3,lnc-TEX9-6:4,lnc-TEX9-6:5,lnc-TEX9-6:6,lnc-TEX9-6:7,lnc-TEX9-6:8,lnc-TEX9-6:9 RNACentral:URS0000D5B96D,RNACentral:URS0000D5C656,RNACentral:URS0000D5C4BE,RNACentral:URS0000D5AAA5,RNACentral:URS0000D5C069,RNACentral:URS0000D56F7A,RNACentral:URS0000D56E7A,RNACentral:URS0000D57BB3,RNACentral:URS0000D5765A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:56019321..56019457 26863196 MeRIP-seq:(Medium) rs948495018 Functional Loss SNV dbSNP153 33..33 33 - - - 102313 RMVar_ID_102313 Human_SNP_ID_578490533 m1A Human chr15 + 56243668 56243668 56243668 GAAGTGGGGGGGGCAGGCTCCCCCCAAAATCCAAGAAGAACGGTTGCTCAGGGATTTGGCGGCCA GAAGTGGGGGGGGCAGGCTCCCCCCAAAATCCCAGAAGAACGGTTGCTCAGGGATTTGGCGGCCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:56243587..56243732 26863196 MeRIP-seq:(Medium) rs1350971924 Functional Loss SNV dbSNP153 33..33 33 - - - 102314 RMVar_ID_102314 Human_SNP_ID_578490601 m1A Human chr15 - 56243807 56243807 56243807 CGGCGGCCGCGGCGGCGGCGGGGCCGGGAGCGAGCGGCGGCGGCGGCGGCGGCGTGGGGAGTGGC CGGCGGCCGCGGCGGCGGCGGGGCCGGGAGCGGGCGGCGGCGGCGGCGGCGGCGTGGGGAGTGGC T C RFX7 Ensembl:ENSG00000181827 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:56243651..56243870 26863196 MeRIP-seq:(Medium) rs1210081813 Functional Loss SNV dbSNP153 33..33 33 - - - 102315 RMVar_ID_102315 Human_SNP_ID_578548350 m1A Human chr15 - 56464249 56464249 56464249 CAAAATATGCATCTTTTTTTTTCTTCCATCGTAGGGTTCCAAAAGGAGAAATTTGAGCTGTAGTG CAAAATATGCATCTTTTTTTTTCTTCCATCGTGGGGTTCCAAAAGGAGAAATTTGAGCTGTAGTG T C MNS1 Ensembl:ENSG00000138587 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:56464132..56464275 26863196 MeRIP-seq:(Medium) rs1300747054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172314 102316 RMVar_ID_102316 Human_SNP_ID_578548558 m1A Human chr15 - 56464924 56464924 56464924 GGGACTTGAAACTACTTGTTTATTGTTGATTTAATTCTAGTTTGGCGCTCATCTGCTTCTAAAAA GGGACTTGAAACTACTTGTTTATTGTTGATTTCATTCTAGTTTGGCGCTCATCTGCTTCTAAAAA T G MNS1 Ensembl:ENSG00000138587 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:56464922..56465115 26863196 MeRIP-seq:(Medium) rs764511040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172314 102317 RMVar_ID_102317 Human_SNP_ID_578548612 m1A Human chr15 + 56465017 56465017 56465017 AAAATACCCCCTCTCGTGGGACCGCGGCCACCACCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC AAAATACCCCCTCTCGTGGGACCGCGGCCACCCCCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:56464927..56465075 26863196 MeRIP-seq:(Medium) rs755806825 Functional Loss SNV dbSNP153 33..33 33 - - - 102318 RMVar_ID_102318 Human_SNP_ID_578548613 m1A Human chr15 + 56465017 56465017 56465017 AAAATACCCCCTCTCGTGGGACCGCGGCCACCACCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC AAAATACCCCCTCTCGTGGGACCGCGGCCACCGCCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:56464927..56465075 26863196 MeRIP-seq:(Medium) rs755806825 Functional Loss SNV dbSNP153 33..33 33 - - - 102319 RMVar_ID_102319 Human_SNP_ID_578619145 m1A Human chr15 + 56733529 56733529 56733529 GGAGGAGAAAGAGGAGGAGGAAAAGGAGGAGCACGAAAAACTACACTGCGGCGACGGCGGCGGCT GGAGGAGAAAGAGGAGGAGGAAAAGGAGGAGCCCGAAAAACTACACTGCGGCGACGGCGGCGGCT A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:56733524..56733606 26863410 MeRIP-seq:(Medium) rs1379192569 Functional Loss SNV dbSNP153 33..33 33 - - - 102320 RMVar_ID_102320 Human_SNP_ID_578663859 m1A Human chr15 + 56918366 56918366 56918366 GACCAACGCGAGGAGGCGCCACGGTACCTGCCACCCCGCTCCCAGGAGGCCCGGACGAGGCTTCG GACCAACGCGAGGAGGCGCCACGGTACCTGCCCCCCCGCTCCCAGGAGGCCCGGACGAGGCTTCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:56918318..56918474 26863196 MeRIP-seq:(Medium) rs1429180160 Functional Loss SNV dbSNP153 33..33 33 - - - 102321 RMVar_ID_102321 Human_SNP_ID_578663860 m1A Human chr15 + 56918366 56918366 56918366 GACCAACGCGAGGAGGCGCCACGGTACCTGCCACCCCGCTCCCAGGAGGCCCGGACGAGGCTTCG GACCAACGCGAGGAGGCGCCACGGTACCTGCCTCCCCGCTCCCAGGAGGCCCGGACGAGGCTTCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:56918318..56918474 26863196 MeRIP-seq:(Medium) rs1429180160 Functional Loss SNV dbSNP153 33..33 33 - - - 102322 RMVar_ID_102322 Human_SNP_ID_578753022 m1A Human chr15 + 57239662 57239662 57239662 GAGTAAAGATTTAAAGTGGTGTCATGGCAGTGATTATGACATGTGCCTGTCCCAGAAACATTAGA GAGTAAAGATTTAAAGTGGTGTCATGGCAGTGGTTATGACATGTGCCTGTCCCAGAAACATTAGA A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:57239651..57239719 26863196 MeRIP-seq:(Medium) rs1394862318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_342551,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172357,RMVar_hsa_circ_60015,RMVar_hsa_circ_366681,RMVar_hsa_circ_325426,RMVar_hsa_circ_19302,RMVar_hsa_circ_62833,RMVar_hsa_circ_172365,RMVar_hsa_circ_111968,RMVar_hsa_circ_290673,RMVar_hsa_circ_328340,RMVar_hsa_circ_335020,RMVar_hsa_circ_68985,RMVar_hsa_circ_81714,RMVar_hsa_circ_58488,RMVar_hsa_circ_15060,RMVar_hsa_circ_172366,RMVar_hsa_circ_172368,RMVar_hsa_circ_172370,RMVar_hsa_circ_172369,RMVar_hsa_circ_172367,RMVar_hsa_circ_102459,RMVar_hsa_circ_350936,RMVar_hsa_circ_172372,RMVar_hsa_circ_47522,RMVar_hsa_circ_359055,RMVar_hsa_circ_339994,RMVar_hsa_circ_333565 102323 RMVar_ID_102323 Human_SNP_ID_578764944 m1A Human chr15 + 57282402 57282402 57282402 CAGCAATTTGTTCAGCTTGAGACCTAATTCATAACTTAAAACCATAGTGATAAAAATTCTTTCCC CAGCAATTTGTTCAGCTTGAGACCTAATTCATGACTTAAAACCATAGTGATAAAAATTCTTTCCC A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:57282399..57282532 26863196 MeRIP-seq:(Medium) rs1260177298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338431,RMVar_hsa_circ_172377,RMVar_hsa_circ_377263 102324 RMVar_ID_102324 Human_SNP_ID_578808626 m1A Human chr15 - 57438029 57438029 57438029 AGTCTCAGATGGACCCCATATTCCTGCTGCACATGTTGATATTCACCGAAATACAGCTCCATGGT AGTCTCAGATGGACCCCATATTCCTGCTGCACGTGTTGATATTCACCGAAATACAGCTCCATGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:57438008..57438073 26863196 MeRIP-seq:(Medium) rs372675578 Functional Loss SNV dbSNP153 33..33 33 - - - 102325 RMVar_ID_102325 Human_SNP_ID_578815597 m1A Human chr15 - 57461801 57461801 57461801 TCAGCTTGTCCATCTCCTGATCATGGCTGGAAACCTCTTCTTTCAGGGCTCCCTTCAGGGCGGTG TCAGCTTGTCCATCTCCTGATCATGGCTGGAAGCCTCTTCTTTCAGGGCTCCCTTCAGGGCGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:57461753..57461824 26863196 MeRIP-seq:(Medium) rs1195128931 Functional Loss SNV dbSNP153 33..33 33 - - - 102326 RMVar_ID_102326 Human_SNP_ID_578851340 m1A Human chr15 - 57591983 57591983 57591983 GCGGGCTGGACGCCGGCGTTCCTCCCGGGCAGAATAAGCGTGCGGGGCCCGCCCTGCGCGGGGGC GCGGGCTGGACGCCGGCGTTCCTCCCGGGCAGGATAAGCGTGCGGGGCCCGCCCTGCGCGGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:57591948..57592054 26863196 MeRIP-seq:(Medium) rs1690328 Functional Loss SNV dbSNP153 33..33 33 - - - 102327 RMVar_ID_102327 Human_SNP_ID_578883625 m1A Human chr15 + 57706807 57706807 57706807 GGCGCTAGTAGCGGGGCCTGCCGAGGAAGCCGAGTGCCCGCCGCCGCGCCAGCCTCAGCCCGCGC GGCGCTAGTAGCGGGGCCTGCCGAGGAAGCCGTGTGCCCGCCGCCGCGCCAGCCTCAGCCCGCGC A T POLR2M,GCOM1 Ensembl:ENSG00000255529,Ensembl:ENSG00000137878 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:57706757..57706831 26863196 MeRIP-seq:(Medium) rs1263775001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342703,Human_RBP_ID_18418367 RMVar_hsa_circ_80333,RMVar_hsa_circ_172390 102328 RMVar_ID_102328 Human_SNP_ID_578883643 m1A Human chr15 - 57706844 57706844 57706844 CTTGGGGCTCGAAGCCGCGGGGCAGCGAGCACATTCTGCGCGGGCTGAGGCTGGCGCGGCGGCGG CTTGGGGCTCGAAGCCGCGGGGCAGCGAGCACGTTCTGCGCGGGCTGAGGCTGGCGCGGCGGCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:57706747..57706928 26863410 MeRIP-seq:(Medium) rs1430671820 Functional Loss SNV dbSNP153 33..33 33 - - - 102329 RMVar_ID_102329 Human_SNP_ID_578989332 m1A Human chr15 - 58065633 58065633 58065633 ACCCGGCCCGCCACCATGACTTCCAGCAAGATAGAGATGCCCGGCGAGGTGAAGGCCGACCCCGC ACCCGGCCCGCCACCATGACTTCCAGCAAGATGGAGATGCCCGGCGAGGTGAAGGCCGACCCCGC T C ALDH1A2 Ensembl:ENSG00000128918 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:58065563..58066830 26863410 MeRIP-seq:(Medium) rs780158113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4326095,Human_RBP_ID_9053973,Human_RBP_ID_22532600 Human_Splice_Rec_1607149,Human_Splice_Rec_1607185,Human_Splice_Rec_1607209,Human_Splice_Rec_1607231,Human_Splice_Rec_1607325 RMVar_hsa_circ_103855,RMVar_hsa_circ_172392 102330 RMVar_ID_102330 Human_SNP_ID_579037906 m1A Human chr15 - 58243195 58243195 58243195 GACACGTGAATAATGCACTTGTGGAATTAATCAGCCTTGTCATTTTGGGCTAGTTGCCATGGCTA GACACGTGAATAATGCACTTGTGGAATTAATCCGCCTTGTCATTTTGGGCTAGTTGCCATGGCTA T G ALDH1A2 Ensembl:ENSG00000128918 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:58243136..58243220 26863410 MeRIP-seq:(Medium) rs771496420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352729 102331 RMVar_ID_102331 Human_SNP_ID_579171965 m1A Human chr15 - 58717729 58717729 58717729 GATACTAATTCAGAATGTTGTTTTTTTTTTATAGGTCAGTATGGGAATCCTTTAAATAAATATAT GATACTAATTCAGAATGTTGTTTTTTTTTTATTGGTCAGTATGGGAATCCTTTAAATAAATATAT T A ADAM10 Ensembl:ENSG00000137845 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:58717708..58717775;chr15:58717694..58717792 26863196 MeRIP-seq:(Medium) rs1397484875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343541 RMVar_hsa_circ_116696,RMVar_hsa_circ_172416 102332 RMVar_ID_102332 Human_SNP_ID_579181128 m1A Human chr15 + 58749585 58749585 58749585 CCGCCGCCGCCTCCTCACGGGTTAACAGCAGCACATCGATCCGGAGGGAGAAGCTGAAGGGGCTT CCGCCGCCGCCTCCTCACGGGTTAACAGCAGCCCATCGATCCGGAGGGAGAAGCTGAAGGGGCTT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:58749558..58749706 26863196 MeRIP-seq:(Medium) rs200342358 Functional Loss SNV dbSNP153 33..33 33 - - - 102333 RMVar_ID_102333 Human_SNP_ID_579187313 m1A Human chr15 - 58771371 58771371 58771371 CTCTCCATACCGGGCCGCCCGCCCCCAGCTCTATGGAGACCGCGGCCACTTCTCCGCAGCCAGCG CTCTCCATACCGGGCCGCCCGCCCCCAGCTCTGTGGAGACCGCGGCCACTTCTCCGCAGCCAGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:58771322..58771588 26863196 MeRIP-seq:(Medium) rs1417822929 Functional Loss SNV dbSNP153 33..33 33 - - - 102334 RMVar_ID_102334 Human_SNP_ID_579219424 m1A Human chr15 - 58883782 58883782 58883782 AGTGACTTTTCATATGCTATTCTTTTAGCACTATCCTGAGGAGCGACATGTGGTTGAACGCCATG AGTGACTTTTCATATGCTATTCTTTTAGCACTGTCCTGAGGAGCGACATGTGGTTGAACGCCATG T C SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:58883626..58883841 26863196 MeRIP-seq:(Medium) rs1437262530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232099,Human_RBP_ID_885589,Human_RBP_ID_2447440,Human_RBP_ID_8803856,Human_RBP_ID_9283652,Human_RBP_ID_9371633,Human_RBP_ID_18982275,Human_RBP_ID_19068257,Human_RBP_ID_24544087,Human_RBP_ID_26326766,Human_RBP_ID_27809606 Human_Splice_Rec_1607918,Human_Splice_Rec_1607942,Human_Splice_Rec_1607946,Human_Splice_Rec_1607984,Human_Splice_Rec_1607988,Human_Splice_Rec_1608024,Human_Splice_Rec_1608032 RMVar_hsa_circ_350062,RMVar_hsa_circ_366512,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_126659,RMVar_hsa_circ_335055,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_63224,RMVar_hsa_circ_73676,RMVar_hsa_circ_172433,RMVar_hsa_circ_172434,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431 102335 RMVar_ID_102335 Human_SNP_ID_579219425 m1A Human chr15 + 58883783 58883783 58883783 ATGGCGTTCAACCACATGTCGCTCCTCAGGATAGTGCTAAAAGAATAGCATATGAAAAGTCACTT ATGGCGTTCAACCACATGTCGCTCCTCAGGATGGTGCTAAAAGAATAGCATATGAAAAGTCACTT A G RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:58883685..58883832 26863196 MeRIP-seq:(Medium) rs939594219 Functional Loss SNV dbSNP153 33..33 33 - - - 102336 RMVar_ID_102336 Human_SNP_ID_579220393 m1A Human chr15 - 58887018 58887018 58887018 TCGTAGCAGCGCTTCGGGGTACGGGAGCAGAGAGGGAGACAGAGGAGTCATCACAGACCGAGGAG TCGTAGCAGCGCTTCGGGGTACGGGAGCAGAGGGGGAGACAGAGGAGTCATCACAGACCGAGGAG T C SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:58886914..58887116 26863196 MeRIP-seq:(Medium) rs866558673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4911,Human_RBP_ID_41613,Human_RBP_ID_815340,Human_RBP_ID_885590,Human_RBP_ID_4326269,Human_RBP_ID_9370964,Human_RBP_ID_22934720,Human_RBP_ID_24544088,Human_RBP_ID_26326769,Human_RBP_ID_27809608 Human_Splice_Rec_1607917,Human_Splice_Rec_1607941,Human_Splice_Rec_1607945,Human_Splice_Rec_1607983,Human_Splice_Rec_1607987,Human_Splice_Rec_1608023,Human_Splice_Rec_1608031 RMVar_hsa_circ_13410,RMVar_hsa_circ_350062,RMVar_hsa_circ_366512,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_126659,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_63224,RMVar_hsa_circ_73676,RMVar_hsa_circ_172433,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431,RMVar_hsa_circ_274564,RMVar_hsa_circ_360905,RMVar_hsa_circ_56300,RMVar_hsa_circ_172435,RMVar_hsa_circ_172436 102337 RMVar_ID_102337 Human_SNP_ID_579220568 m1A Human chr15 - 58887397 58887397 58887397 TGAGCCTCCACCACCAAGAAATGAACTTAGAGAATCAGACAGGCGAGAAGTACGAGGGGAGCGAG TGAGCCTCCACCACCAAGAAATGAACTTAGAGGATCAGACAGGCGAGAAGTACGAGGGGAGCGAG T C SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:58887347..58887475 26863196 MeRIP-seq:(Medium) rs148440197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41616,Human_RBP_ID_2447443,Human_RBP_ID_12539262,Human_RBP_ID_24544089,Human_RBP_ID_26326772,Human_RBP_ID_26932292,Human_RBP_ID_27810373 Human_miRNA_ID_2225557,Human_miRNA_ID_2225558 RMVar_hsa_circ_13410,RMVar_hsa_circ_350062,RMVar_hsa_circ_366512,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_126659,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_63224,RMVar_hsa_circ_73676,RMVar_hsa_circ_172433,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431,RMVar_hsa_circ_274564,RMVar_hsa_circ_360905,RMVar_hsa_circ_56300,RMVar_hsa_circ_172435,RMVar_hsa_circ_172436 102338 RMVar_ID_102338 Human_SNP_ID_579220572 m1A Human chr15 - 58887420 58887420 58887420 AATTTCAGTGACTCCAGAAGAAATGAGCCTCCACCACCAAGAAATGAACTTAGAGAATCAGACAG AATTTCAGTGACTCCAGAAGAAATGAGCCTCCGCCACCAAGAAATGAACTTAGAGAATCAGACAG T C SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:58887370..58887475 26863196 MeRIP-seq:(Medium) rs1363898784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2447444,Human_RBP_ID_18664749,Human_RBP_ID_24544089,Human_RBP_ID_26326773,Human_RBP_ID_27810373 RMVar_hsa_circ_13410,RMVar_hsa_circ_350062,RMVar_hsa_circ_366512,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_126659,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_63224,RMVar_hsa_circ_73676,RMVar_hsa_circ_172433,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431,RMVar_hsa_circ_274564,RMVar_hsa_circ_360905,RMVar_hsa_circ_56300,RMVar_hsa_circ_172435,RMVar_hsa_circ_172436 102339 RMVar_ID_102339 Human_SNP_ID_579221866 m1A Human chr15 - 58893038 58893038 58893038 TTTTCTACAGATTCATGGAAGAAGTAAGGAAAAGGAGAGAGCTAGTCTAGATAAAAAAAGAGATA TTTTCTACAGATTCATGGAAGAAGTAAGGAAAGGGAGAGAGCTAGTCTAGATAAAAAAAGAGATA T C SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:58892858..58893075 26863196 MeRIP-seq:(Medium) rs1172242070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41621,Human_RBP_ID_197568,Human_RBP_ID_1511596,Human_RBP_ID_5523345,Human_RBP_ID_9345244,Human_RBP_ID_18411228,Human_RBP_ID_18664753,Human_RBP_ID_24544091,Human_RBP_ID_26326782,Human_RBP_ID_27809614 Human_Splice_Rec_1607906,Human_Splice_Rec_1607930,Human_Splice_Rec_1607972,Human_Splice_Rec_1608012,Human_Splice_Rec_1608040 RMVar_hsa_circ_13410,RMVar_hsa_circ_350062,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_73676,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431,RMVar_hsa_circ_360905,RMVar_hsa_circ_56300,RMVar_hsa_circ_73568,RMVar_hsa_circ_74124,RMVar_hsa_circ_332737,RMVar_hsa_circ_19220,RMVar_hsa_circ_66919,RMVar_hsa_circ_60212,RMVar_hsa_circ_2860 102340 RMVar_ID_102340 Human_SNP_ID_579223517 m1A Human chr15 - 58899640 58899640 58899640 CATTGCACAGAGCCCGGAGAAGGAAAGCAAGGATTATGAGATGAATGCGAACCATAAAGATGGTA CATTGCACAGAGCCCGGAGAAGGAAAGCAAGGCTTATGAGATGAATGCGAACCATAAAGATGGTA T G SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:58899590..58899687 26863196 MeRIP-seq:(Medium) rs778055292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815343,Human_RBP_ID_12539340 Human_Splice_Rec_1608134 Human_miRNA_ID_2490602,Human_miRNA_ID_2752687 RMVar_hsa_circ_13410,RMVar_hsa_circ_350062,RMVar_hsa_circ_376047,RMVar_hsa_circ_172430,RMVar_hsa_circ_56300,RMVar_hsa_circ_47364,RMVar_hsa_circ_74124,RMVar_hsa_circ_66919,RMVar_hsa_circ_172437,RMVar_hsa_circ_2860,RMVar_hsa_circ_108969,RMVar_hsa_circ_172438,RMVar_hsa_circ_119655,RMVar_hsa_circ_172440,RMVar_hsa_circ_331800,RMVar_hsa_circ_337536,RMVar_hsa_circ_315472,RMVar_hsa_circ_172439,RMVar_hsa_circ_60699 102341 RMVar_ID_102341 Human_SNP_ID_579248138 m1A Human chr15 + 58987735 58987735 58987735 GGCGGCGGCGGCGAAGCGGCGGCGGCGGCTGTAGGGGAGCAGCGGCAGTGGCGGCGACGGCGAGG GGCGGCGGCGGCGAAGCGGCGGCGGCGGCTGTGGGGGAGCAGCGGCAGTGGCGGCGACGGCGAGG A G RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:58987675..58987838;chr15:58987686..58987950;chr15:58987676..58987878 26863196 MeRIP-seq:(Medium) rs1408746645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_814669 RMVar_hsa_circ_93047,RMVar_hsa_circ_172449 102342 RMVar_ID_102342 Human_SNP_ID_579274700 m1A Human chr15 - 59080991 59080991 59080991 GGCGGAGGCTGAGTCTGAGGAGGGGGGTTTCCATGAGAATGCGGGCAGGCAGAAGCTTGATGATG GGCGGAGGCTGAGTCTGAGGAGGGGGGTTTCCGTGAGAATGCGGGCAGGCAGAAGCTTGATGATG T C lnc-SLTM-2 RNACentral:URS00008BC6FB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:59080941..59081075 26863196 MeRIP-seq:(Medium) rs1474717599 Functional Loss SNV dbSNP153 33..33 33 - - - 102343 RMVar_ID_102343 Human_SNP_ID_579281291 m1A Human chr15 + 59105177 59105177 59105177 CGAAGATCCCCAGCGCTGCGGGCTCGGAGAGCAGTCCTAACGGCGCCTCGTACGCTAGTGTCCTC CGAAGATCCCCAGCGCTGCGGGCTCGGAGAGCGGTCCTAACGGCGCCTCGTACGCTAGTGTCCTC A G CCNB2 Ensembl:ENSG00000157456 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:59105126..59105329;chr15:59105126..59105300;chr15:59105126..59105274 26863196 MeRIP-seq:(Medium) rs536497004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4326404,Human_RBP_ID_6442291,Human_RBP_ID_17366903,Human_RBP_ID_22439806 RMVar_hsa_circ_80183,RMVar_hsa_circ_102093,RMVar_hsa_circ_172468,RMVar_hsa_circ_172469 102344 RMVar_ID_102344 Human_SNP_ID_579281292 m1A Human chr15 + 59105177 59105177 59105177 CGAAGATCCCCAGCGCTGCGGGCTCGGAGAGCAGTCCTAACGGCGCCTCGTACGCTAGTGTCCTC CGAAGATCCCCAGCGCTGCGGGCTCGGAGAGCTGTCCTAACGGCGCCTCGTACGCTAGTGTCCTC A T CCNB2 Ensembl:ENSG00000157456 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:59105126..59105329;chr15:59105126..59105300;chr15:59105126..59105274 26863196 MeRIP-seq:(Medium) rs536497004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4326404,Human_RBP_ID_6442291,Human_RBP_ID_17366903,Human_RBP_ID_22439806 RMVar_hsa_circ_80183,RMVar_hsa_circ_102093,RMVar_hsa_circ_172468,RMVar_hsa_circ_172469 102345 RMVar_ID_102345 Human_SNP_ID_579281330 m1A Human chr15 + 59105247 59105247 59105247 TCAGTCCGCGTCCCTCCCTGGGCCGGGCTGGCACTCTTGCCTTCCCCGTCCCTCATGGCGCTGCT TCAGTCCGCGTCCCTCCCTGGGCCGGGCTGGCCCTCTTGCCTTCCCCGTCCCTCATGGCGCTGCT A C CCNB2 Ensembl:ENSG00000157456 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:59105226..59105250 26863196 MeRIP-seq:(Medium) rs1206287949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232257,Human_RBP_ID_460026,Human_RBP_ID_4326412,Human_RBP_ID_5464063,Human_RBP_ID_9324286,Human_RBP_ID_22531514,Human_RBP_ID_26932362 Human_Splice_Rec_1608189,Human_Splice_Rec_1608193,Human_Splice_Rec_1608209,Human_Splice_Rec_1608219 Human_miRNA_ID_2346244,Human_miRNA_ID_2351950,Human_miRNA_ID_2398037,Human_miRNA_ID_2932495,Human_miRNA_ID_3047496 RMVar_hsa_circ_80183,RMVar_hsa_circ_102093,RMVar_hsa_circ_172468,RMVar_hsa_circ_172469 102346 RMVar_ID_102346 Human_SNP_ID_579286664 m1A Human chr15 - 59123613 59123609 59123614 GAAAACAGTAGTACTTACGATGAATTTAGTTAAGTTTTCATTTACTTTCACCACATTCTTGGCCA GAAAACAGTAGTACTTACGATGAATTTAGTT_____TTCATTTACTTTCACCACATTCTTGGCCA AAACTT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:59117275..59123670 32194978 MeRIP-seq:(Medium) rs770704262 Functional Loss DEL dbSNP153 32..36 33 - - - 102347 RMVar_ID_102347 Human_SNP_ID_579286666 m1A Human chr15 - 59123613 59123613 59123613 GAAAACAGTAGTACTTACGATGAATTTAGTTAAGTTTTCATTTACTTTCACCACATTCTTGGCCA GAAAACAGTAGTACTTACGATGAATTTAGTTACGTTTTCATTTACTTTCACCACATTCTTGGCCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:59117275..59123670 32194978 MeRIP-seq:(Medium) rs985187794 Functional Loss SNV dbSNP153 33..33 33 - - - 102348 RMVar_ID_102348 Human_SNP_ID_579293193 m1A Human chr15 - 59143847 59143847 59143847 AAATGAGATCCGAAGGCCGAGCAGGAGTTAGCAGTGCTGCCTGGGAAGTGGGCAGAGGCCAGGGG AAATGAGATCCGAAGGCCGAGCAGGAGTTAGCTGTGCTGCCTGGGAAGTGGGCAGAGGCCAGGGG T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:59143845..59143928 26863196 MeRIP-seq:(Medium) rs1209190300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172479,RMVar_hsa_circ_117730,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127918,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_172485,RMVar_hsa_circ_92316,RMVar_hsa_circ_172484,RMVar_hsa_circ_172481,RMVar_hsa_circ_172482,RMVar_hsa_circ_172480,RMVar_hsa_circ_90542,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_121151,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_172487 102349 RMVar_ID_102349 Human_SNP_ID_579398299 m1A Human chr15 + 59514422 59514422 59514422 TTGATCAGCTTTCCTTGATTGTTAAGGAAAACAGTGTAGGTATTGATGTTTAGCAAAAATTTAGT TTGATCAGCTTTCCTTGATTGTTAAGGAAAACGGTGTAGGTATTGATGTTTAGCAAAAATTTAGT A G FAM81A Ensembl:ENSG00000157470 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:59514394..59514464 26863196 MeRIP-seq:(Medium) rs759159537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1608397 RMVar_hsa_circ_43674,RMVar_hsa_circ_30592,RMVar_hsa_circ_286826 102350 RMVar_ID_102350 Human_SNP_ID_579450451 m1A Human chr15 - 59657475 59657475 59657475 GGTTTCTGCGGCGGCTGGAGAGGTGGTCGGAGAAGTAGGAACCTCCTGCCGGGCTCGTGGCGGCT GGTTTCTGCGGCGGCTGGAGAGGTGGTCGGAGGAGTAGGAACCTCCTGCCGGGCTCGTGGCGGCT T C GTF2A2,AC092755.1 Ensembl:ENSG00000140307,Ensembl:ENSG00000227161 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:59657375..59657525 26863196 MeRIP-seq:(Medium) rs547363603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758491,Human_RBP_ID_814432,Human_RBP_ID_1130403,Human_RBP_ID_4326536,Human_RBP_ID_5087864,Human_RBP_ID_5523714,Human_RBP_ID_5568796,Human_RBP_ID_6486475,Human_RBP_ID_8251494,Human_RBP_ID_8419480,Human_RBP_ID_9324287,Human_RBP_ID_12542814 Human_Splice_Rec_1608515,Human_Splice_Rec_1608523,Human_Splice_Rec_1608527,Human_Splice_Rec_1608533,Human_Splice_Rec_1608551,Human_Splice_Rec_1608557,Human_Splice_Rec_1608561,Human_Splice_Rec_1608567,Human_Splice_Rec_1608569 RMVar_hsa_circ_61686,RMVar_hsa_circ_95663,RMVar_hsa_circ_172535 102351 RMVar_ID_102351 Human_SNP_ID_579450452 m1A Human chr15 - 59657475 59657475 59657475 GGTTTCTGCGGCGGCTGGAGAGGTGGTCGGAGAAGTAGGAACCTCCTGCCGGGCTCGTGGCGGCT GGTTTCTGCGGCGGCTGGAGAGGTGGTCGGAGCAGTAGGAACCTCCTGCCGGGCTCGTGGCGGCT T G GTF2A2,AC092755.1 Ensembl:ENSG00000140307,Ensembl:ENSG00000227161 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:59657375..59657525 26863196 MeRIP-seq:(Medium) rs547363603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758491,Human_RBP_ID_814432,Human_RBP_ID_1130403,Human_RBP_ID_4326536,Human_RBP_ID_5087864,Human_RBP_ID_5523714,Human_RBP_ID_5568796,Human_RBP_ID_6486475,Human_RBP_ID_8251494,Human_RBP_ID_8419480,Human_RBP_ID_9324287,Human_RBP_ID_12542814 Human_Splice_Rec_1608515,Human_Splice_Rec_1608523,Human_Splice_Rec_1608527,Human_Splice_Rec_1608533,Human_Splice_Rec_1608551,Human_Splice_Rec_1608557,Human_Splice_Rec_1608561,Human_Splice_Rec_1608567,Human_Splice_Rec_1608569 RMVar_hsa_circ_61686,RMVar_hsa_circ_95663,RMVar_hsa_circ_172535 102352 RMVar_ID_102352 Human_SNP_ID_579482968 m1A Human chr15 + 59769052 59769052 59769052 TGAATTGGGAAAGCTCATGGAGCTTCATGGTGAAGGCAGTAGTTCTGGAAAAGCCACTGGGGACG TGAATTGGGAAAGCTCATGGAGCTTCATGGTGGAGGCAGTAGTTCTGGAAAAGCCACTGGGGACG A G RPS3AP6 Ensembl:ENSG00000234797 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1276588191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9058697,Human_RBP_ID_17367573 102353 RMVar_ID_102353 Human_SNP_ID_347501876 m1A Human chr8 - 219483 219483 219483 AATTAGGGACCAGGGTAGGGATCAGGATTTAGATTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG AATTAGGGACCAGGGTAGGGATCAGGATTTAGGTTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG T C RPL23AP53 Ensembl:ENSG00000223508 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:219480..219578 26863196 MeRIP-seq:(Medium) rs77316670 Functional Loss SNV dbSNP153 33..33 33 - - - 102354 RMVar_ID_102354 Human_SNP_ID_347501877 m1A Human chr8 - 219483 219483 219483 AATTAGGGACCAGGGTAGGGATCAGGATTTAGATTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG AATTAGGGACCAGGGTAGGGATCAGGATTTAGCTTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG T G RPL23AP53 Ensembl:ENSG00000223508 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:219480..219578 26863196 MeRIP-seq:(Medium) rs77316670 Functional Loss SNV dbSNP153 33..33 33 - - - 102355 RMVar_ID_102355 Human_SNP_ID_347572631 m1A Human chr8 + 407015 407015 407015 GCGGGCCCAGGTGGCCGGCGCGCCCGTTGGGCACTGGGGGACGCGGGCGCGTCAGGTGAAGACTG GCGGGCCCAGGTGGCCGGCGCGCCCGTTGGGCGCTGGGGGACGCGGGCGCGTCAGGTGAAGACTG A G FBXO25 Ensembl:ENSG00000147364 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:406956..413189 26863196 MeRIP-seq:(Medium) rs1282125812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995328,Human_RBP_ID_18426662,Human_RBP_ID_18452523 Human_Splice_Rec_944241,Human_Splice_Rec_944257,Human_Splice_Rec_944277 102356 RMVar_ID_102356 Human_SNP_ID_347572636 m1A Human chr8 + 407056 407027 407056 CGCGGGCGCGTCAGGTGAAGACTGGGGGCCGCAGGCGCGCTAGGTAGGTGCGGGGTGCAGCGGGC CGCG_____________________________GGCGCGCTAGGTAGGTGCGGGGTGCAGCGGGC GGGCGCGTCAGGTGAAGACTGGGGGCCGCA G FBXO25 Ensembl:ENSG00000147364 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:406976..407100 26863410 MeRIP-seq:(Medium) rs1300944780 Functional Loss DEL dbSNP153 5..33 33 - - - Human_RBP_ID_4995328,Human_RBP_ID_18426662 Human_Splice_Rec_944241,Human_Splice_Rec_944257,Human_Splice_Rec_944277 102357 RMVar_ID_102357 Human_SNP_ID_347572655 m1A Human chr8 + 407056 407056 407056 CGCGGGCGCGTCAGGTGAAGACTGGGGGCCGCAGGCGCGCTAGGTAGGTGCGGGGTGCAGCGGGC CGCGGGCGCGTCAGGTGAAGACTGGGGGCCGCGGGCGCGCTAGGTAGGTGCGGGGTGCAGCGGGC A G FBXO25 Ensembl:ENSG00000147364 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:406976..407100 26863410 MeRIP-seq:(Medium) rs1480605066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995328,Human_RBP_ID_18426662 Human_Splice_Rec_944241,Human_Splice_Rec_944257,Human_Splice_Rec_944277 102358 RMVar_ID_102358 Human_SNP_ID_347574801 m1A Human chr8 + 413005 413005 413005 ATGTTAAGAACTTTAATCTTTAAAATTAATAAATGTTCTAAGTGAAAAGAAACTTTTATGAATTA ATGTTAAGAACTTTAATCTTTAAAATTAATAAGTGTTCTAAGTGAAAAGAAACTTTTATGAATTA A G FBXO25 Ensembl:ENSG00000147364 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:413003..413098 26863410 MeRIP-seq:(Medium) rs1220970504 Functional Loss SNV dbSNP153 33..33 33 - - - 102359 RMVar_ID_102359 Human_SNP_ID_347574865 m1A Human chr8 - 413143 413143 413143 AAGTTTCTGACTACAAGATTCACATCTCTTCCAGCCATCTTCTGTCTTAATCCAACTCCATCCAG AAGTTTCTGACTACAAGATTCACATCTCTTCCTGCCATCTTCTGTCTTAATCCAACTCCATCCAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:413022..413185 26863196 MeRIP-seq:(Medium) rs1171088192 Functional Loss SNV dbSNP153 33..33 33 - - - 102360 RMVar_ID_102360 Human_SNP_ID_347604988 m1A Human chr8 - 492482 492482 492482 GCCTGGCCAGCTCTGCCAACAGCTCCAGGTGGAGCCTGCGCGCGGCAGGGAGGCTGGTGAGCATC GCCTGGCCAGCTCTGCCAACAGCTCCAGGTGGGGCCTGCGCGCGGCAGGGAGGCTGGTGAGCATC T C TDRP Ensembl:ENSG00000180190 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:492432..492549 32194978 MeRIP-seq:(Medium) rs1190959390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_944337,Human_Splice_Rec_944355 RMVar_hsa_circ_249963,RMVar_hsa_circ_333403 102361 RMVar_ID_102361 Human_SNP_ID_347609849 m1A Human chr8 + 503637 503634 503637 CTCAGCACGCACCCAACACGGAATCCAGAGCCACACACACTGGAACCAATGCCCACCTCAACACA CTCAGCACGCACCCAACACGGAATCCAGAG___CACACACTGGAACCAATGCCCACCTCAACACA GCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:503574..503712 26863196 MeRIP-seq:(Medium) rs201373016 Functional Loss DEL dbSNP153 31..33 33 - - - 102362 RMVar_ID_102362 Human_SNP_ID_347609853 m1A Human chr8 + 503637 503635 503637 CTCAGCACGCACCCAACACGGAATCCAGAGCCACACACACTGGAACCAATGCCCACCTCAACACA CTCAGCACGCACCCAACACGGAATCCAGAGC__CACACACTGGAACCAATGCCCACCTCAACACA CCA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:503574..503712 26863196 MeRIP-seq:(Medium) rs1220867148 Functional Loss DEL dbSNP153 32..33 33 - - - 102363 RMVar_ID_102363 Human_SNP_ID_347609854 m1A Human chr8 + 503637 503636 503637 CTCAGCACGCACCCAACACGGAATCCAGAGCCACACACACTGGAACCAATGCCCACCTCAACACA CTCAGCACGCACCCAACACGGAATCCAGAGCC_CACACACTGGAACCAATGCCCACCTCAACACA CA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:503574..503712 26863196 MeRIP-seq:(Medium) rs869303095 Functional Loss DEL dbSNP153 33..33 33 - - - 102364 RMVar_ID_102364 Human_SNP_ID_347671949 m1A Human chr8 - 667244 667244 667244 CAGGCACATGGGAGGAGCCCGGTGGCTGGACCAGGGGATGCACGTGACAGGGCGAGAGGCATTGA CAGGCACATGGGAGGAGCCCGGTGGCTGGACCGGGGGATGCACGTGACAGGGCGAGAGGCATTGA T C ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:666945..667245 26863196 MeRIP-seq:(Medium) rs1182491094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103571,RMVar_hsa_circ_119585,RMVar_hsa_circ_249966,RMVar_hsa_circ_249967 102365 RMVar_ID_102365 Human_SNP_ID_347672516 m1A Human chr8 - 668715 668715 668715 AGGAGCTGCTGGACCGCCTTGCGTCACACAGCATGCTGCCCTCAGACGTGTCCATCCTGTACCAC AGGAGCTGCTGGACCGCCTTGCGTCACACAGCCTGCTGCCCTCAGACGTGTCCATCCTGTACCAC T G ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:668666..668773 32194978 MeRIP-seq:(Medium) rs1477346748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958019,Human_RBP_ID_19022516,Human_RBP_ID_23117046,Human_RBP_ID_26360312 Human_Splice_Rec_944364,Human_Splice_Rec_944368,Human_Splice_Rec_944390,Human_Splice_Rec_944396 Human_miRNA_ID_1937079,Human_miRNA_ID_1948179 RMVar_hsa_circ_103571,RMVar_hsa_circ_119585,RMVar_hsa_circ_249966,RMVar_hsa_circ_249967,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_332128,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968 102366 RMVar_ID_102366 Human_SNP_ID_347672548 m1A Human chr8 - 668758 668758 668758 GTCTCCAGAGATGCAGCTTCAGCTGCCCTCGCAGATGCCGCTGAGGAGCTGCTGGACCGCCTTGC GTCTCCAGAGATGCAGCTTCAGCTGCCCTCGCGGATGCCGCTGAGGAGCTGCTGGACCGCCTTGC T C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:668707..668816 26863196 MeRIP-seq:(Medium) rs1472934907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958019,Human_RBP_ID_23117046,Human_RBP_ID_24563407,Human_RBP_ID_26360312,Human_RBP_ID_27539138 Human_Splice_Rec_944364,Human_Splice_Rec_944368,Human_Splice_Rec_944390,Human_Splice_Rec_944396 RMVar_hsa_circ_103571,RMVar_hsa_circ_119585,RMVar_hsa_circ_249966,RMVar_hsa_circ_249967,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_332128,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968 102367 RMVar_ID_102367 Human_SNP_ID_347672962 m1A Human chr8 - 669995 669995 669995 GGAAGTTGTGTCCCTGAAACAGGCCCAGGTGGAGAGGAGAGAGGACGGAGCGGGGGCAGGACGGA GGAAGTTGTGTCCCTGAAACAGGCCCAGGTGGGGAGGAGAGAGGACGGAGCGGGGGCAGGACGGA T C ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:669949..670148 26863196 MeRIP-seq:(Medium) rs1297789302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22529925 RMVar_hsa_circ_103571,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968 102368 RMVar_ID_102368 Human_SNP_ID_347673379 m1A Human chr8 - 671018 671018 671018 CGGTGGGCTCAGGTGTTGGAGCAGGGGCCGGCAGGTTCAGAGGTCGGAGCCTGGGGACCAGTGGG CGGTGGGCTCAGGTGTTGGAGCAGGGGCCGGCGGGTTCAGAGGTCGGAGCCTGGGGACCAGTGGG T C ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:670972..671048 26863196 MeRIP-seq:(Medium) rs1307679327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27843255 RMVar_hsa_circ_103571,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968 102369 RMVar_ID_102369 Human_SNP_ID_347674413 m1A Human chr8 + 673425 673425 673425 TCCTCCCCGGAGTCTGCACCCTCTTCCTCCCCAGCCCATGTCGGGTCTTCCTCGCTGGCGTCCGC TCCTCCCCGGAGTCTGCACCCTCTTCCTCCCCGGCCCATGTCGGGTCTTCCTCGCTGGCGTCCGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr8:673374..673525;chr8:673374..673540 26863196 MeRIP-seq:(Medium) rs879009358 Functional Loss SNV dbSNP153 33..33 33 - - - 102370 RMVar_ID_102370 Human_SNP_ID_347674443 m1A Human chr8 - 673481 673457 673481 AAGACCTGACACGGGCCGGGGAGGAAGACGGTAAAGACACCAGGGAGGAGGACGGTGCGGACGCC AAGACCTGACACGGGCCGGGGAGGAAGACGGT________________________GCGGACGCC CACCGTCCTCCTCCCTGGTGTCTTT C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr8:673373..673615;chr8:672203..690903 26863196 MeRIP-seq:(Medium) rs568811121 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_958753,Human_RBP_ID_8238391,Human_RBP_ID_9405158,Human_RBP_ID_9440619,Human_RBP_ID_18472461,Human_RBP_ID_22115800,Human_RBP_ID_22747384,Human_RBP_ID_24549482,Human_RBP_ID_26359601 RMVar_hsa_circ_103571,RMVar_hsa_circ_34707,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968,RMVar_hsa_circ_356503 102371 RMVar_ID_102371 Human_SNP_ID_347674458 m1A Human chr8 - 673472 673472 673472 CACGGGCCGGGGAGGAAGACGGTAAAGACACCAGGGAGGAGGACGGTGCGGACGCCAGCGAGGAA CACGGGCCGGGGAGGAAGACGGTAAAGACACCGGGGAGGAGGACGGTGCGGACGCCAGCGAGGAA T C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:673326..673842;chr8:672203..673937 26863196 MeRIP-seq:(Medium) rs573151077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958753,Human_RBP_ID_4989462,Human_RBP_ID_7847311,Human_RBP_ID_8238391,Human_RBP_ID_9405158,Human_RBP_ID_9440619,Human_RBP_ID_18472461,Human_RBP_ID_22114803,Human_RBP_ID_22747384,Human_RBP_ID_24549482,Human_RBP_ID_26193468,Human_RBP_ID_26358786 RMVar_hsa_circ_103571,RMVar_hsa_circ_34707,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968,RMVar_hsa_circ_356503 102372 RMVar_ID_102372 Human_SNP_ID_347674465 m1A Human chr8 - 673479 673478 673480 GACCTGACACGGGCCGGGGAGGAAGACGGTAAAGACACCAGGGAGGAGGACGGTGCGGACGCCAG GACCTGACACGGGCCGGGGAGGAAGACGGTA__GACACCAGGGAGGAGGACGGTGCGGACGCCAG CTT C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:673401..673618 26863196 MeRIP-seq:(Medium) rs1256857065 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_958753,Human_RBP_ID_8238391,Human_RBP_ID_9405158,Human_RBP_ID_9440619,Human_RBP_ID_18472461,Human_RBP_ID_22115800,Human_RBP_ID_22747384,Human_RBP_ID_24549482,Human_RBP_ID_26359601 RMVar_hsa_circ_103571,RMVar_hsa_circ_34707,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968,RMVar_hsa_circ_356503 102373 RMVar_ID_102373 Human_SNP_ID_347674468 m1A Human chr8 - 673481 673481 673481 AAGACCTGACACGGGCCGGGGAGGAAGACGGTAAAGACACCAGGGAGGAGGACGGTGCGGACGCC AAGACCTGACACGGGCCGGGGAGGAAGACGGTGAAGACACCAGGGAGGAGGACGGTGCGGACGCC T C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr8:673373..673615;chr8:672203..690903 26863196 MeRIP-seq:(Medium) rs149402273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958753,Human_RBP_ID_8238391,Human_RBP_ID_9405158,Human_RBP_ID_9440619,Human_RBP_ID_18472461,Human_RBP_ID_22115800,Human_RBP_ID_22747384,Human_RBP_ID_24549482,Human_RBP_ID_26359601 RMVar_hsa_circ_103571,RMVar_hsa_circ_34707,RMVar_hsa_circ_249966,RMVar_hsa_circ_57869,RMVar_hsa_circ_290215,RMVar_hsa_circ_266219,RMVar_hsa_circ_249968,RMVar_hsa_circ_356503 102374 RMVar_ID_102374 Human_SNP_ID_347674469 m1A Human chr8 + 673482 673482 673482 GCGTCCGCACCGTCCTCCTCCCTGGTGTCTTTACCGTCTTCCTCCCCGGCCCGTGTCAGGTCTTC GCGTCCGCACCGTCCTCCTCCCTGGTGTCTTTCCCGTCTTCCTCCCCGGCCCGTGTCAGGTCTTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:673301..673987 26863196 MeRIP-seq:(Medium) rs978489169 Functional Loss SNV dbSNP153 33..33 33 - - - 102375 RMVar_ID_102375 Human_SNP_ID_347677420 m1A Human chr8 + 680555 680555 680555 CCCCGGTAAACACGGAAAGTCCAAGAGAATCCACAGCTGCCACCCCTCCCCCGAAAACACGGAAA CCCCGGTAAACACGGAAAGTCCAAGAGAATCCCCAGCTGCCACCCCTCCCCCGAAAACACGGAAA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:680443..680601 26863196 MeRIP-seq:(Medium) rs1232606329 Functional Loss SNV dbSNP153 33..33 33 - - - 102376 RMVar_ID_102376 Human_SNP_ID_347683700 m1A Human chr8 + 696543 696541 696543 CCTTCCTCCCCATCAGCCTGTGCGCGCTCCTCACACCCTCCCTCTCCTTCCTCCCCATCAGCCTG CCTTCCTCCCCATCAGCCTGTGCGCGCTCCT__CACCCTCCCTCTCCTTCCTCCCCATCAGCCTG TCA T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:696462..696591 26863196 MeRIP-seq:(Medium) rs1380829857 Functional Loss DEL dbSNP153 32..33 33 - - - 102377 RMVar_ID_102377 Human_SNP_ID_347683701 m1A Human chr8 + 696543 696543 696543 CCTTCCTCCCCATCAGCCTGTGCGCGCTCCTCACACCCTCCCTCTCCTTCCTCCCCATCAGCCTG CCTTCCTCCCCATCAGCCTGTGCGCGCTCCTCCCACCCTCCCTCTCCTTCCTCCCCATCAGCCTG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:696462..696591 26863196 MeRIP-seq:(Medium) rs1473745655 Functional Loss SNV dbSNP153 33..33 33 - - - 102378 RMVar_ID_102378 Human_SNP_ID_347683702 m1A Human chr8 + 696543 696543 696543 CCTTCCTCCCCATCAGCCTGTGCGCGCTCCTCACACCCTCCCTCTCCTTCCTCCCCATCAGCCTG CCTTCCTCCCCATCAGCCTGTGCGCGCTCCTCTCACCCTCCCTCTCCTTCCTCCCCATCAGCCTG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:696462..696591 26863196 MeRIP-seq:(Medium) rs1473745655 Functional Loss SNV dbSNP153 33..33 33 - - - 102379 RMVar_ID_102379 Human_SNP_ID_347683870 m1A Human chr8 - 696924 696924 696924 GGAGGAAGGAGTGGAGGGTGAGAGAAGCGAGTACAGGCTGATGGGGAGGAAGGAGAGGGAGGGTG GGAGGAAGGAGTGGAGGGTGAGAGAAGCGAGTGCAGGCTGATGGGGAGGAAGGAGAGGGAGGGTG T C ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:696918..697066 26863196 MeRIP-seq:(Medium) rs1409591970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103571,RMVar_hsa_circ_34707,RMVar_hsa_circ_249966,RMVar_hsa_circ_266219,RMVar_hsa_circ_335493 102380 RMVar_ID_102380 Human_SNP_ID_347697228 m1A Human chr8 - 731146 731146 731146 CCGCGGCAGGGTCCCGCATGGCGGCGCACAGGAAGCACGGTAGGTGGGTGCGGTGCGGAGGCCTG CCGCGGCAGGGTCCCGCATGGCGGCGCACAGGCAGCACGGTAGGTGGGTGCGGTGCGGAGGCCTG T G ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:692533..731175 26863196 MeRIP-seq:(Medium) rs369437723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995329,Human_RBP_ID_23088037 Human_Splice_Rec_944361,Human_Splice_Rec_944383 RMVar_hsa_circ_103571,RMVar_hsa_circ_249966 102381 RMVar_ID_102381 Human_SNP_ID_347697243 m1A Human chr8 + 731160 731160 731160 GCACCCACCTACCGTGCTTCCTGTGCGCCGCCATGCGGGACCCTGCCGCGGACCTCAGACCACGG GCACCCACCTACCGTGCTTCCTGTGCGCCGCCCTGCGGGACCCTGCCGCGGACCTCAGACCACGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:715832..731213 26863196 MeRIP-seq:(Medium) rs1273359252 Functional Loss SNV dbSNP153 33..33 33 - - - 102382 RMVar_ID_102382 Human_SNP_ID_348111515 m1A Human chr8 - 1763158 1763158 1763158 CCGCGGCTGAGTCGCGCTCCGGGTGTGGACGGAGCCGGAGCCTCCCCGGGGCTCGGTGAGGACAC CCGCGGCTGAGTCGCGCTCCGGGTGTGGACGGGGCCGGAGCCTCCCCGGGGCTCGGTGAGGACAC T C AC100810.1 Ensembl:ENSG00000253982 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1763016..1764310 26863196 MeRIP-seq:(Medium) rs571635692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696582 Human_miRNA_ID_3205306 102383 RMVar_ID_102383 Human_SNP_ID_348111557 m1A Human chr8 - 1763256 1763241 1763256 CTCCGCGGGCAGCCTGGTTGCGCTGCACCCGGACGGGGCCGAGGGGACCTGAAAGCTGCGGCAGA CTCCGCGGGCAGCCTGGTTGCGCTGCACCCGG_______________CCTGAAAGCTGCGGCAGA GTCCCCTCGGCCCCGT G AC100810.1 Ensembl:ENSG00000253982 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1763210..1763294 26863196 MeRIP-seq:(Medium) rs1563100586 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_4995330,Human_RBP_ID_5630875 Human_miRNA_ID_3148076 102384 RMVar_ID_102384 Human_SNP_ID_348120122 m1A Human chr8 + 1786232 1786232 1786232 GAGGCCTGCCCTGGGGGAGGGGCTGCAGGAGGAGGGGGGGCAGGCACCCATGAGTCTGTCCAGCC GAGGCCTGCCCTGGGGGAGGGGCTGCAGGAGGGGGGGGGGCAGGCACCCATGAGTCTGTCCAGCC A G CLN8,AC019257.8 Ensembl:ENSG00000182372,Ensembl:ENSG00000283239 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:1786183..1786298 32194978 MeRIP-seq:(Medium) rs1041565813 Functional Loss SNV dbSNP153 33..33 33 - - - 102385 RMVar_ID_102385 Human_SNP_ID_348133950 m1A Human chr8 + 1824039 1824008 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC AC_______________________________GCGGGGGACGGCGGGGAACAGCGGGGGACGGC CGGCGGGGAACGGCGGGGGACGGCGGGGAACA C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs1372574069 Functional Loss DEL dbSNP153 3..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102386 RMVar_ID_102386 Human_SNP_ID_348133954 m1A Human chr8 + 1824039 1824009 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC ACG______________________________GCGGGGGACGGCGGGGAACAGCGGGGGACGGC GGCGGGGAACGGCGGGGGACGGCGGGGAACA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs1373127926 Functional Loss DEL dbSNP153 4..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102387 RMVar_ID_102387 Human_SNP_ID_348133978 m1A Human chr8 + 1824027 1824027 1824027 GGGACGCGGGGGACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACA GGGACGCGGGGGACGGCGGGGAACGGCGGGGGGCGGCGGGGAACAGCGGGGGACGGCGGGGAACA A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1823991..1824141 26863196 MeRIP-seq:(Medium) rs1047076921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102388 RMVar_ID_102388 Human_SNP_ID_348133981 m1A Human chr8 + 1824039 1824029 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC ACGGCGGGGAACGGCGGGGGACG__________GCGGGGGACGGCGGGGAACAGCGGGGGACGGC GGCGGGGAACA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs1268486648 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102389 RMVar_ID_102389 Human_SNP_ID_348133994 m1A Human chr8 + 1824039 1824038 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC ACGGCGGGGAACGGCGGGGGACGGCGGGGAAC_GCGGGGGACGGCGGGGAACAGCGGGGGACGGC CA C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs1563137477 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102390 RMVar_ID_102390 Human_SNP_ID_348133995 m1A Human chr8 + 1824039 1824039 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC ACGGCGGGGAACGGCGGGGGACGGCGGGGAACCGCGGGGGACGGCGGGGAACAGCGGGGGACGGC A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs865857680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102391 RMVar_ID_102391 Human_SNP_ID_348133996 m1A Human chr8 + 1824039 1824039 1824039 ACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACGGC ACGGCGGGGAACGGCGGGGGACGGCGGGGAACGGCGGGGGACGGCGGGGAACAGCGGGGGACGGC A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1823926..1824151 26863196 MeRIP-seq:(Medium) rs865857680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_957585,Human_RBP_ID_3887809,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5329039,Human_RBP_ID_9338142,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102392 RMVar_ID_102392 Human_SNP_ID_348134010 m1A Human chr8 + 1824082 1824062 1824082 GCGGGGAACAGCGGGGGACGGCGGGGAACAGCAGGGGACTGCGGGTCGCGTCCTGGCCGCCGAGG GCGGGGAACAGCG____________________GGGGACTGCGGGTCGCGTCCTGGCCGCCGAGG GGGGGACGGCGGGGAACAGCA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1823952..1824195 26863196 MeRIP-seq:(Medium) rs1563137520 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_268043,Human_RBP_ID_957585,Human_RBP_ID_3885221,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5243411,Human_RBP_ID_5328788,Human_RBP_ID_8944507,Human_RBP_ID_9338142,Human_RBP_ID_9440835,Human_RBP_ID_18115039,Human_RBP_ID_26358795,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102393 RMVar_ID_102393 Human_SNP_ID_348134016 m1A Human chr8 + 1824079 1824079 1824079 ACGGCGGGGAACAGCGGGGGACGGCGGGGAACAGCAGGGGACTGCGGGTCGCGTCCTGGCCGCCG ACGGCGGGGAACAGCGGGGGACGGCGGGGAACCGCAGGGGACTGCGGGTCGCGTCCTGGCCGCCG A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1823957..1824233 26863196 MeRIP-seq:(Medium) rs1323029035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_268043,Human_RBP_ID_957585,Human_RBP_ID_3885221,Human_RBP_ID_3972887,Human_RBP_ID_4999119,Human_RBP_ID_5153983,Human_RBP_ID_5243411,Human_RBP_ID_5328788,Human_RBP_ID_8944507,Human_RBP_ID_9338142,Human_RBP_ID_9440835,Human_RBP_ID_18115039,Human_RBP_ID_26358795,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102394 RMVar_ID_102394 Human_SNP_ID_348134018 m1A Human chr8 + 1824082 1824082 1824082 GCGGGGAACAGCGGGGGACGGCGGGGAACAGCAGGGGACTGCGGGTCGCGTCCTGGCCGCCGAGG GCGGGGAACAGCGGGGGACGGCGGGGAACAGCGGGGGACTGCGGGTCGCGTCCTGGCCGCCGAGG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1823952..1824195 26863196 MeRIP-seq:(Medium) rs371134437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15025,Human_RBP_ID_268043,Human_RBP_ID_957585,Human_RBP_ID_3885221,Human_RBP_ID_3972887,Human_RBP_ID_5153983,Human_RBP_ID_5243411,Human_RBP_ID_5328788,Human_RBP_ID_8944507,Human_RBP_ID_9338142,Human_RBP_ID_9440835,Human_RBP_ID_18115039,Human_RBP_ID_26358795,Human_RBP_ID_26772330 Human_Splice_Rec_944771,Human_Splice_Rec_944827,Human_Splice_Rec_944881 102395 RMVar_ID_102395 Human_SNP_ID_348134021 m1A Human chr8 - 1824089 1824089 1824089 GCACTCACCTCGGCGGCCAGGACGCGACCCGCAGTCCCCTGCTGTTCCCCGCCGTCCCCCGCTGT GCACTCACCTCGGCGGCCAGGACGCGACCCGCGGTCCCCTGCTGTTCCCCGCCGTCCCCCGCTGT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:1823989..1824165 26863196 MeRIP-seq:(Medium) rs1331468596 Functional Loss SNV dbSNP153 33..33 33 - - - 102396 RMVar_ID_102396 Human_SNP_ID_348134022 m1A Human chr8 - 1824089 1824089 1824089 GCACTCACCTCGGCGGCCAGGACGCGACCCGCAGTCCCCTGCTGTTCCCCGCCGTCCCCCGCTGT GCACTCACCTCGGCGGCCAGGACGCGACCCGCCGTCCCCTGCTGTTCCCCGCCGTCCCCCGCTGT T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:1823989..1824165 26863196 MeRIP-seq:(Medium) rs1331468596 Functional Loss SNV dbSNP153 33..33 33 - - - 102397 RMVar_ID_102397 Human_SNP_ID_348134175 m1A Human chr8 + 1824418 1824418 1824418 AGGAGCGAACTCCGATCGGCGGAAGGAGCCCGAGGGGCGAGCTGGCTTCGCCTGGGGGGTCGTGC AGGAGCGAACTCCGATCGGCGGAAGGAGCCCGCGGGGCGAGCTGGCTTCGCCTGGGGGGTCGTGC A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:1824416..1824569 32194978 MeRIP-seq:(Medium) rs1001109204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885223,Human_RBP_ID_9441075,Human_RBP_ID_17578467 102398 RMVar_ID_102398 Human_SNP_ID_348135388 m1A Human chr8 + 1827012 1827012 1827012 TGGAAAGGGGTGGGCCAGGCCCAGGGGCTGCCAAGGGTCTGAGAGGCAGGGAGAGCAGAGGCCGG TGGAAAGGGGTGGGCCAGGCCCAGGGGCTGCCGAGGGTCTGAGAGGCAGGGAGAGCAGAGGCCGG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1827008..1827107 26863196 MeRIP-seq:(Medium) rs1444682990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338569 RMVar_hsa_circ_346810 102399 RMVar_ID_102399 Human_SNP_ID_348136776 m1A Human chr8 - 1830816 1830816 1830816 CCTCGCCTGCCATGGCTCCTATTCAATTTCAAATCCCTCCTCTCCGCACCTTGTAGCCCCGTGTA CCTCGCCTGCCATGGCTCCTATTCAATTTCAAGTCCCTCCTCTCCGCACCTTGTAGCCCCGTGTA T C lnc-ERICH1-8 RNACentral:URS00008C2BE5 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1830814..1831466 26863196 MeRIP-seq:(Medium) rs1174915216 Functional Loss SNV dbSNP153 33..33 33 - - - 102400 RMVar_ID_102400 Human_SNP_ID_348137448 m1A Human chr8 + 1832394 1832367 1832395 AGACAGAGACAGAGACAGAGGCAGAGGCAGAGACAGAGAGAGGCAGAGGCAGAGACAGAGAGAGA AGACAG____________________________AGAGAGAGGCAGAGGCAGAGACAGAGAGAGA GAGACAGAGACAGAGGCAGAGGCAGAGAC G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1832390..1832521 26863196 MeRIP-seq:(Medium) rs1379279487 Functional Loss DEL dbSNP153 7..34 33 - - - Human_RBP_ID_5223423 RMVar_hsa_circ_346810 102401 RMVar_ID_102401 Human_SNP_ID_348137472 m1A Human chr8 + 1832394 1832382 1832394 AGACAGAGACAGAGACAGAGGCAGAGGCAGAGACAGAGAGAGGCAGAGGCAGAGACAGAGAGAGA AGACAGAGACAGAGACAGAGG____________CAGAGAGAGGCAGAGGCAGAGACAGAGAGAGA GCAGAGGCAGAGA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1832390..1832521 26863196 MeRIP-seq:(Medium) rs1439398950 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5223423 RMVar_hsa_circ_346810 102402 RMVar_ID_102402 Human_SNP_ID_348137480 m1A Human chr8 + 1832394 1832394 1832394 AGACAGAGACAGAGACAGAGGCAGAGGCAGAGACAGAGAGAGGCAGAGGCAGAGACAGAGAGAGA AGACAGAGACAGAGACAGAGGCAGAGGCAGAGGCAGAGAGAGGCAGAGGCAGAGACAGAGAGAGA A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1832390..1832521 26863196 MeRIP-seq:(Medium) rs1170037644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5223423 RMVar_hsa_circ_346810 102403 RMVar_ID_102403 Human_SNP_ID_348137801 m1A Human chr8 + 1832730 1832729 1832731 AGGCAGAGGCAGAGACAGAGGCAGAGAGAGACAGAGGCAGAGGCAGAGGCAGAGACAGAGACAGA AGGCAGAGGCAGAGACAGAGGCAGAGAGAGAC__AGGCAGAGGCAGAGGCAGAGACAGAGACAGA CAG C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1832726..1832816 26863196 MeRIP-seq:(Medium) rs761673482 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_346810 102404 RMVar_ID_102404 Human_SNP_ID_348138413 m1A Human chr8 + 1833340 1833324 1833341 AGACAGAAGCAGAGGGAGACAGAGACAGAGGCAGAGACAGAGGCAGAGAGAGACAGAGGCAGAGA AGACAGAAGCAGAGGGA_________________AGACAGAGGCAGAGAGAGACAGAGGCAGAGA AGACAGAGACAGAGGCAG A AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1832273..1833465 26863196 MeRIP-seq:(Medium) rs1181715638 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_14678,Human_RBP_ID_5153842,Human_RBP_ID_5404766,Human_RBP_ID_24390898 RMVar_hsa_circ_346810 102405 RMVar_ID_102405 Human_SNP_ID_348138430 m1A Human chr8 + 1833332 1833332 1833332 AGAGGCAGAGACAGAAGCAGAGGGAGACAGAGACAGAGGCAGAGACAGAGGCAGAGAGAGACAGA AGAGGCAGAGACAGAAGCAGAGGGAGACAGAGGCAGAGGCAGAGACAGAGGCAGAGAGAGACAGA A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1832271..1833421 26863196 MeRIP-seq:(Medium) rs1436900577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14678,Human_RBP_ID_5153993,Human_RBP_ID_5404766,Human_RBP_ID_24390898 RMVar_hsa_circ_346810 102406 RMVar_ID_102406 Human_SNP_ID_348138436 m1A Human chr8 + 1833340 1833338 1833340 AGACAGAAGCAGAGGGAGACAGAGACAGAGGCAGAGACAGAGGCAGAGAGAGACAGAGGCAGAGA AGACAGAAGCAGAGGGAGACAGAGACAGAGG__GAGACAGAGGCAGAGAGAGACAGAGGCAGAGA GCA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1832273..1833465 26863196 MeRIP-seq:(Medium) rs1563150269 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14678,Human_RBP_ID_5153842,Human_RBP_ID_5404766,Human_RBP_ID_24390898 RMVar_hsa_circ_346810 102407 RMVar_ID_102407 Human_SNP_ID_348140677 m1A Human chr8 + 1839071 1839039 1839071 GCTGTCTGGTGTGGAAGCTGTCCGATATGGGGACTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGA G________________________________CTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGA GCTGTCTGGTGTGGAAGCTGTCCGATATGGGGA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1839053..1839446 26863196 MeRIP-seq:(Medium) rs1437992695 Functional Loss DEL dbSNP153 2..33 33 - - - RMVar_hsa_circ_346810 102408 RMVar_ID_102408 Human_SNP_ID_348140688 m1A Human chr8 + 1839071 1839071 1839071 GCTGTCTGGTGTGGAAGCTGTCCGATATGGGGACTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGA GCTGTCTGGTGTGGAAGCTGTCCGATATGGGGGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGA A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1839053..1839446 26863196 MeRIP-seq:(Medium) rs1259001130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346810 102409 RMVar_ID_102409 Human_SNP_ID_348140908 m1A Human chr8 + 1839359 1839359 1839359 ACTGTCTGGTGTAGGGACTGTCTGGTGTGGGGACTGTCTGGTGTGGAAGCTGTCTGGTGTGGGAC ACTGTCTGGTGTAGGGACTGTCTGGTGTGGGGGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGAC A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1838781..1839663 26863196 MeRIP-seq:(Medium) rs1353296796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5658246,Human_RBP_ID_24251848 RMVar_hsa_circ_346810 102410 RMVar_ID_102410 Human_SNP_ID_348141172 m1A Human chr8 + 1839751 1839751 1839751 GGACTGTCCGGTGTGGAAGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGG GGACTGTCCGGTGTGGAAGCTGTCTGGTGTGGGAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1839744..1839930 26863196 MeRIP-seq:(Medium) rs1474699760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346810 102411 RMVar_ID_102411 Human_SNP_ID_348141173 m1A Human chr8 + 1839752 1839752 1839752 GACTGTCCGGTGTGGAAGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGGT GACTGTCCGGTGTGGAAGCTGTCTGGTGTGGAGGCTGTCTGGTGTGGGGACTGTCTGGTGTGGGT A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1839748..1839863 26863196 MeRIP-seq:(Medium) rs1373030068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346810 102412 RMVar_ID_102412 Human_SNP_ID_348141201 m1A Human chr8 + 1839785 1839785 1839785 GCTGTCTGGTGTGGGGACTGTCTGGTGTGGGTACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAG GCTGTCTGGTGTGGGGACTGTCTGGTGTGGGTGCTGTCTGGTGTGGGGACTGTCTTGTGTGGAAG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1839766..1839902 26863196 MeRIP-seq:(Medium) rs1396318428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5657993,Human_RBP_ID_27843264 RMVar_hsa_circ_346810 102413 RMVar_ID_102413 Human_SNP_ID_348141214 m1A Human chr8 + 1839816 1839800 1839816 TACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA TACTGTCTGGTGTGGGG________________GCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA GACTGTCTTGTGTGGAA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1839732..1840204 26863196 MeRIP-seq:(Medium) rs1554468994 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_5658247,Human_RBP_ID_24251863,Human_RBP_ID_27843427 RMVar_hsa_circ_346810 102414 RMVar_ID_102414 Human_SNP_ID_348141216 m1A Human chr8 + 1839816 1839801 1839817 TACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA TACTGTCTGGTGTGGGGA________________CTGTCTGGTGTGGGGACTGTCTGGTGTGGAA ACTGTCTTGTGTGGAAG A AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1839732..1840204 26863196 MeRIP-seq:(Medium) rs1404968051 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_5658247,Human_RBP_ID_24251863,Human_RBP_ID_27843427 RMVar_hsa_circ_346810 102415 RMVar_ID_102415 Human_SNP_ID_348141222 m1A Human chr8 + 1839816 1839814 1839816 TACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA TACTGTCTGGTGTGGGGACTGTCTTGTGTGG__GCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA GAA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1839732..1840204 26863196 MeRIP-seq:(Medium) rs1340633682 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5658247,Human_RBP_ID_24251863,Human_RBP_ID_27843427 RMVar_hsa_circ_346810 102416 RMVar_ID_102416 Human_SNP_ID_348141224 m1A Human chr8 + 1839816 1839816 1839816 TACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA TACTGTCTGGTGTGGGGACTGTCTTGTGTGGAGGCTGTCTGGTGTGGGGACTGTCTGGTGTGGAA A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1839732..1840204 26863196 MeRIP-seq:(Medium) rs1341436035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5658247,Human_RBP_ID_24251863,Human_RBP_ID_27843427 RMVar_hsa_circ_346810 102417 RMVar_ID_102417 Human_SNP_ID_348142948 m1A Human chr8 - 1843306 1843306 1843306 GACACTGCTTGTCACCGTTCAGGTGGATAAACATGCACTCAATAGGTGTAGGGCTGTCGACAGAG GACACTGCTTGTCACCGTTCAGGTGGATAAACGTGCACTCAATAGGTGTAGGGCTGTCGACAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1843303..1843450 26863196 MeRIP-seq:(Medium) rs1215231434 Functional Loss SNV dbSNP153 33..33 33 - - - 102418 RMVar_ID_102418 Human_SNP_ID_348143410 m1A Human chr8 + 1844412 1844404 1844412 CACCGGGGCCTGGTAGATGACAGAGACGGGAGAATCCAGGGGTCACCGGGGCCTGCTGGACGACA CACCGGGGCCTGGTAGATGACAGAG________ATCCAGGGGTCACCGGGGCCTGCTGGACGACA GACGGGAGA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:1844286..1844541 26863196 MeRIP-seq:(Medium) rs1473472763 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_14689,Human_RBP_ID_254807,Human_RBP_ID_268044,Human_RBP_ID_795525,Human_RBP_ID_3885240,Human_RBP_ID_5223432,Human_RBP_ID_5243454,Human_RBP_ID_8154714,Human_RBP_ID_8221840,Human_RBP_ID_22624397,Human_RBP_ID_24390911,Human_RBP_ID_26160209 RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_373760,RMVar_hsa_circ_374483,RMVar_hsa_circ_322345,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249992,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988 102419 RMVar_ID_102419 Human_SNP_ID_348144080 m1A Human chr8 + 1846148 1846148 1846148 CCAGGAGGGTGTCCTCGGGAGACCCTGGCGGGAGCCCGGGAGCCGCGGAGGGGCTGAGGAGCCGC CCAGGAGGGTGTCCTCGGGAGACCCTGGCGGGCGCCCGGGAGCCGCGGAGGGGCTGAGGAGCCGC A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:1846138..1846331 32194978 MeRIP-seq:(Medium) rs1264218193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_373760,RMVar_hsa_circ_374483,RMVar_hsa_circ_322345,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249992,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988 102420 RMVar_ID_102420 Human_SNP_ID_348145191 m1A Human chr8 + 1849440 1849440 1849440 GGCCGCGTGGACACAGAGGGCAAATGCTGAGGAGGGCGTGGGGCGGCCACATGGACACAGACAGC GGCCGCGTGGACACAGAGGGCAAATGCTGAGGGGGGCGTGGGGCGGCCACATGGACACAGACAGC A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1849438..1849904 26863196 MeRIP-seq:(Medium) rs1212367063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_373760,RMVar_hsa_circ_374483,RMVar_hsa_circ_322345,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249992,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988 102421 RMVar_ID_102421 Human_SNP_ID_348145297 m1A Human chr8 - 1849576 1849576 1849576 CATTTGCCGTCTGTGTCCACGCAGCTGGCCCCACGCCCTCCTCAGCATTTGCTGTCCATGCCCAC CATTTGCCGTCTGTGTCCACGCAGCTGGCCCCCCGCCCTCCTCAGCATTTGCTGTCCATGCCCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1849223..1849939 26863196 MeRIP-seq:(Medium) rs1483839524 Functional Loss SNV dbSNP153 33..33 33 - - - 102422 RMVar_ID_102422 Human_SNP_ID_348145808 m1A Human chr8 - 1850213 1850188 1850224 GCGACTGCCCCACGCCCTCCTTAGCATTTGCCATCCATGCCCATGTGGCCGCCCCACGCCCTCCT GCGACTGCCCCACGCCCTCCTCAGCATTTGCTGTCTGTGTCCACGTGGCCGCCCCACACCCTCCT CGTGGGGCGGCCACATGGGCATGGATGGCAAATGCTA TGTGGGGCGGCCACGTGGACACAGACAGCAAATGCTG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1850202..1850649 26863196 MeRIP-seq:(Medium) rs71513083 Functional Loss MNV dbSNP153 22..58 33 - - - 102423 RMVar_ID_102423 Human_SNP_ID_348145808 m1A Human chr8 + 1850200 1850188 1850224 AGGGCAAATGCTGAGGAGGGCGTGGGGCGGCCACATGGGCATGGATGGCAAATGCTAAGGAGGGC AGGGCAAATGCTGAGGAGGGTGTGGGGCGGCCACGTGGACACAGACAGCAAATGCTGAGGAGGGC CGTGGGGCGGCCACATGGGCATGGATGGCAAATGCTA TGTGGGGCGGCCACGTGGACACAGACAGCAAATGCTG AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1850175..1850672 26863196 MeRIP-seq:(Medium) rs71513083 Functional Loss MNV dbSNP153 21..57 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_373760,RMVar_hsa_circ_374483,RMVar_hsa_circ_322345,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249992,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988 102424 RMVar_ID_102424 Human_SNP_ID_348145824 m1A Human chr8 + 1850200 1850200 1850200 AGGGCAAATGCTGAGGAGGGCGTGGGGCGGCCACATGGGCATGGATGGCAAATGCTAAGGAGGGC AGGGCAAATGCTGAGGAGGGCGTGGGGCGGCCGCATGGGCATGGATGGCAAATGCTAAGGAGGGC A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1850175..1850672 26863196 MeRIP-seq:(Medium) rs112468325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_373760,RMVar_hsa_circ_374483,RMVar_hsa_circ_322345,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249992,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988 102425 RMVar_ID_102425 Human_SNP_ID_348145835 m1A Human chr8 - 1850213 1850213 1850213 GCGACTGCCCCACGCCCTCCTTAGCATTTGCCATCCATGCCCATGTGGCCGCCCCACGCCCTCCT GCGACTGCCCCACGCCCTCCTTAGCATTTGCCGTCCATGCCCATGTGGCCGCCCCACGCCCTCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1850202..1850649 26863196 MeRIP-seq:(Medium) rs116568676 Functional Loss SNV dbSNP153 33..33 33 - - - 102426 RMVar_ID_102426 Human_SNP_ID_348145836 m1A Human chr8 - 1850213 1850213 1850213 GCGACTGCCCCACGCCCTCCTTAGCATTTGCCATCCATGCCCATGTGGCCGCCCCACGCCCTCCT GCGACTGCCCCACGCCCTCCTTAGCATTTGCCCTCCATGCCCATGTGGCCGCCCCACGCCCTCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1850202..1850649 26863196 MeRIP-seq:(Medium) rs116568676 Functional Loss SNV dbSNP153 33..33 33 - - - 102427 RMVar_ID_102427 Human_SNP_ID_348155902 m1A Human chr8 + 1874713 1874713 1874713 TCTAAGACAGTCTGGAGGGAGAGTGCAGACACACACCGGGGTGTGTAAGCAGTGGAGGTTCTAAG TCTAAGACAGTCTGGAGGGAGAGTGCAGACACCCACCGGGGTGTGTAAGCAGTGGAGGTTCTAAG A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:1874679..1874814 26863196 MeRIP-seq:(Medium) rs1256801173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_343926,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249991,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_60566,RMVar_hsa_circ_249996,RMVar_hsa_circ_18234 102428 RMVar_ID_102428 Human_SNP_ID_348161122 m1A Human chr8 + 1887545 1887545 1887545 CCCTGAGTGGGGTGAGGGATACGTGAGGAAACACTGAGTTGGGTGAGGAGTCTGTGAGGAGACTG CCCTGAGTGGGGTGAGGGATACGTGAGGAAACCCTGAGTTGGGTGAGGAGTCTGTGAGGAGACTG A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:1887528..1887702;chr8:1887533..1887885 26863196 MeRIP-seq:(Medium) rs952123813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102429 RMVar_ID_102429 Human_SNP_ID_348161420 m1A Human chr8 + 1888064 1888064 1888064 AGGGTGAGGGTTGTTAGGAGACAGTGAGTGGGATGAGGGTTTATGAGGAGACACTAGGTAGGGTG AGGGTGAGGGTTGTTAGGAGACAGTGAGTGGGGTGAGGGTTTATGAGGAGACACTAGGTAGGGTG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1888052..1888220 26863196 MeRIP-seq:(Medium) rs545725068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102430 RMVar_ID_102430 Human_SNP_ID_348161807 m1A Human chr8 + 1888373 1888373 1888373 GACACTGAGTGGGGTGAGGGTTGTGAGGAGATACTGAGGTGATAGTTTTGAGGAGACAGTGGGGT GACACTGAGTGGGGTGAGGGTTGTGAGGAGATCCTGAGGTGATAGTTTTGAGGAGACAGTGGGGT A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1888334..1888558 26863196 MeRIP-seq:(Medium) rs1357528630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5224554 RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102431 RMVar_ID_102431 Human_SNP_ID_348161808 m1A Human chr8 + 1888373 1888373 1888373 GACACTGAGTGGGGTGAGGGTTGTGAGGAGATACTGAGGTGATAGTTTTGAGGAGACAGTGGGGT GACACTGAGTGGGGTGAGGGTTGTGAGGAGATGCTGAGGTGATAGTTTTGAGGAGACAGTGGGGT A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1888334..1888558 26863196 MeRIP-seq:(Medium) rs1357528630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5224554 RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102432 RMVar_ID_102432 Human_SNP_ID_348161850 m1A Human chr8 + 1888434 1888434 1888434 GGGTGAGAGTTGTGAGGAGACACTGAGTGTGGAGGGCTGTGAGGAGGCACTGAGTGGGGTGAGGG GGGTGAGAGTTGTGAGGAGACACTGAGTGTGGGGGGCTGTGAGGAGGCACTGAGTGGGGTGAGGG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1888332..1888687 26863196 MeRIP-seq:(Medium) rs559667144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102433 RMVar_ID_102433 Human_SNP_ID_348161851 m1A Human chr8 + 1888434 1888434 1888434 GGGTGAGAGTTGTGAGGAGACACTGAGTGTGGAGGGCTGTGAGGAGGCACTGAGTGGGGTGAGGG GGGTGAGAGTTGTGAGGAGACACTGAGTGTGGTGGGCTGTGAGGAGGCACTGAGTGGGGTGAGGG A T AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1888332..1888687 26863196 MeRIP-seq:(Medium) rs559667144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_249995,RMVar_hsa_circ_372071,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_347182,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249999,RMVar_hsa_circ_343644,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250002,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013 102434 RMVar_ID_102434 Human_SNP_ID_348162284 m1A Human chr8 - 1888893 1888890 1888894 CCCACTGTCTCCTCACAACCCTCACCCAACTCAGTGTCTCCTCATAACTCTCACCCCACTCAGTG CCCACTGTCTCCTCACAACCCTCACCCAACT____GTCTCCTCATAACTCTCACCCCACTCAGTG CACTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1888768..1888983 26863196 MeRIP-seq:(Medium) rs1187826453 Functional Loss DEL dbSNP153 32..35 33 - - - 102435 RMVar_ID_102435 Human_SNP_ID_348162303 m1A Human chr8 - 1888902 1888902 1888902 ACCCCTCACCCCACTGTCTCCTCACAACCCTCACCCAACTCAGTGTCTCCTCATAACTCTCACCC ACCCCTCACCCCACTGTCTCCTCACAACCCTCGCCCAACTCAGTGTCTCCTCATAACTCTCACCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:1888762..1888959;chr8:1888320..1888992 26863196 MeRIP-seq:(Medium) rs1325166110 Functional Loss SNV dbSNP153 33..33 33 - - - 102436 RMVar_ID_102436 Human_SNP_ID_348163417 m1A Human chr8 - 1890238 1890238 1890238 TCCTCACAATCCACAACCCTCAGTGCCTCCTCACAAACCCTCACCCCACTCAGTGTCTCTTCACA TCCTCACAATCCACAACCCTCAGTGCCTCCTCCCAAACCCTCACCCCACTCAGTGTCTCTTCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1890228..1890359 26863196 MeRIP-seq:(Medium) rs1394423380 Functional Loss SNV dbSNP153 33..33 33 - - - 102437 RMVar_ID_102437 Human_SNP_ID_348163545 m1A Human chr8 - 1890398 1890398 1890398 ACCCATTCAGTGTCTTCTCACAACCCTCACCCAATTCAGTGTCTCCTCACAGACTCCTCACCCAA ACCCATTCAGTGTCTTCTCACAACCCTCACCCTATTCAGTGTCTCCTCACAGACTCCTCACCCAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1889761..1890742 26863196 MeRIP-seq:(Medium) rs1268222568 Functional Loss SNV dbSNP153 33..33 33 - - - 102438 RMVar_ID_102438 Human_SNP_ID_348163546 m1A Human chr8 - 1890398 1890398 1890398 ACCCATTCAGTGTCTTCTCACAACCCTCACCCAATTCAGTGTCTCCTCACAGACTCCTCACCCAA ACCCATTCAGTGTCTTCTCACAACCCTCACCCCATTCAGTGTCTCCTCACAGACTCCTCACCCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1889761..1890742 26863196 MeRIP-seq:(Medium) rs1268222568 Functional Loss SNV dbSNP153 33..33 33 - - - 102439 RMVar_ID_102439 Human_SNP_ID_348174373 m1A Human chr8 - 1919133 1919133 1919133 CACCCACGGAACAGCTCCATCACCCATGGAACAGCTCCATCACCCATAGAACAGCTCCATCACCC CACCCACGGAACAGCTCCATCACCCATGGAACGGCTCCATCACCCATAGAACAGCTCCATCACCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1919021..1919311 26863196 MeRIP-seq:(Medium) rs1247555792 Functional Loss SNV dbSNP153 33..33 33 - - - 102440 RMVar_ID_102440 Human_SNP_ID_348174772 m1A Human chr8 + 1919837 1919818 1919837 GAGCTGTTCTGTGGGTGATGAGCTGTTCTGTCAGTGATGGAGCTGTGCTGTGGATGATGGAGCTG GAGCTGTTCTGTGG___________________GTGATGGAGCTGTGCTGTGGATGATGGAGCTG GGTGATGAGCTGTTCTGTCA G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1919726..1919856 26863196 MeRIP-seq:(Medium) rs1418424140 Functional Loss DEL dbSNP153 15..33 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_29318,RMVar_hsa_circ_347372,RMVar_hsa_circ_250008,RMVar_hsa_circ_112063,RMVar_hsa_circ_250006,RMVar_hsa_circ_81593,RMVar_hsa_circ_250009,RMVar_hsa_circ_250011,RMVar_hsa_circ_317763,RMVar_hsa_circ_377056,RMVar_hsa_circ_250010 102441 RMVar_ID_102441 Human_SNP_ID_348174789 m1A Human chr8 + 1919837 1919837 1919837 GAGCTGTTCTGTGGGTGATGAGCTGTTCTGTCAGTGATGGAGCTGTGCTGTGGATGATGGAGCTG GAGCTGTTCTGTGGGTGATGAGCTGTTCTGTCGGTGATGGAGCTGTGCTGTGGATGATGGAGCTG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1919726..1919856 26863196 MeRIP-seq:(Medium) rs1337268390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98986,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_29318,RMVar_hsa_circ_347372,RMVar_hsa_circ_250008,RMVar_hsa_circ_112063,RMVar_hsa_circ_250006,RMVar_hsa_circ_81593,RMVar_hsa_circ_250009,RMVar_hsa_circ_250011,RMVar_hsa_circ_317763,RMVar_hsa_circ_377056,RMVar_hsa_circ_250010 102442 RMVar_ID_102442 Human_SNP_ID_348205529 m1A Human chr8 - 2001469 2001469 2001469 GGGCTCTTCCGGGCACGCGCGCTCCTCAGGGGACGCGAGCTCCTCCGGGGACGCGGCGCCCGCGC GGGCTCTTCCGGGCACGCGCGCTCCTCAGGGGGCGCGAGCTCCTCCGGGGACGCGGCGCCCGCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:2001419..2001569 32194978 MeRIP-seq:(Medium) rs1309487403 Functional Loss SNV dbSNP153 33..33 33 - - - 102443 RMVar_ID_102443 Human_SNP_ID_348206632 m1A Human chr8 - 2003248 2003248 2003248 CCTGGGTCTCAAGGCATCCACCCCCAGAAGCAAAGACAAGCAAAAGGAAAGCAAAGCGAAAGCGG CCTGGGTCTCAAGGCATCCACCCCCAGAAGCACAGACAAGCAAAAGGAAAGCAAAGCGAAAGCGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:2002413..2003358 32194978 MeRIP-seq:(Medium) rs1007339012 Functional Loss SNV dbSNP153 33..33 33 - - - 102444 RMVar_ID_102444 Human_SNP_ID_350300886 m1A Human chr8 - 6405768 6405768 6405768 TCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCCTGCCCCGGAAGCAACCAG TCCACCCTGCCGGCAACCAGGCTCAAACCTGCGGCCCGCGGATCCCCTGCCCCGGAAGCAACCAG T C AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:6405724..6405824 32194978 MeRIP-seq:(Medium) rs58969519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102445 RMVar_ID_102445 Human_SNP_ID_350300887 m1A Human chr8 - 6405768 6405768 6405768 TCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCCTGCCCCGGAAGCAACCAG TCCACCCTGCCGGCAACCAGGCTCAAACCTGCCGCCCGCGGATCCCCTGCCCCGGAAGCAACCAG T G AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:6405724..6405824 32194978 MeRIP-seq:(Medium) rs58969519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102446 RMVar_ID_102446 Human_SNP_ID_350300898 m1A Human chr8 - 6405786 6405784 6405786 GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCC GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGC_ACCAGGCTCAAACCTGCAGCCCGCGGATCCCC GTT GT AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879900595 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102447 RMVar_ID_102447 Human_SNP_ID_350300899 m1A Human chr8 - 6405785 6405785 6405786 CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCCT CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCTCCCAGGCTCAAACCTGCAGCCCGCGGATCCCCT TT GA AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34796322 Functional Loss MNV dbSNP153 32..33 33 - - - Human_Splice_Rec_946651 102448 RMVar_ID_102448 Human_SNP_ID_350300899 m1A Human chr8 - 6405786 6405785 6405786 GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCC GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCTCCCAGGCTCAAACCTGCAGCCCGCGGATCCCC TT GA AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34796322 Functional Loss MNV dbSNP153 33..34 33 - - - Human_Splice_Rec_946651 102449 RMVar_ID_102449 Human_SNP_ID_350300900 m1A Human chr8 - 6405785 6405785 6405785 CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCCT CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCATCCAGGCTCAAACCTGCAGCCCGCGGATCCCCT T A AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2243660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102450 RMVar_ID_102450 Human_SNP_ID_350300901 m1A Human chr8 - 6405785 6405785 6405785 CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCCT CTTGGCCCTCCAGCTGCTCCACCCTGCCGGCACCCAGGCTCAAACCTGCAGCCCGCGGATCCCCT T G AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2243660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102451 RMVar_ID_102451 Human_SNP_ID_350300902 m1A Human chr8 - 6405786 6405786 6405786 GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCC GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCTACCAGGCTCAAACCTGCAGCCCGCGGATCCCC T A AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2243661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102452 RMVar_ID_102452 Human_SNP_ID_350300903 m1A Human chr8 - 6405786 6405786 6405786 GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCAACCAGGCTCAAACCTGCAGCCCGCGGATCCCC GCTTGGCCCTCCAGCTGCTCCACCCTGCCGGCGACCAGGCTCAAACCTGCAGCCCGCGGATCCCC T C AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2243661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_946651 102453 RMVar_ID_102453 Human_SNP_ID_350301288 m1A Human chr8 + 6406453 6406453 6406453 TACTCCCAGGAGAAGAGAAAAACCCACGGCCCAGCAGCCAGAGGCGCGGCGAGGCGGAATCGGGC TACTCCCAGGAGAAGAGAAAAACCCACGGCCCTGCAGCCAGAGGCGCGGCGAGGCGGAATCGGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:6406403..6406523 26863196 MeRIP-seq:(Medium) rs954239926 Functional Loss SNV dbSNP153 33..33 33 - - - 102454 RMVar_ID_102454 Human_SNP_ID_350303133 m1A Human chr8 + 6409836 6409836 6409836 GTCACAGGTGTGGACATCGTCCCATGTCAGGCATGGTTAGGATGAAGAGTGGTGACAGAGGAGCG GTCACAGGTGTGGACATCGTCCCATGTCAGGCGTGGTTAGGATGAAGAGTGGTGACAGAGGAGCG A G MCPH1 Ensembl:ENSG00000147316 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:6409830..6409929 26863196 MeRIP-seq:(Medium) rs971345833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16451180 102455 RMVar_ID_102455 Human_SNP_ID_350357743 m1A Human chr8 - 6549574 6549574 6549574 CAACTCAAGATGCAGAAGGCTTCCCGCCCTGCACGCGGCTCCCTCACGCCCCTCCTCATCCATAT CAACTCAAGATGCAGAAGGCTTCCCGCCCTGCTCGCGGCTCCCTCACGCCCCTCCTCATCCATAT T A ANGPT2 Ensembl:ENSG00000091879 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:6549527..6549656 26863196 MeRIP-seq:(Medium) rs1311369449 Functional Loss SNV dbSNP153 33..33 33 - - - 102456 RMVar_ID_102456 Human_SNP_ID_350872430 m1A Human chr8 - 8228053 8228053 8228053 GCCGGGGCAGGGCGTTGACTATGTCGTACCACATGGCCAGGCGGTGCGCGGACTCTGGGAGGCGG GCCGGGGCAGGGCGTTGACTATGTCGTACCACTTGGCCAGGCGGTGCGCGGACTCTGGGAGGCGG T A FAM85B RNACentral:URS00008C2977 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8228006..8228103 26863196 MeRIP-seq:(Medium) rs1264938708 Functional Loss SNV dbSNP153 33..33 33 - - - 102457 RMVar_ID_102457 Human_SNP_ID_350872781 m1A Human chr8 + 8228747 8228747 8228747 GAGCGGAGAGGCCCGCGGGGCTCGCGGAGTCCAGGGGCAGACGGGATGGGTCTCCGTGCTGAAAC GAGCGGAGAGGCCCGCGGGGCTCGCGGAGTCCCGGGGCAGACGGGATGGGTCTCCGTGCTGAAAC A C FAM86B3P Ensembl:ENSG00000173295 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:8228642..8228754;chr8:8228647..8228770 26863196 MeRIP-seq:(Medium) rs1385347240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_947477 102458 RMVar_ID_102458 Human_SNP_ID_350874799 m1A Human chr8 - 8234177 8234177 8234177 GGTAGGGAAACGTGGATGGGAGGGCCTTCAGCAAGAGGTGTTCAGAGGGTAGGGTTAGGTGTAGT GGTAGGGAAACGTGGATGGGAGGGCCTTCAGCTAGAGGTGTTCAGAGGGTAGGGTTAGGTGTAGT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8234126..8234211 26863196 MeRIP-seq:(Medium) rs1434641337 Functional Loss SNV dbSNP153 33..33 33 - - - 102459 RMVar_ID_102459 Human_SNP_ID_350874802 m1A Human chr8 + 8234182 8234182 8234182 ACCTAACCCTACCCTCTGAACACCTCTTGCTGAAGGCCCTCCCATCCACGTTTCCCTACCAAGTG ACCTAACCCTACCCTCTGAACACCTCTTGCTGGAGGCCCTCCCATCCACGTTTCCCTACCAAGTG A G FAM86B3P Ensembl:ENSG00000173295 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:8234132..8234252 26863196 MeRIP-seq:(Medium) rs1475167274 Functional Loss SNV dbSNP153 33..33 33 - - - 102460 RMVar_ID_102460 Human_SNP_ID_350878817 m1A Human chr8 + 8244504 8244504 8244504 CTTGATATTCCTGGAGGGTCACGGGAAGCGCTATGTGAATCCCACTTCTGATATTGTAAGATTCT CTTGATATTCCTGGAGGGTCACGGGAAGCGCTTTGTGAATCCCACTTCTGATATTGTAAGATTCT A T FAM86B3P Ensembl:ENSG00000173295 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:8244412..8244503 26863196 MeRIP-seq:(Medium) rs1326497601 Functional Loss SNV dbSNP153 33..33 33 - - - 102461 RMVar_ID_102461 Human_SNP_ID_350878818 m1A Human chr8 - 8244505 8244505 8244505 GAGAATCTTACAATATCAGAAGTGGGATTCACATAGCGCTTCCCGTGACCCTCCAGGAATATCAA GAGAATCTTACAATATCAGAAGTGGGATTCACGTAGCGCTTCCCGTGACCCTCCAGGAATATCAA T C ALG1L13P Ensembl:ENSG00000253981 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8244409..8244504 26863196 MeRIP-seq:(Medium) rs950759212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995334 Human_Splice_Rec_947511,Human_Splice_Rec_947523 102462 RMVar_ID_102462 Human_SNP_ID_350912574 m1A Human chr8 + 8337843 8337843 8337843 ACCTCCGGCAGCTCTCTGTCTCCCACCTGCACAGATTGCTGTGAGAGCCGTGTACAATTCAGCCC ACCTCCGGCAGCTCTCTGTCTCCCACCTGCACGGATTGCTGTGAGAGCCGTGTACAATTCAGCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:8337792..8338179 26863196 MeRIP-seq:(Medium) rs1306517609 Functional Loss SNV dbSNP153 33..33 33 - - - 102463 RMVar_ID_102463 Human_SNP_ID_351111201 m1A Human chr8 - 8891999 8891999 8891999 GCCTGGAGGAGCTCGTGCTGCAGGGGAACCAGATCGCGGTGCTGCCCGACCACTTTGGCCAGCTC GCCTGGAGGAGCTCGTGCTGCAGGGGAACCAGGTCGCGGTGCTGCCCGACCACTTTGGCCAGCTC T C MFHAS1 Ensembl:ENSG00000147324 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:8891948..8892099 32194978 MeRIP-seq:(Medium) rs756427852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8691443,Human_RBP_ID_27540568 102464 RMVar_ID_102464 Human_SNP_ID_351111786 m1A Human chr8 - 8892922 8892922 8892922 CGCCGCCGGGGCCTGCCCCGGGGCCGGGGCCGACGCGCTCGAGTCCCCCGCCTCCCCCCAGCTCG CGCCGCCGGGGCCTGCCCCGGGGCCGGGGCCGGCGCGCTCGAGTCCCCCGCCTCCCCCCAGCTCG T C MFHAS1 Ensembl:ENSG00000147324 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:8892882..8892959 26863196 MeRIP-seq:(Medium) rs555281714 Functional Loss SNV dbSNP153 33..33 33 - - - 102465 RMVar_ID_102465 Human_SNP_ID_351111788 m1A Human chr8 + 8892941 8892923 8892941 GGACTCGAGCGCGTCGGCCCCGGCCCCGGGGCAGGCCCCGGCGGCGGTAAGCGTGAGCTGGCGCA GGACTCGAGCGCGTC__________________GGCCCCGGCGGCGGTAAGCGTGAGCTGGCGCA CGGCCCCGGCCCCGGGGCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8892893..8892998 26863196 MeRIP-seq:(Medium) rs758770393 Functional Loss DEL dbSNP153 16..33 33 - - - 102466 RMVar_ID_102466 Human_SNP_ID_351111798 m1A Human chr8 + 8892941 8892929 8892941 GGACTCGAGCGCGTCGGCCCCGGCCCCGGGGCAGGCCCCGGCGGCGGTAAGCGTGAGCTGGCGCA GGACTCGAGCGCGTCGGCCCC____________GGCCCCGGCGGCGGTAAGCGTGAGCTGGCGCA CGGCCCCGGGGCA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8892893..8892998 26863196 MeRIP-seq:(Medium) rs566247640 Functional Loss DEL dbSNP153,HGVD 22..33 33 - - - 102467 RMVar_ID_102467 Human_SNP_ID_351111939 m1A Human chr8 - 8893111 8893111 8893111 CAGGAGCCGGAGGGCCCGGGGCGCGGCGCGGCATGTAGCTGCGGGCTCCCGCGTCCGCGTGAGGC CAGGAGCCGGAGGGCCCGGGGCGCGGCGCGGCGTGTAGCTGCGGGCTCCCGCGTCCGCGTGAGGC T C MFHAS1 Ensembl:ENSG00000147324 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:8893075..8893213 26863196 MeRIP-seq:(Medium) rs1306176045 Functional Loss SNV dbSNP153 33..33 33 - - - 102468 RMVar_ID_102468 Human_SNP_ID_351112068 m1A Human chr8 + 8893419 8893419 8893419 GGGGGGCCCGGCTCCGGCCCCGCTACCCTCGCAGCCGCGGTCCCGCGGCCGGCAGCGGCGTCGCC GGGGGGCCCGGCTCCGGCCCCGCTACCCTCGCGGCCGCGGTCCCGCGGCCGGCAGCGGCGTCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:8893385..8893575 26863196 MeRIP-seq:(Medium) rs1327663831 Functional Loss SNV dbSNP153 33..33 33 - - - 102469 RMVar_ID_102469 Human_SNP_ID_351162568 m1A Human chr8 + 9032336 9032336 9032336 AATTTATTATTAGCTGTGTTAACTTTTATTCTATGCTTCATATGCTCTGACATTGACATAGTGGA AATTTATTATTAGCTGTGTTAACTTTTATTCTGTGCTTCATATGCTCTGACATTGACATAGTGGA A G ERI1 Ensembl:ENSG00000104626 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11780338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17640110,Human_RBP_ID_18393092,Human_RBP_ID_26557556 GWAS_ID_13419,GWAS_ID_13420,GWAS_ID_13421 102470 RMVar_ID_102470 Human_SNP_ID_351162569 m1A Human chr8 + 9032336 9032336 9032336 AATTTATTATTAGCTGTGTTAACTTTTATTCTATGCTTCATATGCTCTGACATTGACATAGTGGA AATTTATTATTAGCTGTGTTAACTTTTATTCTTTGCTTCATATGCTCTGACATTGACATAGTGGA A T ERI1 Ensembl:ENSG00000104626 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11780338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17640110,Human_RBP_ID_18393092,Human_RBP_ID_26557556 GWAS_ID_13419,GWAS_ID_13420,GWAS_ID_13421 102471 RMVar_ID_102471 Human_SNP_ID_351348382 m1A Human chr8 - 9555777 9555777 9555777 GGAGGGAAGTATTGGGAGCTCAGAGAACAGCCAAGGGAACGGGGCGGGGCTTTGTCACTGAGAGG GGAGGGAAGTATTGGGAGCTCAGAGAACAGCCCAGGGAACGGGGCGGGGCTTTGTCACTGAGAGG T G AC021242.3 Ensembl:ENSG00000272267 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:9555733..9555832 26863196 MeRIP-seq:(Medium) rs1005007881 Functional Loss SNV dbSNP153 33..33 33 - - - 102472 RMVar_ID_102472 Human_SNP_ID_351348663 m1A Human chr8 - 9556191 9556188 9556191 GTGCTGGTGGTACTGCAACAGCTGGTACCGTCAACCGGGTCCGGGGATCGGGGCCTGTCGGGCGG GTGCTGGTGGTACTGCAACAGCTGGTACCGTC___CGGGTCCGGGGATCGGGGCCTGTCGGGCGG GGTT G AC021242.3 Ensembl:ENSG00000272267 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:9556144..9556373 26863196 MeRIP-seq:(Medium) rs1322949427 Functional Loss DEL dbSNP153 33..35 33 - - - 102473 RMVar_ID_102473 Human_SNP_ID_351348757 m1A Human chr8 - 9556330 9556330 9556330 GGAAGATGAGGAAGAAGTCGGGGAAGAAGAGGACGACGGTGAATTGTTACTGCCACTGCCGGCTG GGAAGATGAGGAAGAAGTCGGGGAAGAAGAGGGCGACGGTGAATTGTTACTGCCACTGCCGGCTG T C AC021242.3 Ensembl:ENSG00000272267 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:9556226..9556395 26863196 MeRIP-seq:(Medium) rs1306613329 Functional Loss SNV dbSNP153 33..33 33 - - - 102474 RMVar_ID_102474 Human_SNP_ID_351348804 m1A Human chr8 - 9556415 9556406 9556415 CTGCCCCAGGCCCCAGTGGTGCTGTGCTGCTAACTCCGGCCGCCTCGGGGCTCTCCGCCAAGCTC CTGCCCCAGGCCCCAGTGGTGCTGTGCTGCTA_________GCCTCGGGGCTCTCCGCCAAGCTC CGGCCGGAGT C AC021242.3 Ensembl:ENSG00000272267 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:9556273..9556471 26863196 MeRIP-seq:(Medium) rs1192003700 Functional Loss DEL dbSNP153 33..41 33 - - - 102475 RMVar_ID_102475 Human_SNP_ID_351420769 m1A Human chr8 + 9771137 9771136 9771137 TATGAGAGAAAGAGAAACCAAGGAAGGGAGGGAAGGAGAGAGAGAGAGACAGACAGGAAGGAAAG TATGAGAGAAAGAGAAACCAAGGAAGGGAGGG_AGGAGAGAGAGAGAGACAGACAGGAAGGAAAG GA G TNKS Ensembl:ENSG00000173273 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:9771127..9771263 26863196 MeRIP-seq:(Medium) rs1471740918 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_95985,RMVar_hsa_circ_250127,RMVar_hsa_circ_268530 102476 RMVar_ID_102476 Human_SNP_ID_351421128 m1A Human chr8 + 9771560 9771560 9771560 AGGGAGAAAGACTGAGAGAGGAAGCAAGGGAGAAAGCGAGAGAGGAAGGAAGAGAGAAAGGGAGA AGGGAGAAAGACTGAGAGAGGAAGCAAGGGAGGAAGCGAGAGAGGAAGGAAGAGAGAAAGGGAGA A G TNKS Ensembl:ENSG00000173273 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:9771027..9771902 26863196 MeRIP-seq:(Medium) rs1204791314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070433,Human_RBP_ID_26194224 RMVar_hsa_circ_95985,RMVar_hsa_circ_250127,RMVar_hsa_circ_268530 102477 RMVar_ID_102477 Human_SNP_ID_351421129 m1A Human chr8 + 9771561 9771561 9771561 GGGAGAAAGACTGAGAGAGGAAGCAAGGGAGAAAGCGAGAGAGGAAGGAAGAGAGAAAGGGAGAG GGGAGAAAGACTGAGAGAGGAAGCAAGGGAGAGAGCGAGAGAGGAAGGAAGAGAGAAAGGGAGAG A G TNKS Ensembl:ENSG00000173273 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:9771081..9771897 26863196 MeRIP-seq:(Medium) rs1348198010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17070433,Human_RBP_ID_26194224 RMVar_hsa_circ_95985,RMVar_hsa_circ_250127,RMVar_hsa_circ_268530 102478 RMVar_ID_102478 Human_SNP_ID_351421505 m1A Human chr8 - 9772051 9772024 9772051 CTCTCTCCCTCTCTCCCCCTCCATCCCTCCCTACCTCTGTCTCCTCTCACTCCCTCCCTTTCTCC CTCTCTCCCTCTCTCCCCCTCCATCCCTCCCT___________________________TTCTCC AAGGGAGGGAGTGAGAGGAGACAGAGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:9772012..9772155 26863196 MeRIP-seq:(Medium) rs1478316907 Functional Loss DEL dbSNP153 33..59 33 - - - 102479 RMVar_ID_102479 Human_SNP_ID_351421520 m1A Human chr8 - 9772051 9772051 9772051 CTCTCTCCCTCTCTCCCCCTCCATCCCTCCCTACCTCTGTCTCCTCTCACTCCCTCCCTTTCTCC CTCTCTCCCTCTCTCCCCCTCCATCCCTCCCTCCCTCTGTCTCCTCTCACTCCCTCCCTTTCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:9772012..9772155 26863196 MeRIP-seq:(Medium) rs1247999949 Functional Loss SNV dbSNP153 33..33 33 - - - 102480 RMVar_ID_102480 Human_SNP_ID_351421549 m1A Human chr8 - 9772115 9772085 9772115 TACATGATGAGTCCCATGTCATCCCTCCCTCCACCCGTCCTTCCCTGTTTCTCCCTCCCTCCTTC TACATGATGAGTCCCATGTCATCCCTCCCTCC______________________________TTC AGGAGGGAGGGAGAAACAGGGAAGGACGGGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:9772065..9772233 26863196 MeRIP-seq:(Medium) rs1396047166 Functional Loss DEL dbSNP153 33..62 33 - - - 102481 RMVar_ID_102481 Human_SNP_ID_351421563 m1A Human chr8 - 9772115 9772115 9772115 TACATGATGAGTCCCATGTCATCCCTCCCTCCACCCGTCCTTCCCTGTTTCTCCCTCCCTCCTTC TACATGATGAGTCCCATGTCATCCCTCCCTCCGCCCGTCCTTCCCTGTTTCTCCCTCCCTCCTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:9772065..9772233 26863196 MeRIP-seq:(Medium) rs764071632 Functional Loss SNV dbSNP153 33..33 33 - - - 102482 RMVar_ID_102482 Human_SNP_ID_351423651 m1A Human chr8 - 9777590 9777590 9777590 CCTTCACAGCCTCCCCAGTTTTTTCACCTTGGAACTCAAGCCCGTGTCAACCTGCATCTCCAGTA CCTTCACAGCCTCCCCAGTTTTTTCACCTTGGGACTCAAGCCCGTGTCAACCTGCATCTCCAGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:9777539..9777628 26863196 MeRIP-seq:(Medium) rs1255755483 Functional Loss SNV dbSNP153 33..33 33 - - - 102483 RMVar_ID_102483 Human_SNP_ID_351523505 m1A Human chr8 - 10054410 10054410 10054410 AGTGGGGTCCGCGGCCGGAACCGGGGGGCGGCAGGGGCGCGGGCGGGCGGGCGCGGGGCGCTGCT AGTGGGGTCCGCGGCCGGAACCGGGGGGCGGCGGGGGCGCGGGCGGGCGGGCGCGGGGCGCTGCT T C AC034111.2 Ensembl:ENSG00000286622 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:10054364..10054554 26863196 MeRIP-seq:(Medium) rs1361513262 Functional Loss SNV dbSNP153 33..33 33 - - - 102484 RMVar_ID_102484 Human_SNP_ID_351523506 m1A Human chr8 - 10054410 10054410 10054410 AGTGGGGTCCGCGGCCGGAACCGGGGGGCGGCAGGGGCGCGGGCGGGCGGGCGCGGGGCGCTGCT AGTGGGGTCCGCGGCCGGAACCGGGGGGCGGCCGGGGCGCGGGCGGGCGGGCGCGGGGCGCTGCT T G AC034111.2 Ensembl:ENSG00000286622 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:10054364..10054554 26863196 MeRIP-seq:(Medium) rs1361513262 Functional Loss SNV dbSNP153 33..33 33 - - - 102485 RMVar_ID_102485 Human_SNP_ID_351523618 m1A Human chr8 + 10054580 10054580 10054580 TCCTCCTCCTCCACAGCCTCTTTCCCGTCCCGAGGATGGGCAACTCGGCCTCGAACATCGTCAGC TCCTCCTCCTCCACAGCCTCTTTCCCGTCCCGTGGATGGGCAACTCGGCCTCGAACATCGTCAGC A T MSRA Ensembl:ENSG00000175806 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:10054440..10054580 26863196 MeRIP-seq:(Medium) rs757211389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_948395,Human_Splice_Rec_948405,Human_Splice_Rec_948413 102486 RMVar_ID_102486 Human_SNP_ID_351813580 m1A Human chr8 - 10805532 10805532 10805532 GTGGCCCCTTCCTGTGCTCTGCCTCCTCCCTCAGCACTAGTGTGGCCCCTTCCTGTGCTCTGTCA GTGGCCCCTTCCTGTGCTCTGCCTCCTCCCTCGGCACTAGTGTGGCCCCTTCCTGTGCTCTGTCA T C PINX1,PINX1:2 Ensembl:ENSG00000254093,Ensembl:ENSG00000258724 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:10805517..10805644 26863196 MeRIP-seq:(Medium) rs1203283290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21571079 102487 RMVar_ID_102487 Human_SNP_ID_351820908 m1A Human chr8 + 10825526 10825526 10825526 TCCAATGCAAGATCGCCACCTAGTGGCTGAAGACAACAACCGCATGCACAAATGATTTCACATAC TCCAATGCAAGATCGCCACCTAGTGGCTGAAGGCAACAACCGCATGCACAAATGATTTCACATAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:10825504..10825617 26863196 MeRIP-seq:(Medium) rs955875209 Functional Loss SNV dbSNP153 33..33 33 - - - 102488 RMVar_ID_102488 Human_SNP_ID_351826293 m1A Human chr8 + 10839827 10839827 10839827 TGACTGCGGCCACTGGGCGGGCTGGAGACTCCAGGAGAATCAGGACGTGCGTAACTCCCTCGCCG TGACTGCGGCCACTGGGCGGGCTGGAGACTCCCGGAGAATCAGGACGTGCGTAACTCCCTCGCCG A C LOC101929229 RNACentral:URS00009AF328 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:10834689..10839847 26863196 MeRIP-seq:(Medium) rs915712554 Functional Loss SNV dbSNP153 33..33 33 - - - 102489 RMVar_ID_102489 Human_SNP_ID_351948329 m1A Human chr8 + 11200945 11200945 11200945 CGTCCCCGAAGAACACCAGCAGCGCCAGCACGATCCACAGGCAGTCGAGCCACGGCCGCTCCACC CGTCCCCGAAGAACACCAGCAGCGCCAGCACGGTCCACAGGCAGTCGAGCCACGGCCGCTCCACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11200902..11201017 32194978 MeRIP-seq:(Medium) rs1314352640 Functional Loss SNV dbSNP153 33..33 33 - - - 102490 RMVar_ID_102490 Human_SNP_ID_351992492 m1A Human chr8 + 11326195 11326195 11326195 TTGAAAGATCTGCTTCAAGGCATAACTCGTGTAGTTGTCTGGTTTCAGGGATAGCTGTTTGAATT TTGAAAGATCTGCTTCAAGGCATAACTCGTGTCGTTGTCTGGTTTCAGGGATAGCTGTTTGAATT A C MTMR9 Ensembl:ENSG00000104643 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2572401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250216,RMVar_hsa_circ_105716,RMVar_hsa_circ_250226 102491 RMVar_ID_102491 Human_SNP_ID_352149994 m1A Human chr8 + 11769777 11769777 11769777 TGCGTAGCGGTGCTGGGTCGGGCCGACGTGCCACCCACCCGGAGCCGGTGAGTGCAGCCGCCCGC TGCGTAGCGGTGCTGGGTCGGGCCGACGTGCCCCCCACCCGGAGCCGGTGAGTGCAGCCGCCCGC A C NEIL2 Ensembl:ENSG00000154328 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:11769729..11769927 26863196 MeRIP-seq:(Medium) rs964876986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995338 Human_Splice_Rec_949129,Human_Splice_Rec_949137,Human_Splice_Rec_949147,Human_Splice_Rec_949153,Human_Splice_Rec_949159 RMVar_hsa_circ_77367,RMVar_hsa_circ_250232 102492 RMVar_ID_102492 Human_SNP_ID_352150005 m1A Human chr8 - 11769793 11769793 11769793 GCAGATCTACCGGAGGGCGGGCGGCTGCACTCACCGGCTCCGGGTGGGTGGCACGTCGGCCCGAC GCAGATCTACCGGAGGGCGGGCGGCTGCACTCGCCGGCTCCGGGTGGGTGGCACGTCGGCCCGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:11769742..11769923;chr8:11769747..11769881;chr8:11769771..11769942 26863196 MeRIP-seq:(Medium) rs1033626045 Functional Loss SNV dbSNP153 33..33 33 - - - 102493 RMVar_ID_102493 Human_SNP_ID_352164754 m1A Human chr8 - 11802853 11802853 11802853 CGCACCAGGTTGTAGAACTCTTCGGGGTGGCCAAGGCATTTCACGAACTCCATCCTGGCGCAGGC CGCACCAGGTTGTAGAACTCTTCGGGGTGGCCGAGGCATTTCACGAACTCCATCCTGGCGCAGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:11802751..11802925 26863410 MeRIP-seq:(Medium) rs1047643 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_13422,GWAS_ID_13423 102494 RMVar_ID_102494 Human_SNP_ID_352168116 m1A Human chr8 + 11808738 11808709 11808739 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAG______________________________TCCCACTCCTGCTCCTCGACGTCTCCCACCG GTCCCACTCCCACTCCCACTCCCACTCCCAC G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs71711801 Functional Loss DEL dbSNP153 5..34 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102495 RMVar_ID_102495 Human_SNP_ID_352168117 m1A Human chr8 + 11808738 11808709 11808739 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCAC________________________TCCCACTCCTGCTCCTCGACGTCTCCCACCG GTCCCACTCCCACTCCCACTCCCACTCCCAC GTCCCAC FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs71711801 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102496 RMVar_ID_102496 Human_SNP_ID_352168118 m1A Human chr8 + 11808738 11808709 11808739 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCAC__________________TCCCACTCCTGCTCCTCGACGTCTCCCACCG GTCCCACTCCCACTCCCACTCCCACTCCCAC GTCCCACTCCCAC FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs71711801 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102497 RMVar_ID_102497 Human_SNP_ID_352168119 m1A Human chr8 + 11808738 11808709 11808739 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCAC____________TCCCACTCCTGCTCCTCGACGTCTCCCACCG GTCCCACTCCCACTCCCACTCCCACTCCCAC GTCCCACTCCCACTCCCAC FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs71711801 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102498 RMVar_ID_102498 Human_SNP_ID_352168120 m1A Human chr8 + 11808738 11808709 11808739 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCACTCCCAC______TCCCACTCCTGCTCCTCGACGTCTCCCACCG GTCCCACTCCCACTCCCACTCCCACTCCCAC GTCCCACTCCCACTCCCACTCCCAC FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs71711801 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102499 RMVar_ID_102499 Human_SNP_ID_352168131 m1A Human chr8 + 11808720 11808717 11808720 GCTGTGGAGCCGCCTGCCCCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCT GCTGTGGAGCCGCCTGCCCCAGTCCCACTC___CTCCCACTCCCACTCCCACTCCCACTCCTGCT CCCA C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:11808718..11808850 26863196 MeRIP-seq:(Medium) rs1275886257 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102500 RMVar_ID_102500 Human_SNP_ID_352168133 m1A Human chr8 + 11808720 11808720 11808720 GCTGTGGAGCCGCCTGCCCCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCT GCTGTGGAGCCGCCTGCCCCAGTCCCACTCCCCCTCCCACTCCCACTCCCACTCCCACTCCTGCT A C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:11808718..11808850 26863196 MeRIP-seq:(Medium) rs939737618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102501 RMVar_ID_102501 Human_SNP_ID_352168134 m1A Human chr8 + 11808720 11808720 11808720 GCTGTGGAGCCGCCTGCCCCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCT GCTGTGGAGCCGCCTGCCCCAGTCCCACTCCCGCTCCCACTCCCACTCCCACTCCCACTCCTGCT A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:11808718..11808850 26863196 MeRIP-seq:(Medium) rs939737618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102502 RMVar_ID_102502 Human_SNP_ID_352168152 m1A Human chr8 + 11808738 11808733 11808738 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCACTCCCAC_____CTCCCACTCCTGCTCCTCGACGTCTCCCACCG CTCCCA C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs1221265979 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102503 RMVar_ID_102503 Human_SNP_ID_352168157 m1A Human chr8 + 11808738 11808735 11808738 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCACTCCCACTC___CTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCCA C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs546829075 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102504 RMVar_ID_102504 Human_SNP_ID_352168165 m1A Human chr8 + 11808738 11808738 11808738 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCACTCCCACTCCCCCTCCCACTCCTGCTCCTCGACGTCTCCCACCG A C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs79689996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102505 RMVar_ID_102505 Human_SNP_ID_352168166 m1A Human chr8 + 11808738 11808738 11808738 CCAGTCCCACTCCCACTCCCACTCCCACTCCCACTCCCACTCCTGCTCCTCGACGTCTCCCACCG CCAGTCCCACTCCCACTCCCACTCCCACTCCCGCTCCCACTCCTGCTCCTCGACGTCTCCCACCG A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11808735..11808825 26863196 MeRIP-seq:(Medium) rs79689996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094066,Human_RBP_ID_19140736,Human_RBP_ID_22626018,Human_RBP_ID_27843271 RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_250236 102506 RMVar_ID_102506 Human_SNP_ID_352175096 m1A Human chr8 - 11821851 11821851 11821851 CTAACCTTGTCCCACTCCTGTTCAGAGGTCACATGCTTATCCAAAAACTCTGCCATCCCAATGCC CTAACCTTGTCCCACTCCTGTTCAGAGGTCACGTGCTTATCCAAAAACTCTGCCATCCCAATGCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:11821801..11821900 32194978 MeRIP-seq:(Medium) rs1400137203 Functional Loss SNV dbSNP153 33..33 33 - - - 102507 RMVar_ID_102507 Human_SNP_ID_352180354 m1A Human chr8 + 11831629 11831629 11831629 AAGCAGTGACCCTGATGATGGATGCCACCAATATGCCAGCTGTCAAAGCCATCATATATCAGTAT AAGCAGTGACCCTGATGATGGATGCCACCAATGTGCCAGCTGTCAAAGCCATCATATATCAGTAT A G FDFT1 Ensembl:ENSG00000079459 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11831579..11831713 26863196 MeRIP-seq:(Medium) rs1467716511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693325,Human_RBP_ID_1692595,Human_RBP_ID_2051842,Human_RBP_ID_17319135,Human_RBP_ID_18124813,Human_RBP_ID_22464842,Human_RBP_ID_24241902 Human_Splice_Rec_949189,Human_Splice_Rec_949207,Human_Splice_Rec_949223,Human_Splice_Rec_949247,Human_Splice_Rec_949255,Human_Splice_Rec_949267,Human_Splice_Rec_949293,Human_Splice_Rec_949307,Human_Splice_Rec_949331,Human_Splice_Rec_949351,Human_Splice_Rec_949365,Human_Splice_Rec_949381,Human_Splice_Rec_949393,Human_Splice_Rec_949421,Human_Splice_Rec_949431 Human_miRNA_ID_259627,Human_miRNA_ID_263420,Human_miRNA_ID_2042915,Human_miRNA_ID_2045065 RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_266866,RMVar_hsa_circ_52043,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_250242 102508 RMVar_ID_102508 Human_SNP_ID_352183859 m1A Human chr8 + 11838461 11838461 11838461 AACAAGGCAGATCATCTCCACCATCCGGACGCAGAATCTTCCCAACTGTCAGCTGATTTCCCGAA AACAAGGCAGATCATCTCCACCATCCGGACGCGGAATCTTCCCAACTGTCAGCTGATTTCCCGAA A G FDFT1 Ensembl:ENSG00000079459 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:11838387..11838571;chr8:11838381..11838578 26863196 MeRIP-seq:(Medium) rs189378553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693326,Human_RBP_ID_796649,Human_RBP_ID_1692601,Human_RBP_ID_2051843,Human_RBP_ID_7803012,Human_RBP_ID_16324118,Human_RBP_ID_17316949,Human_RBP_ID_17431726,Human_RBP_ID_24241924,Human_RBP_ID_27535449 Human_Splice_Rec_949190,Human_Splice_Rec_949208,Human_Splice_Rec_949224,Human_Splice_Rec_949248,Human_Splice_Rec_949256,Human_Splice_Rec_949268,Human_Splice_Rec_949294,Human_Splice_Rec_949308,Human_Splice_Rec_949332,Human_Splice_Rec_949352,Human_Splice_Rec_949366,Human_Splice_Rec_949382,Human_Splice_Rec_949394,Human_Splice_Rec_949422,Human_Splice_Rec_949432 RMVar_hsa_circ_266866,RMVar_hsa_circ_250237 102509 RMVar_ID_102509 Human_SNP_ID_352184101 m1A Human chr8 - 11838888 11838888 11838888 ACTAAGTAGGATCTCATGACAGTCACATATGCAGCGACTTCACCTAAACCGTGGCACTGAATGCT ACTAAGTAGGATCTCATGACAGTCACATATGCGGCGACTTCACCTAAACCGTGGCACTGAATGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:11838805..11838891 32194978 MeRIP-seq:(Medium) rs1241443979 Functional Loss SNV dbSNP153 33..33 33 - - - 102510 RMVar_ID_102510 Human_SNP_ID_352187732 m1A Human chr8 + 11844884 11844884 11844884 AGTCAGCTGGGGCAGCAGGTACTCCCTACGGCACTAGTCTACAGGGGGAAGGACGCTCTGTGCTG AGTCAGCTGGGGCAGCAGGTACTCCCTACGGCGCTAGTCTACAGGGGGAAGGACGCTCTGTGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11844751..11844925 32194978 MeRIP-seq:(Medium) rs957123874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3132007 102511 RMVar_ID_102511 Human_SNP_ID_352188371 m1A Human chr8 - 11845717 11845717 11845717 TGCCATCCGCATCCTGGGCTGGGGAGTGGAGAATGGCACACCCTACTGGCTGGTTGCCAACTCCT TGCCATCCGCATCCTGGGCTGGGGAGTGGAGATTGGCACACCCTACTGGCTGGTTGCCAACTCCT T A CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11845640..11845735 26863196 MeRIP-seq:(Medium) rs1212824063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693400,Human_RBP_ID_795855,Human_RBP_ID_845226,Human_RBP_ID_958376,Human_RBP_ID_5153850,Human_RBP_ID_9338602,Human_RBP_ID_17319938,Human_RBP_ID_18111793,Human_RBP_ID_22464847,Human_RBP_ID_22775599 Human_Splice_Rec_949445,Human_Splice_Rec_949466,Human_Splice_Rec_949467,Human_Splice_Rec_949474,Human_Splice_Rec_949475,Human_Splice_Rec_949492,Human_Splice_Rec_949493,Human_Splice_Rec_949514,Human_Splice_Rec_949515,Human_Splice_Rec_949536,Human_Splice_Rec_949537,Human_Splice_Rec_949554,Human_Splice_Rec_949555,Human_Splice_Rec_949574,Human_Splice_Rec_949575,Human_Splice_Rec_949594,Human_Splice_Rec_949595,Human_Splice_Rec_949614,Human_Splice_Rec_949615,Human_Splice_Rec_949622 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_70495,RMVar_hsa_circ_90587,RMVar_hsa_circ_250246,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247 102512 RMVar_ID_102512 Human_SNP_ID_352188401 m1A Human chr8 - 11845750 11845750 11845750 CCAACACGTCACCGGAGAGATGATGGGTGGCCATGCCATCCGCATCCTGGGCTGGGGAGTGGAGA CCAACACGTCACCGGAGAGATGATGGGTGGCCGTGCCATCCGCATCCTGGGCTGGGGAGTGGAGA T C CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11845701..11845750 32194978 MeRIP-seq:(Medium) rs1373655221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958376,Human_RBP_ID_9338602,Human_RBP_ID_17319938,Human_RBP_ID_22464847,Human_RBP_ID_22775599 Human_Splice_Rec_949445,Human_Splice_Rec_949466,Human_Splice_Rec_949467,Human_Splice_Rec_949474,Human_Splice_Rec_949475,Human_Splice_Rec_949492,Human_Splice_Rec_949493,Human_Splice_Rec_949514,Human_Splice_Rec_949515,Human_Splice_Rec_949536,Human_Splice_Rec_949537,Human_Splice_Rec_949554,Human_Splice_Rec_949555,Human_Splice_Rec_949574,Human_Splice_Rec_949575,Human_Splice_Rec_949594,Human_Splice_Rec_949595,Human_Splice_Rec_949614,Human_Splice_Rec_949615,Human_Splice_Rec_949622 Human_miRNA_ID_1348949,Human_miRNA_ID_2492948,Human_miRNA_ID_2674804,Human_miRNA_ID_2925557 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_70495,RMVar_hsa_circ_90587,RMVar_hsa_circ_250246,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247 102513 RMVar_ID_102513 Human_SNP_ID_352189510 m1A Human chr8 - 11847167 11847167 11847167 TCCCCAACCCCGAGCTCGGTTCATTTTCCAGGATACAATTCCTACAGCGTCTCCAATAGCGAGAA TCCCCAACCCCGAGCTCGGTTCATTTTCCAGGCTACAATTCCTACAGCGTCTCCAATAGCGAGAA T G CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11847132..11847203 26863196 MeRIP-seq:(Medium) rs755196993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795856,Human_RBP_ID_17319940,Human_RBP_ID_17433778,Human_RBP_ID_22775602 Human_Splice_Rec_949464,Human_Splice_Rec_949472,Human_Splice_Rec_949490,Human_Splice_Rec_949512,Human_Splice_Rec_949534,Human_Splice_Rec_949552,Human_Splice_Rec_949572,Human_Splice_Rec_949592,Human_Splice_Rec_949612,Human_Splice_Rec_949620,Human_Splice_Rec_949628,Human_Splice_Rec_949634 Human_miRNA_ID_2238528 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_70495,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247,RMVar_hsa_circ_109660,RMVar_hsa_circ_250248 102514 RMVar_ID_102514 Human_SNP_ID_352190007 m1A Human chr8 - 11847824 11847822 11847824 TAGGTTGACTCCGCTTTCTCCCGCGTCCCATCAGGGTGCAGACCGTACTCCATCCCTCCCTGTGA TAGGTTGACTCCGCTTTCTCCCGCGTCCCATC__GGTGCAGACCGTACTCCATCCCTCCCTGTGA CCT C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11847776..11847825 32194978 MeRIP-seq:(Medium) rs1407009377 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4968766,Human_RBP_ID_18472466,Human_RBP_ID_22465081,Human_RBP_ID_22624453,Human_RBP_ID_22688053,Human_RBP_ID_22775810,Human_RBP_ID_22836111 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_8724,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247 102515 RMVar_ID_102515 Human_SNP_ID_352190168 m1A Human chr8 + 11848028 11848028 11848028 AAATAAAGCCATGATGGTTAATTGCTCAAACAATCCATCTGGCCAGAAAGTGGCCAAGGGGACAC AAATAAAGCCATGATGGTTAATTGCTCAAACAGTCCATCTGGCCAGAAAGTGGCCAAGGGGACAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11848025..11848102 26863196 MeRIP-seq:(Medium) rs1473523530 Functional Loss SNV dbSNP153 33..33 33 - - - 102516 RMVar_ID_102516 Human_SNP_ID_352190939 m1A Human chr8 - 11849131 11849131 11849131 CCTTCGGGGCTGTGGAAGCCATCTCTGACCGGATCTGCATCCACACCAATGCGCACGTCAGCGTG CCTTCGGGGCTGTGGAAGCCATCTCTGACCGGGTCTGCATCCACACCAATGCGCACGTCAGCGTG T C CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11849026..11849175 32194978 MeRIP-seq:(Medium) rs760309398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179543,Human_RBP_ID_693405,Human_RBP_ID_795860,Human_RBP_ID_1692614,Human_RBP_ID_3972914,Human_RBP_ID_4994896,Human_RBP_ID_18472469,Human_RBP_ID_22465086,Human_RBP_ID_22775608,Human_RBP_ID_27362047 Human_Splice_Rec_949458,Human_Splice_Rec_949459,Human_Splice_Rec_949484,Human_Splice_Rec_949485,Human_Splice_Rec_949506,Human_Splice_Rec_949507,Human_Splice_Rec_949528,Human_Splice_Rec_949529,Human_Splice_Rec_949566,Human_Splice_Rec_949567,Human_Splice_Rec_949586,Human_Splice_Rec_949587,Human_Splice_Rec_949606,Human_Splice_Rec_949607,Human_Splice_Rec_949623,Human_Splice_Rec_949636,Human_Splice_Rec_949637,Human_Splice_Rec_949648,Human_Splice_Rec_949649,Human_Splice_Rec_949658,Human_Splice_Rec_949659,Human_Splice_Rec_949668,Human_Splice_Rec_949669,Human_Splice_Rec_949678,Human_Splice_Rec_949679,Human_Splice_Rec_949688,Human_Splice_Rec_949696,Human_Splice_Rec_949704,Human_Splice_Rec_949714 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247,RMVar_hsa_circ_2156,RMVar_hsa_circ_21333 102517 RMVar_ID_102517 Human_SNP_ID_352193272 m1A Human chr8 - 11853408 11853408 11853408 GGCCTCCCTCTGCTGCCTGCTGGTGTTGGCCAATGCCCGGAGCAGGCCCTCTTTCCATCCCCTGT GGCCTCCCTCTGCTGCCTGCTGGTGTTGGCCAGTGCCCGGAGCAGGCCCTCTTTCCATCCCCTGT T C CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11852665..11853500 32194978 MeRIP-seq:(Medium) rs751312364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88841,Human_RBP_ID_693409,Human_RBP_ID_795865,Human_RBP_ID_845229,Human_RBP_ID_4994898,Human_RBP_ID_5329044,Human_RBP_ID_8944511,Human_RBP_ID_18196479,Human_RBP_ID_22465091 Human_Splice_Rec_949452,Human_Splice_Rec_949453,Human_Splice_Rec_949478,Human_Splice_Rec_949479,Human_Splice_Rec_949500,Human_Splice_Rec_949501,Human_Splice_Rec_949522,Human_Splice_Rec_949523,Human_Splice_Rec_949542,Human_Splice_Rec_949543,Human_Splice_Rec_949560,Human_Splice_Rec_949561,Human_Splice_Rec_949580,Human_Splice_Rec_949581,Human_Splice_Rec_949600,Human_Splice_Rec_949601,Human_Splice_Rec_949642,Human_Splice_Rec_949643,Human_Splice_Rec_949652,Human_Splice_Rec_949653,Human_Splice_Rec_949662,Human_Splice_Rec_949663,Human_Splice_Rec_949672,Human_Splice_Rec_949673,Human_Splice_Rec_949682,Human_Splice_Rec_949683,Human_Splice_Rec_949690,Human_Splice_Rec_949691,Human_Splice_Rec_949698,Human_Splice_Rec_949699,Human_Splice_Rec_949708,Human_Splice_Rec_949709,Human_Splice_Rec_949715,Human_Splice_Rec_949719,Human_Splice_Rec_949728,Human_Splice_Rec_949729,Human_Splice_Rec_949738,Human_Splice_Rec_949739,Human_Splice_Rec_949746,Human_Splice_Rec_949747,Human_Splice_Rec_949756,Human_Splice_Rec_949757,Human_Splice_Rec_949760,Human_Splice_Rec_949761,Human_Splice_Rec_949768,Human_Splice_Rec_949769,Human_Splice_Rec_949774,Human_Splice_Rec_949775,Human_Splice_Rec_949778 RMVar_hsa_circ_5419,RMVar_hsa_circ_55110,RMVar_hsa_circ_38356,RMVar_hsa_circ_19822,RMVar_hsa_circ_2156,RMVar_hsa_circ_21333,RMVar_hsa_circ_333238,RMVar_hsa_circ_341226,RMVar_hsa_circ_342718,RMVar_hsa_circ_314115,RMVar_hsa_circ_54959,RMVar_hsa_circ_250250,RMVar_hsa_circ_250251,RMVar_hsa_circ_303321,RMVar_hsa_circ_250249,RMVar_hsa_circ_356959,RMVar_hsa_circ_289568,RMVar_hsa_circ_250253,RMVar_hsa_circ_9698,RMVar_hsa_circ_250254,RMVar_hsa_circ_250252,RMVar_hsa_circ_82533,RMVar_hsa_circ_250257 102518 RMVar_ID_102518 Human_SNP_ID_352193286 m1A Human chr8 + 11853423 11853423 11853423 AGGGCCTGCTCCGGGCATTGGCCAACACCAGCAGGCAGCAGAGGGAGGCCCAGAGCTGCCACATG AGGGCCTGCTCCGGGCATTGGCCAACACCAGCGGGCAGCAGAGGGAGGCCCAGAGCTGCCACATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:11852665..11853449 32194978 MeRIP-seq:(Medium) rs1486395922 Functional Loss SNV dbSNP153 33..33 33 - - - 102519 RMVar_ID_102519 Human_SNP_ID_352193325 m1A Human chr8 + 11853472 11853472 11853472 CCAGAGCTGCCACATGTTGGAAGCCGGATCCTAGATCCACCTGGAGAGGACAGAGGGCATCAGGA CCAGAGCTGCCACATGTTGGAAGCCGGATCCTTGATCCACCTGGAGAGGACAGAGGGCATCAGGA A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:11853426..11853542 26863410 MeRIP-seq:(Medium) rs1030989463 Functional Loss SNV dbSNP153 33..33 33 - - - 102520 RMVar_ID_102520 Human_SNP_ID_352199991 m1A Human chr8 - 11868058 11868058 11868058 GGCGGCTGCAGGGCTCCGGCAACCGCTCCGGCAACGCCAACCGCTCCGCTGCGCGCAGGCTGGGC GGCGGCTGCAGGGCTCCGGCAACCGCTCCGGCGACGCCAACCGCTCCGCTGCGCGCAGGCTGGGC T C CTSB Ensembl:ENSG00000164733 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:11867953..11868060 26863196 MeRIP-seq:(Medium) rs1468937547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795870,Human_RBP_ID_845001,Human_RBP_ID_4994902,Human_RBP_ID_5328795,Human_RBP_ID_9338177,Human_RBP_ID_18172424,Human_RBP_ID_22465092,Human_RBP_ID_22534407 Human_Splice_Rec_949451,Human_Splice_Rec_949477,Human_Splice_Rec_949497,Human_Splice_Rec_949519,Human_Splice_Rec_949539,Human_Splice_Rec_949557,Human_Splice_Rec_949577,Human_Splice_Rec_949597,Human_Splice_Rec_949641,Human_Splice_Rec_949671,Human_Splice_Rec_949723,Human_Splice_Rec_949733,Human_Splice_Rec_949743,Human_Splice_Rec_949751,Human_Splice_Rec_949763,Human_Splice_Rec_949779 RMVar_hsa_circ_5419,RMVar_hsa_circ_342718,RMVar_hsa_circ_82533,RMVar_hsa_circ_250257 102521 RMVar_ID_102521 Human_SNP_ID_352200001 m1A Human chr8 + 11868064 11868064 11868064 CCTGCGCGCAGCGGAGCGGTTGGCGTTGCCGGAGCGGTTGCCGGAGCCCTGCAGCCGCCGTAGCC CCTGCGCGCAGCGGAGCGGTTGGCGTTGCCGGCGCGGTTGCCGGAGCCCTGCAGCCGCCGTAGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:11867929..11868075 26863196 MeRIP-seq:(Medium) rs1021548742 Functional Loss SNV dbSNP153 33..33 33 - - - 102522 RMVar_ID_102522 Human_SNP_ID_352417966 m1A Human chr8 + 12565677 12565676 12565678 GAGAGAGAGAGAGACCGTAAAAGAAGGGAGACAAAGAGATAAAAGGTGCGAGTGAGCAGGTGAGG GAGAGAGAGAGAGACCGTAAAAGAAGGGAGAC__AGAGATAAAAGGTGCGAGTGAGCAGGTGAGG CAA C LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5 RNACentral:URS00009BC63E,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12565626..12565709 26863196 MeRIP-seq:(Medium) rs1197344609 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 102523 RMVar_ID_102523 Human_SNP_ID_352459370 m1A Human chr8 - 12649301 12649298 12649301 GTTGCAGTGAGGAGGAGGTTGCGGTGAGGAGGAGGTTGCGGTGAGGAGGAGGTTGCAGTGAGGAG GTTGCAGTGAGGAGGAGGTTGCGGTGAGGAGG___TTGCGGTGAGGAGGAGGTTGCAGTGAGGAG ACCT A AC068587.4 Ensembl:ENSG00000283674 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:12649252..12649329 26863196 MeRIP-seq:(Medium) rs1050503778 Functional Loss DEL dbSNP153 33..35 33 - - - 102524 RMVar_ID_102524 Human_SNP_ID_352465076 m1A Human chr8 - 12659170 12659170 12659170 CGAGGACGGGGAGGACGCGCTGCGGCCGGGCAAGGAGGACACCGGCACCCAGACAGGTGGCGACG CGAGGACGGGGAGGACGCGCTGCGGCCGGGCAGGGAGGACACCGGCACCCAGACAGGTGGCGACG T C AC068587.7,AC068587.4 Ensembl:ENSG00000284724,Ensembl:ENSG00000283674 Pseudogene,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:12659124..12659292;chr8:12659119..12659268 26863196 MeRIP-seq:(Medium) rs2898343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_950195,Human_Splice_Rec_950211,Human_Splice_Rec_950227 102525 RMVar_ID_102525 Human_SNP_ID_352465613 m1A Human chr8 - 12659574 12659574 12659574 AGGGACAGCGACCTCCTGGGCCAGGACAGGTGAGCGCGGCGCAGGCCCGGGCCCGGCGTGTCCGC AGGGACAGCGACCTCCTGGGCCAGGACAGGTGCGCGCGGCGCAGGCCCGGGCCCGGCGTGTCCGC T G AC068587.4 Ensembl:ENSG00000283674 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12659466..12659586 26863196 MeRIP-seq:(Medium) rs1338025136 Functional Loss SNV dbSNP153 33..33 33 - - - 102526 RMVar_ID_102526 Human_SNP_ID_352469323 m1A Human chr8 + 12665414 12665414 12665414 GCAACAGCCGCAGCCTCTTCTCTTCGGGAGGGACGTCGTCCTCCTCCCTCCTGGGCCAGCCATCC GCAACAGCCGCAGCCTCTTCTCTTCGGGAGGGGCGTCGTCCTCCTCCCTCCTGGGCCAGCCATCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12665374..12665562 26863196 MeRIP-seq:(Medium) rs1248001467 Functional Loss SNV dbSNP153 33..33 33 - - - 102527 RMVar_ID_102527 Human_SNP_ID_352469324 m1A Human chr8 + 12665414 12665414 12665414 GCAACAGCCGCAGCCTCTTCTCTTCGGGAGGGACGTCGTCCTCCTCCCTCCTGGGCCAGCCATCC GCAACAGCCGCAGCCTCTTCTCTTCGGGAGGGTCGTCGTCCTCCTCCCTCCTGGGCCAGCCATCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12665374..12665562 26863196 MeRIP-seq:(Medium) rs1248001467 Functional Loss SNV dbSNP153 33..33 33 - - - 102528 RMVar_ID_102528 Human_SNP_ID_352469412 m1A Human chr8 + 12665540 12665540 12665540 CTCTGCCTGCACTTGGGGAAGAAGAAGGACCCAGCGCGAGCGTCCTCTCGGCGGAGCTGGGGAGT CTCTGCCTGCACTTGGGGAAGAAGAAGGACCCGGCGCGAGCGTCCTCTCGGCGGAGCTGGGGAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:12659391..12665596 26863196 MeRIP-seq:(Medium) rs1264784597 Functional Loss SNV dbSNP153 33..33 33 - - - 102529 RMVar_ID_102529 Human_SNP_ID_352509528 m1A Human chr8 - 12754185 12754185 12754185 GTCTCCCTTCCTCACCCACAAAAGTCACCGGGACAATTGGGAACCGCGGGAGGGCAGAATTGCAT GTCTCCCTTCCTCACCCACAAAAGTCACCGGGTCAATTGGGAACCGCGGGAGGGCAGAATTGCAT T A LONRF1 Ensembl:ENSG00000154359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:12754183..12754334 26863196 MeRIP-seq:(Medium) rs1456190242 Functional Loss SNV dbSNP153 33..33 33 - - - 102530 RMVar_ID_102530 Human_SNP_ID_352510078 m1A Human chr8 - 12755305 12755305 12755305 GGAAGTGGGCGGCGGCAGCGGCCATCGGCTGGAGCGCGCGGCCGCGGAGTCGGAGCGCTGGGAGC GGAAGTGGGCGGCGGCAGCGGCCATCGGCTGGGGCGCGCGGCCGCGGAGTCGGAGCGCTGGGAGC T C LONRF1 Ensembl:ENSG00000154359 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12755255..12755454 26863196 MeRIP-seq:(Medium) rs1004380421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796373,Human_RBP_ID_4994906,Human_RBP_ID_18466990 102531 RMVar_ID_102531 Human_SNP_ID_352510094 m1A Human chr8 + 12755339 12755339 12755339 CAGCCGATGGCCGCTGCCGCCGCCCACTTCCCAGAACCGGCCTCGGCCCTGCGGCGCTGGGGCCA CAGCCGATGGCCGCTGCCGCCGCCCACTTCCCGGAACCGGCCTCGGCCCTGCGGCGCTGGGGCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:12755290..12755451 26863196 MeRIP-seq:(Medium) rs1420762326 Functional Loss SNV dbSNP153 33..33 33 - - - 102532 RMVar_ID_102532 Human_SNP_ID_352510095 m1A Human chr8 + 12755339 12755339 12755339 CAGCCGATGGCCGCTGCCGCCGCCCACTTCCCAGAACCGGCCTCGGCCCTGCGGCGCTGGGGCCA CAGCCGATGGCCGCTGCCGCCGCCCACTTCCCTGAACCGGCCTCGGCCCTGCGGCGCTGGGGCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:12755290..12755451 26863196 MeRIP-seq:(Medium) rs1420762326 Functional Loss SNV dbSNP153 33..33 33 - - - 102533 RMVar_ID_102533 Human_SNP_ID_352580724 m1A Human chr8 - 12951665 12951665 12951665 CCTTCACCTTTCGGGAGGCGGCGCTCGGGCTCAGCTGTCCGGGAACCCAGGCCTGCGGCGCCTCC CCTTCACCTTTCGGGAGGCGGCGCTCGGGCTCCGCTGTCCGGGAACCCAGGCCTGCGGCGCCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:12951626..12951697 26863196 MeRIP-seq:(Medium) rs963379211 Functional Loss SNV dbSNP153 33..33 33 - - - 102534 RMVar_ID_102534 Human_SNP_ID_352580811 m1A Human chr8 + 12951857 12951855 12951858 GGCGGGCCAAGCTGGCCTGCGGCCGCGGCGGGAAGAAGGGCTAGCGAAGCACCCCCGACCGGGCC GGCGGGCCAAGCTGGCCTGCGGCCGCGGCGG___GAAGGGCTAGCGAAGCACCCCCGACCGGGCC GGAA G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:12951808..12951953 26863196 MeRIP-seq:(Medium) rs1011531708 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_694615 102535 RMVar_ID_102535 Human_SNP_ID_352580814 m1A Human chr8 + 12951857 12951857 12951857 GGCGGGCCAAGCTGGCCTGCGGCCGCGGCGGGAAGAAGGGCTAGCGAAGCACCCCCGACCGGGCC GGCGGGCCAAGCTGGCCTGCGGCCGCGGCGGGGAGAAGGGCTAGCGAAGCACCCCCGACCGGGCC A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:12951808..12951953 26863196 MeRIP-seq:(Medium) rs1022127277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_694615 102536 RMVar_ID_102536 Human_SNP_ID_352580849 m1A Human chr8 - 12951919 12951919 12951919 GGCTCGTGTCGGGGCTTCCAAAGAGAAGTTGCAGCGAGGCGCCCCCCGGCGTCCGGCGCCTGGGC GGCTCGTGTCGGGGCTTCCAAAGAGAAGTTGCCGCGAGGCGCCCCCCGGCGTCCGGCGCCTGGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:12951824..12952040 26863196 MeRIP-seq:(Medium) rs899274643 Functional Loss SNV dbSNP153 33..33 33 - - - 102537 RMVar_ID_102537 Human_SNP_ID_352635473 m1A Human chr8 - 13084360 13084360 13084360 AGAGCTGTAAGAAGGATTTTTATTTTGTTATAATTTAGTTACCATTTTCAGTGTTATTTCAAAGG AGAGCTGTAAGAAGGATTTTTATTTTGTTATAGTTTAGTTACCATTTTCAGTGTTATTTCAAAGG T C DLC1 Ensembl:ENSG00000164741 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:13084309..13084510 32194978 MeRIP-seq:(Medium) rs1180482774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7812668,Human_RBP_ID_24246012,Human_RBP_ID_27774148 Human_miRNA_ID_2059726,Human_miRNA_ID_2185123,Human_miRNA_ID_2246914,Human_miRNA_ID_2851221 RMVar_hsa_circ_75979,RMVar_hsa_circ_82077,RMVar_hsa_circ_124966,RMVar_hsa_circ_250281,RMVar_hsa_circ_250282,RMVar_hsa_circ_250280 102538 RMVar_ID_102538 Human_SNP_ID_352693319 m1A Human chr8 - 13249941 13249941 13249941 CCCCAAGCCATCCTGGAGGGTTCTGGCAGGCAAAAACAATTCAGGAAGAGTGGATGACAGGTGGA CCCCAAGCCATCCTGGAGGGTTCTGGCAGGCACAAACAATTCAGGAAGAGTGGATGACAGGTGGA T G DLC1 Ensembl:ENSG00000164741 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:13249930..13250042 32194978 MeRIP-seq:(Medium) rs942480771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97181,RMVar_hsa_circ_250288,RMVar_hsa_circ_122887,RMVar_hsa_circ_250291 102539 RMVar_ID_102539 Human_SNP_ID_288326285 m1A Human chr6 + 96521629 96521629 96521629 AGCCCTGCATCCTGCCCACGACCCCCCCAGAAACACCTACGCACCACTCTCCTAGCCGCCGCAGC AGCCCTGCATCCTGCCCACGACCCCCCCAGAACCACCTACGCACCACTCTCCTAGCCGCCGCAGC A C UFL1 Ensembl:ENSG00000014123 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:96521583..96521662 26863196 MeRIP-seq:(Medium) rs922537391 Functional Loss SNV dbSNP153 33..33 33 - - - 102540 RMVar_ID_102540 Human_SNP_ID_288326517 m1A Human chr6 + 96521943 96521943 96521943 CCGACTTCCAGCGGGCGCAGTTCGCCGAGGCCACGCAGAGGTGCCCGACCCTCCCTCTCCTTTGT CCGACTTCCAGCGGGCGCAGTTCGCCGAGGCCTCGCAGAGGTGCCCGACCCTCCCTCTCCTTTGT A T UFL1 Ensembl:ENSG00000014123 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:96521895..96521999;chr6:96521904..96521988 26863196 MeRIP-seq:(Medium) rs1227136672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4904183,Human_RBP_ID_8905865,Human_RBP_ID_9309378,Human_RBP_ID_18425472 Human_Splice_Rec_795903,Human_Splice_Rec_795905 102541 RMVar_ID_102541 Human_SNP_ID_288331631 m1A Human chr6 - 96542837 96542837 96542837 GCATTACCTAACTAAATCATCATTTTTATAAAATAATGACACTATATTGTTGTATTTAACTTTAC GCATTACCTAACTAAATCATCATTTTTATAAAGTAATGACACTATATTGTTGTATTTAACTTTAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:96542835..96542973 26863196 MeRIP-seq:(Medium) rs565392252 Functional Loss SNV dbSNP153 33..33 33 - - - 102542 RMVar_ID_102542 Human_SNP_ID_288413267 m1A Human chr6 - 96892812 96892812 96892812 ATTACTTTGGAAGAATGTGTAGAGTGAGAAGAAGGCCTGGGCACTCTTAAATGTCACACACTGAC ATTACTTTGGAAGAATGTGTAGAGTGAGAAGACGGCCTGGGCACTCTTAAATGTCACACACTGAC T G NDUFAF4 Ensembl:ENSG00000123545 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:96892804..96893168;chr6:96892803..96893129 26863196 MeRIP-seq:(Medium) rs73758054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7649017 102543 RMVar_ID_102543 Human_SNP_ID_288414478 m1A Human chr6 + 96897788 96897788 96897788 TCTCTAGGTTGAAATTCCTGATACCGCGAATCACTAGTGCTCCCATCTCCTCATAACATTATGCG TCTCTAGGTTGAAATTCCTGATACCGCGAATCGCTAGTGCTCCCATCTCCTCATAACATTATGCG A G lnc-KLHL32-6 RNACentral:URS00008BE80F lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:96897738..96897830 26863196 MeRIP-seq:(Medium) rs755386760 Functional Loss SNV dbSNP153 33..33 33 - - - 102544 RMVar_ID_102544 Human_SNP_ID_288414479 m1A Human chr6 + 96897788 96897788 96897788 TCTCTAGGTTGAAATTCCTGATACCGCGAATCACTAGTGCTCCCATCTCCTCATAACATTATGCG TCTCTAGGTTGAAATTCCTGATACCGCGAATCTCTAGTGCTCCCATCTCCTCATAACATTATGCG A T lnc-KLHL32-6 RNACentral:URS00008BE80F lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:96897738..96897830 26863196 MeRIP-seq:(Medium) rs755386760 Functional Loss SNV dbSNP153 33..33 33 - - - 102545 RMVar_ID_102545 Human_SNP_ID_288481441 m1A Human chr6 - 97191098 97191098 97191098 TGGGGGCAAAATGGATAAGTAAACATGAAATCAAAGCAAGAAGTAGCAGACAAATAAAAACAGGA TGGGGGCAAAATGGATAAGTAAACATGAAATCGAAGCAAGAAGTAGCAGACAAATAAAAACAGGA T C MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:97191058..97191134 26863196 MeRIP-seq:(Medium) rs1277821516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15536,RMVar_hsa_circ_48700,RMVar_hsa_circ_35131,RMVar_hsa_circ_100542,RMVar_hsa_circ_240402,RMVar_hsa_circ_104194,RMVar_hsa_circ_111578,RMVar_hsa_circ_240403,RMVar_hsa_circ_269385,RMVar_hsa_circ_346850,RMVar_hsa_circ_240405 102546 RMVar_ID_102546 Human_SNP_ID_288488404 m1A Human chr6 - 97219993 97219993 97219993 GGGAATGGAAGTAATTGTCAAAATCAAGAGTCAGAAGTGGTCAGTGTTGGTAATAGTAGACATAG GGGAATGGAAGTAATTGTCAAAATCAAGAGTCTGAAGTGGTCAGTGTTGGTAATAGTAGACATAG T A MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:97219972..97220055 26863196 MeRIP-seq:(Medium) rs1490618621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15916485 RMVar_hsa_circ_15536,RMVar_hsa_circ_48700,RMVar_hsa_circ_35131,RMVar_hsa_circ_100542,RMVar_hsa_circ_240402,RMVar_hsa_circ_104194,RMVar_hsa_circ_111578,RMVar_hsa_circ_240403,RMVar_hsa_circ_269385,RMVar_hsa_circ_346850,RMVar_hsa_circ_240405 102547 RMVar_ID_102547 Human_SNP_ID_288873675 m1A Human chr6 - 98834625 98834625 98834625 TCTCCTCCTCTCCCTCCTTCTCGCTCTCGCTCACTCTCTGACTAGCTCGGCGCTCCCCCCTCTCC TCTCCTCCTCTCCCTCCTTCTCGCTCTCGCTCTCTCTCTGACTAGCTCGGCGCTCCCCCCTCTCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:98834578..98834841 26863196 MeRIP-seq:(Medium) rs1248047945 Functional Loss SNV dbSNP153 33..33 33 - - - 102548 RMVar_ID_102548 Human_SNP_ID_288873714 m1A Human chr6 + 98834704 98834704 98834704 GGGCGGGAGGCGGCGGCGGCGGCAGCAGCAGCAGTAATAGCAGGAGCAGCAACAGAAGGCGTCGG GGGCGGGAGGCGGCGGCGGCGGCAGCAGCAGCCGTAATAGCAGGAGCAGCAACAGAAGGCGTCGG A C POU3F2 Ensembl:ENSG00000184486 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:98834586..98835040 26863196 MeRIP-seq:(Medium) rs186667950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1142908 102549 RMVar_ID_102549 Human_SNP_ID_288873727 m1A Human chr6 + 98834765 98834763 98834765 TCGGAGCGGGCGTCGGAGCTGCCCGCTGTGGGAGAGAGAGGAGACAGAAAGAGCGAGCGAGGAGA TCGGAGCGGGCGTCGGAGCTGCCCGCTGTGG__GAGAGAGGAGACAGAAAGAGCGAGCGAGGAGA GGA G POU3F2 Ensembl:ENSG00000184486 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:98834563..98834918 26863196 MeRIP-seq:(Medium) rs1412804648 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4916982,Human_RBP_ID_17069978 102550 RMVar_ID_102550 Human_SNP_ID_288873870 m1A Human chr6 - 98835095 98835074 98835095 CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCACCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCC_____________________GTGGGACAGCGC CGGCGGCGGCGGCGGGGGCGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr6:98835069..98835289;chr6:98834995..98835211;chr6:98834992..98835130;chr6:98835004..98835200;chr6:98835082..98835154 26863196 MeRIP-seq:(Medium) rs1377146803 Functional Loss DEL dbSNP153 33..53 33 - - - 102551 RMVar_ID_102551 Human_SNP_ID_288873872 m1A Human chr6 - 98835095 98835077 98835095 CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCACCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCC__________________GCCGTGGGACAGCGC CGGCGGCGGCGGGGGCGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr6:98835069..98835289;chr6:98834995..98835211;chr6:98834992..98835130;chr6:98835004..98835200;chr6:98835082..98835154 26863196 MeRIP-seq:(Medium) rs757811015 Functional Loss DEL dbSNP153 33..50 33 - - - 102552 RMVar_ID_102552 Human_SNP_ID_288873885 m1A Human chr6 - 98835095 98835095 98835095 CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCACCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCGCCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr6:98835069..98835289;chr6:98834995..98835211;chr6:98834992..98835130;chr6:98835004..98835200;chr6:98835082..98835154 26863196 MeRIP-seq:(Medium) rs1280489469 Functional Loss SNV dbSNP153 33..33 33 - - - 102553 RMVar_ID_102553 Human_SNP_ID_288873886 m1A Human chr6 - 98835095 98835095 98835095 CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCACCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC CCGCCGCCGCCCCCGCCCCCCCCGCCGCCGCCCCCGCCCCCGCCGCCGCCGCCGTGGGACAGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr6:98835069..98835289;chr6:98834995..98835211;chr6:98834992..98835130;chr6:98835004..98835200;chr6:98835082..98835154 26863196 MeRIP-seq:(Medium) rs1280489469 Functional Loss SNV dbSNP153 33..33 33 - - - 102554 RMVar_ID_102554 Human_SNP_ID_288874120 m1A Human chr6 + 98835568 98835568 98835568 GCCACACCATGCCGACCACCACCCGCACCCGCACTCGCACCCACACCAGCAGCCGCCGCCCCCGC GCCACACCATGCCGACCACCACCCGCACCCGCCCTCGCACCCACACCAGCAGCCGCCGCCCCCGC A C POU3F2 Ensembl:ENSG00000184486 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:98835487..98835601 26863196 MeRIP-seq:(Medium) rs1406095183 Functional Loss SNV dbSNP153 33..33 33 - - - 102555 RMVar_ID_102555 Human_SNP_ID_288991891 m1A Human chr6 + 99327795 99327795 99327795 AACCTGATTCTCCTCACCCAAGCCAGAATCCCAGGAGTTTTTCTTCACTGACCCCTCTCCCTCAC AACCTGATTCTCCTCACCCAAGCCAGAATCCCCGGAGTTTTTCTTCACTGACCCCTCTCCCTCAC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:99327781..99327883 26863196 MeRIP-seq:(Medium) rs58206007 Functional Loss SNV dbSNP153 33..33 33 - - - 102556 RMVar_ID_102556 Human_SNP_ID_288995297 m1A Human chr6 - 99343807 99343807 99343807 AGACAGAGCTAGAGAGAGAGCATCCAGAAGGCAGGTTCCATGGCATTACAGGTGAAAGAAGGGTT AGACAGAGCTAGAGAGAGAGCATCCAGAAGGCGGGTTCCATGGCATTACAGGTGAAAGAAGGGTT T C FAXC Ensembl:ENSG00000146267 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:99343805..99343894 26863196 MeRIP-seq:(Medium) rs890969650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8228,RMVar_hsa_circ_33599,RMVar_hsa_circ_342758,RMVar_hsa_circ_240479 102557 RMVar_ID_102557 Human_SNP_ID_288995374 m1A Human chr6 - 99344262 99344262 99344262 CCGAGGAGTGGGGTATGAGTGGGGCTGTGTGGAATGATGAGCTTGCAGGGATGAGACCATATCTC CCGAGGAGTGGGGTATGAGTGGGGCTGTGTGGGATGATGAGCTTGCAGGGATGAGACCATATCTC T C FAXC Ensembl:ENSG00000146267 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:99344260..99344376 26863196 MeRIP-seq:(Medium) rs1269698156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24178352 RMVar_hsa_circ_8228,RMVar_hsa_circ_33599,RMVar_hsa_circ_342758,RMVar_hsa_circ_240479 102558 RMVar_ID_102558 Human_SNP_ID_288996632 m1A Human chr6 + 99349457 99349443 99349457 GAAGGGGCCGGCGCGGCCCGGCGCGGGCTCAGAGGCGCGCGGAGGGCGCGGGCGGCGCGGGCGGC GAAGGGGCCGGCGCGGCCC______________GGCGCGCGGAGGGCGCGGGCGGCGCGGGCGGC CGGCGCGGGCTCAGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:99349408..99349625 26863196 MeRIP-seq:(Medium) rs1004656192 Functional Loss DEL dbSNP153 20..33 33 - - - 102559 RMVar_ID_102559 Human_SNP_ID_288996704 m1A Human chr6 - 99349554 99349554 99349554 GGCCCCGCCGGCCAGGCCCGCCGTCCGCGGCCAGTGCCCTTCCTCCTCCTCCTCCTCTGCCGCCG GGCCCCGCCGGCCAGGCCCGCCGTCCGCGGCCGGTGCCCTTCCTCCTCCTCCTCCTCTGCCGCCG T C FAXC Ensembl:ENSG00000146267 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:99349504..99349635 26863196 MeRIP-seq:(Medium) rs1427517719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240479 102560 RMVar_ID_102560 Human_SNP_ID_289007728 m1A Human chr6 + 99394155 99394155 99394155 CCCCAGCACTCTTAAAAACCAACCCCCGGAGGAGCCCAGCTTACGGCCACTCCACATCGCGACAA CCCCAGCACTCTTAAAAACCAACCCCCGGAGGCGCCCAGCTTACGGCCACTCCACATCGCGACAA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:99383808..99394155 26863410 MeRIP-seq:(Medium) rs763042659 Functional Loss SNV dbSNP153 33..33 33 - - - 102561 RMVar_ID_102561 Human_SNP_ID_289007729 m1A Human chr6 + 99394155 99394155 99394155 CCCCAGCACTCTTAAAAACCAACCCCCGGAGGAGCCCAGCTTACGGCCACTCCACATCGCGACAA CCCCAGCACTCTTAAAAACCAACCCCCGGAGGGGCCCAGCTTACGGCCACTCCACATCGCGACAA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:99383808..99394155 26863410 MeRIP-seq:(Medium) rs763042659 Functional Loss SNV dbSNP153 33..33 33 - - - 102562 RMVar_ID_102562 Human_SNP_ID_289009556 m1A Human chr6 - 99400914 99400911 99400914 GAAGTATAGATAAAGATAGGAAAAAGAAAGACAAAGAAAGGGAACGTGAACAGGATAAAAGAAAA GAAGTATAGATAAAGATAGGAAAAAGAAAGAC___GAAAGGGAACGTGAACAGGATAAAAGAAAA CTTT C PNISR Ensembl:ENSG00000132424 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:99400767..99401252;chr6:99400751..99401200 26863196 MeRIP-seq:(Medium) rs777588737 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_81694,Human_RBP_ID_3025677,Human_RBP_ID_10308405,Human_RBP_ID_23067060,Human_RBP_ID_26036894 102563 RMVar_ID_102563 Human_SNP_ID_289009558 m1A Human chr6 - 99400914 99400911 99400915 GAAGTATAGATAAAGATAGGAAAAAGAAAGACAAAGAAAGGGAACGTGAACAGGATAAAAGAAAA GAAGTATAGATAAAGATAGGAAAAAGAAAGA____GAAAGGGAACGTGAACAGGATAAAAGAAAA CTTTG C PNISR Ensembl:ENSG00000132424 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:99400767..99401252;chr6:99400751..99401200 26863196 MeRIP-seq:(Medium) rs1562223680 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_81694,Human_RBP_ID_3025677,Human_RBP_ID_10308405,Human_RBP_ID_23067060,Human_RBP_ID_26036894 102564 RMVar_ID_102564 Human_SNP_ID_289009559 m1A Human chr6 - 99400916 99400913 99400917 TCGAAGTATAGATAAAGATAGGAAAAAGAAAGACAAAGAAAGGGAACGTGAACAGGATAAAAGAA TCGAAGTATAGATAAAGATAGGAAAAAGAAA____AAGAAAGGGAACGTGAACAGGATAAAAGAA TTGTC T PNISR Ensembl:ENSG00000132424 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:99400726..99401257 26863196 MeRIP-seq:(Medium) rs751290688 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_81694,Human_RBP_ID_671055,Human_RBP_ID_3025677,Human_RBP_ID_10308405,Human_RBP_ID_23067060,Human_RBP_ID_26036894 102565 RMVar_ID_102565 Human_SNP_ID_289010085 m1A Human chr6 + 99402624 99402624 99402624 AGCTTCCTGTTTTTGCCGGATTCGATGCCGTAATTCTTCATCATCAGTGTCAGATGACTCAGATC AGCTTCCTGTTTTTGCCGGATTCGATGCCGTAGTTCTTCATCATCAGTGTCAGATGACTCAGATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:99402573..99402678 26863196 MeRIP-seq:(Medium) rs367828524 Functional Loss SNV dbSNP153 33..33 33 - - - 102566 RMVar_ID_102566 Human_SNP_ID_289010478 m1A Human chr6 + 99404254 99404251 99404254 GATAAGTGGTAAACTAAAAATTGTAGGTAGATAATTCAAAATTCATTAGTCAAAATAAACTGTAT GATAAGTGGTAAACTAAAAATTGTAGGTAG___ATTCAAAATTCATTAGTCAAAATAAACTGTAT GATA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:99404244..99404345 32194978 MeRIP-seq:(Medium) rs1174763565 Functional Loss DEL dbSNP153 31..33 33 - - - 102567 RMVar_ID_102567 Human_SNP_ID_289037743 m1A Human chr6 - 99515353 99515353 99515353 TGAGAACGCGGCGCTTTGGTCGCAGCGGCGGTATGGTCGCCGCAGTTTCTCGGTCTTCGCTTCGG TGAGAACGCGGCGCTTTGGTCGCAGCGGCGGTTTGGTCGCCGCAGTTTCTCGGTCTTCGCTTCGG T A USP45 Ensembl:ENSG00000123552 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:99515337..99515404 26863196 MeRIP-seq:(Medium) rs1384454960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4902989 RMVar_hsa_circ_268630,RMVar_hsa_circ_267188 102568 RMVar_ID_102568 Human_SNP_ID_289037744 m1A Human chr6 - 99515353 99515353 99515353 TGAGAACGCGGCGCTTTGGTCGCAGCGGCGGTATGGTCGCCGCAGTTTCTCGGTCTTCGCTTCGG TGAGAACGCGGCGCTTTGGTCGCAGCGGCGGTGTGGTCGCCGCAGTTTCTCGGTCTTCGCTTCGG T C USP45 Ensembl:ENSG00000123552 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:99515337..99515404 26863196 MeRIP-seq:(Medium) rs1384454960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4902989 RMVar_hsa_circ_268630,RMVar_hsa_circ_267188 102569 RMVar_ID_102569 Human_SNP_ID_289039229 m1A Human chr6 + 99521075 99521075 99521075 GTGGTCACTAGCGCGGCGGCCGCCGGCCCGCAATGGTGCTACCCTGGTTGCTGCTCGAGACTGCG GTGGTCACTAGCGCGGCGGCCGCCGGCCCGCAGTGGTGCTACCCTGGTTGCTGCTCGAGACTGCG A G TSTD3 Ensembl:ENSG00000279170 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:99521021..99521184 26863196 MeRIP-seq:(Medium) rs538288096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671155,Human_RBP_ID_4904192,Human_RBP_ID_18425706 Human_Splice_Rec_797389,Human_Splice_Rec_797395,Human_Splice_Rec_797403,Human_Splice_Rec_797411,Human_Splice_Rec_797417,Human_Splice_Rec_797423 102570 RMVar_ID_102570 Human_SNP_ID_289049899 m1A Human chr6 + 99568531 99568531 99568531 TGGGAGCTCTGCCAAAAGTTCCCTGCCATGGAACACAGCTTGCCCTGATAAAAAAGCACCAGCCG TGGGAGCTCTGCCAAAAGTTCCCTGCCATGGACCACAGCTTGCCCTGATAAAAAAGCACCAGCCG A C TSTD3 Ensembl:ENSG00000279170 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:99568496..99568696 32194978 MeRIP-seq:(Medium) rs1473573779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 102571 RMVar_ID_102571 Human_SNP_ID_289309345 m1A Human chr6 - 100625276 100625276 100625276 CCTGTTTTGATATTTGTCTCATCAAGACGTCAAACTCGTCTTACTGCTTTGGAATTGATCGCCTT CCTGTTTTGATATTTGTCTCATCAAGACGTCAGACTCGTCTTACTGCTTTGGAATTGATCGCCTT T C ASCC3 Ensembl:ENSG00000112249 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs778047681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2002766,Human_RBP_ID_4858199,Human_RBP_ID_8894769,Human_RBP_ID_9402487,Human_RBP_ID_24125207 Human_Splice_Rec_797922,Human_Splice_Rec_797923 Human_miRNA_ID_2198176,Human_miRNA_ID_2198407,Human_miRNA_ID_2430671 RMVar_hsa_circ_4092,RMVar_hsa_circ_80986,RMVar_hsa_circ_117155,RMVar_hsa_circ_240529,RMVar_hsa_circ_128129,RMVar_hsa_circ_102010,RMVar_hsa_circ_118845,RMVar_hsa_circ_240532,RMVar_hsa_circ_240533,RMVar_hsa_circ_240531,RMVar_hsa_circ_114243,RMVar_hsa_circ_19934,RMVar_hsa_circ_82741,RMVar_hsa_circ_91287,RMVar_hsa_circ_240536,RMVar_hsa_circ_350394,RMVar_hsa_circ_88960,RMVar_hsa_circ_66704,RMVar_hsa_circ_71928,RMVar_hsa_circ_240540,RMVar_hsa_circ_240541,RMVar_hsa_circ_240542,RMVar_hsa_circ_240539,RMVar_hsa_circ_296138,RMVar_hsa_circ_335008,RMVar_hsa_circ_22265,RMVar_hsa_circ_72548,RMVar_hsa_circ_41590,RMVar_hsa_circ_61162,RMVar_hsa_circ_83437,RMVar_hsa_circ_240544,RMVar_hsa_circ_5158,RMVar_hsa_circ_240543,RMVar_hsa_circ_240545,RMVar_hsa_circ_33713,RMVar_hsa_circ_25624,RMVar_hsa_circ_48719,RMVar_hsa_circ_55060,RMVar_hsa_circ_51826,RMVar_hsa_circ_277621,RMVar_hsa_circ_114540,RMVar_hsa_circ_265012,RMVar_hsa_circ_300001,RMVar_hsa_circ_366043,RMVar_hsa_circ_240548,RMVar_hsa_circ_327393,RMVar_hsa_circ_292512,RMVar_hsa_circ_117329,RMVar_hsa_circ_124703,RMVar_hsa_circ_63525,RMVar_hsa_circ_240549,RMVar_hsa_circ_240551,RMVar_hsa_circ_240552,RMVar_hsa_circ_240553,RMVar_hsa_circ_240550 102572 RMVar_ID_102572 Human_SNP_ID_289364992 m1A Human chr6 - 100859143 100859143 100859143 GGCTGGATGGAAAAGAGGAGGATGAGAAGATGAGCAGAGCTTCTGACAGATTCAGAGGACTAAGA GGCTGGATGGAAAAGAGGAGGATGAGAAGATGCGCAGAGCTTCTGACAGATTCAGAGGACTAAGA T G ASCC3 Ensembl:ENSG00000112249 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:100859106..100859234 26863196 MeRIP-seq:(Medium) rs1371625489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7508881,Human_RBP_ID_15579015,Human_RBP_ID_18449300,Human_RBP_ID_27827933 Human_Splice_Rec_798028 RMVar_hsa_circ_117155,RMVar_hsa_circ_240529,RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_117329,RMVar_hsa_circ_240553,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562,RMVar_hsa_circ_357001,RMVar_hsa_circ_9025,RMVar_hsa_circ_318511,RMVar_hsa_circ_240601,RMVar_hsa_circ_26493,RMVar_hsa_circ_292815,RMVar_hsa_circ_276824 102573 RMVar_ID_102573 Human_SNP_ID_289370018 m1A Human chr6 - 100881116 100881116 100881116 GTGGGAAGTTAAAGTAAAACCGAAAGGGAAGAAGGCGCGGTGGCAGGAGCTGACAGAGTGATGGG GTGGGAAGTTAAAGTAAAACCGAAAGGGAAGAGGGCGCGGTGGCAGGAGCTGACAGAGTGATGGG T C ASCC3 Ensembl:ENSG00000112249 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:100881009..100881282 26863196 MeRIP-seq:(Medium) rs760569545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4858317,Human_RBP_ID_5152223,Human_RBP_ID_15579342,Human_RBP_ID_24125438,Human_RBP_ID_27085847 Human_Splice_Rec_797865,Human_Splice_Rec_797949,Human_Splice_Rec_797987,Human_Splice_Rec_798011,Human_Splice_Rec_798017,Human_Splice_Rec_798023 RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562 102574 RMVar_ID_102574 Human_SNP_ID_289370051 m1A Human chr6 - 100881199 100881199 100881199 AGCGCGGCTTGGAGGGCGGACGGGGCGCGGCGATACAGCTGCCCGCTCGCATCTTTGGCCCTGCG AGCGCGGCTTGGAGGGCGGACGGGGCGCGGCGGTACAGCTGCCCGCTCGCATCTTTGGCCCTGCG T C ASCC3 Ensembl:ENSG00000112249 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:100881153..100881270 26863196 MeRIP-seq:(Medium) rs78881114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251275,Human_RBP_ID_841751,Human_RBP_ID_4905050,Human_RBP_ID_5304491,Human_RBP_ID_9309380,Human_RBP_ID_23120381 RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562 102575 RMVar_ID_102575 Human_SNP_ID_467898602 m1A Human chr11 - 57300021 57300021 57300021 TGCCCATTCCTGTGGGGTCCCTGGGTGAGGAGACGGCTGGAGCCCCACCATGCCCCAGGCTGCAG TGCCCATTCCTGTGGGGTCCCTGGGTGAGGAGGCGGCTGGAGCCCCACCATGCCCCAGGCTGCAG T C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57299728..57300034 26863196 MeRIP-seq:(Medium) rs1056667747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226640,Human_RBP_ID_5110745,Human_RBP_ID_5138543,Human_RBP_ID_5549394,Human_RBP_ID_17682054,Human_RBP_ID_17796966,Human_RBP_ID_18973611,Human_RBP_ID_22790565 Human_Splice_Rec_1239430,Human_Splice_Rec_1239452,Human_Splice_Rec_1239472,Human_Splice_Rec_1239482 Human_miRNA_ID_2973862,Human_miRNA_ID_3007048 RMVar_hsa_circ_83559,RMVar_hsa_circ_149729 102576 RMVar_ID_102576 Human_SNP_ID_467898857 m1A Human chr11 - 57301001 57301001 57301001 GCGCCCCCGGAATCGCTCAGCTGAGGAGGGAGAGCTGGCTGAGAGCAAGTCGAGCCAGAAGGAGT GCGCCCCCGGAATCGCTCAGCTGAGGAGGGAGGGCTGGCTGAGAGCAAGTCGAGCCAGAAGGAGT T C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57300951..57301074 26863196 MeRIP-seq:(Medium) rs745959121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1239448,Human_Splice_Rec_1239468,Human_Splice_Rec_1239478 RMVar_hsa_circ_83559,RMVar_hsa_circ_70749,RMVar_hsa_circ_149729 102577 RMVar_ID_102577 Human_SNP_ID_467899327 m1A Human chr11 + 57302519 57302519 57302519 GATCTGGCAGGAGGGCCTTGGGAGGGTCGCCGAGAAGTCTGTGCTGGCCCCTGATCGCTCCACCT GATCTGGCAGGAGGGCCTTGGGAGGGTCGCCGCGAAGTCTGTGCTGGCCCCTGATCGCTCCACCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57302461..57302662 26863196 MeRIP-seq:(Medium) rs1012053173 Functional Loss SNV dbSNP153 33..33 33 - - - 102578 RMVar_ID_102578 Human_SNP_ID_467900667 m1A Human chr11 - 57307444 57307442 57307444 AGGCATTTGGGATGGAGGAGGAGAAGGGAGAGAGGAAGATGGGCCCAGTGAGATGCCCAGGGGGA AGGCATTTGGGATGGAGGAGGAGAAGGGAGAG__GAAGATGGGCCCAGTGAGATGCCCAGGGGGA CCT C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57307276..57307538 26863196 MeRIP-seq:(Medium) rs1352420765 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2950,Human_RBP_ID_3384114,Human_RBP_ID_5235212,Human_RBP_ID_6078774,Human_RBP_ID_8175706,Human_RBP_ID_9414492,Human_RBP_ID_17067083,Human_RBP_ID_23508589 102579 RMVar_ID_102579 Human_SNP_ID_467901137 m1A Human chr11 - 57309022 57309022 57309022 AATCGGAGTTGGGGAGAAGGACTGGACTTCTGATGTTAATGTGAAGAGCAAAGATTTGGCTGAGG AATCGGAGTTGGGGAGAAGGACTGGACTTCTGTTGTTAATGTGAAGAGCAAAGATTTGGCTGAGG T A TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57308651..57310400 26863196 MeRIP-seq:(Medium) rs1430154343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2271781,Human_RBP_ID_8352795,Human_RBP_ID_8769808,Human_RBP_ID_9254571,Human_RBP_ID_9275559,Human_RBP_ID_22895022 102580 RMVar_ID_102580 Human_SNP_ID_467901138 m1A Human chr11 + 57309024 57309024 57309024 TCAGCCAAATCTTTGCTCTTCACATTAACATCAGAAGTCCAGTCCTTCTCCCCAACTCCGATTCC TCAGCCAAATCTTTGCTCTTCACATTAACATCGGAAGTCCAGTCCTTCTCCCCAACTCCGATTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57308494..57310425 26863196 MeRIP-seq:(Medium) rs1328158604 Functional Loss SNV dbSNP153 33..33 33 - - - 102581 RMVar_ID_102581 Human_SNP_ID_467901166 m1A Human chr11 + 57309087 57309087 57309087 CCCCCCGGCTCTTCAGACCCTCCACTTTCCAAACAGCCGGTCAGGTTCATGTCTCTCAAGCTCAG CCCCCCGGCTCTTCAGACCCTCCACTTTCCAACCAGCCGGTCAGGTTCATGTCTCTCAAGCTCAG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:57308626..57310100 26863196 MeRIP-seq:(Medium) rs1407028431 Functional Loss SNV dbSNP153 33..33 33 - - - 102582 RMVar_ID_102582 Human_SNP_ID_467901665 m1A Human chr11 - 57310381 57310381 57310381 CCCAGGTCTCGGAGAGAGGGACTGGACCAGCAAGTATGGGCAAGGAGCAGGGGAAGGGAGCACCA CCCAGGTCTCGGAGAGAGGGACTGGACCAGCACGTATGGGCAAGGAGCAGGGGAAGGGAGCACCA T G TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:57310330..57310531 32194978 MeRIP-seq:(Medium) rs150510361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6078787,Human_RBP_ID_27412093 Human_miRNA_ID_1092537 102583 RMVar_ID_102583 Human_SNP_ID_467902381 m1A Human chr11 - 57312763 57312763 57312763 TGTTCTCTTTGCTGATGCCCCTGAGCCTGGACAGGCACTGCCTGTTGAGGAGGAGGCCGTGACCC TGTTCTCTTTGCTGATGCCCCTGAGCCTGGACGGGCACTGCCTGTTGAGGAGGAGGCCGTGACCC T C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57312713..57312866 26863196 MeRIP-seq:(Medium) rs754082213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8773448,Human_RBP_ID_9275563,Human_RBP_ID_22034417,Human_RBP_ID_26891435 102584 RMVar_ID_102584 Human_SNP_ID_467902746 m1A Human chr11 - 57313586 57313586 57313586 CTGCCGAGGGGGCTCCAGAGGCCCCCAGACCCAGCAGCCCACCCCCTGAGGTCTTGGAGCCCCAT CTGCCGAGGGGGCTCCAGAGGCCCCCAGACCCGGCAGCCCACCCCCTGAGGTCTTGGAGCCCCAT T C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:57313537..57313700 26863196 MeRIP-seq:(Medium) rs1316793828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_473440,Human_miRNA_ID_1701279 102585 RMVar_ID_102585 Human_SNP_ID_467902803 m1A Human chr11 + 57313674 57313674 57313674 CGGGAGCCCTCGTCAGGCAGGGCTGCACTTGGAGCTGATGGAGTCACAGCGGGGCAGGGAGAAGC CGGGAGCCCTCGTCAGGCAGGGCTGCACTTGGTGCTGATGGAGTCACAGCGGGGCAGGGAGAAGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:57313626..57313700 26863196 MeRIP-seq:(Medium) rs767596560 Functional Loss SNV dbSNP153 33..33 33 - - - 102586 RMVar_ID_102586 Human_SNP_ID_467903229 m1A Human chr11 - 57315172 57315172 57315172 TGATGCAGAGGTTGCAGCCACTGGTAAGGATGAGGTCTAGGGTGTGACCTTGAGAGGATGGGTCG TGATGCAGAGGTTGCAGCCACTGGTAAGGATGCGGTCTAGGGTGTGACCTTGAGAGGATGGGTCG T G TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57315170..57315390 26863196 MeRIP-seq:(Medium) rs980931369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2505 102587 RMVar_ID_102587 Human_SNP_ID_467903390 m1A Human chr11 - 57315785 57315785 57315785 GAAGGGGAGGCAGAGTGCTTGGGCTCCCATGCAGGAAGTAGGTGGTGTGTGTGTGTGTGGCGGTG GAAGGGGAGGCAGAGTGCTTGGGCTCCCATGCGGGAAGTAGGTGGTGTGTGTGTGTGTGGCGGTG T C TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57315782..57315886 26863196 MeRIP-seq:(Medium) rs868049724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5234987 102588 RMVar_ID_102588 Human_SNP_ID_467904647 m1A Human chr11 + 57320556 57320555 57320556 GCTTGCTGCCACCATAGGGCTGGGGTCCTGCCAGCATGTTCATCTTCCTGGCAGAAGGCAACTCA GCTTGCTGCCACCATAGGGCTGGGGTCCTGCC_GCATGTTCATCTTCCTGGCAGAAGGCAACTCA CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57320506..57320594 26863196 MeRIP-seq:(Medium) rs774112650 Functional Loss DEL dbSNP153 33..33 33 - - - 102589 RMVar_ID_102589 Human_SNP_ID_467905903 m1A Human chr11 - 57324888 57324888 57324888 CGGCGGCGGTAGCAGCGGCGGCGGCGGCGGGGACTGGCATCGGGGCCCCGAGCCGAGCGGAGCCG CGGCGGCGGTAGCAGCGGCGGCGGCGGCGGGGTCTGGCATCGGGGCCCCGAGCCGAGCGGAGCCG T A TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:57324816..57324917;chr11:57324820..57324925;chr11:57324799..57324925 26863196 MeRIP-seq:(Medium) rs1424623653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184038,Human_RBP_ID_18432791 Human_Splice_Rec_1239419,Human_Splice_Rec_1239431 102590 RMVar_ID_102590 Human_SNP_ID_467906361 m1A Human chr11 - 57326462 57326460 57326463 CACCTTTGGTTTTCAGGACTCTGAAGAAGAAGAACTAGCCAGTACTCCCCCCAGCTCAGAGGACT CACCTTTGGTTTTCAGGACTCTGAAGAAGAA___CTAGCCAGTACTCCCCCCAGCTCAGAGGACT GTTC G SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57326232..57326495 26863196 MeRIP-seq:(Medium) rs764601446 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_30713,Human_RBP_ID_226645,Human_RBP_ID_870808,Human_RBP_ID_1457474,Human_RBP_ID_1779906,Human_RBP_ID_6078805,Human_RBP_ID_9362235,Human_RBP_ID_11642244,Human_RBP_ID_19051560,Human_RBP_ID_22570994,Human_RBP_ID_23508632,Human_RBP_ID_26318311 Human_Splice_Rec_1239510,Human_Splice_Rec_1239542 Human_miRNA_ID_1993554 RMVar_hsa_circ_84817,RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_113781,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149744,RMVar_hsa_circ_149745,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732 102591 RMVar_ID_102591 Human_SNP_ID_467906508 m1A Human chr11 - 57326879 57326877 57326880 CTCTTCCCTCTTGCCAATACAGGGACAAGTCAAAGAAGAAGAAGAAAGTAAAGGTAAAGATGGAA CTCTTCCCTCTTGCCAATACAGGGACAAGTC___GAAGAAGAAGAAAGTAAAGGTAAAGATGGAA CTTT C SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57326432..57326956 26863196 MeRIP-seq:(Medium) rs749275379 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_30714,Human_RBP_ID_193346,Human_RBP_ID_870810,Human_RBP_ID_1779911,Human_RBP_ID_9362239,Human_RBP_ID_17648679,Human_RBP_ID_22034426,Human_RBP_ID_24542648,Human_RBP_ID_26318315,Human_RBP_ID_27803427 Human_Splice_Rec_1239540,Human_Splice_Rec_1239556 RMVar_hsa_circ_84817,RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_113781,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_94097,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149744,RMVar_hsa_circ_149745,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_149746 102592 RMVar_ID_102592 Human_SNP_ID_467906508 m1A Human chr11 - 57326880 57326877 57326880 CCTCTTCCCTCTTGCCAATACAGGGACAAGTCAAAGAAGAAGAAGAAAGTAAAGGTAAAGATGGA CCTCTTCCCTCTTGCCAATACAGGGACAAGTC___GAAGAAGAAGAAAGTAAAGGTAAAGATGGA CTTT C SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:57326664..57326928;chr11:57326686..57326903;chr11:57326701..57326956 26863196 MeRIP-seq:(Medium) rs749275379 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_30714,Human_RBP_ID_193346,Human_RBP_ID_870810,Human_RBP_ID_1779911,Human_RBP_ID_9362239,Human_RBP_ID_17648679,Human_RBP_ID_22034426,Human_RBP_ID_22537401,Human_RBP_ID_24542648,Human_RBP_ID_26318315,Human_RBP_ID_27803427 Human_Splice_Rec_1239540,Human_Splice_Rec_1239556 RMVar_hsa_circ_84817,RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_113781,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_94097,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149744,RMVar_hsa_circ_149745,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_149746 102593 RMVar_ID_102593 Human_SNP_ID_467906510 m1A Human chr11 - 57326879 57326879 57326879 CTCTTCCCTCTTGCCAATACAGGGACAAGTCAAAGAAGAAGAAGAAAGTAAAGGTAAAGATGGAA CTCTTCCCTCTTGCCAATACAGGGACAAGTCAGAGAAGAAGAAGAAAGTAAAGGTAAAGATGGAA T C SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57326432..57326956 26863196 MeRIP-seq:(Medium) rs1407284220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30714,Human_RBP_ID_193346,Human_RBP_ID_870810,Human_RBP_ID_1779911,Human_RBP_ID_9362239,Human_RBP_ID_17648679,Human_RBP_ID_22034426,Human_RBP_ID_24542648,Human_RBP_ID_26318315,Human_RBP_ID_27803427 Human_Splice_Rec_1239540,Human_Splice_Rec_1239556 RMVar_hsa_circ_84817,RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_113781,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_94097,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149744,RMVar_hsa_circ_149745,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_149746 102594 RMVar_ID_102594 Human_SNP_ID_467906673 m1A Human chr11 + 57327465 57327465 57327465 AAGACTCGCCTCGGCCCCCTTCATATTCTTTCATGGCTTTTTCATAGTCCCTCCTGGCATCCTCA AAGACTCGCCTCGGCCCCCTTCATATTCTTTCCTGGCTTTTTCATAGTCCCTCCTGGCATCCTCA A C AP000781.1 Ensembl:ENSG00000254662 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:57327426..57327583 26863196 MeRIP-seq:(Medium) rs1188248956 Functional Loss SNV dbSNP153 33..33 33 - - - 102595 RMVar_ID_102595 Human_SNP_ID_467906674 m1A Human chr11 + 57327465 57327465 57327465 AAGACTCGCCTCGGCCCCCTTCATATTCTTTCATGGCTTTTTCATAGTCCCTCCTGGCATCCTCA AAGACTCGCCTCGGCCCCCTTCATATTCTTTCGTGGCTTTTTCATAGTCCCTCCTGGCATCCTCA A G AP000781.1 Ensembl:ENSG00000254662 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:57327426..57327583 26863196 MeRIP-seq:(Medium) rs1188248956 Functional Loss SNV dbSNP153 33..33 33 - - - 102596 RMVar_ID_102596 Human_SNP_ID_467906677 m1A Human chr11 + 57327476 57327476 57327476 CGGCCCCCTTCATATTCTTTCATGGCTTTTTCATAGTCCCTCCTGGCATCCTCAGCCTTGCGATC CGGCCCCCTTCATATTCTTTCATGGCTTTTTCGTAGTCCCTCCTGGCATCCTCAGCCTTGCGATC A G AP000781.1 Ensembl:ENSG00000254662 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:57327404..57327542;chr11:57327403..57327904;chr11:57327389..57327902 26863196 MeRIP-seq:(Medium) rs1026059948 Functional Loss SNV dbSNP153 33..33 33 - - - 102597 RMVar_ID_102597 Human_SNP_ID_467925012 m1A Human chr11 - 57398352 57398352 57398352 ACAGTGCATCAGAGGTGGAGGAGGGTGGTAAGACTGGAGGCAGGGAAAGTAATTTGGGAGCCACT ACAGTGCATCAGAGGTGGAGGAGGGTGGTAAGGCTGGAGGCAGGGAAAGTAATTTGGGAGCCACT T C AP000781.2 Ensembl:ENSG00000254979 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57398326..57398429 26863196 MeRIP-seq:(Medium) rs1326506788 Functional Loss SNV dbSNP153 33..33 33 - - - 102598 RMVar_ID_102598 Human_SNP_ID_467932404 m1A Human chr11 + 57426326 57426326 57426326 GTAGCTCTCTGGTTGTTTCAGGCCTGGGCAAAAACCATCAGCGGGTGATTCTCTGGATCCTGTAG GTAGCTCTCTGGTTGTTTCAGGCCTGGGCAAACACCATCAGCGGGTGATTCTCTGGATCCTGTAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57426144..57426400 26863196 MeRIP-seq:(Medium) rs1318307190 Functional Loss SNV dbSNP153 33..33 33 - - - 102599 RMVar_ID_102599 Human_SNP_ID_467932489 m1A Human chr11 - 57426644 57426644 57426644 GTTGAGTTGCTGTCATTATTTTAGGGGACGGTATTCAGAATTCGAGCGCAGGAGCTCCGCTTCTC GTTGAGTTGCTGTCATTATTTTAGGGGACGGTGTTCAGAATTCGAGCGCAGGAGCTCCGCTTCTC T C SLC43A3 Ensembl:ENSG00000134802 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:57426576..57426675 26863196 MeRIP-seq:(Medium) rs964805515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2271851,Human_RBP_ID_4184847,Human_RBP_ID_11642632,Human_RBP_ID_19054776 Human_Splice_Rec_1239708,Human_Splice_Rec_1239709,Human_Splice_Rec_1239734,Human_Splice_Rec_1239735,Human_Splice_Rec_1239760,Human_Splice_Rec_1239761,Human_Splice_Rec_1239785,Human_Splice_Rec_1239818,Human_Splice_Rec_1239819,Human_Splice_Rec_1239844,Human_Splice_Rec_1239845,Human_Splice_Rec_1239886,Human_Splice_Rec_1239887,Human_Splice_Rec_1239897,Human_Splice_Rec_1239908,Human_Splice_Rec_1239909,Human_Splice_Rec_1239922,Human_Splice_Rec_1239923,Human_Splice_Rec_1239952,Human_Splice_Rec_1239953,Human_Splice_Rec_1239958,Human_Splice_Rec_1239959,Human_Splice_Rec_1239963,Human_Splice_Rec_1239968,Human_Splice_Rec_1239969,Human_Splice_Rec_1239975,Human_Splice_Rec_1239978,Human_Splice_Rec_1239979,Human_Splice_Rec_1239983 RMVar_hsa_circ_63092,RMVar_hsa_circ_38126,RMVar_hsa_circ_366261,RMVar_hsa_circ_30822 102600 RMVar_ID_102600 Human_SNP_ID_467932554 m1A Human chr11 - 57426944 57426944 57426944 CAGGCTGGAGCGGGGTGCGGAGGCTGGCGGGGAGCGGCCCCCGGAGGCTTTCCTGGTAGAAGTTG CAGGCTGGAGCGGGGTGCGGAGGCTGGCGGGGGGCGGCCCCCGGAGGCTTTCCTGGTAGAAGTTG T C SLC43A3 Ensembl:ENSG00000134802 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:57426941..57427100 26863196 MeRIP-seq:(Medium) rs918501105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259401,Human_RBP_ID_864964,Human_RBP_ID_5341323,Human_RBP_ID_19054778,Human_RBP_ID_22034438,Human_RBP_ID_22641174,Human_RBP_ID_22736376,Human_RBP_ID_26775766,Human_RBP_ID_27836317 Human_Splice_Rec_1239707,Human_Splice_Rec_1239843,Human_Splice_Rec_1239981 102601 RMVar_ID_102601 Human_SNP_ID_467940779 m1A Human chr11 + 57461540 57461540 57461540 AAGCTCAAAGGAGGAGGGAGATGGAGCGGGGGAGGGGGAGAAGGAATAAAGGTTAGATGGGAAAA AAGCTCAAAGGAGGAGGGAGATGGAGCGGGGGGGGGGGAGAAGGAATAAAGGTTAGATGGGAAAA A G RTN4RL2 Ensembl:ENSG00000186907 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57461532..57461897 26863196 MeRIP-seq:(Medium) rs1452096028 Functional Loss SNV dbSNP153 33..33 33 - - - 102602 RMVar_ID_102602 Human_SNP_ID_467944585 m1A Human chr11 - 57476988 57476988 57476988 AGGGAGGCAGCAAGGCCAGGGAAGGTGGGGCGACTGGGGCCGGAGCCGCAGCCCCGGGTGGACGG AGGGAGGCAGCAAGGCCAGGGAAGGTGGGGCGCCTGGGGCCGGAGCCGCAGCCCCGGGTGGACGG T G AP002893.1 Ensembl:ENSG00000255301 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57476367..57477100 26863196 MeRIP-seq:(Medium) rs1396735561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_806888,Human_RBP_ID_3385025,Human_RBP_ID_8229526,Human_RBP_ID_9414877,Human_RBP_ID_26775596 102603 RMVar_ID_102603 Human_SNP_ID_467950985 m1A Human chr11 - 57501172 57501167 57501172 CTGGGGATCCTCATGGACCGCTTTGGCCCCCGACCCGTGCGGCTGGTTGGCAGGTGAGGTGGCTG CTGGGGATCCTCATGGACCGCTTTGGCCCCCG_____TGCGGCTGGTTGGCAGGTGAGGTGGCTG ACGGGT A SLC43A1 Ensembl:ENSG00000149150 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:57501152..57501285 26863196 MeRIP-seq:(Medium) rs1403108480 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_4184049,Human_RBP_ID_18971967 Human_Splice_Rec_1240003,Human_Splice_Rec_1240031,Human_Splice_Rec_1240055,Human_Splice_Rec_1240087,Human_Splice_Rec_1240099,Human_Splice_Rec_1240111,Human_Splice_Rec_1240121 RMVar_hsa_circ_70359,RMVar_hsa_circ_373537,RMVar_hsa_circ_149768,RMVar_hsa_circ_94502,RMVar_hsa_circ_149771,RMVar_hsa_circ_86727,RMVar_hsa_circ_31946,RMVar_hsa_circ_149778,RMVar_hsa_circ_45251,RMVar_hsa_circ_55147,RMVar_hsa_circ_47590,RMVar_hsa_circ_266806 102604 RMVar_ID_102604 Human_SNP_ID_467957561 m1A Human chr11 + 57528754 57528754 57528754 CAGGCCCAGAGCTCTGCTGCACCCTCTTCATCAGCTCTTCATCCTGCATAGACAACTCTGTCAAC CAGGCCCAGAGCTCTGCTGCACCCTCTTCATCGGCTCTTCATCCTGCATAGACAACTCTGTCAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57528656..57528754 32194978 MeRIP-seq:(Medium) rs762310126 Functional Loss SNV dbSNP153 33..33 33 - - - 102605 RMVar_ID_102605 Human_SNP_ID_467957916 m1A Human chr11 - 57530233 57530233 57530233 GGTGGGTGCTGATGGTGATGTCTGCTCCCAGGATTAGGAGGCCAGAAGGAGATCCCTTCCACGGT GGTGGGTGCTGATGGTGATGTCTGCTCCCAGGTTTAGGAGGCCAGAAGGAGATCCCTTCCACGGT T A TIMM10 Ensembl:ENSG00000134809 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57530184..57530296 26863196 MeRIP-seq:(Medium) rs1288558552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184853,Human_RBP_ID_5461123,Human_RBP_ID_26803457 Human_Splice_Rec_1240134,Human_Splice_Rec_1240140 102606 RMVar_ID_102606 Human_SNP_ID_467957918 m1A Human chr11 - 57530236 57530236 57530236 GGCGGTGGGTGCTGATGGTGATGTCTGCTCCCAGGATTAGGAGGCCAGAAGGAGATCCCTTCCAC GGCGGTGGGTGCTGATGGTGATGTCTGCTCCCTGGATTAGGAGGCCAGAAGGAGATCCCTTCCAC T A TIMM10 Ensembl:ENSG00000134809 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57530203..57530309 26863196 MeRIP-seq:(Medium) rs113138790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1240140 102607 RMVar_ID_102607 Human_SNP_ID_467957919 m1A Human chr11 - 57530236 57530236 57530236 GGCGGTGGGTGCTGATGGTGATGTCTGCTCCCAGGATTAGGAGGCCAGAAGGAGATCCCTTCCAC GGCGGTGGGTGCTGATGGTGATGTCTGCTCCCGGGATTAGGAGGCCAGAAGGAGATCCCTTCCAC T C TIMM10 Ensembl:ENSG00000134809 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57530203..57530309 26863196 MeRIP-seq:(Medium) rs113138790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1240140 102608 RMVar_ID_102608 Human_SNP_ID_467958018 m1A Human chr11 + 57530697 57530697 57530697 TGGGACGGATCACAATGCCCACGGAGACCCCAACTTCTGACAAATACTATAACGTTACCCGCCTC TGGGACGGATCACAATGCCCACGGAGACCCCAGCTTCTGACAAATACTATAACGTTACCCGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57530083..57530750 26863196 MeRIP-seq:(Medium) rs1251540976 Functional Loss SNV dbSNP153 33..33 33 - - - 102609 RMVar_ID_102609 Human_SNP_ID_467963567 m1A Human chr11 - 57552330 57552330 57552330 CCTAACTCATGTTCTGACCCTCTGTGCACTGGATCCTCGGCATAGCGGACGGACACACCTCATGG CCTAACTCATGTTCTGACCCTCTGTGCACTGGGTCCTCGGCATAGCGGACGGACACACCTCATGG T C UBE2L6 Ensembl:ENSG00000156587 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57552154..57560450 32194978 MeRIP-seq:(Medium) rs779524373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109294,Human_RBP_ID_5138873,Human_RBP_ID_9004282,Human_RBP_ID_22434367 Human_miRNA_ID_85760,Human_miRNA_ID_310726,Human_miRNA_ID_1078134 RMVar_hsa_circ_149784,RMVar_hsa_circ_95722,RMVar_hsa_circ_117765,RMVar_hsa_circ_100222,RMVar_hsa_circ_149785,RMVar_hsa_circ_149786 102610 RMVar_ID_102610 Human_SNP_ID_467964192 m1A Human chr11 - 57554625 57554625 57554625 AGACTGGAGCTTGACCCCTTTTCTCTCTGCACAGGACCAACCTCCCTACCACCTGAAAGCCTTCA AGACTGGAGCTTGACCCCTTTTCTCTCTGCACGGGACCAACCTCCCTACCACCTGAAAGCCTTCA T C UBE2L6 Ensembl:ENSG00000156587 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57554529..57554692 26863196 MeRIP-seq:(Medium) rs1213256468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117765,RMVar_hsa_circ_149786,RMVar_hsa_circ_302242 102611 RMVar_ID_102611 Human_SNP_ID_467979356 m1A Human chr11 + 57614702 57614702 57614702 CTGCCACCTCCTGCCTCAGGTGTCCGCTATCCACCAAAAGGGCTCCCTGAGGGTCTGGGCAAGGG CTGCCACCTCCTGCCTCAGGTGTCCGCTATCCGCCAAAAGGGCTCCCTGAGGGTCTGGGCAAGGG A G SERPING1 Ensembl:ENSG00000149131 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:57614654..57614759 32194978 MeRIP-seq:(Medium) rs1565174235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17234936,Human_RBP_ID_17467098,Human_RBP_ID_17649555 Human_miRNA_ID_2001774,Human_miRNA_ID_2003158 RMVar_hsa_circ_108027,RMVar_hsa_circ_149789 102612 RMVar_ID_102612 Human_SNP_ID_467985359 m1A Human chr11 - 57639403 57639401 57639404 CCCCTCCTCGCAGCCATGGCGACGGGAGGAGGAGACCAGGAGGGTCCTGAAAGCCATGTTCTGTG CCCCTCCTCGCAGCCATGGCGACGGGAGGAG___ACCAGGAGGGTCCTGAAAGCCATGTTCTGTG TCTC T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:57639354..57639486 26863196 MeRIP-seq:(Medium) rs960708147 Functional Loss DEL dbSNP153 32..34 33 - - - 102613 RMVar_ID_102613 Human_SNP_ID_467985360 m1A Human chr11 - 57639403 57639403 57639403 CCCCTCCTCGCAGCCATGGCGACGGGAGGAGGAGACCAGGAGGGTCCTGAAAGCCATGTTCTGTG CCCCTCCTCGCAGCCATGGCGACGGGAGGAGGGGACCAGGAGGGTCCTGAAAGCCATGTTCTGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:57639354..57639486 26863196 MeRIP-seq:(Medium) rs1428796387 Functional Loss SNV dbSNP153 33..33 33 - - - 102614 RMVar_ID_102614 Human_SNP_ID_467985487 m1A Human chr11 - 57639848 57639848 57639848 CAGGGGGCAGAGGGGCAAAGATAAGGCTGCACAGCAAGCTTCAGGGAGGCCAGGGGAAGATTCTT CAGGGGGCAGAGGGGCAAAGATAAGGCTGCACGGCAAGCTTCAGGGAGGCCAGGGGAAGATTCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57639745..57639865 26863196 MeRIP-seq:(Medium) rs1439856561 Functional Loss SNV dbSNP153 33..33 33 - - - 102615 RMVar_ID_102615 Human_SNP_ID_467988202 m1A Human chr11 + 57649784 57649784 57649784 TCACTCTTCTCTCTTCTCTTTCCGCTCCTTCAATTGGGAAGGGGATGGGGGTGGGTGGGGGGAGG TCACTCTTCTCTCTTCTCTTTCCGCTCCTTCAGTTGGGAAGGGGATGGGGGTGGGTGGGGGGAGG A G AP000662.1,CLP1 Ensembl:ENSG00000254602,Ensembl:ENSG00000172409 lincRNA,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57649747..57649885 26863196 MeRIP-seq:(Medium) rs1210576587 Functional Loss SNV dbSNP153 33..33 33 - - - 102616 RMVar_ID_102616 Human_SNP_ID_468001256 m1A Human chr11 + 57700819 57700819 57700819 AAAATAACTTGGCCTAGCTCAAACAATATTGGATAATCCCCTCCTTGGGGGAGAGGGATTAGAGT AAAATAACTTGGCCTAGCTCAAACAATATTGGGTAATCCCCTCCTTGGGGGAGAGGGATTAGAGT A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:57700776..57700921 26863196 MeRIP-seq:(Medium) rs1464572656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4163354,Human_RBP_ID_5139083,Human_RBP_ID_11643349,Human_RBP_ID_17682076,Human_RBP_ID_17797109,Human_RBP_ID_26408463 RMVar_hsa_circ_107222,RMVar_hsa_circ_149793 102617 RMVar_ID_102617 Human_SNP_ID_468004461 m1A Human chr11 - 57712084 57712084 57712084 GGCTTCGGACCAGGAAAGCCTCCACCCCCGCCACCGCCTCCTGCGGGCGGGGGACCCGGCACGGC GGCTTCGGACCAGGAAAGCCTCCACCCCCGCCGCCGCCTCCTGCGGGCGGGGGACCCGGCACGGC T C MED19 Ensembl:ENSG00000156603 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57712034..57712198 26863196 MeRIP-seq:(Medium) rs796092878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4191103 102618 RMVar_ID_102618 Human_SNP_ID_468004490 m1A Human chr11 + 57712160 57712160 57712160 GGGGCGGTGGTGGGTCAGCCTGAGCCCCAAACAGTGCCGTGAAATTCTCCATCGTACCCTCCGCC GGGGCGGTGGTGGGTCAGCCTGAGCCCCAAACCGTGCCGTGAAATTCTCCATCGTACCCTCCGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57711931..57712274 26863196 MeRIP-seq:(Medium) rs1249605807 Functional Loss SNV dbSNP153 33..33 33 - - - 102619 RMVar_ID_102619 Human_SNP_ID_468004496 m1A Human chr11 + 57712171 57712171 57712171 GGGTCAGCCTGAGCCCCAAACAGTGCCGTGAAATTCTCCATCGTACCCTCCGCCCCGGCGCTGTC GGGTCAGCCTGAGCCCCAAACAGTGCCGTGAAGTTCTCCATCGTACCCTCCGCCCCGGCGCTGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57711970..57712247 26863196 MeRIP-seq:(Medium) rs1189994876 Functional Loss SNV dbSNP153 33..33 33 - - - 102620 RMVar_ID_102620 Human_SNP_ID_468004817 m1A Human chr11 + 57712758 57712758 57712758 CCTACTCGTGAGGAAACTGCCGCCGCTCTGCCACGGTCTGCCCACCCAACGCGAAGACGGTAACC CCTACTCGTGAGGAAACTGCCGCCGCTCTGCCGCGGTCTGCCCACCCAACGCGAAGACGGTAACC A G AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57712601..57712834 26863196 MeRIP-seq:(Medium) rs1370870229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397700,Human_RBP_ID_9363603,Human_RBP_ID_22432905 Human_Splice_Rec_1240507,Human_Splice_Rec_1240543,Human_Splice_Rec_1240581,Human_Splice_Rec_1240621,Human_Splice_Rec_1240659,Human_Splice_Rec_1240673,Human_Splice_Rec_1240679,Human_Splice_Rec_1240691,Human_Splice_Rec_1240697,Human_Splice_Rec_1240707,Human_Splice_Rec_1240713,Human_Splice_Rec_1240723,Human_Splice_Rec_1240737 Human_miRNA_ID_2027303,Human_miRNA_ID_2027304,Human_miRNA_ID_2873400,Human_miRNA_ID_2873401,Human_miRNA_ID_2981363,Human_miRNA_ID_2981364 RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 102621 RMVar_ID_102621 Human_SNP_ID_468013416 m1A Human chr11 - 57741569 57741569 57741569 AGCCATGGCGCCTAGAGCCCGGCCGAGAATGCAGCGGGACTGGTGGGTGGGGGGCGGAGACGCGA AGCCATGGCGCCTAGAGCCCGGCCGAGAATGCGGCGGGACTGGTGGGTGGGGGGCGGAGACGCGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:57741495..57741742 32194978 MeRIP-seq:(Medium) rs979775218 Functional Loss SNV dbSNP153 33..33 33 - - - 102622 RMVar_ID_102622 Human_SNP_ID_468013475 m1A Human chr11 + 57741646 57741646 57741646 AAGCGTAAGGCTGAGGCCGCGGTGGTCGCCGTAGCCGAGAAGCGAGAGAAGCTGGCGAACGGCGG AAGCGTAAGGCTGAGGCCGCGGTGGTCGCCGTTGCCGAGAAGCGAGAGAAGCTGGCGAACGGCGG A T AP001931.2,SELENOH Ensembl:ENSG00000288534,Ensembl:ENSG00000211450 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:57741544..57741791 26863410 MeRIP-seq:(Medium) rs375720963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227330,Human_RBP_ID_397725,Human_RBP_ID_4184057,Human_RBP_ID_18416554,Human_RBP_ID_22432906,Human_RBP_ID_24890339 Human_Splice_Rec_1240739,Human_Splice_Rec_1240745,Human_Splice_Rec_1240751,Human_Splice_Rec_1240753,Human_Splice_Rec_1240757 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957 102623 RMVar_ID_102623 Human_SNP_ID_468013506 m1A Human chr11 + 57741693 57741693 57741693 GAAGCTGGCGAACGGCGGGGAGGGAATGGAGGAGGCGACCGTTGTTATCGAGCATTGGTGAGGGG GAAGCTGGCGAACGGCGGGGAGGGAATGGAGGCGGCGACCGTTGTTATCGAGCATTGGTGAGGGG A C AP001931.2,SELENOH Ensembl:ENSG00000288534,Ensembl:ENSG00000211450 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57741397..57741989 26863196 MeRIP-seq:(Medium) rs1266778248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809071,Human_RBP_ID_4184867,Human_RBP_ID_8229072,Human_RBP_ID_22432906 Human_Splice_Rec_1240739,Human_Splice_Rec_1240745,Human_Splice_Rec_1240751,Human_Splice_Rec_1240753,Human_Splice_Rec_1240757 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957 102624 RMVar_ID_102624 Human_SNP_ID_468013655 m1A Human chr11 + 57741889 57741889 57741889 GCTGCGCCTGGAGGCCCCAGAGCTTCCAGTAAAGGTGAACCCGACGAAGCCCCGGAGGGGCAGCT GCTGCGCCTGGAGGCCCCAGAGCTTCCAGTAAGGGTGAACCCGACGAAGCCCCGGAGGGGCAGCT A G AP001931.2,SELENOH,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000211450,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,CDS,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57741840..57741988 32194978 MeRIP-seq:(Medium) rs1297921948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397728,Human_RBP_ID_4163433,Human_RBP_ID_23113171 Human_Splice_Rec_1240740,Human_Splice_Rec_1240741,Human_Splice_Rec_1240746,Human_Splice_Rec_1240747,Human_Splice_Rec_1240752,Human_Splice_Rec_1240754,Human_Splice_Rec_1240755,Human_Splice_Rec_1240758,Human_Splice_Rec_1240759,Human_Splice_Rec_1240763,Human_Splice_Rec_1240767 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957 102625 RMVar_ID_102625 Human_SNP_ID_468013687 m1A Human chr11 + 57741925 57741925 57741925 GAACCCGACGAAGCCCCGGAGGGGCAGCTTCGAGGTGACGCTGCTGCGCCCGGACGGCAGCAGTA GAACCCGACGAAGCCCCGGAGGGGCAGCTTCGTGGTGACGCTGCTGCGCCCGGACGGCAGCAGTA A T AP001931.2,SELENOH,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000211450,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,CDS,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57741875..57741994 26863196 MeRIP-seq:(Medium) rs185768359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397729,Human_RBP_ID_4163434,Human_RBP_ID_17805086,Human_RBP_ID_23113171 Human_Splice_Rec_1240741,Human_Splice_Rec_1240747,Human_Splice_Rec_1240755,Human_Splice_Rec_1240759,Human_Splice_Rec_1240763,Human_Splice_Rec_1240767 GWAS_ID_13424 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957 102626 RMVar_ID_102626 Human_SNP_ID_468013828 m1A Human chr11 + 57742201 57742198 57742201 CCCTGAGCCTCAAGAGGTGGTGGAAGAGTTGAAGAAGTACCTGTCGTAGGGAGATTTGGGTAGAA CCCTGAGCCTCAAGAGGTGGTGGAAGAGTT___GAAGTACCTGTCGTAGGGAGATTTGGGTAGAA TGAA T AP001931.2,SELENOH,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000211450,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57742104..57742215 26863196 MeRIP-seq:(Medium) rs767623062 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_397732,Human_RBP_ID_5110415,Human_RBP_ID_5138548,Human_RBP_ID_8352936,Human_RBP_ID_9004304,Human_RBP_ID_17062218,Human_RBP_ID_17649074,Human_RBP_ID_17682081,Human_RBP_ID_17804562,Human_RBP_ID_23207295,Human_RBP_ID_23508951 Human_Splice_Rec_1240742,Human_Splice_Rec_1240743,Human_Splice_Rec_1240748,Human_Splice_Rec_1240749,Human_Splice_Rec_1240756,Human_Splice_Rec_1240760,Human_Splice_Rec_1240761,Human_Splice_Rec_1240764,Human_Splice_Rec_1240765,Human_Splice_Rec_1240768,Human_Splice_Rec_1240769,Human_Splice_Rec_1240787 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957 102627 RMVar_ID_102627 Human_SNP_ID_468013850 m1A Human chr11 - 57742241 57742241 57742241 CGCGCCCCCCACTTCCCATTTCAAACCTCAGCATGAGGGCTTCTACCCAAATCTCCCTACGACAG CGCGCCCCCCACTTCCCATTTCAAACCTCAGCGTGAGGGCTTCTACCCAAATCTCCCTACGACAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57742191..57742290 26863196 MeRIP-seq:(Medium) rs1343697103 Functional Loss SNV dbSNP153 33..33 33 - - - 102628 RMVar_ID_102628 Human_SNP_ID_468019068 m1A Human chr11 + 57761883 57761879 57761883 TTCCATTTTAGGTGTTGGATCTGAGGGGGAAAAAAAAGAGAGAGGGAGAGAGAGAGAAAGAAGAG TTCCATTTTAGGTGTTGGATCTGAGGGGG____AAAAGAGAGAGGGAGAGAGAGAGAAAGAAGAG GAAAA G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57761833..57761936 26863196 MeRIP-seq:(Medium) rs1164486569 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_2958,Human_RBP_ID_31904,Human_RBP_ID_4163448,Human_RBP_ID_8774080,Human_RBP_ID_8940540,Human_RBP_ID_17067084,Human_RBP_ID_18416555,Human_RBP_ID_21966487,Human_RBP_ID_24916980,Human_RBP_ID_27804455 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 102629 RMVar_ID_102629 Human_SNP_ID_468019069 m1A Human chr11 + 57761883 57761879 57761883 TTCCATTTTAGGTGTTGGATCTGAGGGGGAAAAAAAAGAGAGAGGGAGAGAGAGAGAAAGAAGAG TTCCATTTTAGGTGTTGGATCTGAGGGGGAAA_AAAAGAGAGAGGGAGAGAGAGAGAAAGAAGAG GAAAA GAAA AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57761833..57761936 26863196 MeRIP-seq:(Medium) rs1164486569 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2958,Human_RBP_ID_31904,Human_RBP_ID_4163448,Human_RBP_ID_8774080,Human_RBP_ID_8940540,Human_RBP_ID_17067084,Human_RBP_ID_18416555,Human_RBP_ID_21966487,Human_RBP_ID_24916980,Human_RBP_ID_27804455 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 102630 RMVar_ID_102630 Human_SNP_ID_468028487 m1A Human chr11 - 57801850 57801850 57801850 GGCAGCTCTGGCTGTCTCCAATTAGGAGGTGGAGGCCCTCCTTTGCGCAGGCTATCCAAGCTTGC GGCAGCTCTGGCTGTCTCCAATTAGGAGGTGGCGGCCCTCCTTTGCGCAGGCTATCCAAGCTTGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57801801..57801850 32194978 MeRIP-seq:(Medium) rs982617816 Functional Loss SNV dbSNP153 33..33 33 - - - 102631 RMVar_ID_102631 Human_SNP_ID_468028509 m1A Human chr11 - 57801926 57801926 57801926 GCATAAGTGTTGCAGGTATGCAGCTGCATTGGACTTGACAGCATCCAAGCGGAATCCAAGCATGG GCATAAGTGTTGCAGGTATGCAGCTGCATTGGCCTTGACAGCATCCAAGCGGAATCCAAGCATGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57801876..57803790 32194978 MeRIP-seq:(Medium) rs751036815 Functional Loss SNV dbSNP153 33..33 33 - - - 102632 RMVar_ID_102632 Human_SNP_ID_468219050 m1A Human chr11 - 58578746 58578745 58578746 AGAAATCGCACCTCTTTCCCCGCCTCACGCAAACCCTAGACTGGCTGCGCGCGCACCTGCCTCCC AGAAATCGCACCTCTTTCCCCGCCTCACGCAA_CCCTAGACTGGCTGCGCGCGCACCTGCCTCCC GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:58578695..58578821 32194978 MeRIP-seq:(Medium) rs545620982 Functional Loss DEL dbSNP153 33..33 33 - - - 102633 RMVar_ID_102633 Human_SNP_ID_468219051 m1A Human chr11 - 58578746 58578746 58578746 AGAAATCGCACCTCTTTCCCCGCCTCACGCAAACCCTAGACTGGCTGCGCGCGCACCTGCCTCCC AGAAATCGCACCTCTTTCCCCGCCTCACGCAATCCCTAGACTGGCTGCGCGCGCACCTGCCTCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:58578695..58578821 32194978 MeRIP-seq:(Medium) rs1555013632 Functional Loss SNV dbSNP153 33..33 33 - - - 102634 RMVar_ID_102634 Human_SNP_ID_468219286 m1A Human chr11 - 58579177 58579173 58579177 CCCGCCCCCTCGCCTCCCGAAGCCTGCGGCTCACTCTCACCCTGCGCTCCTCTTTCCCCCCTCCC CCCGCCCCCTCGCCTCCCGAAGCCTGCGGCTC____TCACCCTGCGCTCCTCTTTCCCCCCTCCC AGAGT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:58579126..58579350 26863196 MeRIP-seq:(Medium) rs1231019695 Functional Loss DEL dbSNP153 33..36 33 - - - 102635 RMVar_ID_102635 Human_SNP_ID_468219287 m1A Human chr11 - 58579177 58579177 58579177 CCCGCCCCCTCGCCTCCCGAAGCCTGCGGCTCACTCTCACCCTGCGCTCCTCTTTCCCCCCTCCC CCCGCCCCCTCGCCTCCCGAAGCCTGCGGCTCTCTCTCACCCTGCGCTCCTCTTTCCCCCCTCCC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:58579126..58579350 26863196 MeRIP-seq:(Medium) rs576710868 Functional Loss SNV dbSNP153 33..33 33 - - - 102636 RMVar_ID_102636 Human_SNP_ID_468219297 m1A Human chr11 + 58579200 58579200 58579200 GGGTGAGAGTGAGCCGCAGGCTTCGGGAGGCGAGGGGGCGGGGGGAGCAGCGCCGAGGCCGCCGC GGGTGAGAGTGAGCCGCAGGCTTCGGGAGGCGGGGGGGCGGGGGGAGCAGCGCCGAGGCCGCCGC A G ZFP91-CNTF,ZFP91 Ensembl:ENSG00000255073,Ensembl:ENSG00000186660 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:58579151..58579330 26863196 MeRIP-seq:(Medium) rs1413031232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2959,Human_RBP_ID_193706,Human_RBP_ID_1064929,Human_RBP_ID_3384116,Human_RBP_ID_5313599,Human_RBP_ID_5342288,Human_RBP_ID_8940541,Human_RBP_ID_9275588,Human_RBP_ID_9322036,Human_RBP_ID_9414493,Human_RBP_ID_18410483,Human_RBP_ID_18416556,Human_RBP_ID_22426091,Human_RBP_ID_22433532,Human_RBP_ID_22708736,Human_RBP_ID_24529523,Human_RBP_ID_26318348 102637 RMVar_ID_102637 Human_SNP_ID_468227680 m1A Human chr11 + 58611656 58611656 58611656 GAAAATCAGGGAAGGTAAAAGAAGAGAAGGAGAAGAAGGAAATTAAAGTGGAAGTAGAGGTGGAG GAAAATCAGGGAAGGTAAAAGAAGAGAAGGAGGAGAAGGAAATTAAAGTGGAAGTAGAGGTGGAG A G ZFP91-CNTF,ZFP91 Ensembl:ENSG00000255073,Ensembl:ENSG00000186660 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:58610905..58612350 26863196 MeRIP-seq:(Medium) rs1439906064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6079858,Human_RBP_ID_17797241,Human_RBP_ID_18525851,Human_RBP_ID_23113068,Human_RBP_ID_24542339,Human_RBP_ID_26319825 Human_Splice_Rec_1242133,Human_Splice_Rec_1242151,Human_Splice_Rec_1242169 RMVar_hsa_circ_32508,RMVar_hsa_circ_23374,RMVar_hsa_circ_362133,RMVar_hsa_circ_308297,RMVar_hsa_circ_338786,RMVar_hsa_circ_115509,RMVar_hsa_circ_125769,RMVar_hsa_circ_149836,RMVar_hsa_circ_149837,RMVar_hsa_circ_149838 102638 RMVar_ID_102638 Human_SNP_ID_468230083 m1A Human chr11 + 58620579 58620579 58620579 TATGCTTCAGAGAATTTAGGCAAACACTGGCCATGGCCGTGGGAGTACTGGGAGTAAAATAAAAA TATGCTTCAGAGAATTTAGGCAAACACTGGCCGTGGCCGTGGGAGTACTGGGAGTAAAATAAAAA A G ZFP91-CNTF,ZFP91 Ensembl:ENSG00000255073,Ensembl:ENSG00000186660 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:58620529..58620611 26863196 MeRIP-seq:(Medium) rs961931549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397889,Human_RBP_ID_987387,Human_RBP_ID_6080012,Human_RBP_ID_11647535,Human_RBP_ID_17797290,Human_RBP_ID_22491337,Human_RBP_ID_27618348 Human_miRNA_ID_1809097 RMVar_hsa_circ_23374 102639 RMVar_ID_102639 Human_SNP_ID_468364517 m1A Human chr11 + 59145199 59145199 59145199 AGAAAGTGGGGGTTGGGGTGCGGAGAAGCAGGAAGAGAGGGAGAGTGAAGGAGGGGAGGAAAGGG AGAAAGTGGGGGTTGGGGTGCGGAGAAGCAGGGAGAGAGGGAGAGTGAAGGAGGGGAGGAAAGGG A G FAM111A Ensembl:ENSG00000166801 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59144798..59145452 26863196 MeRIP-seq:(Medium) rs144510750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102994,RMVar_hsa_circ_93537,RMVar_hsa_circ_149845,RMVar_hsa_circ_149846 102640 RMVar_ID_102640 Human_SNP_ID_468371257 m1A Human chr11 + 59172349 59172349 59172349 CATGAAGCGACTCGACCCCACAGAGCAGCGGCAGCAGCAGCGGACCCCGGCGGCGGCGGCGGCGC CATGAAGCGACTCGACCCCACAGAGCAGCGGCGGCAGCAGCGGACCCCGGCGGCGGCGGCGGCGC A G DTX4 Ensembl:ENSG00000110042 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59172164..59172748 26863196 MeRIP-seq:(Medium) rs1443693074 Functional Loss SNV dbSNP153 33..33 33 - - - 102641 RMVar_ID_102641 Human_SNP_ID_468371294 m1A Human chr11 + 59172488 59172475 59172489 CTGAGGCTGCCCGGGGCGGCGGGGCGCGGGGCAGGGGGCGCGGTCGAGGCCCGGAGGCGGCGGCG CTGAGGCTGCCCGGGGCGGC______________GGGGCGCGGTCGAGGCCCGGAGGCGGCGGCG CGGGGCGCGGGGCAG C DTX4 Ensembl:ENSG00000110042 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:59172372..59172591 26863196 MeRIP-seq:(Medium) rs1488788989 Functional Loss DEL dbSNP153 21..34 33 - - - 102642 RMVar_ID_102642 Human_SNP_ID_468371295 m1A Human chr11 + 59172488 59172479 59172488 CTGAGGCTGCCCGGGGCGGCGGGGCGCGGGGCAGGGGGCGCGGTCGAGGCCCGGAGGCGGCGGCG CTGAGGCTGCCCGGGGCGGCGGGG_________GGGGGCGCGGTCGAGGCCCGGAGGCGGCGGCG GCGCGGGGCA G DTX4 Ensembl:ENSG00000110042 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:59172372..59172591 26863196 MeRIP-seq:(Medium) rs1565213978 Functional Loss DEL dbSNP153 25..33 33 - - - 102643 RMVar_ID_102643 Human_SNP_ID_468470363 m1A Human chr11 - 59550644 59550644 59550644 GTCTGCTTTACACGCAGAAGGTCCTGGGTTCGAGCCCCAGTGGAACCATGAGATGTTACCTAGCG GTCTGCTTTACACGCAGAAGGTCCTGGGTTCGGGCCCCAGTGGAACCATGAGATGTTACCTAGCG T C tRNA-Val-TAC-1-1 RNACentral:URS000070B37B tRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1270892622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1457713,Human_RBP_ID_1780160,Human_RBP_ID_8246370,Human_RBP_ID_8353113,Human_RBP_ID_11648077,Human_RBP_ID_18174127,Human_RBP_ID_18206005,Human_RBP_ID_18609064,Human_RBP_ID_23124459 102644 RMVar_ID_102644 Human_SNP_ID_468474034 m1A Human chr11 + 59560480 59560480 59560480 ACCATTATGCCGTGAACTAACAGGCAAGGTGCAAGGTGGTGAACGAGTTCCTGGGCTCTTCTTTT ACCATTATGCCGTGAACTAACAGGCAAGGTGCCAGGTGGTGAACGAGTTCCTGGGCTCTTCTTTT A C lnc-OR4D9-1-001 RNACentral:URS0000D59B37 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59560473..59560578 26863196 MeRIP-seq:(Medium) rs1170822944 Functional Loss SNV dbSNP153 33..33 33 - - - 102645 RMVar_ID_102645 Human_SNP_ID_468475575 m1A Human chr11 - 59566283 59566283 59566283 CAGTTAACAGGGTCAACACCCTGTGGGTTCTCACGCGGGCTGGGGCAGTTAAGGGAAACCTTATC CAGTTAACAGGGTCAACACCCTGTGGGTTCTCCCGCGGGCTGGGGCAGTTAAGGGAAACCTTATC T G LINC02739 Ensembl:ENSG00000255008 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59566271..59566379 26863196 MeRIP-seq:(Medium) rs1217091052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22162744 102646 RMVar_ID_102646 Human_SNP_ID_468475614 m1A Human chr11 - 59566349 59566349 59566349 CAGCGCTTCCGTTTTAGGCGTTAGTCATCACTACATGTGATTTCTGCAGTTAACAGGGTCTTTCT CAGCGCTTCCGTTTTAGGCGTTAGTCATCACTGCATGTGATTTCTGCAGTTAACAGGGTCTTTCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:59566271..59566400 26863196 MeRIP-seq:(Medium) rs540075659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23124494 102647 RMVar_ID_102647 Human_SNP_ID_468475615 m1A Human chr11 - 59566349 59566349 59566349 CAGCGCTTCCGTTTTAGGCGTTAGTCATCACTACATGTGATTTCTGCAGTTAACAGGGTCTTTCT CAGCGCTTCCGTTTTAGGCGTTAGTCATCACTCCATGTGATTTCTGCAGTTAACAGGGTCTTTCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:59566271..59566400 26863196 MeRIP-seq:(Medium) rs540075659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23124494 102648 RMVar_ID_102648 Human_SNP_ID_468475660 m1A Human chr11 - 59566395 59566395 59566395 GTTAGACTGAAGATCTAAAGGTCCCTGGTTCAATCCCGGGTTTCGGCAGCGCTTCCGTTTTAGGC GTTAGACTGAAGATCTAAAGGTCCCTGGTTCAGTCCCGGGTTTCGGCAGCGCTTCCGTTTTAGGC T C TRF-GAA1-1,tRNA-Phe-GAA-2-1,TRF-GAA2-1,TRF-GAA1-1:2,TRF-GAA1-1:3 RNACentral:URS0000632456,RNACentral:URS00003A0C47,RNACentral:URS000064A2A2,RNACentral:URS00006A7E04,RNACentral:URS00006D05AC tRNA,tRNA,tRNA,tRNA,tRNA intron,intron,intron,intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs867118415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397939,Human_RBP_ID_1462487,Human_RBP_ID_6115859,Human_RBP_ID_8246387,Human_RBP_ID_8353142,Human_RBP_ID_9004415,Human_RBP_ID_17351208,Human_RBP_ID_18609090,Human_RBP_ID_19699985,Human_RBP_ID_22031952,Human_RBP_ID_22162746,Human_RBP_ID_22792679,Human_RBP_ID_22895805,Human_RBP_ID_23124495,Human_RBP_ID_23509522 102649 RMVar_ID_102649 Human_SNP_ID_468486557 m1A Human chr11 + 59610384 59610384 59610384 TCCCCAGGCAGGTGTTCTTTGTTCCTGACCTGACTCTGCCAGCATCTTCACAGCTTTGGCCTTGG TCCCCAGGCAGGTGTTCTTTGTTCCTGACCTGTCTCTGCCAGCATCTTCACAGCTTTGGCCTTGG A T AP000442.1 Ensembl:ENSG00000255139 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:59610382..59615495 32194978 MeRIP-seq:(Medium) rs1455063424 Functional Loss SNV dbSNP153 33..33 33 - - - 102650 RMVar_ID_102650 Human_SNP_ID_468498007 m1A Human chr11 + 59655500 59655500 59655500 CACAATCAAGAGACTTGGCTGATAACTGATAAACAGTGGCGTTGATTTTGTATACCTTAGGTTTT CACAATCAAGAGACTTGGCTGATAACTGATAACCAGTGGCGTTGATTTTGTATACCTTAGGTTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59655497..59655661 26863196 MeRIP-seq:(Medium) rs966550219 Functional Loss SNV dbSNP153 33..33 33 - - - 102651 RMVar_ID_102651 Human_SNP_ID_468498008 m1A Human chr11 + 59655500 59655500 59655500 CACAATCAAGAGACTTGGCTGATAACTGATAAACAGTGGCGTTGATTTTGTATACCTTAGGTTTT CACAATCAAGAGACTTGGCTGATAACTGATAAGCAGTGGCGTTGATTTTGTATACCTTAGGTTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59655497..59655661 26863196 MeRIP-seq:(Medium) rs966550219 Functional Loss SNV dbSNP153 33..33 33 - - - 102652 RMVar_ID_102652 Human_SNP_ID_468498043 m1A Human chr11 - 59655573 59655573 59655573 GCCTTCTTTAGTGCTCCACCCTCCGCTACACCACCTCCACAGCAGCACCCTCCTGGCCCAGGACC GCCTTCTTTAGTGCTCCACCCTCCGCTACACCGCCTCCACAGCAGCACCCTCCTGGCCCAGGACC T C PATL1 Ensembl:ENSG00000166889 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:59655491..59655662 26863196 MeRIP-seq:(Medium) rs775290637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17235191,Human_RBP_ID_17350148 Human_Splice_Rec_1242729 RMVar_hsa_circ_26011,RMVar_hsa_circ_94208,RMVar_hsa_circ_149864,RMVar_hsa_circ_149865,RMVar_hsa_circ_126477,RMVar_hsa_circ_90026,RMVar_hsa_circ_149866 102653 RMVar_ID_102653 Human_SNP_ID_468501409 m1A Human chr11 - 59669002 59669002 59669002 CCCCACGCACGCTCCGGCGTACGGCGGCGGCCAGGGGTCGCGAGCCGGTGGAGGACCCGCGCGCG CCCCACGCACGCTCCGGCGTACGGCGGCGGCCGGGGGTCGCGAGCCGGTGGAGGACCCGCGCGCG T C PATL1 Ensembl:ENSG00000166889 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:59668955..59669086;chr11:59668961..59669077 26863196 MeRIP-seq:(Medium) rs933980498 Functional Loss SNV dbSNP153 33..33 33 - - - 102654 RMVar_ID_102654 Human_SNP_ID_468521984 m1A Human chr11 + 59755458 59755458 59755458 GGCTCCCGTGGCCTCGGACGCTCCTCCTAGCTAGCGGCCGCCGCCCGCCGCCGCCTGCGCCTCCA GGCTCCCGTGGCCTCGGACGCTCCTCCTAGCTGGCGGCCGCCGCCCGCCGCCGCCTGCGCCTCCA A G STX3 Ensembl:ENSG00000166900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59755425..59755515 26863196 MeRIP-seq:(Medium) rs904902620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4164111,Human_RBP_ID_5167528,Human_RBP_ID_9321408,Human_RBP_ID_18416821,Human_RBP_ID_27804475 102655 RMVar_ID_102655 Human_SNP_ID_468521991 m1A Human chr11 - 59755481 59755475 59755481 CGGGCCCGCCGGGGCGAAGGAGCTGGAGGCGCAGGCGGCGGCGGGCGGCGGCCGCTAGCTAGGAG CGGGCCCGCCGGGGCGAAGGAGCTGGAGGCGC______CGGCGGGCGGCGGCCGCTAGCTAGGAG GCCGCCT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:59755434..59755561 26863196 MeRIP-seq:(Medium) rs1243295643 Functional Loss DEL dbSNP153 33..38 33 - - - 102656 RMVar_ID_102656 Human_SNP_ID_468530761 m1A Human chr11 + 59792210 59792209 59792210 ACGCAGCAAAGGGCGAATCCAGCGGCAGCTCGAAATTAGTATGTACTTGAGGTTTGGCGTGTGCC ACGCAGCAAAGGGCGAATCCAGCGGCAGCTCG_AATTAGTATGTACTTGAGGTTTGGCGTGTGCC GA G STX3 Ensembl:ENSG00000166900 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:59792127..59793161 32194978 MeRIP-seq:(Medium) rs1263743043 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_808342 Human_Splice_Rec_1242769,Human_Splice_Rec_1242787,Human_Splice_Rec_1242805,Human_Splice_Rec_1242825,Human_Splice_Rec_1242845,Human_Splice_Rec_1242865 RMVar_hsa_circ_298568,RMVar_hsa_circ_327811,RMVar_hsa_circ_317185,RMVar_hsa_circ_285578,RMVar_hsa_circ_57419,RMVar_hsa_circ_64586,RMVar_hsa_circ_149872,RMVar_hsa_circ_149873,RMVar_hsa_circ_149871,RMVar_hsa_circ_316529,RMVar_hsa_circ_359549,RMVar_hsa_circ_284902,RMVar_hsa_circ_357122,RMVar_hsa_circ_149874,RMVar_hsa_circ_310274,RMVar_hsa_circ_28227,RMVar_hsa_circ_149875,RMVar_hsa_circ_149876,RMVar_hsa_circ_356358 102657 RMVar_ID_102657 Human_SNP_ID_468530863 m1A Human chr11 + 59792676 59792676 59792676 GGCAGGGCCCCGTGGAGTGGAAGGTGCTTTGGATGAGAGGAATGGTATGAACATAATCAAGAAAG GGCAGGGCCCCGTGGAGTGGAAGGTGCTTTGGGTGAGAGGAATGGTATGAACATAATCAAGAAAG A G STX3 Ensembl:ENSG00000166900 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:59792669..59792770 26863196 MeRIP-seq:(Medium) rs1455917239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11648874 RMVar_hsa_circ_298568,RMVar_hsa_circ_327811,RMVar_hsa_circ_317185,RMVar_hsa_circ_285578,RMVar_hsa_circ_57419,RMVar_hsa_circ_64586,RMVar_hsa_circ_149872,RMVar_hsa_circ_149873,RMVar_hsa_circ_149871,RMVar_hsa_circ_316529,RMVar_hsa_circ_359549,RMVar_hsa_circ_284902,RMVar_hsa_circ_357122,RMVar_hsa_circ_149874,RMVar_hsa_circ_310274,RMVar_hsa_circ_28227,RMVar_hsa_circ_149875,RMVar_hsa_circ_149876,RMVar_hsa_circ_356358 102658 RMVar_ID_102658 Human_SNP_ID_468534758 m1A Human chr11 + 59808754 59808754 59808754 GAGAAACTTACAACCTAGGAATCCTTTGATCAATGCTCTTTCTCTCATATATGCAGGGACTTTTC GAGAAACTTACAACCTAGGAATCCTTTGATCAGTGCTCTTTCTCTCATATATGCAGGGACTTTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:59808752..59808852 32194978 MeRIP-seq:(Medium) rs143463990 Functional Loss SNV dbSNP153 33..33 33 - - - 102659 RMVar_ID_102659 Human_SNP_ID_468535364 m1A Human chr11 - 59810711 59810711 59810711 AGGTAGTGGAGCGCCGCTGCTTACCTGGGTGCAGGAGACAGCCGGAGTCGCTGGGGGAGCTCCGC AGGTAGTGGAGCGCCGCTGCTTACCTGGGTGCGGGAGACAGCCGGAGTCGCTGGGGGAGCTCCGC T C MRPL16 Ensembl:ENSG00000166902 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1286659610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184877,Human_RBP_ID_22432920,Human_RBP_ID_22895031,Human_RBP_ID_26803481 102660 RMVar_ID_102660 Human_SNP_ID_78032562 m1A Human chr2 - 75060850 75060850 75060850 CCAGCTCTTCCCCCAAGCCACAGTGCTTCCTGAATCTCTCCCCTCATATCATCCATCCATCCTGC CCAGCTCTTCCCCCAAGCCACAGTGCTTCCTGTATCTCTCCCCTCATATCATCCATCCATCCTGC T A TACR1 Ensembl:ENSG00000115353 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:75060816..75060946 26863196 MeRIP-seq:(Medium) rs1052790951 Functional Loss SNV dbSNP153 33..33 33 - - - 102661 RMVar_ID_102661 Human_SNP_ID_78032666 m1A Human chr2 + 75061276 75061276 75061276 AGCCTGCCTCTGAGGGGAGGGAGGATGAGGGTAGGAACTTGCTCTCTGCTTTGGACATCAGAGAC AGCCTGCCTCTGAGGGGAGGGAGGATGAGGGTTGGAACTTGCTCTCTGCTTTGGACATCAGAGAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:75061246..75061396 26863196 MeRIP-seq:(Medium) rs993313017 Functional Loss SNV dbSNP153 33..33 33 - - - 102662 RMVar_ID_102662 Human_SNP_ID_78148330 m1A Human chr2 - 75524343 75524343 75524343 AATCTAGGATGACAGTGATAAACTGAGTGAGCAGGGAGGGGATGAGAAGATAGAAGCCTCAGAGA AATCTAGGATGACAGTGATAAACTGAGTGAGCGGGGAGGGGATGAGAAGATAGAAGCCTCAGAGA T C EVA1A Ensembl:ENSG00000115363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:75524340..75524493 26863196 MeRIP-seq:(Medium) rs936039091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312466,RMVar_hsa_circ_111939,RMVar_hsa_circ_201405,RMVar_hsa_circ_201406,RMVar_hsa_circ_347315 102663 RMVar_ID_102663 Human_SNP_ID_78193742 m1A Human chr2 + 75710493 75710493 75710493 CTGGATAAGACTCAGCATGGCTTGTGGTCGGCAGCAAGTTATAGAACCCCCAGAGAAGGATCCAG CTGGATAAGACTCAGCATGGCTTGTGGTCGGCGGCAAGTTATAGAACCCCCAGAGAAGGATCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:75710491..75710939 26863196 MeRIP-seq:(Medium) rs1421159946 Functional Loss SNV dbSNP153 33..33 33 - - - 102664 RMVar_ID_102664 Human_SNP_ID_78193978 m1A Human chr2 + 75710854 75710854 75710854 GCTGCCGAAAAGTCCTTTTCGGCCTGTGAGCCATGGCCGAGGCCCGAGCGCCCGGCGCCCTAGAA GCTGCCGAAAAGTCCTTTTCGGCCTGTGAGCCGTGGCCGAGGCCCGAGCGCCCGGCGCCCTAGAA A G AC005034.7 Ensembl:ENSG00000286045 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:75710558..75710964 26863196 MeRIP-seq:(Medium) rs1373581948 Functional Loss SNV dbSNP153 33..33 33 - - - 102665 RMVar_ID_102665 Human_SNP_ID_78193979 m1A Human chr2 + 75710854 75710854 75710854 GCTGCCGAAAAGTCCTTTTCGGCCTGTGAGCCATGGCCGAGGCCCGAGCGCCCGGCGCCCTAGAA GCTGCCGAAAAGTCCTTTTCGGCCTGTGAGCCTTGGCCGAGGCCCGAGCGCCCGGCGCCCTAGAA A T AC005034.7 Ensembl:ENSG00000286045 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:75710558..75710964 26863196 MeRIP-seq:(Medium) rs1373581948 Functional Loss SNV dbSNP153 33..33 33 - - - 102666 RMVar_ID_102666 Human_SNP_ID_78937039 m1A Human chr2 - 78379016 78379016 78379016 ATGATCTCGGCTCACCGCAACCTCCACCTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCA ATGATCTCGGCTCACCGCAACCTCCACCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCA T C LOC101927967 RNACentral:URS00008BBCD9 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:78378998..78379083 26863410 MeRIP-seq:(Medium) rs1439198988 Functional Loss SNV dbSNP153 33..33 33 - - - 102667 RMVar_ID_102667 Human_SNP_ID_80464007 m1A Human chr2 + 84425502 84425499 84425502 CTCTGAAGGGCAGAGATCTTCTCTTTAGCTCCACCTTTTCCTCCAGCAATAATTGCCCCGGCATG CTCTGAAGGGCAGAGATCTTCTCTTTAGCT___CCTTTTCCTCCAGCAATAATTGCCCCGGCATG TCCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:84425453..84425555 26863196 MeRIP-seq:(Medium) rs1375152243 Functional Loss DEL dbSNP153 31..33 33 - - - 102668 RMVar_ID_102668 Human_SNP_ID_80464604 m1A Human chr2 - 84428073 84428073 84428073 AGCATTCTGGGGTTACTGGAAGATAAGGAGAAAGGGAGGAAAGGTGGCAGATGAGGCAGGAGTAA AGCATTCTGGGGTTACTGGAAGATAAGGAGAAGGGGAGGAAAGGTGGCAGATGAGGCAGGAGTAA T C SUCLG1 Ensembl:ENSG00000163541 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:84428069..84428158 26863196 MeRIP-seq:(Medium) rs1183838735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79116,RMVar_hsa_circ_110153,RMVar_hsa_circ_115801,RMVar_hsa_circ_20573,RMVar_hsa_circ_201482,RMVar_hsa_circ_201483,RMVar_hsa_circ_201481,RMVar_hsa_circ_346539,RMVar_hsa_circ_359222,RMVar_hsa_circ_91999,RMVar_hsa_circ_201484 102669 RMVar_ID_102669 Human_SNP_ID_80555007 m1A Human chr2 - 84822871 84822871 84822871 GAAGTGAAGGAGTAATGGGGTGAGATGTGTCCAGAGAGGTAAACACGGAGGGAAGTAGGGAGCCA GAAGTGAAGGAGTAATGGGGTGAGATGTGTCCGGAGAGGTAAACACGGAGGGAAGTAGGGAGCCA T C TRABD2A Ensembl:ENSG00000186854 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:84822820..84823050 26863196 MeRIP-seq:(Medium) rs866848633 Functional Loss SNV dbSNP153 33..33 33 - - - 102670 RMVar_ID_102670 Human_SNP_ID_80556738 m1A Human chr2 + 84829851 84829849 84829851 GTACCAAACAACACACATACCAGACATGCACCACACACACACCATACACATGCACACTACACACA GTACCAAACAACACACATACCAGACATGCAC__CACACACACCATACACATGCACACTACACACA CCA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:84829804..84830087 26863196 MeRIP-seq:(Medium) rs1334469752 Functional Loss DEL dbSNP153 32..33 33 - - - 102671 RMVar_ID_102671 Human_SNP_ID_80560084 m1A Human chr2 - 84844004 84844004 84844004 CGCCTTCCAGAGAGACTGGAGGTGCCTCTGCCAGAGAAAAGGAGGAGGTATTGAGAGAAGAGAGG CGCCTTCCAGAGAGACTGGAGGTGCCTCTGCCGGAGAAAAGGAGGAGGTATTGAGAGAAGAGAGG T C TRABD2A Ensembl:ENSG00000186854 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:84844002..84844098 26863196 MeRIP-seq:(Medium) rs555720667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322510 102672 RMVar_ID_102672 Human_SNP_ID_80568998 m1A Human chr2 - 84880951 84880951 84880951 AGCTTCGCGGCGCGGGGCGCCCGGCACCGCCAACTGCGAGCTCAAGCCCCAAGTAAGGCGCGCGT AGCTTCGCGGCGCGGGGCGCCCGGCACCGCCATCTGCGAGCTCAAGCCCCAAGTAAGGCGCGCGT T A TRABD2A Ensembl:ENSG00000186854 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:84880926..84881075 26863196 MeRIP-seq:(Medium) rs1428637225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_267789,Human_Splice_Rec_267805,Human_Splice_Rec_267831 102673 RMVar_ID_102673 Human_SNP_ID_80569042 m1A Human chr2 - 84881055 84881055 84881055 CCTACTCCTTCCCTCCGCGTTCCGGGCCTCGGAGCCGCCTTGAGGAGGATGAGTCCCTGGAGCTG CCTACTCCTTCCCTCCGCGTTCCGGGCCTCGGGGCCGCCTTGAGGAGGATGAGTCCCTGGAGCTG T C TRABD2A Ensembl:ENSG00000186854 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:84881005..84881309;chr2:84881005..84881152 26863196 MeRIP-seq:(Medium) rs778273889 Functional Loss SNV dbSNP153 33..33 33 - - - 102674 RMVar_ID_102674 Human_SNP_ID_80576062 m1A Human chr2 + 84905716 84905716 84905716 GCACCAGGATCTCGGGCTCGGAACGAGACTGCACGGTGAGTGCGGCGCCGGGGCGGGGGGCCCAC GCACCAGGATCTCGGGCTCGGAACGAGACTGCTCGGTGAGTGCGGCGCCGGGGCGGGGGGCCCAC A T TMSB10 Ensembl:ENSG00000034510 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:84905651..84905819;chr2:84905651..84905788 26863196 MeRIP-seq:(Medium) rs1445228568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1590813,Human_RBP_ID_4623447,Human_RBP_ID_5471420,Human_RBP_ID_19100822,Human_RBP_ID_26485343 Human_Splice_Rec_267849 RMVar_hsa_circ_97719,RMVar_hsa_circ_201503 102675 RMVar_ID_102675 Human_SNP_ID_80578926 m1A Human chr2 + 84916082 84916082 84916082 GGAATCTGAGATCATTGATTTCTTCCTGGGGGACTCTCTCAAGGATGAGGTTTTGAAGATTATGC GGAATCTGAGATCATTGATTTCTTCCTGGGGGCCTCTCTCAAGGATGAGGTTTTGAAGATTATGC A C AC022210.1 Ensembl:ENSG00000213399 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1400191790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18515921 Human_miRNA_ID_1861537,Human_miRNA_ID_1863339,Human_miRNA_ID_1884052 102676 RMVar_ID_102676 Human_SNP_ID_80592302 m1A Human chr2 - 84970394 84970394 84970394 GAGGCCGATTCCTTGCGAACCATCTCCGTTAAAGACTCCGCGCCGGGCAGCCCGGGAGTCCGGCG GAGGCCGATTCCTTGCGAACCATCTCCGTTAAGGACTCCGCGCCGGGCAGCCCGGGAGTCCGGCG T C lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5,lnc-TRABD2A-5:6,lnc-TRABD2A-5:7,lnc-TRABD2A-5:8 RNACentral:URS0000D57E27,RNACentral:URS0000D5AC3F,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D5D245,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:84970343..84970443 26863196 MeRIP-seq:(Medium) rs1371735995 Functional Loss SNV dbSNP153 33..33 33 - - - 102677 RMVar_ID_102677 Human_SNP_ID_80592515 m1A Human chr2 - 84970982 84970981 84970982 CAGCCCCGCCTCTCGCTGCCCTCGCCGGGCCCAGCCGCCCGGAGGCCCCGCGGCCGGCGGTCGCG CAGCCCCGCCTCTCGCTGCCCTCGCCGGGCCC_GCCGCCCGGAGGCCCCGCGGCCGGCGGTCGCG CT C lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5 RNACentral:URS0000D57E27,RNACentral:URS0000D591F9,RNACentral:URS0000D5D245,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:84970937..84971036 26863196 MeRIP-seq:(Medium) rs1559121778 Functional Loss DEL dbSNP153 33..33 33 - - - 102678 RMVar_ID_102678 Human_SNP_ID_80592733 m1A Human chr2 - 84971441 84971441 84971441 TCTCACCTTCATGTCGGGACATCCTAGTTCAGACGGTGGCGGCGCGGCCCCTCCCGGGCTCCGGC TCTCACCTTCATGTCGGGACATCCTAGTTCAGGCGGTGGCGGCGCGGCCCCTCCCGGGCTCCGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:84971391..84971987 32194978 MeRIP-seq:(Medium) rs774624300 Functional Loss SNV dbSNP153 33..33 33 - - - 102679 RMVar_ID_102679 Human_SNP_ID_80592972 m1A Human chr2 + 84972117 84972117 84972117 GCTCGGGTAACCAAGTTCCCGGGGTGGATCCGACCCCGCCGCAGCAAGCAAACTCCCTGCTCAGT GCTCGGGTAACCAAGTTCCCGGGGTGGATCCGCCCCCGCCGCAGCAAGCAAACTCCCTGCTCAGT A C KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:84972113..84972236 26863196 MeRIP-seq:(Medium) rs1046515893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638773,Human_RBP_ID_5239839,Human_RBP_ID_5322109 102680 RMVar_ID_102680 Human_SNP_ID_80595271 m1A Human chr2 + 84980192 84980192 84980192 GATTTATGTTAAAGATCTGGGATAAGGCAGACAGTTTCCTAAAGGAACATATTACCTAGATTACA GATTTATGTTAAAGATCTGGGATAAGGCAGACGGTTTCCTAAAGGAACATATTACCTAGATTACA A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:84980186..84980372 26863196 MeRIP-seq:(Medium) rs1372281133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6953487,Human_RBP_ID_13970737 102681 RMVar_ID_102681 Human_SNP_ID_80633883 m1A Human chr2 + 85133464 85133464 85133464 GCGGAGCAGGCGGCGGCGGTGGCGAGTTGGGGAGCCCTAGGCTCGGCGCTGCCGGAGGGGCCCGA GCGGAGCAGGCGGCGGCGGTGGCGAGTTGGGGCGCCCTAGGCTCGGCGCTGCCGGAGGGGCCCGA A C TCF7L1 Ensembl:ENSG00000152284 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85133417..85133909 26863196 MeRIP-seq:(Medium) rs972267975 Functional Loss SNV dbSNP153 33..33 33 - - - 102682 RMVar_ID_102682 Human_SNP_ID_80634008 m1A Human chr2 - 85133745 85133722 85133746 GTCGTCCCCTCCGCCGGCCGCCCCGGCGCTGGAGCCGCCGCCTCCCCCGCTGCCGCCGCCGCCGC GTCGTCCCCTCCGCCGGCCGCCCCGGCGCTG________________________CCGCCGCCGC GCGGCAGCGGGGGAGGCGGCGGCTC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:85133413..85133889;chr2:85133707..85133889 26863196 MeRIP-seq:(Medium) rs1331869004 Functional Loss DEL dbSNP153 32..55 33 - - - 102683 RMVar_ID_102683 Human_SNP_ID_80634354 m1A Human chr2 + 85134395 85134395 85134395 GTACCCTGGGTACCCCTTCCTGATGATCCCGGACCTGAGCAGCCCGTACCTCTCCAACGGACCCC GTACCCTGGGTACCCCTTCCTGATGATCCCGGGCCTGAGCAGCCCGTACCTCTCCAACGGACCCC A G TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:85133855..85134429 32194978 MeRIP-seq:(Medium) rs756353426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4617928 Human_Splice_Rec_267896,Human_Splice_Rec_267897,Human_Splice_Rec_267915 102684 RMVar_ID_102684 Human_SNP_ID_80634359 m1A Human chr2 + 85134423 85134410 85134424 CCGGACCTGAGCAGCCCGTACCTCTCCAACGGACCCCTGTCTCCCGGAGGAGCGCGCACCGTGAG CCGGACCTGAGCAGCCCGTA______________CCCTGTCTCCCGGAGGAGCGCGCACCGTGAG ACCTCTCCAACGGAC A TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85134036..85166948 26863196 MeRIP-seq:(Medium) rs1173256832 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_556461 Human_Splice_Rec_267897,Human_Splice_Rec_267915 102685 RMVar_ID_102685 Human_SNP_ID_80635893 m1A Human chr2 + 85140904 85140904 85140904 AGAATCCAGCCTGGGCAATAAGAGCGAAAGAGAGAGAGAGACAGAAGAGAGAAAGAAAAGAGAGT AGAATCCAGCCTGGGCAATAAGAGCGAAAGAGGGAGAGAGACAGAAGAGAGAAAGAAAAGAGAGT A G TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85140900..85141087 26863196 MeRIP-seq:(Medium) rs561886975 Functional Loss SNV dbSNP153 33..33 33 - - - 102686 RMVar_ID_102686 Human_SNP_ID_80660138 m1A Human chr2 + 85244062 85244062 85244062 GGCCTCACAGGGAGGTGACAAACTCTATAGACACATACACGGGGGAAGAGCACGCCAGGCAGAGG GGCCTCACAGGGAGGTGACAAACTCTATAGACCCATACACGGGGGAAGAGCACGCCAGGCAGAGG A C TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85244057..85244172 26863196 MeRIP-seq:(Medium) rs891824152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352758 102687 RMVar_ID_102687 Human_SNP_ID_80660139 m1A Human chr2 + 85244062 85244062 85244062 GGCCTCACAGGGAGGTGACAAACTCTATAGACACATACACGGGGGAAGAGCACGCCAGGCAGAGG GGCCTCACAGGGAGGTGACAAACTCTATAGACGCATACACGGGGGAAGAGCACGCCAGGCAGAGG A G TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85244057..85244172 26863196 MeRIP-seq:(Medium) rs891824152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352758 102688 RMVar_ID_102688 Human_SNP_ID_80660285 m1A Human chr2 + 85244689 85244688 85244689 GGACATCCAGTGGGGAGAGTGATAGGTGGGGTAATTGGGTCTAGAAGTCAGGGATGAGGTCTAGG GGACATCCAGTGGGGAGAGTGATAGGTGGGGT_ATTGGGTCTAGAAGTCAGGGATGAGGTCTAGG TA T TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85244685..85244768 26863196 MeRIP-seq:(Medium) rs1429577045 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_352758 102689 RMVar_ID_102689 Human_SNP_ID_80660286 m1A Human chr2 + 85244689 85244689 85244689 GGACATCCAGTGGGGAGAGTGATAGGTGGGGTAATTGGGTCTAGAAGTCAGGGATGAGGTCTAGG GGACATCCAGTGGGGAGAGTGATAGGTGGGGTTATTGGGTCTAGAAGTCAGGGATGAGGTCTAGG A T TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85244685..85244768 26863196 MeRIP-seq:(Medium) rs1013868028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352758 102690 RMVar_ID_102690 Human_SNP_ID_80664702 m1A Human chr2 + 85263346 85263346 85263346 GGTGGAGGGGGGGAAGTAATGCAATCACAGGAAGGGTGGGCTGGCCTGGGGAGGGGCTGCCGGCA GGTGGAGGGGGGGAAGTAATGCAATCACAGGAGGGGTGGGCTGGCCTGGGGAGGGGCTGCCGGCA A G TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85263341..85263441 26863196 MeRIP-seq:(Medium) rs1358957354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352758 102691 RMVar_ID_102691 Human_SNP_ID_80674886 m1A Human chr2 + 85304190 85304190 85304190 CTTCCTTCCCATATTTCTCATCCCTTCTTCCCAAGTGCCTCTCTTCCTCTGCCCTGAGCTTTCCC CTTCCTTCCCATATTTCTCATCCCTTCTTCCCGAGTGCCTCTCTTCCTCTGCCCTGAGCTTTCCC A G TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85304186..85304275 26863196 MeRIP-seq:(Medium) rs754850306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8045 102692 RMVar_ID_102692 Human_SNP_ID_80675207 m1A Human chr2 + 85305334 85305334 85305334 CCACCCTGGCCTGCCCACCTCAGGGATCCCCCACCCTGCCATCGTCTCCCCCATCGTCAAGCAGG CCACCCTGGCCTGCCCACCTCAGGGATCCCCCCCCCTGCCATCGTCTCCCCCATCGTCAAGCAGG A C TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85303862..85305393 26863196 MeRIP-seq:(Medium) rs746637737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_267906,Human_Splice_Rec_267907 RMVar_hsa_circ_9915,RMVar_hsa_circ_8045 102693 RMVar_ID_102693 Human_SNP_ID_80676518 m1A Human chr2 + 85309296 85309296 85309296 GTCGGCTAAGGCTGCAGCCTCCTCCTCTGGGCAGATGGGCAGCCAGCCTCCCCTCCTGTCCCGGC GTCGGCTAAGGCTGCAGCCTCCTCCTCTGGGCGGATGGGCAGCCAGCCTCCCCTCCTGTCCCGGC A G TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85309247..85309455 26863196 MeRIP-seq:(Medium) rs767827910 Functional Loss SNV dbSNP153 33..33 33 - - - 102694 RMVar_ID_102694 Human_SNP_ID_80676519 m1A Human chr2 + 85309298 85309298 85309298 CGGCTAAGGCTGCAGCCTCCTCCTCTGGGCAGATGGGCAGCCAGCCTCCCCTCCTGTCCCGGCCC CGGCTAAGGCTGCAGCCTCCTCCTCTGGGCAGCTGGGCAGCCAGCCTCCCCTCCTGTCCCGGCCC A C TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85309247..85309545 26863196 MeRIP-seq:(Medium) rs1300843452 Functional Loss SNV dbSNP153 33..33 33 - - - 102695 RMVar_ID_102695 Human_SNP_ID_80676679 m1A Human chr2 - 85309790 85309790 85309790 AGCTGGGGCAGGCGGCAGGGGCGAGAAGAGACAGGAGACAGAAAGTGCAAGAGAGGTAAGAGAGA AGCTGGGGCAGGCGGCAGGGGCGAGAAGAGACGGGAGACAGAAAGTGCAAGAGAGGTAAGAGAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85309741..85309904 26863196 MeRIP-seq:(Medium) rs777434861 Functional Loss SNV dbSNP153 33..33 33 - - - 102696 RMVar_ID_102696 Human_SNP_ID_80676680 m1A Human chr2 - 85309790 85309790 85309790 AGCTGGGGCAGGCGGCAGGGGCGAGAAGAGACAGGAGACAGAAAGTGCAAGAGAGGTAAGAGAGA AGCTGGGGCAGGCGGCAGGGGCGAGAAGAGACCGGAGACAGAAAGTGCAAGAGAGGTAAGAGAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85309741..85309904 26863196 MeRIP-seq:(Medium) rs777434861 Functional Loss SNV dbSNP153 33..33 33 - - - 102697 RMVar_ID_102697 Human_SNP_ID_80676694 m1A Human chr2 + 85309829 85309829 85309829 TCTCGCCCCTGCCGCCTGCCCCAGCTTCCCCGACTCCATCTGCAGCTCTGCCATTGTGACATTTC TCTCGCCCCTGCCGCCTGCCCCAGCTTCCCCGGCTCCATCTGCAGCTCTGCCATTGTGACATTTC A G TCF7L1 Ensembl:ENSG00000152284 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85309790..85310031 26863196 MeRIP-seq:(Medium) rs757965981 Functional Loss SNV dbSNP153 33..33 33 - - - 102698 RMVar_ID_102698 Human_SNP_ID_80676700 m1A Human chr2 - 85309858 85309858 85309858 AGACGATGAAAACTTGGGCTGGGTAACAGGAAATGTCACAATGGCAGAGCTGCAGATGGAGTCGG AGACGATGAAAACTTGGGCTGGGTAACAGGAAGTGTCACAATGGCAGAGCTGCAGATGGAGTCGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85309809..85309925 26863196 MeRIP-seq:(Medium) rs935149453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13972047 102699 RMVar_ID_102699 Human_SNP_ID_80681000 m1A Human chr2 - 85327052 85327052 85327052 TCCAAAAGACGGCTCTAACAAGTCCGGTGCAGAGGAGCAGGGCCCAATAGACGGGCCCAGCAAGT TCCAAAAGACGGCTCTAACAAGTCCGGTGCAGCGGAGCAGGGCCCAATAGACGGGCCCAGCAAGT T G TGOLN2 Ensembl:ENSG00000152291 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85327001..85327150 32194978 MeRIP-seq:(Medium) rs1021451242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9384115,Human_RBP_ID_22765448,Human_RBP_ID_26339495,Human_RBP_ID_27817276 Human_Splice_Rec_267945 Human_miRNA_ID_2380030,Human_miRNA_ID_3023044 RMVar_hsa_circ_201519,RMVar_hsa_circ_53992,RMVar_hsa_circ_265020,RMVar_hsa_circ_376908 102700 RMVar_ID_102700 Human_SNP_ID_80681114 m1A Human chr2 - 85327258 85327258 85327258 GAAGACAGCCCCAACAGGTCGGGTGCGGAGGCAAAGACCCAAAAAGACAGCCCTAGCAAGTCAGG GAAGACAGCCCCAACAGGTCGGGTGCGGAGGCGAAGACCCAAAAAGACAGCCCTAGCAAGTCAGG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:85327056..85327500 26863196 MeRIP-seq:(Medium) rs1172966668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778269,Human_RBP_ID_22450421,Human_RBP_ID_22765874,Human_RBP_ID_26341046 RMVar_hsa_circ_53992 102701 RMVar_ID_102701 Human_SNP_ID_80681118 m1A Human chr2 + 85327267 85327267 85327267 CTAGGGCTGTCTTTTTGGGTCTTTGCCTCCGCACCCGACCTGTTGGGGCTGTCTTCTGGGGTCTG CTAGGGCTGTCTTTTTGGGTCTTTGCCTCCGCTCCCGACCTGTTGGGGCTGTCTTCTGGGGTCTG A T L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:85327187..85327500 26863196 MeRIP-seq:(Medium) rs780168951 Functional Loss SNV dbSNP153 33..33 33 - - - 102702 RMVar_ID_102702 Human_SNP_ID_80686583 m1A Human chr2 - 85345969 85345968 85345969 TGCCGGGGAACGCCCGCTGCCTGCCAGGTAAAAGGCGGGTCTGCACTGCCCCTCTTGCAGGTTCC TGCCGGGGAACGCCCGCTGCCTGCCAGGTAAA_GGCGGGTCTGCACTGCCCCTCTTGCAGGTTCC CT C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85345965..85346065 32194978 MeRIP-seq:(Medium) rs751613807 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_19002020,Human_RBP_ID_19097774 102703 RMVar_ID_102703 Human_SNP_ID_80687688 m1A Human chr2 + 85350145 85350145 85350145 CAGGCTCTGGGTGGATGCTTGAAGGAATGGAGAGAAACGAGTCAGCAGCCCACACCTGTCGAGGA CAGGCTCTGGGTGGATGCTTGAAGGAATGGAGGGAAACGAGTCAGCAGCCCACACCTGTCGAGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85350094..85350194 32194978 MeRIP-seq:(Medium) rs778715256 Functional Loss SNV dbSNP153 33..33 33 - - - 102704 RMVar_ID_102704 Human_SNP_ID_80688166 m1A Human chr2 - 85351864 85351864 85351864 CTGAGAAACCCACCCTTTGGCCCTTCTGCTGTAGCTTTTTCAGCCAACCAAGTGCCGGAGAAGCT CTGAGAAACCCACCCTTTGGCCCTTCTGCTGTGGCTTTTTCAGCCAACCAAGTGCCGGAGAAGCT T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85351849..85354472 32194978 MeRIP-seq:(Medium) rs147080219 Functional Loss SNV dbSNP153 33..33 33 - - - 102705 RMVar_ID_102705 Human_SNP_ID_80688760 m1A Human chr2 + 85354485 85354485 85354485 TGCAGAGGACGGCCAGCAGCAGCACAGCCAGGAGCAGCACCAGCGGAAGCCACATCACGCCGGCG TGCAGAGGACGGCCAGCAGCAGCACAGCCAGGGGCAGCACCAGCGGAAGCCACATCACGCCGGCG A G ELMOD3 Ensembl:ENSG00000115459 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85354372..85354593 26863196 MeRIP-seq:(Medium) rs1403167106 Functional Loss SNV dbSNP153 33..33 33 - - - 102706 RMVar_ID_102706 Human_SNP_ID_80688761 m1A Human chr2 + 85354485 85354485 85354485 TGCAGAGGACGGCCAGCAGCAGCACAGCCAGGAGCAGCACCAGCGGAAGCCACATCACGCCGGCG TGCAGAGGACGGCCAGCAGCAGCACAGCCAGGTGCAGCACCAGCGGAAGCCACATCACGCCGGCG A T ELMOD3 Ensembl:ENSG00000115459 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85354372..85354593 26863196 MeRIP-seq:(Medium) rs1403167106 Functional Loss SNV dbSNP153 33..33 33 - - - 102707 RMVar_ID_102707 Human_SNP_ID_80688913 m1A Human chr2 + 85354826 85354826 85354826 CGGCGGGACCCCCAAGTTTGGAAAGCTCTTTTAACGGTGAGAACGCGTTAACACTTGCCAAGGGG CGGCGGGACCCCCAAGTTTGGAAAGCTCTTTTTACGGTGAGAACGCGTTAACACTTGCCAAGGGG A T ELMOD3 Ensembl:ENSG00000115459 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85354785..85354907 26863196 MeRIP-seq:(Medium) rs562214129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421835,Human_RBP_ID_19097780 Human_Splice_Rec_268035,Human_Splice_Rec_268039,Human_Splice_Rec_268055,Human_Splice_Rec_268077,Human_Splice_Rec_268097,Human_Splice_Rec_268117,Human_Splice_Rec_268145,Human_Splice_Rec_268169,Human_Splice_Rec_268177,Human_Splice_Rec_268189,Human_Splice_Rec_268215,Human_Splice_Rec_268221,Human_Splice_Rec_268241 102708 RMVar_ID_102708 Human_SNP_ID_80689726 m1A Human chr2 + 85358456 85358456 85358456 TGCCTTGAGTAGGTGGAACTGACCTTGATCAGAGAAGAGAGTGGAGGTGTATTCTGGAGGAAAAC TGCCTTGAGTAGGTGGAACTGACCTTGATCAGGGAAGAGAGTGGAGGTGTATTCTGGAGGAAAAC A G ELMOD3 Ensembl:ENSG00000115459 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85358405..85358529 26863196 MeRIP-seq:(Medium) rs1417396024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292436,RMVar_hsa_circ_87682,RMVar_hsa_circ_353948,RMVar_hsa_circ_201526,RMVar_hsa_circ_313740,RMVar_hsa_circ_14642,RMVar_hsa_circ_201528 102709 RMVar_ID_102709 Human_SNP_ID_80698370 m1A Human chr2 - 85394893 85394893 85394893 ATCTTCAAGCAATTTTTCAAGGACTGGAAATGAGGGTGGGCGTCTTCCTGCCCCATGCTCCCCTG ATCTTCAAGCAATTTTTCAAGGACTGGAAATGCGGGTGGGCGTCTTCCTGCCCCATGCTCCCCTG T G CAPG Ensembl:ENSG00000042493 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85394843..85394915 26863196 MeRIP-seq:(Medium) rs759747470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17658523,Human_RBP_ID_22449893 Human_Splice_Rec_268374,Human_Splice_Rec_268392,Human_Splice_Rec_268410,Human_Splice_Rec_268428,Human_Splice_Rec_268444,Human_Splice_Rec_268448 Human_miRNA_ID_3056772 RMVar_hsa_circ_76432,RMVar_hsa_circ_116449,RMVar_hsa_circ_128194,RMVar_hsa_circ_93221,RMVar_hsa_circ_201541,RMVar_hsa_circ_201543,RMVar_hsa_circ_201544,RMVar_hsa_circ_201542 102710 RMVar_ID_102710 Human_SNP_ID_80699395 m1A Human chr2 - 85398770 85398770 85398770 GCCTGCCCTGGCCCCTGCAGGTCCTGGGCCCCAAGCCTGCTCTGAAGGAGGGCAACCCTGAGGAA GCCTGCCCTGGCCCCTGCAGGTCCTGGGCCCCCAGCCTGCTCTGAAGGAGGGCAACCCTGAGGAA T G CAPG Ensembl:ENSG00000042493 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:85398726..85398800 32194978 MeRIP-seq:(Medium) rs1454358596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8851973,Human_RBP_ID_17964072,Human_RBP_ID_22449895 Human_Splice_Rec_268369,Human_Splice_Rec_268386,Human_Splice_Rec_268387,Human_Splice_Rec_268404,Human_Splice_Rec_268405,Human_Splice_Rec_268422,Human_Splice_Rec_268423,Human_Splice_Rec_268438,Human_Splice_Rec_268439,Human_Splice_Rec_268454,Human_Splice_Rec_268455,Human_Splice_Rec_268472,Human_Splice_Rec_268484,Human_Splice_Rec_268496,Human_Splice_Rec_268506 Human_miRNA_ID_2250923 RMVar_hsa_circ_76432,RMVar_hsa_circ_116449,RMVar_hsa_circ_93221,RMVar_hsa_circ_201543,RMVar_hsa_circ_201544,RMVar_hsa_circ_201542,RMVar_hsa_circ_201546,RMVar_hsa_circ_99544,RMVar_hsa_circ_287995,RMVar_hsa_circ_201545 102711 RMVar_ID_102711 Human_SNP_ID_80699553 m1A Human chr2 + 85399224 85399224 85399224 CCTGTCGCTCACTGTCCCGGATGGCCAGGGCCAGGTCCCTCGCCTTGTTGCGTTCCAGGATGTTG CCTGTCGCTCACTGTCCCGGATGGCCAGGGCCGGGTCCCTCGCCTTGTTGCGTTCCAGGATGTTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:85399176..85399250 26863196 MeRIP-seq:(Medium) rs1437133946 Functional Loss SNV dbSNP153 33..33 33 - - - 102712 RMVar_ID_102712 Human_SNP_ID_80699559 m1A Human chr2 - 85399237 85399237 85399237 GTGGTGGAAAGTCCAACATCCTGGAACGCAACAAGGCGAGGGACCTGGCCCTGGCCATCCGGGAC GTGGTGGAAAGTCCAACATCCTGGAACGCAACGAGGCGAGGGACCTGGCCCTGGCCATCCGGGAC T C CAPG Ensembl:ENSG00000042493 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85399186..85399313 26863196 MeRIP-seq:(Medium) rs1558731402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_268384,Human_Splice_Rec_268402,Human_Splice_Rec_268403,Human_Splice_Rec_268420,Human_Splice_Rec_268436,Human_Splice_Rec_268452,Human_Splice_Rec_268470,Human_Splice_Rec_268482,Human_Splice_Rec_268494,Human_Splice_Rec_268504,Human_Splice_Rec_268516 Human_miRNA_ID_2661130,Human_miRNA_ID_2679584 RMVar_hsa_circ_76432,RMVar_hsa_circ_93221,RMVar_hsa_circ_201543,RMVar_hsa_circ_201544,RMVar_hsa_circ_201546,RMVar_hsa_circ_99544,RMVar_hsa_circ_287995,RMVar_hsa_circ_201545 102713 RMVar_ID_102713 Human_SNP_ID_80699570 m1A Human chr2 - 85399262 85399262 85399262 TCCTTGCAGAACATCTTCGCCTGGTGTGGTGGAAAGTCCAACATCCTGGAACGCAACAAGGCGAG TCCTTGCAGAACATCTTCGCCTGGTGTGGTGGCAAGTCCAACATCCTGGAACGCAACAAGGCGAG T G CAPG Ensembl:ENSG00000042493 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:85399251..85399275 26863196 MeRIP-seq:(Medium) rs753037997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_268384,Human_Splice_Rec_268402,Human_Splice_Rec_268403,Human_Splice_Rec_268420,Human_Splice_Rec_268436,Human_Splice_Rec_268452,Human_Splice_Rec_268470,Human_Splice_Rec_268482,Human_Splice_Rec_268494,Human_Splice_Rec_268504,Human_Splice_Rec_268516 RMVar_hsa_circ_76432,RMVar_hsa_circ_93221,RMVar_hsa_circ_201543,RMVar_hsa_circ_201544,RMVar_hsa_circ_201546,RMVar_hsa_circ_99544,RMVar_hsa_circ_287995,RMVar_hsa_circ_201545 102714 RMVar_ID_102714 Human_SNP_ID_80700092 m1A Human chr2 - 85401239 85401239 85401239 AGAAACTCTACCAGGTGAAGGGGAAGAAGAACATCCGTGCCACCGAGCGGGCACTGAACTGGGAC AGAAACTCTACCAGGTGAAGGGGAAGAAGAACCTCCGTGCCACCGAGCGGGCACTGAACTGGGAC T G CAPG Ensembl:ENSG00000042493 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85401146..85401272 26863196 MeRIP-seq:(Medium) rs1381355749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9331073 Human_Splice_Rec_268382,Human_Splice_Rec_268383,Human_Splice_Rec_268400,Human_Splice_Rec_268401,Human_Splice_Rec_268418,Human_Splice_Rec_268419,Human_Splice_Rec_268434,Human_Splice_Rec_268435,Human_Splice_Rec_268450,Human_Splice_Rec_268451,Human_Splice_Rec_268468,Human_Splice_Rec_268469,Human_Splice_Rec_268480,Human_Splice_Rec_268481,Human_Splice_Rec_268492,Human_Splice_Rec_268493,Human_Splice_Rec_268502,Human_Splice_Rec_268503,Human_Splice_Rec_268514,Human_Splice_Rec_268515,Human_Splice_Rec_268526 Human_miRNA_ID_2589908 RMVar_hsa_circ_76432,RMVar_hsa_circ_93221,RMVar_hsa_circ_16168,RMVar_hsa_circ_201543,RMVar_hsa_circ_201544,RMVar_hsa_circ_99544,RMVar_hsa_circ_201545 102715 RMVar_ID_102715 Human_SNP_ID_80700368 m1A Human chr2 + 85401895 85401895 85401895 CCTGGTTCTCTTGCGCCACAGGCACCGGCTTCAGCTTCTCCACCCGCCACACATGCAGGCCTGGA CCTGGTTCTCTTGCGCCACAGGCACCGGCTTCCGCTTCTCCACCCGCCACACATGCAGGCCTGGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85401844..85401950 26863196 MeRIP-seq:(Medium) rs776366363 Functional Loss SNV dbSNP153 33..33 33 - - - 102716 RMVar_ID_102716 Human_SNP_ID_80700459 m1A Human chr2 - 85402160 85402160 85402160 TTTGTAATAATAATGGCTTCTTCTTTCTTTCCAGATCTGAAGACAGCATGTACACAGCCATTCCC TTTGTAATAATAATGGCTTCTTCTTTCTTTCCCGATCTGAAGACAGCATGTACACAGCCATTCCC T G CAPG Ensembl:ENSG00000042493 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85402101..85402175 26863196 MeRIP-seq:(Medium) rs778985139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623457 Human_Splice_Rec_268377,Human_Splice_Rec_268395,Human_Splice_Rec_268413,Human_Splice_Rec_268429,Human_Splice_Rec_268463,Human_Splice_Rec_268475,Human_Splice_Rec_268487,Human_Splice_Rec_268509,Human_Splice_Rec_268519 102717 RMVar_ID_102717 Human_SNP_ID_80703384 m1A Human chr2 + 85413916 85413916 85413916 AGAGGAGGGAGCGGGGCGCCCCCGAACCGGCTAAGCCCGTTCGACCCCTACATGGGGAGCCCAGG AGAGGAGGGAGCGGGGCGCCCCCGAACCGGCTTAGCCCGTTCGACCCCTACATGGGGAGCCCAGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85413912..85414025 26863196 MeRIP-seq:(Medium) rs1402480825 Functional Loss SNV dbSNP153 33..33 33 - - - 102718 RMVar_ID_102718 Human_SNP_ID_80705179 m1A Human chr2 + 85421105 85421105 85421105 GGGAGGGTAGAAGACCAGCTGGGAACAGGAGAAGCTTGGCTCCCAGGCTCTGTGCTGAAGAAGGA GGGAGGGTAGAAGACCAGCTGGGAACAGGAGACGCTTGGCTCCCAGGCTCTGTGCTGAAGAAGGA A C AC062037.4,SH2D6 Ensembl:ENSG00000286011,Ensembl:ENSG00000152292 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85421095..85421298 26863196 MeRIP-seq:(Medium) rs959340038 Functional Loss SNV dbSNP153 33..33 33 - - - 102719 RMVar_ID_102719 Human_SNP_ID_80735441 m1A Human chr2 + 85539313 85539313 85539313 CACCAACATGAACGGACAGCTCAACGGCTTCCACGAGGCGTTCATCGAGGAGGGCACATTCCTTT CACCAACATGAACGGACAGCTCAACGGCTTCCCCGAGGCGTTCATCGAGGAGGGCACATTCCTTT A C MAT2A Ensembl:ENSG00000168906 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85539264..85539400 32194978 MeRIP-seq:(Medium) rs1243754872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1590934,Human_RBP_ID_1924049,Human_RBP_ID_3635417,Human_RBP_ID_3959162,Human_RBP_ID_6953993,Human_RBP_ID_9386916,Human_RBP_ID_13972935,Human_RBP_ID_18443847,Human_RBP_ID_18766453,Human_RBP_ID_22816331,Human_RBP_ID_27015454 Human_Splice_Rec_268773,Human_Splice_Rec_268775,Human_Splice_Rec_268779 Human_miRNA_ID_3003192 RMVar_hsa_circ_91716,RMVar_hsa_circ_201547 102720 RMVar_ID_102720 Human_SNP_ID_80735444 m1A Human chr2 + 85539316 85539316 85539316 CAACATGAACGGACAGCTCAACGGCTTCCACGAGGCGTTCATCGAGGAGGGCACATTCCTTTTCA CAACATGAACGGACAGCTCAACGGCTTCCACGGGGCGTTCATCGAGGAGGGCACATTCCTTTTCA A G MAT2A Ensembl:ENSG00000168906 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:85539176..85539408 26863196 MeRIP-seq:(Medium) rs1191664862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1590936,Human_RBP_ID_1924049,Human_RBP_ID_3635417,Human_RBP_ID_3959162,Human_RBP_ID_6953993,Human_RBP_ID_9386916,Human_RBP_ID_13972935,Human_RBP_ID_18443847,Human_RBP_ID_18766453,Human_RBP_ID_22816331,Human_RBP_ID_27015454 Human_Splice_Rec_268773,Human_Splice_Rec_268775,Human_Splice_Rec_268779 RMVar_hsa_circ_91716,RMVar_hsa_circ_201547 102721 RMVar_ID_102721 Human_SNP_ID_80736622 m1A Human chr2 + 85542591 85542591 85542591 TTTCAGGGTGATGCTGGTTTGACTGGACGCAAAATCATTGTGGACACTTATGGCGGTTGGGGTGC TTTCAGGGTGATGCTGGTTTGACTGGACGCAAGATCATTGTGGACACTTATGGCGGTTGGGGTGC A G MAT2A Ensembl:ENSG00000168906 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr2:85542564..85542689;chr2:85542551..85542625 26863196 MeRIP-seq:(Medium) rs775270491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60191,Human_RBP_ID_243154,Human_RBP_ID_922829,Human_RBP_ID_1024410,Human_RBP_ID_1590982,Human_RBP_ID_1924076,Human_RBP_ID_3635431,Human_RBP_ID_3959173,Human_RBP_ID_5589635,Human_RBP_ID_8850230,Human_RBP_ID_9384134,Human_RBP_ID_13973029,Human_RBP_ID_17962459,Human_RBP_ID_18443850,Human_RBP_ID_18766489,Human_RBP_ID_22995810,Human_RBP_ID_23211638,Human_RBP_ID_25576765,Human_RBP_ID_26338616,Human_RBP_ID_27698999 Human_Splice_Rec_268790,Human_Splice_Rec_268818 RMVar_hsa_circ_11871,RMVar_hsa_circ_284591,RMVar_hsa_circ_201554,RMVar_hsa_circ_201551,RMVar_hsa_circ_89723,RMVar_hsa_circ_291758,RMVar_hsa_circ_288031,RMVar_hsa_circ_95573,RMVar_hsa_circ_201553,RMVar_hsa_circ_275808,RMVar_hsa_circ_293493,RMVar_hsa_circ_201555 102722 RMVar_ID_102722 Human_SNP_ID_80736635 m1A Human chr2 - 85542616 85542614 85542616 TCCTGAAAAGGCACCTCCTCCATGAGCACCCCAACCGCCATAAGTGTCCACAATGATTTTGCGTC TCCTGAAAAGGCACCTCCTCCATGAGCACCCC__CCGCCATAAGTGTCCACAATGATTTTGCGTC GTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85542544..85542700 26863196 MeRIP-seq:(Medium) rs1491230444 Functional Loss DEL dbSNP153 33..34 33 - - - 102723 RMVar_ID_102723 Human_SNP_ID_80736638 m1A Human chr2 - 85542616 85542616 85542616 TCCTGAAAAGGCACCTCCTCCATGAGCACCCCAACCGCCATAAGTGTCCACAATGATTTTGCGTC TCCTGAAAAGGCACCTCCTCCATGAGCACCCCCACCGCCATAAGTGTCCACAATGATTTTGCGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85542544..85542700 26863196 MeRIP-seq:(Medium) rs1186850719 Functional Loss SNV dbSNP153 33..33 33 - - - 102724 RMVar_ID_102724 Human_SNP_ID_80736799 m1A Human chr2 - 85543020 85543020 85543020 AGGCTTTACCATCTTTACCTGACAATGACCCCAGGGCGGAGATCGAAATTCTTCTTCACAATCTC AGGCTTTACCATCTTTACCTGACAATGACCCCGGGGCGGAGATCGAAATTCTTCTTCACAATCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85542972..85543180 26863196 MeRIP-seq:(Medium) rs1380348434 Functional Loss SNV dbSNP153 33..33 33 - - - 102725 RMVar_ID_102725 Human_SNP_ID_80736800 m1A Human chr2 + 85543027 85543027 85543027 TGAAGAAGAATTTCGATCTCCGCCCTGGGGTCATTGTCAGGTAAAGATGGTAAAGCCTGTTGCTA TGAAGAAGAATTTCGATCTCCGCCCTGGGGTCGTTGTCAGGTAAAGATGGTAAAGCCTGTTGCTA A G MAT2A Ensembl:ENSG00000168906 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85542976..85543125 26863196 MeRIP-seq:(Medium) rs768392038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60192,Human_RBP_ID_243156,Human_RBP_ID_306006,Human_RBP_ID_829811,Human_RBP_ID_922833,Human_RBP_ID_1924081,Human_RBP_ID_2667009,Human_RBP_ID_5381294,Human_RBP_ID_9998290,Human_RBP_ID_17616789,Human_RBP_ID_19100853,Human_RBP_ID_22595744,Human_RBP_ID_22996842,Human_RBP_ID_23115134,Human_RBP_ID_24546096,Human_RBP_ID_25592033,Human_RBP_ID_26339504 Human_Splice_Rec_268793 RMVar_hsa_circ_284591,RMVar_hsa_circ_201551,RMVar_hsa_circ_89723,RMVar_hsa_circ_291758,RMVar_hsa_circ_288031,RMVar_hsa_circ_42647,RMVar_hsa_circ_275808 102726 RMVar_ID_102726 Human_SNP_ID_80736848 m1A Human chr2 + 85543153 85543153 85543153 GAAGGAAGACTCCTCAAATGGGAATATATTTTAATTCCTGGAACAGTTTTGAACTGCTGCCTTAG GAAGGAAGACTCCTCAAATGGGAATATATTTTGATTCCTGGAACAGTTTTGAACTGCTGCCTTAG A G MAT2A Ensembl:ENSG00000168906 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85543125..85543474 32194978 MeRIP-seq:(Medium) rs1253499658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60193,Human_RBP_ID_1924084,Human_RBP_ID_2667015,Human_RBP_ID_9112786,Human_RBP_ID_9998292,Human_RBP_ID_13973055,Human_RBP_ID_17962462,Human_RBP_ID_22995821,Human_RBP_ID_27015498,Human_RBP_ID_27292906 Human_miRNA_ID_2031347,Human_miRNA_ID_2886285 RMVar_hsa_circ_201551,RMVar_hsa_circ_89723 102727 RMVar_ID_102727 Human_SNP_ID_80737088 m1A Human chr2 + 85544128 85544128 85544128 ATAATTGCATTGACTTTCCCCACCAGATGCTGAAAATGTCCTTGTGATGTGCACGTAAAGTACTT ATAATTGCATTGACTTTCCCCACCAGATGCTGGAAATGTCCTTGTGATGTGCACGTAAAGTACTT A G MAT2A Ensembl:ENSG00000168906 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85544078..85544169 26863196 MeRIP-seq:(Medium) rs1246905898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61632,Human_RBP_ID_556628,Human_RBP_ID_1302569,Human_RBP_ID_1591002,Human_RBP_ID_1924097,Human_RBP_ID_2667043,Human_RBP_ID_3635440,Human_RBP_ID_4634903,Human_RBP_ID_8526282,Human_RBP_ID_9998320,Human_RBP_ID_13973129,Human_RBP_ID_17192649,Human_RBP_ID_17509018,Human_RBP_ID_18319613,Human_RBP_ID_18766503,Human_RBP_ID_20438288,Human_RBP_ID_22816358,Human_RBP_ID_22995856,Human_RBP_ID_23887348,Human_RBP_ID_26485519 102728 RMVar_ID_102728 Human_SNP_ID_80737976 m1A Human chr2 - 85546665 85546665 85546665 AGGAACCTTGCTCTGGCCCAGGCTGGAGTGCAATGGCGCCATCTCGGCTCACTGCAACCTCTGCC AGGAACCTTGCTCTGGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAACCTCTGCC T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs563109158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23887366 102729 RMVar_ID_102729 Human_SNP_ID_80746043 m1A Human chr2 + 85577611 85577611 85577611 GAGGGCCACCCTGGGAGGAAGCCGACTAGGCGAATTCACTTACTGACCGGCCTGGGCTGCTCTGA GAGGGCCACCCTGGGAGGAAGCCGACTAGGCGGATTCACTTACTGACCGGCCTGGGCTGCTCTGA A G VAMP8 Ensembl:ENSG00000118640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85577551..85579212 26863196 MeRIP-seq:(Medium) rs554019226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1197097,Human_RBP_ID_4623460,Human_RBP_ID_23887397 Human_Splice_Rec_268919,Human_Splice_Rec_268923 RMVar_hsa_circ_91790,RMVar_hsa_circ_201564 102730 RMVar_ID_102730 Human_SNP_ID_80746044 m1A Human chr2 + 85577611 85577611 85577611 GAGGGCCACCCTGGGAGGAAGCCGACTAGGCGAATTCACTTACTGACCGGCCTGGGCTGCTCTGA GAGGGCCACCCTGGGAGGAAGCCGACTAGGCGTATTCACTTACTGACCGGCCTGGGCTGCTCTGA A T VAMP8 Ensembl:ENSG00000118640 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85577551..85579212 26863196 MeRIP-seq:(Medium) rs554019226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1197097,Human_RBP_ID_4623460,Human_RBP_ID_23887397 Human_Splice_Rec_268919,Human_Splice_Rec_268923 RMVar_hsa_circ_91790,RMVar_hsa_circ_201564 102731 RMVar_ID_102731 Human_SNP_ID_80746046 m1A Human chr2 + 85577616 85577616 85577616 CCACCCTGGGAGGAAGCCGACTAGGCGAATTCACTTACTGACCGGCCTGGGCTGCTCTGAGACAT CCACCCTGGGAGGAAGCCGACTAGGCGAATTCTCTTACTGACCGGCCTGGGCTGCTCTGAGACAT A T VAMP8 Ensembl:ENSG00000118640 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85577551..85579175 26863196 MeRIP-seq:(Medium) rs1215276015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1197097,Human_RBP_ID_4623460,Human_RBP_ID_8850240,Human_RBP_ID_23887397 Human_Splice_Rec_268919,Human_Splice_Rec_268923 RMVar_hsa_circ_91790,RMVar_hsa_circ_201564 102732 RMVar_ID_102732 Human_SNP_ID_80750693 m1A Human chr2 + 85596614 85596614 85596614 GCCTCCACCAGCTGCCAAGACTGTGGTTGAGAACCTCCCCAGGACAGTCATCAGAGGCTCTCAGG GCCTCCACCAGCTGCCAAGACTGTGGTTGAGAGCCTCCCCAGGACAGTCATCAGAGGCTCTCAGG A G RNF181 Ensembl:ENSG00000168894 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:85596501..85596625 32194978 MeRIP-seq:(Medium) rs746734785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776448,Human_RBP_ID_1924118,Human_RBP_ID_4618407,Human_RBP_ID_9112806,Human_RBP_ID_22450446,Human_RBP_ID_26818690 Human_Splice_Rec_268936,Human_Splice_Rec_268938,Human_Splice_Rec_268939,Human_Splice_Rec_268944,Human_Splice_Rec_268945,Human_Splice_Rec_268952,Human_Splice_Rec_268953,Human_Splice_Rec_268956,Human_Splice_Rec_268957,Human_Splice_Rec_268964,Human_Splice_Rec_268965 Human_miRNA_ID_843369,Human_miRNA_ID_2038639,Human_miRNA_ID_2365988,Human_miRNA_ID_3013791,Human_miRNA_ID_3017621 RMVar_hsa_circ_8601,RMVar_hsa_circ_127154,RMVar_hsa_circ_44140,RMVar_hsa_circ_201570 102733 RMVar_ID_102733 Human_SNP_ID_80750876 m1A Human chr2 + 85597140 85597140 85597140 ATTCCTGTCCCTTGTGCCGCTATGAGCTGCCCACTGATGACGACACTTATGAGGAGCACAGACGA ATTCCTGTCCCTTGTGCCGCTATGAGCTGCCCTCTGATGACGACACTTATGAGGAGCACAGACGA A T RNF181 Ensembl:ENSG00000168894 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:85597101..85597200 32194978 MeRIP-seq:(Medium) rs767217569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556673,Human_RBP_ID_1302576,Human_RBP_ID_1591028,Human_RBP_ID_17657445,Human_RBP_ID_22449901 Human_Splice_Rec_268942,Human_Splice_Rec_268948,Human_Splice_Rec_268949,Human_Splice_Rec_268960,Human_Splice_Rec_268961,Human_Splice_Rec_268967 RMVar_hsa_circ_8601 102734 RMVar_ID_102734 Human_SNP_ID_80750882 m1A Human chr2 - 85597157 85597157 85597157 TCAGCCCCTACCTTATCTCGTCTGTGCTCCTCATAAGTGTCGTCATCAGTGGGCAGCTCATAGCG TCAGCCCCTACCTTATCTCGTCTGTGCTCCTCGTAAGTGTCGTCATCAGTGGGCAGCTCATAGCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85597101..85597223 32194978 MeRIP-seq:(Medium) rs1234793025 Functional Loss SNV dbSNP153 33..33 33 - - - 102735 RMVar_ID_102735 Human_SNP_ID_80754167 m1A Human chr2 - 85609588 85609588 85609588 CCCTCTTCTTTCTTACTGTGGTTCATCCTTCCAGATGTCTCTGCCCACCCACGCAACCCAGACTA CCCTCTTCTTTCTTACTGTGGTTCATCCTTCCCGATGTCTCTGCCCACCCACGCAACCCAGACTA T G C2orf68 Ensembl:ENSG00000168887 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85609548..85610281 26863196 MeRIP-seq:(Medium) rs1367466415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13973635,Human_RBP_ID_25568318 102736 RMVar_ID_102736 Human_SNP_ID_80754994 m1A Human chr2 - 85611885 85611885 85611885 ACGGCTTCGTGCACCATATCCGACGGAACCAGATCGCTCGGTACCGCCCCGCCCTGCGCCGCCGC ACGGCTTCGTGCACCATATCCGACGGAACCAGTTCGCTCGGTACCGCCCCGCCCTGCGCCGCCGC T A C2orf68 Ensembl:ENSG00000168887 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85611565..85612075 26863196 MeRIP-seq:(Medium) rs1243107307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623463 Human_Splice_Rec_269329,Human_Splice_Rec_269343 102737 RMVar_ID_102737 Human_SNP_ID_80756383 m1A Human chr2 + 85616305 85616305 85616305 TCGCGTCAAGCGGGAGCGAGATCGGGAGCGGGAGCCTGAGGCGGCGAGCTCCCGGGGCAGCCCTG TCGCGTCAAGCGGGAGCGAGATCGGGAGCGGGTGCCTGAGGCGGCGAGCTCCCGGGGCAGCCCTG A T USP39 Ensembl:ENSG00000168883 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:85616186..85616421 26863196 MeRIP-seq:(Medium) rs371736825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243149,Human_RBP_ID_829907,Human_RBP_ID_4625473,Human_RBP_ID_5322111,Human_RBP_ID_8851975,Human_RBP_ID_22449903,Human_RBP_ID_23887435 RMVar_hsa_circ_80304,RMVar_hsa_circ_201576 102738 RMVar_ID_102738 Human_SNP_ID_80756459 m1A Human chr2 - 85616404 85616404 85616404 CCTCATCGACCTCGCGCTCCCGCTTCACCCGCACAAACGGGACAACAGAAGCCGGGGCCTCGCGC CCTCATCGACCTCGCGCTCCCGCTTCACCCGCCCAAACGGGACAACAGAAGCCGGGGCCTCGCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:85616226..85621217 26863410 MeRIP-seq:(Medium) rs1204521116 Functional Loss SNV dbSNP153 33..33 33 - - - 102739 RMVar_ID_102739 Human_SNP_ID_80762829 m1A Human chr2 + 85639246 85639246 85639246 AAAAGAGCAGTTGCTCCATAATGACGAGTACCAGGAGACAATGGTGGAGTCCACTTTTATGTACC AAAAGAGCAGTTGCTCCATAATGACGAGTACCGGGAGACAATGGTGGAGTCCACTTTTATGTACC A G USP39 Ensembl:ENSG00000168883 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:85637429..85639295 32194978 MeRIP-seq:(Medium) rs372439936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1591078,Human_RBP_ID_22505979,Human_RBP_ID_26819954 Human_Splice_Rec_269092,Human_Splice_Rec_269128,Human_Splice_Rec_269150,Human_Splice_Rec_269186,Human_Splice_Rec_269216,Human_Splice_Rec_269242,Human_Splice_Rec_269274,Human_Splice_Rec_269296,Human_Splice_Rec_269306,Human_Splice_Rec_269310 RMVar_hsa_circ_334819,RMVar_hsa_circ_347953,RMVar_hsa_circ_101891,RMVar_hsa_circ_15778,RMVar_hsa_circ_201580,RMVar_hsa_circ_305879,RMVar_hsa_circ_365253,RMVar_hsa_circ_58140,RMVar_hsa_circ_201585,RMVar_hsa_circ_339293,RMVar_hsa_circ_355012,RMVar_hsa_circ_314808,RMVar_hsa_circ_60504,RMVar_hsa_circ_329853,RMVar_hsa_circ_201586 102740 RMVar_ID_102740 Human_SNP_ID_80791605 m1A Human chr2 - 85753920 85753920 85753920 CCGCTGCGCTCCATCTGTGTTTGTTTAGCCTCAGTTTACACAGAAGCCCAGTTCGCGAGATCAGT CCGCTGCGCTCCATCTGTGTTTGTTTAGCCTCGGTTTACACAGAAGCCCAGTTCGCGAGATCAGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85753870..85754014 26863196 MeRIP-seq:(Medium) rs1168046710 Functional Loss SNV dbSNP153 33..33 33 - - - 102741 RMVar_ID_102741 Human_SNP_ID_80791689 m1A Human chr2 + 85754121 85754121 85754121 GGGGGAGGGCGGGCGAAGCGGGAGAGCCAGAGACTCCTCGGCGCTGAGCGCGGCGGCGGCCCGGG GGGGGAGGGCGGGCGAAGCGGGAGAGCCAGAGCCTCCTCGGCGCTGAGCGCGGCGGCGGCCCGGG A C ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85751841..85754309 26863196 MeRIP-seq:(Medium) rs1248216295 Functional Loss SNV dbSNP153 33..33 33 - - - 102742 RMVar_ID_102742 Human_SNP_ID_80791690 m1A Human chr2 + 85754121 85754121 85754121 GGGGGAGGGCGGGCGAAGCGGGAGAGCCAGAGACTCCTCGGCGCTGAGCGCGGCGGCGGCCCGGG GGGGGAGGGCGGGCGAAGCGGGAGAGCCAGAGGCTCCTCGGCGCTGAGCGCGGCGGCGGCCCGGG A G ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85751841..85754309 26863196 MeRIP-seq:(Medium) rs1248216295 Functional Loss SNV dbSNP153 33..33 33 - - - 102743 RMVar_ID_102743 Human_SNP_ID_80791725 m1A Human chr2 + 85754190 85754190 85754190 CCCACGCCCCTGCCTCGCGCGCCGCCCGCGCCATGAAGCACATCCCGGTCCTCGAGGACGGGCCG CCCACGCCCCTGCCTCGCGCGCCGCCCGCGCCGTGAAGCACATCCCGGTCCTCGAGGACGGGCCG A G ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85754140..85754244 26863196 MeRIP-seq:(Medium) rs773364838 Functional Loss SNV dbSNP153 33..33 33 - - - 102744 RMVar_ID_102744 Human_SNP_ID_80792032 m1A Human chr2 + 85754696 85754696 85754696 CCGCCCGCGCGCCCCGCGCCGTCAGCACCCCCAGCACCGCCAGCGCCCCCGGAGTCCACTGTGCG CCGCCCGCGCGCCCCGCGCCGTCAGCACCCCCCGCACCGCCAGCGCCCCCGGAGTCCACTGTGCG A C ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85754646..85754775 26863196 MeRIP-seq:(Medium) rs183565439 Functional Loss SNV dbSNP153 33..33 33 - - - 102745 RMVar_ID_102745 Human_SNP_ID_80792114 m1A Human chr2 + 85754755 85754755 85754755 TGTGCGCCCTGCGCCCCCGACGCGCCCCGGGGAAAGTTCCTACTCGTCAATTTCACACGTAATTT TGTGCGCCCTGCGCCCCCGACGCGCCCCGGGGGAAGTTCCTACTCGTCAATTTCACACGTAATTT A G ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:85754487..85754775 26863196 MeRIP-seq:(Medium) rs527369972 Functional Loss SNV dbSNP153 33..33 33 - - - 102746 RMVar_ID_102746 Human_SNP_ID_80792119 m1A Human chr2 + 85754764 85754764 85754764 TGCGCCCCCGACGCGCCCCGGGGAAAGTTCCTACTCGTCAATTTCACACGTAATTTACAATAACC TGCGCCCCCGACGCGCCCCGGGGAAAGTTCCTCCTCGTCAATTTCACACGTAATTTACAATAACC A C ATOH8 Ensembl:ENSG00000168874 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:85754626..85754778 26863196 MeRIP-seq:(Medium) rs1262181828 Functional Loss SNV dbSNP153 33..33 33 - - - 102747 RMVar_ID_102747 Human_SNP_ID_80796918 m1A Human chr2 - 85773386 85773386 85773386 GGCTGGCTTCCAGTTGCCGGCCCTGCCCCAGGACCCCACAGCCCCTGACAGGCCACCCAGTGACT GGCTGGCTTCCAGTTGCCGGCCCTGCCCCAGGTCCCCACAGCCCCTGACAGGCCACCCAGTGACT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85773381..85773463 26863196 MeRIP-seq:(Medium) rs1203388192 Functional Loss SNV dbSNP153 33..33 33 - - - 102748 RMVar_ID_102748 Human_SNP_ID_80811576 m1A Human chr2 + 85836317 85836317 85836317 TGCAGTAAAGGAAACAATCAACAAGTCAAGAGACAATCCATGGAATGGGAGAAGATACTTGTGAA TGCAGTAAAGGAAACAATCAACAAGTCAAGAGGCAATCCATGGAATGGGAGAAGATACTTGTGAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:85836314..85836441 26863196 MeRIP-seq:(Medium) rs960730733 Functional Loss SNV dbSNP153 33..33 33 - - - 102749 RMVar_ID_102749 Human_SNP_ID_80811577 m1A Human chr2 + 85836317 85836317 85836317 TGCAGTAAAGGAAACAATCAACAAGTCAAGAGACAATCCATGGAATGGGAGAAGATACTTGTGAA TGCAGTAAAGGAAACAATCAACAAGTCAAGAGTCAATCCATGGAATGGGAGAAGATACTTGTGAA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:85836314..85836441 26863196 MeRIP-seq:(Medium) rs960730733 Functional Loss SNV dbSNP153 33..33 33 - - - 102750 RMVar_ID_102750 Human_SNP_ID_80823691 m1A Human chr2 - 85888905 85888905 85888905 GGCTGGCGGCCGGCCGGCGCCCCCTCATTAGTATGCGGACGAAGGCGGCGGGCTGCGCGGAGCGG GGCTGGCGGCCGGCCGGCGCCCCCTCATTAGTGTGCGGACGAAGGCGGCGGGCTGCGCGGAGCGG T C ST3GAL5 Ensembl:ENSG00000115525 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85888871..85888972 26863196 MeRIP-seq:(Medium) rs758088295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556792,Human_RBP_ID_4618575,Human_RBP_ID_9330543 Human_Splice_Rec_269555,Human_Splice_Rec_269637,Human_Splice_Rec_269651,Human_Splice_Rec_269665,Human_Splice_Rec_269677,Human_Splice_Rec_269711,Human_Splice_Rec_269731,Human_Splice_Rec_269831,Human_Splice_Rec_269845,Human_Splice_Rec_269857,Human_Splice_Rec_269869,Human_Splice_Rec_269883,Human_Splice_Rec_269893,Human_Splice_Rec_269907,Human_Splice_Rec_269917,Human_Splice_Rec_269933,Human_Splice_Rec_269949,Human_Splice_Rec_269973,Human_Splice_Rec_270001,Human_Splice_Rec_270013,Human_Splice_Rec_270027,Human_Splice_Rec_270039,Human_Splice_Rec_270055,Human_Splice_Rec_270069,Human_Splice_Rec_270107,Human_Splice_Rec_270123,Human_Splice_Rec_270199,Human_Splice_Rec_270205,Human_Splice_Rec_270243,Human_Splice_Rec_270255,Human_Splice_Rec_270269,Human_Splice_Rec_270277 102751 RMVar_ID_102751 Human_SNP_ID_80823710 m1A Human chr2 - 85888941 85888941 85888941 AGCGGCGCTGGGGGCGGGTGGGGGCGCGGGGTACCGGGCTGGCGGCCGGCCGGCGCCCCCTCATT AGCGGCGCTGGGGGCGGGTGGGGGCGCGGGGTTCCGGGCTGGCGGCCGGCCGGCGCCCCCTCATT T A ST3GAL5 Ensembl:ENSG00000115525 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85888896..85888989 26863196 MeRIP-seq:(Medium) rs1332848540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4618576,Human_RBP_ID_9330543 102752 RMVar_ID_102752 Human_SNP_ID_80823711 m1A Human chr2 - 85888941 85888941 85888941 AGCGGCGCTGGGGGCGGGTGGGGGCGCGGGGTACCGGGCTGGCGGCCGGCCGGCGCCCCCTCATT AGCGGCGCTGGGGGCGGGTGGGGGCGCGGGGTGCCGGGCTGGCGGCCGGCCGGCGCCCCCTCATT T C ST3GAL5 Ensembl:ENSG00000115525 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85888896..85888989 26863196 MeRIP-seq:(Medium) rs1332848540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4618576,Human_RBP_ID_9330543 102753 RMVar_ID_102753 Human_SNP_ID_80823736 m1A Human chr2 - 85888975 85888975 85888975 GGGGAGCGGCGGCCCCCAGCTGAATGGGCGCGAGAGCGGCGCTGGGGGCGGGTGGGGGCGCGGGG GGGGAGCGGCGGCCCCCAGCTGAATGGGCGCGGGAGCGGCGCTGGGGGCGGGTGGGGGCGCGGGG T C ST3GAL5 Ensembl:ENSG00000115525 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85888932..85888999 26863196 MeRIP-seq:(Medium) rs1180468833 Functional Loss SNV dbSNP153 33..33 33 - - - 102754 RMVar_ID_102754 Human_SNP_ID_80845138 m1A Human chr2 - 85979136 85979131 85979136 GAGGAAAGGTGAAAGAGAAATGCAGAAAGAGAAAAAAGAAAATAAAAGAGAGGAAAAGAGAAAGA GAGGAAAGGTGAAAGAGAAATGCAGAAAGAGA_____GAAAATAAAAGAGAGGAAAAGAGAAAGA CTTTTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85979039..85979153 26863196 MeRIP-seq:(Medium) rs1441500381 Functional Loss DEL dbSNP153 33..37 33 - - - 102755 RMVar_ID_102755 Human_SNP_ID_80856210 m1A Human chr2 - 86024926 86024926 86024926 CACCATGTTGGCCAGGCTAGTCTCGAACTCCTAATCTCAGGTGATCCGCCTGCCTCAGCCTCCCA CACCATGTTGGCCAGGCTAGTCTCGAACTCCTCATCTCAGGTGATCCGCCTGCCTCAGCCTCCCA T G POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs184310590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975162 102756 RMVar_ID_102756 Human_SNP_ID_80856261 m1A Human chr2 - 86025091 86025091 86025091 CACTTGTTACCCAGGCTGAGTGCAATGGCGCAATCTCGGCTCCACTGCAACCTCCATCTCCCGAG CACTTGTTACCCAGGCTGAGTGCAATGGCGCAGTCTCGGCTCCACTGCAACCTCCATCTCCCGAG T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1488998771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975163 102757 RMVar_ID_102757 Human_SNP_ID_80864522 m1A Human chr2 - 86056366 86056366 86056366 CTCACTGCAACCTCCAATTCCCTGGTTAAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCAATTCCCTGGTTAAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr2:86056363..86056445 26863410 MeRIP-seq:(Medium) rs546519091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109773,RMVar_hsa_circ_201599,RMVar_hsa_circ_79820,RMVar_hsa_circ_110958,RMVar_hsa_circ_201602,RMVar_hsa_circ_100661,RMVar_hsa_circ_201603,RMVar_hsa_circ_75776,RMVar_hsa_circ_104072,RMVar_hsa_circ_201604,RMVar_hsa_circ_6980,RMVar_hsa_circ_107918,RMVar_hsa_circ_201608,RMVar_hsa_circ_97960,RMVar_hsa_circ_201610,RMVar_hsa_circ_88507,RMVar_hsa_circ_201609,RMVar_hsa_circ_201607,RMVar_hsa_circ_98435,RMVar_hsa_circ_201614,RMVar_hsa_circ_92349,RMVar_hsa_circ_201611,RMVar_hsa_circ_201612,RMVar_hsa_circ_366262,RMVar_hsa_circ_20538,RMVar_hsa_circ_116842,RMVar_hsa_circ_201613,RMVar_hsa_circ_201616 102758 RMVar_ID_102758 Human_SNP_ID_80876931 m1A Human chr2 + 86106287 86106287 86106287 TTGTATCTGCTGTTCGCTGGCTGGGCCTCCGCAGCAGGCTTGGCCAGCCGCTGACGGGTCGGCGG TTGTATCTGCTGTTCGCTGGCTGGGCCTCCGCCGCAGGCTTGGCCAGCCGCTGACGGGTCGGCGG A C PTCD3 Ensembl:ENSG00000132300 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr2:86106226..86106375;chr2:86106226..86106397;chr2:86106226..86106396 26863196 MeRIP-seq:(Medium) rs762537111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556818,Human_RBP_ID_4618803,Human_RBP_ID_19002079,Human_RBP_ID_22449905 Human_Splice_Rec_270481,Human_Splice_Rec_270493,Human_Splice_Rec_270509,Human_Splice_Rec_270523,Human_Splice_Rec_270531,Human_Splice_Rec_270541,Human_Splice_Rec_270585,Human_Splice_Rec_270589 102759 RMVar_ID_102759 Human_SNP_ID_80876937 m1A Human chr2 - 86106294 86106294 86106294 AACCCGCCCGCCGACCCGTCAGCGGCTGGCCAAGCCTGCTGCGGAGGCCCAGCCAGCGAACAGCA AACCCGCCCGCCGACCCGTCAGCGGCTGGCCATGCCTGCTGCGGAGGCCCAGCCAGCGAACAGCA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:86106251..86106350 26863196 MeRIP-seq:(Medium) rs751363119 Functional Loss SNV dbSNP153 33..33 33 - - - 102760 RMVar_ID_102760 Human_SNP_ID_80876938 m1A Human chr2 - 86106294 86106294 86106294 AACCCGCCCGCCGACCCGTCAGCGGCTGGCCAAGCCTGCTGCGGAGGCCCAGCCAGCGAACAGCA AACCCGCCCGCCGACCCGTCAGCGGCTGGCCACGCCTGCTGCGGAGGCCCAGCCAGCGAACAGCA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:86106251..86106350 26863196 MeRIP-seq:(Medium) rs751363119 Functional Loss SNV dbSNP153 33..33 33 - - - 102761 RMVar_ID_102761 Human_SNP_ID_80885508 m1A Human chr2 - 86137996 86137996 86137996 CCTGAAATTGGGAAACTATTGACCCAACCCCAACTGTGTTAGAACTGCATGAACACCTAAGATGA CCTGAAATTGGGAAACTATTGACCCAACCCCACCTGTGTTAGAACTGCATGAACACCTAAGATGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:86137849..86138004 32194978 MeRIP-seq:(Medium) rs1037588660 Functional Loss SNV dbSNP153 33..33 33 - - - 102762 RMVar_ID_102762 Human_SNP_ID_80887239 m1A Human chr2 - 86144295 86144295 86144295 ATCCTGACAGCATATGCCAGCGCCGTAGGAATAGGAACCACTCAGGTGCAGCCAGAGTGAGGTTT ATCCTGACAGCATATGCCAGCGCCGTAGGAATGGGAACCACTCAGGTGCAGCCAGAGTGAGGTTT T C IMMT Ensembl:ENSG00000132305 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86144244..86144428 26863196 MeRIP-seq:(Medium) rs1214771418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556888,Human_RBP_ID_4618884,Human_RBP_ID_5197323,Human_RBP_ID_6955047,Human_RBP_ID_17392241 Human_miRNA_ID_2057197,Human_miRNA_ID_2750051 RMVar_hsa_circ_91890,RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201670,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672 102763 RMVar_ID_102763 Human_SNP_ID_80887276 m1A Human chr2 - 86144377 86144377 86144377 GCTGAAGGGGGAATCCAGACGAGTGGCACAGGACTGGCTGAAGGAAGCCCGAATGACCCTAGAAA GCTGAAGGGGGAATCCAGACGAGTGGCACAGGGCTGGCTGAAGGAAGCCCGAATGACCCTAGAAA T C IMMT Ensembl:ENSG00000132305 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:86144301..86151480 32194978 MeRIP-seq:(Medium) rs767253052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775621,Human_RBP_ID_1924315,Human_RBP_ID_6955049,Human_RBP_ID_13977644,Human_RBP_ID_17658540,Human_RBP_ID_17699735,Human_RBP_ID_22765924,Human_RBP_ID_27293111 Human_miRNA_ID_2579495 RMVar_hsa_circ_91890,RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201670,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672 102764 RMVar_ID_102764 Human_SNP_ID_80897035 m1A Human chr2 - 86181356 86181356 86181356 TGTTTTCCTTCTTTAGAGTTGTCTCTGTGGGAAGTTTGTCCTCCGTCCATTGCGACCATGCCGCA TGTTTTCCTTCTTTAGAGTTGTCTCTGTGGGACGTTTGTCCTCCGTCCATTGCGACCATGCCGCA T G IMMT Ensembl:ENSG00000132305 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86181301..86181421 26863196 MeRIP-seq:(Medium) rs1337737385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4618950,Human_RBP_ID_19002097,Human_RBP_ID_22452368,Human_RBP_ID_26818724 Human_Splice_Rec_270690,Human_Splice_Rec_270691,Human_Splice_Rec_270718,Human_Splice_Rec_270719,Human_Splice_Rec_270746,Human_Splice_Rec_270747,Human_Splice_Rec_270794,Human_Splice_Rec_270795,Human_Splice_Rec_270822,Human_Splice_Rec_270823,Human_Splice_Rec_270848,Human_Splice_Rec_270849,Human_Splice_Rec_270860,Human_Splice_Rec_270861,Human_Splice_Rec_270886,Human_Splice_Rec_270887,Human_Splice_Rec_270904,Human_Splice_Rec_270905 RMVar_hsa_circ_30117,RMVar_hsa_circ_54440,RMVar_hsa_circ_311763 102765 RMVar_ID_102765 Human_SNP_ID_80900393 m1A Human chr2 + 86195192 86195192 86195192 TCCCAGTCCGGCGAACTCCCTGGTGGCTGCCTAGCTGCCCGCCCGGGCCTCTCCCGACGAGGGTG TCCCAGTCCGGCGAACTCCCTGGTGGCTGCCTGGCTGCCCGCCCGGGCCTCTCCCGACGAGGGTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:86195190..86195338 26863196 MeRIP-seq:(Medium) rs1278141725 Functional Loss SNV dbSNP153 33..33 33 - - - 102766 RMVar_ID_102766 Human_SNP_ID_80900495 m1A Human chr2 + 86195391 86195391 86195391 CGATAACTGACAGGCCCGCAGCATCTCGGTCAAGCGGACGGCGCTGCTGGTGGACTCGAGCTGCC CGATAACTGACAGGCCCGCAGCATCTCGGTCAGGCGGACGGCGCTGCTGGTGGACTCGAGCTGCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:86181326..86195475 26863410 MeRIP-seq:(Medium) rs1438659185 Functional Loss SNV dbSNP153 33..33 33 - - - 102767 RMVar_ID_102767 Human_SNP_ID_80900513 m1A Human chr2 - 86195406 86195406 86195406 AACTCGCGCCGCCGCGGCAGCTCGAGTCCACCAGCAGCGCCGTCCGCTTGACCGAGATGCTGCGG AACTCGCGCCGCCGCGGCAGCTCGAGTCCACCGGCAGCGCCGTCCGCTTGACCGAGATGCTGCGG T C IMMT Ensembl:ENSG00000132305 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86195296..86195450 26863196 MeRIP-seq:(Medium) rs371237578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556920,Human_RBP_ID_4618965,Human_RBP_ID_8851982,Human_RBP_ID_18422752,Human_RBP_ID_26818728 Human_Splice_Rec_270717,Human_Splice_Rec_270745,Human_Splice_Rec_270793,Human_Splice_Rec_270821,Human_Splice_Rec_270847,Human_Splice_Rec_270859,Human_Splice_Rec_270885,Human_Splice_Rec_270903 102768 RMVar_ID_102768 Human_SNP_ID_80901769 m1A Human chr2 + 86199532 86199532 86199532 TCTGCCTTTGCTGGTGCAGTGAGAGCAGCTTCAGGTCAGTGGAGAGCGACATACTCCATGCATGC TCTGCCTTTGCTGGTGCAGTGAGAGCAGCTTCGGGTCAGTGGAGAGCGACATACTCCATGCATGC A G MRPL35 Ensembl:ENSG00000132313 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:86199517..86199587 26863196 MeRIP-seq:(Medium) rs1210108846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918352,Human_RBP_ID_4623468,Human_RBP_ID_19097853 Human_Splice_Rec_270909,Human_Splice_Rec_270917,Human_Splice_Rec_270921,Human_Splice_Rec_270927 RMVar_hsa_circ_122945,RMVar_hsa_circ_201683 102769 RMVar_ID_102769 Human_SNP_ID_80932996 m1A Human chr2 - 86337559 86337558 86337559 CCGGGAACGCCGCAGCAGCCCGCGCCGCCCGCAGCCTAGCCGAGCCGCGCCGCCCGGGCCTCGCC CCGGGAACGCCGCAGCAGCCCGCGCCGCCCGC_GCCTAGCCGAGCCGCGCCGCCCGGGCCTCGCC CT C REEP1 Ensembl:ENSG00000068615 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:86337516..86337601 26863196 MeRIP-seq:(Medium) rs1553472251 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_270935,Human_Splice_Rec_270951,Human_Splice_Rec_271009,Human_Splice_Rec_271019 102770 RMVar_ID_102770 Human_SNP_ID_80957007 m1A Human chr2 - 86441446 86441446 86441446 CCTCTCCCCGCAGCCGAGGCCGCGGCGCTCTTACCCCGCCTCCCGCCTCCCTGAGTCACCGGCGG CCTCTCCCCGCAGCCGAGGCCGCGGCGCTCTTCCCCCGCCTCCCGCCTCCCTGAGTCACCGGCGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:86441397..86441704;chr2:86441407..86441525 26863196 MeRIP-seq:(Medium) rs1407761743 Functional Loss SNV dbSNP153 33..33 33 - - - 102771 RMVar_ID_102771 Human_SNP_ID_80957319 m1A Human chr2 + 86442048 86442048 86442048 AGGGAGGAGCTCTTCCTGCAGGCGTGGAAACCATGGTGCTCACGCTCGGAGAAAGTTGGCCGGTA AGGGAGGAGCTCTTCCTGCAGGCGTGGAAACCGTGGTGCTCACGCTCGGAGAAAGTTGGCCGGTA A G KDM3A Ensembl:ENSG00000115548 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:86442026..86442153 26863196 MeRIP-seq:(Medium) rs768071670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918356,Human_RBP_ID_4619032,Human_RBP_ID_9428746,Human_RBP_ID_18422267,Human_RBP_ID_19097857,Human_RBP_ID_26339527 Human_Splice_Rec_271064,Human_Splice_Rec_271072,Human_Splice_Rec_271120,Human_Splice_Rec_271168,Human_Splice_Rec_271208 Human_miRNA_ID_2299240,Human_miRNA_ID_2302511,Human_miRNA_ID_2305775 RMVar_hsa_circ_10475,RMVar_hsa_circ_348353,RMVar_hsa_circ_352723,RMVar_hsa_circ_201692,RMVar_hsa_circ_201693 102772 RMVar_ID_102772 Human_SNP_ID_80974497 m1A Human chr2 - 86505951 86505951 86505951 CAATGTGGTGTTCATCTTTGCTCTTTCTTTTCAGGGGCCTTGGGCAAAGCACCCAGTAAAGTGAC CAATGTGGTGTTCATCTTTGCTCTTTCTTTTCGGGGGCCTTGGGCAAAGCACCCAGTAAAGTGAC T C CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:86505909..86507536 26863196 MeRIP-seq:(Medium) rs1365405708 Functional Loss SNV dbSNP153 33..33 33 - - - 102773 RMVar_ID_102773 Human_SNP_ID_80975514 m1A Human chr2 - 86510390 86510390 86510390 AAAGTCTTGTGAAGATTCCAGAGATTCAGGCCACCATGAGGGAGTTGTCCAAAGAAATGATGAAG AAAGTCTTGTGAAGATTCCAGAGATTCAGGCCGCCATGAGGGAGTTGTCCAAAGAAATGATGAAG T C CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86510318..86510390 26863196 MeRIP-seq:(Medium) rs770818481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557089,Human_RBP_ID_17962745,Human_RBP_ID_23888040 Human_Splice_Rec_271310,Human_Splice_Rec_271311,Human_Splice_Rec_271319,Human_Splice_Rec_271326,Human_Splice_Rec_271327,Human_Splice_Rec_271336,Human_Splice_Rec_271337,Human_Splice_Rec_271346,Human_Splice_Rec_271347,Human_Splice_Rec_271351,Human_Splice_Rec_271358,Human_Splice_Rec_271376,Human_Splice_Rec_271377,Human_Splice_Rec_271386 RMVar_hsa_circ_201706,RMVar_hsa_circ_300329,RMVar_hsa_circ_359267 102774 RMVar_ID_102774 Human_SNP_ID_80979642 m1A Human chr2 + 86529304 86529304 86529304 ACAGCTTGCTCACAGCCTTCCTTGACCTGATCATCTCCTTGGCCAGAACTATGCAGACATCCTTC ACAGCTTGCTCACAGCCTTCCTTGACCTGATCGTCTCCTTGGCCAGAACTATGCAGACATCCTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:86529254..86540650 32194978 MeRIP-seq:(Medium) rs745732049 Functional Loss SNV dbSNP153 33..33 33 - - - 102775 RMVar_ID_102775 Human_SNP_ID_81024564 m1A Human chr2 - 86720603 86720603 86720603 CCAGGTGTCCGCAGCCGTTCGGCCCGGGCCCCACCGAGGCCGCGTCCTGCTCCTCGTTCCCCAAG CCAGGTGTCCGCAGCCGTTCGGCCCGGGCCCCGCCGAGGCCGCGTCCTGCTCCTCGTTCCCCAAG T C RNF103-CHMP3 Ensembl:ENSG00000249884 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:86720560..86720647 26863196 MeRIP-seq:(Medium) rs71222447 Functional Loss SNV dbSNP153 33..33 33 - - - 102776 RMVar_ID_102776 Human_SNP_ID_81162761 m1A Human chr2 - 87348773 87348755 87348773 CGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGCGAGGCGCGCAGCGG CGGCGGCGCGGCGGAGAGACGGACAGCGGCGG__________________CGAGGCGCGCAGCGG GCCGCCGCTGTCTGCCTCT G lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:87348681..87348870 26863196 MeRIP-seq:(Medium) rs1189366963 Functional Loss DEL dbSNP153 33..50 33 - - - 102777 RMVar_ID_102777 Human_SNP_ID_81162781 m1A Human chr2 - 87348787 87348769 87348787 GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGC GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAG__________________GCAGACAGCGGCGGC CCTCTCCGCCGCTGTCCGT C lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:87348709..87348851;chr2:87348725..87348850;chr2:87348718..87348960;chr2:87348714..87348850 26863196 MeRIP-seq:(Medium) rs1374174108 Functional Loss DEL dbSNP153 33..50 33 - - - 102778 RMVar_ID_102778 Human_SNP_ID_81162783 m1A Human chr2 - 87348773 87348773 87348773 CGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGCGAGGCGCGCAGCGG CGGCGGCGCGGCGGAGAGACGGACAGCGGCGGCGAGGCAGACAGCGGCGGCGAGGCGCGCAGCGG T G lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:87348681..87348870 26863196 MeRIP-seq:(Medium) rs1330475984 Functional Loss SNV dbSNP153 33..33 33 - - - 102779 RMVar_ID_102779 Human_SNP_ID_81162798 m1A Human chr2 - 87348787 87348787 87348787 GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGC GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCAGACAGCGGCGGC T C lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:87348709..87348851;chr2:87348725..87348850;chr2:87348718..87348960;chr2:87348714..87348850 26863196 MeRIP-seq:(Medium) rs62145313 Functional Loss SNV dbSNP153 33..33 33 - - - 102780 RMVar_ID_102780 Human_SNP_ID_81162799 m1A Human chr2 - 87348787 87348787 87348787 GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGC GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGCCGGACAGCGGCGGAGAGGCAGACAGCGGCGGC T G lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:87348709..87348851;chr2:87348725..87348850;chr2:87348718..87348960;chr2:87348714..87348850 26863196 MeRIP-seq:(Medium) rs62145313 Functional Loss SNV dbSNP153 33..33 33 - - - 102781 RMVar_ID_102781 Human_SNP_ID_81209502 m1A Human chr2 + 87476944 87476943 87476944 TTGGACTCACTATGGGTGCTCATGAAGGAGGCAGCATTTGGACAAGGCCCTGAGAGGCAGGTGGA TTGGACTCACTATGGGTGCTCATGAAGGAGGC_GCATTTGGACAAGGCCCTGAGAGGCAGGTGGA CA C AC133644.2,CYTOR Ensembl:ENSG00000284879,Ensembl:ENSG00000222041 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:87476942..87477060 26863196 MeRIP-seq:(Medium) rs568107735 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5590750 102782 RMVar_ID_102782 Human_SNP_ID_81220138 m1A Human chr2 + 87521327 87521327 87521327 CCTCTACCTGTTGCCCGCCGATCACAGCCGGAATGCAGCTGAAAGATTCCCTGGGGCCTGGTTCC CCTCTACCTGTTGCCCGCCGATCACAGCCGGAGTGCAGCTGAAAGATTCCCTGGGGCCTGGTTCC A G AC133644.2,CYTOR Ensembl:ENSG00000284879,Ensembl:ENSG00000222041 lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:87521276..87521400 32194978 MeRIP-seq:(Medium) rs994094879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5590136 RMVar_hsa_circ_121863,RMVar_hsa_circ_201730 102783 RMVar_ID_102783 Human_SNP_ID_81220153 m1A Human chr2 + 87521368 87521368 87521368 AAAGATTCCCTGGGGCCTGGTTCCAACCGCCCACTGTGGACTCTGAGGCCTCTGCATTTGCGGGT AAAGATTCCCTGGGGCCTGGTTCCAACCGCCCGCTGTGGACTCTGAGGCCTCTGCATTTGCGGGT A G AC133644.2,CYTOR Ensembl:ENSG00000284879,Ensembl:ENSG00000222041 lincRNA,lincRNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:87521276..87521475 32194978 MeRIP-seq:(Medium) rs1459685484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557298,Human_RBP_ID_4625787,Human_RBP_ID_5590136,Human_RBP_ID_8526774 Human_miRNA_ID_1994493,Human_miRNA_ID_2226988,Human_miRNA_ID_2271342,Human_miRNA_ID_2502965,Human_miRNA_ID_3149688,Human_miRNA_ID_3163080,Human_miRNA_ID_3165594,Human_miRNA_ID_3179418 RMVar_hsa_circ_121863,RMVar_hsa_circ_201730 102784 RMVar_ID_102784 Human_SNP_ID_81327452 m1A Human chr2 + 88017096 88017096 88017096 CGCGATGGGGACCAGGGCGGCGGGCCGCAGCCAGGGTGTGGGTGGGCGACGGTCAAGGTGCCTTG CGCGATGGGGACCAGGGCGGCGGGCCGCAGCCGGGGTGTGGGTGGGCGACGGTCAAGGTGCCTTG A G AC108479.1 Ensembl:ENSG00000287670 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:88017046..88017273 26863196 MeRIP-seq:(Medium) rs1005538684 Functional Loss SNV dbSNP153 33..33 33 - - - 102785 RMVar_ID_102785 Human_SNP_ID_81329914 m1A Human chr2 - 88027877 88027874 88027878 GAGAAAAAAAGCCGAGATGTAGTCTCTAAGAAAGAGGAACGTAAGCGTACAAAAAAGAAAAAGGA GAGAAAAAAAGCCGAGATGTAGTCTCTAAGA____GGAACGTAAGCGTACAAAAAAGAAAAAGGA CTCTT C KRCC1 Ensembl:ENSG00000172086 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:88027826..88028075 26863196 MeRIP-seq:(Medium) rs1213160099 Functional Loss DEL dbSNP153 32..35 33 - - - 102786 RMVar_ID_102786 Human_SNP_ID_81336421 m1A Human chr2 - 88055289 88055289 88055289 TCAGGGAAAGGGAAGTGGGGTGAGGAAACTCGAAAATTGAGGGGACAGGGATAAATAGAGAAAAG TCAGGGAAAGGGAAGTGGGGTGAGGAAACTCGCAAATTGAGGGGACAGGGATAAATAGAGAAAAG T G KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:88055053..88055447 26863196 MeRIP-seq:(Medium) rs917317315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10008798,Human_RBP_ID_23282709 102787 RMVar_ID_102787 Human_SNP_ID_81479309 m1A Human chr2 + 88627399 88627399 88627399 AGGGACCCTACTGCCGCCCCGACGGCCTGGACAGCCAGCCGTGTTCCCCTGGCCACGTCTCAGCC AGGGACCCTACTGCCGCCCCGACGGCCTGGACTGCCAGCCGTGTTCCCCTGGCCACGTCTCAGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:88626946..88627438 26863196 MeRIP-seq:(Medium) rs1558669120 Functional Loss SNV dbSNP153 33..33 33 - - - 102788 RMVar_ID_102788 Human_SNP_ID_81479320 m1A Human chr2 - 88627426 88627426 88627426 TCACTCAGGTGGCAGCGGCAGAGGCCGGGCTGAGACGTGGCCAGGGGAACACGGCTGGCTGTCCA TCACTCAGGTGGCAGCGGCAGAGGCCGGGCTGGGACGTGGCCAGGGGAACACGGCTGGCTGTCCA T C EIF2AK3 Ensembl:ENSG00000172071 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:88626977..88627476 26863196 MeRIP-seq:(Medium) rs1161772940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4619579,Human_RBP_ID_18421844 102789 RMVar_ID_102789 Human_SNP_ID_81493948 m1A Human chr2 - 88691777 88691777 88691777 CGGGAGGTCCCAGCTGTTCCCTCCTCCGCCGGAGGCCGCGCCCCCGGCCCTCCCGGGCAGCGGGG CGGGAGGTCCCAGCTGTTCCCTCCTCCGCCGGGGGCCGCGCCCCCGGCCCTCCCGGGCAGCGGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:88691676..88691894 26863410 MeRIP-seq:(Medium) rs760833833 Functional Loss SNV dbSNP153 33..33 33 - - - 102790 RMVar_ID_102790 Human_SNP_ID_81494005 m1A Human chr2 - 88691891 88691891 88691891 CATCGTGGAGGGGGCCGGGCAGATGCTGTTGGAGTCCCCGCAGCTGGTGCTTGTGTTGCCAGCAC CATCGTGGAGGGGGCCGGGCAGATGCTGTTGGTGTCCCCGCAGCTGGTGCTTGTGTTGCCAGCAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:88691743..88698543 32194978 MeRIP-seq:(Medium) rs1391408848 Functional Loss SNV dbSNP153 33..33 33 - - - 102791 RMVar_ID_102791 Human_SNP_ID_81503263 m1A Human chr2 + 88733212 88733212 88733212 AACCACAGGAACAGCTCCATGTGGGCAAATGGACACTGCTCGGACTGGCTGGGGTGATAGGACAG AACCACAGGAACAGCTCCATGTGGGCAAATGGGCACTGCTCGGACTGGCTGGGGTGATAGGACAG A G RPIA Ensembl:ENSG00000153574 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:88733193..88733324 26863196 MeRIP-seq:(Medium) rs894072914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6956609 RMVar_hsa_circ_323965 102792 RMVar_ID_102792 Human_SNP_ID_81768153 m1A Human chr2 + 89826451 89826451 89826451 CGGGTTGATTCCAATCCATTCCATTCCATTGCATTCCATTCCATTCCTTTCCATTCCATTGCATT CGGGTTGATTCCAATCCATTCCATTCCATTGCGTTCCATTCCATTCCTTTCCATTCCATTGCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89826403..89826528 26863196 MeRIP-seq:(Medium) rs1185542717 Functional Loss SNV dbSNP153 33..33 33 - - - 102793 RMVar_ID_102793 Human_SNP_ID_81770349 m1A Human chr2 - 89829216 89829216 89829216 GAATGGAATGGAATCAACCTGATTGGAATGGAATGGAATGGAATGGAATGGAATCAACCCGAGTG GAATGGAATGGAATCAACCTGATTGGAATGGAGTGGAATGGAATGGAATGGAATCAACCCGAGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89829169..89829286 26863196 MeRIP-seq:(Medium) rs1165913326 Functional Loss SNV dbSNP153 33..33 33 - - - 102794 RMVar_ID_102794 Human_SNP_ID_81773375 m1A Human chr2 - 89832797 89832797 89832797 CAACCCGAGAGGAATGGAATGGAATGGAATGGAATGGAATAGAATTGAATGGGATGGAATGGAAT CAACCCGAGAGGAATGGAATGGAATGGAATGGTATGGAATAGAATTGAATGGGATGGAATGGAAT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89832790..89832931 26863196 MeRIP-seq:(Medium) rs796568461 Functional Loss SNV dbSNP153 33..33 33 - - - 102795 RMVar_ID_102795 Human_SNP_ID_81777854 m1A Human chr2 + 89838486 89838486 89838486 GAATGGAATGGAATTGCATCAACACGAGTGGAATGGAATGGAATTGAATGGAATTTATTGGAATG GAATGGAATGGAATTGCATCAACACGAGTGGAGTGGAATGGAATTGAATGGAATTTATTGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89838484..89838759 26863196 MeRIP-seq:(Medium) rs1212888104 Functional Loss SNV dbSNP153 33..33 33 - - - 102796 RMVar_ID_102796 Human_SNP_ID_81779367 m1A Human chr2 + 89840343 89840343 89840343 GAATGGAATGGAATGGAACGGAACGGAATGGAATGGAATGGAATGGAATGCAATCAACCCGAGTG GAATGGAATGGAATGGAACGGAACGGAATGGAGTGGAATGGAATGGAATGCAATCAACCCGAGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89840312..89840568 26863196 MeRIP-seq:(Medium) rs985225502 Functional Loss SNV dbSNP153 33..33 33 - - - 102797 RMVar_ID_102797 Human_SNP_ID_81780047 m1A Human chr2 - 89841113 89841104 89841114 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCGTGTTGATTCCATTCCATTCCATT CCATTCCATTCCATTCCATTCCATTCCATTC__________GTGTTGATTCCATTCCATTCCATT CGAATGGAATG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89840949..89841129 26863196 MeRIP-seq:(Medium) rs1263622489 Functional Loss DEL dbSNP153 32..41 33 - - - 102798 RMVar_ID_102798 Human_SNP_ID_81780048 m1A Human chr2 - 89841113 89841104 89841114 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCGTGTTGATTCCATTCCATTCCATT CCATTCCATTCCATTCCATTCCATTCCATTC_____CATTCGTGTTGATTCCATTCCATTCCATT CGAATGGAATG CGAATG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89840949..89841129 26863196 MeRIP-seq:(Medium) rs1263622489 Functional Loss DEL dbSNP153 32..36 33 - - - 102799 RMVar_ID_102799 Human_SNP_ID_48183424 m1A Human chr1 - 210233688 210233688 210233688 TAGGGCCGAAGAGGCGGGAGGGGAGGAAGGGAAGCGAGAGGCGGAGGCGTGGACCAGGCGGGCAG TAGGGCCGAAGAGGCGGGAGGGGAGGAAGGGAGGCGAGAGGCGGAGGCGTGGACCAGGCGGGCAG T C SERTAD4-AS1 Ensembl:ENSG00000203706 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:210233607..210233898 26863196 MeRIP-seq:(Medium) rs1324333323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17066445 Human_Splice_Rec_184309 102800 RMVar_ID_102800 Human_SNP_ID_48206255 m1A Human chr1 + 210328893 210328884 210328893 AGAGCGCCGCGGGTTCCCGAGTCCGGGCGCGGAGGGCGCGCGGGCACGGCGGCAGGGGCGTGCTC AGAGCGCCGCGGGTTCCCGAGTCC_________GGGCGCGCGGGCACGGCGGCAGGGGCGTGCTC CGGGCGCGGA C HHAT Ensembl:ENSG00000054392 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:210328890..210328974 26863196 MeRIP-seq:(Medium) rs1290078315 Functional Loss DEL dbSNP153 25..33 33 - - - 102801 RMVar_ID_102801 Human_SNP_ID_48206263 m1A Human chr1 + 210328893 210328893 210328893 AGAGCGCCGCGGGTTCCCGAGTCCGGGCGCGGAGGGCGCGCGGGCACGGCGGCAGGGGCGTGCTC AGAGCGCCGCGGGTTCCCGAGTCCGGGCGCGGGGGGCGCGCGGGCACGGCGGCAGGGGCGTGCTC A G HHAT Ensembl:ENSG00000054392 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:210328890..210328974 26863196 MeRIP-seq:(Medium) rs1388508815 Functional Loss SNV dbSNP153 33..33 33 - - - 102802 RMVar_ID_102802 Human_SNP_ID_48250654 m1A Human chr1 - 210503769 210503769 210503769 TGGACACATTTGCCAAATGAAAGGTCACCGGCAACTTTGAGGAGTAGCTTCATTGAGTGGGGGAA TGGACACATTTGCCAAATGAAAGGTCACCGGCTACTTTGAGGAGTAGCTTCATTGAGTGGGGGAA T A HSALNG0010255 RNACentral:URS0000EAC21A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:210503576..210503800 26863196 MeRIP-seq:(Medium) rs1558041740 Functional Loss SNV dbSNP153 33..33 33 - - - 102803 RMVar_ID_102803 Human_SNP_ID_48250729 m1A Human chr1 - 210504093 210504093 210504093 ATTGGATGTGTAATTTGCAAATATTTTCTCTCAACCTATAGCTTATCTTTTCATTTTCTGAAAAT ATTGGATGTGTAATTTGCAAATATTTTCTCTCGACCTATAGCTTATCTTTTCATTTTCTGAAAAT T C HSALNG0010255 RNACentral:URS0000EAC21A lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:210504090..210504189 26863196 MeRIP-seq:(Medium) rs150303538 Functional Loss SNV dbSNP153 33..33 33 - - - 102804 RMVar_ID_102804 Human_SNP_ID_48434082 m1A Human chr1 + 211259616 211259616 211259616 GCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGGCGGCGGCG GCCCGAGTTACTGGGGAAGAACCGATCGGCCACCGGCAGCGCCAAGAGCCCGGCAGGCGGCGGCG A C RCOR3 Ensembl:ENSG00000117625 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211259390..211259696 26863196 MeRIP-seq:(Medium) rs780946230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223785,Human_RBP_ID_17737307 Human_Splice_Rec_184796 102805 RMVar_ID_102805 Human_SNP_ID_48434083 m1A Human chr1 + 211259616 211259616 211259616 GCCCGAGTTACTGGGGAAGAACCGATCGGCCAACGGCAGCGCCAAGAGCCCGGCAGGCGGCGGCG GCCCGAGTTACTGGGGAAGAACCGATCGGCCAGCGGCAGCGCCAAGAGCCCGGCAGGCGGCGGCG A G RCOR3 Ensembl:ENSG00000117625 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211259390..211259696 26863196 MeRIP-seq:(Medium) rs780946230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223785,Human_RBP_ID_17737307 Human_Splice_Rec_184796 102806 RMVar_ID_102806 Human_SNP_ID_48434230 m1A Human chr1 - 211259893 211259885 211259893 GCAAAGGCGGAGGATTGGTCGAGGGCGGAGGGACGGGGGGTCGCGGGGGTGCTGCTGCACTGCAC GCAAAGGCGGAGGATTGGTCGAGGGCGGAGGG________TCGCGGGGGTGCTGCTGCACTGCAC ACCCCCCGT A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:211259876..211260009 26863196 MeRIP-seq:(Medium) rs1170978132 Functional Loss DEL dbSNP153 33..40 33 - - - 102807 RMVar_ID_102807 Human_SNP_ID_48447214 m1A Human chr1 - 211313483 211313483 211313483 TTCAGAGTGGCAATAGGGGCTGTTGGTGTTGGAGTGGATGATGGGGCAGGAGGTGATGGACCCAG TTCAGAGTGGCAATAGGGGCTGTTGGTGTTGGGGTGGATGATGGGGCAGGAGGTGATGGACCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:211313433..211313617 26863196 MeRIP-seq:(Medium) rs760116780 Functional Loss SNV dbSNP153 33..33 33 - - - 102808 RMVar_ID_102808 Human_SNP_ID_48450148 m1A Human chr1 + 211326882 211326882 211326882 CTGCAGACCGGCCTCGCGGAGCCCGCGCGCCGAGCCCCACGTGAGTCCGGCGGGTCGCCGCCCTG CTGCAGACCGGCCTCGCGGAGCCCGCGCGCCGGGCCCCACGTGAGTCCGGCGGGTCGCCGCCCTG A G TRAF5 Ensembl:ENSG00000082512 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:211326854..211326934 26863196 MeRIP-seq:(Medium) rs1487859408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_185005,Human_Splice_Rec_185017,Human_Splice_Rec_185019 102809 RMVar_ID_102809 Human_SNP_ID_48451226 m1A Human chr1 - 211332057 211332057 211332057 TCATCCCAGCTTATCCCACCATACCCTGTCCCAGCCCAGCTTCCCTACCCTGGCCCCTGAGGTCT TCATCCCAGCTTATCCCACCATACCCTGTCCCTGCCCAGCTTCCCTACCCTGGCCCCTGAGGTCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211332053..211332182 26863196 MeRIP-seq:(Medium) rs1433616163 Functional Loss SNV dbSNP153 33..33 33 - - - 102810 RMVar_ID_102810 Human_SNP_ID_48452005 m1A Human chr1 - 211335676 211335676 211335676 TTCCTCTCTCCCCACCTCTTGCTGAGCTAAACACATACAAGCCCAGATGAAGCCTCACATATGCA TTCCTCTCTCCCCACCTCTTGCTGAGCTAAACTCATACAAGCCCAGATGAAGCCTCACATATGCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211335675..211335778 26863196 MeRIP-seq:(Medium) rs539099339 Functional Loss SNV dbSNP153 33..33 33 - - - 102811 RMVar_ID_102811 Human_SNP_ID_48452413 m1A Human chr1 + 211337362 211337362 211337362 GGAAAAGCAAGCAGAAGCCTCTTCTGCTGTTCAAGAAGACGCAAGGCAGTGTTGCCAGAGTGAGT GGAAAAGCAAGCAGAAGCCTCTTCTGCTGTTCGAGAAGACGCAAGGCAGTGTTGCCAGAGTGAGT A G TRAF5 Ensembl:ENSG00000082512 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211337359..211337885 26863196 MeRIP-seq:(Medium) rs1267426513 Functional Loss SNV dbSNP153 33..33 33 - - - 102812 RMVar_ID_102812 Human_SNP_ID_48459288 m1A Human chr1 - 211367627 211367627 211367627 CTTGGTTAATATCATTACCATGTCCCCTCCCTACTCAGCTTTCTGCATGTCATTTACAACCTCAG CTTGGTTAATATCATTACCATGTCCCCTCCCTGCTCAGCTTTCTGCATGTCATTTACAACCTCAG T C lnc-RD3-1 RNACentral:URS00008B9008 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211367576..211367722 26863196 MeRIP-seq:(Medium) rs1219629618 Functional Loss SNV dbSNP153 33..33 33 - - - 102813 RMVar_ID_102813 Human_SNP_ID_48459401 m1A Human chr1 + 211368211 211368210 211368211 ATGTGAATGGGTTTGAGGCTGAAAGTGTAGCCAGGGGCAGGTCACGTAGGGCCCAGTGTCACCTG ATGTGAATGGGTTTGAGGCTGAAAGTGTAGCC_GGGGCAGGTCACGTAGGGCCCAGTGTCACCTG CA C TRAF5 Ensembl:ENSG00000082512 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:211368044..211368239;chr1:211368025..211368280 26863196 MeRIP-seq:(Medium) rs1017434278 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23360420 RMVar_hsa_circ_18543 102814 RMVar_ID_102814 Human_SNP_ID_48511790 m1A Human chr1 + 211579123 211579123 211579123 CGGATGGCTGAGGAGCTAGAGAGGCGGCGGCCACGGCAGCTGCACTCGGCCCGGTCTCGGGCGCC CGGATGGCTGAGGAGCTAGAGAGGCGGCGGCCGCGGCAGCTGCACTCGGCCCGGTCTCGGGCGCC A G lnc-TRAF5-11 RNACentral:URS00008B9E0B lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:211579076..211579125 26863196 MeRIP-seq:(Medium) rs1024318962 Functional Loss SNV dbSNP153 33..33 33 - - - 102815 RMVar_ID_102815 Human_SNP_ID_48534886 m1A Human chr1 - 211675518 211675518 211675518 CTGGTCCCTGGAGCTCCGCACTTGGCGGCGCAACCTGCGTGAGGCAGCGCGACTCTGGCGACTGG CTGGTCCCTGGAGCTCCGCACTTGGCGGCGCAGCCTGCGTGAGGCAGCGCGACTCTGGCGACTGG T C NEK2 Ensembl:ENSG00000117650 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:211675429..211675600 26863410 MeRIP-seq:(Medium) rs764789276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4074735,Human_RBP_ID_5458564,Human_RBP_ID_8962336,Human_RBP_ID_9320344,Human_RBP_ID_23360581,Human_RBP_ID_26799422 102816 RMVar_ID_102816 Human_SNP_ID_48549206 m1A Human chr1 + 211735403 211735403 211735403 CGTGCCACCTCCTTCATCTGGCCAGCTCCCCAATCCCGGGCTGTCTGGTCCCCTGCTGTCTGGCT CGTGCCACCTCCTTCATCTGGCCAGCTCCCCAGTCCCGGGCTGTCTGGTCCCCTGCTGTCTGGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211735384..211735511 26863196 MeRIP-seq:(Medium) rs1477575792 Functional Loss SNV dbSNP153 33..33 33 - - - 102817 RMVar_ID_102817 Human_SNP_ID_48551579 m1A Human chr1 + 211745689 211745689 211745689 ACCCTCAGCTTATTCCCAGGGTCCAGTTCCTAATTGTTGGGGATTGGCGCAAAATGATTACAATA ACCCTCAGCTTATTCCCAGGGTCCAGTTCCTATTTGTTGGGGATTGGCGCAAAATGATTACAATA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:211745638..211745719 32194978 MeRIP-seq:(Medium) rs1159354913 Functional Loss SNV dbSNP153 33..33 33 - - - 102818 RMVar_ID_102818 Human_SNP_ID_48567018 m1A Human chr1 - 211815238 211815238 211815238 TGAGAGGAAAGATTTTAAAAATTTAAAAATTTAGCATAGGGTAGATGAAAAACATCCAAGTGGAG TGAGAGGAAAGATTTTAAAAATTTAAAAATTTGGCATAGGGTAGATGAAAAACATCCAAGTGGAG T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211815235..211815460 26863196 MeRIP-seq:(Medium) rs1283948996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 102819 RMVar_ID_102819 Human_SNP_ID_48570350 m1A Human chr1 + 211830216 211830216 211830216 TCGGCGGGCGCGGACGGCGGGCGGCTGCGGAGAGCGGGGGCGGGTGTCCCCCGCCGAGGGGTCGC TCGGCGGGCGCGGACGGCGGGCGGCTGCGGAGCGCGGGGGCGGGTGTCCCCCGCCGAGGGGTCGC A C LPGAT1-AS1 Ensembl:ENSG00000229258 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211830198..211830295 26863196 MeRIP-seq:(Medium) rs976941260 Functional Loss SNV dbSNP153 33..33 33 - - - 102820 RMVar_ID_102820 Human_SNP_ID_48570503 m1A Human chr1 - 211830663 211830663 211830663 GCGCCACAGCCGGAGCGGGGCAGGGCCCCGCCACCGCCTTCTTCCGCCGGCCCCGCCGCCGGCCA GCGCCACAGCCGGAGCGGGGCAGGGCCCCGCCGCCGCCTTCTTCCGCCGGCCCCGCCGCCGGCCA T C LPGAT1 Ensembl:ENSG00000123684 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:211830621..211830772 26863196 MeRIP-seq:(Medium) rs1301036579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340490,Human_RBP_ID_4073258 Human_Splice_Rec_185471,Human_Splice_Rec_185501 102821 RMVar_ID_102821 Human_SNP_ID_48611588 m1A Human chr1 - 212002531 212002531 212002531 ACATTCATGAGTGTGAGGTCAGTGTGACTGTTAATAGAGGAGATTAGTAGGAGGTGATGTTAGGT ACATTCATGAGTGTGAGGTCAGTGTGACTGTTCATAGAGGAGATTAGTAGGAGGTGATGTTAGGT T G INTS7 Ensembl:ENSG00000143493 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212002525..212002629 26863196 MeRIP-seq:(Medium) rs572277311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11195692 RMVar_hsa_circ_14223,RMVar_hsa_circ_139423,RMVar_hsa_circ_22215,RMVar_hsa_circ_69988,RMVar_hsa_circ_284011,RMVar_hsa_circ_48501,RMVar_hsa_circ_139419,RMVar_hsa_circ_372723,RMVar_hsa_circ_120963,RMVar_hsa_circ_368546,RMVar_hsa_circ_78479,RMVar_hsa_circ_139421,RMVar_hsa_circ_94667,RMVar_hsa_circ_139424,RMVar_hsa_circ_20687,RMVar_hsa_circ_332322,RMVar_hsa_circ_354209,RMVar_hsa_circ_139425 102822 RMVar_ID_102822 Human_SNP_ID_48619405 m1A Human chr1 - 212035475 212035475 212035475 GGGAAGATGGCGGTCCTGGGGTAGAGTTTGCAAGCTTTCTGACTAGGCTAGTCGAGTAACTATTC GGGAAGATGGCGGTCCTGGGGTAGAGTTTGCATGCTTTCTGACTAGGCTAGTCGAGTAACTATTC T A INTS7 Ensembl:ENSG00000143493 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:212035403..212035510 26863410 MeRIP-seq:(Medium) rs1324013134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340570,Human_RBP_ID_5485353,Human_RBP_ID_8297112,Human_RBP_ID_10754635,Human_RBP_ID_22350605,Human_RBP_ID_22431248,Human_RBP_ID_26315337,Human_RBP_ID_27799190 RMVar_hsa_circ_120963,RMVar_hsa_circ_78479,RMVar_hsa_circ_139421,RMVar_hsa_circ_139424 102823 RMVar_ID_102823 Human_SNP_ID_48619412 m1A Human chr1 + 212035491 212035491 212035491 AGCCTAGTCAGAAAGCTTGCAAACTCTACCCCAGGACCGCCATCTTCCCCCGCCGCCTTCTTGCT AGCCTAGTCAGAAAGCTTGCAAACTCTACCCCGGGACCGCCATCTTCCCCCGCCGCCTTCTTGCT A G lnc-DTL-4 RNACentral:URS00008C03D7 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:212035386..212035528;chr1:212035351..212035550;chr1:212035376..212035550 26863196 MeRIP-seq:(Medium) rs1161596556 Functional Loss SNV dbSNP153 33..33 33 - - - 102824 RMVar_ID_102824 Human_SNP_ID_48624630 m1A Human chr1 - 212055727 212055727 212055727 CAGGGGTGGGGTGATCCCCAGGCTTCCAGTGGAATGCTCAGGTAAGGGGCAGCAGCAGCTATGCT CAGGGGTGGGGTGATCCCCAGGCTTCCAGTGGGATGCTCAGGTAAGGGGCAGCAGCAGCTATGCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:212055682..212055814 26863196 MeRIP-seq:(Medium) rs1390186044 Functional Loss SNV dbSNP153 33..33 33 - - - 102825 RMVar_ID_102825 Human_SNP_ID_48631001 m1A Human chr1 - 212082416 212082416 212082416 CACTGTGAAATGTTATATTCCTATTTAAAAAAACCCCAGCAAACTTCAACCCTGCTTCTTTCTCC CACTGTGAAATGTTATATTCCTATTTAAAAAACCCCCAGCAAACTTCAACCCTGCTTCTTTCTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212082414..212082704 26863196 MeRIP-seq:(Medium) rs1041676268 Functional Loss SNV dbSNP153 33..33 33 - - - 102826 RMVar_ID_102826 Human_SNP_ID_48635223 m1A Human chr1 + 212100360 212100360 212100360 ATCCGCAGCTTGTGCCCCAAGCTGTGCTGGAGACCTCCCTCTTCCTTCAAATACTCCTACGTTCT ATCCGCAGCTTGTGCCCCAAGCTGTGCTGGAGCCCTCCCTCTTCCTTCAAATACTCCTACGTTCT A C DTL Ensembl:ENSG00000143476 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212100311..212100425 26863196 MeRIP-seq:(Medium) rs1260308657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5749913,Human_RBP_ID_8742453,Human_RBP_ID_17215464,Human_RBP_ID_17737683,Human_RBP_ID_18930398,Human_RBP_ID_22431251,Human_RBP_ID_26851823 Human_miRNA_ID_1969269,Human_miRNA_ID_2028088,Human_miRNA_ID_2688644,Human_miRNA_ID_2691807 RMVar_hsa_circ_106846,RMVar_hsa_circ_139431,RMVar_hsa_circ_139448,RMVar_hsa_circ_374928,RMVar_hsa_circ_376803,RMVar_hsa_circ_139449 102827 RMVar_ID_102827 Human_SNP_ID_48635297 m1A Human chr1 - 212100589 212100589 212100589 CAAGCCTCTGCTTGGGATGACTTCTGGCTCACAGGAATAAGGGCTTTTCTCGGAGACATGATCTT CAAGCCTCTGCTTGGGATGACTTCTGGCTCACCGGAATAAGGGCTTTTCTCGGAGACATGATCTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212100539..212100663 26863196 MeRIP-seq:(Medium) rs1167668791 Functional Loss SNV dbSNP153 33..33 33 - - - 102828 RMVar_ID_102828 Human_SNP_ID_48681291 m1A Human chr1 + 212295604 212295603 212295604 AGGAATACCAACATTGAGATAATGGGTAAGGGAAAAAGGTACAACCAAGAGCCAAGAGAGACAGC AGGAATACCAACATTGAGATAATGGGTAAGGG_AAAAGGTACAACCAAGAGCCAAGAGAGACAGC GA G PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212295598..212295859 26863196 MeRIP-seq:(Medium) rs1236643951 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23303152 102829 RMVar_ID_102829 Human_SNP_ID_48681292 m1A Human chr1 + 212295604 212295604 212295604 AGGAATACCAACATTGAGATAATGGGTAAGGGAAAAAGGTACAACCAAGAGCCAAGAGAGACAGC AGGAATACCAACATTGAGATAATGGGTAAGGGGAAAAGGTACAACCAAGAGCCAAGAGAGACAGC A G PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212295598..212295859 26863196 MeRIP-seq:(Medium) rs1461992642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303152 102830 RMVar_ID_102830 Human_SNP_ID_48681294 m1A Human chr1 + 212295606 212295606 212295606 GAATACCAACATTGAGATAATGGGTAAGGGAAAAAGGTACAACCAAGAGCCAAGAGAGACAGCTG GAATACCAACATTGAGATAATGGGTAAGGGAAGAAGGTACAACCAAGAGCCAAGAGAGACAGCTG A G PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212295604..212295827 26863196 MeRIP-seq:(Medium) rs1352074684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303152 102831 RMVar_ID_102831 Human_SNP_ID_48701335 m1A Human chr1 - 212377708 212377708 212377708 GACCTGGATCTTCCTTCTCCTTCCTTCCTCCAAGCCCAAACAGGGTAGGCTTCATGCAGGCCTGT GACCTGGATCTTCCTTCTCCTTCCTTCCTCCAGGCCCAAACAGGGTAGGCTTCATGCAGGCCTGT T C PACC1 Ensembl:ENSG00000065600 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:212377693..212385415 32194978 MeRIP-seq:(Medium) rs375158017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22634945 RMVar_hsa_circ_342311,RMVar_hsa_circ_367853,RMVar_hsa_circ_139467 102832 RMVar_ID_102832 Human_SNP_ID_48707940 m1A Human chr1 - 212404477 212404477 212404477 GGAGATGAGGTAGGAAAGATAGACTTGGTCAGATTATGGAGGGGTCTGAGTGTCAGGGTCTGTAC GGAGATGAGGTAGGAAAGATAGACTTGGTCAGGTTATGGAGGGGTCTGAGTGTCAGGGTCTGTAC T C PACC1 Ensembl:ENSG00000065600 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212404468..212404702 26863196 MeRIP-seq:(Medium) rs1218917315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10759145 102833 RMVar_ID_102833 Human_SNP_ID_48707957 m1A Human chr1 - 212404583 212404583 212404583 GGAGATGACATGAGCAACTGTATAGAGATGGGAATAAAATAGGACATGTCAGAGATCATGAATAG GGAGATGACATGAGCAACTGTATAGAGATGGGTATAAAATAGGACATGTCAGAGATCATGAATAG T A PACC1 Ensembl:ENSG00000065600 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212404548..212404681 26863196 MeRIP-seq:(Medium) rs188543708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10759146 102834 RMVar_ID_102834 Human_SNP_ID_48710448 m1A Human chr1 + 212414788 212414788 212414788 ATGGCACTGACCAGAGCTTCGGCACACCTGAGACCGCCCCAGCCCGCGGCGCACGGACGCAGCAC ATGGCACTGACCAGAGCTTCGGCACACCTGAGGCCGCCCCAGCCCGCGGCGCACGGACGCAGCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212414743..212414842 26863196 MeRIP-seq:(Medium) rs769102190 Functional Loss SNV dbSNP153 33..33 33 - - - 102835 RMVar_ID_102835 Human_SNP_ID_48710457 m1A Human chr1 + 212414796 212414796 212414796 GACCAGAGCTTCGGCACACCTGAGACCGCCCCAGCCCGCGGCGCACGGACGCAGCACTGCGGCCG GACCAGAGCTTCGGCACACCTGAGACCGCCCCCGCCCGCGGCGCACGGACGCAGCACTGCGGCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212414748..212414837 26863196 MeRIP-seq:(Medium) rs1350573652 Functional Loss SNV dbSNP153 33..33 33 - - - 102836 RMVar_ID_102836 Human_SNP_ID_48714030 m1A Human chr1 - 212431788 212431788 212431788 GAAGAGCACTTTGGTCAAAGGATCAGGTGCATAAATGCGGAGGAATGAGGATGCCCGGCTTGCTG GAAGAGCACTTTGGTCAAAGGATCAGGTGCATGAATGCGGAGGAATGAGGATGCCCGGCTTGCTG T C AC092803.3 Ensembl:ENSG00000287445 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212431744..212431822 26863196 MeRIP-seq:(Medium) rs564828627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_186006 102837 RMVar_ID_102837 Human_SNP_ID_48714335 m1A Human chr1 - 212433002 212432994 212433003 CCCGGGCTGTGGGCAGCCCCGGGGCCAGCGCCAGGACCAGGGCCAGCGCTGCCAGCGGCCGCAGC CCCGGGCTGTGGGCAGCCCCGGGGCCAGCGC_________GGCCAGCGCTGCCAGCGGCCGCAGC CCTGGTCCTG C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:212432876..212434770 26863410 MeRIP-seq:(Medium) rs1018412450 Functional Loss DEL dbSNP153 32..40 33 - - - 102838 RMVar_ID_102838 Human_SNP_ID_48714358 m1A Human chr1 + 212433072 212433072 212433072 CAGACACCGCGCCCTGCCGAGCGGGGGCCCCCAGTGCGGCTTTTCACCGAGGAGGAGCTGGCCCG CAGACACCGCGCCCTGCCGAGCGGGGGCCCCCTGTGCGGCTTTTCACCGAGGAGGAGCTGGCCCG A T NENF Ensembl:ENSG00000117691 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:212432976..212433075 32194978 MeRIP-seq:(Medium) rs1271946273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223798,Human_RBP_ID_340714,Human_RBP_ID_4022439,Human_RBP_ID_9319351,Human_RBP_ID_17737816 Human_Splice_Rec_186007,Human_Splice_Rec_186013,Human_Splice_Rec_186017,Human_Splice_Rec_186023 102839 RMVar_ID_102839 Human_SNP_ID_48714376 m1A Human chr1 + 212433116 212433116 212433116 CACCGAGGAGGAGCTGGCCCGCTATGGCGGGGAGGAGGTAGGCGGGGGTGTCGCGGGCCGAGGGA CACCGAGGAGGAGCTGGCCCGCTATGGCGGGGGGGAGGTAGGCGGGGGTGTCGCGGGCCGAGGGA A G NENF Ensembl:ENSG00000117691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:212432936..212434770;chr1:212432876..212433163;chr1:212432876..212433184;chr1:212432901..212433180 26863196 MeRIP-seq:(Medium) rs75793592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223798,Human_RBP_ID_340716,Human_RBP_ID_4073262,Human_RBP_ID_9320349,Human_RBP_ID_17647850,Human_RBP_ID_23361320 Human_Splice_Rec_186007,Human_Splice_Rec_186013,Human_Splice_Rec_186017,Human_Splice_Rec_186023 102840 RMVar_ID_102840 Human_SNP_ID_48717078 m1A Human chr1 - 212444421 212444421 212444421 ATCTGGCTCACAGTGTCATGGGTGAGGTCTGCAGGATCCAAGGACATCTTGGCTACCCCTCTAGT ATCTGGCTCACAGTGTCATGGGTGAGGTCTGCGGGATCCAAGGACATCTTGGCTACCCCTCTAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212444326..212445831 26863196 MeRIP-seq:(Medium) rs1297474008 Functional Loss SNV dbSNP153 33..33 33 - - - 102841 RMVar_ID_102841 Human_SNP_ID_48743926 m1A Human chr1 + 212558498 212558497 212558499 CGGCCCCGCCGACTGCTGACGCGGTGGCCCCAAGGGTCCAGGCCCGCACTTGCCCCACTCCCGCG CGGCCCCGCCGACTGCTGACGCGGTGGCCCCA__GGTCCAGGCCCGCACTTGCCCCACTCCCGCG AAG A lnc-ATF3-1,lnc-ATF3-1:2 RNACentral:URS0000D5BEE6,RNACentral:URS000000EAD5 lincRNA,lincRNA exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:212558446..212558663 26863196 MeRIP-seq:(Medium) rs757516664 Functional Loss DEL dbSNP153 33..34 33 - - - 102842 RMVar_ID_102842 Human_SNP_ID_48743940 m1A Human chr1 - 212558544 212558544 212558544 CAGGAGCTGGGCGCGGCCCTCGGGGACCGACTATGGGGGACGGCGCCGCGGGAGTGGGGCAAGTG CAGGAGCTGGGCGCGGCCCTCGGGGACCGACTGTGGGGGACGGCGCCGCGGGAGTGGGGCAAGTG T C AC092803.1 Ensembl:ENSG00000260805 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:212558282..212558834 26863196 MeRIP-seq:(Medium) rs891696178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17737836 102843 RMVar_ID_102843 Human_SNP_ID_48755653 m1A Human chr1 + 212608817 212608817 212608817 ACTGCACAGCTCTCTTCTCTCGCCGCCGCCCGAGCGCACCCTTCAGCCCGCGCGCCGGCCGTGAG ACTGCACAGCTCTCTTCTCTCGCCGCCGCCCGGGCGCACCCTTCAGCCCGCGCGCCGGCCGTGAG A G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:212608751..212609031;chr1:212608751..212609014;chr1:212608751..212609054;chr1:212608751..212609095 26863196 MeRIP-seq:(Medium) rs917959914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4022503,Human_RBP_ID_5413492,Human_RBP_ID_5456987,Human_RBP_ID_5485367,Human_RBP_ID_8297313,Human_RBP_ID_22024198,Human_RBP_ID_22782045 102844 RMVar_ID_102844 Human_SNP_ID_48755660 m1A Human chr1 - 212608826 212608826 212608826 CACCGAGGACTCACGGCCGGCGCGCGGGCTGAAGGGTGCGCTCGGGCGGCGGCGAGAGAAGAGAG CACCGAGGACTCACGGCCGGCGCGCGGGCTGACGGGTGCGCTCGGGCGGCGGCGAGAGAAGAGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212608776..212613482 26863196 MeRIP-seq:(Medium) rs1558237002 Functional Loss SNV dbSNP153 33..33 33 - - - 102845 RMVar_ID_102845 Human_SNP_ID_48755674 m1A Human chr1 + 212608877 212608877 212608877 GTGAGTCCTCGGTGCTCGCCCGCCGGCCAGACAAACAGCCCGCCCGACCCCGTCCCGACCCTGGC GTGAGTCCTCGGTGCTCGCCCGCCGGCCAGACCAACAGCCCGCCCGACCCCGTCCCGACCCTGGC A C ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:212608776..212608925 26863410 MeRIP-seq:(Medium) rs1016221009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224468,Human_RBP_ID_9319352,Human_RBP_ID_17338644 Human_Splice_Rec_186059,Human_Splice_Rec_186065,Human_Splice_Rec_186069,Human_Splice_Rec_186075 102846 RMVar_ID_102846 Human_SNP_ID_48755906 m1A Human chr1 + 212609422 212609422 212609422 GCAGAGAGGCACGAAGGCCGGAGGCTTGCGGGAGGGCTGCCCCACGCGCCGAGAGGAATGAATGG GCAGAGAGGCACGAAGGCCGGAGGCTTGCGGGGGGGCTGCCCCACGCGCCGAGAGGAATGAATGG A G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212609417..212609551 26863196 MeRIP-seq:(Medium) rs1350502599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224469,Human_RBP_ID_259065,Human_RBP_ID_3328788,Human_RBP_ID_5312829,Human_RBP_ID_17668099 102847 RMVar_ID_102847 Human_SNP_ID_48757058 m1A Human chr1 + 212614955 212614954 212614955 GTGGGGCTCTGGTGTTGGAGGTCTGGTGGGGGAGGGGGACTTGATCCCATGCCCCAGAGCCCCTG GTGGGGCTCTGGTGTTGGAGGTCTGGTGGGGG_GGGGGACTTGATCCCATGCCCCAGAGCCCCTG GA G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:212614948..212615125 26863410 MeRIP-seq:(Medium) rs1188115961 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_855785,Human_RBP_ID_22638046,Human_RBP_ID_26774692 Human_Splice_Rec_186077 102848 RMVar_ID_102848 Human_SNP_ID_48757059 m1A Human chr1 + 212614955 212614955 212614955 GTGGGGCTCTGGTGTTGGAGGTCTGGTGGGGGAGGGGGACTTGATCCCATGCCCCAGAGCCCCTG GTGGGGCTCTGGTGTTGGAGGTCTGGTGGGGGGGGGGGACTTGATCCCATGCCCCAGAGCCCCTG A G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:212614948..212615125 26863410 MeRIP-seq:(Medium) rs1178639115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_855785,Human_RBP_ID_22638046,Human_RBP_ID_26774692 Human_Splice_Rec_186077 102849 RMVar_ID_102849 Human_SNP_ID_48757102 m1A Human chr1 - 212615069 212615069 212615069 CCAGGAGGGGACAGGCAGGGGACGATGGCAGAAGCACTCACTTCCGAGGCAGAGACCTGGCCTGG CCAGGAGGGGACAGGCAGGGGACGATGGCAGAGGCACTCACTTCCGAGGCAGAGACCTGGCCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:212614974..212615100;chr1:212615001..212615100 26863196 MeRIP-seq:(Medium) rs1396768999 Functional Loss SNV dbSNP153 33..33 33 - - - 102850 RMVar_ID_102850 Human_SNP_ID_48757885 m1A Human chr1 + 212618183 212618183 212618183 AAAAAGAGGCGACGAGAAAGAAATAAGATTGCAGCTGCAAAGTGCCGAAACAAGAAGAAGGAGAA AAAAAGAGGCGACGAGAAAGAAATAAGATTGCTGCTGCAAAGTGCCGAAACAAGAAGAAGGAGAA A T ATF3 Ensembl:ENSG00000162772 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:212618126..212618200 26863196 MeRIP-seq:(Medium) rs113069548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25526,Human_RBP_ID_1420373,Human_RBP_ID_23361413,Human_RBP_ID_26312638,Human_RBP_ID_27801489 Human_Splice_Rec_186050,Human_Splice_Rec_186051,Human_Splice_Rec_186056,Human_Splice_Rec_186057,Human_Splice_Rec_186062,Human_Splice_Rec_186063,Human_Splice_Rec_186068,Human_Splice_Rec_186072,Human_Splice_Rec_186073,Human_Splice_Rec_186080,Human_Splice_Rec_186081,Human_Splice_Rec_186086,Human_Splice_Rec_186087,Human_Splice_Rec_186090,Human_Splice_Rec_186091,Human_Splice_Rec_186096,Human_Splice_Rec_186097,Human_Splice_Rec_186100,Human_Splice_Rec_186101 RMVar_hsa_circ_49934,RMVar_hsa_circ_362277 102851 RMVar_ID_102851 Human_SNP_ID_48776980 m1A Human chr1 - 212699837 212699837 212699837 CGTGGGTGCGGCACGAGGATGCCGGCGGCGGGACAGCGCCCGTAGGCAGCCCCACGGGCAGGGCG CGTGGGTGCGGCACGAGGATGCCGGCGGCGGGGCAGCGCCCGTAGGCAGCCCCACGGGCAGGGCG T C BATF3 Ensembl:ENSG00000123685 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212699501..212699985 26863196 MeRIP-seq:(Medium) rs1298914726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4022608 102852 RMVar_ID_102852 Human_SNP_ID_48777005 m1A Human chr1 - 212699892 212699892 212699892 CGCGTGGAGTAGCGGGGAGAGCGGGAAGCCTGAGGGGGCGGGGCCGGCGCGAGGCCGTGGGTGCG CGCGTGGAGTAGCGGGGAGAGCGGGAAGCCTGGGGGGGCGGGGCCGGCGCGAGGCCGTGGGTGCG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:212699791..212699959 26863196 MeRIP-seq:(Medium) rs1340690039 Functional Loss SNV dbSNP153 33..33 33 - - - 102853 RMVar_ID_102853 Human_SNP_ID_48782469 m1A Human chr1 - 212724257 212724226 212724257 TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGGAAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGA TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGG_______________________________GA CCCTCTCCCTCTCTCTCCACGGTCTCCCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212724225..212724308 26863196 MeRIP-seq:(Medium) rs1202347002 Functional Loss DEL dbSNP153 33..63 33 - - - 102854 RMVar_ID_102854 Human_SNP_ID_48782474 m1A Human chr1 - 212724257 212724232 212724257 TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGGAAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGA TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGG_________________________GAGAGGGA CCCTCTCTCTCCACGGTCTCCCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212724225..212724308 26863196 MeRIP-seq:(Medium) rs1338398760 Functional Loss DEL dbSNP153 33..57 33 - - - 102855 RMVar_ID_102855 Human_SNP_ID_48782488 m1A Human chr1 - 212724257 212724251 212724257 TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGGAAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGA TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGG______GAGACCGTGGAGAGAGAGGGAGAGGGA CCCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212724225..212724308 26863196 MeRIP-seq:(Medium) rs1259478418 Functional Loss DEL dbSNP153 33..38 33 - - - 102856 RMVar_ID_102856 Human_SNP_ID_48782489 m1A Human chr1 - 212724257 212724257 212724257 TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGGAAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGA TCAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGAGAGGGAGACCGTGGAGAGAGAGGGAGAGGGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:212724225..212724308 26863196 MeRIP-seq:(Medium) rs1282975119 Functional Loss SNV dbSNP153 33..33 33 - - - 102857 RMVar_ID_102857 Human_SNP_ID_48782591 m1A Human chr1 - 212724480 212724480 212724480 CACCTCGGGAGGCCGAGGTGGGCAGATCACTCACGGTCAGGAGCTGGAGACCAGCCCGGCCAACA CACCTCGGGAGGCCGAGGTGGGCAGATCACTCGCGGTCAGGAGCTGGAGACCAGCCCGGCCAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:212724428..212724578;chr1:212724426..212724526;chr1:212724409..212724587 26863196 MeRIP-seq:(Medium) rs1180460151 Functional Loss SNV dbSNP153 33..33 33 - - - 102858 RMVar_ID_102858 Human_SNP_ID_48784621 m1A Human chr1 - 212731887 212731887 212731887 GCCCTTATAGCTGCTGGGTCCTGGGGCAGGGTAGGGTGTCCCAGGACATGGAGCTGGAGCAGCCA GCCCTTATAGCTGCTGGGTCCTGGGGCAGGGTGGGGTGTCCCAGGACATGGAGCTGGAGCAGCCA T C NSL1 Ensembl:ENSG00000117697 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:212731845..212731939 26863196 MeRIP-seq:(Medium) rs1373212209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223799 102859 RMVar_ID_102859 Human_SNP_ID_48791091 m1A Human chr1 - 212760626 212760626 212760626 CGTCAGGCCCCCAGGCAGCAAGCACAGGCGGCAGTGGTGGTGGCAATGGACTGGGCTGGCCAGTC CGTCAGGCCCCCAGGCAGCAAGCACAGGCGGCCGTGGTGGTGGCAATGGACTGGGCTGGCCAGTC T G NSL1 Ensembl:ENSG00000117697 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212760577..212760716 26863196 MeRIP-seq:(Medium) rs1364386423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_800672,Human_RBP_ID_17099821 RMVar_hsa_circ_3992,RMVar_hsa_circ_343811,RMVar_hsa_circ_343931,RMVar_hsa_circ_139468 102860 RMVar_ID_102860 Human_SNP_ID_48799253 m1A Human chr1 - 212791534 212791534 212791534 GGAGATTCGGGAGCCCGCTCTGCGAGATGCGCAGTGGGTACGGGACCAGTTAGCCAGTTCTTTAC GGAGATTCGGGAGCCCGCTCTGCGAGATGCGCTGTGGGTACGGGACCAGTTAGCCAGTTCTTTAC T A NSL1 Ensembl:ENSG00000117697 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:212791526..212791750 32194978 MeRIP-seq:(Medium) rs750275587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340870,Human_RBP_ID_19035915 Human_Splice_Rec_186121,Human_Splice_Rec_186129,Human_Splice_Rec_186139,Human_Splice_Rec_186147,Human_Splice_Rec_186159,Human_Splice_Rec_186165 RMVar_hsa_circ_139471 102861 RMVar_ID_102861 Human_SNP_ID_48799254 m1A Human chr1 - 212791534 212791534 212791534 GGAGATTCGGGAGCCCGCTCTGCGAGATGCGCAGTGGGTACGGGACCAGTTAGCCAGTTCTTTAC GGAGATTCGGGAGCCCGCTCTGCGAGATGCGCCGTGGGTACGGGACCAGTTAGCCAGTTCTTTAC T G NSL1 Ensembl:ENSG00000117697 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:212791526..212791750 32194978 MeRIP-seq:(Medium) rs750275587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_340870,Human_RBP_ID_19035915 Human_Splice_Rec_186121,Human_Splice_Rec_186129,Human_Splice_Rec_186139,Human_Splice_Rec_186147,Human_Splice_Rec_186159,Human_Splice_Rec_186165 RMVar_hsa_circ_139471 102862 RMVar_ID_102862 Human_SNP_ID_48799355 m1A Human chr1 + 212791738 212791738 212791738 CCGCGAGCTCCTTGTCCCATGGAGGGTCAAGGACCACCAACTCAGGAGACCCCGCCATTTTTCGT CCGCGAGCTCCTTGTCCCATGGAGGGTCAAGGCCCACCAACTCAGGAGACCCCGCCATTTTTCGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212791601..212791775 26863196 MeRIP-seq:(Medium) rs1330635135 Functional Loss SNV dbSNP153 33..33 33 - - - 102863 RMVar_ID_102863 Human_SNP_ID_48815870 m1A Human chr1 - 212857999 212857999 212857999 GAGGCGGCCCCGCGGGTTGTGTTGCTGGAAAAAGGGGTCTCGATCCAGACCCCAAGAGAGGGTTC GAGGCGGCCCCGCGGGTTGTGTTGCTGGAAAACGGGGTCTCGATCCAGACCCCAAGAGAGGGTTC T G FLVCR1-DT Ensembl:ENSG00000198468 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212857948..212858075 26863196 MeRIP-seq:(Medium) rs892011621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_801344 102864 RMVar_ID_102864 Human_SNP_ID_48816013 m1A Human chr1 + 212858397 212858397 212858397 GGCCCCAGGAGGACCTCGGGCTGTGGGCCGGGAGAGCGGAGTCGGGGAGTGGGGCGGGGGAGCGA GGCCCCAGGAGGACCTCGGGCTGTGGGCCGGGGGAGCGGAGTCGGGGAGTGGGGCGGGGGAGCGA A G FLVCR1 Ensembl:ENSG00000162769 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212858251..212859004 26863196 MeRIP-seq:(Medium) rs927762933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_740963,Human_RBP_ID_4073263,Human_RBP_ID_5519342,Human_RBP_ID_8742490,Human_RBP_ID_8940204,Human_RBP_ID_9359824,Human_RBP_ID_9411381,Human_RBP_ID_18415710,Human_RBP_ID_18429421,Human_RBP_ID_22026127,Human_RBP_ID_22535657,Human_RBP_ID_22564886,Human_RBP_ID_22707199,Human_RBP_ID_26312640 102865 RMVar_ID_102865 Human_SNP_ID_48816034 m1A Human chr1 - 212858454 212858454 212858454 CCGCCGCCCCCTCCTCATCGTCTGGCCGCGCCATATCCCAGGCTCCCCGGCGCCACCTCGCTCCC CCGCCGCCCCCTCCTCATCGTCTGGCCGCGCCGTATCCCAGGCTCCCCGGCGCCACCTCGCTCCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:212858361..212858550 26863196 MeRIP-seq:(Medium) rs1468358104 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_639 GWAS_ID_13425 102866 RMVar_ID_102866 Human_SNP_ID_48816043 m1A Human chr1 - 212858470 212858470 212858470 GGGTGTCCGGGCGCCACCGCCGCCCCCTCCTCATCGTCTGGCCGCGCCATATCCCAGGCTCCCCG GGGTGTCCGGGCGCCACCGCCGCCCCCTCCTCTTCGTCTGGCCGCGCCATATCCCAGGCTCCCCG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:212858251..212858940 26863196 MeRIP-seq:(Medium) rs1029247819 Functional Loss SNV dbSNP153 33..33 33 - - - 102867 RMVar_ID_102867 Human_SNP_ID_48816044 m1A Human chr1 - 212858470 212858470 212858470 GGGTGTCCGGGCGCCACCGCCGCCCCCTCCTCATCGTCTGGCCGCGCCATATCCCAGGCTCCCCG GGGTGTCCGGGCGCCACCGCCGCCCCCTCCTCGTCGTCTGGCCGCGCCATATCCCAGGCTCCCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:212858251..212858940 26863196 MeRIP-seq:(Medium) rs1029247819 Functional Loss SNV dbSNP153 33..33 33 - - - 102868 RMVar_ID_102868 Human_SNP_ID_48839681 m1A Human chr1 - 212951362 212951362 212951362 ACCAAGGGGGAGCGGCGGCGGGAGCTCCGCGGAGGCTCCCTGCTTACCGGCGGTGCCTGAAATCA ACCAAGGGGGAGCGGCGGCGGGAGCTCCGCGGTGGCTCCCTGCTTACCGGCGGTGCCTGAAATCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212951333..212951490 26863196 MeRIP-seq:(Medium) rs1311258531 Functional Loss SNV dbSNP153 33..33 33 - - - 102869 RMVar_ID_102869 Human_SNP_ID_48839710 m1A Human chr1 + 212951469 212951469 212951469 GGGGCGCTGATCCCCTCGCCGCGCCCGCGCGCACACGCCCCCCGCCGCCGCCGCCGCTGCCGCCG GGGGCGCTGATCCCCTCGCCGCGCCCGCGCGCTCACGCCCCCCGCCGCCGCCGCCGCTGCCGCCG A T VASH2 Ensembl:ENSG00000143494 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212951418..212951547 26863196 MeRIP-seq:(Medium) rs1161178527 Functional Loss SNV dbSNP153 33..33 33 - - - 102870 RMVar_ID_102870 Human_SNP_ID_48855713 m1A Human chr1 + 213015700 213015700 213015700 CCATCTTCGCCCTCCGCGTGCGTCCAGTTCCCAGGCCCCGGGTTCCACCTCAATCTCTATAATCG CCATCTTCGCCCTCCGCGTGCGTCCAGTTCCCGGGCCCCGGGTTCCACCTCAATCTCTATAATCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:213015382..213015826;chr1:213015594..213015826 26863196 MeRIP-seq:(Medium) rs780269076 Functional Loss SNV dbSNP153 33..33 33 - - - 102871 RMVar_ID_102871 Human_SNP_ID_48864165 m1A Human chr1 + 213051362 213051361 213051363 AACCTGGACCGCGGCGGCGCCGGGTTTCCCTCATGATCCCGGGCGGGTGGCGGCGGCGGCAGAGG AACCTGGACCGCGGCGGCGCCGGGTTTCCCTC__GATCCCGGGCGGGTGGCGGCGGCGGCAGAGG CAT C RPS6KC1 Ensembl:ENSG00000136643 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:213051311..213051483 26863196 MeRIP-seq:(Medium) rs749462285 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_223990,Human_RBP_ID_4074748,Human_RBP_ID_9359828,Human_RBP_ID_17738094,Human_RBP_ID_22871481,Human_RBP_ID_26312642 102872 RMVar_ID_102872 Human_SNP_ID_48864268 m1A Human chr1 - 213051534 213051534 213051534 ACCCCAGATCCTCAGGTCCCAATCCAAGCTCTACCCCAGCCCGACACCGGCACTCACCCGGGCGG ACCCCAGATCCTCAGGTCCCAATCCAAGCTCTGCCCCAGCCCGACACCGGCACTCACCCGGGCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:213051527..213051647 26863196 MeRIP-seq:(Medium) rs760028554 Functional Loss SNV dbSNP153 33..33 33 - - - 102873 RMVar_ID_102873 Human_SNP_ID_48889255 m1A Human chr1 + 213153259 213153259 213153259 GGGAGAGGGAGACCGTGGGGAGAGGGAGAGGGAGAGGGAGAGGGAGAGGCAAAGGCAGGCGCAGA GGGAGAGGGAGACCGTGGGGAGAGGGAGAGGGCGAGGGAGAGGGAGAGGCAAAGGCAGGCGCAGA A C RPS6KC1 Ensembl:ENSG00000136643 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:213153215..213153298 26863196 MeRIP-seq:(Medium) rs1365206368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204,RMVar_hsa_circ_335761,RMVar_hsa_circ_350671,RMVar_hsa_circ_304783,RMVar_hsa_circ_307846,RMVar_hsa_circ_302070,RMVar_hsa_circ_277202,RMVar_hsa_circ_321291,RMVar_hsa_circ_53265,RMVar_hsa_circ_329114,RMVar_hsa_circ_44685,RMVar_hsa_circ_15956,RMVar_hsa_circ_297970,RMVar_hsa_circ_281529,RMVar_hsa_circ_11029,RMVar_hsa_circ_304547,RMVar_hsa_circ_139520,RMVar_hsa_circ_345029,RMVar_hsa_circ_31995,RMVar_hsa_circ_347368,RMVar_hsa_circ_308848,RMVar_hsa_circ_273353,RMVar_hsa_circ_285673,RMVar_hsa_circ_97583,RMVar_hsa_circ_139521,RMVar_hsa_circ_139522,RMVar_hsa_circ_139523 102874 RMVar_ID_102874 Human_SNP_ID_48915714 m1A Human chr1 + 213263976 213263975 213263976 AGAATAGTCTTGGTGGAATGAATGGTTTGAACAAAGGCAAGGAAGGAGTCTGAAAGACCCAAGTT AGAATAGTCTTGGTGGAATGAATGGTTTGAAC_AAGGCAAGGAAGGAGTCTGAAAGACCCAAGTT CA C RPS6KC1 Ensembl:ENSG00000136643 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:213263878..213264071 26863196 MeRIP-seq:(Medium) rs961948956 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22520466 RMVar_hsa_circ_97583,RMVar_hsa_circ_139521 102875 RMVar_ID_102875 Human_SNP_ID_49155052 m1A Human chr1 + 214281252 214281249 214281252 TCGGGCACAGCCGGCGGCCGCGCCCCGCCGCCACCATGAGGGCCGAGGGCCTCGGCGGCCTGGAG TCGGGCACAGCCGGCGGCCGCGCCCCGCCG___CCATGAGGGCCGAGGGCCTCGGCGGCCTGGAG GCCA G SMYD2 Ensembl:ENSG00000143499 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:214281171..214281291 26863196 MeRIP-seq:(Medium) rs1413867562 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4073267 102876 RMVar_ID_102876 Human_SNP_ID_49155073 m1A Human chr1 - 214281288 214281287 214281288 CCGCAGCCCCCGGCCTTTGCCCGGGCTGCAGAAGCGCTCCAGGCCGCCGAGGCCCTCGGCCCTCA CCGCAGCCCCCGGCCTTTGCCCGGGCTGCAGA_GCGCTCCAGGCCGCCGAGGCCCTCGGCCCTCA CT C lnc-PTPN14-2,lnc-PTPN14-2:2,lnc-PTPN14-2:3,lnc-PTPN14-2:4 RNACentral:URS0000D57614,RNACentral:URS0000D5A70B,RNACentral:URS0000D5AE24,RNACentral:URS0000D56E09 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:214281201..214281302 32194978 MeRIP-seq:(Medium) rs777545747 Functional Loss DEL dbSNP153 33..33 33 - - - 102877 RMVar_ID_102877 Human_SNP_ID_49177958 m1A Human chr1 - 214378035 214378035 214378035 ACAGAAGAGGCCGCTGATGTTGGCAGCATTGAATGGGCTCTCGGTGGCTCGAGTCTCAGGGCGGG ACAGAAGAGGCCGCTGATGTTGGCAGCATTGAGTGGGCTCTCGGTGGCTCGAGTCTCAGGGCGGG T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:214377926..214378054;chr1:214377915..214378075 26863196 MeRIP-seq:(Medium) rs751417115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21688,Human_RBP_ID_8742701 Human_Splice_Rec_187336,Human_Splice_Rec_187337,Human_Splice_Rec_187370,Human_Splice_Rec_187371 RMVar_hsa_circ_4187,RMVar_hsa_circ_299257,RMVar_hsa_circ_346017,RMVar_hsa_circ_139558,RMVar_hsa_circ_349906,RMVar_hsa_circ_82860,RMVar_hsa_circ_334363,RMVar_hsa_circ_139559,RMVar_hsa_circ_87360,RMVar_hsa_circ_92930,RMVar_hsa_circ_85229,RMVar_hsa_circ_139560,RMVar_hsa_circ_139561,RMVar_hsa_circ_139562 102878 RMVar_ID_102878 Human_SNP_ID_49177959 m1A Human chr1 - 214378035 214378035 214378035 ACAGAAGAGGCCGCTGATGTTGGCAGCATTGAATGGGCTCTCGGTGGCTCGAGTCTCAGGGCGGG ACAGAAGAGGCCGCTGATGTTGGCAGCATTGACTGGGCTCTCGGTGGCTCGAGTCTCAGGGCGGG T G PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:214377926..214378054;chr1:214377915..214378075 26863196 MeRIP-seq:(Medium) rs751417115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21688,Human_RBP_ID_8742701 Human_Splice_Rec_187336,Human_Splice_Rec_187337,Human_Splice_Rec_187370,Human_Splice_Rec_187371 RMVar_hsa_circ_4187,RMVar_hsa_circ_299257,RMVar_hsa_circ_346017,RMVar_hsa_circ_139558,RMVar_hsa_circ_349906,RMVar_hsa_circ_82860,RMVar_hsa_circ_334363,RMVar_hsa_circ_139559,RMVar_hsa_circ_87360,RMVar_hsa_circ_92930,RMVar_hsa_circ_85229,RMVar_hsa_circ_139560,RMVar_hsa_circ_139561,RMVar_hsa_circ_139562 102879 RMVar_ID_102879 Human_SNP_ID_49179331 m1A Human chr1 - 214383850 214383850 214383850 TCAAGTCGCTCCACCTCCCCATGGCTCGCCGCAACACGCTCCGGGAGCAGGGACCGCCCGAGGAG TCAAGTCGCTCCACCTCCCCATGGCTCGCCGCGACACGCTCCGGGAGCAGGGACCGCCCGAGGAG T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:214383801..214384000 26863196 MeRIP-seq:(Medium) rs1278538933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24634351 RMVar_hsa_circ_349906,RMVar_hsa_circ_82860,RMVar_hsa_circ_334363,RMVar_hsa_circ_139559,RMVar_hsa_circ_87360,RMVar_hsa_circ_83741,RMVar_hsa_circ_85229,RMVar_hsa_circ_139560,RMVar_hsa_circ_139561,RMVar_hsa_circ_333678,RMVar_hsa_circ_369866,RMVar_hsa_circ_266872,RMVar_hsa_circ_139564,RMVar_hsa_circ_139565,RMVar_hsa_circ_139563 102880 RMVar_ID_102880 Human_SNP_ID_49179642 m1A Human chr1 - 214384552 214384552 214384552 ACTACATCCCGAGCCACCGGCACAGCGCGATCATCGTGCCCTCGTACAGGCCAACCCCCGATTAT ACTACATCCCGAGCCACCGGCACAGCGCGATCGTCGTGCCCTCGTACAGGCCAACCCCCGATTAT T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:214384505..214384645 26863196 MeRIP-seq:(Medium) rs1341505880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26852163 Human_miRNA_ID_2717022 RMVar_hsa_circ_349906,RMVar_hsa_circ_82860,RMVar_hsa_circ_334363,RMVar_hsa_circ_139559,RMVar_hsa_circ_87360,RMVar_hsa_circ_83741,RMVar_hsa_circ_85229,RMVar_hsa_circ_139560,RMVar_hsa_circ_139561,RMVar_hsa_circ_333678,RMVar_hsa_circ_369866,RMVar_hsa_circ_266872,RMVar_hsa_circ_139564,RMVar_hsa_circ_139565,RMVar_hsa_circ_139563 102881 RMVar_ID_102881 Human_SNP_ID_49181244 m1A Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGTTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T A PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:214390976..214391050 26863196 MeRIP-seq:(Medium) rs7550799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222385,Human_RBP_ID_17224160,Human_RBP_ID_19035924 Human_Splice_Rec_187330,Human_Splice_Rec_187331,Human_Splice_Rec_187364,Human_Splice_Rec_187365 GWAS_ID_5113 RMVar_hsa_circ_28179,RMVar_hsa_circ_83741,RMVar_hsa_circ_369866,RMVar_hsa_circ_266872,RMVar_hsa_circ_89481,RMVar_hsa_circ_102502,RMVar_hsa_circ_139564,RMVar_hsa_circ_139565,RMVar_hsa_circ_99604,RMVar_hsa_circ_101562,RMVar_hsa_circ_139567,RMVar_hsa_circ_139568,RMVar_hsa_circ_369918,RMVar_hsa_circ_139566,RMVar_hsa_circ_284728,RMVar_hsa_circ_92743,RMVar_hsa_circ_139570,RMVar_hsa_circ_139571,RMVar_hsa_circ_139572,RMVar_hsa_circ_139569 102882 RMVar_ID_102882 Human_SNP_ID_49181245 m1A Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGGTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:214390976..214391050 26863196 MeRIP-seq:(Medium) rs7550799 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_222385,Human_RBP_ID_17224160,Human_RBP_ID_19035924 Human_Splice_Rec_187330,Human_Splice_Rec_187331,Human_Splice_Rec_187364,Human_Splice_Rec_187365 GWAS_ID_5113 RMVar_hsa_circ_28179,RMVar_hsa_circ_83741,RMVar_hsa_circ_369866,RMVar_hsa_circ_266872,RMVar_hsa_circ_89481,RMVar_hsa_circ_102502,RMVar_hsa_circ_139564,RMVar_hsa_circ_139565,RMVar_hsa_circ_99604,RMVar_hsa_circ_101562,RMVar_hsa_circ_139567,RMVar_hsa_circ_139568,RMVar_hsa_circ_369918,RMVar_hsa_circ_139566,RMVar_hsa_circ_284728,RMVar_hsa_circ_92743,RMVar_hsa_circ_139570,RMVar_hsa_circ_139571,RMVar_hsa_circ_139572,RMVar_hsa_circ_139569 102883 RMVar_ID_102883 Human_SNP_ID_49185011 m1A Human chr1 + 214405201 214405201 214405201 CCTTACGTCCTGTCTCAGCTACCACTTCCCTCAATAGGGCTCTCCTCTCTCCCCAGCTGGACGTA CCTTACGTCCTGTCTCAGCTACCACTTCCCTCGATAGGGCTCTCCTCTCTCCCCAGCTGGACGTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:214405151..214405325 26863196 MeRIP-seq:(Medium) rs61819560 Functional Loss SNV dbSNP153 33..33 33 - - - 102884 RMVar_ID_102884 Human_SNP_ID_49185012 m1A Human chr1 + 214405201 214405201 214405201 CCTTACGTCCTGTCTCAGCTACCACTTCCCTCAATAGGGCTCTCCTCTCTCCCCAGCTGGACGTA CCTTACGTCCTGTCTCAGCTACCACTTCCCTCTATAGGGCTCTCCTCTCTCCCCAGCTGGACGTA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:214405151..214405325 26863196 MeRIP-seq:(Medium) rs61819560 Functional Loss SNV dbSNP153 33..33 33 - - - 102885 RMVar_ID_102885 Human_SNP_ID_49188831 m1A Human chr1 - 214421726 214421726 214421726 GGGGAGCACCGCACACTTACGACAGCTCAGGTATGGGGTGTGTGGTGAGATATGAAGTTGGAAAA GGGGAGCACCGCACACTTACGACAGCTCAGGTGTGGGGTGTGTGGTGAGATATGAAGTTGGAAAA T C PTPN14 Ensembl:ENSG00000152104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:214421718..214421914 26863196 MeRIP-seq:(Medium) rs1302014521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28179,RMVar_hsa_circ_266872,RMVar_hsa_circ_102502,RMVar_hsa_circ_139568,RMVar_hsa_circ_93998,RMVar_hsa_circ_324235,RMVar_hsa_circ_347988,RMVar_hsa_circ_139573,RMVar_hsa_circ_347339 102886 RMVar_ID_102886 Human_SNP_ID_49233155 m1A Human chr1 + 214603276 214603276 214603276 GACTCTGGGCTCCAGCCCGCCGAAGCCGCGCCAGAACTGTACTCTCCGAGAGGTCGTTTTCCCGT GACTCTGGGCTCCAGCCCGCCGAAGCCGCGCCGGAACTGTACTCTCCGAGAGGTCGTTTTCCCGT A G CENPF Ensembl:ENSG00000117724 Protein coding exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:214603226..214603421;chr1:214603226..214603371;chr1:214603226..214603381 26863196 MeRIP-seq:(Medium) rs956092032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223813,Human_RBP_ID_341307,Human_RBP_ID_4023413,Human_RBP_ID_8742740,Human_RBP_ID_9270585,Human_RBP_ID_10767836,Human_RBP_ID_18562342,Human_RBP_ID_26312645,Human_RBP_ID_27801505 Human_Splice_Rec_187391,Human_Splice_Rec_187395 102887 RMVar_ID_102887 Human_SNP_ID_49242391 m1A Human chr1 - 214640436 214640436 214640436 TGAGAACTCAGCTTTCTGCTGTAGCTCCATATAAGCTAGTTTCTGGGTCTCTACCTCCACTGACT TGAGAACTCAGCTTTCTGCTGTAGCTCCATATTAGCTAGTTTCTGGGTCTCTACCTCCACTGACT T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:214640352..214640442 26863410 MeRIP-seq:(Medium) rs1176796815 Functional Loss SNV dbSNP153 33..33 33 - - - 102888 RMVar_ID_102888 Human_SNP_ID_49244209 m1A Human chr1 + 214646001 214646001 214646001 GAAGCAGCTGCACATCGCAGAGAAACTGAAAGAACGCGAGCGGGAGAATGATTCACTTAAGGATA GAAGCAGCTGCACATCGCAGAGAAACTGAAAGGACGCGAGCGGGAGAATGATTCACTTAAGGATA A G CENPF Ensembl:ENSG00000117724 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:214645951..214646050 32194978 MeRIP-seq:(Medium) rs777492814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18914,Human_RBP_ID_8742910,Human_RBP_ID_10769094 Human_miRNA_ID_1181051,Human_miRNA_ID_2564465 RMVar_hsa_circ_111638,RMVar_hsa_circ_139579,RMVar_hsa_circ_61798,RMVar_hsa_circ_265901 102889 RMVar_ID_102889 Human_SNP_ID_49245021 m1A Human chr1 + 214648745 214648745 214648745 GGAAATGCATGAGATGGCACAGAAAACAGCAGAGCTGCAAGAAGAACTCAGTGGAGAGAAAAATA GGAAATGCATGAGATGGCACAGAAAACAGCAGGGCTGCAAGAAGAACTCAGTGGAGAGAAAAATA A G CENPF Ensembl:ENSG00000117724 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:214648696..214648857 26863196 MeRIP-seq:(Medium) rs1558188363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18922,Human_RBP_ID_4023775,Human_RBP_ID_5754382,Human_RBP_ID_8742948,Human_RBP_ID_10769213,Human_RBP_ID_22486962 Human_Splice_Rec_187420,Human_Splice_Rec_187421,Human_Splice_Rec_187435,Human_Splice_Rec_187441 Human_miRNA_ID_2011278,Human_miRNA_ID_2394301,Human_miRNA_ID_2757633 RMVar_hsa_circ_111638,RMVar_hsa_circ_139579,RMVar_hsa_circ_61798,RMVar_hsa_circ_265901,RMVar_hsa_circ_11417,RMVar_hsa_circ_357250 102890 RMVar_ID_102890 Human_SNP_ID_49245034 m1A Human chr1 + 214648777 214648777 214648777 AGCTGCAAGAAGAACTCAGTGGAGAGAAAAATAGGCTAGCTGGAGAGTTGCAGTTACTGTTGGAA AGCTGCAAGAAGAACTCAGTGGAGAGAAAAATGGGCTAGCTGGAGAGTTGCAGTTACTGTTGGAA A G CENPF Ensembl:ENSG00000117724 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:214648676..214648870 26863196 MeRIP-seq:(Medium) rs1189685423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18922,Human_RBP_ID_341338,Human_RBP_ID_1151932,Human_RBP_ID_1735937,Human_RBP_ID_4023777,Human_RBP_ID_5754383,Human_RBP_ID_8742949,Human_RBP_ID_9485845,Human_RBP_ID_10769216,Human_RBP_ID_17061661,Human_RBP_ID_22873673 Human_Splice_Rec_187421,Human_Splice_Rec_187435,Human_Splice_Rec_187441 RMVar_hsa_circ_111638,RMVar_hsa_circ_139579,RMVar_hsa_circ_61798,RMVar_hsa_circ_265901,RMVar_hsa_circ_11417,RMVar_hsa_circ_357250 102891 RMVar_ID_102891 Human_SNP_ID_49245043 m1A Human chr1 - 214648798 214648798 214648798 TACTTTGCTGCTCTTTATTTCTTCCAACAGTAACTGCAACTCTCCAGCTAGCCTATTTTTCTCTC TACTTTGCTGCTCTTTATTTCTTCCAACAGTACCTGCAACTCTCCAGCTAGCCTATTTTTCTCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:214648701..214651825 26863196 MeRIP-seq:(Medium) rs773633110 Functional Loss SNV dbSNP153 33..33 33 - - - 102892 RMVar_ID_102892 Human_SNP_ID_49248839 m1A Human chr1 + 214663666 214663666 214663666 TCCGAGAACCCACCACGAAATCCGTCCCAGTCAATAATCTTCCTGAGAGAAGTCCGACTGACAGC TCCGAGAACCCACCACGAAATCCGTCCCAGTCGATAATCTTCCTGAGAGAAGTCCGACTGACAGC A G CENPF Ensembl:ENSG00000117724 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:214663576..214663675 32194978 MeRIP-seq:(Medium) rs202111915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18935,Human_RBP_ID_341345,Human_RBP_ID_974879,Human_RBP_ID_1735964,Human_RBP_ID_2122085,Human_RBP_ID_4088797,Human_RBP_ID_5754485,Human_RBP_ID_8742987,Human_RBP_ID_10769584,Human_RBP_ID_17215640,Human_RBP_ID_17333173,Human_RBP_ID_17449683,Human_RBP_ID_17738536,Human_RBP_ID_18562503,Human_RBP_ID_22134966,Human_RBP_ID_22782081,Human_RBP_ID_26852409,Human_RBP_ID_27175237,Human_RBP_ID_27393807,Human_RBP_ID_27586804 Human_Splice_Rec_187432 Human_miRNA_ID_3115797 RMVar_hsa_circ_139581,RMVar_hsa_circ_86290 102893 RMVar_ID_102893 Human_SNP_ID_49463106 m1A Human chr1 + 215567413 215567410 215567413 GCTGCGGCGGCGTCGGTGGCAGCGGAGCACGGAGAAGAGGCCCGGGCGGCCCGGCGGCCTGGAGG GCTGCGGCGGCGTCGGTGGCAGCGGAGCAC___GAAGAGGCCCGGGCGGCCCGGCGGCCTGGAGG CGGA C KCTD3 Ensembl:ENSG00000136636 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:215567293..215567775 26863196 MeRIP-seq:(Medium) rs1432508813 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4073269,Human_RBP_ID_18969596,Human_RBP_ID_22871485,Human_RBP_ID_23117686 102894 RMVar_ID_102894 Human_SNP_ID_49463110 m1A Human chr1 + 215567415 215567415 215567415 TGCGGCGGCGTCGGTGGCAGCGGAGCACGGAGAAGAGGCCCGGGCGGCCCGGCGGCCTGGAGGCC TGCGGCGGCGTCGGTGGCAGCGGAGCACGGAGGAGAGGCCCGGGCGGCCCGGCGGCCTGGAGGCC A G KCTD3 Ensembl:ENSG00000136636 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:215567243..215567952 26863196 MeRIP-seq:(Medium) rs1197734222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4024071,Human_RBP_ID_9271757,Human_RBP_ID_18969596,Human_RBP_ID_22871485,Human_RBP_ID_23117686 102895 RMVar_ID_102895 Human_SNP_ID_49463112 m1A Human chr1 + 215567418 215567418 215567418 GGCGGCGTCGGTGGCAGCGGAGCACGGAGAAGAGGCCCGGGCGGCCCGGCGGCCTGGAGGCCGCG GGCGGCGTCGGTGGCAGCGGAGCACGGAGAAGGGGCCCGGGCGGCCCGGCGGCCTGGAGGCCGCG A G KCTD3 Ensembl:ENSG00000136636 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:215567301..215574090 26863196 MeRIP-seq:(Medium) rs760117391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4073269,Human_RBP_ID_9271757,Human_RBP_ID_18969596,Human_RBP_ID_22871485,Human_RBP_ID_23117686 102896 RMVar_ID_102896 Human_SNP_ID_49475735 m1A Human chr1 - 215620531 215620531 215620531 GTAGTCTTTGTAGGAGATGGGGACGCAGTACCAGGTGAGTCAGTTCCTCCATCGGAAGTACTTGG GTAGTCTTTGTAGGAGATGGGGACGCAGTACCGGGTGAGTCAGTTCCTCCATCGGAAGTACTTGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:215620426..215620575 26863196 MeRIP-seq:(Medium) rs770452831 Functional Loss SNV dbSNP153 33..33 33 - - - 102897 RMVar_ID_102897 Human_SNP_ID_49475790 m1A Human chr1 + 215620635 215620635 215620635 GGAGTACAGCTTGTGAAAACTCACCAAAATGAATAGTTGTTTCGTTACATTTAGATGAAAGTTAA GGAGTACAGCTTGTGAAAACTCACCAAAATGACTAGTTGTTTCGTTACATTTAGATGAAAGTTAA A C KCTD3 Ensembl:ENSG00000136636 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:215620601..215620650 26863196 MeRIP-seq:(Medium) rs766740712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1420825,Human_RBP_ID_17738718 102898 RMVar_ID_102898 Human_SNP_ID_49934227 m1A Human chr1 - 217430782 217430782 217430782 GCAATGCCCAGACAAACGTGAGCACACCCACCAGTTTCTAAAATGGAATAGACAGGAAAAGATTG GCAATGCCCAGACAAACGTGAGCACACCCACCGGTTTCTAAAATGGAATAGACAGGAAAAGATTG T C GPATCH2 Ensembl:ENSG00000092978 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs166449 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13426 102899 RMVar_ID_102899 Human_SNP_ID_49956312 m1A Human chr1 + 217524903 217524900 217524903 GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGAGAGGGGGGAGGGGGGAGGGGGGAGGGG___GGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:217524800..217524950;chr1:217524790..217524926 26863196 MeRIP-seq:(Medium) rs1558458181 Functional Loss DEL dbSNP153 31..33 33 - - - 102900 RMVar_ID_102900 Human_SNP_ID_49956315 m1A Human chr1 + 217524903 217524901 217524903 GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGG__GGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:217524800..217524950;chr1:217524790..217524926 26863196 MeRIP-seq:(Medium) rs1558458190 Functional Loss DEL dbSNP153 32..33 33 - - - 102901 RMVar_ID_102901 Human_SNP_ID_49956318 m1A Human chr1 + 217524903 217524902 217524903 GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGG_GGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:217524800..217524950;chr1:217524790..217524926 26863196 MeRIP-seq:(Medium) rs1558458210 Functional Loss DEL dbSNP153 33..33 33 - - - 102902 RMVar_ID_102902 Human_SNP_ID_49956321 m1A Human chr1 + 217524903 217524903 217524903 GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG GGAGAGGGGGGAGGGGGGAGGGGGGAGGGGGGGGGGGGGAGGGGGAGGGGGGAGAGGGGAGAGGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:217524800..217524950;chr1:217524790..217524926 26863196 MeRIP-seq:(Medium) rs1330150659 Functional Loss SNV dbSNP153 33..33 33 - - - 102903 RMVar_ID_102903 Human_SNP_ID_49975416 m1A Human chr1 - 217606244 217606244 217606244 ACTGCTCTAAACTCTTCTCCTGACCACAGAGCACATAGGCCTTCTCCCTCCATCATTTAAGCTAA ACTGCTCTAAACTCTTCTCCTGACCACAGAGCGCATAGGCCTTCTCCCTCCATCATTTAAGCTAA T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:217606165..217606299 26863410 MeRIP-seq:(Medium) rs970481446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110936,RMVar_hsa_circ_76851,RMVar_hsa_circ_139613,RMVar_hsa_circ_119353,RMVar_hsa_circ_139614,RMVar_hsa_circ_139615 102904 RMVar_ID_102904 Human_SNP_ID_50143006 m1A Human chr1 - 218285363 218285363 218285363 CCATTTTCATCTTCTTCTTTGGGGTCTTTTTCAGGTTTTCTTCCTCACTCACACGTGAGTCCGGA CCATTTTCATCTTCTTCTTTGGGGTCTTTTTCGGGTTTTCTTCCTCACTCACACGTGAGTCCGGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:218285301..218302402 26863196 MeRIP-seq:(Medium) rs1269824308 Functional Loss SNV dbSNP153 33..33 33 - - - 102905 RMVar_ID_102905 Human_SNP_ID_50146819 m1A Human chr1 - 218302258 218302258 218302258 TAGAACCAAAGAGTAAAGGCAAATTAAACTTTAATATCCTAGGCAGAGGCTGCCAAGGCCCCCCG TAGAACCAAAGAGTAAAGGCAAATTAAACTTTGATATCCTAGGCAGAGGCTGCCAAGGCCCCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:218302255..218302389 26863196 MeRIP-seq:(Medium) rs1362468676 Functional Loss SNV dbSNP153 33..33 33 - - - 102906 RMVar_ID_102906 Human_SNP_ID_50148025 m1A Human chr1 + 218307484 218307484 218307484 TGCTGTTCAGAAACATCAAAAGAATGTTGATGAAAAGGTTAAGGAAGCTGGAAGTTCTATGAGAA TGCTGTTCAGAAACATCAAAAGAATGTTGATGTAAAGGTTAAGGAAGCTGGAAGTTCTATGAGAA A T RRP15 Ensembl:ENSG00000067533 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:218304969..218307484 26863196 MeRIP-seq:(Medium) rs767191713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1736296,Human_RBP_ID_23364031 Human_Splice_Rec_188368 RMVar_hsa_circ_56431,RMVar_hsa_circ_267245,RMVar_hsa_circ_86346,RMVar_hsa_circ_139620,RMVar_hsa_circ_139621,RMVar_hsa_circ_76568 102907 RMVar_ID_102907 Human_SNP_ID_50359183 m1A Human chr1 + 219173945 219173945 219173945 TTCTGCAGCGCTGTATCGTGTCGCCGGCAGGGAGGCATAGCGCCTCTCTGATCTTCCTGCATGGC TTCTGCAGCGCTGTATCGTGTCGCCGGCAGGGGGGCATAGCGCCTCTCTGATCTTCCTGCATGGC A G LYPLAL1 Ensembl:ENSG00000143353 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:219173909..219174024 26863196 MeRIP-seq:(Medium) rs1553295292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224070,Human_RBP_ID_4074753,Human_RBP_ID_9319360,Human_RBP_ID_22427785,Human_RBP_ID_23364230 Human_Splice_Rec_188527,Human_Splice_Rec_188533,Human_Splice_Rec_188541,Human_Splice_Rec_188547,Human_Splice_Rec_188555,Human_Splice_Rec_188563,Human_Splice_Rec_188581 102908 RMVar_ID_102908 Human_SNP_ID_50359194 m1A Human chr1 - 219173959 219173959 219173959 TGAAATCCACCTGAGCCATGCAGGAAGATCAGAGAGGCGCTATGCCTCCCTGCCGGCGACACGAT TGAAATCCACCTGAGCCATGCAGGAAGATCAGTGAGGCGCTATGCCTCCCTGCCGGCGACACGAT T A LYPLAL1-DT Ensembl:ENSG00000228063 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:219173908..219174036 26863196 MeRIP-seq:(Medium) rs776192937 Functional Loss SNV dbSNP153 33..33 33 - - - 102909 RMVar_ID_102909 Human_SNP_ID_50359200 m1A Human chr1 - 219173970 219173970 219173970 GGACGTAAAATTGAAATCCACCTGAGCCATGCAGGAAGATCAGAGAGGCGCTATGCCTCCCTGCC GGACGTAAAATTGAAATCCACCTGAGCCATGCGGGAAGATCAGAGAGGCGCTATGCCTCCCTGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:219173942..219174091 26863410 MeRIP-seq:(Medium) rs1234665347 Functional Loss SNV dbSNP153 33..33 33 - - - 102910 RMVar_ID_102910 Human_SNP_ID_50359201 m1A Human chr1 - 219173970 219173970 219173970 GGACGTAAAATTGAAATCCACCTGAGCCATGCAGGAAGATCAGAGAGGCGCTATGCCTCCCTGCC GGACGTAAAATTGAAATCCACCTGAGCCATGCCGGAAGATCAGAGAGGCGCTATGCCTCCCTGCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:219173942..219174091 26863410 MeRIP-seq:(Medium) rs1234665347 Functional Loss SNV dbSNP153 33..33 33 - - - 102911 RMVar_ID_102911 Human_SNP_ID_50360434 m1A Human chr1 + 219179198 219179198 219179198 AAGAATGTGGATCAAGCAGGTTTTAAATCAAGATTTAACATTCCAACACATAAAAATTATTTATC AAGAATGTGGATCAAGCAGGTTTTAAATCAAGGTTTAACATTCCAACACATAAAAATTATTTATC A G LYPLAL1 Ensembl:ENSG00000143353 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:219179098..219179203 26863196 MeRIP-seq:(Medium) rs1165605765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1736346,Human_RBP_ID_9359850,Human_RBP_ID_17215705,Human_RBP_ID_17449772,Human_RBP_ID_18522916,Human_RBP_ID_21909690,Human_RBP_ID_22135162,Human_RBP_ID_24637085 Human_Splice_Rec_188528,Human_Splice_Rec_188529,Human_Splice_Rec_188534,Human_Splice_Rec_188535,Human_Splice_Rec_188542,Human_Splice_Rec_188543,Human_Splice_Rec_188548,Human_Splice_Rec_188549,Human_Splice_Rec_188556,Human_Splice_Rec_188557,Human_Splice_Rec_188564,Human_Splice_Rec_188565,Human_Splice_Rec_188574,Human_Splice_Rec_188575,Human_Splice_Rec_188582,Human_Splice_Rec_188583,Human_Splice_Rec_188588,Human_Splice_Rec_188589,Human_Splice_Rec_188594,Human_Splice_Rec_188595 RMVar_hsa_circ_40753,RMVar_hsa_circ_266318,RMVar_hsa_circ_355885,RMVar_hsa_circ_65724,RMVar_hsa_circ_139625,RMVar_hsa_circ_139626,RMVar_hsa_circ_139627 102912 RMVar_ID_102912 Human_SNP_ID_50554363 m1A Human chr1 - 219968869 219968869 219968869 CCCTTCAAACCACTCTGTGAACTGCAGCCTGGAGCCAAATGTGTCTGTGGCAAGAACCCTGCCAA CCCTTCAAACCACTCTGTGAACTGCAGCCTGGGGCCAAATGTGTCTGTGGCAAGAACCCTGCCAA T C EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:219968819..219968920 26863196 MeRIP-seq:(Medium) rs746770023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741245,Human_RBP_ID_5162197,Human_RBP_ID_8298531,Human_RBP_ID_8743227,Human_RBP_ID_9270595,Human_RBP_ID_10777552,Human_RBP_ID_17181501,Human_RBP_ID_17221993,Human_RBP_ID_18187369,Human_RBP_ID_18562941,Human_RBP_ID_22427786,Human_RBP_ID_22782151,Human_RBP_ID_23206282,Human_RBP_ID_26801527,Human_RBP_ID_26853017 Human_Splice_Rec_188752,Human_Splice_Rec_188754 Human_miRNA_ID_2953171,Human_miRNA_ID_2956914 RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643 102913 RMVar_ID_102913 Human_SNP_ID_50561350 m1A Human chr1 - 219997245 219997244 219997246 TTCCTTGGTCCTTTACAATAGAGTGGCTGTTCAAGGAGATGTGGTTCGTGAATTAAAAGCCAAGA TTCCTTGGTCCTTTACAATAGAGTGGCTGTT__AGGAGATGTGGTTCGTGAATTAAAAGCCAAGA TTG T EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:219997194..219997368 26863196 MeRIP-seq:(Medium) rs764733186 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10778043,Human_RBP_ID_17739174 Human_Splice_Rec_188724,Human_Splice_Rec_188794,Human_Splice_Rec_188806 RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170,RMVar_hsa_circ_267770,RMVar_hsa_circ_375651,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_139650,RMVar_hsa_circ_139651 102914 RMVar_ID_102914 Human_SNP_ID_50561351 m1A Human chr1 - 219997245 219997245 219997245 TTCCTTGGTCCTTTACAATAGAGTGGCTGTTCAAGGAGATGTGGTTCGTGAATTAAAAGCCAAGA TTCCTTGGTCCTTTACAATAGAGTGGCTGTTCCAGGAGATGTGGTTCGTGAATTAAAAGCCAAGA T G EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:219997194..219997368 26863196 MeRIP-seq:(Medium) rs755807940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10778043,Human_RBP_ID_17739174 Human_Splice_Rec_188724,Human_Splice_Rec_188794,Human_Splice_Rec_188806 RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170,RMVar_hsa_circ_267770,RMVar_hsa_circ_375651,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_139650,RMVar_hsa_circ_139651 102915 RMVar_ID_102915 Human_SNP_ID_50562255 m1A Human chr1 - 220001092 220001092 220001092 CGGATATGTGTATAAAAATAAATGGTCTTTCTATCCCAGGGTTTAGAATATATTTCTTTACAGAT CGGATATGTGTATAAAAATAAATGGTCTTTCTGTCCCAGGGTTTAGAATATATTTCTTTACAGAT T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220001090..220001197 26863196 MeRIP-seq:(Medium) rs757822654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170,RMVar_hsa_circ_375651,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_139650,RMVar_hsa_circ_139651 102916 RMVar_ID_102916 Human_SNP_ID_50562256 m1A Human chr1 - 220001092 220001092 220001092 CGGATATGTGTATAAAAATAAATGGTCTTTCTATCCCAGGGTTTAGAATATATTTCTTTACAGAT CGGATATGTGTATAAAAATAAATGGTCTTTCTCTCCCAGGGTTTAGAATATATTTCTTTACAGAT T G EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220001090..220001197 26863196 MeRIP-seq:(Medium) rs757822654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170,RMVar_hsa_circ_375651,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_139650,RMVar_hsa_circ_139651 102917 RMVar_ID_102917 Human_SNP_ID_50563676 m1A Human chr1 - 220006313 220006312 220006314 ATTTCTTTGAATACTTTTAATCTTATATCTAGAAATGCAGATGGAAAAATCATATCTCTTGATGC ATTTCTTTGAATACTTTTAATCTTATATCTA__AATGCAGATGGAAAAATCATATCTCTTGATGC TTC T EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:220006301..220006325 32194978 MeRIP-seq:(Medium) rs1448106481 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17222008 Human_Splice_Rec_188718,Human_Splice_Rec_188788,Human_Splice_Rec_188800 RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_34170,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_70272,RMVar_hsa_circ_139652,RMVar_hsa_circ_119705,RMVar_hsa_circ_139650,RMVar_hsa_circ_318108,RMVar_hsa_circ_301463,RMVar_hsa_circ_139653,RMVar_hsa_circ_139654,RMVar_hsa_circ_139656,RMVar_hsa_circ_273657,RMVar_hsa_circ_361340,RMVar_hsa_circ_73027,RMVar_hsa_circ_139655,RMVar_hsa_circ_288040,RMVar_hsa_circ_139657 102918 RMVar_ID_102918 Human_SNP_ID_50563887 m1A Human chr1 - 220007205 220007205 220007205 AAATTGGGGCAACCTCAACATTACAAAAATACACAAGTAAGAACTTTTTGTTTGTTTTCAAATAA AAATTGGGGCAACCTCAACATTACAAAAATACGCAAGTAAGAACTTTTTGTTTGTTTTCAAATAA T C EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:220007201..220007250 32194978 MeRIP-seq:(Medium) rs1446426869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17222009 Human_Splice_Rec_188717,Human_Splice_Rec_188787,Human_Splice_Rec_188799 RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_34170,RMVar_hsa_circ_295947,RMVar_hsa_circ_139652,RMVar_hsa_circ_119705,RMVar_hsa_circ_139650,RMVar_hsa_circ_318108,RMVar_hsa_circ_301463,RMVar_hsa_circ_139653,RMVar_hsa_circ_139654,RMVar_hsa_circ_139656,RMVar_hsa_circ_273657,RMVar_hsa_circ_361340,RMVar_hsa_circ_73027,RMVar_hsa_circ_139655,RMVar_hsa_circ_288040,RMVar_hsa_circ_139657 102919 RMVar_ID_102919 Human_SNP_ID_50573737 m1A Human chr1 - 220046406 220046406 220046406 TTCTGGCACGAGCCAGGCGTACTGACAGGTGGACCAGCGGACTGGTGGAGATGGCGACGCTCTCT TTCTGGCACGAGCCAGGCGTACTGACAGGTGGGCCAGCGGACTGGTGGAGATGGCGACGCTCTCT T C EPRS1 Ensembl:ENSG00000136628 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220046326..220046525 26863196 MeRIP-seq:(Medium) rs1300169807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223987,Human_RBP_ID_341864,Human_RBP_ID_746587,Human_RBP_ID_4074754,Human_RBP_ID_5312832,Human_RBP_ID_5485436,Human_RBP_ID_8743296,Human_RBP_ID_9270637,Human_RBP_ID_10778998,Human_RBP_ID_17338663 Human_Splice_Rec_188691,Human_Splice_Rec_188759,Human_Splice_Rec_188807 102920 RMVar_ID_102920 Human_SNP_ID_50573744 m1A Human chr1 - 220046424 220046424 220046424 TCGCGGGGTCCTCCGTAGTTCTGGCACGAGCCAGGCGTACTGACAGGTGGACCAGCGGACTGGTG TCGCGGGGTCCTCCGTAGTTCTGGCACGAGCCCGGCGTACTGACAGGTGGACCAGCGGACTGGTG T G EPRS1 Ensembl:ENSG00000136628 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220046373..220046477 26863196 MeRIP-seq:(Medium) rs768550044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223987,Human_RBP_ID_746587,Human_RBP_ID_1421047,Human_RBP_ID_4074755,Human_RBP_ID_8754358,Human_RBP_ID_9270638 Human_Splice_Rec_188691,Human_Splice_Rec_188759,Human_Splice_Rec_188807 102921 RMVar_ID_102921 Human_SNP_ID_50573772 m1A Human chr1 + 220046461 220046461 220046461 CGTGCCAGAACTACGGAGGACCCCGCGAAAGGAAGAAGATGCAACGTGTGCGCGTACCCGACGCC CGTGCCAGAACTACGGAGGACCCCGCGAAAGGGAGAAGATGCAACGTGTGCGCGTACCCGACGCC A G lnc-IARS2-2 RNACentral:URS00008C0502 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:220046351..220046572 26863196 MeRIP-seq:(Medium) rs1486523588 Functional Loss SNV dbSNP153 33..33 33 - - - 102922 RMVar_ID_102922 Human_SNP_ID_50573774 m1A Human chr1 + 220046465 220046465 220046465 CCAGAACTACGGAGGACCCCGCGAAAGGAAGAAGATGCAACGTGTGCGCGTACCCGACGCCGCCG CCAGAACTACGGAGGACCCCGCGAAAGGAAGAGGATGCAACGTGTGCGCGTACCCGACGCCGCCG A G lnc-IARS2-2 RNACentral:URS00008C0502 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:220046326..220046603 26863196 MeRIP-seq:(Medium) rs1213853335 Functional Loss SNV dbSNP153 33..33 33 - - - 102923 RMVar_ID_102923 Human_SNP_ID_50576741 m1A Human chr1 - 220057933 220057933 220057933 GACATCGTGATCTGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACC GACATCGTGATCTGTCTGCCTCGGACTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGCACC T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878938199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341873 102924 RMVar_ID_102924 Human_SNP_ID_50576797 m1A Human chr1 - 220058113 220058113 220058113 AGAATGTAGTGGCGTGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG AGAATGTAGTGGCGTGATCTCGGCTCACTGCAGGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs967028299 Functional Loss SNV dbSNP153 33..33 33 - - - 102925 RMVar_ID_102925 Human_SNP_ID_50576968 m1A Human chr1 - 220058801 220058801 220058801 CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137752 Functional Loss SNV dbSNP153 33..33 33 - - - 102926 RMVar_ID_102926 Human_SNP_ID_50576969 m1A Human chr1 - 220058802 220058802 220058802 TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs3201546 Functional Loss SNV dbSNP153 33..33 33 - - - 102927 RMVar_ID_102927 Human_SNP_ID_50585998 m1A Human chr1 - 220094174 220094174 220094174 CCCCTGAGAGCGGGGTCCTCCGCTCCCGCCCCAGCTTGAAGGGGCAGGACCCCAGGAAACCAAGG CCCCTGAGAGCGGGGTCCTCCGCTCCCGCCCCTGCTTGAAGGGGCAGGACCCCAGGAAACCAAGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:220094126..220094350;chr1:220094126..220094310 26863196 MeRIP-seq:(Medium) rs1391545863 Functional Loss SNV dbSNP153 33..33 33 - - - 102928 RMVar_ID_102928 Human_SNP_ID_50586027 m1A Human chr1 - 220094200 220094200 220094200 GCAGCCCCCAACGCATGGTCCGGCAACCCCTGAGAGCGGGGTCCTCCGCTCCCGCCCCAGCTTGA GCAGCCCCCAACGCATGGTCCGGCAACCCCTGGGAGCGGGGTCCTCCGCTCCCGCCCCAGCTTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:220094151..220094297;chr1:220094151..220094302 26863196 MeRIP-seq:(Medium) rs760171886 Functional Loss SNV dbSNP153 33..33 33 - - - 102929 RMVar_ID_102929 Human_SNP_ID_50586084 m1A Human chr1 + 220094286 220094286 220094286 CCGCCCTGGCCACTGCCCGAAGTTTGTGGGGGACGCCCCGCCTTCCCTGCAGCCCGGGATGGCAA CCGCCCTGGCCACTGCCCGAAGTTTGTGGGGGTCGCCCCGCCTTCCCTGCAGCCCGGGATGGCAA A T IARS2 Ensembl:ENSG00000067704 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr1:220094151..220094399;chr1:220094194..220094300 26863410 MeRIP-seq:(Medium) rs1306230811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341900,Human_RBP_ID_746187,Human_RBP_ID_4025006,Human_RBP_ID_5234408,Human_RBP_ID_5312833,Human_RBP_ID_8754361,Human_RBP_ID_9270644,Human_RBP_ID_9320358,Human_RBP_ID_9359855,Human_RBP_ID_22428798 102930 RMVar_ID_102930 Human_SNP_ID_50586094 m1A Human chr1 - 220094301 220094301 220094301 CCTCTTCGTCGCCCCTTGCCATCCCGGGCTGCAGGGAAGGCGGGGCGTCCCCCACAAACTTCGGG CCTCTTCGTCGCCCCTTGCCATCCCGGGCTGCGGGGAAGGCGGGGCGTCCCCCACAAACTTCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:220094200..220094300 32194978 MeRIP-seq:(Medium) rs1167991391 Functional Loss SNV dbSNP153 33..33 33 - - - 102931 RMVar_ID_102931 Human_SNP_ID_50597037 m1A Human chr1 - 220137982 220137982 220137982 GCACGGATGGGCCAATTGCAACTTCGGTGAAGACATTGGAATCAGCTACCCACCAGCGAAGGACA GCACGGATGGGCCAATTGCAACTTCGGTGAAGGCATTGGAATCAGCTACCCACCAGCGAAGGACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220137877..220138002 26863196 MeRIP-seq:(Medium) rs1488422152 Functional Loss SNV dbSNP153 33..33 33 - - - 102932 RMVar_ID_102932 Human_SNP_ID_50597043 m1A Human chr1 - 220137995 220137995 220137995 CTGGCAGCATTGAGCACGGATGGGCCAATTGCAACTTCGGTGAAGACATTGGAATCAGCTACCCA CTGGCAGCATTGAGCACGGATGGGCCAATTGCCACTTCGGTGAAGACATTGGAATCAGCTACCCA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:220137951..220139051 26863410 MeRIP-seq:(Medium) rs1427231228 Functional Loss SNV dbSNP153 33..33 33 - - - 102933 RMVar_ID_102933 Human_SNP_ID_50598336 m1A Human chr1 + 220143102 220143102 220143102 AAAATGCAGCTGAGTACAAGGTTATCACTGTGATAGAACCTGGACTGCTTTTTGAGATAATAGAG AAAATGCAGCTGAGTACAAGGTTATCACTGTGGTAGAACCTGGACTGCTTTTTGAGATAATAGAG A G IARS2 Ensembl:ENSG00000067704 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:220143051..220143125 32194978 MeRIP-seq:(Medium) rs752232281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341970,Human_RBP_ID_1736681,Human_RBP_ID_3297173,Human_RBP_ID_8743356,Human_RBP_ID_8963104,Human_RBP_ID_10779805,Human_RBP_ID_23364753 Human_Splice_Rec_189007 Human_miRNA_ID_1994379,Human_miRNA_ID_2226874,Human_miRNA_ID_2284333,Human_miRNA_ID_2287332,Human_miRNA_ID_2502851,Human_miRNA_ID_2656103 RMVar_hsa_circ_61738,RMVar_hsa_circ_117805,RMVar_hsa_circ_116603,RMVar_hsa_circ_139686,RMVar_hsa_circ_139688,RMVar_hsa_circ_324852 102934 RMVar_ID_102934 Human_SNP_ID_50624051 m1A Human chr1 + 220253557 220253557 220253557 AGTCGGGGGTGGTGGGAGAAGGAGGAGGCGGCAAATCACTTATAAATGGCGCGGAAGCAGGACCC AGTCGGGGGTGGTGGGAGAAGGAGGAGGCGGCGAATCACTTATAAATGGCGCGGAAGCAGGACCC A G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879135241 Functional Loss SNV dbSNP153 33..33 33 - - - 102935 RMVar_ID_102935 Human_SNP_ID_50626958 m1A Human chr1 - 220267082 220267082 220267082 AGAGCTTGAAATTGCAAATTTTGGGTGGTCAGAACATGCTCCATCTTCCAGGAGGACCACTCTCT AGAGCTTGAAATTGCAAATTTTGGGTGGTCAGGACATGCTCCATCTTCCAGGAGGACCACTCTCT T C AURKAP1,RAB3GAP2 Ensembl:ENSG00000213033,Ensembl:ENSG00000118873 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1431538175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5091391,Human_RBP_ID_17456679 102936 RMVar_ID_102936 Human_SNP_ID_50628143 m1A Human chr1 + 220272354 220272354 220272354 CAATGGAGCAGGCCATGGCTCCAGGGAACCCCACTACGGCACTCACCTTACCTCACCACGCCCTG CAATGGAGCAGGCCATGGCTCCAGGGAACCCCGCTACGGCACTCACCTTACCTCACCACGCCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220272318..220272417 26863196 MeRIP-seq:(Medium) rs1184821254 Functional Loss SNV dbSNP153 33..33 33 - - - 102937 RMVar_ID_102937 Human_SNP_ID_50726662 m1A Human chr1 + 220690442 220690442 220690442 TGGGAGCCAGGCTCCGAAGCAAGGCGGAGAGCAGCCTCCTGCGCCGCGGGCCCCGAGGGCGAGGG TGGGAGCCAGGCTCCGAAGCAAGGCGGAGAGCGGCCTCCTGCGCCGCGGGCCCCGAGGGCGAGGG A G C1orf115 Ensembl:ENSG00000162817 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:220690346..220696635;chr1:220690351..220690581 26863196 MeRIP-seq:(Medium) rs867080655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743926,Human_RBP_ID_804382,Human_RBP_ID_4076383,Human_RBP_ID_23365248 RMVar_hsa_circ_139747,RMVar_hsa_circ_86427 102938 RMVar_ID_102938 Human_SNP_ID_50728572 m1A Human chr1 - 220697782 220697782 220697782 CTGGCTCCTGGACAGCAAACTTCTCTCTTCCAATGTCCTCTTGCCTCATTTCCATTTCCTTCACA CTGGCTCCTGGACAGCAAACTTCTCTCTTCCAGTGTCCTCTTGCCTCATTTCCATTTCCTTCACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220697731..220697834 26863196 MeRIP-seq:(Medium) rs1045673951 Functional Loss SNV dbSNP153 33..33 33 - - - 102939 RMVar_ID_102939 Human_SNP_ID_50728733 m1A Human chr1 + 220698632 220698632 220698632 TGTGCAGGCTGCTGACGAGCCCCAGGCAGCCCACAAGTTTCTCGTGGGGAGATGGAGGCAGAGCC TGTGCAGGCTGCTGACGAGCCCCAGGCAGCCCGCAAGTTTCTCGTGGGGAGATGGAGGCAGAGCC A G C1orf115 Ensembl:ENSG00000162817 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:220698586..220698715 26863196 MeRIP-seq:(Medium) rs1416978059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17739420,Human_RBP_ID_23365274 RMVar_hsa_circ_139747,RMVar_hsa_circ_86427 102940 RMVar_ID_102940 Human_SNP_ID_50740667 m1A Human chr1 - 220748349 220748349 220748349 AGAGCAGTTCCGCGGAGAGCGGGAATGCCTTAATGCGGTGACCAAGCCTGCGCGGTAATGGAGGA AGAGCAGTTCCGCGGAGAGCGGGAATGCCTTATTGCGGTGACCAAGCCTGCGCGGTAATGGAGGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:220748298..220748404 26863196 MeRIP-seq:(Medium) rs1238284323 Functional Loss SNV dbSNP153 33..33 33 - - - 102941 RMVar_ID_102941 Human_SNP_ID_50740745 m1A Human chr1 - 220748572 220748572 220748572 CCCCGAGCCACCTGGGCCAGGGCCGGGCTGGGAGGCCGAGGCGGGCCAGCGCGGAGGAGCTGGAA CCCCGAGCCACCTGGGCCAGGGCCGGGCTGGGGGGCCGAGGCGGGCCAGCGCGGAGGAGCTGGAA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:220748492..220748577 26863410 MeRIP-seq:(Medium) rs1281103448 Functional Loss SNV dbSNP153 33..33 33 - - - 102942 RMVar_ID_102942 Human_SNP_ID_50742562 m1A Human chr1 + 220755473 220755473 220755473 AGTACCAGGGTGGGTCAGGAGGCAGAGGGAGCAGGGGGAACATGTGGGCAAGGGCTTTTATTGTG AGTACCAGGGTGGGTCAGGAGGCAGAGGGAGCTGGGGGAACATGTGGGCAAGGGCTTTTATTGTG A T MTARC2 Ensembl:ENSG00000117791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220755422..220755533 26863196 MeRIP-seq:(Medium) rs982594665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139748,RMVar_hsa_circ_139749,RMVar_hsa_circ_355932 102943 RMVar_ID_102943 Human_SNP_ID_50745647 m1A Human chr1 + 220768619 220768619 220768619 TCAGGTCATTTGGCAAACCTGTATAGGGCCCCAGTCACTGTGGATGGGCTGGGGGGTCATGGGTG TCAGGTCATTTGGCAAACCTGTATAGGGCCCCGGTCACTGTGGATGGGCTGGGGGGTCATGGGTG A G MTARC2 Ensembl:ENSG00000117791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220768613..220768717 26863196 MeRIP-seq:(Medium) rs75742660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139749,RMVar_hsa_circ_338300,RMVar_hsa_circ_139751 102944 RMVar_ID_102944 Human_SNP_ID_50750257 m1A Human chr1 + 220786945 220786945 220786945 CTTGCCGCCGCCACCTCGCGGAGAAGCCAGCCATGGGCGCCGCCGGCTCCTCCGCGCTGGCGCGC CTTGCCGCCGCCACCTCGCGGAGAAGCCAGCCTTGGGCGCCGCCGGCTCCTCCGCGCTGGCGCGC A T MTARC1 Ensembl:ENSG00000186205 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:220786901..220787125 26863196 MeRIP-seq:(Medium) rs905438821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4025574,Human_RBP_ID_8298891 102945 RMVar_ID_102945 Human_SNP_ID_50750355 m1A Human chr1 + 220787171 220787171 220787171 TGTGAAATCCTGCAAGGGGGTGCCGGTGAGCGAGGCGGAGTGCACGGCCATGGGGCTGCGCAGCG TGTGAAATCCTGCAAGGGGGTGCCGGTGAGCGTGGCGGAGTGCACGGCCATGGGGCTGCGCAGCG A T AL445423.3,MTARC1 Ensembl:ENSG00000286231,Ensembl:ENSG00000186205 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:220786901..220787284 26863196 MeRIP-seq:(Medium) rs751207575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_342231,Human_RBP_ID_4076386,Human_RBP_ID_17739458 Human_Splice_Rec_189333,Human_Splice_Rec_189383 102946 RMVar_ID_102946 Human_SNP_ID_50753995 m1A Human chr1 + 220801564 220801564 220801564 TCCAGGAGAAAGGGGGGCACTGAGGGAGGGGTACATACACAGGGCTATGAAGGTATGAGAGAATG TCCAGGAGAAAGGGGGGCACTGAGGGAGGGGTGCATACACAGGGCTATGAAGGTATGAGAGAATG A G AL445423.3,MTARC1 Ensembl:ENSG00000286231,Ensembl:ENSG00000186205 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220801560..220801778 26863196 MeRIP-seq:(Medium) rs1231316244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11197606 RMVar_hsa_circ_139752,RMVar_hsa_circ_328226,RMVar_hsa_circ_332570,RMVar_hsa_circ_58302,RMVar_hsa_circ_139754 102947 RMVar_ID_102947 Human_SNP_ID_50756682 m1A Human chr1 - 220812646 220812646 220812646 GCATCTTTCCTCCTGTCTCCTCCATGTCTGTCACCTGAACCACCATCCTAGCCGTCACTTGGGCT GCATCTTTCCTCCTGTCTCCTCCATGTCTGTCTCCTGAACCACCATCCTAGCCGTCACTTGGGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:220812368..220812689;chr1:220812058..220812700 26863196 MeRIP-seq:(Medium) rs965944420 Functional Loss SNV dbSNP153 33..33 33 - - - 102948 RMVar_ID_102948 Human_SNP_ID_50772326 m1A Human chr1 + 220879900 220879900 220879900 CCGGGCTGGCTCCCTTCTACGCCTCCAACTTCAGCCTCTGGTCGGCCGCTTACTGCTCCTCGGCC CCGGGCTGGCTCCCTTCTACGCCTCCAACTTCGGCCTCTGGTCGGCCGCTTACTGCTCCTCGGCC A G AL445423.3,HLX Ensembl:ENSG00000286231,Ensembl:ENSG00000136630 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220879853..220879930 26863196 MeRIP-seq:(Medium) rs773259608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5485455,Human_RBP_ID_8743402 102949 RMVar_ID_102949 Human_SNP_ID_50772524 m1A Human chr1 + 220880250 220880250 220880250 CACCATCACCCGCAACAACAACAGCAGCAGCAACAGCCGCAGCAGCAACAGCCTCCGCCTCCGCC CACCATCACCCGCAACAACAACAGCAGCAGCAGCAGCCGCAGCAGCAACAGCCTCCGCCTCCGCC A G AL445423.3,HLX Ensembl:ENSG00000286231,Ensembl:ENSG00000136630 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220880217..220880374 26863196 MeRIP-seq:(Medium) rs762960568 Functional Loss SNV dbSNP153 33..33 33 - - - 102950 RMVar_ID_102950 Human_SNP_ID_50773816 m1A Human chr1 + 220884313 220884313 220884313 CGAGAAGCCATCAGGTGGAGCCCCGGCTGCGGATGGCGAGCAGGACGAGAGGAGCCCCAGCCGTT CGAGAAGCCATCAGGTGGAGCCCCGGCTGCGGTTGGCGAGCAGGACGAGAGGAGCCCCAGCCGTT A T AL445423.3,HLX Ensembl:ENSG00000286231,Ensembl:ENSG00000136630 Protein coding,Protein coding 3'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220884264..220884403 26863196 MeRIP-seq:(Medium) rs1329738259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119926,RMVar_hsa_circ_139756 102951 RMVar_ID_102951 Human_SNP_ID_51150516 m1A Human chr1 + 222465062 222465062 222465062 ACTGGTCTTGTAAACCAGGGGTCGCGAGTTCGATCCTCGCTGGGGCCTCCTGTTGGCTTACTTTT ACTGGTCTTGTAAACCAGGGGTCGCGAGTTCGGTCCTCGCTGGGGCCTCCTGTTGGCTTACTTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1033266032 Functional Loss SNV dbSNP153 33..33 33 - - - 102952 RMVar_ID_102952 Human_SNP_ID_51180944 m1A Human chr1 - 222589732 222589732 222589732 TGAGTTTAGCTTTACTGAGGAGCTCTAAATTTAGGCGGGTAAGTGCCGCAGATATCGCCCGTGGT TGAGTTTAGCTTTACTGAGGAGCTCTAAATTTGGGCGGGTAAGTGCCGCAGATATCGCCCGTGGT T C TAF1A Ensembl:ENSG00000143498 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:222588472..222589733 26863196 MeRIP-seq:(Medium) rs576207992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5537375 Human_Splice_Rec_189615,Human_Splice_Rec_189635,Human_Splice_Rec_189657,Human_Splice_Rec_189677,Human_Splice_Rec_189691,Human_Splice_Rec_189709 102953 RMVar_ID_102953 Human_SNP_ID_51199914 m1A Human chr1 - 222669717 222669715 222669717 TGTACCACAGAATTCAGAGTCCAGCACATCACACTGACGTATAGGACTCCTTGGGATACAGGTTT TGTACCACAGAATTCAGAGTCCAGCACATCAC__TGACGTATAGGACTCCTTGGGATACAGGTTT AGT A AIDA Ensembl:ENSG00000186063 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:222669694..222669773 26863196 MeRIP-seq:(Medium) rs4011740 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_98891,Human_RBP_ID_342449,Human_RBP_ID_1737178,Human_RBP_ID_10786817,Human_RBP_ID_17215773,Human_RBP_ID_17333300,Human_RBP_ID_17739640,Human_RBP_ID_27402616 Human_miRNA_ID_641151,Human_miRNA_ID_2439316 102954 RMVar_ID_102954 Human_SNP_ID_51210125 m1A Human chr1 + 222712443 222712443 222712443 GGCCAGGAGGAACCGCTACGGCCACCACCGCCACCCGCCGAGGAGCCGCCCAAGCCCATTTGCCG GGCCAGGAGGAACCGCTACGGCCACCACCGCCCCCCGCCGAGGAGCCGCCCAAGCCCATTTGCCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:222712392..222712500;chr1:222712388..222712474 26863196 MeRIP-seq:(Medium) rs959342490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18563523 102955 RMVar_ID_102955 Human_SNP_ID_51235444 m1A Human chr1 + 222815119 222815119 222815119 GCAGCCGGAACGTTGCAGGCACTTGTTTCCTCAGTGGATGCCTTTCGGCGCGCCGCCGCCCGGCG GCAGCCGGAACGTTGCAGGCACTTGTTTCCTCCGTGGATGCCTTTCGGCGCGCCGCCGCCCGGCG A C AL392172.1,AC093152.1 Ensembl:ENSG00000228106,Ensembl:ENSG00000278610 lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:222815068..222823900 26863196 MeRIP-seq:(Medium) rs994623848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8299134,Human_RBP_ID_19040230 Human_Splice_Rec_190221,Human_Splice_Rec_190223,Human_Splice_Rec_190231,Human_Splice_Rec_190237,Human_Splice_Rec_190241,Human_Splice_Rec_190243,Human_Splice_Rec_190247 RMVar_hsa_circ_139789,RMVar_hsa_circ_95000 102956 RMVar_ID_102956 Human_SNP_ID_51284845 m1A Human chr1 + 223029067 223029029 223029068 TCGGGGCATGGAAATAAGGGATTGGGACGCAGAGATAAGAGGTTGGGGCGTGGAAATAAGCGATT __________________________________ATAAGAGGTTGGGGCGTGGAAATAAGCGATT AATAGGTCGGGGCATGGAAATAAGGGATTGGGACGCAGAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:223029022..223029087 26863196 MeRIP-seq:(Medium) rs1457523412 Functional Loss DEL dbSNP153 1..34 33 - - - 102957 RMVar_ID_102957 Human_SNP_ID_51443574 m1A Human chr1 + 223712678 223712678 223712678 GGGCATCGCGGCCAAGCTGGCGAAGGACCGGGAGGCGGCCGAGGGGCTGGGCTCCCACGACAGGG GGGCATCGCGGCCAAGCTGGCGAAGGACCGGGCGGCGGCCGAGGGGCTGGGCTCCCACGACAGGG A C CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:223712445..223712905;chr1:223712474..223712804;chr1:223712531..223712750 26863196 MeRIP-seq:(Medium) rs1297410443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22688,Human_RBP_ID_743941,Human_RBP_ID_802859,Human_RBP_ID_3937343,Human_RBP_ID_4074766,Human_RBP_ID_8755373,Human_RBP_ID_9270654,Human_RBP_ID_9320360,Human_RBP_ID_22024257,Human_RBP_ID_26312744 RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 102958 RMVar_ID_102958 Human_SNP_ID_51443618 m1A Human chr1 - 223712723 223712723 223712723 ACTCGTTCCGCAGCGCCTCGTAGTCCTGGTTGAGGTACTTGATGGCCCTGTCGTGGGAGCCCAGC ACTCGTTCCGCAGCGCCTCGTAGTCCTGGTTGGGGTACTTGATGGCCCTGTCGTGGGAGCCCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:223712442..223712903 26863196 MeRIP-seq:(Medium) rs749441899 Functional Loss SNV dbSNP153 33..33 33 - - - 102959 RMVar_ID_102959 Human_SNP_ID_51444828 m1A Human chr1 + 223717821 223717821 223717821 ATTGGAGGAGCCACCCGCACAGACATCTGCCAAGGAGCCCTGGGTAAGTGATAGATTCAGAGCAA ATTGGAGGAGCCACCCGCACAGACATCTGCCACGGAGCCCTGGGTAAGTGATAGATTCAGAGCAA A C CAPN2 Ensembl:ENSG00000162909 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:223717801..223717825 26863196 MeRIP-seq:(Medium) rs759831586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743942,Human_RBP_ID_802861,Human_RBP_ID_853213,Human_RBP_ID_3937344 Human_Splice_Rec_190580,Human_Splice_Rec_190581,Human_Splice_Rec_190620,Human_Splice_Rec_190621,Human_Splice_Rec_190628,Human_Splice_Rec_190629 Human_miRNA_ID_593519,Human_miRNA_ID_2216773 RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 102960 RMVar_ID_102960 Human_SNP_ID_51468324 m1A Human chr1 + 223813325 223813324 223813326 AGCCTCATTTCAGGGCCCCACCTGGGACCACAACACTAGAAGCCCTCTACCTCCGAAATTTTCAA AGCCTCATTTCAGGGCCCCACCTGGGACCACA__ACTAGAAGCCCTCTACCTCCGAAATTTTCAA AAC A lnc-CAPN2-2 RNACentral:URS00008BEE3B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:223813318..223813480 26863196 MeRIP-seq:(Medium) rs1558100646 Functional Loss DEL dbSNP153 33..34 33 - - - 102961 RMVar_ID_102961 Human_SNP_ID_51476324 m1A Human chr1 + 223845760 223845760 223845760 GAGGGTCGCGGATGCGGGGGAGGGGAGCGGAGAGCGAGGCCGCCCGGACCTGTTGCGAGGCGGCG GAGGGTCGCGGATGCGGGGGAGGGGAGCGGAGTGCGAGGCCGCCCGGACCTGTTGCGAGGCGGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HeLa cell line,mRNA;HEK293T,untreat control chr1:223845712..223845940;chr1:223845721..223845822 26863196,26863410 MeRIP-seq:(Medium) rs1339393367 Functional Loss SNV dbSNP153 33..33 33 - - - 102962 RMVar_ID_102962 Human_SNP_ID_51476510 m1A Human chr1 - 223846149 223846149 223846149 GCGCGCTCCAGCCGCTCCGCCGCGCGGCCCCGACCGCACTTCAGTCCGGGGCGAAGAAAGAAAAG GCGCGCTCCAGCCGCTCCGCCGCGCGGCCCCGCCCGCACTTCAGTCCGGGGCGAAGAAAGAAAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:223846101..223846601 26863196 MeRIP-seq:(Medium) rs1158497424 Functional Loss SNV dbSNP153 33..33 33 - - - 102963 RMVar_ID_102963 Human_SNP_ID_51476532 m1A Human chr1 + 223846210 223846210 223846210 GCGCGCCTCCTAGCGGAGCCGGGGCAATTGGAAGGCCGCGCCTCAGGAAAACAGGATGGTAGTGA GCGCGCCTCCTAGCGGAGCCGGGGCAATTGGAGGGCCGCGCCTCAGGAAAACAGGATGGTAGTGA A G lnc-CAPN2-3,lnc-CAPN2-3:2 RNACentral:URS0000D58041,RNACentral:URS00008B820D lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:223846167..223846359 26863196 MeRIP-seq:(Medium) rs1378977977 Functional Loss SNV dbSNP153 33..33 33 - - - 102964 RMVar_ID_102964 Human_SNP_ID_51501016 m1A Human chr1 + 223951991 223951991 223951991 GACGGGAGGCACAGGCTGGGCCTGGAGGGGCCACCAAGATGCAGGAGTTGGGCCTGGAGAGGCTG GACGGGAGGCACAGGCTGGGCCTGGAGGGGCCCCCAAGATGCAGGAGTTGGGCCTGGAGAGGCTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:223951942..223952015 26863196 MeRIP-seq:(Medium) rs1266903237 Functional Loss SNV dbSNP153 33..33 33 - - - 102965 RMVar_ID_102965 Human_SNP_ID_51511210 m1A Human chr1 + 223992537 223992537 223992537 TCGCTCTTACCAGTCCCCACTCTGACGAGAAAACTGCCCAGCTCCAGGCACCATAGCGCCCCAGT TCGCTCTTACCAGTCCCCACTCTGACGAGAAATCTGCCCAGCTCCAGGCACCATAGCGCCCCAGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:223992467..223992555 26863196 MeRIP-seq:(Medium) rs1446081480 Functional Loss SNV dbSNP153 33..33 33 - - - 102966 RMVar_ID_102966 Human_SNP_ID_51512693 m1A Human chr1 - 223998954 223998954 223998954 TCAAAAAGAATTTCTCTGCTAATATTACTCTTATGTGCTCCTTAGTCTCATGCCTCTCCCATTTC TCAAAAAGAATTTCTCTGCTAATATTACTCTTGTGTGCTCCTTAGTCTCATGCCTCTCCCATTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:223998904..223999079 26863196 MeRIP-seq:(Medium) rs190206746 Functional Loss SNV dbSNP153 33..33 33 - - - 102967 RMVar_ID_102967 Human_SNP_ID_51512707 m1A Human chr1 + 223999026 223999026 223999026 GGTCATGAATTTTATGGTATAGGAATAGAAAGAGGGGTTAATCCAGAATGGGATTTGAGTTGGAA GGTCATGAATTTTATGGTATAGGAATAGAAAGGGGGGTTAATCCAGAATGGGATTTGAGTTGGAA A G AC138393.1 Ensembl:ENSG00000185495 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:223998942..223999215 26863196 MeRIP-seq:(Medium) rs1005518198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5762200,Human_RBP_ID_9553085,Human_RBP_ID_10790606 102968 RMVar_ID_102968 Human_SNP_ID_51515272 m1A Human chr1 - 224011386 224011386 224011386 AGGTTCCTGCTCGATTTCTAGTTTGTTCGTTCATTCATTCTTTTGTTCTTTCTCTCTCCTTCTCT AGGTTCCTGCTCGATTTCTAGTTTGTTCGTTCGTTCATTCTTTTGTTCTTTCTCTCTCCTTCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224011336..224011450 26863196 MeRIP-seq:(Medium) rs1445892588 Functional Loss SNV dbSNP153 33..33 33 - - - 102969 RMVar_ID_102969 Human_SNP_ID_51515386 m1A Human chr1 - 224011773 224011754 224011774 TCATTCCATTCGAGTGCGTTCCATTCCATTCCATTCTGTTCCATTCCATTCGGGTCCATTCCATT TCATTCCATTCGAGTGCGTTCCATTCCATTC____________________GGGTCCATTCCATT CGAATGGAATGGAACAGAATG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224011722..224011966 26863196 MeRIP-seq:(Medium) rs1250738192 Functional Loss DEL dbSNP153 32..51 33 - - - 102970 RMVar_ID_102970 Human_SNP_ID_51515611 m1A Human chr1 + 224011916 224011916 224011916 GGAATGGACACGAATGGAACAGAATGGAACGGAATAGACTCGAATGGGATGGAATGGAATTGAAT GGAATGGACACGAATGGAACAGAATGGAACGGGATAGACTCGAATGGGATGGAATGGAATTGAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224011708..224012232 26863196 MeRIP-seq:(Medium) rs1383731455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23366444 102971 RMVar_ID_102971 Human_SNP_ID_51515613 m1A Human chr1 + 224011919 224011919 224011919 ATGGACACGAATGGAACAGAATGGAACGGAATAGACTCGAATGGGATGGAATGGAATTGAATGGA ATGGACACGAATGGAACAGAATGGAACGGAATGGACTCGAATGGGATGGAATGGAATTGAATGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224011731..224011973 26863196 MeRIP-seq:(Medium) rs547456594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23366444 102972 RMVar_ID_102972 Human_SNP_ID_51516845 m1A Human chr1 - 224013496 224013496 224013496 TTCAACTGTATTCCATTCGAGTCCATTCCATTACATTTTATTCCATTCCATTCCATTCCATTCCA TTCAACTGTATTCCATTCGAGTCCATTCCATTTCATTTTATTCCATTCCATTCCATTCCATTCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224012318..224013728 26863196 MeRIP-seq:(Medium) rs150126593 Functional Loss SNV dbSNP153 33..33 33 - - - 102973 RMVar_ID_102973 Human_SNP_ID_51516846 m1A Human chr1 - 224013496 224013496 224013496 TTCAACTGTATTCCATTCGAGTCCATTCCATTACATTTTATTCCATTCCATTCCATTCCATTCCA TTCAACTGTATTCCATTCGAGTCCATTCCATTCCATTTTATTCCATTCCATTCCATTCCATTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224012318..224013728 26863196 MeRIP-seq:(Medium) rs150126593 Functional Loss SNV dbSNP153 33..33 33 - - - 102974 RMVar_ID_102974 Human_SNP_ID_51517401 m1A Human chr1 - 224013938 224013938 224013938 CCGTTCCATCCGAGTCCATTCCGTTCCATTCCATTTCATTCGCGTCCATTCCGTTCCATTCCATT CCGTTCCATCCGAGTCCATTCCGTTCCATTCCGTTTCATTCGCGTCCATTCCGTTCCATTCCATT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224013782..224014095 26863196 MeRIP-seq:(Medium) rs1438317824 Functional Loss SNV dbSNP153 33..33 33 - - - 102975 RMVar_ID_102975 Human_SNP_ID_51517416 m1A Human chr1 + 224013962 224013959 224013963 GAATGAAATGGAATGGAACGGAATGGACTCGGATGGAACGGAACGGAATGGAACGGAATGGAATG GAATGAAATGGAATGGAACGGAATGGACTC____GGAACGGAACGGAATGGAACGGAATGGAATG CGGAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224012301..224014671 26863196 MeRIP-seq:(Medium) rs538918336 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_23366496 102976 RMVar_ID_102976 Human_SNP_ID_51517423 m1A Human chr1 + 224013962 224013962 224013962 GAATGAAATGGAATGGAACGGAATGGACTCGGATGGAACGGAACGGAATGGAACGGAATGGAATG GAATGAAATGGAATGGAACGGAATGGACTCGGGTGGAACGGAACGGAATGGAACGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224012301..224014671 26863196 MeRIP-seq:(Medium) rs1376915161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23366496 102977 RMVar_ID_102977 Human_SNP_ID_51518202 m1A Human chr1 + 224014846 224014844 224014847 GACTCGAATGGAATGGAATGGAATGGAACCGAAAGGAATGGAATGGAATGGAATGGAATGGAATC GACTCGAATGGAATGGAATGGAATGGAACCG___GGAATGGAATGGAATGGAATGGAATGGAATC GAAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224014727..224015010 26863196 MeRIP-seq:(Medium) rs1369992463 Functional Loss DEL dbSNP153 32..34 33 - - - 102978 RMVar_ID_102978 Human_SNP_ID_51518204 m1A Human chr1 + 224014846 224014846 224014846 GACTCGAATGGAATGGAATGGAATGGAACCGAAAGGAATGGAATGGAATGGAATGGAATGGAATC GACTCGAATGGAATGGAATGGAATGGAACCGAGAGGAATGGAATGGAATGGAATGGAATGGAATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224014727..224015010 26863196 MeRIP-seq:(Medium) rs1402123127 Functional Loss SNV dbSNP153 33..33 33 - - - 102979 RMVar_ID_102979 Human_SNP_ID_51518747 m1A Human chr1 - 224015456 224015456 224015456 AGTCCATTCCATTGCATTCCATTCCATTCGAGACCATTCCATTGTATTCCATCCCAATCCTTTCG AGTCCATTCCATTGCATTCCATTCCATTCGAGTCCATTCCATTGTATTCCATCCCAATCCTTTCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224015411..224015607 26863196 MeRIP-seq:(Medium) rs62652751 Functional Loss SNV dbSNP153 33..33 33 - - - 102980 RMVar_ID_102980 Human_SNP_ID_51518748 m1A Human chr1 - 224015456 224015456 224015456 AGTCCATTCCATTGCATTCCATTCCATTCGAGACCATTCCATTGTATTCCATCCCAATCCTTTCG AGTCCATTCCATTGCATTCCATTCCATTCGAGGCCATTCCATTGTATTCCATCCCAATCCTTTCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224015411..224015607 26863196 MeRIP-seq:(Medium) rs62652751 Functional Loss SNV dbSNP153 33..33 33 - - - 102981 RMVar_ID_102981 Human_SNP_ID_51518749 m1A Human chr1 - 224015456 224015456 224015456 AGTCCATTCCATTGCATTCCATTCCATTCGAGACCATTCCATTGTATTCCATCCCAATCCTTTCG AGTCCATTCCATTGCATTCCATTCCATTCGAGCCCATTCCATTGTATTCCATCCCAATCCTTTCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224015411..224015607 26863196 MeRIP-seq:(Medium) rs62652751 Functional Loss SNV dbSNP153 33..33 33 - - - 102982 RMVar_ID_102982 Human_SNP_ID_51519473 m1A Human chr1 - 224016355 224016351 224016356 CCATTCTATTCCATTTGAGTCCATTCCATTCCATTCTAGATCATTCCATCCCAACCCATTCCAAT CCATTCTATTCCATTTGAGTCCATTCCATTC_____TAGATCATTCCATCCCAACCCATTCCAAT AGAATG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224016307..224016380 26863196 MeRIP-seq:(Medium) rs1255505295 Functional Loss DEL dbSNP153 32..36 33 - - - 102983 RMVar_ID_102983 Human_SNP_ID_51519595 m1A Human chr1 - 224016505 224016496 224016506 CCATTCCATTCGAGTCCATTCCATTCCATTCCATTCCATTCGAGTCCATTCCATTCTATTCCATT CCATTCCATTCGAGTCCATTCCATTCCATTC__________GAGTCCATTCCATTCTATTCCATT CGAATGGAATG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224016454..224016527 26863196 MeRIP-seq:(Medium) rs746611362 Functional Loss DEL dbSNP153 32..41 33 - - - 102984 RMVar_ID_102984 Human_SNP_ID_51519596 m1A Human chr1 - 224016505 224016496 224016506 CCATTCCATTCGAGTCCATTCCATTCCATTCCATTCCATTCGAGTCCATTCCATTCTATTCCATT CCATTCCATTCGAGTCCATTCCATTCCATTC_____CATTCGAGTCCATTCCATTCTATTCCATT CGAATGGAATG CGAATG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224016454..224016527 26863196 MeRIP-seq:(Medium) rs746611362 Functional Loss DEL dbSNP153 32..36 33 - - - 102985 RMVar_ID_102985 Human_SNP_ID_51519605 m1A Human chr1 - 224016510 224016510 224016510 CCTTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATTCCATTCGAGTCCATTCCATTCTATT CCTTTCCATTCCATTCGAGTCCATTCCATTCCTTTCCATTCCATTCGAGTCCATTCCATTCTATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224016286..224016554 26863196 MeRIP-seq:(Medium) rs1301940324 Functional Loss SNV dbSNP153 33..33 33 - - - 102986 RMVar_ID_102986 Human_SNP_ID_51519606 m1A Human chr1 - 224016510 224016510 224016510 CCTTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATTCCATTCGAGTCCATTCCATTCTATT CCTTTCCATTCCATTCGAGTCCATTCCATTCCGTTCCATTCCATTCGAGTCCATTCCATTCTATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224016286..224016554 26863196 MeRIP-seq:(Medium) rs1301940324 Functional Loss SNV dbSNP153 33..33 33 - - - 102987 RMVar_ID_102987 Human_SNP_ID_51555053 m1A Human chr1 + 224161213 224161213 224161213 CCATAATATTTTCTAGGATCCGGGAACTCCCTATATTGTCTATTTCCAACATTATATAATTTTAA CCATAATATTTTCTAGGATCCGGGAACTCCCTGTATTGTCTATTTCCAACATTATATAATTTTAA A G FBXO28 Ensembl:ENSG00000143756 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6426162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743336,Human_RBP_ID_26390432 Human_miRNA_ID_149529,Human_miRNA_ID_1201499,Human_miRNA_ID_1209133,Human_miRNA_ID_2349108,Human_miRNA_ID_2580270 RMVar_hsa_circ_90093,RMVar_hsa_circ_139838,RMVar_hsa_circ_122343,RMVar_hsa_circ_139839 102988 RMVar_ID_102988 Human_SNP_ID_51555054 m1A Human chr1 + 224161213 224161213 224161213 CCATAATATTTTCTAGGATCCGGGAACTCCCTATATTGTCTATTTCCAACATTATATAATTTTAA CCATAATATTTTCTAGGATCCGGGAACTCCCTTTATTGTCTATTTCCAACATTATATAATTTTAA A T FBXO28 Ensembl:ENSG00000143756 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6426162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743336,Human_RBP_ID_26390432 Human_miRNA_ID_149529,Human_miRNA_ID_1201499,Human_miRNA_ID_1209133,Human_miRNA_ID_2349108,Human_miRNA_ID_2580270 RMVar_hsa_circ_90093,RMVar_hsa_circ_139838,RMVar_hsa_circ_122343,RMVar_hsa_circ_139839 102989 RMVar_ID_102989 Human_SNP_ID_51560722 m1A Human chr1 + 224183300 224183300 224183300 CGCCGCCACCTCTGAGCAGCCGGCTGGGAGCGAGAGCCGACAGCTAGTCTGCAAGCCACCGCTGT CGCCGCCACCTCTGAGCAGCCGGCTGGGAGCGTGAGCCGACAGCTAGTCTGCAAGCCACCGCTGT A T DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:224183226..224183679;chr1:224183226..224183463;chr1:224183201..224183679 26863196 MeRIP-seq:(Medium) rs1467745738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224171,Human_RBP_ID_1421681,Human_RBP_ID_4026934 102990 RMVar_ID_102990 Human_SNP_ID_51560742 m1A Human chr1 - 224183350 224183350 224183350 CGGTGTAGACCCACTCGAAGTCTTCCCGCGAGACGCGGCTCCCCATGGCGACAGCGGTGGCTTGC CGGTGTAGACCCACTCGAAGTCTTCCCGCGAGTCGCGGCTCCCCATGGCGACAGCGGTGGCTTGC T A - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:224183251..224183375 26863196 MeRIP-seq:(Medium) rs938805576 Functional Loss SNV dbSNP153 33..33 33 - - - 102991 RMVar_ID_102991 Human_SNP_ID_51560748 m1A Human chr1 - 224183370 224183370 224183370 CCGGTCGGCGTGCGGCTGGTCGGTGTAGACCCACTCGAAGTCTTCCCGCGAGACGCGGCTCCCCA CCGGTCGGCGTGCGGCTGGTCGGTGTAGACCCGCTCGAAGTCTTCCCGCGAGACGCGGCTCCCCA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:224183274..224183373 26863410 MeRIP-seq:(Medium) rs1357215169 Functional Loss SNV dbSNP153 33..33 33 - - - 102992 RMVar_ID_102992 Human_SNP_ID_51578771 m1A Human chr1 - 224252064 224252064 224252064 GTAAACAGGGCGTGGGAGTTGGAAGAATGTGTAGGAAGAATAAAACCAGAAAGGAAGATGGTCAG GTAAACAGGGCGTGGGAGTTGGAAGAATGTGTGGGAAGAATAAAACCAGAAAGGAAGATGGTCAG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224252014..224252179 26863196 MeRIP-seq:(Medium) rs575853726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22855206 RMVar_hsa_circ_318367,RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_367791,RMVar_hsa_circ_275747,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,RMVar_hsa_circ_139848,RMVar_hsa_circ_272947,RMVar_hsa_circ_320876,RMVar_hsa_circ_355092,RMVar_hsa_circ_367033,RMVar_hsa_circ_298650,RMVar_hsa_circ_73989,RMVar_hsa_circ_139853,RMVar_hsa_circ_18778,RMVar_hsa_circ_54524,RMVar_hsa_circ_139854,RMVar_hsa_circ_139855,RMVar_hsa_circ_139852 102993 RMVar_ID_102993 Human_SNP_ID_51597335 m1A Human chr1 - 224330088 224330088 224330088 CCAGACCTGCAGGGTTCGTGGATAATAAACTCAAGCAGCGAGTCATCCAGGTGTGTATTCTGCAC CCAGACCTGCAGGGTTCGTGGATAATAAACTCTAGCAGCGAGTCATCCAGGTGTGTATTCTGCAC T A NVL Ensembl:ENSG00000143748 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224317740..224330108 26863196 MeRIP-seq:(Medium) rs185167238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3298497,Human_RBP_ID_4077168,Human_RBP_ID_5537395,Human_RBP_ID_17740108,Human_RBP_ID_19035942 Human_Splice_Rec_191033,Human_Splice_Rec_191073,Human_Splice_Rec_191115,Human_Splice_Rec_191161,Human_Splice_Rec_191205,Human_Splice_Rec_191247,Human_Splice_Rec_191299,Human_Splice_Rec_191321,Human_Splice_Rec_191333,Human_Splice_Rec_191339,Human_Splice_Rec_191351,Human_Splice_Rec_191363,Human_Splice_Rec_191369,Human_Splice_Rec_191381,Human_Splice_Rec_191393,Human_Splice_Rec_191401,Human_Splice_Rec_191407 RMVar_hsa_circ_88659,RMVar_hsa_circ_139868 102994 RMVar_ID_102994 Human_SNP_ID_51597360 m1A Human chr1 - 224330118 224330118 224330118 CTGTGGCTTGGAAGACCGACGCGATGAAGCCCAGACCTGCAGGGTTCGTGGATAATAAACTCAAG CTGTGGCTTGGAAGACCGACGCGATGAAGCCCGGACCTGCAGGGTTCGTGGATAATAAACTCAAG T C NVL Ensembl:ENSG00000143748 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:224330019..224330119;chr1:224330005..224330125 26863196 MeRIP-seq:(Medium) rs1317948604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1737661,Human_RBP_ID_3298497,Human_RBP_ID_4077168 Human_Splice_Rec_191033,Human_Splice_Rec_191073,Human_Splice_Rec_191115,Human_Splice_Rec_191161,Human_Splice_Rec_191205,Human_Splice_Rec_191247,Human_Splice_Rec_191299,Human_Splice_Rec_191321,Human_Splice_Rec_191333,Human_Splice_Rec_191339,Human_Splice_Rec_191351,Human_Splice_Rec_191363,Human_Splice_Rec_191369,Human_Splice_Rec_191381,Human_Splice_Rec_191393,Human_Splice_Rec_191401,Human_Splice_Rec_191407 RMVar_hsa_circ_88659,RMVar_hsa_circ_139868 102995 RMVar_ID_102995 Human_SNP_ID_51597365 m1A Human chr1 - 224330123 224330123 224330123 CCGAGCTGTGGCTTGGAAGACCGACGCGATGAAGCCCAGACCTGCAGGGTTCGTGGATAATAAAC CCGAGCTGTGGCTTGGAAGACCGACGCGATGACGCCCAGACCTGCAGGGTTCGTGGATAATAAAC T G NVL Ensembl:ENSG00000143748 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:224330040..224330125 26863196 MeRIP-seq:(Medium) rs756422352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1737661,Human_RBP_ID_3298497,Human_RBP_ID_4077168 Human_Splice_Rec_191033,Human_Splice_Rec_191073,Human_Splice_Rec_191115,Human_Splice_Rec_191161,Human_Splice_Rec_191205,Human_Splice_Rec_191247,Human_Splice_Rec_191299,Human_Splice_Rec_191321,Human_Splice_Rec_191333,Human_Splice_Rec_191339,Human_Splice_Rec_191351,Human_Splice_Rec_191363,Human_Splice_Rec_191369,Human_Splice_Rec_191381,Human_Splice_Rec_191393,Human_Splice_Rec_191401,Human_Splice_Rec_191407 RMVar_hsa_circ_88659,RMVar_hsa_circ_139868 102996 RMVar_ID_102996 Human_SNP_ID_51604635 m1A Human chr1 + 224356916 224356913 224356916 AGCGGGTTTGACGGAAGGAGCGGCGGCGACGGAGGAGGAGGATGGAGGCGGTGGTGTTCGTCTTC AGCGGGTTTGACGGAAGGAGCGGCGGCGAC___GGAGGAGGATGGAGGCGGTGGTGTTCGTCTTC CGGA C CNIH4 Ensembl:ENSG00000143771 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:224356870..224356941 26863196 MeRIP-seq:(Medium) rs768665444 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_223437,Human_RBP_ID_4073286,Human_RBP_ID_5413562,Human_RBP_ID_8299630,Human_RBP_ID_17338664,Human_RBP_ID_23122178 Human_Splice_Rec_191411,Human_Splice_Rec_191417,Human_Splice_Rec_191423,Human_Splice_Rec_191431,Human_Splice_Rec_191445 102997 RMVar_ID_102997 Human_SNP_ID_51604677 m1A Human chr1 - 224356964 224356964 224356964 TACGAAGTAGACCGAGAGGAAGATGAGCGCGCAACAATCGAGGAGAGAGAAGACGAACACCACCG TACGAAGTAGACCGAGAGGAAGATGAGCGCGCGACAATCGAGGAGAGAGAAGACGAACACCACCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:224356916..224357047;chr1:224356914..224357030 26863196 MeRIP-seq:(Medium) rs776872569 Functional Loss SNV dbSNP153 33..33 33 - - - 102998 RMVar_ID_102998 Human_SNP_ID_51604678 m1A Human chr1 - 224356964 224356964 224356964 TACGAAGTAGACCGAGAGGAAGATGAGCGCGCAACAATCGAGGAGAGAGAAGACGAACACCACCG TACGAAGTAGACCGAGAGGAAGATGAGCGCGCCACAATCGAGGAGAGAGAAGACGAACACCACCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:224356916..224357047;chr1:224356914..224357030 26863196 MeRIP-seq:(Medium) rs776872569 Functional Loss SNV dbSNP153 33..33 33 - - - 102999 RMVar_ID_102999 Human_SNP_ID_51609166 m1A Human chr1 + 224375831 224375831 224375831 ATCTTAGCTTTGATAAATGACTGAAGCTGGAGAAGCCGTGGTTGAAGTCAGCCTACACTACAGTG ATCTTAGCTTTGATAAATGACTGAAGCTGGAGGAGCCGTGGTTGAAGTCAGCCTACACTACAGTG A G CNIH4 Ensembl:ENSG00000143771 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs202001860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_342956,Human_RBP_ID_860755,Human_RBP_ID_1421787,Human_RBP_ID_1737672,Human_RBP_ID_3298513,Human_RBP_ID_8299648,Human_RBP_ID_8963534,Human_RBP_ID_10796028,Human_RBP_ID_17222036,Human_RBP_ID_17647216,Human_RBP_ID_18563946,Human_RBP_ID_22431279,Human_RBP_ID_23366943,Human_RBP_ID_26799499,Human_RBP_ID_27587900 Human_Splice_Rec_191422,Human_Splice_Rec_191430,Human_Splice_Rec_191438,Human_Splice_Rec_191444 RMVar_hsa_circ_139876,RMVar_hsa_circ_124045,RMVar_hsa_circ_139879,RMVar_hsa_circ_139874,RMVar_hsa_circ_139875,RMVar_hsa_circ_82289 103000 RMVar_ID_103000 Human_SNP_ID_51618007 m1A Human chr1 - 224411784 224411784 224411784 GGAGAGTCTCTTGACCCCAGGCGGTCAGGGCTACAGTGATCTATGATTGTGCTACTGTACAACAG GGAGAGTCTCTTGACCCCAGGCGGTCAGGGCTGCAGTGATCTATGATTGTGCTACTGTACAACAG T C WDR26 Ensembl:ENSG00000162923 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs970173072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558110 RMVar_hsa_circ_6805,RMVar_hsa_circ_44224,RMVar_hsa_circ_119423,RMVar_hsa_circ_340235,RMVar_hsa_circ_354059,RMVar_hsa_circ_315235,RMVar_hsa_circ_139882,RMVar_hsa_circ_4093,RMVar_hsa_circ_57943,RMVar_hsa_circ_139880,RMVar_hsa_circ_139881,RMVar_hsa_circ_300897,RMVar_hsa_circ_61902,RMVar_hsa_circ_27780,RMVar_hsa_circ_105633,RMVar_hsa_circ_91491,RMVar_hsa_circ_139888,RMVar_hsa_circ_139889,RMVar_hsa_circ_373930,RMVar_hsa_circ_26004,RMVar_hsa_circ_139891,RMVar_hsa_circ_64892,RMVar_hsa_circ_357811,RMVar_hsa_circ_301018,RMVar_hsa_circ_139896,RMVar_hsa_circ_139892,RMVar_hsa_circ_364188,RMVar_hsa_circ_33677,RMVar_hsa_circ_325470,RMVar_hsa_circ_29261,RMVar_hsa_circ_282823,RMVar_hsa_circ_28085,RMVar_hsa_circ_271569,RMVar_hsa_circ_139893,RMVar_hsa_circ_139894,RMVar_hsa_circ_282848,RMVar_hsa_circ_288757,RMVar_hsa_circ_365120,RMVar_hsa_circ_281646,RMVar_hsa_circ_139898,RMVar_hsa_circ_139899,RMVar_hsa_circ_139897 103001 RMVar_ID_103001 Human_SNP_ID_51623715 m1A Human chr1 - 224434268 224434268 224434268 GCGGAGGGAGTAGGAGAGCCCGGGGCTTCGGCAGGCAGAGCAGGCCTCTCCCCTCCGTCCTCGTC GCGGAGGGAGTAGGAGAGCCCGGGGCTTCGGCCGGCAGAGCAGGCCTCTCCCCTCCGTCCTCGTC T G WDR26 Ensembl:ENSG00000162923 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224433738..224435755 26863196 MeRIP-seq:(Medium) rs1047695684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_343095,Human_RBP_ID_26774700,Human_RBP_ID_26854144,Human_RBP_ID_27394347 RMVar_hsa_circ_95509,RMVar_hsa_circ_139903 103002 RMVar_ID_103002 Human_SNP_ID_51623810 m1A Human chr1 + 224434541 224434541 224434541 GTGAGGGTGAGGGTGAGAGGAGGGGGAGGAGGAGGAGGGGGAGAAGGAGGATCCGGGCCCTTTCC GTGAGGGTGAGGGTGAGAGGAGGGGGAGGAGGGGGAGGGGGAGAAGGAGGATCCGGGCCCTTTCC A G lnc-CNIH3-2 RNACentral:URS00008C0E46 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:224434491..224434633 32194978 MeRIP-seq:(Medium) rs1274588979 Functional Loss SNV dbSNP153 33..33 33 - - - 103003 RMVar_ID_103003 Human_SNP_ID_51623822 m1A Human chr1 - 224434569 224434568 224434569 ACCCCGAGCTGCCTCCGGGAGGGGGGGGGGAAAGGGCCCGGATCCTCCTTCTCCCCCTCCTCCTC ACCCCGAGCTGCCTCCGGGAGGGGGGGGGGAA_GGGCCCGGATCCTCCTTCTCCCCCTCCTCCTC CT C WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:224434398..224434752 26863410 MeRIP-seq:(Medium) rs992577268 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5125339,Human_RBP_ID_9320363,Human_RBP_ID_18930425,Human_RBP_ID_22026554,Human_RBP_ID_22429990,Human_RBP_ID_26774701 103004 RMVar_ID_103004 Human_SNP_ID_51623824 m1A Human chr1 - 224434571 224434571 224434571 GCACCCCGAGCTGCCTCCGGGAGGGGGGGGGGAAAGGGCCCGGATCCTCCTTCTCCCCCTCCTCC GCACCCCGAGCTGCCTCCGGGAGGGGGGGGGGGAAGGGCCCGGATCCTCCTTCTCCCCCTCCTCC T C WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:224434251..224434710 26863410 MeRIP-seq:(Medium) rs1280227705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125339,Human_RBP_ID_9320363,Human_RBP_ID_18930425,Human_RBP_ID_22026554,Human_RBP_ID_22429990,Human_RBP_ID_26774701 103005 RMVar_ID_103005 Human_SNP_ID_51623851 m1A Human chr1 - 224434582 224434581 224434582 CCCCGGGCCGCGCACCCCGAGCTGCCTCCGGGAGGGGGGGGGGAAAGGGCCCGGATCCTCCTTCT CCCCGGGCCGCGCACCCCGAGCTGCCTCCGGG_GGGGGGGGGGAAAGGGCCCGGATCCTCCTTCT CT C WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:224434184..224434800 26863410 MeRIP-seq:(Medium) rs1382883473 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5125339,Human_RBP_ID_9320363,Human_RBP_ID_22026554,Human_RBP_ID_22429990 103006 RMVar_ID_103006 Human_SNP_ID_51623855 m1A Human chr1 - 224434582 224434582 224434582 CCCCGGGCCGCGCACCCCGAGCTGCCTCCGGGAGGGGGGGGGGAAAGGGCCCGGATCCTCCTTCT CCCCGGGCCGCGCACCCCGAGCTGCCTCCGGGGGGGGGGGGGGAAAGGGCCCGGATCCTCCTTCT T C WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:224434184..224434800 26863410 MeRIP-seq:(Medium) rs1177491559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125339,Human_RBP_ID_9320363,Human_RBP_ID_22026554,Human_RBP_ID_22429990 103007 RMVar_ID_103007 Human_SNP_ID_51623893 m1A Human chr1 - 224434684 224434684 224434684 CGCTGCCGCCCGCCGCCGCCGCCGCCGCAGCCACTGCCGGGGCTCAGCCCAGCGGCGGGCCCCGC CGCTGCCGCCCGCCGCCGCCGCCGCCGCAGCCCCTGCCGGGGCTCAGCCCAGCGGCGGGCCCCGC T G WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224434637..224434775 26863196 MeRIP-seq:(Medium) rs1222655420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_745484,Human_RBP_ID_4074775,Human_RBP_ID_5125340,Human_RBP_ID_5137772,Human_RBP_ID_18415144,Human_RBP_ID_26312767 103008 RMVar_ID_103008 Human_SNP_ID_51623921 m1A Human chr1 - 224434736 224434736 224434736 ACACCAGGGAGCAGAGCGGAGCGGATCCGAGGACAGAGGCGGCAGCTGCCTCCGCTGCCGCCCGC ACACCAGGGAGCAGAGCGGAGCGGATCCGAGGGCAGAGGCGGCAGCTGCCTCCGCTGCCGCCCGC T C WDR26 Ensembl:ENSG00000162923 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:224434208..224434800 26863196 MeRIP-seq:(Medium) rs970190164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224498,Human_RBP_ID_4076394,Human_RBP_ID_5125340,Human_RBP_ID_5137772,Human_RBP_ID_5537404,Human_RBP_ID_5764522,Human_RBP_ID_17558113,Human_RBP_ID_18415144,Human_RBP_ID_18930426,Human_RBP_ID_22871654,Human_RBP_ID_24556255,Human_RBP_ID_26312767,Human_RBP_ID_27176401 103009 RMVar_ID_103009 Human_SNP_ID_51737168 m1A Human chr1 - 224929724 224929724 224929724 CAGACTAGGGTGAATGGGAAGGACCGCGCAGCACAGCCCTACCACGCCAGGCTCCGACGCCTCCT CAGACTAGGGTGAATGGGAAGGACCGCGCAGCGCAGCCCTACCACGCCAGGCTCCGACGCCTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:224929674..224929886 26863196 MeRIP-seq:(Medium) rs1277187609 Functional Loss SNV dbSNP153 33..33 33 - - - 103010 RMVar_ID_103010 Human_SNP_ID_301286218 m1A Human chr6 + 150069075 150069075 150069075 CGCGGGGCTGGCGGCCGCTGCCATTGTAGACCAGGAGCGCCCGGGACACAAGGCGCAGTCGATGT CGCGGGGCTGGCGGCCGCTGCCATTGTAGACCTGGAGCGCCCGGGACACAAGGCGCAGTCGATGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:150069038..150069188 26863196 MeRIP-seq:(Medium) rs1276419428 Functional Loss SNV dbSNP153 33..33 33 - - - 103011 RMVar_ID_103011 Human_SNP_ID_301305252 m1A Human chr6 + 150143220 150143220 150143220 GGGACATGTCGGTGGCGACGGGCAGCAGCGAGACGGCCGGCGGGGCCAGCGGCGGCGGCGCACGG GGGACATGTCGGTGGCGACGGGCAGCAGCGAGGCGGCCGGCGGGGCCAGCGGCGGCGGCGCACGG A G PPP1R14C Ensembl:ENSG00000198729 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:150143124..150143369 26863410 MeRIP-seq:(Medium) rs2297672 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - 103012 RMVar_ID_103012 Human_SNP_ID_301417585 m1A Human chr6 + 150599949 150599949 150599949 CTGCAGGGCGCTCCGGCAGCCCGAGCCGGCGCAGCGCAGCCCGCACCCTCCCCGCCCGACCTGCG CTGCAGGGCGCTCCGGCAGCCCGAGCCGGCGCCGCGCAGCCCGCACCCTCCCCGCCCGACCTGCG A C PLEKHG1 Ensembl:ENSG00000120278 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:150599899..150600006 26863196 MeRIP-seq:(Medium) rs1562373607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_822613,Human_Splice_Rec_822619,Human_Splice_Rec_822623 103013 RMVar_ID_103013 Human_SNP_ID_301481680 m1A Human chr6 - 150865794 150865794 150865794 CCATGGCGCGGGACGGCTGGTTCTCAGGGGACACGGAGCTGCGGCTGCCGAGGGCGGCGGGGCGC CCATGGCGCGGGACGGCTGGTTCTCAGGGGACGCGGAGCTGCGGCTGCCGAGGGCGGCGGGGCGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:150865746..150865893 26863196 MeRIP-seq:(Medium) rs1471899911 Functional Loss SNV dbSNP153 33..33 33 - - - 103014 RMVar_ID_103014 Human_SNP_ID_301484657 m1A Human chr6 + 150876134 150876133 150876134 GAATTCAAAAGAAGTTCTAAGTTTATTGCAAGAAAAAAACCCTGCCTTCAAGCCGGTTCTTGCAA GAATTCAAAAGAAGTTCTAAGTTTATTGCAAG_AAAAAACCCTGCCTTCAAGCCGGTTCTTGCAA GA G MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs769597461 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2983338,Human_RBP_ID_17305228 Human_Splice_Rec_822726,Human_Splice_Rec_822727,Human_Splice_Rec_822780,Human_Splice_Rec_822781,Human_Splice_Rec_822834,Human_Splice_Rec_822835,Human_Splice_Rec_822848,Human_Splice_Rec_822849,Human_Splice_Rec_822868,Human_Splice_Rec_822869,Human_Splice_Rec_822922,Human_Splice_Rec_822923,Human_Splice_Rec_822942,Human_Splice_Rec_822943 Human_miRNA_ID_2931562 RMVar_hsa_circ_27359,RMVar_hsa_circ_295211,RMVar_hsa_circ_335989,RMVar_hsa_circ_242293,RMVar_hsa_circ_75615,RMVar_hsa_circ_339453,RMVar_hsa_circ_365241,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_296900,RMVar_hsa_circ_47344,RMVar_hsa_circ_294609,RMVar_hsa_circ_36630,RMVar_hsa_circ_242294 103015 RMVar_ID_103015 Human_SNP_ID_301497056 m1A Human chr6 + 150926271 150926271 150926271 GTCCGTGCTAGAAAGGTTAAAGGATCAAGCAGATGGAAAATACGTCTTAGTTGCTGGGTAAGACA GTCCGTGCTAGAAAGGTTAAAGGATCAAGCAGGTGGAAAATACGTCTTAGTTGCTGGGTAAGACA A G MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:150926122..150926272 32194978 MeRIP-seq:(Medium) rs746343699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79938,Human_RBP_ID_9401299,Human_RBP_ID_18856562 Human_Splice_Rec_822745,Human_Splice_Rec_822799,Human_Splice_Rec_822887,Human_Splice_Rec_822939 Human_miRNA_ID_556826,Human_miRNA_ID_559252,Human_miRNA_ID_2198179,Human_miRNA_ID_2198180,Human_miRNA_ID_2198410,Human_miRNA_ID_2198411 RMVar_hsa_circ_761,RMVar_hsa_circ_27359,RMVar_hsa_circ_335989,RMVar_hsa_circ_339453,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_36630,RMVar_hsa_circ_46957,RMVar_hsa_circ_57238,RMVar_hsa_circ_64453,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_17387,RMVar_hsa_circ_291513,RMVar_hsa_circ_242302,RMVar_hsa_circ_301274,RMVar_hsa_circ_99529,RMVar_hsa_circ_242305,RMVar_hsa_circ_330553,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_378680,RMVar_hsa_circ_324855,RMVar_hsa_circ_312007,RMVar_hsa_circ_61258,RMVar_hsa_circ_297911,RMVar_hsa_circ_111201,RMVar_hsa_circ_29523,RMVar_hsa_circ_55339,RMVar_hsa_circ_5728,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242308,RMVar_hsa_circ_242310,RMVar_hsa_circ_242309,RMVar_hsa_circ_242307,RMVar_hsa_circ_38704,RMVar_hsa_circ_342519,RMVar_hsa_circ_360422,RMVar_hsa_circ_343919,RMVar_hsa_circ_49243,RMVar_hsa_circ_302071,RMVar_hsa_circ_74329,RMVar_hsa_circ_242314,RMVar_hsa_circ_14247,RMVar_hsa_circ_42488,RMVar_hsa_circ_3386 103016 RMVar_ID_103016 Human_SNP_ID_301498784 m1A Human chr6 - 150932857 150932854 150932857 TTCCTTCCTTCCTTCTTTCCTTAAGGTAATCTAATTACTCTCTCTCCCTTCCTTCCTTCCTTCCT TTCCTTCCTTCCTTCTTTCCTTAAGGTAATCT___TACTCTCTCTCCCTTCCTTCCTTCCTTCCT AATT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:150932852..150932935 26863196 MeRIP-seq:(Medium) rs1264718747 Functional Loss DEL dbSNP153 33..35 33 - - - 103017 RMVar_ID_103017 Human_SNP_ID_301500642 m1A Human chr6 + 150940404 150940404 150940404 AAAATCGTCCCAGGCCTCAGGTCAGAATGGGGATGGGTACCATTCATGAGCCAGCAAGACCCAGA AAAATCGTCCCAGGCCTCAGGTCAGAATGGGGGTGGGTACCATTCATGAGCCAGCAAGACCCAGA A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:150940401..150940526 26863196 MeRIP-seq:(Medium) rs543485067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_761,RMVar_hsa_circ_335989,RMVar_hsa_circ_339453,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_36630,RMVar_hsa_circ_46957,RMVar_hsa_circ_57238,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_17387,RMVar_hsa_circ_301274,RMVar_hsa_circ_330553,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_61258,RMVar_hsa_circ_297911,RMVar_hsa_circ_111201,RMVar_hsa_circ_29523,RMVar_hsa_circ_55339,RMVar_hsa_circ_5728,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242308,RMVar_hsa_circ_242307,RMVar_hsa_circ_38704,RMVar_hsa_circ_342519,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_74329,RMVar_hsa_circ_6210,RMVar_hsa_circ_3386,RMVar_hsa_circ_265387,RMVar_hsa_circ_346667,RMVar_hsa_circ_374610,RMVar_hsa_circ_284484,RMVar_hsa_circ_25543,RMVar_hsa_circ_242315,RMVar_hsa_circ_242316 103018 RMVar_ID_103018 Human_SNP_ID_301500643 m1A Human chr6 + 150940404 150940404 150940404 AAAATCGTCCCAGGCCTCAGGTCAGAATGGGGATGGGTACCATTCATGAGCCAGCAAGACCCAGA AAAATCGTCCCAGGCCTCAGGTCAGAATGGGGTTGGGTACCATTCATGAGCCAGCAAGACCCAGA A T MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:150940401..150940526 26863196 MeRIP-seq:(Medium) rs543485067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_761,RMVar_hsa_circ_335989,RMVar_hsa_circ_339453,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_36630,RMVar_hsa_circ_46957,RMVar_hsa_circ_57238,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_17387,RMVar_hsa_circ_301274,RMVar_hsa_circ_330553,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_61258,RMVar_hsa_circ_297911,RMVar_hsa_circ_111201,RMVar_hsa_circ_29523,RMVar_hsa_circ_55339,RMVar_hsa_circ_5728,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242308,RMVar_hsa_circ_242307,RMVar_hsa_circ_38704,RMVar_hsa_circ_342519,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_74329,RMVar_hsa_circ_6210,RMVar_hsa_circ_3386,RMVar_hsa_circ_265387,RMVar_hsa_circ_346667,RMVar_hsa_circ_374610,RMVar_hsa_circ_284484,RMVar_hsa_circ_25543,RMVar_hsa_circ_242315,RMVar_hsa_circ_242316 103019 RMVar_ID_103019 Human_SNP_ID_301500913 m1A Human chr6 + 150941513 150941513 150941513 CTCTCAGTAGACACGATGAATCCAGGAGGAAGACTATGGAAGTAGCCTAGGGAAAGATGTCAGTG CTCTCAGTAGACACGATGAATCCAGGAGGAAGGCTATGGAAGTAGCCTAGGGAAAGATGTCAGTG A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:150941494..150941785 26863196 MeRIP-seq:(Medium) rs746304952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15687162 RMVar_hsa_circ_761,RMVar_hsa_circ_335989,RMVar_hsa_circ_339453,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_36630,RMVar_hsa_circ_46957,RMVar_hsa_circ_57238,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_17387,RMVar_hsa_circ_301274,RMVar_hsa_circ_330553,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_61258,RMVar_hsa_circ_297911,RMVar_hsa_circ_111201,RMVar_hsa_circ_29523,RMVar_hsa_circ_55339,RMVar_hsa_circ_5728,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242308,RMVar_hsa_circ_242307,RMVar_hsa_circ_38704,RMVar_hsa_circ_342519,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_74329,RMVar_hsa_circ_6210,RMVar_hsa_circ_3386,RMVar_hsa_circ_265387,RMVar_hsa_circ_346667,RMVar_hsa_circ_374610,RMVar_hsa_circ_284484,RMVar_hsa_circ_25543,RMVar_hsa_circ_242315,RMVar_hsa_circ_242316 103020 RMVar_ID_103020 Human_SNP_ID_301500928 m1A Human chr6 - 150941596 150941596 150941596 TCTAATCCTGCAAACATCAGCAAACAAATCTTAAACTGTTTTTTCCTCTTTTCCATCCTCACTGC TCTAATCCTGCAAACATCAGCAAACAAATCTTGAACTGTTTTTTCCTCTTTTCCATCCTCACTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:150941594..150941706 26863196 MeRIP-seq:(Medium) rs1194970546 Functional Loss SNV dbSNP153 33..33 33 - - - 103021 RMVar_ID_103021 Human_SNP_ID_301504548 m1A Human chr6 - 150956073 150956073 150956073 ACAGAGCCACACCCGGGAAGAAAGCACCACCTACCTGCCGGTAATGGCCCTTCTCTGTGTTTCCC ACAGAGCCACACCCGGGAAGAAAGCACCACCTCCCTGCCGGTAATGGCCCTTCTCTGTGTTTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:150956046..150956125 26863196 MeRIP-seq:(Medium) rs75990776 Functional Loss SNV dbSNP153 33..33 33 - - - 103022 RMVar_ID_103022 Human_SNP_ID_301517766 m1A Human chr6 + 151009900 151009900 151009900 CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCAACGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCACCGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC A C MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:151009849..151009949 32194978 MeRIP-seq:(Medium) rs202154575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9189743,Human_RBP_ID_9401302,Human_RBP_ID_19019123,Human_RBP_ID_22460819 Human_Splice_Rec_822764,Human_Splice_Rec_822765,Human_Splice_Rec_822818,Human_Splice_Rec_822819,Human_Splice_Rec_822906,Human_Splice_Rec_822907,Human_Splice_Rec_822958 RMVar_hsa_circ_335989,RMVar_hsa_circ_36630,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_111201,RMVar_hsa_circ_55339,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242307,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_265387,RMVar_hsa_circ_127783,RMVar_hsa_circ_86612,RMVar_hsa_circ_242330,RMVar_hsa_circ_242317,RMVar_hsa_circ_21076,RMVar_hsa_circ_242318,RMVar_hsa_circ_320188,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387,RMVar_hsa_circ_343288,RMVar_hsa_circ_373401,RMVar_hsa_circ_327786,RMVar_hsa_circ_242328,RMVar_hsa_circ_242329,RMVar_hsa_circ_31693,RMVar_hsa_circ_242333,RMVar_hsa_circ_279033,RMVar_hsa_circ_283935,RMVar_hsa_circ_67375,RMVar_hsa_circ_242332 103023 RMVar_ID_103023 Human_SNP_ID_301517767 m1A Human chr6 + 151009900 151009900 151009900 CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCAACGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCAGCGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC A G MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:151009849..151009949 32194978 MeRIP-seq:(Medium) rs202154575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9189743,Human_RBP_ID_9401302,Human_RBP_ID_19019123,Human_RBP_ID_22460819 Human_Splice_Rec_822764,Human_Splice_Rec_822765,Human_Splice_Rec_822818,Human_Splice_Rec_822819,Human_Splice_Rec_822906,Human_Splice_Rec_822907,Human_Splice_Rec_822958 RMVar_hsa_circ_335989,RMVar_hsa_circ_36630,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_111201,RMVar_hsa_circ_55339,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242307,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_265387,RMVar_hsa_circ_127783,RMVar_hsa_circ_86612,RMVar_hsa_circ_242330,RMVar_hsa_circ_242317,RMVar_hsa_circ_21076,RMVar_hsa_circ_242318,RMVar_hsa_circ_320188,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387,RMVar_hsa_circ_343288,RMVar_hsa_circ_373401,RMVar_hsa_circ_327786,RMVar_hsa_circ_242328,RMVar_hsa_circ_242329,RMVar_hsa_circ_31693,RMVar_hsa_circ_242333,RMVar_hsa_circ_279033,RMVar_hsa_circ_283935,RMVar_hsa_circ_67375,RMVar_hsa_circ_242332 103024 RMVar_ID_103024 Human_SNP_ID_301517768 m1A Human chr6 + 151009900 151009900 151009900 CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCAACGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC CATCAAGTGCCGAGCTTCCGGCTTGGTGCCCATCGTGGTTGTGTTAGTGGCAACGGTGCGAGCTC A T MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:151009849..151009949 32194978 MeRIP-seq:(Medium) rs202154575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9189743,Human_RBP_ID_9401302,Human_RBP_ID_19019123,Human_RBP_ID_22460819 Human_Splice_Rec_822764,Human_Splice_Rec_822765,Human_Splice_Rec_822818,Human_Splice_Rec_822819,Human_Splice_Rec_822906,Human_Splice_Rec_822907,Human_Splice_Rec_822958 RMVar_hsa_circ_335989,RMVar_hsa_circ_36630,RMVar_hsa_circ_85300,RMVar_hsa_circ_242299,RMVar_hsa_circ_355678,RMVar_hsa_circ_372784,RMVar_hsa_circ_111201,RMVar_hsa_circ_55339,RMVar_hsa_circ_9172,RMVar_hsa_circ_242306,RMVar_hsa_circ_242307,RMVar_hsa_circ_360422,RMVar_hsa_circ_49243,RMVar_hsa_circ_265387,RMVar_hsa_circ_127783,RMVar_hsa_circ_86612,RMVar_hsa_circ_242330,RMVar_hsa_circ_242317,RMVar_hsa_circ_21076,RMVar_hsa_circ_242318,RMVar_hsa_circ_320188,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387,RMVar_hsa_circ_343288,RMVar_hsa_circ_373401,RMVar_hsa_circ_327786,RMVar_hsa_circ_242328,RMVar_hsa_circ_242329,RMVar_hsa_circ_31693,RMVar_hsa_circ_242333,RMVar_hsa_circ_279033,RMVar_hsa_circ_283935,RMVar_hsa_circ_67375,RMVar_hsa_circ_242332 103025 RMVar_ID_103025 Human_SNP_ID_301538050 m1A Human chr6 - 151092517 151092517 151092517 AAGCCTTTAACTTGTTCTGTTTCGGTATCAAGATCTATGTCATAAAAGCAGGGCCGGGTGGGCAG AAGCCTTTAACTTGTTCTGTTTCGGTATCAAGTTCTATGTCATAAAAGCAGGGCCGGGTGGGCAG T A AL138733.1 Ensembl:ENSG00000223598 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:151042049..151092551 32194978 MeRIP-seq:(Medium) rs1364225813 Functional Loss SNV dbSNP153 33..33 33 - - - 103026 RMVar_ID_103026 Human_SNP_ID_301604367 m1A Human chr6 + 151348941 151348941 151348941 AGAAGGTGTTTAAGTTTGTTGGCTTTAAATTCACTGTGAAAAAGGATAAGACAGAGAAGCCTGAC AGAAGGTGTTTAAGTTTGTTGGCTTTAAATTCGCTGTGAAAAAGGATAAGACAGAGAAGCCTGAC A G AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:151348891..151349042 32194978 MeRIP-seq:(Medium) rs1227548197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1665799,Human_RBP_ID_2011549,Human_RBP_ID_8897496 Human_miRNA_ID_164019,Human_miRNA_ID_1995162,Human_miRNA_ID_2227658,Human_miRNA_ID_2285175,Human_miRNA_ID_2288174,Human_miRNA_ID_2503636 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 103027 RMVar_ID_103027 Human_SNP_ID_301604523 m1A Human chr6 + 151349387 151349387 151349387 GAAGCTTCAGAGAAGAAAAAGGAACAAGAGCCAGAAAAAGTAGACACAGAAGAAGACGGAAAGGC GAAGCTTCAGAGAAGAAAAAGGAACAAGAGCCGGAAAAAGTAGACACAGAAGAAGACGGAAAGGC A G AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151349336..151349475 26863196 MeRIP-seq:(Medium) rs201823889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1665800,Human_RBP_ID_5617442 Human_miRNA_ID_2082894,Human_miRNA_ID_3114408 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 103028 RMVar_ID_103028 Human_SNP_ID_301604955 m1A Human chr6 + 151350558 151350558 151350558 AGAAAGCTGATGAGGCCGGAAAAGACAAAGAGACGGGGACAGACGGGATCCTTGCTGGTTCCCAA AGAAAGCTGATGAGGCCGGAAAAGACAAAGAGGCGGGGACAGACGGGATCCTTGCTGGTTCCCAA A G AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151350427..151350570 26863196 MeRIP-seq:(Medium) rs1399792327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80184,Human_RBP_ID_841689,Human_RBP_ID_950871,Human_RBP_ID_7560475,Human_RBP_ID_9401306 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 103029 RMVar_ID_103029 Human_SNP_ID_301605199 m1A Human chr6 + 151351206 151351206 151351206 AAGCCGCACTGTTAACTGAGGAGGTATTGGAAAGAGAAGTAATTGCAGAAGAAGAACCCCCCACG AAGCCGCACTGTTAACTGAGGAGGTATTGGAAGGAGAAGTAATTGCAGAAGAAGAACCCCCCACG A G AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151351157..151351404 26863196 MeRIP-seq:(Medium) rs769514807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2011563,Human_RBP_ID_8897534 Human_miRNA_ID_3116907 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 103030 RMVar_ID_103030 Human_SNP_ID_301605220 m1A Human chr6 - 151351252 151351252 151351252 CCGTGTCGCCCCGGGCCTCTCTGTTCTCTGGCAGAGGTTCAGTAACCGTGGGGGGTTCTTCTTCT CCGTGTCGCCCCGGGCCTCTCTGTTCTCTGGCGGAGGTTCAGTAACCGTGGGGGGTTCTTCTTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:151351201..151351326 26863196 MeRIP-seq:(Medium) rs1256368798 Functional Loss SNV dbSNP153 33..33 33 - - - 103031 RMVar_ID_103031 Human_SNP_ID_301605344 m1A Human chr6 - 151351519 151351519 151351519 ATTCCTCTTTCACTTTTTCTGCCACTGCCTGGAGGACCTCTTGAGTCCGCCTCTCTTGCTCTTCT ATTCCTCTTTCACTTTTTCTGCCACTGCCTGGCGGACCTCTTGAGTCCGCCTCTCTTGCTCTTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151351469..151351689 26863196 MeRIP-seq:(Medium) rs758214075 Functional Loss SNV dbSNP153 33..33 33 - - - 103032 RMVar_ID_103032 Human_SNP_ID_301605345 m1A Human chr6 + 151351522 151351522 151351522 AGAGCAAGAGAGGCGGACTCAAGAGGTCCTCCAGGCAGTGGCAGAAAAAGTGAAAGAGGAATCCC AGAGCAAGAGAGGCGGACTCAAGAGGTCCTCCGGGCAGTGGCAGAAAAAGTGAAAGAGGAATCCC A G AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:151351472..151351622 26863196 MeRIP-seq:(Medium) rs1411711744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1045109 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 103033 RMVar_ID_103033 Human_SNP_ID_301605679 m1A Human chr6 + 151352396 151352396 151352396 CACGCTAAGTCTCCTCCATCCCCCGTGGAGAGAGAGATGGTAGTTCAAGTCGAAAGGGAGAAAAC CACGCTAAGTCTCCTCCATCCCCCGTGGAGAGCGAGATGGTAGTTCAAGTCGAAAGGGAGAAAAC A C AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:151352347..151352441 26863196 MeRIP-seq:(Medium) rs899420451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951769,Human_RBP_ID_18856693 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242341,RMVar_hsa_circ_242337 103034 RMVar_ID_103034 Human_SNP_ID_301613197 m1A Human chr6 - 151380755 151380755 151380755 GCGCAGAGGAGACCAGCAAGTGGAACCCCTGGATGGGGATTAAAATAGAACAGCCTGTGGTGAGT GCGCAGAGGAGACCAGCAAGTGGAACCCCTGGGTGGGGATTAAAATAGAACAGCCTGTGGTGAGT T C ZBTB2 Ensembl:ENSG00000181472 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151380753..151380871 26863196 MeRIP-seq:(Medium) rs986633831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 103035 RMVar_ID_103035 Human_SNP_ID_301616192 m1A Human chr6 + 151391080 151391080 151391080 CCCTCTCGGCTTCCGTCCCCTCCCCCTCCCACAAAACCCCGGATGGAGGCGCCGCCGACTCGCCG CCCTCTCGGCTTCCGTCCCCTCCCCCTCCCACGAAACCCCGGATGGAGGCGCCGCCGACTCGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151391074..151391293 26863196 MeRIP-seq:(Medium) rs1404474520 Functional Loss SNV dbSNP153 33..33 33 - - - 103036 RMVar_ID_103036 Human_SNP_ID_301616204 m1A Human chr6 - 151391107 151391107 151391107 ACAAAACCATCCCCCGGAGCCAGGCGGCGGCGAGTCGGCGGCGCCTCCATCCGGGGTTTTGTGGG ACAAAACCATCCCCCGGAGCCAGGCGGCGGCGTGTCGGCGGCGCCTCCATCCGGGGTTTTGTGGG T A ZBTB2 Ensembl:ENSG00000181472 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151391092..151391297 26863196 MeRIP-seq:(Medium) rs1255436373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 103037 RMVar_ID_103037 Human_SNP_ID_301616230 m1A Human chr6 + 151391151 151391151 151391151 GGCTCCGGGGGATGGTTTTGTCAAGCGGCCAGAGCCCCGGCGCCAGGCGCAGCCGCCGCCGCCCC GGCTCCGGGGGATGGTTTTGTCAAGCGGCCAGTGCCCCGGCGCCAGGCGCAGCCGCCGCCGCCCC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:151391101..151391410 26863196 MeRIP-seq:(Medium) rs1219786299 Functional Loss SNV dbSNP153 33..33 33 - - - 103038 RMVar_ID_103038 Human_SNP_ID_301616355 m1A Human chr6 - 151391430 151391430 151391430 GGCGCCTCCTCCACACCCCCCGCCGCAGCAGCACCGGCGACAGGTAAGCGCGCACCGCCTCCGCC GGCGCCTCCTCCACACCCCCCGCCGCAGCAGCTCCGGCGACAGGTAAGCGCGCACCGCCTCCGCC T A ZBTB2 Ensembl:ENSG00000181472 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:151391409..151391493 26863196 MeRIP-seq:(Medium) rs1490885221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_823003 RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 103039 RMVar_ID_103039 Human_SNP_ID_301616378 m1A Human chr6 + 151391470 151391470 151391470 CGGCGGGGGGTGTGGAGGAGGCGCCTCTGGGCAGCCTCGGCCGTGCTGTCCTCCCCGCCGCCGCC CGGCGGGGGGTGTGGAGGAGGCGCCTCTGGGCGGCCTCGGCCGTGCTGTCCTCCCCGCCGCCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151391387..151391529 26863196 MeRIP-seq:(Medium) rs1203645591 Functional Loss SNV dbSNP153 33..33 33 - - - 103040 RMVar_ID_103040 Human_SNP_ID_301616440 m1A Human chr6 - 151391548 151391548 151391548 CCCGCCGCCGCCGCCGCCGCCGCGCCGGAGACACCGACCGCGGCGGCAGCAGCAGCAGCAGCAGC CCCGCCGCCGCCGCCGCCGCCGCGCCGGAGACTCCGACCGCGGCGGCAGCAGCAGCAGCAGCAGC T A ZBTB2 Ensembl:ENSG00000181472 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151391369..151391603 26863196 MeRIP-seq:(Medium) rs973118740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4869669 103041 RMVar_ID_103041 Human_SNP_ID_301632120 m1A Human chr6 + 151448216 151448216 151448216 ACAGGGCCCTATTGTCATTATCAATACATCGGACCTCCTCATCTCAGTTTCATCCATTTTACTCT ACAGGGCCCTATTGTCATTATCAATACATCGGTCCTCCTCATCTCAGTTTCATCCATTTTACTCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151448214..151448462 26863196 MeRIP-seq:(Medium) rs1475006565 Functional Loss SNV dbSNP153 33..33 33 - - - 103042 RMVar_ID_103042 Human_SNP_ID_301632553 m1A Human chr6 + 151449551 151449551 151449551 TTCTCCCAGGGATCTGAAAGGCTCACACCCTCACCTCCTTCAGATGTTTGCTAAAATGTCTTCTA TTCTCCCAGGGATCTGAAAGGCTCACACCCTCGCCTCCTTCAGATGTTTGCTAAAATGTCTTCTA A G lnc-ARMT1-2 RNACentral:URS0000D5BAA2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:151449524..151449628 26863196 MeRIP-seq:(Medium) rs1238287432 Functional Loss SNV dbSNP153 33..33 33 - - - 103043 RMVar_ID_103043 Human_SNP_ID_301632562 m1A Human chr6 + 151449571 151449571 151449571 GCTCACACCCTCACCTCCTTCAGATGTTTGCTAAAATGTCTTCTACCCAGTGAAGCCTTCCCCAA GCTCACACCCTCACCTCCTTCAGATGTTTGCTGAAATGTCTTCTACCCAGTGAAGCCTTCCCCAA A G lnc-ARMT1-2 RNACentral:URS0000D5BAA2 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151449409..151449619 26863196 MeRIP-seq:(Medium) rs1436979702 Functional Loss SNV dbSNP153 33..33 33 - - - 103044 RMVar_ID_103044 Human_SNP_ID_301633790 m1A Human chr6 + 151452067 151452067 151452067 AAGGAAGCGCCAGGGACGCACGCTTCCTCGGCAGGACTGCAGGGAAAGAGCCGCACCCCCAGCCT AAGGAAGCGCCAGGGACGCACGCTTCCTCGGCTGGACTGCAGGGAAAGAGCCGCACCCCCAGCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151451983..151452103 26863196 MeRIP-seq:(Medium) rs997902308 Functional Loss SNV dbSNP153 33..33 33 - - - 103045 RMVar_ID_103045 Human_SNP_ID_301635780 m1A Human chr6 + 151458452 151458452 151458452 GAAATTTGTTGATACTGATATATGGAATCAGTACCTAGAATATCAACAGAGTCTTTTAAATGAAA GAAATTTGTTGATACTGATATATGGAATCAGTTCCTAGAATATCAACAGAGTCTTTTAAATGAAA A T ARMT1 Ensembl:ENSG00000146476 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:151458402..151458497 32194978 MeRIP-seq:(Medium) rs766575308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1665864,Human_RBP_ID_2011672,Human_RBP_ID_18856740 RMVar_hsa_circ_59950,RMVar_hsa_circ_121276,RMVar_hsa_circ_242359 103046 RMVar_ID_103046 Human_SNP_ID_301637518 m1A Human chr6 - 151465408 151465408 151465408 CAGCCTCCATGGACCCTTCCCTGGCAGCCCTGATCCCTTCTCCAACATTCCCAACGCCCTTTTCC CAGCCTCCATGGACCCTTCCCTGGCAGCCCTGTTCCCTTCTCCAACATTCCCAACGCCCTTTTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151465362..151465549 26863196 MeRIP-seq:(Medium) rs1341263687 Functional Loss SNV dbSNP153 33..33 33 - - - 103047 RMVar_ID_103047 Human_SNP_ID_301638476 m1A Human chr6 + 151469028 151469028 151469028 AGCTGAAATTCAGGTTGGTCTGCAGCCTGGGCAAGGGGAACAGCTCCTGGCCTCTGAGCCCAGCT AGCTGAAATTCAGGTTGGTCTGCAGCCTGGGCGAGGGGAACAGCTCCTGGCCTCTGAGCCCAGCT A G ARMT1 Ensembl:ENSG00000146476 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs765653105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7660271,Human_RBP_ID_8897652 Human_miRNA_ID_2291609,Human_miRNA_ID_2356952,Human_miRNA_ID_2992714,Human_miRNA_ID_3059394 RMVar_hsa_circ_121276,RMVar_hsa_circ_242359 103048 RMVar_ID_103048 Human_SNP_ID_301709305 m1A Human chr6 - 151763950 151763950 151763950 GGCCGCCCTTCCCCTTCCCAGCCCCCTAACTTACCTGTCGCCCTGTCATCCTCCAGGCATCACTC GGCCGCCCTTCCCCTTCCCAGCCCCCTAACTTGCCTGTCGCCCTGTCATCCTCCAGGCATCACTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:151763626..151764090 26863196 MeRIP-seq:(Medium) rs530277891 Functional Loss SNV dbSNP153 33..33 33 - - - 103049 RMVar_ID_103049 Human_SNP_ID_301709422 m1A Human chr6 + 151764432 151764432 151764432 TTTTACTTTGGAGAAGGACTGCCTCAGCCGCGAAAGACCAAGGGGTGGCACCACAGGGAGAAGTC TTTTACTTTGGAGAAGGACTGCCTCAGCCGCGGAAGACCAAGGGGTGGCACCACAGGGAGAAGTC A G ESR1 Ensembl:ENSG00000091831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151764384..151764543 26863196 MeRIP-seq:(Medium) rs952224443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357284,RMVar_hsa_circ_360120,RMVar_hsa_circ_75119,RMVar_hsa_circ_60993 103050 RMVar_ID_103050 Human_SNP_ID_301709423 m1A Human chr6 + 151764432 151764432 151764432 TTTTACTTTGGAGAAGGACTGCCTCAGCCGCGAAAGACCAAGGGGTGGCACCACAGGGAGAAGTC TTTTACTTTGGAGAAGGACTGCCTCAGCCGCGTAAGACCAAGGGGTGGCACCACAGGGAGAAGTC A T ESR1 Ensembl:ENSG00000091831 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:151764384..151764543 26863196 MeRIP-seq:(Medium) rs952224443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357284,RMVar_hsa_circ_360120,RMVar_hsa_circ_75119,RMVar_hsa_circ_60993 103051 RMVar_ID_103051 Human_SNP_ID_301709427 m1A Human chr6 + 151764449 151764449 151764449 ACTGCCTCAGCCGCGAAAGACCAAGGGGTGGCACCACAGGGAGAAGTCTGCACTGCGCTTGTCAG ACTGCCTCAGCCGCGAAAGACCAAGGGGTGGCCCCACAGGGAGAAGTCTGCACTGCGCTTGTCAG A C ESR1 Ensembl:ENSG00000091831 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:151764278..151764534;chr6:151764287..151764542 26863196 MeRIP-seq:(Medium) rs1266925100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357284,RMVar_hsa_circ_360120,RMVar_hsa_circ_75119,RMVar_hsa_circ_60993 103052 RMVar_ID_103052 Human_SNP_ID_301920895 m1A Human chr6 + 152629561 152629559 152629561 GGGGGGGGGAGGGGGAGGGGAGGAGGGGGTGCAGTGGGCTTTGGGAAGAGGTAGGAGAGTAGTCG GGGGGGGGGAGGGGGAGGGGAGGAGGGGGTG__GTGGGCTTTGGGAAGAGGTAGGAGAGTAGTCG GCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:152629434..152629560 26863196 MeRIP-seq:(Medium) rs1202456380 Functional Loss DEL dbSNP153 32..33 33 - - - 103053 RMVar_ID_103053 Human_SNP_ID_301920897 m1A Human chr6 + 152629561 152629561 152629561 GGGGGGGGGAGGGGGAGGGGAGGAGGGGGTGCAGTGGGCTTTGGGAAGAGGTAGGAGAGTAGTCG GGGGGGGGGAGGGGGAGGGGAGGAGGGGGTGCGGTGGGCTTTGGGAAGAGGTAGGAGAGTAGTCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:152629434..152629560 26863196 MeRIP-seq:(Medium) rs1490509599 Functional Loss SNV dbSNP153 33..33 33 - - - 103054 RMVar_ID_103054 Human_SNP_ID_302076659 m1A Human chr6 - 153267683 153267683 153267683 AATAAGTGCATGGCAGAGACACCAAAAGAGCTAAAAAAAAAAAAAAAAAAAAAAAAGCACATGGC AATAAGTGCATGGCAGAGACACCAAAAGAGCTTAAAAAAAAAAAAAAAAAAAAAAAGCACATGGC T A - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs943574729 Functional Loss SNV dbSNP153 33..33 33 - - - 103055 RMVar_ID_103055 Human_SNP_ID_302080419 m1A Human chr6 + 153282727 153282727 153282727 GCCCCTAAGTTTCCGGGTCTTCCTCAGTCTGGATGGCATGTTGGCAGCCCAGACGAAAAAAAAAA GCCCCTAAGTTTCCGGGTCTTCCTCAGTCTGGGTGGCATGTTGGCAGCCCAGACGAAAAAAAAAA A G AL590867.1 Ensembl:ENSG00000213121 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:153282626..153282739 26863410 MeRIP-seq:(Medium) rs1167796338 Functional Loss SNV dbSNP153 33..33 33 - - - 103056 RMVar_ID_103056 Human_SNP_ID_302080420 m1A Human chr6 + 153282727 153282727 153282727 GCCCCTAAGTTTCCGGGTCTTCCTCAGTCTGGATGGCATGTTGGCAGCCCAGACGAAAAAAAAAA GCCCCTAAGTTTCCGGGTCTTCCTCAGTCTGGTTGGCATGTTGGCAGCCCAGACGAAAAAAAAAA A T AL590867.1 Ensembl:ENSG00000213121 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:153282626..153282739 26863410 MeRIP-seq:(Medium) rs1167796338 Functional Loss SNV dbSNP153 33..33 33 - - - 103057 RMVar_ID_103057 Human_SNP_ID_302382705 m1A Human chr6 - 154510530 154510530 154510530 GGACGCCAGCGCACGCGGAGCGGGGACCCCGGAGAGCCAGCAGGCGAGAAGACCGGCCGAGGGAG GGACGCCAGCGCACGCGGAGCGGGGACCCCGGGGAGCCAGCAGGCGAGAAGACCGGCCGAGGGAG T C CNKSR3 Ensembl:ENSG00000153721 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:154510115..154510657;chr6:154510142..154510638;chr6:154510104..154510650 26863196 MeRIP-seq:(Medium) rs535526862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903562,Human_RBP_ID_18425511 103058 RMVar_ID_103058 Human_SNP_ID_302382706 m1A Human chr6 - 154510530 154510530 154510530 GGACGCCAGCGCACGCGGAGCGGGGACCCCGGAGAGCCAGCAGGCGAGAAGACCGGCCGAGGGAG GGACGCCAGCGCACGCGGAGCGGGGACCCCGGCGAGCCAGCAGGCGAGAAGACCGGCCGAGGGAG T G CNKSR3 Ensembl:ENSG00000153721 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:154510115..154510657;chr6:154510142..154510638;chr6:154510104..154510650 26863196 MeRIP-seq:(Medium) rs535526862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903562,Human_RBP_ID_18425511 103059 RMVar_ID_103059 Human_SNP_ID_302382717 m1A Human chr6 - 154510550 154510550 154510550 CCTGCGCCGGGAAGGCTCCGGGACGCCAGCGCACGCGGAGCGGGGACCCCGGAGAGCCAGCAGGC CCTGCGCCGGGAAGGCTCCGGGACGCCAGCGCCCGCGGAGCGGGGACCCCGGAGAGCCAGCAGGC T G CNKSR3 Ensembl:ENSG00000153721 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:154510500..154510614 26863196 MeRIP-seq:(Medium) rs1185633977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903562,Human_RBP_ID_18425511 103060 RMVar_ID_103060 Human_SNP_ID_302382755 m1A Human chr6 + 154510632 154510632 154510632 CCCTCCCGTGCCGCCCTGGCAGGGCCGAGCGCAGAGCGTGCGCGCTCGGGTTGCAAAGTTTCAGC CCCTCCCGTGCCGCCCTGGCAGGGCCGAGCGCGGAGCGTGCGCGCTCGGGTTGCAAAGTTTCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:154510140..154510675 26863196 MeRIP-seq:(Medium) rs1013219396 Functional Loss SNV dbSNP153 33..33 33 - - - 103061 RMVar_ID_103061 Human_SNP_ID_302439608 m1A Human chr6 + 154733468 154733468 154733468 TGCTGCCAGCGCTTCCTCCTCTGTCTTCGCCGAGCGGGGCTGGTTCCTGCGGCCCGAGCGGCGGG TGCTGCCAGCGCTTCCTCCTCTGTCTTCGCCGGGCGGGGCTGGTTCCTGCGGCCCGAGCGGCGGG A G SCAF8 Ensembl:ENSG00000213079 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:154733424..154733940 26863196 MeRIP-seq:(Medium) rs1199971214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251801,Human_RBP_ID_655810,Human_RBP_ID_1665985,Human_RBP_ID_4903563,Human_RBP_ID_5427988,Human_RBP_ID_8905546,Human_RBP_ID_9309441,Human_RBP_ID_18425515,Human_RBP_ID_18472158,Human_RBP_ID_22105466,Human_RBP_ID_23067647,Human_RBP_ID_26354517,Human_RBP_ID_27828110 Human_Splice_Rec_826379,Human_Splice_Rec_826389,Human_Splice_Rec_826427 RMVar_hsa_circ_242463,RMVar_hsa_circ_109480,RMVar_hsa_circ_111572,RMVar_hsa_circ_101214,RMVar_hsa_circ_242464,RMVar_hsa_circ_242462 103062 RMVar_ID_103062 Human_SNP_ID_302439653 m1A Human chr6 + 154733534 154733534 154733534 AGGTGAAACAGGAGCCCGTCGGAGGAAGGGGCAGAAGGGAGTGGAGAGTGTAGGGGAAGGGGCTA AGGTGAAACAGGAGCCCGTCGGAGGAAGGGGCGGAAGGGAGTGGAGAGTGTAGGGGAAGGGGCTA A G SCAF8 Ensembl:ENSG00000213079 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:154733426..154733923 26863196 MeRIP-seq:(Medium) rs916967629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5152801,Human_RBP_ID_8944039 Human_Splice_Rec_826389 RMVar_hsa_circ_242463,RMVar_hsa_circ_109480,RMVar_hsa_circ_111572,RMVar_hsa_circ_101214,RMVar_hsa_circ_242464,RMVar_hsa_circ_242462 103063 RMVar_ID_103063 Human_SNP_ID_302439666 m1A Human chr6 + 154733553 154733553 154733553 CGGAGGAAGGGGCAGAAGGGAGTGGAGAGTGTAGGGGAAGGGGCTAGAGGGAGGGGGACCGAAAC CGGAGGAAGGGGCAGAAGGGAGTGGAGAGTGTCGGGGAAGGGGCTAGAGGGAGGGGGACCGAAAC A C SCAF8 Ensembl:ENSG00000213079 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:154733427..154733600 26863196 MeRIP-seq:(Medium) rs1237086264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5152801,Human_RBP_ID_5510706,Human_RBP_ID_7561973,Human_RBP_ID_8897723,Human_RBP_ID_8944039,Human_RBP_ID_24554673,Human_RBP_ID_26043975 RMVar_hsa_circ_242463,RMVar_hsa_circ_109480,RMVar_hsa_circ_111572,RMVar_hsa_circ_101214,RMVar_hsa_circ_242464,RMVar_hsa_circ_242462 103064 RMVar_ID_103064 Human_SNP_ID_302439783 m1A Human chr6 - 154733805 154733803 154733805 GAGAGCGAGACGCGGGCTGCTGCGTGGCCGCGAGGAGGGGGCGCTGGCGGGAGAGCGGGCCGCTG GAGAGCGAGACGCGGGCTGCTGCGTGGCCGCG__GAGGGGGCGCTGGCGGGAGAGCGGGCCGCTG CCT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:154733700..154733885 26863196 MeRIP-seq:(Medium) rs1211116450 Functional Loss DEL dbSNP153 33..34 33 - - - 103065 RMVar_ID_103065 Human_SNP_ID_302444535 m1A Human chr6 + 154749910 154749910 154749910 TGGGATAGGAAGGTTAAATTAGTCTAGAGAGGATGAGGGGCTCAATTAAAGTAATACTAATAGGG TGGGATAGGAAGGTTAAATTAGTCTAGAGAGGGTGAGGGGCTCAATTAAAGTAATACTAATAGGG A G SCAF8 Ensembl:ENSG00000213079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:154749889..154749991 26863196 MeRIP-seq:(Medium) rs980377702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7562224,Human_RBP_ID_15695999,Human_RBP_ID_24142246 RMVar_hsa_circ_99944,RMVar_hsa_circ_242463,RMVar_hsa_circ_109480,RMVar_hsa_circ_111572,RMVar_hsa_circ_101214,RMVar_hsa_circ_242464,RMVar_hsa_circ_80203,RMVar_hsa_circ_242462,RMVar_hsa_circ_306121,RMVar_hsa_circ_242465,RMVar_hsa_circ_108288,RMVar_hsa_circ_242467,RMVar_hsa_circ_242469,RMVar_hsa_circ_98611,RMVar_hsa_circ_242468,RMVar_hsa_circ_242466 103066 RMVar_ID_103066 Human_SNP_ID_302444536 m1A Human chr6 + 154749910 154749910 154749910 TGGGATAGGAAGGTTAAATTAGTCTAGAGAGGATGAGGGGCTCAATTAAAGTAATACTAATAGGG TGGGATAGGAAGGTTAAATTAGTCTAGAGAGGTTGAGGGGCTCAATTAAAGTAATACTAATAGGG A T SCAF8 Ensembl:ENSG00000213079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:154749889..154749991 26863196 MeRIP-seq:(Medium) rs980377702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7562224,Human_RBP_ID_15695999,Human_RBP_ID_24142246 RMVar_hsa_circ_99944,RMVar_hsa_circ_242463,RMVar_hsa_circ_109480,RMVar_hsa_circ_111572,RMVar_hsa_circ_101214,RMVar_hsa_circ_242464,RMVar_hsa_circ_80203,RMVar_hsa_circ_242462,RMVar_hsa_circ_306121,RMVar_hsa_circ_242465,RMVar_hsa_circ_108288,RMVar_hsa_circ_242467,RMVar_hsa_circ_242469,RMVar_hsa_circ_98611,RMVar_hsa_circ_242468,RMVar_hsa_circ_242466 103067 RMVar_ID_103067 Human_SNP_ID_302451055 m1A Human chr6 - 154773937 154773937 154773937 TTTACATACAGCAAAACTCTCCAAGCAATTACATGAAACTACCAAACATGTTCATTTTTATATTC TTTACATACAGCAAAACTCTCCAAGCAATTACGTGAAACTACCAAACATGTTCATTTTTATATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:154773934..154774009 26863196 MeRIP-seq:(Medium) rs1278160204 Functional Loss SNV dbSNP153 33..33 33 - - - 103068 RMVar_ID_103068 Human_SNP_ID_302589864 m1A Human chr6 - 155311217 155311217 155311217 ATGCCGACGTCGCTGAACTTCTGGTGGTTGAAAAGGACACTCGATTTATTCCTGGATTACAGGTG ATGCCGACGTCGCTGAACTTCTGGTGGTTGAAGAGGACACTCGATTTATTCCTGGATTACAGGTG T C TFB1M Ensembl:ENSG00000029639 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:155311215..155311341 26863196 MeRIP-seq:(Medium) rs1373077919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2012242,Human_RBP_ID_9402877,Human_RBP_ID_19129845 Human_Splice_Rec_826853,Human_Splice_Rec_826893 RMVar_hsa_circ_288758,RMVar_hsa_circ_335906,RMVar_hsa_circ_349813 103069 RMVar_ID_103069 Human_SNP_ID_302590687 m1A Human chr6 - 155314404 155314404 155314404 CGCGTATCATGGCTGCCTCCGGAAAACTCAGCACTTGCCGTCTCCCTCCGTTGCCCACGATTCGA CGCGTATCATGGCTGCCTCCGGAAAACTCAGCGCTTGCCGTCTCCCTCCGTTGCCCACGATTCGA T C TFB1M Ensembl:ENSG00000029639 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:155314353..155314451 26863196 MeRIP-seq:(Medium) rs1562433996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18857160,Human_RBP_ID_22106588,Human_RBP_ID_22462266,Human_RBP_ID_25978054,Human_RBP_ID_27090120 103070 RMVar_ID_103070 Human_SNP_ID_302590721 m1A Human chr6 + 155314440 155314440 155314440 GAGTTTTCCGGAGGCAGCCATGATACGCGGCAAGCACCATCCAACCCTACCTCACCCAGGACCTT GAGTTTTCCGGAGGCAGCCATGATACGCGGCAGGCACCATCCAACCCTACCTCACCCAGGACCTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:155314334..155314463 26863196 MeRIP-seq:(Medium) rs1290757629 Functional Loss SNV dbSNP153 33..33 33 - - - 103071 RMVar_ID_103071 Human_SNP_ID_302590727 m1A Human chr6 + 155314443 155314443 155314443 TTTTCCGGAGGCAGCCATGATACGCGGCAAGCACCATCCAACCCTACCTCACCCAGGACCTTCAC TTTTCCGGAGGCAGCCATGATACGCGGCAAGCCCCATCCAACCCTACCTCACCCAGGACCTTCAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:155314358..155314454 26863196 MeRIP-seq:(Medium) rs774531191 Functional Loss SNV dbSNP153 33..33 33 - - - 103072 RMVar_ID_103072 Human_SNP_ID_302953823 m1A Human chr6 + 156778204 156778178 156778205 CCAGCAGCACCACCACCACCACCATGCCCACCACCACCACCACCATGCCCACCACCTCCACCACC CCAGCAG___________________________CACCACCACCATGCCCACCACCTCCACCACC GCACCACCACCACCACCATGCCCACCAC G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156777818..156778491 26863196 MeRIP-seq:(Medium) rs1234893556 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_26533258 Human_miRNA_ID_2492758,Human_miRNA_ID_2872918,Human_miRNA_ID_2872919,Human_miRNA_ID_2980883,Human_miRNA_ID_2980884 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103073 RMVar_ID_103073 Human_SNP_ID_302953824 m1A Human chr6 + 156778204 156778178 156778205 CCAGCAGCACCACCACCACCACCATGCCCACCACCACCACCACCATGCCCACCACCTCCACCACC CCAGCAGCAC________________________CACCACCACCATGCCCACCACCTCCACCACC GCACCACCACCACCACCATGCCCACCAC GCAC ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156777818..156778491 26863196 MeRIP-seq:(Medium) rs1234893556 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_26533258 Human_miRNA_ID_2492758,Human_miRNA_ID_2872918,Human_miRNA_ID_2872919,Human_miRNA_ID_2980883,Human_miRNA_ID_2980884 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103074 RMVar_ID_103074 Human_SNP_ID_302953847 m1A Human chr6 + 156778204 156778198 156778204 CCAGCAGCACCACCACCACCACCATGCCCACCACCACCACCACCATGCCCACCACCTCCACCACC CCAGCAGCACCACCACCACCACCATGC______CCACCACCACCATGCCCACCACCTCCACCACC CCCACCA C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156777818..156778491 26863196 MeRIP-seq:(Medium) rs754114025 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_26533258 Human_miRNA_ID_2492758,Human_miRNA_ID_2872918,Human_miRNA_ID_2872919,Human_miRNA_ID_2980883,Human_miRNA_ID_2980884 Clinvar_Rec_640 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103075 RMVar_ID_103075 Human_SNP_ID_302953848 m1A Human chr6 + 156778204 156778198 156778204 CCAGCAGCACCACCACCACCACCATGCCCACCACCACCACCACCATGCCCACCACCTCCACCACC CCAGCAGCACCACCACCACCACCATGCCCA___CCACCACCACCATGCCCACCACCTCCACCACC CCCACCA CCCA ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156777818..156778491 26863196 MeRIP-seq:(Medium) rs754114025 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_26533258 Human_miRNA_ID_2492758,Human_miRNA_ID_2872918,Human_miRNA_ID_2872919,Human_miRNA_ID_2980883,Human_miRNA_ID_2980884 Clinvar_Rec_640 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103076 RMVar_ID_103076 Human_SNP_ID_302954064 m1A Human chr6 - 156778427 156778427 156778427 GGCGGGCCCGGGGGGTCGGCCTGGCCGCCCGCAGCACTGTCCTTGGCGCCTCCATGTTGCGGCTG GGCGGGCCCGGGGGGTCGGCCTGGCCGCCCGCGGCACTGTCCTTGGCGCCTCCATGTTGCGGCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:156778379..156778498 26863196 MeRIP-seq:(Medium) rs1342382475 Functional Loss SNV dbSNP153 33..33 33 - - - 103077 RMVar_ID_103077 Human_SNP_ID_302954385 m1A Human chr6 - 156778945 156778934 156778946 CTGCTGCCGCCGCCGCCGCGGCCGCCGCCGCCACAGCTCCCGCTCCTGCTCCTCCTGCTCCTGCT CTGCTGCCGCCGCCGCCGCGGCCGCCGCCGC____________TCCTGCTCCTCCTGCTCCTGCT AGCGGGAGCTGTG A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:156778901..156779170 26863196 MeRIP-seq:(Medium) rs1203305031 Functional Loss DEL dbSNP153 32..43 33 - - - 103078 RMVar_ID_103078 Human_SNP_ID_302954410 m1A Human chr6 + 156778976 156778955 156778976 GTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGGGGG GTGGCGGCGGCG_____________________GCAGGAGGCGGCGGCGGCGGCGGCTATGGGGG GGCCGCGGCGGCGGCGGCAGCA G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:156778912..156778994 26863410 MeRIP-seq:(Medium) rs1205164383 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_251105,Human_RBP_ID_5532901 Human_miRNA_ID_2511415,Human_miRNA_ID_3054238 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103079 RMVar_ID_103079 Human_SNP_ID_302954413 m1A Human chr6 + 156778973 156778958 156778973 GCTGTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG GCTGTGGCGGCGGCGGCC_______________GCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG CGCGGCGGCGGCGGCA C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:156778708..156779471;chr6:156778725..156779449 26863196 MeRIP-seq:(Medium) rs1457993750 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_251105,Human_RBP_ID_5532901 Human_miRNA_ID_2511415,Human_miRNA_ID_3054238 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103080 RMVar_ID_103080 Human_SNP_ID_302954437 m1A Human chr6 + 156778973 156778973 156778973 GCTGTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG GCTGTGGCGGCGGCGGCCGCGGCGGCGGCGGCCGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG A C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:156778708..156779471;chr6:156778725..156779449 26863196 MeRIP-seq:(Medium) rs1331367859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251105,Human_RBP_ID_5532901 Human_miRNA_ID_2511415,Human_miRNA_ID_3054238 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103081 RMVar_ID_103081 Human_SNP_ID_302954441 m1A Human chr6 + 156778976 156778976 156778976 GTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGGGGG GTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCGGCAGGAGGCGGCGGCGGCGGCGGCTATGGGGG A G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:156778912..156778994 26863410 MeRIP-seq:(Medium) rs1339192099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251105,Human_RBP_ID_5532901 Human_miRNA_ID_2511415,Human_miRNA_ID_3054238 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103082 RMVar_ID_103082 Human_SNP_ID_302954558 m1A Human chr6 + 156779208 156779208 156779208 CCCCGACCCTCAATCAGCTGCTCACCTCGCCCAGCCCCATGATGCGGAGCTACGGCGGCAGCTAC CCCCGACCCTCAATCAGCTGCTCACCTCGCCCTGCCCCATGATGCGGAGCTACGGCGGCAGCTAC A T ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:156779124..156779327;chr6:156779028..156779250 26863196 MeRIP-seq:(Medium) rs1178936568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18857196 Human_miRNA_ID_2276451 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103083 RMVar_ID_103083 Human_SNP_ID_302959295 m1A Human chr6 + 156798002 156798002 156798002 CACTGAGGAATGCCCAGTAAGCCTGGGGGCTGACATTGTGGTCATTTCGTCACTGGTGACCTTCA CACTGAGGAATGCCCAGTAAGCCTGGGGGCTGGCATTGTGGTCATTTCGTCACTGGTGACCTTCA A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156797996..156798114 26863196 MeRIP-seq:(Medium) rs1395151193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 103084 RMVar_ID_103084 Human_SNP_ID_302967409 m1A Human chr6 + 156829400 156829400 156829400 ATCCAGGGTCGGACTCCCGGGGCCATGGCCGGAATGCAGTACCCTCAGCAGCAGGTTTGTGCTGG ATCCAGGGTCGGACTCCCGGGGCCATGGCCGGCATGCAGTACCCTCAGCAGCAGGTTTGTGCTGG A C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:156829188..156829456;chr6:156829173..156829473 26863196 MeRIP-seq:(Medium) rs1476110794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3798641,Human_RBP_ID_5152805,Human_RBP_ID_5532908,Human_RBP_ID_8905913,Human_RBP_ID_18195858,Human_RBP_ID_18449729,Human_RBP_ID_26355658 Human_Splice_Rec_826967,Human_Splice_Rec_827003,Human_Splice_Rec_827041,Human_Splice_Rec_827077,Human_Splice_Rec_827113,Human_Splice_Rec_827123,Human_Splice_Rec_827143,Human_Splice_Rec_827147,Human_Splice_Rec_827153,Human_Splice_Rec_827157,Human_Splice_Rec_827193,Human_Splice_Rec_827199,Human_Splice_Rec_827201 Human_miRNA_ID_2234490,Human_miRNA_ID_2234491,Human_miRNA_ID_3028645,Human_miRNA_ID_3028646 RMVar_hsa_circ_79458,RMVar_hsa_circ_242548,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_283730,RMVar_hsa_circ_352823,RMVar_hsa_circ_365634,RMVar_hsa_circ_242549,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_242561,RMVar_hsa_circ_75824,RMVar_hsa_circ_242560,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_242550,RMVar_hsa_circ_265538,RMVar_hsa_circ_242563,RMVar_hsa_circ_376546 103085 RMVar_ID_103085 Human_SNP_ID_302975351 m1A Human chr6 + 156862481 156862481 156862481 AAGAGGGCACAGTGAGAAAGTAAGACGAAGGCAGAACAGTAAGAGAAAAAAACCAGAAAAGAGCT AAGAGGGCACAGTGAGAAAGTAAGACGAAGGCTGAACAGTAAGAGAAAAAAACCAGAAAAGAGCT A T ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:156862479..156862671 26863196 MeRIP-seq:(Medium) rs1291289494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15702346 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_352823,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_242550 103086 RMVar_ID_103086 Human_SNP_ID_302985218 m1A Human chr6 + 156901471 156901471 156901471 TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCACCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCCCCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA A C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr6:156901422..156901557;chr6:156901345..156901554 26863196 MeRIP-seq:(Medium) rs756099753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251110,Human_RBP_ID_3970521,Human_RBP_ID_5532910,Human_RBP_ID_17422175,Human_RBP_ID_26355660 Human_Splice_Rec_826969,Human_Splice_Rec_827004,Human_Splice_Rec_827005,Human_Splice_Rec_827042,Human_Splice_Rec_827043,Human_Splice_Rec_827079,Human_Splice_Rec_827114,Human_Splice_Rec_827115,Human_Splice_Rec_827124,Human_Splice_Rec_827125,Human_Splice_Rec_827148,Human_Splice_Rec_827149,Human_Splice_Rec_827158,Human_Splice_Rec_827159,Human_Splice_Rec_827194,Human_Splice_Rec_827195,Human_Splice_Rec_827200,Human_Splice_Rec_827202,Human_Splice_Rec_827203,Human_Splice_Rec_827207 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_106096,RMVar_hsa_circ_242550,RMVar_hsa_circ_344061,RMVar_hsa_circ_276425,RMVar_hsa_circ_242565,RMVar_hsa_circ_242566,RMVar_hsa_circ_242567 103087 RMVar_ID_103087 Human_SNP_ID_302985219 m1A Human chr6 + 156901471 156901471 156901471 TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCACCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCGCCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA A G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr6:156901422..156901557;chr6:156901345..156901554 26863196 MeRIP-seq:(Medium) rs756099753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251110,Human_RBP_ID_3970521,Human_RBP_ID_5532910,Human_RBP_ID_17422175,Human_RBP_ID_26355660 Human_Splice_Rec_826969,Human_Splice_Rec_827004,Human_Splice_Rec_827005,Human_Splice_Rec_827042,Human_Splice_Rec_827043,Human_Splice_Rec_827079,Human_Splice_Rec_827114,Human_Splice_Rec_827115,Human_Splice_Rec_827124,Human_Splice_Rec_827125,Human_Splice_Rec_827148,Human_Splice_Rec_827149,Human_Splice_Rec_827158,Human_Splice_Rec_827159,Human_Splice_Rec_827194,Human_Splice_Rec_827195,Human_Splice_Rec_827200,Human_Splice_Rec_827202,Human_Splice_Rec_827203,Human_Splice_Rec_827207 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_106096,RMVar_hsa_circ_242550,RMVar_hsa_circ_344061,RMVar_hsa_circ_276425,RMVar_hsa_circ_242565,RMVar_hsa_circ_242566,RMVar_hsa_circ_242567 103088 RMVar_ID_103088 Human_SNP_ID_302988536 m1A Human chr6 - 156913721 156913721 156913721 TGGCATGGGCTGGGAGTTGGGAAGTGGATAGTAGGATGGTGGCTCACGGGCTGGGGCGGGCTGGT TGGCATGGGCTGGGAGTTGGGAAGTGGATAGTGGGATGGTGGCTCACGGGCTGGGGCGGGCTGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156913719..156913826 26863196 MeRIP-seq:(Medium) rs1226316032 Functional Loss SNV dbSNP153 33..33 33 - - - 103089 RMVar_ID_103089 Human_SNP_ID_303004370 m1A Human chr6 - 156976699 156976699 156976699 TTACAGCTTAAAAAGAGTCCACGGACCAGGAGAGTGAGCAGCAGCGCAGTTTACTGAACAAAGTG TTACAGCTTAAAAAGAGTCCACGGACCAGGAGGGTGAGCAGCAGCGCAGTTTACTGAACAAAGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:156976695..156976762 26863196 MeRIP-seq:(Medium) rs1047936396 Functional Loss SNV dbSNP153 33..33 33 - - - 103090 RMVar_ID_103090 Human_SNP_ID_303043072 m1A Human chr6 + 157131303 157131303 157131303 CCTCATGGAGCTAATGTTTTAGTGGGGAAGAGAGATGATAAGTGAGTCAAAATAAAATAAAGTGA CCTCATGGAGCTAATGTTTTAGTGGGGAAGAGGGATGATAAGTGAGTCAAAATAAAATAAAGTGA A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157131301..157131553 26863196 MeRIP-seq:(Medium) rs1177181230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_125692,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_4782,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_75824,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_108541,RMVar_hsa_circ_242550,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242571,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569,RMVar_hsa_circ_305696,RMVar_hsa_circ_279031,RMVar_hsa_circ_103831,RMVar_hsa_circ_124768,RMVar_hsa_circ_299017,RMVar_hsa_circ_242581,RMVar_hsa_circ_242582,RMVar_hsa_circ_317440,RMVar_hsa_circ_277083,RMVar_hsa_circ_242585,RMVar_hsa_circ_105739,RMVar_hsa_circ_124135,RMVar_hsa_circ_242587,RMVar_hsa_circ_242588,RMVar_hsa_circ_242586,RMVar_hsa_circ_242583,RMVar_hsa_circ_242584,RMVar_hsa_circ_276109,RMVar_hsa_circ_280937,RMVar_hsa_circ_293427,RMVar_hsa_circ_13273,RMVar_hsa_circ_42891,RMVar_hsa_circ_242595,RMVar_hsa_circ_242596,RMVar_hsa_circ_242594 103091 RMVar_ID_103091 Human_SNP_ID_303056476 m1A Human chr6 + 157184403 157184401 157184403 CCCGCCGGAAGTCTTCAGCACCGGGGACACCAAAAAGCAGCCCAAGCTCCAGCCGCCATCTCCTG CCCGCCGGAAGTCTTCAGCACCGGGGACACC__AAAGCAGCCCAAGCTCCAGCCGCCATCTCCTG CAA C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:157184352..157184470 26863196 MeRIP-seq:(Medium) rs886041493 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_19129849 Human_Splice_Rec_826987,Human_Splice_Rec_827025,Human_Splice_Rec_827061,Human_Splice_Rec_827097,Human_Splice_Rec_827177,Human_Splice_Rec_827227,Human_Splice_Rec_827261,Human_Splice_Rec_827305,Human_Splice_Rec_827335,Human_Splice_Rec_827361,Human_Splice_Rec_827391,Human_Splice_Rec_827415,Human_Splice_Rec_827443,Human_Splice_Rec_827463 RMVar_hsa_circ_79458,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_242551,RMVar_hsa_circ_242553,RMVar_hsa_circ_242552,RMVar_hsa_circ_242550,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569,RMVar_hsa_circ_105739,RMVar_hsa_circ_124135,RMVar_hsa_circ_242583,RMVar_hsa_circ_242584,RMVar_hsa_circ_13273,RMVar_hsa_circ_89886,RMVar_hsa_circ_242597,RMVar_hsa_circ_99139,RMVar_hsa_circ_242603,RMVar_hsa_circ_82954,RMVar_hsa_circ_242604,RMVar_hsa_circ_41829,RMVar_hsa_circ_76956,RMVar_hsa_circ_126727,RMVar_hsa_circ_321188,RMVar_hsa_circ_353685,RMVar_hsa_circ_242607,RMVar_hsa_circ_242608,RMVar_hsa_circ_73965,RMVar_hsa_circ_96244,RMVar_hsa_circ_62291,RMVar_hsa_circ_242609 103092 RMVar_ID_103092 Human_SNP_ID_303056478 m1A Human chr6 + 157184403 157184403 157184403 CCCGCCGGAAGTCTTCAGCACCGGGGACACCAAAAAGCAGCCCAAGCTCCAGCCGCCATCTCCTG CCCGCCGGAAGTCTTCAGCACCGGGGACACCATAAAGCAGCCCAAGCTCCAGCCGCCATCTCCTG A T ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:157184352..157184470 26863196 MeRIP-seq:(Medium) rs1348058133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19129849 Human_Splice_Rec_826987,Human_Splice_Rec_827025,Human_Splice_Rec_827061,Human_Splice_Rec_827097,Human_Splice_Rec_827177,Human_Splice_Rec_827227,Human_Splice_Rec_827261,Human_Splice_Rec_827305,Human_Splice_Rec_827335,Human_Splice_Rec_827361,Human_Splice_Rec_827391,Human_Splice_Rec_827415,Human_Splice_Rec_827443,Human_Splice_Rec_827463 RMVar_hsa_circ_79458,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_242551,RMVar_hsa_circ_242553,RMVar_hsa_circ_242552,RMVar_hsa_circ_242550,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569,RMVar_hsa_circ_105739,RMVar_hsa_circ_124135,RMVar_hsa_circ_242583,RMVar_hsa_circ_242584,RMVar_hsa_circ_13273,RMVar_hsa_circ_89886,RMVar_hsa_circ_242597,RMVar_hsa_circ_99139,RMVar_hsa_circ_242603,RMVar_hsa_circ_82954,RMVar_hsa_circ_242604,RMVar_hsa_circ_41829,RMVar_hsa_circ_76956,RMVar_hsa_circ_126727,RMVar_hsa_circ_321188,RMVar_hsa_circ_353685,RMVar_hsa_circ_242607,RMVar_hsa_circ_242608,RMVar_hsa_circ_73965,RMVar_hsa_circ_96244,RMVar_hsa_circ_62291,RMVar_hsa_circ_242609 103093 RMVar_ID_103093 Human_SNP_ID_303058156 m1A Human chr6 - 157190919 157190919 157190919 CCACCACCTCCTCATACACCAAGCTCATTCCCACCACCACCCCCATGACAGGTCCTCAGGGCCCT CCACCACCTCCTCATACACCAAGCTCATTCCCCCCACCACCCCCATGACAGGTCCTCAGGGCCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:157190917..157191013 26863196 MeRIP-seq:(Medium) rs1177061799 Functional Loss SNV dbSNP153 33..33 33 - - - 103094 RMVar_ID_103094 Human_SNP_ID_303061956 m1A Human chr6 - 157206352 157206352 157206352 TCATCCTCCTCGTCTTCCTCGTCGTCATCAATACATTCAGCATCTTCCTCCTCTTTCCCAGAATC TCATCCTCCTCGTCTTCCTCGTCGTCATCAATTCATTCAGCATCTTCCTCCTCTTTCCCAGAATC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:157206301..157206451 26863196 MeRIP-seq:(Medium) rs1554237142 Functional Loss SNV dbSNP153 33..33 33 - - - 103095 RMVar_ID_103095 Human_SNP_ID_303061958 m1A Human chr6 + 157206357 157206354 157206357 TGGGAAAGAGGAGGAAGATGCTGAATGTATTGATGACGACGAGGAAGACGAGGAGGATGAGGAGG TGGGAAAGAGGAGGAAGATGCTGAATGTAT___TGACGACGAGGAAGACGAGGAGGATGAGGAGG TTGA T ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157206306..157206466 26863196 MeRIP-seq:(Medium) rs771741082 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_78954,Human_RBP_ID_9309863,Human_RBP_ID_25979169,Human_RBP_ID_26355662,Human_RBP_ID_27090196 RMVar_hsa_circ_82954,RMVar_hsa_circ_242604 103096 RMVar_ID_103096 Human_SNP_ID_303088617 m1A Human chr6 - 157310582 157310578 157310582 GGCACACTGGGGCACTATGATGAGGCCGGGTGAGCGCACACTGGGGCACTATGATGAGGCTAGGT GGCACACTGGGGCACTATGATGAGGCCGGGTG____CACACTGGGGCACTATGATGAGGCTAGGT GCGCT G TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157310406..157310747 26863196 MeRIP-seq:(Medium) rs1562381965 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13249,Human_RBP_ID_9437587,Human_RBP_ID_18857353,Human_RBP_ID_23056591,Human_RBP_ID_24386941 103097 RMVar_ID_103097 Human_SNP_ID_303088715 m1A Human chr6 - 157310700 157310700 157310700 GATGAGGCTAGCTGAGTGCACACTGGGGCACTATGATGAGGCTAGGTGAGCGCACACTGGGACAC GATGAGGCTAGCTGAGTGCACACTGGGGCACTTTGATGAGGCTAGGTGAGCGCACACTGGGACAC T A TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157310445..157310750 26863196 MeRIP-seq:(Medium) rs1554248399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13250,Human_RBP_ID_10267774,Human_RBP_ID_15705815,Human_RBP_ID_23056593 103098 RMVar_ID_103098 Human_SNP_ID_303088716 m1A Human chr6 - 157310700 157310700 157310700 GATGAGGCTAGCTGAGTGCACACTGGGGCACTATGATGAGGCTAGGTGAGCGCACACTGGGACAC GATGAGGCTAGCTGAGTGCACACTGGGGCACTGTGATGAGGCTAGGTGAGCGCACACTGGGACAC T C TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157310445..157310750 26863196 MeRIP-seq:(Medium) rs1554248399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13250,Human_RBP_ID_10267774,Human_RBP_ID_15705815,Human_RBP_ID_23056593 103099 RMVar_ID_103099 Human_SNP_ID_303088717 m1A Human chr6 - 157310700 157310700 157310700 GATGAGGCTAGCTGAGTGCACACTGGGGCACTATGATGAGGCTAGGTGAGCGCACACTGGGACAC GATGAGGCTAGCTGAGTGCACACTGGGGCACTCTGATGAGGCTAGGTGAGCGCACACTGGGACAC T G TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157310445..157310750 26863196 MeRIP-seq:(Medium) rs1554248399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13250,Human_RBP_ID_10267774,Human_RBP_ID_15705815,Human_RBP_ID_23056593 103100 RMVar_ID_103100 Human_SNP_ID_303088820 m1A Human chr6 - 157310839 157310839 157310839 TATGATGAGGCTAGGTGAGTGCACACTGGGACACTATGATGAGGCCGGGTGAGTGCACACTGGGA TATGATGAGGCTAGGTGAGTGCACACTGGGACCCTATGATGAGGCCGGGTGAGTGCACACTGGGA T G TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157310814..157310880 26863196 MeRIP-seq:(Medium) rs9456378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10311873,Human_RBP_ID_15705821,Human_RBP_ID_23068375,Human_RBP_ID_25979194 103101 RMVar_ID_103101 Human_SNP_ID_303090296 m1A Human chr6 - 157312335 157312335 157312335 CACACTGGGACATGATGAGGCTAGGTGATTGCACACTGGGGCACTATAATGAGGTCAGATCAACG CACACTGGGACATGATGAGGCTAGGTGATTGCCCACTGGGGCACTATAATGAGGTCAGATCAACG T G TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157312301..157312666 26863196 MeRIP-seq:(Medium) rs1554249226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15705827 103102 RMVar_ID_103102 Human_SNP_ID_303091023 m1A Human chr6 - 157313014 157313014 157313014 TGCACACTGGGACACTATGATGAGGCTAGGTGAGCGGACACTGGGACACTATGATGAGGCTAGGT TGCACACTGGGACACTATGATGAGGCTAGGTGTGCGGACACTGGGACACTATGATGAGGCTAGGT T A TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:157312837..157313354;chr6:157312833..157313086 26863196 MeRIP-seq:(Medium) rs1554249566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13255,Human_RBP_ID_252727,Human_RBP_ID_791486,Human_RBP_ID_2986190,Human_RBP_ID_9437591,Human_RBP_ID_10267798,Human_RBP_ID_15705844,Human_RBP_ID_23056619 103103 RMVar_ID_103103 Human_SNP_ID_303091025 m1A Human chr6 + 157313016 157313016 157313016 CTAGCCTCATCATAGTGTCCCAGTGTCCGCTCACCTAGCCTCATCATAGTGTCCCAGTGTGCACT CTAGCCTCATCATAGTGTCCCAGTGTCCGCTCCCCTAGCCTCATCATAGTGTCCCAGTGTGCACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157312967..157313225 26863196 MeRIP-seq:(Medium) rs1554249568 Functional Loss SNV dbSNP153 33..33 33 - - - 103104 RMVar_ID_103104 Human_SNP_ID_303091027 m1A Human chr6 - 157313019 157313019 157313019 GTGAGTGCACACTGGGACACTATGATGAGGCTAGGTGAGCGGACACTGGGACACTATGATGAGGC GTGAGTGCACACTGGGACACTATGATGAGGCTCGGTGAGCGGACACTGGGACACTATGATGAGGC T G TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:157312969..157313072 26863196 MeRIP-seq:(Medium) rs1554249570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13255,Human_RBP_ID_252727,Human_RBP_ID_791486,Human_RBP_ID_2986190,Human_RBP_ID_9437591,Human_RBP_ID_10267798,Human_RBP_ID_15705844,Human_RBP_ID_23056619 103105 RMVar_ID_103105 Human_SNP_ID_303092108 m1A Human chr6 + 157314314 157314314 157314314 CATAGTGTCGCAGTGTGCACTCACCTGGCCTCATCATAGTGTCCCAGTGTGCACTCACCTGGCCT CATAGTGTCGCAGTGTGCACTCACCTGGCCTCCTCATAGTGTCCCAGTGTGCACTCACCTGGCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157314184..157314362 26863196 MeRIP-seq:(Medium) rs970634611 Functional Loss SNV dbSNP153 33..33 33 - - - 103106 RMVar_ID_103106 Human_SNP_ID_303092923 m1A Human chr6 - 157317537 157317537 157317537 CATTTAAAGCTGTGAGACTAGATTAACTCACCAAGGCAGTGAAGGTTGAAAGAAAAGAGAAGAGG CATTTAAAGCTGTGAGACTAGATTAACTCACCGAGGCAGTGAAGGTTGAAAGAAAAGAGAAGAGG T C TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:157317525..157317723 26863196 MeRIP-seq:(Medium) rs1554250458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15705977 103107 RMVar_ID_103107 Human_SNP_ID_303094152 m1A Human chr6 + 157322804 157322804 157322804 CCCGCTGCAGCAACGGTACCAAGGAAAATTCCACCTGCCAAGAGTTTCGGGGAGGAGGGGGGATA CCCGCTGCAGCAACGGTACCAAGGAAAATTCCCCCTGCCAAGAGTTTCGGGGAGGAGGGGGGATA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:157322764..157322842 26863196 MeRIP-seq:(Medium) rs782163291 Functional Loss SNV dbSNP153 33..33 33 - - - 103108 RMVar_ID_103108 Human_SNP_ID_303094153 m1A Human chr6 - 157322807 157322807 157322807 TAATATCCCCCCTCCTCCCCGAAACTCTTGGCAGGTGGAATTTTCCTTGGTACCGTTGCTGCAGC TAATATCCCCCCTCCTCCCCGAAACTCTTGGCTGGTGGAATTTTCCTTGGTACCGTTGCTGCAGC T A TMEM242 Ensembl:ENSG00000215712 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157322765..157322839 26863196 MeRIP-seq:(Medium) rs1554250825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4870567,Human_RBP_ID_9336339,Human_RBP_ID_9350711,Human_RBP_ID_26040849 103109 RMVar_ID_103109 Human_SNP_ID_303117329 m1A Human chr6 + 157420349 157420349 157420349 AAGGTATAGTCATTGAAGGGGTGGGCTGAGTCAAGGCACTGATGAGAGGAGAGAAGGTATAGGCA AAGGTATAGTCATTGAAGGGGTGGGCTGAGTCGAGGCACTGATGAGAGGAGAGAAGGTATAGGCA A G ZDHHC14 Ensembl:ENSG00000175048 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:157420213..157420501 26863196 MeRIP-seq:(Medium) rs530312806 Functional Loss SNV dbSNP153 33..33 33 - - - 103110 RMVar_ID_103110 Human_SNP_ID_303117332 m1A Human chr6 + 157420363 157420363 157420363 GAAGGGGTGGGCTGAGTCAAGGCACTGATGAGAGGAGAGAAGGTATAGGCATTGAAGGGGTGGGC GAAGGGGTGGGCTGAGTCAAGGCACTGATGAGGGGAGAGAAGGTATAGGCATTGAAGGGGTGGGC A G ZDHHC14 Ensembl:ENSG00000175048 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157420111..157420636 26863196 MeRIP-seq:(Medium) rs1355583145 Functional Loss SNV dbSNP153 33..33 33 - - - 103111 RMVar_ID_103111 Human_SNP_ID_303118819 m1A Human chr6 - 157426732 157426732 157426732 CCGTGGCCTGACTCCCTCCTAGTGCGGCTTCCAGCTCCCCATCCTTTCTGTTCCCTCCCACACAC CCGTGGCCTGACTCCCTCCTAGTGCGGCTTCCTGCTCCCCATCCTTTCTGTTCCCTCCCACACAC T A lnc-TMEM242-10,lnc-TMEM242-10:2 RNACentral:URS0000D5CDAF,RNACentral:URS0000D5A172 lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157426568..157426830 26863196 MeRIP-seq:(Medium) rs184871102 Functional Loss SNV dbSNP153 33..33 33 - - - 103112 RMVar_ID_103112 Human_SNP_ID_303118820 m1A Human chr6 - 157426732 157426732 157426732 CCGTGGCCTGACTCCCTCCTAGTGCGGCTTCCAGCTCCCCATCCTTTCTGTTCCCTCCCACACAC CCGTGGCCTGACTCCCTCCTAGTGCGGCTTCCGGCTCCCCATCCTTTCTGTTCCCTCCCACACAC T C lnc-TMEM242-10,lnc-TMEM242-10:2 RNACentral:URS0000D5CDAF,RNACentral:URS0000D5A172 lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157426568..157426830 26863196 MeRIP-seq:(Medium) rs184871102 Functional Loss SNV dbSNP153 33..33 33 - - - 103113 RMVar_ID_103113 Human_SNP_ID_303118836 m1A Human chr6 - 157426785 157426785 157426785 CGGCTTCCCGGCTTCTCTCCTGAGCTCTGTAGAACCTCACGCTGGCCCCTCTCCCGTGGCCTGAC CGGCTTCCCGGCTTCTCTCCTGAGCTCTGTAGGACCTCACGCTGGCCCCTCTCCCGTGGCCTGAC T C lnc-TMEM242-10,lnc-TMEM242-10:2 RNACentral:URS0000D5CDAF,RNACentral:URS0000D5A172 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:157426587..157426804 26863196 MeRIP-seq:(Medium) rs1205376140 Functional Loss SNV dbSNP153 33..33 33 - - - 103114 RMVar_ID_103114 Human_SNP_ID_303173073 m1A Human chr6 + 157650383 157650383 157650383 GTCAGGAGTGGGGGGCGAAGGGAGCTGGGCCGAGAACCAAGAGGTGAGACAAGACAAGGGGCGAG GTCAGGAGTGGGGGGCGAAGGGAGCTGGGCCGGGAACCAAGAGGTGAGACAAGACAAGGGGCGAG A G ZDHHC14 Ensembl:ENSG00000175048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157650177..157650429 26863196 MeRIP-seq:(Medium) rs1162868291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5327567 RMVar_hsa_circ_295793,RMVar_hsa_circ_278780,RMVar_hsa_circ_118931,RMVar_hsa_circ_49475,RMVar_hsa_circ_242612,RMVar_hsa_circ_242613,RMVar_hsa_circ_305415,RMVar_hsa_circ_105864,RMVar_hsa_circ_242615,RMVar_hsa_circ_242616,RMVar_hsa_circ_107660,RMVar_hsa_circ_242617 103115 RMVar_ID_103115 Human_SNP_ID_303173840 m1A Human chr6 + 157653288 157653288 157653288 AGTAGACAAGAGGGAGATGCTGTCATCTGAGCAGGCGACACGCCCTTGGCCTGGCGAGGAGGCAG AGTAGACAAGAGGGAGATGCTGTCATCTGAGCGGGCGACACGCCCTTGGCCTGGCGAGGAGGCAG A G ZDHHC14 Ensembl:ENSG00000175048 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:157653244..157653328 26863196 MeRIP-seq:(Medium) rs1000186020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13265 RMVar_hsa_circ_295793,RMVar_hsa_circ_278780,RMVar_hsa_circ_118931,RMVar_hsa_circ_49475,RMVar_hsa_circ_242612,RMVar_hsa_circ_242613,RMVar_hsa_circ_305415,RMVar_hsa_circ_105864,RMVar_hsa_circ_242615,RMVar_hsa_circ_242616,RMVar_hsa_circ_107660,RMVar_hsa_circ_242617 103116 RMVar_ID_103116 Human_SNP_ID_303214774 m1A Human chr6 - 157823270 157823270 157823270 CGCCTCGGCCCCGAGTCTCGACGCTCAGGCCCAGCCGCTGGGCGCTCGGCTACTCCCGCGCCGCA CGCCTCGGCCCCGAGTCTCGACGCTCAGGCCCGGCCGCTGGGCGCTCGGCTACTCCCGCGCCGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:157823097..157823396;chr6:157823091..157823481;chr6:157823222..157823380 26863196 MeRIP-seq:(Medium) rs938949179 Functional Loss SNV dbSNP153 33..33 33 - - - 103117 RMVar_ID_103117 Human_SNP_ID_303214775 m1A Human chr6 - 157823270 157823270 157823270 CGCCTCGGCCCCGAGTCTCGACGCTCAGGCCCAGCCGCTGGGCGCTCGGCTACTCCCGCGCCGCA CGCCTCGGCCCCGAGTCTCGACGCTCAGGCCCCGCCGCTGGGCGCTCGGCTACTCCCGCGCCGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:157823097..157823396;chr6:157823091..157823481;chr6:157823222..157823380 26863196 MeRIP-seq:(Medium) rs938949179 Functional Loss SNV dbSNP153 33..33 33 - - - 103118 RMVar_ID_103118 Human_SNP_ID_303232178 m1A Human chr6 - 157892054 157892054 157892054 ATCCTCTTTCTCTTCCCACTCCTTATTTTGCAAAGCTCTTAACTGTCCATCATGGGTAATTAAAA ATCCTCTTTCTCTTCCCACTCCTTATTTTGCAGAGCTCTTAACTGTCCATCATGGGTAATTAAAA T C AL035634.1 Ensembl:ENSG00000236324 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:157892045..157892257 26863196 MeRIP-seq:(Medium) rs999235173 Functional Loss SNV dbSNP153 33..33 33 - - - 103119 RMVar_ID_103119 Human_SNP_ID_303258258 m1A Human chr6 - 157997358 157997358 157997358 TTCTTATAAGCACGCCAGTCACATTGGATTAAAGGCCCACCCTATACCAGTACGATCCCATCTTA TTCTTATAAGCACGCCAGTCACATTGGATTAACGGCCCACCCTATACCAGTACGATCCCATCTTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:157997353..157997507 26863196 MeRIP-seq:(Medium) rs767354536 Functional Loss SNV dbSNP153 33..33 33 - - - 103120 RMVar_ID_103120 Human_SNP_ID_303263840 m1A Human chr6 + 158020223 158020223 158020223 GTGACTCTGACTGTGTGACCCCCACCTGCGTGACTCTGACTGTGTGACCCCCACCTGCGTGACTC GTGACTCTGACTGTGTGACCCCCACCTGCGTGCCTCTGACTGTGTGACCCCCACCTGCGTGACTC A C SYNJ2 Ensembl:ENSG00000078269 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158020219..158020324 26863196 MeRIP-seq:(Medium) rs1195124002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105070,RMVar_hsa_circ_295808,RMVar_hsa_circ_322803,RMVar_hsa_circ_319006,RMVar_hsa_circ_292560,RMVar_hsa_circ_242632,RMVar_hsa_circ_242633 103121 RMVar_ID_103121 Human_SNP_ID_303299245 m1A Human chr6 + 158158362 158158362 158158362 TGCAACAGATGACGCAATAAGCAGCCAGGGACATTCTGTGTAAGTAGAACAATTACAACAAATTT TGCAACAGATGACGCAATAAGCAGCCAGGGACCTTCTGTGTAAGTAGAACAATTACAACAAATTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158158333..158158431 26863196 MeRIP-seq:(Medium) rs140455198 Functional Loss SNV dbSNP153 33..33 33 - - - 103122 RMVar_ID_103122 Human_SNP_ID_303299247 m1A Human chr6 - 158158364 158158364 158158364 TTAAATTTGTTGTAATTGTTCTACTTACACAGAATGTCCCTGGCTGCTTATTGCGTCATCTGTTG TTAAATTTGTTGTAATTGTTCTACTTACACAGTATGTCCCTGGCTGCTTATTGCGTCATCTGTTG T A SERAC1 Ensembl:ENSG00000122335 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158158332..158158420 26863196 MeRIP-seq:(Medium) rs202043206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24143691 Human_Splice_Rec_827882,Human_Splice_Rec_827883,Human_Splice_Rec_827916,Human_Splice_Rec_827917,Human_Splice_Rec_827950,Human_Splice_Rec_827951,Human_Splice_Rec_827976,Human_Splice_Rec_827977,Human_Splice_Rec_828004,Human_Splice_Rec_828005,Human_Splice_Rec_828032,Human_Splice_Rec_828033,Human_Splice_Rec_828058,Human_Splice_Rec_828059,Human_Splice_Rec_828086,Human_Splice_Rec_828087,Human_Splice_Rec_828118,Human_Splice_Rec_828119,Human_Splice_Rec_828150,Human_Splice_Rec_828151,Human_Splice_Rec_828178,Human_Splice_Rec_828179,Human_Splice_Rec_828208,Human_Splice_Rec_828209,Human_Splice_Rec_828232,Human_Splice_Rec_828233,Human_Splice_Rec_828258,Human_Splice_Rec_828259,Human_Splice_Rec_828286,Human_Splice_Rec_828287,Human_Splice_Rec_828327 RMVar_hsa_circ_45467,RMVar_hsa_circ_242663,RMVar_hsa_circ_15858,RMVar_hsa_circ_307353,RMVar_hsa_circ_43777,RMVar_hsa_circ_242662,RMVar_hsa_circ_242661,RMVar_hsa_circ_346404,RMVar_hsa_circ_30074,RMVar_hsa_circ_337266 103123 RMVar_ID_103123 Human_SNP_ID_303319603 m1A Human chr6 - 158231911 158231911 158231911 GCCACCCCGGGAGACCCCCGCCCCCGGCCCGCACCGCGCCACGGTGCCCAAGATGCCCACAGTGC GCCACCCCGGGAGACCCCCGCCCCCGGCCCGCCCCGCGCCACGGTGCCCAAGATGCCCACAGTGC T G lnc-SERAC1-14 RNACentral:URS0000D5A2E8 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:158231882..158232029 26863196 MeRIP-seq:(Medium) rs1171920244 Functional Loss SNV dbSNP153 33..33 33 - - - 103124 RMVar_ID_103124 Human_SNP_ID_303319752 m1A Human chr6 + 158232220 158232220 158232220 GGGAGGCGGAGACTCGGCCGAGACGCGGGGGGAGGCGGCGGCGGCGGCGATGCGGGGCTGCTGGA GGGAGGCGGAGACTCGGCCGAGACGCGGGGGGGGGCGGCGGCGGCGGCGATGCGGGGCTGCTGGA A G lnc-TULP4-2 RNACentral:URS0000D5B539 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158232174..158232363 26863196 MeRIP-seq:(Medium) rs996605073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_828353 103125 RMVar_ID_103125 Human_SNP_ID_303353426 m1A Human chr6 + 158356769 158356769 158356769 GGACAAAAGGAGAGGGCAGTGCTGTAAGGTAGATGCCAAGGTGATGAAACAGAGGGGACCTGGAG GGACAAAAGGAGAGGGCAGTGCTGTAAGGTAGCTGCCAAGGTGATGAAACAGAGGGGACCTGGAG A C AL360169.2,TULP4 Ensembl:ENSG00000274023,Ensembl:ENSG00000130338 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158356750..158356891 26863196 MeRIP-seq:(Medium) rs1371647568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5619374 RMVar_hsa_circ_101982,RMVar_hsa_circ_242676 103126 RMVar_ID_103126 Human_SNP_ID_303369709 m1A Human chr6 + 158422585 158422585 158422585 GTGGAGCGGTTTTAAGGAGCGGAGAGTTTAATAGACAAGAAGGAAGCGGAAGGCAGAAGGAAGAG GTGGAGCGGTTTTAAGGAGCGGAGAGTTTAATGGACAAGAAGGAAGCGGAAGGCAGAAGGAAGAG A G AL360169.2,TULP4 Ensembl:ENSG00000274023,Ensembl:ENSG00000130338 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158422581..158422674 26863196 MeRIP-seq:(Medium) rs947817437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67216,RMVar_hsa_circ_101982,RMVar_hsa_circ_317035,RMVar_hsa_circ_242676,RMVar_hsa_circ_345961,RMVar_hsa_circ_271983,RMVar_hsa_circ_87397,RMVar_hsa_circ_242679,RMVar_hsa_circ_242680,RMVar_hsa_circ_242681,RMVar_hsa_circ_242678 103127 RMVar_ID_103127 Human_SNP_ID_303373281 m1A Human chr6 - 158435682 158435681 158435683 GTGACGGTGATGGTGTCGCAGTGTGAAGGACAAGAGCGATGAGCGCGGGATAGGTGTGGGGAGCC GTGACGGTGATGGTGTCGCAGTGTGAAGGAC__GAGCGATGAGCGCGGGATAGGTGTGGGGAGCC CTT C RF00017-4932 RNACentral:URS000096C9DE SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158435676..158435834 26863196 MeRIP-seq:(Medium) rs1266304396 Functional Loss DEL dbSNP153 32..33 33 - - - 103128 RMVar_ID_103128 Human_SNP_ID_303385923 m1A Human chr6 + 158484667 158484667 158484667 AGAAAGAGATCTCTCACCACGCACGTGCACCAAGGAGAGGACATATGAGGACACAGCGAAAAGAC AGAAAGAGATCTCTCACCACGCACGTGCACCAGGGAGAGGACATATGAGGACACAGCGAAAAGAC A G TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158484618..158484715 26863196 MeRIP-seq:(Medium) rs1047816361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15710552 RMVar_hsa_circ_87397,RMVar_hsa_circ_21989,RMVar_hsa_circ_104039,RMVar_hsa_circ_242681,RMVar_hsa_circ_364118,RMVar_hsa_circ_27346,RMVar_hsa_circ_293140,RMVar_hsa_circ_12683,RMVar_hsa_circ_101766,RMVar_hsa_circ_94481,RMVar_hsa_circ_242692,RMVar_hsa_circ_242693,RMVar_hsa_circ_242694,RMVar_hsa_circ_242691,RMVar_hsa_circ_87043,RMVar_hsa_circ_122696,RMVar_hsa_circ_242695,RMVar_hsa_circ_321873,RMVar_hsa_circ_28021,RMVar_hsa_circ_242696,RMVar_hsa_circ_242697,RMVar_hsa_circ_105107,RMVar_hsa_circ_242699,RMVar_hsa_circ_79528,RMVar_hsa_circ_242701 103129 RMVar_ID_103129 Human_SNP_ID_303391367 m1A Human chr6 - 158504002 158504002 158504002 CCGCCCGTCCTCCTTCTCACTGGCCCGCCGGCACTTGGCCTCCTCCAGCTCGCCGGCGGCCCGTG CCGCCCGTCCTCCTTCTCACTGGCCCGCCGGCCCTTGGCCTCCTCCAGCTCGCCGGCGGCCCGTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158503855..158504109 26863196 MeRIP-seq:(Medium) rs1481221879 Functional Loss SNV dbSNP153 33..33 33 - - - 103130 RMVar_ID_103130 Human_SNP_ID_303391398 m1A Human chr6 - 158504054 158504054 158504054 TCCACAGCGGCTGCTTGTTGGCCATCACGTACACGAAGCCTTGGCTGCCCAGCCGCCCGTCCTCC TCCACAGCGGCTGCTTGTTGGCCATCACGTACGCGAAGCCTTGGCTGCCCAGCCGCCCGTCCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158503869..158504101 26863196 MeRIP-seq:(Medium) rs1337658456 Functional Loss SNV dbSNP153 33..33 33 - - - 103131 RMVar_ID_103131 Human_SNP_ID_303406821 m1A Human chr6 + 158560520 158560520 158560520 GTTCCGGGACGGGGCTGCGAGCCACAGCGCTCACCGGGGGGCCGAGAGAACCGGGGGCGCTGCGG GTTCCGGGACGGGGCTGCGAGCCACAGCGCTCGCCGGGGGGCCGAGAGAACCGGGGGCGCTGCGG A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158560230..158560677 26863196 MeRIP-seq:(Medium) rs1253396968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3821907,Human_RBP_ID_5327249,Human_RBP_ID_8143664,Human_RBP_ID_9336801,Human_RBP_ID_18425762,Human_RBP_ID_18465647,Human_RBP_ID_18502780,Human_RBP_ID_22101661,Human_RBP_ID_22703115,Human_RBP_ID_22728240 RMVar_hsa_circ_76702,RMVar_hsa_circ_119909,RMVar_hsa_circ_83813,RMVar_hsa_circ_242708,RMVar_hsa_circ_242709,RMVar_hsa_circ_242710,RMVar_hsa_circ_242713,RMVar_hsa_circ_242714,RMVar_hsa_circ_242715,RMVar_hsa_circ_242712 103132 RMVar_ID_103132 Human_SNP_ID_303408680 m1A Human chr6 + 158566346 158566346 158566346 TCTCGCAAGCCCGAGACAGGATGAGATTACCAAGGGAGTGAGAGTAGAGAAGGGGAGGGGACAGA TCTCGCAAGCCCGAGACAGGATGAGATTACCAGGGGAGTGAGAGTAGAGAAGGGGAGGGGACAGA A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158566329..158566509 26863196 MeRIP-seq:(Medium) rs1234688104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7566698,Human_RBP_ID_10268572 RMVar_hsa_circ_76702,RMVar_hsa_circ_119909,RMVar_hsa_circ_83813,RMVar_hsa_circ_242708,RMVar_hsa_circ_242709,RMVar_hsa_circ_242710,RMVar_hsa_circ_242713,RMVar_hsa_circ_242714,RMVar_hsa_circ_242715,RMVar_hsa_circ_242712 103133 RMVar_ID_103133 Human_SNP_ID_303409175 m1A Human chr6 - 158568050 158568050 158568050 CCCCAGCACGCCAGTCCCACTGTTCAGGCCCCAAAAACTCCTGCCAGCTGCTGCCATCACCTCCA CCCCAGCACGCCAGTCCCACTGTTCAGGCCCCCAAAACTCCTGCCAGCTGCTGCCATCACCTCCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158567850..158568227 26863196 MeRIP-seq:(Medium) rs934587611 Functional Loss SNV dbSNP153 33..33 33 - - - 103134 RMVar_ID_103134 Human_SNP_ID_303430318 m1A Human chr6 - 158637850 158637850 158637850 GCAATTGGTGGTAACGCTTATCAACACAGCAAAGTGAACCAGTGGACCACAAATGTAGTAGAACA GCAATTGGTGGTAACGCTTATCAACACAGCAAGGTGAACCAGTGGACCACAAATGTAGTAGAACA T C DYNLT1 Ensembl:ENSG00000146425 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158637751..158641375 26863196 MeRIP-seq:(Medium) rs118095868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656289,Human_RBP_ID_947957,Human_RBP_ID_1666342,Human_RBP_ID_2012969,Human_RBP_ID_4905629,Human_RBP_ID_9401356,Human_RBP_ID_15712423,Human_RBP_ID_27829045 Human_Splice_Rec_828468,Human_Splice_Rec_828472,Human_Splice_Rec_828473,Human_Splice_Rec_828480 Human_miRNA_ID_2968200 RMVar_hsa_circ_26599,RMVar_hsa_circ_242763,RMVar_hsa_circ_242762,RMVar_hsa_circ_92200,RMVar_hsa_circ_242765,RMVar_hsa_circ_276300,RMVar_hsa_circ_281816,RMVar_hsa_circ_242764 103135 RMVar_ID_103135 Human_SNP_ID_303430333 m1A Human chr6 - 158637869 158637869 158637869 TTTCTAGGCTATAGAAAGCGCAATTGGTGGTAACGCTTATCAACACAGCAAAGTGAACCAGTGGA TTTCTAGGCTATAGAAAGCGCAATTGGTGGTAGCGCTTATCAACACAGCAAAGTGAACCAGTGGA T C DYNLT1 Ensembl:ENSG00000146425 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158637818..158637943 26863196 MeRIP-seq:(Medium) rs763411609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656290,Human_RBP_ID_947957,Human_RBP_ID_1666343,Human_RBP_ID_2012969,Human_RBP_ID_4905629,Human_RBP_ID_9401356,Human_RBP_ID_24144367,Human_RBP_ID_27342405,Human_RBP_ID_27829045 Human_Splice_Rec_828468,Human_Splice_Rec_828472,Human_Splice_Rec_828473,Human_Splice_Rec_828480 RMVar_hsa_circ_26599,RMVar_hsa_circ_242763,RMVar_hsa_circ_242762,RMVar_hsa_circ_92200,RMVar_hsa_circ_242765,RMVar_hsa_circ_276300,RMVar_hsa_circ_281816,RMVar_hsa_circ_242764 103136 RMVar_ID_103136 Human_SNP_ID_303430351 m1A Human chr6 - 158637896 158637896 158637896 TTAACCGGGACGCGCTTTGTGCTTTGTTTTCTAGGCTATAGAAAGCGCAATTGGTGGTAACGCTT TTAACCGGGACGCGCTTTGTGCTTTGTTTTCTGGGCTATAGAAAGCGCAATTGGTGGTAACGCTT T C DYNLT1 Ensembl:ENSG00000146425 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,Wild Type;HTR8/Svneo,Normoxia chr6:158637826..158637959;chr6:158637848..158637930 26863410,32194978 MeRIP-seq:(Medium) rs748124506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_947957,Human_RBP_ID_9401356,Human_RBP_ID_27829045 RMVar_hsa_circ_26599,RMVar_hsa_circ_242763,RMVar_hsa_circ_242762,RMVar_hsa_circ_92200,RMVar_hsa_circ_242765,RMVar_hsa_circ_276300 103137 RMVar_ID_103137 Human_SNP_ID_303431207 m1A Human chr6 - 158641320 158641318 158641320 TGTTGTTGATGAAGTGAGCAACATTGTAAAAGAGGTAAGAGGAGAAATGCTCACTTCTTAAATGT TGTTGTTGATGAAGTGAGCAACATTGTAAAAG__GTAAGAGGAGAAATGCTCACTTCTTAAATGT CCT C DYNLT1 Ensembl:ENSG00000146425 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:158641301..158641400 26863410 MeRIP-seq:(Medium) rs1375684945 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1666344,Human_RBP_ID_4904341,Human_RBP_ID_17663840,Human_RBP_ID_26354535 Human_Splice_Rec_828467,Human_Splice_Rec_828470,Human_Splice_Rec_828471,Human_Splice_Rec_828478,Human_Splice_Rec_828479 RMVar_hsa_circ_26599,RMVar_hsa_circ_242763,RMVar_hsa_circ_242762,RMVar_hsa_circ_92200,RMVar_hsa_circ_242765,RMVar_hsa_circ_276300 103138 RMVar_ID_103138 Human_SNP_ID_303431222 m1A Human chr6 - 158641362 158641361 158641363 TAAATCAAACTTAACTGAATGTTCTTCCTTACAGACTGCTTTTGTTGTTGATGAAGTGAGCAACA TAAATCAAACTTAACTGAATGTTCTTCCTTA__GACTGCTTTTGTTGTTGATGAAGTGAGCAACA CTG C DYNLT1 Ensembl:ENSG00000146425 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158641301..158641375 26863196 MeRIP-seq:(Medium) rs1156542957 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2987090,Human_RBP_ID_3799603 Human_Splice_Rec_828467,Human_Splice_Rec_828471,Human_Splice_Rec_828479 RMVar_hsa_circ_242763,RMVar_hsa_circ_92200 103139 RMVar_ID_103139 Human_SNP_ID_303431951 m1A Human chr6 - 158644301 158644301 158644301 GCCCCTTGCTCTGCGGGGCTGACCCCAGCCCCAGCCCCAGCCTGGAGCGGGGCGCGGCGGCCGGG GCCCCTTGCTCTGCGGGGCTGACCCCAGCCCCCGCCCCAGCCTGGAGCGGGGCGCGGCGGCCGGG T G DYNLT1 Ensembl:ENSG00000146425 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158644299..158644750 26863196 MeRIP-seq:(Medium) rs1470880091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22105492 RMVar_hsa_circ_242763,RMVar_hsa_circ_92200 103140 RMVar_ID_103140 Human_SNP_ID_303466093 m1A Human chr6 + 158766850 158766849 158766850 GGGAGTTCCTAGACTTGGAGCACTAAAGACACAAGCGTGGCGGGGCTGGCAGCGCCCGCTATGAG GGGAGTTCCTAGACTTGGAGCACTAAAGACAC_AGCGTGGCGGGGCTGGCAGCGCCCGCTATGAG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:158766726..158767100 32194978 MeRIP-seq:(Medium) rs1554270796 Functional Loss DEL dbSNP153 33..33 33 - - - 103141 RMVar_ID_103141 Human_SNP_ID_303466195 m1A Human chr6 - 158767038 158767037 158767039 CAGCGAGCTGTCCCAGGCCCGAGATGAGAATAAGAGGACCCACAATGACATCATCCACAACGAGA CAGCGAGCTGTCCCAGGCCCGAGATGAGAAT__GAGGACCCACAATGACATCATCCACAACGAGA CTT C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158766811..158767100 26863196 MeRIP-seq:(Medium) rs1212531370 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1666355,Human_RBP_ID_2012992,Human_RBP_ID_15712523,Human_RBP_ID_18538926,Human_RBP_ID_23056840 Human_Splice_Rec_828640,Human_Splice_Rec_828660,Human_Splice_Rec_828684 Human_miRNA_ID_2570408,Human_miRNA_ID_2570409,Human_miRNA_ID_2938367,Human_miRNA_ID_2938368,Human_miRNA_ID_3044160,Human_miRNA_ID_3044161 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_101157,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_104251,RMVar_hsa_circ_92418,RMVar_hsa_circ_98423,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_242780,RMVar_hsa_circ_83509,RMVar_hsa_circ_85329,RMVar_hsa_circ_242782,RMVar_hsa_circ_76147,RMVar_hsa_circ_242781,RMVar_hsa_circ_242778,RMVar_hsa_circ_242779,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_242771 103142 RMVar_ID_103142 Human_SNP_ID_303466326 m1A Human chr6 - 158767311 158767311 158767311 GTGAGGGCATCCGGGATGACCGCAATGAGGAGAAGCGCATCACTGAGGCAGAGAAGAACGAGCGT GTGAGGGCATCCGGGATGACCGCAATGAGGAGGAGCGCATCACTGAGGCAGAGAAGAACGAGCGT T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158766858..158767524 26863196 MeRIP-seq:(Medium) rs1562487890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79062,Human_RBP_ID_1394138,Human_RBP_ID_1666357,Human_RBP_ID_2987135,Human_RBP_ID_7567009,Human_RBP_ID_26355677,Human_RBP_ID_27568070 Human_Splice_Rec_828639,Human_Splice_Rec_828659,Human_Splice_Rec_828683 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_101157,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_104251,RMVar_hsa_circ_92418,RMVar_hsa_circ_98423,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_242780,RMVar_hsa_circ_83509,RMVar_hsa_circ_85329,RMVar_hsa_circ_242782,RMVar_hsa_circ_76147,RMVar_hsa_circ_242781,RMVar_hsa_circ_242778,RMVar_hsa_circ_242779,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_242771 103143 RMVar_ID_103143 Human_SNP_ID_303466437 m1A Human chr6 - 158767479 158767479 158767479 CCAAAGAAGCCCAGGATGACCTGGTGAAGACCAAGGAGGAGCTGCACCTGGTGATGACAGCACCC CCAAAGAAGCCCAGGATGACCTGGTGAAGACCGAGGAGGAGCTGCACCTGGTGATGACAGCACCC T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:158767251..158769950 32194978 MeRIP-seq:(Medium) rs757854700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79063,Human_RBP_ID_4908510,Human_RBP_ID_5217126,Human_RBP_ID_9336806,Human_RBP_ID_9401360,Human_RBP_ID_26354539 Human_Splice_Rec_828638,Human_Splice_Rec_828658,Human_Splice_Rec_828682 Human_miRNA_ID_2012198,Human_miRNA_ID_2012199,Human_miRNA_ID_2758566,Human_miRNA_ID_2758567 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_101157,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_104251,RMVar_hsa_circ_92418,RMVar_hsa_circ_98423,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_242780,RMVar_hsa_circ_83509,RMVar_hsa_circ_85329,RMVar_hsa_circ_242782,RMVar_hsa_circ_76147,RMVar_hsa_circ_242781,RMVar_hsa_circ_242778,RMVar_hsa_circ_242779,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_242771 103144 RMVar_ID_103144 Human_SNP_ID_303467675 m1A Human chr6 - 158770820 158770820 158770820 GAGAGAGAAAGAGCAGATGATGCGCGAGAAGGAGGAGTTGATGCTGCGGCTGCAGGACTATGAGG GAGAGAGAAAGAGCAGATGATGCGCGAGAAGGCGGAGTTGATGCTGCGGCTGCAGGACTATGAGG T G EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158769282..158771352 26863196 MeRIP-seq:(Medium) rs761523413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79070,Human_RBP_ID_3970549,Human_RBP_ID_7567020,Human_RBP_ID_9401364,Human_RBP_ID_19017641,Human_RBP_ID_22460830,Human_RBP_ID_26354544,Human_RBP_ID_27828131 Human_Splice_Rec_828632,Human_Splice_Rec_828633,Human_Splice_Rec_828652,Human_Splice_Rec_828653,Human_Splice_Rec_828676,Human_Splice_Rec_828677 Human_miRNA_ID_1936871,Human_miRNA_ID_1936872,Human_miRNA_ID_1947971,Human_miRNA_ID_1947972 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_92418,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_85329,RMVar_hsa_circ_76147,RMVar_hsa_circ_242778,RMVar_hsa_circ_242779,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_242783,RMVar_hsa_circ_34165,RMVar_hsa_circ_267771 103145 RMVar_ID_103145 Human_SNP_ID_303467683 m1A Human chr6 - 158770833 158770830 158770833 GAGAAACCGTGGAGAGAGAGAAAGAGCAGATGATGCGCGAGAAGGAGGAGTTGATGCTGCGGCTG GAGAAACCGTGGAGAGAGAGAAAGAGCAGATG___CGCGAGAAGGAGGAGTTGATGCTGCGGCTG GCAT G EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:158770688..158770953 26863196 MeRIP-seq:(Medium) rs768425876 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_79070,Human_RBP_ID_3970549,Human_RBP_ID_7567021,Human_RBP_ID_26354545,Human_RBP_ID_27829053 Human_Splice_Rec_828632,Human_Splice_Rec_828633,Human_Splice_Rec_828652,Human_Splice_Rec_828653,Human_Splice_Rec_828676,Human_Splice_Rec_828677 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_92418,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_85329,RMVar_hsa_circ_76147,RMVar_hsa_circ_242778,RMVar_hsa_circ_242779,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_242783,RMVar_hsa_circ_34165,RMVar_hsa_circ_267771 103146 RMVar_ID_103146 Human_SNP_ID_303467705 m1A Human chr6 - 158770896 158770896 158770896 TAAATCTCCCTGTGCCTCTTTTTCCCTGCACCAGGCAACAGCTGGAAACAGAGAAGAAAAGGAGA TAAATCTCCCTGTGCCTCTTTTTCCCTGCACCCGGCAACAGCTGGAAACAGAGAAGAAAAGGAGA T G EZR Ensembl:ENSG00000092820 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:158770751..158771425 32194978 MeRIP-seq:(Medium) rs112705375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79070,Human_RBP_ID_22683289 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_92418,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_76147,RMVar_hsa_circ_242778,RMVar_hsa_circ_242777,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_242783,RMVar_hsa_circ_34165,RMVar_hsa_circ_267771 103147 RMVar_ID_103147 Human_SNP_ID_303471861 m1A Human chr6 - 158785363 158785363 158785363 CTACGCTGTGCAGGCCAAGTTTGGGGACTACAACAAAGAAGTGCACAAGTCTGGGTACCTCAGCT CTACGCTGTGCAGGCCAAGTTTGGGGACTACAGCAAAGAAGTGCACAAGTCTGGGTACCTCAGCT T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158785277..158785442 26863196 MeRIP-seq:(Medium) rs929883961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2013005,Human_RBP_ID_3799633,Human_RBP_ID_9401367,Human_RBP_ID_17709830,Human_RBP_ID_22462273,Human_RBP_ID_22772940 Human_Splice_Rec_828623,Human_Splice_Rec_828643,Human_Splice_Rec_828667,Human_Splice_Rec_828693 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242773,RMVar_hsa_circ_54387,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786,RMVar_hsa_circ_298659,RMVar_hsa_circ_332275,RMVar_hsa_circ_65974,RMVar_hsa_circ_19359,RMVar_hsa_circ_110280,RMVar_hsa_circ_242788,RMVar_hsa_circ_46193,RMVar_hsa_circ_242789 103148 RMVar_ID_103148 Human_SNP_ID_303472978 m1A Human chr6 - 158789367 158789367 158789367 GCGTAATTTGTTTCATTCTGTTTTTCAGATCAATGTCCGAGTTACCACCATGGATGCAGAGCTGG GCGTAATTTGTTTCATTCTGTTTTTCAGATCAGTGTCCGAGTTACCACCATGGATGCAGAGCTGG T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158789276..158789375 26863196 MeRIP-seq:(Medium) rs144581330 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_79086,Human_RBP_ID_4908536,Human_RBP_ID_26828906 Human_Splice_Rec_828620,Human_Splice_Rec_828621,Human_Splice_Rec_828641,Human_Splice_Rec_828664,Human_Splice_Rec_828665,Human_Splice_Rec_828688,Human_Splice_Rec_828689 GWAS_ID_13427 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_125699,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_242786,RMVar_hsa_circ_298659,RMVar_hsa_circ_332275,RMVar_hsa_circ_19359,RMVar_hsa_circ_110280,RMVar_hsa_circ_242788,RMVar_hsa_circ_46193,RMVar_hsa_circ_242789 103149 RMVar_ID_103149 Human_SNP_ID_303481430 m1A Human chr6 - 158818168 158818168 158818168 GGCGGGCGCTCTAAGGGTTCTGCTCTGACTCCAGGTTGGGACAGCGTCTTCGCTGCTGCTGGATA GGCGGGCGCTCTAAGGGTTCTGCTCTGACTCCGGGTTGGGACAGCGTCTTCGCTGCTGCTGGATA T C EZR Ensembl:ENSG00000092820 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158818101..158818200 26863196 MeRIP-seq:(Medium) rs113471078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79098,Human_RBP_ID_4904342,Human_RBP_ID_19132301,Human_RBP_ID_22684521 Human_Splice_Rec_828619,Human_Splice_Rec_828663,Human_Splice_Rec_828687 Human_miRNA_ID_2723469,Human_miRNA_ID_2723470,Human_miRNA_ID_2723471 RMVar_hsa_circ_86438,RMVar_hsa_circ_242771,RMVar_hsa_circ_267771,RMVar_hsa_circ_97977,RMVar_hsa_circ_110280,RMVar_hsa_circ_242789,RMVar_hsa_circ_242790 103150 RMVar_ID_103150 Human_SNP_ID_303481652 m1A Human chr6 + 158818598 158818598 158818598 CCCGGGGAACACTCGGCCAGGAGGGTCAGGGGAGAGAGCGCCGGCCGGGCGGGGAGGGGTCTGGG CCCGGGGAACACTCGGCCAGGAGGGTCAGGGGTGAGAGCGCCGGCCGGGCGGGGAGGGGTCTGGG A T EZR-AS1 Ensembl:ENSG00000233893 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158818595..158818785 26863196 MeRIP-seq:(Medium) rs1203945808 Functional Loss SNV dbSNP153 33..33 33 - - - 103151 RMVar_ID_103151 Human_SNP_ID_303481886 m1A Human chr6 + 158819159 158819159 158819159 GAGGGGAAGGTCGCGGGGCCGCGGGCCGGCTCAGCTCCACCTGCCCCGGGGGTGCCGGGCGAGAA GAGGGGAAGGTCGCGGGGCCGCGGGCCGGCTCGGCTCCACCTGCCCCGGGGGTGCCGGGCGAGAA A G EZR-AS1 Ensembl:ENSG00000233893 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158819150..158819375 26863196 MeRIP-seq:(Medium) rs1397863164 Functional Loss SNV dbSNP153 33..33 33 - - - 103152 RMVar_ID_103152 Human_SNP_ID_303481905 m1A Human chr6 - 158819209 158819208 158819209 CGGGGTTCGGCGGCAGGTGCGGCGGGCAGCCTAGGGGGCGCGGCGCGGGGTTCTCGCCCGGCACC CGGGGTTCGGCGGCAGGTGCGGCGGGCAGCCT_GGGGGCGCGGCGCGGGGTTCTCGCCCGGCACC CT C EZR Ensembl:ENSG00000092820 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158819204..158819375 26863196 MeRIP-seq:(Medium) rs1394229421 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3820981,Human_RBP_ID_5134411,Human_RBP_ID_5327582,Human_RBP_ID_5400020,Human_RBP_ID_9336360,Human_RBP_ID_9437959,Human_RBP_ID_17091315,Human_RBP_ID_18465658,Human_RBP_ID_19129895,Human_RBP_ID_22728027,Human_RBP_ID_26792540 RMVar_hsa_circ_86438,RMVar_hsa_circ_242771 103153 RMVar_ID_103153 Human_SNP_ID_303481919 m1A Human chr6 + 158819236 158819236 158819236 CCCCCTAGGCTGCCCGCCGCACCTGCCGCCGAACCCCGCCGCCCGCCCGGGCCCTCCACCAGGAA CCCCCTAGGCTGCCCGCCGCACCTGCCGCCGAGCCCCGCCGCCCGCCCGGGCCCTCCACCAGGAA A G EZR-AS1 Ensembl:ENSG00000233893 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:158819227..158819375 26863196 MeRIP-seq:(Medium) rs961074513 Functional Loss SNV dbSNP153 33..33 33 - - - 103154 RMVar_ID_103154 Human_SNP_ID_303481920 m1A Human chr6 + 158819236 158819236 158819236 CCCCCTAGGCTGCCCGCCGCACCTGCCGCCGAACCCCGCCGCCCGCCCGGGCCCTCCACCAGGAA CCCCCTAGGCTGCCCGCCGCACCTGCCGCCGATCCCCGCCGCCCGCCCGGGCCCTCCACCAGGAA A T EZR-AS1 Ensembl:ENSG00000233893 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:158819227..158819375 26863196 MeRIP-seq:(Medium) rs961074513 Functional Loss SNV dbSNP153 33..33 33 - - - 103155 RMVar_ID_103155 Human_SNP_ID_303490504 m1A Human chr6 - 158853150 158853143 158853151 GTAAAGTATATGTGTGTGGCATATGGTGTGTGAGTGTGTATGTTGTACTGTGTGTGTGTGTATAT GTAAAGTATATGTGTGTGGCATATGGTGTGT________ATGTTGTACTGTGTGTGTGTGTATAT TACACACTC T OSTCP1 Ensembl:ENSG00000243775 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:158853006..158853172 26863196 MeRIP-seq:(Medium) rs1190498439 Functional Loss DEL dbSNP153 32..39 33 - - - 103156 RMVar_ID_103156 Human_SNP_ID_303526022 m1A Human chr6 + 158999523 158999518 158999524 GCTGGTGTAGGTGTAGGTGCTCGGGGCCCGAGAGGTGCGATCAGTCAGCGCTGAGGCCATGTCCG GCTGGTGTAGGTGTAGGTGCTCGGGGCC______GTGCGATCAGTCAGCGCTGAGGCCATGTCCG CCGAGAG C AL035530.2 Ensembl:ENSG00000271913 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158999473..158999765 26863196 MeRIP-seq:(Medium) rs1422484288 Functional Loss DEL dbSNP153 29..34 33 - - - 103157 RMVar_ID_103157 Human_SNP_ID_303526310 m1A Human chr6 - 159000010 159000010 159000010 AGCCCTGCAAAGCCACATTCCAAAGCCGGGCCAAGGACAGCCACCGTTGCCCCGCAGGCCTCAAG AGCCCTGCAAAGCCACATTCCAAAGCCGGGCCGAGGACAGCCACCGTTGCCCCGCAGGCCTCAAG T C RSPH3 Ensembl:ENSG00000130363 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158999960..159000133 26863196 MeRIP-seq:(Medium) rs779081089 Functional Loss SNV dbSNP153 33..33 33 - - - 103158 RMVar_ID_103158 Human_SNP_ID_303702908 m1A Human chr6 - 159693394 159693394 159693394 CGGGGTGTACGGCAAGCGCGGGCGGGCGGGACAGGCACGCAGGGCACCCCCGGGGTTGGGCGCGG CGGGGTGTACGGCAAGCGCGGGCGGGCGGGACCGGCACGCAGGGCACCCCCGGGGTTGGGCGCGG T G SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159693359..159693452 26863196 MeRIP-seq:(Medium) rs1356976654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4871508 103159 RMVar_ID_103159 Human_SNP_ID_303704485 m1A Human chr6 - 159699237 159699237 159699237 AGCAATGTCAAGCTTTAGGTCCAAGAGTGATGACCAGAGTCGTGTAAGAGATGGGACAGCAGGCC AGCAATGTCAAGCTTTAGGTCCAAGAGTGATGTCCAGAGTCGTGTAAGAGATGGGACAGCAGGCC T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159699080..159699281 26863196 MeRIP-seq:(Medium) rs1164079124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15714494 103160 RMVar_ID_103160 Human_SNP_ID_303707635 m1A Human chr6 - 159710798 159710798 159710798 AATGTGAGTGGTGGTTGTGGAGGCGGTTATGGAGGTCAGAGCAGCTGAGTGGTGGTTATGGAGGT AATGTGAGTGGTGGTTGTGGAGGCGGTTATGGTGGTCAGAGCAGCTGAGTGGTGGTTATGGAGGT T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:159710608..159710913;chr6:159710620..159710890 26863196 MeRIP-seq:(Medium) rs867031989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840262,Human_RBP_ID_17165193 103161 RMVar_ID_103161 Human_SNP_ID_303707669 m1A Human chr6 + 159710846 159710846 159710846 CAACCACCACTCACATTGCTCTGATCACCATAACCACCTCATAACCACCACTCAGCTGCTCTGAC CAACCACCACTCACATTGCTCTGATCACCATAGCCACCTCATAACCACCACTCAGCTGCTCTGAC A G lnc-WTAP-1,lnc-WTAP-1:2,lnc-WTAP-1:3 RNACentral:URS00008C10CE,RNACentral:URS00008C003D,RNACentral:URS00008C1567 lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159710604..159710898 26863196 MeRIP-seq:(Medium) rs543323025 Functional Loss SNV dbSNP153 33..33 33 - - - 103162 RMVar_ID_103162 Human_SNP_ID_303708092 m1A Human chr6 - 159711576 159711576 159711576 ATGGAGGTGGTTATGGTGGTCAGAGCAGTGTGAGTGGTGGTTGTGGAGGTGGTTATGGTGATCAG ATGGAGGTGGTTATGGTGGTCAGAGCAGTGTGGGTGGTGGTTGTGGAGGTGGTTATGGTGATCAG T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159711555..159711621 26863196 MeRIP-seq:(Medium) rs1386815556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840263,Human_RBP_ID_17165195,Human_RBP_ID_24144689 103163 RMVar_ID_103163 Human_SNP_ID_303708212 m1A Human chr6 + 159711703 159711702 159711703 GATCACCATAACCACCTCCATAACCACCACTCACACTGCTCTGATCACCATAACCACCTCCACAA GATCACCATAACCACCTCCATAACCACCACTC_CACTGCTCTGATCACCATAACCACCTCCACAA CA C lnc-WTAP-1,lnc-WTAP-1:2,lnc-WTAP-1:3 RNACentral:URS00008C10CE,RNACentral:URS00008C003D,RNACentral:URS00008C1567 lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159711684..159711753 26863196 MeRIP-seq:(Medium) rs1354244587 Functional Loss DEL dbSNP153 33..33 33 - - - 103164 RMVar_ID_103164 Human_SNP_ID_303708336 m1A Human chr6 - 159711882 159711852 159711882 TGATCAGAGCAATGTGAGTGGTGGTTATGGAGATCAGAGCAGTGTGACTGGTGGTTATGGAGGTG TGATCAGAGCAATGTGAGTGGTGGTTATGGAG______________________________GTG CCTCCATAACCACCAGTCACACTGCTCTGAT C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159711843..159711925 26863196 MeRIP-seq:(Medium) rs1246377204 Functional Loss DEL dbSNP153 33..62 33 - - - Human_RBP_ID_840327,Human_RBP_ID_24144691 103165 RMVar_ID_103165 Human_SNP_ID_303708349 m1A Human chr6 - 159711877 159711877 159711877 AGAGCAATGTGAGTGGTGGTTATGGAGATCAGAGCAGTGTGACTGGTGGTTATGGAGGTGGTTAT AGAGCAATGTGAGTGGTGGTTATGGAGATCAGCGCAGTGTGACTGGTGGTTATGGAGGTGGTTAT T G SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159711825..159711939 26863196 MeRIP-seq:(Medium) rs1485851305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840327,Human_RBP_ID_15714592,Human_RBP_ID_24144691 103166 RMVar_ID_103166 Human_SNP_ID_303708350 m1A Human chr6 - 159711879 159711879 159711879 TCAGAGCAATGTGAGTGGTGGTTATGGAGATCAGAGCAGTGTGACTGGTGGTTATGGAGGTGGTT TCAGAGCAATGTGAGTGGTGGTTATGGAGATCTGAGCAGTGTGACTGGTGGTTATGGAGGTGGTT T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159711825..159711910 26863196 MeRIP-seq:(Medium) rs1282884202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840327,Human_RBP_ID_24144691 103167 RMVar_ID_103167 Human_SNP_ID_303708352 m1A Human chr6 - 159711882 159711882 159711882 TGATCAGAGCAATGTGAGTGGTGGTTATGGAGATCAGAGCAGTGTGACTGGTGGTTATGGAGGTG TGATCAGAGCAATGTGAGTGGTGGTTATGGAGGTCAGAGCAGTGTGACTGGTGGTTATGGAGGTG T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159711843..159711925 26863196 MeRIP-seq:(Medium) rs62636459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840327,Human_RBP_ID_24144691 103168 RMVar_ID_103168 Human_SNP_ID_303708666 m1A Human chr6 - 159712237 159712235 159712238 GTGGTTATGGAGGTGGTTAGGGTGATCAGAGCAATGTGAGTGGTGGTTATGGAGGTGGTTATGGT GTGGTTATGGAGGTGGTTAGGGTGATCAGAG___TGTGAGTGGTGGTTATGGAGGTGGTTATGGT ATTG A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159712058..159712291 26863196 MeRIP-seq:(Medium) rs1250200612 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_840266,Human_RBP_ID_17165198,Human_RBP_ID_24144696 103169 RMVar_ID_103169 Human_SNP_ID_303708675 m1A Human chr6 + 159712247 159712244 159712248 CCTCCATAACCACCACTCACATTGCTCTGATCACCCTAACCACCTCCATAACCACCACTCACATT CCTCCATAACCACCACTCACATTGCTCTGA____CCTAACCACCTCCATAACCACCACTCACATT ATCAC A lnc-WTAP-1,lnc-WTAP-1:2 RNACentral:URS00008C10CE,RNACentral:URS00008C1567 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159712049..159712369 26863196 MeRIP-seq:(Medium) rs1562438383 Functional Loss DEL dbSNP153 31..34 33 - - - 103170 RMVar_ID_103170 Human_SNP_ID_303708679 m1A Human chr6 + 159712247 159712247 159712247 CCTCCATAACCACCACTCACATTGCTCTGATCACCCTAACCACCTCCATAACCACCACTCACATT CCTCCATAACCACCACTCACATTGCTCTGATCTCCCTAACCACCTCCATAACCACCACTCACATT A T lnc-WTAP-1,lnc-WTAP-1:2 RNACentral:URS00008C10CE,RNACentral:URS00008C1567 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159712049..159712369 26863196 MeRIP-seq:(Medium) rs1456534192 Functional Loss SNV dbSNP153 33..33 33 - - - 103171 RMVar_ID_103171 Human_SNP_ID_303708984 m1A Human chr6 - 159712626 159712597 159712626 GAGCATTGTGAGTGGTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGG GAGCATTGTGAGTGGTGGTTATGGAGGTGGTT_____________________________GTGG CAACGACCACTCAGCTGCTCTGACCTCCAT C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159712526..159712877 26863196 MeRIP-seq:(Medium) rs1562439059 Functional Loss DEL dbSNP153 33..61 33 - - - 103172 RMVar_ID_103172 Human_SNP_ID_303708994 m1A Human chr6 - 159712607 159712607 159712607 TATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGGGTGATCAG TATGGAGGTGGTTATGGAGGTCAGAGCAGCTGGGTGGTCGTTGTGGAGGCGGTTAGGGTGATCAG T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159712530..159712730 26863196 MeRIP-seq:(Medium) rs1438911758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840331,Human_RBP_ID_17165200 103173 RMVar_ID_103173 Human_SNP_ID_303708998 m1A Human chr6 - 159712612 159712611 159712612 GTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGGGTG GTGGTTATGGAGGTGGTTATGGAGGTCAGAGC_GCTGAGTGGTCGTTGTGGAGGCGGTTAGGGTG CT C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159712520..159712890 26863196 MeRIP-seq:(Medium) rs1326661496 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_840331,Human_RBP_ID_17165200 103174 RMVar_ID_103174 Human_SNP_ID_303708999 m1A Human chr6 - 159712612 159712612 159712612 GTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGGGTG GTGGTTATGGAGGTGGTTATGGAGGTCAGAGCTGCTGAGTGGTCGTTGTGGAGGCGGTTAGGGTG T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159712520..159712890 26863196 MeRIP-seq:(Medium) rs910057477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840331,Human_RBP_ID_17165200 103175 RMVar_ID_103175 Human_SNP_ID_303709002 m1A Human chr6 - 159712615 159712615 159712615 GTGGTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGG GTGGTGGTTATGGAGGTGGTTATGGAGGTCAGTGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGG T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:159712590..159712804 26863196 MeRIP-seq:(Medium) rs1465615147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840331,Human_RBP_ID_17165200 103176 RMVar_ID_103176 Human_SNP_ID_303709003 m1A Human chr6 - 159712615 159712615 159712615 GTGGTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGG GTGGTGGTTATGGAGGTGGTTATGGAGGTCAGGGCAGCTGAGTGGTCGTTGTGGAGGCGGTTAGG T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:159712590..159712804 26863196 MeRIP-seq:(Medium) rs1465615147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840331,Human_RBP_ID_17165200 103177 RMVar_ID_103177 Human_SNP_ID_303709014 m1A Human chr6 - 159712626 159712626 159712626 GAGCATTGTGAGTGGTGGTTATGGAGGTGGTTATGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGG GAGCATTGTGAGTGGTGGTTATGGAGGTGGTTGTGGAGGTCAGAGCAGCTGAGTGGTCGTTGTGG T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159712526..159712877 26863196 MeRIP-seq:(Medium) rs1056076020 Functional Loss SNV dbSNP153 33..33 33 - - - 103178 RMVar_ID_103178 Human_SNP_ID_303713137 m1A Human chr6 + 159727649 159727649 159727649 GTGGCCCGGGGGGCCCGGGCGGCAGGGCAAGCAGCGCGGCCTCGGCCTATGCGACCGGTGGCGCC GTGGCCCGGGGGGCCCGGGCGGCAGGGCAAGCGGCGCGGCCTCGGCCTATGCGACCGGTGGCGCC A G WTAP Ensembl:ENSG00000146457 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:159727328..159736348 26863410 MeRIP-seq:(Medium) rs1304686417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656493,Human_RBP_ID_841658,Human_RBP_ID_4903579,Human_RBP_ID_5327583,Human_RBP_ID_5401273,Human_RBP_ID_9401369,Human_RBP_ID_18171002,Human_RBP_ID_18425771,Human_RBP_ID_23067650,Human_RBP_ID_24144718 Human_Splice_Rec_829341,Human_Splice_Rec_829355,Human_Splice_Rec_829357,Human_Splice_Rec_829369 RMVar_hsa_circ_113323,RMVar_hsa_circ_78999,RMVar_hsa_circ_242804,RMVar_hsa_circ_95697,RMVar_hsa_circ_242805,RMVar_hsa_circ_242806 103179 RMVar_ID_103179 Human_SNP_ID_303716545 m1A Human chr6 - 159738978 159738978 159738978 GTCTGTTTCACTCAATCGAACCTATAAAGAGAATTACAATATGAATTTAGTGTTCTTCCTGAAGA GTCTGTTTCACTCAATCGAACCTATAAAGAGAGTTACAATATGAATTTAGTGTTCTTCCTGAAGA T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159738976..159739050 26863196 MeRIP-seq:(Medium) rs771382825 Functional Loss SNV dbSNP153 33..33 33 - - - 103180 RMVar_ID_103180 Human_SNP_ID_303720745 m1A Human chr6 + 159755432 159755432 159755432 GTTACGTAAATCAACTCAGTGCGGGGTATGAAAGTGTAGACTCTCCCACGGGCAGTGAAAACTCT GTTACGTAAATCAACTCAGTGCGGGGTATGAATGTGTAGACTCTCCCACGGGCAGTGAAAACTCT A T WTAP Ensembl:ENSG00000146457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159755382..159755495 26863196 MeRIP-seq:(Medium) rs1294982966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790490,Human_RBP_ID_1666495,Human_RBP_ID_2013192,Human_RBP_ID_7567993,Human_RBP_ID_9190556,Human_RBP_ID_15715699,Human_RBP_ID_18202754,Human_RBP_ID_18210894,Human_RBP_ID_18857818,Human_RBP_ID_24144802,Human_RBP_ID_26751315,Human_RBP_ID_27342516 RMVar_hsa_circ_113323,RMVar_hsa_circ_117156,RMVar_hsa_circ_242804,RMVar_hsa_circ_97970,RMVar_hsa_circ_242808,RMVar_hsa_circ_242810 103181 RMVar_ID_103181 Human_SNP_ID_303722944 m1A Human chr6 + 159762096 159762096 159762096 GCAGACGGCGGCAGGAGAAGCAAGATGAATGCAGGCTCAGATCCTGTGGTCATCGTCTCGGCGGC GCAGACGGCGGCAGGAGAAGCAAGATGAATGCGGGCTCAGATCCTGTGGTCATCGTCTCGGCGGC A G ACAT2 Ensembl:ENSG00000120437 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:159762026..159762175 26863196 MeRIP-seq:(Medium) rs1304919659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656562,Human_RBP_ID_4871646,Human_RBP_ID_8635811,Human_RBP_ID_9309448 Human_Splice_Rec_829383 103182 RMVar_ID_103182 Human_SNP_ID_303723159 m1A Human chr6 - 159762582 159762582 159762582 CGGGTCAAGGGCGTTGAAAACCATGCGGCACGAAGGAGACGAAGTCACGACTTCTAGCCATTGTG CGGGTCAAGGGCGTTGAAAACCATGCGGCACGTAGGAGACGAAGTCACGACTTCTAGCCATTGTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159762578..159762920 26863196 MeRIP-seq:(Medium) rs1562474093 Functional Loss SNV dbSNP153 33..33 33 - - - 103183 RMVar_ID_103183 Human_SNP_ID_303727488 m1A Human chr6 + 159778823 159778823 159778823 GGTGGGATGGGAATAGCAATGTGTGTTCAGAGAGAATGAATTGCTTAAACTTTGAACAACCTCAA GGTGGGATGGGAATAGCAATGTGTGTTCAGAGCGAATGAATTGCTTAAACTTTGAACAACCTCAA A C ACAT2 Ensembl:ENSG00000120437 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:159777313..159779055 32194978 MeRIP-seq:(Medium) rs1386916281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2013230,Human_RBP_ID_5151989,Human_RBP_ID_9309449,Human_RBP_ID_17663501,Human_RBP_ID_18544922,Human_RBP_ID_23214991,Human_RBP_ID_24144848,Human_RBP_ID_26355694 103184 RMVar_ID_103184 Human_SNP_ID_303730328 m1A Human chr6 - 159787776 159787776 159787776 GCTAAAGTTCTTTGTGAGCTGGCTGATCTGCAAGACAAAGAAGTTGGAGATGGAACTACTTCAGT GCTAAAGTTCTTTGTGAGCTGGCTGATCTGCAGGACAAAGAAGTTGGAGATGGAACTACTTCAGT T C TCP1 Ensembl:ENSG00000120438 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1285499502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13585,Human_RBP_ID_2013283,Human_RBP_ID_3799882,Human_RBP_ID_9402939,Human_RBP_ID_15716022,Human_RBP_ID_18085631,Human_RBP_ID_19129912 Human_Splice_Rec_829416,Human_Splice_Rec_829417,Human_Splice_Rec_829436,Human_Splice_Rec_829437,Human_Splice_Rec_829452,Human_Splice_Rec_829453,Human_Splice_Rec_829470,Human_Splice_Rec_829471,Human_Splice_Rec_829507,Human_Splice_Rec_829518,Human_Splice_Rec_829519,Human_Splice_Rec_829524,Human_Splice_Rec_829525,Human_Splice_Rec_829532,Human_Splice_Rec_829533,Human_Splice_Rec_829538,Human_Splice_Rec_829539,Human_Splice_Rec_829543,Human_Splice_Rec_829552,Human_Splice_Rec_829553,Human_Splice_Rec_829560,Human_Splice_Rec_829561 Human_miRNA_ID_1266120,Human_miRNA_ID_2611011,Human_miRNA_ID_2788739,Human_miRNA_ID_2818359 RMVar_hsa_circ_56423,RMVar_hsa_circ_242817,RMVar_hsa_circ_98318,RMVar_hsa_circ_356876,RMVar_hsa_circ_365525,RMVar_hsa_circ_367727,RMVar_hsa_circ_47508,RMVar_hsa_circ_295075,RMVar_hsa_circ_286986,RMVar_hsa_circ_97884,RMVar_hsa_circ_242827,RMVar_hsa_circ_242829,RMVar_hsa_circ_338628 103185 RMVar_ID_103185 Human_SNP_ID_303731001 m1A Human chr6 - 159789497 159789497 159789497 GGGCCGCGATACTGGTTGCCCGCGGTGTAAGCAGAATTCGACGTGTATCGCTGCCGTCAAGATGG GGGCCGCGATACTGGTTGCCCGCGGTGTAAGCGGAATTCGACGTGTATCGCTGCCGTCAAGATGG T C TCP1 Ensembl:ENSG00000120438 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:159789344..159789675 26863196 MeRIP-seq:(Medium) rs376808629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656618,Human_RBP_ID_1666553,Human_RBP_ID_2013291,Human_RBP_ID_3799889,Human_RBP_ID_4871794,Human_RBP_ID_8905918,Human_RBP_ID_9309872,Human_RBP_ID_9336813,Human_RBP_ID_18857872,Human_RBP_ID_24144899,Human_RBP_ID_24388719,Human_RBP_ID_27090778,Human_RBP_ID_27342578 Human_Splice_Rec_829413,Human_Splice_Rec_829435,Human_Splice_Rec_829449,Human_Splice_Rec_829469,Human_Splice_Rec_829491,Human_Splice_Rec_829503,Human_Splice_Rec_829515,Human_Splice_Rec_829523,Human_Splice_Rec_829529,Human_Splice_Rec_829547,Human_Splice_Rec_829563,Human_Splice_Rec_829565 103186 RMVar_ID_103186 Human_SNP_ID_303731042 m1A Human chr6 - 159789576 159789576 159789576 TTACCCAGTAGCTCCTGGGACATCGCTCGGGTACGCTCCACGCCGTCGCAGCCACTGCTGTGGTC TTACCCAGTAGCTCCTGGGACATCGCTCGGGTGCGCTCCACGCCGTCGCAGCCACTGCTGTGGTC T C TCP1 Ensembl:ENSG00000120438 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:159789332..159789675 26863196 MeRIP-seq:(Medium) rs950879592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81611,Human_RBP_ID_252131,Human_RBP_ID_656623,Human_RBP_ID_792078,Human_RBP_ID_1666556,Human_RBP_ID_4871795,Human_RBP_ID_5152817,Human_RBP_ID_5327255,Human_RBP_ID_7568186,Human_RBP_ID_8635868,Human_RBP_ID_8898127,Human_RBP_ID_9307930,Human_RBP_ID_9336365,Human_RBP_ID_22307445,Human_RBP_ID_22426617,Human_RBP_ID_22460839 103187 RMVar_ID_103187 Human_SNP_ID_303731047 m1A Human chr6 + 159789586 159789586 159789586 GTGGCTGCGACGGCGTGGAGCGTACCCGAGCGATGTCCCAGGAGCTACTGGGTAACACACCACCC GTGGCTGCGACGGCGTGGAGCGTACCCGAGCGCTGTCCCAGGAGCTACTGGGTAACACACCACCC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,Wild Type;HEK293T,H2O2 treatment chr6:159789489..159789616;chr6:159789499..159789600 26863410 MeRIP-seq:(Medium) rs1328025961 Functional Loss SNV dbSNP153 33..33 33 - - - 103188 RMVar_ID_103188 Human_SNP_ID_303731249 m1A Human chr6 - 159790012 159790012 159790012 GCAAAGCCGGCCGATCTGCCTCACGCTCCCCGAGCAGGGACAAGGAAAAGACACTAAACCTAAAA GCAAAGCCGGCCGATCTGCCTCACGCTCCCCGTGCAGGGACAAGGAAAAGACACTAAACCTAAAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159789961..159790075 26863196 MeRIP-seq:(Medium) rs1049391197 Functional Loss SNV dbSNP153 33..33 33 - - - 103189 RMVar_ID_103189 Human_SNP_ID_303731482 m1A Human chr6 - 159790525 159790525 159790525 CTTTTTCCTCACGGACGACTCAGTCGCTCGCCAGGAGCAGCCATATAAAGTCAGGGACAAGCCTT CTTTTTCCTCACGGACGACTCAGTCGCTCGCCGGGAGCAGCCATATAAAGTCAGGGACAAGCCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159790476..159790591 26863196 MeRIP-seq:(Medium) rs944430126 Functional Loss SNV dbSNP153 33..33 33 - - - 103190 RMVar_ID_103190 Human_SNP_ID_303731483 m1A Human chr6 - 159790525 159790525 159790525 CTTTTTCCTCACGGACGACTCAGTCGCTCGCCAGGAGCAGCCATATAAAGTCAGGGACAAGCCTT CTTTTTCCTCACGGACGACTCAGTCGCTCGCCCGGAGCAGCCATATAAAGTCAGGGACAAGCCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:159790476..159790591 26863196 MeRIP-seq:(Medium) rs944430126 Functional Loss SNV dbSNP153 33..33 33 - - - 103191 RMVar_ID_103191 Human_SNP_ID_303731536 m1A Human chr6 - 159790595 159790595 159790595 AAACCGAGAACAACCCCCAAAACCGCGACCGAAGCGCCATCGCTGAGACGATCTCGGAAAAGCCT AAACCGAGAACAACCCCCAAAACCGCGACCGAGGCGCCATCGCTGAGACGATCTCGGAAAAGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159790451..159790653 26863196 MeRIP-seq:(Medium) rs1289637573 Functional Loss SNV dbSNP153 33..33 33 - - - 103192 RMVar_ID_103192 Human_SNP_ID_303733546 m1A Human chr6 + 159797408 159797408 159797408 GGGCTATTAAAAAGCACCTTTATAGTACCAGAAATGTGGTGGCTTGTGAGAGTATAGGACGAGTG GGGCTATTAAAAAGCACCTTTATAGTACCAGATATGTGGTGGCTTGTGAGAGTATAGGACGAGTG A T MRPL18 Ensembl:ENSG00000112110 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159797358..159797442 26863196 MeRIP-seq:(Medium) rs1401107636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656627,Human_RBP_ID_2013300,Human_RBP_ID_4871846,Human_RBP_ID_7568229,Human_RBP_ID_8635873,Human_RBP_ID_9190580,Human_RBP_ID_15716231,Human_RBP_ID_17663844,Human_RBP_ID_24144910,Human_RBP_ID_27090788 Human_miRNA_ID_2779382 RMVar_hsa_circ_242830,RMVar_hsa_circ_76188,RMVar_hsa_circ_118656,RMVar_hsa_circ_242831 103193 RMVar_ID_103193 Human_SNP_ID_303733570 m1A Human chr6 + 159797467 159797467 159797467 CGAGTGCTGGCACAGAGATGCTTAGAGGCGGGAATCAACTTCATGGTCTACCAACCAACCCCGTG CGAGTGCTGGCACAGAGATGCTTAGAGGCGGGCATCAACTTCATGGTCTACCAACCAACCCCGTG A C MRPL18 Ensembl:ENSG00000112110 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159797266..159797545 26863196 MeRIP-seq:(Medium) rs761987625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1045410,Human_RBP_ID_15716232,Human_RBP_ID_17663504,Human_RBP_ID_18068834 Human_Splice_Rec_829571,Human_Splice_Rec_829583,Human_Splice_Rec_829589 Human_miRNA_ID_1167128,Human_miRNA_ID_2463941,Human_miRNA_ID_2560791 RMVar_hsa_circ_242830,RMVar_hsa_circ_76188,RMVar_hsa_circ_118656,RMVar_hsa_circ_242831 103194 RMVar_ID_103194 Human_SNP_ID_303733701 m1A Human chr6 - 159798032 159798032 159798032 GTAGTCGTTTCATCTGGTTTTGAAAATCAGAAAAAAAAGGAAAAGATTAAGTCAGCAGCACGAGT GTAGTCGTTTCATCTGGTTTTGAAAATCAGAAGAAAAAGGAAAAGATTAAGTCAGCAGCACGAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159798029..159798178 26863196 MeRIP-seq:(Medium) rs776664721 Functional Loss SNV dbSNP153 33..33 33 - - - 103195 RMVar_ID_103195 Human_SNP_ID_303783854 m1A Human chr6 + 159991220 159991220 159991220 ACATGGGAAGCTGTTGATACCAAAAATAATGTACTTTATAAAATCAACATCTGTGGAAGTGTGGA ACATGGGAAGCTGTTGATACCAAAAATAATGTGCTTTATAAAATCAACATCTGTGGAAGTGTGGA A G IGF2R Ensembl:ENSG00000197081 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:159991185..159991286 32194978 MeRIP-seq:(Medium) rs1447742035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2013309,Human_RBP_ID_3799914,Human_RBP_ID_17709851,Human_RBP_ID_21902624 Human_Splice_Rec_829754 Human_miRNA_ID_1754322,Human_miRNA_ID_2062818,Human_miRNA_ID_2448289,Human_miRNA_ID_2900488 RMVar_hsa_circ_121139,RMVar_hsa_circ_121692,RMVar_hsa_circ_77433,RMVar_hsa_circ_242836,RMVar_hsa_circ_119716,RMVar_hsa_circ_242837,RMVar_hsa_circ_333999,RMVar_hsa_circ_242835,RMVar_hsa_circ_355285,RMVar_hsa_circ_296817,RMVar_hsa_circ_242838,RMVar_hsa_circ_9030 103196 RMVar_ID_103196 Human_SNP_ID_303787034 m1A Human chr6 - 160004569 160004567 160004569 GCCAGGCCACACCACCCAGCACTCCAAGCTACACTCACTAGACCCACCCGGAAAAACAGGCCACA GCCAGGCCACACCACCCAGCACTCCAAGCTAC__TCACTAGACCCACCCGGAAAAACAGGCCACA AGT A AIRN Ensembl:ENSG00000268257 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:160004563..160004682 26863196 MeRIP-seq:(Medium) rs1197843521 Functional Loss DEL dbSNP153 33..34 33 - - - 103197 RMVar_ID_103197 Human_SNP_ID_303794409 m1A Human chr6 + 160032666 160032666 160032666 CCTGGAAAGTAAAACTTGTTCTCTGAGCGGCGAGCAGCAGGATGTCTCCATAGACCTCACACCAC CCTGGAAAGTAAAACTTGTTCTCTGAGCGGCGGGCAGCAGGATGTCTCCATAGACCTCACACCAC A G IGF2R Ensembl:ENSG00000197081 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:160032617..160033095 32194978 MeRIP-seq:(Medium) rs200914162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970557,Human_RBP_ID_5532954,Human_RBP_ID_22461494,Human_RBP_ID_22772947 Human_Splice_Rec_829767,Human_Splice_Rec_829845 Human_miRNA_ID_2511425,Human_miRNA_ID_3054248 RMVar_hsa_circ_1379,RMVar_hsa_circ_121139,RMVar_hsa_circ_121692,RMVar_hsa_circ_77433,RMVar_hsa_circ_242836,RMVar_hsa_circ_119716,RMVar_hsa_circ_242837,RMVar_hsa_circ_242835,RMVar_hsa_circ_94363,RMVar_hsa_circ_242838,RMVar_hsa_circ_9030,RMVar_hsa_circ_111491,RMVar_hsa_circ_242839,RMVar_hsa_circ_242840,RMVar_hsa_circ_101920,RMVar_hsa_circ_6013,RMVar_hsa_circ_27819,RMVar_hsa_circ_75765,RMVar_hsa_circ_316197,RMVar_hsa_circ_242841,RMVar_hsa_circ_92773,RMVar_hsa_circ_242842,RMVar_hsa_circ_242843,RMVar_hsa_circ_103189,RMVar_hsa_circ_58038,RMVar_hsa_circ_119924,RMVar_hsa_circ_242844,RMVar_hsa_circ_317280,RMVar_hsa_circ_111896,RMVar_hsa_circ_13314,RMVar_hsa_circ_242845,RMVar_hsa_circ_242846 103198 RMVar_ID_103198 Human_SNP_ID_303805953 m1A Human chr6 + 160073387 160073387 160073387 TTTCGTGTGCAGGCCTGAGGCCAGGCCAACCAATAGGCCCATGCTCATCTCCCTGGACAAGCAGA TTTCGTGTGCAGGCCTGAGGCCAGGCCAACCACTAGGCCCATGCTCATCTCCCTGGACAAGCAGA A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs766092725 Functional Loss SNV dbSNP153 33..33 33 - - - 103199 RMVar_ID_103199 Human_SNP_ID_303805954 m1A Human chr6 + 160073387 160073387 160073387 TTTCGTGTGCAGGCCTGAGGCCAGGCCAACCAATAGGCCCATGCTCATCTCCCTGGACAAGCAGA TTTCGTGTGCAGGCCTGAGGCCAGGCCAACCAGTAGGCCCATGCTCATCTCCCTGGACAAGCAGA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs766092725 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 103200 RMVar_ID_103200 Human_SNP_ID_303813452 m1A Human chr6 - 160100824 160100821 160100825 ATCGCACCACTGCACTCCAGCCTGGGCAAAAGAGCAAGTCTCTGTCTCCAAAAAAAAAAAAAAAA ATCGCACCACTGCACTCCAGCCTGGGCAAAA____AAGTCTCTGTCTCCAAAAAAAAAAAAAAAA TGCTC T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:160100733..160100825 26863410 MeRIP-seq:(Medium) rs1173148988 Functional Loss DEL dbSNP153 32..35 33 - - - 103201 RMVar_ID_103201 Human_SNP_ID_303814662 m1A Human chr6 - 160104875 160104875 160104875 GTGGGAGCTCTCTGCCCCAGCTCCCCTGCCCGAGTGAACTTTCACCTCTGGGATGGTCAGAACCT GTGGGAGCTCTCTGCCCCAGCTCCCCTGCCCGGGTGAACTTTCACCTCTGGGATGGTCAGAACCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:160103759..160105073 26863196 MeRIP-seq:(Medium) rs939596714 Functional Loss SNV dbSNP153 33..33 33 - - - 103202 RMVar_ID_103202 Human_SNP_ID_303814917 m1A Human chr6 - 160105615 160105612 160105615 CCAACTCAGGGGACACATTAATGACCAGTTCAACATCCCGCCGGAAGCTGCCCCATACACTGACA CCAACTCAGGGGACACATTAATGACCAGTTCA___TCCCGCCGGAAGCTGCCCCATACACTGACA ATGT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:160105564..160105715 32194978 MeRIP-seq:(Medium) rs1382499815 Functional Loss DEL dbSNP153 33..35 33 - - - 103203 RMVar_ID_103203 Human_SNP_ID_303814920 m1A Human chr6 - 160105615 160105615 160105615 CCAACTCAGGGGACACATTAATGACCAGTTCAACATCCCGCCGGAAGCTGCCCCATACACTGACA CCAACTCAGGGGACACATTAATGACCAGTTCAGCATCCCGCCGGAAGCTGCCCCATACACTGACA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:160105564..160105715 32194978 MeRIP-seq:(Medium) rs905056419 Functional Loss SNV dbSNP153 33..33 33 - - - 103204 RMVar_ID_103204 Human_SNP_ID_303814944 m1A Human chr6 + 160105696 160105692 160105696 TTTCTCTTTTGCTTTCTGTTTCTTAAGGGCACACACACGTGCGTGCGAGCACACACACACATACG TTTCTCTTTTGCTTTCTGTTTCTTAAGGG____CACACGTGCGTGCGAGCACACACACACATACG GCACA G IGF2R Ensembl:ENSG00000197081 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:160105564..160105715 32194978 MeRIP-seq:(Medium) rs8191960 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_81111,Human_RBP_ID_790656,Human_RBP_ID_2987762,Human_RBP_ID_3799986,Human_RBP_ID_5122585,Human_RBP_ID_5151991,Human_RBP_ID_15718003,Human_RBP_ID_17309792,Human_RBP_ID_17538167,Human_RBP_ID_24145241,Human_RBP_ID_24435166,Human_RBP_ID_26540353 Human_miRNA_ID_324491 RMVar_hsa_circ_92773,RMVar_hsa_circ_242843,RMVar_hsa_circ_77441,RMVar_hsa_circ_242869 103205 RMVar_ID_103205 Human_SNP_ID_303814945 m1A Human chr6 + 160105696 160105692 160105696 TTTCTCTTTTGCTTTCTGTTTCTTAAGGGCACACACACGTGCGTGCGAGCACACACACACATACG TTTCTCTTTTGCTTTCTGTTTCTTAAGGGCA__CACACGTGCGTGCGAGCACACACACACATACG GCACA GCA IGF2R Ensembl:ENSG00000197081 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:160105564..160105715 32194978 MeRIP-seq:(Medium) rs8191960 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_81111,Human_RBP_ID_790656,Human_RBP_ID_2987762,Human_RBP_ID_3799986,Human_RBP_ID_5122585,Human_RBP_ID_5151991,Human_RBP_ID_15718003,Human_RBP_ID_17309792,Human_RBP_ID_17538167,Human_RBP_ID_24145241,Human_RBP_ID_24435166,Human_RBP_ID_26540353 Human_miRNA_ID_324491 RMVar_hsa_circ_92773,RMVar_hsa_circ_242843,RMVar_hsa_circ_77441,RMVar_hsa_circ_242869 103206 RMVar_ID_103206 Human_SNP_ID_303814947 m1A Human chr6 + 160105696 160105696 160105696 TTTCTCTTTTGCTTTCTGTTTCTTAAGGGCACACACACGTGCGTGCGAGCACACACACACATACG TTTCTCTTTTGCTTTCTGTTTCTTAAGGGCACGCACACGTGCGTGCGAGCACACACACACATACG A G IGF2R Ensembl:ENSG00000197081 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:160105564..160105715 32194978 MeRIP-seq:(Medium) rs756135632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81111,Human_RBP_ID_790656,Human_RBP_ID_2987762,Human_RBP_ID_3799986,Human_RBP_ID_5122585,Human_RBP_ID_5151991,Human_RBP_ID_15718003,Human_RBP_ID_17309792,Human_RBP_ID_17538167,Human_RBP_ID_24145241,Human_RBP_ID_24435166,Human_RBP_ID_26540353 Human_miRNA_ID_324491 RMVar_hsa_circ_92773,RMVar_hsa_circ_242843,RMVar_hsa_circ_77441,RMVar_hsa_circ_242869 103207 RMVar_ID_103207 Human_SNP_ID_303815109 m1A Human chr6 + 160106158 160106158 160106158 ATCATGGGCCAGAGCCTCGGCCCTAGCATTGCACTTGGCCTCATGCTGGAGGGAGGCTGGGCGGG ATCATGGGCCAGAGCCTCGGCCCTAGCATTGCGCTTGGCCTCATGCTGGAGGGAGGCTGGGCGGG A G IGF2R Ensembl:ENSG00000197081 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:160106108..160106275 26863196 MeRIP-seq:(Medium) rs1302971158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251756,Human_RBP_ID_5122588,Human_RBP_ID_5152478,Human_RBP_ID_8216275,Human_RBP_ID_17310094,Human_RBP_ID_17538168,Human_RBP_ID_26540356 Human_miRNA_ID_214491,Human_miRNA_ID_224029,Human_miRNA_ID_518349,Human_miRNA_ID_522582,Human_miRNA_ID_762541,Human_miRNA_ID_767442,Human_miRNA_ID_772345,Human_miRNA_ID_777182,Human_miRNA_ID_782048,Human_miRNA_ID_786895,Human_miRNA_ID_791707,Human_miRNA_ID_1108191,Human_miRNA_ID_1113032,Human_miRNA_ID_1327022,Human_miRNA_ID_1569024,Human_miRNA_ID_1574725,Human_miRNA_ID_1581884,Human_miRNA_ID_1601404,Human_miRNA_ID_1610860,Human_miRNA_ID_1615782,Human_miRNA_ID_1623266,Human_miRNA_ID_1639367,Human_miRNA_ID_2019132,Human_miRNA_ID_2024225,Human_miRNA_ID_2310845,Human_miRNA_ID_2312865,Human_miRNA_ID_2440996,Human_miRNA_ID_2498958,Human_miRNA_ID_2606741,Human_miRNA_ID_2654646,Human_miRNA_ID_2805501,Human_miRNA_ID_2808644,Human_miRNA_ID_2811787 RMVar_hsa_circ_92773,RMVar_hsa_circ_242843,RMVar_hsa_circ_77441,RMVar_hsa_circ_242869 103208 RMVar_ID_103208 Human_SNP_ID_303876190 m1A Human chr6 - 160348394 160348394 160348394 AGGGCATGGTGCGCCCGCCGCCCGCCGCCCGCAGCCCGCGCCTCGGAGTGACCCGCGGACCCAGC AGGGCATGGTGCGCCCGCCGCCCGCCGCCCGCCGCCCGCGCCTCGGAGTGACCCGCGGACCCAGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:160348097..160348518 26863196 MeRIP-seq:(Medium) rs948305669 Functional Loss SNV dbSNP153 33..33 33 - - - 103209 RMVar_ID_103209 Human_SNP_ID_303876376 m1A Human chr6 + 160348718 160348685 160348718 CTGCCAGCGCTACCTCCTGGAGGCGGCCAACGACAGCGCCTCCGCCACTAGCGCTCTCAGCTGCG _________________________________CAGCGCCTCCGCCACTAGCGCTCTCAGCTGCG GCTGCCAGCGCTACCTCCTGGAGGCGGCCAACGA G SLC22A3 Ensembl:ENSG00000146477 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:160348668..160348765 26863196 MeRIP-seq:(Medium) rs1194798712 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_242871,RMVar_hsa_circ_102909 103210 RMVar_ID_103210 Human_SNP_ID_303898624 m1A Human chr6 + 160446464 160446464 160446464 GGAAGCCTCAGGAAACTTACAATCATGGTGGAAGGGGAAGCAGGCACGTCCTACATGGTGGCAGG GGAAGCCTCAGGAAACTTACAATCATGGTGGACGGGGAAGCAGGCACGTCCTACATGGTGGCAGG A C SLC22A3 Ensembl:ENSG00000146477 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:160446416..160446559;chr6:160446398..160446495 26863196 MeRIP-seq:(Medium) rs1395369357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376217,RMVar_hsa_circ_242878,RMVar_hsa_circ_372897,RMVar_hsa_circ_55829,RMVar_hsa_circ_242879 103211 RMVar_ID_103211 Human_SNP_ID_303898781 m1A Human chr6 - 160447129 160447129 160447129 CCAGCCTTCTCTCAATCTCACCTCATCCTTCCATTACCATCCTTTCTTTTTCTGCTCTTTAGAGC CCAGCCTTCTCTCAATCTCACCTCATCCTTCCGTTACCATCCTTTCTTTTTCTGCTCTTTAGAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:160447078..160447220 26863196 MeRIP-seq:(Medium) rs1447287818 Functional Loss SNV dbSNP153 33..33 33 - - - 103212 RMVar_ID_103212 Human_SNP_ID_304036792 m1A Human chr6 + 160992027 160992027 160992027 ATGGAGGAGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAACCCGAGACCGAGTCAGA ATGGAGGAGCCGCCGCCACCGCCGCCGCCGCCGCCACCGCCACCGGAACCCGAGACCGAGTCAGA A G MAP3K4 Ensembl:ENSG00000085511 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:160991859..160992033 26863196 MeRIP-seq:(Medium) rs1562464630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_830447,Human_Splice_Rec_830497,Human_Splice_Rec_830501,Human_Splice_Rec_830553,Human_Splice_Rec_830605,Human_Splice_Rec_830655,Human_Splice_Rec_830709 103213 RMVar_ID_103213 Human_SNP_ID_304056089 m1A Human chr6 - 161069479 161069477 161069480 CACCCTCCAGTGCTGCCTTCTCTCCTGCCTCCACGTGACACTCTCAACCAACCCTCACACACGTG CACCCTCCAGTGCTGCCTTCTCTCCTGCCTC___GTGACACTCTCAACCAACCCTCACACACGTG CGTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:161069331..161069630 26863196 MeRIP-seq:(Medium) rs1407267398 Functional Loss DEL dbSNP153 32..34 33 - - - 103214 RMVar_ID_103214 Human_SNP_ID_304056094 m1A Human chr6 + 161069494 161069494 161069494 TGGTTGAGAGTGTCACGTGGAGGCAGGAGAGAAGGCAGCACTGGAGGGTGAGACTAGGTCATGGA TGGTTGAGAGTGTCACGTGGAGGCAGGAGAGACGGCAGCACTGGAGGGTGAGACTAGGTCATGGA A C MAP3K4 Ensembl:ENSG00000085511 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:161069333..161069629 26863196 MeRIP-seq:(Medium) rs1158584910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7569175,Human_RBP_ID_15719550,Human_RBP_ID_23294992 RMVar_hsa_circ_14904,RMVar_hsa_circ_113190,RMVar_hsa_circ_70888,RMVar_hsa_circ_242891,RMVar_hsa_circ_266324 103215 RMVar_ID_103215 Human_SNP_ID_304056208 m1A Human chr6 + 161069874 161069874 161069874 GACCAAAGGGAGGAGAAGCAGGGGCCTTGGGGAGCCAGGGAGGAGTGACCAGGAGCAGAGAGAGT GACCAAAGGGAGGAGAAGCAGGGGCCTTGGGGGGCCAGGGAGGAGTGACCAGGAGCAGAGAGAGT A G MAP3K4 Ensembl:ENSG00000085511 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:161069852..161069963 26863196 MeRIP-seq:(Medium) rs932222789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840581,Human_RBP_ID_5152827,Human_RBP_ID_7569180,Human_RBP_ID_18957818,Human_RBP_ID_23294938,Human_RBP_ID_26040914 RMVar_hsa_circ_14904,RMVar_hsa_circ_113190,RMVar_hsa_circ_70888,RMVar_hsa_circ_242891,RMVar_hsa_circ_266324 103216 RMVar_ID_103216 Human_SNP_ID_304058097 m1A Human chr6 + 161077688 161077688 161077688 AAGAAGTATAAGGATTCAAAGGAAACGTAGGCAGTGAAATGGCAGGACTCGGGTGGATCAAATGT AAGAAGTATAAGGATTCAAAGGAAACGTAGGCGGTGAAATGGCAGGACTCGGGTGGATCAAATGT A G MAP3K4 Ensembl:ENSG00000085511 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:161077638..161077810 26863196 MeRIP-seq:(Medium) rs993684489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15719733 RMVar_hsa_circ_113190,RMVar_hsa_circ_70888,RMVar_hsa_circ_242891,RMVar_hsa_circ_266324,RMVar_hsa_circ_338,RMVar_hsa_circ_45713,RMVar_hsa_circ_329255,RMVar_hsa_circ_347900,RMVar_hsa_circ_366380,RMVar_hsa_circ_51262,RMVar_hsa_circ_313676,RMVar_hsa_circ_46259,RMVar_hsa_circ_20270,RMVar_hsa_circ_32187,RMVar_hsa_circ_362989,RMVar_hsa_circ_2915,RMVar_hsa_circ_374091,RMVar_hsa_circ_304344,RMVar_hsa_circ_242894,RMVar_hsa_circ_242895 103217 RMVar_ID_103217 Human_SNP_ID_304058255 m1A Human chr6 - 161078422 161078422 161078422 GTTCGCTTTCCTCTGGCTTCAGTTCAGATCCCATGGGCTTATCCTTTCAACTGCACTGCTATCAG GTTCGCTTTCCTCTGGCTTCAGTTCAGATCCCGTGGGCTTATCCTTTCAACTGCACTGCTATCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:161078373..161078559 26863196 MeRIP-seq:(Medium) rs1052018633 Functional Loss SNV dbSNP153 33..33 33 - - - 103218 RMVar_ID_103218 Human_SNP_ID_304076940 m1A Human chr6 - 161151884 161151884 161151884 ATTATCCTGCTCCCTGCAGTCCCTGCCTCTACACCGACCCTGGGCCCCAGGGCCAAGGATGCCCC ATTATCCTGCTCCCTGCAGTCCCTGCCTCTACGCCGACCCTGGGCCCCAGGGCCAAGGATGCCCC T C AGPAT4 Ensembl:ENSG00000026652 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:161151784..161151918 26863196 MeRIP-seq:(Medium) rs1333258836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242902,RMVar_hsa_circ_290655,RMVar_hsa_circ_307133,RMVar_hsa_circ_242903 103219 RMVar_ID_103219 Human_SNP_ID_304085880 m1A Human chr6 + 161186588 161186588 161186588 ACCTTCTACCCAGTCTCTCTGCCTCCAAAGTCACCCGCTCCGCATGCCAGTCTCATGCCTTGCCG ACCTTCTACCCAGTCTCTCTGCCTCCAAAGTCCCCCGCTCCGCATGCCAGTCTCATGCCTTGCCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:161186436..161186719 26863196 MeRIP-seq:(Medium) rs900654545 Functional Loss SNV dbSNP153 33..33 33 - - - 103220 RMVar_ID_103220 Human_SNP_ID_304654619 m1A Human chr6 - 163414849 163414847 163414850 GGGGCGCGGGCTGCTGGCGCCGGACGAGGAGGAGCCGGGGCCGCCGCTCGCTCGGCTGGTCGAGC GGGGCGCGGGCTGCTGGCGCCGGACGAGGAG___CCGGGGCCGCCGCTCGCTCGGCTGGTCGAGC GCTC G lnc-PRKN-23 RNACentral:URS0000D59EEE lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:163414748..163414948 26863410 MeRIP-seq:(Medium) rs891949548 Functional Loss DEL dbSNP153 32..34 33 - - - 103221 RMVar_ID_103221 Human_SNP_ID_304654621 m1A Human chr6 - 163414852 163414852 163414852 CGCGGGGCGCGGGCTGCTGGCGCCGGACGAGGAGGAGCCGGGGCCGCCGCTCGCTCGGCTGGTCG CGCGGGGCGCGGGCTGCTGGCGCCGGACGAGGGGGAGCCGGGGCCGCCGCTCGCTCGGCTGGTCG T C lnc-PRKN-23 RNACentral:URS0000D59EEE lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:163414751..163414900 26863410 MeRIP-seq:(Medium) rs1221017827 Functional Loss SNV dbSNP153 33..33 33 - - - 103222 RMVar_ID_103222 Human_SNP_ID_304654807 m1A Human chr6 - 163415174 163415174 163415174 TTTCCCCGACCATATTCCAGGCTCCGCAGCTCACTCCGCCCGCCGCCGCCGCCGCCGCCGCCGGA TTTCCCCGACCATATTCCAGGCTCCGCAGCTCCCTCCGCCCGCCGCCGCCGCCGCCGCCGCCGGA T G lnc-PRKN-23 RNACentral:URS0000D59EEE lincRNA intron GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,Wild Type chr6:163415040..163415225;chr6:163415014..163415190 26863196,26863410 MeRIP-seq:(Medium) rs773719970 Functional Loss SNV dbSNP153 33..33 33 - - - 103223 RMVar_ID_103223 Human_SNP_ID_304654821 m1A Human chr6 + 163415184 163415184 163415184 GCGGCGGCGGCGGCGGGCGGAGTGAGCTGCGGAGCCTGGAATATGGTCGGGGAAATGGAAACGAA GCGGCGGCGGCGGCGGGCGGAGTGAGCTGCGGTGCCTGGAATATGGTCGGGGAAATGGAAACGAA A T QKI Ensembl:ENSG00000112531 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:163414726..163415275 26863196 MeRIP-seq:(Medium) rs752995915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842110,Human_RBP_ID_1666807,Human_RBP_ID_2013694,Human_RBP_ID_4905642,Human_RBP_ID_5532972,Human_RBP_ID_7660872,Human_RBP_ID_8898286,Human_RBP_ID_17534680 RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 103224 RMVar_ID_103224 Human_SNP_ID_304662603 m1A Human chr6 + 163442645 163442645 163442645 CTGAAAGTTGAGTACACAGTATTTGCTAGTGGATGGAATATGAAGTGTGAGAATGGACTTGACAT CTGAAAGTTGAGTACACAGTATTTGCTAGTGGCTGGAATATGAAGTGTGAGAATGGACTTGACAT A C QKI Ensembl:ENSG00000112531 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:163442639..163442780 26863196 MeRIP-seq:(Medium) rs1290026598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15722168 RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 103225 RMVar_ID_103225 Human_SNP_ID_304662604 m1A Human chr6 + 163442645 163442645 163442645 CTGAAAGTTGAGTACACAGTATTTGCTAGTGGATGGAATATGAAGTGTGAGAATGGACTTGACAT CTGAAAGTTGAGTACACAGTATTTGCTAGTGGTTGGAATATGAAGTGTGAGAATGGACTTGACAT A T QKI Ensembl:ENSG00000112531 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:163442639..163442780 26863196 MeRIP-seq:(Medium) rs1290026598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15722168 RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 103226 RMVar_ID_103226 Human_SNP_ID_438077211 m1A Human chr10 + 75022128 75022102 75022129 GGAGGAAGAAGAGGAGGAAGAAGAGGAAGAGGATGAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG GGAGGAA___________________________GAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG AGAAGAGGAGGAAGAAGAGGAAGAGGAT A KAT6B Ensembl:ENSG00000156650 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:75021918..75022211 26863196 MeRIP-seq:(Medium) rs756289189 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_192356,Human_RBP_ID_1452973,Human_RBP_ID_4128200,Human_RBP_ID_18970086,Human_RBP_ID_22886652,Human_RBP_ID_23117785,Human_RBP_ID_24541997,Human_RBP_ID_24836360,Human_RBP_ID_26316455,Human_RBP_ID_27802161 RMVar_hsa_circ_17668,RMVar_hsa_circ_364394,RMVar_hsa_circ_57757,RMVar_hsa_circ_4471,RMVar_hsa_circ_357194 103227 RMVar_ID_103227 Human_SNP_ID_438077232 m1A Human chr10 + 75022128 75022120 75022129 GGAGGAAGAAGAGGAGGAAGAAGAGGAAGAGGATGAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG GGAGGAAGAAGAGGAGGAAGAAGAG_________GAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG GGAAGAGGAT G KAT6B Ensembl:ENSG00000156650 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:75021918..75022211 26863196 MeRIP-seq:(Medium) rs771834072 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_192356,Human_RBP_ID_1452973,Human_RBP_ID_4128200,Human_RBP_ID_18970086,Human_RBP_ID_22886652,Human_RBP_ID_23117785,Human_RBP_ID_24541997,Human_RBP_ID_24836360,Human_RBP_ID_26316455,Human_RBP_ID_27802161 RMVar_hsa_circ_17668,RMVar_hsa_circ_364394,RMVar_hsa_circ_57757,RMVar_hsa_circ_4471,RMVar_hsa_circ_357194 103228 RMVar_ID_103228 Human_SNP_ID_438077237 m1A Human chr10 + 75022128 75022123 75022129 GGAGGAAGAAGAGGAGGAAGAAGAGGAAGAGGATGAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG GGAGGAAGAAGAGGAGGAAGAAGAGGAA______GAAGAGGAGGAAGAAGAGGAAGAAGAAGAAG AGAGGAT A KAT6B Ensembl:ENSG00000156650 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:75021918..75022211 26863196 MeRIP-seq:(Medium) rs1564626372 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_192356,Human_RBP_ID_1452973,Human_RBP_ID_4128200,Human_RBP_ID_18970086,Human_RBP_ID_22886652,Human_RBP_ID_23117785,Human_RBP_ID_24541997,Human_RBP_ID_24836360,Human_RBP_ID_26316455,Human_RBP_ID_27802161 RMVar_hsa_circ_17668,RMVar_hsa_circ_364394,RMVar_hsa_circ_57757,RMVar_hsa_circ_4471,RMVar_hsa_circ_357194 103229 RMVar_ID_103229 Human_SNP_ID_438077248 m1A Human chr10 + 75022141 75022138 75022141 GAGGAAGAAGAGGAAGAGGATGAAGAGGAGGAAGAAGAGGAAGAAGAAGAAGAAGAAGAAGAAAA GAGGAAGAAGAGGAAGAGGATGAAGAGGAG___GAAGAGGAAGAAGAAGAAGAAGAAGAAGAAAA GGAA G KAT6B Ensembl:ENSG00000156650 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75021902..75022218 26863196 MeRIP-seq:(Medium) rs1000711605 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_192356,Human_RBP_ID_862482,Human_RBP_ID_1452973,Human_RBP_ID_18970086,Human_RBP_ID_22886652,Human_RBP_ID_23117785,Human_RBP_ID_24541997,Human_RBP_ID_26316455,Human_RBP_ID_27802161 Human_Splice_Rec_1148671,Human_Splice_Rec_1148731,Human_Splice_Rec_1148765,Human_Splice_Rec_1148797,Human_Splice_Rec_1148825,Human_Splice_Rec_1148859,Human_Splice_Rec_1148945,Human_Splice_Rec_1148983,Human_Splice_Rec_1149041,Human_Splice_Rec_1149111,Human_Splice_Rec_1149145,Human_Splice_Rec_1149177,Human_Splice_Rec_1149289,Human_Splice_Rec_1149389,Human_Splice_Rec_1149401 RMVar_hsa_circ_17668,RMVar_hsa_circ_364394,RMVar_hsa_circ_57757,RMVar_hsa_circ_4471,RMVar_hsa_circ_357194 103230 RMVar_ID_103230 Human_SNP_ID_438123313 m1A Human chr10 + 75210926 75210926 75210926 CAGCTAGCGGAGCGGTGGCGGCGGCCCCCCTCAGGACACCACCAGGTACCGCCGCGCCCGCCTCA CAGCTAGCGGAGCGGTGGCGGCGGCCCCCCTCTGGACACCACCAGGTACCGCCGCGCCCGCCTCA A T VDAC2 Ensembl:ENSG00000165637 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:75210684..75211175 26863196 MeRIP-seq:(Medium) rs1275403089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382941,Human_RBP_ID_805309,Human_RBP_ID_863678,Human_RBP_ID_4136382,Human_RBP_ID_9320621,Human_RBP_ID_22640270 Human_Splice_Rec_1149653,Human_Splice_Rec_1149671,Human_Splice_Rec_1149687,Human_Splice_Rec_1149695,Human_Splice_Rec_1149707,Human_Splice_Rec_1149717,Human_Splice_Rec_1149737,Human_Splice_Rec_1149753 RMVar_hsa_circ_83688,RMVar_hsa_circ_144470 103231 RMVar_ID_103231 Human_SNP_ID_438130318 m1A Human chr10 + 75234663 75234663 75234663 TCCGGGTCGCAGCAGCTGCAGGCAGCGCTCGTAGTAGGCGGAGCAGTTCTCCTTGTCCGCATCCA TCCGGGTCGCAGCAGCTGCAGGCAGCGCTCGTCGTAGGCGGAGCAGTTCTCCTTGTCCGCATCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75234463..75234669 26863196 MeRIP-seq:(Medium) rs1226886756 Functional Loss SNV dbSNP153 33..33 33 - - - 103232 RMVar_ID_103232 Human_SNP_ID_438130326 m1A Human chr10 - 75234680 75234678 75234681 CTTCGACGTGGCCGTGGTGGATGCGGACAAGGAGAACTGCTCCGCCTACTACGAGCGCTGCCTGC CTTCGACGTGGCCGTGGTGGATGCGGACAAG___AACTGCTCCGCCTACTACGAGCGCTGCCTGC TCTC T COMTD1 Ensembl:ENSG00000165644 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:75234563..75234712 32194978 MeRIP-seq:(Medium) rs745662514 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_382999,Human_RBP_ID_22886760 Human_Splice_Rec_1149796,Human_Splice_Rec_1149797,Human_Splice_Rec_1149802,Human_Splice_Rec_1149803,Human_Splice_Rec_1149808,Human_Splice_Rec_1149809,Human_Splice_Rec_1149816,Human_Splice_Rec_1149817,Human_Splice_Rec_1149826,Human_Splice_Rec_1149827,Human_Splice_Rec_1149834 RMVar_hsa_circ_144477,RMVar_hsa_circ_122572 103233 RMVar_ID_103233 Human_SNP_ID_438130498 m1A Human chr10 - 75235100 75235100 75235100 CGCGGACGGGCGCGTGGTGACCTGCGAGGTGGACGCGCAGCCCCCGGAGCTGGGACGGCCCCTGT CGCGGACGGGCGCGTGGTGACCTGCGAGGTGGTCGCGCAGCCCCCGGAGCTGGGACGGCCCCTGT T A COMTD1 Ensembl:ENSG00000165644 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:75234661..75235537 26863410 MeRIP-seq:(Medium) rs1036759899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225380,Human_RBP_ID_383006,Human_RBP_ID_861592,Human_RBP_ID_18187958,Human_RBP_ID_18970878,Human_RBP_ID_22431742,Human_RBP_ID_23206483 Human_Splice_Rec_1149792,Human_Splice_Rec_1149793,Human_Splice_Rec_1149800,Human_Splice_Rec_1149812,Human_Splice_Rec_1149813,Human_Splice_Rec_1149822,Human_Splice_Rec_1149823,Human_Splice_Rec_1149830,Human_Splice_Rec_1149831 RMVar_hsa_circ_144477,RMVar_hsa_circ_122572,RMVar_hsa_circ_265192 103234 RMVar_ID_103234 Human_SNP_ID_438130517 m1A Human chr10 + 75235148 75235148 75235148 CCACGCGCCCGTCCGCGGGCAGCGCCAGGGCCAGGGCCAGGGCGGAGTAGCCCGTGAAGGTGCCT CCACGCGCCCGTCCGCGGGCAGCGCCAGGGCCCGGGCCAGGGCGGAGTAGCCCGTGAAGGTGCCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75235126..75235150 26863196 MeRIP-seq:(Medium) rs1337034599 Functional Loss SNV dbSNP153 33..33 33 - - - 103235 RMVar_ID_103235 Human_SNP_ID_438130723 m1A Human chr10 - 75235710 75235710 75235710 GAGGCGGTGCCCCCCATGGCGAGGCCGGCGAGAGCAGTGCCTGCTTCCCCCCGAGGACAGCCGCC GAGGCGGTGCCCCCCATGGCGAGGCCGGCGAGGGCAGTGCCTGCTTCCCCCCGAGGACAGCCGCC T C COMTD1 Ensembl:ENSG00000165644 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75235609..75235780 26863196 MeRIP-seq:(Medium) rs558946859 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_383008,Human_RBP_ID_19045471 Human_Splice_Rec_1149788,Human_Splice_Rec_1149789,Human_Splice_Rec_1149820,Human_Splice_Rec_1149835 RMVar_hsa_circ_144477,RMVar_hsa_circ_122572 103236 RMVar_ID_103236 Human_SNP_ID_438130839 m1A Human chr10 - 75235869 75235869 75235869 GTGCCCGCCGCGCTGGCCCTGGGCTCAGCCGCACTGGGCGCCGCCTTCGCCACTGGCCTCTTCCT GTGCCCGCCGCGCTGGCCCTGGGCTCAGCCGCGCTGGGCGCCGCCTTCGCCACTGGCCTCTTCCT T C COMTD1 Ensembl:ENSG00000165644 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr10:75235676..75235950;chr10:75235651..75235981 26863410 MeRIP-seq:(Medium) rs994458857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225383,Human_RBP_ID_383010,Human_RBP_ID_4128465,Human_RBP_ID_5110213 Human_Splice_Rec_1149787,Human_Splice_Rec_1149805,Human_Splice_Rec_1149819 RMVar_hsa_circ_144477,RMVar_hsa_circ_122572 103237 RMVar_ID_103237 Human_SNP_ID_438168588 m1A Human chr10 - 75398823 75398823 75398823 CGCCTGGCGCCCCCGTGCCGGTGCCCGCCGCCACCGGACCGTACTACTCCCCCTACGCCCTCTAC CGCCTGGCGCCCCCGTGCCGGTGCCCGCCGCCGCCGGACCGTACTACTCCCCCTACGCCCTCTAC T C AC010997.3,ZNF503 Ensembl:ENSG00000270087,Ensembl:ENSG00000165655 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75398775..75398981 26863196 MeRIP-seq:(Medium) rs1315244309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863217,Human_RBP_ID_5165320,Human_RBP_ID_6027601,Human_RBP_ID_11434317,Human_RBP_ID_17344875,Human_RBP_ID_26882544,Human_RBP_ID_27195309,Human_RBP_ID_27408322 103238 RMVar_ID_103238 Human_SNP_ID_438168657 m1A Human chr10 + 75398958 75398958 75398958 CGCCAGCGTCCCAGGGCTGCCCGGTGCGCCCGAGGTGGGGATGTGCATGTGGCAAGCCATGGCGG CGCCAGCGTCCCAGGGCTGCCCGGTGCGCCCGCGGTGGGGATGTGCATGTGGCAAGCCATGGCGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75398909..75398999 26863196 MeRIP-seq:(Medium) rs954773365 Functional Loss SNV dbSNP153 33..33 33 - - - 103239 RMVar_ID_103239 Human_SNP_ID_438168947 m1A Human chr10 + 75399487 75399487 75399487 GGGCTGGAGCCGGCCGGCTTACTGCAGCCCAGAGACCCGGCCGCGGCCGCCGCCAGCTGCGCCCC GGGCTGGAGCCGGCCGGCTTACTGCAGCCCAGCGACCCGGCCGCGGCCGCCGCCAGCTGCGCCCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:75399401..75400327 26863410 MeRIP-seq:(Medium) rs981035941 Functional Loss SNV dbSNP153 33..33 33 - - - 103240 RMVar_ID_103240 Human_SNP_ID_438169854 m1A Human chr10 - 75401201 75401201 75401201 TCTGACCCCCTGCGCCAGGCCAACCGCCTGCCAATCAAGGTGCTGAAGATGCTGACGGCACGAAC TCTGACCCCCTGCGCCAGGCCAACCGCCTGCCGATCAAGGTGCTGAAGATGCTGACGGCACGAAC T C AC010997.3,ZNF503 Ensembl:ENSG00000270087,Ensembl:ENSG00000165655 lincRNA,Protein coding exon,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75401151..75401366 26863196 MeRIP-seq:(Medium) rs749654342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225613,Human_RBP_ID_985427,Human_RBP_ID_1450327,Human_RBP_ID_4136858,Human_RBP_ID_5459488,Human_RBP_ID_17783078,Human_RBP_ID_22156062,Human_RBP_ID_22490352,Human_RBP_ID_22788791,Human_RBP_ID_27195343,Human_RBP_ID_27407312 Human_Splice_Rec_1149985,Human_Splice_Rec_1149997 103241 RMVar_ID_103241 Human_SNP_ID_438169885 m1A Human chr10 + 75401241 75401241 75401241 GGTTGGCCTGGCGCAGGGGGTCAGAGGGGGGCACGGCGTGCACAAAAGGCTTGGTGCTGCCGGCC GGTTGGCCTGGCGCAGGGGGTCAGAGGGGGGCTCGGCGTGCACAAAAGGCTTGGTGCTGCCGGCC A T ZNF503-AS2 RNACentral:URS00008B2657 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75401191..75401353 26863196 MeRIP-seq:(Medium) rs985420192 Functional Loss SNV dbSNP153 33..33 33 - - - 103242 RMVar_ID_103242 Human_SNP_ID_438170097 m1A Human chr10 + 75401464 75401464 75401464 CGCATGGGAGCAGCGGGGGGGAGGGCTCCGGGAGGCGCGGGGCGGGCTCGGGGCTGCGCGCTCGC CGCATGGGAGCAGCGGGGGGGAGGGCTCCGGGTGGCGCGGGGCGGGCTCGGGGCTGCGCGCTCGC A T ZNF503-AS2 RNACentral:URS00008B2657 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:75401337..75401491 26863410 MeRIP-seq:(Medium) rs1271636751 Functional Loss SNV dbSNP153 33..33 33 - - - 103243 RMVar_ID_103243 Human_SNP_ID_438170142 m1A Human chr10 - 75401564 75401545 75401565 CCAGGATTACTCGCGTCTGGCTCCAGGCGCCGAGAAGGCGCGCTGGGCGCCCGTGGCCGCCGCGC CCAGGATTACTCGCGTCTGGCTCCAGGCGCC____________________CGTGGCCGCCGCGC GGGCGCCCAGCGCGCCTTCTC G ZNF503 Ensembl:ENSG00000165655 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:75401516..75401869 26863196 MeRIP-seq:(Medium) rs756340568 Functional Loss DEL dbSNP153 32..51 33 - - - Human_RBP_ID_1450330,Human_RBP_ID_4136859,Human_RBP_ID_5415509,Human_RBP_ID_5435698,Human_RBP_ID_5459503,Human_RBP_ID_5488536,Human_RBP_ID_6003314,Human_RBP_ID_17783081,Human_RBP_ID_26882594 103244 RMVar_ID_103244 Human_SNP_ID_438170169 m1A Human chr10 + 75401606 75401606 75401606 GAGCCAGACGCGAGTAATCCTGGGTGGCCCGCAGCGGAGCCGTGGCCGGGCTAGAGGAGCCGGCT GAGCCAGACGCGAGTAATCCTGGGTGGCCCGCGGCGGAGCCGTGGCCGGGCTAGAGGAGCCGGCT A G ZNF503-AS2 Ensembl:ENSG00000237149 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:75401555..75401655 32194978 MeRIP-seq:(Medium) rs761931033 Functional Loss SNV dbSNP153 33..33 33 - - - 103245 RMVar_ID_103245 Human_SNP_ID_438170170 m1A Human chr10 + 75401606 75401606 75401606 GAGCCAGACGCGAGTAATCCTGGGTGGCCCGCAGCGGAGCCGTGGCCGGGCTAGAGGAGCCGGCT GAGCCAGACGCGAGTAATCCTGGGTGGCCCGCTGCGGAGCCGTGGCCGGGCTAGAGGAGCCGGCT A T ZNF503-AS2 Ensembl:ENSG00000237149 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:75401555..75401655 32194978 MeRIP-seq:(Medium) rs761931033 Functional Loss SNV dbSNP153 33..33 33 - - - 103246 RMVar_ID_103246 Human_SNP_ID_438170290 m1A Human chr10 - 75401869 75401869 75401869 AGCGGCGGCGGCGGCGGCGCGGGACGCGTCACATCCCCTTGACCCTCCAATCACCTCGGGCTCCC AGCGGCGGCGGCGGCGGCGCGGGACGCGTCACGTCCCCTTGACCCTCCAATCACCTCGGGCTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75401818..75401919 26863196 MeRIP-seq:(Medium) rs1415204809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4128609 103247 RMVar_ID_103247 Human_SNP_ID_438177725 m1A Human chr10 - 75431673 75431673 75431673 GCGCGCGGGACGGAGCGCGGGGGCGCGGCGGCAGCAGCGGGGAGCGCGGCAGGGGAGCGCGGCGG GCGCGCGGGACGGAGCGCGGGGGCGCGGCGGCGGCAGCGGGGAGCGCGGCAGGGGAGCGCGGCGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75431641..75431724 26863196 MeRIP-seq:(Medium) rs1196861702 Functional Loss SNV dbSNP153 33..33 33 - - - 103248 RMVar_ID_103248 Human_SNP_ID_438734320 m1A Human chr10 - 77791988 77791988 77791988 GTGTTGGTTTCGTTCCCGTCTTCAGCAAAACGACCTTGGAACCTCAATGGGGGCTGCTTTGCTTT GTGTTGGTTTCGTTCCCGTCTTCAGCAAAACGGCCTTGGAACCTCAATGGGGGCTGCTTTGCTTT T C DLG5 Ensembl:ENSG00000151208 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77791939..77792422 26863196 MeRIP-seq:(Medium) rs1258337306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1160033,Human_RBP_ID_5459526,Human_RBP_ID_8763425,Human_RBP_ID_18598847 103249 RMVar_ID_103249 Human_SNP_ID_438739453 m1A Human chr10 - 77811985 77811985 77811985 CGCGGCTCATCATCGGGCAGCAGTGTGATACCATCACCATCCTGGCCCAGTACAACCCCCACGTG CGCGGCTCATCATCGGGCAGCAGTGTGATACCGTCACCATCCTGGCCCAGTACAACCCCCACGTG T C DLG5 Ensembl:ENSG00000151208 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:77811864..77812053 26863196 MeRIP-seq:(Medium) rs1214562065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3358499,Human_RBP_ID_5164121,Human_RBP_ID_8763450,Human_RBP_ID_17783279,Human_RBP_ID_18970888 Human_Splice_Rec_1154250,Human_Splice_Rec_1154251,Human_Splice_Rec_1154290,Human_Splice_Rec_1154291,Human_Splice_Rec_1154350,Human_Splice_Rec_1154351,Human_Splice_Rec_1154380,Human_Splice_Rec_1154381,Human_Splice_Rec_1154412,Human_Splice_Rec_1154413,Human_Splice_Rec_1154472,Human_Splice_Rec_1154473,Human_Splice_Rec_1154486,Human_Splice_Rec_1154487 RMVar_hsa_circ_37984,RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_60039,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_99757,RMVar_hsa_circ_94488,RMVar_hsa_circ_144522,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525 103250 RMVar_ID_103250 Human_SNP_ID_438740806 m1A Human chr10 + 77816631 77816631 77816631 GGCAATGTGGAGGCTGAGGTCTGGGACTGGCTACAAGAGGACAGGGTGTCGATGTTCAGGGGTGA GGCAATGTGGAGGCTGAGGTCTGGGACTGGCTCCAAGAGGACAGGGTGTCGATGTTCAGGGGTGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77816520..77816701 26863196 MeRIP-seq:(Medium) rs775429189 Functional Loss SNV dbSNP153 33..33 33 - - - 103251 RMVar_ID_103251 Human_SNP_ID_438740816 m1A Human chr10 - 77816647 77816647 77816647 CAGCACTCCTCCACAGTCACCCCTGAACATCGACACCCTGTCCTCTTGTAGCCAGTCCCAGACCT CAGCACTCCTCCACAGTCACCCCTGAACATCGTCACCCTGTCCTCTTGTAGCCAGTCCCAGACCT T A DLG5 Ensembl:ENSG00000151208 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:77816601..77816675 26863196 MeRIP-seq:(Medium) rs1381202347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3358502,Human_RBP_ID_3938413,Human_RBP_ID_11437751 Human_Splice_Rec_1154246,Human_Splice_Rec_1154247,Human_Splice_Rec_1154286,Human_Splice_Rec_1154287,Human_Splice_Rec_1154346,Human_Splice_Rec_1154347,Human_Splice_Rec_1154376,Human_Splice_Rec_1154377,Human_Splice_Rec_1154408,Human_Splice_Rec_1154409,Human_Splice_Rec_1154468,Human_Splice_Rec_1154469,Human_Splice_Rec_1154504,Human_Splice_Rec_1154505 RMVar_hsa_circ_5754,RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_99757,RMVar_hsa_circ_94488,RMVar_hsa_circ_144522,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525,RMVar_hsa_circ_101502,RMVar_hsa_circ_144527 103252 RMVar_ID_103252 Human_SNP_ID_438742171 m1A Human chr10 - 77821276 77821276 77821276 AGCCCATGCACGCATCACCCCCTCGCAAGGCCAGGGTCCGCATTGCTTCCAGCTACTACCCTGAA AGCCCATGCACGCATCACCCCCTCGCAAGGCCGGGGTCCGCATTGCTTCCAGCTACTACCCTGAA T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77821228..77821723 26863196 MeRIP-seq:(Medium) rs1196872311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2222,Human_RBP_ID_5459691,Human_RBP_ID_11437785,Human_RBP_ID_23206485 RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_99757,RMVar_hsa_circ_94488,RMVar_hsa_circ_144522,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525,RMVar_hsa_circ_101502,RMVar_hsa_circ_105290,RMVar_hsa_circ_144527,RMVar_hsa_circ_144528 103253 RMVar_ID_103253 Human_SNP_ID_438742220 m1A Human chr10 + 77821360 77821360 77821360 GGGCAGGGCGCTCGGGGGACTAGTGGATGGGGAGCTGCCCACCAGAGTGGCTTCTGACTCGGAGC GGGCAGGGCGCTCGGGGGACTAGTGGATGGGGTGCTGCCCACCAGAGTGGCTTCTGACTCGGAGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:77821309..77821500 26863196 MeRIP-seq:(Medium) rs757061091 Functional Loss SNV dbSNP153 33..33 33 - - - 103254 RMVar_ID_103254 Human_SNP_ID_438742229 m1A Human chr10 - 77821386 77821386 77821386 TAAGTTCCAGCACAGGCTGGAGACTAGCTCCGAGTCAGAAGCCACTCTGGTGGGCAGCTCCCCAT TAAGTTCCAGCACAGGCTGGAGACTAGCTCCGGGTCAGAAGCCACTCTGGTGGGCAGCTCCCCAT T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:77821376..77821400 26863196 MeRIP-seq:(Medium) rs1568149634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1450470 Human_miRNA_ID_2453972 RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_99757,RMVar_hsa_circ_94488,RMVar_hsa_circ_144522,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525,RMVar_hsa_circ_101502,RMVar_hsa_circ_105290,RMVar_hsa_circ_144527,RMVar_hsa_circ_144528 103255 RMVar_ID_103255 Human_SNP_ID_438744741 m1A Human chr10 - 77830824 77830824 77830824 AGTTGGAAAAGGAGGCCCGGTTCCGACAGCTGATGGCCCACAGCTCCCACGACTCGGCCATTGAC AGTTGGAAAAGGAGGCCCGGTTCCGACAGCTGGTGGCCCACAGCTCCCACGACTCGGCCATTGAC T C DLG5 Ensembl:ENSG00000151208 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77830720..77830912 26863196 MeRIP-seq:(Medium) rs543304082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9274196,Human_RBP_ID_18970101 Human_Splice_Rec_1154270,Human_Splice_Rec_1154271,Human_Splice_Rec_1154326,Human_Splice_Rec_1154327,Human_Splice_Rec_1154448,Human_Splice_Rec_1154449 RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_94488,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525,RMVar_hsa_circ_101502,RMVar_hsa_circ_105290,RMVar_hsa_circ_144527,RMVar_hsa_circ_144528,RMVar_hsa_circ_337437,RMVar_hsa_circ_40544,RMVar_hsa_circ_97814,RMVar_hsa_circ_144530 103256 RMVar_ID_103256 Human_SNP_ID_438745542 m1A Human chr10 + 77834030 77834028 77834030 ACCGCACGGTCCCGCTCCCGCCTCAGGTTGTCACACAGTGTCCTGGTGGAAGGAGCAGAGGACAA ACCGCACGGTCCCGCTCCCGCCTCAGGTTGT__CACAGTGTCCTGGTGGAAGGAGCAGAGGACAA TCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77833864..77834086 26863196 MeRIP-seq:(Medium) rs1564528861 Functional Loss DEL dbSNP153 32..33 33 - - - 103257 RMVar_ID_103257 Human_SNP_ID_438745543 m1A Human chr10 + 77834030 77834030 77834030 ACCGCACGGTCCCGCTCCCGCCTCAGGTTGTCACACAGTGTCCTGGTGGAAGGAGCAGAGGACAA ACCGCACGGTCCCGCTCCCGCCTCAGGTTGTCGCACAGTGTCCTGGTGGAAGGAGCAGAGGACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77833864..77834086 26863196 MeRIP-seq:(Medium) rs1354518278 Functional Loss SNV dbSNP153 33..33 33 - - - 103258 RMVar_ID_103258 Human_SNP_ID_438747519 m1A Human chr10 + 77841835 77841835 77841835 ACACCACGCACTCTGCAGCCCCTCTTCCCGGGATGCTGTAGGAGAGGCTGAAAGCCAGCCACCGG ACACCACGCACTCTGCAGCCCCTCTTCCCGGGGTGCTGTAGGAGAGGCTGAAAGCCAGCCACCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77841831..77842226 26863196 MeRIP-seq:(Medium) rs749088137 Functional Loss SNV dbSNP153 33..33 33 - - - 103259 RMVar_ID_103259 Human_SNP_ID_438748027 m1A Human chr10 - 77843572 77843572 77843572 AGGTACAGTGAGAAAGTCGCCATCCACAATGCAGACCTGAGCCGCCTGGAGCAGCTGGGGGAGGA AGGTACAGTGAGAAAGTCGCCATCCACAATGCGGACCTGAGCCGCCTGGAGCAGCTGGGGGAGGA T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77843523..77843599 26863196 MeRIP-seq:(Medium) rs774237321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520162,Human_RBP_ID_8763487,Human_RBP_ID_9274198,Human_RBP_ID_18188066,Human_RBP_ID_18468810,Human_RBP_ID_22708130,Human_RBP_ID_26316474,Human_RBP_ID_27407393,Human_RBP_ID_27556343,Human_RBP_ID_27802170 Human_miRNA_ID_2269468,Human_miRNA_ID_2445458,Human_miRNA_ID_2446843 RMVar_hsa_circ_126566,RMVar_hsa_circ_94488,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144525,RMVar_hsa_circ_8513,RMVar_hsa_circ_97814,RMVar_hsa_circ_144530,RMVar_hsa_circ_112890,RMVar_hsa_circ_144531 103260 RMVar_ID_103260 Human_SNP_ID_438750681 m1A Human chr10 - 77854316 77854316 77854316 GACTATGAGAGGCTGAAGATCCAGTGCGTGCGAGCCATGTCGGACCTGCAGAGCCTGCAGAACCA GACTATGAGAGGCTGAAGATCCAGTGCGTGCGGGCCATGTCGGACCTGCAGAGCCTGCAGAACCA T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77854192..77854408 26863196 MeRIP-seq:(Medium) rs942586717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8763492,Human_RBP_ID_26882767 Human_Splice_Rec_1154314,Human_Splice_Rec_1154315,Human_Splice_Rec_1154434,Human_Splice_Rec_1154435 Human_miRNA_ID_2395358 RMVar_hsa_circ_126566,RMVar_hsa_circ_94488,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144525,RMVar_hsa_circ_97814,RMVar_hsa_circ_144530,RMVar_hsa_circ_112890,RMVar_hsa_circ_296916,RMVar_hsa_circ_144531,RMVar_hsa_circ_324307,RMVar_hsa_circ_291399,RMVar_hsa_circ_144533,RMVar_hsa_circ_144534,RMVar_hsa_circ_144535 103261 RMVar_ID_103261 Human_SNP_ID_438754921 m1A Human chr10 + 77872295 77872295 77872295 TCTTCAAATCGTCTCTCTCCTCCCCTGTGGCAAGTTTCCACTGTTAATTAAGCTTGGCAGATGCC TCTTCAAATCGTCTCTCTCCTCCCCTGTGGCAGGTTTCCACTGTTAATTAAGCTTGGCAGATGCC A G lnc-RPS24-6 RNACentral:URS00008B24C9 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77872287..77872458 26863196 MeRIP-seq:(Medium) rs1474435906 Functional Loss SNV dbSNP153 33..33 33 - - - 103262 RMVar_ID_103262 Human_SNP_ID_438760396 m1A Human chr10 - 77894735 77894735 77894735 TTTGAGTTTTTCTGGATGGGCAGAGGTGGGGAAGGGGTACGCTGGGAATCAGGGAGCAGAAAAGG TTTGAGTTTTTCTGGATGGGCAGAGGTGGGGATGGGGTACGCTGGGAATCAGGGAGCAGAAAAGG T A DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77894732..77894943 26863196 MeRIP-seq:(Medium) rs147755404 Functional Loss SNV dbSNP153 33..33 33 - - - 103263 RMVar_ID_103263 Human_SNP_ID_438760461 m1A Human chr10 - 77895029 77895029 77895029 GCTCATCACTTTTCTTCCCTGAACCCATGTCCACCTCTCATAAGGTTGTATCGAAGTTCCAAGAA GCTCATCACTTTTCTTCCCTGAACCCATGTCCGCCTCTCATAAGGTTGTATCGAAGTTCCAAGAA T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:77895023..77895107 26863410 MeRIP-seq:(Medium) rs975339066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11438109 103264 RMVar_ID_103264 Human_SNP_ID_438768193 m1A Human chr10 - 77926412 77926412 77926412 TGCTCGGGCTGCTCGAGGCCGCGGGAGCGCTCAGTCCCGGCGAGCGGCGGCAGCTGGACGAGGAG TGCTCGGGCTGCTCGAGGCCGCGGGAGCGCTCTGTCCCGGCGAGCGGCGGCAGCTGGACGAGGAG T A DLG5 Ensembl:ENSG00000151208 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77926144..77926629 26863196 MeRIP-seq:(Medium) rs1161500117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4143775,Human_RBP_ID_9320625,Human_RBP_ID_18970900 103265 RMVar_ID_103265 Human_SNP_ID_438768455 m1A Human chr10 + 77927012 77927012 77927012 CCCAGGCTCCCGACAGCTCCGGCCCGGCTCGGAGGCCGCCTCGGCCCCCGTGCACCCCGGCCCGG CCCAGGCTCCCGACAGCTCCGGCCCGGCTCGGCGGCCGCCTCGGCCCCCGTGCACCCCGGCCCGG A C DLG5-AS1,DLG5-AS1:2,DLG5-AS1:3,DLG5-AS1:4,lnc-RPS24-14 RNACentral:URS0000759D71,RNACentral:URS00009C43DB,RNACentral:URS00008B899B,RNACentral:URS00008B9497,RNACentral:URS00008B3393 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:77926965..77927079 26863196 MeRIP-seq:(Medium) rs1330271966 Functional Loss SNV dbSNP153 33..33 33 - - - 103266 RMVar_ID_103266 Human_SNP_ID_438781633 m1A Human chr10 - 77982183 77982183 77982183 GGGCAGTCATGGCCACACACGGTGTGAAGGGCACCCGAACCACCTCCAATAACACCTATGAGGTA GGGCAGTCATGGCCACACACGGTGTGAAGGGCCCCCGAACCACCTCCAATAACACCTATGAGGTA T G POLR3A Ensembl:ENSG00000148606 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:77982173..77982279 26863410 MeRIP-seq:(Medium) rs745918351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864540,Human_RBP_ID_18970902 Human_Splice_Rec_1154519,Human_Splice_Rec_1154579 RMVar_hsa_circ_89380,RMVar_hsa_circ_80498,RMVar_hsa_circ_97515,RMVar_hsa_circ_121862,RMVar_hsa_circ_144539,RMVar_hsa_circ_144540,RMVar_hsa_circ_127006,RMVar_hsa_circ_112518,RMVar_hsa_circ_91692,RMVar_hsa_circ_144543,RMVar_hsa_circ_34301,RMVar_hsa_circ_78814,RMVar_hsa_circ_144545,RMVar_hsa_circ_144547,RMVar_hsa_circ_144548,RMVar_hsa_circ_144546,RMVar_hsa_circ_144544,RMVar_hsa_circ_349036,RMVar_hsa_circ_144549,RMVar_hsa_circ_373056,RMVar_hsa_circ_144550,RMVar_hsa_circ_288428 103267 RMVar_ID_103267 Human_SNP_ID_438781645 m1A Human chr10 - 77982211 77982211 77982211 AAGCTTCTGGTGGAAGGTGATAACCTGCGGGCAGTCATGGCCACACACGGTGTGAAGGGCACCCG AAGCTTCTGGTGGAAGGTGATAACCTGCGGGCGGTCATGGCCACACACGGTGTGAAGGGCACCCG T C POLR3A Ensembl:ENSG00000148606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77982145..77982278 26863196 MeRIP-seq:(Medium) rs146725238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27427,Human_RBP_ID_864540,Human_RBP_ID_6004919,Human_RBP_ID_18970902 Human_Splice_Rec_1154519,Human_Splice_Rec_1154579 RMVar_hsa_circ_89380,RMVar_hsa_circ_80498,RMVar_hsa_circ_97515,RMVar_hsa_circ_121862,RMVar_hsa_circ_144539,RMVar_hsa_circ_144540,RMVar_hsa_circ_127006,RMVar_hsa_circ_112518,RMVar_hsa_circ_91692,RMVar_hsa_circ_144543,RMVar_hsa_circ_34301,RMVar_hsa_circ_78814,RMVar_hsa_circ_144545,RMVar_hsa_circ_144547,RMVar_hsa_circ_144548,RMVar_hsa_circ_144546,RMVar_hsa_circ_144544,RMVar_hsa_circ_349036,RMVar_hsa_circ_144549,RMVar_hsa_circ_373056,RMVar_hsa_circ_144550,RMVar_hsa_circ_288428 103268 RMVar_ID_103268 Human_SNP_ID_438781646 m1A Human chr10 - 77982211 77982211 77982211 AAGCTTCTGGTGGAAGGTGATAACCTGCGGGCAGTCATGGCCACACACGGTGTGAAGGGCACCCG AAGCTTCTGGTGGAAGGTGATAACCTGCGGGCCGTCATGGCCACACACGGTGTGAAGGGCACCCG T G POLR3A Ensembl:ENSG00000148606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:77982145..77982278 26863196 MeRIP-seq:(Medium) rs146725238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27427,Human_RBP_ID_864540,Human_RBP_ID_6004919,Human_RBP_ID_18970902 Human_Splice_Rec_1154519,Human_Splice_Rec_1154579 RMVar_hsa_circ_89380,RMVar_hsa_circ_80498,RMVar_hsa_circ_97515,RMVar_hsa_circ_121862,RMVar_hsa_circ_144539,RMVar_hsa_circ_144540,RMVar_hsa_circ_127006,RMVar_hsa_circ_112518,RMVar_hsa_circ_91692,RMVar_hsa_circ_144543,RMVar_hsa_circ_34301,RMVar_hsa_circ_78814,RMVar_hsa_circ_144545,RMVar_hsa_circ_144547,RMVar_hsa_circ_144548,RMVar_hsa_circ_144546,RMVar_hsa_circ_144544,RMVar_hsa_circ_349036,RMVar_hsa_circ_144549,RMVar_hsa_circ_373056,RMVar_hsa_circ_144550,RMVar_hsa_circ_288428 103269 RMVar_ID_103269 Human_SNP_ID_438796698 m1A Human chr10 + 78037299 78037298 78037299 GGGGGACTGCAAAGGCCAATGTTGGTGCTGGCAAAAAGGTATAGTTCATTAAGGAAAATATAGAA GGGGGACTGCAAAGGCCAATGTTGGTGCTGGC_AAAAGGTATAGTTCATTAAGGAAAATATAGAA CA C RPS24 Ensembl:ENSG00000138326 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr10:78037198..78037343;chr10:78037208..78037337;chr10:78037200..78037333;chr10:78036082..78037439 26863196,32194978 MeRIP-seq:(Medium) rs35935709 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_27328,Human_RBP_ID_192362,Human_RBP_ID_383211,Human_RBP_ID_805302,Human_RBP_ID_863600,Human_RBP_ID_1262274,Human_RBP_ID_2245308,Human_RBP_ID_8228875,Human_RBP_ID_8992890,Human_RBP_ID_9360510,Human_RBP_ID_22884925,Human_RBP_ID_23471943,Human_RBP_ID_26315946,Human_RBP_ID_27802185 Human_Splice_Rec_1154625,Human_Splice_Rec_1154633,Human_Splice_Rec_1154651,Human_Splice_Rec_1154659,Human_Splice_Rec_1154673,Human_Splice_Rec_1154685,Human_Splice_Rec_1154695,Human_Splice_Rec_1154703,Human_Splice_Rec_1154713,Human_Splice_Rec_1154727,Human_Splice_Rec_1154739,Human_Splice_Rec_1154747 Human_miRNA_ID_2005137 RMVar_hsa_circ_103023,RMVar_hsa_circ_349816,RMVar_hsa_circ_144568,RMVar_hsa_circ_367570 103270 RMVar_ID_103270 Human_SNP_ID_438797625 m1A Human chr10 - 78040604 78040603 78040605 TGCAGCACCTTTACTCCTTCGGCTGTGAATCAAGAGAAAGAAGTTTAGTCAACAACTGCCTTTAA TGCAGCACCTTTACTCCTTCGGCTGTGAATC__GAGAAAGAAGTTTAGTCAACAACTGCCTTTAA CTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:78040601..78040675 32194978 MeRIP-seq:(Medium) rs749954054 Functional Loss DEL dbSNP153 32..33 33 - - - 103271 RMVar_ID_103271 Human_SNP_ID_438797817 m1A Human chr10 + 78041263 78041263 78041263 CAATACCGTGAAGGCAGAAGGGTTGAGGTTGCAGGAAGGAAGGGTAGTGGAATGTTTTGGAGAAA CAATACCGTGAAGGCAGAAGGGTTGAGGTTGCCGGAAGGAAGGGTAGTGGAATGTTTTGGAGAAA A C RPS24 Ensembl:ENSG00000138326 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:78041215..78041381 26863196 MeRIP-seq:(Medium) rs926621152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805513,Human_RBP_ID_2245312,Human_RBP_ID_6005237,Human_RBP_ID_9610146,Human_RBP_ID_23472005 RMVar_hsa_circ_103023,RMVar_hsa_circ_144568 103272 RMVar_ID_103272 Human_SNP_ID_439056190 m1A Human chr10 + 79069024 79069024 79069024 CCTTTTCACTGTCTGTGGACATTAAAAAAGCGAGCGGCGGCGGCGGGCGCCGGGGAGAGCGGGCG CCTTTTCACTGTCTGTGGACATTAAAAAAGCGTGCGGCGGCGGCGGGCGCCGGGGAGAGCGGGCG A T ZMIZ1 Ensembl:ENSG00000108175 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:79068976..79069244;chr10:79068983..79069286 26863196 MeRIP-seq:(Medium) rs1269214124 Functional Loss SNV dbSNP153 33..33 33 - - - 103273 RMVar_ID_103273 Human_SNP_ID_439065214 m1A Human chr10 - 79103310 79103309 79103310 TCTTCCTTACAGCTGTAAAGCTTTTCCTGTTTACAGCCCCCCACCCCAGGCATCCCCACGGCCCT TCTTCCTTACAGCTGTAAAGCTTTTCCTGTTT_CAGCCCCCCACCCCAGGCATCCCCACGGCCCT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79103301..79103431 26863196 MeRIP-seq:(Medium) rs1485835723 Functional Loss DEL dbSNP153 33..33 33 - - - 103274 RMVar_ID_103274 Human_SNP_ID_439069201 m1A Human chr10 - 79118965 79118962 79118965 GACTCAAGTCTGCTGAGAGCGTCTGGAGGAGGAGGTGGCAGCCCCAGCAGTAGTACGAAATCAGA GACTCAAGTCTGCTGAGAGCGTCTGGAGGAGG___TGGCAGCCCCAGCAGTAGTACGAAATCAGA ACCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79118877..79118967 26863196 MeRIP-seq:(Medium) rs1259049301 Functional Loss DEL dbSNP153 33..35 33 - - - 103275 RMVar_ID_103275 Human_SNP_ID_439074982 m1A Human chr10 + 79142276 79142276 79142276 ATATGAGTCGGGAAGGCAGAGAGAGGTCCCAGACTAGAGATATAAATTTGGGAGTTGTCGTGGAT ATATGAGTCGGGAAGGCAGAGAGAGGTCCCAGCCTAGAGATATAAATTTGGGAGTTGTCGTGGAT A C ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:79142261..79142421 26863196 MeRIP-seq:(Medium) rs957822771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4203,RMVar_hsa_circ_93721,RMVar_hsa_circ_144571,RMVar_hsa_circ_285670,RMVar_hsa_circ_270845,RMVar_hsa_circ_109315,RMVar_hsa_circ_144576,RMVar_hsa_circ_144577,RMVar_hsa_circ_144578,RMVar_hsa_circ_144579,RMVar_hsa_circ_117771,RMVar_hsa_circ_320236 103276 RMVar_ID_103276 Human_SNP_ID_439100491 m1A Human chr10 - 79243650 79243650 79243650 GCCGGCGGCGGCCGCGGCGAGCGACTCCGGGTAGGATTCAGCCAGCGCCGAACAAAGGCTGCGCG GCCGGCGGCGGCCGCGGCGAGCGACTCCGGGTGGGATTCAGCCAGCGCCGAACAAAGGCTGCGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79243634..79243844 26863196 MeRIP-seq:(Medium) rs1188160869 Functional Loss SNV dbSNP153 33..33 33 - - - 103277 RMVar_ID_103277 Human_SNP_ID_439108173 m1A Human chr10 + 79272728 79272728 79272728 ATGGATCGAGGTGAGGGAGTCTGGTCACAAGGATGCAGTTTGGAGAGGTGAGGGGAGCTCAGTGG ATGGATCGAGGTGAGGGAGTCTGGTCACAAGGGTGCAGTTTGGAGAGGTGAGGGGAGCTCAGTGG A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79272726..79272825 26863196 MeRIP-seq:(Medium) rs1308666204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93721,RMVar_hsa_circ_144571,RMVar_hsa_circ_109315,RMVar_hsa_circ_144578,RMVar_hsa_circ_123208,RMVar_hsa_circ_108486,RMVar_hsa_circ_144581,RMVar_hsa_circ_3958,RMVar_hsa_circ_144582 103278 RMVar_ID_103278 Human_SNP_ID_439117183 m1A Human chr10 + 79304119 79304119 79304119 AGACGGCCATCAAGGTGTCTCTGAAGTGCCCCATCACATTCCGGCGCATCCAGCTGCCTGCTCGA AGACGGCCATCAAGGTGTCTCTGAAGTGCCCCGTCACATTCCGGCGCATCCAGCTGCCTGCTCGA A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:79300856..79305562 32194978 MeRIP-seq:(Medium) rs768930838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18599095 Human_Splice_Rec_1154945,Human_Splice_Rec_1154993 RMVar_hsa_circ_53288,RMVar_hsa_circ_19866 103279 RMVar_ID_103279 Human_SNP_ID_439119231 m1A Human chr10 + 79311023 79311023 79311023 CCAGCAGCCAGTCAGGGCCTCCATTACATCACAGTGGGGCTCCTCCTCCTCCTCCTTCCCAGCCT CCAGCAGCCAGTCAGGGCCTCCATTACATCACTGTGGGGCTCCTCCTCCTCCTCCTTCCCAGCCT A T ZMIZ1 Ensembl:ENSG00000108175 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:79310972..79311079 26863196 MeRIP-seq:(Medium) rs202180044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17230151,Human_RBP_ID_17462129,Human_RBP_ID_18931689 Human_Splice_Rec_1154954,Human_Splice_Rec_1154996 RMVar_hsa_circ_87576,RMVar_hsa_circ_290632,RMVar_hsa_circ_144587,RMVar_hsa_circ_144588 103280 RMVar_ID_103280 Human_SNP_ID_439128653 m1A Human chr10 + 79347536 79347536 79347536 GTTCTGTGTTCTCCCCGCCCGTGTCCCGCCCGACCCGCGCCCGCGATGCTGGCGCTGCGCTGCGG GTTCTGTGTTCTCCCCGCCCGTGTCCCGCCCGCCCCGCGCCCGCGATGCTGGCGCTGCGCTGCGG A C PPIF Ensembl:ENSG00000108179 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:79347476..79349098;chr10:79347476..79347700;chr10:79347476..79347675 26863196 MeRIP-seq:(Medium) rs937131111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383349,Human_RBP_ID_748535,Human_RBP_ID_4129492,Human_RBP_ID_5313061,Human_RBP_ID_9320633,Human_RBP_ID_22432093,Human_RBP_ID_22532228 103281 RMVar_ID_103281 Human_SNP_ID_439128676 m1A Human chr10 - 79347586 79347586 79347586 GGCGCAGCGGCACGGAGCGCGGGACGGAGAGCAGGCCGAGCCAGCGGGAGCCGCAGCGCAGCGCC GGCGCAGCGGCACGGAGCGCGGGACGGAGAGCTGGCCGAGCCAGCGGGAGCCGCAGCGCAGCGCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr10:79347499..79347670;chr10:79347451..79349755 26863196,26863410 MeRIP-seq:(Medium) rs1273078438 Functional Loss SNV dbSNP153 33..33 33 - - - 103282 RMVar_ID_103282 Human_SNP_ID_439128693 m1A Human chr10 + 79347643 79347643 79347643 GCTGCGCCTCCCCGCGGCCCGCGCCTGCAGCAAGGGCTCCGGCGACCCGTCCTCTTCCTCCTCCT GCTGCGCCTCCCCGCGGCCCGCGCCTGCAGCAGGGGCTCCGGCGACCCGTCCTCTTCCTCCTCCT A G PPIF Ensembl:ENSG00000108179 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:79347476..79347725 26863196 MeRIP-seq:(Medium) rs1427915489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225762,Human_RBP_ID_1160074,Human_RBP_ID_4129492,Human_RBP_ID_5313061,Human_RBP_ID_8244699,Human_RBP_ID_9320634,Human_RBP_ID_22431750 103283 RMVar_ID_103283 Human_SNP_ID_439129463 m1A Human chr10 - 79350555 79350555 79350555 TGTTCACCCCGTATCCAGGCTTCGCCGCACATAGACGTCCAGTCCCAACCCGCTGCCACTTACCA TGTTCACCCCGTATCCAGGCTTCGCCGCACATGGACGTCCAGTCCCAACCCGCTGCCACTTACCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79350547..79350758 26863196 MeRIP-seq:(Medium) rs1021143533 Functional Loss SNV dbSNP153 33..33 33 - - - 103284 RMVar_ID_103284 Human_SNP_ID_439129895 m1A Human chr10 - 79352305 79352305 79352305 CATTAGCCATGGACAGGACACCTGCAAAAACCAGCAGGGCTGAGCCACGCTGCCCCTGGAGGCAC CATTAGCCATGGACAGGACACCTGCAAAAACCGGCAGGGCTGAGCCACGCTGCCCCTGGAGGCAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr10:79352301..79352400;chr10:79352301..79352350 32194978 MeRIP-seq:(Medium) rs370310037 Functional Loss SNV dbSNP153 33..33 33 - - - 103285 RMVar_ID_103285 Human_SNP_ID_439130341 m1A Human chr10 + 79353956 79353956 79353956 CCTGAAACGATACGTGTGCCCACTCCACTGTCACAGTGTGCCTGAGGAAGGCTGCTAGGGATGTT CCTGAAACGATACGTGTGCCCACTCCACTGTCGCAGTGTGCCTGAGGAAGGCTGCTAGGGATGTT A G PPIF Ensembl:ENSG00000108179 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:79353851..79354025 32194978 MeRIP-seq:(Medium) rs1268316916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383362,Human_RBP_ID_4143894,Human_RBP_ID_8340186,Human_RBP_ID_17461185,Human_RBP_ID_17648291,Human_RBP_ID_23206486,Human_RBP_ID_23472556,Human_RBP_ID_26397044,Human_RBP_ID_27195619 Human_miRNA_ID_1708717,Human_miRNA_ID_2877356,Human_miRNA_ID_2998712 RMVar_hsa_circ_101125,RMVar_hsa_circ_119607,RMVar_hsa_circ_144590,RMVar_hsa_circ_144591 103286 RMVar_ID_103286 Human_SNP_ID_439139947 m1A Human chr10 - 79391997 79391997 79391997 GACTGGGTGGAGTCTGGGAGCCAGTGGAATGGAAGGAGAGAACGAGGGGGCAGAGATGGGTGGTT GACTGGGTGGAGTCTGGGAGCCAGTGGAATGGGAGGAGAGAACGAGGGGGCAGAGATGGGTGGTT T C ZCCHC24 Ensembl:ENSG00000165424 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79391954..79392181 26863196 MeRIP-seq:(Medium) rs1290243258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172251 103287 RMVar_ID_103287 Human_SNP_ID_439139954 m1A Human chr10 + 79392039 79392039 79392039 TGGCTCCCAGACTCCACCCAGTCCACAGGCCCACCCGGCCTCCCTCTCCACCGGTCCCGTCTAGC TGGCTCCCAGACTCCACCCAGTCCACAGGCCCCCCCGGCCTCCCTCTCCACCGGTCCCGTCTAGC A C AL133481.1 Ensembl:ENSG00000235426 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:79391991..79392169 26863196 MeRIP-seq:(Medium) rs895863617 Functional Loss SNV dbSNP153 33..33 33 - - - 103288 RMVar_ID_103288 Human_SNP_ID_439146074 m1A Human chr10 + 79418499 79418499 79418499 AGACTTGTGCCAGGACCGGCCCTGGGCTAGGCACGACTCACCAAGGCAGGAGCACATGGGGCATA AGACTTGTGCCAGGACCGGCCCTGGGCTAGGCTCGACTCACCAAGGCAGGAGCACATGGGGCATA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:79418378..79418507 26863196 MeRIP-seq:(Medium) rs934471036 Functional Loss SNV dbSNP153 33..33 33 - - - 103289 RMVar_ID_103289 Human_SNP_ID_439152997 m1A Human chr10 - 79445571 79445558 79445572 GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCAGGGCGCGGGGCGATCACCGTCGGGGCTCGGGA GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCG______________ATCACCGTCGGGGCTCGGGA TCGCCCCGCGCCCTG T ZCCHC24 Ensembl:ENSG00000165424 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79445319..79445606 26863196 MeRIP-seq:(Medium) rs935167526 Functional Loss DEL dbSNP153 32..45 33 - - - Human_RBP_ID_4136870,Human_RBP_ID_9320637 RMVar_hsa_circ_269618 103290 RMVar_ID_103290 Human_SNP_ID_439153005 m1A Human chr10 - 79445571 79445571 79445571 GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCAGGGCGCGGGGCGATCACCGTCGGGGCTCGGGA GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCTGGGCGCGGGGCGATCACCGTCGGGGCTCGGGA T A ZCCHC24 Ensembl:ENSG00000165424 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79445319..79445606 26863196 MeRIP-seq:(Medium) rs878898443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136870,Human_RBP_ID_9320637 RMVar_hsa_circ_269618 103291 RMVar_ID_103291 Human_SNP_ID_439153006 m1A Human chr10 - 79445571 79445571 79445571 GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCAGGGCGCGGGGCGATCACCGTCGGGGCTCGGGA GCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCGGGGCGCGGGGCGATCACCGTCGGGGCTCGGGA T C ZCCHC24 Ensembl:ENSG00000165424 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79445319..79445606 26863196 MeRIP-seq:(Medium) rs878898443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136870,Human_RBP_ID_9320637 RMVar_hsa_circ_269618 103292 RMVar_ID_103292 Human_SNP_ID_439153010 m1A Human chr10 - 79445585 79445585 79445585 GGGAGGCGGCGGCAGCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCAGGGCGCGGGGCGATCACC GGGAGGCGGCGGCAGCGGCAGCGGCTGCGGGCTGCGCGCGGGGCGCAGGGCGCGGGGCGATCACC T A ZCCHC24 Ensembl:ENSG00000165424 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79445455..79445594 26863196 MeRIP-seq:(Medium) rs906623264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136870,Human_RBP_ID_9320637 RMVar_hsa_circ_269618 103293 RMVar_ID_103293 Human_SNP_ID_439153011 m1A Human chr10 - 79445585 79445585 79445585 GGGAGGCGGCGGCAGCGGCAGCGGCTGCGGGCAGCGCGCGGGGCGCAGGGCGCGGGGCGATCACC GGGAGGCGGCGGCAGCGGCAGCGGCTGCGGGCGGCGCGCGGGGCGCAGGGCGCGGGGCGATCACC T C ZCCHC24 Ensembl:ENSG00000165424 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79445455..79445594 26863196 MeRIP-seq:(Medium) rs906623264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136870,Human_RBP_ID_9320637 RMVar_hsa_circ_269618 103294 RMVar_ID_103294 Human_SNP_ID_439170686 m1A Human chr10 + 79513023 79513022 79513024 CCCTGAGGGAGACCTTGGCAAGGAGATTGAGCAGAAGTACGACTGTGGAGAAGAGATCCTGATCA CCCTGAGGGAGACCTTGGCAAGGAGATTGAGC__AAGTACGACTGTGGAGAAGAGATCCTGATCA CAG C EIF5AL1 Ensembl:ENSG00000253626 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:79513001..79513075 26863196 MeRIP-seq:(Medium) rs556129564 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_107960,Human_RBP_ID_1450670,Human_RBP_ID_4143943,Human_RBP_ID_5545884,Human_RBP_ID_11440844,Human_RBP_ID_23472643,Human_RBP_ID_26399917 103295 RMVar_ID_103295 Human_SNP_ID_439170711 m1A Human chr10 + 79513070 79513070 79513070 GAGAAGAGATCCTGATCACGGTGCTGTCTGCCATGACAGAGGAGGCAGCTGTTGCAATCAAGGCC GAGAAGAGATCCTGATCACGGTGCTGTCTGCCGTGACAGAGGAGGCAGCTGTTGCAATCAAGGCC A G EIF5AL1 Ensembl:ENSG00000253626 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs766634397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_107960 103296 RMVar_ID_103296 Human_SNP_ID_439171888 m1A Human chr10 - 79517950 79517950 79517950 ATTTTTTTTTTCTCATCAGTTATTGTTAGTGTATTTTATGTGTGGCACAAGACAATTCTCCTTCT ATTTTTTTTTTCTCATCAGTTATTGTTAGTGTTTTTTATGTGTGGCACAAGACAATTCTCCTTCT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:79517921..79518048 26863196 MeRIP-seq:(Medium) rs1400098488 Functional Loss SNV dbSNP153 33..33 33 - - - 103297 RMVar_ID_103297 Human_SNP_ID_439188452 m1A Human chr10 + 79581120 79581120 79581120 AAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGAAAGAAGAAAGAGAAAAAGAGAGGAAGGGAAAG AAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGGAAGAAGAAAGAGAAAAAGAGAGGAAGGGAAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79581116..79581249 26863196 MeRIP-seq:(Medium) rs535659759 Functional Loss SNV dbSNP153 33..33 33 - - - 103298 RMVar_ID_103298 Human_SNP_ID_439244580 m1A Human chr10 - 79814707 79814707 79814707 TTTTGTTTTTCTGTTGCCTTTAGCAAAACCATATTCCTGCTGCTGTCAGTTATGATGCACTGAGA TTTTGTTTTTCTGTTGCCTTTAGCAAAACCATGTTCCTGCTGCTGTCAGTTATGATGCACTGAGA T C NUTM2B-AS1 Ensembl:ENSG00000225484 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:79814705..79814831 26863196 MeRIP-seq:(Medium) rs1234712493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863109,Human_RBP_ID_1450698,Human_RBP_ID_4137416,Human_RBP_ID_17461206,Human_RBP_ID_17783592 Human_Splice_Rec_1155170,Human_Splice_Rec_1155171,Human_Splice_Rec_1155182,Human_Splice_Rec_1155183,Human_Splice_Rec_1155194,Human_Splice_Rec_1155195,Human_Splice_Rec_1155206,Human_Splice_Rec_1155207,Human_Splice_Rec_1155216,Human_Splice_Rec_1155217,Human_Splice_Rec_1155232,Human_Splice_Rec_1155233,Human_Splice_Rec_1155246,Human_Splice_Rec_1155247,Human_Splice_Rec_1155256,Human_Splice_Rec_1155257,Human_Splice_Rec_1155264,Human_Splice_Rec_1155265,Human_Splice_Rec_1155274,Human_Splice_Rec_1155275,Human_Splice_Rec_1155282,Human_Splice_Rec_1155283,Human_Splice_Rec_1155290,Human_Splice_Rec_1155291,Human_Splice_Rec_1155302,Human_Splice_Rec_1155303,Human_Splice_Rec_1155312,Human_Splice_Rec_1155313,Human_Splice_Rec_1155323,Human_Splice_Rec_1155326,Human_Splice_Rec_1155327 Human_miRNA_ID_3156416,Human_miRNA_ID_3159474,Human_miRNA_ID_3193299,Human_miRNA_ID_3211380 RMVar_hsa_circ_319060,RMVar_hsa_circ_335238 103299 RMVar_ID_103299 Human_SNP_ID_439248064 m1A Human chr10 + 79826351 79826349 79826352 GGCCGGACGCGCTGCGCGGACGGGACGGGGCGAAGGAGGCCGGCAGGCGGAGGAGGAAGCGGCGG GGCCGGACGCGCTGCGCGGACGGGACGGGGC___GGAGGCCGGCAGGCGGAGGAGGAAGCGGCGG CGAA C AL135925.1 Ensembl:ENSG00000272447 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:79826255..79826455 26863196 MeRIP-seq:(Medium) rs1283707370 Functional Loss DEL dbSNP153 32..34 33 - - - 103300 RMVar_ID_103300 Human_SNP_ID_439248064 m1A Human chr10 + 79826352 79826349 79826352 GCCGGACGCGCTGCGCGGACGGGACGGGGCGAAGGAGGCCGGCAGGCGGAGGAGGAAGCGGCGGG GCCGGACGCGCTGCGCGGACGGGACGGGGC___GGAGGCCGGCAGGCGGAGGAGGAAGCGGCGGG CGAA C AL135925.1 Ensembl:ENSG00000272447 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:79826268..79826466 26863196 MeRIP-seq:(Medium) rs1283707370 Functional Loss DEL dbSNP153 31..33 33 - - - 103301 RMVar_ID_103301 Human_SNP_ID_439248066 m1A Human chr10 + 79826355 79826355 79826355 GGACGCGCTGCGCGGACGGGACGGGGCGAAGGAGGCCGGCAGGCGGAGGAGGAAGCGGCGGGGCG GGACGCGCTGCGCGGACGGGACGGGGCGAAGGGGGCCGGCAGGCGGAGGAGGAAGCGGCGGGGCG A G AL135925.1 Ensembl:ENSG00000272447 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:79826241..79826411 26863196 MeRIP-seq:(Medium) rs1485630666 Functional Loss SNV dbSNP153 33..33 33 - - - 103302 RMVar_ID_103302 Human_SNP_ID_439248075 m1A Human chr10 + 79826372 79826372 79826372 GGGACGGGGCGAAGGAGGCCGGCAGGCGGAGGAGGAAGCGGCGGGGCGGCGGCGGCGGCGGCGGC GGGACGGGGCGAAGGAGGCCGGCAGGCGGAGGGGGAAGCGGCGGGGCGGCGGCGGCGGCGGCGGC A G AL135925.1 Ensembl:ENSG00000272447 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr10:79826297..79826384;chr10:79826290..79826404 26863410 MeRIP-seq:(Medium) rs1177016182 Functional Loss SNV dbSNP153 33..33 33 - - - 103303 RMVar_ID_103303 Human_SNP_ID_439253209 m1A Human chr10 + 79848571 79848571 79848571 AAGGCCCAGACTGCCTGCCTGCCACCACCCAGACCCCAGAGGCCAGTGACCAAGGCCCGCCGGCC AAGGCCCAGACTGCCTGCCTGCCACCACCCAGGCCCCAGAGGCCAGTGACCAAGGCCCGCCGGCC A G NUTM2E Ensembl:ENSG00000228570 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79848521..79848607 26863196 MeRIP-seq:(Medium) rs382514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1155378,Human_Splice_Rec_1155388 103304 RMVar_ID_103304 Human_SNP_ID_439325436 m1A Human chr10 + 80141151 80141147 80141151 CTACTGAAATATCTCCTTTCATTTTCTTCCTCACTATTCCTACAGCTCCTGCCTCTGCTCATCAC CTACTGAAATATCTCCTTTCATTTTCTTC____CTATTCCTACAGCTCCTGCCTCTGCTCATCAC CCTCA C PLAC9 Ensembl:ENSG00000189129 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:80141105..80141202 26863196 MeRIP-seq:(Medium) rs1480926857 Functional Loss DEL dbSNP153 30..33 33 - - - 103305 RMVar_ID_103305 Human_SNP_ID_439332406 m1A Human chr10 - 80166949 80166949 80166949 CGGATGAGCAGGCCATCATTGACTGCCTGGGGAGTCGCTCCAACAAGCAGCGGCAGCAGATCCTA CGGATGAGCAGGCCATCATTGACTGCCTGGGGGGTCGCTCCAACAAGCAGCGGCAGCAGATCCTA T C ANXA11 Ensembl:ENSG00000122359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr10:80166900..80167021;chr10:80166901..80166975 26863196,32194978 MeRIP-seq:(Medium) rs1455029856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225796,Human_RBP_ID_383585,Human_RBP_ID_3937917,Human_RBP_ID_8763621,Human_RBP_ID_18187967,Human_RBP_ID_26802784 Human_Splice_Rec_1155604,Human_Splice_Rec_1155630,Human_Splice_Rec_1155660,Human_Splice_Rec_1155686,Human_Splice_Rec_1155718 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_60734,RMVar_hsa_circ_44969,RMVar_hsa_circ_36039 103306 RMVar_ID_103306 Human_SNP_ID_439333028 m1A Human chr10 + 80169068 80169044 80169068 TGCTGCTGCCCAGGGAGTGGCACTGGAGGCTGACCAGGGTAGGTCACTGGTGGCTGCCCAGGGTA TGCTGCTGC________________________CCAGGGTAGGTCACTGGTGGCTGCCCAGGGTA CCCAGGGAGTGGCACTGGAGGCTGA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:80169018..80169375 26863196 MeRIP-seq:(Medium) rs768324733 Functional Loss DEL dbSNP153 10..33 33 - - - 103307 RMVar_ID_103307 Human_SNP_ID_439333041 m1A Human chr10 + 80169068 80169068 80169068 TGCTGCTGCCCAGGGAGTGGCACTGGAGGCTGACCAGGGTAGGTCACTGGTGGCTGCCCAGGGTA TGCTGCTGCCCAGGGAGTGGCACTGGAGGCTGCCCAGGGTAGGTCACTGGTGGCTGCCCAGGGTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:80169018..80169375 26863196 MeRIP-seq:(Medium) rs1564610065 Functional Loss SNV dbSNP153 33..33 33 - - - 103308 RMVar_ID_103308 Human_SNP_ID_439333095 m1A Human chr10 - 80169158 80169158 80169158 CCCTCCAGGATGCCCTCATATCCGCCATACCCAGGGGCCCCTGTGCCGGGCCAGCCCATGCCACC CCCTCCAGGATGCCCTCATATCCGCCATACCCGGGGGCCCCTGTGCCGGGCCAGCCCATGCCACC T C ANXA11 Ensembl:ENSG00000122359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr10:80168949..80169242;chr10:80169051..80169292 26863196 MeRIP-seq:(Medium) rs759288711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4129887,Human_RBP_ID_18187969,Human_RBP_ID_26883017 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_60734,RMVar_hsa_circ_44969,RMVar_hsa_circ_36039 103309 RMVar_ID_103309 Human_SNP_ID_439333096 m1A Human chr10 - 80169158 80169158 80169158 CCCTCCAGGATGCCCTCATATCCGCCATACCCAGGGGCCCCTGTGCCGGGCCAGCCCATGCCACC CCCTCCAGGATGCCCTCATATCCGCCATACCCCGGGGCCCCTGTGCCGGGCCAGCCCATGCCACC T G ANXA11 Ensembl:ENSG00000122359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr10:80168949..80169242;chr10:80169051..80169292 26863196 MeRIP-seq:(Medium) rs759288711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4129887,Human_RBP_ID_18187969,Human_RBP_ID_26883017 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_60734,RMVar_hsa_circ_44969,RMVar_hsa_circ_36039 103310 RMVar_ID_103310 Human_SNP_ID_439333352 m1A Human chr10 + 80169942 80169942 80169942 CCTCACACCCCTTGGCACCTCAGGGCACCGGCATTCCCTAGACATCCATACAGCACTTCCTTCCC CCTCACACCCCTTGGCACCTCAGGGCACCGGCGTTCCCTAGACATCCATACAGCACTTCCTTCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:80169936..80170020 26863196 MeRIP-seq:(Medium) rs1002154716 Functional Loss SNV dbSNP153 33..33 33 - - - 103311 RMVar_ID_103311 Human_SNP_ID_439334126 m1A Human chr10 - 80172864 80172863 80172864 TGAATGTGCTTTCGTCTTCTCTTCCAGATCTAACCATGAGCTACCCTGGCTATCCCCCGCCCCCA TGAATGTGCTTTCGTCTTCTCTTCCAGATCTA_CCATGAGCTACCCTGGCTATCCCCCGCCCCCA GT G ANXA11 Ensembl:ENSG00000122359 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:80172851..80172875 26863196 MeRIP-seq:(Medium) rs1564613951 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4129907,Human_RBP_ID_26883020 Human_Splice_Rec_1155596,Human_Splice_Rec_1155597,Human_Splice_Rec_1155622,Human_Splice_Rec_1155623,Human_Splice_Rec_1155652,Human_Splice_Rec_1155653,Human_Splice_Rec_1155677,Human_Splice_Rec_1155719,Human_Splice_Rec_1155728 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_60734,RMVar_hsa_circ_68489,RMVar_hsa_circ_36039,RMVar_hsa_circ_331272,RMVar_hsa_circ_144602,RMVar_hsa_circ_317697 103312 RMVar_ID_103312 Human_SNP_ID_439334128 m1A Human chr10 - 80172869 80172869 80172869 GAGCCTGAATGTGCTTTCGTCTTCTCTTCCAGATCTAACCATGAGCTACCCTGGCTATCCCCCGC GAGCCTGAATGTGCTTTCGTCTTCTCTTCCAGGTCTAACCATGAGCTACCCTGGCTATCCCCCGC T C ANXA11 Ensembl:ENSG00000122359 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:80172826..80172875 26863196 MeRIP-seq:(Medium) rs766011052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136392 Human_Splice_Rec_1155596,Human_Splice_Rec_1155597,Human_Splice_Rec_1155622,Human_Splice_Rec_1155623,Human_Splice_Rec_1155652,Human_Splice_Rec_1155653,Human_Splice_Rec_1155677,Human_Splice_Rec_1155719,Human_Splice_Rec_1155728 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_60734,RMVar_hsa_circ_68489,RMVar_hsa_circ_36039,RMVar_hsa_circ_331272,RMVar_hsa_circ_144602,RMVar_hsa_circ_317697 103313 RMVar_ID_103313 Human_SNP_ID_439334129 m1A Human chr10 - 80172871 80172871 80172871 CAGAGCCTGAATGTGCTTTCGTCTTCTCTTCCAGATCTAACCATGAGCTACCCTGGCTATCCCCC CAGAGCCTGAATGTGCTTTCGTCTTCTCTTCCGGATCTAACCATGAGCTACCCTGGCTATCCCCC T C ANXA11 Ensembl:ENSG00000122359 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:80172826..80172875 26863196 MeRIP-seq:(Medium) rs750977204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1155597,Human_Splice_Rec_1155623,Human_Splice_Rec_1155653,Human_Splice_Rec_1155677,Human_Splice_Rec_1155719 RMVar_hsa_circ_764,RMVar_hsa_circ_33481,RMVar_hsa_circ_36039,RMVar_hsa_circ_331272,RMVar_hsa_circ_144602,RMVar_hsa_circ_317697 103314 RMVar_ID_103314 Human_SNP_ID_439341855 m1A Human chr10 - 80205394 80205394 80205394 GCGCCGCGCCCGGGACGCCCGCGGAGAGAGCCACTCCCGCCCACGTCCCATTTCGCCCCTCGCGT GCGCCGCGCCCGGGACGCCCGCGGAGAGAGCCCCTCCCGCCCACGTCCCATTTCGCCCCTCGCGT T G ANXA11 Ensembl:ENSG00000122359 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:80205304..80205525 26863196 MeRIP-seq:(Medium) rs1564632371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383594,Human_RBP_ID_748074,Human_RBP_ID_4136394,Human_RBP_ID_5435743,Human_RBP_ID_9274205 Human_Splice_Rec_1155593,Human_Splice_Rec_1155621,Human_Splice_Rec_1155647,Human_Splice_Rec_1155723 RMVar_hsa_circ_15624 103315 RMVar_ID_103315 Human_SNP_ID_439341889 m1A Human chr10 + 80205489 80205489 80205489 CCCGCTCGCGGGGCCCGCGGGGCACTCGGGGCACTGGGGAGCCGCGGGCGCAGCAGCCGTCAGCG CCCGCTCGCGGGGCCCGCGGGGCACTCGGGGCCCTGGGGAGCCGCGGGCGCAGCAGCCGTCAGCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:80205451..80205550 26863196 MeRIP-seq:(Medium) rs937329168 Functional Loss SNV dbSNP153 33..33 33 - - - 103316 RMVar_ID_103316 Human_SNP_ID_439342404 m1A Human chr10 + 80207484 80207484 80207484 AGAAGAGCAGAGGATCAGAGGCACCACCAGAGACTCTCAGAGTGGGTTATTACCCTGGTGGGGGC AGAAGAGCAGAGGATCAGAGGCACCACCAGAGGCTCTCAGAGTGGGTTATTACCCTGGTGGGGGC A G LINC00857 Ensembl:ENSG00000237523 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:80207433..80207561 26863196 MeRIP-seq:(Medium) rs1410413318 Functional Loss SNV dbSNP153 33..33 33 - - - 103317 RMVar_ID_103317 Human_SNP_ID_439342405 m1A Human chr10 + 80207484 80207484 80207484 AGAAGAGCAGAGGATCAGAGGCACCACCAGAGACTCTCAGAGTGGGTTATTACCCTGGTGGGGGC AGAAGAGCAGAGGATCAGAGGCACCACCAGAGTCTCTCAGAGTGGGTTATTACCCTGGTGGGGGC A T LINC00857 Ensembl:ENSG00000237523 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:80207433..80207561 26863196 MeRIP-seq:(Medium) rs1410413318 Functional Loss SNV dbSNP153 33..33 33 - - - 103318 RMVar_ID_103318 Human_SNP_ID_439391260 m1A Human chr10 + 80408637 80408637 80408637 TCGGGGCGGTAAAAGGCCGGCAGAAGGGAGGCACTTGAGGTAGGTGCTGCGCGCCGGGGCTCCGC TCGGGGCGGTAAAAGGCCGGCAGAAGGGAGGCGCTTGAGGTAGGTGCTGCGCGCCGGGGCTCCGC A G PRXL2A Ensembl:ENSG00000122378 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:80408512..80420002 26863196 MeRIP-seq:(Medium) rs1321470535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135916,Human_RBP_ID_5339993,Human_RBP_ID_18416141,Human_RBP_ID_19045541,Human_RBP_ID_22030109 Human_Splice_Rec_1155899,Human_Splice_Rec_1155909,Human_Splice_Rec_1155919 103319 RMVar_ID_103319 Human_SNP_ID_439391268 m1A Human chr10 - 80408665 80408665 80408665 GGCCCCGCCTACGGACATCACGTGCCTCGCGGAGCCCCGGCGCGCAGCACCTACCTCAAGTGCCT GGCCCCGCCTACGGACATCACGTGCCTCGCGGCGCCCCGGCGCGCAGCACCTACCTCAAGTGCCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:80408621..80408751 26863196 MeRIP-seq:(Medium) rs1161574690 Functional Loss SNV dbSNP153 33..33 33 - - - 103320 RMVar_ID_103320 Human_SNP_ID_439402104 m1A Human chr10 - 80454354 80454354 80454354 CCGCGCTCTACTCACCCGCGCGCGGCGGCGGCAGCGGCGGCGCGGCCCGGCTCGGCCGAGGAAGT CCGCGCTCTACTCACCCGCGCGCGGCGGCGGCGGCGGCGGCGCGGCCCGGCTCGGCCGAGGAAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:80454321..80454418;chr10:80454278..80454413 26863196 MeRIP-seq:(Medium) rs1410833488 Functional Loss SNV dbSNP153 33..33 33 - - - 103321 RMVar_ID_103321 Human_SNP_ID_439406981 m1A Human chr10 - 80474235 80474235 80474235 TATCTCTCCTTCCCTCTCATTCTCCGAAGCCAATCCTTCAACACCACCTGGCCTTTGAGGCTCCC TATCTCTCCTTCCCTCTCATTCTCCGAAGCCAGTCCTTCAACACCACCTGGCCTTTGAGGCTCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:80474226..80474384 26863196 MeRIP-seq:(Medium) rs918292409 Functional Loss SNV dbSNP153 33..33 33 - - - 103322 RMVar_ID_103322 Human_SNP_ID_440327558 m1A Human chr10 + 84139588 84139572 84139589 GAAGGGAAACTGCGAGGCGAAGGTGACCGGGGACCGAGGTACTGCTCCGGCTGGCCGGCGGGCGC GAAGGGAAACTGCGAGG_________________CGAGGTACTGCTCCGGCTGGCCGGCGGGCGC GCGAAGGTGACCGGGGAC G GHITM Ensembl:ENSG00000165678 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:84139526..84139845 26863196 MeRIP-seq:(Medium) rs1481839079 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_4136404,Human_RBP_ID_22432536,Human_RBP_ID_23112941,Human_RBP_ID_26775330 Human_Splice_Rec_1156321 103323 RMVar_ID_103323 Human_SNP_ID_440331056 m1A Human chr10 + 84152850 84152850 84152850 GAACTTAGCACTTGTGTTATTGATTAGTGAGGAGCCAGTAAGAAACATCTGGGTATTTGGAAACA GAACTTAGCACTTGTGTTATTGATTAGTGAGGCGCCAGTAAGAAACATCTGGGTATTTGGAAACA A C GHITM Ensembl:ENSG00000165678 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8994215,Human_RBP_ID_17229417,Human_RBP_ID_17787191,Human_RBP_ID_23206499,Human_RBP_ID_24457728,Human_RBP_ID_26399930 Human_miRNA_ID_334596,Human_miRNA_ID_2083359 GWAS_ID_13428,GWAS_ID_13429,GWAS_ID_13430 RMVar_hsa_circ_87092,RMVar_hsa_circ_144651 103324 RMVar_ID_103324 Human_SNP_ID_440829459 m1A Human chr10 + 86117144 86117142 86117145 CCATTACCACAATCAGCAATACTACCACCATCACCACCAACATCACCATCACCAACACCATTACC CCATTACCACAATCAGCAATACTACCACCAT___CACCAACATCACCATCACCAACACCATTACC TCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86117094..86117422 26863196 MeRIP-seq:(Medium) rs1212498529 Functional Loss DEL dbSNP153 32..34 33 - - - 103325 RMVar_ID_103325 Human_SNP_ID_440830596 m1A Human chr10 + 86121516 86121516 86121516 TCATCACCATCATCACCATCACCATCATCATCACTACCATCATCACCATCATCACCATCACCATT TCATCACCATCATCACCATCACCATCATCATCGCTACCATCATCACCATCATCACCATCACCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:86121472..86121598 26863196 MeRIP-seq:(Medium) rs911781037 Functional Loss SNV dbSNP153 33..33 33 - - - 103326 RMVar_ID_103326 Human_SNP_ID_440830603 m1A Human chr10 - 86121523 86121523 86121523 GTGAGATAATGGTGATGGTGATGATGGTGATGATGGTAGTGATGATGATGGTGATGGTGATGATG GTGAGATAATGGTGATGGTGATGATGGTGATGGTGGTAGTGATGATGATGGTGATGGTGATGATG T C GRID1 Ensembl:ENSG00000182771 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86121472..86121579 26863196 MeRIP-seq:(Medium) rs1490548788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2250,RMVar_hsa_circ_332771,RMVar_hsa_circ_144680,RMVar_hsa_circ_107919,RMVar_hsa_circ_144682 103327 RMVar_ID_103327 Human_SNP_ID_440830612 m1A Human chr10 + 86121534 86121532 86121534 TCACCATCATCATCACTACCATCATCACCATCATCACCATCACCATTATCTCACCATCATTATCA TCACCATCATCATCACTACCATCATCACCAT__TCACCATCACCATTATCTCACCATCATTATCA TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:86121484..86121581 26863196 MeRIP-seq:(Medium) rs1447592874 Functional Loss DEL dbSNP153 32..33 33 - - - 103328 RMVar_ID_103328 Human_SNP_ID_440927799 m1A Human chr10 - 86521743 86521743 86521743 TGTTGGAGGAAGGAGGTGGGGGCCGGGAGCGCAAATGGCGTTGAGATGGTTCAGGGCCCTGTTCA TGTTGGAGGAAGGAGGTGGGGGCCGGGAGCGCGAATGGCGTTGAGATGGTTCAGGGCCCTGTTCA T C WAPL Ensembl:ENSG00000062650 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86521398..86521799 26863196 MeRIP-seq:(Medium) rs1163004260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748401,Human_RBP_ID_4130665,Human_RBP_ID_11446334,Human_RBP_ID_22029431 103329 RMVar_ID_103329 Human_SNP_ID_440975508 m1A Human chr10 - 86709293 86709293 86709293 AGTTTTCAAGGGGCCTAGGGTCACCTTTCCCCATGTGTGGCCCAGGGACAATGGGGTCAAAGAGA AGTTTTCAAGGGGCCTAGGGTCACCTTTCCCCTTGTGTGGCCCAGGGACAATGGGGTCAAAGAGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:86709269..86709394 26863196 MeRIP-seq:(Medium) rs919340772 Functional Loss SNV dbSNP153 33..33 33 - - - 103330 RMVar_ID_103330 Human_SNP_ID_440987573 m1A Human chr10 + 86755821 86755821 86755821 CCGCTGGAATTCGCGGGCTCGCAGGTCACAGGAGCCCGGGCGCGCCGGGCCTGGCGCTCCCGAAT CCGCTGGAATTCGCGGGCTCGCAGGTCACAGGGGCCCGGGCGCGCCGGGCCTGGCGCTCCCGAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86755784..86755857 26863196 MeRIP-seq:(Medium) rs1420717622 Functional Loss SNV dbSNP153 33..33 33 - - - 103331 RMVar_ID_103331 Human_SNP_ID_440987754 m1A Human chr10 - 86756297 86756297 86756297 GGCCCGCCGGCCCCTCCCCACAAGCCAGCCCCACAGCTGCCGCCCGGGTAGCTTCCCGCAGACGC GGCCCGCCGGCCCCTCCCCACAAGCCAGCCCCGCAGCTGCCGCCCGGGTAGCTTCCCGCAGACGC T C AC067750.1 Ensembl:ENSG00000272631 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86756250..86756395 26863196 MeRIP-seq:(Medium) rs1021496253 Functional Loss SNV dbSNP153 33..33 33 - - - 103332 RMVar_ID_103332 Human_SNP_ID_440987933 m1A Human chr10 + 86756687 86756687 86756687 TTGGAATCCGCCTGCCGGGCTTGGCGAAGGAGAAGGGAGGAGGCAGGAGCGAGGAGGGAGGAGGG TTGGAATCCGCCTGCCGGGCTTGGCGAAGGAGCAGGGAGGAGGCAGGAGCGAGGAGGGAGGAGGG A C BMPR1A Ensembl:ENSG00000107779 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:86756636..86756713 26863196 MeRIP-seq:(Medium) rs1027922647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135933,Human_RBP_ID_18416300 RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709 103333 RMVar_ID_103333 Human_SNP_ID_440987975 m1A Human chr10 + 86756817 86756817 86756817 CGATCGAGGGGCGACCGGGTCGGGGCCGCTGCACGCCAAGGGCGAAGGCCGATTCGGGCCCCACT CGATCGAGGGGCGACCGGGTCGGGGCCGCTGCCCGCCAAGGGCGAAGGCCGATTCGGGCCCCACT A C BMPR1A Ensembl:ENSG00000107779 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:86756635..86756930 26863196 MeRIP-seq:(Medium) rs1357893294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136408,Human_RBP_ID_9320646 RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709 103334 RMVar_ID_103334 Human_SNP_ID_441040711 m1A Human chr10 + 86958791 86958791 86958791 AGACCAAGCAGGGGGTGACGGAAGCAGCTGAGAAGACCAAGGAGGGGGTCATGTATGTGGGTAAG AGACCAAGCAGGGGGTGACGGAAGCAGCTGAGGAGACCAAGGAGGGGGTCATGTATGTGGGTAAG A G SNCG Ensembl:ENSG00000173267 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:86958611..86959617 26863196 MeRIP-seq:(Medium) rs1340519911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5163072 Human_Splice_Rec_1157477,Human_Splice_Rec_1157485,Human_Splice_Rec_1157491 RMVar_hsa_circ_107626,RMVar_hsa_circ_144726 103335 RMVar_ID_103335 Human_SNP_ID_441040875 m1A Human chr10 - 86959422 86959420 86959422 ATGGGAAGGGGACAGGACAGAATGTGGGGGACAAGAGAGAGCAGGCCTGAGGTAGGGACACTGGC ATGGGAAGGGGACAGGACAGAATGTGGGGGAC__GAGAGAGCAGGCCTGAGGTAGGGACACTGGC CTT C MMRN2 Ensembl:ENSG00000173269 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86959420..86959782 26863196 MeRIP-seq:(Medium) rs974778982 Functional Loss DEL dbSNP153 33..34 33 - - - 103336 RMVar_ID_103336 Human_SNP_ID_441040915 m1A Human chr10 + 86959534 86959534 86959534 CGCCGGCCCCCAGACACCATCCTTACCCCCCCACCGACCCCACAGTTTGTCCAGCTGTTCTGTTG CGCCGGCCCCCAGACACCATCCTTACCCCCCCCCCGACCCCACAGTTTGTCCAGCTGTTCTGTTG A C SNCG Ensembl:ENSG00000173267 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:86959422..86959623 26863196 MeRIP-seq:(Medium) rs1213447655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107626,RMVar_hsa_circ_144726 103337 RMVar_ID_103337 Human_SNP_ID_441041833 m1A Human chr10 + 86962630 86962630 86962630 CTACAGGAGGACTTGAGGCCATCTGCCCCCCAACAGGAGGGTGAGGCATCCAAAGAGAAAGAGGA CTACAGGAGGACTTGAGGCCATCTGCCCCCCAGCAGGAGGGTGAGGCATCCAAAGAGAAAGAGGA A G SNCG Ensembl:ENSG00000173267 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:86962601..86962700 26863196 MeRIP-seq:(Medium) rs1336872469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5137906 Human_Splice_Rec_1157482,Human_Splice_Rec_1157483,Human_Splice_Rec_1157490,Human_Splice_Rec_1157496,Human_Splice_Rec_1157497,Human_Splice_Rec_1157502,Human_Splice_Rec_1157503 RMVar_hsa_circ_107626,RMVar_hsa_circ_144726,RMVar_hsa_circ_88546,RMVar_hsa_circ_144728 103338 RMVar_ID_103338 Human_SNP_ID_441041843 m1A Human chr10 + 86962653 86962653 86962653 TGCCCCCCAACAGGAGGGTGAGGCATCCAAAGAGAAAGAGGAAGTGGCAGAGGAGGTAGGAGCTG TGCCCCCCAACAGGAGGGTGAGGCATCCAAAGGGAAAGAGGAAGTGGCAGAGGAGGTAGGAGCTG A G SNCG Ensembl:ENSG00000173267 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:86962601..86962700 26863196 MeRIP-seq:(Medium) rs758124257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1157482,Human_Splice_Rec_1157483,Human_Splice_Rec_1157490,Human_Splice_Rec_1157496,Human_Splice_Rec_1157497,Human_Splice_Rec_1157502,Human_Splice_Rec_1157503 RMVar_hsa_circ_107626,RMVar_hsa_circ_144726,RMVar_hsa_circ_88546,RMVar_hsa_circ_144728 103339 RMVar_ID_103339 Human_SNP_ID_441044175 m1A Human chr10 + 86970636 86970636 86970636 CCTCCTGAAATGACAGCAGGGAGACTTGGGTGACCCCCCTTCCAGGCGCCATCTAGCACAGCCTG CCTCCTGAAATGACAGCAGGGAGACTTGGGTGGCCCCCCTTCCAGGCGCCATCTAGCACAGCCTG A G ADIRF Ensembl:ENSG00000148671 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:86970587..86970676 26863196 MeRIP-seq:(Medium) rs1564741985 Functional Loss SNV dbSNP153 33..33 33 - - - 103340 RMVar_ID_103340 Human_SNP_ID_441075128 m1A Human chr10 - 87094502 87094502 87094502 GCATCGTGGAGGACAAGCTGGTGGAGGACCTGAGGACCCGGGAGAGCGAGGAGCAGAAGCGGAAC GCATCGTGGAGGACAAGCTGGTGGAGGACCTGGGGACCCGGGAGAGCGAGGAGCAGAAGCGGAAC T C GLUD1 Ensembl:ENSG00000148672 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr10:87094451..87094700;chr10:87094451..87094725 32194978 MeRIP-seq:(Medium) rs1382177904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5488655,Human_RBP_ID_6009243,Human_RBP_ID_22432130 103341 RMVar_ID_103341 Human_SNP_ID_441075129 m1A Human chr10 - 87094502 87094502 87094502 GCATCGTGGAGGACAAGCTGGTGGAGGACCTGAGGACCCGGGAGAGCGAGGAGCAGAAGCGGAAC GCATCGTGGAGGACAAGCTGGTGGAGGACCTGCGGACCCGGGAGAGCGAGGAGCAGAAGCGGAAC T G GLUD1 Ensembl:ENSG00000148672 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr10:87094451..87094700;chr10:87094451..87094725 32194978 MeRIP-seq:(Medium) rs1382177904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5488655,Human_RBP_ID_6009243,Human_RBP_ID_22432130 103342 RMVar_ID_103342 Human_SNP_ID_441075193 m1A Human chr10 - 87094663 87094663 87094663 CTCGGCCGCGTTGCTGGGCTGGGCCCGGGGACAGCCCGCCGCCGCCCCGCAGCCGGGGCTGGCAT CTCGGCCGCGTTGCTGGGCTGGGCCCGGGGACGGCCCGCCGCCGCCCCGCAGCCGGGGCTGGCAT T C GLUD1 Ensembl:ENSG00000148672 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr10:87094568..87094668 26863410 MeRIP-seq:(Medium) rs775436028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_748115,Human_RBP_ID_4130781,Human_RBP_ID_8765684,Human_RBP_ID_22029434,Human_RBP_ID_22431772,Human_RBP_ID_23206707 103343 RMVar_ID_103343 Human_SNP_ID_441075568 m1A Human chr10 - 87095543 87095543 87095543 GGCTGGTGACGCCGAGCCCTCAGCCCGGCCTTACGCGGCGGCGGCTCTGCCTCGCTTTCCTGCCC GGCTGGTGACGCCGAGCCCTCAGCCCGGCCTTCCGCGGCGGCGGCTCTGCCTCGCTTTCCTGCCC T G lnc-GLUD1-1 RNACentral:URS00008B32C3 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:87095535..87095617 26863196 MeRIP-seq:(Medium) rs7896026 Functional Loss SNV dbSNP153 33..33 33 - - - 103344 RMVar_ID_103344 Human_SNP_ID_441080450 m1A Human chr10 + 87116541 87116541 87116541 GTGCAGATGGGGAAGTGTTTGGGTGGCAGGTGAGAATTCGGGATATGAACACTTTATTTTTTTCA GTGCAGATGGGGAAGTGTTTGGGTGGCAGGTGGGAATTCGGGATATGAACACTTTATTTTTTTCA A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87116501..87116683 26863196 MeRIP-seq:(Medium) rs1457846080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805912,Human_RBP_ID_6009303,Human_RBP_ID_11449269,Human_RBP_ID_22885242 RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 103345 RMVar_ID_103345 Human_SNP_ID_441101989 m1A Human chr10 + 87214297 87214297 87214297 CAGCTGCTGGCTCTCTGCAGGGGAGGGAGAGCACCAGTGTGCTCCTGAGCACAGAAGCCCCGTCC CAGCTGCTGGCTCTCTGCAGGGGAGGGAGAGCCCCAGTGTGCTCCTGAGCACAGAAGCCCCGTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:87214247..87214344 26863196 MeRIP-seq:(Medium) rs1242026111 Functional Loss SNV dbSNP153 33..33 33 - - - 103346 RMVar_ID_103346 Human_SNP_ID_441129838 m1A Human chr10 + 87342319 87342319 87342319 CGCTCTGCCTCCTCCTCTTGCTTCATGGAGCCATGCGCCTGGGTGGAGGCTCCCGAGAGAAGCTG CGCTCTGCCTCCTCCTCTTGCTTCATGGAGCCCTGCGCCTGGGTGGAGGCTCCCGAGAGAAGCTG A C LINC00863 Ensembl:ENSG00000224914 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87342273..87342497 26863196 MeRIP-seq:(Medium) rs1243452450 Functional Loss SNV dbSNP153 33..33 33 - - - 103347 RMVar_ID_103347 Human_SNP_ID_441129839 m1A Human chr10 + 87342319 87342319 87342319 CGCTCTGCCTCCTCCTCTTGCTTCATGGAGCCATGCGCCTGGGTGGAGGCTCCCGAGAGAAGCTG CGCTCTGCCTCCTCCTCTTGCTTCATGGAGCCTTGCGCCTGGGTGGAGGCTCCCGAGAGAAGCTG A T LINC00863 Ensembl:ENSG00000224914 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87342273..87342497 26863196 MeRIP-seq:(Medium) rs1243452450 Functional Loss SNV dbSNP153 33..33 33 - - - 103348 RMVar_ID_103348 Human_SNP_ID_441130095 m1A Human chr10 - 87342925 87342925 87342925 CCCCGACCCGGATCCCGAGCTGCGTCGCGGACAATGCCGCGGGCCCGTCCCGGACTACGACTCCC CCCCGACCCGGATCCCGAGCTGCGTCGCGGACGATGCCGCGGGCCCGTCCCGGACTACGACTCCC T C NUTM2A-AS1 RNACentral:URS0000D59868 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:87342890..87342957 26863196 MeRIP-seq:(Medium) rs1045091 Functional Loss SNV dbSNP153 33..33 33 - - - 103349 RMVar_ID_103349 Human_SNP_ID_441163466 m1A Human chr10 - 87504949 87504949 87504949 CGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCGGAGGAGGCAGCCGGGCGCGCGTAGCA CGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGTGGTCCGGAGGAGGCAGCCGGGCGCGCGTAGCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:87504901..87505046 26863196 MeRIP-seq:(Medium) rs747880842 Functional Loss SNV dbSNP153 33..33 33 - - - 103350 RMVar_ID_103350 Human_SNP_ID_441163467 m1A Human chr10 - 87504949 87504949 87504949 CGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCGGAGGAGGCAGCCGGGCGCGCGTAGCA CGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGCGGTCCGGAGGAGGCAGCCGGGCGCGCGTAGCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:87504901..87505046 26863196 MeRIP-seq:(Medium) rs747880842 Functional Loss SNV dbSNP153 33..33 33 - - - 103351 RMVar_ID_103351 Human_SNP_ID_441163489 m1A Human chr10 - 87504975 87504975 87504975 GAGCAGCGCGCAAGCGACGAGAGCAGCGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCG GAGCAGCGCGCAAGCGACGAGAGCAGCGCCGCGGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:87504931..87505054 26863196 MeRIP-seq:(Medium) rs943130812 Functional Loss SNV dbSNP153 33..33 33 - - - 103352 RMVar_ID_103352 Human_SNP_ID_441163490 m1A Human chr10 - 87504975 87504975 87504975 GAGCAGCGCGCAAGCGACGAGAGCAGCGCCGCAGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCG GAGCAGCGCGCAAGCGACGAGAGCAGCGCCGCCGCCAGGGCCGCGGCAGGCGCTACGGAGGTCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:87504931..87505054 26863196 MeRIP-seq:(Medium) rs943130812 Functional Loss SNV dbSNP153 33..33 33 - - - 103353 RMVar_ID_103353 Human_SNP_ID_441163514 m1A Human chr10 - 87505003 87505003 87505003 GGCCACCGGGTCCCTCGGCTCTAGAAGAGAGCAGCGCGCAAGCGACGAGAGCAGCGCCGCAGCCA GGCCACCGGGTCCCTCGGCTCTAGAAGAGAGCTGCGCGCAAGCGACGAGAGCAGCGCCGCAGCCA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:87504901..87505150 26863410 MeRIP-seq:(Medium) rs766943784 Functional Loss SNV dbSNP153 33..33 33 - - - 103354 RMVar_ID_103354 Human_SNP_ID_441212379 m1A Human chr10 + 87713188 87713188 87713188 TGGATGGGGACAATGTCCGTCATGGCCTTAACAGAAATCTCGGATTCTCTCCTGGGGACAGAGAG TGGATGGGGACAATGTCCGTCATGGCCTTAACCGAAATCTCGGATTCTCTCCTGGGGACAGAGAG A C PAPSS2 Ensembl:ENSG00000198682 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:87713138..87714071 32194978 MeRIP-seq:(Medium) rs1180753301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_384289,Human_RBP_ID_4130997 Human_miRNA_ID_424868,Human_miRNA_ID_2136651,Human_miRNA_ID_2665445 RMVar_hsa_circ_68976,RMVar_hsa_circ_274995,RMVar_hsa_circ_360680,RMVar_hsa_circ_289211,RMVar_hsa_circ_72048,RMVar_hsa_circ_144756 103355 RMVar_ID_103355 Human_SNP_ID_441236035 m1A Human chr10 + 87814506 87814506 87814506 ATCAATTGCATCTACCATCCATTTGATAGTAAAGTATGTCACTGCACCAAATATTGTCAAACGGA ATCAATTGCATCTACCATCCATTTGATAGTAACGTATGTCACTGCACCAAATATTGTCAAACGGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:87792729..87814610 32194978 MeRIP-seq:(Medium) rs1488159734 Functional Loss SNV dbSNP153 33..33 33 - - - 103356 RMVar_ID_103356 Human_SNP_ID_441236897 m1A Human chr10 - 87818084 87818084 87818084 TGAGGTCCTTTAAGGACCGTCTCGGACCTGGGAACCCCCGGAGGAAAGGTCACCCCGGTCTTCTC TGAGGTCCTTTAAGGACCGTCTCGGACCTGGGGACCCCCGGAGGAAAGGTCACCCCGGTCTTCTC T C ATAD1 Ensembl:ENSG00000138138 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:87818064..87818163 26863196 MeRIP-seq:(Medium) rs1173205987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136910,Human_RBP_ID_6010560,Human_RBP_ID_18416144 103357 RMVar_ID_103357 Human_SNP_ID_441236903 m1A Human chr10 + 87818108 87818108 87818108 CCGGGGGTTCCCAGGTCCGAGACGGTCCTTAAAGGACCTCAGAAGGATACGACAACCATCCCATG CCGGGGGTTCCCAGGTCCGAGACGGTCCTTAAGGGACCTCAGAAGGATACGACAACCATCCCATG A G CFL1P1 Ensembl:ENSG00000223820 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87818057..87818157 26863196 MeRIP-seq:(Medium) rs1241322777 Functional Loss SNV dbSNP153 33..33 33 - - - 103358 RMVar_ID_103358 Human_SNP_ID_441247719 m1A Human chr10 + 87863809 87863797 87863809 CCTCGGGGAGCCGGCCGGCCTGCGGCGGCGGCAGCGGCGGCGTTTCTCGCCTCCTCTTCGTCTTT CCTCGGGGAGCCGGCCGGCCT____________GCGGCGGCGTTTCTCGCCTCCTCTTCGTCTTT TGCGGCGGCGGCA T PTEN Ensembl:ENSG00000171862 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:87863626..87864024 26863196 MeRIP-seq:(Medium) rs786204880 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_225954,Human_RBP_ID_4136912,Human_RBP_ID_22156614 Clinvar_Rec_641 103359 RMVar_ID_103359 Human_SNP_ID_441247830 m1A Human chr10 - 87863994 87863982 87863994 ACAGGCGACTCAGACCCCCTCCCTGGAGCTGCAGCCGCCGCGGCCGCCGCCGCCGCCGCTTCTCC ACAGGCGACTCAGACCCCCTCCCTGGAGCTGC____________CGCCGCCGCCGCCGCTTCTCC GGCCGCGGCGGCT G lnc-KLLN-2,lnc-KLLN-2:2 RNACentral:URS00008C2367,RNACentral:URS00008C4038 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:87863976..87864000 26863196 MeRIP-seq:(Medium) rs1329229030 Functional Loss DEL dbSNP153 33..44 33 - - - 103360 RMVar_ID_103360 Human_SNP_ID_441247834 m1A Human chr10 - 87863994 87863985 87863994 ACAGGCGACTCAGACCCCCTCCCTGGAGCTGCAGCCGCCGCGGCCGCCGCCGCCGCCGCTTCTCC ACAGGCGACTCAGACCCCCTCCCTGGAGCTGC_________GGCCGCCGCCGCCGCCGCTTCTCC CGCGGCGGCT C lnc-KLLN-2,lnc-KLLN-2:2 RNACentral:URS00008C2367,RNACentral:URS00008C4038 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:87863976..87864000 26863196 MeRIP-seq:(Medium) rs1226857287 Functional Loss DEL dbSNP153 33..41 33 - - - Clinvar_Rec_642 103361 RMVar_ID_103361 Human_SNP_ID_441248000 m1A Human chr10 + 87864349 87864349 87864349 TACCCGGCTGCGGTCCAGAGCCAAGCGGCGGCAGAGCGAGGGGCATCAGCTACCGCCAAGTCCAG TACCCGGCTGCGGTCCAGAGCCAAGCGGCGGCGGAGCGAGGGGCATCAGCTACCGCCAAGTCCAG A G PTEN Ensembl:ENSG00000171862 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:87864226..87864450 26863196 MeRIP-seq:(Medium) rs886047395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_107504,Human_RBP_ID_8725037,Human_RBP_ID_22029442 Clinvar_Rec_643 103362 RMVar_ID_103362 Human_SNP_ID_441260649 m1A Human chr10 - 87914750 87914750 87914750 TTTTCAGTTTCTAAGGAAAGACTTGAATGGTAAATCAGTTAGTTTGAGTCAATTTCAGCTCTTTG TTTTCAGTTTCTAAGGAAAGACTTGAATGGTATATCAGTTAGTTTGAGTCAATTTCAGCTCTTTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:87914660..87914825 26863196 MeRIP-seq:(Medium) rs958250154 Functional Loss SNV dbSNP153 33..33 33 - - - 103363 RMVar_ID_103363 Human_SNP_ID_441266432 m1A Human chr10 + 87938688 87938688 87938688 GTGGTGGGTACAAGTTGACCATAAAATAACGCATTAGGTTAGTAATGCCCAAATAATACTTTGGG GTGGTGGGTACAAGTTGACCATAAAATAACGCGTTAGGTTAGTAATGCCCAAATAATACTTTGGG A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87938650..87938762 26863196 MeRIP-seq:(Medium) rs564469381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79848,RMVar_hsa_circ_281325,RMVar_hsa_circ_283760,RMVar_hsa_circ_328578,RMVar_hsa_circ_144782,RMVar_hsa_circ_76492,RMVar_hsa_circ_144781 103364 RMVar_ID_103364 Human_SNP_ID_441268431 m1A Human chr10 - 87946888 87946888 87946888 ACTTTGTTCTCCCAACCTCTCTCTTGATCCTGACCAACACATCACCTTCGATGAATTCAGCTCCT ACTTTGTTCTCCCAACCTCTCTCTTGATCCTGGCCAACACATCACCTTCGATGAATTCAGCTCCT T C lnc-KLLN-1 RNACentral:URS00008BF54B lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:87946838..87947031 26863196 MeRIP-seq:(Medium) rs1324393758 Functional Loss SNV dbSNP153 33..33 33 - - - 103365 RMVar_ID_103365 Human_SNP_ID_441270620 m1A Human chr10 - 87954914 87954914 87954914 CTTCTTCTTCCTAAACCCAAGTTGCCATTCTTATCTCAGTCCTCACCCTCTCCTTTTCTTCCTTT CTTCTTCTTCCTAAACCCAAGTTGCCATTCTTTTCTCAGTCCTCACCCTCTCCTTTTCTTCCTTT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:87954797..87954948 26863196 MeRIP-seq:(Medium) rs1040171131 Functional Loss SNV dbSNP153 33..33 33 - - - 103366 RMVar_ID_103366 Human_SNP_ID_441482381 m1A Human chr10 - 88880426 88880426 88880426 CGGCCGTGCCTCCTCCCCCTTCTCCTCTGCCGACAGATGGAGCTTTGCTGGTTCCAGTCGCGCGG CGGCCGTGCCTCCTCCCCCTTCTCCTCTGCCGGCAGATGGAGCTTTGCTGGTTCCAGTCGCGCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:88880278..88880436 26863196 MeRIP-seq:(Medium) rs1335092781 Functional Loss SNV dbSNP153 33..33 33 - - - 103367 RMVar_ID_103367 Human_SNP_ID_441498999 m1A Human chr10 + 88952669 88952669 88952669 CAGCCAAATCCCTGCAGATGATGTCTTATTATACCGGGTAATTAAAAGAGCCACTGGAATCTATA CAGCCAAATCCCTGCAGATGATGTCTTATTATGCCGGGTAATTAAAAGAGCCACTGGAATCTATA A G STAMBPL1 Ensembl:ENSG00000138134 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:88952664..88952748 26863196 MeRIP-seq:(Medium) rs894969584 Functional Loss SNV dbSNP153 33..33 33 - - - 103368 RMVar_ID_103368 Human_SNP_ID_441561258 m1A Human chr10 - 89214997 89214997 89214997 GCTTGTGCCGACTGCAGTCTGGAGCGGGGGTCACGACTGGCTTGCAGATGTCTACGACGTCAATA GCTTGTGCCGACTGCAGTCTGGAGCGGGGGTCGCGACTGGCTTGCAGATGTCTACGACGTCAATA T C LIPA Ensembl:ENSG00000107798 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:89214956..89215982 32194978 MeRIP-seq:(Medium) rs758500611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_384663,Human_RBP_ID_8994735,Human_RBP_ID_22431783,Human_RBP_ID_22752887,Human_RBP_ID_23475550 Human_Splice_Rec_1158864,Human_Splice_Rec_1158882,Human_Splice_Rec_1158896 RMVar_hsa_circ_144797,RMVar_hsa_circ_85581 103369 RMVar_ID_103369 Human_SNP_ID_441570037 m1A Human chr10 + 89251786 89251786 89251786 GGCCGCTGTCTCGAGTCGCAGTGCCAGCTCTCAGGGGCCGGGGTGCGGATAGGGGACCTGCAGGG GGCCGCTGTCTCGAGTCGCAGTGCCAGCTCTCGGGGGCCGGGGTGCGGATAGGGGACCTGCAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:89251690..89251820 26863196 MeRIP-seq:(Medium) rs915845755 Functional Loss SNV dbSNP153 33..33 33 - - - 103370 RMVar_ID_103370 Human_SNP_ID_441605273 m1A Human chr10 - 89402628 89402628 89402628 AAAGCTTCTTGCAAATGTTCTCCACCTTGTCCAGGTAAGTCTGGGCTTCTGCCAGTCTGCCCATG AAAGCTTCTTGCAAATGTTCTCCACCTTGTCCGGGTAAGTCTGGGCTTCTGCCAGTCTGCCCATG T C LIPA Ensembl:ENSG00000107798 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:89402558..89402693 32194978 MeRIP-seq:(Medium) rs765564669 Functional Loss SNV dbSNP153 33..33 33 - - - 103371 RMVar_ID_103371 Human_SNP_ID_441662980 m1A Human chr10 - 89645188 89645188 89645188 CGTTTGAAGTCGCGCGGCCTGGGGATCAGGGGAAGGCGGGCGGCGGGAGCCCCGGCTGGGGGTGC CGTTTGAAGTCGCGCGGCCTGGGGATCAGGGGGAGGCGGGCGGCGGGAGCCCCGGCTGGGGGTGC T C PANK1,AL157400.5 Ensembl:ENSG00000152782,Ensembl:ENSG00000249962 Protein coding,Pseudogene CDS,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:89645087..89645200 26863196 MeRIP-seq:(Medium) rs759155595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805189,Human_RBP_ID_3364060,Human_RBP_ID_4135946,Human_RBP_ID_5164715,Human_RBP_ID_5488686,Human_RBP_ID_8172269,Human_RBP_ID_8244785,Human_RBP_ID_8765891,Human_RBP_ID_9413756,Human_RBP_ID_11485520,Human_RBP_ID_17108072,Human_RBP_ID_17462310,Human_RBP_ID_18416147,Human_RBP_ID_18468853,Human_RBP_ID_21915818,Human_RBP_ID_21959465,Human_RBP_ID_21964966 103372 RMVar_ID_103372 Human_SNP_ID_441741153 m1A Human chr10 + 89978717 89978717 89978717 AACGGGAATGAACCGAGAGCGTAGTGACCATCATGAGCCTCCTTAACAAGTCCAAGAGTGAGATG AACGGGAATGAACCGAGAGCGTAGTGACCATCGTGAGCCTCCTTAACAAGTCCAAGAGTGAGATG A G SNRPD2P1,LINC01374 Ensembl:ENSG00000228938,Ensembl:ENSG00000280560 Pseudogene,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:89978693..89978810 26863196 MeRIP-seq:(Medium) rs1206548924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_984892,Human_RBP_ID_1353044,Human_RBP_ID_1451437,Human_RBP_ID_3360413,Human_RBP_ID_4144395,Human_RBP_ID_8341314,Human_RBP_ID_17788211,Human_RBP_ID_18600010,Human_RBP_ID_22490469,Human_RBP_ID_26399957,Human_RBP_ID_26600787,Human_RBP_ID_26883513,Human_RBP_ID_27407715 103373 RMVar_ID_103373 Human_SNP_ID_74306325 m1A Human chr2 + 60418867 60418864 60418867 GCAAGAACCCCCCACCCCTTCTCTGTGTCTCTACTTTTTTCTGGGCTTGCCTCCTTCACTATGGG GCAAGAACCCCCCACCCCTTCTCTGTGTCT___CTTTTTTCTGGGCTTGCCTCCTTCACTATGGG TCTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:60418851..60418951;chr2:60418851..60418935 26863196 MeRIP-seq:(Medium) rs1335417471 Functional Loss DEL dbSNP153 31..33 33 - - - 103374 RMVar_ID_103374 Human_SNP_ID_74306326 m1A Human chr2 + 60418867 60418867 60418867 GCAAGAACCCCCCACCCCTTCTCTGTGTCTCTACTTTTTTCTGGGCTTGCCTCCTTCACTATGGG GCAAGAACCCCCCACCCCTTCTCTGTGTCTCTCCTTTTTTCTGGGCTTGCCTCCTTCACTATGGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:60418851..60418951;chr2:60418851..60418935 26863196 MeRIP-seq:(Medium) rs1028586108 Functional Loss SNV dbSNP153 33..33 33 - - - 103375 RMVar_ID_103375 Human_SNP_ID_74401293 m1A Human chr2 - 60756348 60756348 60756348 AGCTCGCTTGCTCGCTCACTTTCCCACTTACTATGGCTGAGGCATCCAACCGAGTAGTGAAAACA AGCTCGCTTGCTCGCTCACTTTCCCACTTACTGTGGCTGAGGCATCCAACCGAGTAGTGAAAACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:60756297..60756431;chr2:60756297..60756457 26863196 MeRIP-seq:(Medium) rs1253036623 Functional Loss SNV dbSNP153 33..33 33 - - - 103376 RMVar_ID_103376 Human_SNP_ID_74483382 m1A Human chr2 + 61068796 61068796 61068796 TAGTCCTCACTCTTTGCCAGGTAGCACTTTCCATATATCCTCAGAAGTATGTAAGCTAGCTACTA TAGTCCTCACTCTTTGCCAGGTAGCACTTTCCGTATATCCTCAGAAGTATGTAAGCTAGCTACTA A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61068794..61068916 26863196 MeRIP-seq:(Medium) rs1019249176 Functional Loss SNV dbSNP153 33..33 33 - - - 103377 RMVar_ID_103377 Human_SNP_ID_74491775 m1A Human chr2 - 61099087 61099087 61099087 GCCTCAGGCTCTTTCAGTCTCTTTTACTCACTATGTTCCTTCTGACCTTGCTGTTCTGACTAGAA GCCTCAGGCTCTTTCAGTCTCTTTTACTCACTGTGTTCCTTCTGACCTTGCTGTTCTGACTAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61098977..61099109 26863196 MeRIP-seq:(Medium) rs1553433685 Functional Loss SNV dbSNP153 33..33 33 - - - 103378 RMVar_ID_103378 Human_SNP_ID_74502341 m1A Human chr2 - 61138998 61138994 61138998 ACGAAGGAAGGAAGGAAGGAGAGAAGGAAGGAAGGAGGGAGAGAAAGAGAAAGAAAAAGGAAGGA ACGAAGGAAGGAAGGAAGGAGAGAAGGAAGGA____GGGAGAGAAAGAGAAAGAAAAAGGAAGGA CTCCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61138931..61139035 26863196 MeRIP-seq:(Medium) rs760353593 Functional Loss DEL dbSNP153 33..36 33 - - - 103379 RMVar_ID_103379 Human_SNP_ID_74514903 m1A Human chr2 - 61181506 61181506 61181506 AGGCCCTCCACAAGGCACCCGAACTACCACACAGGAACCACACAGTCTGATCAACACTATTTGAA AGGCCCTCCACAAGGCACCCGAACTACCACACTGGAACCACACAGTCTGATCAACACTATTTGAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:61181500..61181609 26863196 MeRIP-seq:(Medium) rs575141789 Functional Loss SNV dbSNP153 33..33 33 - - - 103380 RMVar_ID_103380 Human_SNP_ID_74514910 m1A Human chr2 - 61181522 61181522 61181522 ATCCTTCTCGGCAAACAGGCCCTCCACAAGGCACCCGAACTACCACACAGGAACCACACAGTCTG ATCCTTCTCGGCAAACAGGCCCTCCACAAGGCGCCCGAACTACCACACAGGAACCACACAGTCTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:61181517..61181612 26863196 MeRIP-seq:(Medium) rs560183192 Functional Loss SNV dbSNP153 33..33 33 - - - 103381 RMVar_ID_103381 Human_SNP_ID_74525214 m1A Human chr2 - 61214151 61214151 61214151 GTACTATGGCATTCTGAGGCTCTGCTGTGAGCAGTCTCCTGCATTCACACGACAACTGGCTTCTC GTACTATGGCATTCTGAGGCTCTGCTGTGAGCTGTCTCCTGCATTCACACGACAACTGGCTTCTC T A USP34 Ensembl:ENSG00000115464 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:61214102..61214181 32194978 MeRIP-seq:(Medium) rs778399958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57408,Human_RBP_ID_9297261,Human_RBP_ID_13926556,Human_RBP_ID_22077079 Human_Splice_Rec_251041,Human_Splice_Rec_251195,Human_Splice_Rec_251304,Human_Splice_Rec_251305,Human_Splice_Rec_251317 Human_miRNA_ID_3085271 RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_14184,RMVar_hsa_circ_50845,RMVar_hsa_circ_85115,RMVar_hsa_circ_99836,RMVar_hsa_circ_77357,RMVar_hsa_circ_92887,RMVar_hsa_circ_200274,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_200275,RMVar_hsa_circ_117308,RMVar_hsa_circ_59337,RMVar_hsa_circ_82566,RMVar_hsa_circ_34286,RMVar_hsa_circ_114329,RMVar_hsa_circ_200279,RMVar_hsa_circ_200280,RMVar_hsa_circ_200281,RMVar_hsa_circ_200278,RMVar_hsa_circ_267606,RMVar_hsa_circ_29974,RMVar_hsa_circ_52114,RMVar_hsa_circ_200282,RMVar_hsa_circ_268313,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_70432,RMVar_hsa_circ_116467,RMVar_hsa_circ_90618,RMVar_hsa_circ_200284,RMVar_hsa_circ_200283,RMVar_hsa_circ_376752,RMVar_hsa_circ_355136,RMVar_hsa_circ_300979,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_38229,RMVar_hsa_circ_47637,RMVar_hsa_circ_200289,RMVar_hsa_circ_200290,RMVar_hsa_circ_200288,RMVar_hsa_circ_291035,RMVar_hsa_circ_327795,RMVar_hsa_circ_124258,RMVar_hsa_circ_32858,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_53203,RMVar_hsa_circ_200296,RMVar_hsa_circ_32190,RMVar_hsa_circ_15730,RMVar_hsa_circ_200297,RMVar_hsa_circ_200294,RMVar_hsa_circ_200295,RMVar_hsa_circ_200293,RMVar_hsa_circ_2015,RMVar_hsa_circ_108164,RMVar_hsa_circ_200301,RMVar_hsa_circ_341635,RMVar_hsa_circ_200291,RMVar_hsa_circ_319868,RMVar_hsa_circ_200302,RMVar_hsa_circ_113788,RMVar_hsa_circ_378275,RMVar_hsa_circ_372869,RMVar_hsa_circ_109227,RMVar_hsa_circ_65093,RMVar_hsa_circ_77073,RMVar_hsa_circ_48860,RMVar_hsa_circ_17507,RMVar_hsa_circ_34855,RMVar_hsa_circ_118083,RMVar_hsa_circ_200304,RMVar_hsa_circ_200306,RMVar_hsa_circ_200307,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_52447,RMVar_hsa_circ_89816,RMVar_hsa_circ_46122,RMVar_hsa_circ_77201,RMVar_hsa_circ_98070,RMVar_hsa_circ_200308,RMVar_hsa_circ_200309,RMVar_hsa_circ_99239,RMVar_hsa_circ_97557,RMVar_hsa_circ_45576,RMVar_hsa_circ_200310,RMVar_hsa_circ_200312,RMVar_hsa_circ_200313,RMVar_hsa_circ_200311 103382 RMVar_ID_103382 Human_SNP_ID_74601283 m1A Human chr2 - 61444778 61444778 61444778 ACGTGCGGTGGACACCTGCCAGGTATATATGCAGAGGCTGGAGGAGGCAATGTCTGATTTGCATA ACGTGCGGTGGACACCTGCCAGGTATATATGCGGAGGCTGGAGGAGGCAATGTCTGATTTGCATA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61444776..61444891 26863196 MeRIP-seq:(Medium) rs1304077401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936295,Human_RBP_ID_13930349 103383 RMVar_ID_103383 Human_SNP_ID_74610644 m1A Human chr2 + 61470667 61470667 61470667 ACCGCGGCTACTTACTTTCATTTAACACCTCCACCAGGTCTGCGCAGTTCTCGCACATCGTTCGG ACCGCGGCTACTTACTTTCATTTAACACCTCCCCCAGGTCTGCGCAGTTCTCGCACATCGTTCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:61420802..61470769 26863196 MeRIP-seq:(Medium) rs765752761 Functional Loss SNV dbSNP153 33..33 33 - - - 103384 RMVar_ID_103384 Human_SNP_ID_74610661 m1A Human chr2 - 61470696 61470696 61470696 TCCGAAGCGGGGGAGGGGGGGGGCGGCGGCCGAACGATGTGCGAGAACTGCGCAGACCTGGTGGA TCCGAAGCGGGGGAGGGGGGGGGCGGCGGCCGCACGATGTGCGAGAACTGCGCAGACCTGGTGGA T G USP34 Ensembl:ENSG00000115464 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:61470607..61470698 26863196 MeRIP-seq:(Medium) rs1375806682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60889,Human_RBP_ID_776822,Human_RBP_ID_2655475,Human_RBP_ID_4612874,Human_RBP_ID_5131586,Human_RBP_ID_5196502,Human_RBP_ID_5322478,Human_RBP_ID_17570394,Human_RBP_ID_17959172,Human_RBP_ID_18949204,Human_RBP_ID_23115028,Human_RBP_ID_24377484,Human_RBP_ID_25555511 Human_Splice_Rec_251061,Human_Splice_Rec_251415 103385 RMVar_ID_103385 Human_SNP_ID_74610985 m1A Human chr2 - 61471194 61471194 61471194 GGCGGGGTGTGGAGCGTGCGGCGTGTGTGCGGAGGGAGAGGTGGGGGGCGGAGGAGAGGCGAGAA GGCGGGGTGTGGAGCGTGCGGCGTGTGTGCGGCGGGAGAGGTGGGGGGCGGAGGAGAGGCGAGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:61470837..61471224 26863196 MeRIP-seq:(Medium) rs1051576306 Functional Loss SNV dbSNP153 33..33 33 - - - 103386 RMVar_ID_103386 Human_SNP_ID_74615257 m1A Human chr2 + 61483036 61483036 61483036 ATATCACAAAAATAAGTTTGATAAAAACTCTGAGCTGCAGCTTCTTCTTGTGCAACATTTTGTAA ATATCACAAAAATAAGTTTGATAAAAACTCTGGGCTGCAGCTTCTTCTTGTGCAACATTTTGTAA A G AC016727.1 Ensembl:ENSG00000270820 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:61482943..61483043 32194978 MeRIP-seq:(Medium) rs752526623 Functional Loss SNV dbSNP153 33..33 33 - - - 103387 RMVar_ID_103387 Human_SNP_ID_74616233 m1A Human chr2 + 61485924 61485924 61485924 GCAGCTGGGACATTTCTCTGATAATCAATGAGAACTGCATCCAACAGAGGGGGAACAAAATTTTC GCAGCTGGGACATTTCTCTGATAATCAATGAGTACTGCATCCAACAGAGGGGGAACAAAATTTTC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:61485901..61485925 26863196 MeRIP-seq:(Medium) rs1376737897 Functional Loss SNV dbSNP153 33..33 33 - - - 103388 RMVar_ID_103388 Human_SNP_ID_74618822 m1A Human chr2 - 61494079 61494079 61494079 AGTTTTGGTCTTCTGTGTAGGCCCTTCATTATATGTTGTTGGTATCTGAAGTAGAAGAAACTGAA AGTTTTGGTCTTCTGTGTAGGCCCTTCATTATGTGTTGTTGGTATCTGAAGTAGAAGAAACTGAA T C XPO1 Ensembl:ENSG00000082898 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:61494029..61494129 32194978 MeRIP-seq:(Medium) rs1447130097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915504,Human_RBP_ID_1921062,Human_RBP_ID_2655630,Human_RBP_ID_10484048,Human_RBP_ID_13931506,Human_RBP_ID_20587123,Human_RBP_ID_22994336,Human_RBP_ID_23878886,Human_RBP_ID_25555811,Human_RBP_ID_27840266 Human_Splice_Rec_251478,Human_Splice_Rec_251526,Human_Splice_Rec_251594,Human_Splice_Rec_251642,Human_Splice_Rec_251686 RMVar_hsa_circ_1574,RMVar_hsa_circ_265025,RMVar_hsa_circ_315608,RMVar_hsa_circ_352064,RMVar_hsa_circ_61674,RMVar_hsa_circ_23408,RMVar_hsa_circ_3630,RMVar_hsa_circ_272166,RMVar_hsa_circ_200502,RMVar_hsa_circ_200503,RMVar_hsa_circ_309105,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_272030,RMVar_hsa_circ_200514,RMVar_hsa_circ_200511,RMVar_hsa_circ_200512,RMVar_hsa_circ_200510,RMVar_hsa_circ_200518,RMVar_hsa_circ_306485,RMVar_hsa_circ_332879,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_292172,RMVar_hsa_circ_200519,RMVar_hsa_circ_81351,RMVar_hsa_circ_200516,RMVar_hsa_circ_200517,RMVar_hsa_circ_200515,RMVar_hsa_circ_73640,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_75681,RMVar_hsa_circ_287634,RMVar_hsa_circ_311324,RMVar_hsa_circ_200525,RMVar_hsa_circ_327523,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_106519,RMVar_hsa_circ_200530,RMVar_hsa_circ_200532,RMVar_hsa_circ_200533,RMVar_hsa_circ_200531,RMVar_hsa_circ_200528,RMVar_hsa_circ_200529,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_323336,RMVar_hsa_circ_321705,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_53456,RMVar_hsa_circ_200540,RMVar_hsa_circ_200539,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_330990,RMVar_hsa_circ_338245,RMVar_hsa_circ_295297,RMVar_hsa_circ_296364,RMVar_hsa_circ_293456,RMVar_hsa_circ_273499,RMVar_hsa_circ_125221,RMVar_hsa_circ_2957,RMVar_hsa_circ_200558,RMVar_hsa_circ_200543,RMVar_hsa_circ_200547,RMVar_hsa_circ_200549,RMVar_hsa_circ_200550,RMVar_hsa_circ_200548,RMVar_hsa_circ_200545,RMVar_hsa_circ_200546,RMVar_hsa_circ_200544,RMVar_hsa_circ_275007,RMVar_hsa_circ_292518,RMVar_hsa_circ_308693,RMVar_hsa_circ_313165,RMVar_hsa_circ_304583,RMVar_hsa_circ_282169,RMVar_hsa_circ_30436,RMVar_hsa_circ_9187,RMVar_hsa_circ_200559,RMVar_hsa_circ_200554,RMVar_hsa_circ_200556,RMVar_hsa_circ_200557,RMVar_hsa_circ_200555,RMVar_hsa_circ_111227,RMVar_hsa_circ_346816,RMVar_hsa_circ_331786,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_10985,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_200562,RMVar_hsa_circ_323126,RMVar_hsa_circ_54917,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_317224,RMVar_hsa_circ_292435,RMVar_hsa_circ_292977,RMVar_hsa_circ_271740,RMVar_hsa_circ_200564,RMVar_hsa_circ_200566,RMVar_hsa_circ_200567,RMVar_hsa_circ_200568,RMVar_hsa_circ_200565,RMVar_hsa_circ_200563 103389 RMVar_ID_103389 Human_SNP_ID_74619681 m1A Human chr2 + 61496951 61496951 61496951 AATTGTTCTTCATATTGGCTTACACTCACACCAGCAATCTCAGTGAGGCACTTCAGAGAGACATT AATTGTTCTTCATATTGGCTTACACTCACACCGGCAATCTCAGTGAGGCACTTCAGAGAGACATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:61496901..61497002 32194978 MeRIP-seq:(Medium) rs763749686 Functional Loss SNV dbSNP153 33..33 33 - - - 103390 RMVar_ID_103390 Human_SNP_ID_74631884 m1A Human chr2 + 61536612 61536612 61536612 TTAGGTTGTGTGGGCAATCGCCCGCTTCATTCAGGAAAAACACACCTCATTAGGGCCCGCCCTCC TTAGGTTGTGTGGGCAATCGCCCGCTTCATTCCGGAAAAACACACCTCATTAGGGCCCGCCCTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:61536600..61536844 26863196 MeRIP-seq:(Medium) rs777452986 Functional Loss SNV dbSNP153 33..33 33 - - - 103391 RMVar_ID_103391 Human_SNP_ID_74631929 m1A Human chr2 + 61536732 61536732 61536732 ACGCACTCACCCCGCCCTTACTCGGAGGAGGCATTTAGACCAGGCGCCTTAAGTTCACCGCCCCT ACGCACTCACCCCGCCCTTACTCGGAGGAGGCTTTTAGACCAGGCGCCTTAAGTTCACCGCCCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:61536728..61536878 26863196 MeRIP-seq:(Medium) rs1558688176 Functional Loss SNV dbSNP153 33..33 33 - - - 103392 RMVar_ID_103392 Human_SNP_ID_74632432 m1A Human chr2 + 61537921 61537921 61537921 CCCAGGGGGACCCTCCAGCCACAGGCAGCAGCAGAAGCGGCAGGAGTAGGGGGTGTAGAGTCCAC CCCAGGGGGACCCTCCAGCCACAGGCAGCAGCGGAAGCGGCAGGAGTAGGGGGTGTAGAGTCCAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:61537776..61537975 26863196 MeRIP-seq:(Medium) rs1432658316 Functional Loss SNV dbSNP153 33..33 33 - - - 103393 RMVar_ID_103393 Human_SNP_ID_74632459 m1A Human chr2 - 61537981 61537981 61537981 GCCGTGTTTTGGTAGGGGGGAGTCGGACTGCAACTGGCAGCAGAGCGTCTCCCCGGCCGTGTGGA GCCGTGTTTTGGTAGGGGGGAGTCGGACTGCAGCTGGCAGCAGAGCGTCTCCCCGGCCGTGTGGA T C XPO1 Ensembl:ENSG00000082898 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:61537892..61538219 26863410 MeRIP-seq:(Medium) rs997031774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242304,Human_RBP_ID_774747,Human_RBP_ID_922151,Human_RBP_ID_1067927,Human_RBP_ID_1301801,Human_RBP_ID_1588643,Human_RBP_ID_3630541,Human_RBP_ID_3959074,Human_RBP_ID_4613076,Human_RBP_ID_5146556,Human_RBP_ID_5322080,Human_RBP_ID_5651504,Human_RBP_ID_6937287,Human_RBP_ID_8110203,Human_RBP_ID_8201485,Human_RBP_ID_8233939,Human_RBP_ID_8942576,Human_RBP_ID_9428670,Human_RBP_ID_13933699,Human_RBP_ID_18421791,Human_RBP_ID_18763507,Human_RBP_ID_18947868,Human_RBP_ID_22075330,Human_RBP_ID_22252701,Human_RBP_ID_22426385,Human_RBP_ID_22477704,Human_RBP_ID_22505788,Human_RBP_ID_22816725,Human_RBP_ID_22994464,Human_RBP_ID_23879165,Human_RBP_ID_24376443,Human_RBP_ID_24553078,Human_RBP_ID_26667644,Human_RBP_ID_27013474,Human_RBP_ID_27291307,Human_RBP_ID_27840029 Human_miRNA_ID_2394361 RMVar_hsa_circ_98453,RMVar_hsa_circ_200593 103394 RMVar_ID_103394 Human_SNP_ID_74717618 m1A Human chr2 - 61853956 61853956 61853956 GGTAAATCCCATCACTGGAGCGCGGGTCGCCCAGTACGAACGCGAAGACCCCTTAAAGGCCCTGG GGTAAATCCCATCACTGGAGCGCGGGTCGCCCGGTACGAACGCGAAGACCCCTTAAAGGCCCTGG T C FAM161A Ensembl:ENSG00000170264 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61853909..61854014 26863196 MeRIP-seq:(Medium) rs763794474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553228 Human_Splice_Rec_251767,Human_Splice_Rec_251779,Human_Splice_Rec_251789,Human_Splice_Rec_251803,Human_Splice_Rec_251817 103395 RMVar_ID_103395 Human_SNP_ID_74722452 m1A Human chr2 + 61870562 61870562 61870562 CCTTTATCCCGGGATTACTCCTGATGGCCTCTAACAGGCATCCTTACTTCCAGTCTTCCCTTCTT CCTTTATCCCGGGATTACTCCTGATGGCCTCTTACAGGCATCCTTACTTCCAGTCTTCCCTTCTT A T AC107081.2 Ensembl:ENSG00000236498 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:61870519..61870608 26863196 MeRIP-seq:(Medium) rs983649062 Functional Loss SNV dbSNP153 33..33 33 - - - 103396 RMVar_ID_103396 Human_SNP_ID_74728344 m1A Human chr2 - 61888447 61888442 61888448 GGGCGACTGCCGGGGCTGCCGGCGGCCGCGGGAAAGGCGCCTATCAGGACCGCGACAAGCCAGCC GGGCGACTGCCGGGGCTGCCGGCGGCCGCGG______CGCCTATCAGGACCGCGACAAGCCAGCC GCCTTTC G CCT4 Ensembl:ENSG00000115484 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr2:61888401..61888500;chr2:61888401..61888650 26863196 MeRIP-seq:(Medium) rs775189701 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_553296,Human_RBP_ID_4613217,Human_RBP_ID_9330474,Human_RBP_ID_22075354,Human_RBP_ID_22449810,Human_RBP_ID_22533582,Human_RBP_ID_23310874,Human_RBP_ID_23879332 Human_Splice_Rec_251827,Human_Splice_Rec_251853,Human_Splice_Rec_251883 103397 RMVar_ID_103397 Human_SNP_ID_74728363 m1A Human chr2 + 61888472 61888472 61888472 GCGCCTTTCCCGCGGCCGCCGGCAGCCCCGGCAGTCGCCCCGCTCCGGGGTGCCACATTCTCGGG GCGCCTTTCCCGCGGCCGCCGGCAGCCCCGGCTGTCGCCCCGCTCCGGGGTGCCACATTCTCGGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:61888376..61888605 26863410 MeRIP-seq:(Medium) rs1273022351 Functional Loss SNV dbSNP153 33..33 33 - - - 103398 RMVar_ID_103398 Human_SNP_ID_74728378 m1A Human chr2 + 61888494 61888494 61888494 CAGCCCCGGCAGTCGCCCCGCTCCGGGGTGCCACATTCTCGGGCATGGCAAACTCCGCTGTGTCT CAGCCCCGGCAGTCGCCCCGCTCCGGGGTGCCGCATTCTCGGGCATGGCAAACTCCGCTGTGTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:61888444..61888650 26863196 MeRIP-seq:(Medium) rs1478626631 Functional Loss SNV dbSNP153 33..33 33 - - - 103399 RMVar_ID_103399 Human_SNP_ID_74733131 m1A Human chr2 + 61905727 61905727 61905727 TTGAGGGTGGCAAACCCCTGAGCGGGCTGCTGAATGCGCTGGCCCAGGACACTTTCCACGGGTAC TTGAGGGTGGCAAACCCCTGAGCGGGCTGCTGCATGCGCTGGCCCAGGACACTTTCCACGGGTAC A C COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61905676..61905807 26863196 MeRIP-seq:(Medium) rs144687207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623337,Human_RBP_ID_22997353 Human_miRNA_ID_2038618,Human_miRNA_ID_2661099,Human_miRNA_ID_2679553,Human_miRNA_ID_3017600 RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 103400 RMVar_ID_103400 Human_SNP_ID_74733139 m1A Human chr2 - 61905734 61905734 61905734 TGCCGGGGTACCCGTGGAAAGTGTCCTGGGCCAGCGCATTCAGCAGCCCGCTCAGGGGTTTGCCA TGCCGGGGTACCCGTGGAAAGTGTCCTGGGCCTGCGCATTCAGCAGCCCGCTCAGGGGTTTGCCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:61905688..61905792 26863196 MeRIP-seq:(Medium) rs1382808152 Functional Loss SNV dbSNP153 33..33 33 - - - 103401 RMVar_ID_103401 Human_SNP_ID_74733143 m1A Human chr2 + 61905752 61905752 61905752 GCTGCTGAATGCGCTGGCCCAGGACACTTTCCACGGGTACCCCGGCATCACAGAGGAGCTGCTAC GCTGCTGAATGCGCTGGCCCAGGACACTTTCCCCGGGTACCCCGGCATCACAGAGGAGCTGCTAC A C COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:61905702..61905813 26863196 MeRIP-seq:(Medium) rs1194195918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1301817,Human_RBP_ID_4623337,Human_RBP_ID_18763616,Human_RBP_ID_22252754,Human_RBP_ID_22997353 RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 103402 RMVar_ID_103402 Human_SNP_ID_74737981 m1A Human chr2 - 61924351 61924348 61924351 CCCCCCTCCGACTCTGAGTCCTCCCTACCACCACCCCTTACTCGTTCTCAAGCCCAACACGCCCA CCCCCCTCCGACTCTGAGTCCTCCCTACCACC___CCTTACTCGTTCTCAAGCCCAACACGCCCA GGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:61924348..61924623 26863196 MeRIP-seq:(Medium) rs373414881 Functional Loss DEL dbSNP153 33..35 33 - - - 103403 RMVar_ID_103403 Human_SNP_ID_74737983 m1A Human chr2 - 61924354 61924354 61924354 CATCCCCCCTCCGACTCTGAGTCCTCCCTACCACCACCCCTTACTCGTTCTCAAGCCCAACACGC CATCCCCCCTCCGACTCTGAGTCCTCCCTACCCCCACCCCTTACTCGTTCTCAAGCCCAACACGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:61924344..61924447 26863196 MeRIP-seq:(Medium) rs1297757718 Functional Loss SNV dbSNP153 33..33 33 - - - 103404 RMVar_ID_103404 Human_SNP_ID_74804848 m1A Human chr2 + 62196205 62196196 62196205 AGAGCCAAGCCGGAGCAGTCCCTGCCGCCGACACCGCCGGGCCGCCCGTCCGGGGCGCCGCGCAT AGAGCCAAGCCGGAGCAGTCCCTG_________CCGCCGGGCCGCCCGTCCGGGGCGCCGCGCAT GCCGCCGACA G B3GNT2 Ensembl:ENSG00000170340 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:62196167..62196350 26863196 MeRIP-seq:(Medium) rs990122239 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4613255,Human_RBP_ID_5146558,Human_RBP_ID_18421795 103405 RMVar_ID_103405 Human_SNP_ID_74806405 m1A Human chr2 + 62202458 62202458 62202458 TCCATTGGGTTTGGAGTGCATGGTGCTTAGAAAGGTGTAATAGGCCATGATGCAATCTCGGGGAT TCCATTGGGTTTGGAGTGCATGGTGCTTAGAAGGGTGTAATAGGCCATGATGCAATCTCGGGGAT A G B3GNT2 Ensembl:ENSG00000170340 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:62202456..62202557 26863196 MeRIP-seq:(Medium) rs1233567626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2656218 103406 RMVar_ID_103406 Human_SNP_ID_74807301 m1A Human chr2 + 62205989 62205989 62205989 ATCGATGGACTGGGGGAATCAAGGCTGTCCTCATGGAAGAGGAGACAGGATTTGAACCTGGGCCT ATCGATGGACTGGGGGAATCAAGGCTGTCCTCCTGGAAGAGGAGACAGGATTTGAACCTGGGCCT A C B3GNT2 Ensembl:ENSG00000170340 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:62205983..62206106 26863196 MeRIP-seq:(Medium) rs1033888466 Functional Loss SNV dbSNP153 33..33 33 - - - 103407 RMVar_ID_103407 Human_SNP_ID_74934682 m1A Human chr2 - 62705983 62705983 62705983 CCTTCTCATAGCCGCTCCTCCGTCGCCGCCGCAGCAGCAGCCGCCGCCGCCACCGAGTCCTCCAT CCTTCTCATAGCCGCTCCTCCGTCGCCGCCGCCGCAGCAGCCGCCGCCGCCACCGAGTCCTCCAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:62705685..62706107;chr2:62705801..62706005 26863196 MeRIP-seq:(Medium) rs990621339 Functional Loss SNV dbSNP153 33..33 33 - - - 103408 RMVar_ID_103408 Human_SNP_ID_74940578 m1A Human chr2 + 62730826 62730823 62730827 AGAGATGGACAGAGACAGAGAGAAAAAGAAAGAGAGAAACAGAGAGACGGAGAGAGAGAGACAGA AGAGATGGACAGAGACAGAGAGAAAAAGAA____AGAAACAGAGAGACGGAGAGAGAGAGACAGA AAGAG A EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:62730693..62730865 26863196 MeRIP-seq:(Medium) rs1164810429 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_54338,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_361104,RMVar_hsa_circ_62128 103409 RMVar_ID_103409 Human_SNP_ID_74940579 m1A Human chr2 + 62730826 62730823 62730827 AGAGATGGACAGAGACAGAGAGAAAAAGAAAGAGAGAAACAGAGAGACGGAGAGAGAGAGACAGA AGAGATGGACAGAGACAGAGAGAAAAAGAAAG__AGAAACAGAGAGACGGAGAGAGAGAGACAGA AAGAG AAG EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:62730693..62730865 26863196 MeRIP-seq:(Medium) rs1164810429 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_54338,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_361104,RMVar_hsa_circ_62128 103410 RMVar_ID_103410 Human_SNP_ID_74940616 m1A Human chr2 + 62730858 62730858 62730858 AGAGAAACAGAGAGACGGAGAGAGAGAGACAGACAGGCAGACAGGCAGGCAGAGAAAGAGTAAGA AGAGAAACAGAGAGACGGAGAGAGAGAGACAGGCAGGCAGACAGGCAGGCAGAGAAAGAGTAAGA A G EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:62730722..62730899 26863196 MeRIP-seq:(Medium) rs987859011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54338,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_361104,RMVar_hsa_circ_62128 103411 RMVar_ID_103411 Human_SNP_ID_74950953 m1A Human chr2 + 62772244 62772244 62772244 GAGAGAAGGAGAGAAAGAGAAGGAAGGAAGGAAGGGCGGGGCTTTAACTGTTTATTTGGGTTGAG GAGAGAAGGAGAGAAAGAGAAGGAAGGAAGGAGGGGCGGGGCTTTAACTGTTTATTTGGGTTGAG A G EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:62772232..62772297 26863196 MeRIP-seq:(Medium) rs564730345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8200538,Human_RBP_ID_21932093,Human_RBP_ID_23282664,Human_RBP_ID_26786959 RMVar_hsa_circ_54338,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_361104,RMVar_hsa_circ_62128,RMVar_hsa_circ_5814,RMVar_hsa_circ_360001,RMVar_hsa_circ_64389,RMVar_hsa_circ_68960,RMVar_hsa_circ_318380 103412 RMVar_ID_103412 Human_SNP_ID_75016809 m1A Human chr2 - 63052956 63052955 63052956 TAACAGCTGGGTGGAGGCGCCCCGACGGATCCAGGGGGCCCGGGGCCAGGAGCGGTGCAGGGCTC TAACAGCTGGGTGGAGGCGCCCCGACGGATCC_GGGGGCCCGGGGCCAGGAGCGGTGCAGGGCTC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:63052910..63053110 26863196 MeRIP-seq:(Medium) rs1559118818 Functional Loss DEL dbSNP153 33..33 33 - - - 103413 RMVar_ID_103413 Human_SNP_ID_75017751 m1A Human chr2 + 63056055 63056055 63056055 CATCACCACCCGCACCAGCTCAGCCCCATGGCACCCTCCTCCATGGCGGGCCACCATCATCACCA CATCACCACCCGCACCAGCTCAGCCCCATGGCCCCCTCCTCCATGGCGGGCCACCATCATCACCA A C OTX1 Ensembl:ENSG00000115507 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:63055842..63056142 26863196 MeRIP-seq:(Medium) rs1486513192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17279023 103414 RMVar_ID_103414 Human_SNP_ID_75068471 m1A Human chr2 + 63271813 63271813 63271813 AGCATGACATCAGGCCCACCCCGCCTGCTGCCACTACTGCTGCCAACATCAACCTACATGTGCCA AGCATGACATCAGGCCCACCCCGCCTGCTGCCGCTACTGCTGCCAACATCAACCTACATGTGCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:63271710..63271853 26863196 MeRIP-seq:(Medium) rs1475805625 Functional Loss SNV dbSNP153 33..33 33 - - - 103415 RMVar_ID_103415 Human_SNP_ID_75114541 m1A Human chr2 + 63470051 63470051 63470051 AAACTTGGTTTCCAGGACACCACACTCCCTTCATTGTGCTCTACTTCTCTAGCTACTCCATTCTG AAACTTGGTTTCCAGGACACCACACTCCCTTCGTTGTGCTCTACTTCTCTAGCTACTCCATTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:63470030..63470165 26863196 MeRIP-seq:(Medium) rs1246537117 Functional Loss SNV dbSNP153 33..33 33 - - - 103416 RMVar_ID_103416 Human_SNP_ID_75151725 m1A Human chr2 - 63622383 63622383 63622383 CTCCAGAGCTGTCCAGGAATTTGGTCTTGCCCAGTTCAAAAGCAACGTGACCAAGACTATGAAGG CTCCAGAGCTGTCCAGGAATTTGGTCTTGCCCGGTTCAAAAGCAACGTGACCAAGACTATGAAGG T C WDPCP,AC016734.1 Ensembl:ENSG00000143951,Ensembl:ENSG00000228305 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs878899773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853028 103417 RMVar_ID_103417 Human_SNP_ID_75151783 m1A Human chr2 - 63622594 63622594 63622594 TATTTCCTGCCAATGTTGCTCACTCGGTGTACATCCTGGAGGACTCTATTGTGGACCCACAGAAT TATTTCCTGCCAATGTTGCTCACTCGGTGTACGTCCTGGAGGACTCTATTGTGGACCCACAGAAT T C WDPCP,AC016734.1 Ensembl:ENSG00000143951,Ensembl:ENSG00000228305 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs900136906 Functional Loss SNV dbSNP153 33..33 33 - - - 103418 RMVar_ID_103418 Human_SNP_ID_75201125 m1A Human chr2 - 63841049 63841049 63841049 CCCAGCTGCTAACCCCCCCTTGTCCACCCGTCAGCCGGCTCCCGACACCCACAGCCCCTACTTTC CCCAGCTGCTAACCCCCCCTTGTCCACCCGTCGGCCGGCTCCCGACACCCACAGCCCCTACTTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:63840939..63841715 26863196 MeRIP-seq:(Medium) rs1259171565 Functional Loss SNV dbSNP153 33..33 33 - - - 103419 RMVar_ID_103419 Human_SNP_ID_75201147 m1A Human chr2 - 63841092 63841092 63841092 CCCTCACACATGCACACCTTGAGCCCCTCCCTAACGGTCGCAGCCCAGCTGCTAACCCCCCCTTG CCCTCACACATGCACACCTTGAGCCCCTCCCTGACGGTCGCAGCCCAGCTGCTAACCCCCCCTTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:63841041..63841173 26863196 MeRIP-seq:(Medium) rs1259917931 Functional Loss SNV dbSNP153 33..33 33 - - - 103420 RMVar_ID_103420 Human_SNP_ID_75205225 m1A Human chr2 + 63856364 63856364 63856364 GGTGCTTCTCAGTTCCAAGAAGTCATTCGGCAAGAGCTAGAATTATCTGTGAAGAAGGAACTAGA GGTGCTTCTCAGTTCCAAGAAGTCATTCGGCAGGAGCTAGAATTATCTGTGAAGAAGGAACTAGA A G UGP2 Ensembl:ENSG00000169764 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:63856257..63856376 26863196 MeRIP-seq:(Medium) rs1364602786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1588909,Human_RBP_ID_1921641,Human_RBP_ID_18763901,Human_RBP_ID_24546463,Human_RBP_ID_26819797 Human_Splice_Rec_253086,Human_Splice_Rec_253087,Human_Splice_Rec_253104,Human_Splice_Rec_253105,Human_Splice_Rec_253116,Human_Splice_Rec_253120,Human_Splice_Rec_253121,Human_Splice_Rec_253128,Human_Splice_Rec_253129,Human_Splice_Rec_253146,Human_Splice_Rec_253147,Human_Splice_Rec_253160,Human_Splice_Rec_253162,Human_Splice_Rec_253163,Human_Splice_Rec_253178,Human_Splice_Rec_253179,Human_Splice_Rec_253190,Human_Splice_Rec_253191,Human_Splice_Rec_253198,Human_Splice_Rec_253199,Human_Splice_Rec_253206,Human_Splice_Rec_253207,Human_Splice_Rec_253238,Human_Splice_Rec_253239,Human_Splice_Rec_253242,Human_Splice_Rec_253243,Human_Splice_Rec_253250,Human_Splice_Rec_253251,Human_Splice_Rec_253256,Human_Splice_Rec_253257,Human_Splice_Rec_253260,Human_Splice_Rec_253261,Human_Splice_Rec_253264,Human_Splice_Rec_253265,Human_Splice_Rec_253272,Human_Splice_Rec_253273,Human_Splice_Rec_253292,Human_Splice_Rec_253293,Human_Splice_Rec_253302,Human_Splice_Rec_253303,Human_Splice_Rec_253312,Human_Splice_Rec_253313,Human_Splice_Rec_253320,Human_Splice_Rec_253321,Human_Splice_Rec_253332,Human_Splice_Rec_253333,Human_Splice_Rec_253342,Human_Splice_Rec_253343,Human_Splice_Rec_253349,Human_Splice_Rec_253365,Human_Splice_Rec_253367 RMVar_hsa_circ_95339,RMVar_hsa_circ_108520,RMVar_hsa_circ_200696,RMVar_hsa_circ_200701,RMVar_hsa_circ_272581,RMVar_hsa_circ_291888,RMVar_hsa_circ_368069,RMVar_hsa_circ_200697,RMVar_hsa_circ_324287,RMVar_hsa_circ_272648,RMVar_hsa_circ_97206,RMVar_hsa_circ_270110,RMVar_hsa_circ_200702,RMVar_hsa_circ_200703,RMVar_hsa_circ_200699,RMVar_hsa_circ_200700,RMVar_hsa_circ_200698 103421 RMVar_ID_103421 Human_SNP_ID_75242199 m1A Human chr2 - 63990275 63990275 63990275 ACTGGCTCTTCGTGAAAAGAAACAAGGTCAGCAGGGGGTAACGTTAAGCCAAAGTCACCAGAGTT ACTGGCTCTTCGTGAAAAGAAACAAGGTCAGCTGGGGGTAACGTTAAGCCAAAGTCACCAGAGTT T A VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:63990271..63990702 26863196 MeRIP-seq:(Medium) rs948727943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94668,RMVar_hsa_circ_200722 103422 RMVar_ID_103422 Human_SNP_ID_75353973 m1A Human chr2 + 64454554 64454554 64454554 TACCCCGCCGCGCCGGGCAAGAAGATGGCGGGATCAGTGGCCGACAGCGATGCCGTGGTGGTGAG TACCCCGCCGCGCCGGGCAAGAAGATGGCGGGTTCAGTGGCCGACAGCGATGCCGTGGTGGTGAG A T LGALSL Ensembl:ENSG00000119862 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:64454429..64454613 26863196 MeRIP-seq:(Medium) rs767522314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553552,Human_RBP_ID_4613555 Human_Splice_Rec_253663,Human_Splice_Rec_253669,Human_Splice_Rec_253677,Human_Splice_Rec_253681,Human_Splice_Rec_253689 103423 RMVar_ID_103423 Human_SNP_ID_75353978 m1A Human chr2 - 64454559 64454559 64454559 CCACACTCACCACCACGGCATCGCTGTCGGCCACTGATCCCGCCATCTTCTTGCCCGGCGCGGCG CCACACTCACCACCACGGCATCGCTGTCGGCCGCTGATCCCGCCATCTTCTTGCCCGGCGCGGCG T C LGALSL-DT,LGALSL-DT:2 RNACentral:URS0000D5DE77,RNACentral:URS0000D576ED lincRNA,lincRNA exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:64454393..64454600 26863410 MeRIP-seq:(Medium) rs748002648 Functional Loss SNV dbSNP153 33..33 33 - - - 103424 RMVar_ID_103424 Human_SNP_ID_75371155 m1A Human chr2 + 64524404 64524404 64524404 GGAGGAGGTGGAGGAGGCGGCGGCGGCGGCGGAAGAGGGCGGAGGGTAGTGGGATGGGGGTCCCG GGAGGAGGTGGAGGAGGCGGCGGCGGCGGCGGCAGAGGGCGGAGGGTAGTGGGATGGGGGTCCCG A C AFTPH Ensembl:ENSG00000119844 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:64524351..64551483;chr2:64524354..64551533 26863196 MeRIP-seq:(Medium) rs1047010389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4613594,Human_RBP_ID_5527700,Human_RBP_ID_8851901 103425 RMVar_ID_103425 Human_SNP_ID_75371234 m1A Human chr2 - 64524576 64524576 64524576 CTCCTTCGGGGCGGCTGCGATGGGCATGGCTCAGGGGCCCGGGGAGGAACTGACTCCCCGGGGAA CTCCTTCGGGGCGGCTGCGATGGGCATGGCTCCGGGGCCCGGGGAGGAACTGACTCCCCGGGGAA T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:64524396..64524625 26863196 MeRIP-seq:(Medium) rs1377598735 Functional Loss SNV dbSNP153 33..33 33 - - - 103426 RMVar_ID_103426 Human_SNP_ID_75399974 m1A Human chr2 + 64636495 64636494 64636495 CGAGCAGTGAGGCCGGGGTGAGGCAGGCCTCCAGGGGCGTAGTGCTTCCGAGGTCGCAGGGGTGG CGAGCAGTGAGGCCGGGGTGAGGCAGGCCTCC_GGGGCGTAGTGCTTCCGAGGTCGCAGGGGTGG CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:64636446..64636561 26863196 MeRIP-seq:(Medium) rs1251543993 Functional Loss DEL dbSNP153 33..33 33 - - - 103427 RMVar_ID_103427 Human_SNP_ID_75399975 m1A Human chr2 + 64636495 64636495 64636495 CGAGCAGTGAGGCCGGGGTGAGGCAGGCCTCCAGGGGCGTAGTGCTTCCGAGGTCGCAGGGGTGG CGAGCAGTGAGGCCGGGGTGAGGCAGGCCTCCGGGGGCGTAGTGCTTCCGAGGTCGCAGGGGTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:64636446..64636561 26863196 MeRIP-seq:(Medium) rs750018718 Functional Loss SNV dbSNP153 33..33 33 - - - 103428 RMVar_ID_103428 Human_SNP_ID_75404194 m1A Human chr2 + 64653444 64653444 64653444 CGAGAGCGCGGGGCCCGGACCGGGGCCGCGGGAGGGAGCGCTCCTCCCGTACCTGCTCCGTCCCC CGAGAGCGCGGGGCCCGGACCGGGGCCGCGGGGGGGAGCGCTCCTCCCGTACCTGCTCCGTCCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:64653423..64653594 26863196 MeRIP-seq:(Medium) rs985261968 Functional Loss SNV dbSNP153 33..33 33 - - - 103429 RMVar_ID_103429 Human_SNP_ID_75413402 m1A Human chr2 + 64693836 64693836 64693836 CATTCTACTTCTTACCTTTCCCTGCCTCTGGTAACCTTCATTCTACTCCTTACCTCCACCATCTG CATTCTACTTCTTACCTTTCCCTGCCTCTGGTGACCTTCATTCTACTCCTTACCTCCACCATCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:64693802..64693867 26863196 MeRIP-seq:(Medium) rs116044400 Functional Loss SNV dbSNP153 33..33 33 - - - 103430 RMVar_ID_103430 Human_SNP_ID_75427023 m1A Human chr2 + 64750759 64750759 64750759 GGAAGTTGCAGCGGCTCCCGAGGAGGAGGAGGAGAAGGAGGAGGAGGATGTTACACCGTAACAAG GGAAGTTGCAGCGGCTCCCGAGGAGGAGGAGGTGAAGGAGGAGGAGGATGTTACACCGTAACAAG A T lnc-AFTPH-5 RNACentral:URS0000D58305 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:64750604..64750897 26863196 MeRIP-seq:(Medium) rs71424131 Functional Loss SNV dbSNP153 33..33 33 - - - 103431 RMVar_ID_103431 Human_SNP_ID_75427053 m1A Human chr2 + 64750814 64750814 64750814 CCGTAACAAGTACAGACAGACAGCCATGGATCAGAGGGGCGCTGCAAGCAGGAGCAGGGGCGGCC CCGTAACAAGTACAGACAGACAGCCATGGATCCGAGGGGCGCTGCAAGCAGGAGCAGGGGCGGCC A C lnc-AFTPH-5 RNACentral:URS0000D58305 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:64750763..64750846 26863196 MeRIP-seq:(Medium) rs903255965 Functional Loss SNV dbSNP153 33..33 33 - - - 103432 RMVar_ID_103432 Human_SNP_ID_75427054 m1A Human chr2 + 64750814 64750814 64750814 CCGTAACAAGTACAGACAGACAGCCATGGATCAGAGGGGCGCTGCAAGCAGGAGCAGGGGCGGCC CCGTAACAAGTACAGACAGACAGCCATGGATCTGAGGGGCGCTGCAAGCAGGAGCAGGGGCGGCC A T lnc-AFTPH-5 RNACentral:URS0000D58305 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:64750763..64750846 26863196 MeRIP-seq:(Medium) rs903255965 Functional Loss SNV dbSNP153 33..33 33 - - - 103433 RMVar_ID_103433 Human_SNP_ID_75511003 m1A Human chr2 - 65088142 65088141 65088142 GGCATGTTTAGATGTCAGGTTTAGTCTTCTGAAGATGAAGTTCAGCCATTTTGTATCAAACAGCA GGCATGTTTAGATGTCAGGTTTAGTCTTCTGA_GATGAAGTTCAGCCATTTTGTATCAAACAGCA CT C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:65088071..65088170 32194978 MeRIP-seq:(Medium) rs1371779458 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_281000,Human_RBP_ID_553722,Human_RBP_ID_1023828,Human_RBP_ID_1921804,Human_RBP_ID_2658287,Human_RBP_ID_3631538,Human_RBP_ID_5147096,Human_RBP_ID_6940343,Human_RBP_ID_8523272,Human_RBP_ID_8948476,Human_RBP_ID_9109693,Human_RBP_ID_9993805,Human_RBP_ID_13940311,Human_RBP_ID_17508272,Human_RBP_ID_22393924,Human_RBP_ID_23211592,Human_RBP_ID_23880284,Human_RBP_ID_24422241,Human_RBP_ID_26487160,Human_RBP_ID_27291570,Human_RBP_ID_27481189,Human_RBP_ID_27697594 RMVar_hsa_circ_200774 103434 RMVar_ID_103434 Human_SNP_ID_75513518 m1A Human chr2 - 65098058 65098058 65098058 ATTGTTAATTATTTCCCCCTTCAGGATGATACATATACAGAAAGCTACATCAGCACAATTGGTGT ATTGTTAATTATTTCCCCCTTCAGGATGATACGTATACAGAAAGCTACATCAGCACAATTGGTGT T C RAB1A Ensembl:ENSG00000138069 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:65098008..65130057 32194978 MeRIP-seq:(Medium) rs1308012001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17277706,Human_RBP_ID_22765035 Human_Splice_Rec_253948,Human_Splice_Rec_253949,Human_Splice_Rec_253966,Human_Splice_Rec_253967,Human_Splice_Rec_253982,Human_Splice_Rec_253983 RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200778,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777,RMVar_hsa_circ_278839 103435 RMVar_ID_103435 Human_SNP_ID_75522466 m1A Human chr2 - 65129725 65129725 65129725 GGCCGGGAGTCGGGCCCCATTGTCTGACGCGGAGGGGCGGCCGCGCGGGGGAGGGGTCGGGCCGG GGCCGGGAGTCGGGCCCCATTGTCTGACGCGGGGGGGCGGCCGCGCGGGGGAGGGGTCGGGCCGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:65129716..65129821 26863196 MeRIP-seq:(Medium) rs1212186947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638723,Human_RBP_ID_8110206,Human_RBP_ID_8200546,Human_RBP_ID_17140084,Human_RBP_ID_22721976,Human_RBP_ID_26786977 RMVar_hsa_circ_200774 103436 RMVar_ID_103436 Human_SNP_ID_75522467 m1A Human chr2 - 65129725 65129725 65129725 GGCCGGGAGTCGGGCCCCATTGTCTGACGCGGAGGGGCGGCCGCGCGGGGGAGGGGTCGGGCCGG GGCCGGGAGTCGGGCCCCATTGTCTGACGCGGCGGGGCGGCCGCGCGGGGGAGGGGTCGGGCCGG T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:65129716..65129821 26863196 MeRIP-seq:(Medium) rs1212186947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3638723,Human_RBP_ID_8110206,Human_RBP_ID_8200546,Human_RBP_ID_17140084,Human_RBP_ID_22721976,Human_RBP_ID_26786977 RMVar_hsa_circ_200774 103437 RMVar_ID_103437 Human_SNP_ID_75522548 m1A Human chr2 + 65129912 65129912 65129912 CTCCTGAACTCACTATTCGGGATTCATGCTGGACATGTCACTGCAGCTGCCGCCGCCGCCACCGC CTCCTGAACTCACTATTCGGGATTCATGCTGGGCATGTCACTGCAGCTGCCGCCGCCGCCACCGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:65089056..65130008 32194978 MeRIP-seq:(Medium) rs907769758 Functional Loss SNV dbSNP153 33..33 33 - - - 103438 RMVar_ID_103438 Human_SNP_ID_75522549 m1A Human chr2 + 65129912 65129912 65129912 CTCCTGAACTCACTATTCGGGATTCATGCTGGACATGTCACTGCAGCTGCCGCCGCCGCCACCGC CTCCTGAACTCACTATTCGGGATTCATGCTGGTCATGTCACTGCAGCTGCCGCCGCCGCCACCGC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:65089056..65130008 32194978 MeRIP-seq:(Medium) rs907769758 Functional Loss SNV dbSNP153 33..33 33 - - - 103439 RMVar_ID_103439 Human_SNP_ID_75522584 m1A Human chr2 - 65129954 65129954 65129954 GTGGCGCGGAGAGTCAGGGCGGCGGCTGCGGCAGCAAGGGCGGCGGTGGCGGCGGCGGCAGCTGC GTGGCGCGGAGAGTCAGGGCGGCGGCTGCGGCCGCAAGGGCGGCGGTGGCGGCGGCGGCAGCTGC T G RAB1A Ensembl:ENSG00000138069 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:65129907..65130100 26863196 MeRIP-seq:(Medium) rs1451192246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553743,Human_RBP_ID_777007,Human_RBP_ID_4624370,Human_RBP_ID_22451318,Human_RBP_ID_23880389 Human_Splice_Rec_253945,Human_Splice_Rec_253959,Human_Splice_Rec_253963,Human_Splice_Rec_253973,Human_Splice_Rec_253979,Human_Splice_Rec_253985 RMVar_hsa_circ_200774 103440 RMVar_ID_103440 Human_SNP_ID_75522592 m1A Human chr2 - 65129993 65129993 65129993 CCCGGAACAGCCTATCTCATTCCTTTCTTTCGATTACCCGTGGCGCGGAGAGTCAGGGCGGCGGC CCCGGAACAGCCTATCTCATTCCTTTCTTTCGTTTACCCGTGGCGCGGAGAGTCAGGGCGGCGGC T A RAB1A Ensembl:ENSG00000138069 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:65129926..65130092 26863196 MeRIP-seq:(Medium) rs925548502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243344,Human_RBP_ID_553744,Human_RBP_ID_1378809,Human_RBP_ID_4613868,Human_RBP_ID_5423207,Human_RBP_ID_5445038,Human_RBP_ID_5470972,Human_RBP_ID_5502457,Human_RBP_ID_6975818,Human_RBP_ID_13941316,Human_RBP_ID_17017080,Human_RBP_ID_17959748,Human_RBP_ID_22451318,Human_RBP_ID_22816021,Human_RBP_ID_23282163,Human_RBP_ID_23880389 RMVar_hsa_circ_200774 103441 RMVar_ID_103441 Human_SNP_ID_75522618 m1A Human chr2 - 65130066 65130062 65130066 TGGAAGCGATAGCTGAGTGGCGGCGGCTGCTGATTGTGTTCTAGGGGACGGAGTAGGGGAAGACG TGGAAGCGATAGCTGAGTGGCGGCGGCTGCTG____TGTTCTAGGGGACGGAGTAGGGGAAGACG ACAAT A RAB1A Ensembl:ENSG00000138069 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:65129876..65130125 26863196 MeRIP-seq:(Medium) rs1292299148 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_553745,Human_RBP_ID_4624372,Human_RBP_ID_5423210,Human_RBP_ID_5470974,Human_RBP_ID_6940541,Human_RBP_ID_8233942,Human_RBP_ID_18421806,Human_RBP_ID_22252912,Human_RBP_ID_22449825,Human_RBP_ID_23880390 103442 RMVar_ID_103442 Human_SNP_ID_75522619 m1A Human chr2 + 65130068 65130068 65130068 TCTTCCCCTACTCCGTCCCCTAGAACACAATCAGCAGCCGCCGCCACTCAGCTATCGCTTCCACC TCTTCCCCTACTCCGTCCCCTAGAACACAATCGGCAGCCGCCGCCACTCAGCTATCGCTTCCACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:65129876..65130125;chr2:65129626..65130254;chr2:65129607..65130125;chr2:65097976..65130125 26863196 MeRIP-seq:(Medium) rs1362125130 Functional Loss SNV dbSNP153 33..33 33 - - - 103443 RMVar_ID_103443 Human_SNP_ID_75542609 m1A Human chr2 + 65205001 65205001 65205001 GAAAGCCCTTCACTTCGCCCTCCAGCTGCTGCAGCTGCAGCCCGACCGCGAGCGTGCCAAGCGGC GAAAGCCCTTCACTTCGCCCTCCAGCTGCTGCTGCTGCAGCCCGACCGCGAGCGTGCCAAGCGGC A T lnc-ACTR2-11 RNACentral:URS0000D5769C lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:65204976..65205097;chr2:65204976..65205050 26863196 MeRIP-seq:(Medium) rs1032786518 Functional Loss SNV dbSNP153 33..33 33 - - - 103444 RMVar_ID_103444 Human_SNP_ID_75542765 m1A Human chr2 + 65205711 65205711 65205711 CACACTAATGTCAATGATGGGACAGAATTTGGAGGATCAATTTATCAGAAAGTTTGTGAAGATCT CACACTAATGTCAATGATGGGACAGAATTTGGTGGATCAATTTATCAGAAAGTTTGTGAAGATCT A T AC007318.1 Ensembl:ENSG00000172974 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs887660946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1589040,Human_RBP_ID_1921841,Human_RBP_ID_6961783,Human_RBP_ID_8258692,Human_RBP_ID_8523321,Human_RBP_ID_17277710,Human_RBP_ID_17394140,Human_RBP_ID_18167381,Human_RBP_ID_18534078,Human_RBP_ID_22765036 103445 RMVar_ID_103445 Human_SNP_ID_75548344 m1A Human chr2 - 65227865 65227865 65227865 GAAGAGCCGCTGCAGCCGCACAACCTACAGCCACCGCCGCCCGGCCGTTTTCTCTTCTTCCTCTT GAAGAGCCGCTGCAGCCGCACAACCTACAGCCGCCGCCGCCCGGCCGTTTTCTCTTCTTCCTCTT T C lnc-RAB1A-11,lnc-RAB1A-11:2 RNACentral:URS0000D5AC5E,RNACentral:URS00008B895C lincRNA,lincRNA intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:65227776..65227975 26863196 MeRIP-seq:(Medium) rs903798129 Functional Loss SNV dbSNP153 33..33 33 - - - 103446 RMVar_ID_103446 Human_SNP_ID_75551674 m1A Human chr2 - 65239802 65239802 65239802 AATAAAAGTGGGTTAGCATCAGGATATTTACTATATTTTAAGACAGCATCTGAAAAATATCACTT AATAAAAGTGGGTTAGCATCAGGATATTTACTGTATTTTAAGACAGCATCTGAAAAATATCACTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:65239800..65239975 26863196 MeRIP-seq:(Medium) rs747180985 Functional Loss SNV dbSNP153 33..33 33 - - - 103447 RMVar_ID_103447 Human_SNP_ID_75558457 m1A Human chr2 + 65266607 65266607 65266607 GAGAAATGATAGGATCTGATGTATATTTTTAAAGGATCATTAAGTCTGGTGTGGTGAATAGACTC GAGAAATGATAGGATCTGATGTATATTTTTAAGGGATCATTAAGTCTGGTGTGGTGAATAGACTC A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:65266605..65266751 26863196 MeRIP-seq:(Medium) rs1378246549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81109,RMVar_hsa_circ_200786 103448 RMVar_ID_103448 Human_SNP_ID_75559467 m1A Human chr2 + 65270548 65270548 65270548 CTTTTGAGAACGGGGCTTGTTAAAGGACGCGTATGTAGGGCCCGTACCTACTGGCAGTTGGGTTC CTTTTGAGAACGGGGCTTGTTAAAGGACGCGTGTGTAGGGCCCGTACCTACTGGCAGTTGGGTTC A G ACTR2 Ensembl:ENSG00000138071 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553846,Human_RBP_ID_775831,Human_RBP_ID_6940947,Human_RBP_ID_8200552,Human_RBP_ID_13942051,Human_RBP_ID_23880532,Human_RBP_ID_26486403 RMVar_hsa_circ_81109,RMVar_hsa_circ_200786 103449 RMVar_ID_103449 Human_SNP_ID_75559468 m1A Human chr2 + 65270548 65270548 65270548 CTTTTGAGAACGGGGCTTGTTAAAGGACGCGTATGTAGGGCCCGTACCTACTGGCAGTTGGGTTC CTTTTGAGAACGGGGCTTGTTAAAGGACGCGTTTGTAGGGCCCGTACCTACTGGCAGTTGGGTTC A T ACTR2 Ensembl:ENSG00000138071 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_553846,Human_RBP_ID_775831,Human_RBP_ID_6940947,Human_RBP_ID_8200552,Human_RBP_ID_13942051,Human_RBP_ID_23880532,Human_RBP_ID_26486403 RMVar_hsa_circ_81109,RMVar_hsa_circ_200786 103450 RMVar_ID_103450 Human_SNP_ID_75570607 m1A Human chr2 - 65313731 65313731 65313731 CCGTGAGAACTTGCATCCGCCGGGTGAGCTGCATGTGGTGCGCGGACAGCATGCTCTATCACTGT CCGTGAGAACTTGCATCCGCCGGGTGAGCTGCGTGTGGTGCGCGGACAGCATGCTCTATCACTGT T C SPRED2 Ensembl:ENSG00000198369 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:65313680..65313875 32194978 MeRIP-seq:(Medium) rs1269855441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18764150,Human_RBP_ID_22076326,Human_RBP_ID_27481238 Human_miRNA_ID_205432,Human_miRNA_ID_2011396,Human_miRNA_ID_2757754 RMVar_hsa_circ_104607,RMVar_hsa_circ_200787 103451 RMVar_ID_103451 Human_SNP_ID_75593915 m1A Human chr2 - 65404848 65404848 65404848 GCTGTTGTTGGGGGAGGTGTTTGTTTGGCAGAAGGGAAAGGTGGTCTGTTCATGCTGGGGAGGTA GCTGTTGTTGGGGGAGGTGTTTGTTTGGCAGAGGGGAAAGGTGGTCTGTTCATGCTGGGGAGGTA T C SPRED2 Ensembl:ENSG00000198369 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:65404844..65404941 26863196 MeRIP-seq:(Medium) rs144751405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8523428,Human_RBP_ID_17207907,Human_RBP_ID_18494188,Human_RBP_ID_22699579 RMVar_hsa_circ_122122,RMVar_hsa_circ_200791,RMVar_hsa_circ_321419 103452 RMVar_ID_103452 Human_SNP_ID_75600476 m1A Human chr2 - 65432011 65432011 65432011 AAGATGAAGGGAGCAAAGCTGCCCGCCGCGGGACAGGCGTCTAGGTGAACAAGAAAATGACCGAA AAGATGAAGGGAGCAAAGCTGCCCGCCGCGGGGCAGGCGTCTAGGTGAACAAGAAAATGACCGAA T C SPRED2 Ensembl:ENSG00000198369 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:65431909..65432015 26863196 MeRIP-seq:(Medium) rs747229777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8942583,Human_RBP_ID_22996826,Human_RBP_ID_23115125,Human_RBP_ID_24546079,Human_RBP_ID_26339388 Human_Splice_Rec_254057,Human_Splice_Rec_254108,Human_Splice_Rec_254109 RMVar_hsa_circ_122122,RMVar_hsa_circ_200791,RMVar_hsa_circ_321419 103453 RMVar_ID_103453 Human_SNP_ID_75600605 m1A Human chr2 + 65432354 65432354 65432354 GGAGCGGCAGGGACTGCTGCGAGGAGGAGGAGAGCGCCGGCCGCGGGTGGGGGGGCTCAGTCCGG GGAGCGGCAGGGACTGCTGCGAGGAGGAGGAGGGCGCCGGCCGCGGGTGGGGGGGCTCAGTCCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:65432151..65432475 26863410 MeRIP-seq:(Medium) rs12185577 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13431,GWAS_ID_13432,GWAS_ID_13433,GWAS_ID_13434,GWAS_ID_13435,GWAS_ID_13436,GWAS_ID_13437,GWAS_ID_13438 103454 RMVar_ID_103454 Human_SNP_ID_75852764 m1A Human chr2 + 66435332 66435332 66435332 GGAGAGAAAGAAAGAGAGAGAGAGAAGAGAGAAACTGATTAGGAATTAGGACTGATTCAAGGGAA GGAGAGAAAGAAAGAGAGAGAGAGAAGAGAGAGACTGATTAGGAATTAGGACTGATTCAAGGGAA A G MEIS1 Ensembl:ENSG00000143995 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:66435176..66435466 26863196 MeRIP-seq:(Medium) rs1448873923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8523464,Human_RBP_ID_13942616 103455 RMVar_ID_103455 Human_SNP_ID_76096766 m1A Human chr2 - 67397409 67397409 67397409 GGCCCGCCTCCACCAGCCGCTTCTTCTTTCACATTTTGCAAAGGGATGAGTAGGGCAACAGCACT GGCCCGCCTCCACCAGCCGCTTCTTCTTTCACTTTTTGCAAAGGGATGAGTAGGGCAACAGCACT T A LINC01829 Ensembl:ENSG00000236780 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:67397359..67397668 26863196 MeRIP-seq:(Medium) rs1221205354 Functional Loss SNV dbSNP153 33..33 33 - - - 103456 RMVar_ID_103456 Human_SNP_ID_76096768 m1A Human chr2 - 67397411 67397411 67397411 ATGGCCCGCCTCCACCAGCCGCTTCTTCTTTCACATTTTGCAAAGGGATGAGTAGGGCAACAGCA ATGGCCCGCCTCCACCAGCCGCTTCTTCTTTCCCATTTTGCAAAGGGATGAGTAGGGCAACAGCA T G LINC01829 Ensembl:ENSG00000236780 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:67397360..67397624 26863196 MeRIP-seq:(Medium) rs1558577953 Functional Loss SNV dbSNP153 33..33 33 - - - 103457 RMVar_ID_103457 Human_SNP_ID_76096797 m1A Human chr2 + 67397466 67397466 67397466 GGCGGGCCATAGGCAATGAGTCGGCGAAGGAAACATGATGACAGCCCTAGCCCGAAGAAAACGCC GGCGGGCCATAGGCAATGAGTCGGCGAAGGAACCATGATGACAGCCCTAGCCCGAAGAAAACGCC A C ETAA1 Ensembl:ENSG00000143971 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:67397367..67397618 26863196 MeRIP-seq:(Medium) rs1187621483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918086,Human_RBP_ID_9383941,Human_RBP_ID_18421808,Human_RBP_ID_18764291,Human_RBP_ID_26340959,Human_RBP_ID_27817198 103458 RMVar_ID_103458 Human_SNP_ID_76272305 m1A Human chr2 - 68047317 68047317 68047317 TATGAATTCAAAGAATTTAATTTTTTCCAGTCAGCCATAATGGCAGGTGAAGAAATTAATGAAGA TATGAATTCAAAGAATTTAATTTTTTCCAGTCGGCCATAATGGCAGGTGAAGAAATTAATGAAGA T C C1D Ensembl:ENSG00000197223 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68047291..68047363 26863196 MeRIP-seq:(Medium) rs368582377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623354,Human_RBP_ID_9330486 Human_Splice_Rec_254972,Human_Splice_Rec_254982,Human_Splice_Rec_254990,Human_Splice_Rec_255012,Human_Splice_Rec_255018 RMVar_hsa_circ_285359 103459 RMVar_ID_103459 Human_SNP_ID_76272999 m1A Human chr2 - 68050426 68050425 68050426 AAAGTAAGGTATGTTTGTAGGAGATTTGAGAAAGGATGGAAGGAAAGGAATTAGAGACTGTTAGT AAAGTAAGGTATGTTTGTAGGAGATTTGAGAA_GGATGGAAGGAAAGGAATTAGAGACTGTTAGT CT C C1D Ensembl:ENSG00000197223 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68050424..68050632 26863196 MeRIP-seq:(Medium) rs1236182623 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6942101 103460 RMVar_ID_103460 Human_SNP_ID_76273000 m1A Human chr2 - 68050426 68050426 68050426 AAAGTAAGGTATGTTTGTAGGAGATTTGAGAAAGGATGGAAGGAAAGGAATTAGAGACTGTTAGT AAAGTAAGGTATGTTTGTAGGAGATTTGAGAAGGGATGGAAGGAAAGGAATTAGAGACTGTTAGT T C C1D Ensembl:ENSG00000197223 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68050424..68050632 26863196 MeRIP-seq:(Medium) rs1031718896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6942101 103461 RMVar_ID_103461 Human_SNP_ID_76275992 m1A Human chr2 + 68062896 68062896 68062896 GTCTGCCCAGAGGATGACAGGGGAATCCCAGGAGAGGAAAAGCGGAGTTAAACAGGAGCAGGAGA GTCTGCCCAGAGGATGACAGGGGAATCCCAGGGGAGGAAAAGCGGAGTTAAACAGGAGCAGGAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68062892..68062974 26863196 MeRIP-seq:(Medium) rs1375370318 Functional Loss SNV dbSNP153 33..33 33 - - - 103462 RMVar_ID_103462 Human_SNP_ID_76298943 m1A Human chr2 + 68157442 68157442 68157442 GGGCGATGATCTGAGGCTTCTCGAAGGCCGACATGGTGCAGCCAATTTCAGCTACGGCAACCGCC GGGCGATGATCTGAGGCTTCTCGAAGGCCGACGTGGTGCAGCCAATTTCAGCTACGGCAACCGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:68157363..68157470 26863196 MeRIP-seq:(Medium) rs914143860 Functional Loss SNV dbSNP153 33..33 33 - - - 103463 RMVar_ID_103463 Human_SNP_ID_76298944 m1A Human chr2 + 68157442 68157442 68157442 GGGCGATGATCTGAGGCTTCTCGAAGGCCGACATGGTGCAGCCAATTTCAGCTACGGCAACCGCC GGGCGATGATCTGAGGCTTCTCGAAGGCCGACTTGGTGCAGCCAATTTCAGCTACGGCAACCGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:68157363..68157470 26863196 MeRIP-seq:(Medium) rs914143860 Functional Loss SNV dbSNP153 33..33 33 - - - 103464 RMVar_ID_103464 Human_SNP_ID_76298958 m1A Human chr2 + 68157468 68157468 68157468 GCCGACATGGTGCAGCCAATTTCAGCTACGGCAACCGCCACACCCAGAGCCCCCAAAAACGGCAA GCCGACATGGTGCAGCCAATTTCAGCTACGGCTACCGCCACACCCAGAGCCCCCAAAAACGGCAA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:68157366..68157485 26863196 MeRIP-seq:(Medium) rs778033672 Functional Loss SNV dbSNP153 33..33 33 - - - 103465 RMVar_ID_103465 Human_SNP_ID_76298959 m1A Human chr2 + 68157469 68157469 68157469 CCGACATGGTGCAGCCAATTTCAGCTACGGCAACCGCCACACCCAGAGCCCCCAAAAACGGCAAC CCGACATGGTGCAGCCAATTTCAGCTACGGCACCCGCCACACCCAGAGCCCCCAAAAACGGCAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68157294..68157504 26863196 MeRIP-seq:(Medium) rs1232433404 Functional Loss SNV dbSNP153 33..33 33 - - - 103466 RMVar_ID_103466 Human_SNP_ID_76299368 m1A Human chr2 + 68158062 68158062 68158062 TGAACAGCTGTCCGCAGCAGGAGAGGGCGGGGATGCGGGCCGCATGGACACAGAGGAGGCCAGGC TGAACAGCTGTCCGCAGCAGGAGAGGGCGGGGCTGCGGGCCGCATGGACACAGAGGAGGCCAGGC A C PNO1 Ensembl:ENSG00000115946 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:68157892..68158125;chr2:68157892..68158150;chr2:68157876..68158158 26863196 MeRIP-seq:(Medium) rs1198562232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776859,Human_RBP_ID_5322088,Human_RBP_ID_6942261,Human_RBP_ID_9383945,Human_RBP_ID_22451328,Human_RBP_ID_26339390,Human_RBP_ID_27817199 Human_Splice_Rec_255109,Human_Splice_Rec_255121 103467 RMVar_ID_103467 Human_SNP_ID_76323818 m1A Human chr2 - 68246620 68246620 68246620 ATGATGCCAGATTGAAGGGAGTCTTAAAGAGGAAGGAGTCAGCAGTGAATAGATACTGCAGAGAT ATGATGCCAGATTGAAGGGAGTCTTAAAGAGGGAGGAGTCAGCAGTGAATAGATACTGCAGAGAT T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:68246618..68246802 26863196 MeRIP-seq:(Medium) rs1269250604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9994570 103468 RMVar_ID_103468 Human_SNP_ID_76323829 m1A Human chr2 - 68246644 68246644 68246644 TAGTTGGGAAATGAGCAGCATAGCATGATGCCAGATTGAAGGGAGTCTTAAAGAGGAAGGAGTCA TAGTTGGGAAATGAGCAGCATAGCATGATGCCGGATTGAAGGGAGTCTTAAAGAGGAAGGAGTCA T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68246643..68246784 26863196 MeRIP-seq:(Medium) rs1339036768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13945632 103469 RMVar_ID_103469 Human_SNP_ID_76325481 m1A Human chr2 + 68252217 68252217 68252217 GGCTGGCTCGCAGGAAACGGCGGCGGCGGCCCAGCTGCGGCCCTCGGGTCGCCGGCGGGGAGGGG GGCTGGCTCGCAGGAAACGGCGGCGGCGGCCCGGCTGCGGCCCTCGGGTCGCCGGCGGGGAGGGG A G lnc-PLEK-3,lnc-PLEK-3:2 RNACentral:URS0000D5A60A,RNACentral:URS0000D5B052 lincRNA,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:68252134..68252521 26863196 MeRIP-seq:(Medium) rs1182204904 Functional Loss SNV dbSNP153 33..33 33 - - - 103470 RMVar_ID_103470 Human_SNP_ID_76325540 m1A Human chr2 + 68252341 68252337 68252342 CGCGAGGGAGCGGGCAGGGTAGGGGGAAATAAATTAAGGTCGAGATTCAGAGCCGGAGAGCGCGG CGCGAGGGAGCGGGCAGGGTAGGGGGAAA_____TAAGGTCGAGATTCAGAGCCGGAGAGCGCGG ATAAAT A lnc-PLEK-3,lnc-PLEK-3:2 RNACentral:URS0000D5A60A,RNACentral:URS0000D5B052 lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:68252223..68252423 26863196 MeRIP-seq:(Medium) rs570247131 Functional Loss DEL dbSNP153 30..34 33 - - - 103471 RMVar_ID_103471 Human_SNP_ID_76325542 m1A Human chr2 + 68252341 68252341 68252341 CGCGAGGGAGCGGGCAGGGTAGGGGGAAATAAATTAAGGTCGAGATTCAGAGCCGGAGAGCGCGG CGCGAGGGAGCGGGCAGGGTAGGGGGAAATAAGTTAAGGTCGAGATTCAGAGCCGGAGAGCGCGG A G lnc-PLEK-3,lnc-PLEK-3:2 RNACentral:URS0000D5A60A,RNACentral:URS0000D5B052 lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:68252223..68252423 26863196 MeRIP-seq:(Medium) rs1320764565 Functional Loss SNV dbSNP153 33..33 33 - - - 103472 RMVar_ID_103472 Human_SNP_ID_76325829 m1A Human chr2 + 68252905 68252905 68252905 GCGGGAGGAAGCGCGAGGGGTGCGCGAGTGCTAGCGAAAGGGGGACAGGGGCCCTGGAGTGGAAG GCGGGAGGAAGCGCGAGGGGTGCGCGAGTGCTGGCGAAAGGGGGACAGGGGCCCTGGAGTGGAAG A G AC017083.1 Ensembl:ENSG00000273064 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:68252863..68252966 26863196 MeRIP-seq:(Medium) rs950322076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5322089,Human_RBP_ID_18421810,Human_RBP_ID_26786991 103473 RMVar_ID_103473 Human_SNP_ID_76325839 m1A Human chr2 + 68252917 68252917 68252917 GCGAGGGGTGCGCGAGTGCTAGCGAAAGGGGGACAGGGGCCCTGGAGTGGAAGCCTTGCGGGAGA GCGAGGGGTGCGCGAGTGCTAGCGAAAGGGGGTCAGGGGCCCTGGAGTGGAAGCCTTGCGGGAGA A T AC017083.1 Ensembl:ENSG00000273064 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:68252866..68253017 26863196 MeRIP-seq:(Medium) rs1391990758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5322089,Human_RBP_ID_18421810,Human_RBP_ID_26786991 103474 RMVar_ID_103474 Human_SNP_ID_76335584 m1A Human chr2 - 68293908 68293908 68293908 CTTCTCTGTCATTGAGTATGAATGCAAGCCCAACGAGACACGCAGTCTGATGTGGGTGAACAAGG CTTCTCTGTCATTGAGTATGAATGCAAGCCCAGCGAGACACGCAGTCTGATGTGGGTGAACAAGG T C CNRIP1 Ensembl:ENSG00000119865 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:68293744..68315939 32194978 MeRIP-seq:(Medium) rs148723232 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23881393 Human_miRNA_ID_2141149 RMVar_hsa_circ_79430,RMVar_hsa_circ_200835 103475 RMVar_ID_103475 Human_SNP_ID_76342281 m1A Human chr2 - 68319402 68319402 68319402 CCCCGGAGCCGCCGCGCCAGACCCTCGCCCAGACATGGGGGACCTGCCGGGCCTCGTGCGCCTCT CCCCGGAGCCGCCGCGCCAGACCCTCGCCCAGGCATGGGGGACCTGCCGGGCCTCGTGCGCCTCT T C CNRIP1 Ensembl:ENSG00000119865 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:68319301..68319501 26863410 MeRIP-seq:(Medium) rs1280994730 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_255176 103476 RMVar_ID_103476 Human_SNP_ID_76342282 m1A Human chr2 - 68319402 68319402 68319402 CCCCGGAGCCGCCGCGCCAGACCCTCGCCCAGACATGGGGGACCTGCCGGGCCTCGTGCGCCTCT CCCCGGAGCCGCCGCGCCAGACCCTCGCCCAGCCATGGGGGACCTGCCGGGCCTCGTGCGCCTCT T G CNRIP1 Ensembl:ENSG00000119865 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:68319301..68319501 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_255176 103477 RMVar_ID_103477 Human_SNP_ID_76382545 m1A Human chr2 - 68466407 68466407 68466407 AGCCACCACAGCTAATCTGGATCATGAATGGGAGCCACCGTGGTCTTGGCAAGTCCGAAAACATA AGCCACCACAGCTAATCTGGATCATGAATGGGTGCCACCGTGGTCTTGGCAAGTCCGAAAACATA T A FBXO48 Ensembl:ENSG00000204923 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:68466331..68466472 26863196 MeRIP-seq:(Medium) rs917873606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554183 Human_Splice_Rec_255208 103478 RMVar_ID_103478 Human_SNP_ID_76519053 m1A Human chr2 - 69023283 69023283 69023283 TCACCATCATCTTTATCATCACGTCCACCTCCACCACCATAACCATCACCATCACCATCTATCGT TCACCATCATCTTTATCATCACGTCCACCTCCCCCACCATAACCATCACCATCACCATCTATCGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69023281..69023582 26863196 MeRIP-seq:(Medium) rs200773099 Functional Loss SNV dbSNP153 33..33 33 - - - 103479 RMVar_ID_103479 Human_SNP_ID_76554605 m1A Human chr2 + 69181872 69181872 69181872 TATTATGGTGGGAGAGGCGTTGGAGGCATTAAAAGAATGGAGGTAAGAGGACAGCTTCATATACA TATTATGGTGGGAGAGGCGTTGGAGGCATTAAGAGAATGGAGGTAAGAGGACAGCTTCATATACA A G ANTXR1 Ensembl:ENSG00000169604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:69181776..69181912;chr2:69181776..69181900 26863196 MeRIP-seq:(Medium) rs1303272574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18999597 Human_Splice_Rec_255592,Human_Splice_Rec_255593 RMVar_hsa_circ_14788,RMVar_hsa_circ_376828,RMVar_hsa_circ_20066,RMVar_hsa_circ_46173,RMVar_hsa_circ_309555 103480 RMVar_ID_103480 Human_SNP_ID_76557415 m1A Human chr2 - 69193376 69193376 69193376 CCTGGCTGTGGACGCATCACAGACACACGATCATATCCTTTCCTCAGTAGGACCCACAAGGCATC CCTGGCTGTGGACGCATCACAGACACACGATCGTATCCTTTCCTCAGTAGGACCCACAAGGCATC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:69193256..69193464 26863196 MeRIP-seq:(Medium) rs769362984 Functional Loss SNV dbSNP153 33..33 33 - - - 103481 RMVar_ID_103481 Human_SNP_ID_76559257 m1A Human chr2 + 69201309 69201309 69201309 GTTGGGGAGGTAGAATATTCTAGTGACAGGGAAGCTTGCATACAGATCTGCAGGTGAGACTGTGG GTTGGGGAGGTAGAATATTCTAGTGACAGGGAGGCTTGCATACAGATCTGCAGGTGAGACTGTGG A G ANTXR1 Ensembl:ENSG00000169604 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69201305..69201451 26863196 MeRIP-seq:(Medium) rs971857765 Functional Loss SNV dbSNP153 33..33 33 - - - 103482 RMVar_ID_103482 Human_SNP_ID_76559321 m1A Human chr2 + 69201573 69201573 69201573 TTTAGAAAGGTCGCACTGGCTGCAGTGTGGACATAGCGGCAGTGAGAGAGGCTGGCACCCTGAAG TTTAGAAAGGTCGCACTGGCTGCAGTGTGGACGTAGCGGCAGTGAGAGAGGCTGGCACCCTGAAG A G ANTXR1 Ensembl:ENSG00000169604 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69201568..69201773 26863196 MeRIP-seq:(Medium) rs769422567 Functional Loss SNV dbSNP153 33..33 33 - - - 103483 RMVar_ID_103483 Human_SNP_ID_76559450 m1A Human chr2 + 69202141 69202141 69202141 AGGGGAAACCAGGGAGAGGGGTAGAGAGAAGAAGTTAAGCACTGAACCCTGAGGGTCACATCCTT AGGGGAAACCAGGGAGAGGGGTAGAGAGAAGATGTTAAGCACTGAACCCTGAGGGTCACATCCTT A T ANTXR1 Ensembl:ENSG00000169604 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:69202137..69202447 26863196 MeRIP-seq:(Medium) rs1014929079 Functional Loss SNV dbSNP153 33..33 33 - - - 103484 RMVar_ID_103484 Human_SNP_ID_76559452 m1A Human chr2 - 69202151 69202151 69202151 CCCTGACTTAAAGGATGTGACCCTCAGGGTTCAGTGCTTAACTTCTTCTCTCTACCCCTCTCCCT CCCTGACTTAAAGGATGTGACCCTCAGGGTTCTGTGCTTAACTTCTTCTCTCTACCCCTCTCCCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:69202139..69202264 26863196 MeRIP-seq:(Medium) rs1176518270 Functional Loss SNV dbSNP153 33..33 33 - - - 103485 RMVar_ID_103485 Human_SNP_ID_76559453 m1A Human chr2 - 69202151 69202151 69202151 CCCTGACTTAAAGGATGTGACCCTCAGGGTTCAGTGCTTAACTTCTTCTCTCTACCCCTCTCCCT CCCTGACTTAAAGGATGTGACCCTCAGGGTTCGGTGCTTAACTTCTTCTCTCTACCCCTCTCCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:69202139..69202264 26863196 MeRIP-seq:(Medium) rs1176518270 Functional Loss SNV dbSNP153 33..33 33 - - - 103486 RMVar_ID_103486 Human_SNP_ID_76561676 m1A Human chr2 + 69212232 69212232 69212232 AAAGAAGTAGGGGAGGGGAGGAGGAGGATGGGAGGAGTAGAGAAAGAGAGGAGAAAACCAGGGAG AAAGAAGTAGGGGAGGGGAGGAGGAGGATGGGCGGAGTAGAGAAAGAGAGGAGAAAACCAGGGAG A C ANTXR1 Ensembl:ENSG00000169604 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69212229..69212363 26863196 MeRIP-seq:(Medium) rs775486834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2659890 103487 RMVar_ID_103487 Human_SNP_ID_76564865 m1A Human chr2 + 69226415 69226415 69226415 AAAGACCAGTCAATTGGGGAAGGATGTGGAGCAGGTCATGAGGCCGGAGGAAGGCAAAGGTCAAG AAAGACCAGTCAATTGGGGAAGGATGTGGAGCTGGTCATGAGGCCGGAGGAAGGCAAAGGTCAAG A T ANTXR1 Ensembl:ENSG00000169604 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69226410..69226551 26863196 MeRIP-seq:(Medium) rs1386320878 Functional Loss SNV dbSNP153 33..33 33 - - - 103488 RMVar_ID_103488 Human_SNP_ID_76569163 m1A Human chr2 + 69245335 69245335 69245335 TCGCCGCCTCCTGCCCCCATCTACACTCCCCCACCTCCTGCGCCCCACTGCCCTCCCCCGCCCCC TCGCCGCCTCCTGCCCCCATCTACACTCCCCCCCCTCCTGCGCCCCACTGCCCTCCCCCGCCCCC A C ANTXR1 Ensembl:ENSG00000169604 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:69245287..69245548 26863196 MeRIP-seq:(Medium) rs1161263218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18947922,Human_RBP_ID_27481335 Human_miRNA_ID_1012796,Human_miRNA_ID_1020962,Human_miRNA_ID_1294804,Human_miRNA_ID_1298766,Human_miRNA_ID_1704238 103489 RMVar_ID_103489 Human_SNP_ID_76569164 m1A Human chr2 + 69245335 69245335 69245335 TCGCCGCCTCCTGCCCCCATCTACACTCCCCCACCTCCTGCGCCCCACTGCCCTCCCCCGCCCCC TCGCCGCCTCCTGCCCCCATCTACACTCCCCCGCCTCCTGCGCCCCACTGCCCTCCCCCGCCCCC A G ANTXR1 Ensembl:ENSG00000169604 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:69245287..69245548 26863196 MeRIP-seq:(Medium) rs1161263218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18947922,Human_RBP_ID_27481335 Human_miRNA_ID_1012796,Human_miRNA_ID_1020962,Human_miRNA_ID_1294804,Human_miRNA_ID_1298766,Human_miRNA_ID_1704238 103490 RMVar_ID_103490 Human_SNP_ID_76569229 m1A Human chr2 - 69245410 69245410 69245410 CTGTTGGGAGGTGGAGCCTGGGGAGGAGGGGGAAGGGTGGAAGGTGGGGACGGGATGGGAGGGGT CTGTTGGGAGGTGGAGCCTGGGGAGGAGGGGGTAGGGTGGAAGGTGGGGACGGGATGGGAGGGGT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:69245301..69245525 26863196 MeRIP-seq:(Medium) rs372701153 Functional Loss SNV dbSNP153 33..33 33 - - - 103491 RMVar_ID_103491 Human_SNP_ID_76569230 m1A Human chr2 - 69245410 69245410 69245410 CTGTTGGGAGGTGGAGCCTGGGGAGGAGGGGGAAGGGTGGAAGGTGGGGACGGGATGGGAGGGGT CTGTTGGGAGGTGGAGCCTGGGGAGGAGGGGGGAGGGTGGAAGGTGGGGACGGGATGGGAGGGGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:69245301..69245525 26863196 MeRIP-seq:(Medium) rs372701153 Functional Loss SNV dbSNP153 33..33 33 - - - 103492 RMVar_ID_103492 Human_SNP_ID_76587332 m1A Human chr2 + 69322864 69322864 69322864 CCCCCAAACATGGACCATTATTCAAGTAGACAAAATCACTCACTGACAGCACTTTAACAACCCGC CCCCCAAACATGGACCATTATTCAAGTAGACACAATCACTCACTGACAGCACTTTAACAACCCGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:69322813..69322996 26863196 MeRIP-seq:(Medium) rs1049014918 Functional Loss SNV dbSNP153 33..33 33 - - - 103493 RMVar_ID_103493 Human_SNP_ID_76587333 m1A Human chr2 + 69322864 69322864 69322864 CCCCCAAACATGGACCATTATTCAAGTAGACAAAATCACTCACTGACAGCACTTTAACAACCCGC CCCCCAAACATGGACCATTATTCAAGTAGACAGAATCACTCACTGACAGCACTTTAACAACCCGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:69322813..69322996 26863196 MeRIP-seq:(Medium) rs1049014918 Functional Loss SNV dbSNP153 33..33 33 - - - 103494 RMVar_ID_103494 Human_SNP_ID_76603526 m1A Human chr2 - 69387108 69387108 69387108 AGCTCGTGTGTGCACCCCCGATCCCGCCAGCCACTCGCCCCTGGCCTCGCGGGCCGTGTCTCCGG AGCTCGTGTGTGCACCCCCGATCCCGCCAGCCTCTCGCCCCTGGCCTCGCGGGCCGTGTCTCCGG T A GFPT1 Ensembl:ENSG00000198380 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:69387060..69387200 26863196 MeRIP-seq:(Medium) rs1254271832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_829197,Human_RBP_ID_921525,Human_RBP_ID_4634102,Human_RBP_ID_8851920,Human_RBP_ID_9259786,Human_RBP_ID_9296587,Human_RBP_ID_22765429 Human_Splice_Rec_255687,Human_Splice_Rec_255725,Human_Splice_Rec_255761,Human_Splice_Rec_255795,Human_Splice_Rec_255827 RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 103495 RMVar_ID_103495 Human_SNP_ID_76603538 m1A Human chr2 - 69387127 69387127 69387127 CCCGCAGATTGCCCACCGAAGCTCGTGTGTGCACCCCCGATCCCGCCAGCCACTCGCCCCTGGCC CCCGCAGATTGCCCACCGAAGCTCGTGTGTGCCCCCCCGATCCCGCCAGCCACTCGCCCCTGGCC T G GFPT1 Ensembl:ENSG00000198380 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:69387076..69387208 26863196 MeRIP-seq:(Medium) rs956544079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60515,Human_RBP_ID_829197,Human_RBP_ID_921525,Human_RBP_ID_4625435,Human_RBP_ID_8851920,Human_RBP_ID_9259787,Human_RBP_ID_9296587 Human_Splice_Rec_255687,Human_Splice_Rec_255725,Human_Splice_Rec_255761,Human_Splice_Rec_255795,Human_Splice_Rec_255827 RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 103496 RMVar_ID_103496 Human_SNP_ID_76616812 m1A Human chr2 - 69437393 69437393 69437393 AAGATGGCGGCGACGGCCAGGCGGGGCTGGGGAGCTGCGGCTGTTGCCGCCGGGCTGCGCAGGCG AAGATGGCGGCGACGGCCAGGCGGGGCTGGGGCGCTGCGGCTGTTGCCGCCGGGCTGCGCAGGCG T G NFU1 Ensembl:ENSG00000169599 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69437289..69437396 26863196 MeRIP-seq:(Medium) rs1034660922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243903,Human_RBP_ID_4623365,Human_RBP_ID_9330491,Human_RBP_ID_17392681 Human_Splice_Rec_255847,Human_Splice_Rec_255887,Human_Splice_Rec_255901,Human_Splice_Rec_255921,Human_Splice_Rec_255933 103497 RMVar_ID_103497 Human_SNP_ID_76616824 m1A Human chr2 - 69437407 69437407 69437407 AGGCACTCCGGACTAAGATGGCGGCGACGGCCAGGCGGGGCTGGGGAGCTGCGGCTGTTGCCGCC AGGCACTCCGGACTAAGATGGCGGCGACGGCCTGGCGGGGCTGGGGAGCTGCGGCTGTTGCCGCC T A NFU1 Ensembl:ENSG00000169599 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:69437320..69437407;chr2:69437306..69437627 26863196 MeRIP-seq:(Medium) rs761475695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243903,Human_RBP_ID_4623365,Human_RBP_ID_9330491,Human_RBP_ID_17392681 Human_Splice_Rec_255847,Human_Splice_Rec_255887,Human_Splice_Rec_255901,Human_Splice_Rec_255921,Human_Splice_Rec_255933 103498 RMVar_ID_103498 Human_SNP_ID_76616831 m1A Human chr2 - 69437413 69437413 69437413 ACCCTTAGGCACTCCGGACTAAGATGGCGGCGACGGCCAGGCGGGGCTGGGGAGCTGCGGCTGTT ACCCTTAGGCACTCCGGACTAAGATGGCGGCGGCGGCCAGGCGGGGCTGGGGAGCTGCGGCTGTT T C NFU1 Ensembl:ENSG00000169599 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:69437252..69437418 26863196 MeRIP-seq:(Medium) rs1312689501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243903,Human_RBP_ID_4623365,Human_RBP_ID_9330491,Human_RBP_ID_17392681 Human_Splice_Rec_255847,Human_Splice_Rec_255887,Human_Splice_Rec_255901,Human_Splice_Rec_255921,Human_Splice_Rec_255933 103499 RMVar_ID_103499 Human_SNP_ID_76632010 m1A Human chr2 - 69499319 69499319 69499319 GTTGGGGGTCCTAGAAGAAGGTTGAAGGTCCAAGAAGTTGAGTGTTGGAAGGTGTGAGATTAGGA GTTGGGGGTCCTAGAAGAAGGTTGAAGGTCCAGGAAGTTGAGTGTTGGAAGGTGTGAGATTAGGA T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:69499147..69499342 26863196 MeRIP-seq:(Medium) rs1281833524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200930,RMVar_hsa_circ_110927,RMVar_hsa_circ_200935,RMVar_hsa_circ_81604,RMVar_hsa_circ_200937,RMVar_hsa_circ_107364,RMVar_hsa_circ_200939,RMVar_hsa_circ_200940 103500 RMVar_ID_103500 Human_SNP_ID_76659955 m1A Human chr2 - 69618780 69618774 69618780 GGATGTGTAGGTCATTGAGAGGACCAAAGGTCAGTGTCGTGAAGAAATCTGGAGGCTGCAGTTTA GGATGTGTAGGTCATTGAGAGGACCAAAGGTC______GTGAAGAAATCTGGAGGCTGCAGTTTA CGACACT C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:69618778..69618926 26863196 MeRIP-seq:(Medium) rs1243832941 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_107364,RMVar_hsa_circ_200940,RMVar_hsa_circ_65166,RMVar_hsa_circ_200951,RMVar_hsa_circ_126250 103501 RMVar_ID_103501 Human_SNP_ID_76665777 m1A Human chr2 - 69642824 69642824 69642824 CGTAAATTAAAATCTTGTGCTGATGCGGCAATACTGTGGTTTCTAGTTGTTGCATGTATGAATGG CGTAAATTAAAATCTTGTGCTGATGCGGCAATTCTGTGGTTTCTAGTTGTTGCATGTATGAATGG T A AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69642818..69642903 26863196 MeRIP-seq:(Medium) rs891344411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2660301,Human_RBP_ID_3632505 RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_107364,RMVar_hsa_circ_200940,RMVar_hsa_circ_65166,RMVar_hsa_circ_200951,RMVar_hsa_circ_126250 103502 RMVar_ID_103502 Human_SNP_ID_76665778 m1A Human chr2 - 69642824 69642824 69642824 CGTAAATTAAAATCTTGTGCTGATGCGGCAATACTGTGGTTTCTAGTTGTTGCATGTATGAATGG CGTAAATTAAAATCTTGTGCTGATGCGGCAATGCTGTGGTTTCTAGTTGTTGCATGTATGAATGG T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69642818..69642903 26863196 MeRIP-seq:(Medium) rs891344411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2660301,Human_RBP_ID_3632505 RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_107364,RMVar_hsa_circ_200940,RMVar_hsa_circ_65166,RMVar_hsa_circ_200951,RMVar_hsa_circ_126250 103503 RMVar_ID_103503 Human_SNP_ID_76705423 m1A Human chr2 + 69811105 69811105 69811105 AAATTTGGTTGTAGAAACAAAGAAAAGCCTTCATGACAGAGATGCTGGTTCAGAGAGGACTTGGA AAATTTGGTTGTAGAAACAAAGAAAAGCCTTCGTGACAGAGATGCTGGTTCAGAGAGGACTTGGA A G ANXA4 Ensembl:ENSG00000196975 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:69811100..69811318 26863196 MeRIP-seq:(Medium) rs1386347826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200960,RMVar_hsa_circ_278152,RMVar_hsa_circ_367856,RMVar_hsa_circ_200961,RMVar_hsa_circ_48288,RMVar_hsa_circ_313584,RMVar_hsa_circ_200963,RMVar_hsa_circ_66273,RMVar_hsa_circ_61379,RMVar_hsa_circ_74940,RMVar_hsa_circ_357771 103504 RMVar_ID_103504 Human_SNP_ID_76725542 m1A Human chr2 - 69895078 69895078 69895078 CCGGGAACGCCTACGTTCTAATGCAAACGCACACAAATTGCAGAACTGATAATTACCTCAAATAT CCGGGAACGCCTACGTTCTAATGCAAACGCACGCAAATTGCAGAACTGATAATTACCTCAAATAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:69895076..69895200 32194978 MeRIP-seq:(Medium) rs1446249354 Functional Loss SNV dbSNP153 33..33 33 - - - 103505 RMVar_ID_103505 Human_SNP_ID_76725941 m1A Human chr2 - 69896550 69896550 69896550 ACTTTTCCTACAGTTATTTATCTAATAACATTACCAGTAATCTGCCGTTCTTTGCTCTTTGTTTC ACTTTTCCTACAGTTATTTATCTAATAACATTGCCAGTAATCTGCCGTTCTTTGCTCTTTGTTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr2:69896505..69896592;chr2:69896501..69896550 26863196,32194978 MeRIP-seq:(Medium) rs1221215421 Functional Loss SNV dbSNP153 33..33 33 - - - 103506 RMVar_ID_103506 Human_SNP_ID_76748165 m1A Human chr2 - 69985340 69985340 69985340 TCATGAAACAAGGGAAGGACTTCGCATGAACCAGTGGCGATCAGGTGCCAGGAAATGAGGAGTGT TCATGAAACAAGGGAAGGACTTCGCATGAACCGGTGGCGATCAGGTGCCAGGAAATGAGGAGTGT T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69985212..69985359 26863196 MeRIP-seq:(Medium) rs1364852170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3641893 RMVar_hsa_circ_3412 103507 RMVar_ID_103507 Human_SNP_ID_76751901 m1A Human chr2 - 69999866 69999866 69999866 GGAGGAAGGAGGAGGAGCCCGGGGTGACTCACAGGTGCTGACCCGGAGGAGGGCAGGGTGTGAGC GGAGGAAGGAGGAGGAGCCCGGGGTGACTCACGGGTGCTGACCCGGAGGAGGGCAGGGTGTGAGC T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69999817..70000047 26863196 MeRIP-seq:(Medium) rs1019276783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_37272,RMVar_hsa_circ_200983,RMVar_hsa_circ_273703,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_296518,RMVar_hsa_circ_200985,RMVar_hsa_circ_200986 103508 RMVar_ID_103508 Human_SNP_ID_76777535 m1A Human chr2 - 70087616 70087606 70087616 CCGGCGCGAGGCGAGCGAGGGCCGCGGGAGCGAGCGGGAGCGGGCGGGAGGCCGCAGCGTAGTCG CCGGCGCGAGGCGAGCGAGGGCCGCGGGAGCG__________GGCGGGAGGCCGCAGCGTAGTCG CCGCTCCCGCT C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:70087476..70087804 26863196 MeRIP-seq:(Medium) rs1256835290 Functional Loss DEL dbSNP153 33..42 33 - - - 103509 RMVar_ID_103509 Human_SNP_ID_76777542 m1A Human chr2 - 70087616 70087616 70087616 CCGGCGCGAGGCGAGCGAGGGCCGCGGGAGCGAGCGGGAGCGGGCGGGAGGCCGCAGCGTAGTCG CCGGCGCGAGGCGAGCGAGGGCCGCGGGAGCGGGCGGGAGCGGGCGGGAGGCCGCAGCGTAGTCG T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:70087476..70087804 26863196 MeRIP-seq:(Medium) rs1197505973 Functional Loss SNV dbSNP153 33..33 33 - - - 103510 RMVar_ID_103510 Human_SNP_ID_76777561 m1A Human chr2 - 70087672 70087672 70087672 ACGTGGTCAAGTCTTTGGCGGCTGGCGGGGGGAGGGGAGGTGTAGGCCCAAAACTGCCGGCGCGA ACGTGGTCAAGTCTTTGGCGGCTGGCGGGGGGGGGGGAGGTGTAGGCCCAAAACTGCCGGCGCGA T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:70087451..70088673;chr2:70087476..70087775;chr2:70087476..70087795;chr2:70087476..70087800 26863196 MeRIP-seq:(Medium) rs1250216469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3642344,Human_RBP_ID_8203309 103511 RMVar_ID_103511 Human_SNP_ID_76777576 m1A Human chr2 - 70087696 70087696 70087696 GCGTTCGGGGGAGTTGGGCTCGTTACGTGGTCAAGTCTTTGGCGGCTGGCGGGGGGAGGGGAGGT GCGTTCGGGGGAGTTGGGCTCGTTACGTGGTCCAGTCTTTGGCGGCTGGCGGGGGGAGGGGAGGT T G PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:70087526..70088474;chr2:70087526..70088510 26863196 MeRIP-seq:(Medium) rs1356230484 Functional Loss SNV dbSNP153 33..33 33 - - - 103512 RMVar_ID_103512 Human_SNP_ID_76777604 m1A Human chr2 + 70087724 70087724 70087724 GACTTGACCACGTAACGAGCCCAACTCCCCCGAACGCCGCCCGCCGCTCGCCATGGATGCCGGTG GACTTGACCACGTAACGAGCCCAACTCCCCCGGACGCCGCCCGCCGCTCGCCATGGATGCCGGTG A G PCBP1 Ensembl:ENSG00000169564 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr2:70087526..70088616;chr2:70087476..70087787 26863196 MeRIP-seq:(Medium) rs1215135867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554573,Human_RBP_ID_777422,Human_RBP_ID_1922348,Human_RBP_ID_6944372,Human_RBP_ID_9110093,Human_RBP_ID_9330501,Human_RBP_ID_13949288,Human_RBP_ID_17392691,Human_RBP_ID_17509671,Human_RBP_ID_17960401,Human_RBP_ID_18193297,Human_RBP_ID_18764649,Human_RBP_ID_23882222,Human_RBP_ID_27291850 103513 RMVar_ID_103513 Human_SNP_ID_76777832 m1A Human chr2 + 70088378 70088378 70088378 CAGCGACGCTGCGGGCTACCCCCATGCCACCCATGACCTGGAGGGACCACCTCTAGATGCCTACT CAGCGACGCTGCGGGCTACCCCCATGCCACCCTTGACCTGGAGGGACCACCTCTAGATGCCTACT A T PCBP1 Ensembl:ENSG00000169564 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:70087803..70088425 32194978 MeRIP-seq:(Medium) rs776286045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554581,Human_RBP_ID_1589444,Human_RBP_ID_1922358,Human_RBP_ID_3632716,Human_RBP_ID_6944395,Human_RBP_ID_8849556,Human_RBP_ID_17392695,Human_RBP_ID_18193308,Human_RBP_ID_22451345,Human_RBP_ID_26484694,Human_RBP_ID_27483243 103514 RMVar_ID_103514 Human_SNP_ID_76786896 m1A Human chr2 - 70124219 70124219 70124219 CTGCCCGTGCTTCCTCCTAACCACTTCCCCCCAGCGACCGCGGAAGGCGCTTCCTCCCCCGCAGC CTGCCCGTGCTTCCTCCTAACCACTTCCCCCCCGCGACCGCGGAAGGCGCTTCCTCCCCCGCAGC T G LINC01816 Ensembl:ENSG00000231327 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:70124183..70124312 26863196 MeRIP-seq:(Medium) rs1408404771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3189953 103515 RMVar_ID_103515 Human_SNP_ID_76786914 m1A Human chr2 + 70124244 70124244 70124244 CGGTCGCTGGGGGGAAGTGGTTAGGAGGAAGCACGGGCAGTGGAGGGGACTGCTGGAGGGTCCCA CGGTCGCTGGGGGGAAGTGGTTAGGAGGAAGCGCGGGCAGTGGAGGGGACTGCTGGAGGGTCCCA A G lnc-PCBP1-9,lnc-PCBP1-9:2 RNACentral:URS00008BF05C,RNACentral:URS0000D56EEF lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:70124144..70124375 26863196 MeRIP-seq:(Medium) rs763030379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23882256 103516 RMVar_ID_103516 Human_SNP_ID_76786915 m1A Human chr2 + 70124244 70124244 70124244 CGGTCGCTGGGGGGAAGTGGTTAGGAGGAAGCACGGGCAGTGGAGGGGACTGCTGGAGGGTCCCA CGGTCGCTGGGGGGAAGTGGTTAGGAGGAAGCTCGGGCAGTGGAGGGGACTGCTGGAGGGTCCCA A T lnc-PCBP1-9,lnc-PCBP1-9:2 RNACentral:URS00008BF05C,RNACentral:URS0000D56EEF lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:70124144..70124375 26863196 MeRIP-seq:(Medium) rs763030379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23882256 103517 RMVar_ID_103517 Human_SNP_ID_76810900 m1A Human chr2 - 70211180 70211172 70211180 GGAAGTTTCACTTTGTTTTCAGTGAAGATCACAAACCTCCTTCTTCCTTTACTCAAGAGGAAAGG GGAAGTTTCACTTTGTTTTCAGTGAAGATCAC________TTCTTCCTTTACTCAAGAGGAAAGG AGGAGGTTT A TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:70211130..70211240 32194978 MeRIP-seq:(Medium) rs1261759695 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_1023976,Human_RBP_ID_1922381,Human_RBP_ID_8109085,Human_RBP_ID_17017212,Human_RBP_ID_17960440,Human_RBP_ID_18166865 Human_miRNA_ID_116275 RMVar_hsa_circ_95306,RMVar_hsa_circ_201004 103518 RMVar_ID_103518 Human_SNP_ID_76819905 m1A Human chr2 - 70244080 70244080 70244080 TGAAGAGAGTAAATGTAGTAGAGGAGTAGGAAATGAGGTCAGAATGATAAATAGGAATGTTAGGG TGAAGAGAGTAAATGTAGTAGAGGAGTAGGAATTGAGGTCAGAATGATAAATAGGAATGTTAGGG T A TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:70244078..70244164 26863196 MeRIP-seq:(Medium) rs1311942061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13950382,Human_RBP_ID_23882413 RMVar_hsa_circ_201027 103519 RMVar_ID_103519 Human_SNP_ID_76819906 m1A Human chr2 - 70244080 70244080 70244080 TGAAGAGAGTAAATGTAGTAGAGGAGTAGGAAATGAGGTCAGAATGATAAATAGGAATGTTAGGG TGAAGAGAGTAAATGTAGTAGAGGAGTAGGAAGTGAGGTCAGAATGATAAATAGGAATGTTAGGG T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:70244078..70244164 26863196 MeRIP-seq:(Medium) rs1311942061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13950382,Human_RBP_ID_23882413 RMVar_hsa_circ_201027 103520 RMVar_ID_103520 Human_SNP_ID_76821263 m1A Human chr2 - 70248549 70248549 70248549 TTTAGTGTAATTGCCGCCGGAGGAGGAGGCGGAGTAACCTCTGGTCAGCCGAGAAACCCCACTAT TTTAGTGTAATTGCCGCCGGAGGAGGAGGCGGGGTAACCTCTGGTCAGCCGAGAAACCCCACTAT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:70248401..70248668;chr2:70248401..70248669 26863196 MeRIP-seq:(Medium) rs1328821263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242629,Human_RBP_ID_775397,Human_RBP_ID_830696,Human_RBP_ID_915530,Human_RBP_ID_4623375,Human_RBP_ID_8524206,Human_RBP_ID_9330503,Human_RBP_ID_9383974,Human_RBP_ID_13950475,Human_RBP_ID_18421817,Human_RBP_ID_26339400,Human_RBP_ID_27817211 RMVar_hsa_circ_201028,RMVar_hsa_circ_125086 103521 RMVar_ID_103521 Human_SNP_ID_76821270 m1A Human chr2 - 70248561 70248561 70248561 TGGGCCGGGCGGTTTAGTGTAATTGCCGCCGGAGGAGGAGGCGGAGTAACCTCTGGTCAGCCGAG TGGGCCGGGCGGTTTAGTGTAATTGCCGCCGGGGGAGGAGGCGGAGTAACCTCTGGTCAGCCGAG T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:70248498..70248650 26863196 MeRIP-seq:(Medium) rs1368079700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775397,Human_RBP_ID_830696,Human_RBP_ID_915530,Human_RBP_ID_4623375,Human_RBP_ID_9330503,Human_RBP_ID_9383974,Human_RBP_ID_18421818,Human_RBP_ID_26339400,Human_RBP_ID_27817211 RMVar_hsa_circ_201028,RMVar_hsa_circ_125086 103522 RMVar_ID_103522 Human_SNP_ID_76824195 m1A Human chr2 - 70258210 70258210 70258210 CTCGGGGCATCCGCAGCTGCACAGCAACAGCCACAACCCCAGCAGCGAGGAGACGAGCTCCGCGA CTCGGGGCATCCGCAGCTGCACAGCAACAGCCGCAACCCCAGCAGCGAGGAGACGAGCTCCGCGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:70258160..70258419 26863196 MeRIP-seq:(Medium) rs760785610 Functional Loss SNV dbSNP153 33..33 33 - - - 103523 RMVar_ID_103523 Human_SNP_ID_76834176 m1A Human chr2 - 70293679 70293679 70293679 GGAGCGTGAGGAAAGCCGTGCGTTGCGTTCCAAGGCATCTGTGAGCCCGCGGAGTATACACCATG GGAGCGTGAGGAAAGCCGTGCGTTGCGTTCCACGGCATCTGTGAGCCCGCGGAGTATACACCATG T G SNRPG Ensembl:ENSG00000143977 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr2:70293561..70293750;chr2:70293550..70293750;chr2:70293601..70293725 26863196,32194978 MeRIP-seq:(Medium) rs756875894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_146771,Human_RBP_ID_554731,Human_RBP_ID_777149,Human_RBP_ID_1589549,Human_RBP_ID_1922487,Human_RBP_ID_4615017,Human_RBP_ID_5118286,Human_RBP_ID_5146573,Human_RBP_ID_5322093,Human_RBP_ID_8524250,Human_RBP_ID_9110161,Human_RBP_ID_9330504,Human_RBP_ID_18764772,Human_RBP_ID_19097586,Human_RBP_ID_22426386,Human_RBP_ID_22451358,Human_RBP_ID_23882500,Human_RBP_ID_24376464,Human_RBP_ID_27014126,Human_RBP_ID_27564029 Human_Splice_Rec_258837,Human_Splice_Rec_258843,Human_Splice_Rec_258873,Human_Splice_Rec_258881,Human_Splice_Rec_258883 103524 RMVar_ID_103524 Human_SNP_ID_76836601 m1A Human chr2 - 70301942 70301941 70301943 TGGAGTCCATGGTGAAGAGTCTGGAAAGAGAGAACATCCGGAAGATGCAGGTAGCGGGGCTGGGG TGGAGTCCATGGTGAAGAGTCTGGAAAGAGA__ACATCCGGAAGATGCAGGTAGCGGGGCTGGGG TTC T FAM136A Ensembl:ENSG00000035141 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1425737210 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_243373,Human_RBP_ID_1589567,Human_RBP_ID_1922500,Human_RBP_ID_3632882,Human_RBP_ID_4623380,Human_RBP_ID_5322094,Human_RBP_ID_8524260,Human_RBP_ID_9383975,Human_RBP_ID_18470797,Human_RBP_ID_18764778,Human_RBP_ID_19001788,Human_RBP_ID_19100587,Human_RBP_ID_22505863,Human_RBP_ID_26340971 Human_Splice_Rec_258887,Human_Splice_Rec_258891,Human_Splice_Rec_258899,Human_Splice_Rec_258909 103525 RMVar_ID_103525 Human_SNP_ID_76836677 m1A Human chr2 - 70302038 70302038 70302038 CGTACGCCGATTCCATATGGGCGCCGGCGCGGAGCGCCGCGGGGCAGCGCGGGGTCGCCATGGCT CGTACGCCGATTCCATATGGGCGCCGGCGCGGCGCGCCGCGGGGCAGCGCGGGGTCGCCATGGCT T G FAM136A Ensembl:ENSG00000035141 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr2:70301989..70302090 26863410 MeRIP-seq:(Medium) rs1379188695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243373,Human_RBP_ID_4623380,Human_RBP_ID_9331041,Human_RBP_ID_18422746,Human_RBP_ID_22452284 103526 RMVar_ID_103526 Human_SNP_ID_76990218 m1A Human chr2 - 70933145 70933145 70933145 GGCGCTGCCCACTTTCCGTTCTAGCCAGCTGTATGGCTCGAAGGCCGAGGAACCCAGTTCGTAGC GGCGCTGCCCACTTTCCGTTCTAGCCAGCTGTGTGGCTCGAAGGCCGAGGAACCCAGTTCGTAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:70933096..70933197 32194978 MeRIP-seq:(Medium) rs1553414659 Functional Loss SNV dbSNP153 33..33 33 - - - 103527 RMVar_ID_103527 Human_SNP_ID_77004810 m1A Human chr2 - 70988217 70988217 70988217 GTTCTCTGGGCAGGTGGCCATGGGGAGGGGCCATGGCTTGGCATGTCCAACAGAAATAGTTTTTG GTTCTCTGGGCAGGTGGCCATGGGGAGGGGCCGTGGCTTGGCATGTCCAACAGAAATAGTTTTTG T C AC007040.2,TEX261 Ensembl:ENSG00000258881,Ensembl:ENSG00000144043 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:70988166..70988266 32194978 MeRIP-seq:(Medium) rs963374125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242955,Human_RBP_ID_554925,Human_RBP_ID_9110237,Human_RBP_ID_17135745,Human_RBP_ID_17279047,Human_RBP_ID_17391880,Human_RBP_ID_17960611,Human_RBP_ID_26486461 Human_miRNA_ID_940077 RMVar_hsa_circ_111599,RMVar_hsa_circ_128103,RMVar_hsa_circ_113984,RMVar_hsa_circ_201053,RMVar_hsa_circ_94596,RMVar_hsa_circ_102818,RMVar_hsa_circ_201055,RMVar_hsa_circ_92410,RMVar_hsa_circ_201054,RMVar_hsa_circ_201051,RMVar_hsa_circ_201052,RMVar_hsa_circ_201050 103528 RMVar_ID_103528 Human_SNP_ID_77004896 m1A Human chr2 + 70988542 70988542 70988542 TGCCTTCCCGACTTCTGGTCCCCACCTGGCATAGAGGCCCAGGGGCCTGACTCTCCTGATCTTGC TGCCTTCCCGACTTCTGGTCCCCACCTGGCATGGAGGCCCAGGGGCCTGACTCTCCTGATCTTGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:70988364..70988612 32194978 MeRIP-seq:(Medium) rs782302167 Functional Loss SNV dbSNP153 33..33 33 - - - 103529 RMVar_ID_103529 Human_SNP_ID_77006298 m1A Human chr2 + 70993766 70993766 70993766 TGTATTCTTCTATCAGTTCTGCCAGGTAATAGAGTCCAGCCGCTGCAGGGTGGGAGGCAGGGAGA TGTATTCTTCTATCAGTTCTGCCAGGTAATAGTGTCCAGCCGCTGCAGGGTGGGAGGCAGGGAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:70991969..71002564 26863196 MeRIP-seq:(Medium) rs1217495977 Functional Loss SNV dbSNP153 33..33 33 - - - 103530 RMVar_ID_103530 Human_SNP_ID_77027669 m1A Human chr2 + 71068697 71068697 71068697 CAGCGACGGTAGCAGCAGCATGGCCGCGATCTATGGGGGTGTAGAGGGGTGAGTGCGGCCCGGCG CAGCGACGGTAGCAGCAGCATGGCCGCGATCTCTGGGGGTGTAGAGGGGTGAGTGCGGCCCGGCG A C NAGK Ensembl:ENSG00000124357 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:71068601..71068816 26863196 MeRIP-seq:(Medium) rs774813675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_259569,Human_Splice_Rec_259571,Human_Splice_Rec_259589,Human_Splice_Rec_259619,Human_Splice_Rec_259625,Human_Splice_Rec_259641,Human_Splice_Rec_259653,Human_Splice_Rec_259671,Human_Splice_Rec_259673,Human_Splice_Rec_259679,Human_Splice_Rec_259697,Human_Splice_Rec_259715,Human_Splice_Rec_259717,Human_Splice_Rec_259745 103531 RMVar_ID_103531 Human_SNP_ID_77027670 m1A Human chr2 + 71068697 71068697 71068697 CAGCGACGGTAGCAGCAGCATGGCCGCGATCTATGGGGGTGTAGAGGGGTGAGTGCGGCCCGGCG CAGCGACGGTAGCAGCAGCATGGCCGCGATCTGTGGGGGTGTAGAGGGGTGAGTGCGGCCCGGCG A G NAGK Ensembl:ENSG00000124357 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:71068601..71068816 26863196 MeRIP-seq:(Medium) rs774813675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_259569,Human_Splice_Rec_259571,Human_Splice_Rec_259589,Human_Splice_Rec_259619,Human_Splice_Rec_259625,Human_Splice_Rec_259641,Human_Splice_Rec_259653,Human_Splice_Rec_259671,Human_Splice_Rec_259673,Human_Splice_Rec_259679,Human_Splice_Rec_259697,Human_Splice_Rec_259715,Human_Splice_Rec_259717,Human_Splice_Rec_259745 103532 RMVar_ID_103532 Human_SNP_ID_77028136 m1A Human chr2 - 71070525 71070525 71070525 CTGCCAGGATCTTCCCATCCTCTGAGACTAAAAGGACCTCGGATCGTGTGCCTCCCCTACAGAAC CTGCCAGGATCTTCCCATCCTCTGAGACTAAAGGGACCTCGGATCGTGTGCCTCCCCTACAGAAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:71070500..71070629 26863196 MeRIP-seq:(Medium) rs1340093703 Functional Loss SNV dbSNP153 33..33 33 - - - 103533 RMVar_ID_103533 Human_SNP_ID_77028507 m1A Human chr2 + 71071741 71071741 71071741 CCAGGAGGACGCGGGGAGGATCCTGATCGAGGAGCTGAGGGACCGATTTCCCTACCTGAGTGAAA CCAGGAGGACGCGGGGAGGATCCTGATCGAGGGGCTGAGGGACCGATTTCCCTACCTGAGTGAAA A G NAGK Ensembl:ENSG00000124357 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:71071633..71071776 26863196 MeRIP-seq:(Medium) rs763158594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19001791,Human_RBP_ID_22997362 Human_Splice_Rec_259576,Human_Splice_Rec_259577,Human_Splice_Rec_259594,Human_Splice_Rec_259595,Human_Splice_Rec_259620,Human_Splice_Rec_259621,Human_Splice_Rec_259628,Human_Splice_Rec_259629,Human_Splice_Rec_259658,Human_Splice_Rec_259659,Human_Splice_Rec_259684,Human_Splice_Rec_259685,Human_Splice_Rec_259702,Human_Splice_Rec_259703,Human_Splice_Rec_259724,Human_Splice_Rec_259725,Human_Splice_Rec_259742,Human_Splice_Rec_259743,Human_Splice_Rec_259750,Human_Splice_Rec_259751,Human_Splice_Rec_259759,Human_Splice_Rec_259776,Human_Splice_Rec_259777,Human_Splice_Rec_259782,Human_Splice_Rec_259783,Human_Splice_Rec_259793,Human_Splice_Rec_259801 RMVar_hsa_circ_125576,RMVar_hsa_circ_201058 103534 RMVar_ID_103534 Human_SNP_ID_77040498 m1A Human chr2 + 71117965 71117959 71117965 GGGGCTGCCCTCTTCATCCCATCTGAGCTCCCACTCACAATTCCAGGCCACACCACCCCTGCACA GGGGCTGCCCTCTTCATCCCATCTGAG______CTCACAATTCCAGGCCACACCACCCCTGCACA GCTCCCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:71117797..71118405 26863196 MeRIP-seq:(Medium) rs1392399078 Functional Loss DEL dbSNP153 28..33 33 - - - 103535 RMVar_ID_103535 Human_SNP_ID_77044393 m1A Human chr2 + 71133194 71133194 71133194 TGGTTCAGAGATAGAGGCTGATGACAAGGAGGACCTAGAAGATTTAGAGGAGGAGGAAGTGTCCG TGGTTCAGAGATAGAGGCTGATGACAAGGAGGGCCTAGAAGATTTAGAGGAGGAGGAAGTGTCCG A G MPHOSPH10 Ensembl:ENSG00000124383 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:71133144..71133248 26863196 MeRIP-seq:(Medium) rs1441613580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61129,Human_RBP_ID_2660930,Human_RBP_ID_6945324,Human_RBP_ID_8942587,Human_RBP_ID_9383979,Human_RBP_ID_13951894,Human_RBP_ID_22997363,Human_RBP_ID_24545800,Human_RBP_ID_26339406,Human_RBP_ID_27817216 103536 RMVar_ID_103536 Human_SNP_ID_77058143 m1A Human chr2 - 71184996 71184996 71184996 GCCCAGGCTCCTGAACCATCAGGAACCCAGGAATCTACCCAACTGTGAGGAGGGGGCAGGCCTTC GCCCAGGCTCCTGAACCATCAGGAACCCAGGAGTCTACCCAACTGTGAGGAGGGGGCAGGCCTTC T C PAIP2B Ensembl:ENSG00000124374 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs187181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18318812 103537 RMVar_ID_103537 Human_SNP_ID_77093033 m1A Human chr2 + 71331844 71331844 71331844 GGAGGCTGAGTGCTAAACTGTGTGGGGCGCGGATGGGATCCAGCTGTTAGTCGGGTAGGCATAGG GGAGGCTGAGTGCTAAACTGTGTGGGGCGCGGCTGGGATCCAGCTGTTAGTCGGGTAGGCATAGG A C ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:71331822..71331938 26863196 MeRIP-seq:(Medium) rs947730057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281136,Human_RBP_ID_827240,Human_RBP_ID_1922601,Human_RBP_ID_4615467,Human_RBP_ID_5471025,Human_RBP_ID_6945587,Human_RBP_ID_8849636,Human_RBP_ID_9110285,Human_RBP_ID_18421822,Human_RBP_ID_18764913,Human_RBP_ID_22996836,Human_RBP_ID_23882925,Human_RBP_ID_27818615,Human_RBP_ID_27840032 Human_Splice_Rec_259943,Human_Splice_Rec_259945,Human_Splice_Rec_259953,Human_Splice_Rec_259961,Human_Splice_Rec_260015,Human_Splice_Rec_260019,Human_Splice_Rec_260023,Human_Splice_Rec_260027,Human_Splice_Rec_260033,Human_Splice_Rec_260035 RMVar_hsa_circ_88409,RMVar_hsa_circ_201063 103538 RMVar_ID_103538 Human_SNP_ID_77093034 m1A Human chr2 + 71331844 71331844 71331844 GGAGGCTGAGTGCTAAACTGTGTGGGGCGCGGATGGGATCCAGCTGTTAGTCGGGTAGGCATAGG GGAGGCTGAGTGCTAAACTGTGTGGGGCGCGGGTGGGATCCAGCTGTTAGTCGGGTAGGCATAGG A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:71331822..71331938 26863196 MeRIP-seq:(Medium) rs947730057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_281136,Human_RBP_ID_827240,Human_RBP_ID_1922601,Human_RBP_ID_4615467,Human_RBP_ID_5471025,Human_RBP_ID_6945587,Human_RBP_ID_8849636,Human_RBP_ID_9110285,Human_RBP_ID_18421822,Human_RBP_ID_18764913,Human_RBP_ID_22996836,Human_RBP_ID_23882925,Human_RBP_ID_27818615,Human_RBP_ID_27840032 Human_Splice_Rec_259943,Human_Splice_Rec_259945,Human_Splice_Rec_259953,Human_Splice_Rec_259961,Human_Splice_Rec_260015,Human_Splice_Rec_260019,Human_Splice_Rec_260023,Human_Splice_Rec_260027,Human_Splice_Rec_260033,Human_Splice_Rec_260035 RMVar_hsa_circ_88409,RMVar_hsa_circ_201063 103539 RMVar_ID_103539 Human_SNP_ID_77093035 m1A Human chr2 - 71331845 71331845 71331845 ACCTATGCCTACCCGACTAACAGCTGGATCCCATCCGCGCCCCACACAGTTTAGCACTCAGCCTC ACCTATGCCTACCCGACTAACAGCTGGATCCCTTCCGCGCCCCACACAGTTTAGCACTCAGCCTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:71331795..71332008 26863196 MeRIP-seq:(Medium) rs1426775065 Functional Loss SNV dbSNP153 33..33 33 - - - 103540 RMVar_ID_103540 Human_SNP_ID_77107514 m1A Human chr2 + 71382467 71382467 71382467 TTTTTTGAGATCCGCTCAGATTGAAGAGTGACAGGAAGAGTTAATTAGAGCAGTTTTAAGGATAA TTTTTTGAGATCCGCTCAGATTGAAGAGTGACTGGAAGAGTTAATTAGAGCAGTTTTAAGGATAA A T ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:71382417..71382501 26863196 MeRIP-seq:(Medium) rs1250708756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9995986,Human_RBP_ID_13954922,Human_RBP_ID_22995142,Human_RBP_ID_25562973 RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_5314,RMVar_hsa_circ_31128,RMVar_hsa_circ_54993,RMVar_hsa_circ_44254,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_69432,RMVar_hsa_circ_3533,RMVar_hsa_circ_201068,RMVar_hsa_circ_60785,RMVar_hsa_circ_71144,RMVar_hsa_circ_360186,RMVar_hsa_circ_37061,RMVar_hsa_circ_40482,RMVar_hsa_circ_31207,RMVar_hsa_circ_276924,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_340920,RMVar_hsa_circ_302477,RMVar_hsa_circ_326814,RMVar_hsa_circ_276970,RMVar_hsa_circ_3462,RMVar_hsa_circ_59534,RMVar_hsa_circ_59773,RMVar_hsa_circ_52410,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_52069,RMVar_hsa_circ_25874,RMVar_hsa_circ_17646,RMVar_hsa_circ_201081,RMVar_hsa_circ_201082,RMVar_hsa_circ_58214,RMVar_hsa_circ_345331,RMVar_hsa_circ_201085,RMVar_hsa_circ_347897 103541 RMVar_ID_103541 Human_SNP_ID_77119522 m1A Human chr2 + 71423472 71423472 71423472 AAAAGGAGGAGAAGGAATTTAATACTAAGGAAACCAGAATGGATCTTCAAATAGGAACAGAGAAG AAAAGGAGGAGAAGGAATTTAATACTAAGGAATCCAGAATGGATCTTCAAATAGGAACAGAGAAG A T ZNF638 Ensembl:ENSG00000075292 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:71423423..71423522 26863196 MeRIP-seq:(Medium) rs761918477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_56466,Human_RBP_ID_2661710,Human_RBP_ID_8524671,Human_RBP_ID_18533711,Human_RBP_ID_18765150,Human_RBP_ID_24545805,Human_RBP_ID_26339428 RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_3533,RMVar_hsa_circ_40482,RMVar_hsa_circ_11732,RMVar_hsa_circ_74582,RMVar_hsa_circ_201092,RMVar_hsa_circ_201098,RMVar_hsa_circ_71350,RMVar_hsa_circ_314084,RMVar_hsa_circ_350139,RMVar_hsa_circ_329327,RMVar_hsa_circ_201100,RMVar_hsa_circ_299668,RMVar_hsa_circ_201099,RMVar_hsa_circ_201101,RMVar_hsa_circ_62319,RMVar_hsa_circ_353766,RMVar_hsa_circ_201097,RMVar_hsa_circ_279267,RMVar_hsa_circ_201102 103542 RMVar_ID_103542 Human_SNP_ID_77304302 m1A Human chr2 - 72132223 72132223 72132223 CGGAGGCCATGCTGAGCGCCACAGTCTAACCCAAGACCCACCCGCCTCAGCCCAGCCCAGGCAGC CGGAGGCCATGCTGAGCGCCACAGTCTAACCCGAGACCCACCCGCCTCAGCCCAGCCCAGGCAGC T C CYP26B1 Ensembl:ENSG00000003137 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:72132174..72132282 26863196 MeRIP-seq:(Medium) rs1212576157 Functional Loss SNV dbSNP153 33..33 33 - - - 103543 RMVar_ID_103543 Human_SNP_ID_77307911 m1A Human chr2 - 72144119 72144112 72144119 GGGGCGGCCGCTGATACGCGTGACCGGCGCGGAGAACGTGCGCAAGATCCTCATGGGCGAGCACC GGGGCGGCCGCTGATACGCGTGACCGGCGCGG_______GCGCAAGATCCTCATGGGCGAGCACC CACGTTCT C CYP26B1 Ensembl:ENSG00000003137 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:72144071..72144277 26863196 MeRIP-seq:(Medium) rs757748581 Functional Loss DEL dbSNP153 33..39 33 - - - Human_Splice_Rec_261526 RMVar_hsa_circ_201119,RMVar_hsa_circ_280625 103544 RMVar_ID_103544 Human_SNP_ID_77307915 m1A Human chr2 - 72144119 72144119 72144119 GGGGCGGCCGCTGATACGCGTGACCGGCGCGGAGAACGTGCGCAAGATCCTCATGGGCGAGCACC GGGGCGGCCGCTGATACGCGTGACCGGCGCGGGGAACGTGCGCAAGATCCTCATGGGCGAGCACC T C CYP26B1 Ensembl:ENSG00000003137 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:72144071..72144277 26863196 MeRIP-seq:(Medium) rs1282504686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_261526 RMVar_hsa_circ_201119,RMVar_hsa_circ_280625 103545 RMVar_ID_103545 Human_SNP_ID_77309452 m1A Human chr2 + 72148676 72148667 72148676 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGCGGGAGGGGTGAGGCGGGGTGGGGTTG GCGGCGGCGGCGGCGGCGGCGGCG_________GCGGGCGGGAGGGGTGAGGCGGGGTGGGGTTG GGCGGCGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr2:72148541..72148879;chr2:72148568..72148754 26863196 MeRIP-seq:(Medium) rs1345520720 Functional Loss DEL dbSNP153 25..33 33 - - - 103546 RMVar_ID_103546 Human_SNP_ID_77309460 m1A Human chr2 + 72148676 72148676 72148676 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGCGGGAGGGGTGAGGCGGGGTGGGGTTG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGCGGGAGGGGTGAGGCGGGGTGGGGTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr2:72148541..72148879;chr2:72148568..72148754 26863196 MeRIP-seq:(Medium) rs1239017490 Functional Loss SNV dbSNP153 33..33 33 - - - 103547 RMVar_ID_103547 Human_SNP_ID_77475709 m1A Human chr2 - 72887467 72887467 72887467 GCGTCCGGCCGAAGCCGCGGGAGGCCCCGGTCAGCAAGCACACAGCACGCCCCAGCCCGCCCTCC GCGTCCGGCCGAAGCCGCGGGAGGCCCCGGTCGGCAAGCACACAGCACGCCCCAGCCCGCCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:72887401..72887625 26863196 MeRIP-seq:(Medium) rs1486552702 Functional Loss SNV dbSNP153 33..33 33 - - - 103548 RMVar_ID_103548 Human_SNP_ID_77493318 m1A Human chr2 - 72959180 72959180 72959180 GGAGGTGTCTGCATTGAGCTCACAAGAAGGCGAGGGCTGTGGCCAGAAAGCGGCGCTTCTGAATC GGAGGTGTCTGCATTGAGCTCACAAGAAGGCGGGGGCTGTGGCCAGAAAGCGGCGCTTCTGAATC T C SFXN5 Ensembl:ENSG00000144040 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:72959178..72959355 26863196 MeRIP-seq:(Medium) rs987067384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69157,RMVar_hsa_circ_354881,RMVar_hsa_circ_64253 103549 RMVar_ID_103549 Human_SNP_ID_77493359 m1A Human chr2 + 72959390 72959390 72959390 AAGGATCTGTGGCCCTCCCTGTACTGGCCCATAGCACCTCCTGGTGAACAGGCCCGGCTGCACTC AAGGATCTGTGGCCCTCCCTGTACTGGCCCATGGCACCTCCTGGTGAACAGGCCCGGCTGCACTC A G lnc-EMX1-1,lnc-EMX1-1:2 RNACentral:URS00009C4E09,RNACentral:URS00009C28B0 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:72959388..72959471 26863196 MeRIP-seq:(Medium) rs1289076591 Functional Loss SNV dbSNP153 33..33 33 - - - 103550 RMVar_ID_103550 Human_SNP_ID_77493366 m1A Human chr2 - 72959416 72959416 72959416 AGGAGGCTGAGCAGCACGTGGTCTGGGAGTGCAGCCGGGCCTGTTCACCAGGAGGTGCTATGGGC AGGAGGCTGAGCAGCACGTGGTCTGGGAGTGCGGCCGGGCCTGTTCACCAGGAGGTGCTATGGGC T C SFXN5 Ensembl:ENSG00000144040 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:72959413..72959485 26863196 MeRIP-seq:(Medium) rs1471444486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3639862,Human_RBP_ID_8202168 RMVar_hsa_circ_69157,RMVar_hsa_circ_354881,RMVar_hsa_circ_64253 103551 RMVar_ID_103551 Human_SNP_ID_77516319 m1A Human chr2 - 73053389 73053389 73053389 AAAAAAACAGCGGGAAGGAGAGCATGATACTGAGATGAGCTGAAAGACCAATAAAGAAATGCCAC AAAAAAACAGCGGGAAGGAGAGCATGATACTGTGATGAGCTGAAAGACCAATAAAGAAATGCCAC T A SFXN5 Ensembl:ENSG00000144040 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73053378..73053463 26863196 MeRIP-seq:(Medium) rs1203873617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13959193,Human_RBP_ID_23884361 RMVar_hsa_circ_69157,RMVar_hsa_circ_296581,RMVar_hsa_circ_201182,RMVar_hsa_circ_336695,RMVar_hsa_circ_201186,RMVar_hsa_circ_302236,RMVar_hsa_circ_115265,RMVar_hsa_circ_201189,RMVar_hsa_circ_201190,RMVar_hsa_circ_57708,RMVar_hsa_circ_280041,RMVar_hsa_circ_201191,RMVar_hsa_circ_303794,RMVar_hsa_circ_201194,RMVar_hsa_circ_300341,RMVar_hsa_circ_376887,RMVar_hsa_circ_201195 103552 RMVar_ID_103552 Human_SNP_ID_77520461 m1A Human chr2 + 73070441 73070436 73070441 TCCCCTTCCACCACAACAACAAAAAAAGAAAAAAAAAGCCACCGCACCGACCTTAGCACAATTTC TCCCCTTCCACCACAACAACAAAAAAAG_____AAAAGCCACCGCACCGACCTTAGCACAATTTC GAAAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73070434..73070653 26863196 MeRIP-seq:(Medium) rs1161712706 Functional Loss DEL dbSNP153 29..33 33 - - - 103553 RMVar_ID_103553 Human_SNP_ID_77520462 m1A Human chr2 + 73070441 73070436 73070441 TCCCCTTCCACCACAACAACAAAAAAAGAAAAAAAAAGCCACCGCACCGACCTTAGCACAATTTC TCCCCTTCCACCACAACAACAAAAAAAGAAAA_AAAAGCCACCGCACCGACCTTAGCACAATTTC GAAAAA GAAAA - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73070434..73070653 26863196 MeRIP-seq:(Medium) rs1161712706 Functional Loss DEL dbSNP153 33..33 33 - - - 103554 RMVar_ID_103554 Human_SNP_ID_77520466 m1A Human chr2 + 73070441 73070441 73070441 TCCCCTTCCACCACAACAACAAAAAAAGAAAAAAAAAGCCACCGCACCGACCTTAGCACAATTTC TCCCCTTCCACCACAACAACAAAAAAAGAAAATAAAAGCCACCGCACCGACCTTAGCACAATTTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73070434..73070653 26863196 MeRIP-seq:(Medium) rs1193113353 Functional Loss SNV dbSNP153 33..33 33 - - - 103555 RMVar_ID_103555 Human_SNP_ID_77520989 m1A Human chr2 - 73071687 73071687 73071687 GGGCGTCAGTGGCCATGGCGGATACAGCGACTACAGCATCGGCGGCGGCGGCTAGTGCCGCTAGC GGGCGTCAGTGGCCATGGCGGATACAGCGACTGCAGCATCGGCGGCGGCGGCTAGTGCCGCTAGC T C SFXN5 Ensembl:ENSG00000144040 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73071624..73071716 26863196 MeRIP-seq:(Medium) rs533416003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_261791,Human_Splice_Rec_261841,Human_Splice_Rec_261863,Human_Splice_Rec_261909,Human_Splice_Rec_261945,Human_Splice_Rec_261961,Human_Splice_Rec_262031 RMVar_hsa_circ_115265,RMVar_hsa_circ_201190 103556 RMVar_ID_103556 Human_SNP_ID_77521611 m1A Human chr2 - 73073830 73073830 73073830 TCTGCTGCCAGGATGGAGCAGAGGAGCGCCACACATGGAGGAAAGCCCCTGTAACGTTACCTACC TCTGCTGCCAGGATGGAGCAGAGGAGCGCCACGCATGGAGGAAAGCCCCTGTAACGTTACCTACC T C SFXN5,RAB11FIP5 Ensembl:ENSG00000144040,Ensembl:ENSG00000135631 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:73073779..73073929 32194978 MeRIP-seq:(Medium) rs1022378841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128032,RMVar_hsa_circ_201196,RMVar_hsa_circ_102179,RMVar_hsa_circ_118891,RMVar_hsa_circ_201197,RMVar_hsa_circ_201198 103557 RMVar_ID_103557 Human_SNP_ID_77521756 m1A Human chr2 - 73074463 73074463 73074463 ACAGCACTGCTGTGGGCTGTTCCCCTCCCCTAAAGTTAATCTCTTGGTCTGGCCAAGTTGCTGCT ACAGCACTGCTGTGGGCTGTTCCCCTCCCCTATAGTTAATCTCTTGGTCTGGCCAAGTTGCTGCT T A SFXN5,RAB11FIP5 Ensembl:ENSG00000144040,Ensembl:ENSG00000135631 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:73074276..73074674 32194978 MeRIP-seq:(Medium) rs1291235401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128032,RMVar_hsa_circ_201196,RMVar_hsa_circ_102179,RMVar_hsa_circ_118891,RMVar_hsa_circ_201197,RMVar_hsa_circ_201198 103558 RMVar_ID_103558 Human_SNP_ID_77521762 m1A Human chr2 - 73074490 73074490 73074490 CTCTCAGGGCCCTGGGAATGGGAATGGACAGCACTGCTGTGGGCTGTTCCCCTCCCCTAAAGTTA CTCTCAGGGCCCTGGGAATGGGAATGGACAGCGCTGCTGTGGGCTGTTCCCCTCCCCTAAAGTTA T C SFXN5,RAB11FIP5 Ensembl:ENSG00000144040,Ensembl:ENSG00000135631 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1992133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23884391 Human_miRNA_ID_327995,Human_miRNA_ID_332016,Human_miRNA_ID_349096,Human_miRNA_ID_1512119,Human_miRNA_ID_1642301,Human_miRNA_ID_2773355 GWAS_ID_13439,GWAS_ID_13440,GWAS_ID_13441 RMVar_hsa_circ_128032,RMVar_hsa_circ_201196,RMVar_hsa_circ_102179,RMVar_hsa_circ_118891,RMVar_hsa_circ_201197,RMVar_hsa_circ_201198 103559 RMVar_ID_103559 Human_SNP_ID_77521811 m1A Human chr2 - 73074689 73074689 73074689 GCTTATGATTTGGGGATCAAGCCTCCATGTCTATTCTTGTTGCCTGTCCAGATGCCAAAACTCTG GCTTATGATTTGGGGATCAAGCCTCCATGTCTGTTCTTGTTGCCTGTCCAGATGCCAAAACTCTG T C SFXN5,RAB11FIP5 Ensembl:ENSG00000144040,Ensembl:ENSG00000135631 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1046183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13959232 GWAS_ID_13442,GWAS_ID_13443,GWAS_ID_13444 RMVar_hsa_circ_128032,RMVar_hsa_circ_201196,RMVar_hsa_circ_102179,RMVar_hsa_circ_118891,RMVar_hsa_circ_201197,RMVar_hsa_circ_201198 103560 RMVar_ID_103560 Human_SNP_ID_77523630 m1A Human chr2 + 73081516 73081516 73081516 GCGGTGGTGGCGGCAGCGGCAGCAGTGGCAGCAGCGGGGGAGGCGGCTGCAAAAAGGTTAGTGCT GCGGTGGTGGCGGCAGCGGCAGCAGTGGCAGCCGCGGGGGAGGCGGCTGCAAAAAGGTTAGTGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73081514..73081588 26863196 MeRIP-seq:(Medium) rs1434877562 Functional Loss SNV dbSNP153 33..33 33 - - - 103561 RMVar_ID_103561 Human_SNP_ID_77525182 m1A Human chr2 - 73088350 73088350 73088350 CCTGGCCCCTGGGGCCAGCCACCCTGGAGAGGAGGAGGGGGCCCGGCTACCAGAGGGCAAGCCAG CCTGGCCCCTGGGGCCAGCCACCCTGGAGAGGCGGAGGGGGCCCGGCTACCAGAGGGCAAGCCAG T G RAB11FIP5 Ensembl:ENSG00000135631 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73088300..73088420 26863196 MeRIP-seq:(Medium) rs369090487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5147466 Human_miRNA_ID_730457,Human_miRNA_ID_2294880 RMVar_hsa_circ_128032,RMVar_hsa_circ_201198,RMVar_hsa_circ_270194,RMVar_hsa_circ_343149,RMVar_hsa_circ_201199 103562 RMVar_ID_103562 Human_SNP_ID_77525204 m1A Human chr2 - 73088407 73088407 73088407 CAACAGCAGCTCAGAGGCAGTGCTTGGACAGGAGGAGCTGAGTGCTCAGGCTAAAGTCCTGGCCC CAACAGCAGCTCAGAGGCAGTGCTTGGACAGGGGGAGCTGAGTGCTCAGGCTAAAGTCCTGGCCC T C RAB11FIP5 Ensembl:ENSG00000135631 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73088357..73088477 26863196 MeRIP-seq:(Medium) rs138135562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128032,RMVar_hsa_circ_201198,RMVar_hsa_circ_270194,RMVar_hsa_circ_343149,RMVar_hsa_circ_201199 103563 RMVar_ID_103563 Human_SNP_ID_77556157 m1A Human chr2 - 73214294 73214292 73214295 CCGCGCGCGGCCCGCCACGCCCACGCAGAAGGAGAACACGTCGCACATGGAGGCCGCCATCTTGG CCGCGCGCGGCCCGCCACGCCCACGCAGAAG___AACACGTCGCACATGGAGGCCGCCATCTTGG TCTC T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:73214263..73214353 26863410 MeRIP-seq:(Medium) rs759226759 Functional Loss DEL dbSNP153 32..34 33 - - - 103564 RMVar_ID_103564 Human_SNP_ID_77556160 m1A Human chr2 - 73214298 73214295 73214298 AGACCCGCGCGCGGCCCGCCACGCCCACGCAGAAGGAGAACACGTCGCACATGGAGGCCGCCATC AGACCCGCGCGCGGCCCGCCACGCCCACGCAG___GAGAACACGTCGCACATGGAGGCCGCCATC CCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73214251..73214802 26863196 MeRIP-seq:(Medium) rs766987772 Functional Loss DEL dbSNP153 33..35 33 - - - 103565 RMVar_ID_103565 Human_SNP_ID_77556164 m1A Human chr2 - 73214298 73214298 73214298 AGACCCGCGCGCGGCCCGCCACGCCCACGCAGAAGGAGAACACGTCGCACATGGAGGCCGCCATC AGACCCGCGCGCGGCCCGCCACGCCCACGCAGGAGGAGAACACGTCGCACATGGAGGCCGCCATC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73214251..73214802 26863196 MeRIP-seq:(Medium) rs1558549998 Functional Loss SNV dbSNP153 33..33 33 - - - 103566 RMVar_ID_103566 Human_SNP_ID_77556198 m1A Human chr2 + 73214361 73214361 73214361 CTCCGTGGAAGTCCGTTTCGTGAGCAGCGCCAAGGTGAGGTCGGGGCGGGTCCTGCCGGGAGCCT CTCCGTGGAAGTCCGTTTCGTGAGCAGCGCCAGGGTGAGGTCGGGGCGGGTCCTGCCGGGAGCCT A G SMYD5 Ensembl:ENSG00000135632 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:73214261..73214400 26863196 MeRIP-seq:(Medium) rs1359498610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622457,Human_RBP_ID_5381124,Human_RBP_ID_19097625,Human_RBP_ID_26787013 Human_Splice_Rec_262075,Human_Splice_Rec_262083,Human_Splice_Rec_262097,Human_Splice_Rec_262121 103567 RMVar_ID_103567 Human_SNP_ID_77556248 m1A Human chr2 - 73214471 73214471 73214471 AGCCCCCGGGCCGCGAGCAGGGGCAGGGCCGTAGCGTCCGAGCGGCACAGAAGCCTCTGGGCTCC AGCCCCCGGGCCGCGAGCAGGGGCAGGGCCGTGGCGTCCGAGCGGCACAGAAGCCTCTGGGCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73214463..73214657 26863196 MeRIP-seq:(Medium) rs1558550137 Functional Loss SNV dbSNP153 33..33 33 - - - 103568 RMVar_ID_103568 Human_SNP_ID_77557282 m1A Human chr2 - 73218812 73218811 73218813 ATAGGATGGCCATAAAAAGGAACAGAAGACATAGCTCCGAGAGCTTCCAGGAGGCTGTCCAGCCT ATAGGATGGCCATAAAAAGGAACAGAAGACA__GCTCCGAGAGCTTCCAGGAGGCTGTCCAGCCT CTA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73218809..73218889 26863196 MeRIP-seq:(Medium) rs764510692 Functional Loss DEL dbSNP153 32..33 33 - - - 103569 RMVar_ID_103569 Human_SNP_ID_77559199 m1A Human chr2 + 73225897 73225895 73225898 AGAAGAGGAAGAGGAAGAGGAGGAGGAGGAGGAAGGAGAGCCAGAAGATGCAGAGCTGGGGGATG AGAAGAGGAAGAGGAAGAGGAGGAGGAGGAG___GGAGAGCCAGAAGATGCAGAGCTGGGGGATG GGAA G SMYD5 Ensembl:ENSG00000135632 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73225847..73225941 26863196 MeRIP-seq:(Medium) rs757115976 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5527735,Human_RBP_ID_19001832,Human_RBP_ID_22451365,Human_RBP_ID_27481622 Human_miRNA_ID_336858,Human_miRNA_ID_2082356 RMVar_hsa_circ_113656,RMVar_hsa_circ_91711,RMVar_hsa_circ_201202,RMVar_hsa_circ_119720,RMVar_hsa_circ_201203,RMVar_hsa_circ_201205 103570 RMVar_ID_103570 Human_SNP_ID_77559896 m1A Human chr2 + 73228573 73228573 73228573 CCCATGCTGTTCCAGAGAGCGGCGGATCATGTAGCTGGGAGGGCATGAAGAGAGGTGGTGACGGT CCCATGCTGTTCCAGAGAGCGGCGGATCATGTCGCTGGGAGGGCATGAAGAGAGGTGGTGACGGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:73228538..73228953 32194978 MeRIP-seq:(Medium) rs1272162480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555229,Human_RBP_ID_13959455 103571 RMVar_ID_103571 Human_SNP_ID_77561152 m1A Human chr2 + 73233105 73233105 73233105 GTCCCACCCGTTGCCGCTCACCGTGGGCCGCGACGCACGCGGGGAGCCAGAGCACGAGACAACAC GTCCCACCCGTTGCCGCTCACCGTGGGCCGCGGCGCACGCGGGGAGCCAGAGCACGAGACAACAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73230163..73233231 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 103572 RMVar_ID_103572 Human_SNP_ID_77561153 m1A Human chr2 + 73233105 73233105 73233105 GTCCCACCCGTTGCCGCTCACCGTGGGCCGCGACGCACGCGGGGAGCCAGAGCACGAGACAACAC GTCCCACCCGTTGCCGCTCACCGTGGGCCGCGTCGCACGCGGGGAGCCAGAGCACGAGACAACAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73230163..73233231 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 103573 RMVar_ID_103573 Human_SNP_ID_77561573 m1A Human chr2 - 73234352 73234352 73234352 CATCATTTTGGAAGCTTATTCAGCGGCCCGCCACTCTCCCCTCTTCTCCGAGACCGGGCCGCCCA CATCATTTTGGAAGCTTATTCAGCGGCCCGCCGCTCTCCCCTCTTCTCCGAGACCGGGCCGCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73234301..73234439 26863196 MeRIP-seq:(Medium) rs750318883 Functional Loss SNV dbSNP153 33..33 33 - - - 103574 RMVar_ID_103574 Human_SNP_ID_77561574 m1A Human chr2 - 73234352 73234352 73234352 CATCATTTTGGAAGCTTATTCAGCGGCCCGCCACTCTCCCCTCTTCTCCGAGACCGGGCCGCCCA CATCATTTTGGAAGCTTATTCAGCGGCCCGCCCCTCTCCCCTCTTCTCCGAGACCGGGCCGCCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73234301..73234439 26863196 MeRIP-seq:(Medium) rs750318883 Functional Loss SNV dbSNP153 33..33 33 - - - 103575 RMVar_ID_103575 Human_SNP_ID_77561593 m1A Human chr2 + 73234365 73234365 73234365 CTCGGAGAAGAGGGGAGAGTGGCGGGCCGCTGAATAAGCTTCCAAAATGATGGTGAGTGGCGTCT CTCGGAGAAGAGGGGAGAGTGGCGGGCCGCTGCATAAGCTTCCAAAATGATGGTGAGTGGCGTCT A C CCT7 Ensembl:ENSG00000135624 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73234301..73234453 26863196 MeRIP-seq:(Medium) rs550584392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143428,Human_RBP_ID_555235,Human_RBP_ID_1302272,Human_RBP_ID_4615952,Human_RBP_ID_5322100,Human_RBP_ID_8851935,Human_RBP_ID_9296603,Human_RBP_ID_9330513,Human_RBP_ID_18421825 Human_Splice_Rec_262201,Human_Splice_Rec_262219,Human_Splice_Rec_262243,Human_Splice_Rec_262251,Human_Splice_Rec_262253,Human_Splice_Rec_262263,Human_Splice_Rec_262275,Human_Splice_Rec_262297,Human_Splice_Rec_262303,Human_Splice_Rec_262313 Human_miRNA_ID_2204833,Human_miRNA_ID_2928565 RMVar_hsa_circ_109279,RMVar_hsa_circ_201210 103576 RMVar_ID_103576 Human_SNP_ID_77561594 m1A Human chr2 + 73234365 73234365 73234365 CTCGGAGAAGAGGGGAGAGTGGCGGGCCGCTGAATAAGCTTCCAAAATGATGGTGAGTGGCGTCT CTCGGAGAAGAGGGGAGAGTGGCGGGCCGCTGGATAAGCTTCCAAAATGATGGTGAGTGGCGTCT A G CCT7 Ensembl:ENSG00000135624 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73234301..73234453 26863196 MeRIP-seq:(Medium) rs550584392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143428,Human_RBP_ID_555235,Human_RBP_ID_1302272,Human_RBP_ID_4615952,Human_RBP_ID_5322100,Human_RBP_ID_8851935,Human_RBP_ID_9296603,Human_RBP_ID_9330513,Human_RBP_ID_18421825 Human_Splice_Rec_262201,Human_Splice_Rec_262219,Human_Splice_Rec_262243,Human_Splice_Rec_262251,Human_Splice_Rec_262253,Human_Splice_Rec_262263,Human_Splice_Rec_262275,Human_Splice_Rec_262297,Human_Splice_Rec_262303,Human_Splice_Rec_262313 Human_miRNA_ID_2204833,Human_miRNA_ID_2928565 RMVar_hsa_circ_109279,RMVar_hsa_circ_201210 103577 RMVar_ID_103577 Human_SNP_ID_77561604 m1A Human chr2 - 73234386 73234386 73234386 GCTGATGGCGACGGATGCGCGAGACGCCACTCACCATCATTTTGGAAGCTTATTCAGCGGCCCGC GCTGATGGCGACGGATGCGCGAGACGCCACTCGCCATCATTTTGGAAGCTTATTCAGCGGCCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr2:73234301..73234446;chr2:73234326..73234449 26863410 MeRIP-seq:(Medium) rs1273145904 Functional Loss SNV dbSNP153 33..33 33 - - - 103578 RMVar_ID_103578 Human_SNP_ID_77562925 m1A Human chr2 + 73239606 73239606 73239606 TCCCCTTTCCCCTGCCAGTCTCATTATAATAGATGATTATTAAAAGCAGTTAATTTCTTTCTTTT TCCCCTTTCCCCTGCCAGTCTCATTATAATAGGTGATTATTAAAAGCAGTTAATTTCTTTCTTTT A G CCT7 Ensembl:ENSG00000135624 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:73239602..73239775 26863410 MeRIP-seq:(Medium) rs377610448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109279,RMVar_hsa_circ_34057,RMVar_hsa_circ_201210 103579 RMVar_ID_103579 Human_SNP_ID_77562930 m1A Human chr2 - 73239629 73239626 73239630 ATAGGATAACTGGTGTGGGCTAGAAAAGAAAGAAATTAACTGCTTTTAATAATCATCTATTATAA ATAGGATAACTGGTGTGGGCTAGAAAAGAAA____TTAACTGCTTTTAATAATCATCTATTATAA ATTTC A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr2:73239626..73239675;chr2:73239626..73239700 26863196,32194978 MeRIP-seq:(Medium) rs758414021 Functional Loss DEL dbSNP153 32..35 33 - - - 103580 RMVar_ID_103580 Human_SNP_ID_77563136 m1A Human chr2 + 73240445 73240445 73240445 AGATTTTTGTTTGTTTCTTTTAAGGCAAAGCAACAATTTCTAATGATGGGGCCACAATTCTGAAA AGATTTTTGTTTGTTTCTTTTAAGGCAAAGCACCAATTTCTAATGATGGGGCCACAATTCTGAAA A C CCT7 Ensembl:ENSG00000135624 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:73240426..73240475;chr2:73240426..73240500 26863196 MeRIP-seq:(Medium) rs748537266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1196898,Human_RBP_ID_1923152,Human_RBP_ID_3633952,Human_RBP_ID_6948253,Human_RBP_ID_8109211,Human_RBP_ID_8524955,Human_RBP_ID_17276780,Human_RBP_ID_17391904,Human_RBP_ID_17960999,Human_RBP_ID_18765412,Human_RBP_ID_27481644 Human_Splice_Rec_262174,Human_Splice_Rec_262175,Human_Splice_Rec_262180,Human_Splice_Rec_262181,Human_Splice_Rec_262192,Human_Splice_Rec_262198,Human_Splice_Rec_262199,Human_Splice_Rec_262224,Human_Splice_Rec_262225,Human_Splice_Rec_262246,Human_Splice_Rec_262247,Human_Splice_Rec_262258,Human_Splice_Rec_262259,Human_Splice_Rec_262278,Human_Splice_Rec_262279,Human_Splice_Rec_262300,Human_Splice_Rec_262301,Human_Splice_Rec_262328,Human_Splice_Rec_262329 RMVar_hsa_circ_109279,RMVar_hsa_circ_201211,RMVar_hsa_circ_316496,RMVar_hsa_circ_34057,RMVar_hsa_circ_201210,RMVar_hsa_circ_353834,RMVar_hsa_circ_375353,RMVar_hsa_circ_13309,RMVar_hsa_circ_314531,RMVar_hsa_circ_201212,RMVar_hsa_circ_201213,RMVar_hsa_circ_67625 103581 RMVar_ID_103581 Human_SNP_ID_77564022 m1A Human chr2 + 73243980 73243980 73243980 GCAGTTTGTCTTTAGCATGAGAGACTCATTCAACTTCTGTTCTTGGCAGGCAGTTAACAAGATCA GCAGTTTGTCTTTAGCATGAGAGACTCATTCAGCTTCTGTTCTTGGCAGGCAGTTAACAAGATCA A G CCT7 Ensembl:ENSG00000135624 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:73243976..73244050 32194978 MeRIP-seq:(Medium) rs764877727 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_13959697 Human_Splice_Rec_262185,Human_Splice_Rec_262205,Human_Splice_Rec_262229,Human_Splice_Rec_262283,Human_Splice_Rec_262309,Human_Splice_Rec_262317,Human_Splice_Rec_262333 RMVar_hsa_circ_316496,RMVar_hsa_circ_353834,RMVar_hsa_circ_375353,RMVar_hsa_circ_201212,RMVar_hsa_circ_201213,RMVar_hsa_circ_323078,RMVar_hsa_circ_67625,RMVar_hsa_circ_358003,RMVar_hsa_circ_201214 103582 RMVar_ID_103582 Human_SNP_ID_77564958 m1A Human chr2 - 73247723 73247723 73247723 TAAAAAAACAAACACTTTAATGGTTTGGTACTAACATGAAATAAAATCAAGCTAGTTGTTTGCTG TAAAAAAACAAACACTTTAATGGTTTGGTACTCACATGAAATAAAATCAAGCTAGTTGTTTGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73247721..73247856 26863196 MeRIP-seq:(Medium) rs758434119 Functional Loss SNV dbSNP153 33..33 33 - - - 103583 RMVar_ID_103583 Human_SNP_ID_77565313 m1A Human chr2 - 73249175 73249175 73249175 GAGAAGCAGCCTGTGAAAATCTGGTTACCATCATTGTCCTCTTCAGATCCTCCTCAGGTACTCGG GAGAAGCAGCCTGTGAAAATCTGGTTACCATCGTTGTCCTCTTCAGATCCTCCTCAGGTACTCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73249039..73249228 26863196 MeRIP-seq:(Medium) rs768639367 Functional Loss SNV dbSNP153 33..33 33 - - - 103584 RMVar_ID_103584 Human_SNP_ID_77565696 m1A Human chr2 - 73250380 73250380 73250380 TGGCATCATGCAGGGACCGCTCTGTCTCCTCCATAAACTGCTCGGCGCCGCCACGGAGAATGAAG TGGCATCATGCAGGGACCGCTCTGTCTCCTCCGTAAACTGCTCGGCGCCGCCACGGAGAATGAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73250272..73250482 26863196 MeRIP-seq:(Medium) rs1387147324 Functional Loss SNV dbSNP153 33..33 33 - - - 103585 RMVar_ID_103585 Human_SNP_ID_77565931 m1A Human chr2 - 73251302 73251302 73251302 ATGCCCCAATCAACAGCTGCTGTTTTCCTGGAATAGTCCTTGAGTAATCCCGCAGGTACTTGGAG ATGCCCCAATCAACAGCTGCTGTTTTCCTGGAGTAGTCCTTGAGTAATCCCGCAGGTACTTGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:73251251..73251450 32194978 MeRIP-seq:(Medium) rs375292953 Functional Loss SNV dbSNP153 33..33 33 - - - 103586 RMVar_ID_103586 Human_SNP_ID_77570629 m1A Human chr2 - 73268819 73268819 73268819 CGAGAAGGAGGAGCTGGAGGAGCGCGCGTCTGAGCTCTCCCGCCAGGTGGACGTGAGCGTAGAGC CGAGAAGGAGGAGCTGGAGGAGCGCGCGTCTGTGCTCTCCCGCCAGGTGGACGTGAGCGTAGAGC T A FBXO41 Ensembl:ENSG00000163013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73268769..73269113 26863196 MeRIP-seq:(Medium) rs1444956105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918184,Human_RBP_ID_19001854,Human_RBP_ID_22997367,Human_RBP_ID_27481673 Human_Splice_Rec_262339,Human_Splice_Rec_262361,Human_Splice_Rec_262385 103587 RMVar_ID_103587 Human_SNP_ID_77571823 m1A Human chr2 - 73273048 73273048 73273048 CCCTCCTAGTTGAAGAGGGGGGTGAGGAAAAAAACCTGGACCGTGGTCCACATGCTTGACTGAAT CCCTCCTAGTTGAAGAGGGGGGTGAGGAAAAACACCTGGACCGTGGTCCACATGCTTGACTGAAT T G FBXO41 Ensembl:ENSG00000163013 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73273016..73273147 26863196 MeRIP-seq:(Medium) rs905039007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555299,Human_RBP_ID_19001860 Human_Splice_Rec_262412,Human_Splice_Rec_262413 103588 RMVar_ID_103588 Human_SNP_ID_77574274 m1A Human chr2 - 73284315 73284315 73284315 TGGGAGGTTCGGCCGCCCCCGCCCCGAGAGGGAGGCGGGGGCGCTAGCCGCGGCGGCCACCCAAG TGGGAGGTTCGGCCGCCCCCGCCCCGAGAGGGGGGCGGGGGCGCTAGCCGCGGCGGCCACCCAAG T C FBXO41 Ensembl:ENSG00000163013 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73284264..73284435 26863196 MeRIP-seq:(Medium) rs889433681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622460,Human_RBP_ID_18422250 103589 RMVar_ID_103589 Human_SNP_ID_77574342 m1A Human chr2 + 73284448 73284448 73284448 GGGGAGGAGGGGGCGCGCGGGCCGAGGAAAGCAAGGGAAGGGGGAGGGAGGCAGCACCGAGGTGG GGGGAGGAGGGGGCGCGCGGGCCGAGGAAAGCTAGGGAAGGGGGAGGGAGGCAGCACCGAGGTGG A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:73284397..73284532 26863410 MeRIP-seq:(Medium) rs1385263950 Functional Loss SNV dbSNP153 33..33 33 - - - 103590 RMVar_ID_103590 Human_SNP_ID_77597768 m1A Human chr2 + 73385981 73385981 73385981 GGAGGCTGCAGCGGCGGCGGCGGCGAACGTGGACGACGTAGTGGTCGTGGAGGAGGTGGAGGAAG GGAGGCTGCAGCGGCGGCGGCGGCGAACGTGGGCGACGTAGTGGTCGTGGAGGAGGTGGAGGAAG A G ALMS1 Ensembl:ENSG00000116127 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73385874..73386144 26863196 MeRIP-seq:(Medium) rs1462829116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527746,Human_RBP_ID_19001861 103591 RMVar_ID_103591 Human_SNP_ID_77597778 m1A Human chr2 - 73385993 73385993 73385993 CCCGCCCCGCCTCTTCCTCCACCTCCTCCACGACCACTACGTCGTCCACGTTCGCCGCCGCCGCC CCCGCCCCGCCTCTTCCTCCACCTCCTCCACGTCCACTACGTCGTCCACGTTCGCCGCCGCCGCC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:73385942..73386071 26863196 MeRIP-seq:(Medium) rs1337322908 Functional Loss SNV dbSNP153 33..33 33 - - - 103592 RMVar_ID_103592 Human_SNP_ID_77598357 m1A Human chr2 - 73387703 73387703 73387703 TATACACCTGACCTTTCTGAAACACCTAACTTATCATACATCCCCTCGTTTCAAATATTTTCTTC TATACACCTGACCTTTCTGAAACACCTAACTTGTCATACATCCCCTCGTTTCAAATATTTTCTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73387691..73388045 26863196 MeRIP-seq:(Medium) rs1214767056 Functional Loss SNV dbSNP153 33..33 33 - - - 103593 RMVar_ID_103593 Human_SNP_ID_77617547 m1A Human chr2 - 73458764 73458764 73458764 TTCCACAATCTAGTCTTCTCCCTTTCACTCTCACTCTCCAAACACACTGGCCTCCTCCCTTTCCT TTCCACAATCTAGTCTTCTCCCTTTCACTCTCTCTCTCCAAACACACTGGCCTCCTCCCTTTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73458643..73458841 26863196 MeRIP-seq:(Medium) rs891096622 Functional Loss SNV dbSNP153 33..33 33 - - - 103594 RMVar_ID_103594 Human_SNP_ID_77696069 m1A Human chr2 - 73736864 73736864 73736864 GAGCTTAGAGAAGGCCATTGCGGCGGTAGCAGAAGAGGAGAGGCAGGGACCAGATCGTAGAGTGT GAGCTTAGAGAAGGCCATTGCGGCGGTAGCAGGAGAGGAGAGGCAGGGACCAGATCGTAGAGTGT T C TPRKB Ensembl:ENSG00000144034 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:73736850..73737046 26863196 MeRIP-seq:(Medium) rs1052736630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555375 103595 RMVar_ID_103595 Human_SNP_ID_77707236 m1A Human chr2 + 73780047 73780047 73780047 AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGATAAGACCCTAAACAGGAAAAGACTCGGCAGCC AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGCTAAGACCCTAAACAGGAAAAGACTCGGCAGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73779936..73780065 26863196 MeRIP-seq:(Medium) rs562414734 Functional Loss SNV dbSNP153 33..33 33 - - - 103596 RMVar_ID_103596 Human_SNP_ID_77707237 m1A Human chr2 + 73780047 73780047 73780047 AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGATAAGACCCTAAACAGGAAAAGACTCGGCAGCC AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGGTAAGACCCTAAACAGGAAAAGACTCGGCAGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73779936..73780065 26863196 MeRIP-seq:(Medium) rs562414734 Functional Loss SNV dbSNP153 33..33 33 - - - 103597 RMVar_ID_103597 Human_SNP_ID_77707238 m1A Human chr2 + 73780047 73780047 73780047 AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGATAAGACCCTAAACAGGAAAAGACTCGGCAGCC AAAAGCGCCAGTCCGGCGCCCTCAATGCCAGGTTAAGACCCTAAACAGGAAAAGACTCGGCAGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73779936..73780065 26863196 MeRIP-seq:(Medium) rs562414734 Functional Loss SNV dbSNP153 33..33 33 - - - 103598 RMVar_ID_103598 Human_SNP_ID_77707246 m1A Human chr2 + 73780052 73780052 73780052 CGCCAGTCCGGCGCCCTCAATGCCAGGATAAGACCCTAAACAGGAAAAGACTCGGCAGCCACCTA CGCCAGTCCGGCGCCCTCAATGCCAGGATAAGGCCCTAAACAGGAAAAGACTCGGCAGCCACCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73779940..73780065 26863196 MeRIP-seq:(Medium) rs770537593 Functional Loss SNV dbSNP153 33..33 33 - - - 103599 RMVar_ID_103599 Human_SNP_ID_77715882 m1A Human chr2 + 73829270 73829270 73829270 TGGGGTTGGCAAGTTCGTCTTGAGTGCCTTCAAGAAGGGTTCCTCAAGCAGTTGTCGATAGAGCC TGGGGTTGGCAAGTTCGTCTTGAGTGCCTTCAGGAAGGGTTCCTCAAGCAGTTGTCGATAGAGCC A G STAMBP Ensembl:ENSG00000124356 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:73829266..73829357 26863196 MeRIP-seq:(Medium) rs573027904 Functional Loss SNV dbSNP153 33..33 33 - - - 103600 RMVar_ID_103600 Human_SNP_ID_77732519 m1A Human chr2 - 73895053 73895053 73895053 CCTGGTGCCGCCCTCTTCCCTCCCAACCTATCACCAGCCCTTCTTACTTCTACCTGCACGGCACC CCTGGTGCCGCCCTCTTCCCTCCCAACCTATCGCCAGCCCTTCTTACTTCTACCTGCACGGCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73895051..73895321 26863196 MeRIP-seq:(Medium) rs60188129 Functional Loss SNV dbSNP153 33..33 33 - - - 103601 RMVar_ID_103601 Human_SNP_ID_77732520 m1A Human chr2 - 73895053 73895053 73895053 CCTGGTGCCGCCCTCTTCCCTCCCAACCTATCACCAGCCCTTCTTACTTCTACCTGCACGGCACC CCTGGTGCCGCCCTCTTCCCTCCCAACCTATCCCCAGCCCTTCTTACTTCTACCTGCACGGCACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73895051..73895321 26863196 MeRIP-seq:(Medium) rs60188129 Functional Loss SNV dbSNP153 33..33 33 - - - 103602 RMVar_ID_103602 Human_SNP_ID_77734766 m1A Human chr2 + 73902451 73902451 73902451 GCGAGGGATCCTAACTCTCAAATACCCCATTGAACACGGCATCATCACCAACTGGGATGACATGG GCGAGGGATCCTAACTCTCAAATACCCCATTGTACACGGCATCATCACCAACTGGGATGACATGG A T ACTG2 Ensembl:ENSG00000163017 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73902401..73902535 26863196 MeRIP-seq:(Medium) rs1290993369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_263018,Human_Splice_Rec_263019,Human_Splice_Rec_263034,Human_Splice_Rec_263060,Human_Splice_Rec_263061,Human_Splice_Rec_263066,Human_Splice_Rec_263067,Human_Splice_Rec_263074,Human_Splice_Rec_263075,Human_Splice_Rec_263092,Human_Splice_Rec_263093 RMVar_hsa_circ_38868,RMVar_hsa_circ_91543,RMVar_hsa_circ_101791,RMVar_hsa_circ_94495,RMVar_hsa_circ_76232,RMVar_hsa_circ_201262,RMVar_hsa_circ_201263,RMVar_hsa_circ_201261,RMVar_hsa_circ_112119,RMVar_hsa_circ_201264,RMVar_hsa_circ_106131,RMVar_hsa_circ_116425,RMVar_hsa_circ_201265,RMVar_hsa_circ_201266,RMVar_hsa_circ_201267 103603 RMVar_ID_103603 Human_SNP_ID_77741565 m1A Human chr2 - 73926927 73926927 73926927 AACTGAAGGGTGCTCGAAGCCGACTTAGAAAGAGGCGGCCCGCGGCCATCCCACCCACGATTCAC AACTGAAGGGTGCTCGAAGCCGACTTAGAAAGTGGCGGCCCGCGGCCATCCCACCCACGATTCAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73926876..73927075 26863196 MeRIP-seq:(Medium) rs372855715 Functional Loss SNV dbSNP153 33..33 33 - - - 103604 RMVar_ID_103604 Human_SNP_ID_77741573 m1A Human chr2 - 73926937 73926937 73926937 TTGGCCATGGAACTGAAGGGTGCTCGAAGCCGACTTAGAAAGAGGCGGCCCGCGGCCATCCCACC TTGGCCATGGAACTGAAGGGTGCTCGAAGCCGTCTTAGAAAGAGGCGGCCCGCGGCCATCCCACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73926886..73926992 26863196 MeRIP-seq:(Medium) rs768840084 Functional Loss SNV dbSNP153 33..33 33 - - - 103605 RMVar_ID_103605 Human_SNP_ID_77741579 m1A Human chr2 + 73926946 73926946 73926946 GCCGCGGGCCGCCTCTTTCTAAGTCGGCTTCGAGCACCCTTCAGTTCCATGGCCAAGAGCCCACT GCCGCGGGCCGCCTCTTTCTAAGTCGGCTTCGCGCACCCTTCAGTTCCATGGCCAAGAGCCCACT A C DGUOK Ensembl:ENSG00000114956 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:73926901..73927063 26863196 MeRIP-seq:(Medium) rs1442447487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555452,Human_RBP_ID_1590250,Human_RBP_ID_4623405,Human_RBP_ID_9330518,Human_RBP_ID_13963223,Human_RBP_ID_18765645,Human_RBP_ID_22452304,Human_RBP_ID_23211613 103606 RMVar_ID_103606 Human_SNP_ID_77741605 m1A Human chr2 - 73926995 73926995 73926995 TCGGGGCCCGCGCCCCGCGTGCAGGCCTCTGGAGGAGGAAACGCCCTCGAGTGGGCTCTTGGCCA TCGGGGCCCGCGCCCCGCGTGCAGGCCTCTGGGGGAGGAAACGCCCTCGAGTGGGCTCTTGGCCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:73926901..73927050 26863196 MeRIP-seq:(Medium) rs1204952716 Functional Loss SNV dbSNP153 33..33 33 - - - 103607 RMVar_ID_103607 Human_SNP_ID_77741630 m1A Human chr2 - 73927038 73927038 73927038 CCGCTTTCCGGCCCTTACCAATGTTGCCTTCGATGGAGAGCCTTCGGGGCCCGCGCCCCGCGTGC CCGCTTTCCGGCCCTTACCAATGTTGCCTTCGGTGGAGAGCCTTCGGGGCCCGCGCCCCGCGTGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:73926919..73927075 26863196 MeRIP-seq:(Medium) rs1558637583 Functional Loss SNV dbSNP153 33..33 33 - - - 103608 RMVar_ID_103608 Human_SNP_ID_77746397 m1A Human chr2 - 73946738 73946738 73946738 GCTCCCGGTACATCATATCCAGCAAGTTTCCAAGACTTTGGGCAGTGCAGGCCTAGAGGGAGATG GCTCCCGGTACATCATATCCAGCAAGTTTCCACGACTTTGGGCAGTGCAGGCCTAGAGGGAGATG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:73946728..73946923 32194978 MeRIP-seq:(Medium) rs982717858 Functional Loss SNV dbSNP153 33..33 33 - - - 103609 RMVar_ID_103609 Human_SNP_ID_77747677 m1A Human chr2 + 73952430 73952430 73952430 CTCAAAGAGGACAGTTTGAAGTGTCAAAGTGTAGGGTTCAAGTTGGGAGAGAAGTCCTGAGCCCC CTCAAAGAGGACAGTTTGAAGTGTCAAAGTGTGGGGTTCAAGTTGGGAGAGAAGTCCTGAGCCCC A G DGUOK Ensembl:ENSG00000114956 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73952428..73952615 26863196 MeRIP-seq:(Medium) rs1476454149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71332,RMVar_hsa_circ_332373,RMVar_hsa_circ_117246,RMVar_hsa_circ_278264,RMVar_hsa_circ_201275,RMVar_hsa_circ_201276,RMVar_hsa_circ_357914 103610 RMVar_ID_103610 Human_SNP_ID_77749457 m1A Human chr2 + 73958810 73958810 73958810 TTTCTGAAGCTAGAAAAATGTTGTGTCTCCCAACCACCTTTCCATCCCCAGCCCCTCTCATCCCT TTTCTGAAGCTAGAAAAATGTTGTGTCTCCCAGCCACCTTTCCATCCCCAGCCCCTCTCATCCCT A G DGUOK Ensembl:ENSG00000114956 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73958763..73958862 26863196 MeRIP-seq:(Medium) rs768586756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555479,Human_RBP_ID_1099038,Human_RBP_ID_1241393,Human_RBP_ID_1590265,Human_RBP_ID_8948962,Human_RBP_ID_17276835,Human_RBP_ID_17658490,Human_RBP_ID_17961264,Human_RBP_ID_18765665,Human_RBP_ID_18947973,Human_RBP_ID_23211614,Human_RBP_ID_23282334 Human_miRNA_ID_2683103 RMVar_hsa_circ_201277,RMVar_hsa_circ_117246,RMVar_hsa_circ_201275,RMVar_hsa_circ_201276 103611 RMVar_ID_103611 Human_SNP_ID_77754583 m1A Human chr2 - 73978953 73978953 73978953 AGAGAGGTATCAAGAAAGATTTACGAAGTCAAACCCACAGGACGAGGGCATAGGAAGGGAGGTTT AGAGAGGTATCAAGAAAGATTTACGAAGTCAAGCCCACAGGACGAGGGCATAGGAAGGGAGGTTT T C DGUOK-AS1 Ensembl:ENSG00000237883 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:73978916..73979021 26863196 MeRIP-seq:(Medium) rs1280228431 Functional Loss SNV dbSNP153 33..33 33 - - - 103612 RMVar_ID_103612 Human_SNP_ID_77756110 m1A Human chr2 - 73985020 73985020 73985020 CGCCTCCCGGAGCGCCCGGCCCGACCGAGCTCAGCGCGCGGAGCCCCCCGCCCGGGCCGAGGAGG CGCCTCCCGGAGCGCCCGGCCCGACCGAGCTCGGCGCGCGGAGCCCCCCGCCCGGGCCGAGGAGG T C DGUOK-AS1,DGUOK-AS1:2,DGUOK-AS1:3,DGUOK-AS1:4,DGUOK-AS1:5 RNACentral:URS0000D5B9EA,RNACentral:URS0000D5D333,RNACentral:URS0000D5BBEC,RNACentral:URS00008B4ACD,RNACentral:URS0000D5D0D4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr2:73984917..73985122;chr2:73984982..73985114 26863196 MeRIP-seq:(Medium) rs34604399 Functional Loss SNV dbSNP153 33..33 33 - - - 103613 RMVar_ID_103613 Human_SNP_ID_77756161 m1A Human chr2 - 73985120 73985120 73985120 CGCCGCCTCCGGGGCGGAGCGCACAAAGGGGCAAAGTTTCCCGGCCCGCGCCGCCGCCGCCACCA CGCCGCCTCCGGGGCGGAGCGCACAAAGGGGCGAAGTTTCCCGGCCCGCGCCGCCGCCGCCACCA T C DGUOK-AS1,DGUOK-AS1:2,DGUOK-AS1:3,DGUOK-AS1:4,DGUOK-AS1:5 RNACentral:URS0000D5B9EA,RNACentral:URS0000D5D333,RNACentral:URS0000D5BBEC,RNACentral:URS00008B4ACD,RNACentral:URS0000D5D0D4 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73984843..73985174 26863196 MeRIP-seq:(Medium) rs1279680592 Functional Loss SNV dbSNP153 33..33 33 - - - 103614 RMVar_ID_103614 Human_SNP_ID_77756207 m1A Human chr2 + 73985245 73985222 73985245 GCGGGGGGCCCGGCCCGGGGGAGGGGGAGGGGACGGCCCGGATCCGGCGGGGGGCCGCTCCTCCG GCGGGGGGCC_______________________CGGCCCGGATCCGGCGGGGGGCCGCTCCTCCG CCGGCCCGGGGGAGGGGGAGGGGA C AC073046.1 Ensembl:ENSG00000235499 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:73985178..73985283 26863410 MeRIP-seq:(Medium) rs1044859893 Functional Loss DEL dbSNP153 11..33 33 - - - Human_RBP_ID_8200581,Human_RBP_ID_18422254,Human_RBP_ID_26787018 103615 RMVar_ID_103615 Human_SNP_ID_77760105 m1A Human chr2 - 73999943 73999941 73999944 TCGGCTACACCAGAGAAGTAGCCCAGAGGAGGAGCCCATAGTCCCCCAGGCAGTCCATCTGCTCC TCGGCTACACCAGAGAAGTAGCCCAGAGGAG___CCCATAGTCCCCCAGGCAGTCCATCTGCTCC GCTC G DGUOK-AS1 RNACentral:URS00008B4ACD lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73999936..74000105 26863196 MeRIP-seq:(Medium) rs370189460 Functional Loss DEL dbSNP153 32..34 33 - - - 103616 RMVar_ID_103616 Human_SNP_ID_77761189 m1A Human chr2 - 74003713 74003713 74003713 GACGCCCGCCGGATTCCCAGTCATGATGTTGCATCAGCCCCCACCCTACCCAAAATATCCTCACC GACGCCCGCCGGATTCCCAGTCATGATGTTGCGTCAGCCCCCACCCTACCCAAAATATCCTCACC T C DGUOK-AS1 RNACentral:URS00008B4ACD lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74003691..74003975 26863196 MeRIP-seq:(Medium) rs1431838701 Functional Loss SNV dbSNP153 33..33 33 - - - 103617 RMVar_ID_103617 Human_SNP_ID_77761199 m1A Human chr2 - 74003744 74003744 74003744 CCTAGACACCAAGTCACACAGAGTAACAGCAGACGCCCGCCGGATTCCCAGTCATGATGTTGCAT CCTAGACACCAAGTCACACAGAGTAACAGCAGTCGCCCGCCGGATTCCCAGTCATGATGTTGCAT T A DGUOK-AS1 RNACentral:URS00008B4ACD lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74003711..74003824 26863196 MeRIP-seq:(Medium) rs922569523 Functional Loss SNV dbSNP153 33..33 33 - - - 103618 RMVar_ID_103618 Human_SNP_ID_77768558 m1A Human chr2 - 74032323 74032323 74032323 GGGCATTCTCACAACTCCTCCCACCCAACAGCACAGATCTACTCCTCATCACCCACACCTCCTAC GGGCATTCTCACAACTCCTCCCACCCAACAGCGCAGATCTACTCCTCATCACCCACACCTCCTAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74032321..74032430 26863196 MeRIP-seq:(Medium) rs1343562170 Functional Loss SNV dbSNP153 33..33 33 - - - 103619 RMVar_ID_103619 Human_SNP_ID_77770709 m1A Human chr2 + 74040112 74040112 74040112 CACGTATTAAGCACTCGATGCATATGAATGGCATTCTTAAACTGAAGATTGAAGCCAGGGTGGAC CACGTATTAAGCACTCGATGCATATGAATGGCGTTCTTAAACTGAAGATTGAAGCCAGGGTGGAC A G TET3 Ensembl:ENSG00000187605 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74040108..74040284 26863196 MeRIP-seq:(Medium) rs1022513229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315910 103620 RMVar_ID_103620 Human_SNP_ID_77785064 m1A Human chr2 - 74094266 74094266 74094266 CCTGCACACACGCTGGTCCCTCTGCCTGGAGCACTCTACCCCCAGATAGTGGCTCTCTCACTCTC CCTGCACACACGCTGGTCCCTCTGCCTGGAGCCCTCTACCCCCAGATAGTGGCTCTCTCACTCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74094237..74094765 26863196 MeRIP-seq:(Medium) rs1224064461 Functional Loss SNV dbSNP153 33..33 33 - - - 103621 RMVar_ID_103621 Human_SNP_ID_77787421 m1A Human chr2 + 74101599 74101599 74101599 TGGGGCTCTGAAGTCAGAGGAGAAGCTGTGGGACCCCTTCAGCCTGGAGGAGGGGCCGGCTGAGG TGGGGCTCTGAAGTCAGAGGAGAAGCTGTGGGCCCCCTTCAGCCTGGAGGAGGGGCCGGCTGAGG A C TET3 Ensembl:ENSG00000187605 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74101552..74101651 26863196 MeRIP-seq:(Medium) rs774476922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527823,Human_RBP_ID_6949670,Human_RBP_ID_27481784 RMVar_hsa_circ_89843,RMVar_hsa_circ_113503,RMVar_hsa_circ_201281,RMVar_hsa_circ_201282,RMVar_hsa_circ_201283,RMVar_hsa_circ_121894 103622 RMVar_ID_103622 Human_SNP_ID_77787422 m1A Human chr2 + 74101599 74101599 74101599 TGGGGCTCTGAAGTCAGAGGAGAAGCTGTGGGACCCCTTCAGCCTGGAGGAGGGGCCGGCTGAGG TGGGGCTCTGAAGTCAGAGGAGAAGCTGTGGGTCCCCTTCAGCCTGGAGGAGGGGCCGGCTGAGG A T TET3 Ensembl:ENSG00000187605 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74101552..74101651 26863196 MeRIP-seq:(Medium) rs774476922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527823,Human_RBP_ID_6949670,Human_RBP_ID_27481784 RMVar_hsa_circ_89843,RMVar_hsa_circ_113503,RMVar_hsa_circ_201281,RMVar_hsa_circ_201282,RMVar_hsa_circ_201283,RMVar_hsa_circ_121894 103623 RMVar_ID_103623 Human_SNP_ID_77787433 m1A Human chr2 + 74101629 74101629 74101629 GGACCCCTTCAGCCTGGAGGAGGGGCCGGCTGAGGAGCCCCCCAGCAAGGGAGCGGTGAAGGAGG GGACCCCTTCAGCCTGGAGGAGGGGCCGGCTGGGGAGCCCCCCAGCAAGGGAGCGGTGAAGGAGG A G TET3 Ensembl:ENSG00000187605 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74101580..74101786 26863196 MeRIP-seq:(Medium) rs753647592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5527823 RMVar_hsa_circ_89843,RMVar_hsa_circ_113503,RMVar_hsa_circ_201281,RMVar_hsa_circ_201282,RMVar_hsa_circ_201283,RMVar_hsa_circ_121894 103624 RMVar_ID_103624 Human_SNP_ID_77787441 m1A Human chr2 + 74101648 74101648 74101648 GAGGGGCCGGCTGAGGAGCCCCCCAGCAAGGGAGCGGTGAAGGAGGAGAAGGGCGGTGGTGGTGC GAGGGGCCGGCTGAGGAGCCCCCCAGCAAGGGCGCGGTGAAGGAGGAGAAGGGCGGTGGTGGTGC A C TET3 Ensembl:ENSG00000187605 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74101601..74101746 26863196 MeRIP-seq:(Medium) rs1428781868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89843,RMVar_hsa_circ_113503,RMVar_hsa_circ_201281,RMVar_hsa_circ_201282,RMVar_hsa_circ_201283,RMVar_hsa_circ_121894 103625 RMVar_ID_103625 Human_SNP_ID_77787564 m1A Human chr2 + 74101965 74101965 74101965 GCTGGCGGAGAGGGCACGGGCACGGCAGGAGGAGGCTGCCCGGCTGGGCCTGGGCCAGCAGGAGG GCTGGCGGAGAGGGCACGGGCACGGCAGGAGGCGGCTGCCCGGCTGGGCCTGGGCCAGCAGGAGG A C TET3 Ensembl:ENSG00000187605 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74101915..74102063 26863196 MeRIP-seq:(Medium) rs565203881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242139,Human_RBP_ID_5527826 RMVar_hsa_circ_89843,RMVar_hsa_circ_113503,RMVar_hsa_circ_201281,RMVar_hsa_circ_201282,RMVar_hsa_circ_201283,RMVar_hsa_circ_121894 103626 RMVar_ID_103626 Human_SNP_ID_77792703 m1A Human chr2 + 74120623 74120623 74120623 TGAGGAGCCCAAGGAGCGGGGCGGCGGCCACTAGGAGCTCAGGAGGCAAGGGCGTGGCCGAGTGG TGAGGAGCCCAAGGAGCGGGGCGGCGGCCACTCGGAGCTCAGGAGGCAAGGGCGTGGCCGAGTGG A C lnc-TET3-3 RNACentral:URS00008B4F74 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74120574..74120688 26863196 MeRIP-seq:(Medium) rs1228953397 Functional Loss SNV dbSNP153 33..33 33 - - - 103627 RMVar_ID_103627 Human_SNP_ID_77800112 m1A Human chr2 + 74147776 74147776 74147776 CCCGACAGCCGCCGGCCCCGCGGTCCCTCCGCAGCTCCCGTCCCGGGGAGAGCAGCCCCGACCCT CCCGACAGCCGCCGGCCCCGCGGTCCCTCCGCGGCTCCCGTCCCGGGGAGAGCAGCCCCGACCCT A G BOLA3-AS1,BOLA3-AS1:2 RNACentral:URS00008B46A3,RNACentral:URS00009B972E lincRNA,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:74147773..74147950 26863410 MeRIP-seq:(Medium) rs1336494751 Functional Loss SNV dbSNP153 33..33 33 - - - 103628 RMVar_ID_103628 Human_SNP_ID_77800163 m1A Human chr2 + 74147869 74147869 74147869 AGGAGAGGCGCTGCCGCGGCCGGGCTCCATGCAGCCATGCCCGGCCGACGTGACCCGCCGCCCGA AGGAGAGGCGCTGCCGCGGCCGGGCTCCATGCGGCCATGCCCGGCCGACGTGACCCGCCGCCCGA A G BOLA3-AS1,BOLA3-AS1:2 RNACentral:URS00008B46A3,RNACentral:URS00009B972E lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:74147777..74147925;chr2:74147697..74147934;chr2:74147742..74147925;chr2:74147762..74147925 26863196 MeRIP-seq:(Medium) rs768012977 Functional Loss SNV dbSNP153 33..33 33 - - - 103629 RMVar_ID_103629 Human_SNP_ID_77808194 m1A Human chr2 + 74178727 74178727 74178727 GCGAGGGGCCCCTGGCCCCCGCCTGGATCAGGATTCGGAGCTGGCTAGAGGGAGCGGACCGTCCT GCGAGGGGCCCCTGGCCCCCGCCTGGATCAGGGTTCGGAGCTGGCTAGAGGGAGCGGACCGTCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74178676..74178800 32194978 MeRIP-seq:(Medium) rs563556740 Functional Loss SNV dbSNP153 33..33 33 - - - 103630 RMVar_ID_103630 Human_SNP_ID_77808230 m1A Human chr2 - 74178835 74178835 74178835 CGAGGTGGGGTAGGCGGGCAAGGCGGGCGCCGAGGTTTGCAAAGGCTCGCAGCGGCCAGAAACCC CGAGGTGGGGTAGGCGGGCAAGGCGGGCGCCGGGGTTTGCAAAGGCTCGCAGCGGCCAGAAACCC T C MOB1A Ensembl:ENSG00000114978 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74178729..74178875 26863196 MeRIP-seq:(Medium) rs966268448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828636,Human_RBP_ID_4616644,Human_RBP_ID_18421827,Human_RBP_ID_22449863 RMVar_hsa_circ_110470,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_201295 103631 RMVar_ID_103631 Human_SNP_ID_77813572 m1A Human chr2 + 74198651 74198651 74198651 CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGACTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGCCTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG A C MTHFD2 Ensembl:ENSG00000065911 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74198601..74198700 26863196 MeRIP-seq:(Medium) rs780949855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555681,Human_RBP_ID_774551,Human_RBP_ID_1024185,Human_RBP_ID_1590349,Human_RBP_ID_4616648,Human_RBP_ID_5275734,Human_RBP_ID_5423276,Human_RBP_ID_5445121,Human_RBP_ID_5502587,Human_RBP_ID_6950144,Human_RBP_ID_8109289,Human_RBP_ID_8525412,Human_RBP_ID_8849923,Human_RBP_ID_9330524,Human_RBP_ID_13965287,Human_RBP_ID_17392714,Human_RBP_ID_18765751,Human_RBP_ID_23885497,Human_RBP_ID_26818613,Human_RBP_ID_27698494 Human_Splice_Rec_263297,Human_Splice_Rec_263305,Human_Splice_Rec_263317,Human_Splice_Rec_263325,Human_Splice_Rec_263335,Human_Splice_Rec_263349,Human_Splice_Rec_263359 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296 103632 RMVar_ID_103632 Human_SNP_ID_77813573 m1A Human chr2 + 74198651 74198651 74198651 CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGACTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGGCTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG A G MTHFD2 Ensembl:ENSG00000065911 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74198601..74198700 26863196 MeRIP-seq:(Medium) rs780949855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555681,Human_RBP_ID_774551,Human_RBP_ID_1024185,Human_RBP_ID_1590349,Human_RBP_ID_4616648,Human_RBP_ID_5275734,Human_RBP_ID_5423276,Human_RBP_ID_5445121,Human_RBP_ID_5502587,Human_RBP_ID_6950144,Human_RBP_ID_8109289,Human_RBP_ID_8525412,Human_RBP_ID_8849923,Human_RBP_ID_9330524,Human_RBP_ID_13965287,Human_RBP_ID_17392714,Human_RBP_ID_18765751,Human_RBP_ID_23885497,Human_RBP_ID_26818613,Human_RBP_ID_27698494 Human_Splice_Rec_263297,Human_Splice_Rec_263305,Human_Splice_Rec_263317,Human_Splice_Rec_263325,Human_Splice_Rec_263335,Human_Splice_Rec_263349,Human_Splice_Rec_263359 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296 103633 RMVar_ID_103633 Human_SNP_ID_77813615 m1A Human chr2 + 74198697 74198697 74198697 TGCTTTGGCTGCCCGGCTGCTGCAGCCCGCGCACAGCTGCTCCCTTCGCCTTCGCCCTTTCCACC TGCTTTGGCTGCCCGGCTGCTGCAGCCCGCGCCCAGCTGCTCCCTTCGCCTTCGCCCTTTCCACC A C MTHFD2 Ensembl:ENSG00000065911 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:74198601..74198750 26863410 MeRIP-seq:(Medium) rs1473434678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555681,Human_RBP_ID_774552,Human_RBP_ID_827233,Human_RBP_ID_1590353,Human_RBP_ID_4616649,Human_RBP_ID_6950146,Human_RBP_ID_8525414,Human_RBP_ID_8849924,Human_RBP_ID_9330524,Human_RBP_ID_17276890,Human_RBP_ID_17392715,Human_RBP_ID_18765753,Human_RBP_ID_22076407,Human_RBP_ID_22816218,Human_RBP_ID_26818614,Human_RBP_ID_27014856 Human_Splice_Rec_263297,Human_Splice_Rec_263305,Human_Splice_Rec_263317,Human_Splice_Rec_263325,Human_Splice_Rec_263335,Human_Splice_Rec_263349,Human_Splice_Rec_263359 Human_miRNA_ID_2249883 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296 103634 RMVar_ID_103634 Human_SNP_ID_77816635 m1A Human chr2 + 74210024 74210024 74210024 GTTGGAATGCCCATTGCAATGTTACTGCACACAGATGGGGCGCATGAACGTCCCGGAGGTAAGGA GTTGGAATGCCCATTGCAATGTTACTGCACACGGATGGGGCGCATGAACGTCCCGGAGGTAAGGA A G MTHFD2 Ensembl:ENSG00000065911 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74207819..74211227 32194978 MeRIP-seq:(Medium) rs775072112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242197,Human_RBP_ID_827236,Human_RBP_ID_1590397,Human_RBP_ID_5117960,Human_RBP_ID_17277800,Human_RBP_ID_17392720,Human_RBP_ID_19097664,Human_RBP_ID_22669128,Human_RBP_ID_23885525,Human_RBP_ID_26819887 Human_Splice_Rec_263310,Human_Splice_Rec_263311,Human_Splice_Rec_263328,Human_Splice_Rec_263329,Human_Splice_Rec_263342,Human_Splice_Rec_263343,Human_Splice_Rec_263354,Human_Splice_Rec_263355,Human_Splice_Rec_263366 RMVar_hsa_circ_39818,RMVar_hsa_circ_84324,RMVar_hsa_circ_201296,RMVar_hsa_circ_99083,RMVar_hsa_circ_323806,RMVar_hsa_circ_24330,RMVar_hsa_circ_349359,RMVar_hsa_circ_124533,RMVar_hsa_circ_201298,RMVar_hsa_circ_201299,RMVar_hsa_circ_201300 103635 RMVar_ID_103635 Human_SNP_ID_77817963 m1A Human chr2 + 74214466 74214428 74214467 ATCATGCAGGGTCCTGTGATCTAGCCAGGAGCAGCCATTAACCTAGTGATTAATATGGGAGACAT __________________________________CCATTAACCTAGTGATTAATATGGGAGACAT TCCAGTATCATGCAGGGTCCTGTGATCTAGCCAGGAGCAG T MTHFD2 Ensembl:ENSG00000065911 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74214416..74214487 26863196 MeRIP-seq:(Medium) rs1411984096 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_555761,Human_RBP_ID_774564,Human_RBP_ID_1024214,Human_RBP_ID_1590431,Human_RBP_ID_1923500,Human_RBP_ID_3634487,Human_RBP_ID_6950384,Human_RBP_ID_8525456,Human_RBP_ID_9110806,Human_RBP_ID_13965914,Human_RBP_ID_17276909,Human_RBP_ID_17392024,Human_RBP_ID_17508749,Human_RBP_ID_17961493,Human_RBP_ID_22505919,Human_RBP_ID_23211617,Human_RBP_ID_23885550,Human_RBP_ID_26818630,Human_RBP_ID_27698525 Human_miRNA_ID_258219,Human_miRNA_ID_262014 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296,RMVar_hsa_circ_99083,RMVar_hsa_circ_124533,RMVar_hsa_circ_201299,RMVar_hsa_circ_126876,RMVar_hsa_circ_115920,RMVar_hsa_circ_201300,RMVar_hsa_circ_201301,RMVar_hsa_circ_90581,RMVar_hsa_circ_201303,RMVar_hsa_circ_201304 103636 RMVar_ID_103636 Human_SNP_ID_77817975 m1A Human chr2 + 74214466 74214466 74214466 ATCATGCAGGGTCCTGTGATCTAGCCAGGAGCAGCCATTAACCTAGTGATTAATATGGGAGACAT ATCATGCAGGGTCCTGTGATCTAGCCAGGAGCGGCCATTAACCTAGTGATTAATATGGGAGACAT A G MTHFD2 Ensembl:ENSG00000065911 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74214416..74214487 26863196 MeRIP-seq:(Medium) rs1228546953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555761,Human_RBP_ID_774564,Human_RBP_ID_1024214,Human_RBP_ID_1590431,Human_RBP_ID_1923500,Human_RBP_ID_3634487,Human_RBP_ID_6950384,Human_RBP_ID_8525456,Human_RBP_ID_9110806,Human_RBP_ID_13965914,Human_RBP_ID_17276909,Human_RBP_ID_17392024,Human_RBP_ID_17508749,Human_RBP_ID_17961493,Human_RBP_ID_22505919,Human_RBP_ID_23211617,Human_RBP_ID_23885550,Human_RBP_ID_26818630,Human_RBP_ID_27698525 Human_miRNA_ID_258219,Human_miRNA_ID_262014 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296,RMVar_hsa_circ_99083,RMVar_hsa_circ_124533,RMVar_hsa_circ_201299,RMVar_hsa_circ_126876,RMVar_hsa_circ_115920,RMVar_hsa_circ_201300,RMVar_hsa_circ_201301,RMVar_hsa_circ_90581,RMVar_hsa_circ_201303,RMVar_hsa_circ_201304 103637 RMVar_ID_103637 Human_SNP_ID_77854393 m1A Human chr2 - 74362113 74362110 74362113 CTAGGATGAGGTCCTCAAGGAGACAGTATCTCAGCGCCCTGGAGCCACAGTACCCACTGACTTTG CTAGGATGAGGTCCTCAAGGAGACAGTATCTC___GCCCTGGAGCCACAGTACCCACTGACTTTG CGCT C AC006030.1,DCTN1 Ensembl:ENSG00000264324,Ensembl:ENSG00000204843 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74362062..74362173 26863196 MeRIP-seq:(Medium) rs1364182022 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_829554,Human_RBP_ID_922289,Human_RBP_ID_9386843,Human_RBP_ID_18999672,Human_RBP_ID_22451390,Human_RBP_ID_22595696 Human_Splice_Rec_263372,Human_Splice_Rec_263373,Human_Splice_Rec_263962,Human_Splice_Rec_263963,Human_Splice_Rec_264022,Human_Splice_Rec_264023,Human_Splice_Rec_264082,Human_Splice_Rec_264083,Human_Splice_Rec_264090,Human_Splice_Rec_264091,Human_Splice_Rec_264144,Human_Splice_Rec_264145,Human_Splice_Rec_264196,Human_Splice_Rec_264197,Human_Splice_Rec_264246,Human_Splice_Rec_264247,Human_Splice_Rec_264300,Human_Splice_Rec_264301,Human_Splice_Rec_264360,Human_Splice_Rec_264361,Human_Splice_Rec_264398,Human_Splice_Rec_264399,Human_Splice_Rec_264452,Human_Splice_Rec_264453,Human_Splice_Rec_264456 RMVar_hsa_circ_95900,RMVar_hsa_circ_201310,RMVar_hsa_circ_105012,RMVar_hsa_circ_97781,RMVar_hsa_circ_127386,RMVar_hsa_circ_93991,RMVar_hsa_circ_201315,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_201318,RMVar_hsa_circ_201322,RMVar_hsa_circ_90269,RMVar_hsa_circ_92205,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_201319,RMVar_hsa_circ_201316,RMVar_hsa_circ_201317 103638 RMVar_ID_103638 Human_SNP_ID_77854710 m1A Human chr2 - 74362961 74362961 74362961 GTATGTACCTGCCAACCCCCAAGATGAATAAAACTGCCCCCTCCACTTGGCCCAGGGATTTAGCC GTATGTACCTGCCAACCCCCAAGATGAATAAAGCTGCCCCCTCCACTTGGCCCAGGGATTTAGCC T C AC006030.1,DCTN1 Ensembl:ENSG00000264324,Ensembl:ENSG00000204843 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74362953..74363155 26863196 MeRIP-seq:(Medium) rs766499131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19097667 RMVar_hsa_circ_95900,RMVar_hsa_circ_201310,RMVar_hsa_circ_105012,RMVar_hsa_circ_127386,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_44977,RMVar_hsa_circ_201318,RMVar_hsa_circ_201322,RMVar_hsa_circ_90269,RMVar_hsa_circ_92205,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_201319,RMVar_hsa_circ_201317,RMVar_hsa_circ_111003,RMVar_hsa_circ_201324 103639 RMVar_ID_103639 Human_SNP_ID_77855811 m1A Human chr2 - 74366272 74366272 74366272 GAACAAGCTGGCCACAGCCATGCAGGAGGGGGAGTATGATGCAGAGCGGCCCCCCAGCAAGGTAG GAACAAGCTGGCCACAGCCATGCAGGAGGGGGCGTATGATGCAGAGCGGCCCCCCAGCAAGGTAG T G DCTN1 Ensembl:ENSG00000204843 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74366258..74366409 32194978 MeRIP-seq:(Medium) rs1368703951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555872,Human_RBP_ID_915565,Human_RBP_ID_8851334,Human_RBP_ID_9297298,Human_RBP_ID_26339451 Human_Splice_Rec_263947,Human_Splice_Rec_264007,Human_Splice_Rec_264069,Human_Splice_Rec_264131,Human_Splice_Rec_264181,Human_Splice_Rec_264233,Human_Splice_Rec_264287,Human_Splice_Rec_264347,Human_Splice_Rec_264387,Human_Splice_Rec_264439,Human_Splice_Rec_264469 Human_miRNA_ID_1358672,Human_miRNA_ID_2093906,Human_miRNA_ID_2093907,Human_miRNA_ID_2394379,Human_miRNA_ID_2394380,Human_miRNA_ID_2717970,Human_miRNA_ID_2717971 RMVar_hsa_circ_95900,RMVar_hsa_circ_127386,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_201318,RMVar_hsa_circ_201322,RMVar_hsa_circ_92205,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_201319,RMVar_hsa_circ_111003,RMVar_hsa_circ_111366,RMVar_hsa_circ_126896,RMVar_hsa_circ_115995,RMVar_hsa_circ_201324,RMVar_hsa_circ_201325,RMVar_hsa_circ_201327,RMVar_hsa_circ_91946,RMVar_hsa_circ_201326,RMVar_hsa_circ_201328 103640 RMVar_ID_103640 Human_SNP_ID_77856018 m1A Human chr2 - 74366836 74366836 74366836 TCCGCCAGTTCTGCAAGAAGATCCGAAGGCGAATGCCAGGGACAGATGCTCCTGGGATCCCAGCT TCCGCCAGTTCTGCAAGAAGATCCGAAGGCGAGTGCCAGGGACAGATGCTCCTGGGATCCCAGCT T C DCTN1 Ensembl:ENSG00000204843 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74366757..74368195 32194978 MeRIP-seq:(Medium) rs755946834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8851337,Human_RBP_ID_9110838,Human_RBP_ID_9297301,Human_RBP_ID_18470800,Human_RBP_ID_19001878,Human_RBP_ID_22816236,Human_RBP_ID_26339452,Human_RBP_ID_27014900 Human_Splice_Rec_263942,Human_Splice_Rec_263943,Human_Splice_Rec_264002,Human_Splice_Rec_264003,Human_Splice_Rec_264064,Human_Splice_Rec_264065,Human_Splice_Rec_264128,Human_Splice_Rec_264129,Human_Splice_Rec_264176,Human_Splice_Rec_264177,Human_Splice_Rec_264228,Human_Splice_Rec_264229,Human_Splice_Rec_264282,Human_Splice_Rec_264283,Human_Splice_Rec_264342,Human_Splice_Rec_264343,Human_Splice_Rec_264384,Human_Splice_Rec_264434,Human_Splice_Rec_264435,Human_Splice_Rec_264466,Human_Splice_Rec_264467 RMVar_hsa_circ_95900,RMVar_hsa_circ_127386,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_201318,RMVar_hsa_circ_201322,RMVar_hsa_circ_92205,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_201319,RMVar_hsa_circ_111003,RMVar_hsa_circ_81991,RMVar_hsa_circ_111366,RMVar_hsa_circ_126896,RMVar_hsa_circ_115995,RMVar_hsa_circ_201324,RMVar_hsa_circ_201325,RMVar_hsa_circ_201327,RMVar_hsa_circ_91946,RMVar_hsa_circ_201326,RMVar_hsa_circ_201328,RMVar_hsa_circ_201330 103641 RMVar_ID_103641 Human_SNP_ID_77856918 m1A Human chr2 + 74369447 74369447 74369447 TCCAGCTGCTCCCGCAGCTCCAGTTCTGTCTCACGTGCATTCTCCTGCAGCTCATCGTTCATCTC TCCAGCTGCTCCCGCAGCTCCAGTTCTGTCTCCCGTGCATTCTCCTGCAGCTCATCGTTCATCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74369311..74369534 26863196 MeRIP-seq:(Medium) rs138045336 Functional Loss SNV dbSNP153 33..33 33 - - - 103642 RMVar_ID_103642 Human_SNP_ID_77857107 m1A Human chr2 + 74369996 74369996 74369996 CCAAGTCTCCCACAGTCTCCCTCAACTCGCGCACTTTCTCTTCCAGATTCAGGTTCCGATCTGTC CCAAGTCTCCCACAGTCTCCCTCAACTCGCGCCCTTTCTCTTCCAGATTCAGGTTCCGATCTGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74369301..74370350 26863196 MeRIP-seq:(Medium) rs1446602495 Functional Loss SNV dbSNP153 33..33 33 - - - 103643 RMVar_ID_103643 Human_SNP_ID_77857185 m1A Human chr2 - 74370235 74370235 74370235 GGAAGTTGTGAGGCAACAGCGGGAGCGTCTGCAGGAGGAGCTAAGCCAGGCAGAGAGCACCATTG GGAAGTTGTGAGGCAACAGCGGGAGCGTCTGCGGGAGGAGCTAAGCCAGGCAGAGAGCACCATTG T C DCTN1 Ensembl:ENSG00000204843 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74370152..74370302 26863196 MeRIP-seq:(Medium) rs745458066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60594,Human_RBP_ID_243271,Human_RBP_ID_922312,Human_RBP_ID_2663531,Human_RBP_ID_5527837,Human_RBP_ID_9384058,Human_RBP_ID_18999684,Human_RBP_ID_24546296,Human_RBP_ID_26339460 Human_Splice_Rec_263925,Human_Splice_Rec_263985,Human_Splice_Rec_264047,Human_Splice_Rec_264111,Human_Splice_Rec_264159,Human_Splice_Rec_264211,Human_Splice_Rec_264265,Human_Splice_Rec_264325,Human_Splice_Rec_264369,Human_Splice_Rec_264417 RMVar_hsa_circ_7963,RMVar_hsa_circ_127386,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_201322,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_111366,RMVar_hsa_circ_126896,RMVar_hsa_circ_115995,RMVar_hsa_circ_201325,RMVar_hsa_circ_201327,RMVar_hsa_circ_201328,RMVar_hsa_circ_373000,RMVar_hsa_circ_201331 103644 RMVar_ID_103644 Human_SNP_ID_77859535 m1A Human chr2 + 74378183 74378183 74378183 GTGCCTCGGTGGCCTTTTCCAATCACCTCTACACGGGAGCCCACCCGCAGAGGCCGGGCGCTTGC GTGCCTCGGTGGCCTTTTCCAATCACCTCTACGCGGGAGCCCACCCGCAGAGGCCGGGCGCTTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74378055..74378250 26863196 MeRIP-seq:(Medium) rs774308744 Functional Loss SNV dbSNP153 33..33 33 - - - 103645 RMVar_ID_103645 Human_SNP_ID_77859570 m1A Human chr2 - 74378245 74378245 74378245 TCTAACTGTCTGTGTTTACCTGTGTCTTTCAGACGCCCAGCGGCAGCAGGATGAGTGCGGAGGCA TCTAACTGTCTGTGTTTACCTGTGTCTTTCAGGCGCCCAGCGGCAGCAGGATGAGTGCGGAGGCA T C DCTN1 Ensembl:ENSG00000204843 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74377659..74378942 26863196 MeRIP-seq:(Medium) rs1175904687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243274,Human_RBP_ID_922323,Human_RBP_ID_4622465,Human_RBP_ID_8851962 Human_Splice_Rec_263904,Human_Splice_Rec_263966,Human_Splice_Rec_264026,Human_Splice_Rec_264096,Human_Splice_Rec_264250,Human_Splice_Rec_264304,Human_Splice_Rec_264402,Human_Splice_Rec_264484,Human_Splice_Rec_264500,Human_Splice_Rec_264510,Human_Splice_Rec_264516,Human_Splice_Rec_264522,Human_Splice_Rec_264530,Human_Splice_Rec_264534,Human_Splice_Rec_264536 RMVar_hsa_circ_111366,RMVar_hsa_circ_201328,RMVar_hsa_circ_373000,RMVar_hsa_circ_201331,RMVar_hsa_circ_201335,RMVar_hsa_circ_327207 103646 RMVar_ID_103646 Human_SNP_ID_77859991 m1A Human chr2 - 74380053 74380053 74380053 CTCTGTCTTTGGCCAGCTGGGGGAGGGGGTAGAGGCCGGGTGAGCAACATGGCACAGAGCAAGAG CTCTGTCTTTGGCCAGCTGGGGGAGGGGGTAGGGGCCGGGTGAGCAACATGGCACAGAGCAAGAG T C DCTN1 Ensembl:ENSG00000204843 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74380048..74380191 32194978 MeRIP-seq:(Medium) rs754360623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_263903,Human_Splice_Rec_263965,Human_Splice_Rec_264025,Human_Splice_Rec_264401,Human_Splice_Rec_264519 RMVar_hsa_circ_111366,RMVar_hsa_circ_201328 103647 RMVar_ID_103647 Human_SNP_ID_77862949 m1A Human chr2 + 74391733 74391704 74391734 ACACCGGGCTCGGTCCCCAGCCCACCGCCGGCAACCTCACGAACACGTAGGGGGCCGGCGGAGCA ACAC______________________________CCTCACGAACACGTAGGGGGCCGGCGGAGCA CCGGGCTCGGTCCCCAGCCCACCGCCGGCAA C DCTN1-AS1 Ensembl:ENSG00000237737 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74391729..74391875 26863196 MeRIP-seq:(Medium) rs1558957659 Functional Loss DEL dbSNP153 5..34 33 - - - 103648 RMVar_ID_103648 Human_SNP_ID_77863008 m1A Human chr2 + 74391819 74391807 74391819 TCCGTACCTGCACTGTGAGGGGCTCCGCGCCCAGCTCCGACCCCACCGACGACCGACGCCCAAGA TCCGTACCTGCACTGTGAGGG____________GCTCCGACCCCACCGACGACCGACGCCCAAGA GGCTCCGCGCCCA G DCTN1-AS1 Ensembl:ENSG00000237737 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:74391791..74391961 26863196 MeRIP-seq:(Medium) rs1558957834 Functional Loss DEL dbSNP153 22..33 33 - - - 103649 RMVar_ID_103649 Human_SNP_ID_77863116 m1A Human chr2 + 74391952 74391952 74391952 ACCGCCCAGAACCCTTCGGCCCAGAGGCCCAGAGGCGTTCTGGGTCGAGTGAACCCTCTTTTCCC ACCGCCCAGAACCCTTCGGCCCAGAGGCCCAGGGGCGTTCTGGGTCGAGTGAACCCTCTTTTCCC A G DCTN1-AS1 Ensembl:ENSG00000237737 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74391911..74392008 26863196 MeRIP-seq:(Medium) rs1400256053 Functional Loss SNV dbSNP153 33..33 33 - - - 103650 RMVar_ID_103650 Human_SNP_ID_77868494 m1A Human chr2 - 74414573 74414573 74414573 GCCTCCACAGGGTCTGGAGCTGGCAGACAGGGAGGGCCAGGATCCTGGCAGATGGCCTCGAACCA GCCTCCACAGGGTCTGGAGCTGGCAGACAGGGCGGGCCAGGATCCTGGCAGATGGCCTCGAACCA T G C2orf81,AC005041.1 Ensembl:ENSG00000284308,Ensembl:ENSG00000159239 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:74414570..74414697 26863196 MeRIP-seq:(Medium) rs1019553119 Functional Loss SNV dbSNP153 33..33 33 - - - 103651 RMVar_ID_103651 Human_SNP_ID_77870851 m1A Human chr2 + 74422175 74422175 74422175 CCCCACACAGGATGTTCCGCTGGGAGCGCTCCATTCCCCTGCGAGGCTCGGCCGCCGCCCTGTGC CCCCACACAGGATGTTCCGCTGGGAGCGCTCCGTTCCCCTGCGAGGCTCGGCCGCCGCCCTGTGC A G WDR54 Ensembl:ENSG00000005448 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74422151..74422175 32194978 MeRIP-seq:(Medium) rs1189065413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4625457,Human_RBP_ID_13967267 Human_Splice_Rec_264644,Human_Splice_Rec_264646,Human_Splice_Rec_264650,Human_Splice_Rec_264656,Human_Splice_Rec_264686 RMVar_hsa_circ_100087,RMVar_hsa_circ_76531,RMVar_hsa_circ_107581,RMVar_hsa_circ_201338,RMVar_hsa_circ_201340,RMVar_hsa_circ_201341,RMVar_hsa_circ_201339 103652 RMVar_ID_103652 Human_SNP_ID_77871363 m1A Human chr2 - 74423728 74423728 74423728 TAACAAAACCCCCTCTCACTGCTCCAACGGCCATGCCCCTTCATTCACTAGCCTTGTCTTATCCC TAACAAAACCCCCTCTCACTGCTCCAACGGCCGTGCCCCTTCATTCACTAGCCTTGTCTTATCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74423548..74423790 26863196 MeRIP-seq:(Medium) rs765312968 Functional Loss SNV dbSNP153 33..33 33 - - - 103653 RMVar_ID_103653 Human_SNP_ID_77873921 m1A Human chr2 - 74432560 74432560 74432560 CTCCCAGCGAGAGCAGGCTCTGGAGGCCACCAAGAGCCTGCTAGTGTGCAACAGCCGCATCCTCA CTCCCAGCGAGAGCAGGCTCTGGAGGCCACCAGGAGCCTGCTAGTGTGCAACAGCCGCATCCTCA T C RTKN Ensembl:ENSG00000114993 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs371451515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_264743,Human_Splice_Rec_264767,Human_Splice_Rec_264789,Human_Splice_Rec_264822,Human_Splice_Rec_264823 RMVar_hsa_circ_90788,RMVar_hsa_circ_201352,RMVar_hsa_circ_323397 103654 RMVar_ID_103654 Human_SNP_ID_77875355 m1A Human chr2 + 74438674 74438674 74438674 TATATTCCAGCCACACTGGCTCTCTCTTTCCCACAAATATATTACCCTCATCCTCATATCAGGGC TATATTCCAGCCACACTGGCTCTCTCTTTCCCGCAAATATATTACCCTCATCCTCATATCAGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74438672..74438763 26863196 MeRIP-seq:(Medium) rs1323481218 Functional Loss SNV dbSNP153 33..33 33 - - - 103655 RMVar_ID_103655 Human_SNP_ID_77875796 m1A Human chr2 + 74440434 74440434 74440434 GCCTGTCTGCTGCTGTCCCCGCTCCCTTCTGCAGGCCCCTTCCCTTCCAGACAGGAAACCAGCCC GCCTGTCTGCTGCTGTCCCCGCTCCCTTCTGCTGGCCCCTTCCCTTCCAGACAGGAAACCAGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74440352..74440560 26863196 MeRIP-seq:(Medium) rs1204395371 Functional Loss SNV dbSNP153 33..33 33 - - - 103656 RMVar_ID_103656 Human_SNP_ID_77880409 m1A Human chr2 + 74457470 74457470 74457470 GCGCGAGGAGCGGGCGCGGAAGCGGCGGCTCCAGGCGGCGCGGCGGGCAGAAGAGCACAAGAACC GCGCGAGGAGCGGGCGCGGAAGCGGCGGCTCCGGGCGGCGCGGCGGGCAGAAGAGCACAAGAACC A G INO80B,INO80B-WBP1 Ensembl:ENSG00000115274,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74457427..74457530 26863196 MeRIP-seq:(Medium) rs1375758975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_264870,Human_Splice_Rec_264927 103657 RMVar_ID_103657 Human_SNP_ID_77880410 m1A Human chr2 + 74457470 74457470 74457470 GCGCGAGGAGCGGGCGCGGAAGCGGCGGCTCCAGGCGGCGCGGCGGGCAGAAGAGCACAAGAACC GCGCGAGGAGCGGGCGCGGAAGCGGCGGCTCCTGGCGGCGCGGCGGGCAGAAGAGCACAAGAACC A T INO80B,INO80B-WBP1 Ensembl:ENSG00000115274,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74457427..74457530 26863196 MeRIP-seq:(Medium) rs1375758975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_264870,Human_Splice_Rec_264927 103658 RMVar_ID_103658 Human_SNP_ID_77881531 m1A Human chr2 + 74460282 74460281 74460282 TACGAGGATGTGGTTCACCGCCCAGGCACACCACCCCCCCCTTATACTGTGGCCCCAGGCCGCCC TACGAGGATGTGGTTCACCGCCCAGGCACACC_CCCCCCCCTTATACTGTGGCCCCAGGCCGCCC CA C WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74460236..74460417 26863196 MeRIP-seq:(Medium) rs1433815904 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_555931,Human_RBP_ID_27481867,Human_RBP_ID_27564077 Human_Splice_Rec_264918,Human_Splice_Rec_264932,Human_Splice_Rec_264940,Human_Splice_Rec_264946,Human_Splice_Rec_264960,Human_Splice_Rec_264968,Human_Splice_Rec_264974,Human_Splice_Rec_264980,Human_Splice_Rec_264986,Human_Splice_Rec_264994,Human_Splice_Rec_265002,Human_Splice_Rec_265018 103659 RMVar_ID_103659 Human_SNP_ID_77881532 m1A Human chr2 + 74460282 74460282 74460282 TACGAGGATGTGGTTCACCGCCCAGGCACACCACCCCCCCCTTATACTGTGGCCCCAGGCCGCCC TACGAGGATGTGGTTCACCGCCCAGGCACACCCCCCCCCCCTTATACTGTGGCCCCAGGCCGCCC A C WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74460236..74460417 26863196 MeRIP-seq:(Medium) rs574091294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555931,Human_RBP_ID_27481867,Human_RBP_ID_27564077 Human_Splice_Rec_264918,Human_Splice_Rec_264932,Human_Splice_Rec_264940,Human_Splice_Rec_264946,Human_Splice_Rec_264960,Human_Splice_Rec_264968,Human_Splice_Rec_264974,Human_Splice_Rec_264980,Human_Splice_Rec_264986,Human_Splice_Rec_264994,Human_Splice_Rec_265002,Human_Splice_Rec_265018 103660 RMVar_ID_103660 Human_SNP_ID_77881533 m1A Human chr2 + 74460282 74460282 74460282 TACGAGGATGTGGTTCACCGCCCAGGCACACCACCCCCCCCTTATACTGTGGCCCCAGGCCGCCC TACGAGGATGTGGTTCACCGCCCAGGCACACCGCCCCCCCCTTATACTGTGGCCCCAGGCCGCCC A G WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74460236..74460417 26863196 MeRIP-seq:(Medium) rs574091294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555931,Human_RBP_ID_27481867,Human_RBP_ID_27564077 Human_Splice_Rec_264918,Human_Splice_Rec_264932,Human_Splice_Rec_264940,Human_Splice_Rec_264946,Human_Splice_Rec_264960,Human_Splice_Rec_264968,Human_Splice_Rec_264974,Human_Splice_Rec_264980,Human_Splice_Rec_264986,Human_Splice_Rec_264994,Human_Splice_Rec_265002,Human_Splice_Rec_265018 103661 RMVar_ID_103661 Human_SNP_ID_77881579 m1A Human chr2 + 74460354 74460354 74460354 GCTTCCAGTGAACAAACCTGCTGTTCCTCCTCATCCAGCTGCCCTGCCCACTTTGAAGGAACAAA GCTTCCAGTGAACAAACCTGCTGTTCCTCCTCTTCCAGCTGCCCTGCCCACTTTGAAGGAACAAA A T WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74460303..74460509 26863196 MeRIP-seq:(Medium) rs947864016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555933,Human_RBP_ID_4617051,Human_RBP_ID_17658497 Human_miRNA_ID_99962,Human_miRNA_ID_99963 103662 RMVar_ID_103662 Human_SNP_ID_77881600 m1A Human chr2 + 74460412 74460412 74460412 GAACAAATGTGGAAGGTGTTTCCTCCCACCAGAGTGCCCCCCCTCATCAGGAGGGTGAGCCCGGG GAACAAATGTGGAAGGTGTTTCCTCCCACCAGGGTGCCCCCCCTCATCAGGAGGGTGAGCCCGGG A G WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74460209..74460555 26863196 MeRIP-seq:(Medium) rs756065273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555935,Human_RBP_ID_777626,Human_RBP_ID_17658077 103663 RMVar_ID_103663 Human_SNP_ID_77882027 m1A Human chr2 + 74461476 74461476 74461476 TTGGCAGCCCGAGCCTGGTGAGGACCCTCCAGATGCCCATAGTGGTGGAGTGCTCCCAAAGCCAG TTGGCAGCCCGAGCCTGGTGAGGACCCTCCAGGTGCCCATAGTGGTGGAGTGCTCCCAAAGCCAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74461426..74461825 32194978 MeRIP-seq:(Medium) rs753884285 Functional Loss SNV dbSNP153 33..33 33 - - - 103664 RMVar_ID_103664 Human_SNP_ID_77882287 m1A Human chr2 - 74462124 74462124 74462124 TTTTCCTGGCTCCATCAGAGCCAGGCAGGCCCACTGCCACTATCTTACCGCTGGCGGGGACGGGA TTTTCCTGGCTCCATCAGAGCCAGGCAGGCCCCCTGCCACTATCTTACCGCTGGCGGGGACGGGA T G MOGS Ensembl:ENSG00000115275 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74462076..74462150 32194978 MeRIP-seq:(Medium) rs749913591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17965401,Human_RBP_ID_22765444 103665 RMVar_ID_103665 Human_SNP_ID_77882463 m1A Human chr2 - 74462565 74462565 74462565 CTCCTTGGTGGAATTGGCTACTTCTACGGACAAGGGCTGGTATTGCCAGACATCGGGGTGGAAGG CTCCTTGGTGGAATTGGCTACTTCTACGGACAGGGGCTGGTATTGCCAGACATCGGGGTGGAAGG T C MOGS Ensembl:ENSG00000115275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74462516..74462611 26863196 MeRIP-seq:(Medium) rs1194379910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_555963,Human_RBP_ID_1196992,Human_RBP_ID_1590547,Human_RBP_ID_8525605,Human_RBP_ID_13967410,Human_RBP_ID_17961598 103666 RMVar_ID_103666 Human_SNP_ID_77883312 m1A Human chr2 + 74464979 74464979 74464979 GGCGGTAGGTTCCCCAGAAGAGGTCCGGGGCCACGGCGGGGCTGGAGGAGTCGGCAGGCAACACA GGCGGTAGGTTCCCCAGAAGAGGTCCGGGGCCCCGGCGGGGCTGGAGGAGTCGGCAGGCAACACA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:74464926..74465150 26863410 MeRIP-seq:(Medium) rs1418910421 Functional Loss SNV dbSNP153 33..33 33 - - - 103667 RMVar_ID_103667 Human_SNP_ID_77885515 m1A Human chr2 + 74472177 74472177 74472177 TGTCCCCGCTGCCCGCCGCGTCCCTGGCCCGGATGTGGGAGGCGAAGGCGGTGAGCATTTCCAGA TGTCCCCGCTGCCCGCCGCGTCCCTGGCCCGGGTGTGGGAGGCGAAGGCGGTGAGCATTTCCAGA A G AC005041.5 Ensembl:ENSG00000286883 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74472126..74472689 26863196 MeRIP-seq:(Medium) rs750396824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_265120 103668 RMVar_ID_103668 Human_SNP_ID_77885543 m1A Human chr2 - 74472251 74472251 74472251 TCCCTGTCTCACTCGTTTGTTTCTTCCCCAGGAGACGGGCATCGCCTGATTATGCGCGGCGCTCA TCCCTGTCTCACTCGTTTGTTTCTTCCCCAGGCGACGGGCATCGCCTGATTATGCGCGGCGCTCA T G MRPL53,CCDC142 Ensembl:ENSG00000204822,Ensembl:ENSG00000135637 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74472206..74472306 32194978 MeRIP-seq:(Medium) rs777131002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243641,Human_RBP_ID_916415,Human_RBP_ID_22670134,Human_RBP_ID_25578003 Human_Splice_Rec_265124,Human_Splice_Rec_265126,Human_Splice_Rec_265128,Human_Splice_Rec_265150 103669 RMVar_ID_103669 Human_SNP_ID_77885745 m1A Human chr2 + 74472625 74472625 74472625 AAGGGACAGAACTGAACCCGAACCTGTTTGACAGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC AAGGGACAGAACTGAACCCGAACCTGTTTGACCGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC A C AC005041.5 Ensembl:ENSG00000286883 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:74472099..74472675;chr2:74472454..74472675;chr2:74472432..74472675 26863196 MeRIP-seq:(Medium) rs768630208 Functional Loss SNV dbSNP153 33..33 33 - - - 103670 RMVar_ID_103670 Human_SNP_ID_77885746 m1A Human chr2 + 74472625 74472625 74472625 AAGGGACAGAACTGAACCCGAACCTGTTTGACAGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC AAGGGACAGAACTGAACCCGAACCTGTTTGACGGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC A G AC005041.5 Ensembl:ENSG00000286883 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:74472099..74472675;chr2:74472454..74472675;chr2:74472432..74472675 26863196 MeRIP-seq:(Medium) rs768630208 Functional Loss SNV dbSNP153 33..33 33 - - - 103671 RMVar_ID_103671 Human_SNP_ID_77888542 m1A Human chr2 + 74481912 74481912 74481912 TTAGGTCCAGACTCTGAGCACAGGCTGCCCACAGCAGGGTCCAGTATTGGCTCCACAAGGCCCCA TTAGGTCCAGACTCTGAGCACAGGCTGCCCACGGCAGGGTCCAGTATTGGCTCCACAAGGCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74481862..74482093 26863196 MeRIP-seq:(Medium) rs1371102218 Functional Loss SNV dbSNP153 33..33 33 - - - 103672 RMVar_ID_103672 Human_SNP_ID_77889042 m1A Human chr2 - 74482932 74482932 74482932 TGAAGGTCCCCGCGACTCCCGGACTGGAGAAAACGGCTCTTGCGATGGGGCGAAGTCCGAGCTGC TGAAGGTCCCCGCGACTCCCGGACTGGAGAAATCGGCTCTTGCGATGGGGCGAAGTCCGAGCTGC T A CCDC142 Ensembl:ENSG00000135637 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74482547..74482980 26863196 MeRIP-seq:(Medium) rs903129139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422259 103673 RMVar_ID_103673 Human_SNP_ID_77889251 m1A Human chr2 - 74483342 74483342 74483342 AAGTTTGGGTGCAGCAGCGACCTCCAGTGGGCAGCTGGGCCGTAGAGAGCAGTCTACAGGAAAGG AAGTTTGGGTGCAGCAGCGACCTCCAGTGGGCGGCTGGGCCGTAGAGAGCAGTCTACAGGAAAGG T C CCDC142 Ensembl:ENSG00000135637 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74483338..74483716 26863196 MeRIP-seq:(Medium) rs202176729 Functional Loss SNV dbSNP153 33..33 33 - - - 103674 RMVar_ID_103674 Human_SNP_ID_77889285 m1A Human chr2 + 74483413 74483412 74483413 GAATTCGGTCCAGAGGATTACGGCGAAGAGGTAAAAGCGACCCTCAGTTTCCCCCAGTCCTGCTC GAATTCGGTCCAGAGGATTACGGCGAAGAGGT_AAAGCGACCCTCAGTTTCCCCCAGTCCTGCTC TA T TTC31 Ensembl:ENSG00000115282 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74483410..74483744 26863196 MeRIP-seq:(Medium) rs1558578180 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_19100753 Human_Splice_Rec_265214,Human_Splice_Rec_265226,Human_Splice_Rec_265250,Human_Splice_Rec_265272,Human_Splice_Rec_265286,Human_Splice_Rec_265308,Human_Splice_Rec_265322,Human_Splice_Rec_265340,Human_Splice_Rec_265342,Human_Splice_Rec_265354,Human_Splice_Rec_265366 RMVar_hsa_circ_108901,RMVar_hsa_circ_201362 103675 RMVar_ID_103675 Human_SNP_ID_77890941 m1A Human chr2 + 74490125 74490125 74490125 TGGGAGCAGCGGGCGGCTGCAGCTGTGGCACCATGGTGGGGAGTGCAGGGACCGGGCCCAGGGAT TGGGAGCAGCGGGCGGCTGCAGCTGTGGCACCGTGGTGGGGAGTGCAGGGACCGGGCCCAGGGAT A G TTC31 Ensembl:ENSG00000115282 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74490086..74490270 26863196 MeRIP-seq:(Medium) rs1429820232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9384080,Human_RBP_ID_19001928,Human_RBP_ID_19100754,Human_RBP_ID_22595703,Human_RBP_ID_22668457,Human_RBP_ID_23119295,Human_RBP_ID_26338597 Human_Splice_Rec_265217,Human_Splice_Rec_265229,Human_Splice_Rec_265289,Human_Splice_Rec_265311,Human_Splice_Rec_265325 RMVar_hsa_circ_108901,RMVar_hsa_circ_201362 103676 RMVar_ID_103676 Human_SNP_ID_77890943 m1A Human chr2 + 74490152 74490130 74490152 GCACCATGGTGGGGAGTGCAGGGACCGGGCCCAGGGATCGAGGCTGGTACCCTGGGAGGGCTGAC GCACCATGGTG______________________GGGATCGAGGCTGGTACCCTGGGAGGGCTGAC GGGGAGTGCAGGGACCGGGCCCA G TTC31 Ensembl:ENSG00000115282 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74490139..74490253 26863196 MeRIP-seq:(Medium) rs1444814224 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_918244,Human_RBP_ID_5379528,Human_RBP_ID_19001928,Human_RBP_ID_19100754,Human_RBP_ID_22417108,Human_RBP_ID_22547341,Human_RBP_ID_22595703,Human_RBP_ID_22668457,Human_RBP_ID_22742703,Human_RBP_ID_26787039 RMVar_hsa_circ_108901,RMVar_hsa_circ_201362 103677 RMVar_ID_103677 Human_SNP_ID_77890954 m1A Human chr2 + 74490152 74490152 74490152 GCACCATGGTGGGGAGTGCAGGGACCGGGCCCAGGGATCGAGGCTGGTACCCTGGGAGGGCTGAC GCACCATGGTGGGGAGTGCAGGGACCGGGCCCGGGGATCGAGGCTGGTACCCTGGGAGGGCTGAC A G TTC31 Ensembl:ENSG00000115282 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74490139..74490253 26863196 MeRIP-seq:(Medium) rs779350636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918244,Human_RBP_ID_5379528,Human_RBP_ID_19001928,Human_RBP_ID_19100754,Human_RBP_ID_22417108,Human_RBP_ID_22547341,Human_RBP_ID_22595703,Human_RBP_ID_22668457,Human_RBP_ID_22742703,Human_RBP_ID_26787039 RMVar_hsa_circ_108901,RMVar_hsa_circ_201362 103678 RMVar_ID_103678 Human_SNP_ID_77895765 m1A Human chr2 - 74507212 74507212 74507212 GCCGTCTAGTGTGATGAAGGAGGCGACCCCCAAGGTGGGAAGGCGCACGGGTTGGGGTTTGAGGG GCCGTCTAGTGTGATGAAGGAGGCGACCCCCACGGTGGGAAGGCGCACGGGTTGGGGTTTGAGGG T G PCGF1 Ensembl:ENSG00000115289 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74507082..74507638 26863196 MeRIP-seq:(Medium) rs1040271635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60843,Human_RBP_ID_4617279,Human_RBP_ID_22668461 103679 RMVar_ID_103679 Human_SNP_ID_77897874 m1A Human chr2 + 74514801 74514801 74514801 ACCACCGAACCTCCGGCGGTTCTCCTCGGCCCAGACCGATGGAGCCGGGGATGCTGGGTCCACAC ACCACCGAACCTCCGGCGGTTCTCCTCGGCCCCGACCGATGGAGCCGGGGATGCTGGGTCCACAC A C TLX2 Ensembl:ENSG00000115297 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74514697..74514807 32194978 MeRIP-seq:(Medium) rs1219357867 Functional Loss SNV dbSNP153 33..33 33 - - - 103680 RMVar_ID_103680 Human_SNP_ID_77898266 m1A Human chr2 + 74515806 74515806 74515806 ACCTGGCCTCTGCGGAGAGGGCGGCGCTGGCCAAGGCCTTGCGCATGACCGACGCACAGGTCAAA ACCTGGCCTCTGCGGAGAGGGCGGCGCTGGCCGAGGCCTTGCGCATGACCGACGCACAGGTCAAA A G TLX2 Ensembl:ENSG00000115297 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74515657..74516008 32194978 MeRIP-seq:(Medium) rs1377064161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_265477,Human_Splice_Rec_265483 103681 RMVar_ID_103681 Human_SNP_ID_77901529 m1A Human chr2 - 74526977 74526977 74526977 CAAGTCTTCCTGGGCCCGGCAGGAGAGCCTGCAGGAGCGCAAGCAAGCACTATATGAATACGCAA CAAGTCTTCCTGGGCCCGGCAGGAGAGCCTGCTGGAGCGCAAGCAAGCACTATATGAATACGCAA T A AUP1 Ensembl:ENSG00000115307 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74526676..74527095 26863196 MeRIP-seq:(Medium) rs1248363478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242456,Human_RBP_ID_775111,Human_RBP_ID_828447,Human_RBP_ID_3957977,Human_RBP_ID_9110859,Human_RBP_ID_17964059,Human_RBP_ID_18166756,Human_RBP_ID_22816274 Human_Splice_Rec_265593,Human_Splice_Rec_265612,Human_Splice_Rec_265613,Human_Splice_Rec_265634,Human_Splice_Rec_265635,Human_Splice_Rec_265655,Human_Splice_Rec_265661 Human_miRNA_ID_2842485 RMVar_hsa_circ_98500,RMVar_hsa_circ_123063,RMVar_hsa_circ_125197,RMVar_hsa_circ_115371,RMVar_hsa_circ_201374,RMVar_hsa_circ_201376,RMVar_hsa_circ_201377,RMVar_hsa_circ_201375 103682 RMVar_ID_103682 Human_SNP_ID_77901863 m1A Human chr2 + 74527869 74527869 74527869 AGCTAGGGAGAATTGGAAGACTGGAAGTGTCAAGATCTCAAGCTTTCCTCCCTCTCCTCCTAAGC AGCTAGGGAGAATTGGAAGACTGGAAGTGTCAGGATCTCAAGCTTTCCTCCCTCTCCTCCTAAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74527867..74527950 26863196 MeRIP-seq:(Medium) rs1338518572 Functional Loss SNV dbSNP153 33..33 33 - - - 103683 RMVar_ID_103683 Human_SNP_ID_77902511 m1A Human chr2 + 74529496 74529496 74529496 AGCAGCACGAGCAGTAGGAAGCAGTCACCCGGAAGCCTGGGGGCGAGAGGCGAAGTGGTCAGGCG AGCAGCACGAGCAGTAGGAAGCAGTCACCCGGGAGCCTGGGGGCGAGAGGCGAAGTGGTCAGGCG A G HTRA2 Ensembl:ENSG00000115317 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74529474..74529574 32194978 MeRIP-seq:(Medium) rs776448029 Functional Loss SNV dbSNP153 33..33 33 - - - 103684 RMVar_ID_103684 Human_SNP_ID_77902805 m1A Human chr2 - 74530074 74530073 74530074 CAGGGGTCAAACGGGGTCTCCTCCCCCAGCGAATGCCCCCCAAAGCCCGCCATGCCCGAAGGCTC CAGGGGTCAAACGGGGTCTCCTCCCCCAGCGA_TGCCCCCCAAAGCCCGCCATGCCCGAAGGCTC AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74529917..74530443 26863196 MeRIP-seq:(Medium) rs1019900133 Functional Loss DEL dbSNP153 33..33 33 - - - 103685 RMVar_ID_103685 Human_SNP_ID_77902806 m1A Human chr2 + 74530073 74530073 74530073 GGAGCCTTCGGGCATGGCGGGCTTTGGGGGGCATTCGCTGGGGGAGGAGACCCCGTTTGACCCCT GGAGCCTTCGGGCATGGCGGGCTTTGGGGGGCGTTCGCTGGGGGAGGAGACCCCGTTTGACCCCT A G HTRA2 Ensembl:ENSG00000115317 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74529917..74530474 26863196 MeRIP-seq:(Medium) rs1303491518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_917153,Human_RBP_ID_4622485,Human_RBP_ID_5379541,Human_RBP_ID_8942588,Human_RBP_ID_9330533,Human_RBP_ID_21980618,Human_RBP_ID_22077661,Human_RBP_ID_27817269 103686 RMVar_ID_103686 Human_SNP_ID_77902928 m1A Human chr2 - 74530326 74530326 74530326 GCACTGCCCCCCCAGCGCCCAGCGCCACCGCCAGCCACGCGCGCGAACGGGTTCCAGAGTTCTCT GCACTGCCCCCCCAGCGCCCAGCGCCACCGCCGGCCACGCGCGCGAACGGGTTCCAGAGTTCTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74530226..74530478 26863196 MeRIP-seq:(Medium) rs751421902 Functional Loss SNV dbSNP153 33..33 33 - - - 103687 RMVar_ID_103687 Human_SNP_ID_77903023 m1A Human chr2 + 74530509 74530509 74530509 AGCACCTGCCGTGGTCTATATCGAGATCCTGGACCGGTAATGGTGGGGGTAGACCGGGAGGCACT AGCACCTGCCGTGGTCTATATCGAGATCCTGGGCCGGTAATGGTGGGGGTAGACCGGGAGGCACT A G HTRA2 Ensembl:ENSG00000115317 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:74530409..74530508;chr2:74530163..74530508 32194978 MeRIP-seq:(Medium) rs746361219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_265673,Human_Splice_Rec_265688,Human_Splice_Rec_265689,Human_Splice_Rec_265704,Human_Splice_Rec_265705,Human_Splice_Rec_265729,Human_Splice_Rec_265739,Human_Splice_Rec_265751,Human_Splice_Rec_265763 103688 RMVar_ID_103688 Human_SNP_ID_77903428 m1A Human chr2 + 74531700 74531700 74531700 TCTTCGAGAGTTTCTGCATCGTGGGGAAAAGAAGAGTGAGCCTGCCTTATGGGGAAACGGGTTCC TCTTCGAGAGTTTCTGCATCGTGGGGAAAAGAGGAGTGAGCCTGCCTTATGGGGAAACGGGTTCC A G HTRA2 Ensembl:ENSG00000115317 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74531664..74531763 32194978 MeRIP-seq:(Medium) rs1558612606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19001983 Human_Splice_Rec_265681,Human_Splice_Rec_265697,Human_Splice_Rec_265713,Human_Splice_Rec_265727,Human_Splice_Rec_265735,Human_Splice_Rec_265747,Human_Splice_Rec_265757 103689 RMVar_ID_103689 Human_SNP_ID_77907752 m1A Human chr2 + 74549082 74549082 74549082 GAATCGCCCCCGCGCCTGGGAGTGGCCTCGCGAGGCCGGCGCGCGCCCCGGGGCCGAGGAATCCG GAATCGCCCCCGCGCCTGGGAGTGGCCTCGCGGGGCCGGCGCGCGCCCCGGGGCCGAGGAATCCG A G DOK1 Ensembl:ENSG00000115325 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74548993..74549283 26863196 MeRIP-seq:(Medium) rs1400529724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_265921,Human_Splice_Rec_265929 103690 RMVar_ID_103690 Human_SNP_ID_77908002 m1A Human chr2 + 74549857 74549857 74549857 CTGTGCCTGGAGCAGGAGGGAGCACTTCAAAAAGGAAATGGCTTTGAAGGAGGAGAAAGTCAGAA CTGTGCCTGGAGCAGGAGGGAGCACTTCAAAAGGGAAATGGCTTTGAAGGAGGAGAAAGTCAGAA A G DOK1 Ensembl:ENSG00000115325 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:74549808..74549922;chr2:74549808..74549920 26863196 MeRIP-seq:(Medium) rs1213525542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23885901 103691 RMVar_ID_103691 Human_SNP_ID_77908792 m1A Human chr2 + 74553008 74553004 74553008 GATGTGAGAGGAAGGGAGACTGTGGGAATGAGAGAGAGAAAACCAGAAAGACACAGAGGAGAGAG GATGTGAGAGGAAGGGAGACTGTGGGAAT____GAGAGAAAACCAGAAAGACACAGAGGAGAGAG TGAGA T DOK1 Ensembl:ENSG00000115325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74552639..74553891 26863196 MeRIP-seq:(Medium) rs1032521443 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_201387 103692 RMVar_ID_103692 Human_SNP_ID_77908793 m1A Human chr2 + 74553008 74553004 74553008 GATGTGAGAGGAAGGGAGACTGTGGGAATGAGAGAGAGAAAACCAGAAAGACACAGAGGAGAGAG GATGTGAGAGGAAGGGAGACTGTGGGAATGA__GAGAGAAAACCAGAAAGACACAGAGGAGAGAG TGAGA TGA DOK1 Ensembl:ENSG00000115325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74552639..74553891 26863196 MeRIP-seq:(Medium) rs1032521443 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_201387 103693 RMVar_ID_103693 Human_SNP_ID_77909559 m1A Human chr2 - 74555303 74555299 74555303 GGGGTCTCCACGGTGACGGGGGCCACACTCACACACTCAGCCAGACGGATCACTTTGCAGTCCAG GGGGTCTCCACGGTGACGGGGGCCACACTCAC____TCAGCCAGACGGATCACTTTGCAGTCCAG AGTGT A LOXL3 Ensembl:ENSG00000115318 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74555253..74555329 26863196 MeRIP-seq:(Medium) rs1451331635 Functional Loss DEL dbSNP153 33..36 33 - - - 103694 RMVar_ID_103694 Human_SNP_ID_77910016 m1A Human chr2 + 74556526 74556526 74556526 GAGGGGAAGTTGCCTTCCCCACCTGGCCCCCAAGAGCTCCTCGACAGTCCCCCAGCCCTGTATGC GAGGGGAAGTTGCCTTCCCCACCTGGCCCCCAGGAGCTCCTCGACAGTCCCCCAGCCCTGTATGC A G DOK1 Ensembl:ENSG00000115325 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74556475..74556567 26863196 MeRIP-seq:(Medium) rs770746152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27292639 103695 RMVar_ID_103695 Human_SNP_ID_77910206 m1A Human chr2 + 74556993 74556993 74556993 TGAACCTGGTACTGCAACTGGCAGTGGCATCAAAAGCCACAACTCAGCCCTGTACAGCCAGGTCC TGAACCTGGTACTGCAACTGGCAGTGGCATCAGAAGCCACAACTCAGCCCTGTACAGCCAGGTCC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1404094889 Functional Loss SNV dbSNP153 33..33 33 - - - 103696 RMVar_ID_103696 Human_SNP_ID_77910271 m1A Human chr2 + 74557175 74557173 74557176 GGGGACCATGGGGAGGTGGCACTAGGGATCAAAGAAGATGGTTAGAACCAGCAGAAGCCAGAGGG GGGGACCATGGGGAGGTGGCACTAGGGATCA___AAGATGGTTAGAACCAGCAGAAGCCAGAGGG AAAG A DOK1 Ensembl:ENSG00000115325 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74557125..74557306 26863196 MeRIP-seq:(Medium) rs1362268837 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5146840 103697 RMVar_ID_103697 Human_SNP_ID_77910286 m1A Human chr2 + 74557260 74557260 74557260 GAGACCAGGGGACCAGAGGGATGGGAGAGTCAAGGGAAGGACAATCCCAGGAAGTCCTAAGAAGT GAGACCAGGGGACCAGAGGGATGGGAGAGTCAGGGGAAGGACAATCCCAGGAAGTCCTAAGAAGT A G DOK1 Ensembl:ENSG00000115325 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74557046..74557372 26863196 MeRIP-seq:(Medium) rs1203572574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5146580,Human_RBP_ID_26486495 Human_miRNA_ID_544594,Human_miRNA_ID_579832,Human_miRNA_ID_655874 103698 RMVar_ID_103698 Human_SNP_ID_77932342 m1A Human chr2 - 74654428 74654428 74654428 CAGCACCGCCAGCAGCAGTAGCGGGAAGGGCGAGGCTGTAGGCTGCCCGGGACCCGGGCGGGGCC CAGCACCGCCAGCAGCAGTAGCGGGAAGGGCGGGGCTGTAGGCTGCCCGGGACCCGGGCGGGGCC T C lnc-M1AP-1 RNACentral:URS0000D5BE6E lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74654381..74654446 26863196 MeRIP-seq:(Medium) rs530989148 Functional Loss SNV dbSNP153 33..33 33 - - - 103699 RMVar_ID_103699 Human_SNP_ID_77975474 m1A Human chr2 + 74833830 74833830 74833830 CCACACCCCGGGTCCGCGATCACGCTCCCCCCACCCATAGCCGAGCCTGACGCGGCGGTGGCTCA CCACACCCCGGGTCCGCGATCACGCTCCCCCCCCCCATAGCCGAGCCTGACGCGGCGGTGGCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:74833690..74833987;chr2:74833781..74833873 26863196 MeRIP-seq:(Medium) rs954524860 Functional Loss SNV dbSNP153 33..33 33 - - - 103700 RMVar_ID_103700 Human_SNP_ID_77975647 m1A Human chr2 + 74834176 74834176 74834176 TCCGGCGCAGGAGTCCCGGGCTGCCGCTGGCAACATCGTGTCACCCAGCTAAGAAAATCCGCGGG TCCGGCGCAGGAGTCCCGGGCTGCCGCTGGCAGCATCGTGTCACCCAGCTAAGAAAATCCGCGGG A G HK2 Ensembl:ENSG00000159399 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74834126..74834243 26863196 MeRIP-seq:(Medium) rs978511835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8525702,Human_RBP_ID_26818657 103701 RMVar_ID_103701 Human_SNP_ID_77975763 m1A Human chr2 - 74834557 74834555 74834557 GGCAATCATCCTGCCGCGGCCCGACGGCGCAGAGTTGGGAAACCGAGGCGGAGACGCGAGAGGGG GGCAATCATCCTGCCGCGGCCCGACGGCGCAG__TTGGGAAACCGAGGCGGAGACGCGAGAGGGG ACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74834506..74835190 26863196 MeRIP-seq:(Medium) rs755688357 Functional Loss DEL dbSNP153 33..34 33 - - - 103702 RMVar_ID_103702 Human_SNP_ID_77988497 m1A Human chr2 + 74881803 74881803 74881803 GTGTTCGGAATGGGAAGTGGGGTGGAGTGGAGATGCACAACAAGATCTACGCCATCCCGCAGGAG GTGTTCGGAATGGGAAGTGGGGTGGAGTGGAGTTGCACAACAAGATCTACGCCATCCCGCAGGAG A T HK2 Ensembl:ENSG00000159399 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:74881752..74881817 26863196 MeRIP-seq:(Medium) rs371236382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22452324,Human_RBP_ID_23119441 Human_Splice_Rec_266254,Human_Splice_Rec_266255,Human_Splice_Rec_266288,Human_Splice_Rec_266289 RMVar_hsa_circ_123940,RMVar_hsa_circ_81517,RMVar_hsa_circ_98524,RMVar_hsa_circ_201394,RMVar_hsa_circ_201395,RMVar_hsa_circ_328878,RMVar_hsa_circ_117841,RMVar_hsa_circ_201396,RMVar_hsa_circ_201397 103703 RMVar_ID_103703 Human_SNP_ID_78007952 m1A Human chr2 + 74958704 74958704 74958704 AGGCCGGGATGGCGGCGGCGGCGGCGGCAGGAAGCGGGACGCCCCGAGAGGAGGAGGGACCTGCT AGGCCGGGATGGCGGCGGCGGCGGCGGCAGGACGCGGGACGCCCCGAGAGGAGGAGGGACCTGCT A C POLE4 Ensembl:ENSG00000115350 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:74958638..74959113;chr2:74958638..74958900 26863196 MeRIP-seq:(Medium) rs1441972660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828306,Human_RBP_ID_4622493,Human_RBP_ID_8942589,Human_RBP_ID_22997384 RMVar_hsa_circ_111016,RMVar_hsa_circ_201400 103704 RMVar_ID_103704 Human_SNP_ID_78007977 m1A Human chr2 + 74958726 74958726 74958726 GGCGGCAGGAAGCGGGACGCCCCGAGAGGAGGAGGGACCTGCTGGGGAGGCAGCGGCCTCGCAGC GGCGGCAGGAAGCGGGACGCCCCGAGAGGAGGGGGGACCTGCTGGGGAGGCAGCGGCCTCGCAGC A G POLE4 Ensembl:ENSG00000115350 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:74958676..74958862 26863196 MeRIP-seq:(Medium) rs1239085482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775126,Human_RBP_ID_828306,Human_RBP_ID_4622494,Human_RBP_ID_8942589,Human_RBP_ID_22997384 Human_miRNA_ID_2219750,Human_miRNA_ID_2256269,Human_miRNA_ID_2482790,Human_miRNA_ID_3071164 RMVar_hsa_circ_111016,RMVar_hsa_circ_201400 103705 RMVar_ID_103705 Human_SNP_ID_78008025 m1A Human chr2 + 74958797 74958797 74958797 CCCCAACGAGTGTGCCTGGGGCTCGTCTCTCGAGGTTGCCTCTGGCGCGAGTGAAGGCCTTGGTG CCCCAACGAGTGTGCCTGGGGCTCGTCTCTCGGGGTTGCCTCTGGCGCGAGTGAAGGCCTTGGTG A G POLE4 Ensembl:ENSG00000115350 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:74958686..74958883 32194978 MeRIP-seq:(Medium) rs751961431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4622495,Human_RBP_ID_5118304,Human_RBP_ID_8942590,Human_RBP_ID_9331068,Human_RBP_ID_9384097,Human_RBP_ID_22450414 Human_Splice_Rec_266321,Human_Splice_Rec_266327,Human_Splice_Rec_266331,Human_Splice_Rec_266337 RMVar_hsa_circ_111016,RMVar_hsa_circ_201400 103706 RMVar_ID_103706 Human_SNP_ID_78008273 m1A Human chr2 - 74959328 74959328 74959328 ATGGTCTCCACAAACAGTTCCTGTGAAGTAAAAAAGCAAAGTTTTAGTAATGGGTTCTAACACAC ATGGTCTCCACAAACAGTTCCTGTGAAGTAAATAAGCAAAGTTTTAGTAATGGGTTCTAACACAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:74959326..74959450;chr2:74959326..74959375 26863196 MeRIP-seq:(Medium) rs1191598397 Functional Loss SNV dbSNP153 33..33 33 - - - 103707 RMVar_ID_103707 Human_SNP_ID_614359092 m1A Human chr17 - 314784 314784 314784 CAATGGACGTGGAGTACAGGGACTACAGGTCAATGGAGGTGGGGTCACAGAGACTACAGGTCAAT CAATGGACGTGGAGTACAGGGACTACAGGTCAGTGGAGGTGGGGTCACAGAGACTACAGGTCAAT T C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:314735..314853 26863196 MeRIP-seq:(Medium) rs1555518479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3544620,Human_RBP_ID_5467328,Human_RBP_ID_8189047,Human_RBP_ID_9422139,Human_RBP_ID_18941080,Human_RBP_ID_23256818,Human_RBP_ID_24372002 RMVar_hsa_circ_180881,RMVar_hsa_circ_377774,RMVar_hsa_circ_180880,RMVar_hsa_circ_110895,RMVar_hsa_circ_358530,RMVar_hsa_circ_362663,RMVar_hsa_circ_180882,RMVar_hsa_circ_180884,RMVar_hsa_circ_73038,RMVar_hsa_circ_357643,RMVar_hsa_circ_361770,RMVar_hsa_circ_306560,RMVar_hsa_circ_180885,RMVar_hsa_circ_180883 103708 RMVar_ID_103708 Human_SNP_ID_614359096 m1A Human chr17 - 314790 314790 314790 ACAGGTCAATGGACGTGGAGTACAGGGACTACAGGTCAATGGAGGTGGGGTCACAGAGACTACAG ACAGGTCAATGGACGTGGAGTACAGGGACTACTGGTCAATGGAGGTGGGGTCACAGAGACTACAG T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:314743..314832 26863196 MeRIP-seq:(Medium) rs879245490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3544620,Human_RBP_ID_5467328,Human_RBP_ID_8189047,Human_RBP_ID_9422139,Human_RBP_ID_18941080,Human_RBP_ID_23256818,Human_RBP_ID_24372002 RMVar_hsa_circ_180881,RMVar_hsa_circ_377774,RMVar_hsa_circ_180880,RMVar_hsa_circ_110895,RMVar_hsa_circ_358530,RMVar_hsa_circ_362663,RMVar_hsa_circ_180882,RMVar_hsa_circ_180884,RMVar_hsa_circ_73038,RMVar_hsa_circ_357643,RMVar_hsa_circ_361770,RMVar_hsa_circ_306560,RMVar_hsa_circ_180885,RMVar_hsa_circ_180883 103709 RMVar_ID_103709 Human_SNP_ID_614380515 m1A Human chr17 - 380376 380333 380377 AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AAGCATGAGGAGGGCTTCCGGGAGGGATGAG__________________________________ TCTCATCCCTCCCGGAAGCCCTCCTCATGCTTCCCGGAAGCCCTC T RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:380313..380436 26863196 MeRIP-seq:(Medium) rs1567557884 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_21975249,Human_RBP_ID_22475469 103710 RMVar_ID_103710 Human_SNP_ID_614380516 m1A Human chr17 - 380335 380335 380335 GGGAAGCATGAGGAGGGCTTCCGGGAGGGATGAGAAGGGCTTCCGGGAGGCTGGTACTGCCTGGT GGGAAGCATGAGGAGGGCTTCCGGGAGGGATGTGAAGGGCTTCCGGGAGGCTGGTACTGCCTGGT T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:380333..380416 26863196 MeRIP-seq:(Medium) rs1278646128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542332,Human_RBP_ID_5143967,Human_RBP_ID_5318185,Human_RBP_ID_8189069,Human_RBP_ID_18941099,Human_RBP_ID_21973987,Human_RBP_ID_22474906 103711 RMVar_ID_103711 Human_SNP_ID_614380531 m1A Human chr17 - 380376 380351 380376 AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AAGCATGAGGAGGGCTTCCGGGAGGGATGAGG_________________________GCTTCCGG CCCTCCTCATGCTTCCCGGAAGCCCT C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:380313..380436 26863196 MeRIP-seq:(Medium) rs1465221206 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_21975249,Human_RBP_ID_22475469 103712 RMVar_ID_103712 Human_SNP_ID_614380546 m1A Human chr17 - 380376 380373 380376 AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AAGCATGAGGAGGGCTTCCGGGAGGGATGAGG___GCTTCCGGGAAGCATGAGGAGGGCTTCCGG CCCT C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:380313..380436 26863196 MeRIP-seq:(Medium) rs1316623627 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_21975249,Human_RBP_ID_22475469 103713 RMVar_ID_103713 Human_SNP_ID_614380548 m1A Human chr17 - 380376 380376 380376 AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGTGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:380313..380436 26863196 MeRIP-seq:(Medium) rs186675613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21975249,Human_RBP_ID_22475469 103714 RMVar_ID_103714 Human_SNP_ID_614380549 m1A Human chr17 - 380376 380376 380376 AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AAGCATGAGGAGGGCTTCCGGGAGGGATGAGGGGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG T C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:380313..380436 26863196 MeRIP-seq:(Medium) rs186675613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21975249,Human_RBP_ID_22475469 103715 RMVar_ID_103715 Human_SNP_ID_614380779 m1A Human chr17 - 380794 380794 380794 GGGAAGCATGAGGGGGGCTTCCGGGAGGGATGAGGACGGCTTCCGGGAGGGATGTGGAGGGCTTC GGGAAGCATGAGGGGGGCTTCCGGGAGGGATGTGGACGGCTTCCGGGAGGGATGTGGAGGGCTTC T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:380787..380858 26863196 MeRIP-seq:(Medium) rs1361008746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21973991 103716 RMVar_ID_103716 Human_SNP_ID_614380963 m1A Human chr17 - 381100 381100 381100 AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGACGGCTTCCGGGAGGGATGTGGAGGGCTTCCGG AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGTCGGCTTCCGGGAGGGATGTGGAGGGCTTCCGG T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:381063..381180 26863196 MeRIP-seq:(Medium) rs1224785979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189074,Human_RBP_ID_21973995,Human_RBP_ID_22475473 103717 RMVar_ID_103717 Human_SNP_ID_614380964 m1A Human chr17 - 381100 381100 381100 AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGACGGCTTCCGGGAGGGATGTGGAGGGCTTCCGG AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGGCGGCTTCCGGGAGGGATGTGGAGGGCTTCCGG T C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:381063..381180 26863196 MeRIP-seq:(Medium) rs1224785979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189074,Human_RBP_ID_21973995,Human_RBP_ID_22475473 103718 RMVar_ID_103718 Human_SNP_ID_614380966 m1A Human chr17 - 381103 381103 381103 GGGAGGGATGAGGAGGGCTTCCGGGAGGGATGAGGACGGCTTCCGGGAGGGATGTGGAGGGCTTC GGGAGGGATGAGGAGGGCTTCCGGGAGGGATGTGGACGGCTTCCGGGAGGGATGTGGAGGGCTTC T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:381069..381167;chr17:381061..381145 26863196 MeRIP-seq:(Medium) rs866293032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189074,Human_RBP_ID_21973995,Human_RBP_ID_22475473 103719 RMVar_ID_103719 Human_SNP_ID_614380977 m1A Human chr17 - 381125 381125 381125 GGGAGGCATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAGGGATGAGGACGGCTTC GGGAGGCATGAGGAGGGCTTCCGGGAGGGATGTGGAGGGCTTCCGGGAGGGATGAGGACGGCTTC T A RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:381022..381166 26863196 MeRIP-seq:(Medium) rs1468894199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189074,Human_RBP_ID_21973995 103720 RMVar_ID_103720 Human_SNP_ID_614381175 m1A Human chr17 - 381439 381439 381439 AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGAGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG AGGGATGAGGAGGGCTTCCGGGAGGGATGAGGGGGGCTTCCGGGAAGCATGAGGAGGGCTTCCGG T C RPH3AL Ensembl:ENSG00000181031 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:381415..381528 26863196 MeRIP-seq:(Medium) rs1388346245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189077,Human_RBP_ID_21973999,Human_RBP_ID_22475475 103721 RMVar_ID_103721 Human_SNP_ID_614390747 m1A Human chr17 - 413546 413546 413546 GATGCCCTTGAGGGCCTCGGGGTCGGGGTGGAAGCCCTTGAGGGCCTCGGGGTCGGGGTGGAAGC GATGCCCTTGAGGGCCTCGGGGTCGGGGTGGATGCCCTTGAGGGCCTCGGGGTCGGGGTGGAAGC T A AC141424.1 Ensembl:ENSG00000241525 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:413462..413567 26863410 MeRIP-seq:(Medium) rs782016145 Functional Loss SNV dbSNP153 33..33 33 - - - 103722 RMVar_ID_103722 Human_SNP_ID_614390884 m1A Human chr17 + 413792 413703 413793 ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACACTGACCCCGAGGCCCTCAAGGGCTTCCACCCC __________________________________TGACCCCGAGGCCCTCAAGGGCTTCCACCCC TTGACCCCGAGGCCCTCAAGGGCTTCCACCCCGACCCCAAGGCCCTCAAGGGCTTCCACCCCGACCCCAAGGCCCTCAAGGGTTTCCACAC T C17orf97 Ensembl:ENSG00000187624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:413672..414021 26863196 MeRIP-seq:(Medium) rs1555539984 Functional Loss DEL dbSNP153 1..34 33 - - - 103723 RMVar_ID_103723 Human_SNP_ID_614390949 m1A Human chr17 + 413792 413777 413792 ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACACTGACCCCGAGGCCCTCAAGGGCTTCCACCCC ACCCCGACCCCAAGGCCC_______________CTGACCCCGAGGCCCTCAAGGGCTTCCACCCC CTCAAGGGTTTCCACA C C17orf97 Ensembl:ENSG00000187624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:413672..414021 26863196 MeRIP-seq:(Medium) rs782479225 Functional Loss DEL dbSNP153 19..33 33 - - - 103724 RMVar_ID_103724 Human_SNP_ID_614390952 m1A Human chr17 + 413792 413792 413792 ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACACTGACCCCGAGGCCCTCAAGGGCTTCCACCCC ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACCCTGACCCCGAGGCCCTCAAGGGCTTCCACCCC A C C17orf97 Ensembl:ENSG00000187624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:413672..414021 26863196 MeRIP-seq:(Medium) rs782653538 Functional Loss SNV dbSNP153 33..33 33 - - - 103725 RMVar_ID_103725 Human_SNP_ID_614400198 m1A Human chr17 + 445828 445828 445828 AAAAAAAAAAAAGAATAAAATTGGGGCCTGCTATATTTACCTTACTTCCTTTGGTGGTAAGGGGT AAAAAAAAAAAAGAATAAAATTGGGGCCTGCTCTATTTACCTTACTTCCTTTGGTGGTAAGGGGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:445826..445925 32194978 MeRIP-seq:(Medium) rs371490163 Functional Loss SNV dbSNP153 33..33 33 - - - 103726 RMVar_ID_103726 Human_SNP_ID_614418796 m1A Human chr17 - 555194 555194 555194 AGTGTAACTGAAGCCTAGCAGGCAAGGTGGAAAGTGGCAAGACGGGGCCAGAAAGCTGGGCAGGA AGTGTAACTGAAGCCTAGCAGGCAAGGTGGAAGGTGGCAAGACGGGGCCAGAAAGCTGGGCAGGA T C VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:555181..555397 26863196 MeRIP-seq:(Medium) rs1372560509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24482,RMVar_hsa_circ_267135,RMVar_hsa_circ_105613,RMVar_hsa_circ_75254,RMVar_hsa_circ_180893,RMVar_hsa_circ_96213,RMVar_hsa_circ_25064,RMVar_hsa_circ_265426,RMVar_hsa_circ_68364,RMVar_hsa_circ_125907,RMVar_hsa_circ_180895,RMVar_hsa_circ_348015,RMVar_hsa_circ_319309,RMVar_hsa_circ_180897,RMVar_hsa_circ_44875,RMVar_hsa_circ_352775,RMVar_hsa_circ_180896 103727 RMVar_ID_103727 Human_SNP_ID_614421809 m1A Human chr17 - 565727 565727 565727 CACACAGGCCCAGTGACCGGGAGTAGGCCAGCAGGGGAGCCGTTGCGAGGCCCACTGACCGGGAG CACACAGGCCCAGTGACCGGGAGTAGGCCAGCGGGGGAGCCGTTGCGAGGCCCACTGACCGGGAG T C VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:565537..565844 26863196 MeRIP-seq:(Medium) rs1227474832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6914,RMVar_hsa_circ_24482,RMVar_hsa_circ_105613,RMVar_hsa_circ_180893,RMVar_hsa_circ_96213,RMVar_hsa_circ_25064,RMVar_hsa_circ_265426,RMVar_hsa_circ_92947,RMVar_hsa_circ_125907,RMVar_hsa_circ_180895,RMVar_hsa_circ_319309,RMVar_hsa_circ_180897,RMVar_hsa_circ_44875,RMVar_hsa_circ_352775,RMVar_hsa_circ_180896,RMVar_hsa_circ_68192,RMVar_hsa_circ_76634,RMVar_hsa_circ_21501,RMVar_hsa_circ_82629,RMVar_hsa_circ_180899,RMVar_hsa_circ_180900,RMVar_hsa_circ_325157,RMVar_hsa_circ_180902,RMVar_hsa_circ_69079 103728 RMVar_ID_103728 Human_SNP_ID_614432898 m1A Human chr17 - 601931 601931 601931 CAGATCAATGGGGAAAGCTATTGAATATGCTCAGAAAACACTTCTCTTTCTCATATCTACCTAAC CAGATCAATGGGGAAAGCTATTGAATATGCTCCGAAAACACTTCTCTTTCTCATATCTACCTAAC T G VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:601927..602120 26863196 MeRIP-seq:(Medium) rs754876224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6914,RMVar_hsa_circ_96213,RMVar_hsa_circ_25064,RMVar_hsa_circ_92947,RMVar_hsa_circ_125907,RMVar_hsa_circ_180895,RMVar_hsa_circ_319309,RMVar_hsa_circ_180897,RMVar_hsa_circ_352775,RMVar_hsa_circ_180896,RMVar_hsa_circ_68192,RMVar_hsa_circ_76634,RMVar_hsa_circ_29436,RMVar_hsa_circ_297553,RMVar_hsa_circ_180899,RMVar_hsa_circ_180900,RMVar_hsa_circ_69079,RMVar_hsa_circ_346340,RMVar_hsa_circ_368115,RMVar_hsa_circ_314692,RMVar_hsa_circ_19113,RMVar_hsa_circ_75136,RMVar_hsa_circ_61948,RMVar_hsa_circ_320873,RMVar_hsa_circ_180904,RMVar_hsa_circ_180905,RMVar_hsa_circ_351766,RMVar_hsa_circ_312060,RMVar_hsa_circ_319262,RMVar_hsa_circ_60401,RMVar_hsa_circ_180907 103729 RMVar_ID_103729 Human_SNP_ID_614441869 m1A Human chr17 - 633564 633564 633564 TGGAATAAGGTATAATTGTAACCACGCCACGGAAAAAACAGATTGTTTTGGGTCATGCCTATCCC TGGAATAAGGTATAATTGTAACCACGCCACGGGAAAAACAGATTGTTTTGGGTCATGCCTATCCC T C VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:633546..633631 26863410 MeRIP-seq:(Medium) rs1203161743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6914,RMVar_hsa_circ_25064,RMVar_hsa_circ_125907,RMVar_hsa_circ_180897,RMVar_hsa_circ_76634,RMVar_hsa_circ_297553,RMVar_hsa_circ_180900,RMVar_hsa_circ_75136,RMVar_hsa_circ_61948,RMVar_hsa_circ_312060,RMVar_hsa_circ_319262,RMVar_hsa_circ_180912,RMVar_hsa_circ_276787,RMVar_hsa_circ_329917,RMVar_hsa_circ_378804,RMVar_hsa_circ_337370,RMVar_hsa_circ_180914,RMVar_hsa_circ_180913,RMVar_hsa_circ_180911,RMVar_hsa_circ_349026,RMVar_hsa_circ_180917,RMVar_hsa_circ_267512 103730 RMVar_ID_103730 Human_SNP_ID_614445690 m1A Human chr17 + 646514 646469 646515 GCCTCCTAAGGGTCTTATCTTTTCTAATCCGTATCACGGACTGGAGACTGGCTCCCACACACATC __________________________________CACGGACTGGAGACTGGCTCCCACACACATC CCGCGTGGCCACTGCCTCCTAAGGGTCTTATCTTTTCTAATCCGTAT C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:646409..646565 26863196 MeRIP-seq:(Medium) rs1408110666 Functional Loss DEL dbSNP153 1..34 33 - - - 103731 RMVar_ID_103731 Human_SNP_ID_614449717 m1A Human chr17 - 659799 659799 659799 AGCAGTGAGGGCCTGAACAAGGAGTAGAGAGAAGGGATAGAGTCTTGAGATGAAGCAGAGGGAGA AGCAGTGAGGGCCTGAACAAGGAGTAGAGAGATGGGATAGAGTCTTGAGATGAAGCAGAGGGAGA T A VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:659797..659866 26863196 MeRIP-seq:(Medium) rs1020877170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6914,RMVar_hsa_circ_25064,RMVar_hsa_circ_125907,RMVar_hsa_circ_180897,RMVar_hsa_circ_297553,RMVar_hsa_circ_61948,RMVar_hsa_circ_319262,RMVar_hsa_circ_180912,RMVar_hsa_circ_276787,RMVar_hsa_circ_378804,RMVar_hsa_circ_337370,RMVar_hsa_circ_180914,RMVar_hsa_circ_180913,RMVar_hsa_circ_349026,RMVar_hsa_circ_180917,RMVar_hsa_circ_180921,RMVar_hsa_circ_274826,RMVar_hsa_circ_120624,RMVar_hsa_circ_267512,RMVar_hsa_circ_307035,RMVar_hsa_circ_180919,RMVar_hsa_circ_318465,RMVar_hsa_circ_180922,RMVar_hsa_circ_180920 103732 RMVar_ID_103732 Human_SNP_ID_614464840 m1A Human chr17 - 714709 714709 714709 CGGCGGGGGTCGGCAGGGGGCCGGGTGGCGGAATGATGGAGGAGGAGGAACTGGAGTTCGTGGAG CGGCGGGGGTCGGCAGGGGGCCGGGTGGCGGAGTGATGGAGGAGGAGGAACTGGAGTTCGTGGAG T C VPS53 Ensembl:ENSG00000141252 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:714444..714850;chr17:714389..714850;chr17:714662..714825 26863196 MeRIP-seq:(Medium) rs760031973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767025,Human_RBP_ID_3949863,Human_RBP_ID_5420343,Human_RBP_ID_9353354,Human_RBP_ID_9422705,Human_RBP_ID_18987494,Human_RBP_ID_22959150,Human_RBP_ID_26330960,Human_RBP_ID_27812127 Human_Splice_Rec_1756073,Human_Splice_Rec_1756115,Human_Splice_Rec_1756161,Human_Splice_Rec_1756199,Human_Splice_Rec_1756233,Human_Splice_Rec_1756269,Human_Splice_Rec_1756291,Human_Splice_Rec_1756359,Human_Splice_Rec_1756377 103733 RMVar_ID_103733 Human_SNP_ID_614464851 m1A Human chr17 - 714727 714727 714727 AGGCCTGAGTTGGGCTCGCGGCGGGGGTCGGCAGGGGGCCGGGTGGCGGAATGATGGAGGAGGAG AGGCCTGAGTTGGGCTCGCGGCGGGGGTCGGCTGGGGGCCGGGTGGCGGAATGATGGAGGAGGAG T A VPS53 Ensembl:ENSG00000141252 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:714579..714850 26863196 MeRIP-seq:(Medium) rs762650541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237879,Human_RBP_ID_767025,Human_RBP_ID_3949863,Human_RBP_ID_4465021,Human_RBP_ID_5420343,Human_RBP_ID_5525155,Human_RBP_ID_9353354,Human_RBP_ID_9422705,Human_RBP_ID_17669943,Human_RBP_ID_18987494,Human_RBP_ID_22959150,Human_RBP_ID_26330960 103734 RMVar_ID_103734 Human_SNP_ID_614464852 m1A Human chr17 - 714727 714727 714727 AGGCCTGAGTTGGGCTCGCGGCGGGGGTCGGCAGGGGGCCGGGTGGCGGAATGATGGAGGAGGAG AGGCCTGAGTTGGGCTCGCGGCGGGGGTCGGCGGGGGGCCGGGTGGCGGAATGATGGAGGAGGAG T C VPS53 Ensembl:ENSG00000141252 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:714579..714850 26863196 MeRIP-seq:(Medium) rs762650541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237879,Human_RBP_ID_767025,Human_RBP_ID_3949863,Human_RBP_ID_4465021,Human_RBP_ID_5420343,Human_RBP_ID_5525155,Human_RBP_ID_9353354,Human_RBP_ID_9422705,Human_RBP_ID_17669943,Human_RBP_ID_18987494,Human_RBP_ID_22959150,Human_RBP_ID_26330960 103735 RMVar_ID_103735 Human_SNP_ID_614470343 m1A Human chr17 + 732635 732635 732635 ACCCAGCCACGCGGCGCCAGCGAGGCGGCCGGACCCGCAGCCCCGATGCTGCTGACGCTGGCCGG ACCCAGCCACGCGGCGCCAGCGAGGCGGCCGGCCCCGCAGCCCCGATGCTGCTGACGCTGGCCGG A C TLCD3A Ensembl:ENSG00000167695 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr17:732303..732711;chr17:732461..732816 26863410,26863196 MeRIP-seq:(Medium) rs1323438044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445999,Human_RBP_ID_22443286 103736 RMVar_ID_103736 Human_SNP_ID_614470344 m1A Human chr17 + 732635 732635 732635 ACCCAGCCACGCGGCGCCAGCGAGGCGGCCGGACCCGCAGCCCCGATGCTGCTGACGCTGGCCGG ACCCAGCCACGCGGCGCCAGCGAGGCGGCCGGTCCCGCAGCCCCGATGCTGCTGACGCTGGCCGG A T TLCD3A Ensembl:ENSG00000167695 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr17:732303..732711;chr17:732461..732816 26863410,26863196 MeRIP-seq:(Medium) rs1323438044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4445999,Human_RBP_ID_22443286 103737 RMVar_ID_103737 Human_SNP_ID_614473068 m1A Human chr17 - 741284 741284 741284 TGTGCTGCTGCTTTAGCTGCAATAGAAGAGGAAGGAAAAAGGTAAGGTCACCAAGAAGCTGGGCA TGTGCTGCTGCTTTAGCTGCAATAGAAGAGGAGGGAAAAAGGTAAGGTCACCAAGAAGCTGGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:741281..741361 26863196 MeRIP-seq:(Medium) rs1224754675 Functional Loss SNV dbSNP153 33..33 33 - - - 103738 RMVar_ID_103738 Human_SNP_ID_614474329 m1A Human chr17 + 745453 745453 745453 CTGGTGAAGGCGCTGCCACTCCTGAGGGCTGCACCAAGGCATGACTTGCACCAGGGCCACCAGAA CTGGTGAAGGCGCTGCCACTCCTGAGGGCTGCGCCAAGGCATGACTTGCACCAGGGCCACCAGAA A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:745404..745604 32194978 MeRIP-seq:(Medium) rs541236838 Functional Loss SNV dbSNP153 33..33 33 - - - 103739 RMVar_ID_103739 Human_SNP_ID_614474383 m1A Human chr17 - 745567 745567 745567 TCCTGGCCTGGATGGAGTGCTGCTGCGTCTCCAGCGGCATCTCGGAGAGGATGCTGTCTCTCTTG TCCTGGCCTGGATGGAGTGCTGCTGCGTCTCCGGCGGCATCTCGGAGAGGATGCTGTCTCTCTTG T C GEMIN4 Ensembl:ENSG00000179409 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:745516..745618 26863196 MeRIP-seq:(Medium) rs756746128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26969277 RMVar_hsa_circ_180931,RMVar_hsa_circ_97090,RMVar_hsa_circ_180930 103740 RMVar_ID_103740 Human_SNP_ID_614474897 m1A Human chr17 + 746752 746752 746752 CAGGCAGGCTACCCACTCGTCCGAGAAGGCCCACTTCTTCTCAGAGGCAAAAATGTAGCACACTT CAGGCAGGCTACCCACTCGTCCGAGAAGGCCCTCTTCTTCTCAGAGGCAAAAATGTAGCACACTT A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr17:746701..746868;chr17:746651..746850 26863196,26863410 MeRIP-seq:(Medium) rs1567777895 Functional Loss SNV dbSNP153 33..33 33 - - - 103741 RMVar_ID_103741 Human_SNP_ID_614475402 m1A Human chr17 - 747724 747724 747724 TGTTCTTCTCGGTGGGCAACATGATCCCCACCATCAACCACACCATCCTCTTCGAGCTGCTCAAA TGTTCTTCTCGGTGGGCAACATGATCCCCACCGTCAACCACACCATCCTCTTCGAGCTGCTCAAA T C GEMIN4 Ensembl:ENSG00000179409 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:747676..747725 32194978 MeRIP-seq:(Medium) rs746986265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5497595,Human_RBP_ID_5525159,Human_RBP_ID_17377289,Human_RBP_ID_17899463,Human_RBP_ID_18439537,Human_RBP_ID_22058884 Human_miRNA_ID_1957518,Human_miRNA_ID_2467262 RMVar_hsa_circ_180931,RMVar_hsa_circ_97090,RMVar_hsa_circ_180930 103742 RMVar_ID_103742 Human_SNP_ID_614476805 m1A Human chr17 - 752181 752181 752181 CGTCCCGCGCCGCGTTCGAGTTCTCGGAGGGGAGGGGGCGTTAGCCCCGCGCAGCCGCCGGCGTC CGTCCCGCGCCGCGTTCGAGTTCTCGGAGGGGGGGGGGCGTTAGCCCCGCGCAGCCGCCGGCGTC T C GEMIN4 Ensembl:ENSG00000179409 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:752053..752225 26863196 MeRIP-seq:(Medium) rs502853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822326,Human_RBP_ID_4465024,Human_RBP_ID_9326401 Human_Splice_Rec_1756411,Human_Splice_Rec_1756413,Human_Splice_Rec_1756417 RMVar_hsa_circ_97090,RMVar_hsa_circ_180930 103743 RMVar_ID_103743 Human_SNP_ID_614484847 m1A Human chr17 + 778669 778669 778669 TCTGTTATCCGGGTGTAGTCAGAGCCTAAAGGAGATTTTAAGAAACAAGGTATCATACCCATTAC TCTGTTATCCGGGTGTAGTCAGAGCCTAAAGGGGATTTTAAGAAACAAGGTATCATACCCATTAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:778667..778768 32194978 MeRIP-seq:(Medium) rs1442824322 Functional Loss SNV dbSNP153 33..33 33 - - - 103744 RMVar_ID_103744 Human_SNP_ID_614485987 m1A Human chr17 + 782238 782238 782238 AAGCGGTTTCCCACTTTGAATACGAAGTGCAGAGCTCTGCGAGCAGCCATGATTCCCGCCGCACG AAGCGGTTTCCCACTTTGAATACGAAGTGCAGCGCTCTGCGAGCAGCCATGATTCCCGCCGCACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:782051..782300 26863196 MeRIP-seq:(Medium) rs139319238 Functional Loss SNV dbSNP153 33..33 33 - - - 103745 RMVar_ID_103745 Human_SNP_ID_614485988 m1A Human chr17 + 782238 782238 782238 AAGCGGTTTCCCACTTTGAATACGAAGTGCAGAGCTCTGCGAGCAGCCATGATTCCCGCCGCACG AAGCGGTTTCCCACTTTGAATACGAAGTGCAGTGCTCTGCGAGCAGCCATGATTCCCGCCGCACG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:782051..782300 26863196 MeRIP-seq:(Medium) rs139319238 Functional Loss SNV dbSNP153 33..33 33 - - - 103746 RMVar_ID_103746 Human_SNP_ID_614485992 m1A Human chr17 - 782243 782243 782243 GGCTGCGTGCGGCGGGAATCATGGCTGCTCGCAGAGCTCTGCACTTCGTATTCAAAGTGGGAAAC GGCTGCGTGCGGCGGGAATCATGGCTGCTCGCGGAGCTCTGCACTTCGTATTCAAAGTGGGAAAC T C GLOD4 Ensembl:ENSG00000167699 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:782035..782275 26863196 MeRIP-seq:(Medium) rs756472020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498561,Human_RBP_ID_1183980,Human_RBP_ID_1541231,Human_RBP_ID_4465026,Human_RBP_ID_8461951,Human_RBP_ID_23746795 Human_Splice_Rec_1756431,Human_Splice_Rec_1756447,Human_Splice_Rec_1756475,Human_Splice_Rec_1756493,Human_Splice_Rec_1756505,Human_Splice_Rec_1756537,Human_Splice_Rec_1756553,Human_Splice_Rec_1756565,Human_Splice_Rec_1756577,Human_Splice_Rec_1756589,Human_Splice_Rec_1756601,Human_Splice_Rec_1756603,Human_Splice_Rec_1756605,Human_Splice_Rec_1756607 RMVar_hsa_circ_82792,RMVar_hsa_circ_180935,RMVar_hsa_circ_180937 103747 RMVar_ID_103747 Human_SNP_ID_614486148 m1A Human chr17 - 782410 782410 782410 AAGCCTGGACCACCTGCAGCAACGGTCGCACGACAAACCTCGCGGGTCTCACCAGCGCCGCCATG AAGCCTGGACCACCTGCAGCAACGGTCGCACGGCAAACCTCGCGGGTCTCACCAGCGCCGCCATG T C GLOD4 Ensembl:ENSG00000167699 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:782371..782522 26863196 MeRIP-seq:(Medium) rs773447599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82792,RMVar_hsa_circ_180935,RMVar_hsa_circ_180937 103748 RMVar_ID_103748 Human_SNP_ID_614488988 m1A Human chr17 + 791774 791774 791774 AGTGATGAAGTTTCACAAGTATGAGGAAGAGGAAGATGTAGAAACCGGAGCCAGTCAAGATTGGC AGTGATGAAGTTTCACAAGTATGAGGAAGAGGCAGATGTAGAAACCGGAGCCAGTCAAGATTGGC A C MRM3 Ensembl:ENSG00000171861 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:791688..791828 26863196 MeRIP-seq:(Medium) rs748868562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6640929,Human_RBP_ID_13151176,Human_RBP_ID_23746912 Human_miRNA_ID_1392039,Human_miRNA_ID_2084060 RMVar_hsa_circ_180938,RMVar_hsa_circ_103142,RMVar_hsa_circ_359598,RMVar_hsa_circ_113553,RMVar_hsa_circ_180940 103749 RMVar_ID_103749 Human_SNP_ID_614491848 m1A Human chr17 - 799967 799967 799967 GGATTACAGGCACCCGCCACCGTACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCAC GGATTACAGGCACCCGCCACCGTACCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCAC T C NXN Ensembl:ENSG00000167693 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs538435 Functional Loss SNV dbSNP153 33..33 33 - - - 103750 RMVar_ID_103750 Human_SNP_ID_614491996 m1A Human chr17 - 800559 800559 800559 TCTGACGTCGGCACACACGGCCCCGGACGGCCAGAGGGGAACCGCCGGGTGACACCTGCGTGGAG TCTGACGTCGGCACACACGGCCCCGGACGGCCGGAGGGGAACCGCCGGGTGACACCTGCGTGGAG T C NXN Ensembl:ENSG00000167693 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:800508..800808 32194978 MeRIP-seq:(Medium) rs1313216812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27258929 103751 RMVar_ID_103751 Human_SNP_ID_614501399 m1A Human chr17 + 826077 826077 826077 TGTTGGAAATTCGGTATTTGTTCCAAAGTTTGAGCTGTATGAAGAAAAGCAAAAGAAGGTGGTTA TGTTGGAAATTCGGTATTTGTTCCAAAGTTTGGGCTGTATGAAGAAAAGCAAAAGAAGGTGGTTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:826052..826136;chr17:826033..863941 26863196,32194978 MeRIP-seq:(Medium) rs763428527 Functional Loss SNV dbSNP153 33..33 33 - - - 103752 RMVar_ID_103752 Human_SNP_ID_614506386 m1A Human chr17 + 841413 841375 841414 TGCATCTCACGCCGGCGAGCAGGTCCCCCCTGACCACGGCGCATCTCACACGGGCGAGCAGGTCC __________________________________CACGGCGCATCTCACACGGGCGAGCAGGTCC ACACGGTGCATCTCACGCCGGCGAGCAGGTCCCCCCTGAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:841404..841513 26863196 MeRIP-seq:(Medium) rs1567827273 Functional Loss DEL dbSNP153 1..34 33 - - - 103753 RMVar_ID_103753 Human_SNP_ID_614506399 m1A Human chr17 + 841413 841389 841414 TGCATCTCACGCCGGCGAGCAGGTCCCCCCTGACCACGGCGCATCTCACACGGGCGAGCAGGTCC TGCATCTCA_________________________CACGGCGCATCTCACACGGGCGAGCAGGTCC ACGCCGGCGAGCAGGTCCCCCCTGAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:841404..841513 26863196 MeRIP-seq:(Medium) rs1302939739 Functional Loss DEL dbSNP153 10..34 33 - - - 103754 RMVar_ID_103754 Human_SNP_ID_614506491 m1A Human chr17 + 841440 841440 841440 CCCTGACCACGGCGCATCTCACACGGGCGAGCAGGTCCCCCTGACCACGGCGCATCTCACACGGG CCCTGACCACGGCGCATCTCACACGGGCGAGCGGGTCCCCCTGACCACGGCGCATCTCACACGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:841434..841575 26863196 MeRIP-seq:(Medium) rs1198722647 Functional Loss SNV dbSNP153 33..33 33 - - - 103755 RMVar_ID_103755 Human_SNP_ID_614522227 m1A Human chr17 + 891771 891771 891771 GCACAGCCCATCAGGGAACCTAAGCTAACCCCACCATGCAGAACCCAACAGGGAACCTAAACTAA GCACAGCCCATCAGGGAACCTAAGCTAACCCCGCCATGCAGAACCCAACAGGGAACCTAAACTAA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:891768..891897 26863196 MeRIP-seq:(Medium) rs1437386525 Functional Loss SNV dbSNP153 33..33 33 - - - 103756 RMVar_ID_103756 Human_SNP_ID_614531297 m1A Human chr17 - 920478 920478 920478 GGTGAGGGCTGGTCACTTGGGGAGGGAGCGGAACCCTGGGAGGAGAACGCTGGAGGAATTGGGAT GGTGAGGGCTGGTCACTTGGGGAGGGAGCGGAGCCCTGGGAGGAGAACGCTGGAGGAATTGGGAT T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:920476..920562 26863196 MeRIP-seq:(Medium) rs771789178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143978,Human_RBP_ID_5467467,Human_RBP_ID_8189095,Human_RBP_ID_22717316 103757 RMVar_ID_103757 Human_SNP_ID_614531691 m1A Human chr17 - 921802 921802 921802 CTGCCAGGTGTTGTCCAGGGGCAGTGAGGATGAGAGCCTGGGCCGGCCAGGTGTTGTCCAGGGGC CTGCCAGGTGTTGTCCAGGGGCAGTGAGGATGGGAGCCTGGGCCGGCCAGGTGTTGTCCAGGGGC T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:921800..921999 26863196 MeRIP-seq:(Medium) rs1317892627 Functional Loss SNV dbSNP153 33..33 33 - - - 103758 RMVar_ID_103758 Human_SNP_ID_614540365 m1A Human chr17 - 949034 949034 949034 GGAGAGGAGGAGGCAGGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGGAGCCCGGGGGGAGAGGAG GGAGAGGAGGAGGCAGGGGGAGAGGAGGAGGCCGGGGGGAGAGGAGGAGCCCGGGGGGAGAGGAG T G NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:949028..949099 26863196 MeRIP-seq:(Medium) rs371441941 Functional Loss SNV dbSNP153 33..33 33 - - - 103759 RMVar_ID_103759 Human_SNP_ID_614540476 m1A Human chr17 - 949659 949564 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCA_________________________________ CTGCCTCCTCCTCTCCCCGCGGCCTCCTCCTCTCCCCCCTGCCTCCTCCTCTCCCCGCGGCCTCCTCCTCTCCCCCCTGCCTCCTCCTCTCCCCGT C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs1567515406 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_8189100 103760 RMVar_ID_103760 Human_SNP_ID_614540504 m1A Human chr17 - 949659 949640 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCA___________________GGGGGGAGAGGAGG CTGCCTCCTCCTCTCCCCGT C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs1567515443 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_8189100 103761 RMVar_ID_103761 Human_SNP_ID_614540505 m1A Human chr17 - 949641 949641 949641 GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCTGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG T A NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:949636..949914 26863196 MeRIP-seq:(Medium) rs71358518 Functional Loss SNV dbSNP153 33..33 33 - - - 103762 RMVar_ID_103762 Human_SNP_ID_614540506 m1A Human chr17 - 949641 949641 949641 GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCGGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:949636..949914 26863196 MeRIP-seq:(Medium) rs71358518 Functional Loss SNV dbSNP153 33..33 33 - - - 103763 RMVar_ID_103763 Human_SNP_ID_614540507 m1A Human chr17 - 949641 949641 949641 GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG GAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCCGGGGGGAGAGGAGGAGGCCGCGGGGAGAGGAG T G NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:949636..949914 26863196 MeRIP-seq:(Medium) rs71358518 Functional Loss SNV dbSNP153 33..33 33 - - - 103764 RMVar_ID_103764 Human_SNP_ID_614540517 m1A Human chr17 - 949659 949657 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCA__GGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG CGT C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs1567515472 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8189100 103765 RMVar_ID_103765 Human_SNP_ID_614540521 m1A Human chr17 - 949659 949658 949660 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGC__CGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG GTT G NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs1290014770 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8189100 103766 RMVar_ID_103766 Human_SNP_ID_614540522 m1A Human chr17 - 949659 949658 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCA_CGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG GT G NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs1567515476 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8189100 103767 RMVar_ID_103767 Human_SNP_ID_614540527 m1A Human chr17 - 949659 949659 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCATCGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG T A NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs191975216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189100 103768 RMVar_ID_103768 Human_SNP_ID_614540528 m1A Human chr17 - 949659 949659 949659 AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAACGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG AGAGGAGGAGGCCACGGGGAGAGGAGGAGGCAGCGGGGAGAGGAGGAGGCAGGGGGGAGAGGAGG T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:949653..949935 26863196 MeRIP-seq:(Medium) rs191975216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189100 103769 RMVar_ID_103769 Human_SNP_ID_614540742 m1A Human chr17 - 950279 950279 950279 TCCCCCACCGAATCCCTTTCTTGTATAAAAAGATTCTGAAATTCTTCCTTGATTCTTTCCTGCCT TCCCCCACCGAATCCCTTTCTTGTATAAAAAGGTTCTGAAATTCTTCCTTGATTCTTTCCTGCCT T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:950274..950389 26863196 MeRIP-seq:(Medium) rs1293703776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18942609 103770 RMVar_ID_103770 Human_SNP_ID_614541576 m1A Human chr17 - 952715 952715 952715 GTGTGACCGTCCGTGGTACCTGCCGGGTTCCAACCTTGGTCTGTCTGACTCCAGCCCCCCCACAG GTGTGACCGTCCGTGGTACCTGCCGGGTTCCACCCTTGGTCTGTCTGACTCCAGCCCCCCCACAG T G NXN Ensembl:ENSG00000167693 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:952657..952811 26863196 MeRIP-seq:(Medium) rs1364498429 Functional Loss SNV dbSNP153 33..33 33 - - - 103771 RMVar_ID_103771 Human_SNP_ID_614543388 m1A Human chr17 + 957976 957976 957976 GGGAACCTCTGTTTTCCTCACAGAACGTGAAAATGTTTCCACGGAGCACGGGCAGCCCCCATCAC GGGAACCTCTGTTTTCCTCACAGAACGTGAAAGTGTTTCCACGGAGCACGGGCAGCCCCCATCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:957974..958184 26863196 MeRIP-seq:(Medium) rs1034036230 Functional Loss SNV dbSNP153 33..33 33 - - - 103772 RMVar_ID_103772 Human_SNP_ID_614555523 m1A Human chr17 + 997231 997231 997231 CGAAGCTCCGCTGCAGTACAGCCTGCTCCTGCAGTACCTGGTGGGTGACAAGCGTCAGCCCCGGC CGAAGCTCCGCTGCAGTACAGCCTGCTCCTGCGGTACCTGGTGGGTGACAAGCGTCAGCCCCGGC A G TIMM22 Ensembl:ENSG00000177370 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:997181..997328 26863196 MeRIP-seq:(Medium) rs368792625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546590,Human_RBP_ID_4465028,Human_RBP_ID_5365833,Human_RBP_ID_18713518 103773 RMVar_ID_103773 Human_SNP_ID_614555535 m1A Human chr17 - 997253 997253 997253 CCCAGGCTCCCAGGCTCCAGGAGCCGGGGCTGACGCTTGTCACCCACCAGGTACTGCAGGAGCAG CCCAGGCTCCCAGGCTCCAGGAGCCGGGGCTGTCGCTTGTCACCCACCAGGTACTGCAGGAGCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:997151..997300 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 103774 RMVar_ID_103774 Human_SNP_ID_614557111 m1A Human chr17 + 1002003 1002003 1002003 TCCTGCTGTGGTCATCTTGGTGACTCGGTCACAGCAGCTACTGGCCAAGATCAGACGTCGCTGAG TCCTGCTGTGGTCATCTTGGTGACTCGGTCACCGCAGCTACTGGCCAAGATCAGACGTCGCTGAG A C TIMM22 Ensembl:ENSG00000177370 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1001952..1002024 26863196 MeRIP-seq:(Medium) rs1229109361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504297,Human_RBP_ID_13218595,Human_RBP_ID_17904015,Human_RBP_ID_27459999,Human_RBP_ID_27561636 103775 RMVar_ID_103775 Human_SNP_ID_614557994 m1A Human chr17 + 1005060 1005060 1005060 GAAAAGCCCCCACAACTTGCTCCTAAGAGCTGAGCTGCCTCCCCGCGACCCGGGACACCCAGCGT GAAAAGCCCCCACAACTTGCTCCTAAGAGCTGGGCTGCCTCCCCGCGACCCGGGACACCCAGCGT A G lnc-TIMM22-2 RNACentral:URS00008B34B6 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1005010..1005163 26863196 MeRIP-seq:(Medium) rs1319454276 Functional Loss SNV dbSNP153 33..33 33 - - - 103776 RMVar_ID_103776 Human_SNP_ID_614558665 m1A Human chr17 - 1007252 1007252 1007252 ATGTCACTTCACAACCTGGCTACCGTGTTTGGACCCACGTTACTGAGACCCTCAGAAGTGGAGAG ATGTCACTTCACAACCTGGCTACCGTGTTTGGGCCCACGTTACTGAGACCCTCAGAAGTGGAGAG T C ABR Ensembl:ENSG00000159842 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1007202..1007303 32194978 MeRIP-seq:(Medium) rs776341273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1756758,Human_Splice_Rec_1756759,Human_Splice_Rec_1756766,Human_Splice_Rec_1756767,Human_Splice_Rec_1756810,Human_Splice_Rec_1756811,Human_Splice_Rec_1756826,Human_Splice_Rec_1756827,Human_Splice_Rec_1756868,Human_Splice_Rec_1756869,Human_Splice_Rec_1756910,Human_Splice_Rec_1756911,Human_Splice_Rec_1756924,Human_Splice_Rec_1756925,Human_Splice_Rec_1756958,Human_Splice_Rec_1756959,Human_Splice_Rec_1756966,Human_Splice_Rec_1756967,Human_Splice_Rec_1756972,Human_Splice_Rec_1756974 RMVar_hsa_circ_91339,RMVar_hsa_circ_180950 103777 RMVar_ID_103777 Human_SNP_ID_614560057 m1A Human chr17 + 1011956 1011956 1011956 CCCTCTTCTCCACCTCCTCCACACACTGCCGGACGATGTAGGGCACCTTGGAGCGCTCCCGCCTG CCCTCTTCTCCACCTCCTCCACACACTGCCGGGCGATGTAGGGCACCTTGGAGCGCTCCCGCCTG A G lnc-TIMM22-2 RNACentral:URS00008B34B6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1011905..1012018 26863196 MeRIP-seq:(Medium) rs754712200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5442130,Human_RBP_ID_13218784 103778 RMVar_ID_103778 Human_SNP_ID_614564298 m1A Human chr17 + 1023087 1023087 1023087 TCCGCTCCAGCGCCTCTGCCGGCCCCACGTCCACTGCAGAGCCTCTGCCGGCCCCACGTCCACTA TCCGCTCCAGCGCCTCTGCCGGCCCCACGTCCGCTGCAGAGCCTCTGCCGGCCCCACGTCCACTA A G lnc-TIMM22-2 RNACentral:URS00008B34B6 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1022988..1023131 26863196 MeRIP-seq:(Medium) rs900067632 Functional Loss SNV dbSNP153 33..33 33 - - - 103779 RMVar_ID_103779 Human_SNP_ID_614567245 m1A Human chr17 - 1031615 1031615 1031615 CCGGCGCCCGGCTCTGGGGCCGCGTGCGCAACAAGCTGCTCCGAAACAAGGTGCCCGCGGGGGCT CCGGCGCCCGGCTCTGGGGCCGCGTGCGCAACCAGCTGCTCCGAAACAAGGTGCCCGCGGGGGCT T G ABR Ensembl:ENSG00000159842 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1031610..1031791 26863196 MeRIP-seq:(Medium) rs985570211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1756813,Human_Splice_Rec_1756913,Human_Splice_Rec_1757011,Human_Splice_Rec_1757025 RMVar_hsa_circ_91339,RMVar_hsa_circ_180950,RMVar_hsa_circ_180952,RMVar_hsa_circ_110228 103780 RMVar_ID_103780 Human_SNP_ID_614567289 m1A Human chr17 - 1031711 1031700 1031711 GCATGACCGACGTCCTGCCCCAGCCCGACTGCAGCCCGAAGGCGGGGCGCGAACCCCTGGCGCTG GCATGACCGACGTCCTGCCCCAGCCCGACTGC___________GGGGCGCGAACCCCTGGCGCTG CGCCTTCGGGCT C ABR Ensembl:ENSG00000159842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1031709..1031811 26863196 MeRIP-seq:(Medium) rs1567614070 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_3542376 RMVar_hsa_circ_91339,RMVar_hsa_circ_180950,RMVar_hsa_circ_180952,RMVar_hsa_circ_110228 103781 RMVar_ID_103781 Human_SNP_ID_614573304 m1A Human chr17 - 1050099 1050099 1050099 TGAGAAGTGCTATGACAAGACCAAGGTCAACAAGGACAACAATGAGATCGTGGACAAGATCATGG TGAGAAGTGCTATGACAAGACCAAGGTCAACAGGGACAACAATGAGATCGTGGACAAGATCATGG T C ABR Ensembl:ENSG00000159842 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1050008..1050116 26863196 MeRIP-seq:(Medium) rs776309356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1872251,Human_RBP_ID_18531024 Human_Splice_Rec_1756746,Human_Splice_Rec_1756747,Human_Splice_Rec_1756798,Human_Splice_Rec_1756799,Human_Splice_Rec_1756856,Human_Splice_Rec_1756857,Human_Splice_Rec_1756898,Human_Splice_Rec_1756899,Human_Splice_Rec_1756946,Human_Splice_Rec_1756947,Human_Splice_Rec_1757000,Human_Splice_Rec_1757001,Human_Splice_Rec_1757019,Human_Splice_Rec_1757032,Human_Splice_Rec_1757042 Human_miRNA_ID_2255435 RMVar_hsa_circ_50633,RMVar_hsa_circ_91339,RMVar_hsa_circ_180950,RMVar_hsa_circ_180952,RMVar_hsa_circ_110228,RMVar_hsa_circ_334699,RMVar_hsa_circ_336127,RMVar_hsa_circ_372052,RMVar_hsa_circ_299917,RMVar_hsa_circ_180955,RMVar_hsa_circ_180957,RMVar_hsa_circ_22687,RMVar_hsa_circ_180956,RMVar_hsa_circ_180954 103782 RMVar_ID_103782 Human_SNP_ID_614579168 m1A Human chr17 - 1067237 1067237 1067237 TCATGGCTCCCTCTGGCTCGTTTGCAGGAAGCACCAGCAGTATGACTGTAAGTGGTACATCCCCC TCATGGCTCCCTCTGGCTCGTTTGCAGGAAGCGCCAGCAGTATGACTGTAAGTGGTACATCCCCC T C ABR Ensembl:ENSG00000159842 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1067190..1067279 26863196 MeRIP-seq:(Medium) rs979875163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1756734,Human_Splice_Rec_1756786,Human_Splice_Rec_1756844,Human_Splice_Rec_1756886,Human_Splice_Rec_1756934,Human_Splice_Rec_1757052,Human_Splice_Rec_1757054,Human_Splice_Rec_1757074 RMVar_hsa_circ_50633,RMVar_hsa_circ_180952,RMVar_hsa_circ_110228,RMVar_hsa_circ_336127,RMVar_hsa_circ_299917,RMVar_hsa_circ_180957,RMVar_hsa_circ_22687,RMVar_hsa_circ_180956,RMVar_hsa_circ_32144,RMVar_hsa_circ_180960,RMVar_hsa_circ_180961,RMVar_hsa_circ_372474,RMVar_hsa_circ_180962,RMVar_hsa_circ_369282,RMVar_hsa_circ_180964,RMVar_hsa_circ_180965,RMVar_hsa_circ_180963 103783 RMVar_ID_103783 Human_SNP_ID_614589403 m1A Human chr17 - 1100731 1100731 1100731 CTGTTGGCTGTGCTTTGCGTTTGTGCAGGTGGAAGCAGGGAAAGGCCTGGAGATGAGGAAGCTGG CTGTTGGCTGTGCTTTGCGTTTGTGCAGGTGGCAGCAGGGAAAGGCCTGGAGATGAGGAAGCTGG T G ABR Ensembl:ENSG00000159842 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:1100714..1100788;chr17:1100713..1109012 26863196,32194978 MeRIP-seq:(Medium) rs962601920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1756720,Human_Splice_Rec_1756721,Human_Splice_Rec_1756772,Human_Splice_Rec_1756773,Human_Splice_Rec_1756830,Human_Splice_Rec_1756831,Human_Splice_Rec_1756872,Human_Splice_Rec_1756873,Human_Splice_Rec_1757084,Human_Splice_Rec_1757085,Human_Splice_Rec_1757106,Human_Splice_Rec_1757107,Human_Splice_Rec_1757112,Human_Splice_Rec_1757113,Human_Splice_Rec_1757120,Human_Splice_Rec_1757121 RMVar_hsa_circ_299917,RMVar_hsa_circ_180957,RMVar_hsa_circ_22687,RMVar_hsa_circ_372474,RMVar_hsa_circ_305883,RMVar_hsa_circ_180963,RMVar_hsa_circ_180966,RMVar_hsa_circ_327226,RMVar_hsa_circ_18865,RMVar_hsa_circ_180969,RMVar_hsa_circ_180970,RMVar_hsa_circ_41752,RMVar_hsa_circ_362855,RMVar_hsa_circ_291936,RMVar_hsa_circ_180972,RMVar_hsa_circ_301465,RMVar_hsa_circ_68084,RMVar_hsa_circ_77836,RMVar_hsa_circ_180973,RMVar_hsa_circ_180974 103784 RMVar_ID_103784 Human_SNP_ID_614591673 m1A Human chr17 - 1107753 1107753 1107753 CCACCCTGTCTTCTCTGATCTGGTGCTGGCGTAGGGCCGTGGGGGTAAGTCACGTCTCCCCGTGG CCACCCTGTCTTCTCTGATCTGGTGCTGGCGTGGGGCCGTGGGGGTAAGTCACGTCTCCCCGTGG T C ABR Ensembl:ENSG00000159842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1107746..1107944 26863196 MeRIP-seq:(Medium) rs879297739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22687,RMVar_hsa_circ_18865,RMVar_hsa_circ_68084 103785 RMVar_ID_103785 Human_SNP_ID_614592123 m1A Human chr17 - 1109045 1109045 1109045 CCGGCTGCCATGGAGGAGGAAGAGGAGGCGATAGGCTTGCTGGACAAGGTTCTGGAGGACGAAGA CCGGCTGCCATGGAGGAGGAAGAGGAGGCGATCGGCTTGCTGGACAAGGTTCTGGAGGACGAAGA T G ABR Ensembl:ENSG00000159842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:1108957..1109060;chr17:1108902..1109069 26863196 MeRIP-seq:(Medium) rs1159099564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22687,RMVar_hsa_circ_18865,RMVar_hsa_circ_68084 103786 RMVar_ID_103786 Human_SNP_ID_614607762 m1A Human chr17 + 1159545 1159541 1159546 GGAGAAGTAGGAATGCGGTACTCACACACGGGAGAAGTAGGAATGCGGTACTCACACACGGGAGA GGAGAAGTAGGAATGCGGTACTCACACAC_____AAGTAGGAATGCGGTACTCACACACGGGAGA CGGGAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:1159519..1159674;chr17:1159542..1159654 26863196,32194978 MeRIP-seq:(Medium) rs1567841372 Functional Loss DEL dbSNP153 30..34 33 - - - 103787 RMVar_ID_103787 Human_SNP_ID_614607769 m1A Human chr17 + 1159545 1159543 1159545 GGAGAAGTAGGAATGCGGTACTCACACACGGGAGAAGTAGGAATGCGGTACTCACACACGGGAGA GGAGAAGTAGGAATGCGGTACTCACACACGG__GAAGTAGGAATGCGGTACTCACACACGGGAGA GGA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:1159519..1159674;chr17:1159542..1159654 26863196,32194978 MeRIP-seq:(Medium) rs1567841387 Functional Loss DEL dbSNP153 32..33 33 - - - 103788 RMVar_ID_103788 Human_SNP_ID_614607771 m1A Human chr17 + 1159545 1159545 1159545 GGAGAAGTAGGAATGCGGTACTCACACACGGGAGAAGTAGGAATGCGGTACTCACACACGGGAGA GGAGAAGTAGGAATGCGGTACTCACACACGGGGGAAGTAGGAATGCGGTACTCACACACGGGAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:1159519..1159674;chr17:1159542..1159654 26863196,32194978 MeRIP-seq:(Medium) rs1469323348 Functional Loss SNV dbSNP153 33..33 33 - - - 103789 RMVar_ID_103789 Human_SNP_ID_614614156 m1A Human chr17 + 1179862 1179862 1179862 GGGGCGAGGAGGCCGGGAACCAGGTCCCCGGGAGGAGCGCGGGGCGGCCGGGGCAGGGGCGAGGG GGGGCGAGGAGGCCGGGAACCAGGTCCCCGGGGGGAGCGCGGGGCGGCCGGGGCAGGGGCGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1179826..1179929 26863196 MeRIP-seq:(Medium) rs1166349413 Functional Loss SNV dbSNP153 33..33 33 - - - 103790 RMVar_ID_103790 Human_SNP_ID_614668050 m1A Human chr17 + 1344672 1344670 1344672 AGATATCCAGTAGTACAAATTAGCTTCAAGTTACACATACTGAACAAAAGAGGTTGAGCGAGCGA AGATATCCAGTAGTACAAATTAGCTTCAAGT__CACATACTGAACAAAAGAGGTTGAGCGAGCGA TTA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1344621..1344722 32194978 MeRIP-seq:(Medium) rs1374981327 Functional Loss DEL dbSNP153 32..33 33 - - - 103791 RMVar_ID_103791 Human_SNP_ID_614668080 m1A Human chr17 + 1344758 1344757 1344758 AGGAGGTAGGGGGAGGGGGAAGGAGAAGAAACAAAAGAATTGAACAGGCATGCAGGCTTTTCCAT AGGAGGTAGGGGGAGGGGGAAGGAGAAGAAAC_AAAGAATTGAACAGGCATGCAGGCTTTTCCAT CA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1344716..1344805 26863196 MeRIP-seq:(Medium) rs747741427 Functional Loss DEL dbSNP153 33..33 33 - - - 103792 RMVar_ID_103792 Human_SNP_ID_614674423 m1A Human chr17 - 1361249 1361249 1361249 GGTATCTGGCAGAATTTGCCACAGGAAACGACAGGAAGGAGGCTGCGGAGAACAGCCTAGTGGCT GGTATCTGGCAGAATTTGCCACAGGAAACGACCGGAAGGAGGCTGCGGAGAACAGCCTAGTGGCT T G YWHAE Ensembl:ENSG00000108953 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs754788015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47616,Human_RBP_ID_482996,Human_RBP_ID_1527807,Human_RBP_ID_1848657,Human_RBP_ID_2493387,Human_RBP_ID_4405608,Human_RBP_ID_6558702,Human_RBP_ID_9069041,Human_RBP_ID_12886317,Human_RBP_ID_18688956,Human_RBP_ID_22498704,Human_RBP_ID_23710919,Human_RBP_ID_26954018 Human_Splice_Rec_1757150,Human_Splice_Rec_1757166 RMVar_hsa_circ_30847,RMVar_hsa_circ_273626,RMVar_hsa_circ_93985,RMVar_hsa_circ_338270,RMVar_hsa_circ_180978,RMVar_hsa_circ_292129,RMVar_hsa_circ_180979,RMVar_hsa_circ_180980,RMVar_hsa_circ_270425,RMVar_hsa_circ_277999,RMVar_hsa_circ_96697,RMVar_hsa_circ_180981,RMVar_hsa_circ_180982,RMVar_hsa_circ_180983 103793 RMVar_ID_103793 Human_SNP_ID_614674934 m1A Human chr17 - 1362917 1362917 1362917 CATCAGCTTGTGAGGAGGAAGAGTTTGGAGTAATAGAGCAGTCATTGAGTATGCAAGGAGCTAGG CATCAGCTTGTGAGGAGGAAGAGTTTGGAGTATTAGAGCAGTCATTGAGTATGCAAGGAGCTAGG T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1362915..1363023 26863196 MeRIP-seq:(Medium) rs1019974213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558745,Human_RBP_ID_9844734,Human_RBP_ID_12886379,Human_RBP_ID_23710942,Human_RBP_ID_27661622 RMVar_hsa_circ_93985,RMVar_hsa_circ_338270,RMVar_hsa_circ_180978,RMVar_hsa_circ_292129,RMVar_hsa_circ_180979,RMVar_hsa_circ_270425,RMVar_hsa_circ_96697,RMVar_hsa_circ_180982,RMVar_hsa_circ_180983 103794 RMVar_ID_103794 Human_SNP_ID_614680979 m1A Human chr17 + 1380791 1380791 1380791 TTTCCATTCTTACATCTCATATATTTAATCCCATATCTGTGCTTTTGGTAACATATCCAAAGAAC TTTCCATTCTTACATCTCATATATTTAATCCCCTATCTGTGCTTTTGGTAACATATCCAAAGAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1380787..1380912 26863196 MeRIP-seq:(Medium) rs1011279193 Functional Loss SNV dbSNP153 33..33 33 - - - 103795 RMVar_ID_103795 Human_SNP_ID_614680980 m1A Human chr17 + 1380791 1380791 1380791 TTTCCATTCTTACATCTCATATATTTAATCCCATATCTGTGCTTTTGGTAACATATCCAAAGAAC TTTCCATTCTTACATCTCATATATTTAATCCCGTATCTGTGCTTTTGGTAACATATCCAAAGAAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1380787..1380912 26863196 MeRIP-seq:(Medium) rs1011279193 Functional Loss SNV dbSNP153 33..33 33 - - - 103796 RMVar_ID_103796 Human_SNP_ID_614688112 m1A Human chr17 - 1400030 1400030 1400030 GCTGAGCGATACGACGGTGAGTTGGGGGGGCAACGGGGGGCTGGAATTCTCGGACCCTCTGCCGC GCTGAGCGATACGACGGTGAGTTGGGGGGGCATCGGGGGGCTGGAATTCTCGGACCCTCTGCCGC T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:1400026..1400075 26863196 MeRIP-seq:(Medium) rs369088116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6158,Human_RBP_ID_47625,Human_RBP_ID_5361436,Human_RBP_ID_24552220 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103797 RMVar_ID_103797 Human_SNP_ID_614688113 m1A Human chr17 - 1400030 1400030 1400030 GCTGAGCGATACGACGGTGAGTTGGGGGGGCAACGGGGGGCTGGAATTCTCGGACCCTCTGCCGC GCTGAGCGATACGACGGTGAGTTGGGGGGGCAGCGGGGGGCTGGAATTCTCGGACCCTCTGCCGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:1400026..1400075 26863196 MeRIP-seq:(Medium) rs369088116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6158,Human_RBP_ID_47625,Human_RBP_ID_5361436,Human_RBP_ID_24552220 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103798 RMVar_ID_103798 Human_SNP_ID_614688114 m1A Human chr17 - 1400030 1400030 1400030 GCTGAGCGATACGACGGTGAGTTGGGGGGGCAACGGGGGGCTGGAATTCTCGGACCCTCTGCCGC GCTGAGCGATACGACGGTGAGTTGGGGGGGCACCGGGGGGCTGGAATTCTCGGACCCTCTGCCGC T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:1400026..1400075 26863196 MeRIP-seq:(Medium) rs369088116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6158,Human_RBP_ID_47625,Human_RBP_ID_5361436,Human_RBP_ID_24552220 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103799 RMVar_ID_103799 Human_SNP_ID_614688178 m1A Human chr17 + 1400145 1400145 1400145 CGGCAGCGGCTCCGGCAGGGTCTGCGCGACGGATGGAAGCGGATAGTGTCTCCGACTCTCTCAGC CGGCAGCGGCTCCGGCAGGGTCTGCGCGACGGTTGGAAGCGGATAGTGTCTCCGACTCTCTCAGC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1399996..1400225 26863410 MeRIP-seq:(Medium) rs1033374726 Functional Loss SNV dbSNP153 33..33 33 - - - 103800 RMVar_ID_103800 Human_SNP_ID_614688190 m1A Human chr17 - 1400156 1400156 1400156 CGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACCCTGCCGG CGGAGCGAGAGGCTGAGAGAGTCGGAGACACTGTCCGCTTCCATCCGTCGCGCAGACCCTGCCGG T C YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1399797..1400225 26863196 MeRIP-seq:(Medium) rs747128604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_483047,Human_RBP_ID_1006167,Human_RBP_ID_1180097,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419796,Human_RBP_ID_5441097,Human_RBP_ID_5466077,Human_RBP_ID_5496481,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813032,Human_RBP_ID_9069081,Human_RBP_ID_9286615,Human_RBP_ID_9326403,Human_RBP_ID_9375013,Human_RBP_ID_12888879,Human_RBP_ID_17257873,Human_RBP_ID_17373902,Human_RBP_ID_17488936,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_20175390,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103801 RMVar_ID_103801 Human_SNP_ID_614688191 m1A Human chr17 - 1400156 1400156 1400156 CGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACCCTGCCGG CGGAGCGAGAGGCTGAGAGAGTCGGAGACACTCTCCGCTTCCATCCGTCGCGCAGACCCTGCCGG T G YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1399797..1400225 26863196 MeRIP-seq:(Medium) rs747128604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_483047,Human_RBP_ID_1006167,Human_RBP_ID_1180097,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419796,Human_RBP_ID_5441097,Human_RBP_ID_5466077,Human_RBP_ID_5496481,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813032,Human_RBP_ID_9069081,Human_RBP_ID_9286615,Human_RBP_ID_9326403,Human_RBP_ID_9375013,Human_RBP_ID_12888879,Human_RBP_ID_17257873,Human_RBP_ID_17373902,Human_RBP_ID_17488936,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_20175390,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103802 RMVar_ID_103802 Human_SNP_ID_614688194 m1A Human chr17 - 1400159 1400159 1400159 ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACCCTGC ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACTCTATCCGCTTCCATCCGTCGCGCAGACCCTGC T A YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1400151..1400175 26863196 MeRIP-seq:(Medium) rs777019698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_483047,Human_RBP_ID_764946,Human_RBP_ID_1006167,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419796,Human_RBP_ID_5441097,Human_RBP_ID_5466077,Human_RBP_ID_5496481,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9069081,Human_RBP_ID_9286615,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17257873,Human_RBP_ID_17373902,Human_RBP_ID_17488936,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26447191,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103803 RMVar_ID_103803 Human_SNP_ID_614688195 m1A Human chr17 - 1400159 1400159 1400159 ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACCCTGC ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACGCTATCCGCTTCCATCCGTCGCGCAGACCCTGC T C YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1400151..1400175 26863196 MeRIP-seq:(Medium) rs777019698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_483047,Human_RBP_ID_764946,Human_RBP_ID_1006167,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419796,Human_RBP_ID_5441097,Human_RBP_ID_5466077,Human_RBP_ID_5496481,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9069081,Human_RBP_ID_9286615,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17257873,Human_RBP_ID_17373902,Human_RBP_ID_17488936,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26447191,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103804 RMVar_ID_103804 Human_SNP_ID_614688196 m1A Human chr17 - 1400159 1400159 1400159 ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACCCTGC ACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACCCTATCCGCTTCCATCCGTCGCGCAGACCCTGC T G YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1400151..1400175 26863196 MeRIP-seq:(Medium) rs777019698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_483047,Human_RBP_ID_764946,Human_RBP_ID_1006167,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419796,Human_RBP_ID_5441097,Human_RBP_ID_5466077,Human_RBP_ID_5496481,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9069081,Human_RBP_ID_9286615,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17257873,Human_RBP_ID_17373902,Human_RBP_ID_17488936,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26447191,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103805 RMVar_ID_103805 Human_SNP_ID_614688202 m1A Human chr17 - 1400163 1400163 1400163 CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACC CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGGGACACTATCCGCTTCCATCCGTCGCGCAGACC T C YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:1399994..1400225;chr17:1399804..1400225;chr17:1399907..1400225 26863196 MeRIP-seq:(Medium) rs868169662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_764946,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419797,Human_RBP_ID_5466077,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103806 RMVar_ID_103806 Human_SNP_ID_614688203 m1A Human chr17 - 1400163 1400163 1400163 CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACC CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGCGACACTATCCGCTTCCATCCGTCGCGCAGACC T G YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:1399994..1400225;chr17:1399804..1400225;chr17:1399907..1400225 26863196 MeRIP-seq:(Medium) rs868169662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47626,Human_RBP_ID_764946,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419797,Human_RBP_ID_5466077,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 103807 RMVar_ID_103807 Human_SNP_ID_614695865 m1A Human chr17 - 1422168 1422168 1422168 CAGGGCAAGACTCAGTCTCAAAAAAAAAAAAAAGGAAAAAAAAAAGAAAAAAAAATGTTGAACCA CAGGGCAAGACTCAGTCTCAAAAAAAAAAAAAGGGAAAAAAAAAAGAAAAAAAAATGTTGAACCA T C CRK Ensembl:ENSG00000167193 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1341851350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25249375 Human_miRNA_ID_1715236 RMVar_hsa_circ_180986,RMVar_hsa_circ_76030 103808 RMVar_ID_103808 Human_SNP_ID_614701068 m1A Human chr17 - 1436925 1436925 1436925 ATGAGGAAGATCTTCCCTTTAAGAAAGGAGACATCTTGAGAATCCGGGACAAGCCTGAAGAGCAG ATGAGGAAGATCTTCCCTTTAAGAAAGGAGACGTCTTGAGAATCCGGGACAAGCCTGAAGAGCAG T C CRK Ensembl:ENSG00000167193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1436875..1437090 26863196 MeRIP-seq:(Medium) rs745921349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1527942,Human_RBP_ID_1848896,Human_RBP_ID_3512312,Human_RBP_ID_6559639,Human_RBP_ID_8813091,Human_RBP_ID_12889514,Human_RBP_ID_18530436,Human_RBP_ID_18987501,Human_RBP_ID_23711297,Human_RBP_ID_26330621 Human_miRNA_ID_2781649,Human_miRNA_ID_2781650,Human_miRNA_ID_2787213,Human_miRNA_ID_2787214 RMVar_hsa_circ_180987,RMVar_hsa_circ_278968,RMVar_hsa_circ_180988,RMVar_hsa_circ_282254 103809 RMVar_ID_103809 Human_SNP_ID_614701090 m1A Human chr17 + 1437014 1437014 1437014 CTCGCACATACTCCGCCTCCTCCTGCCTGAGAATCACTCCACTACCCTGCCTGGATCTGGAAACT CTCGCACATACTCCGCCTCCTCCTGCCTGAGAGTCACTCCACTACCCTGCCTGGATCTGGAAACT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1436876..1437134 26863196 MeRIP-seq:(Medium) rs776671383 Functional Loss SNV dbSNP153 33..33 33 - - - 103810 RMVar_ID_103810 Human_SNP_ID_614707474 m1A Human chr17 - 1455925 1455925 1455925 ACTCGCGCGTCTCCCACTACATCATCAACAGCAGCGGCCCGCGCCCGCCGGTGCCACCGTCGCCC ACTCGCGCGTCTCCCACTACATCATCAACAGCGGCGGCCCGCGCCCGCCGGTGCCACCGTCGCCC T C CRK Ensembl:ENSG00000167193 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:1455918..1456069 26863410 MeRIP-seq:(Medium) rs1291990121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9327108,Human_RBP_ID_17885324,Human_RBP_ID_27448428 Human_Splice_Rec_1757205,Human_Splice_Rec_1757209,Human_Splice_Rec_1757213 103811 RMVar_ID_103811 Human_SNP_ID_614707537 m1A Human chr17 - 1456107 1456107 1456107 GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCAACTTCGACTCGGAGGAGCGGAGTAGCTGGTACT GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCATCTTCGACTCGGAGGAGCGGAGTAGCTGGTACT T A CRK Ensembl:ENSG00000167193 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:1456018..1456225 26863196 MeRIP-seq:(Medium) rs774008957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464203,Human_RBP_ID_5420695,Human_RBP_ID_5466081,Human_RBP_ID_6560096,Human_RBP_ID_8191633,Human_RBP_ID_9353360,Human_RBP_ID_12891367,Human_RBP_ID_18419816 103812 RMVar_ID_103812 Human_SNP_ID_614707538 m1A Human chr17 - 1456107 1456107 1456107 GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCAACTTCGACTCGGAGGAGCGGAGTAGCTGGTACT GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCAGCTTCGACTCGGAGGAGCGGAGTAGCTGGTACT T C CRK Ensembl:ENSG00000167193 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:1456018..1456225 26863196 MeRIP-seq:(Medium) rs774008957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464203,Human_RBP_ID_5420695,Human_RBP_ID_5466081,Human_RBP_ID_6560096,Human_RBP_ID_8191633,Human_RBP_ID_9353360,Human_RBP_ID_12891367,Human_RBP_ID_18419816 103813 RMVar_ID_103813 Human_SNP_ID_614707539 m1A Human chr17 - 1456107 1456107 1456107 GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCAACTTCGACTCGGAGGAGCGGAGTAGCTGGTACT GCGTTTAGGCGCGGAGGCAGCCATGGCGGGCACCTTCGACTCGGAGGAGCGGAGTAGCTGGTACT T G CRK Ensembl:ENSG00000167193 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:1456018..1456225 26863196 MeRIP-seq:(Medium) rs774008957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464203,Human_RBP_ID_5420695,Human_RBP_ID_5466081,Human_RBP_ID_6560096,Human_RBP_ID_8191633,Human_RBP_ID_9353360,Human_RBP_ID_12891367,Human_RBP_ID_18419816 103814 RMVar_ID_103814 Human_SNP_ID_614710426 m1A Human chr17 - 1464990 1464990 1464990 CTGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCAC CTGACCTACATGGAGAAACTCCGCCTCTAGTAGAAATACAAAATTAGCCGGGCATGGTGGTGCAC T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1138604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108683,RMVar_hsa_circ_125640,RMVar_hsa_circ_127609,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_108952,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_92279,RMVar_hsa_circ_181000,RMVar_hsa_circ_84075,RMVar_hsa_circ_85313,RMVar_hsa_circ_181002,RMVar_hsa_circ_84069,RMVar_hsa_circ_181001,RMVar_hsa_circ_180998,RMVar_hsa_circ_180999,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989 103815 RMVar_ID_103815 Human_SNP_ID_614710428 m1A Human chr17 - 1464994 1464994 1464994 CAACCTGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGT CAACCTGACCTACATGGAGAAACTCCGCCTCTGGTAAAAATACAAAATTAGCCGGGCATGGTGGT T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1138603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25249956 Human_miRNA_ID_720476 RMVar_hsa_circ_108683,RMVar_hsa_circ_125640,RMVar_hsa_circ_127609,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_108952,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_92279,RMVar_hsa_circ_181000,RMVar_hsa_circ_84075,RMVar_hsa_circ_85313,RMVar_hsa_circ_181002,RMVar_hsa_circ_84069,RMVar_hsa_circ_181001,RMVar_hsa_circ_180998,RMVar_hsa_circ_180999,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989 103816 RMVar_ID_103816 Human_SNP_ID_614710491 m1A Human chr17 + 1465250 1465250 1465250 GACAGGTAAACAGACAGAAAGACAAGGTGCCAAGGGAATCAGGAGGAGAGGTGTCCTGGCCAGGG GACAGGTAAACAGACAGAAAGACAAGGTGCCAGGGGAATCAGGAGGAGAGGTGTCCTGGCCAGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:1465201..1465325 32194978 MeRIP-seq:(Medium) rs1567510085 Functional Loss SNV dbSNP153 33..33 33 - - - 103817 RMVar_ID_103817 Human_SNP_ID_614710638 m1A Human chr17 + 1465751 1465751 1465751 GCCTTTATCACCGAGAATTCAGCCGTGGGGCGACCTGTGGGGGCGGAGAGAGACGGCCAAGTGGT GCCTTTATCACCGAGAATTCAGCCGTGGGGCGCCCTGTGGGGGCGGAGAGAGACGGCCAAGTGGT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1465701..1465775 32194978 MeRIP-seq:(Medium) rs1260245427 Functional Loss SNV dbSNP153 33..33 33 - - - 103818 RMVar_ID_103818 Human_SNP_ID_614712592 m1A Human chr17 - 1470287 1470287 1470287 CGTCCTGCGCCACGCCCCCCGCTGCCCCGAGAACGCCTTCTTCCTGGACCATGTGCGCACCTCTT CGTCCTGCGCCACGCCCCCCGCTGCCCCGAGAGCGCCTTCTTCCTGGACCATGTGCGCACCTCTT T C MYO1C Ensembl:ENSG00000197879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1470173..1470439 26863196 MeRIP-seq:(Medium) rs530843682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132263,Human_RBP_ID_8813098 Human_Splice_Rec_1757268,Human_Splice_Rec_1757330,Human_Splice_Rec_1757392,Human_Splice_Rec_1757454,Human_Splice_Rec_1757518,Human_Splice_Rec_1757580,Human_Splice_Rec_1757642,Human_Splice_Rec_1757670,Human_Splice_Rec_1757678 RMVar_hsa_circ_31642,RMVar_hsa_circ_108683,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_108952,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180998,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_94354,RMVar_hsa_circ_84994,RMVar_hsa_circ_181006,RMVar_hsa_circ_181008,RMVar_hsa_circ_181007,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_123365,RMVar_hsa_circ_181013,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_127234,RMVar_hsa_circ_181015,RMVar_hsa_circ_181016,RMVar_hsa_circ_119656,RMVar_hsa_circ_181017 103819 RMVar_ID_103819 Human_SNP_ID_614712637 m1A Human chr17 - 1470336 1470336 1470336 CTCACCCCCAACCCTGTCTGGCCCCCCACCCCAGGCTCATCCGAGGCTTCGTCCTGCGCCACGCC CTCACCCCCAACCCTGTCTGGCCCCCCACCCCCGGCTCATCCGAGGCTTCGTCCTGCGCCACGCC T G MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1470333..1470418 26863196 MeRIP-seq:(Medium) rs1474965625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132263,Human_RBP_ID_22585010 RMVar_hsa_circ_31642,RMVar_hsa_circ_108683,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_94354,RMVar_hsa_circ_84994,RMVar_hsa_circ_181006,RMVar_hsa_circ_181008,RMVar_hsa_circ_181007,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_123365,RMVar_hsa_circ_181013,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_127234,RMVar_hsa_circ_181015,RMVar_hsa_circ_181016,RMVar_hsa_circ_119656,RMVar_hsa_circ_181017 103820 RMVar_ID_103820 Human_SNP_ID_614712739 m1A Human chr17 - 1470526 1470526 1470526 AAGAAGATAGAGTTCAGCCATCTGTGGTCTCCACGACAGCCATCTGCATCCAGTCGTGGTGGCGT AAGAAGATAGAGTTCAGCCATCTGTGGTCTCCCCGACAGCCATCTGCATCCAGTCGTGGTGGCGT T G MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1470524..1470608 26863196 MeRIP-seq:(Medium) rs1026541756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5363394 Human_Splice_Rec_1757267,Human_Splice_Rec_1757329,Human_Splice_Rec_1757391,Human_Splice_Rec_1757453,Human_Splice_Rec_1757517,Human_Splice_Rec_1757579,Human_Splice_Rec_1757641,Human_Splice_Rec_1757669,Human_Splice_Rec_1757677 RMVar_hsa_circ_31642,RMVar_hsa_circ_108683,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_94354,RMVar_hsa_circ_181006,RMVar_hsa_circ_181007,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_123365,RMVar_hsa_circ_181013,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_127234,RMVar_hsa_circ_181015,RMVar_hsa_circ_181016,RMVar_hsa_circ_119656,RMVar_hsa_circ_110486,RMVar_hsa_circ_181017,RMVar_hsa_circ_181018 103821 RMVar_ID_103821 Human_SNP_ID_614713028 m1A Human chr17 - 1471121 1471121 1471121 TCCCAGGACCAAGATCTTCATCCGCTTCCCCAAGACCCTGTTTGCCACAGAGGATGCCCTGGAGG TCCCAGGACCAAGATCTTCATCCGCTTCCCCAGGACCCTGTTTGCCACAGAGGATGCCCTGGAGG T C MYO1C Ensembl:ENSG00000197879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1471051..1471295 26863196 MeRIP-seq:(Medium) rs1357396132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444165,Human_RBP_ID_26330978 Human_Splice_Rec_1757262,Human_Splice_Rec_1757263,Human_Splice_Rec_1757324,Human_Splice_Rec_1757325,Human_Splice_Rec_1757386,Human_Splice_Rec_1757387,Human_Splice_Rec_1757448,Human_Splice_Rec_1757449,Human_Splice_Rec_1757512,Human_Splice_Rec_1757513,Human_Splice_Rec_1757574,Human_Splice_Rec_1757575,Human_Splice_Rec_1757636,Human_Splice_Rec_1757637,Human_Splice_Rec_1757673,Human_Splice_Rec_1757684,Human_Splice_Rec_1757685,Human_Splice_Rec_1757696 Human_miRNA_ID_2157946 RMVar_hsa_circ_31642,RMVar_hsa_circ_108683,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_94354,RMVar_hsa_circ_181006,RMVar_hsa_circ_181007,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_123365,RMVar_hsa_circ_181013,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_127234,RMVar_hsa_circ_181015,RMVar_hsa_circ_181016,RMVar_hsa_circ_119656,RMVar_hsa_circ_110486,RMVar_hsa_circ_181017,RMVar_hsa_circ_181018 103822 RMVar_ID_103822 Human_SNP_ID_614713029 m1A Human chr17 - 1471122 1471122 1471122 CTCCCAGGACCAAGATCTTCATCCGCTTCCCCAAGACCCTGTTTGCCACAGAGGATGCCCTGGAG CTCCCAGGACCAAGATCTTCATCCGCTTCCCCCAGACCCTGTTTGCCACAGAGGATGCCCTGGAG T G MYO1C Ensembl:ENSG00000197879 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:1470692..1471275 32194978 MeRIP-seq:(Medium) rs1259360619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444165,Human_RBP_ID_26330978 Human_Splice_Rec_1757262,Human_Splice_Rec_1757263,Human_Splice_Rec_1757324,Human_Splice_Rec_1757325,Human_Splice_Rec_1757386,Human_Splice_Rec_1757387,Human_Splice_Rec_1757448,Human_Splice_Rec_1757449,Human_Splice_Rec_1757512,Human_Splice_Rec_1757513,Human_Splice_Rec_1757574,Human_Splice_Rec_1757575,Human_Splice_Rec_1757636,Human_Splice_Rec_1757637,Human_Splice_Rec_1757673,Human_Splice_Rec_1757684,Human_Splice_Rec_1757685,Human_Splice_Rec_1757696 Human_miRNA_ID_2157946 RMVar_hsa_circ_31642,RMVar_hsa_circ_108683,RMVar_hsa_circ_127327,RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_180996,RMVar_hsa_circ_91614,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180997,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180995,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_94354,RMVar_hsa_circ_181006,RMVar_hsa_circ_181007,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_123365,RMVar_hsa_circ_181013,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_127234,RMVar_hsa_circ_181015,RMVar_hsa_circ_181016,RMVar_hsa_circ_119656,RMVar_hsa_circ_110486,RMVar_hsa_circ_181017,RMVar_hsa_circ_181018 103823 RMVar_ID_103823 Human_SNP_ID_614713937 m1A Human chr17 - 1473563 1473563 1473563 CCCAGAAGAGTGAGGTCAGTGAGTCCATAGGGAGGTGGAAGCCAGACTGCCTGGCAGGGAGGGCA CCCAGAAGAGTGAGGTCAGTGAGTCCATAGGGGGGTGGAAGCCAGACTGCCTGGCAGGGAGGGCA T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1473551..1473779 26863196 MeRIP-seq:(Medium) rs1291443685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_181006,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_181015,RMVar_hsa_circ_119656,RMVar_hsa_circ_76672,RMVar_hsa_circ_181017,RMVar_hsa_circ_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019 103824 RMVar_ID_103824 Human_SNP_ID_614713938 m1A Human chr17 - 1473569 1473569 1473569 GGGAGCCCCAGAAGAGTGAGGTCAGTGAGTCCATAGGGAGGTGGAAGCCAGACTGCCTGGCAGGG GGGAGCCCCAGAAGAGTGAGGTCAGTGAGTCCGTAGGGAGGTGGAAGCCAGACTGCCTGGCAGGG T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1473567..1473764 26863196 MeRIP-seq:(Medium) rs1040439231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_181006,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_181015,RMVar_hsa_circ_119656,RMVar_hsa_circ_76672,RMVar_hsa_circ_181017,RMVar_hsa_circ_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019 103825 RMVar_ID_103825 Human_SNP_ID_614714390 m1A Human chr17 - 1474805 1474805 1474805 ACCTTCTCTTCCGGAACCTTAAGGAGGTGAGGAGGACGTGGGGAGGCCGGGGTGGGGGTGGGGAT ACCTTCTCTTCCGGAACCTTAAGGAGGTGAGGGGGACGTGGGGAGGCCGGGGTGGGGGTGGGGAT T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:1474801..1474850 32194978 MeRIP-seq:(Medium) rs1163344841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1757252,Human_Splice_Rec_1757314,Human_Splice_Rec_1757376,Human_Splice_Rec_1757438,Human_Splice_Rec_1757502,Human_Splice_Rec_1757564,Human_Splice_Rec_1757626 RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84075,RMVar_hsa_circ_84069,RMVar_hsa_circ_180992,RMVar_hsa_circ_180994,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_370014,RMVar_hsa_circ_98257,RMVar_hsa_circ_181003,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_181006,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_60790,RMVar_hsa_circ_121839,RMVar_hsa_circ_181015,RMVar_hsa_circ_119656,RMVar_hsa_circ_76672,RMVar_hsa_circ_181017,RMVar_hsa_circ_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_337863 103826 RMVar_ID_103826 Human_SNP_ID_614715423 m1A Human chr17 - 1477973 1477973 1477973 CACGGTGATCCCTTCCTTCCCTTCTGCCCCTCAGTGGGAGCCCGTCCAGTATTTCAACAACAAAA CACGGTGATCCCTTCCTTCCCTTCTGCCCCTCGGTGGGAGCCCGTCCAGTATTTCAACAACAAAA T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:1477926..1477975 32194978 MeRIP-seq:(Medium) rs756986598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1757247,Human_Splice_Rec_1757309,Human_Splice_Rec_1757371,Human_Splice_Rec_1757433,Human_Splice_Rec_1757497,Human_Splice_Rec_1757559,Human_Splice_Rec_1757621,Human_Splice_Rec_1757699 RMVar_hsa_circ_118026,RMVar_hsa_circ_124228,RMVar_hsa_circ_101078,RMVar_hsa_circ_108521,RMVar_hsa_circ_84069,RMVar_hsa_circ_180992,RMVar_hsa_circ_180993,RMVar_hsa_circ_180990,RMVar_hsa_circ_180991,RMVar_hsa_circ_180989,RMVar_hsa_circ_98257,RMVar_hsa_circ_114156,RMVar_hsa_circ_88755,RMVar_hsa_circ_181006,RMVar_hsa_circ_181004,RMVar_hsa_circ_181005,RMVar_hsa_circ_121839,RMVar_hsa_circ_181015,RMVar_hsa_circ_119656,RMVar_hsa_circ_76672,RMVar_hsa_circ_181017,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_9538,RMVar_hsa_circ_68952,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_181022,RMVar_hsa_circ_93895,RMVar_hsa_circ_372216,RMVar_hsa_circ_67920,RMVar_hsa_circ_40115,RMVar_hsa_circ_181023,RMVar_hsa_circ_53990 103827 RMVar_ID_103827 Human_SNP_ID_614718125 m1A Human chr17 + 1484209 1484209 1484209 GCAGGTTCTCGATGAAGGCGGCCTCGCTGGTGAAGTTCTCCAGCAGCACGAAATCCTGCACCCCC GCAGGTTCTCGATGAAGGCGGCCTCGCTGGTGCAGTTCTCCAGCAGCACGAAATCCTGCACCCCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1484159..1484325 26863196 MeRIP-seq:(Medium) rs765357187 Functional Loss SNV dbSNP153 33..33 33 - - - 103828 RMVar_ID_103828 Human_SNP_ID_614718126 m1A Human chr17 + 1484209 1484209 1484209 GCAGGTTCTCGATGAAGGCGGCCTCGCTGGTGAAGTTCTCCAGCAGCACGAAATCCTGCACCCCC GCAGGTTCTCGATGAAGGCGGCCTCGCTGGTGGAGTTCTCCAGCAGCACGAAATCCTGCACCCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1484159..1484325 26863196 MeRIP-seq:(Medium) rs765357187 Functional Loss SNV dbSNP153 33..33 33 - - - 103829 RMVar_ID_103829 Human_SNP_ID_614720292 m1A Human chr17 + 1490544 1490544 1490544 CAACAACAAAAACAAACAAAAACCTCACCTCCATCACTGCTCCTTACCTGGGCCAAGACAGCAGC CAACAACAAAAACAAACAAAAACCTCACCTCCGTCACTGCTCCTTACCTGGGCCAAGACAGCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1490540..1491203 26863196 MeRIP-seq:(Medium) rs1019626456 Functional Loss SNV dbSNP153 33..33 33 - - - 103830 RMVar_ID_103830 Human_SNP_ID_614720638 m1A Human chr17 + 1491462 1491462 1491462 CGCCTCCGGGTCGTGGGACCCCCCCCCCCCGCACGGGTCCACGCGGCCGTTCTTCGGCCCCAGCG CGCCTCCGGGTCGTGGGACCCCCCCCCCCCGCCCGGGTCCACGCGGCCGTTCTTCGGCCCCAGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1491458..1491675 26863196 MeRIP-seq:(Medium) rs1212680395 Functional Loss SNV dbSNP153 33..33 33 - - - 103831 RMVar_ID_103831 Human_SNP_ID_614720675 m1A Human chr17 + 1491557 1491557 1491557 GGCGGCTCCCGGCCCGGCCGCCCGCTCCCCACACCCGCCCCCCGCGGCCGCCGTCCCCGCGCCCC GGCGGCTCCCGGCCCGGCCGCCCGCTCCCCACCCCCGCCCCCCGCGGCCGCCGTCCCCGCGCCCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1491556..1491675 26863410 MeRIP-seq:(Medium) rs990912407 Functional Loss SNV dbSNP153 33..33 33 - - - 103832 RMVar_ID_103832 Human_SNP_ID_614725714 m1A Human chr17 + 1508166 1508166 1508166 CCACCGTAGCACCGATTTTTAATGGATTCCCGAACAAAGTGCAACCCAAAGTCCTCGATCCGAAA CCACCGTAGCACCGATTTTTAATGGATTCCCGGACAAAGTGCAACCCAAAGTCCTCGATCCGAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1507693..1508253 32194978 MeRIP-seq:(Medium) rs977699234 Functional Loss SNV dbSNP153 33..33 33 - - - 103833 RMVar_ID_103833 Human_SNP_ID_614728520 m1A Human chr17 + 1517726 1517726 1517726 ATAAATGTTTTGCTTGTTTGGTAGGGTGGATAAAGAGGAAGATGTGAAGAGGAGGCAGACAAAAG ATAAATGTTTTGCTTGTTTGGTAGGGTGGATAGAGAGGAAGATGTGAAGAGGAGGCAGACAAAAG A G PITPNA-AS1 Ensembl:ENSG00000236618 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1516979..1517867 32194978 MeRIP-seq:(Medium) rs142230526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901455,Human_RBP_ID_1546784,Human_RBP_ID_3512694,Human_RBP_ID_4468007,Human_RBP_ID_5188431,Human_RBP_ID_5581922,Human_RBP_ID_8255094 Human_Splice_Rec_1757932 103834 RMVar_ID_103834 Human_SNP_ID_614728707 m1A Human chr17 - 1518413 1518413 1518413 CTTCTTTTAAGTACCCCCTTTCCTCCTCACCCACCTCCAAACTGACTAGCACTCAGAGGGACTTA CTTCTTTTAAGTACCCCCTTTCCTCCTCACCCTCCTCCAAACTGACTAGCACTCAGAGGGACTTA T A PITPNA Ensembl:ENSG00000174238 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1518365..1518615 32194978 MeRIP-seq:(Medium) rs1567571922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8192655,Human_RBP_ID_17373980,Human_RBP_ID_17885482,Human_RBP_ID_26456966,Human_RBP_ID_27460072 103835 RMVar_ID_103835 Human_SNP_ID_614741371 m1A Human chr17 - 1562721 1562721 1562721 AGCGGCGCGAGAGGCGACGAGGCCCGGGCGGCAGGAGCCGGCGCGGCGACCGCGGCGAGGGCGGC AGCGGCGCGAGAGGCGACGAGGCCCGGGCGGCCGGAGCCGGCGCGGCGACCGCGGCGAGGGCGGC T G PITPNA Ensembl:ENSG00000174238 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:1561290..1562825;chr17:1562360..1562825 26863196 MeRIP-seq:(Medium) rs1243434293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4406553,Human_RBP_ID_22959325 103836 RMVar_ID_103836 Human_SNP_ID_614745181 m1A Human chr17 + 1574863 1574863 1574863 GTCCACCTCCACAAAAGCAGCTGTGTGTATGTACGGGGTGCCCTGGCGGCGGTCCTCAAATTCCC GTCCACCTCCACAAAAGCAGCTGTGTGTATGTCCGGGGTGCCCTGGCGGCGGTCCTCAAATTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1574815..1574922 26863196 MeRIP-seq:(Medium) rs1305207255 Functional Loss SNV dbSNP153 33..33 33 - - - 103837 RMVar_ID_103837 Human_SNP_ID_614758773 m1A Human chr17 + 1616756 1616756 1616756 TGCCCCGGCTCTGCTGTGCCGCCCACTGTGCCATTGGTGACATTCTCTGTGTGAAGAGGGAAGGA TGCCCCGGCTCTGCTGTGCCGCCCACTGTGCCGTTGGTGACATTCTCTGTGTGAAGAGGGAAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1616707..1616813 26863196 MeRIP-seq:(Medium) rs1469767384 Functional Loss SNV dbSNP153 33..33 33 - - - 103838 RMVar_ID_103838 Human_SNP_ID_614760679 m1A Human chr17 - 1623673 1623673 1623673 CCTGGAGGAGAGGAGGATACGCCCTGGAGGAGAGGAGGGTACGCCCTGGAGGAGAGGAGGGTACA CCTGGAGGAGAGGAGGATACGCCCTGGAGGAGGGGAGGGTACGCCCTGGAGGAGAGGAGGGTACA T C SLC43A2 Ensembl:ENSG00000167703 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1623597..1623737 26863196 MeRIP-seq:(Medium) rs1268911153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181065 103839 RMVar_ID_103839 Human_SNP_ID_614769284 m1A Human chr17 + 1649471 1649470 1649471 GGAGGCGCTCGTTCTCCTCCCGCAGCCGCCGCAGCTCCTGCTCCGCCGGCTGCGCCGACACCTGC GGAGGCGCTCGTTCTCCTCCCGCAGCCGCCGC_GCTCCTGCTCCGCCGGCTGCGCCGACACCTGC CA C NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1649420..1649488 26863196 MeRIP-seq:(Medium) rs1205709110 Functional Loss DEL dbSNP153 33..33 33 - - - 103840 RMVar_ID_103840 Human_SNP_ID_614769399 m1A Human chr17 - 1649659 1649659 1649659 GCTGCAGGATCTGGCGCGCCGTTTCGGGCCGGAGGCGGCGGCCGGGCTGGTGCCGCTAGTGGTGC GCTGCAGGATCTGGCGCGCCGTTTCGGGCCGGTGGCGGCGGCCGGGCTGGTGCCGCTAGTGGTGC T A RILP Ensembl:ENSG00000167705 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1649621..1649758 26863196 MeRIP-seq:(Medium) rs1163475198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5237562,Human_RBP_ID_17126539 Human_Splice_Rec_1758369 103841 RMVar_ID_103841 Human_SNP_ID_614769897 m1A Human chr17 + 1650782 1650782 1650782 GAGGGGCTGAGGCTTCGGCCTCGGGAGGCTGAAGCAGGAGGCAGGGAAACGGTCAGGCATACAGG GAGGGGCTGAGGCTTCGGCCTCGGGAGGCTGACGCAGGAGGCAGGGAAACGGTCAGGCATACAGG A C NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1650735..1650816 26863196 MeRIP-seq:(Medium) rs755301689 Functional Loss SNV dbSNP153 33..33 33 - - - 103842 RMVar_ID_103842 Human_SNP_ID_614769954 m1A Human chr17 - 1650902 1650902 1650902 GAAATATGAGCTACAGCTGGCGAACCCCAAAGAGTTCTACCACGAGGTGCACAGGCCCTCTCACT GAAATATGAGCTACAGCTGGCGAACCCCAAAGGGTTCTACCACGAGGTGCACAGGCCCTCTCACT T C PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs779481846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483412,Human_RBP_ID_1528053,Human_RBP_ID_1849217,Human_RBP_ID_3512903,Human_RBP_ID_8813139,Human_RBP_ID_9288564,Human_RBP_ID_17489056,Human_RBP_ID_17654455,Human_RBP_ID_18190675,Human_RBP_ID_26811759 Human_Splice_Rec_1758480,Human_Splice_Rec_1758562,Human_Splice_Rec_1758568 Human_miRNA_ID_2751077 RMVar_hsa_circ_89177,RMVar_hsa_circ_104681,RMVar_hsa_circ_123284,RMVar_hsa_circ_114758,RMVar_hsa_circ_94611,RMVar_hsa_circ_97701,RMVar_hsa_circ_93124,RMVar_hsa_circ_181073,RMVar_hsa_circ_181077,RMVar_hsa_circ_81151,RMVar_hsa_circ_87281,RMVar_hsa_circ_181079,RMVar_hsa_circ_77006,RMVar_hsa_circ_181080,RMVar_hsa_circ_181078,RMVar_hsa_circ_181075,RMVar_hsa_circ_181076,RMVar_hsa_circ_181074,RMVar_hsa_circ_181071,RMVar_hsa_circ_181072 103843 RMVar_ID_103843 Human_SNP_ID_614770088 m1A Human chr17 + 1651292 1651292 1651292 CCACTGGGGGTCAGCTTGTAGGCCGTCAGTGTACAGGAGCCTGGCGTGAAGCTGGGGGAGGAACG CCACTGGGGGTCAGCTTGTAGGCCGTCAGTGTGCAGGAGCCTGGCGTGAAGCTGGGGGAGGAACG A G NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1651101..1651325 32194978 MeRIP-seq:(Medium) rs753884759 Functional Loss SNV dbSNP153 33..33 33 - - - 103844 RMVar_ID_103844 Human_SNP_ID_614770171 m1A Human chr17 + 1651476 1651476 1651476 TCCCAAGATGGGTTGTCAGCCATGATCTTGGCATGGGTGGTGACATCCTGGGGTGATAACTGCGG TCCCAAGATGGGTTGTCAGCCATGATCTTGGCGTGGGTGGTGACATCCTGGGGTGATAACTGCGG A G NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1651451..1651475 26863196 MeRIP-seq:(Medium) rs1802491 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_644 GWAS_ID_13445,GWAS_ID_13446,GWAS_ID_13447,GWAS_ID_13448 103845 RMVar_ID_103845 Human_SNP_ID_614773363 m1A Human chr17 - 1662133 1662133 1662133 TACTACCTTTAGATTGTGAATAAGTGGAATACAGCTCTCATTGGCCTTATGACATACTTTCGGGA TACTACCTTTAGATTGTGAATAAGTGGAATACCGCTCTCATTGGCCTTATGACATACTTTCGGGA T G PRPF8 Ensembl:ENSG00000174231 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1661901..1662175 32194978 MeRIP-seq:(Medium) rs776123980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1006300,Human_RBP_ID_1528165,Human_RBP_ID_1849356,Human_RBP_ID_3513001,Human_RBP_ID_6561790,Human_RBP_ID_8813276,Human_RBP_ID_12897069,Human_RBP_ID_17258019,Human_RBP_ID_17489103,Human_RBP_ID_18289112,Human_RBP_ID_18689568,Human_RBP_ID_22055449,Human_RBP_ID_23712248,Human_RBP_ID_24532137 Human_Splice_Rec_1758444,Human_Splice_Rec_1758526 RMVar_hsa_circ_17614,RMVar_hsa_circ_89177,RMVar_hsa_circ_94611,RMVar_hsa_circ_97701,RMVar_hsa_circ_181077,RMVar_hsa_circ_87281,RMVar_hsa_circ_181079,RMVar_hsa_circ_181080,RMVar_hsa_circ_181078,RMVar_hsa_circ_103958,RMVar_hsa_circ_109990,RMVar_hsa_circ_181081,RMVar_hsa_circ_181082,RMVar_hsa_circ_123282,RMVar_hsa_circ_181083,RMVar_hsa_circ_127974,RMVar_hsa_circ_34902,RMVar_hsa_circ_104566,RMVar_hsa_circ_122485,RMVar_hsa_circ_181086,RMVar_hsa_circ_112343,RMVar_hsa_circ_79198,RMVar_hsa_circ_181088,RMVar_hsa_circ_181090,RMVar_hsa_circ_88992,RMVar_hsa_circ_181089,RMVar_hsa_circ_181087,RMVar_hsa_circ_77570,RMVar_hsa_circ_97043,RMVar_hsa_circ_181091,RMVar_hsa_circ_181092,RMVar_hsa_circ_181096,RMVar_hsa_circ_81865,RMVar_hsa_circ_124564,RMVar_hsa_circ_181098,RMVar_hsa_circ_77208,RMVar_hsa_circ_181097,RMVar_hsa_circ_116752,RMVar_hsa_circ_181102,RMVar_hsa_circ_105934,RMVar_hsa_circ_108793,RMVar_hsa_circ_181104,RMVar_hsa_circ_93529,RMVar_hsa_circ_181103,RMVar_hsa_circ_181100,RMVar_hsa_circ_181101,RMVar_hsa_circ_97823,RMVar_hsa_circ_181106 103846 RMVar_ID_103846 Human_SNP_ID_614775386 m1A Human chr17 - 1668216 1668214 1668216 GTTAGAGGCTGAGGAGTGGAGGAGTGTCTGAGAGGGTAAGGATGCAGTTGACTCTAGTGGTTAGA GTTAGAGGCTGAGGAGTGGAGGAGTGTCTGAG__GGTAAGGATGCAGTTGACTCTAGTGGTTAGA CCT C PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1668214..1668296 26863196 MeRIP-seq:(Medium) rs1037618760 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22209171,Human_RBP_ID_23712252 RMVar_hsa_circ_17614,RMVar_hsa_circ_89177,RMVar_hsa_circ_94611,RMVar_hsa_circ_97701,RMVar_hsa_circ_181077,RMVar_hsa_circ_87281,RMVar_hsa_circ_181079,RMVar_hsa_circ_181080,RMVar_hsa_circ_181078,RMVar_hsa_circ_103958,RMVar_hsa_circ_181082,RMVar_hsa_circ_123282,RMVar_hsa_circ_181083,RMVar_hsa_circ_122485,RMVar_hsa_circ_112343,RMVar_hsa_circ_79198,RMVar_hsa_circ_181088,RMVar_hsa_circ_181090,RMVar_hsa_circ_88992,RMVar_hsa_circ_181089,RMVar_hsa_circ_77570,RMVar_hsa_circ_97043,RMVar_hsa_circ_181091,RMVar_hsa_circ_181092,RMVar_hsa_circ_181096,RMVar_hsa_circ_81865,RMVar_hsa_circ_181098,RMVar_hsa_circ_77208,RMVar_hsa_circ_181097,RMVar_hsa_circ_116752,RMVar_hsa_circ_181102,RMVar_hsa_circ_105934,RMVar_hsa_circ_108793,RMVar_hsa_circ_181104,RMVar_hsa_circ_93529,RMVar_hsa_circ_181103,RMVar_hsa_circ_181101,RMVar_hsa_circ_97823,RMVar_hsa_circ_181106 103847 RMVar_ID_103847 Human_SNP_ID_614775912 m1A Human chr17 - 1669757 1669757 1669757 CTTGGAACCAAGGCCTTCAGGAACACGTGTCCAGAATTGGGGTGATGCTGAGCAGTGTCAGTTGC CTTGGAACCAAGGCCTTCAGGAACACGTGTCCGGAATTGGGGTGATGCTGAGCAGTGTCAGTTGC T C PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1669755..1669993 26863196 MeRIP-seq:(Medium) rs1469933215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12897237 RMVar_hsa_circ_17614,RMVar_hsa_circ_89177,RMVar_hsa_circ_94611,RMVar_hsa_circ_97701,RMVar_hsa_circ_181077,RMVar_hsa_circ_87281,RMVar_hsa_circ_181079,RMVar_hsa_circ_181080,RMVar_hsa_circ_181078,RMVar_hsa_circ_103958,RMVar_hsa_circ_181082,RMVar_hsa_circ_123282,RMVar_hsa_circ_181083,RMVar_hsa_circ_122485,RMVar_hsa_circ_112343,RMVar_hsa_circ_79198,RMVar_hsa_circ_181088,RMVar_hsa_circ_181090,RMVar_hsa_circ_88992,RMVar_hsa_circ_181089,RMVar_hsa_circ_77570,RMVar_hsa_circ_97043,RMVar_hsa_circ_181091,RMVar_hsa_circ_181092,RMVar_hsa_circ_181096,RMVar_hsa_circ_81865,RMVar_hsa_circ_181098,RMVar_hsa_circ_77208,RMVar_hsa_circ_181097,RMVar_hsa_circ_116752,RMVar_hsa_circ_181102,RMVar_hsa_circ_105934,RMVar_hsa_circ_108793,RMVar_hsa_circ_181104,RMVar_hsa_circ_93529,RMVar_hsa_circ_181103,RMVar_hsa_circ_181101,RMVar_hsa_circ_97823,RMVar_hsa_circ_181106 103848 RMVar_ID_103848 Human_SNP_ID_614777044 m1A Human chr17 - 1673513 1673513 1673513 ATCAAGAACCGCTTGCCACGGTCAGTGACTACAGTTCAGTGGGAGAACAGCTTCGTGTCTGTGTA ATCAAGAACCGCTTGCCACGGTCAGTGACTACGGTTCAGTGGGAGAACAGCTTCGTGTCTGTGTA T C PRPF8 Ensembl:ENSG00000174231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1673339..1673534 26863196 MeRIP-seq:(Medium) rs776258501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766261,Human_RBP_ID_1006305,Human_RBP_ID_1528178,Human_RBP_ID_1849366,Human_RBP_ID_3513015,Human_RBP_ID_4406885,Human_RBP_ID_6561848,Human_RBP_ID_8813291,Human_RBP_ID_9257677,Human_RBP_ID_9288601,Human_RBP_ID_12897366,Human_RBP_ID_17489106,Human_RBP_ID_18689580,Human_RBP_ID_22061897,Human_RBP_ID_22444177,Human_RBP_ID_24532139,Human_RBP_ID_26330992,Human_RBP_ID_26811777 Human_Splice_Rec_1758440,Human_Splice_Rec_1758522 Human_miRNA_ID_2868570 RMVar_hsa_circ_17614,RMVar_hsa_circ_89177,RMVar_hsa_circ_94611,RMVar_hsa_circ_97701,RMVar_hsa_circ_181077,RMVar_hsa_circ_87281,RMVar_hsa_circ_181079,RMVar_hsa_circ_181080,RMVar_hsa_circ_181078,RMVar_hsa_circ_123282,RMVar_hsa_circ_181083,RMVar_hsa_circ_122485,RMVar_hsa_circ_112343,RMVar_hsa_circ_79198,RMVar_hsa_circ_181090,RMVar_hsa_circ_181089,RMVar_hsa_circ_77570,RMVar_hsa_circ_97043,RMVar_hsa_circ_181091,RMVar_hsa_circ_181092,RMVar_hsa_circ_181096,RMVar_hsa_circ_81865,RMVar_hsa_circ_181098,RMVar_hsa_circ_77208,RMVar_hsa_circ_181097,RMVar_hsa_circ_116752,RMVar_hsa_circ_181102,RMVar_hsa_circ_105934,RMVar_hsa_circ_108793,RMVar_hsa_circ_181104,RMVar_hsa_circ_93529,RMVar_hsa_circ_181103,RMVar_hsa_circ_181101,RMVar_hsa_circ_21043,RMVar_hsa_circ_95499,RMVar_hsa_circ_97823,RMVar_hsa_circ_181106,RMVar_hsa_circ_78520,RMVar_hsa_circ_79862,RMVar_hsa_circ_181108,RMVar_hsa_circ_181109,RMVar_hsa_circ_82761,RMVar_hsa_circ_181110,RMVar_hsa_circ_181111 103849 RMVar_ID_103849 Human_SNP_ID_614778939 m1A Human chr17 + 1679409 1679409 1679409 CACAGGCTGCCCGGCAGGACAATGCTCCCGATACCTGGAAAAATAAGCCCACCAGAGTTTGGCCA CACAGGCTGCCCGGCAGGACAATGCTCCCGATGCCTGGAAAAATAAGCCCACCAGAGTTTGGCCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1679401..1679425 26863196 MeRIP-seq:(Medium) rs762948630 Functional Loss SNV dbSNP153 33..33 33 - - - 103850 RMVar_ID_103850 Human_SNP_ID_614780696 m1A Human chr17 + 1684425 1684425 1684425 GGGAGGGTCCCCACCCGCCTGCGCGCGCGCACACCCGCCCCGCCTCCGGCCCGCGCGCCGCTCCA GGGAGGGTCCCCACCCGCCTGCGCGCGCGCACCCCCGCCCCGCCTCCGGCCCGCGCGCCGCTCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:1684424..1684575;chr17:1684424..1684600 26863196 MeRIP-seq:(Medium) rs751976476 Functional Loss SNV dbSNP153 33..33 33 - - - 103851 RMVar_ID_103851 Human_SNP_ID_614780727 m1A Human chr17 - 1684454 1684454 1684454 AGCTGCAGGAGAAAGGTGAGGCGAGAGTGTGGAGCGGCGCGCGGGCCGGAGGCGGGGCGGGTGTG AGCTGCAGGAGAAAGGTGAGGCGAGAGTGTGGTGCGGCGCGCGGGCCGGAGGCGGGGCGGGTGTG T A PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1684451..1684600 26863196 MeRIP-seq:(Medium) rs571573436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97701,RMVar_hsa_circ_181080,RMVar_hsa_circ_122485,RMVar_hsa_circ_181090,RMVar_hsa_circ_113651,RMVar_hsa_circ_181126 103852 RMVar_ID_103852 Human_SNP_ID_614780728 m1A Human chr17 - 1684454 1684454 1684454 AGCTGCAGGAGAAAGGTGAGGCGAGAGTGTGGAGCGGCGCGCGGGCCGGAGGCGGGGCGGGTGTG AGCTGCAGGAGAAAGGTGAGGCGAGAGTGTGGCGCGGCGCGCGGGCCGGAGGCGGGGCGGGTGTG T G PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1684451..1684600 26863196 MeRIP-seq:(Medium) rs571573436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97701,RMVar_hsa_circ_181080,RMVar_hsa_circ_122485,RMVar_hsa_circ_181090,RMVar_hsa_circ_113651,RMVar_hsa_circ_181126 103853 RMVar_ID_103853 Human_SNP_ID_614780783 m1A Human chr17 - 1684548 1684548 1684548 TCTCCGGATATGGCCGGAGTGTTTCCTTATCGAGGGCCGGGTAACCCGGTGCCTGGCCCTCTAGC TCTCCGGATATGGCCGGAGTGTTTCCTTATCGGGGGCCGGGTAACCCGGTGCCTGGCCCTCTAGC T C PRPF8 Ensembl:ENSG00000174231 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1684451..1684625 26863410 MeRIP-seq:(Medium) rs1199189934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236804,Human_RBP_ID_764098,Human_RBP_ID_1006346,Human_RBP_ID_1367162,Human_RBP_ID_1528282,Human_RBP_ID_4407066,Human_RBP_ID_5365875,Human_RBP_ID_5419815,Human_RBP_ID_5466105,Human_RBP_ID_5496510,Human_RBP_ID_8444836,Human_RBP_ID_8813416,Human_RBP_ID_9257282,Human_RBP_ID_9286758,Human_RBP_ID_17258073,Human_RBP_ID_17691277,Human_RBP_ID_17885710,Human_RBP_ID_18438413,Human_RBP_ID_18689664,Human_RBP_ID_27249860,Human_RBP_ID_27661917 Human_Splice_Rec_1758398,Human_Splice_Rec_1758399,Human_Splice_Rec_1758481,Human_Splice_Rec_1758599,Human_Splice_Rec_1758650,Human_Splice_Rec_1758651 Human_miRNA_ID_2582346,Human_miRNA_ID_3115218 RMVar_hsa_circ_97701,RMVar_hsa_circ_181080,RMVar_hsa_circ_122485,RMVar_hsa_circ_181090,RMVar_hsa_circ_113651,RMVar_hsa_circ_181126 103854 RMVar_ID_103854 Human_SNP_ID_614780789 m1A Human chr17 + 1684572 1684572 1684572 CCCGGCCCTCGATAAGGAAACACTCCGGCCATATCCGGAGAATCTGGGGAGCGGCGGGATAGAAA CCCGGCCCTCGATAAGGAAACACTCCGGCCATGTCCGGAGAATCTGGGGAGCGGCGGGATAGAAA A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:1684476..1684625 26863410 MeRIP-seq:(Medium) rs1170956673 Functional Loss SNV dbSNP153 33..33 33 - - - 103855 RMVar_ID_103855 Human_SNP_ID_614780858 m1A Human chr17 + 1684733 1684733 1684733 GCCCGGCCTAACCCCTTCGGTCACTCGGCCCGACCCGACCACGCCTCCCGCAGCCCGGCCTTAAA GCCCGGCCTAACCCCTTCGGTCACTCGGCCCGTCCCGACCACGCCTCCCGCAGCCCGGCCTTAAA A T AC130343.2 Ensembl:ENSG00000277597 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1684725..1684850 26863410 MeRIP-seq:(Medium) rs538396001 Functional Loss SNV dbSNP153 33..33 33 - - - 103856 RMVar_ID_103856 Human_SNP_ID_614780894 m1A Human chr17 + 1684798 1684798 1684798 CGCCTGCCACGCACCCCACAGGCCCTCACACAAGAGGCCGCTTTCCCCGCAGCGCAATGGCGGCC CGCCTGCCACGCACCCCACAGGCCCTCACACAGGAGGCCGCTTTCCCCGCAGCGCAATGGCGGCC A G AC130343.2 Ensembl:ENSG00000277597 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:1684451..1684875 26863196 MeRIP-seq:(Medium) rs886052620 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_645 103857 RMVar_ID_103857 Human_SNP_ID_614791023 m1A Human chr17 - 1713769 1713769 1713769 GCAAGTTGGAGAGCCTTTGCCCAGATTGGCCCAGCAAGGAGCGGTTTTAGATTAGAGACACTGGC GCAAGTTGGAGAGCCTTTGCCCAGATTGGCCCGGCAAGGAGCGGTTTTAGATTAGAGACACTGGC T C MIR22HG Ensembl:ENSG00000186594 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1713720..1713861 26863196 MeRIP-seq:(Medium) rs1225854609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5580066,Human_RBP_ID_12901896 Human_Splice_Rec_1758663,Human_Splice_Rec_1758683,Human_Splice_Rec_1758699,Human_Splice_Rec_1758707,Human_Splice_Rec_1758725,Human_Splice_Rec_1758731,Human_Splice_Rec_1758735,Human_Splice_Rec_1758741,Human_Splice_Rec_1758747 103858 RMVar_ID_103858 Human_SNP_ID_614794864 m1A Human chr17 - 1725812 1725812 1725812 AAGCTTCTCATCCACTGCGATGTGATACAAAGACAGGGCCCCACACGCCAGCCCCTGGCGGTGAC AAGCTTCTCATCCACTGCGATGTGATACAAAGGCAGGGCCCCACACGCCAGCCCCTGGCGGTGAC T C AC130343.1 Ensembl:ENSG00000262791 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1725775..1725918 26863196 MeRIP-seq:(Medium) rs1325465236 Functional Loss SNV dbSNP153 33..33 33 - - - 103859 RMVar_ID_103859 Human_SNP_ID_614794876 m1A Human chr17 - 1725843 1725843 1725843 AAGCACTCAGGTCCAGTCGCAGCTCGCTGCAAAGCTTCTCATCCACTGCGATGTGATACAAAGAC AAGCACTCAGGTCCAGTCGCAGCTCGCTGCAAGGCTTCTCATCCACTGCGATGTGATACAAAGAC T C AC130343.1 Ensembl:ENSG00000262791 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1725798..1725913 26863196 MeRIP-seq:(Medium) rs1261197398 Functional Loss SNV dbSNP153 33..33 33 - - - 103860 RMVar_ID_103860 Human_SNP_ID_614795888 m1A Human chr17 + 1728404 1728404 1728404 GATCAGGTGACAGCAGCCAGGACTTGAAGCAAAGCGAGGGCTCCGAGGAGGAAGAGGAGGAGGAG GATCAGGTGACAGCAGCCAGGACTTGAAGCAACGCGAGGGCTCCGAGGAGGAAGAGGAGGAGGAG A C WDR81 Ensembl:ENSG00000167716 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1728308..1728575 26863196 MeRIP-seq:(Medium) rs1162506100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112600,RMVar_hsa_circ_181130 103861 RMVar_ID_103861 Human_SNP_ID_614795912 m1A Human chr17 - 1728443 1728443 1728443 CTGCTCCCCCTCCTCCTCCTCTAGCACCACGCAGCTGTCCTCCTCCTCCTCTTCCTCCTCGGAGC CTGCTCCCCCTCCTCCTCCTCTAGCACCACGCTGCTGTCCTCCTCCTCCTCTTCCTCCTCGGAGC T A AC130343.1 Ensembl:ENSG00000262791 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1728202..1728602 26863196 MeRIP-seq:(Medium) rs1002949957 Functional Loss SNV dbSNP153 33..33 33 - - - 103862 RMVar_ID_103862 Human_SNP_ID_614798569 m1A Human chr17 - 1735964 1735964 1735964 CTCACACTCCCCAAGGCCCTGCCCACCACCCAAGCCCACACAGCAGGAAGGCCTGAGCCTCTGAC CTCACACTCCCCAAGGCCCTGCCCACCACCCAGGCCCACACAGCAGGAAGGCCTGAGCCTCTGAC T C AC130343.1 Ensembl:ENSG00000262791 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:1735939..1736087 26863196 MeRIP-seq:(Medium) rs957872396 Functional Loss SNV dbSNP153 33..33 33 - - - 103863 RMVar_ID_103863 Human_SNP_ID_614800307 m1A Human chr17 - 1741787 1741787 1741787 ACTGTCCTGCGCCTCACTCCCTGCATCGGGCCACTTCCCACCCTCACTGTCCTGCTCCTCACTCC ACTGTCCTGCGCCTCACTCCCTGCATCGGGCCGCTTCCCACCCTCACTGTCCTGCTCCTCACTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1741736..1741817 26863196 MeRIP-seq:(Medium) rs1311617312 Functional Loss SNV dbSNP153 33..33 33 - - - 103864 RMVar_ID_103864 Human_SNP_ID_614800308 m1A Human chr17 - 1741787 1741787 1741787 ACTGTCCTGCGCCTCACTCCCTGCATCGGGCCACTTCCCACCCTCACTGTCCTGCTCCTCACTCC ACTGTCCTGCGCCTCACTCCCTGCATCGGGCCCCTTCCCACCCTCACTGTCCTGCTCCTCACTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1741736..1741817 26863196 MeRIP-seq:(Medium) rs1311617312 Functional Loss SNV dbSNP153 33..33 33 - - - 103865 RMVar_ID_103865 Human_SNP_ID_614800312 m1A Human chr17 + 1741794 1741794 1741794 GGAGCAGGACAGTGAGGGTGGGAAGTGGCCCGATGCAGGGAGTGAGGCGCAGGACAGTGAGGGTG GGAGCAGGACAGTGAGGGTGGGAAGTGGCCCGTTGCAGGGAGTGAGGCGCAGGACAGTGAGGGTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:1741704..1742183 26863196 MeRIP-seq:(Medium) rs1227133456 Functional Loss SNV dbSNP153 33..33 33 - - - 103866 RMVar_ID_103866 Human_SNP_ID_614809402 m1A Human chr17 + 1770026 1770026 1770026 CCAACGTGCTCCTGTCTCCTCTCAGTGTGGCCACGGCCCTCTCGGCCCTCTCGCTGGGTGAGTGC CCAACGTGCTCCTGTCTCCTCTCAGTGTGGCCTCGGCCCTCTCGGCCCTCTCGCTGGGTGAGTGC A T SERPINF1 Ensembl:ENSG00000132386 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1769910..1770534 32194978 MeRIP-seq:(Medium) rs373146540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821217,Human_RBP_ID_22443325,Human_RBP_ID_22760668,Human_RBP_ID_26811789 Human_Splice_Rec_1758981,Human_Splice_Rec_1758987,Human_Splice_Rec_1759001,Human_Splice_Rec_1759009,Human_Splice_Rec_1759015,Human_Splice_Rec_1759031,Human_Splice_Rec_1759037 RMVar_hsa_circ_64660,RMVar_hsa_circ_86136,RMVar_hsa_circ_318222,RMVar_hsa_circ_181144,RMVar_hsa_circ_286577 103867 RMVar_ID_103867 Human_SNP_ID_614812032 m1A Human chr17 - 1777206 1777206 1777206 GGTTTGCCTGTGATCTTGCTAAAGTCTGGTGAATCAAACAAGGATTGCAGCTCTGTAGAGATGGA GGTTTGCCTGTGATCTTGCTAAAGTCTGGTGACTCAAACAAGGATTGCAGCTCTGTAGAGATGGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1776585..1777228 32194978 MeRIP-seq:(Medium) rs767394712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18690132 103868 RMVar_ID_103868 Human_SNP_ID_614813084 m1A Human chr17 + 1780523 1780523 1780523 ACAGGTGTGAGCCTCTACACTGGGCCTGCAGAACCTACACAGAATCCGCACCTGGTCTGCAGAAC ACAGGTGTGAGCCTCTACACTGGGCCTGCAGAGCCTACACAGAATCCGCACCTGGTCTGCAGAAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:1780473..1780770 26863196 MeRIP-seq:(Medium) rs766486664 Functional Loss SNV dbSNP153 33..33 33 - - - 103869 RMVar_ID_103869 Human_SNP_ID_614813087 m1A Human chr17 - 1780535 1780535 1780535 GGTCGGGTGTGGGTTCTGCAGACCAGGTGCGGATTCTGTGTAGGTTCTGCAGGCCCAGTGTAGAG GGTCGGGTGTGGGTTCTGCAGACCAGGTGCGGGTTCTGTGTAGGTTCTGCAGGCCCAGTGTAGAG T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1780486..1780611 26863196 MeRIP-seq:(Medium) rs1433887282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237079,Human_RBP_ID_484010,Human_RBP_ID_6563932,Human_RBP_ID_9353362,Human_RBP_ID_12903753,Human_RBP_ID_23713099,Human_RBP_ID_26456978 RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 103870 RMVar_ID_103870 Human_SNP_ID_614828119 m1A Human chr17 + 1829747 1829747 1829747 GGGATACCAACCCGTGCACTCGCCAGAGACCGAGGCGAGAACGCCTCGAGAACCGCTCAGACGCG GGGATACCAACCCGTGCACTCGCCAGAGACCGCGGCGAGAACGCCTCGAGAACCGCTCAGACGCG A C RPA1 Ensembl:ENSG00000132383 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr17:1829741..1829826;chr17:1829744..1829848 26863410,26863196 MeRIP-seq:(Medium) rs1238242453 Functional Loss SNV dbSNP153 33..33 33 - - - 103871 RMVar_ID_103871 Human_SNP_ID_614828169 m1A Human chr17 - 1829836 1829836 1829836 CCGGACGCGGTGCGGGGCGGAGCGGGGCGCCAAGGGGCGCGCCAGGAGCTGCGCGGGCGCTGGGA CCGGACGCGGTGCGGGGCGGAGCGGGGCGCCAGGGGGCGCGCCAGGAGCTGCGCGGGCGCTGGGA T C SMYD4 Ensembl:ENSG00000186532 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:1829732..1829867 26863196 MeRIP-seq:(Medium) rs940237048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4408521,Human_RBP_ID_18419819 103872 RMVar_ID_103872 Human_SNP_ID_614828333 m1A Human chr17 + 1830094 1830094 1830094 GGGGTCCGCGGGGAAGTCTTGGCGGTGGAGCCATGGTCGGCCAACTGAGCGAGGGGGCCATTGCG GGGGTCCGCGGGGAAGTCTTGGCGGTGGAGCCGTGGTCGGCCAACTGAGCGAGGGGGCCATTGCG A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:1830001..1830202 26863196 MeRIP-seq:(Medium) rs1227945482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484214,Human_RBP_ID_1238467,Human_RBP_ID_3951601,Human_RBP_ID_4464226,Human_RBP_ID_8445509,Human_RBP_ID_8824297,Human_RBP_ID_9288664,Human_RBP_ID_9353293,Human_RBP_ID_18419507,Human_RBP_ID_22959714 Human_Splice_Rec_1759123,Human_Splice_Rec_1759135 RMVar_hsa_circ_79735,RMVar_hsa_circ_85244,RMVar_hsa_circ_181159,RMVar_hsa_circ_181160 103873 RMVar_ID_103873 Human_SNP_ID_614828363 m1A Human chr17 + 1830121 1830121 1830121 GAGCCATGGTCGGCCAACTGAGCGAGGGGGCCATTGCGGTGAGGAGGTGCCGGGGGCTGGGCCGG GAGCCATGGTCGGCCAACTGAGCGAGGGGGCCGTTGCGGTGAGGAGGTGCCGGGGGCTGGGCCGG A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1830026..1830175 26863410 MeRIP-seq:(Medium) rs1420099438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238467,Human_RBP_ID_3951601,Human_RBP_ID_4464226,Human_RBP_ID_5365905,Human_RBP_ID_8824297,Human_RBP_ID_9353363,Human_RBP_ID_18419507,Human_RBP_ID_19080909,Human_RBP_ID_22959714 Human_Splice_Rec_1759123,Human_Splice_Rec_1759135 RMVar_hsa_circ_79735,RMVar_hsa_circ_85244,RMVar_hsa_circ_181159,RMVar_hsa_circ_181160 103874 RMVar_ID_103874 Human_SNP_ID_614831920 m1A Human chr17 - 1842746 1842746 1842746 GTGAGATACGCACTCAAATCATGATGAAAATGACATGTTTTTATAGTTGGTATTTGGAATATATA GTGAGATACGCACTCAAATCATGATGAAAATGGCATGTTTTTATAGTTGGTATTTGGAATATATA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1842744..1842914 26863196 MeRIP-seq:(Medium) rs1567802405 Functional Loss SNV dbSNP153 33..33 33 - - - 103875 RMVar_ID_103875 Human_SNP_ID_614835589 m1A Human chr17 - 1856102 1856102 1856102 GCAGGCTGGTCTTGAACTCCCAAGCGCAAGCGATCGGCTTGCCTCGTTCTCCCAAGGTGTTGGGA GCAGGCTGGTCTTGAACTCCCAAGCGCAAGCGGTCGGCTTGCCTCGTTCTCCCAAGGTGTTGGGA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:1856092..1856176 26863410 MeRIP-seq:(Medium) rs952555502 Functional Loss SNV dbSNP153 33..33 33 - - - 103876 RMVar_ID_103876 Human_SNP_ID_614842194 m1A Human chr17 + 1880596 1880596 1880596 AGACAGCCCGTGTTGGCTATCAAAGGAGCCCGAGTCTCTGATTTCGGTGGACGGAGCCTCTCCGT AGACAGCCCGTGTTGGCTATCAAAGGAGCCCGCGTCTCTGATTTCGGTGGACGGAGCCTCTCCGT A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cells, overexperss TRMT6;HTR8/Svneo,Normoxia chr17:1880546..1880647 29072297,32194978 m1A-MAP:(High) rs1207404948 Functional Loss SNV dbSNP153 33..33 33 - - - 103877 RMVar_ID_103877 Human_SNP_ID_614846899 m1A Human chr17 - 1897264 1897264 1897264 TTAGTCCACCATCAAGAGCCTCTGCACTGTGTAGCTAACATGGGATCGTCACACGGAGGTGGGAG TTAGTCCACCATCAAGAGCCTCTGCACTGTGTGGCTAACATGGGATCGTCACACGGAGGTGGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1897076..1897550 32194978 MeRIP-seq:(Medium) rs948306052 Functional Loss SNV dbSNP153 33..33 33 - - - 103878 RMVar_ID_103878 Human_SNP_ID_614886671 m1A Human chr17 + 2030204 2030204 2030204 GGCGGCGCTGGTCGTATCCGGGGCAGCGGAGCAGGGCGGCCGAGACGGCCCTGGCAGAGGTGGGT GGCGGCGCTGGTCGTATCCGGGGCAGCGGAGCGGGGCGGCCGAGACGGCCCTGGCAGAGGTGGGT A G DPH1 Ensembl:ENSG00000108963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:2030151..2030276;chr17:2030151..2030284;chr17:2030151..2030291 26863196 MeRIP-seq:(Medium) rs375040102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237711,Human_RBP_ID_18419508 Human_Splice_Rec_1759215,Human_Splice_Rec_1759239,Human_Splice_Rec_1759263,Human_Splice_Rec_1759285,Human_Splice_Rec_1759309,Human_Splice_Rec_1759317 103879 RMVar_ID_103879 Human_SNP_ID_614887493 m1A Human chr17 + 2033452 2033452 2033452 CAGGCCCTGAAAAGGGATCCCTATTCCATCTCAATCTGGCTTCAGCCAAAGACAGACACCAACTC CAGGCCCTGAAAAGGGATCCCTATTCCATCTCGATCTGGCTTCAGCCAAAGACAGACACCAACTC A G DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:2033446..2033625 26863410 MeRIP-seq:(Medium) rs777878153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17886745 103880 RMVar_ID_103880 Human_SNP_ID_614887494 m1A Human chr17 + 2033452 2033452 2033452 CAGGCCCTGAAAAGGGATCCCTATTCCATCTCAATCTGGCTTCAGCCAAAGACAGACACCAACTC CAGGCCCTGAAAAGGGATCCCTATTCCATCTCTATCTGGCTTCAGCCAAAGACAGACACCAACTC A T DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:2033446..2033625 26863410 MeRIP-seq:(Medium) rs777878153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17886745 103881 RMVar_ID_103881 Human_SNP_ID_614887548 m1A Human chr17 + 2033556 2033556 2033556 CGTGGCCAATCAGATCCCCCCTGAGATCCTGAAGAACCCTCAGCTGCAGGCAGCAATCCGGGTCC CGTGGCCAATCAGATCCCCCCTGAGATCCTGACGAACCCTCAGCTGCAGGCAGCAATCCGGGTCC A C DPH1 Ensembl:ENSG00000108963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:2033473..2033625;chr17:2033481..2033584 26863196 MeRIP-seq:(Medium) rs181803178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1850671,Human_RBP_ID_8446234,Human_RBP_ID_12919184,Human_RBP_ID_18419820 Human_Splice_Rec_1759216,Human_Splice_Rec_1759240,Human_Splice_Rec_1759264,Human_Splice_Rec_1759286,Human_Splice_Rec_1759310,Human_Splice_Rec_1759318 RMVar_hsa_circ_2689 103882 RMVar_ID_103882 Human_SNP_ID_614888732 m1A Human chr17 + 2036635 2036635 2036635 CTCCTGGACTCTCTCCGCCTCACCTTTCCCCCAGCCACTGCCCTTGCCCTGGTCAGCACCATTCA CTCCTGGACTCTCTCCGCCTCACCTTTCCCCCGGCCACTGCCCTTGCCCTGGTCAGCACCATTCA A G DPH1 Ensembl:ENSG00000108963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2036585..2036693 26863196 MeRIP-seq:(Medium) rs758268406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27460126 Human_Splice_Rec_1759223,Human_Splice_Rec_1759247,Human_Splice_Rec_1759269,Human_Splice_Rec_1759293,Human_Splice_Rec_1759315,Human_Splice_Rec_1759325,Human_Splice_Rec_1759333,Human_Splice_Rec_1759353,Human_Splice_Rec_1759361 Human_miRNA_ID_1012222,Human_miRNA_ID_1294237,Human_miRNA_ID_1298218,Human_miRNA_ID_1357702 RMVar_hsa_circ_2689,RMVar_hsa_circ_40429 103883 RMVar_ID_103883 Human_SNP_ID_614890804 m1A Human chr17 - 2042133 2042133 2042133 CGAGCTCGGCGCGACCCCGCAGCGCCTTCCTCAGCGCCCCGGTCTTCTCACGGAAGCCCCGCTCG CGAGCTCGGCGCGACCCCGCAGCGCCTTCCTCGGCGCCCCGGTCTTCTCACGGAAGCCCCGCTCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2042083..2042167 26863196 MeRIP-seq:(Medium) rs748130733 Functional Loss SNV dbSNP153 33..33 33 - - - 103884 RMVar_ID_103884 Human_SNP_ID_614891112 m1A Human chr17 - 2042704 2042704 2042704 GTGCCTGTGCCACCATCCCCAGTGATTCCTCCAGGCCCCTGCAGACGGCGGGCTCTTCCAATGCG GTGCCTGTGCCACCATCCCCAGTGATTCCTCCTGGCCCCTGCAGACGGCGGGCTCTTCCAATGCG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2042605..2042750 26863196 MeRIP-seq:(Medium) rs142574497 Functional Loss SNV dbSNP153 33..33 33 - - - 103885 RMVar_ID_103885 Human_SNP_ID_614891251 m1A Human chr17 + 2042959 2042959 2042959 GCCTTCGCTCCATGTTTTTGGGGACACTGACAAAGTCATCCCCTCTCAGGAGAGTGTGCAACTGG GCCTTCGCTCCATGTTTTTGGGGACACTGACAGAGTCATCCCCTCTCAGGAGAGTGTGCAACTGG A G OVCA2,DPH1 Ensembl:ENSG00000262664,Ensembl:ENSG00000108963 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:2042851..2043430 32194978 MeRIP-seq:(Medium) rs750970512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767670,Human_RBP_ID_23714979 103886 RMVar_ID_103886 Human_SNP_ID_614893855 m1A Human chr17 - 2050923 2050923 2050923 GCCCGCGCAGCACCTGCCGGCGCCCGATGGACACGCAGCTACTTCGGAGGAGCATCGAGTGGAGG GCCCGCGCAGCACCTGCCGGCGCCCGATGGACTCGCAGCTACTTCGGAGGAGCATCGAGTGGAGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2050872..2050963 26863196 MeRIP-seq:(Medium) rs1439332214 Functional Loss SNV dbSNP153 33..33 33 - - - 103887 RMVar_ID_103887 Human_SNP_ID_614894311 m1A Human chr17 + 2052312 2052312 2052312 GGATGGGGAGGGCTGTGCAAGGCATGGCCGGAAGAGCGGGGCAGGGAGAGAAAGGTCGAAGAGTG GGATGGGGAGGGCTGTGCAAGGCATGGCCGGAGGAGCGGGGCAGGGAGAGAAAGGTCGAAGAGTG A G RF00017-156,lnc-HIC1-3 RNACentral:URS000091874B,RNACentral:URS0000D5C34B SRP RNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:2051564..2052398;chr17:2052181..2052400 26863196 MeRIP-seq:(Medium) rs561354721 Functional Loss SNV dbSNP153 33..33 33 - - - 103888 RMVar_ID_103888 Human_SNP_ID_614895237 m1A Human chr17 + 2055149 2055149 2055149 ACGCGGGGAGGACGGACCAGCAGGACAGACCGACCGGGGGCCCGGCGGGCGGAGGGCAGCGCAGC ACGCGGGGAGGACGGACCAGCAGGACAGACCGGCCGGGGGCCCGGCGGGCGGAGGGCAGCGCAGC A G HIC1 Ensembl:ENSG00000177374 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2055108..2055248 26863196 MeRIP-seq:(Medium) rs1226500784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1759421,Human_Splice_Rec_1759425,Human_Splice_Rec_1759429,Human_Splice_Rec_1759431,Human_Splice_Rec_1759433 RMVar_hsa_circ_81667,RMVar_hsa_circ_181196 103889 RMVar_ID_103889 Human_SNP_ID_614895326 m1A Human chr17 + 2055392 2055392 2055392 TCAGGGCTCCGGGTGTCGTCCCTTTCGGACTCAGGACCACCGGGCCGCGGCTCCGCGCCGGGTTC TCAGGGCTCCGGGTGTCGTCCCTTTCGGACTCGGGACCACCGGGCCGCGGCTCCGCGCCGGGTTC A G HIC1 Ensembl:ENSG00000177374 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2055276..2055513 26863196 MeRIP-seq:(Medium) rs1363499403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81667,RMVar_hsa_circ_181196 103890 RMVar_ID_103890 Human_SNP_ID_614897812 m1A Human chr17 - 2061534 2061534 2061534 CGTGTGAAGGCGCTCACAAGGAATGTTCCTGTACGGGACATCCCAGCCTTCCTCACGTGGGCCCA CGTGTGAAGGCGCTCACAAGGAATGTTCCTGTGCGGGACATCCCAGCCTTCCTCACGTGGGCCCA T C SMG6 Ensembl:ENSG00000070366 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2061201..2061550 32194978 MeRIP-seq:(Medium) rs762566596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1759472,Human_Splice_Rec_1759484,Human_Splice_Rec_1759506,Human_Splice_Rec_1759516,Human_Splice_Rec_1759526,Human_Splice_Rec_1759546,Human_Splice_Rec_1759552,Human_Splice_Rec_1759560 RMVar_hsa_circ_90111,RMVar_hsa_circ_103487,RMVar_hsa_circ_119061,RMVar_hsa_circ_100757,RMVar_hsa_circ_181197,RMVar_hsa_circ_181199,RMVar_hsa_circ_181200,RMVar_hsa_circ_181198 103891 RMVar_ID_103891 Human_SNP_ID_614903466 m1A Human chr17 - 2081900 2081900 2081900 TTTGAGGAAGATTCAGAGGCTGAAGGCAGCGGAGGCGAGGATGACATCAGGGAGCTTCGGGCCAA TTTGAGGAAGATTCAGAGGCTGAAGGCAGCGGCGGCGAGGATGACATCAGGGAGCTTCGGGCCAA T G SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2081849..2085794 26863196 MeRIP-seq:(Medium) rs928540142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18989917,Human_RBP_ID_26456987 Human_Splice_Rec_1759464,Human_Splice_Rec_1759465,Human_Splice_Rec_1759476,Human_Splice_Rec_1759477,Human_Splice_Rec_1759498,Human_Splice_Rec_1759499,Human_Splice_Rec_1759508,Human_Splice_Rec_1759509,Human_Splice_Rec_1759518,Human_Splice_Rec_1759519,Human_Splice_Rec_1759538,Human_Splice_Rec_1759539,Human_Splice_Rec_1759566,Human_Splice_Rec_1759567,Human_Splice_Rec_1759572 RMVar_hsa_circ_9933,RMVar_hsa_circ_90111,RMVar_hsa_circ_103487,RMVar_hsa_circ_119061,RMVar_hsa_circ_100757,RMVar_hsa_circ_181197,RMVar_hsa_circ_181199,RMVar_hsa_circ_181200,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_20465,RMVar_hsa_circ_374509,RMVar_hsa_circ_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181202,RMVar_hsa_circ_181203,RMVar_hsa_circ_315746 103892 RMVar_ID_103892 Human_SNP_ID_614903485 m1A Human chr17 - 2081949 2081949 2081949 TCCTGGTCGGCTCCACCACCCAAAGGAGGAGGATGTGGTGATTGAAGACTTTGAGGAAGATTCAG TCCTGGTCGGCTCCACCACCCAAAGGAGGAGGTTGTGGTGATTGAAGACTTTGAGGAAGATTCAG T A SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2081898..2082009 26863196 MeRIP-seq:(Medium) rs769548238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4410846,Human_RBP_ID_22655659 Human_Splice_Rec_1759464,Human_Splice_Rec_1759476,Human_Splice_Rec_1759498,Human_Splice_Rec_1759508,Human_Splice_Rec_1759518,Human_Splice_Rec_1759538,Human_Splice_Rec_1759566,Human_Splice_Rec_1759572 RMVar_hsa_circ_9933,RMVar_hsa_circ_90111,RMVar_hsa_circ_103487,RMVar_hsa_circ_119061,RMVar_hsa_circ_100757,RMVar_hsa_circ_181197,RMVar_hsa_circ_181199,RMVar_hsa_circ_181200,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_20465,RMVar_hsa_circ_374509,RMVar_hsa_circ_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181202,RMVar_hsa_circ_181203,RMVar_hsa_circ_315746 103893 RMVar_ID_103893 Human_SNP_ID_614904405 m1A Human chr17 - 2085765 2085765 2085765 GTCAGTGGCACCCGTCCCAGACACCATGGGAAAGGAAATGGGAAGCCAAGAGGGAACACGACTGG GTCAGTGGCACCCGTCCCAGACACCATGGGAATGGAAATGGGAAGCCAAGAGGGAACACGACTGG T A SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2085678..2085764 26863196 MeRIP-seq:(Medium) rs1410793851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1759463,Human_Splice_Rec_1759475,Human_Splice_Rec_1759497,Human_Splice_Rec_1759537,Human_Splice_Rec_1759565,Human_Splice_Rec_1759571 RMVar_hsa_circ_9933,RMVar_hsa_circ_90111,RMVar_hsa_circ_119061,RMVar_hsa_circ_100757,RMVar_hsa_circ_181197,RMVar_hsa_circ_181199,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_29492,RMVar_hsa_circ_374509,RMVar_hsa_circ_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181202,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_315746,RMVar_hsa_circ_181204 103894 RMVar_ID_103894 Human_SNP_ID_614957232 m1A Human chr17 - 2281759 2281758 2281760 TTAAGGGTAAAATTCACCCAGTGGGTGGTGTAAGCTGGGGCTAGATGTTGAAGGGTCATATGATA TTAAGGGTAAAATTCACCCAGTGGGTGGTGT__GCTGGGGCTAGATGTTGAAGGGTCATATGATA CTT C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2281757..2281905 26863196 MeRIP-seq:(Medium) rs919358878 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_90111,RMVar_hsa_circ_181197,RMVar_hsa_circ_98730,RMVar_hsa_circ_181201,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_181211,RMVar_hsa_circ_14921,RMVar_hsa_circ_344709 103895 RMVar_ID_103895 Human_SNP_ID_614962706 m1A Human chr17 - 2299922 2299922 2299922 AGCGCTGAGGGAGCTGGCCTGACGGATAATGGATGTCGCCGCCGCCGACAGGATAGGACCAAGGA AGCGCTGAGGGAGCTGGCCTGACGGATAATGGGTGTCGCCGCCGCCGACAGGATAGGACCAAGGA T C SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2299871..2300284 26863196 MeRIP-seq:(Medium) rs762196667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4411782,Human_RBP_ID_12929165 RMVar_hsa_circ_181220,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_181211,RMVar_hsa_circ_344709,RMVar_hsa_circ_338729,RMVar_hsa_circ_313403,RMVar_hsa_circ_181224,RMVar_hsa_circ_286238 103896 RMVar_ID_103896 Human_SNP_ID_614962826 m1A Human chr17 - 2300114 2300114 2300114 AGCCCAGGTGGTGGGAGAGTAGGGGCTGCAAAAGGAGAAAAAGGAAAGAGGATGGGAAAAGGGGA AGCCCAGGTGGTGGGAGAGTAGGGGCTGCAAAGGGAGAAAAAGGAAAGAGGATGGGAAAAGGGGA T C SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2299733..2300356 26863196 MeRIP-seq:(Medium) rs114525686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9422164,Human_RBP_ID_25257792 RMVar_hsa_circ_181220,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_181211,RMVar_hsa_circ_344709,RMVar_hsa_circ_338729,RMVar_hsa_circ_313403,RMVar_hsa_circ_181224,RMVar_hsa_circ_286238 103897 RMVar_ID_103897 Human_SNP_ID_614962859 m1A Human chr17 + 2300196 2300196 2300196 TGTCTGGTTTATTCGCAACTTCCTCCTTCGCAACATTTCCCCTACACTCATCTTCCTCTACTCTC TGTCTGGTTTATTCGCAACTTCCTCCTTCGCAGCATTTCCCCTACACTCATCTTCCTCTACTCTC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:2300092..2300298 26863196 MeRIP-seq:(Medium) rs760857916 Functional Loss SNV dbSNP153 33..33 33 - - - 103898 RMVar_ID_103898 Human_SNP_ID_614964120 m1A Human chr17 + 2303773 2303773 2303773 CCGTAGCGGCTCCGCCACCGCCGCGCGCAGCCAGGAAACCACCACAGACGGGCGGCGCGCGCGCT CCGTAGCGGCTCCGCCACCGCCGCGCGCAGCCCGGAAACCACCACAGACGGGCGGCGCGCGCGCT A C SRR Ensembl:ENSG00000167720 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2303722..2303817 26863196 MeRIP-seq:(Medium) rs1358960580 Functional Loss SNV dbSNP153 33..33 33 - - - 103899 RMVar_ID_103899 Human_SNP_ID_614964125 m1A Human chr17 + 2303784 2303784 2303784 CCGCCACCGCCGCGCGCAGCCAGGAAACCACCACAGACGGGCGGCGCGCGCGCTCGCCCACCTCC CCGCCACCGCCGCGCGCAGCCAGGAAACCACCCCAGACGGGCGGCGCGCGCGCTCGCCCACCTCC A C SRR Ensembl:ENSG00000167720 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2303633..2303821 26863196 MeRIP-seq:(Medium) rs1313253450 Functional Loss SNV dbSNP153 33..33 33 - - - 103900 RMVar_ID_103900 Human_SNP_ID_614964142 m1A Human chr17 - 2303805 2303805 2303805 GCAGGGGGCGGGGAAAGGCCGGGAGGTGGGCGAGCGCGCGCGCCGCCCGTCTGTGGTGGTTTCCT GCAGGGGGCGGGGAAAGGCCGGGAGGTGGGCGGGCGCGCGCGCCGCCCGTCTGTGGTGGTTTCCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2303637..2303810 26863196 MeRIP-seq:(Medium) rs959126878 Functional Loss SNV dbSNP153 33..33 33 - - - 103901 RMVar_ID_103901 Human_SNP_ID_614969952 m1A Human chr17 - 2324259 2324259 2324259 TTCCCCAAATGGACTTATGATCCATATGTACCAGAACCAGTACCCTGGCTGAAAAGTGAGATTTC TTCCCCAAATGGACTTATGATCCATATGTACCGGAACCAGTACCCTGGCTGAAAAGTGAGATTTC T C TSR1 Ensembl:ENSG00000167721 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:2324210..2324690 32194978 MeRIP-seq:(Medium) rs1394241989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485219,Human_RBP_ID_1529582,Human_RBP_ID_1851220,Human_RBP_ID_2497474,Human_RBP_ID_5143990,Human_RBP_ID_8446887,Human_RBP_ID_12929569,Human_RBP_ID_22445249,Human_RBP_ID_26956985 103902 RMVar_ID_103902 Human_SNP_ID_614972363 m1A Human chr17 - 2332353 2332353 2332353 GAAAAAACTGTAATCCTATTCTACAGGATGAGAGTAGTGAAGAAGAGGAAGAATATGAAACTATG GAAAAAACTGTAATCCTATTCTACAGGATGAGGGTAGTGAAGAAGAGGAAGAATATGAAACTATG T C TSR1 Ensembl:ENSG00000167721 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2332226..2332386 26863196 MeRIP-seq:(Medium) rs1017307683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951611,Human_RBP_ID_6570456,Human_RBP_ID_22060939,Human_RBP_ID_23716421,Human_RBP_ID_26331015,Human_RBP_ID_27812153 Human_Splice_Rec_1759706 RMVar_hsa_circ_310108,RMVar_hsa_circ_315654 103903 RMVar_ID_103903 Human_SNP_ID_614972364 m1A Human chr17 - 2332353 2332353 2332353 GAAAAAACTGTAATCCTATTCTACAGGATGAGAGTAGTGAAGAAGAGGAAGAATATGAAACTATG GAAAAAACTGTAATCCTATTCTACAGGATGAGCGTAGTGAAGAAGAGGAAGAATATGAAACTATG T G TSR1 Ensembl:ENSG00000167721 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2332226..2332386 26863196 MeRIP-seq:(Medium) rs1017307683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951611,Human_RBP_ID_6570456,Human_RBP_ID_22060939,Human_RBP_ID_23716421,Human_RBP_ID_26331015,Human_RBP_ID_27812153 Human_Splice_Rec_1759706 RMVar_hsa_circ_310108,RMVar_hsa_circ_315654 103904 RMVar_ID_103904 Human_SNP_ID_614972592 m1A Human chr17 + 2333011 2333011 2333011 AAAATCCTCATGTTCCATATCATCATATTCATATTCATCTCCTTCCCCACCACTTTGGCTGCCAC AAAATCCTCATGTTCCATATCATCATATTCATGTTCATCTCCTTCCCCACCACTTTGGCTGCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2332941..2333125 26863196 MeRIP-seq:(Medium) rs779654482 Functional Loss SNV dbSNP153 33..33 33 - - - 103905 RMVar_ID_103905 Human_SNP_ID_614973489 m1A Human chr17 - 2335700 2335700 2335700 AGGTTCTGGCAGAGAAGAGACAGCTGGGTGGCAAGGATGGCCCTCCTCATCAGGTACTGGTGGTG AGGTTCTGGCAGAGAAGAGACAGCTGGGTGGCCAGGATGGCCCTCCTCATCAGGTACTGGTGGTG T G TSR1 Ensembl:ENSG00000167721 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2335651..2335770 26863196 MeRIP-seq:(Medium) rs1166058321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238050,Human_RBP_ID_896082,Human_RBP_ID_5363454,Human_RBP_ID_6570489,Human_RBP_ID_9375066,Human_RBP_ID_17887352,Human_RBP_ID_18989927,Human_RBP_ID_22542745,Human_RBP_ID_22587438,Human_RBP_ID_22740808,Human_RBP_ID_26331022,Human_RBP_ID_26957027,Human_RBP_ID_27812156 Human_Splice_Rec_1759696,Human_Splice_Rec_1759730,Human_Splice_Rec_1759738,Human_Splice_Rec_1759744 103906 RMVar_ID_103906 Human_SNP_ID_614973635 m1A Human chr17 + 2336128 2336109 2336129 GTTCTTTTCTCACCTTCTTGCTTAGGGTTTTCAGTGCCAGACGGCCTGAATGGCAGATTAGAAGG GTTCTTTTCTCACC____________________TGCCAGACGGCCTGAATGGCAGATTAGAAGG CTTCTTGCTTAGGGTTTTCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:2336011..2336177;chr17:2336026..2336169;chr17:2336026..2336158;chr17:2336051..2336158 26863196 MeRIP-seq:(Medium) rs1424521247 Functional Loss DEL dbSNP153 15..34 33 - - - 103907 RMVar_ID_103907 Human_SNP_ID_614973703 m1A Human chr17 + 2336280 2336279 2336281 GAGACAGAAGCTCAGTCTGGGCATGAGGAAAAAGAGTTAATAACGGCCAAATAGCCCTTATTCCT GAGACAGAAGCTCAGTCTGGGCATGAGGAAAA__AGTTAATAACGGCCAAATAGCCCTTATTCCT AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2336278..2336450 26863196 MeRIP-seq:(Medium) rs1375797322 Functional Loss DEL dbSNP153 33..34 33 - - - 103908 RMVar_ID_103908 Human_SNP_ID_614973704 m1A Human chr17 + 2336280 2336280 2336280 GAGACAGAAGCTCAGTCTGGGCATGAGGAAAAAGAGTTAATAACGGCCAAATAGCCCTTATTCCT GAGACAGAAGCTCAGTCTGGGCATGAGGAAAACGAGTTAATAACGGCCAAATAGCCCTTATTCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2336278..2336450 26863196 MeRIP-seq:(Medium) rs757396301 Functional Loss SNV dbSNP153 33..33 33 - - - 103909 RMVar_ID_103909 Human_SNP_ID_614973711 m1A Human chr17 + 2336290 2336290 2336290 CTCAGTCTGGGCATGAGGAAAAAGAGTTAATAACGGCCAAATAGCCCTTATTCCTTCTACGTTAT CTCAGTCTGGGCATGAGGAAAAAGAGTTAATAGCGGCCAAATAGCCCTTATTCCTTCTACGTTAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2336289..2336425 26863196 MeRIP-seq:(Medium) rs758843215 Functional Loss SNV dbSNP153 33..33 33 - - - 103910 RMVar_ID_103910 Human_SNP_ID_614974180 m1A Human chr17 - 2337544 2337544 2337544 CCCGGCCCGCCGCCGCCGCCGCCGCCGCAGCCACTGCCCGGTGCTCGGCTCCGCAGCCATCTTCC CCCGGCCCGCCGCCGCCGCCGCCGCCGCAGCCGCTGCCCGGTGCTCGGCTCCGCAGCCATCTTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2337501..2361662 26863196 MeRIP-seq:(Medium) rs1247535073 Functional Loss SNV dbSNP153 33..33 33 - - - 103911 RMVar_ID_103911 Human_SNP_ID_614974182 m1A Human chr17 - 2337548 2337548 2337548 CGCTCCCGGCCCGCCGCCGCCGCCGCCGCCGCAGCCACTGCCCGGTGCTCGGCTCCGCAGCCATC CGCTCCCGGCCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCCGGTGCTCGGCTCCGCAGCCATC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:2337501..2337776;chr17:2337501..2337792;chr17:2337501..2343625 26863196 MeRIP-seq:(Medium) rs1305831086 Functional Loss SNV dbSNP153 33..33 33 - - - 103912 RMVar_ID_103912 Human_SNP_ID_614981099 m1A Human chr17 + 2361775 2361775 2361775 AGTGGCGGGGGAGATTTGCCACAAGGTACAGGAGCTGCAGCAACAAGCAGAGGGCAGGTGAGCCC AGTGGCGGGGGAGATTTGCCACAAGGTACAGGGGCTGCAGCAACAAGCAGAGGGCAGGTGAGCCC A G SGSM2 Ensembl:ENSG00000141258 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2361612..2361831 26863196 MeRIP-seq:(Medium) rs1200801852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899067,Human_RBP_ID_9375070,Human_RBP_ID_18987547 Human_Splice_Rec_1759747,Human_Splice_Rec_1759753,Human_Splice_Rec_1759799,Human_Splice_Rec_1759815,Human_Splice_Rec_1759859,Human_Splice_Rec_1759899 RMVar_hsa_circ_13788,RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235 103913 RMVar_ID_103913 Human_SNP_ID_614981252 m1A Human chr17 + 2362202 2362202 2362202 CCGGCCCTCAGCCCTCAGGCCTTGAAACACGTATGGGTACGCACGGCGCTCATCGAGAAAGTTCT CCGGCCCTCAGCCCTCAGGCCTTGAAACACGTTTGGGTACGCACGGCGCTCATCGAGAAAGTTCT A T SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2362064..2362205 26863196 MeRIP-seq:(Medium) rs373998365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4412069 Human_Splice_Rec_1759748,Human_Splice_Rec_1759754,Human_Splice_Rec_1759755,Human_Splice_Rec_1759800,Human_Splice_Rec_1759801,Human_Splice_Rec_1759816,Human_Splice_Rec_1759817,Human_Splice_Rec_1759860,Human_Splice_Rec_1759861,Human_Splice_Rec_1759900,Human_Splice_Rec_1759901 RMVar_hsa_circ_13788,RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235 103914 RMVar_ID_103914 Human_SNP_ID_614981948 m1A Human chr17 - 2364092 2364087 2364093 CAGAGTCAGGCTCTCTGCAGACTGGTGCAGGGAGAGGTAGCCAGGGACCGCCTCCATATCCTCCT CAGAGTCAGGCTCTCTGCAGACTGGTGCAGG______TAGCCAGGGACCGCCTCCATATCCTCCT ACCTCTC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2364059..2364210 32194978 MeRIP-seq:(Medium) rs756068914 Functional Loss DEL dbSNP153 32..37 33 - - - 103915 RMVar_ID_103915 Human_SNP_ID_614982355 m1A Human chr17 + 2365264 2365264 2365264 GCTACGGAAACGAAGCAGCATTCGCTCCGTGGATATGGAGGAGATGGGCACGGGGCGGGCCACCG GCTACGGAAACGAAGCAGCATTCGCTCCGTGGGTATGGAGGAGATGGGCACGGGGCGGGCCACCG A G SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2364906..2365314 32194978 MeRIP-seq:(Medium) rs776465047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9377272,Human_RBP_ID_23118837 Human_Splice_Rec_1759768,Human_Splice_Rec_1759769,Human_Splice_Rec_1759830,Human_Splice_Rec_1759831,Human_Splice_Rec_1759874,Human_Splice_Rec_1759875,Human_Splice_Rec_1759910,Human_Splice_Rec_1759911 RMVar_hsa_circ_13788,RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_181238 103916 RMVar_ID_103916 Human_SNP_ID_614984637 m1A Human chr17 + 2372469 2372469 2372469 CTCCGCGGGCCTCACCAAGGACGTGTGGAGCAAGTATCAGAAGGACAAAAAGGTGCCAACCCTGG CTCCGCGGGCCTCACCAAGGACGTGTGGAGCATGTATCAGAAGGACAAAAAGGTGCCAACCCTGG A T SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:2372348..2372474 26863196 MeRIP-seq:(Medium) rs752649327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820373 Human_Splice_Rec_1759777,Human_Splice_Rec_1759837,Human_Splice_Rec_1759881 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103917 RMVar_ID_103917 Human_SNP_ID_614984652 m1A Human chr17 + 2372514 2372514 2372514 CAAAAAGGTGCCAACCCTGGGGTTCCAGGGCCACAGGTCGAGGGGCTGGGGCGGGCAGGAGTGAG CAAAAAGGTGCCAACCCTGGGGTTCCAGGGCCGCAGGTCGAGGGGCTGGGGCGGGCAGGAGTGAG A G SGSM2 Ensembl:ENSG00000141258 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:2372512..2372600;chr17:2372509..2372705 26863196 MeRIP-seq:(Medium) rs889313481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897221,Human_RBP_ID_19077933,Human_RBP_ID_25257978 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103918 RMVar_ID_103918 Human_SNP_ID_614984794 m1A Human chr17 + 2372893 2372893 2372893 CGCCCCAGCCCATTCTCCGTGGGATGGGGCTCACCCAGCTGGGCCACGGTGACTGTGGAGGCTGC CGCCCCAGCCCATTCTCCGTGGGATGGGGCTCGCCCAGCTGGGCCACGGTGACTGTGGAGGCTGC A G SGSM2 Ensembl:ENSG00000141258 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2372889..2373089 32194978 MeRIP-seq:(Medium) rs1486569962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22544127,Human_RBP_ID_22659771 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103919 RMVar_ID_103919 Human_SNP_ID_614984893 m1A Human chr17 + 2373067 2373067 2373067 TGCTTGGCCACTACAAGTTCGGCATGAGCAAGAAGGAGATGGAGCAGGTGAGGGGAGCCTGTTCC TGCTTGGCCACTACAAGTTCGGCATGAGCAAGGAGGAGATGGAGCAGGTGAGGGGAGCCTGTTCC A G SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2373017..2373110 26863196 MeRIP-seq:(Medium) rs200527159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9375076,Human_RBP_ID_18989952 Human_Splice_Rec_1759779,Human_Splice_Rec_1759839,Human_Splice_Rec_1759883,Human_Splice_Rec_1759917 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_50152,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103920 RMVar_ID_103920 Human_SNP_ID_614984902 m1A Human chr17 + 2373080 2373080 2373080 CAAGTTCGGCATGAGCAAGAAGGAGATGGAGCAGGTGAGGGGAGCCTGTTCCCATGGGGCTGATG CAAGTTCGGCATGAGCAAGAAGGAGATGGAGCGGGTGAGGGGAGCCTGTTCCCATGGGGCTGATG A G SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2372951..2373114 26863196 MeRIP-seq:(Medium) rs774146142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9375076,Human_RBP_ID_18989952 Human_Splice_Rec_1759779,Human_Splice_Rec_1759839,Human_Splice_Rec_1759883,Human_Splice_Rec_1759917 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_50152,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103921 RMVar_ID_103921 Human_SNP_ID_614985041 m1A Human chr17 + 2373380 2373380 2373380 AGCAAGGTACCAGCAGGTGTTGGCAGAGTGGAAGGCCTGCGAGGTGGTGGTGAGGCAGCGGGAGC AGCAAGGTACCAGCAGGTGTTGGCAGAGTGGAGGGCCTGCGAGGTGGTGGTGAGGCAGCGGGAGC A G SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:2373302..2373497;chr17:2373288..2373468;chr17:2373292..2373463 26863196 MeRIP-seq:(Medium) rs1417402573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822201,Human_RBP_ID_3951618,Human_RBP_ID_5525203,Human_RBP_ID_9375077,Human_RBP_ID_18987564,Human_RBP_ID_19077935,Human_RBP_ID_26331030,Human_RBP_ID_27813289 Human_Splice_Rec_1759780,Human_Splice_Rec_1759840,Human_Splice_Rec_1759884,Human_Splice_Rec_1759918 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_50152,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 103922 RMVar_ID_103922 Human_SNP_ID_614990235 m1A Human chr17 - 2387966 2387966 2387966 CGTGAGAAGATTGCCACGCAGCAGCGGCTGGCAGAGCTCAAGCACGAGCTGAGCCAGTGGATGGA CGTGAGAAGATTGCCACGCAGCAGCGGCTGGCCGAGCTCAAGCACGAGCTGAGCCAGTGGATGGA T G MNT Ensembl:ENSG00000070444 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2387916..2388082 26863196 MeRIP-seq:(Medium) rs770413123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1759946,Human_Splice_Rec_1759950,Human_Splice_Rec_1759954,Human_Splice_Rec_1759960,Human_Splice_Rec_1759966 103923 RMVar_ID_103923 Human_SNP_ID_614990467 m1A Human chr17 + 2388769 2388769 2388769 GGCTGTTGCGTCCCATGACCCAGCTCCCCTCCACACTCAGTCTTTCCCGTGCTCCAACCCGACAC GGCTGTTGCGTCCCATGACCCAGCTCCCCTCCTCACTCAGTCTTTCCCGTGCTCCAACCCGACAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2388759..2389098 26863196 MeRIP-seq:(Medium) rs996437869 Functional Loss SNV dbSNP153 33..33 33 - - - 103924 RMVar_ID_103924 Human_SNP_ID_614990558 m1A Human chr17 - 2389036 2389034 2389036 CTGTGTGTGATGAGGGCAGACGGGGTTCAGAGAGGAAAACCAAGGCGGGCTGGTGAGTTGTGTGT CTGTGTGTGATGAGGGCAGACGGGGTTCAGAG__GAAAACCAAGGCGGGCTGGTGAGTTGTGTGT CCT C MNT Ensembl:ENSG00000070444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:2388250..2389237;chr17:2388056..2389323 26863196 MeRIP-seq:(Medium) rs1365832213 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_820057,Human_RBP_ID_2497559,Human_RBP_ID_8092491 103925 RMVar_ID_103925 Human_SNP_ID_614990559 m1A Human chr17 - 2389036 2389036 2389036 CTGTGTGTGATGAGGGCAGACGGGGTTCAGAGAGGAAAACCAAGGCGGGCTGGTGAGTTGTGTGT CTGTGTGTGATGAGGGCAGACGGGGTTCAGAGTGGAAAACCAAGGCGGGCTGGTGAGTTGTGTGT T A MNT Ensembl:ENSG00000070444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:2388250..2389237;chr17:2388056..2389323 26863196 MeRIP-seq:(Medium) rs1295652116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820057,Human_RBP_ID_2497559,Human_RBP_ID_8092491 103926 RMVar_ID_103926 Human_SNP_ID_614991757 m1A Human chr17 + 2392759 2392757 2392759 CCCTCGCCGGCTGCACCGCCCTCCGCGACTCGAGAGCACCGCCCCCGCCCGCTGCAGCCAATCCG CCCTCGCCGGCTGCACCGCCCTCCGCGACTC__GAGCACCGCCCCCGCCCGCTGCAGCCAATCCG CGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2392473..2392801 26863196 MeRIP-seq:(Medium) rs1410179274 Functional Loss DEL dbSNP153 32..33 33 - - - 103927 RMVar_ID_103927 Human_SNP_ID_614991759 m1A Human chr17 + 2392759 2392759 2392759 CCCTCGCCGGCTGCACCGCCCTCCGCGACTCGAGAGCACCGCCCCCGCCCGCTGCAGCCAATCCG CCCTCGCCGGCTGCACCGCCCTCCGCGACTCGTGAGCACCGCCCCCGCCCGCTGCAGCCAATCCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2392473..2392801 26863196 MeRIP-seq:(Medium) rs1477860627 Functional Loss SNV dbSNP153 33..33 33 - - - 103928 RMVar_ID_103928 Human_SNP_ID_614992154 m1A Human chr17 + 2393364 2393364 2393364 GAGGGAGCGACGCCCAAAGGGAGGGGACGCGCAGCCGGGAGGGCCCCGAAAAAAGAGACACCCCC GAGGGAGCGACGCCCAAAGGGAGGGGACGCGCTGCCGGGAGGGCCCCGAAAAAAGAGACACCCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2393359..2393479 26863196 MeRIP-seq:(Medium) rs1402566414 Functional Loss SNV dbSNP153 33..33 33 - - - 103929 RMVar_ID_103929 Human_SNP_ID_614993342 m1A Human chr17 - 2395378 2395378 2395378 CAGAAGAAGGCCAATAGCCTGGCCAGGCTGGCACATACCCTTCCTGTGGAGGAACCCCGCATGGA CAGAAGAAGGCCAATAGCCTGGCCAGGCTGGCGCATACCCTTCCTGTGGAGGAACCCCGCATGGA T C MNT Ensembl:ENSG00000070444 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2395328..2395438 32194978 MeRIP-seq:(Medium) rs895646667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5365940 Human_Splice_Rec_1759940,Human_Splice_Rec_1759968 RMVar_hsa_circ_282827,RMVar_hsa_circ_87021,RMVar_hsa_circ_181245,RMVar_hsa_circ_181244 103930 RMVar_ID_103930 Human_SNP_ID_614994872 m1A Human chr17 - 2400159 2400157 2400159 GTATAGCACACGAGTGGGCGTGTGTGTAACGGAGTGGGGGTGGGGACTACTCTACGCGGAGCAGC GTATAGCACACGAGTGGGCGTGTGTGTAACGG__TGGGGGTGGGGACTACTCTACGCGGAGCAGC ACT A MNT Ensembl:ENSG00000070444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2400157..2400309 26863196 MeRIP-seq:(Medium) rs1383150236 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18459503,Human_RBP_ID_24372083 RMVar_hsa_circ_87021,RMVar_hsa_circ_181244 103931 RMVar_ID_103931 Human_SNP_ID_614994875 m1A Human chr17 + 2400167 2400164 2400168 GCGTAGAGTAGTCCCCACCCCCACTCCGTTACACACACGCCCACTCGTGTGCTATACACACGCCC GCGTAGAGTAGTCCCCACCCCCACTCCGTT____ACACGCCCACTCGTGTGCTATACACACGCCC TACAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2400165..2400318 26863196 MeRIP-seq:(Medium) rs992657312 Functional Loss DEL dbSNP153 31..34 33 - - - 103932 RMVar_ID_103932 Human_SNP_ID_614995010 m1A Human chr17 + 2400625 2400625 2400625 TCGCTTCCCCTTCCCCAGTGCCCCAGGGGCCCAGCCCGGCCGCTCACCACGTGCTCTCTGTTGTT TCGCTTCCCCTTCCCCAGTGCCCCAGGGGCCCCGCCCGGCCGCTCACCACGTGCTCTCTGTTGTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2400619..2401120 26863196 MeRIP-seq:(Medium) rs754502192 Functional Loss SNV dbSNP153 33..33 33 - - - 103933 RMVar_ID_103933 Human_SNP_ID_615001205 m1A Human chr17 - 2418676 2418676 2418676 GATCAGGCCCTCGGCAGAGACACAGGAAGCGGAACTGCTGTGCCTTAACTTGGCTGTGGAGCTGG GATCAGGCCCTCGGCAGAGACACAGGAAGCGGTACTGCTGTGCCTTAACTTGGCTGTGGAGCTGG T A METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2418628..2418696 26863196 MeRIP-seq:(Medium) rs1184870477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6570640,Human_RBP_ID_12930909 RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 103934 RMVar_ID_103934 Human_SNP_ID_615001670 m1A Human chr17 + 2420328 2420328 2420328 ACAGGGACTCCTGGCTCGGGCACGGGCCCTCCACAGCGGCAGCCTCGCCTTCCCGCAGAGCAGGC ACAGGGACTCCTGGCTCGGGCACGGGCCCTCCGCAGCGGCAGCCTCGCCTTCCCGCAGAGCAGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2420278..2420355 26863196 MeRIP-seq:(Medium) rs746541128 Functional Loss SNV dbSNP153 33..33 33 - - - 103935 RMVar_ID_103935 Human_SNP_ID_615001700 m1A Human chr17 - 2420379 2420379 2420379 TGGCAATAGCCAAGAACTGGCCAGGGGCCCCCAGGAGAGGACCCCCTGTGGGCCTGCTCTGCGGG TGGCAATAGCCAAGAACTGGCCAGGGGCCCCCGGGAGAGGACCCCCTGTGGGCCTGCTCTGCGGG T C METTL16 Ensembl:ENSG00000127804 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2420335..2420435 32194978 MeRIP-seq:(Medium) rs1393217605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5525218 Human_miRNA_ID_2041016,Human_miRNA_ID_3020000,Human_miRNA_ID_3044941 RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 103936 RMVar_ID_103936 Human_SNP_ID_615025292 m1A Human chr17 - 2506124 2506124 2506124 CTAAGAATTTGCCGACTGAAGAGAGGGAGGAAAAAACGTTACAGATAAAAAGAATAACCTGCATA CTAAGAATTTGCCGACTGAAGAGAGGGAGGAAGAAACGTTACAGATAAAAAGAATAACCTGCATA T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2506122..2506220 26863196 MeRIP-seq:(Medium) rs189512379 Functional Loss SNV dbSNP153 33..33 33 - - - 103937 RMVar_ID_103937 Human_SNP_ID_615026305 m1A Human chr17 - 2508888 2508885 2508888 ACAGACTACCATGCAGCAGAGAAAATGGAAGAAGACCAGTATGTCTGGAAGGGGAAAGTGGCAAC ACAGACTACCATGCAGCAGAGAAAATGGAAGA___CCAGTATGTCTGGAAGGGGAAAGTGGCAAC GTCT G METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2508875..2509038 26863196 MeRIP-seq:(Medium) rs1324683947 Functional Loss DEL dbSNP153 33..35 33 - - - 103938 RMVar_ID_103938 Human_SNP_ID_615026966 m1A Human chr17 - 2511453 2511453 2511453 AAACTGAGCTGATAAAATGAGGGCATGGAAAGAACGGCAGTGGCAGGACTAGTGGGAAACGTCGG AAACTGAGCTGATAAAATGAGGGCATGGAAAGCACGGCAGTGGCAGGACTAGTGGGAAACGTCGG T G METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2511256..2511758 26863196 MeRIP-seq:(Medium) rs1436069940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12932003,Human_RBP_ID_23716658 103939 RMVar_ID_103939 Human_SNP_ID_615027067 m1A Human chr17 - 2511835 2511835 2511835 AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTATGCGGCTGCTTTAAGATTCTAGGGTTGTACAG AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTTTGCGGCTGCTTTAAGATTCTAGGGTTGTACAG T A METTL16 Ensembl:ENSG00000127804 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:2511738..2511836;chr17:2511758..2511871 26863196 MeRIP-seq:(Medium) rs557674881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4412309,Human_RBP_ID_9377284,Human_RBP_ID_18691869 Human_Splice_Rec_1759981,Human_Splice_Rec_1759999,Human_Splice_Rec_1760015,Human_Splice_Rec_1760029,Human_Splice_Rec_1760055 103940 RMVar_ID_103940 Human_SNP_ID_615027068 m1A Human chr17 - 2511835 2511835 2511835 AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTATGCGGCTGCTTTAAGATTCTAGGGTTGTACAG AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTGTGCGGCTGCTTTAAGATTCTAGGGTTGTACAG T C METTL16 Ensembl:ENSG00000127804 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:2511738..2511836;chr17:2511758..2511871 26863196 MeRIP-seq:(Medium) rs557674881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4412309,Human_RBP_ID_9377284,Human_RBP_ID_18691869 Human_Splice_Rec_1759981,Human_Splice_Rec_1759999,Human_Splice_Rec_1760015,Human_Splice_Rec_1760029,Human_Splice_Rec_1760055 103941 RMVar_ID_103941 Human_SNP_ID_615027069 m1A Human chr17 - 2511835 2511835 2511835 AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTATGCGGCTGCTTTAAGATTCTAGGGTTGTACAG AGCGTATCATCTGCGTTTCTAGGAGCTTCGCTCTGCGGCTGCTTTAAGATTCTAGGGTTGTACAG T G METTL16 Ensembl:ENSG00000127804 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:2511738..2511836;chr17:2511758..2511871 26863196 MeRIP-seq:(Medium) rs557674881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4412309,Human_RBP_ID_9377284,Human_RBP_ID_18691869 Human_Splice_Rec_1759981,Human_Splice_Rec_1759999,Human_Splice_Rec_1760015,Human_Splice_Rec_1760029,Human_Splice_Rec_1760055 103942 RMVar_ID_103942 Human_SNP_ID_615057090 m1A Human chr17 + 2615884 2615884 2615884 GCAATAAGGATGCACCCAGGAGGTGATAAGGAAATCCAGGAGGTGATAAGGTAGACAGACTGAGA GCAATAAGGATGCACCCAGGAGGTGATAAGGAGATCCAGGAGGTGATAAGGTAGACAGACTGAGA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2615870..2615965 26863196 MeRIP-seq:(Medium) rs1363977866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8447094,Human_RBP_ID_12932883 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_323378 103943 RMVar_ID_103943 Human_SNP_ID_615075734 m1A Human chr17 + 2681705 2681701 2681705 GTTTGTTGTCCAGGCTTACGTGTGAGTTTTAAATAAACCATTTCTTTTTCTTTCAGATTTCCACA GTTTGTTGTCCAGGCTTACGTGTGAGTTT____TAAACCATTTCTTTTTCTTTCAGATTTCCACA TTAAA T PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2681699..2681831 26863196 MeRIP-seq:(Medium) rs555399151 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_6571689,Human_RBP_ID_8093629,Human_RBP_ID_9070017,Human_RBP_ID_17489633,Human_RBP_ID_22803583,Human_RBP_ID_23275278,Human_RBP_ID_23717177,Human_RBP_ID_25259141,Human_RBP_ID_27662666 RMVar_hsa_circ_87407,RMVar_hsa_circ_181272 103944 RMVar_ID_103944 Human_SNP_ID_615075736 m1A Human chr17 + 2681705 2681705 2681705 GTTTGTTGTCCAGGCTTACGTGTGAGTTTTAAATAAACCATTTCTTTTTCTTTCAGATTTCCACA GTTTGTTGTCCAGGCTTACGTGTGAGTTTTAATTAAACCATTTCTTTTTCTTTCAGATTTCCACA A T PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2681699..2681831 26863196 MeRIP-seq:(Medium) rs752955476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6571689,Human_RBP_ID_8093629,Human_RBP_ID_9070017,Human_RBP_ID_17489633,Human_RBP_ID_22803583,Human_RBP_ID_23275278,Human_RBP_ID_23717177,Human_RBP_ID_25259141,Human_RBP_ID_27662666 RMVar_hsa_circ_87407,RMVar_hsa_circ_181272 103945 RMVar_ID_103945 Human_SNP_ID_615078411 m1A Human chr17 - 2689775 2689775 2689775 GGCCGGGGGCGAGGCTGGGGGAAGCGGGGCCCAATTACGGATCCCGGGAGTTACAGGTGCCGACG GGCCGGGGGCGAGGCTGGGGGAAGCGGGGCCCGATTACGGATCCCGGGAGTTACAGGTGCCGACG T C CLUH Ensembl:ENSG00000132361 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2689727..2689924 26863196 MeRIP-seq:(Medium) rs1448788347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189200,Human_RBP_ID_8253248,Human_RBP_ID_9288672,Human_RBP_ID_17887581,Human_RBP_ID_18459505,Human_RBP_ID_26448232 Human_miRNA_ID_2296033 RMVar_hsa_circ_97722,RMVar_hsa_circ_181278 103946 RMVar_ID_103946 Human_SNP_ID_615078515 m1A Human chr17 + 2690027 2690027 2690027 ACAACGGCGGCTCCCGTCCCGCCCCAAACTAAAGTGCACCCCAGCCCTCCAGCCCCGCCACAGAG ACAACGGCGGCTCCCGTCCCGCCCCAAACTAAGGTGCACCCCAGCCCTCCAGCCCCGCCACAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2689976..2690189 26863196 MeRIP-seq:(Medium) rs924313641 Functional Loss SNV dbSNP153 33..33 33 - - - 103947 RMVar_ID_103947 Human_SNP_ID_615078721 m1A Human chr17 - 2690484 2690484 2690484 GGGCGGAAGAGGAAGCAAGGCCCTCTTCCTCCACGTCTCACCCCACCCCACCCCCGTGTCCTCCT GGGCGGAAGAGGAAGCAAGGCCCTCTTCCTCCGCGTCTCACCCCACCCCACCCCCGTGTCCTCCT T C CLUH Ensembl:ENSG00000132361 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2690435..2690647 26863196 MeRIP-seq:(Medium) rs758420086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301084 Human_miRNA_ID_3078543 RMVar_hsa_circ_97722,RMVar_hsa_circ_181278 103948 RMVar_ID_103948 Human_SNP_ID_615079935 m1A Human chr17 + 2692075 2692075 2692075 CAGGGCCGACCGGAACTCAGCTTTGCTCTCGTAGACTCGGGCGACAAGGTGGTGGCTGCCGGGAG CAGGGCCGACCGGAACTCAGCTTTGCTCTCGTGGACTCGGGCGACAAGGTGGTGGCTGCCGGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2692026..2692075 32194978 MeRIP-seq:(Medium) rs748480811 Functional Loss SNV dbSNP153 33..33 33 - - - 103949 RMVar_ID_103949 Human_SNP_ID_615081003 m1A Human chr17 - 2694251 2694251 2694251 CCCCCAGGTCCTGCTGAAGGAGTACAGCTTCGACAGTCGCCACAAGCCCGCGTTCACCGAGGAGG CCCCCAGGTCCTGCTGAAGGAGTACAGCTTCGGCAGTCGCCACAAGCCCGCGTTCACCGAGGAGG T C CLUH Ensembl:ENSG00000132361 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2694201..2695011 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4412694,Human_RBP_ID_19077953,Human_RBP_ID_26957303 Human_Splice_Rec_1760198,Human_Splice_Rec_1760244,Human_Splice_Rec_1760292,Human_Splice_Rec_1760340,Human_Splice_Rec_1760386,Human_Splice_Rec_1760406 RMVar_hsa_circ_97722,RMVar_hsa_circ_181278,RMVar_hsa_circ_375860,RMVar_hsa_circ_76172,RMVar_hsa_circ_181279,RMVar_hsa_circ_111665,RMVar_hsa_circ_181281,RMVar_hsa_circ_181282 103950 RMVar_ID_103950 Human_SNP_ID_615082247 m1A Human chr17 - 2696703 2696703 2696703 CGCAGACGACGGCACAGGTGGGGCTGCTGCAGATGGCCGGGAGAGAGCCCGGGCTGGCCCTGCCA CGCAGACGACGGCACAGGTGGGGCTGCTGCAGGTGGCCGGGAGAGAGCCCGGGCTGGCCCTGCCA T C CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2696701..2696825 26863196 MeRIP-seq:(Medium) rs1192827597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17887607,Human_RBP_ID_19080983 RMVar_hsa_circ_50832,RMVar_hsa_circ_111665,RMVar_hsa_circ_181282 103951 RMVar_ID_103951 Human_SNP_ID_615082277 m1A Human chr17 + 2696769 2696769 2696769 CGATGGTCTCTGCCAGCTCCTTCACCTTGGCCAGGCCGCTGGCGCTGCTACCCTCCTCCTCACTT CGATGGTCTCTGCCAGCTCCTTCACCTTGGCCTGGCCGCTGGCGCTGCTACCCTCCTCCTCACTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2696701..2696825 26863196 MeRIP-seq:(Medium) rs1248458854 Functional Loss SNV dbSNP153 33..33 33 - - - 103952 RMVar_ID_103952 Human_SNP_ID_615082840 m1A Human chr17 + 2698022 2698020 2698023 GCAGCTCCTCGCCAGGCACGGGCAGGAAGTTGAGGTCCGGGGGGAAGGTGCGCAGCAGGTCGAGG GCAGCTCCTCGCCAGGCACGGGCAGGAAGTT___GTCCGGGGGGAAGGTGCGCAGCAGGTCGAGG TGAG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2697971..2698112 26863196 MeRIP-seq:(Medium) rs1309651163 Functional Loss DEL dbSNP153 32..34 33 - - - 103953 RMVar_ID_103953 Human_SNP_ID_615082947 m1A Human chr17 + 2698206 2698206 2698206 GCGCTCCAGCAGCTCCAGGTACCGCGGGTGTGACACCACGGTCTTGCCGAAGTCGATGGAGCCGT GCGCTCCAGCAGCTCCAGGTACCGCGGGTGTGCCACCACGGTCTTGCCGAAGTCGATGGAGCCGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2696207..2698215 32194978 MeRIP-seq:(Medium) rs1182046214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181287 103954 RMVar_ID_103954 Human_SNP_ID_615085346 m1A Human chr17 - 2704702 2704702 2704702 TGTGGAAGTGGCCTGCAGGTGCACGGAGGGCGAGGCGCGACCGTGAGGCTGGGACTCTCGAGGGC TGTGGAAGTGGCCTGCAGGTGCACGGAGGGCGGGGCGCGACCGTGAGGCTGGGACTCTCGAGGGC T C CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2704696..2705255 26863196 MeRIP-seq:(Medium) rs986143541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50600,Human_RBP_ID_3542474,Human_RBP_ID_8091849,Human_RBP_ID_8189202,Human_RBP_ID_9423838,Human_RBP_ID_18486283,Human_RBP_ID_22715652,Human_RBP_ID_22740810 103955 RMVar_ID_103955 Human_SNP_ID_615085390 m1A Human chr17 - 2704813 2704813 2704813 TGGCTTGAAGGGTGGCTTTGGTGACCCTGGGGAGAGTGGTTTGGGACATGGGTTCAGGTGCAAGC TGGCTTGAAGGGTGGCTTTGGTGACCCTGGGGGGAGTGGTTTGGGACATGGGTTCAGGTGCAAGC T C CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2704810..2705035 26863196 MeRIP-seq:(Medium) rs534807908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18941179 103956 RMVar_ID_103956 Human_SNP_ID_615085584 m1A Human chr17 - 2705636 2705636 2705636 TGCAGCCGAATGTCTCTGGGAATGAAAGGGGGAGGGAGTGTGATTCTGCCATTAAGGGTCATTTG TGCAGCCGAATGTCTCTGGGAATGAAAGGGGGGGGGAGTGTGATTCTGCCATTAAGGGTCATTTG T C CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2705634..2705700 26863196 MeRIP-seq:(Medium) rs1392555455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5318825 103957 RMVar_ID_103957 Human_SNP_ID_615085966 m1A Human chr17 - 2707043 2707043 2707043 AGGATTAGGGTAAAACATGCTGTCCTGGGGAGAGGAGGCCCCTTGGGAGCCAGCTGCATTCCTTT AGGATTAGGGTAAAACATGCTGTCCTGGGGAGCGGAGGCCCCTTGGGAGCCAGCTGCATTCCTTT T G CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2707035..2707131 26863196 MeRIP-seq:(Medium) rs147481752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8091853 103958 RMVar_ID_103958 Human_SNP_ID_615086383 m1A Human chr17 - 2708536 2708536 2708536 GGTTGGCTCCTCTTGCCTCTGTGACCTTGGGCAGCTGCTTCCTAGCCTTCTGGAGCCTCAGTTTC GGTTGGCTCCTCTTGCCTCTGTGACCTTGGGCGGCTGCTTCCTAGCCTTCTGGAGCCTCAGTTTC T C CLUH Ensembl:ENSG00000132361 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:2708533..2708915 26863196 MeRIP-seq:(Medium) rs1222633297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12935549,Human_RBP_ID_22948129 103959 RMVar_ID_103959 Human_SNP_ID_615087403 m1A Human chr17 - 2711679 2711679 2711679 GGCGCGGCGGGCGGCGCGGACAGCCGAGGCGGACGCCCGCTCCCGCCACCATGGTTATCAAGACG GGCGCGGCGGGCGGCGCGGACAGCCGAGGCGGTCGCCCGCTCCCGCCACCATGGTTATCAAGACG T A CLUH Ensembl:ENSG00000132361 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:2711616..2711759 26863196 MeRIP-seq:(Medium) rs1283975617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6660,Human_RBP_ID_4464231,Human_RBP_ID_18163869,Human_RBP_ID_18419825,Human_RBP_ID_27838360 103960 RMVar_ID_103960 Human_SNP_ID_615143345 m1A Human chr17 + 2905325 2905325 2905325 GCTGGCCAACAGCTCGGATGCGACCCTCCCAGACCGGCCGCTCTCCCCTCCTCTCACGGCACCTC GCTGGCCAACAGCTCGGATGCGACCCTCCCAGGCCGGCCGCTCTCCCCTCCTCTCACGGCACCTC A G RAP1GAP2 Ensembl:ENSG00000132359 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2905270..2905405 26863196 MeRIP-seq:(Medium) rs749102479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1760472,Human_Splice_Rec_1760473,Human_Splice_Rec_1760520,Human_Splice_Rec_1760521,Human_Splice_Rec_1760568,Human_Splice_Rec_1760569,Human_Splice_Rec_1760614,Human_Splice_Rec_1760615,Human_Splice_Rec_1760662,Human_Splice_Rec_1760663 RMVar_hsa_circ_181293,RMVar_hsa_circ_125490 103961 RMVar_ID_103961 Human_SNP_ID_615160194 m1A Human chr17 - 2963965 2963965 2963965 GGCTGAGGTTGTCCTCTTCCTCCTCCTCACAGATGCTGCTCCCCAGCGATGTTGGGGTGCCCACG GGCTGAGGTTGTCCTCTTCCTCCTCCTCACAGGTGCTGCTCCCCAGCGATGTTGGGGTGCCCACG T C AC015921.1 Ensembl:ENSG00000262884 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2963916..2963994 26863196 MeRIP-seq:(Medium) rs1157229211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1760726,Human_Splice_Rec_1760727 103962 RMVar_ID_103962 Human_SNP_ID_615169632 m1A Human chr17 + 2998870 2998870 2998870 GATGCCATTTGCTCGAGTAAGGCAGAGCTGGAATAAAGAAAGAGCGTGGAAAGGACGAGCAGGAA GATGCCATTTGCTCGAGTAAGGCAGAGCTGGAGTAAAGAAAGAGCGTGGAAAGGACGAGCAGGAA A G RAP1GAP2 Ensembl:ENSG00000132359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2998857..2998963 26863196 MeRIP-seq:(Medium) rs934529618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26641091 RMVar_hsa_circ_87934,RMVar_hsa_circ_336452,RMVar_hsa_circ_75381,RMVar_hsa_circ_181295,RMVar_hsa_circ_49514,RMVar_hsa_circ_340293 103963 RMVar_ID_103963 Human_SNP_ID_615342396 m1A Human chr17 - 3627154 3627154 3627154 GACAAAGGACAGGTCAGCACGTGTAAAGAACCAGTAACTAAGAGAGAACAAGCAGCTCTGTGGAA GACAAAGGACAGGTCAGCACGTGTAAAGAACCCGTAACTAAGAGAGAACAAGCAGCTCTGTGGAA T G AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3627152..3627220 26863196 MeRIP-seq:(Medium) rs541069127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12979406 RMVar_hsa_circ_82198,RMVar_hsa_circ_181317,RMVar_hsa_circ_181319,RMVar_hsa_circ_109633,RMVar_hsa_circ_314618,RMVar_hsa_circ_181318 103964 RMVar_ID_103964 Human_SNP_ID_615345210 m1A Human chr17 - 3636188 3636188 3636188 AATGGCTGCGCGGCCGATCACCCTCGGCATTGACCTGGGCACCACATCTGTGAAGGCAGCTCTGC AATGGCTGCGCGGCCGATCACCCTCGGCATTGGCCTGGGCACCACATCTGTGAAGGCAGCTCTGC T C AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3636123..3636206 26863196 MeRIP-seq:(Medium) rs1466392894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465058,Human_RBP_ID_5496903,Human_RBP_ID_18695632 Human_miRNA_ID_707898,Human_miRNA_ID_707899,Human_miRNA_ID_715158,Human_miRNA_ID_715159,Human_miRNA_ID_1516945,Human_miRNA_ID_1516946 RMVar_hsa_circ_109633,RMVar_hsa_circ_181318 103965 RMVar_ID_103965 Human_SNP_ID_615345211 m1A Human chr17 - 3636188 3636188 3636188 AATGGCTGCGCGGCCGATCACCCTCGGCATTGACCTGGGCACCACATCTGTGAAGGCAGCTCTGC AATGGCTGCGCGGCCGATCACCCTCGGCATTGCCCTGGGCACCACATCTGTGAAGGCAGCTCTGC T G AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3636123..3636206 26863196 MeRIP-seq:(Medium) rs1466392894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465058,Human_RBP_ID_5496903,Human_RBP_ID_18695632 Human_miRNA_ID_707898,Human_miRNA_ID_707899,Human_miRNA_ID_715158,Human_miRNA_ID_715159,Human_miRNA_ID_1516945,Human_miRNA_ID_1516946 RMVar_hsa_circ_109633,RMVar_hsa_circ_181318 103966 RMVar_ID_103966 Human_SNP_ID_615345567 m1A Human chr17 - 3637170 3637170 3637170 AGGATGGGGTCTCGTGCTGCTCAGTCCCCCGGAGCCCCGCACTCCGCACGTCAACCGGCGCTCTC AGGATGGGGTCTCGTGCTGCTCAGTCCCCCGGGGCCCCGCACTCCGCACGTCAACCGGCGCTCTC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:3637143..3637269 26863196 MeRIP-seq:(Medium) rs897729691 Functional Loss SNV dbSNP153 33..33 33 - - - 103967 RMVar_ID_103967 Human_SNP_ID_615351025 m1A Human chr17 - 3655835 3655835 3655835 CCCTCAAGTCCTGGCTCCAGAGGGGAGTCAGGAGGCCCCCGGAAGAAAGCGTCTCCCTCCCGGCT CCCTCAAGTCCTGGCTCCAGAGGGGAGTCAGGGGGCCCCCGGAAGAAAGCGTCTCCCTCCCGGCT T C AC027796.4 Ensembl:ENSG00000262903 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3655799..3656048 26863196 MeRIP-seq:(Medium) rs1210601713 Functional Loss SNV dbSNP153 33..33 33 - - - 103968 RMVar_ID_103968 Human_SNP_ID_615351344 m1A Human chr17 - 3656482 3656482 3656482 CACGAAGTCGAAGCTCAGACCAATGACACTGCAGGGGGTGGAGGGACAAGACAGGGCAGGGGGTG CACGAAGTCGAAGCTCAGACCAATGACACTGCGGGGGGTGGAGGGACAAGACAGGGCAGGGGGTG T C AC027796.4 Ensembl:ENSG00000262903 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3656431..3656688 26863196 MeRIP-seq:(Medium) rs1407795329 Functional Loss SNV dbSNP153 33..33 33 - - - 103969 RMVar_ID_103969 Human_SNP_ID_615351345 m1A Human chr17 - 3656487 3656487 3656487 AGAGCCACGAAGTCGAAGCTCAGACCAATGACACTGCAGGGGGTGGAGGGACAAGACAGGGCAGG AGAGCCACGAAGTCGAAGCTCAGACCAATGACGCTGCAGGGGGTGGAGGGACAAGACAGGGCAGG T C AC027796.4 Ensembl:ENSG00000262903 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3656436..3656683 26863196 MeRIP-seq:(Medium) rs77453839 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5579175 Clinvar_Rec_646 103970 RMVar_ID_103970 Human_SNP_ID_615351346 m1A Human chr17 - 3656487 3656487 3656487 AGAGCCACGAAGTCGAAGCTCAGACCAATGACACTGCAGGGGGTGGAGGGACAAGACAGGGCAGG AGAGCCACGAAGTCGAAGCTCAGACCAATGACCCTGCAGGGGGTGGAGGGACAAGACAGGGCAGG T G AC027796.4 Ensembl:ENSG00000262903 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3656436..3656683 26863196 MeRIP-seq:(Medium) rs77453839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5579175 Clinvar_Rec_646 103971 RMVar_ID_103971 Human_SNP_ID_615351495 m1A Human chr17 - 3656797 3656797 3656797 GGGGTGGCCTGTGGGGGGCCAGGGCTGGTCTCACCTCATACAGGCAGCACTGCACGATGATGATC GGGGTGGCCTGTGGGGGGCCAGGGCTGGTCTCGCCTCATACAGGCAGCACTGCACGATGATGATC T C AC027796.4 Ensembl:ENSG00000262903 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3656748..3656832 26863196 MeRIP-seq:(Medium) rs1057516723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767156,Human_RBP_ID_819682,Human_RBP_ID_1546930,Human_RBP_ID_3544904,Human_RBP_ID_8189226,Human_RBP_ID_18941198,Human_RBP_ID_21974064 Clinvar_Rec_647 103972 RMVar_ID_103972 Human_SNP_ID_615351741 m1A Human chr17 + 3657653 3657653 3657653 CAGTACCTGGCTGGGAGAGGCACCAGGCCACCAGAGTTCCGACCCCACGTCTCCAAGTGAGTGCT CAGTACCTGGCTGGGAGAGGCACCAGGCCACCGGAGTTCCGACCCCACGTCTCCAAGTGAGTGCT A G CTNS Ensembl:ENSG00000040531 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3657637..3657703 26863196 MeRIP-seq:(Medium) rs1429133047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28248 103973 RMVar_ID_103973 Human_SNP_ID_615351809 m1A Human chr17 + 3657930 3657930 3657930 CCAGCCTCCGTGCCCCTCTCTAAGCCCGCCCTATCCGGGGCCGTCCTTGCTCAGCCCCGGCGTGG CCAGCCTCCGTGCCCCTCTCTAAGCCCGCCCTCTCCGGGGCCGTCCTTGCTCAGCCCCGGCGTGG A C CTNS Ensembl:ENSG00000040531 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3657879..3658072 26863196 MeRIP-seq:(Medium) rs1339877276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22657266 RMVar_hsa_circ_28248 103974 RMVar_ID_103974 Human_SNP_ID_615351981 m1A Human chr17 - 3658229 3658229 3658229 AGGAGCTGCCCCACCGGAGCAGGGCCTGGGCCATGTAGCTCTCACCTCTCCTGCCACCGGCCATG AGGAGCTGCCCCACCGGAGCAGGGCCTGGGCCGTGTAGCTCTCACCTCTCCTGCCACCGGCCATG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:3658182..3658287 32194978 MeRIP-seq:(Medium) rs1446714693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18695729 103975 RMVar_ID_103975 Human_SNP_ID_615353752 m1A Human chr17 - 3663260 3663260 3663260 GACTGGACACACATCCTGCCAGAGGCGCTACGAAGCTTTGCCCAGATGAAGCCAGGTGGGCTCCG GACTGGACACACATCCTGCCAGAGGCGCTACGCAGCTTTGCCCAGATGAAGCCAGGTGGGCTCCG T G TAX1BP3,P2RX5-TAX1BP3 Ensembl:ENSG00000213977,Ensembl:ENSG00000257950 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:3663211..3663559 32194978 MeRIP-seq:(Medium) rs1196166152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_487757,Human_RBP_ID_26458636 RMVar_hsa_circ_101574,RMVar_hsa_circ_181325 103976 RMVar_ID_103976 Human_SNP_ID_615354245 m1A Human chr17 - 3664800 3664800 3664800 CCCACTTCTCTCAACTGGCTTTTTTCTTTGCCAGCAAAGAGTTGAAATTCACAAGCTGCGTCAAG CCCACTTCTCTCAACTGGCTTTTTTCTTTGCCGGCAAAGAGTTGAAATTCACAAGCTGCGTCAAG T C TAX1BP3,P2RX5-TAX1BP3 Ensembl:ENSG00000213977,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:3664769..3669332 32194978 MeRIP-seq:(Medium) rs1365751816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 103977 RMVar_ID_103977 Human_SNP_ID_615355693 m1A Human chr17 - 3669202 3669202 3669202 GGCAATAATCCAGGACGGCGGCGTTGCCCCGCACGGCCGCCTCGCTGATGAACGGCGGCCCTTCC GGCAATAATCCAGGACGGCGGCGTTGCCCCGCCCGGCCGCCTCGCTGATGAACGGCGGCCCTTCC T G P2RX5-TAX1BP3 Ensembl:ENSG00000257950 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3669155..3669332 26863196 MeRIP-seq:(Medium) rs78045993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 103978 RMVar_ID_103978 Human_SNP_ID_615358505 m1A Human chr17 + 3679674 3679674 3679674 TGCTTCCACGCTTCGCCTCGGGTGGCTCCTGCAGCTCCTGCTGCTCCGGCATCCCCAGCAGCCCT TGCTTCCACGCTTCGCCTCGGGTGGCTCCTGCGGCTCCTGCTGCTCCGGCATCCCCAGCAGCCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:3679597..3679697 32194978 MeRIP-seq:(Medium) rs1461096858 Functional Loss SNV dbSNP153 33..33 33 - - - 103979 RMVar_ID_103979 Human_SNP_ID_615358851 m1A Human chr17 + 3680298 3680298 3680298 ACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCAT ACCCAGTGTCCTCCACCCTGCATCCTCCACCCGGTGTCCTCCACCCTGCATCCTCCACCCTGCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3680294..3680727 26863196 MeRIP-seq:(Medium) rs374033661 Functional Loss SNV dbSNP153 33..33 33 - - - 103980 RMVar_ID_103980 Human_SNP_ID_615358852 m1A Human chr17 + 3680298 3680298 3680298 ACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCAT ACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGTGTCCTCCACCCTGCATCCTCCACCCTGCAT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3680294..3680727 26863196 MeRIP-seq:(Medium) rs374033661 Functional Loss SNV dbSNP153 33..33 33 - - - 103981 RMVar_ID_103981 Human_SNP_ID_615358872 m1A Human chr17 + 3680329 3680327 3680329 CAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCAGTGTCCT CAGTGTCCTCCACCCTGCATCCTCCACCCTG__TCCTCCACCCTGCGTCCTCCACCCAGTGTCCT GCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680326..3680398 26863196 MeRIP-seq:(Medium) rs1325306310 Functional Loss DEL dbSNP153 32..33 33 - - - 103982 RMVar_ID_103982 Human_SNP_ID_615358874 m1A Human chr17 + 3680329 3680329 3680329 CAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCAGTGTCCT CAGTGTCCTCCACCCTGCATCCTCCACCCTGCCTCCTCCACCCTGCGTCCTCCACCCAGTGTCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680326..3680398 26863196 MeRIP-seq:(Medium) rs371332554 Functional Loss SNV dbSNP153 33..33 33 - - - 103983 RMVar_ID_103983 Human_SNP_ID_615358875 m1A Human chr17 + 3680329 3680329 3680329 CAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCAGTGTCCT CAGTGTCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCTGCGTCCTCCACCCAGTGTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680326..3680398 26863196 MeRIP-seq:(Medium) rs371332554 Functional Loss SNV dbSNP153 33..33 33 - - - 103984 RMVar_ID_103984 Human_SNP_ID_615358876 m1A Human chr17 + 3680329 3680329 3680329 CAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCAGTGTCCT CAGTGTCCTCCACCCTGCATCCTCCACCCTGCTTCCTCCACCCTGCGTCCTCCACCCAGTGTCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680326..3680398 26863196 MeRIP-seq:(Medium) rs371332554 Functional Loss SNV dbSNP153 33..33 33 - - - 103985 RMVar_ID_103985 Human_SNP_ID_615358951 m1A Human chr17 + 3680466 3680465 3680467 ACCCTGCATCCTCCACCCTGAGTCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGT ACCCTGCATCCTCCACCCTGAGTCCTCCACCC__TGTCCTCCACCCTGCATCCTCCACCCAGTGT CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680462..3680622 26863196 MeRIP-seq:(Medium) rs1212940814 Functional Loss DEL dbSNP153 33..34 33 - - - 103986 RMVar_ID_103986 Human_SNP_ID_615358952 m1A Human chr17 + 3680466 3680466 3680466 ACCCTGCATCCTCCACCCTGAGTCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGT ACCCTGCATCCTCCACCCTGAGTCCTCCACCCGGTGTCCTCCACCCTGCATCCTCCACCCAGTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680462..3680622 26863196 MeRIP-seq:(Medium) rs112686978 Functional Loss SNV dbSNP153 33..33 33 - - - 103987 RMVar_ID_103987 Human_SNP_ID_615358953 m1A Human chr17 + 3680466 3680466 3680466 ACCCTGCATCCTCCACCCTGAGTCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGT ACCCTGCATCCTCCACCCTGAGTCCTCCACCCTGTGTCCTCCACCCTGCATCCTCCACCCAGTGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680462..3680622 26863196 MeRIP-seq:(Medium) rs112686978 Functional Loss SNV dbSNP153 33..33 33 - - - 103988 RMVar_ID_103988 Human_SNP_ID_615359118 m1A Human chr17 + 3680793 3680779 3680793 CTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCATCCT CTGCATCCTCCACCCAGTG______________TCCTCCACCCTGCATCCTCCACCCTGCATCCT GTCCTCCACCCTGCA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680790..3680895 26863196 MeRIP-seq:(Medium) rs1185233577 Functional Loss DEL dbSNP153 20..33 33 - - - 103989 RMVar_ID_103989 Human_SNP_ID_615359121 m1A Human chr17 - 3680790 3680790 3680790 ATGCAGGGTGGAGGATGCAGGGTGGAGGATGCAGGGTGGAGGACACTGGGTGGAGGATGCAGGGT ATGCAGGGTGGAGGATGCAGGGTGGAGGATGCTGGGTGGAGGACACTGGGTGGAGGATGCAGGGT T A P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3680786..3680915 26863196 MeRIP-seq:(Medium) rs1263283931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56733,RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 103990 RMVar_ID_103990 Human_SNP_ID_615359122 m1A Human chr17 - 3680790 3680790 3680790 ATGCAGGGTGGAGGATGCAGGGTGGAGGATGCAGGGTGGAGGACACTGGGTGGAGGATGCAGGGT ATGCAGGGTGGAGGATGCAGGGTGGAGGATGCCGGGTGGAGGACACTGGGTGGAGGATGCAGGGT T G P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3680786..3680915 26863196 MeRIP-seq:(Medium) rs1263283931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56733,RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 103991 RMVar_ID_103991 Human_SNP_ID_615359125 m1A Human chr17 + 3680793 3680793 3680793 CTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCATCCT CTGCATCCTCCACCCAGTGTCCTCCACCCTGCCTCCTCCACCCTGCATCCTCCACCCTGCATCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680790..3680895 26863196 MeRIP-seq:(Medium) rs866468737 Functional Loss SNV dbSNP153 33..33 33 - - - 103992 RMVar_ID_103992 Human_SNP_ID_615359126 m1A Human chr17 + 3680793 3680793 3680793 CTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCATCCT CTGCATCCTCCACCCAGTGTCCTCCACCCTGCGTCCTCCACCCTGCATCCTCCACCCTGCATCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680790..3680895 26863196 MeRIP-seq:(Medium) rs866468737 Functional Loss SNV dbSNP153 33..33 33 - - - 103993 RMVar_ID_103993 Human_SNP_ID_615359127 m1A Human chr17 + 3680793 3680793 3680793 CTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCATCCT CTGCATCCTCCACCCAGTGTCCTCCACCCTGCTTCCTCCACCCTGCATCCTCCACCCTGCATCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680790..3680895 26863196 MeRIP-seq:(Medium) rs866468737 Functional Loss SNV dbSNP153 33..33 33 - - - 103994 RMVar_ID_103994 Human_SNP_ID_615359129 m1A Human chr17 - 3680804 3680804 3680804 ACGCTGGGTGGAGGATGCAGGGTGGAGGATGCAGGGTGGAGGATGCAGGGTGGAGGACACTGGGT ACGCTGGGTGGAGGATGCAGGGTGGAGGATGCTGGGTGGAGGATGCAGGGTGGAGGACACTGGGT T A P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3680797..3680883 26863196 MeRIP-seq:(Medium) rs1321102398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56733,RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 103995 RMVar_ID_103995 Human_SNP_ID_615363962 m1A Human chr17 - 3696025 3696025 3696025 CCCATGAGCGCACGTGGGCCGGGCGGTCCGCAAGCCCGGCTGAGAGCGCGCCATGGGGCAGGCGG CCCATGAGCGCACGTGGGCCGGGCGGTCCGCAGGCCCGGCTGAGAGCGCGCCATGGGGCAGGCGG T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:3695984..3696055 26863196 MeRIP-seq:(Medium) rs1409887190 Functional Loss SNV dbSNP153 33..33 33 - - - 103996 RMVar_ID_103996 Human_SNP_ID_615363968 m1A Human chr17 + 3696031 3696031 3696031 GCCCCATGGCGCGCTCTCAGCCGGGCTTGCGGACCGCCCGGCCCACGTGCGCTCATGGGGAGCAC GCCCCATGGCGCGCTCTCAGCCGGGCTTGCGGGCCGCCCGGCCCACGTGCGCTCATGGGGAGCAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3695981..3696267 26863196 MeRIP-seq:(Medium) rs1414534327 Functional Loss SNV dbSNP153 33..33 33 - - - 103997 RMVar_ID_103997 Human_SNP_ID_615372068 m1A Human chr17 + 3723726 3723726 3723726 CGAACTGTACGCACAAGCGCGCTCCTGACTCCAGGTGCACACCGTGGAGGCCTGAAACGAGAGCC CGAACTGTACGCACAAGCGCGCTCCTGACTCCGGGTGCACACCGTGGAGGCCTGAAACGAGAGCC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:3723701..3723788 26863410 MeRIP-seq:(Medium) rs759382807 Functional Loss SNV dbSNP153 33..33 33 - - - 103998 RMVar_ID_103998 Human_SNP_ID_615372107 m1A Human chr17 - 3723774 3723774 3723774 ACGGGACGGAAAACTGGCGGCTTGGTTTGTTCAGCGCGTCGCGGTCATGGCTCTCGTTTCAGGCC ACGGGACGGAAAACTGGCGGCTTGGTTTGTTCGGCGCGTCGCGGTCATGGCTCTCGTTTCAGGCC T C ITGAE Ensembl:ENSG00000083457 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:3723626..3723825 26863196 MeRIP-seq:(Medium) rs1413423375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1856554,Human_RBP_ID_4421951,Human_RBP_ID_8450965 Human_Splice_Rec_1761903,Human_Splice_Rec_1761961,Human_Splice_Rec_1761979,Human_Splice_Rec_1761987 RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 103999 RMVar_ID_103999 Human_SNP_ID_615372110 m1A Human chr17 + 3723777 3723777 3723777 CTGAAACGAGAGCCATGACCGCGACGCGCTGAACAAACCAAGCCGCCAGTTTTCCGTCCCGTCCC CTGAAACGAGAGCCATGACCGCGACGCGCTGAGCAAACCAAGCCGCCAGTTTTCCGTCCCGTCCC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3723658..3723825 26863196 MeRIP-seq:(Medium) rs1305303918 Functional Loss SNV dbSNP153 33..33 33 - - - 104000 RMVar_ID_104000 Human_SNP_ID_615372299 m1A Human chr17 + 3724002 3724002 3724002 TTTTCCGCACATATGGGGCTGCGGACGGCAGGAGACAGCGGCGGCCGGGCCGGGAAGCCGCGCAG TTTTCCGCACATATGGGGCTGCGGACGGCAGGCGACAGCGGCGGCCGGGCCGGGAAGCCGCGCAG A C HASPIN Ensembl:ENSG00000177602 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:3723952..3724552;chr17:3723952..3724228 26863196 MeRIP-seq:(Medium) rs1334681647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465068,Human_RBP_ID_8816912 104001 RMVar_ID_104001 Human_SNP_ID_615372303 m1A Human chr17 + 3724006 3724006 3724006 CCGCACATATGGGGCTGCGGACGGCAGGAGACAGCGGCGGCCGGGCCGGGAAGCCGCGCAGTGGT CCGCACATATGGGGCTGCGGACGGCAGGAGACGGCGGCGGCCGGGCCGGGAAGCCGCGCAGTGGT A G HASPIN Ensembl:ENSG00000177602 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3723966..3724536 26863196 MeRIP-seq:(Medium) rs1410085252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465068 104002 RMVar_ID_104002 Human_SNP_ID_615372370 m1A Human chr17 + 3724126 3724126 3724126 CATCGGCGACCCCTCGCAGTCCGACGATCCTGACGATCCCGACGACCCCGACTTCCCCGGCAGCC CATCGGCGACCCCTCGCAGTCCGACGATCCTGGCGATCCCGACGACCCCGACTTCCCCGGCAGCC A G HASPIN Ensembl:ENSG00000177602 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:3724076..3724270 26863196 MeRIP-seq:(Medium) rs371254692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269924,Human_RBP_ID_278171,Human_RBP_ID_1007659,Human_RBP_ID_1181560,Human_RBP_ID_1286048,Human_RBP_ID_1368092,Human_RBP_ID_1532727,Human_RBP_ID_3521504,Human_RBP_ID_4421961,Human_RBP_ID_5260048,Human_RBP_ID_5275064,Human_RBP_ID_5420021,Human_RBP_ID_5441356,Human_RBP_ID_5466393,Human_RBP_ID_5496920,Human_RBP_ID_6589554,Human_RBP_ID_8089867,Human_RBP_ID_8253360,Human_RBP_ID_8450967,Human_RBP_ID_8816913,Human_RBP_ID_9071589,Human_RBP_ID_9257392,Human_RBP_ID_9287318,Human_RBP_ID_12988367,Human_RBP_ID_17004571,Human_RBP_ID_17259376,Human_RBP_ID_17375280,Human_RBP_ID_17490768,Human_RBP_ID_17691864,Human_RBP_ID_17890858,Human_RBP_ID_18291590,Human_RBP_ID_18438834,Human_RBP_ID_18513612,Human_RBP_ID_18530599,Human_RBP_ID_18696016,Human_RBP_ID_19031071,Human_RBP_ID_21889630,Human_RBP_ID_21926919,Human_RBP_ID_22422065,Human_RBP_ID_22499294,Human_RBP_ID_23129138,Human_RBP_ID_23275575,Human_RBP_ID_23308227,Human_RBP_ID_24531820,Human_RBP_ID_24538813,Human_RBP_ID_24540043,Human_RBP_ID_26641986,Human_RBP_ID_27253059,Human_RBP_ID_27451369,Human_RBP_ID_27560958,Human_RBP_ID_27664547 104003 RMVar_ID_104003 Human_SNP_ID_615372471 m1A Human chr17 - 3724295 3724295 3724295 CCGCAGGGTGTGCTGCACTTCTGCGGGGGCCGAGCTCGCAGCCCCAGGCGTCTTGGGGTCACGGT CCGCAGGGTGTGCTGCACTTCTGCGGGGGCCGGGCTCGCAGCCCCAGGCGTCTTGGGGTCACGGT T C ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3724251..3724352 26863196 MeRIP-seq:(Medium) rs1367996805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 104004 RMVar_ID_104004 Human_SNP_ID_615373283 m1A Human chr17 + 3726404 3726404 3726404 GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCATCCCCACAGGAGGGTGGAACTCCCATTCTCAC GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCCTCCCCACAGGAGGGTGGAACTCCCATTCTCAC A C HASPIN Ensembl:ENSG00000177602 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs170208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17259380,Human_RBP_ID_17375284,Human_RBP_ID_17490771 GWAS_ID_13449 104005 RMVar_ID_104005 Human_SNP_ID_615373284 m1A Human chr17 + 3726404 3726404 3726404 GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCATCCCCACAGGAGGGTGGAACTCCCATTCTCAC GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCGTCCCCACAGGAGGGTGGAACTCCCATTCTCAC A G HASPIN Ensembl:ENSG00000177602 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs170208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17259380,Human_RBP_ID_17375284,Human_RBP_ID_17490771 GWAS_ID_13449 104006 RMVar_ID_104006 Human_SNP_ID_615397930 m1A Human chr17 + 3808537 3808537 3808537 GTTGGTGAGGGGAAGATTGAGGCGGGAGGGGGAGAAGCCTGGGCGGAAGCATGTCACTGGAGGTA GTTGGTGAGGGGAAGATTGAGGCGGGAGGGGGGGAAGCCTGGGCGGAAGCATGTCACTGGAGGTA A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:3808527..3808658 26863196 MeRIP-seq:(Medium) rs1024542051 Functional Loss SNV dbSNP153 33..33 33 - - - 104007 RMVar_ID_104007 Human_SNP_ID_615400567 m1A Human chr17 + 3818475 3818475 3818475 AGCTCCTCGTGGTACTCTACCACCACTCTGTCATCTGCATCCATGTCCTGGTCTTCTTCTTCCTC AGCTCCTCGTGGTACTCTACCACCACTCTGTCGTCTGCATCCATGTCCTGGTCTTCTTCTTCCTC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3818424..3818534 26863196 MeRIP-seq:(Medium) rs773526709 Functional Loss SNV dbSNP153 33..33 33 - - - 104008 RMVar_ID_104008 Human_SNP_ID_615400570 m1A Human chr17 - 3818486 3818486 3818486 AGGAAGAGGAAGAGGAAGAAGAAGACCAGGACATGGATGCAGATGACAGAGTGGTGGTAGAGTAC AGGAAGAGGAAGAGGAAGAAGAAGACCAGGACGTGGATGCAGATGACAGAGTGGTGGTAGAGTAC T C NCBP3 Ensembl:ENSG00000074356 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3818436..3818605 26863196 MeRIP-seq:(Medium) rs763105788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235714,Human_RBP_ID_819421,Human_RBP_ID_899112,Human_RBP_ID_1181650,Human_RBP_ID_1546625,Human_RBP_ID_4423300,Human_RBP_ID_6590677,Human_RBP_ID_8232118,Human_RBP_ID_8817139,Human_RBP_ID_9375117,Human_RBP_ID_18990030,Human_RBP_ID_22950760,Human_RBP_ID_23118732,Human_RBP_ID_24544758,Human_RBP_ID_25341592,Human_RBP_ID_26331052,Human_RBP_ID_27812168 Human_Splice_Rec_1762044,Human_Splice_Rec_1762060,Human_Splice_Rec_1762078,Human_Splice_Rec_1762090 RMVar_hsa_circ_78681,RMVar_hsa_circ_328692,RMVar_hsa_circ_338607,RMVar_hsa_circ_269867,RMVar_hsa_circ_361062,RMVar_hsa_circ_181334 104009 RMVar_ID_104009 Human_SNP_ID_615400572 m1A Human chr17 - 3818496 3818493 3818496 GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGAAGACCAGGACATGGATGCAGATGACAGAGTGGT GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGA___CCAGGACATGGATGCAGATGACAGAGTGGT GTCT G NCBP3 Ensembl:ENSG00000074356 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3818409..3818589 26863196 MeRIP-seq:(Medium) rs746673147 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_235714,Human_RBP_ID_819421,Human_RBP_ID_899112,Human_RBP_ID_1181650,Human_RBP_ID_1546625,Human_RBP_ID_4423300,Human_RBP_ID_6590677,Human_RBP_ID_8232118,Human_RBP_ID_9375117,Human_RBP_ID_18990031,Human_RBP_ID_22950761,Human_RBP_ID_23118732,Human_RBP_ID_24544758,Human_RBP_ID_25341592,Human_RBP_ID_26331052,Human_RBP_ID_27812168 Human_Splice_Rec_1762044,Human_Splice_Rec_1762060,Human_Splice_Rec_1762078,Human_Splice_Rec_1762090 RMVar_hsa_circ_78681,RMVar_hsa_circ_328692,RMVar_hsa_circ_338607,RMVar_hsa_circ_269867,RMVar_hsa_circ_361062,RMVar_hsa_circ_181334 104010 RMVar_ID_104010 Human_SNP_ID_615400574 m1A Human chr17 - 3818496 3818496 3818496 GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGAAGACCAGGACATGGATGCAGATGACAGAGTGGT GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGACGACCAGGACATGGATGCAGATGACAGAGTGGT T G NCBP3 Ensembl:ENSG00000074356 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3818409..3818589 26863196 MeRIP-seq:(Medium) rs1200647023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235714,Human_RBP_ID_819421,Human_RBP_ID_899112,Human_RBP_ID_1181650,Human_RBP_ID_1546625,Human_RBP_ID_4423300,Human_RBP_ID_6590677,Human_RBP_ID_8232118,Human_RBP_ID_9375117,Human_RBP_ID_18990031,Human_RBP_ID_22950761,Human_RBP_ID_23118732,Human_RBP_ID_24544758,Human_RBP_ID_25341592,Human_RBP_ID_26331052,Human_RBP_ID_27812168 Human_Splice_Rec_1762044,Human_Splice_Rec_1762060,Human_Splice_Rec_1762078,Human_Splice_Rec_1762090 RMVar_hsa_circ_78681,RMVar_hsa_circ_328692,RMVar_hsa_circ_338607,RMVar_hsa_circ_269867,RMVar_hsa_circ_361062,RMVar_hsa_circ_181334 104011 RMVar_ID_104011 Human_SNP_ID_615408236 m1A Human chr17 + 3845768 3845768 3845768 CCTCACTCACCTCCTTGCACAGCGCGGCTCAGAGGGGGCAGCGGAGGGGGGTCCTCAACTCCCTC CCTCACTCACCTCCTTGCACAGCGCGGCTCAGGGGGGGCAGCGGAGGGGGGTCCTCAACTCCCTC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3845767..3845928 26863196 MeRIP-seq:(Medium) rs1271050279 Functional Loss SNV dbSNP153 33..33 33 - - - 104012 RMVar_ID_104012 Human_SNP_ID_615408363 m1A Human chr17 + 3846129 3846129 3846129 CCACCTCCATGGGCTCCGGCTCGCCACGGTCAACACCGGACTCCGCCTCAGGGGACGGGAGCCCC CCACCTCCATGGGCTCCGGCTCGCCACGGTCAGCACCGGACTCCGCCTCAGGGGACGGGAGCCCC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:3846026..3846150 32194978 MeRIP-seq:(Medium) rs1253750376 Functional Loss SNV dbSNP153 33..33 33 - - - 104013 RMVar_ID_104013 Human_SNP_ID_615408400 m1A Human chr17 + 3846192 3846192 3846192 CCAGGGCCGGCCCCGCCGGGGCCTCCGCCTTCACCGACACCCGCAGGCCCCGTACGGCCGCCATC CCAGGGCCGGCCCCGCCGGGGCCTCCGCCTTCGCCGACACCCGCAGGCCCCGTACGGCCGCCATC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:3846026..3846230;chr17:3845970..3846250;chr17:3846026..3846250 26863196 MeRIP-seq:(Medium) rs1030271100 Functional Loss SNV dbSNP153 33..33 33 - - - 104014 RMVar_ID_104014 Human_SNP_ID_615413464 m1A Human chr17 - 3862172 3862172 3862172 GCATGCACCCAGGGCCACCCGGCAGCACACTCATCCCGCGCCTCCAGAGGCCCACCCCTCATGCA GCATGCACCCAGGGCCACCCGGCAGCACACTCTTCCCGCGCCTCCAGAGGCCCACCCCTCATGCA T A CAMKK1 Ensembl:ENSG00000004660 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:3862121..3862253 26863196 MeRIP-seq:(Medium) rs973257861 Functional Loss SNV dbSNP153 33..33 33 - - - 104015 RMVar_ID_104015 Human_SNP_ID_615416027 m1A Human chr17 + 3869574 3869571 3869575 ACCTCCACCACGCTGCAGTGCTCCTCCTCCGAAGGAAGGGGCTCCTCCCCGTTCTTGGTCACCCA ACCTCCACCACGCTGCAGTGCTCCTCCTCC____GAAGGGGCTCCTCCCCGTTCTTGGTCACCCA CGAAG C lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:3869526..3869575 26863196 MeRIP-seq:(Medium) rs1467416330 Functional Loss DEL dbSNP153 31..34 33 - - - 104016 RMVar_ID_104016 Human_SNP_ID_615417739 m1A Human chr17 - 3873881 3873881 3873881 GGGCCTCTGTGTGGGCAGGGGCTGTTTGCAATATCAGGAAGAAGGTGGATTATGAGGAGAAGGGA GGGCCTCTGTGTGGGCAGGGGCTGTTTGCAATGTCAGGAAGAAGGTGGATTATGAGGAGAAGGGA T C CAMKK1 Ensembl:ENSG00000004660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3873866..3874079 26863196 MeRIP-seq:(Medium) rs1277563997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2505341 RMVar_hsa_circ_36300,RMVar_hsa_circ_103349,RMVar_hsa_circ_120784,RMVar_hsa_circ_181338,RMVar_hsa_circ_111997,RMVar_hsa_circ_181340,RMVar_hsa_circ_125137,RMVar_hsa_circ_181341,RMVar_hsa_circ_181342 104017 RMVar_ID_104017 Human_SNP_ID_615419240 m1A Human chr17 + 3879539 3879539 3879539 TGGCCCGGACAGTGTTTCCAGCATCATCTTTCACTAACCACGGCCCTCCTCTGCCCACTGGAGGC TGGCCCGGACAGTGTTTCCAGCATCATCTTTCGCTAACCACGGCCCTCCTCTGCCCACTGGAGGC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3879504..3879631 26863196 MeRIP-seq:(Medium) rs571855514 Functional Loss SNV dbSNP153 33..33 33 - - - 104018 RMVar_ID_104018 Human_SNP_ID_615422915 m1A Human chr17 - 3892232 3892232 3892232 TGGAGTGGTGTGTGAGGGCGGGTCACGCGGACACGGGCGTGTGCCTGTCAGGGGAGGGGGTGTGC TGGAGTGGTGTGTGAGGGCGGGTCACGCGGACGCGGGCGTGTGCCTGTCAGGGGAGGGGGTGTGC T C CAMKK1 Ensembl:ENSG00000004660 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3892182..3892381 26863196 MeRIP-seq:(Medium) rs114858913 Functional Loss SNV dbSNP153 33..33 33 - - - 104019 RMVar_ID_104019 Human_SNP_ID_615423049 m1A Human chr17 + 3892677 3892677 3892677 TGCACCGGGGATGGATGCGGTCCGCAGACAGAAGCGGGGAAGAACGCAGACGGCGGGGCACCCGC TGCACCGGGGATGGATGCGGTCCGCAGACAGAGGCGGGGAAGAACGCAGACGGCGGGGCACCCGC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3892671..3892989 26863196 MeRIP-seq:(Medium) rs1035073057 Functional Loss SNV dbSNP153 33..33 33 - - - 104020 RMVar_ID_104020 Human_SNP_ID_615445002 m1A Human chr17 - 3964287 3964287 3964287 GGACGGCGCAGACGGCCGGGCGGGCGGCATGGAGGCGGCGCATCTGCTCCCGGCCGCCGACGTGC GGACGGCGCAGACGGCCGGGCGGGCGGCATGGGGGCGGCGCATCTGCTCCCGGCCGCCGACGTGC T C ATP2A3 Ensembl:ENSG00000074370 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:3964236..3964384 26863196 MeRIP-seq:(Medium) rs1024702610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465070 104021 RMVar_ID_104021 Human_SNP_ID_615457083 m1A Human chr17 + 4007482 4007482 4007482 CAGGGAGACGTGTCAGGGAGAAACGTCAGGACACTGGTGCAGTACACTCAACAGGCTGTGGGGGG CAGGGAGACGTGTCAGGGAGAAACGTCAGGACGCTGGTGCAGTACACTCAACAGGCTGTGGGGGG A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4007433..4007505 26863196 MeRIP-seq:(Medium) rs1192860686 Functional Loss SNV dbSNP153 33..33 33 - - - 104022 RMVar_ID_104022 Human_SNP_ID_615481408 m1A Human chr17 - 4094784 4094784 4094784 AGCAGCAGTGCAGAGATGTGGACCAAGAGACCACTAGGAGGGAGAAGCGACAGGACCTGGTGATT AGCAGCAGTGCAGAGATGTGGACCAAGAGACCGCTAGGAGGGAGAAGCGACAGGACCTGGTGATT T C ZZEF1 Ensembl:ENSG00000074755 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4094709..4094851 26863196 MeRIP-seq:(Medium) rs1467112498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108418,RMVar_hsa_circ_181377,RMVar_hsa_circ_264957,RMVar_hsa_circ_265620,RMVar_hsa_circ_13971,RMVar_hsa_circ_181393,RMVar_hsa_circ_78498,RMVar_hsa_circ_94934,RMVar_hsa_circ_374738,RMVar_hsa_circ_265046,RMVar_hsa_circ_36615,RMVar_hsa_circ_22858,RMVar_hsa_circ_181395,RMVar_hsa_circ_181396,RMVar_hsa_circ_326672,RMVar_hsa_circ_85998,RMVar_hsa_circ_181403,RMVar_hsa_circ_2559 104023 RMVar_ID_104023 Human_SNP_ID_615495130 m1A Human chr17 - 4142909 4142909 4142909 GGCGGCGGCGGCGGCTGCAGAGCCAGGCGCCCAAGACGGAGACCCCATGGGGAACGCTCCGAGTC GGCGGCGGCGGCGGCTGCAGAGCCAGGCGCCCGAGACGGAGACCCCATGGGGAACGCTCCGAGTC T C ZZEF1 Ensembl:ENSG00000074755 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4142864..4142948 26863196 MeRIP-seq:(Medium) rs973712358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464236 RMVar_hsa_circ_265046,RMVar_hsa_circ_85998,RMVar_hsa_circ_181403,RMVar_hsa_circ_266926,RMVar_hsa_circ_113982,RMVar_hsa_circ_181408 104024 RMVar_ID_104024 Human_SNP_ID_615495131 m1A Human chr17 - 4142909 4142909 4142909 GGCGGCGGCGGCGGCTGCAGAGCCAGGCGCCCAAGACGGAGACCCCATGGGGAACGCTCCGAGTC GGCGGCGGCGGCGGCTGCAGAGCCAGGCGCCCCAGACGGAGACCCCATGGGGAACGCTCCGAGTC T G ZZEF1 Ensembl:ENSG00000074755 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4142864..4142948 26863196 MeRIP-seq:(Medium) rs973712358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464236 RMVar_hsa_circ_265046,RMVar_hsa_circ_85998,RMVar_hsa_circ_181403,RMVar_hsa_circ_266926,RMVar_hsa_circ_113982,RMVar_hsa_circ_181408 104025 RMVar_ID_104025 Human_SNP_ID_615495567 m1A Human chr17 - 4143759 4143759 4143759 GCCCAACAAAAGCCCACGGCCTCCGCACCTCAACATCTATATAGGCCCACCCGCTCCGCACTTCC GCCCAACAAAAGCCCACGGCCTCCGCACCTCAGCATCTATATAGGCCCACCCGCTCCGCACTTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4143552..4143903 26863196 MeRIP-seq:(Medium) rs144617379 Functional Loss SNV dbSNP153 33..33 33 - - - 104026 RMVar_ID_104026 Human_SNP_ID_615495579 m1A Human chr17 + 4143770 4143770 4143770 GCGGGTGGGCCTATATAGATGTTGAGGTGCGGAGGCCGTGGGCTTTTGTTGGGCCTGGCTGTAGC GCGGGTGGGCCTATATAGATGTTGAGGTGCGGCGGCCGTGGGCTTTTGTTGGGCCTGGCTGTAGC A C CYB5D2 Ensembl:ENSG00000167740 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4143754..4143869 26863196 MeRIP-seq:(Medium) rs370488302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6595176,Human_RBP_ID_13007185,Human_RBP_ID_23129259 104027 RMVar_ID_104027 Human_SNP_ID_615496890 m1A Human chr17 - 4148076 4148076 4148076 CCTTTCTCACCTGAACTCCTACAGCAAACCTCAAGGAAGCCCTCCCTGCATTCATTCTTGCCCCA CCTTTCTCACCTGAACTCCTACAGCAAACCTCCAGGAAGCCCTCCCTGCATTCATTCTTGCCCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4147982..4148226 26863196 MeRIP-seq:(Medium) rs1027475144 Functional Loss SNV dbSNP153 33..33 33 - - - 104028 RMVar_ID_104028 Human_SNP_ID_615499556 m1A Human chr17 + 4158105 4158105 4158105 GGCAGACCCGTGCTCACTGCCCCTGTCCCCTCACTGGCAGACCCGTGCTCACTGCCCCTGTCCCC GGCAGACCCGTGCTCACTGCCCCTGTCCCCTCGCTGGCAGACCCGTGCTCACTGCCCCTGTCCCC A G CYB5D2 Ensembl:ENSG00000167740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4158055..4158226 26863196 MeRIP-seq:(Medium) rs1187230544 Functional Loss SNV dbSNP153 33..33 33 - - - 104029 RMVar_ID_104029 Human_SNP_ID_615500133 m1A Human chr17 + 4160104 4160078 4160105 TCCACATGACTCAGCGCCGTACCCCTATATCCACGACTCAGCTCCGTACCCCTATATCCACATGA TCCACAT___________________________GACTCAGCTCCGTACCCCTATATCCACATGA TGACTCAGCGCCGTACCCCTATATCCAC T CYB5D2 Ensembl:ENSG00000167740 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4160053..4160198 26863196 MeRIP-seq:(Medium) rs1406178605 Functional Loss DEL dbSNP153 8..34 33 - - - 104030 RMVar_ID_104030 Human_SNP_ID_615500195 m1A Human chr17 + 4160190 4160164 4160191 TCCACATGACTCAGCTCCGTACCCCTATATCCACGACCCAGCTCCGTACCCCTATAATCCACATG TCCACAT___________________________GACCCAGCTCCGTACCCCTATAATCCACATG TGACTCAGCTCCGTACCCCTATATCCAC T CYB5D2 Ensembl:ENSG00000167740 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4159960..4160257 26863196 MeRIP-seq:(Medium) rs1567894362 Functional Loss DEL dbSNP153 8..34 33 - - - 104031 RMVar_ID_104031 Human_SNP_ID_615500216 m1A Human chr17 + 4160211 4160211 4160211 CCCCTATATCCACGACCCAGCTCCGTACCCCTATAATCCACATGACTCAGCTCCGTACCCCTGTA CCCCTATATCCACGACCCAGCTCCGTACCCCTGTAATCCACATGACTCAGCTCCGTACCCCTGTA A G CYB5D2 Ensembl:ENSG00000167740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4160075..4160310 26863196 MeRIP-seq:(Medium) rs1312616241 Functional Loss SNV dbSNP153 33..33 33 - - - 104032 RMVar_ID_104032 Human_SNP_ID_615521708 m1A Human chr17 + 4242422 4242422 4242422 CAGCTTGACATACTCCTGCCGCAGAAGCATCAAGTGCTTCTCCAACTTGGCCACCTCCTCTGCAA CAGCTTGACATACTCCTGCCGCAGAAGCATCATGTGCTTCTCCAACTTGGCCACCTCCTCTGCAA A T lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4242305..4242428 26863196 MeRIP-seq:(Medium) rs937521295 Functional Loss SNV dbSNP153 33..33 33 - - - 104033 RMVar_ID_104033 Human_SNP_ID_615527319 m1A Human chr17 + 4264117 4264117 4264117 CGGAGGGGGTTGCTGGACTCTGGGGGAAGCGGAGAGCCGGGTTTCTTTTTACCGGGTATTTTTGA CGGAGGGGGTTGCTGGACTCTGGGGGAAGCGGGGAGCCGGGTTTCTTTTTACCGGGTATTTTTGA A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4264067..4264546 26863196 MeRIP-seq:(Medium) rs1398859002 Functional Loss SNV dbSNP153 33..33 33 - - - 104034 RMVar_ID_104034 Human_SNP_ID_615530454 m1A Human chr17 - 4276062 4276062 4276062 GTAGAGATGAAGATCTGTTTGGTGTAGAGAGCAGTACTTACCAGGGCAAGGACAACTTGGAGACT GTAGAGATGAAGATCTGTTTGGTGTAGAGAGCGGTACTTACCAGGGCAAGGACAACTTGGAGACT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4276052..4276139 26863196 MeRIP-seq:(Medium) rs375867974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13017994 RMVar_hsa_circ_181450,RMVar_hsa_circ_95830,RMVar_hsa_circ_112621,RMVar_hsa_circ_181451 104035 RMVar_ID_104035 Human_SNP_ID_615538755 m1A Human chr17 - 4307122 4307122 4307122 ATGTATTGATTAAACTTTTCTTTTTCCACAGAACTCAACAAAAATCCAGTGGAAGGCTTTTCTGC ATGTATTGATTAAACTTTTCTTTTTCCACAGACCTCAACAAAAATCCAGTGGAAGGCTTTTCTGC T G UBE2G1 Ensembl:ENSG00000132388 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4307099..4307173 26863196 MeRIP-seq:(Medium) rs763731364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903803,Human_RBP_ID_18439062 Human_Splice_Rec_1763128,Human_Splice_Rec_1763140,Human_Splice_Rec_1763150,Human_Splice_Rec_1763156,Human_Splice_Rec_1763164,Human_Splice_Rec_1763176 Human_miRNA_ID_2969486 RMVar_hsa_circ_181450,RMVar_hsa_circ_95830,RMVar_hsa_circ_112621,RMVar_hsa_circ_181451,RMVar_hsa_circ_181458,RMVar_hsa_circ_279866,RMVar_hsa_circ_305510,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_333304,RMVar_hsa_circ_33765,RMVar_hsa_circ_181460,RMVar_hsa_circ_297315,RMVar_hsa_circ_338088,RMVar_hsa_circ_181459,RMVar_hsa_circ_181466,RMVar_hsa_circ_181468,RMVar_hsa_circ_317979,RMVar_hsa_circ_377756,RMVar_hsa_circ_344151,RMVar_hsa_circ_306396,RMVar_hsa_circ_181467 104036 RMVar_ID_104036 Human_SNP_ID_615607739 m1A Human chr17 + 4536764 4536764 4536764 TCTCTCTCCTCTCCCCACCCCTGGGCTCTCCCATCTCCCCCTGGGGCTGACGAGGTCCCTGCCCA TCTCTCTCCTCTCCCCACCCCTGGGCTCTCCCCTCTCCCCCTGGGGCTGACGAGGTCCCTGCCCA A C SPNS2 Ensembl:ENSG00000183018 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4536713..4536840 26863196 MeRIP-seq:(Medium) rs1459893157 Functional Loss SNV dbSNP153 33..33 33 - - - 104037 RMVar_ID_104037 Human_SNP_ID_615609230 m1A Human chr17 - 4539442 4539442 4539442 AGCCTGCTTCAGAGTGGGGCCAAGAAGAAAGCACAGGTGAGGAAGGCAGGGAAGCCCTGAGCACA AGCCTGCTTCAGAGTGGGGCCAAGAAGAAAGCGCAGGTGAGGAAGGCAGGGAAGCCCTGAGCACA T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4539392..4539592 32194978 MeRIP-seq:(Medium) rs771811645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4474326,Human_RBP_ID_6603559,Human_RBP_ID_13041209,Human_RBP_ID_22062989 Human_Splice_Rec_1763365,Human_Splice_Rec_1763427,Human_Splice_Rec_1763491 RMVar_hsa_circ_43361 104038 RMVar_ID_104038 Human_SNP_ID_615609233 m1A Human chr17 - 4539450 4539450 4539450 GGAGTCCCAGCCTGCTTCAGAGTGGGGCCAAGAAGAAAGCACAGGTGAGGAAGGCAGGGAAGCCC GGAGTCCCAGCCTGCTTCAGAGTGGGGCCAAGGAGAAAGCACAGGTGAGGAAGGCAGGGAAGCCC T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4539399..4539482 32194978 MeRIP-seq:(Medium) rs112418856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1860405,Human_RBP_ID_4474327,Human_RBP_ID_6603561,Human_RBP_ID_9375130,Human_RBP_ID_22062989,Human_RBP_ID_22805034,Human_RBP_ID_26811827,Human_RBP_ID_26963567 Human_Splice_Rec_1763365,Human_Splice_Rec_1763427,Human_Splice_Rec_1763491 RMVar_hsa_circ_43361 104039 RMVar_ID_104039 Human_SNP_ID_615609502 m1A Human chr17 - 4539900 4539897 4539900 TCCCCAGTGCCACCCAGAGCCCCATCAGTAAGAAGCGGAAGAAAAAGGGATTCTTGCCAGAGACG TCCCCAGTGCCACCCAGAGCCCCATCAGTAAG___CGGAAGAAAAAGGGATTCTTGCCAGAGACG GCTT G MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4539851..4539900 32194978 MeRIP-seq:(Medium) rs1567601710 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_50606,Human_RBP_ID_18469954,Human_RBP_ID_26331072 Human_Splice_Rec_1763364,Human_Splice_Rec_1763378,Human_Splice_Rec_1763426,Human_Splice_Rec_1763478,Human_Splice_Rec_1763484,Human_Splice_Rec_1763506,Human_Splice_Rec_1763510,Human_Splice_Rec_1763512 RMVar_hsa_circ_43361 104040 RMVar_ID_104040 Human_SNP_ID_615609504 m1A Human chr17 - 4539900 4539900 4539900 TCCCCAGTGCCACCCAGAGCCCCATCAGTAAGAAGCGGAAGAAAAAGGGATTCTTGCCAGAGACG TCCCCAGTGCCACCCAGAGCCCCATCAGTAAGTAGCGGAAGAAAAAGGGATTCTTGCCAGAGACG T A MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4539851..4539900 32194978 MeRIP-seq:(Medium) rs1179496149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50606,Human_RBP_ID_18469954,Human_RBP_ID_26331072 Human_Splice_Rec_1763364,Human_Splice_Rec_1763378,Human_Splice_Rec_1763426,Human_Splice_Rec_1763478,Human_Splice_Rec_1763484,Human_Splice_Rec_1763506,Human_Splice_Rec_1763510,Human_Splice_Rec_1763512 RMVar_hsa_circ_43361 104041 RMVar_ID_104041 Human_SNP_ID_615609529 m1A Human chr17 + 4539932 4539932 4539932 TCTTACTGATGGGGCTCTGGGTGGCACTGGGGATCTCCTTGGCATCCTTCTTCTCCAACTTGGGG TCTTACTGATGGGGCTCTGGGTGGCACTGGGGGTCTCCTTGGCATCCTTCTTCTCCAACTTGGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:4539610..4539955;chr17:4539690..4541595 26863196,32194978 MeRIP-seq:(Medium) rs1235634050 Functional Loss SNV dbSNP153 33..33 33 - - - 104042 RMVar_ID_104042 Human_SNP_ID_615610925 m1A Human chr17 - 4542720 4542720 4542720 CCCTGGCCTAGGCTGCCAGCTGCTTGGACTTGAACCTGGTGACCCGGGTGTACTCGACAGCACTG CCCTGGCCTAGGCTGCCAGCTGCTTGGACTTGTACCTGGTGACCCGGGTGTACTCGACAGCACTG T A MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4542527..4543129 32194978 MeRIP-seq:(Medium) rs1320024892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535516,Human_RBP_ID_1860416,Human_RBP_ID_13041253,Human_RBP_ID_18700179,Human_RBP_ID_27156580 Human_Splice_Rec_1763354,Human_Splice_Rec_1763368,Human_Splice_Rec_1763416,Human_Splice_Rec_1763468,Human_Splice_Rec_1763496 RMVar_hsa_circ_792,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 104043 RMVar_ID_104043 Human_SNP_ID_615612017 m1A Human chr17 - 4544818 4544818 4544818 CAGCCTCTTTGCCGAGCAGAAGCTGCGTATCCAGGCCCGGCGAGACGAGAAGAACAAGCTGCAGA CAGCCTCTTTGCCGAGCAGAAGCTGCGTATCCGGGCCCGGCGAGACGAGAAGAACAAGCTGCAGA T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4544664..4544919 32194978 MeRIP-seq:(Medium) rs758404966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236180,Human_RBP_ID_5525257 Human_Splice_Rec_1763349,Human_Splice_Rec_1763411,Human_Splice_Rec_1763463 RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 104044 RMVar_ID_104044 Human_SNP_ID_615612262 m1A Human chr17 - 4545096 4545094 4545097 GGAGAGCGAGGGGGAGGAGAGCGAGGAGGAGGAGCGCGACGGGGACGTGGATCAGGGCTTCCGGG GGAGAGCGAGGGGGAGGAGAGCGAGGAGGAG___CGCGACGGGGACGTGGATCAGGGCTTCCGGG GCTC G MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4544797..4545733 26863196 MeRIP-seq:(Medium) rs779065720 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_47993,Human_RBP_ID_765274,Human_RBP_ID_822141,Human_RBP_ID_896109,Human_RBP_ID_3949942,Human_RBP_ID_5648781,Human_RBP_ID_6603586,Human_RBP_ID_9288682,Human_RBP_ID_9327135,Human_RBP_ID_18990071,Human_RBP_ID_26781910 Human_Splice_Rec_1763346,Human_Splice_Rec_1763347,Human_Splice_Rec_1763408,Human_Splice_Rec_1763409,Human_Splice_Rec_1763460,Human_Splice_Rec_1763461,Human_Splice_Rec_1763519 RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 104045 RMVar_ID_104045 Human_SNP_ID_615612549 m1A Human chr17 - 4545644 4545644 4545644 GGCCCGGAGCGTGTTTGGCCACATCTGCTCCCACCTGACCCCGCGTGCCCTGCAGCTAATTCTGG GGCCCGGAGCGTGTTTGGCCACATCTGCTCCCTCCTGACCCCGCGTGCCCTGCAGCTAATTCTGG T A MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:4544958..4545925 26863196 MeRIP-seq:(Medium) rs1485374863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491574,Human_RBP_ID_6603590,Human_RBP_ID_8454762,Human_RBP_ID_8818784,Human_RBP_ID_18700191,Human_RBP_ID_22443340 Human_Splice_Rec_1763343,Human_Splice_Rec_1763405,Human_Splice_Rec_1763457,Human_Splice_Rec_1763517 Human_miRNA_ID_2391881 RMVar_hsa_circ_181472,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470,RMVar_hsa_circ_87855,RMVar_hsa_circ_93725,RMVar_hsa_circ_181473 104046 RMVar_ID_104046 Human_SNP_ID_615612687 m1A Human chr17 - 4545858 4545858 4545858 AAAGTCTGGGAGAGAAGCCCCGCCGGAGCCGCACCAAGACCATCGGTGGGTCCTTGGTCACGAGA AAAGTCTGGGAGAGAAGCCCCGCCGGAGCCGCCCCAAGACCATCGGTGGGTCCTTGGTCACGAGA T G MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4545577..4545875 26863196 MeRIP-seq:(Medium) rs760138795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3949943,Human_RBP_ID_18990073 Human_Splice_Rec_1763340,Human_Splice_Rec_1763341,Human_Splice_Rec_1763402,Human_Splice_Rec_1763403,Human_Splice_Rec_1763454,Human_Splice_Rec_1763455,Human_Splice_Rec_1763515 RMVar_hsa_circ_181472,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470,RMVar_hsa_circ_87855,RMVar_hsa_circ_93725,RMVar_hsa_circ_181473 104047 RMVar_ID_104047 Human_SNP_ID_615612704 m1A Human chr17 - 4545888 4545887 4545889 TGCTGGGTGACATCCAGACCTGCATCAGGAAAAGTCTGGGAGAGAAGCCCCGCCGGAGCCGCACC TGCTGGGTGACATCCAGACCTGCATCAGGAA__GTCTGGGAGAGAAGCCCCGCCGGAGCCGCACC CTT C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4545171..4547708 32194978 MeRIP-seq:(Medium) rs754373825 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_301097,Human_RBP_ID_1860422,Human_RBP_ID_3949943,Human_RBP_ID_18990073 Human_Splice_Rec_1763340,Human_Splice_Rec_1763341,Human_Splice_Rec_1763402,Human_Splice_Rec_1763403,Human_Splice_Rec_1763454,Human_Splice_Rec_1763455,Human_Splice_Rec_1763515 RMVar_hsa_circ_181472,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470,RMVar_hsa_circ_87855,RMVar_hsa_circ_93725,RMVar_hsa_circ_181473 104048 RMVar_ID_104048 Human_SNP_ID_615616431 m1A Human chr17 - 4555201 4555201 4555201 ACAGTCGCGAGTTCTTGGACTTCTTCTGGGACATTGCGAAGCCTGAGCAGGAGACGCGACTTGCG ACAGTCGCGAGTTCTTGGACTTCTTCTGGGACGTTGCGAAGCCTGAGCAGGAGACGCGACTTGCG T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:4555151..4555350 26863196 MeRIP-seq:(Medium) rs1332354204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48006,Human_RBP_ID_1535559,Human_RBP_ID_1860464,Human_RBP_ID_4433250,Human_RBP_ID_8818804,Human_RBP_ID_18700238,Human_RBP_ID_22215701,Human_RBP_ID_22805053,Human_RBP_ID_26963681 Human_Splice_Rec_1763315,Human_Splice_Rec_1763429,Human_Splice_Rec_1763529 RMVar_hsa_circ_83134,RMVar_hsa_circ_181480 104049 RMVar_ID_104049 Human_SNP_ID_615616514 m1A Human chr17 - 4555326 4555326 4555326 ACACGTGTTTCGTGTTTCGGTGAGTGTGGCGGAGATGGAGAGCCGGGATCCCGCCCAGCCGATGT ACACGTGTTTCGTGTTTCGGTGAGTGTGGCGGGGATGGAGAGCCGGGATCCCGCCCAGCCGATGT T C MYBBP1A Ensembl:ENSG00000132382 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4555126..4555375 26863196 MeRIP-seq:(Medium) rs552756664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535561,Human_RBP_ID_8824333,Human_RBP_ID_9289728,Human_RBP_ID_18419513,Human_RBP_ID_22444245,Human_RBP_ID_23730434 RMVar_hsa_circ_83134,RMVar_hsa_circ_181480 104050 RMVar_ID_104050 Human_SNP_ID_615651707 m1A Human chr17 - 4671456 4671456 4671456 GTCCCCCTGATGATGAGAAGCCACCACCTCCCACAGAGCCTGACTCCTAGCCATCTTCTGCACCC GTCCCCCTGATGATGAGAAGCCACCACCTCCCTCAGAGCCTGACTCCTAGCCATCTTCTGCACCC T A PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9436 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1860994,Human_RBP_ID_5577434,Human_RBP_ID_6605636,Human_RBP_ID_8455122,Human_RBP_ID_9375140,Human_RBP_ID_18700622,Human_RBP_ID_20172378,Human_RBP_ID_26330627,Human_RBP_ID_26964058,Human_RBP_ID_27813317 Human_Splice_Rec_1763728,Human_Splice_Rec_1763760,Human_Splice_Rec_1763792,Human_Splice_Rec_1763826,Human_Splice_Rec_1763856,Human_Splice_Rec_1763890 Human_miRNA_ID_3069833 GWAS_ID_13450,GWAS_ID_13451,GWAS_ID_13452,GWAS_ID_13453,GWAS_ID_13454 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_118384,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_78929,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181490,RMVar_hsa_circ_181491,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483 104051 RMVar_ID_104051 Human_SNP_ID_615651954 m1A Human chr17 + 4672024 4672024 4672024 TCGGGTTCTGGCTGCACCTTTGGGGGAGACTCAGGGGGAGGCAGAGCTGGAGGCAGGGTTGGGGG TCGGGTTCTGGCTGCACCTTTGGGGGAGACTCCGGGGGAGGCAGAGCTGGAGGCAGGGTTGGGGG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:4671999..4672225 26863196 MeRIP-seq:(Medium) rs768800721 Functional Loss SNV dbSNP153 33..33 33 - - - 104052 RMVar_ID_104052 Human_SNP_ID_615651955 m1A Human chr17 + 4672024 4672024 4672024 TCGGGTTCTGGCTGCACCTTTGGGGGAGACTCAGGGGGAGGCAGAGCTGGAGGCAGGGTTGGGGG TCGGGTTCTGGCTGCACCTTTGGGGGAGACTCGGGGGGAGGCAGAGCTGGAGGCAGGGTTGGGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:4671999..4672225 26863196 MeRIP-seq:(Medium) rs768800721 Functional Loss SNV dbSNP153 33..33 33 - - - 104053 RMVar_ID_104053 Human_SNP_ID_615652026 m1A Human chr17 - 4672196 4672196 4672196 TGAAGAGGAAGAAGAGGAGGAAGAAGAGTTTGAGGAAGAATTTGAGGAAGAAGAAGGTGAGTTAG TGAAGAGGAAGAAGAGGAGGAAGAAGAGTTTGGGGAAGAATTTGAGGAAGAAGAAGGTGAGTTAG T C PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:4671726..4672500;chr17:4671917..4672450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_48498,Human_RBP_ID_199966,Human_RBP_ID_278311,Human_RBP_ID_896110,Human_RBP_ID_1546626,Human_RBP_ID_1861042,Human_RBP_ID_2510521,Human_RBP_ID_4474555,Human_RBP_ID_5525263,Human_RBP_ID_6605715,Human_RBP_ID_9444044,Human_RBP_ID_22415849,Human_RBP_ID_22959157,Human_RBP_ID_23114369,Human_RBP_ID_23118734,Human_RBP_ID_24544762,Human_RBP_ID_25343493,Human_RBP_ID_26331085,Human_RBP_ID_26964087 Human_Splice_Rec_1763823,Human_Splice_Rec_1763887 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_78929,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181490,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483,RMVar_hsa_circ_81526,RMVar_hsa_circ_181492 104054 RMVar_ID_104054 Human_SNP_ID_615652027 m1A Human chr17 - 4672202 4672200 4672203 ATATTTTGAAGAGGAAGAAGAGGAGGAAGAAGAGTTTGAGGAAGAATTTGAGGAAGAAGAAGGTG ATATTTTGAAGAGGAAGAAGAGGAGGAAGAA___TTTGAGGAAGAATTTGAGGAAGAAGAAGGTG ACTC A PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4671934..4673474;chr17:4671805..4672550 26863196 MeRIP-seq:(Medium) rs755794262 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_48498,Human_RBP_ID_199966,Human_RBP_ID_896110,Human_RBP_ID_1546626,Human_RBP_ID_2510521,Human_RBP_ID_4474555,Human_RBP_ID_5525263,Human_RBP_ID_6605715,Human_RBP_ID_9444044,Human_RBP_ID_22959157,Human_RBP_ID_23114369,Human_RBP_ID_23118734,Human_RBP_ID_24544762,Human_RBP_ID_25343493,Human_RBP_ID_26331085 Human_Splice_Rec_1763823,Human_Splice_Rec_1763887 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_78929,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181490,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483,RMVar_hsa_circ_81526,RMVar_hsa_circ_181492 104055 RMVar_ID_104055 Human_SNP_ID_615652369 m1A Human chr17 + 4672858 4672858 4672858 CGGGGAGGGACAGACACTAGGCCTGGGACAGAAAGGCCTAGGTGGTTGGCTGTGGTGGGAGGTCC CGGGGAGGGACAGACACTAGGCCTGGGACAGATAGGCCTAGGTGGTTGGCTGTGGTGGGAGGTCC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4672750..4673150 26863196 MeRIP-seq:(Medium) rs765929440 Functional Loss SNV dbSNP153 33..33 33 - - - 104056 RMVar_ID_104056 Human_SNP_ID_615652396 m1A Human chr17 + 4672909 4672909 4672909 GTGGTGGGAGGTCCAGGGCGTGCCGAGGGCACAGGGCCTGCTGAGGGCATGGGGCCTGCTGAAGG GTGGTGGGAGGTCCAGGGCGTGCCGAGGGCACGGGGCCTGCTGAGGGCATGGGGCCTGCTGAAGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:4672701..4673475 26863196 MeRIP-seq:(Medium) rs750760710 Functional Loss SNV dbSNP153 33..33 33 - - - 104057 RMVar_ID_104057 Human_SNP_ID_615652422 m1A Human chr17 - 4672933 4672933 4672933 TCCATGCCCTCAGCAGGCCCCATGCCTTCAGCAGGCCCCATGCCCTCAGCAGGCCCTGTGCCCTC TCCATGCCCTCAGCAGGCCCCATGCCTTCAGCGGGCCCCATGCCCTCAGCAGGCCCTGTGCCCTC T C PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4672776..4673075 26863410 MeRIP-seq:(Medium) rs1170755948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48501,Human_RBP_ID_9375148 Human_miRNA_ID_1093562,Human_miRNA_ID_2493738,Human_miRNA_ID_2512858,Human_miRNA_ID_2512859,Human_miRNA_ID_2696091,Human_miRNA_ID_3055681,Human_miRNA_ID_3055682 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_78929,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181490,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483,RMVar_hsa_circ_81526,RMVar_hsa_circ_181492 104058 RMVar_ID_104058 Human_SNP_ID_615652570 m1A Human chr17 - 4673260 4673260 4673260 CCTGCAAGCCTTCTCCCTCGGCCAGCGAGAAGATAGCCTTGAGGTAACTGTGATGGGCCAAGCCC CCTGCAAGCCTTCTCCCTCGGCCAGCGAGAAGGTAGCCTTGAGGTAACTGTGATGGGCCAAGCCC T C PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4673251..4673300 26863196 MeRIP-seq:(Medium) rs752922209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8455227,Human_RBP_ID_9377345,Human_RBP_ID_18700715,Human_RBP_ID_22805166,Human_RBP_ID_27813323 Human_Splice_Rec_1763725,Human_Splice_Rec_1763757,Human_Splice_Rec_1763789,Human_Splice_Rec_1763821,Human_Splice_Rec_1763853,Human_Splice_Rec_1763885,Human_Splice_Rec_1763891 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483,RMVar_hsa_circ_100946,RMVar_hsa_circ_81526,RMVar_hsa_circ_181492,RMVar_hsa_circ_181493 104059 RMVar_ID_104059 Human_SNP_ID_615652621 m1A Human chr17 + 4673393 4673393 4673393 TTCACGGCGGCAGCGGGAGCTCGTGTACGGGGAGCTGCCTAGGACCTCACCCTGCTGTACACCCA TTCACGGCGGCAGCGGGAGCTCGTGTACGGGGGGCTGCCTAGGACCTCACCCTGCTGTACACCCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4673238..4673476 26863196 MeRIP-seq:(Medium) rs1167726482 Functional Loss SNV dbSNP153 33..33 33 - - - 104060 RMVar_ID_104060 Human_SNP_ID_615652981 m1A Human chr17 + 4674590 4674590 4674590 TCCGGTGGCTTGGCGGGGCCATAGCTTCCCCCACATCCAGCTTTAGCTTCTTGGGGGCGCTAGGC TCCGGTGGCTTGGCGGGGCCATAGCTTCCCCCGCATCCAGCTTTAGCTTCTTGGGGGCGCTAGGC A G AC091153.2 Ensembl:ENSG00000235085 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4672821..4674650 32194978 MeRIP-seq:(Medium) rs769818141 Functional Loss SNV dbSNP153 33..33 33 - - - 104061 RMVar_ID_104061 Human_SNP_ID_615653596 m1A Human chr17 + 4676229 4676229 4676229 TCTTCCATCCCCTCCTCTGTCATTTCTGGTGGACGACCTGCCTGTATTCTAACCCATTTTCCCCA TCTTCCATCCCCTCCTCTGTCATTTCTGGTGGGCGACCTGCCTGTATTCTAACCCATTTTCCCCA A G AC091153.2 Ensembl:ENSG00000235085 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4676181..4676344 26863196 MeRIP-seq:(Medium) rs1226270048 Functional Loss SNV dbSNP153 33..33 33 - - - 104062 RMVar_ID_104062 Human_SNP_ID_615661370 m1A Human chr17 - 4703975 4703975 4703975 GCTGCTGCTGGAGAGTGTTTCTGGTTTGCTGCAACCTCGAACGGGGTCTGCCGTTGCTCCGGTGC GCTGCTGCTGGAGAGTGTTTCTGGTTTGCTGCGACCTCGAACGGGGTCTGCCGTTGCTCCGGTGC T C PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4703926..4704050 32194978 MeRIP-seq:(Medium) rs867782035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465077,Human_RBP_ID_9326426,Human_RBP_ID_18700866 104063 RMVar_ID_104063 Human_SNP_ID_615661371 m1A Human chr17 - 4703975 4703975 4703975 GCTGCTGCTGGAGAGTGTTTCTGGTTTGCTGCAACCTCGAACGGGGTCTGCCGTTGCTCCGGTGC GCTGCTGCTGGAGAGTGTTTCTGGTTTGCTGCCACCTCGAACGGGGTCTGCCGTTGCTCCGGTGC T G PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4703926..4704050 32194978 MeRIP-seq:(Medium) rs867782035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465077,Human_RBP_ID_9326426,Human_RBP_ID_18700866 104064 RMVar_ID_104064 Human_SNP_ID_615661402 m1A Human chr17 - 4704030 4704030 4704030 TTCCTGGCGGGACCGGGGGTCTCTCGGCAGTGAGCTCGGGCCCGCGGCTCCGCCTGCTGCTGCTG TTCCTGGCGGGACCGGGGGTCTCTCGGCAGTGGGCTCGGGCCCGCGGCTCCGCCTGCTGCTGCTG T C PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4703951..4704125 26863410 MeRIP-seq:(Medium) rs1036218087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50666,Human_RBP_ID_4465078,Human_RBP_ID_5237850,Human_RBP_ID_5366040,Human_RBP_ID_5466597,Human_RBP_ID_9287715,Human_RBP_ID_9326426,Human_RBP_ID_18439191,Human_RBP_ID_22060961,Human_RBP_ID_22587499 Human_miRNA_ID_598642,Human_miRNA_ID_1045430 104065 RMVar_ID_104065 Human_SNP_ID_615661451 m1A Human chr17 + 4704091 4704091 4704091 GGAACCCCAGCCGCGGAGCCCGCAGAGGGCCCACTCAGAACGGCTGCCGCCATCTTCCCCCGGGT GGAACCCCAGCCGCGGAGCCCGCAGAGGGCCCGCTCAGAACGGCTGCCGCCATCTTCCCCCGGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4703968..4704125 26863196 MeRIP-seq:(Medium) rs1300796605 Functional Loss SNV dbSNP153 33..33 33 - - - 104066 RMVar_ID_104066 Human_SNP_ID_615661576 m1A Human chr17 + 4704272 4704272 4704272 GGCTCAAGCTGGGAAGGAGCATGCGCGGAGAGAGCAGCCTGGGCGCCGAGGCAGCGGGGTGCTCG GGCTCAAGCTGGGAAGGAGCATGCGCGGAGAGCGCAGCCTGGGCGCCGAGGCAGCGGGGTGCTCG A C AC091153.3 Ensembl:ENSG00000244184 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4704222..4704376 26863196 MeRIP-seq:(Medium) rs1267705425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1763951 104067 RMVar_ID_104067 Human_SNP_ID_615661582 m1A Human chr17 - 4704279 4704279 4704279 CGGGAACCGAGCACCCCGCTGCCTCGGCGCCCAGGCTGCTCTCTCCGCGCATGCTCCTTCCCAGC CGGGAACCGAGCACCCCGCTGCCTCGGCGCCCTGGCTGCTCTCTCCGCGCATGCTCCTTCCCAGC T A PELP1 Ensembl:ENSG00000141456 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4704201..4705199;chr17:4704229..4704350 26863196 MeRIP-seq:(Medium) rs987569899 Functional Loss SNV dbSNP153 33..33 33 - - - 104068 RMVar_ID_104068 Human_SNP_ID_615661755 m1A Human chr17 + 4704757 4704757 4704757 AAAGTGCTGAGATTACAGGCATGAGCCACCGCACCCTGCCTAGGAATCAGTAACGTGTGTGTGTG AAAGTGCTGAGATTACAGGCATGAGCCACCGCGCCCTGCCTAGGAATCAGTAACGTGTGTGTGTG A G AC091153.3 Ensembl:ENSG00000244184 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7225717 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13455 104069 RMVar_ID_104069 Human_SNP_ID_615661882 m1A Human chr17 - 4705184 4705177 4705184 CGGCCGAGGAAGGCATTGCTGCTGGAGGGGTAATGGATGTTAATACTGCTTCACAAGAGGTGCTG CGGCCGAGGAAGGCATTGCTGCTGGAGGGGTA_______TTAATACTGCTTCACAAGAGGTGCTG ACATCCAT A AC091153.1 Ensembl:ENSG00000213939 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4705179..4705255 26863196 MeRIP-seq:(Medium) rs1246436646 Functional Loss DEL dbSNP153 33..39 33 - - - Human_miRNA_ID_1910563 104070 RMVar_ID_104070 Human_SNP_ID_615664757 m1A Human chr17 + 4710695 4710695 4710695 CAGCGGGCGAGGAGGCTGCGAGCGAGCCGCGAACCGAGCGGGCGGCGGGCGCGCGCACCATGGGG CAGCGGGCGAGGAGGCTGCGAGCGAGCCGCGAGCCGAGCGGGCGGCGGGCGCGCGCACCATGGGG A G ARRB2 Ensembl:ENSG00000141480 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:4710651..4710803 26863196 MeRIP-seq:(Medium) rs938156015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465945 Human_Splice_Rec_1763953,Human_Splice_Rec_1763967,Human_Splice_Rec_1763993,Human_Splice_Rec_1764003,Human_Splice_Rec_1764013,Human_Splice_Rec_1764041,Human_Splice_Rec_1764067,Human_Splice_Rec_1764091,Human_Splice_Rec_1764097,Human_Splice_Rec_1764105,Human_Splice_Rec_1764113,Human_Splice_Rec_1764123,Human_Splice_Rec_1764129,Human_Splice_Rec_1764155,Human_Splice_Rec_1764183,Human_Splice_Rec_1764199,Human_Splice_Rec_1764227 104071 RMVar_ID_104071 Human_SNP_ID_615664772 m1A Human chr17 + 4710732 4710732 4710732 GCGGGCGGCGGGCGCGCGCACCATGGGGGAGAAACCCGGGACCAGGTAAGGGAGGTGGGGCCACG GCGGGCGGCGGGCGCGCGCACCATGGGGGAGAGACCCGGGACCAGGTAAGGGAGGTGGGGCCACG A G ARRB2 Ensembl:ENSG00000141480 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:4710556..4710798 26863196 MeRIP-seq:(Medium) rs1177660966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465945 Human_Splice_Rec_1763953,Human_Splice_Rec_1763967,Human_Splice_Rec_1763993,Human_Splice_Rec_1764003,Human_Splice_Rec_1764013,Human_Splice_Rec_1764041,Human_Splice_Rec_1764067,Human_Splice_Rec_1764091,Human_Splice_Rec_1764097,Human_Splice_Rec_1764105,Human_Splice_Rec_1764113,Human_Splice_Rec_1764123,Human_Splice_Rec_1764129,Human_Splice_Rec_1764155,Human_Splice_Rec_1764183,Human_Splice_Rec_1764199,Human_Splice_Rec_1764227 104072 RMVar_ID_104072 Human_SNP_ID_615664773 m1A Human chr17 + 4710733 4710733 4710733 CGGGCGGCGGGCGCGCGCACCATGGGGGAGAAACCCGGGACCAGGTAAGGGAGGTGGGGCCACGC CGGGCGGCGGGCGCGCGCACCATGGGGGAGAAGCCCGGGACCAGGTAAGGGAGGTGGGGCCACGC A G ARRB2 Ensembl:ENSG00000141480 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:4710637..4710800 26863410 MeRIP-seq:(Medium) rs1412242437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465945 Human_Splice_Rec_1763953,Human_Splice_Rec_1763967,Human_Splice_Rec_1763993,Human_Splice_Rec_1764003,Human_Splice_Rec_1764013,Human_Splice_Rec_1764041,Human_Splice_Rec_1764067,Human_Splice_Rec_1764091,Human_Splice_Rec_1764097,Human_Splice_Rec_1764105,Human_Splice_Rec_1764113,Human_Splice_Rec_1764123,Human_Splice_Rec_1764129,Human_Splice_Rec_1764155,Human_Splice_Rec_1764183,Human_Splice_Rec_1764199,Human_Splice_Rec_1764227 104073 RMVar_ID_104073 Human_SNP_ID_615666319 m1A Human chr17 - 4716128 4716128 4716128 AAGCACCACGCCATCTAGGAGGGGGACACACCAGCTCACTTCCTGAAAGGGCCGCTCCCCGCTTT AAGCACCACGCCATCTAGGAGGGGGACACACCTGCTCACTTCCTGAAAGGGCCGCTCCCCGCTTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4716126..4716200 26863196 MeRIP-seq:(Medium) rs1312957690 Functional Loss SNV dbSNP153 33..33 33 - - - 104074 RMVar_ID_104074 Human_SNP_ID_615666452 m1A Human chr17 + 4716546 4716546 4716546 TCCCCCCGGTGCCCAACCCACCCCGGCCCCCCACCCGCCTGCAGGACCGGCTGCTGAGGAAGCTG TCCCCCCGGTGCCCAACCCACCCCGGCCCCCCCCCCGCCTGCAGGACCGGCTGCTGAGGAAGCTG A C ARRB2 Ensembl:ENSG00000141480 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4716398..4716603 26863196 MeRIP-seq:(Medium) rs747331573 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_492296,Human_RBP_ID_4474815 Human_Splice_Rec_1763973,Human_Splice_Rec_1764007,Human_Splice_Rec_1764021,Human_Splice_Rec_1764047,Human_Splice_Rec_1764071,Human_Splice_Rec_1764103,Human_Splice_Rec_1764135,Human_Splice_Rec_1764187,Human_Splice_Rec_1764207,Human_Splice_Rec_1764233,Human_Splice_Rec_1764251 104075 RMVar_ID_104075 Human_SNP_ID_615667667 m1A Human chr17 + 4720373 4720373 4720373 CTCTCTAGTCCCATGTCGTCGTCCTCTTCACGATGCCTCTCCCCTTCCCCAGGGATGTCTCTGTG CTCTCTAGTCCCATGTCGTCGTCCTCTTCACGCTGCCTCTCCCCTTCCCCAGGGATGTCTCTGTG A C ARRB2 Ensembl:ENSG00000141480 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4720371..4720953 32194978 MeRIP-seq:(Medium) rs1171604410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1763989,Human_Splice_Rec_1764037,Human_Splice_Rec_1764063,Human_Splice_Rec_1764087,Human_Splice_Rec_1764151,Human_Splice_Rec_1764179,Human_Splice_Rec_1764223,Human_Splice_Rec_1764267 RMVar_hsa_circ_371798,RMVar_hsa_circ_181504 104076 RMVar_ID_104076 Human_SNP_ID_615673365 m1A Human chr17 - 4739784 4739781 4739784 GGATCGGGGAAGTGAAAGTGCCTCGGAGGAGGAGGGCCGGTCCGGCAGTGCAGCCGCCTCACAGG GGATCGGGGAAGTGAAAGTGCCTCGGAGGAGG___GCCGGTCCGGCAGTGCAGCCGCCTCACAGG CCCT C CXCL16 Ensembl:ENSG00000161921 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4739733..4739863 26863196 MeRIP-seq:(Medium) rs1452069756 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_822062,Human_RBP_ID_4464245,Human_RBP_ID_6606878 RMVar_hsa_circ_124118,RMVar_hsa_circ_181507 104077 RMVar_ID_104077 Human_SNP_ID_615687652 m1A Human chr17 + 4789102 4789100 4789102 TCGCTATCTTCGCGCTGCTGCTGCTTTATCTCAGTGTTCGGAGCCTAGGTGAGCTGCCCCTTCCC TCGCTATCTTCGCGCTGCTGCTGCTTTATCT__GTGTTCGGAGCCTAGGTGAGCTGCCCCTTCCC TCA T GLTPD2,AC233723.2 Ensembl:ENSG00000182327,Ensembl:ENSG00000280254 Protein coding,Other CDS,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4789098..4789183 26863196 MeRIP-seq:(Medium) - Functional Loss DEL HGVD 32..33 33 - - - Human_RBP_ID_4464249,Human_RBP_ID_5144001 Human_Splice_Rec_1764475 104078 RMVar_ID_104078 Human_SNP_ID_615688023 m1A Human chr17 - 4789889 4789889 4789889 CGGCTGCTCCAGCAGTCCCGCCCTCCGCTCCCACGCCGCCATGGCCACCAGCGACCAGTAGTGCT CGGCTGCTCCAGCAGTCCCGCCCTCCGCTCCCTCGCCGCCATGGCCACCAGCGACCAGTAGTGCT T A lnc-VMO1-1,lnc-VMO1-1:2 RNACentral:URS00009BB8E4,RNACentral:URS00009B26D6 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4789887..4790236;chr17:4789879..4790018 26863196 MeRIP-seq:(Medium) rs1381852804 Functional Loss SNV dbSNP153 33..33 33 - - - 104079 RMVar_ID_104079 Human_SNP_ID_615688034 m1A Human chr17 + 4789914 4789914 4789914 GGCGGCGTGGGAGCGGAGGGCGGGACTGCTGGAGCAGCCGGGGGCGGCCCCCCGGGACCCGACCC GGCGGCGTGGGAGCGGAGGGCGGGACTGCTGGGGCAGCCGGGGGCGGCCCCCCGGGACCCGACCC A G GLTPD2 Ensembl:ENSG00000182327 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4789904..4789994 26863196 MeRIP-seq:(Medium) rs753915329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17669819,Human_RBP_ID_18990112,Human_RBP_ID_22443352 104080 RMVar_ID_104080 Human_SNP_ID_615688217 m1A Human chr17 - 4790163 4790163 4790163 CCGCCTCGGTGGCTCCGGGACACGCCAGCTCCAGCAGGCGGCGGCGACCCGGGAAGGCGAGGAAG CCGCCTCGGTGGCTCCGGGACACGCCAGCTCCTGCAGGCGGCGGCGACCCGGGAAGGCGAGGAAG T A lnc-VMO1-1,lnc-VMO1-1:2 RNACentral:URS00009BB8E4,RNACentral:URS00009B26D6 lincRNA,lincRNA exon,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4790063..4790208 26863410 MeRIP-seq:(Medium) rs1337649247 Functional Loss SNV dbSNP153 33..33 33 - - - 104081 RMVar_ID_104081 Human_SNP_ID_615690711 m1A Human chr17 - 4797777 4797777 4797777 GCCCTCCTTCTTGAGGGTCCCAGCCTGCGATGATGATTCCCGCCATCAGGTCTTCCCGGTATCGG GCCCTCCTTCTTGAGGGTCCCAGCCTGCGATGGTGATTCCCGCCATCAGGTCTTCCCGGTATCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4797726..4797836 26863196 MeRIP-seq:(Medium) rs1191482242 Functional Loss SNV dbSNP153 33..33 33 - - - 104082 RMVar_ID_104082 Human_SNP_ID_615690782 m1A Human chr17 - 4797981 4797981 4797981 TACACCTGCCAGATAGAAGGAGAGGAGTCACCAGTCGTATCCTCCCTCCAACACACGTACATTCA TACACCTGCCAGATAGAAGGAGAGGAGTCACCGGTCGTATCCTCCCTCCAACACACGTACATTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4797978..4798177 26863196 MeRIP-seq:(Medium) rs1350303241 Functional Loss SNV dbSNP153 33..33 33 - - - 104083 RMVar_ID_104083 Human_SNP_ID_615693413 m1A Human chr17 + 4807223 4807223 4807223 CGGAACCCCCGCGGGCGCTGGCTCCGTCTGCCAGGGTGAGGGGGCCGGGAAGGGGCGCGCGGGGG CGGAACCCCCGCGGGCGCTGGCTCCGTCTGCCTGGGTGAGGGGGCCGGGAAGGGGCGCGCGGGGG A T PLD2 Ensembl:ENSG00000129219 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4807221..4807315;chr17:4807219..4807392 26863196 MeRIP-seq:(Medium) rs1429878902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419833,Human_RBP_ID_19081133 Human_Splice_Rec_1764519,Human_Splice_Rec_1764567,Human_Splice_Rec_1764615,Human_Splice_Rec_1764649 104084 RMVar_ID_104084 Human_SNP_ID_615694756 m1A Human chr17 - 4811142 4811142 4811142 GGTCAGAAGAGATGACCAAGTTTGGGGGTCAGAAAGGTCGGCGCGAAATCAGAGAGATCAATGTG GGTCAGAAGAGATGACCAAGTTTGGGGGTCAGGAAGGTCGGCGCGAAATCAGAGAGATCAATGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4811104..4811202 26863196 MeRIP-seq:(Medium) rs994493086 Functional Loss SNV dbSNP153 33..33 33 - - - 104085 RMVar_ID_104085 Human_SNP_ID_615696860 m1A Human chr17 - 4818136 4818136 4818136 TCCCCAGGTCTCTCTCCTGGGACACCCCTTCCATGCTCTCCCCCACCTCCTCCCAGTCAGACCTC TCCCCAGGTCTCTCTCCTGGGACACCCCTTCCGTGCTCTCCCCCACCTCCTCCCAGTCAGACCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4818129..4818244 26863196 MeRIP-seq:(Medium) rs777551441 Functional Loss SNV dbSNP153 33..33 33 - - - 104086 RMVar_ID_104086 Human_SNP_ID_615697354 m1A Human chr17 + 4819289 4819289 4819289 TGGGGACAGGCGAAGAGATGAGAGGCAGGATGACAGAGACTGCAGCTGAGGCTCGTGTAGGGGTG TGGGGACAGGCGAAGAGATGAGAGGCAGGATGTCAGAGACTGCAGCTGAGGCTCGTGTAGGGGTG A T PLD2 Ensembl:ENSG00000129219 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4819281..4819402 26863196 MeRIP-seq:(Medium) rs1455153936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127582,RMVar_hsa_circ_181519,RMVar_hsa_circ_181520 104087 RMVar_ID_104087 Human_SNP_ID_615701599 m1A Human chr17 + 4833526 4833526 4833526 TTCTCCGATGGGGGAGAAGCGGCGACGGCGGCAGTGGAGTAACCGAGCCGGAGCGTGAGCGGCCC TTCTCCGATGGGGGAGAAGCGGCGACGGCGGCGGTGGAGTAACCGAGCCGGAGCGTGAGCGGCCC A G MINK1 Ensembl:ENSG00000141503 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4833424..4833530 26863410 MeRIP-seq:(Medium) rs900393301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464251,Human_RBP_ID_5184876,Human_RBP_ID_20291782 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006 104088 RMVar_ID_104088 Human_SNP_ID_615706404 m1A Human chr17 + 4852395 4852395 4852395 ATCAATCACAAAAATGTAATTGGTGTCACGAAAGAGTCAGTACAGGGTATTGTGGGAGGAGAGGA ATCAATCACAAAAATGTAATTGGTGTCACGAAGGAGTCAGTACAGGGTATTGTGGGAGGAGAGGA A G MINK1 Ensembl:ENSG00000141503 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4852391..4852563 26863196 MeRIP-seq:(Medium) rs1325905406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23733269 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006 104089 RMVar_ID_104089 Human_SNP_ID_615706801 m1A Human chr17 + 4853270 4853270 4853270 GGTTGGTGGGAAGAGTGTGGTTGGTGGGGGGAATGTGGTTGGTAGGTAGAGTGGTTGGTGGGGGA GGTTGGTGGGAAGAGTGTGGTTGGTGGGGGGAGTGTGGTTGGTAGGTAGAGTGGTTGGTGGGGGA A G MINK1 Ensembl:ENSG00000141503 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4853266..4853573 26863196 MeRIP-seq:(Medium) rs1274064474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8189248,Human_RBP_ID_9423271,Human_RBP_ID_23733271 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006 104090 RMVar_ID_104090 Human_SNP_ID_615706881 m1A Human chr17 - 4853452 4853452 4853452 CCCCCACCAACCACACTCTTCCCACCAACCACACTCCCCCCACCAACCACACTCCCCCTCAACCA CCCCCACCAACCACACTCTTCCCACCAACCACCCTCCCCCCACCAACCACACTCCCCCTCAACCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4853450..4853545 26863196 MeRIP-seq:(Medium) rs1433531194 Functional Loss SNV dbSNP153 33..33 33 - - - 104091 RMVar_ID_104091 Human_SNP_ID_615708674 m1A Human chr17 - 4860065 4859963 4860065 GCTCCGCATGCGGCAAGTAGTTCCCGGACGCGACCCTTCCCCCTGTACCCCGCTCCGCATGGGGC GCTCCGCATGCGGCAAGTAGTTCCCGGACGCG_________________________________ GCGCGTCCGGGAACTACTTGCCGCATGCGGAGCGGGGTACAGAGGGAAGGGGCGCGTCCGGGAACTACTGGCCCCATGCGGAGCGGGGTACAGGGGGAAGGGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4860064..4860177 26863196 MeRIP-seq:(Medium) rs1567575579 Functional Loss DEL dbSNP153 33..65 33 - - - 104092 RMVar_ID_104092 Human_SNP_ID_615708730 m1A Human chr17 - 4860065 4860065 4860065 GCTCCGCATGCGGCAAGTAGTTCCCGGACGCGACCCTTCCCCCTGTACCCCGCTCCGCATGGGGC GCTCCGCATGCGGCAAGTAGTTCCCGGACGCGCCCCTTCCCCCTGTACCCCGCTCCGCATGGGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4860064..4860177 26863196 MeRIP-seq:(Medium) rs1200890488 Functional Loss SNV dbSNP153 33..33 33 - - - 104093 RMVar_ID_104093 Human_SNP_ID_615712732 m1A Human chr17 + 4874499 4874499 4874499 CCATTTTGGAAGAGTTAAATCAGTGGCAGCAGAAGGAAGACATGGGGGAGGCTAGAGTTCCAGGA CCATTTTGGAAGAGTTAAATCAGTGGCAGCAGGAGGAAGACATGGGGGAGGCTAGAGTTCCAGGA A G MINK1 Ensembl:ENSG00000141503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4874496..4874678 26863196 MeRIP-seq:(Medium) rs73973643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181523,RMVar_hsa_circ_111006 104094 RMVar_ID_104094 Human_SNP_ID_615712733 m1A Human chr17 + 4874499 4874499 4874499 CCATTTTGGAAGAGTTAAATCAGTGGCAGCAGAAGGAAGACATGGGGGAGGCTAGAGTTCCAGGA CCATTTTGGAAGAGTTAAATCAGTGGCAGCAGTAGGAAGACATGGGGGAGGCTAGAGTTCCAGGA A T MINK1 Ensembl:ENSG00000141503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4874496..4874678 26863196 MeRIP-seq:(Medium) rs73973643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181523,RMVar_hsa_circ_111006 104095 RMVar_ID_104095 Human_SNP_ID_615715921 m1A Human chr17 + 4886625 4886625 4886625 ATTGACCGATCCCGGAAGAAGCGGGGTGAGAAAGGTCAGTGGGCAGGCTGGAGGGGGCAGGTACT ATTGACCGATCCCGGAAGAAGCGGGGTGAGAACGGTCAGTGGGCAGGCTGGAGGGGGCAGGTACT A C MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4886502..4886666 26863196 MeRIP-seq:(Medium) rs1252573064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18990133,Human_RBP_ID_26331096 Human_Splice_Rec_1764739,Human_Splice_Rec_1764861,Human_Splice_Rec_1764925,Human_Splice_Rec_1764985,Human_Splice_Rec_1765047,Human_Splice_Rec_1765083 RMVar_hsa_circ_67687,RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_5493,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_39851,RMVar_hsa_circ_107944,RMVar_hsa_circ_181527 104096 RMVar_ID_104096 Human_SNP_ID_615716828 m1A Human chr17 + 4889732 4889729 4889732 GCGGCTGGAGGACATGCAGGCTCTGCGGCGGGAGGAGGAGCGGCGGCAGGCGGAGCGCGAGCAGG GCGGCTGGAGGACATGCAGGCTCTGCGGCG___GGAGGAGCGGCGGCAGGCGGAGCGCGAGCAGG GGGA G MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4887567..4889780;chr17:4889614..4889775 26863196 MeRIP-seq:(Medium) rs1358960432 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_48521,Human_RBP_ID_3949956,Human_RBP_ID_9346134,Human_RBP_ID_9375167,Human_RBP_ID_18987681,Human_RBP_ID_22959555 Human_Splice_Rec_1764744,Human_Splice_Rec_1764745,Human_Splice_Rec_1764806,Human_Splice_Rec_1764866,Human_Splice_Rec_1764867,Human_Splice_Rec_1764930,Human_Splice_Rec_1764931,Human_Splice_Rec_1764990,Human_Splice_Rec_1764991,Human_Splice_Rec_1765052,Human_Splice_Rec_1765053,Human_Splice_Rec_1765088,Human_Splice_Rec_1765089 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_39851,RMVar_hsa_circ_107944,RMVar_hsa_circ_99825,RMVar_hsa_circ_181527,RMVar_hsa_circ_181528 104097 RMVar_ID_104097 Human_SNP_ID_615717116 m1A Human chr17 + 4890478 4890478 4890478 GAGAGGGCATGCCTGCTCTAACTCCCAGGGCCACACCCTGCTGAGCCCTCTCTCCCTACCCTTGG GAGAGGGCATGCCTGCTCTAACTCCCAGGGCCCCACCCTGCTGAGCCCTCTCTCCCTACCCTTGG A C MINK1 Ensembl:ENSG00000141503 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4890475..4890600 26863196 MeRIP-seq:(Medium) rs1165086645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765512,Human_RBP_ID_822463,Human_RBP_ID_896120,Human_RBP_ID_5362423,Human_RBP_ID_9377374,Human_RBP_ID_22542805,Human_RBP_ID_22655716,Human_RBP_ID_26334032 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_39851,RMVar_hsa_circ_107944,RMVar_hsa_circ_99825,RMVar_hsa_circ_181527,RMVar_hsa_circ_181528 104098 RMVar_ID_104098 Human_SNP_ID_615717620 m1A Human chr17 + 4891582 4891582 4891582 CCTTCCCAGCCTCCCATGACCCCGACCCTGCCATCCCCGCACCCACTGCCACGCCCAGTGCCCGA CCTTCCCAGCCTCCCATGACCCCGACCCTGCCCTCCCCGCACCCACTGCCACGCCCAGTGCCCGA A C MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4891450..4891675 26863196 MeRIP-seq:(Medium) rs377766100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765513 Human_Splice_Rec_1764810,Human_Splice_Rec_1764996 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_39851,RMVar_hsa_circ_107944,RMVar_hsa_circ_99825,RMVar_hsa_circ_181527,RMVar_hsa_circ_181528 104099 RMVar_ID_104099 Human_SNP_ID_615718044 m1A Human chr17 - 4892428 4892428 4892428 GGGTGCCCCGCTCTGCCCGCCTTTGCAGATAGATTTGCCAGGCGGAGTTGCTGCGAGGTCTGTGA GGGTGCCCCGCTCTGCCCGCCTTTGCAGATAGGTTTGCCAGGCGGAGTTGCTGCGAGGTCTGTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4892400..4892538 26863196 MeRIP-seq:(Medium) rs763247682 Functional Loss SNV dbSNP153 33..33 33 - - - 104100 RMVar_ID_104100 Human_SNP_ID_615718628 m1A Human chr17 + 4893526 4893526 4893526 ATGGACTACTCGTCGTCCAGCGAGGAGGTGGAAAGCAGTGAGGACGACGAGGAGGAAGGCGAAGG ATGGACTACTCGTCGTCCAGCGAGGAGGTGGACAGCAGTGAGGACGACGAGGAGGAAGGCGAAGG A C MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4893426..4893618 26863196 MeRIP-seq:(Medium) rs776245677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5577475,Human_RBP_ID_9377382,Human_RBP_ID_18990148,Human_RBP_ID_22959334,Human_RBP_ID_23114444 Human_Splice_Rec_1764760,Human_Splice_Rec_1764761,Human_Splice_Rec_1764820,Human_Splice_Rec_1764821,Human_Splice_Rec_1764882,Human_Splice_Rec_1764883,Human_Splice_Rec_1764944,Human_Splice_Rec_1764945,Human_Splice_Rec_1765006,Human_Splice_Rec_1765007,Human_Splice_Rec_1765104,Human_Splice_Rec_1765105,Human_Splice_Rec_1765132 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_98539,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_181529 104101 RMVar_ID_104101 Human_SNP_ID_615718924 m1A Human chr17 - 4894238 4894236 4894239 TGTTCTCGGTGGGTGAGTGGCTGGGCTGGACCACGTCAGGCAGGTTTGTGTACCCATTGCTGTCA TGTTCTCGGTGGGTGAGTGGCTGGGCTGGAC___GTCAGGCAGGTTTGTGTACCCATTGCTGTCA CGTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4894160..4894242 26863196 MeRIP-seq:(Medium) rs747828789 Functional Loss DEL dbSNP153 32..34 33 - - - 104102 RMVar_ID_104102 Human_SNP_ID_615719265 m1A Human chr17 + 4895155 4895155 4895155 TGAGGAAGGGTTCTGTGGTCAACGTGAATCCCACCAACACCCGGGCCCACAGTGAGACCCCTGAG TGAGGAAGGGTTCTGTGGTCAACGTGAATCCCCCCAACACCCGGGCCCACAGTGAGACCCCTGAG A C MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4895104..4895205 32194978 MeRIP-seq:(Medium) rs1461018466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48530,Human_RBP_ID_899184,Human_RBP_ID_18701799,Human_RBP_ID_18990152 Human_Splice_Rec_1764768,Human_Splice_Rec_1764769,Human_Splice_Rec_1764828,Human_Splice_Rec_1764829,Human_Splice_Rec_1764890,Human_Splice_Rec_1764891,Human_Splice_Rec_1764952,Human_Splice_Rec_1764953,Human_Splice_Rec_1765014,Human_Splice_Rec_1765015,Human_Splice_Rec_1765112,Human_Splice_Rec_1765113,Human_Splice_Rec_1765135,Human_Splice_Rec_1765143 Human_miRNA_ID_729912,Human_miRNA_ID_1703130 RMVar_hsa_circ_1097,RMVar_hsa_circ_98539,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_4642,RMVar_hsa_circ_92454,RMVar_hsa_circ_181529,RMVar_hsa_circ_181530,RMVar_hsa_circ_20709 104103 RMVar_ID_104103 Human_SNP_ID_615719518 m1A Human chr17 + 4895755 4895755 4895755 TTACCTGTCCTGGCTCCGGAACAAGATTCTGCACAATGACCCAGAAGTGGAGAAGAAGCAGGGCT TTACCTGTCCTGGCTCCGGAACAAGATTCTGCGCAATGACCCAGAAGTGGAGAAGAAGCAGGGCT A G MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4895682..4895800 26863196 MeRIP-seq:(Medium) rs748575687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48532,Human_RBP_ID_899185,Human_RBP_ID_3951686,Human_RBP_ID_9377388,Human_RBP_ID_13064290,Human_RBP_ID_18987691,Human_RBP_ID_27812201 Human_Splice_Rec_1764772,Human_Splice_Rec_1764773,Human_Splice_Rec_1764832,Human_Splice_Rec_1764833,Human_Splice_Rec_1764894,Human_Splice_Rec_1764895,Human_Splice_Rec_1764956,Human_Splice_Rec_1764957,Human_Splice_Rec_1765018,Human_Splice_Rec_1765019,Human_Splice_Rec_1765116,Human_Splice_Rec_1765117,Human_Splice_Rec_1765146 Human_miRNA_ID_1540748,Human_miRNA_ID_1594387,Human_miRNA_ID_2938952,Human_miRNA_ID_2938953 RMVar_hsa_circ_98539,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_4642,RMVar_hsa_circ_181529,RMVar_hsa_circ_20709 104104 RMVar_ID_104104 Human_SNP_ID_615719520 m1A Human chr17 - 4895759 4895759 4895759 GTCCAGCCCTGCTTCTTCTCCACTTCTGGGTCATTGTGCAGAATCTTGTTCCGGAGCCAGGACAG GTCCAGCCCTGCTTCTTCTCCACTTCTGGGTCGTTGTGCAGAATCTTGTTCCGGAGCCAGGACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4895709..4895859 32194978 MeRIP-seq:(Medium) rs1282541914 Functional Loss SNV dbSNP153 33..33 33 - - - 104105 RMVar_ID_104105 Human_SNP_ID_615719651 m1A Human chr17 - 4896023 4896023 4896023 CTCCACGGAGCTCTTGAGGGCGATGACCAGGAACTTAATCCGCTCGTATTTCACTGGGGGCGGGA CTCCACGGAGCTCTTGAGGGCGATGACCAGGACCTTAATCCGCTCGTATTTCACTGGGGGCGGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4896003..4896113 26863196 MeRIP-seq:(Medium) rs781687108 Functional Loss SNV dbSNP153 33..33 33 - - - 104106 RMVar_ID_104106 Human_SNP_ID_615720643 m1A Human chr17 + 4897862 4897862 4897862 CCCCGCCAGCCAAAACATTCCCCCCATTCCCGACCCCCCTCTCCTCTTCTAGCCCATGCCCTTCC CCCCGCCAGCCAAAACATTCCCCCCATTCCCGCCCCCCCTCTCCTCTTCTAGCCCATGCCCTTCC A C MINK1 Ensembl:ENSG00000141503 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:4897812..4897971;chr17:4897816..4897969 26863196 MeRIP-seq:(Medium) rs1467662772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129025,Human_RBP_ID_17079431,Human_RBP_ID_18941232 Human_miRNA_ID_846561,Human_miRNA_ID_1061826,Human_miRNA_ID_1339654,Human_miRNA_ID_1385206 104107 RMVar_ID_104107 Human_SNP_ID_615720682 m1A Human chr17 + 4897924 4897920 4897924 TCCCCGGTGGAGGGAGGGAGCAGGGAGCCCTCACTCTCCACGCCCCTTGCTTGCATCTGTATATA TCCCCGGTGGAGGGAGGGAGCAGGGAGCC____CTCTCCACGCCCCTTGCTTGCATCTGTATATA CCTCA C MINK1 Ensembl:ENSG00000141503 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4897873..4897973 32194978 MeRIP-seq:(Medium) rs529707167 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_493097,Human_RBP_ID_5115023,Human_RBP_ID_5129025,Human_RBP_ID_5143076,Human_RBP_ID_5318208,Human_RBP_ID_17079431,Human_RBP_ID_18941232,Human_RBP_ID_21889889 Human_miRNA_ID_189776,Human_miRNA_ID_1339655 104108 RMVar_ID_104108 Human_SNP_ID_615720686 m1A Human chr17 + 4897924 4897924 4897924 TCCCCGGTGGAGGGAGGGAGCAGGGAGCCCTCACTCTCCACGCCCCTTGCTTGCATCTGTATATA TCCCCGGTGGAGGGAGGGAGCAGGGAGCCCTCCCTCTCCACGCCCCTTGCTTGCATCTGTATATA A C MINK1 Ensembl:ENSG00000141503 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4897873..4897973 32194978 MeRIP-seq:(Medium) rs1371585584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493097,Human_RBP_ID_5115023,Human_RBP_ID_5129025,Human_RBP_ID_5143076,Human_RBP_ID_5318208,Human_RBP_ID_17079431,Human_RBP_ID_18941232,Human_RBP_ID_21889889 Human_miRNA_ID_189776,Human_miRNA_ID_1339655 104109 RMVar_ID_104109 Human_SNP_ID_615720687 m1A Human chr17 + 4897924 4897924 4897924 TCCCCGGTGGAGGGAGGGAGCAGGGAGCCCTCACTCTCCACGCCCCTTGCTTGCATCTGTATATA TCCCCGGTGGAGGGAGGGAGCAGGGAGCCCTCTCTCTCCACGCCCCTTGCTTGCATCTGTATATA A T MINK1 Ensembl:ENSG00000141503 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:4897873..4897973 32194978 MeRIP-seq:(Medium) rs1371585584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493097,Human_RBP_ID_5115023,Human_RBP_ID_5129025,Human_RBP_ID_5143076,Human_RBP_ID_5318208,Human_RBP_ID_17079431,Human_RBP_ID_18941232,Human_RBP_ID_21889889 Human_miRNA_ID_189776,Human_miRNA_ID_1339655 104110 RMVar_ID_104110 Human_SNP_ID_615732448 m1A Human chr17 - 4933744 4933744 4933744 GGCTCTGAGGTGGTCGGGCTTGGGGTTGGTTCAGTAGTGGATTTTGGAGTTTTGGAGAATGTGAT GGCTCTGAGGTGGTCGGGCTTGGGGTTGGTTCGGTAGTGGATTTTGGAGTTTTGGAGAATGTGAT T C CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4933737..4933863 26863196 MeRIP-seq:(Medium) rs754397847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6610799,Human_RBP_ID_13064794 104111 RMVar_ID_104111 Human_SNP_ID_615734649 m1A Human chr17 + 4939976 4939976 4939976 GCGCGCGCGGCCCCGCTCGCGCCCAAGGTGACACCGCGCGCGCAACAGAGCGAGGGCGCGCGCAC GCGCGCGCGGCCCCGCTCGCGCCCAAGGTGACGCCGCGCGCGCAACAGAGCGAGGGCGCGCGCAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr17:4939885..4940004;chr17:4939904..4940004 26863410 MeRIP-seq:(Medium) rs1016379634 Functional Loss SNV dbSNP153 33..33 33 - - - 104112 RMVar_ID_104112 Human_SNP_ID_615734716 m1A Human chr17 + 4940152 4940139 4940152 GTGCGAGAAGGGGCGTAACTGATTTGGAAACCAGAGGAAAGGCGCTGTTTTCACCGAATTAGAAT GTGCGAGAAGGGGCGTAACT_____________GAGGAAAGGCGCTGTTTTCACCGAATTAGAAT TGATTTGGAAACCA T RNF167 Ensembl:ENSG00000108523 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4940101..4940375 26863196 MeRIP-seq:(Medium) rs894901724 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_1862149,Human_RBP_ID_4437426 Human_Splice_Rec_1765283,Human_Splice_Rec_1765303,Human_Splice_Rec_1765305,Human_Splice_Rec_1765319 104113 RMVar_ID_104113 Human_SNP_ID_615734722 m1A Human chr17 + 4940152 4940152 4940152 GTGCGAGAAGGGGCGTAACTGATTTGGAAACCAGAGGAAAGGCGCTGTTTTCACCGAATTAGAAT GTGCGAGAAGGGGCGTAACTGATTTGGAAACCCGAGGAAAGGCGCTGTTTTCACCGAATTAGAAT A C RNF167 Ensembl:ENSG00000108523 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4940101..4940375 26863196 MeRIP-seq:(Medium) rs896720586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1862149,Human_RBP_ID_4437426 Human_Splice_Rec_1765283,Human_Splice_Rec_1765303,Human_Splice_Rec_1765305,Human_Splice_Rec_1765319 104114 RMVar_ID_104114 Human_SNP_ID_615734899 m1A Human chr17 - 4940672 4940672 4940672 AGGCACTAAATGTATCCTTTTCTGGTACGGGGATAAAACGCGGAAAGGGGACGGAGCCTAACACA AGGCACTAAATGTATCCTTTTCTGGTACGGGGCTAAAACGCGGAAAGGGGACGGAGCCTAACACA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr17:4940501..4940925;chr17:4940570..4940709 26863196,26863410 MeRIP-seq:(Medium) rs1567654711 Functional Loss SNV dbSNP153 33..33 33 - - - 104115 RMVar_ID_104115 Human_SNP_ID_615734907 m1A Human chr17 + 4940686 4940686 4940686 TCCCCTTTCCGCGTTTTATCCCCGTACCAGAAAAGGATACATTTAGTGCCTCCCACCCAGCTCCA TCCCCTTTCCGCGTTTTATCCCCGTACCAGAAGAGGATACATTTAGTGCCTCCCACCCAGCTCCA A G RNF167 Ensembl:ENSG00000108523 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:4940585..4940725 26863196 MeRIP-seq:(Medium) rs1034181067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3527759,Human_RBP_ID_5467351,Human_RBP_ID_9377392 Human_Splice_Rec_1765285,Human_Splice_Rec_1765379 RMVar_hsa_circ_25330,RMVar_hsa_circ_181541,RMVar_hsa_circ_98162,RMVar_hsa_circ_126141,RMVar_hsa_circ_181542 104116 RMVar_ID_104116 Human_SNP_ID_615736345 m1A Human chr17 - 4944703 4944701 4944703 CCACGCAGCGGCTGTGGTAGGCTGCAGAGAGGAACAAGGTGAAGCACCTGGTGGCTGCTGGTGGC CCACGCAGCGGCTGTGGTAGGCTGCAGAGAGG__CAAGGTGAAGCACCTGGTGGCTGCTGGTGGC GTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4944701..4944725 26863196 MeRIP-seq:(Medium) rs1567662225 Functional Loss DEL dbSNP153 33..34 33 - - - 104117 RMVar_ID_104117 Human_SNP_ID_615736448 m1A Human chr17 - 4944956 4944956 4944956 GGGGACAGTGGGGGATCTGTTGAAGGCCCAGGAAAAACAAGGGGAGCTGGGGCTAAGGAACCAAA GGGGACAGTGGGGGATCTGTTGAAGGCCCAGGGAAAACAAGGGGAGCTGGGGCTAAGGAACCAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4944906..4945060 26863196 MeRIP-seq:(Medium) rs11548907 Functional Loss SNV dbSNP153 33..33 33 - - - 104118 RMVar_ID_104118 Human_SNP_ID_615736468 m1A Human chr17 - 4944982 4944982 4944982 AGACCAGGATAACAGGGGAAGAGGGAGGGGACAGTGGGGGATCTGTTGAAGGCCCAGGAAAAACA AGACCAGGATAACAGGGGAAGAGGGAGGGGACGGTGGGGGATCTGTTGAAGGCCCAGGAAAAACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4944932..4945071 26863196 MeRIP-seq:(Medium) rs1395935097 Functional Loss SNV dbSNP153 33..33 33 - - - 104119 RMVar_ID_104119 Human_SNP_ID_615736552 m1A Human chr17 + 4945155 4945155 4945155 CACACCTATCCTTTTGAGGGGCTTTGGGGTGGAGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT CACACCTATCCTTTTGAGGGGCTTTGGGGTGGCGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT A C RNF167 Ensembl:ENSG00000108523 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs6559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493341,Human_RBP_ID_822314,Human_RBP_ID_1009088,Human_RBP_ID_5115336,Human_RBP_ID_6611354,Human_RBP_ID_8819593,Human_RBP_ID_17895688,Human_RBP_ID_18941236,Human_RBP_ID_22499821,Human_RBP_ID_22805498 Human_miRNA_ID_2210755,Human_miRNA_ID_2956311 GWAS_ID_13456,GWAS_ID_13457,GWAS_ID_13458,GWAS_ID_13459,GWAS_ID_13460 RMVar_hsa_circ_181541,RMVar_hsa_circ_98162,RMVar_hsa_circ_126141,RMVar_hsa_circ_77277,RMVar_hsa_circ_181542,RMVar_hsa_circ_122770,RMVar_hsa_circ_181543,RMVar_hsa_circ_81003,RMVar_hsa_circ_112728,RMVar_hsa_circ_181544,RMVar_hsa_circ_75912,RMVar_hsa_circ_181545,RMVar_hsa_circ_181546,RMVar_hsa_circ_96484,RMVar_hsa_circ_181547,RMVar_hsa_circ_181550 104120 RMVar_ID_104120 Human_SNP_ID_615736553 m1A Human chr17 + 4945155 4945155 4945155 CACACCTATCCTTTTGAGGGGCTTTGGGGTGGAGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT CACACCTATCCTTTTGAGGGGCTTTGGGGTGGGGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT A G RNF167 Ensembl:ENSG00000108523 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs6559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493341,Human_RBP_ID_822314,Human_RBP_ID_1009088,Human_RBP_ID_5115336,Human_RBP_ID_6611354,Human_RBP_ID_8819593,Human_RBP_ID_17895688,Human_RBP_ID_18941236,Human_RBP_ID_22499821,Human_RBP_ID_22805498 Human_miRNA_ID_2210755,Human_miRNA_ID_2956311 GWAS_ID_13456,GWAS_ID_13457,GWAS_ID_13458,GWAS_ID_13459,GWAS_ID_13460 RMVar_hsa_circ_181541,RMVar_hsa_circ_98162,RMVar_hsa_circ_126141,RMVar_hsa_circ_77277,RMVar_hsa_circ_181542,RMVar_hsa_circ_122770,RMVar_hsa_circ_181543,RMVar_hsa_circ_81003,RMVar_hsa_circ_112728,RMVar_hsa_circ_181544,RMVar_hsa_circ_75912,RMVar_hsa_circ_181545,RMVar_hsa_circ_181546,RMVar_hsa_circ_96484,RMVar_hsa_circ_181547,RMVar_hsa_circ_181550 104121 RMVar_ID_104121 Human_SNP_ID_615736829 m1A Human chr17 + 4945816 4945816 4945816 TGGCAGCAATAAGGGGTATGGGGTAATGGCCCAAAAAATAAAATGGTTTGTGTGTGTATGGGGAG TGGCAGCAATAAGGGGTATGGGGTAATGGCCCCAAAAATAAAATGGTTTGTGTGTGTATGGGGAG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4945727..4945971 26863196 MeRIP-seq:(Medium) rs945915055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8456449 104122 RMVar_ID_104122 Human_SNP_ID_615736875 m1A Human chr17 + 4945894 4945894 4945894 AGCTGTGGGGAGCGGTGAAGGGGAAGGGACAGACGAGGTCAGTACTGGGAACGCCGAAGGTGGGA AGCTGTGGGGAGCGGTGAAGGGGAAGGGACAGGCGAGGTCAGTACTGGGAACGCCGAAGGTGGGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:4945726..4946748 26863410 MeRIP-seq:(Medium) rs1345779550 Functional Loss SNV dbSNP153 33..33 33 - - - 104123 RMVar_ID_104123 Human_SNP_ID_615737237 m1A Human chr17 + 4946828 4946828 4946828 CAACCAGGACACCCACCTCAGCTGGCTGGAAGAGGAACCAAGCGCCCATCAAGTTAGTCAGTGCA CAACCAGGACACCCACCTCAGCTGGCTGGAAGCGGAACCAAGCGCCCATCAAGTTAGTCAGTGCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:4946826..4946850 26863196 MeRIP-seq:(Medium) rs1038366120 Functional Loss SNV dbSNP153 33..33 33 - - - 104124 RMVar_ID_104124 Human_SNP_ID_615737881 m1A Human chr17 - 4948381 4948381 4948381 CAGCCCCAGTAGCAGCGCCATGGCCGGGTGGAACGCCTACATCGACAACCTCATGGCGGACGGGA CAGCCCCAGTAGCAGCGCCATGGCCGGGTGGACCGCCTACATCGACAACCTCATGGCGGACGGGA T G PFN1 Ensembl:ENSG00000108518 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr17:4948188..4948575;chr17:4948076..4949244 26863196 MeRIP-seq:(Medium) rs1194625099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50419,Human_RBP_ID_235852,Human_RBP_ID_493365,Human_RBP_ID_904372,Human_RBP_ID_1009103,Human_RBP_ID_1287361,Human_RBP_ID_1536903,Human_RBP_ID_1862248,Human_RBP_ID_3527854,Human_RBP_ID_4464259,Human_RBP_ID_5318846,Human_RBP_ID_6611411,Human_RBP_ID_8456467,Human_RBP_ID_8819602,Human_RBP_ID_13066508,Human_RBP_ID_17260677,Human_RBP_ID_17654489,Human_RBP_ID_17692465,Human_RBP_ID_18702008,Human_RBP_ID_22443364,Human_RBP_ID_24479633,Human_RBP_ID_26811850,Human_RBP_ID_26965865,Human_RBP_ID_27156643,Human_RBP_ID_27256666 RMVar_hsa_circ_113807,RMVar_hsa_circ_82803,RMVar_hsa_circ_181553,RMVar_hsa_circ_181555 104125 RMVar_ID_104125 Human_SNP_ID_615737885 m1A Human chr17 - 4948417 4948394 4948418 GAGCCCAGTCCGCGGCCCCAGCAGCAGCGCCGAGAGCAGCCCCAGTAGCAGCGCCATGGCCGGGT GAGCCCAGTCCGCGGCCCCAGCAGCAGCGCC________________________ATGGCCGGGT TGGCGCTGCTACTGGGGCTGCTCTC T PFN1 Ensembl:ENSG00000108518 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr17:4948081..4950293;chr17:4948263..4948564;chr17:4948367..4948525 26863196 MeRIP-seq:(Medium) rs1175151136 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_50419,Human_RBP_ID_235852,Human_RBP_ID_493365,Human_RBP_ID_904372,Human_RBP_ID_1536904,Human_RBP_ID_1862248,Human_RBP_ID_4464259,Human_RBP_ID_5318846,Human_RBP_ID_9327145,Human_RBP_ID_20234059,Human_RBP_ID_22443365,Human_RBP_ID_24479634,Human_RBP_ID_26811851,Human_RBP_ID_26965865 Human_miRNA_ID_2017978 RMVar_hsa_circ_113807,RMVar_hsa_circ_82803,RMVar_hsa_circ_181553,RMVar_hsa_circ_181555 104126 RMVar_ID_104126 Human_SNP_ID_615737888 m1A Human chr17 - 4948400 4948400 4948400 CCAGCAGCAGCGCCGAGAGCAGCCCCAGTAGCAGCGCCATGGCCGGGTGGAACGCCTACATCGAC CCAGCAGCAGCGCCGAGAGCAGCCCCAGTAGCGGCGCCATGGCCGGGTGGAACGCCTACATCGAC T C PFN1 Ensembl:ENSG00000108518 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:4948178..4949244 26863196 MeRIP-seq:(Medium) rs374939304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50419,Human_RBP_ID_235852,Human_RBP_ID_493365,Human_RBP_ID_904372,Human_RBP_ID_1287361,Human_RBP_ID_1536903,Human_RBP_ID_1862248,Human_RBP_ID_4464259,Human_RBP_ID_5318846,Human_RBP_ID_6611411,Human_RBP_ID_9327145,Human_RBP_ID_17654489,Human_RBP_ID_17692465,Human_RBP_ID_18702008,Human_RBP_ID_22443365,Human_RBP_ID_22805505,Human_RBP_ID_24415479,Human_RBP_ID_24479634,Human_RBP_ID_26811850,Human_RBP_ID_26965865,Human_RBP_ID_27256666 Human_miRNA_ID_2975797,Human_miRNA_ID_3115220 RMVar_hsa_circ_113807,RMVar_hsa_circ_82803,RMVar_hsa_circ_181553,RMVar_hsa_circ_181555 104127 RMVar_ID_104127 Human_SNP_ID_615737926 m1A Human chr17 - 4948458 4948458 4948458 CGAGCTCTCCGCCTCCCCCCGCCCGCCAGCCGAGGCAGCTCGAGCCCAGTCCGCGGCCCCAGCAG CGAGCTCTCCGCCTCCCCCCGCCCGCCAGCCGTGGCAGCTCGAGCCCAGTCCGCGGCCCCAGCAG T A PFN1 Ensembl:ENSG00000108518 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr17:4948337..4948575;chr17:4948380..4948550 26863410 MeRIP-seq:(Medium) rs1372261988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50419,Human_RBP_ID_235852,Human_RBP_ID_493367,Human_RBP_ID_764721,Human_RBP_ID_904372,Human_RBP_ID_4437779,Human_RBP_ID_5318846,Human_RBP_ID_8253517,Human_RBP_ID_9073346,Human_RBP_ID_9326434,Human_RBP_ID_13234389,Human_RBP_ID_18702012,Human_RBP_ID_22443365,Human_RBP_ID_22532944,Human_RBP_ID_24415480,Human_RBP_ID_24479638,Human_RBP_ID_26811851,Human_RBP_ID_26965867,Human_RBP_ID_27256667,Human_RBP_ID_27454367 Human_Splice_Rec_1765448 Human_miRNA_ID_2242106,Human_miRNA_ID_2554784 RMVar_hsa_circ_113807,RMVar_hsa_circ_82803,RMVar_hsa_circ_181553,RMVar_hsa_circ_181555 104128 RMVar_ID_104128 Human_SNP_ID_615737982 m1A Human chr17 + 4948511 4948507 4948511 GCGGAGAGCTCGGGGCACGCGCTGCCGTCCGGACCGCGGCTCCGCTCGCTGTGCAGCAGCCCTCG GCGGAGAGCTCGGGGCACGCGCTGCCGTC____CCGCGGCTCCGCTCGCTGTGCAGCAGCCCTCG CCGGA C ENO3 Ensembl:ENSG00000108515 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:4948415..4948515 26863410 MeRIP-seq:(Medium) rs756255421 Functional Loss DEL dbSNP153 30..33 33 - - - 104129 RMVar_ID_104129 Human_SNP_ID_615738180 m1A Human chr17 - 4948929 4948929 4948929 TCCTTCCCTTCGGCGGAGGTGGGGGAAGGAGGAGTCATCCCGTTTAACCCTGGGCTCCCCGAACT TCCTTCCCTTCGGCGGAGGTGGGGGAAGGAGGCGTCATCCCGTTTAACCCTGGGCTCCCCGAACT T G PFN1 Ensembl:ENSG00000108518 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:4948837..4948928 26863410 MeRIP-seq:(Medium) rs1165011151 Functional Loss SNV dbSNP153 33..33 33 - - - 104130 RMVar_ID_104130 Human_SNP_ID_615738656 m1A Human chr17 - 4950176 4950176 4950176 CCTCTGCAGCCATACCAGCCGACCGGCGGGGGACACACGGCGCCTCGGCCCGACTCGGAGGCCCT CCTCTGCAGCCATACCAGCCGACCGGCGGGGGGCACACGGCGCCTCGGCCCGACTCGGAGGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4950149..4950216 26863196 MeRIP-seq:(Medium) rs1479762928 Functional Loss SNV dbSNP153 33..33 33 - - - 104131 RMVar_ID_104131 Human_SNP_ID_615738935 m1A Human chr17 + 4951031 4951031 4951031 GTAGTGGGCACTTGGCTGCCAGCCCAGTGTGAAGGGGGGAGGATGGAGAGAAAGAGAGGCGGGGC GTAGTGGGCACTTGGCTGCCAGCCCAGTGTGACGGGGGGAGGATGGAGAGAAAGAGAGGCGGGGC A C ENO3 Ensembl:ENSG00000108515 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4950995..4951121 26863196 MeRIP-seq:(Medium) rs1471353931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17068161 104132 RMVar_ID_104132 Human_SNP_ID_615738977 m1A Human chr17 + 4951167 4951167 4951167 CCACCTAGACTCGGAGCTCCATCCAAACCTCCAGCGAAGACATCCCAGGTCGGGTGAATCTTCCA CCACCTAGACTCGGAGCTCCATCCAAACCTCCGGCGAAGACATCCCAGGTCGGGTGAATCTTCCA A G ENO3 Ensembl:ENSG00000108515 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4950958..4951627 26863196 MeRIP-seq:(Medium) rs1271335854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764709 Human_Splice_Rec_1765481,Human_Splice_Rec_1765489,Human_Splice_Rec_1765509,Human_Splice_Rec_1765511,Human_Splice_Rec_1765515,Human_Splice_Rec_1765523,Human_Splice_Rec_1765533,Human_Splice_Rec_1765547,Human_Splice_Rec_1765565,Human_Splice_Rec_1765585 RMVar_hsa_circ_106287,RMVar_hsa_circ_181556 104133 RMVar_ID_104133 Human_SNP_ID_615739787 m1A Human chr17 - 4953343 4953343 4953343 CTCATCCCTTCCCCACCGCTAGCCCTTCACTCACACTTATTCTCGGTCCCATCTAGCTCAATCAT CTCATCCCTTCCCCACCGCTAGCCCTTCACTCCCACTTATTCTCGGTCCCATCTAGCTCAATCAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4953248..4953365 26863196 MeRIP-seq:(Medium) rs780926849 Functional Loss SNV dbSNP153 33..33 33 - - - 104134 RMVar_ID_104134 Human_SNP_ID_615740399 m1A Human chr17 - 4955182 4955182 4955182 ACCCCCTTGAGGTGGTGGTAGACCTCGGCGCCAATGCGCATGGCTTCCTTGAAGGAGCTGGCTCC ACCCCCTTGAGGTGGTGGTAGACCTCGGCGCCGATGCGCATGGCTTCCTTGAAGGAGCTGGCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4955138..4955240 26863196 MeRIP-seq:(Medium) rs1251442649 Functional Loss SNV dbSNP153 33..33 33 - - - 104135 RMVar_ID_104135 Human_SNP_ID_615741043 m1A Human chr17 + 4956638 4956638 4956638 GATGGTGAGCCACCGCTCTGGGGAGACTGAGGACACATTCATTGCTGACCTTGTGGTGGGGCTCT GATGGTGAGCCACCGCTCTGGGGAGACTGAGGCCACATTCATTGCTGACCTTGTGGTGGGGCTCT A C ENO3 Ensembl:ENSG00000108515 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4956554..4956703 26863196 MeRIP-seq:(Medium) rs766870438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18164587,Human_RBP_ID_18987709,Human_RBP_ID_27454390 Human_Splice_Rec_1765504,Human_Splice_Rec_1765505,Human_Splice_Rec_1765560,Human_Splice_Rec_1765561,Human_Splice_Rec_1765580,Human_Splice_Rec_1765581,Human_Splice_Rec_1765600,Human_Splice_Rec_1765601,Human_Splice_Rec_1765606,Human_Splice_Rec_1765607,Human_Splice_Rec_1765611 RMVar_hsa_circ_105693,RMVar_hsa_circ_181567 104136 RMVar_ID_104136 Human_SNP_ID_615741963 m1A Human chr17 + 4959407 4959407 4959407 AACGGTGACAAATCAAACACCTGTTTTCCCCCAGCCTGAGGGACAGCTGGTAGGAGGTGGTTCAG AACGGTGACAAATCAAACACCTGTTTTCCCCCCGCCTGAGGGACAGCTGGTAGGAGGTGGTTCAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4959356..4959534 26863196 MeRIP-seq:(Medium) rs1393944640 Functional Loss SNV dbSNP153 33..33 33 - - - 104137 RMVar_ID_104137 Human_SNP_ID_615742201 m1A Human chr17 + 4959912 4959912 4959912 GCTGGGCTGCCTCCTCCTCTTGCCTCTGGGCCAGCTCCTAGGGGTGAAAGTGGGGGCACTGGTGC GCTGGGCTGCCTCCTCCTCTTGCCTCTGGGCCGGCTCCTAGGGGTGAAAGTGGGGGCACTGGTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:4959750..4959913;chr17:4959751..4960137 26863196,32194978 MeRIP-seq:(Medium) rs1287569101 Functional Loss SNV dbSNP153 33..33 33 - - - 104138 RMVar_ID_104138 Human_SNP_ID_615744625 m1A Human chr17 - 4967699 4967699 4967699 GCAAGGCCCGAGGTGAGGATCCCAAATTCACAACCGCCTTCCTTCGCCCGGTTCTCGGGACCATA GCAAGGCCCGAGGTGAGGATCCCAAATTCACAGCCGCCTTCCTTCGCCCGGTTCTCGGGACCATA T C SPAG7 Ensembl:ENSG00000091640 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4967693..4967766 26863196 MeRIP-seq:(Medium) rs746946989 Functional Loss SNV dbSNP153 33..33 33 - - - 104139 RMVar_ID_104139 Human_SNP_ID_615744666 m1A Human chr17 + 4967770 4967770 4967770 TCTCCTGGTCACCGAGGCTGGGTGGCTTCTCCATGGAGCTCAGGATGGAGCCCAGTAGGTCCGCC TCTCCTGGTCACCGAGGCTGGGTGGCTTCTCCTTGGAGCTCAGGATGGAGCCCAGTAGGTCCGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4967613..4967825 26863196 MeRIP-seq:(Medium) rs781027670 Functional Loss SNV dbSNP153 33..33 33 - - - 104140 RMVar_ID_104140 Human_SNP_ID_615744679 m1A Human chr17 + 4967786 4967786 4967786 GCTGGGTGGCTTCTCCATGGAGCTCAGGATGGAGCCCAGTAGGTCCGCCATCTTGGGAGTGACTG GCTGGGTGGCTTCTCCATGGAGCTCAGGATGGCGCCCAGTAGGTCCGCCATCTTGGGAGTGACTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4967776..4967800 26863196 MeRIP-seq:(Medium) rs1294787221 Functional Loss SNV dbSNP153 33..33 33 - - - 104141 RMVar_ID_104141 Human_SNP_ID_615744914 m1A Human chr17 + 4968480 4968480 4968480 GAGTCGGGTGCAGGCAGGAGGAGCTGGGGAGCAGGGGCAGGCAGGGCTCCGGAGGTCACAGCGGA GAGTCGGGTGCAGGCAGGAGGAGCTGGGGAGCGGGGGCAGGCAGGGCTCCGGAGGTCACAGCGGA A G AC004771.3 Ensembl:ENSG00000262429 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4968058..4968675 26863196 MeRIP-seq:(Medium) rs1225240824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901472,Human_RBP_ID_3549053,Human_RBP_ID_5188807,Human_RBP_ID_8193816,Human_RBP_ID_26781927 104142 RMVar_ID_104142 Human_SNP_ID_615745200 m1A Human chr17 - 4969242 4969242 4969242 TATGAACAGAAGCGATTTCAGCAGAGCCGCCGAGCGGCTGTGCTCATCCAGCAGCACTACCGCTC TATGAACAGAAGCGATTTCAGCAGAGCCGCCGGGCGGCTGTGCTCATCCAGCAGCACTACCGCTC T C CAMTA2 Ensembl:ENSG00000108509 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4969028..4969267 26863196 MeRIP-seq:(Medium) rs1324237798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237624,Human_RBP_ID_493449,Human_RBP_ID_18990192 Human_Splice_Rec_1765704,Human_Splice_Rec_1765705,Human_Splice_Rec_1765748,Human_Splice_Rec_1765749,Human_Splice_Rec_1765790,Human_Splice_Rec_1765791,Human_Splice_Rec_1765834,Human_Splice_Rec_1765835,Human_Splice_Rec_1765874,Human_Splice_Rec_1765875,Human_Splice_Rec_1765918,Human_Splice_Rec_1765919,Human_Splice_Rec_1765925 Human_miRNA_ID_172245 RMVar_hsa_circ_68563,RMVar_hsa_circ_50846 104143 RMVar_ID_104143 Human_SNP_ID_615745591 m1A Human chr17 + 4970372 4970372 4970372 CTGGGAGGGGTTGAGCTGGGGAAATGGTCCACATTCTCCAGGTAGCTGGCCAGCCAGGACATGGT CTGGGAGGGGTTGAGCTGGGGAAATGGTCCACGTTCTCCAGGTAGCTGGCCAGCCAGGACATGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4970370..4970485 26863196 MeRIP-seq:(Medium) rs769089277 Functional Loss SNV dbSNP153 33..33 33 - - - 104144 RMVar_ID_104144 Human_SNP_ID_615745592 m1A Human chr17 + 4970372 4970372 4970372 CTGGGAGGGGTTGAGCTGGGGAAATGGTCCACATTCTCCAGGTAGCTGGCCAGCCAGGACATGGT CTGGGAGGGGTTGAGCTGGGGAAATGGTCCACTTTCTCCAGGTAGCTGGCCAGCCAGGACATGGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4970370..4970485 26863196 MeRIP-seq:(Medium) rs769089277 Functional Loss SNV dbSNP153 33..33 33 - - - 104145 RMVar_ID_104145 Human_SNP_ID_615748391 m1A Human chr17 + 4979793 4979793 4979793 TGCTTGGAGCTTCGTCACTGATGAGTTCTCCCATAAGGTCTGGGAATGATGAAAGACTGAAGGGC TGCTTGGAGCTTCGTCACTGATGAGTTCTCCCCTAAGGTCTGGGAATGATGAAAGACTGAAGGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4974430..4980386 32194978 MeRIP-seq:(Medium) rs377223149 Functional Loss SNV dbSNP153 33..33 33 - - - 104146 RMVar_ID_104146 Human_SNP_ID_615748392 m1A Human chr17 + 4979793 4979793 4979793 TGCTTGGAGCTTCGTCACTGATGAGTTCTCCCATAAGGTCTGGGAATGATGAAAGACTGAAGGGC TGCTTGGAGCTTCGTCACTGATGAGTTCTCCCGTAAGGTCTGGGAATGATGAAAGACTGAAGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4974430..4980386 32194978 MeRIP-seq:(Medium) rs377223149 Functional Loss SNV dbSNP153 33..33 33 - - - 104147 RMVar_ID_104147 Human_SNP_ID_615748668 m1A Human chr17 - 4980479 4980479 4980479 GAGCCTCCTCCACTGATAGCCCCACTTCCCCCAGAGCTCCCCAAGGCACACACCTCCCCATCTTC GAGCCTCCTCCACTGATAGCCCCACTTCCCCCCGAGCTCCCCAAGGCACACACCTCCCCATCTTC T G CAMTA2 Ensembl:ENSG00000108509 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4980431..4980596 26863196 MeRIP-seq:(Medium) rs1178775731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17079434,Human_RBP_ID_18941249 RMVar_hsa_circ_120129,RMVar_hsa_circ_181571,RMVar_hsa_circ_87430,RMVar_hsa_circ_181572 104148 RMVar_ID_104148 Human_SNP_ID_615748711 m1A Human chr17 + 4980569 4980569 4980569 GTCAGGGTTAAAGCTCGGGGCTCCACTTTGGGAGAGATGATGCGGTGTTTCGTGCTGCTGCATTT GTCAGGGTTAAAGCTCGGGGCTCCACTTTGGGGGAGATGATGCGGTGTTTCGTGCTGCTGCATTT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4980391..4980581 26863196 MeRIP-seq:(Medium) rs574836036 Functional Loss SNV dbSNP153 33..33 33 - - - 104149 RMVar_ID_104149 Human_SNP_ID_615750295 m1A Human chr17 + 4986260 4986236 4986260 GGGCTCCAGGGGGCAAGGTCACCCCCGGCCTGAGGGGCCGGGGGGAGGGGGAGTCTGTGCTGGGA GGGCTCCAG________________________GGGGCCGGGGGGAGGGGGAGTCTGTGCTGGGA GGGGGCAAGGTCACCCCCGGCCTGA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4986176..4986325 26863410 MeRIP-seq:(Medium) rs776549366 Functional Loss DEL dbSNP153 10..33 33 - - - 104150 RMVar_ID_104150 Human_SNP_ID_615750321 m1A Human chr17 + 4986260 4986260 4986260 GGGCTCCAGGGGGCAAGGTCACCCCCGGCCTGAGGGGCCGGGGGGAGGGGGAGTCTGTGCTGGGA GGGCTCCAGGGGGCAAGGTCACCCCCGGCCTGGGGGGCCGGGGGGAGGGGGAGTCTGTGCTGGGA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4986176..4986325 26863410 MeRIP-seq:(Medium) rs780459932 Functional Loss SNV dbSNP153 33..33 33 - - - 104151 RMVar_ID_104151 Human_SNP_ID_615750830 m1A Human chr17 + 4987733 4987733 4987733 CTCCCAATTAAGGGGATGAGGGTCAGGAAGGGAACCTGGGGTCAGCACACGTGGAGTTCTGGGTG CTCCCAATTAAGGGGATGAGGGTCAGGAAGGGCACCTGGGGTCAGCACACGTGGAGTTCTGGGTG A C AC004771.2 Ensembl:ENSG00000262227 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4987726..4987935 26863196 MeRIP-seq:(Medium) rs1285413035 Functional Loss SNV dbSNP153 33..33 33 - - - 104152 RMVar_ID_104152 Human_SNP_ID_615754082 m1A Human chr17 + 4998045 4998045 4998045 GAGTCCGCCGCCCGCCGCCCGGGCACCCGGCGAGGGGCGGGGGCAGCTCCGAACCGGCCCCAGAT GAGTCCGCCGCCCGCCGCCCGGGCACCCGGCGGGGGGCGGGGGCAGCTCCGAACCGGCCCCAGAT A G KIF1C Ensembl:ENSG00000129250 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:4997951..4998175 26863410 MeRIP-seq:(Medium) rs377662236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464260,Human_RBP_ID_8824339,Human_RBP_ID_9289733 104153 RMVar_ID_104153 Human_SNP_ID_615754088 m1A Human chr17 - 4998060 4998060 4998060 GCGGAAGCGGGAAGGATCTGGGGCCGGTTCGGAGCTGCCCCCGCCCCTCGCCGGGTGCCCGGGCG GCGGAAGCGGGAAGGATCTGGGGCCGGTTCGGGGCTGCCCCCGCCCCTCGCCGGGTGCCCGGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4997926..4999927 26863196 MeRIP-seq:(Medium) rs1296249855 Functional Loss SNV dbSNP153 33..33 33 - - - 104154 RMVar_ID_104154 Human_SNP_ID_615754097 m1A Human chr17 + 4998076 4998076 4998076 GAGGGGCGGGGGCAGCTCCGAACCGGCCCCAGATCCTTCCCGCTTCCGCCTCACGCTTCCCGGAA GAGGGGCGGGGGCAGCTCCGAACCGGCCCCAGCTCCTTCCCGCTTCCGCCTCACGCTTCCCGGAA A C KIF1C Ensembl:ENSG00000129250 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4997926..4999856 26863196 MeRIP-seq:(Medium) rs144190290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4438426,Human_RBP_ID_5466688,Human_RBP_ID_6612409 Human_Splice_Rec_1766047,Human_Splice_Rec_1766091 104155 RMVar_ID_104155 Human_SNP_ID_615754119 m1A Human chr17 + 4998109 4998109 4998109 TCCTTCCCGCTTCCGCCTCACGCTTCCCGGAAAGCTTGTCCCTCTCCGCCGAGCTGCTCCGGGAG TCCTTCCCGCTTCCGCCTCACGCTTCCCGGAAGGCTTGTCCCTCTCCGCCGAGCTGCTCCGGGAG A G KIF1C Ensembl:ENSG00000129250 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:4997951..4998228 26863196 MeRIP-seq:(Medium) rs1430933056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768438,Human_RBP_ID_4438429 Human_Splice_Rec_1766047,Human_Splice_Rec_1766091 104156 RMVar_ID_104156 Human_SNP_ID_615754817 m1A Human chr17 + 5000344 5000344 5000344 GGATGCCAAGTGTGTGGTCAGCATGCAGGGCAACACCACCTGTGAGTGAGTCCCCGGGGCCTGGC GGATGCCAAGTGTGTGGTCAGCATGCAGGGCACCACCACCTGTGAGTGAGTCCCCGGGGCCTGGC A C KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5000226..5000386 26863196 MeRIP-seq:(Medium) rs1308685223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464265,Human_RBP_ID_18702312 Human_Splice_Rec_1766051,Human_Splice_Rec_1766097 Human_miRNA_ID_3091074 RMVar_hsa_circ_80301,RMVar_hsa_circ_60505,RMVar_hsa_circ_102051,RMVar_hsa_circ_44265,RMVar_hsa_circ_181574,RMVar_hsa_circ_181575 104157 RMVar_ID_104157 Human_SNP_ID_615755581 m1A Human chr17 - 5002621 5002621 5002621 GCCTGCCTCACCGTGCTTTATTTCCACAGTCCATGAGGTCAGCAATGTCTGCGTAGGAGGTCACA GCCTGCCTCACCGTGCTTTATTTCCACAGTCCCTGAGGTCAGCAATGTCTGCGTAGGAGGTCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5002572..5002722 26863196 MeRIP-seq:(Medium) rs767276837 Functional Loss SNV dbSNP153 33..33 33 - - - 104158 RMVar_ID_104158 Human_SNP_ID_615755589 m1A Human chr17 - 5002644 5002644 5002644 CCCCCTTGCCCTCTGCTCCATCAGCCTGCCTCACCGTGCTTTATTTCCACAGTCCATGAGGTCAG CCCCCTTGCCCTCTGCTCCATCAGCCTGCCTCCCCGTGCTTTATTTCCACAGTCCATGAGGTCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:5002629..5002741 26863196 MeRIP-seq:(Medium) rs1181193435 Functional Loss SNV dbSNP153 33..33 33 - - - 104159 RMVar_ID_104159 Human_SNP_ID_615755666 m1A Human chr17 - 5002834 5002834 5002834 GAGTGGGGGGGGGGGCGATCCCACCTTCTCCGAGTCCAGCCCCGTGAGCTGGTCATGGCAGCGCT GAGTGGGGGGGGGGGCGATCCCACCTTCTCCGTGTCCAGCCCCGTGAGCTGGTCATGGCAGCGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5002784..5002875 26863196 MeRIP-seq:(Medium) rs756742766 Functional Loss SNV dbSNP153 33..33 33 - - - 104160 RMVar_ID_104160 Human_SNP_ID_615756023 m1A Human chr17 + 5003665 5003664 5003666 GACCTTGCTGGGAGTGAGCGAGCCGACTCCTCAGGGGCCCGGGGCATGCGCCTGAAGGTGAGGGG GACCTTGCTGGGAGTGAGCGAGCCGACTCCTC__GGGCCCGGGGCATGCGCCTGAAGGTGAGGGG CAG C KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5003586..5003719 26863196 MeRIP-seq:(Medium) rs1339514897 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_236121,Human_RBP_ID_765173,Human_RBP_ID_904888,Human_RBP_ID_1862597 Human_Splice_Rec_1766062,Human_Splice_Rec_1766063 RMVar_hsa_circ_60505,RMVar_hsa_circ_102051,RMVar_hsa_circ_181574,RMVar_hsa_circ_113010,RMVar_hsa_circ_78360,RMVar_hsa_circ_101843,RMVar_hsa_circ_181576,RMVar_hsa_circ_181577,RMVar_hsa_circ_181579,RMVar_hsa_circ_97430,RMVar_hsa_circ_181578,RMVar_hsa_circ_7130,RMVar_hsa_circ_79275,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_16706,RMVar_hsa_circ_181582 104161 RMVar_ID_104161 Human_SNP_ID_615756025 m1A Human chr17 + 5003665 5003665 5003665 GACCTTGCTGGGAGTGAGCGAGCCGACTCCTCAGGGGCCCGGGGCATGCGCCTGAAGGTGAGGGG GACCTTGCTGGGAGTGAGCGAGCCGACTCCTCGGGGGCCCGGGGCATGCGCCTGAAGGTGAGGGG A G KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5003586..5003719 26863196 MeRIP-seq:(Medium) rs999612430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236121,Human_RBP_ID_765173,Human_RBP_ID_904888,Human_RBP_ID_1862597 Human_Splice_Rec_1766062,Human_Splice_Rec_1766063 RMVar_hsa_circ_60505,RMVar_hsa_circ_102051,RMVar_hsa_circ_181574,RMVar_hsa_circ_113010,RMVar_hsa_circ_78360,RMVar_hsa_circ_101843,RMVar_hsa_circ_181576,RMVar_hsa_circ_181577,RMVar_hsa_circ_181579,RMVar_hsa_circ_97430,RMVar_hsa_circ_181578,RMVar_hsa_circ_7130,RMVar_hsa_circ_79275,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_16706,RMVar_hsa_circ_181582 104162 RMVar_ID_104162 Human_SNP_ID_615756026 m1A Human chr17 + 5003665 5003665 5003665 GACCTTGCTGGGAGTGAGCGAGCCGACTCCTCAGGGGCCCGGGGCATGCGCCTGAAGGTGAGGGG GACCTTGCTGGGAGTGAGCGAGCCGACTCCTCTGGGGCCCGGGGCATGCGCCTGAAGGTGAGGGG A T KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5003586..5003719 26863196 MeRIP-seq:(Medium) rs999612430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236121,Human_RBP_ID_765173,Human_RBP_ID_904888,Human_RBP_ID_1862597 Human_Splice_Rec_1766062,Human_Splice_Rec_1766063 RMVar_hsa_circ_60505,RMVar_hsa_circ_102051,RMVar_hsa_circ_181574,RMVar_hsa_circ_113010,RMVar_hsa_circ_78360,RMVar_hsa_circ_101843,RMVar_hsa_circ_181576,RMVar_hsa_circ_181577,RMVar_hsa_circ_181579,RMVar_hsa_circ_97430,RMVar_hsa_circ_181578,RMVar_hsa_circ_7130,RMVar_hsa_circ_79275,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_16706,RMVar_hsa_circ_181582 104163 RMVar_ID_104163 Human_SNP_ID_615756467 m1A Human chr17 - 5004982 5004982 5004982 CCTGGAACCTCGACCTTCCAGAGCAGAGGCTGACAGTCCCTGAGCCATCAGCAGTTCCCGCAGCC CCTGGAACCTCGACCTTCCAGAGCAGAGGCTGGCAGTCCCTGAGCCATCAGCAGTTCCCGCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5004819..5005036 26863196 MeRIP-seq:(Medium) rs867611760 Functional Loss SNV dbSNP153 33..33 33 - - - 104164 RMVar_ID_104164 Human_SNP_ID_615757119 m1A Human chr17 + 5007083 5007083 5007083 GATTGGGCCTGAGGAAGCCATGGAGAGGCTGCAGGTGGGAAGCTGGAGCTGGCAAGGGCTGGGGG GATTGGGCCTGAGGAAGCCATGGAGAGGCTGCCGGTGGGAAGCTGGAGCTGGCAAGGGCTGGGGG A C KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5006877..5007131 26863196 MeRIP-seq:(Medium) rs1448349099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821919,Human_RBP_ID_19081211,Human_RBP_ID_24372148 Human_Splice_Rec_1766073 RMVar_hsa_circ_3667,RMVar_hsa_circ_60505,RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_356994,RMVar_hsa_circ_52813,RMVar_hsa_circ_52147,RMVar_hsa_circ_181583,RMVar_hsa_circ_60269,RMVar_hsa_circ_305052 104165 RMVar_ID_104165 Human_SNP_ID_615757399 m1A Human chr17 - 5007944 5007944 5007944 TCCATCTATAACCAACCCCTCGCTGCACTGGCAACCACTGTCTTACAATGTAGTGCTCATGCCTC TCCATCTATAACCAACCCCTCGCTGCACTGGCGACCACTGTCTTACAATGTAGTGCTCATGCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5007940..5008143 26863196 MeRIP-seq:(Medium) rs79554147 Functional Loss SNV dbSNP153 33..33 33 - - - 104166 RMVar_ID_104166 Human_SNP_ID_615758710 m1A Human chr17 - 5012509 5012509 5012509 CCTGGGCCTCCTCCATGTCCCGGCTCCAGTCCATCTGTCCAAGCCCCCCTCCCAGGCTCTCTCCC CCTGGGCCTCCTCCATGTCCCGGCTCCAGTCCGTCTGTCCAAGCCCCCCTCCCAGGCTCTCTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5012503..5012739 26863196 MeRIP-seq:(Medium) rs566377254 Functional Loss SNV dbSNP153 33..33 33 - - - 104167 RMVar_ID_104167 Human_SNP_ID_615758711 m1A Human chr17 - 5012509 5012509 5012509 CCTGGGCCTCCTCCATGTCCCGGCTCCAGTCCATCTGTCCAAGCCCCCCTCCCAGGCTCTCTCCC CCTGGGCCTCCTCCATGTCCCGGCTCCAGTCCCTCTGTCCAAGCCCCCCTCCCAGGCTCTCTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5012503..5012739 26863196 MeRIP-seq:(Medium) rs566377254 Functional Loss SNV dbSNP153 33..33 33 - - - 104168 RMVar_ID_104168 Human_SNP_ID_615760775 m1A Human chr17 - 5020051 5020051 5020051 CTACCTGACTTCAGCACCAGCGGCTCCGTCACAAGCTTCCCATTCACATATGTCTCAGCTCCTTC CTACCTGACTTCAGCACCAGCGGCTCCGTCACGAGCTTCCCATTCACATATGTCTCAGCTCCTTC T C KIF1C-AS1 Ensembl:ENSG00000227495 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5020001..5020100 26863196 MeRIP-seq:(Medium) rs777346088 Functional Loss SNV dbSNP153 33..33 33 - - - 104169 RMVar_ID_104169 Human_SNP_ID_615761591 m1A Human chr17 + 5022460 5022460 5022460 TGTCGCACCTATGGCAAGCCAGACGGCCCCGGAGACGCCTGGAGGGCTGTGGCCCGGGATGTCTG TGTCGCACCTATGGCAAGCCAGACGGCCCCGGGGACGCCTGGAGGGCTGTGGCCCGGGATGTCTG A G KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:5022401..5022583 26863196 MeRIP-seq:(Medium) rs1251852388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130955,Human_RBP_ID_493797,Human_RBP_ID_3528360,Human_RBP_ID_9289743,Human_RBP_ID_17905674 RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_181583,RMVar_hsa_circ_75706,RMVar_hsa_circ_119211,RMVar_hsa_circ_181585,RMVar_hsa_circ_86680,RMVar_hsa_circ_181586,RMVar_hsa_circ_181587 104170 RMVar_ID_104170 Human_SNP_ID_615761628 m1A Human chr17 + 5022530 5022530 5022530 CTGTAGGCGAGGAGGAAGGAGGTGGAGCTGGCAGTGGTGGTGGCAGTGAGGAGGGAGCCCGAGGG CTGTAGGCGAGGAGGAAGGAGGTGGAGCTGGCTGTGGTGGTGGCAGTGAGGAGGGAGCCCGAGGG A T KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:5022076..5022725;chr17:5020587..5023626 26863196 MeRIP-seq:(Medium) rs956991329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130955,Human_RBP_ID_898215,Human_RBP_ID_4438883,Human_RBP_ID_5115344,Human_RBP_ID_8824349,Human_RBP_ID_9289744,Human_RBP_ID_17669944,Human_RBP_ID_27454544 RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_181583,RMVar_hsa_circ_75706,RMVar_hsa_circ_119211,RMVar_hsa_circ_181585,RMVar_hsa_circ_86680,RMVar_hsa_circ_181586,RMVar_hsa_circ_181587 104171 RMVar_ID_104171 Human_SNP_ID_615762129 m1A Human chr17 + 5023882 5023882 5023882 AACCCCCTGAGGAGGTCACTCCCCATCCAGCCACCCCTGCCCGCCGGCCTCCGAGTCCCCGAAGG AACCCCCTGAGGAGGTCACTCCCCATCCAGCCCCCCCTGCCCGCCGGCCTCCGAGTCCCCGAAGG A C KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:5023751..5024025 26863196 MeRIP-seq:(Medium) rs1014528756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_902896,Human_RBP_ID_17080459,Human_RBP_ID_18941256,Human_RBP_ID_27454550 RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_181583,RMVar_hsa_circ_75706,RMVar_hsa_circ_119211,RMVar_hsa_circ_181585,RMVar_hsa_circ_86680,RMVar_hsa_circ_181586,RMVar_hsa_circ_181587 104172 RMVar_ID_104172 Human_SNP_ID_615762185 m1A Human chr17 - 5023983 5023983 5023983 TTGTGCTTTTTGGGCTGGAAGTGCTGGGGTTCAGGCTGTGCAGAACCCGCTCCCCGGGATCGGCC TTGTGCTTTTTGGGCTGGAAGTGCTGGGGTTCGGGCTGTGCAGAACCCGCTCCCCGGGATCGGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:5023776..5024050 26863410 MeRIP-seq:(Medium) rs1370741069 Functional Loss SNV dbSNP153 33..33 33 - - - 104173 RMVar_ID_104173 Human_SNP_ID_615762413 m1A Human chr17 + 5024517 5024516 5024517 GGGGGAAAGTGGGAGAGGACTGAGAGTGAGGCAAGTTCTCCCCAGCCCCTGTCCGTCTGTCTGTC GGGGGAAAGTGGGAGAGGACTGAGAGTGAGGC_AGTTCTCCCCAGCCCCTGTCCGTCTGTCTGTC CA C KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:5024466..5024725 26863196 MeRIP-seq:(Medium) rs1279303542 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_493832,Human_RBP_ID_1090836,Human_RBP_ID_3949982,Human_RBP_ID_4475944,Human_RBP_ID_5115346,Human_RBP_ID_5143081,Human_RBP_ID_5318211,Human_RBP_ID_6613347,Human_RBP_ID_22585150,Human_RBP_ID_23735062,Human_RBP_ID_26457065 Human_miRNA_ID_2073033,Human_miRNA_ID_2074714,Human_miRNA_ID_2367901,Human_miRNA_ID_2685656,Human_miRNA_ID_3015686,Human_miRNA_ID_3064875 RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_181583,RMVar_hsa_circ_75706,RMVar_hsa_circ_119211,RMVar_hsa_circ_181585,RMVar_hsa_circ_86680,RMVar_hsa_circ_181586,RMVar_hsa_circ_181587 104174 RMVar_ID_104174 Human_SNP_ID_615786575 m1A Human chr17 + 5109766 5109757 5109766 CCCATCATCATCATCTTCTCTTGTCCCTGTGTACCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG CCCATCATCATCATCTTCTCTTGT_________CCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG TCCCTGTGTA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5109733..5109798 26863196 MeRIP-seq:(Medium) rs912685649 Functional Loss DEL dbSNP153 25..33 33 - - - 104175 RMVar_ID_104175 Human_SNP_ID_615786577 m1A Human chr17 + 5109766 5109766 5109766 CCCATCATCATCATCTTCTCTTGTCCCTGTGTACCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG CCCATCATCATCATCTTCTCTTGTCCCTGTGTGCCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5109733..5109798 26863196 MeRIP-seq:(Medium) rs770758794 Functional Loss SNV dbSNP153 33..33 33 - - - 104176 RMVar_ID_104176 Human_SNP_ID_615808525 m1A Human chr17 + 5191881 5191867 5191882 GCCAGGCGAGAACTTCCGGTGCGCTCCCCGGGACTGCGGTCCCCCAGTCCGCGCCCCGCCCAGCC GCCAGGCGAGAACTTCCGG_______________TGCGGTCCCCCAGTCCGCGCCCCGCCCAGCC GTGCGCTCCCCGGGAC G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:5191781..5191951 26863196 MeRIP-seq:(Medium) rs1365569622 Functional Loss DEL dbSNP153 20..34 33 - - - 104177 RMVar_ID_104177 Human_SNP_ID_615808528 m1A Human chr17 + 5191881 5191881 5191881 GCCAGGCGAGAACTTCCGGTGCGCTCCCCGGGACTGCGGTCCCCCAGTCCGCGCCCCGCCCAGCC GCCAGGCGAGAACTTCCGGTGCGCTCCCCGGGCCTGCGGTCCCCCAGTCCGCGCCCCGCCCAGCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:5191781..5191951 26863196 MeRIP-seq:(Medium) rs373204081 Functional Loss SNV dbSNP153 33..33 33 - - - 104178 RMVar_ID_104178 Human_SNP_ID_615833164 m1A Human chr17 - 5282369 5282369 5282369 CAACCGAGCCGCCGCCGCCGCCGCCCAGAGAGAAACCGCTAAGGCTGGATCCGCCGGCGCCGCCA CAACCGAGCCGCCGCCGCCGCCGCCCAGAGAGGAACCGCTAAGGCTGGATCCGCCGGCGCCGCCA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:5282298..5282389 26863410 MeRIP-seq:(Medium) rs11538946 Functional Loss SNV dbSNP153 33..33 33 - - - 104179 RMVar_ID_104179 Human_SNP_ID_615833165 m1A Human chr17 - 5282369 5282369 5282369 CAACCGAGCCGCCGCCGCCGCCGCCCAGAGAGAAACCGCTAAGGCTGGATCCGCCGGCGCCGCCA CAACCGAGCCGCCGCCGCCGCCGCCCAGAGAGCAACCGCTAAGGCTGGATCCGCCGGCGCCGCCA T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:5282298..5282389 26863410 MeRIP-seq:(Medium) rs11538946 Functional Loss SNV dbSNP153 33..33 33 - - - 104180 RMVar_ID_104180 Human_SNP_ID_615833177 m1A Human chr17 - 5282400 5282400 5282400 CTCCCGCGGGCTCAGCTGGCGGAGGAGGCGTCAACCGAGCCGCCGCCGCCGCCGCCCAGAGAGAA CTCCCGCGGGCTCAGCTGGCGGAGGAGGCGTCGACCGAGCCGCCGCCGCCGCCGCCCAGAGAGAA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:5282276..5283927 26863410 MeRIP-seq:(Medium) rs1359158667 Functional Loss SNV dbSNP153 33..33 33 - - - 104181 RMVar_ID_104181 Human_SNP_ID_615834445 m1A Human chr17 + 5286840 5286840 5286840 TGATACGGGTTGTTAGATGATAAGTGCAATGGAAAAAAGAAAACAGAGCAGGAGAAAGGGAAGGG TGATACGGGTTGTTAGATGATAAGTGCAATGGGAAAAAGAAAACAGAGCAGGAGAAAGGGAAGGG A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5286838..5287119 26863196 MeRIP-seq:(Medium) rs1346253779 Functional Loss SNV dbSNP153 33..33 33 - - - 104182 RMVar_ID_104182 Human_SNP_ID_615847795 m1A Human chr17 + 5335288 5335286 5335289 GAGAATCCGCAGAGAGGGAAATAGCTGATTTAAGAAGAAGGCTGTCTGAAGGTCAAGAGGAGGAA GAGAATCCGCAGAGAGGGAAATAGCTGATTT___AAGAAGGCTGTCTGAAGGTCAAGAGGAGGAA TAAG T RABEP1 Ensembl:ENSG00000029725 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5335239..5335383 26863196 MeRIP-seq:(Medium) rs1360506544 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_46824,Human_RBP_ID_493919,Human_RBP_ID_1537423,Human_RBP_ID_2512961,Human_RBP_ID_4476003,Human_RBP_ID_5577562,Human_RBP_ID_6614532,Human_RBP_ID_9375210,Human_RBP_ID_13076808,Human_RBP_ID_23735363 Human_Splice_Rec_1766615,Human_Splice_Rec_1766647,Human_Splice_Rec_1766675,Human_Splice_Rec_1766703 RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_292747,RMVar_hsa_circ_181602,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_181606,RMVar_hsa_circ_78581,RMVar_hsa_circ_338442,RMVar_hsa_circ_369048,RMVar_hsa_circ_74920,RMVar_hsa_circ_181611,RMVar_hsa_circ_309914,RMVar_hsa_circ_181609,RMVar_hsa_circ_181608,RMVar_hsa_circ_321929,RMVar_hsa_circ_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632 104183 RMVar_ID_104183 Human_SNP_ID_615847806 m1A Human chr17 + 5335313 5335311 5335314 TGATTTAAGAAGAAGGCTGTCTGAAGGTCAAGAGGAGGAAAATTTAGAAAATGAAATGAAAAAGG TGATTTAAGAAGAAGGCTGTCTGAAGGTCAA___GAGGAAAATTTAGAAAATGAAATGAAAAAGG AGAG A RABEP1 Ensembl:ENSG00000029725 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:5335262..5335369 26863196 MeRIP-seq:(Medium) rs750489328 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_46824,Human_RBP_ID_493919,Human_RBP_ID_1009225,Human_RBP_ID_1863055,Human_RBP_ID_6614532,Human_RBP_ID_9375210,Human_RBP_ID_13076808,Human_RBP_ID_22954222,Human_RBP_ID_24372150 Human_Splice_Rec_1766615,Human_Splice_Rec_1766647,Human_Splice_Rec_1766675,Human_Splice_Rec_1766703 RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_292747,RMVar_hsa_circ_181602,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_181606,RMVar_hsa_circ_78581,RMVar_hsa_circ_338442,RMVar_hsa_circ_369048,RMVar_hsa_circ_74920,RMVar_hsa_circ_181611,RMVar_hsa_circ_309914,RMVar_hsa_circ_181609,RMVar_hsa_circ_181608,RMVar_hsa_circ_321929,RMVar_hsa_circ_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632 104184 RMVar_ID_104184 Human_SNP_ID_615854497 m1A Human chr17 - 5361478 5361478 5361478 AAACCCACTTGGCATCTGGAGTGACCCAAGGGATGCAGTATCAAAGTTCTCAGACACTGAATCTG AAACCCACTTGGCATCTGGAGTGACCCAAGGGTTGCAGTATCAAAGTTCTCAGACACTGAATCTG T A NUP88 Ensembl:ENSG00000108559 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:5361430..5361531 32194978 MeRIP-seq:(Medium) rs1365848456 Functional Loss SNV dbSNP153 33..33 33 - - - 104185 RMVar_ID_104185 Human_SNP_ID_615859788 m1A Human chr17 - 5378631 5378628 5378632 TAAATCAAGGAACAGTGAGGTCAGGAAGTTGAATGGGGTTACTATGAAAGGAACTAATGATGTCT TAAATCAAGGAACAGTGAGGTCAGGAAGTTG____GGGTTACTATGAAAGGAACTAATGATGTCT CCATT C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:5378627..5378931 26863196 MeRIP-seq:(Medium) rs1293898892 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_13077405 104186 RMVar_ID_104186 Human_SNP_ID_615862461 m1A Human chr17 - 5387398 5387398 5387398 CAAATATGAGGAAGCTAAAGAAAAACAAGAGGATATCATGAACAGGTCAGTGGGCTGTATAACAT CAAATATGAGGAAGCTAAAGAAAAACAAGAGGGTATCATGAACAGGTCAGTGGGCTGTATAACAT T C NUP88 Ensembl:ENSG00000108559 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5386816..5387477 32194978 MeRIP-seq:(Medium) rs1187336872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1863169,Human_RBP_ID_3528812,Human_RBP_ID_9377418 Human_Splice_Rec_1766722,Human_Splice_Rec_1766723,Human_Splice_Rec_1766754,Human_Splice_Rec_1766755,Human_Splice_Rec_1766786,Human_Splice_Rec_1766787,Human_Splice_Rec_1766800,Human_Splice_Rec_1766801,Human_Splice_Rec_1766813 RMVar_hsa_circ_81020,RMVar_hsa_circ_181639,RMVar_hsa_circ_265217,RMVar_hsa_circ_361041,RMVar_hsa_circ_85277,RMVar_hsa_circ_8958,RMVar_hsa_circ_181642,RMVar_hsa_circ_181643,RMVar_hsa_circ_181644,RMVar_hsa_circ_103669,RMVar_hsa_circ_266021,RMVar_hsa_circ_181645 104187 RMVar_ID_104187 Human_SNP_ID_615870646 m1A Human chr17 + 5416675 5416675 5416675 GATAGATTTCAAACAGGGGTGGATTTATGCAAAGCAATCTCTGAAAATTAGAGCAAACCAGTCAA GATAGATTTCAAACAGGGGTGGATTTATGCAATGCAATCTCTGAAAATTAGAGCAAACCAGTCAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5414077..5418037 32194978 MeRIP-seq:(Medium) rs1325207709 Functional Loss SNV dbSNP153 33..33 33 - - - 104188 RMVar_ID_104188 Human_SNP_ID_615871513 m1A Human chr17 + 5419521 5419510 5419522 CTGCGGCGGCGGCGACGAAGGCAACGACGAAGAAGCTGGTTTCTCAGCTTCGGTTGGACTCTGGT CTGCGGCGGCGGCGACGAAGGC____________GCTGGTTTCTCAGCTTCGGTTGGACTCTGGT CAACGACGAAGAA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5419360..5419561 32194978 MeRIP-seq:(Medium) rs940484196 Functional Loss DEL dbSNP153 23..34 33 - - - 104189 RMVar_ID_104189 Human_SNP_ID_615871583 m1A Human chr17 - 5419622 5419622 5419622 CAAGATGGCGGCCGCCGAGGGACCGGTGGGCGACGGCGAGCTGTGGCAGACCTGGCTTCCTAACC CAAGATGGCGGCCGCCGAGGGACCGGTGGGCGTCGGCGAGCTGTGGCAGACCTGGCTTCCTAACC T A NUP88 Ensembl:ENSG00000108559 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:5419398..5419675;chr17:5419425..5419675 26863196 MeRIP-seq:(Medium) rs1163929966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237640,Human_RBP_ID_768212,Human_RBP_ID_4465095,Human_RBP_ID_5466717,Human_RBP_ID_18990219,Human_RBP_ID_23129461 104190 RMVar_ID_104190 Human_SNP_ID_615874723 m1A Human chr17 + 5431117 5431117 5431117 GGTGAGTGCTGTGCAGCAGTCTTGGAGATCATAGTTGACAGTGCCGGCTCTGGGGTGGGCAGGAA GGTGAGTGCTGTGCAGCAGTCTTGGAGATCATGGTTGACAGTGCCGGCTCTGGGGTGGGCAGGAA A G RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:5431066..5431208 26863196 MeRIP-seq:(Medium) rs770188072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6615963,Human_RBP_ID_13080878 104191 RMVar_ID_104191 Human_SNP_ID_615874957 m1A Human chr17 + 5431545 5431543 5431546 AGACAAAATTGTATTCTGTAGGTCTTGAGTTCAACATTTGGAAAGGTAGACATTTGGAATGCTCT AGACAAAATTGTATTCTGTAGGTCTTGAGTT___CATTTGGAAAGGTAGACATTTGGAATGCTCT TCAA T RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:5431537..5431737 26863196 MeRIP-seq:(Medium) rs1445261224 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1863340,Human_RBP_ID_13080889 104192 RMVar_ID_104192 Human_SNP_ID_615875005 m1A Human chr17 + 5431651 5431651 5431651 GGACCATTGTGTTAGAATCCAGTGAGGTCAGGACGTAGGGACGCTCAGGACAGATGGCTGAGGAT GGACCATTGTGTTAGAATCCAGTGAGGTCAGGGCGTAGGGACGCTCAGGACAGATGGCTGAGGAT A G RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:5431435..5431720 26863196 MeRIP-seq:(Medium) rs775155584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6615971,Human_RBP_ID_13080898 104193 RMVar_ID_104193 Human_SNP_ID_615875439 m1A Human chr17 - 5433086 5433086 5433086 ACAACACTTTTGCAGATGAGCTGGTGGAGCTCAGCACAGCCCTGGAGCACCAGGAGTACATTACT ACAACACTTTTGCAGATGAGCTGGTGGAGCTCGGCACAGCCCTGGAGCACCAGGAGTACATTACT T C C1QBP Ensembl:ENSG00000108561 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5432901..5433451 32194978 MeRIP-seq:(Medium) rs375121100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235864,Human_RBP_ID_278396,Human_RBP_ID_494238,Human_RBP_ID_764732,Human_RBP_ID_1537597,Human_RBP_ID_1863356,Human_RBP_ID_4439600,Human_RBP_ID_6616019,Human_RBP_ID_8457366,Human_RBP_ID_9375225,Human_RBP_ID_13080978,Human_RBP_ID_17263788,Human_RBP_ID_17494867,Human_RBP_ID_17692539,Human_RBP_ID_17904160,Human_RBP_ID_18702964,Human_RBP_ID_19078147,Human_RBP_ID_22442756,Human_RBP_ID_22499939,Human_RBP_ID_22760683 Human_Splice_Rec_1767004,Human_Splice_Rec_1767014,Human_Splice_Rec_1767024,Human_Splice_Rec_1767026,Human_Splice_Rec_1767030 Human_miRNA_ID_624585 RMVar_hsa_circ_120727,RMVar_hsa_circ_181667,RMVar_hsa_circ_181668 104194 RMVar_ID_104194 Human_SNP_ID_615875465 m1A Human chr17 - 5433154 5433154 5433154 TAGTAAATATTGTTCTTTGCAGGCCTTATATGACCACCTAATGGATTTCCTTGCCGACCGAGGGG TAGTAAATATTGTTCTTTGCAGGCCTTATATGGCCACCTAATGGATTTCCTTGCCGACCGAGGGG T C C1QBP Ensembl:ENSG00000108561 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1186258998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_494243,Human_RBP_ID_1287532,Human_RBP_ID_1537599,Human_RBP_ID_9073756,Human_RBP_ID_17654500,Human_RBP_ID_17904644,Human_RBP_ID_24479830,Human_RBP_ID_26453350,Human_RBP_ID_26811860 Human_Splice_Rec_1767004,Human_Splice_Rec_1767014,Human_Splice_Rec_1767024,Human_Splice_Rec_1767026,Human_Splice_Rec_1767030 RMVar_hsa_circ_120727,RMVar_hsa_circ_181667,RMVar_hsa_circ_181668 104195 RMVar_ID_104195 Human_SNP_ID_615875466 m1A Human chr17 + 5433161 5433161 5433161 GTCGGCAAGGAAATCCATTAGGTGGTCATATAAGGCCTGCAAAGAACAATATTTACTAGTTAAAA GTCGGCAAGGAAATCCATTAGGTGGTCATATAGGGCCTGCAAAGAACAATATTTACTAGTTAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5432953..5433188 26863196 MeRIP-seq:(Medium) rs1804437 Functional Loss SNV dbSNP153 33..33 33 - - - 104196 RMVar_ID_104196 Human_SNP_ID_615877385 m1A Human chr17 + 5439011 5439002 5439011 AGGAGCTGCCGGAAAGGCGAGGCGGGCGCGGCAGCGCGGAGGCCGGCGACGGAGGAGCCCAGCAC AGGAGCTGCCGGAAAGGCGAGGCG_________GCGCGGAGGCCGGCGACGGAGGAGCCCAGCAC GGGCGCGGCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:5438826..5439175 26863410 MeRIP-seq:(Medium) rs1567593270 Functional Loss DEL dbSNP153 25..33 33 - - - 104197 RMVar_ID_104197 Human_SNP_ID_615877402 m1A Human chr17 + 5439044 5439044 5439044 GCGCGGAGGCCGGCGACGGAGGAGCCCAGCACACGGGGCACGCAGCGCAGCAGAGGCAGCATCGC GCGCGGAGGCCGGCGACGGAGGAGCCCAGCACCCGGGGCACGCAGCGCAGCAGAGGCAGCATCGC A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:5438947..5439103 26863410 MeRIP-seq:(Medium) rs1567593301 Functional Loss SNV dbSNP153 33..33 33 - - - 104198 RMVar_ID_104198 Human_SNP_ID_615884912 m1A Human chr17 + 5468027 5468027 5468027 TCTGCTCACTCTCTATTCCTTTGACTAGCAGCACTCATGGGTCTCCTTCCTCTCTTTGGCTGCTC TCTGCTCACTCTCTATTCCTTTGACTAGCAGCCCTCATGGGTCTCCTTCCTCTCTTTGGCTGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5468017..5468286 26863196 MeRIP-seq:(Medium) rs1356549984 Functional Loss SNV dbSNP153 33..33 33 - - - 104199 RMVar_ID_104199 Human_SNP_ID_615890201 m1A Human chr17 + 5488349 5488349 5488349 AGAGGGTGGAGGGGCTGTAAATCTTGAAGATTAGGGTATAATATGAGTATATGGGTAAGAATTGG AGAGGGTGGAGGGGCTGTAAATCTTGAAGATTGGGGTATAATATGAGTATATGGGTAAGAATTGG A G MIS12 Ensembl:ENSG00000167842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5488175..5488461 26863196 MeRIP-seq:(Medium) rs1484780569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_494522,Human_RBP_ID_22954391 104200 RMVar_ID_104200 Human_SNP_ID_615893319 m1A Human chr17 + 5500746 5500746 5500746 TGGAGGCGCCTCCTTCTTGGGCGGGGGGCGCGATGCGGCCTTCGGGGGCTGCCCGGCGCGGCCCC TGGAGGCGCCTCCTTCTTGGGCGGGGGGCGCGGTGCGGCCTTCGGGGGCTGCCCGGCGCGGCCCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:5500702..5500952 32194978 MeRIP-seq:(Medium) rs901545038 Functional Loss SNV dbSNP153 33..33 33 - - - 104201 RMVar_ID_104201 Human_SNP_ID_615893320 m1A Human chr17 + 5500746 5500746 5500746 TGGAGGCGCCTCCTTCTTGGGCGGGGGGCGCGATGCGGCCTTCGGGGGCTGCCCGGCGCGGCCCC TGGAGGCGCCTCCTTCTTGGGCGGGGGGCGCGTTGCGGCCTTCGGGGGCTGCCCGGCGCGGCCCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:5500702..5500952 32194978 MeRIP-seq:(Medium) rs901545038 Functional Loss SNV dbSNP153 33..33 33 - - - 104202 RMVar_ID_104202 Human_SNP_ID_615893395 m1A Human chr17 - 5500901 5500901 5500901 CAGACCCTGGGGTCTCGAGCAGATTCGCCCGGACCCCGAGTCCGAAGGCCTGTTTGACAAGCCTC CAGACCCTGGGGTCTCGAGCAGATTCGCCCGGTCCCCGAGTCCGAAGGCCTGTTTGACAAGCCTC T A NLRP1,AC055839.2 Ensembl:ENSG00000091592,Ensembl:ENSG00000286190 Protein coding,Protein coding intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5500851..5500952 32194978 MeRIP-seq:(Medium) rs1421416627 Functional Loss SNV dbSNP153 33..33 33 - - - 104203 RMVar_ID_104203 Human_SNP_ID_616038638 m1A Human chr17 - 6070654 6070654 6070654 GGGTCCGGCTGGAGCGCCGAGAGACAGGACTCACCCCGCGATCGCGGCCGGCTGGGGCGCCCGCA GGGTCCGGCTGGAGCGCCGAGAGACAGGACTCGCCCCGCGATCGCGGCCGGCTGGGGCGCCCGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:6070458..6070703 26863196 MeRIP-seq:(Medium) rs933298009 Functional Loss SNV dbSNP153 33..33 33 - - - 104204 RMVar_ID_104204 Human_SNP_ID_616040906 m1A Human chr17 + 6080325 6080325 6080325 GTGAGGGGTGTCCCAGCCTGGGAGTGCCAGGTAGTGGACCCGCCTATTACATCTCGGTGCTCTTT GTGAGGGGTGTCCCAGCCTGGGAGTGCCAGGTGGTGGACCCGCCTATTACATCTCGGTGCTCTTT A G WSCD1,AC007846.2 Ensembl:ENSG00000179314,Ensembl:ENSG00000285471 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6080324..6080529 26863196 MeRIP-seq:(Medium) rs1489130972 Functional Loss SNV dbSNP153 33..33 33 - - - 104205 RMVar_ID_104205 Human_SNP_ID_616040914 m1A Human chr17 - 6080346 6080346 6080346 GCAGAAATCTGGAAGGTGGAGAAAGAGCACCGAGATGTAATAGGCGGGTCCACTACCTGGCACTC GCAGAAATCTGGAAGGTGGAGAAAGAGCACCGCGATGTAATAGGCGGGTCCACTACCTGGCACTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:6080344..6080463 26863196 MeRIP-seq:(Medium) rs529783421 Functional Loss SNV dbSNP153 33..33 33 - - - 104206 RMVar_ID_104206 Human_SNP_ID_616043691 m1A Human chr17 + 6090416 6090416 6090416 GGTGAGCGTGGGGCTGGAAGAGTGTAACCATGAGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGG GGTGAGCGTGGGGCTGGAAGAGTGTAACCATGGGTGCAAAGGCGAGAAGGGCTCTGTGTGCGGGG A G WSCD1 Ensembl:ENSG00000179314 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:6090366..6090465 26863196 MeRIP-seq:(Medium) rs766340121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23741539 Human_Splice_Rec_1767644,Human_Splice_Rec_1767645,Human_Splice_Rec_1767658,Human_Splice_Rec_1767659,Human_Splice_Rec_1767678,Human_Splice_Rec_1767679,Human_Splice_Rec_1767694,Human_Splice_Rec_1767695,Human_Splice_Rec_1767710,Human_Splice_Rec_1767711,Human_Splice_Rec_1767726,Human_Splice_Rec_1767727,Human_Splice_Rec_1767742 RMVar_hsa_circ_265344,RMVar_hsa_circ_273215,RMVar_hsa_circ_181704,RMVar_hsa_circ_181706,RMVar_hsa_circ_309689,RMVar_hsa_circ_343013,RMVar_hsa_circ_181705 104207 RMVar_ID_104207 Human_SNP_ID_616147555 m1A Human chr17 - 6474481 6474481 6474481 GATGTGTCCGACTTCTTCCTCTTCGGCTCGCCACTGGGCCTGGTCCTGGCCATGCGGAGGACGGT GATGTGTCCGACTTCTTCCTCTTCGGCTCGCCTCTGGGCCTGGTCCTGGCCATGCGGAGGACGGT T A PITPNM3 Ensembl:ENSG00000091622 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:6474347..6474552 26863196 MeRIP-seq:(Medium) rs777390006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1767921,Human_Splice_Rec_1767957,Human_Splice_Rec_1768003 RMVar_hsa_circ_108072,RMVar_hsa_circ_78698,RMVar_hsa_circ_98941,RMVar_hsa_circ_181714,RMVar_hsa_circ_181715,RMVar_hsa_circ_96933,RMVar_hsa_circ_181716,RMVar_hsa_circ_181717 104208 RMVar_ID_104208 Human_SNP_ID_616149563 m1A Human chr17 - 6481997 6481997 6481997 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGTTCTGTTTTCCTAGGGCTAA AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGAGAGAGAGGTTCTGTTTTCCTAGGGCTAA T C PITPNM3 Ensembl:ENSG00000091622 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:6481977..6482061 26863410 MeRIP-seq:(Medium) rs1446018746 Functional Loss SNV dbSNP153 33..33 33 - - - 104209 RMVar_ID_104209 Human_SNP_ID_616167786 m1A Human chr17 + 6556491 6556491 6556491 GCCCGGCCCCGACCGCCTCCGGCCCCGAACGGACTCCGAGCGCCGCGCCCGCGCCCCCGCCCCGC GCCCGGCCCCGACCGCCTCCGGCCCCGAACGGGCTCCGAGCGCCGCGCCCGCGCCCCCGCCCCGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:6556385..6556552 26863196 MeRIP-seq:(Medium) rs1476045946 Functional Loss SNV dbSNP153 33..33 33 - - - 104210 RMVar_ID_104210 Human_SNP_ID_616167799 m1A Human chr17 - 6556529 6556529 6556529 CGAGGCGGCGGCGGCTGCGGTGGCGGCAGCCGAGGCGAGCGGGGCGGGGGCGCGGGCGCGGCGCT CGAGGCGGCGGCGGCTGCGGTGGCGGCAGCCGGGGCGAGCGGGGCGGGGGCGCGGGCGCGGCGCT T C PITPNM3 Ensembl:ENSG00000091622 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:6556387..6556561;chr17:6537988..6556569 26863196 MeRIP-seq:(Medium) rs1271915513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181719 104211 RMVar_ID_104211 Human_SNP_ID_616168856 m1A Human chr17 - 6560705 6560653 6560705 AGGAGGAGAAGGAGGAGGAGGAAGAGGAGGAGAAGAGAGAGAATGAGAAGGAGGATAATGAGAGG AGGAGGAGAAGGAGGAGGAGGAAGAGGAGGAG_________________________________ CCCCTCCTCCTCTTCCTCCTCCTCTCATTATCCTCCTTCTCATTCTCTCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6560685..6560768 26863196 MeRIP-seq:(Medium) rs1567703358 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_181719 104212 RMVar_ID_104212 Human_SNP_ID_616168860 m1A Human chr17 - 6560705 6560655 6560705 AGGAGGAGAAGGAGGAGGAGGAAGAGGAGGAGAAGAGAGAGAATGAGAAGGAGGATAATGAGAGG AGGAGGAGAAGGAGGAGGAGGAAGAGGAGGAG_________________________________ CCTCCTCCTCTTCCTCCTCCTCTCATTATCCTCCTTCTCATTCTCTCTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6560685..6560768 26863196 MeRIP-seq:(Medium) rs1357607432 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_181719 104213 RMVar_ID_104213 Human_SNP_ID_616169475 m1A Human chr17 - 6561301 6561298 6561301 GGAGAAAGAAGAGAAGGAGGAAGAGGCAGAAGAAGGGAGAAGGAGGAGGAAGAGGAGGAGGAGGG GGAGAAAGAAGAGAAGGAGGAAGAGGCAGAAG___GGAGAAGGAGGAGGAAGAGGAGGAGGAGGG CCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6561258..6561359 26863196 MeRIP-seq:(Medium) rs1474410092 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_181719 104214 RMVar_ID_104214 Human_SNP_ID_616169617 m1A Human chr17 - 6561454 6561452 6561455 AGGAGGAAGAGGAGGAGGGGAGAAAGAAGAGGAGAAGGAGGAAGAGGAAGGGAGAAGGAGGAGGA AGGAGGAAGAGGAGGAGGGGAGAAAGAAGAG___AAGGAGGAAGAGGAAGGGAGAAGGAGGAGGA TCTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6561425..6561598 26863196 MeRIP-seq:(Medium) rs774113894 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_181719 104215 RMVar_ID_104215 Human_SNP_ID_616174708 m1A Human chr17 - 6579726 6579726 6579726 GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCATTTGTGTCACACTGGAGAAGGGATGGCACCAC GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCTTTTGTGTCACACTGGAGAAGGGATGGCACCAC T A KIAA0753 Ensembl:ENSG00000198920 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3744720 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13461,GWAS_ID_13462,GWAS_ID_13463,GWAS_ID_13464,GWAS_ID_13465,GWAS_ID_13466,GWAS_ID_13467,GWAS_ID_13468,GWAS_ID_13469,GWAS_ID_13470,GWAS_ID_13471,GWAS_ID_13472,GWAS_ID_13473,GWAS_ID_13474,GWAS_ID_13475,GWAS_ID_13476,GWAS_ID_13477,GWAS_ID_13478,GWAS_ID_13479,GWAS_ID_13480,GWAS_ID_13481,GWAS_ID_13482,GWAS_ID_13483,GWAS_ID_13484,GWAS_ID_13485,GWAS_ID_13486,GWAS_ID_13487,GWAS_ID_13488,GWAS_ID_13489,GWAS_ID_13490,GWAS_ID_13491,GWAS_ID_13492,GWAS_ID_13493,GWAS_ID_13494,GWAS_ID_13495,GWAS_ID_13496,GWAS_ID_13497,GWAS_ID_13498,GWAS_ID_13499,GWAS_ID_13500,GWAS_ID_13501,GWAS_ID_13502,GWAS_ID_13503,GWAS_ID_13504,GWAS_ID_13505,GWAS_ID_13506,GWAS_ID_13507,GWAS_ID_13508,GWAS_ID_13509 RMVar_hsa_circ_181719 104216 RMVar_ID_104216 Human_SNP_ID_616174709 m1A Human chr17 - 6579726 6579726 6579726 GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCATTTGTGTCACACTGGAGAAGGGATGGCACCAC GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCGTTTGTGTCACACTGGAGAAGGGATGGCACCAC T C KIAA0753 Ensembl:ENSG00000198920 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3744720 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_13461,GWAS_ID_13462,GWAS_ID_13463,GWAS_ID_13464,GWAS_ID_13465,GWAS_ID_13466,GWAS_ID_13467,GWAS_ID_13468,GWAS_ID_13469,GWAS_ID_13470,GWAS_ID_13471,GWAS_ID_13472,GWAS_ID_13473,GWAS_ID_13474,GWAS_ID_13475,GWAS_ID_13476,GWAS_ID_13477,GWAS_ID_13478,GWAS_ID_13479,GWAS_ID_13480,GWAS_ID_13481,GWAS_ID_13482,GWAS_ID_13483,GWAS_ID_13484,GWAS_ID_13485,GWAS_ID_13486,GWAS_ID_13487,GWAS_ID_13488,GWAS_ID_13489,GWAS_ID_13490,GWAS_ID_13491,GWAS_ID_13492,GWAS_ID_13493,GWAS_ID_13494,GWAS_ID_13495,GWAS_ID_13496,GWAS_ID_13497,GWAS_ID_13498,GWAS_ID_13499,GWAS_ID_13500,GWAS_ID_13501,GWAS_ID_13502,GWAS_ID_13503,GWAS_ID_13504,GWAS_ID_13505,GWAS_ID_13506,GWAS_ID_13507,GWAS_ID_13508,GWAS_ID_13509 RMVar_hsa_circ_181719 104217 RMVar_ID_104217 Human_SNP_ID_616175664 m1A Human chr17 - 6583474 6583474 6583474 AGAGGAGGTAAGAAGGTCTAACGTGTTGTTGGAATCTCAGGTCAGGAGAGAGAGAAAACGAGTCA AGAGGAGGTAAGAAGGTCTAACGTGTTGTTGGCATCTCAGGTCAGGAGAGAGAGAAAACGAGTCA T G KIAA0753 Ensembl:ENSG00000198920 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:6583447..6583578 26863196 MeRIP-seq:(Medium) rs1567530707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1867541,Human_RBP_ID_13137736 RMVar_hsa_circ_181719 104218 RMVar_ID_104218 Human_SNP_ID_616175673 m1A Human chr17 - 6583520 6583520 6583520 ACACACAAAAAAAGACGAAAAGTGAAGAAGAGAGGGAAAGGGACATAGAGGAGGTAAGAAGGTCT ACACACAAAAAAAGACGAAAAGTGAAGAAGAGTGGGAAAGGGACATAGAGGAGGTAAGAAGGTCT T A KIAA0753 Ensembl:ENSG00000198920 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:6583421..6583567 26863196 MeRIP-seq:(Medium) rs779180227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181719 104219 RMVar_ID_104219 Human_SNP_ID_616177120 m1A Human chr17 + 6589899 6589899 6589899 CGATGCTGTGCTGCATACCCGGTGGGACAAAGAGGGGAGCTCGGCCTTCTTTCTGTTGAGAATCT CGATGCTGTGCTGCATACCCGGTGGGACAAAGCGGGGAGCTCGGCCTTCTTTCTGTTGAGAATCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:6589850..6589955 32194978 MeRIP-seq:(Medium) rs1337266033 Functional Loss SNV dbSNP153 33..33 33 - - - 104220 RMVar_ID_104220 Human_SNP_ID_616181752 m1A Human chr17 + 6608461 6608461 6608461 TCTCTGGGGCTAGTTTTCACCTTTAGCCATGCAGCACTGAAATAAATGGAAAAGCATACCTTTGT TCTCTGGGGCTAGTTTTCACCTTTAGCCATGCGGCACTGAAATAAATGGAAAAGCATACCTTTGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:6608459..6608586 26863196 MeRIP-seq:(Medium) rs4796519 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_13510,GWAS_ID_13511,GWAS_ID_13512,GWAS_ID_13513,GWAS_ID_13514,GWAS_ID_13515,GWAS_ID_13516,GWAS_ID_13517,GWAS_ID_13518,GWAS_ID_13519,GWAS_ID_13520,GWAS_ID_13521,GWAS_ID_13522,GWAS_ID_13523,GWAS_ID_13524,GWAS_ID_13525,GWAS_ID_13526,GWAS_ID_13527,GWAS_ID_13528,GWAS_ID_13529,GWAS_ID_13530,GWAS_ID_13531,GWAS_ID_13532,GWAS_ID_13533,GWAS_ID_13534,GWAS_ID_13535,GWAS_ID_13536,GWAS_ID_13537,GWAS_ID_13538,GWAS_ID_13539,GWAS_ID_13540,GWAS_ID_13541,GWAS_ID_13542,GWAS_ID_13543,GWAS_ID_13544,GWAS_ID_13545,GWAS_ID_13546,GWAS_ID_13547,GWAS_ID_13548,GWAS_ID_13549,GWAS_ID_13550,GWAS_ID_13551,GWAS_ID_13552,GWAS_ID_13553,GWAS_ID_13554,GWAS_ID_13555,GWAS_ID_13556,GWAS_ID_13557,GWAS_ID_13558,GWAS_ID_13559,GWAS_ID_13560 104221 RMVar_ID_104221 Human_SNP_ID_616188820 m1A Human chr17 + 6636660 6636660 6636660 TGTCCCTCTACATACCCTGGGGCATCTCCACGAAAACCCTCTCTCCCCCATGCTGAGATGCCCTT TGTCCCTCTACATACCCTGGGGCATCTCCACGCAAACCCTCTCTCCCCCATGCTGAGATGCCCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:6636461..6636866;chr17:6636610..6636881 26863196 MeRIP-seq:(Medium) rs1195966728 Functional Loss SNV dbSNP153 33..33 33 - - - 104222 RMVar_ID_104222 Human_SNP_ID_616189183 m1A Human chr17 - 6638081 6638081 6638081 GTGGTTCTGGGGCCTTCCCGGGCCCATGGGGGAGGAGACAGACTATTGGGGTTCCTGTGGTGCCT GTGGTTCTGGGGCCTTCCCGGGCCCATGGGGGGGGAGACAGACTATTGGGGTTCCTGTGGTGCCT T C AC004706.3,KIAA0753 Ensembl:ENSG00000282936,Ensembl:ENSG00000198920 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:6638030..6638298 26863196 MeRIP-seq:(Medium) rs1326143624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5582365,Human_RBP_ID_8093497,Human_RBP_ID_8189263 104223 RMVar_ID_104223 Human_SNP_ID_616189315 m1A Human chr17 + 6638517 6638517 6638517 GTCTCAGACACCCCCACAGCCTGCCTCCTCCCACACTGACATGCAACATCTCCACAGCCAGCCTC GTCTCAGACACCCCCACAGCCTGCCTCCTCCCCCACTGACATGCAACATCTCCACAGCCAGCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:6638472..6638573 26863196 MeRIP-seq:(Medium) rs574358907 Functional Loss SNV dbSNP153 33..33 33 - - - 104224 RMVar_ID_104224 Human_SNP_ID_616189792 m1A Human chr17 - 6640335 6640335 6640335 TAAGACATCCCCCAGGGCCGCGGTAGGGAGGAAGGGAACTGCCCTGGAGCTATGAGCCGGGAGAC TAAGACATCCCCCAGGGCCGCGGTAGGGAGGAGGGGAACTGCCCTGGAGCTATGAGCCGGGAGAC T C AC004706.3,KIAA0753 Ensembl:ENSG00000282936,Ensembl:ENSG00000198920 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:6639717..6640432 26863196 MeRIP-seq:(Medium) rs1054761138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542531,Human_RBP_ID_8189274,Human_RBP_ID_17189864,Human_RBP_ID_23745673 104225 RMVar_ID_104225 Human_SNP_ID_616190699 m1A Human chr17 + 6643137 6643137 6643137 ATAAATGATGTTAAAAAAACTGGCATGTGTCTAAACAATAGAGTGCTATTAAAATGCCCATGAAC ATAAATGATGTTAAAAAAACTGGCATGTGTCTGAACAATAGAGTGCTATTAAAATGCCCATGAAC A G TXNDC17 Ensembl:ENSG00000129235 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72835775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2520881,Human_RBP_ID_3535455 GWAS_ID_13561,GWAS_ID_13562,GWAS_ID_13563,GWAS_ID_13564,GWAS_ID_13565 RMVar_hsa_circ_181730,RMVar_hsa_circ_96198 104226 RMVar_ID_104226 Human_SNP_ID_616192908 m1A Human chr17 - 6651822 6651822 6651822 CAGGCAGAAGAGAGGAAAACTACGGTACTGCCATAGCCGGGAGCGCCACAACACGATGACGTGGA CAGGCAGAAGAGAGGAAAACTACGGTACTGCCGTAGCCGGGAGCGCCACAACACGATGACGTGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:6651774..6651933 26863196 MeRIP-seq:(Medium) rs528939179 Functional Loss SNV dbSNP153 33..33 33 - - - 104227 RMVar_ID_104227 Human_SNP_ID_616280018 m1A Human chr17 - 7002305 7002305 7002305 TTACCATGCTAACATACATCTCTATCCACCTTACTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG TTACCATGCTAACATACATCTCTATCCACCTTGCTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG T C AC040977.2,ALOX12-AS1 Ensembl:ENSG00000267047,Ensembl:ENSG00000215067 lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20263410 GWAS_ID_13566,GWAS_ID_13567,GWAS_ID_13568,GWAS_ID_13569,GWAS_ID_13570,GWAS_ID_13571,GWAS_ID_13572,GWAS_ID_13573,GWAS_ID_13574,GWAS_ID_13575,GWAS_ID_13576,GWAS_ID_13577,GWAS_ID_13578,GWAS_ID_13579,GWAS_ID_13580,GWAS_ID_13581,GWAS_ID_13582,GWAS_ID_13583,GWAS_ID_13584,GWAS_ID_13585,GWAS_ID_13586,GWAS_ID_13587,GWAS_ID_13588,GWAS_ID_13589,GWAS_ID_13590,GWAS_ID_13591 104228 RMVar_ID_104228 Human_SNP_ID_616280019 m1A Human chr17 - 7002305 7002305 7002305 TTACCATGCTAACATACATCTCTATCCACCTTACTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG TTACCATGCTAACATACATCTCTATCCACCTTCCTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG T G AC040977.2,ALOX12-AS1 Ensembl:ENSG00000267047,Ensembl:ENSG00000215067 lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20263410 GWAS_ID_13566,GWAS_ID_13567,GWAS_ID_13568,GWAS_ID_13569,GWAS_ID_13570,GWAS_ID_13571,GWAS_ID_13572,GWAS_ID_13573,GWAS_ID_13574,GWAS_ID_13575,GWAS_ID_13576,GWAS_ID_13577,GWAS_ID_13578,GWAS_ID_13579,GWAS_ID_13580,GWAS_ID_13581,GWAS_ID_13582,GWAS_ID_13583,GWAS_ID_13584,GWAS_ID_13585,GWAS_ID_13586,GWAS_ID_13587,GWAS_ID_13588,GWAS_ID_13589,GWAS_ID_13590,GWAS_ID_13591 104229 RMVar_ID_104229 Human_SNP_ID_616283133 m1A Human chr17 + 7012738 7012738 7012738 GGCCGAAGCTGGCCGCCTGCGGCATCGTCCTCAGCGCCTGGGGAGTGATCATGTTGGTGAGGGGA GGCCGAAGCTGGCCGCCTGCGGCATCGTCCTCGGCGCCTGGGGAGTGATCATGTTGGTGAGGGGA A G RNASEK-C17orf49,RNASEK Ensembl:ENSG00000161939,Ensembl:ENSG00000219200 Protein coding,Protein coding exon,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7012692..7012805 26863196 MeRIP-seq:(Medium) rs755632158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51018,Human_RBP_ID_237425,Human_RBP_ID_498572,Human_RBP_ID_767645,Human_RBP_ID_4464279,Human_RBP_ID_5144010,Human_RBP_ID_5318216,Human_RBP_ID_5497629,Human_RBP_ID_9326441,Human_RBP_ID_22443384,Human_RBP_ID_23746868,Human_RBP_ID_26769465 Human_Splice_Rec_1768853,Human_Splice_Rec_1768857,Human_Splice_Rec_1768863,Human_Splice_Rec_1768867,Human_Splice_Rec_1768871,Human_Splice_Rec_1768879,Human_Splice_Rec_1768881,Human_Splice_Rec_1768891,Human_Splice_Rec_1768903 104230 RMVar_ID_104230 Human_SNP_ID_616283140 m1A Human chr17 - 7012751 7012751 7012751 CCTTGCCGGGGAGTCCCCTCACCAACATGATCACTCCCCAGGCGCTGAGGACGATGCCGCAGGCG CCTTGCCGGGGAGTCCCCTCACCAACATGATCGCTCCCCAGGCGCTGAGGACGATGCCGCAGGCG T C AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7012626..7012775 26863196 MeRIP-seq:(Medium) rs1332800552 Functional Loss SNV dbSNP153 33..33 33 - - - 104231 RMVar_ID_104231 Human_SNP_ID_616283143 m1A Human chr17 + 7012756 7012756 7012756 GCGGCATCGTCCTCAGCGCCTGGGGAGTGATCATGTTGGTGAGGGGACTCCCCGGCAAGGATCGG GCGGCATCGTCCTCAGCGCCTGGGGAGTGATCCTGTTGGTGAGGGGACTCCCCGGCAAGGATCGG A C RNASEK-C17orf49,RNASEK Ensembl:ENSG00000161939,Ensembl:ENSG00000219200 Protein coding,Protein coding exon,CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7012684..7012823 26863410 MeRIP-seq:(Medium) rs779384222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498572,Human_RBP_ID_4464279,Human_RBP_ID_5497629,Human_RBP_ID_22445267,Human_RBP_ID_23746868 Human_Splice_Rec_1768853,Human_Splice_Rec_1768857,Human_Splice_Rec_1768863,Human_Splice_Rec_1768867,Human_Splice_Rec_1768871,Human_Splice_Rec_1768879,Human_Splice_Rec_1768881,Human_Splice_Rec_1768891,Human_Splice_Rec_1768903 104232 RMVar_ID_104232 Human_SNP_ID_616283268 m1A Human chr17 + 7013136 7013136 7013136 GACAGAGCGAGACTCCGTCCCCAAAGAAAAAGAAAAAAGGGAACTGGAGCGGAGGGCCCTGGAGT GACAGAGCGAGACTCCGTCCCCAAAGAAAAAGCAAAAAGGGAACTGGAGCGGAGGGCCCTGGAGT A C RNASEK-C17orf49,RNASEK Ensembl:ENSG00000161939,Ensembl:ENSG00000219200 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7013134..7013281 26863196 MeRIP-seq:(Medium) rs182066807 Functional Loss SNV dbSNP153 33..33 33 - - - 104233 RMVar_ID_104233 Human_SNP_ID_616283483 m1A Human chr17 - 7013740 7013740 7013740 CCAGCCCGCCTCCCCCACCCGAATACTTACTCAAAATCTTTCTCCGTGAAGGGAACGTCCTCAAT CCAGCCCGCCTCCCCCACCCGAATACTTACTCCAAATCTTTCTCCGTGAAGGGAACGTCCTCAAT T G AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7013651..7013758 26863196 MeRIP-seq:(Medium) rs752924899 Functional Loss SNV dbSNP153 33..33 33 - - - 104234 RMVar_ID_104234 Human_SNP_ID_616283606 m1A Human chr17 - 7014164 7014164 7014164 ACAGTTGTAGCTGACTTGCTCGTAAAGGTTGTATATGTTCTGGGGGCCATTCCTGGGGGTGGGAA ACAGTTGTAGCTGACTTGCTCGTAAAGGTTGTGTATGTTCTGGGGGCCATTCCTGGGGGTGGGAA T C AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7014126..7014475 26863196 MeRIP-seq:(Medium) rs1052004802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6640895 104235 RMVar_ID_104235 Human_SNP_ID_616283625 m1A Human chr17 - 7014225 7014225 7014225 TGAGCCGAACTTGGCAGAAAGAGAAGCCTCCGAGGAGGAGGTAAAGGCCTGCAGCGATGAAACAG TGAGCCGAACTTGGCAGAAAGAGAAGCCTCCGCGGAGGAGGTAAAGGCCTGCAGCGATGAAACAG T G AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7014186..7014419 26863196 MeRIP-seq:(Medium) rs748008725 Functional Loss SNV dbSNP153 33..33 33 - - - 104236 RMVar_ID_104236 Human_SNP_ID_616283678 m1A Human chr17 - 7014369 7014369 7014369 CCGGGAAACCCAGTCCCGCAGAGGGCGCCGGCAAGGGTGGGACGCGACCTGGGTGACACGGTGCA CCGGGAAACCCAGTCCCGCAGAGGGCGCCGGCGAGGGTGGGACGCGACCTGGGTGACACGGTGCA T C AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7014351..7014375 26863196 MeRIP-seq:(Medium) rs1214819080 Functional Loss SNV dbSNP153 33..33 33 - - - 104237 RMVar_ID_104237 Human_SNP_ID_616283707 m1A Human chr17 + 7014407 7014407 7014407 CGCCCTCTGCGGGACTGGGTTTCCCGGGCGAGAGACTGAATCCCTTCTCCCATCTCTGGCATCCG CGCCCTCTGCGGGACTGGGTTTCCCGGGCGAGGGACTGAATCCCTTCTCCCATCTCTGGCATCCG A G RNASEK-C17orf49,RNASEK Ensembl:ENSG00000161939,Ensembl:ENSG00000219200 Protein coding,Protein coding exon,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7014244..7014525 26863410 MeRIP-seq:(Medium) rs943676563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498586,Human_RBP_ID_1010268,Human_RBP_ID_5114502,Human_RBP_ID_8462000,Human_RBP_ID_13151101,Human_RBP_ID_17653652,Human_RBP_ID_18941277,Human_RBP_ID_20172850,Human_RBP_ID_23746879,Human_RBP_ID_26811874,Human_RBP_ID_27156756,Human_RBP_ID_27456200 RMVar_hsa_circ_92181,RMVar_hsa_circ_181740 104238 RMVar_ID_104238 Human_SNP_ID_616283911 m1A Human chr17 + 7014817 7014817 7014817 CTCCCTGCTCTCCGTGGTCCCGGCTCGCGTGTAGCGGCGGCGGCGGCGTCTCCGTGAGGAGGCGC CTCCCTGCTCTCCGTGGTCCCGGCTCGCGTGTGGCGGCGGCGGCGGCGTCTCCGTGAGGAGGCGC A G RNASEK-C17orf49,C17orf49 Ensembl:ENSG00000161939,Ensembl:ENSG00000258315 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7014776..7016703 26863196 MeRIP-seq:(Medium) rs1018062826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4448001 Human_Splice_Rec_1768907,Human_Splice_Rec_1768919,Human_Splice_Rec_1768933,Human_Splice_Rec_1768943,Human_Splice_Rec_1768951,Human_Splice_Rec_1768955,Human_Splice_Rec_1768963 RMVar_hsa_circ_92181,RMVar_hsa_circ_181740 104239 RMVar_ID_104239 Human_SNP_ID_616284790 m1A Human chr17 + 7017396 7017396 7017396 GATCTCCTGGGACTCCGAGCAAGGCCTGCACGAGAGAGGGCTGAAAGGCTGCTGGGGCTGCCACC GATCTCCTGGGACTCCGAGCAAGGCCTGCACGGGAGAGGGCTGAAAGGCTGCTGGGGCTGCCACC A G RNASEK-C17orf49,C17orf49 Ensembl:ENSG00000161939,Ensembl:ENSG00000258315 Protein coding,Protein coding exon,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7016935..7019414 32194978 MeRIP-seq:(Medium) rs1458344220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_498603,Human_RBP_ID_17378135,Human_RBP_ID_17654512,Human_RBP_ID_18942736 Human_miRNA_ID_175463,Human_miRNA_ID_175464,Human_miRNA_ID_1549553,Human_miRNA_ID_1549554,Human_miRNA_ID_1550063,Human_miRNA_ID_1550064,Human_miRNA_ID_2794484,Human_miRNA_ID_2794485,Human_miRNA_ID_2794950,Human_miRNA_ID_2794951,Human_miRNA_ID_2795417,Human_miRNA_ID_2795418 RMVar_hsa_circ_82556,RMVar_hsa_circ_95101,RMVar_hsa_circ_124982,RMVar_hsa_circ_181741,RMVar_hsa_circ_181742,RMVar_hsa_circ_181743 104240 RMVar_ID_104240 Human_SNP_ID_616328710 m1A Human chr17 + 7174952 7174952 7174952 CACACCCTAACCCACATACACAAAACACACCCACAGACACACAACACACCCTTACACACACATAC CACACCCTAACCCACATACACAAAACACACCCGCAGACACACAACACACCCTTACACACACATAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7174943..7175303 26863196 MeRIP-seq:(Medium) rs552542200 Functional Loss SNV dbSNP153 33..33 33 - - - 104241 RMVar_ID_104241 Human_SNP_ID_616328931 m1A Human chr17 + 7175377 7175374 7175378 CACACACACACACAACACACCCTCACCCAAACACACACAAAAACCACAACACACCCTCACACAGG CACACACACACACAACACACCCTCACCCAA____ACACAAAAACCACAACACACCCTCACACAGG AACAC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7175375..7175524 26863196 MeRIP-seq:(Medium) rs920584060 Functional Loss DEL dbSNP153 31..34 33 - - - 104242 RMVar_ID_104242 Human_SNP_ID_616328932 m1A Human chr17 + 7175377 7175374 7175378 CACACACACACACAACACACCCTCACCCAAACACACACAAAAACCACAACACACCCTCACACAGG CACACACACACACAACACACCCTCACCCAAAC__ACACAAAAACCACAACACACCCTCACACAGG AACAC AAC - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7175375..7175524 26863196 MeRIP-seq:(Medium) rs920584060 Functional Loss DEL dbSNP153 33..34 33 - - - 104243 RMVar_ID_104243 Human_SNP_ID_616328933 m1A Human chr17 + 7175377 7175377 7175377 CACACACACACACAACACACCCTCACCCAAACACACACAAAAACCACAACACACCCTCACACAGG CACACACACACACAACACACCCTCACCCAAACTCACACAAAAACCACAACACACCCTCACACAGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7175375..7175524 26863196 MeRIP-seq:(Medium) rs1475364185 Functional Loss SNV dbSNP153 33..33 33 - - - 104244 RMVar_ID_104244 Human_SNP_ID_616329284 m1A Human chr17 - 7175925 7175923 7175925 GTTAGTGTGTGTTGCGTGTGTGGGGGAATGAGAGGGATTGTGTCTGTGAGTGTGAGAATGAGATG GTTAGTGTGTGTTGCGTGTGTGGGGGAATGAG__GGATTGTGTCTGTGAGTGTGAGAATGAGATG CCT C ASGR1 Ensembl:ENSG00000141505 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7175923..7176037 26863196 MeRIP-seq:(Medium) rs370750138 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_498690,Human_RBP_ID_3542555,Human_RBP_ID_5289974,Human_RBP_ID_5648393,Human_RBP_ID_8191718,Human_RBP_ID_17263519,Human_RBP_ID_23114211,Human_RBP_ID_23276413 RMVar_hsa_circ_377236 104245 RMVar_ID_104245 Human_SNP_ID_616329428 m1A Human chr17 - 7176118 7176114 7176118 GAATGAGATGGGTGTGTGTGTGACAGAGTCTGAGTGTGAGAATGAGAGGGAGTGTGTGTGAGTGT GAATGAGATGGGTGTGTGTGTGACAGAGTCTG____TGAGAATGAGAGGGAGTGTGTGTGAGTGT ACACT A ASGR1 Ensembl:ENSG00000141505 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7176116..7176198 26863196 MeRIP-seq:(Medium) rs1253028599 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5290515,Human_RBP_ID_5648395,Human_RBP_ID_17263816,Human_RBP_ID_23114213 RMVar_hsa_circ_377236 104246 RMVar_ID_104246 Human_SNP_ID_616329429 m1A Human chr17 - 7176118 7176116 7176118 GAATGAGATGGGTGTGTGTGTGACAGAGTCTGAGTGTGAGAATGAGAGGGAGTGTGTGTGAGTGT GAATGAGATGGGTGTGTGTGTGACAGAGTCTG__TGTGAGAATGAGAGGGAGTGTGTGTGAGTGT ACT A ASGR1 Ensembl:ENSG00000141505 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7176116..7176198 26863196 MeRIP-seq:(Medium) rs577151897 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5290515,Human_RBP_ID_5648395,Human_RBP_ID_17263816,Human_RBP_ID_23114213 RMVar_hsa_circ_377236 104247 RMVar_ID_104247 Human_SNP_ID_616329680 m1A Human chr17 + 7176413 7176411 7176413 CTCAGACTCACACACACCTCATTATCACACTCACAGACACACTCCGTCATTCTCACACTCTCACA CTCAGACTCACACACACCTCATTATCACACT__CAGACACACTCCGTCATTCTCACACTCTCACA TCA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7176406..7176516 26863196 MeRIP-seq:(Medium) rs754049885 Functional Loss DEL dbSNP153 32..33 33 - - - 104248 RMVar_ID_104248 Human_SNP_ID_616329684 m1A Human chr17 + 7176413 7176412 7176413 CTCAGACTCACACACACCTCATTATCACACTCACAGACACACTCCGTCATTCTCACACTCTCACA CTCAGACTCACACACACCTCATTATCACACTC_CAGACACACTCCGTCATTCTCACACTCTCACA CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7176406..7176516 26863196 MeRIP-seq:(Medium) rs1414009678 Functional Loss DEL dbSNP153 33..33 33 - - - 104249 RMVar_ID_104249 Human_SNP_ID_616329801 m1A Human chr17 - 7176564 7176538 7176564 ATGGAGTGTGTGTGAGTCTGTGTGTGAGAATGAGGTGTGTGTGTGTGAGAATGAGATGGTGTGTG ATGGAGTGTGTGTGAGTCTGTGTGTGAGAATG__________________________GTGTGTG CCATCTCATTCTCACACACACACACCT C ASGR1 Ensembl:ENSG00000141505 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7176562..7176660 26863196 MeRIP-seq:(Medium) rs778137140 Functional Loss DEL dbSNP153 33..58 33 - - - Human_RBP_ID_5289982,Human_RBP_ID_23114217,Human_RBP_ID_23747152 RMVar_hsa_circ_377236 104250 RMVar_ID_104250 Human_SNP_ID_616329840 m1A Human chr17 + 7176590 7176590 7176590 CACACCTCATTCTCACACACAGACTCACACACACTCCATCTCATTCTCACACTCACAGACATACA CACACCTCATTCTCACACACAGACTCACACACCCTCCATCTCATTCTCACACTCACAGACATACA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7176586..7176675 26863196 MeRIP-seq:(Medium) rs745683926 Functional Loss SNV dbSNP153 33..33 33 - - - 104251 RMVar_ID_104251 Human_SNP_ID_616334748 m1A Human chr17 + 7192102 7192102 7192102 AGGGACACGGACGGGGAGAGGTGGGGAATGGGAAGTTGGCCGAAGGGGAGTGACATGGATGTCAA AGGGACACGGACGGGGAGAGGTGGGGAATGGGCAGTTGGCCGAAGGGGAGTGACATGGATGTCAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7192091..7192341 26863196 MeRIP-seq:(Medium) rs1293381080 Functional Loss SNV dbSNP153 33..33 33 - - - 104252 RMVar_ID_104252 Human_SNP_ID_616334963 m1A Human chr17 + 7192936 7192936 7192936 GAGGGGAGAAGGAAGAGGACCGGGTGCCCGCCAGGTCCTACCTGCTCTGCCACCTCTCGCACGGA GAGGGGAGAAGGAAGAGGACCGGGTGCCCGCCGGGTCCTACCTGCTCTGCCACCTCTCGCACGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7192931..7193002 26863196 MeRIP-seq:(Medium) rs1431426187 Functional Loss SNV dbSNP153 33..33 33 - - - 104253 RMVar_ID_104253 Human_SNP_ID_616334967 m1A Human chr17 - 7192951 7192951 7192951 GGGACCAGCGTCCAGTCCGTGCGAGAGGTGGCAGAGCAGGTAGGACCTGGCGGGCACCCGGTCCT GGGACCAGCGTCCAGTCCGTGCGAGAGGTGGCGGAGCAGGTAGGACCTGGCGGGCACCCGGTCCT T C DLG4 Ensembl:ENSG00000132535 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7192923..7192994 26863196 MeRIP-seq:(Medium) rs1371448069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1769335,Human_Splice_Rec_1769375,Human_Splice_Rec_1769417,Human_Splice_Rec_1769457,Human_Splice_Rec_1769491,Human_Splice_Rec_1769531,Human_Splice_Rec_1769565,Human_Splice_Rec_1769599,Human_Splice_Rec_1769635,Human_Splice_Rec_1769675,Human_Splice_Rec_1769695,Human_Splice_Rec_1769731 RMVar_hsa_circ_266955 104254 RMVar_ID_104254 Human_SNP_ID_616336140 m1A Human chr17 - 7197002 7197002 7197002 ACAATGAGATCAGTCACAGCAGCTACCTGGGCACCGACTACCCCACAGCCATGACCCCCACTTCC ACAATGAGATCAGTCACAGCAGCTACCTGGGCGCCGACTACCCCACAGCCATGACCCCCACTTCC T C DLG4 Ensembl:ENSG00000132535 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7196952..7197035 26863196 MeRIP-seq:(Medium) rs370645685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18707753 Human_Splice_Rec_1769318,Human_Splice_Rec_1769358,Human_Splice_Rec_1769400,Human_Splice_Rec_1769440,Human_Splice_Rec_1769474,Human_Splice_Rec_1769514,Human_Splice_Rec_1769548,Human_Splice_Rec_1769582,Human_Splice_Rec_1769618,Human_Splice_Rec_1769658,Human_Splice_Rec_1769714,Human_Splice_Rec_1769742,Human_Splice_Rec_1769768 RMVar_hsa_circ_20200,RMVar_hsa_circ_266955,RMVar_hsa_circ_17409,RMVar_hsa_circ_15414,RMVar_hsa_circ_181751 104255 RMVar_ID_104255 Human_SNP_ID_616337683 m1A Human chr17 - 7203041 7203041 7203041 CTGAGCTTTGCTTTCCTTGACTCCAGGTCAACAGTGTGGGGCTAGAGGACGTCATGCATGAAGAT CTGAGCTTTGCTTTCCTTGACTCCAGGTCAACTGTGTGGGGCTAGAGGACGTCATGCATGAAGAT T A DLG4 Ensembl:ENSG00000132535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7202991..7203581 32194978 MeRIP-seq:(Medium) rs758618486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3951729,Human_RBP_ID_26331161 Human_Splice_Rec_1769316,Human_Splice_Rec_1769356,Human_Splice_Rec_1769398,Human_Splice_Rec_1769438,Human_Splice_Rec_1769472,Human_Splice_Rec_1769512,Human_Splice_Rec_1769546,Human_Splice_Rec_1769580,Human_Splice_Rec_1769616,Human_Splice_Rec_1769656,Human_Splice_Rec_1769712,Human_Splice_Rec_1769740,Human_Splice_Rec_1769766,Human_Splice_Rec_1769782,Human_Splice_Rec_1769792,Human_Splice_Rec_1769802,Human_Splice_Rec_1769814 RMVar_hsa_circ_266955,RMVar_hsa_circ_15414,RMVar_hsa_circ_181751 104256 RMVar_ID_104256 Human_SNP_ID_616338497 m1A Human chr17 + 7205821 7205803 7205822 CGTCCCCCATCCCGCAGCCCGTCCTCCATCCCATAGCCCGTCCTCCATCCCATAGCCCATCCTCA CGTCCCCCATCCCGC___________________AGCCCGTCCTCCATCCCATAGCCCATCCTCA CAGCCCGTCCTCCATCCCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7205818..7206044 26863196 MeRIP-seq:(Medium) rs1303146144 Functional Loss DEL dbSNP153 16..34 33 - - - 104257 RMVar_ID_104257 Human_SNP_ID_616338502 m1A Human chr17 + 7205821 7205821 7205822 CGTCCCCCATCCCGCAGCCCGTCCTCCATCCCATAGCCCGTCCTCCATCCCATAGCCCATCCTCA CGTCCCCCATCCCGCAGCCCGTCCTCCATCCCGCAGCCCGTCCTCCATCCCATAGCCCATCCTCA AT GC - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7205818..7206044 26863196 MeRIP-seq:(Medium) rs386795010 Functional Loss MNV dbSNP153 33..34 33 - - - 104258 RMVar_ID_104258 Human_SNP_ID_616338503 m1A Human chr17 + 7205821 7205821 7205821 CGTCCCCCATCCCGCAGCCCGTCCTCCATCCCATAGCCCGTCCTCCATCCCATAGCCCATCCTCA CGTCCCCCATCCCGCAGCCCGTCCTCCATCCCGTAGCCCGTCCTCCATCCCATAGCCCATCCTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7205818..7206044 26863196 MeRIP-seq:(Medium) rs1031788581 Functional Loss SNV dbSNP153 33..33 33 - - - 104259 RMVar_ID_104259 Human_SNP_ID_616338659 m1A Human chr17 - 7206583 7206571 7206583 CTGTGGATGCTAGGAGTGAGGGAAAGAAGACTAGAGATGCTTTGTGCAAGGCAGGGCCATTAAAT CTGTGGATGCTAGGAGTGAGGGAAAGAAGACT____________TGCAAGGCAGGGCCATTAAAT ACAAAGCATCTCT A DLG4 Ensembl:ENSG00000132535 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7206581..7206796 26863196 MeRIP-seq:(Medium) rs1206990521 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_23747384 RMVar_hsa_circ_266955 104260 RMVar_ID_104260 Human_SNP_ID_616338666 m1A Human chr17 - 7206583 7206583 7206583 CTGTGGATGCTAGGAGTGAGGGAAAGAAGACTAGAGATGCTTTGTGCAAGGCAGGGCCATTAAAT CTGTGGATGCTAGGAGTGAGGGAAAGAAGACTTGAGATGCTTTGTGCAAGGCAGGGCCATTAAAT T A DLG4 Ensembl:ENSG00000132535 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7206581..7206796 26863196 MeRIP-seq:(Medium) rs1429529784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23747384 RMVar_hsa_circ_266955 104261 RMVar_ID_104261 Human_SNP_ID_616341471 m1A Human chr17 + 7217554 7217554 7217554 AAACGGCCAGGGGCTAGGGGCCGTGGCGGGGGAGTGGGGTGGGGGGGTTGGAAACGGCAGCGGCC AAACGGCCAGGGGCTAGGGGCCGTGGCGGGGGGGTGGGGTGGGGGGGTTGGAAACGGCAGCGGCC A G ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7217323..7217600 26863196 MeRIP-seq:(Medium) rs917128842 Functional Loss SNV dbSNP153 33..33 33 - - - 104262 RMVar_ID_104262 Human_SNP_ID_616342246 m1A Human chr17 + 7219938 7219936 7219938 AGGGGCGCCAGGACGTGGGCGTGCAGGACGCCAGAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC AGGGGCGCCAGGACGTGGGCGTGCAGGACGC__GAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC CCA C ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:7219876..7220230;chr17:7219876..7220259 26863196 MeRIP-seq:(Medium) rs1491200783 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_819875,Human_RBP_ID_4465114,Human_RBP_ID_8727030,Human_RBP_ID_18419847,Human_RBP_ID_22426269 104263 RMVar_ID_104263 Human_SNP_ID_616342253 m1A Human chr17 + 7219938 7219937 7219938 AGGGGCGCCAGGACGTGGGCGTGCAGGACGCCAGAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC AGGGGCGCCAGGACGTGGGCGTGCAGGACGCGGGAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC CA GG ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:7219876..7220230;chr17:7219876..7220259 26863196 MeRIP-seq:(Medium) rs867758455 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_819875,Human_RBP_ID_4465114,Human_RBP_ID_8727030,Human_RBP_ID_18419847,Human_RBP_ID_22426269 104264 RMVar_ID_104264 Human_SNP_ID_616342254 m1A Human chr17 + 7219938 7219938 7219938 AGGGGCGCCAGGACGTGGGCGTGCAGGACGCCAGAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC AGGGGCGCCAGGACGTGGGCGTGCAGGACGCCGGAGCTGGGTCAGAGCTCGAGCCAGCGGCGCCC A G ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:7219876..7220230;chr17:7219876..7220259 26863196 MeRIP-seq:(Medium) rs763375468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819875,Human_RBP_ID_4465114,Human_RBP_ID_8727030,Human_RBP_ID_18419847,Human_RBP_ID_22426269 104265 RMVar_ID_104265 Human_SNP_ID_616342291 m1A Human chr17 - 7220013 7219997 7220014 TTCCGCCCCCGAGCCTCAGCAGCTGCCGCCCCAAGCTCGCGGCCATCCGAGCCGCCTGCATCTCC TTCCGCCCCCGAGCCTCAGCAGCTGCCGCCC_________________GAGCCGCCTGCATCTCC CGGATGGCCGCGAGCTTG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7219946..7220101 26863196 MeRIP-seq:(Medium) rs1555527450 Functional Loss DEL dbSNP153 32..48 33 - - - Clinvar_Rec_648 104266 RMVar_ID_104266 Human_SNP_ID_616342309 m1A Human chr17 + 7220030 7220030 7220030 GGATGGCCGCGAGCTTGGGGCGGCAGCTGCTGAGGCTCGGGGGCGGAAGGTCTGTGTGTGACAAG GGATGGCCGCGAGCTTGGGGCGGCAGCTGCTGGGGCTCGGGGGCGGAAGGTCTGTGTGTGACAAG A G ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7219901..7220155 26863196 MeRIP-seq:(Medium) rs763471070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237525,Human_RBP_ID_498783,Human_RBP_ID_819876,Human_RBP_ID_899248,Human_RBP_ID_4464287,Human_RBP_ID_8825255,Human_RBP_ID_9288691,Human_RBP_ID_18419849,Human_RBP_ID_18469962,Human_RBP_ID_18987773,Human_RBP_ID_22443418,Human_RBP_ID_22585201,Human_RBP_ID_22740476,Human_RBP_ID_23209797 Human_Splice_Rec_1769911,Human_Splice_Rec_1769917,Human_Splice_Rec_1769931,Human_Splice_Rec_1769965,Human_Splice_Rec_1769967,Human_Splice_Rec_1769979,Human_Splice_Rec_1769983,Human_Splice_Rec_1769991,Human_Splice_Rec_1769999,Human_Splice_Rec_1770009,Human_Splice_Rec_1770025,Human_Splice_Rec_1770037,Human_Splice_Rec_1770073 104267 RMVar_ID_104267 Human_SNP_ID_616342402 m1A Human chr17 - 7220177 7220177 7220177 GCGGTGACTTACCTGAGCGGCACCCCCGGCATAGGGCCGCCGGGCAGGGCCGGGCCGGGGCTGCC GCGGTGACTTACCTGAGCGGCACCCCCGGCATGGGGCCGCCGGGCAGGGCCGGGCCGGGGCTGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7219976..7220299 32194978 MeRIP-seq:(Medium) rs1430338838 Functional Loss SNV dbSNP153 33..33 33 - - - 104268 RMVar_ID_104268 Human_SNP_ID_616342565 m1A Human chr17 + 7220559 7220559 7220559 GCGGTAGGTAGCCCCGAGGCCAGGTGGACCTTAGCCAGACCCAACCAGAGCCCTGAAATTTGCCT GCGGTAGGTAGCCCCGAGGCCAGGTGGACCTTGGCCAGACCCAACCAGAGCCCTGAAATTTGCCT A G ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7220551..7220625 26863196 MeRIP-seq:(Medium) rs1321805441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2522067,Human_RBP_ID_18707847,Human_RBP_ID_19078193,Human_RBP_ID_22357698,Human_RBP_ID_22415868,Human_RBP_ID_22542853,Human_RBP_ID_22655747,Human_RBP_ID_22740181,Human_RBP_ID_26781960 Human_Splice_Rec_1769844,Human_Splice_Rec_1769878,Human_Splice_Rec_1769914,Human_Splice_Rec_1769920,Human_Splice_Rec_1769970,Human_Splice_Rec_1769982,Human_Splice_Rec_1769986,Human_Splice_Rec_1770002,Human_Splice_Rec_1770012,Human_Splice_Rec_1770024,Human_Splice_Rec_1770028,Human_Splice_Rec_1770040,Human_Splice_Rec_1770076 RMVar_hsa_circ_119969,RMVar_hsa_circ_181753 104269 RMVar_ID_104269 Human_SNP_ID_616342707 m1A Human chr17 - 7220826 7220817 7220826 AGGGACCAAGCCCCGAGTCATTCCTTACCTCGAAGAAACGGGACACAGGCTCCACCAGCTCTTTA AGGGACCAAGCCCCGAGTCATTCCTTACCTCG_________GACACAGGCTCCACCAGCTCTTTA CCCGTTTCTT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7220776..7220850 32194978 MeRIP-seq:(Medium) rs1555527820 Functional Loss DEL dbSNP153 33..41 33 - - - Clinvar_Rec_649 104270 RMVar_ID_104270 Human_SNP_ID_616342711 m1A Human chr17 - 7220821 7220820 7220821 CCAAGCCCCGAGTCATTCCTTACCTCGAAGAAACGGGACACAGGCTCCACCAGCTCTTTAAGAAA CCAAGCCCCGAGTCATTCCTTACCTCGAAGAA_CGGGACACAGGCTCCACCAGCTCTTTAAGAAA GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7220751..7220850 32194978 MeRIP-seq:(Medium) rs764028320 Functional Loss DEL dbSNP153 33..33 33 - - - 104271 RMVar_ID_104271 Human_SNP_ID_616342799 m1A Human chr17 + 7220967 7220964 7220967 TCCCGCCAAGAATGACGCTCTGGAGATGGTGGAGGAGACCACTTGGCAGGGCCTCAAGGAGCTGG TCCCGCCAAGAATGACGCTCTGGAGATGGT___GGAGACCACTTGGCAGGGCCTCAAGGAGCTGG TGGA T ACADVL Ensembl:ENSG00000072778 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7220951..7220975 26863196 MeRIP-seq:(Medium) rs387906251 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_819095,Human_RBP_ID_899250,Human_RBP_ID_3951733,Human_RBP_ID_13154014,Human_RBP_ID_17905682,Human_RBP_ID_18191169,Human_RBP_ID_18987777,Human_RBP_ID_22220280,Human_RBP_ID_27812220 Human_Splice_Rec_1769850,Human_Splice_Rec_1769851,Human_Splice_Rec_1769884,Human_Splice_Rec_1769885,Human_Splice_Rec_1769926,Human_Splice_Rec_1769927,Human_Splice_Rec_1769938,Human_Splice_Rec_1769939,Human_Splice_Rec_1769974,Human_Splice_Rec_1769975,Human_Splice_Rec_1770008,Human_Splice_Rec_1770018,Human_Splice_Rec_1770019,Human_Splice_Rec_1770034,Human_Splice_Rec_1770035,Human_Splice_Rec_1770046,Human_Splice_Rec_1770047,Human_Splice_Rec_1770077,Human_Splice_Rec_1770084,Human_Splice_Rec_1770085,Human_Splice_Rec_1770091,Human_Splice_Rec_1770094,Human_Splice_Rec_1770095,Human_Splice_Rec_1770100,Human_Splice_Rec_1770101 Human_miRNA_ID_864795,Human_miRNA_ID_2381293,Human_miRNA_ID_3024302 Clinvar_Rec_650 RMVar_hsa_circ_104346,RMVar_hsa_circ_119969,RMVar_hsa_circ_374454,RMVar_hsa_circ_181753,RMVar_hsa_circ_181754,RMVar_hsa_circ_181756 104272 RMVar_ID_104272 Human_SNP_ID_616342802 m1A Human chr17 + 7220967 7220967 7220967 TCCCGCCAAGAATGACGCTCTGGAGATGGTGGAGGAGACCACTTGGCAGGGCCTCAAGGAGCTGG TCCCGCCAAGAATGACGCTCTGGAGATGGTGGTGGAGACCACTTGGCAGGGCCTCAAGGAGCTGG A T ACADVL Ensembl:ENSG00000072778 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7220951..7220975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_819095,Human_RBP_ID_899250,Human_RBP_ID_3951733,Human_RBP_ID_13154014,Human_RBP_ID_17905682,Human_RBP_ID_18191169,Human_RBP_ID_18987777,Human_RBP_ID_22220280,Human_RBP_ID_27812220 Human_Splice_Rec_1769850,Human_Splice_Rec_1769851,Human_Splice_Rec_1769884,Human_Splice_Rec_1769885,Human_Splice_Rec_1769926,Human_Splice_Rec_1769927,Human_Splice_Rec_1769938,Human_Splice_Rec_1769939,Human_Splice_Rec_1769974,Human_Splice_Rec_1769975,Human_Splice_Rec_1770008,Human_Splice_Rec_1770018,Human_Splice_Rec_1770019,Human_Splice_Rec_1770034,Human_Splice_Rec_1770035,Human_Splice_Rec_1770046,Human_Splice_Rec_1770047,Human_Splice_Rec_1770077,Human_Splice_Rec_1770084,Human_Splice_Rec_1770085,Human_Splice_Rec_1770091,Human_Splice_Rec_1770094,Human_Splice_Rec_1770095,Human_Splice_Rec_1770100,Human_Splice_Rec_1770101 Human_miRNA_ID_864795,Human_miRNA_ID_2381293,Human_miRNA_ID_3024302 RMVar_hsa_circ_104346,RMVar_hsa_circ_119969,RMVar_hsa_circ_374454,RMVar_hsa_circ_181753,RMVar_hsa_circ_181754,RMVar_hsa_circ_181756 104273 RMVar_ID_104273 Human_SNP_ID_616343118 m1A Human chr17 - 7221679 7221679 7221679 AATCCCTGGCTCTCCTAGGGTTGCCTCACCAGATGCCAGCTTGGGGAGGTATTTTTCTTTCTGGG AATCCCTGGCTCTCCTAGGGTTGCCTCACCAGGTGCCAGCTTGGGGAGGTATTTTTCTTTCTGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7221498..7221709 26863196 MeRIP-seq:(Medium) rs768975918 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_651 104274 RMVar_ID_104274 Human_SNP_ID_616343119 m1A Human chr17 - 7221679 7221679 7221679 AATCCCTGGCTCTCCTAGGGTTGCCTCACCAGATGCCAGCTTGGGGAGGTATTTTTCTTTCTGGG AATCCCTGGCTCTCCTAGGGTTGCCTCACCAGCTGCCAGCTTGGGGAGGTATTTTTCTTTCTGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7221498..7221709 26863196 MeRIP-seq:(Medium) rs768975918 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_651 104275 RMVar_ID_104275 Human_SNP_ID_616343371 m1A Human chr17 - 7222272 7222272 7222272 ACTGGGTAATGCCCCCGAAGCCCCTCTCCACCACAAAAGCTGTGATCTTCTCCTTCACGGCTCCT ACTGGGTAATGCCCCCGAAGCCCCTCTCCACCGCAAAAGCTGTGATCTTCTCCTTCACGGCTCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7221954..7222323 26863196 MeRIP-seq:(Medium) rs113994167 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_652 GWAS_ID_13592 104276 RMVar_ID_104276 Human_SNP_ID_616343583 m1A Human chr17 - 7222766 7222766 7222766 AGGATGTGCATGGCAACCTTGAAGCCACTCCCAACCTCACCCAGCACGTTCTCCGATGGCACCCG AGGATGTGCATGGCAACCTTGAAGCCACTCCCGACCTCACCCAGCACGTTCTCCGATGGCACCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7222639..7223255 26863196 MeRIP-seq:(Medium) rs1250294445 Functional Loss SNV dbSNP153 33..33 33 - - - 104277 RMVar_ID_104277 Human_SNP_ID_616343584 m1A Human chr17 - 7222766 7222766 7222766 AGGATGTGCATGGCAACCTTGAAGCCACTCCCAACCTCACCCAGCACGTTCTCCGATGGCACCCG AGGATGTGCATGGCAACCTTGAAGCCACTCCCTACCTCACCCAGCACGTTCTCCGATGGCACCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7222639..7223255 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 104278 RMVar_ID_104278 Human_SNP_ID_616343588 m1A Human chr17 - 7222772 7222772 7222772 TTGTTGAGGATGTGCATGGCAACCTTGAAGCCACTCCCAACCTCACCCAGCACGTTCTCCGATGG TTGTTGAGGATGTGCATGGCAACCTTGAAGCCGCTCCCAACCTCACCCAGCACGTTCTCCGATGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7222651..7222825 32194978 MeRIP-seq:(Medium) rs148803927 Functional Loss SNV dbSNP153 33..33 33 - - - 104279 RMVar_ID_104279 Human_SNP_ID_616343952 m1A Human chr17 + 7223628 7223628 7223628 AAAGCCCTTTGCAATTTTCCTTCCCATGTCCCAACTATGCAACCTCAGTCCATGGCTTACATGGT AAAGCCCTTTGCAATTTTCCTTCCCATGTCCCCACTATGCAACCTCAGTCCATGGCTTACATGGT A C ACADVL Ensembl:ENSG00000072778 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7223626..7223675 26863196 MeRIP-seq:(Medium) rs1319240451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22655752,Human_RBP_ID_25336655 RMVar_hsa_circ_104346,RMVar_hsa_circ_119969,RMVar_hsa_circ_181753,RMVar_hsa_circ_15502,RMVar_hsa_circ_181756 104280 RMVar_ID_104280 Human_SNP_ID_616344146 m1A Human chr17 - 7224071 7224071 7224071 CCCACCTCTACCCCCACCCAATTCTCTGTCTTACCATACAGCCCTGCAGAGCCACAAACAGCCGA CCCACCTCTACCCCCACCCAATTCTCTGTCTTCCCATACAGCCCTGCAGAGCCACAAACAGCCGA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7223951..7224075 32194978 MeRIP-seq:(Medium) rs1555528804 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_653 104281 RMVar_ID_104281 Human_SNP_ID_616344221 m1A Human chr17 + 7224226 7224226 7224226 TTTGGGAATGCTGGCCTCCTGCTAGGAGAGGCAGGCAAACAGCTGAGGCGGTAGGCTTAGGGCCA TTTGGGAATGCTGGCCTCCTGCTAGGAGAGGCCGGCAAACAGCTGAGGCGGTAGGCTTAGGGCCA A C ACADVL Ensembl:ENSG00000072778 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7224201..7224225 26863196 MeRIP-seq:(Medium) rs781153542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235703,Human_RBP_ID_764449,Human_RBP_ID_819438,Human_RBP_ID_899265,Human_RBP_ID_3950031,Human_RBP_ID_18163880,Human_RBP_ID_18469971,Human_RBP_ID_18987793,Human_RBP_ID_22443421 Human_Splice_Rec_1769866,Human_Splice_Rec_1769867,Human_Splice_Rec_1769900,Human_Splice_Rec_1769901,Human_Splice_Rec_1769954,Human_Splice_Rec_1769955,Human_Splice_Rec_1770062,Human_Splice_Rec_1770063,Human_Splice_Rec_1770140,Human_Splice_Rec_1770141,Human_Splice_Rec_1770154,Human_Splice_Rec_1770155,Human_Splice_Rec_1770176,Human_Splice_Rec_1770177,Human_Splice_Rec_1770206,Human_Splice_Rec_1770207,Human_Splice_Rec_1770225,Human_Splice_Rec_1770229,Human_Splice_Rec_1770241 RMVar_hsa_circ_104346,RMVar_hsa_circ_119969,RMVar_hsa_circ_181753,RMVar_hsa_circ_15502,RMVar_hsa_circ_181756,RMVar_hsa_circ_124439,RMVar_hsa_circ_114425,RMVar_hsa_circ_181758,RMVar_hsa_circ_104722,RMVar_hsa_circ_181759,RMVar_hsa_circ_181760,RMVar_hsa_circ_30443,RMVar_hsa_circ_365360 104282 RMVar_ID_104282 Human_SNP_ID_616344233 m1A Human chr17 - 7224245 7224245 7224245 CCCTGCCCTCCCCTGGCTCTGGCCCTAAGCCTACCGCCTCAGCTGTTTGCCTGCCTCTCCTAGCA CCCTGCCCTCCCCTGGCTCTGGCCCTAAGCCTTCCGCCTCAGCTGTTTGCCTGCCTCTCCTAGCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7224126..7224400 32194978 MeRIP-seq:(Medium) rs111851815 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_654 104283 RMVar_ID_104283 Human_SNP_ID_616344234 m1A Human chr17 - 7224245 7224245 7224245 CCCTGCCCTCCCCTGGCTCTGGCCCTAAGCCTACCGCCTCAGCTGTTTGCCTGCCTCTCCTAGCA CCCTGCCCTCCCCTGGCTCTGGCCCTAAGCCTGCCGCCTCAGCTGTTTGCCTGCCTCTCCTAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7224126..7224400 32194978 MeRIP-seq:(Medium) rs111851815 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_654 104284 RMVar_ID_104284 Human_SNP_ID_616345070 m1A Human chr17 - 7226266 7226266 7226266 GGTCGACACGGAGTGATGGGGGGGCAGGGCGCACGGGGAGGCCCGAGGAGCGGGCCCCCGAGTCC GGTCGACACGGAGTGATGGGGGGGCAGGGCGCGCGGGGAGGCCCGAGGAGCGGGCCCCCGAGTCC T C DVL2 Ensembl:ENSG00000004975 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7225948..7226265 26863196 MeRIP-seq:(Medium) rs1432128654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235481,Human_RBP_ID_764184,Human_RBP_ID_819126,Human_RBP_ID_8232284,Human_RBP_ID_8462310,Human_RBP_ID_13154297,Human_RBP_ID_18990320 Human_Splice_Rec_1770286,Human_Splice_Rec_1770314,Human_Splice_Rec_1770326 RMVar_hsa_circ_80217,RMVar_hsa_circ_181765 104285 RMVar_ID_104285 Human_SNP_ID_616345270 m1A Human chr17 - 7226716 7226716 7226716 CCATCGTGGGTGGGTCTGGGAGAACTGTTCCCAGTTCCTCTCCATTCGGTGTCTTGGGGCCCTAG CCATCGTGGGTGGGTCTGGGAGAACTGTTCCCGGTTCCTCTCCATTCGGTGTCTTGGGGCCCTAG T C DVL2 Ensembl:ENSG00000004975 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7226713..7226814 32194978 MeRIP-seq:(Medium) rs972749353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80217,RMVar_hsa_circ_181765 104286 RMVar_ID_104286 Human_SNP_ID_616346337 m1A Human chr17 + 7229541 7229541 7229541 CCGGTGTCCTGGCACCGCCCAAACCAAAGCCCATGCCCCACCTTCTCCCAGCACCAGCCTTCCTG CCGGTGTCCTGGCACCGCCCAAACCAAAGCCCCTGCCCCACCTTCTCCCAGCACCAGCCTTCCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7229535..7229683 26863196 MeRIP-seq:(Medium) rs766165226 Functional Loss SNV dbSNP153 33..33 33 - - - 104287 RMVar_ID_104287 Human_SNP_ID_616346376 m1A Human chr17 + 7229637 7229637 7229637 GCCTCTGCTTCCTTCGCCGCCGGTGGCGCTTAAGGAGGCGGGAGGCACTGCTCTGCTCCGTGGAG GCCTCTGCTTCCTTCGCCGCCGGTGGCGCTTATGGAGGCGGGAGGCACTGCTCTGCTCCGTGGAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7229588..7229674 26863196 MeRIP-seq:(Medium) rs1208017156 Functional Loss SNV dbSNP153 33..33 33 - - - 104288 RMVar_ID_104288 Human_SNP_ID_616346415 m1A Human chr17 + 7229742 7229742 7229742 AGGCCAAAGTGGTCATGGGGCCAAGAGAAAGAACAAGAGGATTGACTGGAAGACGAGACGGGGCT AGGCCAAAGTGGTCATGGGGCCAAGAGAAAGACCAAGAGGATTGACTGGAAGACGAGACGGGGCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7229735..7229820 26863196 MeRIP-seq:(Medium) rs756349052 Functional Loss SNV dbSNP153 33..33 33 - - - 104289 RMVar_ID_104289 Human_SNP_ID_616346416 m1A Human chr17 + 7229742 7229742 7229742 AGGCCAAAGTGGTCATGGGGCCAAGAGAAAGAACAAGAGGATTGACTGGAAGACGAGACGGGGCT AGGCCAAAGTGGTCATGGGGCCAAGAGAAAGAGCAAGAGGATTGACTGGAAGACGAGACGGGGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7229735..7229820 26863196 MeRIP-seq:(Medium) rs756349052 Functional Loss SNV dbSNP153 33..33 33 - - - 104290 RMVar_ID_104290 Human_SNP_ID_616346618 m1A Human chr17 + 7230149 7230149 7230149 TCAGGCTCCAGATTCTCATGGCTGCTGGACACATTAGGGCTGGACAGGCAGAGATGGTTTCCAAC TCAGGCTCCAGATTCTCATGGCTGCTGGACACGTTAGGGCTGGACAGGCAGAGATGGTTTCCAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7230022..7230177 26863196 MeRIP-seq:(Medium) rs752061018 Functional Loss SNV dbSNP153 33..33 33 - - - 104291 RMVar_ID_104291 Human_SNP_ID_616346681 m1A Human chr17 + 7230289 7230289 7230289 CCTGCAGTCAAGAATCTGAAGGACTCACTGGAAGGATGGAGGCCTTGAGTCCCCAATGCCGCTGG CCTGCAGTCAAGAATCTGAAGGACTCACTGGAGGGATGGAGGCCTTGAGTCCCCAATGCCGCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7230278..7230425 26863196 MeRIP-seq:(Medium) rs765091992 Functional Loss SNV dbSNP153 33..33 33 - - - 104292 RMVar_ID_104292 Human_SNP_ID_616346725 m1A Human chr17 - 7230389 7230389 7230389 TCAGATAATCCCCAACCCGAGATGGCCCCTCCAGTCCATGAGCCTCGGGCAGAACTGGCGCCTCC TCAGATAATCCCCAACCCGAGATGGCCCCTCCGGTCCATGAGCCTCGGGCAGAACTGGCGCCTCC T C DVL2 Ensembl:ENSG00000004975 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7230338..7230452 26863196 MeRIP-seq:(Medium) rs1330746904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18707916 Human_Splice_Rec_1770262,Human_Splice_Rec_1770290,Human_Splice_Rec_1770348,Human_Splice_Rec_1770366,Human_Splice_Rec_1770400,Human_Splice_Rec_1770404 Human_miRNA_ID_1981161,Human_miRNA_ID_1982885 RMVar_hsa_circ_2700,RMVar_hsa_circ_80217,RMVar_hsa_circ_181765,RMVar_hsa_circ_36519,RMVar_hsa_circ_114268,RMVar_hsa_circ_181767 104293 RMVar_ID_104293 Human_SNP_ID_616347980 m1A Human chr17 + 7234236 7234236 7234236 AGGTGGTAAATCACCTTCGTCTCCCCAACCCCACCGCCCCCAGTGCTGCTACCCGCCATGGTCTC AGGTGGTAAATCACCTTCGTCTCCCCAACCCCCCCGCCCCCAGTGCTGCTACCCGCCATGGTCTC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7234176..7234375 26863196 MeRIP-seq:(Medium) rs755860169 Functional Loss SNV dbSNP153 33..33 33 - - - 104294 RMVar_ID_104294 Human_SNP_ID_616348003 m1A Human chr17 - 7234267 7234267 7234267 GGTGGGCGGTGGAGCCCGGGAGCGCGCGGGCGAGACCATGGCGGGTAGCAGCACTGGGGGCGGTG GGTGGGCGGTGGAGCCCGGGAGCGCGCGGGCGGGACCATGGCGGGTAGCAGCACTGGGGGCGGTG T C DVL2 Ensembl:ENSG00000004975 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7234048..7234475 26863196 MeRIP-seq:(Medium) rs766891440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237437,Human_RBP_ID_820033,Human_RBP_ID_3542558,Human_RBP_ID_4448752,Human_RBP_ID_17128064,Human_RBP_ID_22062540 104295 RMVar_ID_104295 Human_SNP_ID_616348809 m1A Human chr17 - 7236254 7236252 7236255 GAATCAAGAAGAGCAAGAAGCGGAAGTTAAAAAAGGCAGAACGGGGGGATAGACTCCCACCTCCT GAATCAAGAAGAGCAAGAAGCGGAAGTTAAA___GGCAGAACGGGGGGATAGACTCCCACCTCCT CTTT C PHF23 Ensembl:ENSG00000040633 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7235951..7237675;chr17:7235951..7236756 26863196 MeRIP-seq:(Medium) rs745356125 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_899282,Human_RBP_ID_9375253,Human_RBP_ID_24544972,Human_RBP_ID_27456420 104296 RMVar_ID_104296 Human_SNP_ID_616348913 m1A Human chr17 + 7236479 7236479 7236479 GGGCCGGGAGGTATGTGTCAGGGATGTGGGGGACAAAGGAGATGCCACTTTGGGCCCATCCAGAT GGGCCGGGAGGTATGTGTCAGGGATGTGGGGGGCAAAGGAGATGCCACTTTGGGCCCATCCAGAT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7236350..7236683 26863196 MeRIP-seq:(Medium) rs965472795 Functional Loss SNV dbSNP153 33..33 33 - - - 104297 RMVar_ID_104297 Human_SNP_ID_616349439 m1A Human chr17 - 7237937 7237937 7237937 GGGTGGGGCGCTGAGGGATCCGAGTAGACTGGAGTCGAGAGAGACCGTGAGTTGGGGGGGCGGGG GGGTGGGGCGCTGAGGGATCCGAGTAGACTGGTGTCGAGAGAGACCGTGAGTTGGGGGGGCGGGG T A PHF23 Ensembl:ENSG00000040633 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7237935..7238227 26863196 MeRIP-seq:(Medium) rs1187354167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819805,Human_RBP_ID_3541470,Human_RBP_ID_5366209,Human_RBP_ID_8190873,Human_RBP_ID_13154643 104298 RMVar_ID_104298 Human_SNP_ID_616349984 m1A Human chr17 + 7239229 7239229 7239229 CTCGCCCGCCCCCCGCCGGCTCAGCGCTCTGCACCGGTCGAGAGCTCACCTTCGGGACTGGGCTC CTCGCCCGCCCCCCGCCGGCTCAGCGCTCTGCGCCGGTCGAGAGCTCACCTTCGGGACTGGGCTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7239226..7239400 26863196 MeRIP-seq:(Medium) rs1205896142 Functional Loss SNV dbSNP153 33..33 33 - - - 104299 RMVar_ID_104299 Human_SNP_ID_616350524 m1A Human chr17 - 7240813 7240810 7240814 CCCCTGAGCTGGAGGGGGGTCTCATTCTACAAAGAGAGAGGTGGCCCCCCTTTCTTGACCTCCTC CCCCTGAGCTGGAGGGGGGTCTCATTCTACA____GAGAGGTGGCCCCCCTTTCTTGACCTCCTC CTCTT C AC120057.2,GABARAP Ensembl:ENSG00000262526,Ensembl:ENSG00000170296 Protein coding,Protein coding 3'UTR,3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1179401503 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_498894,Human_RBP_ID_1010308,Human_RBP_ID_1092334,Human_RBP_ID_5420416,Human_RBP_ID_6641789,Human_RBP_ID_9076089,Human_RBP_ID_17378138,Human_RBP_ID_17692959,Human_RBP_ID_17900313,Human_RBP_ID_18439599 RMVar_hsa_circ_92173,RMVar_hsa_circ_116320,RMVar_hsa_circ_127741,RMVar_hsa_circ_111821,RMVar_hsa_circ_181770,RMVar_hsa_circ_181772,RMVar_hsa_circ_181773,RMVar_hsa_circ_181771 104300 RMVar_ID_104300 Human_SNP_ID_616350525 m1A Human chr17 - 7240813 7240812 7240814 CCCCTGAGCTGGAGGGGGGTCTCATTCTACAAAGAGAGAGGTGGCCCCCCTTTCTTGACCTCCTC CCCCTGAGCTGGAGGGGGGTCTCATTCTACA__GAGAGAGGTGGCCCCCCTTTCTTGACCTCCTC CTT C AC120057.2,GABARAP Ensembl:ENSG00000262526,Ensembl:ENSG00000170296 Protein coding,Protein coding 3'UTR,3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs771424438 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_498894,Human_RBP_ID_1010308,Human_RBP_ID_1092334,Human_RBP_ID_5420416,Human_RBP_ID_6641789,Human_RBP_ID_9076089,Human_RBP_ID_17378138,Human_RBP_ID_17692959,Human_RBP_ID_17900313,Human_RBP_ID_18439599 RMVar_hsa_circ_92173,RMVar_hsa_circ_116320,RMVar_hsa_circ_127741,RMVar_hsa_circ_111821,RMVar_hsa_circ_181770,RMVar_hsa_circ_181772,RMVar_hsa_circ_181773,RMVar_hsa_circ_181771 104301 RMVar_ID_104301 Human_SNP_ID_616350968 m1A Human chr17 + 7242320 7242320 7242320 GGCGCTTCTCGAACGGATGCTCTTCTTTGTACACGAACTTCATCCTCCCGGGAACCGGGCTGGAC GGCGCTTCTCGAACGGATGCTCTTCTTTGTACCCGAACTTCATCCTCCCGGGAACCGGGCTGGAC A C AC120057.3 Ensembl:ENSG00000279641 Other exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7242199..7242438 26863196 MeRIP-seq:(Medium) rs902008937 Functional Loss SNV dbSNP153 33..33 33 - - - 104302 RMVar_ID_104302 Human_SNP_ID_616350976 m1A Human chr17 + 7242340 7242340 7242340 TCTTCTTTGTACACGAACTTCATCCTCCCGGGAACCGGGCTGGACAGGGCTGGGCTGAGGGAACC TCTTCTTTGTACACGAACTTCATCCTCCCGGGCACCGGGCTGGACAGGGCTGGGCTGAGGGAACC A C AC120057.3 Ensembl:ENSG00000279641 Other exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7242226..7242450 26863410 MeRIP-seq:(Medium) rs1298198404 Functional Loss SNV dbSNP153 33..33 33 - - - 104303 RMVar_ID_104303 Human_SNP_ID_616350977 m1A Human chr17 + 7242341 7242341 7242341 CTTCTTTGTACACGAACTTCATCCTCCCGGGAACCGGGCTGGACAGGGCTGGGCTGAGGGAACCC CTTCTTTGTACACGAACTTCATCCTCCCGGGATCCGGGCTGGACAGGGCTGGGCTGAGGGAACCC A T AC120057.3 Ensembl:ENSG00000279641 Other exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7242226..7242433 26863196 MeRIP-seq:(Medium) rs1422553082 Functional Loss SNV dbSNP153 33..33 33 - - - 104304 RMVar_ID_104304 Human_SNP_ID_616350997 m1A Human chr17 + 7242374 7242373 7242374 CCGGGCTGGACAGGGCTGGGCTGAGGGAACCCAGGGGGGCCGGGACGGGGGGCGGCGACGACGGC CCGGGCTGGACAGGGCTGGGCTGAGGGAACCC_GGGGGGCCGGGACGGGGGGCGGCGACGACGGC CA C AC120057.3 Ensembl:ENSG00000279641 Other exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7242193..7242450 26863196 MeRIP-seq:(Medium) rs761744615 Functional Loss DEL dbSNP153 33..33 33 - - - 104305 RMVar_ID_104305 Human_SNP_ID_616352308 m1A Human chr17 - 7246156 7246156 7246156 TGAGGAGAGTATCCTGGAGAGAGGCCTGCTACATGATCCCCTGCCTTCCAGCACTGCACTTTGGA TGAGGAGAGTATCCTGGAGAGAGGCCTGCTACTTGATCCCCTGCCTTCCAGCACTGCACTTTGGA T A CTDNEP1 Ensembl:ENSG00000175826 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7246154..7246238 26863196 MeRIP-seq:(Medium) rs748228830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5361528,Human_RBP_ID_22542872,Human_RBP_ID_22658317,Human_RBP_ID_26781366 RMVar_hsa_circ_16538,RMVar_hsa_circ_181774,RMVar_hsa_circ_112880,RMVar_hsa_circ_367724,RMVar_hsa_circ_114447,RMVar_hsa_circ_181776,RMVar_hsa_circ_347702,RMVar_hsa_circ_181777 104306 RMVar_ID_104306 Human_SNP_ID_616352309 m1A Human chr17 - 7246156 7246156 7246156 TGAGGAGAGTATCCTGGAGAGAGGCCTGCTACATGATCCCCTGCCTTCCAGCACTGCACTTTGGA TGAGGAGAGTATCCTGGAGAGAGGCCTGCTACGTGATCCCCTGCCTTCCAGCACTGCACTTTGGA T C CTDNEP1 Ensembl:ENSG00000175826 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7246154..7246238 26863196 MeRIP-seq:(Medium) rs748228830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5361528,Human_RBP_ID_22542872,Human_RBP_ID_22658317,Human_RBP_ID_26781366 RMVar_hsa_circ_16538,RMVar_hsa_circ_181774,RMVar_hsa_circ_112880,RMVar_hsa_circ_367724,RMVar_hsa_circ_114447,RMVar_hsa_circ_181776,RMVar_hsa_circ_347702,RMVar_hsa_circ_181777 104307 RMVar_ID_104307 Human_SNP_ID_616353930 m1A Human chr17 - 7251501 7251501 7251501 TCCCAGCCCATGTGGGCCCCCGCGGGCTGCCCACGCCTGTCCCCCAGCTCCCCGTTCCGCTGGGC TCCCAGCCCATGTGGGCCCCCGCGGGCTGCCCCCGCCTGTCCCCCAGCTCCCCGTTCCGCTGGGC T G AC003688.2,CTDNEP1 Ensembl:ENSG00000262302,Ensembl:ENSG00000175826 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7251276..7251975 26863196 MeRIP-seq:(Medium) rs1409829658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134175,Human_RBP_ID_498952,Human_RBP_ID_1184078,Human_RBP_ID_3541481,Human_RBP_ID_4448989,Human_RBP_ID_5129041,Human_RBP_ID_5318222,Human_RBP_ID_5441837,Human_RBP_ID_9422754,Human_RBP_ID_17079451,Human_RBP_ID_17565517,Human_RBP_ID_17654530,Human_RBP_ID_18942777 RMVar_hsa_circ_16538 104308 RMVar_ID_104308 Human_SNP_ID_616354024 m1A Human chr17 + 7251751 7251751 7251751 GGCGCGCTAGGGGGCTGCTCGCAGGAACGGGGAGGGCGGGGGCAGCGGCGCGCAAAGGGCCGCGG GGCGCGCTAGGGGGCTGCTCGCAGGAACGGGGGGGGCGGGGGCAGCGGCGCGCAAAGGGCCGCGG A G ELP5 Ensembl:ENSG00000170291 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7251656..7251975 26863410 MeRIP-seq:(Medium) rs919433135 Functional Loss SNV dbSNP153 33..33 33 - - - 104309 RMVar_ID_104309 Human_SNP_ID_616354057 m1A Human chr17 + 7251820 7251819 7251820 GGAGAACGGGCCTGCAGAGCGAAGGAGCAGGGAAGGAGGGGGAGGGGGAGCCGGAGGGCGCAGAG GGAGAACGGGCCTGCAGAGCGAAGGAGCAGGG_AGGAGGGGGAGGGGGAGCCGGAGGGCGCAGAG GA G ELP5 Ensembl:ENSG00000170291 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7251720..7251879 26863196 MeRIP-seq:(Medium) rs139127661 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_13593,GWAS_ID_13594,GWAS_ID_13595,GWAS_ID_13596,GWAS_ID_13597,GWAS_ID_13598,GWAS_ID_13599,GWAS_ID_13600,GWAS_ID_13601,GWAS_ID_13602,GWAS_ID_13603,GWAS_ID_13604,GWAS_ID_13605,GWAS_ID_13606,GWAS_ID_13607,GWAS_ID_13608,GWAS_ID_13609,GWAS_ID_13610,GWAS_ID_13611,GWAS_ID_13612,GWAS_ID_13613,GWAS_ID_13614,GWAS_ID_13615,GWAS_ID_13616,GWAS_ID_13617,GWAS_ID_13618,GWAS_ID_13619,GWAS_ID_13620,GWAS_ID_13621,GWAS_ID_13622,GWAS_ID_13623,GWAS_ID_13624,GWAS_ID_13625,GWAS_ID_13626,GWAS_ID_13627,GWAS_ID_13628,GWAS_ID_13629,GWAS_ID_13630,GWAS_ID_13631,GWAS_ID_13632,GWAS_ID_13633,GWAS_ID_13634,GWAS_ID_13635,GWAS_ID_13636,GWAS_ID_13637,GWAS_ID_13638,GWAS_ID_13639,GWAS_ID_13640,GWAS_ID_13641,GWAS_ID_13642,GWAS_ID_13643,GWAS_ID_13644,GWAS_ID_13645,GWAS_ID_13646,GWAS_ID_13647,GWAS_ID_13648,GWAS_ID_13649,GWAS_ID_13650,GWAS_ID_13651,GWAS_ID_13652,GWAS_ID_13653,GWAS_ID_13654,GWAS_ID_13655,GWAS_ID_13656,GWAS_ID_13657 104310 RMVar_ID_104310 Human_SNP_ID_616354058 m1A Human chr17 + 7251820 7251820 7251820 GGAGAACGGGCCTGCAGAGCGAAGGAGCAGGGAAGGAGGGGGAGGGGGAGCCGGAGGGCGCAGAG GGAGAACGGGCCTGCAGAGCGAAGGAGCAGGGGAGGAGGGGGAGGGGGAGCCGGAGGGCGCAGAG A G ELP5 Ensembl:ENSG00000170291 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7251720..7251879 26863196 MeRIP-seq:(Medium) rs1203523840 Functional Loss SNV dbSNP153 33..33 33 - - - 104311 RMVar_ID_104311 Human_SNP_ID_616354334 m1A Human chr17 - 7252380 7252380 7252380 TGATTATGTTCAATATTCCCAGGGGGGCGCTCACGCGGAGGGCGCCCCTCCCCGAGCCCTGGCGC TGATTATGTTCAATATTCCCAGGGGGGCGCTCGCGCGGAGGGCGCCCCTCCCCGAGCCCTGGCGC T C AC003688.2,CTDNEP1 Ensembl:ENSG00000262302,Ensembl:ENSG00000175826 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7252279..7252429 26863410 MeRIP-seq:(Medium) rs1251967176 Functional Loss SNV dbSNP153 33..33 33 - - - 104312 RMVar_ID_104312 Human_SNP_ID_616355196 m1A Human chr17 - 7254675 7254675 7254675 TGGTGACAGGAACAGGATCTGTCCTCTTGCACATGGCTCTCAAGGCTCCCAGCGGCCCCCCAGGA TGGTGACAGGAACAGGATCTGTCCTCTTGCACGTGGCTCTCAAGGCTCCCAGCGGCCCCCCAGGA T C AC003688.2 Ensembl:ENSG00000262302 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7254626..7254675 32194978 MeRIP-seq:(Medium) rs762426716 Functional Loss SNV dbSNP153 33..33 33 - - - 104313 RMVar_ID_104313 Human_SNP_ID_616356858 m1A Human chr17 - 7259805 7259805 7259805 TGCTTCCTGGCTCACAAGGCGGGGCTCCATAGACAAGGGGAACCAAGGTGGGGCAGGGACAGGGT TGCTTCCTGGCTCACAAGGCGGGGCTCCATAGGCAAGGGGAACCAAGGTGGGGCAGGGACAGGGT T C AC003688.2 Ensembl:ENSG00000262302 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7259767..7259840 26863196 MeRIP-seq:(Medium) rs543910780 Functional Loss SNV dbSNP153 33..33 33 - - - 104314 RMVar_ID_104314 Human_SNP_ID_616357334 m1A Human chr17 + 7260995 7260989 7260995 GGCTCGAGTGGCCTGCAAGGCCGCTGCGGGCGAGGGGAAAGGGCGCCGTCATTGCTGGAAATGCA GGCTCGAGTGGCCTGCAAGGCCGCTGC______GGGGAAAGGGCGCCGTCATTGCTGGAAATGCA CGGGCGA C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7260992..7261190 26863196 MeRIP-seq:(Medium) rs777744847 Functional Loss DEL dbSNP153 28..33 33 - - - 104315 RMVar_ID_104315 Human_SNP_ID_616357342 m1A Human chr17 + 7260995 7260995 7260995 GGCTCGAGTGGCCTGCAAGGCCGCTGCGGGCGAGGGGAAAGGGCGCCGTCATTGCTGGAAATGCA GGCTCGAGTGGCCTGCAAGGCCGCTGCGGGCGCGGGGAAAGGGCGCCGTCATTGCTGGAAATGCA A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7260992..7261190 26863196 MeRIP-seq:(Medium) rs576767384 Functional Loss SNV dbSNP153 33..33 33 - - - 104316 RMVar_ID_104316 Human_SNP_ID_616357774 m1A Human chr17 - 7262301 7262301 7262301 AGCGCCCGGAGGGAACCGCCTGGCCTTCGGGGACCACCAATTTTGTCTGGAACCACCCTCCCGGC AGCGCCCGGAGGGAACCGCCTGGCCTTCGGGGTCCACCAATTTTGTCTGGAACCACCCTCCCGGC T A CLDN7 Ensembl:ENSG00000181885 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7262251..7262325 26863196 MeRIP-seq:(Medium) rs1232050496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1770840,Human_Splice_Rec_1770864,Human_Splice_Rec_1770868 104317 RMVar_ID_104317 Human_SNP_ID_616358059 m1A Human chr17 - 7263369 7263369 7263369 GCGTGACAGAGTGCACAGCAATTGGCAGTCCAAGCCCAGGCCCGGGAGGGAAAGAGAAACGGGCG GCGTGACAGAGTGCACAGCAATTGGCAGTCCAGGCCCAGGCCCGGGAGGGAAAGAGAAACGGGCG T C CLDN7 Ensembl:ENSG00000181885 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7263360..7263563 26863196 MeRIP-seq:(Medium) rs563337530 Functional Loss SNV dbSNP153 33..33 33 - - - 104318 RMVar_ID_104318 Human_SNP_ID_616358081 m1A Human chr17 - 7263434 7263434 7263434 GCAGGGTGAGGGACCATGGACGACCACCTTAGAGAGCCAGATTATAGGGAGGACGGAACAGTGAG GCAGGGTGAGGGACCATGGACGACCACCTTAGGGAGCCAGATTATAGGGAGGACGGAACAGTGAG T C CLDN7 Ensembl:ENSG00000181885 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7263432..7263546 26863196 MeRIP-seq:(Medium) rs1011225245 Functional Loss SNV dbSNP153 33..33 33 - - - 104319 RMVar_ID_104319 Human_SNP_ID_616370976 m1A Human chr17 + 7307032 7307032 7307032 CCACACTAGCGCGCTAGAAGAGTGGGGCGGAAAGACATCTCCCGCGCATGTGTGGAACTGGGGGG CCACACTAGCGCGCTAGAAGAGTGGGGCGGAAGGACATCTCCCGCGCATGTGTGGAACTGGGGGG A G EIF5A Ensembl:ENSG00000132507 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7307027..7307115 26863196 MeRIP-seq:(Medium) rs772289588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18707984 Human_Splice_Rec_1771029 104320 RMVar_ID_104320 Human_SNP_ID_616371254 m1A Human chr17 + 7307646 7307643 7307646 GAGTCGGCGCCTGCGTACTAAGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGC GAGTCGGCGCCTGCGTACTAAGACCCGTGT___GCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGC TGCA T EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr17:7307501..7308152;chr17:7307545..7307830 26863196 MeRIP-seq:(Medium) rs981904428 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_50617,Human_RBP_ID_4464301,Human_RBP_ID_5318227,Human_RBP_ID_5497706,Human_RBP_ID_5526160,Human_RBP_ID_6641896,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154948,Human_RBP_ID_22442772,Human_RBP_ID_26970433 104321 RMVar_ID_104321 Human_SNP_ID_616371259 m1A Human chr17 + 7307666 7307646 7307667 AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGACCCGTGTGCA_____________________GCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGCAGCGGCGGCGGCGGTAGAG A EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7307626..7307700 32194978 MeRIP-seq:(Medium) rs751169482 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_50617,Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772,Human_RBP_ID_23129651,Human_RBP_ID_26645975 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104322 RMVar_ID_104322 Human_SNP_ID_616371260 m1A Human chr17 + 7307646 7307646 7307646 GAGTCGGCGCCTGCGTACTAAGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGC GAGTCGGCGCCTGCGTACTAAGACCCGTGTGCGGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGC A G EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr17:7307501..7308152;chr17:7307545..7307830 26863196 MeRIP-seq:(Medium) rs978638011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50617,Human_RBP_ID_4464301,Human_RBP_ID_5318227,Human_RBP_ID_5497706,Human_RBP_ID_5526160,Human_RBP_ID_6641896,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154948,Human_RBP_ID_22442772,Human_RBP_ID_26970433 104323 RMVar_ID_104323 Human_SNP_ID_616371263 m1A Human chr17 + 7307666 7307648 7307666 AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGACCCGTGTGCAGC__________________GGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG CAGCGGCGGCGGCGGTAGA C EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7307626..7307700 32194978 MeRIP-seq:(Medium) rs892585891 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_50617,Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772,Human_RBP_ID_23129651,Human_RBP_ID_26645975 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104324 RMVar_ID_104324 Human_SNP_ID_616371269 m1A Human chr17 + 7307666 7307649 7307667 AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGACCCGTGTGCAGCA__________________GCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGCGGCGGCGGCGGTAGAG A EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7307626..7307700 32194978 MeRIP-seq:(Medium) rs1236828729 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_50617,Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772,Human_RBP_ID_23129651,Human_RBP_ID_26645975 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104325 RMVar_ID_104325 Human_SNP_ID_616371272 m1A Human chr17 + 7307666 7307651 7307666 AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGACCCGTGTGCAGCAGC_______________GGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG CGGCGGCGGCGGTAGA C EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7307626..7307700 32194978 MeRIP-seq:(Medium) rs970696993 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_50617,Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772,Human_RBP_ID_23129651,Human_RBP_ID_26645975 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104326 RMVar_ID_104326 Human_SNP_ID_616371278 m1A Human chr17 + 7307666 7307666 7307666 AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG AGACCCGTGTGCAGCAGCGGCGGCGGCGGTAGCGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGG A C EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7307626..7307700 32194978 MeRIP-seq:(Medium) rs902712373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50617,Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772,Human_RBP_ID_23129651,Human_RBP_ID_26645975 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104327 RMVar_ID_104327 Human_SNP_ID_616371295 m1A Human chr17 + 7307685 7307685 7307685 GCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGGCAGCGGTTGGGCTCGCGGC GCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCGGCGGGCTCGGAGGCAGCGGTTGGGCTCGCGGC A G EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7307493..7308145;chr17:7307551..7308075;chr17:7307551..7307851;chr17:7307501..7308150;chr17:7307501..7308408 26863196 MeRIP-seq:(Medium) rs906626756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_6641900,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 104328 RMVar_ID_104328 Human_SNP_ID_616371418 m1A Human chr17 + 7308036 7308036 7308036 GGGAGAGGCCGCCAGGCGGCCACGCCGGGGCGAGGGCCAGGGGCCAGATCGGCCCACCGGGGCAA GGGAGAGGCCGCCAGGCGGCCACGCCGGGGCGGGGGCCAGGGGCCAGATCGGCCCACCGGGGCAA A G EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7308026..7308075 26863196 MeRIP-seq:(Medium) rs1273107548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542577,Human_RBP_ID_4464303,Human_RBP_ID_5366223,Human_RBP_ID_21974146 Human_Splice_Rec_1771083,Human_Splice_Rec_1771093,Human_Splice_Rec_1771105 104329 RMVar_ID_104329 Human_SNP_ID_616372025 m1A Human chr17 + 7309556 7309556 7309556 GTTGGGAAAATGTTTCTGGAGAGAAATGGGATAGATTGGAGGTCCTGTTGACCTCCATGCTTATT GTTGGGAAAATGTTTCTGGAGAGAAATGGGATGGATTGGAGGTCCTGTTGACCTCCATGCTTATT A G EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr17:7309549..7309775;chr17:7309554..7309825 26863410,26863196 MeRIP-seq:(Medium) rs1340603205 Functional Loss SNV dbSNP153 33..33 33 - - - 104330 RMVar_ID_104330 Human_SNP_ID_616372030 m1A Human chr17 - 7309569 7309569 7309569 GAGAACTGAAGTGAATAAGCATGGAGGTCAACAGGACCTCCAATCTATCCCATTTCTCTCCAGAA GAGAACTGAAGTGAATAAGCATGGAGGTCAACTGGACCTCCAATCTATCCCATTTCTCTCCAGAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7309567..7309801 26863196 MeRIP-seq:(Medium) rs1439155775 Functional Loss SNV dbSNP153 33..33 33 - - - 104331 RMVar_ID_104331 Human_SNP_ID_616372031 m1A Human chr17 - 7309569 7309569 7309569 GAGAACTGAAGTGAATAAGCATGGAGGTCAACAGGACCTCCAATCTATCCCATTTCTCTCCAGAA GAGAACTGAAGTGAATAAGCATGGAGGTCAACCGGACCTCCAATCTATCCCATTTCTCTCCAGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7309567..7309801 26863196 MeRIP-seq:(Medium) rs1439155775 Functional Loss SNV dbSNP153 33..33 33 - - - 104332 RMVar_ID_104332 Human_SNP_ID_616372053 m1A Human chr17 + 7309665 7309665 7309665 AAAATGGCAGATGACTTGGACTTCGAGACAGGAGATGCAGGGGCCTCAGCCACCTTCCCAATGCA AAAATGGCAGATGACTTGGACTTCGAGACAGGGGATGCAGGGGCCTCAGCCACCTTCCCAATGCA A G EIF5A Ensembl:ENSG00000132507 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7309517..7309700 26863196 MeRIP-seq:(Medium) rs779781729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499022,Human_RBP_ID_1184091,Human_RBP_ID_1541458,Human_RBP_ID_1868702,Human_RBP_ID_3536729,Human_RBP_ID_4466048,Human_RBP_ID_6641905,Human_RBP_ID_8253664,Human_RBP_ID_8462421,Human_RBP_ID_8822046,Human_RBP_ID_8941804,Human_RBP_ID_9076106,Human_RBP_ID_13154972,Human_RBP_ID_17261819,Human_RBP_ID_17493860,Human_RBP_ID_18707986 Human_Splice_Rec_1771030,Human_Splice_Rec_1771040,Human_Splice_Rec_1771044,Human_Splice_Rec_1771054,Human_Splice_Rec_1771062,Human_Splice_Rec_1771072,Human_Splice_Rec_1771082,Human_Splice_Rec_1771084,Human_Splice_Rec_1771096,Human_Splice_Rec_1771106,Human_Splice_Rec_1771114 RMVar_hsa_circ_109726,RMVar_hsa_circ_181788,RMVar_hsa_circ_106755,RMVar_hsa_circ_181787 104333 RMVar_ID_104333 Human_SNP_ID_616372140 m1A Human chr17 - 7309918 7309914 7309918 GAATGGGTATGAAGGCTGAGCGCTAAACAAAAACAATCAGACAGTAAAAGCAGAGTTAAAGGAAA GAATGGGTATGAAGGCTGAGCGCTAAACAAAA____TCAGACAGTAAAAGCAGAGTTAAAGGAAA ATTGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7309915..7310079 26863196 MeRIP-seq:(Medium) rs767355832 Functional Loss DEL dbSNP153 33..36 33 - - - 104334 RMVar_ID_104334 Human_SNP_ID_616372563 m1A Human chr17 + 7311004 7311004 7311004 CGTTTTAGAGTTTGGTTGGGTTTCTCTTTGTGATGCATACATACAGGTCCATCTGGTTGGTATTG CGTTTTAGAGTTTGGTTGGGTTTCTCTTTGTGTTGCATACATACAGGTCCATCTGGTTGGTATTG A T EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7311001..7311050 26863196 MeRIP-seq:(Medium) rs746996013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1541467,Human_RBP_ID_8462426 RMVar_hsa_circ_109726,RMVar_hsa_circ_181788,RMVar_hsa_circ_106755,RMVar_hsa_circ_181787 104335 RMVar_ID_104335 Human_SNP_ID_616372874 m1A Human chr17 - 7311911 7311911 7311911 AAAATAAAACGTCAAATAAATTGTGTAGGAGGAGTCCAGCTTAGGACCGGGCCAGAGCCAGGCCA AAAATAAAACGTCAAATAAATTGTGTAGGAGGCGTCCAGCTTAGGACCGGGCCAGAGCCAGGCCA T G GPS2 Ensembl:ENSG00000132522 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7311862..7312165 26863196 MeRIP-seq:(Medium) rs187784355 Functional Loss SNV dbSNP153 33..33 33 - - - 104336 RMVar_ID_104336 Human_SNP_ID_616372893 m1A Human chr17 - 7311947 7311947 7311947 GGGGCTCCCCGACAGATTGAGGGGGTGGGGAAAACCAAAATAAAACGTCAAATAAATTGTGTAGG GGGGCTCCCCGACAGATTGAGGGGGTGGGGAATACCAAAATAAAACGTCAAATAAATTGTGTAGG T A GPS2 Ensembl:ENSG00000132522 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:7311863..7311947 26863410 MeRIP-seq:(Medium) rs1453034246 Functional Loss SNV dbSNP153 33..33 33 - - - 104337 RMVar_ID_104337 Human_SNP_ID_616372899 m1A Human chr17 - 7311964 7311964 7311964 GAGCTAGGTGAAGGGCAGGGGCTCCCCGACAGATTGAGGGGGTGGGGAAAACCAAAATAAAACGT GAGCTAGGTGAAGGGCAGGGGCTCCCCGACAGGTTGAGGGGGTGGGGAAAACCAAAATAAAACGT T C GPS2 Ensembl:ENSG00000132522 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7311869..7312236 26863410 MeRIP-seq:(Medium) rs1201823480 Functional Loss SNV dbSNP153 33..33 33 - - - 104338 RMVar_ID_104338 Human_SNP_ID_616372911 m1A Human chr17 - 7311999 7311999 7311999 ACCAAGGCCACAGCTTCGCTCGCTCCTGGCCAAGGGAGCTAGGTGAAGGGCAGGGGCTCCCCGAC ACCAAGGCCACAGCTTCGCTCGCTCCTGGCCAGGGGAGCTAGGTGAAGGGCAGGGGCTCCCCGAC T C GPS2 Ensembl:ENSG00000132522 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7311779..7312380 26863196 MeRIP-seq:(Medium) rs1482731069 Functional Loss SNV dbSNP153 33..33 33 - - - 104339 RMVar_ID_104339 Human_SNP_ID_616373026 m1A Human chr17 - 7312226 7312226 7312226 GTCCCCAGTCTGTTGGGGTGGTGCTCAGGGTAAAGGGCTATAGGCAACAGGGGACCAGACCAGGG GTCCCCAGTCTGTTGGGGTGGTGCTCAGGGTACAGGGCTATAGGCAACAGGGGACCAGACCAGGG T G GPS2 Ensembl:ENSG00000132522 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7312176..7312225 26863196 MeRIP-seq:(Medium) rs986508097 Functional Loss SNV dbSNP153 33..33 33 - - - 104340 RMVar_ID_104340 Human_SNP_ID_616373747 m1A Human chr17 + 7313650 7313650 7313650 GGTGGGGGCTGAGCAGTCCCATAGGCACCACCAGGACTGCCTTGGAATTGTCCATGCTCTGGTGT GGTGGGGGCTGAGCAGTCCCATAGGCACCACCGGGACTGCCTTGGAATTGTCCATGCTCTGGTGT A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7313601..7313700 32194978 MeRIP-seq:(Medium) rs1376544413 Functional Loss SNV dbSNP153 33..33 33 - - - 104341 RMVar_ID_104341 Human_SNP_ID_616374125 m1A Human chr17 - 7314551 7314551 7314551 GATAAGATGATGGAACAGAAGATGAAGGAAGAACAGGAGAGAAGGAAGAAAAAGGAGATGGAAGA GATAAGATGATGGAACAGAAGATGAAGGAAGAGCAGGAGAGAAGGAAGAAAAAGGAGATGGAAGA T C GPS2,AC026954.2 Ensembl:ENSG00000132522,Ensembl:ENSG00000261915 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7314276..7315375 26863196 MeRIP-seq:(Medium) rs1465011355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236214,Human_RBP_ID_898230,Human_RBP_ID_1546629,Human_RBP_ID_2522226,Human_RBP_ID_4449200,Human_RBP_ID_5648794,Human_RBP_ID_18987825,Human_RBP_ID_22959346,Human_RBP_ID_24544974,Human_RBP_ID_27812226 Human_Splice_Rec_1771124,Human_Splice_Rec_1771125,Human_Splice_Rec_1771146,Human_Splice_Rec_1771147,Human_Splice_Rec_1771163,Human_Splice_Rec_1771188,Human_Splice_Rec_1771189,Human_Splice_Rec_1771210,Human_Splice_Rec_1771211,Human_Splice_Rec_1771229,Human_Splice_Rec_1771244,Human_Splice_Rec_1771245,Human_Splice_Rec_1771260,Human_Splice_Rec_1771261,Human_Splice_Rec_1771270,Human_Splice_Rec_1771271,Human_Splice_Rec_1771280,Human_Splice_Rec_1771281,Human_Splice_Rec_1771287,Human_Splice_Rec_1771293,Human_Splice_Rec_1771300,Human_Splice_Rec_1771301,Human_Splice_Rec_1771322,Human_Splice_Rec_1771323,Human_Splice_Rec_1771358,Human_Splice_Rec_1771359 RMVar_hsa_circ_6806,RMVar_hsa_circ_105419,RMVar_hsa_circ_125684,RMVar_hsa_circ_98644,RMVar_hsa_circ_181793,RMVar_hsa_circ_101835,RMVar_hsa_circ_181794,RMVar_hsa_circ_181792,RMVar_hsa_circ_345191,RMVar_hsa_circ_87846,RMVar_hsa_circ_307225,RMVar_hsa_circ_181795,RMVar_hsa_circ_181799,RMVar_hsa_circ_83586,RMVar_hsa_circ_368654,RMVar_hsa_circ_181802,RMVar_hsa_circ_359313 104342 RMVar_ID_104342 Human_SNP_ID_616374337 m1A Human chr17 - 7315070 7315056 7315071 GCAGTCAGAGACAGCCGGGCGCCCACGGCCCGAGCGCCCACGGCAGCACCATGCCCGCACTCCTG GCAGTCAGAGACAGCCGGGCGCCCACGGCCC_______________CACCATGCCCGCACTCCTG GCTGCCGTGGGCGCTC G GPS2,AC026954.2 Ensembl:ENSG00000132522,Ensembl:ENSG00000261915 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7315032..7315319 26863196 MeRIP-seq:(Medium) rs1269657956 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_4465132,Human_RBP_ID_9375277,Human_RBP_ID_23257118,Human_RBP_ID_26332823 Human_Splice_Rec_1771162,Human_Splice_Rec_1771208,Human_Splice_Rec_1771228,Human_Splice_Rec_1771242,Human_Splice_Rec_1771258,Human_Splice_Rec_1771268,Human_Splice_Rec_1771278,Human_Splice_Rec_1771298,Human_Splice_Rec_1771320,Human_Splice_Rec_1771356 RMVar_hsa_circ_6806,RMVar_hsa_circ_105419,RMVar_hsa_circ_98644,RMVar_hsa_circ_181793,RMVar_hsa_circ_101835,RMVar_hsa_circ_181794,RMVar_hsa_circ_87846,RMVar_hsa_circ_181795,RMVar_hsa_circ_181799,RMVar_hsa_circ_83586,RMVar_hsa_circ_181802 104343 RMVar_ID_104343 Human_SNP_ID_616374360 m1A Human chr17 - 7315100 7315100 7315100 CGCCTCCCCGCAGGCCCCGTCTGAGGTCTGGCAGTCAGAGACAGCCGGGCGCCCACGGCCCGAGC CGCCTCCCCGCAGGCCCCGTCTGAGGTCTGGCCGTCAGAGACAGCCGGGCGCCCACGGCCCGAGC T G GPS2,AC026954.2 Ensembl:ENSG00000132522,Ensembl:ENSG00000261915 Protein coding,Protein coding CDS,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7315001..7315290 26863410 MeRIP-seq:(Medium) rs200170373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499060,Human_RBP_ID_4465132,Human_RBP_ID_9375277,Human_RBP_ID_19078245 Human_Splice_Rec_1771162,Human_Splice_Rec_1771208,Human_Splice_Rec_1771228,Human_Splice_Rec_1771242,Human_Splice_Rec_1771258,Human_Splice_Rec_1771268,Human_Splice_Rec_1771278,Human_Splice_Rec_1771298,Human_Splice_Rec_1771320,Human_Splice_Rec_1771356 RMVar_hsa_circ_6806,RMVar_hsa_circ_105419,RMVar_hsa_circ_98644,RMVar_hsa_circ_181793,RMVar_hsa_circ_101835,RMVar_hsa_circ_181794,RMVar_hsa_circ_87846,RMVar_hsa_circ_181795,RMVar_hsa_circ_181799,RMVar_hsa_circ_83586,RMVar_hsa_circ_181802 104344 RMVar_ID_104344 Human_SNP_ID_616376612 m1A Human chr17 + 7321436 7321436 7321436 ACCAGGATGTGCATCGTGTCATCTGCCCCCCGACGAACACCCACACGGCTCCCCACCTAGGACCG ACCAGGATGTGCATCGTGTCATCTGCCCCCCGGCGAACACCCACACGGCTCCCCACCTAGGACCG A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7321210..7321931 26863196 MeRIP-seq:(Medium) rs765271566 Functional Loss SNV dbSNP153 33..33 33 - - - 104345 RMVar_ID_104345 Human_SNP_ID_616378750 m1A Human chr17 + 7327726 7327726 7327726 CGGTCCCCTTCACCAAGCTGGTCCAGGTCCTGACCATACTCCTCCAACACAGAGCGTCCATCTCT CGGTCCCCTTCACCAAGCTGGTCCAGGTCCTGGCCATACTCCTCCAACACAGAGCGTCCATCTCT A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7327677..7327760 26863196 MeRIP-seq:(Medium) rs1414017722 Functional Loss SNV dbSNP153 33..33 33 - - - 104346 RMVar_ID_104346 Human_SNP_ID_616379176 m1A Human chr17 - 7329209 7329209 7329209 CCCCAGCGGGAGCGGCTCAGGACCGGGGTCCAACGGGGGTCTGGGCAGCGGCGGGGAACTGCACC CCCCAGCGGGAGCGGCTCAGGACCGGGGTCCAGCGGGGGTCTGGGCAGCGGCGGGGAACTGCACC T C NEURL4 Ensembl:ENSG00000215041 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7329196..7329327 26863196 MeRIP-seq:(Medium) rs534774549 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6690,Human_RBP_ID_237184,Human_RBP_ID_822748,Human_RBP_ID_897313,Human_RBP_ID_3950065,Human_RBP_ID_5143089,Human_RBP_ID_5363675,Human_RBP_ID_8189317,Human_RBP_ID_8232285,Human_RBP_ID_9326453,Human_RBP_ID_9422212,Human_RBP_ID_18419862,Human_RBP_ID_18941319,Human_RBP_ID_19084935,Human_RBP_ID_21974150,Human_RBP_ID_22715938,Human_RBP_ID_23210222,Human_RBP_ID_26331186,Human_RBP_ID_26769265,Human_RBP_ID_27812229 RMVar_hsa_circ_115420,RMVar_hsa_circ_181811 104347 RMVar_ID_104347 Human_SNP_ID_616385127 m1A Human chr17 + 7350429 7350429 7350429 TGCGCGAAGTGTGCACTGGGACGTGGAGTAGAAGGCAGGCGGGAGGGCGGGCAGGGTGCAAGGAT TGCGCGAAGTGTGCACTGGGACGTGGAGTAGACGGCAGGCGGGAGGGCGGGCAGGGTGCAAGGAT A C ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7350427..7350534 26863196 MeRIP-seq:(Medium) rs953203276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124872,RMVar_hsa_circ_181825,RMVar_hsa_circ_87945,RMVar_hsa_circ_119438,RMVar_hsa_circ_121471,RMVar_hsa_circ_181826,RMVar_hsa_circ_181827,RMVar_hsa_circ_89459,RMVar_hsa_circ_181828,RMVar_hsa_circ_181829 104348 RMVar_ID_104348 Human_SNP_ID_616385425 m1A Human chr17 - 7351420 7351420 7351421 TGGCAGAGGGCCCGGTGGCGGGGAAGGGAGGCAGGCGCGGGCCCCGTGGGCCTCGGGTCACAGCG TGGCAGAGGGCCCGGTGGCGGGGAAGGGAGGTGGGCGCGGGCCCCGTGGGCCTCGGGTCACAGCG TG CA lnc-NEURL4-3,lnc-NEURL4-3:2 RNACentral:URS0000D5761C,RNACentral:URS0000D584FE lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7351200..7351511 26863196 MeRIP-seq:(Medium) rs386795019 Functional Loss MNV dbSNP153 32..33 33 - - - 104349 RMVar_ID_104349 Human_SNP_ID_616385426 m1A Human chr17 - 7351420 7351420 7351420 TGGCAGAGGGCCCGGTGGCGGGGAAGGGAGGCAGGCGCGGGCCCCGTGGGCCTCGGGTCACAGCG TGGCAGAGGGCCCGGTGGCGGGGAAGGGAGGCCGGCGCGGGCCCCGTGGGCCTCGGGTCACAGCG T G lnc-NEURL4-3,lnc-NEURL4-3:2 RNACentral:URS0000D5761C,RNACentral:URS0000D584FE lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7351200..7351511 26863196 MeRIP-seq:(Medium) rs1454659506 Functional Loss SNV dbSNP153 33..33 33 - - - 104350 RMVar_ID_104350 Human_SNP_ID_616386460 m1A Human chr17 + 7354761 7354761 7354761 ATAGCTGGGGAAGGCCCAAGGCCGCCCAGGGCAGAGAGAGGAGACGAAGAGTTTGGGACAGTGGG ATAGCTGGGGAAGGCCCAAGGCCGCCCAGGGCGGAGAGAGGAGACGAAGAGTTTGGGACAGTGGG A G KCTD11 Ensembl:ENSG00000213859 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7352826..7354860 26863196 MeRIP-seq:(Medium) rs1229768908 Functional Loss SNV dbSNP153 33..33 33 - - - 104351 RMVar_ID_104351 Human_SNP_ID_616395180 m1A Human chr17 - 7384587 7384587 7384587 CTGCAGGATGAGGTACGGTGGGACCCCGGCCCAGGGTTCCTCGCCCCCGGAGAACATCTCCCACA CTGCAGGATGAGGTACGGTGGGACCCCGGCCCGGGGTTCCTCGCCCCCGGAGAACATCTCCCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7384560..7384778 26863196 MeRIP-seq:(Medium) rs1213412714 Functional Loss SNV dbSNP153 33..33 33 - - - 104352 RMVar_ID_104352 Human_SNP_ID_616397787 m1A Human chr17 + 7393237 7393237 7393237 ACCTCACGGTCCCCGGGGTCGGCCAGGCGGACACGCAGCGGCCGGCGGGCGCCACAGCACAGACG ACCTCACGGTCCCCGGGGTCGGCCAGGCGGACTCGCAGCGGCCGGCGGGCGCCACAGCACAGACG A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7393143..7393296 26863196 MeRIP-seq:(Medium) rs779564941 Functional Loss SNV dbSNP153 33..33 33 - - - 104353 RMVar_ID_104353 Human_SNP_ID_616401288 m1A Human chr17 + 7405035 7405035 7405035 AGCCTCCCCTCACCCCCGCCTTCCCTCCTAGGATCCGCGCTGACCCCCGCCCCGGGGCTCTGGAC AGCCTCCCCTCACCCCCGCCTTCCCTCCTAGGGTCCGCGCTGACCCCCGCCCCGGGGCTCTGGAC A G NLGN2 Ensembl:ENSG00000169992 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr17:7404935..7405081;chr17:7404945..7405035 26863410 MeRIP-seq:(Medium) rs556046189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238087,Human_RBP_ID_4449875,Human_RBP_ID_5420466,Human_RBP_ID_9326456,Human_RBP_ID_19078266,Human_RBP_ID_22542888,Human_RBP_ID_22657354,Human_RBP_ID_25335277,Human_RBP_ID_26970672,Human_RBP_ID_27456686 104354 RMVar_ID_104354 Human_SNP_ID_616402106 m1A Human chr17 - 7407955 7407955 7407955 CAGGGAGGCAGGATACAGACAGACGGACAGACAGAAAAATACAGAGGTGGAAGAGGGCAAGGGAA CAGGGAGGCAGGATACAGACAGACGGACAGACGGAAAAATACAGAGGTGGAAGAGGGCAAGGGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7407921..7408052 26863196 MeRIP-seq:(Medium) rs150220358 Functional Loss SNV dbSNP153 33..33 33 - - - 104355 RMVar_ID_104355 Human_SNP_ID_616402107 m1A Human chr17 - 7407955 7407955 7407955 CAGGGAGGCAGGATACAGACAGACGGACAGACAGAAAAATACAGAGGTGGAAGAGGGCAAGGGAA CAGGGAGGCAGGATACAGACAGACGGACAGACCGAAAAATACAGAGGTGGAAGAGGGCAAGGGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7407921..7408052 26863196 MeRIP-seq:(Medium) rs150220358 Functional Loss SNV dbSNP153 33..33 33 - - - 104356 RMVar_ID_104356 Human_SNP_ID_616404692 m1A Human chr17 + 7416973 7416973 7416973 GGTGCCGCAGGATACCAAGTTCATCCACACCAAGCCCAATCGCTTCGAGGAGGTGGTGTGGAGCA GGTGCCGCAGGATACCAAGTTCATCCACACCAGGCCCAATCGCTTCGAGGAGGTGGTGTGGAGCA A G NLGN2 Ensembl:ENSG00000169992 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7415792..7417660 32194978 MeRIP-seq:(Medium) rs140406892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499482,Human_RBP_ID_1288835,Human_RBP_ID_1369777 Human_Splice_Rec_1772172,Human_Splice_Rec_1772186 104357 RMVar_ID_104357 Human_SNP_ID_616405501 m1A Human chr17 - 7419101 7419101 7419101 GAGGGTGGTCAGCTGAGGAGAAGGCTGGTCTGACACTGAGATGGGGACAGCTTCAAAGAGGGGGA GAGGGTGGTCAGCTGAGGAGAAGGCTGGTCTGGCACTGAGATGGGGACAGCTTCAAAGAGGGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7419066..7419248 26863196 MeRIP-seq:(Medium) rs1238741310 Functional Loss SNV dbSNP153 33..33 33 - - - 104358 RMVar_ID_104358 Human_SNP_ID_616416369 m1A Human chr17 - 7455638 7455638 7455638 CCCTCCAGCAGTGATCTCTCTAGCCTTGTGCAACTTCTTCCACCGCCTCTGTTTTAGTTCCCACC CCCTCCAGCAGTGATCTCTCTAGCCTTGTGCAGCTTCTTCCACCGCCTCTGTTTTAGTTCCCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7455629..7455778 26863196 MeRIP-seq:(Medium) rs887277736 Functional Loss SNV dbSNP153 33..33 33 - - - 104359 RMVar_ID_104359 Human_SNP_ID_616416370 m1A Human chr17 + 7455650 7455650 7455650 AACAGAGGCGGTGGAAGAAGTTGCACAAGGCTAGAGAGATCACTGCTGGAGGGAAAAGCATGATG AACAGAGGCGGTGGAAGAAGTTGCACAAGGCTGGAGAGATCACTGCTGGAGGGAAAAGCATGATG A G CHRNB1 Ensembl:ENSG00000170175 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7455621..7455785 26863196 MeRIP-seq:(Medium) rs527273543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181843,RMVar_hsa_circ_102020 104360 RMVar_ID_104360 Human_SNP_ID_616417777 m1A Human chr17 + 7461007 7461007 7461007 TTCTGGCTATTTGGTCTAGTCTGGGAGAAACCATCAGGAAAAAAAAACAGGGAGAAAGTAGATTC TTCTGGCTATTTGGTCTAGTCTGGGAGAAACCGTCAGGAAAAAAAAACAGGGAGAAAGTAGATTC A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7460958..7461059 32194978 MeRIP-seq:(Medium) rs1283513143 Functional Loss SNV dbSNP153 33..33 33 - - - 104361 RMVar_ID_104361 Human_SNP_ID_616417930 m1A Human chr17 - 7461657 7461657 7461657 TTCCATCCCTTCTCCAGCCCTTGGGGCAACTGAGCAATATACTTAACCTGAATCTCTACTCACAG TTCCATCCCTTCTCCAGCCCTTGGGGCAACTGGGCAATATACTTAACCTGAATCTCTACTCACAG T C ZBTB4 Ensembl:ENSG00000174282 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7461606..7461706 32194978 MeRIP-seq:(Medium) rs1465416749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526170,Human_RBP_ID_6643788 Human_miRNA_ID_268571,Human_miRNA_ID_2049849,Human_miRNA_ID_2765927 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104362 RMVar_ID_104362 Human_SNP_ID_616418181 m1A Human chr17 - 7462454 7462454 7462454 TGGCGGGAGCACTGCTGCTGAGGAAGCTTCCGAGACCGCCTCACTCCAGGACCCTATCATTTCAG TGGCGGGAGCACTGCTGCTGAGGAAGCTTCCGCGACCGCCTCACTCCAGGACCCTATCATTTCAG T G ZBTB4 Ensembl:ENSG00000174282 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7462403..7462653 32194978 MeRIP-seq:(Medium) rs1399646583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899315,Human_RBP_ID_8463086,Human_RBP_ID_22061938 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104363 RMVar_ID_104363 Human_SNP_ID_616418225 m1A Human chr17 - 7462577 7462577 7462577 GCCCGGGGGCACCCCAACCCCTGTCATTGCCTATTCCAAGGGCAGCGCTGGCACCAGGCCCGGGG GCCCGGGGGCACCCCAACCCCTGTCATTGCCTCTTCCAAGGGCAGCGCTGGCACCAGGCCCGGGG T G ZBTB4 Ensembl:ENSG00000174282 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7462527..7462654 26863196 MeRIP-seq:(Medium) rs1278382542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22063007 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104364 RMVar_ID_104364 Human_SNP_ID_616418329 m1A Human chr17 - 7462801 7462801 7462801 GCGGGACGTGCCCGCACAGAGCGGAGGCACCGATGCGGGGACTGTGCCCAGACCTTCACCACCCT GCGGGACGTGCCCGCACAGAGCGGAGGCACCGGTGCGGGGACTGTGCCCAGACCTTCACCACCCT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7462751..7463001 32194978 MeRIP-seq:(Medium) rs756087662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9257614,Human_RBP_ID_27456955 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104365 RMVar_ID_104365 Human_SNP_ID_616418480 m1A Human chr17 - 7463072 7463072 7463072 GGAGCTGAGCGGAGAGGAGATGGAGGAGAGTGAGGAGGACGAAGAGGAGGAGGACGAAGAGGAGG GGAGCTGAGCGGAGAGGAGATGGAGGAGAGTGTGGAGGACGAAGAGGAGGAGGACGAAGAGGAGG T A ZBTB4 Ensembl:ENSG00000174282 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7462779..7463237 26863196 MeRIP-seq:(Medium) rs767628650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2522718,Human_RBP_ID_6643831,Human_RBP_ID_25324905 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104366 RMVar_ID_104366 Human_SNP_ID_616418768 m1A Human chr17 + 7463671 7463671 7463671 GGGGCCGGTGTGTTGAGGGTTGGAGAAAGGGGAGCCTCCGGGGCTCCCTGGCTGTAGGTCTTGTA GGGGCCGGTGTGTTGAGGGTTGGAGAAAGGGGGGCCTCCGGGGCTCCCTGGCTGTAGGTCTTGTA A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7463623..7463798 26863196 MeRIP-seq:(Medium) rs746224440 Functional Loss SNV dbSNP153 33..33 33 - - - 104367 RMVar_ID_104367 Human_SNP_ID_616419801 m1A Human chr17 + 7466420 7466420 7466420 ATCAGAAAACGCAGCTGCTGGGACTCCTGGCAACTCCAGGACCCGGGGTGGGGAAGAAGCAGGGG ATCAGAAAACGCAGCTGCTGGGACTCCTGGCAGCTCCAGGACCCGGGGTGGGGAAGAAGCAGGGG A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7466165..7466564 32194978 MeRIP-seq:(Medium) rs760863659 Functional Loss SNV dbSNP153 33..33 33 - - - 104368 RMVar_ID_104368 Human_SNP_ID_616419862 m1A Human chr17 + 7466523 7466523 7466523 GAAGAAGAAGCAGAGGAGGAAGAAGAGGAAGAAGACGAGGAAGAGGAGGAGGAGGAAGAGGCAGC GAAGAAGAAGCAGAGGAGGAAGAAGAGGAAGACGACGAGGAAGAGGAGGAGGAGGAAGAGGCAGC A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7466473..7466775 26863196 MeRIP-seq:(Medium) rs150471906 Functional Loss SNV dbSNP153 33..33 33 - - - 104369 RMVar_ID_104369 Human_SNP_ID_616419863 m1A Human chr17 + 7466523 7466523 7466523 GAAGAAGAAGCAGAGGAGGAAGAAGAGGAAGAAGACGAGGAAGAGGAGGAGGAGGAAGAGGCAGC GAAGAAGAAGCAGAGGAGGAAGAAGAGGAAGAGGACGAGGAAGAGGAGGAGGAGGAAGAGGCAGC A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7466473..7466775 26863196 MeRIP-seq:(Medium) rs150471906 Functional Loss SNV dbSNP153 33..33 33 - - - 104370 RMVar_ID_104370 Human_SNP_ID_616419978 m1A Human chr17 + 7466800 7466800 7466800 GGGACGGGTCCGTCACCTCTGCAGGGGGGGGCATGGTGCCAGCCTAGACAGTGGGAGAAGAGGCC GGGACGGGTCCGTCACCTCTGCAGGGGGGGGCTTGGTGCCAGCCTAGACAGTGGGAGAAGAGGCC A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7466440..7466830 26863196 MeRIP-seq:(Medium) rs1352985979 Functional Loss SNV dbSNP153 33..33 33 - - - 104371 RMVar_ID_104371 Human_SNP_ID_616423199 m1A Human chr17 - 7479300 7479300 7479300 GGTTGACCTGGGGGCGCAGGGGTCGGGGGCTGAGCCTGGCCCCGCCCCCGGGCGCGCACGACGCT GGTTGACCTGGGGGCGCAGGGGTCGGGGGCTGGGCCTGGCCCCGCCCCCGGGCGCGCACGACGCT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7479293..7479560 26863196 MeRIP-seq:(Medium) rs1311705408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236813,Human_RBP_ID_3542595,Human_RBP_ID_5186065,Human_RBP_ID_8189325 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 104372 RMVar_ID_104372 Human_SNP_ID_616428653 m1A Human chr17 - 7495927 7495924 7495928 CCGTCACAGACATTCGCTTCTGCAAAGAAAGAAAGGCCAACAACTGAACAGCGTTCCTAGTTTCT CCGTCACAGACATTCGCTTCTGCAAAGAAAG____GCCAACAACTGAACAGCGTTCCTAGTTTCT CCTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7495926..7496000 26863196 MeRIP-seq:(Medium) rs3216887 Functional Loss DEL dbSNP153 32..35 33 - - - 104373 RMVar_ID_104373 Human_SNP_ID_616428696 m1A Human chr17 - 7496041 7496041 7496041 CTGCACATGTTTGGCAGCGGCCAGTCCGCTCAATCACCCCCTGCCTCGGGTCCATCAGCCCCCCA CTGCACATGTTTGGCAGCGGCCAGTCCGCTCAGTCACCCCCTGCCTCGGGTCCATCAGCCCCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7495991..7496084 26863196 MeRIP-seq:(Medium) rs368826061 Functional Loss SNV dbSNP153 33..33 33 - - - 104374 RMVar_ID_104374 Human_SNP_ID_616428700 m1A Human chr17 + 7496049 7496049 7496049 TGATGGACCCGAGGCAGGGGGTGATTGAGCGGACTGGCCGCTGCCAAACATGTGCAGGTAAGTGC TGATGGACCCGAGGCAGGGGGTGATTGAGCGGGCTGGCCGCTGCCAAACATGTGCAGGTAAGTGC A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7495914..7496075 26863196 MeRIP-seq:(Medium) rs1246243879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1288955,Human_RBP_ID_5467020,Human_RBP_ID_8822251,Human_RBP_ID_9257733,Human_RBP_ID_9288702,Human_RBP_ID_13166681,Human_RBP_ID_22959347,Human_RBP_ID_23749758,Human_RBP_ID_27813373 Human_Splice_Rec_1772391,Human_Splice_Rec_1772445 RMVar_hsa_circ_365876,RMVar_hsa_circ_377037,RMVar_hsa_circ_25082 104375 RMVar_ID_104375 Human_SNP_ID_616428874 m1A Human chr17 + 7496577 7496577 7496577 GGGGAGGAGATGGACAACAAGTTCGGTGTGGAACAACCTGAGGGTGACGAGGATCTGACCAAAGA GGGGAGGAGATGGACAACAAGTTCGGTGTGGAGCAACCTGAGGGTGACGAGGATCTGACCAAAGA A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7496526..7496647;chr17:7496526..7496625 26863196 MeRIP-seq:(Medium) rs767633932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6696,Human_RBP_ID_49407,Human_RBP_ID_1288956,Human_RBP_ID_1869284,Human_RBP_ID_3951777,Human_RBP_ID_4452041,Human_RBP_ID_5497819,Human_RBP_ID_5525309,Human_RBP_ID_5582985,Human_RBP_ID_6644672,Human_RBP_ID_8822260,Human_RBP_ID_9288704,Human_RBP_ID_13166689,Human_RBP_ID_22741088,Human_RBP_ID_23749765 Human_Splice_Rec_1772395,Human_Splice_Rec_1772449 RMVar_hsa_circ_85438,RMVar_hsa_circ_365876,RMVar_hsa_circ_377037,RMVar_hsa_circ_25082,RMVar_hsa_circ_101531,RMVar_hsa_circ_181845,RMVar_hsa_circ_181846 104376 RMVar_ID_104376 Human_SNP_ID_616428952 m1A Human chr17 + 7496797 7496797 7496797 GCCATGGTGGCTGTGGGCGGTACCAGCCCAGGATCCGGCGTTCTGGCCTAGAGCTGTATGCGGAA GCCATGGTGGCTGTGGGCGGTACCAGCCCAGGGTCCGGCGTTCTGGCCTAGAGCTGTATGCGGAA A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7496764..7496836 26863196 MeRIP-seq:(Medium) rs1341830523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_902068,Human_RBP_ID_1869286,Human_RBP_ID_3951778,Human_RBP_ID_5143459,Human_RBP_ID_8463368,Human_RBP_ID_8822265,Human_RBP_ID_9257734,Human_RBP_ID_9288705,Human_RBP_ID_9375280,Human_RBP_ID_18987846,Human_RBP_ID_19078273,Human_RBP_ID_22959348,Human_RBP_ID_23210223 Human_Splice_Rec_1772396,Human_Splice_Rec_1772450 Human_miRNA_ID_1983505,Human_miRNA_ID_2041032,Human_miRNA_ID_3020016 RMVar_hsa_circ_40743,RMVar_hsa_circ_85438,RMVar_hsa_circ_365876,RMVar_hsa_circ_377037,RMVar_hsa_circ_25082,RMVar_hsa_circ_101531,RMVar_hsa_circ_181845,RMVar_hsa_circ_120171,RMVar_hsa_circ_181846,RMVar_hsa_circ_181847 104377 RMVar_ID_104377 Human_SNP_ID_616429204 m1A Human chr17 - 7497501 7497501 7497501 GAGCATGCTGACTCACACGGGGCAAGCCAGGCAGCTCATTGTCCACCATGGTGGCCACATGGAAC GAGCATGCTGACTCACACGGGGCAAGCCAGGCGGCTCATTGTCCACCATGGTGGCCACATGGAAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7497451..7497525 32194978 MeRIP-seq:(Medium) rs779985380 Functional Loss SNV dbSNP153 33..33 33 - - - 104378 RMVar_ID_104378 Human_SNP_ID_616434354 m1A Human chr17 + 7511473 7511473 7511473 GAAGATCATCATCACGGAGGATGGGGAATTCAAGGCCCTGCAGGAGTGGATCCTGGAGACGGACG GAAGATCATCATCACGGAGGATGGGGAATTCAGGGCCCTGCAGGAGTGGATCCTGGAGACGGACG A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7511426..7511500 26863196 MeRIP-seq:(Medium) rs1319381054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51114,Human_RBP_ID_238458,Human_RBP_ID_768790,Human_RBP_ID_1010599,Human_RBP_ID_1869433,Human_RBP_ID_3547243,Human_RBP_ID_5114528,Human_RBP_ID_5441929,Human_RBP_ID_6644916,Human_RBP_ID_8091531,Human_RBP_ID_8463471,Human_RBP_ID_8822448,Human_RBP_ID_9257752,Human_RBP_ID_9288742,Human_RBP_ID_17262013,Human_RBP_ID_17901144,Human_RBP_ID_23114370,Human_RBP_ID_26331196,Human_RBP_ID_26971675 Human_Splice_Rec_1772432 Human_miRNA_ID_2574515,Human_miRNA_ID_2709023 RMVar_hsa_circ_101531,RMVar_hsa_circ_181846,RMVar_hsa_circ_121436,RMVar_hsa_circ_124249,RMVar_hsa_circ_101116,RMVar_hsa_circ_181852,RMVar_hsa_circ_181853,RMVar_hsa_circ_181851,RMVar_hsa_circ_181857,RMVar_hsa_circ_86656,RMVar_hsa_circ_102663,RMVar_hsa_circ_100329,RMVar_hsa_circ_181859,RMVar_hsa_circ_181858,RMVar_hsa_circ_266729,RMVar_hsa_circ_88562,RMVar_hsa_circ_28373,RMVar_hsa_circ_181874,RMVar_hsa_circ_347616,RMVar_hsa_circ_49315,RMVar_hsa_circ_22501,RMVar_hsa_circ_31595,RMVar_hsa_circ_43857 104379 RMVar_ID_104379 Human_SNP_ID_616434747 m1A Human chr17 + 7512545 7512545 7512545 TGGGTGGAATCTCTCCTGCCATGACACCTTGGAACCAGGGTGCAACCCCTGCCTATGGCGCCTGG TGGGTGGAATCTCTCCTGCCATGACACCTTGGGACCAGGGTGCAACCCCTGCCTATGGCGCCTGG A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7512495..7512878 32194978 MeRIP-seq:(Medium) rs1333395070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526174 Human_Splice_Rec_1772438,Human_Splice_Rec_1772439 RMVar_hsa_circ_101116,RMVar_hsa_circ_181851,RMVar_hsa_circ_181857,RMVar_hsa_circ_86656,RMVar_hsa_circ_100329,RMVar_hsa_circ_181858,RMVar_hsa_circ_49315 104380 RMVar_ID_104380 Human_SNP_ID_616434748 m1A Human chr17 + 7512545 7512545 7512545 TGGGTGGAATCTCTCCTGCCATGACACCTTGGAACCAGGGTGCAACCCCTGCCTATGGCGCCTGG TGGGTGGAATCTCTCCTGCCATGACACCTTGGTACCAGGGTGCAACCCCTGCCTATGGCGCCTGG A T POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7512495..7512878 32194978 MeRIP-seq:(Medium) rs1333395070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5526174 Human_Splice_Rec_1772438,Human_Splice_Rec_1772439 RMVar_hsa_circ_101116,RMVar_hsa_circ_181851,RMVar_hsa_circ_181857,RMVar_hsa_circ_86656,RMVar_hsa_circ_100329,RMVar_hsa_circ_181858,RMVar_hsa_circ_49315 104381 RMVar_ID_104381 Human_SNP_ID_616435021 m1A Human chr17 + 7513199 7513178 7513199 AACTATAGTCCCACATCACCCAGCTATTCGCCAACGTCACCCAGCTACTCACCGACCTCTCCCAG AACTATAGTCCC_____________________ACGTCACCCAGCTACTCACCGACCTCTCCCAG CACATCACCCAGCTATTCGCCA C POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7512877..7513475 26863196 MeRIP-seq:(Medium) rs759016969 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_51122,Human_RBP_ID_135212,Human_RBP_ID_5129057,Human_RBP_ID_5318242,Human_RBP_ID_6644928,Human_RBP_ID_17079463,Human_RBP_ID_17262018,Human_RBP_ID_18941339,Human_RBP_ID_20291807,Human_RBP_ID_22806799 104382 RMVar_ID_104382 Human_SNP_ID_616435025 m1A Human chr17 + 7513192 7513192 7513192 CAGTCCCAACTATAGTCCCACATCACCCAGCTATTCGCCAACGTCACCCAGCTACTCACCGACCT CAGTCCCAACTATAGTCCCACATCACCCAGCTGTTCGCCAACGTCACCCAGCTACTCACCGACCT A G POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7513093..7513525 26863196 MeRIP-seq:(Medium) rs763004366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51122,Human_RBP_ID_135212,Human_RBP_ID_1869441,Human_RBP_ID_5129057,Human_RBP_ID_5318242,Human_RBP_ID_17079463,Human_RBP_ID_17262018,Human_RBP_ID_17377648,Human_RBP_ID_18941339,Human_RBP_ID_20291807,Human_RBP_ID_22806799,Human_RBP_ID_24481109 104383 RMVar_ID_104383 Human_SNP_ID_616435152 m1A Human chr17 - 7513352 7513352 7513352 GAGTAGCTGGGAGATGTCGGCGAGTAGCTGGGAGACGTTGGCGAGTAGCTAGGGGAAGTGGGCGA GAGTAGCTGGGAGATGTCGGCGAGTAGCTGGGGGACGTTGGCGAGTAGCTAGGGGAAGTGGGCGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7513001..7514075 26863410 MeRIP-seq:(Medium) rs1410784004 Functional Loss SNV dbSNP153 33..33 33 - - - 104384 RMVar_ID_104384 Human_SNP_ID_616435153 m1A Human chr17 - 7513352 7513352 7513352 GAGTAGCTGGGAGATGTCGGCGAGTAGCTGGGAGACGTTGGCGAGTAGCTAGGGGAAGTGGGCGA GAGTAGCTGGGAGATGTCGGCGAGTAGCTGGGTGACGTTGGCGAGTAGCTAGGGGAAGTGGGCGA T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7513001..7514075 26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 104385 RMVar_ID_104385 Human_SNP_ID_616435263 m1A Human chr17 - 7513571 7513571 7513571 CTGGTAGGTGTGTAGTTGGGACTAGTAGGTGAATAGCTGGGTGATGTCGGGCTGTAGCTGGGTGA CTGGTAGGTGTGTAGTTGGGACTAGTAGGTGAGTAGCTGGGTGATGTCGGGCTGTAGCTGGGTGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7513551..7513575 26863196 MeRIP-seq:(Medium) rs1362516911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181878 104386 RMVar_ID_104386 Human_SNP_ID_616435320 m1A Human chr17 + 7513700 7513698 7513701 CCAAGTTACTCCCCTTCCAGCCCACGATACACACCACAGTCTCCAACCTATACCCCAAGCTCACC CCAAGTTACTCCCCTTCCAGCCCACGATACA___CACAGTCTCCAACCTATACCCCAAGCTCACC ACAC A POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7513651..7513700 26863196 MeRIP-seq:(Medium) rs1308406058 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_238469,Human_RBP_ID_500338,Human_RBP_ID_3537612,Human_RBP_ID_5129470,Human_RBP_ID_8463481,Human_RBP_ID_17079467,Human_RBP_ID_17262031,Human_RBP_ID_17377659,Human_RBP_ID_18941345,Human_RBP_ID_23171822 Human_miRNA_ID_3086593 104387 RMVar_ID_104387 Human_SNP_ID_616435352 m1A Human chr17 + 7513778 7513777 7513779 AGCTCGCCCAGCTACAGCCCAACCTCACCCACAAGTACACCCCAACCAGTCCTTCTTACAGTCCC AGCTCGCCCAGCTACAGCCCAACCTCACCCAC__GTACACCCCAACCAGTCCTTCTTACAGTCCC CAA C POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:7513001..7514306;chr17:7513024..7514162;chr17:7513024..7514130;chr17:7513051..7514131 26863196 MeRIP-seq:(Medium) rs1247588002 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17079468,Human_RBP_ID_17494872 104388 RMVar_ID_104388 Human_SNP_ID_616435386 m1A Human chr17 - 7513867 7513867 7513867 CTGGTAGGCGAGTACTTGGGAGAGGTGGGTGAATATTTGGGACTGGTAGGTGAGTACTTGGGAGA CTGGTAGGCGAGTACTTGGGAGAGGTGGGTGAGTATTTGGGACTGGTAGGTGAGTACTTGGGAGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7513758..7514173 26863196 MeRIP-seq:(Medium) rs762879160 Functional Loss SNV dbSNP153 33..33 33 - - - 104389 RMVar_ID_104389 Human_SNP_ID_616435478 m1A Human chr17 + 7514072 7514072 7514072 CCACCAGCCCCACCTACTCGCCCACCTCCCCCAAAGGCTCAACCTACTCTCCCACTTCCCCTGGT CCACCAGCCCCACCTACTCGCCCACCTCCCCCCAAGGCTCAACCTACTCTCCCACTTCCCCTGGT A C POLR2A Ensembl:ENSG00000181222 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7514026..7514125 26863196 MeRIP-seq:(Medium) rs1302399671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51123,Human_RBP_ID_238470,Human_RBP_ID_1066797,Human_RBP_ID_5129066,Human_RBP_ID_17079471,Human_RBP_ID_17262039,Human_RBP_ID_17377665,Human_RBP_ID_17495076,Human_RBP_ID_17565520,Human_RBP_ID_18207931,Human_RBP_ID_18942838,Human_RBP_ID_22422001,Human_RBP_ID_22445289,Human_RBP_ID_22957436,Human_RBP_ID_26455418,Human_RBP_ID_27457239 104390 RMVar_ID_104390 Human_SNP_ID_616449587 m1A Human chr17 - 7562095 7562076 7562096 CCAACGCTTCTGGGCCGCGTGCCGCGCCGCCGAGCACCCCGCCGCGCCGCCTCTGGCTCTGCTTC CCAACGCTTCTGGGCCGCGTGCCGCGCCGCC____________________TCTGGCTCTGCTTC AGGCGGCGCGGCGGGGTGCTC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr17:7561921..7563100;chr17:7562001..7563073 26863196,26863410 MeRIP-seq:(Medium) rs532643166 Functional Loss DEL dbSNP153 32..51 33 - - - 104391 RMVar_ID_104391 Human_SNP_ID_616450030 m1A Human chr17 - 7563427 7563427 7563427 CGGCGGCGGCGCTGTGAGCAGGTTTTTCGATGAGTGGGGCGGGAAGGGCGGGGCCGCTGGGAGGT CGGCGGCGGCGCTGTGAGCAGGTTTTTCGATGTGTGGGGCGGGAAGGGCGGGGCCGCTGGGAGGT T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7563326..7563475 26863410 MeRIP-seq:(Medium) rs1411490354 Functional Loss SNV dbSNP153 33..33 33 - - - 104392 RMVar_ID_104392 Human_SNP_ID_616450031 m1A Human chr17 - 7563427 7563427 7563427 CGGCGGCGGCGCTGTGAGCAGGTTTTTCGATGAGTGGGGCGGGAAGGGCGGGGCCGCTGGGAGGT CGGCGGCGGCGCTGTGAGCAGGTTTTTCGATGGGTGGGGCGGGAAGGGCGGGGCCGCTGGGAGGT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7563326..7563475 26863410 MeRIP-seq:(Medium) rs1411490354 Functional Loss SNV dbSNP153 33..33 33 - - - 104393 RMVar_ID_104393 Human_SNP_ID_616450511 m1A Human chr17 + 7564790 7564787 7564790 GCTTTTTCAGGGCTCAGATTTGGGCATGGCAGAAGAGGCAGAGAGGCCTGGGGAGAAAGCCGGCC GCTTTTTCAGGGCTCAGATTTGGGCATGGC___AGAGGCAGAGAGGCCTGGGGAGAAAGCCGGCC CAGA C SENP3,SENP3-EIF4A1 Ensembl:ENSG00000161956,Ensembl:ENSG00000277957 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7564740..7564959 26863196 MeRIP-seq:(Medium) rs765384066 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_48797,Human_RBP_ID_500687,Human_RBP_ID_822831,Human_RBP_ID_4479257,Human_RBP_ID_6646386,Human_RBP_ID_13174304,Human_RBP_ID_18990409 Human_Splice_Rec_1772639,Human_Splice_Rec_1772659,Human_Splice_Rec_1772675,Human_Splice_Rec_1772677,Human_Splice_Rec_1772683,Human_Splice_Rec_1772727 RMVar_hsa_circ_348403,RMVar_hsa_circ_367010,RMVar_hsa_circ_317375,RMVar_hsa_circ_27488,RMVar_hsa_circ_35383 104394 RMVar_ID_104394 Human_SNP_ID_616450524 m1A Human chr17 + 7564826 7564826 7564826 GGCAGAGAGGCCTGGGGAGAAAGCCGGCCAGCACAGCCCCCTGCGAGAGGAGCATGTGACCTGCG GGCAGAGAGGCCTGGGGAGAAAGCCGGCCAGCGCAGCCCCCTGCGAGAGGAGCATGTGACCTGCG A G SENP3,SENP3-EIF4A1 Ensembl:ENSG00000161956,Ensembl:ENSG00000277957 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7564718..7564864 26863196 MeRIP-seq:(Medium) rs758182033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236558,Human_RBP_ID_822831,Human_RBP_ID_4453169,Human_RBP_ID_18990409 Human_Splice_Rec_1772639,Human_Splice_Rec_1772659,Human_Splice_Rec_1772675,Human_Splice_Rec_1772677,Human_Splice_Rec_1772683,Human_Splice_Rec_1772727 RMVar_hsa_circ_348403,RMVar_hsa_circ_367010,RMVar_hsa_circ_317375,RMVar_hsa_circ_27488,RMVar_hsa_circ_35383 104395 RMVar_ID_104395 Human_SNP_ID_616453276 m1A Human chr17 + 7573037 7573020 7573037 GAGGGGGAAGACCCACGGCCGACGCGGCCACCAGGTCGAGGCGGAGGGTAGGGACAGCCCGGCTA GAGGGGGAAGACCCAC_________________GGTCGAGGCGGAGGGTAGGGACAGCCCGGCTA CGGCCGACGCGGCCACCA C SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7572860..7573225 26863196 MeRIP-seq:(Medium) rs1440786933 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_262257,Human_RBP_ID_819572,Human_RBP_ID_3541504,Human_RBP_ID_5098241,Human_RBP_ID_5186066,Human_RBP_ID_5237858,Human_RBP_ID_5318244,Human_RBP_ID_5361561,Human_RBP_ID_5582257,Human_RBP_ID_5649140,Human_RBP_ID_8091886,Human_RBP_ID_8189332,Human_RBP_ID_8232139,Human_RBP_ID_8727037,Human_RBP_ID_9327171,Human_RBP_ID_9422222,Human_RBP_ID_13175626,Human_RBP_ID_18486334,Human_RBP_ID_18941352,Human_RBP_ID_19085842,Human_RBP_ID_24371644,Human_RBP_ID_24559051,Human_RBP_ID_26781112 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885 104396 RMVar_ID_104396 Human_SNP_ID_616453281 m1A Human chr17 + 7573037 7573037 7573037 GAGGGGGAAGACCCACGGCCGACGCGGCCACCAGGTCGAGGCGGAGGGTAGGGACAGCCCGGCTA GAGGGGGAAGACCCACGGCCGACGCGGCCACCGGGTCGAGGCGGAGGGTAGGGACAGCCCGGCTA A G SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7572860..7573225 26863196 MeRIP-seq:(Medium) rs796938099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_262257,Human_RBP_ID_819572,Human_RBP_ID_3541504,Human_RBP_ID_5098241,Human_RBP_ID_5186066,Human_RBP_ID_5237858,Human_RBP_ID_5318244,Human_RBP_ID_5361561,Human_RBP_ID_5582257,Human_RBP_ID_5649140,Human_RBP_ID_8091886,Human_RBP_ID_8189332,Human_RBP_ID_8232139,Human_RBP_ID_8727037,Human_RBP_ID_9327171,Human_RBP_ID_9422222,Human_RBP_ID_13175626,Human_RBP_ID_18486334,Human_RBP_ID_18941352,Human_RBP_ID_19085842,Human_RBP_ID_24371644,Human_RBP_ID_24559051,Human_RBP_ID_26781112 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885 104397 RMVar_ID_104397 Human_SNP_ID_616453409 m1A Human chr17 - 7573319 7573319 7573319 GACCCGTGTTTTAGCCGCGACGAAGTGACTGGATCTAAGGACCAGGCACCCCCGCCTCTCGCGAG GACCCGTGTTTTAGCCGCGACGAAGTGACTGGTTCTAAGGACCAGGCACCCCCGCCTCTCGCGAG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7573317..7573522 26863196 MeRIP-seq:(Medium) rs1171842758 Functional Loss SNV dbSNP153 33..33 33 - - - 104398 RMVar_ID_104398 Human_SNP_ID_616453410 m1A Human chr17 - 7573319 7573319 7573319 GACCCGTGTTTTAGCCGCGACGAAGTGACTGGATCTAAGGACCAGGCACCCCCGCCTCTCGCGAG GACCCGTGTTTTAGCCGCGACGAAGTGACTGGCTCTAAGGACCAGGCACCCCCGCCTCTCGCGAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7573317..7573522 26863196 MeRIP-seq:(Medium) rs1171842758 Functional Loss SNV dbSNP153 33..33 33 - - - 104399 RMVar_ID_104399 Human_SNP_ID_616453445 m1A Human chr17 - 7573384 7573384 7573384 CGGGGTTAGGCTCAGTCCTGGCCGTCAAGAAAACCAGCACACTGAACGGCCGGTTTCTTCTCCCC CGGGGTTAGGCTCAGTCCTGGCCGTCAAGAAATCCAGCACACTGAACGGCCGGTTTCTTCTCCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7573382..7573671 26863196 MeRIP-seq:(Medium) rs1399036485 Functional Loss SNV dbSNP153 33..33 33 - - - 104400 RMVar_ID_104400 Human_SNP_ID_616453835 m1A Human chr17 + 7574255 7574255 7574255 TCGGGCAGGGGACAAAACTTATGCTTTAAACCAACAGATCCAGAGACAATGGCCCCGATGGGATG TCGGGCAGGGGACAAAACTTATGCTTTAAACCGACAGATCCAGAGACAATGGCCCCGATGGGATG A G SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:7574251..7574797;chr17:7574251..7574300 26863196 MeRIP-seq:(Medium) rs370051172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899334,Human_RBP_ID_1543148,Human_RBP_ID_5582142,Human_RBP_ID_13175765,Human_RBP_ID_25347502,Human_RBP_ID_26972250 Human_Splice_Rec_1772747,Human_Splice_Rec_1772767,Human_Splice_Rec_1772777,Human_Splice_Rec_1772781,Human_Splice_Rec_1772805,Human_Splice_Rec_1772811,Human_Splice_Rec_1772819,Human_Splice_Rec_1772827,Human_Splice_Rec_1772843,Human_Splice_Rec_1772869,Human_Splice_Rec_1772885,Human_Splice_Rec_1772893,Human_Splice_Rec_1772911,Human_Splice_Rec_1772921,Human_Splice_Rec_1772935,Human_Splice_Rec_1772955,Human_Splice_Rec_1772969,Human_Splice_Rec_1772987,Human_Splice_Rec_1773001,Human_Splice_Rec_1773007,Human_Splice_Rec_1773011,Human_Splice_Rec_1773019,Human_Splice_Rec_1773023,Human_Splice_Rec_1773077 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885 104401 RMVar_ID_104401 Human_SNP_ID_616454220 m1A Human chr17 + 7575168 7575168 7575168 CAAGCCCAATCTGGGACTGGGAAAACGGCCACATTTGCCATATCGATTCTGCAGCAGATTGAATT CAAGCCCAATCTGGGACTGGGAAAACGGCCACCTTTGCCATATCGATTCTGCAGCAGATTGAATT A C SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA 3'UTR,3'UTR,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7575085..7575203 26863196 MeRIP-seq:(Medium) rs1420564772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500867,Human_RBP_ID_1010746,Human_RBP_ID_1184491,Human_RBP_ID_1543171,Human_RBP_ID_1869789,Human_RBP_ID_3538043,Human_RBP_ID_5188784,Human_RBP_ID_5582322,Human_RBP_ID_6646859,Human_RBP_ID_8464024,Human_RBP_ID_8822638,Human_RBP_ID_9288297,Human_RBP_ID_13175987,Human_RBP_ID_17262110,Human_RBP_ID_17377723,Human_RBP_ID_17494195,Human_RBP_ID_18296654,Human_RBP_ID_18439740,Human_RBP_ID_18709645,Human_RBP_ID_22500534,Human_RBP_ID_24371645,Human_RBP_ID_26811910,Human_RBP_ID_27669754 Human_Splice_Rec_1772750,Human_Splice_Rec_1772751,Human_Splice_Rec_1772770,Human_Splice_Rec_1772771,Human_Splice_Rec_1772784,Human_Splice_Rec_1772785,Human_Splice_Rec_1772808,Human_Splice_Rec_1772814,Human_Splice_Rec_1772822,Human_Splice_Rec_1772823,Human_Splice_Rec_1772830,Human_Splice_Rec_1772831,Human_Splice_Rec_1772834,Human_Splice_Rec_1772835,Human_Splice_Rec_1772846,Human_Splice_Rec_1772847,Human_Splice_Rec_1772856,Human_Splice_Rec_1772857,Human_Splice_Rec_1772872,Human_Splice_Rec_1772878,Human_Splice_Rec_1772888,Human_Splice_Rec_1772889,Human_Splice_Rec_1772896,Human_Splice_Rec_1772897,Human_Splice_Rec_1772904,Human_Splice_Rec_1772905,Human_Splice_Rec_1772914,Human_Splice_Rec_1772915,Human_Splice_Rec_1772938,Human_Splice_Rec_1772939,Human_Splice_Rec_1772958,Human_Splice_Rec_1772959,Human_Splice_Rec_1772972,Human_Splice_Rec_1772973,Human_Splice_Rec_1772990,Human_Splice_Rec_1772991,Human_Splice_Rec_1773004,Human_Splice_Rec_1773010,Human_Splice_Rec_1773014,Human_Splice_Rec_1773015,Human_Splice_Rec_1773022,Human_Splice_Rec_1773026,Human_Splice_Rec_1773027,Human_Splice_Rec_1773039,Human_Splice_Rec_1773080,Human_Splice_Rec_1773081 RMVar_hsa_circ_59937,RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885,RMVar_hsa_circ_181887,RMVar_hsa_circ_120223,RMVar_hsa_circ_369492,RMVar_hsa_circ_181886,RMVar_hsa_circ_338663,RMVar_hsa_circ_105908,RMVar_hsa_circ_339740,RMVar_hsa_circ_372746,RMVar_hsa_circ_343791,RMVar_hsa_circ_111846,RMVar_hsa_circ_100997,RMVar_hsa_circ_181889,RMVar_hsa_circ_181891,RMVar_hsa_circ_181893,RMVar_hsa_circ_36605,RMVar_hsa_circ_181894,RMVar_hsa_circ_181892,RMVar_hsa_circ_181890 104402 RMVar_ID_104402 Human_SNP_ID_616454780 m1A Human chr17 - 7576676 7576676 7576676 GAACCGAATTACTCACACAGGTATCTCCGGTTAAGCATATCAAACACACGGCCAGGGGTACCCAC GAACCGAATTACTCACACAGGTATCTCCGGTTTAGCATATCAAACACACGGCCAGGGGTACCCAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7576512..7576739 26863196 MeRIP-seq:(Medium) rs1567734636 Functional Loss SNV dbSNP153 33..33 33 - - - 104403 RMVar_ID_104403 Human_SNP_ID_616455127 m1A Human chr17 + 7577393 7577393 7577393 CACAATGCCTTCTGATGTGCTTGAGGTGACCAAGAAGTTCATGAGGGACCCCATTCGGATTCTTG CACAATGCCTTCTGATGTGCTTGAGGTGACCATGAAGTTCATGAGGGACCCCATTCGGATTCTTG A T SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA 3'UTR,CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7577324..7577527 26863196 MeRIP-seq:(Medium) rs11552639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500880,Human_RBP_ID_1546956,Human_RBP_ID_3549188,Human_RBP_ID_5098247,Human_RBP_ID_5580703,Human_RBP_ID_9375297,Human_RBP_ID_18709679,Human_RBP_ID_23751026,Human_RBP_ID_26330648 Human_Splice_Rec_1772756,Human_Splice_Rec_1772757,Human_Splice_Rec_1772790,Human_Splice_Rec_1772791,Human_Splice_Rec_1772838,Human_Splice_Rec_1772839,Human_Splice_Rec_1772852,Human_Splice_Rec_1772853,Human_Splice_Rec_1772860,Human_Splice_Rec_1772861,Human_Splice_Rec_1772918,Human_Splice_Rec_1772928,Human_Splice_Rec_1772929,Human_Splice_Rec_1772944,Human_Splice_Rec_1772945,Human_Splice_Rec_1772965,Human_Splice_Rec_1772978,Human_Splice_Rec_1772979,Human_Splice_Rec_1772996,Human_Splice_Rec_1772997,Human_Splice_Rec_1773032,Human_Splice_Rec_1773033,Human_Splice_Rec_1773044,Human_Splice_Rec_1773048,Human_Splice_Rec_1773049,Human_Splice_Rec_1773057,Human_Splice_Rec_1773061,Human_Splice_Rec_1773086,Human_Splice_Rec_1773087 Human_miRNA_ID_245833,Human_miRNA_ID_245834,Human_miRNA_ID_248342,Human_miRNA_ID_248343 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885,RMVar_hsa_circ_105908,RMVar_hsa_circ_343791,RMVar_hsa_circ_111846,RMVar_hsa_circ_100997,RMVar_hsa_circ_18565,RMVar_hsa_circ_181891,RMVar_hsa_circ_181893,RMVar_hsa_circ_181894,RMVar_hsa_circ_181892,RMVar_hsa_circ_181896,RMVar_hsa_circ_101968,RMVar_hsa_circ_103047,RMVar_hsa_circ_181897,RMVar_hsa_circ_110048,RMVar_hsa_circ_370872,RMVar_hsa_circ_375827,RMVar_hsa_circ_121888,RMVar_hsa_circ_77207,RMVar_hsa_circ_117218,RMVar_hsa_circ_181899,RMVar_hsa_circ_181901,RMVar_hsa_circ_181902,RMVar_hsa_circ_181900,RMVar_hsa_circ_370663,RMVar_hsa_circ_181898,RMVar_hsa_circ_374077,RMVar_hsa_circ_369288,RMVar_hsa_circ_181904,RMVar_hsa_circ_181906,RMVar_hsa_circ_89534,RMVar_hsa_circ_181907,RMVar_hsa_circ_181905,RMVar_hsa_circ_181903 104404 RMVar_ID_104404 Human_SNP_ID_616455462 m1A Human chr17 + 7578243 7578243 7578243 ACCTTCCCACCAACAGGGAAAACTATATCCACAGGTAAGCGTAGATCTGGAACACTCCCCTACCC ACCTTCCCACCAACAGGGAAAACTATATCCACCGGTAAGCGTAGATCTGGAACACTCCCCTACCC A C SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA 3'UTR,CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7578235..7578361 26863196 MeRIP-seq:(Medium) rs772196542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1543239,Human_RBP_ID_1869829,Human_RBP_ID_3538077,Human_RBP_ID_8464067,Human_RBP_ID_19078300 Human_Splice_Rec_1772762,Human_Splice_Rec_1772763,Human_Splice_Rec_1772796,Human_Splice_Rec_1772797,Human_Splice_Rec_1772863,Human_Splice_Rec_1772931,Human_Splice_Rec_1772950,Human_Splice_Rec_1772951,Human_Splice_Rec_1773037,Human_Splice_Rec_1773054,Human_Splice_Rec_1773055,Human_Splice_Rec_1773069 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_181881,RMVar_hsa_circ_181885,RMVar_hsa_circ_105908,RMVar_hsa_circ_100997,RMVar_hsa_circ_181893,RMVar_hsa_circ_181894,RMVar_hsa_circ_181896,RMVar_hsa_circ_101968,RMVar_hsa_circ_110048,RMVar_hsa_circ_77207,RMVar_hsa_circ_117218,RMVar_hsa_circ_181901,RMVar_hsa_circ_181902,RMVar_hsa_circ_181906,RMVar_hsa_circ_89534,RMVar_hsa_circ_181907,RMVar_hsa_circ_100405,RMVar_hsa_circ_181910 104405 RMVar_ID_104405 Human_SNP_ID_616455616 m1A Human chr17 + 7578650 7578650 7578650 TGAGGCAAAAGAAGGAACCGTGAACATTTTAGACACCCTTTTCTTTGGGGTAGGCTCTTGCCCCA TGAGGCAAAAGAAGGAACCGTGAACATTTTAGGCACCCTTTTCTTTGGGGTAGGCTCTTGCCCCA A G SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA 3'UTR,3'UTR,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7578556..7578650 26863410 MeRIP-seq:(Medium) rs1410595208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500908,Human_RBP_ID_1543244,Human_RBP_ID_1869832,Human_RBP_ID_2523438,Human_RBP_ID_3538080,Human_RBP_ID_4479427,Human_RBP_ID_5114534,Human_RBP_ID_5581793,Human_RBP_ID_6646946,Human_RBP_ID_8464072,Human_RBP_ID_13176156,Human_RBP_ID_17262122,Human_RBP_ID_17901511,Human_RBP_ID_20272439,Human_RBP_ID_22807014,Human_RBP_ID_22961740,Human_RBP_ID_23209813,Human_RBP_ID_24481262,Human_RBP_ID_25327311,Human_RBP_ID_26455616,Human_RBP_ID_26646275,Human_RBP_ID_27260364 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_181881,RMVar_hsa_circ_181885,RMVar_hsa_circ_105908,RMVar_hsa_circ_181894,RMVar_hsa_circ_181896,RMVar_hsa_circ_101968,RMVar_hsa_circ_77207,RMVar_hsa_circ_117218,RMVar_hsa_circ_181902,RMVar_hsa_circ_181907,RMVar_hsa_circ_100405,RMVar_hsa_circ_102719,RMVar_hsa_circ_181910,RMVar_hsa_circ_181911 104406 RMVar_ID_104406 Human_SNP_ID_616456259 m1A Human chr17 + 7580049 7580049 7580049 ATGGAAACGTCACAGTTCATCCAACAAGCAATAGCACTGCCACCAGCCAGGGACCCTCAACTGCC ATGGAAACGTCACAGTTCATCCAACAAGCAATGGCACTGCCACCAGCCAGGGACCCTCAACTGCC A G AC016876.3,CD68 Ensembl:ENSG00000264772,Ensembl:ENSG00000129226 lincRNA,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7579999..7580117 26863196 MeRIP-seq:(Medium) rs62059825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132608,Human_RBP_ID_901871,Human_RBP_ID_1546963,Human_RBP_ID_17262673,Human_RBP_ID_17378629 Human_miRNA_ID_3152798,Human_miRNA_ID_3152924,Human_miRNA_ID_3169223,Human_miRNA_ID_3176887,Human_miRNA_ID_3177155,Human_miRNA_ID_3187207,Human_miRNA_ID_3187346,Human_miRNA_ID_3207002 104407 RMVar_ID_104407 Human_SNP_ID_616456264 m1A Human chr17 - 7580054 7580054 7580054 TGAGTGGCAGTTGAGGGTCCCTGGCTGGTGGCAGTGCTATTGCTTGTTGGATGAACTGTGACGTT TGAGTGGCAGTTGAGGGTCCCTGGCTGGTGGCCGTGCTATTGCTTGTTGGATGAACTGTGACGTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7579869..7580190 26863196 MeRIP-seq:(Medium) rs749259856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6646965,Human_RBP_ID_23751056 104408 RMVar_ID_104408 Human_SNP_ID_616456345 m1A Human chr17 + 7580250 7580250 7580250 CCAAGGAGACCATTGGAGACTACACGTGGACCAATGGTTCCCAGCCCTGTGTCCACCTCCAAGCC CCAAGGAGACCATTGGAGACTACACGTGGACCGATGGTTCCCAGCCCTGTGTCCACCTCCAAGCC A G AC016876.3,CD68 Ensembl:ENSG00000264772,Ensembl:ENSG00000129226 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7580199..7580486 32194978 MeRIP-seq:(Medium) rs1268328041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22760698 Human_Splice_Rec_1773089,Human_Splice_Rec_1773099,Human_Splice_Rec_1773109,Human_Splice_Rec_1773113 Human_miRNA_ID_3151909,Human_miRNA_ID_3151963 104409 RMVar_ID_104409 Human_SNP_ID_616456539 m1A Human chr17 + 7580760 7580760 7580760 TGTCTACCTGAGCTACATGGCGGTGGAGTACAATGTGTCCTTCCCCCACGCAGCACGTAAGTAAC TGTCTACCTGAGCTACATGGCGGTGGAGTACAGTGTGTCCTTCCCCCACGCAGCACGTAAGTAAC A G AC016876.3,CD68 Ensembl:ENSG00000264772,Ensembl:ENSG00000129226 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7580584..7580921 32194978 MeRIP-seq:(Medium) rs536194152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1773092,Human_Splice_Rec_1773093,Human_Splice_Rec_1773102,Human_Splice_Rec_1773103,Human_Splice_Rec_1773116,Human_Splice_Rec_1773117,Human_Splice_Rec_1773122,Human_Splice_Rec_1773123 Human_miRNA_ID_91341,Human_miRNA_ID_1321730,Human_miRNA_ID_3147613,Human_miRNA_ID_3205818,Human_miRNA_ID_3206277,Human_miRNA_ID_3206523 RMVar_hsa_circ_12977,RMVar_hsa_circ_24065 104410 RMVar_ID_104410 Human_SNP_ID_616457141 m1A Human chr17 + 7582322 7582322 7582322 CAGTTCCCCATCCGTGGCAAGCCGGTAGAGCCATTCATCCCCGCAGCCTTCTTCCTGACCCTCGT CAGTTCCCCATCCGTGGCAAGCCGGTAGAGCCCTTCATCCCCGCAGCCTTCTTCCTGACCCTCGT A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7582215..7582340 26863196 MeRIP-seq:(Medium) rs1404227191 Functional Loss SNV dbSNP153 33..33 33 - - - 104411 RMVar_ID_104411 Human_SNP_ID_616457534 m1A Human chr17 - 7583580 7583580 7583580 ACGCCTTTGTTGACGCTTCCAGTTTGGAAGCCAGATTTACACCCCTGCCTTTCTCCGCTCCTCCT ACGCCTTTGTTGACGCTTCCAGTTTGGAAGCCGGATTTACACCCCTGCCTTTCTCCGCTCCTCCT T C AC016876.2 Ensembl:ENSG00000233223 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7583561..7583729 26863196 MeRIP-seq:(Medium) rs1302005740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254376 104412 RMVar_ID_104412 Human_SNP_ID_616458632 m1A Human chr17 - 7587019 7587019 7587019 CCACAACATCTTGTCCCTTGCTCCTGGTACCCACCCTCCCCACCACCACAGCAGGCACATTGGAG CCACAACATCTTGTCCCTTGCTCCTGGTACCCGCCCTCCCCACCACCACAGCAGGCACATTGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7586947..7587047 32194978 MeRIP-seq:(Medium) rs1359580583 Functional Loss SNV dbSNP153 33..33 33 - - - 104413 RMVar_ID_104413 Human_SNP_ID_616459024 m1A Human chr17 - 7588001 7587973 7588001 CCTTCCCCCACCCCAGCACTGGGGTCCGGGAGACAGTCCCAGCCGGGCTGAGGGAGGGAGGCAGC CCTTCCCCCACCCCAGCACTGGGGTCCGGGAG____________________________GCAGC CCTCCCTCCCTCAGCCCGGCTGGGACTGT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7587951..7588150 26863196 MeRIP-seq:(Medium) rs1323909948 Functional Loss DEL dbSNP153 33..60 33 - - - 104414 RMVar_ID_104414 Human_SNP_ID_616460629 m1A Human chr17 + 7592732 7592732 7592732 CATTCTCTGTCATGTTGGGCCCATCTGATTCCAGGCCTCCATCCATGACGGTCCTGTCTTCATCA CATTCTCTGTCATGTTGGGCCCATCTGATTCCGGGCCTCCATCCATGACGGTCCTGTCTTCATCA A G MPDU1 Ensembl:ENSG00000129255 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7592590..7592789 32194978 MeRIP-seq:(Medium) rs1229750669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27457549 104415 RMVar_ID_104415 Human_SNP_ID_616460955 m1A Human chr17 - 7593495 7593495 7593495 TGGCAGCGACAAGGCTGGATATAGCACTGATGAGAGCTCCTCCTCCTCCCTCCATGCGACTCGAA TGGCAGCGACAAGGCTGGATATAGCACTGATGGGAGCTCCTCCTCCTCCCTCCATGCGACTCGAA T C FXR2 Ensembl:ENSG00000129245 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7593377..7593625 26863196 MeRIP-seq:(Medium) rs1175185649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500979,Human_RBP_ID_3538103,Human_RBP_ID_8464166,Human_RBP_ID_8822703 Human_Splice_Rec_1773387 Human_miRNA_ID_846442,Human_miRNA_ID_1369852 RMVar_hsa_circ_45379 104416 RMVar_ID_104416 Human_SNP_ID_616461169 m1A Human chr17 + 7594287 7594285 7594288 TCTTGTCATTATCACCTTCCACTCGAACCCTCACCACACCAGATTTATCCACAATCTCCTGGATC TCTTGTCATTATCACCTTCCACTCGAACCCT___CACACCAGATTTATCCACAATCTCCTGGATC TCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7594181..7594378 26863196 MeRIP-seq:(Medium) rs1475259675 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1289120 104417 RMVar_ID_104417 Human_SNP_ID_616461170 m1A Human chr17 + 7594295 7594295 7594295 TTATCACCTTCCACTCGAACCCTCACCACACCAGATTTATCCACAATCTCCTGGATCACTTTCCC TTATCACCTTCCACTCGAACCCTCACCACACCCGATTTATCCACAATCTCCTGGATCACTTTCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7594196..7594374 26863196 MeRIP-seq:(Medium) rs1157722066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1289120,Human_RBP_ID_3538105 104418 RMVar_ID_104418 Human_SNP_ID_616461509 m1A Human chr17 - 7595919 7595919 7595919 TGCGAGAGGACCTGATGGGACTGGCAATTGGGACTCACGGTGCCAACATCCAGCAGGCCCGAAAA TGCGAGAGGACCTGATGGGACTGGCAATTGGGCCTCACGGTGCCAACATCCAGCAGGCCCGAAAA T G FXR2 Ensembl:ENSG00000129245 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7595868..7595946 26863196 MeRIP-seq:(Medium) rs779614427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47797,Human_RBP_ID_1869857,Human_RBP_ID_3538108,Human_RBP_ID_5420536,Human_RBP_ID_5467072,Human_RBP_ID_5497891,Human_RBP_ID_6647009,Human_RBP_ID_8822711,Human_RBP_ID_9288350,Human_RBP_ID_13176410,Human_RBP_ID_26332834 Human_Splice_Rec_1773378,Human_Splice_Rec_1773379,Human_Splice_Rec_1773404,Human_Splice_Rec_1773405,Human_Splice_Rec_1773407 Human_miRNA_ID_1987029,Human_miRNA_ID_3123548 RMVar_hsa_circ_90414,RMVar_hsa_circ_82230,RMVar_hsa_circ_113183,RMVar_hsa_circ_181917,RMVar_hsa_circ_181918,RMVar_hsa_circ_321940,RMVar_hsa_circ_333622,RMVar_hsa_circ_181919,RMVar_hsa_circ_181920 104419 RMVar_ID_104419 Human_SNP_ID_616462939 m1A Human chr17 - 7601514 7601514 7601514 TTCCCACTGGTTTCCTCCCAGTCAACCACAGAAGCCCCTGTGAAGCGAGCATCTCTGCTGGGTGA TTCCCACTGGTTTCCTCCCAGTCAACCACAGAGGCCCCTGTGAAGCGAGCATCTCTGCTGGGTGA T C FXR2 Ensembl:ENSG00000129245 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7601362..7601568 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_899337,Human_RBP_ID_22655803 Human_Splice_Rec_1773376 Human_miRNA_ID_2778226 RMVar_hsa_circ_90414,RMVar_hsa_circ_82230,RMVar_hsa_circ_113183,RMVar_hsa_circ_181917,RMVar_hsa_circ_181918,RMVar_hsa_circ_321940,RMVar_hsa_circ_333622,RMVar_hsa_circ_44555,RMVar_hsa_circ_181919,RMVar_hsa_circ_181920,RMVar_hsa_circ_308830,RMVar_hsa_circ_313464,RMVar_hsa_circ_325535,RMVar_hsa_circ_94560,RMVar_hsa_circ_181921,RMVar_hsa_circ_181922,RMVar_hsa_circ_181923 104420 RMVar_ID_104420 Human_SNP_ID_616466614 m1A Human chr17 + 7614837 7614813 7614837 GCCGCCGCCCCCGCTGCTGCCTCAGTCCCGGGACCCGCTGCTGCCGCTGCCGCTCCACAGCCTCC GCCGCCGCC________________________CCCGCTGCTGCCGCTGCCGCTCCACAGCCTCC CCCCGCTGCTGCCTCAGTCCCGGGA C SHBG Ensembl:ENSG00000129214 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7614451..7614900;chr17:7614426..7614904 26863196 MeRIP-seq:(Medium) rs1164847960 Functional Loss DEL dbSNP153 10..33 33 - - - 104421 RMVar_ID_104421 Human_SNP_ID_616466622 m1A Human chr17 - 7614830 7614830 7614830 GTGGAGCGGCAGCGGCAGCAGCGGGTCCCGGGACTGAGGCAGCAGCGGGGGCGGCGGCGGGCGGA GTGGAGCGGCAGCGGCAGCAGCGGGTCCCGGGGCTGAGGCAGCAGCGGGGGCGGCGGCGGGCGGA T C FXR2 Ensembl:ENSG00000129245 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7614413..7614913;chr17:7614427..7614901 26863196 MeRIP-seq:(Medium) rs1315297346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130952,Human_RBP_ID_236116,Human_RBP_ID_765168,Human_RBP_ID_5441962,Human_RBP_ID_5467077 Human_Splice_Rec_1773413 RMVar_hsa_circ_113183,RMVar_hsa_circ_181918,RMVar_hsa_circ_94560,RMVar_hsa_circ_181923 104422 RMVar_ID_104422 Human_SNP_ID_616470067 m1A Human chr17 + 7627027 7627027 7627027 CCATGTACTGTAGATGAAATAGTATATCCCATAGCCCACCACGCAGGGCCCTGAGAGAGAGAAAA CCATGTACTGTAGATGAAATAGTATATCCCATTGCCCACCACGCAGGGCCCTGAGAGAGAGAAAA A T SHBG Ensembl:ENSG00000129214 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7626979..7627080 32194978 MeRIP-seq:(Medium) rs915723405 Functional Loss SNV dbSNP153 33..33 33 - - - 104423 RMVar_ID_104423 Human_SNP_ID_616470259 m1A Human chr17 + 7627594 7627592 7627594 GTCTTCACCCGAATCAGCCTCAGGATATCTCCACAGTCTCCCTCCTTGGCCTCTCGGATCCGCAC GTCTTCACCCGAATCAGCCTCAGGATATCTC__CAGTCTCCCTCCTTGGCCTCTCGGATCCGCAC CCA C SHBG Ensembl:ENSG00000129214 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7627551..7627625 32194978 MeRIP-seq:(Medium) rs752607797 Functional Loss DEL dbSNP153 32..33 33 - - - 104424 RMVar_ID_104424 Human_SNP_ID_616470358 m1A Human chr17 + 7627770 7627770 7627770 GGGGTGGCGGGAGTCGGGGGGGACGGCGGGGTAGCCGCGGCCTGGTAAGTGGAGCTGGGATTCCG GGGGTGGCGGGAGTCGGGGGGGACGGCGGGGTGGCCGCGGCCTGGTAAGTGGAGCTGGGATTCCG A G SHBG Ensembl:ENSG00000129214 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7627626..7627850 26863410 MeRIP-seq:(Medium) rs116289877 Functional Loss SNV dbSNP153 33..33 33 - - - 104425 RMVar_ID_104425 Human_SNP_ID_616470364 m1A Human chr17 - 7627780 7627780 7627780 CGTACGGCGCCGGAATCCCAGCTCCACTTACCAGGCCGCGGCTACCCCGCCGTCCCCCCCGACTC CGTACGGCGCCGGAATCCCAGCTCCACTTACCGGGCCGCGGCTACCCCGCCGTCCCCCCCGACTC T C SAT2 Ensembl:ENSG00000141504 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7627671..7627823 26863196 MeRIP-seq:(Medium) rs1349723451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237903,Human_RBP_ID_4479531,Human_RBP_ID_5441964 104426 RMVar_ID_104426 Human_SNP_ID_616484954 m1A Human chr17 - 7674892 7674892 7674892 GTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCCTGA GTGGAGTATTTGGATGACAGAAACACTTTTCGTCATAGTGTGGTGGTGCCCTATGAGCCGCCTGA T A TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1800372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501217,Human_RBP_ID_1543366,Human_RBP_ID_1869944,Human_RBP_ID_18296710,Human_RBP_ID_23751550,Human_RBP_ID_27457648 Human_Splice_Rec_1773746,Human_Splice_Rec_1773747,Human_Splice_Rec_1773760,Human_Splice_Rec_1773761,Human_Splice_Rec_1773780,Human_Splice_Rec_1773781,Human_Splice_Rec_1773790,Human_Splice_Rec_1773791,Human_Splice_Rec_1773804,Human_Splice_Rec_1773805,Human_Splice_Rec_1773818,Human_Splice_Rec_1773819,Human_Splice_Rec_1773830,Human_Splice_Rec_1773831,Human_Splice_Rec_1773842,Human_Splice_Rec_1773843,Human_Splice_Rec_1773856,Human_Splice_Rec_1773857,Human_Splice_Rec_1773876,Human_Splice_Rec_1773877,Human_Splice_Rec_1773896,Human_Splice_Rec_1773897,Human_Splice_Rec_1773916,Human_Splice_Rec_1773917,Human_Splice_Rec_1773936,Human_Splice_Rec_1773937,Human_Splice_Rec_1773958,Human_Splice_Rec_1773959,Human_Splice_Rec_1773980,Human_Splice_Rec_1773981,Human_Splice_Rec_1774002,Human_Splice_Rec_1774003,Human_Splice_Rec_1774024,Human_Splice_Rec_1774025,Human_Splice_Rec_1774046,Human_Splice_Rec_1774047,Human_Splice_Rec_1774066,Human_Splice_Rec_1774067,Human_Splice_Rec_1774084,Human_Splice_Rec_1774085,Human_Splice_Rec_1774098,Human_Splice_Rec_1774099,Human_Splice_Rec_1774112,Human_Splice_Rec_1774113,Human_Splice_Rec_1774124 Clinvar_Rec_655 GWAS_ID_13658,GWAS_ID_13659,GWAS_ID_13660,GWAS_ID_13661,GWAS_ID_13662,GWAS_ID_13663,GWAS_ID_13664,GWAS_ID_13665,GWAS_ID_13666,GWAS_ID_13667,GWAS_ID_13668,GWAS_ID_13669,GWAS_ID_13670,GWAS_ID_13671,GWAS_ID_13672 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 104427 RMVar_ID_104427 Human_SNP_ID_616484955 m1A Human chr17 - 7674892 7674892 7674892 GTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCCTGA GTGGAGTATTTGGATGACAGAAACACTTTTCGGCATAGTGTGGTGGTGCCCTATGAGCCGCCTGA T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1800372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501217,Human_RBP_ID_1543366,Human_RBP_ID_1869944,Human_RBP_ID_18296710,Human_RBP_ID_23751550,Human_RBP_ID_27457648 Human_Splice_Rec_1773746,Human_Splice_Rec_1773747,Human_Splice_Rec_1773760,Human_Splice_Rec_1773761,Human_Splice_Rec_1773780,Human_Splice_Rec_1773781,Human_Splice_Rec_1773790,Human_Splice_Rec_1773791,Human_Splice_Rec_1773804,Human_Splice_Rec_1773805,Human_Splice_Rec_1773818,Human_Splice_Rec_1773819,Human_Splice_Rec_1773830,Human_Splice_Rec_1773831,Human_Splice_Rec_1773842,Human_Splice_Rec_1773843,Human_Splice_Rec_1773856,Human_Splice_Rec_1773857,Human_Splice_Rec_1773876,Human_Splice_Rec_1773877,Human_Splice_Rec_1773896,Human_Splice_Rec_1773897,Human_Splice_Rec_1773916,Human_Splice_Rec_1773917,Human_Splice_Rec_1773936,Human_Splice_Rec_1773937,Human_Splice_Rec_1773958,Human_Splice_Rec_1773959,Human_Splice_Rec_1773980,Human_Splice_Rec_1773981,Human_Splice_Rec_1774002,Human_Splice_Rec_1774003,Human_Splice_Rec_1774024,Human_Splice_Rec_1774025,Human_Splice_Rec_1774046,Human_Splice_Rec_1774047,Human_Splice_Rec_1774066,Human_Splice_Rec_1774067,Human_Splice_Rec_1774084,Human_Splice_Rec_1774085,Human_Splice_Rec_1774098,Human_Splice_Rec_1774099,Human_Splice_Rec_1774112,Human_Splice_Rec_1774113,Human_Splice_Rec_1774124 Clinvar_Rec_655 GWAS_ID_13658,GWAS_ID_13659,GWAS_ID_13660,GWAS_ID_13661,GWAS_ID_13662,GWAS_ID_13663,GWAS_ID_13664,GWAS_ID_13665,GWAS_ID_13666,GWAS_ID_13667,GWAS_ID_13668,GWAS_ID_13669,GWAS_ID_13670,GWAS_ID_13671,GWAS_ID_13672 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 104428 RMVar_ID_104428 Human_SNP_ID_616485225 m1A Human chr17 - 7675149 7675143 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGC______GTCCGCGCCATGGCCATCTACAAGCAG CGCGGGT C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) rs1555526166 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 Clinvar_Rec_656 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 104429 RMVar_ID_104429 Human_SNP_ID_616485238 m1A Human chr17 - 7675149 7675149 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGCGCCCGCGTCCGCGCCATGGCCATCTACAAGCAG T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) rs772683278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 Clinvar_Rec_657 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 104430 RMVar_ID_104430 Human_SNP_ID_616485318 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCCAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 104431 RMVar_ID_104431 Human_SNP_ID_616485319 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCGAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 104432 RMVar_ID_104432 Human_SNP_ID_616485320 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCTAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 104433 RMVar_ID_104433 Human_SNP_ID_616485733 m1A Human chr17 - 7676184 7676136 7676184 ACAATGGTTCACTGAAGACCCAGGTCCAGATGAAGCTCCCAGAATGCCAGAGGCTGCTCCCCCCG ACAATGGTTCACTGAAGACCCAGGTCCAGATG_________________________________ GCTGGTGCAGGGGCCACGGGGGGAGCAGCCTCTGGCATTCTGGGAGCTT G TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7676051..7676225 26863196 MeRIP-seq:(Medium) rs1567556432 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_501224,Human_RBP_ID_1010817,Human_RBP_ID_1869946,Human_RBP_ID_3951795,Human_RBP_ID_6647588,Human_RBP_ID_13178641 Human_Splice_Rec_1773742,Human_Splice_Rec_1773756,Human_Splice_Rec_1773776,Human_Splice_Rec_1773872,Human_Splice_Rec_1773892,Human_Splice_Rec_1773912,Human_Splice_Rec_1773932,Human_Splice_Rec_1773954,Human_Splice_Rec_1773976,Human_Splice_Rec_1773998,Human_Splice_Rec_1774020,Human_Splice_Rec_1774042,Human_Splice_Rec_1774062,Human_Splice_Rec_1774082,Human_Splice_Rec_1774120,Human_Splice_Rec_1774130,Human_Splice_Rec_1774138,Human_Splice_Rec_1774148 Clinvar_Rec_661 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 104434 RMVar_ID_104434 Human_SNP_ID_616485790 m1A Human chr17 - 7676201 7676201 7676201 TCCCCGGACGATATTGAACAATGGTTCACTGAAGACCCAGGTCCAGATGAAGCTCCCAGAATGCC TCCCCGGACGATATTGAACAATGGTTCACTGAGGACCCAGGTCCAGATGAAGCTCCCAGAATGCC T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr17:7676151..7676225;chr17:7676150..7676250 26863196,32194978 MeRIP-seq:(Medium) rs574255227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501225,Human_RBP_ID_1869946,Human_RBP_ID_3538266,Human_RBP_ID_3951795,Human_RBP_ID_4454239,Human_RBP_ID_6647588,Human_RBP_ID_13178643 Human_Splice_Rec_1773742,Human_Splice_Rec_1773756,Human_Splice_Rec_1773776,Human_Splice_Rec_1773872,Human_Splice_Rec_1773892,Human_Splice_Rec_1773912,Human_Splice_Rec_1773932,Human_Splice_Rec_1773954,Human_Splice_Rec_1773976,Human_Splice_Rec_1773998,Human_Splice_Rec_1774020,Human_Splice_Rec_1774042,Human_Splice_Rec_1774062,Human_Splice_Rec_1774082,Human_Splice_Rec_1774120,Human_Splice_Rec_1774130,Human_Splice_Rec_1774138,Human_Splice_Rec_1774148 Clinvar_Rec_662 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 104435 RMVar_ID_104435 Human_SNP_ID_616486071 m1A Human chr17 - 7676577 7676577 7676577 TTCCGGGTCACTGCCATGGAGGAGCCGCAGTCAGATCCTAGCGTCGAGCCCCCTCTGAGTCAGGA TTCCGGGTCACTGCCATGGAGGAGCCGCAGTCGGATCCTAGCGTCGAGCCCCCTCTGAGTCAGGA T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7676501..7676625 26863196 MeRIP-seq:(Medium) rs573130482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768584,Human_RBP_ID_4454247,Human_RBP_ID_9375311,Human_RBP_ID_13178651,Human_RBP_ID_22443450 Human_Splice_Rec_1773739,Human_Splice_Rec_1773752,Human_Splice_Rec_1773753,Human_Splice_Rec_1773773,Human_Splice_Rec_1773870,Human_Splice_Rec_1773888,Human_Splice_Rec_1773889,Human_Splice_Rec_1773908,Human_Splice_Rec_1773909,Human_Splice_Rec_1773928,Human_Splice_Rec_1773929,Human_Splice_Rec_1773950,Human_Splice_Rec_1773951,Human_Splice_Rec_1773972,Human_Splice_Rec_1773973,Human_Splice_Rec_1773994,Human_Splice_Rec_1773995,Human_Splice_Rec_1774016,Human_Splice_Rec_1774017,Human_Splice_Rec_1774038,Human_Splice_Rec_1774039,Human_Splice_Rec_1774058,Human_Splice_Rec_1774059,Human_Splice_Rec_1774079,Human_Splice_Rec_1774106,Human_Splice_Rec_1774107,Human_Splice_Rec_1774118,Human_Splice_Rec_1774126,Human_Splice_Rec_1774127,Human_Splice_Rec_1774134,Human_Splice_Rec_1774135,Human_Splice_Rec_1774144,Human_Splice_Rec_1774145 Clinvar_Rec_663,Clinvar_Rec_664 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 104436 RMVar_ID_104436 Human_SNP_ID_616486072 m1A Human chr17 - 7676577 7676577 7676577 TTCCGGGTCACTGCCATGGAGGAGCCGCAGTCAGATCCTAGCGTCGAGCCCCCTCTGAGTCAGGA TTCCGGGTCACTGCCATGGAGGAGCCGCAGTCCGATCCTAGCGTCGAGCCCCCTCTGAGTCAGGA T G TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7676501..7676625 26863196 MeRIP-seq:(Medium) rs573130482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768584,Human_RBP_ID_4454247,Human_RBP_ID_9375311,Human_RBP_ID_13178651,Human_RBP_ID_22443450 Human_Splice_Rec_1773739,Human_Splice_Rec_1773752,Human_Splice_Rec_1773753,Human_Splice_Rec_1773773,Human_Splice_Rec_1773870,Human_Splice_Rec_1773888,Human_Splice_Rec_1773889,Human_Splice_Rec_1773908,Human_Splice_Rec_1773909,Human_Splice_Rec_1773928,Human_Splice_Rec_1773929,Human_Splice_Rec_1773950,Human_Splice_Rec_1773951,Human_Splice_Rec_1773972,Human_Splice_Rec_1773973,Human_Splice_Rec_1773994,Human_Splice_Rec_1773995,Human_Splice_Rec_1774016,Human_Splice_Rec_1774017,Human_Splice_Rec_1774038,Human_Splice_Rec_1774039,Human_Splice_Rec_1774058,Human_Splice_Rec_1774059,Human_Splice_Rec_1774079,Human_Splice_Rec_1774106,Human_Splice_Rec_1774107,Human_Splice_Rec_1774118,Human_Splice_Rec_1774126,Human_Splice_Rec_1774127,Human_Splice_Rec_1774134,Human_Splice_Rec_1774135,Human_Splice_Rec_1774144,Human_Splice_Rec_1774145 Clinvar_Rec_663,Clinvar_Rec_664 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 104437 RMVar_ID_104437 Human_SNP_ID_616489083 m1A Human chr17 + 7687432 7687432 7687432 GTCGTGGAAAGCACGCTCCCAGCCCGAACGCAAAGTGTCCCCGGAGCCCAGCAGCTACCTGCTCC GTCGTGGAAAGCACGCTCCCAGCCCGAACGCACAGTGTCCCCGGAGCCCAGCAGCTACCTGCTCC A C WRAP53 Ensembl:ENSG00000141499 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7687117..7687475 26863196 MeRIP-seq:(Medium) rs574904138 Functional Loss SNV dbSNP153 33..33 33 - - - 104438 RMVar_ID_104438 Human_SNP_ID_616489084 m1A Human chr17 + 7687432 7687432 7687432 GTCGTGGAAAGCACGCTCCCAGCCCGAACGCAAAGTGTCCCCGGAGCCCAGCAGCTACCTGCTCC GTCGTGGAAAGCACGCTCCCAGCCCGAACGCAGAGTGTCCCCGGAGCCCAGCAGCTACCTGCTCC A G WRAP53 Ensembl:ENSG00000141499 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7687117..7687475 26863196 MeRIP-seq:(Medium) rs574904138 Functional Loss SNV dbSNP153 33..33 33 - - - 104439 RMVar_ID_104439 Human_SNP_ID_616489390 m1A Human chr17 - 7688563 7688563 7688563 CTCAGGGATCCGACGCAGAGCTAAAGAAACCCACCTGTGCTTCCCTCCTCTTCTGGGAGTAGGCA CTCAGGGATCCGACGCAGAGCTAAAGAAACCCGCCTGTGCTTCCCTCCTCTTCTGGGAGTAGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7688539..7688640 32194978 MeRIP-seq:(Medium) rs886053517 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_665 104440 RMVar_ID_104440 Human_SNP_ID_616530501 m1A Human chr17 + 7836253 7836253 7836253 CCTGCTCTTTGATGTGCACCAAAACCCTTCCCATTCCTAACGTTTCCTCCTCGTTCGCCCCGGCG CCTGCTCTTTGATGTGCACCAAAACCCTTCCCCTTCCTAACGTTTCCTCCTCGTTCGCCCCGGCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7836157..7836344 26863196 MeRIP-seq:(Medium) rs1323284180 Functional Loss SNV dbSNP153 33..33 33 - - - 104441 RMVar_ID_104441 Human_SNP_ID_616531958 m1A Human chr17 + 7841544 7841541 7841545 AAAAGACCGAGACAGGAGCTAGGCAGACACACAGACAGAGACAGCCCCGCGGAGTCATGTAGACA AAAAGACCGAGACAGGAGCTAGGCAGACAC____ACAGAGACAGCCCCGCGGAGTCATGTAGACA CACAG C KDM6B Ensembl:ENSG00000132510 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7841540..7841654 26863196 MeRIP-seq:(Medium) rs956829710 Functional Loss DEL dbSNP153 31..34 33 - - - 104442 RMVar_ID_104442 Human_SNP_ID_616532338 m1A Human chr17 + 7842552 7842552 7842552 GTTAGTATAGACACCGGGAGTCAGGGAGGGCTATTCTTGCCCCAGAGCGAGAGTGGAGGTGAGAG GTTAGTATAGACACCGGGAGTCAGGGAGGGCTGTTCTTGCCCCAGAGCGAGAGTGGAGGTGAGAG A G KDM6B Ensembl:ENSG00000132510 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7842541..7842937 26863196 MeRIP-seq:(Medium) rs922904374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542625,Human_RBP_ID_8092544 104443 RMVar_ID_104443 Human_SNP_ID_616533230 m1A Human chr17 - 7845022 7845022 7845022 CACTGGGCCGACCCAAAACGCAGCGGCCGCTTACCCGGCCTCCGTGGGAGCGTCCTCACACCGCG CACTGGGCCGACCCAAAACGCAGCGGCCGCTTGCCCGGCCTCCGTGGGAGCGTCCTCACACCGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7844980..7845373 32194978 MeRIP-seq:(Medium) rs1397044160 Functional Loss SNV dbSNP153 33..33 33 - - - 104444 RMVar_ID_104444 Human_SNP_ID_616534380 m1A Human chr17 - 7847248 7847248 7847248 TCTCTAAGGTCACTTCCGGGGGGACGGGTGGCAGGCAGGCAGCCATGGCTCTCTGCTCCTGGGGG TCTCTAAGGTCACTTCCGGGGGGACGGGTGGCGGGCAGGCAGCCATGGCTCTCTGCTCCTGGGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7847200..7847399 32194978 MeRIP-seq:(Medium) rs749080409 Functional Loss SNV dbSNP153 33..33 33 - - - 104445 RMVar_ID_104445 Human_SNP_ID_616534415 m1A Human chr17 + 7847312 7847312 7847312 AGAGCAGAGTTCAGAGGTCGCGGATGGACTCCAGCGTTTCACCAGCAGCAACCACCGCCTGCGTG AGAGCAGAGTTCAGAGGTCGCGGATGGACTCCGGCGTTTCACCAGCAGCAACCACCGCCTGCGTG A G KDM6B Ensembl:ENSG00000132510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:7847150..7848288;chr17:7847304..7847388 26863196 MeRIP-seq:(Medium) rs1406375723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22222428 Human_miRNA_ID_272209,Human_miRNA_ID_2052417 RMVar_hsa_circ_181936,RMVar_hsa_circ_106841,RMVar_hsa_circ_109784,RMVar_hsa_circ_181937,RMVar_hsa_circ_104114,RMVar_hsa_circ_181938 104446 RMVar_ID_104446 Human_SNP_ID_616534651 m1A Human chr17 + 7847689 7847688 7847689 CCCCACCTATCCCTGCCACCTGGACCTTCCTCACCCCCTCCACCCCCCTGTCCCCGCCTCTTACG CCCCACCTATCCCTGCCACCTGGACCTTCCTC_CCCCCTCCACCCCCCTGTCCCCGCCTCTTACG CA C KDM6B Ensembl:ENSG00000132510 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7847640..7847791 32194978 MeRIP-seq:(Medium) rs1208126823 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_501732,Human_RBP_ID_17079473,Human_RBP_ID_18941363,Human_RBP_ID_27458056 RMVar_hsa_circ_181936,RMVar_hsa_circ_106841,RMVar_hsa_circ_109784,RMVar_hsa_circ_181937,RMVar_hsa_circ_126022,RMVar_hsa_circ_181939 104447 RMVar_ID_104447 Human_SNP_ID_616534652 m1A Human chr17 + 7847689 7847689 7847689 CCCCACCTATCCCTGCCACCTGGACCTTCCTCACCCCCTCCACCCCCCTGTCCCCGCCTCTTACG CCCCACCTATCCCTGCCACCTGGACCTTCCTCCCCCCCTCCACCCCCCTGTCCCCGCCTCTTACG A C KDM6B Ensembl:ENSG00000132510 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7847640..7847791 32194978 MeRIP-seq:(Medium) rs771692170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501732,Human_RBP_ID_17079473,Human_RBP_ID_18941363,Human_RBP_ID_27458056 RMVar_hsa_circ_181936,RMVar_hsa_circ_106841,RMVar_hsa_circ_109784,RMVar_hsa_circ_181937,RMVar_hsa_circ_126022,RMVar_hsa_circ_181939 104448 RMVar_ID_104448 Human_SNP_ID_616534838 m1A Human chr17 + 7847936 7847936 7847936 ATTCTCACACCCCTCCCACTCCCCCAACCCCAACCACCAGCAGTAGCAACAGCAACAGTGGCAGC ATTCTCACACCCCTCCCACTCCCCCAACCCCAGCCACCAGCAGTAGCAACAGCAACAGTGGCAGC A G KDM6B Ensembl:ENSG00000132510 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7847889..7848238 32194978 MeRIP-seq:(Medium) rs1361566141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131060,Human_RBP_ID_5129071,Human_RBP_ID_17080508,Human_RBP_ID_17378167,Human_RBP_ID_18942846 Human_miRNA_ID_272211,Human_miRNA_ID_2052419 RMVar_hsa_circ_181936,RMVar_hsa_circ_106841,RMVar_hsa_circ_109784,RMVar_hsa_circ_181937,RMVar_hsa_circ_126022,RMVar_hsa_circ_181939 104449 RMVar_ID_104449 Human_SNP_ID_616535487 m1A Human chr17 - 7849143 7849143 7849143 CAGCCTCCTCCTTGGCCTGTGCGGGGGGCAGCAGTCGCTCAGTCCCACTGTCCGCTGGCTCTGCT CAGCCTCCTCCTTGGCCTGTGCGGGGGGCAGCGGTCGCTCAGTCCCACTGTCCGCTGGCTCTGCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7849098..7849250 26863196 MeRIP-seq:(Medium) rs773586181 Functional Loss SNV dbSNP153 33..33 33 - - - 104450 RMVar_ID_104450 Human_SNP_ID_616535534 m1A Human chr17 + 7849224 7849213 7849225 GTCAGGCAGCTGTAAGCGGCGACAGAAGGAGCATCAGAAGGAGCATCGGCGGCACAGGCGGGCCT GTCAGGCAGCTGTAAGCGGCGA____________CAGAAGGAGCATCGGCGGCACAGGCGGGCCT ACAGAAGGAGCAT A KDM6B Ensembl:ENSG00000132510 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7849050..7849310 26863196 MeRIP-seq:(Medium) rs547582872 Functional Loss DEL dbSNP153,HGVD 23..34 33 - - - RMVar_hsa_circ_181936,RMVar_hsa_circ_106841,RMVar_hsa_circ_109784,RMVar_hsa_circ_181937,RMVar_hsa_circ_126022,RMVar_hsa_circ_181939 104451 RMVar_ID_104451 Human_SNP_ID_616535759 m1A Human chr17 - 7849677 7849677 7849677 CAGCAGCACAGTGGCTGATGGTGAGGTCTGCCATGCGCAGCCGCCGCTCTTCCACCTCAGAGGCG CAGCAGCACAGTGGCTGATGGTGAGGTCTGCCGTGCGCAGCCGCCGCTCTTCCACCTCAGAGGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7849629..7849871 32194978 MeRIP-seq:(Medium) rs1471671568 Functional Loss SNV dbSNP153 33..33 33 - - - 104452 RMVar_ID_104452 Human_SNP_ID_616537387 m1A Human chr17 + 7853862 7853862 7853862 CGGGGGTCACATACGGGTTCCCTCACCCTGCCAGCCGCCCGCCCGCCCGGCGCAGATGCACGCGG CGGGGGTCACATACGGGTTCCCTCACCCTGCCGGCCGCCCGCCCGCCCGGCGCAGATGCACGCGG A G KDM6B Ensembl:ENSG00000132510 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7853825..7853913 26863196 MeRIP-seq:(Medium) rs950600074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501743,Human_RBP_ID_768543 104453 RMVar_ID_104453 Human_SNP_ID_616537524 m1A Human chr17 + 7854200 7854198 7854200 GACCGCCCGTCGCCGGGCTCTCCCCGCGCCCCAGTGTGTGTCCGGGCCCGGCCCGACCGTCTCCA GACCGCCCGTCGCCGGGCTCTCCCCGCGCCC__GTGTGTGTCCGGGCCCGGCCCGACCGTCTCCA CCA C KDM6B Ensembl:ENSG00000132510 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7854151..7854286;chr17:7854166..7854289 26863196 MeRIP-seq:(Medium) rs1567806929 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_501752,Human_RBP_ID_5115061,Human_RBP_ID_24416325 104454 RMVar_ID_104454 Human_SNP_ID_616537525 m1A Human chr17 + 7854200 7854200 7854200 GACCGCCCGTCGCCGGGCTCTCCCCGCGCCCCAGTGTGTGTCCGGGCCCGGCCCGACCGTCTCCA GACCGCCCGTCGCCGGGCTCTCCCCGCGCCCCCGTGTGTGTCCGGGCCCGGCCCGACCGTCTCCA A C KDM6B Ensembl:ENSG00000132510 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7854151..7854286;chr17:7854166..7854289 26863196 MeRIP-seq:(Medium) rs1224282270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501752,Human_RBP_ID_5115061,Human_RBP_ID_24416325 104455 RMVar_ID_104455 Human_SNP_ID_616538824 m1A Human chr17 - 7857152 7857152 7857152 GCGCGAGGACTCGGCGGCTGAGCGCGCCCGACAGCAGCTAGAGGCGCTGCTCAACAAGACTATGC GCGCGAGGACTCGGCGGCTGAGCGCGCCCGACGGCAGCTAGAGGCGCTGCTCAACAAGACTATGC T C NAA38 Ensembl:ENSG00000183011 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:7857051..7857250 26863410 MeRIP-seq:(Medium) rs1024681594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501783,Human_RBP_ID_4455574,Human_RBP_ID_5115065,Human_RBP_ID_9377504,Human_RBP_ID_17902075,Human_RBP_ID_22443453,Human_RBP_ID_27813382 Human_Splice_Rec_1774866,Human_Splice_Rec_1774872,Human_Splice_Rec_1774876,Human_Splice_Rec_1774884 Human_miRNA_ID_1968808,Human_miRNA_ID_2756976 RMVar_hsa_circ_102583,RMVar_hsa_circ_98840,RMVar_hsa_circ_181945,RMVar_hsa_circ_181946 104456 RMVar_ID_104456 Human_SNP_ID_616538843 m1A Human chr17 - 7857176 7857176 7857176 CCCCGCGCAGGATTCGGACGGAGAGCGCGAGGACTCGGCGGCTGAGCGCGCCCGACAGCAGCTAG CCCCGCGCAGGATTCGGACGGAGAGCGCGAGGGCTCGGCGGCTGAGCGCGCCCGACAGCAGCTAG T C NAA38 Ensembl:ENSG00000183011 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7857026..7857250;chr17:7856971..7857275 26863196 MeRIP-seq:(Medium) rs1235804240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237002,Human_RBP_ID_501783,Human_RBP_ID_822248,Human_RBP_ID_4455574,Human_RBP_ID_5115065,Human_RBP_ID_8822945,Human_RBP_ID_9327181,Human_RBP_ID_9377504,Human_RBP_ID_17654090,Human_RBP_ID_17902075,Human_RBP_ID_22443453,Human_RBP_ID_27813382 Human_Splice_Rec_1774866,Human_Splice_Rec_1774872,Human_Splice_Rec_1774876,Human_Splice_Rec_1774884 Human_miRNA_ID_3010861 RMVar_hsa_circ_102583,RMVar_hsa_circ_98840,RMVar_hsa_circ_181945,RMVar_hsa_circ_181946 104457 RMVar_ID_104457 Human_SNP_ID_616538964 m1A Human chr17 + 7857356 7857356 7857356 ACCCCCTCCATCTTGCTGCTTGACTGCCCCTCAGTCCCAGAACCAGAGCCCGTGCTAACCCCAGC ACCCCCTCCATCTTGCTGCTTGACTGCCCCTCGGTCCCAGAACCAGAGCCCGTGCTAACCCCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7857354..7857607 26863196 MeRIP-seq:(Medium) rs779995030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1289285 104458 RMVar_ID_104458 Human_SNP_ID_616539018 m1A Human chr17 + 7857452 7857452 7857452 CCATTCTCTTCTCGTAGCAGCATGGTCGGTCCAGCTCCGGCCATTTGCCCGGAGGCCTCCTCTGG CCATTCTCTTCTCGTAGCAGCATGGTCGGTCCGGCTCCGGCCATTTGCCCGGAGGCCTCCTCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7857344..7857625;chr17:7857349..7857634 26863196 MeRIP-seq:(Medium) rs1457885372 Functional Loss SNV dbSNP153 33..33 33 - - - 104459 RMVar_ID_104459 Human_SNP_ID_616539379 m1A Human chr17 - 7858296 7858290 7858296 ACACTCCGGCCCCGGCCCAACGTGTGGCCCTTACCCTTGTATTCCTGTGCCAATGACGTTAGGTC ACACTCCGGCCCCGGCCCAACGTGTGGCCCTT______GTATTCCTGTGCCAATGACGTTAGGTC CAAGGGT C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7858291..7858391 32194978 MeRIP-seq:(Medium) rs769802563 Functional Loss DEL dbSNP153 33..38 33 - - - Human_Splice_Rec_1774895 104460 RMVar_ID_104460 Human_SNP_ID_616545350 m1A Human chr17 - 7884167 7884167 7884167 TTACACCCCCATCTCCAAGCCTTTACCCAGAAACCCACAAATTTCTCCTTTTTCATAACTGATTA TTACACCCCCATCTCCAAGCCTTTACCCAGAAGCCCACAAATTTCTCCTTTTTCATAACTGATTA T C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7884158..7884252 26863196 MeRIP-seq:(Medium) rs1182444532 Functional Loss SNV dbSNP153 33..33 33 - - - 104461 RMVar_ID_104461 Human_SNP_ID_616545625 m1A Human chr17 + 7884849 7884849 7884849 CTCTGAGGGACGAGGAGGAGGAGGAGGAGGAGATGGTGGTGTCGGAGGAGGAAGAAGAGGAGGAA CTCTGAGGGACGAGGAGGAGGAGGAGGAGGAGGTGGTGGTGTCGGAGGAGGAAGAAGAGGAGGAA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7884800..7885076 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4480043,Human_RBP_ID_5648796,Human_RBP_ID_8190902,Human_RBP_ID_8822971,Human_RBP_ID_9422765 104462 RMVar_ID_104462 Human_SNP_ID_616545626 m1A Human chr17 + 7884849 7884849 7884849 CTCTGAGGGACGAGGAGGAGGAGGAGGAGGAGATGGTGGTGTCGGAGGAGGAAGAAGAGGAGGAA CTCTGAGGGACGAGGAGGAGGAGGAGGAGGAGTTGGTGGTGTCGGAGGAGGAAGAAGAGGAGGAA A T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7884800..7885076 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4480043,Human_RBP_ID_5648796,Human_RBP_ID_8190902,Human_RBP_ID_8822971,Human_RBP_ID_9422765 104463 RMVar_ID_104463 Human_SNP_ID_616545738 m1A Human chr17 - 7885054 7885036 7885054 TACCTGGCGGCGGGGGCGGCGGCGGCGGGGGCAGCGGTGGCGGCGGCGGCGGCGGCGGCGGGAAG TACCTGGCGGCGGGGGCGGCGGCGGCGGGGGC__________________GGCGGCGGCGGGAAG CGCCGCCGCCGCCACCGCT C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7884762..7885159 26863196 MeRIP-seq:(Medium) rs1287703858 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_134356,Human_RBP_ID_26758712 104464 RMVar_ID_104464 Human_SNP_ID_616545755 m1A Human chr17 + 7885049 7885049 7885049 CACCTCTTCCCGCCGCCGCCGCCGCCGCCGCCACCGCTGCCCCCGCCGCCGCCGCCCCCGCCGCC CACCTCTTCCCGCCGCCGCCGCCGCCGCCGCCCCCGCTGCCCCCGCCGCCGCCGCCCCCGCCGCC A C CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr17:7884801..7885157;chr17:7884838..7885155;chr17:7884859..7885291 26863196 MeRIP-seq:(Medium) rs564008487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1774921 104465 RMVar_ID_104465 Human_SNP_ID_616545756 m1A Human chr17 + 7885049 7885049 7885049 CACCTCTTCCCGCCGCCGCCGCCGCCGCCGCCACCGCTGCCCCCGCCGCCGCCGCCCCCGCCGCC CACCTCTTCCCGCCGCCGCCGCCGCCGCCGCCGCCGCTGCCCCCGCCGCCGCCGCCCCCGCCGCC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr17:7884801..7885157;chr17:7884838..7885155;chr17:7884859..7885291 26863196 MeRIP-seq:(Medium) rs564008487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1774921 104466 RMVar_ID_104466 Human_SNP_ID_616545758 m1A Human chr17 - 7885054 7885054 7885054 TACCTGGCGGCGGGGGCGGCGGCGGCGGGGGCAGCGGTGGCGGCGGCGGCGGCGGCGGCGGGAAG TACCTGGCGGCGGGGGCGGCGGCGGCGGGGGCGGCGGTGGCGGCGGCGGCGGCGGCGGCGGGAAG T C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7884762..7885159 26863196 MeRIP-seq:(Medium) rs1419744572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134356,Human_RBP_ID_26758712 104467 RMVar_ID_104467 Human_SNP_ID_616547099 m1A Human chr17 + 7889675 7889675 7889675 CTGATGCTTTTTGCTTCAAAGATAAGGATGACATTCGGCTGCTGCCGTCAGCATTGGGTGTGAAG CTGATGCTTTTTGCTTCAAAGATAAGGATGACTTTCGGCTGCTGCCGTCAGCATTGGGTGTGAAG A T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7889651..7889700 26863196 MeRIP-seq:(Medium) rs759766418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4456233 Human_Splice_Rec_1774922,Human_Splice_Rec_1775000,Human_Splice_Rec_1775012,Human_Splice_Rec_1775062,Human_Splice_Rec_1775064,Human_Splice_Rec_1775142 RMVar_hsa_circ_181950,RMVar_hsa_circ_308021 104468 RMVar_ID_104468 Human_SNP_ID_616547132 m1A Human chr17 - 7889776 7889776 7889776 TTGCCACAGAGTTAGGAATTCTTGACACTTACACGCTTCTTGCGTTTTCGGGGTTTTCCTGGCTT TTGCCACAGAGTTAGGAATTCTTGACACTTACGCGCTTCTTGCGTTTTCGGGGTTTTCCTGGCTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7889726..7889800 26863196 MeRIP-seq:(Medium) rs751355886 Functional Loss SNV dbSNP153 33..33 33 - - - 104469 RMVar_ID_104469 Human_SNP_ID_616547345 m1A Human chr17 - 7890553 7890547 7890553 TTCCTCCTCACTGTCCTAAGAGAAAGAAATAAAAATAACATTTATTCATCCCTACCATTGCCAGA TTCCTCCTCACTGTCCTAAGAGAAAGAAATAA______CATTTATTCATCCCTACCATTGCCAGA GTTATTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:7890551..7890675 26863196 MeRIP-seq:(Medium) rs753823202 Functional Loss DEL dbSNP153,HGVD 33..38 33 - - - 104470 RMVar_ID_104470 Human_SNP_ID_616547396 m1A Human chr17 + 7890662 7890657 7890663 GGGCAGTGAATATGGAACCGGACCGGGTCGGAAACGAAGAAGGAAGCACCGAGAAAAAAAGGAGA GGGCAGTGAATATGGAACCGGACCGGGT______CGAAGAAGGAAGCACCGAGAAAAAAAGGAGA TCGGAAA T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7889629..7894626;chr17:7889618..7894630 26863196 MeRIP-seq:(Medium) rs756760970 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_50852,Human_RBP_ID_4456243,Human_RBP_ID_5577836,Human_RBP_ID_22061017,Human_RBP_ID_22658367,Human_RBP_ID_22957909,Human_RBP_ID_24544770,Human_RBP_ID_26331213,Human_RBP_ID_27458273 Human_Splice_Rec_1774924,Human_Splice_Rec_1774925,Human_Splice_Rec_1775002,Human_Splice_Rec_1775003,Human_Splice_Rec_1775014,Human_Splice_Rec_1775015,Human_Splice_Rec_1775066,Human_Splice_Rec_1775067,Human_Splice_Rec_1775144,Human_Splice_Rec_1775145,Human_Splice_Rec_1775218,Human_Splice_Rec_1775220,Human_Splice_Rec_1775221 RMVar_hsa_circ_181950,RMVar_hsa_circ_308021,RMVar_hsa_circ_276815 104471 RMVar_ID_104471 Human_SNP_ID_616547396 m1A Human chr17 + 7890663 7890657 7890663 GGCAGTGAATATGGAACCGGACCGGGTCGGAAACGAAGAAGGAAGCACCGAGAAAAAAAGGAGAA GGCAGTGAATATGGAACCGGACCGGGT______CGAAGAAGGAAGCACCGAGAAAAAAAGGAGAA TCGGAAA T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:7889609..7891025;chr17:7890503..7890763 26863196 MeRIP-seq:(Medium) rs756760970 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_50852,Human_RBP_ID_22061017,Human_RBP_ID_22658367,Human_RBP_ID_24544770,Human_RBP_ID_27458273 Human_Splice_Rec_1774924,Human_Splice_Rec_1774925,Human_Splice_Rec_1775002,Human_Splice_Rec_1775003,Human_Splice_Rec_1775014,Human_Splice_Rec_1775015,Human_Splice_Rec_1775066,Human_Splice_Rec_1775067,Human_Splice_Rec_1775144,Human_Splice_Rec_1775145,Human_Splice_Rec_1775218,Human_Splice_Rec_1775220,Human_Splice_Rec_1775221 RMVar_hsa_circ_181950,RMVar_hsa_circ_308021,RMVar_hsa_circ_276815 104472 RMVar_ID_104472 Human_SNP_ID_616547399 m1A Human chr17 + 7890666 7890664 7890667 AGTGAATATGGAACCGGACCGGGTCGGAAACGAAGAAGGAAGCACCGAGAAAAAAAGGAGAAGAA AGTGAATATGGAACCGGACCGGGTCGGAAAC___GAAGGAAGCACCGAGAAAAAAAGGAGAAGAA CGAA C CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7890551..7890750 26863196 MeRIP-seq:(Medium) rs771266385 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_22061017,Human_RBP_ID_22658367,Human_RBP_ID_24544770,Human_RBP_ID_27458273 Human_Splice_Rec_1774924,Human_Splice_Rec_1774925,Human_Splice_Rec_1775002,Human_Splice_Rec_1775003,Human_Splice_Rec_1775014,Human_Splice_Rec_1775015,Human_Splice_Rec_1775066,Human_Splice_Rec_1775067,Human_Splice_Rec_1775144,Human_Splice_Rec_1775145,Human_Splice_Rec_1775218,Human_Splice_Rec_1775220,Human_Splice_Rec_1775221 RMVar_hsa_circ_181950,RMVar_hsa_circ_308021,RMVar_hsa_circ_276815 104473 RMVar_ID_104473 Human_SNP_ID_616548183 m1A Human chr17 - 7893501 7893501 7893501 GGGGCTGGATATCAGCAGCAGGGGGTGGTGGAAGGGCGGGGGGTCCGGAGGGTGCTATGGGGGTG GGGGCTGGATATCAGCAGCAGGGGGTGGTGGAGGGGCGGGGGGTCCGGAGGGTGCTATGGGGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7893451..7893550 26863196 MeRIP-seq:(Medium) rs749149678 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 104474 RMVar_ID_104474 Human_SNP_ID_616548295 m1A Human chr17 + 7893839 7893839 7893839 CCAGGCCATAAGAGGCGGAGTAAGAGCCCCCGAGTGCCTGATGGACGCAAGAAGCTTCGGGGAAA CCAGGCCATAAGAGGCGGAGTAAGAGCCCCCGGGTGCCTGATGGACGCAAGAAGCTTCGGGGAAA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7893826..7893850 26863196 MeRIP-seq:(Medium) rs1283934172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1774930,Human_Splice_Rec_1774931,Human_Splice_Rec_1775008,Human_Splice_Rec_1775009,Human_Splice_Rec_1775020,Human_Splice_Rec_1775021,Human_Splice_Rec_1775072,Human_Splice_Rec_1775073,Human_Splice_Rec_1775150,Human_Splice_Rec_1775151,Human_Splice_Rec_1775226,Human_Splice_Rec_1775227,Human_Splice_Rec_1775240,Human_Splice_Rec_1775241,Human_Splice_Rec_1775245 104475 RMVar_ID_104475 Human_SNP_ID_616548305 m1A Human chr17 + 7893856 7893856 7893856 GAGTAAGAGCCCCCGAGTGCCTGATGGACGCAAGAAGCTTCGGGGAAAGAAAATGGCACCACTCA GAGTAAGAGCCCCCGAGTGCCTGATGGACGCAGGAAGCTTCGGGGAAAGAAAATGGCACCACTCA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7893806..7893949 26863196 MeRIP-seq:(Medium) rs761263308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8465063,Human_RBP_ID_26331219 Human_Splice_Rec_1774930,Human_Splice_Rec_1774931,Human_Splice_Rec_1775008,Human_Splice_Rec_1775009,Human_Splice_Rec_1775020,Human_Splice_Rec_1775021,Human_Splice_Rec_1775072,Human_Splice_Rec_1775073,Human_Splice_Rec_1775150,Human_Splice_Rec_1775151,Human_Splice_Rec_1775226,Human_Splice_Rec_1775227,Human_Splice_Rec_1775240,Human_Splice_Rec_1775241,Human_Splice_Rec_1775245 104476 RMVar_ID_104476 Human_SNP_ID_616548580 m1A Human chr17 + 7894594 7894594 7894594 CTGAGCTTGACCGGGCTCCAGAGGGCAAATGGAGCTGCCCTCACTGTGTGAGTACCTAATGCCAG CTGAGCTTGACCGGGCTCCAGAGGGCAAATGGGGCTGCCCTCACTGTGTGAGTACCTAATGCCAG A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7894395..7894625 26863196 MeRIP-seq:(Medium) rs1243593596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8824418,Human_RBP_ID_9377507,Human_RBP_ID_26973208,Human_RBP_ID_27813389 Human_Splice_Rec_1774935,Human_Splice_Rec_1775025,Human_Splice_Rec_1775077,Human_Splice_Rec_1775155,Human_Splice_Rec_1775231,Human_Splice_Rec_1775249 104477 RMVar_ID_104477 Human_SNP_ID_616548714 m1A Human chr17 + 7894993 7894993 7894993 ATACGAAGAGGAGGGAGAGGAAGAAGGGGAGAAGGAGGAGGAGGATGATCACATGGAGTACTGCC ATACGAAGAGGAGGGAGAGGAAGAAGGGGAGAGGGAGGAGGAGGATGATCACATGGAGTACTGCC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7894976..7895000 26863196 MeRIP-seq:(Medium) rs375906970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50856,Human_RBP_ID_896179,Human_RBP_ID_18411986,Human_RBP_ID_26331223,Human_RBP_ID_26973213,Human_RBP_ID_27812244 Human_Splice_Rec_1774936,Human_Splice_Rec_1775026,Human_Splice_Rec_1775078,Human_Splice_Rec_1775156,Human_Splice_Rec_1775232,Human_Splice_Rec_1775250 104478 RMVar_ID_104478 Human_SNP_ID_616548830 m1A Human chr17 + 7895401 7895401 7895401 ATCCTACATTGGCGGTGGGGGGAGCCACCTGTAGCAGTGCCAGCCCCTCAACAGGCAGATGGAAA ATCCTACATTGGCGGTGGGGGGAGCCACCTGTGGCAGTGCCAGCCCCTCAACAGGCAGATGGAAA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:7895326..7895450;chr17:7895319..7895447 26863196 MeRIP-seq:(Medium) rs746192275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_898259,Human_RBP_ID_9289817,Human_RBP_ID_17902306 Human_Splice_Rec_1774938,Human_Splice_Rec_1775028,Human_Splice_Rec_1775080,Human_Splice_Rec_1775158,Human_Splice_Rec_1775234,Human_Splice_Rec_1775252 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951 104479 RMVar_ID_104479 Human_SNP_ID_616549363 m1A Human chr17 + 7897189 7897189 7897189 CTATGGCTCCGGCGAGGATGATGGGAAGAGCGACAAGCGTAAAGTGAAAGACCCGCACTATGCTG CTATGGCTCCGGCGAGGATGATGGGAAGAGCGGCAAGCGTAAAGTGAAAGACCCGCACTATGCTG A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7894774..7897275 32194978 MeRIP-seq:(Medium) rs767237031 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4456350,Human_RBP_ID_18710560,Human_RBP_ID_26331225,Human_RBP_ID_27813392 RMVar_hsa_circ_181956,RMVar_hsa_circ_103898,RMVar_hsa_circ_120719,RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_290346,RMVar_hsa_circ_109586,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_92465,RMVar_hsa_circ_181958,RMVar_hsa_circ_181960,RMVar_hsa_circ_29277,RMVar_hsa_circ_181959,RMVar_hsa_circ_181957,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953 104480 RMVar_ID_104480 Human_SNP_ID_616549690 m1A Human chr17 + 7898567 7898567 7898567 GTATAAGAAGAAGAAGAAGGAGCTACAGGGTGATGGGCCTCCCAGTTCTCCCACTAATGATGTGA GTATAAGAAGAAGAAGAAGGAGCTACAGGGTGGTGGGCCTCCCAGTTCTCCCACTAATGATGTGA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7898516..7899032 32194978 MeRIP-seq:(Medium) rs1250591178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8824421,Human_RBP_ID_9288770,Human_RBP_ID_18990442,Human_RBP_ID_26331226 Human_Splice_Rec_1774944,Human_Splice_Rec_1774945,Human_Splice_Rec_1775034,Human_Splice_Rec_1775035,Human_Splice_Rec_1775086,Human_Splice_Rec_1775087,Human_Splice_Rec_1775164,Human_Splice_Rec_1775165 Human_miRNA_ID_315557,Human_miRNA_ID_318829,Human_miRNA_ID_2073036,Human_miRNA_ID_2074717,Human_miRNA_ID_3064878 RMVar_hsa_circ_181956,RMVar_hsa_circ_103898,RMVar_hsa_circ_120719,RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_109586,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_92465,RMVar_hsa_circ_181958,RMVar_hsa_circ_29277,RMVar_hsa_circ_181959,RMVar_hsa_circ_181957,RMVar_hsa_circ_17186,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953 104481 RMVar_ID_104481 Human_SNP_ID_616551110 m1A Human chr17 + 7904414 7904414 7904414 CAGTGGAAGGATTAGCAAAGAAGGAGACCCCCAGTGTTCATTCATTCTGTTGCCCTTCAGATTGA CAGTGGAAGGATTAGCAAAGAAGGAGACCCCCGGTGTTCATTCATTCTGTTGCCCTTCAGATTGA A G CHD3 Ensembl:ENSG00000170004 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7904409..7904638 26863196 MeRIP-seq:(Medium) rs1343654132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181956,RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_92465,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953,RMVar_hsa_circ_109671,RMVar_hsa_circ_87683,RMVar_hsa_circ_181963,RMVar_hsa_circ_119752,RMVar_hsa_circ_181964,RMVar_hsa_circ_181965,RMVar_hsa_circ_49814,RMVar_hsa_circ_88217,RMVar_hsa_circ_181969 104482 RMVar_ID_104482 Human_SNP_ID_616551845 m1A Human chr17 + 7906955 7906955 7906955 GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGAGCCTCCTCTCCTACCAAAACGTCTCCCACCAC GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGGGCCTCCTCTCCTACCAAAACGTCTCCCACCAC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7906904..7907000 26863196 MeRIP-seq:(Medium) rs1156230891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131738,Human_RBP_ID_2524984 Human_Splice_Rec_1774978,Human_Splice_Rec_1774979,Human_Splice_Rec_1775120,Human_Splice_Rec_1775121,Human_Splice_Rec_1775198,Human_Splice_Rec_1775199,Human_Splice_Rec_1775264,Human_Splice_Rec_1775265 Human_miRNA_ID_881101,Human_miRNA_ID_1035780,Human_miRNA_ID_1395521,Human_miRNA_ID_1546930,Human_miRNA_ID_2793519 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953,RMVar_hsa_circ_109671,RMVar_hsa_circ_87683,RMVar_hsa_circ_181963,RMVar_hsa_circ_119752,RMVar_hsa_circ_181964,RMVar_hsa_circ_181965,RMVar_hsa_circ_88217,RMVar_hsa_circ_181969,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 104483 RMVar_ID_104483 Human_SNP_ID_616552046 m1A Human chr17 + 7907476 7907476 7907476 AGATGGAGCCTGAACCTGGGTACCGTGGGGACAGAGAGAAGTCAGGTGGGTGCATGGCCTTAGGA AGATGGAGCCTGAACCTGGGTACCGTGGGGACGGAGAGAAGTCAGGTGGGTGCATGGCCTTAGGA A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7907426..7907975 26863196 MeRIP-seq:(Medium) rs1401753022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8823050,Human_RBP_ID_18990446,Human_RBP_ID_26331235 Human_Splice_Rec_1774983,Human_Splice_Rec_1775125,Human_Splice_Rec_1775203,Human_Splice_Rec_1775269 Human_miRNA_ID_3118630 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_181954,RMVar_hsa_circ_181953,RMVar_hsa_circ_87683,RMVar_hsa_circ_181963,RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 104484 RMVar_ID_104484 Human_SNP_ID_616552120 m1A Human chr17 - 7907642 7907642 7907642 CTCCGGCCTCTCCCTGTGTTCCTGTCCATCCAACGGCTTCTCCTCCCCCCTTTCTCCTGGCGTCG CTCCGGCCTCTCCCTGTGTTCCTGTCCATCCAGCGGCTTCTCCTCCCCCCTTTCTCCTGGCGTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7907155..7907745 26863196 MeRIP-seq:(Medium) rs1338713537 Functional Loss SNV dbSNP153 33..33 33 - - - 104485 RMVar_ID_104485 Human_SNP_ID_616552354 m1A Human chr17 - 7908510 7908510 7908510 CTTTTCCTTCTTGCATGTGTATCAAAGGATACAGGACAATCCCAGCCAGAAGCCAATAGTCATGT CTTTTCCTTCTTGCATGTGTATCAAAGGATACCGGACAATCCCAGCCAGAAGCCAATAGTCATGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7908472..7908798 32194978 MeRIP-seq:(Medium) rs1467861490 Functional Loss SNV dbSNP153 33..33 33 - - - 104486 RMVar_ID_104486 Human_SNP_ID_616552704 m1A Human chr17 + 7909717 7909713 7909717 AATGCACCATACAGATCCCTGGCTGTGATCAAACAAATCACATTCCCTCACATGTGTTTCACCCC AATGCACCATACAGATCCCTGGCTGTGAT____CAAATCACATTCCCTCACATGTGTTTCACCCC TCAAA T CHD3 Ensembl:ENSG00000170004 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7909710..7910300 26863196 MeRIP-seq:(Medium) rs1276220241 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 104487 RMVar_ID_104487 Human_SNP_ID_616552918 m1A Human chr17 + 7910501 7910501 7910501 GACGTGACCCGCCTGCCAGCCACGCTGTCCCGAATACCCCCCATCGCAGCCCGCCTTCAGATGTC GACGTGACCCGCCTGCCAGCCACGCTGTCCCGGATACCCCCCATCGCAGCCCGCCTTCAGATGTC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr17:7910451..7910525;chr17:7909364..7910606 26863196 MeRIP-seq:(Medium) rs1303171057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1774994,Human_Splice_Rec_1774995,Human_Splice_Rec_1775136,Human_Splice_Rec_1775137,Human_Splice_Rec_1775212,Human_Splice_Rec_1775213,Human_Splice_Rec_1775280,Human_Splice_Rec_1775281,Human_Splice_Rec_1775302,Human_Splice_Rec_1775303,Human_Splice_Rec_1775314,Human_Splice_Rec_1775315,Human_Splice_Rec_1775327 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 104488 RMVar_ID_104488 Human_SNP_ID_616552932 m1A Human chr17 + 7910527 7910527 7910527 GTCCCGAATACCCCCCATCGCAGCCCGCCTTCAGATGTCCGAGCGCAGCATCCTCAGCCGGCTGG GTCCCGAATACCCCCCATCGCAGCCCGCCTTCGGATGTCCGAGCGCAGCATCCTCAGCCGGCTGG A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:7910476..7910636 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1774994,Human_Splice_Rec_1774995,Human_Splice_Rec_1775136,Human_Splice_Rec_1775137,Human_Splice_Rec_1775212,Human_Splice_Rec_1775213,Human_Splice_Rec_1775280,Human_Splice_Rec_1775281,Human_Splice_Rec_1775302,Human_Splice_Rec_1775303,Human_Splice_Rec_1775314,Human_Splice_Rec_1775315,Human_Splice_Rec_1775327 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 104489 RMVar_ID_104489 Human_SNP_ID_616553283 m1A Human chr17 + 7911548 7911548 7911548 GGCATTGGTGTCAGACGGGCTGGATCGGAAGGAGCCCCGAGCCGGGGAGGTGATCTGTATAGACG GGCATTGGTGTCAGACGGGCTGGATCGGAAGGTGCCCCGAGCCGGGGAGGTGATCTGTATAGACG A T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7910421..7912511 32194978 MeRIP-seq:(Medium) rs781361149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13186892 Human_Splice_Rec_1774998,Human_Splice_Rec_1775140,Human_Splice_Rec_1775216,Human_Splice_Rec_1775284,Human_Splice_Rec_1775306,Human_Splice_Rec_1775326,Human_Splice_Rec_1775330 Human_miRNA_ID_2016826 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965 104490 RMVar_ID_104490 Human_SNP_ID_616553363 m1A Human chr17 + 7911764 7911764 7911764 CTCTCTTCAAGAAGGGCCCTTTGTCTTTCTCCACTCCCACACACCTTTCCCACCAAGCCTTGAAG CTCTCTTCAAGAAGGGCCCTTTGTCTTTCTCCGCTCCCACACACCTTTCCCACCAAGCCTTGAAG A G CHD3 Ensembl:ENSG00000170004 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7911726..7911775 26863196 MeRIP-seq:(Medium) rs1335347942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502010,Human_RBP_ID_17902358,Human_RBP_ID_18710634,Human_RBP_ID_27458316 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181978 104491 RMVar_ID_104491 Human_SNP_ID_616553419 m1A Human chr17 + 7912045 7912045 7912045 AGAGCTTTGAAGAGAGGAGGGGGACTTTAGAGAGGGATGAAAATGAGCCCTGGGAGGGAGGAAGG AGAGCTTTGAAGAGAGGAGGGGGACTTTAGAGGGGGATGAAAATGAGCCCTGGGAGGGAGGAAGG A G CHD3 Ensembl:ENSG00000170004 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7911925..7912175 26863196 MeRIP-seq:(Medium) rs1205019155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6649866 Human_miRNA_ID_444620,Human_miRNA_ID_2956323 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965 104492 RMVar_ID_104492 Human_SNP_ID_616553420 m1A Human chr17 + 7912049 7912049 7912049 CTTTGAAGAGAGGAGGGGGACTTTAGAGAGGGATGAAAATGAGCCCTGGGAGGGAGGAAGGGACG CTTTGAAGAGAGGAGGGGGACTTTAGAGAGGGCTGAAAATGAGCCCTGGGAGGGAGGAAGGGACG A C CHD3 Ensembl:ENSG00000170004 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7912001..7912200 26863196 MeRIP-seq:(Medium) rs1482712672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_444620,Human_miRNA_ID_2956323 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965 104493 RMVar_ID_104493 Human_SNP_ID_616553443 m1A Human chr17 + 7912145 7912145 7912145 CCTCTCCCCACGTGGAGGGTGGAGCAGTTATGAGGGAGGAAGTCAACTGCTGTTCAGCCTCAGAA CCTCTCCCCACGTGGAGGGTGGAGCAGTTATGGGGGAGGAAGTCAACTGCTGTTCAGCCTCAGAA A G CHD3 Ensembl:ENSG00000170004 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7912101..7912150;chr17:7911799..7912200;chr17:7911535..7912200 26863196 MeRIP-seq:(Medium) rs1255806899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21976049,Human_RBP_ID_26457108,Human_RBP_ID_26973395 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965 104494 RMVar_ID_104494 Human_SNP_ID_616554437 m1A Human chr17 - 7915794 7915794 7915794 AGCAGCGACGCTGACGGAGAGGCGGAGGAAGAAGGGGAGAGCGAGAAGGGGGCGGGGCCTAGGAG AGCAGCGACGCTGACGGAGAGGCGGAGGAAGAGGGGGAGAGCGAGAAGGGGGCGGGGCCTAGGAG T C RNF227 Ensembl:ENSG00000179859 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7915574..7915932 26863196 MeRIP-seq:(Medium) rs1263706392 Functional Loss SNV dbSNP153 33..33 33 - - - 104495 RMVar_ID_104495 Human_SNP_ID_616558694 m1A Human chr17 - 7930495 7930495 7930495 TGTAAGCCCCCGCACCCCCACCCCCTGCCCAGAGCAACAGCCTAAAGGCCTGCCCTGATGCTCTC TGTAAGCCCCCGCACCCCCACCCCCTGCCCAGGGCAACAGCCTAAAGGCCTGCCCTGATGCTCTC T C AC104581.2,TRAPPC1 Ensembl:ENSG00000262730,Ensembl:ENSG00000170043 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7930376..7930725 26863196 MeRIP-seq:(Medium) rs1360998263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236699,Human_RBP_ID_502097,Human_RBP_ID_17378176,Human_RBP_ID_17654577,Human_RBP_ID_18941371,Human_RBP_ID_26813162 Human_miRNA_ID_935403,Human_miRNA_ID_955347,Human_miRNA_ID_1966458,Human_miRNA_ID_2361915,Human_miRNA_ID_2425241,Human_miRNA_ID_2434903,Human_miRNA_ID_2908353,Human_miRNA_ID_3027192 RMVar_hsa_circ_95197,RMVar_hsa_circ_181981,RMVar_hsa_circ_78714,RMVar_hsa_circ_181980 104496 RMVar_ID_104496 Human_SNP_ID_616558705 m1A Human chr17 - 7930514 7930514 7930514 GCCAACTAAGGGCCCCCACTGTAAGCCCCCGCACCCCCACCCCCTGCCCAGAGCAACAGCCTAAA GCCAACTAAGGGCCCCCACTGTAAGCCCCCGCCCCCCCACCCCCTGCCCAGAGCAACAGCCTAAA T G AC104581.2,TRAPPC1 Ensembl:ENSG00000262730,Ensembl:ENSG00000170043 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:7930414..7930644 26863196 MeRIP-seq:(Medium) rs1421243913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502102,Human_RBP_ID_17262681,Human_RBP_ID_17378176,Human_RBP_ID_17654577,Human_RBP_ID_18941371,Human_RBP_ID_26813162 Human_miRNA_ID_2434903 RMVar_hsa_circ_95197,RMVar_hsa_circ_181981,RMVar_hsa_circ_78714,RMVar_hsa_circ_181980 104497 RMVar_ID_104497 Human_SNP_ID_616558715 m1A Human chr17 - 7930529 7930529 7930529 CCCTTCCGAACCTGTGCCAACTAAGGGCCCCCACTGTAAGCCCCCGCACCCCCACCCCCTGCCCA CCCTTCCGAACCTGTGCCAACTAAGGGCCCCCGCTGTAAGCCCCCGCACCCCCACCCCCTGCCCA T C AC104581.2,TRAPPC1 Ensembl:ENSG00000262730,Ensembl:ENSG00000170043 Protein coding,Protein coding 3'UTR,3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7930431..7930603 26863410 MeRIP-seq:(Medium) rs1470629806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502104,Human_RBP_ID_1010993,Human_RBP_ID_4457209,Human_RBP_ID_5114541,Human_RBP_ID_9076848,Human_RBP_ID_17262681,Human_RBP_ID_17378176,Human_RBP_ID_17654094,Human_RBP_ID_17902407,Human_RBP_ID_18439819,Human_RBP_ID_18941371,Human_RBP_ID_23753314,Human_RBP_ID_26811927 Human_Splice_Rec_1775411 Human_miRNA_ID_1418795,Human_miRNA_ID_1418796,Human_miRNA_ID_1802320,Human_miRNA_ID_1802321 RMVar_hsa_circ_95197,RMVar_hsa_circ_181981,RMVar_hsa_circ_78714,RMVar_hsa_circ_181980 104498 RMVar_ID_104498 Human_SNP_ID_616558716 m1A Human chr17 - 7930529 7930529 7930529 CCCTTCCGAACCTGTGCCAACTAAGGGCCCCCACTGTAAGCCCCCGCACCCCCACCCCCTGCCCA CCCTTCCGAACCTGTGCCAACTAAGGGCCCCCCCTGTAAGCCCCCGCACCCCCACCCCCTGCCCA T G AC104581.2,TRAPPC1 Ensembl:ENSG00000262730,Ensembl:ENSG00000170043 Protein coding,Protein coding 3'UTR,3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:7930431..7930603 26863410 MeRIP-seq:(Medium) rs1470629806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502104,Human_RBP_ID_1010993,Human_RBP_ID_4457209,Human_RBP_ID_5114541,Human_RBP_ID_9076848,Human_RBP_ID_17262681,Human_RBP_ID_17378176,Human_RBP_ID_17654094,Human_RBP_ID_17902407,Human_RBP_ID_18439819,Human_RBP_ID_18941371,Human_RBP_ID_23753314,Human_RBP_ID_26811927 Human_Splice_Rec_1775411 Human_miRNA_ID_1418795,Human_miRNA_ID_1418796,Human_miRNA_ID_1802320,Human_miRNA_ID_1802321 RMVar_hsa_circ_95197,RMVar_hsa_circ_181981,RMVar_hsa_circ_78714,RMVar_hsa_circ_181980 104499 RMVar_ID_104499 Human_SNP_ID_616558744 m1A Human chr17 - 7930602 7930602 7930602 TGCCCTTCTTCTCCGCCCGGGCTGGCTGAAGCAACCTACCTCAAGTCTCAGGAGAATTCATGTCT TGCCCTTCTTCTCCGCCCGGGCTGGCTGAAGCGACCTACCTCAAGTCTCAGGAGAATTCATGTCT T C AC104581.2,TRAPPC1 Ensembl:ENSG00000262730,Ensembl:ENSG00000170043 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7930551..7930667 26863196 MeRIP-seq:(Medium) rs754740429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502104,Human_RBP_ID_766066,Human_RBP_ID_822250,Human_RBP_ID_1870416,Human_RBP_ID_4457212,Human_RBP_ID_5143098,Human_RBP_ID_5184685,Human_RBP_ID_8465273,Human_RBP_ID_9076850,Human_RBP_ID_9326475,Human_RBP_ID_13187678,Human_RBP_ID_17262286,Human_RBP_ID_17378178,Human_RBP_ID_17654094,Human_RBP_ID_18942858,Human_RBP_ID_23753316,Human_RBP_ID_26973593,Human_RBP_ID_27261364 Human_Splice_Rec_1775411 Human_miRNA_ID_1914950,Human_miRNA_ID_1917399,Human_miRNA_ID_1919851,Human_miRNA_ID_1922310,Human_miRNA_ID_1924764,Human_miRNA_ID_1927215,Human_miRNA_ID_1929664,Human_miRNA_ID_1932116,Human_miRNA_ID_2629941,Human_miRNA_ID_2643055,Human_miRNA_ID_3125800 RMVar_hsa_circ_95197,RMVar_hsa_circ_181981,RMVar_hsa_circ_78714,RMVar_hsa_circ_181980 104500 RMVar_ID_104500 Human_SNP_ID_616559138 m1A Human chr17 - 7931826 7931826 7931826 GAGCGAGGCTCACACTCCCTGCCCTGCAGATGACTGTCCACAACCTGTACCTGTTTGACCGGAAT GAGCGAGGCTCACACTCCCTGCCCTGCAGATGGCTGTCCACAACCTGTACCTGTTTGACCGGAAT T C TRAPPC1 Ensembl:ENSG00000170043 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7931778..7931950 26863196 MeRIP-seq:(Medium) rs1214082703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502129,Human_RBP_ID_1544086,Human_RBP_ID_1870433,Human_RBP_ID_3538947,Human_RBP_ID_4457264,Human_RBP_ID_5497978,Human_RBP_ID_8465291,Human_RBP_ID_9375316,Human_RBP_ID_13187806,Human_RBP_ID_18710788,Human_RBP_ID_23753336 Human_Splice_Rec_1775422,Human_Splice_Rec_1775423,Human_Splice_Rec_1775430,Human_Splice_Rec_1775431,Human_Splice_Rec_1775435,Human_Splice_Rec_1775441,Human_Splice_Rec_1775446,Human_Splice_Rec_1775447,Human_Splice_Rec_1775452,Human_Splice_Rec_1775453,Human_Splice_Rec_1775457 104501 RMVar_ID_104501 Human_SNP_ID_616559161 m1A Human chr17 - 7931877 7931877 7931877 TGGAAGGCTGTGGGTCCGGGAACCCGAGCCCAAGGAGTGGGGGCGGCCCCGGAGCGAGGCTCACA TGGAAGGCTGTGGGTCCGGGAACCCGAGCCCAGGGAGTGGGGGCGGCCCCGGAGCGAGGCTCACA T C TRAPPC1 Ensembl:ENSG00000170043 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7931781..7931925 32194978 MeRIP-seq:(Medium) rs749279689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502133,Human_RBP_ID_767370,Human_RBP_ID_4457266,Human_RBP_ID_23753337 104502 RMVar_ID_104502 Human_SNP_ID_616559309 m1A Human chr17 + 7932262 7932262 7932262 GTTTTGAGCGTAGGGGGAGGCGTGAGAGGGGGATCTCAGGGGAGGAGGTCAATCGCTTGCCCCCC GTTTTGAGCGTAGGGGGAGGCGTGAGAGGGGGGTCTCAGGGGAGGAGGTCAATCGCTTGCCCCCC A G CNTROB Ensembl:ENSG00000170037 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7932211..7932450 26863196 MeRIP-seq:(Medium) rs1206692577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5143099,Human_RBP_ID_9353299,Human_RBP_ID_9422766,Human_RBP_ID_18419872 104503 RMVar_ID_104503 Human_SNP_ID_616559397 m1A Human chr17 - 7932665 7932665 7932665 TTCTCACACCCAAAACGTCCCAACGGAAACGGACCCAAATCCACTAGGAGCCCAATTTCTGTCCC TTCTCACACCCAAAACGTCCCAACGGAAACGGGCCCAAATCCACTAGGAGCCCAATTTCTGTCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7932565..7932666 32194978 MeRIP-seq:(Medium) rs1188981759 Functional Loss SNV dbSNP153 33..33 33 - - - 104504 RMVar_ID_104504 Human_SNP_ID_616559428 m1A Human chr17 - 7932813 7932813 7932813 CGTTAAGAGGGTGCAGCGCAGAGCGGGTGCGGACAGAAGACCTACTGTGGGACAACAGCGCTGCT CGTTAAGAGGGTGCAGCGCAGAGCGGGTGCGGTCAGAAGACCTACTGTGGGACAACAGCGCTGCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7932764..7932865 32194978 MeRIP-seq:(Medium) rs536056390 Functional Loss SNV dbSNP153 33..33 33 - - - 104505 RMVar_ID_104505 Human_SNP_ID_616559429 m1A Human chr17 - 7932813 7932813 7932813 CGTTAAGAGGGTGCAGCGCAGAGCGGGTGCGGACAGAAGACCTACTGTGGGACAACAGCGCTGCT CGTTAAGAGGGTGCAGCGCAGAGCGGGTGCGGGCAGAAGACCTACTGTGGGACAACAGCGCTGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7932764..7932865 32194978 MeRIP-seq:(Medium) rs536056390 Functional Loss SNV dbSNP153 33..33 33 - - - 104506 RMVar_ID_104506 Human_SNP_ID_616559920 m1A Human chr17 - 7934543 7934543 7934543 AAGCTAGGAGAACCACAAGGAGAACTCACTTGAGCAAGGTGGCTGTGCTATCACTGTCAAAGGAG AAGCTAGGAGAACCACAAGGAGAACTCACTTGGGCAAGGTGGCTGTGCTATCACTGTCAAAGGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7934492..7935695 26863196 MeRIP-seq:(Medium) rs149438589 Functional Loss SNV dbSNP153 33..33 33 - - - 104507 RMVar_ID_104507 Human_SNP_ID_616560685 m1A Human chr17 + 7937251 7937250 7937252 AGCAGGAAAGTGCCAGACTGCAGCAACGGGAAAGAGAGACACTGGTGAGAAGATTGGACTGGGTT AGCAGGAAAGTGCCAGACTGCAGCAACGGGAA__AGAGACACTGGTGAGAAGATTGGACTGGGTT AAG A CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7937151..7937310 26863196 MeRIP-seq:(Medium) rs748964217 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3950097,Human_RBP_ID_13188396,Human_RBP_ID_18990451,Human_RBP_ID_27812256 Human_Splice_Rec_1775478,Human_Splice_Rec_1775479,Human_Splice_Rec_1775514,Human_Splice_Rec_1775515,Human_Splice_Rec_1775556,Human_Splice_Rec_1775568,Human_Splice_Rec_1775569,Human_Splice_Rec_1775604,Human_Splice_Rec_1775605,Human_Splice_Rec_1775614,Human_Splice_Rec_1775615,Human_Splice_Rec_1775635,Human_Splice_Rec_1775647 RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_347345,RMVar_hsa_circ_63051,RMVar_hsa_circ_323910,RMVar_hsa_circ_332345,RMVar_hsa_circ_19764 104508 RMVar_ID_104508 Human_SNP_ID_616560687 m1A Human chr17 + 7937251 7937251 7937251 AGCAGGAAAGTGCCAGACTGCAGCAACGGGAAAGAGAGACACTGGTGAGAAGATTGGACTGGGTT AGCAGGAAAGTGCCAGACTGCAGCAACGGGAAGGAGAGACACTGGTGAGAAGATTGGACTGGGTT A G CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7937151..7937310 26863196 MeRIP-seq:(Medium) rs535845365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3950097,Human_RBP_ID_13188396,Human_RBP_ID_18990451,Human_RBP_ID_27812256 Human_Splice_Rec_1775478,Human_Splice_Rec_1775479,Human_Splice_Rec_1775514,Human_Splice_Rec_1775515,Human_Splice_Rec_1775556,Human_Splice_Rec_1775568,Human_Splice_Rec_1775569,Human_Splice_Rec_1775604,Human_Splice_Rec_1775605,Human_Splice_Rec_1775614,Human_Splice_Rec_1775615,Human_Splice_Rec_1775635,Human_Splice_Rec_1775647 RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_347345,RMVar_hsa_circ_63051,RMVar_hsa_circ_323910,RMVar_hsa_circ_332345,RMVar_hsa_circ_19764 104509 RMVar_ID_104509 Human_SNP_ID_616561208 m1A Human chr17 - 7939482 7939482 7939482 TCCTACAGCCGCAGAAGAAAACCAAGCTCCTTAGTAGGCTCTTCAGAGACCAGCGATCTGCCCTC TCCTACAGCCGCAGAAGAAAACCAAGCTCCTTGGTAGGCTCTTCAGAGACCAGCGATCTGCCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7939479..7939775 26863196 MeRIP-seq:(Medium) rs1483243747 Functional Loss SNV dbSNP153 33..33 33 - - - 104510 RMVar_ID_104510 Human_SNP_ID_616562347 m1A Human chr17 + 7943518 7943518 7943518 CAGCCTACGGCAAGCAGCCTCCCTCAGGGAACATCACAGGTACGTGGGACTCACTGGGTGTCACT CAGCCTACGGCAAGCAGCCTCCCTCAGGGAACTTCACAGGTACGTGGGACTCACTGGGTGTCACT A T CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78236778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5361584,Human_RBP_ID_19078345 Human_Splice_Rec_1775485,Human_Splice_Rec_1775521,Human_Splice_Rec_1775575,Human_Splice_Rec_1775621,Human_Splice_Rec_1775641,Human_Splice_Rec_1775657 Clinvar_Rec_666,Clinvar_Rec_667 GWAS_ID_13694 RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_19764,RMVar_hsa_circ_356758,RMVar_hsa_circ_181985,RMVar_hsa_circ_344070 104511 RMVar_ID_104511 Human_SNP_ID_616562519 m1A Human chr17 + 7944221 7944221 7944221 GGTGGAAATGGCAGAACGAGAGGAACGGCAACAGCAGGTGGCTGAGGACTACGAGCTCAGGTCCT GGTGGAAATGGCAGAACGAGAGGAACGGCAACGGCAGGTGGCTGAGGACTACGAGCTCAGGTCCT A G CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7944170..7944271 32194978 MeRIP-seq:(Medium) rs770889901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236696,Human_RBP_ID_899366,Human_RBP_ID_3950099 Human_Splice_Rec_1775486,Human_Splice_Rec_1775487,Human_Splice_Rec_1775522,Human_Splice_Rec_1775523,Human_Splice_Rec_1775576,Human_Splice_Rec_1775577,Human_Splice_Rec_1775622,Human_Splice_Rec_1775623,Human_Splice_Rec_1775642,Human_Splice_Rec_1775658,Human_Splice_Rec_1775659 RMVar_hsa_circ_9763,RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_54922,RMVar_hsa_circ_356758,RMVar_hsa_circ_181985,RMVar_hsa_circ_344070,RMVar_hsa_circ_86347,RMVar_hsa_circ_181986 104512 RMVar_ID_104512 Human_SNP_ID_616562560 m1A Human chr17 + 7944322 7944322 7944322 TCCCATGGGTAGAGCCCAAACTGGGAACGGTGAAGAGCTGCTCCCTTGATTGATCTGTCCTCCTC TCCCATGGGTAGAGCCCAAACTGGGAACGGTGTAGAGCTGCTCCCTTGATTGATCTGTCCTCCTC A T CNTROB Ensembl:ENSG00000170037 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7944320..7944408 26863196 MeRIP-seq:(Medium) rs771949369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820607,Human_RBP_ID_5361585,Human_RBP_ID_19078347,Human_RBP_ID_23257124 RMVar_hsa_circ_9763,RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_54922,RMVar_hsa_circ_356758,RMVar_hsa_circ_181985,RMVar_hsa_circ_344070,RMVar_hsa_circ_86347,RMVar_hsa_circ_181986 104513 RMVar_ID_104513 Human_SNP_ID_616563715 m1A Human chr17 - 7948621 7948621 7948621 GGAGAATCCTTCCTCCTTCCTCCCAGGCTTGTACCCGCTGTGTTCCAGCCTCTTCAGGTAGAGCA GGAGAATCCTTCCTCCTTCCTCCCAGGCTTGTGCCCGCTGTGTTCCAGCCTCTTCAGGTAGAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7948571..7948721 32194978 MeRIP-seq:(Medium) rs762531451 Functional Loss SNV dbSNP153 33..33 33 - - - 104514 RMVar_ID_104514 Human_SNP_ID_616563939 m1A Human chr17 + 7949435 7949435 7949435 CCTCGCCGCCTTGCTACAGCCCCCAAGACTGAAAAACCTCCCGCACGGAAGAAAAGTGGGCACCC CCTCGCCGCCTTGCTACAGCCCCCAAGACTGATAAACCTCCCGCACGGAAGAAAAGTGGGCACCC A T CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7949332..7949519 26863196 MeRIP-seq:(Medium) rs751040454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25336678 Human_Splice_Rec_1775502,Human_Splice_Rec_1775538,Human_Splice_Rec_1775592,Human_Splice_Rec_1775672,Human_Splice_Rec_1775684 RMVar_hsa_circ_118158,RMVar_hsa_circ_181990 104515 RMVar_ID_104515 Human_SNP_ID_616594309 m1A Human chr17 + 8064453 8064453 8064453 AGCACCGGCTCTGACAAGAGGATTAGGTGGGGAAGTTGAGTGGTGGATCAGTGAGTGGAAGAGGG AGCACCGGCTCTGACAAGAGGATTAGGTGGGGGAGTTGAGTGGTGGATCAGTGAGTGGAAGAGGG A G AC129492.6 Ensembl:ENSG00000275011 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8064402..8064783 26863196 MeRIP-seq:(Medium) rs1201275843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3545066,Human_RBP_ID_5186995,Human_RBP_ID_9422228,Human_RBP_ID_18460142,Human_RBP_ID_22357157,Human_RBP_ID_22415897 104516 RMVar_ID_104516 Human_SNP_ID_616594766 m1A Human chr17 + 8066203 8066203 8066203 CGCACCACTGCACTCCAGCCTGGGCGACAGAGAGAGACTATAGAAAGAAAGGAAGAAAGAAAGGA CGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTATAGAAAGAAAGGAAGAAAGAAAGGA A C AC129492.6 Ensembl:ENSG00000275011 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8066171..8066267 26863196 MeRIP-seq:(Medium) rs1392569672 Functional Loss SNV dbSNP153 33..33 33 - - - 104517 RMVar_ID_104517 Human_SNP_ID_616598472 m1A Human chr17 - 8079674 8079674 8079674 CTCTCCCCACCTCCGGCGCCCGCGCCAGTCCCAGGCAAGCCCGCACCCCGCGTCCCTGTCCCCGT CTCTCCCCACCTCCGGCGCCCGCGCCAGTCCCGGGCAAGCCCGCACCCCGCGTCCCTGTCCCCGT T C ALOX12B Ensembl:ENSG00000179477 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8079651..8079835 26863196 MeRIP-seq:(Medium) rs1261731452 Functional Loss SNV dbSNP153 33..33 33 - - - 104518 RMVar_ID_104518 Human_SNP_ID_616610910 m1A Human chr17 + 8119211 8119211 8119211 CATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCGGGCGGCATGTCTTTGCTTTT CATCAGACTTTTAATCTGAGGGTCCAGGGTTCGAGTCCCTGTTCGGGCGGCATGTCTTTGCTTTT A G TRK1,TRK-TTT3-1,TRK-TTT3-5,tRNA-Lys-TTT-3-1 RNACentral:URS00002222F7,RNACentral:URS000032F6AC,RNACentral:URS00008FED2A,RNACentral:URS000022DD4A tRNA,tRNA,tRNA,tRNA intron,intron,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs947357932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269879,Human_RBP_ID_1185257,Human_RBP_ID_1370323,Human_RBP_ID_1545787,Human_RBP_ID_1871403,Human_RBP_ID_3540153,Human_RBP_ID_4481453,Human_RBP_ID_5184740,Human_RBP_ID_5260454,Human_RBP_ID_5275146,Human_RBP_ID_5420639,Human_RBP_ID_5498082,Human_RBP_ID_5582817,Human_RBP_ID_6653309,Human_RBP_ID_8253869,Human_RBP_ID_8466897,Human_RBP_ID_8823916,Human_RBP_ID_13204585,Human_RBP_ID_17007171,Human_RBP_ID_17693403,Human_RBP_ID_17906565,Human_RBP_ID_18439930,Human_RBP_ID_18712502,Human_RBP_ID_19031161,Human_RBP_ID_20283666,Human_RBP_ID_22224713,Human_RBP_ID_22422022,Human_RBP_ID_22807608,Human_RBP_ID_22958678,Human_RBP_ID_23129904,Human_RBP_ID_23172517,Human_RBP_ID_23276359,Human_RBP_ID_23308945,Human_RBP_ID_24416242,Human_RBP_ID_24481655,Human_RBP_ID_26456756,Human_RBP_ID_26976161,Human_RBP_ID_27157127,Human_RBP_ID_27263200,Human_RBP_ID_27459458 104519 RMVar_ID_104519 Human_SNP_ID_616611564 m1A Human chr17 - 8120329 8120329 8120329 TAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGAATCCCACCGCTGCCAGGCTGGAGTTTTTCTGG TAGGCTCCAGTCTCTTCGGAGGCGTGGGTTCGCATCCCACCGCTGCCAGGCTGGAGTTTTTCTGG T G tRNA-Leu-TAG-1-1 RNACentral:URS00001B506A tRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs921724769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503564,Human_RBP_ID_1185263,Human_RBP_ID_1545844,Human_RBP_ID_3540163,Human_RBP_ID_4481472,Human_RBP_ID_5275153,Human_RBP_ID_5420641,Human_RBP_ID_5442080,Human_RBP_ID_5467231,Human_RBP_ID_5498084,Human_RBP_ID_5582820,Human_RBP_ID_6653419,Human_RBP_ID_8253870,Human_RBP_ID_8466929,Human_RBP_ID_9077129,Human_RBP_ID_9888221,Human_RBP_ID_18712526,Human_RBP_ID_20283720,Human_RBP_ID_22060666,Human_RBP_ID_22224741,Human_RBP_ID_22500849,Human_RBP_ID_22807623,Human_RBP_ID_22961887,Human_RBP_ID_23110439,Human_RBP_ID_23129916,Human_RBP_ID_23756000,Human_RBP_ID_24417661,Human_RBP_ID_24482146,Human_RBP_ID_26456758,Human_RBP_ID_26976187,Human_RBP_ID_27157012,Human_RBP_ID_27263203,Human_RBP_ID_27459460 104520 RMVar_ID_104520 Human_SNP_ID_616612056 m1A Human chr17 - 8121121 8121121 8121121 AGACAGGTAAGTAAAGAAGAGAGCAGAGCGGGAACTGAGATCGAAATTGAAACCAGGTGGAAAGA AGACAGGTAAGTAAAGAAGAGAGCAGAGCGGGCACTGAGATCGAAATTGAAACCAGGTGGAAAGA T G HES7 Ensembl:ENSG00000179111 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8121071..8121136 26863196 MeRIP-seq:(Medium) rs945168238 Functional Loss SNV dbSNP153 33..33 33 - - - 104521 RMVar_ID_104521 Human_SNP_ID_616612583 m1A Human chr17 - 8122404 8122404 8122404 CTGTAGAACCTCCGGAACCCGAAGCTGGAGAAAGCGGAGATATTGGAGTTCGCCGTGGGCTACTT CTGTAGAACCTCCGGAACCCGAAGCTGGAGAAGGCGGAGATATTGGAGTTCGCCGTGGGCTACTT T C HES7 Ensembl:ENSG00000179111 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:8122326..8124169;chr17:8121612..8124100;chr17:8122340..8124092 26863196 MeRIP-seq:(Medium) rs1257930276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1776016,Human_Splice_Rec_1776017,Human_Splice_Rec_1776022,Human_Splice_Rec_1776023,Human_Splice_Rec_1776028,Human_Splice_Rec_1776029 104522 RMVar_ID_104522 Human_SNP_ID_616613496 m1A Human chr17 - 8125627 8125627 8125627 TGGTCCCGAATGGTTGCCGTGGGTGGAGCGCCAAGTCATCCTTCCTCTCGTCCGGATCCGGCCAC TGGTCCCGAATGGTTGCCGTGGGTGGAGCGCCGAGTCATCCTTCCTCTCGTCCGGATCCGGCCAC T C lnc-HES7-1 RNACentral:URS00008B754C lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8125533..8125743 26863196 MeRIP-seq:(Medium) rs528351779 Functional Loss SNV dbSNP153 33..33 33 - - - 104523 RMVar_ID_104523 Human_SNP_ID_616613665 m1A Human chr17 + 8125801 8125801 8125801 TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGATTCCCGGCCAATGCACGAGTACAGTTTTCTTT TTCTCGCCTGCCACGCGGGAGGCCCGGGTTCGGTTCCCGGCCAATGCACGAGTACAGTTTTCTTT A G lnc-HES7-1 RNACentral:URS00008B754C lincRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 29072297,31548705,31548705 m1A-MAP&m1A-IP-seq&m1A-quant-seq:(High) rs938196016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23756018 104524 RMVar_ID_104524 Human_SNP_ID_616613846 m1A Human chr17 - 8126368 8126368 8126368 AGATGCAGACGCCAAGACGCGGAGAGACGCGGAATCAGAGATGCGGAGGGAGGAGACCACCAACA AGATGCAGACGCCAAGACGCGGAGAGACGCGGCATCAGAGATGCGGAGGGAGGAGACCACCAACA T G lnc-HES7-1 RNACentral:URS00008B754C lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8125955..8126552 26863196 MeRIP-seq:(Medium) rs898969848 Functional Loss SNV dbSNP153 33..33 33 - - - 104525 RMVar_ID_104525 Human_SNP_ID_616617703 m1A Human chr17 - 8139467 8139452 8139467 GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTGAGTTAGCGGGGAGTGA GCCTGTCTAGTAAACAGGAGATCCTGGGTTCG_______________TGAGTTAGCGGGGAGTGA AGGCACCGCTGGGATT A tRNA-Thr-AGT-5-1 RNACentral:URS000023FFA7 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1351514071 Functional Loss DEL dbSNP153 33..47 33 - - - Human_RBP_ID_503649,Human_RBP_ID_1545911,Human_RBP_ID_8466995,Human_RBP_ID_9888225,Human_RBP_ID_20284000,Human_RBP_ID_22224851,Human_RBP_ID_23129943,Human_RBP_ID_26976335 104526 RMVar_ID_104526 Human_SNP_ID_616617717 m1A Human chr17 - 8139467 8139467 8139467 GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTGAGTTAGCGGGGAGTGA GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGGATCCCAGCGGTGCCTGAGTTAGCGGGGAGTGA T C tRNA-Thr-AGT-5-1 RNACentral:URS000023FFA7 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1242434443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503649,Human_RBP_ID_1545911,Human_RBP_ID_8466995,Human_RBP_ID_9888225,Human_RBP_ID_20284000,Human_RBP_ID_22224851,Human_RBP_ID_23129943,Human_RBP_ID_26976335 104527 RMVar_ID_104527 Human_SNP_ID_616618280 m1A Human chr17 - 8141166 8141166 8141166 GAGAGGGCTGCGAGGAGGCCCAAGGCGGGGCCAAGGCTTCAAGCTCTCAGGACTTGGCTATGGAG GAGAGGGCTGCGAGGAGGCCCAAGGCGGGGCCGAGGCTTCAAGCTCTCAGGACTTGGCTATGGAG T C PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8141116..8141289 26863196 MeRIP-seq:(Medium) rs1398364032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17904683 104528 RMVar_ID_104528 Human_SNP_ID_616619336 m1A Human chr17 - 8143725 8143725 8143725 CCCGTGCCACCCTCCACCCCCTGGCCCACCCCACCAGCCACTACCCCCTTCCCAGCGGTTGTCCA CCCGTGCCACCCTCCACCCCCTGGCCCACCCCCCCAGCCACTACCCCCTTCCCAGCGGTTGTCCA T G PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8143450..8143900 26863196 MeRIP-seq:(Medium) rs950293870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503681,Human_RBP_ID_17079478,Human_RBP_ID_18941375 Human_miRNA_ID_272065,Human_miRNA_ID_1418797 104529 RMVar_ID_104529 Human_SNP_ID_616619389 m1A Human chr17 - 8143804 8143804 8143804 CTGCCGATCCAAAGCCAAGCGCTCACGCCACCACCAGAACCCTCGGGCTGAAGCGCCCTGCTATG CTGCCGATCCAAAGCCAAGCGCTCACGCCACCTCCAGAACCCTCGGGCTGAAGCGCCCTGCTATG T A PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:8143704..8143841 26863410 MeRIP-seq:(Medium) rs769887493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1776066,Human_Splice_Rec_1776170,Human_Splice_Rec_1776172 104530 RMVar_ID_104530 Human_SNP_ID_616619796 m1A Human chr17 - 8144826 8144826 8144826 TGCACACACAGAAGGAAGAGCAAGCCTTCCTCAGCCGCTTCCGAGACCTGGGCAGGCTGCGTGGA TGCACACACAGAAGGAAGAGCAAGCCTTCCTCTGCCGCTTCCGAGACCTGGGCAGGCTGCGTGGA T A PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8144775..8145025 32194978 MeRIP-seq:(Medium) rs3027190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1776065,Human_Splice_Rec_1776149,Human_Splice_Rec_1776168,Human_Splice_Rec_1776169,Human_Splice_Rec_1776171,Human_Splice_Rec_1776209 RMVar_hsa_circ_72441 104531 RMVar_ID_104531 Human_SNP_ID_616621416 m1A Human chr17 - 8148662 8148662 8148662 CACAGCCGTGCTGCCTGCTGATTGCAGAGCGCATCCATTCGGGTTACGAAGGTGGGCAGGTCAGG CACAGCCGTGCTGCCTGCTGATTGCAGAGCGCGTCCATTCGGGTTACGAAGGTGGGCAGGTCAGG T C PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8148056..8148725 32194978 MeRIP-seq:(Medium) rs769554705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1776045,Human_Splice_Rec_1776087,Human_Splice_Rec_1776129,Human_Splice_Rec_1776187,Human_Splice_Rec_1776225,Human_Splice_Rec_1776251 104532 RMVar_ID_104532 Human_SNP_ID_616622394 m1A Human chr17 - 8150664 8150664 8150664 CCCTAGAAGGGGCTGATGGGGGAGGGGACCCCAGGCCTGGGGAATCATTTTGTCCTGGGGGCGTC CCCTAGAAGGGGCTGATGGGGGAGGGGACCCCCGGCCTGGGGAATCATTTTGTCCTGGGGGCGTC T G PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:8150615..8150796 26863196 MeRIP-seq:(Medium) rs774716516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9377513,Human_RBP_ID_22442808,Human_RBP_ID_26976435 104533 RMVar_ID_104533 Human_SNP_ID_616625121 m1A Human chr17 - 8160090 8160090 8160090 CGCAGGTGGTGGGGAGCCTGGGCTTTTGGGGAACCAGGCTGCTCTGGTCCCCAGCATTGCCTCCT CGCAGGTGGTGGGGAGCCTGGGCTTTTGGGGAGCCAGGCTGCTCTGGTCCCCAGCATTGCCTCCT T C AC129492.3,VAMP2 Ensembl:ENSG00000263620,Ensembl:ENSG00000220205 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8160039..8160139 32194978 MeRIP-seq:(Medium) rs1332413575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_503912,Human_RBP_ID_6654133,Human_RBP_ID_8467252,Human_RBP_ID_13209602,Human_RBP_ID_20285032,Human_RBP_ID_23756705 104534 RMVar_ID_104534 Human_SNP_ID_616625347 m1A Human chr17 + 8160544 8160544 8160544 GAGAGGGACTATTGCATAGCAGATGCAAATGAAGGGACTTGGGGCTAGTCAGGAAGAAAGGGAAA GAGAGGGACTATTGCATAGCAGATGCAAATGACGGGACTTGGGGCTAGTCAGGAAGAAAGGGAAA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8160495..8160584 26863196 MeRIP-seq:(Medium) rs1318417634 Functional Loss SNV dbSNP153 33..33 33 - - - 104535 RMVar_ID_104535 Human_SNP_ID_616625462 m1A Human chr17 - 8160830 8160830 8160830 GCACTTAAATCCCCGAGGAGTCTGCCCTGCCTAGAGAAGGGCCTCTCCCCCAACCCTCAGCCGTT GCACTTAAATCCCCGAGGAGTCTGCCCTGCCTGGAGAAGGGCCTCTCCCCCAACCCTCAGCCGTT T C AC129492.3,VAMP2 Ensembl:ENSG00000263620,Ensembl:ENSG00000220205 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8160781..8161178 32194978 MeRIP-seq:(Medium) rs748294427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238343,Human_RBP_ID_503935,Human_RBP_ID_767650,Human_RBP_ID_1289765,Human_RBP_ID_18712862,Human_RBP_ID_20285054,Human_RBP_ID_23756734,Human_RBP_ID_25333126 Human_Splice_Rec_1776300,Human_Splice_Rec_1776314 Human_miRNA_ID_112454,Human_miRNA_ID_1302413,Human_miRNA_ID_1321652,Human_miRNA_ID_1478240 104536 RMVar_ID_104536 Human_SNP_ID_616625463 m1A Human chr17 - 8160830 8160830 8160830 GCACTTAAATCCCCGAGGAGTCTGCCCTGCCTAGAGAAGGGCCTCTCCCCCAACCCTCAGCCGTT GCACTTAAATCCCCGAGGAGTCTGCCCTGCCTCGAGAAGGGCCTCTCCCCCAACCCTCAGCCGTT T G AC129492.3,VAMP2 Ensembl:ENSG00000263620,Ensembl:ENSG00000220205 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8160781..8161178 32194978 MeRIP-seq:(Medium) rs748294427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238343,Human_RBP_ID_503935,Human_RBP_ID_767650,Human_RBP_ID_1289765,Human_RBP_ID_18712862,Human_RBP_ID_20285054,Human_RBP_ID_23756734,Human_RBP_ID_25333126 Human_Splice_Rec_1776300,Human_Splice_Rec_1776314 Human_miRNA_ID_112454,Human_miRNA_ID_1302413,Human_miRNA_ID_1321652,Human_miRNA_ID_1478240 104537 RMVar_ID_104537 Human_SNP_ID_616625942 m1A Human chr17 + 8162366 8162366 8162366 GGGGCAGCAGGGGGGGCCGTGGCAGCGGTAGCAGACCTGAGGAGCAGGGACGGATTAAGACCCAG GGGGCAGCAGGGGGGGCCGTGGCAGCGGTAGCGGACCTGAGGAGCAGGGACGGATTAAGACCCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:8162251..8162975 26863410 MeRIP-seq:(Medium) rs772474909 Functional Loss SNV dbSNP153 33..33 33 - - - 104538 RMVar_ID_104538 Human_SNP_ID_616626155 m1A Human chr17 - 8162919 8162919 8162919 GCCAGTCGGAGCCAGCGCGAGCCGCCGCCGCCATCACTGCCGCTGCCAAGTCCTCCACCCGCTGC GCCAGTCGGAGCCAGCGCGAGCCGCCGCCGCCGTCACTGCCGCTGCCAAGTCCTCCACCCGCTGC T C AC129492.3,VAMP2 Ensembl:ENSG00000263620,Ensembl:ENSG00000220205 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8162776..8162975 26863196 MeRIP-seq:(Medium) rs1374743853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238347,Human_RBP_ID_503944,Human_RBP_ID_767652,Human_RBP_ID_4462580 Human_Splice_Rec_1776285,Human_Splice_Rec_1776293,Human_Splice_Rec_1776315 104539 RMVar_ID_104539 Human_SNP_ID_616629568 m1A Human chr17 + 8173498 8173498 8173498 CAATCAGGGTGTTGCAAGTCCTGATTACGCAGAGACGTTAATCACGTTTCATGCATCTCCAATCA CAATCAGGGTGTTGCAAGTCCTGATTACGCAGGGACGTTAATCACGTTTCATGCATCTCCAATCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:8173476..8173500 26863196 MeRIP-seq:(Medium) rs754138120 Functional Loss SNV dbSNP153 33..33 33 - - - 104540 RMVar_ID_104540 Human_SNP_ID_616629569 m1A Human chr17 + 8173498 8173498 8173498 CAATCAGGGTGTTGCAAGTCCTGATTACGCAGAGACGTTAATCACGTTTCATGCATCTCCAATCA CAATCAGGGTGTTGCAAGTCCTGATTACGCAGTGACGTTAATCACGTTTCATGCATCTCCAATCA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:8173476..8173500 26863196 MeRIP-seq:(Medium) rs754138120 Functional Loss SNV dbSNP153 33..33 33 - - - 104541 RMVar_ID_104541 Human_SNP_ID_616630828 m1A Human chr17 - 8176345 8176345 8176345 CGTCTAGATTTGTCGGCTTGCGGGGAGACTTCAGGAGTCGCTGTCTCTGAACTTCCAGCCTCAGA CGTCTAGATTTGTCGGCTTGCGGGGAGACTTCGGGAGTCGCTGTCTCTGAACTTCCAGCCTCAGA T C TMEM107 Ensembl:ENSG00000179029 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8176253..8176346 26863196 MeRIP-seq:(Medium) rs535638789 Functional Loss SNV dbSNP153 33..33 33 - - - 104542 RMVar_ID_104542 Human_SNP_ID_616634614 m1A Human chr17 + 8187218 8187218 8187218 GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTCCGTGTTTCCCCCACGC GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGCATCCCAGCGGTGCCTCCGTGTTTCCCCCACGC A C LINC00324 RNACentral:URS0000D5828F lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1038167814 Functional Loss SNV dbSNP153 33..33 33 - - - 104543 RMVar_ID_104543 Human_SNP_ID_616634615 m1A Human chr17 + 8187218 8187218 8187218 GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTCCGTGTTTCCCCCACGC GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGGATCCCAGCGGTGCCTCCGTGTTTCCCCCACGC A G LINC00324 RNACentral:URS0000D5828F lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1038167814 Functional Loss SNV dbSNP153 33..33 33 - - - 104544 RMVar_ID_104544 Human_SNP_ID_616634663 m1A Human chr17 + 8187268 8187268 8187268 GTGTTTCCCCCACGCTTTTGCCAACATTAAACATTGTGAGGACAGTTGCAGAAACTCATAACTTC GTGTTTCCCCCACGCTTTTGCCAACATTAAACGTTGTGAGGACAGTTGCAGAAACTCATAACTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8187232..8187340 26863196 MeRIP-seq:(Medium) rs964820950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1871829,Human_RBP_ID_23129988 104545 RMVar_ID_104545 Human_SNP_ID_616634664 m1A Human chr17 - 8187270 8187270 8187270 TGGAAGTTATGAGTTTCTGCAACTGTCCTCACAATGTTTAATGTTGGCAAAAGCGTGGGGGAAAC TGGAAGTTATGAGTTTCTGCAACTGTCCTCACGATGTTTAATGTTGGCAAAAGCGTGGGGGAAAC T C LINC00324 RNACentral:URS0000D5828F lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:8187222..8187363 26863196 MeRIP-seq:(Medium) rs929447564 Functional Loss SNV dbSNP153 33..33 33 - - - 104546 RMVar_ID_104546 Human_SNP_ID_616634670 m1A Human chr17 - 8187294 8187294 8187294 GGTACGTGAGTAAACCATGTAGGATGGAAGTTATGAGTTTCTGCAACTGTCCTCACAATGTTTAA GGTACGTGAGTAAACCATGTAGGATGGAAGTTGTGAGTTTCTGCAACTGTCCTCACAATGTTTAA T C LINC00324 RNACentral:URS0000D5828F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8187243..8187343 26863196 MeRIP-seq:(Medium) rs535849796 Functional Loss SNV dbSNP153 33..33 33 - - - 104547 RMVar_ID_104547 Human_SNP_ID_616634921 m1A Human chr17 + 8187651 8187651 8187651 GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGATCCCCGTACGGGCCAGGATTGAAACTTTTCGA GTGGTGCTAATAACGCCAAGGTCGCGGGTTCGGTCCCCGTACGGGCCAGGATTGAAACTTTTCGA A G LINC00324 RNACentral:URS0000D5828F lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs750837159 Functional Loss SNV dbSNP153 33..33 33 - - - 104548 RMVar_ID_104548 Human_SNP_ID_616635409 m1A Human chr17 - 8189118 8189118 8189118 GCTCTGCAGCCGGTTCAGGGGCTGGCGCGCCAAGTCCGGGATATCCGACGTACTCTGGAGGTGTT GCTCTGCAGCCGGTTCAGGGGCTGGCGCGCCAGGTCCGGGATATCCGACGTACTCTGGAGGTGTT T C BORCS6 Ensembl:ENSG00000196544 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8189073..8189484 26863196 MeRIP-seq:(Medium) rs1378123530 Functional Loss SNV dbSNP153 33..33 33 - - - 104549 RMVar_ID_104549 Human_SNP_ID_616635420 m1A Human chr17 - 8189134 8189134 8189134 CGAGGAGCTGGAGCGGGCTCTGCAGCCGGTTCAGGGGCTGGCGCGCCAAGTCCGGGATATCCGAC CGAGGAGCTGGAGCGGGCTCTGCAGCCGGTTCGGGGGCTGGCGCGCCAAGTCCGGGATATCCGAC T C BORCS6 Ensembl:ENSG00000196544 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8189084..8189313 26863196 MeRIP-seq:(Medium) rs913598966 Functional Loss SNV dbSNP153 33..33 33 - - - 104550 RMVar_ID_104550 Human_SNP_ID_616635550 m1A Human chr17 + 8189463 8189463 8189463 GCAGAAGGCGGGGGTGGAGGCGCGCCGCTCAGACGGATCTTGAGTTGCAGGTTGTTGGCGACAAA GCAGAAGGCGGGGGTGGAGGCGCGCCGCTCAGTCGGATCTTGAGTTGCAGGTTGTTGGCGACAAA A T AC129492.7 Ensembl:ENSG00000279152 Other exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8189414..8189479 26863196 MeRIP-seq:(Medium) rs764827546 Functional Loss SNV dbSNP153 33..33 33 - - - 104551 RMVar_ID_104551 Human_SNP_ID_616635661 m1A Human chr17 + 8189730 8189730 8189730 TCCTCGTCGTTGTCTTCCTCCTCCTGCTGCTCAACATCCATCCCGCCGCCTGGTCCCCCTCGACG TCCTCGTCGTTGTCTTCCTCCTCCTGCTGCTCCACATCCATCCCGCCGCCTGGTCCCCCTCGACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8189546..8190166 26863196 MeRIP-seq:(Medium) rs1242187888 Functional Loss SNV dbSNP153 33..33 33 - - - 104552 RMVar_ID_104552 Human_SNP_ID_616639939 m1A Human chr17 + 8204873 8204873 8204873 CACACGCACCCGAGTGAATGACAGGGACCATCAGGCGACAGATTGAAGGGCAGAGGGAGGCAGCA CACACGCACCCGAGTGAATGACAGGGACCATCGGGCGACAGATTGAAGGGCAGAGGGAGGCAGCA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:8204826..8204973 26863196 MeRIP-seq:(Medium) rs1161457774 Functional Loss SNV dbSNP153 33..33 33 - - - 104553 RMVar_ID_104553 Human_SNP_ID_616639952 m1A Human chr17 + 8204902 8204901 8204902 ATCAGGCGACAGATTGAAGGGCAGAGGGAGGCAGCACCCTCCGAGAGTTGGCCCGGACCCAAGGG ATCAGGCGACAGATTGAAGGGCAGAGGGAGGC_GCACCCTCCGAGAGTTGGCCCGGACCCAAGGG CA C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:8204810..8204971 26863196 MeRIP-seq:(Medium) rs1352935270 Functional Loss DEL dbSNP153 33..33 33 - - - 104554 RMVar_ID_104554 Human_SNP_ID_616640895 m1A Human chr17 - 8207753 8207753 8207753 CCCCATCTGCACTTGTCCTCATGAGCCGCTCCAATGTCCAGCCCACAGGTAACTGGCGCAAGGGG CCCCATCTGCACTTGTCCTCATGAGCCGCTCCGATGTCCAGCCCACAGGTAACTGGCGCAAGGGG T C AURKB Ensembl:ENSG00000178999 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8207750..8207850 32194978 MeRIP-seq:(Medium) rs373303324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011320,Human_RBP_ID_1370421,Human_RBP_ID_1546334,Human_RBP_ID_13213273,Human_RBP_ID_17693442,Human_RBP_ID_18990478,Human_RBP_ID_19081496,Human_RBP_ID_26456854 Human_Splice_Rec_1776372,Human_Splice_Rec_1776373,Human_Splice_Rec_1776388,Human_Splice_Rec_1776389,Human_Splice_Rec_1776402,Human_Splice_Rec_1776403,Human_Splice_Rec_1776424,Human_Splice_Rec_1776425,Human_Splice_Rec_1776436,Human_Splice_Rec_1776437,Human_Splice_Rec_1776451,Human_Splice_Rec_1776464,Human_Splice_Rec_1776465,Human_Splice_Rec_1776473,Human_Splice_Rec_1776480,Human_Splice_Rec_1776481,Human_Splice_Rec_1776490,Human_Splice_Rec_1776491,Human_Splice_Rec_1776501 RMVar_hsa_circ_18761,RMVar_hsa_circ_281978,RMVar_hsa_circ_295441,RMVar_hsa_circ_115691,RMVar_hsa_circ_181996,RMVar_hsa_circ_181998 104555 RMVar_ID_104555 Human_SNP_ID_616641555 m1A Human chr17 + 8210079 8210079 8210079 GGACCCGTACTTTGGAGCATAACGGGGAAGAAAGTGCTTAAAGGATTGCTCATTGCAGGATCTCA GGACCCGTACTTTGGAGCATAACGGGGAAGAACGTGCTTAAAGGATTGCTCATTGCAGGATCTCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8210077..8210250 26863196 MeRIP-seq:(Medium) rs752966056 Functional Loss SNV dbSNP153 33..33 33 - - - 104556 RMVar_ID_104556 Human_SNP_ID_616641556 m1A Human chr17 + 8210079 8210079 8210079 GGACCCGTACTTTGGAGCATAACGGGGAAGAAAGTGCTTAAAGGATTGCTCATTGCAGGATCTCA GGACCCGTACTTTGGAGCATAACGGGGAAGAAGGTGCTTAAAGGATTGCTCATTGCAGGATCTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8210077..8210250 26863196 MeRIP-seq:(Medium) rs752966056 Functional Loss SNV dbSNP153 33..33 33 - - - 104557 RMVar_ID_104557 Human_SNP_ID_616641571 m1A Human chr17 + 8210134 8210134 8210134 CAGGATCTCAAGTTTCCCAGCAGGAACTCGCCATGCGGGGTCATGGGGGCGCAGGGACGGAGGGA CAGGATCTCAAGTTTCCCAGCAGGAACTCGCCCTGCGGGGTCATGGGGGCGCAGGGACGGAGGGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:8210126..8210250 26863196 MeRIP-seq:(Medium) rs775440600 Functional Loss SNV dbSNP153 33..33 33 - - - 104558 RMVar_ID_104558 Human_SNP_ID_616641572 m1A Human chr17 + 8210134 8210134 8210134 CAGGATCTCAAGTTTCCCAGCAGGAACTCGCCATGCGGGGTCATGGGGGCGCAGGGACGGAGGGA CAGGATCTCAAGTTTCCCAGCAGGAACTCGCCGTGCGGGGTCATGGGGGCGCAGGGACGGAGGGA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:8210126..8210250 26863196 MeRIP-seq:(Medium) rs775440600 Functional Loss SNV dbSNP153 33..33 33 - - - 104559 RMVar_ID_104559 Human_SNP_ID_616644675 m1A Human chr17 - 8220819 8220819 8220819 CCTAATCAAATAGACCTACGGTGACATTTTTCAGGATAGGAAAAAAAAAAAGCCTCCTCAGTAGA CCTAATCAAATAGACCTACGGTGACATTTTTCGGGATAGGAAAAAAAAAAAGCCTCCTCAGTAGA T C LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8220692..8220873 26863196 MeRIP-seq:(Medium) rs1212197963 Functional Loss SNV dbSNP153 33..33 33 - - - 104560 RMVar_ID_104560 Human_SNP_ID_616644952 m1A Human chr17 - 8221406 8221406 8221406 GCCGTCGTCTGCCCAGCGCGCAATTGTGAGTGACCTTCACCGCTAGCGCGCGCCACCCACCCCAC GCCGTCGTCTGCCCAGCGCGCAATTGTGAGTGTCCTTCACCGCTAGCGCGCGCCACCCACCCCAC T A LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8221370..8221501 26863196 MeRIP-seq:(Medium) rs973590549 Functional Loss SNV dbSNP153 33..33 33 - - - 104561 RMVar_ID_104561 Human_SNP_ID_616645144 m1A Human chr17 + 8221604 8221604 8221604 TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGATTCCCGGCCAACGCAAGTCGTTTTGGGTGTTT TAGCTGCCTTCCAAGCAGTTGACCCGGGTTCGTTTCCCGGCCAACGCAAGTCGTTTTGGGTGTTT A T LINC00324 Ensembl:ENSG00000178977 lincRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs112732934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4467537 104562 RMVar_ID_104562 Human_SNP_ID_616645472 m1A Human chr17 - 8222253 8222253 8222253 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGAGTACTAGCAGTTTTGA TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGAGTACTAGCAGTTTTGA T C LINC00324 Ensembl:ENSG00000178977 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1357563321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238414,Human_RBP_ID_278785,Human_RBP_ID_504070,Human_RBP_ID_763883,Human_RBP_ID_819952,Human_RBP_ID_901658,Human_RBP_ID_1011327,Human_RBP_ID_1185440,Human_RBP_ID_1370428,Human_RBP_ID_1546359,Human_RBP_ID_1871880,Human_RBP_ID_3540800,Human_RBP_ID_4467434,Human_RBP_ID_5088369,Human_RBP_ID_5097941,Human_RBP_ID_5184945,Human_RBP_ID_5260561,Human_RBP_ID_5649223,Human_RBP_ID_6666721,Human_RBP_ID_8194048,Human_RBP_ID_8255118,Human_RBP_ID_8467509,Human_RBP_ID_9077274,Human_RBP_ID_9326479,Human_RBP_ID_9424660,Human_RBP_ID_9882296,Human_RBP_ID_17081220,Human_RBP_ID_17126576,Human_RBP_ID_17264414,Human_RBP_ID_17582790,Human_RBP_ID_17903749,Human_RBP_ID_18165076,Human_RBP_ID_18544453,Human_RBP_ID_18545444,Human_RBP_ID_18713162,Human_RBP_ID_18943915,Human_RBP_ID_20287179,Human_RBP_ID_22524068,Human_RBP_ID_22544896,Human_RBP_ID_22585286,Human_RBP_ID_22808017,Human_RBP_ID_23130026,Human_RBP_ID_23757476,Human_RBP_ID_24559541,Human_RBP_ID_26749214,Human_RBP_ID_26758211,Human_RBP_ID_27572949,Human_RBP_ID_27670408 104563 RMVar_ID_104563 Human_SNP_ID_616645550 m1A Human chr17 - 8222301 8222301 8222301 CGGAGAAAGGTCTCTACAGGTCCCTCCTCGTTAGTATAGTGGTGAGTATCCCCGCCTGTCACGCG CGGAGAAAGGTCTCTACAGGTCCCTCCTCGTTGGTATAGTGGTGAGTATCCCCGCCTGTCACGCG T C LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1276181990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504071,Human_RBP_ID_1185441,Human_RBP_ID_1370429,Human_RBP_ID_1547588,Human_RBP_ID_1871881,Human_RBP_ID_2527723,Human_RBP_ID_3540801,Human_RBP_ID_5260562,Human_RBP_ID_5275011,Human_RBP_ID_5498137,Human_RBP_ID_5580054,Human_RBP_ID_6654672,Human_RBP_ID_8253915,Human_RBP_ID_8467511,Human_RBP_ID_8824059,Human_RBP_ID_9077275,Human_RBP_ID_13213396,Human_RBP_ID_17126576,Human_RBP_ID_17380437,Human_RBP_ID_17903750,Human_RBP_ID_18408746,Human_RBP_ID_18713164,Human_RBP_ID_18943915,Human_RBP_ID_20292358,Human_RBP_ID_23130028,Human_RBP_ID_23757478,Human_RBP_ID_26758212,Human_RBP_ID_27572949 Human_Splice_Rec_1776509 104564 RMVar_ID_104564 Human_SNP_ID_616645744 m1A Human chr17 - 8222808 8222808 8222808 ACGAGCCCTCCTTTACCTTTTACTGAGACAAGAGTGTCTTCAAGGAATAGGTTACCTGACCAGCG ACGAGCCCTCCTTTACCTTTTACTGAGACAAGGGTGTCTTCAAGGAATAGGTTACCTGACCAGCG T C LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8222473..8223049 26863196 MeRIP-seq:(Medium) rs1318678149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23130034 104565 RMVar_ID_104565 Human_SNP_ID_616645869 m1A Human chr17 - 8222939 8222939 8222939 AGTGGACCCAGCACTACAGCAAGCCTGGCACGACCTCTAAGGCGGTTCGCGGCAACGTCCGCACG AGTGGACCCAGCACTACAGCAAGCCTGGCACGGCCTCTAAGGCGGTTCGCGGCAACGTCCGCACG T C LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8222888..8223013 26863196 MeRIP-seq:(Medium) rs989286543 Functional Loss SNV dbSNP153 33..33 33 - - - 104566 RMVar_ID_104566 Human_SNP_ID_616645870 m1A Human chr17 - 8222939 8222939 8222939 AGTGGACCCAGCACTACAGCAAGCCTGGCACGACCTCTAAGGCGGTTCGCGGCAACGTCCGCACG AGTGGACCCAGCACTACAGCAAGCCTGGCACGCCCTCTAAGGCGGTTCGCGGCAACGTCCGCACG T G LINC00324 Ensembl:ENSG00000178977 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8222888..8223013 26863196 MeRIP-seq:(Medium) rs989286543 Functional Loss SNV dbSNP153 33..33 33 - - - 104567 RMVar_ID_104567 Human_SNP_ID_616646772 m1A Human chr17 + 8226147 8226147 8226147 CTCTGCAGGAAATGTGGGTGCTATGAGTGCAGAACAGAAACTCTTACGCGTTCTGATATAAAAAC CTCTGCAGGAAATGTGGGTGCTATGAGTGCAGTACAGAAACTCTTACGCGTTCTGATATAAAAAC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:8226045..8226237 26863410 MeRIP-seq:(Medium) rs1390457936 Functional Loss SNV dbSNP153 33..33 33 - - - 104568 RMVar_ID_104568 Human_SNP_ID_616646780 m1A Human chr17 + 8226160 8226160 8226160 GTGGGTGCTATGAGTGCAGAACAGAAACTCTTACGCGTTCTGATATAAAAACAATACATGAAAGG GTGGGTGCTATGAGTGCAGAACAGAAACTCTTCCGCGTTCTGATATAAAAACAATACATGAAAGG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:8226066..8226237 26863410 MeRIP-seq:(Medium) rs878901998 Functional Loss SNV dbSNP153 33..33 33 - - - 104569 RMVar_ID_104569 Human_SNP_ID_616646781 m1A Human chr17 + 8226160 8226160 8226160 GTGGGTGCTATGAGTGCAGAACAGAAACTCTTACGCGTTCTGATATAAAAACAATACATGAAAGG GTGGGTGCTATGAGTGCAGAACAGAAACTCTTGCGCGTTCTGATATAAAAACAATACATGAAAGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:8226066..8226237 26863410 MeRIP-seq:(Medium) rs878901998 Functional Loss SNV dbSNP153 33..33 33 - - - 104570 RMVar_ID_104570 Human_SNP_ID_616646802 m1A Human chr17 + 8226189 8226189 8226189 CTTACGCGTTCTGATATAAAAACAATACATGAAAGGATGTGGATTTAGCCGCAAAATCACGCTGT CTTACGCGTTCTGATATAAAAACAATACATGAGAGGATGTGGATTTAGCCGCAAAATCACGCTGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8226119..8226231 26863196 MeRIP-seq:(Medium) rs918150796 Functional Loss SNV dbSNP153 33..33 33 - - - 104571 RMVar_ID_104571 Human_SNP_ID_616646817 m1A Human chr17 - 8226213 8226213 8226213 CAGCGGTGCCTTTATTCAATTGAAACAGCGTGATTTTGCGGCTAAATCCACATCCTTTCATGTAT CAGCGGTGCCTTTATTCAATTGAAACAGCGTGGTTTTGCGGCTAAATCCACATCCTTTCATGTAT T C CTC1 Ensembl:ENSG00000178971 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8226065..8226230 26863196 MeRIP-seq:(Medium) rs1291320361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134231,Human_RBP_ID_23130042 104572 RMVar_ID_104572 Human_SNP_ID_616646858 m1A Human chr17 - 8226250 8226250 8226250 GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGAATCCCAGCGGTGCCTTTATTCAATTGAAACAG GCCTGTCTAGTAAACAGGAGATCCTGGGTTCGGATCCCAGCGGTGCCTTTATTCAATTGAAACAG T C CTC1 Ensembl:ENSG00000178971 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs780992571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134231,Human_RBP_ID_504072,Human_RBP_ID_5186458,Human_RBP_ID_5260477,Human_RBP_ID_9077276,Human_RBP_ID_17006847,Human_RBP_ID_17126578,Human_RBP_ID_17903752,Human_RBP_ID_18486353,Human_RBP_ID_21889923,Human_RBP_ID_22531544,Human_RBP_ID_22760705,Human_RBP_ID_23130043,Human_RBP_ID_24531904,Human_RBP_ID_26976856,Human_RBP_ID_27263701 Human_miRNA_ID_1495718 Clinvar_Rec_668 104573 RMVar_ID_104573 Human_SNP_ID_616647109 m1A Human chr17 - 8226625 8226625 8226625 GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGAATCCTGCCGACTACGTCATATTTTTTTCTTCA GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGGATCCTGCCGACTACGTCATATTTTTTTCTTCA T C CTC1 Ensembl:ENSG00000178971 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs761442327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6205,Human_RBP_ID_262575,Human_RBP_ID_1370430,Human_RBP_ID_1546366,Human_RBP_ID_4464326,Human_RBP_ID_5143467,Human_RBP_ID_5237587,Human_RBP_ID_5275183,Human_RBP_ID_5318257,Human_RBP_ID_6654676,Human_RBP_ID_8192696,Human_RBP_ID_8467518,Human_RBP_ID_9077277,Human_RBP_ID_9326481,Human_RBP_ID_9341006,Human_RBP_ID_17128073,Human_RBP_ID_17380433,Human_RBP_ID_18200290,Human_RBP_ID_18420470,Human_RBP_ID_18439978,Human_RBP_ID_18544396,Human_RBP_ID_18545429,Human_RBP_ID_18713175,Human_RBP_ID_19084962,Human_RBP_ID_21889924,Human_RBP_ID_21908665,Human_RBP_ID_22531550,Human_RBP_ID_22544227,Human_RBP_ID_22587588,Human_RBP_ID_22740847,Human_RBP_ID_22761047,Human_RBP_ID_22807784,Human_RBP_ID_23130048,Human_RBP_ID_23757483,Human_RBP_ID_24481764,Human_RBP_ID_24531905,Human_RBP_ID_26769471,Human_RBP_ID_26976859,Human_RBP_ID_27572795 104574 RMVar_ID_104574 Human_SNP_ID_616647231 m1A Human chr17 - 8226732 8226732 8226732 TTTCATGGAGGCAGATGTTTGTCAGTCAAGGGAAGTAAGAAAGGCATTGGATGAAAACGAAGCCC TTTCATGGAGGCAGATGTTTGTCAGTCAAGGGGAGTAAGAAAGGCATTGGATGAAAACGAAGCCC T C CTC1 Ensembl:ENSG00000178971 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8226683..8227112 26863196 MeRIP-seq:(Medium) rs973494054 Functional Loss SNV dbSNP153 33..33 33 - - - 104575 RMVar_ID_104575 Human_SNP_ID_616647241 m1A Human chr17 - 8226752 8226752 8226752 TCTTTTTTTCCCTGAAGCGCTTTCATGGAGGCAGATGTTTGTCAGTCAAGGGAAGTAAGAAAGGC TCTTTTTTTCCCTGAAGCGCTTTCATGGAGGCGGATGTTTGTCAGTCAAGGGAAGTAAGAAAGGC T C CTC1 Ensembl:ENSG00000178971 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8226702..8226783 26863196 MeRIP-seq:(Medium) rs1270625341 Functional Loss SNV dbSNP153 33..33 33 - - - 104576 RMVar_ID_104576 Human_SNP_ID_616647515 m1A Human chr17 + 8227094 8227094 8227094 GCCACTAACTTTCCGGGTCTACTTCAAATCTTAATATAGGGTATTGCTACCATAAAAGCAGCATA GCCACTAACTTTCCGGGTCTACTTCAAATCTTCATATAGGGTATTGCTACCATAAAAGCAGCATA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8227044..8227161 26863196 MeRIP-seq:(Medium) rs1056311504 Functional Loss SNV dbSNP153 33..33 33 - - - 104577 RMVar_ID_104577 Human_SNP_ID_616654392 m1A Human chr17 - 8249332 8249332 8249332 GTCCGCACGCGGTAACTATACTCACGTGGAAGATGCACTCGCGGCCACAGAGCACCTCGAATCGT GTCCGCACGCGGTAACTATACTCACGTGGAAGGTGCACTCGCGGCCACAGAGCACCTCGAATCGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8249319..8249406 26863196 MeRIP-seq:(Medium) rs991715716 Functional Loss SNV dbSNP153 33..33 33 - - - 104578 RMVar_ID_104578 Human_SNP_ID_616654393 m1A Human chr17 - 8249332 8249332 8249332 GTCCGCACGCGGTAACTATACTCACGTGGAAGATGCACTCGCGGCCACAGAGCACCTCGAATCGT GTCCGCACGCGGTAACTATACTCACGTGGAAGCTGCACTCGCGGCCACAGAGCACCTCGAATCGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8249319..8249406 26863196 MeRIP-seq:(Medium) rs991715716 Functional Loss SNV dbSNP153 33..33 33 - - - 104579 RMVar_ID_104579 Human_SNP_ID_616654394 m1A Human chr17 + 8249338 8249338 8249338 CGAGGTGCTCTGTGGCCGCGAGTGCATCTTCCACGTGAGTATAGTTACCGCGTGCGGACCTGGAT CGAGGTGCTCTGTGGCCGCGAGTGCATCTTCCGCGTGAGTATAGTTACCGCGTGCGGACCTGGAT A G PFAS Ensembl:ENSG00000178921 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8249313..8249395 26863196 MeRIP-seq:(Medium) rs1182938812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19078363 Human_Splice_Rec_1776751,Human_Splice_Rec_1776759,Human_Splice_Rec_1776809 104580 RMVar_ID_104580 Human_SNP_ID_616655583 m1A Human chr17 - 8253854 8253854 8253854 TCCTTTGCTGGAGAGATGAATTAGGTTCCTAAAAAATAACATTAACTAAGCCGGGCGTGGTGGCT TCCTTTGCTGGAGAGATGAATTAGGTTCCTAAGAAATAACATTAACTAAGCCGGGCGTGGTGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8253851..8253990 26863196 MeRIP-seq:(Medium) rs918480181 Functional Loss SNV dbSNP153 33..33 33 - - - 104581 RMVar_ID_104581 Human_SNP_ID_616655630 m1A Human chr17 + 8253981 8253981 8253981 CCTTCACTTCTATGTTCGTCCCTCTGGCCATGAGGGGGCAGCCCCTGGACACACTCGGAGGAAAC CCTTCACTTCTATGTTCGTCCCTCTGGCCATGCGGGGGCAGCCCCTGGACACACTCGGAGGAAAC A C PFAS Ensembl:ENSG00000178921 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8253931..8255660 32194978 MeRIP-seq:(Medium) rs758832526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3950108,Human_RBP_ID_9375326,Human_RBP_ID_17262575,Human_RBP_ID_22443454,Human_RBP_ID_26811934 Human_Splice_Rec_1776749,Human_Splice_Rec_1776753,Human_Splice_Rec_1776761,Human_Splice_Rec_1776811,Human_Splice_Rec_1776865,Human_Splice_Rec_1776869 Human_miRNA_ID_2152043,Human_miRNA_ID_2420509 RMVar_hsa_circ_182014,RMVar_hsa_circ_315975,RMVar_hsa_circ_365497 104582 RMVar_ID_104582 Human_SNP_ID_616656951 m1A Human chr17 - 8257940 8257940 8257940 GGGTGTTTGTCATCCCTCCACACCCCAGCCTCACCAGCCAGCACTGGTTCCCCAAACTTGTTGCC GGGTGTTTGTCATCCCTCCACACCCCAGCCTCCCCAGCCAGCACTGGTTCCCCAAACTTGTTGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8257903..8258186 32194978 MeRIP-seq:(Medium) rs754696204 Functional Loss SNV dbSNP153 33..33 33 - - - 104583 RMVar_ID_104583 Human_SNP_ID_616658943 m1A Human chr17 - 8264510 8264510 8264510 CCTGGTGCACGCTCAGCCCTGGGGGCAAGGCCAGAGGCTGCAGCATGGGGGGCTTCCTCTGCAGG CCTGGTGCACGCTCAGCCCTGGGGGCAAGGCCTGAGGCTGCAGCATGGGGGGCTTCCTCTGCAGG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:8264201..8264550 26863196 MeRIP-seq:(Medium) rs1203577910 Functional Loss SNV dbSNP153 33..33 33 - - - 104584 RMVar_ID_104584 Human_SNP_ID_616659739 m1A Human chr17 + 8266781 8266781 8266781 CCAGTCCTGTCTGTGCTGTTCGCTGAGGAGCCAGGCCTCGTGCTGGAGGTGCAGGAGCCAGACCT CCAGTCCTGTCTGTGCTGTTCGCTGAGGAGCCCGGCCTCGTGCTGGAGGTGCAGGAGCCAGACCT A C PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8266762..8266863 32194978 MeRIP-seq:(Medium) rs764751135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905323,Human_RBP_ID_13213731,Human_RBP_ID_18987919,Human_RBP_ID_22443462,Human_RBP_ID_22544232,Human_RBP_ID_23118852 Human_Splice_Rec_1776798,Human_Splice_Rec_1776852,Human_Splice_Rec_1776908,Human_Splice_Rec_1776918 RMVar_hsa_circ_42509,RMVar_hsa_circ_95909,RMVar_hsa_circ_182020,RMVar_hsa_circ_116556,RMVar_hsa_circ_182022,RMVar_hsa_circ_2681,RMVar_hsa_circ_75986,RMVar_hsa_circ_182024,RMVar_hsa_circ_374739,RMVar_hsa_circ_182027 104585 RMVar_ID_104585 Human_SNP_ID_616660700 m1A Human chr17 - 8269012 8269012 8269012 GGGTTCCCGTCATCATCAGCCCAGTGCAGTGGAGCCAAGCCCCTGGCCTCAATCTGAGCTTGGAG GGGTTCCCGTCATCATCAGCCCAGTGCAGTGGGGCCAAGCCCCTGGCCTCAATCTGAGCTTGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8268947..8269147 32194978 MeRIP-seq:(Medium) rs1444144658 Functional Loss SNV dbSNP153 33..33 33 - - - 104586 RMVar_ID_104586 Human_SNP_ID_616660868 m1A Human chr17 + 8269520 8269520 8269520 GCCCAGGAAACAGCATGTGGTTCAGAGAAAAGAGCGACAAGGAAAAGTTAGGACTCCTGAGGTCC GCCCAGGAAACAGCATGTGGTTCAGAGAAAAGGGCGACAAGGAAAAGTTAGGACTCCTGAGGTCC A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8269333..8269600 26863196 MeRIP-seq:(Medium) rs1017618639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504090,Human_RBP_ID_1871908,Human_RBP_ID_13213774 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 104587 RMVar_ID_104587 Human_SNP_ID_616667617 m1A Human chr17 - 8294991 8294991 8294991 ATCTCTTCCCTGCTTGCCAGCTCTTGACTCCCAAATTCCAGCTGACGTTTGACCACTTGACATTT ATCTCTTCCCTGCTTGCCAGCTCTTGACTCCCCAATTCCAGCTGACGTTTGACCACTTGACATTT T G SLC25A35 Ensembl:ENSG00000125434 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:8294951..8295025 26863196 MeRIP-seq:(Medium) rs1157116152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20287554 104588 RMVar_ID_104588 Human_SNP_ID_616667628 m1A Human chr17 - 8295031 8295031 8295031 GTCCTGCCTTAAGCTTCTCACCAGAATCTCCTAGATTTCTATCTCTTCCCTGCTTGCCAGCTCTT GTCCTGCCTTAAGCTTCTCACCAGAATCTCCTGGATTTCTATCTCTTCCCTGCTTGCCAGCTCTT T C SLC25A35 Ensembl:ENSG00000125434 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:8294980..8295232 26863196 MeRIP-seq:(Medium) rs552263770 Functional Loss SNV dbSNP153 33..33 33 - - - 104589 RMVar_ID_104589 Human_SNP_ID_616689884 m1A Human chr17 - 8377618 8377618 8377618 ATCCTCGAACGGAAAGCCAAATCTCGCCAAGTAGGAAAGGAAAAGGGCAAATACAAGGAAGAAAC ATCCTCGAACGGAAAGCCAAATCTCGCCAAGTTGGAAAGGAAAAGGGCAAATACAAGGAAGAAAC T A RPL26,AC135178.3 Ensembl:ENSG00000161970,Ensembl:ENSG00000263809 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8377552..8377693 26863196 MeRIP-seq:(Medium) rs201307266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237990,Human_RBP_ID_504172,Human_RBP_ID_1546497,Human_RBP_ID_1871956,Human_RBP_ID_2527841,Human_RBP_ID_3540884,Human_RBP_ID_8467610,Human_RBP_ID_9077292,Human_RBP_ID_10483487,Human_RBP_ID_13214919,Human_RBP_ID_17262601,Human_RBP_ID_17495078,Human_RBP_ID_22958933,Human_RBP_ID_26456875 Human_Splice_Rec_1777192,Human_Splice_Rec_1777198,Human_Splice_Rec_1777204,Human_Splice_Rec_1777210,Human_Splice_Rec_1777212,Human_Splice_Rec_1777218,Human_Splice_Rec_1777224,Human_Splice_Rec_1777230,Human_Splice_Rec_1777236 RMVar_hsa_circ_16592 104590 RMVar_ID_104590 Human_SNP_ID_616689885 m1A Human chr17 - 8377618 8377618 8377618 ATCCTCGAACGGAAAGCCAAATCTCGCCAAGTAGGAAAGGAAAAGGGCAAATACAAGGAAGAAAC ATCCTCGAACGGAAAGCCAAATCTCGCCAAGTGGGAAAGGAAAAGGGCAAATACAAGGAAGAAAC T C RPL26,AC135178.3 Ensembl:ENSG00000161970,Ensembl:ENSG00000263809 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8377552..8377693 26863196 MeRIP-seq:(Medium) rs201307266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237990,Human_RBP_ID_504172,Human_RBP_ID_1546497,Human_RBP_ID_1871956,Human_RBP_ID_2527841,Human_RBP_ID_3540884,Human_RBP_ID_8467610,Human_RBP_ID_9077292,Human_RBP_ID_10483487,Human_RBP_ID_13214919,Human_RBP_ID_17262601,Human_RBP_ID_17495078,Human_RBP_ID_22958933,Human_RBP_ID_26456875 Human_Splice_Rec_1777192,Human_Splice_Rec_1777198,Human_Splice_Rec_1777204,Human_Splice_Rec_1777210,Human_Splice_Rec_1777212,Human_Splice_Rec_1777218,Human_Splice_Rec_1777224,Human_Splice_Rec_1777230,Human_Splice_Rec_1777236 RMVar_hsa_circ_16592 104591 RMVar_ID_104591 Human_SNP_ID_616691484 m1A Human chr17 - 8382970 8382970 8382970 CAAGGGCCGCCGGGCCGGAGATGGATGGAGGGACCGGGGATTTGGGAACTCGAAAACGAGCTGAG CAAGGGCCGCCGGGCCGGAGATGGATGGAGGGGCCGGGGATTTGGGAACTCGAAAACGAGCTGAG T C RPL26,AC135178.3 Ensembl:ENSG00000161970,Ensembl:ENSG00000263809 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8382965..8383175 26863196 MeRIP-seq:(Medium) rs1333282434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237996,Human_RBP_ID_504189,Human_RBP_ID_767239,Human_RBP_ID_1289857,Human_RBP_ID_4463267,Human_RBP_ID_5467284,Human_RBP_ID_6655072,Human_RBP_ID_13215233,Human_RBP_ID_23757712 RMVar_hsa_circ_4272 104592 RMVar_ID_104592 Human_SNP_ID_616691486 m1A Human chr17 + 8382977 8382973 8382977 CGTTTTCGAGTTCCCAAATCCCCGGTCCCTCCATCCATCTCCGGCCCGGCGGCCCTTGATTTAAG CGTTTTCGAGTTCCCAAATCCCCGGTCCC____TCCATCTCCGGCCCGGCGGCCCTTGATTTAAG CTCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8382951..8383200 26863196 MeRIP-seq:(Medium) rs1235743319 Functional Loss DEL dbSNP153 30..33 33 - - - 104593 RMVar_ID_104593 Human_SNP_ID_616691509 m1A Human chr17 + 8383065 8383062 8383065 CCAGTCTCTCCTTCCTGGCTGCTACTCGGCCGACAAGAGACTCTCGGGGTCCCCGCGGTCGGAAG CCAGTCTCTCCTTCCTGGCTGCTACTCGGC___CAAGAGACTCTCGGGGTCCCCGCGGTCGGAAG CCGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:8383047..8383169 26863410 MeRIP-seq:(Medium) rs1177475844 Functional Loss DEL dbSNP153 31..33 33 - - - 104594 RMVar_ID_104594 Human_SNP_ID_616705176 m1A Human chr17 - 8435936 8435936 8435936 GCCGCTCGGCTCAGCTCCCCTACGCAGCCCCGAGCTCCACTCAGCGTACCTCCGCGCCCGGCTCC GCCGCTCGGCTCAGCTCCCCTACGCAGCCCCGCGCTCCACTCAGCGTACCTCCGCGCCCGGCTCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:8435901..8436066 26863196 MeRIP-seq:(Medium) rs1445518713 Functional Loss SNV dbSNP153 33..33 33 - - - 104595 RMVar_ID_104595 Human_SNP_ID_616705191 m1A Human chr17 + 8435948 8435948 8435948 GGAGGTACGCTGAGTGGAGCTCGGGGCTGCGTAGGGGAGCTGAGCCGAGCGGCTGGGCGGGCCTG GGAGGTACGCTGAGTGGAGCTCGGGGCTGCGTGGGGGAGCTGAGCCGAGCGGCTGGGCGGGCCTG A G NDEL1 Ensembl:ENSG00000166579 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8435901..8436180 26863196 MeRIP-seq:(Medium) rs1338709641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767248,Human_RBP_ID_4463290,Human_RBP_ID_18469985 Human_Splice_Rec_1777275,Human_Splice_Rec_1777283,Human_Splice_Rec_1777299,Human_Splice_Rec_1777303,Human_Splice_Rec_1777317,Human_Splice_Rec_1777335,Human_Splice_Rec_1777339,Human_Splice_Rec_1777345,Human_Splice_Rec_1777349 104596 RMVar_ID_104596 Human_SNP_ID_616705239 m1A Human chr17 + 8435999 8435999 8435999 GCTGGGCGGGCCTGGCCGGGCCGGCGGAGGGGAGACGTCGGTTGAGCGGCGGCGAACATGCGCTT GCTGGGCGGGCCTGGCCGGGCCGGCGGAGGGGGGACGTCGGTTGAGCGGCGGCGAACATGCGCTT A G NDEL1 Ensembl:ENSG00000166579 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8435876..8436056 26863196 MeRIP-seq:(Medium) rs780070964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238002,Human_RBP_ID_767249,Human_RBP_ID_4463293,Human_RBP_ID_5237866,Human_RBP_ID_18469985,Human_RBP_ID_26458708,Human_RBP_ID_26769270 Human_Splice_Rec_1777275,Human_Splice_Rec_1777283,Human_Splice_Rec_1777299,Human_Splice_Rec_1777303,Human_Splice_Rec_1777317,Human_Splice_Rec_1777335,Human_Splice_Rec_1777339,Human_Splice_Rec_1777345,Human_Splice_Rec_1777349 104597 RMVar_ID_104597 Human_SNP_ID_616705336 m1A Human chr17 + 8436255 8436255 8436255 CCTCCCTTCCCTGGTCCGATGTGTGGCCCCCCAGGGGCGCCTGCAAGGGAACGATTCCGGTGGCC CCTCCCTTCCCTGGTCCGATGTGTGGCCCCCCTGGGGCGCCTGCAAGGGAACGATTCCGGTGGCC A T NDEL1 Ensembl:ENSG00000166579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:8436247..8436381;chr17:8436237..8436391 26863196 MeRIP-seq:(Medium) rs1431338344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5363757,Human_RBP_ID_26781122 104598 RMVar_ID_104598 Human_SNP_ID_616712108 m1A Human chr17 + 8464787 8464787 8464787 GGCCTGGGCATCTGGAGGCAGCTGTGGCCCCGACTTCCCCATCAGTGGCTCACTAGGTGAGCCTA GGCCTGGGCATCTGGAGGCAGCTGTGGCCCCGGCTTCCCCATCAGTGGCTCACTAGGTGAGCCTA A G NDEL1 Ensembl:ENSG00000166579 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:8464781..8464866 32194978 MeRIP-seq:(Medium) rs891224999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238007,Human_RBP_ID_13215951,Human_RBP_ID_17127042,Human_RBP_ID_22474972,Human_RBP_ID_23230017 104599 RMVar_ID_104599 Human_SNP_ID_616712775 m1A Human chr17 - 8467336 8467336 8467336 CTATCAGTACAGCAGAGTGGGGGCTATGGGGCAGGTGTGATGAATGGGTACTTCTGCATCCAGTG CTATCAGTACAGCAGAGTGGGGGCTATGGGGCTGGTGTGATGAATGGGTACTTCTGCATCCAGTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8467287..8467601 26863196 MeRIP-seq:(Medium) rs1485403174 Functional Loss SNV dbSNP153 33..33 33 - - - 104600 RMVar_ID_104600 Human_SNP_ID_616714814 m1A Human chr17 + 8475100 8475100 8475100 CTGCCACCTGGGGCCTCAGCTGCAGTGTGGCCACTATCCCTTCTATGCACAGACCAGCCCTCGCC CTGCCACCTGGGGCCTCAGCTGCAGTGTGGCCGCTATCCCTTCTATGCACAGACCAGCCCTCGCC A G NDEL1 Ensembl:ENSG00000166579 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:8475050..8475250 32194978 MeRIP-seq:(Medium) rs76429053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22717359 GWAS_ID_13695 104601 RMVar_ID_104601 Human_SNP_ID_616715867 m1A Human chr17 - 8478412 8478412 8478412 AACGAGCAGCCGCCAACAAATTAGTCCGTCGCACTGAGAAGAAGCTGAAAGAAATCTTCATGCAG AACGAGCAGCCGCCAACAAATTAGTCCGTCGCGCTGAGAAGAAGCTGAAAGAAATCTTCATGCAG T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8478363..8478479 26863196 MeRIP-seq:(Medium) rs773763080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1872032,Human_RBP_ID_4481865,Human_RBP_ID_13216326 Human_Splice_Rec_1777460,Human_Splice_Rec_1777461,Human_Splice_Rec_1777540,Human_Splice_Rec_1777541,Human_Splice_Rec_1777622,Human_Splice_Rec_1777623,Human_Splice_Rec_1777632 RMVar_hsa_circ_84961,RMVar_hsa_circ_182037 104602 RMVar_ID_104602 Human_SNP_ID_616718433 m1A Human chr17 - 8487558 8487558 8487558 GGGAGCTCGAGGCGGAGCTGGAGGATGAGAGGAAACAGCGGGCGCTTGCTGTAGCTTCAAAGAAA GGGAGCTCGAGGCGGAGCTGGAGGATGAGAGGCAACAGCGGGCGCTTGCTGTAGCTTCAAAGAAA T G MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8487507..8487651 26863196 MeRIP-seq:(Medium) rs1567780808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48032,Human_RBP_ID_899401,Human_RBP_ID_8824429,Human_RBP_ID_9375340,Human_RBP_ID_17903932,Human_RBP_ID_19078383,Human_RBP_ID_27812275 Human_Splice_Rec_1777450,Human_Splice_Rec_1777530,Human_Splice_Rec_1777612 RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_102710,RMVar_hsa_circ_182038,RMVar_hsa_circ_47841,RMVar_hsa_circ_375995,RMVar_hsa_circ_182039,RMVar_hsa_circ_268984,RMVar_hsa_circ_182040 104603 RMVar_ID_104603 Human_SNP_ID_616719950 m1A Human chr17 - 8492876 8492871 8492877 GGCACTGGCGTATGACAAACTGGAGAAGACCAAGAACCGCCTGCAGCAGGAGCTGGACGACCTCA GGCACTGGCGTATGACAAACTGGAGAAGACC______CGCCTGCAGCAGGAGCTGGACGACCTCA GGTTCTT G MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8492825..8493025 26863196 MeRIP-seq:(Medium) rs867830190 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_904599,Human_RBP_ID_5648798,Human_RBP_ID_8825321,Human_RBP_ID_9288780,Human_RBP_ID_9375349,Human_RBP_ID_17904686,Human_RBP_ID_18987927,Human_RBP_ID_24544776,Human_RBP_ID_27812278 Human_miRNA_ID_2512884,Human_miRNA_ID_3055707 RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_68821,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071 104604 RMVar_ID_104604 Human_SNP_ID_616719953 m1A Human chr17 - 8492876 8492876 8492876 GGCACTGGCGTATGACAAACTGGAGAAGACCAAGAACCGCCTGCAGCAGGAGCTGGACGACCTCA GGCACTGGCGTATGACAAACTGGAGAAGACCAGGAACCGCCTGCAGCAGGAGCTGGACGACCTCA T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8492825..8493025 26863196 MeRIP-seq:(Medium) rs372919713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_904599,Human_RBP_ID_5648798,Human_RBP_ID_8825321,Human_RBP_ID_9288780,Human_RBP_ID_9375349,Human_RBP_ID_17904686,Human_RBP_ID_18987927,Human_RBP_ID_24544776,Human_RBP_ID_27812278 Human_miRNA_ID_2512884,Human_miRNA_ID_3055707 RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_68821,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071 104605 RMVar_ID_104605 Human_SNP_ID_616720203 m1A Human chr17 - 8493782 8493776 8493782 GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGG______CCAGGAAGAACCTGGAGAAGCAAGTGC GCCTCCT G MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8493682..8493929 26863196 MeRIP-seq:(Medium) rs146612839 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_26977188,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104606 RMVar_ID_104606 Human_SNP_ID_616720204 m1A Human chr17 - 8493782 8493776 8493782 GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGG___AGGCCAGGAAGAACCTGGAGAAGCAAGTGC GCCTCCT GCCT MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8493682..8493929 26863196 MeRIP-seq:(Medium) rs146612839 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_26977188,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104607 RMVar_ID_104607 Human_SNP_ID_616720208 m1A Human chr17 - 8493782 8493782 8493782 GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGTGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC T A MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8493682..8493929 26863196 MeRIP-seq:(Medium) rs923511196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_26977188,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104608 RMVar_ID_104608 Human_SNP_ID_616720209 m1A Human chr17 - 8493782 8493782 8493782 GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC GAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGGGGAGGCCAGGAAGAACCTGGAGAAGCAAGTGC T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8493682..8493929 26863196 MeRIP-seq:(Medium) rs923511196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_26977188,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104609 RMVar_ID_104609 Human_SNP_ID_616720211 m1A Human chr17 - 8493785 8493785 8493785 GAAGAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAG GAAGAACAGTCTTCAGGAGCAGCAGGAGGAGGGGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAG T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:8493698..8493900;chr17:8493694..8493850 26863196 MeRIP-seq:(Medium) rs767113622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104610 RMVar_ID_104610 Human_SNP_ID_616720212 m1A Human chr17 - 8493785 8493785 8493785 GAAGAACAGTCTTCAGGAGCAGCAGGAGGAGGAGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAG GAAGAACAGTCTTCAGGAGCAGCAGGAGGAGGCGGAGGAGGCCAGGAAGAACCTGGAGAAGCAAG T G MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:8493698..8493900;chr17:8493694..8493850 26863196 MeRIP-seq:(Medium) rs767113622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48038,Human_RBP_ID_820329,Human_RBP_ID_899406,Human_RBP_ID_5114548,Human_RBP_ID_8253926,Human_RBP_ID_9288782,Human_RBP_ID_9375353,Human_RBP_ID_17653758,Human_RBP_ID_18411990,Human_RBP_ID_26330655,Human_RBP_ID_27812280 Human_Splice_Rec_1777443,Human_Splice_Rec_1777523,Human_Splice_Rec_1777605,Human_Splice_Rec_1777633 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_268984,RMVar_hsa_circ_70779,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_283311,RMVar_hsa_circ_364037,RMVar_hsa_circ_182042 104611 RMVar_ID_104611 Human_SNP_ID_616722089 m1A Human chr17 - 8500923 8500923 8500923 AGAAGTGGCAGAGCTGAAGAAAGCTCTTGAGGAGGAAACTAAGAACCATGAAGCTCAAATCCAGG AGAAGTGGCAGAGCTGAAGAAAGCTCTTGAGGCGGAAACTAAGAACCATGAAGCTCAAATCCAGG T G MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8500780..8501003 26863196 MeRIP-seq:(Medium) rs756915293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1872057,Human_RBP_ID_2528073,Human_RBP_ID_3540997,Human_RBP_ID_5467356,Human_RBP_ID_9288786,Human_RBP_ID_9375358,Human_RBP_ID_18531017,Human_RBP_ID_22715952,Human_RBP_ID_24552244,Human_RBP_ID_26331270,Human_RBP_ID_26813183,Human_RBP_ID_27812281 Human_Splice_Rec_1777436,Human_Splice_Rec_1777437,Human_Splice_Rec_1777516,Human_Splice_Rec_1777517,Human_Splice_Rec_1777598,Human_Splice_Rec_1777599 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_364037,RMVar_hsa_circ_26983,RMVar_hsa_circ_119481,RMVar_hsa_circ_314872,RMVar_hsa_circ_182043,RMVar_hsa_circ_105459,RMVar_hsa_circ_115357,RMVar_hsa_circ_182044,RMVar_hsa_circ_182045 104612 RMVar_ID_104612 Human_SNP_ID_616722090 m1A Human chr17 - 8500926 8500926 8500926 ACAAGAAGTGGCAGAGCTGAAGAAAGCTCTTGAGGAGGAAACTAAGAACCATGAAGCTCAAATCC ACAAGAAGTGGCAGAGCTGAAGAAAGCTCTTGTGGAGGAAACTAAGAACCATGAAGCTCAAATCC T A MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:8500876..8501010;chr17:8500876..8501008 26863196 MeRIP-seq:(Medium) rs1332447033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1872057,Human_RBP_ID_2528073,Human_RBP_ID_3540997,Human_RBP_ID_5467356,Human_RBP_ID_9288786,Human_RBP_ID_9375358,Human_RBP_ID_22715952,Human_RBP_ID_22958998,Human_RBP_ID_26331270,Human_RBP_ID_26813183,Human_RBP_ID_27812281 Human_Splice_Rec_1777436,Human_Splice_Rec_1777516,Human_Splice_Rec_1777598 Human_miRNA_ID_2438919 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_364037,RMVar_hsa_circ_26983,RMVar_hsa_circ_119481,RMVar_hsa_circ_314872,RMVar_hsa_circ_182043,RMVar_hsa_circ_105459,RMVar_hsa_circ_115357,RMVar_hsa_circ_182044,RMVar_hsa_circ_182045 104613 RMVar_ID_104613 Human_SNP_ID_616724263 m1A Human chr17 - 8509924 8509924 8509924 TCACAAGGACCTGGAAGAACAGCTAGACGAGGAGGAAGGGGCTCGGCAAAAGCTGCAGCTGGAAA TCACAAGGACCTGGAAGAACAGCTAGACGAGGGGGAAGGGGCTCGGCAAAAGCTGCAGCTGGAAA T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8509819..8509925 32194978 MeRIP-seq:(Medium) rs980413181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6709,Human_RBP_ID_48052,Human_RBP_ID_9288789,Human_RBP_ID_9375364,Human_RBP_ID_22959761,Human_RBP_ID_24544781,Human_RBP_ID_26331277,Human_RBP_ID_27812288 Human_Splice_Rec_1777428,Human_Splice_Rec_1777508,Human_Splice_Rec_1777590 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_182041,RMVar_hsa_circ_97071,RMVar_hsa_circ_364037,RMVar_hsa_circ_24589,RMVar_hsa_circ_26983,RMVar_hsa_circ_119481,RMVar_hsa_circ_182043,RMVar_hsa_circ_105459,RMVar_hsa_circ_70840,RMVar_hsa_circ_115357,RMVar_hsa_circ_182044,RMVar_hsa_circ_182045,RMVar_hsa_circ_377434,RMVar_hsa_circ_58748,RMVar_hsa_circ_20455,RMVar_hsa_circ_62004,RMVar_hsa_circ_182047,RMVar_hsa_circ_100349,RMVar_hsa_circ_285210,RMVar_hsa_circ_182046,RMVar_hsa_circ_274578,RMVar_hsa_circ_30677,RMVar_hsa_circ_182048,RMVar_hsa_circ_182049,RMVar_hsa_circ_83372,RMVar_hsa_circ_182050 104614 RMVar_ID_104614 Human_SNP_ID_616725300 m1A Human chr17 - 8513590 8513590 8513590 CAAAGATGAAGAGCTGTTGAAGGTGAAGGAGAAGCAGACGAAGGTGGAAGGAGAGCTGGAGGAGA CAAAGATGAAGAGCTGTTGAAGGTGAAGGAGAGGCAGACGAAGGTGGAAGGAGAGCTGGAGGAGA T C MYH10 Ensembl:ENSG00000133026 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:8513497..8513629;chr17:8513498..8513650;chr17:8513490..8513607 26863196 MeRIP-seq:(Medium) rs772155329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48055,Human_RBP_ID_1066803,Human_RBP_ID_1872068,Human_RBP_ID_4481916,Human_RBP_ID_5525335,Human_RBP_ID_24544785,Human_RBP_ID_26331280 Human_Splice_Rec_1777424,Human_Splice_Rec_1777425,Human_Splice_Rec_1777504,Human_Splice_Rec_1777505,Human_Splice_Rec_1777586,Human_Splice_Rec_1777587 RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_24589,RMVar_hsa_circ_119481,RMVar_hsa_circ_182043,RMVar_hsa_circ_105459,RMVar_hsa_circ_70840,RMVar_hsa_circ_115357,RMVar_hsa_circ_182044,RMVar_hsa_circ_182045,RMVar_hsa_circ_58748,RMVar_hsa_circ_62004,RMVar_hsa_circ_182047,RMVar_hsa_circ_100349,RMVar_hsa_circ_30677,RMVar_hsa_circ_35472,RMVar_hsa_circ_182049,RMVar_hsa_circ_83372,RMVar_hsa_circ_182050,RMVar_hsa_circ_22828,RMVar_hsa_circ_182051,RMVar_hsa_circ_110346 104615 RMVar_ID_104615 Human_SNP_ID_616726384 m1A Human chr17 - 8517706 8517706 8517706 TCAAGGCCGCCTGGCTGCGGTAGGCAGAATCCATTGAGAATTGGCCAAGAATAGAATTGGGAGGG TCAAGGCCGCCTGGCTGCGGTAGGCAGAATCCGTTGAGAATTGGCCAAGAATAGAATTGGGAGGG T C MYH10 Ensembl:ENSG00000133026 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8517667..8517895 26863196 MeRIP-seq:(Medium) rs922229283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20474,RMVar_hsa_circ_82056,RMVar_hsa_circ_84961,RMVar_hsa_circ_182037,RMVar_hsa_circ_26122,RMVar_hsa_circ_182038,RMVar_hsa_circ_24589,RMVar_hsa_circ_119481,RMVar_hsa_circ_182043,RMVar_hsa_circ_105459,RMVar_hsa_circ_115357,RMVar_hsa_circ_182044,RMVar_hsa_circ_182045,RMVar_hsa_circ_58748,RMVar_hsa_circ_62004,RMVar_hsa_circ_182047,RMVar_hsa_circ_100349,RMVar_hsa_circ_35472,RMVar_hsa_circ_182049,RMVar_hsa_circ_83372,RMVar_hsa_circ_182050,RMVar_hsa_circ_19390,RMVar_hsa_circ_182051,RMVar_hsa_circ_110346,RMVar_hsa_circ_50485 104616 RMVar_ID_104616 Human_SNP_ID_616742565 m1A Human chr17 - 8587607 8587607 8587607 GTGCAGAGCACAGGGGTTGGGTGTCTGGGCACAGTGAGGTCCTAGTGGGGGGCGCGACTCTTCTC GTGCAGAGCACAGGGGTTGGGTGTCTGGGCACGGTGAGGTCCTAGTGGGGGGCGCGACTCTTCTC T C MYH10 Ensembl:ENSG00000133026 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:8587559..8587733 26863196 MeRIP-seq:(Medium) rs1346550651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115357,RMVar_hsa_circ_182045,RMVar_hsa_circ_99189,RMVar_hsa_circ_182067,RMVar_hsa_circ_182072,RMVar_hsa_circ_79419,RMVar_hsa_circ_320651,RMVar_hsa_circ_338686,RMVar_hsa_circ_182080 104617 RMVar_ID_104617 Human_SNP_ID_616752371 m1A Human chr17 + 8629574 8629574 8629574 CAGGGCCGCATCCGCCCACCACAGGCCCACAAAGCCCCCACAAATGCCAGGACTCCGCGGCTTCA CAGGGCCGCATCCGCCCACCACAGGCCCACAACGCCCCCACAAATGCCAGGACTCCGCGGCTTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:8629572..8630266 26863196 MeRIP-seq:(Medium) rs1168410892 Functional Loss SNV dbSNP153 33..33 33 - - - 104618 RMVar_ID_104618 Human_SNP_ID_616752431 m1A Human chr17 + 8629780 8629780 8629780 CCCCCGGCCGTCCTGCTGCAGCGCGCCCCGCCACATTTCCCGCCTCGCCCCCTCAAACCGCCTGG CCCCCGGCCGTCCTGCTGCAGCGCGCCCCGCCGCATTTCCCGCCTCGCCCCCTCAAACCGCCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8629777..8629848 26863196 MeRIP-seq:(Medium) rs1438544425 Functional Loss SNV dbSNP153 33..33 33 - - - 104619 RMVar_ID_104619 Human_SNP_ID_616752433 m1A Human chr17 - 8629792 8629792 8629792 GCCCTGCGAGGCCCAGGCGGTTTGAGGGGGCGAGGCGGGAAATGTGGCGGGGCGCGCTGCAGCAG GCCCTGCGAGGCCCAGGCGGTTTGAGGGGGCGGGGCGGGAAATGTGGCGGGGCGCGCTGCAGCAG T C MYH10 Ensembl:ENSG00000133026 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:8629789..8629915 26863196 MeRIP-seq:(Medium) rs1194937264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542649 RMVar_hsa_circ_115357,RMVar_hsa_circ_182045 104620 RMVar_ID_104620 Human_SNP_ID_616909907 m1A Human chr17 - 9240210 9240210 9240210 CCCGTGAGGTAGCTACGTCTCGTCATTTCTCCAGGGCCCGGCCGGCGGCGCACCCCGCCCCGCGT CCCGTGAGGTAGCTACGTCTCGTCATTTCTCCTGGGCCCGGCCGGCGGCGCACCCCGCCCCGCGT T A lnc-STX8-4,lnc-STX8-4:2 RNACentral:URS00009BA8DC,RNACentral:URS00008B5588 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:9240159..9240240 26863196 MeRIP-seq:(Medium) rs539444778 Functional Loss SNV dbSNP153 33..33 33 - - - 104621 RMVar_ID_104621 Human_SNP_ID_616910690 m1A Human chr17 - 9242735 9242735 9242735 GGGTGTGTGGATAGGAAAGGCAGCTCGTGACGACCGTGCAATCCCAACAGTGACCTGGCTGCTAG GGGTGTGTGGATAGGAAAGGCAGCTCGTGACGCCCGTGCAATCCCAACAGTGACCTGGCTGCTAG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:9242661..9242748 26863410 MeRIP-seq:(Medium) rs1458156368 Functional Loss SNV dbSNP153 33..33 33 - - - 104622 RMVar_ID_104622 Human_SNP_ID_616910698 m1A Human chr17 - 9242746 9242746 9242746 GGGTCCTGGCTGGGTGTGTGGATAGGAAAGGCAGCTCGTGACGACCGTGCAATCCCAACAGTGAC GGGTCCTGGCTGGGTGTGTGGATAGGAAAGGCGGCTCGTGACGACCGTGCAATCCCAACAGTGAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:9242651..9242754 26863410 MeRIP-seq:(Medium) rs1209266026 Functional Loss SNV dbSNP153 33..33 33 - - - 104623 RMVar_ID_104623 Human_SNP_ID_616956157 m1A Human chr17 - 9413897 9413897 9413897 GTGGATGGACGGTTAGATGGACGGATGGATGGATGGATCGATGGATGGATCGATAGATGCATACA GTGGATGGACGGTTAGATGGACGGATGGATGGGTGGATCGATGGATGGATCGATAGATGCATACA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:9413887..9414052 26863196 MeRIP-seq:(Medium) rs528569384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648416,Human_RBP_ID_8189361 RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_97691,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_182091,RMVar_hsa_circ_35158,RMVar_hsa_circ_368338 104624 RMVar_ID_104624 Human_SNP_ID_616977418 m1A Human chr17 + 9491014 9491014 9491014 CTTTCCATAAATGCCAGCTTCACTGCCACTCAACGACTCCACGCTGTCACACGTCACCTCTACAC CTTTCCATAAATGCCAGCTTCACTGCCACTCAGCGACTCCACGCTGTCACACGTCACCTCTACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:9491004..9491235 26863196 MeRIP-seq:(Medium) rs1384037130 Functional Loss SNV dbSNP153 33..33 33 - - - 104625 RMVar_ID_104625 Human_SNP_ID_616999349 m1A Human chr17 + 9575700 9575700 9575700 TCTCGCTGCCCCTCCCCTCATCCCGAAAGGCCACCAGCGGCAATGCGAAGTGATTGCCTGCTCTC TCTCGCTGCCCCTCCCCTCATCCCGAAAGGCCGCCAGCGGCAATGCGAAGTGATTGCCTGCTCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:9575690..9575770 26863196 MeRIP-seq:(Medium) rs112179867 Functional Loss SNV dbSNP153 33..33 33 - - - 104626 RMVar_ID_104626 Human_SNP_ID_616999357 m1A Human chr17 - 9575731 9575731 9575731 TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGAGAGCAGGCAATCACTTCGCATTGCCGCTGGTG TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGTGAGCAGGCAATCACTTCGCATTGCCGCTGGTG T A STX8 Ensembl:ENSG00000170310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:9575716..9575805 26863196 MeRIP-seq:(Medium) rs7210038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_182093 104627 RMVar_ID_104627 Human_SNP_ID_616999358 m1A Human chr17 - 9575731 9575731 9575731 TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGAGAGCAGGCAATCACTTCGCATTGCCGCTGGTG TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGGGAGCAGGCAATCACTTCGCATTGCCGCTGGTG T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:9575716..9575805 26863196 MeRIP-seq:(Medium) rs7210038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_182093 104628 RMVar_ID_104628 Human_SNP_ID_617291083 m1A Human chr17 + 10695700 10695699 10695701 AACAACAAAAAAGGTGCTAGTCCATAGCCAGGAAGACCTTTATACAGGGCTGAGCAGATGATAAT AACAACAAAAAAGGTGCTAGTCCATAGCCAGG__GACCTTTATACAGGGCTGAGCAGATGATAAT GAA G lnc-ADPRM-6 RNACentral:URS0000D5D6C5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:10695696..10695771 26863196 MeRIP-seq:(Medium) rs199665575 Functional Loss DEL dbSNP153 33..34 33 - - - 104629 RMVar_ID_104629 Human_SNP_ID_617291656 m1A Human chr17 - 10697275 10697275 10697275 CAGCACTGCGAGGCCGCCACCCCCGTGGTCGCAGAAGGGCCCCGGAGACTCCACGCGCCCCTCGA CAGCACTGCGAGGCCGCCACCCCCGTGGTCGCCGAAGGGCCCCGGAGACTCCACGCGCCCCTCGA T G SCO1 Ensembl:ENSG00000133028 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:10697226..10697489 26863410 MeRIP-seq:(Medium) rs1342846995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236224,Human_RBP_ID_899423,Human_RBP_ID_22443465 Human_Splice_Rec_1779843,Human_Splice_Rec_1779853,Human_Splice_Rec_1779865,Human_Splice_Rec_1779879 RMVar_hsa_circ_88303,RMVar_hsa_circ_182123 104630 RMVar_ID_104630 Human_SNP_ID_617622410 m1A Human chr17 + 11997047 11997045 11997047 TGCGCCCCCCAAATGCCGACTGCACTCTGATGAGAGAGGGAGAGACTCCAGGCATCATCCCATCG TGCGCCCCCCAAATGCCGACTGCACTCTGAT__GAGAGGGAGAGACTCCAGGCATCATCCCATCG TGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:11997018..11997106 32194978 MeRIP-seq:(Medium) rs886817745 Functional Loss DEL dbSNP153 32..33 33 - - - 104631 RMVar_ID_104631 Human_SNP_ID_617664032 m1A Human chr17 - 12167929 12167902 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG____________________________AAGGAC TCCTTCCTTCCTTCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs1430009376 Functional Loss DEL dbSNP153 32..59 33 - - - 104632 RMVar_ID_104632 Human_SNP_ID_617664036 m1A Human chr17 - 12167929 12167906 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG________________________AAGGAAGGAC TCCTTCCTTCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs796247216 Functional Loss DEL dbSNP153 32..55 33 - - - 104633 RMVar_ID_104633 Human_SNP_ID_617664042 m1A Human chr17 - 12167929 12167907 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG_______________________GAAGGAAGGAC CCTTCCTTCCTTCCTGCCTTCCTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs1355573651 Functional Loss DEL dbSNP153 32..54 33 - - - 104634 RMVar_ID_104634 Human_SNP_ID_617664045 m1A Human chr17 - 12167929 12167910 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG____________________AAGGAAGGAAGGAC TCCTTCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs1230996621 Functional Loss DEL dbSNP153 32..51 33 - - - 104635 RMVar_ID_104635 Human_SNP_ID_617664050 m1A Human chr17 - 12167929 12167914 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG________________AAGGAAGGAAGGAAGGAC TCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs746281811 Functional Loss DEL dbSNP153 32..47 33 - - - 104636 RMVar_ID_104636 Human_SNP_ID_617664051 m1A Human chr17 - 12167929 12167914 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG________CAGGAAGGAAGGAAGGAAGGAAGGAC TCCTTCCTGCCTTCCTG TCCTTCCTG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs746281811 Functional Loss DEL dbSNP153 32..39 33 - - - 104637 RMVar_ID_104637 Human_SNP_ID_617664055 m1A Human chr17 - 12167929 12167918 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG____________AAGGAAGGAAGGAAGGAAGGAC TCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs1454971332 Functional Loss DEL dbSNP153 32..43 33 - - - 104638 RMVar_ID_104638 Human_SNP_ID_617664065 m1A Human chr17 - 12167929 12167925 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG_____AGGCAGGAAGGAAGGAAGGAAGGAAGGAC TTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs1310147385 Functional Loss DEL dbSNP153 32..36 33 - - - 104639 RMVar_ID_104639 Human_SNP_ID_617664066 m1A Human chr17 - 12167929 12167926 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG____AAGGCAGGAAGGAAGGAAGGAAGGAAGGAC TCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs200103184 Functional Loss DEL dbSNP153 32..35 33 - - - 104640 RMVar_ID_104640 Human_SNP_ID_617821173 m1A Human chr17 + 12789716 12789716 12789716 AGGGAGCTGCGCGCGGGCCAGACGGCGCCCGGAGGCTCCGCAGTGCCGCCGCCGTCGCCCGGGAG AGGGAGCTGCGCGCGGGCCAGACGGCGCCCGGTGGCTCCGCAGTGCCGCCGCCGTCGCCCGGGAG A T ARHGAP44 Ensembl:ENSG00000006740 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:12789549..12789733 26863410 MeRIP-seq:(Medium) rs1269836377 Functional Loss SNV dbSNP153 33..33 33 - - - 104641 RMVar_ID_104641 Human_SNP_ID_617867208 m1A Human chr17 - 12974206 12974206 12974206 GGCTGCTCCGGCAGCGGCGAAGGCAGGGGCGCAGCCAGCTCGGCGGGCGGGGCGGGAGGCTGCAT GGCTGCTCCGGCAGCGGCGAAGGCAGGGGCGCCGCCAGCTCGGCGGGCGGGGCGGGAGGCTGCAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:12974157..12974236 26863196 MeRIP-seq:(Medium) rs1443242776 Functional Loss SNV dbSNP153 33..33 33 - - - 104642 RMVar_ID_104642 Human_SNP_ID_617873259 m1A Human chr17 - 12992899 12992899 12992899 GTGCGGGCGGCCCTCCTGTCCAGGGAGCTGGCAGGCGGCCTGGAGGATGGGGAGCCTCAGCAGAA GTGCGGGCGGCCCTCCTGTCCAGGGAGCTGGCGGGCGGCCTGGAGGATGGGGAGCCTCAGCAGAA T C ELAC2 Ensembl:ENSG00000006744 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:12992797..12992950 26863410 MeRIP-seq:(Medium) rs748616092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50199,Human_RBP_ID_237448,Human_RBP_ID_4405693,Human_RBP_ID_5318271,Human_RBP_ID_6559083,Human_RBP_ID_9375397,Human_RBP_ID_22443466 104643 RMVar_ID_104643 Human_SNP_ID_617877233 m1A Human chr17 - 13005417 13005417 13005417 GGCCTGGGGTTTATGGTCCAGAGGAATGCCACAGTATTCTATGTCAAGATATTTCCTCTGACTTC GGCCTGGGGTTTATGGTCCAGAGGAATGCCACTGTATTCTATGTCAAGATATTTCCTCTGACTTC T A ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4792310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21975404 GWAS_ID_13696 RMVar_hsa_circ_76884,RMVar_hsa_circ_182179,RMVar_hsa_circ_99844,RMVar_hsa_circ_63049,RMVar_hsa_circ_110157,RMVar_hsa_circ_182180,RMVar_hsa_circ_372822,RMVar_hsa_circ_182181,RMVar_hsa_circ_23609,RMVar_hsa_circ_182183 104644 RMVar_ID_104644 Human_SNP_ID_617877234 m1A Human chr17 - 13005417 13005417 13005417 GGCCTGGGGTTTATGGTCCAGAGGAATGCCACAGTATTCTATGTCAAGATATTTCCTCTGACTTC GGCCTGGGGTTTATGGTCCAGAGGAATGCCACGGTATTCTATGTCAAGATATTTCCTCTGACTTC T C ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4792310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21975404 GWAS_ID_13696 RMVar_hsa_circ_76884,RMVar_hsa_circ_182179,RMVar_hsa_circ_99844,RMVar_hsa_circ_63049,RMVar_hsa_circ_110157,RMVar_hsa_circ_182180,RMVar_hsa_circ_372822,RMVar_hsa_circ_182181,RMVar_hsa_circ_23609,RMVar_hsa_circ_182183 104645 RMVar_ID_104645 Human_SNP_ID_617881234 m1A Human chr17 + 13017960 13017960 13017960 AGCGAGCAAAGCGCCCACATGCGCCCGTCTCCACCAAAACTGAGAAAGCCGCCGGTCACCTACGC AGCGAGCAAAGCGCCCACATGCGCCCGTCTCCCCCAAAACTGAGAAAGCCGCCGGTCACCTACGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:13017763..13018025 26863196 MeRIP-seq:(Medium) rs1024497303 Functional Loss SNV dbSNP153 33..33 33 - - - 104646 RMVar_ID_104646 Human_SNP_ID_617881235 m1A Human chr17 + 13017960 13017960 13017960 AGCGAGCAAAGCGCCCACATGCGCCCGTCTCCACCAAAACTGAGAAAGCCGCCGGTCACCTACGC AGCGAGCAAAGCGCCCACATGCGCCCGTCTCCGCCAAAACTGAGAAAGCCGCCGGTCACCTACGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:13017763..13018025 26863196 MeRIP-seq:(Medium) rs1024497303 Functional Loss SNV dbSNP153 33..33 33 - - - 104647 RMVar_ID_104647 Human_SNP_ID_617968775 m1A Human chr17 + 13347676 13347676 13347676 GAGCAGGAAATCAGAATGAGTCAGGGTGGAGAATGAGTCAGGGCAGAGCAGGGAATTGGAATGAG GAGCAGGAAATCAGAATGAGTCAGGGTGGAGACTGAGTCAGGGCAGAGCAGGGAATTGGAATGAG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:13347670..13347757 26863410 MeRIP-seq:(Medium) rs1001955506 Functional Loss SNV dbSNP153 33..33 33 - - - 104648 RMVar_ID_104648 Human_SNP_ID_618037385 m1A Human chr17 - 13601683 13601683 13601683 CTCCTTGGCTGAGAGAACCTGAACTCGGGCGGAGAGAACGCGCCCAGGCGGGCAAGGGGACCAGA CTCCTTGGCTGAGAGAACCTGAACTCGGGCGGCGAGAACGCGCCCAGGCGGGCAAGGGGACCAGA T G HS3ST3A1 Ensembl:ENSG00000153976 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:13601542..13601921 26863196 MeRIP-seq:(Medium) rs1429870877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5184975 RMVar_hsa_circ_269444 104649 RMVar_ID_104649 Human_SNP_ID_618037433 m1A Human chr17 - 13601840 13601836 13601841 GCTGACAGGTCCCGCGCAGCCCAGCCCAGCCCAGCCACGCGGCTCACAGGTGGGGTCCAAGAGCA GCTGACAGGTCCCGCGCAGCCCAGCCCAGCC_____ACGCGGCTCACAGGTGGGGTCCAAGAGCA TGGCTG T HS3ST3A1 Ensembl:ENSG00000153976 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:13601792..13601917 26863196 MeRIP-seq:(Medium) rs1411259889 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_4465169,Human_RBP_ID_22208947 RMVar_hsa_circ_269444 104650 RMVar_ID_104650 Human_SNP_ID_618158250 m1A Human chr17 + 14069362 14069362 14069362 GTCCGCGCGCGGCTTTTTCTTCAGGACAGCGGAGGCACACCGTGCTTTGCGGTTCCCGGAAGTCC GTCCGCGCGCGGCTTTTTCTTCAGGACAGCGGCGGCACACCGTGCTTTGCGGTTCCCGGAAGTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:14069312..14069450 26863196 MeRIP-seq:(Medium) rs1173608233 Functional Loss SNV dbSNP153 33..33 33 - - - 104651 RMVar_ID_104651 Human_SNP_ID_618158348 m1A Human chr17 + 14069562 14069562 14069562 GAAGATGGCGGCGCCCAGCGTCCCGTGAGGAGAGAGGACACAGGGATCCCGGGGAGCGGCCCCAG GAAGATGGCGGCGCCCAGCGTCCCGTGAGGAGCGAGGACACAGGGATCCCGGGGAGCGGCCCCAG A C COX10 Ensembl:ENSG00000006695 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:14069511..14069600 26863196 MeRIP-seq:(Medium) rs758320502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144049,Human_RBP_ID_6560476,Human_RBP_ID_17885388,Human_RBP_ID_18419881 Human_Splice_Rec_1781645,Human_Splice_Rec_1781663,Human_Splice_Rec_1781687,Human_Splice_Rec_1781691,Human_Splice_Rec_1781703,Human_Splice_Rec_1781713 Human_miRNA_ID_2571219,Human_miRNA_ID_3044956 RMVar_hsa_circ_182196,RMVar_hsa_circ_126750 104652 RMVar_ID_104652 Human_SNP_ID_618158349 m1A Human chr17 + 14069562 14069562 14069562 GAAGATGGCGGCGCCCAGCGTCCCGTGAGGAGAGAGGACACAGGGATCCCGGGGAGCGGCCCCAG GAAGATGGCGGCGCCCAGCGTCCCGTGAGGAGGGAGGACACAGGGATCCCGGGGAGCGGCCCCAG A G COX10 Ensembl:ENSG00000006695 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:14069511..14069600 26863196 MeRIP-seq:(Medium) rs758320502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144049,Human_RBP_ID_6560476,Human_RBP_ID_17885388,Human_RBP_ID_18419881 Human_Splice_Rec_1781645,Human_Splice_Rec_1781663,Human_Splice_Rec_1781687,Human_Splice_Rec_1781691,Human_Splice_Rec_1781703,Human_Splice_Rec_1781713 Human_miRNA_ID_2571219,Human_miRNA_ID_3044956 RMVar_hsa_circ_182196,RMVar_hsa_circ_126750 104653 RMVar_ID_104653 Human_SNP_ID_618161320 m1A Human chr17 - 14081960 14081960 14081960 CTCTCCACCTGGATATGCCAGTAGCAACTCAAATTCCACTTATCCAAAATTGAACTCATCATGTT CTCTCCACCTGGATATGCCAGTAGCAACTCAAGTTCCACTTATCCAAAATTGAACTCATCATGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:14081937..14082222 26863196 MeRIP-seq:(Medium) rs1033622922 Functional Loss SNV dbSNP153 33..33 33 - - - 104654 RMVar_ID_104654 Human_SNP_ID_618190663 m1A Human chr17 + 14212943 14212943 14212943 GCAGGGTGAGCAAAGGCCCAGGGTGAAGGGGCATCGAGTGTTTGGGGAGCATTCGCAGTTCTGCA GCAGGGTGAGCAAAGGCCCAGGGTGAAGGGGCTTCGAGTGTTTGGGGAGCATTCGCAGTTCTGCA A T COX10 Ensembl:ENSG00000006695 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:14212893..14212986 26863196 MeRIP-seq:(Medium) rs1338137073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18438373 RMVar_hsa_circ_182202 104655 RMVar_ID_104655 Human_SNP_ID_618190679 m1A Human chr17 - 14213017 14213017 14213017 TGGCCAGACCTGGTCCCTCCGCTTCTGTCTTCAACGTCATCCTCCAGCTCTTCCTGGCCCCTACC TGGCCAGACCTGGTCCCTCCGCTTCTGTCTTCGACGTCATCCTCCAGCTCTTCCTGGCCCCTACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:14212950..14213046 26863196 MeRIP-seq:(Medium) rs574828144 Functional Loss SNV dbSNP153 33..33 33 - - - 104656 RMVar_ID_104656 Human_SNP_ID_618190680 m1A Human chr17 - 14213017 14213017 14213017 TGGCCAGACCTGGTCCCTCCGCTTCTGTCTTCAACGTCATCCTCCAGCTCTTCCTGGCCCCTACC TGGCCAGACCTGGTCCCTCCGCTTCTGTCTTCCACGTCATCCTCCAGCTCTTCCTGGCCCCTACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:14212950..14213046 26863196 MeRIP-seq:(Medium) rs574828144 Functional Loss SNV dbSNP153 33..33 33 - - - 104657 RMVar_ID_104657 Human_SNP_ID_618321058 m1A Human chr17 - 14705403 14705403 14705403 AAGGGTGTGGGCCGAAGATATGCTCATGTGGTATTGAGGAAAGCAGACATTGACCTCACCAAGAG AAGGGTGTGGGCCGAAGATATGCTCATGTGGTGTTGAGGAAAGCAGACATTGACCTCACCAAGAG T C RPS18P12 Ensembl:ENSG00000230897 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879089855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1901607,Human_miRNA_ID_1903085 104658 RMVar_ID_104658 Human_SNP_ID_618321077 m1A Human chr17 + 14705465 14705465 14705465 CTTAATGGCAGTGATGGCAAAGGCTATTTTCCACCGCCCATCGATGTTGGTGTTGAGTACTCGCA CTTAATGGCAGTGATGGCAAAGGCTATTTTCCGCCGCCCATCGATGTTGGTGTTGAGTACTCGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:14705385..14705467 32194978 MeRIP-seq:(Medium) rs878960552 Functional Loss SNV dbSNP153 33..33 33 - - - 104659 RMVar_ID_104659 Human_SNP_ID_618321099 m1A Human chr17 + 14705533 14705533 14705533 TATGCTGGAACTTTTCAGGGATCACTAGAGACATGGCAGCAGCACAAGCGGCGGCGTGTAGGCCT TATGCTGGAACTTTTCAGGGATCACTAGAGACGTGGCAGCAGCACAAGCGGCGGCGTGTAGGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:14705454..14705537 26863196 MeRIP-seq:(Medium) rs1051477080 Functional Loss SNV dbSNP153 33..33 33 - - - 104660 RMVar_ID_104660 Human_SNP_ID_461033987 m1A Human chr11 - 31369886 31369886 31369886 ACCTACCTAACTTCACATAGGCGCTGCTACCCACTCCTCGCCTGCTGTCGGCCAGAACTCCGGAC ACCTACCTAACTTCACATAGGCGCTGCTACCCGCTCCTCGCCTGCTGTCGGCCAGAACTCCGGAC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr11:31369857..31369983;chr11:31369863..31369995;chr11:31369856..31369985 26863196 MeRIP-seq:(Medium) rs1032135147 Functional Loss SNV dbSNP153 33..33 33 - - - 104661 RMVar_ID_104661 Human_SNP_ID_461033994 m1A Human chr11 + 31369901 31369901 31369901 CGACAGCAGGCGAGGAGTGGGTAGCAGCGCCTATGTGAAGTTAGGTAGGTCTGATGTCGTATAAA CGACAGCAGGCGAGGAGTGGGTAGCAGCGCCTCTGTGAAGTTAGGTAGGTCTGATGTCGTATAAA A C DNAJC24 Ensembl:ENSG00000170946 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:31369850..31369980 26863196 MeRIP-seq:(Medium) rs1442820629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416535 Human_Splice_Rec_1223491,Human_Splice_Rec_1223495,Human_Splice_Rec_1223499,Human_Splice_Rec_1223505,Human_Splice_Rec_1223511,Human_Splice_Rec_1223519,Human_Splice_Rec_1223527 104662 RMVar_ID_104662 Human_SNP_ID_461033995 m1A Human chr11 + 31369901 31369901 31369901 CGACAGCAGGCGAGGAGTGGGTAGCAGCGCCTATGTGAAGTTAGGTAGGTCTGATGTCGTATAAA CGACAGCAGGCGAGGAGTGGGTAGCAGCGCCTTTGTGAAGTTAGGTAGGTCTGATGTCGTATAAA A T DNAJC24 Ensembl:ENSG00000170946 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:31369850..31369980 26863196 MeRIP-seq:(Medium) rs1442820629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18416535 Human_Splice_Rec_1223491,Human_Splice_Rec_1223495,Human_Splice_Rec_1223499,Human_Splice_Rec_1223505,Human_Splice_Rec_1223511,Human_Splice_Rec_1223519,Human_Splice_Rec_1223527 104663 RMVar_ID_104663 Human_SNP_ID_461034188 m1A Human chr11 - 31370662 31370662 31370662 AATTCATCACAGTTTGCCATGTATCTAAGAAAAAATTAAGTACTGCCCTTGTAAATTCTTTAGTA AATTCATCACAGTTTGCCATGTATCTAAGAAAGAATTAAGTACTGCCCTTGTAAATTCTTTAGTA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:31370660..31370800 26863196 MeRIP-seq:(Medium) rs1024453070 Functional Loss SNV dbSNP153 33..33 33 - - - 104664 RMVar_ID_104664 Human_SNP_ID_461066234 m1A Human chr11 - 31509826 31509826 31509826 TTGCTCTTGCTGGCTGTCGCCACTGCAGACCCAGTACTCGCGGCAACACTACCGCAGGTTGCCAC TTGCTCTTGCTGGCTGTCGCCACTGCAGACCCCGTACTCGCGGCAACACTACCGCAGGTTGCCAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:31509776..31509911 26863196 MeRIP-seq:(Medium) rs1197413232 Functional Loss SNV dbSNP153 33..33 33 - - - 104665 RMVar_ID_104665 Human_SNP_ID_461212851 m1A Human chr11 - 32091166 32091166 32091166 ATCGTCCCGAGGAGAGGGCGGCCGAGAGGGAGACGCTGAGCGAGCGACAACAGCGGCAGCTCGGG ATCGTCCCGAGGAGAGGGCGGCCGAGAGGGAGTCGCTGAGCGAGCGACAACAGCGGCAGCTCGGG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:32090990..32091382 26863410 MeRIP-seq:(Medium) rs563525926 Functional Loss SNV dbSNP153 33..33 33 - - - 104666 RMVar_ID_104666 Human_SNP_ID_461212882 m1A Human chr11 - 32091237 32091237 32091237 GCGGCGCCAGCACCAGCGCCAGCAGCAGCCCCAGGGCTAACCCCAGGCGGCGGCCGCGGCCACCG GCGGCGCCAGCACCAGCGCCAGCAGCAGCCCCGGGGCTAACCCCAGGCGGCGGCCGCGGCCACCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:32091067..32091336 26863196 MeRIP-seq:(Medium) rs1255286560 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 104667 RMVar_ID_104667 Human_SNP_ID_461212977 m1A Human chr11 - 32091401 32091401 32091401 CTCGTCCGGGGTGAGCTGGTCGAAGGTCTTGGAGTCCTCCTTGCCCAGGAAGGCCTCGTGGTCGT CTCGTCCGGGGTGAGCTGGTCGAAGGTCTTGGGGTCCTCCTTGCCCAGGAAGGCCTCGTGGTCGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr11:32091376..32091400 26863196,32194978 MeRIP-seq:(Medium) rs1423439187 Functional Loss SNV dbSNP153 33..33 33 - - - 104668 RMVar_ID_104668 Human_SNP_ID_461213588 m1A Human chr11 + 32093706 32093705 32093707 TGAGAGGTGAGAATGGAGGGGAAACCAAGGGCAGAGCAGGAAGGACCTTGGTGAGATGGACATGA TGAGAGGTGAGAATGGAGGGGAAACCAAGGGC__AGCAGGAAGGACCTTGGTGAGATGGACATGA CAG C RCN1,AL035078.4 Ensembl:ENSG00000049449,Ensembl:ENSG00000285283 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:32093431..32093948 26863196 MeRIP-seq:(Medium) rs765087913 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6067771 104669 RMVar_ID_104669 Human_SNP_ID_461335548 m1A Human chr11 - 32583931 32583930 32583931 CCCACCGTGGCGGCACCCGTAGACCGAAGCACACCTGATCTTCTTCACTGATGTCGATGAAGGCC CCCACCGTGGCGGCACCCGTAGACCGAAGCAC_CCTGATCTTCTTCACTGATGTCGATGAAGGCC GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:32583911..32584012 32194978 MeRIP-seq:(Medium) rs775102870 Functional Loss DEL dbSNP153 33..33 33 - - - 104670 RMVar_ID_104670 Human_SNP_ID_461335550 m1A Human chr11 - 32583931 32583931 32583931 CCCACCGTGGCGGCACCCGTAGACCGAAGCACACCTGATCTTCTTCACTGATGTCGATGAAGGCC CCCACCGTGGCGGCACCCGTAGACCGAAGCACGCCTGATCTTCTTCACTGATGTCGATGAAGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:32583911..32584012 32194978 MeRIP-seq:(Medium) rs111796827 Functional Loss SNV dbSNP153 33..33 33 - - - 104671 RMVar_ID_104671 Human_SNP_ID_461397962 m1A Human chr11 + 32853895 32853889 32853895 AAGAAAAGAGAAGAAGGAGAAGGAGATGAAGGAGGAGGAGGAGGAGAAGGAGAAGAAGAAGAAGA AAGAAAAGAGAAGAAGGAGAAGGAGAT______GGAGGAGGAGGAGAAGGAGAAGAAGAAGAAGA TGAAGGA T PRRG4 Ensembl:ENSG00000135378 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:32853845..32853956 26863196 MeRIP-seq:(Medium) rs1178530435 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_117764,RMVar_hsa_circ_115469,RMVar_hsa_circ_148870,RMVar_hsa_circ_86171,RMVar_hsa_circ_148871,RMVar_hsa_circ_148872 104672 RMVar_ID_104672 Human_SNP_ID_461397973 m1A Human chr11 + 32853901 32853901 32853901 AGAGAAGAAGGAGAAGGAGATGAAGGAGGAGGAGGAGGAGAAGGAGAAGAAGAAGAAGAAGAAGA AGAGAAGAAGGAGAAGGAGATGAAGGAGGAGGCGGAGGAGAAGGAGAAGAAGAAGAAGAAGAAGA A C PRRG4 Ensembl:ENSG00000135378 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:32853853..32853943 26863196 MeRIP-seq:(Medium) rs1244389843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117764,RMVar_hsa_circ_115469,RMVar_hsa_circ_148870,RMVar_hsa_circ_86171,RMVar_hsa_circ_148871,RMVar_hsa_circ_148872 104673 RMVar_ID_104673 Human_SNP_ID_461407683 m1A Human chr11 - 32893202 32893202 32893202 GGGCGGGGGGCTGCGCAGCGGCGCTGGCGGGGACGGGGGCGGCGGGGGGCGCGGGCGGCGGCGGC GGGCGGGGGGCTGCGCAGCGGCGCTGGCGGGGGCGGGGGCGGCGGGGGGCGCGGGCGGCGGCGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:32892956..32893237 26863196 MeRIP-seq:(Medium) rs991256704 Functional Loss SNV dbSNP153 33..33 33 - - - 104674 RMVar_ID_104674 Human_SNP_ID_461407863 m1A Human chr11 + 32893787 32893787 32893787 GGACTCCGGCGTGTGAGGGTTGCGGAGGCGGGAGAGGAAGAGTCGCGGAACCGCGTCCCGGAGAC GGACTCCGGCGTGTGAGGGTTGCGGAGGCGGGCGAGGAAGAGTCGCGGAACCGCGTCCCGGAGAC A C QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:32893425..32893968 26863196 MeRIP-seq:(Medium) rs1374374075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259697,Human_RBP_ID_751949,Human_RBP_ID_806989,Human_RBP_ID_3384084,Human_RBP_ID_5313575,Human_RBP_ID_8064147,Human_RBP_ID_8174163,Human_RBP_ID_8229064,Human_RBP_ID_8725195,Human_RBP_ID_17204893,Human_RBP_ID_17350502,Human_RBP_ID_18416802,Human_RBP_ID_18477639,Human_RBP_ID_21966010,Human_RBP_ID_22471749,Human_RBP_ID_26776224 104675 RMVar_ID_104675 Human_SNP_ID_461407867 m1A Human chr11 + 32893793 32893793 32893793 CGGCGTGTGAGGGTTGCGGAGGCGGGAGAGGAAGAGTCGCGGAACCGCGTCCCGGAGACACTGGG CGGCGTGTGAGGGTTGCGGAGGCGGGAGAGGAGGAGTCGCGGAACCGCGTCCCGGAGACACTGGG A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:32893787..32893890 26863196 MeRIP-seq:(Medium) rs1255690963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259697,Human_RBP_ID_751949,Human_RBP_ID_806989,Human_RBP_ID_3384084,Human_RBP_ID_5313575,Human_RBP_ID_8064147,Human_RBP_ID_8174163,Human_RBP_ID_8229064,Human_RBP_ID_8725195,Human_RBP_ID_9321353,Human_RBP_ID_17204893,Human_RBP_ID_17350502,Human_RBP_ID_18416802,Human_RBP_ID_18477639,Human_RBP_ID_21966010,Human_RBP_ID_22471749 104676 RMVar_ID_104676 Human_SNP_ID_461470078 m1A Human chr11 - 33161346 33161346 33161346 CTTTTCTAGCTTCCCATCGACGGTCAGTGCGCACGTTGTAATCAGCTGAGGCCATGTCAGGAGAC CTTTTCTAGCTTCCCATCGACGGTCAGTGCGCGCGTTGTAATCAGCTGAGGCCATGTCAGGAGAC T C CSTF3 Ensembl:ENSG00000176102 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:33161231..33161418 26863196 MeRIP-seq:(Medium) rs756084169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31644,Human_RBP_ID_807608,Human_RBP_ID_869426,Human_RBP_ID_4189970,Human_RBP_ID_6069319,Human_RBP_ID_11602763,Human_RBP_ID_18973420,Human_RBP_ID_22790262,Human_RBP_ID_22890401,Human_RBP_ID_23113167,Human_RBP_ID_23502470,Human_RBP_ID_24557035,Human_RBP_ID_24882438,Human_RBP_ID_26889877 Human_Splice_Rec_1226291,Human_Splice_Rec_1226331,Human_Splice_Rec_1226373,Human_Splice_Rec_1226381,Human_Splice_Rec_1226385,Human_Splice_Rec_1226387,Human_Splice_Rec_1226394,Human_Splice_Rec_1226395 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 104677 RMVar_ID_104677 Human_SNP_ID_461470094 m1A Human chr11 + 33161391 33161391 33161391 TCGATGGGAAGCTAGAAAAGAAAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCC TCGATGGGAAGCTAGAAAAGAAAAATTAAACTGAAAACCACCCCCAAATCAGTAAAGTTACCCCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:33161301..33161475 26863410 MeRIP-seq:(Medium) rs549893325 Functional Loss SNV dbSNP153 33..33 33 - - - 104678 RMVar_ID_104678 Human_SNP_ID_461470098 m1A Human chr11 + 33161412 33161411 33161413 AAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGC AAAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGC TAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:33161248..33161475;chr11:33161209..33161484;chr11:33156794..33161489 26863196 MeRIP-seq:(Medium) rs1408775438 Functional Loss DEL dbSNP153 33..34 33 - - - 104679 RMVar_ID_104679 Human_SNP_ID_461493831 m1A Human chr11 + 33257345 33257345 33257345 CGGTGGCGCTGCGGAGGCGGTGGCCGAGGCCGACGAGCGCGGAGGAGGGGCCCGAGGCTGGGGCG CGGTGGCGCTGCGGAGGCGGTGGCCGAGGCCGGCGAGCGCGGAGGAGGGGCCCGAGGCTGGGGCG A G HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:33257295..33257623 26863196 MeRIP-seq:(Medium) rs1364544960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4158241 104680 RMVar_ID_104680 Human_SNP_ID_461493834 m1A Human chr11 + 33257348 33257348 33257348 TGGCGCTGCGGAGGCGGTGGCCGAGGCCGACGAGCGCGGAGGAGGGGCCCGAGGCTGGGGCGGCT TGGCGCTGCGGAGGCGGTGGCCGAGGCCGACGGGCGCGGAGGAGGGGCCCGAGGCTGGGGCGGCT A G HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:33257300..33257413 26863196 MeRIP-seq:(Medium) rs1157387899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4158242 104681 RMVar_ID_104681 Human_SNP_ID_461493835 m1A Human chr11 + 33257348 33257348 33257348 TGGCGCTGCGGAGGCGGTGGCCGAGGCCGACGAGCGCGGAGGAGGGGCCCGAGGCTGGGGCGGCT TGGCGCTGCGGAGGCGGTGGCCGAGGCCGACGTGCGCGGAGGAGGGGCCCGAGGCTGGGGCGGCT A T HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:33257300..33257413 26863196 MeRIP-seq:(Medium) rs1157387899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4158242 104682 RMVar_ID_104682 Human_SNP_ID_461493846 m1A Human chr11 - 33257380 33257380 33257380 TGCCGGCAGTCGTCACTGAGGCAGCTGCCACCAGCCGCCCCAGCCTCGGGCCCCTCCTCCGCGCT TGCCGGCAGTCGTCACTGAGGCAGCTGCCACCCGCCGCCCCAGCCTCGGGCCCCTCCTCCGCGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:33257276..33257665 26863196 MeRIP-seq:(Medium) rs528654516 Functional Loss SNV dbSNP153 33..33 33 - - - 104683 RMVar_ID_104683 Human_SNP_ID_461518665 m1A Human chr11 + 33353366 33353366 33353366 CTCTCCGTGTACCTCAAGACCTATGTTACAGCATCCAACTTATAATATCTCCCATCCCAGTGGCA CTCTCCGTGTACCTCAAGACCTATGTTACAGCTTCCAACTTATAATATCTCCCATCCCAGTGGCA A T HIPK3 Ensembl:ENSG00000110422 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:33353226..33353500 26863196 MeRIP-seq:(Medium) rs1164175602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8061505,Human_RBP_ID_17233961,Human_RBP_ID_17348405,Human_RBP_ID_17464520,Human_RBP_ID_17795047,Human_RBP_ID_27617438 104684 RMVar_ID_104684 Human_SNP_ID_461606243 m1A Human chr11 - 33710119 33710119 33710119 CAGCAGCCTGGAGCCTTCATCCCTAAGTCAACACCAGGAGAGCTTCTCCCAAACTCCCCGTTCCT CAGCAGCCTGGAGCCTTCATCCCTAAGTCAACTCCAGGAGAGCTTCTCCCAAACTCCCCGTTCCT T A AL049629.2,CD59 Ensembl:ENSG00000284969,Ensembl:ENSG00000085063 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:33710069..33710312 26863196 MeRIP-seq:(Medium) rs1461882274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395341,Human_RBP_ID_751833,Human_RBP_ID_807079,Human_RBP_ID_1161852,Human_RBP_ID_4158512,Human_RBP_ID_5110374,Human_RBP_ID_8350288,Human_RBP_ID_17231996,Human_RBP_ID_17649038,Human_RBP_ID_22034356,Human_RBP_ID_22433457,Human_RBP_ID_22754629,Human_RBP_ID_23502766,Human_RBP_ID_24403145,Human_RBP_ID_24459713,Human_RBP_ID_27200980,Human_RBP_ID_27411148 RMVar_hsa_circ_71945,RMVar_hsa_circ_17880 104685 RMVar_ID_104685 Human_SNP_ID_461607984 m1A Human chr11 + 33717454 33717454 33717454 TTTGCAGTCAGCAGTTGGGTTAGGACAGTTGTAGCACTGCAGGCTATGACCTAGAATCAGGAAGA TTTGCAGTCAGCAGTTGGGTTAGGACAGTTGTCGCACTGCAGGCTATGACCTAGAATCAGGAAGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:33717351..33717526 32194978 MeRIP-seq:(Medium) rs1564972905 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_669 104686 RMVar_ID_104686 Human_SNP_ID_461609189 m1A Human chr11 - 33722451 33722451 33722451 TTCCTGTCCCTTCCTTCCAGGTTCTGTGGACAATCACAATGGGAATCCAAGGAGGGTCTGTCCTG TTCCTGTCCCTTCCTTCCAGGTTCTGTGGACAGTCACAATGGGAATCCAAGGAGGGTCTGTCCTG T C AL049629.2,CD59 Ensembl:ENSG00000284969,Ensembl:ENSG00000085063 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr11:33722333..33722496;chr11:33722426..33722475 26863196 MeRIP-seq:(Medium) rs778710215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29553,Human_RBP_ID_749034,Human_RBP_ID_806702,Human_RBP_ID_986917,Human_RBP_ID_4184742,Human_RBP_ID_5313578,Human_RBP_ID_9321357,Human_RBP_ID_17649506,Human_RBP_ID_22434266,Human_RBP_ID_22641020,Human_RBP_ID_23502774,Human_RBP_ID_24403149,Human_RBP_ID_27411154 Human_Splice_Rec_1226671,Human_Splice_Rec_1226677,Human_Splice_Rec_1226685,Human_Splice_Rec_1226694,Human_Splice_Rec_1226695,Human_Splice_Rec_1226704,Human_Splice_Rec_1226705,Human_Splice_Rec_1226710,Human_Splice_Rec_1226711,Human_Splice_Rec_1226718,Human_Splice_Rec_1226719,Human_Splice_Rec_1226730,Human_Splice_Rec_1226731,Human_Splice_Rec_1226740,Human_Splice_Rec_1226741,Human_Splice_Rec_1226748,Human_Splice_Rec_1226749,Human_Splice_Rec_1226755,Human_Splice_Rec_1226760,Human_Splice_Rec_1226761,Human_Splice_Rec_1226766,Human_Splice_Rec_1226767,Human_Splice_Rec_1226774,Human_Splice_Rec_1226775,Human_Splice_Rec_1226782,Human_Splice_Rec_1226783,Human_Splice_Rec_1226790,Human_Splice_Rec_1226791,Human_Splice_Rec_1226802,Human_Splice_Rec_1226803 Human_miRNA_ID_2239595,Human_miRNA_ID_2704613,Human_miRNA_ID_3016887 RMVar_hsa_circ_77179,RMVar_hsa_circ_148980,RMVar_hsa_circ_17880,RMVar_hsa_circ_377309,RMVar_hsa_circ_148982 104687 RMVar_ID_104687 Human_SNP_ID_461609192 m1A Human chr11 + 33722461 33722461 33722461 CCTCCTTGGATTCCCATTGTGATTGTCCACAGAACCTGGAAGGAAGGGACAGGAAGGAATGTCAG CCTCCTTGGATTCCCATTGTGATTGTCCACAGCACCTGGAAGGAAGGGACAGGAAGGAATGTCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:33722426..33722475 26863196 MeRIP-seq:(Medium) rs754137977 Functional Loss SNV dbSNP153 33..33 33 - - - 104688 RMVar_ID_104688 Human_SNP_ID_461609193 m1A Human chr11 + 33722461 33722461 33722461 CCTCCTTGGATTCCCATTGTGATTGTCCACAGAACCTGGAAGGAAGGGACAGGAAGGAATGTCAG CCTCCTTGGATTCCCATTGTGATTGTCCACAGGACCTGGAAGGAAGGGACAGGAAGGAATGTCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:33722426..33722475 26863196 MeRIP-seq:(Medium) rs754137977 Functional Loss SNV dbSNP153 33..33 33 - - - 104689 RMVar_ID_104689 Human_SNP_ID_461613767 m1A Human chr11 - 33742011 33742009 33742012 GGAGGAGGAAGAGGAGGAAGACGAGGATGATGATTCAGCAGATATGGATGAATCAGATGAAGATG GGAGGAGGAAGAGGAGGAAGACGAGGATGAT___TCAGCAGATATGGATGAATCAGATGAAGATG AATC A FBXO3 Ensembl:ENSG00000110429 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:33741960..33742032 26863196 MeRIP-seq:(Medium) rs754563184 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_6069818,Human_RBP_ID_26319688 Human_Splice_Rec_1226824,Human_Splice_Rec_1226844,Human_Splice_Rec_1226864,Human_Splice_Rec_1226892,Human_Splice_Rec_1226902 104690 RMVar_ID_104690 Human_SNP_ID_461613770 m1A Human chr11 + 33742016 33742016 33742016 TCATCTGATTCATCCATATCTGCTGAATCATCATCCTCGTCTTCCTCCTCTTCCTCCTCCTCCTC TCATCTGATTCATCCATATCTGCTGAATCATCCTCCTCGTCTTCCTCCTCTTCCTCCTCCTCCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:33741965..33742036 26863196 MeRIP-seq:(Medium) rs1564983959 Functional Loss SNV dbSNP153 33..33 33 - - - 104691 RMVar_ID_104691 Human_SNP_ID_461620719 m1A Human chr11 - 33774283 33774283 33774283 CGCTGACAGGACCCGAGCTTCCGCGACACCAGAAGGTGACGCCAGGGCCGCCCTCATCCTGCGGA CGCTGACAGGACCCGAGCTTCCGCGACACCAGGAGGTGACGCCAGGGCCGCCCTCATCCTGCGGA T C FBXO3 Ensembl:ENSG00000110429 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:33774263..33774356 26863196 MeRIP-seq:(Medium) rs1159595496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5313579,Human_RBP_ID_5342177,Human_RBP_ID_19049175,Human_RBP_ID_21965244 104692 RMVar_ID_104692 Human_SNP_ID_461620774 m1A Human chr11 - 33774464 33774464 33774464 TGGCGGCCATGGAGACCGAGACGGCGCCGCTGACCCTAGAGTCGCTGCCCACCGATCCCCTGCTC TGGCGGCCATGGAGACCGAGACGGCGCCGCTGGCCCTAGAGTCGCTGCCCACCGATCCCCTGCTC T C FBXO3 Ensembl:ENSG00000110429 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:33774228..33774465 26863196 MeRIP-seq:(Medium) rs1448273011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184746 Human_Splice_Rec_1226825,Human_Splice_Rec_1226845,Human_Splice_Rec_1226865,Human_Splice_Rec_1226903,Human_Splice_Rec_1226927,Human_Splice_Rec_1226945,Human_Splice_Rec_1226961 104693 RMVar_ID_104693 Human_SNP_ID_461687321 m1A Human chr11 + 34051768 34051768 34051768 GGAGCGGCTCTCGGTGCAGCGGGACAGGGCGAAGCGGCCTGCGCCCACGGAGCGCGCGACACTGC GGAGCGGCTCTCGGTGCAGCGGGACAGGGCGAGGCGGCCTGCGCCCACGGAGCGCGCGACACTGC A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr11:34051676..34052116;chr11:34051701..34051944;chr11:34051701..34051884 26863196 MeRIP-seq:(Medium) rs1416732924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226563,Human_RBP_ID_4158613,Human_RBP_ID_8773397,Human_RBP_ID_9275499,Human_RBP_ID_18416805 RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_148986,RMVar_hsa_circ_148987 104694 RMVar_ID_104694 Human_SNP_ID_461687363 m1A Human chr11 + 34051851 34051851 34051851 CTTGCCCCCTCAGCTGCCCACTCGTGATTTCCAGCGGCCTCCGCGCGCGCACGGTGAGCGCCACC CTTGCCCCCTCAGCTGCCCACTCGTGATTTCCTGCGGCCTCCGCGCGCGCACGGTGAGCGCCACC A T CAPRIN1 Ensembl:ENSG00000135387 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:34051701..34051899 26863196 MeRIP-seq:(Medium) rs552069117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184750,Human_RBP_ID_5461112,Human_RBP_ID_8774039,Human_RBP_ID_9275501,Human_RBP_ID_9362100,Human_RBP_ID_22034358 Human_Splice_Rec_1227037,Human_Splice_Rec_1227071,Human_Splice_Rec_1227073,Human_Splice_Rec_1227105,Human_Splice_Rec_1227115 RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_148986,RMVar_hsa_circ_148987 104695 RMVar_ID_104695 Human_SNP_ID_461687631 m1A Human chr11 + 34052317 34052317 34052317 CGCGCCCCCTCCCCCACCCGCTCGCGTAGGCTACCGCTCGCTGCGCGTTTTGTCCCGCGTCTCGC CGCGCCCCCTCCCCCACCCGCTCGCGTAGGCTGCCGCTCGCTGCGCGTTTTGTCCCGCGTCTCGC A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:34052316..34052635 26863196 MeRIP-seq:(Medium) rs1305901614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4158616 RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_148986,RMVar_hsa_circ_148987 104696 RMVar_ID_104696 Human_SNP_ID_461687726 m1A Human chr11 + 34052436 34052436 34052436 CTCCTTGCGGTCTGAAGATGCCCTCGGCCACCAGCCACAGCGGGAGCGGCAGCAAGTCGTCCGGA CTCCTTGCGGTCTGAAGATGCCCTCGGCCACCGGCCACAGCGGGAGCGGCAGCAAGTCGTCCGGA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:34052326..34052548 26863196 MeRIP-seq:(Medium) rs1217205735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226565,Human_RBP_ID_869688,Human_RBP_ID_986934,Human_RBP_ID_9321359,Human_RBP_ID_9362102,Human_RBP_ID_18432655,Human_RBP_ID_23503013 Human_Splice_Rec_1227038,Human_Splice_Rec_1227072,Human_Splice_Rec_1227074,Human_Splice_Rec_1227106,Human_Splice_Rec_1227124 Human_miRNA_ID_2051700,Human_miRNA_ID_2051701 RMVar_hsa_circ_88503,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_107391,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,RMVar_hsa_circ_148987,RMVar_hsa_circ_110279,RMVar_hsa_circ_95607,RMVar_hsa_circ_11121,RMVar_hsa_circ_148989,RMVar_hsa_circ_148991,RMVar_hsa_circ_148993,RMVar_hsa_circ_76656,RMVar_hsa_circ_148992,RMVar_hsa_circ_148990,RMVar_hsa_circ_148988 104697 RMVar_ID_104697 Human_SNP_ID_461687796 m1A Human chr11 - 34052534 34052534 34052534 ACAGCGCCGGTGCCGGTTGCGGGGTGCTGAGAAGCCGGCGCGGCGGCCCCGGCTCCCGCGGCCGC ACAGCGCCGGTGCCGGTTGCGGGGTGCTGAGAGGCCGGCGCGGCGGCCCCGGCTCCCGCGGCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr11:34052212..34052600;chr11:34052464..34052551 26863410 MeRIP-seq:(Medium) rs780159062 Functional Loss SNV dbSNP153 33..33 33 - - - 104698 RMVar_ID_104698 Human_SNP_ID_461687797 m1A Human chr11 - 34052534 34052534 34052534 ACAGCGCCGGTGCCGGTTGCGGGGTGCTGAGAAGCCGGCGCGGCGGCCCCGGCTCCCGCGGCCGC ACAGCGCCGGTGCCGGTTGCGGGGTGCTGAGACGCCGGCGCGGCGGCCCCGGCTCCCGCGGCCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr11:34052212..34052600;chr11:34052464..34052551 26863410 MeRIP-seq:(Medium) rs780159062 Functional Loss SNV dbSNP153 33..33 33 - - - 104699 RMVar_ID_104699 Human_SNP_ID_461688178 m1A Human chr11 + 34053423 34053423 34053423 GATTTAGATTCGTTGGGGGCTGGGTCCTGGGGAGACTGGAGAGGATGGCTGGGACTCGGGGCACA GATTTAGATTCGTTGGGGGCTGGGTCCTGGGGGGACTGGAGAGGATGGCTGGGACTCGGGGCACA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:34053419..34053566;chr11:34053420..34053533 26863196 MeRIP-seq:(Medium) rs1329852549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808501,Human_RBP_ID_6070198,Human_RBP_ID_8063373,Human_RBP_ID_9414856,Human_RBP_ID_11605020,Human_RBP_ID_18477649,Human_RBP_ID_23503015,Human_RBP_ID_26776229 Human_Splice_Rec_1227225 RMVar_hsa_circ_88503,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_107391,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,RMVar_hsa_circ_148987,RMVar_hsa_circ_110279,RMVar_hsa_circ_95607,RMVar_hsa_circ_11121,RMVar_hsa_circ_148989,RMVar_hsa_circ_148991,RMVar_hsa_circ_148993,RMVar_hsa_circ_76656,RMVar_hsa_circ_148992,RMVar_hsa_circ_148990,RMVar_hsa_circ_148988,RMVar_hsa_circ_148994,RMVar_hsa_circ_102755 104700 RMVar_ID_104700 Human_SNP_ID_461699479 m1A Human chr11 + 34092052 34092052 34092052 GAACAAACAGAGCTTCAGCAAGAACAGCTTCAAACAGGTACGAAATCCAGTGTCACCTCATTGGC GAACAAACAGAGCTTCAGCAAGAACAGCTTCACACAGGTACGAAATCCAGTGTCACCTCATTGGC A C CAPRIN1 Ensembl:ENSG00000135387 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:34091924..34095837 32194978 MeRIP-seq:(Medium) rs762432248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_871417,Human_RBP_ID_11606503,Human_RBP_ID_17233975 Human_Splice_Rec_1227063,Human_Splice_Rec_1227099,Human_Splice_Rec_1227155,Human_Splice_Rec_1227187,Human_Splice_Rec_1227217,Human_Splice_Rec_1227257,Human_Splice_Rec_1227265 RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_126497,RMVar_hsa_circ_148987,RMVar_hsa_circ_95607,RMVar_hsa_circ_6176,RMVar_hsa_circ_148991,RMVar_hsa_circ_148993,RMVar_hsa_circ_76656,RMVar_hsa_circ_148992,RMVar_hsa_circ_357235,RMVar_hsa_circ_343294,RMVar_hsa_circ_86955,RMVar_hsa_circ_149002,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_87599,RMVar_hsa_circ_84718,RMVar_hsa_circ_5766,RMVar_hsa_circ_33542,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_106228,RMVar_hsa_circ_295814,RMVar_hsa_circ_149020,RMVar_hsa_circ_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_335867,RMVar_hsa_circ_99463,RMVar_hsa_circ_272572,RMVar_hsa_circ_149027,RMVar_hsa_circ_149028,RMVar_hsa_circ_149030,RMVar_hsa_circ_115368,RMVar_hsa_circ_289121,RMVar_hsa_circ_149031,RMVar_hsa_circ_30298,RMVar_hsa_circ_149032,RMVar_hsa_circ_371871,RMVar_hsa_circ_84783,RMVar_hsa_circ_149034,RMVar_hsa_circ_149035 104701 RMVar_ID_104701 Human_SNP_ID_461703383 m1A Human chr11 + 34105689 34105664 34105689 GCCAGGCTTACTACGTGACCCGGACACCAGGCATACGCTAGGGGCAGTCAGCTGTGCCTTCTCTT GCCAGGCT_________________________TACGCTAGGGGCAGTCAGCTGTGCCTTCTCTT TTACTACGTGACCCGGACACCAGGCA T NAT10 Ensembl:ENSG00000135372 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:34105650..34105779 26863196 MeRIP-seq:(Medium) rs1191646940 Functional Loss DEL dbSNP153 9..33 33 - - - Human_RBP_ID_4184751,Human_RBP_ID_9275504,Human_RBP_ID_11607011,Human_RBP_ID_19632704,Human_RBP_ID_23117947 RMVar_hsa_circ_82096,RMVar_hsa_circ_149041 104702 RMVar_ID_104702 Human_SNP_ID_461703398 m1A Human chr11 + 34105689 34105689 34105689 GCCAGGCTTACTACGTGACCCGGACACCAGGCATACGCTAGGGGCAGTCAGCTGTGCCTTCTCTT GCCAGGCTTACTACGTGACCCGGACACCAGGCGTACGCTAGGGGCAGTCAGCTGTGCCTTCTCTT A G NAT10 Ensembl:ENSG00000135372 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:34105650..34105779 26863196 MeRIP-seq:(Medium) rs972942620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4184751,Human_RBP_ID_9275504,Human_RBP_ID_11607011,Human_RBP_ID_19632704,Human_RBP_ID_23117947 RMVar_hsa_circ_82096,RMVar_hsa_circ_149041 104703 RMVar_ID_104703 Human_SNP_ID_461703403 m1A Human chr11 - 34105695 34105695 34105695 CTCCGAAAGAGAAGGCACAGCTGACTGCCCCTAGCGTATGCCTGGTGTCCGGGTCACGTAGTAAG CTCCGAAAGAGAAGGCACAGCTGACTGCCCCTGGCGTATGCCTGGTGTCCGGGTCACGTAGTAAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:34105650..34105865 26863196 MeRIP-seq:(Medium) rs1410730557 Functional Loss SNV dbSNP153 33..33 33 - - - 104704 RMVar_ID_104704 Human_SNP_ID_461703432 m1A Human chr11 + 34105795 34105795 34105795 TGGCTGGGATCCCCCGGGCTCGGGGCGCAGGTACCCAACGCGGGAGGGCCGGGTATGGATGCCAA TGGCTGGGATCCCCCGGGCTCGGGGCGCAGGTGCCCAACGCGGGAGGGCCGGGTATGGATGCCAA A G NAT10 Ensembl:ENSG00000135372 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:34105790..34105918 32194978 MeRIP-seq:(Medium) rs1373181274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226556,Human_RBP_ID_867294,Human_RBP_ID_9321362,Human_RBP_ID_19049184 RMVar_hsa_circ_82096,RMVar_hsa_circ_149041 104705 RMVar_ID_104705 Human_SNP_ID_461711751 m1A Human chr11 + 34137323 34137323 34137323 ATTCTGGGAAAGGAGAGTGGACAGGAGGATCAAGGGTAATTCCTAGAGTTTTGGCTTGAGAAACT ATTCTGGGAAAGGAGAGTGGACAGGAGGATCAGGGGTAATTCCTAGAGTTTTGGCTTGAGAAACT A G NAT10 Ensembl:ENSG00000135372 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34137319..34137390 26863196 MeRIP-seq:(Medium) rs1403202741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31993,RMVar_hsa_circ_113445,RMVar_hsa_circ_149051,RMVar_hsa_circ_112036,RMVar_hsa_circ_114614,RMVar_hsa_circ_149058,RMVar_hsa_circ_149057,RMVar_hsa_circ_374627,RMVar_hsa_circ_90790,RMVar_hsa_circ_149059,RMVar_hsa_circ_149062,RMVar_hsa_circ_111709,RMVar_hsa_circ_96923,RMVar_hsa_circ_149064,RMVar_hsa_circ_149065,RMVar_hsa_circ_77613,RMVar_hsa_circ_149069 104706 RMVar_ID_104706 Human_SNP_ID_461711754 m1A Human chr11 - 34137346 34137346 34137346 CTCCGACAGCACCTCCAACACCCAGTTTCTCAAGCCAAAACTCTAGGAATTACCCTTGATCCTCC CTCCGACAGCACCTCCAACACCCAGTTTCTCACGCCAAAACTCTAGGAATTACCCTTGATCCTCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34137295..34137394 26863196 MeRIP-seq:(Medium) rs763256800 Functional Loss SNV dbSNP153 33..33 33 - - - 104707 RMVar_ID_104707 Human_SNP_ID_461713499 m1A Human chr11 - 34143509 34143509 34143509 CCTGGGCCCTCACCTTTTCAGGCTGATGATCGAGGCGTTCGGCCCAGCTTTGTTCAAAACTTCAT CCTGGGCCCTCACCTTTTCAGGCTGATGATCGTGGCGTTCGGCCCAGCTTTGTTCAAAACTTCAT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:34143426..34146217 26863196 MeRIP-seq:(Medium) rs1443716650 Functional Loss SNV dbSNP153 33..33 33 - - - 104708 RMVar_ID_104708 Human_SNP_ID_461713500 m1A Human chr11 - 34143509 34143509 34143509 CCTGGGCCCTCACCTTTTCAGGCTGATGATCGAGGCGTTCGGCCCAGCTTTGTTCAAAACTTCAT CCTGGGCCCTCACCTTTTCAGGCTGATGATCGGGGCGTTCGGCCCAGCTTTGTTCAAAACTTCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:34143426..34146217 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 104709 RMVar_ID_104709 Human_SNP_ID_461714150 m1A Human chr11 + 34146179 34146179 34146179 AGAGACAAAGAACAAAAAAGATATGAAACTGAAGCGGAAGAAATAGTGAAGAGAAACTCGGGCAT AGAGACAAAGAACAAAAAAGATATGAAACTGAGGCGGAAGAAATAGTGAAGAGAAACTCGGGCAT A G NAT10 Ensembl:ENSG00000135372 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:34146129..34146222 26863196 MeRIP-seq:(Medium) rs755007330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1778900,Human_RBP_ID_5549225,Human_RBP_ID_18607230,Human_RBP_ID_23503337,Human_RBP_ID_26319700,Human_RBP_ID_26890100,Human_RBP_ID_27803330 Human_Splice_Rec_1227332,Human_Splice_Rec_1227388,Human_Splice_Rec_1227416,Human_Splice_Rec_1227464,Human_Splice_Rec_1227470 RMVar_hsa_circ_77356,RMVar_hsa_circ_149072 104710 RMVar_ID_104710 Human_SNP_ID_461714338 m1A Human chr11 + 34146769 34146769 34146769 AGACCCACTGTCCCAGAAAAGCCTGATCCTGTAGTTTATGTAGAATGCCACATCTGCGTCCTCAA AGACCCACTGTCCCAGAAAAGCCTGATCCTGTGGTTTATGTAGAATGCCACATCTGCGTCCTCAA A G NAT10 Ensembl:ENSG00000135372 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:34146719..34146813 32194978 MeRIP-seq:(Medium) rs1379994061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108945,Human_RBP_ID_1161892,Human_RBP_ID_1778907,Human_RBP_ID_5110377,Human_RBP_ID_11607926,Human_RBP_ID_18607239,Human_RBP_ID_23206892,Human_RBP_ID_23503339,Human_RBP_ID_26408326,Human_RBP_ID_27411235 Human_miRNA_ID_275037 RMVar_hsa_circ_77356,RMVar_hsa_circ_149072 104711 RMVar_ID_104711 Human_SNP_ID_461716086 m1A Human chr11 + 34153117 34153117 34153117 GAGGTAAAGCCAACGTGACAGGATGGCTTGTGAGAGGCCAGGGGAGGCCTGGGGACACCAGTTGT GAGGTAAAGCCAACGTGACAGGATGGCTTGTGGGAGGCCAGGGGAGGCCTGGGGACACCAGTTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34153072..34153321 26863196 MeRIP-seq:(Medium) rs1389252297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6070739,Human_RBP_ID_11608127 104712 RMVar_ID_104712 Human_SNP_ID_461720732 m1A Human chr11 + 34169801 34169801 34169801 CACCCCACACTCCTTATGTCCCTTTCCCTGGAATCCCTTCCTGACTCCTCTCTGCTCCGTCCCCA CACCCCACACTCCTTATGTCCCTTTCCCTGGATTCCCTTCCTGACTCCTCTCTGCTCCGTCCCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34169793..34169919 26863196 MeRIP-seq:(Medium) rs1470519004 Functional Loss SNV dbSNP153 33..33 33 - - - 104713 RMVar_ID_104713 Human_SNP_ID_461727685 m1A Human chr11 + 34197418 34197418 34197418 GTGGACACCGCAGAAAGTAGTAGAGCGTGTGGAGGGCGTCGGGGGACCAAGTGATGGGCTGTGGC GTGGACACCGCAGAAAGTAGTAGAGCGTGTGGGGGGCGTCGGGGGACCAAGTGATGGGCTGTGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34197371..34197479 26863196 MeRIP-seq:(Medium) rs758727629 Functional Loss SNV dbSNP153 33..33 33 - - - 104714 RMVar_ID_104714 Human_SNP_ID_461727690 m1A Human chr11 - 34197424 34197424 34197424 CCAGCCGCCACAGCCCATCACTTGGTCCCCCGACGCCCTCCACACGCTCTACTACTTTCTGCGGT CCAGCCGCCACAGCCCATCACTTGGTCCCCCGGCGCCCTCCACACGCTCTACTACTTTCTGCGGT T C ABTB2 Ensembl:ENSG00000166016 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:34173256..34197523 26863196 MeRIP-seq:(Medium) rs780847451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1227477,Human_Splice_Rec_1227509 RMVar_hsa_circ_295052,RMVar_hsa_circ_149074 104715 RMVar_ID_104715 Human_SNP_ID_461729410 m1A Human chr11 - 34204626 34204626 34204626 TACAACGGCGGGTCCCTGGGCCATGACGAGCGAGCCGATGCCTATGCCCAGCTGGAGCTCCGAAC TACAACGGCGGGTCCCTGGGCCATGACGAGCGGGCCGATGCCTATGCCCAGCTGGAGCTCCGAAC T C ABTB2 Ensembl:ENSG00000166016 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34204511..34204629 26863196 MeRIP-seq:(Medium) rs758035917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1227474,Human_Splice_Rec_1227475,Human_Splice_Rec_1227506,Human_Splice_Rec_1227507 RMVar_hsa_circ_24796,RMVar_hsa_circ_295052,RMVar_hsa_circ_149074 104716 RMVar_ID_104716 Human_SNP_ID_461754410 m1A Human chr11 - 34310288 34310288 34310288 AGCTTTAATTGAGAGAGGGAGAGACACAGGACAGGGGCCAAGTTTAGGGTATCTGTGGAATAATA AGCTTTAATTGAGAGAGGGAGAGACACAGGACGGGGGCCAAGTTTAGGGTATCTGTGGAATAATA T C ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34310285..34310654 26863196 MeRIP-seq:(Medium) rs115426848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9638780 104717 RMVar_ID_104717 Human_SNP_ID_461754447 m1A Human chr11 - 34310476 34310476 34310476 AGGAAACCCACAAGGGCACCATGGAGTACTTCAGGGGAGAGGCAAGGCAAGCTTGGGGACGTGAG AGGAAACCCACAAGGGCACCATGGAGTACTTCGGGGGAGAGGCAAGGCAAGCTTGGGGACGTGAG T C ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:34310457..34310586 26863196 MeRIP-seq:(Medium) rs919667075 Functional Loss SNV dbSNP153 33..33 33 - - - 104718 RMVar_ID_104718 Human_SNP_ID_461763183 m1A Human chr11 - 34348495 34348495 34348495 AGAGCCCCCAGAGGCTTCCAGGCAGAGGGAACAGTGTGAGCAAAGACCTGGAAGCCAACGCATAT AGAGCCCCCAGAGGCTTCCAGGCAGAGGGAACGGTGTGAGCAAAGACCTGGAAGCCAACGCATAT T C ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34348493..34348620 26863196 MeRIP-seq:(Medium) rs926086308 Functional Loss SNV dbSNP153 33..33 33 - - - 104719 RMVar_ID_104719 Human_SNP_ID_461763771 m1A Human chr11 + 34351042 34351042 34351042 CTATTACTACAGCTGCATAAGAGTAGAAATAGAGGCGAAGCATCTACCCACTGACCTGTCGGACA CTATTACTACAGCTGCATAAGAGTAGAAATAGGGGCGAAGCATCTACCCACTGACCTGTCGGACA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:34350998..34351124 26863196 MeRIP-seq:(Medium) rs1313929212 Functional Loss SNV dbSNP153 33..33 33 - - - 104720 RMVar_ID_104720 Human_SNP_ID_461765072 m1A Human chr11 + 34356795 34356795 34356795 TCGTTGTTGATGACCATCTCCAGGGCCTCAGCAGACACCTCCCCGCCTCCGGCCCCTCCGCCATC TCGTTGTTGATGACCATCTCCAGGGCCTCAGCCGACACCTCCCCGCCTCCGGCCCCTCCGCCATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34356706..34356832 26863196 MeRIP-seq:(Medium) rs147157814 Functional Loss SNV dbSNP153 33..33 33 - - - 104721 RMVar_ID_104721 Human_SNP_ID_461765073 m1A Human chr11 + 34356795 34356795 34356795 TCGTTGTTGATGACCATCTCCAGGGCCTCAGCAGACACCTCCCCGCCTCCGGCCCCTCCGCCATC TCGTTGTTGATGACCATCTCCAGGGCCTCAGCGGACACCTCCCCGCCTCCGGCCCCTCCGCCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:34356706..34356832 26863196 MeRIP-seq:(Medium) rs147157814 Functional Loss SNV dbSNP153 33..33 33 - - - 104722 RMVar_ID_104722 Human_SNP_ID_461765442 m1A Human chr11 - 34357728 34357728 34357728 GGATCTCGGCCACCTTCCCGCGGCCTCCGGGCAGGCAATGCGGCCGCCGAGCCCCGCGACGCAGA GGATCTCGGCCACCTTCCCGCGGCCTCCGGGCGGGCAATGCGGCCGCCGAGCCCCGCGACGCAGA T C ABTB2 Ensembl:ENSG00000166016 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:34357701..34358000 26863196 MeRIP-seq:(Medium) rs3740796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5520658 104723 RMVar_ID_104723 Human_SNP_ID_461789588 m1A Human chr11 + 34456809 34456809 34456809 TGCCACCTGGCATTGAGGCCAGTCCTGACAAAATGCTTCAGGTGAGCCTGGTGGATTGAGATGTT TGCCACCTGGCATTGAGGCCAGTCCTGACAAACTGCTTCAGGTGAGCCTGGTGGATTGAGATGTT A C CAT Ensembl:ENSG00000121691 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:34456721..34456822 32194978 MeRIP-seq:(Medium) rs1186832232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867308,Human_RBP_ID_19049206 Human_Splice_Rec_1227525,Human_Splice_Rec_1227547 RMVar_hsa_circ_341712,RMVar_hsa_circ_355367,RMVar_hsa_circ_364865,RMVar_hsa_circ_123065,RMVar_hsa_circ_118687,RMVar_hsa_circ_128068,RMVar_hsa_circ_149075,RMVar_hsa_circ_149076,RMVar_hsa_circ_314621,RMVar_hsa_circ_111129,RMVar_hsa_circ_149077,RMVar_hsa_circ_149078,RMVar_hsa_circ_292742,RMVar_hsa_circ_62794,RMVar_hsa_circ_109472,RMVar_hsa_circ_149079,RMVar_hsa_circ_149080,RMVar_hsa_circ_149081 104724 RMVar_ID_104724 Human_SNP_ID_461793213 m1A Human chr11 + 34471662 34471662 34471662 CAGTCATTTAAAAAAAAAATTTGTTTTGACGGATGATTGGATTATTCATTTAAAATGATTAGAAG CAGTCATTTAAAAAAAAAATTTGTTTTGACGGCTGATTGGATTATTCATTTAAAATGATTAGAAG A C CAT Ensembl:ENSG00000121691 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:34471612..34471712 32194978 MeRIP-seq:(Medium) rs1049324469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23206896,Human_RBP_ID_23503454 RMVar_hsa_circ_123065,RMVar_hsa_circ_118687,RMVar_hsa_circ_149075,RMVar_hsa_circ_111129,RMVar_hsa_circ_149078,RMVar_hsa_circ_102151,RMVar_hsa_circ_109472,RMVar_hsa_circ_149079,RMVar_hsa_circ_149081,RMVar_hsa_circ_149083,RMVar_hsa_circ_149085,RMVar_hsa_circ_123859,RMVar_hsa_circ_116136,RMVar_hsa_circ_149087 104725 RMVar_ID_104725 Human_SNP_ID_461793214 m1A Human chr11 + 34471662 34471662 34471662 CAGTCATTTAAAAAAAAAATTTGTTTTGACGGATGATTGGATTATTCATTTAAAATGATTAGAAG CAGTCATTTAAAAAAAAAATTTGTTTTGACGGGTGATTGGATTATTCATTTAAAATGATTAGAAG A G CAT Ensembl:ENSG00000121691 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:34471612..34471712 32194978 MeRIP-seq:(Medium) rs1049324469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23206896,Human_RBP_ID_23503454 RMVar_hsa_circ_123065,RMVar_hsa_circ_118687,RMVar_hsa_circ_149075,RMVar_hsa_circ_111129,RMVar_hsa_circ_149078,RMVar_hsa_circ_102151,RMVar_hsa_circ_109472,RMVar_hsa_circ_149079,RMVar_hsa_circ_149081,RMVar_hsa_circ_149083,RMVar_hsa_circ_149085,RMVar_hsa_circ_123859,RMVar_hsa_circ_116136,RMVar_hsa_circ_149087 104726 RMVar_ID_104726 Human_SNP_ID_461793215 m1A Human chr11 + 34471662 34471662 34471662 CAGTCATTTAAAAAAAAAATTTGTTTTGACGGATGATTGGATTATTCATTTAAAATGATTAGAAG CAGTCATTTAAAAAAAAAATTTGTTTTGACGGTTGATTGGATTATTCATTTAAAATGATTAGAAG A T CAT Ensembl:ENSG00000121691 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:34471612..34471712 32194978 MeRIP-seq:(Medium) rs1049324469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23206896,Human_RBP_ID_23503454 RMVar_hsa_circ_123065,RMVar_hsa_circ_118687,RMVar_hsa_circ_149075,RMVar_hsa_circ_111129,RMVar_hsa_circ_149078,RMVar_hsa_circ_102151,RMVar_hsa_circ_109472,RMVar_hsa_circ_149079,RMVar_hsa_circ_149081,RMVar_hsa_circ_149083,RMVar_hsa_circ_149085,RMVar_hsa_circ_123859,RMVar_hsa_circ_116136,RMVar_hsa_circ_149087 104727 RMVar_ID_104727 Human_SNP_ID_461902232 m1A Human chr11 + 34916239 34916239 34916239 CACCGGTGGCCCCGCCCCTACCTGCGCGCCGCATCTCCGGGAACAACAGTCTCCCTCCCGAGCAT CACCGGTGGCCCCGCCCCTACCTGCGCGCCGCTTCTCCGGGAACAACAGTCTCCCTCCCGAGCAT A T PDHX Ensembl:ENSG00000110435 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:34916234..34916338 26863196 MeRIP-seq:(Medium) rs1470302738 Functional Loss SNV dbSNP153 33..33 33 - - - 104728 RMVar_ID_104728 Human_SNP_ID_461902268 m1A Human chr11 + 34916314 34916314 34916314 CATGGCCCAGACCAGGGACCCGCGCGGCCTCCAATCTCCGCACGGCTTTGCGCGCGGCGCTTAGC CATGGCCCAGACCAGGGACCCGCGCGGCCTCCGATCTCCGCACGGCTTTGCGCGCGGCGCTTAGC A G PDHX Ensembl:ENSG00000110435 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34916207..34916342 26863196 MeRIP-seq:(Medium) rs567329509 Functional Loss SNV dbSNP153 33..33 33 - - - 104729 RMVar_ID_104729 Human_SNP_ID_461917904 m1A Human chr11 + 34978934 34978934 34978934 GTGATCTGACTTATACTTCAGAAACGAAAAGGAGAGGCTGCCCTGGGTGCTGTGTAGAATGTAGC GTGATCTGACTTATACTTCAGAAACGAAAAGGGGAGGCTGCCCTGGGTGCTGTGTAGAATGTAGC A G PDHX Ensembl:ENSG00000110435 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34978922..34979029 26863196 MeRIP-seq:(Medium) rs1229387268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46641,RMVar_hsa_circ_293194,RMVar_hsa_circ_368092,RMVar_hsa_circ_149099,RMVar_hsa_circ_306454,RMVar_hsa_circ_149102,RMVar_hsa_circ_149103,RMVar_hsa_circ_303558,RMVar_hsa_circ_272750,RMVar_hsa_circ_149104,RMVar_hsa_circ_149105,RMVar_hsa_circ_363424,RMVar_hsa_circ_308560,RMVar_hsa_circ_149110,RMVar_hsa_circ_271717,RMVar_hsa_circ_39252,RMVar_hsa_circ_149112,RMVar_hsa_circ_32966 104730 RMVar_ID_104730 Human_SNP_ID_461957111 m1A Human chr11 - 35139230 35139230 35139230 AGGATCCCTGGGCGCGGGGCAGGGGCCGGCGGAGGACGGGACGAGGATGGCGGACCGAACCTGGC AGGATCCCTGGGCGCGGGGCAGGGGCCGGCGGTGGACGGGACGAGGATGGCGGACCGAACCTGGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:35139118..35139402;chr11:35139126..35139432;chr11:35139084..35139406;chr11:35139023..35139421;chr11:35139151..35139410 26863196 MeRIP-seq:(Medium) rs781691339 Functional Loss SNV dbSNP153 33..33 33 - - - 104731 RMVar_ID_104731 Human_SNP_ID_461966420 m1A Human chr11 - 35176518 35176518 35176518 GATTCTTTTGCATAAATAATTTGGAGACAGTAATAAGTTCAGTTTAGGACAGACTCCTTAAAAAG GATTCTTTTGCATAAATAATTTGGAGACAGTAGTAAGTTCAGTTTAGGACAGACTCCTTAAAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:35176516..35176681 26863196 MeRIP-seq:(Medium) rs1306559228 Functional Loss SNV dbSNP153 33..33 33 - - - 104732 RMVar_ID_104732 Human_SNP_ID_461966423 m1A Human chr11 - 35176524 35176524 35176524 ATGTTAGATTCTTTTGCATAAATAATTTGGAGACAGTAATAAGTTCAGTTTAGGACAGACTCCTT ATGTTAGATTCTTTTGCATAAATAATTTGGAGGCAGTAATAAGTTCAGTTTAGGACAGACTCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:35176522..35176611 26863196 MeRIP-seq:(Medium) rs765612909 Functional Loss SNV dbSNP153 33..33 33 - - - 104733 RMVar_ID_104733 Human_SNP_ID_461966453 m1A Human chr11 - 35176624 35176624 35176624 GCGGCCTCCGTCCGAGAGATGCTGTAGCGACCATTTTTCTCCACGTGGAATACACCTGCAAAGCG GCGGCCTCCGTCCGAGAGATGCTGTAGCGACCGTTTTTCTCCACGTGGAATACACCTGCAAAGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:35176533..35176681 26863196 MeRIP-seq:(Medium) rs1292289106 Functional Loss SNV dbSNP153 33..33 33 - - - 104734 RMVar_ID_104734 Human_SNP_ID_461979709 m1A Human chr11 + 35229280 35229280 35229280 AGGAGTCGTCAGAAACTCCAGACCAGTTTATGACAGCTGATGAGACAAGGAACCTGCAGAATGTG AGGAGTCGTCAGAAACTCCAGACCAGTTTATGGCAGCTGATGAGACAAGGAACCTGCAGAATGTG A G CD44 Ensembl:ENSG00000026508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:35229131..35229279 26863196 MeRIP-seq:(Medium) rs775588163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29302,Human_RBP_ID_2267769,Human_RBP_ID_5549233,Human_RBP_ID_8350790,Human_RBP_ID_22380601,Human_RBP_ID_22754121 RMVar_hsa_circ_86428,RMVar_hsa_circ_149117 104735 RMVar_ID_104735 Human_SNP_ID_462071750 m1A Human chr11 - 35618692 35618692 35618692 GGAGCCCTCCCCACAGCGCCAGCAGCGAGCCCAGCGCCAGCAGCCAGAGCCCCGCGGTGGCGGCG GGAGCCCTCCCCACAGCGCCAGCAGCGAGCCCGGCGCCAGCAGCCAGAGCCCCGCGGTGGCGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:35618641..35619188 26863196 MeRIP-seq:(Medium) rs1347735978 Functional Loss SNV dbSNP153 33..33 33 - - - 104736 RMVar_ID_104736 Human_SNP_ID_462072067 m1A Human chr11 + 35619339 35619339 35619339 AGGTGCAGGAGGAGCTGCGCGCTGCGCACTGGACCGAGGGCAGCGTGGTGAGCCTGACACGCTGG AGGTGCAGGAGGAGCTGCGCGCTGCGCACTGGCCCGAGGGCAGCGTGGTGAGCCTGACACGCTGG A C FJX1 Ensembl:ENSG00000179431 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:35619291..35619365 26863196 MeRIP-seq:(Medium) rs1444545444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4159118,Human_RBP_ID_27201132,Human_RBP_ID_27411291 104737 RMVar_ID_104737 Human_SNP_ID_462072279 m1A Human chr11 + 35619747 35619747 35619747 TGTTGCAGTCAGTGTGCGTGTTCCGCGAGCGGACCGCGCGGCGCGTCCTGGAGCTGCACCGCGGA TGTTGCAGTCAGTGTGCGTGTTCCGCGAGCGGGCCGCGCGGCGCGTCCTGGAGCTGCACCGCGGA A G FJX1 Ensembl:ENSG00000179431 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:35619702..35619900 26863196 MeRIP-seq:(Medium) rs202089278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395740 104738 RMVar_ID_104738 Human_SNP_ID_462072288 m1A Human chr11 + 35619766 35619766 35619766 GTTCCGCGAGCGGACCGCGCGGCGCGTCCTGGAGCTGCACCGCGGACAGGACGCCGCGGCCCGGC GTTCCGCGAGCGGACCGCGCGGCGCGTCCTGGTGCTGCACCGCGGACAGGACGCCGCGGCCCGGC A T FJX1 Ensembl:ENSG00000179431 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:35619717..35619868 32194978 MeRIP-seq:(Medium) rs1452300687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395740 104739 RMVar_ID_104739 Human_SNP_ID_462083017 m1A Human chr11 + 35663448 35663430 35663448 AGGAAGAGAGCGAGTCAGAGGAAGAGAGCGAGACAGAGGAAGAGAGTGAGGATGAGAGCGATGAG AGGAAGAGAGCGAGT__________________CAGAGGAAGAGAGTGAGGATGAGAGCGATGAG TCAGAGGAAGAGAGCGAGA T TRIM44 Ensembl:ENSG00000166326 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:35662726..35663775;chr11:35662701..35685350 26863196 MeRIP-seq:(Medium) rs1407966062 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_193330,Human_RBP_ID_750077,Human_RBP_ID_808940,Human_RBP_ID_4190166,Human_RBP_ID_6071367,Human_RBP_ID_9343944,Human_RBP_ID_22034362,Human_RBP_ID_22895013,Human_RBP_ID_23113065,Human_RBP_ID_23117862,Human_RBP_ID_23503782,Human_RBP_ID_24542316,Human_RBP_ID_24557179,Human_RBP_ID_24883825,Human_RBP_ID_26318206,Human_RBP_ID_27804357 RMVar_hsa_circ_127668,RMVar_hsa_circ_268949,RMVar_hsa_circ_149164 104740 RMVar_ID_104740 Human_SNP_ID_462083026 m1A Human chr11 + 35663448 35663448 35663448 AGGAAGAGAGCGAGTCAGAGGAAGAGAGCGAGACAGAGGAAGAGAGTGAGGATGAGAGCGATGAG AGGAAGAGAGCGAGTCAGAGGAAGAGAGCGAGTCAGAGGAAGAGAGTGAGGATGAGAGCGATGAG A T TRIM44 Ensembl:ENSG00000166326 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:35662726..35663775;chr11:35662701..35685350 26863196 MeRIP-seq:(Medium) rs1196630044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193330,Human_RBP_ID_750077,Human_RBP_ID_808940,Human_RBP_ID_4190166,Human_RBP_ID_6071367,Human_RBP_ID_9343944,Human_RBP_ID_22034362,Human_RBP_ID_22895013,Human_RBP_ID_23113065,Human_RBP_ID_23117862,Human_RBP_ID_23503782,Human_RBP_ID_24542316,Human_RBP_ID_24557179,Human_RBP_ID_24883825,Human_RBP_ID_26318206,Human_RBP_ID_27804357 RMVar_hsa_circ_127668,RMVar_hsa_circ_268949,RMVar_hsa_circ_149164 104741 RMVar_ID_104741 Human_SNP_ID_462083107 m1A Human chr11 + 35663653 35663653 35663653 AGCAGAGAGAGTGGCCAAGAGGAAGTGTCCGGACCATGGGCTTGATTTGAGTACCTATTGCCAGG AGCAGAGAGAGTGGCCAAGAGGAAGTGTCCGGGCCATGGGCTTGATTTGAGTACCTATTGCCAGG A G TRIM44 Ensembl:ENSG00000166326 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:35663603..35685331 32194978 MeRIP-seq:(Medium) rs202091709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_192952,Human_RBP_ID_867316,Human_RBP_ID_1462027,Human_RBP_ID_3938987,Human_RBP_ID_6071371,Human_RBP_ID_8350815,Human_RBP_ID_8769259,Human_RBP_ID_9362133,Human_RBP_ID_11610156,Human_RBP_ID_18188461,Human_RBP_ID_18607365,Human_RBP_ID_19028248,Human_RBP_ID_22034363,Human_RBP_ID_22895014,Human_RBP_ID_23503786,Human_RBP_ID_24542318,Human_RBP_ID_26318207,Human_RBP_ID_27201157,Human_RBP_ID_27803340 Human_miRNA_ID_3097778 RMVar_hsa_circ_127668,RMVar_hsa_circ_268949,RMVar_hsa_circ_149164 104742 RMVar_ID_104742 Human_SNP_ID_462098457 m1A Human chr11 - 35725903 35725903 35725903 GTCCCGAGTTACCTTTAGAACAGAGACAAATAAGAAGAATAAGTTGAACATACAAAGAAACAAAA GTCCCGAGTTACCTTTAGAACAGAGACAAATAGGAAGAATAAGTTGAACATACAAAGAAACAAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:35725901..35725975 26863196 MeRIP-seq:(Medium) rs779677289 Functional Loss SNV dbSNP153 33..33 33 - - - 104743 RMVar_ID_104743 Human_SNP_ID_462118748 m1A Human chr11 - 35810056 35810056 35810056 CCTTCAGGGCTGTCACTTTGACTCAGTGCCTTAGGAGCTAATGACCTTTGCTAGGGAATTGCTCT CCTTCAGGGCTGTCACTTTGACTCAGTGCCTTGGGAGCTAATGACCTTTGCTAGGGAATTGCTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:35810021..35810171 32194978 MeRIP-seq:(Medium) rs1319360691 Functional Loss SNV dbSNP153 33..33 33 - - - 104744 RMVar_ID_104744 Human_SNP_ID_462118749 m1A Human chr11 - 35810056 35810056 35810056 CCTTCAGGGCTGTCACTTTGACTCAGTGCCTTAGGAGCTAATGACCTTTGCTAGGGAATTGCTCT CCTTCAGGGCTGTCACTTTGACTCAGTGCCTTCGGAGCTAATGACCTTTGCTAGGGAATTGCTCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:35810021..35810171 32194978 MeRIP-seq:(Medium) rs1319360691 Functional Loss SNV dbSNP153 33..33 33 - - - 104745 RMVar_ID_104745 Human_SNP_ID_462157294 m1A Human chr11 - 35971703 35971703 35971703 CGCCCTGAGGCTCAATTCATCTTTTTGGTTCTATATTCGTACCCTGGGACTGCCATCACAAAATG CGCCCTGAGGCTCAATTCATCTTTTTGGTTCTGTATTCGTACCCTGGGACTGCCATCACAAAATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:35971696..35971954 26863196 MeRIP-seq:(Medium) rs756263085 Functional Loss SNV dbSNP153 33..33 33 - - - 104746 RMVar_ID_104746 Human_SNP_ID_462163959 m1A Human chr11 - 36000715 36000715 36000715 CCCCAGCTTGAAGACTCATGGCCTGCATGACCAAGGTTCCACCTGCCTTCCTACTTTCATCATCC CCCCAGCTTGAAGACTCATGGCCTGCATGACCGAGGTTCCACCTGCCTTCCTACTTTCATCATCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:36000712..36000930 26863196 MeRIP-seq:(Medium) rs571264283 Functional Loss SNV dbSNP153 33..33 33 - - - 104747 RMVar_ID_104747 Human_SNP_ID_462189774 m1A Human chr11 + 36108976 36108976 36108976 GAAACATCAGGGTAAGGGGGGATTCTGACTCAATGGACCTAACAGGATTCTCACTGAAGGCAGGC GAAACATCAGGGTAAGGGGGGATTCTGACTCAGTGGACCTAACAGGATTCTCACTGAAGGCAGGC A G LDLRAD3 Ensembl:ENSG00000179241 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:36108942..36109062 26863196 MeRIP-seq:(Medium) rs1048510993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259700,Human_RBP_ID_22521627 RMVar_hsa_circ_111093,RMVar_hsa_circ_149169,RMVar_hsa_circ_149172,RMVar_hsa_circ_94278,RMVar_hsa_circ_149173 104748 RMVar_ID_104748 Human_SNP_ID_462220474 m1A Human chr11 - 36236713 36236713 36236713 ATCTTTCTCCGCAGTGAGTTGACAATTATTCAAAGAATCTGAGAATAGGCTGTGAGCGGTGGTGT ATCTTTCTCCGCAGTGAGTTGACAATTATTCAGAGAATCTGAGAATAGGCTGTGAGCGGTGGTGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:36236606..36236750 26863196 MeRIP-seq:(Medium) rs1565325760 Functional Loss SNV dbSNP153 33..33 33 - - - 104749 RMVar_ID_104749 Human_SNP_ID_462254651 m1A Human chr11 + 36376427 36376427 36376427 GGAGGGAAACGTGTCACCAGCCCGGCTGTGGGAGCTCCGCGGCCGAAGCGTTTGTTGACTCGCGC GGAGGGAAACGTGTCACCAGCCCGGCTGTGGGGGCTCCGCGGCCGAAGCGTTTGTTGACTCGCGC A G PRR5L Ensembl:ENSG00000135362 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:36376381..36376700 26863196 MeRIP-seq:(Medium) rs997804415 Functional Loss SNV dbSNP153 33..33 33 - - - 104750 RMVar_ID_104750 Human_SNP_ID_462272368 m1A Human chr11 - 36453774 36453774 36453774 CCTCCAGGTAGTCTTCCCTGATTCCCTAGTCAAGATGAAATCCCTGTGCCCTGGGACCCGTGGCC CCTCCAGGTAGTCTTCCCTGATTCCCTAGTCAGGATGAAATCCCTGTGCCCTGGGACCCGTGGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:36453771..36454035 26863196 MeRIP-seq:(Medium) rs1179645529 Functional Loss SNV dbSNP153 33..33 33 - - - 104751 RMVar_ID_104751 Human_SNP_ID_462924015 m1A Human chr11 - 39024476 39024474 39024476 GAAAGAGAAAGAAAGAAAGAAAGAAAAAAAGAAAGAAAGAGCAGGCAAGCAGGGAGGGAGGAAGG GAAAGAGAAAGAAAGAAAGAAAGAAAAAAAGA__GAAAGAGCAGGCAAGCAGGGAGGGAGGAAGG CTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:39024354..39024655 26863196 MeRIP-seq:(Medium) rs1379752855 Functional Loss DEL dbSNP153 33..34 33 - - - 104752 RMVar_ID_104752 Human_SNP_ID_462958977 m1A Human chr11 - 39161694 39161694 39161694 CCCGCACATCATCCCTTATAGTCCCCACAACCACGGCGGTTTTGTTTTCCCGGCCAGGAAGCTTC CCCGCACATCATCCCTTATAGTCCCCACAACCGCGGCGGTTTTGTTTTCCCGGCCAGGAAGCTTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:39161674..39161822 26863196 MeRIP-seq:(Medium) rs1207820353 Functional Loss SNV dbSNP153 33..33 33 - - - 104753 RMVar_ID_104753 Human_SNP_ID_462959036 m1A Human chr11 - 39161821 39161821 39161821 ACACCTCTCGGCCTTTGAGAGGACCAGAGAGCAGGACGGTGCCACAGCCCTTGGGGGACTCTAGG ACACCTCTCGGCCTTTGAGAGGACCAGAGAGCGGGACGGTGCCACAGCCCTTGGGGGACTCTAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:39161712..39161821 26863196 MeRIP-seq:(Medium) rs12360759 Functional Loss SNV dbSNP153 33..33 33 - - - 104754 RMVar_ID_104754 Human_SNP_ID_463145319 m1A Human chr11 + 39868961 39868961 39868961 ACACACACACACAAACACACACACACACACACACGATGGCAGCTTTTCAGGAATTTGTGATCTCA ACACACACACACAAACACACACACACACACACTCGATGGCAGCTTTTCAGGAATTTGTGATCTCA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:39868947..39869074 26863196 MeRIP-seq:(Medium) rs1053202061 Functional Loss SNV dbSNP153 33..33 33 - - - 104755 RMVar_ID_104755 Human_SNP_ID_368923244 m1A Human chr8 - 75105291 75105285 75105292 TCTCAAAAAAAAAAAAAGAAGAAAAAGAAAGAAAGAAAGAAGAAAGAGAAAGAAAGGAAAGGAAA TCTCAAAAAAAAAAAAAGAAGAAAAAGAAAG_______GAAGAAAGAGAAAGAAAGGAAAGGAAA CTTTCTTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:75105243..75105326 26863196 MeRIP-seq:(Medium) rs1402998519 Functional Loss DEL dbSNP153 32..38 33 - - - 104756 RMVar_ID_104756 Human_SNP_ID_369063908 m1A Human chr8 + 75662895 75662893 75662896 AGGAGAAAGAAAGAGGAAAGAGAAAGAAAGAAAGAGAGAGAGAGAAAGAAAAAGAAAGAAAGAAA AGGAGAAAGAAAGAGGAAAGAGAAAGAAAGA___AGAGAGAGAGAAAGAAAAAGAAAGAAAGAAA AAAG A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:75662883..75662965 26863410 MeRIP-seq:(Medium) rs1190935216 Functional Loss DEL dbSNP153 32..34 33 - - - 104757 RMVar_ID_104757 Human_SNP_ID_369397330 m1A Human chr8 - 77000053 77000053 77000053 CCTTGGTAATCCAGATTCGGCTAGGAAAAGACAAGCTTTCCAGAGAATGTTTCAGAGAAAGTTAC CCTTGGTAATCCAGATTCGGCTAGGAAAAGACGAGCTTTCCAGAGAATGTTTCAGAGAAAGTTAC T C PEX2 Ensembl:ENSG00000164751 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:76999964..77000058 26863196 MeRIP-seq:(Medium) rs1201607799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4991537 Human_Splice_Rec_987339,Human_Splice_Rec_987346,Human_Splice_Rec_987347,Human_Splice_Rec_987349,Human_Splice_Rec_987358,Human_Splice_Rec_987359,Human_Splice_Rec_987365 104758 RMVar_ID_104758 Human_SNP_ID_369397524 m1A Human chr8 - 77000424 77000424 77000424 CCTGCCAGAGGCCCTTCGCGATGTCCGCAAGCAGAGAAAGCCCTGCCCTCCCAAGCCCCGGCTTC CCTGCCAGAGGCCCTTCGCGATGTCCGCAAGCGGAGAAAGCCCTGCCCTCCCAAGCCCCGGCTTC T C PEX2 Ensembl:ENSG00000164751 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:77000374..77000445 26863196 MeRIP-seq:(Medium) rs1268401409 Functional Loss SNV dbSNP153 33..33 33 - - - 104759 RMVar_ID_104759 Human_SNP_ID_369397536 m1A Human chr8 + 77000441 77000441 77000441 GGGCAGGGCTTTCTCTGCTTGCGGACATCGCGAAGGGCCTCTGGCAGGCGCCGCCGGGTGGCGGC GGGCAGGGCTTTCTCTGCTTGCGGACATCGCGGAGGGCCTCTGGCAGGCGCCGCCGGGTGGCGGC A G lnc-ZFHX4-6,lnc-ZFHX4-6:2,lnc-ZFHX4-6:3,lnc-ZFHX4-6:4,lnc-ZFHX4-6:5,lnc-ZFHX4-6:6,lnc-ZFHX4-6:7,lnc-ZFHX4-6:8,lnc-ZFHX4-6:9,lnc-ZFHX4-6:10,lnc-ZFHX4-6:11,lnc-ZFHX4-6:12,lnc-ZFHX4-6:13 RNACentral:URS0000D58F69,RNACentral:URS00008B5D59,RNACentral:URS00009AE468,RNACentral:URS0000D5A4A6,RNACentral:URS0000D5AC39,RNACentral:URS00008BBC5B,RNACentral:URS0000D58428,RNACentral:URS0000D5DECF,RNACentral:URS0000D5E2CC,RNACentral:URS0000D5DB04,RNACentral:URS0000D5AAAC,RNACentral:URS0000D5BFB9,RNACentral:URS0000D5A989 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron,exon,exon,intron,intron,exon,intron,intron,exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:77000391..77000613 26863196 MeRIP-seq:(Medium) rs1301598586 Functional Loss SNV dbSNP153 33..33 33 - - - 104760 RMVar_ID_104760 Human_SNP_ID_369823916 m1A Human chr8 + 78666153 78666153 78666153 GTCTCGCTGAGCTCGAGGAGGTGGCGCGATGGAGGGACTGGAAGGTGAGGCGATGAAGGGATGAG GTCTCGCTGAGCTCGAGGAGGTGGCGCGATGGCGGGACTGGAAGGTGAGGCGATGAAGGGATGAG A C ZC2HC1A Ensembl:ENSG00000104427 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:78666103..78666252 26863196 MeRIP-seq:(Medium) rs898680595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_987439,Human_Splice_Rec_987443,Human_Splice_Rec_987459 RMVar_hsa_circ_77072,RMVar_hsa_circ_252786,RMVar_hsa_circ_252788 104761 RMVar_ID_104761 Human_SNP_ID_370081124 m1A Human chr8 + 79767711 79767711 79767711 GTTCCTGGGGAGGGTCGGCGCGGCGGGCAGGGAGGAGTTAACTACAGCGGCGCCTCTCCGCTCTC GTTCCTGGGGAGGGTCGGCGCGGCGGGCAGGGGGGAGTTAACTACAGCGGCGCCTCTCCGCTCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:79767663..79767775 26863196 MeRIP-seq:(Medium) rs906626594 Functional Loss SNV dbSNP153 33..33 33 - - - 104762 RMVar_ID_104762 Human_SNP_ID_370081125 m1A Human chr8 + 79767711 79767711 79767711 GTTCCTGGGGAGGGTCGGCGCGGCGGGCAGGGAGGAGTTAACTACAGCGGCGCCTCTCCGCTCTC GTTCCTGGGGAGGGTCGGCGCGGCGGGCAGGGTGGAGTTAACTACAGCGGCGCCTCTCCGCTCTC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:79767663..79767775 26863196 MeRIP-seq:(Medium) rs906626594 Functional Loss SNV dbSNP153 33..33 33 - - - 104763 RMVar_ID_104763 Human_SNP_ID_370141749 m1A Human chr8 + 80030216 80030216 80030216 AAGAGAAACACTCGCAGAAAATGGCTCTCGGCAGCCACAGCACGGGTCCGACACAGCGCCGCCAT AAGAGAAACACTCGCAGAAAATGGCTCTCGGCCGCCACAGCACGGGTCCGACACAGCGCCGCCAT A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr8:80030132..80030259;chr8:80030085..80030275 26863196 MeRIP-seq:(Medium) rs114563553 Functional Loss SNV dbSNP153 33..33 33 - - - 104764 RMVar_ID_104764 Human_SNP_ID_370147056 m1A Human chr8 - 80053401 80053401 80053401 TAGGTAGAAGAAGAAATCCAGACTCTGTCTCAAGTGTTAGCAGCAAAAGAGAAGCATCTAGCAGA TAGGTAGAAGAAGAAATCCAGACTCTGTCTCAGGTGTTAGCAGCAAAAGAGAAGCATCTAGCAGA T C AC036214.3,TPD52 Ensembl:ENSG00000276418,Ensembl:ENSG00000076554 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:80053351..80053484 26863196 MeRIP-seq:(Medium) rs1373929672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_958187,Human_RBP_ID_2057594,Human_RBP_ID_5002648,Human_RBP_ID_7859270,Human_RBP_ID_9405574,Human_RBP_ID_17546673 Human_Splice_Rec_987798,Human_Splice_Rec_987810,Human_Splice_Rec_987818,Human_Splice_Rec_987828,Human_Splice_Rec_987840,Human_Splice_Rec_987852,Human_Splice_Rec_987862,Human_Splice_Rec_987876,Human_Splice_Rec_987884,Human_Splice_Rec_987898,Human_Splice_Rec_987904,Human_Splice_Rec_987918,Human_Splice_Rec_987930,Human_Splice_Rec_987956,Human_Splice_Rec_987966,Human_Splice_Rec_987974,Human_Splice_Rec_987978,Human_Splice_Rec_987982 RMVar_hsa_circ_55323,RMVar_hsa_circ_75154,RMVar_hsa_circ_57255,RMVar_hsa_circ_364989,RMVar_hsa_circ_71974,RMVar_hsa_circ_317869,RMVar_hsa_circ_252816 104765 RMVar_ID_104765 Human_SNP_ID_370149672 m1A Human chr8 - 80064537 80064537 80064537 CTGAGGAAGGAGAAGATGTTGCTGCCACGATCAGTGCCACAGAGACCCTCTCGGAAGAGGAGCAG CTGAGGAAGGAGAAGATGTTGCTGCCACGATCGGTGCCACAGAGACCCTCTCGGAAGAGGAGCAG T C AC036214.3,TPD52 Ensembl:ENSG00000276418,Ensembl:ENSG00000076554 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:80053276..80080381 26863196 MeRIP-seq:(Medium) rs201546255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4991729,Human_RBP_ID_9405575 Human_Splice_Rec_987796,Human_Splice_Rec_987797,Human_Splice_Rec_987808,Human_Splice_Rec_987809,Human_Splice_Rec_987816,Human_Splice_Rec_987817,Human_Splice_Rec_987826,Human_Splice_Rec_987827,Human_Splice_Rec_987838,Human_Splice_Rec_987839,Human_Splice_Rec_987850,Human_Splice_Rec_987851,Human_Splice_Rec_987860,Human_Splice_Rec_987861,Human_Splice_Rec_987874,Human_Splice_Rec_987875,Human_Splice_Rec_987882,Human_Splice_Rec_987883,Human_Splice_Rec_987897,Human_Splice_Rec_987916,Human_Splice_Rec_987917,Human_Splice_Rec_987928,Human_Splice_Rec_987929,Human_Splice_Rec_987954,Human_Splice_Rec_987955,Human_Splice_Rec_987964,Human_Splice_Rec_987965,Human_Splice_Rec_987972,Human_Splice_Rec_987973,Human_Splice_Rec_987977,Human_Splice_Rec_987980,Human_Splice_Rec_987981,Human_Splice_Rec_987984,Human_Splice_Rec_987986 RMVar_hsa_circ_55323,RMVar_hsa_circ_71974,RMVar_hsa_circ_317869,RMVar_hsa_circ_69300,RMVar_hsa_circ_252816,RMVar_hsa_circ_252817 104766 RMVar_ID_104766 Human_SNP_ID_370166137 m1A Human chr8 - 80133455 80133455 80133455 GAACACAAAGAGGAAAGAATATCTGGTTTTGGAGGGAAGAAGGAAAATTCAGTTTTGATTCTGAA GAACACAAAGAGGAAAGAATATCTGGTTTTGGCGGGAAGAAGGAAAATTCAGTTTTGATTCTGAA T G TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:80133450..80133635 26863196 MeRIP-seq:(Medium) rs1246994548 Functional Loss SNV dbSNP153 33..33 33 - - - 104767 RMVar_ID_104767 Human_SNP_ID_370175578 m1A Human chr8 + 80171477 80171477 80171477 TCTCCAGCCCGCCGCCTCGTGTCCTCTGCAGCACCCCCGCCTGCAGCCCGTCCCGGCTCGGATCG TCTCCAGCCCGCCGCCTCGTGTCCTCTGCAGCCCCCCCGCCTGCAGCCCGTCCCGGCTCGGATCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr8:80171308..80171583;chr8:80171351..80171559 26863196 MeRIP-seq:(Medium) rs781464657 Functional Loss SNV dbSNP153 33..33 33 - - - 104768 RMVar_ID_104768 Human_SNP_ID_370252067 m1A Human chr8 - 80486297 80486297 80486297 GAGAGGCACGCTAAACTGCTCGGCTCCGCCACATAACGAAGCGACAATAAAGCCGGCGGAGCGTT GAGAGGCACGCTAAACTGCTCGGCTCCGCCACCTAACGAAGCGACAATAAAGCCGGCGGAGCGTT T G AC009812.1 Ensembl:ENSG00000251867 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:80486251..80486496 26863196 MeRIP-seq:(Medium) rs923062587 Functional Loss SNV dbSNP153 33..33 33 - - - 104769 RMVar_ID_104769 Human_SNP_ID_370252118 m1A Human chr8 - 80486409 80486409 80486409 GCTGCCCCCTCTTTAAAGCCGCGCGCGCACACACCGATCCTCCACACAGATATCCTTCCTCCGCG GCTGCCCCCTCTTTAAAGCCGCGCGCGCACACGCCGATCCTCCACACAGATATCCTTCCTCCGCG T C AC009812.1 Ensembl:ENSG00000251867 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:80486227..80486446 26863196 MeRIP-seq:(Medium) rs559516817 Functional Loss SNV dbSNP153 33..33 33 - - - 104770 RMVar_ID_104770 Human_SNP_ID_370252119 m1A Human chr8 - 80486409 80486409 80486409 GCTGCCCCCTCTTTAAAGCCGCGCGCGCACACACCGATCCTCCACACAGATATCCTTCCTCCGCG GCTGCCCCCTCTTTAAAGCCGCGCGCGCACACCCCGATCCTCCACACAGATATCCTTCCTCCGCG T G AC009812.1 Ensembl:ENSG00000251867 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:80486227..80486446 26863196 MeRIP-seq:(Medium) rs559516817 Functional Loss SNV dbSNP153 33..33 33 - - - 104771 RMVar_ID_104771 Human_SNP_ID_370252235 m1A Human chr8 + 80486612 80486601 80486613 AGAGCGGTCGGAGGCGTCGGCCCGGCAGCGGCAGCGGCAGCGGACGCGTGCAGCAGACCCGGGAG AGAGCGGTCGGAGGCGTCGGCC____________CGGCAGCGGACGCGTGCAGCAGACCCGGGAG CCGGCAGCGGCAG C ZBTB10 Ensembl:ENSG00000205189 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:80486239..80487086 26863196 MeRIP-seq:(Medium) rs537446139 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_4995090 104772 RMVar_ID_104772 Human_SNP_ID_370252236 m1A Human chr8 + 80486612 80486601 80486613 AGAGCGGTCGGAGGCGTCGGCCCGGCAGCGGCAGCGGCAGCGGACGCGTGCAGCAGACCCGGGAG AGAGCGGTCGGAGGCGTCGGCCCGGCAG______CGGCAGCGGACGCGTGCAGCAGACCCGGGAG CCGGCAGCGGCAG CCGGCAG ZBTB10 Ensembl:ENSG00000205189 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:80486239..80487086 26863196 MeRIP-seq:(Medium) rs537446139 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_4995090 104773 RMVar_ID_104773 Human_SNP_ID_370252250 m1A Human chr8 + 80486623 80486623 80486623 AGGCGTCGGCCCGGCAGCGGCAGCGGCAGCGGACGCGTGCAGCAGACCCGGGAGCGAGCGCGAGC AGGCGTCGGCCCGGCAGCGGCAGCGGCAGCGGGCGCGTGCAGCAGACCCGGGAGCGAGCGCGAGC A G ZBTB10 Ensembl:ENSG00000205189 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:80485817..80486895 26863196 MeRIP-seq:(Medium) rs1053870730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995090 104774 RMVar_ID_104774 Human_SNP_ID_370252332 m1A Human chr8 + 80486773 80486773 80486773 AGCGCGCGGGACGCGGCCCGAGGCCGTGCGCGAGCCGGGGCACCGGGCGGCGGCGGCGGCGGCGC AGCGCGCGGGACGCGGCCCGAGGCCGTGCGCGGGCCGGGGCACCGGGCGGCGGCGGCGGCGGCGC A G ZBTB10 Ensembl:ENSG00000205189 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:80486545..80487094 26863196 MeRIP-seq:(Medium) rs1490307494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796798,Human_RBP_ID_4996195,Human_RBP_ID_5534225,Human_RBP_ID_9338298,Human_RBP_ID_18466773,Human_RBP_ID_26795463 104775 RMVar_ID_104775 Human_SNP_ID_370344142 m1A Human chr8 - 80873716 80873714 80873717 CAGGCGGCGGAGGGGGCTCGGGCGTGTGGAGGAGAAGCCCCGAGGGGGCGCGGAGGAGGAGGATG CAGGCGGCGGAGGGGGCTCGGGCGTGTGGAG___AAGCCCCGAGGGGGCGCGGAGGAGGAGGATG TCTC T ZNF704 Ensembl:ENSG00000164684 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:80873571..80874127 26863196 MeRIP-seq:(Medium) rs1381694310 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_19022064,Human_RBP_ID_23088099 104776 RMVar_ID_104776 Human_SNP_ID_370440116 m1A Human chr8 - 81280566 81280566 81280566 CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGAGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGTGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA T A AC009902.2 Ensembl:ENSG00000254027 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81280510..81280625;chr8:81280510..81280635;chr8:81280505..81280642 26863196 MeRIP-seq:(Medium) rs765997771 Functional Loss SNV dbSNP153 33..33 33 - - - 104777 RMVar_ID_104777 Human_SNP_ID_370440117 m1A Human chr8 - 81280566 81280566 81280566 CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGAGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGGGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA T C AC009902.2 Ensembl:ENSG00000254027 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81280510..81280625;chr8:81280510..81280635;chr8:81280505..81280642 26863196 MeRIP-seq:(Medium) rs765997771 Functional Loss SNV dbSNP153 33..33 33 - - - 104778 RMVar_ID_104778 Human_SNP_ID_370440118 m1A Human chr8 - 81280566 81280566 81280566 CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGAGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA CATGGTGGGTGCGGGCGGGCTGGCGTGCAGAGCGGGGTCTGCGTCGGCGTGGCAGCGTGCTGTGA T G AC009902.2 Ensembl:ENSG00000254027 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81280510..81280625;chr8:81280510..81280635;chr8:81280505..81280642 26863196 MeRIP-seq:(Medium) rs765997771 Functional Loss SNV dbSNP153 33..33 33 - - - 104779 RMVar_ID_104779 Human_SNP_ID_370440153 m1A Human chr8 - 81280636 81280636 81280636 CCTTCATGTATTCATCAAAGCCTTTGCTGTCCACCAGGCGCCATCTTCCTTCCAGCTGCTGAACT CCTTCATGTATTCATCAAAGCCTTTGCTGTCCTCCAGGCGCCATCTTCCTTCCAGCTGCTGAACT T A AC009902.2 Ensembl:ENSG00000254027 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:81280535..81280640 26863410 MeRIP-seq:(Medium) rs1311146421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_988241 104780 RMVar_ID_104780 Human_SNP_ID_370498237 m1A Human chr8 - 81522199 81522199 81522199 CATGGCGACCCCGTCCACCTCGCAGGAGCGCCAGGACTACAACCAGGACTCAGAGGCCGCCATCA CATGGCGACCCCGTCCACCTCGCAGGAGCGCCGGGACTACAACCAGGACTCAGAGGCCGCCATCA T C FTH1P11 Ensembl:ENSG00000237264 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:81522149..81522349 26863196 MeRIP-seq:(Medium) rs895310663 Functional Loss SNV dbSNP153 33..33 33 - - - 104781 RMVar_ID_104781 Human_SNP_ID_370533259 m1A Human chr8 + 81674313 81674313 81674313 CTGCTCCATCAGCTGATTCCCTAGTCTCTTGGATTTTTCTTCTTATACCTTCTCATTAAGTTTCT CTGCTCCATCAGCTGATTCCCTAGTCTCTTGGGTTTTTCTTCTTATACCTTCTCATTAAGTTTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:81674262..81674456 26863196 MeRIP-seq:(Medium) rs1011838265 Functional Loss SNV dbSNP153 33..33 33 - - - 104782 RMVar_ID_104782 Human_SNP_ID_370545808 m1A Human chr8 - 81721244 81721243 81721244 GGAGTTGGACATCGGGCAGCACTGCCAGGTGGAGCATTGCCGGCAGCGAGGTGATCCGGGAGCTT GGAGTTGGACATCGGGCAGCACTGCCAGGTGG_GCATTGCCGGCAGCGAGGTGATCCGGGAGCTT CT C ZFAND1 Ensembl:ENSG00000104231 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81721099..81721244;chr8:81721099..81721245 26863196 MeRIP-seq:(Medium) rs1382758836 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4995578,Human_RBP_ID_7860958,Human_RBP_ID_16483442,Human_RBP_ID_24269803 Human_Splice_Rec_988499,Human_Splice_Rec_988513,Human_Splice_Rec_988527,Human_Splice_Rec_988545,Human_Splice_Rec_988585,Human_Splice_Rec_988609,Human_Splice_Rec_988619,Human_Splice_Rec_988651,Human_Splice_Rec_988685,Human_Splice_Rec_988699 104783 RMVar_ID_104783 Human_SNP_ID_370545809 m1A Human chr8 - 81721244 81721244 81721244 GGAGTTGGACATCGGGCAGCACTGCCAGGTGGAGCATTGCCGGCAGCGAGGTGATCCGGGAGCTT GGAGTTGGACATCGGGCAGCACTGCCAGGTGGGGCATTGCCGGCAGCGAGGTGATCCGGGAGCTT T C ZFAND1 Ensembl:ENSG00000104231 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81721099..81721244;chr8:81721099..81721245 26863196 MeRIP-seq:(Medium) rs759922306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995578,Human_RBP_ID_7860958,Human_RBP_ID_16483442,Human_RBP_ID_24269803 Human_Splice_Rec_988499,Human_Splice_Rec_988513,Human_Splice_Rec_988527,Human_Splice_Rec_988545,Human_Splice_Rec_988585,Human_Splice_Rec_988609,Human_Splice_Rec_988619,Human_Splice_Rec_988651,Human_Splice_Rec_988685,Human_Splice_Rec_988699 104784 RMVar_ID_104784 Human_SNP_ID_370545810 m1A Human chr8 - 81721244 81721244 81721244 GGAGTTGGACATCGGGCAGCACTGCCAGGTGGAGCATTGCCGGCAGCGAGGTGATCCGGGAGCTT GGAGTTGGACATCGGGCAGCACTGCCAGGTGGCGCATTGCCGGCAGCGAGGTGATCCGGGAGCTT T G ZFAND1 Ensembl:ENSG00000104231 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:81721099..81721244;chr8:81721099..81721245 26863196 MeRIP-seq:(Medium) rs759922306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995578,Human_RBP_ID_7860958,Human_RBP_ID_16483442,Human_RBP_ID_24269803 Human_Splice_Rec_988499,Human_Splice_Rec_988513,Human_Splice_Rec_988527,Human_Splice_Rec_988545,Human_Splice_Rec_988585,Human_Splice_Rec_988609,Human_Splice_Rec_988619,Human_Splice_Rec_988651,Human_Splice_Rec_988685,Human_Splice_Rec_988699 104785 RMVar_ID_104785 Human_SNP_ID_370548482 m1A Human chr8 + 81732306 81732306 81732306 CCTGGGACCGTCCCTAGTGTGGATAAAAGCCAACTTCCCACAGTCTTTGTCGGTCTTTTCAACTT CCTGGGACCGTCCCTAGTGTGGATAAAAGCCAGCTTCCCACAGTCTTTGTCGGTCTTTTCAACTT A G lnc-CHMP4C-7 RNACentral:URS00008B31BE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:81732255..81732372 26863196 MeRIP-seq:(Medium) rs777251122 Functional Loss SNV dbSNP153 33..33 33 - - - 104786 RMVar_ID_104786 Human_SNP_ID_371410192 m1A Human chr8 - 85107315 85107309 85107315 CTTCGTTTTCCACTTCCGCCTCTGCCGCCACCACCGCCGCCGCCGCCTCCATAGCACTGGCGACG CTTCGTTTTCCACTTCCGCCTCTGCCGCCACC______GCCGCCGCCTCCATAGCACTGGCGACG CGGCGGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:85107269..85107353 26863196 MeRIP-seq:(Medium) rs773342260 Functional Loss DEL dbSNP153 33..38 33 - - - 104787 RMVar_ID_104787 Human_SNP_ID_371410200 m1A Human chr8 - 85107315 85107315 85107315 CTTCGTTTTCCACTTCCGCCTCTGCCGCCACCACCGCCGCCGCCGCCTCCATAGCACTGGCGACG CTTCGTTTTCCACTTCCGCCTCTGCCGCCACCGCCGCCGCCGCCGCCTCCATAGCACTGGCGACG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:85107269..85107353 26863196 MeRIP-seq:(Medium) rs749120809 Functional Loss SNV dbSNP153 33..33 33 - - - 104788 RMVar_ID_104788 Human_SNP_ID_371412035 m1A Human chr8 + 85115183 85115183 85115183 GCAAGAACATATTTGGTGAACCAGTAAATTTGACAGAAATAAATTCATCACAGCTGCAGTGCCTA GCAAGAACATATTTGGTGAACCAGTAAATTTGGCAGAAATAAATTCATCACAGCTGCAGTGCCTA A G LRRCC1 Ensembl:ENSG00000133739 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3736038 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_989160,Human_Splice_Rec_989161,Human_Splice_Rec_989188,Human_Splice_Rec_989189,Human_Splice_Rec_989218,Human_Splice_Rec_989219,Human_Splice_Rec_989252,Human_Splice_Rec_989253 GWAS_ID_13697,GWAS_ID_13698,GWAS_ID_13699,GWAS_ID_13700 RMVar_hsa_circ_10267,RMVar_hsa_circ_296745,RMVar_hsa_circ_333387,RMVar_hsa_circ_346496,RMVar_hsa_circ_305075,RMVar_hsa_circ_284787,RMVar_hsa_circ_252878,RMVar_hsa_circ_252880,RMVar_hsa_circ_252881,RMVar_hsa_circ_252882,RMVar_hsa_circ_252879,RMVar_hsa_circ_18976,RMVar_hsa_circ_252883,RMVar_hsa_circ_102791 104789 RMVar_ID_104789 Human_SNP_ID_371426675 m1A Human chr8 - 85177279 85177279 85177279 AGCGGTAGTGCGGGTCGCTGGCTGCTGCAAACAACAGGTGTGCGGCGCCCACGGGAGTCTGGGCC AGCGGTAGTGCGGGTCGCTGGCTGCTGCAAACGACAGGTGTGCGGCGCCCACGGGAGTCTGGGCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:85177192..85177295 26863410 MeRIP-seq:(Medium) rs1396104384 Functional Loss SNV dbSNP153 33..33 33 - - - 104790 RMVar_ID_104790 Human_SNP_ID_371437255 m1A Human chr8 + 85220271 85220271 85220271 AATCCAACCCCGACCCCTGCAAACTTCACGCCAGCCCTCCAGAAAACTTAATTTATTAAACTCTC AATCCAACCCCGACCCCTGCAAACTTCACGCCTGCCCTCCAGAAAACTTAATTTATTAAACTCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:85220267..85220339 26863196 MeRIP-seq:(Medium) rs558798071 Functional Loss SNV dbSNP153 33..33 33 - - - 104791 RMVar_ID_104791 Human_SNP_ID_371498507 m1A Human chr8 + 85480676 85480676 85480676 TATCAATGTTTTATTGTGTCTTTTAGGTGTTGAAATTCCGTAAACTTAACTTCAATGGGGAGGGT TATCAATGTTTTATTGTGTCTTTTAGGTGTTGCAATTCCGTAAACTTAACTTCAATGGGGAGGGT A C CA2 Ensembl:ENSG00000104267 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1364755620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_705023,Human_RBP_ID_17546773,Human_RBP_ID_18123040,Human_RBP_ID_27127385 Human_Splice_Rec_989780,Human_Splice_Rec_989798 104792 RMVar_ID_104792 Human_SNP_ID_371688194 m1A Human chr8 - 86342587 86342587 86342587 GCGCCTCCCCGCCGGCCCCGGCACCGCGCGCTACGCCGCGGCCGCCCAAAGCCTCCAACTCCGGA GCGCCTCCCCGCCGGCCCCGGCACCGCGCGCTGCGCCGCGGCCGCCCAAAGCCTCCAACTCCGGA T C AC103760.1 Ensembl:ENSG00000254231 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:86342536..86342695 26863196 MeRIP-seq:(Medium) rs1197182407 Functional Loss SNV dbSNP153 33..33 33 - - - 104793 RMVar_ID_104793 Human_SNP_ID_371688276 m1A Human chr8 - 86342751 86342751 86342751 GCCCAGGCCGCCAGCAGCCACTCGGAACCCGCACGCGGAGCTCGCCGACACCCGACCCTCCCCCC GCCCAGGCCGCCAGCAGCCACTCGGAACCCGCTCGCGGAGCTCGCCGACACCCGACCCTCCCCCC T A AC103760.1 Ensembl:ENSG00000254231 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:86342701..86374093 26863196 MeRIP-seq:(Medium) rs1413729472 Functional Loss SNV dbSNP153 33..33 33 - - - 104794 RMVar_ID_104794 Human_SNP_ID_371695828 m1A Human chr8 + 86373971 86373971 86373971 CTTCTTAGTTGATTTAAACAAGTAGTTTTAATATCTTGAAAATTACAAACTCTTATCTAACACAT CTTCTTAGTTGATTTAAACAAGTAGTTTTAATGTCTTGAAAATTACAAACTCTTATCTAACACAT A G WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:86373968..86374059 26863196 MeRIP-seq:(Medium) rs766932058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1336805 RMVar_hsa_circ_127896,RMVar_hsa_circ_93488,RMVar_hsa_circ_273811,RMVar_hsa_circ_298904,RMVar_hsa_circ_252892,RMVar_hsa_circ_309466,RMVar_hsa_circ_275801,RMVar_hsa_circ_94832,RMVar_hsa_circ_252894,RMVar_hsa_circ_64317,RMVar_hsa_circ_75378,RMVar_hsa_circ_252895,RMVar_hsa_circ_252896,RMVar_hsa_circ_252893 104795 RMVar_ID_104795 Human_SNP_ID_372612913 m1A Human chr8 + 89902635 89902635 89902635 GAAGCCGCTATCTGGAGGCGGACTCCGGCGCCACAGAGCCGGGGCAGCCGCGGCAACGGCGAGGC GAAGCCGCTATCTGGAGGCGGACTCCGGCGCCGCAGAGCCGGGGCAGCCGCGGCAACGGCGAGGC A G OSGIN2 Ensembl:ENSG00000164823 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:89902591..89902679 26863196 MeRIP-seq:(Medium) rs1234336307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995590,Human_RBP_ID_5430668,Human_RBP_ID_8923568 104796 RMVar_ID_104796 Human_SNP_ID_372612930 m1A Human chr8 + 89902675 89902675 89902675 GGGGCAGCCGCGGCAACGGCGAGGCGCGAGGCAGGGGCGCCCGGCAGACCCCGCGACCCCGAGCC GGGGCAGCCGCGGCAACGGCGAGGCGCGAGGCCGGGGCGCCCGGCAGACCCCGCGACCCCGAGCC A C OSGIN2 Ensembl:ENSG00000164823 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:89902576..89902725 26863410 MeRIP-seq:(Medium) rs977440876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995590,Human_RBP_ID_8923568 104797 RMVar_ID_104797 Human_SNP_ID_372633860 m1A Human chr8 + 89984616 89984592 89984617 GGCCGACGTGCAACCGCGTAACCGGGGCTGCTAGACGAGCGCGGATACGGCGCCTGCGGTCGGCA GGCCGACGT_________________________ACGAGCGCGGATACGGCGCCTGCGGTCGGCA TGCAACCGCGTAACCGGGGCTGCTAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:89984566..89984634 26863196 MeRIP-seq:(Medium) rs1563589177 Functional Loss DEL dbSNP153 10..34 33 - - - 104798 RMVar_ID_104798 Human_SNP_ID_546787483 m1A Human chr14 + 19075237 19075237 19075237 TAGATTCAGTGTCAGCTATGACAATTGAAAATAAGCTGTTTTGTGATTTAAAGGTTTAAATTTCT TAGATTCAGTGTCAGCTATGACAATTGAAAATGAGCTGTTTTGTGATTTAAAGGTTTAAATTTCT A G AL589182.3,DUXAP9 Ensembl:ENSG00000286614,Ensembl:ENSG00000225210 Pseudogene,Pseudogene exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs768451165 Functional Loss SNV dbSNP153 33..33 33 - - - 104799 RMVar_ID_104799 Human_SNP_ID_546792859 m1A Human chr14 + 19096651 19096647 19096651 AGAGGGTGAGAGTGTGTGCGTGTGTTAGTGTGAGTGTGTGTGTATGTAAGGAGCAGGAGTGACTG AGAGGGTGAGAGTGTGTGCGTGTGTTAGT____GTGTGTGTGTATGTAAGGAGCAGGAGTGACTG TGTGA T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:19096615..19096696;chr14:19096601..19096700;chr14:19096592..19096803;chr14:19096614..19096796;chr14:19096554..19096765 26863196 MeRIP-seq:(Medium) rs140164336 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_196981,Human_RBP_ID_1065666,Human_RBP_ID_3469235,Human_RBP_ID_5236020,Human_RBP_ID_5645767,Human_RBP_ID_8078567,Human_RBP_ID_9417703,Human_RBP_ID_17248723,Human_RBP_ID_17669301,Human_RBP_ID_18936572,Human_RBP_ID_23643963,Human_RBP_ID_26431546 104800 RMVar_ID_104800 Human_SNP_ID_546792860 m1A Human chr14 + 19096651 19096649 19096651 AGAGGGTGAGAGTGTGTGCGTGTGTTAGTGTGAGTGTGTGTGTATGTAAGGAGCAGGAGTGACTG AGAGGGTGAGAGTGTGTGCGTGTGTTAGTGT__GTGTGTGTGTATGTAAGGAGCAGGAGTGACTG TGA T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:19096615..19096696;chr14:19096601..19096700;chr14:19096592..19096803;chr14:19096614..19096796;chr14:19096554..19096765 26863196 MeRIP-seq:(Medium) rs147794535 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_196981,Human_RBP_ID_1065666,Human_RBP_ID_3469235,Human_RBP_ID_5236020,Human_RBP_ID_5645767,Human_RBP_ID_8078567,Human_RBP_ID_9417703,Human_RBP_ID_17248723,Human_RBP_ID_17669301,Human_RBP_ID_18936572,Human_RBP_ID_23643963,Human_RBP_ID_26431546 104801 RMVar_ID_104801 Human_SNP_ID_546792863 m1A Human chr14 + 19096651 19096651 19096651 AGAGGGTGAGAGTGTGTGCGTGTGTTAGTGTGAGTGTGTGTGTATGTAAGGAGCAGGAGTGACTG AGAGGGTGAGAGTGTGTGCGTGTGTTAGTGTGTGTGTGTGTGTATGTAAGGAGCAGGAGTGACTG A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr14:19096615..19096696;chr14:19096601..19096700;chr14:19096592..19096803;chr14:19096614..19096796;chr14:19096554..19096765 26863196 MeRIP-seq:(Medium) rs1200140066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_196981,Human_RBP_ID_1065666,Human_RBP_ID_3469235,Human_RBP_ID_5236020,Human_RBP_ID_5645767,Human_RBP_ID_8078567,Human_RBP_ID_9417703,Human_RBP_ID_17248723,Human_RBP_ID_17669301,Human_RBP_ID_18936572,Human_RBP_ID_23643963,Human_RBP_ID_26431546 104802 RMVar_ID_104802 Human_SNP_ID_546793413 m1A Human chr14 + 19097602 19097602 19097602 CCCGAGTCGCACACGCCCCGCAAGCCCTGGCCACCGACCCGGAGGGAACGCCCTGGGCTACGGTC CCCGAGTCGCACACGCCCCGCAAGCCCTGGCCCCCGACCCGGAGGGAACGCCCTGGGCTACGGTC A C DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:19097501..19097625 26863410 MeRIP-seq:(Medium) rs1264077895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2431802,Human_RBP_ID_8725672,Human_RBP_ID_22414954,Human_RBP_ID_22711247,Human_RBP_ID_23118250 104803 RMVar_ID_104803 Human_SNP_ID_546793466 m1A Human chr14 + 19097699 19097699 19097699 CCGACTCCAAAGCCGCATCTCCAGCTTTGTTCATGGGTCCGGGAAGCAGAGGCCGCCGCCGGCCA CCGACTCCAAAGCCGCATCTCCAGCTTTGTTCGTGGGTCCGGGAAGCAGAGGCCGCCGCCGGCCA A G DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200585687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8941146 104804 RMVar_ID_104804 Human_SNP_ID_546793659 m1A Human chr14 + 19097956 19097956 19097956 CAGGCCTGCGGCTCCGGCCACGGGGCGGGGGCAGAAAAACGACCCCGGCGCTGTCCGGGCATCCA CAGGCCTGCGGCTCCGGCCACGGGGCGGGGGCTGAAAAACGACCCCGGCGCTGTCCGGGCATCCA A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:19097933..19098018 26863410 MeRIP-seq:(Medium) rs1221484440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3467648,Human_RBP_ID_5176818,Human_RBP_ID_5236021,Human_RBP_ID_5315815,Human_RBP_ID_8725673,Human_RBP_ID_9417705,Human_RBP_ID_18160818,Human_RBP_ID_18480383,Human_RBP_ID_22369979,Human_RBP_ID_22696453,Human_RBP_ID_22711176,Human_RBP_ID_22737444,Human_RBP_ID_26778055 104805 RMVar_ID_104805 Human_SNP_ID_546793925 m1A Human chr14 + 19098431 19098431 19098431 CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGAAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGTAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs865892571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17249243,Human_RBP_ID_17673155 104806 RMVar_ID_104806 Human_SNP_ID_546794216 m1A Human chr14 + 19098957 19098957 19098957 GACGGGGCGATTGGGAGGGGGTTCTGGAGCTCACGCCTGGGGTCGGCCCGGCGGGGGTGACCCCG GACGGGGCGATTGGGAGGGGGTTCTGGAGCTCGCGCCTGGGGTCGGCCCGGCGGGGGTGACCCCG A G DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:19098910..19098994 26863196 MeRIP-seq:(Medium) rs1422854779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5140712,Human_RBP_ID_5236120,Human_RBP_ID_8078569,Human_RBP_ID_9323712,Human_RBP_ID_18480384,Human_RBP_ID_22711251,Human_RBP_ID_26778056,Human_RBP_ID_26921761 104807 RMVar_ID_104807 Human_SNP_ID_546794217 m1A Human chr14 + 19098957 19098957 19098957 GACGGGGCGATTGGGAGGGGGTTCTGGAGCTCACGCCTGGGGTCGGCCCGGCGGGGGTGACCCCG GACGGGGCGATTGGGAGGGGGTTCTGGAGCTCTCGCCTGGGGTCGGCCCGGCGGGGGTGACCCCG A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:19098910..19098994 26863196 MeRIP-seq:(Medium) rs1422854779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5140712,Human_RBP_ID_5236120,Human_RBP_ID_8078569,Human_RBP_ID_9323712,Human_RBP_ID_18480384,Human_RBP_ID_22711251,Human_RBP_ID_26778056,Human_RBP_ID_26921761 104808 RMVar_ID_104808 Human_SNP_ID_546794262 m1A Human chr14 - 19099002 19099002 19099002 CTGCCCCGGCGGGAACCACCTGTTCTCCTTGCACCGGCGAGGGCGCGGGGTCACCCCCGCCGGGC CTGCCCCGGCGGGAACCACCTGTTCTCCTTGCGCCGGCGAGGGCGCGGGGTCACCCCCGCCGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:19098959..19099042 26863196 MeRIP-seq:(Medium) rs1306461004 Functional Loss SNV dbSNP153 33..33 33 - - - 104809 RMVar_ID_104809 Human_SNP_ID_546796063 m1A Human chr14 + 19104747 19104747 19104747 CATGGTGAATACAATCAAGTTCAGTGTATTTGATAATATCAATTTGGGCCCCAAATCTCTCTCAC CATGGTGAATACAATCAAGTTCAGTGTATTTGTTAATATCAATTTGGGCCCCAAATCTCTCTCAC A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1555347817 Functional Loss SNV dbSNP153 33..33 33 - - - 104810 RMVar_ID_104810 Human_SNP_ID_546860175 m1A Human chr14 - 19301593 19301593 19301593 CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGAAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGTAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG T A AL589743.1 Ensembl:ENSG00000244306 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78811920 Functional Loss SNV dbSNP153 33..33 33 - - - 104811 RMVar_ID_104811 Human_SNP_ID_547129657 m1A Human chr14 - 20305910 20305910 20305910 GGGAGATGATGGCTGATGAAGAGGAAGAAGTCAAGCCGATCTTGCAGAAATTGCAGGTGGGGCCG GGGAGATGATGGCTGATGAAGAGGAAGAAGTCCAGCCGATCTTGCAGAAATTGCAGGTGGGGCCG T G TTC5 Ensembl:ENSG00000136319 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:20305839..20305927;chr14:20305829..20305926 26863196 MeRIP-seq:(Medium) rs747559760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1490264,Human_RBP_ID_1815903,Human_RBP_ID_4310759,Human_RBP_ID_18980000,Human_RBP_ID_19063529 Human_Splice_Rec_1487371,Human_Splice_Rec_1487389,Human_Splice_Rec_1487407,Human_Splice_Rec_1487423 104812 RMVar_ID_104812 Human_SNP_ID_547129661 m1A Human chr14 + 20305912 20305912 20305912 GCCCCACCTGCAATTTCTGCAAGATCGGCTTGACTTCTTCCTCTTCATCAGCCATCATCTCCCGG GCCCCACCTGCAATTTCTGCAAGATCGGCTTGGCTTCTTCCTCTTCATCAGCCATCATCTCCCGG A G AL356019.1 Ensembl:ENSG00000258459 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:20305845..20305950 26863196 MeRIP-seq:(Medium) rs1461110231 Functional Loss SNV dbSNP153 33..33 33 - - - 104813 RMVar_ID_104813 Human_SNP_ID_547136206 m1A Human chr14 + 20329232 20329232 20329232 TTATCTTGATCAAAATTCAAGTACCAGGCTTTAGGTACCATCAGCCTTTAACCCTTTCTGTTGAG TTATCTTGATCAAAATTCAAGTACCAGGCTTTTGGTACCATCAGCCTTTAACCCTTTCTGTTGAG A T lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20325626..20329317 32194978 MeRIP-seq:(Medium) rs115705164 Functional Loss SNV dbSNP153 33..33 33 - - - 104814 RMVar_ID_104814 Human_SNP_ID_547139774 m1A Human chr14 + 20343189 20343189 20343189 GTGAGTCTGTTCCAAGCTCCGGCAAAGGAGGCATCCGCCGGGCCCCTCCCCGAAGGGCGGGGTCC GTGAGTCTGTTCCAAGCTCCGGCAAAGGAGGCCTCCGCCGGGCCCCTCCCCGAAGGGCGGGGTCC A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20343145..20343342 32194978 MeRIP-seq:(Medium) rs1256704262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165052,RMVar_hsa_circ_165053,RMVar_hsa_circ_111764,RMVar_hsa_circ_165070,RMVar_hsa_circ_165069 104815 RMVar_ID_104815 Human_SNP_ID_547139903 m1A Human chr14 - 20343305 20343305 20343305 GAAGGTCTGAGACTAGGGCCAGAGGCGGCCCTAACAGGGCTCTCCCTGAGCTTCGGGGAGGTGAG GAAGGTCTGAGACTAGGGCCAGAGGCGGCCCTCACAGGGCTCTCCCTGAGCTTCGGGGAGGTGAG T G AL355075.4,RPPH1 Ensembl:ENSG00000259001,Ensembl:ENSG00000277209 lincRNA,Other exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:20343259..20343351 26863196 MeRIP-seq:(Medium) rs967611171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231451,Human_RBP_ID_269584,Human_RBP_ID_442654,Human_RBP_ID_757676,Human_RBP_ID_812995,Human_RBP_ID_882516,Human_RBP_ID_1063968,Human_RBP_ID_1085865,Human_RBP_ID_1274177,Human_RBP_ID_1490345,Human_RBP_ID_1815947,Human_RBP_ID_2408015,Human_RBP_ID_3443562,Human_RBP_ID_4286093,Human_RBP_ID_5087655,Human_RBP_ID_5175882,Human_RBP_ID_5274350,Human_RBP_ID_5563029,Human_RBP_ID_5646063,Human_RBP_ID_8182472,Human_RBP_ID_8250047,Human_RBP_ID_8401080,Human_RBP_ID_17686952,Human_RBP_ID_18199482,Human_RBP_ID_18206825,Human_RBP_ID_18435645,Human_RBP_ID_19919918,Human_RBP_ID_22495231,Human_RBP_ID_22797280,Human_RBP_ID_23126662,Human_RBP_ID_23306712,Human_RBP_ID_23614972,Human_RBP_ID_26427699,Human_RBP_ID_26748369,Human_RBP_ID_27155317,Human_RBP_ID_27430160 Human_miRNA_ID_2008827,Human_miRNA_ID_2008828,Human_miRNA_ID_2008829,Human_miRNA_ID_2008830,Human_miRNA_ID_2008831,Human_miRNA_ID_2008832,Human_miRNA_ID_3150514 RMVar_hsa_circ_340724,RMVar_hsa_circ_165062,RMVar_hsa_circ_165054,RMVar_hsa_circ_165063,RMVar_hsa_circ_165066,RMVar_hsa_circ_376994,RMVar_hsa_circ_165067,RMVar_hsa_circ_165065,RMVar_hsa_circ_165071,RMVar_hsa_circ_267275,RMVar_hsa_circ_165076,RMVar_hsa_circ_165073,RMVar_hsa_circ_379026,RMVar_hsa_circ_377258,RMVar_hsa_circ_165074,RMVar_hsa_circ_165078,RMVar_hsa_circ_376841,RMVar_hsa_circ_379044,RMVar_hsa_circ_379090,RMVar_hsa_circ_377801,RMVar_hsa_circ_165079,RMVar_hsa_circ_165077 104816 RMVar_ID_104816 Human_SNP_ID_547139912 m1A Human chr14 - 20343315 20343315 20343315 TGTCCCTTGGGAAGGTCTGAGACTAGGGCCAGAGGCGGCCCTAACAGGGCTCTCCCTGAGCTTCG TGTCCCTTGGGAAGGTCTGAGACTAGGGCCAGGGGCGGCCCTAACAGGGCTCTCCCTGAGCTTCG T C AL355075.4,RPPH1 Ensembl:ENSG00000259001,Ensembl:ENSG00000277209 lincRNA,Other exon,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:20343105..20343384 26863196 MeRIP-seq:(Medium) rs555672271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231451,Human_RBP_ID_269584,Human_RBP_ID_442654,Human_RBP_ID_757676,Human_RBP_ID_812995,Human_RBP_ID_882516,Human_RBP_ID_1063968,Human_RBP_ID_1085865,Human_RBP_ID_1274177,Human_RBP_ID_1490345,Human_RBP_ID_1815947,Human_RBP_ID_2408015,Human_RBP_ID_3443563,Human_RBP_ID_4286093,Human_RBP_ID_5087655,Human_RBP_ID_5175882,Human_RBP_ID_5274350,Human_RBP_ID_5563029,Human_RBP_ID_5646063,Human_RBP_ID_6330182,Human_RBP_ID_8182472,Human_RBP_ID_8401081,Human_RBP_ID_12290544,Human_RBP_ID_17686952,Human_RBP_ID_18199482,Human_RBP_ID_18206825,Human_RBP_ID_19919918,Human_RBP_ID_22495231,Human_RBP_ID_22797280,Human_RBP_ID_23126662,Human_RBP_ID_23306712,Human_RBP_ID_23614972,Human_RBP_ID_26427699,Human_RBP_ID_26748369,Human_RBP_ID_27430160 Human_miRNA_ID_2008827,Human_miRNA_ID_2008828,Human_miRNA_ID_2008829,Human_miRNA_ID_2008830,Human_miRNA_ID_2008831,Human_miRNA_ID_2008832,Human_miRNA_ID_3150514 RMVar_hsa_circ_340724,RMVar_hsa_circ_165062,RMVar_hsa_circ_165063,RMVar_hsa_circ_165066,RMVar_hsa_circ_376994,RMVar_hsa_circ_165067,RMVar_hsa_circ_165065,RMVar_hsa_circ_165071,RMVar_hsa_circ_267275,RMVar_hsa_circ_165076,RMVar_hsa_circ_165073,RMVar_hsa_circ_379026,RMVar_hsa_circ_377258,RMVar_hsa_circ_165074,RMVar_hsa_circ_165078,RMVar_hsa_circ_376841,RMVar_hsa_circ_379044,RMVar_hsa_circ_379090,RMVar_hsa_circ_377801,RMVar_hsa_circ_165079,RMVar_hsa_circ_165077 104817 RMVar_ID_104817 Human_SNP_ID_547139913 m1A Human chr14 - 20343315 20343315 20343315 TGTCCCTTGGGAAGGTCTGAGACTAGGGCCAGAGGCGGCCCTAACAGGGCTCTCCCTGAGCTTCG TGTCCCTTGGGAAGGTCTGAGACTAGGGCCAGCGGCGGCCCTAACAGGGCTCTCCCTGAGCTTCG T G AL355075.4,RPPH1 Ensembl:ENSG00000259001,Ensembl:ENSG00000277209 lincRNA,Other exon,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:20343105..20343384 26863196 MeRIP-seq:(Medium) rs555672271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231451,Human_RBP_ID_269584,Human_RBP_ID_442654,Human_RBP_ID_757676,Human_RBP_ID_812995,Human_RBP_ID_882516,Human_RBP_ID_1063968,Human_RBP_ID_1085865,Human_RBP_ID_1274177,Human_RBP_ID_1490345,Human_RBP_ID_1815947,Human_RBP_ID_2408015,Human_RBP_ID_3443563,Human_RBP_ID_4286093,Human_RBP_ID_5087655,Human_RBP_ID_5175882,Human_RBP_ID_5274350,Human_RBP_ID_5563029,Human_RBP_ID_5646063,Human_RBP_ID_6330182,Human_RBP_ID_8182472,Human_RBP_ID_8401081,Human_RBP_ID_12290544,Human_RBP_ID_17686952,Human_RBP_ID_18199482,Human_RBP_ID_18206825,Human_RBP_ID_19919918,Human_RBP_ID_22495231,Human_RBP_ID_22797280,Human_RBP_ID_23126662,Human_RBP_ID_23306712,Human_RBP_ID_23614972,Human_RBP_ID_26427699,Human_RBP_ID_26748369,Human_RBP_ID_27430160 Human_miRNA_ID_2008827,Human_miRNA_ID_2008828,Human_miRNA_ID_2008829,Human_miRNA_ID_2008830,Human_miRNA_ID_2008831,Human_miRNA_ID_2008832,Human_miRNA_ID_3150514 RMVar_hsa_circ_340724,RMVar_hsa_circ_165062,RMVar_hsa_circ_165063,RMVar_hsa_circ_165066,RMVar_hsa_circ_376994,RMVar_hsa_circ_165067,RMVar_hsa_circ_165065,RMVar_hsa_circ_165071,RMVar_hsa_circ_267275,RMVar_hsa_circ_165076,RMVar_hsa_circ_165073,RMVar_hsa_circ_379026,RMVar_hsa_circ_377258,RMVar_hsa_circ_165074,RMVar_hsa_circ_165078,RMVar_hsa_circ_376841,RMVar_hsa_circ_379044,RMVar_hsa_circ_379090,RMVar_hsa_circ_377801,RMVar_hsa_circ_165079,RMVar_hsa_circ_165077 104818 RMVar_ID_104818 Human_SNP_ID_547139963 m1A Human chr14 - 20343359 20343359 20343359 TCAGTGGGGCCACGAGCTGAGTGCGTCCTGTCACTCCACTCCCATGTCCCTTGGGAAGGTCTGAG TCAGTGGGGCCACGAGCTGAGTGCGTCCTGTCGCTCCACTCCCATGTCCCTTGGGAAGGTCTGAG T C AL355075.4,RPPH1 Ensembl:ENSG00000259001,Ensembl:ENSG00000277209 lincRNA,Other exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr14:20343130..20343390;chr14:20343156..20343362;chr14:20343174..20343380 26863196 MeRIP-seq:(Medium) rs967518111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231451,Human_RBP_ID_269585,Human_RBP_ID_442656,Human_RBP_ID_757676,Human_RBP_ID_812995,Human_RBP_ID_882516,Human_RBP_ID_997756,Human_RBP_ID_1063968,Human_RBP_ID_1085865,Human_RBP_ID_1129654,Human_RBP_ID_1171341,Human_RBP_ID_1274178,Human_RBP_ID_1490345,Human_RBP_ID_1815948,Human_RBP_ID_2408017,Human_RBP_ID_3443563,Human_RBP_ID_4286093,Human_RBP_ID_5095569,Human_RBP_ID_5287289,Human_RBP_ID_5418001,Human_RBP_ID_5493301,Human_RBP_ID_5564795,Human_RBP_ID_6330182,Human_RBP_ID_8250049,Human_RBP_ID_8401082,Human_RBP_ID_8793447,Human_RBP_ID_9039850,Human_RBP_ID_9281506,Human_RBP_ID_9758878,Human_RBP_ID_12290549,Human_RBP_ID_16996280,Human_RBP_ID_17478481,Human_RBP_ID_17686954,Human_RBP_ID_17845830,Human_RBP_ID_18199482,Human_RBP_ID_18206825,Human_RBP_ID_18435646,Human_RBP_ID_18512009,Human_RBP_ID_18528218,Human_RBP_ID_18647130,Human_RBP_ID_19909180,Human_RBP_ID_22797280,Human_RBP_ID_23126663,Human_RBP_ID_23160561,Human_RBP_ID_23614972,Human_RBP_ID_24410182,Human_RBP_ID_24470905,Human_RBP_ID_26427699,Human_RBP_ID_26748369,Human_RBP_ID_27430160,Human_RBP_ID_27558823 Human_miRNA_ID_2877642,Human_miRNA_ID_2877643,Human_miRNA_ID_2877644,Human_miRNA_ID_2877645,Human_miRNA_ID_2877646,Human_miRNA_ID_2877647,Human_miRNA_ID_2877648,Human_miRNA_ID_2877649,Human_miRNA_ID_3201773 RMVar_hsa_circ_340724,RMVar_hsa_circ_165063,RMVar_hsa_circ_165066,RMVar_hsa_circ_376994,RMVar_hsa_circ_165065,RMVar_hsa_circ_165071,RMVar_hsa_circ_165073,RMVar_hsa_circ_379026,RMVar_hsa_circ_165078,RMVar_hsa_circ_379044,RMVar_hsa_circ_379090,RMVar_hsa_circ_377801,RMVar_hsa_circ_165079,RMVar_hsa_circ_165077 104819 RMVar_ID_104819 Human_SNP_ID_547140223 m1A Human chr14 + 20343666 20343664 20343666 CGAATTCCATGGCGGCGCGGCGGCGACGGAGCACCGGCGGCGGCAGGGCGAGAGGTTCGGAGCTC CGAATTCCATGGCGGCGCGGCGGCGACGGAG__CCGGCGGCGGCAGGGCGAGAGGTTCGGAGCTC GCA G PARP2 Ensembl:ENSG00000129484 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:20343626..20343735 26863196 MeRIP-seq:(Medium) rs1566415056 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_231716 Human_Splice_Rec_1487575,Human_Splice_Rec_1487605,Human_Splice_Rec_1487635,Human_Splice_Rec_1487647 RMVar_hsa_circ_165080 104820 RMVar_ID_104820 Human_SNP_ID_547140240 m1A Human chr14 + 20343678 20343678 20343678 CGGCGCGGCGGCGACGGAGCACCGGCGGCGGCAGGGCGAGAGGTTCGGAGCTCAATATCGCGGGA CGGCGCGGCGGCGACGGAGCACCGGCGGCGGCGGGGCGAGAGGTTCGGAGCTCAATATCGCGGGA A G PARP2 Ensembl:ENSG00000129484 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:20343625..20343726;chr14:20343624..20343752 26863196 MeRIP-seq:(Medium) rs1157146586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231716 Human_Splice_Rec_1487575,Human_Splice_Rec_1487605,Human_Splice_Rec_1487635,Human_Splice_Rec_1487647 RMVar_hsa_circ_165080 104821 RMVar_ID_104821 Human_SNP_ID_547140248 m1A Human chr14 + 20343686 20343686 20343686 CGGCGACGGAGCACCGGCGGCGGCAGGGCGAGAGGTTCGGAGCTCAATATCGCGGGACGGCATGC CGGCGACGGAGCACCGGCGGCGGCAGGGCGAGGGGTTCGGAGCTCAATATCGCGGGACGGCATGC A G PARP2 Ensembl:ENSG00000129484 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr14:20343626..20343738;chr14:20343626..20343749 26863410,26863196 MeRIP-seq:(Medium) rs776404988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231716 Human_Splice_Rec_1487575,Human_Splice_Rec_1487605,Human_Splice_Rec_1487635,Human_Splice_Rec_1487647 RMVar_hsa_circ_165080 104822 RMVar_ID_104822 Human_SNP_ID_547146527 m1A Human chr14 - 20367031 20367031 20367031 TATTTCTAAAATTCAATCATATGGAAGAATCTATTGAGCAGGTTAGCCTTTGCTTAACTTTCCTC TATTTCTAAAATTCAATCATATGGAAGAATCTGTTGAGCAGGTTAGCCTTTGCTTAACTTTCCTC T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1403881819 Functional Loss SNV dbSNP153 33..33 33 - - - 104823 RMVar_ID_104823 Human_SNP_ID_547169907 m1A Human chr14 + 20447904 20447904 20447904 AGGAAAGAGGAACACTTTTCAATAATACATACACCCCACTCCTCCCACAATGAGGGCCTCCTGGG AGGAAAGAGGAACACTTTTCAATAATACATACGCCCCACTCCTCCCACAATGAGGGCCTCCTGGG A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20447901..20447975 32194978 MeRIP-seq:(Medium) rs1474209777 Functional Loss SNV dbSNP153 33..33 33 - - - 104824 RMVar_ID_104824 Human_SNP_ID_547172214 m1A Human chr14 + 20455821 20455821 20455821 CTCATTTTTGCAGGGGTTTGTGAAGAAGTCGCAGGAACCGTAGGCTTTCGTTGGGTCTATAGTTA CTCATTTTTGCAGGGGTTTGTGAAGAAGTCGCGGGAACCGTAGGCTTTCGTTGGGTCTATAGTTA A G APEX1 Ensembl:ENSG00000100823 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20455817..20456055 26863196 MeRIP-seq:(Medium) rs773103260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5352588,Human_RBP_ID_12290872,Human_RBP_ID_25123807 Human_Splice_Rec_1488352,Human_Splice_Rec_1488408,Human_Splice_Rec_1488424 104825 RMVar_ID_104825 Human_SNP_ID_547172324 m1A Human chr14 - 20456103 20456103 20456103 TAAAAAATGTCTCTTTCCCTCAAATTCCACTCACATCTAATCCTTTCTTCTTAATCCAGGCTCGA TAAAAAATGTCTCTTTCCCTCAAATTCCACTCGCATCTAATCCTTTCTTCTTAATCCAGGCTCGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:20455848..20456750;chr14:20456101..20456125 26863196 MeRIP-seq:(Medium) rs1384813722 Functional Loss SNV dbSNP153 33..33 33 - - - 104826 RMVar_ID_104826 Human_SNP_ID_547172503 m1A Human chr14 - 20456653 20456649 20456653 GGCTTCTTCCTTTACCCACTGTAAGTGAAAAGAAAGGTGGAAAACGTATTATCAATTCAGCAGAA GGCTTCTTCCTTTACCCACTGTAAGTGAAAAG____GTGGAAAACGTATTATCAATTCAGCAGAA CCTTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20456651..20456700 26863196 MeRIP-seq:(Medium) rs752680733 Functional Loss DEL dbSNP153 33..36 33 - - - 104827 RMVar_ID_104827 Human_SNP_ID_547172505 m1A Human chr14 - 20456653 20456653 20456653 GGCTTCTTCCTTTACCCACTGTAAGTGAAAAGAAAGGTGGAAAACGTATTATCAATTCAGCAGAA GGCTTCTTCCTTTACCCACTGTAAGTGAAAAGGAAGGTGGAAAACGTATTATCAATTCAGCAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20456651..20456700 26863196 MeRIP-seq:(Medium) rs747207116 Functional Loss SNV dbSNP153 33..33 33 - - - 104828 RMVar_ID_104828 Human_SNP_ID_547172509 m1A Human chr14 - 20456663 20456663 20456663 GTATATCTGGGGCTTCTTCCTTTACCCACTGTAAGTGAAAAGAAAGGTGGAAAACGTATTATCAA GTATATCTGGGGCTTCTTCCTTTACCCACTGTTAGTGAAAAGAAAGGTGGAAAACGTATTATCAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:20456661..20456855 26863196 MeRIP-seq:(Medium) rs776532738 Functional Loss SNV dbSNP153 33..33 33 - - - 104829 RMVar_ID_104829 Human_SNP_ID_547172780 m1A Human chr14 + 20457202 20457202 20457202 CTGTGTGGAGACCTCAATGTGGCACATGAAGAAATTGACCTTCGCAACCCCAAGGGGAACAAAAA CTGTGTGGAGACCTCAATGTGGCACATGAAGAGATTGACCTTCGCAACCCCAAGGGGAACAAAAA A G APEX1 Ensembl:ENSG00000100823 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20457151..20457500 32194978 MeRIP-seq:(Medium) rs771931978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442707,Human_RBP_ID_1490417,Human_RBP_ID_1815985,Human_RBP_ID_9340827,Human_RBP_ID_17845863,Human_RBP_ID_18647197,Human_RBP_ID_22045128,Human_RBP_ID_23615061,Human_RBP_ID_26921914,Human_RBP_ID_27225138 Human_Splice_Rec_1488422 104830 RMVar_ID_104830 Human_SNP_ID_547173289 m1A Human chr14 + 20458661 20458661 20458661 ACAGCCAACAGGATGACAAATGCCCAGGCTGCATAGATGCCTCCATATCGCCGTGCATGCTTCCA ACAGCCAACAGGATGACAAATGCCCAGGCTGCGTAGATGCCTCCATATCGCCGTGCATGCTTCCA A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:20458551..20458737 26863196 MeRIP-seq:(Medium) rs201678318 Functional Loss SNV dbSNP153 33..33 33 - - - 104831 RMVar_ID_104831 Human_SNP_ID_547173290 m1A Human chr14 - 20458662 20458662 20458662 ATGGAAGCATGCACGGCGATATGGAGGCATCTATGCAGCCTGGGCATTTGTCATCCTGTTGGCTG ATGGAAGCATGCACGGCGATATGGAGGCATCTGTGCAGCCTGGGCATTTGTCATCCTGTTGGCTG T C PIP4P1 Ensembl:ENSG00000165782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20458448..20458725 26863196 MeRIP-seq:(Medium) rs1249307306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442750,Human_RBP_ID_1490446,Human_RBP_ID_5493313,Human_RBP_ID_18647212,Human_RBP_ID_25122901 Human_Splice_Rec_1488458,Human_Splice_Rec_1488464,Human_Splice_Rec_1488465,Human_Splice_Rec_1488480,Human_Splice_Rec_1488488,Human_Splice_Rec_1488492 104832 RMVar_ID_104832 Human_SNP_ID_547173887 m1A Human chr14 - 20460713 20460713 20460713 GATCACCTGCCGAGTCTGCCAATCTCTCATCAACGTGGAAGGCAAGATGCATCAGCATGTAGTCA GATCACCTGCCGAGTCTGCCAATCTCTCATCATCGTGGAAGGCAAGATGCATCAGCATGTAGTCA T A PIP4P1 Ensembl:ENSG00000165782 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20460623..20460723 32194978 MeRIP-seq:(Medium) rs779170117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442754,Human_RBP_ID_880455,Human_RBP_ID_1816001,Human_RBP_ID_4286275,Human_RBP_ID_8250058,Human_RBP_ID_18647221 Human_Splice_Rec_1488449,Human_Splice_Rec_1488471,Human_Splice_Rec_1488493 104833 RMVar_ID_104833 Human_SNP_ID_547173923 m1A Human chr14 - 20460797 20460797 20460797 CGAGGGGCATCCAGCCGTGTTGCCTGGGGAGGACCCACCCCCCTATTCACCCTTAACTAGCCCGG CGAGGGGCATCCAGCCGTGTTGCCTGGGGAGGGCCCACCCCCCTATTCACCCTTAACTAGCCCGG T C PIP4P1 Ensembl:ENSG00000165782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20460746..20460850 26863196 MeRIP-seq:(Medium) rs879247041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430212 Human_Splice_Rec_1488448,Human_Splice_Rec_1488470 104834 RMVar_ID_104834 Human_SNP_ID_547174158 m1A Human chr14 + 20461390 20461390 20461390 GATCCGGCTCCCTTCGCCTCTGCCGTCGCCGCAGCCACCGCCACCGCCGCCACCGCCACCGCCGC GATCCGGCTCCCTTCGCCTCTGCCGTCGCCGCCGCCACCGCCACCGCCGCCACCGCCACCGCCGC A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:20461130..20461472;chr14:20461119..20461530;chr14:20461133..20461500;chr14:20461146..20461513 26863196 MeRIP-seq:(Medium) rs1387232751 Functional Loss SNV dbSNP153 33..33 33 - - - 104835 RMVar_ID_104835 Human_SNP_ID_547176230 m1A Human chr14 + 20469686 20469686 20469686 AGAGGCCTGGCACTGAGCCTAGTGTCGGGAGCAAGGCGGCAGAGTCATGCGGCAGCCAGCGCGGG AGAGGCCTGGCACTGAGCCTAGTGTCGGGAGCCAGGCGGCAGAGTCATGCGGCAGCCAGCGCGGG A C PNP Ensembl:ENSG00000198805 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:20469683..20469772 26863196 MeRIP-seq:(Medium) rs960757933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1488525 104836 RMVar_ID_104836 Human_SNP_ID_547176915 m1A Human chr14 + 20472322 20472322 20472322 ATATTTTTTCTCCCCCAGATACACCTATGAAGATTATAAGAACACTGCAGAATGGCTTCTGTCTC ATATTTTTTCTCCCCCAGATACACCTATGAAGGTTATAAGAACACTGCAGAATGGCTTCTGTCTC A G PNP Ensembl:ENSG00000198805 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:20472301..20472375 26863196 MeRIP-seq:(Medium) rs1198353300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231399,Human_RBP_ID_1171366,Human_RBP_ID_1490463,Human_RBP_ID_1816004,Human_RBP_ID_3443642,Human_RBP_ID_4310889,Human_RBP_ID_5493315,Human_RBP_ID_9368267,Human_RBP_ID_12291035,Human_RBP_ID_17845883,Human_RBP_ID_18979104,Human_RBP_ID_22184452,Human_RBP_ID_22438439,Human_RBP_ID_26325585 Human_Splice_Rec_1488498,Human_Splice_Rec_1488502,Human_Splice_Rec_1488504,Human_Splice_Rec_1488508,Human_Splice_Rec_1488518,Human_Splice_Rec_1488526,Human_Splice_Rec_1488534 RMVar_hsa_circ_108126,RMVar_hsa_circ_165115 104837 RMVar_ID_104837 Human_SNP_ID_547177518 m1A Human chr14 + 20474573 20474573 20474573 GGTTCCACATGTATGAAGGGTACCCACTCTGGAAGGTAAGTCAGAGGGATAGGTCCGGTTGGATC GGTTCCACATGTATGAAGGGTACCCACTCTGGGAGGTAAGTCAGAGGGATAGGTCCGGTTGGATC A G PNP Ensembl:ENSG00000198805 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20474476..20474600 32194978 MeRIP-seq:(Medium) rs1473859214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3443647,Human_RBP_ID_9323715,Human_RBP_ID_19063554,Human_RBP_ID_22414958,Human_RBP_ID_22439513,Human_RBP_ID_26324804 Human_Splice_Rec_1488511,Human_Splice_Rec_1488529,Human_Splice_Rec_1488537 Human_miRNA_ID_2825390,Human_miRNA_ID_2859361 RMVar_hsa_circ_108126,RMVar_hsa_circ_165115 104838 RMVar_ID_104838 Human_SNP_ID_547177588 m1A Human chr14 - 20474753 20474753 20474753 CTGGGAATGTCACCTTCGAAGCAAACAATCCGAAAAAAATTTACAAAATTTCATTAATTCAGCTA CTGGGAATGTCACCTTCGAAGCAAACAATCCGGAAAAAATTTACAAAATTTCATTAATTCAGCTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20474751..20474966 32194978 MeRIP-seq:(Medium) rs763807017 Functional Loss SNV dbSNP153 33..33 33 - - - 104839 RMVar_ID_104839 Human_SNP_ID_547178117 m1A Human chr14 + 20476546 20476546 20476546 AGCAGCTGGCAAACAAGCTGCACAGAAATTGGAACAGTTTGTCTCCATTCTTATGGCCAGCATTC AGCAGCTGGCAAACAAGCTGCACAGAAATTGGGACAGTTTGTCTCCATTCTTATGGCCAGCATTC A G PNP Ensembl:ENSG00000198805 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20476495..20476951 32194978 MeRIP-seq:(Medium) rs773751064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1171368,Human_RBP_ID_1274198,Human_RBP_ID_1490491,Human_RBP_ID_8401164,Human_RBP_ID_22757810,Human_RBP_ID_27225172 Clinvar_Rec_670 104840 RMVar_ID_104840 Human_SNP_ID_547213054 m1A Human chr14 - 20609351 20609351 20609351 TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCTGTTCCTTTTTTCTTTC TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCACATCCCGGACGAGCCCTGTTCCTTTTTTCTTTC T G AL163195.3,RNASE11 Ensembl:ENSG00000259060,Ensembl:ENSG00000173464 Protein coding,Protein coding intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1159012438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38511,Human_RBP_ID_119438,Human_RBP_ID_1502709,Human_RBP_ID_5274277,Human_RBP_ID_5463205,Human_RBP_ID_5493318,Human_RBP_ID_6330466,Human_RBP_ID_8250060,Human_RBP_ID_8401178,Human_RBP_ID_12291155,Human_RBP_ID_17845905,Human_RBP_ID_18545337,Human_RBP_ID_19920213,Human_RBP_ID_22798572,Human_RBP_ID_23126673,Human_RBP_ID_23615116,Human_RBP_ID_24551658,Human_RBP_ID_27430225,Human_RBP_ID_27837301 104841 RMVar_ID_104841 Human_SNP_ID_547213524 m1A Human chr14 + 20610198 20610198 20610198 AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGAATCCCACCGCTGCCAGGTGCTTCCCTTTTCTT AAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGGATCCCACCGCTGCCAGGTGCTTCCCTTTTCTT A G tRNA-Leu-AAG-2-3 RNACentral:URS0000120E41 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs757521490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442785,Human_RBP_ID_1171372,Human_RBP_ID_1502711,Human_RBP_ID_3443658,Human_RBP_ID_5274280,Human_RBP_ID_5418011,Human_RBP_ID_5463206,Human_RBP_ID_6406390,Human_RBP_ID_8250063,Human_RBP_ID_8401183,Human_RBP_ID_9039877,Human_RBP_ID_9758937,Human_RBP_ID_18647251,Human_RBP_ID_19920218,Human_RBP_ID_22797310,Human_RBP_ID_23126679,Human_RBP_ID_23615121,Human_RBP_ID_24472810,Human_RBP_ID_26921950 104842 RMVar_ID_104842 Human_SNP_ID_547213566 m1A Human chr14 - 20610227 20610227 20610227 ACTAATCGGAATACACGGATGGTTTCCCCAAGAAAAGGGAAGCACCTGGCAGCGGTGGGATTCGA ACTAATCGGAATACACGGATGGTTTCCCCAAGGAAAGGGAAGCACCTGGCAGCGGTGGGATTCGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:20610178..20610304 26863196 MeRIP-seq:(Medium) rs998112832 Functional Loss SNV dbSNP153 33..33 33 - - - 104843 RMVar_ID_104843 Human_SNP_ID_547213574 m1A Human chr14 + 20610235 20610235 20610235 CACCGCTGCCAGGTGCTTCCCTTTTCTTGGGGAAACCATCCGTGTATTCCGATTAGTGTACTGGT CACCGCTGCCAGGTGCTTCCCTTTTCTTGGGGTAACCATCCGTGTATTCCGATTAGTGTACTGGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20610217..20610301 26863196 MeRIP-seq:(Medium) rs533286464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274281,Human_RBP_ID_23126679 104844 RMVar_ID_104844 Human_SNP_ID_547214398 m1A Human chr14 - 20613356 20613356 20613356 ACTCAACAAGGTGTGTCTTGTTTGAAAACTTCACGACTGCACTTTGCTGTCCCTGTATACCGTTC ACTCAACAAGGTGTGTCTTGTTTGAAAACTTCCCGACTGCACTTTGCTGTCCCTGTATACCGTTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:20613276..20613428 26863196 MeRIP-seq:(Medium) rs915400736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1274201,Human_RBP_ID_1816023,Human_RBP_ID_3443661,Human_RBP_ID_23126684 104845 RMVar_ID_104845 Human_SNP_ID_547214400 m1A Human chr14 + 20613359 20613359 20613359 CGGTATACAGGGACAGCAAAGTGCAGTCGTGAAGTTTTCAAACAAGACACACCTTGTTGAGTTGA CGGTATACAGGGACAGCAAAGTGCAGTCGTGACGTTTTCAAACAAGACACACCTTGTTGAGTTGA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr14:20613251..20613425;chr14:20613251..20613440 26863196 MeRIP-seq:(Medium) rs535716298 Functional Loss SNV dbSNP153 33..33 33 - - - 104846 RMVar_ID_104846 Human_SNP_ID_547214402 m1A Human chr14 - 20613363 20613363 20613363 CTTTTCAACTCAACAAGGTGTGTCTTGTTTGAAAACTTCACGACTGCACTTTGCTGTCCCTGTAT CTTTTCAACTCAACAAGGTGTGTCTTGTTTGAGAACTTCACGACTGCACTTTGCTGTCCCTGTAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:20613314..20613403 26863196 MeRIP-seq:(Medium) rs571900382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1274201,Human_RBP_ID_1490514,Human_RBP_ID_1816023,Human_RBP_ID_3443661,Human_RBP_ID_19920229,Human_RBP_ID_22184471,Human_RBP_ID_23126685 104847 RMVar_ID_104847 Human_SNP_ID_547214435 m1A Human chr14 + 20613396 20613396 20613396 TCAAACAAGACACACCTTGTTGAGTTGAAAAGAGCGAGGGCTCGTCCGGGATTTGAACCCGGGAC TCAAACAAGACACACCTTGTTGAGTTGAAAAGCGCGAGGGCTCGTCCGGGATTTGAACCCGGGAC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:20613291..20613413 26863196 MeRIP-seq:(Medium) rs530354846 Functional Loss SNV dbSNP153 33..33 33 - - - 104848 RMVar_ID_104848 Human_SNP_ID_547214436 m1A Human chr14 + 20613396 20613396 20613396 TCAAACAAGACACACCTTGTTGAGTTGAAAAGAGCGAGGGCTCGTCCGGGATTTGAACCCGGGAC TCAAACAAGACACACCTTGTTGAGTTGAAAAGGGCGAGGGCTCGTCCGGGATTTGAACCCGGGAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:20613291..20613413 26863196 MeRIP-seq:(Medium) rs530354846 Functional Loss SNV dbSNP153 33..33 33 - - - 104849 RMVar_ID_104849 Human_SNP_ID_547214484 m1A Human chr14 - 20613416 20613416 20613416 TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCTCGCTCTTTTCAACTCA TCTCGCTTAGGGTGCGAGAGGTCCCGGGTTCACATCCCGGACGAGCCCTCGCTCTTTTCAACTCA T G TRP2,TRP-AGG1-1 RNACentral:URS00005DB87D,RNACentral:URS0000416117 tRNA,tRNA intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1288773824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1490515,Human_RBP_ID_8250065,Human_RBP_ID_8401186,Human_RBP_ID_9039880,Human_RBP_ID_12291166,Human_RBP_ID_18647253,Human_RBP_ID_19030693,Human_RBP_ID_20001683,Human_RBP_ID_22798576,Human_RBP_ID_23126686 104850 RMVar_ID_104850 Human_SNP_ID_547214855 m1A Human chr14 - 20613805 20613805 20613805 GCTGGTCTTGTAAACCAGGGGTCGCGAGTTCAATTCTCGCTGGGGCCTGTGTGTTTTTTCCTCCT GCTGGTCTTGTAAACCAGGGGTCGCGAGTTCAGTTCTCGCTGGGGCCTGTGTGTTTTTTCCTCCT T C TRT-TGT3-1,tRNA-Thr-TGT-3-1 RNACentral:URS00003516B6,RNACentral:URS0000725A6A tRNA,tRNA intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs528147567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269589,Human_RBP_ID_442787,Human_RBP_ID_1171375,Human_RBP_ID_1236888,Human_RBP_ID_1274203,Human_RBP_ID_1361001,Human_RBP_ID_1490519,Human_RBP_ID_3443663,Human_RBP_ID_5175886,Human_RBP_ID_5257836,Human_RBP_ID_5274374,Human_RBP_ID_5493321,Human_RBP_ID_6330474,Human_RBP_ID_8401190,Human_RBP_ID_8793471,Human_RBP_ID_17845909,Human_RBP_ID_18177475,Human_RBP_ID_18199577,Human_RBP_ID_18435659,Human_RBP_ID_18647254,Human_RBP_ID_19920234,Human_RBP_ID_21923972,Human_RBP_ID_22798578,Human_RBP_ID_23126697,Human_RBP_ID_23615124,Human_RBP_ID_24410190,Human_RBP_ID_24470930 104851 RMVar_ID_104851 Human_SNP_ID_547218114 m1A Human chr14 + 20625436 20625436 20625436 TAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGAATCCCACCACTGCCAGTGGTACGTTTTAGCAC TAGGCTCCAGTCTCTTCGGGGGCGTGGGTTCGGATCCCACCACTGCCAGTGGTACGTTTTAGCAC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs754033417 Functional Loss SNV dbSNP153 33..33 33 - - - 104852 RMVar_ID_104852 Human_SNP_ID_547219908 m1A Human chr14 - 20631175 20631175 20631175 ACTGGTCTTGTAAACCAGGGGTCGCGAGTTCAAATCTCGCTGGGGCCTCGGCTGTAGGAATACTT ACTGGTCTTGTAAACCAGGGGTCGCGAGTTCACATCTCGCTGGGGCCTCGGCTGTAGGAATACTT T G tRNA-Thr-TGT-6-1,TRT-TGT3-1,piR-44992,tRNA-Thr-TGT-4-1 RNACentral:URS000068C296,RNACentral:URS00003516B6,RNACentral:URS0000303F94,RNACentral:URS000021550A tRNA,tRNA,piRNA,tRNA intron,intron,intron,intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA untreated chr14:20631137..20631213 29072297,31548705,26863196 m1A-MAP&m1A-IP-seq:(High) rs1363389643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442796,Human_RBP_ID_1361004,Human_RBP_ID_1490534,Human_RBP_ID_3443670,Human_RBP_ID_8250069,Human_RBP_ID_8401204,Human_RBP_ID_9758941,Human_RBP_ID_16996290,Human_RBP_ID_19920254,Human_RBP_ID_22798583,Human_RBP_ID_22926548,Human_RBP_ID_23126716,Human_RBP_ID_23615134,Human_RBP_ID_26929492 104853 RMVar_ID_104853 Human_SNP_ID_547220638 m1A Human chr14 + 20633062 20633049 20633062 TCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCCTTTACTTTCCTTTCCG TCTCGCTTTGGGTGCGAGAG_____________ATCCCGGACGAGCCCCTTTACTTTCCTTTCCG GGTCCCGGGTTCAA G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs933470456 Functional Loss DEL dbSNP153 21..33 33 - - - 104854 RMVar_ID_104854 Human_SNP_ID_547220638 m1A Human chr14 + 20633061 20633049 20633062 TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCCTTTACTTTCCTTTCC TTCTCGCTTTGGGTGCGAGAG_____________ATCCCGGACGAGCCCCTTTACTTTCCTTTCC GGTCCCGGGTTCAA G lnc-RNASE4-1,tRNA-Pro-TGG-1-1 RNACentral:URS0000D571B6,RNACentral:URS0000493225 lincRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs933470456 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_5274286,Human_RBP_ID_8401211,Human_RBP_ID_17364568,Human_RBP_ID_17845915,Human_RBP_ID_19920258,Human_RBP_ID_22798584,Human_RBP_ID_23126727,Human_RBP_ID_24470935 104855 RMVar_ID_104855 Human_SNP_ID_547220662 m1A Human chr14 + 20633061 20633061 20633061 TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCCTTTACTTTCCTTTCC TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCGAATCCCGGACGAGCCCCTTTACTTTCCTTTCC A G lnc-RNASE4-1,tRNA-Pro-TGG-1-1 RNACentral:URS0000D571B6,RNACentral:URS0000493225 lincRNA,tRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1421445114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274286,Human_RBP_ID_8401211,Human_RBP_ID_17364568,Human_RBP_ID_17845915,Human_RBP_ID_19920258,Human_RBP_ID_22798584,Human_RBP_ID_23126727,Human_RBP_ID_24470935 104856 RMVar_ID_104856 Human_SNP_ID_547220732 m1A Human chr14 + 20633113 20633113 20633113 TACTTTCCTTTCCGTTTCATCTTTCTCTCTTTAAAGTCAGTAGTTAACAAATACTGCAATCGGCG TACTTTCCTTTCCGTTTCATCTTTCTCTCTTTGAAGTCAGTAGTTAACAAATACTGCAATCGGCG A G lnc-RNASE4-1 RNACentral:URS0000D571B6 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20633033..20633259 26863196 MeRIP-seq:(Medium) rs1340724839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3443672,Human_RBP_ID_6330492,Human_RBP_ID_19909189,Human_RBP_ID_22184483,Human_RBP_ID_24470936,Human_RBP_ID_26921968,Human_RBP_ID_27225197 104857 RMVar_ID_104857 Human_SNP_ID_547220737 m1A Human chr14 + 20633119 20633119 20633119 CCTTTCCGTTTCATCTTTCTCTCTTTAAAGTCAGTAGTTAACAAATACTGCAATCGGCGCTACGG CCTTTCCGTTTCATCTTTCTCTCTTTAAAGTCGGTAGTTAACAAATACTGCAATCGGCGCTACGG A G lnc-RNASE4-1 RNACentral:URS0000D571B6 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr14:20633051..20633250;chr14:20633072..20633237 26863196 MeRIP-seq:(Medium) rs151071790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3443672,Human_RBP_ID_19909189,Human_RBP_ID_22184483,Human_RBP_ID_24470936,Human_RBP_ID_26921968,Human_RBP_ID_27225197 104858 RMVar_ID_104858 Human_SNP_ID_547220743 m1A Human chr14 + 20633127 20633125 20633128 TTTCATCTTTCTCTCTTTAAAGTCAGTAGTTAACAAATACTGCAATCGGCGCTACGGCTAGGTCA TTTCATCTTTCTCTCTTTAAAGTCAGTAGTT___AAATACTGCAATCGGCGCTACGGCTAGGTCA TAAC T lnc-RNASE4-1 RNACentral:URS0000D571B6 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:20633077..20633204 26863196 MeRIP-seq:(Medium) rs527310454 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_19920258,Human_RBP_ID_23126733,Human_RBP_ID_26921968 104859 RMVar_ID_104859 Human_SNP_ID_547220746 m1A Human chr14 + 20633127 20633127 20633127 TTTCATCTTTCTCTCTTTAAAGTCAGTAGTTAACAAATACTGCAATCGGCGCTACGGCTAGGTCA TTTCATCTTTCTCTCTTTAAAGTCAGTAGTTAGCAAATACTGCAATCGGCGCTACGGCTAGGTCA A G lnc-RNASE4-1 RNACentral:URS0000D571B6 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:20633077..20633204 26863196 MeRIP-seq:(Medium) rs947374235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19920258,Human_RBP_ID_23126733,Human_RBP_ID_26921968 104860 RMVar_ID_104860 Human_SNP_ID_547227632 m1A Human chr14 - 20657479 20657479 20657479 ACATTTGCGGACATCCTTAGGTCGCTGGTTCGATTCCAGCTCGAAGGAAGTGCGTGATGCTTTTG ACATTTGCGGACATCCTTAGGTCGCTGGTTCGGTTCCAGCTCGAAGGAAGTGCGTGATGCTTTTG T C tRNA-Tyr,lnc-OR6S1-2,TRY-GTA1-1,TRY-GTA4-1,tRNA-Tyr-GTA-4-1 RNACentral:URS00001E28FC,RNACentral:URS00008C1F55,RNACentral:URS00002CA973,RNACentral:URS00007282DA,RNACentral:URS000073FCEB tRNA,lincRNA,tRNA,tRNA,tRNA exon,intron,exon,exon,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1228520526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442803,Human_RBP_ID_1171386,Human_RBP_ID_1490540,Human_RBP_ID_1816037,Human_RBP_ID_3443675,Human_RBP_ID_4310936,Human_RBP_ID_5178413,Human_RBP_ID_5246987,Human_RBP_ID_5257842,Human_RBP_ID_5536089,Human_RBP_ID_6330504,Human_RBP_ID_8250074,Human_RBP_ID_8401214,Human_RBP_ID_9039888,Human_RBP_ID_12291206,Human_RBP_ID_17364575,Human_RBP_ID_17686975,Human_RBP_ID_17845924,Human_RBP_ID_18647278,Human_RBP_ID_19920272,Human_RBP_ID_22797326,Human_RBP_ID_23126746,Human_RBP_ID_23615146,Human_RBP_ID_26427767,Human_RBP_ID_26623172,Human_RBP_ID_26748514,Human_RBP_ID_26921975,Human_RBP_ID_27225202 104861 RMVar_ID_104861 Human_SNP_ID_547229681 m1A Human chr14 - 20664291 20664291 20664291 AGGCGGCAGAATCGCTTGAACCTGGGAGGCGGAGGTGGCGGTGAGCTGAGATCGCGCCATTTCAC AGGCGGCAGAATCGCTTGAACCTGGGAGGCGGTGGTGGCGGTGAGCTGAGATCGCGCCATTTCAC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr14:20664207..20664291 26863410 MeRIP-seq:(Medium) rs1012243844 Functional Loss SNV dbSNP153 33..33 33 - - - 104862 RMVar_ID_104862 Human_SNP_ID_547234230 m1A Human chr14 + 20681746 20681746 20681746 CACTGGTCTTGTAAACCAGGGGTCGCGAGTTCAAATCTCGCTGGGGCCTTGCGAAACTACTTTCT CACTGGTCTTGTAAACCAGGGGTCGCGAGTTCGAATCTCGCTGGGGCCTTGCGAAACTACTTTCT A G tRNA-Thr-TGT-5-1,piR-44992 RNACentral:URS00000F30A4,RNACentral:URS0000303F94 tRNA,piRNA exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1402640355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442818,Human_RBP_ID_1490549,Human_RBP_ID_8250089,Human_RBP_ID_8401227,Human_RBP_ID_9039892,Human_RBP_ID_9758951,Human_RBP_ID_17845928,Human_RBP_ID_18647293,Human_RBP_ID_19920292,Human_RBP_ID_22042751,Human_RBP_ID_22797336,Human_RBP_ID_22921897,Human_RBP_ID_23126771,Human_RBP_ID_23615162,Human_RBP_ID_24410195,Human_RBP_ID_24470943,Human_RBP_ID_25124425,Human_RBP_ID_26921979 104863 RMVar_ID_104863 Human_SNP_ID_547235180 m1A Human chr14 + 20684071 20684059 20684072 TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCTCGTGGCTACTGTTTT TTCTCGCTTTGGGTGCGAGAG_____________ATCCCGGACGAGCCCTCGTGGCTACTGTTTT GGTCCCGGGTTCAA G tRNA-Pro-TGG-3-2 RNACentral:URS00002D40C8 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1160885299 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_1171394,Human_RBP_ID_1490553,Human_RBP_ID_5175896,Human_RBP_ID_8250093,Human_RBP_ID_8401234,Human_RBP_ID_12291234,Human_RBP_ID_18207023,Human_RBP_ID_18647301,Human_RBP_ID_19920313,Human_RBP_ID_22042753,Human_RBP_ID_22797345,Human_RBP_ID_22926768,Human_RBP_ID_23126788,Human_RBP_ID_23615168,Human_RBP_ID_24410197,Human_RBP_ID_24470946,Human_RBP_ID_26921981,Human_RBP_ID_27225208 104864 RMVar_ID_104864 Human_SNP_ID_547235208 m1A Human chr14 + 20684071 20684071 20684071 TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCTCGTGGCTACTGTTTT TTCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCGAATCCCGGACGAGCCCTCGTGGCTACTGTTTT A G tRNA-Pro-TGG-3-2 RNACentral:URS00002D40C8 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1490501322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1171394,Human_RBP_ID_1490553,Human_RBP_ID_5175896,Human_RBP_ID_8250093,Human_RBP_ID_8401234,Human_RBP_ID_12291234,Human_RBP_ID_18207023,Human_RBP_ID_18647301,Human_RBP_ID_19920313,Human_RBP_ID_22042753,Human_RBP_ID_22797345,Human_RBP_ID_22926768,Human_RBP_ID_23126788,Human_RBP_ID_23615168,Human_RBP_ID_24410197,Human_RBP_ID_24470946,Human_RBP_ID_26921981,Human_RBP_ID_27225208 104865 RMVar_ID_104865 Human_SNP_ID_547237771 m1A Human chr14 - 20693611 20693611 20693611 TATCCTGAGCCAGGGTCGGTGGGGTCAGACCCAGACCCAGCACGAAGACCAACAACAAAACGCCC TATCCTGAGCCAGGGTCGGTGGGGTCAGACCCGGACCCAGCACGAAGACCAACAACAAAACGCCC T C EGILA Ensembl:ENSG00000258451 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20693527..20693721 32194978 MeRIP-seq:(Medium) rs201878808 Functional Loss SNV dbSNP153 33..33 33 - - - 104866 RMVar_ID_104866 Human_SNP_ID_547237772 m1A Human chr14 - 20693611 20693611 20693611 TATCCTGAGCCAGGGTCGGTGGGGTCAGACCCAGACCCAGCACGAAGACCAACAACAAAACGCCC TATCCTGAGCCAGGGTCGGTGGGGTCAGACCCCGACCCAGCACGAAGACCAACAACAAAACGCCC T G EGILA Ensembl:ENSG00000258451 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20693527..20693721 32194978 MeRIP-seq:(Medium) rs201878808 Functional Loss SNV dbSNP153 33..33 33 - - - 104867 RMVar_ID_104867 Human_SNP_ID_547315253 m1A Human chr14 - 20992093 20992093 20992093 GTCTGTGGTGAGAACAAGGACTGGAAGTCAGGACCTAGGGAGAACAGGGCTCAGATCCAATATCT GTCTGTGGTGAGAACAAGGACTGGAAGTCAGGCCCTAGGGAGAACAGGGCTCAGATCCAATATCT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20992088..20992189 32194978 MeRIP-seq:(Medium) rs1566431509 Functional Loss SNV dbSNP153 33..33 33 - - - 104868 RMVar_ID_104868 Human_SNP_ID_547315420 m1A Human chr14 - 20992619 20992619 20992619 GTTCAGGTTGGAAGTTAAGGGACTTTCACCTCATGGAATGCTCTGGAGACTGCTGCAAAGCCACC GTTCAGGTTGGAAGTTAAGGGACTTTCACCTCGTGGAATGCTCTGGAGACTGCTGCAAAGCCACC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:20992574..20992678 26863410 MeRIP-seq:(Medium) rs1169987668 Functional Loss SNV dbSNP153 33..33 33 - - - 104869 RMVar_ID_104869 Human_SNP_ID_547315527 m1A Human chr14 - 20993079 20993079 20993079 AAATATACAACATCCCACAGTAGGGTAATTAGATACTTATTTAGGACCTTGATAAATGTGAATTA AAATATACAACATCCCACAGTAGGGTAATTAGCTACTTATTTAGGACCTTGATAAATGTGAATTA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:20993077..20993246 26863410 MeRIP-seq:(Medium) rs767815498 Functional Loss SNV dbSNP153 33..33 33 - - - 104870 RMVar_ID_104870 Human_SNP_ID_547315530 m1A Human chr14 - 20993090 20993090 20993090 CGGATCTGAAGAAATATACAACATCCCACAGTAGGGTAATTAGATACTTATTTAGGACCTTGATA CGGATCTGAAGAAATATACAACATCCCACAGTGGGGTAATTAGATACTTATTTAGGACCTTGATA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:20993084..20993188 26863410 MeRIP-seq:(Medium) rs78713618 Functional Loss SNV dbSNP153 33..33 33 - - - 104871 RMVar_ID_104871 Human_SNP_ID_547315561 m1A Human chr14 - 20993177 20993177 20993177 CTGAAGAAAGTTACTCACCAGGTGACAGAACCAGTACCTGAGCCAAAGTCCATCAAAGTTTGTGG CTGAAGAAAGTTACTCACCAGGTGACAGAACCGGTACCTGAGCCAAAGTCCATCAAAGTTTGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20993126..20993200 26863196 MeRIP-seq:(Medium) rs761007284 Functional Loss SNV dbSNP153 33..33 33 - - - 104872 RMVar_ID_104872 Human_SNP_ID_547315900 m1A Human chr14 - 20993981 20993981 20993981 CACATATATTCACGTAGGCTCTGGCCCCAAATACTGTGAGCAGCCCTAAGATGGCAAAATTATTA CACATATATTCACGTAGGCTCTGGCCCCAAATCCTGTGAGCAGCCCTAAGATGGCAAAATTATTA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:20993951..20994075 26863196 MeRIP-seq:(Medium) rs781343851 Functional Loss SNV dbSNP153 33..33 33 - - - 104873 RMVar_ID_104873 Human_SNP_ID_547322018 m1A Human chr14 - 21016987 21016982 21016987 TGTGGGGAAGGATTGGTGCTGGGGCAACAGGAAGGGGCCTGGGGCCGTTTGGCTGCACTAACTTT TGTGGGGAAGGATTGGTGCTGGGGCAACAGGA_____CCTGGGGCCGTTTGGCTGCACTAACTTT GCCCCT G NDRG2 Ensembl:ENSG00000165795 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:21016938..21017067 26863196 MeRIP-seq:(Medium) rs1447482305 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_758415,Human_RBP_ID_5112517,Human_RBP_ID_5140717,Human_RBP_ID_8181402,Human_RBP_ID_9352902,Human_RBP_ID_17651286,Human_RBP_ID_17845950,Human_RBP_ID_18161194,Human_RBP_ID_21968909,Human_RBP_ID_22540204,Human_RBP_ID_23208468,Human_RBP_ID_26431554 104874 RMVar_ID_104874 Human_SNP_ID_547322129 m1A Human chr14 + 21017468 21017467 21017468 AAAGGTCAAGGTTAGGGTAGCAATCAAAGATCAAGGTCATCTCCCCGCATGATCTGCCCTTTTTC AAAGGTCAAGGTTAGGGTAGCAATCAAAGATC_AGGTCATCTCCCCGCATGATCTGCCCTTTTTC CA C NONHSAG014396.2,NONHSAG014396.2:2 RNACentral:URS00008C35E0,RNACentral:URS00008C3B51 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21017365..21017483 26863196 MeRIP-seq:(Medium) rs955995222 Functional Loss DEL dbSNP153 33..33 33 - - - 104875 RMVar_ID_104875 Human_SNP_ID_547324457 m1A Human chr14 + 21024963 21024963 21024963 GAGCCTCCAGCTCCAGGGGACGCGGATCAATCACACCGCCCGCCGGCCCGGCTGGCGCCTTCCAG GAGCCTCCAGCTCCAGGGGACGCGGATCAATCCCACCGCCCGCCGGCCCGGCTGGCGCCTTCCAG A C AL161668.4,TPPP2 Ensembl:ENSG00000258604,Ensembl:ENSG00000179636 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21024962..21025046 26863196 MeRIP-seq:(Medium) rs1237462596 Functional Loss SNV dbSNP153 33..33 33 - - - 104876 RMVar_ID_104876 Human_SNP_ID_547337228 m1A Human chr14 + 21074607 21074607 21074607 GCCACCGGAGACACCGGGCGTGGATGCACCAGAAGGGCCTGGGGCCTCGGGGCCAGGATGGAGCA GCCACCGGAGACACCGGGCGTGGATGCACCAGGAGGGCCTGGGGCCTCGGGGCCAGGATGGAGCA A G ARHGEF40 Ensembl:ENSG00000165801 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12889267 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5352613,Human_RBP_ID_5522570,Human_RBP_ID_22926382 GWAS_ID_13701,GWAS_ID_13702,GWAS_ID_13703,GWAS_ID_13704,GWAS_ID_13705,GWAS_ID_13706,GWAS_ID_13707,GWAS_ID_13708,GWAS_ID_13709,GWAS_ID_13710,GWAS_ID_13711,GWAS_ID_13712,GWAS_ID_13713,GWAS_ID_13714,GWAS_ID_13715,GWAS_ID_13716 RMVar_hsa_circ_78048,RMVar_hsa_circ_66452,RMVar_hsa_circ_109003,RMVar_hsa_circ_266567,RMVar_hsa_circ_165125,RMVar_hsa_circ_165126 104877 RMVar_ID_104877 Human_SNP_ID_547337363 m1A Human chr14 - 21074921 21074921 21074921 GCATCTTCCTTGTCCCCAGGGCTCAGTGGGGCACTGTCCCCTCCTCGGCTAAGAGCCCCTCGACC GCATCTTCCTTGTCCCCAGGGCTCAGTGGGGCCCTGTCCCCTCCTCGGCTAAGAGCCCCTCGACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21074771..21074967 26863196 MeRIP-seq:(Medium) rs1464262494 Functional Loss SNV dbSNP153 33..33 33 - - - 104878 RMVar_ID_104878 Human_SNP_ID_547342086 m1A Human chr14 + 21090782 21090782 21090782 GGGCAGAAGAGGCAGCGGTGGAGGGCACCCCCAGGCCCGGCCTCGCCTCCCGGCCCTGCCCGCAA GGGCAGAAGAGGCAGCGGTGGAGGGCACCCCCGGGCCCGGCCTCGCCTCCCGGCCCTGCCCGCAA A G NONHSAG014406.2,NONHSAG014406.2:2 RNACentral:URS00008C2546,RNACentral:URS000012EACC lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:21090494..21090893 32194978 MeRIP-seq:(Medium) rs764630401 Functional Loss SNV dbSNP153 33..33 33 - - - 104879 RMVar_ID_104879 Human_SNP_ID_547342664 m1A Human chr14 + 21092086 21092072 21092087 GGAGAGCAGAGGACAGCGGGCGGAAGCCTCCGAAGCTGCGGCCGGGACCGGGCTCAGCACCCTCG GGAGAGCAGAGGACAGCGG_______________GCTGCGGCCGGGACCGGGCTCAGCACCCTCG GGCGGAAGCCTCCGAA G NONHSAG014406.2,NONHSAG014406.2:2 RNACentral:URS00008C2546,RNACentral:URS000012EACC lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21092035..21092110 26863196 MeRIP-seq:(Medium) rs751641354 Functional Loss DEL dbSNP153 20..34 33 - - - 104880 RMVar_ID_104880 Human_SNP_ID_547342900 m1A Human chr14 + 21092601 21092600 21092601 ACTGATCTGGGTTCGGGCTGGGGTGGAGGCTGAGGCTGAGGCTGAGGCGGAGGCGCAGCGGAGGT ACTGATCTGGGTTCGGGCTGGGGTGGAGGCTG_GGCTGAGGCTGAGGCGGAGGCGCAGCGGAGGT GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21092481..21092678 26863196 MeRIP-seq:(Medium) rs1225093181 Functional Loss DEL dbSNP153 33..33 33 - - - 104881 RMVar_ID_104881 Human_SNP_ID_547343317 m1A Human chr14 + 21093640 21093640 21093640 CTTTGGTTCTGGGAAGTGCAGGGAAGAGGAGGAAAAGCTGCTAATGAAGGCAACAGGTGCTGTGG CTTTGGTTCTGGGAAGTGCAGGGAAGAGGAGGGAAAGCTGCTAATGAAGGCAACAGGTGCTGTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21093577..21093728 26863196 MeRIP-seq:(Medium) rs1400767408 Functional Loss SNV dbSNP153 33..33 33 - - - 104882 RMVar_ID_104882 Human_SNP_ID_547344396 m1A Human chr14 + 21097879 21097879 21097879 AGAGAGTTTGGGCTCCTTCCCCCTCCCCCACCAGCCCTACCTGGGCCGGGGGTTGGGGGGTGCAC AGAGAGTTTGGGCTCCTTCCCCCTCCCCCACCTGCCCTACCTGGGCCGGGGGTTGGGGGGTGCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21097876..21097965 26863196 MeRIP-seq:(Medium) rs1269634875 Functional Loss SNV dbSNP153 33..33 33 - - - 104883 RMVar_ID_104883 Human_SNP_ID_547344536 m1A Human chr14 - 21098269 21098269 21098269 GCTCCCCCGACTCCCGGGCCCCCCCGTCCGCCACCCGGCCCCCGCCCCCGGCCCCCTCCCCCCTC GCTCCCCCGACTCCCGGGCCCCCCCGTCCGCCCCCCGGCCCCCGCCCCCGGCCCCCTCCCCCCTC T G ZNF219 Ensembl:ENSG00000165804 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21098250..21098414 26863196 MeRIP-seq:(Medium) rs1332797764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26778261 104884 RMVar_ID_104884 Human_SNP_ID_547344601 m1A Human chr14 - 21098388 21098388 21098388 CGGCGCATCTCCCCCGGCCCCACGTAACGCTGACGCCCGCGCCGCCGGCCCGCCGCCCGCCGCCG CGGCGCATCTCCCCCGGCCCCACGTAACGCTGGCGCCCGCGCCGCCGGCCCGCCGCCCGCCGCCG T C ZNF219 Ensembl:ENSG00000165804 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21098293..21098661 26863196 MeRIP-seq:(Medium) rs1011913578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4307815 Human_Splice_Rec_1490539 104885 RMVar_ID_104885 Human_SNP_ID_547344632 m1A Human chr14 - 21098484 21098484 21098484 CGGGCCGCCTCCCGCCGCACACAATGCGGGCCAGGGCCGGGGGCGGGGGACCGGGGAGGGGGCGG CGGGCCGCCTCCCGCCGCACACAATGCGGGCCGGGGCCGGGGGCGGGGGACCGGGGAGGGGGCGG T C ZNF219 Ensembl:ENSG00000165804 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:21098434..21098650 26863196 MeRIP-seq:(Medium) rs965892299 Functional Loss SNV dbSNP153 33..33 33 - - - 104886 RMVar_ID_104886 Human_SNP_ID_547344643 m1A Human chr14 + 21098520 21098520 21098520 CCGCATTGTGTGCGGCGGGAGGCGGCCCGGCCATTAGCATGCGGGGGGCGGCGCGGCGGGGCTGG CCGCATTGTGTGCGGCGGGAGGCGGCCCGGCCTTTAGCATGCGGGGGGCGGCGCGGCGGGGCTGG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:21098433..21098631 26863196 MeRIP-seq:(Medium) rs1344824408 Functional Loss SNV dbSNP153 33..33 33 - - - 104887 RMVar_ID_104887 Human_SNP_ID_547345892 m1A Human chr14 - 21103497 21103497 21103497 AGAAAAGTGCGATGAGGCAAATGTGAAGCTGTATGGGGAGGTGACAGGAAGAGAGGATATGGATG AGAAAAGTGCGATGAGGCAAATGTGAAGCTGTGTGGGGAGGTGACAGGAAGAGAGGATATGGATG T C ZNF219 Ensembl:ENSG00000165804 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21103447..21103667 26863196 MeRIP-seq:(Medium) rs1356588961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4286597,Human_RBP_ID_23615248 104888 RMVar_ID_104888 Human_SNP_ID_547369779 m1A Human chr14 - 21194790 21194786 21194791 AAAGAAAAGAAGGAAGGAAGGAAAAAGAAAGGAAAGAAGAAAACCAGAAAGAAAGGAAGGAAGGA AAAGAAAAGAAGGAAGGAAGGAAAAAGAAAG_____AAGAAAACCAGAAAGAAAGGAAGGAAGGA TCTTTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21194709..21194872 26863196 MeRIP-seq:(Medium) rs1042236395 Functional Loss DEL dbSNP153 32..36 33 - - - 104889 RMVar_ID_104889 Human_SNP_ID_547369796 m1A Human chr14 - 21194824 21194823 21194825 AAAGAAGAGAAGAAGGAAGGAAGGAGAAAGAGAAAAAGAAAAGAAGGAAGGAAGGAAAAAGAAAG AAAGAAGAGAAGAAGGAAGGAAGGAGAAAGA__AAAAGAAAAGAAGGAAGGAAGGAAAAAGAAAG TTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21194737..21194872 26863196 MeRIP-seq:(Medium) rs1287776577 Functional Loss DEL dbSNP153 32..33 33 - - - 104890 RMVar_ID_104890 Human_SNP_ID_547374451 m1A Human chr14 + 21211094 21211094 21211094 CGGGGCAATATGAATTAATGAACATGGGAAGGACAAGGATGGGGAGAACAGTGAGCATGTGCTGA CGGGGCAATATGAATTAATGAACATGGGAAGGGCAAGGATGGGGAGAACAGTGAGCATGTGCTGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21211024..21211150 32194978 MeRIP-seq:(Medium) rs1483695097 Functional Loss SNV dbSNP153 33..33 33 - - - 104891 RMVar_ID_104891 Human_SNP_ID_547374520 m1A Human chr14 - 21211278 21211278 21211278 ACAGCTGGAGTTGATCAAGGATGATGAAAAAGAGGCTGAGGAAGGAGAGGATGACAGAGACAGCG ACAGCTGGAGTTGATCAAGGATGATGAAAAAGGGGCTGAGGAAGGAGAGGATGACAGAGACAGCG T C HNRNPC Ensembl:ENSG00000092199 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs200901083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9368283,Human_RBP_ID_26324807 Human_Splice_Rec_1490696,Human_Splice_Rec_1490708,Human_Splice_Rec_1490724,Human_Splice_Rec_1490736,Human_Splice_Rec_1490750,Human_Splice_Rec_1490780,Human_Splice_Rec_1490796,Human_Splice_Rec_1490810,Human_Splice_Rec_1490824,Human_Splice_Rec_1490836,Human_Splice_Rec_1490852,Human_Splice_Rec_1490856,Human_Splice_Rec_1490870,Human_Splice_Rec_1490886,Human_Splice_Rec_1490900,Human_Splice_Rec_1490920,Human_Splice_Rec_1490932,Human_Splice_Rec_1490948 Human_miRNA_ID_2999173 RMVar_hsa_circ_165137,RMVar_hsa_circ_102923 104892 RMVar_ID_104892 Human_SNP_ID_547374648 m1A Human chr14 - 21211555 21211553 21211556 ACTTGTCCTTCTCATCCGCAGTAGAGATGAAGAATGATAAGTCAGAAGAGGAGCAGAGCAGCAGC ACTTGTCCTTCTCATCCGCAGTAGAGATGAA___TGATAAGTCAGAAGAGGAGCAGAGCAGCAGC ATTC A HNRNPC Ensembl:ENSG00000092199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:21211276..21211608;chr14:21211501..21211575 26863196 MeRIP-seq:(Medium) rs1566590873 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1490698,Human_RBP_ID_1816115,Human_RBP_ID_4286716,Human_RBP_ID_5112289,Human_RBP_ID_6330826,Human_RBP_ID_9039951,Human_RBP_ID_9443988,Human_RBP_ID_12291958,Human_RBP_ID_18160891,Human_RBP_ID_23615382,Human_RBP_ID_24543777,Human_RBP_ID_26324538,Human_RBP_ID_27808657 Human_Splice_Rec_1490678,Human_Splice_Rec_1490694,Human_Splice_Rec_1490722,Human_Splice_Rec_1490734,Human_Splice_Rec_1490748,Human_Splice_Rec_1490764,Human_Splice_Rec_1490778,Human_Splice_Rec_1490794,Human_Splice_Rec_1490808,Human_Splice_Rec_1490822,Human_Splice_Rec_1490834,Human_Splice_Rec_1490854,Human_Splice_Rec_1490868,Human_Splice_Rec_1490884,Human_Splice_Rec_1490898,Human_Splice_Rec_1490918,Human_Splice_Rec_1490930,Human_Splice_Rec_1490946,Human_Splice_Rec_1490964,Human_Splice_Rec_1490968,Human_Splice_Rec_1490974 RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_292410,RMVar_hsa_circ_338118,RMVar_hsa_circ_50653,RMVar_hsa_circ_44097 104893 RMVar_ID_104893 Human_SNP_ID_547374726 m1A Human chr14 - 21211759 21211758 21211759 TGCCCTTGGTATACAGTTGGGTTAGTTACATAAGGCACTTGAAAGTACATGTTGGAATAGTGGAA TGCCCTTGGTATACAGTTGGGTTAGTTACATA_GGCACTTGAAAGTACATGTTGGAATAGTGGAA CT C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21211757..21211919 26863196 MeRIP-seq:(Medium) rs1463995569 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12291962,Human_RBP_ID_17604323,Human_RBP_ID_19066616,Human_RBP_ID_22648248 RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_292410,RMVar_hsa_circ_338118,RMVar_hsa_circ_44097 104894 RMVar_ID_104894 Human_SNP_ID_547374744 m1A Human chr14 - 21211814 21211814 21211814 CTGGAAAAAATTGAAAAGGAACAGAGCAAACAAGCAGGTAAATGGGTTTTCTGCTTGCCCTTGGT CTGGAAAAAATTGAAAAGGAACAGAGCAAACAGGCAGGTAAATGGGTTTTCTGCTTGCCCTTGGT T C HNRNPC Ensembl:ENSG00000092199 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:21211801..21211850 26863196 MeRIP-seq:(Medium) rs17856245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39089,Human_RBP_ID_24543778,Human_RBP_ID_26324539,Human_RBP_ID_27808659 Human_Splice_Rec_1490677,Human_Splice_Rec_1490693,Human_Splice_Rec_1490707,Human_Splice_Rec_1490721,Human_Splice_Rec_1490733,Human_Splice_Rec_1490747,Human_Splice_Rec_1490763,Human_Splice_Rec_1490777,Human_Splice_Rec_1490793,Human_Splice_Rec_1490807,Human_Splice_Rec_1490821,Human_Splice_Rec_1490833,Human_Splice_Rec_1490851,Human_Splice_Rec_1490853,Human_Splice_Rec_1490867,Human_Splice_Rec_1490883,Human_Splice_Rec_1490897,Human_Splice_Rec_1490917,Human_Splice_Rec_1490929,Human_Splice_Rec_1490945,Human_Splice_Rec_1490963,Human_Splice_Rec_1490967,Human_Splice_Rec_1490973 RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_292410,RMVar_hsa_circ_338118,RMVar_hsa_circ_44097,RMVar_hsa_circ_51171,RMVar_hsa_circ_266464,RMVar_hsa_circ_357744 104895 RMVar_ID_104895 Human_SNP_ID_547375098 m1A Human chr14 - 21213001 21213001 21213001 AAACACTTCACGAAGGGGCAAAAGTGGCTTCAATTCTAAGAGTGGACAGCGGGGATCTTCCAAGT AAACACTTCACGAAGGGGCAAAAGTGGCTTCAGTTCTAAGAGTGGACAGCGGGGATCTTCCAAGT T C HNRNPC Ensembl:ENSG00000092199 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21212976..21213000 26863196 MeRIP-seq:(Medium) rs749564993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_119825,Human_RBP_ID_443052,Human_RBP_ID_1490702,Human_RBP_ID_1816120,Human_RBP_ID_6330843,Human_RBP_ID_8401336,Human_RBP_ID_9039953,Human_RBP_ID_9368291,Human_RBP_ID_18647390,Human_RBP_ID_22797376,Human_RBP_ID_26922049,Human_RBP_ID_27225267 Human_Splice_Rec_1490675,Human_Splice_Rec_1490691,Human_Splice_Rec_1490705,Human_Splice_Rec_1490719,Human_Splice_Rec_1490731,Human_Splice_Rec_1490745,Human_Splice_Rec_1490761,Human_Splice_Rec_1490775,Human_Splice_Rec_1490791,Human_Splice_Rec_1490804,Human_Splice_Rec_1490805,Human_Splice_Rec_1490819,Human_Splice_Rec_1490849,Human_Splice_Rec_1490865,Human_Splice_Rec_1490881,Human_Splice_Rec_1490895,Human_Splice_Rec_1490915,Human_Splice_Rec_1490927,Human_Splice_Rec_1490943,Human_Splice_Rec_1490961,Human_Splice_Rec_1490965,Human_Splice_Rec_1490971 RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_292410,RMVar_hsa_circ_338118,RMVar_hsa_circ_110478,RMVar_hsa_circ_44097,RMVar_hsa_circ_51171,RMVar_hsa_circ_266464,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_372680,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730,RMVar_hsa_circ_165140 104896 RMVar_ID_104896 Human_SNP_ID_547381694 m1A Human chr14 - 21234178 21234178 21234178 CCTTACCATCAAACACGATGGCCAGCAACGTTACCAACAAGACAGATCCTCGCTCCATGAACTCC CCTTACCATCAAACACGATGGCCAGCAACGTTTCCAACAAGACAGATCCTCGCTCCATGAACTCC T A HNRNPC Ensembl:ENSG00000092199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21234114..21234276 26863196 MeRIP-seq:(Medium) rs1173002780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443062,Human_RBP_ID_756743,Human_RBP_ID_1171431,Human_RBP_ID_1490751,Human_RBP_ID_1816187,Human_RBP_ID_3443878,Human_RBP_ID_4311009,Human_RBP_ID_6331173,Human_RBP_ID_8401383,Human_RBP_ID_9039973,Human_RBP_ID_12293196,Human_RBP_ID_17248443,Human_RBP_ID_18647428,Human_RBP_ID_22184557,Human_RBP_ID_22439527,Human_RBP_ID_22495256,Human_RBP_ID_22797391,Human_RBP_ID_25125100,Human_RBP_ID_27225279,Human_RBP_ID_27430272 Human_Splice_Rec_1490668,Human_Splice_Rec_1490684,Human_Splice_Rec_1490698,Human_Splice_Rec_1490712,Human_Splice_Rec_1490738,Human_Splice_Rec_1490754,Human_Splice_Rec_1490768,Human_Splice_Rec_1490784,Human_Splice_Rec_1490800,Human_Splice_Rec_1490814,Human_Splice_Rec_1490826,Human_Splice_Rec_1490842,Human_Splice_Rec_1490858,Human_Splice_Rec_1490874,Human_Splice_Rec_1490888,Human_Splice_Rec_1490908,Human_Splice_Rec_1490936,Human_Splice_Rec_1490954,Human_Splice_Rec_1490980,Human_Splice_Rec_1490992,Human_Splice_Rec_1491006,Human_Splice_Rec_1491018,Human_Splice_Rec_1491028,Human_Splice_Rec_1491036,Human_Splice_Rec_1491046,Human_Splice_Rec_1491050 RMVar_hsa_circ_6676,RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_338118,RMVar_hsa_circ_110478,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_307369,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730,RMVar_hsa_circ_362116,RMVar_hsa_circ_294995,RMVar_hsa_circ_270129,RMVar_hsa_circ_61683,RMVar_hsa_circ_165143,RMVar_hsa_circ_165144,RMVar_hsa_circ_165142,RMVar_hsa_circ_165147,RMVar_hsa_circ_92370,RMVar_hsa_circ_333167,RMVar_hsa_circ_165146 104897 RMVar_ID_104897 Human_SNP_ID_547381717 m1A Human chr14 + 21234226 21234226 21234226 CGTGTTTGATGGTAAGGTTTCTCACAAAGCCGAAAACTGTAAAGCAAAAAAAAGTATACAGGTGA CGTGTTTGATGGTAAGGTTTCTCACAAAGCCGCAAACTGTAAAGCAAAAAAAAGTATACAGGTGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21233972..21234794 32194978 MeRIP-seq:(Medium) rs771508728 Functional Loss SNV dbSNP153 33..33 33 - - - 104898 RMVar_ID_104898 Human_SNP_ID_547381718 m1A Human chr14 + 21234226 21234226 21234226 CGTGTTTGATGGTAAGGTTTCTCACAAAGCCGAAAACTGTAAAGCAAAAAAAAGTATACAGGTGA CGTGTTTGATGGTAAGGTTTCTCACAAAGCCGGAAACTGTAAAGCAAAAAAAAGTATACAGGTGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21233972..21234794 32194978 MeRIP-seq:(Medium) rs771508728 Functional Loss SNV dbSNP153 33..33 33 - - - 104899 RMVar_ID_104899 Human_SNP_ID_547383822 m1A Human chr14 - 21241554 21241554 21241554 AGACTTGAAGTGTGTTCAACAACTTAGATCAAATGAAGATCATCCAAGTATGCAGAGGAATTTAT AGACTTGAAGTGTGTTCAACAACTTAGATCAAGTGAAGATCATCCAAGTATGCAGAGGAATTTAT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21241552..21241653 26863196 MeRIP-seq:(Medium) rs1249348453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1490777,Human_RBP_ID_1816236,Human_RBP_ID_12293680,Human_RBP_ID_25087607 RMVar_hsa_circ_6676,RMVar_hsa_circ_44974,RMVar_hsa_circ_110478,RMVar_hsa_circ_307369,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730,RMVar_hsa_circ_294995,RMVar_hsa_circ_165143,RMVar_hsa_circ_165142,RMVar_hsa_circ_165147,RMVar_hsa_circ_92370 104900 RMVar_ID_104900 Human_SNP_ID_547392883 m1A Human chr14 - 21269367 21269364 21269367 CGGTTGTGGCCGCGTTGCCGACCTCCAGCAGCAGTCGGCTTCTCTACGCAGAACCCGGGAGTAGG CGGTTGTGGCCGCGTTGCCGACCTCCAGCAGC___CGGCTTCTCTACGCAGAACCCGGGAGTAGG GACT G HNRNPC Ensembl:ENSG00000092199 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:21269351..21269375 26863196 MeRIP-seq:(Medium) rs1023596000 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1490921,Human_RBP_ID_4308188,Human_RBP_ID_9323722,Human_RBP_ID_9369628,Human_RBP_ID_18417892,Human_RBP_ID_22042814,Human_RBP_ID_22184631,Human_RBP_ID_22438448,Human_RBP_ID_22797448,Human_RBP_ID_23208473,Human_RBP_ID_23615635,Human_RBP_ID_24543781,Human_RBP_ID_26427841,Human_RBP_ID_26922179,Human_RBP_ID_27225310 Human_Splice_Rec_1490667,Human_Splice_Rec_1490679,Human_Splice_Rec_1490697,Human_Splice_Rec_1490709,Human_Splice_Rec_1490751,Human_Splice_Rec_1490765,Human_Splice_Rec_1490781,Human_Splice_Rec_1490797,Human_Splice_Rec_1490811,Human_Splice_Rec_1490825,Human_Splice_Rec_1490837,Human_Splice_Rec_1490857,Human_Splice_Rec_1490871,Human_Splice_Rec_1490901,Human_Splice_Rec_1490933,Human_Splice_Rec_1490949,Human_Splice_Rec_1490975,Human_Splice_Rec_1490987,Human_Splice_Rec_1490999,Human_Splice_Rec_1491013,Human_Splice_Rec_1491033,Human_Splice_Rec_1491039,Human_Splice_Rec_1491047,Human_Splice_Rec_1491051,Human_Splice_Rec_1491055 104901 RMVar_ID_104901 Human_SNP_ID_547392906 m1A Human chr14 + 21269396 21269396 21269396 GACTGCTGCTGGAGGTCGGCAACGCGGCCACAACCGCTCAGTCTTCGTCTCTTCACAAAATGGCC GACTGCTGCTGGAGGTCGGCAACGCGGCCACAGCCGCTCAGTCTTCGTCTCTTCACAAAATGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21269351..21269425 26863196 MeRIP-seq:(Medium) rs956152674 Functional Loss SNV dbSNP153 33..33 33 - - - 104902 RMVar_ID_104902 Human_SNP_ID_547392913 m1A Human chr14 - 21269401 21269401 21269401 TCGGGGGCCATTTTGTGAAGAGACGAAGACTGAGCGGTTGTGGCCGCGTTGCCGACCTCCAGCAG TCGGGGGCCATTTTGTGAAGAGACGAAGACTGGGCGGTTGTGGCCGCGTTGCCGACCTCCAGCAG T C HNRNPC Ensembl:ENSG00000092199 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21269351..21269425 26863196 MeRIP-seq:(Medium) rs754374969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231534,Human_RBP_ID_443082,Human_RBP_ID_758109,Human_RBP_ID_1490921,Human_RBP_ID_4308188,Human_RBP_ID_5418024,Human_RBP_ID_9323723,Human_RBP_ID_9369628,Human_RBP_ID_12295670,Human_RBP_ID_18417892,Human_RBP_ID_22042814,Human_RBP_ID_22184631,Human_RBP_ID_22438448,Human_RBP_ID_23208473,Human_RBP_ID_23615636,Human_RBP_ID_24543781,Human_RBP_ID_26922179,Human_RBP_ID_27225310 104903 RMVar_ID_104903 Human_SNP_ID_547415969 m1A Human chr14 - 21352442 21352442 21352442 CAGATGGCAAGGGAGGAGGTGTTCTTGAAGACAGGAGGAGGCTCCCGCTGTTAATAAATATTGTT CAGATGGCAAGGGAGGAGGTGTTCTTGAAGACCGGAGGAGGCTCCCGCTGTTAATAAATATTGTT T G SUPT16H Ensembl:ENSG00000092201 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21352116..21352500 32194978 MeRIP-seq:(Medium) rs1479298300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39127,Human_RBP_ID_443116,Human_RBP_ID_756753,Human_RBP_ID_1171475,Human_RBP_ID_1816434,Human_RBP_ID_3444085,Human_RBP_ID_6332175,Human_RBP_ID_9368296,Human_RBP_ID_17249027,Human_RBP_ID_17481022,Human_RBP_ID_17846136,Human_RBP_ID_18647575,Human_RBP_ID_21886664 Human_miRNA_ID_2209133,Human_miRNA_ID_3033738 RMVar_hsa_circ_81663,RMVar_hsa_circ_112655,RMVar_hsa_circ_165152,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_165151 104904 RMVar_ID_104904 Human_SNP_ID_547416065 m1A Human chr14 - 21352785 21352783 21352786 GGACCGAGAAAGTCGTTACGAGGAAGAAGAAGAACAAAGTCGAAGTATGAGCCGGAAGAGGAAGG GGACCGAGAAAGTCGTTACGAGGAAGAAGAA___CAAAGTCGAAGTATGAGCCGGAAGAGGAAGG GTTC G SUPT16H Ensembl:ENSG00000092201 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21352735..21353718 26863196 MeRIP-seq:(Medium) rs770668791 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4386,Human_RBP_ID_197289,Human_RBP_ID_883977,Human_RBP_ID_1490959,Human_RBP_ID_1816440,Human_RBP_ID_2408942,Human_RBP_ID_3444090,Human_RBP_ID_3944792,Human_RBP_ID_6332189,Human_RBP_ID_8230457,Human_RBP_ID_8401557,Human_RBP_ID_8793569,Human_RBP_ID_9368300,Human_RBP_ID_12295757,Human_RBP_ID_18160892,Human_RBP_ID_18189464,Human_RBP_ID_18272272,Human_RBP_ID_18435680,Human_RBP_ID_18528236,Human_RBP_ID_18647583,Human_RBP_ID_22926391,Human_RBP_ID_24543783,Human_RBP_ID_25088391,Human_RBP_ID_26324542 Human_Splice_Rec_1491368,Human_Splice_Rec_1491378 Human_miRNA_ID_1132543 RMVar_hsa_circ_81663,RMVar_hsa_circ_112655,RMVar_hsa_circ_165152,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_165151 104905 RMVar_ID_104905 Human_SNP_ID_547416073 m1A Human chr14 - 21352811 21352811 21352811 AACTAATAATGCCTCTTCTATTTAGCGGACCGAGAAAGTCGTTACGAGGAAGAAGAAGAACAAAG AACTAATAATGCCTCTTCTATTTAGCGGACCGGGAAAGTCGTTACGAGGAAGAAGAAGAACAAAG T C SUPT16H Ensembl:ENSG00000092201 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr14:21352718..21352827;chr14:21352526..21353531 26863196,32194978 MeRIP-seq:(Medium) rs752851915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39131,Human_RBP_ID_813787,Human_RBP_ID_880789,Human_RBP_ID_1502497,Human_RBP_ID_1816440,Human_RBP_ID_3944792,Human_RBP_ID_9368301,Human_RBP_ID_12295757,Human_RBP_ID_18189464,Human_RBP_ID_22926391,Human_RBP_ID_24543783,Human_RBP_ID_26324543,Human_RBP_ID_27808103 Human_Splice_Rec_1491368,Human_Splice_Rec_1491378 RMVar_hsa_circ_81663,RMVar_hsa_circ_112655,RMVar_hsa_circ_165152,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_165151 104906 RMVar_ID_104906 Human_SNP_ID_547416225 m1A Human chr14 + 21353440 21353440 21353440 TACTAACACCTCAAAATATTGAAATGTGTTAGAAATTTGTGCGTAGACAAATGAATAAAAAACAA TACTAACACCTCAAAATATTGAAATGTGTTAGGAATTTGTGCGTAGACAAATGAATAAAAAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21353438..21353591 26863196 MeRIP-seq:(Medium) rs987228057 Functional Loss SNV dbSNP153 33..33 33 - - - 104907 RMVar_ID_104907 Human_SNP_ID_547417297 m1A Human chr14 + 21357343 21357343 21357343 TGGACCCGCTCAAAGTGGATCAGCTCTACCTCATCCAATGTCACCACAAAAGGTGGCTGTCAGGG TGGACCCGCTCAAAGTGGATCAGCTCTACCTCGTCCAATGTCACCACAAAAGGTGGCTGTCAGGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21357293..21358003 32194978 MeRIP-seq:(Medium) rs1256940145 Functional Loss SNV dbSNP153 33..33 33 - - - 104908 RMVar_ID_104908 Human_SNP_ID_547418947 m1A Human chr14 + 21363320 21363320 21363320 GCCTCATCTTTCTCCTCCTCCTCTTCTTCCTCATCTTCATTCTATGGAAAAAGTCATAATCAAAA GCCTCATCTTTCTCCTCCTCCTCTTCTTCCTCGTCTTCATTCTATGGAAAAAGTCATAATCAAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21363307..21363450 26863196 MeRIP-seq:(Medium) rs1274332025 Functional Loss SNV dbSNP153 33..33 33 - - - 104909 RMVar_ID_104909 Human_SNP_ID_547418990 m1A Human chr14 - 21363428 21363425 21363428 AGAATGTGGGGATTTTCCTAAAGGTAGGAAGAAGATAGATAAGTAGTATAGGAAGTTTAGGATAT AGAATGTGGGGATTTTCCTAAAGGTAGGAAGA___TAGATAAGTAGTATAGGAAGTTTAGGATAT ATCT A SUPT16H Ensembl:ENSG00000092201 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21363426..21363475 26863196 MeRIP-seq:(Medium) rs751773282 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_19064635 Human_Splice_Rec_1491338 RMVar_hsa_circ_5128,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_324911,RMVar_hsa_circ_319139,RMVar_hsa_circ_88784,RMVar_hsa_circ_56697,RMVar_hsa_circ_69827,RMVar_hsa_circ_77409,RMVar_hsa_circ_165159,RMVar_hsa_circ_165160,RMVar_hsa_circ_64906,RMVar_hsa_circ_165161,RMVar_hsa_circ_44629,RMVar_hsa_circ_69099,RMVar_hsa_circ_25828,RMVar_hsa_circ_105804,RMVar_hsa_circ_70524,RMVar_hsa_circ_35762,RMVar_hsa_circ_165166 104910 RMVar_ID_104910 Human_SNP_ID_547419005 m1A Human chr14 + 21363501 21363501 21363501 TTCTTCACAGAAGTGAGAACAGTAGCTGGGCCATCCTAGAATTAAAAGGAGAATGAAGACACATT TTCTTCACAGAAGTGAGAACAGTAGCTGGGCCGTCCTAGAATTAAAAGGAGAATGAAGACACATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21363450..21364873 32194978 MeRIP-seq:(Medium) rs759296800 Functional Loss SNV dbSNP153 33..33 33 - - - 104911 RMVar_ID_104911 Human_SNP_ID_547421613 m1A Human chr14 - 21373425 21373423 21373426 TAAGTGATGATTACCCACTCTTTTCAGAAAGGAGAAGATGAGTATGCCAACGTTGATGCCATTGT TAAGTGATGATTACCCACTCTTTTCAGAAAG___AAGATGAGTATGCCAACGTTGATGCCATTGT TCTC T SUPT16H Ensembl:ENSG00000092201 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21373376..21373479 26863196 MeRIP-seq:(Medium) rs757660683 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_883897,Human_RBP_ID_2408975,Human_RBP_ID_9368361,Human_RBP_ID_26324555,Human_RBP_ID_27808675 Human_Splice_Rec_1491320,Human_Splice_Rec_1491321,Human_Splice_Rec_1491384,Human_Splice_Rec_1491385,Human_Splice_Rec_1491394,Human_Splice_Rec_1491395,Human_Splice_Rec_1491402,Human_Splice_Rec_1491403,Human_Splice_Rec_1491412,Human_Splice_Rec_1491413 RMVar_hsa_circ_319139,RMVar_hsa_circ_88784,RMVar_hsa_circ_56697,RMVar_hsa_circ_165160,RMVar_hsa_circ_332039,RMVar_hsa_circ_101972,RMVar_hsa_circ_14893,RMVar_hsa_circ_364753,RMVar_hsa_circ_165170,RMVar_hsa_circ_364627,RMVar_hsa_circ_165169,RMVar_hsa_circ_276508 104912 RMVar_ID_104912 Human_SNP_ID_547424441 m1A Human chr14 + 21383959 21383959 21383959 TAGCCCCGGACGCCGCTTCTCCTCGGGTTCCGAGAATCACGCGAGGTCCCGGCTCAGCCACCCGC TAGCCCCGGACGCCGCTTCTCCTCGGGTTCCGCGAATCACGCGAGGTCCCGGCTCAGCCACCCGC A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:21383876..21384025 26863410 MeRIP-seq:(Medium) rs754830939 Functional Loss SNV dbSNP153 33..33 33 - - - 104913 RMVar_ID_104913 Human_SNP_ID_547424443 m1A Human chr14 - 21383963 21383963 21383963 GAGAGCGGGTGGCTGAGCCGGGACCTCGCGTGATTCTCGGAACCCGAGGAGAAGCGGCGTCCGGG GAGAGCGGGTGGCTGAGCCGGGACCTCGCGTGGTTCTCGGAACCCGAGGAGAAGCGGCGTCCGGG T C SUPT16H Ensembl:ENSG00000092201 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972533,GSM1972534 HEK293T cell line,total RNA;HEPG2 cell line,total RNA Untreated chr14:21383851..21384025 26863196 MeRIP-seq:(Medium) rs370039379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230968,Human_RBP_ID_813798,Human_RBP_ID_1491094,Human_RBP_ID_1816516,Human_RBP_ID_4286988,Human_RBP_ID_5438910,Human_RBP_ID_5493352,Human_RBP_ID_8793614,Human_RBP_ID_9282137,Human_RBP_ID_9368364,Human_RBP_ID_17846155,Human_RBP_ID_18417893,Human_RBP_ID_18647661,Human_RBP_ID_18980109,Human_RBP_ID_22439022,Human_RBP_ID_23615688,Human_RBP_ID_26324558 RMVar_hsa_circ_88784,RMVar_hsa_circ_165160 104914 RMVar_ID_104914 Human_SNP_ID_547424444 m1A Human chr14 + 21383965 21383965 21383965 CGGACGCCGCTTCTCCTCGGGTTCCGAGAATCACGCGAGGTCCCGGCTCAGCCACCCGCTCTCGG CGGACGCCGCTTCTCCTCGGGTTCCGAGAATCGCGCGAGGTCCCGGCTCAGCCACCCGCTCTCGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:21383876..21384025 26863410 MeRIP-seq:(Medium) rs373795558 Functional Loss SNV dbSNP153 33..33 33 - - - 104915 RMVar_ID_104915 Human_SNP_ID_547424921 m1A Human chr14 + 21385343 21385343 21385343 CGCTACATAGTCTGTGGTTAATGGAGGTGACTAGGGAGGGGTGAGCACACCAGCTGCTCTAGTCT CGCTACATAGTCTGTGGTTAATGGAGGTGACTTGGGAGGGGTGAGCACACCAGCTGCTCTAGTCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21385293..21385493 32194978 MeRIP-seq:(Medium) rs898246870 Functional Loss SNV dbSNP153 33..33 33 - - - 104916 RMVar_ID_104916 Human_SNP_ID_547427425 m1A Human chr14 + 21393756 21393756 21393756 AAAGTCAGACTCTCCAGACTGGGGACCTGGGTAGCTGTCTCCTCGGGTGACTTTTCAACAGGAGC AAAGTCAGACTCTCCAGACTGGGGACCTGGGTGGCTGTCTCCTCGGGTGACTTTTCAACAGGAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21393707..21393778 26863196 MeRIP-seq:(Medium) rs1216296900 Functional Loss SNV dbSNP153 33..33 33 - - - 104917 RMVar_ID_104917 Human_SNP_ID_547436466 m1A Human chr14 - 21427969 21427969 21427969 CCAGCGTTCGGCCAGAGGAGGAAGGCGAGAAGAAACGCAGGAAGAAGAGTGCTGGGGAGAGGCTG CCAGCGTTCGGCCAGAGGAGGAAGGCGAGAAGTAACGCAGGAAGAAGAGTGCTGGGGAGAGGCTG T A CHD8 Ensembl:ENSG00000100888 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21427919..21428100 26863196 MeRIP-seq:(Medium) rs1555318020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39483,Human_RBP_ID_881479,Human_RBP_ID_6332543,Human_RBP_ID_24543641,Human_RBP_ID_26324867,Human_RBP_ID_27808680 RMVar_hsa_circ_112099,RMVar_hsa_circ_165171,RMVar_hsa_circ_165189,RMVar_hsa_circ_357510,RMVar_hsa_circ_55742,RMVar_hsa_circ_18830,RMVar_hsa_circ_165198,RMVar_hsa_circ_320559,RMVar_hsa_circ_72968,RMVar_hsa_circ_58078,RMVar_hsa_circ_295805,RMVar_hsa_circ_68831,RMVar_hsa_circ_165201,RMVar_hsa_circ_90288,RMVar_hsa_circ_275543,RMVar_hsa_circ_165203,RMVar_hsa_circ_165202,RMVar_hsa_circ_310019 104918 RMVar_ID_104918 Human_SNP_ID_547438932 m1A Human chr14 + 21437132 21437132 21437132 GTTAGGGCGGAAGCTGCAGGCCGAGAGGCCCGACAAGCCCTGAAGGAGAAAACGAGCTGTGCCTC GTTAGGGCGGAAGCTGCAGGCCGAGAGGCCCGGCAAGCCCTGAAGGAGAAAACGAGCTGTGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21437129..21437216 26863196 MeRIP-seq:(Medium) rs1218490676 Functional Loss SNV dbSNP153 33..33 33 - - - 104919 RMVar_ID_104919 Human_SNP_ID_547445454 m1A Human chr14 - 21460473 21460473 21460473 TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCACACCTG TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTGGCTGGGACTACAGGCATGTGCCACCACACCTG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1207441763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 104920 RMVar_ID_104920 Human_SNP_ID_547445472 m1A Human chr14 - 21460522 21460522 21460522 GGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAGTTCTCCTG GGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCTCCACTTTCCAGGTTCAAGCAGTTCTCCTG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1419364886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 104921 RMVar_ID_104921 Human_SNP_ID_547449722 m1A Human chr14 + 21476598 21476598 21476598 GTAAACTGCAGGAGGAGACATGACTTCCCCACACCTGAAAGAGAAAGCACACTCCCGGAATCACG GTAAACTGCAGGAGGAGACATGACTTCCCCACGCCTGAAAGAGAAAGCACACTCCCGGAATCACG A G TOX4 Ensembl:ENSG00000092203 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21476572..21476973 26863196 MeRIP-seq:(Medium) rs1303449090 Functional Loss SNV dbSNP153 33..33 33 - - - 104922 RMVar_ID_104922 Human_SNP_ID_547449902 m1A Human chr14 - 21476887 21476887 21476887 GTGGCTATAGAAGTCGGGCGGACCCGGAACCCAGAGGACGCGACACCATGACTTATGCTTATCTC GTGGCTATAGAAGTCGGGCGGACCCGGAACCCGGAGGACGCGACACCATGACTTATGCTTATCTC T C RAB2B Ensembl:ENSG00000129472 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21476837..21476959 26863196 MeRIP-seq:(Medium) rs936673874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944799,Human_RBP_ID_9369683,Human_RBP_ID_18417895 Human_Splice_Rec_1492149,Human_Splice_Rec_1492163,Human_Splice_Rec_1492177,Human_Splice_Rec_1492199,Human_Splice_Rec_1492203 104923 RMVar_ID_104923 Human_SNP_ID_547452526 m1A Human chr14 - 21487412 21487412 21487412 GGGAAAAAAGGGGGAAAAGAATTAGTGAAAAGAGGAGAAATGGCATACTACTAAGTGAAGAACAT GGGAAAAAAGGGGGAAAAGAATTAGTGAAAAGGGGAGAAATGGCATACTACTAAGTGAAGAACAT T C lnc-SALL2-2,RF00017-1500 RNACentral:URS00008B947C,RNACentral:URS00009030E0 lincRNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:21487407..21487502 26863196 MeRIP-seq:(Medium) rs768815558 Functional Loss SNV dbSNP153 33..33 33 - - - 104924 RMVar_ID_104924 Human_SNP_ID_547452528 m1A Human chr14 - 21487416 21487416 21487416 GTAGGGGAAAAAAGGGGGAAAAGAATTAGTGAAAAGAGGAGAAATGGCATACTACTAAGTGAAGA GTAGGGGAAAAAAGGGGGAAAAGAATTAGTGACAAGAGGAGAAATGGCATACTACTAAGTGAAGA T G lnc-SALL2-2,RF00017-1500 RNACentral:URS00008B947C,RNACentral:URS00009030E0 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:21487412..21487553 26863196 MeRIP-seq:(Medium) rs985130433 Functional Loss SNV dbSNP153 33..33 33 - - - 104925 RMVar_ID_104925 Human_SNP_ID_547452868 m1A Human chr14 - 21488748 21488748 21488748 TCAGGTGACTGGGCAGGTGGCAGGATGGTGCCACCCCCTAGGCTCAAACCCAGCTGGGAACTCAG TCAGGTGACTGGGCAGGTGGCAGGATGGTGCCGCCCCCTAGGCTCAAACCCAGCTGGGAACTCAG T C lnc-SALL2-2,RF00017-1500 RNACentral:URS00008B947C,RNACentral:URS00009030E0 lincRNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21488651..21488750 32194978 MeRIP-seq:(Medium) rs748794981 Functional Loss SNV dbSNP153 33..33 33 - - - 104926 RMVar_ID_104926 Human_SNP_ID_547454060 m1A Human chr14 + 21493064 21493064 21493064 GCAACAGCCTCCACCTCAGAAAGTTCGAATCAATTTACAGCAACAGCCTCCTCCTCTGCAGATCA GCAACAGCCTCCACCTCAGAAAGTTCGAATCAGTTTACAGCAACAGCCTCCTCCTCTGCAGATCA A G TOX4 Ensembl:ENSG00000092203 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:21493026..21493100 26863196 MeRIP-seq:(Medium) rs751970253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18980123,Human_RBP_ID_26922431 Human_miRNA_ID_1394787,Human_miRNA_ID_2715126,Human_miRNA_ID_3051109 RMVar_hsa_circ_165211,RMVar_hsa_circ_370024 104927 RMVar_ID_104927 Human_SNP_ID_547454740 m1A Human chr14 - 21495303 21495303 21495303 ACAATGGGAGGGTTCTCACAACCAGACCTCACACATCGAGGCTGGGGTGAGAGTGCCACAGGAGA ACAATGGGAGGGTTCTCACAACCAGACCTCACCCATCGAGGCTGGGGTGAGAGTGCCACAGGAGA T G lnc-SALL2-2,RF00017-1500 RNACentral:URS00008B947C,RNACentral:URS00009030E0 lincRNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21493190..21495362 32194978 MeRIP-seq:(Medium) rs1391717620 Functional Loss SNV dbSNP153 33..33 33 - - - 104928 RMVar_ID_104928 Human_SNP_ID_547456008 m1A Human chr14 - 21499552 21499552 21499552 GAAATTATTTGGGTGAAGACAAATCAACTGCAACGCATCATTCGGACAGGCCGTACAGGTCACTG GAAATTATTTGGGTGAAGACAAATCAACTGCAGCGCATCATTCGGACAGGCCGTACAGGTCACTG T C METTL3 Ensembl:ENSG00000165819 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21499457..21499577 26863196 MeRIP-seq:(Medium) rs569532008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1816688,Human_RBP_ID_3944801,Human_RBP_ID_8401725,Human_RBP_ID_12297776,Human_RBP_ID_18206849,Human_RBP_ID_18435697,Human_RBP_ID_18528266,Human_RBP_ID_18979187,Human_RBP_ID_22184814,Human_RBP_ID_22922337,Human_RBP_ID_23208476 Human_Splice_Rec_1492332,Human_Splice_Rec_1492333,Human_Splice_Rec_1492350,Human_Splice_Rec_1492351,Human_Splice_Rec_1492366,Human_Splice_Rec_1492367,Human_Splice_Rec_1492378,Human_Splice_Rec_1492396,Human_Splice_Rec_1492412,Human_Splice_Rec_1492426,Human_Splice_Rec_1492427 RMVar_hsa_circ_32592,RMVar_hsa_circ_126379,RMVar_hsa_circ_45235,RMVar_hsa_circ_165213 104929 RMVar_ID_104929 Human_SNP_ID_547456012 m1A Human chr14 + 21499577 21499577 21499577 TGATGCGTTGCAGTTGATTTGTCTTCACCCAAATAATTTCATCTACCCGTTCATACCTGTGGGGC TGATGCGTTGCAGTTGATTTGTCTTCACCCAAGTAATTTCATCTACCCGTTCATACCTGTGGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21499526..21499625 26863196 MeRIP-seq:(Medium) rs774309591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3444337,Human_RBP_ID_17246846,Human_RBP_ID_17846251 104930 RMVar_ID_104930 Human_SNP_ID_547457062 m1A Human chr14 + 21503426 21503426 21503426 CCCCAGGGCCCTTCTTTTCTGCCACAGCACCCATCATGGCAGAGAGCTTGGAATGGTCAGCATAG CCCCAGGGCCCTTCTTTTCTGCCACAGCACCCGTCATGGCAGAGAGCTTGGAATGGTCAGCATAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:21503376..21503425 32194978 MeRIP-seq:(Medium) rs146042078 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 104931 RMVar_ID_104931 Human_SNP_ID_547459070 m1A Human chr14 + 21511280 21511280 21511280 CTCGAATAAGGCGCGGCGGACTAGCACCTCCCAGCACTCGCTCCAGGATATAGCCAATTCTCACG CTCGAATAAGGCGCGGCGGACTAGCACCTCCCGGCACTCGCTCCAGGATATAGCCAATTCTCACG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21511101..21511325 26863196 MeRIP-seq:(Medium) rs1434231398 Functional Loss SNV dbSNP153 33..33 33 - - - 104932 RMVar_ID_104932 Human_SNP_ID_547461836 m1A Human chr14 - 21522265 21522265 21522265 TCTGGGGTGACCTTTCTGCTCAGCTGGTGGGTATGGGTCCCCTATCTTTCTAGAACCAGTATGTG TCTGGGGTGACCTTTCTGCTCAGCTGGTGGGTGTGGGTCCCCTATCTTTCTAGAACCAGTATGTG T C SALL2 Ensembl:ENSG00000165821 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:21522214..21522314 32194978 MeRIP-seq:(Medium) rs1377119859 Functional Loss SNV dbSNP153 33..33 33 - - - 104933 RMVar_ID_104933 Human_SNP_ID_547463357 m1A Human chr14 - 21526252 21526252 21526252 TCCGCCGCTGCTCCCTGCCCCCGCCGCTGCCGATCTCCATCTCCGCAGTCTGGGCCGCTGGGTGC TCCGCCGCTGCTCCCTGCCCCCGCCGCTGCCGGTCTCCATCTCCGCAGTCTGGGCCGCTGGGTGC T C SALL2 Ensembl:ENSG00000165821 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:21526161..21526255 26863410 MeRIP-seq:(Medium) rs1025280867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5127676,Human_RBP_ID_18937160 104934 RMVar_ID_104934 Human_SNP_ID_547746459 m1A Human chr14 - 22589161 22589161 22589161 GTTTGGGGCGCGGACCGGAGTACCTTGCGTGCAGTTATGTCGGCGTCGGTAGTGTCTGTCATTTC GTTTGGGGCGCGGACCGGAGTACCTTGCGTGCGGTTATGTCGGCGTCGGTAGTGTCTGTCATTTC T C DAD1 Ensembl:ENSG00000129562 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:22564999..22589200 32194978 MeRIP-seq:(Medium) rs1180103701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39808,Human_RBP_ID_443350,Human_RBP_ID_1491316,Human_RBP_ID_3444438,Human_RBP_ID_4287670,Human_RBP_ID_5141049,Human_RBP_ID_9324009,Human_RBP_ID_12298770,Human_RBP_ID_23615986,Human_RBP_ID_27430426 104935 RMVar_ID_104935 Human_SNP_ID_547746472 m1A Human chr14 - 22589172 22589172 22589172 GTCCTCCAAGAGTTTGGGGCGCGGACCGGAGTACCTTGCGTGCAGTTATGTCGGCGTCGGTAGTG GTCCTCCAAGAGTTTGGGGCGCGGACCGGAGTGCCTTGCGTGCAGTTATGTCGGCGTCGGTAGTG T C DAD1 Ensembl:ENSG00000129562 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:22588989..22589225;chr14:22589126..22589200;chr14:22589010..22589225;chr14:22589061..22589225;chr14:22589071..22589225 26863196 MeRIP-seq:(Medium) rs139670797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39808,Human_RBP_ID_230825,Human_RBP_ID_443350,Human_RBP_ID_1491316,Human_RBP_ID_4287670,Human_RBP_ID_5141049,Human_RBP_ID_5418035,Human_RBP_ID_5463236,Human_RBP_ID_9040094,Human_RBP_ID_9324009,Human_RBP_ID_12298771,Human_RBP_ID_23615986,Human_RBP_ID_26427901,Human_RBP_ID_27430426 104936 RMVar_ID_104936 Human_SNP_ID_547761171 m1A Human chr14 + 22640384 22640384 22640384 GAGGAAGGAAGGGGGAAAAAAGAGAAGGAGGGAACAGTGTCCAAAGACAGGAGAATAAATCATGA GAGGAAGGAAGGGGGAAAAAAGAGAAGGAGGGTACAGTGTCCAAAGACAGGAGAATAAATCATGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:22640328..22640415 26863196 MeRIP-seq:(Medium) rs1045516246 Functional Loss SNV dbSNP153 33..33 33 - - - 104937 RMVar_ID_104937 Human_SNP_ID_547761631 m1A Human chr14 + 22641362 22641361 22641362 GAAGAAAGGAGGGAGGGAGGGAAGAAAGAAAGAAAGGGGGGAGAGAAGAAAGAAAGAGAGAGAGA GAAGAAAGGAGGGAGGGAGGGAAGAAAGAAAG_AAGGGGGGAGAGAAGAAAGAAAGAGAGAGAGA GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:22641262..22641407 26863196 MeRIP-seq:(Medium) rs1461802916 Functional Loss DEL dbSNP153 33..33 33 - - - 104938 RMVar_ID_104938 Human_SNP_ID_547761632 m1A Human chr14 + 22641362 22641362 22641362 GAAGAAAGGAGGGAGGGAGGGAAGAAAGAAAGAAAGGGGGGAGAGAAGAAAGAAAGAGAGAGAGA GAAGAAAGGAGGGAGGGAGGGAAGAAAGAAAGGAAGGGGGGAGAGAAGAAAGAAAGAGAGAGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:22641262..22641407 26863196 MeRIP-seq:(Medium) rs60114342 Functional Loss SNV dbSNP153 33..33 33 - - - 104939 RMVar_ID_104939 Human_SNP_ID_547792709 m1A Human chr14 + 22766708 22766708 22766708 CAAAAGCAAGTCCTCTTCCGGGCAAAATGGCGATGGGACTAATGTGCGGACGCCGGGAGCTTCTG CAAAAGCAAGTCCTCTTCCGGGCAAAATGGCGGTGGGACTAATGTGCGGACGCCGGGAGCTTCTG A G OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs562492559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443370,Human_RBP_ID_1491329,Human_RBP_ID_4308198,Human_RBP_ID_5140719,Human_RBP_ID_9323725,Human_RBP_ID_12298809,Human_RBP_ID_23616010 Human_Splice_Rec_1492827,Human_Splice_Rec_1492845,Human_Splice_Rec_1492849,Human_Splice_Rec_1492851,Human_Splice_Rec_1492857,Human_Splice_Rec_1492875,Human_Splice_Rec_1492895,Human_Splice_Rec_1492911 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680 104940 RMVar_ID_104940 Human_SNP_ID_547792710 m1A Human chr14 + 22766708 22766708 22766708 CAAAAGCAAGTCCTCTTCCGGGCAAAATGGCGATGGGACTAATGTGCGGACGCCGGGAGCTTCTG CAAAAGCAAGTCCTCTTCCGGGCAAAATGGCGTTGGGACTAATGTGCGGACGCCGGGAGCTTCTG A T OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs562492559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443370,Human_RBP_ID_1491329,Human_RBP_ID_4308198,Human_RBP_ID_5140719,Human_RBP_ID_9323725,Human_RBP_ID_12298809,Human_RBP_ID_23616010 Human_Splice_Rec_1492827,Human_Splice_Rec_1492845,Human_Splice_Rec_1492849,Human_Splice_Rec_1492851,Human_Splice_Rec_1492857,Human_Splice_Rec_1492875,Human_Splice_Rec_1492895,Human_Splice_Rec_1492911 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680 104941 RMVar_ID_104941 Human_SNP_ID_547792762 m1A Human chr14 + 22766751 22766751 22766751 GTGCGGACGCCGGGAGCTTCTGCGCTTGCTACAGTCCGGGCGTCGGGTAAGGATGCCCCGGGGCA GTGCGGACGCCGGGAGCTTCTGCGCTTGCTACGGTCCGGGCGTCGGGTAAGGATGCCCCGGGGCA A G OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:22766701..22766775 26863196 MeRIP-seq:(Medium) rs1227034023 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_757257,Human_RBP_ID_813655,Human_RBP_ID_883680,Human_RBP_ID_4308198,Human_RBP_ID_5140719,Human_RBP_ID_5352673,Human_RBP_ID_9323725,Human_RBP_ID_18417898,Human_RBP_ID_19063630,Human_RBP_ID_22044436 Human_Splice_Rec_1492827,Human_Splice_Rec_1492845,Human_Splice_Rec_1492849,Human_Splice_Rec_1492851,Human_Splice_Rec_1492857,Human_Splice_Rec_1492875,Human_Splice_Rec_1492895,Human_Splice_Rec_1492911 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680 104942 RMVar_ID_104942 Human_SNP_ID_547793065 m1A Human chr14 + 22767337 22767337 22767337 CTATTCCCAGCAGCCCCGTGCTGCTGTCGCCCACACTACCTCTTCCTTGCGGCTTCCGGCCCCCG CTATTCCCAGCAGCCCCGTGCTGCTGTCGCCCCCACTACCTCTTCCTTGCGGCTTCCGGCCCCCG A C OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22767226..22767378 26863196 MeRIP-seq:(Medium) rs141437641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231250,Human_RBP_ID_1171542,Human_RBP_ID_4311306,Human_RBP_ID_5493372,Human_RBP_ID_9323726,Human_RBP_ID_17481024,Human_RBP_ID_22797513,Human_RBP_ID_24471087,Human_RBP_ID_27430438 Human_Splice_Rec_1492828,Human_Splice_Rec_1492829,Human_Splice_Rec_1492846,Human_Splice_Rec_1492847,Human_Splice_Rec_1492850,Human_Splice_Rec_1492852,Human_Splice_Rec_1492853,Human_Splice_Rec_1492858,Human_Splice_Rec_1492859,Human_Splice_Rec_1492876,Human_Splice_Rec_1492877,Human_Splice_Rec_1492886,Human_Splice_Rec_1492887,Human_Splice_Rec_1492896,Human_Splice_Rec_1492897,Human_Splice_Rec_1492912,Human_Splice_Rec_1492913,Human_Splice_Rec_1492928,Human_Splice_Rec_1492929,Human_Splice_Rec_1492946,Human_Splice_Rec_1492947,Human_Splice_Rec_1492949 Human_miRNA_ID_1131,Human_miRNA_ID_4786,Human_miRNA_ID_8447,Human_miRNA_ID_11977,Human_miRNA_ID_15550,Human_miRNA_ID_19203,Human_miRNA_ID_22839,Human_miRNA_ID_26489,Human_miRNA_ID_490969,Human_miRNA_ID_494226,Human_miRNA_ID_1914641,Human_miRNA_ID_1917090,Human_miRNA_ID_1919542,Human_miRNA_ID_1921999,Human_miRNA_ID_1924454,Human_miRNA_ID_1926905,Human_miRNA_ID_1929356,Human_miRNA_ID_1931809,Human_miRNA_ID_2061584,Human_miRNA_ID_2168580,Human_miRNA_ID_2170104,Human_miRNA_ID_2629637,Human_miRNA_ID_2642751,Human_miRNA_ID_3125491 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680,RMVar_hsa_circ_125634,RMVar_hsa_circ_165221 104943 RMVar_ID_104943 Human_SNP_ID_547793066 m1A Human chr14 + 22767337 22767337 22767337 CTATTCCCAGCAGCCCCGTGCTGCTGTCGCCCACACTACCTCTTCCTTGCGGCTTCCGGCCCCCG CTATTCCCAGCAGCCCCGTGCTGCTGTCGCCCTCACTACCTCTTCCTTGCGGCTTCCGGCCCCCG A T OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22767226..22767378 26863196 MeRIP-seq:(Medium) rs141437641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231250,Human_RBP_ID_1171542,Human_RBP_ID_4311306,Human_RBP_ID_5493372,Human_RBP_ID_9323726,Human_RBP_ID_17481024,Human_RBP_ID_22797513,Human_RBP_ID_24471087,Human_RBP_ID_27430438 Human_Splice_Rec_1492828,Human_Splice_Rec_1492829,Human_Splice_Rec_1492846,Human_Splice_Rec_1492847,Human_Splice_Rec_1492850,Human_Splice_Rec_1492852,Human_Splice_Rec_1492853,Human_Splice_Rec_1492858,Human_Splice_Rec_1492859,Human_Splice_Rec_1492876,Human_Splice_Rec_1492877,Human_Splice_Rec_1492886,Human_Splice_Rec_1492887,Human_Splice_Rec_1492896,Human_Splice_Rec_1492897,Human_Splice_Rec_1492912,Human_Splice_Rec_1492913,Human_Splice_Rec_1492928,Human_Splice_Rec_1492929,Human_Splice_Rec_1492946,Human_Splice_Rec_1492947,Human_Splice_Rec_1492949 Human_miRNA_ID_1131,Human_miRNA_ID_4786,Human_miRNA_ID_8447,Human_miRNA_ID_11977,Human_miRNA_ID_15550,Human_miRNA_ID_19203,Human_miRNA_ID_22839,Human_miRNA_ID_26489,Human_miRNA_ID_490969,Human_miRNA_ID_494226,Human_miRNA_ID_1914641,Human_miRNA_ID_1917090,Human_miRNA_ID_1919542,Human_miRNA_ID_1921999,Human_miRNA_ID_1924454,Human_miRNA_ID_1926905,Human_miRNA_ID_1929356,Human_miRNA_ID_1931809,Human_miRNA_ID_2061584,Human_miRNA_ID_2168580,Human_miRNA_ID_2170104,Human_miRNA_ID_2629637,Human_miRNA_ID_2642751,Human_miRNA_ID_3125491 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680,RMVar_hsa_circ_125634,RMVar_hsa_circ_165221 104944 RMVar_ID_104944 Human_SNP_ID_547810875 m1A Human chr14 + 22829928 22829928 22829928 GGCTACTCCTGCTCAGCATGGCTGCTTTAGGGACTGTTCTCTTCAGTGAGTGGGTATAGATAGGG GGCTACTCCTGCTCAGCATGGCTGCTTTAGGGGCTGTTCTCTTCAGTGAGTGGGTATAGATAGGG A G MRPL52 Ensembl:ENSG00000172590 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs372433571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443424,Human_RBP_ID_1171545,Human_RBP_ID_1491362,Human_RBP_ID_4308199,Human_RBP_ID_12298994,Human_RBP_ID_19064698,Human_RBP_ID_22439535 Human_Splice_Rec_1493191,Human_Splice_Rec_1493195,Human_Splice_Rec_1493205,Human_Splice_Rec_1493209,Human_Splice_Rec_1493215,Human_Splice_Rec_1493229,Human_Splice_Rec_1493245,Human_Splice_Rec_1493251,Human_Splice_Rec_1493261,Human_Splice_Rec_1493269 104945 RMVar_ID_104945 Human_SNP_ID_547810999 m1A Human chr14 + 22830203 22830203 22830203 GTTTTTCTCCACACAGGCAGGGACTGGCTGCCAACCCCTCCGGCTACGGGCCCCTTACCGAGCTC GTTTTTCTCCACACAGGCAGGGACTGGCTGCCCACCCCTCCGGCTACGGGCCCCTTACCGAGCTC A C MRPL52 Ensembl:ENSG00000172590 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22830051..22830301 26863196 MeRIP-seq:(Medium) rs1485241316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443428,Human_RBP_ID_757773,Human_RBP_ID_4308201,Human_RBP_ID_5351326,Human_RBP_ID_5418038,Human_RBP_ID_5463239,Human_RBP_ID_5493374,Human_RBP_ID_8793851,Human_RBP_ID_17651297,Human_RBP_ID_17846362,Human_RBP_ID_19063637,Human_RBP_ID_22438460,Human_RBP_ID_22539815,Human_RBP_ID_23616038,Human_RBP_ID_26922525,Human_RBP_ID_27225544 Human_Splice_Rec_1493194,Human_Splice_Rec_1493198,Human_Splice_Rec_1493199,Human_Splice_Rec_1493204,Human_Splice_Rec_1493208,Human_Splice_Rec_1493210,Human_Splice_Rec_1493211,Human_Splice_Rec_1493218,Human_Splice_Rec_1493219,Human_Splice_Rec_1493224,Human_Splice_Rec_1493225,Human_Splice_Rec_1493232,Human_Splice_Rec_1493233,Human_Splice_Rec_1493238,Human_Splice_Rec_1493239,Human_Splice_Rec_1493248,Human_Splice_Rec_1493249,Human_Splice_Rec_1493254,Human_Splice_Rec_1493255,Human_Splice_Rec_1493258,Human_Splice_Rec_1493259,Human_Splice_Rec_1493264,Human_Splice_Rec_1493265,Human_Splice_Rec_1493272,Human_Splice_Rec_1493273,Human_Splice_Rec_1493278,Human_Splice_Rec_1493279,Human_Splice_Rec_1493284,Human_Splice_Rec_1493285 104946 RMVar_ID_104946 Human_SNP_ID_547811024 m1A Human chr14 - 22830250 22830250 22830250 TGGAGTTAACTGCCAGATCAGCGCTTACCCGCATATGACCAGTCTGGGAGCTCGGTAAGGGGCCC TGGAGTTAACTGCCAGATCAGCGCTTACCCGCGTATGACCAGTCTGGGAGCTCGGTAAGGGGCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:22830226..22830250 26863196 MeRIP-seq:(Medium) rs757364045 Functional Loss SNV dbSNP153 33..33 33 - - - 104947 RMVar_ID_104947 Human_SNP_ID_547811025 m1A Human chr14 - 22830250 22830250 22830250 TGGAGTTAACTGCCAGATCAGCGCTTACCCGCATATGACCAGTCTGGGAGCTCGGTAAGGGGCCC TGGAGTTAACTGCCAGATCAGCGCTTACCCGCCTATGACCAGTCTGGGAGCTCGGTAAGGGGCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:22830226..22830250 26863196 MeRIP-seq:(Medium) rs757364045 Functional Loss SNV dbSNP153 33..33 33 - - - 104948 RMVar_ID_104948 Human_SNP_ID_547814426 m1A Human chr14 - 22842625 22842625 22842625 CAATGTTGGGGCCTGGGAAGTAGGCATGGGCCAGGAAGCCGCCCTCACCATCGAAGGGCGTGCTG CAATGTTGGGGCCTGGGAAGTAGGCATGGGCCGGGAAGCCGCCCTCACCATCGAAGGGCGTGCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22842576..22842675 32194978 MeRIP-seq:(Medium) rs1168437251 Functional Loss SNV dbSNP153 33..33 33 - - - 104949 RMVar_ID_104949 Human_SNP_ID_547815839 m1A Human chr14 + 22847124 22847124 22847124 CTTGCTCCTGTTGGTCCCTGTCCTTGCTGCCCAGGCAGCGTGGAGGGGAAGGGTAGGGCAGCCAG CTTGCTCCTGTTGGTCCCTGTCCTTGCTGCCCCGGCAGCGTGGAGGGGAAGGGTAGGGCAGCCAG A C MMP14 Ensembl:ENSG00000157227 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22847076..22847200 32194978 MeRIP-seq:(Medium) rs1417418001 Functional Loss SNV dbSNP153 33..33 33 - - - 104950 RMVar_ID_104950 Human_SNP_ID_547822181 m1A Human chr14 - 22872323 22872317 22872323 TATCGTTTCGGTTCTTACCAAGGAGGAGGAGGAGGAGGGTGGCCAACAGCATCCTGGGCTGTCCA TATCGTTTCGGTTCTTACCAAGGAGGAGGAGG______GTGGCCAACAGCATCCTGGGCTGTCCA CCCTCCT C lnc-RBM23-3 RNACentral:URS0000D57B35 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22871861..22872759 32194978 MeRIP-seq:(Medium) rs745355268 Functional Loss DEL dbSNP153 33..38 33 - - - 104951 RMVar_ID_104951 Human_SNP_ID_547822182 m1A Human chr14 - 22872323 22872317 22872323 TATCGTTTCGGTTCTTACCAAGGAGGAGGAGGAGGAGGGTGGCCAACAGCATCCTGGGCTGTCCA TATCGTTTCGGTTCTTACCAAGGAGGAGGAGG___AGGGTGGCCAACAGCATCCTGGGCTGTCCA CCCTCCT CCCT lnc-RBM23-3 RNACentral:URS0000D57B35 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22871861..22872759 32194978 MeRIP-seq:(Medium) rs745355268 Functional Loss DEL dbSNP153 33..35 33 - - - 104952 RMVar_ID_104952 Human_SNP_ID_547822931 m1A Human chr14 - 22875151 22875151 22875151 GTGATGGTGACGTTGCCCCCGGGCAGCTGCAGAGGGCTGGGAGGTGCCTCACACAGGGAGATCAG GTGATGGTGACGTTGCCCCCGGGCAGCTGCAGCGGGCTGGGAGGTGCCTCACACAGGGAGATCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22875101..22875179 26863196 MeRIP-seq:(Medium) rs765058298 Functional Loss SNV dbSNP153 33..33 33 - - - 104953 RMVar_ID_104953 Human_SNP_ID_547823005 m1A Human chr14 - 22875356 22875356 22875356 CACTGAAACTCTTCCTGCAGGCACATCAGCCAATCTGCAGAGGCACCATGGAGAGGGGCTGTGAA CACTGAAACTCTTCCTGCAGGCACATCAGCCAGTCTGCAGAGGCACCATGGAGAGGGGCTGTGAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22875351..22875400 32194978 MeRIP-seq:(Medium) rs772332284 Functional Loss SNV dbSNP153 33..33 33 - - - 104954 RMVar_ID_104954 Human_SNP_ID_547823128 m1A Human chr14 - 22875649 22875649 22875649 CTCCAAAGCCCAAGTCCAGGGCTGTGAAGCGCACGGCCAGCCGCCGGCCATCATGGGGGTCCAGC CTCCAAAGCCCAAGTCCAGGGCTGTGAAGCGCGCGGCCAGCCGCCGGCCATCATGGGGGTCCAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:22875626..22875650 26863196 MeRIP-seq:(Medium) rs747853225 Functional Loss SNV dbSNP153 33..33 33 - - - 104955 RMVar_ID_104955 Human_SNP_ID_547823263 m1A Human chr14 - 22875972 22875972 22875972 GTCCTCCTCATCTGTGCCGTCAGCACAGTCCCATGAGCCGTCACAGCGCTGTGCCTCACTGTAGC GTCCTCCTCATCTGTGCCGTCAGCACAGTCCCGTGAGCCGTCACAGCGCTGTGCCTCACTGTAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22875921..22876170 32194978 MeRIP-seq:(Medium) rs771794656 Functional Loss SNV dbSNP153 33..33 33 - - - 104956 RMVar_ID_104956 Human_SNP_ID_547823687 m1A Human chr14 + 22877122 22877122 22877122 ACCAACACCCCGGCTCGGGCCTCTGAGGCCAGATCCCAGGTCACACCTTCTGCTGCTCCCCTTGA ACCAACACCCCGGCTCGGGCCTCTGAGGCCAGTTCCCAGGTCACACCTTCTGCTGCTCCCCTTGA A T LRP10 Ensembl:ENSG00000197324 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22877101..22877125 32194978 MeRIP-seq:(Medium) rs762816638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165236,RMVar_hsa_circ_115767,RMVar_hsa_circ_94006,RMVar_hsa_circ_165239 104957 RMVar_ID_104957 Human_SNP_ID_547831763 m1A Human chr14 - 22906370 22906370 22906370 ATGTGGGCATGACTGTAGTTGTTTCCCTCTGTAGTCGTAGTCGAGATCGGGATCGGTATAGACGG ATGTGGGCATGACTGTAGTTGTTTCCCTCTGTTGTCGTAGTCGAGATCGGGATCGGTATAGACGG T A RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22906176..22906410 26863196 MeRIP-seq:(Medium) rs1369496860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_95159,RMVar_hsa_circ_165241,RMVar_hsa_circ_5076,RMVar_hsa_circ_93564,RMVar_hsa_circ_165242,RMVar_hsa_circ_96605,RMVar_hsa_circ_165245,RMVar_hsa_circ_378955,RMVar_hsa_circ_165246,RMVar_hsa_circ_374694,RMVar_hsa_circ_365083,RMVar_hsa_circ_165247,RMVar_hsa_circ_113296,RMVar_hsa_circ_165248,RMVar_hsa_circ_98579,RMVar_hsa_circ_165249,RMVar_hsa_circ_165252,RMVar_hsa_circ_165254,RMVar_hsa_circ_292108,RMVar_hsa_circ_165250,RMVar_hsa_circ_346014,RMVar_hsa_circ_272527,RMVar_hsa_circ_165253,RMVar_hsa_circ_165251 104958 RMVar_ID_104958 Human_SNP_ID_547837059 m1A Human chr14 - 22923094 22923094 22923094 CTTTCTGGCTCCCATCTCTTCCTCCAAGCTGTACAATGAGGTCCGAGCCTGTAGGGAGAAGGACC CTTTCTGGCTCCCATCTCTTCCTCCAAGCTGTGCAATGAGGTCCGAGCCTGTAGGGAGAAGGACC T C PRMT5 Ensembl:ENSG00000100462 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:22922726..22923150 32194978 MeRIP-seq:(Medium) rs1227570701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880798,Human_RBP_ID_8401913,Human_RBP_ID_8793870,Human_RBP_ID_18980146,Human_RBP_ID_22439540,Human_RBP_ID_23616154,Human_RBP_ID_24367376 Human_Splice_Rec_1493784,Human_Splice_Rec_1493785,Human_Splice_Rec_1493820,Human_Splice_Rec_1493821,Human_Splice_Rec_1493852,Human_Splice_Rec_1493853,Human_Splice_Rec_1493882,Human_Splice_Rec_1493883,Human_Splice_Rec_1493892,Human_Splice_Rec_1493893,Human_Splice_Rec_1493901,Human_Splice_Rec_1493930,Human_Splice_Rec_1493931,Human_Splice_Rec_1493960,Human_Splice_Rec_1493961 RMVar_hsa_circ_91236,RMVar_hsa_circ_120979,RMVar_hsa_circ_28883,RMVar_hsa_circ_165259,RMVar_hsa_circ_165260,RMVar_hsa_circ_89103,RMVar_hsa_circ_372379,RMVar_hsa_circ_9143,RMVar_hsa_circ_165261,RMVar_hsa_circ_165262,RMVar_hsa_circ_109845,RMVar_hsa_circ_317381,RMVar_hsa_circ_165263 104959 RMVar_ID_104959 Human_SNP_ID_547837871 m1A Human chr14 + 22926245 22926245 22926245 TGGGGAGAATGGCTGCTTTGATGGGCTCCCCAAGCCAGCGATCAATGACATGATTAGATGGGAGG TGGGGAGAATGGCTGCTTTGATGGGCTCCCCATGCCAGCGATCAATGACATGATTAGATGGGAGG A T PRMT5-AS1 Ensembl:ENSG00000237054 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:22924920..22926354 32194978 MeRIP-seq:(Medium) rs747499939 Functional Loss SNV dbSNP153 33..33 33 - - - 104960 RMVar_ID_104960 Human_SNP_ID_547838535 m1A Human chr14 - 22928617 22928617 22928617 TCTTTACATGATTCTGGGTCTGTCGCGGTTGTAGGTTTGATTTCCTCTGCATGCCTGTCTTCCAT TCTTTACATGATTCTGGGTCTGTCGCGGTTGTGGGTTTGATTTCCTCTGCATGCCTGTCTTCCAT T C PRMT5 Ensembl:ENSG00000100462 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22928576..22928625 26863196 MeRIP-seq:(Medium) rs112214524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4288085,Human_RBP_ID_22648731,Human_RBP_ID_23616165 104961 RMVar_ID_104961 Human_SNP_ID_547846293 m1A Human chr14 - 22956968 22956968 22956968 TGGGGTGTAGACGCTGCTGGCCAGCCCGCCCCAGCCGAGGTTCTCGGCACCGCCTTGAGAGCTTC TGGGGTGTAGACGCTGCTGGCCAGCCCGCCCCCGCCGAGGTTCTCGGCACCGCCTTGAGAGCTTC T G AL132780.3,HAUS4,MIR4707 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036,Ensembl:ENSG00000284118 Protein coding,Protein coding,miRNA intron,5'UTR,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22956926..22956975 32194978 MeRIP-seq:(Medium) rs1158707105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308206,Human_RBP_ID_5176765,Human_RBP_ID_5315622,Human_RBP_ID_5352703,Human_RBP_ID_8182519,Human_RBP_ID_17481279,Human_RBP_ID_18418051,Human_RBP_ID_18926466,Human_RBP_ID_20001332,Human_RBP_ID_22438651,Human_RBP_ID_22532559,Human_RBP_ID_22758743,Human_RBP_ID_24530890 Human_Splice_Rec_1494115,Human_Splice_Rec_1494131,Human_Splice_Rec_1494161,Human_Splice_Rec_1494179,Human_Splice_Rec_1494207,Human_Splice_Rec_1494255,Human_Splice_Rec_1494269,Human_Splice_Rec_1494279,Human_Splice_Rec_1494305,Human_Splice_Rec_1494329 Human_miRNA_ID_3133515,Human_miRNA_ID_3133529,Human_miRNA_ID_3133775,Human_miRNA_ID_3137870,Human_miRNA_ID_3142192,Human_miRNA_ID_3143426 104962 RMVar_ID_104962 Human_SNP_ID_547850115 m1A Human chr14 - 22972186 22972186 22972186 AACTGGAGGGAGCAAAACACTGATTTGATACTAGTCAGTTTGCTTGAAACTAGTTCACCTAAAGC AACTGGAGGGAGCAAAACACTGATTTGATACTGGTCAGTTTGCTTGAAACTAGTTCACCTAAAGC T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430513 Human_miRNA_ID_932392,Human_miRNA_ID_1006039 104963 RMVar_ID_104963 Human_SNP_ID_547850746 m1A Human chr14 - 22974733 22974732 22974733 TGGCCTCCTGCCAGAAGTGGTAGTGCCAAGGAATGTACTCTGTGAAGATTCCCGTGTGACTCTGC TGGCCTCCTGCCAGAAGTGGTAGTGCCAAGGA_TGTACTCTGTGAAGATTCCCGTGTGACTCTGC AT A AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22974731..22974831 32194978 MeRIP-seq:(Medium) rs898240820 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5351961 RMVar_hsa_circ_165279,RMVar_hsa_circ_101496,RMVar_hsa_circ_105346,RMVar_hsa_circ_165280 104964 RMVar_ID_104964 Human_SNP_ID_547850832 m1A Human chr14 + 22975064 22975063 22975064 CATCCAGGCACTTGTTGCAAACAATGCATCGGAAACAGCCTGGATGATAGGACTTCCCCATTGCT CATCCAGGCACTTGTTGCAAACAATGCATCGG_AACAGCCTGGATGATAGGACTTCCCCATTGCT GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:22975013..22975114 32194978 MeRIP-seq:(Medium) rs1422828825 Functional Loss DEL dbSNP153 33..33 33 - - - 104965 RMVar_ID_104965 Human_SNP_ID_547852555 m1A Human chr14 - 22981900 22981900 22981900 AGCCCACGGCCCCGGCCCTCAGCCCCCGCTCTAGCTTCGCCAGTAGCTCGGCCAGCGACGCGAGC AGCCCACGGCCCCGGCCCTCAGCCCCCGCTCTCGCTTCGCCAGTAGCTCGGCCAGCGACGCGAGC T G AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22981776..22981982 26863196 MeRIP-seq:(Medium) rs1347974004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22045162,Human_RBP_ID_27430536 104966 RMVar_ID_104966 Human_SNP_ID_547856752 m1A Human chr14 - 22998637 22998637 22998637 TCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAAAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGC TCCCCACCTGAGGAGCCTGGGCCTCTCAAGGAGAGTCCCGGGGAAGCCTTTAAGGCTCTGTCTGC T C C14orf93 Ensembl:ENSG00000100802 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:22998598..22998799 26863196 MeRIP-seq:(Medium) rs371090817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51747,RMVar_hsa_circ_318883,RMVar_hsa_circ_372260,RMVar_hsa_circ_165284 104967 RMVar_ID_104967 Human_SNP_ID_547863922 m1A Human chr14 + 23026316 23026316 23026316 ATCCATGACCCCATATGCATACACAGAGCCAGAACCTACAGAGAAGGTGGCCCCTGAAATCCGGT ATCCATGACCCCATATGCATACACAGAGCCAGCACCTACAGAGAAGGTGGCCCCTGAAATCCGGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23026201..23026375 32194978 MeRIP-seq:(Medium) rs1285060673 Functional Loss SNV dbSNP153 33..33 33 - - - 104968 RMVar_ID_104968 Human_SNP_ID_547866188 m1A Human chr14 - 23034750 23034750 23034750 AGTCTCAGTGATGGTCTGAGCCTGGCCGCGCCAGGCTGGGGTGTCCCAGAAGAGCCAGGAATCGA AGTCTCAGTGATGGTCTGAGCCTGGCCGCGCCCGGCTGGGGTGTCCCAGAAGAGCCAGGAATCGA T G PSMB5 Ensembl:ENSG00000100804 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23034701..23034750 32194978 MeRIP-seq:(Medium) rs755544933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231060,Human_RBP_ID_443633,Human_RBP_ID_1491584,Human_RBP_ID_4288270,Human_RBP_ID_5315623,Human_RBP_ID_9040147,Human_RBP_ID_9282501,Human_RBP_ID_9323729,Human_RBP_ID_17846505,Human_RBP_ID_18189468,Human_RBP_ID_22438475,Human_RBP_ID_22757831,Human_RBP_ID_22797560,Human_RBP_ID_23208496,Human_RBP_ID_23616272,Human_RBP_ID_27225643 Human_Splice_Rec_1494591,Human_Splice_Rec_1494595,Human_Splice_Rec_1494599,Human_Splice_Rec_1494605 RMVar_hsa_circ_76086,RMVar_hsa_circ_165287 104969 RMVar_ID_104969 Human_SNP_ID_547869789 m1A Human chr14 + 23047921 23047917 23047921 CTGCTGCCGCCCGCCTGGACCCCGTGGGGCTCACTCAGAGGGCCTGTGCCCGCTGCCCCCCCCCC CTGCTGCCGCCCGCCTGGACCCCGTGGGG____CTCAGAGGGCCTGTGCCCGCTGCCCCCCCCCC GCTCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23047871..23047974 26863196 MeRIP-seq:(Medium) rs765758055 Functional Loss DEL dbSNP153 30..33 33 - - - 104970 RMVar_ID_104970 Human_SNP_ID_547869791 m1A Human chr14 + 23047921 23047921 23047921 CTGCTGCCGCCCGCCTGGACCCCGTGGGGCTCACTCAGAGGGCCTGTGCCCGCTGCCCCCCCCCC CTGCTGCCGCCCGCCTGGACCCCGTGGGGCTCTCTCAGAGGGCCTGTGCCCGCTGCCCCCCCCCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23047871..23047974 26863196 MeRIP-seq:(Medium) rs994157537 Functional Loss SNV dbSNP153 33..33 33 - - - 104971 RMVar_ID_104971 Human_SNP_ID_547870111 m1A Human chr14 + 23048387 23048387 23048387 GGTGTCCTCCTCGCCGCCGCCCTCGTCGTCGTAGGTGATGATGTTCTCTCGGACGTCCTCCTCCT GGTGTCCTCCTCGCCGCCGCCCTCGTCGTCGTGGGTGATGATGTTCTCTCGGACGTCCTCCTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23048337..23048418 26863196 MeRIP-seq:(Medium) rs1288098979 Functional Loss SNV dbSNP153 33..33 33 - - - 104972 RMVar_ID_104972 Human_SNP_ID_547871825 m1A Human chr14 - 23054221 23054221 23054221 ACCTGGGGGACAACGCCCTGATGGCATACAGCATCCTGGATGGGGAGGGGTCTGAGGCCTTCAGC ACCTGGGGGACAACGCCCTGATGGCATACAGCGTCCTGGATGGGGAGGGGTCTGAGGCCTTCAGC T C CDH24 Ensembl:ENSG00000139880 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23054172..23054323 32194978 MeRIP-seq:(Medium) rs772647752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1494625,Human_Splice_Rec_1494649,Human_Splice_Rec_1494689,Human_Splice_Rec_1494709 RMVar_hsa_circ_95104,RMVar_hsa_circ_165290 104973 RMVar_ID_104973 Human_SNP_ID_547872802 m1A Human chr14 + 23057475 23057439 23057476 CGCCCGCCCCCGTCGCCGGGTCCCGGGGGCACAGCCCCGAGCCGATTGGAGCGGGCGCCGCGGCT __________________________________CCCCGAGCCGATTGGAGCGGGCGCCGCGGCT CCCCCGCCCGCCCCCGTCGCCGGGTCCCGGGGGCACAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23057424..23057497 26863196 MeRIP-seq:(Medium) rs997146934 Functional Loss DEL dbSNP153 1..34 33 - - - 104974 RMVar_ID_104974 Human_SNP_ID_547873471 m1A Human chr14 - 23059337 23059337 23059337 CGGGAACGGAACCGACAGCTGGAGCGAGAGAAACGTCGGGAGCACAGTCGGGAGAGGGACAGGGA CGGGAACGGAACCGACAGCTGGAGCGAGAGAAGCGTCGGGAGCACAGTCGGGAGAGGGACAGGGA T C ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23058844..23061525 26863196 MeRIP-seq:(Medium) rs1227728461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40708,Human_RBP_ID_5177001,Human_RBP_ID_5522605,Human_RBP_ID_5563077,Human_RBP_ID_6333978,Human_RBP_ID_8230388,Human_RBP_ID_12300119,Human_RBP_ID_22044444,Human_RBP_ID_22926208,Human_RBP_ID_23113651,Human_RBP_ID_23118217,Human_RBP_ID_23616376,Human_RBP_ID_24543642,Human_RBP_ID_26324882,Human_RBP_ID_26922654 104975 RMVar_ID_104975 Human_SNP_ID_547873477 m1A Human chr14 - 23059360 23059360 23059360 AGGAGCGGGAGAAGGAAGCCGAGCGGGAACGGAACCGACAGCTGGAGCGAGAGAAACGTCGGGAG AGGAGCGGGAGAAGGAAGCCGAGCGGGAACGGCACCGACAGCTGGAGCGAGAGAAACGTCGGGAG T G ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:23059166..23059401 26863196 MeRIP-seq:(Medium) rs1252691462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4401,Human_RBP_ID_40708,Human_RBP_ID_196983,Human_RBP_ID_881520,Human_RBP_ID_3944816,Human_RBP_ID_4288364,Human_RBP_ID_5112648,Human_RBP_ID_5176011,Human_RBP_ID_5522605,Human_RBP_ID_8182037,Human_RBP_ID_8230388,Human_RBP_ID_18161210,Human_RBP_ID_18411071,Human_RBP_ID_22044742,Human_RBP_ID_22926208,Human_RBP_ID_23113651,Human_RBP_ID_23118217,Human_RBP_ID_24543642,Human_RBP_ID_25089592,Human_RBP_ID_26324882,Human_RBP_ID_27808691 104976 RMVar_ID_104976 Human_SNP_ID_547873481 m1A Human chr14 - 23059364 23059364 23059364 CAAAAGGAGCGGGAGAAGGAAGCCGAGCGGGAACGGAACCGACAGCTGGAGCGAGAGAAACGTCG CAAAAGGAGCGGGAGAAGGAAGCCGAGCGGGAGCGGAACCGACAGCTGGAGCGAGAGAAACGTCG T C ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23059051..23061489 26863196 MeRIP-seq:(Medium) rs920178613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4401,Human_RBP_ID_40708,Human_RBP_ID_196983,Human_RBP_ID_881520,Human_RBP_ID_3944816,Human_RBP_ID_4288365,Human_RBP_ID_5112648,Human_RBP_ID_5176011,Human_RBP_ID_5522605,Human_RBP_ID_8182037,Human_RBP_ID_8230388,Human_RBP_ID_18161210,Human_RBP_ID_18411071,Human_RBP_ID_22044742,Human_RBP_ID_22926208,Human_RBP_ID_23113651,Human_RBP_ID_23118217,Human_RBP_ID_24543642,Human_RBP_ID_25089592,Human_RBP_ID_26324882,Human_RBP_ID_27808691 104977 RMVar_ID_104977 Human_SNP_ID_547874146 m1A Human chr14 + 23061371 23061371 23061371 TTGCGGCGGCGGTCACGGGACCTTGATCGGGAACGGGGCCCTTCTCGAACTTTGTCCCGATCCCA TTGCGGCGGCGGTCACGGGACCTTGATCGGGAGCGGGGCCCTTCTCGAACTTTGTCCCGATCCCA A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:23061207..23061502 26863196 MeRIP-seq:(Medium) rs149108570 Functional Loss SNV dbSNP153 33..33 33 - - - 104978 RMVar_ID_104978 Human_SNP_ID_547875071 m1A Human chr14 - 23064142 23064142 23064142 TGAGACAGAGCGTAATGGCGATGATGGGACCCATGACAAGGGGCTGAAAATATGCCGGACAGTCA TGAGACAGAGCGTAATGGCGATGATGGGACCCGTGACAAGGGGCTGAAAATATGCCGGACAGTCA T C ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23063567..23064443 32194978 MeRIP-seq:(Medium) rs1258842639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_39399,Human_RBP_ID_443676,Human_RBP_ID_1491629,Human_RBP_ID_1816885,Human_RBP_ID_3944826,Human_RBP_ID_4288418,Human_RBP_ID_5522614,Human_RBP_ID_6334014,Human_RBP_ID_8793926,Human_RBP_ID_9368447,Human_RBP_ID_12300161,Human_RBP_ID_18980176,Human_RBP_ID_22495304,Human_RBP_ID_23256191,Human_RBP_ID_26326198 Human_Splice_Rec_1494731,Human_Splice_Rec_1494752,Human_Splice_Rec_1494753,Human_Splice_Rec_1494775,Human_Splice_Rec_1494799,Human_Splice_Rec_1494835,Human_Splice_Rec_1494871,Human_Splice_Rec_1494905,Human_Splice_Rec_1494927,Human_Splice_Rec_1494962,Human_Splice_Rec_1494963,Human_Splice_Rec_1494978,Human_Splice_Rec_1494979,Human_Splice_Rec_1494995,Human_Splice_Rec_1495003,Human_Splice_Rec_1495005,Human_Splice_Rec_1495016,Human_Splice_Rec_1495017,Human_Splice_Rec_1495022,Human_Splice_Rec_1495023,Human_Splice_Rec_1495029 RMVar_hsa_circ_15690,RMVar_hsa_circ_165292,RMVar_hsa_circ_284669,RMVar_hsa_circ_320084,RMVar_hsa_circ_63406,RMVar_hsa_circ_109025,RMVar_hsa_circ_165293,RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_35680 104979 RMVar_ID_104979 Human_SNP_ID_547876432 m1A Human chr14 + 23069417 23069417 23069417 CCACCGTGTAAGAGGGATCACTAGAGTGCTCTACTCTTTCCCCTAGGTCCATTCCTGCCCACCCG CCACCGTGTAAGAGGGATCACTAGAGTGCTCTCCTCTTTCCCCTAGGTCCATTCCTGCCCACCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23069415..23069540 26863196 MeRIP-seq:(Medium) rs557608775 Functional Loss SNV dbSNP153 33..33 33 - - - 104980 RMVar_ID_104980 Human_SNP_ID_547877170 m1A Human chr14 + 23071518 23071518 23071518 GCTGGTAGTGGCTGGCTCTATTGTATTGGCGGAGCGGCAGCGATCAGCCGGAGACATGCAGGGGA GCTGGTAGTGGCTGGCTCTATTGTATTGGCGGGGCGGCAGCGATCAGCCGGAGACATGCAGGGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:23071323..23071575;chr14:23071425..23071534;chr14:23071439..23071575 26863196 MeRIP-seq:(Medium) rs1221720424 Functional Loss SNV dbSNP153 33..33 33 - - - 104981 RMVar_ID_104981 Human_SNP_ID_547879329 m1A Human chr14 - 23079719 23079719 23079719 CTCCAGTTCTAGATCAAGATCTCGCTCTCCTGACAGTTCAGGTTCTCGGTCTCATTCACCGCTCA CTCCAGTTCTAGATCAAGATCTCGCTCTCCTGGCAGTTCAGGTTCTCGGTCTCATTCACCGCTCA T C ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23079668..23079833 26863196 MeRIP-seq:(Medium) rs747762869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1491728,Human_RBP_ID_12300822,Human_RBP_ID_17248459 Human_miRNA_ID_2928018 RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_57929,RMVar_hsa_circ_1989,RMVar_hsa_circ_377234,RMVar_hsa_circ_99923,RMVar_hsa_circ_324109,RMVar_hsa_circ_340960,RMVar_hsa_circ_51126,RMVar_hsa_circ_165299,RMVar_hsa_circ_165300,RMVar_hsa_circ_115775,RMVar_hsa_circ_165301 104982 RMVar_ID_104982 Human_SNP_ID_547882214 m1A Human chr14 + 23090037 23090037 23090037 AGCTCTGGTCTCTCCAGGCTGCTCTGAAAGTCAGGAGGCAGCAGGGAAGCCACTCCCTCAGGATG AGCTCTGGTCTCTCCAGGCTGCTCTGAAAGTCGGGAGGCAGCAGGGAAGCCACTCCCTCAGGATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23090022..23090592 32194978 MeRIP-seq:(Medium) rs1228782397 Functional Loss SNV dbSNP153 33..33 33 - - - 104983 RMVar_ID_104983 Human_SNP_ID_547883617 m1A Human chr14 - 23095091 23095091 23095091 CCTCACGCAAGATGGCGGAGCTGGAGGAGGTGACTCTGGACGGGAAGCCTCTTCAGGCGCTGCGG CCTCACGCAAGATGGCGGAGCTGGAGGAGGTGTCTCTGGACGGGAAGCCTCTTCAGGCGCTGCGG T A ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:23094963..23095137 26863196 MeRIP-seq:(Medium) rs144430369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813898,Human_RBP_ID_1491740,Human_RBP_ID_4308209,Human_RBP_ID_5563093,Human_RBP_ID_6334340,Human_RBP_ID_8793949,Human_RBP_ID_9282148,Human_RBP_ID_22926211,Human_RBP_ID_23118268 Human_miRNA_ID_1967325,Human_miRNA_ID_2016393,Human_miRNA_ID_2825396,Human_miRNA_ID_2859367 RMVar_hsa_circ_165294,RMVar_hsa_circ_80287 104984 RMVar_ID_104984 Human_SNP_ID_547883711 m1A Human chr14 + 23095233 23095233 23095233 CGCCCACTGCCATACTCTACCCCTCGATTACCACTCAGAACTCCCCGGGTTCCTCCGGATGTCCT CGCCCACTGCCATACTCTACCCCTCGATTACCCCTCAGAACTCCCCGGGTTCCTCCGGATGTCCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23095198..23095368 26863196 MeRIP-seq:(Medium) rs760167213 Functional Loss SNV dbSNP153 33..33 33 - - - 104985 RMVar_ID_104985 Human_SNP_ID_547883712 m1A Human chr14 + 23095233 23095233 23095233 CGCCCACTGCCATACTCTACCCCTCGATTACCACTCAGAACTCCCCGGGTTCCTCCGGATGTCCT CGCCCACTGCCATACTCTACCCCTCGATTACCGCTCAGAACTCCCCGGGTTCCTCCGGATGTCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23095198..23095368 26863196 MeRIP-seq:(Medium) rs760167213 Functional Loss SNV dbSNP153 33..33 33 - - - 104986 RMVar_ID_104986 Human_SNP_ID_547884661 m1A Human chr14 + 23097993 23097993 23097993 GTGGTTTCGAGGCTGGGCTGAGCAGGAGCGCAATGAATTTGTCAGACAGCTGGAGTTCAGTGAGC GTGGTTTCGAGGCTGGGCTGAGCAGGAGCGCAGTGAATTTGTCAGACAGCTGGAGTTCAGTGAGC A G C14orf119 Ensembl:ENSG00000179933 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23097944..23098128 26863196 MeRIP-seq:(Medium) rs1464777026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443694,Human_RBP_ID_757382,Human_RBP_ID_814022,Human_RBP_ID_1491748,Human_RBP_ID_5112649,Human_RBP_ID_5140728,Human_RBP_ID_17651311,Human_RBP_ID_22044754,Human_RBP_ID_22439074,Human_RBP_ID_22757832,Human_RBP_ID_23616488,Human_RBP_ID_27225700 RMVar_hsa_circ_124089,RMVar_hsa_circ_165303 104987 RMVar_ID_104987 Human_SNP_ID_547929462 m1A Human chr14 + 23275536 23275536 23275536 TTTCTTTGTTTAAACAGTTACTAAGTTGGTTCATCTTTCAGTAACAGACCTCCCCTCCCCCAGCT TTTCTTTGTTTAAACAGTTACTAAGTTGGTTCGTCTTTCAGTAACAGACCTCCCCTCCCCCAGCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23275533..23275697 26863196 MeRIP-seq:(Medium) rs1373686336 Functional Loss SNV dbSNP153 33..33 33 - - - 104988 RMVar_ID_104988 Human_SNP_ID_547929465 m1A Human chr14 + 23275543 23275543 23275543 GTTTAAACAGTTACTAAGTTGGTTCATCTTTCAGTAACAGACCTCCCCTCCCCCAGCTCCCCACT GTTTAAACAGTTACTAAGTTGGTTCATCTTTCGGTAACAGACCTCCCCTCCCCCAGCTCCCCACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23275493..23275881 26863196 MeRIP-seq:(Medium) rs938166110 Functional Loss SNV dbSNP153 33..33 33 - - - 104989 RMVar_ID_104989 Human_SNP_ID_547929788 m1A Human chr14 - 23276289 23276289 23276289 TCTAAACCCCTCCAGCCACTAGGCTGTGTCCCACAGTCAGTGTCACCCAGTGAACAGGCATTACC TCTAAACCCCTCCAGCCACTAGGCTGTGTCCCTCAGTCAGTGTCACCCAGTGAACAGGCATTACC T A HOMEZ Ensembl:ENSG00000215271 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:23276178..23276318 26863196 MeRIP-seq:(Medium) rs1434391167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1495428 104990 RMVar_ID_104990 Human_SNP_ID_547930127 m1A Human chr14 + 23277182 23277182 23277182 AGGCATGGTGCCTTCTGATTTGTGCCCTTCAGAGATAGCTGCAATAAGAAGACAAACAGCTCAAT AGGCATGGTGCCTTCTGATTTGTGCCCTTCAGGGATAGCTGCAATAAGAAGACAAACAGCTCAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:23276907..23285323 32194978 MeRIP-seq:(Medium) rs1318556757 Functional Loss SNV dbSNP153 33..33 33 - - - 104991 RMVar_ID_104991 Human_SNP_ID_547932941 m1A Human chr14 + 23285892 23285892 23285892 GGAGACCGTACACGAGCTGGGAGGGGAAGTCCAAGGGGCTGGGGATCACTCACCGCAGTCCAGCC GGAGACCGTACACGAGCTGGGAGGGGAAGTCCCAGGGGCTGGGGATCACTCACCGCAGTCCAGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23285888..23286050 26863196 MeRIP-seq:(Medium) rs1381772635 Functional Loss SNV dbSNP153 33..33 33 - - - 104992 RMVar_ID_104992 Human_SNP_ID_547936865 m1A Human chr14 - 23301121 23301121 23301121 AACGGCACCGGAGGGATTATAAAAAAAGGAAAAGAATGGGGATGATGGTGGCCTTCCCTTCAGTG AACGGCACCGGAGGGATTATAAAAAAAGGAAACGAATGGGGATGATGGTGGCCTTCCCTTCAGTG T G PPP1R3E Ensembl:ENSG00000235194 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23300795..23302856 26863196 MeRIP-seq:(Medium) rs1370747697 Functional Loss SNV dbSNP153 33..33 33 - - - 104993 RMVar_ID_104993 Human_SNP_ID_547936997 m1A Human chr14 + 23301478 23301478 23301478 TGGATCCAGCCCTGCGGCTCCGGAGCTCCGCCACTGCCCGGGTGCTCGGGCCCACGTAGAGCATA TGGATCCAGCCCTGCGGCTCCGGAGCTCCGCCGCTGCCCGGGTGCTCGGGCCCACGTAGAGCATA A G BCL2L2 Ensembl:ENSG00000129473 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23300859..23301731 26863196 MeRIP-seq:(Medium) rs888069969 Functional Loss SNV dbSNP153 33..33 33 - - - 104994 RMVar_ID_104994 Human_SNP_ID_547938574 m1A Human chr14 - 23306889 23306889 23306889 GCCCGCCTGCCAGGTTAGGGATCTCACGGGTCAGGCCGCTGCCGGGATCCGGGCCGTTTCCTGGT GCCCGCCTGCCAGGTTAGGGATCTCACGGGTCGGGCCGCTGCCGGGATCCGGGCCGTTTCCTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23306880..23306975 26863196 MeRIP-seq:(Medium) rs1479383154 Functional Loss SNV dbSNP153 33..33 33 - - - 104995 RMVar_ID_104995 Human_SNP_ID_547939146 m1A Human chr14 + 23309089 23309089 23309089 GATGGGTGGGCATGGAACAGGATGGGCAGAGAAAGGGTAGTGTGTGAGGGAGCTGAGTAGGCCAG GATGGGTGGGCATGGAACAGGATGGGCAGAGAGAGGGTAGTGTGTGAGGGAGCTGAGTAGGCCAG A G BCL2L2,BCL2L2-PABPN1 Ensembl:ENSG00000129473,Ensembl:ENSG00000258643 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23308816..23309294 26863196 MeRIP-seq:(Medium) rs1281787291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813561,Human_RBP_ID_5140837,Human_RBP_ID_6334607,Human_RBP_ID_9417725,Human_RBP_ID_18936626,Human_RBP_ID_23616579,Human_RBP_ID_26431594,Human_RBP_ID_26778284 Human_miRNA_ID_2450646,Human_miRNA_ID_2540091 RMVar_hsa_circ_165309,RMVar_hsa_circ_378376,RMVar_hsa_circ_165310 104996 RMVar_ID_104996 Human_SNP_ID_547939524 m1A Human chr14 - 23310822 23310822 23310822 TAAGACAGCTACAAGGGGAGCTGTTCTGTTTGAGGGCAAATTGCCCAGCCTGCTCAGCTCCCCAC TAAGACAGCTACAAGGGGAGCTGTTCTGTTTGGGGGCAAATTGCCCAGCCTGCTCAGCTCCCCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23310711..23310911 32194978 MeRIP-seq:(Medium) rs183445900 Functional Loss SNV dbSNP153 33..33 33 - - - 104997 RMVar_ID_104997 Human_SNP_ID_547941966 m1A Human chr14 + 23321496 23321496 23321496 GCGGCGATGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGGGGCTGCGGGCGGTCGGGGCTCCGG GCGGCGATGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGGGCTGCGGGCGGTCGGGGCTCCGG A G PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding CDS,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:23321451..23321894 26863196 MeRIP-seq:(Medium) rs1310993566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231628,Human_RBP_ID_443817,Human_RBP_ID_4289370,Human_RBP_ID_5176021,Human_RBP_ID_8725679,Human_RBP_ID_9323733,Human_RBP_ID_9417874,Human_RBP_ID_17067554,Human_RBP_ID_18418060,Human_RBP_ID_26778286 104998 RMVar_ID_104998 Human_SNP_ID_547941967 m1A Human chr14 + 23321496 23321496 23321496 GCGGCGATGGCGGCGGCGGCGGCGGCGGCAGCAGCAGCGGGGGCTGCGGGCGGTCGGGGCTCCGG GCGGCGATGGCGGCGGCGGCGGCGGCGGCAGCTGCAGCGGGGGCTGCGGGCGGTCGGGGCTCCGG A T PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding CDS,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:23321451..23321894 26863196 MeRIP-seq:(Medium) rs1310993566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231628,Human_RBP_ID_443817,Human_RBP_ID_4289370,Human_RBP_ID_5176021,Human_RBP_ID_8725679,Human_RBP_ID_9323733,Human_RBP_ID_9417874,Human_RBP_ID_17067554,Human_RBP_ID_18418060,Human_RBP_ID_26778286 104999 RMVar_ID_104999 Human_SNP_ID_547942006 m1A Human chr14 + 23321570 23321570 23321570 GCGGCGCCATCTTGTGCCCGGGGCCGGTGGGGAGGCCGGGGAGGGGGCCCCGGGGGGCGCAGGGG GCGGCGCCATCTTGTGCCCGGGGCCGGTGGGGGGGCCGGGGAGGGGGCCCCGGGGGGCGCAGGGG A G PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding CDS,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:23321476..23321686 26863410 MeRIP-seq:(Medium) rs1300739575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944834,Human_RBP_ID_4311644,Human_RBP_ID_5112804,Human_RBP_ID_5140737,Human_RBP_ID_5176022,Human_RBP_ID_5351998,Human_RBP_ID_6334744,Human_RBP_ID_9323735,Human_RBP_ID_9352941,Human_RBP_ID_9417728,Human_RBP_ID_9761096,Human_RBP_ID_18417905,Human_RBP_ID_27225758,Human_RBP_ID_27837218 105000 RMVar_ID_105000 Human_SNP_ID_547942275 m1A Human chr14 - 23322135 23322135 23322135 GGAGGGTATGGAGGACAGCTTAAGAGGAACCAACGCAGGGGCTGTGCCCTGCTCTCGGCCAGAGC GGAGGGTATGGAGGACAGCTTAAGAGGAACCAGCGCAGGGGCTGTGCCCTGCTCTCGGCCAGAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23322133..23323447 32194978 MeRIP-seq:(Medium) rs1177115660 Functional Loss SNV dbSNP153 33..33 33 - - - 105001 RMVar_ID_105001 Human_SNP_ID_547942309 m1A Human chr14 + 23322179 23322179 23322179 AAGCTGTCCTCCATACCCTCCCCACTTATATTAGGAGCTGGAAGCTATCAAAGCTCGAGTCAGGG AAGCTGTCCTCCATACCCTCCCCACTTATATTGGGAGCTGGAAGCTATCAAAGCTCGAGTCAGGG A G PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:23322176..23322275 26863196 MeRIP-seq:(Medium) rs929314618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1491818,Human_RBP_ID_5177007,Human_RBP_ID_8076266,Human_RBP_ID_22577036,Human_RBP_ID_27430652 RMVar_hsa_circ_72986,RMVar_hsa_circ_357797,RMVar_hsa_circ_56732 105002 RMVar_ID_105002 Human_SNP_ID_547942876 m1A Human chr14 + 23324194 23324194 23324194 CCAGGCATCAGCACAACAGACCGGGGTTTTCCACGAGCCCGCTACCGCGCCCGGACCACCAACTA CCAGGCATCAGCACAACAGACCGGGGTTTTCCGCGAGCCCGCTACCGCGCCCGGACCACCAACTA A G PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:23324024..23325753;chr14:23323951..23325800;chr14:23323976..23325534 26863196 MeRIP-seq:(Medium) rs545069653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231096,Human_RBP_ID_443831,Human_RBP_ID_813635,Human_RBP_ID_1361145,Human_RBP_ID_1491831,Human_RBP_ID_6334770,Human_RBP_ID_8402111,Human_RBP_ID_9369751,Human_RBP_ID_12301956,Human_RBP_ID_17246942,Human_RBP_ID_17846637,Human_RBP_ID_22044470,Human_RBP_ID_23616639,Human_RBP_ID_26922948 Human_Splice_Rec_1495520,Human_Splice_Rec_1495521,Human_Splice_Rec_1495540,Human_Splice_Rec_1495541,Human_Splice_Rec_1495552,Human_Splice_Rec_1495553,Human_Splice_Rec_1495564,Human_Splice_Rec_1495572,Human_Splice_Rec_1495573,Human_Splice_Rec_1495584,Human_Splice_Rec_1495592,Human_Splice_Rec_1495596,Human_Splice_Rec_1495600 RMVar_hsa_circ_12530,RMVar_hsa_circ_72986,RMVar_hsa_circ_165313,RMVar_hsa_circ_282196 105003 RMVar_ID_105003 Human_SNP_ID_547942929 m1A Human chr14 - 23324283 23324283 23324283 AAGAGGAGCAGCCCATCTATCCTGACCTGTAGACGCGACCCCGGGGCCTGCTGTTAAAACCACTG AAGAGGAGCAGCCCATCTATCCTGACCTGTAGGCGCGACCCCGGGGCCTGCTGTTAAAACCACTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:23323484..23325325 32194978 MeRIP-seq:(Medium) rs762744505 Functional Loss SNV dbSNP153 33..33 33 - - - 105004 RMVar_ID_105004 Human_SNP_ID_547943490 m1A Human chr14 - 23325943 23325943 23325943 AAAACAAAAACACCCCTAAACCCCCCAAAACAAGGTAGTGCATTTCCCCAGGGGGAAGGGGAATT AAAACAAAAACACCCCTAAACCCCCCAAAACACGGTAGTGCATTTCCCCAGGGGGAAGGGGAATT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23325893..23326061 26863196 MeRIP-seq:(Medium) rs926828792 Functional Loss SNV dbSNP153 33..33 33 - - - 105005 RMVar_ID_105005 Human_SNP_ID_547943509 m1A Human chr14 - 23325997 23325987 23325997 AAAGGGAAAAAAGGCAAAGGAAAAAAAAAAAAAACAAAAAAACAAAACAACTGAAAAACAAAAAC AAAGGGAAAAAAGGCAAAGGAAAAAAAAAAAA__________CAAAACAACTGAAAAACAAAAAC GTTTTTTTGTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23325959..23326056 26863196 MeRIP-seq:(Medium) rs992485914 Functional Loss DEL dbSNP153 33..42 33 - - - 105006 RMVar_ID_105006 Human_SNP_ID_547948711 m1A Human chr14 + 23346754 23346745 23346754 AAGGCCGGCGACACAGCTCCCCGTCCCGGAGCACCTCGGGCAGGAGCTTGCGCTTGGTCTCCGGC AAGGCCGGCGACACAGCTCCCCGT_________CCTCGGGCAGGAGCTTGCGCTTGGTCTCCGGC TCCCGGAGCA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23346703..23347612 32194978 MeRIP-seq:(Medium) rs971875799 Functional Loss DEL dbSNP153 25..33 33 - - - 105007 RMVar_ID_105007 Human_SNP_ID_547948718 m1A Human chr14 + 23346754 23346754 23346754 AAGGCCGGCGACACAGCTCCCCGTCCCGGAGCACCTCGGGCAGGAGCTTGCGCTTGGTCTCCGGC AAGGCCGGCGACACAGCTCCCCGTCCCGGAGCGCCTCGGGCAGGAGCTTGCGCTTGGTCTCCGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:23346703..23347612 32194978 MeRIP-seq:(Medium) rs778033498 Functional Loss SNV dbSNP153 33..33 33 - - - 105008 RMVar_ID_105008 Human_SNP_ID_547984485 m1A Human chr14 - 23469729 23469729 23469729 TAGCTACGCGAGGAAGAAACCACACCAAACTCACCAGCGCCGCCATCTTCGCAAAGCCCACCCCT TAGCTACGCGAGGAAGAAACCACACCAAACTCCCCAGCGCCGCCATCTTCGCAAAGCCCACCCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:23469709..23469790;chr14:23469717..23469788;chr14:23469720..23469806 26863196 MeRIP-seq:(Medium) rs1242899736 Functional Loss SNV dbSNP153 33..33 33 - - - 105009 RMVar_ID_105009 Human_SNP_ID_547984641 m1A Human chr14 + 23470094 23470094 23470094 GCCAAGTGCCGTGACACTTCTGAAAAATCTCCAGGAGCAAGTGAGTAGTGTCGCCTCTGGAATAA GCCAAGTGCCGTGACACTTCTGAAAAATCTCCGGGAGCAAGTGAGTAGTGTCGCCTCTGGAATAA A G NGDN Ensembl:ENSG00000129460 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr14:23470026..23470125 26863196 MeRIP-seq:(Medium) rs748887521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880483,Human_RBP_ID_998059,Human_RBP_ID_4308219,Human_RBP_ID_5351629,Human_RBP_ID_9368481,Human_RBP_ID_18980214,Human_RBP_ID_26325680 Human_Splice_Rec_1495992,Human_Splice_Rec_1495993,Human_Splice_Rec_1495996,Human_Splice_Rec_1495998,Human_Splice_Rec_1495999,Human_Splice_Rec_1496008,Human_Splice_Rec_1496009,Human_Splice_Rec_1496028,Human_Splice_Rec_1496029,Human_Splice_Rec_1496046,Human_Splice_Rec_1496047,Human_Splice_Rec_1496057,Human_Splice_Rec_1496067,Human_Splice_Rec_1496069 105010 RMVar_ID_105010 Human_SNP_ID_547986050 m1A Human chr14 + 23475223 23475223 23475223 GAAAGACCAGCTGCTGCTCATGTACCTTATGGATTTGACCCACCTCATTCTGGACAAAGCCTCAG GAAAGACCAGCTGCTGCTCATGTACCTTATGGGTTTGACCCACCTCATTCTGGACAAAGCCTCAG A G NGDN Ensembl:ENSG00000129460 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23475124..23475250 26863196 MeRIP-seq:(Medium) rs575716360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443874,Human_RBP_ID_1491873,Human_RBP_ID_1817047,Human_RBP_ID_9368485,Human_RBP_ID_18648376,Human_RBP_ID_26324923 Human_Splice_Rec_1496002,Human_Splice_Rec_1496012,Human_Splice_Rec_1496013,Human_Splice_Rec_1496032,Human_Splice_Rec_1496033,Human_Splice_Rec_1496050,Human_Splice_Rec_1496060,Human_Splice_Rec_1496061,Human_Splice_Rec_1496072,Human_Splice_Rec_1496073 RMVar_hsa_circ_31676 105011 RMVar_ID_105011 Human_SNP_ID_547986449 m1A Human chr14 + 23476326 23476326 23476326 ATTGAGCAGCTCTGTCATTCGTGAACTTAAGGAGCAGTACTCAGATGCTCCAGAGGAAATCCGTG ATTGAGCAGCTCTGTCATTCGTGAACTTAAGGGGCAGTACTCAGATGCTCCAGAGGAAATCCGTG A G NGDN Ensembl:ENSG00000129460 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:23476276..23476400 32194978 MeRIP-seq:(Medium) rs759212285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1491882,Human_RBP_ID_9368491,Human_RBP_ID_23616696,Human_RBP_ID_26324924,Human_RBP_ID_26807977 Human_Splice_Rec_1496020,Human_Splice_Rec_1496021,Human_Splice_Rec_1496040,Human_Splice_Rec_1496041,Human_Splice_Rec_1496052,Human_Splice_Rec_1496053,Human_Splice_Rec_1496076,Human_Splice_Rec_1496077,Human_Splice_Rec_1496088,Human_Splice_Rec_1496089,Human_Splice_Rec_1496093,Human_Splice_Rec_1496099 Human_miRNA_ID_1993685,Human_miRNA_ID_2404156 RMVar_hsa_circ_165317,RMVar_hsa_circ_375498,RMVar_hsa_circ_374186,RMVar_hsa_circ_266515,RMVar_hsa_circ_165318 105012 RMVar_ID_105012 Human_SNP_ID_548003883 m1A Human chr14 - 23544916 23544916 23544916 GGGGTGCAGAAAAACGGCCAGGGAAAAGAACAATGGGGGACAGGAAAGGGAAACCTGGTAGGAGG GGGGTGCAGAAAAACGGCCAGGGAAAAGAACAGTGGGGGACAGGAAAGGGAAACCTGGTAGGAGG T C ZFHX2 Ensembl:ENSG00000136367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23544914..23544979 26863196 MeRIP-seq:(Medium) rs1021428845 Functional Loss SNV dbSNP153 33..33 33 - - - 105013 RMVar_ID_105013 Human_SNP_ID_548004516 m1A Human chr14 - 23548168 23548168 23548168 GACGGAAGAGGAGGACTAGAAATGGCAGTTACAGAATGTGAAAGGAGAAGGGCTTTGTGAGTGGG GACGGAAGAGGAGGACTAGAAATGGCAGTTACGGAATGTGAAAGGAGAAGGGCTTTGTGAGTGGG T C ZFHX2 Ensembl:ENSG00000136367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23548150..23548215 26863196 MeRIP-seq:(Medium) rs1318169388 Functional Loss SNV dbSNP153 33..33 33 - - - 105014 RMVar_ID_105014 Human_SNP_ID_548005227 m1A Human chr14 - 23551160 23551156 23551160 CTGGGGGAGGGGACAAGGACGGACGGACAGACAGACCGAGAGCCCTGGGAGATAGCAGACAGGGG CTGGGGGAGGGGACAAGGACGGACGGACAGAC____CGAGAGCCCTGGGAGATAGCAGACAGGGG GGTCT G ZFHX2 Ensembl:ENSG00000136367 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551118..23551205 26863196 MeRIP-seq:(Medium) rs1183662640 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8180863 105015 RMVar_ID_105015 Human_SNP_ID_548005230 m1A Human chr14 - 23551160 23551160 23551160 CTGGGGGAGGGGACAAGGACGGACGGACAGACAGACCGAGAGCCCTGGGAGATAGCAGACAGGGG CTGGGGGAGGGGACAAGGACGGACGGACAGACGGACCGAGAGCCCTGGGAGATAGCAGACAGGGG T C ZFHX2 Ensembl:ENSG00000136367 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551118..23551205 26863196 MeRIP-seq:(Medium) rs111842708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8180863 105016 RMVar_ID_105016 Human_SNP_ID_548005342 m1A Human chr14 - 23551664 23551652 23551664 GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGGAGGAGGAGGAGGCAGGGAGCGAGCGAGTGCCCA GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGG____________CAGGGAGCGAGCGAGTGCCCA GCCTCCTCCTCCT G ZFHX2 Ensembl:ENSG00000136367 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551620..23551755 26863196 MeRIP-seq:(Medium) rs891960070 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_3468631 105017 RMVar_ID_105017 Human_SNP_ID_548005343 m1A Human chr14 - 23551664 23551652 23551664 GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGGAGGAGGAGGAGGCAGGGAGCGAGCGAGTGCCCA GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGG_________AGGCAGGGAGCGAGCGAGTGCCCA GCCTCCTCCTCCT GCCT ZFHX2 Ensembl:ENSG00000136367 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551620..23551755 26863196 MeRIP-seq:(Medium) rs891960070 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_3468631 105018 RMVar_ID_105018 Human_SNP_ID_548005344 m1A Human chr14 - 23551664 23551652 23551664 GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGGAGGAGGAGGAGGCAGGGAGCGAGCGAGTGCCCA GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGG______AGGAGGCAGGGAGCGAGCGAGTGCCCA GCCTCCTCCTCCT GCCTCCT ZFHX2 Ensembl:ENSG00000136367 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551620..23551755 26863196 MeRIP-seq:(Medium) rs891960070 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_3468631 105019 RMVar_ID_105019 Human_SNP_ID_548005345 m1A Human chr14 - 23551664 23551652 23551664 GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGGAGGAGGAGGAGGCAGGGAGCGAGCGAGTGCCCA GGAGGAGGAGGGCGAGGAGGAGAAGGAGGAGG___AGGAGGAGGCAGGGAGCGAGCGAGTGCCCA GCCTCCTCCTCCT GCCTCCTCCT ZFHX2 Ensembl:ENSG00000136367 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23551620..23551755 26863196 MeRIP-seq:(Medium) rs891960070 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3468631 105020 RMVar_ID_105020 Human_SNP_ID_548007408 m1A Human chr14 - 23558949 23558949 23558949 TTAGAGGAGGGGGAAGAAACAGGCAGCGCTGGAGAGAGAGGAGTCACTGTCAGAAGGGACACTGA TTAGAGGAGGGGGAAGAAACAGGCAGCGCTGGGGAGAGAGGAGTCACTGTCAGAAGGGACACTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23558899..23559132 26863196 MeRIP-seq:(Medium) rs368349129 Functional Loss SNV dbSNP153 33..33 33 - - - 105021 RMVar_ID_105021 Human_SNP_ID_548009802 m1A Human chr14 - 23566086 23566086 23566086 CTCTCCAGTGTCTTCCTCCCACCCTGTGCCCAACTGCTTCATGAGCGTCACCATGGTAAGGCTGT CTCTCCAGTGTCTTCCTCCCACCCTGTGCCCACCTGCTTCATGAGCGTCACCATGGTAAGGCTGT T G AP1G2 Ensembl:ENSG00000213983 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:23566051..23566100 32194978 MeRIP-seq:(Medium) rs765851028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757570,Human_RBP_ID_883526,Human_RBP_ID_3944448,Human_RBP_ID_9369796,Human_RBP_ID_18979287 Human_Splice_Rec_1496186,Human_Splice_Rec_1496187,Human_Splice_Rec_1496230,Human_Splice_Rec_1496231,Human_Splice_Rec_1496282,Human_Splice_Rec_1496320,Human_Splice_Rec_1496356,Human_Splice_Rec_1496357,Human_Splice_Rec_1496474,Human_Splice_Rec_1496475,Human_Splice_Rec_1496488,Human_Splice_Rec_1496496,Human_Splice_Rec_1496504,Human_Splice_Rec_1496505,Human_Splice_Rec_1496516,Human_Splice_Rec_1496524,Human_Splice_Rec_1496532,Human_Splice_Rec_1496533,Human_Splice_Rec_1496536,Human_Splice_Rec_1496544,Human_Splice_Rec_1496545,Human_Splice_Rec_1496552,Human_Splice_Rec_1496553,Human_Splice_Rec_1496562 Human_miRNA_ID_2909295 RMVar_hsa_circ_9074,RMVar_hsa_circ_165333,RMVar_hsa_circ_77774 105022 RMVar_ID_105022 Human_SNP_ID_548027438 m1A Human chr14 - 23636443 23636443 23636443 TTACAGCTCTTAAAGGTGGCACGGACCCAACGAGTGAGCAGCAGCAAGATTTATCATGAAGACCA TTACAGCTCTTAAAGGTGGCACGGACCCAACGTGTGAGCAGCAGCAAGATTTATCATGAAGACCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23636393..23636539 26863196 MeRIP-seq:(Medium) rs1566697445 Functional Loss SNV dbSNP153 33..33 33 - - - 105023 RMVar_ID_105023 Human_SNP_ID_548028541 m1A Human chr14 - 23638986 23638986 23638986 AATCCAGCACTCACCCACTGGTGGACCCCGTGACCACGGCTACCCGGTTAGCCAGGACGCCCTTC AATCCAGCACTCACCCACTGGTGGACCCCGTGCCCACGGCTACCCGGTTAGCCAGGACGCCCTTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23638938..23639035 26863196 MeRIP-seq:(Medium) rs1346747354 Functional Loss SNV dbSNP153 33..33 33 - - - 105024 RMVar_ID_105024 Human_SNP_ID_548062440 m1A Human chr14 + 23764076 23764076 23764076 AAATAAATTAAAATTTGGTGACAGAGTTTGTCACTAAGAGGAAAAACTAGGGAGTGGGTGGAAAG AAATAAATTAAAATTTGGTGACAGAGTTTGTCTCTAAGAGGAAAAACTAGGGAGTGGGTGGAAAG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:23764054..23764181 26863196 MeRIP-seq:(Medium) rs764801999 Functional Loss SNV dbSNP153 33..33 33 - - - 105025 RMVar_ID_105025 Human_SNP_ID_548120916 m1A Human chr14 + 23988944 23988944 23988944 TGGAAGGAGTGGAACCCAGACTTGCTGGTCTGATCCATGCAGATGGCCAGGCTGCTAGGCCTCTG TGGAAGGAGTGGAACCCAGACTTGCTGGTCTGCTCCATGCAGATGGCCAGGCTGCTAGGCCTCTG A C DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:23970317..23989035 26863196 MeRIP-seq:(Medium) rs751575829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 105026 RMVar_ID_105026 Human_SNP_ID_548120944 m1A Human chr14 - 23988981 23988981 23988981 GGAGCTGGCCATCCGCACCGACTTCCGTGCCCAGGCACAGAGGCCTAGCAGCCTGGCCATCTGCA GGAGCTGGCCATCCGCACCGACTTCCGTGCCCTGGCACAGAGGCCTAGCAGCCTGGCCATCTGCA T A DHRS4-AS1 Ensembl:ENSG00000215256 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23988930..23989014 26863196 MeRIP-seq:(Medium) rs760956544 Functional Loss SNV dbSNP153 33..33 33 - - - 105027 RMVar_ID_105027 Human_SNP_ID_548120945 m1A Human chr14 - 23988981 23988981 23988981 GGAGCTGGCCATCCGCACCGACTTCCGTGCCCAGGCACAGAGGCCTAGCAGCCTGGCCATCTGCA GGAGCTGGCCATCCGCACCGACTTCCGTGCCCGGGCACAGAGGCCTAGCAGCCTGGCCATCTGCA T C DHRS4-AS1 Ensembl:ENSG00000215256 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23988930..23989014 26863196 MeRIP-seq:(Medium) rs760956544 Functional Loss SNV dbSNP153 33..33 33 - - - 105028 RMVar_ID_105028 Human_SNP_ID_548121522 m1A Human chr14 - 23990315 23990315 23990315 CCGCTCCCGGTCCTCCGCCTTCCCCACATGGCACACAGTGCCCGTCACGCTCAGCCCCTCCCCCT CCGCTCCCGGTCCTCCGCCTTCCCCACATGGCTCACAGTGCCCGTCACGCTCAGCCCCTCCCCCT T A DHRS4-AS1 Ensembl:ENSG00000215256 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:23990209..23990822;chr14:23988906..23990822;chr14:23990169..23990822 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 105029 RMVar_ID_105029 Human_SNP_ID_548126432 m1A Human chr14 + 24007119 24007119 24007119 ACTGTCTGGAGCGGGCTCGCCTCTGCGGCGGCACTCACCGCCCGGGCTTTACTGAAGCGGAGTCT ACTGTCTGGAGCGGGCTCGCCTCTGCGGCGGCCCTCACCGCCCGGGCTTTACTGAAGCGGAGTCT A C AL136419.1 Ensembl:ENSG00000285467 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:24007082..24007166;chr14:24007091..24007175;chr14:24007040..24007161 26863196 MeRIP-seq:(Medium) rs555880908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5418060 105030 RMVar_ID_105030 Human_SNP_ID_548140535 m1A Human chr14 - 24056579 24056579 24056579 GAGAGAGAAACGGGCCCAGTGAGGGGCAGGGCAGTGGGTGCAGGTGGCACAGAGTCAGGTTGGGG GAGAGAGAAACGGGCCCAGTGAGGGGCAGGGCGGTGGGTGCAGGTGGCACAGAGTCAGGTTGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24056570..24056662 26863196 MeRIP-seq:(Medium) rs1488059956 Functional Loss SNV dbSNP153 33..33 33 - - - 105031 RMVar_ID_105031 Human_SNP_ID_548151156 m1A Human chr14 - 24094376 24094376 24094376 CATGGCACCTGGGCAGGGGCTGCGGGGTGGCCAGGAACCGAGCGGAGCCGGGGAGGTATGGAAGG CATGGCACCTGGGCAGGGGCTGCGGGGTGGCCGGGAACCGAGCGGAGCCGGGGAGGTATGGAAGG T C NRL Ensembl:ENSG00000129535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:24094328..24094496;chr14:24094326..24094511 26863196 MeRIP-seq:(Medium) rs745821621 Functional Loss SNV dbSNP153 33..33 33 - - - 105032 RMVar_ID_105032 Human_SNP_ID_548151172 m1A Human chr14 - 24094415 24094415 24094415 GGGGGTCACTCACCGCAGGCCAGGGCGGTACAATGCGGCCATGGCACCTGGGCAGGGGCTGCGGG GGGGGTCACTCACCGCAGGCCAGGGCGGTACAGTGCGGCCATGGCACCTGGGCAGGGGCTGCGGG T C NRL Ensembl:ENSG00000129535 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24094355..24094456 32194978 MeRIP-seq:(Medium) rs1270151846 Functional Loss SNV dbSNP153 33..33 33 - - - 105033 RMVar_ID_105033 Human_SNP_ID_548151236 m1A Human chr14 - 24094575 24094575 24094575 CCTCCCAAGAGACGCGCGGCGCGGGAGGCTGGACCCACAGCAGTCGCCCCTGCCCGCCTCCGCCT CCTCCCAAGAGACGCGCGGCGCGGGAGGCTGGGCCCACAGCAGTCGCCCCTGCCCGCCTCCGCCT T C NRL Ensembl:ENSG00000129535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24094573..24094763 26863196 MeRIP-seq:(Medium) rs1473024738 Functional Loss SNV dbSNP153 33..33 33 - - - 105034 RMVar_ID_105034 Human_SNP_ID_548152305 m1A Human chr14 + 24098361 24098359 24098362 GATGTCCCCAGCTGATTTCCAGCGAGCTGTGGATGAGAGGTTTCCAGGCTGCATGCAGGGTAACC GATGTCCCCAGCTGATTTCCAGCGAGCTGTG___GAGAGGTTTCCAGGCTGCATGCAGGGTAACC GGAT G PCK2 Ensembl:ENSG00000100889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24098227..24098378 32194978 MeRIP-seq:(Medium) rs747610455 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18979315,Human_RBP_ID_21968939,Human_RBP_ID_22044983,Human_RBP_ID_22577052 Human_Splice_Rec_1497461,Human_Splice_Rec_1497481,Human_Splice_Rec_1497489,Human_Splice_Rec_1497501,Human_Splice_Rec_1497511,Human_Splice_Rec_1497517,Human_Splice_Rec_1497535,Human_Splice_Rec_1497543,Human_Splice_Rec_1497561,Human_Splice_Rec_1497597 RMVar_hsa_circ_24936,RMVar_hsa_circ_288178,RMVar_hsa_circ_19813,RMVar_hsa_circ_70747,RMVar_hsa_circ_369835,RMVar_hsa_circ_165347 105035 RMVar_ID_105035 Human_SNP_ID_548152307 m1A Human chr14 + 24098361 24098361 24098361 GATGTCCCCAGCTGATTTCCAGCGAGCTGTGGATGAGAGGTTTCCAGGCTGCATGCAGGGTAACC GATGTCCCCAGCTGATTTCCAGCGAGCTGTGGGTGAGAGGTTTCCAGGCTGCATGCAGGGTAACC A G PCK2 Ensembl:ENSG00000100889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24098227..24098378 32194978 MeRIP-seq:(Medium) rs1297152828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18979315,Human_RBP_ID_21968939,Human_RBP_ID_22044983,Human_RBP_ID_22577052 Human_Splice_Rec_1497461,Human_Splice_Rec_1497481,Human_Splice_Rec_1497489,Human_Splice_Rec_1497501,Human_Splice_Rec_1497511,Human_Splice_Rec_1497517,Human_Splice_Rec_1497535,Human_Splice_Rec_1497543,Human_Splice_Rec_1497561,Human_Splice_Rec_1497597 RMVar_hsa_circ_24936,RMVar_hsa_circ_288178,RMVar_hsa_circ_19813,RMVar_hsa_circ_70747,RMVar_hsa_circ_369835,RMVar_hsa_circ_165347 105036 RMVar_ID_105036 Human_SNP_ID_548152984 m1A Human chr14 - 24100193 24100193 24100193 CACCGCACATACCAGGTTTCCAGGGTTTGCCCAGCCAGGAGGTCACAGTAACACCAGGTGGAAGA CACCGCACATACCAGGTTTCCAGGGTTTGCCCGGCCAGGAGGTCACAGTAACACCAGGTGGAAGA T C NRL Ensembl:ENSG00000129535 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24100104..24100254 32194978 MeRIP-seq:(Medium) rs1271724041 Functional Loss SNV dbSNP153 33..33 33 - - - 105037 RMVar_ID_105037 Human_SNP_ID_548153723 m1A Human chr14 + 24103234 24103234 24103234 TGTTTGTGGGCAGCGCCATGCGCTCTGAGTCCACTGCTGCAGCAGAACACAAAGGTGAGCACCCT TGTTTGTGGGCAGCGCCATGCGCTCTGAGTCCGCTGCTGCAGCAGAACACAAAGGTGAGCACCCT A G PCK2 Ensembl:ENSG00000100889 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24103183..24103637 32194978 MeRIP-seq:(Medium) rs541220581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1497472,Human_Splice_Rec_1497473,Human_Splice_Rec_1497528,Human_Splice_Rec_1497529,Human_Splice_Rec_1497554,Human_Splice_Rec_1497555,Human_Splice_Rec_1497572,Human_Splice_Rec_1497573,Human_Splice_Rec_1497622,Human_Splice_Rec_1497623 RMVar_hsa_circ_24936,RMVar_hsa_circ_369835,RMVar_hsa_circ_165347,RMVar_hsa_circ_165349,RMVar_hsa_circ_371803 105038 RMVar_ID_105038 Human_SNP_ID_548156668 m1A Human chr14 - 24114863 24114863 24114863 GGCGCGAGGCCTTGTTTACACCGACTGCCGCCACTGCGTTGGCCAACCGCTCCTCCGTCACGCGC GGCGCGAGGCCTTGTTTACACCGACTGCCGCCGCTGCGTTGGCCAACCGCTCCTCCGTCACGCGC T C NRL Ensembl:ENSG00000129535 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24114815..24114989 26863196 MeRIP-seq:(Medium) rs573881980 Functional Loss SNV dbSNP153 33..33 33 - - - 105039 RMVar_ID_105039 Human_SNP_ID_548156669 m1A Human chr14 - 24114863 24114863 24114863 GGCGCGAGGCCTTGTTTACACCGACTGCCGCCACTGCGTTGGCCAACCGCTCCTCCGTCACGCGC GGCGCGAGGCCTTGTTTACACCGACTGCCGCCCCTGCGTTGGCCAACCGCTCCTCCGTCACGCGC T G NRL Ensembl:ENSG00000129535 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24114815..24114989 26863196 MeRIP-seq:(Medium) rs573881980 Functional Loss SNV dbSNP153 33..33 33 - - - 105040 RMVar_ID_105040 Human_SNP_ID_548156919 m1A Human chr14 - 24115601 24115601 24115601 GGACCCGGATCCTGCACTGCTGCTGTTCCGCGATCCCATCTTCTGGTCACAGCATTCTTAGGTCC GGACCCGGATCCTGCACTGCTGCTGTTCCGCGGTCCCATCTTCTGGTCACAGCATTCTTAGGTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24115551..24115680 26863196 MeRIP-seq:(Medium) rs750939495 Functional Loss SNV dbSNP153 33..33 33 - - - 105041 RMVar_ID_105041 Human_SNP_ID_548156976 m1A Human chr14 + 24115701 24115701 24115701 TGGCCTGCGTCGGAGTGAGGAAGAGGAAGAAGAGGATGAAGATGTGGATCTGGCCCAGGTACTGG TGGCCTGCGTCGGAGTGAGGAAGAGGAAGAAGCGGATGAAGATGTGGATCTGGCCCAGGTACTGG A C DCAF11 Ensembl:ENSG00000100897 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24115398..24115767 26863196 MeRIP-seq:(Medium) rs1433425530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9368579,Human_RBP_ID_18980297,Human_RBP_ID_22926332,Human_RBP_ID_24543798,Human_RBP_ID_26324931 Human_Splice_Rec_1497633,Human_Splice_Rec_1497639,Human_Splice_Rec_1497643,Human_Splice_Rec_1497671,Human_Splice_Rec_1497675,Human_Splice_Rec_1497683,Human_Splice_Rec_1497689,Human_Splice_Rec_1497701,Human_Splice_Rec_1497729,Human_Splice_Rec_1497759,Human_Splice_Rec_1497763,Human_Splice_Rec_1497771,Human_Splice_Rec_1497779,Human_Splice_Rec_1497785,Human_Splice_Rec_1497799,Human_Splice_Rec_1497807,Human_Splice_Rec_1497815,Human_Splice_Rec_1497821,Human_Splice_Rec_1497825,Human_Splice_Rec_1497835,Human_Splice_Rec_1497845,Human_Splice_Rec_1497853,Human_Splice_Rec_1497859,Human_Splice_Rec_1497863,Human_Splice_Rec_1497889,Human_Splice_Rec_1497893,Human_Splice_Rec_1497899,Human_Splice_Rec_1497903,Human_Splice_Rec_1497909,Human_Splice_Rec_1497915,Human_Splice_Rec_1497943,Human_Splice_Rec_1497969,Human_Splice_Rec_1497975 105042 RMVar_ID_105042 Human_SNP_ID_548162517 m1A Human chr14 - 24136255 24136255 24136255 CGGGCTGGACCCTGAGCATGGCCATGACCGGGACGGGGGGCCTAGCGCCGCACAAGGAGTGGAGT CGGGCTGGACCCTGAGCATGGCCATGACCGGGTCGGGGGGCCTAGCGCCGCACAAGGAGTGGAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:24136176..24136336;chr14:24136176..24136330;chr14:24136201..24136347 26863196 MeRIP-seq:(Medium) rs1171121476 Functional Loss SNV dbSNP153 33..33 33 - - - 105043 RMVar_ID_105043 Human_SNP_ID_548162518 m1A Human chr14 - 24136255 24136255 24136255 CGGGCTGGACCCTGAGCATGGCCATGACCGGGACGGGGGGCCTAGCGCCGCACAAGGAGTGGAGT CGGGCTGGACCCTGAGCATGGCCATGACCGGGGCGGGGGGCCTAGCGCCGCACAAGGAGTGGAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:24136176..24136336;chr14:24136176..24136330;chr14:24136201..24136347 26863196 MeRIP-seq:(Medium) rs1171121476 Functional Loss SNV dbSNP153 33..33 33 - - - 105044 RMVar_ID_105044 Human_SNP_ID_548162530 m1A Human chr14 + 24136275 24136275 24136275 CTAGGCCCCCCGTCCCGGTCATGGCCATGCTCAGGGTCCAGCCCGAGGCCCAAGCCAAGGTGAGC CTAGGCCCCCCGTCCCGGTCATGGCCATGCTCGGGGTCCAGCCCGAGGCCCAAGCCAAGGTGAGC A G PSME1 Ensembl:ENSG00000092010 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24136225..24136337 26863196 MeRIP-seq:(Medium) rs756891588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443988,Human_RBP_ID_758090,Human_RBP_ID_4308227,Human_RBP_ID_9323741 Human_Splice_Rec_1498037,Human_Splice_Rec_1498055,Human_Splice_Rec_1498073,Human_Splice_Rec_1498079,Human_Splice_Rec_1498095,Human_Splice_Rec_1498111,Human_Splice_Rec_1498127 RMVar_hsa_circ_60570 105045 RMVar_ID_105045 Human_SNP_ID_548163126 m1A Human chr14 + 24138116 24138112 24138116 TGAGGATGGTAACAATTTTGGAGTGGCTGTCCAGGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT TGAGGATGGTAACAATTTTGGAGTGGCTG____GGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT GTCCA G PSME1 Ensembl:ENSG00000092010 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24138026..24138125 32194978 MeRIP-seq:(Medium) rs372750711 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_9368605,Human_RBP_ID_17856384,Human_RBP_ID_19063760,Human_RBP_ID_26324627 Human_Splice_Rec_1498046,Human_Splice_Rec_1498047,Human_Splice_Rec_1498064,Human_Splice_Rec_1498065,Human_Splice_Rec_1498078,Human_Splice_Rec_1498088,Human_Splice_Rec_1498104,Human_Splice_Rec_1498105,Human_Splice_Rec_1498120,Human_Splice_Rec_1498121,Human_Splice_Rec_1498138,Human_Splice_Rec_1498148,Human_Splice_Rec_1498149,Human_Splice_Rec_1498154,Human_Splice_Rec_1498155 RMVar_hsa_circ_90904,RMVar_hsa_circ_83404,RMVar_hsa_circ_165352,RMVar_hsa_circ_96832,RMVar_hsa_circ_165353,RMVar_hsa_circ_335698,RMVar_hsa_circ_165354,RMVar_hsa_circ_165355 105046 RMVar_ID_105046 Human_SNP_ID_548163129 m1A Human chr14 + 24138116 24138116 24138116 TGAGGATGGTAACAATTTTGGAGTGGCTGTCCAGGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT TGAGGATGGTAACAATTTTGGAGTGGCTGTCCCGGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT A C PSME1 Ensembl:ENSG00000092010 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24138026..24138125 32194978 MeRIP-seq:(Medium) rs759503525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9368605,Human_RBP_ID_17856384,Human_RBP_ID_19063760,Human_RBP_ID_26324627 Human_Splice_Rec_1498046,Human_Splice_Rec_1498047,Human_Splice_Rec_1498064,Human_Splice_Rec_1498065,Human_Splice_Rec_1498078,Human_Splice_Rec_1498088,Human_Splice_Rec_1498104,Human_Splice_Rec_1498105,Human_Splice_Rec_1498120,Human_Splice_Rec_1498121,Human_Splice_Rec_1498138,Human_Splice_Rec_1498148,Human_Splice_Rec_1498149,Human_Splice_Rec_1498154,Human_Splice_Rec_1498155 RMVar_hsa_circ_90904,RMVar_hsa_circ_83404,RMVar_hsa_circ_165352,RMVar_hsa_circ_96832,RMVar_hsa_circ_165353,RMVar_hsa_circ_335698,RMVar_hsa_circ_165354,RMVar_hsa_circ_165355 105047 RMVar_ID_105047 Human_SNP_ID_548163271 m1A Human chr14 + 24138514 24138514 24138514 TCGGCAGCTGGTGCACGAGCTGGATGAGGCAGAGTACCGGGACATCCGGCTGATGGTCATGGAGA TCGGCAGCTGGTGCACGAGCTGGATGAGGCAGGGTACCGGGACATCCGGCTGATGGTCATGGAGA A G PSME1 Ensembl:ENSG00000092010 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24138390..24138558 26863196 MeRIP-seq:(Medium) rs776195032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443991,Human_RBP_ID_8798089,Human_RBP_ID_9369848,Human_RBP_ID_18980310,Human_RBP_ID_26807992 Human_Splice_Rec_1498052,Human_Splice_Rec_1498053,Human_Splice_Rec_1498070,Human_Splice_Rec_1498071,Human_Splice_Rec_1498092,Human_Splice_Rec_1498093,Human_Splice_Rec_1498110,Human_Splice_Rec_1498126,Human_Splice_Rec_1498142,Human_Splice_Rec_1498143,Human_Splice_Rec_1498160,Human_Splice_Rec_1498161 RMVar_hsa_circ_54502,RMVar_hsa_circ_90904,RMVar_hsa_circ_96832,RMVar_hsa_circ_165353,RMVar_hsa_circ_165355,RMVar_hsa_circ_81571,RMVar_hsa_circ_8459,RMVar_hsa_circ_91510,RMVar_hsa_circ_165356,RMVar_hsa_circ_165357 105048 RMVar_ID_105048 Human_SNP_ID_548163272 m1A Human chr14 + 24138514 24138514 24138514 TCGGCAGCTGGTGCACGAGCTGGATGAGGCAGAGTACCGGGACATCCGGCTGATGGTCATGGAGA TCGGCAGCTGGTGCACGAGCTGGATGAGGCAGTGTACCGGGACATCCGGCTGATGGTCATGGAGA A T PSME1 Ensembl:ENSG00000092010 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24138390..24138558 26863196 MeRIP-seq:(Medium) rs776195032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443991,Human_RBP_ID_8798089,Human_RBP_ID_9369848,Human_RBP_ID_18980310,Human_RBP_ID_26807992 Human_Splice_Rec_1498052,Human_Splice_Rec_1498053,Human_Splice_Rec_1498070,Human_Splice_Rec_1498071,Human_Splice_Rec_1498092,Human_Splice_Rec_1498093,Human_Splice_Rec_1498110,Human_Splice_Rec_1498126,Human_Splice_Rec_1498142,Human_Splice_Rec_1498143,Human_Splice_Rec_1498160,Human_Splice_Rec_1498161 RMVar_hsa_circ_54502,RMVar_hsa_circ_90904,RMVar_hsa_circ_96832,RMVar_hsa_circ_165353,RMVar_hsa_circ_165355,RMVar_hsa_circ_81571,RMVar_hsa_circ_8459,RMVar_hsa_circ_91510,RMVar_hsa_circ_165356,RMVar_hsa_circ_165357 105049 RMVar_ID_105049 Human_SNP_ID_548163425 m1A Human chr14 - 24138947 24138947 24138947 AGAGACTTGGGCTGATGGGCAGTGGTATAACTATATTTATTGTGCCTGAGAGGCAAGGTGAGGGA AGAGACTTGGGCTGATGGGCAGTGGTATAACTGTATTTATTGTGCCTGAGAGGCAAGGTGAGGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24138726..24138950 32194978 MeRIP-seq:(Medium) rs762255035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2409553 105050 RMVar_ID_105050 Human_SNP_ID_548163496 m1A Human chr14 + 24139119 24139119 24139119 GCCGGATGTCATCAAGGTGGCAGTCAAAGTCCACAAGGTGCTGGTGGGCCCGATCTTCCAGTAGA GCCGGATGTCATCAAGGTGGCAGTCAAAGTCCGCAAGGTGCTGGTGGGCCCGATCTTCCAGTAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:24139069..24139183 26863196 MeRIP-seq:(Medium) rs1164443557 Functional Loss SNV dbSNP153 33..33 33 - - - 105051 RMVar_ID_105051 Human_SNP_ID_548165894 m1A Human chr14 - 24147037 24147037 24147037 CGCTCTCTTCTAAGAGCTGCTAGTCCTTCTCCACCCCAGGCGCTCCCTCTGGCTGCCCCTCCCAC CGCTCTCTTCTAAGAGCTGCTAGTCCTTCTCCGCCCCAGGCGCTCCCTCTGGCTGCCCCTCCCAC T C PSME2 Ensembl:ENSG00000100911 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24146987..24147088 26863196 MeRIP-seq:(Medium) rs1566611043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3445004,Human_RBP_ID_5127559,Human_RBP_ID_17076329,Human_RBP_ID_18936648,Human_RBP_ID_21968944 RMVar_hsa_circ_92052,RMVar_hsa_circ_165358 105052 RMVar_ID_105052 Human_SNP_ID_548166076 m1A Human chr14 + 24147601 24147600 24147601 CTGGGGCGGCTGCGTGGGCCGGGGTGGGCCTCAAAGCCGGGCACCAGACGGGAGGGGCGGCGCTC CTGGGGCGGCTGCGTGGGCCGGGGTGGGCCTC_AAGCCGGGCACCAGACGGGAGGGGCGGCGCTC CA C RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:24147551..24147708 26863196 MeRIP-seq:(Medium) rs970380198 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4290057,Human_RBP_ID_9352978,Human_RBP_ID_18417916 105053 RMVar_ID_105053 Human_SNP_ID_548167239 m1A Human chr14 + 24150765 24150765 24150765 CCCCGGCCCTATGCCAGCTCTTTGGAAAAGGGACCCCCCAAGCCTGGGCCCCCACGACGCCTTAG CCCCGGCCCTATGCCAGCTCTTTGGAAAAGGGTCCCCCCAAGCCTGGGCCCCCACGACGCCTTAG A T RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24150719..24150900 26863196 MeRIP-seq:(Medium) rs1320466908 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_8402258 Human_miRNA_ID_2193394,Human_miRNA_ID_2207607 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 105054 RMVar_ID_105054 Human_SNP_ID_548167271 m1A Human chr14 + 24150847 24150847 24150847 CCTGTGGAGATCCTGAGAAGCAGCGCCAAGACAAGATGCGGGAAGAAGGCCTCCAGCTAGTGAGC CCTGTGGAGATCCTGAGAAGCAGCGCCAAGACCAGATGCGGGAAGAAGGCCTCCAGCTAGTGAGC A C RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24150796..24150908 26863196 MeRIP-seq:(Medium) rs758681145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230947,Human_RBP_ID_18979365,Human_RBP_ID_26324640,Human_RBP_ID_27808735 Human_Splice_Rec_1498475,Human_Splice_Rec_1498515,Human_Splice_Rec_1498585,Human_Splice_Rec_1498619,Human_Splice_Rec_1498731 Human_miRNA_ID_1966211,Human_miRNA_ID_2361668 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 105055 RMVar_ID_105055 Human_SNP_ID_548167442 m1A Human chr14 + 24151351 24151351 24151351 GGATCGTCATGGCAACCTTGATGAAGCTGTGGAGGAGTGTGTGAGGACCAGGCGAAGGAAGGTAT GGATCGTCATGGCAACCTTGATGAAGCTGTGGGGGAGTGTGTGAGGACCAGGCGAAGGAAGGTAT A G RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24151260..24151400 26863196 MeRIP-seq:(Medium) rs1422552782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_813732,Human_RBP_ID_880493,Human_RBP_ID_5522631,Human_RBP_ID_9368631,Human_RBP_ID_18979369,Human_RBP_ID_26324643 Human_Splice_Rec_1498477,Human_Splice_Rec_1498517,Human_Splice_Rec_1498586,Human_Splice_Rec_1498587,Human_Splice_Rec_1498621,Human_Splice_Rec_1498645,Human_Splice_Rec_1498733 Human_miRNA_ID_2450647,Human_miRNA_ID_2540093,Human_miRNA_ID_2708806 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 105056 RMVar_ID_105056 Human_SNP_ID_548176529 m1A Human chr14 + 24180750 24180750 24180750 AGGCTGCAGATACGCAGAAGCTCGGGAGCCACATCTATAACCTGTGAGGAAAGAGTGGCTGACTC AGGCTGCAGATACGCAGAAGCTCGGGAGCCACGTCTATAACCTGTGAGGAAAGAGTGGCTGACTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24180676..24180775 32194978 MeRIP-seq:(Medium) rs755169376 Functional Loss SNV dbSNP153 33..33 33 - - - 105057 RMVar_ID_105057 Human_SNP_ID_548177067 m1A Human chr14 - 24182375 24182375 24182375 ACAGGCTGAATACGACGCCATGTTGCTGGAGCACGCTGGAGAGGCCATCCCTGCCCTGGCAGCCG ACAGGCTGAATACGACGCCATGTTGCTGGAGCGCGCTGGAGAGGCCATCCCTGCCCTGGCAGCCG T C IPO4,AL136295.4 Ensembl:ENSG00000196497,Ensembl:ENSG00000259522 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24182326..24182425 26863196 MeRIP-seq:(Medium) rs965727462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6335448,Human_RBP_ID_22438667 Human_Splice_Rec_1499106,Human_Splice_Rec_1499107,Human_Splice_Rec_1499162,Human_Splice_Rec_1499163,Human_Splice_Rec_1499190,Human_Splice_Rec_1499191,Human_Splice_Rec_1499246,Human_Splice_Rec_1499247,Human_Splice_Rec_1499304,Human_Splice_Rec_1499305,Human_Splice_Rec_1499362,Human_Splice_Rec_1499363,Human_Splice_Rec_1499418,Human_Splice_Rec_1499419,Human_Splice_Rec_1499476,Human_Splice_Rec_1499477,Human_Splice_Rec_1499492,Human_Splice_Rec_1499493,Human_Splice_Rec_1499544,Human_Splice_Rec_1499545,Human_Splice_Rec_1499666,Human_Splice_Rec_1499667 Human_miRNA_ID_1193877,Human_miRNA_ID_1193878,Human_miRNA_ID_1372847,Human_miRNA_ID_1372848 RMVar_hsa_circ_77851,RMVar_hsa_circ_116127,RMVar_hsa_circ_100083,RMVar_hsa_circ_111283,RMVar_hsa_circ_165379,RMVar_hsa_circ_165380,RMVar_hsa_circ_165381,RMVar_hsa_circ_82005,RMVar_hsa_circ_165382,RMVar_hsa_circ_165383 105058 RMVar_ID_105058 Human_SNP_ID_548177278 m1A Human chr14 + 24182956 24182956 24182956 CCCAACCGAGGCCCAGCACCTCTCCTTCCCGAAGCCCACCTGCCCTGCTCACCTTCCTCTGCAGC CCCAACCGAGGCCCAGCACCTCTCCTTCCCGAGGCCCACCTGCCCTGCTCACCTTCCTCTGCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24182952..24183044 26863196 MeRIP-seq:(Medium) rs1356880906 Functional Loss SNV dbSNP153 33..33 33 - - - 105059 RMVar_ID_105059 Human_SNP_ID_548177296 m1A Human chr14 + 24183006 24183004 24183006 ACCTTCCTCTGCAGCACAGCCTTGAGCACGCCACAGAGCTCAGCGAGGCGCCCAGGGGGCTTCAG ACCTTCCTCTGCAGCACAGCCTTGAGCACGC__CAGAGCTCAGCGAGGCGCCCAGGGGGCTTCAG CCA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24182983..24183133 32194978 MeRIP-seq:(Medium) rs748100178 Functional Loss DEL dbSNP153 32..33 33 - - - 105060 RMVar_ID_105060 Human_SNP_ID_548179627 m1A Human chr14 - 24188765 24188765 24188765 AGTTGCTGCCATGGAGTCAGCCGGGCTAGAGCAGCTCCTACGGGAGCTGCTGCTACCGGACACCG AGTTGCTGCCATGGAGTCAGCCGGGCTAGAGCGGCTCCTACGGGAGCTGCTGCTACCGGACACCG T C IPO4,AL136295.4 Ensembl:ENSG00000196497,Ensembl:ENSG00000259522 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24188714..24188783 26863196 MeRIP-seq:(Medium) rs769712901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4307842,Human_RBP_ID_5141072,Human_RBP_ID_18417917 Human_Splice_Rec_1499059,Human_Splice_Rec_1499117,Human_Splice_Rec_1499257,Human_Splice_Rec_1499315,Human_Splice_Rec_1499429,Human_Splice_Rec_1499501,Human_Splice_Rec_1499563,Human_Splice_Rec_1499575,Human_Splice_Rec_1499583,Human_Splice_Rec_1499591,Human_Splice_Rec_1499599,Human_Splice_Rec_1499605,Human_Splice_Rec_1499611,Human_Splice_Rec_1499615,Human_Splice_Rec_1499619 RMVar_hsa_circ_80148,RMVar_hsa_circ_165386 105061 RMVar_ID_105061 Human_SNP_ID_548181718 m1A Human chr14 - 24195564 24195564 24195564 GCTGGGCCGGGCCTCCAGATGGAGAAGGCGCAACGGGGAGTTCTTGAGTAAGCCAGAGCGGTGTC GCTGGGCCGGGCCTCCAGATGGAGAAGGCGCAGCGGGGAGTTCTTGAGTAAGCCAGAGCGGTGTC T C TM9SF1,AL136295.1 Ensembl:ENSG00000100926,Ensembl:ENSG00000254692 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24195516..24195631 26863196 MeRIP-seq:(Medium) rs1278330059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4308241 Human_Splice_Rec_1499743 RMVar_hsa_circ_125406,RMVar_hsa_circ_165388 105062 RMVar_ID_105062 Human_SNP_ID_548183695 m1A Human chr14 + 24201782 24201782 24201782 TGGTGGGAGCAGGAGCAAGAGGGCAAAGGGGGAGGTGCTACACACTTTTTAAAATGACCACATCT TGGTGGGAGCAGGAGCAAGAGGGCAAAGGGGGCGGTGCTACACACTTTTTAAAATGACCACATCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:24201731..24201846;chr14:24201741..24201843 26863196 MeRIP-seq:(Medium) rs921904478 Functional Loss SNV dbSNP153 33..33 33 - - - 105063 RMVar_ID_105063 Human_SNP_ID_548192300 m1A Human chr14 - 24232317 24232317 24232317 CAAGAGTGCTGGAGGGCGGCAGCGGCGACCGGAGCGGTAGGAGCAGCAATTTATCCGTGTGCAGC CAAGAGTGCTGGAGGGCGGCAGCGGCGACCGGTGCGGTAGGAGCAGCAATTTATCCGTGTGCAGC T A NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:24232195..24232375;chr14:24232276..24232350;chr14:24232208..24232375;chr14:24232186..24232400;chr14:24232187..24232375 26863196 MeRIP-seq:(Medium) rs901793409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231719,Human_RBP_ID_757932,Human_RBP_ID_4308243,Human_RBP_ID_5112343,Human_RBP_ID_22439557,Human_RBP_ID_27808743 Human_Splice_Rec_1499945,Human_Splice_Rec_1499959,Human_Splice_Rec_1499971,Human_Splice_Rec_1499983,Human_Splice_Rec_1499997,Human_Splice_Rec_1500003,Human_Splice_Rec_1500015,Human_Splice_Rec_1500027,Human_Splice_Rec_1500029,Human_Splice_Rec_1500033 105064 RMVar_ID_105064 Human_SNP_ID_548192448 m1A Human chr14 - 24232517 24232517 24232517 TCGCTAGCCCGGGCTCGCCAGGGACTCTCAGAATCGCAGAGTCGTCATCTCTGCTGTTGCTAAAC TCGCTAGCCCGGGCTCGCCAGGGACTCTCAGAGTCGCAGAGTCGTCATCTCTGCTGTTGCTAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24232466..24232569 26863196 MeRIP-seq:(Medium) rs1195004760 Functional Loss SNV dbSNP153 33..33 33 - - - 105065 RMVar_ID_105065 Human_SNP_ID_548192596 m1A Human chr14 + 24233005 24233005 24233005 GCGGGGTAAGGAATGCACCGTCAGGGTCTCTCACAACCCTTTCCCAGCTCTCCTCCCCAACAAAC GCGGGGTAAGGAATGCACCGTCAGGGTCTCTCTCAACCCTTTCCCAGCTCTCCTCCCCAACAAAC A T GMPR2 Ensembl:ENSG00000100938 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24232993..24233144 32194978 MeRIP-seq:(Medium) rs1309256476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5494137,Human_RBP_ID_18417920 105066 RMVar_ID_105066 Human_SNP_ID_548193973 m1A Human chr14 - 24238295 24238292 24238296 CCATCCCTCTCGATGAGCTCACCACCTGACTCACTGTGCCCAGCCAGCATGCCACCCAGCATCAC CCATCCCTCTCGATGAGCTCACCACCTGACT____GTGCCCAGCCAGCATGCCACCCAGCATCAC CAGTG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr14:24238248..24238379;chr14:24238226..24238425 26863196,32194978 MeRIP-seq:(Medium) rs1345742631 Functional Loss DEL dbSNP153 32..35 33 - - - 105067 RMVar_ID_105067 Human_SNP_ID_548197324 m1A Human chr14 - 24249708 24249708 24249708 CAGCTGGTGGGTGGCTGCTGAGCTGGCTATGCAGAGGCGCCCTGGGGATCCTGGTCTTGGGTGTG CAGCTGGTGGGTGGCTGCTGAGCTGGCTATGCGGAGGCGCCCTGGGGATCCTGGTCTTGGGTGTG T C TGM1 Ensembl:ENSG00000092295 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24249704..24249792 26863196 MeRIP-seq:(Medium) rs1453127376 Functional Loss SNV dbSNP153 33..33 33 - - - 105068 RMVar_ID_105068 Human_SNP_ID_548202346 m1A Human chr14 - 24266519 24266519 24266519 GCCTGTCCTGCCTCCCTGCCCTCCCTGCCCCCAGGTGCTGCAGGCCAGTGATAATGCCATAGAGT GCCTGTCCTGCCTCCCTGCCCTCCCTGCCCCCGGGTGCTGCAGGCCAGTGATAATGCCATAGAGT T C RABGGTA Ensembl:ENSG00000100949 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24266493..24266667 26863196 MeRIP-seq:(Medium) rs368048502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757040,Human_RBP_ID_880865,Human_RBP_ID_19063856,Human_RBP_ID_22648323 Human_Splice_Rec_1500539,Human_Splice_Rec_1500547,Human_Splice_Rec_1500575,Human_Splice_Rec_1500605,Human_Splice_Rec_1500615,Human_Splice_Rec_1500645,Human_Splice_Rec_1500677,Human_Splice_Rec_1500709,Human_Splice_Rec_1500725,Human_Splice_Rec_1500753 RMVar_hsa_circ_81864,RMVar_hsa_circ_115676,RMVar_hsa_circ_84730,RMVar_hsa_circ_110070,RMVar_hsa_circ_120975,RMVar_hsa_circ_165404,RMVar_hsa_circ_165406,RMVar_hsa_circ_165405,RMVar_hsa_circ_126885,RMVar_hsa_circ_270717,RMVar_hsa_circ_110551,RMVar_hsa_circ_165409,RMVar_hsa_circ_165413,RMVar_hsa_circ_105209,RMVar_hsa_circ_105468,RMVar_hsa_circ_165415,RMVar_hsa_circ_84440,RMVar_hsa_circ_165414,RMVar_hsa_circ_165411,RMVar_hsa_circ_165412,RMVar_hsa_circ_165410,RMVar_hsa_circ_165408 105069 RMVar_ID_105069 Human_SNP_ID_548204074 m1A Human chr14 - 24271250 24271250 24271250 AGGACCTCTTTACACTCTGGGGGTCTCTGCCCAGGCACGCTTGCTGCTTCCGGACACAGCTGTGG AGGACCTCTTTACACTCTGGGGGTCTCTGCCCGGGCACGCTTGCTGCTTCCGGACACAGCTGTGG T C RABGGTA Ensembl:ENSG00000100949 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24271237..24271521 26863196 MeRIP-seq:(Medium) rs540093542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84730,RMVar_hsa_circ_165404 105070 RMVar_ID_105070 Human_SNP_ID_548204083 m1A Human chr14 + 24271265 24271265 24271265 GAAGCAGCAAGCGTGCCTGGGCAGAGACCCCCAGAGTGTAAAGAGGTCCTGGGACAGGCTTTGCA GAAGCAGCAAGCGTGCCTGGGCAGAGACCCCCGGAGTGTAAAGAGGTCCTGGGACAGGCTTTGCA A G AL096870.10 Ensembl:ENSG00000288044 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24271185..24271561 26863196 MeRIP-seq:(Medium) rs1566389526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1500845 105071 RMVar_ID_105071 Human_SNP_ID_548205555 m1A Human chr14 - 24277033 24277033 24277033 ACTCTCCATGCCCACTGCCCCCCCACAGCCACAGGGACATTCATGTGGATTCTAGGTTCTGCCAG ACTCTCCATGCCCACTGCCCCCCCACAGCCACGGGGACATTCATGTGGATTCTAGGTTCTGCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:24277002..24277322 26863196 MeRIP-seq:(Medium) rs1310096703 Functional Loss SNV dbSNP153 33..33 33 - - - 105072 RMVar_ID_105072 Human_SNP_ID_548209079 m1A Human chr14 - 24292373 24292373 24292373 AGTAGAAGCAGAGAGGGCAGGGCAGGAAAGTGACATGGCTAGGTGGCTCTTACCCTGCCTTCCGC AGTAGAAGCAGAGAGGGCAGGGCAGGAAAGTGCCATGGCTAGGTGGCTCTTACCCTGCCTTCCGC T G DHRS1 Ensembl:ENSG00000157379 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24292353..24292468 26863196 MeRIP-seq:(Medium) rs1398029723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_882990,Human_RBP_ID_5351374,Human_RBP_ID_22539931,Human_RBP_ID_22648813 RMVar_hsa_circ_124443,RMVar_hsa_circ_118674,RMVar_hsa_circ_165426,RMVar_hsa_circ_88023,RMVar_hsa_circ_165425,RMVar_hsa_circ_165428 105073 RMVar_ID_105073 Human_SNP_ID_548210936 m1A Human chr14 + 24299955 24299955 24299955 GCTTTTGCAGCCGGACAGGTCGCGAAGCACACATGGGGCAGGGTCCGCGCTCTCCACACAAGGTG GCTTTTGCAGCCGGACAGGTCGCGAAGCACACGTGGGGCAGGGTCCGCGCTCTCCACACAAGGTG A G NOP9 Ensembl:ENSG00000196943 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24299904..24300003 26863196 MeRIP-seq:(Medium) rs768384595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757462,Human_RBP_ID_813431,Human_RBP_ID_4290592,Human_RBP_ID_5463780 RMVar_hsa_circ_123380,RMVar_hsa_circ_165433,RMVar_hsa_circ_81140,RMVar_hsa_circ_165432 105074 RMVar_ID_105074 Human_SNP_ID_548210939 m1A Human chr14 + 24299962 24299962 24299962 CAGCCGGACAGGTCGCGAAGCACACATGGGGCAGGGTCCGCGCTCTCCACACAAGGTGGGGCGCC CAGCCGGACAGGTCGCGAAGCACACATGGGGCCGGGTCCGCGCTCTCCACACAAGGTGGGGCGCC A C NOP9 Ensembl:ENSG00000196943 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24299913..24299994 26863196 MeRIP-seq:(Medium) rs1411826239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757462,Human_RBP_ID_4308664 RMVar_hsa_circ_123380,RMVar_hsa_circ_165433,RMVar_hsa_circ_81140,RMVar_hsa_circ_165432 105075 RMVar_ID_105075 Human_SNP_ID_548210940 m1A Human chr14 + 24299962 24299962 24299962 CAGCCGGACAGGTCGCGAAGCACACATGGGGCAGGGTCCGCGCTCTCCACACAAGGTGGGGCGCC CAGCCGGACAGGTCGCGAAGCACACATGGGGCGGGGTCCGCGCTCTCCACACAAGGTGGGGCGCC A G NOP9 Ensembl:ENSG00000196943 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24299913..24299994 26863196 MeRIP-seq:(Medium) rs1411826239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757462,Human_RBP_ID_4308664 RMVar_hsa_circ_123380,RMVar_hsa_circ_165433,RMVar_hsa_circ_81140,RMVar_hsa_circ_165432 105076 RMVar_ID_105076 Human_SNP_ID_548215251 m1A Human chr14 + 24313139 24313139 24313139 CTGGTCCTGGGTGTGGGGAAGAAAGGCCATCAAGGTAGATGCGGGTGGGGAACAGCTTGAGAGAG CTGGTCCTGGGTGTGGGGAAGAAAGGCCATCAGGGTAGATGCGGGTGGGGAACAGCTTGAGAGAG A G LTB4R Ensembl:ENSG00000213903 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24313088..24313172 26863196 MeRIP-seq:(Medium) rs183092486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757890,Human_RBP_ID_6335850,Human_RBP_ID_12306221,Human_RBP_ID_17067559,Human_RBP_ID_22923016,Human_RBP_ID_23617185 105077 RMVar_ID_105077 Human_SNP_ID_548216379 m1A Human chr14 + 24316783 24316783 24316783 TAGCTCTGAGCCAGTTCAGTACCTGGAGGAGGAGCAGGGGCGTGGAGGGCGTGGAGGGCGTGGGA TAGCTCTGAGCCAGTTCAGTACCTGGAGGAGGGGCAGGGGCGTGGAGGGCGTGGAGGGCGTGGGA A G LTB4R Ensembl:ENSG00000213903 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24316734..24316895 26863196 MeRIP-seq:(Medium) rs1382020056 Functional Loss SNV dbSNP153 33..33 33 - - - 105078 RMVar_ID_105078 Human_SNP_ID_548232180 m1A Human chr14 + 24370560 24370560 24370560 ACCTGGCAGTGCCCTCCCCACTCGCTTGGTCCAAGGCCCGGATTGGGGGACACAGCCCTATCTTC ACCTGGCAGTGCCCTCCCCACTCGCTTGGTCCGAGGCCCGGATTGGGGGACACAGCCCTATCTTC A G NFATC4 Ensembl:ENSG00000100968 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24370391..24370575 32194978 MeRIP-seq:(Medium) rs1268244046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5257867 Human_Splice_Rec_1501475,Human_Splice_Rec_1501481,Human_Splice_Rec_1501499,Human_Splice_Rec_1501519,Human_Splice_Rec_1501529,Human_Splice_Rec_1501549,Human_Splice_Rec_1501569,Human_Splice_Rec_1501585,Human_Splice_Rec_1501601,Human_Splice_Rec_1501619,Human_Splice_Rec_1501637,Human_Splice_Rec_1501655,Human_Splice_Rec_1501677,Human_Splice_Rec_1501707,Human_Splice_Rec_1501725,Human_Splice_Rec_1501741,Human_Splice_Rec_1501757,Human_Splice_Rec_1501775,Human_Splice_Rec_1501791,Human_Splice_Rec_1501807,Human_Splice_Rec_1501823,Human_Splice_Rec_1501841 RMVar_hsa_circ_90528,RMVar_hsa_circ_88243,RMVar_hsa_circ_165438,RMVar_hsa_circ_165439 105079 RMVar_ID_105079 Human_SNP_ID_548248001 m1A Human chr14 - 24430308 24430308 24430308 TGGGGGCCCTGGTCTGCCATTTCCAAGGTTCAAGCCACTCCCACCCCTCCCCCAGCCGTCCGCTG TGGGGGCCCTGGTCTGCCATTTCCAAGGTTCAGGCCACTCCCACCCCTCCCCCAGCCGTCCGCTG T C CBLN3 Ensembl:ENSG00000139899 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24430298..24430398 26863196 MeRIP-seq:(Medium) rs1383707139 Functional Loss SNV dbSNP153 33..33 33 - - - 105080 RMVar_ID_105080 Human_SNP_ID_548248184 m1A Human chr14 + 24430913 24430913 24430913 CACATCTGGCTGCAGCTGGAGGGCCCCAAGGAAAACGCCAGCAGAGCCAAGGTGAACGCCTTCTC CACATCTGGCTGCAGCTGGAGGGCCCCAAGGACAACGCCAGCAGAGCCAAGGTGAACGCCTTCTC A C KHNYN Ensembl:ENSG00000100441 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24430862..24432041 32194978 MeRIP-seq:(Medium) rs757406719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_881670,Human_RBP_ID_23118293 Human_Splice_Rec_1501941,Human_Splice_Rec_1501955,Human_Splice_Rec_1501969,Human_Splice_Rec_1501981 Human_miRNA_ID_2395682,Human_miRNA_ID_3069456 RMVar_hsa_circ_112558,RMVar_hsa_circ_165442 105081 RMVar_ID_105081 Human_SNP_ID_548248646 m1A Human chr14 - 24432075 24432074 24432075 CTCCCACGCCTCTTCCCCAGGCAACTCCTTCCACCCCCAATCCATCTCCCTGGGACCACCCTGTT CTCCCACGCCTCTTCCCCAGGCAACTCCTTCC_CCCCCAATCCATCTCCCTGGGACCACCCTGTT GT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:24432024..24432178;chr14:24431628..24432560 26863196 MeRIP-seq:(Medium) rs1566497862 Functional Loss DEL dbSNP153 33..33 33 - - - 105082 RMVar_ID_105082 Human_SNP_ID_548248652 m1A Human chr14 - 24432089 24432089 24432089 AGGGCCACTTCTCTCTCCCACGCCTCTTCCCCAGGCAACTCCTTCCACCCCCAATCCATCTCCCT AGGGCCACTTCTCTCTCCCACGCCTCTTCCCCTGGCAACTCCTTCCACCCCCAATCCATCTCCCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24431932..24432175 26863196 MeRIP-seq:(Medium) rs1378295183 Functional Loss SNV dbSNP153 33..33 33 - - - 105083 RMVar_ID_105083 Human_SNP_ID_548248734 m1A Human chr14 - 24432289 24432286 24432289 GAGAGGCATTCCCATTGTGGAGCCGCTGGAGGAGGGAGGCTCCTCGGGACTGAGCTGCCCTGTGA GAGAGGCATTCCCATTGTGGAGCCGCTGGAGG___GAGGCTCCTCGGGACTGAGCTGCCCTGTGA CCCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24432239..24432389 32194978 MeRIP-seq:(Medium) rs1289978638 Functional Loss DEL dbSNP153 33..35 33 - - - 105084 RMVar_ID_105084 Human_SNP_ID_548248788 m1A Human chr14 + 24432424 24432421 24432425 AGACCGGGGAGACGTGGGGGACAGGGGAGACAAGCAGCAGGGCATGGCACGGGGTCGGGGGCCTC AGACCGGGGAGACGTGGGGGACAGGGGAGA____CAGCAGGGCATGGCACGGGGTCGGGGGCCTC ACAAG A KHNYN Ensembl:ENSG00000100441 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24432376..24432491 26863196 MeRIP-seq:(Medium) rs1417256510 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_813947,Human_RBP_ID_1065691,Human_RBP_ID_3944470,Human_RBP_ID_5176771,Human_RBP_ID_8180874,Human_RBP_ID_9417745,Human_RBP_ID_17846906,Human_RBP_ID_22044486 Human_miRNA_ID_864395,Human_miRNA_ID_2381033,Human_miRNA_ID_2512426,Human_miRNA_ID_3024047,Human_miRNA_ID_3055249,Human_miRNA_ID_3090769 RMVar_hsa_circ_112558,RMVar_hsa_circ_165442 105085 RMVar_ID_105085 Human_SNP_ID_548249588 m1A Human chr14 + 24435565 24435565 24435565 TACTGGGGTGGTAATGGTGGGCCTGGGAAGGAAGGGAGCAGAGCACAAGGCTTTTCAAAGGAAAG TACTGGGGTGGTAATGGTGGGCCTGGGAAGGACGGGAGCAGAGCACAAGGCTTTTCAAAGGAAAG A C KHNYN Ensembl:ENSG00000100441 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:24435516..24435650 26863196 MeRIP-seq:(Medium) rs112092204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5176779,Human_RBP_ID_5315641,Human_RBP_ID_18936679,Human_RBP_ID_26778366 105086 RMVar_ID_105086 Human_SNP_ID_548249712 m1A Human chr14 + 24436152 24436152 24436152 TGACCAGTTCCGGGACCTGGCGGAGGAGTCTGAGAAGTGGATGGCAATCATCAGAGAACGGTGAG TGACCAGTTCCGGGACCTGGCGGAGGAGTCTGTGAAGTGGATGGCAATCATCAGAGAACGGTGAG A T KHNYN Ensembl:ENSG00000100441 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24436101..24436410 32194978 MeRIP-seq:(Medium) rs767887673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758125,Human_RBP_ID_881672,Human_RBP_ID_8794021,Human_RBP_ID_18980501 Human_Splice_Rec_1501948,Human_Splice_Rec_1501949,Human_Splice_Rec_1501962,Human_Splice_Rec_1501963,Human_Splice_Rec_1501976,Human_Splice_Rec_1501977,Human_Splice_Rec_1501986,Human_Splice_Rec_1501987,Human_Splice_Rec_1501991 105087 RMVar_ID_105087 Human_SNP_ID_548249794 m1A Human chr14 - 24436433 24436433 24436433 TCCAGGGTGGGGCCGTTTCGCCCCAGTGGGTCATCAGGTACCATGAAGAGGTTTCCCACAAAGGT TCCAGGGTGGGGCCGTTTCGCCCCAGTGGGTCGTCAGGTACCATGAAGAGGTTTCCCACAAAGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24436151..24437304 32194978 MeRIP-seq:(Medium) rs374951408 Functional Loss SNV dbSNP153 33..33 33 - - - 105088 RMVar_ID_105088 Human_SNP_ID_548249991 m1A Human chr14 - 24437134 24437134 24437134 GCCGGAGCCGCTCTGTTTCCCGGGTCTTCCGAATGCCACCACTACCTTTTTCCTCTTCTCTCCCC GCCGGAGCCGCTCTGTTTCCCGGGTCTTCCGAGTGCCACCACTACCTTTTTCCTCTTCTCTCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24437083..24437327 26863196 MeRIP-seq:(Medium) rs1264437936 Functional Loss SNV dbSNP153 33..33 33 - - - 105089 RMVar_ID_105089 Human_SNP_ID_548249992 m1A Human chr14 - 24437134 24437134 24437134 GCCGGAGCCGCTCTGTTTCCCGGGTCTTCCGAATGCCACCACTACCTTTTTCCTCTTCTCTCCCC GCCGGAGCCGCTCTGTTTCCCGGGTCTTCCGACTGCCACCACTACCTTTTTCCTCTTCTCTCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24437083..24437327 26863196 MeRIP-seq:(Medium) rs1264437936 Functional Loss SNV dbSNP153 33..33 33 - - - 105090 RMVar_ID_105090 Human_SNP_ID_548250430 m1A Human chr14 + 24439046 24439046 24439046 GAGACAGGCTGGTCAAAGAGGTGACAATGATTAAGAGATAACCCAGCGGTCCCTGAGAAGAGATT GAGACAGGCTGGTCAAAGAGGTGACAATGATTGAGAGATAACCCAGCGGTCCCTGAGAAGAGATT A G KHNYN Ensembl:ENSG00000100441 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24438996..24439096 32194978 MeRIP-seq:(Medium) rs903896782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4311966,Human_RBP_ID_17856850 105091 RMVar_ID_105091 Human_SNP_ID_548250593 m1A Human chr14 - 24439866 24439866 24439866 ATTAATCTTTTCAACTCCTTGTAAGATTTCCCAGTTTGGTTTCTCTACATGTCCTGCAGCTGCCC ATTAATCTTTTCAACTCCTTGTAAGATTTCCCTGTTTGGTTTCTCTACATGTCCTGCAGCTGCCC T A SDR39U1 Ensembl:ENSG00000100445 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1817226,Human_RBP_ID_9040295,Human_RBP_ID_17248467,Human_RBP_ID_21886686,Human_RBP_ID_26432489 Human_miRNA_ID_1797558 GWAS_ID_13717,GWAS_ID_13718,GWAS_ID_13719,GWAS_ID_13720,GWAS_ID_13721,GWAS_ID_13722,GWAS_ID_13723,GWAS_ID_13724,GWAS_ID_13725 105092 RMVar_ID_105092 Human_SNP_ID_548250594 m1A Human chr14 - 24439866 24439866 24439866 ATTAATCTTTTCAACTCCTTGTAAGATTTCCCAGTTTGGTTTCTCTACATGTCCTGCAGCTGCCC ATTAATCTTTTCAACTCCTTGTAAGATTTCCCGGTTTGGTTTCTCTACATGTCCTGCAGCTGCCC T C SDR39U1 Ensembl:ENSG00000100445 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1817226,Human_RBP_ID_9040295,Human_RBP_ID_17248467,Human_RBP_ID_21886686,Human_RBP_ID_26432489 Human_miRNA_ID_1797558 GWAS_ID_13717,GWAS_ID_13718,GWAS_ID_13719,GWAS_ID_13720,GWAS_ID_13721,GWAS_ID_13722,GWAS_ID_13723,GWAS_ID_13724,GWAS_ID_13725 105093 RMVar_ID_105093 Human_SNP_ID_548250707 m1A Human chr14 - 24440190 24440190 24440190 TGGTGCAAGCTGTCTTTGGGCGACAGCGTGCCATCATGCTGCTGGAGGGCCAGAAGGTGATCCCA TGGTGCAAGCTGTCTTTGGGCGACAGCGTGCCGTCATGCTGCTGGAGGGCCAGAAGGTGATCCCA T C SDR39U1 Ensembl:ENSG00000100445 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24440141..24440241 32194978 MeRIP-seq:(Medium) rs370095605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22045224,Human_RBP_ID_26756589,Human_RBP_ID_27430823 105094 RMVar_ID_105094 Human_SNP_ID_548251495 m1A Human chr14 - 24442416 24442415 24442416 CGGGACAGGCTTCATTGGGACAGCCCTAACCCAGCTGCTGAATGCCAGAGGCCACGAAGTGACGT CGGGACAGGCTTCATTGGGACAGCCCTAACCC_GCTGCTGAATGCCAGAGGCCACGAAGTGACGT CT C SDR39U1 Ensembl:ENSG00000100445 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24442183..24442450 26863196 MeRIP-seq:(Medium) rs777859318 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4308246,Human_RBP_ID_18979494,Human_RBP_ID_23118295,Human_RBP_ID_23617311,Human_RBP_ID_24558250,Human_RBP_ID_25123006 Human_Splice_Rec_1501995,Human_Splice_Rec_1502004,Human_Splice_Rec_1502005,Human_Splice_Rec_1502014,Human_Splice_Rec_1502020,Human_Splice_Rec_1502021,Human_Splice_Rec_1502033,Human_Splice_Rec_1502039,Human_Splice_Rec_1502050,Human_Splice_Rec_1502051,Human_Splice_Rec_1502061,Human_Splice_Rec_1502073,Human_Splice_Rec_1502077,Human_Splice_Rec_1502089,Human_Splice_Rec_1502098,Human_Splice_Rec_1502099,Human_Splice_Rec_1502110 105095 RMVar_ID_105095 Human_SNP_ID_548251551 m1A Human chr14 - 24442579 24442576 24442579 CCTGTGACCTGTGTCACCTCTGCATCGCGAGGAGGGGGATAAGTGGGGAGAAGCCTGGTGTCAGA CCTGTGACCTGTGTCACCTCTGCATCGCGAGG___GGGATAAGTGGGGAGAAGCCTGGTGTCAGA CCCT C SDR39U1 Ensembl:ENSG00000100445 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:24442556..24442742 26863196 MeRIP-seq:(Medium) rs1566508797 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1492280 105096 RMVar_ID_105096 Human_SNP_ID_548251599 m1A Human chr14 + 24442713 24442713 24442713 CCCGGAAGCGGATTCCCAGTCCTCAATCTCCGACTAAGCCCGCCCAGCACTCTCCCTTTCTGCCC CCCGGAAGCGGATTCCCAGTCCTCAATCTCCGGCTAAGCCCGCCCAGCACTCTCCCTTTCTGCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:24442637..24442742 26863196 MeRIP-seq:(Medium) rs763787420 Functional Loss SNV dbSNP153 33..33 33 - - - 105097 RMVar_ID_105097 Human_SNP_ID_548350786 m1A Human chr14 - 24811050 24811050 24811050 AAATTTAATAAACTGTATAAGTTAACTATAATATTTTATACTTTCTTTTTGGTGTCTTAAAAATT AAATTTAATAAACTGTATAAGTTAACTATAATGTTTTATACTTTCTTTTTGGTGTCTTAAAAATT T C STXBP6 Ensembl:ENSG00000168952 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3825590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26623578 105098 RMVar_ID_105098 Human_SNP_ID_548462004 m1A Human chr14 + 25267298 25267298 25267298 CTTCTCTGCGGTTCGTCCTTCACCTTGGCTTTATCTCCCTTAGCATCCCCTTCAGCCTTTCTCTT CTTCTCTGCGGTTCGTCCTTCACCTTGGCTTTCTCTCCCTTAGCATCCCCTTCAGCCTTTCTCTT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:25267256..25267339 26863196 MeRIP-seq:(Medium) rs551480725 Functional Loss SNV dbSNP153 33..33 33 - - - 105099 RMVar_ID_105099 Human_SNP_ID_548462005 m1A Human chr14 + 25267298 25267298 25267298 CTTCTCTGCGGTTCGTCCTTCACCTTGGCTTTATCTCCCTTAGCATCCCCTTCAGCCTTTCTCTT CTTCTCTGCGGTTCGTCCTTCACCTTGGCTTTGTCTCCCTTAGCATCCCCTTCAGCCTTTCTCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:25267256..25267339 26863196 MeRIP-seq:(Medium) rs551480725 Functional Loss SNV dbSNP153 33..33 33 - - - 105100 RMVar_ID_105100 Human_SNP_ID_548793976 m1A Human chr14 + 26597939 26597939 26597939 CGAGAGAGGAGCGAGCGGCAGAGGAGGGCAGGAGCCGGGAAGGAGCGCGGCGGTCCCCGCGCCGC CGAGAGAGGAGCGAGCGGCAGAGGAGGGCAGGGGCCGGGAAGGAGCGCGGCGGTCCCCGCGCCGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:26597888..26598116 26863196 MeRIP-seq:(Medium) rs971074111 Functional Loss SNV dbSNP153 33..33 33 - - - 105101 RMVar_ID_105101 Human_SNP_ID_549333182 m1A Human chr14 + 28767201 28767201 28767201 CTGCCGCCCGCGCCCCCCGCGCCCCGTTCGGCACCCACCGGTCGCCGCCGCCCGCCGCGCCGCTG CTGCCGCCCGCGCCCCCCGCGCCCCGTTCGGCCCCCACCGGTCGCCGCCGCCCGCCGCGCCGCTG A C FOXG1 Ensembl:ENSG00000176165 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:28767101..28767600 26863410 MeRIP-seq:(Medium) rs1038604992 Functional Loss SNV dbSNP153 33..33 33 - - - 105102 RMVar_ID_105102 Human_SNP_ID_143943853 m1A Human chr3 + 91891246 91891246 91891246 TACTCCCCGGTCTCGCTCATGTCTTCACCCCCAGCCCTCAGGGACTCTCCTGTGTGTCCCAGCTA TACTCCCCGGTCTCGCTCATGTCTTCACCCCCTGCCCTCAGGGACTCTCCTGTGTGTCCCAGCTA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:91891192..91891279 26863196 MeRIP-seq:(Medium) rs1295105704 Functional Loss SNV dbSNP153 33..33 33 - - - 105103 RMVar_ID_105103 Human_SNP_ID_144882056 m1A Human chr3 - 96617289 96617288 96617289 GTGCAAAGGTAGCATAATCACTTGTTCCTTAAATAGGGACTTGTATGAATGGCTCCACGAGGGTT GTGCAAAGGTAGCATAATCACTTGTTCCTTAA_TAGGGACTTGTATGAATGGCTCCACGAGGGTT AT A MTRNR2L12 Ensembl:ENSG00000269028 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1318057726 Functional Loss DEL dbSNP153 33..33 33 - - - 105104 RMVar_ID_105104 Human_SNP_ID_144882058 m1A Human chr3 - 96617289 96617289 96617289 GTGCAAAGGTAGCATAATCACTTGTTCCTTAAATAGGGACTTGTATGAATGGCTCCACGAGGGTT GTGCAAAGGTAGCATAATCACTTGTTCCTTAAGTAGGGACTTGTATGAATGGCTCCACGAGGGTT T C MTRNR2L12 Ensembl:ENSG00000269028 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1237508255 Functional Loss SNV dbSNP153 33..33 33 - - - 105105 RMVar_ID_105105 Human_SNP_ID_144882073 m1A Human chr3 + 96617320 96617320 96617320 ATTTAAGGAACAAGTGATTATGCTACCTTTGCACGGTTAGGGTACCGCGGCCGTTAAACATATGT ATTTAAGGAACAAGTGATTATGCTACCTTTGCCCGGTTAGGGTACCGCGGCCGTTAAACATATGT A C lnc-EPHA6-1,lnc-EPHA6-1:2 RNACentral:URS00008B4825,RNACentral:URS00008B49F0 lincRNA,lincRNA exon,exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:96617237..96617438 26863410 MeRIP-seq:(Medium) rs1169854900 Functional Loss SNV dbSNP153 33..33 33 - - - 105106 RMVar_ID_105106 Human_SNP_ID_144882074 m1A Human chr3 + 96617320 96617320 96617320 ATTTAAGGAACAAGTGATTATGCTACCTTTGCACGGTTAGGGTACCGCGGCCGTTAAACATATGT ATTTAAGGAACAAGTGATTATGCTACCTTTGCGCGGTTAGGGTACCGCGGCCGTTAAACATATGT A G lnc-EPHA6-1,lnc-EPHA6-1:2 RNACentral:URS00008B4825,RNACentral:URS00008B49F0 lincRNA,lincRNA exon,exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr3:96617237..96617438 26863410 MeRIP-seq:(Medium) rs1169854900 Functional Loss SNV dbSNP153 33..33 33 - - - 105107 RMVar_ID_105107 Human_SNP_ID_144882156 m1A Human chr3 + 96617490 96617490 96617490 CTTGTGGGCATGCCTGTGTTGGGTTAACAGTGAGGGTAATAATGGCTTGTTGGTTGATTGTAGAT CTTGTGGGCATGCCTGTGTTGGGTTAACAGTGTGGGTAATAATGGCTTGTTGGTTGATTGTAGAT A T lnc-EPHA6-1,lnc-EPHA6-1:2 RNACentral:URS00008B4825,RNACentral:URS00008B49F0 lincRNA,lincRNA exon,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:96617176..96617550;chr3:96617122..96617592;chr3:96617132..96617550;chr3:96617182..96617537;chr3:96617180..96617520;chr3:96617181..96617527 26863196 MeRIP-seq:(Medium) rs1377648442 Functional Loss SNV dbSNP153 33..33 33 - - - 105108 RMVar_ID_105108 Human_SNP_ID_145221826 m1A Human chr3 - 97972293 97972293 97972293 GATCCCGCGGGGCGCGCGCTGCTGCTTTAGGCACCCGGGCTCGGGTGCGGGTCTGGGAGACCTGT GATCCCGCGGGGCGCGCGCTGCTGCTTTAGGCCCCCGGGCTCGGGTGCGGGTCTGGGAGACCTGT T G RIOX2 Ensembl:ENSG00000170854 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:97972254..97972380 26863196 MeRIP-seq:(Medium) rs1055120665 Functional Loss SNV dbSNP153 33..33 33 - - - 105109 RMVar_ID_105109 Human_SNP_ID_145373697 m1A Human chr3 + 98519694 98519694 98519694 TCCAGGATTTGCCCCAGTCCCACTCCCAAAGTAGGTCTTTAACAGCATACCCAACTTCCCGTCTC TCCAGGATTTGCCCCAGTCCCACTCCCAAAGTCGGTCTTTAACAGCATACCCAACTTCCCGTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:98519656..98519825 26863196 MeRIP-seq:(Medium) rs1405062177 Functional Loss SNV dbSNP153 33..33 33 - - - 105110 RMVar_ID_105110 Human_SNP_ID_145374134 m1A Human chr3 + 98521413 98521413 98521413 AGCACACAAGCAATTACAAATGCTGTAGCAAAACGGTTATCCATTCTGGCATTCAGACTGCTCTG AGCACACAAGCAATTACAAATGCTGTAGCAAAGCGGTTATCCATTCTGGCATTCAGACTGCTCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:98521365..98521698 26863196 MeRIP-seq:(Medium) rs138604651 Functional Loss SNV dbSNP153 33..33 33 - - - 105111 RMVar_ID_105111 Human_SNP_ID_145374135 m1A Human chr3 + 98521413 98521413 98521413 AGCACACAAGCAATTACAAATGCTGTAGCAAAACGGTTATCCATTCTGGCATTCAGACTGCTCTG AGCACACAAGCAATTACAAATGCTGTAGCAAATCGGTTATCCATTCTGGCATTCAGACTGCTCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:98521365..98521698 26863196 MeRIP-seq:(Medium) rs138604651 Functional Loss SNV dbSNP153 33..33 33 - - - 105112 RMVar_ID_105112 Human_SNP_ID_145374146 m1A Human chr3 - 98521439 98521439 98521439 CTTATCTTCTTTCTTCAACTTCTAAACAGAGCAGTCTGAATGCCAGAATGGATAACCGTTTTGCT CTTATCTTCTTTCTTCAACTTCTAAACAGAGCGGTCTGAATGCCAGAATGGATAACCGTTTTGCT T C CLDND1,AC021660.3 Ensembl:ENSG00000080822,Ensembl:ENSG00000285635 Protein coding,Protein coding intron,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:98521379..98562360 26863410 MeRIP-seq:(Medium) rs1269644316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609354,Human_RBP_ID_785144,Human_RBP_ID_9146567,Human_RBP_ID_25762968 Human_Splice_Rec_457778,Human_Splice_Rec_457788,Human_Splice_Rec_457802,Human_Splice_Rec_457810,Human_Splice_Rec_457820,Human_Splice_Rec_457830,Human_Splice_Rec_457858,Human_Splice_Rec_457898,Human_Splice_Rec_457916,Human_Splice_Rec_457926,Human_Splice_Rec_457936,Human_Splice_Rec_457944,Human_Splice_Rec_457960,Human_Splice_Rec_457984,Human_Splice_Rec_457992,Human_Splice_Rec_457998,Human_Splice_Rec_458002,Human_Splice_Rec_458006,Human_Splice_Rec_458012 RMVar_hsa_circ_34061 105113 RMVar_ID_105113 Human_SNP_ID_145443987 m1A Human chr3 + 98797038 98797038 98797038 GCCGTATATGTATCAGACATATAAATGTAGTAAAAAAAAAAAAAAAAAAAATAGAAAACCTCTAC GCCGTATATGTATCAGACATATAAATGTAGTATAAAAAAAAAAAAAAAAAATAGAAAACCTCTAC A T ST3GAL6 Ensembl:ENSG00000064225 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98796938..98797038 32194978 MeRIP-seq:(Medium) rs1314972118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219938,RMVar_hsa_circ_219940 105114 RMVar_ID_105114 Human_SNP_ID_145444067 m1A Human chr3 + 98797288 98797288 98797288 AGAAAACACTTGCCCCTCTTAAAAAAAAAAAAACCCAAAACTAAACAACAACAACAAAAACCTCC AGAAAACACTTGCCCCTCTTAAAAAAAAAAAACCCCAAAACTAAACAACAACAACAAAAACCTCC A C ST3GAL6 Ensembl:ENSG00000064225 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98797237..98797437 32194978 MeRIP-seq:(Medium) rs963666300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219938,RMVar_hsa_circ_219940 105115 RMVar_ID_105115 Human_SNP_ID_145444880 m1A Human chr3 - 98800682 98800682 98800682 TGGTGGAAAGGAATGAAGCAGTTTCTTCCTGCAAAAGCAGTGGACCATGAGGAAACCCCAGTTCG TGGTGGAAAGGAATGAAGCAGTTTCTTCCTGCGAAAGCAGTGGACCATGAGGAAACCCCAGTTCG T C DCBLD2 Ensembl:ENSG00000057019 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98799681..98801392 32194978 MeRIP-seq:(Medium) rs759347951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_458480,Human_Splice_Rec_458510,Human_Splice_Rec_458514 Human_miRNA_ID_2359133,Human_miRNA_ID_2967757 RMVar_hsa_circ_58776,RMVar_hsa_circ_77478,RMVar_hsa_circ_122481,RMVar_hsa_circ_219941,RMVar_hsa_circ_219942,RMVar_hsa_circ_72528,RMVar_hsa_circ_266716 105116 RMVar_ID_105116 Human_SNP_ID_145444881 m1A Human chr3 - 98800682 98800682 98800682 TGGTGGAAAGGAATGAAGCAGTTTCTTCCTGCAAAAGCAGTGGACCATGAGGAAACCCCAGTTCG TGGTGGAAAGGAATGAAGCAGTTTCTTCCTGCCAAAGCAGTGGACCATGAGGAAACCCCAGTTCG T G DCBLD2 Ensembl:ENSG00000057019 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98799681..98801392 32194978 MeRIP-seq:(Medium) rs759347951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_458480,Human_Splice_Rec_458510,Human_Splice_Rec_458514 Human_miRNA_ID_2359133,Human_miRNA_ID_2967757 RMVar_hsa_circ_58776,RMVar_hsa_circ_77478,RMVar_hsa_circ_122481,RMVar_hsa_circ_219941,RMVar_hsa_circ_219942,RMVar_hsa_circ_72528,RMVar_hsa_circ_266716 105117 RMVar_ID_105117 Human_SNP_ID_145446464 m1A Human chr3 - 98806927 98806927 98806927 GAGTTAGGAAACCACTGAGGCCAGGCAGGCACATAACACACTGATTCTAGGAAAGGGAGAAGAGA GAGTTAGGAAACCACTGAGGCCAGGCAGGCACGTAACACACTGATTCTAGGAAAGGGAGAAGAGA T C DCBLD2 Ensembl:ENSG00000057019 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:98806832..98806987 26863196 MeRIP-seq:(Medium) rs1486909062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58776,RMVar_hsa_circ_77478,RMVar_hsa_circ_122481,RMVar_hsa_circ_219941,RMVar_hsa_circ_219942,RMVar_hsa_circ_72528,RMVar_hsa_circ_64701,RMVar_hsa_circ_100232,RMVar_hsa_circ_219943 105118 RMVar_ID_105118 Human_SNP_ID_145449167 m1A Human chr3 + 98819351 98819351 98819351 TCTCTTGCCCTGTGTGGTCAGTCCACTCCAGCACAGATGATGCTGTTATTTGAGGATCCGCGATC TCTCTTGCCCTGTGTGGTCAGTCCACTCCAGCGCAGATGATGCTGTTATTTGAGGATCCGCGATC A G ST3GAL6 Ensembl:ENSG00000064225 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98817886..98822720 32194978 MeRIP-seq:(Medium) rs1426315643 Functional Loss SNV dbSNP153 33..33 33 - - - 105119 RMVar_ID_105119 Human_SNP_ID_145471488 m1A Human chr3 - 98901466 98901466 98901466 GAGGAGTAGGTGAAAGCGGGGTGAGGGGCGGAAGGGTCCCGGCGCGGGGTGAGGCGAGGGCTGCC GAGGAGTAGGTGAAAGCGGGGTGAGGGGCGGAGGGGTCCCGGCGCGGGGTGAGGCGAGGGCTGCC T C DCBLD2 Ensembl:ENSG00000057019 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:98901170..98901655 26863196 MeRIP-seq:(Medium) rs1456880998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248091,Human_RBP_ID_834919,Human_RBP_ID_4755931,Human_RBP_ID_5530595,Human_RBP_ID_9435418,Human_RBP_ID_18464441,Human_RBP_ID_22456069,Human_RBP_ID_22608416,Human_RBP_ID_23258661,Human_RBP_ID_26790147 105120 RMVar_ID_105120 Human_SNP_ID_145666875 m1A Human chr3 + 99637910 99637910 99637910 CCTCTGGATGCTCAGAGGACAGGCAGCGCAGGAACTTCCTTGTCAAATAAGCCTTGCCTGGAGGG CCTCTGGATGCTCAGAGGACAGGCAGCGCAGGTACTTCCTTGTCAAATAAGCCTTGCCTGGAGGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:99637714..99637963 26863196 MeRIP-seq:(Medium) rs1481188836 Functional Loss SNV dbSNP153 33..33 33 - - - 105121 RMVar_ID_105121 Human_SNP_ID_145667094 m1A Human chr3 + 99638635 99638635 99638635 CCCTTCCCCGATCCTCTCCGTGGGAGCCAGCGAGCCTCTCTCCCTGATCTTACGTGCTCAAGGTA CCCTTCCCCGATCCTCTCCGTGGGAGCCAGCGGGCCTCTCTCCCTGATCTTACGTGCTCAAGGTA A G COL8A1 Ensembl:ENSG00000144810 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:99638486..99638700;chr3:99638484..99638711 26863196 MeRIP-seq:(Medium) rs180841675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_458593,Human_Splice_Rec_458597,Human_Splice_Rec_458603,Human_Splice_Rec_458611,Human_Splice_Rec_458617,Human_Splice_Rec_458625,Human_Splice_Rec_458631,Human_Splice_Rec_458637 105122 RMVar_ID_105122 Human_SNP_ID_145682774 m1A Human chr3 - 99703346 99703346 99703346 CCGGCTGCCAGGGCTGTTCTCCTGGCTCTGCAATTCACCGTCTGTGTGACTTCTCCGTTTCAGTT CCGGCTGCCAGGGCTGTTCTCCTGGCTCTGCAGTTCACCGTCTGTGTGACTTCTCCGTTTCAGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:99703344..99703427 26863196 MeRIP-seq:(Medium) rs1420526758 Functional Loss SNV dbSNP153 33..33 33 - - - 105123 RMVar_ID_105123 Human_SNP_ID_145704384 m1A Human chr3 + 99794561 99794561 99794561 CCAGGTGGGCCAGGGTTACCAGGGCAACCAGGACCAAAGGGTGATCGAGGACCCAAAGGACTACC CCAGGTGGGCCAGGGTTACCAGGGCAACCAGGCCCAAAGGGTGATCGAGGACCCAAAGGACTACC A C COL8A1 Ensembl:ENSG00000144810 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:99794511..99794675 26863196 MeRIP-seq:(Medium) rs767329177 Functional Loss SNV dbSNP153 33..33 33 - - - 105124 RMVar_ID_105124 Human_SNP_ID_145704385 m1A Human chr3 + 99794561 99794561 99794561 CCAGGTGGGCCAGGGTTACCAGGGCAACCAGGACCAAAGGGTGATCGAGGACCCAAAGGACTACC CCAGGTGGGCCAGGGTTACCAGGGCAACCAGGTCCAAAGGGTGATCGAGGACCCAAAGGACTACC A T COL8A1 Ensembl:ENSG00000144810 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:99794511..99794675 26863196 MeRIP-seq:(Medium) rs767329177 Functional Loss SNV dbSNP153 33..33 33 - - - 105125 RMVar_ID_105125 Human_SNP_ID_145704525 m1A Human chr3 - 99794999 99794999 99794999 TTCTCCCCTCTTGGTCCAAGAGCCCCAGGAACACCTCCCATGCCCCGGTCACCTTTGGGTCCTGG TTCTCCCCTCTTGGTCCAAGAGCCCCAGGAACGCCTCCCATGCCCCGGTCACCTTTGGGTCCTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:99794763..99795027 26863196 MeRIP-seq:(Medium) rs1241778338 Functional Loss SNV dbSNP153 33..33 33 - - - 105126 RMVar_ID_105126 Human_SNP_ID_145710233 m1A Human chr3 + 99817921 99817921 99817921 CTACGCCGGCCGCCTGGCTTTGAGACAACGTGATTCTCCGCAGCTGGTCGCCTACCCGTGATGTT CTACGCCGGCCGCCTGGCTTTGAGACAACGTGGTTCTCCGCAGCTGGTCGCCTACCCGTGATGTT A G CMSS1 Ensembl:ENSG00000184220 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:99817851..99818093 26863196 MeRIP-seq:(Medium) rs537897617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933254,Human_RBP_ID_1632860,Human_RBP_ID_1970809,Human_RBP_ID_4757361,Human_RBP_ID_9333787,Human_RBP_ID_9393865,Human_RBP_ID_14971196,Human_RBP_ID_18424022,Human_RBP_ID_18816164,Human_RBP_ID_23115861,Human_RBP_ID_26347057 RMVar_hsa_circ_92133,RMVar_hsa_circ_219969,RMVar_hsa_circ_79326,RMVar_hsa_circ_219968 105127 RMVar_ID_105127 Human_SNP_ID_145710240 m1A Human chr3 + 99817930 99817930 99817930 CCGCCTGGCTTTGAGACAACGTGATTCTCCGCAGCTGGTCGCCTACCCGTGATGTTCTGCCCACG CCGCCTGGCTTTGAGACAACGTGATTCTCCGCCGCTGGTCGCCTACCCGTGATGTTCTGCCCACG A C CMSS1 Ensembl:ENSG00000184220 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:99817851..99818084 26863196 MeRIP-seq:(Medium) rs768306918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933254,Human_RBP_ID_1632860,Human_RBP_ID_1970809,Human_RBP_ID_4757362,Human_RBP_ID_9333787,Human_RBP_ID_9393865,Human_RBP_ID_14971196,Human_RBP_ID_18424022,Human_RBP_ID_18816164,Human_RBP_ID_23115861,Human_RBP_ID_26347057 RMVar_hsa_circ_92133,RMVar_hsa_circ_219969,RMVar_hsa_circ_79326,RMVar_hsa_circ_219968 105128 RMVar_ID_105128 Human_SNP_ID_145714590 m1A Human chr3 - 99836108 99836108 99836108 ATCCAGCCTTAAATACCATTCTGATCACAGCAATTCTCCAGCCTCCCAGAAAACAGCACTTAAAA ATCCAGCCTTAAATACCATTCTGATCACAGCAGTTCTCCAGCCTCCCAGAAAACAGCACTTAAAA T C FILIP1L Ensembl:ENSG00000168386 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:99836106..99836213 26863196 MeRIP-seq:(Medium) rs1406123677 Functional Loss SNV dbSNP153 33..33 33 - - - 105129 RMVar_ID_105129 Human_SNP_ID_145739715 m1A Human chr3 + 99948647 99948643 99948647 GAGAGAGAGAGGAAGGAGGAGGAGGAGGGAGAAAGAAAGAGGGGAAGGGAAGGGAAAGAGGAAGA GAGAGAGAGAGGAAGGAGGAGGAGGAGGG____AGAAAGAGGGGAAGGGAAGGGAAAGAGGAAGA GAGAA G CMSS1 Ensembl:ENSG00000184220 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:99948645..99948716 26863196 MeRIP-seq:(Medium) rs538050686 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_25762253 RMVar_hsa_circ_92133,RMVar_hsa_circ_219968 105130 RMVar_ID_105130 Human_SNP_ID_145784992 m1A Human chr3 - 100146953 100146953 100146953 CCATCTGATGCTTCTAGAAAATATAAAGTTTGAAAATCAGAAAAGTCTCTCTCTCTCATTGCTAG CCATCTGATGCTTCTAGAAAATATAAAGTTTGTAAATCAGAAAAGTCTCTCTCTCTCATTGCTAG T A AC129803.1 Ensembl:ENSG00000287378 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:100146951..100147075 26863196 MeRIP-seq:(Medium) rs1430378904 Functional Loss SNV dbSNP153 33..33 33 - - - 105131 RMVar_ID_105131 Human_SNP_ID_145785027 m1A Human chr3 + 100147040 100147040 100147040 GTGATGCAGCAGGAGACAGTTCCAGTTCCTGTACCTTCAGAGAAAACCAAACAGGTGAGGGGTCA GTGATGCAGCAGGAGACAGTTCCAGTTCCTGTGCCTTCAGAGAAAACCAAACAGGTGAGGGGTCA A G CMSS1 Ensembl:ENSG00000184220 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:100146951..100147075 26863196 MeRIP-seq:(Medium) rs150607613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609686,Human_RBP_ID_18012664,Human_RBP_ID_26347058,Human_RBP_ID_27822382 Human_Splice_Rec_458650,Human_Splice_Rec_458651,Human_Splice_Rec_458654,Human_Splice_Rec_458655,Human_Splice_Rec_458674,Human_Splice_Rec_458675,Human_Splice_Rec_458696,Human_Splice_Rec_458697 RMVar_hsa_circ_66884,RMVar_hsa_circ_354591,RMVar_hsa_circ_354899 105132 RMVar_ID_105132 Human_SNP_ID_145828671 m1A Human chr3 + 100334795 100334795 100334795 CGCCGCAGGTGGTGCTTGTCTGCAGAGTCATGACCTGTAAGTGGCGCGGCCGCGCGCTGCAGCTC CGCCGCAGGTGGTGCTTGTCTGCAGAGTCATGGCCTGTAAGTGGCGCGGCCGCGCGCTGCAGCTC A G NIT2 Ensembl:ENSG00000114021 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:100334741..100334901 26863410 MeRIP-seq:(Medium) rs199753663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757363,Human_RBP_ID_19118072 Human_Splice_Rec_458975,Human_Splice_Rec_458991,Human_Splice_Rec_459001,Human_Splice_Rec_459019 RMVar_hsa_circ_219994,RMVar_hsa_circ_219996 105133 RMVar_ID_105133 Human_SNP_ID_145828690 m1A Human chr3 - 100334826 100334826 100334826 CGCTCCAAAGCCTCCCCCGCGGCCCGAACTCGAGCTGCAGCGCGCGGCCGCGCCACTTACAGGTC CGCTCCAAAGCCTCCCCCGCGGCCCGAACTCGTGCTGCAGCGCGCGGCCGCGCCACTTACAGGTC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:100334824..100334943 32194978 MeRIP-seq:(Medium) rs1038033415 Functional Loss SNV dbSNP153 33..33 33 - - - 105134 RMVar_ID_105134 Human_SNP_ID_145844506 m1A Human chr3 + 100400770 100400770 100400770 CGGCCTCTGGCCTCCCGGCGCCGTTGCTGCCGACTCCACAGGTATATGGCACCCGCGCCCAGCAG CGGCCTCTGGCCTCCCGGCGCCGTTGCTGCCGCCTCCACAGGTATATGGCACCCGCGCCCAGCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:100400720..100400814 26863196 MeRIP-seq:(Medium) rs757108241 Functional Loss SNV dbSNP153 33..33 33 - - - 105135 RMVar_ID_105135 Human_SNP_ID_145844541 m1A Human chr3 - 100400853 100400853 100400853 GGGTGGGCGGCGGCGGGACTGCGGGCCCGGGCACGGGGGGGCTGCCGCGATGGCAGCTGGCTCTG GGGTGGGCGGCGGCGGGACTGCGGGCCCGGGCGCGGGGGGGCTGCCGCGATGGCAGCTGGCTCTG T C TOMM70 Ensembl:ENSG00000154174 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:100386952..100401068 26863196 MeRIP-seq:(Medium) rs546607944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247438,Human_RBP_ID_783534,Human_RBP_ID_836508,Human_RBP_ID_4714924,Human_RBP_ID_5241542,Human_RBP_ID_5325281,Human_RBP_ID_8875584,Human_RBP_ID_9302423,Human_RBP_ID_22456071,Human_RBP_ID_27041485 RMVar_hsa_circ_96874,RMVar_hsa_circ_220008,RMVar_hsa_circ_119266,RMVar_hsa_circ_220015 105136 RMVar_ID_105136 Human_SNP_ID_145920315 m1A Human chr3 + 100709610 100709610 100709610 CTGCGAGCGAGGTGCGGCGGTCGCGAAGGGCAACCGAGGGGGCCGTGACCACCGCCTCCCCGCGA CTGCGAGCGAGGTGCGGCGGTCGCGAAGGGCAGCCGAGGGGGCCGTGACCACCGCCTCCCCGCGA A G TFG Ensembl:ENSG00000114354 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:100709378..100709833 26863196 MeRIP-seq:(Medium) rs1249206212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785227,Human_RBP_ID_4756623,Human_RBP_ID_17069264,Human_RBP_ID_26501668,Human_RBP_ID_26824854 105137 RMVar_ID_105137 Human_SNP_ID_145920316 m1A Human chr3 + 100709610 100709610 100709610 CTGCGAGCGAGGTGCGGCGGTCGCGAAGGGCAACCGAGGGGGCCGTGACCACCGCCTCCCCGCGA CTGCGAGCGAGGTGCGGCGGTCGCGAAGGGCATCCGAGGGGGCCGTGACCACCGCCTCCCCGCGA A T TFG Ensembl:ENSG00000114354 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:100709378..100709833 26863196 MeRIP-seq:(Medium) rs1249206212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785227,Human_RBP_ID_4756623,Human_RBP_ID_17069264,Human_RBP_ID_26501668,Human_RBP_ID_26824854 105138 RMVar_ID_105138 Human_SNP_ID_145921238 m1A Human chr3 + 100712897 100712897 100712897 TGAGGGGTATCAGAAAGGGTCAAGACAAAGGGAAAACTTGAAGTATGGGAATAGCAGGGGTGAGT TGAGGGGTATCAGAAAGGGTCAAGACAAAGGGCAAACTTGAAGTATGGGAATAGCAGGGGTGAGT A C TFG Ensembl:ENSG00000114354 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:100712891..100712976 26863196 MeRIP-seq:(Medium) rs981239639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7097269,Human_RBP_ID_14545203,Human_RBP_ID_22606282 105139 RMVar_ID_105139 Human_SNP_ID_146075789 m1A Human chr3 - 101361850 101361850 101361850 TTATGATTTATTCCTTGTTAGATGTCATCTGAATTATGCCCATATAATCCTGTCATGGAGAACAT TTATGATTTATTCCTTGTTAGATGTCATCTGAGTTATGCCCATATAATCCTGTCATGGAGAACAT T C SENP7 Ensembl:ENSG00000138468 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7616677 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9348877,Human_RBP_ID_26347065 Human_Splice_Rec_460152,Human_Splice_Rec_460192,Human_Splice_Rec_460236,Human_Splice_Rec_460280,Human_Splice_Rec_460336 GWAS_ID_13726,GWAS_ID_13727,GWAS_ID_13728,GWAS_ID_13729,GWAS_ID_13730,GWAS_ID_13731,GWAS_ID_13732,GWAS_ID_13733,GWAS_ID_13734,GWAS_ID_13735,GWAS_ID_13736,GWAS_ID_13737,GWAS_ID_13738,GWAS_ID_13739,GWAS_ID_13740,GWAS_ID_13741,GWAS_ID_13742,GWAS_ID_13743,GWAS_ID_13744,GWAS_ID_13745,GWAS_ID_13746,GWAS_ID_13747,GWAS_ID_13748,GWAS_ID_13749,GWAS_ID_13750,GWAS_ID_13751,GWAS_ID_13752,GWAS_ID_13753,GWAS_ID_13754,GWAS_ID_13755,GWAS_ID_13756,GWAS_ID_13757,GWAS_ID_13758,GWAS_ID_13759,GWAS_ID_13760,GWAS_ID_13761,GWAS_ID_13762,GWAS_ID_13763,GWAS_ID_13764,GWAS_ID_13765,GWAS_ID_13766,GWAS_ID_13767,GWAS_ID_13768,GWAS_ID_13769,GWAS_ID_13770,GWAS_ID_13771,GWAS_ID_13772,GWAS_ID_13773,GWAS_ID_13774,GWAS_ID_13775,GWAS_ID_13776,GWAS_ID_13777,GWAS_ID_13778,GWAS_ID_13779,GWAS_ID_13780,GWAS_ID_13781,GWAS_ID_13782,GWAS_ID_13783,GWAS_ID_13784,GWAS_ID_13785,GWAS_ID_13786,GWAS_ID_13787,GWAS_ID_13788,GWAS_ID_13789,GWAS_ID_13790,GWAS_ID_13791,GWAS_ID_13792,GWAS_ID_13793,GWAS_ID_13794,GWAS_ID_13795,GWAS_ID_13796,GWAS_ID_13797,GWAS_ID_13798,GWAS_ID_13799,GWAS_ID_13800,GWAS_ID_13801,GWAS_ID_13802,GWAS_ID_13803,GWAS_ID_13804,GWAS_ID_13805,GWAS_ID_13806,GWAS_ID_13807,GWAS_ID_13808,GWAS_ID_13809,GWAS_ID_13810,GWAS_ID_13811,GWAS_ID_13812,GWAS_ID_13813,GWAS_ID_13814,GWAS_ID_13815,GWAS_ID_13816,GWAS_ID_13817,GWAS_ID_13818,GWAS_ID_13819,GWAS_ID_13820,GWAS_ID_13821,GWAS_ID_13822,GWAS_ID_13823,GWAS_ID_13824,GWAS_ID_13825,GWAS_ID_13826,GWAS_ID_13827,GWAS_ID_13828,GWAS_ID_13829,GWAS_ID_13830,GWAS_ID_13831,GWAS_ID_13832,GWAS_ID_13833,GWAS_ID_13834,GWAS_ID_13835,GWAS_ID_13836,GWAS_ID_13837,GWAS_ID_13838,GWAS_ID_13839,GWAS_ID_13840,GWAS_ID_13841,GWAS_ID_13842,GWAS_ID_13843,GWAS_ID_13844,GWAS_ID_13845,GWAS_ID_13846,GWAS_ID_13847,GWAS_ID_13848,GWAS_ID_13849,GWAS_ID_13850,GWAS_ID_13851,GWAS_ID_13852,GWAS_ID_13853,GWAS_ID_13854,GWAS_ID_13855,GWAS_ID_13856,GWAS_ID_13857,GWAS_ID_13858,GWAS_ID_13859,GWAS_ID_13860,GWAS_ID_13861,GWAS_ID_13862,GWAS_ID_13863,GWAS_ID_13864,GWAS_ID_13865,GWAS_ID_13866,GWAS_ID_13867,GWAS_ID_13868,GWAS_ID_13869,GWAS_ID_13870,GWAS_ID_13871,GWAS_ID_13872,GWAS_ID_13873,GWAS_ID_13874,GWAS_ID_13875,GWAS_ID_13876,GWAS_ID_13877,GWAS_ID_13878,GWAS_ID_13879,GWAS_ID_13880,GWAS_ID_13881,GWAS_ID_13882,GWAS_ID_13883,GWAS_ID_13884,GWAS_ID_13885,GWAS_ID_13886,GWAS_ID_13887,GWAS_ID_13888,GWAS_ID_13889,GWAS_ID_13890,GWAS_ID_13891,GWAS_ID_13892,GWAS_ID_13893,GWAS_ID_13894,GWAS_ID_13895,GWAS_ID_13896,GWAS_ID_13897,GWAS_ID_13898,GWAS_ID_13899,GWAS_ID_13900,GWAS_ID_13901,GWAS_ID_13902,GWAS_ID_13903,GWAS_ID_13904,GWAS_ID_13905,GWAS_ID_13906,GWAS_ID_13907,GWAS_ID_13908,GWAS_ID_13909,GWAS_ID_13910,GWAS_ID_13911,GWAS_ID_13912,GWAS_ID_13913,GWAS_ID_13914,GWAS_ID_13915,GWAS_ID_13916,GWAS_ID_13917,GWAS_ID_13918,GWAS_ID_13919,GWAS_ID_13920,GWAS_ID_13921,GWAS_ID_13922,GWAS_ID_13923,GWAS_ID_13924,GWAS_ID_13925,GWAS_ID_13926,GWAS_ID_13927,GWAS_ID_13928,GWAS_ID_13929,GWAS_ID_13930,GWAS_ID_13931,GWAS_ID_13932,GWAS_ID_13933,GWAS_ID_13934,GWAS_ID_13935,GWAS_ID_13936,GWAS_ID_13937,GWAS_ID_13938,GWAS_ID_13939,GWAS_ID_13940,GWAS_ID_13941,GWAS_ID_13942,GWAS_ID_13943,GWAS_ID_13944,GWAS_ID_13945,GWAS_ID_13946,GWAS_ID_13947,GWAS_ID_13948,GWAS_ID_13949,GWAS_ID_13950,GWAS_ID_13951,GWAS_ID_13952,GWAS_ID_13953,GWAS_ID_13954,GWAS_ID_13955,GWAS_ID_13956,GWAS_ID_13957,GWAS_ID_13958,GWAS_ID_13959,GWAS_ID_13960,GWAS_ID_13961,GWAS_ID_13962,GWAS_ID_13963,GWAS_ID_13964,GWAS_ID_13965,GWAS_ID_13966,GWAS_ID_13967,GWAS_ID_13968,GWAS_ID_13969,GWAS_ID_13970,GWAS_ID_13971,GWAS_ID_13972,GWAS_ID_13973,GWAS_ID_13974,GWAS_ID_13975,GWAS_ID_13976,GWAS_ID_13977,GWAS_ID_13978,GWAS_ID_13979,GWAS_ID_13980,GWAS_ID_13981,GWAS_ID_13982,GWAS_ID_13983,GWAS_ID_13984,GWAS_ID_13985,GWAS_ID_13986,GWAS_ID_13987,GWAS_ID_13988,GWAS_ID_13989,GWAS_ID_13990,GWAS_ID_13991,GWAS_ID_13992 RMVar_hsa_circ_258,RMVar_hsa_circ_125297,RMVar_hsa_circ_220045,RMVar_hsa_circ_68576,RMVar_hsa_circ_12897,RMVar_hsa_circ_43436,RMVar_hsa_circ_334604,RMVar_hsa_circ_363248,RMVar_hsa_circ_220048,RMVar_hsa_circ_42476,RMVar_hsa_circ_306756,RMVar_hsa_circ_363657,RMVar_hsa_circ_11639,RMVar_hsa_circ_35031,RMVar_hsa_circ_14556,RMVar_hsa_circ_286579,RMVar_hsa_circ_5955,RMVar_hsa_circ_8059,RMVar_hsa_circ_11536,RMVar_hsa_circ_220050,RMVar_hsa_circ_220051,RMVar_hsa_circ_308699,RMVar_hsa_circ_38582,RMVar_hsa_circ_220052,RMVar_hsa_circ_1230,RMVar_hsa_circ_308456,RMVar_hsa_circ_323119,RMVar_hsa_circ_308384,RMVar_hsa_circ_220053,RMVar_hsa_circ_220054,RMVar_hsa_circ_220055 105140 RMVar_ID_105140 Human_SNP_ID_146098585 m1A Human chr3 - 101457475 101457475 101457475 AACAACCCTAAAGTTCAGGCATCTCTGGCAGCAAACACTTTCACCATTACAGGCCATGCCGAGAC AACAACCCTAAAGTTCAGGCATCTCTGGCAGCGAACACTTTCACCATTACAGGCCATGCCGAGAC T C AC110994.3,SENP7 Ensembl:ENSG00000282978,Ensembl:ENSG00000138468 Pseudogene,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879161338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363248,RMVar_hsa_circ_43423,RMVar_hsa_circ_220062,RMVar_hsa_circ_66458,RMVar_hsa_circ_311615,RMVar_hsa_circ_220060,RMVar_hsa_circ_294147 105141 RMVar_ID_105141 Human_SNP_ID_146123492 m1A Human chr3 - 101561949 101561949 101561949 CCCGCTGGCGCAAAGAACAGGGACCCTGGAGGACGAAGGACTCCGACGTACGGACGCCCAGGGAT CCCGCTGGCGCAAAGAACAGGGACCCTGGAGGCCGAAGGACTCCGACGTACGGACGCCCAGGGAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:101561898..101561995 26863196 MeRIP-seq:(Medium) rs906760028 Functional Loss SNV dbSNP153 33..33 33 - - - 105142 RMVar_ID_105142 Human_SNP_ID_146124237 m1A Human chr3 + 101565005 101565005 101565005 TAAGTGGAAAACTACCATGAAATCTAGTGTGCAAGAAGAATGTGTTTCAACAATCTCAAGCAGTA TAAGTGGAAAACTACCATGAAATCTAGTGTGCCAGAAGAATGTGTTTCAACAATCTCAAGCAGTA A C TRMT10C Ensembl:ENSG00000174173 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:101564955..101565056 32194978 MeRIP-seq:(Medium) rs758632984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1614821,Human_RBP_ID_22457401,Human_RBP_ID_23956270 105143 RMVar_ID_105143 Human_SNP_ID_146126796 m1A Human chr3 + 101574241 101574241 101574241 GGGGAAAATGGCGGACGGGAAGGCGGGAGACGAGAAGCCTGAAAAGTCGCAGCGAGCTGGAGCCG GGGGAAAATGGCGGACGGGAAGGCGGGAGACGTGAAGCCTGAAAAGTCGCAGCGAGCTGGAGCCG A T PCNP Ensembl:ENSG00000081154 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:101574163..101574771;chr3:101574176..101574853;chr3:101574176..101574357 26863196 MeRIP-seq:(Medium) rs769550715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247099,Human_RBP_ID_584077,Human_RBP_ID_782929,Human_RBP_ID_834726,Human_RBP_ID_933888,Human_RBP_ID_4715232,Human_RBP_ID_7098345,Human_RBP_ID_8235826,Human_RBP_ID_8554101,Human_RBP_ID_9334229,Human_RBP_ID_9393878,Human_RBP_ID_14550118,Human_RBP_ID_23026366,Human_RBP_ID_23115862,Human_RBP_ID_26347068,Human_RBP_ID_27822402 Human_Splice_Rec_460371,Human_Splice_Rec_460379,Human_Splice_Rec_460387,Human_Splice_Rec_460395,Human_Splice_Rec_460401,Human_Splice_Rec_460403 RMVar_hsa_circ_95215,RMVar_hsa_circ_220064 105144 RMVar_ID_105144 Human_SNP_ID_146126807 m1A Human chr3 - 101574255 101574255 101574255 GTGTTCACCTCCGGCGGCTCCAGCTCGCTGCGACTTTTCAGGCTTCTCGTCTCCCGCCTTCCCGT GTGTTCACCTCCGGCGGCTCCAGCTCGCTGCGGCTTTTCAGGCTTCTCGTCTCCCGCCTTCCCGT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr3:101574201..101574325 26863410 MeRIP-seq:(Medium) rs1346219571 Functional Loss SNV dbSNP153 33..33 33 - - - 105145 RMVar_ID_105145 Human_SNP_ID_146128338 m1A Human chr3 + 101579934 101579934 101579934 CGACCTCCCAACAAAGCCTACAAAGATCTCCAAGTTTGGATTTGCCATAGGTAGTCAGACGACAA CGACCTCCCAACAAAGCCTACAAAGATCTCCAGGTTTGGATTTGCCATAGGTAGTCAGACGACAA A G PCNP Ensembl:ENSG00000081154 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:101579826..101579975 32194978 MeRIP-seq:(Medium) rs759991840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584109,Human_RBP_ID_1614856,Human_RBP_ID_1945372,Human_RBP_ID_2729710,Human_RBP_ID_7098418,Human_RBP_ID_8554118,Human_RBP_ID_9393882,Human_RBP_ID_14550418,Human_RBP_ID_23956317 Human_Splice_Rec_460373,Human_Splice_Rec_460381,Human_Splice_Rec_460388,Human_Splice_Rec_460389,Human_Splice_Rec_460409 Human_miRNA_ID_1984071,Human_miRNA_ID_2614605,Human_miRNA_ID_2939710 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_106657,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220065,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 105146 RMVar_ID_105146 Human_SNP_ID_146153576 m1A Human chr3 - 101677223 101677223 101677223 ACCCGCATTCCTGACGTCACTGGATCGGCTCCATCAAGCCAGAAAACGAGAGTGCGCTCCAATCA ACCCGCATTCCTGACGTCACTGGATCGGCTCCGTCAAGCCAGAAAACGAGAGTGCGCTCCAATCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:101677172..101677273 32194978 MeRIP-seq:(Medium) rs755599161 Functional Loss SNV dbSNP153 33..33 33 - - - 105147 RMVar_ID_105147 Human_SNP_ID_146156125 m1A Human chr3 - 101685935 101685935 101685935 TATAGTTAAATAGTAATTCCTTTGCATTTGTCACTCTAGGTTTTCCAGTTTCTTAATGCGAAATG TATAGTTAAATAGTAATTCCTTTGCATTTGTCGCTCTAGGTTTTCCAGTTTCTTAATGCGAAATG T C RPL24 Ensembl:ENSG00000114391 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:101685926..101685950 26863196 MeRIP-seq:(Medium) rs1479128026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113809,RMVar_hsa_circ_89346,RMVar_hsa_circ_220097,RMVar_hsa_circ_220098,RMVar_hsa_circ_110100,RMVar_hsa_circ_220099 105148 RMVar_ID_105148 Human_SNP_ID_146156316 m1A Human chr3 - 101686478 101686478 101686478 GGAGGCGCTACGCCAGGACCGACGGGAAGGTAAAAAGCCGCGTCGGCTTCACCTACCTTCTTGTA GGAGGCGCTACGCCAGGACCGACGGGAAGGTAGAAAGCCGCGTCGGCTTCACCTACCTTCTTGTA T C RPL24 Ensembl:ENSG00000114391 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:101686476..101686500 32194978 MeRIP-seq:(Medium) rs1559993824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835265,Human_RBP_ID_22363947 Human_Splice_Rec_460450,Human_Splice_Rec_460460,Human_Splice_Rec_460470,Human_Splice_Rec_460478 RMVar_hsa_circ_113809,RMVar_hsa_circ_89346,RMVar_hsa_circ_220097,RMVar_hsa_circ_220098,RMVar_hsa_circ_110100,RMVar_hsa_circ_220099 105149 RMVar_ID_105149 Human_SNP_ID_146156400 m1A Human chr3 + 101686654 101686654 101686654 GAGTTCTGCCCGAGGATGTAAGCGGATTGGGAACCACGGGTCGTGCTTACTTCATGGCGACAGCT GAGTTCTGCCCGAGGATGTAAGCGGATTGGGAGCCACGGGTCGTGCTTACTTCATGGCGACAGCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr3:101686651..101686725 26863196 MeRIP-seq:(Medium) rs1466911657 Functional Loss SNV dbSNP153 33..33 33 - - - 105150 RMVar_ID_105150 Human_SNP_ID_146167187 m1A Human chr3 - 101726555 101726554 101726555 AAGAAACGGAAATGTTAGAAAACACAAATAAAATAAAACATGTACAACAGCTAAGCATAGGGCTG AAGAAACGGAAATGTTAGAAAACACAAATAAA_TAAAACATGTACAACAGCTAAGCATAGGGCTG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:101726554..101726621 26863196 MeRIP-seq:(Medium) rs1560006363 Functional Loss DEL dbSNP153 33..33 33 - - - 105151 RMVar_ID_105151 Human_SNP_ID_146175909 m1A Human chr3 + 101760024 101760021 101760025 TAAATAAGGAGGGAAAAACTGATGGTGCAGCAAAAAAAAAAAAAAAAAAAAAAAAGAGGAAGAGC TAAATAAGGAGGGAAAAACTGATGGTGCAG____AAAAAAAAAAAAAAAAAAAAAGAGGAAGAGC GCAAA G CEP97 Ensembl:ENSG00000182504 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:101760002..101760315 26863196 MeRIP-seq:(Medium) rs1324668014 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_9528,RMVar_hsa_circ_293018,RMVar_hsa_circ_220105,RMVar_hsa_circ_220108,RMVar_hsa_circ_325616 105152 RMVar_ID_105152 Human_SNP_ID_146180330 m1A Human chr3 - 101779284 101779284 101779284 CCCGCCCGCCCTTCGCTCTCCGGGGGCCAGGGATCCTGACGCCCCGGTCGGTCGCCGCAGCGCCA CCCGCCCGCCCTTCGCTCTCCGGGGGCCAGGGGTCCTGACGCCCCGGTCGGTCGCCGCAGCGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:101779234..101779323 26863196 MeRIP-seq:(Medium) rs573734351 Functional Loss SNV dbSNP153 33..33 33 - - - 105153 RMVar_ID_105153 Human_SNP_ID_146180437 m1A Human chr3 + 101779554 101779554 101779554 GAGGCCCGGGTCGAAGGCATAGGCAGAATTGGAGCCCTGGGTTGCCAAAGCGTCGCAGCTAAGAA GAGGCCCGGGTCGAAGGCATAGGCAGAATTGGTGCCCTGGGTTGCCAAAGCGTCGCAGCTAAGAA A T NXPE3 Ensembl:ENSG00000144815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:101779550..101779743 26863196 MeRIP-seq:(Medium) rs1473605234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9128839,Human_RBP_ID_14553472 RMVar_hsa_circ_80219,RMVar_hsa_circ_220109 105154 RMVar_ID_105154 Human_SNP_ID_146798183 m1A Human chr3 - 104160695 104160695 104160695 TTCGGCGCTCTCACCGCCACGACCCGGGTTCAATTCCCGGTCAGGGAACCAAGAAATGGTCTGGA TTCGGCGCTCTCACCGCCACGACCCGGGTTCAGTTCCCGGTCAGGGAACCAAGAAATGGTCTGGA T C tRNA-Glu-CTC-12-1 RNACentral:URS000074CBFD tRNA exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1469563206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270484,Human_RBP_ID_4716110,Human_RBP_ID_5209795,Human_RBP_ID_5424738,Human_RBP_ID_5446807,Human_RBP_ID_7100114,Human_RBP_ID_8265582,Human_RBP_ID_8866566,Human_RBP_ID_17026430,Human_RBP_ID_17667889,Human_RBP_ID_17702442,Human_RBP_ID_17990514,Human_RBP_ID_18209710,Human_RBP_ID_22423207,Human_RBP_ID_22821646,Human_RBP_ID_23026931,Human_RBP_ID_23134622,Human_RBP_ID_23312192,Human_RBP_ID_26750434,Human_RBP_ID_27042316,Human_RBP_ID_27311374 105155 RMVar_ID_105155 Human_SNP_ID_249150846 m1A Human chr5 - 122073287 122073287 122073287 AGTAGTGCTGAACTAAGCAGTTTGCATGTTTTATCATTGGAAAATGCGTGTCAGTTAAAATCTAT AGTAGTGCTGAACTAAGCAGTTTGCATGTTTTGTCATTGGAAAATGCGTGTCAGTTAAAATCTAT T C LOX Ensembl:ENSG00000113083 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:122073204..122073288 26863410 MeRIP-seq:(Medium) rs1161225452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2415,RMVar_hsa_circ_233993,RMVar_hsa_circ_103763 105156 RMVar_ID_105156 Human_SNP_ID_249152207 m1A Human chr5 + 122078101 122078101 122078101 GAGAAATCTTCAACCAAGGAGGCGAGCGGAGCACGGGTATCTCAGTCTCCACCAAGCAATGCCAA GAGAAATCTTCAACCAAGGAGGCGAGCGGAGCTCGGGTATCTCAGTCTCCACCAAGCAATGCCAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:122078052..122078305 26863196 MeRIP-seq:(Medium) rs1335573429 Functional Loss SNV dbSNP153 33..33 33 - - - 105157 RMVar_ID_105157 Human_SNP_ID_249334043 m1A Human chr5 + 122775144 122775144 122775144 CGAGAGGGAACCTCCTCCGCTGGGGGACGGGAAGCCCACCGACTTTGAGGATCTGGAGGACGGAG CGAGAGGGAACCTCCTCCGCTGGGGGACGGGAGGCCCACCGACTTTGAGGATCTGGAGGACGGAG A G SNX2 Ensembl:ENSG00000205302 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr5:122775076..122775248;chr5:122775095..122775192 26863196 MeRIP-seq:(Medium) rs1014883948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250997,Human_RBP_ID_629726,Human_RBP_ID_9398071,Human_RBP_ID_22511274,Human_RBP_ID_23050267 Human_Splice_Rec_684547,Human_Splice_Rec_684561,Human_Splice_Rec_684587,Human_Splice_Rec_684589,Human_Splice_Rec_684603 105158 RMVar_ID_105158 Human_SNP_ID_249334065 m1A Human chr5 - 122775200 122775188 122775200 CCCGCAGCGACGCGGTCTCACCTCTAGGGTGGAGACAGTGCTGGTGAACAGGTCCTCTCCGTCCT CCCGCAGCGACGCGGTCTCACCTCTAGGGTGG____________TGAACAGGTCCTCTCCGTCCT ACCAGCACTGTCT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:122775019..122775225 26863196 MeRIP-seq:(Medium) rs1273186625 Functional Loss DEL dbSNP153 33..44 33 - - - 105159 RMVar_ID_105159 Human_SNP_ID_249334069 m1A Human chr5 - 122775200 122775200 122775200 CCCGCAGCGACGCGGTCTCACCTCTAGGGTGGAGACAGTGCTGGTGAACAGGTCCTCTCCGTCCT CCCGCAGCGACGCGGTCTCACCTCTAGGGTGGCGACAGTGCTGGTGAACAGGTCCTCTCCGTCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:122775019..122775225 26863196 MeRIP-seq:(Medium) rs775575359 Functional Loss SNV dbSNP153 33..33 33 - - - 105160 RMVar_ID_105160 Human_SNP_ID_249339353 m1A Human chr5 + 122795217 122795217 122795217 TCTATTTCTGTAGTACATGGTGACAGAATTACAACAGGTAAACATGCCAATCCATTACCTATTAT TCTATTTCTGTAGTACATGGTGACAGAATTACGACAGGTAAACATGCCAATCCATTACCTATTAT A G SNX2 Ensembl:ENSG00000205302 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:122795207..122795300 26863196 MeRIP-seq:(Medium) rs890596559 Functional Loss SNV dbSNP153 33..33 33 - - - 105161 RMVar_ID_105161 Human_SNP_ID_249345109 m1A Human chr5 + 122817004 122817004 122817004 AACAAGGCTGCCGACGCTGTCAACAAAATGACAATCAAGATGAATGAATCGGATGCAGTAAGAGC AACAAGGCTGCCGACGCTGTCAACAAAATGACCATCAAGATGAATGAATCGGATGCAGTAAGAGC A C SNX2 Ensembl:ENSG00000205302 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:122815942..122817279 32194978 MeRIP-seq:(Medium) rs928442207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946386,Human_RBP_ID_1985218,Human_RBP_ID_3755183,Human_RBP_ID_9399307,Human_RBP_ID_24079017 Human_Splice_Rec_684560,Human_Splice_Rec_684576,Human_Splice_Rec_684577,Human_Splice_Rec_684628,Human_Splice_Rec_684629,Human_Splice_Rec_684652,Human_Splice_Rec_684653,Human_Splice_Rec_684666,Human_Splice_Rec_684667,Human_Splice_Rec_684669 Human_miRNA_ID_2239393,Human_miRNA_ID_2704409,Human_miRNA_ID_3016682 RMVar_hsa_circ_169,RMVar_hsa_circ_300931,RMVar_hsa_circ_338125,RMVar_hsa_circ_47807,RMVar_hsa_circ_234006,RMVar_hsa_circ_351169,RMVar_hsa_circ_17348,RMVar_hsa_circ_234014,RMVar_hsa_circ_359959,RMVar_hsa_circ_345749,RMVar_hsa_circ_15751,RMVar_hsa_circ_68760,RMVar_hsa_circ_352170 105162 RMVar_ID_105162 Human_SNP_ID_249356793 m1A Human chr5 + 122863284 122863284 122863284 AGGAGGTGAGGGGGTGAGTCATGAGGTTATCCAAGGGAAATGTCTTTTAGGCAGAAGGAGCAGTA AGGAGGTGAGGGGGTGAGTCATGAGGTTATCCGAGGGAAATGTCTTTTAGGCAGAAGGAGCAGTA A G SNX24 Ensembl:ENSG00000064652 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:122863274..122863405 26863196 MeRIP-seq:(Medium) rs1186190018 Functional Loss SNV dbSNP153 33..33 33 - - - 105163 RMVar_ID_105163 Human_SNP_ID_249395865 m1A Human chr5 - 123021033 123021033 123021033 AGTGATGGGCAGGCTGGGTGGGCTCAGGAAACAGCAAAGGGGCCAGATGAACAGAGCAGGGGAGG AGTGATGGGCAGGCTGGGTGGGCTCAGGAAACGGCAAAGGGGCCAGATGAACAGAGCAGGGGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:123020972..123021175 26863196 MeRIP-seq:(Medium) rs1254789918 Functional Loss SNV dbSNP153 33..33 33 - - - 105164 RMVar_ID_105164 Human_SNP_ID_249396106 m1A Human chr5 - 123021814 123021814 123021814 AATTCCAGGGCAGAAGAGAAAGCCAGTGTGTTAGGGCCTGGTGCAGAAAGGGGAGCGGGATAGGG AATTCCAGGGCAGAAGAGAAAGCCAGTGTGTTGGGGCCTGGTGCAGAAAGGGGAGCGGGATAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:123021720..123021955 26863196 MeRIP-seq:(Medium) rs1407984782 Functional Loss SNV dbSNP153 33..33 33 - - - 105165 RMVar_ID_105165 Human_SNP_ID_249399593 m1A Human chr5 - 123036662 123036662 123036662 TGTCCCAGAGCCTGTGTCGCGCCCGTGCCGGTAGCGCCCGTGCCGGTAGCGCCGCTGCCACCGCT TGTCCCAGAGCCTGTGTCGCGCCCGTGCCGGTGGCGCCCGTGCCGGTAGCGCCGCTGCCACCGCT T C PPIC Ensembl:ENSG00000168938 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:123036557..123036725 26863196 MeRIP-seq:(Medium) rs763525736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250903,Human_RBP_ID_4805758 105166 RMVar_ID_105166 Human_SNP_ID_249412580 m1A Human chr5 + 123090193 123090190 123090193 TCTTCAGCCGCCGCCGCCGCCCCCGCCCCCGGAGCGCGCTGAGCCTCCGCCGGACAGCCTGCGCC TCTTCAGCCGCCGCCGCCGCCCCCGCCCCC___GCGCGCTGAGCCTCCGCCGGACAGCCTGCGCC CGGA C PRDM6 Ensembl:ENSG00000061455 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:123090145..123090369 26863196 MeRIP-seq:(Medium) rs1156579295 Functional Loss DEL dbSNP153 31..33 33 - - - 105167 RMVar_ID_105167 Human_SNP_ID_249497417 m1A Human chr5 + 123423194 123423194 123423194 CGCCCGGCTCCTCTGCCTCGGGCCGCCAGCCCAGATCCTAACTGTGCCCCGACTCAAGGAAAAAG CGCCCGGCTCCTCTGCCTCGGGCCGCCAGCCCGGATCCTAACTGTGCCCCGACTCAAGGAAAAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:123423144..123423362 26863196 MeRIP-seq:(Medium) rs566768927 Functional Loss SNV dbSNP153 33..33 33 - - - 105168 RMVar_ID_105168 Human_SNP_ID_249519116 m1A Human chr5 - 123512315 123512315 123512315 CGCTGGTGCCTCCTACCGCCGCCGCTGGCCGGAGAGTCGCCGCCCGAGCCTCTGCTGTCGCCACC CGCTGGTGCCTCCTACCGCCGCCGCTGGCCGGGGAGTCGCCGCCCGAGCCTCTGCTGTCGCCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:123512198..123545443 26863196 MeRIP-seq:(Medium) rs923530964 Functional Loss SNV dbSNP153 33..33 33 - - - 105169 RMVar_ID_105169 Human_SNP_ID_249519119 m1A Human chr5 + 123512322 123512322 123512322 ACAGCAGAGGCTCGGGCGGCGACTCTCCGGCCAGCGGCGGCGGTAGGAGGCACCAGCGGCAGTGC ACAGCAGAGGCTCGGGCGGCGACTCTCCGGCCTGCGGCGGCGGTAGGAGGCACCAGCGGCAGTGC A T CSNK1G3 Ensembl:ENSG00000151292 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr5:123512188..123512425;chr5:123512222..123512583 26863196 MeRIP-seq:(Medium) rs1470778625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845314,Human_RBP_ID_18036928 105170 RMVar_ID_105170 Human_SNP_ID_249519307 m1A Human chr5 + 123512769 123512769 123512769 AGGACCATGGCGGGTGGCCCGGAGGCGTGGGCAGGAGGGGGCCGCGGTCGGAGGCTGAGGGCGCG AGGACCATGGCGGGTGGCCCGGAGGCGTGGGCCGGAGGGGGCCGCGGTCGGAGGCTGAGGGCGCG A C CSNK1G3 Ensembl:ENSG00000151292 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:123512745..123513020 26863196 MeRIP-seq:(Medium) rs1344273858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267108,Human_RBP_ID_3783293,Human_RBP_ID_5326529,Human_RBP_ID_8213184,Human_RBP_ID_9335290,Human_RBP_ID_9436565,Human_RBP_ID_18465368,Human_RBP_ID_26792108 105171 RMVar_ID_105171 Human_SNP_ID_250280392 m1A Human chr5 - 126423473 126423473 126423473 CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCATCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCTTCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC T A AC093535.1 Ensembl:ENSG00000250602 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126423426..126423652 26863196 MeRIP-seq:(Medium) rs996652926 Functional Loss SNV dbSNP153 33..33 33 - - - 105172 RMVar_ID_105172 Human_SNP_ID_250280393 m1A Human chr5 - 126423473 126423473 126423473 CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCATCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCGTCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC T C AC093535.1 Ensembl:ENSG00000250602 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126423426..126423652 26863196 MeRIP-seq:(Medium) rs996652926 Functional Loss SNV dbSNP153 33..33 33 - - - 105173 RMVar_ID_105173 Human_SNP_ID_250280394 m1A Human chr5 - 126423473 126423473 126423473 CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCATCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC CCGTGCCCTCCCCTGCACCCTCCGCCCAGCGCCTCCAGGCCGGGCCGCGCCAAGCTCCCGGGGCC T G AC093535.1 Ensembl:ENSG00000250602 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126423426..126423652 26863196 MeRIP-seq:(Medium) rs996652926 Functional Loss SNV dbSNP153 33..33 33 - - - 105174 RMVar_ID_105174 Human_SNP_ID_250280444 m1A Human chr5 - 126423586 126423586 126423586 TAGTTCAGTCATCGGGGCCGTGTCTGGAGGGCACCTTCAGACTTCCGCGCGCCTGGCTCTGCCCC TAGTTCAGTCATCGGGGCCGTGTCTGGAGGGCGCCTTCAGACTTCCGCGCGCCTGGCTCTGCCCC T C AC093535.1 Ensembl:ENSG00000250602 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:126423433..126423652 26863196 MeRIP-seq:(Medium) rs750190362 Functional Loss SNV dbSNP153 33..33 33 - - - 105175 RMVar_ID_105175 Human_SNP_ID_250285805 m1A Human chr5 + 126448278 126448277 126448278 GGTCAGTCCTTAGGACCTAGAGGGGGTTGGGGAAGTTGCCAGGTAGGAGGTGACCCCATCAAGAG GGTCAGTCCTTAGGACCTAGAGGGGGTTGGGG_AGTTGCCAGGTAGGAGGTGACCCCATCAAGAG GA G GRAMD2B Ensembl:ENSG00000155324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126448274..126448391 26863196 MeRIP-seq:(Medium) rs112284725 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_18558 105176 RMVar_ID_105176 Human_SNP_ID_250285806 m1A Human chr5 + 126448278 126448278 126448278 GGTCAGTCCTTAGGACCTAGAGGGGGTTGGGGAAGTTGCCAGGTAGGAGGTGACCCCATCAAGAG GGTCAGTCCTTAGGACCTAGAGGGGGTTGGGGGAGTTGCCAGGTAGGAGGTGACCCCATCAAGAG A G GRAMD2B Ensembl:ENSG00000155324 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126448274..126448391 26863196 MeRIP-seq:(Medium) rs11958374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18558 105177 RMVar_ID_105177 Human_SNP_ID_250309192 m1A Human chr5 - 126546369 126546369 126546369 AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGAGTCTGGCAGTGATGCCTGGAAACAGTACATGA AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGTGTCTGGCAGTGATGCCTGGAAACAGTACATGA T A ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126546326..126546418 26863196 MeRIP-seq:(Medium) rs80049945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250342,Human_RBP_ID_788310,Human_RBP_ID_945911,Human_RBP_ID_7375222,Human_RBP_ID_8600797 Human_Splice_Rec_685896,Human_Splice_Rec_685897,Human_Splice_Rec_685930,Human_Splice_Rec_685931,Human_Splice_Rec_685964,Human_Splice_Rec_685965,Human_Splice_Rec_686000,Human_Splice_Rec_686001,Human_Splice_Rec_686030,Human_Splice_Rec_686031,Human_Splice_Rec_686064,Human_Splice_Rec_686065,Human_Splice_Rec_686092,Human_Splice_Rec_686093,Human_Splice_Rec_686128,Human_Splice_Rec_686129,Human_Splice_Rec_686162,Human_Splice_Rec_686163,Human_Splice_Rec_686192,Human_Splice_Rec_686193,Human_Splice_Rec_686222,Human_Splice_Rec_686223,Human_Splice_Rec_686226,Human_Splice_Rec_686227,Human_Splice_Rec_686242,Human_Splice_Rec_686243,Human_Splice_Rec_686252,Human_Splice_Rec_686253,Human_Splice_Rec_686268,Human_Splice_Rec_686269,Human_Splice_Rec_686304,Human_Splice_Rec_686305,Human_Splice_Rec_686328,Human_Splice_Rec_686329,Human_Splice_Rec_686362,Human_Splice_Rec_686363,Human_Splice_Rec_686392,Human_Splice_Rec_686393,Human_Splice_Rec_686428 Clinvar_Rec_671 RMVar_hsa_circ_8437,RMVar_hsa_circ_344614,RMVar_hsa_circ_364955,RMVar_hsa_circ_265700,RMVar_hsa_circ_362992,RMVar_hsa_circ_71379,RMVar_hsa_circ_109291,RMVar_hsa_circ_46981,RMVar_hsa_circ_234067 105178 RMVar_ID_105178 Human_SNP_ID_250309193 m1A Human chr5 - 126546369 126546369 126546369 AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGAGTCTGGCAGTGATGCCTGGAAACAGTACATGA AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGGGTCTGGCAGTGATGCCTGGAAACAGTACATGA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126546326..126546418 26863196 MeRIP-seq:(Medium) rs80049945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250342,Human_RBP_ID_788310,Human_RBP_ID_945911,Human_RBP_ID_7375222,Human_RBP_ID_8600797 Human_Splice_Rec_685896,Human_Splice_Rec_685897,Human_Splice_Rec_685930,Human_Splice_Rec_685931,Human_Splice_Rec_685964,Human_Splice_Rec_685965,Human_Splice_Rec_686000,Human_Splice_Rec_686001,Human_Splice_Rec_686030,Human_Splice_Rec_686031,Human_Splice_Rec_686064,Human_Splice_Rec_686065,Human_Splice_Rec_686092,Human_Splice_Rec_686093,Human_Splice_Rec_686128,Human_Splice_Rec_686129,Human_Splice_Rec_686162,Human_Splice_Rec_686163,Human_Splice_Rec_686192,Human_Splice_Rec_686193,Human_Splice_Rec_686222,Human_Splice_Rec_686223,Human_Splice_Rec_686226,Human_Splice_Rec_686227,Human_Splice_Rec_686242,Human_Splice_Rec_686243,Human_Splice_Rec_686252,Human_Splice_Rec_686253,Human_Splice_Rec_686268,Human_Splice_Rec_686269,Human_Splice_Rec_686304,Human_Splice_Rec_686305,Human_Splice_Rec_686328,Human_Splice_Rec_686329,Human_Splice_Rec_686362,Human_Splice_Rec_686363,Human_Splice_Rec_686392,Human_Splice_Rec_686393,Human_Splice_Rec_686428 Clinvar_Rec_671 RMVar_hsa_circ_8437,RMVar_hsa_circ_344614,RMVar_hsa_circ_364955,RMVar_hsa_circ_265700,RMVar_hsa_circ_362992,RMVar_hsa_circ_71379,RMVar_hsa_circ_109291,RMVar_hsa_circ_46981,RMVar_hsa_circ_234067 105179 RMVar_ID_105179 Human_SNP_ID_250309194 m1A Human chr5 - 126546369 126546369 126546369 AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGAGTCTGGCAGTGATGCCTGGAAACAGTACATGA AGGAGGAGAAAAGCACACTGGTGGTGGCAGGGCGTCTGGCAGTGATGCCTGGAAACAGTACATGA T G ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126546326..126546418 26863196 MeRIP-seq:(Medium) rs80049945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250342,Human_RBP_ID_788310,Human_RBP_ID_945911,Human_RBP_ID_7375222,Human_RBP_ID_8600797 Human_Splice_Rec_685896,Human_Splice_Rec_685897,Human_Splice_Rec_685930,Human_Splice_Rec_685931,Human_Splice_Rec_685964,Human_Splice_Rec_685965,Human_Splice_Rec_686000,Human_Splice_Rec_686001,Human_Splice_Rec_686030,Human_Splice_Rec_686031,Human_Splice_Rec_686064,Human_Splice_Rec_686065,Human_Splice_Rec_686092,Human_Splice_Rec_686093,Human_Splice_Rec_686128,Human_Splice_Rec_686129,Human_Splice_Rec_686162,Human_Splice_Rec_686163,Human_Splice_Rec_686192,Human_Splice_Rec_686193,Human_Splice_Rec_686222,Human_Splice_Rec_686223,Human_Splice_Rec_686226,Human_Splice_Rec_686227,Human_Splice_Rec_686242,Human_Splice_Rec_686243,Human_Splice_Rec_686252,Human_Splice_Rec_686253,Human_Splice_Rec_686268,Human_Splice_Rec_686269,Human_Splice_Rec_686304,Human_Splice_Rec_686305,Human_Splice_Rec_686328,Human_Splice_Rec_686329,Human_Splice_Rec_686362,Human_Splice_Rec_686363,Human_Splice_Rec_686392,Human_Splice_Rec_686393,Human_Splice_Rec_686428 Clinvar_Rec_671 RMVar_hsa_circ_8437,RMVar_hsa_circ_344614,RMVar_hsa_circ_364955,RMVar_hsa_circ_265700,RMVar_hsa_circ_362992,RMVar_hsa_circ_71379,RMVar_hsa_circ_109291,RMVar_hsa_circ_46981,RMVar_hsa_circ_234067 105180 RMVar_ID_105180 Human_SNP_ID_250310171 m1A Human chr5 + 126549979 126549979 126549979 CAGCCCCACTTGTTGGAATGTTGACATTTACAATGCCACAGTCTGATCCTTTAGGTCTGTGTAAA CAGCCCCACTTGTTGGAATGTTGACATTTACAGTGCCACAGTCTGATCCTTTAGGTCTGTGTAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126549926..126550025 26863196 MeRIP-seq:(Medium) rs886059849 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_672,Clinvar_Rec_12682 105181 RMVar_ID_105181 Human_SNP_ID_250314980 m1A Human chr5 - 126568328 126568328 126568328 GCAGCACAGCAATGGCCAAAGATGAACGAGTGAACCTGCTGTCCTTCACTGGGAGCACTCAGGTG GCAGCACAGCAATGGCCAAAGATGAACGAGTGTACCTGCTGTCCTTCACTGGGAGCACTCAGGTG T A ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126568277..126568392 26863196 MeRIP-seq:(Medium) rs761387197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629969,Human_RBP_ID_25849249 Human_Splice_Rec_685880,Human_Splice_Rec_685881,Human_Splice_Rec_685914,Human_Splice_Rec_685915,Human_Splice_Rec_685948,Human_Splice_Rec_685949,Human_Splice_Rec_685984,Human_Splice_Rec_685985,Human_Splice_Rec_686018,Human_Splice_Rec_686019,Human_Splice_Rec_686048,Human_Splice_Rec_686049,Human_Splice_Rec_686076,Human_Splice_Rec_686077,Human_Splice_Rec_686112,Human_Splice_Rec_686113,Human_Splice_Rec_686146,Human_Splice_Rec_686147,Human_Splice_Rec_686176,Human_Splice_Rec_686177,Human_Splice_Rec_686210,Human_Splice_Rec_686211,Human_Splice_Rec_686288,Human_Splice_Rec_686289,Human_Splice_Rec_686376,Human_Splice_Rec_686377,Human_Splice_Rec_686410,Human_Splice_Rec_686411,Human_Splice_Rec_686444,Human_Splice_Rec_686445,Human_Splice_Rec_686468,Human_Splice_Rec_686469,Human_Splice_Rec_686494,Human_Splice_Rec_686495,Human_Splice_Rec_686510,Human_Splice_Rec_686511,Human_Splice_Rec_686532,Human_Splice_Rec_686533,Human_Splice_Rec_686542,Human_Splice_Rec_686543,Human_Splice_Rec_686558,Human_Splice_Rec_686572 RMVar_hsa_circ_14254,RMVar_hsa_circ_344614,RMVar_hsa_circ_265700,RMVar_hsa_circ_109291,RMVar_hsa_circ_37348,RMVar_hsa_circ_234067,RMVar_hsa_circ_329664,RMVar_hsa_circ_359337,RMVar_hsa_circ_15190,RMVar_hsa_circ_72210,RMVar_hsa_circ_234069,RMVar_hsa_circ_38717,RMVar_hsa_circ_29976,RMVar_hsa_circ_63356,RMVar_hsa_circ_268685,RMVar_hsa_circ_359173,RMVar_hsa_circ_16646,RMVar_hsa_circ_298420,RMVar_hsa_circ_58007,RMVar_hsa_circ_311644,RMVar_hsa_circ_234071,RMVar_hsa_circ_234072,RMVar_hsa_circ_331819,RMVar_hsa_circ_370455,RMVar_hsa_circ_329082,RMVar_hsa_circ_234074,RMVar_hsa_circ_23856,RMVar_hsa_circ_234073,RMVar_hsa_circ_321787,RMVar_hsa_circ_234078,RMVar_hsa_circ_277814,RMVar_hsa_circ_339886,RMVar_hsa_circ_350153,RMVar_hsa_circ_311131,RMVar_hsa_circ_97059,RMVar_hsa_circ_234076,RMVar_hsa_circ_234077,RMVar_hsa_circ_234075 105182 RMVar_ID_105182 Human_SNP_ID_250317729 m1A Human chr5 - 126579067 126579067 126579067 AGTAGGTATCCAAAATCCACAGGGTTATAAGCAAGGGGGTGACATCAGGGCAGAGATGGGAGGGC AGTAGGTATCCAAAATCCACAGGGTTATAAGCGAGGGGGTGACATCAGGGCAGAGATGGGAGGGC T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126579062..126579232 26863196 MeRIP-seq:(Medium) rs1408811714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344614,RMVar_hsa_circ_265700,RMVar_hsa_circ_37348,RMVar_hsa_circ_359337,RMVar_hsa_circ_15190,RMVar_hsa_circ_72210,RMVar_hsa_circ_29976,RMVar_hsa_circ_63356,RMVar_hsa_circ_16646,RMVar_hsa_circ_58007,RMVar_hsa_circ_370455,RMVar_hsa_circ_329082,RMVar_hsa_circ_234074,RMVar_hsa_circ_234073,RMVar_hsa_circ_234079,RMVar_hsa_circ_114609,RMVar_hsa_circ_350153,RMVar_hsa_circ_311131,RMVar_hsa_circ_97059,RMVar_hsa_circ_234076,RMVar_hsa_circ_346998,RMVar_hsa_circ_234075,RMVar_hsa_circ_301951,RMVar_hsa_circ_14822,RMVar_hsa_circ_234080,RMVar_hsa_circ_234081,RMVar_hsa_circ_288361,RMVar_hsa_circ_297396,RMVar_hsa_circ_234083,RMVar_hsa_circ_234084,RMVar_hsa_circ_292118,RMVar_hsa_circ_338467 105183 RMVar_ID_105183 Human_SNP_ID_250317750 m1A Human chr5 - 126579160 126579160 126579160 GGGTGCAGTGGTAGGGCAGATAGAGTGGAAAGAGAACCTCGGGAAGAGATTTTGTCTGACAAGGA GGGTGCAGTGGTAGGGCAGATAGAGTGGAAAGGGAACCTCGGGAAGAGATTTTGTCTGACAAGGA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:126579157..126579317 26863196 MeRIP-seq:(Medium) rs548256707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15279536 RMVar_hsa_circ_344614,RMVar_hsa_circ_265700,RMVar_hsa_circ_37348,RMVar_hsa_circ_359337,RMVar_hsa_circ_15190,RMVar_hsa_circ_72210,RMVar_hsa_circ_29976,RMVar_hsa_circ_63356,RMVar_hsa_circ_16646,RMVar_hsa_circ_58007,RMVar_hsa_circ_370455,RMVar_hsa_circ_329082,RMVar_hsa_circ_234074,RMVar_hsa_circ_234073,RMVar_hsa_circ_234079,RMVar_hsa_circ_114609,RMVar_hsa_circ_350153,RMVar_hsa_circ_311131,RMVar_hsa_circ_97059,RMVar_hsa_circ_234076,RMVar_hsa_circ_346998,RMVar_hsa_circ_234075,RMVar_hsa_circ_301951,RMVar_hsa_circ_14822,RMVar_hsa_circ_234080,RMVar_hsa_circ_234081,RMVar_hsa_circ_288361,RMVar_hsa_circ_297396,RMVar_hsa_circ_234083,RMVar_hsa_circ_234084,RMVar_hsa_circ_292118,RMVar_hsa_circ_338467 105184 RMVar_ID_105184 Human_SNP_ID_250318968 m1A Human chr5 - 126583980 126583980 126583980 ATTCCTGCTCCAAAACGAGGAGAAATAGTAAGACAGATTGGCGATGCCTTGCGGGAGAAGATCCA ATTCCTGCTCCAAAACGAGGAGAAATAGTAAGGCAGATTGGCGATGCCTTGCGGGAGAAGATCCA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126583910..126584063 26863196 MeRIP-seq:(Medium) rs762428797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76543,Human_RBP_ID_4806183,Human_RBP_ID_15279554 Human_Splice_Rec_685870,Human_Splice_Rec_685871,Human_Splice_Rec_685904,Human_Splice_Rec_685905,Human_Splice_Rec_685938,Human_Splice_Rec_685939,Human_Splice_Rec_685974,Human_Splice_Rec_685975,Human_Splice_Rec_686008,Human_Splice_Rec_686009,Human_Splice_Rec_686038,Human_Splice_Rec_686039,Human_Splice_Rec_686100,Human_Splice_Rec_686101,Human_Splice_Rec_686136,Human_Splice_Rec_686137,Human_Splice_Rec_686166,Human_Splice_Rec_686167,Human_Splice_Rec_686200,Human_Splice_Rec_686201,Human_Splice_Rec_686278,Human_Splice_Rec_686279,Human_Splice_Rec_686307,Human_Splice_Rec_686338,Human_Splice_Rec_686339,Human_Splice_Rec_686366,Human_Splice_Rec_686367,Human_Splice_Rec_686400,Human_Splice_Rec_686401,Human_Splice_Rec_686434,Human_Splice_Rec_686435,Human_Splice_Rec_686484,Human_Splice_Rec_686485,Human_Splice_Rec_686522,Human_Splice_Rec_686523,Human_Splice_Rec_686548,Human_Splice_Rec_686549,Human_Splice_Rec_686578,Human_Splice_Rec_686579,Human_Splice_Rec_686586,Human_Splice_Rec_686587,Human_Splice_Rec_686596,Human_Splice_Rec_686597,Human_Splice_Rec_686601,Human_Splice_Rec_686608,Human_Splice_Rec_686609 RMVar_hsa_circ_344614,RMVar_hsa_circ_265700,RMVar_hsa_circ_37348,RMVar_hsa_circ_359337,RMVar_hsa_circ_15190,RMVar_hsa_circ_72210,RMVar_hsa_circ_29976,RMVar_hsa_circ_16646,RMVar_hsa_circ_58007,RMVar_hsa_circ_370455,RMVar_hsa_circ_329082,RMVar_hsa_circ_234074,RMVar_hsa_circ_234073,RMVar_hsa_circ_234079,RMVar_hsa_circ_114609,RMVar_hsa_circ_350153,RMVar_hsa_circ_311131,RMVar_hsa_circ_346998,RMVar_hsa_circ_234075,RMVar_hsa_circ_301951,RMVar_hsa_circ_14822,RMVar_hsa_circ_234080,RMVar_hsa_circ_234081,RMVar_hsa_circ_288361,RMVar_hsa_circ_297396,RMVar_hsa_circ_234083,RMVar_hsa_circ_234084,RMVar_hsa_circ_292118,RMVar_hsa_circ_338467,RMVar_hsa_circ_234085,RMVar_hsa_circ_318307,RMVar_hsa_circ_374884,RMVar_hsa_circ_310944 105185 RMVar_ID_105185 Human_SNP_ID_250318980 m1A Human chr5 + 126584004 126584004 126584004 CCAATCTGTCTTACTATTTCTCCTCGTTTTGGAGCAGGAATCTAAGAAAAGAATGCAATTTTTGT CCAATCTGTCTTACTATTTCTCCTCGTTTTGGGGCAGGAATCTAAGAAAAGAATGCAATTTTTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:126583926..126584025 26863196 MeRIP-seq:(Medium) rs1325708741 Functional Loss SNV dbSNP153 33..33 33 - - - 105186 RMVar_ID_105186 Human_SNP_ID_250321238 m1A Human chr5 + 126592656 126592656 126592656 GTGATCTTTTCTGAATTCTAGAAACAAAGGCCATACTTACATCTGCCCAGATTTTCCATGCTTCT GTGATCTTTTCTGAATTCTAGAAACAAAGGCCGTACTTACATCTGCCCAGATTTTCCATGCTTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:126592651..126592700 26863196 MeRIP-seq:(Medium) rs774023027 Functional Loss SNV dbSNP153 33..33 33 - - - 105187 RMVar_ID_105187 Human_SNP_ID_250322057 m1A Human chr5 - 126595160 126595160 126595160 CGCCTTCCTCGCGCGCTGTGTGTGCACGCTGCAAAGACCAGCAAGCTCTCTGGACCTTGGAGCAG CGCCTTCCTCGCGCGCTGTGTGTGCACGCTGCGAAGACCAGCAAGCTCTCTGGACCTTGGAGCAG T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126594954..126595225 26863196 MeRIP-seq:(Medium) rs201566142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250344,Human_RBP_ID_945926,Human_RBP_ID_1318893,Human_RBP_ID_4846596,Human_RBP_ID_23120198,Human_RBP_ID_27073158 Clinvar_Rec_673 RMVar_hsa_circ_114609,RMVar_hsa_circ_234081 105188 RMVar_ID_105188 Human_SNP_ID_250322059 m1A Human chr5 + 126595163 126595163 126595163 CTCCAAGGTCCAGAGAGCTTGCTGGTCTTTGCAGCGTGCACACACAGCGCGCGAGGAAGGCGCCA CTCCAAGGTCCAGAGAGCTTGCTGGTCTTTGCGGCGTGCACACACAGCGCGCGAGGAAGGCGCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:126594953..126595200;chr5:126594946..126595175 26863196 MeRIP-seq:(Medium) rs779646478 Functional Loss SNV dbSNP153 33..33 33 - - - 105189 RMVar_ID_105189 Human_SNP_ID_250374397 m1A Human chr5 - 126777254 126777252 126777254 TCGCGAAATACCCTTTGTAAGAAAACACACACACCCACTCACACACGCACGCGGGAAAATGCAAG TCGCGAAATACCCTTTGTAAGAAAACACACAC__CCACTCACACACGCACGCGGGAAAATGCAAG GGT G LMNB1-DT,LMNB1-DT:2,RF00017-4490 RNACentral:URS0000D5B5C8,RNACentral:URS0000D5C962,RNACentral:URS0000941A94 lincRNA,lincRNA,SRP RNA intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:126777126..126777426 26863410 MeRIP-seq:(Medium) rs1452626478 Functional Loss DEL dbSNP153 33..34 33 - - - 105190 RMVar_ID_105190 Human_SNP_ID_250374398 m1A Human chr5 - 126777254 126777254 126777254 TCGCGAAATACCCTTTGTAAGAAAACACACACACCCACTCACACACGCACGCGGGAAAATGCAAG TCGCGAAATACCCTTTGTAAGAAAACACACACCCCCACTCACACACGCACGCGGGAAAATGCAAG T G LMNB1-DT,LMNB1-DT:2,RF00017-4490 RNACentral:URS0000D5B5C8,RNACentral:URS0000D5C962,RNACentral:URS0000941A94 lincRNA,lincRNA,SRP RNA intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:126777126..126777426 26863410 MeRIP-seq:(Medium) rs969090450 Functional Loss SNV dbSNP153 33..33 33 - - - 105191 RMVar_ID_105191 Human_SNP_ID_250374469 m1A Human chr5 - 126777492 126777492 126777492 GGGTCGCAGTCGCCATGGCGGGCGGCGGAGACAGCGGGGCGGCGAGGCCGCGAGCGGGACCGTGA GGGTCGCAGTCGCCATGGCGGGCGGCGGAGACTGCGGGGCGGCGAGGCCGCGAGCGGGACCGTGA T A LMNB1-DT,LMNB1-DT:2,RF00017-4490 RNACentral:URS0000D5B5C8,RNACentral:URS0000D5C962,RNACentral:URS0000941A94 lincRNA,lincRNA,SRP RNA intron,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr5:126777126..126777814;chr5:126777101..126777800 26863196,26863410 MeRIP-seq:(Medium) rs1561729760 Functional Loss SNV dbSNP153 33..33 33 - - - 105192 RMVar_ID_105192 Human_SNP_ID_250377691 m1A Human chr5 + 126787980 126787980 126787980 GATCATTCTGGCTATGCTGTGGAGGGAAAAAAAGAGGAGAGGTACAAACACTAGTAAGAACACTT GATCATTCTGGCTATGCTGTGGAGGGAAAAAATGAGGAGAGGTACAAACACTAGTAAGAACACTT A T LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:126787977..126788321 26863196 MeRIP-seq:(Medium) rs1419669150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15280257 RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_234092 105193 RMVar_ID_105193 Human_SNP_ID_250382407 m1A Human chr5 - 126804874 126804874 126804874 CCAAATCTCCCTCTAAACTTTTTTTGTCACCAAGTGCAGTAGCAAGAGCTGCATCTTTCGAATTC CCAAATCTCCCTCTAAACTTTTTTTGTCACCACGTGCAGTAGCAAGAGCTGCATCTTTCGAATTC T G RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:126804824..126805612 32194978 MeRIP-seq:(Medium) rs761744446 Functional Loss SNV dbSNP153 33..33 33 - - - 105194 RMVar_ID_105194 Human_SNP_ID_250383908 m1A Human chr5 + 126810343 126810343 126810343 GCTGTATAAGGAGGAGCTGGAGCAGACTTACCATGCCAAAGTGAGCTCTCTTCAGAAGATTCTTT GCTGTATAAGGAGGAGCTGGAGCAGACTTACCGTGCCAAAGTGAGCTCTCTTCAGAAGATTCTTT A G LMNB1 Ensembl:ENSG00000113368 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:126810293..126811805 32194978 MeRIP-seq:(Medium) rs1475181121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630002,Human_RBP_ID_1985500,Human_RBP_ID_7375675,Human_RBP_ID_8883574,Human_RBP_ID_9398085,Human_RBP_ID_15280920,Human_RBP_ID_22295075,Human_RBP_ID_26351158 Human_Splice_Rec_686659,Human_Splice_Rec_686681,Human_Splice_Rec_686701,Human_Splice_Rec_686725,Human_Splice_Rec_686735 Human_miRNA_ID_2492657,Human_miRNA_ID_2492658 RMVar_hsa_circ_77912,RMVar_hsa_circ_234094,RMVar_hsa_circ_62890,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_309463,RMVar_hsa_circ_331702,RMVar_hsa_circ_234092,RMVar_hsa_circ_317009,RMVar_hsa_circ_292305,RMVar_hsa_circ_275042,RMVar_hsa_circ_278490,RMVar_hsa_circ_269995,RMVar_hsa_circ_234096,RMVar_hsa_circ_234098,RMVar_hsa_circ_234099,RMVar_hsa_circ_234100,RMVar_hsa_circ_234097,RMVar_hsa_circ_234095,RMVar_hsa_circ_12255,RMVar_hsa_circ_52811,RMVar_hsa_circ_33052,RMVar_hsa_circ_274194,RMVar_hsa_circ_319195,RMVar_hsa_circ_347816,RMVar_hsa_circ_355681,RMVar_hsa_circ_336793,RMVar_hsa_circ_297079,RMVar_hsa_circ_234101,RMVar_hsa_circ_234102 105195 RMVar_ID_105195 Human_SNP_ID_250389246 m1A Human chr5 + 126832743 126832741 126832744 TACAGTCTTTAAAACAACCATACCTGAAGAAGAGGAGGAGGAGGAAGAAGCAGCTGGAGTGGTTG TACAGTCTTTAAAACAACCATACCTGAAGAA___GAGGAGGAGGAAGAAGCAGCTGGAGTGGTTG AGAG A LMNB1 Ensembl:ENSG00000113368 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:126832676..126832775 32194978 MeRIP-seq:(Medium) rs529151539 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_74374,Human_RBP_ID_946724,Human_RBP_ID_1985527,Human_RBP_ID_3755730,Human_RBP_ID_7375863,Human_RBP_ID_22458900,Human_RBP_ID_24386447,Human_RBP_ID_24502993,Human_RBP_ID_24548118 Human_Splice_Rec_686672,Human_Splice_Rec_686673,Human_Splice_Rec_686692,Human_Splice_Rec_686693,Human_Splice_Rec_686712,Human_Splice_Rec_686713 RMVar_hsa_circ_269995,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_301602 105196 RMVar_ID_105196 Human_SNP_ID_250392872 m1A Human chr5 + 126844640 126844640 126844640 ACACAGAGATAAGAGGTCGGGGTGTGGAAATAAGGGATTGGGGGTTCTTGCCCCGTAGAAAAGCG ACACAGAGATAAGAGGTCGGGGTGTGGAAATAGGGGATTGGGGGTTCTTGCCCCGTAGAAAAGCG A G KY945946 RNACentral:URS0000D02E8F lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:126844589..126844734 26863196 MeRIP-seq:(Medium) rs1041883426 Functional Loss SNV dbSNP153 33..33 33 - - - 105197 RMVar_ID_105197 Human_SNP_ID_250555680 m1A Human chr5 - 127517723 127517723 127517723 GCGTGGTCGCTGAAGAGTGTGGTATGATAGGGAGGTCGGGACGTAGAACTACAGCTTGGAGAAGA GCGTGGTCGCTGAAGAGTGTGGTATGATAGGGTGGTCGGGACGTAGAACTACAGCTTGGAGAAGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:127517672..127517817 26863196 MeRIP-seq:(Medium) rs1258764480 Functional Loss SNV dbSNP153 33..33 33 - - - 105198 RMVar_ID_105198 Human_SNP_ID_250555808 m1A Human chr5 - 127518123 127518123 127518123 AGGTCCGCCGGCGCTCCCGCCAGTCTCCCCTAAAGTCAGCGCCCTGGAAGGTGGGGCCAGAGCGC AGGTCCGCCGGCGCTCCCGCCAGTCTCCCCTACAGTCAGCGCCCTGGAAGGTGGGGCCAGAGCGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:127518116..127518221 32194978 MeRIP-seq:(Medium) rs943123164 Functional Loss SNV dbSNP153 33..33 33 - - - 105199 RMVar_ID_105199 Human_SNP_ID_250557446 m1A Human chr5 + 127524640 127524640 127524640 CCGCCCCTTCCTCCTGTGAGGCCTTCAGCACCATTACCTTTTGTGCCTCCTCCTGCAGTTCCTTC CCGCCCCTTCCTCCTGTGAGGCCTTCAGCACCTTTACCTTTTGTGCCTCCTCCTGCAGTTCCTTC A T PRRC1 Ensembl:ENSG00000164244 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:127524589..127524789 26863196 MeRIP-seq:(Medium) rs755088951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17415295,Human_RBP_ID_18956587,Human_RBP_ID_21112118 Human_miRNA_ID_2474696,Human_miRNA_ID_2960485 RMVar_hsa_circ_234114,RMVar_hsa_circ_309782,RMVar_hsa_circ_330224,RMVar_hsa_circ_332754,RMVar_hsa_circ_36541,RMVar_hsa_circ_293600,RMVar_hsa_circ_234115,RMVar_hsa_circ_234116,RMVar_hsa_circ_94672 105200 RMVar_ID_105200 Human_SNP_ID_250557447 m1A Human chr5 - 127524642 127524642 127524642 CAGAAGGAACTGCAGGAGGAGGCACAAAAGGTAATGGTGCTGAAGGCCTCACAGGAGGAAGGGGC CAGAAGGAACTGCAGGAGGAGGCACAAAAGGTGATGGTGCTGAAGGCCTCACAGGAGGAAGGGGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:127524594..127524786 26863196 MeRIP-seq:(Medium) rs924477699 Functional Loss SNV dbSNP153 33..33 33 - - - 105201 RMVar_ID_105201 Human_SNP_ID_250557562 m1A Human chr5 - 127524896 127524896 127524896 AGAATTACCTGTTCCTGAAGGTGCAGAAAATGATGGCATCAGGGGTGTCTGGGGAGCTCTCCCAG AGAATTACCTGTTCCTGAAGGTGCAGAAAATGGTGGCATCAGGGGTGTCTGGGGAGCTCTCCCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:127524655..127526751 32194978 MeRIP-seq:(Medium) rs1008879105 Functional Loss SNV dbSNP153 33..33 33 - - - 105202 RMVar_ID_105202 Human_SNP_ID_250564745 m1A Human chr5 + 127553001 127552999 127553001 CGTGGAAGCCTTTTCCCCTCAAATAATATATTATATCATTTTTGGACTTATATAAATGATAATTA CGTGGAAGCCTTTTCCCCTCAAATAATATAT__TATCATTTTTGGACTTATATAAATGATAATTA TTA T PRRC1 Ensembl:ENSG00000164244 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1220223112 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17526776,Human_RBP_ID_18037362,Human_RBP_ID_27733693 Human_miRNA_ID_1088615,Human_miRNA_ID_1119897,Human_miRNA_ID_1127029 105203 RMVar_ID_105203 Human_SNP_ID_250564747 m1A Human chr5 + 127553001 127553001 127553001 CGTGGAAGCCTTTTCCCCTCAAATAATATATTATATCATTTTTGGACTTATATAAATGATAATTA CGTGGAAGCCTTTTCCCCTCAAATAATATATTTTATCATTTTTGGACTTATATAAATGATAATTA A T PRRC1 Ensembl:ENSG00000164244 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs496004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17526776,Human_RBP_ID_18037362,Human_RBP_ID_27733693 Human_miRNA_ID_1088615,Human_miRNA_ID_1119897,Human_miRNA_ID_1127029 GWAS_ID_13993,GWAS_ID_13994,GWAS_ID_13995,GWAS_ID_13996,GWAS_ID_13997,GWAS_ID_13998,GWAS_ID_13999,GWAS_ID_14000,GWAS_ID_14001,GWAS_ID_14002,GWAS_ID_14003,GWAS_ID_14004,GWAS_ID_14005,GWAS_ID_14006,GWAS_ID_14007,GWAS_ID_14008,GWAS_ID_14009,GWAS_ID_14010,GWAS_ID_14011,GWAS_ID_14012,GWAS_ID_14013,GWAS_ID_14014,GWAS_ID_14015,GWAS_ID_14016,GWAS_ID_14017,GWAS_ID_14018,GWAS_ID_14019,GWAS_ID_14020,GWAS_ID_14021,GWAS_ID_14022,GWAS_ID_14023,GWAS_ID_14024,GWAS_ID_14025,GWAS_ID_14026,GWAS_ID_14027,GWAS_ID_14028,GWAS_ID_14029,GWAS_ID_14030,GWAS_ID_14031,GWAS_ID_14032,GWAS_ID_14033,GWAS_ID_14034,GWAS_ID_14035,GWAS_ID_14036,GWAS_ID_14037,GWAS_ID_14038,GWAS_ID_14039,GWAS_ID_14040,GWAS_ID_14041,GWAS_ID_14042,GWAS_ID_14043,GWAS_ID_14044,GWAS_ID_14045,GWAS_ID_14046,GWAS_ID_14047,GWAS_ID_14048,GWAS_ID_14049,GWAS_ID_14050,GWAS_ID_14051,GWAS_ID_14052,GWAS_ID_14053,GWAS_ID_14054,GWAS_ID_14055,GWAS_ID_14056,GWAS_ID_14057,GWAS_ID_14058,GWAS_ID_14059,GWAS_ID_14060,GWAS_ID_14061,GWAS_ID_14062,GWAS_ID_14063,GWAS_ID_14064,GWAS_ID_14065,GWAS_ID_14066,GWAS_ID_14067,GWAS_ID_14068 105204 RMVar_ID_105204 Human_SNP_ID_250679054 m1A Human chr5 - 128023062 128023062 128023062 AGATGATGGGAGTTCAGGGGCTAATTACAGCTATGGGGAAAAAGTAATGTATAAGCTGGAAGCCA AGATGATGGGAGTTCAGGGGCTAATTACAGCTGTGGGGAAAAAGTAATGTATAAGCTGGAAGCCA T C LINC01184 Ensembl:ENSG00000245937 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128023020..128023158 26863196 MeRIP-seq:(Medium) rs952663597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8215014 Human_miRNA_ID_2417081,Human_miRNA_ID_3174385 RMVar_hsa_circ_126759,RMVar_hsa_circ_234120 105205 RMVar_ID_105205 Human_SNP_ID_250679082 m1A Human chr5 + 128023195 128023195 128023195 TAGCTTCTACCTATTTCCATTTCTTTTTTTCCAGGTACTAAGTTATCTCTCCCTTATTTTATACA TAGCTTCTACCTATTTCCATTTCTTTTTTTCCTGGTACTAAGTTATCTCTCCCTTATTTTATACA A T lnc-CCDC192-3 RNACentral:URS00008BA120 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:128023057..128023203 26863196 MeRIP-seq:(Medium) rs763473879 Functional Loss SNV dbSNP153 33..33 33 - - - 105206 RMVar_ID_105206 Human_SNP_ID_250693402 m1A Human chr5 + 128084263 128084242 128084263 GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GCCGCTGCTGCG_____________________GCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GGCGGCGGCGGCGGCGGCGGCA G SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128084220..128084368 26863196 MeRIP-seq:(Medium) rs776231534 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_5531995 Human_miRNA_ID_2299801,Human_miRNA_ID_2303070,Human_miRNA_ID_2306334,Human_miRNA_ID_3010345 RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105207 RMVar_ID_105207 Human_SNP_ID_250693403 m1A Human chr5 + 128084263 128084245 128084263 GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GCCGCTGCTGCGGCG__________________GCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GGCGGCGGCGGCGGCGGCA G SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128084220..128084368 26863196 MeRIP-seq:(Medium) rs759381412 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_5531995 Human_miRNA_ID_2299801,Human_miRNA_ID_2303070,Human_miRNA_ID_2306334,Human_miRNA_ID_3010345 RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105208 RMVar_ID_105208 Human_SNP_ID_250693407 m1A Human chr5 + 128084263 128084248 128084263 GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GCCGCTGCTGCGGCGGCG_______________GCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GGCGGCGGCGGCGGCA G SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128084220..128084368 26863196 MeRIP-seq:(Medium) rs1238147587 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_5531995 Human_miRNA_ID_2299801,Human_miRNA_ID_2303070,Human_miRNA_ID_2306334,Human_miRNA_ID_3010345 RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105209 RMVar_ID_105209 Human_SNP_ID_250693412 m1A Human chr5 + 128084263 128084251 128084263 GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GCCGCTGCTGCGGCGGCGGCG____________GCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GGCGGCGGCGGCA G SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128084220..128084368 26863196 MeRIP-seq:(Medium) rs769579851 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_5531995 Human_miRNA_ID_2299801,Human_miRNA_ID_2303070,Human_miRNA_ID_2306334,Human_miRNA_ID_3010345 RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105210 RMVar_ID_105210 Human_SNP_ID_250693424 m1A Human chr5 + 128084263 128084263 128084263 GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA GCCGCTGCTGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGGTGCTGGGGCGGGGGCCAA A G SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:128084220..128084368 26863196 MeRIP-seq:(Medium) rs914390065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5531995 Human_miRNA_ID_2299801,Human_miRNA_ID_2303070,Human_miRNA_ID_2306334,Human_miRNA_ID_3010345 RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105211 RMVar_ID_105211 Human_SNP_ID_250693585 m1A Human chr5 + 128084511 128084511 128084511 GGACACGGTGCTGAGCGAGGGCAGCAGCCTGCACTCCGGCGGCGGCGGCGGCAGTGGGCACCACC GGACACGGTGCTGAGCGAGGGCAGCAGCCTGCCCTCCGGCGGCGGCGGCGGCAGTGGGCACCACC A C SLC12A2 Ensembl:ENSG00000064651 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:128084462..128084594 26863196 MeRIP-seq:(Medium) rs763077730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 105212 RMVar_ID_105212 Human_SNP_ID_250758491 m1A Human chr5 + 128338075 128338075 128338075 GTCACACTGAAAGCTGCCCTCAGTGTTCACACAGGTGCCACCCCTACAAAGGAGAGGGTTACGTT GTCACACTGAAAGCTGCCCTCAGTGTTCACACCGGTGCCACCCCTACAAAGGAGAGGGTTACGTT A C RF00017-071,RF00017-4567 RNACentral:URS00009310A4,RNACentral:URS000093B3AD SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:128338026..128338125 32194978 MeRIP-seq:(Medium) rs1554123060 Functional Loss SNV dbSNP153 33..33 33 - - - 105213 RMVar_ID_105213 Human_SNP_ID_250772052 m1A Human chr5 + 128393214 128393214 128393214 CCCCCAACGCCAGGAGAAAAGCCATTGCCTCCAGGGATGGGGATGAAGCCTGTCCCTCCTGGGCC CCCCCAACGCCAGGAGAAAAGCCATTGCCTCCGGGGATGGGGATGAAGCCTGTCCCTCCTGGGCC A G RF00017-071,RF00017-4567 RNACentral:URS00009310A4,RNACentral:URS000093B3AD SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:128393162..128393247 26863410 MeRIP-seq:(Medium) rs778468050 Functional Loss SNV dbSNP153 33..33 33 - - - 105214 RMVar_ID_105214 Human_SNP_ID_250808352 m1A Human chr5 - 128537912 128537912 128537912 AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGACGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGGCGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG T C FBN2 Ensembl:ENSG00000138829 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7732639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5476173 Clinvar_Rec_674 GWAS_ID_14069 RMVar_hsa_circ_99795,RMVar_hsa_circ_234187 105215 RMVar_ID_105215 Human_SNP_ID_250808353 m1A Human chr5 - 128537912 128537912 128537912 AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGACGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGCCGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG T G FBN2 Ensembl:ENSG00000138829 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7732639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5476173 Clinvar_Rec_674 GWAS_ID_14069 RMVar_hsa_circ_99795,RMVar_hsa_circ_234187 105216 RMVar_ID_105216 Human_SNP_ID_250808435 m1A Human chr5 - 128538178 128538178 128538178 TCTCTTGCTGGCCGCACGCCCCGGCCCCGCGCACCTCCGCCCGGCTCCGCAGCCGCTACCCGCGC TCTCTTGCTGGCCGCACGCCCCGGCCCCGCGCCCCTCCGCCCGGCTCCGCAGCCGCTACCCGCGC T G FBN2 Ensembl:ENSG00000138829 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:128538106..128538196 26863410 MeRIP-seq:(Medium) rs929995940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4807222 Human_miRNA_ID_2249961 RMVar_hsa_circ_99795,RMVar_hsa_circ_234187 105217 RMVar_ID_105217 Human_SNP_ID_250946525 m1A Human chr5 + 129094804 129094804 129094804 GGCTGCGGAGCCGGCGGTCCTTGCGCTCCCCAACAGCGGCGCCGGGGGCGCGGGGGCGCCGTCGG GGCTGCGGAGCCGGCGGTCCTTGCGCTCCCCAGCAGCGGCGCCGGGGGCGCGGGGGCGCCGTCGG A G ISOC1 Ensembl:ENSG00000066583 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:129094772..129094878 26863196 MeRIP-seq:(Medium) rs774564385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_283667,Human_RBP_ID_4845319,Human_RBP_ID_5426818,Human_RBP_ID_5476176,Human_RBP_ID_5508778,Human_RBP_ID_18037579,Human_RBP_ID_18448016 105218 RMVar_ID_105218 Human_SNP_ID_250946553 m1A Human chr5 - 129094849 129094849 129094849 AGGGTCGCGCGAAGACTGAGAAACAGAAGAGCACCGGGACTGTGCCCGACGGCGCCCCCGCGCCC AGGGTCGCGCGAAGACTGAGAAACAGAAGAGCCCCGGGACTGTGCCCGACGGCGCCCCCGCGCCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:129094751..129094925 26863410 MeRIP-seq:(Medium) rs1349401117 Functional Loss SNV dbSNP153 33..33 33 - - - 105219 RMVar_ID_105219 Human_SNP_ID_251214218 m1A Human chr5 - 130184513 130184513 130184513 AACTCCCATTCTATCACTTCATTTCTCTCCCGAGGCTGGAAGTGGTTGAAAGAAGGTATCACTCC AACTCCCATTCTATCACTTCATTTCTCTCCCGGGGCTGGAAGTGGTTGAAAGAAGGTATCACTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:130184434..130184512 32194978 MeRIP-seq:(Medium) rs1365251025 Functional Loss SNV dbSNP153 33..33 33 - - - 105220 RMVar_ID_105220 Human_SNP_ID_251453416 m1A Human chr5 - 131159372 131159370 131159372 AGTTAGGCAATTTCCAGTATGTTAAGTAACACACTTATTTTTGCCTGTGTATGGAGAGATTCAAG AGTTAGGCAATTTCCAGTATGTTAAGTAACAC__TTATTTTTGCCTGTGTATGGAGAGATTCAAG AGT A HINT1 Ensembl:ENSG00000169567 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:131159274..131159625 32194978 MeRIP-seq:(Medium) rs1470737661 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_283670,Human_RBP_ID_630396,Human_RBP_ID_1319014,Human_RBP_ID_1643857,Human_RBP_ID_1985822,Human_RBP_ID_2891660,Human_RBP_ID_3756438,Human_RBP_ID_4848893,Human_RBP_ID_7378796,Human_RBP_ID_8601476,Human_RBP_ID_9168960,Human_RBP_ID_10179218,Human_RBP_ID_17662693,Human_RBP_ID_17706872,Human_RBP_ID_18037794,Human_RBP_ID_18352610,Human_RBP_ID_18831531,Human_RBP_ID_22511328,Human_RBP_ID_22826993,Human_RBP_ID_23214247,Human_RBP_ID_24081074,Human_RBP_ID_24431648,Human_RBP_ID_24503103,Human_RBP_ID_25851090,Human_RBP_ID_27510986 105221 RMVar_ID_105221 Human_SNP_ID_251454948 m1A Human chr5 - 131165125 131165125 131165125 ACGATCTTTGGGAAGATCATCCGCAAGGAAATACCAGCCAAAATCATTTTTGAGGATGACCGGGT ACGATCTTTGGGAAGATCATCCGCAAGGAAATGCCAGCCAAAATCATTTTTGAGGATGACCGGGT T C HINT1 Ensembl:ENSG00000169567 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:131165101..131165125 26863196 MeRIP-seq:(Medium) rs1561538396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630409,Human_RBP_ID_1038552,Human_RBP_ID_1643871,Human_RBP_ID_4807348,Human_RBP_ID_9168967,Human_RBP_ID_17415307,Human_RBP_ID_18037806,Human_RBP_ID_22460157,Human_RBP_ID_27330777 Human_Splice_Rec_688095,Human_Splice_Rec_688099,Human_Splice_Rec_688107,Human_Splice_Rec_688113,Human_Splice_Rec_688121,Human_Splice_Rec_688129,Human_Splice_Rec_688133,Human_Splice_Rec_688135 Clinvar_Rec_675 105222 RMVar_ID_105222 Human_SNP_ID_251464155 m1A Human chr5 + 131202086 131202054 131202091 AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGTGTAAG AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTC GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTG LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs71591222 Functional Loss MNV dbSNP153 1..38 33 - - - Human_RBP_ID_165987 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234226,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 105223 RMVar_ID_105223 Human_SNP_ID_251464307 m1A Human chr5 + 131202611 131202611 131202611 ATAGCACACTGCAGCCTAGAATTTCTGACCTCAAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC ATAGCACACTGCAGCCTAGAATTTCTGACCTCCAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC A C LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs997305366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630464,Human_RBP_ID_17575722,Human_RBP_ID_26520643 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234226,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 105224 RMVar_ID_105224 Human_SNP_ID_251464308 m1A Human chr5 + 131202611 131202611 131202611 ATAGCACACTGCAGCCTAGAATTTCTGACCTCAAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC ATAGCACACTGCAGCCTAGAATTTCTGACCTCGAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs997305366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630464,Human_RBP_ID_17575722,Human_RBP_ID_26520643 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234226,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 105225 RMVar_ID_105225 Human_SNP_ID_251464317 m1A Human chr5 + 131202645 131202645 131202645 GCAATCATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGTGCATACCACCATAACCAGCTT GCAATCATCCTGCCTCAGCCTCCTAAGTAGCTGGGACTACAGGTGCATACCACCATAACCAGCTT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1240988824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520644 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234226,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 105226 RMVar_ID_105226 Human_SNP_ID_251478131 m1A Human chr5 + 131264102 131264102 131264102 CTGGGGAGCGCAGCTGCAGGCGTTGGGGCGGCAGGAGCCGCGGAGCCGGCGCTGAGAGGGGCTGC CTGGGGAGCGCAGCTGCAGGCGTTGGGGCGGCGGGAGCCGCGGAGCCGGCGCTGAGAGGGGCTGC A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:131264051..131316050 26863196 MeRIP-seq:(Medium) rs951389782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_789080,Human_RBP_ID_4845325,Human_RBP_ID_17157769,Human_RBP_ID_18037865,Human_RBP_ID_18425153,Human_RBP_ID_22614932,Human_RBP_ID_24081138 Human_Splice_Rec_688173,Human_Splice_Rec_688181,Human_Splice_Rec_688187,Human_Splice_Rec_688197,Human_Splice_Rec_688207 RMVar_hsa_circ_329116 105227 RMVar_ID_105227 Human_SNP_ID_251478164 m1A Human chr5 + 131264164 131264164 131264164 TGCGGCCGGAGCGGGCGGCTGAGACAAAGGCGACGGTGAGTGCAATGCCAGCCCCAGTCGCGCGT TGCGGCCGGAGCGGGCGGCTGAGACAAAGGCGTCGGTGAGTGCAATGCCAGCCCCAGTCGCGCGT A T CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:131264026..131264220;chr5:131264026..131316079;chr5:131264026..131316050 26863196 MeRIP-seq:(Medium) rs1403812207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1319023,Human_RBP_ID_4845913,Human_RBP_ID_17157769,Human_RBP_ID_18425153 Human_Splice_Rec_688173,Human_Splice_Rec_688181,Human_Splice_Rec_688187,Human_Splice_Rec_688197,Human_Splice_Rec_688207 RMVar_hsa_circ_329116 105228 RMVar_ID_105228 Human_SNP_ID_251558992 m1A Human chr5 - 131578215 131578215 131578215 AGGTAGAGAGTGACTGGAGAATAGGGGCAGGGATAAGAGTGAGTAGAAAAGTTAAAAAAAAGGAC AGGTAGAGAGTGACTGGAGAATAGGGGCAGGGGTAAGAGTGAGTAGAAAAGTTAAAAAAAAGGAC T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:131578168..131578252 26863196 MeRIP-seq:(Medium) rs934108814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839385 RMVar_hsa_circ_372094,RMVar_hsa_circ_234262,RMVar_hsa_circ_115166,RMVar_hsa_circ_234264,RMVar_hsa_circ_72930,RMVar_hsa_circ_234280,RMVar_hsa_circ_234278,RMVar_hsa_circ_124422,RMVar_hsa_circ_338175,RMVar_hsa_circ_234279,RMVar_hsa_circ_274553,RMVar_hsa_circ_292409,RMVar_hsa_circ_234281 105229 RMVar_ID_105229 Human_SNP_ID_251559064 m1A Human chr5 + 131578561 131578561 131578561 ACTCCGCATCTACTTATGGCACCTTTCTCCTTATGTCAATTCCATCCCCCCATATTTGGACCCCT ACTCCGCATCTACTTATGGCACCTTTCTCCTTTTGTCAATTCCATCCCCCCATATTTGGACCCCT A T RF00017-4673 RNACentral:URS000091B0E9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:131578510..131578638 26863196 MeRIP-seq:(Medium) rs1023242359 Functional Loss SNV dbSNP153 33..33 33 - - - 105230 RMVar_ID_105230 Human_SNP_ID_251559163 m1A Human chr5 - 131578950 131578950 131578950 TCCGCGGCTTCATTCTTGAAGTTAGTGAGACCAAGAACCCACCAATTTCGGACACAATGGGGCTG TCCGCGGCTTCATTCTTGAAGTTAGTGAGACCTAGAACCCACCAATTTCGGACACAATGGGGCTG T A AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:131578901..131579033 26863196 MeRIP-seq:(Medium) rs1160062733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372094,RMVar_hsa_circ_234262,RMVar_hsa_circ_115166,RMVar_hsa_circ_234264,RMVar_hsa_circ_72930,RMVar_hsa_circ_234280,RMVar_hsa_circ_234278,RMVar_hsa_circ_124422,RMVar_hsa_circ_338175,RMVar_hsa_circ_234279,RMVar_hsa_circ_274553,RMVar_hsa_circ_292409,RMVar_hsa_circ_234281 105231 RMVar_ID_105231 Human_SNP_ID_251559928 m1A Human chr5 - 131581472 131581472 131581472 GTTAAAAGCAGCATTTGTTGTGTAGAGTGATTAGTGATAGCCTGGATGCAGTTTCGTAGGAATTG GTTAAAAGCAGCATTTGTTGTGTAGAGTGATTGGTGATAGCCTGGATGCAGTTTCGTAGGAATTG T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:131581423..131581572 26863196 MeRIP-seq:(Medium) rs147622825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2892767,Human_RBP_ID_15289378,Human_RBP_ID_17159782 RMVar_hsa_circ_372094,RMVar_hsa_circ_234262,RMVar_hsa_circ_115166,RMVar_hsa_circ_234264,RMVar_hsa_circ_72930,RMVar_hsa_circ_234280,RMVar_hsa_circ_234278,RMVar_hsa_circ_124422,RMVar_hsa_circ_338175,RMVar_hsa_circ_234279,RMVar_hsa_circ_274553,RMVar_hsa_circ_292409,RMVar_hsa_circ_234281 105232 RMVar_ID_105232 Human_SNP_ID_251572850 m1A Human chr5 + 131635166 131635166 131635166 ACTTCGCGCCGTAACAAGGTCCGAACTCTAGCAAACAACCCTTCGCAACGCCCGCCTAAGGCCTC ACTTCGCGCCGTAACAAGGTCCGAACTCTAGCGAACAACCCTTCGCAACGCCCGCCTAAGGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:131634986..131635196 26863196 MeRIP-seq:(Medium) rs1344704932 Functional Loss SNV dbSNP153 33..33 33 - - - 105233 RMVar_ID_105233 Human_SNP_ID_251609678 m1A Human chr5 + 131789648 131789648 131789648 CAATTTCCTCCATCTTGACTAATATAATGGACACTTTTCTGTTTCTCATTTCACGAGACCTGTCA CAATTTCCTCCATCTTGACTAATATAATGGACGCTTTTCTGTTTCTCATTTCACGAGACCTGTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:131789643..131789855 26863196 MeRIP-seq:(Medium) rs1002091949 Functional Loss SNV dbSNP153 33..33 33 - - - 105234 RMVar_ID_105234 Human_SNP_ID_251709675 m1A Human chr5 - 132204125 132204125 132204125 TCTAGCTTGCACGAGCCACCGTTCGTGATCCCAAGACAGGAGTCCTCACTGTCGCCAGCTACCGG TCTAGCTTGCACGAGCCACCGTTCGTGATCCCGAGACAGGAGTCCTCACTGTCGCCAGCTACCGG T C P4HA2 Ensembl:ENSG00000072682 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132203790..132204124 32194978 MeRIP-seq:(Medium) rs147760022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968127,Human_RBP_ID_22459227,Human_RBP_ID_22771732 Human_Splice_Rec_690074,Human_Splice_Rec_690075,Human_Splice_Rec_690104,Human_Splice_Rec_690105,Human_Splice_Rec_690134,Human_Splice_Rec_690135,Human_Splice_Rec_690162,Human_Splice_Rec_690163,Human_Splice_Rec_690190,Human_Splice_Rec_690191,Human_Splice_Rec_690218,Human_Splice_Rec_690219 Human_miRNA_ID_1961715 RMVar_hsa_circ_2731,RMVar_hsa_circ_84873,RMVar_hsa_circ_234336,RMVar_hsa_circ_234337,RMVar_hsa_circ_36522,RMVar_hsa_circ_315077,RMVar_hsa_circ_120760,RMVar_hsa_circ_234338 105235 RMVar_ID_105235 Human_SNP_ID_251709676 m1A Human chr5 - 132204125 132204125 132204125 TCTAGCTTGCACGAGCCACCGTTCGTGATCCCAAGACAGGAGTCCTCACTGTCGCCAGCTACCGG TCTAGCTTGCACGAGCCACCGTTCGTGATCCCCAGACAGGAGTCCTCACTGTCGCCAGCTACCGG T G P4HA2 Ensembl:ENSG00000072682 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132203790..132204124 32194978 MeRIP-seq:(Medium) rs147760022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3968127,Human_RBP_ID_22459227,Human_RBP_ID_22771732 Human_Splice_Rec_690074,Human_Splice_Rec_690075,Human_Splice_Rec_690104,Human_Splice_Rec_690105,Human_Splice_Rec_690134,Human_Splice_Rec_690135,Human_Splice_Rec_690162,Human_Splice_Rec_690163,Human_Splice_Rec_690190,Human_Splice_Rec_690191,Human_Splice_Rec_690218,Human_Splice_Rec_690219 Human_miRNA_ID_1961715 RMVar_hsa_circ_2731,RMVar_hsa_circ_84873,RMVar_hsa_circ_234336,RMVar_hsa_circ_234337,RMVar_hsa_circ_36522,RMVar_hsa_circ_315077,RMVar_hsa_circ_120760,RMVar_hsa_circ_234338 105236 RMVar_ID_105236 Human_SNP_ID_251711028 m1A Human chr5 - 132209327 132209327 132209327 TTTCCTTCTCATTCCTTGCATTTTCTAGACCCAAGCCACGAACGAGCTGGAGGGAATCTGCGGTA TTTCCTTCTCATTCCTTGCATTTTCTAGACCCGAGCCACGAACGAGCTGGAGGGAATCTGCGGTA T C P4HA2 Ensembl:ENSG00000072682 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132209276..132209350 32194978 MeRIP-seq:(Medium) rs768503731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22459231,Human_RBP_ID_22771440,Human_RBP_ID_27825714 Human_Splice_Rec_690070,Human_Splice_Rec_690100,Human_Splice_Rec_690130,Human_Splice_Rec_690158,Human_Splice_Rec_690186,Human_Splice_Rec_690214 RMVar_hsa_circ_2731,RMVar_hsa_circ_84873,RMVar_hsa_circ_234336,RMVar_hsa_circ_1013,RMVar_hsa_circ_36522,RMVar_hsa_circ_310936 105237 RMVar_ID_105237 Human_SNP_ID_251714221 m1A Human chr5 - 132222445 132222445 132222445 GAGGCCAGTGTAGTGGGGGCCAGGATGCCTGTAGGGGAAGTTAGGGGTGGCTCAGATCAGGGTGA GAGGCCAGTGTAGTGGGGGCCAGGATGCCTGTGGGGGAAGTTAGGGGTGGCTCAGATCAGGGTGA T C P4HA2 Ensembl:ENSG00000072682 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:132222416..132222510 26863196 MeRIP-seq:(Medium) rs1452422278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90796,RMVar_hsa_circ_234340 105238 RMVar_ID_105238 Human_SNP_ID_251715407 m1A Human chr5 + 132227393 132227393 132227393 GAACGGGCTTAGCCAATATGAAGAGGCCCCTCAGGGCCAGGCGGACGCCGCGCCCCCGCTCCCAA GAACGGGCTTAGCCAATATGAAGAGGCCCCTCCGGGCCAGGCGGACGCCGCGCCCCCGCTCCCAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:132227366..132227787 26863196 MeRIP-seq:(Medium) rs969871531 Functional Loss SNV dbSNP153 33..33 33 - - - 105239 RMVar_ID_105239 Human_SNP_ID_251723845 m1A Human chr5 + 132262673 132262673 132262673 CCTGTGCCCAGGAGACCTGATCCAGGCCATCAATGGTGAGAGCACAGAGCTCATGACACACCTGG CCTGTGCCCAGGAGACCTGATCCAGGCCATCAGTGGTGAGAGCACAGAGCTCATGACACACCTGG A G PDLIM4 Ensembl:ENSG00000131435 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132262601..132262675 32194978 MeRIP-seq:(Medium) rs751349427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1210452,Human_RBP_ID_4845921,Human_RBP_ID_26826492 Human_Splice_Rec_690336,Human_Splice_Rec_690337,Human_Splice_Rec_690340,Human_Splice_Rec_690341,Human_Splice_Rec_690354,Human_Splice_Rec_690355,Human_Splice_Rec_690364,Human_Splice_Rec_690365 RMVar_hsa_circ_50851 105240 RMVar_ID_105240 Human_SNP_ID_251726259 m1A Human chr5 - 132272142 132272142 132272142 GGCGGCTTCACGCGCGCCTTGGCGTGGCTCTCACAGTAGAGCCGCTCGTCCAGAAAGAAGTAACC GGCGGCTTCACGCGCGCCTTGGCGTGGCTCTCGCAGTAGAGCCGCTCGTCCAGAAAGAAGTAACC T C P4HA2 Ensembl:ENSG00000072682 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:132271776..132272300 32194978 MeRIP-seq:(Medium) rs369789349 Functional Loss SNV dbSNP153 33..33 33 - - - 105241 RMVar_ID_105241 Human_SNP_ID_251746985 m1A Human chr5 - 132363560 132363560 132363560 TGTGCTCGGGGTGACTAAGTAACGGAGAGAAGACCAGCGTGACTAGAACATAGTGATCAAAGTGA TGTGCTCGGGGTGACTAAGTAACGGAGAGAAGGCCAGCGTGACTAGAACATAGTGATCAAAGTGA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132363509..132363653 26863196 MeRIP-seq:(Medium) rs1561556897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090110,Human_RBP_ID_15292515,Human_RBP_ID_24081883 105242 RMVar_ID_105242 Human_SNP_ID_251748513 m1A Human chr5 - 132369963 132369962 132369964 GTCACCTCGTCGTAGTCCCGCATGCCGCCCTCAGAGGCCCACAGAGCGCGGCCTGGGGTCGGGGA GTCACCTCGTCGTAGTCCCGCATGCCGCCCT__GAGGCCCACAGAGCGCGGCCTGGGGTCGGGGA CTG C MIR3936HG Ensembl:ENSG00000233006 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132369917..132369997 26863196 MeRIP-seq:(Medium) rs1362065170 Functional Loss DEL dbSNP153 32..33 33 - - - 105243 RMVar_ID_105243 Human_SNP_ID_251751234 m1A Human chr5 + 132381004 132381004 132381004 ATGCTTAGAGGCCACCTGAGTGGACATGGGAGATTCCTTCTCACGGAGCTAAGTGACAGCTGCGG ATGCTTAGAGGCCACCTGAGTGGACATGGGAGTTTCCTTCTCACGGAGCTAAGTGACAGCTGCGG A T SLC22A5 Ensembl:ENSG00000197375 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132380998..132381070 26863196 MeRIP-seq:(Medium) rs1472193858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5396149,Human_RBP_ID_9436722,Human_RBP_ID_15292607,Human_RBP_ID_21990267,Human_RBP_ID_24081897 RMVar_hsa_circ_234343,RMVar_hsa_circ_114990 105244 RMVar_ID_105244 Human_SNP_ID_251752297 m1A Human chr5 + 132385985 132385984 132385986 GAGGCCATTCCAGACCAAGAGGGGAACACTGCAGAGGTGCTAAGGTGGGAATCACCCCTTGCAGG GAGGCCATTCCAGACCAAGAGGGGAACACTGC__AGGTGCTAAGGTGGGAATCACCCCTTGCAGG CAG C SLC22A5 Ensembl:ENSG00000197375 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:132385938..132386120 26863196 MeRIP-seq:(Medium) rs1240617131 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_234343,RMVar_hsa_circ_114990 105245 RMVar_ID_105245 Human_SNP_ID_251757821 m1A Human chr5 - 132410733 132410733 132410733 CGGGGTGGAGCTGGGCCAGCCGAGTGCCCGAGAGCTAGTCCGCCACGCACACCTGCCTCGGCGGG CGGGGTGGAGCTGGGCCAGCCGAGTGCCCGAGGGCTAGTCCGCCACGCACACCTGCCTCGGCGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:132410596..132410768 26863196 MeRIP-seq:(Medium) rs1430796618 Functional Loss SNV dbSNP153 33..33 33 - - - 105246 RMVar_ID_105246 Human_SNP_ID_251790917 m1A Human chr5 + 132557334 132557334 132557334 TGAGATTAGAAACGTTTGCAAACATGTCCCGGATCGAAAAGATGAGCATTCTGGGCGTGCGGAGT TGAGATTAGAAACGTTTGCAAACATGTCCCGGGTCGAAAAGATGAGCATTCTGGGCGTGCGGAGT A G AC116366.3,RAD50 Ensembl:ENSG00000283782,Ensembl:ENSG00000113522 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:132557007..132557347 26863196 MeRIP-seq:(Medium) rs1060501972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1644059,Human_RBP_ID_1986177,Human_RBP_ID_4807809,Human_RBP_ID_9335311,Human_RBP_ID_15292698,Human_RBP_ID_23038317,Human_RBP_ID_24081957 Clinvar_Rec_676 RMVar_hsa_circ_13349 105247 RMVar_ID_105247 Human_SNP_ID_251825635 m1A Human chr5 - 132696280 132696280 132696280 CTACTGTATATTTAGGTAACTAGAATTTCAAAATAGAAAAAAAAAAACTGTGTCCTGTTTTGCAC CTACTGTATATTTAGGTAACTAGAATTTCAAAGTAGAAAAAAAAAAACTGTGTCCTGTTTTGCAC T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12514976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630828,Human_RBP_ID_5213322,Human_RBP_ID_10180574,Human_RBP_ID_25853343,Human_RBP_ID_26530452 105248 RMVar_ID_105248 Human_SNP_ID_251830241 m1A Human chr5 + 132715714 132715714 132715714 TTTTGTTAGAACAGTTAGTGGTTCAACAATGTATTTTTAGCCAACATAAAGATTAATATTTTGAG TTTTGTTAGAACAGTTAGTGGTTCAACAATGTGTTTTTAGCCAACATAAAGATTAATATTTTGAG A G AC004039.1 Ensembl:ENSG00000230612 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:132715700..132715854 26863196 MeRIP-seq:(Medium) rs1461066551 Functional Loss SNV dbSNP153 33..33 33 - - - 105249 RMVar_ID_105249 Human_SNP_ID_251835029 m1A Human chr5 - 132734438 132734438 132734438 ATCAGAGAAGCCAGAAAGCTGCGATAATGTGAAGGTTGTTGTTAGGTGCCGGCCCCTCAATGAGA ATCAGAGAAGCCAGAAAGCTGCGATAATGTGATGGTTGTTGTTAGGTGCCGGCCCCTCAATGAGA T A KIF3A Ensembl:ENSG00000131437 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132734388..132734494 26863196 MeRIP-seq:(Medium) rs763064050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1986323,Human_RBP_ID_24082150 Human_Splice_Rec_691388,Human_Splice_Rec_691420,Human_Splice_Rec_691454,Human_Splice_Rec_691502 RMVar_hsa_circ_357505,RMVar_hsa_circ_278099,RMVar_hsa_circ_306906,RMVar_hsa_circ_234374,RMVar_hsa_circ_234375,RMVar_hsa_circ_329468,RMVar_hsa_circ_342152,RMVar_hsa_circ_234378,RMVar_hsa_circ_321861 105250 RMVar_ID_105250 Human_SNP_ID_251835805 m1A Human chr5 + 132737499 132737499 132737499 CCAGCGACACCGGGTGCGCAGAAAGGATGGCCAGAGACTACCGAAACACCTCGTTGACGCTCTCG CCAGCGACACCGGGTGCGCAGAAAGGATGGCCTGAGACTACCGAAACACCTCGTTGACGCTCTCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132737296..132737513 26863196 MeRIP-seq:(Medium) rs1327685472 Functional Loss SNV dbSNP153 33..33 33 - - - 105251 RMVar_ID_105251 Human_SNP_ID_251839412 m1A Human chr5 - 132751961 132751961 132751961 GCCAGCTCAGGACCACCAGGGCATGGAACTGGAGACCATGGTTTTTAATGTTAGAACAGAAAACG GCCAGCTCAGGACCACCAGGGCATGGAACTGGGGACCATGGTTTTTAATGTTAGAACAGAAAACG T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132751910..132752061 32194978 MeRIP-seq:(Medium) rs768926275 Functional Loss SNV dbSNP153 33..33 33 - - - 105252 RMVar_ID_105252 Human_SNP_ID_251841803 m1A Human chr5 + 132761531 132761531 132761531 CTCCTCCAACTTGCAGCGCCGGTAGAGCTCGTAGTGCCGGCTGTGGGTCTGCTCGCGGAGGTCTT CTCCTCCAACTTGCAGCGCCGGTAGAGCTCGTGGTGCCGGCTGTGGGTCTGCTCGCGGAGGTCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:132761434..132761650 26863196 MeRIP-seq:(Medium) rs771312371 Functional Loss SNV dbSNP153 33..33 33 - - - 105253 RMVar_ID_105253 Human_SNP_ID_251841827 m1A Human chr5 + 132761572 132761572 132761572 TGTGGGTCTGCTCGCGGAGGTCTTCCATGTTCACCCGGATCAACATCTCCCGCAGCTTCACGAAG TGTGGGTCTGCTCGCGGAGGTCTTCCATGTTCGCCCGGATCAACATCTCCCGCAGCTTCACGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132761526..132761625 26863196 MeRIP-seq:(Medium) rs768233643 Functional Loss SNV dbSNP153 33..33 33 - - - 105254 RMVar_ID_105254 Human_SNP_ID_251842436 m1A Human chr5 - 132763854 132763854 132763854 GCCCATAGTTGACTACATCGATGCGCAGTTTGAAAATTATCTGCAGGAGGAGCTGAAGATCCGCC GCCCATAGTTGACTACATCGATGCGCAGTTTGGAAATTATCTGCAGGAGGAGCTGAAGATCCGCC T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:132762601..132763979 32194978 MeRIP-seq:(Medium) rs1357415474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126169 Human_Splice_Rec_691630 RMVar_hsa_circ_11562,RMVar_hsa_circ_88096,RMVar_hsa_circ_110676,RMVar_hsa_circ_234380,RMVar_hsa_circ_234379,RMVar_hsa_circ_48517,RMVar_hsa_circ_77060,RMVar_hsa_circ_234385 105255 RMVar_ID_105255 Human_SNP_ID_251845788 m1A Human chr5 - 132777137 132777137 132777137 TCCCAGCCCACCCGCCCGGTGCGGAGCTCGCCATGGCGGCCACCGACCTGGAGCGCTTCTCGGTG TCCCAGCCCACCCGCCCGGTGCGGAGCTCGCCGTGGCGGCCACCGACCTGGAGCGCTTCTCGGTG T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding start codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:132777117..132777267 32194978 MeRIP-seq:(Medium) rs1027902114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845931,Human_RBP_ID_9335313,Human_RBP_ID_22706009 Human_Splice_Rec_691573,Human_Splice_Rec_691591,Human_Splice_Rec_691607,Human_Splice_Rec_691623,Human_Splice_Rec_691659,Human_Splice_Rec_691693,Human_Splice_Rec_691709,Human_Splice_Rec_691745,Human_Splice_Rec_691749 RMVar_hsa_circ_110676,RMVar_hsa_circ_234379,RMVar_hsa_circ_77060,RMVar_hsa_circ_234385 105256 RMVar_ID_105256 Human_SNP_ID_251845803 m1A Human chr5 - 132777165 132777165 132777165 CTGGTCCCTGTCGCTGCCCCTGCGCTCGTCCCAGCCCACCCGCCCGGTGCGGAGCTCGCCATGGC CTGGTCCCTGTCGCTGCCCCTGCGCTCGTCCCGGCCCACCCGCCCGGTGCGGAGCTCGCCATGGC T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:132777060..132777180 26863196 MeRIP-seq:(Medium) rs1229692249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845932,Human_RBP_ID_9335313,Human_RBP_ID_18831997 Human_Splice_Rec_691573,Human_Splice_Rec_691591,Human_Splice_Rec_691607,Human_Splice_Rec_691623,Human_Splice_Rec_691659,Human_Splice_Rec_691693,Human_Splice_Rec_691709,Human_Splice_Rec_691745,Human_Splice_Rec_691749 RMVar_hsa_circ_110676,RMVar_hsa_circ_234379,RMVar_hsa_circ_77060,RMVar_hsa_circ_234385 105257 RMVar_ID_105257 Human_SNP_ID_251845821 m1A Human chr5 - 132777203 132777203 132777203 AGCCGCAGCCGCCCGGGCGGAGCGCGTCCCGCAGCCGGCTGGTCCCTGTCGCTGCCCCTGCGCTC AGCCGCAGCCGCCCGGGCGGAGCGCGTCCCGCGGCCGGCTGGTCCCTGTCGCTGCCCCTGCGCTC T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:132777066..132777342 26863196 MeRIP-seq:(Medium) rs190772633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250319,Human_RBP_ID_4808195,Human_RBP_ID_9335313 Human_Splice_Rec_691573,Human_Splice_Rec_691591,Human_Splice_Rec_691607,Human_Splice_Rec_691623,Human_Splice_Rec_691659,Human_Splice_Rec_691693,Human_Splice_Rec_691709,Human_Splice_Rec_691745,Human_Splice_Rec_691749 RMVar_hsa_circ_110676,RMVar_hsa_circ_234379,RMVar_hsa_circ_77060,RMVar_hsa_circ_234385 105258 RMVar_ID_105258 Human_SNP_ID_251858671 m1A Human chr5 - 132827108 132827108 132827108 TCTAAGCTGAGTCCTACAGGAGAAGCAAGAATAGAAGCAGGGCAAAGATGGGGGTCGGCCCATCA TCTAAGCTGAGTCCTACAGGAGAAGCAAGAATCGAAGCAGGGCAAAGATGGGGGTCGGCCCATCA T G SHROOM1 Ensembl:ENSG00000164403 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:132827057..132827263 26863196 MeRIP-seq:(Medium) rs138831932 Functional Loss SNV dbSNP153 33..33 33 - - - 105259 RMVar_ID_105259 Human_SNP_ID_251868256 m1A Human chr5 + 132866853 132866853 132866853 GCGCTTCGCGAAAGCGAGCCAAGCGCCTGTCCACCCTCGGTCCTGCAGGGCCGCCGCCACAATGG GCGCTTCGCGAAAGCGAGCCAAGCGCCTGTCCGCCCTCGGTCCTGCAGGGCCGCCGCCACAATGG A G UQCRQ Ensembl:ENSG00000164405 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:132866851..132866875 32194978 MeRIP-seq:(Medium) rs767629378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946978,Human_RBP_ID_5395668,Human_RBP_ID_23258959,Human_RBP_ID_27511131 RMVar_hsa_circ_234386,RMVar_hsa_circ_126084 105260 RMVar_ID_105260 Human_SNP_ID_251868260 m1A Human chr5 - 132866857 132866857 132866857 CGGCCCATTGTGGCGGCGGCCCTGCAGGACCGAGGGTGGACAGGCGCTTGGCTCGCTTTCGCGAA CGGCCCATTGTGGCGGCGGCCCTGCAGGACCGGGGGTGGACAGGCGCTTGGCTCGCTTTCGCGAA T C GDF9 Ensembl:ENSG00000164404 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:132866851..132866900 26863196 MeRIP-seq:(Medium) rs1024821976 Functional Loss SNV dbSNP153 33..33 33 - - - 105261 RMVar_ID_105261 Human_SNP_ID_251868267 m1A Human chr5 + 132866879 132866879 132866879 CTGTCCACCCTCGGTCCTGCAGGGCCGCCGCCACAATGGGCCGCGAGTTTGGGAATCTGACGCGG CTGTCCACCCTCGGTCCTGCAGGGCCGCCGCCCCAATGGGCCGCGAGTTTGGGAATCTGACGCGG A C UQCRQ Ensembl:ENSG00000164405 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:132866876..132866925 26863196 MeRIP-seq:(Medium) rs1201661557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788288,Human_RBP_ID_839929,Human_RBP_ID_1660675,Human_RBP_ID_1986352,Human_RBP_ID_3757198,Human_RBP_ID_4808246,Human_RBP_ID_5326539,Human_RBP_ID_5396724,Human_RBP_ID_8601989,Human_RBP_ID_9335316,Human_RBP_ID_17662698,Human_RBP_ID_18425266,Human_RBP_ID_18832007,Human_RBP_ID_22459240,Human_RBP_ID_23258959,Human_RBP_ID_24082243,Human_RBP_ID_26826495 Human_Splice_Rec_691852,Human_Splice_Rec_691856,Human_Splice_Rec_691860,Human_Splice_Rec_691866 RMVar_hsa_circ_234386,RMVar_hsa_circ_126084,RMVar_hsa_circ_234387,RMVar_hsa_circ_328451 105262 RMVar_ID_105262 Human_SNP_ID_251868268 m1A Human chr5 + 132866879 132866879 132866879 CTGTCCACCCTCGGTCCTGCAGGGCCGCCGCCACAATGGGCCGCGAGTTTGGGAATCTGACGCGG CTGTCCACCCTCGGTCCTGCAGGGCCGCCGCCGCAATGGGCCGCGAGTTTGGGAATCTGACGCGG A G UQCRQ Ensembl:ENSG00000164405 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:132866876..132866925 26863196 MeRIP-seq:(Medium) rs1201661557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788288,Human_RBP_ID_839929,Human_RBP_ID_1660675,Human_RBP_ID_1986352,Human_RBP_ID_3757198,Human_RBP_ID_4808246,Human_RBP_ID_5326539,Human_RBP_ID_5396724,Human_RBP_ID_8601989,Human_RBP_ID_9335316,Human_RBP_ID_17662698,Human_RBP_ID_18425266,Human_RBP_ID_18832007,Human_RBP_ID_22459240,Human_RBP_ID_23258959,Human_RBP_ID_24082243,Human_RBP_ID_26826495 Human_Splice_Rec_691852,Human_Splice_Rec_691856,Human_Splice_Rec_691860,Human_Splice_Rec_691866 RMVar_hsa_circ_234386,RMVar_hsa_circ_126084,RMVar_hsa_circ_234387,RMVar_hsa_circ_328451 105263 RMVar_ID_105263 Human_SNP_ID_251868308 m1A Human chr5 + 132866967 132866967 132866967 CTTGTCACCGTTCGAGCAGCGCGCCTATCCGCACGTCTTCACTAAAGGAATCCCCAATGTTCTGC CTTGTCACCGTTCGAGCAGCGCGCCTATCCGCGCGTCTTCACTAAAGGAATCCCCAATGTTCTGC A G UQCRQ Ensembl:ENSG00000164405 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:132866826..132867025 26863410 MeRIP-seq:(Medium) rs913604247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630983,Human_RBP_ID_4808246,Human_RBP_ID_5326833,Human_RBP_ID_8601992,Human_RBP_ID_17662898,Human_RBP_ID_18210398,Human_RBP_ID_22459678,Human_RBP_ID_22511366,Human_RBP_ID_26826501,Human_RBP_ID_27073607,Human_RBP_ID_27511132 Human_Splice_Rec_691852,Human_Splice_Rec_691853,Human_Splice_Rec_691856,Human_Splice_Rec_691860,Human_Splice_Rec_691861,Human_Splice_Rec_691863,Human_Splice_Rec_691866 RMVar_hsa_circ_234386,RMVar_hsa_circ_126084,RMVar_hsa_circ_234387,RMVar_hsa_circ_328451 105264 RMVar_ID_105264 Human_SNP_ID_251868327 m1A Human chr5 - 132866997 132866997 132866997 CCACGCGAAAGAAAGACTCCCGAATGCGGCGCAGAACATTGGGGATTCCTTTAGTGAAGACGTGC CCACGCGAAAGAAAGACTCCCGAATGCGGCGCCGAACATTGGGGATTCCTTTAGTGAAGACGTGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:132866976..132867000 26863196 MeRIP-seq:(Medium) rs562265918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15294483 105265 RMVar_ID_105265 Human_SNP_ID_251868530 m1A Human chr5 + 132867582 132867582 132867582 AAGAATCCAGCTGCCTATGAAAATGACAAATGAGCAACGCATCCGGATGACGGTTCCCTGTCTCT AAGAATCCAGCTGCCTATGAAAATGACAAATGGGCAACGCATCCGGATGACGGTTCCCTGTCTCT A G UQCRQ Ensembl:ENSG00000164405 Protein coding stop codon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1561469628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78532,Human_RBP_ID_250882,Human_RBP_ID_630989,Human_RBP_ID_1389970,Human_RBP_ID_1644207,Human_RBP_ID_1986356,Human_RBP_ID_3757204,Human_RBP_ID_4808255,Human_RBP_ID_5121372,Human_RBP_ID_7381835,Human_RBP_ID_8267308,Human_RBP_ID_8601997,Human_RBP_ID_9169301,Human_RBP_ID_9398133,Human_RBP_ID_15294498,Human_RBP_ID_17526984,Human_RBP_ID_17662703,Human_RBP_ID_18057271,Human_RBP_ID_18832013,Human_RBP_ID_24082251,Human_RBP_ID_26350523,Human_RBP_ID_26520887,Human_RBP_ID_26826507,Human_RBP_ID_27330968 Human_Splice_Rec_691854,Human_Splice_Rec_691858,Human_Splice_Rec_691862,Human_Splice_Rec_691864 105266 RMVar_ID_105266 Human_SNP_ID_251885415 m1A Human chr5 + 132934939 132934939 132934939 TGAATACGACTTGATAACTTATCTTCTTTGCTAGTCTACAAAAAAATAAAATAAAATAAAATTAT TGAATACGACTTGATAACTTATCTTCTTTGCTTGTCTACAAAAAAATAAAATAAAATAAAATTAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:132934784..132934977 26863196 MeRIP-seq:(Medium) rs1418324753 Functional Loss SNV dbSNP153 33..33 33 - - - 105267 RMVar_ID_105267 Human_SNP_ID_251886063 m1A Human chr5 - 132937151 132937151 132937151 CGTGAAGACCGGAATGTGCTGCGTATGAAAGAACGGGAAAGGCGGAATCAGGAAATTCAGCAGGG CGTGAAGACCGGAATGTGCTGCGTATGAAAGAGCGGGAAAGGCGGAATCAGGAAATTCAGCAGGG T C AFF4 Ensembl:ENSG00000072364 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:132934830..132963601;chr5:132934815..132963604;chr5:132937013..132937254 26863196 MeRIP-seq:(Medium) rs1207857395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838639,Human_RBP_ID_944506,Human_RBP_ID_5610298,Human_RBP_ID_9399349,Human_RBP_ID_15295828,Human_RBP_ID_22681645,Human_RBP_ID_24082473,Human_RBP_ID_24547989,Human_RBP_ID_24561983,Human_RBP_ID_25933320 Human_Splice_Rec_691878,Human_Splice_Rec_691879,Human_Splice_Rec_691918,Human_Splice_Rec_691919,Human_Splice_Rec_691988,Human_Splice_Rec_691989,Human_Splice_Rec_692000,Human_Splice_Rec_692001,Human_Splice_Rec_692008,Human_Splice_Rec_692009 RMVar_hsa_circ_79415,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_70765,RMVar_hsa_circ_274107,RMVar_hsa_circ_234407,RMVar_hsa_circ_234408,RMVar_hsa_circ_365681,RMVar_hsa_circ_234411 105268 RMVar_ID_105268 Human_SNP_ID_251893466 m1A Human chr5 - 132963253 132963253 132963253 TCGGGCCTAGCGGAGCCGGGACTGGAGGTAAGAAGGGCCGACAGACTGACCCAGGGCCGGGCCGG TCGGGCCTAGCGGAGCCGGGACTGGAGGTAAGCAGGGCCGACAGACTGACCCAGGGCCGGGCCGG T G AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:132963251..132963300 26863196 MeRIP-seq:(Medium) rs1335304327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124659,Human_RBP_ID_26792112 105269 RMVar_ID_105269 Human_SNP_ID_251902508 m1A Human chr5 - 132997818 132997818 132997818 AAAGAAAGCAGCCATGTAAGAGGCTAACTTAAATAGAAGTGCTAGAAATATCTTTGTGTATTAAC AAAGAAAGCAGCCATGTAAGAGGCTAACTTAAGTAGAAGTGCTAGAAATATCTTTGTGTATTAAC T C ZCCHC10 Ensembl:ENSG00000155329 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3210524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2363741 RMVar_hsa_circ_78262,RMVar_hsa_circ_234412 105270 RMVar_ID_105270 Human_SNP_ID_251910122 m1A Human chr5 + 133026429 133026429 133026429 ACATTCTCCGCCGGTCCCAATAGGGGTCCGACACCAGCCCGTTGACGCGCGTTTCCCCGCTCCCA ACATTCTCCGCCGGTCCCAATAGGGGTCCGACCCCAGCCCGTTGACGCGCGTTTCCCCGCTCCCA A C AC113410.6 Ensembl:ENSG00000287054 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:133026424..133026515 26863196 MeRIP-seq:(Medium) rs960014342 Functional Loss SNV dbSNP153 33..33 33 - - - 105271 RMVar_ID_105271 Human_SNP_ID_251917259 m1A Human chr5 + 133052093 133052093 133052093 CCGGAGCCGGCCTGAGCAGCGCTCTCGGTTGCAGTACCCACTGGAAGGACTTAGGCGCTCGCGTG CCGGAGCCGGCCTGAGCAGCGCTCTCGGTTGCCGTACCCACTGGAAGGACTTAGGCGCTCGCGTG A C HSPA4 Ensembl:ENSG00000170606 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:133052043..133052164 26863196 MeRIP-seq:(Medium) rs147244562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_631145,Human_RBP_ID_1319146,Human_RBP_ID_1644299,Human_RBP_ID_4808556,Human_RBP_ID_5215985,Human_RBP_ID_5426840,Human_RBP_ID_5449287,Human_RBP_ID_5476194,Human_RBP_ID_5508811,Human_RBP_ID_8602138,Human_RBP_ID_8883963,Human_RBP_ID_9306588,Human_RBP_ID_9335318,Human_RBP_ID_15296404,Human_RBP_ID_26826511 RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417 105272 RMVar_ID_105272 Human_SNP_ID_251919024 m1A Human chr5 + 133057956 133057956 133057956 TGAGTCCAATTATGGACAAGGCTGTGTGATACAGACCTAAAATACCATGTTCAAAGGAGATGTAA TGAGTCCAATTATGGACAAGGCTGTGTGATACGGACCTAAAATACCATGTTCAAAGGAGATGTAA A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:133057952..133058056 26863196 MeRIP-seq:(Medium) rs1458445787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417 105273 RMVar_ID_105273 Human_SNP_ID_251920237 m1A Human chr5 + 133062218 133062218 133062218 TTGGTTTTGTTTGGAAGGTAATTAGAAGCAAGACAGTTTCAGAGTTACTGACATAGAATAGGAAA TTGGTTTTGTTTGGAAGGTAATTAGAAGCAAGGCAGTTTCAGAGTTACTGACATAGAATAGGAAA A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:133062215..133062391 26863196 MeRIP-seq:(Medium) rs935210936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15296645 RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417 105274 RMVar_ID_105274 Human_SNP_ID_251928568 m1A Human chr5 - 133092732 133092732 133092732 TTTTCTGCTGGTGTCTGCTGCTGTTGCTCTTCAACATGTGGTTCCTCCTGGTCCACTTGCATCTT TTTTCTGCTGGTGTCTGCTGCTGTTGCTCTTCCACATGTGGTTCCTCCTGGTCCACTTGCATCTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:133092701..133092800 32194978 MeRIP-seq:(Medium) rs1203602044 Functional Loss SNV dbSNP153 33..33 33 - - - 105275 RMVar_ID_105275 Human_SNP_ID_252136339 m1A Human chr5 + 133972224 133972224 133972224 AGGAATAAGTCCTGAATTATTGGCTTCATCACATCCACCTTCTCCACCCCAAAATGGCACAAAAG AGGAATAAGTCCTGAATTATTGGCTTCATCACCTCCACCTTCTCCACCCCAAAATGGCACAAAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:133972173..133972281 26863196 MeRIP-seq:(Medium) rs528540612 Functional Loss SNV dbSNP153 33..33 33 - - - 105276 RMVar_ID_105276 Human_SNP_ID_252138282 m1A Human chr5 + 133980872 133980872 133980872 TCGTAACCTAGCACCAGAGCACCCCGGATGGAAGGCCCAGCAATGTCGAAATCCATGTCGCAGCC TCGTAACCTAGCACCAGAGCACCCCGGATGGACGGCCCAGCAATGTCGAAATCCATGTCGCAGCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:133980826..133981003 32194978 MeRIP-seq:(Medium) rs777712191 Functional Loss SNV dbSNP153 33..33 33 - - - 105277 RMVar_ID_105277 Human_SNP_ID_252171222 m1A Human chr5 - 134114850 134114832 134114850 GGGGCGCTGGGCGCCGGGAGTGCGGGGCGCGGAGCCGGCCCGGGGGGCGGCGAGCCCGGAGTCCG GGGGCGCTGGGCGCCGGGAGTGCGGGGCGCGG__________________CGAGCCCGGAGTCCG GCCGCCCCCCGGGCCGGCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134114807..134114918 26863196 MeRIP-seq:(Medium) rs1346990161 Functional Loss DEL dbSNP153 33..50 33 - - - 105278 RMVar_ID_105278 Human_SNP_ID_252177856 m1A Human chr5 + 134140846 134140846 134140846 CCCCCTGTCCCCTTCCTGCGGATATAGACAGCACTTCCCTGCCCCCACTGCAGCCCCTGGCGCCC CCCCCTGTCCCCTTCCTGCGGATATAGACAGCGCTTCCCTGCCCCCACTGCAGCCCCTGGCGCCC A G TCF7 Ensembl:ENSG00000081059 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134140795..134140955 26863196 MeRIP-seq:(Medium) rs1412167768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_692452,Human_Splice_Rec_692453,Human_Splice_Rec_692466,Human_Splice_Rec_692467,Human_Splice_Rec_692486,Human_Splice_Rec_692487,Human_Splice_Rec_692568,Human_Splice_Rec_692569,Human_Splice_Rec_692580,Human_Splice_Rec_692581,Human_Splice_Rec_692598,Human_Splice_Rec_692599,Human_Splice_Rec_692607 105279 RMVar_ID_105279 Human_SNP_ID_252179143 m1A Human chr5 - 134144766 134144766 134144766 GTCTGCTCACAGCCATGCCAGAGGGGTAGAGCAGGGCAGAGGGCGAGCAGGCAGCGGGGCAGAGC GTCTGCTCACAGCCATGCCAGAGGGGTAGAGCCGGGCAGAGGGCGAGCAGGCAGCGGGGCAGAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134144763..134144853 26863196 MeRIP-seq:(Medium) rs756603729 Functional Loss SNV dbSNP153 33..33 33 - - - 105280 RMVar_ID_105280 Human_SNP_ID_252179676 m1A Human chr5 - 134146301 134146301 134146301 AGTCCTGGGGAGCTGGGGACCCGGGGCAGCCTAGAGCACTGTCATCGGAAGGAACGGGGCTGGGG AGTCCTGGGGAGCTGGGGACCCGGGGCAGCCTGGAGCACTGTCATCGGAAGGAACGGGGCTGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134146261..134146397 26863196 MeRIP-seq:(Medium) rs1336155679 Functional Loss SNV dbSNP153 33..33 33 - - - 105281 RMVar_ID_105281 Human_SNP_ID_252184406 m1A Human chr5 + 134163814 134163814 134163814 CCTATCTCAAACAAACAAACCAAACAAACAAAAAAACCCCAAAAACCAAGCACTTCTCATTCTCA CCTATCTCAAACAAACAAACCAAACAAACAAACAAACCCCAAAAACCAAGCACTTCTCATTCTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134163811..134163947 26863196 MeRIP-seq:(Medium) rs1333151336 Functional Loss SNV dbSNP153 33..33 33 - - - 105282 RMVar_ID_105282 Human_SNP_ID_252185347 m1A Human chr5 - 134167245 134167245 134167245 TTAGGAAATAGAAACTTTCTTCTGGTTTTCTTAGATTTGGGAATGGATGATGAAGGAGATGATGA TTAGGAAATAGAAACTTTCTTCTGGTTTTCTTGGATTTGGGAATGGATGATGAAGGAGATGATGA T C SKP1,AC104109.3 Ensembl:ENSG00000113558,Ensembl:ENSG00000272772 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134167220..134167297 26863196 MeRIP-seq:(Medium) rs901063367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2894936,Human_RBP_ID_4809006,Human_RBP_ID_10181311,Human_RBP_ID_17527112,Human_RBP_ID_18056864,Human_RBP_ID_22680687 Human_Splice_Rec_692655,Human_Splice_Rec_692665,Human_Splice_Rec_692673,Human_Splice_Rec_692687,Human_Splice_Rec_692699,Human_Splice_Rec_692711,Human_Splice_Rec_692721,Human_Splice_Rec_692735,Human_Splice_Rec_692743,Human_Splice_Rec_692751 RMVar_hsa_circ_378921,RMVar_hsa_circ_1017,RMVar_hsa_circ_234465,RMVar_hsa_circ_234461,RMVar_hsa_circ_377328,RMVar_hsa_circ_300155,RMVar_hsa_circ_234466,RMVar_hsa_circ_25318,RMVar_hsa_circ_59352,RMVar_hsa_circ_322291,RMVar_hsa_circ_234467,RMVar_hsa_circ_351772,RMVar_hsa_circ_234468 105283 RMVar_ID_105283 Human_SNP_ID_252187179 m1A Human chr5 - 134174024 134174017 134174024 CTTAAATTTTATATTTAATGTCCTTTTTTTTTAGATGCCTTCAATTAAGTTGCAGAGTTCTGATG CTTAAATTTTATATTTAATGTCCTTTTTTTTT_______TTCAATTAAGTTGCAGAGTTCTGATG AGGCATCT A SKP1,AC104109.3 Ensembl:ENSG00000113558,Ensembl:ENSG00000272772 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134174001..134174025 26863196 MeRIP-seq:(Medium) rs1487231678 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_74562 Human_Splice_Rec_692653,Human_Splice_Rec_692663,Human_Splice_Rec_692671,Human_Splice_Rec_692685,Human_Splice_Rec_692695,Human_Splice_Rec_692709,Human_Splice_Rec_692719,Human_Splice_Rec_692731,Human_Splice_Rec_692741,Human_Splice_Rec_692749,Human_Splice_Rec_692761 RMVar_hsa_circ_1017,RMVar_hsa_circ_25318,RMVar_hsa_circ_59352,RMVar_hsa_circ_122467,RMVar_hsa_circ_234470 105284 RMVar_ID_105284 Human_SNP_ID_252200032 m1A Human chr5 + 134223681 134223681 134223681 ATTAGATGCATCAGCTTCACCCACCCCACTCTAGCATCCAGTATTATCTTATCTTCTACAACAGT ATTAGATGCATCAGCTTCACCCACCCCACTCTGGCATCCAGTATTATCTTATCTTCTACAACAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134223679..134223758 26863196 MeRIP-seq:(Medium) rs879623048 Functional Loss SNV dbSNP153 33..33 33 - - - 105285 RMVar_ID_105285 Human_SNP_ID_252200704 m1A Human chr5 - 134225800 134225800 134225800 GGACCAGTGGATCGAGCAGCTGAACGAGTGCAAGCAGCTGTCCGAGTCCCAGGTCAAGAGCCTCT GGACCAGTGGATCGAGCAGCTGAACGAGTGCAGGCAGCTGTCCGAGTCCCAGGTCAAGAGCCTCT T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding CDS,intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:134167151..134225925 32194978 MeRIP-seq:(Medium) rs142542860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77377,Human_RBP_ID_1038774,Human_RBP_ID_1141466,Human_RBP_ID_1644593,Human_RBP_ID_4849329,Human_RBP_ID_5090212,Human_RBP_ID_5267703,Human_RBP_ID_5656148,Human_RBP_ID_7384484,Human_RBP_ID_8236953,Human_RBP_ID_8602658,Human_RBP_ID_8893650,Human_RBP_ID_9335326,Human_RBP_ID_9398164,Human_RBP_ID_18832417,Human_RBP_ID_21900705,Human_RBP_ID_22458917,Human_RBP_ID_23050419,Human_RBP_ID_26351269,Human_RBP_ID_26521228 Human_Splice_Rec_692759,Human_Splice_Rec_692763,Human_Splice_Rec_692789 105286 RMVar_ID_105286 Human_SNP_ID_252200741 m1A Human chr5 + 134225877 134225877 134225877 AACACCTTCTCGTCCATGATGCCACCCGCCCCAGCCGGCTGCCGCTCCGCGCTGCTCCCGCGCCG AACACCTTCTCGTCCATGATGCCACCCGCCCCGGCCGGCTGCCGCTCCGCGCTGCTCCCGCGCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:134225826..134226075 26863196 MeRIP-seq:(Medium) rs1289086008 Functional Loss SNV dbSNP153 33..33 33 - - - 105287 RMVar_ID_105287 Human_SNP_ID_252200752 m1A Human chr5 - 134225897 134225897 134225897 GTAGGCCCGTGTGCGGGCGGCGGCGCGGGAGCAGCGCGGAGCGGCAGCCGGCTGGGGCGGGTGGC GTAGGCCCGTGTGCGGGCGGCGGCGCGGGAGCGGCGCGGAGCGGCAGCCGGCTGGGGCGGGTGGC T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding 5'UTR,intron,5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:134225804..134226071 26863196 MeRIP-seq:(Medium) rs377165125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77377,Human_RBP_ID_250536,Human_RBP_ID_788659,Human_RBP_ID_1660502,Human_RBP_ID_3785036,Human_RBP_ID_4809135,Human_RBP_ID_5090188,Human_RBP_ID_5214430,Human_RBP_ID_5656148,Human_RBP_ID_8214982,Human_RBP_ID_9306596,Human_RBP_ID_9335326,Human_RBP_ID_9398164,Human_RBP_ID_22459247,Human_RBP_ID_23050419,Human_RBP_ID_26351269 105288 RMVar_ID_105288 Human_SNP_ID_252200781 m1A Human chr5 - 134225974 134225974 134225974 GCGGTGAGAGCCAGCGGGCCAGCGCCAGCCTCAACAGCCGCCAGAAGTACACGAGGAACCGGCGG GCGGTGAGAGCCAGCGGGCCAGCGCCAGCCTCTACAGCCGCCAGAAGTACACGAGGAACCGGCGG T A PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding 5'UTR,intron,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:134225751..134226092 26863410 MeRIP-seq:(Medium) rs1294668999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77377,Human_RBP_ID_250537,Human_RBP_ID_945108,Human_RBP_ID_1644599,Human_RBP_ID_1986750,Human_RBP_ID_4809136,Human_RBP_ID_8602662,Human_RBP_ID_18832423 105289 RMVar_ID_105289 Human_SNP_ID_252234991 m1A Human chr5 + 134371630 134371630 134371630 GTCGACCCCGGCCCGGAGGAGGCTCATGCGGGATTTCAAGCGGTAAGGGCCTTCACCTTCGCCTA GTCGACCCCGGCCCGGAGGAGGCTCATGCGGGGTTTCAAGCGGTAAGGGCCTTCACCTTCGCCTA A G UBE2B Ensembl:ENSG00000119048 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:134371204..134371684;chr5:134371224..134380800;chr5:134371226..134374475 26863196 MeRIP-seq:(Medium) rs1305512957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_631534,Human_RBP_ID_944512,Human_RBP_ID_1038777,Human_RBP_ID_4845956,Human_RBP_ID_5151127 Human_Splice_Rec_692963,Human_Splice_Rec_692969,Human_Splice_Rec_692973,Human_Splice_Rec_692983,Human_Splice_Rec_692995,Human_Splice_Rec_693005 105290 RMVar_ID_105290 Human_SNP_ID_252237463 m1A Human chr5 + 134380753 134380753 134380753 ACTTTTAAACTAGTAATAGAATTTTCTGAAGAATATCCAAATAAACCACCAACTGTTAGGTTTTT ACTTTTAAACTAGTAATAGAATTTTCTGAAGACTATCCAAATAAACCACCAACTGTTAGGTTTTT A C UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134380751..134380775 26863196 MeRIP-seq:(Medium) rs749410915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78080,Human_RBP_ID_631536,Human_RBP_ID_1038778,Human_RBP_ID_1986768,Human_RBP_ID_7384677,Human_RBP_ID_8132508,Human_RBP_ID_8267322,Human_RBP_ID_15301413,Human_RBP_ID_17297823,Human_RBP_ID_17411439,Human_RBP_ID_17527151,Human_RBP_ID_17706963,Human_RBP_ID_18038657,Human_RBP_ID_18537716,Human_RBP_ID_18832452,Human_RBP_ID_27511298,Human_RBP_ID_27567187,Human_RBP_ID_27734552 Human_Splice_Rec_692978,Human_Splice_Rec_692979,Human_Splice_Rec_692988,Human_Splice_Rec_692989,Human_Splice_Rec_693000,Human_Splice_Rec_693001 RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 105291 RMVar_ID_105291 Human_SNP_ID_252242508 m1A Human chr5 - 134402378 134402378 134402378 CCTTTTTGGGCTGGGCACAGTGGCTTATGCCCATAATAATCCCAGCACTTTGGGAGGCCGAGGTG CCTTTTTGGGCTGGGCACAGTGGCTTATGCCCGTAATAATCCCAGCACTTTGGGAGGCCGAGGTG T C CDKN2AIPNL Ensembl:ENSG00000237190 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:134402330..134402428 32194978 MeRIP-seq:(Medium) rs1182209570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_631580,Human_RBP_ID_1210582,Human_RBP_ID_10181740,Human_RBP_ID_18038707,Human_RBP_ID_23038670,Human_RBP_ID_23214274,Human_RBP_ID_24503315,Human_RBP_ID_26529248 105292 RMVar_ID_105292 Human_SNP_ID_252244759 m1A Human chr5 - 134411820 134411820 134411820 GGTCGGTGGCGAGGCGGCTGCCGCAGTGGAGGAGCTGGTTTCGGGGGTGCGGCAGGCGGCCGACT GGTCGGTGGCGAGGCGGCTGCCGCAGTGGAGGCGCTGGTTTCGGGGGTGCGGCAGGCGGCCGACT T G CDKN2AIPNL Ensembl:ENSG00000237190 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:134411512..134411900;chr5:134411651..134411900 26863196 MeRIP-seq:(Medium) rs1477431606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845355,Human_RBP_ID_7384911,Human_RBP_ID_18038719,Human_RBP_ID_22099593,Human_RBP_ID_24083320 105293 RMVar_ID_105293 Human_SNP_ID_252272377 m1A Human chr5 + 134525277 134525275 134525277 GTGAAAGAGTGGAGGGGCGGGGTATGTGTGTGAGTGTGTGAAGTGTGAGCAGACCTGATGGGACT GTGAAAGAGTGGAGGGGCGGGGTATGTGTGT__GTGTGTGAAGTGTGAGCAGACCTGATGGGACT TGA T JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134525227..134525428 26863196 MeRIP-seq:(Medium) rs977599205 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18465212 105294 RMVar_ID_105294 Human_SNP_ID_252272378 m1A Human chr5 + 134525277 134525277 134525277 GTGAAAGAGTGGAGGGGCGGGGTATGTGTGTGAGTGTGTGAAGTGTGAGCAGACCTGATGGGACT GTGAAAGAGTGGAGGGGCGGGGTATGTGTGTGTGTGTGTGAAGTGTGAGCAGACCTGATGGGACT A T JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134525227..134525428 26863196 MeRIP-seq:(Medium) rs926153585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18465212 105295 RMVar_ID_105295 Human_SNP_ID_252272558 m1A Human chr5 - 134525735 134525735 134525735 AAGTAACTCCATGGACGCTACTCACCCCCCCCAAAAAATAGCCTCCAACTGCGATGGCCGCGGTC AAGTAACTCCATGGACGCTACTCACCCCCCCCCAAAAATAGCCTCCAACTGCGATGGCCGCGGTC T G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134525689..134525872 26863196 MeRIP-seq:(Medium) rs1173625771 Functional Loss SNV dbSNP153 33..33 33 - - - 105296 RMVar_ID_105296 Human_SNP_ID_252272574 m1A Human chr5 - 134525744 134525743 134525744 GTGGGCGCAAAGTAACTCCATGGACGCTACTCACCCCCCCCAAAAAATAGCCTCCAACTGCGATG GTGGGCGCAAAGTAACTCCATGGACGCTACTC_CCCCCCCCAAAAAATAGCCTCCAACTGCGATG GT G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134525700..134525860 26863196 MeRIP-seq:(Medium) rs1561716509 Functional Loss DEL dbSNP153 33..33 33 - - - 105297 RMVar_ID_105297 Human_SNP_ID_252272596 m1A Human chr5 + 134525810 134525810 134525810 CCTAGCGGCACCGGCTTAGGTCCTGCGGGCCGACCGTCCCCGGCGGGGGGCGTGGGGCCTGGGAC CCTAGCGGCACCGGCTTAGGTCCTGCGGGCCGGCCGTCCCCGGCGGGGGGCGTGGGGCCTGGGAC A G JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:134525760..134525895 26863196 MeRIP-seq:(Medium) rs1259794657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18501773 RMVar_hsa_circ_89877,RMVar_hsa_circ_234507 105298 RMVar_ID_105298 Human_SNP_ID_252272761 m1A Human chr5 + 134526210 134526210 134526210 GGGATGCACAGCACAGGGGAGAGAGATTGCGCATGTTGGTCAGTCGTGTTTTAAAGAGTACAGTG GGGATGCACAGCACAGGGGAGAGAGATTGCGCTTGTTGGTCAGTCGTGTTTTAAAGAGTACAGTG A T JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134526204..134526269 26863196 MeRIP-seq:(Medium) rs1477245146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_693105 RMVar_hsa_circ_89877,RMVar_hsa_circ_234507 105299 RMVar_ID_105299 Human_SNP_ID_252272876 m1A Human chr5 - 134526561 134526561 134526561 GGACCGGCTGCACGTGAGCCCAGCGCGAGGTCATGTGCACCGGCTCAGCCCGGTTCGGCGCCCGG GGACCGGCTGCACGTGAGCCCAGCGCGAGGTCTTGTGCACCGGCTCAGCCCGGTTCGGCGCCCGG T A RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134526558..134527109 26863196 MeRIP-seq:(Medium) rs569069701 Functional Loss SNV dbSNP153 33..33 33 - - - 105300 RMVar_ID_105300 Human_SNP_ID_252272877 m1A Human chr5 - 134526561 134526561 134526561 GGACCGGCTGCACGTGAGCCCAGCGCGAGGTCATGTGCACCGGCTCAGCCCGGTTCGGCGCCCGG GGACCGGCTGCACGTGAGCCCAGCGCGAGGTCCTGTGCACCGGCTCAGCCCGGTTCGGCGCCCGG T G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134526558..134527109 26863196 MeRIP-seq:(Medium) rs569069701 Functional Loss SNV dbSNP153 33..33 33 - - - 105301 RMVar_ID_105301 Human_SNP_ID_252272881 m1A Human chr5 - 134526577 134526577 134526577 GAAGGTGTCTGGGACCGGACCGGCTGCACGTGAGCCCAGCGCGAGGTCATGTGCACCGGCTCAGC GAAGGTGTCTGGGACCGGACCGGCTGCACGTGCGCCCAGCGCGAGGTCATGTGCACCGGCTCAGC T G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134526549..134526812 26863196 MeRIP-seq:(Medium) rs1341479122 Functional Loss SNV dbSNP153 33..33 33 - - - 105302 RMVar_ID_105302 Human_SNP_ID_252275097 m1A Human chr5 + 134535096 134535096 134535096 TGTAAATGGAGCTCACAGCTCACCTGGTTAGGAACAGGAGATGATGTGGATAAAGGAAGACTCCG TGTAAATGGAGCTCACAGCTCACCTGGTTAGGGACAGGAGATGATGTGGATAAAGGAAGACTCCG A G JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134535089..134535239 26863196 MeRIP-seq:(Medium) rs1259798704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89877,RMVar_hsa_circ_234507 105303 RMVar_ID_105303 Human_SNP_ID_252275102 m1A Human chr5 + 134535116 134535116 134535116 CACCTGGTTAGGAACAGGAGATGATGTGGATAAAGGAAGACTCCGCGTGAGCTCAGTATGAGGCC CACCTGGTTAGGAACAGGAGATGATGTGGATATAGGAAGACTCCGCGTGAGCTCAGTATGAGGCC A T JADE2 Ensembl:ENSG00000043143 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134535113..134535226 26863196 MeRIP-seq:(Medium) rs1479477410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89877,RMVar_hsa_circ_234507 105304 RMVar_ID_105304 Human_SNP_ID_252281786 m1A Human chr5 + 134560842 134560842 134560842 CCAGAATATGGCCAGGGCCATTGAGACGCAGGAGGGGCTGGGCATCGAGTACGACGAGGATGTTG CCAGAATATGGCCAGGGCCATTGAGACGCAGGGGGGGCTGGGCATCGAGTACGACGAGGATGTTG A G JADE2 Ensembl:ENSG00000043143 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134560705..134560982 26863196 MeRIP-seq:(Medium) rs750625307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_693050,Human_Splice_Rec_693076,Human_Splice_Rec_693094,Human_Splice_Rec_693114,Human_Splice_Rec_693134,Human_Splice_Rec_693142 RMVar_hsa_circ_29743,RMVar_hsa_circ_64432,RMVar_hsa_circ_89877,RMVar_hsa_circ_234507,RMVar_hsa_circ_313837,RMVar_hsa_circ_125756,RMVar_hsa_circ_1269,RMVar_hsa_circ_50840,RMVar_hsa_circ_7573,RMVar_hsa_circ_114599,RMVar_hsa_circ_83541,RMVar_hsa_circ_234510,RMVar_hsa_circ_374840,RMVar_hsa_circ_234511,RMVar_hsa_circ_124683,RMVar_hsa_circ_234514,RMVar_hsa_circ_80956,RMVar_hsa_circ_29663,RMVar_hsa_circ_234515,RMVar_hsa_circ_234512,RMVar_hsa_circ_234513,RMVar_hsa_circ_81818,RMVar_hsa_circ_234516 105305 RMVar_ID_105305 Human_SNP_ID_252283407 m1A Human chr5 - 134567109 134567107 134567109 TGCCTCTGTTCTGTTTGCCCAGCACCCCACGGAGCCGCGTTTACCCATCTACCCTGCCCTGGCCC TGCCTCTGTTCTGTTTGCCCAGCACCCCACGG__CCGCGTTTACCCATCTACCCTGCCCTGGCCC GCT G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134567102..134567272 26863196 MeRIP-seq:(Medium) rs994071076 Functional Loss DEL dbSNP153 33..34 33 - - - 105306 RMVar_ID_105306 Human_SNP_ID_252285128 m1A Human chr5 + 134573761 134573761 134573761 CAGATGAAACTTATTGAACAGGATCTGTGTCGAGGTAGGCGCCTTCCCCACCTGCCGCCGCCACC CAGATGAAACTTATTGAACAGGATCTGTGTCGTGGTAGGCGCCTTCCCCACCTGCCGCCGCCACC A T JADE2 Ensembl:ENSG00000043143 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134573736..134573820 26863196 MeRIP-seq:(Medium) rs1323670312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124675 Human_Splice_Rec_693059,Human_Splice_Rec_693085,Human_Splice_Rec_693123,Human_Splice_Rec_693147 RMVar_hsa_circ_89877,RMVar_hsa_circ_234507,RMVar_hsa_circ_125756,RMVar_hsa_circ_50840,RMVar_hsa_circ_114599,RMVar_hsa_circ_83541,RMVar_hsa_circ_234510,RMVar_hsa_circ_234511,RMVar_hsa_circ_124683,RMVar_hsa_circ_234514,RMVar_hsa_circ_234515,RMVar_hsa_circ_81818,RMVar_hsa_circ_104954,RMVar_hsa_circ_125215,RMVar_hsa_circ_234516,RMVar_hsa_circ_234517,RMVar_hsa_circ_95501,RMVar_hsa_circ_234518,RMVar_hsa_circ_234519 105307 RMVar_ID_105307 Human_SNP_ID_252286438 m1A Human chr5 + 134578768 134578768 134578768 ACCCGCCTGCCTGCCAAGAAGAAACCACCACCACCACCACCGCAGGACGGGCCTGGTTCACGGAC ACCCGCCTGCCTGCCAAGAAGAAACCACCACCGCCACCACCGCAGGACGGGCCTGGTTCACGGAC A G JADE2 Ensembl:ENSG00000043143 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134578719..134578814 26863196 MeRIP-seq:(Medium) rs755306072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27511321 RMVar_hsa_circ_89877,RMVar_hsa_circ_234507,RMVar_hsa_circ_125756,RMVar_hsa_circ_83541,RMVar_hsa_circ_234510,RMVar_hsa_circ_234511,RMVar_hsa_circ_124683,RMVar_hsa_circ_234515,RMVar_hsa_circ_81818,RMVar_hsa_circ_86130,RMVar_hsa_circ_104954,RMVar_hsa_circ_125215,RMVar_hsa_circ_234516,RMVar_hsa_circ_234517,RMVar_hsa_circ_95501,RMVar_hsa_circ_234518,RMVar_hsa_circ_234519,RMVar_hsa_circ_234520 105308 RMVar_ID_105308 Human_SNP_ID_252286445 m1A Human chr5 + 134578782 134578782 134578782 CAAGAAGAAACCACCACCACCACCACCGCAGGACGGGCCTGGTTCACGGACGACTCCAGACAAAG CAAGAAGAAACCACCACCACCACCACCGCAGGTCGGGCCTGGTTCACGGACGACTCCAGACAAAG A T JADE2 Ensembl:ENSG00000043143 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134578731..134578930 26863196 MeRIP-seq:(Medium) rs1256251867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27511321 RMVar_hsa_circ_89877,RMVar_hsa_circ_234507,RMVar_hsa_circ_125756,RMVar_hsa_circ_234510,RMVar_hsa_circ_124683,RMVar_hsa_circ_234515,RMVar_hsa_circ_81818,RMVar_hsa_circ_86130,RMVar_hsa_circ_104954,RMVar_hsa_circ_125215,RMVar_hsa_circ_234516,RMVar_hsa_circ_234517,RMVar_hsa_circ_95501,RMVar_hsa_circ_234518,RMVar_hsa_circ_234519,RMVar_hsa_circ_234520 105309 RMVar_ID_105309 Human_SNP_ID_252286539 m1A Human chr5 - 134578971 134578971 134578971 CTGAGGCTGCCTCGTCCGGGGTCTCAGGGGCCAGTGGCGGGGGGCTTTCAGGGGTGGCTAGGATG CTGAGGCTGCCTCGTCCGGGGTCTCAGGGGCCTGTGGCGGGGGGCTTTCAGGGGTGGCTAGGATG T A RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134578951..134578975 26863196 MeRIP-seq:(Medium) rs955235691 Functional Loss SNV dbSNP153 33..33 33 - - - 105310 RMVar_ID_105310 Human_SNP_ID_252303447 m1A Human chr5 + 134648654 134648654 134648654 CCGGGCACGGTCGTCGGGGTCGGGGCACCAGGAGCTGTCAGGTGGCCTCGGGGCAGCCCGGCTGG CCGGGCACGGTCGTCGGGGTCGGGGCACCAGGGGCTGTCAGGTGGCCTCGGGGCAGCCCGGCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134648604..134648710 26863196 MeRIP-seq:(Medium) rs1238223863 Functional Loss SNV dbSNP153 33..33 33 - - - 105311 RMVar_ID_105311 Human_SNP_ID_252326112 m1A Human chr5 + 134738697 134738697 134738697 GGTCCCAGCGGGCTCAGGTCTGTCGGCTTCCCAGCGTCGGGCGGAGCTGCGTCGGAGAAAGCTGC GGTCCCAGCGGGCTCAGGTCTGTCGGCTTCCCGGCGTCGGGCGGAGCTGCGTCGGAGAAAGCTGC A G CAMLG Ensembl:ENSG00000164615 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:134738599..134738698 32194978 MeRIP-seq:(Medium) rs778378306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250339,Human_RBP_ID_631720,Human_RBP_ID_788308,Human_RBP_ID_946095,Human_RBP_ID_4809441,Human_RBP_ID_8894087,Human_RBP_ID_15302792 Human_Splice_Rec_693335,Human_Splice_Rec_693341 RMVar_hsa_circ_234594,RMVar_hsa_circ_118471 105312 RMVar_ID_105312 Human_SNP_ID_252331287 m1A Human chr5 - 134758901 134758901 134758901 CGACCGCGGGAATACTGGTGCCCTTGAGTACCACGCACAGGCGAACCGGACAAACAAGGAGGCTG CGACCGCGGGAATACTGGTGCCCTTGAGTACCTCGCACAGGCGAACCGGACAAACAAGGAGGCTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:134758801..134759009 26863410 MeRIP-seq:(Medium) rs373840799 Functional Loss SNV dbSNP153 33..33 33 - - - 105313 RMVar_ID_105313 Human_SNP_ID_252332632 m1A Human chr5 + 134763996 134763996 134763996 ACCCTCAGACAAAAGAAGTAAACGTGGAGATGACAGACGGTCTAGAAGTAGAGATAGAGATAGGA ACCCTCAGACAAAAGAAGTAAACGTGGAGATGTCAGACGGTCTAGAAGTAGAGATAGAGATAGGA A T DDX46 Ensembl:ENSG00000145833 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:134763976..134764000 26863196 MeRIP-seq:(Medium) rs148583666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78284,Human_RBP_ID_7385453,Human_RBP_ID_15303040,Human_RBP_ID_24083516,Human_RBP_ID_24547993,Human_RBP_ID_26351274 Human_Splice_Rec_693346,Human_Splice_Rec_693347,Human_Splice_Rec_693368,Human_Splice_Rec_693369,Human_Splice_Rec_693408,Human_Splice_Rec_693409,Human_Splice_Rec_693448,Human_Splice_Rec_693449 RMVar_hsa_circ_367645,RMVar_hsa_circ_364256 105314 RMVar_ID_105314 Human_SNP_ID_252335400 m1A Human chr5 + 134773764 134773764 134773764 AAGCGAAAAGAAAGAGTAGAAAAATGGCGAGAAGAGCAACGTAAAAAGGCTATGGAAAACATAGG AAGCGAAAAGAAAGAGTAGAAAAATGGCGAGAGGAGCAACGTAAAAAGGCTATGGAAAACATAGG A G DDX46 Ensembl:ENSG00000145833 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134758776..134777790 26863196 MeRIP-seq:(Medium) rs374470384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839951,Human_RBP_ID_2895502,Human_RBP_ID_3968142,Human_RBP_ID_7385480,Human_RBP_ID_15303156,Human_RBP_ID_18038845,Human_RBP_ID_22009559,Human_RBP_ID_24547995,Human_RBP_ID_24554378,Human_RBP_ID_26351278 Human_Splice_Rec_693350,Human_Splice_Rec_693351,Human_Splice_Rec_693372,Human_Splice_Rec_693373,Human_Splice_Rec_693414,Human_Splice_Rec_693415,Human_Splice_Rec_693454,Human_Splice_Rec_693455,Human_Splice_Rec_693489 RMVar_hsa_circ_55145,RMVar_hsa_circ_70760,RMVar_hsa_circ_367645,RMVar_hsa_circ_342231,RMVar_hsa_circ_355586,RMVar_hsa_circ_356628,RMVar_hsa_circ_71771,RMVar_hsa_circ_63579,RMVar_hsa_circ_67145,RMVar_hsa_circ_60426,RMVar_hsa_circ_234598 105315 RMVar_ID_105315 Human_SNP_ID_252354150 m1A Human chr5 - 134846100 134846100 134846100 CCCCAGCCCGCCGCCTCTGCACGGTGCGGAGAACGGGCCAAGACGGAGTGGCAGGCAGCGAGGGC CCCCAGCCCGCCGCCTCTGCACGGTGCGGAGATCGGGCCAAGACGGAGTGGCAGGCAGCGAGGGC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:134845999..134846180 26863410 MeRIP-seq:(Medium) rs887410017 Functional Loss SNV dbSNP153 33..33 33 - - - 105316 RMVar_ID_105316 Human_SNP_ID_252354181 m1A Human chr5 + 134846178 134846178 134846178 AGCACGAGGTTCCCAGCCGCTGGGAAGCCCCTAGACGCGCCGAGGGGCCGGGCTACGAGCGGCTG AGCACGAGGTTCCCAGCCGCTGGGAAGCCCCTCGACGCGCCGAGGGGCCGGGCTACGAGCGGCTG A C DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134846128..134846345 26863196 MeRIP-seq:(Medium) rs1363898881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1644920,Human_RBP_ID_4845360,Human_RBP_ID_8943845,Human_RBP_ID_18425005,Human_RBP_ID_26792123 Human_Splice_Rec_693549,Human_Splice_Rec_693551,Human_Splice_Rec_693555 RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 105317 RMVar_ID_105317 Human_SNP_ID_252354195 m1A Human chr5 - 134846224 134846224 134846224 ACCCCGCTCCCGGCCGGCTGACCAGCCCGCGCACCCCTACCTACCTCAGCCGCTCGTAGCCCGGC ACCCCGCTCCCGGCCGGCTGACCAGCCCGCGCTCCCCTACCTACCTCAGCCGCTCGTAGCCCGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134846216..134846353 26863196 MeRIP-seq:(Medium) rs1210195143 Functional Loss SNV dbSNP153 33..33 33 - - - 105318 RMVar_ID_105318 Human_SNP_ID_252361896 m1A Human chr5 - 134874482 134874482 134874482 GGGAAGTCCCAGCACCCACAGCAATACTTGCCACCAGCCGAGGAGCCGCATGACGCGGGGCGGTC GGGAAGTCCCAGCACCCACAGCAATACTTGCCCCCAGCCGAGGAGCCGCATGACGCGGGGCGGTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134874432..134874591 26863196 MeRIP-seq:(Medium) rs1373214166 Functional Loss SNV dbSNP153 33..33 33 - - - 105319 RMVar_ID_105319 Human_SNP_ID_252365308 m1A Human chr5 + 134887796 134887796 134887796 ACCTGGGTGAGGAGGAGCTCCTGCATGACCCGATGGGCCAGGACAGGGCAGCAGAAGAGGCCAAT ACCTGGGTGAGGAGGAGCTCCTGCATGACCCGTTGGGCCAGGACAGGGCAGCAGAAGAGGCCAAT A T TXNDC15 Ensembl:ENSG00000113621 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134887750..134887854 26863196 MeRIP-seq:(Medium) rs777340261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845364,Human_RBP_ID_15305855,Human_RBP_ID_18056869,Human_RBP_ID_22459248 Human_Splice_Rec_693578 RMVar_hsa_circ_17074,RMVar_hsa_circ_308237,RMVar_hsa_circ_234627 105320 RMVar_ID_105320 Human_SNP_ID_252365309 m1A Human chr5 - 134887797 134887797 134887797 CATTGGCCTCTTCTGCTGCCCTGTCCTGGCCCATCGGGTCATGCAGGAGCTCCTCCTCACCCAGG CATTGGCCTCTTCTGCTGCCCTGTCCTGGCCCGTCGGGTCATGCAGGAGCTCCTCCTCACCCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134887662..134887886 26863196 MeRIP-seq:(Medium) rs1038239896 Functional Loss SNV dbSNP153 33..33 33 - - - 105321 RMVar_ID_105321 Human_SNP_ID_252368304 m1A Human chr5 + 134900509 134900509 134900509 CAGCCTGGCCAACTTGGTGAAACCCTCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTG CAGCCTGGCCAACTTGGTGAAACCCTCTCTCTGCTAAAAATACAAAAAATTAGCTGGGCGTGGTG A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs959243835 Functional Loss SNV dbSNP153 33..33 33 - - - 105322 RMVar_ID_105322 Human_SNP_ID_252368327 m1A Human chr5 + 134900591 134900591 134900591 CAGCTACTTGGGAAAGCTGAGGCATGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGC CAGCTACTTGGGAAAGCTGAGGCATGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGC A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs909640297 Functional Loss SNV dbSNP153 33..33 33 - - - 105323 RMVar_ID_105323 Human_SNP_ID_252368408 m1A Human chr5 + 134900971 134900967 134900972 CATCACACCCAGCTAATTTTTCTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGG CATCACACCCAGCTAATTTTTCTATTTTT_____AGATGGGGTTTTGCCATGTTGGCCAGGCTGG TAGTAG T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs983033859 Functional Loss DEL dbSNP153 30..34 33 - - - 105324 RMVar_ID_105324 Human_SNP_ID_252368422 m1A Human chr5 + 134901040 134901040 134901040 AAACTGCTGACTTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAG AAACTGCTGACTTCAGGTGATCCACCCGCCTCCGCCTCCCAAAGTGTTGGGATTACAGGTGTGAG A C TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs908358564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_289699 105325 RMVar_ID_105325 Human_SNP_ID_252368425 m1A Human chr5 + 134901049 134901049 134901049 ACTTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGCGC ACTTCAGGTGATCCACCCGCCTCAGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCCACTGCGC A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs909596961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_289699 105326 RMVar_ID_105326 Human_SNP_ID_252374255 m1A Human chr5 + 134923884 134923884 134923884 GATCGATGAGAAGGCGGTTGAAGCGTCTGGTGAGTAGTGTATGGCTAGGAATAGTCCTGTGGTGA GATCGATGAGAAGGCGGTTGAAGCGTCTGGTGTGTAGTGTATGGCTAGGAATAGTCCTGTGGTGA A T PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134923875..134923995 26863196 MeRIP-seq:(Medium) rs1174071688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5242266,Human_RBP_ID_8236838,Human_RBP_ID_17159812 RMVar_hsa_circ_234628,RMVar_hsa_circ_76520,RMVar_hsa_circ_119817,RMVar_hsa_circ_324049,RMVar_hsa_circ_234629 105327 RMVar_ID_105327 Human_SNP_ID_252374383 m1A Human chr5 - 134924221 134924221 134924221 AGAATAATAACACACCCAATCACACCACTAACAATCAATACTAAACCCCCATAAATAGGAGAAGG AGAATAATAACACACCCAATCACACCACTAACGATCAATACTAAACCCCCATAAATAGGAGAAGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:134924127..134924251 26863410 MeRIP-seq:(Medium) rs530322605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2956607,Human_RBP_ID_17033187,Human_RBP_ID_18202092 105328 RMVar_ID_105328 Human_SNP_ID_252374386 m1A Human chr5 - 134924236 134924236 134924236 CCTCCCCCGTAATTCAGAATAATAACACACCCAATCACACCACTAACAATCAATACTAAACCCCC CCTCCCCCGTAATTCAGAATAATAACACACCCGATCACACCACTAACAATCAATACTAAACCCCC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:134924141..134924264 26863410 MeRIP-seq:(Medium) rs113212135 Functional Loss SNV dbSNP153 33..33 33 - - - 105329 RMVar_ID_105329 Human_SNP_ID_252374387 m1A Human chr5 - 134924236 134924236 134924236 CCTCCCCCGTAATTCAGAATAATAACACACCCAATCACACCACTAACAATCAATACTAAACCCCC CCTCCCCCGTAATTCAGAATAATAACACACCCCATCACACCACTAACAATCAATACTAAACCCCC T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:134924141..134924264 26863410 MeRIP-seq:(Medium) rs113212135 Functional Loss SNV dbSNP153 33..33 33 - - - 105330 RMVar_ID_105330 Human_SNP_ID_252374440 m1A Human chr5 - 134924408 134924408 134924408 CACCCATAACACTAATCCTACTTCCATCACCAACCCCACTAAAACACTTACCAAGACCTCAACCC CACCCATAACACTAATCCTACTTCCATCACCAGCCCCACTAAAACACTTACCAAGACCTCAACCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134924406..134924502 26863196 MeRIP-seq:(Medium) rs553350251 Functional Loss SNV dbSNP153 33..33 33 - - - 105331 RMVar_ID_105331 Human_SNP_ID_252374492 m1A Human chr5 - 134924576 134924576 134924576 AACAAACAATGTTCAACCAGTAACTACTACTAATCAACGCCCATAATCATACAAAGCCCCCGCAC AACAAACAATGTTCAACCAGTAACTACTACTATTCAACGCCCATAATCATACAAAGCCCCCGCAC T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:134924484..134924611 26863410 MeRIP-seq:(Medium) rs77382950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2956608,Human_RBP_ID_15306430,Human_RBP_ID_17038059,Human_RBP_ID_18210405,Human_RBP_ID_22827159,Human_RBP_ID_23050947,Human_RBP_ID_23191872,Human_RBP_ID_25857401,Human_RBP_ID_26521465,Human_RBP_ID_26699177 105332 RMVar_ID_105332 Human_SNP_ID_252374493 m1A Human chr5 - 134924576 134924576 134924576 AACAAACAATGTTCAACCAGTAACTACTACTAATCAACGCCCATAATCATACAAAGCCCCCGCAC AACAAACAATGTTCAACCAGTAACTACTACTAGTCAACGCCCATAATCATACAAAGCCCCCGCAC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:134924484..134924611 26863410 MeRIP-seq:(Medium) rs77382950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2956608,Human_RBP_ID_15306430,Human_RBP_ID_17038059,Human_RBP_ID_18210405,Human_RBP_ID_22827159,Human_RBP_ID_23050947,Human_RBP_ID_23191872,Human_RBP_ID_25857401,Human_RBP_ID_26521465,Human_RBP_ID_26699177 105333 RMVar_ID_105333 Human_SNP_ID_252374937 m1A Human chr5 - 134925692 134925692 134925692 CTACTCCACTCAAGCACTATAGTTGTAGCAGGAGTCTTCCTACTCATCCGCTTCCACCCCCTAGC CTACTCCACTCAAGCACTATAGTTGTAGCAGGGGTCTTCCTACTCATCCGCTTCCACCCCCTAGC T C MTND5P11 Ensembl:ENSG00000248923 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:134925676..134925750;chr5:134925601..134925736;chr5:134925651..134925737 26863196 MeRIP-seq:(Medium) rs77289145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22419805 Human_miRNA_ID_1907447 105334 RMVar_ID_105334 Human_SNP_ID_252375154 m1A Human chr5 + 134926274 134926274 134926274 GTTTGGGTTGTTGCCCAGTGTCAGTTTGAGATAATGACTTCTTGGTCTAGGTATATGAATATTGT GTTTGGGTTGTTGCCCAGTGTCAGTTTGAGATCATGACTTCTTGGTCTAGGTATATGAATATTGT A C PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:134926269..134926363 26863196 MeRIP-seq:(Medium) rs1296908926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234628,RMVar_hsa_circ_76520,RMVar_hsa_circ_119817,RMVar_hsa_circ_324049,RMVar_hsa_circ_234629 105335 RMVar_ID_105335 Human_SNP_ID_252375414 m1A Human chr5 - 134927077 134927077 134927077 ACCGGCGCAGTCATTCTCATAGTCGCCCACGGACTTACATCCTCATTACTATTCTGCCTAGCAAA ACCGGCGCAGTCATTCTCATAGTCGCCCACGGTCTTACATCCTCATTACTATTCTGCCTAGCAAA T A MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134927026..134927100 26863196 MeRIP-seq:(Medium) rs112820482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250560,Human_RBP_ID_283727,Human_RBP_ID_632013,Human_RBP_ID_789056,Human_RBP_ID_838888,Human_RBP_ID_945064,Human_RBP_ID_1064115,Human_RBP_ID_1141676,Human_RBP_ID_1210659,Human_RBP_ID_1244246,Human_RBP_ID_1319287,Human_RBP_ID_1390095,Human_RBP_ID_1645037,Human_RBP_ID_1987158,Human_RBP_ID_2895892,Human_RBP_ID_3758132,Human_RBP_ID_4847331,Human_RBP_ID_5090138,Human_RBP_ID_5214837,Human_RBP_ID_5267672,Human_RBP_ID_5427620,Human_RBP_ID_5476215,Human_RBP_ID_5510102,Human_RBP_ID_5641142,Human_RBP_ID_5656085,Human_RBP_ID_7386366,Human_RBP_ID_8132595,Human_RBP_ID_8214817,Human_RBP_ID_8267331,Human_RBP_ID_8603117,Human_RBP_ID_8730282,Human_RBP_ID_8884387,Human_RBP_ID_9169757,Human_RBP_ID_9262497,Human_RBP_ID_9304828,Human_RBP_ID_9341536,Human_RBP_ID_9437263,Human_RBP_ID_10231865,Human_RBP_ID_15306450,Human_RBP_ID_17033188,Human_RBP_ID_17090679,Human_RBP_ID_17160103,Human_RBP_ID_17196264,Human_RBP_ID_17209362,Human_RBP_ID_17297939,Human_RBP_ID_17411564,Human_RBP_ID_17527307,Human_RBP_ID_17575985,Human_RBP_ID_17584801,Human_RBP_ID_17631684,Human_RBP_ID_17671769,Human_RBP_ID_17673927,Human_RBP_ID_17706993,Human_RBP_ID_18039010,Human_RBP_ID_18170791,Human_RBP_ID_18202094,Human_RBP_ID_18210407,Human_RBP_ID_18353362,Human_RBP_ID_18409651,Human_RBP_ID_18448084,Human_RBP_ID_18502351,Human_RBP_ID_18518204,Human_RBP_ID_18538370,Human_RBP_ID_18544889,Human_RBP_ID_18832792,Human_RBP_ID_18927244,Human_RBP_ID_18956919,Human_RBP_ID_19128453,Human_RBP_ID_21120174,Human_RBP_ID_21960544,Human_RBP_ID_21990511,Human_RBP_ID_22365389,Human_RBP_ID_22372176,Human_RBP_ID_22404042,Human_RBP_ID_22425806,Human_RBP_ID_22511459,Human_RBP_ID_23292551,Human_RBP_ID_24385635,Human_RBP_ID_26699181,Human_RBP_ID_26750956,Human_RBP_ID_27160312,Human_RBP_ID_27331346,Human_RBP_ID_27511451,Human_RBP_ID_27734882 Human_miRNA_ID_1861377 105336 RMVar_ID_105336 Human_SNP_ID_252375415 m1A Human chr5 - 134927077 134927077 134927077 ACCGGCGCAGTCATTCTCATAGTCGCCCACGGACTTACATCCTCATTACTATTCTGCCTAGCAAA ACCGGCGCAGTCATTCTCATAGTCGCCCACGGGCTTACATCCTCATTACTATTCTGCCTAGCAAA T C MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:134927026..134927100 26863196 MeRIP-seq:(Medium) rs112820482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250560,Human_RBP_ID_283727,Human_RBP_ID_632013,Human_RBP_ID_789056,Human_RBP_ID_838888,Human_RBP_ID_945064,Human_RBP_ID_1064115,Human_RBP_ID_1141676,Human_RBP_ID_1210659,Human_RBP_ID_1244246,Human_RBP_ID_1319287,Human_RBP_ID_1390095,Human_RBP_ID_1645037,Human_RBP_ID_1987158,Human_RBP_ID_2895892,Human_RBP_ID_3758132,Human_RBP_ID_4847331,Human_RBP_ID_5090138,Human_RBP_ID_5214837,Human_RBP_ID_5267672,Human_RBP_ID_5427620,Human_RBP_ID_5476215,Human_RBP_ID_5510102,Human_RBP_ID_5641142,Human_RBP_ID_5656085,Human_RBP_ID_7386366,Human_RBP_ID_8132595,Human_RBP_ID_8214817,Human_RBP_ID_8267331,Human_RBP_ID_8603117,Human_RBP_ID_8730282,Human_RBP_ID_8884387,Human_RBP_ID_9169757,Human_RBP_ID_9262497,Human_RBP_ID_9304828,Human_RBP_ID_9341536,Human_RBP_ID_9437263,Human_RBP_ID_10231865,Human_RBP_ID_15306450,Human_RBP_ID_17033188,Human_RBP_ID_17090679,Human_RBP_ID_17160103,Human_RBP_ID_17196264,Human_RBP_ID_17209362,Human_RBP_ID_17297939,Human_RBP_ID_17411564,Human_RBP_ID_17527307,Human_RBP_ID_17575985,Human_RBP_ID_17584801,Human_RBP_ID_17631684,Human_RBP_ID_17671769,Human_RBP_ID_17673927,Human_RBP_ID_17706993,Human_RBP_ID_18039010,Human_RBP_ID_18170791,Human_RBP_ID_18202094,Human_RBP_ID_18210407,Human_RBP_ID_18353362,Human_RBP_ID_18409651,Human_RBP_ID_18448084,Human_RBP_ID_18502351,Human_RBP_ID_18518204,Human_RBP_ID_18538370,Human_RBP_ID_18544889,Human_RBP_ID_18832792,Human_RBP_ID_18927244,Human_RBP_ID_18956919,Human_RBP_ID_19128453,Human_RBP_ID_21120174,Human_RBP_ID_21960544,Human_RBP_ID_21990511,Human_RBP_ID_22365389,Human_RBP_ID_22372176,Human_RBP_ID_22404042,Human_RBP_ID_22425806,Human_RBP_ID_22511459,Human_RBP_ID_23292551,Human_RBP_ID_24385635,Human_RBP_ID_26699181,Human_RBP_ID_26750956,Human_RBP_ID_27160312,Human_RBP_ID_27331346,Human_RBP_ID_27511451,Human_RBP_ID_27734882 Human_miRNA_ID_1861377 105337 RMVar_ID_105337 Human_SNP_ID_252375661 m1A Human chr5 + 134927804 134927804 134927804 GTGGTTCATTGGATAAGTGGCGTTGGCTTGCCATGATTGTGAGGGGCAGGAGTCAGGTAGTTAGT GTGGTTCATTGGATAAGTGGCGTTGGCTTGCCGTGATTGTGAGGGGCAGGAGTCAGGTAGTTAGT A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:134927776..134927850 26863196 MeRIP-seq:(Medium) rs1383430039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17159831,Human_RBP_ID_17196270 RMVar_hsa_circ_234628,RMVar_hsa_circ_76520,RMVar_hsa_circ_119817,RMVar_hsa_circ_324049,RMVar_hsa_circ_234629 105338 RMVar_ID_105338 Human_SNP_ID_406697010 m1A Human chr9 - 91247445 91247445 91247445 TCCAAGGAGATGGAGAGGCTGGGAATTGAGGTACTGTAGGCGTGCAGCTGTGAGAGTGAGAAAAA TCCAAGGAGATGGAGAGGCTGGGAATTGAGGTTCTGTAGGCGTGCAGCTGTGAGAGTGAGAAAAA T A AUH Ensembl:ENSG00000148090 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:91247394..91247510 26863196 MeRIP-seq:(Medium) rs1450065224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16730070 105339 RMVar_ID_105339 Human_SNP_ID_406707556 m1A Human chr9 - 91292154 91292154 91292154 TGAAGAGGTGTTGTTTCTTCTATTCCTATGAAAAAAATAGATGAGCTTCTGTTCTTGAAAGAGCC TGAAGAGGTGTTGTTTCTTCTATTCCTATGAAGAAAATAGATGAGCTTCTGTTCTTGAAAGAGCC T C AUH Ensembl:ENSG00000148090 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:91292142..91292225 26863196 MeRIP-seq:(Medium) rs1302698736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734 105340 RMVar_ID_105340 Human_SNP_ID_406724026 m1A Human chr9 - 91361669 91361669 91361669 GAAAAGGGGCTACAGCTCTGAGATGAAGACGGAGGACGAGCTGCGGGTGCGGCACCTGGAGGAGG GAAAAGGGGCTACAGCTCTGAGATGAAGACGGCGGACGAGCTGCGGGTGCGGCACCTGGAGGAGG T G AUH Ensembl:ENSG00000148090 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:91360431..91361885 26863196 MeRIP-seq:(Medium) rs1319901161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963306,Human_RBP_ID_19025101,Human_RBP_ID_23094309,Human_RBP_ID_26360796 Human_Splice_Rec_1060339,Human_Splice_Rec_1060355,Human_Splice_Rec_1060377 105341 RMVar_ID_105341 Human_SNP_ID_406810313 m1A Human chr9 - 91723786 91723786 91723786 GGGCGCTGATGACACACAGAACGCCCCAGAAGATGGGGCCCAGAGCACCGTGCAGGAAGCAGAGG GGGCGCTGATGACACACAGAACGCCCCAGAAGTTGGGGCCCAGAGCACCGTGCAGGAAGCAGAGG T A ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:91723735..91723903 26863196 MeRIP-seq:(Medium) rs1305393719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97319,RMVar_hsa_circ_257746 105342 RMVar_ID_105342 Human_SNP_ID_406810314 m1A Human chr9 - 91723786 91723786 91723786 GGGCGCTGATGACACACAGAACGCCCCAGAAGATGGGGCCCAGAGCACCGTGCAGGAAGCAGAGG GGGCGCTGATGACACACAGAACGCCCCAGAAGGTGGGGCCCAGAGCACCGTGCAGGAAGCAGAGG T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:91723735..91723903 26863196 MeRIP-seq:(Medium) rs1305393719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97319,RMVar_hsa_circ_257746 105343 RMVar_ID_105343 Human_SNP_ID_406813127 m1A Human chr9 - 91733298 91733298 91733298 CCGGACACCCAAGCCGCGTGAGCTGTGCCGCGACGAGTGCGAGGTGCTGGAGAGCGACCTGTGCC CCGGACACCCAAGCCGCGTGAGCTGTGCCGCGGCGAGTGCGAGGTGCTGGAGAGCGACCTGTGCC T C ROR2 Ensembl:ENSG00000169071 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:91733247..91733391 26863196 MeRIP-seq:(Medium) rs760726459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18196901 RMVar_hsa_circ_50162 105344 RMVar_ID_105344 Human_SNP_ID_406825979 m1A Human chr9 - 91784099 91784099 91784099 ACGGGAGGCCGGGCTGTGGTGTGGACAGGTCAAGCATGGTGTCTCCTGGACATGCAAGTGGAGGT ACGGGAGGCCGGGCTGTGGTGTGGACAGGTCAGGCATGGTGTCTCCTGGACATGCAAGTGGAGGT T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:91783742..91784243 26863196 MeRIP-seq:(Medium) rs1041437594 Functional Loss SNV dbSNP153 33..33 33 - - - 105345 RMVar_ID_105345 Human_SNP_ID_406835265 m1A Human chr9 - 91819602 91819601 91819603 CAACACACACTCACTCAAAGACAGACAAACACAGACACACAGAACACTCAGAGACACACAGAATA CAACACACACTCACTCAAAGACAGACAAACA__GACACACAGAACACTCAGAGACACACAGAATA CTG C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:91819551..91819675 26863196 MeRIP-seq:(Medium) rs976448972 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_218845,Human_RBP_ID_268551,Human_RBP_ID_3224456,Human_RBP_ID_24537706 105346 RMVar_ID_105346 Human_SNP_ID_406835309 m1A Human chr9 - 91819681 91819676 91819682 CACAGAACACACTGAAAAACACACAAAGACAGATACACAGACACTGAAAGACACAGACACAGAGA CACAGAACACACTGAAAAACACACAAAGACA______CAGACACTGAAAGACACAGACACAGAGA GTGTATC G ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:91819629..91819775 26863196 MeRIP-seq:(Medium) rs146730403 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_15356,Human_RBP_ID_218846,Human_RBP_ID_3224456,Human_RBP_ID_24537514 105347 RMVar_ID_105347 Human_SNP_ID_406835361 m1A Human chr9 - 91819777 91819774 91819778 GGCACACACAGAACAAAGACACAGACATACACACAGAACACTGAGACACACACACAGAATATTGA GGCACACACAGAACAAAGACACAGACATACA____GAACACTGAGACACACACACAGAATATTGA CTGTG C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:91819763..91819892 26863196 MeRIP-seq:(Medium) rs1459600814 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_218849,Human_RBP_ID_3224471,Human_RBP_ID_24537708 105348 RMVar_ID_105348 Human_SNP_ID_406851990 m1A Human chr9 - 91886459 91886459 91886459 ACAGTCGGTGGTGTAAGCAGAGACCCTGGTGTAGACAGATCGCGGTGTGGGGAGGAAGCAAGTGG ACAGTCGGTGGTGTAAGCAGAGACCCTGGTGTCGACAGATCGCGGTGTGGGGAGGAAGCAAGTGG T G ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:91886410..91886601 26863196 MeRIP-seq:(Medium) rs1299701052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9442283,Human_RBP_ID_27843595 RMVar_hsa_circ_257749,RMVar_hsa_circ_322347,RMVar_hsa_circ_257748,RMVar_hsa_circ_297285 105349 RMVar_ID_105349 Human_SNP_ID_406853938 m1A Human chr9 - 91894119 91894119 91894119 AGAGGTGGGTGCTGGGAGAGTGACGGGGCTGGAGTTGGGGAGCAGGGACCAGTCACAAGGGCTGT AGAGGTGGGTGCTGGGAGAGTGACGGGGCTGGTGTTGGGGAGCAGGGACCAGTCACAAGGGCTGT T A ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:91894104..91894281 26863196 MeRIP-seq:(Medium) rs1438291884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226653,Human_RBP_ID_8160007,Human_RBP_ID_8944688,Human_RBP_ID_17579502,Human_RBP_ID_22732794,Human_RBP_ID_23300680 RMVar_hsa_circ_322347 105350 RMVar_ID_105350 Human_SNP_ID_406856725 m1A Human chr9 + 91905386 91905386 91905386 ACACCATACACACAAGACACACAACACATACCACACACACAGAGAGACAAAAACTATACAAATGT ACACCATACACACAAGACACACAACACATACCGCACACACAGAGAGACAAAAACTATACAAATGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:91905134..91905425 26863196 MeRIP-seq:(Medium) rs1429981614 Functional Loss SNV dbSNP153 33..33 33 - - - 105351 RMVar_ID_105351 Human_SNP_ID_406861333 m1A Human chr9 + 91922944 91922944 91922944 GGGCAGCCTGCCTCTCAAAGCCCTGTCCTCCAACAGACTCACTCTGCCTCACTTCTGCTGGGCAT GGGCAGCCTGCCTCTCAAAGCCCTGTCCTCCAGCAGACTCACTCTGCCTCACTTCTGCTGGGCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:91922806..91923003 26863196 MeRIP-seq:(Medium) rs1335481044 Functional Loss SNV dbSNP153 33..33 33 - - - 105352 RMVar_ID_105352 Human_SNP_ID_406862684 m1A Human chr9 - 91928113 91928113 91928113 AGAAGTTGGCTTGGCGTGTGAATGTAATGCAGAAGGTGGTGGCAGGTGAGTGTGATGCAGGAGGT AGAAGTTGGCTTGGCGTGTGAATGTAATGCAGCAGGTGGTGGCAGGTGAGTGTGATGCAGGAGGT T G ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:91928111..91928312 26863196 MeRIP-seq:(Medium) rs1161839549 Functional Loss SNV dbSNP153 33..33 33 - - - 105353 RMVar_ID_105353 Human_SNP_ID_406868257 m1A Human chr9 + 91950077 91950077 91950077 GCGTCCGCTCCTCCTTCTCCCTGGCGCTTCGCAAACGGGTCCACTTCGAGGACCTCGTCGTCGTC GCGTCCGCTCCTCCTTCTCCCTGGCGCTTCGCCAACGGGTCCACTTCGAGGACCTCGTCGTCGTC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr9:91950026..91950225;chr9:91950026..91950194 26863196 MeRIP-seq:(Medium) rs1395764839 Functional Loss SNV dbSNP153 33..33 33 - - - 105354 RMVar_ID_105354 Human_SNP_ID_406888088 m1A Human chr9 + 92034157 92034157 92034157 GACACACACACTTCTCTAGTTTTGGTGTAGACATCGCCTGCTCTCAAAAGCCTGAGCAATGCCCC GACACACACACTTCTCTAGTTTTGGTGTAGACGTCGCCTGCTCTCAAAAGCCTGAGCAATGCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:92034031..92034386 26863196 MeRIP-seq:(Medium) rs550285546 Functional Loss SNV dbSNP153 33..33 33 - - - 105355 RMVar_ID_105355 Human_SNP_ID_406890185 m1A Human chr9 + 92043498 92043498 92043498 GGCTTAACATAACCACTGCTGACCTTCCCCAGAAGGTATTTCTCCACAGTTCTGTCCCTCTCACT GGCTTAACATAACCACTGCTGACCTTCCCCAGCAGGTATTTCTCCACAGTTCTGTCCCTCTCACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:92043494..92043606 26863196 MeRIP-seq:(Medium) rs1286937099 Functional Loss SNV dbSNP153 33..33 33 - - - 105356 RMVar_ID_105356 Human_SNP_ID_406897583 m1A Human chr9 - 92074559 92074559 92074559 CAGGATAAGGGTGGCCATGTTTCAATGGGATGATAAGGGGTGAATGATCAGTTGCAGGCGAAGGA CAGGATAAGGGTGGCCATGTTTCAATGGGATGTTAAGGGGTGAATGATCAGTTGCAGGCGAAGGA T A SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:92074534..92074650 26863196 MeRIP-seq:(Medium) rs1222507348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24312835 RMVar_hsa_circ_102678,RMVar_hsa_circ_106687,RMVar_hsa_circ_104282,RMVar_hsa_circ_257750,RMVar_hsa_circ_257751,RMVar_hsa_circ_306309,RMVar_hsa_circ_257753,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_257758,RMVar_hsa_circ_328408,RMVar_hsa_circ_90440,RMVar_hsa_circ_257759,RMVar_hsa_circ_322947 105357 RMVar_ID_105357 Human_SNP_ID_406898017 m1A Human chr9 - 92076416 92076416 92076416 CAGAAGGAGAGTAATAGGAGTGATAGATGAGAAGGAGAAATATTGGCCACTGGGAGCAGATACTG CAGAAGGAGAGTAATAGGAGTGATAGATGAGAGGGAGAAATATTGGCCACTGGGAGCAGATACTG T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:92076398..92076737 26863196 MeRIP-seq:(Medium) rs1411283825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102678,RMVar_hsa_circ_106687,RMVar_hsa_circ_104282,RMVar_hsa_circ_257750,RMVar_hsa_circ_257751,RMVar_hsa_circ_306309,RMVar_hsa_circ_257753,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_257758,RMVar_hsa_circ_328408,RMVar_hsa_circ_90440,RMVar_hsa_circ_257759,RMVar_hsa_circ_322947 105358 RMVar_ID_105358 Human_SNP_ID_406905526 m1A Human chr9 - 92105637 92105637 92105637 GCGCTCCTCACTGCCCAGACGGTGCGGTGGCCAGGCAGAGGCGCTCCTCACTTCCCAGATGGTGG GCGCTCCTCACTGCCCAGACGGTGCGGTGGCCGGGCAGAGGCGCTCCTCACTTCCCAGATGGTGG T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:92105588..92105906 26863196 MeRIP-seq:(Medium) rs1401812726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102678,RMVar_hsa_circ_106687,RMVar_hsa_circ_257750,RMVar_hsa_circ_257751,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_287137,RMVar_hsa_circ_349406 105359 RMVar_ID_105359 Human_SNP_ID_406930524 m1A Human chr9 + 92210792 92210792 92210792 AGGTGTAATTAGGGAAGGGCTGACCGAACAACATTGATAAGTACATGCTAGAAGTCTGCTGTTGT AGGTGTAATTAGGGAAGGGCTGACCGAACAACGTTGATAAGTACATGCTAGAAGTCTGCTGTTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:92210742..92210830 26863196 MeRIP-seq:(Medium) rs534901468 Functional Loss SNV dbSNP153 33..33 33 - - - 105360 RMVar_ID_105360 Human_SNP_ID_406939666 m1A Human chr9 - 92245073 92245073 92245073 GAAGCTGATTAACAGTGTAGCTGCTTCTCCATAGGGACCATTGTTGTGGAAGGCCATGAATTGCA GAAGCTGATTAACAGTGTAGCTGCTTCTCCATTGGGACCATTGTTGTGGAAGGCCATGAATTGCA T A IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr9:92245031..92245122;chr9:92244951..92250286 26863196,32194978 MeRIP-seq:(Medium) rs113396633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5043908 RMVar_hsa_circ_32472,RMVar_hsa_circ_92786,RMVar_hsa_circ_280674,RMVar_hsa_circ_375886,RMVar_hsa_circ_345342,RMVar_hsa_circ_110631,RMVar_hsa_circ_46434,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_41218,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_257767,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,RMVar_hsa_circ_50727,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_257770,RMVar_hsa_circ_365044,RMVar_hsa_circ_314649,RMVar_hsa_circ_46513,RMVar_hsa_circ_257774,RMVar_hsa_circ_30506,RMVar_hsa_circ_21654,RMVar_hsa_circ_115436,RMVar_hsa_circ_257773,RMVar_hsa_circ_103565,RMVar_hsa_circ_70139,RMVar_hsa_circ_125343,RMVar_hsa_circ_257776,RMVar_hsa_circ_257777,RMVar_hsa_circ_109384,RMVar_hsa_circ_257778,RMVar_hsa_circ_257779 105361 RMVar_ID_105361 Human_SNP_ID_406941114 m1A Human chr9 - 92250788 92250787 92250788 TTTTCTCACTGAATTGATGTACCAGAATCTAAAGGTGCTGATTGACCCTGTTTCTGTTCAGGACA TTTTCTCACTGAATTGATGTACCAGAATCTAA_GGTGCTGATTGACCCTGTTTCTGTTCAGGACA CT C IARS1 Ensembl:ENSG00000196305 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs753895682 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_721921,Human_RBP_ID_1339837,Human_RBP_ID_1707177,Human_RBP_ID_2066625,Human_RBP_ID_8929504,Human_RBP_ID_9239113,Human_RBP_ID_9264603,Human_RBP_ID_16733968,Human_RBP_ID_17322937,Human_RBP_ID_18911540,Human_RBP_ID_22838986,Human_RBP_ID_27138933,Human_RBP_ID_27547230 Human_Splice_Rec_1060822,Human_Splice_Rec_1060823,Human_Splice_Rec_1060888,Human_Splice_Rec_1060889,Human_Splice_Rec_1060956,Human_Splice_Rec_1060957,Human_Splice_Rec_1061020,Human_Splice_Rec_1061021,Human_Splice_Rec_1061059 RMVar_hsa_circ_32472,RMVar_hsa_circ_92786,RMVar_hsa_circ_280674,RMVar_hsa_circ_345342,RMVar_hsa_circ_110631,RMVar_hsa_circ_46434,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_26951,RMVar_hsa_circ_41218,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_257767,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,RMVar_hsa_circ_50727,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_257770,RMVar_hsa_circ_365044,RMVar_hsa_circ_46513,RMVar_hsa_circ_30506,RMVar_hsa_circ_21654,RMVar_hsa_circ_115436,RMVar_hsa_circ_257773,RMVar_hsa_circ_103565,RMVar_hsa_circ_70139,RMVar_hsa_circ_125343,RMVar_hsa_circ_257776,RMVar_hsa_circ_257777,RMVar_hsa_circ_109384,RMVar_hsa_circ_56996,RMVar_hsa_circ_257778,RMVar_hsa_circ_257779,RMVar_hsa_circ_87454,RMVar_hsa_circ_293518,RMVar_hsa_circ_257781,RMVar_hsa_circ_52301,RMVar_hsa_circ_330216,RMVar_hsa_circ_257780,RMVar_hsa_circ_326119,RMVar_hsa_circ_92259,RMVar_hsa_circ_114960,RMVar_hsa_circ_81681,RMVar_hsa_circ_257782,RMVar_hsa_circ_338099,RMVar_hsa_circ_257783,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257786 105362 RMVar_ID_105362 Human_SNP_ID_406944920 m1A Human chr9 + 92265552 92265552 92265552 CTTCAAGTTCCGCCACTGACCCAATGCATACCACCTGTCAAAAACAAAGTTCAATAGCAGGAGCT CTTCAAGTTCCGCCACTGACCCAATGCATACCGCCTGTCAAAAACAAAGTTCAATAGCAGGAGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:92265501..92265603 26863196 MeRIP-seq:(Medium) rs1426262068 Functional Loss SNV dbSNP153 33..33 33 - - - 105363 RMVar_ID_105363 Human_SNP_ID_406945896 m1A Human chr9 - 92269830 92269830 92269830 TCATAGTGTCTTTTGTCATGTGGTTAGTAAGTATGGTTTACACTTCCCCCAAGTTATAATTTTAA TCATAGTGTCTTTTGTCATGTGGTTAGTAAGTGTGGTTTACACTTCCCCCAAGTTATAATTTTAA T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:92269827..92269959 26863196 MeRIP-seq:(Medium) rs912362384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17643105 RMVar_hsa_circ_32472,RMVar_hsa_circ_92786,RMVar_hsa_circ_280674,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_77221,RMVar_hsa_circ_3835,RMVar_hsa_circ_26951,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_365044,RMVar_hsa_circ_30506,RMVar_hsa_circ_257773,RMVar_hsa_circ_103565,RMVar_hsa_circ_257777,RMVar_hsa_circ_56996,RMVar_hsa_circ_87454,RMVar_hsa_circ_257781,RMVar_hsa_circ_52301,RMVar_hsa_circ_47473,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787,RMVar_hsa_circ_273589,RMVar_hsa_circ_290506,RMVar_hsa_circ_359241,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_257793,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_257795,RMVar_hsa_circ_63220,RMVar_hsa_circ_30110,RMVar_hsa_circ_257798,RMVar_hsa_circ_283495,RMVar_hsa_circ_362691,RMVar_hsa_circ_8235,RMVar_hsa_circ_305132,RMVar_hsa_circ_257801,RMVar_hsa_circ_48920,RMVar_hsa_circ_35600,RMVar_hsa_circ_313364,RMVar_hsa_circ_339542,RMVar_hsa_circ_3342,RMVar_hsa_circ_325678,RMVar_hsa_circ_276951,RMVar_hsa_circ_257803,RMVar_hsa_circ_257804,RMVar_hsa_circ_257802 105364 RMVar_ID_105364 Human_SNP_ID_406952158 m1A Human chr9 - 92293656 92293656 92293656 GTTGCAGCGTGGACGCCGGATGAGTTGCTTTTAGGCTTGCTGGCCCGCGGGGCTGTCCAGGCACG GTTGCAGCGTGGACGCCGGATGAGTTGCTTTTCGGCTTGCTGGCCCGCGGGGCTGTCCAGGCACG T G IARS1 Ensembl:ENSG00000196305 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:92293526..92293700 26863196 MeRIP-seq:(Medium) rs1016269384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92704,Human_RBP_ID_185505,Human_RBP_ID_1228013,Human_RBP_ID_1707497,Human_RBP_ID_5034102,Human_RBP_ID_7946608,Human_RBP_ID_8930097,Human_RBP_ID_9264634,Human_RBP_ID_9315139,Human_RBP_ID_16735840,Human_RBP_ID_18911722,Human_RBP_ID_22118738,Human_RBP_ID_22466153,Human_RBP_ID_23216502,Human_RBP_ID_24313156,Human_RBP_ID_26360385 Human_Splice_Rec_1060845,Human_Splice_Rec_1060913,Human_Splice_Rec_1060979,Human_Splice_Rec_1061065,Human_Splice_Rec_1061089 105365 RMVar_ID_105365 Human_SNP_ID_407033629 m1A Human chr9 + 92640159 92640159 92640159 GTGATCATGAGGCTACAACTGGGACTGAGGTGATGACAAGGGGGACCCCAGAGGATACATGTCTA GTGATCATGAGGCTACAACTGGGACTGAGGTGTTGACAAGGGGGACCCCAGAGGATACATGTCTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:92640156..92640260 26863196 MeRIP-seq:(Medium) rs1408592022 Functional Loss SNV dbSNP153 33..33 33 - - - 105366 RMVar_ID_105366 Human_SNP_ID_407033630 m1A Human chr9 + 92640171 92640171 92640171 CTACAACTGGGACTGAGGTGATGACAAGGGGGACCCCAGAGGATACATGTCTAACAGGGACCCGG CTACAACTGGGACTGAGGTGATGACAAGGGGGGCCCCAGAGGATACATGTCTAACAGGGACCCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:92640155..92640288 26863196 MeRIP-seq:(Medium) rs956158925 Functional Loss SNV dbSNP153 33..33 33 - - - 105367 RMVar_ID_105367 Human_SNP_ID_407040665 m1A Human chr9 + 92669671 92669671 92669671 GGGAATACTGAGGGGACGACAGACCGGCCAGGAGAAGGATCTGGGGCAATGGGAGACTGACCCAG GGGAATACTGAGGGGACGACAGACCGGCCAGGGGAAGGATCTGGGGCAATGGGAGACTGACCCAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:92669663..92669876 26863196 MeRIP-seq:(Medium) rs1034724566 Functional Loss SNV dbSNP153 33..33 33 - - - 105368 RMVar_ID_105368 Human_SNP_ID_407040791 m1A Human chr9 - 92669959 92669959 92669959 GGCATGGAAGAGGGGAAGATGGACGAGAATGAATGGGGGTACCACGGAGAGGGCAATAAGAGCCT GGCATGGAAGAGGGGAAGATGGACGAGAATGAGTGGGGGTACCACGGAGAGGGCAATAAGAGCCT T C IPPK Ensembl:ENSG00000127080 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:92669840..92670096 26863196 MeRIP-seq:(Medium) rs1392033775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037413,Human_RBP_ID_5634279,Human_RBP_ID_24313501 Human_Splice_Rec_1061707 105369 RMVar_ID_105369 Human_SNP_ID_407040805 m1A Human chr9 + 92669993 92669993 92669993 CATTCTCGTCCATCTTCCCCTCTTCCATGCCCAGGCGCAGCCCTGGCGCCTCGCGGGCTAGGACT CATTCTCGTCCATCTTCCCCTCTTCCATGCCCGGGCGCAGCCCTGGCGCCTCGCGGGCTAGGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:92669945..92670103 26863196 MeRIP-seq:(Medium) rs754739836 Functional Loss SNV dbSNP153 33..33 33 - - - 105370 RMVar_ID_105370 Human_SNP_ID_407051019 m1A Human chr9 + 92713107 92713107 92713107 ATTAAGGAAGCAAATATAATATCAAAATATCAAAAGTGCACAGGTTGATCGGATAAAAAAAGAAC ATTAAGGAAGCAAATATAATATCAAAATATCACAAGTGCACAGGTTGATCGGATAAAAAAAGAAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:92712856..92713106 32194978 MeRIP-seq:(Medium) rs912879981 Functional Loss SNV dbSNP153 33..33 33 - - - 105371 RMVar_ID_105371 Human_SNP_ID_407051691 m1A Human chr9 + 92715448 92715448 92715448 GCCAGCTGCCGCTGCATCTCATCCAGCTGTGTAATGTACTCGTCACACCTGTGGGTACCAAAAAC GCCAGCTGCCGCTGCATCTCATCCAGCTGTGTGATGTACTCGTCACACCTGTGGGTACCAAAAAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:92715397..92717831 32194978 MeRIP-seq:(Medium) rs140883066 Functional Loss SNV dbSNP153 33..33 33 - - - 105372 RMVar_ID_105372 Human_SNP_ID_407052338 m1A Human chr9 + 92717931 92717931 92717931 TTCTCATTCTCATACTTGCTCTTCAGGTTGGCAAGGGCCACCTCGGCCGTCTGGGGGACAGATGT TTCTCATTCTCATACTTGCTCTTCAGGTTGGCGAGGGCCACCTCGGCCGTCTGGGGGACAGATGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:92715198..92717930 32194978 MeRIP-seq:(Medium) rs1276406540 Functional Loss SNV dbSNP153 33..33 33 - - - 105373 RMVar_ID_105373 Human_SNP_ID_407052675 m1A Human chr9 - 92718887 92718887 92718887 GAGGCGCGTGGCCGGCGCTCACCCATCCTCCTACCCAAGGGGCTGCTGGCTCCTGAGGCGGGCCG GAGGCGCGTGGCCGGCGCTCACCCATCCTCCTGCCCAAGGGGCTGCTGGCTCCTGAGGCGGGCCG T C BICD2 Ensembl:ENSG00000185963 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:92718819..92718906 26863410 MeRIP-seq:(Medium) rs540475126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27547322 RMVar_hsa_circ_19386,RMVar_hsa_circ_31778 105374 RMVar_ID_105374 Human_SNP_ID_407052823 m1A Human chr9 - 92719205 92719205 92719205 GAGAAGGGCCGCTATGAGGCTGAGGGCCAGGCACTCACGGAGAAGGTCTCCCTGCTAGAGAAGGC GAGAAGGGCCGCTATGAGGCTGAGGGCCAGGCTCTCACGGAGAAGGTCTCCCTGCTAGAGAAGGC T A BICD2 Ensembl:ENSG00000185963 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:92719155..92719363 26863196 MeRIP-seq:(Medium) rs201784829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18911887 RMVar_hsa_circ_19386,RMVar_hsa_circ_31778 105375 RMVar_ID_105375 Human_SNP_ID_407064393 m1A Human chr9 + 92764753 92764753 92764753 CTCCTCCTCCGACGGCGCCGACATGGTGGCCGAGGGCTGAGCCGGCTCCCACTGAGGCTCTCGCA CTCCTCCTCCGACGGCGCCGACATGGTGGCCGGGGGCTGAGCCGGCTCCCACTGAGGCTCTCGCA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:92764596..92764805 26863410 MeRIP-seq:(Medium) rs1370426367 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 105376 RMVar_ID_105376 Human_SNP_ID_407064431 m1A Human chr9 + 92764801 92764801 92764801 CCACTGAGGCTCTCGCAGGCCGGGCCCTCCTCAGCCGCCGCCGCTGCCGCCGCCGCCGCCGCCCT CCACTGAGGCTCTCGCAGGCCGGGCCCTCCTCCGCCGCCGCCGCTGCCGCCGCCGCCGCCGCCCT A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:92764737..92764857 26863410 MeRIP-seq:(Medium) rs1409824009 Functional Loss SNV dbSNP153 33..33 33 - - - 105377 RMVar_ID_105377 Human_SNP_ID_407064432 m1A Human chr9 + 92764801 92764801 92764801 CCACTGAGGCTCTCGCAGGCCGGGCCCTCCTCAGCCGCCGCCGCTGCCGCCGCCGCCGCCGCCCT CCACTGAGGCTCTCGCAGGCCGGGCCCTCCTCGGCCGCCGCCGCTGCCGCCGCCGCCGCCGCCCT A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:92764737..92764857 26863410 MeRIP-seq:(Medium) rs1409824009 Functional Loss SNV dbSNP153 33..33 33 - - - 105378 RMVar_ID_105378 Human_SNP_ID_407064465 m1A Human chr9 + 92764840 92764840 92764840 GCCGCTGCCGCCGCCGCCGCCGCCCTGCCCCGACGGCCGCCCGCCCGCCCGCGCCGCCGCACGGC GCCGCTGCCGCCGCCGCCGCCGCCCTGCCCCGTCGGCCGCCCGCCCGCCCGCGCCGCCGCACGGC A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:92764743..92764862 26863410 MeRIP-seq:(Medium) rs13294942 Functional Loss SNV dbSNP153 33..33 33 - - - 105379 RMVar_ID_105379 Human_SNP_ID_407075115 m1A Human chr9 - 92809507 92809507 92809507 AGATCCACCCCCAAACCCGCGATCCACCCCCAAATCCAAGATCCACCACCAAACCCGCGATGTAG AGATCCACCCCCAAACCCGCGATCCACCCCCAGATCCAAGATCCACCACCAAACCCGCGATGTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:92809466..92809553 26863196 MeRIP-seq:(Medium) rs1455311926 Functional Loss SNV dbSNP153 33..33 33 - - - 105380 RMVar_ID_105380 Human_SNP_ID_407148988 m1A Human chr9 + 93111924 93111924 93111924 CACAGAGCTAGACTCGGGCAGCCAGAGCGGCGAGCTGAGTAACAGGGGTAACACCTCCCTGCTGC CACAGAGCTAGACTCGGGCAGCCAGAGCGGCGGGCTGAGTAACAGGGGTAACACCTCCCTGCTGC A G CARD19 Ensembl:ENSG00000165233 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:93111835..93111935 32194978 MeRIP-seq:(Medium) rs1242837002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062132,Human_Splice_Rec_1062133,Human_Splice_Rec_1062166,Human_Splice_Rec_1062167 RMVar_hsa_circ_27335,RMVar_hsa_circ_88575,RMVar_hsa_circ_257844 105381 RMVar_ID_105381 Human_SNP_ID_407152055 m1A Human chr9 + 93121638 93121638 93121638 TATATACAAGGTCTACGGCCCTCACAGGCCTGACTGGCTCCCTCTTGATGGCCACCAAGCCCAGG TATATACAAGGTCTACGGCCCTCACAGGCCTGTCTGGCTCCCTCTTGATGGCCACCAAGCCCAGG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:93121588..93121739 32194978 MeRIP-seq:(Medium) rs1232994958 Functional Loss SNV dbSNP153 33..33 33 - - - 105382 RMVar_ID_105382 Human_SNP_ID_407152100 m1A Human chr9 - 93121855 93121855 93121855 CTGGATGAGTGACCAGGGCCAGCCTCTGTCTCAGGACATTCCAGAAGGACAAGGAGATGTCTCTC CTGGATGAGTGACCAGGGCCAGCCTCTGTCTCGGGACATTCCAGAAGGACAAGGAGATGTCTCTC T C NINJ1 Ensembl:ENSG00000131669 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:93121588..93122188 32194978 MeRIP-seq:(Medium) rs1022740476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_722116,Human_RBP_ID_5124366,Human_RBP_ID_17550692,Human_RBP_ID_27570769 105383 RMVar_ID_105383 Human_SNP_ID_407152177 m1A Human chr9 + 93122157 93122157 93122157 CTCTGGCAGTCTGGGTAGTGCCATGTGCAGGGAGGTGGACACCTCACAGGTATGGCGACTCCTGG CTCTGGCAGTCTGGGTAGTGCCATGTGCAGGGGGGTGGACACCTCACAGGTATGGCGACTCCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93122107..93122180 26863196 MeRIP-seq:(Medium) rs534890359 Functional Loss SNV dbSNP153 33..33 33 - - - 105384 RMVar_ID_105384 Human_SNP_ID_407154837 m1A Human chr9 + 93132390 93132390 93132390 CCCCTCCCATCGGCCTGGCTTCCCATCCCCCCACCTCCTACCTGGCCCTCATGTGCTCTGTGGTC CCCCTCCCATCGGCCTGGCTTCCCATCCCCCCCCCTCCTACCTGGCCCTCATGTGCTCTGTGGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:93132384..93132717 26863196 MeRIP-seq:(Medium) rs1554756179 Functional Loss SNV dbSNP153 33..33 33 - - - 105385 RMVar_ID_105385 Human_SNP_ID_407154850 m1A Human chr9 + 93132445 93132445 93132445 CTCTGTGGTCCAGCCTCTGAGCCTTTGCTCCCACTGTTCCCTCTGCCTAGATGCCCTTCCACACA CTCTGTGGTCCAGCCTCTGAGCCTTTGCTCCCGCTGTTCCCTCTGCCTAGATGCCCTTCCACACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93132430..93132717 26863196 MeRIP-seq:(Medium) rs1375038033 Functional Loss SNV dbSNP153 33..33 33 - - - 105386 RMVar_ID_105386 Human_SNP_ID_407168554 m1A Human chr9 + 93185256 93185256 93185256 GCAGCGCTGGTAGCGCAGCCGGGAGCCCCCGGAGCCCCCGCGGACGCCGGCCCCGAGCCCGTGGG GCAGCGCTGGTAGCGCAGCCGGGAGCCCCCGGGGCCCCCGCGGACGCCGGCCCCGAGCCCGTGGG A G WNK2 Ensembl:ENSG00000165238 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93185215..93185485 26863196 MeRIP-seq:(Medium) rs967603088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5534783 RMVar_hsa_circ_123428,RMVar_hsa_circ_257849 105387 RMVar_ID_105387 Human_SNP_ID_407168607 m1A Human chr9 - 93185381 93185381 93185381 TCGCCTCGGCCGCCCCCTCATCCTCCTTCCTCACGGTCGCCGCCGCCTCCTCCCTGGGGCCGCCG TCGCCTCGGCCGCCCCCTCATCCTCCTTCCTCTCGGTCGCCGCCGCCTCCTCCCTGGGGCCGCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:93185333..93185454 26863196 MeRIP-seq:(Medium) rs1311582721 Functional Loss SNV dbSNP153 33..33 33 - - - 105388 RMVar_ID_105388 Human_SNP_ID_407188117 m1A Human chr9 + 93259004 93259004 93259004 GGGAATCGACGGCCTCCCTCCGGCCCTCCCAGACCTGCCGACCGCGACTGTGCCTCCCGTGCCAC GGGAATCGACGGCCTCCCTCCGGCCCTCCCAGCCCTGCCGACCGCGACTGTGCCTCCCGTGCCAC A C WNK2 Ensembl:ENSG00000165238 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93258899..93259081 26863196 MeRIP-seq:(Medium) rs1451097424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062226,Human_Splice_Rec_1062246,Human_Splice_Rec_1062294,Human_Splice_Rec_1062352,Human_Splice_Rec_1062408,Human_Splice_Rec_1062458,Human_Splice_Rec_1062490 105389 RMVar_ID_105389 Human_SNP_ID_407188303 m1A Human chr9 + 93259404 93259404 93259404 CCGGCACTGCCTCCACAACCCACACTGCCCCCACAACCCGTGCTGCCCCCGCAACCCACGCTGCC CCGGCACTGCCTCCACAACCCACACTGCCCCCGCAACCCGTGCTGCCCCCGCAACCCACGCTGCC A G WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93252934..93261958 26863196 MeRIP-seq:(Medium) rs147037304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135475,Human_RBP_ID_17094640,Human_RBP_ID_18962102 Human_miRNA_ID_1421805 105390 RMVar_ID_105390 Human_SNP_ID_407188338 m1A Human chr9 + 93259443 93259443 93259443 GTGCTGCCCCCGCAACCCACGCTGCCCCCTCAACCTGTGTTGCCCCCGCAACCCACACGGCCCCC GTGCTGCCCCCGCAACCCACGCTGCCCCCTCAGCCTGTGTTGCCCCCGCAACCCACACGGCCCCC A G WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93259393..93259524 26863196 MeRIP-seq:(Medium) rs1424706905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135259,Human_RBP_ID_17094640,Human_RBP_ID_18962102 105391 RMVar_ID_105391 Human_SNP_ID_407188343 m1A Human chr9 + 93259467 93259450 93259468 CCCCCTCAACCTGTGTTGCCCCCGCAACCCACACGGCCCCCTCAACCTGTGCTGCCCCCGCAACC CCCCCTCAACCTGTGT__________________GGCCCCCTCAACCTGTGCTGCCCCCGCAACC TTGCCCCCGCAACCCACAC T WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:93259378..93259538 26863196 MeRIP-seq:(Medium) rs778028677 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_5135259,Human_RBP_ID_18962102 105392 RMVar_ID_105392 Human_SNP_ID_407188361 m1A Human chr9 + 93259467 93259467 93259467 CCCCCTCAACCTGTGTTGCCCCCGCAACCCACACGGCCCCCTCAACCTGTGCTGCCCCCGCAACC CCCCCTCAACCTGTGTTGCCCCCGCAACCCACGCGGCCCCCTCAACCTGTGCTGCCCCCGCAACC A G WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:93259378..93259538 26863196 MeRIP-seq:(Medium) rs10124322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135259,Human_RBP_ID_18962102 105393 RMVar_ID_105393 Human_SNP_ID_407190692 m1A Human chr9 + 93267868 93267868 93267868 GAGGACACAGACGCCGACCGTGGCTCCGACCCAGGGACCAGCCCGCCACACCTCAGCACCTGCGG GAGGACACAGACGCCGACCGTGGCTCCGACCCGGGGACCAGCCCGCCACACCTCAGCACCTGCGG A G WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93267818..93268000 26863196 MeRIP-seq:(Medium) rs1252218621 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22119650 Human_Splice_Rec_1062257,Human_Splice_Rec_1062305,Human_Splice_Rec_1062363,Human_Splice_Rec_1062419,Human_Splice_Rec_1062469,Human_Splice_Rec_1062497,Human_Splice_Rec_1062501 RMVar_hsa_circ_104038,RMVar_hsa_circ_257852 105394 RMVar_ID_105394 Human_SNP_ID_407190979 m1A Human chr9 - 93268700 93268700 93268700 GGCGGCAGGGAGCTTAGAGGAAGTGGGGGCGAAGATTCAGGGGCCTCGGGGGCGGGGTGCTCAGC GGCGGCAGGGAGCTTAGAGGAAGTGGGGGCGAGGATTCAGGGGCCTCGGGGGCGGGGTGCTCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93267856..93268721 26863196 MeRIP-seq:(Medium) rs973592872 Functional Loss SNV dbSNP153 33..33 33 - - - 105395 RMVar_ID_105395 Human_SNP_ID_407195707 m1A Human chr9 + 93288891 93288891 93288891 AGCCAGGCGGGCCCCAGCAACCCTCCTGGGGCACCCCCAGCCCCTTTGGCCCCCTCCTCCCCTCC AGCCAGGCGGGCCCCAGCAACCCTCCTGGGGCCCCCCCAGCCCCTTTGGCCCCCTCCTCCCCTCC A C WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93288850..93288951 26863196 MeRIP-seq:(Medium) rs763004405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2684320 RMVar_hsa_circ_112391,RMVar_hsa_circ_36275,RMVar_hsa_circ_257854 105396 RMVar_ID_105396 Human_SNP_ID_407195870 m1A Human chr9 - 93289245 93289245 93289245 CTGACGGCCCCCACTGCGGCAGGAAGCAGGGGAGCAGGTTGACCCAAGGCGGGCTGTGGGGTCCC CTGACGGCCCCCACTGCGGCAGGAAGCAGGGGTGCAGGTTGACCCAAGGCGGGCTGTGGGGTCCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93289200..93289401 26863196 MeRIP-seq:(Medium) rs1250075819 Functional Loss SNV dbSNP153 33..33 33 - - - 105397 RMVar_ID_105397 Human_SNP_ID_407200010 m1A Human chr9 - 93302557 93302557 93302557 TTCACAGAGGCCAGGATCCTTCTATATTTCAAAATTTAACACATTTTGTTTTCCTGGAACTGTTT TTCACAGAGGCCAGGATCCTTCTATATTTCAACATTTAACACATTTTGTTTTCCTGGAACTGTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93302544..93302735 26863196 MeRIP-seq:(Medium) rs1276671561 Functional Loss SNV dbSNP153 33..33 33 - - - 105398 RMVar_ID_105398 Human_SNP_ID_407235643 m1A Human chr9 + 93451858 93451858 93451858 CGCCCGCCAGCCCGCCCGCGCGCCACGGCCCCACCACCCCCGGCCCCGCCGCCCCCCGCCCGCAC CGCCCGCCAGCCCGCCCGCGCGCCACGGCCCCCCCACCCCCGGCCCCGCCGCCCCCCGCCCGCAC A C FAM120A Ensembl:ENSG00000048828 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr9:93451771..93451970 26863410 MeRIP-seq:(Medium) rs964454546 Functional Loss SNV dbSNP153 33..33 33 - - - 105399 RMVar_ID_105399 Human_SNP_ID_407235668 m1A Human chr9 + 93451889 93451889 93451889 CACCACCCCCGGCCCCGCCGCCCCCCGCCCGCACCCGCGCCCGCGCCCCCGCCGCCGCCATGGGC CACCACCCCCGGCCCCGCCGCCCCCCGCCCGCGCCCGCGCCCGCGCCCCCGCCGCCGCCATGGGC A G FAM120A Ensembl:ENSG00000048828 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93451166..93452350 26863196 MeRIP-seq:(Medium) rs1400688019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5034604 RMVar_hsa_circ_82156 105400 RMVar_ID_105400 Human_SNP_ID_407248369 m1A Human chr9 + 93507392 93507392 93507392 GATGCCATTAATGAGATAAAGATGGTTGGAGGAAGAGCAGATTTGGAGGATGGTTTTGGATACGA GATGCCATTAATGAGATAAAGATGGTTGGAGGGAGAGCAGATTTGGAGGATGGTTTTGGATACGA A G FAM120A Ensembl:ENSG00000048828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93507367..93507702 26863196 MeRIP-seq:(Medium) rs753456260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16741856,Human_RBP_ID_23094085,Human_RBP_ID_24314038 RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_302669,RMVar_hsa_circ_341422,RMVar_hsa_circ_357743,RMVar_hsa_circ_293842,RMVar_hsa_circ_273726,RMVar_hsa_circ_119641,RMVar_hsa_circ_257868,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257870,RMVar_hsa_circ_257869,RMVar_hsa_circ_257866,RMVar_hsa_circ_257867,RMVar_hsa_circ_257865,RMVar_hsa_circ_57281,RMVar_hsa_circ_257863,RMVar_hsa_circ_372636,RMVar_hsa_circ_95302,RMVar_hsa_circ_280648,RMVar_hsa_circ_77870,RMVar_hsa_circ_257879,RMVar_hsa_circ_257880,RMVar_hsa_circ_257877,RMVar_hsa_circ_257878,RMVar_hsa_circ_318384,RMVar_hsa_circ_374941,RMVar_hsa_circ_116385,RMVar_hsa_circ_257886,RMVar_hsa_circ_257887 105401 RMVar_ID_105401 Human_SNP_ID_407253598 m1A Human chr9 - 93529484 93529484 93529484 CTCAGCACCTCAGGTGCGACGGGGGGCAGGGGAGGTGTGGTGATGTCCATGTGGTTCCTGGTGGG CTCAGCACCTCAGGTGCGACGGGGGGCAGGGGGGGTGTGGTGATGTCCATGTGGTTCCTGGTGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93529312..93529524 26863196 MeRIP-seq:(Medium) rs879268372 Functional Loss SNV dbSNP153 33..33 33 - - - 105402 RMVar_ID_105402 Human_SNP_ID_407254721 m1A Human chr9 - 93534760 93534760 93534760 TTCCCACCTAAGTCTACTAATACAAACTCTTTATCAGGACTGTCTAATTTTTTCCTATTCTCTCT TTCCCACCTAAGTCTACTAATACAAACTCTTTTTCAGGACTGTCTAATTTTTTCCTATTCTCTCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:93534756..93534892 26863196 MeRIP-seq:(Medium) rs1030937406 Functional Loss SNV dbSNP153 33..33 33 - - - 105403 RMVar_ID_105403 Human_SNP_ID_407258355 m1A Human chr9 + 93550675 93550675 93550675 GGCGCTGTCCCCCAAACTCTACGAGCCTGATCAGCTCCAGGAGCTCAAGGTAATTTATCAGCCTC GGCGCTGTCCCCCAAACTCTACGAGCCTGATCCGCTCCAGGAGCTCAAGGTAATTTATCAGCCTC A C FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:93550626..93550700 26863196 MeRIP-seq:(Medium) rs1270779395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8930105,Human_RBP_ID_19143537 Human_Splice_Rec_1062658,Human_Splice_Rec_1062659,Human_Splice_Rec_1062712,Human_Splice_Rec_1062713 RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_357743,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257866,RMVar_hsa_circ_257865,RMVar_hsa_circ_257863,RMVar_hsa_circ_95302,RMVar_hsa_circ_257877,RMVar_hsa_circ_374941,RMVar_hsa_circ_116385,RMVar_hsa_circ_29491,RMVar_hsa_circ_76732,RMVar_hsa_circ_317606,RMVar_hsa_circ_257886,RMVar_hsa_circ_257887,RMVar_hsa_circ_266951,RMVar_hsa_circ_257888,RMVar_hsa_circ_100907,RMVar_hsa_circ_257893,RMVar_hsa_circ_257896,RMVar_hsa_circ_309814,RMVar_hsa_circ_19912,RMVar_hsa_circ_112639,RMVar_hsa_circ_257897,RMVar_hsa_circ_257900,RMVar_hsa_circ_329191 105404 RMVar_ID_105404 Human_SNP_ID_407258356 m1A Human chr9 + 93550675 93550675 93550675 GGCGCTGTCCCCCAAACTCTACGAGCCTGATCAGCTCCAGGAGCTCAAGGTAATTTATCAGCCTC GGCGCTGTCCCCCAAACTCTACGAGCCTGATCGGCTCCAGGAGCTCAAGGTAATTTATCAGCCTC A G FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:93550626..93550700 26863196 MeRIP-seq:(Medium) rs1270779395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8930105,Human_RBP_ID_19143537 Human_Splice_Rec_1062658,Human_Splice_Rec_1062659,Human_Splice_Rec_1062712,Human_Splice_Rec_1062713 RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_357743,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257866,RMVar_hsa_circ_257865,RMVar_hsa_circ_257863,RMVar_hsa_circ_95302,RMVar_hsa_circ_257877,RMVar_hsa_circ_374941,RMVar_hsa_circ_116385,RMVar_hsa_circ_29491,RMVar_hsa_circ_76732,RMVar_hsa_circ_317606,RMVar_hsa_circ_257886,RMVar_hsa_circ_257887,RMVar_hsa_circ_266951,RMVar_hsa_circ_257888,RMVar_hsa_circ_100907,RMVar_hsa_circ_257893,RMVar_hsa_circ_257896,RMVar_hsa_circ_309814,RMVar_hsa_circ_19912,RMVar_hsa_circ_112639,RMVar_hsa_circ_257897,RMVar_hsa_circ_257900,RMVar_hsa_circ_329191 105405 RMVar_ID_105405 Human_SNP_ID_407260140 m1A Human chr9 + 93558672 93558672 93558672 TTCCGTGTGGCGGCAGCATCGGGACACTGCGGAGCCTTCTCAGGCAGTGACAGCAGCAGGACTAG TTCCGTGTGGCGGCAGCATCGGGACACTGCGGCGCCTTCTCAGGCAGTGACAGCAGCAGGACTAG A C FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93558623..93558811 26863196 MeRIP-seq:(Medium) rs370422795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90139,Human_RBP_ID_846155,Human_RBP_ID_7948320,Human_RBP_ID_8929707,Human_RBP_ID_9315598,Human_RBP_ID_17716944,Human_RBP_ID_19023976,Human_RBP_ID_27833190 Human_Splice_Rec_1062664,Human_Splice_Rec_1062665,Human_Splice_Rec_1062726,Human_Splice_Rec_1062727 RMVar_hsa_circ_85635,RMVar_hsa_circ_2710,RMVar_hsa_circ_257863,RMVar_hsa_circ_95302,RMVar_hsa_circ_257877,RMVar_hsa_circ_116385,RMVar_hsa_circ_76732,RMVar_hsa_circ_257887,RMVar_hsa_circ_266951,RMVar_hsa_circ_257888 105406 RMVar_ID_105406 Human_SNP_ID_407260141 m1A Human chr9 + 93558672 93558672 93558672 TTCCGTGTGGCGGCAGCATCGGGACACTGCGGAGCCTTCTCAGGCAGTGACAGCAGCAGGACTAG TTCCGTGTGGCGGCAGCATCGGGACACTGCGGGGCCTTCTCAGGCAGTGACAGCAGCAGGACTAG A G FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93558623..93558811 26863196 MeRIP-seq:(Medium) rs370422795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90139,Human_RBP_ID_846155,Human_RBP_ID_7948320,Human_RBP_ID_8929707,Human_RBP_ID_9315598,Human_RBP_ID_17716944,Human_RBP_ID_19023976,Human_RBP_ID_27833190 Human_Splice_Rec_1062664,Human_Splice_Rec_1062665,Human_Splice_Rec_1062726,Human_Splice_Rec_1062727 RMVar_hsa_circ_85635,RMVar_hsa_circ_2710,RMVar_hsa_circ_257863,RMVar_hsa_circ_95302,RMVar_hsa_circ_257877,RMVar_hsa_circ_116385,RMVar_hsa_circ_76732,RMVar_hsa_circ_257887,RMVar_hsa_circ_266951,RMVar_hsa_circ_257888 105407 RMVar_ID_105407 Human_SNP_ID_407260146 m1A Human chr9 - 93558679 93558679 93558679 GGACTTGCTAGTCCTGCTGCTGTCACTGCCTGAGAAGGCTCCGCAGTGTCCCGATGCTGCCGCCA GGACTTGCTAGTCCTGCTGCTGTCACTGCCTGGGAAGGCTCCGCAGTGTCCCGATGCTGCCGCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:93557980..93558700 32194978 MeRIP-seq:(Medium) rs1197181268 Functional Loss SNV dbSNP153 33..33 33 - - - 105408 RMVar_ID_105408 Human_SNP_ID_407266991 m1A Human chr9 - 93586862 93586862 93586862 CACAGACTCGCAGGCGGCTGGTGATGAGGGCCATGCCACCCCAACCCTGTCCCCCAGCACTAGCT CACAGACTCGCAGGCGGCTGGTGATGAGGGCCGTGCCACCCCAACCCTGTCCCCCAGCACTAGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93586855..93586950 26863196 MeRIP-seq:(Medium) rs1385447644 Functional Loss SNV dbSNP153 33..33 33 - - - 105409 RMVar_ID_105409 Human_SNP_ID_407267193 m1A Human chr9 + 93587521 93587521 93587521 ATGGAGGAGCCCCGGGTGAGGGATGATGGAGGAGTCCCAGATAGTGGATGGAGGAGCCCCGGGTG ATGGAGGAGCCCCGGGTGAGGGATGATGGAGGCGTCCCAGATAGTGGATGGAGGAGCCCCGGGTG A C PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:93587084..93587627;chr9:93587042..93587620;chr9:93587116..93587609 26863196 MeRIP-seq:(Medium) rs148880827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9442285 105410 RMVar_ID_105410 Human_SNP_ID_407270369 m1A Human chr9 + 93600105 93600104 93600105 ATGTGTATGATGTTTGTGTCTGTGTGGTCTGTATGTGTGTAGTATGTGTGTGGTATGTGTGTAAT ATGTGTATGATGTTTGTGTCTGTGTGGTCTGT_TGTGTGTAGTATGTGTGTGGTATGTGTGTAAT TA T PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93600054..93600179 26863196 MeRIP-seq:(Medium) rs1419406254 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5309188,Human_RBP_ID_24314208 105411 RMVar_ID_105411 Human_SNP_ID_407271361 m1A Human chr9 + 93604152 93604152 93604152 CTGAGATGGGGACACCCCTCTGAGATGGGAAAAACAGGTTGATGTGTGGTAGGGAAGAGGCCTGC CTGAGATGGGGACACCCCTCTGAGATGGGAAAGACAGGTTGATGTGTGGTAGGGAAGAGGCCTGC A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93604144..93604284 26863196 MeRIP-seq:(Medium) rs1464958754 Functional Loss SNV dbSNP153 33..33 33 - - - 105412 RMVar_ID_105412 Human_SNP_ID_407274093 m1A Human chr9 + 93615103 93615086 93615104 TGGTGGTGATGGTAGTGATGGTGATGGTAATAAAGATGGTGATGGTGATGGCGATGATGATGGTG TGGTGGTGATGGTAGT__________________GATGGTGATGGTGATGGCGATGATGATGGTG TGATGGTGATGGTAATAAA T PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:93614769..93615395 26863196 MeRIP-seq:(Medium) rs1225677727 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_24314242 105413 RMVar_ID_105413 Human_SNP_ID_407274110 m1A Human chr9 + 93615127 93615127 93615127 TGGTAATAAAGATGGTGATGGTGATGGCGATGATGATGGTGATGGTGATAGTAATGGTGATGATG TGGTAATAAAGATGGTGATGGTGATGGCGATGGTGATGGTGATGGTGATAGTAATGGTGATGATG A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93614763..93615432 26863196 MeRIP-seq:(Medium) rs1222290282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24314242 105414 RMVar_ID_105414 Human_SNP_ID_407276610 m1A Human chr9 - 93624413 93624413 93624413 ACCACCACCACCATTACCAACATTGCCACACCATCATTATCATCATCACCTCCACCCTCATCACC ACCACCACCACCATTACCAACATTGCCACACCTTCATTATCATCATCACCTCCACCCTCATCACC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93624250..93624890 26863196 MeRIP-seq:(Medium) rs973937323 Functional Loss SNV dbSNP153 33..33 33 - - - 105415 RMVar_ID_105415 Human_SNP_ID_407276772 m1A Human chr9 - 93624827 93624827 93624827 CCACTATCATCACCACCACCATCATCATCATCACCATCATCATCACCATCACCATCACCAGCACT CCACTATCATCACCACCACCATCATCATCATCGCCATCATCATCACCATCACCATCACCAGCACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93624701..93624878 26863196 MeRIP-seq:(Medium) rs1486858526 Functional Loss SNV dbSNP153 33..33 33 - - - 105416 RMVar_ID_105416 Human_SNP_ID_407285704 m1A Human chr9 - 93660398 93660398 93660398 AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTAGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTTGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:93660315..93660405 26863410 MeRIP-seq:(Medium) rs1359693869 Functional Loss SNV dbSNP153 33..33 33 - - - 105417 RMVar_ID_105417 Human_SNP_ID_407285705 m1A Human chr9 - 93660398 93660398 93660398 AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTAGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTGGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:93660315..93660405 26863410 MeRIP-seq:(Medium) rs1359693869 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 105418 RMVar_ID_105418 Human_SNP_ID_407285706 m1A Human chr9 - 93660398 93660398 93660398 AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTAGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG AGCTTCAGCGTTTTGGGGGGCCTTGGGGGCTTCGGGGGCTTCGGGGGCTTGGGGATTTTGGATGG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:93660315..93660405 26863410 MeRIP-seq:(Medium) rs1359693869 Functional Loss SNV dbSNP153 33..33 33 - - - 105419 RMVar_ID_105419 Human_SNP_ID_407285999 m1A Human chr9 - 93661500 93661500 93661500 ATCTATTCATCCATTCGTTAATCCATTCAACCATCCATCTATCCAGCCATTCACTGATTCATTCA ATCTATTCATCCATTCGTTAATCCATTCAACCGTCCATCTATCCAGCCATTCACTGATTCATTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93661487..93662444 26863196 MeRIP-seq:(Medium) rs543485542 Functional Loss SNV dbSNP153 33..33 33 - - - 105420 RMVar_ID_105420 Human_SNP_ID_407286052 m1A Human chr9 + 93661634 93661634 93661634 GGTGAATGGGTGGATGGATGGATGGAAGGACGAATAAATGAATGGGTGGGTAGATGAATGGAATA GGTGAATGGGTGGATGGATGGATGGAAGGACGGATAAATGAATGGGTGGGTAGATGAATGGAATA A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93661628..93662436 26863196 MeRIP-seq:(Medium) rs981793237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5658547 RMVar_hsa_circ_2463,RMVar_hsa_circ_106782,RMVar_hsa_circ_257902,RMVar_hsa_circ_19147 105421 RMVar_ID_105421 Human_SNP_ID_407286330 m1A Human chr9 + 93662548 93662542 93662549 ATGGATGGATGGGTGGGCGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGAACAAA ATGGATGGATGGGTGGGCGGATGGATG_______GGATGGATGGATGGATGGATGGATGAACAAA GGATGGAT G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93662537..93662722 26863196 MeRIP-seq:(Medium) rs1401030388 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_2463,RMVar_hsa_circ_106782,RMVar_hsa_circ_257902,RMVar_hsa_circ_19147 105422 RMVar_ID_105422 Human_SNP_ID_407286333 m1A Human chr9 + 93662548 93662547 93662549 ATGGATGGATGGGTGGGCGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGAACAAA ATGGATGGATGGGTGGGCGGATGGATGGATGG__GGATGGATGGATGGATGGATGGATGAACAAA GAT G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:93662537..93662722 26863196 MeRIP-seq:(Medium) rs1467815530 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_2463,RMVar_hsa_circ_106782,RMVar_hsa_circ_257902,RMVar_hsa_circ_19147 105423 RMVar_ID_105423 Human_SNP_ID_407286366 m1A Human chr9 + 93662578 93662577 93662579 GGATGGATGGATGGATGGATGGATGGATGAACAAATGCATGGTGCATGGATGGATGAATGAACGA GGATGGATGGATGGATGGATGGATGGATGAAC__ATGCATGGTGCATGGATGGATGAATGAACGA CAA C PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93662566..93662706 26863196 MeRIP-seq:(Medium) rs1183003695 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_2463,RMVar_hsa_circ_106782,RMVar_hsa_circ_257902,RMVar_hsa_circ_19147 105424 RMVar_ID_105424 Human_SNP_ID_407288842 m1A Human chr9 + 93671448 93671448 93671448 GTAGGTACAGGTGTAGATGCAGGTGGGTGTGGATGTAGGTACAGGTGTAGATGCAGATGTGGGTG GTAGGTACAGGTGTAGATGCAGGTGGGTGTGGGTGTAGGTACAGGTGTAGATGCAGATGTGGGTG A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:93671397..93671516;chr9:93671381..93671514 26863196 MeRIP-seq:(Medium) rs1218823236 Functional Loss SNV dbSNP153 33..33 33 - - - 105425 RMVar_ID_105425 Human_SNP_ID_407288848 m1A Human chr9 + 93671472 93671472 93671472 GGGTGTGGATGTAGGTACAGGTGTAGATGCAGATGTGGGTGTGGGAGTAGGTACAGGTGTAGATG GGGTGTGGATGTAGGTACAGGTGTAGATGCAGCTGTGGGTGTGGGAGTAGGTACAGGTGTAGATG A C PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93671385..93671526 26863196 MeRIP-seq:(Medium) rs28530486 Functional Loss SNV dbSNP153 33..33 33 - - - 105426 RMVar_ID_105426 Human_SNP_ID_407288849 m1A Human chr9 + 93671472 93671472 93671472 GGGTGTGGATGTAGGTACAGGTGTAGATGCAGATGTGGGTGTGGGAGTAGGTACAGGTGTAGATG GGGTGTGGATGTAGGTACAGGTGTAGATGCAGGTGTGGGTGTGGGAGTAGGTACAGGTGTAGATG A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93671385..93671526 26863196 MeRIP-seq:(Medium) rs28530486 Functional Loss SNV dbSNP153 33..33 33 - - - 105427 RMVar_ID_105427 Human_SNP_ID_407288850 m1A Human chr9 + 93671472 93671472 93671472 GGGTGTGGATGTAGGTACAGGTGTAGATGCAGATGTGGGTGTGGGAGTAGGTACAGGTGTAGATG GGGTGTGGATGTAGGTACAGGTGTAGATGCAGTTGTGGGTGTGGGAGTAGGTACAGGTGTAGATG A T PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93671385..93671526 26863196 MeRIP-seq:(Medium) rs28530486 Functional Loss SNV dbSNP153 33..33 33 - - - 105428 RMVar_ID_105428 Human_SNP_ID_407289215 m1A Human chr9 - 93672471 93672435 93672471 CTGCATGTACACCTGTGCCTACTCCCACACTCACACCTGTGCCTACTCCCACACCCACACCTGCA CTGCATGTACACCTGTGCCTACTCCCACACTC_________________________________ CAGGTGCAGGTGTGGGTGTGGGAGTAGGCACAGGTGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93672463..93672558 26863196 MeRIP-seq:(Medium) rs1564403804 Functional Loss DEL dbSNP153 33..65 33 - - - 105429 RMVar_ID_105429 Human_SNP_ID_407289271 m1A Human chr9 + 93672598 93672598 93672598 ATGGGTGTAGGTGTAGGCACCAGTGTAGATGGAGGTGTGGGTATGGGTGTAGGCACAGGTGTAGA ATGGGTGTAGGTGTAGGCACCAGTGTAGATGGGGGTGTGGGTATGGGTGTAGGCACAGGTGTAGA A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:93672367..93672647 26863196 MeRIP-seq:(Medium) rs1197045465 Functional Loss SNV dbSNP153 33..33 33 - - - 105430 RMVar_ID_105430 Human_SNP_ID_407289356 m1A Human chr9 + 93672850 93672849 93672850 GTAGGTGTAGGAACAGGTGTAGATGCAGGTGCAGGGGTGGAGGTAGGTACAGGTGTAGATGCAGG GTAGGTGTAGGAACAGGTGTAGATGCAGGTGC_GGGGTGGAGGTAGGTACAGGTGTAGATGCAGG CA C PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93672804..93672953 26863196 MeRIP-seq:(Medium) rs1353410308 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5226685 105431 RMVar_ID_105431 Human_SNP_ID_407289357 m1A Human chr9 + 93672850 93672850 93672850 GTAGGTGTAGGAACAGGTGTAGATGCAGGTGCAGGGGTGGAGGTAGGTACAGGTGTAGATGCAGG GTAGGTGTAGGAACAGGTGTAGATGCAGGTGCGGGGGTGGAGGTAGGTACAGGTGTAGATGCAGG A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93672804..93672953 26863196 MeRIP-seq:(Medium) rs1383843182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226685 105432 RMVar_ID_105432 Human_SNP_ID_407289384 m1A Human chr9 - 93672919 93672919 93672919 ATACGTGCATCTACACCTGTACCTACCCTCACACCTGCACCTGCATCTACACCTGTACCTCCAAC ATACGTGCATCTACACCTGTACCTACCCTCACCCCTGCACCTGCATCTACACCTGTACCTCCAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:93672330..93673221 26863196 MeRIP-seq:(Medium) rs1439713577 Functional Loss SNV dbSNP153 33..33 33 - - - 105433 RMVar_ID_105433 Human_SNP_ID_407360795 m1A Human chr9 + 93955351 93955351 93955351 GGGCGCGCGGGGCTCGGCCGGTCGAACCCGGGACTGCGCCCCCTCCCCACGCCGCCGCGCCTCTT GGGCGCGCGGGGCTCGGCCGGTCGAACCCGGGTCTGCGCCCCCTCCCCACGCCGCCGCGCCTCTT A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:93955273..93955400 26863410 MeRIP-seq:(Medium) rs1376358253 Functional Loss SNV dbSNP153 33..33 33 - - - 105434 RMVar_ID_105434 Human_SNP_ID_407378413 m1A Human chr9 - 94030901 94030901 94030901 CTCCCGACGCGCCCTGGAGGCAGAGGGGTCCCAGCCCAGCCCGCCGGACAACGTCCTGGGGCGAG CTCCCGACGCGCCCTGGAGGCAGAGGGGTCCCGGCCCAGCCCGCCGGACAACGTCCTGGGGCGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:94030850..94031073 26863196 MeRIP-seq:(Medium) rs915102575 Functional Loss SNV dbSNP153 33..33 33 - - - 105435 RMVar_ID_105435 Human_SNP_ID_407379987 m1A Human chr9 + 94038027 94038027 94038027 ACCTTCGTTGCGCCAGCGACAAAAAAGAATTAAATATGGGTGATGTTGAGAAGGGCAAGAAGATT ACCTTCGTTGCGCCAGCGACAAAAAAGAATTATATATGGGTGATGTTGAGAAGGGCAAGAAGATT A T PTPDC1 Ensembl:ENSG00000158079 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:94037957..94038131 26863196 MeRIP-seq:(Medium) rs1387005665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3227013 105436 RMVar_ID_105436 Human_SNP_ID_407432609 m1A Human chr9 - 94260625 94260625 94260625 CCGAGGGAGCCACACAGCTGCAGAAGCCGACAATCTGGATACAAGCACGCCCCCATGCAACCCAC CCGAGGGAGCCACACAGCTGCAGAAGCCGACAGTCTGGATACAAGCACGCCCCCATGCAACCCAC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:94260484..94260662 26863196 MeRIP-seq:(Medium) rs1341106009 Functional Loss SNV dbSNP153 33..33 33 - - - 105437 RMVar_ID_105437 Human_SNP_ID_407455115 m1A Human chr9 + 94347462 94347462 94347462 TCCCCATTTTCCTCATTAGCATTCCCGTTAGCAGGGGCGTCTCTTCCATTTTCCGCGTCTTTCAC TCCCCATTTTCCTCATTAGCATTCCCGTTAGCCGGGGCGTCTCTTCCATTTTCCGCGTCTTTCAC A C AL691447.2 Ensembl:ENSG00000232063 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:94347439..94347507 26863196 MeRIP-seq:(Medium) rs545001578 Functional Loss SNV dbSNP153 33..33 33 - - - 105438 RMVar_ID_105438 Human_SNP_ID_407460743 m1A Human chr9 + 94374602 94374602 94374602 GTAACTGCGAGAGTCGGGGTCGGTGCGGTTTGATAAGTGGTCGGTTCCTGGAGCTGCGGTCTTCT GTAACTGCGAGAGTCGGGGTCGGTGCGGTTTGCTAAGTGGTCGGTTCCTGGAGCTGCGGTCTTCT A C MFSD14B Ensembl:ENSG00000148110 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:94374591..94374709 26863196 MeRIP-seq:(Medium) rs3118796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1707741,Human_RBP_ID_5036252,Human_RBP_ID_5482347,Human_RBP_ID_7948916,Human_RBP_ID_18139901 105439 RMVar_ID_105439 Human_SNP_ID_407460744 m1A Human chr9 + 94374602 94374602 94374602 GTAACTGCGAGAGTCGGGGTCGGTGCGGTTTGATAAGTGGTCGGTTCCTGGAGCTGCGGTCTTCT GTAACTGCGAGAGTCGGGGTCGGTGCGGTTTGGTAAGTGGTCGGTTCCTGGAGCTGCGGTCTTCT A G MFSD14B Ensembl:ENSG00000148110 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:94374591..94374709 26863196 MeRIP-seq:(Medium) rs3118796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1707741,Human_RBP_ID_5036252,Human_RBP_ID_5482347,Human_RBP_ID_7948916,Human_RBP_ID_18139901 105440 RMVar_ID_105440 Human_SNP_ID_407460781 m1A Human chr9 - 94374692 94374680 94374692 CCGCGGCGGCCTGCGGGTCAGGCGGCGGCGCCAGCGGCGGCGCCGAGGGCTGAGGAGGCGGCGGA CCGCGGCGGCCTGCGGGTCAGGCGGCGGCGCC____________GAGGGCTGAGGAGGCGGCGGA CGGCGCCGCCGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:94374599..94374714 26863196 MeRIP-seq:(Medium) rs1241541590 Functional Loss DEL dbSNP153 33..44 33 - - - 105441 RMVar_ID_105441 Human_SNP_ID_407460790 m1A Human chr9 + 94374713 94374695 94374714 GGCGCCGCCGCTGGCGCCGCCGCCTGACCCGCAGGCCGCCGCGGGCCGCAGAGCCCATGAGGGCG GGCGCCGCCGCTGGC___________________GCCGCCGCGGGCCGCAGAGCCCATGAGGGCG CGCCGCCGCCTGACCCGCAG C MFSD14B Ensembl:ENSG00000148110 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:94374615..94415228 26863410 MeRIP-seq:(Medium) rs1303847275 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_256702,Human_RBP_ID_5035756 105442 RMVar_ID_105442 Human_SNP_ID_407504803 m1A Human chr9 + 94541090 94541090 94541090 TCTCTACTCTTTTCTCTTGGCTTGCCTCCTTCACTATGGGCAACCTTCCACCTCCCATTCCTCCT TCTCTACTCTTTTCTCTTGGCTTGCCTCCTTCTCTATGGGCAACCTTCCACCTCCCATTCCTCCT A T RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:94540915..94541120 26863196 MeRIP-seq:(Medium) rs112056268 Functional Loss SNV dbSNP153 33..33 33 - - - 105443 RMVar_ID_105443 Human_SNP_ID_407600140 m1A Human chr9 - 94930701 94930701 94930701 ACTTCTCTCTCTTTCGCCCCTCTTCATCCCCCAGGCAGCTTCCAACATCAGCCACTCCCACCTGC ACTTCTCTCTCTTTCGCCCCTCTTCATCCCCCGGGCAGCTTCCAACATCAGCCACTCCCACCTGC T C AL353768.1 Ensembl:ENSG00000224764 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:94930571..94930871;chr9:94930653..94930878 26863196 MeRIP-seq:(Medium) rs1159946983 Functional Loss SNV dbSNP153 33..33 33 - - - 105444 RMVar_ID_105444 Human_SNP_ID_407602004 m1A Human chr9 + 94938543 94938543 94938543 CACTGAGATGGGTGAAGAGGCAGAGGGAGAGGAATTCAAGGAGCAAAGCCTGGTAGGCATAAAAA CACTGAGATGGGTGAAGAGGCAGAGGGAGAGGGATTCAAGGAGCAAAGCCTGGTAGGCATAAAAA A G AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:94938499..94938619 26863196 MeRIP-seq:(Medium) rs1449831673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_7660,RMVar_hsa_circ_257948,RMVar_hsa_circ_273798,RMVar_hsa_circ_297870,RMVar_hsa_circ_301843,RMVar_hsa_circ_361926,RMVar_hsa_circ_29688,RMVar_hsa_circ_50952,RMVar_hsa_circ_257950,RMVar_hsa_circ_257949,RMVar_hsa_circ_11213 105445 RMVar_ID_105445 Human_SNP_ID_407616617 m1A Human chr9 - 95004263 95004263 95004263 TACACTTACTTTATAAAAATGTGCGATACCCCAAGATTTTCCTCCACCCGCCAAAGGCCTTCTCA TACACTTACTTTATAAAAATGTGCGATACCCCGAGATTTTCCTCCACCCGCCAAAGGCCTTCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95004188..95004329 26863196 MeRIP-seq:(Medium) rs1208025064 Functional Loss SNV dbSNP153 33..33 33 - - - 105446 RMVar_ID_105446 Human_SNP_ID_407616621 m1A Human chr9 - 95004268 95004268 95004268 AAGTTTACACTTACTTTATAAAAATGTGCGATACCCCAAGATTTTCCTCCACCCGCCAAAGGCCT AAGTTTACACTTACTTTATAAAAATGTGCGATTCCCCAAGATTTTCCTCCACCCGCCAAAGGCCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95004217..95004346 26863196 MeRIP-seq:(Medium) rs3208472 Functional Loss SNV dbSNP153 33..33 33 - - - 105447 RMVar_ID_105447 Human_SNP_ID_407616622 m1A Human chr9 - 95004268 95004268 95004268 AAGTTTACACTTACTTTATAAAAATGTGCGATACCCCAAGATTTTCCTCCACCCGCCAAAGGCCT AAGTTTACACTTACTTTATAAAAATGTGCGATGCCCCAAGATTTTCCTCCACCCGCCAAAGGCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95004217..95004346 26863196 MeRIP-seq:(Medium) rs3208472 Functional Loss SNV dbSNP153 33..33 33 - - - 105448 RMVar_ID_105448 Human_SNP_ID_407617009 m1A Human chr9 + 95005219 95005219 95005219 GGAGTGCGGGCTTGCGCGGCAAGTGCGCGCCGAGGTGAGTGCGGGCGGCGCGGTCCCTGCGCCCC GGAGTGCGGGCTTGCGCGGCAAGTGCGCGCCGCGGTGAGTGCGGGCGGCGCGGTCCCTGCGCCCC A C AOPEP Ensembl:ENSG00000148120 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:95005151..95005256;chr9:95004976..95005422 26863196 MeRIP-seq:(Medium) rs192735443 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_962108,Human_RBP_ID_5408425,Human_RBP_ID_19023980,Human_RBP_ID_19143551,Human_RBP_ID_26796407 Human_Splice_Rec_1063182,Human_Splice_Rec_1063183,Human_Splice_Rec_1063212,Human_Splice_Rec_1063213,Human_Splice_Rec_1063242,Human_Splice_Rec_1063243,Human_Splice_Rec_1063268,Human_Splice_Rec_1063269,Human_Splice_Rec_1063302,Human_Splice_Rec_1063303,Human_Splice_Rec_1063322,Human_Splice_Rec_1063323,Human_Splice_Rec_1063334,Human_Splice_Rec_1063335,Human_Splice_Rec_1063342,Human_Splice_Rec_1063343,Human_Splice_Rec_1063348,Human_Splice_Rec_1063349,Human_Splice_Rec_1063354,Human_Splice_Rec_1063355,Human_Splice_Rec_1063364,Human_Splice_Rec_1063365,Human_Splice_Rec_1063374,Human_Splice_Rec_1063375,Human_Splice_Rec_1063388,Human_Splice_Rec_1063389,Human_Splice_Rec_1063395 RMVar_hsa_circ_13382,RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_361926,RMVar_hsa_circ_29688,RMVar_hsa_circ_272980,RMVar_hsa_circ_67341,RMVar_hsa_circ_257957,RMVar_hsa_circ_23042,RMVar_hsa_circ_359538,RMVar_hsa_circ_47402,RMVar_hsa_circ_364246,RMVar_hsa_circ_73834 105449 RMVar_ID_105449 Human_SNP_ID_407626966 m1A Human chr9 + 95044624 95044624 95044624 TGACCCCTTGAATAGTGATTTGAGTAGAGGGCATTCCAGGCAGAGGGCTGAGAAGGCTGCAGAAA TGACCCCTTGAATAGTGATTTGAGTAGAGGGCGTTCCAGGCAGAGGGCTGAGAAGGCTGCAGAAA A G AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95044619..95044720 26863196 MeRIP-seq:(Medium) rs1404177644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23300574 RMVar_hsa_circ_13382,RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_29688,RMVar_hsa_circ_21069,RMVar_hsa_circ_67341,RMVar_hsa_circ_364246,RMVar_hsa_circ_257958 105450 RMVar_ID_105450 Human_SNP_ID_407630792 m1A Human chr9 + 95060751 95060751 95060751 TTCTGGAGCATCTCTTGGAGCAGAAGACTCTGAGCCCCCGAACTCTGCAAAGCCTCCAGAGGACA TTCTGGAGCATCTCTTGGAGCAGAAGACTCTGCGCCCCCGAACTCTGCAAAGCCTCCAGAGGACA A C AOPEP Ensembl:ENSG00000148120 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95060636..95060750 26863196 MeRIP-seq:(Medium) rs118115230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963379,Human_RBP_ID_9407072,Human_RBP_ID_19025153,Human_RBP_ID_19143554,Human_RBP_ID_23094601,Human_RBP_ID_26239470 Human_Splice_Rec_1063186,Human_Splice_Rec_1063187,Human_Splice_Rec_1063216,Human_Splice_Rec_1063217,Human_Splice_Rec_1063246,Human_Splice_Rec_1063247,Human_Splice_Rec_1063272,Human_Splice_Rec_1063273,Human_Splice_Rec_1063306,Human_Splice_Rec_1063307,Human_Splice_Rec_1063346,Human_Splice_Rec_1063352,Human_Splice_Rec_1063358,Human_Splice_Rec_1063359,Human_Splice_Rec_1063368,Human_Splice_Rec_1063369,Human_Splice_Rec_1063378,Human_Splice_Rec_1063379,Human_Splice_Rec_1063398,Human_Splice_Rec_1063399,Human_Splice_Rec_1063408,Human_Splice_Rec_1063409,Human_Splice_Rec_1063414,Human_Splice_Rec_1063415 Human_miRNA_ID_2269337,Human_miRNA_ID_2269338 RMVar_hsa_circ_13382,RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_29688,RMVar_hsa_circ_21069,RMVar_hsa_circ_67341,RMVar_hsa_circ_364246,RMVar_hsa_circ_257959,RMVar_hsa_circ_299975,RMVar_hsa_circ_257958,RMVar_hsa_circ_312580,RMVar_hsa_circ_357801,RMVar_hsa_circ_257960 105451 RMVar_ID_105451 Human_SNP_ID_407636370 m1A Human chr9 + 95083357 95083357 95083357 ACAGAGCACGCACAGCACACACCACACAGCGCACGCACCACACAGAGCACACGCGGCACACACAG ACAGAGCACGCACAGCACACACCACACAGCGCGCGCACCACACAGAGCACACGCGGCACACACAG A G AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95083244..95083453 26863196 MeRIP-seq:(Medium) rs1281449738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184843,Human_RBP_ID_219714,Human_RBP_ID_3228800 105452 RMVar_ID_105452 Human_SNP_ID_407664271 m1A Human chr9 + 95190554 95190554 95190554 CCCTACCAGTTCACCAGTCAGAACTCCATGCTACAAACCGTGGGATCCACCCCTGCACCCTCTTG CCCTACCAGTTCACCAGTCAGAACTCCATGCTGCAAACCGTGGGATCCACCCCTGCACCCTCTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95190503..95190589 26863196 MeRIP-seq:(Medium) rs1016460555 Functional Loss SNV dbSNP153 33..33 33 - - - 105453 RMVar_ID_105453 Human_SNP_ID_407694838 m1A Human chr9 - 95317343 95317338 95317344 GAGGGGTTCCCGCCGGCGCAGGGCTGTGGCTAAGGCTGAGGCGGGAGGCGGGAGGCGGGAGGCGG GAGGGGTTCCCGCCGGCGCAGGGCTGTGGCT______GAGGCGGGAGGCGGGAGGCGGGAGGCGG CAGCCTT C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95317335..95317495 26863196 MeRIP-seq:(Medium) rs1422650679 Functional Loss DEL dbSNP153 32..37 33 - - - 105454 RMVar_ID_105454 Human_SNP_ID_407694843 m1A Human chr9 - 95317343 95317343 95317343 GAGGGGTTCCCGCCGGCGCAGGGCTGTGGCTAAGGCTGAGGCGGGAGGCGGGAGGCGGGAGGCGG GAGGGGTTCCCGCCGGCGCAGGGCTGTGGCTATGGCTGAGGCGGGAGGCGGGAGGCGGGAGGCGG T A FANCC Ensembl:ENSG00000158169 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95317335..95317495 26863196 MeRIP-seq:(Medium) rs1168434050 Functional Loss SNV dbSNP153 33..33 33 - - - 105455 RMVar_ID_105455 Human_SNP_ID_407694964 m1A Human chr9 - 95317623 95317623 95317623 GGGAAAATTCCAAAAAAACTCAAAAAGCCAATACGAGGCAAAGCCAAATTTTCAAGCCACAGATC GGGAAAATTCCAAAAAAACTCAAAAAGCCAATTCGAGGCAAAGCCAAATTTTCAAGCCACAGATC T A FANCC Ensembl:ENSG00000158169 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95317573..95317701 26863196 MeRIP-seq:(Medium) rs1490861386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1063431,Human_Splice_Rec_1063551,Human_Splice_Rec_1063607,Human_Splice_Rec_1063619,Human_Splice_Rec_1063685 105456 RMVar_ID_105456 Human_SNP_ID_407694968 m1A Human chr9 - 95317634 95317634 95317634 CGGGCGACCGCGGGAAAATTCCAAAAAAACTCAAAAAGCCAATACGAGGCAAAGCCAAATTTTCA CGGGCGACCGCGGGAAAATTCCAAAAAAACTCGAAAAGCCAATACGAGGCAAAGCCAAATTTTCA T C FANCC Ensembl:ENSG00000158169 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95317583..95317666 26863196 MeRIP-seq:(Medium) rs1400683115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036253,Human_RBP_ID_5431426,Human_RBP_ID_8159168,Human_RBP_ID_9239512,Human_RBP_ID_18140055 105457 RMVar_ID_105457 Human_SNP_ID_407694970 m1A Human chr9 - 95317638 95317638 95317638 CTGCCGGGCGACCGCGGGAAAATTCCAAAAAAACTCAAAAAGCCAATACGAGGCAAAGCCAAATT CTGCCGGGCGACCGCGGGAAAATTCCAAAAAAGCTCAAAAAGCCAATACGAGGCAAAGCCAAATT T C FANCC Ensembl:ENSG00000158169 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:95317470..95317669 26863196 MeRIP-seq:(Medium) rs1339506933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035033,Human_RBP_ID_5431426,Human_RBP_ID_8159168,Human_RBP_ID_9239512,Human_RBP_ID_18140055 105458 RMVar_ID_105458 Human_SNP_ID_407715803 m1A Human chr9 - 95407743 95407741 95407744 GAAAGAAAGAAAAGGAGAGAGAGAAAGAAAGAAGGAAAGAAAGAAAGGAAGGAAGAAAAAGAGGA GAAAGAAAGAAAAGGAGAGAGAGAAAGAAAG___GAAAGAAAGAAAGGAAGGAAGAAAAAGAGGA CCTT C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95407659..95407822 26863196 MeRIP-seq:(Medium) rs913725492 Functional Loss DEL dbSNP153 32..34 33 - - - 105459 RMVar_ID_105459 Human_SNP_ID_407720194 m1A Human chr9 - 95426779 95426779 95426779 AGGCAGGGCCGGGCCGGGCCGGGTGCGCGGGCACAAAGGGGCCGCTGCACATGGCAGGCAGGCGA AGGCAGGGCCGGGCCGGGCCGGGTGCGCGGGCTCAAAGGGGCCGCTGCACATGGCAGGCAGGCGA T A FANCC Ensembl:ENSG00000158169 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95426685..95426879 26863196 MeRIP-seq:(Medium) rs1354499728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18427319 Human_Splice_Rec_1063595,Human_Splice_Rec_1063691 105460 RMVar_ID_105460 Human_SNP_ID_407741352 m1A Human chr9 - 95504568 95504568 95504568 GGGAGGGCCGCTGCCGTAGATTCTTGGACAGAATAGGGCATGAGCACAGGGAGGGCCGGCTCATC GGGAGGGCCGCTGCCGTAGATTCTTGGACAGAGTAGGGCATGAGCACAGGGAGGGCCGGCTCATC T C PTCH1 Ensembl:ENSG00000185920 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95504566..95504735 26863196 MeRIP-seq:(Medium) rs529615395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16749859 105461 RMVar_ID_105461 Human_SNP_ID_407743264 m1A Human chr9 + 95509054 95509054 95509054 CTGCTGGGTTCGCGGTGGCTGCTCGGTCCCGGACTCTGCTTTCTTGTGCTCCTCGGCAACCCGCT CTGCTGGGTTCGCGGTGGCTGCTCGGTCCCGGGCTCTGCTTTCTTGTGCTCCTCGGCAACCCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95508931..95509217 26863196 MeRIP-seq:(Medium) rs1193626363 Functional Loss SNV dbSNP153 33..33 33 - - - 105462 RMVar_ID_105462 Human_SNP_ID_407743278 m1A Human chr9 + 95509092 95509092 95509092 CTTTCTTGTGCTCCTCGGCAACCCGCTGGACCATTCTGTCCCCGTGCAGCGCGCCTCTCTCGCTC CTTTCTTGTGCTCCTCGGCAACCCGCTGGACCGTTCTGTCCCCGTGCAGCGCGCCTCTCTCGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:95509050..95509145 26863196 MeRIP-seq:(Medium) rs1431617895 Functional Loss SNV dbSNP153 33..33 33 - - - 105463 RMVar_ID_105463 Human_SNP_ID_407828529 m1A Human chr9 - 95858980 95858980 95858980 ATACAGTAGACTATATTATTATATTTTGCAAGAGTATGTATACACGTGTTAGACTTCAAACTCAG ATACAGTAGACTATATTATTATATTTTGCAAGGGTATGTATACACGTGTTAGACTTCAAACTCAG T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95858953..95859023 26863196 MeRIP-seq:(Medium) rs1413892430 Functional Loss SNV dbSNP153 33..33 33 - - - 105464 RMVar_ID_105464 Human_SNP_ID_407863884 m1A Human chr9 + 96006285 96006285 96006285 ACTTCTGGAGGAGGCATAAGAGGCACAGTATCAGGTCCTGAAGTGCAGGAGTAGCGAGAGGATCT ACTTCTGGAGGAGGCATAAGAGGCACAGTATCGGGTCCTGAAGTGCAGGAGTAGCGAGAGGATCT A G ERCC6L2 Ensembl:ENSG00000182150 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:96006235..96006300 26863196 MeRIP-seq:(Medium) rs1287306394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24315659 105465 RMVar_ID_105465 Human_SNP_ID_407942114 m1A Human chr9 - 96322006 96321995 96322007 TACATTTTCTCTTTGTTAAACTTTGTAGGGTTAAATATTTGGTGAGTGGGAATTTTTAATGGACT TACATTTTCTCTTTGTTAAACTTTGTAGGGT____________GAGTGGGAATTTTTAATGGACT CACCAAATATTTA C SLC35D2,AL160269.1 Ensembl:ENSG00000130958,Ensembl:ENSG00000285269 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:96321997..96324106 32194978 MeRIP-seq:(Medium) rs780561335 Functional Loss DEL dbSNP153 32..43 33 - - - Human_Splice_Rec_1064848,Human_Splice_Rec_1064849,Human_Splice_Rec_1064900,Human_Splice_Rec_1064901,Human_Splice_Rec_1064918,Human_Splice_Rec_1064919,Human_Splice_Rec_1064940,Human_Splice_Rec_1064941 RMVar_hsa_circ_57093,RMVar_hsa_circ_272888,RMVar_hsa_circ_343009,RMVar_hsa_circ_365285,RMVar_hsa_circ_370008,RMVar_hsa_circ_350537,RMVar_hsa_circ_326198,RMVar_hsa_circ_258016,RMVar_hsa_circ_258014,RMVar_hsa_circ_258015,RMVar_hsa_circ_91674 105466 RMVar_ID_105466 Human_SNP_ID_407957292 m1A Human chr9 + 96383547 96383547 96383547 GAGGAAGGAGCAGGTCCCGTAGAAGAGCGCCGACAGCAGCCGGGCCACCCGCGAGGGCAGCCGCG GAGGAAGGAGCAGGTCCCGTAGAAGAGCGCCGGCAGCAGCCGGGCCACCCGCGAGGGCAGCCGCG A G RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:96364509..96383612 32194978 MeRIP-seq:(Medium) rs1458927652 Functional Loss SNV dbSNP153 33..33 33 - - - 105467 RMVar_ID_105467 Human_SNP_ID_407957298 m1A Human chr9 + 96383573 96383562 96383574 GCGCCGACAGCAGCCGGGCCACCCGCGAGGGCAGCCGCGCCGCGCCGGGCTCCCCGCCAGCGCCC GCGCCGACAGCAGCCGGGCCAC____________CCGCGCCGCGCCGGGCTCCCCGCCAGCGCCC CCCGCGAGGGCAG C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:96383533..96383667;chr9:96383531..96383662;chr9:96383526..96383638 26863196 MeRIP-seq:(Medium) rs1162082148 Functional Loss DEL dbSNP153 23..34 33 - - - 105468 RMVar_ID_105468 Human_SNP_ID_407965452 m1A Human chr9 - 96417340 96417340 96417340 CGCGGCCCGGGGTCGCTGGGGAGGCCGGGTCAACGGCCACTGACATCCTCCCGGCGGGCTGCCGA CGCGGCCCGGGGTCGCTGGGGAGGCCGGGTCAGCGGCCACTGACATCCTCCCGGCGGGCTGCCGA T C ZNF367,AL133477.1 Ensembl:ENSG00000165244,Ensembl:ENSG00000286835 Protein coding,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:96417335..96417532 26863196 MeRIP-seq:(Medium) rs1176452343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906918,Human_RBP_ID_5329546,Human_RBP_ID_5407280,Human_RBP_ID_9339497,Human_RBP_ID_18467806,Human_RBP_ID_22118749,Human_RBP_ID_22733387,Human_RBP_ID_27843608 105469 RMVar_ID_105469 Human_SNP_ID_407965707 m1A Human chr9 - 96417959 96417959 96417959 GCCGCCGCCGCCGCCCGTCATCTTCTGCCACGACTCCCCGAAGCGGGTGCTGGTGTCGGTCATCA GCCGCCGCCGCCGCCCGTCATCTTCTGCCACGCCTCCCCGAAGCGGGTGCTGGTGTCGGTCATCA T G ZNF367 Ensembl:ENSG00000165244 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:96398281..96418329 32194978 MeRIP-seq:(Medium) rs759464009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035335,Human_RBP_ID_8709179,Human_RBP_ID_16751632,Human_RBP_ID_17672549,Human_RBP_ID_18140273 105470 RMVar_ID_105470 Human_SNP_ID_407974679 m1A Human chr9 - 96450291 96450291 96450291 GCGGCGCCAGCGGCAGCCACGGGACTCCCCAGAGCGCCCTTCATGCCGCCGCGACCACTGCGGGC GCGGCGCCAGCGGCAGCCACGGGACTCCCCAGGGCGCCCTTCATGCCGCCGCGACCACTGCGGGC T C RF00017-4575,RF00017-1003 RNACentral:URS0000918622,RNACentral:URS0000945854 SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:96450194..96450498 26863410 MeRIP-seq:(Medium) rs771995885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16751645 105471 RMVar_ID_105471 Human_SNP_ID_407974753 m1A Human chr9 + 96450496 96450474 96450496 CGGCGGCGGCCGGGGCCGGTCCCCGCGGCGGCAGGAGCCCAGCCGGGGCCTCGGGCCACAGAGCC CGGCGGCGGCC______________________GGAGCCCAGCCGGGGCCTCGGGCCACAGAGCC CGGGGCCGGTCCCCGCGGCGGCA C HABP4 Ensembl:ENSG00000130956 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:96450448..96450575 26863196 MeRIP-seq:(Medium) rs1256303657 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_963393,Human_RBP_ID_3906920,Human_RBP_ID_5035763,Human_RBP_ID_8731101,Human_RBP_ID_26796414 105472 RMVar_ID_105472 Human_SNP_ID_407979003 m1A Human chr9 + 96465717 96465717 96465717 AAGGGACTATTCTTTCTTTCCGTAGAGCAGTCAGAACTGAAGACAACATGGGTGGATGTGGAGTT AAGGGACTATTCTTTCTTTCCGTAGAGCAGTCGGAACTGAAGACAACATGGGTGGATGTGGAGTT A G HABP4 Ensembl:ENSG00000130956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:96465326..96471079 26863196 MeRIP-seq:(Medium) rs1270916996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19023984 Human_Splice_Rec_1064996,Human_Splice_Rec_1064997 RMVar_hsa_circ_287102,RMVar_hsa_circ_301979,RMVar_hsa_circ_32195,RMVar_hsa_circ_284344,RMVar_hsa_circ_258037,RMVar_hsa_circ_258038,RMVar_hsa_circ_258036,RMVar_hsa_circ_16442,RMVar_hsa_circ_258039,RMVar_hsa_circ_258041,RMVar_hsa_circ_306476,RMVar_hsa_circ_309499,RMVar_hsa_circ_300617,RMVar_hsa_circ_258040,RMVar_hsa_circ_90575,RMVar_hsa_circ_258042 105473 RMVar_ID_105473 Human_SNP_ID_407983334 m1A Human chr9 + 96484405 96484401 96484406 TTGAATTAATGGTTATAACTTTTTCTTTATAAAGTAGACATTTTAGTACCATCAAAAAGTATTCT TTGAATTAATGGTTATAACTTTTTCTTTA_____TAGACATTTTAGTACCATCAAAAAGTATTCT ATAAAG A HABP4 Ensembl:ENSG00000130956 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:96484404..96488145 26863196 MeRIP-seq:(Medium) rs1202805223 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_32195,RMVar_hsa_circ_284344,RMVar_hsa_circ_258038,RMVar_hsa_circ_16442,RMVar_hsa_circ_258041,RMVar_hsa_circ_306476,RMVar_hsa_circ_310731 105474 RMVar_ID_105474 Human_SNP_ID_408016495 m1A Human chr9 + 96619399 96619399 96619399 TTTCCGCTTCATGGAGGCGGCCGCGGCCCGTCAGGGGGCCACGACCATGGCCCCGCGCGCCCGCG TTTCCGCTTCATGGAGGCGGCCGCGGCCCGTCCGGGGGCCACGACCATGGCCCCGCGCGCCCGCG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:96619302..96619475 26863410 MeRIP-seq:(Medium) rs1266839705 Functional Loss SNV dbSNP153 33..33 33 - - - 105475 RMVar_ID_105475 Human_SNP_ID_408016646 m1A Human chr9 + 96619788 96619788 96619788 CCGCGGCCGCTGCTGCGTAGGCGCCGGGGCACAGCAGGACGCGGCTCGTGGGGACCCCAGGAGGG CCGCGGCCGCTGCTGCGTAGGCGCCGGGGCACCGCAGGACGCGGCTCGTGGGGACCCCAGGAGGG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:96619689..96619793 26863410 MeRIP-seq:(Medium) rs568260643 Functional Loss SNV dbSNP153 33..33 33 - - - 105476 RMVar_ID_105476 Human_SNP_ID_408065615 m1A Human chr9 - 96820556 96820540 96820557 GACAGAGCAAGACTCTATCTCAAAAAAAAGAAAAAAAAAAAAAAAAGATTCACTATTGAACAACC GACAGAGCAAGACTCTATCTCAAAAAAAAGA_________________TTCACTATTGAACAACC ATCTTTTTTTTTTTTTTT A ZNF782 Ensembl:ENSG00000196597 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:96820542..96820627 26863410 MeRIP-seq:(Medium) rs1313493603 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_26238811 RMVar_hsa_circ_258069,RMVar_hsa_circ_258067,RMVar_hsa_circ_258070,RMVar_hsa_circ_258072,RMVar_hsa_circ_258073,RMVar_hsa_circ_258071 105477 RMVar_ID_105477 Human_SNP_ID_408065632 m1A Human chr9 - 96820556 96820556 96820556 GACAGAGCAAGACTCTATCTCAAAAAAAAGAAAAAAAAAAAAAAAAGATTCACTATTGAACAACC GACAGAGCAAGACTCTATCTCAAAAAAAAGAAGAAAAAAAAAAAAAGATTCACTATTGAACAACC T C ZNF782 Ensembl:ENSG00000196597 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:96820542..96820627 26863410 MeRIP-seq:(Medium) rs10979164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26238811 RMVar_hsa_circ_258069,RMVar_hsa_circ_258067,RMVar_hsa_circ_258070,RMVar_hsa_circ_258072,RMVar_hsa_circ_258073,RMVar_hsa_circ_258071 105478 RMVar_ID_105478 Human_SNP_ID_408072964 m1A Human chr9 + 96854186 96854186 96854186 GTTGTCGCCCGCGTTACAAATGCGCTTTCCCCACCCCCGCCGCCGCTCGCGCCGGGCTCCGGTCC GTTGTCGCCCGCGTTACAAATGCGCTTTCCCCCCCCCCGCCGCCGCTCGCGCCGGGCTCCGGTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:96854142..96854476 26863196 MeRIP-seq:(Medium) rs905099845 Functional Loss SNV dbSNP153 33..33 33 - - - 105479 RMVar_ID_105479 Human_SNP_ID_408072970 m1A Human chr9 - 96854200 96854200 96854200 GGCCGCGGTGTGCGGGACCGGAGCCCGGCGCGAGCGGCGGCGGGGGTGGGGAAAGCGCATTTGTA GGCCGCGGTGTGCGGGACCGGAGCCCGGCGCGGGCGGCGGCGGGGGTGGGGAAAGCGCATTTGTA T C ZNF782 Ensembl:ENSG00000196597 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:96854158..96854415 26863196 MeRIP-seq:(Medium) rs1431547914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036907 105480 RMVar_ID_105480 Human_SNP_ID_408119216 m1A Human chr9 + 97035578 97035578 97035578 AGGACGAATGGCCTGCATCCATAGCAACGGAGATGGGCCCCACAGTTGCGACTGCTTTCATCAGG AGGACGAATGGCCTGCATCCATAGCAACGGAGGTGGGCCCCACAGTTGCGACTGCTTTCATCAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:97032827..97036618 32194978 MeRIP-seq:(Medium) rs763750782 Functional Loss SNV dbSNP153 33..33 33 - - - 105481 RMVar_ID_105481 Human_SNP_ID_408119789 m1A Human chr9 + 97037321 97037321 97037321 CAATCCACAGATTTGGGAAGATCAAGAAACAGAGGCTCACGGAACACTTTCCCCTTCCTGAATTT CAATCCACAGATTTGGGAAGATCAAGAAACAGTGGCTCACGGAACACTTTCCCCTTCCTGAATTT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:97036717..97037516 32194978 MeRIP-seq:(Medium) rs1215886163 Functional Loss SNV dbSNP153 33..33 33 - - - 105482 RMVar_ID_105482 Human_SNP_ID_408120341 m1A Human chr9 - 97039114 97039112 97039114 CTGCACCAGACCGCGGACGTCTGTAATCTCAGAGGCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC CTGCACCAGACCGCGGACGTCTGTAATCTCAG__GCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC CCT C CTSV Ensembl:ENSG00000136943 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97039028..97039132 26863196 MeRIP-seq:(Medium) rs1223664375 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1065489,Human_Splice_Rec_1065517 105483 RMVar_ID_105483 Human_SNP_ID_408120343 m1A Human chr9 - 97039114 97039114 97039114 CTGCACCAGACCGCGGACGTCTGTAATCTCAGAGGCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC CTGCACCAGACCGCGGACGTCTGTAATCTCAGTGGCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC T A CTSV Ensembl:ENSG00000136943 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97039028..97039132 26863196 MeRIP-seq:(Medium) rs1028012539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1065489,Human_Splice_Rec_1065517 105484 RMVar_ID_105484 Human_SNP_ID_408120344 m1A Human chr9 - 97039114 97039114 97039114 CTGCACCAGACCGCGGACGTCTGTAATCTCAGAGGCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC CTGCACCAGACCGCGGACGTCTGTAATCTCAGGGGCTTGTTTGCTGAGGGTGCCTGCGCAGCTGC T C CTSV Ensembl:ENSG00000136943 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97039028..97039132 26863196 MeRIP-seq:(Medium) rs1028012539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1065489,Human_Splice_Rec_1065517 105485 RMVar_ID_105485 Human_SNP_ID_408143881 m1A Human chr9 + 97143823 97143823 97143823 TACTCCCCCTTCCTACTACCCACCACCCTCACACCACCCTACAGTCAACCTACTGCTCCGAACTT TACTCCCCCTTCCTACTACCCACCACCCTCACGCCACCCTACAGTCAACCTACTGCTCCGAACTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97143773..97143898 26863196 MeRIP-seq:(Medium) rs1234379235 Functional Loss SNV dbSNP153 33..33 33 - - - 105486 RMVar_ID_105486 Human_SNP_ID_408145266 m1A Human chr9 + 97149803 97149803 97149803 TCCATGAGAGCAGCCGCGGGGGCTAAACTTGCAAAGCCACAGGTGCACTGCCCTAGTAGAGGTTG TCCATGAGAGCAGCCGCGGGGGCTAAACTTGCTAAGCCACAGGTGCACTGCCCTAGTAGAGGTTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97149769..97149912 26863196 MeRIP-seq:(Medium) rs775561292 Functional Loss SNV dbSNP153 33..33 33 - - - 105487 RMVar_ID_105487 Human_SNP_ID_408161465 m1A Human chr9 + 97221421 97221421 97221421 CCCCAAACCCAAGATCCACCCCCAACCCCGCGATGTAGCTCAGAATCCGCGATCCAGCCCGGTCC CCCCAAACCCAAGATCCACCCCCAACCCCGCGGTGTAGCTCAGAATCCGCGATCCAGCCCGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97221389..97221455 26863196 MeRIP-seq:(Medium) rs957224312 Functional Loss SNV dbSNP153 33..33 33 - - - 105488 RMVar_ID_105488 Human_SNP_ID_408182387 m1A Human chr9 - 97309518 97309518 97309518 TTCTGCTGTCGGGGAGACATCACCTCCCCTTCAGGAGTCTCCACCTTCTTCATCATGGGTATCCT TTCTGCTGTCGGGGAGACATCACCTCCCCTTCGGGAGTCTCCACCTTCTTCATCATGGGTATCCT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:97309513..97309640 26863196 MeRIP-seq:(Medium) rs891186482 Functional Loss SNV dbSNP153 33..33 33 - - - 105489 RMVar_ID_105489 Human_SNP_ID_408185501 m1A Human chr9 - 97321872 97321872 97321872 CCCAGCCCTGTCTTGCCTCCGGGGCCCTGTACACTGTATCCCTGCTTGGAATGCCTCCTCCCTCT CCCAGCCCTGTCTTGCCTCCGGGGCCCTGTACGCTGTATCCCTGCTTGGAATGCCTCCTCCCTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97321830..97321898 26863196 MeRIP-seq:(Medium) rs756339879 Functional Loss SNV dbSNP153 33..33 33 - - - 105490 RMVar_ID_105490 Human_SNP_ID_408185502 m1A Human chr9 - 97321872 97321872 97321872 CCCAGCCCTGTCTTGCCTCCGGGGCCCTGTACACTGTATCCCTGCTTGGAATGCCTCCTCCCTCT CCCAGCCCTGTCTTGCCTCCGGGGCCCTGTACCCTGTATCCCTGCTTGGAATGCCTCCTCCCTCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97321830..97321898 26863196 MeRIP-seq:(Medium) rs756339879 Functional Loss SNV dbSNP153 33..33 33 - - - 105491 RMVar_ID_105491 Human_SNP_ID_408187765 m1A Human chr9 + 97330644 97330644 97330644 TCCCTGAATGAGGAGAATGTGAAGGGTCAAGGAGAAAAGAAGGAGGAGTCAGAGGAGGAAGATGA TCCCTGAATGAGGAGAATGTGAAGGGTCAAGGGGAAAAGAAGGAGGAGTCAGAGGAGGAAGATGA A G CCDC180,STRA6LP Ensembl:ENSG00000197816,Ensembl:ENSG00000255036 Protein coding,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:97330594..97330746 26863196 MeRIP-seq:(Medium) rs1045030239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5636446,Human_RBP_ID_26360851 RMVar_hsa_circ_19686,RMVar_hsa_circ_77490,RMVar_hsa_circ_258086,RMVar_hsa_circ_38613,RMVar_hsa_circ_258087,RMVar_hsa_circ_359362,RMVar_hsa_circ_40797,RMVar_hsa_circ_364733,RMVar_hsa_circ_72581 105492 RMVar_ID_105492 Human_SNP_ID_408190892 m1A Human chr9 - 97343294 97343294 97343294 AACACTAAAGTTGACTTGATATCATCAAATGGACTTGGGAATGCCAACCACAGGTTCCTTGATAT AACACTAAAGTTGACTTGATATCATCAAATGGGCTTGGGAATGCCAACCACAGGTTCCTTGATAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97343288..97343357 26863196 MeRIP-seq:(Medium) rs377441754 Functional Loss SNV dbSNP153 33..33 33 - - - 105493 RMVar_ID_105493 Human_SNP_ID_408210736 m1A Human chr9 + 97428419 97428419 97428419 CAGCTCTGAAAATCTATTTGAATTCACAAACGAATGAGCCATATTATAGTAACCTTCTACTGTGT CAGCTCTGAAAATCTATTTGAATTCACAAACGGATGAGCCATATTATAGTAACCTTCTACTGTGT A G TDRD7 Ensembl:ENSG00000196116 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:97428290..97428478 26863196 MeRIP-seq:(Medium) rs1374380829 Functional Loss SNV dbSNP153 33..33 33 - - - 105494 RMVar_ID_105494 Human_SNP_ID_408227902 m1A Human chr9 - 97501725 97501725 97501725 GGCGCGGGCGGCGGGCAGATGGACGCGGGCGGAGGCCGCGGTGCTCCGGCGGGCAGCGGGCGGGC GGCGCGGGCGGCGGGCAGATGGACGCGGGCGGGGGCCGCGGTGCTCCGGCGGGCAGCGGGCGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:97501678..97501802;chr9:97501679..97501804 26863196 MeRIP-seq:(Medium) rs1056192720 Functional Loss SNV dbSNP153 33..33 33 - - - 105495 RMVar_ID_105495 Human_SNP_ID_408244137 m1A Human chr9 - 97572351 97572351 97572351 CCCCTCCCATCCAGCCAGAACCATCTTCCCAGAGCACAGCACAGCCCACTTTCCCTAAACCTACC CCCCTCCCATCCAGCCAGAACCATCTTCCCAGGGCACAGCACAGCCCACTTTCCCTAAACCTACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97572319..97572569 26863196 MeRIP-seq:(Medium) rs1472026002 Functional Loss SNV dbSNP153 33..33 33 - - - 105496 RMVar_ID_105496 Human_SNP_ID_408249649 m1A Human chr9 + 97593796 97593796 97593796 AAGAGATAGGTTGATGGAGGAGGTCTAGAGGCATCCCTCTGGGGGTTCTAGGAGTATTAGGAAGT AAGAGATAGGTTGATGGAGGAGGTCTAGAGGCGTCCCTCTGGGGGTTCTAGGAGTATTAGGAAGT A G TMOD1 Ensembl:ENSG00000136842 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:97593784..97593938 26863196 MeRIP-seq:(Medium) rs1326536974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5226795 105497 RMVar_ID_105497 Human_SNP_ID_408252878 m1A Human chr9 + 97606312 97606312 97606312 AATTATATTAAAACAAAGACAAAAAAACCAAAACCCAATCATGACTCACCCAGCCTGACTTACGT AATTATATTAAAACAAAGACAAAAAAACCAAAGCCCAATCATGACTCACCCAGCCTGACTTACGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97606261..97606344 26863196 MeRIP-seq:(Medium) rs1480366848 Functional Loss SNV dbSNP153 33..33 33 - - - 105498 RMVar_ID_105498 Human_SNP_ID_408259054 m1A Human chr9 - 97633288 97633288 97633288 GAGGGCGGTGAGCAGTGACAATTGCTAGGCGGAGACAGTGCAGGGAAGAGAGACCTTAGAAAGGA GAGGGCGGTGAGCAGTGACAATTGCTAGGCGGGGACAGTGCAGGGAAGAGAGACCTTAGAAAGGA T C TSTD2 Ensembl:ENSG00000136925 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:97633220..97633346;chr9:97627531..97633360;chr9:97627496..97633337;chr9:97633243..97633332 26863196 MeRIP-seq:(Medium) rs1317219344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7880169 Human_Splice_Rec_1066299,Human_Splice_Rec_1066317 105499 RMVar_ID_105499 Human_SNP_ID_408259153 m1A Human chr9 + 97633525 97633525 97633525 GGCCGCCGGCACGACCCGCCTTCAGGCGTACGACGACCGCGGCCCGGGGGCTCTGAGTGGCCAAA GGCCGCCGGCACGACCCGCCTTCAGGCGTACGTCGACCGCGGCCCGGGGGCTCTGAGTGGCCAAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97633476..97633678 26863196 MeRIP-seq:(Medium) rs1291970898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258117,RMVar_hsa_circ_89529 105500 RMVar_ID_105500 Human_SNP_ID_408259191 m1A Human chr9 + 97633625 97633625 97633625 AGAGCGGAAGGCGGGAGAAAGAAGTAGCCGGCAGGCGGAGGCAGCCCGAGGGGGCGGTTGCATGT AGAGCGGAAGGCGGGAGAAAGAAGTAGCCGGCCGGCGGAGGCAGCCCGAGGGGGCGGTTGCATGT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:97633491..97633687 26863196 MeRIP-seq:(Medium) rs890553112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258117,RMVar_hsa_circ_89529 105501 RMVar_ID_105501 Human_SNP_ID_408259310 m1A Human chr9 + 97633874 97633874 97633874 CCGCCTGGCCTCTCGGTTCCGCGGCGCACCGGAGGGCAGCATGTCGCGGCGGCGGCACAGCGACG CCGCCTGGCCTCTCGGTTCCGCGGCGCACCGGCGGGCAGCATGTCGCGGCGGCGGCACAGCGACG A C NCBP1 Ensembl:ENSG00000136937 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:97633825..97633914 26863196 MeRIP-seq:(Medium) rs1358095366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036262,Human_RBP_ID_8930121,Human_RBP_ID_9315600 Human_Splice_Rec_1066355,Human_Splice_Rec_1066367,Human_Splice_Rec_1066411 RMVar_hsa_circ_258117,RMVar_hsa_circ_89529 105502 RMVar_ID_105502 Human_SNP_ID_408273290 m1A Human chr9 - 97690080 97690080 97690080 GGGTCATGAGTCAAGGAATGCAGGCAGCCTATAGAAGCTGGAAAAGGCAAGGAGATGGATTCTTG GGGTCATGAGTCAAGGAATGCAGGCAGCCTATGGAAGCTGGAAAAGGCAAGGAGATGGATTCTTG T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97690077..97690183 26863196 MeRIP-seq:(Medium) rs1224764690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 105503 RMVar_ID_105503 Human_SNP_ID_408273294 m1A Human chr9 - 97690091 97690091 97690091 GATGGAGGAAGGGGTCATGAGTCAAGGAATGCAGGCAGCCTATAGAAGCTGGAAAAGGCAAGGAG GATGGAGGAAGGGGTCATGAGTCAAGGAATGCGGGCAGCCTATAGAAGCTGGAAAAGGCAAGGAG T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:97690087..97690158 26863196 MeRIP-seq:(Medium) rs1353487967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16519133 RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 105504 RMVar_ID_105504 Human_SNP_ID_408273295 m1A Human chr9 + 97690102 97690102 97690102 TTCCAGCTTCTATAGGCTGCCTGCATTCCTTGACTCATGACCCCTTCCTCCATCTTCATAGCCAG TTCCAGCTTCTATAGGCTGCCTGCATTCCTTGCCTCATGACCCCTTCCTCCATCTTCATAGCCAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97690100..97690207 26863196 MeRIP-seq:(Medium) rs1225512148 Functional Loss SNV dbSNP153 33..33 33 - - - 105505 RMVar_ID_105505 Human_SNP_ID_408274175 m1A Human chr9 - 97693743 97693742 97693744 TTACTTACTTTTGTAGGCATGGCTAATGTAAAAGCAGCCCCAAAGATAATTGACACAGGAGGAGG TTACTTACTTTTGTAGGCATGGCTAATGTAA__GCAGCCCCAAAGATAATTGACACAGGAGGAGG CTT C XPA Ensembl:ENSG00000136936 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:97693676..97693801;chr9:97693651..97693822 26863196 MeRIP-seq:(Medium) rs1192717307 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1066428,Human_Splice_Rec_1066429,Human_Splice_Rec_1066440,Human_Splice_Rec_1066441,Human_Splice_Rec_1066452,Human_Splice_Rec_1066453 RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 105506 RMVar_ID_105506 Human_SNP_ID_408274983 m1A Human chr9 - 97697279 97697279 97697279 TCCTCGGAGTGGGCCAGAGATGGCGGCGGCCGACGGGGCTTTGCCGGAGGCGGCGGCTTTAGAGC TCCTCGGAGTGGGCCAGAGATGGCGGCGGCCGTCGGGGCTTTGCCGGAGGCGGCGGCTTTAGAGC T A XPA Ensembl:ENSG00000136936 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:97693747..97697384;chr9:97697082..97697385;chr9:97697084..97697376;chr9:97693648..97697376 26863196 MeRIP-seq:(Medium) rs905489379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036263,Human_RBP_ID_23120891,Human_RBP_ID_27832506 Human_Splice_Rec_1066451 105507 RMVar_ID_105507 Human_SNP_ID_408274984 m1A Human chr9 - 97697279 97697279 97697279 TCCTCGGAGTGGGCCAGAGATGGCGGCGGCCGACGGGGCTTTGCCGGAGGCGGCGGCTTTAGAGC TCCTCGGAGTGGGCCAGAGATGGCGGCGGCCGCCGGGGCTTTGCCGGAGGCGGCGGCTTTAGAGC T G XPA Ensembl:ENSG00000136936 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:97693747..97697384;chr9:97697082..97697385;chr9:97697084..97697376;chr9:97693648..97697376 26863196 MeRIP-seq:(Medium) rs905489379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036263,Human_RBP_ID_23120891,Human_RBP_ID_27832506 Human_Splice_Rec_1066451 105508 RMVar_ID_105508 Human_SNP_ID_408310666 m1A Human chr9 - 97853256 97853256 97853256 GCGTGGGTCTCCAGCCCTGCGGACCGCTGGCGAGGCGCTCCCCTGCACACACCGGACCGGCTCCT GCGTGGGTCTCCAGCCCTGCGGACCGCTGGCGGGGCGCTCCCCTGCACACACCGGACCGGCTCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97853247..97853573 26863196 MeRIP-seq:(Medium) rs765969324 Functional Loss SNV dbSNP153 33..33 33 - - - 105509 RMVar_ID_105509 Human_SNP_ID_408310672 m1A Human chr9 + 97853271 97853271 97853271 GTGTGCAGGGGAGCGCCTCGCCAGCGGTCCGCAGGGCTGGAGACCCACGCCGTGGAGAGGACCAG GTGTGCAGGGGAGCGCCTCGCCAGCGGTCCGCCGGGCTGGAGACCCACGCCGTGGAGAGGACCAG A C FOXE1 Ensembl:ENSG00000178919 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97853267..97853473 26863196 MeRIP-seq:(Medium) rs13302470 Functional Loss SNV dbSNP153 33..33 33 - - - 105510 RMVar_ID_105510 Human_SNP_ID_408310673 m1A Human chr9 + 97853271 97853271 97853271 GTGTGCAGGGGAGCGCCTCGCCAGCGGTCCGCAGGGCTGGAGACCCACGCCGTGGAGAGGACCAG GTGTGCAGGGGAGCGCCTCGCCAGCGGTCCGCGGGGCTGGAGACCCACGCCGTGGAGAGGACCAG A G FOXE1 Ensembl:ENSG00000178919 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97853267..97853473 26863196 MeRIP-seq:(Medium) rs13302470 Functional Loss SNV dbSNP153 33..33 33 - - - 105511 RMVar_ID_105511 Human_SNP_ID_408310975 m1A Human chr9 + 97854215 97854215 97854215 ACCGCGACAACCCCAAAAAGTGGCAGAACAGCATCCGCCACAACCTCACACTCAACGACTGCTTC ACCGCGACAACCCCAAAAAGTGGCAGAACAGCGTCCGCCACAACCTCACACTCAACGACTGCTTC A G FOXE1 Ensembl:ENSG00000178919 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97854164..97854247 26863196 MeRIP-seq:(Medium) rs1478308136 Functional Loss SNV dbSNP153 33..33 33 - - - 105512 RMVar_ID_105512 Human_SNP_ID_408311136 m1A Human chr9 + 97854452 97854452 97854452 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCATCTTCCCAGGCGCGGTGCCCGCCGCGCGCCCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGTCTTCCCAGGCGCGGTGCCCGCCGCGCGCCCC A G FOXE1 Ensembl:ENSG00000178919 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:97854390..97854490 26863196 MeRIP-seq:(Medium) rs1564089195 Functional Loss SNV dbSNP153 33..33 33 - - - 105513 RMVar_ID_105513 Human_SNP_ID_408324139 m1A Human chr9 + 97907719 97907719 97907719 CTGCCTTTTACTTCTCCCAAGATCAAAACTCAAGTCCTTACAATGGCCTATAAAACCCTTAGGTG CTGCCTTTTACTTCTCCCAAGATCAAAACTCACGTCCTTACAATGGCCTATAAAACCCTTAGGTG A C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:97907717..97907813 26863196 MeRIP-seq:(Medium) rs1309857092 Functional Loss SNV dbSNP153 33..33 33 - - - 105514 RMVar_ID_105514 Human_SNP_ID_408324809 m1A Human chr9 + 97909997 97909997 97909997 GAACTGAGCTGCCCAAGGTCCATCTCGGCATGAGGAGTAAACCGCACTTCTAAAGTGGCCACAGG GAACTGAGCTGCCCAAGGTCCATCTCGGCATGCGGAGTAAACCGCACTTCTAAAGTGGCCACAGG A C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:97904982..97910049 32194978 MeRIP-seq:(Medium) rs759579139 Functional Loss SNV dbSNP153 33..33 33 - - - 105515 RMVar_ID_105515 Human_SNP_ID_408326461 m1A Human chr9 - 97916335 97916335 97916335 ATAACTTTTTACCTAATTTTCTCCTGTAGGGAATCTTTTAACTGAGCCAGTCGGCTACTTGGAAT ATAACTTTTTACCTAATTTTCTCCTGTAGGGAGTCTTTTAACTGAGCCAGTCGGCTACTTGGAAT T C TRMO Ensembl:ENSG00000136932 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:97916317..97916413 26863410 MeRIP-seq:(Medium) rs760169725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1066522,Human_Splice_Rec_1066532,Human_Splice_Rec_1066548,Human_Splice_Rec_1066562 RMVar_hsa_circ_112372,RMVar_hsa_circ_379099,RMVar_hsa_circ_258153 105516 RMVar_ID_105516 Human_SNP_ID_408328209 m1A Human chr9 + 97922475 97922475 97922475 GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGACTCCTCCAAGCCGCGCATGGCTACTGGTTGCT GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGCCTCCTCCAAGCCGCGCATGGCTACTGGTTGCT A C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97922384..97922515 26863196 MeRIP-seq:(Medium) rs3183927 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14070,GWAS_ID_14071,GWAS_ID_14072,GWAS_ID_14073,GWAS_ID_14074,GWAS_ID_14075,GWAS_ID_14076,GWAS_ID_14077,GWAS_ID_14078,GWAS_ID_14079,GWAS_ID_14080,GWAS_ID_14081,GWAS_ID_14082,GWAS_ID_14083,GWAS_ID_14084,GWAS_ID_14085,GWAS_ID_14086,GWAS_ID_14087,GWAS_ID_14088,GWAS_ID_14089,GWAS_ID_14090,GWAS_ID_14091,GWAS_ID_14092 105517 RMVar_ID_105517 Human_SNP_ID_408328210 m1A Human chr9 + 97922475 97922475 97922475 GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGACTCCTCCAAGCCGCGCATGGCTACTGGTTGCT GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGGCTCCTCCAAGCCGCGCATGGCTACTGGTTGCT A G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97922384..97922515 26863196 MeRIP-seq:(Medium) rs3183927 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_14070,GWAS_ID_14071,GWAS_ID_14072,GWAS_ID_14073,GWAS_ID_14074,GWAS_ID_14075,GWAS_ID_14076,GWAS_ID_14077,GWAS_ID_14078,GWAS_ID_14079,GWAS_ID_14080,GWAS_ID_14081,GWAS_ID_14082,GWAS_ID_14083,GWAS_ID_14084,GWAS_ID_14085,GWAS_ID_14086,GWAS_ID_14087,GWAS_ID_14088,GWAS_ID_14089,GWAS_ID_14090,GWAS_ID_14091,GWAS_ID_14092 105518 RMVar_ID_105518 Human_SNP_ID_408342691 m1A Human chr9 + 97983430 97983430 97983430 CTCGCCTGCCCGCACGCCGCCCGCCACCCAGGACCGCGCCGCCGGCCTCCGCCGCTAGCAAACCC CTCGCCTGCCCGCACGCCGCCCGCCACCCAGGGCCGCGCCGCCGGCCTCCGCCGCTAGCAAACCC A G ANP32B Ensembl:ENSG00000136938 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:97983213..97983525 26863410 MeRIP-seq:(Medium) rs976361710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256667,Human_RBP_ID_798237,Human_RBP_ID_5003461,Human_RBP_ID_9338978,Human_RBP_ID_17437107,Human_RBP_ID_18901160,Human_RBP_ID_22534465 105519 RMVar_ID_105519 Human_SNP_ID_408342705 m1A Human chr9 + 97983459 97983459 97983459 AGGACCGCGCCGCCGGCCTCCGCCGCTAGCAAACCCTTCCGACGGCCCTCGCTGCGCAAGCCGGG AGGACCGCGCCGCCGGCCTCCGCCGCTAGCAACCCCTTCCGACGGCCCTCGCTGCGCAAGCCGGG A C ANP32B Ensembl:ENSG00000136938 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:97983344..97983580 26863196 MeRIP-seq:(Medium) rs972303333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92488,Human_RBP_ID_707126,Human_RBP_ID_5036266,Human_RBP_ID_5453943,Human_RBP_ID_5481529,Human_RBP_ID_5515387,Human_RBP_ID_9338979,Human_RBP_ID_17437108,Human_RBP_ID_22333805,Human_RBP_ID_22534465,Human_RBP_ID_27128191 105520 RMVar_ID_105520 Human_SNP_ID_408342719 m1A Human chr9 + 97983492 97983492 97983492 CCCTTCCGACGGCCCTCGCTGCGCAAGCCGGGACGCCTCTCCCCCCTCCGCCCCCGCCGCGGAAA CCCTTCCGACGGCCCTCGCTGCGCAAGCCGGGCCGCCTCTCCCCCCTCCGCCCCCGCCGCGGAAA A C ANP32B Ensembl:ENSG00000136938 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:97983301..97983525 26863196 MeRIP-seq:(Medium) rs1388238302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92488,Human_RBP_ID_798238,Human_RBP_ID_5036266,Human_RBP_ID_5453944,Human_RBP_ID_5481530,Human_RBP_ID_5515388,Human_RBP_ID_8275070,Human_RBP_ID_8692961,Human_RBP_ID_9338979,Human_RBP_ID_17437110,Human_RBP_ID_18901161,Human_RBP_ID_22534465,Human_RBP_ID_23088861,Human_RBP_ID_24275412,Human_RBP_ID_26240794,Human_RBP_ID_26834075 105521 RMVar_ID_105521 Human_SNP_ID_408342786 m1A Human chr9 + 97983598 97983598 97983598 AGAGGAGGATCCACCTGGAGCTGAGGAACCGGACCCCGGCAGCTGTAAGCAGAGACCCCTCTGGG AGAGGAGGATCCACCTGGAGCTGAGGAACCGGGCCCCGGCAGCTGTAAGCAGAGACCCCTCTGGG A G ANP32B Ensembl:ENSG00000136938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:97983289..97984643 32194978 MeRIP-seq:(Medium) rs1017983718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256668,Human_RBP_ID_798239,Human_RBP_ID_1700443,Human_RBP_ID_2058621,Human_RBP_ID_3889455,Human_RBP_ID_5003467,Human_RBP_ID_7880594,Human_RBP_ID_8275073,Human_RBP_ID_9407089,Human_RBP_ID_16519839,Human_RBP_ID_18126084,Human_RBP_ID_18545067,Human_RBP_ID_19145335,Human_RBP_ID_23094604,Human_RBP_ID_26360885,Human_RBP_ID_27833219 Human_Splice_Rec_1066577 105522 RMVar_ID_105522 Human_SNP_ID_408348769 m1A Human chr9 + 98005124 98005124 98005124 CCAGGAAGCACCTGACTCAGATGCCGAGGTGGATGGTGTGGATGAAGAGGAGGAGGACGAAGGTG CCAGGAAGCACCTGACTCAGATGCCGAGGTGGGTGGTGTGGATGAAGAGGAGGAGGACGAAGGTG A G ANP32B Ensembl:ENSG00000136938 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:98005076..98005269 26863196 MeRIP-seq:(Medium) rs1401408342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707137,Human_RBP_ID_797477,Human_RBP_ID_847214,Human_RBP_ID_1057222,Human_RBP_ID_3889484,Human_RBP_ID_7880711,Human_RBP_ID_8923970,Human_RBP_ID_22837422,Human_RBP_ID_23094317,Human_RBP_ID_24275429,Human_RBP_ID_24549610 Human_Splice_Rec_1066583 RMVar_hsa_circ_21299,RMVar_hsa_circ_86610,RMVar_hsa_circ_332987,RMVar_hsa_circ_367280,RMVar_hsa_circ_258156,RMVar_hsa_circ_258157,RMVar_hsa_circ_353735 105523 RMVar_ID_105523 Human_SNP_ID_408348774 m1A Human chr9 + 98005139 98005137 98005140 CTCAGATGCCGAGGTGGATGGTGTGGATGAAGAGGAGGAGGACGAAGGTGAGTAGGCTCAGCATC CTCAGATGCCGAGGTGGATGGTGTGGATGAA___GAGGAGGACGAAGGTGAGTAGGCTCAGCATC AGAG A ANP32B Ensembl:ENSG00000136938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:98004949..98005175 32194978 MeRIP-seq:(Medium) rs773305793 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_707138,Human_RBP_ID_847214,Human_RBP_ID_3889484,Human_RBP_ID_7880711,Human_RBP_ID_16520511,Human_RBP_ID_19143577,Human_RBP_ID_23094317,Human_RBP_ID_23117218,Human_RBP_ID_23120842,Human_RBP_ID_24275429,Human_RBP_ID_24549610 Human_Splice_Rec_1066583 RMVar_hsa_circ_21299,RMVar_hsa_circ_86610,RMVar_hsa_circ_332987,RMVar_hsa_circ_367280,RMVar_hsa_circ_258156,RMVar_hsa_circ_258157,RMVar_hsa_circ_353735 105524 RMVar_ID_105524 Human_SNP_ID_408350363 m1A Human chr9 + 98011347 98011338 98011347 GAGGAGTTTGATGAAGAAGATGATGAAGATGAAGATGTAGAAGGGGATGAGGACGACGATGAAGT GAGGAGTTTGATGAAGAAGATGAT_________GATGTAGAAGGGGATGAGGACGACGATGAAGT TGAAGATGAA T ANP32B Ensembl:ENSG00000136938 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:98011177..98015494 26863196 MeRIP-seq:(Medium) rs1373982700 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_91246,Human_RBP_ID_219005,Human_RBP_ID_707142,Human_RBP_ID_1057223,Human_RBP_ID_1700462,Human_RBP_ID_2058645,Human_RBP_ID_3180075,Human_RBP_ID_5003502,Human_RBP_ID_5633460,Human_RBP_ID_7880739,Human_RBP_ID_8275074,Human_RBP_ID_9351751,Human_RBP_ID_16520678,Human_RBP_ID_18140548,Human_RBP_ID_18414501,Human_RBP_ID_18541875,Human_RBP_ID_18901184,Human_RBP_ID_22013030,Human_RBP_ID_22118765,Human_RBP_ID_22333842,Human_RBP_ID_22837423,Human_RBP_ID_23094326,Human_RBP_ID_23117221,Human_RBP_ID_23120844,Human_RBP_ID_24275444,Human_RBP_ID_24549615,Human_RBP_ID_26360389,Human_RBP_ID_27540620,Human_RBP_ID_27570107,Human_RBP_ID_27832524 Human_Splice_Rec_1066584,Human_Splice_Rec_1066585 RMVar_hsa_circ_86610,RMVar_hsa_circ_367280,RMVar_hsa_circ_258156 105525 RMVar_ID_105525 Human_SNP_ID_408350367 m1A Human chr9 - 98011350 98011350 98011350 CTGACTTCATCGTCGTCCTCATCCCCTTCTACATCTTCATCTTCATCATCTTCTTCATCAAACTC CTGACTTCATCGTCGTCCTCATCCCCTTCTACGTCTTCATCTTCATCATCTTCTTCATCAAACTC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:98011301..98011400 26863196 MeRIP-seq:(Medium) rs1161942046 Functional Loss SNV dbSNP153 33..33 33 - - - 105526 RMVar_ID_105526 Human_SNP_ID_408361370 m1A Human chr9 + 98056772 98056772 98056772 GAGTAGAGGCGGCGGCGGCGGCGGCCGGACCCAGACTGGTAGTGAGGCTTTGGACCCCGAGCCGC GAGTAGAGGCGGCGGCGGCGGCGGCCGGACCCGGACTGGTAGTGAGGCTTTGGACCCCGAGCCGC A G NANS Ensembl:ENSG00000095380 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:98056753..98056841 26863410 MeRIP-seq:(Medium) rs1366347019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036267,Human_RBP_ID_5329556,Human_RBP_ID_9338980,Human_RBP_ID_22119656,Human_RBP_ID_22466420,Human_RBP_ID_27368580 105527 RMVar_ID_105527 Human_SNP_ID_408361411 m1A Human chr9 - 98056832 98056832 98056832 CACGGGTGTTGCCCGCCCACCCAGCGCCCGGGACACAGCTCCAGCTCCAGCGGCATTGCAGCGGC CACGGGTGTTGCCCGCCCACCCAGCGCCCGGGGCACAGCTCCAGCTCCAGCGGCATTGCAGCGGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:98056750..98056837 26863410 MeRIP-seq:(Medium) rs775230449 Functional Loss SNV dbSNP153 33..33 33 - - - 105528 RMVar_ID_105528 Human_SNP_ID_408361416 m1A Human chr9 - 98056842 98056842 98056842 AATGATGAAGCACGGGTGTTGCCCGCCCACCCAGCGCCCGGGACACAGCTCCAGCTCCAGCGGCA AATGATGAAGCACGGGTGTTGCCCGCCCACCCCGCGCCCGGGACACAGCTCCAGCTCCAGCGGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr9:98056701..98056975;chr9:98056751..98056900 26863196,26863410 MeRIP-seq:(Medium) rs1316408115 Functional Loss SNV dbSNP153 33..33 33 - - - 105529 RMVar_ID_105529 Human_SNP_ID_408361417 m1A Human chr9 - 98056842 98056842 98056842 AATGATGAAGCACGGGTGTTGCCCGCCCACCCAGCGCCCGGGACACAGCTCCAGCTCCAGCGGCA AATGATGAAGCACGGGTGTTGCCCGCCCACCCGGCGCCCGGGACACAGCTCCAGCTCCAGCGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr9:98056701..98056975;chr9:98056751..98056900 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 105530 RMVar_ID_105530 Human_SNP_ID_408362383 m1A Human chr9 + 98060859 98060859 98060859 TTCAAGTTTAATCGGAAAGCCTTGGAGAGGCCATACACCTCGAAGCATTCCTGGGGGAAGACGTA TTCAAGTTTAATCGGAAAGCCTTGGAGAGGCCGTACACCTCGAAGCATTCCTGGGGGAAGACGTA A G NANS Ensembl:ENSG00000095380 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:98056776..98061027 32194978 MeRIP-seq:(Medium) rs749041746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407102,Human_RBP_ID_18141161,Human_RBP_ID_22467350 Human_Splice_Rec_1066600,Human_Splice_Rec_1066610,Human_Splice_Rec_1066618 RMVar_hsa_circ_38903,RMVar_hsa_circ_45668,RMVar_hsa_circ_329342,RMVar_hsa_circ_258162 105531 RMVar_ID_105531 Human_SNP_ID_408362413 m1A Human chr9 - 98060925 98060925 98060925 TCGGCGTACCTCTGCAGCTCCCTGTACTGGTCATGGCTGAACTCCAGATGTCGTTTGTGCTCCCC TCGGCGTACCTCTGCAGCTCCCTGTACTGGTCGTGGCTGAACTCCAGATGTCGTTTGTGCTCCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:98060876..98061000 26863196 MeRIP-seq:(Medium) rs757033554 Functional Loss SNV dbSNP153 33..33 33 - - - 105532 RMVar_ID_105532 Human_SNP_ID_408365799 m1A Human chr9 + 98075317 98075315 98075317 ACCACAAAAGAAAAGAAAAAGATGGAAGGGGAAAAGAGAAGAGTTAAAAATAAAGCAGAGGAAGA ACCACAAAAGAAAAGAAAAAGATGGAAGGGG__AAGAGAAGAGTTAAAAATAAAGCAGAGGAAGA GAA G NANS Ensembl:ENSG00000095380 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:98075315..98075380 26863196 MeRIP-seq:(Medium) rs573564925 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_38903,RMVar_hsa_circ_45668 105533 RMVar_ID_105533 Human_SNP_ID_408365802 m1A Human chr9 - 98075335 98075335 98075335 CTTCACCTTTCTCACTGCTCTTCCTCTGCTTTATTTTTAACTCTTCTCTTTTCCCCTTCCATCTT CTTCACCTTTCTCACTGCTCTTCCTCTGCTTTGTTTTTAACTCTTCTCTTTTCCCCTTCCATCTT T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:98075332..98075584 26863196 MeRIP-seq:(Medium) rs1368676331 Functional Loss SNV dbSNP153 33..33 33 - - - 105534 RMVar_ID_105534 Human_SNP_ID_408366239 m1A Human chr9 + 98076976 98076976 98076976 GAATGTTCCATTTTTCAAAGTTGGATCTGGAGACACTAATAATTTTCCTTATCTGGAAAAGACAG GAATGTTCCATTTTTCAAAGTTGGATCTGGAGTCACTAATAATTTTCCTTATCTGGAAAAGACAG A T NANS Ensembl:ENSG00000095380 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:98076895..98077025 32194978 MeRIP-seq:(Medium) rs908466458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1057230,Human_RBP_ID_1247588,Human_RBP_ID_2058665,Human_RBP_ID_18126128,Human_RBP_ID_22466924,Human_RBP_ID_22776494,Human_RBP_ID_26834088,Human_RBP_ID_27780950 Human_Splice_Rec_1066602,Human_Splice_Rec_1066603,Human_Splice_Rec_1066614,Human_Splice_Rec_1066615,Human_Splice_Rec_1066619,Human_Splice_Rec_1066625 Human_miRNA_ID_1977354,Human_miRNA_ID_3120842 RMVar_hsa_circ_104353,RMVar_hsa_circ_38903,RMVar_hsa_circ_45668,RMVar_hsa_circ_278589,RMVar_hsa_circ_106803,RMVar_hsa_circ_258163,RMVar_hsa_circ_258164,RMVar_hsa_circ_287638,RMVar_hsa_circ_258165,RMVar_hsa_circ_258166 105535 RMVar_ID_105535 Human_SNP_ID_408366523 m1A Human chr9 - 98078178 98078178 98078178 AGATCACCATTGGGCGACCTGAGTAATCCAGCACCAACACCATCAGCACTTTCTCTTTAGAGGTT AGATCACCATTGGGCGACCTGAGTAATCCAGCCCCAACACCATCAGCACTTTCTCTTTAGAGGTT T G TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:98078176..98078300 26863196 MeRIP-seq:(Medium) rs1257002253 Functional Loss SNV dbSNP153 33..33 33 - - - 105536 RMVar_ID_105536 Human_SNP_ID_408367206 m1A Human chr9 + 98080927 98080927 98080927 TGGCTCTGGGGGCCAAGGTGTTGGAACGTCACATAACTTTGGACAAGACCTGGAAGGGGAGTGAC TGGCTCTGGGGGCCAAGGTGTTGGAACGTCACGTAACTTTGGACAAGACCTGGAAGGGGAGTGAC A G NANS Ensembl:ENSG00000095380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:98080876..98081033 26863196 MeRIP-seq:(Medium) rs1258323750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5003553,Human_RBP_ID_9230676,Human_RBP_ID_22466160,Human_RBP_ID_23094615 RMVar_hsa_circ_106803,RMVar_hsa_circ_258166,RMVar_hsa_circ_102360,RMVar_hsa_circ_258167 105537 RMVar_ID_105537 Human_SNP_ID_408367782 m1A Human chr9 + 98082973 98082971 98082974 TCCTCCTGAAGACATCTTTAATCTAGTGGGCAAGAAGGTCCTGGTCACTGTTGAAGAGGATGACA TCCTCCTGAAGACATCTTTAATCTAGTGGGC___AAGGTCCTGGTCACTGTTGAAGAGGATGACA CAAG C NANS Ensembl:ENSG00000095380 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:98082875..98083025;chr9:98082146..98083025 32194978 MeRIP-seq:(Medium) rs1234139229 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_846665,Human_RBP_ID_961462,Human_RBP_ID_3974631,Human_RBP_ID_5003571,Human_RBP_ID_5124163,Human_RBP_ID_7880862,Human_RBP_ID_9407106,Human_RBP_ID_16521261,Human_RBP_ID_17715466,Human_RBP_ID_18126138,Human_RBP_ID_18901216,Human_RBP_ID_22466161 Human_miRNA_ID_2586906 RMVar_hsa_circ_106803,RMVar_hsa_circ_258166,RMVar_hsa_circ_102360,RMVar_hsa_circ_258167 105538 RMVar_ID_105538 Human_SNP_ID_408371237 m1A Human chr9 + 98096637 98096637 98096637 TCCCAGCCCTTCATCTCTCAGGCCAGAAACCCAGGCATCATCTGGGGATTCCTCCTACCCATTCT TCCCAGCCCTTCATCTCTCAGGCCAGAAACCCGGGCATCATCTGGGGATTCCTCCTACCCATTCT A G L13712-001,RF00017-4590,RF00017-4531 RNACentral:URS0000334622,RNACentral:URS0000965567,RNACentral:URS000098F531 misc_RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:98096636..98096813 26863196 MeRIP-seq:(Medium) rs1317627075 Functional Loss SNV dbSNP153 33..33 33 - - - 105539 RMVar_ID_105539 Human_SNP_ID_408376487 m1A Human chr9 - 98118889 98118889 98118889 CGGCCGAGGAGGGGGCGTGCCTGGCCGTGGCCAGTGGCGGGTTACAACCTGGAAACCAAAGGTGC CGGCCGAGGAGGGGGCGTGCCTGGCCGTGGCCGGTGGCGGGTTACAACCTGGAAACCAAAGGTGC T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:98118887..98118974 26863196 MeRIP-seq:(Medium) rs984252683 Functional Loss SNV dbSNP153 33..33 33 - - - 105540 RMVar_ID_105540 Human_SNP_ID_408386964 m1A Human chr9 - 98159490 98159490 98159490 GGAGATGCAAGAGCAGGTGCTGGGGAAGCTGGAAGGTGCCGTTTAGATGAGCTAGAAGAAAAGAA GGAGATGCAAGAGCAGGTGCTGGGGAAGCTGGGAGGTGCCGTTTAGATGAGCTAGAAGAAAAGAA T C CORO2A Ensembl:ENSG00000106789 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:98159484..98159567 26863196 MeRIP-seq:(Medium) rs11999011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100499,RMVar_hsa_circ_258182 105541 RMVar_ID_105541 Human_SNP_ID_408394968 m1A Human chr9 - 98192611 98192611 98192611 CGCCGGGAGTCGGCGGGCGGCGAGGAGCGCGGAGCCGGAGCTGGACGCCGCCGCCGCCACCGCCA CGCCGGGAGTCGGCGGGCGGCGAGGAGCGCGGCGCCGGAGCTGGACGCCGCCGCCGCCACCGCCA T G CORO2A Ensembl:ENSG00000106789 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:98192532..98192653;chr9:98192515..98192614 26863196 MeRIP-seq:(Medium) rs1331589225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036271 Human_Splice_Rec_1066697 RMVar_hsa_circ_100499,RMVar_hsa_circ_258182 105542 RMVar_ID_105542 Human_SNP_ID_408402009 m1A Human chr9 - 98221056 98221056 98221056 CCGGCGGGTGGAGGCCCTGGAGCAGGAGCGGGAGAGCCTGGCGCACACAGCGAGCCTGCGGGAGC CCGGCGGGTGGAGGCCCTGGAGCAGGAGCGGGGGAGCCTGGCGCACACAGCGAGCCTGCGGGAGC T C TBC1D2 Ensembl:ENSG00000095383 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:98221006..98221117;chr9:98220943..98221192 26863196 MeRIP-seq:(Medium) rs550551058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83408,RMVar_hsa_circ_35901,RMVar_hsa_circ_50091,RMVar_hsa_circ_258183,RMVar_hsa_circ_7861,RMVar_hsa_circ_44466 105543 RMVar_ID_105543 Human_SNP_ID_408524199 m1A Human chr9 - 98736389 98736389 98736389 TAGTCATGTTGTTCCCTTTGCTCGGGATGCCCACTTCACGTCGACGGCATTCATTGGTAGTACTT TAGTCATGTTGTTCCCTTTGCTCGGGATGCCCGCTTCACGTCGACGGCATTCATTGGTAGTACTT T C ANKS6 Ensembl:ENSG00000165138 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:98736341..98736473 26863196 MeRIP-seq:(Medium) rs111855758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18901254 105544 RMVar_ID_105544 Human_SNP_ID_408536107 m1A Human chr9 + 98784028 98784028 98784028 TGTCCTGCTTGTCAACATCCGCGTGCCTCTCCACCAGCAGCTGCACCAGAGCCAGCTGCCCCGTA TGTCCTGCTTGTCAACATCCGCGTGCCTCTCCCCCAGCAGCTGCACCAGAGCCAGCTGCCCCGTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:98783978..98784071 26863196 MeRIP-seq:(Medium) rs1227553995 Functional Loss SNV dbSNP153 33..33 33 - - - 105545 RMVar_ID_105545 Human_SNP_ID_408537843 m1A Human chr9 - 98790278 98790278 98790278 ACGCAGCCCGGACCGTGGGCTGGAGCCCGCTGATGCTGGCCGCACTCACTGGGCGGCTTGGAGTG ACGCAGCCCGGACCGTGGGCTGGAGCCCGCTGGTGCTGGCCGCACTCACTGGGCGGCTTGGAGTG T C ANKS6 Ensembl:ENSG00000165138 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:98790265..98790517 26863196 MeRIP-seq:(Medium) rs1420726671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23094469 RMVar_hsa_circ_35916,RMVar_hsa_circ_363023,RMVar_hsa_circ_29237 105546 RMVar_ID_105546 Human_SNP_ID_408539536 m1A Human chr9 - 98796424 98796424 98796424 GCTGCTGCGCGCGTGTGACCAGGGCGACACGGAGACGGCGCGGCGGCTGCTGGAGCCGGGGGCGG GCTGCTGCGCGCGTGTGACCAGGGCGACACGGCGACGGCGCGGCGGCTGCTGGAGCCGGGGGCGG T G ANKS6 Ensembl:ENSG00000165138 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:98796380..98796513 26863196 MeRIP-seq:(Medium) rs1226806353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036272,Human_RBP_ID_5227711,Human_RBP_ID_17175208,Human_RBP_ID_23094733 105547 RMVar_ID_105547 Human_SNP_ID_408542256 m1A Human chr9 + 98807754 98807754 98807754 GCGCTGCCCGCGGGAACTGCGGCGCGGCCGGGAGGCGCTGTTGGTGCTCCTGGCGCTACTGGCGT GCGCTGCCCGCGGGAACTGCGGCGCGGCCGGGCGGCGCTGTTGGTGCTCCTGGCGCTACTGGCGT A C GALNT12 Ensembl:ENSG00000119514 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:98807705..98807818;chr9:98807708..98807829 26863196 MeRIP-seq:(Medium) rs1233215782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036273 105548 RMVar_ID_105548 Human_SNP_ID_408574878 m1A Human chr9 - 98944038 98944035 98944038 TGGTGCCATCTCGCGGGTCTGCGGAGCCCCGGAAGGCGCGCGGCTAGTCGAGCAGAGCGTTGGAG TGGTGCCATCTCGCGGGTCTGCGGAGCCCCGG___GCGCGCGGCTAGTCGAGCAGAGCGTTGGAG CCTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:98943851..98944120 26863196 MeRIP-seq:(Medium) rs754932175 Functional Loss DEL dbSNP153 33..35 33 - - - 105549 RMVar_ID_105549 Human_SNP_ID_408574881 m1A Human chr9 - 98944038 98944038 98944038 TGGTGCCATCTCGCGGGTCTGCGGAGCCCCGGAAGGCGCGCGGCTAGTCGAGCAGAGCGTTGGAG TGGTGCCATCTCGCGGGTCTGCGGAGCCCCGGGAGGCGCGCGGCTAGTCGAGCAGAGCGTTGGAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:98943851..98944120 26863196 MeRIP-seq:(Medium) rs1375651910 Functional Loss SNV dbSNP153 33..33 33 - - - 105550 RMVar_ID_105550 Human_SNP_ID_408574970 m1A Human chr9 - 98944225 98944225 98944225 TGCTTACCTGTCGCACCGCGGGTCTGGGTGACAGCAGGGAGGGGCGTGGAGACCGAGAGCAGCAT TGCTTACCTGTCGCACCGCGGGTCTGGGTGACGGCAGGGAGGGGCGTGGAGACCGAGAGCAGCAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:98944176..98944250 26863196 MeRIP-seq:(Medium) rs577588200 Functional Loss SNV dbSNP153 33..33 33 - - - 105551 RMVar_ID_105551 Human_SNP_ID_408585670 m1A Human chr9 - 98989260 98989260 98989260 GCAAGATCACATGGCACAGCATCCCAGTACTCACCGAGGCTTGAGTGTAGGTGACGGCTTCTAAG GCAAGATCACATGGCACAGCATCCCAGTACTCTCCGAGGCTTGAGTGTAGGTGACGGCTTCTAAG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr9:98989176..98989275 26863196 MeRIP-seq:(Medium) rs1432087176 Functional Loss SNV dbSNP153 33..33 33 - - - 105552 RMVar_ID_105552 Human_SNP_ID_408587735 m1A Human chr9 + 98997051 98997051 98997051 TACCCGAGGGGACCCTGGAAACCACCAACATGAGCATCATCCAGCACAGCAGCCCCAAACAAGGC TACCCGAGGGGACCCTGGAAACCACCAACATGGGCATCATCCAGCACAGCAGCCCCAAACAAGGC A G COL15A1 Ensembl:ENSG00000204291 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:98997026..98997050 26863196 MeRIP-seq:(Medium) rs1564039617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1067201 RMVar_hsa_circ_4753,RMVar_hsa_circ_16416,RMVar_hsa_circ_349083,RMVar_hsa_circ_258213 105553 RMVar_ID_105553 Human_SNP_ID_408614498 m1A Human chr9 + 99105158 99105158 99105158 GTGGGGCGAGGCGAGGTTTGCTGGGGTGAGGCAGCGGCGCGGCCGGGCCGGGCCGGGCCACAGGC GTGGGGCGAGGCGAGGTTTGCTGGGGTGAGGCCGCGGCGCGGCCGGGCCGGGCCGGGCCACAGGC A C TGFBR1 Ensembl:ENSG00000106799 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:99105126..99105350 26863196 MeRIP-seq:(Medium) rs968094003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256530,Human_RBP_ID_798582,Human_RBP_ID_5035771,Human_RBP_ID_5154433,Human_RBP_ID_5329576,Human_RBP_ID_8160027,Human_RBP_ID_9338986,Human_RBP_ID_9441985,Human_RBP_ID_17175211,Human_RBP_ID_18427184,Human_RBP_ID_22466163,Human_RBP_ID_26795873 105554 RMVar_ID_105554 Human_SNP_ID_408614528 m1A Human chr9 - 99105193 99105193 99105193 GCAGCGACCGCCGCCTCCATGGTCCCGCCGCCACCGCCTGTGGCCCGGCCCGGCCCGGCCGCGCC GCAGCGACCGCCGCCTCCATGGTCCCGCCGCCGCCGCCTGTGGCCCGGCCCGGCCCGGCCGCGCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:99105149..99105267 26863196 MeRIP-seq:(Medium) rs886063220 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_677 105555 RMVar_ID_105555 Human_SNP_ID_408614577 m1A Human chr9 - 99105285 99105276 99105285 CGCGCCGCCGCTCACCCGTCGCCCCCGGGAGCAGCGCCGCCGCCGCCGCCGCCGCCGCCGCCAGC CGCGCCGCCGCTCACCCGTCGCCCCCGGGAGC_________GCCGCCGCCGCCGCCGCCGCCAGC CGGCGGCGCT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:99105183..99105325 26863410 MeRIP-seq:(Medium) rs948905780 Functional Loss DEL dbSNP153 33..41 33 - - - 105556 RMVar_ID_105556 Human_SNP_ID_408614687 m1A Human chr9 - 99105555 99105555 99105555 TCCGCCCGACTCCACCTCCCCGGGGAGTCCCGAGCGGGGCGGCCTCGGGCAGCCGGACACGTCCG TCCGCCCGACTCCACCTCCCCGGGGAGTCCCGCGCGGGGCGGCCTCGGGCAGCCGGACACGTCCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:99105546..99105805 26863196 MeRIP-seq:(Medium) rs1183715097 Functional Loss SNV dbSNP153 33..33 33 - - - 105557 RMVar_ID_105557 Human_SNP_ID_408616301 m1A Human chr9 + 99111954 99111954 99111954 GGAGGTAGGACTTGATCTCTCTGCCTTGCAGGAGGATAGGGCTTTGAGTGGATGTGTGGTGGAAA GGAGGTAGGACTTGATCTCTCTGCCTTGCAGGCGGATAGGGCTTTGAGTGGATGTGTGGTGGAAA A C TGFBR1 Ensembl:ENSG00000106799 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:99111950..99112187 26863196 MeRIP-seq:(Medium) rs1287332029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17176523 105558 RMVar_ID_105558 Human_SNP_ID_408620242 m1A Human chr9 + 99128809 99128809 99128809 GTATTATTAGAGTGAATATTGGATAATTTCAAACTGTTAACCTTGAGATTTTTTCTAAGAATCTT GTATTATTAGAGTGAATATTGGATAATTTCAAGCTGTTAACCTTGAGATTTTTTCTAAGAATCTT A G TGFBR1 Ensembl:ENSG00000106799 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:99128807..99129003 26863196 MeRIP-seq:(Medium) rs753385623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2230785,Human_miRNA_ID_2781182,Human_miRNA_ID_2786749 RMVar_hsa_circ_258216,RMVar_hsa_circ_103397 105559 RMVar_ID_105559 Human_SNP_ID_408642537 m1A Human chr9 + 99221797 99221797 99221797 CGCGCGCCTGCAGCGCCAGCGCCGCGTCCAACACCAGCCGCTCAGCGCCGCCCACGCCCAGGTCT CGCGCGCCTGCAGCGCCAGCGCCGCGTCCAACCCCAGCCGCTCAGCGCCGCCCACGCCCAGGTCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr9:99221746..99221915;chr9:99221701..99221828 26863196 MeRIP-seq:(Medium) rs771133469 Functional Loss SNV dbSNP153 33..33 33 - - - 105560 RMVar_ID_105560 Human_SNP_ID_408642847 m1A Human chr9 - 99222326 99222326 99222326 AGATGAGGGTGGCAAGGCGCTGACGCGGACGGATAGAAAGTTACGGAGCCCCCGAAAGACCGGCA AGATGAGGGTGGCAAGGCGCTGACGCGGACGGGTAGAAAGTTACGGAGCCCCCGAAAGACCGGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:99222276..99222516 26863196 MeRIP-seq:(Medium) rs1444773593 Functional Loss SNV dbSNP153 33..33 33 - - - 105561 RMVar_ID_105561 Human_SNP_ID_408643013 m1A Human chr9 + 99222642 99222642 99222642 CCGCCCGGGCGGCGGGATCCACTGTCCGGCAGAGGTAAGGAACCCTGCAGTTCGTTCGCTTCCAG CCGCCCGGGCGGCGGGATCCACTGTCCGGCAGCGGTAAGGAACCCTGCAGTTCGTTCGCTTCCAG A C SEC61B Ensembl:ENSG00000106803 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:99222113..99222719 32194978 MeRIP-seq:(Medium) rs1198669365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707506,Human_RBP_ID_966141,Human_RBP_ID_9230773,Human_RBP_ID_19143584,Human_RBP_ID_22466428 Human_Splice_Rec_1067466,Human_Splice_Rec_1067467,Human_Splice_Rec_1067472,Human_Splice_Rec_1067473,Human_Splice_Rec_1067478 RMVar_hsa_circ_92312,RMVar_hsa_circ_96960,RMVar_hsa_circ_258226,RMVar_hsa_circ_258227 105562 RMVar_ID_105562 Human_SNP_ID_408778747 m1A Human chr9 - 99819859 99819859 99819859 CCATCTTGGACTCGGTTCGACCAGGTCTGGTGACCGGCGACGAGGGGCCGGGCTCGGCGCCGGGG CCATCTTGGACTCGGTTCGACCAGGTCTGGTGGCCGGCGACGAGGGGCCGGGCTCGGCGCCGGGG T C AL359710.1,STX17-AS1 Ensembl:ENSG00000237461,Ensembl:ENSG00000255145 lincRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:99819560..99819905 26863196 MeRIP-seq:(Medium) rs1319332142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1067531,Human_Splice_Rec_1067541 105563 RMVar_ID_105563 Human_SNP_ID_408779489 m1A Human chr9 + 99822177 99822177 99822177 GCAGTGGCCGTGGAGGTGGGAACAGCGGCGGCATCCTCCCCCCTGGTCACAGCCCAAGCCAGGAC GCAGTGGCCGTGGAGGTGGGAACAGCGGCGGCCTCCTCCCCCCTGGTCACAGCCCAAGCCAGGAC A C NR4A3 Ensembl:ENSG00000119508 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:99822126..99822200 26863196 MeRIP-seq:(Medium) rs941380783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258235,RMVar_hsa_circ_80544 105564 RMVar_ID_105564 Human_SNP_ID_408780388 m1A Human chr9 + 99825777 99825777 99825777 CCTCGCCGGACGTCCGCTCCTCCTACACTCTCAGCCTCCGCTGGAGAGACCCCCAGCCCCACCAT CCTCGCCGGACGTCCGCTCCTCCTACACTCTCTGCCTCCGCTGGAGAGACCCCCAGCCCCACCAT A T NR4A3 Ensembl:ENSG00000119508 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:99825728..99828084 26863196 MeRIP-seq:(Medium) rs961042834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1067583,Human_Splice_Rec_1067591,Human_Splice_Rec_1067607 RMVar_hsa_circ_258235,RMVar_hsa_circ_80544,RMVar_hsa_circ_123792,RMVar_hsa_circ_258236 105565 RMVar_ID_105565 Human_SNP_ID_408780940 m1A Human chr9 + 99828067 99828067 99828067 CTGCAGATATGCCCTGCGTCCAAGCCCAATATAGCCCTTCCCCTCCAGGTTCCAGTTATGCGGCG CTGCAGATATGCCCTGCGTCCAAGCCCAATATGGCCCTTCCCCTCCAGGTTCCAGTTATGCGGCG A G NR4A3 Ensembl:ENSG00000119508 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:99825702..99828190 26863196 MeRIP-seq:(Medium) rs745430984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1067584,Human_Splice_Rec_1067594,Human_Splice_Rec_1067608,Human_Splice_Rec_1067620 RMVar_hsa_circ_101466,RMVar_hsa_circ_258235,RMVar_hsa_circ_80544,RMVar_hsa_circ_123792,RMVar_hsa_circ_258236,RMVar_hsa_circ_105136,RMVar_hsa_circ_258237,RMVar_hsa_circ_258238 105566 RMVar_ID_105566 Human_SNP_ID_408798093 m1A Human chr9 + 99906705 99906705 99906705 GCCCACCGACCGGCCTCGAGCGCCCCGGCGGGAGGTAAGGGGCTCTCTGGAGGCCGCCTTTGGGG GCCCACCGACCGGCCTCGAGCGCCCCGGCGGGCGGTAAGGGGCTCTCTGGAGGCCGCCTTTGGGG A C STX17 Ensembl:ENSG00000136874 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:99906694..99906772;chr9:99906694..99906910 26863196 MeRIP-seq:(Medium) rs1191341616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036284,Human_RBP_ID_18427185 Human_Splice_Rec_1067631,Human_Splice_Rec_1067645,Human_Splice_Rec_1067659,Human_Splice_Rec_1067663,Human_Splice_Rec_1067671,Human_Splice_Rec_1067681 105567 RMVar_ID_105567 Human_SNP_ID_408841148 m1A Human chr9 - 100098874 100098874 100098874 ACCCAACCCAACCTAGCCCAGTCCCAGCCGCCAGCGCCTGTCCCTGTCACGGACCCCAGCGTTAC ACCCAACCCAACCTAGCCCAGTCCCAGCCGCCGGCGCCTGTCCCTGTCACGGACCCCAGCGTTAC T C ERP44 Ensembl:ENSG00000023318 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:100098826..100099000 26863196 MeRIP-seq:(Medium) rs769910669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035780,Human_RBP_ID_18962929,Human_RBP_ID_27128375 Human_Splice_Rec_1067741 105568 RMVar_ID_105568 Human_SNP_ID_408841179 m1A Human chr9 + 100098947 100098947 100098947 GGCTGGGCTCCGGGAGCCGACGGCAGCGGAGGATTCTCCAGGCAGCGGCACCTCGTCCTCTCGAC GGCTGGGCTCCGGGAGCCGACGGCAGCGGAGGTTTCTCCAGGCAGCGGCACCTCGTCCTCTCGAC A T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:100098866..100098981 26863410 MeRIP-seq:(Medium) rs562581238 Functional Loss SNV dbSNP153 33..33 33 - - - 105569 RMVar_ID_105569 Human_SNP_ID_408851305 m1A Human chr9 + 100140716 100140716 100140716 TGGGCGATGTTTCTTAGGGCTGCTTCGAGCGGAATTAGGGGCGGTGTGGGAACCTAGAATGGGAG TGGGCGATGTTTCTTAGGGCTGCTTCGAGCGGGATTAGGGGCGGTGTGGGAACCTAGAATGGGAG A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:100140665..100140840 26863196 MeRIP-seq:(Medium) rs1421610905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7882018,Human_RBP_ID_24276234 RMVar_hsa_circ_50475,RMVar_hsa_circ_333575,RMVar_hsa_circ_366034,RMVar_hsa_circ_31388,RMVar_hsa_circ_37468,RMVar_hsa_circ_18273,RMVar_hsa_circ_60561 105570 RMVar_ID_105570 Human_SNP_ID_408852009 m1A Human chr9 - 100143774 100143774 100143774 TTCCCTTGCCTCCATAACTGTTGCAGGTACTGACGGCCAGGCTTCTAAACCTCTTAAAACTCCCC TTCCCTTGCCTCCATAACTGTTGCAGGTACTGCCGGCCAGGCTTCTAAACCTCTTAAAACTCCCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:100143752..100143819 26863196 MeRIP-seq:(Medium) rs1259394330 Functional Loss SNV dbSNP153 33..33 33 - - - 105571 RMVar_ID_105571 Human_SNP_ID_408852659 m1A Human chr9 + 100146283 100146283 100146283 GATTTGGGTAGGTAAAGGAAAATTACAGTCAAAGGGGGGTTGTTCTCTGGCAGGAGTGGGGGTCA GATTTGGGTAGGTAAAGGAAAATTACAGTCAAGGGGGGGTTGTTCTCTGGCAGGAGTGGGGGTCA A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:100146234..100146320 26863196 MeRIP-seq:(Medium) rs1024020048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24276238 RMVar_hsa_circ_50475,RMVar_hsa_circ_333575,RMVar_hsa_circ_366034,RMVar_hsa_circ_31388,RMVar_hsa_circ_37468,RMVar_hsa_circ_18273,RMVar_hsa_circ_60561 105572 RMVar_ID_105572 Human_SNP_ID_408855631 m1A Human chr9 + 100159273 100159271 100159274 ATTCAATGAGAAGTTTTAGGGAAGGTTTCATGAAGGAGAGAGAATTTGAACTAGATATTGAAAAA ATTCAATGAGAAGTTTTAGGGAAGGTTTCAT___GGAGAGAGAATTTGAACTAGATATTGAAAAA TGAA T INVS Ensembl:ENSG00000119509 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:100159146..100159275 26863196 MeRIP-seq:(Medium) rs1282585112 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_16524969 RMVar_hsa_circ_50475,RMVar_hsa_circ_333575,RMVar_hsa_circ_366034,RMVar_hsa_circ_31388,RMVar_hsa_circ_37468,RMVar_hsa_circ_18273,RMVar_hsa_circ_60561 105573 RMVar_ID_105573 Human_SNP_ID_408900679 m1A Human chr9 + 100352823 100352823 100352823 CGGGGCGAGAAGCCCGAGAAGACAAGCGAGGGAGCAGAAGCCCACGGGGCAACAGCGTGCGCCGC CGGGGCGAGAAGCCCGAGAAGACAAGCGAGGGGGCAGAAGCCCACGGGGCAACAGCGTGCGCCGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:100352751..100352825 32194978 MeRIP-seq:(Medium) rs1244665106 Functional Loss SNV dbSNP153 33..33 33 - - - 105574 RMVar_ID_105574 Human_SNP_ID_408918755 m1A Human chr9 - 100427389 100427372 100427389 CGGCCCGCCCGGAAGGGGAGCCTCCTACCTGCAGCGGCGGCGCGGCAGCCGCGGCGACCGGGGGA CGGCCCGCCCGGAAGGGGAGCCTCCTACCTGC_________________CGCGGCGACCGGGGGA GGCTGCCGCGCCGCCGCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr9:100427299..100427583;chr9:100427303..100427437 26863196,32194978 MeRIP-seq:(Medium) rs1209779794 Functional Loss DEL dbSNP153 33..49 33 - - - 105575 RMVar_ID_105575 Human_SNP_ID_408922365 m1A Human chr9 + 100442308 100442305 100442309 GCATGCTGCCGGAGCAGCTCTACTTCCTGCAGAGCCCCCCGGAGGAGGAGCCCGAATACCACCCC GCATGCTGCCGGAGCAGCTCTACTTCCTGC____CCCCCCGGAGGAGGAGCCCGAATACCACCCC CAGAG C MSANTD3,MSANTD3-TMEFF1 Ensembl:ENSG00000066697,Ensembl:ENSG00000251349 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:100442159..100442375;chr9:100442146..100442313 26863196 MeRIP-seq:(Medium) rs1328673839 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_90157,Human_RBP_ID_23094734,Human_RBP_ID_27832554 Human_Splice_Rec_1067937,Human_Splice_Rec_1067945,Human_Splice_Rec_1067951,Human_Splice_Rec_1067955,Human_Splice_Rec_1067959,Human_Splice_Rec_1067961,Human_Splice_Rec_1067965 RMVar_hsa_circ_258302,RMVar_hsa_circ_37664,RMVar_hsa_circ_280615,RMVar_hsa_circ_258303,RMVar_hsa_circ_258301 105576 RMVar_ID_105576 Human_SNP_ID_408929408 m1A Human chr9 + 100473971 100473971 100473971 GGGTGCGTCCGAGTGTGTCGAGTGGCTGGGCGAGGGCGGCCCGGCGTGTGGGGAGGCGGTGGGGC GGGTGCGTCCGAGTGTGTCGAGTGGCTGGGCGTGGGCGGCCCGGCGTGTGGGGAGGCGGTGGGGC A T TMEFF1,MSANTD3-TMEFF1 Ensembl:ENSG00000241697,Ensembl:ENSG00000251349 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:100473921..100474071 26863196 MeRIP-seq:(Medium) rs913947790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258305,RMVar_hsa_circ_258304 105577 RMVar_ID_105577 Human_SNP_ID_408929522 m1A Human chr9 + 100474314 100474314 100474314 CGGGTTGTCTTGAGGACGCGGTTTGGCGATGCAGAGTGACTGTGTGTGTGCGCGCGCGCGCGCGT CGGGTTGTCTTGAGGACGCGGTTTGGCGATGCCGAGTGACTGTGTGTGTGCGCGCGCGCGCGCGT A C TMEFF1,MSANTD3-TMEFF1 Ensembl:ENSG00000241697,Ensembl:ENSG00000251349 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:100474297..100474379 26863196 MeRIP-seq:(Medium) rs909434197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24276546 RMVar_hsa_circ_258305,RMVar_hsa_circ_258304 105578 RMVar_ID_105578 Human_SNP_ID_408954301 m1A Human chr9 - 100576804 100576804 100576804 GTCTTAGAATTACCATGTGGTACAAATTTGTGAAAGCAATTTCTGTATTTAAAAACATAAAACAA GTCTTAGAATTACCATGTGGTACAAATTTGTGGAAGCAATTTCTGTATTTAAAAACATAAAACAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:100576756..100576839 32194978 MeRIP-seq:(Medium) rs1003365668 Functional Loss SNV dbSNP153 33..33 33 - - - 105579 RMVar_ID_105579 Human_SNP_ID_409153199 m1A Human chr9 + 101398540 101398540 101398540 GAGACCAAAATTCTCTACATGGTGTCCCTGAGACTGTCCACATGAAGACTCTTCTGGTAATGCCC GAGACCAAAATTCTCTACATGGTGTCCCTGAGCCTGTCCACATGAAGACTCTTCTGGTAATGCCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:101390615..101398614 32194978 MeRIP-seq:(Medium) rs769460074 Functional Loss SNV dbSNP153 33..33 33 - - - 105580 RMVar_ID_105580 Human_SNP_ID_409153212 m1A Human chr9 - 101398560 101398560 101398560 ATGGCGGCGCGATCTGTGTCGGGCATTACCAGAAGAGTCTTCATGTGGACAGTCTCAGGGACACC ATGGCGGCGCGATCTGTGTCGGGCATTACCAGGAGAGTCTTCATGTGGACAGTCTCAGGGACACC T C MRPL50 Ensembl:ENSG00000136897 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:101398466..101398600 26863196 MeRIP-seq:(Medium) rs776748137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707858,Human_RBP_ID_797459,Human_RBP_ID_847247,Human_RBP_ID_1700640,Human_RBP_ID_2058856,Human_RBP_ID_5036292,Human_RBP_ID_9407114,Human_RBP_ID_16528030,Human_RBP_ID_18427188,Human_RBP_ID_26360396 Human_Splice_Rec_1068057 RMVar_hsa_circ_101206,RMVar_hsa_circ_258334 105581 RMVar_ID_105581 Human_SNP_ID_409153391 m1A Human chr9 + 101398907 101398907 101398907 GGAGGAGGAACTGGCAGCGGGGAGGAGGCTCTAGCGAGGCCTGAAAGGCTGCGTAACCAGGCAGG GGAGGAGGAACTGGCAGCGGGGAGGAGGCTCTGGCGAGGCCTGAAAGGCTGCGTAACCAGGCAGG A G ZNF189 Ensembl:ENSG00000136870 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:101398865..101399122 26863196 MeRIP-seq:(Medium) rs1019510759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5004246,Human_RBP_ID_18427189 105582 RMVar_ID_105582 Human_SNP_ID_409155037 m1A Human chr9 + 101405316 101405316 101405316 TGTTGGCAGCCTAAAGACTGGAGCCAAAGATTATAAGGCAGCTACATGATTGTGAGGGATGAAAG TGTTGGCAGCCTAAAGACTGGAGCCAAAGATTGTAAGGCAGCTACATGATTGTGAGGGATGAAAG A G ZNF189 Ensembl:ENSG00000136870 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:101405313..101405746 26863196 MeRIP-seq:(Medium) rs1257536404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111607,RMVar_hsa_circ_258336 105583 RMVar_ID_105583 Human_SNP_ID_409172845 m1A Human chr9 - 101475653 101475653 101475653 ACAGGTCCGGACCTCTCCCTCCACACAGCCACACTGCCTCATGCAGTCTGACCCACCCAGTGAGG ACAGGTCCGGACCTCTCCCTCCACACAGCCACGCTGCCTCATGCAGTCTGACCCACCCAGTGAGG T C PGAP4 Ensembl:ENSG00000165152 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:101475556..101475756 32194978 MeRIP-seq:(Medium) rs1044452461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707910,Human_RBP_ID_1337248,Human_RBP_ID_27368823 Human_miRNA_ID_694928,Human_miRNA_ID_1014305,Human_miRNA_ID_1018470,Human_miRNA_ID_1022451,Human_miRNA_ID_1296314,Human_miRNA_ID_1300242,Human_miRNA_ID_1304969 105584 RMVar_ID_105584 Human_SNP_ID_409172901 m1A Human chr9 - 101475903 101475903 101475903 ACACATCGGGCTCTTCTCCAGTCTCCGGTACAACTTTCATCCCAGTCTCCTCTAGGGTGCCAAGA ACACATCGGGCTCTTCTCCAGTCTCCGGTACAGCTTTCATCCCAGTCTCCTCTAGGGTGCCAAGA T C PGAP4 Ensembl:ENSG00000165152 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:101475854..101475954 32194978 MeRIP-seq:(Medium) rs1314234273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17320594,Human_RBP_ID_17434899 Human_miRNA_ID_848280,Human_miRNA_ID_1386990 105585 RMVar_ID_105585 Human_SNP_ID_409172980 m1A Human chr9 + 101476103 101476103 101476103 GCCGGGAAGAGCATGGCTGGGGTGCAACACTGAGAGGCAGGAACCACACTGTACAGGGAAGGACT GCCGGGAAGAGCATGGCTGGGGTGCAACACTGTGAGGCAGGAACCACACTGTACAGGGAAGGACT A T TMEM246-AS1 Ensembl:ENSG00000225376 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:101476053..101476153 32194978 MeRIP-seq:(Medium) rs755710873 Functional Loss SNV dbSNP153 33..33 33 - - - 105586 RMVar_ID_105586 Human_SNP_ID_409192474 m1A Human chr9 + 101552589 101552589 101552589 CGAGAACGAGAAAGGAGGGAGAAGGAGAGGGAACGAGAAAGAGAACGGGAGAAGGAGAAGGAGAG CGAGAACGAGAAAGGAGGGAGAAGGAGAGGGAGCGAGAAAGAGAACGGGAGAAGGAGAAGGAGAG A G RNF20 Ensembl:ENSG00000155827 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr9:101552541..101552708;chr9:101552540..101552725 26863196 MeRIP-seq:(Medium) rs1035437795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256171,Human_RBP_ID_268573,Human_RBP_ID_26195814,Human_RBP_ID_26361932 RMVar_hsa_circ_94084,RMVar_hsa_circ_258344,RMVar_hsa_circ_22653,RMVar_hsa_circ_58440,RMVar_hsa_circ_85291,RMVar_hsa_circ_258345 105587 RMVar_ID_105587 Human_SNP_ID_409854102 m1A Human chr9 + 104094369 104094369 104094369 TTGAGAGCGGTGTGGCAGGTGTTGTAGCCGCTATGGTGAAGTTCGCTTTGTAGCGGCCCCGGCTA TTGAGAGCGGTGTGGCAGGTGTTGTAGCCGCTGTGGTGAAGTTCGCTTTGTAGCGGCCCCGGCTA A G SMC2 Ensembl:ENSG00000136824 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:104094318..104094475 26863196 MeRIP-seq:(Medium) rs1010949406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5004476,Human_RBP_ID_24277004 Human_Splice_Rec_1068415 RMVar_hsa_circ_105450,RMVar_hsa_circ_258354 105588 RMVar_ID_105588 Human_SNP_ID_409854215 m1A Human chr9 - 104094601 104094601 104094601 AGAAGCTAGCCTTTATTTCTAAGGATCACCTAAGGTCCCTCTGCCACTGGTCCCCCTCCCTACAG AGAAGCTAGCCTTTATTTCTAAGGATCACCTACGGTCCCTCTGCCACTGGTCCCCCTCCCTACAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:104094592..104094723 26863196 MeRIP-seq:(Medium) rs946415061 Functional Loss SNV dbSNP153 33..33 33 - - - 105589 RMVar_ID_105589 Human_SNP_ID_409854219 m1A Human chr9 - 104094606 104094606 104094606 CGAACAGAAGCTAGCCTTTATTTCTAAGGATCACCTAAGGTCCCTCTGCCACTGGTCCCCCTCCC CGAACAGAAGCTAGCCTTTATTTCTAAGGATCGCCTAAGGTCCCTCTGCCACTGGTCCCCCTCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:104094588..104094678 26863196 MeRIP-seq:(Medium) rs1408713270 Functional Loss SNV dbSNP153 33..33 33 - - - 105590 RMVar_ID_105590 Human_SNP_ID_529060986 m1A Human chr13 + 45030645 45030645 45030645 ACCTCAGGTGATCTACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATCAGCCACCATGC ACCTCAGGTGATCTACCTGCCTCGGCCTCCCAGAATGCTGGGATTACAGGCATCAGCCACCATGC A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1280581942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26425537 RMVar_hsa_circ_163159 105591 RMVar_ID_105591 Human_SNP_ID_529091027 m1A Human chr13 - 45157097 45157097 45157097 GGCTACCCCTTTTGCCTCCTTCAAGACTGTTCAAATTTCACCTTCTCAATGAGGTCCCACCCCCA GGCTACCCCTTTTGCCTCCTTCAAGACTGTTCGAATTTCACCTTCTCAATGAGGTCCCACCCCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45157094..45157285 26863196 MeRIP-seq:(Medium) rs1319100997 Functional Loss SNV dbSNP153 33..33 33 - - - 105592 RMVar_ID_105592 Human_SNP_ID_529135698 m1A Human chr13 - 45334531 45334531 45334531 ATACAAGTATTTTGGTCTGAGCGTTTGGAAGAAAGTTGGCACTGAGGTGGGAAGTCGAGTTTAGT ATACAAGTATTTTGGTCTGAGCGTTTGGAAGACAGTTGGCACTGAGGTGGGAAGTCGAGTTTAGT T G TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:45334416..45334596 26863196 MeRIP-seq:(Medium) rs971250919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1083781,Human_RBP_ID_6286120,Human_RBP_ID_12166343,Human_RBP_ID_23596991 105593 RMVar_ID_105593 Human_SNP_ID_529137622 m1A Human chr13 + 45340104 45340104 45340104 ATATCGACACCAGTGATTACTGTGCTTTCGGTACCTTCGCCCTCGGGGCCTTCAGCGGAGGCATT ATATCGACACCAGTGATTACTGTGCTTTCGGTCCCTTCGCCCTCGGGGCCTTCAGCGGAGGCATT A C AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45340055..45340211 26863196 MeRIP-seq:(Medium) rs1390222193 Functional Loss SNV dbSNP153 33..33 33 - - - 105594 RMVar_ID_105594 Human_SNP_ID_529137655 m1A Human chr13 + 45340176 45340173 45340176 ATGAGCGAGTCATCAATGTTACCTTCTGTCCTACTGACCATCTGCATTAAGAAAAAGCAGTATAA ATGAGCGAGTCATCAATGTTACCTTCTGTC___CTGACCATCTGCATTAAGAAAAAGCAGTATAA CCTA C AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:45340126..45340200 32194978 MeRIP-seq:(Medium) rs768455024 Functional Loss DEL dbSNP153 31..33 33 - - - 105595 RMVar_ID_105595 Human_SNP_ID_529137656 m1A Human chr13 + 45340176 45340176 45340176 ATGAGCGAGTCATCAATGTTACCTTCTGTCCTACTGACCATCTGCATTAAGAAAAAGCAGTATAA ATGAGCGAGTCATCAATGTTACCTTCTGTCCTCCTGACCATCTGCATTAAGAAAAAGCAGTATAA A C AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:45340126..45340200 32194978 MeRIP-seq:(Medium) rs563164026 Functional Loss SNV dbSNP153 33..33 33 - - - 105596 RMVar_ID_105596 Human_SNP_ID_529137658 m1A Human chr13 + 45340183 45340183 45340183 AGTCATCAATGTTACCTTCTGTCCTACTGACCATCTGCATTAAGAAAAAGCAGTATAATTGCAAA AGTCATCAATGTTACCTTCTGTCCTACTGACCTTCTGCATTAAGAAAAAGCAGTATAATTGCAAA A T AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:45339952..45340235 26863196 MeRIP-seq:(Medium) rs778014296 Functional Loss SNV dbSNP153 33..33 33 - - - 105597 RMVar_ID_105597 Human_SNP_ID_529138000 m1A Human chr13 + 45340681 45340681 45340681 GAGCGGAGGAAACCCGAGCCCGCTCGGCCCGGACTCCCCCACGCGCAGGCCCGACCGACTCACCT GAGCGGAGGAAACCCGAGCCCGCTCGGCCCGGCCTCCCCCACGCGCAGGCCCGACCGACTCACCT A C AL138963.4 Ensembl:ENSG00000273149 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr13:45340667..45340823 26863410 MeRIP-seq:(Medium) rs754286179 Functional Loss SNV dbSNP153 33..33 33 - - - 105598 RMVar_ID_105598 Human_SNP_ID_529138001 m1A Human chr13 + 45340681 45340681 45340681 GAGCGGAGGAAACCCGAGCCCGCTCGGCCCGGACTCCCCCACGCGCAGGCCCGACCGACTCACCT GAGCGGAGGAAACCCGAGCCCGCTCGGCCCGGTCTCCCCCACGCGCAGGCCCGACCGACTCACCT A T AL138963.4 Ensembl:ENSG00000273149 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr13:45340667..45340823 26863410 MeRIP-seq:(Medium) rs754286179 Functional Loss SNV dbSNP153 33..33 33 - - - 105599 RMVar_ID_105599 Human_SNP_ID_529138232 m1A Human chr13 - 45341079 45341079 45341079 GTGCTAAGCTAGCGCCGTCGTCGTCTCCCTTCAGTCGCCATCATGATTATCTACCGGGACCTCAT GTGCTAAGCTAGCGCCGTCGTCGTCTCCCTTCGGTCGCCATCATGATTATCTACCGGGACCTCAT T C TPT1 Ensembl:ENSG00000133112 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:45340634..45341200 26863196 MeRIP-seq:(Medium) rs370176126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_436571,Human_RBP_ID_880137,Human_RBP_ID_996586,Human_RBP_ID_1484544,Human_RBP_ID_1809634,Human_RBP_ID_3430648,Human_RBP_ID_4270846,Human_RBP_ID_5417714,Human_RBP_ID_5438524,Human_RBP_ID_5462793,Human_RBP_ID_5492746,Human_RBP_ID_6286202,Human_RBP_ID_8392607,Human_RBP_ID_8790320,Human_RBP_ID_9280830,Human_RBP_ID_12166579,Human_RBP_ID_18189316,Human_RBP_ID_18206791,Human_RBP_ID_18435263,Human_RBP_ID_18640839,Human_RBP_ID_22796212,Human_RBP_ID_23126299,Human_RBP_ID_26425578,Human_RBP_ID_26807467,Human_RBP_ID_26916339,Human_RBP_ID_27221682,Human_RBP_ID_27428014 Human_Splice_Rec_1461195,Human_Splice_Rec_1461205,Human_Splice_Rec_1461215,Human_Splice_Rec_1461245,Human_Splice_Rec_1461253,Human_Splice_Rec_1461271,Human_Splice_Rec_1461279,Human_Splice_Rec_1461287 Human_miRNA_ID_2617820 RMVar_hsa_circ_121231,RMVar_hsa_circ_163175,RMVar_hsa_circ_60043 105600 RMVar_ID_105600 Human_SNP_ID_529138252 m1A Human chr13 + 45341102 45341102 45341102 GATGGCGACTGAAGGGAGACGACGACGGCGCTAGCTTAGCACGAGCCTGAAACTCGGAGCGAGCG GATGGCGACTGAAGGGAGACGACGACGGCGCTGGCTTAGCACGAGCCTGAAACTCGGAGCGAGCG A G AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr13:45341051..45341200 26863410 MeRIP-seq:(Medium) rs752572384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5417713 Human_Splice_Rec_1461290 105601 RMVar_ID_105601 Human_SNP_ID_529138263 m1A Human chr13 - 45341117 45341117 45341117 GCTCCGGCTGCACCGCGCTCGCTCCGAGTTTCAGGCTCGTGCTAAGCTAGCGCCGTCGTCGTCTC GCTCCGGCTGCACCGCGCTCGCTCCGAGTTTCCGGCTCGTGCTAAGCTAGCGCCGTCGTCGTCTC T G TPT1 Ensembl:ENSG00000133112 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr13:45341058..45341183 26863410 MeRIP-seq:(Medium) rs1215121788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_436571,Human_RBP_ID_1169958,Human_RBP_ID_1484546,Human_RBP_ID_3430648,Human_RBP_ID_4270846,Human_RBP_ID_5417714,Human_RBP_ID_5462793,Human_RBP_ID_5492746,Human_RBP_ID_8392607,Human_RBP_ID_18189317,Human_RBP_ID_18640843,Human_RBP_ID_22494666,Human_RBP_ID_23126300,Human_RBP_ID_26807469,Human_RBP_ID_27428018 Human_Splice_Rec_1461195,Human_Splice_Rec_1461205,Human_Splice_Rec_1461215,Human_Splice_Rec_1461245,Human_Splice_Rec_1461253,Human_Splice_Rec_1461271,Human_Splice_Rec_1461279,Human_Splice_Rec_1461287 Human_miRNA_ID_2895521 RMVar_hsa_circ_121231,RMVar_hsa_circ_163175,RMVar_hsa_circ_60043 105602 RMVar_ID_105602 Human_SNP_ID_529138267 m1A Human chr13 + 45341127 45341127 45341127 CGGCGCTAGCTTAGCACGAGCCTGAAACTCGGAGCGAGCGCGGTGCAGCCGGAGCGGCGCTCGGG CGGCGCTAGCTTAGCACGAGCCTGAAACTCGGCGCGAGCGCGGTGCAGCCGGAGCGGCGCTCGGG A C AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45340668..45341221 26863196 MeRIP-seq:(Medium) rs867355393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461290 105603 RMVar_ID_105603 Human_SNP_ID_529138268 m1A Human chr13 + 45341127 45341127 45341127 CGGCGCTAGCTTAGCACGAGCCTGAAACTCGGAGCGAGCGCGGTGCAGCCGGAGCGGCGCTCGGG CGGCGCTAGCTTAGCACGAGCCTGAAACTCGGGGCGAGCGCGGTGCAGCCGGAGCGGCGCTCGGG A G AL138963.4 Ensembl:ENSG00000273149 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45340668..45341221 26863196 MeRIP-seq:(Medium) rs867355393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461290 105604 RMVar_ID_105604 Human_SNP_ID_529138297 m1A Human chr13 - 45341155 45341155 45341155 CGGCCTTTTCCGCCCGCTCCCCCCTCCCCCCGAGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGA CGGCCTTTTCCGCCCGCTCCCCCCTCCCCCCGGGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGA T C TPT1 Ensembl:ENSG00000133112 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:45341059..45341186 26863410 MeRIP-seq:(Medium) rs543602973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230620,Human_RBP_ID_436572,Human_RBP_ID_756369,Human_RBP_ID_4270846,Human_RBP_ID_5417717,Human_RBP_ID_5438526,Human_RBP_ID_5462793,Human_RBP_ID_5492746,Human_RBP_ID_6286205,Human_RBP_ID_8248890,Human_RBP_ID_9032131,Human_RBP_ID_22532543,Human_RBP_ID_23126301,Human_RBP_ID_26916340 RMVar_hsa_circ_121231,RMVar_hsa_circ_163175,RMVar_hsa_circ_60043 105605 RMVar_ID_105605 Human_SNP_ID_529138298 m1A Human chr13 - 45341155 45341155 45341155 CGGCCTTTTCCGCCCGCTCCCCCCTCCCCCCGAGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGA CGGCCTTTTCCGCCCGCTCCCCCCTCCCCCCGCGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGA T G TPT1 Ensembl:ENSG00000133112 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:45341059..45341186 26863410 MeRIP-seq:(Medium) rs543602973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230620,Human_RBP_ID_436572,Human_RBP_ID_756369,Human_RBP_ID_4270846,Human_RBP_ID_5417717,Human_RBP_ID_5438526,Human_RBP_ID_5462793,Human_RBP_ID_5492746,Human_RBP_ID_6286205,Human_RBP_ID_8248890,Human_RBP_ID_9032131,Human_RBP_ID_22532543,Human_RBP_ID_23126301,Human_RBP_ID_26916340 RMVar_hsa_circ_121231,RMVar_hsa_circ_163175,RMVar_hsa_circ_60043 105606 RMVar_ID_105606 Human_SNP_ID_529147648 m1A Human chr13 + 45372298 45372298 45372298 GGAGGGAACGCCATGAAAGAGAGGCCAGTAGCATGTGCGGGGCAGAGAGGGAGCCGGCTTCTTAG GGAGGGAACGCCATGAAAGAGAGGCCAGTAGCGTGTGCGGGGCAGAGAGGGAGCCGGCTTCTTAG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45372248..45372352 26863196 MeRIP-seq:(Medium) rs1438569034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 105607 RMVar_ID_105607 Human_SNP_ID_529147675 m1A Human chr13 + 45372389 45372387 45372389 AAGCCAGCACCAACGGGAAGGGCTGCATCTGGAGAGAGAGGGAGAGCAGCTGCAGGTTGGTCAAG AAGCCAGCACCAACGGGAAGGGCTGCATCTG__GAGAGAGGGAGAGCAGCTGCAGGTTGGTCAAG GGA G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:45372269..45372392 26863196 MeRIP-seq:(Medium) rs1376992477 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3440474 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 105608 RMVar_ID_105608 Human_SNP_ID_529176405 m1A Human chr13 - 45465008 45465005 45465008 CCATCGCCGCCGCCCTCGCGGCCTTCAGCAGCAGCGAGATGGAGGGGACCCCGACAGAGAGACCT CCATCGCCGCCGCCCTCGCGGCCTTCAGCAGC___GAGATGGAGGGGACCCCGACAGAGAGACCT CGCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45464959..45465225 26863196 MeRIP-seq:(Medium) rs1566235568 Functional Loss DEL dbSNP153 33..35 33 - - - 105609 RMVar_ID_105609 Human_SNP_ID_529176409 m1A Human chr13 - 45465014 45465014 45465014 CCTCCGCCATCGCCGCCGCCCTCGCGGCCTTCAGCAGCAGCGAGATGGAGGGGACCCCGACAGAG CCTCCGCCATCGCCGCCGCCCTCGCGGCCTTCGGCAGCAGCGAGATGGAGGGGACCCCGACAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr13:45464951..45465175;chr13:45464963..45465196 26863196 MeRIP-seq:(Medium) rs1235280302 Functional Loss SNV dbSNP153 33..33 33 - - - 105610 RMVar_ID_105610 Human_SNP_ID_529176456 m1A Human chr13 + 45465125 45465125 45465125 GGAAAAGCTGGCTCTCTGGGATCGGAGACCGGACACGACGGCGCCGCTGACCGACAGGCAGACGG GGAAAAGCTGGCTCTCTGGGATCGGAGACCGGGCACGACGGCGCCGCTGACCGACAGGCAGACGG A G COG3 Ensembl:ENSG00000136152 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:45464976..45465200;chr13:45464962..45465133 26863196 MeRIP-seq:(Medium) rs1307662926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1462039,Human_Splice_Rec_1462041,Human_Splice_Rec_1462085,Human_Splice_Rec_1462107 RMVar_hsa_circ_163201,RMVar_hsa_circ_102914 105611 RMVar_ID_105611 Human_SNP_ID_529176777 m1A Human chr13 + 45466478 45466478 45466478 CTTCACATTCACTGTTGTATGCTCAGCCATCAAATAGGCGTTCTTTCTTGGGTTTCTTTTTCCAC CTTCACATTCACTGTTGTATGCTCAGCCATCAGATAGGCGTTCTTTCTTGGGTTTCTTTTTCCAC A G COG3 Ensembl:ENSG00000136152 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45466473..45466569 26863196 MeRIP-seq:(Medium) rs1285231173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3430675 RMVar_hsa_circ_163201,RMVar_hsa_circ_102914 105612 RMVar_ID_105612 Human_SNP_ID_529297946 m1A Human chr13 - 45967793 45967787 45967793 AACAGGGATCGAGATAGATTGCGAGAACGAGAACGAGAGAGAGAACGAGACAAAAGGAGAGACTT AACAGGGATCGAGATAGATTGCGAGAACGAGA______GAGAGAACGAGACAAAAGGAGAGACTT CTCTCGT C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45967644..45968018 26863196 MeRIP-seq:(Medium) rs768609441 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_12168010,Human_RBP_ID_18640914,Human_RBP_ID_23597333,Human_RBP_ID_24543554,Human_RBP_ID_24551432,Human_RBP_ID_26324337,Human_RBP_ID_27807926 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_364506,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037 105613 RMVar_ID_105613 Human_SNP_ID_529298310 m1A Human chr13 - 45969087 45969087 45969087 CCCCCACCAATACCACCAATAATACTTTTGCCAATGAAGACTCACACAGAAAATGCCACAGAACA CCCCCACCAATACCACCAATAATACTTTTGCCGATGAAGACTCACACAGAAAATGCCACAGAACA T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:45969039..45969145 26863196 MeRIP-seq:(Medium) rs376194256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37715,Human_RBP_ID_4271040,Human_RBP_ID_17246095,Human_RBP_ID_18640917 Human_miRNA_ID_2132517,Human_miRNA_ID_2947610 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 105614 RMVar_ID_105614 Human_SNP_ID_529298333 m1A Human chr13 - 45969135 45969135 45969135 CCGCCACCTCTTTCAGCACATCTGCCATCACTATTTCCACCTCTGCCACCCCCACCAATACCACC CCGCCACCTCTTTCAGCACATCTGCCATCACTGTTTCCACCTCTGCCACCCCCACCAATACCACC T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45969084..45969199 26863196 MeRIP-seq:(Medium) rs144601974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8790390,Human_RBP_ID_9032185,Human_RBP_ID_9280845,Human_RBP_ID_9367489,Human_RBP_ID_17244948,Human_RBP_ID_17359895,Human_RBP_ID_17476792,Human_RBP_ID_18640918,Human_RBP_ID_27429191 Human_miRNA_ID_2273162 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 105615 RMVar_ID_105615 Human_SNP_ID_529298377 m1A Human chr13 + 45969235 45969235 45969235 GTTGTAGCAGTGGCAGTAGCCACAGGCGGTGGAGGAGGAAGAAGAGAAGATAGAGGAGAAGGGGT GTTGTAGCAGTGGCAGTAGCCACAGGCGGTGGGGGAGGAAGAAGAGAAGATAGAGGAGAAGGGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45969184..45969285 26863196 MeRIP-seq:(Medium) rs200816873 Functional Loss SNV dbSNP153 33..33 33 - - - 105616 RMVar_ID_105616 Human_SNP_ID_529298411 m1A Human chr13 - 45969309 45969309 45969309 CTGATGAGGATGTCCCTGACCGTACAGAGGTGACAGAAGCAGAGCATACTGCCACCGCCACGACT CTGATGAGGATGTCCCTGACCGTACAGAGGTGTCAGAAGCAGAGCATACTGCCACCGCCACGACT T A ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45969258..45969399 26863196 MeRIP-seq:(Medium) rs1324705606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9367490,Human_RBP_ID_26324076,Human_RBP_ID_27807678 Human_miRNA_ID_2395650,Human_miRNA_ID_2907936,Human_miRNA_ID_3026774 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 105617 RMVar_ID_105617 Human_SNP_ID_529298412 m1A Human chr13 - 45969309 45969309 45969309 CTGATGAGGATGTCCCTGACCGTACAGAGGTGACAGAAGCAGAGCATACTGCCACCGCCACGACT CTGATGAGGATGTCCCTGACCGTACAGAGGTGGCAGAAGCAGAGCATACTGCCACCGCCACGACT T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45969258..45969399 26863196 MeRIP-seq:(Medium) rs1324705606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9367490,Human_RBP_ID_26324076,Human_RBP_ID_27807678 Human_miRNA_ID_2395650,Human_miRNA_ID_2907936,Human_miRNA_ID_3026774 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 105618 RMVar_ID_105618 Human_SNP_ID_529299863 m1A Human chr13 - 45975462 45975444 45975462 AGAGAAGAGAGAGAGAGGGAGAGAGAGCGAGAACGGGAGAGAGAGCGAGAGCGAGAACGGGAACG AGAGAAGAGAGAGAGAGGGAGAGAGAGCGAGA__________________GCGAGAACGGGAACG CTCTCGCTCTCTCTCCCGT C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:45975376..45975763 26863196 MeRIP-seq:(Medium) rs565588902 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_230395,Human_RBP_ID_812484,Human_RBP_ID_5140533,Human_RBP_ID_22919831,Human_RBP_ID_24543557,Human_RBP_ID_24551434,Human_RBP_ID_26324080 RMVar_hsa_circ_73276,RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_266192,RMVar_hsa_circ_71037,RMVar_hsa_circ_269441,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_354279,RMVar_hsa_circ_269492,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_365003,RMVar_hsa_circ_354213,RMVar_hsa_circ_327924 105619 RMVar_ID_105619 Human_SNP_ID_529299870 m1A Human chr13 - 45975462 45975458 45975462 AGAGAAGAGAGAGAGAGGGAGAGAGAGCGAGAACGGGAGAGAGAGCGAGAGCGAGAACGGGAACG AGAGAAGAGAGAGAGAGGGAGAGAGAGCGAGA____GAGAGAGAGCGAGAGCGAGAACGGGAACG CCCGT C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:45975376..45975763 26863196 MeRIP-seq:(Medium) rs1366284237 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_230395,Human_RBP_ID_812484,Human_RBP_ID_5140533,Human_RBP_ID_22919831,Human_RBP_ID_24543557,Human_RBP_ID_24551434,Human_RBP_ID_26324080 RMVar_hsa_circ_73276,RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_266192,RMVar_hsa_circ_71037,RMVar_hsa_circ_269441,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_354279,RMVar_hsa_circ_269492,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_365003,RMVar_hsa_circ_354213,RMVar_hsa_circ_327924 105620 RMVar_ID_105620 Human_SNP_ID_529299874 m1A Human chr13 - 45975465 45975465 45975465 GAAAGAGAAGAGAGAGAGAGGGAGAGAGAGCGAGAACGGGAGAGAGAGCGAGAGCGAGAACGGGA GAAAGAGAAGAGAGAGAGAGGGAGAGAGAGCGGGAACGGGAGAGAGAGCGAGAGCGAGAACGGGA T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:45975415..45975675 26863196 MeRIP-seq:(Medium) rs1566181121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230395,Human_RBP_ID_812484,Human_RBP_ID_4271085,Human_RBP_ID_5140533,Human_RBP_ID_9733583,Human_RBP_ID_17067422,Human_RBP_ID_22919831,Human_RBP_ID_24543557,Human_RBP_ID_24551434,Human_RBP_ID_26324080 RMVar_hsa_circ_73276,RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_266192,RMVar_hsa_circ_71037,RMVar_hsa_circ_269441,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_354279,RMVar_hsa_circ_269492,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_365003,RMVar_hsa_circ_354213,RMVar_hsa_circ_327924 105621 RMVar_ID_105621 Human_SNP_ID_529302359 m1A Human chr13 + 45985590 45985590 45985590 TGCTATAATCTCTCATCTCCCTTGAGTCCCGCATGTCTCTGGAGTCTCTTAGTTCCCTTCGGTCC TGCTATAATCTCTCATCTCCCTTGAGTCCCGCGTGTCTCTGGAGTCTCTTAGTTCCCTTCGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45985540..45985758 26863196 MeRIP-seq:(Medium) rs1276784159 Functional Loss SNV dbSNP153 33..33 33 - - - 105622 RMVar_ID_105622 Human_SNP_ID_529302377 m1A Human chr13 - 45985633 45985633 45985633 AACCTCGAGATGGTCGGGATCGGAGAGATGCCAGAGATACTAGGGACCGAAGGGAACTAAGAGAC AACCTCGAGATGGTCGGGATCGGAGAGATGCCGGAGATACTAGGGACCGAAGGGAACTAAGAGAC T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45985585..45985751 26863196 MeRIP-seq:(Medium) rs1162770813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230399,Human_RBP_ID_812487,Human_RBP_ID_4271125,Human_RBP_ID_6286761,Human_RBP_ID_8790424,Human_RBP_ID_9281230,Human_RBP_ID_9367496,Human_RBP_ID_12168206,Human_RBP_ID_17186957,Human_RBP_ID_24543559,Human_RBP_ID_26324087,Human_RBP_ID_27807935 Human_miRNA_ID_543459,Human_miRNA_ID_578694 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_266192,RMVar_hsa_circ_269441,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_354279,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_365003,RMVar_hsa_circ_354213,RMVar_hsa_circ_327924,RMVar_hsa_circ_163226,RMVar_hsa_circ_80669,RMVar_hsa_circ_310612,RMVar_hsa_circ_351858,RMVar_hsa_circ_353296,RMVar_hsa_circ_368065,RMVar_hsa_circ_352367,RMVar_hsa_circ_340029,RMVar_hsa_circ_91037,RMVar_hsa_circ_163228,RMVar_hsa_circ_163229,RMVar_hsa_circ_163230,RMVar_hsa_circ_163227,RMVar_hsa_circ_163233,RMVar_hsa_circ_339229,RMVar_hsa_circ_355711,RMVar_hsa_circ_356519,RMVar_hsa_circ_361682,RMVar_hsa_circ_348215,RMVar_hsa_circ_299849,RMVar_hsa_circ_304505,RMVar_hsa_circ_163234,RMVar_hsa_circ_163231,RMVar_hsa_circ_163232 105623 RMVar_ID_105623 Human_SNP_ID_529303216 m1A Human chr13 + 45988965 45988965 45988965 GAGCGTCGTAAAGGTGGAGTTAGTGTCCGCTGATAAGATGGTGAAGGAGTTCTTTTTCGACGAGG GAGCGTCGTAAAGGTGGAGTTAGTGTCCGCTGGTAAGATGGTGAAGGAGTTCTTTTTCGACGAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45988916..45989025 26863196 MeRIP-seq:(Medium) rs1302295693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163235,RMVar_hsa_circ_94478 105624 RMVar_ID_105624 Human_SNP_ID_529303218 m1A Human chr13 + 45988970 45988970 45988970 TCGTAAAGGTGGAGTTAGTGTCCGCTGATAAGATGGTGAAGGAGTTCTTTTTCGACGAGGAGAAG TCGTAAAGGTGGAGTTAGTGTCCGCTGATAAGGTGGTGAAGGAGTTCTTTTTCGACGAGGAGAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:45988922..45989002 26863196 MeRIP-seq:(Medium) rs781468199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163235,RMVar_hsa_circ_94478 105625 RMVar_ID_105625 Human_SNP_ID_529306448 m1A Human chr13 - 46003098 46003098 46003098 GATTGTATGTTTTTAACAATATTAACTTTTGTAGAATATAGAATATTTACTTTTCAGAAGCCGTT GATTGTATGTTTTTAACAATATTAACTTTTGTGGAATATAGAATATTTACTTTTCAGAAGCCGTT T C ZC3H13 Ensembl:ENSG00000123200 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:46003095..46003254 26863196 MeRIP-seq:(Medium) rs1229214654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8392685 RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_327924,RMVar_hsa_circ_163226,RMVar_hsa_circ_80669,RMVar_hsa_circ_351858,RMVar_hsa_circ_353296,RMVar_hsa_circ_368065,RMVar_hsa_circ_352367,RMVar_hsa_circ_340029,RMVar_hsa_circ_91037,RMVar_hsa_circ_163228,RMVar_hsa_circ_163229,RMVar_hsa_circ_163227,RMVar_hsa_circ_163233,RMVar_hsa_circ_355711,RMVar_hsa_circ_356519,RMVar_hsa_circ_361682,RMVar_hsa_circ_348215,RMVar_hsa_circ_299849,RMVar_hsa_circ_163234,RMVar_hsa_circ_163232,RMVar_hsa_circ_350908,RMVar_hsa_circ_356868,RMVar_hsa_circ_378171,RMVar_hsa_circ_350526,RMVar_hsa_circ_163237 105626 RMVar_ID_105626 Human_SNP_ID_529318128 m1A Human chr13 - 46052617 46052617 46052617 TCTTCCTGCGACCCAGTTTCGCTTGACCCTGGAGAGGCGGCGGGCGGGTTGGTTCTGCTTCTCAG TCTTCCTGCGACCCAGTTTCGCTTGACCCTGGGGAGGCGGCGGGCGGGTTGGTTCTGCTTCTCAG T C ZC3H13 Ensembl:ENSG00000123200 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:46052567..46052709 26863196 MeRIP-seq:(Medium) rs552313436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5462810,Human_RBP_ID_8392715,Human_RBP_ID_9323466,Human_RBP_ID_17838739,Human_RBP_ID_23126306 RMVar_hsa_circ_163226,RMVar_hsa_circ_91037 105627 RMVar_ID_105627 Human_SNP_ID_529334994 m1A Human chr13 - 46127236 46127236 46127236 TTAATTTTGATATAATCTTTCAAACCAGCTTCATGTGGCTTCCCTTTTCTTTGTTCAAGATGAGG TTAATTTTGATATAATCTTTCAAACCAGCTTCTTGTGGCTTCCCTTTTCTTTGTTCAAGATGAGG T A LCP1 Ensembl:ENSG00000136167 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1409429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_996622,Human_RBP_ID_4271224,Human_RBP_ID_5112232,Human_RBP_ID_6287284,Human_RBP_ID_17476823,Human_RBP_ID_17838753,Human_RBP_ID_18268918 Human_miRNA_ID_433522,Human_miRNA_ID_3004278 GWAS_ID_14093,GWAS_ID_14094 RMVar_hsa_circ_125053,RMVar_hsa_circ_163247 105628 RMVar_ID_105628 Human_SNP_ID_529436803 m1A Human chr13 - 46553244 46553224 46553244 GGAGGGGAGGAGGGTGTGGGCAGGCGCGTAGAATGGGGGGCGGGCGGGGAGGCGGCCGTGGCAGC GGAGGGGAGGAGGGTGTGGGCAGGCGCGTAGA____________________CGGCCGTGGCAGC GCCTCCCCGCCCGCCCCCCAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:46553184..46553396 26863196 MeRIP-seq:(Medium) rs1209327374 Functional Loss DEL dbSNP153 33..52 33 - - - 105629 RMVar_ID_105629 Human_SNP_ID_529436814 m1A Human chr13 - 46553244 46553244 46553244 GGAGGGGAGGAGGGTGTGGGCAGGCGCGTAGAATGGGGGGCGGGCGGGGAGGCGGCCGTGGCAGC GGAGGGGAGGAGGGTGTGGGCAGGCGCGTAGAGTGGGGGGCGGGCGGGGAGGCGGCCGTGGCAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:46553184..46553396 26863196 MeRIP-seq:(Medium) rs1178387927 Functional Loss SNV dbSNP153 33..33 33 - - - 105630 RMVar_ID_105630 Human_SNP_ID_529491730 m1A Human chr13 - 46791419 46791419 46791419 GGAAATTAATGAGATTACTCTTTACTAATAGGAAAAGAATGGCATTGAAGCAGATTTCCAGCAAC GGAAATTAATGAGATTACTCTTTACTAATAGGGAAAGAATGGCATTGAAGCAGATTTCCAGCAAC T C ESD Ensembl:ENSG00000139684 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:46791407..46791472 26863196 MeRIP-seq:(Medium) rs1356438329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879225,Human_RBP_ID_4276972,Human_RBP_ID_9367505,Human_RBP_ID_17245758,Human_RBP_ID_22438422 Human_Splice_Rec_1463496,Human_Splice_Rec_1463497,Human_Splice_Rec_1463512,Human_Splice_Rec_1463513,Human_Splice_Rec_1463538,Human_Splice_Rec_1463539,Human_Splice_Rec_1463552,Human_Splice_Rec_1463553 RMVar_hsa_circ_25834,RMVar_hsa_circ_123524,RMVar_hsa_circ_326820,RMVar_hsa_circ_163287,RMVar_hsa_circ_46802,RMVar_hsa_circ_12119,RMVar_hsa_circ_114891,RMVar_hsa_circ_163289 105631 RMVar_ID_105631 Human_SNP_ID_529794542 m1A Human chr13 - 48059385 48059385 48059385 TTTAATCCTTTTAAAGCATGTTGTGGGATGGGATATTGGCATTGAGCGGGATAAGGGTGATTAGG TTTAATCCTTTTAAAGCATGTTGTGGGATGGGGTATTGGCATTGAGCGGGATAAGGGTGATTAGG T C MED4 Ensembl:ENSG00000136146 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:48059258..48059387 26863196 MeRIP-seq:(Medium) rs182834819 Functional Loss SNV dbSNP153 33..33 33 - - - 105632 RMVar_ID_105632 Human_SNP_ID_529802328 m1A Human chr13 + 48090410 48090410 48090410 ACTTTTGGTTTCTTGAAATTGCCAGCATTTCTATAAGTTCCCTAAAAAAAAAAAACCAACAACAA ACTTTTGGTTTCTTGAAATTGCCAGCATTTCTGTAAGTTCCCTAAAAAAAAAAAACCAACAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:48090351..48090425;chr13:48090351..48090469 26863196 MeRIP-seq:(Medium) rs573939667 Functional Loss SNV dbSNP153 33..33 33 - - - 105633 RMVar_ID_105633 Human_SNP_ID_529802330 m1A Human chr13 - 48090416 48090416 48090416 TTTTTGTTGTTGTTGGTTTTTTTTTTTTAGGGAACTTATAGAAATGCTGGCAATTTCAAGAAACC TTTTTGTTGTTGTTGGTTTTTTTTTTTTAGGGGACTTATAGAAATGCTGGCAATTTCAAGAAACC T C MED4 Ensembl:ENSG00000136146 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:48090351..48090486 26863196 MeRIP-seq:(Medium) rs761827009 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6288874,Human_RBP_ID_18978528 Human_Splice_Rec_1463848,Human_Splice_Rec_1463849,Human_Splice_Rec_1463860,Human_Splice_Rec_1463861,Human_Splice_Rec_1463874,Human_Splice_Rec_1463875 RMVar_hsa_circ_57891,RMVar_hsa_circ_163298,RMVar_hsa_circ_163297,RMVar_hsa_circ_90989,RMVar_hsa_circ_376724,RMVar_hsa_circ_278742,RMVar_hsa_circ_163302,RMVar_hsa_circ_38381,RMVar_hsa_circ_50862 105634 RMVar_ID_105634 Human_SNP_ID_529803613 m1A Human chr13 - 48095048 48095042 48095048 AAATGGCTGCGTCTTCGAGTGGTGAGAAGGAGAAGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCG AAATGGCTGCGTCTTCGAGTGGTGAGAAGGAG______CGGCTGGGAGGCGGTTTGGGAGTGGCG GCTCCTT G MED4 Ensembl:ENSG00000136146 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:48094934..48095131;chr13:48094867..48095100;chr13:48086326..48095100 26863196 MeRIP-seq:(Medium) rs763981876 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_9417545,Human_RBP_ID_18417725 Human_Splice_Rec_1463847,Human_Splice_Rec_1463871 RMVar_hsa_circ_163297,RMVar_hsa_circ_90989 105635 RMVar_ID_105635 Human_SNP_ID_529803613 m1A Human chr13 - 48095047 48095042 48095048 AATGGCTGCGTCTTCGAGTGGTGAGAAGGAGAAGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCGG AATGGCTGCGTCTTCGAGTGGTGAGAAGGAG______CGGCTGGGAGGCGGTTTGGGAGTGGCGG GCTCCTT G MED4 Ensembl:ENSG00000136146 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr13:48094870..48095081;chr13:48094932..48095100 26863196 MeRIP-seq:(Medium) rs763981876 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_9417305,Human_RBP_ID_18417725 Human_Splice_Rec_1463847,Human_Splice_Rec_1463871 RMVar_hsa_circ_163297,RMVar_hsa_circ_90989 105636 RMVar_ID_105636 Human_SNP_ID_529803619 m1A Human chr13 - 48095048 48095048 48095048 AAATGGCTGCGTCTTCGAGTGGTGAGAAGGAGAAGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCG AAATGGCTGCGTCTTCGAGTGGTGAGAAGGAGTAGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCG T A MED4 Ensembl:ENSG00000136146 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:48094934..48095131;chr13:48094867..48095100;chr13:48086326..48095100 26863196 MeRIP-seq:(Medium) rs1566122368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9417545,Human_RBP_ID_18417725 Human_Splice_Rec_1463847,Human_Splice_Rec_1463871 RMVar_hsa_circ_163297,RMVar_hsa_circ_90989 105637 RMVar_ID_105637 Human_SNP_ID_529836186 m1A Human chr13 + 48233351 48233351 48233351 CCGAGCCCGCCGCCGCCCTTCGAGGGCGCCCCAGGCCGCGCCATGGTGAAGGTGACGTTCAACTC CCGAGCCCGCCGCCGCCCTTCGAGGGCGCCCCCGGCCGCGCCATGGTGAAGGTGACGTTCAACTC A C ITM2B Ensembl:ENSG00000136156 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:48233226..48233501 26863196 MeRIP-seq:(Medium) rs552198156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4271507,Human_RBP_ID_9032426,Human_RBP_ID_9281248,Human_RBP_ID_18469380,Human_RBP_ID_18641200,Human_RBP_ID_22438194 105638 RMVar_ID_105638 Human_SNP_ID_529836187 m1A Human chr13 + 48233351 48233351 48233351 CCGAGCCCGCCGCCGCCCTTCGAGGGCGCCCCAGGCCGCGCCATGGTGAAGGTGACGTTCAACTC CCGAGCCCGCCGCCGCCCTTCGAGGGCGCCCCGGGCCGCGCCATGGTGAAGGTGACGTTCAACTC A G ITM2B Ensembl:ENSG00000136156 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:48233226..48233501 26863196 MeRIP-seq:(Medium) rs552198156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4271507,Human_RBP_ID_9032426,Human_RBP_ID_9281248,Human_RBP_ID_18469380,Human_RBP_ID_18641200,Human_RBP_ID_22438194 105639 RMVar_ID_105639 Human_SNP_ID_529852833 m1A Human chr13 + 48303906 48303906 48303906 TCCTCCACAGCTCGCTGGCTCCCGCCGCGGAAAGGCGTCATGCCGCCCAAAACCCCCCGAAAAAC TCCTCCACAGCTCGCTGGCTCCCGCCGCGGAAGGGCGTCATGCCGCCCAAAACCCCCCGAAAAAC A G RB1 Ensembl:ENSG00000139687 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:48303858..48304015 26863196 MeRIP-seq:(Medium) rs1566174023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276623,Human_RBP_ID_9281249 105640 RMVar_ID_105640 Human_SNP_ID_529852840 m1A Human chr13 + 48303922 48303921 48303922 GGCTCCCGCCGCGGAAAGGCGTCATGCCGCCCAAAACCCCCCGAAAAACGGCCGCCACCGCCGCC GGCTCCCGCCGCGGAAAGGCGTCATGCCGCCC_AAACCCCCCGAAAAACGGCCGCCACCGCCGCC CA C RB1 Ensembl:ENSG00000139687 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:48303750..48307329 26863196 MeRIP-seq:(Medium) rs1226865525 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4276623,Human_RBP_ID_9281249 105641 RMVar_ID_105641 Human_SNP_ID_529852875 m1A Human chr13 + 48303969 48303969 48303969 ACGGCCGCCACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCACCGCCGCCGCCGCCCCCTCCTGA ACGGCCGCCACCGCCGCCGCTGCCGCCGCGGACCCCCCGGCACCGCCGCCGCCGCCCCCTCCTGA A C RB1 Ensembl:ENSG00000139687 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA chr13:48303874..48304050;chr13:48303900..48304022 26863196 MeRIP-seq:(Medium) rs1046808421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276623,Human_RBP_ID_22532552 Human_Splice_Rec_1463997,Human_Splice_Rec_1464049,Human_Splice_Rec_1464053,Human_Splice_Rec_1464105,Human_Splice_Rec_1464117 105642 RMVar_ID_105642 Human_SNP_ID_529852884 m1A Human chr13 + 48303978 48303976 48303979 ACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCACCGCCGCCGCCGCCCCCTCCTGAGGAGGACCC ACCGCCGCCGCTGCCGCCGCGGAACCCCCGG___CGCCGCCGCCGCCCCCTCCTGAGGAGGACCC GCAC G RB1 Ensembl:ENSG00000139687 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:48303800..48304050 26863196 MeRIP-seq:(Medium) rs1298675805 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8792069,Human_RBP_ID_22532552 Human_Splice_Rec_1463997,Human_Splice_Rec_1464049,Human_Splice_Rec_1464053,Human_Splice_Rec_1464105,Human_Splice_Rec_1464117 105643 RMVar_ID_105643 Human_SNP_ID_529852887 m1A Human chr13 + 48303978 48303978 48303978 ACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCACCGCCGCCGCCGCCCCCTCCTGAGGAGGACCC ACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCCCCGCCGCCGCCGCCCCCTCCTGAGGAGGACCC A C RB1 Ensembl:ENSG00000139687 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:48303800..48304050 26863196 MeRIP-seq:(Medium) rs1014225642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8792069,Human_RBP_ID_22532552 Human_Splice_Rec_1463997,Human_Splice_Rec_1464049,Human_Splice_Rec_1464053,Human_Splice_Rec_1464105,Human_Splice_Rec_1464117 105644 RMVar_ID_105644 Human_SNP_ID_529852888 m1A Human chr13 + 48303978 48303978 48303978 ACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCACCGCCGCCGCCGCCCCCTCCTGAGGAGGACCC ACCGCCGCCGCTGCCGCCGCGGAACCCCCGGCGCCGCCGCCGCCGCCCCCTCCTGAGGAGGACCC A G RB1 Ensembl:ENSG00000139687 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:48303800..48304050 26863196 MeRIP-seq:(Medium) rs1014225642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8792069,Human_RBP_ID_22532552 Human_Splice_Rec_1463997,Human_Splice_Rec_1464049,Human_Splice_Rec_1464053,Human_Splice_Rec_1464105,Human_Splice_Rec_1464117 105645 RMVar_ID_105645 Human_SNP_ID_530010411 m1A Human chr13 - 48975826 48975826 48975826 GCCCGCGGCCGGGACCCCGAACCCCCGCCTCGAGCCCGCCGCGCCGGGGCTCTCTCACCGGAACG GCCCGCGGCCGGGACCCCGAACCCCCGCCTCGGGCCCGCCGCGCCGGGGCTCTCTCACCGGAACG T C AL161421.1 Ensembl:ENSG00000275202 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:48975731..48975876 26863410 MeRIP-seq:(Medium) rs1427538682 Functional Loss SNV dbSNP153 33..33 33 - - - 105646 RMVar_ID_105646 Human_SNP_ID_530010490 m1A Human chr13 + 48975972 48975972 48975972 GGCGGCGTTCGTGGTCCCTCGGGTGAAACAGAAAGCGGGAGCTACGCGGAGAGGGAGCGAAGAGC GGCGGCGTTCGTGGTCCCTCGGGTGAAACAGAGAGCGGGAGCTACGCGGAGAGGGAGCGAAGAGC A G FNDC3A Ensembl:ENSG00000102531 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:48975923..48976819 26863196 MeRIP-seq:(Medium) rs1215643394 Functional Loss SNV dbSNP153 33..33 33 - - - 105647 RMVar_ID_105647 Human_SNP_ID_530076227 m1A Human chr13 - 49248831 49248831 49248831 AGAGACGACAAACACTTTAAACTTTGTTACTAATGGTGAAAAAGGGAGCCAATCTCAATGCCACT AGAGACGACAAACACTTTAAACTTTGTTACTACTGGTGAAAAAGGGAGCCAATCTCAATGCCACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:49248829..49248905 26863196 MeRIP-seq:(Medium) rs1312198031 Functional Loss SNV dbSNP153 33..33 33 - - - 105648 RMVar_ID_105648 Human_SNP_ID_530140867 m1A Human chr13 + 49527314 49527314 49527314 CACACAGCTGGGCAGGCCGGGCACAGAGTCAAACAGCATTGGTGGATGGCTCCCCCTGAAGTTGC CACACAGCTGGGCAGGCCGGGCACAGAGTCAAGCAGCATTGGTGGATGGCTCCCCCTGAAGTTGC A G PHF11 Ensembl:ENSG00000136147 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:49527304..49527382 32194978 MeRIP-seq:(Medium) rs935895399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92415,RMVar_hsa_circ_163390 105649 RMVar_ID_105649 Human_SNP_ID_530142181 m1A Human chr13 - 49533153 49533153 49533153 AAGAAGTGGTTCTTCAAGTCAACCCTCTTACAAGACTTAGTGGAATTTGCTTTATCTACTTTAGG AAGAAGTGGTTCTTCAAGTCAACCCTCTTACAGGACTTAGTGGAATTTGCTTTATCTACTTTAGG T C RCBTB1 Ensembl:ENSG00000136144 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1046028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23598631,Human_RBP_ID_27640236 GWAS_ID_14095,GWAS_ID_14096,GWAS_ID_14097,GWAS_ID_14098,GWAS_ID_14099,GWAS_ID_14100,GWAS_ID_14101,GWAS_ID_14102,GWAS_ID_14103,GWAS_ID_14104,GWAS_ID_14105,GWAS_ID_14106,GWAS_ID_14107,GWAS_ID_14108,GWAS_ID_14109,GWAS_ID_14110,GWAS_ID_14111,GWAS_ID_14112,GWAS_ID_14113,GWAS_ID_14114,GWAS_ID_14115,GWAS_ID_14116,GWAS_ID_14117,GWAS_ID_14118,GWAS_ID_14119,GWAS_ID_14120,GWAS_ID_14121,GWAS_ID_14122,GWAS_ID_14123,GWAS_ID_14124,GWAS_ID_14125,GWAS_ID_14126,GWAS_ID_14127,GWAS_ID_14128,GWAS_ID_14129,GWAS_ID_14130,GWAS_ID_14131,GWAS_ID_14132,GWAS_ID_14133,GWAS_ID_14134,GWAS_ID_14135,GWAS_ID_14136,GWAS_ID_14137,GWAS_ID_14138,GWAS_ID_14139,GWAS_ID_14140,GWAS_ID_14141,GWAS_ID_14142,GWAS_ID_14143,GWAS_ID_14144,GWAS_ID_14145,GWAS_ID_14146,GWAS_ID_14147,GWAS_ID_14148,GWAS_ID_14149,GWAS_ID_14150,GWAS_ID_14151,GWAS_ID_14152,GWAS_ID_14153,GWAS_ID_14154,GWAS_ID_14155,GWAS_ID_14156,GWAS_ID_14157,GWAS_ID_14158,GWAS_ID_14159,GWAS_ID_14160,GWAS_ID_14161,GWAS_ID_14162,GWAS_ID_14163,GWAS_ID_14164,GWAS_ID_14165,GWAS_ID_14166,GWAS_ID_14167,GWAS_ID_14168,GWAS_ID_14169,GWAS_ID_14170,GWAS_ID_14171,GWAS_ID_14172,GWAS_ID_14173,GWAS_ID_14174,GWAS_ID_14175,GWAS_ID_14176 RMVar_hsa_circ_94516,RMVar_hsa_circ_163392 105650 RMVar_ID_105650 Human_SNP_ID_530142401 m1A Human chr13 - 49534116 49534116 49534116 AGTAAATGTGGAGCCTTTAAGAACTGAAGCGCAAGGCTGCTGGGTTCTGTGTGAGTGCTCTGGGG AGTAAATGTGGAGCCTTTAAGAACTGAAGCGCGAGGCTGCTGGGTTCTGTGTGAGTGCTCTGGGG T C RCBTB1 Ensembl:ENSG00000136144 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7317982 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_2450628,Human_miRNA_ID_2540070 GWAS_ID_14177,GWAS_ID_14178,GWAS_ID_14179,GWAS_ID_14180,GWAS_ID_14181,GWAS_ID_14182,GWAS_ID_14183,GWAS_ID_14184,GWAS_ID_14185,GWAS_ID_14186,GWAS_ID_14187,GWAS_ID_14188,GWAS_ID_14189,GWAS_ID_14190,GWAS_ID_14191,GWAS_ID_14192,GWAS_ID_14193,GWAS_ID_14194,GWAS_ID_14195,GWAS_ID_14196,GWAS_ID_14197,GWAS_ID_14198,GWAS_ID_14199,GWAS_ID_14200,GWAS_ID_14201,GWAS_ID_14202,GWAS_ID_14203,GWAS_ID_14204,GWAS_ID_14205,GWAS_ID_14206,GWAS_ID_14207,GWAS_ID_14208,GWAS_ID_14209,GWAS_ID_14210,GWAS_ID_14211,GWAS_ID_14212,GWAS_ID_14213,GWAS_ID_14214,GWAS_ID_14215,GWAS_ID_14216,GWAS_ID_14217,GWAS_ID_14218,GWAS_ID_14219,GWAS_ID_14220,GWAS_ID_14221,GWAS_ID_14222,GWAS_ID_14223,GWAS_ID_14224,GWAS_ID_14225,GWAS_ID_14226,GWAS_ID_14227,GWAS_ID_14228,GWAS_ID_14229,GWAS_ID_14230,GWAS_ID_14231,GWAS_ID_14232,GWAS_ID_14233,GWAS_ID_14234,GWAS_ID_14235,GWAS_ID_14236,GWAS_ID_14237,GWAS_ID_14238,GWAS_ID_14239,GWAS_ID_14240,GWAS_ID_14241,GWAS_ID_14242,GWAS_ID_14243,GWAS_ID_14244,GWAS_ID_14245,GWAS_ID_14246,GWAS_ID_14247,GWAS_ID_14248,GWAS_ID_14249,GWAS_ID_14250,GWAS_ID_14251,GWAS_ID_14252,GWAS_ID_14253,GWAS_ID_14254,GWAS_ID_14255,GWAS_ID_14256,GWAS_ID_14257,GWAS_ID_14258 RMVar_hsa_circ_94516,RMVar_hsa_circ_163392 105651 RMVar_ID_105651 Human_SNP_ID_530182046 m1A Human chr13 + 49691342 49691330 49691343 CCGCCCCCTGCCCGCGGCCCAGGCGCAGGCCCAGGGCGCAGCCCGCCGCCAGCAGCGCGGCGCAC CCGCCCCCTGCCCGCGGCCCA_____________GGCGCAGCCCGCCGCCAGCAGCGCGGCGCAC AGGCGCAGGCCCAG A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:49691251..49691425 26863410 MeRIP-seq:(Medium) rs754895213 Functional Loss DEL dbSNP153 22..34 33 - - - 105652 RMVar_ID_105652 Human_SNP_ID_530182092 m1A Human chr13 + 49691416 49691416 49691416 GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCAGCGCCCATGCTTCAGGCTTCCGACGCCAACGG GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCGGCGCCCATGCTTCAGGCTTCCGACGCCAACGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:49691251..49691475;chr13:49669838..49691475 26863196 MeRIP-seq:(Medium) rs911699272 Functional Loss SNV dbSNP153 33..33 33 - - - 105653 RMVar_ID_105653 Human_SNP_ID_530182093 m1A Human chr13 + 49691416 49691416 49691416 GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCAGCGCCCATGCTTCAGGCTTCCGACGCCAACGG GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCTGCGCCCATGCTTCAGGCTTCCGACGCCAACGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:49691251..49691475;chr13:49669838..49691475 26863196 MeRIP-seq:(Medium) rs911699272 Functional Loss SNV dbSNP153 33..33 33 - - - 105654 RMVar_ID_105654 Human_SNP_ID_530196322 m1A Human chr13 + 49746979 49746979 49746979 ACCTTCCGCAGTTCCACTGTCACTTCATTTCTATGTCTTCGCATTGTCTAGAAAAGAAAAACAAA ACCTTCCGCAGTTCCACTGTCACTTCATTTCTGTGTCTTCGCATTGTCTAGAAAAGAAAAACAAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:49733027..49792574 26863196 MeRIP-seq:(Medium) rs1423370302 Functional Loss SNV dbSNP153 33..33 33 - - - 105655 RMVar_ID_105655 Human_SNP_ID_530207777 m1A Human chr13 - 49792499 49792499 49792499 GCCGCCGCCGGAGCCGCGCGCAGCCATGGCCGAGAACCCCAGCTTGGAGAACCACCGCATCAAGA GCCGCCGCCGGAGCCGCGCGCAGCCATGGCCGGGAACCCCAGCTTGGAGAACCACCGCATCAAGA T C KPNA3 Ensembl:ENSG00000102753 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:49792396..49792575;chr13:49792378..49792573 26863196 MeRIP-seq:(Medium) rs762963084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276628,Human_RBP_ID_6290972,Human_RBP_ID_8790589,Human_RBP_ID_9281250,Human_RBP_ID_9367526,Human_RBP_ID_18936371 Human_Splice_Rec_1465163 Human_miRNA_ID_2685075,Human_miRNA_ID_2789714,Human_miRNA_ID_2819328 RMVar_hsa_circ_163403,RMVar_hsa_circ_77144 105656 RMVar_ID_105656 Human_SNP_ID_530207794 m1A Human chr13 - 49792520 49792520 49792520 GCCGCCGCAGCCGCAGGAGTAGCCGCCGCCGGAGCCGCGCGCAGCCATGGCCGAGAACCCCAGCT GCCGCCGCAGCCGCAGGAGTAGCCGCCGCCGGCGCCGCGCGCAGCCATGGCCGAGAACCCCAGCT T G KPNA3 Ensembl:ENSG00000102753 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr13:49746951..49792660;chr13:49792448..49792580 26863196 MeRIP-seq:(Medium) rs754028944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276628,Human_RBP_ID_9281250,Human_RBP_ID_9367526,Human_RBP_ID_18936371 Human_Splice_Rec_1465163 RMVar_hsa_circ_163403,RMVar_hsa_circ_77144 105657 RMVar_ID_105657 Human_SNP_ID_530241662 m1A Human chr13 - 49928074 49928074 49928074 TTTAAACTGTTATATTTTTAGGAATCTGGGGTATTGGTGTTGCAACTCAGAAGGTTAACTTGAAT TTTAAACTGTTATATTTTTAGGAATCTGGGGTGTTGGTGTTGCAACTCAGAAGGTTAACTTGAAT T C SPRYD7 Ensembl:ENSG00000123178 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:49928024..49928121 26863196 MeRIP-seq:(Medium) rs755008423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4272025,Human_RBP_ID_12178027,Human_RBP_ID_17839457,Human_RBP_ID_18641465,Human_RBP_ID_26324100 Human_Splice_Rec_1465204,Human_Splice_Rec_1465210,Human_Splice_Rec_1465216 RMVar_hsa_circ_163423,RMVar_hsa_circ_78691,RMVar_hsa_circ_163421,RMVar_hsa_circ_281870,RMVar_hsa_circ_322044,RMVar_hsa_circ_163424,RMVar_hsa_circ_163425,RMVar_hsa_circ_303798 105658 RMVar_ID_105658 Human_SNP_ID_530243505 m1A Human chr13 + 49936282 49936282 49936282 CGACTCCGCCGCCGTCCCTAGACCGAGGCGACACTGCCCCCCGCCGCTCAGCTCCGTCTCCTGCC CGACTCCGCCGCCGTCCCTAGACCGAGGCGACGCTGCCCCCCGCCGCTCAGCTCCGTCTCCTGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr13:49936126..49936325;chr13:49936126..49936390 26863196 MeRIP-seq:(Medium) rs200866128 Functional Loss SNV dbSNP153 33..33 33 - - - 105659 RMVar_ID_105659 Human_SNP_ID_530254538 m1A Human chr13 + 49987004 49987004 49987004 AGCCTGCCTAGTATCAGAGGCACTCCCTGCCCAGTGTCACATGGGCAGTCATTTAACAGCCATGA AGCCTGCCTAGTATCAGAGGCACTCCCTGCCCGGTGTCACATGGGCAGTCATTTAACAGCCATGA A G lnc-TRIM13-2 RNACentral:URS00008B3ADA lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:49986957..49987041 26863196 MeRIP-seq:(Medium) rs1390269100 Functional Loss SNV dbSNP153 33..33 33 - - - 105660 RMVar_ID_105660 Human_SNP_ID_530278307 m1A Human chr13 + 50081320 50081320 50081320 GGCGGTGGCGGGGGGGACTGTTGCCACGACCCACCGGAGGGACCCATGACTCCGGGTCCTGAATT GGCGGTGGCGGGGGGGACTGTTGCCACGACCCGCCGGAGGGACCCATGACTCCGGGTCCTGAATT A G lnc-KCNRG-2 RNACentral:URS00008B5444 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:50081269..50081444 32194978 MeRIP-seq:(Medium) rs1350617601 Functional Loss SNV dbSNP153 33..33 33 - - - 105661 RMVar_ID_105661 Human_SNP_ID_530278439 m1A Human chr13 + 50081726 50081726 50081726 CTACTTCCTCGGATTTTTCGCGATTAAGTGAGAGTAGACCCCGCGCCCACTCCCTGCACCCACCA CTACTTCCTCGGATTTTTCGCGATTAAGTGAGCGTAGACCCCGCGCCCACTCCCTGCACCCACCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:50081518..50081792 26863196 MeRIP-seq:(Medium) rs1223564685 Functional Loss SNV dbSNP153 33..33 33 - - - 105662 RMVar_ID_105662 Human_SNP_ID_530278652 m1A Human chr13 - 50082322 50082322 50082322 CTCCAACGTAGACTAAATGCCTGTGGGCTGGTAGCTATAAGACGACCCCTCGGCCCCACAACCTC CTCCAACGTAGACTAAATGCCTGTGGGCTGGTGGCTATAAGACGACCCCTCGGCCCCACAACCTC T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:50082271..50082394 26863196 MeRIP-seq:(Medium) rs751186653 Functional Loss SNV dbSNP153 33..33 33 - - - 105663 RMVar_ID_105663 Human_SNP_ID_530278661 m1A Human chr13 - 50082350 50082350 50082350 CTCCTAAGCAGGACCCGTATTTGTTTACCTCCAACGTAGACTAAATGCCTGTGGGCTGGTAGCTA CTCCTAAGCAGGACCCGTATTTGTTTACCTCCGACGTAGACTAAATGCCTGTGGGCTGGTAGCTA T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:50082300..50082407 26863196 MeRIP-seq:(Medium) rs1240857356 Functional Loss SNV dbSNP153 33..33 33 - - - 105664 RMVar_ID_105664 Human_SNP_ID_530278662 m1A Human chr13 + 50082353 50082353 50082353 CTACCAGCCCACAGGCATTTAGTCTACGTTGGAGGTAAACAAATACGGGTCCTGCTTAGGAGAAA CTACCAGCCCACAGGCATTTAGTCTACGTTGGCGGTAAACAAATACGGGTCCTGCTTAGGAGAAA A C DLEU1,AL137060.6 Ensembl:ENSG00000176124,Ensembl:ENSG00000276089 lincRNA,Other exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:50082305..50082400 32194978 MeRIP-seq:(Medium) rs1011048927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_996783,Human_RBP_ID_1485317,Human_RBP_ID_1810675,Human_RBP_ID_4276633,Human_RBP_ID_5562701,Human_RBP_ID_9032975,Human_RBP_ID_18417730,Human_RBP_ID_22494746,Human_RBP_ID_26324103 Human_miRNA_ID_3146108,Human_miRNA_ID_3216682,Human_miRNA_ID_3216696 105665 RMVar_ID_105665 Human_SNP_ID_530280990 m1A Human chr13 + 50093129 50093129 50093129 CAAGTTTGAGTTGAAGTAAGATGGTACAAAATATATGCTCTAGGTAATGGGAGAGGGAATTAATG CAAGTTTGAGTTGAAGTAAGATGGTACAAAATGTATGCTCTAGGTAATGGGAGAGGGAATTAATG A G DLEU1 Ensembl:ENSG00000176124 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:50093124..50093286 26863196 MeRIP-seq:(Medium) rs1412826877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123422,RMVar_hsa_circ_163444 105666 RMVar_ID_105666 Human_SNP_ID_530419743 m1A Human chr13 + 50715493 50715493 50715493 GCCGGTGGCAGCTAAAGGAGAAAGGGGGCGAGAGCTGGAGAAGTCGCACTTCCGCCGATGGCGCA GCCGGTGGCAGCTAAAGGAGAAAGGGGGCGAGTGCTGGAGAAGTCGCACTTCCGCCGATGGCGCA A T DLEU1 Ensembl:ENSG00000176124 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:50715404..50715661 26863196 MeRIP-seq:(Medium) rs377165047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22354707 105667 RMVar_ID_105667 Human_SNP_ID_530419794 m1A Human chr13 - 50715712 50715712 50715712 AATCTTCGGAGTTTTTCCGAAACACCTCCACTAGGGAGCTGCCATTGTAGCTTCCTAACACACGT AATCTTCGGAGTTTTTCCGAAACACCTCCACTGGGGAGCTGCCATTGTAGCTTCCTAACACACGT T C DLEU7 Ensembl:ENSG00000186047 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:50715663..50715748 26863410 MeRIP-seq:(Medium) rs1312864588 Functional Loss SNV dbSNP153 33..33 33 - - - 105668 RMVar_ID_105668 Human_SNP_ID_530536074 m1A Human chr13 + 51222493 51222493 51222493 ACGACGGCGCCCGCAAGCCGAGCGCGGCCGGGACGTGCACCATGGACCCAAAGGCGGGCGGCGGC ACGACGGCGCCCGCAAGCCGAGCGCGGCCGGGGCGTGCACCATGGACCCAAAGGCGGGCGGCGGC A G FAM124A Ensembl:ENSG00000150510 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:51222396..51222575 26863196 MeRIP-seq:(Medium) rs1187299694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1466655,Human_Splice_Rec_1466659,Human_Splice_Rec_1466667,Human_Splice_Rec_1466671 105669 RMVar_ID_105669 Human_SNP_ID_530536094 m1A Human chr13 + 51222533 51222533 51222533 CATGGACCCAAAGGCGGGCGGCGGCGGCGAGGAGGACGACTGCGTGGACTCGGGCGCCGAGACCG CATGGACCCAAAGGCGGGCGGCGGCGGCGAGGGGGACGACTGCGTGGACTCGGGCGCCGAGACCG A G FAM124A Ensembl:ENSG00000150510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:51222368..51222543;chr13:51222352..51225160;chr13:51222334..51222751 26863196 MeRIP-seq:(Medium) rs1282222658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1466655,Human_Splice_Rec_1466659,Human_Splice_Rec_1466667,Human_Splice_Rec_1466671 105670 RMVar_ID_105670 Human_SNP_ID_530548600 m1A Human chr13 + 51281065 51281065 51281065 CAGAGGCCTCCTGGGCTTCCCTCCCTTTCTTCACCAAAAGGTCTTCCAGCTCCTCAGCGACAGCT CAGAGGCCTCCTGGGCTTCCCTCCCTTTCTTCGCCAAAAGGTCTTCCAGCTCCTCAGCGACAGCT A G FAM124A Ensembl:ENSG00000150510 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:51281014..51281120 26863196 MeRIP-seq:(Medium) rs1239552873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27428238 105671 RMVar_ID_105671 Human_SNP_ID_530569366 m1A Human chr13 - 51372372 51372372 51372372 AGCTAGGAGAAAATAGGGGAGAATTTAATGTCATGGAAGCTAAAGGGCAAGATAATTGAGTGGGT AGCTAGGAGAAAATAGGGGAGAATTTAATGTCTTGGAAGCTAAAGGGCAAGATAATTGAGTGGGT T A INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51372370..51372765 26863196 MeRIP-seq:(Medium) rs940733185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2128,RMVar_hsa_circ_98836,RMVar_hsa_circ_163474,RMVar_hsa_circ_57392,RMVar_hsa_circ_356109,RMVar_hsa_circ_163476,RMVar_hsa_circ_279909,RMVar_hsa_circ_54119 105672 RMVar_ID_105672 Human_SNP_ID_530569367 m1A Human chr13 - 51372372 51372372 51372372 AGCTAGGAGAAAATAGGGGAGAATTTAATGTCATGGAAGCTAAAGGGCAAGATAATTGAGTGGGT AGCTAGGAGAAAATAGGGGAGAATTTAATGTCGTGGAAGCTAAAGGGCAAGATAATTGAGTGGGT T C INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51372370..51372765 26863196 MeRIP-seq:(Medium) rs940733185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2128,RMVar_hsa_circ_98836,RMVar_hsa_circ_163474,RMVar_hsa_circ_57392,RMVar_hsa_circ_356109,RMVar_hsa_circ_163476,RMVar_hsa_circ_279909,RMVar_hsa_circ_54119 105673 RMVar_ID_105673 Human_SNP_ID_530574142 m1A Human chr13 - 51392515 51392515 51392515 CTCTCTATATATTTGGAAGCAACAGGAAGGCTAGCATGGCTGGAGCTTACATAGGGAGGAATAGA CTCTCTATATATTTGGAAGCAACAGGAAGGCTTGCATGGCTGGAGCTTACATAGGGAGGAATAGA T A INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51392497..51392619 26863196 MeRIP-seq:(Medium) rs934349593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98836,RMVar_hsa_circ_163474,RMVar_hsa_circ_57392,RMVar_hsa_circ_356109,RMVar_hsa_circ_163476,RMVar_hsa_circ_163480,RMVar_hsa_circ_11544,RMVar_hsa_circ_15995,RMVar_hsa_circ_290803,RMVar_hsa_circ_12098,RMVar_hsa_circ_73105,RMVar_hsa_circ_347827,RMVar_hsa_circ_56750 105674 RMVar_ID_105674 Human_SNP_ID_530574143 m1A Human chr13 - 51392515 51392515 51392515 CTCTCTATATATTTGGAAGCAACAGGAAGGCTAGCATGGCTGGAGCTTACATAGGGAGGAATAGA CTCTCTATATATTTGGAAGCAACAGGAAGGCTGGCATGGCTGGAGCTTACATAGGGAGGAATAGA T C INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51392497..51392619 26863196 MeRIP-seq:(Medium) rs934349593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98836,RMVar_hsa_circ_163474,RMVar_hsa_circ_57392,RMVar_hsa_circ_356109,RMVar_hsa_circ_163476,RMVar_hsa_circ_163480,RMVar_hsa_circ_11544,RMVar_hsa_circ_15995,RMVar_hsa_circ_290803,RMVar_hsa_circ_12098,RMVar_hsa_circ_73105,RMVar_hsa_circ_347827,RMVar_hsa_circ_56750 105675 RMVar_ID_105675 Human_SNP_ID_530588533 m1A Human chr13 + 51452017 51452017 51452017 GCATAGGGCGGCTCTTCGAAAGTGACCAGCATATACCTGTCTCCTCTGCTGGCAGGGTCCCGGGC GCATAGGGCGGCTCTTCGAAAGTGACCAGCATGTACCTGTCTCCTCTGCTGGCAGGGTCCCGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:51451966..51452265 26863196 MeRIP-seq:(Medium) rs1279044672 Functional Loss SNV dbSNP153 33..33 33 - - - 105676 RMVar_ID_105676 Human_SNP_ID_530588855 m1A Human chr13 - 51452835 51452835 51452835 CGTCTCCCGCTGGGACACACACAGGGGCCGGGAGCGGGGACGGGACCCCCGAGGCGGGGGGGACG CGTCTCCCGCTGGGACACACACAGGGGCCGGGGGCGGGGACGGGACCCCCGAGGCGGGGGGGACG T C INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:51452785..51452856 26863196 MeRIP-seq:(Medium) rs1214026801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756321,Human_RBP_ID_5315335,Human_RBP_ID_9417553,Human_RBP_ID_21968414 105677 RMVar_ID_105677 Human_SNP_ID_530588858 m1A Human chr13 - 51452845 51452843 51452845 GAGCCAGGCCCGTCTCCCGCTGGGACACACACAGGGGCCGGGAGCGGGGACGGGACCCCCGAGGC GAGCCAGGCCCGTCTCCCGCTGGGACACACAC__GGGCCGGGAGCGGGGACGGGACCCCCGAGGC CCT C INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:51452825..51452951 26863196 MeRIP-seq:(Medium) rs1277104979 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_756321,Human_RBP_ID_4279400,Human_RBP_ID_5315335,Human_RBP_ID_9323623,Human_RBP_ID_9417553,Human_RBP_ID_21968414 105678 RMVar_ID_105678 Human_SNP_ID_530591166 m1A Human chr13 + 51461046 51461046 51461046 TTTGGAGACTGGCAAGATTACTGATTTCATCAAATTCGACACTGGTCACCTGTGTATGGTGACTG TTTGGAGACTGGCAAGATTACTGATTTCATCAGATTCGACACTGGTCACCTGTGTATGGTGACTG A G RPS4XP16,INTS6-AS1 Ensembl:ENSG00000224892,Ensembl:ENSG00000236778 Pseudogene,lincRNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1011996560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1837517,Human_miRNA_ID_1837946,Human_miRNA_ID_1894449 105679 RMVar_ID_105679 Human_SNP_ID_530621609 m1A Human chr13 + 51584669 51584645 51584669 CGGCCCCGCGGCGCGGTTGGCGGCGGCGCCCCAGGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT CGGCCCCGC________________________GGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT CGGCGCGGTTGGCGGCGGCGCCCCA C WDFY2 Ensembl:ENSG00000139668 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:51584629..51584818 26863196 MeRIP-seq:(Medium) rs778373656 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_230460,Human_RBP_ID_4272277,Human_RBP_ID_17840068,Human_RBP_ID_18978548 RMVar_hsa_circ_103275,RMVar_hsa_circ_163485 105680 RMVar_ID_105680 Human_SNP_ID_530621626 m1A Human chr13 + 51584669 51584669 51584669 CGGCCCCGCGGCGCGGTTGGCGGCGGCGCCCCAGGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT CGGCCCCGCGGCGCGGTTGGCGGCGGCGCCCCCGGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT A C WDFY2 Ensembl:ENSG00000139668 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:51584629..51584818 26863196 MeRIP-seq:(Medium) rs1363663990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230460,Human_RBP_ID_4272277,Human_RBP_ID_17840068,Human_RBP_ID_18978548 RMVar_hsa_circ_103275,RMVar_hsa_circ_163485 105681 RMVar_ID_105681 Human_SNP_ID_530621627 m1A Human chr13 + 51584669 51584669 51584669 CGGCCCCGCGGCGCGGTTGGCGGCGGCGCCCCAGGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT CGGCCCCGCGGCGCGGTTGGCGGCGGCGCCCCTGGCGCGCCCCCTCCTCCGATGGCGGCGGAGAT A T WDFY2 Ensembl:ENSG00000139668 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:51584629..51584818 26863196 MeRIP-seq:(Medium) rs1363663990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230460,Human_RBP_ID_4272277,Human_RBP_ID_17840068,Human_RBP_ID_18978548 RMVar_hsa_circ_103275,RMVar_hsa_circ_163485 105682 RMVar_ID_105682 Human_SNP_ID_530659881 m1A Human chr13 - 51751417 51751417 51751417 CACAGGGCCCACCCCACCCTGCTGTGCCACCTACCTCCTGCCTCTCCACGTCCATGTTCCAGACG CACAGGGCCCACCCCACCCTGCTGTGCCACCTCCCTCCTGCCTCTCCACGTCCATGTTCCAGACG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:51751387..51751487 26863196 MeRIP-seq:(Medium) rs78760921 Functional Loss SNV dbSNP153 33..33 33 - - - 105683 RMVar_ID_105683 Human_SNP_ID_530662843 m1A Human chr13 - 51764282 51764282 51764282 TGGCATGCCTCTATCATAACCACATTGCACTGAAAAGACCCATTTACTCACTGTGTGACCTCTGC TGGCATGCCTCTATCATAACCACATTGCACTGGAAAGACCCATTTACTCACTGTGTGACCTCTGC T C AL162377.3 Ensembl:ENSG00000285444 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51764231..51764407 26863196 MeRIP-seq:(Medium) rs1232917918 Functional Loss SNV dbSNP153 33..33 33 - - - 105684 RMVar_ID_105684 Human_SNP_ID_530704851 m1A Human chr13 - 51937392 51937392 51937392 CCCTTCCTCACTGTGTGCTCCTCTCCATCAGAATGATTTGCTGGATGTGGTGGCTAGCATTCACC CCCTTCCTCACTGTGTGCTCCTCTCCATCAGAGTGATTTGCTGGATGTGGTGGCTAGCATTCACC T C ATP7B Ensembl:ENSG00000123191 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:51937381..51937509 26863410 MeRIP-seq:(Medium) rs1323977909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5350841,Human_RBP_ID_19062177 Human_Splice_Rec_1467392,Human_Splice_Rec_1467418,Human_Splice_Rec_1467448,Human_Splice_Rec_1467480,Human_Splice_Rec_1467494,Human_Splice_Rec_1467502,Human_Splice_Rec_1467538,Human_Splice_Rec_1467578,Human_Splice_Rec_1467606,Human_Splice_Rec_1467630,Human_Splice_Rec_1467670,Human_Splice_Rec_1467708,Human_Splice_Rec_1467748,Human_Splice_Rec_1467786,Human_Splice_Rec_1467828 RMVar_hsa_circ_11469,RMVar_hsa_circ_51395,RMVar_hsa_circ_335893,RMVar_hsa_circ_353470,RMVar_hsa_circ_269795,RMVar_hsa_circ_55421,RMVar_hsa_circ_19930,RMVar_hsa_circ_163503,RMVar_hsa_circ_163504 105685 RMVar_ID_105685 Human_SNP_ID_530723905 m1A Human chr13 - 52012037 52012037 52012037 CCGTTGGAGGCCATTGGCTGGCCTTTGCGCACAGCGGATCGATTTTCCAGGTGCGGAGTTCACTC CCGTTGGAGGCCATTGGCTGGCCTTTGCGCACTGCGGATCGATTTTCCAGGTGCGGAGTTCACTC T A ATP7B Ensembl:ENSG00000123191 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:52011987..52012063 26863196 MeRIP-seq:(Medium) rs1254758817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276638,Human_RBP_ID_18641903 Human_Splice_Rec_1467841 105686 RMVar_ID_105686 Human_SNP_ID_530727971 m1A Human chr13 - 52028410 52028409 52028410 TCTTCTTCACTCTCAGCCAGAAAGCCAGTTATATCTCCTTCGTGAGGAACCACAATGTCAAGCTT TCTTCTTCACTCTCAGCCAGAAAGCCAGTTAT_TCTCCTTCGTGAGGAACCACAATGTCAAGCTT AT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:52028292..52028475 26863196 MeRIP-seq:(Medium) rs1420974704 Functional Loss DEL dbSNP153 33..33 33 - - - 105687 RMVar_ID_105687 Human_SNP_ID_530760070 m1A Human chr13 - 52159465 52159465 52159465 CGGCGCGTGGTCGCGGCGCGGAGCCGAGTGGGAGCGAGGGGTAGACGCGCCCCGGACGCGCGGCC CGGCGCGTGGTCGCGGCGCGGAGCCGAGTGGGGGCGAGGGGTAGACGCGCCCCGGACGCGCGGCC T C NEK3 Ensembl:ENSG00000136098 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:52159464..52159576 26863196 MeRIP-seq:(Medium) rs1475043582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3439503 105688 RMVar_ID_105688 Human_SNP_ID_530829727 m1A Human chr13 - 52450533 52450533 52450533 CCTGGAGATCAACGAGACCCTGGTGATCCAGCAGCGCGGGGTGCGAATCTACGATGGCGAGGAGA CCTGGAGATCAACGAGACCCTGGTGATCCAGCTGCGCGGGGTGCGAATCTACGATGGCGAGGAGA T A VPS36 Ensembl:ENSG00000136100 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:52450488..52450629 26863196 MeRIP-seq:(Medium) rs1167635526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_437879,Human_RBP_ID_812145,Human_RBP_ID_4276639,Human_RBP_ID_9367963,Human_RBP_ID_18417732,Human_RBP_ID_22919832 Human_Splice_Rec_1468605,Human_Splice_Rec_1468633,Human_Splice_Rec_1468679 Human_miRNA_ID_2000381 RMVar_hsa_circ_92895,RMVar_hsa_circ_163539 105689 RMVar_ID_105689 Human_SNP_ID_530863935 m1A Human chr13 + 52599603 52599603 52599603 GGGTAGTTAACGGGTTAATTCAGGTTATGTGTAGCTCTAGCTGGGAGAAGAAACAGGGCTTGGAG GGGTAGTTAACGGGTTAATTCAGGTTATGTGTGGCTCTAGCTGGGAGAAGAAACAGGGCTTGGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:52599580..52599711 26863196 MeRIP-seq:(Medium) rs1566146049 Functional Loss SNV dbSNP153 33..33 33 - - - 105690 RMVar_ID_105690 Human_SNP_ID_530873789 m1A Human chr13 - 52643125 52643125 52643125 AAGTTTCCTCCACGACCAAAGTTGTCATTCCCACCGAAACCATCTCCACGACCACCACCAAAGTT AAGTTTCCTCCACGACCAAAGTTGTCATTCCCGCCGAAACCATCTCCACGACCACCACCAAAGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:52643041..52643224 26863196 MeRIP-seq:(Medium) rs772450204 Functional Loss SNV dbSNP153 33..33 33 - - - 105691 RMVar_ID_105691 Human_SNP_ID_530875960 m1A Human chr13 - 52652216 52652216 52652216 GTACTATTCACTTCCCCAGAACGCCACAGCCCAGGCTTTCTTCTTAGTGGGCTTCCCAGACCAAG GTACTATTCACTTCCCCAGAACGCCACAGCCCGGGCTTTCTTCTTAGTGGGCTTCCCAGACCAAG T C AL139089.1 Ensembl:ENSG00000273723 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:52652175..52652287 26863196 MeRIP-seq:(Medium) rs1256982563 Functional Loss SNV dbSNP153 33..33 33 - - - 105692 RMVar_ID_105692 Human_SNP_ID_531977366 m1A Human chr13 + 57159463 57159463 57159463 CTCAGCCCCCCCCCCCCCCCCCCCCCCCCCCCAAGTAGCCGCAGCGAGCCGAGATGGCACCGCTG CTCAGCCCCCCCCCCCCCCCCCCCCCCCCCCCCAGTAGCCGCAGCGAGCCGAGATGGCACCGCTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:57159426..57159475 26863196 MeRIP-seq:(Medium) rs1458063283 Functional Loss SNV dbSNP153 33..33 33 - - - 105693 RMVar_ID_105693 Human_SNP_ID_532595556 m1A Human chr13 - 59702773 59702773 59702773 AGGGATTAACTAGGAGATTAGGTCAGAGAAGCAACAGGAGGCCAGACCATATAAAGCCTTGATAT AGGGATTAACTAGGAGATTAGGTCAGAGAAGCCACAGGAGGCCAGACCATATAAAGCCTTGATAT T G DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:59702768..59702906 26863196 MeRIP-seq:(Medium) rs1214176225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163585 105694 RMVar_ID_105694 Human_SNP_ID_532597581 m1A Human chr13 + 59711387 59711387 59711387 TACTACCACCATCCCCACAACTGTCATGATCAAGAACTATTTATCTCCATTTCTACCACACCATT TACTACCACCATCCCCACAACTGTCATGATCATGAACTATTTATCTCCATTTCTACCACACCATT A T lnc-TDRD3-11 RNACentral:URS00008B92AC lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:59711385..59711537 26863196 MeRIP-seq:(Medium) rs758295257 Functional Loss SNV dbSNP153 33..33 33 - - - 105695 RMVar_ID_105695 Human_SNP_ID_532623493 m1A Human chr13 + 59820976 59820976 59820976 CAACATATTATAATATCCTGTATATTTTTGCGACATAGAAAACTAGGAGATTTAATCATTTGAAA CAACATATTATAATATCCTGTATATTTTTGCGGCATAGAAAACTAGGAGATTTAATCATTTGAAA A G lnc-TDRD3-11 RNACentral:URS00008B92AC lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:59820925..59821057 26863196 MeRIP-seq:(Medium) rs1247913254 Functional Loss SNV dbSNP153 33..33 33 - - - 105696 RMVar_ID_105696 Human_SNP_ID_532643252 m1A Human chr13 - 59901315 59901307 59901316 GAGTTTGGCTATGTGAGGCCAGTGGCTGTGGCAGAGTGAAGGTGGGAGACGGTGTAAAGAGGCCA GAGTTTGGCTATGTGAGGCCAGTGGCTGTGG_________GGTGGGAGACGGTGTAAAGAGGCCA CTTCACTCTG C DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:59901301..59901391 26863196 MeRIP-seq:(Medium) rs375816578 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_8213,RMVar_hsa_circ_6237,RMVar_hsa_circ_89503,RMVar_hsa_circ_41657,RMVar_hsa_circ_79097,RMVar_hsa_circ_60639,RMVar_hsa_circ_163588,RMVar_hsa_circ_163587,RMVar_hsa_circ_306963,RMVar_hsa_circ_118318,RMVar_hsa_circ_51748,RMVar_hsa_circ_366122,RMVar_hsa_circ_348317,RMVar_hsa_circ_163593,RMVar_hsa_circ_163594,RMVar_hsa_circ_327971,RMVar_hsa_circ_339386,RMVar_hsa_circ_342712,RMVar_hsa_circ_70153,RMVar_hsa_circ_163595,RMVar_hsa_circ_163596,RMVar_hsa_circ_351556,RMVar_hsa_circ_357657,RMVar_hsa_circ_74662 105697 RMVar_ID_105697 Human_SNP_ID_154594770 m1A Human chr3 - 135965792 135965792 135965792 GCGGCTCAGCTCGCGGGCAGCGCTTGCCTCCAAGCCTCCCCGCGGCGCGGACTCTCGGGCTACGA GCGGCTCAGCTCGCGGGCAGCGCTTGCCTCCAGGCCTCCCCGCGGCGCGGACTCTCGGGCTACGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:135965683..135965837 26863196 MeRIP-seq:(Medium) rs1174216351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221525,RMVar_hsa_circ_221526 105698 RMVar_ID_105698 Human_SNP_ID_154594869 m1A Human chr3 - 135966045 135966036 135966046 GCCGGCCGCGCCGAGGCAACGCACCGCACCGCACCGCACCGACTGGAATTCCGACTTCCACAGCC GCCGGCCGCGCCGAGGCAACGCACCGCACCG__________ACTGGAATTCCGACTTCCACAGCC TCGGTGCGGTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:135966044..135966163 26863196 MeRIP-seq:(Medium) rs761032303 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_221525,RMVar_hsa_circ_221526 105699 RMVar_ID_105699 Human_SNP_ID_154594870 m1A Human chr3 - 135966045 135966036 135966046 GCCGGCCGCGCCGAGGCAACGCACCGCACCGCACCGCACCGACTGGAATTCCGACTTCCACAGCC GCCGGCCGCGCCGAGGCAACGCACCGCACCG_____CACCGACTGGAATTCCGACTTCCACAGCC TCGGTGCGGTG TCGGTG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:135966044..135966163 26863196 MeRIP-seq:(Medium) rs761032303 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_221525,RMVar_hsa_circ_221526 105700 RMVar_ID_105700 Human_SNP_ID_154647623 m1A Human chr3 + 136172266 136172266 136172266 CCCTCTCTCCACCTCTCATCATACTCATACTCACTCCCCGACAACACATACACACATACAGTACC CCCTCTCTCCACCTCTCATCATACTCATACTCGCTCCCCGACAACACATACACACATACAGTACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:136172250..136172465 26863196 MeRIP-seq:(Medium) rs937347240 Functional Loss SNV dbSNP153 33..33 33 - - - 105701 RMVar_ID_105701 Human_SNP_ID_154647987 m1A Human chr3 - 136173542 136173542 136173542 GTGGAATTGGCAGATTTTTATAAACTACATGCAGGGAGAACAATTGGATATGGAATGGAGGTGAA GTGGAATTGGCAGATTTTTATAAACTACATGCGGGGAGAACAATTGGATATGGAATGGAGGTGAA T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136173539..136173682 26863196 MeRIP-seq:(Medium) rs529807766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14633381,Human_RBP_ID_23971482 105702 RMVar_ID_105702 Human_SNP_ID_154655472 m1A Human chr3 + 136195627 136195627 136195627 AGGGCGCGGAGGCGGCGGCGACGGCAAGGACGACGGTCGGGCAGCGGCTTCCCGGATCTAGTGCA AGGGCGCGGAGGCGGCGGCGACGGCAAGGACGGCGGTCGGGCAGCGGCTTCCCGGATCTAGTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136195312..136195752 26863196 MeRIP-seq:(Medium) rs1291762243 Functional Loss SNV dbSNP153 33..33 33 - - - 105703 RMVar_ID_105703 Human_SNP_ID_154655717 m1A Human chr3 - 136196043 136196043 136196043 GCGGTGTGAGCGCTTGCCTTCCGCGGCCGGGGAGTGCTGAGGGCGGCGGCGGCCGTCGTGCTCGG GCGGTGTGAGCGCTTGCCTTCCGCGGCCGGGGGGTGCTGAGGGCGGCGGCGGCCGTCGTGCTCGG T C MSL2 Ensembl:ENSG00000174579 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:136196025..136196325 26863196 MeRIP-seq:(Medium) rs1329678162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758407,Human_RBP_ID_8236096,Human_RBP_ID_9333890,Human_RBP_ID_22093140 105704 RMVar_ID_105704 Human_SNP_ID_154655813 m1A Human chr3 + 136196255 136196255 136196255 GGCGCCTCAGGCCTCTGCTGGCGGCGACGACGACCGTTACCCCAACGGGCAAAGCCACTGTCATC GGCGCCTCAGGCCTCTGCTGGCGGCGACGACGTCCGTTACCCCAACGGGCAAAGCCACTGTCATC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136195838..136196572 26863196 MeRIP-seq:(Medium) rs1247279238 Functional Loss SNV dbSNP153 33..33 33 - - - 105705 RMVar_ID_105705 Human_SNP_ID_154655826 m1A Human chr3 + 136196285 136196285 136196285 CGACCGTTACCCCAACGGGCAAAGCCACTGTCATCCCCGAGACTCCCCCGCCGCCGTCGTCGCTA CGACCGTTACCCCAACGGGCAAAGCCACTGTCGTCCCCGAGACTCCCCCGCCGCCGTCGTCGCTA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:136196001..136196300 26863196 MeRIP-seq:(Medium) rs1232594336 Functional Loss SNV dbSNP153 33..33 33 - - - 105706 RMVar_ID_105706 Human_SNP_ID_154670048 m1A Human chr3 + 136250530 136250530 136250530 CAAGCGCCGGACCGCGCTGCTGGGAGGGGGCCAACGCCGTATTGACGCGCAGCACAAGCGAGTGA CAAGCGCCGGACCGCGCTGCTGGGAGGGGGCCGACGCCGTATTGACGCGCAGCACAAGCGAGTGA A G PCCB Ensembl:ENSG00000114054 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:136250405..136251289 32194978 MeRIP-seq:(Medium) rs769039164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248165,Human_RBP_ID_784354,Human_RBP_ID_1310017,Human_RBP_ID_5393640,Human_RBP_ID_22426534 Human_Splice_Rec_486961,Human_Splice_Rec_486989,Human_Splice_Rec_487013,Human_Splice_Rec_487039,Human_Splice_Rec_487067,Human_Splice_Rec_487093,Human_Splice_Rec_487123,Human_Splice_Rec_487169,Human_Splice_Rec_487199,Human_Splice_Rec_487229,Human_Splice_Rec_487239,Human_Splice_Rec_487255 105707 RMVar_ID_105707 Human_SNP_ID_154671813 m1A Human chr3 + 136255807 136255807 136255807 AAGCCCTCCCATGAACAGCCCTTGCTTTGCTTACTAAATTGTCTGTGATGACATCACTGAGTGAT AAGCCCTCCCATGAACAGCCCTTGCTTTGCTTGCTAAATTGTCTGTGATGACATCACTGAGTGAT A G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:136255798..136255870 26863196 MeRIP-seq:(Medium) rs770122436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22676687 105708 RMVar_ID_105708 Human_SNP_ID_154671814 m1A Human chr3 + 136255807 136255807 136255807 AAGCCCTCCCATGAACAGCCCTTGCTTTGCTTACTAAATTGTCTGTGATGACATCACTGAGTGAT AAGCCCTCCCATGAACAGCCCTTGCTTTGCTTTCTAAATTGTCTGTGATGACATCACTGAGTGAT A T PCCB Ensembl:ENSG00000114054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:136255798..136255870 26863196 MeRIP-seq:(Medium) rs770122436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22676687 105709 RMVar_ID_105709 Human_SNP_ID_154691684 m1A Human chr3 + 136326890 136326890 136326890 TGCATTCAATATTCCACTCATCACTTTTGTTGATGTCCCTGGCTTTCTACCTGGTAAGTTTTTGA TGCATTCAATATTCCACTCATCACTTTTGTTGTTGTCCCTGGCTTTCTACCTGGTAAGTTTTTGA A T PCCB Ensembl:ENSG00000114054 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:136317050..136326928 32194978 MeRIP-seq:(Medium) rs1448763626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_590216,Human_RBP_ID_22092512,Human_RBP_ID_22455586 Human_Splice_Rec_486980,Human_Splice_Rec_486981,Human_Splice_Rec_487004,Human_Splice_Rec_487005,Human_Splice_Rec_487030,Human_Splice_Rec_487031,Human_Splice_Rec_487058,Human_Splice_Rec_487059,Human_Splice_Rec_487084,Human_Splice_Rec_487085,Human_Splice_Rec_487114,Human_Splice_Rec_487115,Human_Splice_Rec_487142,Human_Splice_Rec_487143,Human_Splice_Rec_487160,Human_Splice_Rec_487161,Human_Splice_Rec_487188,Human_Splice_Rec_487189,Human_Splice_Rec_487220,Human_Splice_Rec_487221,Human_Splice_Rec_487266,Human_Splice_Rec_487267,Human_Splice_Rec_487316,Human_Splice_Rec_487340 RMVar_hsa_circ_25215,RMVar_hsa_circ_100419,RMVar_hsa_circ_77693,RMVar_hsa_circ_221539,RMVar_hsa_circ_221545,RMVar_hsa_circ_376375,RMVar_hsa_circ_221550,RMVar_hsa_circ_221549,RMVar_hsa_circ_116516,RMVar_hsa_circ_267536,RMVar_hsa_circ_221555,RMVar_hsa_circ_221557,RMVar_hsa_circ_273380,RMVar_hsa_circ_377426,RMVar_hsa_circ_271567,RMVar_hsa_circ_221556,RMVar_hsa_circ_221558,RMVar_hsa_circ_283798,RMVar_hsa_circ_298744,RMVar_hsa_circ_221559 105710 RMVar_ID_105710 Human_SNP_ID_154692651 m1A Human chr3 + 136329976 136329976 136329976 CCCGAATCTGCTGTGACCTGGATGTCTTGGCCAGCAAGAAGGTACAACGTCCTTGGAGAAAACAT CCCGAATCTGCTGTGACCTGGATGTCTTGGCCGGCAAGAAGGTACAACGTCCTTGGAGAAAACAT A G PCCB Ensembl:ENSG00000114054 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:136329926..136330077 32194978 MeRIP-seq:(Medium) rs1560035695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_590222,Human_RBP_ID_3965505,Human_RBP_ID_17661582,Human_RBP_ID_22455588 Human_Splice_Rec_486988,Human_Splice_Rec_487012,Human_Splice_Rec_487038,Human_Splice_Rec_487066,Human_Splice_Rec_487092,Human_Splice_Rec_487122,Human_Splice_Rec_487148,Human_Splice_Rec_487168,Human_Splice_Rec_487196,Human_Splice_Rec_487197,Human_Splice_Rec_487228,Human_Splice_Rec_487346 Human_miRNA_ID_2477298 Clinvar_Rec_678 RMVar_hsa_circ_77693,RMVar_hsa_circ_221545,RMVar_hsa_circ_221550,RMVar_hsa_circ_116516,RMVar_hsa_circ_98170,RMVar_hsa_circ_221557,RMVar_hsa_circ_273380,RMVar_hsa_circ_377426,RMVar_hsa_circ_221556,RMVar_hsa_circ_221558,RMVar_hsa_circ_283798,RMVar_hsa_circ_95374,RMVar_hsa_circ_221560,RMVar_hsa_circ_221561 105711 RMVar_ID_105711 Human_SNP_ID_154721081 m1A Human chr3 + 136434738 136434738 136434738 TTGTATTGCCTTCAAAGATCTCTCTGTCCTGCAGATTACACTAATATGTTCTTCATTTTCTTCTA TTGTATTGCCTTCAAAGATCTCTCTGTCCTGCGGATTACACTAATATGTTCTTCATTTTCTTCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136434736..136434849 26863196 MeRIP-seq:(Medium) rs1230218048 Functional Loss SNV dbSNP153 33..33 33 - - - 105712 RMVar_ID_105712 Human_SNP_ID_154774690 m1A Human chr3 + 136618101 136618101 136618101 AGTATGTTCAATTCTTTGCCTTCTACTTTTAAACTTAACTTCCTCATAAAGCAACCTTTTCCAAT AGTATGTTCAATTCTTTGCCTTCTACTTTTAACCTTAACTTCCTCATAAAGCAACCTTTTCCAAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136618095..136618182 26863196 MeRIP-seq:(Medium) rs1026369727 Functional Loss SNV dbSNP153 33..33 33 - - - 105713 RMVar_ID_105713 Human_SNP_ID_154782079 m1A Human chr3 + 136646036 136646036 136646036 TCCACAGCCCGACACTTTAACCAATATGACCTAATCTTCCAACATTCACAGCTTTCTCATGCTTA TCCACAGCCCGACACTTTAACCAATATGACCTCATCTTCCAACATTCACAGCTTTCTCATGCTTA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136646031..136646147 26863196 MeRIP-seq:(Medium) rs1424854835 Functional Loss SNV dbSNP153 33..33 33 - - - 105714 RMVar_ID_105714 Human_SNP_ID_154806795 m1A Human chr3 + 136734980 136734980 136734980 CACAGTGAACTCGTCCTCTCCACCAGGCCTGCAGTTTCTGGTCAGAACTCTTGACACTAACCTAG CACAGTGAACTCGTCCTCTCCACCAGGCCTGCGGTTTCTGGTCAGAACTCTTGACACTAACCTAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:136734977..136735127 26863196 MeRIP-seq:(Medium) rs1245517137 Functional Loss SNV dbSNP153 33..33 33 - - - 105715 RMVar_ID_105715 Human_SNP_ID_154811746 m1A Human chr3 - 136752175 136752166 136752175 ATGGGCAGCTGAGGTGAGTGCGGGCGGCGGCGACGGCGGCGGGGGGCGGGAAAGAGGGGGAATGC ATGGGCAGCTGAGGTGAGTGCGGGCGGCGGCG_________GGGGGCGGGAAAGAGGGGGAATGC CCGCCGCCGT C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:136752152..136752370 26863196 MeRIP-seq:(Medium) rs995861141 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_9333892,Human_RBP_ID_18953869 RMVar_hsa_circ_47258 105716 RMVar_ID_105716 Human_SNP_ID_154811751 m1A Human chr3 - 136752175 136752175 136752175 ATGGGCAGCTGAGGTGAGTGCGGGCGGCGGCGACGGCGGCGGGGGGCGGGAAAGAGGGGGAATGC ATGGGCAGCTGAGGTGAGTGCGGGCGGCGGCGGCGGCGGCGGGGGGCGGGAAAGAGGGGGAATGC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:136752152..136752370 26863196 MeRIP-seq:(Medium) rs1559991179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9333892,Human_RBP_ID_18953869 RMVar_hsa_circ_47258 105717 RMVar_ID_105717 Human_SNP_ID_154833392 m1A Human chr3 - 136839917 136839917 136839917 AGTCTGGGTTATAGAAGTGGGTGGAAATTACAACTAAGGGACTTGGAGATGAGGGGAGGTAAGAA AGTCTGGGTTATAGAAGTGGGTGGAAATTACAGCTAAGGGACTTGGAGATGAGGGGAGGTAAGAA T C NCK1-DT Ensembl:ENSG00000239213 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:136839867..136839943 26863196 MeRIP-seq:(Medium) rs1569228 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14259,GWAS_ID_14260,GWAS_ID_14261,GWAS_ID_14262,GWAS_ID_14263,GWAS_ID_14264,GWAS_ID_14265,GWAS_ID_14266,GWAS_ID_14267,GWAS_ID_14268,GWAS_ID_14269,GWAS_ID_14270,GWAS_ID_14271,GWAS_ID_14272,GWAS_ID_14273,GWAS_ID_14274,GWAS_ID_14275,GWAS_ID_14276,GWAS_ID_14277,GWAS_ID_14278,GWAS_ID_14279,GWAS_ID_14280,GWAS_ID_14281,GWAS_ID_14282,GWAS_ID_14283,GWAS_ID_14284,GWAS_ID_14285,GWAS_ID_14286,GWAS_ID_14287,GWAS_ID_14288,GWAS_ID_14289,GWAS_ID_14290,GWAS_ID_14291,GWAS_ID_14292,GWAS_ID_14293,GWAS_ID_14294,GWAS_ID_14295,GWAS_ID_14296,GWAS_ID_14297,GWAS_ID_14298,GWAS_ID_14299,GWAS_ID_14300,GWAS_ID_14301,GWAS_ID_14302,GWAS_ID_14303,GWAS_ID_14304,GWAS_ID_14305,GWAS_ID_14306,GWAS_ID_14307,GWAS_ID_14308,GWAS_ID_14309,GWAS_ID_14310,GWAS_ID_14311,GWAS_ID_14312,GWAS_ID_14313,GWAS_ID_14314,GWAS_ID_14315,GWAS_ID_14316,GWAS_ID_14317,GWAS_ID_14318,GWAS_ID_14319,GWAS_ID_14320,GWAS_ID_14321,GWAS_ID_14322,GWAS_ID_14323,GWAS_ID_14324,GWAS_ID_14325,GWAS_ID_14326,GWAS_ID_14327,GWAS_ID_14328,GWAS_ID_14329,GWAS_ID_14330,GWAS_ID_14331,GWAS_ID_14332,GWAS_ID_14333,GWAS_ID_14334,GWAS_ID_14335,GWAS_ID_14336,GWAS_ID_14337,GWAS_ID_14338,GWAS_ID_14339,GWAS_ID_14340,GWAS_ID_14341,GWAS_ID_14342,GWAS_ID_14343,GWAS_ID_14344,GWAS_ID_14345,GWAS_ID_14346,GWAS_ID_14347,GWAS_ID_14348,GWAS_ID_14349,GWAS_ID_14350,GWAS_ID_14351,GWAS_ID_14352,GWAS_ID_14353,GWAS_ID_14354,GWAS_ID_14355,GWAS_ID_14356,GWAS_ID_14357,GWAS_ID_14358,GWAS_ID_14359,GWAS_ID_14360,GWAS_ID_14361,GWAS_ID_14362,GWAS_ID_14363,GWAS_ID_14364,GWAS_ID_14365,GWAS_ID_14366,GWAS_ID_14367,GWAS_ID_14368,GWAS_ID_14369,GWAS_ID_14370,GWAS_ID_14371,GWAS_ID_14372,GWAS_ID_14373,GWAS_ID_14374,GWAS_ID_14375,GWAS_ID_14376,GWAS_ID_14377,GWAS_ID_14378,GWAS_ID_14379,GWAS_ID_14380,GWAS_ID_14381,GWAS_ID_14382,GWAS_ID_14383,GWAS_ID_14384,GWAS_ID_14385,GWAS_ID_14386,GWAS_ID_14387,GWAS_ID_14388,GWAS_ID_14389,GWAS_ID_14390,GWAS_ID_14391,GWAS_ID_14392,GWAS_ID_14393,GWAS_ID_14394,GWAS_ID_14395,GWAS_ID_14396,GWAS_ID_14397,GWAS_ID_14398,GWAS_ID_14399,GWAS_ID_14400,GWAS_ID_14401,GWAS_ID_14402,GWAS_ID_14403,GWAS_ID_14404,GWAS_ID_14405,GWAS_ID_14406,GWAS_ID_14407,GWAS_ID_14408,GWAS_ID_14409,GWAS_ID_14410,GWAS_ID_14411,GWAS_ID_14412,GWAS_ID_14413,GWAS_ID_14414,GWAS_ID_14415,GWAS_ID_14416,GWAS_ID_14417,GWAS_ID_14418,GWAS_ID_14419,GWAS_ID_14420,GWAS_ID_14421,GWAS_ID_14422,GWAS_ID_14423,GWAS_ID_14424,GWAS_ID_14425,GWAS_ID_14426,GWAS_ID_14427,GWAS_ID_14428,GWAS_ID_14429,GWAS_ID_14430,GWAS_ID_14431,GWAS_ID_14432,GWAS_ID_14433,GWAS_ID_14434,GWAS_ID_14435,GWAS_ID_14436,GWAS_ID_14437,GWAS_ID_14438,GWAS_ID_14439,GWAS_ID_14440,GWAS_ID_14441,GWAS_ID_14442,GWAS_ID_14443,GWAS_ID_14444,GWAS_ID_14445,GWAS_ID_14446,GWAS_ID_14447,GWAS_ID_14448,GWAS_ID_14449,GWAS_ID_14450,GWAS_ID_14451,GWAS_ID_14452,GWAS_ID_14453,GWAS_ID_14454,GWAS_ID_14455,GWAS_ID_14456,GWAS_ID_14457,GWAS_ID_14458,GWAS_ID_14459,GWAS_ID_14460,GWAS_ID_14461,GWAS_ID_14462,GWAS_ID_14463,GWAS_ID_14464,GWAS_ID_14465,GWAS_ID_14466,GWAS_ID_14467,GWAS_ID_14468,GWAS_ID_14469,GWAS_ID_14470,GWAS_ID_14471,GWAS_ID_14472,GWAS_ID_14473,GWAS_ID_14474,GWAS_ID_14475,GWAS_ID_14476,GWAS_ID_14477,GWAS_ID_14478,GWAS_ID_14479,GWAS_ID_14480,GWAS_ID_14481,GWAS_ID_14482,GWAS_ID_14483,GWAS_ID_14484,GWAS_ID_14485,GWAS_ID_14486,GWAS_ID_14487,GWAS_ID_14488,GWAS_ID_14489,GWAS_ID_14490,GWAS_ID_14491,GWAS_ID_14492,GWAS_ID_14493,GWAS_ID_14494,GWAS_ID_14495,GWAS_ID_14496,GWAS_ID_14497,GWAS_ID_14498,GWAS_ID_14499,GWAS_ID_14500,GWAS_ID_14501,GWAS_ID_14502,GWAS_ID_14503,GWAS_ID_14504,GWAS_ID_14505,GWAS_ID_14506,GWAS_ID_14507,GWAS_ID_14508,GWAS_ID_14509,GWAS_ID_14510,GWAS_ID_14511,GWAS_ID_14512,GWAS_ID_14513,GWAS_ID_14514,GWAS_ID_14515,GWAS_ID_14516,GWAS_ID_14517,GWAS_ID_14518,GWAS_ID_14519,GWAS_ID_14520,GWAS_ID_14521,GWAS_ID_14522,GWAS_ID_14523,GWAS_ID_14524,GWAS_ID_14525,GWAS_ID_14526,GWAS_ID_14527,GWAS_ID_14528,GWAS_ID_14529,GWAS_ID_14530,GWAS_ID_14531,GWAS_ID_14532 105718 RMVar_ID_105718 Human_SNP_ID_154833397 m1A Human chr3 + 136839945 136839945 136839945 TTAGTTGTAATTTCCACCCACTTCTATAACCCAGACTGACACAGCCCAGCAAAATCCTCAGGTCT TTAGTTGTAATTTCCACCCACTTCTATAACCCGGACTGACACAGCCCAGCAAAATCCTCAGGTCT A G SLC35G2 Ensembl:ENSG00000168917 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136839768..136840067 26863196 MeRIP-seq:(Medium) rs1007677581 Functional Loss SNV dbSNP153 33..33 33 - - - 105719 RMVar_ID_105719 Human_SNP_ID_154833505 m1A Human chr3 - 136840474 136840472 136840475 GGGGAGGAAGAGGAGGAGGAAGAAAGAAAAGAAGGGCAACAACCAGGGGAAGAATATGGATGAAT GGGGAGGAAGAGGAGGAGGAAGAAAGAAAAG___GGCAACAACCAGGGGAAGAATATGGATGAAT CCTT C NCK1-DT Ensembl:ENSG00000239213 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136840385..136840649 26863196 MeRIP-seq:(Medium) rs1299465366 Functional Loss DEL dbSNP153 32..34 33 - - - 105720 RMVar_ID_105720 Human_SNP_ID_154833542 m1A Human chr3 - 136840539 136840539 136840539 GGAAAAGAGAGAAAAAGAGAAGGAAGGGAGAGAGGGAGGGAGGGAGAGAGAGAGGAAGGGAGGGA GGAAAAGAGAGAAAAAGAGAAGGAAGGGAGAGGGGGAGGGAGGGAGAGAGAGAGGAAGGGAGGGA T C NCK1-DT Ensembl:ENSG00000239213 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:136840492..136840582 26863196 MeRIP-seq:(Medium) rs375100954 Functional Loss SNV dbSNP153 33..33 33 - - - 105721 RMVar_ID_105721 Human_SNP_ID_154833543 m1A Human chr3 - 136840539 136840539 136840539 GGAAAAGAGAGAAAAAGAGAAGGAAGGGAGAGAGGGAGGGAGGGAGAGAGAGAGGAAGGGAGGGA GGAAAAGAGAGAAAAAGAGAAGGAAGGGAGAGCGGGAGGGAGGGAGAGAGAGAGGAAGGGAGGGA T G NCK1-DT Ensembl:ENSG00000239213 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:136840492..136840582 26863196 MeRIP-seq:(Medium) rs375100954 Functional Loss SNV dbSNP153 33..33 33 - - - 105722 RMVar_ID_105722 Human_SNP_ID_154838857 m1A Human chr3 - 136861990 136861990 136861990 GCTAGAGGGTGAGAAGCGCTGGGCCGGACCAGAACTGTCTTAGCTTTTCCCTCTGCGGCTGCTCT GCTAGAGGGTGAGAAGCGCTGGGCCGGACCAGGACTGTCTTAGCTTTTCCCTCTGCGGCTGCTCT T C NCK1-DT Ensembl:ENSG00000239213 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:136861836..136862036 26863196 MeRIP-seq:(Medium) rs545451911 Functional Loss SNV dbSNP153 33..33 33 - - - 105723 RMVar_ID_105723 Human_SNP_ID_154838858 m1A Human chr3 - 136861992 136861992 136861992 GAGCTAGAGGGTGAGAAGCGCTGGGCCGGACCAGAACTGTCTTAGCTTTTCCCTCTGCGGCTGCT GAGCTAGAGGGTGAGAAGCGCTGGGCCGGACCGGAACTGTCTTAGCTTTTCCCTCTGCGGCTGCT T C NCK1-DT Ensembl:ENSG00000239213 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136861921..136862019 26863196 MeRIP-seq:(Medium) rs565367397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5604540 105724 RMVar_ID_105724 Human_SNP_ID_154839003 m1A Human chr3 - 136862313 136862310 136862313 TGCCGAGCCGGGCAGCTCCAGCTCACCTGAGGAGGGCTCCAGGACGCCACTGCGGCCGCCGTGAT TGCCGAGCCGGGCAGCTCCAGCTCACCTGAGG___GCTCCAGGACGCCACTGCGGCCGCCGTGAT CCCT C NCK1-DT Ensembl:ENSG00000239213 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:136862281..136862432 26863196 MeRIP-seq:(Medium) rs1004502039 Functional Loss DEL dbSNP153 33..35 33 - - - 105725 RMVar_ID_105725 Human_SNP_ID_154866951 m1A Human chr3 - 136975875 136975875 136975875 TACCACTGCCAGCATCCAAGCAAGCCATGTGGAGGCCCAATGATCAGCATTCTGGTAACCACCAA TACCACTGCCAGCATCCAAGCAAGCCATGTGGTGGCCCAATGATCAGCATTCTGGTAACCACCAA T A IL20RB-AS1 Ensembl:ENSG00000249407 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136975756..136975942 26863196 MeRIP-seq:(Medium) rs1435785958 Functional Loss SNV dbSNP153 33..33 33 - - - 105726 RMVar_ID_105726 Human_SNP_ID_154868913 m1A Human chr3 + 136984447 136984447 136984447 GCAAGGAATGGGTGGGAATGTAACCAGTTTAGAGCTGCAGGAAAGGCAAGATAAGGGTCTTCTTT GCAAGGAATGGGTGGGAATGTAACCAGTTTAGCGCTGCAGGAAAGGCAAGATAAGGGTCTTCTTT A C IL20RB Ensembl:ENSG00000174564 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:136984426..136984509 26863196 MeRIP-seq:(Medium) rs1384653064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15443,RMVar_hsa_circ_101899,RMVar_hsa_circ_315361,RMVar_hsa_circ_221620,RMVar_hsa_circ_301405,RMVar_hsa_circ_366047,RMVar_hsa_circ_221619,RMVar_hsa_circ_76501,RMVar_hsa_circ_221622 105727 RMVar_ID_105727 Human_SNP_ID_155118169 m1A Human chr3 - 138012442 138012442 138012442 GGGGAGTAAGAGACTGCCAAGGAAGGTAGGTGAGGGGTTAGGAAGGCTTGGTGTCAGGCTGTTAT GGGGAGTAAGAGACTGCCAAGGAAGGTAGGTGGGGGGTTAGGAAGGCTTGGTGTCAGGCTGTTAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138012391..138012548 26863196 MeRIP-seq:(Medium) rs1051352964 Functional Loss SNV dbSNP153 33..33 33 - - - 105728 RMVar_ID_105728 Human_SNP_ID_155118175 m1A Human chr3 + 138012468 138012468 138012468 AACCCCTCACCTACCTTCCTTGGCAGTCTCTTACTCCCCCATCCTGTTTCTTCTGTCCTTTCAGT AACCCCTCACCTACCTTCCTTGGCAGTCTCTTTCTCCCCCATCCTGTTTCTTCTGTCCTTTCAGT A T CLDN18 Ensembl:ENSG00000066405 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138012417..138012511 26863196 MeRIP-seq:(Medium) rs1208971403 Functional Loss SNV dbSNP153 33..33 33 - - - 105729 RMVar_ID_105729 Human_SNP_ID_155119634 m1A Human chr3 + 138019467 138019467 138019467 ATGCCTGAAGGTATGGCTCCTCCCATCCGCCTACTCCACCAGGGCCCCAGTCCAGGCCTTTGGCT ATGCCTGAAGGTATGGCTCCTCCCATCCGCCTGCTCCACCAGGGCCCCAGTCCAGGCCTTTGGCT A G CLDN18 Ensembl:ENSG00000066405 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:138019438..138019584 26863196 MeRIP-seq:(Medium) rs746511132 Functional Loss SNV dbSNP153 33..33 33 - - - 105730 RMVar_ID_105730 Human_SNP_ID_155125915 m1A Human chr3 + 138049785 138049785 138049785 CACACCTCATCCCTCTCCTCTCTCAAGTCCAGACTACCATTTTCTGGCTTCTTCCAGGCCACCCT CACACCTCATCCCTCTCCTCTCTCAAGTCCAGCCTACCATTTTCTGGCTTCTTCCAGGCCACCCT A C lnc-CLDN18-1 RNACentral:URS00008B5193 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138049735..138049809 26863196 MeRIP-seq:(Medium) rs766992481 Functional Loss SNV dbSNP153 33..33 33 - - - 105731 RMVar_ID_105731 Human_SNP_ID_155126640 m1A Human chr3 - 138051283 138051281 138051284 CCACTACCACCATCACCACCTCTACCACCACCACAACCACCACCTCCACCACTACCACCTCCACC CCACTACCACCATCACCACCTCTACCACCAC___AACCACCACCTCCACCACTACCACCTCCACC TGTG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:138051200..138051301 26863196 MeRIP-seq:(Medium) rs1464045241 Functional Loss DEL dbSNP153 32..34 33 - - - 105732 RMVar_ID_105732 Human_SNP_ID_155126642 m1A Human chr3 - 138051283 138051283 138051283 CCACTACCACCATCACCACCTCTACCACCACCACAACCACCACCTCCACCACTACCACCTCCACC CCACTACCACCATCACCACCTCTACCACCACCTCAACCACCACCTCCACCACTACCACCTCCACC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:138051200..138051301 26863196 MeRIP-seq:(Medium) rs1213317601 Functional Loss SNV dbSNP153 33..33 33 - - - 105733 RMVar_ID_105733 Human_SNP_ID_155130621 m1A Human chr3 - 138068253 138068253 138068253 GGCAGAGCCACCCCCACCAACTCGTCAGAGCCATGGCAGCCATGGCTCCAGCCTGACCCAGGTGT GGCAGAGCCACCCCCACCAACTCGTCAGAGCCGTGGCAGCCATGGCTCCAGCCTGACCCAGGTGT T C DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138068202..138068273 26863196 MeRIP-seq:(Medium) rs779404923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38150,RMVar_hsa_circ_336604,RMVar_hsa_circ_351330,RMVar_hsa_circ_335302 105734 RMVar_ID_105734 Human_SNP_ID_155134959 m1A Human chr3 - 138087025 138087025 138087025 AGGGCCCATTTGATAAGCTTTTAATCTTTTTCAGAAAACGGAGTGGAAAAGAAAAGTGAAGGAAC AGGGCCCATTTGATAAGCTTTTAATCTTTTTCCGAAAACGGAGTGGAAAAGAAAAGTGAAGGAAC T G DZIP1L Ensembl:ENSG00000158163 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138086976..138087025 26863196 MeRIP-seq:(Medium) rs763324082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_488093,Human_Splice_Rec_488117,Human_Splice_Rec_488139 RMVar_hsa_circ_351330,RMVar_hsa_circ_335302,RMVar_hsa_circ_59182,RMVar_hsa_circ_375024,RMVar_hsa_circ_59578,RMVar_hsa_circ_221629,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_58062 105735 RMVar_ID_105735 Human_SNP_ID_155138852 m1A Human chr3 - 138103511 138103511 138103511 CCGCCGGCGTCGCAAGATGATCAGCACCCTGCAGCAGCTGCTAATGCAGACAGGCACCCACAGCT CCGCCGGCGTCGCAAGATGATCAGCACCCTGCCGCAGCTGCTAATGCAGACAGGCACCCACAGCT T G DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:138103469..138103553 26863196 MeRIP-seq:(Medium) rs778668538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_488083,Human_Splice_Rec_488129,Human_Splice_Rec_488155 RMVar_hsa_circ_335302,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_61976 105736 RMVar_ID_105736 Human_SNP_ID_155139043 m1A Human chr3 - 138103938 138103929 138103938 TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTCAGTGGCCCCCTCTTTGGGGCCTACACGTTCCCC TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTC_________CTCTTTGGGGCCTACACGTTCCCC GGGGGCCACT G DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138103888..138104037 26863196 MeRIP-seq:(Medium) rs1224857476 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_335302,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_61976 105737 RMVar_ID_105737 Human_SNP_ID_155139049 m1A Human chr3 - 138103938 138103938 138103938 TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTCAGTGGCCCCCTCTTTGGGGCCTACACGTTCCCC TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTCGGTGGCCCCCTCTTTGGGGCCTACACGTTCCCC T C DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138103888..138104037 26863196 MeRIP-seq:(Medium) rs146109164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335302,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_61976 105738 RMVar_ID_105738 Human_SNP_ID_155139050 m1A Human chr3 - 138103938 138103938 138103938 TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTCAGTGGCCCCCTCTTTGGGGCCTACACGTTCCCC TGCAGTCCCCAGCTGCCACTGCTGAGGGCCTCCGTGGCCCCCTCTTTGGGGCCTACACGTTCCCC T G DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138103888..138104037 26863196 MeRIP-seq:(Medium) rs146109164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335302,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_61976 105739 RMVar_ID_105739 Human_SNP_ID_155141726 m1A Human chr3 - 138115405 138115405 138115405 CTGGGCTGTCTGGGGCGGTGGAGCAAGTCTGGAGGCGGGACGTGGGGCGAGTATGGGAGCCGCCA CTGGGCTGTCTGGGGCGGTGGAGCAAGTCTGGCGGCGGGACGTGGGGCGAGTATGGGAGCCGCCA T G DZIP1L Ensembl:ENSG00000158163 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:138115307..138115510 26863196 MeRIP-seq:(Medium) rs1217360687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_488081,Human_Splice_Rec_488165 RMVar_hsa_circ_102473,RMVar_hsa_circ_221628 105740 RMVar_ID_105740 Human_SNP_ID_155141786 m1A Human chr3 + 138115577 138115577 138115577 AGTGCCGCCAACCTGCGGGACCGCGGACAGAGAGCTCCTCGGTGCGTCGGTCAGCTCGTGGCTTG AGTGCCGCCAACCTGCGGGACCGCGGACAGAGGGCTCCTCGGTGCGTCGGTCAGCTCGTGGCTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138115368..138115625 26863196 MeRIP-seq:(Medium) rs908779812 Functional Loss SNV dbSNP153 33..33 33 - - - 105741 RMVar_ID_105741 Human_SNP_ID_155178648 m1A Human chr3 - 138265686 138265686 138265686 AGTCATAAAGGTATACTTGCCGTTCCCTACACATACCATACATAATGTTTCTCCTCATGCTATTC AGTCATAAAGGTATACTTGCCGTTCCCTACACGTACCATACATAATGTTTCTCCTCATGCTATTC T C NME9 Ensembl:ENSG00000181322 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138265636..138265708 26863196 MeRIP-seq:(Medium) rs1486150361 Functional Loss SNV dbSNP153 33..33 33 - - - 105742 RMVar_ID_105742 Human_SNP_ID_155203279 m1A Human chr3 + 138372849 138372848 138372850 CTAAGTTAAAAAAGCCCTCTGTCTCATTCCACATGTCTTGCTGCCGCAGGTCTGACCTACGAGAA CTAAGTTAAAAAAGCCCTCTGTCTCATTCCAC__GTCTTGCTGCCGCAGGTCTGACCTACGAGAA CAT C MRAS Ensembl:ENSG00000158186 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:138372843..138372928 26863410 MeRIP-seq:(Medium) rs1398301625 Functional Loss DEL dbSNP153 33..34 33 - - - 105743 RMVar_ID_105743 Human_SNP_ID_155203280 m1A Human chr3 + 138372849 138372849 138372849 CTAAGTTAAAAAAGCCCTCTGTCTCATTCCACATGTCTTGCTGCCGCAGGTCTGACCTACGAGAA CTAAGTTAAAAAAGCCCTCTGTCTCATTCCACGTGTCTTGCTGCCGCAGGTCTGACCTACGAGAA A G MRAS Ensembl:ENSG00000158186 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:138372843..138372928 26863410 MeRIP-seq:(Medium) rs1327745475 Functional Loss SNV dbSNP153 33..33 33 - - - 105744 RMVar_ID_105744 Human_SNP_ID_155206089 m1A Human chr3 - 138384991 138384991 138384991 ACTCTAATTAGACTTTCATCTCCAACCACTCCATCAAAACTGATCTTGTCAAGTCACCAATGACC ACTCTAATTAGACTTTCATCTCCAACCACTCCTTCAAAACTGATCTTGTCAAGTCACCAATGACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:138384948..138385073 26863196 MeRIP-seq:(Medium) rs986710196 Functional Loss SNV dbSNP153 33..33 33 - - - 105745 RMVar_ID_105745 Human_SNP_ID_155210334 m1A Human chr3 - 138403273 138403273 138403273 GTTACTTTGACGTGTCAGTGTATTCGTATCAGAGAGGCACCAAGCAGCACAGCTGATGTGAAAAC GTTACTTTGACGTGTCAGTGTATTCGTATCAGGGAGGCACCAAGCAGCACAGCTGATGTGAAAAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:138403146..138403297 32194978 MeRIP-seq:(Medium) rs1413604121 Functional Loss SNV dbSNP153 33..33 33 - - - 105746 RMVar_ID_105746 Human_SNP_ID_155217422 m1A Human chr3 - 138434652 138434652 138434652 TGCCCTGCTGGGACTCTCGGCGCGCCGAGCTCAGGGTTCTCTGCGACGGAGAGCAGCGCCTGGAA TGCCCTGCTGGGACTCTCGGCGCGCCGAGCTCCGGGTTCTCTGCGACGGAGAGCAGCGCCTGGAA T G HSALNG0029266 RNACentral:URS0000E9E167 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138434601..138434837 26863196 MeRIP-seq:(Medium) rs1400970799 Functional Loss SNV dbSNP153 33..33 33 - - - 105747 RMVar_ID_105747 Human_SNP_ID_155242498 m1A Human chr3 + 138535775 138535775 138535775 ACCCAGTCATCTTAACTGTTTTTTGTTTTTTCATTCTTCCCTTCCAATTTCTCTCTTCTTCTTCC ACCCAGTCATCTTAACTGTTTTTTGTTTTTTCTTTCTTCCCTTCCAATTTCTCTCTTCTTCTTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138535725..138535937 26863196 MeRIP-seq:(Medium) rs1344328385 Functional Loss SNV dbSNP153 33..33 33 - - - 105748 RMVar_ID_105748 Human_SNP_ID_155250774 m1A Human chr3 - 138570321 138570321 138570321 ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTACAGGTACTGAGTTATGAATTCTTAGATGATGG ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTTCAGGTACTGAGTTATGAATTCTTAGATGATGG T A CEP70 Ensembl:ENSG00000114107 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1673608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19118557,Human_RBP_ID_23018264 Human_Splice_Rec_489037,Human_Splice_Rec_489097,Human_Splice_Rec_489131,Human_Splice_Rec_489169,Human_Splice_Rec_489197,Human_Splice_Rec_489215,Human_Splice_Rec_489233,Human_Splice_Rec_489247 GWAS_ID_14533,GWAS_ID_14534,GWAS_ID_14535,GWAS_ID_14536,GWAS_ID_14537,GWAS_ID_14538 RMVar_hsa_circ_68372,RMVar_hsa_circ_38778,RMVar_hsa_circ_221679,RMVar_hsa_circ_13379,RMVar_hsa_circ_317158,RMVar_hsa_circ_270865,RMVar_hsa_circ_96880,RMVar_hsa_circ_221680,RMVar_hsa_circ_291358,RMVar_hsa_circ_221678,RMVar_hsa_circ_30245,RMVar_hsa_circ_221687,RMVar_hsa_circ_366269,RMVar_hsa_circ_221686,RMVar_hsa_circ_367399,RMVar_hsa_circ_348897,RMVar_hsa_circ_221691,RMVar_hsa_circ_273859,RMVar_hsa_circ_288279,RMVar_hsa_circ_221692,RMVar_hsa_circ_221689,RMVar_hsa_circ_221690,RMVar_hsa_circ_221688 105749 RMVar_ID_105749 Human_SNP_ID_155250775 m1A Human chr3 - 138570321 138570321 138570321 ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTACAGGTACTGAGTTATGAATTCTTAGATGATGG ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTGCAGGTACTGAGTTATGAATTCTTAGATGATGG T C CEP70 Ensembl:ENSG00000114107 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1673608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19118557,Human_RBP_ID_23018264 Human_Splice_Rec_489037,Human_Splice_Rec_489097,Human_Splice_Rec_489131,Human_Splice_Rec_489169,Human_Splice_Rec_489197,Human_Splice_Rec_489215,Human_Splice_Rec_489233,Human_Splice_Rec_489247 GWAS_ID_14533,GWAS_ID_14534,GWAS_ID_14535,GWAS_ID_14536,GWAS_ID_14537,GWAS_ID_14538 RMVar_hsa_circ_68372,RMVar_hsa_circ_38778,RMVar_hsa_circ_221679,RMVar_hsa_circ_13379,RMVar_hsa_circ_317158,RMVar_hsa_circ_270865,RMVar_hsa_circ_96880,RMVar_hsa_circ_221680,RMVar_hsa_circ_291358,RMVar_hsa_circ_221678,RMVar_hsa_circ_30245,RMVar_hsa_circ_221687,RMVar_hsa_circ_366269,RMVar_hsa_circ_221686,RMVar_hsa_circ_367399,RMVar_hsa_circ_348897,RMVar_hsa_circ_221691,RMVar_hsa_circ_273859,RMVar_hsa_circ_288279,RMVar_hsa_circ_221692,RMVar_hsa_circ_221689,RMVar_hsa_circ_221690,RMVar_hsa_circ_221688 105750 RMVar_ID_105750 Human_SNP_ID_155259879 m1A Human chr3 - 138608676 138608676 138608676 ACGGACCCAACCCTGGTCCTCTGCCTTAGCCGAAGGCCGCACCCTCCGCGCATAGGCCTTCCTCA ACGGACCCAACCCTGGTCCTCTGCCTTAGCCGGAGGCCGCACCCTCCGCGCATAGGCCTTCCTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:138608635..138608743 26863196 MeRIP-seq:(Medium) rs1019160506 Functional Loss SNV dbSNP153 33..33 33 - - - 105751 RMVar_ID_105751 Human_SNP_ID_155259944 m1A Human chr3 + 138608884 138608884 138608884 GCCACGCGGCCTACGCAGCCGAGTCGGAACCAACCGGTTGTTTGGTGAAACCTACCCCAGAGCCT GCCACGCGGCCTACGCAGCCGAGTCGGAACCACCCGGTTGTTTGGTGAAACCTACCCCAGAGCCT A C FAIM Ensembl:ENSG00000158234 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138608833..138609160 26863196 MeRIP-seq:(Medium) rs1022954846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4758413 Human_Splice_Rec_489267,Human_Splice_Rec_489275,Human_Splice_Rec_489285,Human_Splice_Rec_489295 105752 RMVar_ID_105752 Human_SNP_ID_155259950 m1A Human chr3 - 138608916 138608916 138608916 TGCTGCCTCACCTGTGCTCTGTGGGCCGCGGGAGGCTCTGGGGTAGGTTTCACCAAACAACCGGT TGCTGCCTCACCTGTGCTCTGTGGGCCGCGGGGGGCTCTGGGGTAGGTTTCACCAAACAACCGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138608623..138609016 26863196 MeRIP-seq:(Medium) rs1055855464 Functional Loss SNV dbSNP153 33..33 33 - - - 105753 RMVar_ID_105753 Human_SNP_ID_155260014 m1A Human chr3 - 138609082 138609082 138609082 GCGCAAACACCGCCCGCCGCCGCCGCCCAGAGATGGCCGCCGCCGGCGCAGCAGGGCCGAGAGCG GCGCAAACACCGCCCGCCGCCGCCGCCCAGAGTTGGCCGCCGCCGGCGCAGCAGGGCCGAGAGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:138609076..138609190 26863196 MeRIP-seq:(Medium) rs1389213023 Functional Loss SNV dbSNP153 33..33 33 - - - 105754 RMVar_ID_105754 Human_SNP_ID_155315574 m1A Human chr3 + 138834802 138834802 138834802 CCACTCCGGCGCCCCCATCCCTGCCTCTCTCGATCACCTCCCGCCTGCCCCGCGCAGCACTACAC CCACTCCGGCGCCCCCATCCCTGCCTCTCTCGCTCACCTCCCGCCTGCCCCGCGCAGCACTACAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:138834676..138834925;chr3:138834647..138834925 26863196 MeRIP-seq:(Medium) rs1054547092 Functional Loss SNV dbSNP153 33..33 33 - - - 105755 RMVar_ID_105755 Human_SNP_ID_155344796 m1A Human chr3 + 138945378 138945378 138945378 GCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGAGGTGAGCACAGGAGGACATAAACTGAGGGGAC GCCAGGGGAGTGCAAGGTCACAGAGGTCAGGGGGGTGAGCACAGGAGGACATAAACTGAGGGGAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:138945281..138945532 26863196 MeRIP-seq:(Medium) rs1048558809 Functional Loss SNV dbSNP153 33..33 33 - - - 105756 RMVar_ID_105756 Human_SNP_ID_155344835 m1A Human chr3 - 138945516 138945516 138945516 ACGCGCGACGCCGGCCCCGGTCGCAGCCGACGACGCCGCCGCCAGCCTGACCTCACACCCTCTGG ACGCGCGACGCCGGCCCCGGTCGCAGCCGACGCCGCCGCCGCCAGCCTGACCTCACACCCTCTGG T G FOXL2 Ensembl:ENSG00000183770 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:138945292..138945576 26863196 MeRIP-seq:(Medium) rs1466257052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27498561 105757 RMVar_ID_105757 Human_SNP_ID_155344968 m1A Human chr3 - 138945761 138945761 138945761 GCACCACGGGGCCGCCGCGCCGCCGCCGGGCCAGCTCAGCCCTGCCAGCCCAGCCACCGCCGCGC GCACCACGGGGCCGCCGCGCCGCCGCCGGGCCGGCTCAGCCCTGCCAGCCCAGCCACCGCCGCGC T C FOXL2 Ensembl:ENSG00000183770 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:138945664..138945944 26863196 MeRIP-seq:(Medium) rs1282430998 Functional Loss SNV dbSNP153 33..33 33 - - - 105758 RMVar_ID_105758 Human_SNP_ID_155345553 m1A Human chr3 - 138947027 138947027 138947027 CCGGGGGGCGGGGGGAGGGGAAGAGCGCAGAAAAGAAAACCCACCAAGGCGGGGACTGGCCTGAG CCGGGGGGCGGGGGGAGGGGAAGAGCGCAGAAGAGAAAACCCACCAAGGCGGGGACTGGCCTGAG T C FOXL2 Ensembl:ENSG00000183770 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:138946595..138947125 26863196 MeRIP-seq:(Medium) rs941874514 Functional Loss SNV dbSNP153 33..33 33 - - - 105759 RMVar_ID_105759 Human_SNP_ID_155439803 m1A Human chr3 - 139344077 139344077 139344077 CGAGCCCGGAAACAGACCCGTTCCACGCCCGGAGAACTCCTCAAGAGGCTCCACAGCAATACAGT CGAGCCCGGAAACAGACCCGTTCCACGCCCGGGGAACTCCTCAAGAGGCTCCACAGCAATACAGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:139344026..139344163 26863196 MeRIP-seq:(Medium) rs1411404317 Functional Loss SNV dbSNP153 33..33 33 - - - 105760 RMVar_ID_105760 Human_SNP_ID_155444327 m1A Human chr3 - 139361169 139361169 139361169 GGGGCCTGCTGCTTTTGGCCACTGCCTCTGGAAATGCTAATATGGTGAACAAGCTAGCAGAGGGT GGGGCCTGCTGCTTTTGGCCACTGCCTCTGGACATGCTAATATGGTGAACAAGCTAGCAGAGGGT T G COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:139359159..139366628 32194978 MeRIP-seq:(Medium) rs748398802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11571,Human_RBP_ID_8868108,Human_RBP_ID_9132813,Human_RBP_ID_9394131,Human_RBP_ID_18194947,Human_RBP_ID_18798190,Human_RBP_ID_22455593,Human_RBP_ID_26347244 Human_Splice_Rec_489843,Human_Splice_Rec_489885 Human_miRNA_ID_1605300,Human_miRNA_ID_1679547,Human_miRNA_ID_2824150,Human_miRNA_ID_2858122 RMVar_hsa_circ_21046,RMVar_hsa_circ_111438,RMVar_hsa_circ_121631,RMVar_hsa_circ_128169,RMVar_hsa_circ_119393,RMVar_hsa_circ_103134,RMVar_hsa_circ_106324,RMVar_hsa_circ_96987,RMVar_hsa_circ_221749,RMVar_hsa_circ_79307,RMVar_hsa_circ_93453,RMVar_hsa_circ_93549,RMVar_hsa_circ_88898,RMVar_hsa_circ_221753,RMVar_hsa_circ_221755,RMVar_hsa_circ_221756,RMVar_hsa_circ_221754,RMVar_hsa_circ_221751,RMVar_hsa_circ_221752,RMVar_hsa_circ_221750,RMVar_hsa_circ_103906,RMVar_hsa_circ_221747,RMVar_hsa_circ_221748,RMVar_hsa_circ_221746,RMVar_hsa_circ_221758,RMVar_hsa_circ_64109,RMVar_hsa_circ_335729,RMVar_hsa_circ_348730,RMVar_hsa_circ_101913,RMVar_hsa_circ_84955,RMVar_hsa_circ_221759,RMVar_hsa_circ_292507,RMVar_hsa_circ_221760,RMVar_hsa_circ_65898 105761 RMVar_ID_105761 Human_SNP_ID_155446738 m1A Human chr3 - 139371802 139371802 139371802 GGTTTGTGGTGGTGTGTGGTGATGGGGAGTATATCATCTACACAGCAATGGCATTGAGAAACAAG GGTTTGTGGTGGTGTGTGGTGATGGGGAGTATGTCATCTACACAGCAATGGCATTGAGAAACAAG T C COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:139371751..139374264 32194978 MeRIP-seq:(Medium) rs1263754828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8875646,Human_RBP_ID_9132819,Human_RBP_ID_9354424,Human_RBP_ID_22457018,Human_RBP_ID_25763208 Human_Splice_Rec_489828,Human_Splice_Rec_489829,Human_Splice_Rec_489870,Human_Splice_Rec_489871,Human_Splice_Rec_489897 RMVar_hsa_circ_121631,RMVar_hsa_circ_119393,RMVar_hsa_circ_103134,RMVar_hsa_circ_106324,RMVar_hsa_circ_96987,RMVar_hsa_circ_221749,RMVar_hsa_circ_93453,RMVar_hsa_circ_221751,RMVar_hsa_circ_221750,RMVar_hsa_circ_103906,RMVar_hsa_circ_221747,RMVar_hsa_circ_221748,RMVar_hsa_circ_221746,RMVar_hsa_circ_221758,RMVar_hsa_circ_348730,RMVar_hsa_circ_101913,RMVar_hsa_circ_57059,RMVar_hsa_circ_221759,RMVar_hsa_circ_65898,RMVar_hsa_circ_37084 105762 RMVar_ID_105762 Human_SNP_ID_155448479 m1A Human chr3 - 139379452 139379452 139379452 TCTTGTTACATTTTAAAGACACTGGTGAAGACATTTGAAGTATGTGATCTTCCTGTTCGAGCTGC TCTTGTTACATTTTAAAGACACTGGTGAAGACGTTTGAAGTATGTGATCTTCCTGTTCGAGCTGC T C COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:139379123..139379784 32194978 MeRIP-seq:(Medium) rs770419250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9348946,Human_RBP_ID_22676718,Human_RBP_ID_22768720,Human_RBP_ID_23973122,Human_RBP_ID_27823514 Human_Splice_Rec_489814,Human_Splice_Rec_489815,Human_Splice_Rec_489856,Human_Splice_Rec_489857,Human_Splice_Rec_489908,Human_Splice_Rec_489909,Human_Splice_Rec_489920,Human_Splice_Rec_489921,Human_Splice_Rec_489930,Human_Splice_Rec_489931,Human_Splice_Rec_489940,Human_Splice_Rec_489941,Human_Splice_Rec_489948,Human_Splice_Rec_489949,Human_Splice_Rec_489958,Human_Splice_Rec_489959,Human_Splice_Rec_489966,Human_Splice_Rec_489967 RMVar_hsa_circ_106324,RMVar_hsa_circ_93453,RMVar_hsa_circ_103906,RMVar_hsa_circ_221747,RMVar_hsa_circ_221746,RMVar_hsa_circ_221758,RMVar_hsa_circ_348730,RMVar_hsa_circ_28305,RMVar_hsa_circ_65898,RMVar_hsa_circ_4452,RMVar_hsa_circ_59923 105763 RMVar_ID_105763 Human_SNP_ID_155449977 m1A Human chr3 - 139386139 139386139 139386139 TTTAAAGTAAGAGGTAAAGGTTGTTGCTGAAAATGAAGGAGGCGTGGGTAGAACAAGACTTGAAG TTTAAAGTAAGAGGTAAAGGTTGTTGCTGAAAGTGAAGGAGGCGTGGGTAGAACAAGACTTGAAG T C COPB2 Ensembl:ENSG00000184432 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:139386135..139386239 26863196 MeRIP-seq:(Medium) rs9871030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14647021 GWAS_ID_14539,GWAS_ID_14540,GWAS_ID_14541 105764 RMVar_ID_105764 Human_SNP_ID_155450907 m1A Human chr3 - 139389582 139389582 139389582 GTTTATCTCAAGGCCTGAGTAGCCGGTAACAAACGAGGGTTCCCGGGATTGGACCGACGCAGCCA GTTTATCTCAAGGCCTGAGTAGCCGGTAACAAGCGAGGGTTCCCGGGATTGGACCGACGCAGCCA T C COPB2 Ensembl:ENSG00000184432 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:139389371..139389581 26863196 MeRIP-seq:(Medium) rs759119932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1310156,Human_RBP_ID_1618823,Human_RBP_ID_4757478,Human_RBP_ID_5325327,Human_RBP_ID_8875652,Human_RBP_ID_8943579,Human_RBP_ID_18424492,Human_RBP_ID_22457022,Human_RBP_ID_23213611,Human_RBP_ID_23973139 Human_Splice_Rec_489811,Human_Splice_Rec_489905,Human_Splice_Rec_489917,Human_Splice_Rec_489943,Human_Splice_Rec_489951,Human_Splice_Rec_489961,Human_Splice_Rec_489969 105765 RMVar_ID_105765 Human_SNP_ID_155450919 m1A Human chr3 + 139389599 139389599 139389599 TCCCGGGAACCCTCGTTTGTTACCGGCTACTCAGGCCTTGAGATAAACCCACCGATCCACTGACC TCCCGGGAACCCTCGTTTGTTACCGGCTACTCGGGCCTTGAGATAAACCCACCGATCCACTGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:139389487..139389650;chr3:139389393..139389611;chr3:139389489..139389605 26863196 MeRIP-seq:(Medium) rs1402922956 Functional Loss SNV dbSNP153 33..33 33 - - - 105766 RMVar_ID_105766 Human_SNP_ID_155451051 m1A Human chr3 - 139389903 139389903 139389903 GCCCTGCAGTTAGCGTCCAGCGGGGATTAGGCACTTCGTTTTCCTCATCGTTTCAATCTCTATCT GCCCTGCAGTTAGCGTCCAGCGGGGATTAGGCTCTTCGTTTTCCTCATCGTTTCAATCTCTATCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:139389853..139389991 26863196 MeRIP-seq:(Medium) rs908877235 Functional Loss SNV dbSNP153 33..33 33 - - - 105767 RMVar_ID_105767 Human_SNP_ID_155823477 m1A Human chr3 - 140942025 140942025 140942025 CATTCTCTCTCCCGCATGTCCTCCGGCCGCTGAGGCGGGACGCGGATCTGGCCGCCCGCTACGGC CATTCTCTCTCCCGCATGTCCTCCGGCCGCTGGGGCGGGACGCGGATCTGGCCGCCCGCTACGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:140941974..140942050 26863196 MeRIP-seq:(Medium) rs759623094 Functional Loss SNV dbSNP153 33..33 33 - - - 105768 RMVar_ID_105768 Human_SNP_ID_155830481 m1A Human chr3 - 140969680 140969680 140969680 AGGTGTATCTACATATGCAAAATAATTACACTAAATTGTTTCCAAAGCTGAATTTGGTCTCACAG AGGTGTATCTACATATGCAAAATAATTACACTGAATTGTTTCCAAAGCTGAATTTGGTCTCACAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:140969671..140969762 32194978 MeRIP-seq:(Medium) rs1278262901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221791 105769 RMVar_ID_105769 Human_SNP_ID_155901325 m1A Human chr3 + 141260172 141260170 141260173 AGGTGAAACCATGAAGAGAAAATAGAATACTTAATAATGCTTTTCCGCAACCGCTTCTTGCTGCT AGGTGAAACCATGAAGAGAAAATAGAATACT___TAATGCTTTTCCGCAACCGCTTCTTGCTGCT TTAA T PXYLP1 Ensembl:ENSG00000155893 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:141260094..141260214 26863196 MeRIP-seq:(Medium) rs1231863736 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_490542,Human_Splice_Rec_490543,Human_Splice_Rec_490550,Human_Splice_Rec_490551,Human_Splice_Rec_490566,Human_Splice_Rec_490567,Human_Splice_Rec_490572,Human_Splice_Rec_490573,Human_Splice_Rec_490582,Human_Splice_Rec_490583,Human_Splice_Rec_490598,Human_Splice_Rec_490599,Human_Splice_Rec_490614,Human_Splice_Rec_490615,Human_Splice_Rec_490630,Human_Splice_Rec_490631,Human_Splice_Rec_490642,Human_Splice_Rec_490643,Human_Splice_Rec_490658,Human_Splice_Rec_490659,Human_Splice_Rec_490661 Human_miRNA_ID_1976837 RMVar_hsa_circ_313984,RMVar_hsa_circ_367532,RMVar_hsa_circ_221799,RMVar_hsa_circ_306245,RMVar_hsa_circ_221798 105770 RMVar_ID_105770 Human_SNP_ID_155931535 m1A Human chr3 - 141393741 141393741 141393741 TTCCCACTTTCTCCCTGGTACCTTGTTCCCCCAGCTCCATGGCGCAGCAGAGCGGCATCTCCTTT TTCCCACTTTCTCCCTGGTACCTTGTTCCCCCCGCTCCATGGCGCAGCAGAGCGGCATCTCCTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:141393570..141393777 26863196 MeRIP-seq:(Medium) rs1259333255 Functional Loss SNV dbSNP153 33..33 33 - - - 105771 RMVar_ID_105771 Human_SNP_ID_155938715 m1A Human chr3 + 141427437 141427437 141427437 TGCCCAGGCTAGAAGGACATTCCAGGCTGCAGAAGCAGCATGTGCAAACGCCCTGGGCTGGGAAG TGCCCAGGCTAGAAGGACATTCCAGGCTGCAGTAGCAGCATGTGCAAACGCCCTGGGCTGGGAAG A T ZBTB38 Ensembl:ENSG00000177311 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:141427406..141427522 26863196 MeRIP-seq:(Medium) rs761539014 Functional Loss SNV dbSNP153 33..33 33 - - - 105772 RMVar_ID_105772 Human_SNP_ID_155943026 m1A Human chr3 - 141445352 141445352 141445352 CCTTGGTTTCCAGCCCCCACTGCTTTGTCTCCATCACAGAGTTCACACTGCAGCTTGGGCATCTC CCTTGGTTTCCAGCCCCCACTGCTTTGTCTCCGTCACAGAGTTCACACTGCAGCTTGGGCATCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:141445301..141445450 32194978 MeRIP-seq:(Medium) rs1484468697 Functional Loss SNV dbSNP153 33..33 33 - - - 105773 RMVar_ID_105773 Human_SNP_ID_155953218 m1A Human chr3 + 141487465 141487465 141487465 AGTGGGAGCTGGAGATGGGCCTGGGGTGGGAGAGCCCGGGCTGCGCCGGCGTGAGGGGCTCGGTC AGTGGGAGCTGGAGATGGGCCTGGGGTGGGAGGGCCCGGGCTGCGCCGGCGTGAGGGGCTCGGTC A G RASA2 Ensembl:ENSG00000155903 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:141487449..141487645 26863196 MeRIP-seq:(Medium) rs1460609440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266602,Human_RBP_ID_3720923,Human_RBP_ID_5392217,Human_RBP_ID_8209484,Human_RBP_ID_9333895,Human_RBP_ID_9354426,Human_RBP_ID_9434943,Human_RBP_ID_22608811,Human_RBP_ID_26790854 105774 RMVar_ID_105774 Human_SNP_ID_156013904 m1A Human chr3 - 141738323 141738323 141738323 TCCACGTCGGCCATGGCGGCGCCGCGGAGCCGACGGCGGAGACGTTGGCTTGGGGAAGGCGGAAG TCCACGTCGGCCATGGCGGCGCCGCGGAGCCGGCGGCGGAGACGTTGGCTTGGGGAAGGCGGAAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:141738226..141738378 26863410 MeRIP-seq:(Medium) rs1419455866 Functional Loss SNV dbSNP153 33..33 33 - - - 105775 RMVar_ID_105775 Human_SNP_ID_156024933 m1A Human chr3 + 141783512 141783512 141783512 CACAGGAGCCAAAGAAGAGGATTTCAGGGAGGAAAGTGTGGTCAAAGTGTCAAGTGTTGCAAAGA CACAGGAGCCAAAGAAGAGGATTTCAGGGAGGGAAGTGTGGTCAAAGTGTCAAGTGTTGCAAAGA A G AC112504.2,GRK7 Ensembl:ENSG00000285558,Ensembl:ENSG00000114124 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:141783468..141783537 26863196 MeRIP-seq:(Medium) rs992140182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14650049 105776 RMVar_ID_105776 Human_SNP_ID_156047927 m1A Human chr3 + 141876319 141876310 141876320 GGTAGCATCTTCTCAGCGCCCCGGCGCCCAGGAACGCCCAGGAAACCCAGTCCTCCTCCTAAGCA GGTAGCATCTTCTCAGCGCCCCGG__________CGCCCAGGAAACCCAGTCCTCCTCCTAAGCA GCGCCCAGGAA G ATP1B3 Ensembl:ENSG00000069849 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:141876201..141876425 26863196 MeRIP-seq:(Medium) rs879385601 Functional Loss DEL dbSNP153 25..34 33 - - - Human_Splice_Rec_491045 105777 RMVar_ID_105777 Human_SNP_ID_156056612 m1A Human chr3 + 141909514 141909514 141909514 CAGAGTGGTCTGGGAAAGCCTTATGGAAAGGGAACCTTGAGGGAAGAGCTGAAGGAGGTGAAAGA CAGAGTGGTCTGGGAAAGCCTTATGGAAAGGGGACCTTGAGGGAAGAGCTGAAGGAGGTGAAAGA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:141909510..141909655 26863196 MeRIP-seq:(Medium) rs778892837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14650925 RMVar_hsa_circ_22382,RMVar_hsa_circ_310076,RMVar_hsa_circ_49898,RMVar_hsa_circ_221856,RMVar_hsa_circ_221858,RMVar_hsa_circ_278414,RMVar_hsa_circ_309092,RMVar_hsa_circ_346125,RMVar_hsa_circ_904 105778 RMVar_ID_105778 Human_SNP_ID_156082149 m1A Human chr3 - 142005486 142005486 142005486 GTTTCCAATACCAACTCACCTACAAAGATTTTACCAAAAACCTTAGGACCAATAAATGTGAATGT GTTTCCAATACCAACTCACCTACAAAGATTTTGCCAAAAACCTTAGGACCAATAAATGTGAATGT T C TFDP2 Ensembl:ENSG00000114126 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7627056 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_17291574,Human_RBP_ID_17401858 Human_Splice_Rec_491134,Human_Splice_Rec_491135,Human_Splice_Rec_491172,Human_Splice_Rec_491173,Human_Splice_Rec_491206,Human_Splice_Rec_491207,Human_Splice_Rec_491230,Human_Splice_Rec_491231,Human_Splice_Rec_491249,Human_Splice_Rec_491270,Human_Splice_Rec_491271,Human_Splice_Rec_491296,Human_Splice_Rec_491297,Human_Splice_Rec_491324,Human_Splice_Rec_491325,Human_Splice_Rec_491348,Human_Splice_Rec_491349,Human_Splice_Rec_491352,Human_Splice_Rec_491353,Human_Splice_Rec_491362,Human_Splice_Rec_491363,Human_Splice_Rec_491368,Human_Splice_Rec_491369,Human_Splice_Rec_491374,Human_Splice_Rec_491375,Human_Splice_Rec_491382,Human_Splice_Rec_491383,Human_Splice_Rec_491396,Human_Splice_Rec_491397 GWAS_ID_14542,GWAS_ID_14543,GWAS_ID_14544,GWAS_ID_14545,GWAS_ID_14546,GWAS_ID_14547,GWAS_ID_14548,GWAS_ID_14549,GWAS_ID_14550,GWAS_ID_14551,GWAS_ID_14552,GWAS_ID_14553 RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_294302,RMVar_hsa_circ_17243,RMVar_hsa_circ_73369,RMVar_hsa_circ_221860,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_316443,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_40191,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_290615,RMVar_hsa_circ_348867,RMVar_hsa_circ_221869,RMVar_hsa_circ_324638,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872 105779 RMVar_ID_105779 Human_SNP_ID_156084415 m1A Human chr3 + 142014975 142014975 142014975 TCTTTTGAACCCTCTCTTCCCAATTTTCCCCCACAATTCCACTGAAATTCTTGGCCTTCAATTTA TCTTTTGAACCCTCTCTTCCCAATTTTCCCCCGCAATTCCACTGAAATTCTTGGCCTTCAATTTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:142014954..142015174 26863196 MeRIP-seq:(Medium) rs1197434449 Functional Loss SNV dbSNP153 33..33 33 - - - 105780 RMVar_ID_105780 Human_SNP_ID_156115737 m1A Human chr3 + 142149441 142149441 142149441 AGGGCGCGCCCCGCGGGCCGGGCAGCTGCGGCAGCGCCGCAGCCGAGATCGCTACCGATTTCGTC AGGGCGCGCCCCGCGGGCCGGGCAGCTGCGGCCGCGCCGCAGCCGAGATCGCTACCGATTTCGTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:142149390..142149481 26863196 MeRIP-seq:(Medium) rs190051545 Functional Loss SNV dbSNP153 33..33 33 - - - 105781 RMVar_ID_105781 Human_SNP_ID_156115747 m1A Human chr3 - 142149457 142149457 142149457 GGGCAGGGAGAGGGCGGACGAAATCGGTAGCGATCTCGGCTGCGGCGCTGCCGCAGCTGCCCGGC GGGCAGGGAGAGGGCGGACGAAATCGGTAGCGGTCTCGGCTGCGGCGCTGCCGCAGCTGCCCGGC T C TFDP2 Ensembl:ENSG00000114126 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:142149409..142149474 26863196 MeRIP-seq:(Medium) rs548244512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785221,Human_RBP_ID_4756768,Human_RBP_ID_18424061,Human_RBP_ID_22457028 105782 RMVar_ID_105782 Human_SNP_ID_156115748 m1A Human chr3 - 142149457 142149457 142149457 GGGCAGGGAGAGGGCGGACGAAATCGGTAGCGATCTCGGCTGCGGCGCTGCCGCAGCTGCCCGGC GGGCAGGGAGAGGGCGGACGAAATCGGTAGCGCTCTCGGCTGCGGCGCTGCCGCAGCTGCCCGGC T G TFDP2 Ensembl:ENSG00000114126 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:142149409..142149474 26863196 MeRIP-seq:(Medium) rs548244512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785221,Human_RBP_ID_4756768,Human_RBP_ID_18424061,Human_RBP_ID_22457028 105783 RMVar_ID_105783 Human_SNP_ID_156120283 m1A Human chr3 - 142168900 142168900 142168900 GTAAGAGATGGTTGGCTCAATATCCCTATTGCAACTTGTGCAAAGGCATTCATCAATGATGGGAA GTAAGAGATGGTTGGCTCAATATCCCTATTGCTACTTGTGCAAAGGCATTCATCAATGATGGGAA T A GK5 Ensembl:ENSG00000175066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:142168850..142169062 26863196 MeRIP-seq:(Medium) rs79504759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_335227,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221876,RMVar_hsa_circ_221877 105784 RMVar_ID_105784 Human_SNP_ID_156133313 m1A Human chr3 + 142225482 142225482 142225482 CGACATCCCGATCCCGCACGCCTCTCCGCTACAGCCGCCTACCCAGAGGGCGCGCTACAAATCCC CGACATCCCGATCCCGCACGCCTCTCCGCTACGGCCGCCTACCCAGAGGGCGCGCTACAAATCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:142225436..142225568 26863196 MeRIP-seq:(Medium) rs1183293620 Functional Loss SNV dbSNP153 33..33 33 - - - 105785 RMVar_ID_105785 Human_SNP_ID_156209201 m1A Human chr3 - 142543649 142543649 142543649 AAAGAAGAGGAGAGAAAAGAAAAAAGAGAGAGAAAGGAGGAAAGAAAGAAATAGAAAGGAAGGAA AAAGAAGAGGAGAGAAAAGAAAAAAGAGAGAGGAAGGAGGAAAGAAAGAAATAGAAAGGAAGGAA T C ATR Ensembl:ENSG00000175054 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:142543523..142543721 26863196 MeRIP-seq:(Medium) rs1289440053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116041,RMVar_hsa_circ_7513,RMVar_hsa_circ_221944,RMVar_hsa_circ_120654,RMVar_hsa_circ_221946,RMVar_hsa_circ_114937,RMVar_hsa_circ_221952,RMVar_hsa_circ_280654,RMVar_hsa_circ_56898,RMVar_hsa_circ_221953,RMVar_hsa_circ_78247,RMVar_hsa_circ_221955,RMVar_hsa_circ_352628,RMVar_hsa_circ_333774,RMVar_hsa_circ_68552,RMVar_hsa_circ_32185,RMVar_hsa_circ_221963,RMVar_hsa_circ_15916,RMVar_hsa_circ_281517,RMVar_hsa_circ_266358,RMVar_hsa_circ_46152,RMVar_hsa_circ_62722,RMVar_hsa_circ_337363,RMVar_hsa_circ_74913,RMVar_hsa_circ_55661,RMVar_hsa_circ_351226,RMVar_hsa_circ_371853,RMVar_hsa_circ_277955,RMVar_hsa_circ_95186,RMVar_hsa_circ_221969,RMVar_hsa_circ_221971,RMVar_hsa_circ_221972,RMVar_hsa_circ_221970,RMVar_hsa_circ_332311,RMVar_hsa_circ_60665,RMVar_hsa_circ_340744,RMVar_hsa_circ_57313,RMVar_hsa_circ_372679,RMVar_hsa_circ_221974,RMVar_hsa_circ_39547,RMVar_hsa_circ_116967,RMVar_hsa_circ_23120,RMVar_hsa_circ_221976,RMVar_hsa_circ_71021,RMVar_hsa_circ_299505,RMVar_hsa_circ_369884,RMVar_hsa_circ_221979,RMVar_hsa_circ_221980,RMVar_hsa_circ_221978,RMVar_hsa_circ_265385,RMVar_hsa_circ_13791,RMVar_hsa_circ_302500,RMVar_hsa_circ_346920,RMVar_hsa_circ_356996,RMVar_hsa_circ_72400,RMVar_hsa_circ_319698,RMVar_hsa_circ_377901,RMVar_hsa_circ_221981,RMVar_hsa_circ_332477,RMVar_hsa_circ_307293,RMVar_hsa_circ_30458,RMVar_hsa_circ_68546,RMVar_hsa_circ_27955,RMVar_hsa_circ_4474,RMVar_hsa_circ_52863,RMVar_hsa_circ_96969,RMVar_hsa_circ_221982,RMVar_hsa_circ_221983,RMVar_hsa_circ_71422,RMVar_hsa_circ_72998,RMVar_hsa_circ_42494,RMVar_hsa_circ_43652,RMVar_hsa_circ_14854,RMVar_hsa_circ_221984 105786 RMVar_ID_105786 Human_SNP_ID_156222291 m1A Human chr3 + 142596473 142596473 142596473 GTGGACCTGCAGGTACTTGGATCTCCAGTGGGAGCTGCCCTCTCGAAGGCAGGACAGCGGTGGCG GTGGACCTGCAGGTACTTGGATCTCCAGTGGGTGCTGCCCTCTCGAAGGCAGGACAGCGGTGGCG A T PLS1 Ensembl:ENSG00000120756 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:142596424..142596520 26863196 MeRIP-seq:(Medium) rs1048311953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757495 Human_Splice_Rec_492499,Human_Splice_Rec_492529,Human_Splice_Rec_492537,Human_Splice_Rec_492545,Human_Splice_Rec_492551,Human_Splice_Rec_492567,Human_Splice_Rec_492573 105787 RMVar_ID_105787 Human_SNP_ID_156238657 m1A Human chr3 + 142669323 142669322 142669323 AAGGCTCTGTCTGCACATCTATGAATCCTCCCAAAAGGCATCCTTATTGTACACCTTCAACAAAG AAGGCTCTGTCTGCACATCTATGAATCCTCCC_AAAGGCATCCTTATTGTACACCTTCAACAAAG CA C PLS1 Ensembl:ENSG00000120756 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:142669322..142669407 26863196 MeRIP-seq:(Medium) rs1433796757 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_73559,RMVar_hsa_circ_285636 105788 RMVar_ID_105788 Human_SNP_ID_156287710 m1A Human chr3 - 142888904 142888904 142888904 CGCGCGCCGTGGGGTGCAAACCCCGAGCGTCTACGCTGCCATGAGGGGCGCGAACGCCTGGGCGC CGCGCGCCGTGGGGTGCAAACCCCGAGCGTCTGCGCTGCCATGAGGGGCGCGAACGCCTGGGCGC T C PCOLCE2 Ensembl:ENSG00000163710 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:142888853..142889182 26863196 MeRIP-seq:(Medium) rs1386283741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4725858 Human_Splice_Rec_492741,Human_Splice_Rec_492763,Human_Splice_Rec_492779,Human_Splice_Rec_492809,Human_Splice_Rec_492815,Human_Splice_Rec_492823 105789 RMVar_ID_105789 Human_SNP_ID_156314566 m1A Human chr3 + 143001143 143001138 143001144 AACATTCACCATCTTAAGATGAGCAGACTGCAAGTTTGCCTCTCCCACCAGTATGGGAGCTGCCG AACATTCACCATCTTAAGATGAGCAGAC______TTTGCCTCTCCCACCAGTATGGGAGCTGCCG CTGCAAG C U2SURP,PAQR9-AS1 Ensembl:ENSG00000163714,Ensembl:ENSG00000241570 Protein coding,lincRNA intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:143001095..143001173 32194978 MeRIP-seq:(Medium) rs1180258536 Functional Loss DEL dbSNP153 29..34 33 - - - 105790 RMVar_ID_105790 Human_SNP_ID_156314769 m1A Human chr3 + 143001671 143001671 143001671 AAACGCCAGGCGGATCTCAGAAGGCCAGTTCAAAGGTAATTTCTGACAAAATTTCGTAAGTCAGC AAACGCCAGGCGGATCTCAGAAGGCCAGTTCAGAGGTAATTTCTGACAAAATTTCGTAAGTCAGC A G U2SURP Ensembl:ENSG00000163714 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr3:143001638..143001717;chr3:143001646..143001720;chr3:143001646..143001740;chr3:143001651..143001675 26863196,32194978 MeRIP-seq:(Medium) rs1560169276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757496,Human_RBP_ID_9394144,Human_RBP_ID_18424065,Human_RBP_ID_19116199,Human_RBP_ID_27822547 Human_Splice_Rec_493023,Human_Splice_Rec_493073,Human_Splice_Rec_493083,Human_Splice_Rec_493135,Human_Splice_Rec_493157,Human_Splice_Rec_493211,Human_Splice_Rec_493265 105791 RMVar_ID_105791 Human_SNP_ID_156317793 m1A Human chr3 + 143012301 143012301 143012301 ACCTAAGAGCCCAAGAAAACATAATTATAGGAATGAAAGTGCCCGTGAAAGCCTTTGTGATTCTC ACCTAAGAGCCCAAGAAAACATAATTATAGGAGTGAAAGTGCCCGTGAAAGCCTTTGTGATTCTC A G U2SURP Ensembl:ENSG00000163714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:143012251..143012325 26863196 MeRIP-seq:(Medium) rs1465944994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1951443,Human_RBP_ID_2753673,Human_RBP_ID_8561070,Human_RBP_ID_14657716,Human_RBP_ID_23974966,Human_RBP_ID_26347257 Human_Splice_Rec_493018,Human_Splice_Rec_493019,Human_Splice_Rec_493026,Human_Splice_Rec_493027,Human_Splice_Rec_493076,Human_Splice_Rec_493077,Human_Splice_Rec_493086,Human_Splice_Rec_493087,Human_Splice_Rec_493138,Human_Splice_Rec_493139,Human_Splice_Rec_493160,Human_Splice_Rec_493161,Human_Splice_Rec_493214,Human_Splice_Rec_493215,Human_Splice_Rec_493268,Human_Splice_Rec_493269,Human_Splice_Rec_493286,Human_Splice_Rec_493287,Human_Splice_Rec_493294,Human_Splice_Rec_493295,Human_Splice_Rec_493301 Human_miRNA_ID_2439425 RMVar_hsa_circ_32599,RMVar_hsa_circ_354873,RMVar_hsa_circ_366568,RMVar_hsa_circ_377475,RMVar_hsa_circ_73220,RMVar_hsa_circ_366991,RMVar_hsa_circ_356024,RMVar_hsa_circ_71890,RMVar_hsa_circ_327972,RMVar_hsa_circ_56230,RMVar_hsa_circ_222033 105792 RMVar_ID_105792 Human_SNP_ID_156328902 m1A Human chr3 + 143053775 143053775 143053775 GCTCCAAAGACAAGAAGGAAAAAGATGAGTGTACTCCGACAAGGAAGGAAAGGTATAACATTTCT GCTCCAAAGACAAGAAGGAAAAAGATGAGTGTGCTCCGACAAGGAAGGAAAGGTATAACATTTCT A G U2SURP Ensembl:ENSG00000163714 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:143053676..143053800 26863196 MeRIP-seq:(Medium) rs1347593303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68415,Human_RBP_ID_247565,Human_RBP_ID_783687,Human_RBP_ID_937019,Human_RBP_ID_23975169,Human_RBP_ID_24547311,Human_RBP_ID_26347276,Human_RBP_ID_27046947 Human_Splice_Rec_493068,Human_Splice_Rec_493069,Human_Splice_Rec_493130,Human_Splice_Rec_493131,Human_Splice_Rec_493206,Human_Splice_Rec_493207,Human_Splice_Rec_493260,Human_Splice_Rec_493261,Human_Splice_Rec_493342,Human_Splice_Rec_493364,Human_Splice_Rec_493365 RMVar_hsa_circ_81353,RMVar_hsa_circ_116960,RMVar_hsa_circ_108737,RMVar_hsa_circ_222036,RMVar_hsa_circ_222039,RMVar_hsa_circ_24022,RMVar_hsa_circ_14575,RMVar_hsa_circ_222040 105793 RMVar_ID_105793 Human_SNP_ID_157057047 m1A Human chr3 + 146015466 146015466 146015466 TCACCTCTTCCTTTCTCTCCCCGCCTCCTTATATTTCTTTTCCCTCTCCTCCTCCCTCTCCTCAT TCACCTCTTCCTTTCTCTCCCCGCCTCCTTATGTTTCTTTTCCCTCTCCTCCTCCCTCTCCTCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:146015346..146015723 26863196 MeRIP-seq:(Medium) rs1446290042 Functional Loss SNV dbSNP153 33..33 33 - - - 105794 RMVar_ID_105794 Human_SNP_ID_157062710 m1A Human chr3 - 146038647 146038647 146038647 GGAACAAATGGAGTGAAATGAGGAAGTAGTCCATGGGAAGCCGAAGCTGAAGGCTCAGTAGAAAC GGAACAAATGGAGTGAAATGAGGAAGTAGTCCGTGGGAAGCCGAAGCTGAAGGCTCAGTAGAAAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:146038601..146038685 26863196 MeRIP-seq:(Medium) rs1483707043 Functional Loss SNV dbSNP153 33..33 33 - - - 105795 RMVar_ID_105795 Human_SNP_ID_157070296 m1A Human chr3 - 146070874 146070874 146070874 AATCTGATGTATTTCTTCATTTTAACTTTTTTAGGGAGGTGGTTGCAAATTTCTAAGGTACAATT AATCTGATGTATTTCTTCATTTTAACTTTTTTGGGGAGGTGGTTGCAAATTTCTAAGGTACAATT T C PLOD2 Ensembl:ENSG00000152952 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:146070838..146071158 32194978 MeRIP-seq:(Medium) rs762644377 Functional Loss SNV dbSNP153 33..33 33 - - - 105796 RMVar_ID_105796 Human_SNP_ID_157081943 m1A Human chr3 - 146115352 146115352 146115352 ATCTATTGAGATAGAACACTGACATGTCTGGCAGGGGACTCAGTATGACCACATCAGGTAGAATC ATCTATTGAGATAGAACACTGACATGTCTGGCGGGGGACTCAGTATGACCACATCAGGTAGAATC T C PLOD2 Ensembl:ENSG00000152952 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:146115348..146115576 26863196 MeRIP-seq:(Medium) rs985648043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14661497 RMVar_hsa_circ_64742,RMVar_hsa_circ_67606,RMVar_hsa_circ_54312,RMVar_hsa_circ_352331,RMVar_hsa_circ_71468,RMVar_hsa_circ_357723,RMVar_hsa_circ_12211,RMVar_hsa_circ_286692,RMVar_hsa_circ_288722,RMVar_hsa_circ_222066,RMVar_hsa_circ_26689,RMVar_hsa_circ_355363 105797 RMVar_ID_105797 Human_SNP_ID_157084160 m1A Human chr3 - 146124229 146124229 146124229 AAACCTTCTTTTGTTTCCTTTTGTCTTTGCAGATAAATTATTAGTCATAACTGTAGCAACAAAAG AAACCTTCTTTTGTTTCCTTTTGTCTTTGCAGGTAAATTATTAGTCATAACTGTAGCAACAAAAG T C PLOD2 Ensembl:ENSG00000152952 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:146124201..146124250 26863196 MeRIP-seq:(Medium) rs762959475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9133321 Human_Splice_Rec_493500,Human_Splice_Rec_493501,Human_Splice_Rec_493538,Human_Splice_Rec_493539,Human_Splice_Rec_493574,Human_Splice_Rec_493575,Human_Splice_Rec_493628,Human_Splice_Rec_493629,Human_Splice_Rec_493640,Human_Splice_Rec_493641 Human_miRNA_ID_2921941 GWAS_ID_14554 RMVar_hsa_circ_64742,RMVar_hsa_circ_67606,RMVar_hsa_circ_54312,RMVar_hsa_circ_352331,RMVar_hsa_circ_71468,RMVar_hsa_circ_357723,RMVar_hsa_circ_288722,RMVar_hsa_circ_222066,RMVar_hsa_circ_276696,RMVar_hsa_circ_26689,RMVar_hsa_circ_355363,RMVar_hsa_circ_222067 105798 RMVar_ID_105798 Human_SNP_ID_157092835 m1A Human chr3 - 146160977 146160977 146160977 GCGGCCCTCGAGGGCCGAATATGGGGGGATGCACGGTGAAGCCTCAGCTGCTGCTCCTGGCGCTC GCGGCCCTCGAGGGCCGAATATGGGGGGATGCGCGGTGAAGCCTCAGCTGCTGCTCCTGGCGCTC T C PLOD2 Ensembl:ENSG00000152952 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:146160926..146163603 26863196 MeRIP-seq:(Medium) rs1355371514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784995,Human_RBP_ID_4756776,Human_RBP_ID_5473828 Human_Splice_Rec_493499,Human_Splice_Rec_493537,Human_Splice_Rec_493639 105799 RMVar_ID_105799 Human_SNP_ID_157092845 m1A Human chr3 - 146160989 146160989 146160989 GCCTGAGCCCGCGCGGCCCTCGAGGGCCGAATATGGGGGGATGCACGGTGAAGCCTCAGCTGCTG GCCTGAGCCCGCGCGGCCCTCGAGGGCCGAATGTGGGGGGATGCACGGTGAAGCCTCAGCTGCTG T C PLOD2 Ensembl:ENSG00000152952 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:146160938..146161384;chr3:146160938..146161279 26863196 MeRIP-seq:(Medium) rs1437059258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784995,Human_RBP_ID_4756776,Human_RBP_ID_5473828,Human_RBP_ID_5530699,Human_RBP_ID_24383877 105800 RMVar_ID_105800 Human_SNP_ID_157093580 m1A Human chr3 + 146163587 146163587 146163587 TTACTTCTCTCTTTCCATCCCCCACACCCGCCAACTCACAGAGCCGGACTCCAAATCTTGTCATT TTACTTCTCTCTTTCCATCCCCCACACCCGCCGACTCACAGAGCCGGACTCCAAATCTTGTCATT A G NONHSAG036303.2,lnc-ZIC1-6,lnc-ZIC1-6:2,lnc-ZIC1-6:3,lnc-ZIC1-6:4 RNACentral:URS00008B8F9B,RNACentral:URS0000D5BD49,RNACentral:URS0000D5872D,RNACentral:URS0000D5A1CC,RNACentral:URS0000D5D709 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:146163545..146163693 26863196 MeRIP-seq:(Medium) rs1466423340 Functional Loss SNV dbSNP153 33..33 33 - - - 105801 RMVar_ID_105801 Human_SNP_ID_157186393 m1A Human chr3 + 146544513 146544513 146544513 GTTTCCGCTCCCGAGCGAGACAAGGTCCAGAGAGCCGGGGCCAGGCGATGGCTTCCTCTTCTGCG GTTTCCGCTCCCGAGCGAGACAAGGTCCAGAGCGCCGGGGCCAGGCGATGGCTTCCTCTTCTGCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr3:146541178..146544575;chr3:146544451..146544625 26863196,32194978 MeRIP-seq:(Medium) rs997568310 Functional Loss SNV dbSNP153 33..33 33 - - - 105802 RMVar_ID_105802 Human_SNP_ID_157267302 m1A Human chr3 + 146861440 146861411 146861441 TGATGATGATGGTGATGATGATGATGGTGATGACGATGATGGTGATGATGATGATGATGATGGTG TGAT______________________________GATGATGGTGATGATGATGATGATGATGGTG TGATGATGGTGATGATGATGATGGTGATGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:146861388..146861487 26863196 MeRIP-seq:(Medium) rs1228683655 Functional Loss DEL dbSNP153 5..34 33 - - - 105803 RMVar_ID_105803 Human_SNP_ID_157267308 m1A Human chr3 + 146861440 146861423 146861441 TGATGATGATGGTGATGATGATGATGGTGATGACGATGATGGTGATGATGATGATGATGATGGTG TGATGATGATGGTGAT__________________GATGATGGTGATGATGATGATGATGATGGTG TGATGATGATGGTGATGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:146861388..146861487 26863196 MeRIP-seq:(Medium) rs1461982536 Functional Loss DEL dbSNP153 17..34 33 - - - 105804 RMVar_ID_105804 Human_SNP_ID_157267310 m1A Human chr3 + 146861440 146861426 146861441 TGATGATGATGGTGATGATGATGATGGTGATGACGATGATGGTGATGATGATGATGATGATGGTG TGATGATGATGGTGATGAT_______________GATGATGGTGATGATGATGATGATGATGGTG TGATGATGGTGATGAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:146861388..146861487 26863196 MeRIP-seq:(Medium) rs1469203558 Functional Loss DEL dbSNP153 20..34 33 - - - 105805 RMVar_ID_105805 Human_SNP_ID_157399824 m1A Human chr3 + 147393857 147393847 147393857 CGGTTGCTGGCCCGCGCCTCCCTCCCCGAGGCACCATTGTTCCGGGATCGCTGTGACCGCCACAA CGGTTGCTGGCCCGCGCCTCCCT__________CCATTGTTCCGGGATCGCTGTGACCGCCACAA TCCCCGAGGCA T ZIC1 Ensembl:ENSG00000152977 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:147393719..147393919 32194978 MeRIP-seq:(Medium) rs762441344 Functional Loss DEL dbSNP153 24..33 33 - - - Human_Splice_Rec_494217,Human_Splice_Rec_494219 105806 RMVar_ID_105806 Human_SNP_ID_157791679 m1A Human chr3 + 148991600 148991599 148991600 CTCCCTCCCGGTGCCGGCTTCTCTGAGTCACCAACCTGAGGCTGCCCCGGCCGCCTGCGCACCCG CTCCCTCCCGGTGCCGGCTTCTCTGAGTCACC_ACCTGAGGCTGCCCCGGCCGCCTGCGCACCCG CA C GYG1 Ensembl:ENSG00000163754 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:148991358..148991704 26863196 MeRIP-seq:(Medium) rs770360846 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4726432,Human_RBP_ID_26824173 Human_Splice_Rec_494597,Human_Splice_Rec_494607,Human_Splice_Rec_494619,Human_Splice_Rec_494627,Human_Splice_Rec_494633,Human_Splice_Rec_494647,Human_Splice_Rec_494657,Human_Splice_Rec_494665 105807 RMVar_ID_105807 Human_SNP_ID_157791683 m1A Human chr3 - 148991604 148991604 148991604 CTGCCGGGTGCGCAGGCGGCCGGGGCAGCCTCAGGTTGGTGACTCAGAGAAGCCGGCACCGGGAG CTGCCGGGTGCGCAGGCGGCCGGGGCAGCCTCGGGTTGGTGACTCAGAGAAGCCGGCACCGGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:148991354..148991631 26863196 MeRIP-seq:(Medium) rs1374899287 Functional Loss SNV dbSNP153 33..33 33 - - - 105808 RMVar_ID_105808 Human_SNP_ID_157815407 m1A Human chr3 + 149086423 149086423 149086423 GCCGCCTCGATACGCCTCCTTCCAGGCCCCGCAGCCCTGAAGCCGGGGACAAATTCCGAGCGCCG GCCGCCTCGATACGCCTCCTTCCAGGCCCCGCGGCCCTGAAGCCGGGGACAAATTCCGAGCGCCG A G HLTF-AS1 Ensembl:ENSG00000239718 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:149086373..149086504 26863196 MeRIP-seq:(Medium) rs1430025702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_494937 105809 RMVar_ID_105809 Human_SNP_ID_157826692 m1A Human chr3 - 149129757 149129757 149129757 CGGCTCCAGCTTGCAGGGCACCACCTGCTGCGACCCGAACGGGTGCAGGTTGTACAGCTGCACCA CGGCTCCAGCTTGCAGGGCACCACCTGCTGCGGCCCGAACGGGTGCAGGTTGTACAGCTGCACCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:149129706..149129824 26863196 MeRIP-seq:(Medium) rs779620670 Functional Loss SNV dbSNP153 33..33 33 - - - 105810 RMVar_ID_105810 Human_SNP_ID_157826695 m1A Human chr3 + 149129761 149129761 149129761 GCAGCTGTACAACCTGCACCCGTTCGGGTCGCAGCAGGTGGTGCCCTGCAAGCTGGAGCCGGACC GCAGCTGTACAACCTGCACCCGTTCGGGTCGCCGCAGGTGGTGCCCTGCAAGCTGGAGCCGGACC A C HPS3 Ensembl:ENSG00000163755 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:149129712..149129848 26863196 MeRIP-seq:(Medium) rs746568492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757505 105811 RMVar_ID_105811 Human_SNP_ID_157887452 m1A Human chr3 - 149377472 149377469 149377472 TGGGGCTCGCCCTCCTGTGCATCGCGGCTAATATTTTGCTTTACTTTCCCAATGGGGAAACAAAG TGGGGCTCGCCCTCCTGTGCATCGCGGCTAAT___TTGCTTTACTTTCCCAATGGGGAAACAAAG AAAT A TM4SF1 Ensembl:ENSG00000169908 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:149371746..149377617 32194978 MeRIP-seq:(Medium) rs1360100786 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_70241,Human_RBP_ID_158607,Human_RBP_ID_784721,Human_RBP_ID_4756786,Human_RBP_ID_14664369,Human_RBP_ID_22456317 105812 RMVar_ID_105812 Human_SNP_ID_157887454 m1A Human chr3 - 149377472 149377472 149377472 TGGGGCTCGCCCTCCTGTGCATCGCGGCTAATATTTTGCTTTACTTTCCCAATGGGGAAACAAAG TGGGGCTCGCCCTCCTGTGCATCGCGGCTAATGTTTTGCTTTACTTTCCCAATGGGGAAACAAAG T C TM4SF1 Ensembl:ENSG00000169908 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:149371746..149377617 32194978 MeRIP-seq:(Medium) rs976397753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70241,Human_RBP_ID_158607,Human_RBP_ID_784721,Human_RBP_ID_4756786,Human_RBP_ID_14664369,Human_RBP_ID_22456317 105813 RMVar_ID_105813 Human_SNP_ID_157887692 m1A Human chr3 + 149378378 149378378 149378378 TCAGGAAAAGCAATGCCAGGAAGGGCCAAGGAAGGCCTAAAGCATGGGACAAAAATAAAAAGAGG TCAGGAAAAGCAATGCCAGGAAGGGCCAAGGAGGGCCTAAAGCATGGGACAAAAATAAAAAGAGG A G TM4SF1-AS1 Ensembl:ENSG00000240541 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:149378328..149378695 26863196 MeRIP-seq:(Medium) rs1423686444 Functional Loss SNV dbSNP153 33..33 33 - - - 105814 RMVar_ID_105814 Human_SNP_ID_157887697 m1A Human chr3 + 149378394 149378394 149378394 CAGGAAGGGCCAAGGAAGGCCTAAAGCATGGGACAAAAATAAAAAGAGGAAGAAGAGAGGGGGAG CAGGAAGGGCCAAGGAAGGCCTAAAGCATGGGGCAAAAATAAAAAGAGGAAGAAGAGAGGGGGAG A G TM4SF1-AS1 Ensembl:ENSG00000240541 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:149378344..149378492 26863196 MeRIP-seq:(Medium) rs1249247467 Functional Loss SNV dbSNP153 33..33 33 - - - 105815 RMVar_ID_105815 Human_SNP_ID_157929051 m1A Human chr3 - 149542451 149542451 149542451 ACCACCCCACTCAGAACCCACCCGCAGGGCTCATGAGTATGCCCAATGCGCTGACCACTCAGCAG ACCACCCCACTCAGAACCCACCCGCAGGGCTCCTGAGTATGCCCAATGCGCTGACCACTCAGCAG T G WWTR1 Ensembl:ENSG00000018408 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:149542404..149542572 26863196 MeRIP-seq:(Medium) rs924965978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1031403,Human_RBP_ID_17292509,Human_RBP_ID_19013088 Human_Splice_Rec_495390,Human_Splice_Rec_495402,Human_Splice_Rec_495414,Human_Splice_Rec_495436 RMVar_hsa_circ_25146,RMVar_hsa_circ_310918,RMVar_hsa_circ_52738,RMVar_hsa_circ_222127,RMVar_hsa_circ_222128,RMVar_hsa_circ_124082,RMVar_hsa_circ_324600 105816 RMVar_ID_105816 Human_SNP_ID_157936393 m1A Human chr3 - 149572915 149572915 149572915 CTCTGAATCATATGAACCTCCACCCTGCCGTCAGTTCCACACCAGTGCCTCAGAGGTCCATGGCA CTCTGAATCATATGAACCTCCACCCTGCCGTCCGTTCCACACCAGTGCCTCAGAGGTCCATGGCA T G WWTR1 Ensembl:ENSG00000018408 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:149572822..149572951 26863196 MeRIP-seq:(Medium) rs1332258503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17292510,Human_RBP_ID_19116216 Human_Splice_Rec_495388,Human_Splice_Rec_495389,Human_Splice_Rec_495400,Human_Splice_Rec_495401,Human_Splice_Rec_495412,Human_Splice_Rec_495413,Human_Splice_Rec_495434,Human_Splice_Rec_495435,Human_Splice_Rec_495448 RMVar_hsa_circ_25146,RMVar_hsa_circ_5637,RMVar_hsa_circ_324600,RMVar_hsa_circ_107241,RMVar_hsa_circ_326495,RMVar_hsa_circ_222129,RMVar_hsa_circ_222130 105817 RMVar_ID_105817 Human_SNP_ID_157979144 m1A Human chr3 - 149752422 149752422 149752422 GACAGTGAAGATGCTGCTGGAATTGTCCGAGGAGCATAAGGAACACCTGGCCTTCCTGCCTCAAG GACAGTGAAGATGCTGCTGGAATTGTCCGAGGCGCATAAGGAACACCTGGCCTTCCTGCCTCAAG T G COMMD2 Ensembl:ENSG00000114744 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:149752281..149752443 26863196 MeRIP-seq:(Medium) rs763789500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1619733,Human_RBP_ID_4757508,Human_RBP_ID_8561628,Human_RBP_ID_9394169,Human_RBP_ID_14665900 Human_Splice_Rec_495479,Human_Splice_Rec_495487,Human_Splice_Rec_495503,Human_Splice_Rec_495511,Human_Splice_Rec_495519 RMVar_hsa_circ_106368,RMVar_hsa_circ_222135 105818 RMVar_ID_105818 Human_SNP_ID_157979148 m1A Human chr3 + 149752429 149752429 149752429 CAGGAAGGCCAGGTGTTCCTTATGCTCCTCGGACAATTCCAGCAGCATCTTCACTGTCCTACGAT CAGGAAGGCCAGGTGTTCCTTATGCTCCTCGGCCAATTCCAGCAGCATCTTCACTGTCCTACGAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:149752251..149752461 26863196 MeRIP-seq:(Medium) rs774245187 Functional Loss SNV dbSNP153 33..33 33 - - - 105819 RMVar_ID_105819 Human_SNP_ID_157979151 m1A Human chr3 + 149752440 149752440 149752440 GGTGTTCCTTATGCTCCTCGGACAATTCCAGCAGCATCTTCACTGTCCTACGATTTCACCCGGCA GGTGTTCCTTATGCTCCTCGGACAATTCCAGCCGCATCTTCACTGTCCTACGATTTCACCCGGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:149752276..149752471;chr3:149752284..149752475 26863196 MeRIP-seq:(Medium) rs775575144 Functional Loss SNV dbSNP153 33..33 33 - - - 105820 RMVar_ID_105820 Human_SNP_ID_158030215 m1A Human chr3 - 149970506 149970506 149970506 GGCTGCGCTGACAGGCTGGGGGCGGCGGCCGGACTCCTTGCTGGCCCTGGCCGGGCGCCCCCGGC GGCTGCGCTGACAGGCTGGGGGCGGCGGCCGGGCTCCTTGCTGGCCCTGGCCGGGCGCCCCCGGC T C PFN2 Ensembl:ENSG00000070087 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:149970504..149970627 26863196 MeRIP-seq:(Medium) rs1164457220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18464710,Human_RBP_ID_26763140 105821 RMVar_ID_105821 Human_SNP_ID_158030239 m1A Human chr3 - 149970554 149970554 149970554 TGCCGGGCGGGCGGGGAGGCCGAGGCCCGGGGACGCCCCCTCACCCGGGGCTGCGCTGACAGGCT TGCCGGGCGGGCGGGGAGGCCGAGGCCCGGGGGCGCCCCCTCACCCGGGGCTGCGCTGACAGGCT T C PFN2 Ensembl:ENSG00000070087 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:149970549..149970693 26863196 MeRIP-seq:(Medium) rs1472807723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248104,Human_RBP_ID_785106,Human_RBP_ID_834971,Human_RBP_ID_3722230,Human_RBP_ID_5392232,Human_RBP_ID_18464710,Human_RBP_ID_18953889,Human_RBP_ID_23258671,Human_RBP_ID_26790445 105822 RMVar_ID_105822 Human_SNP_ID_158030406 m1A Human chr3 + 149970923 149970923 149970923 GGAGCAGCAGGCGCAGCGGCGGCGGCGGCGGTAGCGGGCGGCGGCGGCGCGGGGGGAGGCGGGGC GGAGCAGCAGGCGCAGCGGCGGCGGCGGCGGTGGCGGGCGGCGGCGGCGCGGGGGGAGGCGGGGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:149970826..149971075 26863410 MeRIP-seq:(Medium) rs528923379 Functional Loss SNV dbSNP153 33..33 33 - - - 105823 RMVar_ID_105823 Human_SNP_ID_158030501 m1A Human chr3 + 149971084 149971081 149971084 CTCAGAGCGCGCTCGGCCGCCCGGCCGCCCGCAGCCGCGGGGCTGACAAACCAGCGGCGGGAGGC CTCAGAGCGCGCTCGGCCGCCCGGCCGCCC___GCCGCGGGGCTGACAAACCAGCGGCGGGAGGC CGCA C LOC646903 RNACentral:URS00008B8326 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:149971036..149971135 26863196 MeRIP-seq:(Medium) rs936818761 Functional Loss DEL dbSNP153 31..33 33 - - - 105824 RMVar_ID_105824 Human_SNP_ID_158030683 m1A Human chr3 - 149971352 149971352 149971352 GGGGTCCACCCTCTCCGCCGGCCCGAGGTCCGAAGCTCGGCCCGCCACCGCTCCCGGCCGGCGCC GGGGTCCACCCTCTCCGCCGGCCCGAGGTCCGGAGCTCGGCCCGCCACCGCTCCCGGCCGGCGCC T C PFN2 Ensembl:ENSG00000070087 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:149971304..149971406 26863196 MeRIP-seq:(Medium) rs949219258 Functional Loss SNV dbSNP153 33..33 33 - - - 105825 RMVar_ID_105825 Human_SNP_ID_158030684 m1A Human chr3 - 149971352 149971352 149971352 GGGGTCCACCCTCTCCGCCGGCCCGAGGTCCGAAGCTCGGCCCGCCACCGCTCCCGGCCGGCGCC GGGGTCCACCCTCTCCGCCGGCCCGAGGTCCGCAGCTCGGCCCGCCACCGCTCCCGGCCGGCGCC T G PFN2 Ensembl:ENSG00000070087 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:149971304..149971406 26863196 MeRIP-seq:(Medium) rs949219258 Functional Loss SNV dbSNP153 33..33 33 - - - 105826 RMVar_ID_105826 Human_SNP_ID_158030693 m1A Human chr3 - 149971359 149971359 149971359 GCGACGCGGGGTCCACCCTCTCCGCCGGCCCGAGGTCCGAAGCTCGGCCCGCCACCGCTCCCGGC GCGACGCGGGGTCCACCCTCTCCGCCGGCCCGGGGTCCGAAGCTCGGCCCGCCACCGCTCCCGGC T C PFN2 Ensembl:ENSG00000070087 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:149971311..149971414 26863196 MeRIP-seq:(Medium) rs563299541 Functional Loss SNV dbSNP153 33..33 33 - - - 105827 RMVar_ID_105827 Human_SNP_ID_727489336 m1A Human chrX - 106802762 106802762 106802762 CCCGTCTCTTCCCCTCTGCTTCTCCTCCCACCAAATCTTCCTCAGGCGACAGCAGCTCAGGTTCA CCCGTCTCTTCCCCTCTGCTTCTCCTCCCACCTAATCTTCCTCAGGCGACAGCAGCTCAGGTTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chrX:106802711..106802948;chrX:106802711..106802852 26863196 MeRIP-seq:(Medium) rs1340884363 Functional Loss SNV dbSNP153 33..33 33 - - - 105828 RMVar_ID_105828 Human_SNP_ID_727489344 m1A Human chrX - 106802828 106802828 106802828 GCCACATCGCGAACTTTGTGCCCCCCGGGAGCAGTGACCTAGATGCCCTCCTCACCTCACTCTCA GCCACATCGCGAACTTTGTGCCCCCCGGGAGCTGTGACCTAGATGCCCTCCTCACCTCACTCTCA T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:106802730..106802856 26863410 MeRIP-seq:(Medium) rs376292632 Functional Loss SNV dbSNP153 33..33 33 - - - 105829 RMVar_ID_105829 Human_SNP_ID_727489345 m1A Human chrX - 106802828 106802828 106802828 GCCACATCGCGAACTTTGTGCCCCCCGGGAGCAGTGACCTAGATGCCCTCCTCACCTCACTCTCA GCCACATCGCGAACTTTGTGCCCCCCGGGAGCGGTGACCTAGATGCCCTCCTCACCTCACTCTCA T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chrX:106802730..106802856 26863410 MeRIP-seq:(Medium) rs376292632 Functional Loss SNV dbSNP153 33..33 33 - - - 105830 RMVar_ID_105830 Human_SNP_ID_727492096 m1A Human chrX + 106818629 106818624 106818629 GAAGTGATACAGATTTGATTTATCTCTTGTAAAGTCCTTATTTCAACAATCTTTCTATTACAACA GAAGTGATACAGATTTGATTTATCTCTT_____GTCCTTATTTCAACAATCTTTCTATTACAACA TGTAAA T TBC1D8B Ensembl:ENSG00000133138 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:106818620..106818724 26863196 MeRIP-seq:(Medium) rs768130445 Functional Loss DEL dbSNP153 29..33 33 - - - 105831 RMVar_ID_105831 Human_SNP_ID_727513388 m1A Human chrX - 106943200 106943200 106943200 TTACAATTTAATTTCCTCTTCTTGCAGTAAGTACAAATGGATCCTAGGTGAAGAACCGGTGGAGA TTACAATTTAATTTCCTCTTCTTGCAGTAAGTTCAAATGGATCCTAGGTGAAGAACCGGTGGAGA T A MORC4 Ensembl:ENSG00000133131 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:106942981..106954937 32194978 MeRIP-seq:(Medium) rs368894756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_967483 Human_Splice_Rec_2227141,Human_Splice_Rec_2227171 RMVar_hsa_circ_23860,RMVar_hsa_circ_67199,RMVar_hsa_circ_263395,RMVar_hsa_circ_358814,RMVar_hsa_circ_50388 105832 RMVar_ID_105832 Human_SNP_ID_727522852 m1A Human chrX + 106999917 106999917 106999917 CGAAGGCCTGCGGGCCGCCGCCGGGCCGGGCCAGCCCGCAGCCCGGCGCGCCAGGGCCGGCGGGG CGAAGGCCTGCGGGCCGCCGCCGGGCCGGGCCTGCCCGCAGCCCGGCGCGCCAGGGCCGGCGGGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:106999676..107000175 26863410 MeRIP-seq:(Medium) rs770202249 Functional Loss SNV dbSNP153 33..33 33 - - - 105833 RMVar_ID_105833 Human_SNP_ID_727630174 m1A Human chrX - 107650556 107650556 107650556 CACTGTGCTGCCTCCCCCCTCAACCACCCCCCACCCCCCACCCAATGTCTGCTCAAGCTGAGCTG CACTGTGCTGCCTCCCCCCTCAACCACCCCCCCCCCCCCACCCAATGTCTGCTCAAGCTGAGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:107650507..107650603 26863196 MeRIP-seq:(Medium) rs6622249 Functional Loss SNV dbSNP153 33..33 33 - - - 105834 RMVar_ID_105834 Human_SNP_ID_727641392 m1A Human chrX - 107713615 107713615 107713615 CACGGATGCCTTGCTGCTGCAACCCTTTCCCCAGCTGTCCACTGAAACGTGAAGTCCTGTTTTGA CACGGATGCCTTGCTGCTGCAACCCTTTCCCCGGCTGTCCACTGAAACGTGAAGTCCTGTTTTGA T C TSC22D3 Ensembl:ENSG00000157514 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:107713567..107713668 32194978 MeRIP-seq:(Medium) rs1332607230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_725072,Human_RBP_ID_3913281,Human_RBP_ID_5047190,Human_RBP_ID_7964252,Human_RBP_ID_8710737,Human_RBP_ID_9241984,Human_RBP_ID_16786833,Human_RBP_ID_17324366,Human_RBP_ID_18143327,Human_RBP_ID_18401218,Human_RBP_ID_24321649,Human_RBP_ID_27141511,Human_RBP_ID_27549024 Human_miRNA_ID_844893,Human_miRNA_ID_1083921,Human_miRNA_ID_1361346 105835 RMVar_ID_105835 Human_SNP_ID_727642886 m1A Human chrX + 107722242 107722237 107722243 GGAGCCCAAGGAGAATCTTGGTGGAGAGATGGACACTGTCTTGGAAAAGCAGCTCTAGCAATTGA GGAGCCCAAGGAGAATCTTGGTGGAGAG______ACTGTCTTGGAAAAGCAGCTCTAGCAATTGA GATGGAC G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:107722164..107722251 26863410 MeRIP-seq:(Medium) rs1323981747 Functional Loss DEL dbSNP153 29..34 33 - - - 105836 RMVar_ID_105836 Human_SNP_ID_727644636 m1A Human chrX - 107733431 107733431 107733431 TGGGAGAGAAGAAAGGGACAGGCCTAAAGTACACTGGCATTTTTTTTTGTGAAGAGAGCTCTACC TGGGAGAGAAGAAAGGGACAGGCCTAAAGTACGCTGGCATTTTTTTTTGTGAAGAGAGCTCTACC T C TSC22D3 Ensembl:ENSG00000157514 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:107733428..107733506 26863196 MeRIP-seq:(Medium) rs868643185 Functional Loss SNV dbSNP153 33..33 33 - - - 105837 RMVar_ID_105837 Human_SNP_ID_727705851 m1A Human chrX - 108091468 108091468 108091468 CCTAATGGTCTGCAACCTGGCCTACAGCGGGAAGCTGGAAGAGTTGAAGGAGAGTATTCTGGCCG CCTAATGGTCTGCAACCTGGCCTACAGCGGGAGGCTGGAAGAGTTGAAGGAGAGTATTCTGGCCG T C PSMD10 Ensembl:ENSG00000101843 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1327612314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_966985,Human_RBP_ID_1709819,Human_RBP_ID_5076239,Human_RBP_ID_7964425,Human_RBP_ID_18427877,Human_RBP_ID_22467733,Human_RBP_ID_24321798,Human_RBP_ID_27141579 Human_Splice_Rec_2227650,Human_Splice_Rec_2227657,Human_Splice_Rec_2227667,Human_Splice_Rec_2227677,Human_Splice_Rec_2227685,Human_Splice_Rec_2227691,Human_Splice_Rec_2227695 105838 RMVar_ID_105838 Human_SNP_ID_727814814 m1A Human chrX - 108732919 108732919 108732919 CAAGTTGTAGCTGCGGCCTCCGCGCTCGCCGCAGCCCCGGGCATCGGCGCAGCAGCCGCAGCTGC CAAGTTGTAGCTGCGGCCTCCGCGCTCGCCGCGGCCCCGGGCATCGGCGCAGCAGCCGCAGCTGC T C IRS4 Ensembl:ENSG00000133124 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK-293T cells,m1A-IP-seq;HEK293T cell line,total RNA chrX:108732841..108732964 31548705,26863196 m1A-IP-seq:(High) rs373536348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258009,Human_RBP_ID_5047951,Human_RBP_ID_8932008,Human_RBP_ID_27378424 105839 RMVar_ID_105839 Human_SNP_ID_727815631 m1A Human chrX + 108735652 108735652 108735652 CTGGGTTTGACTATTACCTGCCACACATCTTTATAGAAGGGTGGCTCCGCCGCCGCTGCCGCCGC CTGGGTTTGACTATTACCTGCCACACATCTTTGTAGAAGGGTGGCTCCGCCGCCGCTGCCGCCGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:108735551..108735718 26863410 MeRIP-seq:(Medium) rs1193854369 Functional Loss SNV dbSNP153 33..33 33 - - - 105840 RMVar_ID_105840 Human_SNP_ID_727886787 m1A Human chrX - 109054255 109054255 109054255 TTCATCCATTCATGCGCCTCACTAATTAGATGACGAGGCATTTGGCTACCTTAAGAGAGTCATAG TTCATCCATTCATGCGCCTCACTAATTAGATGCCGAGGCATTTGGCTACCTTAAGAGAGTCATAG T G lnc-IRS4-2 RNACentral:URS00008C2C27 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:109054205..109054347 26863196 MeRIP-seq:(Medium) rs1299615144 Functional Loss SNV dbSNP153 33..33 33 - - - 105841 RMVar_ID_105841 Human_SNP_ID_727886822 m1A Human chrX + 109054343 109054343 109054343 ACTATCCAGCGAAACCACAGCCAAGGGAACGGACTTGGCGGAATCAGCGGGGAAAGAAGACTCTG ACTATCCAGCGAAACCACAGCCAAGGGAACGGGCTTGGCGGAATCAGCGGGGAAAGAAGACTCTG A G lnc-COL4A5-3,lnc-COL4A5-3:2 RNACentral:URS00008C3B47,RNACentral:URS0000D5D583 lincRNA,lincRNA exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4893495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1146951,Human_RBP_ID_5048139,Human_RBP_ID_5431765,Human_RBP_ID_5455026,Human_RBP_ID_5482859,Human_RBP_ID_5517023,Human_RBP_ID_7965495,Human_RBP_ID_8161700,Human_RBP_ID_8276834,Human_RBP_ID_8932124,Human_RBP_ID_16789305,Human_RBP_ID_17058095,Human_RBP_ID_17439816,Human_RBP_ID_17552165,Human_RBP_ID_17717433,Human_RBP_ID_18143675,Human_RBP_ID_21957622,Human_RBP_ID_22425007,Human_RBP_ID_23142183,Human_RBP_ID_23317349,Human_RBP_ID_26752898,Human_RBP_ID_27163250,Human_RBP_ID_27549174 105842 RMVar_ID_105842 Human_SNP_ID_727886894 m1A Human chrX + 109054472 109054472 109054472 CCGGCGCCCCCCGGTGTCCCCGCGAGGGGTCCAGGGCGGGGTCTGCCGGCCCTGCGGGCCGCCGG CCGGCGCCCCCCGGTGTCCCCGCGAGGGGTCCGGGGCGGGGTCTGCCGGCCCTGCGGGCCGCCGG A G lnc-COL4A5-3,lnc-COL4A5-3:2,RF02543-057 RNACentral:URS00008C3B47,RNACentral:URS0000D5D583,RNACentral:URS0000990012 lincRNA,lincRNA,rRNA intron,intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:109054422..109054563 26863196 MeRIP-seq:(Medium) rs10871901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271466,Human_RBP_ID_725403,Human_RBP_ID_1120242,Human_RBP_ID_1229005,Human_RBP_ID_1340647,Human_RBP_ID_1404565,Human_RBP_ID_1709956,Human_RBP_ID_3236738,Human_RBP_ID_5078036,Human_RBP_ID_5230654,Human_RBP_ID_5277894,Human_RBP_ID_5431771,Human_RBP_ID_5455030,Human_RBP_ID_5482863,Human_RBP_ID_5517030,Human_RBP_ID_5637328,Human_RBP_ID_8276840,Human_RBP_ID_8711030,Human_RBP_ID_8932132,Human_RBP_ID_9242111,Human_RBP_ID_10446333,Human_RBP_ID_16789311,Human_RBP_ID_17065988,Human_RBP_ID_17070664,Human_RBP_ID_17177882,Human_RBP_ID_17203136,Human_RBP_ID_17324515,Human_RBP_ID_17439819,Human_RBP_ID_17552168,Human_RBP_ID_17717437,Human_RBP_ID_18143681,Human_RBP_ID_18186172,Human_RBP_ID_18521894,Human_RBP_ID_18543825,Human_RBP_ID_21764706,Human_RBP_ID_22518958,Human_RBP_ID_22840483,Human_RBP_ID_23301205,Human_RBP_ID_23317351,Human_RBP_ID_24322352,Human_RBP_ID_24525212,Human_RBP_ID_26568237,Human_RBP_ID_27141883,Human_RBP_ID_27163753,Human_RBP_ID_27549180,Human_RBP_ID_27789251 105843 RMVar_ID_105843 Human_SNP_ID_727991011 m1A Human chrX + 109536945 109536945 109536945 TCATAAGTATTGATCATTCCGCAGCCCTGCGGACCGGACACGTGAGGAGGTAGTGACGCCGACAC TCATAAGTATTGATCATTCCGCAGCCCTGCGGCCCGGACACGTGAGGAGGTAGTGACGCCGACAC A C NXT2 Ensembl:ENSG00000101888 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:109536897..109536980 26863196 MeRIP-seq:(Medium) rs148682193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2228747,Human_Splice_Rec_2228748,Human_Splice_Rec_2228755,Human_Splice_Rec_2228756,Human_Splice_Rec_2228762 105844 RMVar_ID_105844 Human_SNP_ID_728012228 m1A Human chrX + 109658322 109658322 109658322 CTGCTTCACGCCCTCATTACTCACCACCCCCCAGTCTAGGTATCTCCTACAGTCCTCTTCAACTG CTGCTTCACGCCCTCATTACTCACCACCCCCCCGTCTAGGTATCTCCTACAGTCCTCTTCAACTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:109658313..109658413 26863196 MeRIP-seq:(Medium) rs1347122516 Functional Loss SNV dbSNP153 33..33 33 - - - 105845 RMVar_ID_105845 Human_SNP_ID_728018399 m1A Human chrX + 109696195 109696195 109696195 TAAGAAGAACACGAATATCTTCTGTGATTTCAATCTGCAGTAAGAGACAGCATTTATGAGTACAG TAAGAAGAACACGAATATCTTCTGTGATTTCAGTCTGCAGTAAGAGACAGCATTTATGAGTACAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:109696126..109696200 32194978 MeRIP-seq:(Medium) rs1415366677 Functional Loss SNV dbSNP153 33..33 33 - - - 105846 RMVar_ID_105846 Human_SNP_ID_728071054 m1A Human chrX - 110002471 110002471 110002471 TCCTTCCCTTTTCTGCCTCTGGCACTCCCCTCACCCGTCCACCATTCACACCTCCCACCCTCCGC TCCTTCCCTTTTCTGCCTCTGGCACTCCCCTCGCCCGTCCACCATTCACACCTCCCACCCTCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:110002421..110003574;chrX:110002425..110002718 26863196 MeRIP-seq:(Medium) rs1487150674 Functional Loss SNV dbSNP153 33..33 33 - - - 105847 RMVar_ID_105847 Human_SNP_ID_728071060 m1A Human chrX + 110002492 110002491 110002492 TGGTGGACGGGTGAGGGGAGTGCCAGAGGCAGAAAAGGGAAGGAGGCGAGGAGGAGTAGTCGTGG TGGTGGACGGGTGAGGGGAGTGCCAGAGGCAG_AAAGGGAAGGAGGCGAGGAGGAGTAGTCGTGG GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:110002441..110002613 26863196 MeRIP-seq:(Medium) rs1162475229 Functional Loss DEL dbSNP153 33..33 33 - - - 105848 RMVar_ID_105848 Human_SNP_ID_728074347 m1A Human chrX - 110021415 110021415 110021415 ACTCTTCTACTTATCCCCTCCCTTTCCACTGAACTTCCTGGCAATGGGGTAACTGCCTCATTCCA ACTCTTCTACTTATCCCCTCCCTTTCCACTGAGCTTCCTGGCAATGGGGTAACTGCCTCATTCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:110021408..110021580 26863196 MeRIP-seq:(Medium) rs138787162 Functional Loss SNV dbSNP153 33..33 33 - - - 105849 RMVar_ID_105849 Human_SNP_ID_728096891 m1A Human chrX - 110159541 110159541 110159541 ATTTTAACATCCATGCAGGCACCTCTTCCAATACCCTAACCTCGTGGCCTCCTGAACCTCCTCAA ATTTTAACATCCATGCAGGCACCTCTTCCAATGCCCTAACCTCGTGGCCTCCTGAACCTCCTCAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:110159295..110159588 26863196 MeRIP-seq:(Medium) rs778842868 Functional Loss SNV dbSNP153 33..33 33 - - - 105850 RMVar_ID_105850 Human_SNP_ID_728120336 m1A Human chrX + 110317759 110317759 110317759 CGAGGCGGCGGACGATGAGGAGGGTGAGGAAGAGGTGGCGGCGGCCGGGGTAGAAAGTAGGGTCC CGAGGCGGCGGACGATGAGGAGGGTGAGGAAGCGGTGGCGGCGGCCGGGGTAGAAAGTAGGGTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:110317679..110317799 26863196 MeRIP-seq:(Medium) rs967455817 Functional Loss SNV dbSNP153 33..33 33 - - - 105851 RMVar_ID_105851 Human_SNP_ID_728120417 m1A Human chrX + 110317922 110317922 110317922 CCGGTTAGACCTCCCAGCCCGTTGAGCCGCGTACCGGCGCCTCCTAGTCCCAGCTCCCCAGCTCG CCGGTTAGACCTCCCAGCCCGTTGAGCCGCGTGCCGGCGCCTCCTAGTCCCAGCTCCCCAGCTCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:110317874..110318082 26863196 MeRIP-seq:(Medium) rs1448485836 Functional Loss SNV dbSNP153 33..33 33 - - - 105852 RMVar_ID_105852 Human_SNP_ID_728349486 m1A Human chrX - 111619853 111619853 111619853 CTCTAGCCGTGGTCCAGGAGACGGAGGGAACAAAGACCACTGGAAGGAGTCAGATAGGAAAGATG CTCTAGCCGTGGTCCAGGAGACGGAGGGAACAGAGACCACTGGAAGGAGTCAGATAGGAAAGATG T C EIF4BP7 Ensembl:ENSG00000225031 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1314244751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637342,Human_RBP_ID_7966221 105853 RMVar_ID_105853 Human_SNP_ID_728360213 m1A Human chrX - 111681415 111681415 111681415 AGCCAGCTAAGGGGCAGCGGCACCTGTGGTAGAGTTGCGGGGGTTTCTTTCCGAGCGCGACGGTC AGCCAGCTAAGGGGCAGCGGCACCTGTGGTAGGGTTGCGGGGGTTTCTTTCCGAGCGCGACGGTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:111681393..111681538 26863196 MeRIP-seq:(Medium) rs1393970241 Functional Loss SNV dbSNP153 33..33 33 - - - 105854 RMVar_ID_105854 Human_SNP_ID_729048313 m1A Human chrX - 115561220 115561220 115561220 GCAGAGTCCTGGGTCTGGCCCGACTGCCGCCGACCAACCCACTCAGACAACTTCTGCACCTCGGA GCAGAGTCCTGGGTCTGGCCCGACTGCCGCCGCCCAACCCACTCAGACAACTTCTGCACCTCGGA T G PLS3-AS1 Ensembl:ENSG00000271826 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:115561173..115561299 26863196 MeRIP-seq:(Medium) rs957224842 Functional Loss SNV dbSNP153 33..33 33 - - - 105855 RMVar_ID_105855 Human_SNP_ID_729048320 m1A Human chrX + 115561237 115561237 115561237 GTCTGAGTGGGTTGGTCGGCGGCAGTCGGGCCAGACCCAGGACTCTGCGACTTTACGTAAGTGCT GTCTGAGTGGGTTGGTCGGCGGCAGTCGGGCCTGACCCAGGACTCTGCGACTTTACGTAAGTGCT A T PLS3 Ensembl:ENSG00000102024 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:115561136..115561400;chrX:115561151..115561327;chrX:115561151..115561316 26863196 MeRIP-seq:(Medium) rs1367749043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_725996,Human_RBP_ID_5076706,Human_RBP_ID_5277780,Human_RBP_ID_16795990,Human_RBP_ID_18427879,Human_RBP_ID_19149528,Human_RBP_ID_22468463 Human_Splice_Rec_2230816,Human_Splice_Rec_2230826,Human_Splice_Rec_2230856,Human_Splice_Rec_2230860 105856 RMVar_ID_105856 Human_SNP_ID_729055384 m1A Human chrX + 115600820 115600820 115600820 GAGAAAGATCAGTGGGAGGTGGAGTCATTGGGAAACGTGCTTTGGGAGAGGATGAGGCTTCTGAA GAGAAAGATCAGTGGGAGGTGGAGTCATTGGGCAACGTGCTTTGGGAGAGGATGAGGCTTCTGAA A C PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:115600818..115601012 26863196 MeRIP-seq:(Medium) rs1158805405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3238044 105857 RMVar_ID_105857 Human_SNP_ID_729055396 m1A Human chrX - 115600877 115600877 115600877 ACTCTCCTCTATTTTTCCTCTCTCTCTATCCAAATTCTACTCACCCTTCAAGCAAGGTTCAGAAG ACTCTCCTCTATTTTTCCTCTCTCTCTATCCACATTCTACTCACCCTTCAAGCAAGGTTCAGAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:115600875..115601011 26863196 MeRIP-seq:(Medium) rs982370961 Functional Loss SNV dbSNP153 33..33 33 - - - 105858 RMVar_ID_105858 Human_SNP_ID_729087298 m1A Human chrX - 115899714 115899712 115899715 TTGGGCCTGGGGGTGGCTCAAAAGAAAGGAGGAGAGAGAGCACACAGTAGAAAAAGGAAGAGACA TTGGGCCTGGGGGTGGCTCAAAAGAAAGGAG___AGAGAGCACACAGTAGAAAAAGGAAGAGACA TCTC T DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:115899665..115899759 26863196 MeRIP-seq:(Medium) rs1283980984 Functional Loss DEL dbSNP153 32..34 33 - - - 105859 RMVar_ID_105859 Human_SNP_ID_729092559 m1A Human chrX - 115922781 115922781 115922781 AGGGAGTCAAGGAGAAAGAGAGAGAGAGGAAGAGACAGAGGCAAAAGGAAAGTCAAAAAGAGAGA AGGGAGTCAAGGAGAAAGAGAGAGAGAGGAAGCGACAGAGGCAAAAGGAAAGTCAAAAAGAGAGA T G DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:115922735..115922915 26863196 MeRIP-seq:(Medium) rs1246007145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3238239 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 105860 RMVar_ID_105860 Human_SNP_ID_729094931 m1A Human chrX + 115933994 115933994 115933994 TTATTATCTCTTTGAATAAATGTTCTACCCCTATATCTTTCTCTACCTCCTCTTTAAGGCCAATA TTATTATCTCTTTGAATAAATGTTCTACCCCTGTATCTTTCTCTACCTCCTCTTTAAGGCCAATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:115933960..115934128 26863196 MeRIP-seq:(Medium) rs1352622632 Functional Loss SNV dbSNP153 33..33 33 - - - 105861 RMVar_ID_105861 Human_SNP_ID_729101348 m1A Human chrX + 115967704 115967704 115967704 ACCTGTCCCCCTCTGAGGAACCTGTACTACCTACTATTTCCTGACCCATCTTGGTTCTGGCTCCT ACCTGTCCCCCTCTGAGGAACCTGTACTACCTTCTATTTCCTGACCCATCTTGGTTCTGGCTCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:115967661..115967823 26863196 MeRIP-seq:(Medium) rs1012193549 Functional Loss SNV dbSNP153 33..33 33 - - - 105862 RMVar_ID_105862 Human_SNP_ID_729101599 m1A Human chrX + 115969034 115969034 115969034 CTGATCTGCGTTCTGGGGACGGCTGGACCCCAATGCGCCCCCTGCGGCAACGCGACTCCCGCGTT CTGATCTGCGTTCTGGGGACGGCTGGACCCCAGTGCGCCCCCTGCGGCAACGCGACTCCCGCGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:115968989..115969089 26863196 MeRIP-seq:(Medium) rs909280167 Functional Loss SNV dbSNP153 33..33 33 - - - 105863 RMVar_ID_105863 Human_SNP_ID_729539490 m1A Human chrX + 118116656 118116656 118116656 CCGCACCTTCGCACCCTCTGCTCGCCCCGACCACTTCACCCTGTCCTGGCGCAGGCGGAGAGCAC CCGCACCTTCGCACCCTCTGCTCGCCCCGACCGCTTCACCCTGTCCTGGCGCAGGCGGAGAGCAC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:118116501..118116700 26863196 MeRIP-seq:(Medium) rs1319657518 Functional Loss SNV dbSNP153 33..33 33 - - - 105864 RMVar_ID_105864 Human_SNP_ID_729579896 m1A Human chrX + 118346205 118346205 118346205 TGTAGCCGGCGCGCCCTTCTTCCCTTACTGCGAGGAGCCACCGCCTCTTTCGCGCTCCTTATACA TGTAGCCGGCGCGCCCTTCTTCCCTTACTGCGTGGAGCCACCGCCTCTTTCGCGCTCCTTATACA A T WDR44 Ensembl:ENSG00000131725 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:118346156..118346247 26863196 MeRIP-seq:(Medium) rs772071683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257998,Human_RBP_ID_5076248,Human_RBP_ID_5517098 105865 RMVar_ID_105865 Human_SNP_ID_729692370 m1A Human chrX - 118974694 118974694 118974694 AGGAGTGGCAGCTGGAGGAAATCGGGGCAGCCACCGCCGCCATGCCACCGAGCTCCTGACCCTGC AGGAGTGGCAGCTGGAGGAAATCGGGGCAGCCCCCGCCGCCATGCCACCGAGCTCCTGACCCTGC T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:118974651..118974773 26863196 MeRIP-seq:(Medium) rs991830643 Functional Loss SNV dbSNP153 33..33 33 - - - 105866 RMVar_ID_105866 Human_SNP_ID_729692638 m1A Human chrX + 118975433 118975431 118975433 GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAGCAGCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAG__GCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC GCA G LONRF3 Ensembl:ENSG00000175556 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:118975389..118975491 26863196 MeRIP-seq:(Medium) rs1556409078 Functional Loss DEL dbSNP153 32..33 33 - - - 105867 RMVar_ID_105867 Human_SNP_ID_729692639 m1A Human chrX + 118975433 118975433 118975433 GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAGCAGCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAGCCGCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC A C LONRF3 Ensembl:ENSG00000175556 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:118975389..118975491 26863196 MeRIP-seq:(Medium) rs1037145243 Functional Loss SNV dbSNP153 33..33 33 - - - 105868 RMVar_ID_105868 Human_SNP_ID_729695282 m1A Human chrX + 118989526 118989526 118989526 GAAGGGGGATGGTCAGCAGCACCACATGAAAGACCAGGAAGAAGAGGAGGAGAAGTGGGATGCTA GAAGGGGGATGGTCAGCAGCACCACATGAAAGTCCAGGAAGAAGAGGAGGAGAAGTGGGATGCTA A T LONRF3 Ensembl:ENSG00000175556 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:118989475..118989575 26863196 MeRIP-seq:(Medium) rs1348887889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22123256 RMVar_hsa_circ_352356 105869 RMVar_ID_105869 Human_SNP_ID_729740251 m1A Human chrX + 119236809 119236809 119236809 GGCGCCCCTGAGTGGAGGGAGGAATGGCGGCGAGCTAGGGTAGGCGGGTAGGCGGGCAGGCGGAG GGCGCCCCTGAGTGGAGGGAGGAATGGCGGCGGGCTAGGGTAGGCGGGTAGGCGGGCAGGCGGAG A G PGRMC1 Ensembl:ENSG00000101856 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:119236799..119236977 26863196 MeRIP-seq:(Medium) rs1454610839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848907,Human_RBP_ID_8226599 RMVar_hsa_circ_91757,RMVar_hsa_circ_263634 105870 RMVar_ID_105870 Human_SNP_ID_729777705 m1A Human chrX + 119457027 119457026 119457028 AGAGAGAGAAAGAAAGGAAAGAAAGGAAAGAAAGAAAAAAAAGGAAAGAAAGGAAAAGAGAAAGA AGAGAGAGAAAGAAAGGAAAGAAAGGAAAGAA__AAAAAAAAGGAAAGAAAGGAAAAGAGAAAGA AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:119456977..119457065 26863196 MeRIP-seq:(Medium) rs1233667939 Functional Loss DEL dbSNP153 33..34 33 - - - 105871 RMVar_ID_105871 Human_SNP_ID_729778204 m1A Human chrX - 119457299 119457299 119457299 GCCACACTTCTGTGCTTGTTCTTCCCTCTGCCAGGAATGCTCTTCTCCCTCGTTCTTTCTCTCCT GCCACACTTCTGTGCTTGTTCTTCCCTCTGCCGGGAATGCTCTTCTCCCTCGTTCTTTCTCTCCT T C SLC25A5-AS1 RNACentral:URS0000D5C35F lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:119457160..119457509 26863196 MeRIP-seq:(Medium) rs918173270 Functional Loss SNV dbSNP153 33..33 33 - - - 105872 RMVar_ID_105872 Human_SNP_ID_729780385 m1A Human chrX + 119469867 119469867 119469867 AAGCAGATCTTCCTGGGTGGTGTGGACAAGAGAACCCAGTTTTGGCTCTACTTTGCAGGGAATCT AAGCAGATCTTCCTGGGTGGTGTGGACAAGAGGACCCAGTTTTGGCTCTACTTTGCAGGGAATCT A G SLC25A5 Ensembl:ENSG00000005022 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:119469766..119469945 26863196 MeRIP-seq:(Medium) rs73637847 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_726400,Human_RBP_ID_1710341,Human_RBP_ID_2069289,Human_RBP_ID_5049700,Human_RBP_ID_7969131,Human_RBP_ID_8711832,Human_RBP_ID_9242516,Human_RBP_ID_16800789,Human_RBP_ID_18197360,Human_RBP_ID_22468943,Human_RBP_ID_22840582,Human_RBP_ID_24555701,Human_RBP_ID_26835676,Human_RBP_ID_27378817,Human_RBP_ID_27549415 RMVar_hsa_circ_523 105873 RMVar_ID_105873 Human_SNP_ID_729780405 m1A Human chrX - 119469912 119469912 119469912 TACACAAAACACAGGGATGTGGCCCCTGCGGCACCACCCGATGCCAGATTCCCTGCAAAGTAGAG TACACAAAACACAGGGATGTGGCCCCTGCGGCTCCACCCGATGCCAGATTCCCTGCAAAGTAGAG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:119469651..119469975 32194978 MeRIP-seq:(Medium) rs1206050165 Functional Loss SNV dbSNP153 33..33 33 - - - 105874 RMVar_ID_105874 Human_SNP_ID_729800140 m1A Human chrX + 119574698 119574698 119574698 AACCCGAGACCCCAGTGTATGCCCCACCCCTGACCCCGCTCGCGACATGTCCACCCCGGCTCGGC AACCCGAGACCCCAGTGTATGCCCCACCCCTGTCCCCGCTCGCGACATGTCCACCCCGGCTCGGC A T UBE2A Ensembl:ENSG00000077721 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:119574551..119574904 26863196 MeRIP-seq:(Medium) rs1416040436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257857,Human_RBP_ID_800282,Human_RBP_ID_5049785,Human_RBP_ID_9340009,Human_RBP_ID_9410085,Human_RBP_ID_16801662,Human_RBP_ID_24325213 Human_Splice_Rec_2232093,Human_Splice_Rec_2232108,Human_Splice_Rec_2232110,Human_Splice_Rec_2232118,Human_Splice_Rec_2232126,Human_Splice_Rec_2232135,Human_Splice_Rec_2232139 105875 RMVar_ID_105875 Human_SNP_ID_729802826 m1A Human chrX + 119589643 119589643 119589643 TCTCTCTTGGCAATTTTATTCACCCTCTCTACATCCAGACCAAGCCCTTCCCGCTTATGCTGCTC TCTCTCTTGGCAATTTTATTCACCCTCTCTACGTCCAGACCAAGCCCTTCCCGCTTATGCTGCTC A G UBE2A Ensembl:ENSG00000077721 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119589592..119589771 26863196 MeRIP-seq:(Medium) rs757507841 Functional Loss SNV dbSNP153 33..33 33 - - - 105876 RMVar_ID_105876 Human_SNP_ID_729821474 m1A Human chrX - 119693136 119693136 119693136 GTTTCCTGTGCAGTAGCTCCCGTTGCGGCGGCACCCGTGGCAGCCCTGGCGGACGCAGGAGCGAT GTTTCCTGTGCAGTAGCTCCCGTTGCGGCGGCTCCCGTGGCAGCCCTGGCGGACGCAGGAGCGAT T A SEPTIN6 Ensembl:ENSG00000125354 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:119693026..119693177 26863196 MeRIP-seq:(Medium) rs896758856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5076261,Human_RBP_ID_9410088,Human_RBP_ID_18427881 Human_Splice_Rec_2232186,Human_Splice_Rec_2232206,Human_Splice_Rec_2232224,Human_Splice_Rec_2232242,Human_Splice_Rec_2232262,Human_Splice_Rec_2232280,Human_Splice_Rec_2232304 105877 RMVar_ID_105877 Human_SNP_ID_729839061 m1A Human chrX - 119775714 119775714 119775714 AGATCGGGAACTGAAAGTTACTGCATGGCAGGAGTGTAGAAAGGGGATGTATTCGTGGGTGAAGA AGATCGGGAACTGAAAGTTACTGCATGGCAGGGGTGTAGAAAGGGGATGTATTCGTGGGTGAAGA T C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119775676..119775741 26863196 MeRIP-seq:(Medium) rs899340307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16803033 105878 RMVar_ID_105878 Human_SNP_ID_729842131 m1A Human chrX - 119791514 119791514 119791514 GGGGTGGCTTCCCAAAACCCGAGGCCGCTGCCAGGAAATGCCTGGGCCGCGCGGAGCGTTGAGGG GGGGTGGCTTCCCAAAACCCGAGGCCGCTGCCTGGAAATGCCTGGGCCGCGCGGAGCGTTGAGGG T A RPL39 Ensembl:ENSG00000198918 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:119791511..119791615 26863410 MeRIP-seq:(Medium) rs1015582597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369110,Human_RBP_ID_22632248 RMVar_hsa_circ_99384,RMVar_hsa_circ_263663 105879 RMVar_ID_105879 Human_SNP_ID_729842132 m1A Human chrX - 119791514 119791514 119791514 GGGGTGGCTTCCCAAAACCCGAGGCCGCTGCCAGGAAATGCCTGGGCCGCGCGGAGCGTTGAGGG GGGGTGGCTTCCCAAAACCCGAGGCCGCTGCCGGGAAATGCCTGGGCCGCGCGGAGCGTTGAGGG T C RPL39 Ensembl:ENSG00000198918 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:119791511..119791615 26863410 MeRIP-seq:(Medium) rs1015582597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369110,Human_RBP_ID_22632248 RMVar_hsa_circ_99384,RMVar_hsa_circ_263663 105880 RMVar_ID_105880 Human_SNP_ID_729842183 m1A Human chrX + 119791631 119791631 119791631 ACACCACGATGGCGGAGAAAGGAAGAGGAGGGAAGCTGGCGGAAGAACGAGCTTAGAAGGCGCTT ACACCACGATGGCGGAGAAAGGAAGAGGAGGGCAGCTGGCGGAAGAACGAGCTTAGAAGGCGCTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:119791567..119791649;chrX:119791542..119791674;chrX:119791555..119791643 26863196 MeRIP-seq:(Medium) rs917160971 Functional Loss SNV dbSNP153 33..33 33 - - - 105881 RMVar_ID_105881 Human_SNP_ID_729842296 m1A Human chrX - 119792019 119792015 119792019 ATGACTCGTAACCCTCTGGGAAAATGGCACTTACTCTCCGCCTGCCGAGCTCCGACCCGGCGTTC ATGACTCGTAACCCTCTGGGAAAATGGCACTT____TCCGCCTGCCGAGCTCCGACCCGGCGTTC AGAGT A RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119791984..119792050 26863196 MeRIP-seq:(Medium) rs1172942312 Functional Loss DEL dbSNP153 33..36 33 - - - 105882 RMVar_ID_105882 Human_SNP_ID_729842297 m1A Human chrX - 119792019 119792016 119792019 ATGACTCGTAACCCTCTGGGAAAATGGCACTTACTCTCCGCCTGCCGAGCTCCGACCCGGCGTTC ATGACTCGTAACCCTCTGGGAAAATGGCACTT___CTCCGCCTGCCGAGCTCCGACCCGGCGTTC GAGT G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119791984..119792050 26863196 MeRIP-seq:(Medium) rs1478240842 Functional Loss DEL dbSNP153 33..35 33 - - - 105883 RMVar_ID_105883 Human_SNP_ID_729851281 m1A Human chrX - 119841202 119841202 119841202 GAAAGGAGGAGGAGAGAAATAGAAAGAAAAAGACAAAGAGAAGAAGAGAGGAGGAAATGGAAAGA GAAAGGAGGAGGAGAGAAATAGAAAGAAAAAGCCAAAGAGAAGAAGAGAGGAGGAAATGGAAAGA T G UPF3B Ensembl:ENSG00000125351 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:119834824..119843244 26863196 MeRIP-seq:(Medium) rs1030525759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93722,Human_RBP_ID_967517,Human_RBP_ID_5078539,Human_RBP_ID_24549981,Human_RBP_ID_26302595 Human_Splice_Rec_2232352,Human_Splice_Rec_2232372,Human_Splice_Rec_2232397 RMVar_hsa_circ_77325,RMVar_hsa_circ_100356,RMVar_hsa_circ_109896,RMVar_hsa_circ_84898,RMVar_hsa_circ_263666,RMVar_hsa_circ_263667,RMVar_hsa_circ_263668,RMVar_hsa_circ_263665,RMVar_hsa_circ_363361,RMVar_hsa_circ_365099,RMVar_hsa_circ_72356,RMVar_hsa_circ_366896 105884 RMVar_ID_105884 Human_SNP_ID_729853458 m1A Human chrX - 119852367 119852367 119852367 AGAGTGCAGGGTGATTAATGGTACAGGAGGGTAGATCGAGAGCATCCTATTTTGAGAGCAATGGG AGAGTGCAGGGTGATTAATGGTACAGGAGGGTGGATCGAGAGCATCCTATTTTGAGAGCAATGGG T C UPF3B Ensembl:ENSG00000125351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119852364..119852650 26863196 MeRIP-seq:(Medium) rs1264339981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5411452,Human_RBP_ID_16803889 RMVar_hsa_circ_100356,RMVar_hsa_circ_263668 105885 RMVar_ID_105885 Human_SNP_ID_729878864 m1A Human chrX + 119990884 119990880 119990884 CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCACACACACACACACACACACCGCAAGCAGCGGCGA CGTGAGCGCCTGCCAGCAGGGCCTTCCGC____CACACACACACACACACCGCAAGCAGCGGCGA CCACA C RHOXF1P3 Ensembl:ENSG00000282933 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:119990801..119990940 26863410 MeRIP-seq:(Medium) rs5903570 Functional Loss DEL dbSNP153 30..33 33 - - - 105886 RMVar_ID_105886 Human_SNP_ID_729878865 m1A Human chrX + 119990884 119990880 119990884 CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCACACACACACACACACACACCGCAAGCAGCGGCGA CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCA__CACACACACACACACACCGCAAGCAGCGGCGA CCACA CCA RHOXF1P3 Ensembl:ENSG00000282933 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:119990801..119990940 26863410 MeRIP-seq:(Medium) rs5903570 Functional Loss DEL dbSNP153 32..33 33 - - - 105887 RMVar_ID_105887 Human_SNP_ID_729878870 m1A Human chrX + 119990884 119990881 119990884 CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCACACACACACACACACACACCGCAAGCAGCGGCGA CGTGAGCGCCTGCCAGCAGGGCCTTCCGCACACCACACACACACACACACCGCAAGCAGCGGCGA CACA ACAC RHOXF1P3 Ensembl:ENSG00000282933 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:119990801..119990940 26863410 MeRIP-seq:(Medium) rs1555988493 Functional Loss MNV dbSNP153 30..33 33 - - - 105888 RMVar_ID_105888 Human_SNP_ID_729878871 m1A Human chrX + 119990884 119990884 119990884 CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCACACACACACACACACACACCGCAAGCAGCGGCGA CGTGAGCGCCTGCCAGCAGGGCCTTCCGCCACGCACACACACACACACACCGCAAGCAGCGGCGA A G RHOXF1P3 Ensembl:ENSG00000282933 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:119990801..119990940 26863410 MeRIP-seq:(Medium) rs1262178571 Functional Loss SNV dbSNP153 33..33 33 - - - 105889 RMVar_ID_105889 Human_SNP_ID_306601855 m1A Human chr7 + 149415 149415 149415 GGTCCTCCCCCATTGTCTTCCTCGCACCCTCCACTGTTCCCGGCCCTTCACTCTGCGCTTGCGCA GGTCCTCCCCCATTGTCTTCCTCGCACCCTCCGCTGTTCCCGGCCCTTCACTCTGCGCTTGCGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149367..149500 26863196 MeRIP-seq:(Medium) rs972398716 Functional Loss SNV dbSNP153 33..33 33 - - - 105890 RMVar_ID_105890 Human_SNP_ID_306615002 m1A Human chr7 - 188892 188892 188892 CTGTGTGGTGAGGACGAAGGGAGGTCGGCCAGAGCCCCCGGGGAAGGGCTGTTGTCATGTGGATG CTGTGTGGTGAGGACGAAGGGAGGTCGGCCAGTGCCCCCGGGGAAGGGCTGTTGTCATGTGGATG T A AC093627.3 Ensembl:ENSG00000240093 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:188846..188990 26863196 MeRIP-seq:(Medium) rs1233805816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5625986 105891 RMVar_ID_105891 Human_SNP_ID_306616877 m1A Human chr7 + 193543 193528 193543 CCACTCGCTGGAGAAACTGCCGCCCGCGGCCGAGCCGGCCGAGCGCGCCTTGCGGGGGCGGGATC CCACTCGCTGGAGAAACT_______________GCCGGCCGAGCGCGCCTTGCGGGGGCGGGATC TGCCGCCCGCGGCCGA T FAM20C Ensembl:ENSG00000177706 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:193276..193675 26863196 MeRIP-seq:(Medium) rs1183568103 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_22463395 105892 RMVar_ID_105892 Human_SNP_ID_306616884 m1A Human chr7 + 193543 193542 193543 CCACTCGCTGGAGAAACTGCCGCCCGCGGCCGAGCCGGCCGAGCGCGCCTTGCGGGGGCGGGATC CCACTCGCTGGAGAAACTGCCGCCCGCGGCCG_GCCGGCCGAGCGCGCCTTGCGGGGGCGGGATC GA G FAM20C Ensembl:ENSG00000177706 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:193276..193675 26863196 MeRIP-seq:(Medium) rs1562357102 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22463395 105893 RMVar_ID_105893 Human_SNP_ID_306619692 m1A Human chr7 - 202106 202106 202106 GGAACGCTCTCCCCTTCCTGCCACCTGCCCTGAGCACCTCCCACCACTTAACCCACCAACTTTAG GGAACGCTCTCCCCTTCCTGCCACCTGCCCTGGGCACCTCCCACCACTTAACCCACCAACTTTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:202103..202219 26863196 MeRIP-seq:(Medium) rs550207223 Functional Loss SNV dbSNP153 33..33 33 - - - 105894 RMVar_ID_105894 Human_SNP_ID_306619781 m1A Human chr7 + 202348 202348 202348 ATATCTTCCAGTGTGCATAGAGAGAATGGGTGACTGCTGGGTGAGATTGCACTGGGGAATGGGGC ATATCTTCCAGTGTGCATAGAGAGAATGGGTGGCTGCTGGGTGAGATTGCACTGGGGAATGGGGC A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:202344..202710 26863196 MeRIP-seq:(Medium) rs866682185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21042 105895 RMVar_ID_105895 Human_SNP_ID_306619850 m1A Human chr7 + 202564 202564 202564 GACATCTTCCCGTGTGCATAGAGAGGACGGGTAGCTGCTGGGTGGGATTGTACTGGGGAATGGGG GACATCTTCCCGTGTGCATAGAGAGGACGGGTGGCTGCTGGGTGGGATTGTACTGGGGAATGGGG A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:202331..202729 26863196 MeRIP-seq:(Medium) rs1387425481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21042 105896 RMVar_ID_105896 Human_SNP_ID_306620761 m1A Human chr7 + 205321 205321 205321 CGGACACGCACCACCACGACGTCAGCCCCCCGAGTAGCCGGGACCACGGACACGCACCGCCACGA CGGACACGCACCACCACGACGTCAGCCCCCCGGGTAGCCGGGACCACGGACACGCACCGCCACGA A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:205271..205359 26863196 MeRIP-seq:(Medium) rs1463611827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21042 105897 RMVar_ID_105897 Human_SNP_ID_306622104 m1A Human chr7 - 208196 208196 208196 CAACAAACACCAACCTACATTTACACACCCACAGACACCCCCCGACACACCCCTACATACCCCTG CAACAAACACCAACCTACATTTACACACCCACCGACACCCCCCGACACACCCCTACATACCCCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:208194..208302 26863196 MeRIP-seq:(Medium) rs1404884368 Functional Loss SNV dbSNP153 33..33 33 - - - 105898 RMVar_ID_105898 Human_SNP_ID_306624627 m1A Human chr7 + 215118 215118 215118 TACGTGTGTCCAGTCTCCCAAAGTGGCCCAGGAGGACAGGGCGTGGTTAACAGTGGGAGTTATGT TACGTGTGTCCAGTCTCCCAAAGTGGCCCAGGGGGACAGGGCGTGGTTAACAGTGGGAGTTATGT A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:215114..215244 26863196 MeRIP-seq:(Medium) rs989221270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3861050,Human_RBP_ID_8219225,Human_RBP_ID_22703539 RMVar_hsa_circ_307771 105899 RMVar_ID_105899 Human_SNP_ID_306624918 m1A Human chr7 + 216064 216062 216064 GGTGTATGGAGAGGATGGGGCTGGGTGGGGGGAGCAGGGCCCCTGGTGTATGGAGAGGATGGAGC GGTGTATGGAGAGGATGGGGCTGGGTGGGGG__GCAGGGCCCCTGGTGTATGGAGAGGATGGAGC GGA G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:216059..216262 26863196 MeRIP-seq:(Medium) rs1211477262 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_307771 105900 RMVar_ID_105900 Human_SNP_ID_306624957 m1A Human chr7 + 216235 216233 216235 CCCCTGGTGTATGGAGAGGATGGGGCTGGGTGAGGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT CCCCTGGTGTATGGAGAGGATGGGGCTGGGT__GGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT TGA T FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:216059..216262 26863196 MeRIP-seq:(Medium) rs1357978227 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_307771 105901 RMVar_ID_105901 Human_SNP_ID_306624958 m1A Human chr7 + 216235 216235 216235 CCCCTGGTGTATGGAGAGGATGGGGCTGGGTGAGGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT CCCCTGGTGTATGGAGAGGATGGGGCTGGGTGGGGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:216059..216262 26863196 MeRIP-seq:(Medium) rs28603028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307771 105902 RMVar_ID_105902 Human_SNP_ID_306624959 m1A Human chr7 + 216235 216235 216235 CCCCTGGTGTATGGAGAGGATGGGGCTGGGTGAGGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT CCCCTGGTGTATGGAGAGGATGGGGCTGGGTGTGGGGAGCAGGGCCCGTGGTGTATGGAGAGGAT A T FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:216059..216262 26863196 MeRIP-seq:(Medium) rs28603028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307771 105903 RMVar_ID_105903 Human_SNP_ID_306626954 m1A Human chr7 + 222109 222066 222109 CAGGAGCCGTTCTTAGCATCTGGGCACCCGGGAGGGAGGGGCCTGTGGGGAGCCAGAAGTGCGCA _________________________________GGGAGGGGCCTGTGGGGAGCCAGAAGTGCGCA GCAGGGGGCTGCAGGAGCCGTTCTTAGCATCTGGGCACCCGGGA G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:222105..222358 26863196 MeRIP-seq:(Medium) rs1394313258 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_3861093,Human_RBP_ID_22729609 RMVar_hsa_circ_307771 105904 RMVar_ID_105904 Human_SNP_ID_306626974 m1A Human chr7 + 222109 222109 222109 CAGGAGCCGTTCTTAGCATCTGGGCACCCGGGAGGGAGGGGCCTGTGGGGAGCCAGAAGTGCGCA CAGGAGCCGTTCTTAGCATCTGGGCACCCGGGGGGGAGGGGCCTGTGGGGAGCCAGAAGTGCGCA A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:222105..222358 26863196 MeRIP-seq:(Medium) rs1425367146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3861093,Human_RBP_ID_22729609 RMVar_hsa_circ_307771 105905 RMVar_ID_105905 Human_SNP_ID_306631880 m1A Human chr7 - 236819 236808 236820 CACCCGCCTCACCTCCGCATGAAACCCCGACCATAACCCCGACAGCCACCGGGACCCCAGATTCC CACCCGCCTCACCTCCGCATGAAACCCCGAC____________AGCCACCGGGACCCCAGATTCC TGTCGGGGTTATG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:236665..236924 26863196 MeRIP-seq:(Medium) rs1415032180 Functional Loss DEL dbSNP153 32..43 33 - - - 105906 RMVar_ID_105906 Human_SNP_ID_306632137 m1A Human chr7 + 237772 237772 237772 AGATGATGATAATGATGATGATGGTGATGGTGATGATGATGTTGATAAGGATGATAATGATGGTG AGATGATGATAATGATGATGATGGTGATGGTGGTGATGATGTTGATAAGGATGATAATGATGGTG A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:237445..237818;chr7:237454..237819 26863196 MeRIP-seq:(Medium) rs1487962567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842378,Human_RBP_ID_17169956 RMVar_hsa_circ_307771 105907 RMVar_ID_105907 Human_SNP_ID_306632155 m1A Human chr7 + 240328 240328 240328 GGTAATAGTGATAGTGATGATGATGGTGGTGGAGGTGATGATTATGATGTTGATAAAGGATGATA GGTAATAGTGATAGTGATGATGATGGTGGTGGTGGTGATGATTATGATGTTGATAAAGGATGATA A T FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:240279..240600 26863196 MeRIP-seq:(Medium) rs1477435178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842333,Human_RBP_ID_17169957 RMVar_hsa_circ_307771 105908 RMVar_ID_105908 Human_SNP_ID_306640950 m1A Human chr7 + 263236 263236 263236 CAGCGGGCACAGGACAGAGAAGAGGAAGCCGCAGCAGCCCCAGTGCCGACCAGCAGCGGGCACAG CAGCGGGCACAGGACAGAGAAGAGGAAGCCGCTGCAGCCCCAGTGCCGACCAGCAGCGGGCACAG A T lnc-FAM20C-8 RNACentral:URS00009B9D48 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:263185..263273 26863196 MeRIP-seq:(Medium) rs74190809 Functional Loss SNV dbSNP153 33..33 33 - - - 105909 RMVar_ID_105909 Human_SNP_ID_306641212 m1A Human chr7 + 264031 264031 264031 CAGCGGGCACAGGACAGAGAAGAGGAAGCGGCAGCAGCCCCAGCGCCGACCAGCAGCGGGCACAG CAGCGGGCACAGGACAGAGAAGAGGAAGCGGCTGCAGCCCCAGCGCCGACCAGCAGCGGGCACAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:263975..264098 26863196 MeRIP-seq:(Medium) rs373377469 Functional Loss SNV dbSNP153 33..33 33 - - - 105910 RMVar_ID_105910 Human_SNP_ID_306673380 m1A Human chr7 + 356039 356031 356040 TCATCATCATCATCATCATCATCATCACCACCACCATCACCACCATCACCATCACCATCATCACC TCATCATCATCATCATCATCATCAT_________CATCACCACCATCACCATCACCATCATCACC TCACCACCAC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:355908..356081 26863196 MeRIP-seq:(Medium) rs1562437025 Functional Loss DEL dbSNP153 26..34 33 - - - 105911 RMVar_ID_105911 Human_SNP_ID_306673381 m1A Human chr7 + 356039 356031 356040 TCATCATCATCATCATCATCATCATCACCACCACCATCACCACCATCACCATCACCATCATCACC TCATCATCATCATCATCATCATCATCAC______CATCACCACCATCACCATCACCATCATCACC TCACCACCAC TCAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:355908..356081 26863196 MeRIP-seq:(Medium) rs1562437025 Functional Loss DEL dbSNP153 29..34 33 - - - 105912 RMVar_ID_105912 Human_SNP_ID_306673382 m1A Human chr7 + 356039 356031 356040 TCATCATCATCATCATCATCATCATCACCACCACCATCACCACCATCACCATCACCATCATCACC TCATCATCATCATCATCATCATCATCACCAC___CATCACCACCATCACCATCACCATCATCACC TCACCACCAC TCACCAC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:355908..356081 26863196 MeRIP-seq:(Medium) rs1562437025 Functional Loss DEL dbSNP153 32..34 33 - - - 105913 RMVar_ID_105913 Human_SNP_ID_306673436 m1A Human chr7 + 356081 356067 356082 CCATCACCATCACCATCATCACCATCACCATCACCACCATCACCATCACCACCATCAGCATCACC CCATCACCATCACCATCAT_______________CACCATCACCATCACCACCATCAGCATCACC TCACCATCACCATCAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:355997..356081 26863196 MeRIP-seq:(Medium) rs1387301676 Functional Loss DEL dbSNP153 20..34 33 - - - 105914 RMVar_ID_105914 Human_SNP_ID_306673449 m1A Human chr7 + 356081 356079 356082 CCATCACCATCACCATCATCACCATCACCATCACCACCATCACCATCACCACCATCAGCATCACC CCATCACCATCACCATCATCACCATCACCAT___CACCATCACCATCACCACCATCAGCATCACC TCAC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:355997..356081 26863196 MeRIP-seq:(Medium) rs1294170550 Functional Loss DEL dbSNP153 32..34 33 - - - 105915 RMVar_ID_105915 Human_SNP_ID_306705644 m1A Human chr7 + 454422 454422 454422 ACTCCAAGTCAGAATTCTCTCCAGGGGTCCACACGGCCACCTGAGGAAGGGGTAACAATTCCTGC ACTCCAAGTCAGAATTCTCTCCAGGGGTCCACTCGGCCACCTGAGGAAGGGGTAACAATTCCTGC A T HSALNG0055535 RNACentral:URS0000EB9EFC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:454375..454545 26863196 MeRIP-seq:(Medium) rs538295877 Functional Loss SNV dbSNP153 33..33 33 - - - 105916 RMVar_ID_105916 Human_SNP_ID_306706516 m1A Human chr7 + 456232 456232 456232 CCCAGGCCTCCCACCCCAACGCCGGGACCCCCAGGTCTCCCACTCCGGACCTCCCACTCCAACGC CCCAGGCCTCCCACCCCAACGCCGGGACCCCCGGGTCTCCCACTCCGGACCTCCCACTCCAACGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:456176..456300 26863196 MeRIP-seq:(Medium) rs1368000475 Functional Loss SNV dbSNP153 33..33 33 - - - 105917 RMVar_ID_105917 Human_SNP_ID_306706582 m1A Human chr7 + 456376 456376 456376 CCAGGCCTCCCACCCCAACGCCAGGACCCCAGATCTCCCACTCCGGACCTCCCACTCCAACGCTG CCAGGCCTCCCACCCCAACGCCAGGACCCCAGGTCTCCCACTCCGGACCTCCCACTCCAACGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:456326..456425 26863196 MeRIP-seq:(Medium) rs1407838926 Functional Loss SNV dbSNP153 33..33 33 - - - 105918 RMVar_ID_105918 Human_SNP_ID_306706799 m1A Human chr7 + 456989 456989 456989 CAACGCCAGGACCCCCAGATCTCCCACCCTGGACCTCCTACTCCAACGCTGGGACCCCCGGGCCT CAACGCCAGGACCCCCAGATCTCCCACCCTGGGCCTCCTACTCCAACGCTGGGACCCCCGGGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:456876..457300 26863196 MeRIP-seq:(Medium) rs1020098004 Functional Loss SNV dbSNP153 33..33 33 - - - 105919 RMVar_ID_105919 Human_SNP_ID_306710325 m1A Human chr7 - 466691 466691 466691 AGGAGAAAGGTGAAGGATGACAGTAAGGGATGAGGGTGAGGGAGGAGAGTGAAGGAGGAGGGTGA AGGAGAAAGGTGAAGGATGACAGTAAGGGATGGGGGTGAGGGAGGAGAGTGAAGGAGGAGGGTGA T C HSALNG0055536 RNACentral:URS0000E9C789 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:466682..466784 26863196 MeRIP-seq:(Medium) rs1454330081 Functional Loss SNV dbSNP153 33..33 33 - - - 105920 RMVar_ID_105920 Human_SNP_ID_306710742 m1A Human chr7 + 467584 467584 467584 ACCTCCTCCCAAAACCATCACCTCCCATGGCCATCACCTCGTCCCACAACCGTCACCACCCATGA ACCTCCTCCCAAAACCATCACCTCCCATGGCCCTCACCTCGTCCCACAACCGTCACCACCCATGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:467582..467659 26863196 MeRIP-seq:(Medium) rs534944275 Functional Loss SNV dbSNP153 33..33 33 - - - 105921 RMVar_ID_105921 Human_SNP_ID_306721751 m1A Human chr7 - 500877 500877 500877 CCAAGCTGCGGCACTGGCAGGAGAGGAGATTCAGGTCTCACTGAGAGGGGCTGGGAGTGCATAAG CCAAGCTGCGGCACTGGCAGGAGAGGAGATTCTGGTCTCACTGAGAGGGGCTGGGAGTGCATAAG T A PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:500873..501072 32194978 MeRIP-seq:(Medium) rs749313581 Functional Loss SNV dbSNP153 33..33 33 - - - 105922 RMVar_ID_105922 Human_SNP_ID_306727454 m1A Human chr7 + 517405 517405 517405 GAGGGAAGGGGCGCGATTTACCTACGGAGTCTATCTCCAGGAGTCGCTGGAGGTCCCGGATGCTG GAGGGAAGGGGCGCGATTTACCTACGGAGTCTGTCTCCAGGAGTCGCTGGAGGTCCCGGATGCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:517399..518427 32194978 MeRIP-seq:(Medium) rs1287227282 Functional Loss SNV dbSNP153 33..33 33 - - - 105923 RMVar_ID_105923 Human_SNP_ID_306727995 m1A Human chr7 + 519059 519059 519059 GAGGAGAGGCGAGGCCGCGGGGCGGGCGCTCCAGCCGGTCTCCTGTGGCGGCGAAATTCAGTACC GAGGAGAGGCGAGGCCGCGGGGCGGGCGCTCCGGCCGGTCTCCTGTGGCGGCGAAATTCAGTACC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:519009..519217 26863196 MeRIP-seq:(Medium) rs890265689 Functional Loss SNV dbSNP153 33..33 33 - - - 105924 RMVar_ID_105924 Human_SNP_ID_306728276 m1A Human chr7 - 519896 519896 519896 GCGGGGGGGGGGGGCGGGGGCGGGGGCGGGGGAGGGGCGCGGCGGCGGCGCTATAACCCTCTCCC GCGGGGGGGGGGGGCGGGGGCGGGGGCGGGGGGGGGGCGCGGCGGCGGCGCTATAACCCTCTCCC T C PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:519876..519950 26863196 MeRIP-seq:(Medium) rs181355675 Functional Loss SNV dbSNP153 33..33 33 - - - 105925 RMVar_ID_105925 Human_SNP_ID_306728277 m1A Human chr7 - 519896 519896 519896 GCGGGGGGGGGGGGCGGGGGCGGGGGCGGGGGAGGGGCGCGGCGGCGGCGCTATAACCCTCTCCC GCGGGGGGGGGGGGCGGGGGCGGGGGCGGGGGCGGGGCGCGGCGGCGGCGCTATAACCCTCTCCC T G PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:519876..519950 26863196 MeRIP-seq:(Medium) rs181355675 Functional Loss SNV dbSNP153 33..33 33 - - - 105926 RMVar_ID_105926 Human_SNP_ID_306728322 m1A Human chr7 - 519930 519917 519930 GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGGAGGCGGGGGGGGGGGGCGGGGGCGGGGGCGGGG GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGG_____________GGGCGGGGGCGGGGGCGGGG CCCCCCCCCCGCCT C PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:519876..520019;chr7:519876..519950 26863196 MeRIP-seq:(Medium) rs1209956333 Functional Loss DEL dbSNP153 33..45 33 - - - 105927 RMVar_ID_105927 Human_SNP_ID_306728334 m1A Human chr7 - 519930 519926 519930 GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGGAGGCGGGGGGGGGGGGCGGGGGCGGGGGCGGGG GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGG____GGGGGGGGGGGGCGGGGGCGGGGGCGGGG CGCCT C PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:519876..520019;chr7:519876..519950 26863196 MeRIP-seq:(Medium) rs1292691728 Functional Loss DEL dbSNP153 33..36 33 - - - 105928 RMVar_ID_105928 Human_SNP_ID_306728340 m1A Human chr7 - 519930 519930 519930 GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGGAGGCGGGGGGGGGGGGCGGGGGCGGGGGCGGGG GAGGTGCGGGTCCCAGGCCCGGAATCCGGGGGGGGCGGGGGGGGGGGGCGGGGGCGGGGGCGGGG T C PDGFA Ensembl:ENSG00000197461 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:519876..520019;chr7:519876..519950 26863196 MeRIP-seq:(Medium) rs747292548 Functional Loss SNV dbSNP153 33..33 33 - - - 105929 RMVar_ID_105929 Human_SNP_ID_306729155 m1A Human chr7 - 522368 522368 522368 GGGCGGGGCAGGTGCCGCAGCCTCCGCGCGCAAAACCCGCCGGCGGGGCCCGGGTCGCACCGTCC GGGCGGGGCAGGTGCCGCAGCCTCCGCGCGCAGAACCCGCCGGCGGGGCCCGGGTCGCACCGTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:522352..522461 26863196 MeRIP-seq:(Medium) rs1343027466 Functional Loss SNV dbSNP153 33..33 33 - - - 105930 RMVar_ID_105930 Human_SNP_ID_306741111 m1A Human chr7 + 549954 549954 549954 TTTGCGGGAGGGGCCTTGACTTCTTCGGCCTCAACTCCCTGCTCTCAGCCTCATCTCCCCTGGGG TTTGCGGGAGGGGCCTTGACTTCTTCGGCCTCGACTCCCTGCTCTCAGCCTCATCTCCCCTGGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:549841..549995 26863196 MeRIP-seq:(Medium) rs1323006780 Functional Loss SNV dbSNP153 33..33 33 - - - 105931 RMVar_ID_105931 Human_SNP_ID_306741223 m1A Human chr7 - 550214 550214 550214 AATCAAAGGACAAGCGGACAAAATGCATCCCAAGATCAAGGAAGGGACAGGCCAGCTTCCTCCCC AATCAAAGGACAAGCGGACAAAATGCATCCCATGATCAAGGAAGGGACAGGCCAGCTTCCTCCCC T A PRKAR1B Ensembl:ENSG00000188191 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:550134..550341 26863196 MeRIP-seq:(Medium) rs1482253775 Functional Loss SNV dbSNP153 33..33 33 - - - 105932 RMVar_ID_105932 Human_SNP_ID_306741251 m1A Human chr7 - 550286 550286 550286 TCCCGGCAGCGTGAGGACTGCCCCTTCCCCGGACTCACTTTTTGGAATAAATGATCACCTTGTGC TCCCGGCAGCGTGAGGACTGCCCCTTCCCCGGCCTCACTTTTTGGAATAAATGATCACCTTGTGC T G PRKAR1B Ensembl:ENSG00000188191 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:550238..550321 26863196 MeRIP-seq:(Medium) rs1199934475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17665189,Human_RBP_ID_26550235 Human_miRNA_ID_867744 105933 RMVar_ID_105933 Human_SNP_ID_306741766 m1A Human chr7 - 551472 551472 551472 GCTGGCACTCACGTCTGTCCACCTCCACCCACAGGGCACCGCGTCCGTGCTGCAGCGCCGGTCCC GCTGGCACTCACGTCTGTCCACCTCCACCCACGGGGCACCGCGTCCGTGCTGCAGCGCCGGTCCC T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:551429..602569 26863196 MeRIP-seq:(Medium) rs1292714367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_836191,Human_Splice_Rec_836211,Human_Splice_Rec_836231,Human_Splice_Rec_836251,Human_Splice_Rec_836271,Human_Splice_Rec_836281 RMVar_hsa_circ_267663 105934 RMVar_ID_105934 Human_SNP_ID_306747121 m1A Human chr7 + 566568 566568 566568 ACCACCATCACCATCATTGTCATCACCTTCACATCACCATTACCACCATTACCTTCATCACCATT ACCACCATCACCATCATTGTCATCACCTTCACCTCACCATTACCACCATTACCTTCATCACCATT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:566561..566674 26863196 MeRIP-seq:(Medium) rs1467966240 Functional Loss SNV dbSNP153 33..33 33 - - - 105935 RMVar_ID_105935 Human_SNP_ID_306747122 m1A Human chr7 + 566568 566568 566568 ACCACCATCACCATCATTGTCATCACCTTCACATCACCATTACCACCATTACCTTCATCACCATT ACCACCATCACCATCATTGTCATCACCTTCACGTCACCATTACCACCATTACCTTCATCACCATT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:566561..566674 26863196 MeRIP-seq:(Medium) rs1467966240 Functional Loss SNV dbSNP153 33..33 33 - - - 105936 RMVar_ID_105936 Human_SNP_ID_306750686 m1A Human chr7 - 576974 576974 576974 GAGTTGGATGAGGCCGCTGATGGCGTTGGACGAGGCCGCTGATGGCGTTGGAAGATGCTCACCAC GAGTTGGATGAGGCCGCTGATGGCGTTGGACGGGGCCGCTGATGGCGTTGGAAGATGCTCACCAC T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:576886..577128 26863196 MeRIP-seq:(Medium) rs181752130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22728952 RMVar_hsa_circ_267663 105937 RMVar_ID_105937 Human_SNP_ID_306753169 m1A Human chr7 - 583466 583443 583467 GTGCACACACGTGTGTGCGTGGGTGTGAGTGCACGTGTGTGAGTGGGTGTGAGTGTGCACTGTGG GTGCACACACGTGTGTGCGTGGGTGTGAGTG________________________TGCACTGTGG ACACTCACACCCACTCACACACGTG A PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:583371..583512 26863196 MeRIP-seq:(Medium) rs1381095315 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_5305740,Human_RBP_ID_9354799,Human_RBP_ID_17315067 RMVar_hsa_circ_109563,RMVar_hsa_circ_267663,RMVar_hsa_circ_290376,RMVar_hsa_circ_302771,RMVar_hsa_circ_342825,RMVar_hsa_circ_276511,RMVar_hsa_circ_243184,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_243185,RMVar_hsa_circ_243183 105938 RMVar_ID_105938 Human_SNP_ID_306755194 m1A Human chr7 - 588733 588689 588734 CCACCATCACCATCACCATCACCACTGTCACTATCCTCACCACCATCACCACCATCACCATCACC CCACCATCACCATCACCATCACCACTGTCAC__________________________________ GATGGTGGTGATGGTGATGGTGATGGTGGTGATGGTGGTGAGGATA G PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:588731..589037 26863196 MeRIP-seq:(Medium) rs1442860961 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_13819,RMVar_hsa_circ_109563,RMVar_hsa_circ_302771,RMVar_hsa_circ_342825,RMVar_hsa_circ_276511,RMVar_hsa_circ_243184,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_243185,RMVar_hsa_circ_337394 105939 RMVar_ID_105939 Human_SNP_ID_306760903 m1A Human chr7 + 606235 606235 606235 CCTTGATCAACGACATAGAAGTTGTCTCCTTCATTCCCTGTAACAAAAGAAGAAAGTCAACAGAT CCTTGATCAACGACATAGAAGTTGTCTCCTTCGTTCCCTGTAACAAAAGAAGAAAGTCAACAGAT A G PRKAR1B-AS1 Ensembl:ENSG00000237181 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:606227..677254 26863196 MeRIP-seq:(Medium) rs1177730178 Functional Loss SNV dbSNP153 33..33 33 - - - 105940 RMVar_ID_105940 Human_SNP_ID_306769990 m1A Human chr7 - 636396 636324 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTG_________________________________ ACACGTCCTCCACCGGCCGCGCCCACACGTCCTCCACCGGCCGCGCCCACACGTCCTCCACCGGCCGCGCCCT A PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs1562579076 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105941 RMVar_ID_105941 Human_SNP_ID_306770040 m1A Human chr7 - 636396 636372 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTG________________________TGGGCGCGG ACACGTCCTCCACCGGCCGCGCCCT A PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs1562579213 Functional Loss DEL dbSNP153 33..56 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105942 RMVar_ID_105942 Human_SNP_ID_306770054 m1A Human chr7 - 636396 636384 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTG____________GTGGAGGACGTGTGGGCGCGG CCGGCCGCGCCCT C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs1341540835 Functional Loss DEL dbSNP153 33..44 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105943 RMVar_ID_105943 Human_SNP_ID_306770057 m1A Human chr7 - 636396 636387 636397 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGT__________CCGGTGGAGGACGTGTGGGCGCGG GCCGCGCCCTC G PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs1562579251 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105944 RMVar_ID_105944 Human_SNP_ID_306770064 m1A Human chr7 - 636396 636394 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTG__GGCGCGGCCGGTGGAGGACGTGTGGGCGCGG CCT C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs1217568437 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105945 RMVar_ID_105945 Human_SNP_ID_306770066 m1A Human chr7 - 636396 636396 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG T A PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs371463941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105946 RMVar_ID_105946 Human_SNP_ID_306770067 m1A Human chr7 - 636396 636396 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGGGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs371463941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105947 RMVar_ID_105947 Human_SNP_ID_306770068 m1A Human chr7 - 636396 636396 636396 AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGAGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG AGGACGTGTGGGCGCGGCCGGTGGAGGACGTGCGGGCGCGGCCGGTGGAGGACGTGTGGGCGCGG T G PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:636386..636502 26863196 MeRIP-seq:(Medium) rs371463941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105948 RMVar_ID_105948 Human_SNP_ID_306776999 m1A Human chr7 + 660442 660442 660442 ACCTACTCTCCCCCCAGTGCCACAGGCTCCCCACCCCAACGGGTCCAAATACCTACTCTGCCCCC ACCTACTCTCCCCCCAGTGCCACAGGCTCCCCCCCCCAACGGGTCCAAATACCTACTCTGCCCCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:660418..660547 26863196 MeRIP-seq:(Medium) rs1272394455 Functional Loss SNV dbSNP153 33..33 33 - - - 105949 RMVar_ID_105949 Human_SNP_ID_306777986 m1A Human chr7 - 662686 662686 662686 TGGATCTGTTGGGGTGGGGACCTGTGCCACTGAGGGGAGAGTAGGTATTTGGATCTGTTGGAGTG TGGATCTGTTGGGGTGGGGACCTGTGCCACTGGGGGGAGAGTAGGTATTTGGATCTGTTGGAGTG T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:662634..662815 26863196 MeRIP-seq:(Medium) rs1396147407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3098943,Human_RBP_ID_8217311,Human_RBP_ID_22418897,Human_RBP_ID_26794110 RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783 105950 RMVar_ID_105950 Human_SNP_ID_306783344 m1A Human chr7 + 680681 680681 680681 GGTGGGCGACACCTCCTCATCATGGGAGTCCGACTGTGAGTTTGACTTTTGCCGCGCCAAAATCT GGTGGGCGACACCTCCTCATCATGGGAGTCCGGCTGTGAGTTTGACTTTTGCCGCGCCAAAATCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:680511..691552 26863196 MeRIP-seq:(Medium) rs1379696670 Functional Loss SNV dbSNP153 33..33 33 - - - 105951 RMVar_ID_105951 Human_SNP_ID_306783350 m1A Human chr7 - 680691 680691 680691 GAAAACAGGCAGATTTTGGCGCGGCAAAAGTCAAACTCACAGTCGGACTCCCATGATGAGGAGGT GAAAACAGGCAGATTTTGGCGCGGCAAAAGTCCAACTCACAGTCGGACTCCCATGATGAGGAGGT T G PRKAR1B Ensembl:ENSG00000188191 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:680588..691552 26863196 MeRIP-seq:(Medium) rs781027465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18103667 Human_Splice_Rec_836176,Human_Splice_Rec_836196,Human_Splice_Rec_836216,Human_Splice_Rec_836236,Human_Splice_Rec_836256,Human_Splice_Rec_836286,Human_Splice_Rec_836300,Human_Splice_Rec_836312,Human_Splice_Rec_836320 RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_85211,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783,RMVar_hsa_circ_288369,RMVar_hsa_circ_271059,RMVar_hsa_circ_243194,RMVar_hsa_circ_243195,RMVar_hsa_circ_243193 105952 RMVar_ID_105952 Human_SNP_ID_306793022 m1A Human chr7 - 711477 711477 711477 CGCCATGGCCTCCCCGCCCGCCTGCCCCTCGGAGGAGGACGAGAGCCTGAAGGGCTGTGAGCTGT CGCCATGGCCTCCCCGCCCGCCTGCCCCTCGGGGGAGGACGAGAGCCTGAAGGGCTGTGAGCTGT T C PRKAR1B Ensembl:ENSG00000188191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:711426..712430 26863196 MeRIP-seq:(Medium) rs770920851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956098,Human_RBP_ID_26356108 Human_Splice_Rec_836174,Human_Splice_Rec_836194,Human_Splice_Rec_836214,Human_Splice_Rec_836234,Human_Splice_Rec_836254,Human_Splice_Rec_836284,Human_Splice_Rec_836310,Human_Splice_Rec_836318,Human_Splice_Rec_836322 RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_85211,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783,RMVar_hsa_circ_271059,RMVar_hsa_circ_243194,RMVar_hsa_circ_243198,RMVar_hsa_circ_243193,RMVar_hsa_circ_339161,RMVar_hsa_circ_243197 105953 RMVar_ID_105953 Human_SNP_ID_306793540 m1A Human chr7 - 712728 712728 712728 CGGCTGGAGTGGGCGACTCAGAGTCTGAGTGGAGGGGGCGGGGGGCGGCGACAGCGGGGGGTCCT CGGCTGGAGTGGGCGACTCAGAGTCTGAGTGGGGGGGGCGGGGGGCGGCGACAGCGGGGGGTCCT T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:712717..712880 26863196 MeRIP-seq:(Medium) rs1485221539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85211,RMVar_hsa_circ_243193 105954 RMVar_ID_105954 Human_SNP_ID_306793771 m1A Human chr7 + 713423 713423 713423 CGGCTTCCCTGTTGCCTACTCACCTGTCTCCCACTATGCTGCCCCATCTTCACCTGTCTCCCACT CGGCTTCCCTGTTGCCTACTCACCTGTCTCCCCCTATGCTGCCCCATCTTCACCTGTCTCCCACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:713419..713709 26863196 MeRIP-seq:(Medium) rs1030237433 Functional Loss SNV dbSNP153 33..33 33 - - - 105955 RMVar_ID_105955 Human_SNP_ID_306797909 m1A Human chr7 + 727136 727136 727136 CGTGCCCGCGCGCCGCCCGCCCGAGGCCTGTGAGGAGCTGCGCCTGGCGCTTGTGCAGCTGCTGG CGTGCCCGCGCGCCGCCCGCCCGAGGCCTGTGGGGAGCTGCGCCTGGCGCTTGTGCAGCTGCTGG A G DNAAF5 Ensembl:ENSG00000164818 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:726963..727246 26863196 MeRIP-seq:(Medium) rs1240120554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8914822,Human_RBP_ID_9311096,Human_RBP_ID_18195863,Human_RBP_ID_18885876,Human_RBP_ID_23080234 105956 RMVar_ID_105956 Human_SNP_ID_306810232 m1A Human chr7 + 763918 763918 763918 CCTCCTGGAGCGGGTGACCGCGTCGCACCTTGACTGGACCGCACACTCGCCGGAGCTCCTGCAGT CCTCCTGGAGCGGGTGACCGCGTCGCACCTTGTCTGGACCGCACACTCGCCGGAGCTCCTGCAGT A T DNAAF5 Ensembl:ENSG00000164818 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:756965..763932 32194978 MeRIP-seq:(Medium) rs1389749172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8914826,Human_RBP_ID_9311102,Human_RBP_ID_16229502,Human_RBP_ID_18196210 Human_Splice_Rec_836345,Human_Splice_Rec_836385,Human_Splice_Rec_836395 RMVar_hsa_circ_33905,RMVar_hsa_circ_124696,RMVar_hsa_circ_346582,RMVar_hsa_circ_90913,RMVar_hsa_circ_78013,RMVar_hsa_circ_120275,RMVar_hsa_circ_243200,RMVar_hsa_circ_243201,RMVar_hsa_circ_294072,RMVar_hsa_circ_243202,RMVar_hsa_circ_290239,RMVar_hsa_circ_243204,RMVar_hsa_circ_243205,RMVar_hsa_circ_243206,RMVar_hsa_circ_243207,RMVar_hsa_circ_14797,RMVar_hsa_circ_80705,RMVar_hsa_circ_126133,RMVar_hsa_circ_243208,RMVar_hsa_circ_29203 105957 RMVar_ID_105957 Human_SNP_ID_306811801 m1A Human chr7 - 768098 768098 768098 CACTTCCGCCCAGATCACCTGTCTCCGCTCCCAGCGCGAGCTCCCGCTCGCTGCACGGACACTTC CACTTCCGCCCAGATCACCTGTCTCCGCTCCCGGCGCGAGCTCCCGCTCGCTGCACGGACACTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:768096..768414 26863196 MeRIP-seq:(Medium) rs796139870 Functional Loss SNV dbSNP153 33..33 33 - - - 105958 RMVar_ID_105958 Human_SNP_ID_306811802 m1A Human chr7 - 768098 768098 768098 CACTTCCGCCCAGATCACCTGTCTCCGCTCCCAGCGCGAGCTCCCGCTCGCTGCACGGACACTTC CACTTCCGCCCAGATCACCTGTCTCCGCTCCCCGCGCGAGCTCCCGCTCGCTGCACGGACACTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:768096..768414 26863196 MeRIP-seq:(Medium) rs796139870 Functional Loss SNV dbSNP153 33..33 33 - - - 105959 RMVar_ID_105959 Human_SNP_ID_306824368 m1A Human chr7 + 802995 802991 802995 AAGGAAGGAAGGAAGGGAGACACAGAAAGAGAAAGAAGGAAAGAGAAAGAAAGAAAGAGAAAGAG AAGGAAGGAAGGAAGGGAGACACAGAAAG____AGAAGGAAAGAGAAAGAAAGAAAGAGAAAGAG GAGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:802960..803118 26863196 MeRIP-seq:(Medium) rs1337396284 Functional Loss DEL dbSNP153 30..33 33 - - - 105960 RMVar_ID_105960 Human_SNP_ID_306829368 m1A Human chr7 + 816672 816672 816672 CGCAGACGAGGCCTGAGGCGGCGGCGCGAGGCAGGTGAGCTCCCGGCGGGCCGGGCCAAGGGCAC CGCAGACGAGGCCTGAGGCGGCGGCGCGAGGCGGGTGAGCTCCCGGCGGGCCGGGCCAAGGGCAC A G SUN1 Ensembl:ENSG00000164828 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:816655..816736;chr7:816660..817106 26863196 MeRIP-seq:(Medium) rs1316627205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19135695 Human_Splice_Rec_836411,Human_Splice_Rec_836417,Human_Splice_Rec_836425,Human_Splice_Rec_836437,Human_Splice_Rec_836471,Human_Splice_Rec_836503,Human_Splice_Rec_836515 105961 RMVar_ID_105961 Human_SNP_ID_306829455 m1A Human chr7 - 816812 816812 816812 GCGGGACGGGCGGGGGCGGCAGCCGTTGGCCCAGGAGGCCCTGGCGCAGCCCGCGCTGAGGGCGC GCGGGACGGGCGGGGGCGGCAGCCGTTGGCCCGGGAGGCCCTGGCGCAGCCCGCGCTGAGGGCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:816809..817029 26863196 MeRIP-seq:(Medium) rs1308288063 Functional Loss SNV dbSNP153 33..33 33 - - - 105962 RMVar_ID_105962 Human_SNP_ID_306829640 m1A Human chr7 + 817199 817199 817199 CCAGGCTGGTCTCGACCTCCTGAGCGCGAGCTATCCTCCCGCCTCCGCCTCCCGAAGCGCTCGGA CCAGGCTGGTCTCGACCTCCTGAGCGCGAGCTGTCCTCCCGCCTCCGCCTCCCGAAGCGCTCGGA A G SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:817197..817294 26863196 MeRIP-seq:(Medium) rs28650941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1399648,Human_RBP_ID_18465903 105963 RMVar_ID_105963 Human_SNP_ID_306831599 m1A Human chr7 + 823407 823406 823408 GAACATTAAGTGTGAGGAGAAGTTAGCTAGGCAGAGTTTGGGGTGTAACTAGACCAAGGAGATGC GAACATTAAGTGTGAGGAGAAGTTAGCTAGGC__AGTTTGGGGTGTAACTAGACCAAGGAGATGC CAG C SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:823404..823533 26863196 MeRIP-seq:(Medium) rs1203615791 Functional Loss DEL dbSNP153 33..34 33 - - - 105964 RMVar_ID_105964 Human_SNP_ID_306834776 m1A Human chr7 - 832536 832536 832536 ACACACTGGGGAGGACTGTACATGTGAAGCCGAGAAAAATCCATGTTCACCACTTCAAACCATAC ACACACTGGGGAGGACTGTACATGTGAAGCCGGGAAAAATCCATGTTCACCACTTCAAACCATAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:832533..832638 26863196 MeRIP-seq:(Medium) rs965471886 Functional Loss SNV dbSNP153 33..33 33 - - - 105965 RMVar_ID_105965 Human_SNP_ID_306835283 m1A Human chr7 - 834117 834117 834117 AGTCTAAATTCCCAGCCCAGCCTACACCATCCAGCCAGCCCCTGCCCACCAAGAGTCTAAATTCC AGTCTAAATTCCCAGCCCAGCCTACACCATCCGGCCAGCCCCTGCCCACCAAGAGTCTAAATTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:834004..834375 26863196 MeRIP-seq:(Medium) rs13221885 Functional Loss SNV dbSNP153 33..33 33 - - - 105966 RMVar_ID_105966 Human_SNP_ID_306837926 m1A Human chr7 - 841999 841999 841999 GGCTGACGCCAGAGGACGTGACCTGCCTTGACACGTGGTTGATACTAAAAGCTGATTTGTTTGTG GGCTGACGCCAGAGGACGTGACCTGCCTTGACGCGTGGTTGATACTAAAAGCTGATTTGTTTGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:841926..842150 26863196 MeRIP-seq:(Medium) rs772702463 Functional Loss SNV dbSNP153 33..33 33 - - - 105967 RMVar_ID_105967 Human_SNP_ID_306838389 m1A Human chr7 - 843354 843354 843354 GCGGCTCCCACATCCCCGTTTCCCTGAATGGCAGCTTTATTTCCACCTAAAGTTTTCAAACAGTA GCGGCTCCCACATCCCCGTTTCCCTGAATGGCGGCTTTATTTCCACCTAAAGTTTTCAAACAGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:843343..843472 26863196 MeRIP-seq:(Medium) rs1227863699 Functional Loss SNV dbSNP153 33..33 33 - - - 105968 RMVar_ID_105968 Human_SNP_ID_306840761 m1A Human chr7 - 849882 849882 849882 GTGGTGACAGGCAGTGAGTGTGGCGGATTCACAAGCAAACTCTGTCCATCTCAGCCGTGCATAGC GTGGTGACAGGCAGTGAGTGTGGCGGATTCACTAGCAAACTCTGTCCATCTCAGCCGTGCATAGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:849881..849967 26863196 MeRIP-seq:(Medium) rs771316032 Functional Loss SNV dbSNP153 33..33 33 - - - 105969 RMVar_ID_105969 Human_SNP_ID_306840762 m1A Human chr7 - 849882 849882 849882 GTGGTGACAGGCAGTGAGTGTGGCGGATTCACAAGCAAACTCTGTCCATCTCAGCCGTGCATAGC GTGGTGACAGGCAGTGAGTGTGGCGGATTCACCAGCAAACTCTGTCCATCTCAGCCGTGCATAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:849881..849967 26863196 MeRIP-seq:(Medium) rs771316032 Functional Loss SNV dbSNP153 33..33 33 - - - 105970 RMVar_ID_105970 Human_SNP_ID_306847262 m1A Human chr7 - 868626 868626 868626 AGCACTGTCCCCCCATCCGACCAACACCACAGAGAACCAGCACTGCCCCCCCATCCGACCAACAC AGCACTGTCCCCCCATCCGACCAACACCACAGGGAACCAGCACTGCCCCCCCATCCGACCAACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:868397..868684;chr7:868550..868683 26863196 MeRIP-seq:(Medium) rs1207988303 Functional Loss SNV dbSNP153 33..33 33 - - - 105971 RMVar_ID_105971 Human_SNP_ID_306850337 m1A Human chr7 + 876622 876622 876622 GAGGCGCTGCCGACCGCGCCTGCGACAGCGTCAGCCCTGCGCGGAGCGCCGGCCCGATGGCGGCG GAGGCGCTGCCGACCGCGCCTGCGACAGCGTCGGCCCTGCGCGGAGCGCCGGCCCGATGGCGGCG A G GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:876576..876726;chr7:876576..876729 26863196 MeRIP-seq:(Medium) rs1344455774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955555,Human_RBP_ID_9336874,Human_RBP_ID_18425946,Human_RBP_ID_18886863,Human_RBP_ID_22110534 RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239 105972 RMVar_ID_105972 Human_SNP_ID_306851024 m1A Human chr7 - 877711 877711 877711 AGGGGCGGTGGAGCCGGAGAACAGGGAGGGGGAGGCCGGGCAGGGAGATCTGGGACAGGGAGATA AGGGGCGGTGGAGCCGGAGAACAGGGAGGGGGGGGCCGGGCAGGGAGATCTGGGACAGGGAGATA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:877668..877838 26863196 MeRIP-seq:(Medium) rs1321378020 Functional Loss SNV dbSNP153 33..33 33 - - - 105973 RMVar_ID_105973 Human_SNP_ID_306855882 m1A Human chr7 + 889698 889677 889698 TAGGACGGGGTCTGGGGCGAGCGGGTGTTAGGACGGGCCTGGGAGCGGAGGGAGTGCGAGCGGGT TAGGACGGGGTC_____________________CGGGCCTGGGAGCGGAGGGAGTGCGAGCGGGT CTGGGGCGAGCGGGTGTTAGGA C GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:889505..889770;chr7:889620..889766 26863196 MeRIP-seq:(Medium) rs1181894928 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_8217361,Human_RBP_ID_21992167 RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239,RMVar_hsa_circ_373973,RMVar_hsa_circ_243243 105974 RMVar_ID_105974 Human_SNP_ID_306855897 m1A Human chr7 + 889698 889693 889698 TAGGACGGGGTCTGGGGCGAGCGGGTGTTAGGACGGGCCTGGGAGCGGAGGGAGTGCGAGCGGGT TAGGACGGGGTCTGGGGCGAGCGGGTGT_____CGGGCCTGGGAGCGGAGGGAGTGCGAGCGGGT TTAGGA T GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:889505..889770;chr7:889620..889766 26863196 MeRIP-seq:(Medium) rs1359467762 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_8217361,Human_RBP_ID_21992167 RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239,RMVar_hsa_circ_373973,RMVar_hsa_circ_243243 105975 RMVar_ID_105975 Human_SNP_ID_306856175 m1A Human chr7 - 890409 890330 890410 CTCACACTCCCTCCACTCCCAGGCCCGTCCTAACACCCGCTCACACTCCCTCCACTCCCAGACCC CTCACACTCCCTCCACTCCCAGGCCCGTCCT__________________________________ CAGGACGGGGTCTGGGAGTGGAGGGAGTGCGAGCGGGTGTCAGGACGGGGTCTGGGAGTGGAGGGAGTGTGAGCGGGTGTT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:890407..890509 26863196 MeRIP-seq:(Medium) rs1562896572 Functional Loss DEL dbSNP153 32..65 33 - - - 105976 RMVar_ID_105976 Human_SNP_ID_306857859 m1A Human chr7 - 893354 893354 893354 ACCTGCACACACCACGCCCACACCCAACACTCACCTGCAACCACCACCACGCCCGCGCCCAACAC ACCTGCACACACCACGCCCACACCCAACACTCCCCTGCAACCACCACCACGCCCGCGCCCAACAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:892417..893704 26863196 MeRIP-seq:(Medium) rs1315077111 Functional Loss SNV dbSNP153 33..33 33 - - - 105977 RMVar_ID_105977 Human_SNP_ID_306857918 m1A Human chr7 - 893427 893426 893428 CCAACACTCACCTGCAACCATGCCTGCACCCAACACTCACCTGCACACACCACCGCGCCCACGCC CCAACACTCACCTGCAACCATGCCTGCACCC__CACTCACCTGCACACACCACCGCGCCCACGCC GTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:892426..893700 26863196 MeRIP-seq:(Medium) rs1184888187 Functional Loss DEL dbSNP153 32..33 33 - - - 105978 RMVar_ID_105978 Human_SNP_ID_306857920 m1A Human chr7 - 893427 893427 893427 CCAACACTCACCTGCAACCATGCCTGCACCCAACACTCACCTGCACACACCACCGCGCCCACGCC CCAACACTCACCTGCAACCATGCCTGCACCCAGCACTCACCTGCACACACCACCGCGCCCACGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:892426..893700 26863196 MeRIP-seq:(Medium) rs1461429171 Functional Loss SNV dbSNP153 33..33 33 - - - 105979 RMVar_ID_105979 Human_SNP_ID_306857932 m1A Human chr7 - 893450 893450 893450 TGCACAAACCACCGCGCCCGCGCCCAACACTCACCTGCAACCATGCCTGCACCCAACACTCACCT TGCACAAACCACCGCGCCCGCGCCCAACACTCGCCTGCAACCATGCCTGCACCCAACACTCACCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:892829..893605 26863196 MeRIP-seq:(Medium) rs1476422221 Functional Loss SNV dbSNP153 33..33 33 - - - 105980 RMVar_ID_105980 Human_SNP_ID_306859399 m1A Human chr7 - 895573 895573 895573 GCAGCACAGTGAGCAGCAGCCGCGCCACCCTGAGCCGCCGCACAGAAACAGACACGCGCCGGCAT GCAGCACAGTGAGCAGCAGCCGCGCCACCCTGCGCCGCCGCACAGAAACAGACACGCGCCGGCAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:895524..895602 26863196 MeRIP-seq:(Medium) rs1377111309 Functional Loss SNV dbSNP153 33..33 33 - - - 105981 RMVar_ID_105981 Human_SNP_ID_306859411 m1A Human chr7 - 895588 895588 895588 CACTCTTGGGTCCCAGCAGCACAGTGAGCAGCAGCCGCGCCACCCTGAGCCGCCGCACAGAAACA CACTCTTGGGTCCCAGCAGCACAGTGAGCAGCTGCCGCGCCACCCTGAGCCGCCGCACAGAAACA T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:895487..895637 26863410 MeRIP-seq:(Medium) rs1017693276 Functional Loss SNV dbSNP153 33..33 33 - - - 105982 RMVar_ID_105982 Human_SNP_ID_306861284 m1A Human chr7 - 898791 898788 898791 CCACCTGCTCCTCAGGGCAGCCCGGCGCGGCCAGGTAGGGCCCGAGCTTCAGCTTCCAGGATGCT CCACCTGCTCCTCAGGGCAGCCCGGCGCGGCC___TAGGGCCCGAGCTTCAGCTTCCAGGATGCT ACCT A ADAP1,COX19 Ensembl:ENSG00000105963,Ensembl:ENSG00000240230 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:898743..899076 32194978 MeRIP-seq:(Medium) rs1446345629 Functional Loss DEL dbSNP153 33..35 33 - - - 105983 RMVar_ID_105983 Human_SNP_ID_306861495 m1A Human chr7 + 899117 899117 899117 CACCCACTCCCTCTGGTCGGACTCCGTCTCGCAGGCAAACAGAAACTTGCGGTCGGGCGTGACGA CACCCACTCCCTCTGGTCGGACTCCGTCTCGCCGGCAAACAGAAACTTGCGGTCGGGCGTGACGA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:898942..899175 26863410 MeRIP-seq:(Medium) rs1342609947 Functional Loss SNV dbSNP153 33..33 33 - - - 105984 RMVar_ID_105984 Human_SNP_ID_306862045 m1A Human chr7 - 900129 900129 900129 GTGCCAAAGCTCTCCAGGAACTACCTGAAGGAAGGCTACATGGAGAAGACGGGGCCCAAGGTGGG GTGCCAAAGCTCTCCAGGAACTACCTGAAGGAGGGCTACATGGAGAAGACGGGGCCCAAGGTGGG T C ADAP1,COX19 Ensembl:ENSG00000105963,Ensembl:ENSG00000240230 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:900127..966087 32194978 MeRIP-seq:(Medium) rs1208591061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_836968,Human_Splice_Rec_836969,Human_Splice_Rec_836984,Human_Splice_Rec_836985,Human_Splice_Rec_837002,Human_Splice_Rec_837003,Human_Splice_Rec_837022,Human_Splice_Rec_837023,Human_Splice_Rec_837042,Human_Splice_Rec_837043,Human_Splice_Rec_837062,Human_Splice_Rec_837063,Human_Splice_Rec_837080,Human_Splice_Rec_837081,Human_Splice_Rec_837092,Human_Splice_Rec_837093,Human_Splice_Rec_837100,Human_Splice_Rec_837101,Human_Splice_Rec_837114,Human_Splice_Rec_837115,Human_Splice_Rec_837130,Human_Splice_Rec_837131,Human_Splice_Rec_837144,Human_Splice_Rec_837210,Human_Splice_Rec_837211 RMVar_hsa_circ_243245,RMVar_hsa_circ_377670 105985 RMVar_ID_105985 Human_SNP_ID_306862310 m1A Human chr7 - 900587 900587 900587 TAGGAGATTGTGGACTGGTTCAATGCACTCCGAGCTGCTCGCTTCCACTACCTGCAGGTGGCATT TAGGAGATTGTGGACTGGTTCAATGCACTCCGGGCTGCTCGCTTCCACTACCTGCAGGTGGCATT T C ADAP1,COX19 Ensembl:ENSG00000105963,Ensembl:ENSG00000240230 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:900558..900658 26863196 MeRIP-seq:(Medium) rs1294625243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_836966,Human_Splice_Rec_836967,Human_Splice_Rec_836982,Human_Splice_Rec_836983,Human_Splice_Rec_837000,Human_Splice_Rec_837001,Human_Splice_Rec_837020,Human_Splice_Rec_837021,Human_Splice_Rec_837040,Human_Splice_Rec_837041,Human_Splice_Rec_837060,Human_Splice_Rec_837061,Human_Splice_Rec_837078,Human_Splice_Rec_837079,Human_Splice_Rec_837090,Human_Splice_Rec_837091,Human_Splice_Rec_837099,Human_Splice_Rec_837112,Human_Splice_Rec_837113,Human_Splice_Rec_837128,Human_Splice_Rec_837129,Human_Splice_Rec_837142,Human_Splice_Rec_837143,Human_Splice_Rec_837154,Human_Splice_Rec_837208,Human_Splice_Rec_837209 RMVar_hsa_circ_243245,RMVar_hsa_circ_377670 105986 RMVar_ID_105986 Human_SNP_ID_306865946 m1A Human chr7 + 905650 905650 905650 AAAGGGAAAGGAGAAAGGGAAAGGAGAAAGGGAAAGGAGAAAGGAGAAAGGAGAAAGGGAAAGGA AAAGGGAAAGGAGAAAGGGAAAGGAGAAAGGGGAAGGAGAAAGGAGAAAGGAGAAAGGGAAAGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:905592..905716 26863196 MeRIP-seq:(Medium) rs1284258125 Functional Loss SNV dbSNP153 33..33 33 - - - 105987 RMVar_ID_105987 Human_SNP_ID_306866407 m1A Human chr7 + 906024 906024 906024 AAAGGAGAAAGGAGAAAGGAGAAAGGGAAAGGAGAAAGGAGAAAGGGAAAGGAGAAAGGAGAAAG AAAGGAGAAAGGAGAAAGGAGAAAGGGAAAGGGGAAAGGAGAAAGGGAAAGGAGAAAGGAGAAAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:906004..906087 26863196 MeRIP-seq:(Medium) rs868561801 Functional Loss SNV dbSNP153 33..33 33 - - - 105988 RMVar_ID_105988 Human_SNP_ID_306890031 m1A Human chr7 + 967879 967879 967879 ACTGCGTTGGCGAGCTCATGGCACGTGGCCACACCGCGTCAGCGCCGACTCCACGGTGGCTGCGT ACTGCGTTGGCGAGCTCATGGCACGTGGCCACGCCGCGTCAGCGCCGACTCCACGGTGGCTGCGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:967833..967934 32194978 MeRIP-seq:(Medium) rs990760444 Functional Loss SNV dbSNP153 33..33 33 - - - 105989 RMVar_ID_105989 Human_SNP_ID_306892308 m1A Human chr7 - 975485 975485 975485 TCGCCAACATGTCGACCGCCATGAATTTCGGGACCAAGAGCTTCCAGCCGCGGCCCCCGGACAAG TCGCCAACATGTCGACCGCCATGAATTTCGGGTCCAAGAGCTTCCAGCCGCGGCCCCCGGACAAG T A COX19 Ensembl:ENSG00000240230 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:975374..975515 26863196 MeRIP-seq:(Medium) rs770842621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954044,Human_RBP_ID_15948709,Human_RBP_ID_18426144,Human_RBP_ID_18872766,Human_RBP_ID_23080021 Human_Splice_Rec_837195,Human_Splice_Rec_837217,Human_Splice_Rec_837221 105990 RMVar_ID_105990 Human_SNP_ID_306895951 m1A Human chr7 + 986576 986576 986576 CGCTGGGGACGATCACCGCCTGCCCAGCGTGCAGCCCTGGGGCTGCGTCCTTATCTCCGCTCCTC CGCTGGGGACGATCACCGCCTGCCCAGCGTGCGGCCCTGGGGCTGCGTCCTTATCTCCGCTCCTC A G CYP2W1 Ensembl:ENSG00000073067 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:986548..986657 26863196 MeRIP-seq:(Medium) rs767378036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22554502,Human_RBP_ID_22686248 105991 RMVar_ID_105991 Human_SNP_ID_306896971 m1A Human chr7 - 988680 988680 988680 GGTACCTCTGCAGGAGGCCGGCAAACAGCAGGAAGAGCTCGGTCCTGGCCAGGCGCTCCCCAACA GGTACCTCTGCAGGAGGCCGGCAAACAGCAGGTAGAGCTCGGTCCTGGCCAGGCGCTCCCCAACA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:988670..988845 26863196 MeRIP-seq:(Medium) rs746607365 Functional Loss SNV dbSNP153 33..33 33 - - - 105992 RMVar_ID_105992 Human_SNP_ID_306899865 m1A Human chr7 + 997140 997140 997140 CGCAATGACGCTGTGTGGGGTCAAAGGAAAACAGGCCACAGCCAGGCCCCTCGATGGACGCAGGC CGCAATGACGCTGTGTGGGGTCAAAGGAAAACTGGCCACAGCCAGGCCCCTCGATGGACGCAGGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:997092..997249 26863196 MeRIP-seq:(Medium) rs1204470980 Functional Loss SNV dbSNP153 33..33 33 - - - 105993 RMVar_ID_105993 Human_SNP_ID_306900096 m1A Human chr7 - 997695 997695 997695 GAAGGCGGAAGCCCTGATGCGGGAGCTGGATGAGGAGGGCTCTGATCCCCCCCTGCCGGGGAGGG GAAGGCGGAAGCCCTGATGCGGGAGCTGGATGGGGAGGGCTCTGATCCCCCCCTGCCGGGGAGGG T C C7orf50 Ensembl:ENSG00000146540 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:997645..997735 26863196 MeRIP-seq:(Medium) rs147627148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_672112,Human_RBP_ID_3971715,Human_RBP_ID_17665201,Human_RBP_ID_19019360 RMVar_hsa_circ_1847 105994 RMVar_ID_105994 Human_SNP_ID_306901198 m1A Human chr7 + 1000550 1000550 1000550 CTGAAACCTCCAGTTCTTGTGCTTTTGGGCCCATCTAGGGAAAGAAAGACAAACATCTCAGGGTG CTGAAACCTCCAGTTCTTGTGCTTTTGGGCCCGTCTAGGGAAAGAAAGACAAACATCTCAGGGTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1000451..1000575 32194978 MeRIP-seq:(Medium) rs765752020 Functional Loss SNV dbSNP153 33..33 33 - - - 105995 RMVar_ID_105995 Human_SNP_ID_306912619 m1A Human chr7 - 1028193 1028193 1028193 CTGCAGGGAGGGGATGGGAGGGGCCCTGCCCCAGCCCCGCCCCGCGGCGACAGGTGGGCGCTCCC CTGCAGGGAGGGGATGGGAGGGGCCCTGCCCCGGCCCCGCCCCGCGGCGACAGGTGGGCGCTCCC T C C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1028179..1028301 26863196 MeRIP-seq:(Medium) rs1386133620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3861457,Human_RBP_ID_5134715,Human_RBP_ID_5220445,Human_RBP_ID_5327681,Human_RBP_ID_5401345,Human_RBP_ID_8149866,Human_RBP_ID_8217462,Human_RBP_ID_18503398,Human_RBP_ID_22729000,Human_RBP_ID_26793468 105996 RMVar_ID_105996 Human_SNP_ID_306912856 m1A Human chr7 - 1028710 1028680 1028710 TGGGTCTATGGGGGCAGATTGGGGGAGATGAGAGGATAATGGAGGCAGATGGGGGAGATGAGGGA TGGGTCTATGGGGGCAGATTGGGGGAGATGAG______________________________GGA CCTCATCTCCCCCATCTGCCTCCATTATCCT C C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1028706..1028911 26863196 MeRIP-seq:(Medium) rs1195064803 Functional Loss DEL dbSNP153 33..62 33 - - - 105997 RMVar_ID_105997 Human_SNP_ID_306915179 m1A Human chr7 - 1036320 1036320 1036320 GAGCCCTGCACGGCCACAGCACGAGCACCCGAACCCTGCACGGCCACAGCACGAGCACCCGAACC GAGCCCTGCACGGCCACAGCACGAGCACCCGAGCCCTGCACGGCCACAGCACGAGCACCCGAACC T C C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1036317..1036408 26863196 MeRIP-seq:(Medium) rs559063882 Functional Loss SNV dbSNP153 33..33 33 - - - 105998 RMVar_ID_105998 Human_SNP_ID_306915233 m1A Human chr7 - 1036403 1036403 1036403 ACACGGCCACACCACGAGCACCCGAGCCCTGCACGGCCACAGCACGAGCACCCGAGCCCTGCACG ACACGGCCACACCACGAGCACCCGAGCCCTGCCCGGCCACAGCACGAGCACCCGAGCCCTGCACG T G C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1036400..1036541 26863196 MeRIP-seq:(Medium) rs1451829964 Functional Loss SNV dbSNP153 33..33 33 - - - 105999 RMVar_ID_105999 Human_SNP_ID_306921854 m1A Human chr7 - 1056384 1056384 1056384 TCATTGTGCAATCCTGGTGAATGCCGCCCAGCAGCCGCAGTGAGGGTCAGGTGGTGACAGGCATG TCATTGTGCAATCCTGGTGAATGCCGCCCAGCGGCCGCAGTGAGGGTCAGGTGGTGACAGGCATG T C AC073957.2,C7orf50 Ensembl:ENSG00000257607,Ensembl:ENSG00000146540 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1056378..1056566 26863196 MeRIP-seq:(Medium) rs903226200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3861469,Human_RBP_ID_5105201,Human_RBP_ID_5656828,Human_RBP_ID_8149008,Human_RBP_ID_8238226,Human_RBP_ID_9439535,Human_RBP_ID_22728502,Human_RBP_ID_24389270 106000 RMVar_ID_106000 Human_SNP_ID_306928357 m1A Human chr7 - 1073358 1073358 1073358 GGAGCTGCCTGCGCGGGGAGTAGCTGCCGGCCACTTGTCTCCGAAACGGGAGTGGAATGCGGTGA GGAGCTGCCTGCGCGGGGAGTAGCTGCCGGCCCCTTGTCTCCGAAACGGGAGTGGAATGCGGTGA T G C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1073355..1073736 26863196 MeRIP-seq:(Medium) rs978195532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3861521,Human_RBP_ID_5153538,Human_RBP_ID_5657378,Human_RBP_ID_8149017,Human_RBP_ID_8217537,Human_RBP_ID_8238227,Human_RBP_ID_8730603,Human_RBP_ID_9439537,Human_RBP_ID_17170025,Human_RBP_ID_22703954,Human_RBP_ID_22728513 106001 RMVar_ID_106001 Human_SNP_ID_306928611 m1A Human chr7 + 1073938 1073938 1073938 CCCGACCCCGCACCCCGCCGCCGTCACGCCCGACCCCTCACCCCGCTACTGTGACGCCCCCCGAC CCCGACCCCGCACCCCGCCGCCGTCACGCCCGCCCCCTCACCCCGCTACTGTGACGCCCCCCGAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1073932..1074009 26863196 MeRIP-seq:(Medium) rs1181721046 Functional Loss SNV dbSNP153 33..33 33 - - - 106002 RMVar_ID_106002 Human_SNP_ID_306928612 m1A Human chr7 + 1073938 1073938 1073938 CCCGACCCCGCACCCCGCCGCCGTCACGCCCGACCCCTCACCCCGCTACTGTGACGCCCCCCGAC CCCGACCCCGCACCCCGCCGCCGTCACGCCCGTCCCCTCACCCCGCTACTGTGACGCCCCCCGAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1073932..1074009 26863196 MeRIP-seq:(Medium) rs1181721046 Functional Loss SNV dbSNP153 33..33 33 - - - 106003 RMVar_ID_106003 Human_SNP_ID_306946138 m1A Human chr7 - 1127356 1127356 1127356 AGGATGGCAAAACAGAAGAGAAAAGTTCCTGAAGTGACAGAGAAAAAGAACAAAAAGCTGAAGAA AGGATGGCAAAACAGAAGAGAAAAGTTCCTGACGTGACAGAGAAAAAGAACAAAAAGCTGAAGAA T G C7orf50 Ensembl:ENSG00000146540 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1127208..1127427 26863196 MeRIP-seq:(Medium) rs1215576469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837270,Human_Splice_Rec_837271,Human_Splice_Rec_837278,Human_Splice_Rec_837279,Human_Splice_Rec_837286,Human_Splice_Rec_837287,Human_Splice_Rec_837299,Human_Splice_Rec_837314,Human_Splice_Rec_837315 RMVar_hsa_circ_365515 106004 RMVar_ID_106004 Human_SNP_ID_306950441 m1A Human chr7 - 1138237 1138237 1138237 GCGCGGGTCCCTGCCGGAAGGCGGCGTCCGCGACGCAGCTGTTCACGCTTAGGTGGGCGACGTGG GCGCGGGTCCCTGCCGGAAGGCGGCGTCCGCGGCGCAGCTGTTCACGCTTAGGTGGGCGACGTGG T C C7orf50 Ensembl:ENSG00000146540 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:1138131..1138275;chr7:1138116..1138275 26863196 MeRIP-seq:(Medium) rs944215298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4957605 Human_Splice_Rec_837269,Human_Splice_Rec_837277,Human_Splice_Rec_837313 106005 RMVar_ID_106005 Human_SNP_ID_306955022 m1A Human chr7 + 1153210 1153210 1153210 ATCTCTTTCTTCTTGCAGCCCTCTTTTGAGCAACGGTATGTAAAAATCTAAGAGAGCAAAGTGAC ATCTCTTTCTTCTTGCAGCCCTCTTTTGAGCATCGGTATGTAAAAATCTAAGAGAGCAAAGTGAC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1153173..1157025 32194978 MeRIP-seq:(Medium) rs758955588 Functional Loss SNV dbSNP153 33..33 33 - - - 106006 RMVar_ID_106006 Human_SNP_ID_306956939 m1A Human chr7 - 1158190 1158190 1158190 TGTTCTCATAATGGAGTTTCCTGATTTGGGGAAGCATTGTTCAGAAAAGACTTGCAAGCAGCTAG TGTTCTCATAATGGAGTTTCCTGATTTGGGGAGGCATTGTTCAGAAAAGACTTGCAAGCAGCTAG T C ZFAND2A Ensembl:ENSG00000178381 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1157712..1158218 32194978 MeRIP-seq:(Medium) rs762274671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953017,Human_RBP_ID_2034068,Human_RBP_ID_5122659,Human_RBP_ID_9203491,Human_RBP_ID_17665203,Human_RBP_ID_18874834,Human_RBP_ID_19019362,Human_RBP_ID_22619621,Human_RBP_ID_22833113,Human_RBP_ID_24186616 Human_Splice_Rec_837358,Human_Splice_Rec_837359,Human_Splice_Rec_837374,Human_Splice_Rec_837375,Human_Splice_Rec_837382,Human_Splice_Rec_837383,Human_Splice_Rec_837390,Human_Splice_Rec_837391 RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 106007 RMVar_ID_106007 Human_SNP_ID_306956940 m1A Human chr7 - 1158190 1158190 1158190 TGTTCTCATAATGGAGTTTCCTGATTTGGGGAAGCATTGTTCAGAAAAGACTTGCAAGCAGCTAG TGTTCTCATAATGGAGTTTCCTGATTTGGGGACGCATTGTTCAGAAAAGACTTGCAAGCAGCTAG T G ZFAND2A Ensembl:ENSG00000178381 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1157712..1158218 32194978 MeRIP-seq:(Medium) rs762274671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953017,Human_RBP_ID_2034068,Human_RBP_ID_5122659,Human_RBP_ID_9203491,Human_RBP_ID_17665203,Human_RBP_ID_18874834,Human_RBP_ID_19019362,Human_RBP_ID_22619621,Human_RBP_ID_22833113,Human_RBP_ID_24186616 Human_Splice_Rec_837358,Human_Splice_Rec_837359,Human_Splice_Rec_837374,Human_Splice_Rec_837375,Human_Splice_Rec_837382,Human_Splice_Rec_837383,Human_Splice_Rec_837390,Human_Splice_Rec_837391 RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 106008 RMVar_ID_106008 Human_SNP_ID_306958027 m1A Human chr7 - 1160472 1160472 1160472 CTCGCGCTCCTACCCCGCAGGACCCCGGCCGCAGCCCTGAGTCAGCTTCCCCGCTCCTCGCCCGC CTCGCGCTCCTACCCCGCAGGACCCCGGCCGCGGCCCTGAGTCAGCTTCCCCGCTCCTCGCCCGC T C ZFAND2A Ensembl:ENSG00000178381 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1160422..1162395 26863196 MeRIP-seq:(Medium) rs922041430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5403581 Human_Splice_Rec_837394 106009 RMVar_ID_106009 Human_SNP_ID_307049842 m1A Human chr7 - 1435128 1435128 1435128 GGTCCCGTTTCAGGGAACAAGAGGAGGATCAGATGCTGCGGGACATGATTGAGAAGCTGGGTGAC GGTCCCGTTTCAGGGAACAAGAGGAGGATCAGGTGCTGCGGGACATGATTGAGAAGCTGGGTGAC T C MICALL2 Ensembl:ENSG00000164877 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1435040..1435291 26863196 MeRIP-seq:(Medium) rs762878613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970679,Human_RBP_ID_16055314,Human_RBP_ID_17664340,Human_RBP_ID_18171627,Human_RBP_ID_19020411,Human_RBP_ID_24197978,Human_RBP_ID_26356124,Human_RBP_ID_27830128 Human_Splice_Rec_837466,Human_Splice_Rec_837500,Human_Splice_Rec_837501,Human_Splice_Rec_837518,Human_Splice_Rec_837519,Human_Splice_Rec_837526,Human_Splice_Rec_837527,Human_Splice_Rec_837552,Human_Splice_Rec_837553,Human_Splice_Rec_837582,Human_Splice_Rec_837583 RMVar_hsa_circ_91852,RMVar_hsa_circ_95469,RMVar_hsa_circ_243255,RMVar_hsa_circ_243256 106010 RMVar_ID_106010 Human_SNP_ID_307050587 m1A Human chr7 - 1436751 1436751 1436751 CCGCAGTGACATCGTGGACTCGCTGGACGAGGACCGGCTCCGGTGAGGGGCAGGTGCCGGGGGCC CCGCAGTGACATCGTGGACTCGCTGGACGAGGGCCGGCTCCGGTGAGGGGCAGGTGCCGGGGGCC T C MICALL2 Ensembl:ENSG00000164877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1436741..1436818 26863196 MeRIP-seq:(Medium) rs765136018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19020412,Human_RBP_ID_19135750 Human_Splice_Rec_837437,Human_Splice_Rec_837465,Human_Splice_Rec_837499,Human_Splice_Rec_837517,Human_Splice_Rec_837525,Human_Splice_Rec_837539,Human_Splice_Rec_837551,Human_Splice_Rec_837581 RMVar_hsa_circ_26932,RMVar_hsa_circ_91852,RMVar_hsa_circ_95469,RMVar_hsa_circ_243255,RMVar_hsa_circ_243256,RMVar_hsa_circ_86404,RMVar_hsa_circ_243257 106011 RMVar_ID_106011 Human_SNP_ID_307051086 m1A Human chr7 - 1437603 1437603 1437603 GGCCTCAGACGCGTGTCTGTGCGGCAGGTCCAAGGCCCAGCGTCTGGAGGAGCAGCAGCTGGACA GGCCTCAGACGCGTGTCTGTGCGGCAGGTCCAGGGCCCAGCGTCTGGAGGAGCAGCAGCTGGACA T C MICALL2 Ensembl:ENSG00000164877 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1437596..1437711 26863196 MeRIP-seq:(Medium) rs1157568894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970684,Human_RBP_ID_9404180,Human_RBP_ID_19020414,Human_RBP_ID_23080242,Human_RBP_ID_26356127,Human_RBP_ID_27830129 Human_Splice_Rec_837433,Human_Splice_Rec_837436,Human_Splice_Rec_837462,Human_Splice_Rec_837463,Human_Splice_Rec_837496,Human_Splice_Rec_837497,Human_Splice_Rec_837514,Human_Splice_Rec_837515,Human_Splice_Rec_837522,Human_Splice_Rec_837536,Human_Splice_Rec_837537,Human_Splice_Rec_837548,Human_Splice_Rec_837549,Human_Splice_Rec_837578,Human_Splice_Rec_837579,Human_Splice_Rec_837588,Human_Splice_Rec_837589,Human_Splice_Rec_837594 RMVar_hsa_circ_26932,RMVar_hsa_circ_91852,RMVar_hsa_circ_95469,RMVar_hsa_circ_243255,RMVar_hsa_circ_243256,RMVar_hsa_circ_243258,RMVar_hsa_circ_125876,RMVar_hsa_circ_58253 106012 RMVar_ID_106012 Human_SNP_ID_307052943 m1A Human chr7 + 1440550 1440550 1440550 GATTACATACTCACTGCATTTATTAAGCACCTATGGTGTACCAGGCCCTGGGCCAGCCCCACCCA GATTACATACTCACTGCATTTATTAAGCACCTGTGGTGTACCAGGCCCTGGGCCAGCCCCACCCA A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1440501..1440687 26863196 MeRIP-seq:(Medium) rs924829087 Functional Loss SNV dbSNP153 33..33 33 - - - 106013 RMVar_ID_106013 Human_SNP_ID_307053005 m1A Human chr7 - 1440641 1440641 1440641 AGCCTCCAGGAAGGCCAGGAGGACGGGCCGGCAGGATGGAGAGCGAATCTGAAGCCCGTGGACAG AGCCTCCAGGAAGGCCAGGAGGACGGGCCGGCGGGATGGAGAGCGAATCTGAAGCCCGTGGACAG T C MICALL2 Ensembl:ENSG00000164877 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:1440526..1440701;chr7:1440512..1440728;chr7:1440496..1440726 26863196 MeRIP-seq:(Medium) rs1333607215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19020422,Human_RBP_ID_22685097,Human_RBP_ID_24563193,Human_RBP_ID_26131299 Human_Splice_Rec_837451,Human_Splice_Rec_837484,Human_Splice_Rec_837485,Human_Splice_Rec_837503,Human_Splice_Rec_837566,Human_Splice_Rec_837567 RMVar_hsa_circ_91852,RMVar_hsa_circ_243256,RMVar_hsa_circ_58253,RMVar_hsa_circ_62289,RMVar_hsa_circ_354453,RMVar_hsa_circ_45589,RMVar_hsa_circ_77886,RMVar_hsa_circ_243260 106014 RMVar_ID_106014 Human_SNP_ID_307053878 m1A Human chr7 - 1442559 1442559 1442559 GGCTGGGCATTGGGAGTGAGCTGCAGGGAGGCAGAGGGGCGGCCTCGGGTGATGGTGGGAGGGCG GGCTGGGCATTGGGAGTGAGCTGCAGGGAGGCGGAGGGGCGGCCTCGGGTGATGGTGGGAGGGCG T C MICALL2 Ensembl:ENSG00000164877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1442550..1442622 26863196 MeRIP-seq:(Medium) rs964906928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267565,Human_RBP_ID_3860282,Human_RBP_ID_5327698,Human_RBP_ID_5401352,Human_RBP_ID_8149911,Human_RBP_ID_8237804,Human_RBP_ID_9337616,Human_RBP_ID_9439547,Human_RBP_ID_22619651,Human_RBP_ID_22685102 RMVar_hsa_circ_91852,RMVar_hsa_circ_243256,RMVar_hsa_circ_77886,RMVar_hsa_circ_243260 106015 RMVar_ID_106015 Human_SNP_ID_307054983 m1A Human chr7 - 1444872 1444872 1444872 CCACACTCAGTTCAAGCTCCACATCTGCAGCCACGGTGGACCCCCCAGCCTGGACCCCGTCCGCC CCACACTCAGTTCAAGCTCCACATCTGCAGCCGCGGTGGACCCCCCAGCCTGGACCCCGTCCGCC T C MICALL2 Ensembl:ENSG00000164877 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1444762..1445103 26863196 MeRIP-seq:(Medium) rs762061682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970706,Human_RBP_ID_5220781,Human_RBP_ID_17092802,Human_RBP_ID_26356136,Human_RBP_ID_27842800 Human_miRNA_ID_2027109,Human_miRNA_ID_2683804 RMVar_hsa_circ_91852,RMVar_hsa_circ_243256,RMVar_hsa_circ_77886,RMVar_hsa_circ_243260 106016 RMVar_ID_106016 Human_SNP_ID_307054993 m1A Human chr7 + 1444887 1444887 1444887 GGCTGGGGGGTCCACCGTGGCTGCAGATGTGGAGCTTGAACTGAGTGTGGTTTGAGGAGCTGCCA GGCTGGGGGGTCCACCGTGGCTGCAGATGTGGCGCTTGAACTGAGTGTGGTTTGAGGAGCTGCCA A C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1444855..1445020 26863196 MeRIP-seq:(Medium) rs752665765 Functional Loss SNV dbSNP153 33..33 33 - - - 106017 RMVar_ID_106017 Human_SNP_ID_307055076 m1A Human chr7 - 1445002 1445002 1445002 ATGGGCTGGTCGTCAGCTGCCCCGTGCACAGCAGCGGCTGCCTCCCATCCCGCCGTGCCCCCGAG ATGGGCTGGTCGTCAGCTGCCCCGTGCACAGCTGCGGCTGCCTCCCATCCCGCCGTGCCCCCGAG T A MICALL2 Ensembl:ENSG00000164877 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1444641..1445183 26863196 MeRIP-seq:(Medium) rs112939816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17092536,Human_RBP_ID_22110551 Human_miRNA_ID_2474899,Human_miRNA_ID_2960686 RMVar_hsa_circ_91852,RMVar_hsa_circ_243256,RMVar_hsa_circ_77886,RMVar_hsa_circ_243260 106018 RMVar_ID_106018 Human_SNP_ID_307056329 m1A Human chr7 + 1447623 1447623 1447623 CCCCCTGCACCCTCATTCCTCCTCTGGACCACAGGGTTTGTCTGGGCTGGAGATAGTGGAGGCTT CCCCCTGCACCCTCATTCCTCCTCTGGACCACGGGGTTTGTCTGGGCTGGAGATAGTGGAGGCTT A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1447541..1447706 26863196 MeRIP-seq:(Medium) rs755496457 Functional Loss SNV dbSNP153 33..33 33 - - - 106019 RMVar_ID_106019 Human_SNP_ID_307058174 m1A Human chr7 - 1452883 1452883 1452883 GGAGGGCCGGCCCTGGGGAAGGAGCTTGGGGCAGGATGGGTGGTGGCTGTGGGACCGGCCGGGGT GGAGGGCCGGCCCTGGGGAAGGAGCTTGGGGCGGGATGGGTGGTGGCTGTGGGACCGGCCGGGGT T C MICALL2 Ensembl:ENSG00000164877 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1452873..1452989 26863196 MeRIP-seq:(Medium) rs1283609022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14244,Human_RBP_ID_267573,Human_RBP_ID_3860312,Human_RBP_ID_5327711,Human_RBP_ID_8149085,Human_RBP_ID_8217610,Human_RBP_ID_8237662,Human_RBP_ID_9336931,Human_RBP_ID_9439157,Human_RBP_ID_17427253,Human_RBP_ID_18503478,Human_RBP_ID_22685107,Human_RBP_ID_22729096,Human_RBP_ID_26356143,Human_RBP_ID_27574463 106020 RMVar_ID_106020 Human_SNP_ID_307060385 m1A Human chr7 + 1459355 1459339 1459355 CCATGTGGGCGGCGCGCCCGCCGCGCGGCGGAACCGCCCTCCGACACCTTCCCGCGGCTGTGCCG CCATGTGGGCGGCGCGC________________CCGCCCTCCGACACCTTCCCGCGGCTGTGCCG CCCGCCGCGCGGCGGAA C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1459310..1459433 26863196 MeRIP-seq:(Medium) rs1275595309 Functional Loss DEL dbSNP153 18..33 33 - - - 106021 RMVar_ID_106021 Human_SNP_ID_307060548 m1A Human chr7 + 1459610 1459610 1459610 TAGGCCCCGTCCTCACACCTCCCAGCCCCGGCATAGGCTCCCGCCCAGGCAGGCCCCACCTCCCG TAGGCCCCGTCCTCACACCTCCCAGCCCCGGCGTAGGCTCCCGCCCAGGCAGGCCCCACCTCCCG A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1459607..1459725 26863196 MeRIP-seq:(Medium) rs1320706978 Functional Loss SNV dbSNP153 33..33 33 - - - 106022 RMVar_ID_106022 Human_SNP_ID_307060552 m1A Human chr7 + 1459635 1459614 1459636 CCCCGGCATAGGCTCCCGCCCAGGCAGGCCCCACCTCCCGACAGGCCCCGCCCCCAGCCGCCGGG CCCCGGCATAGG______________________CTCCCGACAGGCCCCGCCCCCAGCCGCCGGG GCTCCCGCCCAGGCAGGCCCCAC G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1459584..1459770 26863196 MeRIP-seq:(Medium) rs1433354132 Functional Loss DEL dbSNP153 13..34 33 - - - 106023 RMVar_ID_106023 Human_SNP_ID_307060562 m1A Human chr7 + 1459635 1459635 1459635 CCCCGGCATAGGCTCCCGCCCAGGCAGGCCCCACCTCCCGACAGGCCCCGCCCCCAGCCGCCGGG CCCCGGCATAGGCTCCCGCCCAGGCAGGCCCCCCCTCCCGACAGGCCCCGCCCCCAGCCGCCGGG A C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1459584..1459770 26863196 MeRIP-seq:(Medium) rs1306141442 Functional Loss SNV dbSNP153 33..33 33 - - - 106024 RMVar_ID_106024 Human_SNP_ID_307062897 m1A Human chr7 + 1466265 1466261 1466266 TGGGCCCAACTCCTCCCCACCGCTCAAGACCCAGCCCGCCATGCCACCTTCCCTCAACAGCCCTT TGGGCCCAACTCCTCCCCACCGCTCAAGA_____CCCGCCATGCCACCTTCCCTCAACAGCCCTT ACCCAG A RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1466216..1466327 26863196 MeRIP-seq:(Medium) rs1562477872 Functional Loss DEL dbSNP153 30..34 33 - - - 106025 RMVar_ID_106025 Human_SNP_ID_307062907 m1A Human chr7 + 1466278 1466278 1466278 TCCCCACCGCTCAAGACCCAGCCCGCCATGCCACCTTCCCTCAACAGCCCTTCCTAACTTCCACA TCCCCACCGCTCAAGACCCAGCCCGCCATGCCCCCTTCCCTCAACAGCCCTTCCTAACTTCCACA A C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1466227..1466344 26863196 MeRIP-seq:(Medium) rs765464696 Functional Loss SNV dbSNP153 33..33 33 - - - 106026 RMVar_ID_106026 Human_SNP_ID_307064357 m1A Human chr7 + 1470396 1470394 1470396 GAATGAGGGCTTGCTGGACGGCCCCTGATGCCAGCGGCCGGCCCGGAGCCACCCCAGGGCTCGGA GAATGAGGGCTTGCTGGACGGCCCCTGATGC__GCGGCCGGCCCGGAGCCACCCCAGGGCTCGGA CCA C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:1470301..1470550 26863410 MeRIP-seq:(Medium) rs1471115601 Functional Loss DEL dbSNP153 32..33 33 - - - 106027 RMVar_ID_106027 Human_SNP_ID_307064653 m1A Human chr7 - 1470949 1470949 1470949 CCCACTGAAGTGTGTGGGTCTTTCAGCATTGCAGCCGCTTTCCTGCCCACGTTCATGTACTGCCT CCCACTGAAGTGTGTGGGTCTTTCAGCATTGCGGCCGCTTTCCTGCCCACGTTCATGTACTGCCT T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1470840..1470983 26863196 MeRIP-seq:(Medium) rs773020115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837694,Human_Splice_Rec_837704 RMVar_hsa_circ_117445,RMVar_hsa_circ_101523,RMVar_hsa_circ_102524,RMVar_hsa_circ_125798,RMVar_hsa_circ_243262,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243263,RMVar_hsa_circ_243261,RMVar_hsa_circ_28086,RMVar_hsa_circ_104277,RMVar_hsa_circ_243265,RMVar_hsa_circ_243266 106028 RMVar_ID_106028 Human_SNP_ID_307064655 m1A Human chr7 + 1470952 1470952 1470952 CAGTACATGAACGTGGGCAGGAAAGCGGCTGCAATGCTGAAAGACCCACACACTTCAGTGGGAAC CAGTACATGAACGTGGGCAGGAAAGCGGCTGCTATGCTGAAAGACCCACACACTTCAGTGGGAAC A T RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:1470826..1470975 26863196 MeRIP-seq:(Medium) rs1439698965 Functional Loss SNV dbSNP153 33..33 33 - - - 106029 RMVar_ID_106029 Human_SNP_ID_307064735 m1A Human chr7 - 1471140 1471140 1471140 CCTTCAGCCTGGCCCTGCGCTCCATGCAGAACAGCCCCAGGTGAGGCCACCGCCGGCCTCTGTCC CCTTCAGCCTGGCCCTGCGCTCCATGCAGAACGGCCCCAGGTGAGGCCACCGCCGGCCTCTGTCC T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:1471126..1471225 26863196 MeRIP-seq:(Medium) rs759308683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837692,Human_Splice_Rec_837693,Human_Splice_Rec_837702,Human_Splice_Rec_837703,Human_Splice_Rec_837712,Human_Splice_Rec_837714 RMVar_hsa_circ_117445,RMVar_hsa_circ_101523,RMVar_hsa_circ_102524,RMVar_hsa_circ_125798,RMVar_hsa_circ_243262,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243263,RMVar_hsa_circ_243261,RMVar_hsa_circ_105663,RMVar_hsa_circ_104277,RMVar_hsa_circ_243265,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_243267 106030 RMVar_ID_106030 Human_SNP_ID_307068153 m1A Human chr7 + 1478455 1478455 1478455 TGACGGCACGGACGGTGGAGCTGACCACCTCCAGGTCCTGACGGAAGGCCAGGGCCTCGGCCAGG TGACGGCACGGACGGTGGAGCTGACCACCTCCTGGTCCTGACGGAAGGCCAGGGCCTCGGCCAGG A T RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1478405..1478490 26863196 MeRIP-seq:(Medium) rs1453164826 Functional Loss SNV dbSNP153 33..33 33 - - - 106031 RMVar_ID_106031 Human_SNP_ID_307069161 m1A Human chr7 - 1480800 1480800 1480800 ACTGGGGAGGGGTGGGGCCAGCACAGAGACCCAGCCTGGGGAGGGGTGGGGCCAACACAGAGACC ACTGGGGAGGGGTGGGGCCAGCACAGAGACCCGGCCTGGGGAGGGGTGGGGCCAACACAGAGACC T C INTS1 Ensembl:ENSG00000164880 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1480796..1480933 26863196 MeRIP-seq:(Medium) rs1368369808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26794194 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_116928,RMVar_hsa_circ_82523,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243273,RMVar_hsa_circ_243274,RMVar_hsa_circ_265365,RMVar_hsa_circ_243276 106032 RMVar_ID_106032 Human_SNP_ID_307070354 m1A Human chr7 + 1483768 1483768 1483768 GCTCACCTCGAGGCGGGCCCAGCGTCAGCAGGATCACCATGGCATGGACCACGAGGATGTGCATG GCTCACCTCGAGGCGGGCCCAGCGTCAGCAGGGTCACCATGGCATGGACCACGAGGATGTGCATG A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:1483738..1485350 32194978 MeRIP-seq:(Medium) rs765652740 Functional Loss SNV dbSNP153 33..33 33 - - - 106033 RMVar_ID_106033 Human_SNP_ID_307071105 m1A Human chr7 - 1485399 1485399 1485399 CGGGGAGGAGAAGGAGCCCCCCATGGAGGAGGATGTGGGGGACACAGATGTGCTGCAGGGCTATC CGGGGAGGAGAAGGAGCCCCCCATGGAGGAGGGTGTGGGGGACACAGATGTGCTGCAGGGCTATC T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1485348..1485507 26863196 MeRIP-seq:(Medium) rs1480396830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14254,Human_RBP_ID_21993683 Human_Splice_Rec_837648,Human_Splice_Rec_837734 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_34648,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_120522,RMVar_hsa_circ_36665,RMVar_hsa_circ_243280,RMVar_hsa_circ_243281,RMVar_hsa_circ_243282 106034 RMVar_ID_106034 Human_SNP_ID_307071109 m1A Human chr7 - 1485402 1485402 1485402 GGACGGGGAGGAGAAGGAGCCCCCCATGGAGGAGGATGTGGGGGACACAGATGTGCTGCAGGGCT GGACGGGGAGGAGAAGGAGCCCCCCATGGAGGCGGATGTGGGGGACACAGATGTGCTGCAGGGCT T G INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1485352..1485503 26863196 MeRIP-seq:(Medium) rs550057502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14254,Human_RBP_ID_21993683 Human_Splice_Rec_837648,Human_Splice_Rec_837734 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_34648,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_120522,RMVar_hsa_circ_36665,RMVar_hsa_circ_243280,RMVar_hsa_circ_243281,RMVar_hsa_circ_243282 106035 RMVar_ID_106035 Human_SNP_ID_307071120 m1A Human chr7 - 1485421 1485421 1485421 TTTCGGAGGGCAGCCTGCGGGACGGGGAGGAGAAGGAGCCCCCCATGGAGGAGGATGTGGGGGAC TTTCGGAGGGCAGCCTGCGGGACGGGGAGGAGCAGGAGCCCCCCATGGAGGAGGATGTGGGGGAC T G INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1485071..1485497 26863196 MeRIP-seq:(Medium) rs769105615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8914845,Human_RBP_ID_22834191 Human_Splice_Rec_837648,Human_Splice_Rec_837734 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_34648,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_120522,RMVar_hsa_circ_36665,RMVar_hsa_circ_243280,RMVar_hsa_circ_243281,RMVar_hsa_circ_243282 106036 RMVar_ID_106036 Human_SNP_ID_307071810 m1A Human chr7 - 1486971 1486971 1486971 GCACGATGCTGTGGACGATGCTGCTTCCGGGGAGGAGGACGACGAGGGCGAGAGCAAGGAGCAGA GCACGATGCTGTGGACGATGCTGCTTCCGGGGGGGAGGACGACGAGGGCGAGAGCAAGGAGCAGA T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1486894..1487032 26863196 MeRIP-seq:(Medium) rs771446189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843496,Human_RBP_ID_7714489 Human_Splice_Rec_837645,Human_Splice_Rec_837731 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_34648,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_120522,RMVar_hsa_circ_36665,RMVar_hsa_circ_243280,RMVar_hsa_circ_243281,RMVar_hsa_circ_243283,RMVar_hsa_circ_243282,RMVar_hsa_circ_274467,RMVar_hsa_circ_102384,RMVar_hsa_circ_243284 106037 RMVar_ID_106037 Human_SNP_ID_307073018 m1A Human chr7 - 1489641 1489641 1489641 TCCGAACCTCGCCATCTCTACCCTCTACTGGAAGGCCTGGCCCCTCCTGCTGGTCGTCGCCGCAT TCCGAACCTCGCCATCTCTACCCTCTACTGGAGGGCCTGGCCCCTCCTGCTGGTCGTCGCCGCAT T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1489554..1489710 26863196 MeRIP-seq:(Medium) rs1263710462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837636,Human_Splice_Rec_837637,Human_Splice_Rec_837722,Human_Splice_Rec_837723 RMVar_hsa_circ_117445,RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_243266,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_6637,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_34648,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_120522,RMVar_hsa_circ_243280,RMVar_hsa_circ_243281,RMVar_hsa_circ_81415,RMVar_hsa_circ_243283,RMVar_hsa_circ_243282,RMVar_hsa_circ_274467,RMVar_hsa_circ_102384,RMVar_hsa_circ_243284,RMVar_hsa_circ_243285,RMVar_hsa_circ_360979,RMVar_hsa_circ_243286,RMVar_hsa_circ_370471,RMVar_hsa_circ_266356 106038 RMVar_ID_106038 Human_SNP_ID_307074217 m1A Human chr7 - 1492885 1492885 1492885 TCCCGCCCGGGTAAGCCTGCGCCCCGCTCCCCACTCCCGCCCGGGTAAGCCCGCGCCCCGCTCCC TCCCGCCCGGGTAAGCCTGCGCCCCGCTCCCCCCTCCCGCCCGGGTAAGCCCGCGCCCCGCTCCC T G INTS1 Ensembl:ENSG00000164880 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1492881..1493030 26863196 MeRIP-seq:(Medium) rs1237546999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5328241 RMVar_hsa_circ_243264,RMVar_hsa_circ_83582,RMVar_hsa_circ_124376,RMVar_hsa_circ_243268,RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_6637,RMVar_hsa_circ_116928,RMVar_hsa_circ_77646,RMVar_hsa_circ_120082,RMVar_hsa_circ_243270,RMVar_hsa_circ_243271,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_114821,RMVar_hsa_circ_243276,RMVar_hsa_circ_124444,RMVar_hsa_circ_243277,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279,RMVar_hsa_circ_96528,RMVar_hsa_circ_13009,RMVar_hsa_circ_112897,RMVar_hsa_circ_243281,RMVar_hsa_circ_81415,RMVar_hsa_circ_243282,RMVar_hsa_circ_102384,RMVar_hsa_circ_243284,RMVar_hsa_circ_243285,RMVar_hsa_circ_360979,RMVar_hsa_circ_266356 106039 RMVar_ID_106039 Human_SNP_ID_307077740 m1A Human chr7 - 1500309 1500309 1500309 GATCGAGGCGGCCGAGCTGGAGGGCAACGATGACAGGATCGAGGGCGTGCTGTGCGGGGCCGTGA GATCGAGGCGGCCGAGCTGGAGGGCAACGATGGCAGGATCGAGGGCGTGCTGTGCGGGGCCGTGA T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1500259..1500326 26863196 MeRIP-seq:(Medium) rs747527315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793811,Human_RBP_ID_953030,Human_RBP_ID_16079611,Human_RBP_ID_19020463 Human_Splice_Rec_837610,Human_Splice_Rec_837748 RMVar_hsa_circ_87927,RMVar_hsa_circ_243269,RMVar_hsa_circ_6637,RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_114821,RMVar_hsa_circ_243278,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279 106040 RMVar_ID_106040 Human_SNP_ID_307078837 m1A Human chr7 - 1503022 1503022 1503022 TCCAGTGCCTCGGCCCTCACCGGTCTCACCAAACGCCCCAAACTCTCCTCCACACCCCCTCTGAG TCCAGTGCCTCGGCCCTCACCGGTCTCACCAAGCGCCCCAAACTCTCCTCCACACCCCCTCTGAG T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1502971..1503217 26863196 MeRIP-seq:(Medium) rs1466403937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175228,Human_RBP_ID_22320102,Human_RBP_ID_27529944 Human_miRNA_ID_2369598,Human_miRNA_ID_2705880 RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279 106041 RMVar_ID_106041 Human_SNP_ID_307078840 m1A Human chr7 - 1503027 1503027 1503027 CGTTGTCCAGTGCCTCGGCCCTCACCGGTCTCACCAAACGCCCCAAACTCTCCTCCACACCCCCT CGTTGTCCAGTGCCTCGGCCCTCACCGGTCTCGCCAAACGCCCCAAACTCTCCTCCACACCCCCT T C INTS1 Ensembl:ENSG00000164880 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:1503001..1503200 26863196 MeRIP-seq:(Medium) rs200053969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175228,Human_RBP_ID_27529944 RMVar_hsa_circ_118319,RMVar_hsa_circ_243272,RMVar_hsa_circ_92745,RMVar_hsa_circ_243274,RMVar_hsa_circ_103716,RMVar_hsa_circ_243279 106042 RMVar_ID_106042 Human_SNP_ID_307081524 m1A Human chr7 - 1509352 1509352 1509352 TGGGGCTGGGACGGGGCGAACAGTGGCCCCATAGCCCACGTCCACCGGAGCCACAGGATGGGAGC TGGGGCTGGGACGGGGCGAACAGTGGCCCCATGGCCCACGTCCACCGGAGCCACAGGATGGGAGC T C AC093734.1 Ensembl:ENSG00000231927 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1509348..1509450 26863196 MeRIP-seq:(Medium) rs917423541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837753 106043 RMVar_ID_106043 Human_SNP_ID_307081552 m1A Human chr7 + 1509415 1509415 1509415 CACGCCGAGGACTGCCGGGTCCTGCAGGGTCTACATCTCCGTCTCACCTCCCCCGATGCCGCCCC CACGCCGAGGACTGCCGGGTCCTGCAGGGTCTGCATCTCCGTCTCACCTCCCCCGATGCCGCCCC A G RF00017-4503,RF00017-4541,L13304-001,L13705-009,lnc-MAFK-6 RNACentral:URS00009569F7,RNACentral:URS0000992647,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS0000D57654 SRP RNA,SRP RNA,scRNA,misc_RNA,lincRNA intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1509413..1509526 26863196 MeRIP-seq:(Medium) rs1236514777 Functional Loss SNV dbSNP153 33..33 33 - - - 106044 RMVar_ID_106044 Human_SNP_ID_307088440 m1A Human chr7 - 1530761 1530759 1530762 GGCGCTCGGGCTCCGACTTCGCGAAGAACAACAAGTGCCCCCGCGCCGCCCGCCGCCACCGCACC GGCGCTCGGGCTCCGACTTCGCGAAGAACAA___GTGCCCCCGCGCCGCCCGCCGCCACCGCACC CTTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1530701..1537500 26863196 MeRIP-seq:(Medium) rs1007220732 Functional Loss DEL dbSNP153 32..34 33 - - - 106045 RMVar_ID_106045 Human_SNP_ID_307089306 m1A Human chr7 - 1533194 1533194 1533194 CAGTGCGGAGAAGCAGGAAGGCTCTACACCAGACCCCACCGGCCTGTGGGACAGGCCAGCAGACC CAGTGCGGAGAAGCAGGAAGGCTCTACACCAGCCCCCACCGGCCTGTGGGACAGGCCAGCAGACC T G LOC100128653 RNACentral:URS0000BC44C9 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:1533188..1533450 32194978 MeRIP-seq:(Medium) rs1454641429 Functional Loss SNV dbSNP153 33..33 33 - - - 106046 RMVar_ID_106046 Human_SNP_ID_307091127 m1A Human chr7 + 1538193 1538193 1538193 CCATGGCAACTATCGGAGGGCTCATGCCGGGGATGCTTTGGCTGGGTTTTTCATGAATGATTAGA CCATGGCAACTATCGGAGGGCTCATGCCGGGGGTGCTTTGGCTGGGTTTTTCATGAATGATTAGA A G MAFK Ensembl:ENSG00000198517 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1538183..1538481 26863196 MeRIP-seq:(Medium) rs1186770662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24204032,Human_RBP_ID_26090176 Human_miRNA_ID_931729 106047 RMVar_ID_106047 Human_SNP_ID_307091222 m1A Human chr7 - 1538413 1538413 1538413 CGCTGCGGCTGTGACATCACCACCTCCACCTAAGCTGCCCCCGAGCGAGGACCCTGCGGCCCAAG CGCTGCGGCTGTGACATCACCACCTCCACCTAGGCTGCCCCCGAGCGAGGACCCTGCGGCCCAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1538408..1538496 26863196 MeRIP-seq:(Medium) rs897358267 Functional Loss SNV dbSNP153 33..33 33 - - - 106048 RMVar_ID_106048 Human_SNP_ID_307091760 m1A Human chr7 + 1539926 1539926 1539926 GACACCCCACGTTCTCCCGCCGCTGACCCCGCACTGTGGCCCCCCAGGTCAAGAAGGAGGCGGGC GACACCCCACGTTCTCCCGCCGCTGACCCCGCGCTGTGGCCCCCCAGGTCAAGAAGGAGGCGGGC A G MAFK Ensembl:ENSG00000198517 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:1539921..1540305;chr7:1539920..1540272 26863196 MeRIP-seq:(Medium) rs1217915603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22871 106049 RMVar_ID_106049 Human_SNP_ID_307092440 m1A Human chr7 - 1541427 1541427 1541427 CGCAACGTCCTCCTCCTTCCACCTCCACATCCATGTCCACCAACATCCCCCAGGCTGCACCCCCT CGCAACGTCCTCCTCCTTCCACCTCCACATCCGTGTCCACCAACATCCCCCAGGCTGCACCCCCT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:1541376..1541600 26863196 MeRIP-seq:(Medium) rs948839351 Functional Loss SNV dbSNP153 33..33 33 - - - 106050 RMVar_ID_106050 Human_SNP_ID_307092884 m1A Human chr7 + 1542807 1542800 1542808 AGGGCGTGGGGACCCCGGCCCCCTATGCCGCCACGCCGCCACACCGCCTCACCCTGGCTTCTGTG AGGGCGTGGGGACCCCGGCCCCCTAT________GCCGCCACACCGCCTCACCCTGGCTTCTGTG TGCCGCCAC T MAFK Ensembl:ENSG00000198517 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1542640..1543000 26863196 MeRIP-seq:(Medium) rs1051038467 Functional Loss DEL dbSNP153 27..34 33 - - - 106051 RMVar_ID_106051 Human_SNP_ID_307093512 m1A Human chr7 + 1544526 1544526 1544526 AACCCCTTTTTTAGCAGCGATGACGACACTGGAACCACGCTAGTCTCCGTCCCTCCCGCTCACAT AACCCCTTTTTTAGCAGCGATGACGACACTGGGACCACGCTAGTCTCCGTCCCTCCCGCTCACAT A G L13304-001,L13705-009,lnc-ELFN1-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00009AFF67 scRNA,misc_RNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1544475..1544563 26863196 MeRIP-seq:(Medium) rs958415975 Functional Loss SNV dbSNP153 33..33 33 - - - 106052 RMVar_ID_106052 Human_SNP_ID_307093885 m1A Human chr7 - 1545708 1545708 1545708 CTTCTGGGAGGACACACGGCTGGCCCAGGGCGAGGGGTGTCACTGCAGGGCGCCCCCCAGGCCCA CTTCTGGGAGGACACACGGCTGGCCCAGGGCGGGGGGTGTCACTGCAGGGCGCCCCCCAGGCCCA T C TMEM184A Ensembl:ENSG00000164855 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1545415..1545814 26863196 MeRIP-seq:(Medium) rs1264566559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27530280 106053 RMVar_ID_106053 Human_SNP_ID_307094708 m1A Human chr7 - 1547751 1547751 1547751 TCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGAATTCACCAGGTACACCCTGCCTTCCAGCTGGG TCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGGATTCACCAGGTACACCCTGCCTTCCAGCTGGG T C TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1546930..1547865 26863196 MeRIP-seq:(Medium) rs920137344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837783,Human_Splice_Rec_837799,Human_Splice_Rec_837811 106054 RMVar_ID_106054 Human_SNP_ID_307094710 m1A Human chr7 - 1547756 1547754 1547757 TGCCTTCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGAATTCACCAGGTACACCCTGCCTTCCAG TGCCTTCCCCTGCCAGGTGTACGCAGAGAAG___GAGAATTCACCAGGTACACCCTGCCTTCCAG CCTT C TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1546932..1547831 26863196 MeRIP-seq:(Medium) rs548246825 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_837783,Human_Splice_Rec_837799,Human_Splice_Rec_837811 106055 RMVar_ID_106055 Human_SNP_ID_307094713 m1A Human chr7 - 1547756 1547756 1547756 TGCCTTCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGAATTCACCAGGTACACCCTGCCTTCCAG TGCCTTCCCCTGCCAGGTGTACGCAGAGAAGAGGGAGAATTCACCAGGTACACCCTGCCTTCCAG T C TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1546932..1547831 26863196 MeRIP-seq:(Medium) rs780897295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837783,Human_Splice_Rec_837799,Human_Splice_Rec_837811 106056 RMVar_ID_106056 Human_SNP_ID_307095117 m1A Human chr7 + 1548654 1548654 1548654 GGCGTAGAGGGCGAGGCTGACGGAGGCGTTGTAGATGAGGGTCACATAGAGGTAGCCGCTGCGGA GGCGTAGAGGGCGAGGCTGACGGAGGCGTTGTGGATGAGGGTCACATAGAGGTAGCCGCTGCGGA A G L13304-001,L13705-009,lnc-ELFN1-4,NONHSAG046773.2 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00009AFF67,RNACentral:URS00008BD08C scRNA,misc_RNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1548603..1548688 26863196 MeRIP-seq:(Medium) rs1267017558 Functional Loss SNV dbSNP153 33..33 33 - - - 106057 RMVar_ID_106057 Human_SNP_ID_307096189 m1A Human chr7 - 1550941 1550939 1550942 CACCTGCGCTCCTACACCGTGCCACAGGAGCAACGTTACATCATCCGCCTGCTCCTCATCGTGCC CACCTGCGCTCCTACACCGTGCCACAGGAGC___GTTACATCATCCGCCTGCTCCTCATCGTGCC CGTT C TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1550892..1551132 26863196 MeRIP-seq:(Medium) rs1205170708 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_837772,Human_Splice_Rec_837790,Human_Splice_Rec_837816,Human_Splice_Rec_837828,Human_Splice_Rec_837838,Human_Splice_Rec_837846,Human_Splice_Rec_837854,Human_Splice_Rec_837860 106058 RMVar_ID_106058 Human_SNP_ID_307097638 m1A Human chr7 - 1555366 1555366 1555366 GCCAGCTGGGCCGCAGATGGACCACATGGGGAACAGCTCCCAGGGGGCCCCCTGGCTCTTCCTCA GCCAGCTGGGCCGCAGATGGACCACATGGGGATCAGCTCCCAGGGGGCCCCCTGGCTCTTCCTCA T A TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1555317..1555500 26863196 MeRIP-seq:(Medium) rs200512714 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 106059 RMVar_ID_106059 Human_SNP_ID_307101543 m1A Human chr7 - 1567574 1567574 1567574 AGGGAGGAACTTTGGCACTAGCCCTTGGAGCCAGGAAAAAAGACTCGTGTCTCAGGCAGACTCTT AGGGAGGAACTTTGGCACTAGCCCTTGGAGCCCGGAAAAAAGACTCGTGTCTCAGGCAGACTCTT T G PSMG3 Ensembl:ENSG00000157778 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:1567526..1567707 26863196 MeRIP-seq:(Medium) rs926617151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_680482,Human_RBP_ID_1684682,Human_RBP_ID_2039180,Human_RBP_ID_5123391,Human_RBP_ID_9208701,Human_RBP_ID_27530328 Human_miRNA_ID_338324,Human_miRNA_ID_2082916,Human_miRNA_ID_2082917 RMVar_hsa_circ_80939,RMVar_hsa_circ_119443,RMVar_hsa_circ_84420,RMVar_hsa_circ_243292,RMVar_hsa_circ_243294,RMVar_hsa_circ_76489,RMVar_hsa_circ_243293,RMVar_hsa_circ_243291 106060 RMVar_ID_106060 Human_SNP_ID_307101573 m1A Human chr7 + 1567672 1567672 1567672 AGTGGGTGTCTGGGTGTTCACGTGTCCTGCTGAGCAGCGCGGGGCGGCTGCCTCCAGGTCACCAC AGTGGGTGTCTGGGTGTTCACGTGTCCTGCTGGGCAGCGCGGGGCGGCTGCCTCCAGGTCACCAC A G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:1567623..1567722 32194978 MeRIP-seq:(Medium) rs770773058 Functional Loss SNV dbSNP153 33..33 33 - - - 106061 RMVar_ID_106061 Human_SNP_ID_307102072 m1A Human chr7 + 1569143 1569143 1569143 CAATCCACTTTACCTCATCCTGCCCCAGAAGGACTTTTGTGGTGAGCACAGGCTTGCTGACGTCA CAATCCACTTTACCTCATCCTGCCCCAGAAGGTCTTTTGTGGTGAGCACAGGCTTGCTGACGTCA A T L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1567819..1569191 32194978 MeRIP-seq:(Medium) rs1404958931 Functional Loss SNV dbSNP153 33..33 33 - - - 106062 RMVar_ID_106062 Human_SNP_ID_307102111 m1A Human chr7 - 1569255 1569255 1569255 GGGTCCCCACCCAGGTGGTGTGTACGGCCTTCAGCAGTCACATCCTGGTGGTGGTGACCCAGTTT GGGTCCCCACCCAGGTGGTGTGTACGGCCTTCGGCAGTCACATCCTGGTGGTGGTGACCCAGTTT T C PSMG3 Ensembl:ENSG00000157778 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1569212..1569454 26863196 MeRIP-seq:(Medium) rs750524295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13640,Human_RBP_ID_680496,Human_RBP_ID_4934361,Human_RBP_ID_26091322 RMVar_hsa_circ_80939,RMVar_hsa_circ_84420,RMVar_hsa_circ_243292,RMVar_hsa_circ_243294,RMVar_hsa_circ_76489,RMVar_hsa_circ_243293,RMVar_hsa_circ_326015 106063 RMVar_ID_106063 Human_SNP_ID_307102171 m1A Human chr7 + 1569359 1569359 1569359 GCGTGTCTTCCATGGCGGGGCTCTGCAGTGGCAGCTTTAATTTAGGTTAAAAAGAAAGGGGAAAA GCGTGTCTTCCATGGCGGGGCTCTGCAGTGGCGGCTTTAATTTAGGTTAAAAAGAAAGGGGAAAA A G L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:1569326..1569565 26863196 MeRIP-seq:(Medium) rs201644540 Functional Loss SNV dbSNP153 33..33 33 - - - 106064 RMVar_ID_106064 Human_SNP_ID_307210127 m1A Human chr7 - 1898351 1898351 1898351 GAAGCAGGTGGAGAGTGCCGAGCTGAAGAACCAGCGGCTCAAGGAGGTTTTCCAGACCAAGATCC GAAGCAGGTGGAGAGTGCCGAGCTGAAGAACCTGCGGCTCAAGGAGGTTTTCCAGACCAAGATCC T A MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1898301..1898350 32194978 MeRIP-seq:(Medium) rs1193808551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837972,Human_Splice_Rec_838004,Human_Splice_Rec_838040,Human_Splice_Rec_838076,Human_Splice_Rec_838092,Human_Splice_Rec_838098,Human_Splice_Rec_838226 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_276759,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_243297 106065 RMVar_ID_106065 Human_SNP_ID_307222066 m1A Human chr7 + 1931074 1931074 1931074 ACACCACGGGAACACCCCCAACTCCTCACCCCACCCACGGTCACAGGAGCGAGGGCGCATCATGG ACACCACGGGAACACCCCCAACTCCTCACCCCCCCCACGGTCACAGGAGCGAGGGCGCATCATGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1931072..1931158 26863196 MeRIP-seq:(Medium) rs948603964 Functional Loss SNV dbSNP153 33..33 33 - - - 106066 RMVar_ID_106066 Human_SNP_ID_307224035 m1A Human chr7 - 1936754 1936754 1936754 CGACTGCGCGGGCTCCTGCGCGCCATGGAGAGAGGAGGCACCGTCCCAGCCGACCTTGAGGCTGC CGACTGCGCGGGCTCCTGCGCGCCATGGAGAGGGGAGGCACCGTCCCAGCCGACCTTGAGGCTGC T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:1936667..1940139 26863196 MeRIP-seq:(Medium) rs1054128157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_837971,Human_Splice_Rec_838003,Human_Splice_Rec_838039,Human_Splice_Rec_838075,Human_Splice_Rec_838091,Human_Splice_Rec_838097,Human_Splice_Rec_838225 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_307181,RMVar_hsa_circ_333067,RMVar_hsa_circ_348537,RMVar_hsa_circ_320685,RMVar_hsa_circ_299068 106067 RMVar_ID_106067 Human_SNP_ID_307224064 m1A Human chr7 - 1936788 1936788 1936788 CGAGGACCACAGCCAGCTGCAGGCGGAGTGCGAGCGACTGCGCGGGCTCCTGCGCGCCATGGAGA CGAGGACCACAGCCAGCTGCAGGCGGAGTGCGGGCGACTGCGCGGGCTCCTGCGCGCCATGGAGA T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1936699..1940139 26863196 MeRIP-seq:(Medium) rs1316932400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26830100 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_307181,RMVar_hsa_circ_333067,RMVar_hsa_circ_348537,RMVar_hsa_circ_320685,RMVar_hsa_circ_299068 106068 RMVar_ID_106068 Human_SNP_ID_307224070 m1A Human chr7 - 1936794 1936794 1936794 CCTGCGCGAGGACCACAGCCAGCTGCAGGCGGAGTGCGAGCGACTGCGCGGGCTCCTGCGCGCCA CCTGCGCGAGGACCACAGCCAGCTGCAGGCGGTGTGCGAGCGACTGCGCGGGCTCCTGCGCGCCA T A MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1936743..1936943 26863196 MeRIP-seq:(Medium) rs1345740834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26830100 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_307181,RMVar_hsa_circ_333067,RMVar_hsa_circ_348537,RMVar_hsa_circ_320685,RMVar_hsa_circ_299068 106069 RMVar_ID_106069 Human_SNP_ID_307224071 m1A Human chr7 - 1936794 1936794 1936794 CCTGCGCGAGGACCACAGCCAGCTGCAGGCGGAGTGCGAGCGACTGCGCGGGCTCCTGCGCGCCA CCTGCGCGAGGACCACAGCCAGCTGCAGGCGGCGTGCGAGCGACTGCGCGGGCTCCTGCGCGCCA T G MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1936743..1936943 26863196 MeRIP-seq:(Medium) rs1345740834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26830100 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_307181,RMVar_hsa_circ_333067,RMVar_hsa_circ_348537,RMVar_hsa_circ_320685,RMVar_hsa_circ_299068 106070 RMVar_ID_106070 Human_SNP_ID_307231682 m1A Human chr7 + 1957717 1957717 1957717 GACTCCGCTCGCCTTCCAGCTCCTCGACCTTCAACCTGCAAGGACAGCAAGACGGTGACCAGGTG GACTCCGCTCGCCTTCCAGCTCCTCGACCTTCTACCTGCAAGGACAGCAAGACGGTGACCAGGTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:1957666..1980678 32194978 MeRIP-seq:(Medium) rs1348167573 Functional Loss SNV dbSNP153 33..33 33 - - - 106071 RMVar_ID_106071 Human_SNP_ID_307255984 m1A Human chr7 + 2036960 2036938 2036961 CGCCTCCTGAACACTCCTCCCAGGGCTCCTCCAGCACTCCTCCCACAGCTCCCCCCACAGCACGA CGCCTCCTGAA_______________________CACTCCTCCCACAGCTCCCCCCACAGCACGA ACACTCCTCCCAGGGCTCCTCCAG A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2036950..2037036 26863196 MeRIP-seq:(Medium) rs1403387320 Functional Loss DEL dbSNP153 12..34 33 - - - 106072 RMVar_ID_106072 Human_SNP_ID_307274141 m1A Human chr7 - 2092437 2092437 2092437 CAGTCAACCGATATCCAGAGGGCAGATGCGTGAGGGAGGATGCTTGGGTGGGGCGTGGTCATGCA CAGTCAACCGATATCCAGAGGGCAGATGCGTGGGGGAGGATGCTTGGGTGGGGCGTGGTCATGCA T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2092435..2092665 26863196 MeRIP-seq:(Medium) rs142484440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5502,RMVar_hsa_circ_35874,RMVar_hsa_circ_339649,RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_24626,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_38270,RMVar_hsa_circ_281224 106073 RMVar_ID_106073 Human_SNP_ID_307274181 m1A Human chr7 + 2092510 2092510 2092510 ACCACGCCCCGCCTAAGCATCCTCCCTCACACACCTGCCCTCTGGATATCGGTGACTGTGTTTTC ACCACGCCCCGCCTAAGCATCCTCCCTCACACGCCTGCCCTCTGGATATCGGTGACTGTGTTTTC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:2092416..2092612 26863196 MeRIP-seq:(Medium) rs1344724539 Functional Loss SNV dbSNP153 33..33 33 - - - 106074 RMVar_ID_106074 Human_SNP_ID_307278991 m1A Human chr7 - 2107404 2107404 2107404 AAGTGTGTCGGTGCGTGAGGATGCAGGGGTCCAGCGAAGAGGCTGTGGGTAGTTCAGGGGGAGGT AAGTGTGTCGGTGCGTGAGGATGCAGGGGTCCGGCGAAGAGGCTGTGGGTAGTTCAGGGGGAGGT T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2107399..2107675 26863196 MeRIP-seq:(Medium) rs1271839007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5502,RMVar_hsa_circ_35874,RMVar_hsa_circ_339649,RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_24626,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_38270,RMVar_hsa_circ_281224 106075 RMVar_ID_106075 Human_SNP_ID_307279423 m1A Human chr7 + 2109053 2109047 2109053 GCCTCCCTGTGCTGCGCACACAGCCTCCCCGCACCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA GCCTCCCTGTGCTGCGCACACAGCCTC______CCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA CCCCGCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2109047..2109117 26863196 MeRIP-seq:(Medium) rs1460903843 Functional Loss DEL dbSNP153 28..33 33 - - - 106076 RMVar_ID_106076 Human_SNP_ID_307279426 m1A Human chr7 + 2109053 2109053 2109053 GCCTCCCTGTGCTGCGCACACAGCCTCCCCGCACCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA GCCTCCCTGTGCTGCGCACACAGCCTCCCCGCGCCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2109047..2109117 26863196 MeRIP-seq:(Medium) rs1468743973 Functional Loss SNV dbSNP153 33..33 33 - - - 106077 RMVar_ID_106077 Human_SNP_ID_307279427 m1A Human chr7 + 2109053 2109053 2109053 GCCTCCCTGTGCTGCGCACACAGCCTCCCCGCACCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA GCCTCCCTGTGCTGCGCACACAGCCTCCCCGCTCCCGCTCTGCAGCTCAGAGCTGCTCACCCTCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2109047..2109117 26863196 MeRIP-seq:(Medium) rs1468743973 Functional Loss SNV dbSNP153 33..33 33 - - - 106078 RMVar_ID_106078 Human_SNP_ID_307281390 m1A Human chr7 - 2115431 2115431 2115431 TGACCCCGGAACACGCGGGGACCCTGTCCAGCACCTCCTCTGACCCCAGAACACGTGGGGACCCT TGACCCCGGAACACGCGGGGACCCTGTCCAGCGCCTCCTCTGACCCCAGAACACGTGGGGACCCT T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:2115404..2115555 26863196 MeRIP-seq:(Medium) rs553908998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3862005 RMVar_hsa_circ_5502,RMVar_hsa_circ_35874,RMVar_hsa_circ_339649,RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_24626,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_38270,RMVar_hsa_circ_281224 106079 RMVar_ID_106079 Human_SNP_ID_307288682 m1A Human chr7 + 2139408 2139407 2139408 CGGGCCCCAGGACGCACACTGAGATGCCCCCCACCCTCAGCAGTGAAGGTGACTCCCCCAGCCAT CGGGCCCCAGGACGCACACTGAGATGCCCCCC_CCCTCAGCAGTGAAGGTGACTCCCCCAGCCAT CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2139403..2139468 26863196 MeRIP-seq:(Medium) rs1202329169 Functional Loss DEL dbSNP153 33..33 33 - - - 106080 RMVar_ID_106080 Human_SNP_ID_307291503 m1A Human chr7 + 2148621 2148621 2148621 CTGGATGGCCCCTCACAGCCACGAGCGAAACCAGAGAAGAGCCGGGCTGTGGGATAAGAAGAAAT CTGGATGGCCCCTCACAGCCACGAGCGAAACCGGAGAAGAGCCGGGCTGTGGGATAAGAAGAAAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:2148619..2175171 26863196 MeRIP-seq:(Medium) rs1202958177 Functional Loss SNV dbSNP153 33..33 33 - - - 106081 RMVar_ID_106081 Human_SNP_ID_307306282 m1A Human chr7 - 2197866 2197866 2197866 CCGGGGGCTAGGACCAGTTTTGGCTCTCAGGCAGGGAGGGGTTGTGAACTCTGTTTTGGGAATGT CCGGGGGCTAGGACCAGTTTTGGCTCTCAGGCCGGGAGGGGTTGTGAACTCTGTTTTGGGAATGT T G MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2197861..2197975 26863196 MeRIP-seq:(Medium) rs927851681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7723207,Human_RBP_ID_8150300,Human_RBP_ID_8237844,Human_RBP_ID_16110617,Human_RBP_ID_17170146 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_101973,RMVar_hsa_circ_38270,RMVar_hsa_circ_318575,RMVar_hsa_circ_343244,RMVar_hsa_circ_268090,RMVar_hsa_circ_243307 106082 RMVar_ID_106082 Human_SNP_ID_307311146 m1A Human chr7 + 2213269 2213269 2213269 CCAGTCTCTCCCAGCTTTGCAGCTTGGCCAGCAGCCTCTGAAAAGACAACAAAAGCACAGACCCT CCAGTCTCTCCCAGCTTTGCAGCTTGGCCAGCCGCCTCTGAAAAGACAACAAAAGCACAGACCCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2213172..2213331 26863196 MeRIP-seq:(Medium) rs774993639 Functional Loss SNV dbSNP153 33..33 33 - - - 106083 RMVar_ID_106083 Human_SNP_ID_307312065 m1A Human chr7 - 2216188 2216188 2216188 TGGTACGGCTCCCTAGGCTGGAACGGGAGCTGAAGCAGCTGCGGGAGGAGAGCGCGCACCTGCGG TGGTACGGCTCCCTAGGCTGGAACGGGAGCTGCAGCAGCTGCGGGAGGAGAGCGCGCACCTGCGG T G MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2213248..2216267 32194978 MeRIP-seq:(Medium) rs1428641288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3971778,Human_RBP_ID_9403100,Human_RBP_ID_19019393,Human_RBP_ID_23080258,Human_RBP_ID_26357515,Human_RBP_ID_27830143 Human_Splice_Rec_837952,Human_Splice_Rec_837953,Human_Splice_Rec_837984,Human_Splice_Rec_837985,Human_Splice_Rec_838020,Human_Splice_Rec_838021,Human_Splice_Rec_838056,Human_Splice_Rec_838057,Human_Splice_Rec_838142,Human_Splice_Rec_838143,Human_Splice_Rec_838156,Human_Splice_Rec_838157,Human_Splice_Rec_838168,Human_Splice_Rec_838169,Human_Splice_Rec_838204,Human_Splice_Rec_838205 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_243306,RMVar_hsa_circ_31714,RMVar_hsa_circ_9871,RMVar_hsa_circ_64796,RMVar_hsa_circ_101973,RMVar_hsa_circ_38270,RMVar_hsa_circ_318575,RMVar_hsa_circ_343244,RMVar_hsa_circ_268090,RMVar_hsa_circ_243307,RMVar_hsa_circ_296354,RMVar_hsa_circ_309050,RMVar_hsa_circ_276152,RMVar_hsa_circ_127460,RMVar_hsa_circ_243309,RMVar_hsa_circ_243310,RMVar_hsa_circ_22640,RMVar_hsa_circ_243311 106084 RMVar_ID_106084 Human_SNP_ID_307313055 m1A Human chr7 - 2219401 2219401 2219401 GATCTCGGAACTGCAGTGGAGCGTGATGGACCAGGAGATGCGGGTGAAGCGCCTGGAGTCGGAGA GATCTCGGAACTGCAGTGGAGCGTGATGGACCTGGAGATGCGGGTGAAGCGCCTGGAGTCGGAGA T A MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:2218026..2220905;chr7:2219319..2219453 26863196 MeRIP-seq:(Medium) rs1246547437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82270,Human_RBP_ID_952339,Human_RBP_ID_3971780,Human_RBP_ID_5622802,Human_RBP_ID_9403103,Human_RBP_ID_18171860,Human_RBP_ID_18472266,Human_RBP_ID_19019396,Human_RBP_ID_22463849,Human_RBP_ID_23080511,Human_RBP_ID_24554910,Human_RBP_ID_26355932,Human_RBP_ID_27829134 Human_Splice_Rec_837948,Human_Splice_Rec_837949,Human_Splice_Rec_837980,Human_Splice_Rec_837981,Human_Splice_Rec_838016,Human_Splice_Rec_838017,Human_Splice_Rec_838052,Human_Splice_Rec_838053,Human_Splice_Rec_838152,Human_Splice_Rec_838153,Human_Splice_Rec_838164,Human_Splice_Rec_838165,Human_Splice_Rec_838176,Human_Splice_Rec_838200,Human_Splice_Rec_838201 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243306,RMVar_hsa_circ_31714,RMVar_hsa_circ_9871,RMVar_hsa_circ_101973,RMVar_hsa_circ_38270,RMVar_hsa_circ_318575,RMVar_hsa_circ_343244,RMVar_hsa_circ_268090,RMVar_hsa_circ_243307,RMVar_hsa_circ_296354,RMVar_hsa_circ_309050,RMVar_hsa_circ_276152,RMVar_hsa_circ_127460,RMVar_hsa_circ_243309,RMVar_hsa_circ_243310,RMVar_hsa_circ_243311,RMVar_hsa_circ_45027,RMVar_hsa_circ_50677,RMVar_hsa_circ_109414,RMVar_hsa_circ_243312,RMVar_hsa_circ_243313 106085 RMVar_ID_106085 Human_SNP_ID_307314183 m1A Human chr7 + 2222646 2222646 2222646 CCTCTTGCTGGCAGCATCCAAGTTCTGCTGACACTGCCTGTTGCGCTCCAGCTGCTCCTGCATCT CCTCTTGCTGGCAGCATCCAAGTTCTGCTGACGCTGCCTGTTGCGCTCCAGCTGCTCCTGCATCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:2222597..2222712;chr7:2222526..2223494 26863196 MeRIP-seq:(Medium) rs765046223 Functional Loss SNV dbSNP153 33..33 33 - - - 106086 RMVar_ID_106086 Human_SNP_ID_307315151 m1A Human chr7 - 2225367 2225367 2225367 GCGGGGCGAGGGTCGGCCCAGACAGCCCCAGGAAGCAAGGGGGCTGTGCACGGTACCTGCCAGGT GCGGGGCGAGGGTCGGCCCAGACAGCCCCAGGGAGCAAGGGGGCTGTGCACGGTACCTGCCAGGT T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2225366..2225499 26863196 MeRIP-seq:(Medium) rs781298469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19134558 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_31714,RMVar_hsa_circ_101973,RMVar_hsa_circ_268090,RMVar_hsa_circ_243307,RMVar_hsa_circ_309050,RMVar_hsa_circ_127460,RMVar_hsa_circ_243311,RMVar_hsa_circ_50677,RMVar_hsa_circ_109414,RMVar_hsa_circ_243312,RMVar_hsa_circ_243313,RMVar_hsa_circ_65957,RMVar_hsa_circ_338959,RMVar_hsa_circ_347772,RMVar_hsa_circ_19803 106087 RMVar_ID_106087 Human_SNP_ID_307317005 m1A Human chr7 - 2230683 2230683 2230683 CTCGCCGGCCTTTGGTCTCCAGGACTTGTCCCAGCAGCCCCTCGAACTGAGAATTACACCATCGG CTCGCCGGCCTTTGGTCTCCAGGACTTGTCCCGGCAGCCCCTCGAACTGAGAATTACACCATCGG T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2230636..2232894 26863196 MeRIP-seq:(Medium) rs780827710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956123,Human_RBP_ID_5480298,Human_RBP_ID_9403109,Human_RBP_ID_18880270,Human_RBP_ID_24206899,Human_RBP_ID_26356173,Human_RBP_ID_27355675 Human_Splice_Rec_838008,Human_Splice_Rec_838044,Human_Splice_Rec_838192 Human_miRNA_ID_2389887,Human_miRNA_ID_2389888,Human_miRNA_ID_2389889,Human_miRNA_ID_2591116,Human_miRNA_ID_2591117,Human_miRNA_ID_2591118 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_31714,RMVar_hsa_circ_101973,RMVar_hsa_circ_243307,RMVar_hsa_circ_127460,RMVar_hsa_circ_243311,RMVar_hsa_circ_50677,RMVar_hsa_circ_109414,RMVar_hsa_circ_243312,RMVar_hsa_circ_243313,RMVar_hsa_circ_338959,RMVar_hsa_circ_347772,RMVar_hsa_circ_243315,RMVar_hsa_circ_284099,RMVar_hsa_circ_284633,RMVar_hsa_circ_299536,RMVar_hsa_circ_243316,RMVar_hsa_circ_108809,RMVar_hsa_circ_243314,RMVar_hsa_circ_243317 106088 RMVar_ID_106088 Human_SNP_ID_307321037 m1A Human chr7 - 2241941 2241941 2241941 TCTCCAGGGGCAGGGCCGGCGGGGCCGTGGGGAGGCCGGGGCCGGCGGCGGAGTCCAGGTGGGGG TCTCCAGGGGCAGGGCCGGCGGGGCCGTGGGGGGGCCGGGGCCGGCGGCGGAGTCCAGGTGGGGG T C AC069288.1,MRM2 Ensembl:ENSG00000286192,Ensembl:ENSG00000122687 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2241922..2242164 26863196 MeRIP-seq:(Medium) rs1056881064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9336980,Human_RBP_ID_19138662 RMVar_hsa_circ_119646,RMVar_hsa_circ_243318 106089 RMVar_ID_106089 Human_SNP_ID_307321267 m1A Human chr7 - 2242258 2242258 2242258 CGACTCCTGGAATCCCCGCGCGCGCTTTTCGTACCTGCACCGCCGCTTCCGGGGGCGTGGCCTCT CGACTCCTGGAATCCCCGCGCGCGCTTTTCGTGCCTGCACCGCCGCTTCCGGGGGCGTGGCCTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2242226..2242800 26863196 MeRIP-seq:(Medium) rs1035032577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_838183,Human_Splice_Rec_838233,Human_Splice_Rec_838245 106090 RMVar_ID_106090 Human_SNP_ID_307321278 m1A Human chr7 + 2242283 2242283 2242283 GTGCAGGTACGAAAAGCGCGCGCGGGGATTCCAGGAGTCGTGGTGACCAGGGAGGGGAGCCGGGC GTGCAGGTACGAAAAGCGCGCGCGGGGATTCCGGGAGTCGTGGTGACCAGGGAGGGGAGCCGGGC A G NUDT1 Ensembl:ENSG00000106268 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr7:2242274..2242468;chr7:2242251..2242434 26863196 MeRIP-seq:(Medium) rs962976346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_838259,Human_Splice_Rec_838267 106091 RMVar_ID_106091 Human_SNP_ID_307321293 m1A Human chr7 + 2242308 2242308 2242308 GGATTCCAGGAGTCGTGGTGACCAGGGAGGGGAGCCGGGCCAGCGGGCGGCAGGAGACTAGGGGA GGATTCCAGGAGTCGTGGTGACCAGGGAGGGGGGCCGGGCCAGCGGGCGGCAGGAGACTAGGGGA A G NUDT1 Ensembl:ENSG00000106268 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:2242226..2242573;chr7:2242226..2242584 26863196 MeRIP-seq:(Medium) rs1458407614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254176 106092 RMVar_ID_106092 Human_SNP_ID_307322058 m1A Human chr7 - 2244690 2244690 2244690 TAGCCCCATCCTCGATGGTCTCTCCTTCTTGCACTTTGCCCCCAAAGCCATTCCACCGGCCGGCC TAGCCCCATCCTCGATGGTCTCTCCTTCTTGCTCTTTGCCCCCAAAGCCATTCCACCGGCCGGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:2244551..2244776;chr7:2244596..2244697;chr7:2244596..2248045 26863196,32194978,32194978 MeRIP-seq:(Medium) rs767068640 Functional Loss SNV dbSNP153 33..33 33 - - - 106093 RMVar_ID_106093 Human_SNP_ID_307322059 m1A Human chr7 - 2244690 2244690 2244690 TAGCCCCATCCTCGATGGTCTCTCCTTCTTGCACTTTGCCCCCAAAGCCATTCCACCGGCCGGCC TAGCCCCATCCTCGATGGTCTCTCCTTCTTGCCCTTTGCCCCCAAAGCCATTCCACCGGCCGGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:2244551..2244776;chr7:2244596..2244697;chr7:2244596..2248045 26863196,32194978,32194978 MeRIP-seq:(Medium) rs767068640 Functional Loss SNV dbSNP153 33..33 33 - - - 106094 RMVar_ID_106094 Human_SNP_ID_307324213 m1A Human chr7 + 2250977 2250977 2250977 TTCCAGGGTCAGGACACCATCCTGGACTACACACTCCGCGAGGTGGACACGGTCTAGCGGGAGCC TTCCAGGGTCAGGACACCATCCTGGACTACACGCTCCGCGAGGTGGACACGGTCTAGCGGGAGCC A G NUDT1 Ensembl:ENSG00000106268 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2250926..2251062 26863196 MeRIP-seq:(Medium) rs766221010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_952344,Human_RBP_ID_1331461,Human_RBP_ID_17665209,Human_RBP_ID_17712789,Human_RBP_ID_18097478,Human_RBP_ID_18211541,Human_RBP_ID_27534894 Human_miRNA_ID_1960354,Human_miRNA_ID_2910008 RMVar_hsa_circ_89537,RMVar_hsa_circ_243319 106095 RMVar_ID_106095 Human_SNP_ID_307324917 m1A Human chr7 - 2252868 2252866 2252869 GTGAGAGAGCAAGGGGGCAGGGGTGAGAGAGCAGGAGAGCAGGGGTGAGGAGAGCAGGAGAGTAG GTGAGAGAGCAAGGGGGCAGGGGTGAGAGAG___GAGAGCAGGGGTGAGGAGAGCAGGAGAGTAG CCTG C SNX8 Ensembl:ENSG00000106266 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2252730..2253162 26863196 MeRIP-seq:(Medium) rs989726693 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_844148 RMVar_hsa_circ_110488,RMVar_hsa_circ_243320 106096 RMVar_ID_106096 Human_SNP_ID_307328837 m1A Human chr7 - 2264300 2264300 2264300 GCGGCAGATCTTCTCATATTCGGGAAGGAGCTAAGGTAGGTGACCTTTCAGCTTCTGCAGGGGCA GCGGCAGATCTTCTCATATTCGGGAAGGAGCTGAGGTAGGTGACCTTTCAGCTTCTGCAGGGGCA T C SNX8 Ensembl:ENSG00000106266 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2257792..2274999 32194978 MeRIP-seq:(Medium) rs1489370810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970746,Human_RBP_ID_19135826 Human_Splice_Rec_838309,Human_Splice_Rec_838327 RMVar_hsa_circ_335837,RMVar_hsa_circ_104580,RMVar_hsa_circ_41853,RMVar_hsa_circ_243322,RMVar_hsa_circ_243321,RMVar_hsa_circ_75366,RMVar_hsa_circ_301551,RMVar_hsa_circ_367150,RMVar_hsa_circ_1604,RMVar_hsa_circ_279619,RMVar_hsa_circ_243325,RMVar_hsa_circ_56076 106097 RMVar_ID_106097 Human_SNP_ID_307333930 m1A Human chr7 - 2278285 2278285 2278285 TCTCCCCTGCAGATCTGCCGACACCCCAGGCCATCGAGCCCCAGGCCATCGTGCAGCAGGTCCCA TCTCCCCTGCAGATCTGCCGACACCCCAGGCCGTCGAGCCCCAGGCCATCGTGCAGCAGGTCCCA T C SNX8 Ensembl:ENSG00000106266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr7:2278155..2278354;chr7:2275098..2299356 26863196,32194978 MeRIP-seq:(Medium) rs967903014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956902,Human_RBP_ID_22463850 Human_Splice_Rec_838300,Human_Splice_Rec_838332,Human_Splice_Rec_838342,Human_Splice_Rec_838352,Human_Splice_Rec_838362,Human_Splice_Rec_838368,Human_Splice_Rec_838372 RMVar_hsa_circ_38791,RMVar_hsa_circ_335837,RMVar_hsa_circ_243321,RMVar_hsa_circ_75366,RMVar_hsa_circ_301551,RMVar_hsa_circ_243326,RMVar_hsa_circ_279619,RMVar_hsa_circ_243325,RMVar_hsa_circ_270434,RMVar_hsa_circ_118340,RMVar_hsa_circ_303700,RMVar_hsa_circ_319645,RMVar_hsa_circ_243327 106098 RMVar_ID_106098 Human_SNP_ID_307344971 m1A Human chr7 - 2312603 2312603 2312603 GAGCAGGGGAGGGATTGTTGCATTTGGTGGGCATCCTCGATGTGAAGACTGTGTCTAGAAAGAAG GAGCAGGGGAGGGATTGTTGCATTTGGTGGGCGTCCTCGATGTGAAGACTGTGTCTAGAAAGAAG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2312602..2312811 26863196 MeRIP-seq:(Medium) rs955179211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 106099 RMVar_ID_106099 Human_SNP_ID_307345559 m1A Human chr7 + 2314129 2314129 2314129 GAGGGCAGGGGACCCCGAGGGACGGAGGCGCGAGAGAGCACGGGGACCCCCAAAGGACAGGCGCG GAGGGCAGGGGACCCCGAGGGACGGAGGCGCGTGAGAGCACGGGGACCCCCAAAGGACAGGCGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:2314125..2314478;chr7:2314127..2314419 26863196 MeRIP-seq:(Medium) rs1346676471 Functional Loss SNV dbSNP153 33..33 33 - - - 106100 RMVar_ID_106100 Human_SNP_ID_307346128 m1A Human chr7 - 2315499 2315497 2315500 AGTGAGTGAGTGGGTGAATGAACGTATGAAGAAGCAGTAAGTGAGTGAGTGAGTGAATGGATGAA AGTGAGTGAGTGGGTGAATGAACGTATGAAG___CAGTAAGTGAGTGAGTGAGTGAATGGATGAA GCTT G SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2315462..2315547 26863196 MeRIP-seq:(Medium) rs1477244218 Functional Loss DEL dbSNP153 32..34 33 - - - 106101 RMVar_ID_106101 Human_SNP_ID_307346355 m1A Human chr7 + 2315991 2315989 2315991 CACTCACTGCTTCTTCATACATTCATTCACCCACACTCACTGCATCCTGCATTCATTCACCCACT CACTCACTGCTTCTTCATACATTCATTCACC__CACTCACTGCATCCTGCATTCATTCACCCACT CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2315605..2316536 26863196 MeRIP-seq:(Medium) rs1276809082 Functional Loss DEL dbSNP153 32..33 33 - - - 106102 RMVar_ID_106102 Human_SNP_ID_307346356 m1A Human chr7 + 2315991 2315991 2315991 CACTCACTGCTTCTTCATACATTCATTCACCCACACTCACTGCATCCTGCATTCATTCACCCACT CACTCACTGCTTCTTCATACATTCATTCACCCTCACTCACTGCATCCTGCATTCATTCACCCACT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2315605..2316536 26863196 MeRIP-seq:(Medium) rs1205976111 Functional Loss SNV dbSNP153 33..33 33 - - - 106103 RMVar_ID_106103 Human_SNP_ID_307346508 m1A Human chr7 - 2316352 2316352 2316352 TGCAGTGCATGAGTGAGTGAGTGAGTGAATGAATGAATGCAGGATGCAGTGAGTGGGTGGGTGAA TGCAGTGCATGAGTGAGTGAGTGAGTGAATGACTGAATGCAGGATGCAGTGAGTGGGTGGGTGAA T G SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2316350..2316589 26863196 MeRIP-seq:(Medium) rs937573291 Functional Loss SNV dbSNP153 33..33 33 - - - 106104 RMVar_ID_106104 Human_SNP_ID_307346628 m1A Human chr7 - 2316641 2316605 2316641 AGTGGGTGAATGAATGAATGCAGGATGCAGTGAGTGAGTGGTTGTGTGAATGAATGCAGGATGCA AGTGGGTGAATGAATGAATGCAGGATGCAGTG_________________________________ GCACTGCATCCTGCATTCATTCACACAACCACTCACT G SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2316633..2316741 26863196 MeRIP-seq:(Medium) rs1414209446 Functional Loss DEL dbSNP153 33..65 33 - - - 106105 RMVar_ID_106105 Human_SNP_ID_307346650 m1A Human chr7 - 2316641 2316641 2316641 AGTGGGTGAATGAATGAATGCAGGATGCAGTGAGTGAGTGGTTGTGTGAATGAATGCAGGATGCA AGTGGGTGAATGAATGAATGCAGGATGCAGTGGGTGAGTGGTTGTGTGAATGAATGCAGGATGCA T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2316633..2316741 26863196 MeRIP-seq:(Medium) rs1486127239 Functional Loss SNV dbSNP153 33..33 33 - - - 106106 RMVar_ID_106106 Human_SNP_ID_307346651 m1A Human chr7 - 2316641 2316641 2316641 AGTGGGTGAATGAATGAATGCAGGATGCAGTGAGTGAGTGGTTGTGTGAATGAATGCAGGATGCA AGTGGGTGAATGAATGAATGCAGGATGCAGTGCGTGAGTGGTTGTGTGAATGAATGCAGGATGCA T G SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2316633..2316741 26863196 MeRIP-seq:(Medium) rs1486127239 Functional Loss SNV dbSNP153 33..33 33 - - - 106107 RMVar_ID_106107 Human_SNP_ID_307359827 m1A Human chr7 - 2354915 2354915 2354915 ACCGCCACGTTCTCCGCGTCCTGCATGGGCCCAACGCTGCCTACTCGCAGGGCTCCGCGGCCGCC ACCGCCACGTTCTCCGCGTCCTGCATGGGCCCGACGCTGCCTACTCGCAGGGCTCCGCGGCCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2354826..2355471 26863196 MeRIP-seq:(Medium) rs1323735327 Functional Loss SNV dbSNP153 33..33 33 - - - 106108 RMVar_ID_106108 Human_SNP_ID_307359874 m1A Human chr7 + 2354983 2354981 2354984 CGAGGCGGCCGAGGAGCGCGCCGAGCCCGGCCAGCAGCAGCCGGCCGCCGAGCCGCCGCCAGCCG CGAGGCGGCCGAGGAGCGCGCCGAGCCCGGC___CAGCAGCCGGCCGCCGAGCCGCCGCCAGCCG CCAG C EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:2354851..2355059 26863196 MeRIP-seq:(Medium) rs1296786409 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_254169,Human_RBP_ID_4956128,Human_RBP_ID_5242940,Human_RBP_ID_8914227,Human_RBP_ID_9263389,Human_RBP_ID_9311147,Human_RBP_ID_9336983,Human_RBP_ID_22463852 106109 RMVar_ID_106109 Human_SNP_ID_307359908 m1A Human chr7 - 2355091 2355064 2355091 TCCTCACCTCGGACTCCGGCCCGGCCTCCGCGATCCCCACCTCCTCACTGGAGGCCTCGGTCCCC TCCTCACCTCGGACTCCGGCCCGGCCTCCGCG___________________________GTCCCC CCGAGGCCTCCAGTGAGGAGGTGGGGAT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:2355076..2355100 26863196 MeRIP-seq:(Medium) rs1178983830 Functional Loss DEL dbSNP153 33..59 33 - - - 106110 RMVar_ID_106110 Human_SNP_ID_307359908 m1A Human chr7 + 2355090 2355064 2355091 CGGGGACCGAGGCCTCCAGTGAGGAGGTGGGGATCGCGGAGGCCGGGCCGGAGTCCGAGGTGAGG CGGGGAC___________________________CGCGGAGGCCGGGCCGGAGTCCGAGGTGAGG CCGAGGCCTCCAGTGAGGAGGTGGGGAT C EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2354826..2360845 26863196 MeRIP-seq:(Medium) rs1178983830 Functional Loss DEL dbSNP153 8..34 33 - - - Human_RBP_ID_86881,Human_RBP_ID_254171,Human_RBP_ID_954105,Human_RBP_ID_3971783,Human_RBP_ID_4935820,Human_RBP_ID_5242941,Human_RBP_ID_7725570,Human_RBP_ID_8910256,Human_RBP_ID_8944147,Human_RBP_ID_9311149,Human_RBP_ID_9336984,Human_RBP_ID_9403110,Human_RBP_ID_21556961,Human_RBP_ID_22463853,Human_RBP_ID_26356178 Human_Splice_Rec_838421 106111 RMVar_ID_106111 Human_SNP_ID_307359915 m1A Human chr7 + 2355082 2355082 2355082 GGAGGCCGCGGGGACCGAGGCCTCCAGTGAGGAGGTGGGGATCGCGGAGGCCGGGCCGGAGTCCG GGAGGCCGCGGGGACCGAGGCCTCCAGTGAGGTGGTGGGGATCGCGGAGGCCGGGCCGGAGTCCG A T EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:2354851..2355150 26863196 MeRIP-seq:(Medium) rs1337514613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86881,Human_RBP_ID_954105,Human_RBP_ID_4956906,Human_RBP_ID_5242941,Human_RBP_ID_7725570,Human_RBP_ID_8914229,Human_RBP_ID_8944147,Human_RBP_ID_9311149,Human_RBP_ID_9336984,Human_RBP_ID_9403110,Human_RBP_ID_18451503,Human_RBP_ID_21556961,Human_RBP_ID_26356178 Human_Splice_Rec_838421 106112 RMVar_ID_106112 Human_SNP_ID_307359925 m1A Human chr7 + 2355090 2355090 2355090 CGGGGACCGAGGCCTCCAGTGAGGAGGTGGGGATCGCGGAGGCCGGGCCGGAGTCCGAGGTGAGG CGGGGACCGAGGCCTCCAGTGAGGAGGTGGGGTTCGCGGAGGCCGGGCCGGAGTCCGAGGTGAGG A T EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2354826..2360845 26863196 MeRIP-seq:(Medium) rs1370667464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86881,Human_RBP_ID_254171,Human_RBP_ID_954105,Human_RBP_ID_3971783,Human_RBP_ID_4935820,Human_RBP_ID_5242941,Human_RBP_ID_7725570,Human_RBP_ID_8910256,Human_RBP_ID_8944147,Human_RBP_ID_9311149,Human_RBP_ID_9336984,Human_RBP_ID_9403110,Human_RBP_ID_21556961,Human_RBP_ID_22463853,Human_RBP_ID_26356178 Human_Splice_Rec_838421 106113 RMVar_ID_106113 Human_SNP_ID_307359926 m1A Human chr7 - 2355091 2355091 2355091 TCCTCACCTCGGACTCCGGCCCGGCCTCCGCGATCCCCACCTCCTCACTGGAGGCCTCGGTCCCC TCCTCACCTCGGACTCCGGCCCGGCCTCCGCGGTCCCCACCTCCTCACTGGAGGCCTCGGTCCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:2355076..2355100 26863196 MeRIP-seq:(Medium) rs1355357340 Functional Loss SNV dbSNP153 33..33 33 - - - 106114 RMVar_ID_106114 Human_SNP_ID_307360122 m1A Human chr7 + 2355337 2355337 2355337 GGGAGGAAACGAGGGCAGAGCGGCCGAGGCCGAACCCCGGGCGCTGGAGAACGGCGACGCGGACG GGGAGGAAACGAGGGCAGAGCGGCCGAGGCCGCACCCCGGGCGCTGGAGAACGGCGACGCGGACG A C EIF3B Ensembl:ENSG00000106263 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:2354876..2355425;chr7:2354119..2360847;chr7:2354185..2360800 26863410,26863196,26863196 MeRIP-seq:(Medium) rs767034532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254173,Human_RBP_ID_4935838,Human_RBP_ID_5479387,Human_RBP_ID_5513073,Human_RBP_ID_8910258,Human_RBP_ID_9263390,Human_RBP_ID_9311153,Human_RBP_ID_9336985,Human_RBP_ID_9404210,Human_RBP_ID_22462977,Human_RBP_ID_26356179 Human_Splice_Rec_838375,Human_Splice_Rec_838387,Human_Splice_Rec_838423,Human_Splice_Rec_838433 106115 RMVar_ID_106115 Human_SNP_ID_307360123 m1A Human chr7 + 2355338 2355338 2355338 GGAGGAAACGAGGGCAGAGCGGCCGAGGCCGAACCCCGGGCGCTGGAGAACGGCGACGCGGACGA GGAGGAAACGAGGGCAGAGCGGCCGAGGCCGATCCCCGGGCGCTGGAGAACGGCGACGCGGACGA A T EIF3B Ensembl:ENSG00000106263 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:2355301..2355375 26863196 MeRIP-seq:(Medium) rs749876972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254173,Human_RBP_ID_4935838,Human_RBP_ID_5479387,Human_RBP_ID_5513073,Human_RBP_ID_8910258,Human_RBP_ID_9263390,Human_RBP_ID_9311153,Human_RBP_ID_9336985,Human_RBP_ID_9404210,Human_RBP_ID_22462977,Human_RBP_ID_26356179 Human_Splice_Rec_838375,Human_Splice_Rec_838387,Human_Splice_Rec_838423,Human_Splice_Rec_838433 106116 RMVar_ID_106116 Human_SNP_ID_307360162 m1A Human chr7 - 2355379 2355376 2355379 TCACGTCGTCCACGAAGTCCTCGGGGTCGCTGAAGGAGGGCTCGTCCGCGTCGCCGTTCTCCAGC TCACGTCGTCCACGAAGTCCTCGGGGTCGCTG___GAGGGCTCGTCCGCGTCGCCGTTCTCCAGC CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2354955..2355425 32194978 MeRIP-seq:(Medium) rs1174591348 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5513076 106117 RMVar_ID_106117 Human_SNP_ID_307360165 m1A Human chr7 - 2355379 2355379 2355379 TCACGTCGTCCACGAAGTCCTCGGGGTCGCTGAAGGAGGGCTCGTCCGCGTCGCCGTTCTCCAGC TCACGTCGTCCACGAAGTCCTCGGGGTCGCTGCAGGAGGGCTCGTCCGCGTCGCCGTTCTCCAGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2354955..2355425 32194978 MeRIP-seq:(Medium) rs1436035971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5513076 106118 RMVar_ID_106118 Human_SNP_ID_307362692 m1A Human chr7 + 2362743 2362743 2362743 CAAGCTTGACAAGCAGCACACATTCCGGGTCAACCTCTTTACGGATTTTGACAAGTGAGTTCAGA CAAGCTTGACAAGCAGCACACATTCCGGGTCAGCCTCTTTACGGATTTTGACAAGTGAGTTCAGA A G EIF3B Ensembl:ENSG00000106263 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2362694..2362806 26863196 MeRIP-seq:(Medium) rs775778858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_681385,Human_RBP_ID_1051517,Human_RBP_ID_2040112,Human_RBP_ID_3971785,Human_RBP_ID_5479398,Human_RBP_ID_5513090,Human_RBP_ID_8146908,Human_RBP_ID_8910271,Human_RBP_ID_9263229,Human_RBP_ID_9310461,Human_RBP_ID_16119013,Human_RBP_ID_17540764,Human_RBP_ID_18097741 Human_Splice_Rec_838378,Human_Splice_Rec_838379,Human_Splice_Rec_838390,Human_Splice_Rec_838391,Human_Splice_Rec_838426,Human_Splice_Rec_838427,Human_Splice_Rec_838436,Human_Splice_Rec_838437 RMVar_hsa_circ_243332,RMVar_hsa_circ_19151,RMVar_hsa_circ_44972,RMVar_hsa_circ_66703,RMVar_hsa_circ_270801,RMVar_hsa_circ_332235,RMVar_hsa_circ_90226,RMVar_hsa_circ_48652,RMVar_hsa_circ_38308,RMVar_hsa_circ_371689,RMVar_hsa_circ_243328,RMVar_hsa_circ_243329,RMVar_hsa_circ_243330,RMVar_hsa_circ_375947,RMVar_hsa_circ_377341,RMVar_hsa_circ_69546,RMVar_hsa_circ_286464,RMVar_hsa_circ_243333,RMVar_hsa_circ_243331 106119 RMVar_ID_106119 Human_SNP_ID_307363302 m1A Human chr7 + 2364433 2364433 2364433 TCCTAAGGGCACCTACCTGGCTACCTTTCATCAAAGAGGCATTGCTCTATGGGGGGGAGAGAAAT TCCTAAGGGCACCTACCTGGCTACCTTTCATCGAAGAGGCATTGCTCTATGGGGGGGAGAGAAAT A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:2363626..2366446 32194978 MeRIP-seq:(Medium) rs764542868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1051522,Human_RBP_ID_2040123,Human_RBP_ID_3081167,Human_RBP_ID_4935872,Human_RBP_ID_5452217,Human_RBP_ID_5479405,Human_RBP_ID_8910282,Human_RBP_ID_9263398,Human_RBP_ID_9311703,Human_RBP_ID_9403114,Human_RBP_ID_18097743,Human_RBP_ID_18451507,Human_RBP_ID_22462978,Human_RBP_ID_22747031,Human_RBP_ID_23081401,Human_RBP_ID_27110897,Human_RBP_ID_27766981 Human_Splice_Rec_838384,Human_Splice_Rec_838385,Human_Splice_Rec_838396,Human_Splice_Rec_838397,Human_Splice_Rec_838432,Human_Splice_Rec_838442,Human_Splice_Rec_838443,Human_Splice_Rec_838470,Human_Splice_Rec_838471,Human_Splice_Rec_838475,Human_Splice_Rec_838477 RMVar_hsa_circ_67893,RMVar_hsa_circ_66703,RMVar_hsa_circ_270801,RMVar_hsa_circ_332235,RMVar_hsa_circ_90226,RMVar_hsa_circ_48652,RMVar_hsa_circ_243328,RMVar_hsa_circ_243329,RMVar_hsa_circ_243330,RMVar_hsa_circ_375947,RMVar_hsa_circ_69546,RMVar_hsa_circ_243333,RMVar_hsa_circ_289465,RMVar_hsa_circ_275651,RMVar_hsa_circ_314130,RMVar_hsa_circ_296863,RMVar_hsa_circ_243334,RMVar_hsa_circ_334441,RMVar_hsa_circ_293031,RMVar_hsa_circ_126752,RMVar_hsa_circ_278018,RMVar_hsa_circ_76094,RMVar_hsa_circ_243335,RMVar_hsa_circ_32145,RMVar_hsa_circ_56018,RMVar_hsa_circ_243337,RMVar_hsa_circ_243338,RMVar_hsa_circ_243339,RMVar_hsa_circ_243336 106120 RMVar_ID_106120 Human_SNP_ID_307363306 m1A Human chr7 + 2364441 2364441 2364441 GCACCTACCTGGCTACCTTTCATCAAAGAGGCATTGCTCTATGGGGGGGAGAGAAATTCAAGCAA GCACCTACCTGGCTACCTTTCATCAAAGAGGCGTTGCTCTATGGGGGGGAGAGAAATTCAAGCAA A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2364359..2364510 32194978 MeRIP-seq:(Medium) rs762029255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_286210,Human_RBP_ID_2040123,Human_RBP_ID_4935872,Human_RBP_ID_5452217,Human_RBP_ID_5479405,Human_RBP_ID_7725595,Human_RBP_ID_8910282,Human_RBP_ID_9263398,Human_RBP_ID_9311160,Human_RBP_ID_9403114,Human_RBP_ID_18108755,Human_RBP_ID_18880547,Human_RBP_ID_22462978,Human_RBP_ID_22834642,Human_RBP_ID_23081401,Human_RBP_ID_26356182,Human_RBP_ID_27110897 Human_Splice_Rec_838384,Human_Splice_Rec_838385,Human_Splice_Rec_838396,Human_Splice_Rec_838397,Human_Splice_Rec_838432,Human_Splice_Rec_838442,Human_Splice_Rec_838443,Human_Splice_Rec_838470,Human_Splice_Rec_838471,Human_Splice_Rec_838475,Human_Splice_Rec_838477 RMVar_hsa_circ_67893,RMVar_hsa_circ_66703,RMVar_hsa_circ_270801,RMVar_hsa_circ_332235,RMVar_hsa_circ_90226,RMVar_hsa_circ_48652,RMVar_hsa_circ_243328,RMVar_hsa_circ_243329,RMVar_hsa_circ_243330,RMVar_hsa_circ_375947,RMVar_hsa_circ_69546,RMVar_hsa_circ_243333,RMVar_hsa_circ_289465,RMVar_hsa_circ_275651,RMVar_hsa_circ_314130,RMVar_hsa_circ_296863,RMVar_hsa_circ_243334,RMVar_hsa_circ_334441,RMVar_hsa_circ_293031,RMVar_hsa_circ_126752,RMVar_hsa_circ_278018,RMVar_hsa_circ_76094,RMVar_hsa_circ_243335,RMVar_hsa_circ_32145,RMVar_hsa_circ_56018,RMVar_hsa_circ_243337,RMVar_hsa_circ_243338,RMVar_hsa_circ_243339,RMVar_hsa_circ_243336 106121 RMVar_ID_106121 Human_SNP_ID_307367452 m1A Human chr7 + 2375446 2375446 2375446 GACACTTCGGACTGCACGGTCATGAACATCGCAGAGCACTACATGGCTTCCGACGTCGAATGGGA GACACTTCGGACTGCACGGTCATGAACATCGCGGAGCACTACATGGCTTCCGACGTCGAATGGGA A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2375342..2375582 26863196 MeRIP-seq:(Medium) rs747712881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83852,Human_RBP_ID_843207,Human_RBP_ID_1685145,Human_RBP_ID_2040156,Human_RBP_ID_3841546,Human_RBP_ID_4935917,Human_RBP_ID_5429425,Human_RBP_ID_5479424,Human_RBP_ID_5513117,Human_RBP_ID_8910309,Human_RBP_ID_9311713,Human_RBP_ID_16119487,Human_RBP_ID_18108292,Human_RBP_ID_18880577,Human_RBP_ID_22834659,Human_RBP_ID_23075250,Human_RBP_ID_27530600 Human_Splice_Rec_838410,Human_Splice_Rec_838411,Human_Splice_Rec_838456,Human_Splice_Rec_838457,Human_Splice_Rec_838487 Human_miRNA_ID_2394912,Human_miRNA_ID_2907052,Human_miRNA_ID_3003651,Human_miRNA_ID_3025886 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_69546,RMVar_hsa_circ_126752,RMVar_hsa_circ_76094,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_243336,RMVar_hsa_circ_119919,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_372337,RMVar_hsa_circ_243346,RMVar_hsa_circ_12308,RMVar_hsa_circ_77706,RMVar_hsa_circ_243347,RMVar_hsa_circ_304285,RMVar_hsa_circ_243348,RMVar_hsa_circ_243349,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351 106122 RMVar_ID_106122 Human_SNP_ID_307367517 m1A Human chr7 - 2375634 2375632 2375634 CTAACACCAGCCAAGGCTTCTGTTCAACACAGAGGCTTGGTGCCCCTTCCCTGAGGTCCCAGGAC CTAACACCAGCCAAGGCTTCTGTTCAACACAG__GCTTGGTGCCCCTTCCCTGAGGTCCCAGGAC CCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2375629..2375721 26863196 MeRIP-seq:(Medium) rs200684025 Functional Loss DEL dbSNP153 33..34 33 - - - 106123 RMVar_ID_106123 Human_SNP_ID_307368632 m1A Human chr7 + 2378249 2378249 2378249 TGACCCTGGGTGTCGAGGAAGGAGAAGGCGCGAGCACTGCTGGGATGCTGTGTTGTGTGAATGAC TGACCCTGGGTGTCGAGGAAGGAGAAGGCGCGGGCACTGCTGGGATGCTGTGTTGTGTGAATGAC A G EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2378237..2378397 26863196 MeRIP-seq:(Medium) rs1290147487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3841549,Human_RBP_ID_8149458,Human_RBP_ID_17166566,Human_RBP_ID_21993701,Human_RBP_ID_24208186 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 106124 RMVar_ID_106124 Human_SNP_ID_307368778 m1A Human chr7 + 2378468 2378452 2378468 GAGCGCTCCTGGGAAGCTGTGTTGTGTGAATGACCCTGGGTGTCATGGAGGAAGGAGCAGGCGCG GAGCGCTCCTGGGAAGC________________CCCTGGGTGTCATGGAGGAAGGAGCAGGCGCG CTGTGTTGTGTGAATGA C EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2378465..2378566 26863196 MeRIP-seq:(Medium) rs1334994384 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_5656949,Human_RBP_ID_17166569,Human_RBP_ID_24208193 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 106125 RMVar_ID_106125 Human_SNP_ID_307368781 m1A Human chr7 + 2378468 2378458 2378468 GAGCGCTCCTGGGAAGCTGTGTTGTGTGAATGACCCTGGGTGTCATGGAGGAAGGAGCAGGCGCG GAGCGCTCCTGGGAAGCTGTGTT__________CCCTGGGTGTCATGGAGGAAGGAGCAGGCGCG TGTGTGAATGA T EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2378465..2378566 26863196 MeRIP-seq:(Medium) rs1223114073 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5656949,Human_RBP_ID_17166569,Human_RBP_ID_24208193 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 106126 RMVar_ID_106126 Human_SNP_ID_307369102 m1A Human chr7 + 2379130 2379130 2379130 TTACCAGTTCTGTGCTTTCCCCAACCTCATGCATAGGAATTGGTGGAGAGAAGGCGCACCATGAT TTACCAGTTCTGTGCTTTCCCCAACCTCATGCGTAGGAATTGGTGGAGAGAAGGCGCACCATGAT A G EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2379126..2379175 32194978 MeRIP-seq:(Medium) rs573885331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83859,Human_RBP_ID_952351,Human_RBP_ID_1685165,Human_RBP_ID_2040166,Human_RBP_ID_4935935,Human_RBP_ID_5429433,Human_RBP_ID_5622841,Human_RBP_ID_22685159,Human_RBP_ID_22746607,Human_RBP_ID_22834666 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 106127 RMVar_ID_106127 Human_SNP_ID_307369103 m1A Human chr7 + 2379130 2379130 2379130 TTACCAGTTCTGTGCTTTCCCCAACCTCATGCATAGGAATTGGTGGAGAGAAGGCGCACCATGAT TTACCAGTTCTGTGCTTTCCCCAACCTCATGCTTAGGAATTGGTGGAGAGAAGGCGCACCATGAT A T EIF3B Ensembl:ENSG00000106263 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2379126..2379175 32194978 MeRIP-seq:(Medium) rs573885331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83859,Human_RBP_ID_952351,Human_RBP_ID_1685165,Human_RBP_ID_2040166,Human_RBP_ID_4935935,Human_RBP_ID_5429433,Human_RBP_ID_5622841,Human_RBP_ID_22685159,Human_RBP_ID_22746607,Human_RBP_ID_22834666 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 106128 RMVar_ID_106128 Human_SNP_ID_307369246 m1A Human chr7 + 2379427 2379427 2379427 GGTGGACACTGACGAGCTGGACAGCAACGTGGACGACTGGGAAGAGGAGACCATTGAGTTCTTCG GGTGGACACTGACGAGCTGGACAGCAACGTGGGCGACTGGGAAGAGGAGACCATTGAGTTCTTCG A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:2379356..2379525 26863410 MeRIP-seq:(Medium) rs1446248317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253188,Human_RBP_ID_793091,Human_RBP_ID_843459,Human_RBP_ID_1685169,Human_RBP_ID_2040168,Human_RBP_ID_3841552,Human_RBP_ID_5122675,Human_RBP_ID_5429441,Human_RBP_ID_5513135,Human_RBP_ID_7725687,Human_RBP_ID_8910320,Human_RBP_ID_9311170,Human_RBP_ID_9403124,Human_RBP_ID_16119568,Human_RBP_ID_27569068 Human_Splice_Rec_838418,Human_Splice_Rec_838419,Human_Splice_Rec_838464,Human_Splice_Rec_838465,Human_Splice_Rec_838492,Human_Splice_Rec_838493,Human_Splice_Rec_838500,Human_Splice_Rec_838501,Human_Splice_Rec_838504,Human_Splice_Rec_838508 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_243350,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_93637,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353,RMVar_hsa_circ_243355 106129 RMVar_ID_106129 Human_SNP_ID_307369334 m1A Human chr7 - 2379598 2379598 2379598 GACACTAGGGCTTCACCCTTCACCCCTGCCTTAAAGGAGGTGCTTCCTCAGTGACGGGGATAACT GACACTAGGGCTTCACCCTTCACCCCTGCCTTCAAGGAGGTGCTTCCTCAGTGACGGGGATAACT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2379594..2379745 32194978 MeRIP-seq:(Medium) rs1024915353 Functional Loss SNV dbSNP153 33..33 33 - - - 106130 RMVar_ID_106130 Human_SNP_ID_307369648 m1A Human chr7 - 2380338 2380338 2380338 GTCACAGTCCAGAGCCAGAGAGCACAGGGAGGAGGCGGGAGTCACGCGGCTTCCTGCAGGACGGC GTCACAGTCCAGAGCCAGAGAGCACAGGGAGGGGGCGGGAGTCACGCGGCTTCCTGCAGGACGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2380144..2380400 32194978 MeRIP-seq:(Medium) rs746281578 Functional Loss SNV dbSNP153 33..33 33 - - - 106131 RMVar_ID_106131 Human_SNP_ID_307369649 m1A Human chr7 - 2380338 2380338 2380338 GTCACAGTCCAGAGCCAGAGAGCACAGGGAGGAGGCGGGAGTCACGCGGCTTCCTGCAGGACGGC GTCACAGTCCAGAGCCAGAGAGCACAGGGAGGCGGCGGGAGTCACGCGGCTTCCTGCAGGACGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2380144..2380400 32194978 MeRIP-seq:(Medium) rs746281578 Functional Loss SNV dbSNP153 33..33 33 - - - 106132 RMVar_ID_106132 Human_SNP_ID_307369653 m1A Human chr7 - 2380350 2380348 2380350 AATCCAGGCGCAGTCACAGTCCAGAGCCAGAGAGCACAGGGAGGAGGCGGGAGTCACGCGGCTTC AATCCAGGCGCAGTCACAGTCCAGAGCCAGAG__CACAGGGAGGAGGCGGGAGTCACGCGGCTTC GCT G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:2380301..2380350;chr7:2380326..2380350 26863196 MeRIP-seq:(Medium) rs1342690099 Functional Loss DEL dbSNP153 33..34 33 - - - 106133 RMVar_ID_106133 Human_SNP_ID_307369669 m1A Human chr7 - 2380371 2380371 2380371 AAAAATGTGTCGCAATGGCAGAATCCAGGCGCAGTCACAGTCCAGAGCCAGAGAGCACAGGGAGG AAAAATGTGTCGCAATGGCAGAATCCAGGCGCTGTCACAGTCCAGAGCCAGAGAGCACAGGGAGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2380178..2380685 26863196 MeRIP-seq:(Medium) rs763651206 Functional Loss SNV dbSNP153 33..33 33 - - - 106134 RMVar_ID_106134 Human_SNP_ID_307369738 m1A Human chr7 + 2380487 2380487 2380487 CACTTCTTTCTTGTTTGGAGTTTTCTGTTGGAACCGCCGGCGTTGGCTCCGAAGACTTAGCGACG CACTTCTTTCTTGTTTGGAGTTTTCTGTTGGACCCGCCGGCGTTGGCTCCGAAGACTTAGCGACG A C EIF3B Ensembl:ENSG00000106263 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2380440..2380541 26863196 MeRIP-seq:(Medium) rs747084056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83866,Human_RBP_ID_681425,Human_RBP_ID_793097,Human_RBP_ID_1051534,Human_RBP_ID_1220895,Human_RBP_ID_1685174,Human_RBP_ID_2040174,Human_RBP_ID_3841555,Human_RBP_ID_5122676,Human_RBP_ID_5153559,Human_RBP_ID_7725689,Human_RBP_ID_8664796,Human_RBP_ID_8910332,Human_RBP_ID_9311175,Human_RBP_ID_16119590,Human_RBP_ID_17665212,Human_RBP_ID_18108293,Human_RBP_ID_18880589,Human_RBP_ID_22110580,Human_RBP_ID_23139961,Human_RBP_ID_23215388,Human_RBP_ID_24515954,Human_RBP_ID_27355898 RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_96549,RMVar_hsa_circ_93637,RMVar_hsa_circ_243354,RMVar_hsa_circ_243355,RMVar_hsa_circ_243356 106135 RMVar_ID_106135 Human_SNP_ID_307369739 m1A Human chr7 + 2380487 2380487 2380487 CACTTCTTTCTTGTTTGGAGTTTTCTGTTGGAACCGCCGGCGTTGGCTCCGAAGACTTAGCGACG CACTTCTTTCTTGTTTGGAGTTTTCTGTTGGATCCGCCGGCGTTGGCTCCGAAGACTTAGCGACG A T EIF3B Ensembl:ENSG00000106263 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2380440..2380541 26863196 MeRIP-seq:(Medium) rs747084056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83866,Human_RBP_ID_681425,Human_RBP_ID_793097,Human_RBP_ID_1051534,Human_RBP_ID_1220895,Human_RBP_ID_1685174,Human_RBP_ID_2040174,Human_RBP_ID_3841555,Human_RBP_ID_5122676,Human_RBP_ID_5153559,Human_RBP_ID_7725689,Human_RBP_ID_8664796,Human_RBP_ID_8910332,Human_RBP_ID_9311175,Human_RBP_ID_16119590,Human_RBP_ID_17665212,Human_RBP_ID_18108293,Human_RBP_ID_18880589,Human_RBP_ID_22110580,Human_RBP_ID_23139961,Human_RBP_ID_23215388,Human_RBP_ID_24515954,Human_RBP_ID_27355898 RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_96549,RMVar_hsa_circ_93637,RMVar_hsa_circ_243354,RMVar_hsa_circ_243355,RMVar_hsa_circ_243356 106136 RMVar_ID_106136 Human_SNP_ID_307369778 m1A Human chr7 - 2380549 2380549 2380549 GCTCGGCTGTGTACAGGCACCGTGGAAACATCACTGGGCGCAGGAGAAGGTGCCGCCAGTGGCGT GCTCGGCTGTGTACAGGCACCGTGGAAACATCCCTGGGCGCAGGAGAAGGTGCCGCCAGTGGCGT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:2380526..2380550 26863196 MeRIP-seq:(Medium) rs1474793280 Functional Loss SNV dbSNP153 33..33 33 - - - 106137 RMVar_ID_106137 Human_SNP_ID_307377764 m1A Human chr7 + 2403644 2403644 2403644 GTCGCGGGGCGGCGGCGGCGGCTGCGGGCGCGAGGTGAGGGGCGCGAGGTGAGGGTCGCGAGGTG GTCGCGGGGCGGCGGCGGCGGCTGCGGGCGCGGGGTGAGGGGCGCGAGGTGAGGGTCGCGAGGTG A G CHST12 Ensembl:ENSG00000136213 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:2403601..2403697;chr7:2403609..2403734 26863196 MeRIP-seq:(Medium) rs1359186513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955580 Human_Splice_Rec_838513,Human_Splice_Rec_838515 106138 RMVar_ID_106138 Human_SNP_ID_307377765 m1A Human chr7 - 2403647 2403647 2403647 CCTCACCTCGCGACCCTCACCTCGCGCCCCTCACCTCGCGCCCGCAGCCGCCGCCGCCGCCCCGC CCTCACCTCGCGACCCTCACCTCGCGCCCCTCTCCTCGCGCCCGCAGCCGCCGCCGCCGCCCCGC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr7:2403634..2403724;chr7:2403611..2403762 26863410,26863196 MeRIP-seq:(Medium) rs1467535940 Functional Loss SNV dbSNP153 33..33 33 - - - 106139 RMVar_ID_106139 Human_SNP_ID_307378314 m1A Human chr7 - 2405493 2405493 2405493 CCCAAACCACCACCAAAGGGATAAAAGTTTAAACTCCCTCACACAGCATTCAGGCCCCTGCACAA CCCAAACCACCACCAAAGGGATAAAAGTTTAAGCTCCCTCACACAGCATTCAGGCCCCTGCACAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2405490..2405757 26863196 MeRIP-seq:(Medium) rs942537880 Functional Loss SNV dbSNP153 33..33 33 - - - 106140 RMVar_ID_106140 Human_SNP_ID_307415267 m1A Human chr7 + 2519832 2519832 2519832 GCTTCGGGTCGGTGCAAGGCAGGCGCACGGGGAAGGGCGCGCCGCGCGGCCGCCACCCCACCATG GCTTCGGGTCGGTGCAAGGCAGGCGCACGGGGGAGGGCGCGCCGCGCGGCCGCCACCCCACCATG A G LFNG Ensembl:ENSG00000106003 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2519806..2519931 26863196 MeRIP-seq:(Medium) rs1021450743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113908,RMVar_hsa_circ_243361 106141 RMVar_ID_106141 Human_SNP_ID_307415372 m1A Human chr7 - 2520143 2520143 2520143 GGGCGCGGGTGGCCGTCGGCGGGGCGGGGGGCAGCCCCGGGCGGCGGGCCCGCATCTCTGCGCGC GGGCGCGGGTGGCCGTCGGCGGGGCGGGGGGCGGCCCCGGGCGGCGGGCCCGCATCTCTGCGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2520098..2520214 26863196 MeRIP-seq:(Medium) rs1180528637 Functional Loss SNV dbSNP153 33..33 33 - - - 106142 RMVar_ID_106142 Human_SNP_ID_307415402 m1A Human chr7 - 2520178 2520178 2520178 TGAAGACGTCTCGGGGCGCGAGCGGCTCGGCCAGGGGGCGCGGGTGGCCGTCGGCGGGGCGGGGG TGAAGACGTCTCGGGGCGCGAGCGGCTCGGCCGGGGGGCGCGGGTGGCCGTCGGCGGGGCGGGGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:2520129..2520261 26863196 MeRIP-seq:(Medium) rs1182456220 Functional Loss SNV dbSNP153 33..33 33 - - - 106143 RMVar_ID_106143 Human_SNP_ID_307422631 m1A Human chr7 + 2539067 2539067 2539067 GGCCTCGGCAGTCACTGCTGCAGGCGCTGCCCACAGCAGCAGCTGCTCCCACGCTGCATGCTGGC GGCCTCGGCAGTCACTGCTGCAGGCGCTGCCCGCAGCAGCAGCTGCTCCCACGCTGCATGCTGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2539024..2539125 32194978 MeRIP-seq:(Medium) rs1302472165 Functional Loss SNV dbSNP153 33..33 33 - - - 106144 RMVar_ID_106144 Human_SNP_ID_307422632 m1A Human chr7 + 2539067 2539067 2539067 GGCCTCGGCAGTCACTGCTGCAGGCGCTGCCCACAGCAGCAGCTGCTCCCACGCTGCATGCTGGC GGCCTCGGCAGTCACTGCTGCAGGCGCTGCCCTCAGCAGCAGCTGCTCCCACGCTGCATGCTGGC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2539024..2539125 32194978 MeRIP-seq:(Medium) rs1302472165 Functional Loss SNV dbSNP153 33..33 33 - - - 106145 RMVar_ID_106145 Human_SNP_ID_307423449 m1A Human chr7 - 2540981 2540981 2540981 TGGAGTGCCTCGAGAGCCCCGGCTCCAGCCCCACGGTACGGTGGTGGGGATAGAGAGCGAGGAGA TGGAGTGCCTCGAGAGCCCCGGCTCCAGCCCCGCGGTACGGTGGTGGGGATAGAGAGCGAGGAGA T C BRAT1 Ensembl:ENSG00000106009 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2540963..2541113 32194978 MeRIP-seq:(Medium) rs1200261080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844034,Human_RBP_ID_19134580 Human_Splice_Rec_838646,Human_Splice_Rec_838647,Human_Splice_Rec_838672,Human_Splice_Rec_838690,Human_Splice_Rec_838697 RMVar_hsa_circ_124148,RMVar_hsa_circ_243368 106146 RMVar_ID_106146 Human_SNP_ID_307424280 m1A Human chr7 - 2542747 2542747 2542747 GATGGCCTGCCAGTGTTCCAGGTGGGCTCACAATAGGGGTGGAAGTGACCTCAGGACCTGCTGCC GATGGCCTGCCAGTGTTCCAGGTGGGCTCACATTAGGGGTGGAAGTGACCTCAGGACCTGCTGCC T A BRAT1 Ensembl:ENSG00000106009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2542745..2542823 26863196 MeRIP-seq:(Medium) rs61673178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23075294,Human_RBP_ID_23259218,Human_RBP_ID_27842833 RMVar_hsa_circ_45891,RMVar_hsa_circ_124148,RMVar_hsa_circ_243368,RMVar_hsa_circ_243369,RMVar_hsa_circ_105410,RMVar_hsa_circ_122173,RMVar_hsa_circ_243370 106147 RMVar_ID_106147 Human_SNP_ID_307424281 m1A Human chr7 - 2542747 2542747 2542747 GATGGCCTGCCAGTGTTCCAGGTGGGCTCACAATAGGGGTGGAAGTGACCTCAGGACCTGCTGCC GATGGCCTGCCAGTGTTCCAGGTGGGCTCACAGTAGGGGTGGAAGTGACCTCAGGACCTGCTGCC T C BRAT1 Ensembl:ENSG00000106009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2542745..2542823 26863196 MeRIP-seq:(Medium) rs61673178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23075294,Human_RBP_ID_23259218,Human_RBP_ID_27842833 RMVar_hsa_circ_45891,RMVar_hsa_circ_124148,RMVar_hsa_circ_243368,RMVar_hsa_circ_243369,RMVar_hsa_circ_105410,RMVar_hsa_circ_122173,RMVar_hsa_circ_243370 106148 RMVar_ID_106148 Human_SNP_ID_307424679 m1A Human chr7 + 2543680 2543680 2543680 CCAGCAGACAGGCCACGCGGGGACTCAGCCGCACCCACAGGGCTTCCGTCCAGGGGCTCTGGCAG CCAGCAGACAGGCCACGCGGGGACTCAGCCGCGCCCACAGGGCTTCCGTCCAGGGGCTCTGGCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2543192..2543992 32194978 MeRIP-seq:(Medium) rs773293971 Functional Loss SNV dbSNP153 33..33 33 - - - 106149 RMVar_ID_106149 Human_SNP_ID_307428868 m1A Human chr7 - 2555072 2555072 2555072 TCTCCCCCCCGCCGGCTTCAGATGCAGCCACCACTAATCCTGGGAGGGACAGACACACGGACAGG TCTCCCCCCCGCCGGCTTCAGATGCAGCCACCGCTAATCCTGGGAGGGACAGACACACGGACAGG T C BRAT1 Ensembl:ENSG00000106009 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2555070..2555480 26863196 MeRIP-seq:(Medium) rs1428678752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122173,RMVar_hsa_circ_243370 106150 RMVar_ID_106150 Human_SNP_ID_307428884 m1A Human chr7 + 2555102 2555102 2555102 AGTGGTGGCTGCATCTGAAGCCGGCGGGGGGGAGAGGGGGGCGGCGGGGTGCGGAAAGGAAGGGG AGTGGTGGCTGCATCTGAAGCCGGCGGGGGGGGGAGGGGGGCGGCGGGGTGCGGAAAGGAAGGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2555099..2555490 26863196 MeRIP-seq:(Medium) rs1384786338 Functional Loss SNV dbSNP153 33..33 33 - - - 106151 RMVar_ID_106151 Human_SNP_ID_307429133 m1A Human chr7 + 2555670 2555670 2555670 GGGCCCAGACTTGAAGGAAGGAGTTCAAGCTGAGAGGGGCTGGGGACAGGCAGGCGCCAAGCCGG GGGCCCAGACTTGAAGGAAGGAGTTCAAGCTGGGAGGGGCTGGGGACAGGCAGGCGCCAAGCCGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2555619..2555702 26863196 MeRIP-seq:(Medium) rs1350338343 Functional Loss SNV dbSNP153 33..33 33 - - - 106152 RMVar_ID_106152 Human_SNP_ID_307430367 m1A Human chr7 + 2559107 2559107 2559107 CGCCAGGGAAGGCCCCGAGGCTGCGGGCGGCCAGGGCTGCCCGCGGATTCCCAGACCCGGACGCC CGCCAGGGAAGGCCCCGAGGCTGCGGGCGGCCCGGGCTGCCCGCGGATTCCCAGACCCGGACGCC A C IQCE Ensembl:ENSG00000106012 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2559057..2559367 26863196 MeRIP-seq:(Medium) rs554076788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90369,RMVar_hsa_circ_243373 106153 RMVar_ID_106153 Human_SNP_ID_307430368 m1A Human chr7 + 2559107 2559107 2559107 CGCCAGGGAAGGCCCCGAGGCTGCGGGCGGCCAGGGCTGCCCGCGGATTCCCAGACCCGGACGCC CGCCAGGGAAGGCCCCGAGGCTGCGGGCGGCCGGGGCTGCCCGCGGATTCCCAGACCCGGACGCC A G IQCE Ensembl:ENSG00000106012 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2559057..2559367 26863196 MeRIP-seq:(Medium) rs554076788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90369,RMVar_hsa_circ_243373 106154 RMVar_ID_106154 Human_SNP_ID_307430850 m1A Human chr7 - 2560247 2560247 2560247 GCCCGCGTCCCAACGGGCTTTCTTTTTTTTTGAGACAGGGCCTCACTCTGTTGCCCAGGCTGGAG GCCCGCGTCCCAACGGGCTTTCTTTTTTTTTGGGACAGGGCCTCACTCTGTTGCCCAGGCTGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2560242..2560315 26863196 MeRIP-seq:(Medium) rs1418852313 Functional Loss SNV dbSNP153 33..33 33 - - - 106155 RMVar_ID_106155 Human_SNP_ID_307440327 m1A Human chr7 + 2586606 2586606 2586606 ACATCCCTGGAGGAGACAATGCTGTGGGAGGGAGAGAGGAGCTGGGTCAGATGCGTGACATGTGT ACATCCCTGGAGGAGACAATGCTGTGGGAGGGGGAGAGGAGCTGGGTCAGATGCGTGACATGTGT A G IQCE Ensembl:ENSG00000106012 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2586603..2586911 26863196 MeRIP-seq:(Medium) rs552465001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66428,RMVar_hsa_circ_49184,RMVar_hsa_circ_46140 106156 RMVar_ID_106156 Human_SNP_ID_307441529 m1A Human chr7 + 2590025 2590025 2590025 GCTGCACAGACAGCCACGAGGGGACCGCAACAAGGACCACGAGCGTCTCCGAGGGGCTGTGAGAG GCTGCACAGACAGCCACGAGGGGACCGCAACAGGGACCACGAGCGTCTCCGAGGGGCTGTGAGAG A G IQCE Ensembl:ENSG00000106012 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2589976..2590149 26863196 MeRIP-seq:(Medium) rs1165692420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_838735,Human_Splice_Rec_838777,Human_Splice_Rec_838833,Human_Splice_Rec_838865,Human_Splice_Rec_838903,Human_Splice_Rec_838945,Human_Splice_Rec_838981,Human_Splice_Rec_839021,Human_Splice_Rec_839057,Human_Splice_Rec_839109 RMVar_hsa_circ_66428,RMVar_hsa_circ_49184,RMVar_hsa_circ_46140,RMVar_hsa_circ_243379,RMVar_hsa_circ_113048,RMVar_hsa_circ_335455 106157 RMVar_ID_106157 Human_SNP_ID_307442618 m1A Human chr7 + 2593087 2593087 2593087 CGACCTGGAGAAGGAGCTGGAGTGCGCGAGGGAGGGCGAGGAGGAGAGGAGAGAGCGAGAGGAGG CGACCTGGAGAAGGAGCTGGAGTGCGCGAGGGGGGGCGAGGAGGAGAGGAGAGAGCGAGAGGAGG A G IQCE Ensembl:ENSG00000106012 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2593036..2593179 26863196 MeRIP-seq:(Medium) rs1284734493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_838736,Human_Splice_Rec_838737,Human_Splice_Rec_838778,Human_Splice_Rec_838779,Human_Splice_Rec_838834,Human_Splice_Rec_838835,Human_Splice_Rec_838866,Human_Splice_Rec_838867,Human_Splice_Rec_838904,Human_Splice_Rec_838905,Human_Splice_Rec_838946,Human_Splice_Rec_838947,Human_Splice_Rec_838982,Human_Splice_Rec_838983,Human_Splice_Rec_839022,Human_Splice_Rec_839023,Human_Splice_Rec_839058,Human_Splice_Rec_839059,Human_Splice_Rec_839110,Human_Splice_Rec_839111 RMVar_hsa_circ_66428,RMVar_hsa_circ_46140,RMVar_hsa_circ_243379,RMVar_hsa_circ_113048 106158 RMVar_ID_106158 Human_SNP_ID_307442633 m1A Human chr7 + 2593114 2593112 2593115 GAGGGAGGGCGAGGAGGAGAGGAGAGAGCGAGAGGAGGTTTTGAGGTATGTGACCCGGGTCAGGG GAGGGAGGGCGAGGAGGAGAGGAGAGAGCGA___GAGGTTTTGAGGTATGTGACCCGGGTCAGGG AGAG A IQCE Ensembl:ENSG00000106012 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:2589959..2594976;chr7:2589999..2594976;chr7:2593034..2593181 26863196 MeRIP-seq:(Medium) rs923640473 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_19135859 Human_Splice_Rec_838736,Human_Splice_Rec_838737,Human_Splice_Rec_838778,Human_Splice_Rec_838779,Human_Splice_Rec_838834,Human_Splice_Rec_838835,Human_Splice_Rec_838866,Human_Splice_Rec_838867,Human_Splice_Rec_838904,Human_Splice_Rec_838905,Human_Splice_Rec_838946,Human_Splice_Rec_838947,Human_Splice_Rec_838982,Human_Splice_Rec_838983,Human_Splice_Rec_839022,Human_Splice_Rec_839023,Human_Splice_Rec_839058,Human_Splice_Rec_839059,Human_Splice_Rec_839110,Human_Splice_Rec_839111 RMVar_hsa_circ_66428,RMVar_hsa_circ_46140,RMVar_hsa_circ_243379,RMVar_hsa_circ_113048 106159 RMVar_ID_106159 Human_SNP_ID_307443273 m1A Human chr7 + 2594840 2594840 2594840 CCGCCCCACCCTGCCCTGTGCCGGCCTTCATCACATAGTGACAGGTGAGGTGTCTCATCTTTTCC CCGCCCCACCCTGCCCTGTGCCGGCCTTCATCCCATAGTGACAGGTGAGGTGTCTCATCTTTTCC A C IQCE Ensembl:ENSG00000106012 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2594837..2594910 26863196 MeRIP-seq:(Medium) rs1386295580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66428,RMVar_hsa_circ_46140,RMVar_hsa_circ_243379,RMVar_hsa_circ_113048,RMVar_hsa_circ_243380 106160 RMVar_ID_106160 Human_SNP_ID_307449454 m1A Human chr7 - 2612707 2612707 2612707 CTAGGCCCCGCCCACAGCTCACCTCTCCCGTGACTAGGCCCCGCCCACAGCTCACCTTTCCCATG CTAGGCCCCGCCCACAGCTCACCTCTCCCGTGGCTAGGCCCCGCCCACAGCTCACCTTTCCCATG T C lnc-BRAT1-2,lnc-BRAT1-2:2 RNACentral:URS00008B7D3D,RNACentral:URS00008B91B7 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2612463..2612954 26863196 MeRIP-seq:(Medium) rs912893152 Functional Loss SNV dbSNP153 33..33 33 - - - 106161 RMVar_ID_106161 Human_SNP_ID_307449466 m1A Human chr7 - 2612719 2612719 2612719 CCCCTCCCATGACTAGGCCCCGCCCACAGCTCACCTCTCCCGTGACTAGGCCCCGCCCACAGCTC CCCCTCCCATGACTAGGCCCCGCCCACAGCTCGCCTCTCCCGTGACTAGGCCCCGCCCACAGCTC T C lnc-BRAT1-2,lnc-BRAT1-2:2 RNACentral:URS00008B7D3D,RNACentral:URS00008B91B7 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2612455..2612986 26863196 MeRIP-seq:(Medium) rs1379708562 Functional Loss SNV dbSNP153 33..33 33 - - - 106162 RMVar_ID_106162 Human_SNP_ID_307455866 m1A Human chr7 - 2632071 2632071 2632071 TGGCCCGGGGCGCGGGCTTCAGGGACCCGTCGACCCCCGCCTGGCCGCCCGCATCATCCGCGCGC TGGCCCGGGGCGCGGGCTTCAGGGACCCGTCGTCCCCCGCCTGGCCGCCCGCATCATCCGCGCGC T A - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:2631971..2632099 26863410 MeRIP-seq:(Medium) rs1003247035 Functional Loss SNV dbSNP153 33..33 33 - - - 106163 RMVar_ID_106163 Human_SNP_ID_307455867 m1A Human chr7 - 2632071 2632071 2632071 TGGCCCGGGGCGCGGGCTTCAGGGACCCGTCGACCCCCGCCTGGCCGCCCGCATCATCCGCGCGC TGGCCCGGGGCGCGGGCTTCAGGGACCCGTCGCCCCCCGCCTGGCCGCCCGCATCATCCGCGCGC T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:2631971..2632099 26863410 MeRIP-seq:(Medium) rs1003247035 Functional Loss SNV dbSNP153 33..33 33 - - - 106164 RMVar_ID_106164 Human_SNP_ID_307455878 m1A Human chr7 + 2632111 2632111 2632111 TCCCTGAAGCCCGCGCCCCGGGCCAGCAAGGGAGCCCCGCGCAGGCCGCGCGCATCCGGAGGCGG TCCCTGAAGCCCGCGCCCCGGGCCAGCAAGGGGGCCCCGCGCAGGCCGCGCGCATCCGGAGGCGG A G TTYH3 Ensembl:ENSG00000136295 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:2631926..2645553;chr7:2632076..2632230 26863196 MeRIP-seq:(Medium) rs866709381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955589,Human_RBP_ID_22463407 106165 RMVar_ID_106165 Human_SNP_ID_307460613 m1A Human chr7 - 2646811 2646810 2646811 GGCAGGAAGCGGCGCTGGAGGGGTGGACCCCCAGCTCAGAGTCCCACGCCCCGCCCCAGCAGGGG GGCAGGAAGCGGCGCTGGAGGGGTGGACCCCC_GCTCAGAGTCCCACGCCCCGCCCCAGCAGGGG CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2646810..2646955 26863196 MeRIP-seq:(Medium) rs781681888 Functional Loss DEL dbSNP153 33..33 33 - - - 106166 RMVar_ID_106166 Human_SNP_ID_307461542 m1A Human chr7 - 2648766 2648766 2648766 CTCAGGTCTCCTTGGGCACAGCGTGAAGCTGCACCCCCCCCCACCACCCTACTGCAGGCCTTCAC CTCAGGTCTCCTTGGGCACAGCGTGAAGCTGCCCCCCCCCCCACCACCCTACTGCAGGCCTTCAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2648762..2648880 26863196 MeRIP-seq:(Medium) rs1198996811 Functional Loss SNV dbSNP153 33..33 33 - - - 106167 RMVar_ID_106167 Human_SNP_ID_307461668 m1A Human chr7 + 2649003 2649001 2649003 GTGTGGGGCCTGCACTGGGGTGTGTTTTGGGGATCTGAACTGGGATATGGGGGACTCGTGGTGGG GTGTGGGGCCTGCACTGGGGTGTGTTTTGGG__TCTGAACTGGGATATGGGGGACTCGTGGTGGG GGA G TTYH3 Ensembl:ENSG00000136295 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2648977..2649129 26863196 MeRIP-seq:(Medium) rs1159112278 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3970760,Human_RBP_ID_5403715,Human_RBP_ID_8150365,Human_RBP_ID_8218186,Human_RBP_ID_9439194,Human_RBP_ID_18466481 RMVar_hsa_circ_85335,RMVar_hsa_circ_49497,RMVar_hsa_circ_327910,RMVar_hsa_circ_348690,RMVar_hsa_circ_306521,RMVar_hsa_circ_243383 106168 RMVar_ID_106168 Human_SNP_ID_307461670 m1A Human chr7 + 2649003 2649003 2649003 GTGTGGGGCCTGCACTGGGGTGTGTTTTGGGGATCTGAACTGGGATATGGGGGACTCGTGGTGGG GTGTGGGGCCTGCACTGGGGTGTGTTTTGGGGCTCTGAACTGGGATATGGGGGACTCGTGGTGGG A C TTYH3 Ensembl:ENSG00000136295 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2648977..2649129 26863196 MeRIP-seq:(Medium) rs1365047130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970760,Human_RBP_ID_5403715,Human_RBP_ID_8150365,Human_RBP_ID_8218186,Human_RBP_ID_9439194,Human_RBP_ID_18466481 RMVar_hsa_circ_85335,RMVar_hsa_circ_49497,RMVar_hsa_circ_327910,RMVar_hsa_circ_348690,RMVar_hsa_circ_306521,RMVar_hsa_circ_243383 106169 RMVar_ID_106169 Human_SNP_ID_307461671 m1A Human chr7 + 2649003 2649003 2649003 GTGTGGGGCCTGCACTGGGGTGTGTTTTGGGGATCTGAACTGGGATATGGGGGACTCGTGGTGGG GTGTGGGGCCTGCACTGGGGTGTGTTTTGGGGGTCTGAACTGGGATATGGGGGACTCGTGGTGGG A G TTYH3 Ensembl:ENSG00000136295 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2648977..2649129 26863196 MeRIP-seq:(Medium) rs1365047130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3970760,Human_RBP_ID_5403715,Human_RBP_ID_8150365,Human_RBP_ID_8218186,Human_RBP_ID_9439194,Human_RBP_ID_18466481 RMVar_hsa_circ_85335,RMVar_hsa_circ_49497,RMVar_hsa_circ_327910,RMVar_hsa_circ_348690,RMVar_hsa_circ_306521,RMVar_hsa_circ_243383 106170 RMVar_ID_106170 Human_SNP_ID_307462297 m1A Human chr7 + 2650758 2650758 2650758 GGAGGGAGGGAGGCAGGGGAGAGATTTGACCCATGATTGAAGGTCCCTTTCAAAGCTTCCTCAGG GGAGGGAGGGAGGCAGGGGAGAGATTTGACCCGTGATTGAAGGTCCCTTTCAAAGCTTCCTCAGG A G TTYH3 Ensembl:ENSG00000136295 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2650756..2651026 26863196 MeRIP-seq:(Medium) rs141627044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3083544,Human_RBP_ID_22834894 RMVar_hsa_circ_22287,RMVar_hsa_circ_49497,RMVar_hsa_circ_348690,RMVar_hsa_circ_306521,RMVar_hsa_circ_101339,RMVar_hsa_circ_23258,RMVar_hsa_circ_243384 106171 RMVar_ID_106171 Human_SNP_ID_307463035 m1A Human chr7 + 2652877 2652877 2652877 TTGGAGGGTCCTGGGGAGGGAGAGGCGGGCGGACCCAGCAGCGCCCATGGACTTGGTCTCCTCTC TTGGAGGGTCCTGGGGAGGGAGAGGCGGGCGGGCCCAGCAGCGCCCATGGACTTGGTCTCCTCTC A G TTYH3 Ensembl:ENSG00000136295 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2652871..2652946 26863196 MeRIP-seq:(Medium) rs1466738986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5402816,Human_RBP_ID_8218192,Human_RBP_ID_22366529,Human_RBP_ID_22554567,Human_RBP_ID_24389375 RMVar_hsa_circ_22287,RMVar_hsa_circ_49497,RMVar_hsa_circ_348690,RMVar_hsa_circ_306521,RMVar_hsa_circ_101339,RMVar_hsa_circ_23258,RMVar_hsa_circ_243384,RMVar_hsa_circ_243385,RMVar_hsa_circ_319486 106172 RMVar_ID_106172 Human_SNP_ID_307464513 m1A Human chr7 - 2657408 2657403 2657409 TCACCATCACCATCACCATCACCACCACCACAACCACCACCACCATCATCACCATCATCACCATC TCACCATCACCATCACCATCACCACCACCAC______CACCACCATCATCACCATCATCACCATC GGTGGTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2657406..2657487 26863196 MeRIP-seq:(Medium) rs1320908050 Functional Loss DEL dbSNP153 32..37 33 - - - 106173 RMVar_ID_106173 Human_SNP_ID_307465002 m1A Human chr7 + 2658960 2658960 2658960 CTCATGCCTCAGGAGCCAGAACGCTAATTTCCAGAACCCCCGCTGTGAGAACACCCCACTCATTG CTCATGCCTCAGGAGCCAGAACGCTAATTTCCGGAACCCCCGCTGTGAGAACACCCCACTCATTG A G TTYH3 Ensembl:ENSG00000136295 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2658342..2659045 26863196 MeRIP-seq:(Medium) rs1319693210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682024,Human_RBP_ID_4936799,Human_RBP_ID_17315983 Human_Splice_Rec_839158,Human_Splice_Rec_839159,Human_Splice_Rec_839182,Human_Splice_Rec_839183,Human_Splice_Rec_839204,Human_Splice_Rec_839205,Human_Splice_Rec_839222,Human_Splice_Rec_839223 RMVar_hsa_circ_22287,RMVar_hsa_circ_49497,RMVar_hsa_circ_96087,RMVar_hsa_circ_243386 106174 RMVar_ID_106174 Human_SNP_ID_307466070 m1A Human chr7 + 2662006 2662006 2662006 CCCCAGCCCTGCACGCCACCCACTATCCCGGCACGCTCCCTCTGCAGATGGTCGCCGCACCTACA CCCCAGCCCTGCACGCCACCCACTATCCCGGCGCGCTCCCTCTGCAGATGGTCGCCGCACCTACA A G TTYH3 Ensembl:ENSG00000136295 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:2661651..2662075 26863410 MeRIP-seq:(Medium) rs1341744301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_682032,Human_RBP_ID_794278,Human_RBP_ID_7728092,Human_RBP_ID_17315547,Human_RBP_ID_18098220,Human_RBP_ID_18959053,Human_RBP_ID_26546017,Human_RBP_ID_27530800 106175 RMVar_ID_106175 Human_SNP_ID_307466677 m1A Human chr7 - 2663946 2663946 2663946 TGGAGTAGTTAGGAACACGGCACCGAAAACTCAGAACAAAAATACAACCAATGGCAGGCGCTCCC TGGAGTAGTTAGGAACACGGCACCGAAAACTCTGAACAAAAATACAACCAATGGCAGGCGCTCCC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:2663901..2663975 26863196 MeRIP-seq:(Medium) rs1403344272 Functional Loss SNV dbSNP153 33..33 33 - - - 106176 RMVar_ID_106176 Human_SNP_ID_307466678 m1A Human chr7 - 2663946 2663946 2663946 TGGAGTAGTTAGGAACACGGCACCGAAAACTCAGAACAAAAATACAACCAATGGCAGGCGCTCCC TGGAGTAGTTAGGAACACGGCACCGAAAACTCGGAACAAAAATACAACCAATGGCAGGCGCTCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:2663901..2663975 26863196 MeRIP-seq:(Medium) rs1403344272 Functional Loss SNV dbSNP153 33..33 33 - - - 106177 RMVar_ID_106177 Human_SNP_ID_307529775 m1A Human chr7 - 2844280 2844257 2844280 GGGCCTCGGAGCGACTGCAGCGGCGGCGGCGGACGCGGCCTGAGGCGAGCGGCGGGGCGTGGGGC GGGCCTCGGAGCGACTGCAGCGGCGGCGGCGG_______________________GGCGTGGGGC CCCGCCGCTCGCCTCAGGCCGCGT C GNA12 Ensembl:ENSG00000146535 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr7:2844029..2844325;chr7:2843948..2844325;chr7:2843899..2844350 26863196 MeRIP-seq:(Medium) rs1284389952 Functional Loss DEL dbSNP153 33..55 33 - - - Human_RBP_ID_4955617,Human_RBP_ID_22463862 106178 RMVar_ID_106178 Human_SNP_ID_307529791 m1A Human chr7 - 2844280 2844280 2844280 GGGCCTCGGAGCGACTGCAGCGGCGGCGGCGGACGCGGCCTGAGGCGAGCGGCGGGGCGTGGGGC GGGCCTCGGAGCGACTGCAGCGGCGGCGGCGGGCGCGGCCTGAGGCGAGCGGCGGGGCGTGGGGC T C GNA12 Ensembl:ENSG00000146535 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr7:2844029..2844325;chr7:2843948..2844325;chr7:2843899..2844350 26863196 MeRIP-seq:(Medium) rs1288068142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955617,Human_RBP_ID_22463862 106179 RMVar_ID_106179 Human_SNP_ID_307562704 m1A Human chr7 + 2944471 2944471 2944471 GCAGCTCGCAGCGTTGCAGGTCCTTGGCCTTCATCTGCTGCTGCAGCTTGATGACCTCGTTCATC GCAGCTCGCAGCGTTGCAGGTCCTTGGCCTTCGTCTGCTGCTGCAGCTTGATGACCTCGTTCATC A G CARD11-AS1 Ensembl:ENSG00000237286 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2944421..2946607 32194978 MeRIP-seq:(Medium) rs1490689453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_839377 106180 RMVar_ID_106180 Human_SNP_ID_308156682 m1A Human chr7 - 4642325 4642325 4642325 AATCCAGCTTCCACCCGTCACTCGCGCACCCGACATTGGGCAGGCGACCCCACCGCCCCGGAACA AATCCAGCTTCCACCCGTCACTCGCGCACCCGTCATTGGGCAGGCGACCCCACCGCCCCGGAACA T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:4642278..4642399 26863196 MeRIP-seq:(Medium) rs1377001908 Functional Loss SNV dbSNP153 33..33 33 - - - 106181 RMVar_ID_106181 Human_SNP_ID_308168575 m1A Human chr7 + 4682372 4682372 4682372 GCGCCCTGCTCGCGCTGCGCTCGGCGCCCTGCAGCCCAGTGCTGTGCGCCGCAGCCGCCGCCGCC GCGCCCTGCTCGCGCTGCGCTCGGCGCCCTGCCGCCCAGTGCTGTGCGCCGCAGCCGCCGCCGCC A C FOXK1 Ensembl:ENSG00000164916 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:4682301..4682425 26863410 MeRIP-seq:(Medium) rs1485456276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956138 Human_miRNA_ID_1159719,Human_miRNA_ID_2553317 RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 106182 RMVar_ID_106182 Human_SNP_ID_308168906 m1A Human chr7 - 4683130 4683130 4683130 CCCAGAGTCCAGGCCGGTGGGGGTCGGGGGCGACGGGGTATCCAGACCGGGGAAAGTGGAGGAGA CCCAGAGTCCAGGCCGGTGGGGGTCGGGGGCGCCGGGGTATCCAGACCGGGGAAAGTGGAGGAGA T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:4683049..4683275 26863196 MeRIP-seq:(Medium) rs1464185784 Functional Loss SNV dbSNP153 33..33 33 - - - 106183 RMVar_ID_106183 Human_SNP_ID_308171185 m1A Human chr7 - 4690007 4690007 4690007 GCAGGCTGATCCTTCACGTGGAGAAGCGAGACAGCACCACCTGAGTTTTCACGTCTACTCGCTGG GCAGGCTGATCCTTCACGTGGAGAAGCGAGACGGCACCACCTGAGTTTTCACGTCTACTCGCTGG T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4690004..4690157 26863196 MeRIP-seq:(Medium) rs1364294425 Functional Loss SNV dbSNP153 33..33 33 - - - 106184 RMVar_ID_106184 Human_SNP_ID_308171214 m1A Human chr7 + 4690071 4690071 4690071 CAGTGCCAAAGGCGAAGGGAAGAGCTGTGATTAGGGAGGGTTGGTCTGTTAGTGAAGGAAGCCAC CAGTGCCAAAGGCGAAGGGAAGAGCTGTGATTTGGGAGGGTTGGTCTGTTAGTGAAGGAAGCCAC A T FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:4690069..4690232 26863196 MeRIP-seq:(Medium) rs1254661477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843435,Human_RBP_ID_3090869,Human_RBP_ID_16168263 RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 106185 RMVar_ID_106185 Human_SNP_ID_308179892 m1A Human chr7 - 4716945 4716945 4716945 CCAGCCACACGCCTCCCAGCCATGCGCCTCCCACCACGTACAACTTGCCCTTCACCTGGGGATGT CCAGCCACACGCCTCCCAGCCATGCGCCTCCCCCCACGTACAACTTGCCCTTCACCTGGGGATGT T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:4716943..4717377 26863196 MeRIP-seq:(Medium) rs539043026 Functional Loss SNV dbSNP153 33..33 33 - - - 106186 RMVar_ID_106186 Human_SNP_ID_308179966 m1A Human chr7 + 4717103 4717103 4717103 GCTGGAATGTGGTGGCGGGAGGCACGTGGTTGAGAGGTGCGTGGCTGGGAAGGCATATGGCTGGA GCTGGAATGTGGTGGCGGGAGGCACGTGGTTGGGAGGTGCGTGGCTGGGAAGGCATATGGCTGGA A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:4716905..4717615 26863196 MeRIP-seq:(Medium) rs1314385467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843443,Human_RBP_ID_3860401,Human_RBP_ID_5153152,Human_RBP_ID_5221207,Human_RBP_ID_5327770,Human_RBP_ID_5656966,Human_RBP_ID_8150383,Human_RBP_ID_8218198,Human_RBP_ID_8237675,Human_RBP_ID_8944243,Human_RBP_ID_21992287,Human_RBP_ID_22483268,Human_RBP_ID_26794286 RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 106187 RMVar_ID_106187 Human_SNP_ID_308180010 m1A Human chr7 - 4717225 4717225 4717225 CACCACCTTCCAGCCACATGCCTCTCGCCACCACCTTCCAGCCACATGCCTCCCAGCCACACACC CACCACCTTCCAGCCACATGCCTCTCGCCACCGCCTTCCAGCCACATGCCTCCCAGCCACACACC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4716910..4717614 26863196 MeRIP-seq:(Medium) rs1447330011 Functional Loss SNV dbSNP153 33..33 33 - - - 106188 RMVar_ID_106188 Human_SNP_ID_308180023 m1A Human chr7 + 4717249 4717249 4717249 CTGGAAGGTGGTGGCGAGAGGCATGTGGCTGGAAGGTGGTGGCGGGAGGCATATGGCTGGAAGGT CTGGAAGGTGGTGGCGAGAGGCATGTGGCTGGGAGGTGGTGGCGGGAGGCATATGGCTGGAAGGT A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:4716923..4717574 26863196 MeRIP-seq:(Medium) rs1207276506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860402,Human_RBP_ID_5327771,Human_RBP_ID_5656967,Human_RBP_ID_8218199,Human_RBP_ID_17315991,Human_RBP_ID_18959078,Human_RBP_ID_21992288,Human_RBP_ID_22483269 RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 106189 RMVar_ID_106189 Human_SNP_ID_308187681 m1A Human chr7 + 4740897 4740897 4740897 CATCAAGATCCAGTTCACGTCGCTCTATCACAAAGAAGAGGCCCCAGCCTCCCCGCTGCGGCCAC CATCAAGATCCAGTTCACGTCGCTCTATCACAGAGAAGAGGCCCCAGCCTCCCCGCTGCGGCCAC A G FOXK1 Ensembl:ENSG00000164916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:4740807..4741000 26863196 MeRIP-seq:(Medium) rs762227813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9404232,Human_RBP_ID_17314402,Human_RBP_ID_17426837 Human_Splice_Rec_839726 Human_miRNA_ID_1360652,Human_miRNA_ID_1397671,Human_miRNA_ID_2683807,Human_miRNA_ID_2713538,Human_miRNA_ID_3049514 RMVar_hsa_circ_122648,RMVar_hsa_circ_243447,RMVar_hsa_circ_365207,RMVar_hsa_circ_243446,RMVar_hsa_circ_270863 106190 RMVar_ID_106190 Human_SNP_ID_308193718 m1A Human chr7 + 4759403 4759403 4759403 TGGCCAAGCCCGTGGCCTACATGCCCGCCTCCATCGTAACCTCACAGCAGCCCGCGGGCCACGCC TGGCCAAGCCCGTGGCCTACATGCCCGCCTCCCTCGTAACCTCACAGCAGCCCGCGGGCCACGCC A C FOXK1 Ensembl:ENSG00000164916 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:4759303..4759440 26863196 MeRIP-seq:(Medium) rs1211942469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685310,Human_RBP_ID_26830113,Human_RBP_ID_27114257 Human_Splice_Rec_839736,Human_Splice_Rec_839744 RMVar_hsa_circ_72499,RMVar_hsa_circ_46595,RMVar_hsa_circ_25601 106191 RMVar_ID_106191 Human_SNP_ID_308195846 m1A Human chr7 + 4765108 4765108 4765108 GGATGAAGGGACGTGGTCCTAGGGGTCGGCTCAGACTCGGAGCAGGGCAGGGAGAGGAGGGCAAG GGATGAAGGGACGTGGTCCTAGGGGTCGGCTCGGACTCGGAGCAGGGCAGGGAGAGGAGGGCAAG A G FOXK1 Ensembl:ENSG00000164916 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:4764966..4765186 26863196 MeRIP-seq:(Medium) rs1255946016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860406,Human_RBP_ID_5328344,Human_RBP_ID_7743753,Human_RBP_ID_8911564,Human_RBP_ID_16170290,Human_RBP_ID_22728776,Human_RBP_ID_26550301,Human_RBP_ID_27532097 106192 RMVar_ID_106192 Human_SNP_ID_308201764 m1A Human chr7 - 4781242 4781242 4781242 CCTCTGCAGGGAGTCGAGGGTGTCCGGCCCCAAGTCCTCCGCCTGCAGCAGTTTACAGATCCGGG CCTCTGCAGGGAGTCGAGGGTGTCCGGCCCCATGTCCTCCGCCTGCAGCAGTTTACAGATCCGGG T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:4781161..4781260 26863196 MeRIP-seq:(Medium) rs1346180789 Functional Loss SNV dbSNP153 33..33 33 - - - 106193 RMVar_ID_106193 Human_SNP_ID_308201768 m1A Human chr7 + 4781252 4781252 4781252 TAAACTGCTGCAGGCGGAGGACTTGGGGCCGGACACCCTCGACTCCCTGCAGAGGCTCTTCCTCA TAAACTGCTGCAGGCGGAGGACTTGGGGCCGGCCACCCTCGACTCCCTGCAGAGGCTCTTCCTCA A C AP5Z1 Ensembl:ENSG00000242802 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:4781164..4781264;chr7:4781164..4781275 26863196 MeRIP-seq:(Medium) rs371093286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253919 Human_Splice_Rec_839748,Human_Splice_Rec_839749,Human_Splice_Rec_839778,Human_Splice_Rec_839779,Human_Splice_Rec_839836,Human_Splice_Rec_839837,Human_Splice_Rec_839842,Human_Splice_Rec_839843,Human_Splice_Rec_839874,Human_Splice_Rec_839875 RMVar_hsa_circ_243450,RMVar_hsa_circ_300081 106194 RMVar_ID_106194 Human_SNP_ID_308201769 m1A Human chr7 + 4781252 4781252 4781252 TAAACTGCTGCAGGCGGAGGACTTGGGGCCGGACACCCTCGACTCCCTGCAGAGGCTCTTCCTCA TAAACTGCTGCAGGCGGAGGACTTGGGGCCGGGCACCCTCGACTCCCTGCAGAGGCTCTTCCTCA A G AP5Z1 Ensembl:ENSG00000242802 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:4781164..4781264;chr7:4781164..4781275 26863196 MeRIP-seq:(Medium) rs371093286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253919 Human_Splice_Rec_839748,Human_Splice_Rec_839749,Human_Splice_Rec_839778,Human_Splice_Rec_839779,Human_Splice_Rec_839836,Human_Splice_Rec_839837,Human_Splice_Rec_839842,Human_Splice_Rec_839843,Human_Splice_Rec_839874,Human_Splice_Rec_839875 RMVar_hsa_circ_243450,RMVar_hsa_circ_300081 106195 RMVar_ID_106195 Human_SNP_ID_308201922 m1A Human chr7 + 4781548 4781548 4781548 CCTGCCACGGTCGTGACGTGTTACCGCCCACCACGGGCATCTCGCCTTCCAGGCTGGAGAAGACA CCTGCCACGGTCGTGACGTGTTACCGCCCACCCCGGGCATCTCGCCTTCCAGGCTGGAGAAGACA A C AP5Z1 Ensembl:ENSG00000242802 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4781545..4781644 26863196 MeRIP-seq:(Medium) rs748224359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243450,RMVar_hsa_circ_300081 106196 RMVar_ID_106196 Human_SNP_ID_308202745 m1A Human chr7 - 4783410 4783410 4783410 GGCTGAGGACCACGACCTTGGCCATGACGGGGAGGAGGTGTCTGAGGCTGGGTCCCTCAGGCTGC GGCTGAGGACCACGACCTTGGCCATGACGGGGTGGAGGTGTCTGAGGCTGGGTCCCTCAGGCTGC T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4783360..4783439 26863196 MeRIP-seq:(Medium) rs199942388 Functional Loss SNV dbSNP153 33..33 33 - - - 106197 RMVar_ID_106197 Human_SNP_ID_308204118 m1A Human chr7 - 4785676 4785676 4785676 AGCGCCACCCCACCCTGGGCTCACCGTGGCTCAGGAAGAAGTGGGCGAGGGGCAGCAGCACCCGC AGCGCCACCCCACCCTGGGCTCACCGTGGCTCTGGAAGAAGTGGGCGAGGGGCAGCAGCACCCGC T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:4784255..4785675 32194978 MeRIP-seq:(Medium) rs11772411 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_679 106198 RMVar_ID_106198 Human_SNP_ID_308205464 m1A Human chr7 + 4788181 4788181 4788181 CGCAGGTCAGCACCGGCTGCATCCGAGAGGCCACTCTGGGACACCTCTCTCAGGGCCCCCAGCTG CGCAGGTCAGCACCGGCTGCATCCGAGAGGCCGCTCTGGGACACCTCTCTCAGGGCCCCCAGCTG A G AP5Z1 Ensembl:ENSG00000242802 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:4787755..4788332 32194978 MeRIP-seq:(Medium) rs755447421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793937,Human_RBP_ID_954149,Human_RBP_ID_19134612 Human_Splice_Rec_839766,Human_Splice_Rec_839798,Human_Splice_Rec_839826,Human_Splice_Rec_839862,Human_Splice_Rec_839894,Human_Splice_Rec_839920,Human_Splice_Rec_839956,Human_Splice_Rec_839970,Human_Splice_Rec_839986,Human_Splice_Rec_839998,Human_Splice_Rec_840002 Human_miRNA_ID_1972719 RMVar_hsa_circ_82011,RMVar_hsa_circ_243452 106199 RMVar_ID_106199 Human_SNP_ID_308207729 m1A Human chr7 + 4791374 4791374 4791374 TCAGCCGGCTGGTGGAGAGGGAGGCCGGCCTCATGCCAGGGTGAAGGGACAGTGGCCAGGGACTT TCAGCCGGCTGGTGGAGAGGGAGGCCGGCCTCTTGCCAGGGTGAAGGGACAGTGGCCAGGGACTT A T AP5Z1 Ensembl:ENSG00000242802 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:4791323..4791623 32194978 MeRIP-seq:(Medium) rs1228243492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844181,Human_RBP_ID_8668389 RMVar_hsa_circ_82011,RMVar_hsa_circ_243452 106200 RMVar_ID_106200 Human_SNP_ID_308207839 m1A Human chr7 + 4791575 4791575 4791575 CCCCCCTGCTCACCCTCTGGGCTTTGTCTCCGAGCCTTTTGCTCCCAGGCAACACTGAGCTGAGC CCCCCCTGCTCACCCTCTGGGCTTTGTCTCCGCGCCTTTTGCTCCCAGGCAACACTGAGCTGAGC A C AP5Z1 Ensembl:ENSG00000242802 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:4791525..4791747 26863196 MeRIP-seq:(Medium) rs1232009202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18171862 RMVar_hsa_circ_82011,RMVar_hsa_circ_243452 106201 RMVar_ID_106201 Human_SNP_ID_308211519 m1A Human chr7 + 4799442 4799442 4799442 TGGCTGTTTCCACGTCGGACTTCGCGACCAGGAACCGCATCTTCTTCCCGCCATGACGGATCAGG TGGCTGTTTCCACGTCGGACTTCGCGACCAGGCACCGCATCTTCTTCCCGCCATGACGGATCAGG A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:4799391..4800238 32194978 MeRIP-seq:(Medium) rs1347902547 Functional Loss SNV dbSNP153 33..33 33 - - - 106202 RMVar_ID_106202 Human_SNP_ID_308269716 m1A Human chr7 - 4974140 4974140 4974140 CCGACACTCACTCGCCACTCAACTCGCCGGCTAGCCAGGCGGGTTCGGCGACCTTCGCTACCACG CCGACACTCACTCGCCACTCAACTCGCCGGCTGGCCAGGCGGGTTCGGCGACCTTCGCTACCACG T C RF00017-4706,RF00017-4567,RF00017-4567:2,RF00017-4489 RNACentral:URS0000954994,RNACentral:URS000093B3AD,RNACentral:URS000094CDE3,RNACentral:URS00009982F9 SRP RNA,SRP RNA,SRP RNA,SRP RNA intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:4974092..4974215 26863196 MeRIP-seq:(Medium) rs1309619539 Functional Loss SNV dbSNP153 33..33 33 - - - 106203 RMVar_ID_106203 Human_SNP_ID_308277949 m1A Human chr7 + 4999005 4999005 4999005 GAGGTGCAGCTAGTGGGAGCCTAGGGCGTCGGAGAAGGATGACCAGAGGGCTTGGGGGCAGGAGT GAGGTGCAGCTAGTGGGAGCCTAGGGCGTCGGGGAAGGATGACCAGAGGGCTTGGGGGCAGGAGT A G RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4998996..4999150 26863196 MeRIP-seq:(Medium) rs1431503961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7744127,Human_RBP_ID_16171301,Human_RBP_ID_17674076,Human_RBP_ID_18541174 106204 RMVar_ID_106204 Human_SNP_ID_308288079 m1A Human chr7 - 5032997 5032995 5032997 GTTTGTGTTTTCTGTCTGGGTGTCCCACACACATGTGGTTCTGAAGGGAAGGACCCATTCCTTGA GTTTGTGTTTTCTGTCTGGGTGTCCCACACAC__GTGGTTCTGAAGGGAAGGACCCATTCCTTGA CAT C SPDYE19P Ensembl:ENSG00000275328 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5032981..5033116 26863196 MeRIP-seq:(Medium) rs967647118 Functional Loss DEL dbSNP153 33..34 33 - - - 106205 RMVar_ID_106205 Human_SNP_ID_308288082 m1A Human chr7 - 5032997 5032997 5032997 GTTTGTGTTTTCTGTCTGGGTGTCCCACACACATGTGGTTCTGAAGGGAAGGACCCATTCCTTGA GTTTGTGTTTTCTGTCTGGGTGTCCCACACACGTGTGGTTCTGAAGGGAAGGACCCATTCCTTGA T C SPDYE19P Ensembl:ENSG00000275328 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5032981..5033116 26863196 MeRIP-seq:(Medium) rs1256693800 Functional Loss SNV dbSNP153 33..33 33 - - - 106206 RMVar_ID_106206 Human_SNP_ID_308291975 m1A Human chr7 + 5045963 5045963 5045963 GAGAATCGCGGAGCCTGCGGGGCTGGAGGTTGAGCGCCCGGGCCAGCACCTAGGCGGGCGCGGGG GAGAATCGCGGAGCCTGCGGGGCTGGAGGTTGGGCGCCCGGGCCAGCACCTAGGCGGGCGCGGGG A G RBAK-RBAKDN,RBAK Ensembl:ENSG00000272968,Ensembl:ENSG00000146587 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5045914..5046194 26863196 MeRIP-seq:(Medium) rs1276847389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13687,Human_RBP_ID_4956141,Human_RBP_ID_5152892,Human_RBP_ID_16173316,Human_RBP_ID_18425956,Human_RBP_ID_26772188 RMVar_hsa_circ_121990,RMVar_hsa_circ_243462 106207 RMVar_ID_106207 Human_SNP_ID_308342285 m1A Human chr7 + 5191611 5191609 5191611 GGGGATGGTTAATAGATGAGCGAGCTTTCTGGAGAGAGAAGGGTGAGTTATGGGGTTGGCAGGGA GGGGATGGTTAATAGATGAGCGAGCTTTCTG__GAGAGAAGGGTGAGTTATGGGGTTGGCAGGGA GGA G WIPI2 Ensembl:ENSG00000157954 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5191607..5191761 26863196 MeRIP-seq:(Medium) rs759384137 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106208 RMVar_ID_106208 Human_SNP_ID_308353419 m1A Human chr7 + 5225887 5225887 5225887 TGGACGGCATGTTCCTCTCCGCCTCCAGCAACACTGAGACCGTGCACATCTTCAAACTCGAGACT TGGACGGCATGTTCCTCTCCGCCTCCAGCAACGCTGAGACCGTGCACATCTTCAAACTCGAGACT A G WIPI2 Ensembl:ENSG00000157954 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:5225837..5225988 32194978 MeRIP-seq:(Medium) rs1383333000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685714,Human_RBP_ID_793681,Human_RBP_ID_16174719 Human_Splice_Rec_840358,Human_Splice_Rec_840359,Human_Splice_Rec_840382,Human_Splice_Rec_840383,Human_Splice_Rec_840406,Human_Splice_Rec_840407,Human_Splice_Rec_840430,Human_Splice_Rec_840431,Human_Splice_Rec_840458,Human_Splice_Rec_840459,Human_Splice_Rec_840492,Human_Splice_Rec_840493,Human_Splice_Rec_840518,Human_Splice_Rec_840528 RMVar_hsa_circ_9111,RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_354182,RMVar_hsa_circ_89918,RMVar_hsa_circ_112526,RMVar_hsa_circ_6811,RMVar_hsa_circ_91830,RMVar_hsa_circ_322156,RMVar_hsa_circ_243470,RMVar_hsa_circ_32225,RMVar_hsa_circ_243473,RMVar_hsa_circ_106030,RMVar_hsa_circ_243474,RMVar_hsa_circ_243475 106209 RMVar_ID_106209 Human_SNP_ID_308353905 m1A Human chr7 + 5227339 5227339 5227339 CCATTCTGCGGCCACAAAAACATCTGCTCGCTAGCCACGTGAGTAGAGCCGGCGCCTCCGTCCCC CCATTCTGCGGCCACAAAAACATCTGCTCGCTGGCCACGTGAGTAGAGCCGGCGCCTCCGTCCCC A G WIPI2 Ensembl:ENSG00000157954 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:5227209..5227416 26863196 MeRIP-seq:(Medium) rs766146632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26831096 Human_Splice_Rec_840361,Human_Splice_Rec_840385,Human_Splice_Rec_840409,Human_Splice_Rec_840433,Human_Splice_Rec_840461,Human_Splice_Rec_840495,Human_Splice_Rec_840529 RMVar_hsa_circ_9111,RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_89918,RMVar_hsa_circ_112526,RMVar_hsa_circ_6811,RMVar_hsa_circ_91830,RMVar_hsa_circ_243470,RMVar_hsa_circ_32225,RMVar_hsa_circ_243473,RMVar_hsa_circ_106030,RMVar_hsa_circ_243474,RMVar_hsa_circ_243475 106210 RMVar_ID_106210 Human_SNP_ID_308355567 m1A Human chr7 + 5231881 5231881 5231881 CGCTGTCCGCAGGGGCTTCCTACCTGTGTGAGAGGTCGTAGCGGGAGACAGCAACAGAGAGTAGG CGCTGTCCGCAGGGGCTTCCTACCTGTGTGAGTGGTCGTAGCGGGAGACAGCAACAGAGAGTAGG A T WIPI2 Ensembl:ENSG00000157954 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:5231830..5232031 32194978 MeRIP-seq:(Medium) rs1334625924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685750,Human_RBP_ID_16174841,Human_RBP_ID_18101852,Human_RBP_ID_24218956,Human_RBP_ID_27532329 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_112526,RMVar_hsa_circ_243473 106211 RMVar_ID_106211 Human_SNP_ID_308372467 m1A Human chr7 - 5282943 5282943 5282943 CGGCCCCGGTCCACGAGCGCGGCGACGAGCACAGCCCAGGCCACCACGCCCCGCCTCTGCCCGCC CGGCCCCGGTCCACGAGCGCGGCGACGAGCACCGCCCAGGCCACCACGCCCCGCCTCTGCCCGCC T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5282934..5283130 26863196 MeRIP-seq:(Medium) rs1160498019 Functional Loss SNV dbSNP153 33..33 33 - - - 106212 RMVar_ID_106212 Human_SNP_ID_308374527 m1A Human chr7 - 5287786 5287784 5287786 ATGGCAGCCTCTGCTTTGGAGAAAGCAGAGAGAGCAGGTGAGGGAAGAAGGCTGAGGGATCCATG ATGGCAGCCTCTGCTTTGGAGAAAGCAGAGAG__CAGGTGAGGGAAGAAGGCTGAGGGATCCATG GCT G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5287782..5287905 26863196 MeRIP-seq:(Medium) rs752725965 Functional Loss DEL dbSNP153 33..34 33 - - - 106213 RMVar_ID_106213 Human_SNP_ID_308375809 m1A Human chr7 - 5290735 5290735 5290735 CGTGATAACGGTCATCGGGCACTGGCTCGTCCAATGCTAAAGCCAGAGACACCAGGTGAGACGGG CGTGATAACGGTCATCGGGCACTGGCTCGTCCGATGCTAAAGCCAGAGACACCAGGTGAGACGGG T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5283054..5290773 32194978 MeRIP-seq:(Medium) rs201447711 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 106214 RMVar_ID_106214 Human_SNP_ID_308378406 m1A Human chr7 - 5296868 5296868 5296868 GCCCAGCTCCCTGCACCGCCCCGTCCCGCCCCAGCCCCGTCCACACACAGACCCCTCCCCACCGG GCCCAGCTCCCTGCACCGCCCCGTCCCGCCCCCGCCCCGTCCACACACAGACCCCTCCCCACCGG T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5296864..5296947 26863196 MeRIP-seq:(Medium) rs1417126937 Functional Loss SNV dbSNP153 33..33 33 - - - 106215 RMVar_ID_106215 Human_SNP_ID_308379893 m1A Human chr7 - 5299420 5299420 5299420 ACACCGGGCAGGGCAGGCAGCCCACCTTGCCCACGAAGTCTGACAGGTTGAACACAGCCATGATG ACACCGGGCAGGGCAGGCAGCCCACCTTGCCCGCGAAGTCTGACAGGTTGAACACAGCCATGATG T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5299371..5300465 32194978 MeRIP-seq:(Medium) rs769919552 Functional Loss SNV dbSNP153 33..33 33 - - - 106216 RMVar_ID_106216 Human_SNP_ID_308380412 m1A Human chr7 + 5300524 5300524 5300524 TCATCCCCCTCTTCATCCTGTGCGTCTACCCCAGCGGCATGCCCGCCCTCCGTCACCCCGCCTGG TCATCCCCCTCTTCATCCTGTGCGTCTACCCCGGCGGCATGCCCGCCCTCCGTCACCCCGCCTGG A G SLC29A4 Ensembl:ENSG00000164638 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5299321..5300614 26863196 MeRIP-seq:(Medium) rs753929061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793723,Human_RBP_ID_18959909 Human_miRNA_ID_2683813,Human_miRNA_ID_2683814,Human_miRNA_ID_2683815 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_91264,RMVar_hsa_circ_118800,RMVar_hsa_circ_243476,RMVar_hsa_circ_243481,RMVar_hsa_circ_105360,RMVar_hsa_circ_243484 106217 RMVar_ID_106217 Human_SNP_ID_308381751 m1A Human chr7 - 5303543 5303543 5303543 GCTGTGGTTTCCCAGAGGCTGATGCAGACCGCAGGCGGGTCCATTCGGACCCAGGGCTCCGACTC GCTGTGGTTTCCCAGAGGCTGATGCAGACCGCCGGCGGGTCCATTCGGACCCAGGGCTCCGACTC T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5303492..5303593 32194978 MeRIP-seq:(Medium) rs1029161763 Functional Loss SNV dbSNP153 33..33 33 - - - 106218 RMVar_ID_106218 Human_SNP_ID_308383336 m1A Human chr7 - 5307109 5307101 5307110 CGGCCTCCCAGTCCCCAGCACACCCCCCGCCCACCCCACCAAGTGTACTGTACTCACCCCCCAGG CGGCCTCCCAGTCCCCAGCACACCCCCCGCC_________AAGTGTACTGTACTCACCCCCCAGG TGGTGGGGTG T TNRC18 Ensembl:ENSG00000182095 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1015194422 Functional Loss DEL dbSNP153 32..40 33 - - - 106219 RMVar_ID_106219 Human_SNP_ID_308383345 m1A Human chr7 - 5307109 5307109 5307109 CGGCCTCCCAGTCCCCAGCACACCCCCCGCCCACCCCACCAAGTGTACTGTACTCACCCCCCAGG CGGCCTCCCAGTCCCCAGCACACCCCCCGCCCCCCCCACCAAGTGTACTGTACTCACCCCCCAGG T G TNRC18 Ensembl:ENSG00000182095 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs955688031 Functional Loss SNV dbSNP153 33..33 33 - - - 106220 RMVar_ID_106220 Human_SNP_ID_308386414 m1A Human chr7 + 5313108 5313108 5313108 GGCAGCGCTGCAGTTACGGCCCCCGGTGCCGCAGCCCCCGTCCCCGTTCTTGTCGCCTTCCTCCT GGCAGCGCTGCAGTTACGGCCCCCGGTGCCGCGGCCCCCGTCCCCGTTCTTGTCGCCTTCCTCCT A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5313072..5313317 26863196 MeRIP-seq:(Medium) rs1219573338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106221 RMVar_ID_106221 Human_SNP_ID_308386862 m1A Human chr7 - 5313728 5313728 5313728 AGAGCCTGTGGACAAGCGAGCCAAGGCCCCCAAGGCGCGCCCGGCACCGCCGCAGCCCAGTCCCG AGAGCCTGTGGACAAGCGAGCCAAGGCCCCCAGGGCGCGCCCGGCACCGCCGCAGCCCAGTCCCG T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5313576..5313906 26863196 MeRIP-seq:(Medium) rs771097631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_39138,RMVar_hsa_circ_115634,RMVar_hsa_circ_34969 106222 RMVar_ID_106222 Human_SNP_ID_308386863 m1A Human chr7 - 5313729 5313729 5313729 CAGAGCCTGTGGACAAGCGAGCCAAGGCCCCCAAGGCGCGCCCGGCACCGCCGCAGCCCAGTCCC CAGAGCCTGTGGACAAGCGAGCCAAGGCCCCCGAGGCGCGCCCGGCACCGCCGCAGCCCAGTCCC T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:5313633..5313742 26863410 MeRIP-seq:(Medium) rs757585097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_39138,RMVar_hsa_circ_115634,RMVar_hsa_circ_34969 106223 RMVar_ID_106223 Human_SNP_ID_308387351 m1A Human chr7 + 5314942 5314942 5314942 GTTCCCAAGCCCTGAGTTTGGATGCACGAAGGAGATCCGCCCACCGCCCTGCCCTGGGGACCAGG GTTCCCAAGCCCTGAGTTTGGATGCACGAAGGGGATCCGCCCACCGCCCTGCCCTGGGGACCAGG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5314939..5315054 26863196 MeRIP-seq:(Medium) rs1417584213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106224 RMVar_ID_106224 Human_SNP_ID_308387397 m1A Human chr7 - 5315033 5315033 5315033 GATGGTGGCACGGCTGGGTCGGAGGAGCCAGGAGCCAAGGCCCGTGGGCGTGGGCGGAAACCCAG GATGGTGGCACGGCTGGGTCGGAGGAGCCAGGGGCCAAGGCCCGTGGGCGTGGGCGGAAACCCAG T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5314916..5315045 26863196 MeRIP-seq:(Medium) rs758843327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9311720,Human_RBP_ID_19019426 Human_Splice_Rec_840667,Human_Splice_Rec_840725,Human_Splice_Rec_840739 RMVar_hsa_circ_437,RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_39138,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_243486 106225 RMVar_ID_106225 Human_SNP_ID_308387398 m1A Human chr7 - 5315033 5315033 5315033 GATGGTGGCACGGCTGGGTCGGAGGAGCCAGGAGCCAAGGCCCGTGGGCGTGGGCGGAAACCCAG GATGGTGGCACGGCTGGGTCGGAGGAGCCAGGCGCCAAGGCCCGTGGGCGTGGGCGGAAACCCAG T G TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5314916..5315045 26863196 MeRIP-seq:(Medium) rs758843327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9311720,Human_RBP_ID_19019426 Human_Splice_Rec_840667,Human_Splice_Rec_840725,Human_Splice_Rec_840739 RMVar_hsa_circ_437,RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_39138,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_243486 106226 RMVar_ID_106226 Human_SNP_ID_308390158 m1A Human chr7 - 5323191 5323188 5323191 AAATCGTGGGTATGGATGGGGGAGCGAGTGAGAAGGAGTCGGCCGCCCCAAGGCTGCATTGGTCA AAATCGTGGGTATGGATGGGGGAGCGAGTGAG___GAGTCGGCCGCCCCAAGGCTGCATTGGTCA CCTT C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5323180..5323340 26863196 MeRIP-seq:(Medium) rs915100863 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_18063,RMVar_hsa_circ_120768,RMVar_hsa_circ_243486,RMVar_hsa_circ_378437,RMVar_hsa_circ_243487,RMVar_hsa_circ_46491 106227 RMVar_ID_106227 Human_SNP_ID_308390160 m1A Human chr7 - 5323191 5323191 5323191 AAATCGTGGGTATGGATGGGGGAGCGAGTGAGAAGGAGTCGGCCGCCCCAAGGCTGCATTGGTCA AAATCGTGGGTATGGATGGGGGAGCGAGTGAGGAGGAGTCGGCCGCCCCAAGGCTGCATTGGTCA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5323180..5323340 26863196 MeRIP-seq:(Medium) rs945177085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46231,RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_18063,RMVar_hsa_circ_120768,RMVar_hsa_circ_243486,RMVar_hsa_circ_378437,RMVar_hsa_circ_243487,RMVar_hsa_circ_46491 106228 RMVar_ID_106228 Human_SNP_ID_308393605 m1A Human chr7 - 5332589 5332589 5332589 GTAGGGGCCGCGCTGGGAGGGGGTGCCGCAGAAGGGTCCCTGGGGTTCCGTGAGGGAGGGGCCCT GTAGGGGCCGCGCTGGGAGGGGGTGCCGCAGATGGGTCCCTGGGGTTCCGTGAGGGAGGGGCCCT T A TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5332587..5332688 26863196 MeRIP-seq:(Medium) rs1205131204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5403764,Human_RBP_ID_22554593,Human_RBP_ID_26794310 RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_120768,RMVar_hsa_circ_243486,RMVar_hsa_circ_378437,RMVar_hsa_circ_243487,RMVar_hsa_circ_72905,RMVar_hsa_circ_46491,RMVar_hsa_circ_332209,RMVar_hsa_circ_284167,RMVar_hsa_circ_243489 106229 RMVar_ID_106229 Human_SNP_ID_308393606 m1A Human chr7 - 5332589 5332589 5332589 GTAGGGGCCGCGCTGGGAGGGGGTGCCGCAGAAGGGTCCCTGGGGTTCCGTGAGGGAGGGGCCCT GTAGGGGCCGCGCTGGGAGGGGGTGCCGCAGAGGGGTCCCTGGGGTTCCGTGAGGGAGGGGCCCT T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5332587..5332688 26863196 MeRIP-seq:(Medium) rs1205131204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5403764,Human_RBP_ID_22554593,Human_RBP_ID_26794310 RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_120768,RMVar_hsa_circ_243486,RMVar_hsa_circ_378437,RMVar_hsa_circ_243487,RMVar_hsa_circ_72905,RMVar_hsa_circ_46491,RMVar_hsa_circ_332209,RMVar_hsa_circ_284167,RMVar_hsa_circ_243489 106230 RMVar_ID_106230 Human_SNP_ID_308393840 m1A Human chr7 - 5332949 5332949 5332949 CTGCGGCCCAAGAAGGGGCTGGGGGAGCCGGGACCCTCCCTGGCCGCACCCACGCCTGGCGCCCG CTGCGGCCCAAGAAGGGGCTGGGGGAGCCGGGCCCCTCCCTGGCCGCACCCACGCCTGGCGCCCG T G TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5332901..5332998 26863196 MeRIP-seq:(Medium) rs1386888663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5153577 RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_268429,RMVar_hsa_circ_48417,RMVar_hsa_circ_36470,RMVar_hsa_circ_120768,RMVar_hsa_circ_243486,RMVar_hsa_circ_378437,RMVar_hsa_circ_243487,RMVar_hsa_circ_72905,RMVar_hsa_circ_46491,RMVar_hsa_circ_332209,RMVar_hsa_circ_284167,RMVar_hsa_circ_243489,RMVar_hsa_circ_105174,RMVar_hsa_circ_268646,RMVar_hsa_circ_243490,RMVar_hsa_circ_27010 106231 RMVar_ID_106231 Human_SNP_ID_308398298 m1A Human chr7 + 5345526 5345521 5345526 TGTGGGATGGGGCAATGGCGTCCGCCCCTCCCACCCACCCCCACCGCAGCCCACCTGCTGCCACT TGTGGGATGGGGCAATGGCGTCCGCCCC_____CCCACCCCCACCGCAGCCCACCTGCTGCCACT CTCCCA C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5345523..5345631 26863196 MeRIP-seq:(Medium) rs752620498 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106232 RMVar_ID_106232 Human_SNP_ID_308398303 m1A Human chr7 + 5345526 5345526 5345526 TGTGGGATGGGGCAATGGCGTCCGCCCCTCCCACCCACCCCCACCGCAGCCCACCTGCTGCCACT TGTGGGATGGGGCAATGGCGTCCGCCCCTCCCCCCCACCCCCACCGCAGCCCACCTGCTGCCACT A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5345523..5345631 26863196 MeRIP-seq:(Medium) rs761317950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106233 RMVar_ID_106233 Human_SNP_ID_308404630 m1A Human chr7 - 5361707 5361707 5361707 GTGTGATTCTTTTTAAGGGACAGGCGCGAGGAACCCCATAGAAGCTTGGCACGCAGAGGCCCTGG GTGTGATTCTTTTTAAGGGACAGGCGCGAGGAGCCCCATAGAAGCTTGGCACGCAGAGGCCCTGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5361657..5361768 26863196 MeRIP-seq:(Medium) rs1343940504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954171,Human_RBP_ID_9404240 Human_Splice_Rec_840642,Human_Splice_Rec_840700 RMVar_hsa_circ_268487,RMVar_hsa_circ_243485,RMVar_hsa_circ_115634,RMVar_hsa_circ_99548,RMVar_hsa_circ_264797,RMVar_hsa_circ_243486,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_27010,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_61639,RMVar_hsa_circ_72939,RMVar_hsa_circ_1145,RMVar_hsa_circ_111587,RMVar_hsa_circ_350305,RMVar_hsa_circ_243496 106234 RMVar_ID_106234 Human_SNP_ID_308404783 m1A Human chr7 + 5361993 5361993 5361993 CCTCGGCCAGCCGCATCCGGAAGTCCAGCTCCAGGGCGTCCATGTCCTCCAGGGAGGACTTCATG CCTCGGCCAGCCGCATCCGGAAGTCCAGCTCCGGGGCGTCCATGTCCTCCAGGGAGGACTTCATG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5361943..5362054 26863196 MeRIP-seq:(Medium) rs1240172957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106235 RMVar_ID_106235 Human_SNP_ID_308407872 m1A Human chr7 + 5370367 5370367 5370367 ACTCACGAATCTGCAGAACTCAGAGGTCGCGCACTCTCACCTCCCATCTCTTGGCTCCTCCTCTC ACTCACGAATCTGCAGAACTCAGAGGTCGCGCGCTCTCACCTCCCATCTCTTGGCTCCTCCTCTC A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5370365..5370472 26863196 MeRIP-seq:(Medium) rs1016775136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106236 RMVar_ID_106236 Human_SNP_ID_308407875 m1A Human chr7 - 5370376 5370376 5370376 CTGGAGCTGGAGAGGAGGAGCCAAGAGATGGGAGGTGAGAGTGCGCGACCTCTGAGTTCTGCAGA CTGGAGCTGGAGAGGAGGAGCCAAGAGATGGGTGGTGAGAGTGCGCGACCTCTGAGTTCTGCAGA T A TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5370368..5370625 26863196 MeRIP-seq:(Medium) rs1346635580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954176,Human_RBP_ID_3971812,Human_RBP_ID_5533397,Human_RBP_ID_5622978,Human_RBP_ID_8914280,Human_RBP_ID_9311190,Human_RBP_ID_9403131,Human_RBP_ID_17713256,Human_RBP_ID_18472287,Human_RBP_ID_19134647,Human_RBP_ID_24554932 Human_Splice_Rec_840637,Human_Splice_Rec_840695 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106237 RMVar_ID_106237 Human_SNP_ID_308408046 m1A Human chr7 - 5370731 5370731 5370731 AGGCCTGGCGCAGGTGGCACCGAGCGAGTCCCAGCCCACCCTAGAAATGTCAGACTGTGACGTGC AGGCCTGGCGCAGGTGGCACCGAGCGAGTCCCGGCCCACCCTAGAAATGTCAGACTGTGACGTGC T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5370683..5370880 26863196 MeRIP-seq:(Medium) rs1477882477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5533400,Human_RBP_ID_8914284,Human_RBP_ID_9311747,Human_RBP_ID_26357541,Human_RBP_ID_27532405 Human_miRNA_ID_164054,Human_miRNA_ID_711218,Human_miRNA_ID_718492,Human_miRNA_ID_1705700,Human_miRNA_ID_2872944,Human_miRNA_ID_2980909 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106238 RMVar_ID_106238 Human_SNP_ID_308408060 m1A Human chr7 - 5370745 5370745 5370745 GCAGTGCCCGAGGAAGGCCTGGCGCAGGTGGCACCGAGCGAGTCCCAGCCCACCCTAGAAATGTC GCAGTGCCCGAGGAAGGCCTGGCGCAGGTGGCTCCGAGCGAGTCCCAGCCCACCCTAGAAATGTC T A TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5370695..5370780 26863196 MeRIP-seq:(Medium) rs755144997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955975,Human_RBP_ID_5533400,Human_RBP_ID_8911905,Human_RBP_ID_9263413,Human_RBP_ID_9311747,Human_RBP_ID_18466491,Human_RBP_ID_26357541,Human_RBP_ID_27532405 Human_miRNA_ID_1705700,Human_miRNA_ID_2590018 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106239 RMVar_ID_106239 Human_SNP_ID_308408080 m1A Human chr7 - 5370779 5370779 5370779 GGTGGAGGTGCCTGTGGCGGTGCCCGTGGTGGAGGCAGTGCCCGAGGAAGGCCTGGCGCAGGTGG GGTGGAGGTGCCTGTGGCGGTGCCCGTGGTGGTGGCAGTGCCCGAGGAAGGCCTGGCGCAGGTGG T A TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5370606..5370805 26863196 MeRIP-seq:(Medium) rs1417686346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955975,Human_RBP_ID_3971814,Human_RBP_ID_5533400,Human_RBP_ID_8914284,Human_RBP_ID_9263413,Human_RBP_ID_9311748,Human_RBP_ID_18466491,Human_RBP_ID_26357541 Human_miRNA_ID_1965659 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106240 RMVar_ID_106240 Human_SNP_ID_308408081 m1A Human chr7 - 5370779 5370779 5370779 GGTGGAGGTGCCTGTGGCGGTGCCCGTGGTGGAGGCAGTGCCCGAGGAAGGCCTGGCGCAGGTGG GGTGGAGGTGCCTGTGGCGGTGCCCGTGGTGGGGGCAGTGCCCGAGGAAGGCCTGGCGCAGGTGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5370606..5370805 26863196 MeRIP-seq:(Medium) rs1417686346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955975,Human_RBP_ID_3971814,Human_RBP_ID_5533400,Human_RBP_ID_8914284,Human_RBP_ID_9263413,Human_RBP_ID_9311748,Human_RBP_ID_18466491,Human_RBP_ID_26357541 Human_miRNA_ID_1965659 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106241 RMVar_ID_106241 Human_SNP_ID_308408425 m1A Human chr7 - 5371339 5371339 5371339 TTGGCAGATATCCCGCCCAGGTACCCGTTCCAAGCCCTGCCACCGCACTACGGGAGGCCCTACCC TTGGCAGATATCCCGCCCAGGTACCCGTTCCACGCCCTGCCACCGCACTACGGGAGGCCCTACCC T G TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5371108..5371386 26863196 MeRIP-seq:(Medium) rs1459081256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_953542,Human_RBP_ID_18196246 Human_Splice_Rec_840636,Human_Splice_Rec_840694 RMVar_hsa_circ_268487,RMVar_hsa_circ_264797,RMVar_hsa_circ_9980,RMVar_hsa_circ_72905,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_340729,RMVar_hsa_circ_18436,RMVar_hsa_circ_72939,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_270119,RMVar_hsa_circ_306536,RMVar_hsa_circ_243497 106242 RMVar_ID_106242 Human_SNP_ID_308411194 m1A Human chr7 - 5378021 5378021 5378021 GGGGCTCACTTCCACCTGGCCCCCTGCAGGGCACGGCCGAGCAGATGAGGACTGTGTGGACGACC GGGGCTCACTTCCACCTGGCCCCCTGCAGGGCGCGGCCGAGCAGATGAGGACTGTGTGGACGACC T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:5377991..5378065;chr7:5378011..5378096 26863196 MeRIP-seq:(Medium) rs1485751947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955985,Human_RBP_ID_19019430,Human_RBP_ID_22554598,Human_RBP_ID_26794321 Human_Splice_Rec_840626,Human_Splice_Rec_840627,Human_Splice_Rec_840684,Human_Splice_Rec_840685,Human_Splice_Rec_840758,Human_Splice_Rec_840759 RMVar_hsa_circ_268487,RMVar_hsa_circ_9980,RMVar_hsa_circ_15667,RMVar_hsa_circ_18436,RMVar_hsa_circ_39440,RMVar_hsa_circ_26523,RMVar_hsa_circ_306536,RMVar_hsa_circ_348653,RMVar_hsa_circ_341853,RMVar_hsa_circ_51740,RMVar_hsa_circ_243498,RMVar_hsa_circ_62735 106243 RMVar_ID_106243 Human_SNP_ID_308414681 m1A Human chr7 - 5387769 5387769 5387769 GCAGAAGTGCGACACCCGCCTGTGGGCATTGCAGTGGCTGTGGCCCGGCAGAAGGACAGTGGCGG GCAGAAGTGCGACACCCGCCTGTGGGCATTGCGGTGGCTGTGGCCCGGCAGAAGGACAGTGGCGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5377937..5387785 32194978 MeRIP-seq:(Medium) rs1033937451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1052491,Human_RBP_ID_8911936,Human_RBP_ID_9311197,Human_RBP_ID_22112501,Human_RBP_ID_22730178,Human_RBP_ID_27532435 Human_Splice_Rec_840625,Human_Splice_Rec_840683,Human_Splice_Rec_840757 RMVar_hsa_circ_268487,RMVar_hsa_circ_9980,RMVar_hsa_circ_26523,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 106244 RMVar_ID_106244 Human_SNP_ID_308414772 m1A Human chr7 + 5387914 5387914 5387914 CGCCGCCCGCTGCAGGGCCTCCGGAGTGTGGGAGACGGGCCTGGGCTCGGGAGGCACCCGCAGAG CGCCGCCCGCTGCAGGGCCTCCGGAGTGTGGGGGACGGGCCTGGGCTCGGGAGGCACCCGCAGAG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:5387864..5388047 26863196 MeRIP-seq:(Medium) rs1213861313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106245 RMVar_ID_106245 Human_SNP_ID_308415049 m1A Human chr7 - 5388275 5388275 5388275 CTGAGCATAAATGGAAACCCTTCGAGCTGGGCAACTTCGCCGCCACGCAGATGGCCGTGCTGGCC CTGAGCATAAATGGAAACCCTTCGAGCTGGGCGACTTCGCCGCCACGCAGATGGCCGTGCTGGCC T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5388228..5388548 26863196 MeRIP-seq:(Medium) rs1282855669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7745514,Human_RBP_ID_8911944,Human_RBP_ID_9404244,Human_RBP_ID_17313282,Human_RBP_ID_18101907 RMVar_hsa_circ_268487,RMVar_hsa_circ_9980,RMVar_hsa_circ_26523,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 106246 RMVar_ID_106246 Human_SNP_ID_308416317 m1A Human chr7 + 5390558 5390558 5390558 GGCTGACCCAGCTGGCTGAGGAGGGGGCTCCCACTGCTGGGGGGCTCCAGGTGGTTCAGGTGGAG GGCTGACCCAGCTGGCTGAGGAGGGGGCTCCCGCTGCTGGGGGGCTCCAGGTGGTTCAGGTGGAG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5390441..5390623 26863196 MeRIP-seq:(Medium) rs1341618547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106247 RMVar_ID_106247 Human_SNP_ID_308418662 m1A Human chr7 - 5397207 5397185 5397207 AAGGCGGAAGCCCGGGGCTCAGCAGGGCTTGGAGGCCCTGCTGCCCCGGCTTGGGCCGCATGGAT AAGGCGGAAGCCCGGGGCTCAGCAGGGCTTGG______________________GCCGCATGGAT CCCAAGCCGGGGCAGCAGGGCCT C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5397017..5397216 26863196 MeRIP-seq:(Medium) rs1409599671 Functional Loss DEL dbSNP153 33..54 33 - - - 106248 RMVar_ID_106248 Human_SNP_ID_308418668 m1A Human chr7 - 5397207 5397207 5397207 AAGGCGGAAGCCCGGGGCTCAGCAGGGCTTGGAGGCCCTGCTGCCCCGGCTTGGGCCGCATGGAT AAGGCGGAAGCCCGGGGCTCAGCAGGGCTTGGTGGCCCTGCTGCCCCGGCTTGGGCCGCATGGAT T A TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5397017..5397216 26863196 MeRIP-seq:(Medium) rs1163660349 Functional Loss SNV dbSNP153 33..33 33 - - - 106249 RMVar_ID_106249 Human_SNP_ID_308427500 m1A Human chr7 + 5421076 5421076 5421076 GGCGCGGGGCACTTACCCGGGTGCGGATGGAGATTCAGGCCGGCCATGTACTTCCCGGGCGGCAG GGCGCGGGGCACTTACCCGGGTGCGGATGGAGTTTCAGGCCGGCCATGTACTTCCCGGGCGGCAG A T AC092171.1 Ensembl:ENSG00000188365 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5421069..5421170 32194978 MeRIP-seq:(Medium) rs1158114389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106250 RMVar_ID_106250 Human_SNP_ID_308427641 m1A Human chr7 - 5421356 5421356 5421356 AGCCCCGCTGGCCGCCGCCATGCACGCCGCGGAGCCCCCGCCGCCCGAGGACTCTGGGACTACGC AGCCCCGCTGGCCGCCGCCATGCACGCCGCGGTGCCCCCGCCGCCCGAGGACTCTGGGACTACGC T A TNRC18 Ensembl:ENSG00000182095 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5420127..5422840 26863196 MeRIP-seq:(Medium) rs1224140878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685835,Human_RBP_ID_3862270,Human_RBP_ID_9311764,Human_RBP_ID_16176088,Human_RBP_ID_17427266,Human_RBP_ID_22372336,Human_RBP_ID_22728782,Human_RBP_ID_24438864,Human_RBP_ID_26794339 106251 RMVar_ID_106251 Human_SNP_ID_308428510 m1A Human chr7 + 5423479 5423476 5423479 CGGCTGGGTTCACGGCTCCAGGCTCCGGCGACAACGACTCCGGCGGCGGCCCCGGCTCCCGGCGC CGGCTGGGTTCACGGCTCCAGGCTCCGGCG___ACGACTCCGGCGGCGGCCCCGGCTCCCGGCGC GACA G RF00017-4486,RF00017-4498 RNACentral:URS000090F764,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:5423463..5423551 26863410 MeRIP-seq:(Medium) rs953977965 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106252 RMVar_ID_106252 Human_SNP_ID_308431935 m1A Human chr7 + 5431580 5431577 5431581 TCACACACAGACACACACACACACACACACACAGAGTCACCTCCCCCCACCTTTTTTTCCTTTTT TCACACACAGACACACACACACACACACAC____AGTCACCTCCCCCCACCTTTTTTTCCTTTTT CACAG C RF00017-4486,RF00017-4498 RNACentral:URS000090F764,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5431576..5431703 26863196 MeRIP-seq:(Medium) rs1052967132 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106253 RMVar_ID_106253 Human_SNP_ID_308431936 m1A Human chr7 + 5431580 5431579 5431581 TCACACACAGACACACACACACACACACACACAGAGTCACCTCCCCCCACCTTTTTTTCCTTTTT TCACACACAGACACACACACACACACACACAC__AGTCACCTCCCCCCACCTTTTTTTCCTTTTT CAG C RF00017-4486,RF00017-4498 RNACentral:URS000090F764,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5431576..5431703 26863196 MeRIP-seq:(Medium) rs764386496 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106254 RMVar_ID_106254 Human_SNP_ID_308438185 m1A Human chr7 - 5450908 5450908 5450908 CCATCCCAGCCTTGCTGGGGGCTGAGAGGCCCAGCCTGGGTTGCTATGGTGATGGGATGCGTGGC CCATCCCAGCCTTGCTGGGGGCTGAGAGGCCCCGCCTGGGTTGCTATGGTGATGGGATGCGTGGC T G FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5450906..5451139 26863196 MeRIP-seq:(Medium) rs1024740226 Functional Loss SNV dbSNP153 33..33 33 - - - 106255 RMVar_ID_106255 Human_SNP_ID_308438710 m1A Human chr7 - 5452614 5452613 5452614 GGCCTGGGGCCTCCCCGGGCTGATGCGTGGCCACTATTTCCAAGGCGTGGCCAGACTGGCCCAAG GGCCTGGGGCCTCCCCGGGCTGATGCGTGGCC_CTATTTCCAAGGCGTGGCCAGACTGGCCCAAG GT G FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5452612..5452859 26863196 MeRIP-seq:(Medium) rs1419415778 Functional Loss DEL dbSNP153 33..33 33 - - - 106256 RMVar_ID_106256 Human_SNP_ID_308453227 m1A Human chr7 - 5496362 5496362 5496362 GAGACCGAGCAGAGGCTGTCAGCAAGGGAGGCACTGGCCGGAGGGAGGGGGTGTTCCGGAAGCAA GAGACCGAGCAGAGGCTGTCAGCAAGGGAGGCCCTGGCCGGAGGGAGGGGGTGTTCCGGAAGCAA T G FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5496312..5496439 26863196 MeRIP-seq:(Medium) rs188919779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5327783 RMVar_hsa_circ_277673,RMVar_hsa_circ_243501 106257 RMVar_ID_106257 Human_SNP_ID_308454155 m1A Human chr7 - 5499278 5499278 5499278 GGTGGGAGGGAGTAGGGAAGATGGGGCAGACAAGGAAGGTGGGCAACAGTGCCGAGGGGTTTCAC GGTGGGAGGGAGTAGGGAAGATGGGGCAGACAGGGAAGGTGGGCAACAGTGCCGAGGGGTTTCAC T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5499070..5499428 26863196 MeRIP-seq:(Medium) rs528932655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9439659,Human_RBP_ID_18959108,Human_RBP_ID_26550348 RMVar_hsa_circ_277673,RMVar_hsa_circ_243501 106258 RMVar_ID_106258 Human_SNP_ID_308454875 m1A Human chr7 - 5501082 5501082 5501082 GCGCCACCTGAACCTCTCGGCCGCCCACCACCACAGCTCGGAGGGCCTGGGCCGCCACCTCTGCC GCGCCACCTGAACCTCTCGGCCGCCCACCACCCCAGCTCGGAGGGCCTGGGCCGCCACCTCTGCC T G FBXL18 Ensembl:ENSG00000155034 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5501033..5501104 26863196 MeRIP-seq:(Medium) rs1329390704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9337008,Human_RBP_ID_22110605,Human_RBP_ID_27532570 RMVar_hsa_circ_28891,RMVar_hsa_circ_277673,RMVar_hsa_circ_243501,RMVar_hsa_circ_351444 106259 RMVar_ID_106259 Human_SNP_ID_308459183 m1A Human chr7 - 5513747 5513747 5513747 GTCTCGGTTGAGCGGTGGACGCGCCGGCTTCGAGCATCCCTAGCCGGGCAGGTGGGAGGCACGGG GTCTCGGTTGAGCGGTGGACGCGCCGGCTTCGCGCATCCCTAGCCGGGCAGGTGGGAGGCACGGG T G FBXL18 Ensembl:ENSG00000155034 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5513658..5513766 26863196 MeRIP-seq:(Medium) rs1429932243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956143 Human_Splice_Rec_840779,Human_Splice_Rec_840791,Human_Splice_Rec_840799 106260 RMVar_ID_106260 Human_SNP_ID_308459185 m1A Human chr7 + 5513750 5513750 5513750 GTGCCTCCCACCTGCCCGGCTAGGGATGCTCGAAGCCGGCGCGTCCACCGCTCAACCGAGACCCC GTGCCTCCCACCTGCCCGGCTAGGGATGCTCGTAGCCGGCGCGTCCACCGCTCAACCGAGACCCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5513658..5513762 26863196 MeRIP-seq:(Medium) rs1385061860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106261 RMVar_ID_106261 Human_SNP_ID_308463802 m1A Human chr7 + 5527379 5527379 5527379 AAAATTTTGCATTACATAATTTACACGAAAGCAATGCTATCACCTCCCCTGTGTGGACTTGGGAG AAAATTTTGCATTACATAATTTACACGAAAGCCATGCTATCACCTCCCCTGTGTGGACTTGGGAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:5527290..5527388 26863410 MeRIP-seq:(Medium) rs11546923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106262 RMVar_ID_106262 Human_SNP_ID_308463902 m1A Human chr7 + 5527592 5527592 5527592 GATGCTCGCTCCAACCGACTGCTGTCACCTTCACCGTTCCAGTTTTTAAATCCTGAGTCAAGCCA GATGCTCGCTCCAACCGACTGCTGTCACCTTCCCCGTTCCAGTTTTTAAATCCTGAGTCAAGCCA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:5527491..5527613 26863410 MeRIP-seq:(Medium) rs887488041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106263 RMVar_ID_106263 Human_SNP_ID_308464339 m1A Human chr7 - 5528430 5528430 5528430 AATCGTGCGTGACATTAAGGAGAAGCTGTGCTACGTCGCCCTGGACTTCGAGCAAGAGATGGCCA AATCGTGCGTGACATTAAGGAGAAGCTGTGCTCCGTCGCCCTGGACTTCGAGCAAGAGATGGCCA T G ACTB Ensembl:ENSG00000075624 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5528287..5528712 26863196 MeRIP-seq:(Medium) rs11546898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_956080,Human_RBP_ID_1052530,Human_RBP_ID_1687648,Human_RBP_ID_2044280,Human_RBP_ID_3848741,Human_RBP_ID_5622994,Human_RBP_ID_7746249,Human_RBP_ID_8669076,Human_RBP_ID_8911987,Human_RBP_ID_9211881,Human_RBP_ID_16179188,Human_RBP_ID_17313304,Human_RBP_ID_17425852,Human_RBP_ID_17541769,Human_RBP_ID_18102106,Human_RBP_ID_21396870,Human_RBP_ID_22463879,Human_RBP_ID_24219600,Human_RBP_ID_24516817,Human_RBP_ID_27114844,Human_RBP_ID_27161609,Human_RBP_ID_27358638,Human_RBP_ID_27532638 RMVar_hsa_circ_77074,RMVar_hsa_circ_110714,RMVar_hsa_circ_126855,RMVar_hsa_circ_119696,RMVar_hsa_circ_91911,RMVar_hsa_circ_243503,RMVar_hsa_circ_243505,RMVar_hsa_circ_243506,RMVar_hsa_circ_243504,RMVar_hsa_circ_105019,RMVar_hsa_circ_88728,RMVar_hsa_circ_47316,RMVar_hsa_circ_123677,RMVar_hsa_circ_243510,RMVar_hsa_circ_243511,RMVar_hsa_circ_243512,RMVar_hsa_circ_243514,RMVar_hsa_circ_94753,RMVar_hsa_circ_243513 106264 RMVar_ID_106264 Human_SNP_ID_308464936 m1A Human chr7 + 5529583 5529583 5529583 CCCACGATGGAGGGGAAGACGGCCCGGGGGGCATCGTCGCCCGCGAAGCCGGCCTTGCACATGCC CCCACGATGGAGGGGAAGACGGCCCGGGGGGCGTCGTCGCCCGCGAAGCCGGCCTTGCACATGCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:5529380..5529727 26863196 MeRIP-seq:(Medium) rs773087350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106265 RMVar_ID_106265 Human_SNP_ID_308464950 m1A Human chr7 - 5529623 5529623 5529623 GGATGATGATATCGCCGCGCTCGTCGTCGACAACGGCTCCGGCATGTGCAAGGCCGGCTTCGCGG GGATGATGATATCGCCGCGCTCGTCGTCGACACCGGCTCCGGCATGTGCAAGGCCGGCTTCGCGG T G ACTB Ensembl:ENSG00000075624 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5529101..5529773 26863196 MeRIP-seq:(Medium) rs774758441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686016,Human_RBP_ID_1052537,Human_RBP_ID_1687666,Human_RBP_ID_2044288,Human_RBP_ID_3848754,Human_RBP_ID_4945009,Human_RBP_ID_5219392,Human_RBP_ID_5429647,Human_RBP_ID_5513496,Human_RBP_ID_7746281,Human_RBP_ID_8669093,Human_RBP_ID_8911997,Human_RBP_ID_9337009,Human_RBP_ID_16179247,Human_RBP_ID_17541777,Human_RBP_ID_18211597,Human_RBP_ID_18883967,Human_RBP_ID_22463008,Human_RBP_ID_22534238,Human_RBP_ID_24219618,Human_RBP_ID_24438466,Human_RBP_ID_26552364,Human_RBP_ID_26830149,Human_RBP_ID_27114857,Human_RBP_ID_27161799,Human_RBP_ID_27532666 Human_Splice_Rec_840812,Human_Splice_Rec_840813,Human_Splice_Rec_840826,Human_Splice_Rec_840827,Human_Splice_Rec_840838,Human_Splice_Rec_840839,Human_Splice_Rec_840847,Human_Splice_Rec_840862,Human_Splice_Rec_840863,Human_Splice_Rec_840874,Human_Splice_Rec_840877,Human_Splice_Rec_840882,Human_Splice_Rec_840883,Human_Splice_Rec_840889,Human_Splice_Rec_840896,Human_Splice_Rec_840897,Human_Splice_Rec_840902,Human_Splice_Rec_840904,Human_Splice_Rec_840905,Human_Splice_Rec_840908,Human_Splice_Rec_840909,Human_Splice_Rec_840914,Human_Splice_Rec_840915 RMVar_hsa_circ_110714,RMVar_hsa_circ_126855,RMVar_hsa_circ_243503,RMVar_hsa_circ_243504,RMVar_hsa_circ_105019,RMVar_hsa_circ_88728,RMVar_hsa_circ_123677,RMVar_hsa_circ_243511,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243514,RMVar_hsa_circ_373642,RMVar_hsa_circ_243516,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 106266 RMVar_ID_106266 Human_SNP_ID_308464977 m1A Human chr7 + 5529662 5529662 5529662 CGACGAGCGCGGCGATATCATCATCCATGGTGAGCTGCGAGAATAGCCGGGCGCGCTGTGAGCCG CGACGAGCGCGGCGATATCATCATCCATGGTGGGCTGCGAGAATAGCCGGGCGCGCTGTGAGCCG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control chr7:5529576..5529716;chr7:5529601..5529729;chr7:5529576..5529722;chr7:5529576..5529729 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs1343972830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106267 RMVar_ID_106267 Human_SNP_ID_308465540 m1A Human chr7 - 5530476 5530466 5530476 CGACCGGGGCAGGCGGCTCACGGCCCGGCCGCAGGCGGCCGCGGCCCCTTCGCCCGTGCAGAGCC CGACCGGGGCAGGCGGCTCACGGCCCGGCCGC__________GGCCCCTTCGCCCGTGCAGAGCC CGCGGCCGCCT C ACTB Ensembl:ENSG00000075624 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr7:5530461..5530625;chr7:5530465..5530602 26863410 MeRIP-seq:(Medium) rs1367007221 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_110714,RMVar_hsa_circ_243503,RMVar_hsa_circ_105019,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 106268 RMVar_ID_106268 Human_SNP_ID_308465571 m1A Human chr7 - 5530506 5530506 5530506 CACACCCGCCGCCAGGTAAGCCCGGCCAGCCGACCGGGGCAGGCGGCTCACGGCCCGGCCGCAGG CACACCCGCCGCCAGGTAAGCCCGGCCAGCCGGCCGGGGCAGGCGGCTCACGGCCCGGCCGCAGG T C ACTB Ensembl:ENSG00000075624 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:5530501..5530600 32194978 MeRIP-seq:(Medium) rs981001949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5221231 RMVar_hsa_circ_110714,RMVar_hsa_circ_243503,RMVar_hsa_circ_105019,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 106269 RMVar_ID_106269 Human_SNP_ID_308465622 m1A Human chr7 - 5530570 5530570 5530570 CACCGCCGAGACCGCGTCCGCCCCGCGAGCACAGAGCCTCGCCTTTGCCGATCCGCCGCCCGTCC CACCGCCGAGACCGCGTCCGCCCCGCGAGCACGGAGCCTCGCCTTTGCCGATCCGCCGCCCGTCC T C ACTB Ensembl:ENSG00000075624 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:5529920..5530625;chr7:5529801..5530625;chr7:5530246..5530625 26863196 MeRIP-seq:(Medium) rs1046070734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83086,Human_RBP_ID_253038,Human_RBP_ID_686018,Human_RBP_ID_792852,Human_RBP_ID_1687671,Human_RBP_ID_2044291,Human_RBP_ID_4964152,Human_RBP_ID_7746290,Human_RBP_ID_8669099,Human_RBP_ID_9337019,Human_RBP_ID_16179253,Human_RBP_ID_18883970,Human_RBP_ID_22534240,Human_RBP_ID_23077306,Human_RBP_ID_24219620,Human_RBP_ID_24516840,Human_RBP_ID_27532673 Human_Splice_Rec_840811,Human_Splice_Rec_840825,Human_Splice_Rec_840837,Human_Splice_Rec_840845,Human_Splice_Rec_840855,Human_Splice_Rec_840861,Human_Splice_Rec_840869,Human_Splice_Rec_840873,Human_Splice_Rec_840887,Human_Splice_Rec_840895,Human_Splice_Rec_840901 Human_miRNA_ID_3068560 RMVar_hsa_circ_110714,RMVar_hsa_circ_243503,RMVar_hsa_circ_105019,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 106270 RMVar_ID_106270 Human_SNP_ID_308465625 m1A Human chr7 - 5530572 5530572 5530572 ACCACCGCCGAGACCGCGTCCGCCCCGCGAGCACAGAGCCTCGCCTTTGCCGATCCGCCGCCCGT ACCACCGCCGAGACCGCGTCCGCCCCGCGAGCGCAGAGCCTCGCCTTTGCCGATCCGCCGCCCGT T C ACTB Ensembl:ENSG00000075624 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5529901..5530625 26863196 MeRIP-seq:(Medium) rs1386877155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_83086,Human_RBP_ID_253038,Human_RBP_ID_686018,Human_RBP_ID_792852,Human_RBP_ID_1687671,Human_RBP_ID_2044291,Human_RBP_ID_4964152,Human_RBP_ID_7746290,Human_RBP_ID_9337019,Human_RBP_ID_18883970,Human_RBP_ID_22324203,Human_RBP_ID_22534240,Human_RBP_ID_24219620,Human_RBP_ID_24516840,Human_RBP_ID_27532673 Human_Splice_Rec_840811,Human_Splice_Rec_840825,Human_Splice_Rec_840837,Human_Splice_Rec_840845,Human_Splice_Rec_840855,Human_Splice_Rec_840861,Human_Splice_Rec_840869,Human_Splice_Rec_840873,Human_Splice_Rec_840887,Human_Splice_Rec_840895,Human_Splice_Rec_840901 Human_miRNA_ID_3068560 RMVar_hsa_circ_110714,RMVar_hsa_circ_243503,RMVar_hsa_circ_105019,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 106271 RMVar_ID_106271 Human_SNP_ID_308488101 m1A Human chr7 + 5593402 5593402 5593402 ACAGCGTCACCCGTAAGCGCTACGCGCACCTGAGCGCGCGGCCGGCCGACGAGATCGCCGTGGAC ACAGCGTCACCCGTAAGCGCTACGCGCACCTGGGCGCGCGGCCGGCCGACGAGATCGCCGTGGAC A G FSCN1 Ensembl:ENSG00000075618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5593364..5593519 26863196 MeRIP-seq:(Medium) rs755866918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173885,Human_RBP_ID_792821,Human_RBP_ID_8914901,Human_RBP_ID_18195923,Human_RBP_ID_22110613,Human_RBP_ID_26830152 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106272 RMVar_ID_106272 Human_SNP_ID_308488119 m1A Human chr7 + 5593433 5593433 5593433 GAGCGCGCGGCCGGCCGACGAGATCGCCGTGGACCGCGACGTGCCCTGGGGCGTCGACTCGCTCA GAGCGCGCGGCCGGCCGACGAGATCGCCGTGGGCCGCGACGTGCCCTGGGGCGTCGACTCGCTCA A G FSCN1 Ensembl:ENSG00000075618 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5593383..5593507 26863196 MeRIP-seq:(Medium) rs1342392528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173885,Human_RBP_ID_686271,Human_RBP_ID_8912036,Human_RBP_ID_9311213,Human_RBP_ID_22110613,Human_RBP_ID_22463890,Human_RBP_ID_27532756 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106273 RMVar_ID_106273 Human_SNP_ID_308491371 m1A Human chr7 + 5603333 5603333 5603333 ACCTTCCAGCTGGAGATCGACCGCGACACCAAAAAGTGTGCCTTCCGTACCCACACGGGCAAGTA ACCTTCCAGCTGGAGATCGACCGCGACACCAAGAAGTGTGCCTTCCGTACCCACACGGGCAAGTA A G FSCN1 Ensembl:ENSG00000075618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:5603216..5603630;chr7:5603235..5603363 26863196 MeRIP-seq:(Medium) rs771337278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1399077,Human_RBP_ID_24219895,Human_RBP_ID_27161630,Human_RBP_ID_27532759 Human_Splice_Rec_840920,Human_Splice_Rec_840921,Human_Splice_Rec_840926,Human_Splice_Rec_840927,Human_Splice_Rec_840931,Human_Splice_Rec_840936,Human_Splice_Rec_840937,Human_Splice_Rec_840941 Human_miRNA_ID_1963915,Human_miRNA_ID_1963916,Human_miRNA_ID_2763364,Human_miRNA_ID_2763365,Human_miRNA_ID_2931587,Human_miRNA_ID_2931588 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_116777,RMVar_hsa_circ_277176,RMVar_hsa_circ_377061,RMVar_hsa_circ_243519,RMVar_hsa_circ_243520 106274 RMVar_ID_106274 Human_SNP_ID_308491434 m1A Human chr7 - 5603478 5603478 5603478 TAGCAGCTGGCATTCCTGGGGGATGGCGGGACAGGGTCAGGCGGGGTAGCCCAGGCAAGGTGGTG TAGCAGCTGGCATTCCTGGGGGATGGCGGGACGGGGTCAGGCGGGGTAGCCCAGGCAAGGTGGTG T C RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:5603476..5603525 32194978 MeRIP-seq:(Medium) rs201921858 Functional Loss SNV dbSNP153 33..33 33 - - - 106275 RMVar_ID_106275 Human_SNP_ID_308491636 m1A Human chr7 - 5603950 5603950 5603950 AGCTGGAGCGGTTGGCGTCCAGGGTGCCCGTGACCTTGCGGCAGCCGATGAAGCCATGCTCCCCG AGCTGGAGCGGTTGGCGTCCAGGGTGCCCGTGTCCTTGCGGCAGCCGATGAAGCCATGCTCCCCG T A RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:5603851..5604063;chr7:5603854..5604045 26863196 MeRIP-seq:(Medium) rs750033509 Functional Loss SNV dbSNP153 33..33 33 - - - 106276 RMVar_ID_106276 Human_SNP_ID_308492231 m1A Human chr7 - 5605626 5605626 5605626 GCGGAGGGGAGAGTGGGGAGTCCATAGGGGCGACAGGTGGGGGCACCGTTTTCTCTGGGGTTTCC GCGGAGGGGAGAGTGGGGAGTCCATAGGGGCGTCAGGTGGGGGCACCGTTTTCTCTGGGGTTTCC T A RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5605576..5605675 26863196 MeRIP-seq:(Medium) rs1406524905 Functional Loss SNV dbSNP153 33..33 33 - - - 106277 RMVar_ID_106277 Human_SNP_ID_308492435 m1A Human chr7 - 5606422 5606422 5606422 GCTTCATCCACCCGGGAGGCCCAGGGAGCACCAATCACAGCAGGGGCTCTGGCCCAGGTGTCGGC GCTTCATCCACCCGGGAGGCCCAGGGAGCACCCATCACAGCAGGGGCTCTGGCCCAGGTGTCGGC T G RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5606373..5606589 26863196 MeRIP-seq:(Medium) rs1328207019 Functional Loss SNV dbSNP153 33..33 33 - - - 106278 RMVar_ID_106278 Human_SNP_ID_308492459 m1A Human chr7 - 5606504 5606504 5606504 GATGCATGTTGGGGACGGGGGAGGCTGGCAGCAGGGGGGCCCCGGCGGCTCACCCCAGGGCTCCC GATGCATGTTGGGGACGGGGGAGGCTGGCAGCTGGGGGGCCCCGGCGGCTCACCCCAGGGCTCCC T A RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr7:5606301..5606599;chr7:5606273..5606625;chr7:5606281..5606625;chr7:5606338..5606590;chr7:5606220..5606598;chr7:5606275..5606550 26863196 MeRIP-seq:(Medium) rs1335413830 Functional Loss SNV dbSNP153 33..33 33 - - - 106279 RMVar_ID_106279 Human_SNP_ID_308498283 m1A Human chr7 - 5622879 5622879 5622879 GGAGCACAACCTGCCCATGCACTTTGGCCCCCAGCCGCGGCATCGCTTCTGATGGCCCCGAATCC GGAGCACAACCTGCCCATGCACTTTGGCCCCCCGCCGCGGCATCGCTTCTGATGGCCCCGAATCC T G RNF216 Ensembl:ENSG00000011275 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:5622831..5623027 26863196 MeRIP-seq:(Medium) rs970746521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5533429 106280 RMVar_ID_106280 Human_SNP_ID_308498331 m1A Human chr7 + 5622969 5622969 5622969 CATAGTTGACCCGCACGTTGGGCAGAGGGGGCACGTACGGGGCTGGGATAGGCCCCATGTTGAGT CATAGTTGACCCGCACGTTGGGCAGAGGGGGCGCGTACGGGGCTGGGATAGGCCCCATGTTGAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5622918..5623119 26863196 MeRIP-seq:(Medium) rs1449103875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106281 RMVar_ID_106281 Human_SNP_ID_308516988 m1A Human chr7 - 5680821 5680821 5680821 GTAAAGAGAAAGGAGGAATTGGGTTTTGTTGCATGAGCAGCCAGTGGGTGGCTGTGTCCTTCAGG GTAAAGAGAAAGGAGGAATTGGGTTTTGTTGCGTGAGCAGCCAGTGGGTGGCTGTGTCCTTCAGG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5680819..5681078 26863196 MeRIP-seq:(Medium) rs1371363697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3095436,Human_RBP_ID_16181794,Human_RBP_ID_24219939 RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_82528,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_243530 106282 RMVar_ID_106282 Human_SNP_ID_308620033 m1A Human chr7 + 5987404 5987404 5987405 TGTCAGAGATGGCACCTGAAGTGCTAGAAGACAGCATACCCCTTTTCTGTCCTAGAGGGCTCCTT TGTCAGAGATGGCACCTGAAGTGCTAGAAGACGACATACCCCTTTTCTGTCCTAGAGGGCTCCTT AG GA RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:5987274..5987416 26863196 MeRIP-seq:(Medium) rs587778615 Functional Loss MNV dbSNP153 33..34 33 - - - Clinvar_Rec_680 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106283 RMVar_ID_106283 Human_SNP_ID_308620034 m1A Human chr7 + 5987404 5987404 5987404 TGTCAGAGATGGCACCTGAAGTGCTAGAAGACAGCATACCCCTTTTCTGTCCTAGAGGGCTCCTT TGTCAGAGATGGCACCTGAAGTGCTAGAAGACGGCATACCCCTTTTCTGTCCTAGAGGGCTCCTT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:5987274..5987416 26863196 MeRIP-seq:(Medium) rs772659239 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_681 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106284 RMVar_ID_106284 Human_SNP_ID_308627689 m1A Human chr7 - 6008908 6008908 6008908 ACGGCATTCCAACCTCCCTGGAAATGGGGGGAACATGGCCGAGGCGCGTGGCGAGGCAGCCCCCT ACGGCATTCCAACCTCCCTGGAAATGGGGGGAGCATGGCCGAGGCGCGTGGCGAGGCAGCCCCCT T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:6008903..6009066 26863196 MeRIP-seq:(Medium) rs1440457966 Functional Loss SNV dbSNP153 33..33 33 - - - 106285 RMVar_ID_106285 Human_SNP_ID_308627974 m1A Human chr7 - 6009327 6009327 6009327 GAACCAAAGCAAAAGGGGGTAGCGCGTGCCAAAGGCCAACGCTCAGAAACCGTCAGAGGTCACGA GAACCAAAGCAAAAGGGGGTAGCGCGTGCCAATGGCCAACGCTCAGAAACCGTCAGAGGTCACGA T A RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6009276..6009412 26863196 MeRIP-seq:(Medium) rs1458102513 Functional Loss SNV dbSNP153 33..33 33 - - - 106286 RMVar_ID_106286 Human_SNP_ID_308627979 m1A Human chr7 + 6009333 6009333 6009333 CCTCTGACGGTTTCTGAGCGTTGGCCTTTGGCACGCGCTACCCCCTTTTGCTTTGGTTCTGCCAT CCTCTGACGGTTTCTGAGCGTTGGCCTTTGGCTCGCGCTACCCCCTTTTGCTTTGGTTCTGCCAT A T AIMP2 Ensembl:ENSG00000106305 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6009251..6009445 26863196 MeRIP-seq:(Medium) rs1307337248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686345,Human_RBP_ID_4955643,Human_RBP_ID_16183176 Human_Splice_Rec_841583 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 106287 RMVar_ID_106287 Human_SNP_ID_308628056 m1A Human chr7 + 6009448 6009448 6009448 TGGAGCTTCCCACCTGCATGTACCGGCTCCCCAACGTGCACGGCAGGAGCTACGGCCCAGCGCCG TGGAGCTTCCCACCTGCATGTACCGGCTCCCCCACGTGCACGGCAGGAGCTACGGCCCAGCGCCG A C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:6009301..6009500 32194978 MeRIP-seq:(Medium) rs1381117753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4945694,Human_RBP_ID_18102310,Human_RBP_ID_27358810 Human_Splice_Rec_841591,Human_Splice_Rec_841597,Human_Splice_Rec_841601 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 106288 RMVar_ID_106288 Human_SNP_ID_308628057 m1A Human chr7 + 6009448 6009448 6009448 TGGAGCTTCCCACCTGCATGTACCGGCTCCCCAACGTGCACGGCAGGAGCTACGGCCCAGCGCCG TGGAGCTTCCCACCTGCATGTACCGGCTCCCCGACGTGCACGGCAGGAGCTACGGCCCAGCGCCG A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:6009301..6009500 32194978 MeRIP-seq:(Medium) rs1381117753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4945694,Human_RBP_ID_18102310,Human_RBP_ID_27358810 Human_Splice_Rec_841591,Human_Splice_Rec_841597,Human_Splice_Rec_841601 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 106289 RMVar_ID_106289 Human_SNP_ID_308633304 m1A Human chr7 - 6024016 6024016 6024016 CAGCTCAGATCTCTTTCCTGCCTTTGCCCTGCACTGTTCCCCGGTACTTCCTCCTTTATTGTAGC CAGCTCAGATCTCTTTCCTGCCTTTGCCCTGCCCTGTTCCCCGGTACTTCCTCCTTTATTGTAGC T G EIF2AK1 Ensembl:ENSG00000086232 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6023966..6024086 26863196 MeRIP-seq:(Medium) rs974700848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686371,Human_RBP_ID_3849079,Human_RBP_ID_17316001,Human_RBP_ID_17426862,Human_RBP_ID_17543159,Human_RBP_ID_18959935 Human_miRNA_ID_229545,Human_miRNA_ID_329334,Human_miRNA_ID_333360,Human_miRNA_ID_350407,Human_miRNA_ID_592389,Human_miRNA_ID_762551,Human_miRNA_ID_767452,Human_miRNA_ID_1327032 106290 RMVar_ID_106290 Human_SNP_ID_308633319 m1A Human chr7 + 6024054 6024054 6024054 GCAAAGGCAGGAAAGAGATCTGAGCTGCCTGGAGATCATCTGGGGTGCGGAGTACAAAGCTTTGC GCAAAGGCAGGAAAGAGATCTGAGCTGCCTGGCGATCATCTGGGGTGCGGAGTACAAAGCTTTGC A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr7:6023972..6024176;chr7:6024003..6024158 26863196 MeRIP-seq:(Medium) rs1360926041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106291 RMVar_ID_106291 Human_SNP_ID_308633332 m1A Human chr7 - 6024094 6024094 6024094 CTCCACCTTCAGTTTAGCGTCATTCCAAAACCACACCCTTGCAAAGCTTTGTACTCCGCACCCCA CTCCACCTTCAGTTTAGCGTCATTCCAAAACCGCACCCTTGCAAAGCTTTGTACTCCGCACCCCA T C EIF2AK1 Ensembl:ENSG00000086232 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:6024048..6024180 26863196 MeRIP-seq:(Medium) rs538382623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86701,Human_RBP_ID_686371,Human_RBP_ID_7747226,Human_RBP_ID_17313355,Human_RBP_ID_17426865,Human_RBP_ID_17541841,Human_RBP_ID_18959937,Human_RBP_ID_21561934,Human_RBP_ID_24439965,Human_RBP_ID_24516911,Human_RBP_ID_26547888 106292 RMVar_ID_106292 Human_SNP_ID_308633350 m1A Human chr7 + 6024127 6024127 6024127 GGTTTTGGAATGACGCTAAACTGAAGGTGGAGAGAACAGATAAAAAGGTTGGAAGTTGCACACTG GGTTTTGGAATGACGCTAAACTGAAGGTGGAGGGAACAGATAAAAAGGTTGGAAGTTGCACACTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:6024076..6024150 26863196 MeRIP-seq:(Medium) rs1359146059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106293 RMVar_ID_106293 Human_SNP_ID_308633375 m1A Human chr7 + 6024201 6024201 6024201 AAGAAGTTGAGCTTTTATCTTAGAGGCAGCAGAAGGTTTGGAGCCAAGGAATGAAATGATGAGGC AAGAAGTTGAGCTTTTATCTTAGAGGCAGCAGCAGGTTTGGAGCCAAGGAATGAAATGATGAGGC A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:6024176..6024200 26863196 MeRIP-seq:(Medium) rs1315860145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106294 RMVar_ID_106294 Human_SNP_ID_308637621 m1A Human chr7 + 6038612 6038612 6038612 TCCCGGCCCCGCTTGTTTCTCTCGACTATCCAATCCCACAGCGAGAGCTCACACAGCTGCATCTG TCCCGGCCCCGCTTGTTTCTCTCGACTATCCAGTCCCACAGCGAGAGCTCACACAGCTGCATCTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6038516..6038631 26863196 MeRIP-seq:(Medium) rs766304507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106295 RMVar_ID_106295 Human_SNP_ID_308637622 m1A Human chr7 + 6038612 6038612 6038612 TCCCGGCCCCGCTTGTTTCTCTCGACTATCCAATCCCACAGCGAGAGCTCACACAGCTGCATCTG TCCCGGCCCCGCTTGTTTCTCTCGACTATCCATTCCCACAGCGAGAGCTCACACAGCTGCATCTG A T RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6038516..6038631 26863196 MeRIP-seq:(Medium) rs766304507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106296 RMVar_ID_106296 Human_SNP_ID_308642653 m1A Human chr7 + 6054677 6054677 6054677 GGAAGGTTGGCTGTTGTAGGGGTTCTTTTAACACCTGGATTTCTGCTGGAACATCAGATTCTAAA GGAAGGTTGGCTGTTGTAGGGGTTCTTTTAACCCCTGGATTTCTGCTGGAACATCAGATTCTAAA A C RF00017-4575,lnc-ANKRD61-1,lnc-ANKRD61-1:2 RNACentral:URS0000918622,RNACentral:URS00008B2C0D,RNACentral:URS00008B3EE3 SRP RNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:6054626..6054725 26863196 MeRIP-seq:(Medium) rs1173141543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106297 RMVar_ID_106297 Human_SNP_ID_308642663 m1A Human chr7 - 6054706 6054706 6054706 TTAATTTAAAAATATTTTCCTTTTTAATTTTTAGAATCTGATGTTCCAGCAGAAATCCAGGTGTT TTAATTTAAAAATATTTTCCTTTTTAATTTTTGGAATCTGATGTTCCAGCAGAAATCCAGGTGTT T C EIF2AK1 Ensembl:ENSG00000086232 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6054676..6054725 26863196 MeRIP-seq:(Medium) rs768298421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4964402,Human_RBP_ID_7747318,Human_RBP_ID_22686685,Human_RBP_ID_27358854 106298 RMVar_ID_106298 Human_SNP_ID_308644413 m1A Human chr7 + 6059122 6059122 6059122 CCGCGCGCGGGCCGCAGCCCAGCCCGCCGGCCAGCCCAGCACTGCCACACTCCGATGCTGCAGCT CCGCGCGCGGGCCGCAGCCCAGCCCGCCGGCCGGCCCAGCACTGCCACACTCCGATGCTGCAGCT A G RF00017-4575,lnc-ANKRD61-1,lnc-ANKRD61-1:2 RNACentral:URS0000918622,RNACentral:URS00008B2C0D,RNACentral:URS00008B3EE3 SRP RNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:6058914..6059200;chr7:6058919..6059200 26863196 MeRIP-seq:(Medium) rs943402384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106299 RMVar_ID_106299 Human_SNP_ID_308652059 m1A Human chr7 - 6081376 6081376 6081376 GCGGGGCCGGGGCTGTGGCTGCGCCGCCCGCCATCTACCTCCCCGCGGCGGCCCGGCCCCCGGTA GCGGGGCCGGGGCTGTGGCTGCGCCGCCCGCCGTCTACCTCCCCGCGGCGGCCCGGCCCCCGGTA T C lnc-EIF2AK1-4,lnc-EIF2AK1-4:2,RF00017-2064 RNACentral:URS0000D5A578,RNACentral:URS0000D5CBC9,RNACentral:URS000098196C lincRNA,lincRNA,SRP RNA exon,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6081339..6081492 26863196 MeRIP-seq:(Medium) rs576984100 Functional Loss SNV dbSNP153 33..33 33 - - - 106300 RMVar_ID_106300 Human_SNP_ID_308661540 m1A Human chr7 + 6109138 6109138 6109138 GGTGATGTCAAGGAAAGTGTCCCAGAGAAAGTAAAGTCTAAACTGAGAAGTGGAAGTGTGAACTG GGTGATGTCAAGGAAAGTGTCCCAGAGAAAGTGAAGTCTAAACTGAGAAGTGGAAGTGTGAACTG A G USP42 Ensembl:ENSG00000106346 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6109132..6109331 26863196 MeRIP-seq:(Medium) rs557619179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_94958,RMVar_hsa_circ_243600 106301 RMVar_ID_106301 Human_SNP_ID_308676777 m1A Human chr7 + 6153845 6153845 6153845 CAGCCCCGCCGCCGAATCCCTGGAGGAGCCAGATGCGGCCGCCGGCCTCAGCAGCACCAAGAAGG CAGCCCCGCCGCCGAATCCCTGGAGGAGCCAGGTGCGGCCGCCGGCCTCAGCAGCACCAAGAAGG A G USP42 Ensembl:ENSG00000106346 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6153794..6153942 26863196 MeRIP-seq:(Medium) rs1350933600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9404261 Human_Splice_Rec_841738,Human_Splice_Rec_841794,Human_Splice_Rec_841850,Human_Splice_Rec_841880 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_94958,RMVar_hsa_circ_243600,RMVar_hsa_circ_127757,RMVar_hsa_circ_243616,RMVar_hsa_circ_70751,RMVar_hsa_circ_362796,RMVar_hsa_circ_308741,RMVar_hsa_circ_346783,RMVar_hsa_circ_243621 106302 RMVar_ID_106302 Human_SNP_ID_308681251 m1A Human chr7 + 6164220 6164208 6164221 GCTGCCCCCCGGGGCTTGTCTGACAGCCTGACAGGGCAGGGCTGCACGCTGCCCCCGTGCCGGTG GCTGCCCCCCGGGGCTTGTCT_____________GGCAGGGCTGCACGCTGCCCCCGTGCCGGTG TGACAGCCTGACAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6164173..6164259 26863196 MeRIP-seq:(Medium) rs999438917 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106303 RMVar_ID_106303 Human_SNP_ID_308681264 m1A Human chr7 - 6164237 6164237 6164237 AAGGGGAGGGCTGGGGGCACCGGCACGGGGGCAGCGTGCAGCCCTGCCCTGTCAGGCTGTCAGAC AAGGGGAGGGCTGGGGGCACCGGCACGGGGGCCGCGTGCAGCCCTGCCCTGTCAGGCTGTCAGAC T G CYTH3 Ensembl:ENSG00000008256 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6164186..6164260 26863196 MeRIP-seq:(Medium) rs1362539237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26551172 Human_miRNA_ID_462667,Human_miRNA_ID_929453,Human_miRNA_ID_2151001,Human_miRNA_ID_2419487 RMVar_hsa_circ_94115,RMVar_hsa_circ_243622 106304 RMVar_ID_106304 Human_SNP_ID_308682356 m1A Human chr7 - 6166925 6166925 6166925 TTGCCCAGACCAGGGTCTAGACAGACCCTTTAACAGGTAGGCTGGTGGGACACTGATGAGACTGG TTGCCCAGACCAGGGTCTAGACAGACCCTTTACCAGGTAGGCTGGTGGGACACTGATGAGACTGG T G CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6166918..6167181 26863196 MeRIP-seq:(Medium) rs920516924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5328380,Human_RBP_ID_16184282 RMVar_hsa_circ_94115,RMVar_hsa_circ_243622 106305 RMVar_ID_106305 Human_SNP_ID_308684282 m1A Human chr7 - 6172318 6172318 6172318 GTGCAGGCCTGGCGGAGAAGAAGGGGCCTGGTAGAGAGTGGGGCCAGACGTGGCTGGAATCCTGG GTGCAGGCCTGGCGGAGAAGAAGGGGCCTGGTCGAGAGTGGGGCCAGACGTGGCTGGAATCCTGG T G CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6172267..6172398 26863196 MeRIP-seq:(Medium) rs1335305230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5327796,Human_RBP_ID_21992888 RMVar_hsa_circ_94115,RMVar_hsa_circ_44597,RMVar_hsa_circ_243622,RMVar_hsa_circ_243623 106306 RMVar_ID_106306 Human_SNP_ID_308700445 m1A Human chr7 + 6220896 6220896 6220896 CGGGCACCTGTAGTCCCAGCCAATTGGGAGGCAGTGGCAGGAGAATTGCTTGAACACGGGAGGCA CGGGCACCTGTAGTCCCAGCCAATTGGGAGGCTGTGGCAGGAGAATTGCTTGAACACGGGAGGCA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:6220784..6220913 26863196 MeRIP-seq:(Medium) rs1300169770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106307 RMVar_ID_106307 Human_SNP_ID_308713642 m1A Human chr7 - 6260655 6260655 6260655 AGAGAGAAGGAGTGATCGATCAGCTGTGTTGAATGCACTTAGAGACGGCCTAAAATGGGGATGGG AGAGAGAAGGAGTGATCGATCAGCTGTGTTGAGTGCACTTAGAGACGGCCTAAAATGGGGATGGG T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6260653..6260872 26863196 MeRIP-seq:(Medium) rs753677496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16184626 106308 RMVar_ID_106308 Human_SNP_ID_308715479 m1A Human chr7 - 6266654 6266654 6266654 GAAATGCCCTTCGAGGTGCAATCTATAGGGGTAGTGGACCAGACAGAAGGGAAGGCATGGAGCTG GAAATGCCCTTCGAGGTGCAATCTATAGGGGTGGTGGACCAGACAGAAGGGAAGGCATGGAGCTG T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6266652..6266783 26863196 MeRIP-seq:(Medium) rs759932128 Functional Loss SNV dbSNP153 33..33 33 - - - 106309 RMVar_ID_106309 Human_SNP_ID_308717043 m1A Human chr7 + 6271819 6271819 6271819 TGCCTCTGTGCTGGGTGCAGCTCGTGTCTCCCACCCTCGGCTCCACGGAGTTTTTTGCTCAATCT TGCCTCTGTGCTGGGTGCAGCTCGTGTCTCCCCCCCTCGGCTCCACGGAGTTTTTTGCTCAATCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:6271689..6271856 26863196 MeRIP-seq:(Medium) rs1433766788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106310 RMVar_ID_106310 Human_SNP_ID_308717255 m1A Human chr7 - 6272373 6272373 6272373 GCGCGGCGCTGGGCCGGGGTTCGCCGGAGGAGACGGGGTCGGGGGCAGCGGCAGCGGCGTCCGCT GCGCGGCGCTGGGCCGGGGTTCGCCGGAGGAGGCGGGGTCGGGGGCAGCGGCAGCGGCGTCCGCT T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:6272274..6272406 26863196 MeRIP-seq:(Medium) rs1471935379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860460,Human_RBP_ID_5090497,Human_RBP_ID_5402030,Human_RBP_ID_8150441,Human_RBP_ID_8218250,Human_RBP_ID_9337034,Human_RBP_ID_9439215 106311 RMVar_ID_106311 Human_SNP_ID_308717349 m1A Human chr7 + 6272552 6272552 6272552 CCCGCAGCCGGCGAGCCGGGGGCCGGCAGCAGAGGGGCCGCGGGCTGGGGACGCCGCCGGAGGGA CCCGCAGCCGGCGAGCCGGGGGCCGGCAGCAGGGGGGCCGCGGGCTGGGGACGCCGCCGGAGGGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:6272476..6272650 26863410 MeRIP-seq:(Medium) rs1178088452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106312 RMVar_ID_106312 Human_SNP_ID_308743121 m1A Human chr7 + 6348686 6348686 6348686 GAAGATGAGCAGCGTGCGAGTCAGCCCCTTGCAGAAGACCCCATAGGAGCGGGCGGCGGCCGAGC GAAGATGAGCAGCGTGCGAGTCAGCCCCTTGCGGAAGACCCCATAGGAGCGGGCGGCGGCCGAGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6348650..6348734 26863196 MeRIP-seq:(Medium) rs1207396868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106313 RMVar_ID_106313 Human_SNP_ID_308743257 m1A Human chr7 - 6348891 6348891 6348891 CTTCTCCGAGCGTGACGTGCGGACTCCGCTCCACTGCGGCCCGCCCGCCCGCCGGTCTAGCCGCC CTTCTCCGAGCGTGACGTGCGGACTCCGCTCCGCTGCGGCCCGCCCGCCCGCCGGTCTAGCCGCC T C FAM220A,AC009412.1 Ensembl:ENSG00000178397,Ensembl:ENSG00000286075 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6348841..6348933 26863196 MeRIP-seq:(Medium) rs1282037930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4964422,Human_RBP_ID_5269762,Human_RBP_ID_5513553 Human_Splice_Rec_841977 106314 RMVar_ID_106314 Human_SNP_ID_308743258 m1A Human chr7 - 6348891 6348891 6348891 CTTCTCCGAGCGTGACGTGCGGACTCCGCTCCACTGCGGCCCGCCCGCCCGCCGGTCTAGCCGCC CTTCTCCGAGCGTGACGTGCGGACTCCGCTCCCCTGCGGCCCGCCCGCCCGCCGGTCTAGCCGCC T G FAM220A,AC009412.1 Ensembl:ENSG00000178397,Ensembl:ENSG00000286075 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6348841..6348933 26863196 MeRIP-seq:(Medium) rs1282037930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4964422,Human_RBP_ID_5269762,Human_RBP_ID_5513553 Human_Splice_Rec_841977 106315 RMVar_ID_106315 Human_SNP_ID_308751958 m1A Human chr7 - 6374661 6374661 6374661 AGATAGGAAGCGGCGGGCTCGGGGCGCGGCGGACGGGCGCGCGGCTTGCGGGCGGCGGGGCGCTG AGATAGGAAGCGGCGGGCTCGGGGCGCGGCGGCCGGGCGCGCGGCTTGCGGGCGGCGGGGCGCTG T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:6374565..6374721 26863410 MeRIP-seq:(Medium) rs1467220930 Functional Loss SNV dbSNP153 33..33 33 - - - 106316 RMVar_ID_106316 Human_SNP_ID_308752097 m1A Human chr7 - 6375006 6375006 6375006 AAAGCCGGAGGGTGGAGTTCACTTTTCCCTCTAGCCGGCGAGCGGCGAGGCCCTCCTCCATCGAG AAAGCCGGAGGGTGGAGTTCACTTTTCCCTCTGGCCGGCGAGCGGCGAGGCCCTCCTCCATCGAG T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:6375003..6375104 32194978 MeRIP-seq:(Medium) rs993331471 Functional Loss SNV dbSNP153 33..33 33 - - - 106317 RMVar_ID_106317 Human_SNP_ID_308756683 m1A Human chr7 - 6387203 6387203 6387203 AGTAGGCAAGTTTTACCTACAGCTCTAAAGAGAAAGAGAAAAAAGGTTGCTTAGTCAACATGAAT AGTAGGCAAGTTTTACCTACAGCTCTAAAGAGTAAGAGAAAAAAGGTTGCTTAGTCAACATGAAT T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:6387201..6387250 32194978 MeRIP-seq:(Medium) rs780736307 Functional Loss SNV dbSNP153 33..33 33 - - - 106318 RMVar_ID_106318 Human_SNP_ID_308779163 m1A Human chr7 + 6447905 6447905 6447905 AGACCCCGCGCGCCGTTCACCGAGAACAAACCAGCACCCTCCGGACGCCGCCACCAAATTATCGG AGACCCCGCGCGCCGTTCACCGAGAACAAACCGGCACCCTCCGGACGCCGCCACCAAATTATCGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:6447781..6447950 26863196 MeRIP-seq:(Medium) rs1156664892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106319 RMVar_ID_106319 Human_SNP_ID_308785706 m1A Human chr7 - 6466270 6466270 6466270 TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTATTTATGATCAGCAAGACTGGGGAGGCCGAGAC TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTTTTTATGATCAGCAAGACTGGGGAGGCCGAGAC T A KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2230263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253472,Human_RBP_ID_17314452,Human_RBP_ID_17426891,Human_RBP_ID_17543174,Human_RBP_ID_21517222,Human_RBP_ID_22774275,Human_RBP_ID_24438899,Human_RBP_ID_24517036,Human_RBP_ID_26830184,Human_RBP_ID_27115550 Human_Splice_Rec_842180,Human_Splice_Rec_842184 Human_miRNA_ID_2611028,Human_miRNA_ID_2611029 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_243666,RMVar_hsa_circ_115442,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_91216,RMVar_hsa_circ_243667,RMVar_hsa_circ_243670,RMVar_hsa_circ_316068,RMVar_hsa_circ_343940,RMVar_hsa_circ_272548,RMVar_hsa_circ_243669 106320 RMVar_ID_106320 Human_SNP_ID_308785707 m1A Human chr7 - 6466270 6466270 6466270 TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTATTTATGATCAGCAAGACTGGGGAGGCCGAGAC TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTGTTTATGATCAGCAAGACTGGGGAGGCCGAGAC T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2230263 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_253472,Human_RBP_ID_17314452,Human_RBP_ID_17426891,Human_RBP_ID_17543174,Human_RBP_ID_21517222,Human_RBP_ID_22774275,Human_RBP_ID_24438899,Human_RBP_ID_24517036,Human_RBP_ID_26830184,Human_RBP_ID_27115550 Human_Splice_Rec_842180,Human_Splice_Rec_842184 Human_miRNA_ID_2611028,Human_miRNA_ID_2611029 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_243666,RMVar_hsa_circ_115442,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_91216,RMVar_hsa_circ_243667,RMVar_hsa_circ_243670,RMVar_hsa_circ_316068,RMVar_hsa_circ_343940,RMVar_hsa_circ_272548,RMVar_hsa_circ_243669 106321 RMVar_ID_106321 Human_SNP_ID_308785708 m1A Human chr7 - 6466270 6466270 6466270 TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTATTTATGATCAGCAAGACTGGGGAGGCCGAGAC TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTCTTTATGATCAGCAAGACTGGGGAGGCCGAGAC T G KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2230263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253472,Human_RBP_ID_17314452,Human_RBP_ID_17426891,Human_RBP_ID_17543174,Human_RBP_ID_21517222,Human_RBP_ID_22774275,Human_RBP_ID_24438899,Human_RBP_ID_24517036,Human_RBP_ID_26830184,Human_RBP_ID_27115550 Human_Splice_Rec_842180,Human_Splice_Rec_842184 Human_miRNA_ID_2611028,Human_miRNA_ID_2611029 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_243666,RMVar_hsa_circ_115442,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_91216,RMVar_hsa_circ_243667,RMVar_hsa_circ_243670,RMVar_hsa_circ_316068,RMVar_hsa_circ_343940,RMVar_hsa_circ_272548,RMVar_hsa_circ_243669 106322 RMVar_ID_106322 Human_SNP_ID_308786856 m1A Human chr7 + 6469752 6469752 6469752 TACACTGTGGCATAGGAGCAGGCAAGGTAGATAACCTACAAATAAAAGAAAAAACACCAGGTGTC TACACTGTGGCATAGGAGCAGGCAAGGTAGATTACCTACAAATAAAAGAAAAAACACCAGGTGTC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr7:6466167..6469789;chr7:6469701..6469775 32194978 MeRIP-seq:(Medium) rs145710275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106323 RMVar_ID_106323 Human_SNP_ID_308788285 m1A Human chr7 + 6474277 6474277 6474277 AAGACCAGTGCAAACAGAAGCTGGCTTTTCCCAGAAATACCTAGAGAAACAGAAGGGAAGTATTA AAGACCAGTGCAAACAGAAGCTGGCTTTTCCCGGAAATACCTAGAGAAACAGAAGGGAAGTATTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6474226..6474300 26863196 MeRIP-seq:(Medium) rs747384596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106324 RMVar_ID_106324 Human_SNP_ID_308788288 m1A Human chr7 + 6474283 6474283 6474283 AGTGCAAACAGAAGCTGGCTTTTCCCAGAAATACCTAGAGAAACAGAAGGGAAGTATTAGAAGGG AGTGCAAACAGAAGCTGGCTTTTCCCAGAAATGCCTAGAGAAACAGAAGGGAAGTATTAGAAGGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr7:6474226..6474353;chr7:6474251..6474300 26863410,26863196 MeRIP-seq:(Medium) rs771198290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106325 RMVar_ID_106325 Human_SNP_ID_308791189 m1A Human chr7 - 6484051 6484051 6484051 CGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTGACTGGGGACCTGTCCCACCTG CGCCGACCGCCACCGCCGCCGCCGCCATGAACTTTTTCCGGCTGACTGGGGACCTGTCCCACCTG T A KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6484001..6484200 26863196 MeRIP-seq:(Medium) rs778358542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84865,Human_RBP_ID_687022,Human_RBP_ID_4956162,Human_RBP_ID_7750487,Human_RBP_ID_9337039,Human_RBP_ID_9404263,Human_RBP_ID_16192614,Human_RBP_ID_17313492,Human_RBP_ID_18195933,Human_RBP_ID_18884564,Human_RBP_ID_22110646,Human_RBP_ID_22534306,Human_RBP_ID_24221444,Human_RBP_ID_26830192,Human_RBP_ID_27533075 Human_Splice_Rec_842109,Human_Splice_Rec_842173,Human_Splice_Rec_842175,Human_Splice_Rec_842187,Human_Splice_Rec_842193,Human_Splice_Rec_842199 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106326 RMVar_ID_106326 Human_SNP_ID_308791190 m1A Human chr7 - 6484051 6484051 6484051 CGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTGACTGGGGACCTGTCCCACCTG CGCCGACCGCCACCGCCGCCGCCGCCATGAACGTTTTCCGGCTGACTGGGGACCTGTCCCACCTG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6484001..6484200 26863196 MeRIP-seq:(Medium) rs778358542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84865,Human_RBP_ID_687022,Human_RBP_ID_4956162,Human_RBP_ID_7750487,Human_RBP_ID_9337039,Human_RBP_ID_9404263,Human_RBP_ID_16192614,Human_RBP_ID_17313492,Human_RBP_ID_18195933,Human_RBP_ID_18884564,Human_RBP_ID_22110646,Human_RBP_ID_22534306,Human_RBP_ID_24221444,Human_RBP_ID_26830192,Human_RBP_ID_27533075 Human_Splice_Rec_842109,Human_Splice_Rec_842173,Human_Splice_Rec_842175,Human_Splice_Rec_842187,Human_Splice_Rec_842193,Human_Splice_Rec_842199 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106327 RMVar_ID_106327 Human_SNP_ID_308791198 m1A Human chr7 - 6484072 6484063 6484072 AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTG AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCC_________GCCGCCATGAACATTTTCCGGCTG CGGCGGCGGT C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:6483951..6484175 26863410 MeRIP-seq:(Medium) rs1348960933 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_253475,Human_RBP_ID_4955650,Human_RBP_ID_9212215,Human_RBP_ID_17426900,Human_RBP_ID_22534306,Human_RBP_ID_26830193 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106328 RMVar_ID_106328 Human_SNP_ID_308791201 m1A Human chr7 - 6484072 6484066 6484072 AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTG AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCC______GCCGCCGCCATGAACATTTTCCGGCTG CGGCGGT C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:6483951..6484175 26863410 MeRIP-seq:(Medium) rs768533386 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_253475,Human_RBP_ID_4955650,Human_RBP_ID_9212215,Human_RBP_ID_17426900,Human_RBP_ID_22534306,Human_RBP_ID_26830193 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106329 RMVar_ID_106329 Human_SNP_ID_308791209 m1A Human chr7 - 6484072 6484072 6484072 AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTG AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCGCCGCCGCCGCCGCCATGAACATTTTCCGGCTG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:6483951..6484175 26863410 MeRIP-seq:(Medium) rs759519707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253475,Human_RBP_ID_4955650,Human_RBP_ID_9212215,Human_RBP_ID_17426900,Human_RBP_ID_22534306,Human_RBP_ID_26830193 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106330 RMVar_ID_106330 Human_SNP_ID_308791210 m1A Human chr7 - 6484072 6484072 6484072 AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCACCGCCGCCGCCGCCATGAACATTTTCCGGCTG AGCCCCGGGGCCGCCGCGCTGCGCCGACCGCCCCCGCCGCCGCCGCCATGAACATTTTCCGGCTG T G KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:6483951..6484175 26863410 MeRIP-seq:(Medium) rs759519707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253475,Human_RBP_ID_4955650,Human_RBP_ID_9212215,Human_RBP_ID_17426900,Human_RBP_ID_22534306,Human_RBP_ID_26830193 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106331 RMVar_ID_106331 Human_SNP_ID_308791245 m1A Human chr7 - 6484112 6484112 6484112 CGCCGCTTCCTCTCAGGGGCCGCCGCCTCCTGAGCCGCCCAGCCCCGGGGCCGCCGCGCTGCGCC CGCCGCTTCCTCTCAGGGGCCGCCGCCTCCTGCGCCGCCCAGCCCCGGGGCCGCCGCGCTGCGCC T G KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding exon,5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:6484025..6484162 26863410 MeRIP-seq:(Medium) rs1319474331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253475,Human_RBP_ID_793526,Human_RBP_ID_4946464,Human_RBP_ID_17426900,Human_RBP_ID_22534245,Human_RBP_ID_26830193 Human_miRNA_ID_2269007 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 106332 RMVar_ID_106332 Human_SNP_ID_308820595 m1A Human chr7 - 6577500 6577500 6577500 CAAGCTTCCCACAGCCCCGCGGAGGCGGCCTTACCGCCAGCCGCTGGGCTCCGGCGCCTCCCGGG CAAGCTTCCCACAGCCCCGCGGAGGCGGCCTTGCCGCCAGCCGCTGGGCTCCGGCGCCTCCCGGG T C RF00017-4508,RF00017-4520,RF00017-4490 RNACentral:URS000093D619,RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6577482..6577681 26863196 MeRIP-seq:(Medium) rs1360213579 Functional Loss SNV dbSNP153 33..33 33 - - - 106333 RMVar_ID_106333 Human_SNP_ID_308822433 m1A Human chr7 + 6583412 6583412 6583412 GTGAGGTGCTCTACTTGTGATTTAAGGAAACCAGCTCGATCCAAGCACTGCAGTGAGTGTGGCTC GTGAGGTGCTCTACTTGTGATTTAAGGAAACCTGCTCGATCCAAGCACTGCAGTGAGTGTGGCTC A T ZDHHC4 Ensembl:ENSG00000136247 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:6583361..6583460 32194978 MeRIP-seq:(Medium) rs138558386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2045536,Human_RBP_ID_18108776,Human_RBP_ID_19020587 Human_Splice_Rec_842327,Human_Splice_Rec_842341,Human_Splice_Rec_842357,Human_Splice_Rec_842371,Human_Splice_Rec_842407,Human_Splice_Rec_842439 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_97477,RMVar_hsa_circ_79051,RMVar_hsa_circ_96510,RMVar_hsa_circ_86701,RMVar_hsa_circ_243677,RMVar_hsa_circ_307301,RMVar_hsa_circ_243679,RMVar_hsa_circ_243680,RMVar_hsa_circ_333529,RMVar_hsa_circ_271401,RMVar_hsa_circ_243681,RMVar_hsa_circ_243682,RMVar_hsa_circ_275087,RMVar_hsa_circ_317715,RMVar_hsa_circ_91553,RMVar_hsa_circ_316937,RMVar_hsa_circ_243684,RMVar_hsa_circ_243685,RMVar_hsa_circ_335116,RMVar_hsa_circ_243687,RMVar_hsa_circ_59411,RMVar_hsa_circ_82074,RMVar_hsa_circ_243688,RMVar_hsa_circ_243689 106334 RMVar_ID_106334 Human_SNP_ID_308824526 m1A Human chr7 - 6590100 6590100 6590100 TGCTCAGGGGGCCATCGCTGCTGCCGCCGGCCAGCAGGCGCCCGAAGGTCCGACTGCGGCGCCGC TGCTCAGGGGGCCATCGCTGCTGCCGCCGGCCGGCAGGCGCCCGAAGGTCCGACTGCGGCGCCGC T C RF00017-4508,RF00017-4520,RF00017-4490 RNACentral:URS000093D619,RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6590051..6591683 26863196 MeRIP-seq:(Medium) rs1182437808 Functional Loss SNV dbSNP153 33..33 33 - - - 106335 RMVar_ID_106335 Human_SNP_ID_308824676 m1A Human chr7 + 6590363 6590363 6590363 CGCCAAGGAGGTGTTGTACCACCTGGACATCTACTTCAGCAGCCAGCTGCAGAGCGCGCCGCTGC CGCCAAGGAGGTGTTGTACCACCTGGACATCTGCTTCAGCAGCCAGCTGCAGAGCGCGCCGCTGC A G C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:6590313..6590463 32194978 MeRIP-seq:(Medium) rs1319052761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3850552,Human_RBP_ID_4946995 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_125979,RMVar_hsa_circ_243692 106336 RMVar_ID_106336 Human_SNP_ID_308824677 m1A Human chr7 + 6590363 6590363 6590363 CGCCAAGGAGGTGTTGTACCACCTGGACATCTACTTCAGCAGCCAGCTGCAGAGCGCGCCGCTGC CGCCAAGGAGGTGTTGTACCACCTGGACATCTTCTTCAGCAGCCAGCTGCAGAGCGCGCCGCTGC A T C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:6590313..6590463 32194978 MeRIP-seq:(Medium) rs1319052761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3850552,Human_RBP_ID_4946995 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_125979,RMVar_hsa_circ_243692 106337 RMVar_ID_106337 Human_SNP_ID_308828413 m1A Human chr7 + 6600146 6600146 6600146 AACTCCACCTCAGCGTCCTGCAAGTGCTCATGACGCTGCAGCTGCACCTGACCGAGAAGAATCTG AACTCCACCTCAGCGTCCTGCAAGTGCTCATGTCGCTGCAGCTGCACCTGACCGAGAAGAATCTG A T C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:6600098..6600248 32194978 MeRIP-seq:(Medium) rs773021506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_687386,Human_RBP_ID_2045569,Human_RBP_ID_16198843,Human_RBP_ID_24222349,Human_RBP_ID_27359316 Human_Splice_Rec_842464 Human_miRNA_ID_2012239,Human_miRNA_ID_2012240,Human_miRNA_ID_2758611,Human_miRNA_ID_2758612 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_62347,RMVar_hsa_circ_125979,RMVar_hsa_circ_243692,RMVar_hsa_circ_110083,RMVar_hsa_circ_243696,RMVar_hsa_circ_243694,RMVar_hsa_circ_317817,RMVar_hsa_circ_42189,RMVar_hsa_circ_243698,RMVar_hsa_circ_371527,RMVar_hsa_circ_312239,RMVar_hsa_circ_243697 106338 RMVar_ID_106338 Human_SNP_ID_308831111 m1A Human chr7 + 6608106 6608101 6608107 CCACCCCGCCGCCCACCCCGCCCTGCCCACGCATCCCGGCCACACCTTCATCTCCGGCGTGACCT CCACCCCGCCGCCCACCCCGCCCTGCCC______CCCGGCCACACCTTCATCTCCGGCGTGACCT CACGCAT C C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:6607987..6608131 26863196 MeRIP-seq:(Medium) rs866826741 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_27533205 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694,RMVar_hsa_circ_89127,RMVar_hsa_circ_243699 106339 RMVar_ID_106339 Human_SNP_ID_308831114 m1A Human chr7 + 6608106 6608103 6608107 CCACCCCGCCGCCCACCCCGCCCTGCCCACGCATCCCGGCCACACCTTCATCTCCGGCGTGACCT CCACCCCGCCGCCCACCCCGCCCTGCCCAC____CCCGGCCACACCTTCATCTCCGGCGTGACCT CGCAT C C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:6607987..6608131 26863196 MeRIP-seq:(Medium) rs1212933060 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_27533205 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694,RMVar_hsa_circ_89127,RMVar_hsa_circ_243699 106340 RMVar_ID_106340 Human_SNP_ID_308831118 m1A Human chr7 + 6608106 6608105 6608107 CCACCCCGCCGCCCACCCCGCCCTGCCCACGCATCCCGGCCACACCTTCATCTCCGGCGTGACCT CCACCCCGCCGCCCACCCCGCCCTGCCCACGC__CCCGGCCACACCTTCATCTCCGGCGTGACCT CAT C C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:6607987..6608131 26863196 MeRIP-seq:(Medium) rs1246538726 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_27533205 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694,RMVar_hsa_circ_89127,RMVar_hsa_circ_243699 106341 RMVar_ID_106341 Human_SNP_ID_308831119 m1A Human chr7 + 6608106 6608106 6608106 CCACCCCGCCGCCCACCCCGCCCTGCCCACGCATCCCGGCCACACCTTCATCTCCGGCGTGACCT CCACCCCGCCGCCCACCCCGCCCTGCCCACGCCTCCCGGCCACACCTTCATCTCCGGCGTGACCT A C C7orf26 Ensembl:ENSG00000146576 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:6607987..6608131 26863196 MeRIP-seq:(Medium) rs773101949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27533205 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694,RMVar_hsa_circ_89127,RMVar_hsa_circ_243699 106342 RMVar_ID_106342 Human_SNP_ID_308831135 m1A Human chr7 - 6608120 6608120 6608120 GGGCCTGAAGGGAAAGGTCACGCCGGAGATGAAGGTGTGGCCGGGATGCGTGGGCAGGGCGGGGT GGGCCTGAAGGGAAAGGTCACGCCGGAGATGACGGTGTGGCCGGGATGCGTGGGCAGGGCGGGGT T G RF00017-4508,RF00017-4520,RF00017-4490 RNACentral:URS000093D619,RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:6608118..6608307 26863196 MeRIP-seq:(Medium) rs1299997380 Functional Loss SNV dbSNP153 33..33 33 - - - 106343 RMVar_ID_106343 Human_SNP_ID_308840300 m1A Human chr7 - 6636654 6636654 6636654 GGCGACCCCAGGAACCCAGGGAGGGGTCGGTGAGCTCAGCGGCCACCCCCAGACCCCCACCCACA GGCGACCCCAGGAACCCAGGGAGGGGTCGGTGCGCTCAGCGGCCACCCCCAGACCCCCACCCACA T G RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6636645..6636840 26863196 MeRIP-seq:(Medium) rs60232048 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14555 106344 RMVar_ID_106344 Human_SNP_ID_308840339 m1A Human chr7 - 6636787 6636785 6636788 ATGGGTGGACTGTGGCGGTTGAGTGCAGGAGGAGACTGGGGTTGTGGAGCCCGCACTTGGAGGGA ATGGGTGGACTGTGGCGGTTGAGTGCAGGAG___ACTGGGGTTGTGGAGCCCGCACTTGGAGGGA TCTC T RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6636665..6636842 26863196 MeRIP-seq:(Medium) rs1470976957 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5479755 106345 RMVar_ID_106345 Human_SNP_ID_308840581 m1A Human chr7 - 6637381 6637381 6637381 CACCGGGGCCGGGGCCTGCGGGCCGGCGGCGGACCCCGCGCTACACAAAGTGACGGCCCGGGAGC CACCGGGGCCGGGGCCTGCGGGCCGGCGGCGGGCCCCGCGCTACACAAAGTGACGGCCCGGGAGC T C RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr7:6637351..6637623;chr7:6637345..6638031 26863196 MeRIP-seq:(Medium) rs1202045191 Functional Loss SNV dbSNP153 33..33 33 - - - 106346 RMVar_ID_106346 Human_SNP_ID_308840584 m1A Human chr7 - 6637414 6637387 6637414 GCGCGGGCCGGGCTGGCCGAGCCACGGGCCGGACACCGGGGCCGGGGCCTGCGGGCCGGCGGCGG GCGCGGGCCGGGCTGGCCGAGCCACGGGCCGG___________________________CGGCGG GCCGGCCCGCAGGCCCCGGCCCCGGTGT G RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:6637363..6637900;chr7:6637370..6641882 26863196 MeRIP-seq:(Medium) rs1470206419 Functional Loss DEL dbSNP153 33..59 33 - - - 106347 RMVar_ID_106347 Human_SNP_ID_308840590 m1A Human chr7 + 6637397 6637397 6637397 TTTGTGTAGCGCGGGGTCCGCCGCCGGCCCGCAGGCCCCGGCCCCGGTGTCCGGCCCGTGGCTCG TTTGTGTAGCGCGGGGTCCGCCGCCGGCCCGCGGGCCCCGGCCCCGGTGTCCGGCCCGTGGCTCG A G ZNF316 Ensembl:ENSG00000205903 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6637356..6637931 26863196 MeRIP-seq:(Medium) rs993224641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4955659,Human_RBP_ID_5242971,Human_RBP_ID_9337041,Human_RBP_ID_18426280,Human_RBP_ID_18503889 Human_Splice_Rec_842495,Human_Splice_Rec_842511 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106348 RMVar_ID_106348 Human_SNP_ID_308840627 m1A Human chr7 - 6637511 6637511 6637511 CCGGCCCCGCCGCCGCCGCCGCCCCCGAGCGCAAGCCCGGCCCGCCCGCACCTGCCGCCCGCGCC CCGGCCCCGCCGCCGCCGCCGCCCCCGAGCGCGAGCCCGGCCCGCCCGCACCTGCCGCCCGCGCC T C RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:6637412..6637615 26863196 MeRIP-seq:(Medium) rs1198273859 Functional Loss SNV dbSNP153 33..33 33 - - - 106349 RMVar_ID_106349 Human_SNP_ID_308841885 m1A Human chr7 + 6641888 6641888 6641888 CTGTCTCTCCTCCTAGCCCCGTTGTGCCTTGCAAGTGCCTGCATCCTGTCTGTGCTGAGACCTCT CTGTCTCTCCTCCTAGCCCCGTTGTGCCTTGCGAGTGCCTGCATCCTGTCTGTGCTGAGACCTCT A G ZNF316 Ensembl:ENSG00000205903 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6641806..6641980 26863196 MeRIP-seq:(Medium) rs757633532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4964677,Human_RBP_ID_19019450 Human_Splice_Rec_842500,Human_Splice_Rec_842501,Human_Splice_Rec_842516 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_26192,RMVar_hsa_circ_24079,RMVar_hsa_circ_19996 106350 RMVar_ID_106350 Human_SNP_ID_308845365 m1A Human chr7 + 6653227 6653227 6653227 GGACCCTGGGCCAGAGGGATCTGAAGTTGGCGAGGCGGACGGAGAGGCGGAGGCCGCGGCCGAGG GGACCCTGGGCCAGAGGGATCTGAAGTTGGCGTGGCGGACGGAGAGGCGGAGGCCGCGGCCGAGG A T ZNF316 Ensembl:ENSG00000205903 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6653059..6653387 26863196 MeRIP-seq:(Medium) rs1377421015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794085,Human_RBP_ID_8914313,Human_RBP_ID_27533236 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106351 RMVar_ID_106351 Human_SNP_ID_308846170 m1A Human chr7 - 6655351 6655348 6655351 TGACCTCGGTGCAAGTGTGGGTAGAGAAGAGGAGGCGGCTCGAGAATAAGGCTTCAAACTCCCTC TGACCTCGGTGCAAGTGTGGGTAGAGAAGAGG___CGGCTCGAGAATAAGGCTTCAAACTCCCTC GCCT G RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6655300..6655427 26863196 MeRIP-seq:(Medium) rs1013398868 Functional Loss DEL dbSNP153 33..35 33 - - - 106352 RMVar_ID_106352 Human_SNP_ID_308846172 m1A Human chr7 - 6655351 6655351 6655351 TGACCTCGGTGCAAGTGTGGGTAGAGAAGAGGAGGCGGCTCGAGAATAAGGCTTCAAACTCCCTC TGACCTCGGTGCAAGTGTGGGTAGAGAAGAGGCGGCGGCTCGAGAATAAGGCTTCAAACTCCCTC T G RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6655300..6655427 26863196 MeRIP-seq:(Medium) rs371418094 Functional Loss SNV dbSNP153 33..33 33 - - - 106353 RMVar_ID_106353 Human_SNP_ID_308861397 m1A Human chr7 + 6702377 6702377 6702377 ACACACACGCACACACACCAGATTCATCTCCCAAACTCCACACACACACACACAACCAGATTCGT ACACACACGCACACACACCAGATTCATCTCCCCAACTCCACACACACACACACAACCAGATTCGT A C AC073343.2 Ensembl:ENSG00000228010 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:6702210..6702533;chr7:6702212..6702544;chr7:6702218..6702543 26863196 MeRIP-seq:(Medium) rs1179263191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106354 RMVar_ID_106354 Human_SNP_ID_308861718 m1A Human chr7 + 6702961 6702961 6702961 CACACACACACACCAGATTCGTGTCCCAAAACACACACACACACACACACACCTGCCTTCTTGAT CACACACACACACCAGATTCGTGTCCCAAAACGCACACACACACACACACACCTGCCTTCTTGAT A G AC073343.2 Ensembl:ENSG00000228010 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6702911..6703139 26863196 MeRIP-seq:(Medium) rs1050217121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106355 RMVar_ID_106355 Human_SNP_ID_308861721 m1A Human chr7 + 6702971 6702971 6702971 CACCAGATTCGTGTCCCAAAACACACACACACACACACACACCTGCCTTCTTGATGCTGCCACTC CACCAGATTCGTGTCCCAAAACACACACACACCCACACACACCTGCCTTCTTGATGCTGCCACTC A C AC073343.2 Ensembl:ENSG00000228010 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:6702921..6703121 26863196 MeRIP-seq:(Medium) rs1458511156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106356 RMVar_ID_106356 Human_SNP_ID_308863030 m1A Human chr7 - 6706738 6706738 6706738 ACGACCCCCGGAGCCGACGGCGCTGGGGCCCAAGGGGCCGGCCGGGCGGTGACGACGGCGGAGGC ACGACCCCCGGAGCCGACGGCGCTGGGGCCCAGGGGGCCGGCCGGGCGGTGACGACGGCGGAGGC T C ZNF12 Ensembl:ENSG00000164631 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6705214..6706913 26863196 MeRIP-seq:(Medium) rs1277700420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794861,Human_RBP_ID_4955664,Human_RBP_ID_8914918 106357 RMVar_ID_106357 Human_SNP_ID_308863031 m1A Human chr7 - 6706739 6706739 6706739 CACGACCCCCGGAGCCGACGGCGCTGGGGCCCAAGGGGCCGGCCGGGCGGTGACGACGGCGGAGG CACGACCCCCGGAGCCGACGGCGCTGGGGCCCGAGGGGCCGGCCGGGCGGTGACGACGGCGGAGG T C ZNF12 Ensembl:ENSG00000164631 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:6705214..6706916 26863196 MeRIP-seq:(Medium) rs1562604305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794861,Human_RBP_ID_4955664,Human_RBP_ID_8914918 106358 RMVar_ID_106358 Human_SNP_ID_308869767 m1A Human chr7 + 6729950 6729950 6729950 TATGTGGGCCAGGGTTCGCACGGGCCGGGTGGAGGCTTGAGCGGGGACCCCCGAGCGTGAGCCCC TATGTGGGCCAGGGTTCGCACGGGCCGGGTGGGGGCTTGAGCGGGGACCCCCGAGCGTGAGCCCC A G PMS2CL Ensembl:ENSG00000187953 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6729821..6730280 26863196 MeRIP-seq:(Medium) rs1294648850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842816,Human_RBP_ID_953090,Human_RBP_ID_9312150,Human_RBP_ID_9337051,Human_RBP_ID_9438829,Human_RBP_ID_10370141,Human_RBP_ID_17200250,Human_RBP_ID_17543568,Human_RBP_ID_21992332 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106359 RMVar_ID_106359 Human_SNP_ID_308869771 m1A Human chr7 + 6729964 6729964 6729964 TTCGCACGGGCCGGGTGGAGGCTTGAGCGGGGACCCCCGAGCGTGAGCCCCTGAGCCGGCGGCCC TTCGCACGGGCCGGGTGGAGGCTTGAGCGGGGTCCCCCGAGCGTGAGCCCCTGAGCCGGCGGCCC A T PMS2CL Ensembl:ENSG00000187953 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:6729815..6730262 26863196 MeRIP-seq:(Medium) rs953446821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842816,Human_RBP_ID_953090,Human_RBP_ID_3867531,Human_RBP_ID_4958005,Human_RBP_ID_5222444,Human_RBP_ID_8915260,Human_RBP_ID_9312150,Human_RBP_ID_9337051,Human_RBP_ID_9438829,Human_RBP_ID_10370141,Human_RBP_ID_17200250,Human_RBP_ID_17316539,Human_RBP_ID_17543568,Human_RBP_ID_17672256,Human_RBP_ID_17674074,Human_RBP_ID_18960703,Human_RBP_ID_19139679,Human_RBP_ID_21992332,Human_RBP_ID_22529878,Human_RBP_ID_26794376 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 106360 RMVar_ID_106360 Human_SNP_ID_308875285 m1A Human chr7 - 6749542 6749542 6749542 GCTCCATCCCACCCACTCCCCACGTGGCCCCCAGCTGCTGCTCTCCCCAGCGGCCGCAGCCACCG GCTCCATCCCACCCACTCCCCACGTGGCCCCCCGCTGCTGCTCTCCCCAGCGGCCGCAGCCACCG T G RF00017-4520,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS0000922AF7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:6749428..6749557 26863196 MeRIP-seq:(Medium) rs971024286 Functional Loss SNV dbSNP153 33..33 33 - - - 106361 RMVar_ID_106361 Human_SNP_ID_309012277 m1A Human chr7 + 7182692 7182692 7182692 TGCTGCCGCTGCCGGGGAATAATCTGGGCGGCAGCGGGCGGCCTCGGCTAGCGGCCACGAGCCAC TGCTGCCGCTGCCGGGGAATAATCTGGGCGGCGGCGGGCGGCCTCGGCTAGCGGCCACGAGCCAC A G C1GALT1 Ensembl:ENSG00000106392 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:7182648..7182738 26863196 MeRIP-seq:(Medium) rs1215100880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254187,Human_RBP_ID_4955667,Human_RBP_ID_8944150,Human_RBP_ID_9337711 106362 RMVar_ID_106362 Human_SNP_ID_309012278 m1A Human chr7 + 7182692 7182692 7182692 TGCTGCCGCTGCCGGGGAATAATCTGGGCGGCAGCGGGCGGCCTCGGCTAGCGGCCACGAGCCAC TGCTGCCGCTGCCGGGGAATAATCTGGGCGGCTGCGGGCGGCCTCGGCTAGCGGCCACGAGCCAC A T C1GALT1 Ensembl:ENSG00000106392 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:7182648..7182738 26863196 MeRIP-seq:(Medium) rs1215100880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254187,Human_RBP_ID_4955667,Human_RBP_ID_8944150,Human_RBP_ID_9337711 106363 RMVar_ID_106363 Human_SNP_ID_309120983 m1A Human chr7 + 7567130 7567130 7567130 TCTCGACTCTCGGGAGCGCCGCGGCCGCAGCGAGGGGCCGGAGATAGCCTAGTTGAAAGGCCCGG TCTCGACTCTCGGGAGCGCCGCGGCCGCAGCGTGGGGCCGGAGATAGCCTAGTTGAAAGGCCCGG A T MIOS Ensembl:ENSG00000164654 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:7566943..7567242;chr7:7567079..7567219;chr7:7567008..7567232 26863196 MeRIP-seq:(Medium) rs1052980455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956183,Human_RBP_ID_18425968 106364 RMVar_ID_106364 Human_SNP_ID_309123700 m1A Human chr7 + 7576547 7576547 7576547 GTGCAGTGGACCCAGAGGGTAGAGAGCATAGCACATTATTATGGCTGAAACAGAGCATGAGAGAG GTGCAGTGGACCCAGAGGGTAGAGAGCATAGCCCATTATTATGGCTGAAACAGAGCATGAGAGAG A C MIOS Ensembl:ENSG00000164654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:7576497..7576700 26863196 MeRIP-seq:(Medium) rs1482390048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4940,RMVar_hsa_circ_38028,RMVar_hsa_circ_243738 106365 RMVar_ID_106365 Human_SNP_ID_309208536 m1A Human chr7 + 7883015 7883011 7883015 GAGGAAGAAGAAGAAGGAGGAGGAGAAGGAGGAAGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GAGGAAGAAGAAGAAGGAGGAGGAGAAGG____AGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GAGGA G AC007161.3,UMAD1 Ensembl:ENSG00000283549,Ensembl:ENSG00000219545 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:7882965..7883110 26863196 MeRIP-seq:(Medium) rs768344868 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5105317 RMVar_hsa_circ_243749,RMVar_hsa_circ_243748,RMVar_hsa_circ_243750 106366 RMVar_ID_106366 Human_SNP_ID_309208542 m1A Human chr7 + 7883015 7883014 7883015 GAGGAAGAAGAAGAAGGAGGAGGAGAAGGAGGAAGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GAGGAAGAAGAAGAAGGAGGAGGAGAAGGAGG_AGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GA G AC007161.3,UMAD1 Ensembl:ENSG00000283549,Ensembl:ENSG00000219545 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:7882965..7883110 26863196 MeRIP-seq:(Medium) rs372062472 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5105317 GWAS_ID_14556,GWAS_ID_14557,GWAS_ID_14558,GWAS_ID_14559,GWAS_ID_14560,GWAS_ID_14561 RMVar_hsa_circ_243749,RMVar_hsa_circ_243748,RMVar_hsa_circ_243750 106367 RMVar_ID_106367 Human_SNP_ID_309230585 m1A Human chr7 - 7968865 7968865 7968865 AGAAAGGGCCTCGAGGTGCTGGCGCTCCTCGGAGTCCGCGCCACCGCAAACGCCGCCGCCGCCGC AGAAAGGGCCTCGAGGTGCTGGCGCTCCTCGGTGTCCGCGCCACCGCAAACGCCGCCGCCGCCGC T A GLCCI1-DT Ensembl:ENSG00000233108 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:7968820..7969063 26863196 MeRIP-seq:(Medium) rs149254242 Functional Loss SNV dbSNP153 33..33 33 - - - 106368 RMVar_ID_106368 Human_SNP_ID_309230786 m1A Human chr7 - 7969315 7969315 7969315 GGCTCTGCGGGCCCTGGACGCCGCCGGCCGACACGGAGGCGCGGGGCGGGAGGCGCGCGAGCGTG GGCTCTGCGGGCCCTGGACGCCGCCGGCCGACGCGGAGGCGCGGGGCGGGAGGCGCGCGAGCGTG T C GLCCI1-DT Ensembl:ENSG00000233108 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:7969266..7969379 26863196 MeRIP-seq:(Medium) rs774852995 Functional Loss SNV dbSNP153 33..33 33 - - - 106369 RMVar_ID_106369 Human_SNP_ID_309230820 m1A Human chr7 - 7969359 7969359 7969359 TGAGAGGAACTGGAGGAGGAGGAGGAGGAGGCAGTGGACATGGTGGCTCTGCGGGCCCTGGACGC TGAGAGGAACTGGAGGAGGAGGAGGAGGAGGCGGTGGACATGGTGGCTCTGCGGGCCCTGGACGC T C GLCCI1-DT Ensembl:ENSG00000233108 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:7969092..7969742;chr7:7969274..7969383 26863196 MeRIP-seq:(Medium) rs1185383715 Functional Loss SNV dbSNP153 33..33 33 - - - 106370 RMVar_ID_106370 Human_SNP_ID_309230853 m1A Human chr7 - 7969401 7969401 7969401 GCGGCGCTGCGCCTCATCCTCTGCGACGGGGGATGAGGGGTCTGAGAGGAACTGGAGGAGGAGGA GCGGCGCTGCGCCTCATCCTCTGCGACGGGGGGTGAGGGGTCTGAGAGGAACTGGAGGAGGAGGA T C GLCCI1-DT Ensembl:ENSG00000233108 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:7969351..7969546 26863196 MeRIP-seq:(Medium) rs767630070 Functional Loss SNV dbSNP153 33..33 33 - - - 106371 RMVar_ID_106371 Human_SNP_ID_309261087 m1A Human chr7 + 8078707 8078704 8078707 CAAGGTCAGAGGAACTGGAGGAAAGGGGCTGAAGAAGAGTCAACAGCATTTGGTGGCCAATTAGA CAAGGTCAGAGGAACTGGAGGAAAGGGGCT___GAAGAGTCAACAGCATTTGGTGGCCAATTAGA TGAA T GLCCI1 Ensembl:ENSG00000106415 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:8078697..8078788 26863196 MeRIP-seq:(Medium) rs1413574043 Functional Loss DEL dbSNP153 31..33 33 - - - Human_Splice_Rec_843444 RMVar_hsa_circ_316816,RMVar_hsa_circ_243752 106372 RMVar_ID_106372 Human_SNP_ID_309282840 m1A Human chr7 - 8152690 8152690 8152690 GTGGAGGAGGTGATGGTGGTAGTGGTGGGGGTAGTGGTGATGAAGGAGATAATGGTGGTGGTGGT GTGGAGGAGGTGATGGTGGTAGTGGTGGGGGTGGTGGTGATGAAGGAGATAATGGTGGTGGTGGT T C ICA1 Ensembl:ENSG00000003147 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:8152593..8152706 26863196 MeRIP-seq:(Medium) rs1317130679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310664,RMVar_hsa_circ_339961,RMVar_hsa_circ_334242,RMVar_hsa_circ_41393 106373 RMVar_ID_106373 Human_SNP_ID_310088815 m1A Human chr7 + 10938896 10938896 10938896 TCCAGTTCCAATAAATACAAAGAGGGGGATCAACTAAACCAAACACAAAATAGAATAACCATCTT TCCAGTTCCAATAAATACAAAGAGGGGGATCAGCTAAACCAAACACAAAATAGAATAACCATCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:10938793..10938955 26863196 MeRIP-seq:(Medium) rs1562544679 Functional Loss SNV dbSNP153 33..33 33 - - - 106374 RMVar_ID_106374 Human_SNP_ID_310089239 m1A Human chr7 + 10940090 10940090 10940090 GTTTGCGGCAGAGGTCTCCGACTGGAAAGGAGAGAACCGACCTAGCCACCAGGCCCTAAGCTAAA GTTTGCGGCAGAGGTCTCCGACTGGAAAGGAGTGAACCGACCTAGCCACCAGGCCCTAAGCTAAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:10939971..10940175 26863196 MeRIP-seq:(Medium) rs1437328682 Functional Loss SNV dbSNP153 33..33 33 - - - 106375 RMVar_ID_106375 Human_SNP_ID_310089272 m1A Human chr7 - 10940114 10940114 10940114 CGTAGTGTCTCATTGCAGATAATTTTTAGCTTAGGGCCTGGTGGCTAGGTCGGTTCTCTCCTTTC CGTAGTGTCTCATTGCAGATAATTTTTAGCTTCGGGCCTGGTGGCTAGGTCGGTTCTCTCCTTTC T G NDUFA4 Ensembl:ENSG00000189043 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:10939944..10940175 26863196 MeRIP-seq:(Medium) rs576206075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_86143,Human_RBP_ID_253811,Human_RBP_ID_673065,Human_RBP_ID_1680402,Human_RBP_ID_2033049,Human_RBP_ID_4921175,Human_RBP_ID_5327808,Human_RBP_ID_5480303,Human_RBP_ID_7676431,Human_RBP_ID_8654650,Human_RBP_ID_9337060,Human_RBP_ID_15975069,Human_RBP_ID_17426914,Human_RBP_ID_17543178,Human_RBP_ID_22463446,Human_RBP_ID_24184050,Human_RBP_ID_26830221 Human_Splice_Rec_843863,Human_Splice_Rec_843877 RMVar_hsa_circ_112993,RMVar_hsa_circ_243776 106376 RMVar_ID_106376 Human_SNP_ID_310100829 m1A Human chr7 + 10982585 10982585 10982585 AATGGAAAAGAAGGAAGAAGAAGAAAATGGAGAAAGACCTAGAAAGAAAAAGGAGAAAGAGAAGG AATGGAAAAGAAGGAAGAAGAAGAAAATGGAGGAAGACCTAGAAAGAAAAAGGAGAAAGAGAAGG A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:10982447..10982748 26863196 MeRIP-seq:(Medium) rs1297105025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_216380,Human_RBP_ID_3039503,Human_RBP_ID_22366546,Human_RBP_ID_23070872,Human_RBP_ID_24548876,Human_RBP_ID_26133419 RMVar_hsa_circ_77825,RMVar_hsa_circ_96750,RMVar_hsa_circ_374190,RMVar_hsa_circ_243777,RMVar_hsa_circ_120333,RMVar_hsa_circ_15921,RMVar_hsa_circ_320849,RMVar_hsa_circ_243778,RMVar_hsa_circ_243779,RMVar_hsa_circ_243780,RMVar_hsa_circ_367967,RMVar_hsa_circ_368099,RMVar_hsa_circ_327679,RMVar_hsa_circ_283811,RMVar_hsa_circ_288313,RMVar_hsa_circ_37242,RMVar_hsa_circ_243781,RMVar_hsa_circ_243782 106377 RMVar_ID_106377 Human_SNP_ID_310100847 m1A Human chr7 + 10982624 10982613 10982625 TAGAAAGAAAAAGGAGAAAGAGAAGGAAAAAGAAAAGGAAAAGGAGAAAGAGAAGGAAAGAGAGA TAGAAAGAAAAAGGAGAAAGAG____________AAGGAAAAGGAGAAAGAGAAGGAAAGAGAGA GAAGGAAAAAGAA G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:10982456..10982756 26863196 MeRIP-seq:(Medium) rs765487069 Functional Loss DEL dbSNP153 23..34 33 - - - Human_RBP_ID_217349,Human_RBP_ID_954228,Human_RBP_ID_1690908,Human_RBP_ID_3039505,Human_RBP_ID_22366546,Human_RBP_ID_23070874,Human_RBP_ID_24548876,Human_RBP_ID_24554936,Human_RBP_ID_26133421,Human_RBP_ID_26357594 RMVar_hsa_circ_77825,RMVar_hsa_circ_96750,RMVar_hsa_circ_374190,RMVar_hsa_circ_243777,RMVar_hsa_circ_120333,RMVar_hsa_circ_15921,RMVar_hsa_circ_320849,RMVar_hsa_circ_243778,RMVar_hsa_circ_243779,RMVar_hsa_circ_243780,RMVar_hsa_circ_367967,RMVar_hsa_circ_368099,RMVar_hsa_circ_327679,RMVar_hsa_circ_283811,RMVar_hsa_circ_288313,RMVar_hsa_circ_37242,RMVar_hsa_circ_243781,RMVar_hsa_circ_243782 106378 RMVar_ID_106378 Human_SNP_ID_310100985 m1A Human chr7 - 10982976 10982976 10982976 TCGTCTTCATCACTCCCGCTTCCCTCATCTTCATCATCCTCATTGTCTCCATCACTTCCCTCTTT TCGTCTTCATCACTCCCGCTTCCCTCATCTTCGTCATCCTCATTGTCTCCATCACTTCCCTCTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:10982876..10983086 26863196 MeRIP-seq:(Medium) rs776715855 Functional Loss SNV dbSNP153 33..33 33 - - - 106379 RMVar_ID_106379 Human_SNP_ID_310100986 m1A Human chr7 - 10982976 10982976 10982976 TCGTCTTCATCACTCCCGCTTCCCTCATCTTCATCATCCTCATTGTCTCCATCACTTCCCTCTTT TCGTCTTCATCACTCCCGCTTCCCTCATCTTCCTCATCCTCATTGTCTCCATCACTTCCCTCTTT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:10982876..10983086 26863196 MeRIP-seq:(Medium) rs776715855 Functional Loss SNV dbSNP153 33..33 33 - - - 106380 RMVar_ID_106380 Human_SNP_ID_310448958 m1A Human chr7 - 12211380 12211380 12211380 GCTGCGCAGTCCCGGGCTGCTTCGGCGCGGACAGGGCCGAGGACAGGGTCGTGGAGTCCACAGTC GCTGCGCAGTCCCGGGCTGCTTCGGCGCGGACTGGGCCGAGGACAGGGTCGTGGAGTCCACAGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:12211335..12211491 26863196 MeRIP-seq:(Medium) rs1037090088 Functional Loss SNV dbSNP153 33..33 33 - - - 106381 RMVar_ID_106381 Human_SNP_ID_426822074 m1A Human chr10 - 30047614 30047614 30047614 ATCGTAAGACGTCCGCGGGGAAAGGACATGTGAGTGACTCCGAAAGCCGCCGCAGCACACCGAGA ATCGTAAGACGTCCGCGGGGAAAGGACATGTGGGTGACTCCGAAAGCCGCCGCAGCACACCGAGA T C JCAD Ensembl:ENSG00000165757 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:30047612..30047697 26863410 MeRIP-seq:(Medium) rs374307085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376564 Human_Splice_Rec_1122577 RMVar_hsa_circ_360844 106382 RMVar_ID_106382 Human_SNP_ID_426822197 m1A Human chr10 - 30047873 30047873 30047873 CTAGTCACAAATAGAGCTCTCTGTTGTCCTGCAGTGCTGGGTCCTGCCACCACCATGGTTCCAGT CTAGTCACAAATAGAGCTCTCTGTTGTCCTGCTGTGCTGGGTCCTGCCACCACCATGGTTCCAGT T A JCAD Ensembl:ENSG00000165757 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:30047817..30047902 26863410 MeRIP-seq:(Medium) rs1175120306 Functional Loss SNV dbSNP153 33..33 33 - - - 106383 RMVar_ID_106383 Human_SNP_ID_426825006 m1A Human chr10 + 30059549 30059549 30059549 GCCGCCGCTCCGGCCGGCCGGGGACCAGCGCGACCCGCCCCGCCTGCAGCCGCCGAGGCCGAGCA GCCGCCGCTCCGGCCGGCCGGGGACCAGCGCGCCCCGCCCCGCCTGCAGCCGCCGAGGCCGAGCA A C lnc-MAP3K8-24,lnc-MAP3K8-24:2,RF00017-3663 RNACentral:URS0000D5C722,RNACentral:URS0000D59C31,RNACentral:URS0000926E08 lincRNA,lincRNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:30059480..30059557 26863196 MeRIP-seq:(Medium) rs1160184845 Functional Loss SNV dbSNP153 33..33 33 - - - 106384 RMVar_ID_106384 Human_SNP_ID_426894875 m1A Human chr10 - 30341614 30341614 30341614 TCATAGGCTTTGAAGACAAGATTCCCAAAAGGAGATTCTCTGAGATGCAAAATGAAAGACGAGAA TCATAGGCTTTGAAGACAAGATTCCCAAAAGGGGATTCTCTGAGATGCAAAATGAAAGACGAGAA T C MTPAP Ensembl:ENSG00000107951 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:30341563..30341683 26863196 MeRIP-seq:(Medium) rs1388314829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26808,Human_RBP_ID_862242,Human_RBP_ID_1765444,Human_RBP_ID_8333014,Human_RBP_ID_9343372,Human_RBP_ID_11347353 Human_Splice_Rec_1122586,Human_Splice_Rec_1122618,Human_Splice_Rec_1122634,Human_Splice_Rec_1122642 Human_miRNA_ID_1782714 RMVar_hsa_circ_46623,RMVar_hsa_circ_142896,RMVar_hsa_circ_64876,RMVar_hsa_circ_95683,RMVar_hsa_circ_127299,RMVar_hsa_circ_302109,RMVar_hsa_circ_142905,RMVar_hsa_circ_142907,RMVar_hsa_circ_347665,RMVar_hsa_circ_327092,RMVar_hsa_circ_142909,RMVar_hsa_circ_77555,RMVar_hsa_circ_142910,RMVar_hsa_circ_142908,RMVar_hsa_circ_303020,RMVar_hsa_circ_142911,RMVar_hsa_circ_142912 106385 RMVar_ID_106385 Human_SNP_ID_426896747 m1A Human chr10 - 30349224 30349224 30349224 GGCTCTTGACCCGTTTGAACCTGTGTGCCCGGAGAAGAACTCGAGTCCAGCGGCCTATCGTCAGG GGCTCTTGACCCGTTTGAACCTGTGTGCCCGGGGAAGAACTCGAGTCCAGCGGCCTATCGTCAGG T C MTPAP Ensembl:ENSG00000107951 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:30349151..30349275 26863196 MeRIP-seq:(Medium) rs1314754712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747260,Human_RBP_ID_1445977,Human_RBP_ID_1765448,Human_RBP_ID_4136211,Human_RBP_ID_5138085,Human_RBP_ID_5963068,Human_RBP_ID_11347504,Human_RBP_ID_18416098,Human_RBP_ID_22030220,Human_RBP_ID_23452816,Human_RBP_ID_24852667 Human_miRNA_ID_2541857,Human_miRNA_ID_2543732,Human_miRNA_ID_2545581,Human_miRNA_ID_2547437,Human_miRNA_ID_2551170,Human_miRNA_ID_2556576,Human_miRNA_ID_2558458,Human_miRNA_ID_2588877 RMVar_hsa_circ_95683,RMVar_hsa_circ_127299,RMVar_hsa_circ_142909,RMVar_hsa_circ_77555,RMVar_hsa_circ_142908,RMVar_hsa_circ_142912 106386 RMVar_ID_106386 Human_SNP_ID_426919300 m1A Human chr10 - 30434919 30434919 30434919 GACCTCTTTAGTCATGGGATAGAGTCCGGGTTACAAACTTGAATTTAGTTCCAGCCATTCACAAG GACCTCTTTAGTCATGGGATAGAGTCCGGGTTGCAAACTTGAATTTAGTTCCAGCCATTCACAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:30434918..30435039 26863196 MeRIP-seq:(Medium) rs903997811 Functional Loss SNV dbSNP153 33..33 33 - - - 106387 RMVar_ID_106387 Human_SNP_ID_427141949 m1A Human chr10 - 31318418 31318417 31318418 CCGCTTGCCAGCAGCCTCCTTAGTAGAGCGGAATGAGTAATACCCACACGGTGCTTGTCTCACTT CCGCTTGCCAGCAGCCTCCTTAGTAGAGCGGA_TGAGTAATACCCACACGGTGCTTGTCTCACTT AT A ZEB1-AS1 Ensembl:ENSG00000237036 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31318370..31318456 26863196 MeRIP-seq:(Medium) rs1415693912 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23452979 106388 RMVar_ID_106388 Human_SNP_ID_427142126 m1A Human chr10 - 31318945 31318945 31318945 GGTGTGGTGGGGAGAGGGAGGCGGATGCCGGGAAACCGTAGGGACGCGGTCAGAAAGGCGACGGG GGTGTGGTGGGGAGAGGGAGGCGGATGCCGGGCAACCGTAGGGACGCGGTCAGAAAGGCGACGGG T G ZEB1-AS1 Ensembl:ENSG00000237036 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:31318847..31319549;chr10:31318830..31319030 26863196 MeRIP-seq:(Medium) rs1283516579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863129,Human_RBP_ID_3366083,Human_RBP_ID_22030041 Human_Splice_Rec_1122945,Human_Splice_Rec_1122947,Human_Splice_Rec_1122951,Human_Splice_Rec_1122953,Human_Splice_Rec_1122955,Human_Splice_Rec_1122960 106389 RMVar_ID_106389 Human_SNP_ID_427142133 m1A Human chr10 - 31318989 31318958 31318990 CACTGCTGAATTTGAATTGAGGGGCGAGGGAAAAGTTTTCCTCAGGTGTGGTGGGGAGAGGGAGG CACTGCTGAATTTGAATTGAGGGGCGAGGGA________________________________GG CTCCCTCTCCCCACCACACCTGAGGAAAACTTT C ZEB1-AS1 Ensembl:ENSG00000237036 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:31318859..31319032 26863196 MeRIP-seq:(Medium) rs1554797271 Functional Loss DEL dbSNP153 32..63 33 - - - Human_RBP_ID_22030041 Human_Splice_Rec_1122945,Human_Splice_Rec_1122947,Human_Splice_Rec_1122951,Human_Splice_Rec_1122953,Human_Splice_Rec_1122955 106390 RMVar_ID_106390 Human_SNP_ID_427142141 m1A Human chr10 - 31318991 31318991 31318991 GGCACTGCTGAATTTGAATTGAGGGGCGAGGGAAAAGTTTTCCTCAGGTGTGGTGGGGAGAGGGA GGCACTGCTGAATTTGAATTGAGGGGCGAGGGTAAAGTTTTCCTCAGGTGTGGTGGGGAGAGGGA T A ZEB1-AS1 Ensembl:ENSG00000237036 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31318829..31319034 26863196 MeRIP-seq:(Medium) rs567832307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22030041 Human_Splice_Rec_1122945,Human_Splice_Rec_1122947,Human_Splice_Rec_1122951,Human_Splice_Rec_1122953,Human_Splice_Rec_1122955 106391 RMVar_ID_106391 Human_SNP_ID_427142487 m1A Human chr10 - 31319664 31319664 31319664 CGAAGGGCACAAGAGTGGGGAAAAGTGCGGAAAGAAGCAACAGCCGCTCCACCCGGGACCAGAAA CGAAGGGCACAAGAGTGGGGAAAAGTGCGGAAGGAAGCAACAGCCGCTCCACCCGGGACCAGAAA T C ZEB1-AS1 Ensembl:ENSG00000237036 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31319647..31319847 26863196 MeRIP-seq:(Medium) rs1052683153 Functional Loss SNV dbSNP153 33..33 33 - - - 106392 RMVar_ID_106392 Human_SNP_ID_427148341 m1A Human chr10 + 31342333 31342333 31342333 GAGCCAGTAGGAAAGGAATTGAGCCCAGGATTAGGGAGCTGATGGAAAATAGAGAAATTTTAGGT GAGCCAGTAGGAAAGGAATTGAGCCCAGGATTTGGGAGCTGATGGAAAATAGAGAAATTTTAGGT A T ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:31342331..31342510 26863196 MeRIP-seq:(Medium) rs991827363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5963393 RMVar_hsa_circ_86288,RMVar_hsa_circ_101171,RMVar_hsa_circ_142926,RMVar_hsa_circ_96757,RMVar_hsa_circ_142927,RMVar_hsa_circ_142928 106393 RMVar_ID_106393 Human_SNP_ID_427152737 m1A Human chr10 + 31361807 31361807 31361807 GGCACTCCTCACTTCACAGACAGGACGGCAGCAGGGCAGAGGCGCTCCTCATTTCCCAGACGGTG GGCACTCCTCACTTCACAGACAGGACGGCAGCGGGGCAGAGGCGCTCCTCATTTCCCAGACGGTG A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:31361805..31362133;chr10:31361795..31362161 26863196 MeRIP-seq:(Medium) rs1429690785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5907,RMVar_hsa_circ_86288,RMVar_hsa_circ_101171,RMVar_hsa_circ_142926,RMVar_hsa_circ_87610,RMVar_hsa_circ_96757,RMVar_hsa_circ_142927,RMVar_hsa_circ_142928,RMVar_hsa_circ_278749,RMVar_hsa_circ_336620,RMVar_hsa_circ_360534,RMVar_hsa_circ_282639,RMVar_hsa_circ_107723,RMVar_hsa_circ_142930,RMVar_hsa_circ_142932,RMVar_hsa_circ_142931,RMVar_hsa_circ_279038,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_142935,RMVar_hsa_circ_142936 106394 RMVar_ID_106394 Human_SNP_ID_427172388 m1A Human chr10 + 31439824 31439822 31439824 GAATGCAGTGAGCCGGGGTAAAGTAGAAGACAAAGTCTGAGAGAGACAGGTGAGGAGAGTCAGCC GAATGCAGTGAGCCGGGGTAAAGTAGAAGAC__AGTCTGAGAGAGACAGGTGAGGAGAGTCAGCC CAA C ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31439821..31439969 26863196 MeRIP-seq:(Medium) rs1309397812 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_87610,RMVar_hsa_circ_360534,RMVar_hsa_circ_142930,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_142942,RMVar_hsa_circ_298968,RMVar_hsa_circ_142946,RMVar_hsa_circ_292700,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941 106395 RMVar_ID_106395 Human_SNP_ID_427172390 m1A Human chr10 + 31439824 31439824 31439824 GAATGCAGTGAGCCGGGGTAAAGTAGAAGACAAAGTCTGAGAGAGACAGGTGAGGAGAGTCAGCC GAATGCAGTGAGCCGGGGTAAAGTAGAAGACAGAGTCTGAGAGAGACAGGTGAGGAGAGTCAGCC A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31439821..31439969 26863196 MeRIP-seq:(Medium) rs1395017962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87610,RMVar_hsa_circ_360534,RMVar_hsa_circ_142930,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_142942,RMVar_hsa_circ_298968,RMVar_hsa_circ_142946,RMVar_hsa_circ_292700,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941 106396 RMVar_ID_106396 Human_SNP_ID_427179610 m1A Human chr10 + 31461219 31461219 31461219 GGAGGAGCAGTGAAAGAGAAGGGAATGCTAAGAACTGCTGGGAGGATGACAGTAAGTCTGATTTT GGAGGAGCAGTGAAAGAGAAGGGAATGCTAAGTACTGCTGGGAGGATGACAGTAAGTCTGATTTT A T ZEB1 Ensembl:ENSG00000148516 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:31461022..31502382 26863196 MeRIP-seq:(Medium) rs1301814565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9361166,Human_RBP_ID_19046326 Human_Splice_Rec_1122973,Human_Splice_Rec_1122993,Human_Splice_Rec_1122999,Human_Splice_Rec_1123021,Human_Splice_Rec_1123031,Human_Splice_Rec_1123047,Human_Splice_Rec_1123065,Human_Splice_Rec_1123079,Human_Splice_Rec_1123093,Human_Splice_Rec_1123101,Human_Splice_Rec_1123117,Human_Splice_Rec_1123159,Human_Splice_Rec_1123171,Human_Splice_Rec_1123187,Human_Splice_Rec_1123201,Human_Splice_Rec_1123211,Human_Splice_Rec_1123227,Human_Splice_Rec_1123241,Human_Splice_Rec_1123251,Human_Splice_Rec_1123257 RMVar_hsa_circ_87610,RMVar_hsa_circ_360534,RMVar_hsa_circ_142930,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_142942,RMVar_hsa_circ_298968,RMVar_hsa_circ_142946,RMVar_hsa_circ_292700,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941,RMVar_hsa_circ_41010,RMVar_hsa_circ_277204,RMVar_hsa_circ_352540,RMVar_hsa_circ_362863,RMVar_hsa_circ_293595,RMVar_hsa_circ_274481,RMVar_hsa_circ_142947 106397 RMVar_ID_106397 Human_SNP_ID_427179612 m1A Human chr10 - 31461222 31461221 31461222 AAAAAAATCAGACTTACTGTCATCCTCCCAGCAGTTCTTAGCATTCCCTTCTCTTTCACTGCTCC AAAAAAATCAGACTTACTGTCATCCTCCCAGCCCTTCTTAGCATTCCCTTCTCTTTCACTGCTCC CT GG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:31461027..31461293 26863196 MeRIP-seq:(Medium) rs386742671 Functional Loss MNV dbSNP153 33..34 33 - - - 106398 RMVar_ID_106398 Human_SNP_ID_427188925 m1A Human chr10 + 31495702 31495702 31495702 GTAATGATCAGATCAGAGTAATTGGGATATCCAAAACTTTAAACATTTGTCTTTCGTTTGTATTA GTAATGATCAGATCAGAGTAATTGGGATATCCGAAACTTTAAACATTTGTCTTTCGTTTGTATTA A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:31495700..31495829 26863196 MeRIP-seq:(Medium) rs1371116767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360534,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941,RMVar_hsa_circ_41010,RMVar_hsa_circ_277204,RMVar_hsa_circ_352540,RMVar_hsa_circ_362863,RMVar_hsa_circ_293595 106399 RMVar_ID_106399 Human_SNP_ID_427190510 m1A Human chr10 - 31502284 31502284 31502284 TCTCACCACTAAGTTATTACAAAGGTTTTCTAAATAAGAAATTATTTATCTTGAGAGAACATATG TCTCACCACTAAGTTATTACAAAGGTTTTCTAGATAAGAAATTATTTATCTTGAGAGAACATATG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:31502283..31502376 26863196 MeRIP-seq:(Medium) rs899915970 Functional Loss SNV dbSNP153 33..33 33 - - - 106400 RMVar_ID_106400 Human_SNP_ID_427196318 m1A Human chr10 + 31527036 31527036 31527036 GAGGAAGAGGAGGAGGATAAAGAGATGGAAGAATTGCAGGAAGAAAAAGAATGTGAAAAACCACA GAGGAAGAGGAGGAGGATAAAGAGATGGAAGACTTGCAGGAAGAAAAAGAATGTGAAAAACCACA A C ZEB1 Ensembl:ENSG00000148516 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:31526918..31527213 26863196 MeRIP-seq:(Medium) rs1437137642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24550724 106401 RMVar_ID_106401 Human_SNP_ID_427196373 m1A Human chr10 + 31527134 31527134 31527134 AGTGGAAGAAGAAGAGGTAGAAGAGGCAGAGAATGAGGGAGAAGAAGCAAAAACTGAAGGTCTGA AGTGGAAGAAGAAGAGGTAGAAGAGGCAGAGAGTGAGGGAGAAGAAGCAAAAACTGAAGGTCTGA A G ZEB1 Ensembl:ENSG00000148516 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:31526902..31527250 26863196 MeRIP-seq:(Medium) rs1158050644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2214279,Human_RBP_ID_23453246,Human_RBP_ID_24542089,Human_RBP_ID_24550724,Human_RBP_ID_26317054 106402 RMVar_ID_106402 Human_SNP_ID_427296529 m1A Human chr10 - 31928720 31928720 31928720 GCGTCGTCGACCCGCAGCCGCGGGGCGGACTAAGAAGGGAGCCGCCTGCTGCGAGGCCGCCGGGC GCGTCGTCGACCCGCAGCCGCGGGGCGGACTAGGAAGGGAGCCGCCTGCTGCGAGGCCGCCGGGC T C ARHGAP12 Ensembl:ENSG00000165322 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:31928672..31928801 26863196 MeRIP-seq:(Medium) rs1467329861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135801,Human_RBP_ID_18416100,Human_RBP_ID_27802605 Human_Splice_Rec_1123305,Human_Splice_Rec_1123343,Human_Splice_Rec_1123379,Human_Splice_Rec_1123445 RMVar_hsa_circ_122044,RMVar_hsa_circ_142962 106403 RMVar_ID_106403 Human_SNP_ID_427296559 m1A Human chr10 - 31928767 31928767 31928767 GGGACGGGCCGGCCGCGGCCGTAGCCGTGTGAACGCTCTTCGGGCTCGCGTCGTCGACCCGCAGC GGGACGGGCCGGCCGCGGCCGTAGCCGTGTGAGCGCTCTTCGGGCTCGCGTCGTCGACCCGCAGC T C ARHGAP12 Ensembl:ENSG00000165322 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31928458..31928790 26863196 MeRIP-seq:(Medium) rs184905360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135801,Human_RBP_ID_18416101 Human_Splice_Rec_1123305,Human_Splice_Rec_1123343,Human_Splice_Rec_1123379,Human_Splice_Rec_1123445 RMVar_hsa_circ_122044,RMVar_hsa_circ_142962 106404 RMVar_ID_106404 Human_SNP_ID_427296671 m1A Human chr10 - 31928947 31928947 31928947 CCGCCGGGCGCCGCACCCCCTAGCCACCCCAGACCGTCCCGGAGACCCGCGCCCGCCCAGCTCGC CCGCCGGGCGCCGCACCCCCTAGCCACCCCAGTCCGTCCCGGAGACCCGCGCCCGCCCAGCTCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:31928937..31929120 26863196 MeRIP-seq:(Medium) rs1251947943 Functional Loss SNV dbSNP153 33..33 33 - - - 106405 RMVar_ID_106405 Human_SNP_ID_427306380 m1A Human chr10 - 31970082 31970082 31970082 GCCCCTCACCTCCCGGCCGGGGCGGCTGGCCGACCCCCCCCCCCCCCCCCCCCCCCCCCCCCCGG GCCCCTCACCTCCCGGCCGGGGCGGCTGGCCGCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:31969955..31970173 26863196 MeRIP-seq:(Medium) rs144082292 Functional Loss SNV dbSNP153 33..33 33 - - - 106406 RMVar_ID_106406 Human_SNP_ID_427321324 m1A Human chr10 - 32031267 32031267 32031267 AATTATTTTCTGTCCTATAGCTTTTGGCATCTACCAGAAGGGATCAAGACAATATGCAAGCTGAG AATTATTTTCTGTCCTATAGCTTTTGGCATCTGCCAGAAGGGATCAAGACAATATGCAAGCTGAG T C KIF5B Ensembl:ENSG00000170759 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:32031218..32033864 32194978 MeRIP-seq:(Medium) rs560751572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28064,Human_RBP_ID_864149,Human_RBP_ID_2214524,Human_RBP_ID_9360262,Human_RBP_ID_18593069,Human_RBP_ID_19510244,Human_RBP_ID_24541955,Human_RBP_ID_26317069,Human_RBP_ID_27802625 Human_Splice_Rec_1123554 Human_miRNA_ID_1264171,Human_miRNA_ID_2142221,Human_miRNA_ID_3046029 RMVar_hsa_circ_142975,RMVar_hsa_circ_107016,RMVar_hsa_circ_110863,RMVar_hsa_circ_106204,RMVar_hsa_circ_142977,RMVar_hsa_circ_142976,RMVar_hsa_circ_91128,RMVar_hsa_circ_342000,RMVar_hsa_circ_332969,RMVar_hsa_circ_124160,RMVar_hsa_circ_122734,RMVar_hsa_circ_88440,RMVar_hsa_circ_89032,RMVar_hsa_circ_64869,RMVar_hsa_circ_2144,RMVar_hsa_circ_14635,RMVar_hsa_circ_86990,RMVar_hsa_circ_142984,RMVar_hsa_circ_142986,RMVar_hsa_circ_142987,RMVar_hsa_circ_142985,RMVar_hsa_circ_142982,RMVar_hsa_circ_142983,RMVar_hsa_circ_372209,RMVar_hsa_circ_142981,RMVar_hsa_circ_344079,RMVar_hsa_circ_353119,RMVar_hsa_circ_23116,RMVar_hsa_circ_142993,RMVar_hsa_circ_142995,RMVar_hsa_circ_142994,RMVar_hsa_circ_49750,RMVar_hsa_circ_75725,RMVar_hsa_circ_282488,RMVar_hsa_circ_142997,RMVar_hsa_circ_298743,RMVar_hsa_circ_313002,RMVar_hsa_circ_340416,RMVar_hsa_circ_366815,RMVar_hsa_circ_59868,RMVar_hsa_circ_66839,RMVar_hsa_circ_68982,RMVar_hsa_circ_70449,RMVar_hsa_circ_143001,RMVar_hsa_circ_294101,RMVar_hsa_circ_348984,RMVar_hsa_circ_20932,RMVar_hsa_circ_367030,RMVar_hsa_circ_319851,RMVar_hsa_circ_55891,RMVar_hsa_circ_70093,RMVar_hsa_circ_59237,RMVar_hsa_circ_143003,RMVar_hsa_circ_143004,RMVar_hsa_circ_143005,RMVar_hsa_circ_366732,RMVar_hsa_circ_143002,RMVar_hsa_circ_368357,RMVar_hsa_circ_324285,RMVar_hsa_circ_143006 106407 RMVar_ID_106407 Human_SNP_ID_427324501 m1A Human chr10 - 32044009 32044009 32044009 GGGTACCTAGGGAGGTGTGAGGACAGGAAAGCAATTAAATACATGGTAGGTTGTACTTGGGACAA GGGTACCTAGGGAGGTGTGAGGACAGGAAAGCGATTAAATACATGGTAGGTTGTACTTGGGACAA T C KIF5B Ensembl:ENSG00000170759 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:32044007..32044089 26863196 MeRIP-seq:(Medium) rs756783965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805787,Human_RBP_ID_9589985 RMVar_hsa_circ_142975,RMVar_hsa_circ_110863,RMVar_hsa_circ_342000,RMVar_hsa_circ_142981,RMVar_hsa_circ_344079,RMVar_hsa_circ_142995,RMVar_hsa_circ_340416,RMVar_hsa_circ_59868,RMVar_hsa_circ_319851,RMVar_hsa_circ_143005,RMVar_hsa_circ_368357,RMVar_hsa_circ_74965,RMVar_hsa_circ_5081,RMVar_hsa_circ_319227,RMVar_hsa_circ_346107 106408 RMVar_ID_106408 Human_SNP_ID_427327437 m1A Human chr10 - 32056026 32056026 32056026 CCACAAGCCCTCAGGTCCGGCGCGTTCCCTGCAAGACTGAGCGGCGGGGAGTGGCTCCCGGCCGC CCACAAGCCCTCAGGTCCGGCGCGTTCCCTGCGAGACTGAGCGGCGGGGAGTGGCTCCCGGCCGC T C KIF5B Ensembl:ENSG00000170759 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:32055976..32056150 32194978 MeRIP-seq:(Medium) rs1333146361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136693,Human_RBP_ID_8765279,Human_RBP_ID_9254042,Human_RBP_ID_9273784,Human_RBP_ID_17776270,Human_RBP_ID_22881016 Human_miRNA_ID_2611245 RMVar_hsa_circ_142975,RMVar_hsa_circ_110863 106409 RMVar_ID_106409 Human_SNP_ID_427327545 m1A Human chr10 + 32056290 32056290 32056290 TTTACGGTCTGGGCGGACTGCGGGGGCTGGGGAGGTTCTGGGGACCGGGAGAGTGGCCACCTTCT TTTACGGTCTGGGCGGACTGCGGGGGCTGGGGCGGTTCTGGGGACCGGGAGAGTGGCCACCTTCT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:32056050..32056425 26863196 MeRIP-seq:(Medium) rs934311119 Functional Loss SNV dbSNP153 33..33 33 - - - 106410 RMVar_ID_106410 Human_SNP_ID_427327583 m1A Human chr10 - 32056372 32056372 32056372 GAGTGATCGGGCAGCAGTCGGCCGGCCAGCGGACGGCAGAGCGGGCGGACGGGTAGGCCCGGCCT GAGTGATCGGGCAGCAGTCGGCCGGCCAGCGGGCGGCAGAGCGGGCGGACGGGTAGGCCCGGCCT T C KIF5B Ensembl:ENSG00000170759 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:32055976..32056425;chr10:32056001..32056425 26863196 MeRIP-seq:(Medium) rs979068913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225459,Human_RBP_ID_747779,Human_RBP_ID_805326,Human_RBP_ID_4136217,Human_RBP_ID_8765283,Human_RBP_ID_9273788,Human_RBP_ID_22431987 Human_miRNA_ID_1967227,Human_miRNA_ID_2395303 RMVar_hsa_circ_142975,RMVar_hsa_circ_110863 106411 RMVar_ID_106411 Human_SNP_ID_427400622 m1A Human chr10 - 32338245 32338244 32338246 GGTGGATTTGAATGTACTAGATGGAGAGAGAGAATCCGAGGATGAACCTCCAAGTTGAGCAGCTG GGTGGATTTGAATGTACTAGATGGAGAGAGA__ATCCGAGGATGAACCTCCAAGTTGAGCAGCTG TTC T EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:32338194..32338331 26863196 MeRIP-seq:(Medium) rs1180271271 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11350895,Human_RBP_ID_27607046 106412 RMVar_ID_106412 Human_SNP_ID_427403241 m1A Human chr10 - 32347021 32347021 32347021 GCCCGGACGGCGGGCTCTGCGCTCCGCCCCTCAAGTCCCCGGCAGCGGTTGGCGAGTGGGGACCG GCCCGGACGGCGGGCTCTGCGCTCCGCCCCTCGAGTCCCCGGCAGCGGTTGGCGAGTGGGGACCG T C EPC1 Ensembl:ENSG00000120616 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:32346977..32347137 26863196 MeRIP-seq:(Medium) rs144258182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225794,Human_RBP_ID_4118193,Human_RBP_ID_5435395,Human_RBP_ID_9320528 106413 RMVar_ID_106413 Human_SNP_ID_427452025 m1A Human chr10 - 32548366 32548366 32548366 GATCACCTGCTCCGTCCTGAGTCACCCTGGTCACCTGCTCTGACCTGAATTATCTGTTCTGTAGC GATCACCTGCTCCGTCCTGAGTCACCCTGGTCTCCTGCTCTGACCTGAATTATCTGTTCTGTAGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:32548318..32548497 26863196 MeRIP-seq:(Medium) rs1488151094 Functional Loss SNV dbSNP153 33..33 33 - - - 106414 RMVar_ID_106414 Human_SNP_ID_427545654 m1A Human chr10 + 32912109 32912109 32912109 TCATCTGTGCTGCATTCACAATGTCTACCAACACGCCCTTCATTGCACCTGAAGAAACATGCCAA TCATCTGTGCTGCATTCACAATGTCTACCAACGCGCCCTTCATTGCACCTGAAGAAACATGCCAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:32911947..32912160 26863196 MeRIP-seq:(Medium) rs1175862320 Functional Loss SNV dbSNP153 33..33 33 - - - 106415 RMVar_ID_106415 Human_SNP_ID_427551751 m1A Human chr10 - 32935554 32935554 32935554 CTAATATAAGGCACATTTTACATTTCAGATGAATTTACAACCAATTTTCTGGATTGGACTGATCA CTAATATAAGGCACATTTTACATTTCAGATGAGTTTACAACCAATTTTCTGGATTGGACTGATCA T C ITGB1 Ensembl:ENSG00000150093 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:32935493..32935930 32194978 MeRIP-seq:(Medium) rs916061555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376985,Human_RBP_ID_982966,Human_RBP_ID_1260681,Human_RBP_ID_1765914,Human_RBP_ID_2215143,Human_RBP_ID_4136219,Human_RBP_ID_5459234,Human_RBP_ID_5965731,Human_RBP_ID_8760745,Human_RBP_ID_8997134,Human_RBP_ID_9360272,Human_RBP_ID_17459539,Human_RBP_ID_22639284,Human_RBP_ID_22735712,Human_RBP_ID_24808013 Human_Splice_Rec_1124182,Human_Splice_Rec_1124183,Human_Splice_Rec_1124211,Human_Splice_Rec_1124242,Human_Splice_Rec_1124243,Human_Splice_Rec_1124282,Human_Splice_Rec_1124283,Human_Splice_Rec_1124290,Human_Splice_Rec_1124291,Human_Splice_Rec_1124298,Human_Splice_Rec_1124299,Human_Splice_Rec_1124308,Human_Splice_Rec_1124309,Human_Splice_Rec_1124316,Human_Splice_Rec_1124317,Human_Splice_Rec_1124324,Human_Splice_Rec_1124325,Human_Splice_Rec_1124332,Human_Splice_Rec_1124333,Human_Splice_Rec_1124342,Human_Splice_Rec_1124343,Human_Splice_Rec_1124350,Human_Splice_Rec_1124351,Human_Splice_Rec_1124357,Human_Splice_Rec_1124366,Human_Splice_Rec_1124367,Human_Splice_Rec_1124378,Human_Splice_Rec_1124379 RMVar_hsa_circ_270269,RMVar_hsa_circ_51605,RMVar_hsa_circ_289320,RMVar_hsa_circ_335192,RMVar_hsa_circ_65919,RMVar_hsa_circ_35572,RMVar_hsa_circ_349797,RMVar_hsa_circ_16114 106416 RMVar_ID_106416 Human_SNP_ID_427882522 m1A Human chr10 + 34234424 34234424 34234424 CTCGGTAGGTTCATCTGCCACATACCTCTCTGATTTCTTCCCATACCACTCAACACACTGTAGCC CTCGGTAGGTTCATCTGCCACATACCTCTCTGGTTTCTTCCCATACCACTCAACACACTGTAGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:34234420..34234549 26863196 MeRIP-seq:(Medium) rs1201355787 Functional Loss SNV dbSNP153 33..33 33 - - - 106417 RMVar_ID_106417 Human_SNP_ID_427894408 m1A Human chr10 - 34284208 34284208 34284208 GCAAACATCGAAAAGATGACAAGATTGAGAAAACGGGTAAAATAAAAATACAGGAATCCTTTACA GCAAACATCGAAAAGATGACAAGATTGAGAAAGCGGGTAAAATAAAAATACAGGAATCCTTTACA T C PARD3 Ensembl:ENSG00000148498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:34284180..34284297 26863196 MeRIP-seq:(Medium) rs1173214595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1124730,Human_Splice_Rec_1124731,Human_Splice_Rec_1124776,Human_Splice_Rec_1124777,Human_Splice_Rec_1124824,Human_Splice_Rec_1124825,Human_Splice_Rec_1124872,Human_Splice_Rec_1124873,Human_Splice_Rec_1125004,Human_Splice_Rec_1125005,Human_Splice_Rec_1125048,Human_Splice_Rec_1125049,Human_Splice_Rec_1125062,Human_Splice_Rec_1125063 Human_miRNA_ID_2278096 RMVar_hsa_circ_143106,RMVar_hsa_circ_110908,RMVar_hsa_circ_118270,RMVar_hsa_circ_143102,RMVar_hsa_circ_101575,RMVar_hsa_circ_143103,RMVar_hsa_circ_360831,RMVar_hsa_circ_143101,RMVar_hsa_circ_290670,RMVar_hsa_circ_14051,RMVar_hsa_circ_54654,RMVar_hsa_circ_351924,RMVar_hsa_circ_366301,RMVar_hsa_circ_58624,RMVar_hsa_circ_37203,RMVar_hsa_circ_318543,RMVar_hsa_circ_334777,RMVar_hsa_circ_368810,RMVar_hsa_circ_358526,RMVar_hsa_circ_322657,RMVar_hsa_circ_69491,RMVar_hsa_circ_277852,RMVar_hsa_circ_280660,RMVar_hsa_circ_275695,RMVar_hsa_circ_143108,RMVar_hsa_circ_67463,RMVar_hsa_circ_143109,RMVar_hsa_circ_143107,RMVar_hsa_circ_29420,RMVar_hsa_circ_55561,RMVar_hsa_circ_320015,RMVar_hsa_circ_143105,RMVar_hsa_circ_299249,RMVar_hsa_circ_42446,RMVar_hsa_circ_143110,RMVar_hsa_circ_11124,RMVar_hsa_circ_143111 106418 RMVar_ID_106418 Human_SNP_ID_427901191 m1A Human chr10 + 34312371 34312371 34312371 ATCGCTTTGTTGTTCATCTCTTCTCGGGCTTCAGTTTGGCAAGGCTAAATGAGAGACACGGTACA ATCGCTTTGTTGTTCATCTCTTCTCGGGCTTCGGTTTGGCAAGGCTAAATGAGAGACACGGTACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:34312365..34312430 26863196 MeRIP-seq:(Medium) rs367916122 Functional Loss SNV dbSNP153 33..33 33 - - - 106419 RMVar_ID_106419 Human_SNP_ID_427902270 m1A Human chr10 - 34317207 34317207 34317207 ACCAAGAGAAAGGTGATAAGACTGATAGAAAAAAGGATAAAACTGGAAAAGAAAAGAAGAAAGAT ACCAAGAGAAAGGTGATAAGACTGATAGAAAAGAGGATAAAACTGGAAAAGAAAAGAAGAAAGAT T C PARD3 Ensembl:ENSG00000148498 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:34317101..34317307 26863196 MeRIP-seq:(Medium) rs766001258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27419,Human_RBP_ID_23454262 Human_miRNA_ID_2070430,Human_miRNA_ID_2070431,Human_miRNA_ID_2803346,Human_miRNA_ID_2803347 RMVar_hsa_circ_143106,RMVar_hsa_circ_110908,RMVar_hsa_circ_118270,RMVar_hsa_circ_143102,RMVar_hsa_circ_101575,RMVar_hsa_circ_143103,RMVar_hsa_circ_143101,RMVar_hsa_circ_290670,RMVar_hsa_circ_14051,RMVar_hsa_circ_54654,RMVar_hsa_circ_366301,RMVar_hsa_circ_58624,RMVar_hsa_circ_37203,RMVar_hsa_circ_318543,RMVar_hsa_circ_334777,RMVar_hsa_circ_368810,RMVar_hsa_circ_358526,RMVar_hsa_circ_322657,RMVar_hsa_circ_69491,RMVar_hsa_circ_277852,RMVar_hsa_circ_280660,RMVar_hsa_circ_143108,RMVar_hsa_circ_67463,RMVar_hsa_circ_143107,RMVar_hsa_circ_59130,RMVar_hsa_circ_29420,RMVar_hsa_circ_55561,RMVar_hsa_circ_320015,RMVar_hsa_circ_143105,RMVar_hsa_circ_299249,RMVar_hsa_circ_42446,RMVar_hsa_circ_143112,RMVar_hsa_circ_11124,RMVar_hsa_circ_143111,RMVar_hsa_circ_104631,RMVar_hsa_circ_303183,RMVar_hsa_circ_351361,RMVar_hsa_circ_353239,RMVar_hsa_circ_357519,RMVar_hsa_circ_351967,RMVar_hsa_circ_314510,RMVar_hsa_circ_276411,RMVar_hsa_circ_143113 106420 RMVar_ID_106420 Human_SNP_ID_428023476 m1A Human chr10 - 34791977 34791977 34791977 CTCAGGAGAGATTGGAGTGGAGTTGAAAAAGCAGGAAGCAGAGAGGGAAGTCCGTGTGTAACAAA CTCAGGAGAGATTGGAGTGGAGTTGAAAAAGCGGGAAGCAGAGAGGGAAGTCCGTGTGTAACAAA T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:34791962..34792054 26863196 MeRIP-seq:(Medium) rs1210589486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143135,RMVar_hsa_circ_126043 106421 RMVar_ID_106421 Human_SNP_ID_428029721 m1A Human chr10 - 34815207 34815186 34815207 GCTGCGGGCGCCGCGGCGGGGAGAGGCGAGGCAAGCCCCGGGCGAAGCGAGGCGAGGCGAGGGCG GCTGCGGGCGCCGCGGCGGGGAGAGGCGAGGC_____________________GAGGCGAGGGCG CGCCTCGCTTCGCCCGGGGCTT C PARD3 Ensembl:ENSG00000148498 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr10:34815107..34815290;chr10:34815159..34815315 26863410,26863196 MeRIP-seq:(Medium) rs1393436966 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_4135813,Human_RBP_ID_18416103 RMVar_hsa_circ_143135,RMVar_hsa_circ_126043 106422 RMVar_ID_106422 Human_SNP_ID_428029721 m1A Human chr10 - 34815206 34815186 34815207 CTGCGGGCGCCGCGGCGGGGAGAGGCGAGGCAAGCCCCGGGCGAAGCGAGGCGAGGCGAGGGCGG CTGCGGGCGCCGCGGCGGGGAGAGGCGAGGC_____________________GAGGCGAGGGCGG CGCCTCGCTTCGCCCGGGGCTT C PARD3 Ensembl:ENSG00000148498 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:34814946..34815310 26863196 MeRIP-seq:(Medium) rs1393436966 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_4135813,Human_RBP_ID_18416103 RMVar_hsa_circ_143135,RMVar_hsa_circ_126043 106423 RMVar_ID_106423 Human_SNP_ID_428031626 m1A Human chr10 + 34821843 34821840 34821844 AAGAAAGAAAAAGAGAAAGAAAGAAGAGATAAAGAGGAAGGAAGAAGGAGAGAGAAAAGGAAGGA AAGAAAGAAAAAGAGAAAGAAAGAAGAGAT____AGGAAGGAAGAAGGAGAGAGAAAAGGAAGGA TAAAG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:34821658..34822005 26863196 MeRIP-seq:(Medium) rs1291989090 Functional Loss DEL dbSNP153 31..34 33 - - - 106424 RMVar_ID_106424 Human_SNP_ID_428031629 m1A Human chr10 + 34821843 34821842 34821844 AAGAAAGAAAAAGAGAAAGAAAGAAGAGATAAAGAGGAAGGAAGAAGGAGAGAGAAAAGGAAGGA AAGAAAGAAAAAGAGAAAGAAAGAAGAGATAA__AGGAAGGAAGAAGGAGAGAGAAAAGGAAGGA AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:34821658..34822005 26863196 MeRIP-seq:(Medium) rs1414774938 Functional Loss DEL dbSNP153 33..34 33 - - - 106425 RMVar_ID_106425 Human_SNP_ID_428100042 m1A Human chr10 - 35090145 35090145 35090145 TAACCCCGCTGAGGGTCGGGGAGCCGGGCTGCAGGCGCCGGGAAACTTCCCTTCCCGGTTAATGG TAACCCCGCTGAGGGTCGGGGAGCCGGGCTGCGGGCGCCGGGAAACTTCCCTTCCCGGTTAATGG T C CUL2 Ensembl:ENSG00000108094 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:35090139..35090303 26863196 MeRIP-seq:(Medium) rs1191079714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4135814 RMVar_hsa_circ_267535 106426 RMVar_ID_106426 Human_SNP_ID_428100079 m1A Human chr10 + 35090263 35090263 35090263 CGAAGGAGTGAAAGACGAAGCCCCGGCGAGGAAGGTGGGCGGAGGCGGCGGCGGCGGCGGCTGTC CGAAGGAGTGAAAGACGAAGCCCCGGCGAGGAGGGTGGGCGGAGGCGGCGGCGGCGGCGGCTGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr10:35090218..35090318;chr10:35090207..35090320 26863196 MeRIP-seq:(Medium) rs1336060334 Functional Loss SNV dbSNP153 33..33 33 - - - 106427 RMVar_ID_106427 Human_SNP_ID_428100082 m1A Human chr10 - 35090266 35090266 35090266 GCTGACAGCCGCCGCCGCCGCCGCCTCCGCCCACCTTCCTCGCCGGGGCTTCGTCTTTCACTCCT GCTGACAGCCGCCGCCGCCGCCGCCTCCGCCCCCCTTCCTCGCCGGGGCTTCGTCTTTCACTCCT T G CUL2 Ensembl:ENSG00000108094 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35090220..35090321 26863196 MeRIP-seq:(Medium) rs1301317411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_377088,Human_RBP_ID_4118750,Human_RBP_ID_9320531 Human_Splice_Rec_1125275,Human_Splice_Rec_1125317,Human_Splice_Rec_1125397,Human_Splice_Rec_1125515 RMVar_hsa_circ_267535 106428 RMVar_ID_106428 Human_SNP_ID_428100086 m1A Human chr10 + 35090273 35090270 35090273 AAAGACGAAGCCCCGGCGAGGAAGGTGGGCGGAGGCGGCGGCGGCGGCGGCTGTCAGCTCGCGTT AAAGACGAAGCCCCGGCGAGGAAGGTGGGC___GGCGGCGGCGGCGGCGGCTGTCAGCTCGCGTT CGGA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:35090047..35090318 26863196 MeRIP-seq:(Medium) rs1471796103 Functional Loss DEL dbSNP153 31..33 33 - - - 106429 RMVar_ID_106429 Human_SNP_ID_428109216 m1A Human chr10 - 35127253 35127247 35127253 CCGGCTCCGCTCCGCCTCCTGCCTCCACCTCCACCTCCTGCGCCGCGTCGCCCGCTGCTGGGTCT CCGGCTCCGCTCCGCCTCCTGCCTCCACCTCC______TGCGCCGCGTCGCCCGCTGCTGGGTCT AGGAGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:35127202..35127523 26863196 MeRIP-seq:(Medium) rs551519932 Functional Loss DEL dbSNP153 33..38 33 - - - 106430 RMVar_ID_106430 Human_SNP_ID_428109224 m1A Human chr10 + 35127280 35127280 35127280 GGAGGTGGAGGTGGAGGCAGGAGGCGGAGCGGAGCCGGGTGCGGTGGAGCAGCAGAGGCCGAGCG GGAGGTGGAGGTGGAGGCAGGAGGCGGAGCGGCGCCGGGTGCGGTGGAGCAGCAGAGGCCGAGCG A C CREM Ensembl:ENSG00000095794 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35126872..35137852 26863196 MeRIP-seq:(Medium) rs1477367125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805638,Human_RBP_ID_863895 RMVar_hsa_circ_106095,RMVar_hsa_circ_143174 106431 RMVar_ID_106431 Human_SNP_ID_428113378 m1A Human chr10 + 35143296 35143296 35143296 GGGCTGGGAAACAGTAATTAAAATGAGAAGCCATGTTAGCTGAATAGGGTGGGAAGTGAAGAAAG GGGCTGGGAAACAGTAATTAAAATGAGAAGCCGTGTTAGCTGAATAGGGTGGGAAGTGAAGAAAG A G CREM Ensembl:ENSG00000095794 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:35143292..35143453 26863196 MeRIP-seq:(Medium) rs1288370237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106095,RMVar_hsa_circ_143175,RMVar_hsa_circ_55519,RMVar_hsa_circ_273448,RMVar_hsa_circ_355362,RMVar_hsa_circ_143174,RMVar_hsa_circ_353032,RMVar_hsa_circ_76865,RMVar_hsa_circ_50647 106432 RMVar_ID_106432 Human_SNP_ID_428161214 m1A Human chr10 - 35336599 35336599 35336599 GTTCAAGCCGGGGGCACGCGTGTCCGCGCCGGACGGCGGGACTAGCCGACGAGCGGGCGGGCAGC GTTCAAGCCGGGGGCACGCGTGTCCGCGCCGGCCGGCGGGACTAGCCGACGAGCGGGCGGGCAGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35336551..35336777 26863196 MeRIP-seq:(Medium) rs987224251 Functional Loss SNV dbSNP153 33..33 33 - - - 106433 RMVar_ID_106433 Human_SNP_ID_428161408 m1A Human chr10 + 35337016 35337016 35337016 CGTCCACCCGCGCCCCGCTCCCGGGGACTGGGAGAACAGGATAGCAGCAGGAGTCGGGGGGCCGC CGTCCACCCGCGCCCCGCTCCCGGGGACTGGGCGAACAGGATAGCAGCAGGAGTCGGGGGGCCGC A C CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:35336862..35337051 26863196 MeRIP-seq:(Medium) rs373946039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5313195 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 106434 RMVar_ID_106434 Human_SNP_ID_428161411 m1A Human chr10 + 35337024 35337024 35337024 CGCGCCCCGCTCCCGGGGACTGGGAGAACAGGATAGCAGCAGGAGTCGGGGGGCCGCCGAAGATG CGCGCCCCGCTCCCGGGGACTGGGAGAACAGGTTAGCAGCAGGAGTCGGGGGGCCGCCGAAGATG A T CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35336975..35337092 26863196 MeRIP-seq:(Medium) rs777053809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1446502,Human_RBP_ID_4118847,Human_RBP_ID_5313195,Human_RBP_ID_17345614 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 106435 RMVar_ID_106435 Human_SNP_ID_428161433 m1A Human chr10 - 35337084 35337084 35337084 GGAGTGGGCATTCCTCCGGAGCTTGGGACTGGACGACACGCAGCACGAGGTAGTGTTCCCCATCT GGAGTGGGCATTCCTCCGGAGCTTGGGACTGGTCGACACGCAGCACGAGGTAGTGTTCCCCATCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:35336923..35337093 26863196 MeRIP-seq:(Medium) rs1243700637 Functional Loss SNV dbSNP153 33..33 33 - - - 106436 RMVar_ID_106436 Human_SNP_ID_428174791 m1A Human chr10 - 35392547 35392547 35392547 CTGGCCATCTGTCAAAATCCTTACTCCCTTCAAGATCTGGTTCTAATTCCAATGCCTCTGAAGCT CTGGCCATCTGTCAAAATCCTTACTCCCTTCATGATCTGGTTCTAATTCCAATGCCTCTGAAGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35392544..35392754 26863196 MeRIP-seq:(Medium) rs1280229348 Functional Loss SNV dbSNP153 33..33 33 - - - 106437 RMVar_ID_106437 Human_SNP_ID_428177140 m1A Human chr10 + 35402584 35402584 35402584 GGTCTCCGTGATTTTGGAGGAAAGAGAAATGCAAAGCCAGCAATTGTTTGTTAAAGAAGGATTAG GGTCTCCGTGATTTTGGAGGAAAGAGAAATGCCAAGCCAGCAATTGTTTGTTAAAGAAGGATTAG A C CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:35402579..35402827 26863196 MeRIP-seq:(Medium) rs926399966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 106438 RMVar_ID_106438 Human_SNP_ID_428177840 m1A Human chr10 + 35405219 35405219 35405219 TTAAAAGGCCATGCTGTAACAGGCAAGTGACAACAGGTTTTAATCCTTTTAAAGCATGCTGTGGG TTAAAAGGCCATGCTGTAACAGGCAAGTGACAGCAGGTTTTAATCCTTTTAAAGCATGCTGTGGG A G CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35405216..35405522 26863196 MeRIP-seq:(Medium) rs1213599356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 106439 RMVar_ID_106439 Human_SNP_ID_428177849 m1A Human chr10 - 35405282 35405282 35405282 TGCACCCTTTACCATCCCATTAAAACCTAATCACCCTTATCCTGCTCAATGCCAATATCCCATCC TGCACCCTTTACCATCCCATTAAAACCTAATCCCCCTTATCCTGCTCAATGCCAATATCCCATCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35405279..35405404 26863196 MeRIP-seq:(Medium) rs1326936892 Functional Loss SNV dbSNP153 33..33 33 - - - 106440 RMVar_ID_106440 Human_SNP_ID_428179939 m1A Human chr10 + 35413084 35413081 35413085 TAGTCTTTTGGTATTGTGTTGGAGAGATAAGAAGGAAGGAACCAAAAAAGGAAGACACCAAGAGG TAGTCTTTTGGTATTGTGTTGGAGAGATAA____GAAGGAACCAAAAAAGGAAGACACCAAGAGG AGAAG A CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35413081..35413230 26863196 MeRIP-seq:(Medium) rs1230032011 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_22881437 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 106441 RMVar_ID_106441 Human_SNP_ID_428183661 m1A Human chr10 - 35428594 35428594 35428594 CATTCTCTCTCTCTCTCTCTGCCTTCACCCTTACCCCTTGCTTAAACCCCTTCAATGGCTTCTCA CATTCTCTCTCTCTCTCTCTGCCTTCACCCTTCCCCCTTGCTTAAACCCCTTCAATGGCTTCTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35428591..35428854 26863196 MeRIP-seq:(Medium) rs1161559568 Functional Loss SNV dbSNP153 33..33 33 - - - 106442 RMVar_ID_106442 Human_SNP_ID_428185480 m1A Human chr10 + 35435970 35435970 35435970 AGGAGGAAGTTAATTCTGGGTGGGAGGTGGTCAGCAGAAGTTCCAGAAAGGAAGGAAGTTCGGTT AGGAGGAAGTTAATTCTGGGTGGGAGGTGGTCTGCAGAAGTTCCAGAAAGGAAGGAAGTTCGGTT A T CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35435967..35436147 26863196 MeRIP-seq:(Medium) rs191379610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5969800 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349,RMVar_hsa_circ_351625,RMVar_hsa_circ_359488 106443 RMVar_ID_106443 Human_SNP_ID_428188568 m1A Human chr10 + 35449309 35449308 35449310 ATAGGGGCAGGGAGGGGGGTGAAGAGAGAGAGATGGTCCCGGCAGTCAGCGAGGGAGACATTTTG ATAGGGGCAGGGAGGGGGGTGAAGAGAGAGAG__GGTCCCGGCAGTCAGCGAGGGAGACATTTTG GAT G CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35449306..35449601 26863196 MeRIP-seq:(Medium) rs1471071133 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1815,Human_RBP_ID_23455553 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349,RMVar_hsa_circ_351625,RMVar_hsa_circ_359488 106444 RMVar_ID_106444 Human_SNP_ID_428188582 m1A Human chr10 + 35449349 35449349 35449349 GGCAGTCAGCGAGGGAGACATTTTGAGGAGAAAGTGGGCATCTCTAGTAAGATAAGGACTGAGAT GGCAGTCAGCGAGGGAGACATTTTGAGGAGAAGGTGGGCATCTCTAGTAAGATAAGGACTGAGAT A G CCNY Ensembl:ENSG00000108100 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:35449303..35449546 26863196 MeRIP-seq:(Medium) rs1408257499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1815 RMVar_hsa_circ_143181,RMVar_hsa_circ_80349,RMVar_hsa_circ_351625,RMVar_hsa_circ_359488 106445 RMVar_ID_106445 Human_SNP_ID_428188774 m1A Human chr10 - 35450017 35450017 35450017 TCTGCCCTCCAAAGCGCTTTCTGGCAAATCCCAGAGCTGATTAAATCTAACTCCCCATCTCCTCT TCTGCCCTCCAAAGCGCTTTCTGGCAAATCCCGGAGCTGATTAAATCTAACTCCCCATCTCCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:35450015..35450402 26863196 MeRIP-seq:(Medium) rs1004321498 Functional Loss SNV dbSNP153 33..33 33 - - - 106446 RMVar_ID_106446 Human_SNP_ID_428236406 m1A Human chr10 - 35638887 35638887 35638887 CCCTGGAGGAGGGGTGACCGCCACCTGATGGGATTGCACGGTTTGGGTATTCTTAATGACCAGGC CCCTGGAGGAGGGGTGACCGCCACCTGATGGGTTTGCACGGTTTGGGTATTCTTAATGACCAGGC T A FZD8 Ensembl:ENSG00000177283 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35638836..35638995 26863196 MeRIP-seq:(Medium) rs1292607497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5970124,Human_RBP_ID_8334256,Human_RBP_ID_8760827,Human_RBP_ID_18241248 106447 RMVar_ID_106447 Human_SNP_ID_428236407 m1A Human chr10 - 35638887 35638887 35638887 CCCTGGAGGAGGGGTGACCGCCACCTGATGGGATTGCACGGTTTGGGTATTCTTAATGACCAGGC CCCTGGAGGAGGGGTGACCGCCACCTGATGGGGTTGCACGGTTTGGGTATTCTTAATGACCAGGC T C FZD8 Ensembl:ENSG00000177283 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35638836..35638995 26863196 MeRIP-seq:(Medium) rs1292607497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5970124,Human_RBP_ID_8334256,Human_RBP_ID_8760827,Human_RBP_ID_18241248 106448 RMVar_ID_106448 Human_SNP_ID_428236733 m1A Human chr10 - 35639598 35639598 35639598 GGGCGTGTGGGTCTGGTCCGGCAAGACGCTGGAGTCCTGGCGCTCCCTGTGCACCCGCTGCTGCT GGGCGTGTGGGTCTGGTCCGGCAAGACGCTGGCGTCCTGGCGCTCCCTGTGCACCCGCTGCTGCT T G FZD8 Ensembl:ENSG00000177283 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:35639293..35639610 26863196 MeRIP-seq:(Medium) rs1457056344 Functional Loss SNV dbSNP153 33..33 33 - - - 106449 RMVar_ID_106449 Human_SNP_ID_428237067 m1A Human chr10 + 35640380 35640371 35640380 CCCGCGCCCGCCGCCGCGCCGCCCGCGCCCCCAGCGCCCCCCGCGCCCGGCGCGCCACCGCTGCA CCCGCGCCCGCCGCCGCGCCGCCC_________GCGCCCCCCGCGCCCGGCGCGCCACCGCTGCA CGCGCCCCCA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:35640287..35640398 26863196 MeRIP-seq:(Medium) rs1423225902 Functional Loss DEL dbSNP153 25..33 33 - - - 106450 RMVar_ID_106450 Human_SNP_ID_428237073 m1A Human chr10 + 35640380 35640380 35640380 CCCGCGCCCGCCGCCGCGCCGCCCGCGCCCCCAGCGCCCCCCGCGCCCGGCGCGCCACCGCTGCA CCCGCGCCCGCCGCCGCGCCGCCCGCGCCCCCCGCGCCCCCCGCGCCCGGCGCGCCACCGCTGCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:35640287..35640398 26863196 MeRIP-seq:(Medium) rs1470822394 Functional Loss SNV dbSNP153 33..33 33 - - - 106451 RMVar_ID_106451 Human_SNP_ID_428237178 m1A Human chr10 - 35640636 35640636 35640636 AGGCCAGATCGCTAACTGCGCGCTGCCCTGCCACAACCCCTTTTTCAGCCAGGACGAGCGCGCCT AGGCCAGATCGCTAACTGCGCGCTGCCCTGCCGCAACCCCTTTTTCAGCCAGGACGAGCGCGCCT T C FZD8 Ensembl:ENSG00000177283 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:35640535..35640723 26863196 MeRIP-seq:(Medium) rs1364896760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27405727 106452 RMVar_ID_106452 Human_SNP_ID_428237349 m1A Human chr10 + 35640998 35640998 35640998 TCGGTGCGGTTGTAGTCCATGCACAGCGTGTCAGGGTTGCCTTGCTCGGGCAGCCGGTCGCAGCG TCGGTGCGGTTGTAGTCCATGCACAGCGTGTCGGGGTTGCCTTGCTCGGGCAGCCGGTCGCAGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35640950..35641083 26863196 MeRIP-seq:(Medium) rs1212664200 Functional Loss SNV dbSNP153 33..33 33 - - - 106453 RMVar_ID_106453 Human_SNP_ID_428237504 m1A Human chr10 + 35641374 35641374 35641374 CCGAGGCGGCCGCAGCGCCGCTAGAGCGCTGCAGCAGCGCCAAGGCGGCCAGCAGCGAGGTCACT CCGAGGCGGCCGCAGCGCCGCTAGAGCGCTGCGGCAGCGCCAAGGCGGCCAGCAGCGAGGTCACT A G AL121749.2 Ensembl:ENSG00000287528 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:35641329..35641429 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1126149 106454 RMVar_ID_106454 Human_SNP_ID_428237733 m1A Human chr10 - 35641811 35641811 35641811 CGGCGGAGTCACCGCCGCCCGGCGCGGCGGGGAGAAGTGGTCGGGCGCGCGGAGAGGAGGCGAGC CGGCGGAGTCACCGCCGCCCGGCGCGGCGGGGCGAAGTGGTCGGGCGCGCGGAGAGGAGGCGAGC T G FZD8 Ensembl:ENSG00000177283 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:35641735..35641823 26863410 MeRIP-seq:(Medium) rs1431678529 Functional Loss SNV dbSNP153 33..33 33 - - - 106455 RMVar_ID_106455 Human_SNP_ID_428243946 m1A Human chr10 + 35667315 35667313 35667316 CCACCGCCACCACCATCATCACCACCACCACCATCATCACCACCATCACCACCACCACCACCATC CCACCGCCACCACCATCATCACCACCACCAC___CATCACCACCATCACCACCACCACCACCATC CCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35667214..35667354 26863196 MeRIP-seq:(Medium) rs1414454412 Functional Loss DEL dbSNP153 32..34 33 - - - 106456 RMVar_ID_106456 Human_SNP_ID_428243947 m1A Human chr10 + 35667315 35667315 35667315 CCACCGCCACCACCATCATCACCACCACCACCATCATCACCACCATCACCACCACCACCACCATC CCACCGCCACCACCATCATCACCACCACCACCGTCATCACCACCATCACCACCACCACCACCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35667214..35667354 26863196 MeRIP-seq:(Medium) rs111208326 Functional Loss SNV dbSNP153 33..33 33 - - - 106457 RMVar_ID_106457 Human_SNP_ID_428244094 m1A Human chr10 - 35667509 35667506 35667509 TGGTAGTGGTGATGGTGGTGATGATGGTGGTGATGGTGGTGATGGTGGTGGTGGTGATGATGGTG TGGTAGTGGTGATGGTGGTGATGATGGTGGTG___GTGGTGATGGTGGTGGTGGTGATGATGGTG CCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35667434..35667557 26863196 MeRIP-seq:(Medium) rs201085170 Functional Loss DEL dbSNP153 33..35 33 - - - 106458 RMVar_ID_106458 Human_SNP_ID_428244096 m1A Human chr10 - 35667509 35667509 35667509 TGGTAGTGGTGATGGTGGTGATGATGGTGGTGATGGTGGTGATGGTGGTGGTGGTGATGATGGTG TGGTAGTGGTGATGGTGGTGATGATGGTGGTGGTGGTGGTGATGGTGGTGGTGGTGATGATGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35667434..35667557 26863196 MeRIP-seq:(Medium) rs1180772488 Functional Loss SNV dbSNP153 33..33 33 - - - 106459 RMVar_ID_106459 Human_SNP_ID_428805929 m1A Human chr10 + 37857580 37857580 37857580 GTGGATAATTGTGTCTAATTCATTTGTCGCGGACCTGGCGCAGTCGCTCTCCCCCGCAGCCCCGC GTGGATAATTGTGTCTAATTCATTTGTCGCGGTCCTGGCGCAGTCGCTCTCCCCCGCAGCCCCGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:37857361..37857610 26863196 MeRIP-seq:(Medium) rs976653862 Functional Loss SNV dbSNP153 33..33 33 - - - 106460 RMVar_ID_106460 Human_SNP_ID_428805933 m1A Human chr10 + 37857589 37857589 37857589 TGTGTCTAATTCATTTGTCGCGGACCTGGCGCAGTCGCTCTCCCCCGCAGCCCCGCCTCCTCCCC TGTGTCTAATTCATTTGTCGCGGACCTGGCGCCGTCGCTCTCCCCCGCAGCCCCGCCTCCTCCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:37857471..37857673 26863196 MeRIP-seq:(Medium) rs929817143 Functional Loss SNV dbSNP153 33..33 33 - - - 106461 RMVar_ID_106461 Human_SNP_ID_428805934 m1A Human chr10 + 37857589 37857589 37857589 TGTGTCTAATTCATTTGTCGCGGACCTGGCGCAGTCGCTCTCCCCCGCAGCCCCGCCTCCTCCCC TGTGTCTAATTCATTTGTCGCGGACCTGGCGCTGTCGCTCTCCCCCGCAGCCCCGCCTCCTCCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:37857471..37857673 26863196 MeRIP-seq:(Medium) rs929817143 Functional Loss SNV dbSNP153 33..33 33 - - - 106462 RMVar_ID_106462 Human_SNP_ID_428829383 m1A Human chr10 - 37950756 37950756 37950756 GGCCCCGATTCCAGCATGGGGCATGCTACTTAATATCTCTGTGCCTCAGTTCCCATCCCATAAAA GGCCCCGATTCCAGCATGGGGCATGCTACTTATTATCTCTGTGCCTCAGTTCCCATCCCATAAAA T A ZNF25 Ensembl:ENSG00000175395 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:37950650..37950755 32194978 MeRIP-seq:(Medium) rs954254595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_377328 RMVar_hsa_circ_78915,RMVar_hsa_circ_115732,RMVar_hsa_circ_143209,RMVar_hsa_circ_143210 106463 RMVar_ID_106463 Human_SNP_ID_428829384 m1A Human chr10 - 37950756 37950756 37950756 GGCCCCGATTCCAGCATGGGGCATGCTACTTAATATCTCTGTGCCTCAGTTCCCATCCCATAAAA GGCCCCGATTCCAGCATGGGGCATGCTACTTAGTATCTCTGTGCCTCAGTTCCCATCCCATAAAA T C ZNF25 Ensembl:ENSG00000175395 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:37950650..37950755 32194978 MeRIP-seq:(Medium) rs954254595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_377328 RMVar_hsa_circ_78915,RMVar_hsa_circ_115732,RMVar_hsa_circ_143209,RMVar_hsa_circ_143210 106464 RMVar_ID_106464 Human_SNP_ID_428845183 m1A Human chr10 + 38010774 38010774 38010774 ACGCGCTTTTCTATGGCGAATGCAACCCGACGAGGGAGTGGGGTAAGCCCCAGTGGGTTGGGCAG ACGCGCTTTTCTATGGCGAATGCAACCCGACGGGGGAGTGGGGTAAGCCCCAGTGGGTTGGGCAG A G ZNF33A Ensembl:ENSG00000189180 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:38010725..38010989 26863196 MeRIP-seq:(Medium) rs1408558051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136230,Human_RBP_ID_5340427 Human_Splice_Rec_1126649,Human_Splice_Rec_1126659,Human_Splice_Rec_1126667,Human_Splice_Rec_1126673,Human_Splice_Rec_1126681,Human_Splice_Rec_1126689,Human_Splice_Rec_1126699,Human_Splice_Rec_1126705 106465 RMVar_ID_106465 Human_SNP_ID_428845216 m1A Human chr10 + 38010819 38010819 38010819 AGCCCCAGTGGGTTGGGCAGGGAGAGAGAGGGAGCCCCGCGCGACTCCTGGGGCGGGCGGCAGGG AGCCCCAGTGGGTTGGGCAGGGAGAGAGAGGGGGCCCCGCGCGACTCCTGGGGCGGGCGGCAGGG A G ZNF33A Ensembl:ENSG00000189180 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:38010810..38010971 26863196 MeRIP-seq:(Medium) rs1229451589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225986,Human_RBP_ID_27836009 106466 RMVar_ID_106466 Human_SNP_ID_428926907 m1A Human chr10 - 38349109 38349109 38349109 TCCATTGCCCCTTTTTATGTAGCCTCCTTTCTAGCCCTGACCTTCCTCCCTATTCAGTCATATGC TCCATTGCCCCTTTTTATGTAGCCTCCTTTCTCGCCCTGACCTTCCTCCCTATTCAGTCATATGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:38349058..38349151 26863196 MeRIP-seq:(Medium) rs7096961 Functional Loss SNV dbSNP153 33..33 33 - - - 106467 RMVar_ID_106467 Human_SNP_ID_428953859 m1A Human chr10 + 38450938 38450938 38450938 TCAGGCTACTGGTGGCGGGATGTGGGCCTGAGAGCTTGGTTGCAGAAACTTCGGGGTCTACAAAG TCAGGCTACTGGTGGCGGGATGTGGGCCTGAGCGCTTGGTTGCAGAAACTTCGGGGTCTACAAAG A C AL133216.2 Ensembl:ENSG00000276805 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79886842 Functional Loss SNV dbSNP153 33..33 33 - - - 106468 RMVar_ID_106468 Human_SNP_ID_428978844 m1A Human chr10 - 38507532 38507518 38507533 CCATTCTGGTCCATTCCATTCAATTCCATTCGAGTCAATTCCATTCCATTCCTTTGGAGTCCATT CCATTCTGGTCCATTCCATTCAATTCCATTC_______________CATTCCTTTGGAGTCCATT GGAATGGAATTGACTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:38507527..38507640 26863196 MeRIP-seq:(Medium) rs1564471441 Functional Loss DEL dbSNP153 32..46 33 - - - 106469 RMVar_ID_106469 Human_SNP_ID_428990973 m1A Human chr10 + 38526796 38526796 38526796 GGAATGCAATGCAATGGAATGGACTCGAATGGAATGGAATGGAATTGACTCGAATGAAATTGAAT GGAATGCAATGCAATGGAATGGACTCGAATGGCATGGAATGGAATTGACTCGAATGAAATTGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:38526793..38526898 26863196 MeRIP-seq:(Medium) rs1331606354 Functional Loss SNV dbSNP153 33..33 33 - - - 106470 RMVar_ID_106470 Human_SNP_ID_428995426 m1A Human chr10 + 38579022 38579022 38579022 AATGGAAGGGAATGGAATGGAATGGAATGGAAAGGACTGGAATGGAGTGGAATGGAATGGAACGG AATGGAAGGGAATGGAATGGAATGGAATGGAAGGGACTGGAATGGAGTGGAATGGAATGGAACGG A G lnc-ZNF37A-15 RNACentral:URS00008B7D25 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:38578968..38579102 26863196 MeRIP-seq:(Medium) rs62640615 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14562 106471 RMVar_ID_106471 Human_SNP_ID_428995427 m1A Human chr10 + 38579022 38579022 38579022 AATGGAAGGGAATGGAATGGAATGGAATGGAAAGGACTGGAATGGAGTGGAATGGAATGGAACGG AATGGAAGGGAATGGAATGGAATGGAATGGAATGGACTGGAATGGAGTGGAATGGAATGGAACGG A T lnc-ZNF37A-15 RNACentral:URS00008B7D25 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:38578968..38579102 26863196 MeRIP-seq:(Medium) rs62640615 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14562 106472 RMVar_ID_106472 Human_SNP_ID_429870167 m1A Human chr10 + 41859299 41859299 41859299 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAACGGAAAGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAACGGAATGGAATGGAATGGAACGGAAAGGAATGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41859213..41859371 26863196 MeRIP-seq:(Medium) rs201132075 Functional Loss SNV dbSNP153 33..33 33 - - - 106473 RMVar_ID_106473 Human_SNP_ID_429870168 m1A Human chr10 + 41859299 41859299 41859299 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAACGGAAAGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAACGGAAAGGAATGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41859213..41859371 26863196 MeRIP-seq:(Medium) rs201132075 Functional Loss SNV dbSNP153 33..33 33 - - - 106474 RMVar_ID_106474 Human_SNP_ID_429871649 m1A Human chr10 - 41860949 41860949 41860949 CCATTCCATTCCATTCCATTCCCTTGCATTCCACTCGGGTTGATTCCATTCCATTCCATTCCATT CCATTCCATTCCATTCCATTCCCTTGCATTCCGCTCGGGTTGATTCCATTCCATTCCATTCCATT T C HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41860900..41860984 26863196 MeRIP-seq:(Medium) rs956625704 Functional Loss SNV dbSNP153 33..33 33 - - - 106475 RMVar_ID_106475 Human_SNP_ID_429871879 m1A Human chr10 + 41861248 41861248 41861248 GAATGGAATGGAATGGAATTGAATGGAATGGAATCAACTCGAGTGGAAAGGAAAGGAATGGAAAG GAATGGAATGGAATGGAATTGAATGGAATGGATTCAACTCGAGTGGAAAGGAAAGGAATGGAAAG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41861245..41861460 26863196 MeRIP-seq:(Medium) rs796777732 Functional Loss SNV dbSNP153 33..33 33 - - - 106476 RMVar_ID_106476 Human_SNP_ID_429872557 m1A Human chr10 + 41862106 41862106 41862106 GAAAGGAAAGGAATGGAATCAACTGGAATGGAATGGAATGGAATGGAATGGAATTTAATGGAATG GAAAGGAAAGGAATGGAATCAACTGGAATGGAGTGGAATGGAATGGAATGGAATTTAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41862068..41862159 26863196 MeRIP-seq:(Medium) rs1378649038 Functional Loss SNV dbSNP153 33..33 33 - - - 106477 RMVar_ID_106477 Human_SNP_ID_429873692 m1A Human chr10 + 41863419 41863419 41863419 GGAATGGAATGGAGTGGAATAGAATCAACCCGAGTGGAATGGATTGGAATGGAGTGGAATGGAAT GGAATGGAATGGAGTGGAATAGAATCAACCCGGGTGGAATGGATTGGAATGGAGTGGAATGGAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41863300..41863549 26863196 MeRIP-seq:(Medium) rs796179908 Functional Loss SNV dbSNP153 33..33 33 - - - 106478 RMVar_ID_106478 Human_SNP_ID_429874096 m1A Human chr10 - 41863895 41863895 41863895 CTATTCCTTTCATTTCCATTCCATTTCATTCCACTCCACTCGGGTTGATTCCATTCCATTCCATT CTATTCCTTTCATTTCCATTCCATTTCATTCCCCTCCACTCGGGTTGATTCCATTCCATTCCATT T G HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41863843..41863927 26863196 MeRIP-seq:(Medium) rs796221715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17777311 106479 RMVar_ID_106479 Human_SNP_ID_429875739 m1A Human chr10 + 41865977 41865977 41865977 AATGGAATGGAATGCAGTGGAATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCA AATGGAATGGAATGCAGTGGAATGGAATCAACCCGAGTGGAATGGAATGGAACAGAATGGAATCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41865897..41866052 26863196 MeRIP-seq:(Medium) rs866274203 Functional Loss SNV dbSNP153 33..33 33 - - - 106480 RMVar_ID_106480 Human_SNP_ID_429875740 m1A Human chr10 + 41865977 41865977 41865978 AATGGAATGGAATGCAGTGGAATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCA AATGGAATGGAATGCAGTGGAATGGAATCAACCGGAGTGGAATGGAATGGAACAGAATGGAATCA AC CG - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41865897..41866052 26863196 MeRIP-seq:(Medium) rs1554802267 Functional Loss MNV dbSNP153 33..34 33 - - - 106481 RMVar_ID_106481 Human_SNP_ID_429878713 m1A Human chr10 + 41869377 41869368 41869378 GGAATGGAAGGCATTAGAATCAACTGGAATGGAAGGGAAAGAAATGAAATGGAATGGAATGGAAT GGAATGGAAGGCATTAGAATCAAC__________GGGAAAGAAATGAAATGGAATGGAATGGAAT CTGGAATGGAA C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41869364..41869540 26863196 MeRIP-seq:(Medium) rs1564448690 Functional Loss DEL dbSNP153 25..34 33 - - - 106482 RMVar_ID_106482 Human_SNP_ID_429878929 m1A Human chr10 - 41869658 41869658 41869658 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCCAGTCCATTCGGGTTGATTCCATTGCATT CCATTCCATTCCATTCCATTCCATTCCATTCCTTTCCAGTCCATTCGGGTTGATTCCATTGCATT T A HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41869616..41869738 26863196 MeRIP-seq:(Medium) rs904257900 Functional Loss SNV dbSNP153 33..33 33 - - - 106483 RMVar_ID_106483 Human_SNP_ID_429879665 m1A Human chr10 - 41870572 41870553 41870573 TGATTCCATTCCATTCCATTCCATTCCATTCCATTCCTTTCCATTCCATTCGTGTTTATTCCATT TGATTCCATTCCATTCCATTCCATTCCATTC____________________GTGTTTATTCCATT CGAATGGAATGGAAAGGAATG C HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41870423..41870616 26863196 MeRIP-seq:(Medium) rs202183229 Functional Loss DEL dbSNP153 32..51 33 - - - 106484 RMVar_ID_106484 Human_SNP_ID_429882677 m1A Human chr10 + 41874232 41874232 41874232 GGAATGGAATCAACTGGAAAGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATCAACT GGAATGGAATCAACTGGAAAGGAATGGAATGGCATGGAATGGAATGGAATGGAATGGAATCAACT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41874214..41874342 26863196 MeRIP-seq:(Medium) rs1022555197 Functional Loss SNV dbSNP153 33..33 33 - - - 106485 RMVar_ID_106485 Human_SNP_ID_429883405 m1A Human chr10 - 41875144 41875144 41875144 CCATTCCATTCCACTCGGGATGATTGCATTCCATTCCATTGCAGTCGGGTTGATTCCATTCCATT CCATTCCATTCCACTCGGGATGATTGCATTCCTTTCCATTGCAGTCGGGTTGATTCCATTCCATT T A HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41874970..41875180 26863196 MeRIP-seq:(Medium) rs367593657 Functional Loss SNV dbSNP153 33..33 33 - - - 106486 RMVar_ID_106486 Human_SNP_ID_429883952 m1A Human chr10 - 41875960 41875960 41875960 CTCCATTCCATACCCGTGCATTCCATTGCATCACATTCCTTTCCATTCCATTCCATTCCTTTCCA CTCCATTCCATACCCGTGCATTCCATTGCATCTCATTCCTTTCCATTCCATTCCATTCCTTTCCA T A HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41875943..41876072 26863196 MeRIP-seq:(Medium) rs145174067 Functional Loss SNV dbSNP153 33..33 33 - - - 106487 RMVar_ID_106487 Human_SNP_ID_429883953 m1A Human chr10 - 41875960 41875960 41875960 CTCCATTCCATACCCGTGCATTCCATTGCATCACATTCCTTTCCATTCCATTCCATTCCTTTCCA CTCCATTCCATACCCGTGCATTCCATTGCATCCCATTCCTTTCCATTCCATTCCATTCCTTTCCA T G HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41875943..41876072 26863196 MeRIP-seq:(Medium) rs145174067 Functional Loss SNV dbSNP153 33..33 33 - - - 106488 RMVar_ID_106488 Human_SNP_ID_429885485 m1A Human chr10 + 41877830 41877830 41877830 TAATGGAATGGAAAGGAATCAATCTGGGTGGAATGGAATGGAATGGAATGGAGTGGAATGGAATG TAATGGAATGGAAAGGAATCAATCTGGGTGGAGTGGAATGGAATGGAATGGAGTGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41877814..41878033 26863196 MeRIP-seq:(Medium) rs1009337766 Functional Loss SNV dbSNP153 33..33 33 - - - 106489 RMVar_ID_106489 Human_SNP_ID_429887984 m1A Human chr10 - 41880712 41880711 41880712 CCATTCCATTCCATTCCATTCCCTTCCATTCCATTCCATTCCATTGCTGTTTATTACATTCCACT CCATTCCATTCCATTCCATTCCCTTCCATTCC_TTCCATTCCATTGCTGTTTATTACATTCCACT AT A HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41880690..41880814 26863196 MeRIP-seq:(Medium) rs376146557 Functional Loss DEL dbSNP153 33..33 33 - - - 106490 RMVar_ID_106490 Human_SNP_ID_429887985 m1A Human chr10 - 41880712 41880712 41880712 CCATTCCATTCCATTCCATTCCCTTCCATTCCATTCCATTCCATTGCTGTTTATTACATTCCACT CCATTCCATTCCATTCCATTCCCTTCCATTCCCTTCCATTCCATTGCTGTTTATTACATTCCACT T G HSALNG0077440 RNACentral:URS0000EA8C54 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41880690..41880814 26863196 MeRIP-seq:(Medium) rs200919002 Functional Loss SNV dbSNP153 33..33 33 - - - 106491 RMVar_ID_106491 Human_SNP_ID_429888866 m1A Human chr10 + 41882005 41882005 41882005 CAATGGAATGGAATGGAGTGGAAGGCATTAGAATCAACTGCAATGGAATGGAATGGAATGGAATG CAATGGAATGGAATGGAGTGGAAGGCATTAGAGTCAACTGCAATGGAATGGAATGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41881661..41882075 26863196 MeRIP-seq:(Medium) rs1262220731 Functional Loss SNV dbSNP153 33..33 33 - - - 106492 RMVar_ID_106492 Human_SNP_ID_429890622 m1A Human chr10 + 41884927 41884927 41884927 GAATGGAATGGAATCAAATTGAATGGAATGGAAGGAAAGGAATGCAATGGAATGGAATCAACCTC GAATGGAATGGAATCAAATTGAATGGAATGGACGGAAAGGAATGCAATGGAATGGAATCAACCTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41884909..41885063 26863196 MeRIP-seq:(Medium) rs1174848982 Functional Loss SNV dbSNP153 33..33 33 - - - 106493 RMVar_ID_106493 Human_SNP_ID_429893531 m1A Human chr10 + 41892124 41892124 41892124 AGAATGCAATGGAATGCAATGGAATGGAATCAACCCGAGTGGAATGGAATGGAATCGAATGGAAT AGAATGCAATGGAATGCAATGGAATGGAATCATCCCGAGTGGAATGGAATGGAATCGAATGGAAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41891919..41892154 26863196 MeRIP-seq:(Medium) rs1554805502 Functional Loss SNV dbSNP153 33..33 33 - - - 106494 RMVar_ID_106494 Human_SNP_ID_429893717 m1A Human chr10 + 41892726 41892726 41892726 ACCCGAGTGCAACGGAAAGGAATGGAATGGAAAGGAATGGAATGGAATGAAATGAAGACGAGTGG ACCCGAGTGCAACGGAAAGGAATGGAATGGAACGGAATGGAATGGAATGAAATGAAGACGAGTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41892719..41892890 26863196 MeRIP-seq:(Medium) rs1267866289 Functional Loss SNV dbSNP153 33..33 33 - - - 106495 RMVar_ID_106495 Human_SNP_ID_429893718 m1A Human chr10 + 41892726 41892726 41892726 ACCCGAGTGCAACGGAAAGGAATGGAATGGAAAGGAATGGAATGGAATGAAATGAAGACGAGTGG ACCCGAGTGCAACGGAAAGGAATGGAATGGAATGGAATGGAATGGAATGAAATGAAGACGAGTGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41892719..41892890 26863196 MeRIP-seq:(Medium) rs1267866289 Functional Loss SNV dbSNP153 33..33 33 - - - 106496 RMVar_ID_106496 Human_SNP_ID_429893913 m1A Human chr10 - 41893276 41893276 41893276 CCATTCCATTCCATTCCATTCCATTCCATTCTAGTTGATTTCATTGCATTCCATGCCTTTCCATT CCATTCCATTCCATTCCATTCCATTCCATTCTTGTTGATTTCATTGCATTCCATGCCTTTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41893266..41893635 26863196 MeRIP-seq:(Medium) rs1330493754 Functional Loss SNV dbSNP153 33..33 33 - - - 106497 RMVar_ID_106497 Human_SNP_ID_429894948 m1A Human chr10 - 41895292 41895292 41895292 ATTCCATTCCATTCCATTCCATTCCATTCCATACGTGTTCATTTCATTCGATTCCATTCCATTTC ATTCCATTCCATTCCATTCCATTCCATTCCATTCGTGTTCATTTCATTCGATTCCATTCCATTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41895282..41895408 26863196 MeRIP-seq:(Medium) rs1366325061 Functional Loss SNV dbSNP153 33..33 33 - - - 106498 RMVar_ID_106498 Human_SNP_ID_429895768 m1A Human chr10 + 41897269 41897269 41897269 ATGAAATCAACCCTATTGGAATGGAATGGAATACAATGGAATGGAATGGAATGGAATTAACCCTA ATGAAATCAACCCTATTGGAATGGAATGGAATGCAATGGAATGGAATGGAATGGAATTAACCCTA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41897248..41897333 26863196 MeRIP-seq:(Medium) rs1419144976 Functional Loss SNV dbSNP153 33..33 33 - - - 106499 RMVar_ID_106499 Human_SNP_ID_429896785 m1A Human chr10 + 41899338 41899338 41899338 CCCGAGTGGAATGAAATGGAATGGAATGGAATAAACACGAGTGGAATGGAATGGAATGGAATGGA CCCGAGTGGAATGAAATGGAATGGAATGGAATCAACACGAGTGGAATGGAATGGAATGGAATGGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41899107..41899346 26863196 MeRIP-seq:(Medium) rs1369093617 Functional Loss SNV dbSNP153 33..33 33 - - - 106500 RMVar_ID_106500 Human_SNP_ID_429896786 m1A Human chr10 + 41899338 41899338 41899338 CCCGAGTGGAATGAAATGGAATGGAATGGAATAAACACGAGTGGAATGGAATGGAATGGAATGGA CCCGAGTGGAATGAAATGGAATGGAATGGAATGAACACGAGTGGAATGGAATGGAATGGAATGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41899107..41899346 26863196 MeRIP-seq:(Medium) rs1369093617 Functional Loss SNV dbSNP153 33..33 33 - - - 106501 RMVar_ID_106501 Human_SNP_ID_429896787 m1A Human chr10 + 41899338 41899338 41899338 CCCGAGTGGAATGAAATGGAATGGAATGGAATAAACACGAGTGGAATGGAATGGAATGGAATGGA CCCGAGTGGAATGAAATGGAATGGAATGGAATTAACACGAGTGGAATGGAATGGAATGGAATGGA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41899107..41899346 26863196 MeRIP-seq:(Medium) rs1369093617 Functional Loss SNV dbSNP153 33..33 33 - - - 106502 RMVar_ID_106502 Human_SNP_ID_429898835 m1A Human chr10 - 41904683 41904683 41904683 CCATTCCATAGCATTCCGTTCCATTCCATTCCATTCCAATCCTGTCCATTCCATTCCATTCCATT CCATTCCATAGCATTCCGTTCCATTCCATTCCTTTCCAATCCTGTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41904614..41904890 26863196 MeRIP-seq:(Medium) rs1474346273 Functional Loss SNV dbSNP153 33..33 33 - - - 106503 RMVar_ID_106503 Human_SNP_ID_429899846 m1A Human chr10 - 41907263 41907263 41907263 ATTTCATTCCATTCCATTTCATTCCATTCCATAGCATTCTACTCGGGTTAATTCCATTCCATTCC ATTTCATTCCATTCCATTTCATTCCATTCCATTGCATTCTACTCGGGTTAATTCCATTCCATTCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41906870..41907323 26863196 MeRIP-seq:(Medium) rs1306097285 Functional Loss SNV dbSNP153 33..33 33 - - - 106504 RMVar_ID_106504 Human_SNP_ID_429900333 m1A Human chr10 - 41908445 41908445 41908445 TTCCACTCCATTCCATTGCATTCCATGCCGTTATATTCCATTCCATTCCATTCCATTCTATACCA TTCCACTCCATTCCATTGCATTCCATGCCGTTCTATTCCATTCCATTCCATTCCATTCTATACCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41908432..41908882 26863196 MeRIP-seq:(Medium) rs1394631287 Functional Loss SNV dbSNP153 33..33 33 - - - 106505 RMVar_ID_106505 Human_SNP_ID_429902743 m1A Human chr10 + 41915811 41915811 41915811 TGCAATGGAATGCAATGATATGCAATGGAGTCAACCCTAGTGGAATGGAATGGAAAGTAATGGAA TGCAATGGAATGCAATGATATGCAATGGAGTCGACCCTAGTGGAATGGAATGGAAAGTAATGGAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41915760..41915868 26863196 MeRIP-seq:(Medium) rs1482029384 Functional Loss SNV dbSNP153 33..33 33 - - - 106506 RMVar_ID_106506 Human_SNP_ID_429902744 m1A Human chr10 + 41915811 41915811 41915811 TGCAATGGAATGCAATGATATGCAATGGAGTCAACCCTAGTGGAATGGAATGGAAAGTAATGGAA TGCAATGGAATGCAATGATATGCAATGGAGTCTACCCTAGTGGAATGGAATGGAAAGTAATGGAA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41915760..41915868 26863196 MeRIP-seq:(Medium) rs1482029384 Functional Loss SNV dbSNP153 33..33 33 - - - 106507 RMVar_ID_106507 Human_SNP_ID_430014982 m1A Human chr10 + 42312752 42312752 42312752 CCATTCCATTTGAGTCCATTCCATTCCATTCCATTCGTGTTCATTCCATTCCATTCCATTCCATT CCATTCCATTTGAGTCCATTCCATTCCATTCCGTTCGTGTTCATTCCATTCCATTCCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:42312737..42312821 26863196 MeRIP-seq:(Medium) rs1043058154 Functional Loss SNV dbSNP153 33..33 33 - - - 106508 RMVar_ID_106508 Human_SNP_ID_430014983 m1A Human chr10 + 42312752 42312752 42312752 CCATTCCATTTGAGTCCATTCCATTCCATTCCATTCGTGTTCATTCCATTCCATTCCATTCCATT CCATTCCATTTGAGTCCATTCCATTCCATTCCTTTCGTGTTCATTCCATTCCATTCCATTCCATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:42312737..42312821 26863196 MeRIP-seq:(Medium) rs1043058154 Functional Loss SNV dbSNP153 33..33 33 - - - 106509 RMVar_ID_106509 Human_SNP_ID_430073477 m1A Human chr10 + 42516683 42516683 42516683 TCAGTGGTACCAATCTCTTAACAATGCTGCCCATCTCCTCCCCCTGTCCCTTCCACACCTCACCC TCAGTGGTACCAATCTCTTAACAATGCTGCCCGTCTCCTCCCCCTGTCCCTTCCACACCTCACCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:42516626..42516743 26863196 MeRIP-seq:(Medium) rs1192268870 Functional Loss SNV dbSNP153 33..33 33 - - - 106510 RMVar_ID_106510 Human_SNP_ID_430121472 m1A Human chr10 - 42691691 42691691 42691691 CTGGAGTGGTAAGATGGCGGACGAGCAGCTGCAGCAGCTCCGTGCGGTGCTACAGGGGGAGGGGA CTGGAGTGGTAAGATGGCGGACGAGCAGCTGCCGCAGCTCCGTGCGGTGCTACAGGGGGAGGGGA T G LINC01518 Ensembl:ENSG00000233515 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr10:42691533..42691716;chr10:42691534..42691707 26863196 MeRIP-seq:(Medium) rs556306144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110955,RMVar_hsa_circ_143230 106511 RMVar_ID_106511 Human_SNP_ID_430144112 m1A Human chr10 + 42782853 42782853 42782853 CTGCGAGCAGGTTCGGTGCTGCGGGTTGGGGTAGGCGGCGGTGGGGTCCCTGGTTCTGGGGCACT CTGCGAGCAGGTTCGGTGCTGCGGGTTGGGGTGGGCGGCGGTGGGGTCCCTGGTTCTGGGGCACT A G BMS1 Ensembl:ENSG00000165733 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr10:42782840..42782933;chr10:42782839..42782974 26863196 MeRIP-seq:(Medium) rs575423644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23456486 RMVar_hsa_circ_143231,RMVar_hsa_circ_79134 106512 RMVar_ID_106512 Human_SNP_ID_430145962 m1A Human chr10 + 42790507 42790507 42790507 GCGATTAAAACACAGGTTCTGGACGGAAGTTTACCCGGTACGAAGAGAAATAATTGTTGGATACT GCGATTAAAACACAGGTTCTGGACGGAAGTTTGCCCGGTACGAAGAGAAATAATTGTTGGATACT A G BMS1 Ensembl:ENSG00000165733 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:42790458..42791673 32194978 MeRIP-seq:(Medium) rs147920722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8765289,Human_RBP_ID_24541961,Human_RBP_ID_26316208 Human_Splice_Rec_1127211 RMVar_hsa_circ_10805,RMVar_hsa_circ_105304,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_119914,RMVar_hsa_circ_273565,RMVar_hsa_circ_43537,RMVar_hsa_circ_143232,RMVar_hsa_circ_143233 106513 RMVar_ID_106513 Human_SNP_ID_430146705 m1A Human chr10 + 42793143 42793143 42793143 CTATGTTGACCTTGGTGGCAGCCACGTTTTTCAGGTATCGGTGAGACGGGAGTCATTTCTCTGAA CTATGTTGACCTTGGTGGCAGCCACGTTTTTCGGGTATCGGTGAGACGGGAGTCATTTCTCTGAA A G BMS1 Ensembl:ENSG00000165733 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:42792986..42793942 32194978 MeRIP-seq:(Medium) rs141838653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861840,Human_RBP_ID_5339153,Human_RBP_ID_8765290,Human_RBP_ID_9274113,Human_RBP_ID_19045308,Human_RBP_ID_26316214,Human_RBP_ID_26801885 Human_Splice_Rec_1127217 RMVar_hsa_circ_10805,RMVar_hsa_circ_105304,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_119914,RMVar_hsa_circ_43537,RMVar_hsa_circ_90499,RMVar_hsa_circ_143232,RMVar_hsa_circ_143233,RMVar_hsa_circ_103201,RMVar_hsa_circ_314723,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_28584,RMVar_hsa_circ_2483,RMVar_hsa_circ_143234,RMVar_hsa_circ_143236,RMVar_hsa_circ_143237,RMVar_hsa_circ_143238,RMVar_hsa_circ_143235,RMVar_hsa_circ_30730,RMVar_hsa_circ_59285,RMVar_hsa_circ_100425,RMVar_hsa_circ_143239 106514 RMVar_ID_106514 Human_SNP_ID_430147579 m1A Human chr10 - 42796588 42796588 42796588 CCGTTTTCCAACCCGTCATCTTCAGACATTTCATCATCTTCTTCATCATCACTATCTCCAGATTC CCGTTTTCCAACCCGTCATCTTCAGACATTTCGTCATCTTCTTCATCATCACTATCTCCAGATTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:42796537..42796868 26863196 MeRIP-seq:(Medium) rs1164195221 Functional Loss SNV dbSNP153 33..33 33 - - - 106515 RMVar_ID_106515 Human_SNP_ID_430147595 m1A Human chr10 - 42796627 42796627 42796627 TCAGCATTTTCCTCCTCTTCTGCTTCCTCATCACTAGAGCCGTTTTCCAACCCGTCATCTTCAGA TCAGCATTTTCCTCCTCTTCTGCTTCCTCATCGCTAGAGCCGTTTTCCAACCCGTCATCTTCAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:42796501..42796851 26863196 MeRIP-seq:(Medium) rs1331945247 Functional Loss SNV dbSNP153 33..33 33 - - - 106516 RMVar_ID_106516 Human_SNP_ID_430148180 m1A Human chr10 + 42798606 42798606 42798606 GGACTGCTCCAGATTTCTTGTGGAGGCCCCCCATGACTGGGATTTAGAGGAGGTAAGTCTGGGTA GGACTGCTCCAGATTTCTTGTGGAGGCCCCCCGTGACTGGGATTTAGAGGAGGTAAGTCTGGGTA A G BMS1 Ensembl:ENSG00000165733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:42798555..42798668 26863196 MeRIP-seq:(Medium) rs757577616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9274117,Human_RBP_ID_9360305,Human_RBP_ID_17777413,Human_RBP_ID_22886613,Human_RBP_ID_26316229,Human_RBP_ID_27802666 Human_Splice_Rec_1127225 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_43537,RMVar_hsa_circ_90499,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_28584,RMVar_hsa_circ_143234,RMVar_hsa_circ_143236,RMVar_hsa_circ_143235,RMVar_hsa_circ_30730,RMVar_hsa_circ_83308,RMVar_hsa_circ_59285,RMVar_hsa_circ_100425,RMVar_hsa_circ_143239,RMVar_hsa_circ_353251,RMVar_hsa_circ_34535,RMVar_hsa_circ_143240,RMVar_hsa_circ_143241 106517 RMVar_ID_106517 Human_SNP_ID_430149022 m1A Human chr10 + 42802201 42802201 42802201 TGGAAAGTGGGAAGATGATAAAGATGCAGCCAAGGTCTTAGCAGAAGATGGTAAGTAAAGAGCTG TGGAAAGTGGGAAGATGATAAAGATGCAGCCAGGGTCTTAGCAGAAGATGGTAAGTAAAGAGCTG A G BMS1 Ensembl:ENSG00000165733 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:42802151..42802264 26863196 MeRIP-seq:(Medium) rs1436844048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_862294,Human_RBP_ID_18410377,Human_RBP_ID_23112878,Human_RBP_ID_24542092,Human_RBP_ID_26316232 Human_Splice_Rec_1127226,Human_Splice_Rec_1127227 Human_miRNA_ID_2217788 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_90499,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_28584,RMVar_hsa_circ_143234,RMVar_hsa_circ_143236,RMVar_hsa_circ_143235,RMVar_hsa_circ_30730,RMVar_hsa_circ_83308,RMVar_hsa_circ_100425,RMVar_hsa_circ_143239,RMVar_hsa_circ_353251,RMVar_hsa_circ_143241 106518 RMVar_ID_106518 Human_SNP_ID_430149025 m1A Human chr10 - 42802217 42802217 42802217 GTCTTCCTGAAGAACCCAGCTCTTTACTTACCATCTTCTGCTAAGACCTTGGCTGCATCTTTATC GTCTTCCTGAAGAACCCAGCTCTTTACTTACCGTCTTCTGCTAAGACCTTGGCTGCATCTTTATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:42802196..42802282 26863196 MeRIP-seq:(Medium) rs1374971261 Functional Loss SNV dbSNP153 33..33 33 - - - 106519 RMVar_ID_106519 Human_SNP_ID_430151597 m1A Human chr10 + 42812699 42812699 42812699 GGACACTGCATGCCACGCAGGGTCAGATGGGCACCATACTCTGTAGTGGAGTGAGGGCTGGGGGC GGACACTGCATGCCACGCAGGGTCAGATGGGCGCCATACTCTGTAGTGGAGTGAGGGCTGGGGGC A G BMS1 Ensembl:ENSG00000165733 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:42812694..42812819 26863196 MeRIP-seq:(Medium) rs1217455765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11363554 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_90499,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_143234,RMVar_hsa_circ_143236,RMVar_hsa_circ_143235,RMVar_hsa_circ_83308,RMVar_hsa_circ_100425,RMVar_hsa_circ_143239,RMVar_hsa_circ_143241 106520 RMVar_ID_106520 Human_SNP_ID_430156168 m1A Human chr10 - 42831023 42831023 42831023 GGTTTCTTCTTTCCTTCTGCCCCTGAATTCTGAAGAGCTTCTTCCTGAGGTCCTTCTGCCGCTTC GGTTTCTTCTTTCCTTCTGCCCCTGAATTCTGGAGAGCTTCTTCCTGAGGTCCTTCTGCCGCTTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:42830973..42831058 26863196 MeRIP-seq:(Medium) rs1296279570 Functional Loss SNV dbSNP153 33..33 33 - - - 106521 RMVar_ID_106521 Human_SNP_ID_430235143 m1A Human chr10 + 43138507 43138507 43138507 GGTGGCTGAGGCGGCGGCGGGCCCAAGGCGTGAGGCGCCGCCCGGGTGTCCCCGCGGCGCAGGAG GGTGGCTGAGGCGGCGGCGGGCCCAAGGCGTGGGGCGCCGCCCGGGTGTCCCCGCGGCGCAGGAG A G CSGALNACT2 Ensembl:ENSG00000169826 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43138468..43154964 26863196 MeRIP-seq:(Medium) rs1034367423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136718,Human_RBP_ID_18416250,Human_RBP_ID_26597346 Human_Splice_Rec_1127419 106522 RMVar_ID_106522 Human_SNP_ID_430298009 m1A Human chr10 - 43386326 43386326 43386326 AAATGTGGATCTTTTACACCACATCACAGTGAACACACTGGGGAGACGTGCTTTTTTGGAAAACT AAATGTGGATCTTTTACACCACATCACAGTGAGCACACTGGGGAGACGTGCTTTTTTGGAAAACT T C HNRNPF Ensembl:ENSG00000169813 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1480389381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_377725,Human_RBP_ID_5972146,Human_RBP_ID_8988804,Human_RBP_ID_17227046,Human_RBP_ID_17343722,Human_RBP_ID_17459716,Human_RBP_ID_17777483,Human_RBP_ID_24402520,Human_RBP_ID_24456971,Human_RBP_ID_27193084,Human_RBP_ID_27607731 Human_miRNA_ID_2175128,Human_miRNA_ID_2178571,Human_miRNA_ID_2257383,Human_miRNA_ID_3035436 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275 106523 RMVar_ID_106523 Human_SNP_ID_430298104 m1A Human chr10 + 43386621 43386621 43386621 TGGCTGCCTGTGAAAATGATTGAAGTAACTCAAATGTTCCTAACAAAACTAGTCATAGCCACCCA TGGCTGCCTGTGAAAATGATTGAAGTAACTCAGATGTTCCTAACAAAACTAGTCATAGCCACCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:43386551..43386650 32194978 MeRIP-seq:(Medium) rs1425251705 Functional Loss SNV dbSNP153 33..33 33 - - - 106524 RMVar_ID_106524 Human_SNP_ID_430299206 m1A Human chr10 - 43390436 43390436 43390436 CATTGGAGGTAGGAGTCCAGGAGAAAATGGTTAGTGGATTATGGCTTCATCTCCCCTACCCGGAA CATTGGAGGTAGGAGTCCAGGAGAAAATGGTTTGTGGATTATGGCTTCATCTCCCCTACCCGGAA T A HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43390434..43390546 26863196 MeRIP-seq:(Medium) rs1350763467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11364222,Human_RBP_ID_23457273 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275 106525 RMVar_ID_106525 Human_SNP_ID_430300460 m1A Human chr10 + 43394634 43394634 43394634 AAAAGGGGCTCTTCTTAAAATAGCTTACCTTAAAAACAACCACGGATGCCTTCAGTGGGAGACAC AAAAGGGGCTCTTCTTAAAATAGCTTACCTTAGAAACAACCACGGATGCCTTCAGTGGGAGACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43394626..43394650 26863196 MeRIP-seq:(Medium) rs1020175681 Functional Loss SNV dbSNP153 33..33 33 - - - 106526 RMVar_ID_106526 Human_SNP_ID_430301110 m1A Human chr10 + 43396508 43396508 43396508 GTTTCTGTTGCTACCAGGCAAGCGCGGCTGGCAGCCAAGAGCCCCGAAATTCCACCGAAGCTCAA GTTTCTGTTGCTACCAGGCAAGCGCGGCTGGCTGCCAAGAGCCCCGAAATTCCACCGAAGCTCAA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43396407..43396546 26863196 MeRIP-seq:(Medium) rs1426020721 Functional Loss SNV dbSNP153 33..33 33 - - - 106527 RMVar_ID_106527 Human_SNP_ID_430301111 m1A Human chr10 + 43396513 43396513 43396513 TGTTGCTACCAGGCAAGCGCGGCTGGCAGCCAAGAGCCCCGAAATTCCACCGAAGCTCAACCACG TGTTGCTACCAGGCAAGCGCGGCTGGCAGCCAGGAGCCCCGAAATTCCACCGAAGCTCAACCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43396451..43396525 26863196 MeRIP-seq:(Medium) rs1034361239 Functional Loss SNV dbSNP153 33..33 33 - - - 106528 RMVar_ID_106528 Human_SNP_ID_430301116 m1A Human chr10 - 43396526 43396526 43396526 CCGGAGCCCTCTGCGTGGTTGAGCTTCGGTGGAATTTCGGGGCTCTTGGCTGCCAGCCGCGCTTG CCGGAGCCCTCTGCGTGGTTGAGCTTCGGTGGGATTTCGGGGCTCTTGGCTGCCAGCCGCGCTTG T C HNRNPF Ensembl:ENSG00000169813 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:43396501..43396525 26863196 MeRIP-seq:(Medium) rs958721663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_28033,Human_RBP_ID_377771,Human_RBP_ID_983165,Human_RBP_ID_1158857,Human_RBP_ID_1446825,Human_RBP_ID_1766867,Human_RBP_ID_3350532,Human_RBP_ID_4135822,Human_RBP_ID_5415110,Human_RBP_ID_5459277,Human_RBP_ID_5488179,Human_RBP_ID_8334624,Human_RBP_ID_8761070,Human_RBP_ID_8988817,Human_RBP_ID_16982066,Human_RBP_ID_17777527,Human_RBP_ID_18241523,Human_RBP_ID_18594142,Human_RBP_ID_22029257,Human_RBP_ID_22431401,Human_RBP_ID_22565835,Human_RBP_ID_22788161,Human_RBP_ID_26801900,Human_RBP_ID_26879142,Human_RBP_ID_27193111 Human_Splice_Rec_1127583,Human_Splice_Rec_1127588,Human_Splice_Rec_1127589,Human_Splice_Rec_1127594,Human_Splice_Rec_1127595,Human_Splice_Rec_1127600,Human_Splice_Rec_1127601,Human_Splice_Rec_1127606,Human_Splice_Rec_1127607,Human_Splice_Rec_1127612,Human_Splice_Rec_1127613,Human_Splice_Rec_1127617 Human_miRNA_ID_2438487,Human_miRNA_ID_2438488 RMVar_hsa_circ_85905,RMVar_hsa_circ_66941,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106529 RMVar_ID_106529 Human_SNP_ID_430301133 m1A Human chr10 - 43396592 43396592 43396592 AGGGACCCCACCACCACTTGGATTTCTGTTGCAGGTTGAGAACAAAAACATGCACCTGGAGTTTC AGGGACCCCACCACCACTTGGATTTCTGTTGCTGGTTGAGAACAAAAACATGCACCTGGAGTTTC T A HNRNPF Ensembl:ENSG00000169813 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:43396551..43396600 26863196 MeRIP-seq:(Medium) rs925704141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_863530,Human_RBP_ID_1446825,Human_RBP_ID_1766867,Human_RBP_ID_3350533,Human_RBP_ID_4119944,Human_RBP_ID_5972270,Human_RBP_ID_11364507,Human_RBP_ID_18594144,Human_RBP_ID_19046412,Human_RBP_ID_22536585,Human_RBP_ID_22640524,Human_RBP_ID_22735837,Human_RBP_ID_23457291,Human_RBP_ID_24812098 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106530 RMVar_ID_106530 Human_SNP_ID_430301367 m1A Human chr10 - 43396980 43396980 43396980 GCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCCACCCCACCTTGCCGTCGCCCTCGCTCTCGCCCT GCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCCCCCCCACCTTGCCGTCGCCCTCGCTCTCGCCCT T G HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43396977..43397234 26863196 MeRIP-seq:(Medium) rs1008993838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17073314,Human_RBP_ID_18476017,Human_RBP_ID_18931492 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106531 RMVar_ID_106531 Human_SNP_ID_430301379 m1A Human chr10 - 43397013 43397013 43397013 CGGCCCGCGGGTCCCCGAGCTCCCGCCTAGGCAGCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCC CGGCCCGCGGGTCCCCGAGCTCCCGCCTAGGCGGCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCC T C HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:43397007..43397200 26863196 MeRIP-seq:(Medium) rs1212607467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125868,Human_RBP_ID_5313202,Human_RBP_ID_17072979,Human_RBP_ID_18931493 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106532 RMVar_ID_106532 Human_SNP_ID_430301380 m1A Human chr10 - 43397013 43397013 43397013 CGGCCCGCGGGTCCCCGAGCTCCCGCCTAGGCAGCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCC CGGCCCGCGGGTCCCCGAGCTCCCGCCTAGGCCGCGCTAGCTTGGCGGGCCGGGGAGCAGCCCCC T G HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:43397007..43397200 26863196 MeRIP-seq:(Medium) rs1212607467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125868,Human_RBP_ID_5313202,Human_RBP_ID_17072979,Human_RBP_ID_18931493 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106533 RMVar_ID_106533 Human_SNP_ID_430304488 m1A Human chr10 - 43407511 43407509 43407512 CAACCGCAGAGTCGTGGACCAGGGTTTTGAGGAGCAAGGCACCCGACTCGCCCTCCCCCCAAGGC CAACCGCAGAGTCGTGGACCAGGGTTTTGAG___CAAGGCACCCGACTCGCCCTCCCCCCAAGGC GCTC G HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:43407496..43407743 26863196 MeRIP-seq:(Medium) rs978203020 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3363877,Human_RBP_ID_5972365,Human_RBP_ID_11364953,Human_RBP_ID_18456065,Human_RBP_ID_18476025,Human_RBP_ID_22414255,Human_RBP_ID_26775221 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 106534 RMVar_ID_106534 Human_SNP_ID_430304990 m1A Human chr10 + 43408912 43408912 43408912 AGCACGGGGCGGAGCCTACGAGGGGCGGGGTCAGGCGCGCTGCCGGCCCCAATCCTCAGCGCCTG AGCACGGGGCGGAGCCTACGAGGGGCGGGGTCCGGCGCGCTGCCGGCCCCAATCCTCAGCGCCTG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:43408902..43409125 26863196 MeRIP-seq:(Medium) rs908838032 Functional Loss SNV dbSNP153 33..33 33 - - - 106535 RMVar_ID_106535 Human_SNP_ID_430305283 m1A Human chr10 + 43409502 43409502 43409502 CCCCGCAGGACACTGAAATGTGCGCCGAAAGGACGCCTGATGGAAGACTAGGATGGGAAAAGGAA CCCCGCAGGACACTGAAATGTGCGCCGAAAGGGCGCCTGATGGAAGACTAGGATGGGAAAAGGAA A G lnc-ZNF487-4,lnc-ZNF487-4:2 RNACentral:URS0000D56E03,RNACentral:URS0000D5827C lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:43409468..43409539 26863196 MeRIP-seq:(Medium) rs954501052 Functional Loss SNV dbSNP153 33..33 33 - - - 106536 RMVar_ID_106536 Human_SNP_ID_430313327 m1A Human chr10 - 43436707 43436707 43436707 TTGAGGCCGCTGGGCGCCGCAACGTGAGCCCAAAGGACGCCCCGCTTCAAGACTGGCGCAAGAGG TTGAGGCCGCTGGGCGCCGCAACGTGAGCCCAGAGGACGCCCCGCTTCAAGACTGGCGCAAGAGG T C lnc-HNRNPF-1,lnc-HNRNPF-1:2,lnc-HNRNPF-1:3,lnc-HNRNPF-1:4,lnc-HNRNPF-1:5,lnc-HNRNPF-1:6,lnc-HNRNPF-1:7 RNACentral:URS00008C2F73,RNACentral:URS00009B40B5,RNACentral:URS0000D5A555,RNACentral:URS0000D5DFC0,RNACentral:URS0000D5A354,RNACentral:URS0000D58ECA,RNACentral:URS0000D56D5B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:43436658..43436751 26863196 MeRIP-seq:(Medium) rs1337119357 Functional Loss SNV dbSNP153 33..33 33 - - - 106537 RMVar_ID_106537 Human_SNP_ID_430316406 m1A Human chr10 + 43447112 43447112 43447112 TCGGCAGGCTGAGGCAGGAGAATCAGGCAGGGAGGTTGCAGTGAGCCGAAATCGAGGCAGTACAG TCGGCAGGCTGAGGCAGGAGAATCAGGCAGGGCGGTTGCAGTGAGCCGAAATCGAGGCAGTACAG A C ZNF487 Ensembl:ENSG00000243660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43447106..43447195 26863196 MeRIP-seq:(Medium) rs1473591770 Functional Loss SNV dbSNP153 33..33 33 - - - 106538 RMVar_ID_106538 Human_SNP_ID_430316407 m1A Human chr10 + 43447112 43447112 43447112 TCGGCAGGCTGAGGCAGGAGAATCAGGCAGGGAGGTTGCAGTGAGCCGAAATCGAGGCAGTACAG TCGGCAGGCTGAGGCAGGAGAATCAGGCAGGGGGGTTGCAGTGAGCCGAAATCGAGGCAGTACAG A G ZNF487 Ensembl:ENSG00000243660 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43447106..43447195 26863196 MeRIP-seq:(Medium) rs1473591770 Functional Loss SNV dbSNP153 33..33 33 - - - 106539 RMVar_ID_106539 Human_SNP_ID_430347867 m1A Human chr10 - 43568297 43568297 43568297 GGTGGGAATGGGGTGAAGATGACAACTCAGCAATGACACAAGAAGAGAGTGACACAGAAAGATTC GGTGGGAATGGGGTGAAGATGACAACTCAGCAGTGACACAAGAAGAGAGTGACACAGAAAGATTC T C ZNF239 Ensembl:ENSG00000196793 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43568246..43568359 26863196 MeRIP-seq:(Medium) rs1483977162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9593841 106540 RMVar_ID_106540 Human_SNP_ID_430348110 m1A Human chr10 - 43569468 43569468 43569468 GAATATGATCATAAGAGAGGCCTAGGTTGGGGAGGTGACAGGAGAGCCTCATGGGCCAGGATGAA GAATATGATCATAAGAGAGGCCTAGGTTGGGGGGGTGACAGGAGAGCCTCATGGGCCAGGATGAA T C ZNF239 Ensembl:ENSG00000196793 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43569383..43569587 26863196 MeRIP-seq:(Medium) rs1466413179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5972479,Human_RBP_ID_23457371 106541 RMVar_ID_106541 Human_SNP_ID_430348117 m1A Human chr10 + 43569501 43569501 43569501 CCCCAACCTAGGCCTCTCTTATGATCATATTCAGCACCAGTGACCCAGCAGGCCCTTGAACTGCA CCCCAACCTAGGCCTCTCTTATGATCATATTCGGCACCAGTGACCCAGCAGGCCCTTGAACTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43569366..43569571 26863196 MeRIP-seq:(Medium) rs971792495 Functional Loss SNV dbSNP153 33..33 33 - - - 106542 RMVar_ID_106542 Human_SNP_ID_430349179 m1A Human chr10 - 43574435 43574435 43574435 AGGCGCTGGGCCGCCGAGCTGCGGAAGCCGGGAGGGCGGCGATGGTAGGGCACGCGACCAGCGGA AGGCGCTGGGCCGCCGAGCTGCGGAAGCCGGGTGGGCGGCGATGGTAGGGCACGCGACCAGCGGA T A ZNF239 Ensembl:ENSG00000196793 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43574387..43574545 26863196 MeRIP-seq:(Medium) rs1564472167 Functional Loss SNV dbSNP153 33..33 33 - - - 106543 RMVar_ID_106543 Human_SNP_ID_430366217 m1A Human chr10 - 43648515 43648515 43648515 GGGCCTGAGGCGGGAGGGCAGCGTCTGCGGAGAGGAGCAGGGCCCATGGCGTCGGGGCGTGGGAG GGGCCTGAGGCGGGAGGGCAGCGTCTGCGGAGTGGAGCAGGGCCCATGGCGTCGGGGCGTGGGAG T A ZNF32 Ensembl:ENSG00000169740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:43648392..43648765 26863196 MeRIP-seq:(Medium) rs1370947569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_805438,Human_RBP_ID_23265071 RMVar_hsa_circ_108110,RMVar_hsa_circ_143282 106544 RMVar_ID_106544 Human_SNP_ID_430552688 m1A Human chr10 - 44373235 44373235 44373235 GAAGGGCCTGCCACAGCCTCCCCTGCCAGGGCAGGGCCCCAGGCATTGCCAAGGGCTTTGTTTTG GAAGGGCCTGCCACAGCCTCCCCTGCCAGGGCGGGGCCCCAGGCATTGCCAAGGGCTTTGTTTTG T C CXCL12 Ensembl:ENSG00000107562 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:44373186..44373293 32194978 MeRIP-seq:(Medium) rs911122671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_460551,Human_miRNA_ID_926184 106545 RMVar_ID_106545 Human_SNP_ID_430706279 m1A Human chr10 - 44976590 44976590 44976590 AAGTCAAGATGTCCTAAGGCCCAGGTCAGGGCATCTGGAGTCTGAAGGACCCTAGTTCCTAGAGG AAGTCAAGATGTCCTAAGGCCCAGGTCAGGGCGTCTGGAGTCTGAAGGACCCTAGTTCCTAGAGG T C DEPP1 Ensembl:ENSG00000165507 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:44976541..44976643 32194978 MeRIP-seq:(Medium) rs115775409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3090468 RMVar_hsa_circ_143286,RMVar_hsa_circ_103453 106546 RMVar_ID_106546 Human_SNP_ID_583374392 m1A Human chr15 - 75201933 75201933 75201933 GGGCCCTGCGCGGGAAGTCGCAGTGAGCACCAAGCCCGGAGCAACCCTCCTAGCTGCCGTTCGCG GGGCCCTGCGCGGGAAGTCGCAGTGAGCACCAGGCCCGGAGCAACCCTCCTAGCTGCCGTTCGCG T C lnc-RPP25-3 RNACentral:URS0000D5B49D lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:75201876..75202229 26863196 MeRIP-seq:(Medium) rs1321949236 Functional Loss SNV dbSNP153 33..33 33 - - - 106547 RMVar_ID_106547 Human_SNP_ID_583376230 m1A Human chr15 + 75208095 75208095 75208095 CCTCAGCTCCTGCTCCCACACAGCCTGCACCCACCCCCACATCTGGGCCCATTGGACTGCGGATT CCTCAGCTCCTGCTCCCACACAGCCTGCACCCCCCCCCACATCTGGGCCCATTGGACTGCGGATT A C C15orf39 Ensembl:ENSG00000167173 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:75208045..75208176 26863196 MeRIP-seq:(Medium) rs1419490213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4334034,Human_RBP_ID_8422794,Human_RBP_ID_9283729,Human_RBP_ID_17366969,Human_RBP_ID_17484557,Human_RBP_ID_27234224,Human_RBP_ID_27437058,Human_RBP_ID_27559654 106548 RMVar_ID_106548 Human_SNP_ID_583401960 m1A Human chr15 - 75321909 75321909 75321909 GAAGAAGATGAAAATGTAGAAGGAGATGACGAAGATGAAGTCAGTGAGGAGGAAGAAGAATTTGG GAAGAAGATGAAAATGTAGAAGGAGATGACGACGATGAAGTCAGTGAGGAGGAAGAAGAATTTGG T G ANP32BP1 Ensembl:ENSG00000259790 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75321870..75321969 26863196 MeRIP-seq:(Medium) rs898300190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2454251,Human_RBP_ID_3490238,Human_RBP_ID_5095814,Human_RBP_ID_18529133 106549 RMVar_ID_106549 Human_SNP_ID_583405788 m1A Human chr15 + 75336090 75336090 75336090 AAGAAATTCCCGGGCCCTGGCTTCTTGGCGCGATGGTGAGGCACTAGGGGCGAAGCGAGGCTTGG AAGAAATTCCCGGGCCCTGGCTTCTTGGCGCGGTGGTGAGGCACTAGGGGCGAAGCGAGGCTTGG A G COMMD4 Ensembl:ENSG00000140365 Protein coding start codon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:75336088..75336220 26863196 MeRIP-seq:(Medium) rs757224491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1279735,Human_RBP_ID_4342831,Human_RBP_ID_18668423,Human_RBP_ID_19067454 Human_Splice_Rec_1627821,Human_Splice_Rec_1627831,Human_Splice_Rec_1627833,Human_Splice_Rec_1627845,Human_Splice_Rec_1627859,Human_Splice_Rec_1627871,Human_Splice_Rec_1627877,Human_Splice_Rec_1627889,Human_Splice_Rec_1627893,Human_Splice_Rec_1627897,Human_Splice_Rec_1627905,Human_Splice_Rec_1627919,Human_Splice_Rec_1627933 106550 RMVar_ID_106550 Human_SNP_ID_583405793 m1A Human chr15 - 75336094 75336094 75336094 CAGCCCAAGCCTCGCTTCGCCCCTAGTGCCTCACCATCGCGCCAAGAAGCCAGGGCCCGGGAATT CAGCCCAAGCCTCGCTTCGCCCCTAGTGCCTCGCCATCGCGCCAAGAAGCCAGGGCCCGGGAATT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:75336051..75336205;chr15:75336051..75336284;chr15:75336085..75336245 26863196 MeRIP-seq:(Medium) rs1159558681 Functional Loss SNV dbSNP153 33..33 33 - - - 106551 RMVar_ID_106551 Human_SNP_ID_583405794 m1A Human chr15 - 75336094 75336094 75336094 CAGCCCAAGCCTCGCTTCGCCCCTAGTGCCTCACCATCGCGCCAAGAAGCCAGGGCCCGGGAATT CAGCCCAAGCCTCGCTTCGCCCCTAGTGCCTCCCCATCGCGCCAAGAAGCCAGGGCCCGGGAATT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:75336051..75336205;chr15:75336051..75336284;chr15:75336085..75336245 26863196 MeRIP-seq:(Medium) rs1159558681 Functional Loss SNV dbSNP153 33..33 33 - - - 106552 RMVar_ID_106552 Human_SNP_ID_583406423 m1A Human chr15 - 75338052 75338052 75338052 AGATCACCACAGAACCGGAACCTCTGCAAGGGAGGGAGGCAGGTAATCAGGCTGGAGGGAGGCCT AGATCACCACAGAACCGGAACCTCTGCAAGGGCGGGAGGCAGGTAATCAGGCTGGAGGGAGGCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:75338051..75338204;chr15:75338051..75338216;chr15:75338051..75338215 26863196 MeRIP-seq:(Medium) rs1567201378 Functional Loss SNV dbSNP153 33..33 33 - - - 106553 RMVar_ID_106553 Human_SNP_ID_583406900 m1A Human chr15 + 75339057 75339057 75339057 CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGATGGCGAATCCTTGTCCAGTGAACTGCAGCAGC CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGTTGGCGAATCCTTGTCCAGTGAACTGCAGCAGC A T COMMD4 Ensembl:ENSG00000140365 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75338631..75339180 32194978 MeRIP-seq:(Medium) rs1188436991 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_463863,Human_RBP_ID_1279738,Human_RBP_ID_4347583,Human_RBP_ID_9371144,Human_RBP_ID_12593328,Human_RBP_ID_17652370,Human_RBP_ID_18981673,Human_RBP_ID_22440422,Human_RBP_ID_26436013 Human_Splice_Rec_1627828,Human_Splice_Rec_1627829,Human_Splice_Rec_1627838,Human_Splice_Rec_1627839,Human_Splice_Rec_1627852,Human_Splice_Rec_1627853,Human_Splice_Rec_1627866,Human_Splice_Rec_1627867,Human_Splice_Rec_1627884,Human_Splice_Rec_1627885,Human_Splice_Rec_1627904,Human_Splice_Rec_1627912,Human_Splice_Rec_1627913,Human_Splice_Rec_1627926,Human_Splice_Rec_1627927,Human_Splice_Rec_1627938,Human_Splice_Rec_1627948,Human_Splice_Rec_1627949,Human_Splice_Rec_1627958,Human_Splice_Rec_1627959,Human_Splice_Rec_1627970,Human_Splice_Rec_1627971,Human_Splice_Rec_1627980,Human_Splice_Rec_1627982,Human_Splice_Rec_1627992,Human_Splice_Rec_1627993,Human_Splice_Rec_1628000,Human_Splice_Rec_1628001 Human_miRNA_ID_2875781 RMVar_hsa_circ_82878,RMVar_hsa_circ_98979,RMVar_hsa_circ_173927,RMVar_hsa_circ_173928 106554 RMVar_ID_106554 Human_SNP_ID_583406901 m1A Human chr15 + 75339057 75339057 75339057 CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGATGGCGAATCCTTGTCCAGTGAACTGCAGCAGC CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGCTGGCGAATCCTTGTCCAGTGAACTGCAGCAGC A C COMMD4 Ensembl:ENSG00000140365 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75338631..75339180 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_463863,Human_RBP_ID_1279738,Human_RBP_ID_4347583,Human_RBP_ID_9371144,Human_RBP_ID_12593328,Human_RBP_ID_17652370,Human_RBP_ID_18981673,Human_RBP_ID_22440422,Human_RBP_ID_26436013 Human_Splice_Rec_1627828,Human_Splice_Rec_1627829,Human_Splice_Rec_1627838,Human_Splice_Rec_1627839,Human_Splice_Rec_1627852,Human_Splice_Rec_1627853,Human_Splice_Rec_1627866,Human_Splice_Rec_1627867,Human_Splice_Rec_1627884,Human_Splice_Rec_1627885,Human_Splice_Rec_1627904,Human_Splice_Rec_1627912,Human_Splice_Rec_1627913,Human_Splice_Rec_1627926,Human_Splice_Rec_1627927,Human_Splice_Rec_1627938,Human_Splice_Rec_1627948,Human_Splice_Rec_1627949,Human_Splice_Rec_1627958,Human_Splice_Rec_1627959,Human_Splice_Rec_1627970,Human_Splice_Rec_1627971,Human_Splice_Rec_1627980,Human_Splice_Rec_1627982,Human_Splice_Rec_1627992,Human_Splice_Rec_1627993,Human_Splice_Rec_1628000,Human_Splice_Rec_1628001 Human_miRNA_ID_2875781 RMVar_hsa_circ_82878,RMVar_hsa_circ_98979,RMVar_hsa_circ_173927,RMVar_hsa_circ_173928 106555 RMVar_ID_106555 Human_SNP_ID_583406902 m1A Human chr15 + 75339057 75339057 75339057 CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGATGGCGAATCCTTGTCCAGTGAACTGCAGCAGC CATCCTCTCCAGTGCGGCCAAGCACAGTGTCGGTGGCGAATCCTTGTCCAGTGAACTGCAGCAGC A G COMMD4 Ensembl:ENSG00000140365 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75338631..75339180 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_463863,Human_RBP_ID_1279738,Human_RBP_ID_4347583,Human_RBP_ID_9371144,Human_RBP_ID_12593328,Human_RBP_ID_17652370,Human_RBP_ID_18981673,Human_RBP_ID_22440422,Human_RBP_ID_26436013 Human_Splice_Rec_1627828,Human_Splice_Rec_1627829,Human_Splice_Rec_1627838,Human_Splice_Rec_1627839,Human_Splice_Rec_1627852,Human_Splice_Rec_1627853,Human_Splice_Rec_1627866,Human_Splice_Rec_1627867,Human_Splice_Rec_1627884,Human_Splice_Rec_1627885,Human_Splice_Rec_1627904,Human_Splice_Rec_1627912,Human_Splice_Rec_1627913,Human_Splice_Rec_1627926,Human_Splice_Rec_1627927,Human_Splice_Rec_1627938,Human_Splice_Rec_1627948,Human_Splice_Rec_1627949,Human_Splice_Rec_1627958,Human_Splice_Rec_1627959,Human_Splice_Rec_1627970,Human_Splice_Rec_1627971,Human_Splice_Rec_1627980,Human_Splice_Rec_1627982,Human_Splice_Rec_1627992,Human_Splice_Rec_1627993,Human_Splice_Rec_1628000,Human_Splice_Rec_1628001 Human_miRNA_ID_2875781 RMVar_hsa_circ_82878,RMVar_hsa_circ_98979,RMVar_hsa_circ_173927,RMVar_hsa_circ_173928 106556 RMVar_ID_106556 Human_SNP_ID_583406914 m1A Human chr15 - 75339081 75339079 75339082 AACCCGTACCTTTGGGCAGCCCCAGCTGCTGCAGTTCACTGGACAAGGATTCGCCATCGACACTG AACCCGTACCTTTGGGCAGCCCCAGCTGCTG___TTCACTGGACAAGGATTCGCCATCGACACTG ACTG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75339033..75339114 26863196 MeRIP-seq:(Medium) rs1271629946 Functional Loss DEL dbSNP153 32..34 33 - - - 106557 RMVar_ID_106557 Human_SNP_ID_583407036 m1A Human chr15 - 75339346 75339343 75339347 AATGAGCCCGGACCCTGGCTGGCCTCATACTTACTGCGTAGGCTGCAGACCCGCAAGTGCTTCTG AATGAGCCCGGACCCTGGCTGGCCTCATACT____GCGTAGGCTGCAGACCCGCAAGTGCTTCTG CAGTA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75339279..75339380 32194978 MeRIP-seq:(Medium) rs1212900414 Functional Loss DEL dbSNP153,HGVD 32..35 33 - - - 106558 RMVar_ID_106558 Human_SNP_ID_583407173 m1A Human chr15 + 75339779 75339779 75339779 GCTCCAGCCTGCTGCAATCCGTGGAAGAGCCCATGGTGCACCTGCGGCTGGAGGTGGCAGCTGCC GCTCCAGCCTGCTGCAATCCGTGGAAGAGCCCGTGGTGCACCTGCGGCTGGAGGTGGCAGCTGCC A G COMMD4 Ensembl:ENSG00000140365 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75339701..75339850 32194978 MeRIP-seq:(Medium) rs1474380520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463866,Human_RBP_ID_4334169,Human_RBP_ID_18668429,Human_RBP_ID_22440124,Human_RBP_ID_22934672,Human_RBP_ID_27234282 Human_Splice_Rec_1627842,Human_Splice_Rec_1627843,Human_Splice_Rec_1627856,Human_Splice_Rec_1627857,Human_Splice_Rec_1627888,Human_Splice_Rec_1627916,Human_Splice_Rec_1627917,Human_Splice_Rec_1627930,Human_Splice_Rec_1627931,Human_Splice_Rec_1627952,Human_Splice_Rec_1627974,Human_Splice_Rec_1627983,Human_Splice_Rec_1627987,Human_Splice_Rec_1627996,Human_Splice_Rec_1627997,Human_Splice_Rec_1628004 RMVar_hsa_circ_82878,RMVar_hsa_circ_173928 106559 RMVar_ID_106559 Human_SNP_ID_583413474 m1A Human chr15 + 75359134 75359133 75359135 GGTCCAGCTTCACTCGGATGATGCCATTGTCCAGAGTCACGGAGCCATCAGTCTTTGTGGGAGGA GGTCCAGCTTCACTCGGATGATGCCATTGTCC__AGTCACGGAGCCATCAGTCTTTGTGGGAGGA CAG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75359070..75359171 32194978 MeRIP-seq:(Medium) rs747764059 Functional Loss DEL dbSNP153 33..34 33 - - - 106560 RMVar_ID_106560 Human_SNP_ID_583413476 m1A Human chr15 + 75359140 75359140 75359140 GCTTCACTCGGATGATGCCATTGTCCAGAGTCACGGAGCCATCAGTCTTTGTGGGAGGAGGCCTT GCTTCACTCGGATGATGCCATTGTCCAGAGTCCCGGAGCCATCAGTCTTTGTGGGAGGAGGCCTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75359089..75359211 26863196 MeRIP-seq:(Medium) rs746853573 Functional Loss SNV dbSNP153 33..33 33 - - - 106561 RMVar_ID_106561 Human_SNP_ID_583414002 m1A Human chr15 - 75360419 75360419 75360419 AGGAGAGAAGTTCAAGACCTGGGTTGGTCAAGAAAGCTTGAAGGAGGCAGAAACCCCTGAAGAAA AGGAGAGAAGTTCAAGACCTGGGTTGGTCAAGGAAGCTTGAAGGAGGCAGAAACCCCTGAAGAAA T C MAN2C1 Ensembl:ENSG00000140400 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:75360368..75360536 26863196 MeRIP-seq:(Medium) rs941227611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759002,Human_RBP_ID_5353796,Human_RBP_ID_12593690,Human_RBP_ID_21970511 RMVar_hsa_circ_86117,RMVar_hsa_circ_90887,RMVar_hsa_circ_173932,RMVar_hsa_circ_110230,RMVar_hsa_circ_173934,RMVar_hsa_circ_173935 106562 RMVar_ID_106562 Human_SNP_ID_583414097 m1A Human chr15 - 75360690 75360690 75360690 AAGGCTGGGAGACCTAGGCTTGTGGTCTCCTCAGGGTGCAGCTATCTTCTCCAAGACAGCTCTTC AAGGCTGGGAGACCTAGGCTTGTGGTCTCCTCGGGGTGCAGCTATCTTCTCCAAGACAGCTCTTC T C MAN2C1 Ensembl:ENSG00000140400 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75360662..75360763 32194978 MeRIP-seq:(Medium) rs369736781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1508661,Human_RBP_ID_23256347 RMVar_hsa_circ_86117,RMVar_hsa_circ_90887,RMVar_hsa_circ_173932,RMVar_hsa_circ_110230,RMVar_hsa_circ_173934,RMVar_hsa_circ_173935 106563 RMVar_ID_106563 Human_SNP_ID_583414330 m1A Human chr15 - 75361302 75361302 75361302 CCACTTCCCACCTGGCGACTCCTATGGGATGCAGGGCAGCGTGGAGGAGGTGAGGGGTCACCTAG CCACTTCCCACCTGGCGACTCCTATGGGATGCCGGGCAGCGTGGAGGAGGTGAGGGGTCACCTAG T G MAN2C1 Ensembl:ENSG00000140400 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75360861..75361354 32194978 MeRIP-seq:(Medium) rs1364238303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232179,Human_RBP_ID_888040,Human_RBP_ID_3945737,Human_RBP_ID_18436827,Human_RBP_ID_18981701,Human_RBP_ID_22799356,Human_RBP_ID_27809769 Human_Splice_Rec_1628188,Human_Splice_Rec_1628189,Human_Splice_Rec_1628236,Human_Splice_Rec_1628237,Human_Splice_Rec_1628280,Human_Splice_Rec_1628281,Human_Splice_Rec_1628328,Human_Splice_Rec_1628329,Human_Splice_Rec_1628427,Human_Splice_Rec_1628448,Human_Splice_Rec_1628449,Human_Splice_Rec_1628506,Human_Splice_Rec_1628507,Human_Splice_Rec_1628522,Human_Splice_Rec_1628523,Human_Splice_Rec_1628532,Human_Splice_Rec_1628533,Human_Splice_Rec_1628540,Human_Splice_Rec_1628541,Human_Splice_Rec_1628545,Human_Splice_Rec_1628552,Human_Splice_Rec_1628570 RMVar_hsa_circ_86117,RMVar_hsa_circ_110230,RMVar_hsa_circ_173934,RMVar_hsa_circ_173935,RMVar_hsa_circ_31850 106564 RMVar_ID_106564 Human_SNP_ID_583416471 m1A Human chr15 + 75368208 75368208 75368208 CAGGGCAGCTGGCCCCAAAAAGCCTGCGTGGGACGGGCCGGTGGGCACATGCTGGAGGCCGCCCC CAGGGCAGCTGGCCCCAAAAAGCCTGCGTGGGGCGGGCCGGTGGGCACATGCTGGAGGCCGCCCC A G AC068338.2 Ensembl:ENSG00000260274 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75368203..75368352 26863196 MeRIP-seq:(Medium) rs1172753522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3148093,Human_miRNA_ID_3188555 106565 RMVar_ID_106565 Human_SNP_ID_583416654 m1A Human chr15 - 75368550 75368550 75368550 TGGCGGCTGCGCCGGCCTTGAAGCACTGGCGCACCACGCTGGAGCGGGTGGAGAAGTTCGTGTCG TGGCGGCTGCGCCGGCCTTGAAGCACTGGCGCTCCACGCTGGAGCGGGTGGAGAAGTTCGTGTCG T A MAN2C1 Ensembl:ENSG00000140400 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75368460..75368591 26863196 MeRIP-seq:(Medium) rs1336026346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342833,Human_RBP_ID_18418507 Human_Splice_Rec_1628169,Human_Splice_Rec_1628217,Human_Splice_Rec_1628265,Human_Splice_Rec_1628309,Human_Splice_Rec_1628431,Human_Splice_Rec_1628493,Human_Splice_Rec_1628553,Human_Splice_Rec_1628589,Human_Splice_Rec_1628597,Human_Splice_Rec_1628609,Human_Splice_Rec_1628621,Human_Splice_Rec_1628629,Human_Splice_Rec_1628639,Human_Splice_Rec_1628647,Human_Splice_Rec_1628655 106566 RMVar_ID_106566 Human_SNP_ID_583416655 m1A Human chr15 - 75368550 75368550 75368550 TGGCGGCTGCGCCGGCCTTGAAGCACTGGCGCACCACGCTGGAGCGGGTGGAGAAGTTCGTGTCG TGGCGGCTGCGCCGGCCTTGAAGCACTGGCGCGCCACGCTGGAGCGGGTGGAGAAGTTCGTGTCG T C MAN2C1 Ensembl:ENSG00000140400 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75368460..75368591 26863196 MeRIP-seq:(Medium) rs1336026346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342833,Human_RBP_ID_18418507 Human_Splice_Rec_1628169,Human_Splice_Rec_1628217,Human_Splice_Rec_1628265,Human_Splice_Rec_1628309,Human_Splice_Rec_1628431,Human_Splice_Rec_1628493,Human_Splice_Rec_1628553,Human_Splice_Rec_1628589,Human_Splice_Rec_1628597,Human_Splice_Rec_1628609,Human_Splice_Rec_1628621,Human_Splice_Rec_1628629,Human_Splice_Rec_1628639,Human_Splice_Rec_1628647,Human_Splice_Rec_1628655 106567 RMVar_ID_106567 Human_SNP_ID_583418577 m1A Human chr15 - 75375802 75375802 75375802 AGCAGCAGGAAAAGGAAGGGAAGGAAGGAAACAGCAAGAAGACCATGGAGAATGTGGATAGTCTG AGCAGCAGGAAAAGGAAGGGAAGGAAGGAAACGGCAAGAAGACCATGGAGAATGTGGATAGTCTG T C SIN3A Ensembl:ENSG00000169375 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75375751..75375905 26863196 MeRIP-seq:(Medium) rs537899729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6464135,Human_RBP_ID_26326946 Human_Splice_Rec_1628708,Human_Splice_Rec_1628748,Human_Splice_Rec_1628788,Human_Splice_Rec_1628794 RMVar_hsa_circ_268935,RMVar_hsa_circ_348133,RMVar_hsa_circ_330989 106568 RMVar_ID_106568 Human_SNP_ID_583427727 m1A Human chr15 - 75411713 75411713 75411713 AGCCCTCCCAACTGCAAGCACATACTCCGGCCAGTCAGCAGACTCCCCCACTTCCACCGTATGCA AGCCCTCCCAACTGCAAGCACATACTCCGGCCGGTCAGCAGACTCCCCCACTTCCACCGTATGCA T C SIN3A Ensembl:ENSG00000169375 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:75411664..75411779 26863196 MeRIP-seq:(Medium) rs1322810352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886976,Human_RBP_ID_6464211,Human_RBP_ID_12594288,Human_RBP_ID_17252577,Human_RBP_ID_17367097,Human_RBP_ID_18938357 Human_Splice_Rec_1628680,Human_Splice_Rec_1628720,Human_Splice_Rec_1628760 Human_miRNA_ID_2156099,Human_miRNA_ID_2156100,Human_miRNA_ID_2159660,Human_miRNA_ID_2159661,Human_miRNA_ID_2949473,Human_miRNA_ID_2949474 RMVar_hsa_circ_37540,RMVar_hsa_circ_356305,RMVar_hsa_circ_268935,RMVar_hsa_circ_127925,RMVar_hsa_circ_173942,RMVar_hsa_circ_173943,RMVar_hsa_circ_356070,RMVar_hsa_circ_46299,RMVar_hsa_circ_51685,RMVar_hsa_circ_173946,RMVar_hsa_circ_41177,RMVar_hsa_circ_363832,RMVar_hsa_circ_51913,RMVar_hsa_circ_367788,RMVar_hsa_circ_367802,RMVar_hsa_circ_109789,RMVar_hsa_circ_289195,RMVar_hsa_circ_363008,RMVar_hsa_circ_173951,RMVar_hsa_circ_299290,RMVar_hsa_circ_359631,RMVar_hsa_circ_34476,RMVar_hsa_circ_173953,RMVar_hsa_circ_173954,RMVar_hsa_circ_32888,RMVar_hsa_circ_361143,RMVar_hsa_circ_308897,RMVar_hsa_circ_324392,RMVar_hsa_circ_64471,RMVar_hsa_circ_173958,RMVar_hsa_circ_340967,RMVar_hsa_circ_173955,RMVar_hsa_circ_173956,RMVar_hsa_circ_347212,RMVar_hsa_circ_371978,RMVar_hsa_circ_290896,RMVar_hsa_circ_173959,RMVar_hsa_circ_173961,RMVar_hsa_circ_304665,RMVar_hsa_circ_173957,RMVar_hsa_circ_295889,RMVar_hsa_circ_173960 106569 RMVar_ID_106569 Human_SNP_ID_583428034 m1A Human chr15 + 75412837 75412837 75412837 AGGAGCTGGGGCTGACTGGGCTGAAGGCTGGGAAGGATGTTGGGGTGGTGGTTGAGGCTGTGGCT AGGAGCTGGGGCTGACTGGGCTGAAGGCTGGGCAGGATGTTGGGGTGGTGGTTGAGGCTGTGGCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:75412741..75412859 26863196 MeRIP-seq:(Medium) rs1316871644 Functional Loss SNV dbSNP153 33..33 33 - - - 106570 RMVar_ID_106570 Human_SNP_ID_583439440 m1A Human chr15 + 75453374 75453374 75453374 CTAAAAATAAGTCAGACCAACGAAGCGACCCCAGGGCCAAACTGCTCGGAGGTTAGGAGGAAGCG CTAAAAATAAGTCAGACCAACGAAGCGACCCCGGGGCCAAACTGCTCGGAGGTTAGGAGGAAGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75453356..75453455 26863196 MeRIP-seq:(Medium) rs932101081 Functional Loss SNV dbSNP153 33..33 33 - - - 106571 RMVar_ID_106571 Human_SNP_ID_583443316 m1A Human chr15 - 75468539 75468539 75468539 TAGCAATGTGTTCTTAATTCCTAGCATCTGCTATCAAACTGTGCCTTATTAAAACCAAATTGTGG TAGCAATGTGTTCTTAATTCCTAGCATCTGCTGTCAAACTGTGCCTTATTAAAACCAAATTGTGG T C PTPN9 Ensembl:ENSG00000169410 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75468488..75468589 32194978 MeRIP-seq:(Medium) rs1003320133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1080270,Human_miRNA_ID_1964557,Human_miRNA_ID_2764009 RMVar_hsa_circ_119228,RMVar_hsa_circ_173966 106572 RMVar_ID_106572 Human_SNP_ID_583443380 m1A Human chr15 + 75468788 75468781 75468789 GTTCGTAGGAGAGTTACTGACTCTCCACGGCCAGCAGGTTTTGGCCAGAGGATACCATGCCCTCC GTTCGTAGGAGAGTTACTGACTCTCC________CAGGTTTTGGCCAGAGGATACCATGCCCTCC CACGGCCAG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75468688..75468789 32194978 MeRIP-seq:(Medium) rs1567458650 Functional Loss DEL dbSNP153 27..34 33 - - - 106573 RMVar_ID_106573 Human_SNP_ID_583443385 m1A Human chr15 + 75468788 75468788 75468788 GTTCGTAGGAGAGTTACTGACTCTCCACGGCCAGCAGGTTTTGGCCAGAGGATACCATGCCCTCC GTTCGTAGGAGAGTTACTGACTCTCCACGGCCGGCAGGTTTTGGCCAGAGGATACCATGCCCTCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75468688..75468789 32194978 MeRIP-seq:(Medium) rs1356314926 Functional Loss SNV dbSNP153 33..33 33 - - - 106574 RMVar_ID_106574 Human_SNP_ID_583471968 m1A Human chr15 - 75579267 75579267 75579267 GCCCGCGAGGAGCCTGGCTGAGGCAGCCGCGCAGGTCGCAGGGCCAGCGTCCGCGAGGACGGCCC GCCCGCGAGGAGCCTGGCTGAGGCAGCCGCGCGGGTCGCAGGGCCAGCGTCCGCGAGGACGGCCC T C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr15:75579176..75579287;chr15:75579112..75579295 26863196 MeRIP-seq:(Medium) rs1162629396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342835,Human_RBP_ID_26757012 106575 RMVar_ID_106575 Human_SNP_ID_583475912 m1A Human chr15 - 75595662 75595662 75595662 AAGTAGATAGATACAGGTCTGGAGGTATCAGCACATAGATGGCAGCTGAAGTCAGGTAAGAAAAA AAGTAGATAGATACAGGTCTGGAGGTATCAGCGCATAGATGGCAGCTGAAGTCAGGTAAGAAAAA T C AC105036.3 Ensembl:ENSG00000260269 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:75595626..75595765 26863196 MeRIP-seq:(Medium) rs1187436473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12595261 106576 RMVar_ID_106576 Human_SNP_ID_583482142 m1A Human chr15 - 75620991 75620991 75620991 GTAGCTTTTCTGTGTCTCAAGATCTGAACAGCACAGCTGCCCCACACCCCCGCCTATCCCAGTAC GTAGCTTTTCTGTGTCTCAAGATCTGAACAGCGCAGCTGCCCCACACCCCCGCCTATCCCAGTAC T C SNUPN Ensembl:ENSG00000169371 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr15:75620942..75621042;chr15:75620942..75622376 26863196,32194978 MeRIP-seq:(Medium) rs753845763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464004,Human_RBP_ID_3483021,Human_RBP_ID_4342836,Human_RBP_ID_26809122 Human_Splice_Rec_1628938,Human_Splice_Rec_1628939,Human_Splice_Rec_1628954,Human_Splice_Rec_1628955,Human_Splice_Rec_1628972,Human_Splice_Rec_1628973,Human_Splice_Rec_1628988,Human_Splice_Rec_1628989,Human_Splice_Rec_1629018,Human_Splice_Rec_1629019,Human_Splice_Rec_1629030,Human_Splice_Rec_1629031,Human_Splice_Rec_1629038,Human_Splice_Rec_1629039,Human_Splice_Rec_1629042,Human_Splice_Rec_1629043,Human_Splice_Rec_1629048 Human_miRNA_ID_3022071 RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173983,RMVar_hsa_circ_323168,RMVar_hsa_circ_294643,RMVar_hsa_circ_173987,RMVar_hsa_circ_173988,RMVar_hsa_circ_329643,RMVar_hsa_circ_349293,RMVar_hsa_circ_281110,RMVar_hsa_circ_359037,RMVar_hsa_circ_173990 106577 RMVar_ID_106577 Human_SNP_ID_583483265 m1A Human chr15 - 75625080 75625080 75625080 GCACCATCCAAGGAATGGGTTGAAACAGCAGGAGCCCGGCGGGGCGCAGTGGCTCACGCCTGTAA GCACCATCCAAGGAATGGGTTGAAACAGCAGGCGCCCGGCGGGGCGCAGTGGCTCACGCCTGTAA T G SNUPN Ensembl:ENSG00000169371 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:75625076..75625437 26863196 MeRIP-seq:(Medium) rs947702726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26438288 106578 RMVar_ID_106578 Human_SNP_ID_583486971 m1A Human chr15 + 75639319 75639319 75639319 AGGGCGTGGGGATTTCCAGTTTTTCCTTTTACATTACAAAGTTTCCAACACAAGAAGCCAACAAT AGGGCGTGGGGATTTCCAGTTTTTCCTTTTACGTTACAAAGTTTCCAACACAAGAAGCCAACAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75639232..75639529 32194978 MeRIP-seq:(Medium) rs968918533 Functional Loss SNV dbSNP153 33..33 33 - - - 106579 RMVar_ID_106579 Human_SNP_ID_583487371 m1A Human chr15 + 75640117 75640114 75640117 CAGGTTGTGGTCGGTGACCTCCCAGTTCAGGAAGTCCACCTGCTTCAGCAGCTTCTGCTCGTGGA CAGGTTGTGGTCGGTGACCTCCCAGTTCAG___GTCCACCTGCTTCAGCAGCTTCTGCTCGTGGA GGAA G AC105020.6 Ensembl:ENSG00000275454 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75640073..75640164 26863196 MeRIP-seq:(Medium) rs1566964482 Functional Loss DEL dbSNP153 31..33 33 - - - 106580 RMVar_ID_106580 Human_SNP_ID_583489426 m1A Human chr15 - 75647930 75647930 75647930 TCGCAGACCCTCCGCTCCGCCAGCGAGAAGGCAGCTCCAAAACAAAAAGGCGATTCCGGGAGGTG TCGCAGACCCTCCGCTCCGCCAGCGAGAAGGCGGCTCCAAAACAAAAAGGCGATTCCGGGAGGTG T C IMP3 Ensembl:ENSG00000177971 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75647882..75648027 26863196 MeRIP-seq:(Medium) rs963927427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1629053 106581 RMVar_ID_106581 Human_SNP_ID_583489480 m1A Human chr15 - 75648103 75648103 75648103 CCCCCGATCACCACCCTCGCGTGCACGCACACACTCAACAGTTTGGAGTTTGGAGAGTGAGCTCC CCCCCGATCACCACCCTCGCGTGCACGCACACGCTCAACAGTTTGGAGTTTGGAGAGTGAGCTCC T C IMP3 Ensembl:ENSG00000177971 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75647965..75648164 32194978 MeRIP-seq:(Medium) rs1190407472 Functional Loss SNV dbSNP153 33..33 33 - - - 106582 RMVar_ID_106582 Human_SNP_ID_583498884 m1A Human chr15 + 75685635 75685635 75685635 TGCCAAGGCGCCACGCGACACCATCACCAGGTAGCCGGCACTCGGTGGGCTCTTCACTGAGAATA TGCCAAGGCGCCACGCGACACCATCACCAGGTGGCCGGCACTCGGTGGGCTCTTCACTGAGAATA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75685587..75687312 32194978 MeRIP-seq:(Medium) rs767147725 Functional Loss SNV dbSNP153 33..33 33 - - - 106583 RMVar_ID_106583 Human_SNP_ID_583506082 m1A Human chr15 + 75712787 75712787 75712787 TCCCGGCGGGCTGGGCGGCAGGACTTGCGAGGAGCCAGCGGAGTCCTGGGAGCTGGGAGCTGAGT TCCCGGCGGGCTGGGCGGCAGGACTTGCGAGGGGCCAGCGGAGTCCTGGGAGCTGGGAGCTGAGT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr15:75712710..75712824;chr15:75712737..75712828 26863196 MeRIP-seq:(Medium) rs1349586596 Functional Loss SNV dbSNP153 33..33 33 - - - 106584 RMVar_ID_106584 Human_SNP_ID_583512345 m1A Human chr15 + 75738307 75738307 75738307 ACGGAGACGGCCAGTTCTGGCGGCCAGGTCCGACGCTCTAGAATCCAGCCCCATTTCCCTCCCGG ACGGAGACGGCCAGTTCTGGCGGCCAGGTCCGGCGCTCTAGAATCCAGCCCCATTTCCCTCCCGG A G AC019294.2 Ensembl:ENSG00000260288 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:75738255..75738386 26863196 MeRIP-seq:(Medium) rs773314420 Functional Loss SNV dbSNP153 33..33 33 - - - 106585 RMVar_ID_106585 Human_SNP_ID_583537683 m1A Human chr15 + 75842543 75842539 75842544 AGATAGTGACAGGTGCCCAACAAAAACTTAGCACAGGACGATGTGACACAGGGTGACTATTTGAA AGATAGTGACAGGTGCCCAACAAAAACTT_____AGGACGATGTGACACAGGGTGACTATTTGAA TAGCAC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:75842497..75842606 26863196 MeRIP-seq:(Medium) rs542946614 Functional Loss DEL dbSNP153 30..34 33 - - - 106586 RMVar_ID_106586 Human_SNP_ID_583555481 m1A Human chr15 + 75913247 75913247 75913247 TTACCACATACAGTTCTTTACATGGCTGATTCAGAAACTTTCATTAGTCTGGAAGAGTGTCGTGG TTACCACATACAGTTCTTTACATGGCTGATTCTGAAACTTTCATTAGTCTGGAAGAGTGTCGTGG A T FBXO22 Ensembl:ENSG00000167196 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:75913201..75913300 32194978 MeRIP-seq:(Medium) rs746996731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1364229,Human_RBP_ID_1508812,Human_RBP_ID_1834416,Human_RBP_ID_2454420,Human_RBP_ID_8423049,Human_RBP_ID_12596034,Human_RBP_ID_23667312 Human_Splice_Rec_1629331,Human_Splice_Rec_1629338,Human_Splice_Rec_1629339,Human_Splice_Rec_1629349,Human_Splice_Rec_1629363,Human_Splice_Rec_1629371,Human_Splice_Rec_1629377 RMVar_hsa_circ_174018,RMVar_hsa_circ_273852,RMVar_hsa_circ_326759,RMVar_hsa_circ_377209,RMVar_hsa_circ_302910,RMVar_hsa_circ_174019,RMVar_hsa_circ_174017 106587 RMVar_ID_106587 Human_SNP_ID_583622534 m1A Human chr15 - 76205780 76205780 76205780 CCAAGGTAGAGGGGAGAAAGAACAGGCTGGACAGAGGCATGGGAGGACAGCCAGAGGGGCAAGCA CCAAGGTAGAGGGGAGAAAGAACAGGCTGGACGGAGGCATGGGAGGACAGCCAGAGGGGCAAGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:76205731..76205818 26863196 MeRIP-seq:(Medium) rs1335814802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6465264 106588 RMVar_ID_106588 Human_SNP_ID_583624700 m1A Human chr15 - 76215579 76215571 76215579 GGCTTTGAACAGGCCTGCAGGAAGGCGTGGGTAGGTAGGTGAGTAGAACAAAGAGGGCTGCCCTC GGCTTTGAACAGGCCTGCAGGAAGGCGTGGGT________GAGTAGAACAAAGAGGGCTGCCCTC CACCTACCT C ETFA Ensembl:ENSG00000140374 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:76215528..76215667 26863196 MeRIP-seq:(Medium) rs1482522640 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_6465358,Human_RBP_ID_12597513 106589 RMVar_ID_106589 Human_SNP_ID_583624704 m1A Human chr15 - 76215579 76215579 76215579 GGCTTTGAACAGGCCTGCAGGAAGGCGTGGGTAGGTAGGTGAGTAGAACAAAGAGGGCTGCCCTC GGCTTTGAACAGGCCTGCAGGAAGGCGTGGGTGGGTAGGTGAGTAGAACAAAGAGGGCTGCCCTC T C ETFA Ensembl:ENSG00000140374 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:76215528..76215667 26863196 MeRIP-seq:(Medium) rs967223636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6465358,Human_RBP_ID_12597513 106590 RMVar_ID_106590 Human_SNP_ID_583624866 m1A Human chr15 - 76216343 76216343 76216343 GTGGTTCCAAACAATTATTGTTTGAACTTTTTAAATTCTGTACTAAAATCTATAATAAAGCTTTT GTGGTTCCAAACAATTATTGTTTGAACTTTTTTAATTCTGTACTAAAATCTATAATAAAGCTTTT T A ETFA Ensembl:ENSG00000140374 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1803550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113197,Human_RBP_ID_8947324,Human_RBP_ID_22194093,Human_RBP_ID_23208964,Human_RBP_ID_24412066,Human_RBP_ID_24474633,Human_RBP_ID_26438764 Clinvar_Rec_682 GWAS_ID_14563,GWAS_ID_14564,GWAS_ID_14565,GWAS_ID_14566,GWAS_ID_14567,GWAS_ID_14568 RMVar_hsa_circ_118874,RMVar_hsa_circ_122278,RMVar_hsa_circ_174026,RMVar_hsa_circ_78480,RMVar_hsa_circ_174027,RMVar_hsa_circ_174025 106591 RMVar_ID_106591 Human_SNP_ID_583643362 m1A Human chr15 - 76292472 76292472 76292472 CACCATTGATTTTGGCAACTCAGAAGCAGTTCAATTACACACACATCTGTGCTGGAGCATCTGCC CACCATTGATTTTGGCAACTCAGAAGCAGTTCCATTACACACACATCTGTGCTGGAGCATCTGCC T G ETFA Ensembl:ENSG00000140374 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1354828653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464192,Human_RBP_ID_885837,Human_RBP_ID_1508915,Human_RBP_ID_1834569,Human_RBP_ID_2455027,Human_RBP_ID_9283349,Human_RBP_ID_17251191,Human_RBP_ID_17866987,Human_RBP_ID_18981725,Human_RBP_ID_22440720 Human_Splice_Rec_1629638,Human_Splice_Rec_1629639,Human_Splice_Rec_1629658,Human_Splice_Rec_1629659,Human_Splice_Rec_1629682,Human_Splice_Rec_1629683,Human_Splice_Rec_1629708,Human_Splice_Rec_1629709,Human_Splice_Rec_1629741,Human_Splice_Rec_1629764,Human_Splice_Rec_1629765,Human_Splice_Rec_1629780,Human_Splice_Rec_1629781,Human_Splice_Rec_1629802,Human_Splice_Rec_1629803,Human_Splice_Rec_1629822,Human_Splice_Rec_1629823,Human_Splice_Rec_1629845,Human_Splice_Rec_1629856,Human_Splice_Rec_1629857,Human_Splice_Rec_1629874,Human_Splice_Rec_1629875,Human_Splice_Rec_1629890,Human_Splice_Rec_1629891,Human_Splice_Rec_1629898,Human_Splice_Rec_1629899 Human_miRNA_ID_322063 RMVar_hsa_circ_118874,RMVar_hsa_circ_174027,RMVar_hsa_circ_174029,RMVar_hsa_circ_288511,RMVar_hsa_circ_363997,RMVar_hsa_circ_324118,RMVar_hsa_circ_315717,RMVar_hsa_circ_109139,RMVar_hsa_circ_117340,RMVar_hsa_circ_311504,RMVar_hsa_circ_174031,RMVar_hsa_circ_174032,RMVar_hsa_circ_174030,RMVar_hsa_circ_299182,RMVar_hsa_circ_270918,RMVar_hsa_circ_174038,RMVar_hsa_circ_174040,RMVar_hsa_circ_174041,RMVar_hsa_circ_174039,RMVar_hsa_circ_174043,RMVar_hsa_circ_286131,RMVar_hsa_circ_307684,RMVar_hsa_circ_273528,RMVar_hsa_circ_174044,RMVar_hsa_circ_308257,RMVar_hsa_circ_174042,RMVar_hsa_circ_288219,RMVar_hsa_circ_174048,RMVar_hsa_circ_174049,RMVar_hsa_circ_119135,RMVar_hsa_circ_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_60126,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_288609,RMVar_hsa_circ_174051,RMVar_hsa_circ_278227,RMVar_hsa_circ_174054,RMVar_hsa_circ_174055,RMVar_hsa_circ_174056 106592 RMVar_ID_106592 Human_SNP_ID_583643442 m1A Human chr15 - 76292677 76292677 76292677 TAATCATAGGTGGCACAAGATCTCTGTAAAGTAGCAGGCATAGCAAAAGTTCTGGTGGCTCAGCA TAATCATAGGTGGCACAAGATCTCTGTAAAGTTGCAGGCATAGCAAAAGTTCTGGTGGCTCAGCA T A ETFA Ensembl:ENSG00000140374 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:76292626..76292725 26863196 MeRIP-seq:(Medium) rs1274661227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5178604,Human_RBP_ID_5571387,Human_RBP_ID_12598537,Human_RBP_ID_18981726,Human_RBP_ID_21888365,Human_RBP_ID_22440721,Human_RBP_ID_22650159,Human_RBP_ID_23667599,Human_RBP_ID_26809129 Human_Splice_Rec_1629636,Human_Splice_Rec_1629637,Human_Splice_Rec_1629656,Human_Splice_Rec_1629657,Human_Splice_Rec_1629762,Human_Splice_Rec_1629763,Human_Splice_Rec_1629800,Human_Splice_Rec_1629801,Human_Splice_Rec_1629820,Human_Splice_Rec_1629821,Human_Splice_Rec_1629855,Human_Splice_Rec_1629872,Human_Splice_Rec_1629873 RMVar_hsa_circ_118874,RMVar_hsa_circ_174027,RMVar_hsa_circ_174029,RMVar_hsa_circ_288511,RMVar_hsa_circ_363997,RMVar_hsa_circ_324118,RMVar_hsa_circ_315717,RMVar_hsa_circ_117340,RMVar_hsa_circ_174031,RMVar_hsa_circ_174030,RMVar_hsa_circ_299182,RMVar_hsa_circ_270918,RMVar_hsa_circ_174038,RMVar_hsa_circ_174040,RMVar_hsa_circ_174041,RMVar_hsa_circ_174039,RMVar_hsa_circ_174043,RMVar_hsa_circ_286131,RMVar_hsa_circ_273528,RMVar_hsa_circ_308257,RMVar_hsa_circ_174042,RMVar_hsa_circ_288219,RMVar_hsa_circ_174048,RMVar_hsa_circ_174049,RMVar_hsa_circ_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_288609,RMVar_hsa_circ_174051,RMVar_hsa_circ_278227,RMVar_hsa_circ_174055,RMVar_hsa_circ_174056,RMVar_hsa_circ_174058,RMVar_hsa_circ_126946,RMVar_hsa_circ_360919,RMVar_hsa_circ_174057 106593 RMVar_ID_106593 Human_SNP_ID_583643443 m1A Human chr15 - 76292677 76292677 76292677 TAATCATAGGTGGCACAAGATCTCTGTAAAGTAGCAGGCATAGCAAAAGTTCTGGTGGCTCAGCA TAATCATAGGTGGCACAAGATCTCTGTAAAGTGGCAGGCATAGCAAAAGTTCTGGTGGCTCAGCA T C ETFA Ensembl:ENSG00000140374 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:76292626..76292725 26863196 MeRIP-seq:(Medium) rs1274661227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5178604,Human_RBP_ID_5571387,Human_RBP_ID_12598537,Human_RBP_ID_18981726,Human_RBP_ID_21888365,Human_RBP_ID_22440721,Human_RBP_ID_22650159,Human_RBP_ID_23667599,Human_RBP_ID_26809129 Human_Splice_Rec_1629636,Human_Splice_Rec_1629637,Human_Splice_Rec_1629656,Human_Splice_Rec_1629657,Human_Splice_Rec_1629762,Human_Splice_Rec_1629763,Human_Splice_Rec_1629800,Human_Splice_Rec_1629801,Human_Splice_Rec_1629820,Human_Splice_Rec_1629821,Human_Splice_Rec_1629855,Human_Splice_Rec_1629872,Human_Splice_Rec_1629873 RMVar_hsa_circ_118874,RMVar_hsa_circ_174027,RMVar_hsa_circ_174029,RMVar_hsa_circ_288511,RMVar_hsa_circ_363997,RMVar_hsa_circ_324118,RMVar_hsa_circ_315717,RMVar_hsa_circ_117340,RMVar_hsa_circ_174031,RMVar_hsa_circ_174030,RMVar_hsa_circ_299182,RMVar_hsa_circ_270918,RMVar_hsa_circ_174038,RMVar_hsa_circ_174040,RMVar_hsa_circ_174041,RMVar_hsa_circ_174039,RMVar_hsa_circ_174043,RMVar_hsa_circ_286131,RMVar_hsa_circ_273528,RMVar_hsa_circ_308257,RMVar_hsa_circ_174042,RMVar_hsa_circ_288219,RMVar_hsa_circ_174048,RMVar_hsa_circ_174049,RMVar_hsa_circ_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_288609,RMVar_hsa_circ_174051,RMVar_hsa_circ_278227,RMVar_hsa_circ_174055,RMVar_hsa_circ_174056,RMVar_hsa_circ_174058,RMVar_hsa_circ_126946,RMVar_hsa_circ_360919,RMVar_hsa_circ_174057 106594 RMVar_ID_106594 Human_SNP_ID_583643453 m1A Human chr15 + 76292699 76292699 76292699 CTATGCCTGCTACTTTACAGAGATCTTGTGCCACCTATGATTAAAAGATAAGTTCCTAATTATCC CTATGCCTGCTACTTTACAGAGATCTTGTGCCCCCTATGATTAAAAGATAAGTTCCTAATTATCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:76292676..76292725 26863196 MeRIP-seq:(Medium) rs1231262303 Functional Loss SNV dbSNP153 33..33 33 - - - 106595 RMVar_ID_106595 Human_SNP_ID_583644039 m1A Human chr15 + 76295578 76295578 76295578 TGATGGAGATAATATTTGCTATGGCTGACCTTAAAAATTTCTCACCTTGTCACATTTGGTTCCAG TGATGGAGATAATATTTGCTATGGCTGACCTTTAAAATTTCTCACCTTGTCACATTTGGTTCCAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:76295576..76295750 32194978 MeRIP-seq:(Medium) rs1482792667 Functional Loss SNV dbSNP153 33..33 33 - - - 106596 RMVar_ID_106596 Human_SNP_ID_583644082 m1A Human chr15 - 76295739 76295739 76295739 CTTTACCTTTTTTTTTCCTTTTTGCTCTTTTTAGGCCTCATTGCTACGATTTCAGAGTACCCTGG CTTTACCTTTTTTTTTCCTTTTTGCTCTTTTTCGGCCTCATTGCTACGATTTCAGAGTACCCTGG T G ETFA Ensembl:ENSG00000140374 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:76295594..76309988 26863410 MeRIP-seq:(Medium) rs111279957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22799404 RMVar_hsa_circ_117340,RMVar_hsa_circ_174040,RMVar_hsa_circ_174041 106597 RMVar_ID_106597 Human_SNP_ID_583645225 m1A Human chr15 - 76300672 76300672 76300672 GTTTACCATATCCAGAGGAGGCAGAAAGCAATAGCAGTGTTTTAAGCAGGGGAGAATAACATGTT GTTTACCATATCCAGAGGAGGCAGAAAGCAATGGCAGTGTTTTAAGCAGGGGAGAATAACATGTT T C ETFA Ensembl:ENSG00000140374 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:76300670..76300835 26863196 MeRIP-seq:(Medium) rs1459974401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9808075 RMVar_hsa_circ_117340,RMVar_hsa_circ_174041 106598 RMVar_ID_106598 Human_SNP_ID_583648033 m1A Human chr15 - 76311388 76311388 76311388 GTAAGGCCGAGGTTGCGGCGGAAGCGGAGACCATGTTCCGAGCGGCGGCTCCGGGGCAGCTCCGG GTAAGGCCGAGGTTGCGGCGGAAGCGGAGACCGTGTTCCGAGCGGCGGCTCCGGGGCAGCTCCGG T C ETFA Ensembl:ENSG00000140374 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:76295637..76311475 26863196 MeRIP-seq:(Medium) rs1428896053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464202,Human_RBP_ID_758975,Human_RBP_ID_4334970,Human_RBP_ID_5316125,Human_RBP_ID_8804135,Human_RBP_ID_9324364,Human_RBP_ID_22439885 Human_Splice_Rec_1629633,Human_Splice_Rec_1629655,Human_Splice_Rec_1629679,Human_Splice_Rec_1629707,Human_Splice_Rec_1629725,Human_Splice_Rec_1629759,Human_Splice_Rec_1629779,Human_Splice_Rec_1629797,Human_Splice_Rec_1629815,Human_Splice_Rec_1629869,Human_Splice_Rec_1629885,Human_Splice_Rec_1629895 Human_miRNA_ID_3010771 RMVar_hsa_circ_117340,RMVar_hsa_circ_174041 106599 RMVar_ID_106599 Human_SNP_ID_583655077 m1A Human chr15 + 76340149 76340149 76340149 AGGCGAACAGATGGAGAGGAAGACGAACAATTAAACGAAACAAACAGAATAAAACAGAAACGAAA AGGCGAACAGATGGAGAGGAAGACGAACAATTGAACGAAACAAACAGAATAAAACAGAAACGAAA A G ISL2 Ensembl:ENSG00000159556 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:76340098..76340193 26863196 MeRIP-seq:(Medium) rs1041636257 Functional Loss SNV dbSNP153 33..33 33 - - - 106600 RMVar_ID_106600 Human_SNP_ID_583655103 m1A Human chr15 - 76340233 76340233 76340233 AGGGTGAGGCCAGAGGTTAGCGAGGGGCCGCCACCCACCCGCCCCGAGCCCAACCTCCGGGTGGC AGGGTGAGGCCAGAGGTTAGCGAGGGGCCGCCCCCCACCCGCCCCGAGCCCAACCTCCGGGTGGC T G AC027243.2 Ensembl:ENSG00000259514 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:76340139..76340253 26863196 MeRIP-seq:(Medium) rs757231186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5287860 106601 RMVar_ID_106601 Human_SNP_ID_583772771 m1A Human chr15 + 76831653 76831653 76831653 CCCCACCGCCGCACTGGTACACACTCACCCACAATGCCCCCGCACCACCACCACAGCATACTCTC CCCCACCGCCGCACTGGTACACACTCACCCACGATGCCCCCGCACCACCACCACAGCATACTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:76831631..76831699 26863196 MeRIP-seq:(Medium) rs1482409067 Functional Loss SNV dbSNP153 33..33 33 - - - 106602 RMVar_ID_106602 Human_SNP_ID_583827053 m1A Human chr15 - 77046522 77046522 77046522 AGGAGGACACGAGCCTGCTTCTGTTACCTCCAAGTGGTAACAGGACTGATGCCGAAATGTCACCA AGGAGGACACGAGCCTGCTTCTGTTACCTCCAGGTGGTAACAGGACTGATGCCGAAATGTCACCA T C TSPAN3 Ensembl:ENSG00000140391 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs996758212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464402,Human_RBP_ID_1509091,Human_RBP_ID_1834746,Human_RBP_ID_4347874,Human_RBP_ID_6466724,Human_RBP_ID_8183173,Human_RBP_ID_8423407,Human_RBP_ID_12600161,Human_RBP_ID_17366381,Human_RBP_ID_18282458,Human_RBP_ID_26436169,Human_RBP_ID_27234537 Human_miRNA_ID_1269866,Human_miRNA_ID_2479397,Human_miRNA_ID_2615813 RMVar_hsa_circ_99035,RMVar_hsa_circ_269404,RMVar_hsa_circ_174102 106603 RMVar_ID_106603 Human_SNP_ID_583827063 m1A Human chr15 - 77046554 77046552 77046555 CAATTGCGAGTCATGTAGTGTGGTAGAATTAAAGGAGGACACGAGCCTGCTTCTGTTACCTCCAA CAATTGCGAGTCATGTAGTGTGGTAGAATTA___GAGGACACGAGCCTGCTTCTGTTACCTCCAA CCTT C TSPAN3 Ensembl:ENSG00000140391 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1264162377 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_464402,Human_RBP_ID_1002193,Human_RBP_ID_1509091,Human_RBP_ID_1834746,Human_RBP_ID_3483657,Human_RBP_ID_6466725,Human_RBP_ID_8183173,Human_RBP_ID_8423408,Human_RBP_ID_9056590,Human_RBP_ID_12600167,Human_RBP_ID_17251209,Human_RBP_ID_17366381,Human_RBP_ID_17483894,Human_RBP_ID_18282458,Human_RBP_ID_18669029,Human_RBP_ID_23668096 RMVar_hsa_circ_99035,RMVar_hsa_circ_269404,RMVar_hsa_circ_174102 106604 RMVar_ID_106604 Human_SNP_ID_583827099 m1A Human chr15 - 77046696 77046696 77046696 CACTGGTGTTGGACAGAGCAGCTTGGCTTTTCATGTGCCCACCTACTTACCTACTACCTGCGACT CACTGGTGTTGGACAGAGCAGCTTGGCTTTTCGTGTGCCCACCTACTTACCTACTACCTGCGACT T C TSPAN3 Ensembl:ENSG00000140391 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:77046676..77046700 26863196 MeRIP-seq:(Medium) rs1329351079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464402,Human_RBP_ID_1834746,Human_RBP_ID_3483658,Human_RBP_ID_4347881,Human_RBP_ID_5141693,Human_RBP_ID_6466733,Human_RBP_ID_8182959,Human_RBP_ID_8423413,Human_RBP_ID_9056593,Human_RBP_ID_9808429,Human_RBP_ID_12600177,Human_RBP_ID_17251216,Human_RBP_ID_17483894,Human_RBP_ID_18512573,Human_RBP_ID_22932123,Human_RBP_ID_27234540,Human_RBP_ID_27438801 Human_miRNA_ID_2873712,Human_miRNA_ID_2981675 RMVar_hsa_circ_99035,RMVar_hsa_circ_269404,RMVar_hsa_circ_174102 106605 RMVar_ID_106605 Human_SNP_ID_583828613 m1A Human chr15 - 77052875 77052875 77052875 ACTACTCAGACTGGGAAAATACAGATTGGTTCAAAGAAACCAAAAACCAGAGTGTCCCTCTTAGC ACTACTCAGACTGGGAAAATACAGATTGGTTCGAAGAAACCAAAAACCAGAGTGTCCCTCTTAGC T C TSPAN3 Ensembl:ENSG00000140391 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:77052776..77052925 32194978 MeRIP-seq:(Medium) rs1568540311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464425,Human_RBP_ID_1509114,Human_RBP_ID_1834759,Human_RBP_ID_4335214,Human_RBP_ID_5113199,Human_RBP_ID_8423427,Human_RBP_ID_9056598,Human_RBP_ID_18669045,Human_RBP_ID_22440439,Human_RBP_ID_22758922 Human_Splice_Rec_1630718,Human_Splice_Rec_1630719,Human_Splice_Rec_1630724,Human_Splice_Rec_1630725,Human_Splice_Rec_1630734,Human_Splice_Rec_1630735,Human_Splice_Rec_1630744,Human_Splice_Rec_1630745,Human_Splice_Rec_1630756,Human_Splice_Rec_1630757,Human_Splice_Rec_1630764,Human_Splice_Rec_1630765,Human_Splice_Rec_1630776,Human_Splice_Rec_1630777 Human_miRNA_ID_2784396,Human_miRNA_ID_2784397 RMVar_hsa_circ_99035,RMVar_hsa_circ_269404,RMVar_hsa_circ_70178,RMVar_hsa_circ_174103,RMVar_hsa_circ_174102,RMVar_hsa_circ_314138,RMVar_hsa_circ_174104,RMVar_hsa_circ_276717,RMVar_hsa_circ_174105 106606 RMVar_ID_106606 Human_SNP_ID_583829057 m1A Human chr15 + 77054229 77054229 77054229 ATAGCCCGGCTAGCAGCATCAGGGTTGGTTCCATTGTAGGTCTTATACACTTTCTGAATGCTGCG ATAGCCCGGCTAGCAGCATCAGGGTTGGTTCCTTTGTAGGTCTTATACACTTTCTGAATGCTGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:77054136..77054327 26863196 MeRIP-seq:(Medium) rs114741584 Functional Loss SNV dbSNP153 33..33 33 - - - 106607 RMVar_ID_106607 Human_SNP_ID_583831715 m1A Human chr15 + 77065101 77065099 77065101 TACAGCCTGTTCCTTCAGTTCTGAATCCCCCCAGTCTCCCAATCTCTTCCAAATCACCCAAGTCA TACAGCCTGTTCCTTCAGTTCTGAATCCCCC__GTCTCCCAATCTCTTCCAAATCACCCAAGTCA CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:77065094..77065202 26863196 MeRIP-seq:(Medium) rs763275611 Functional Loss DEL dbSNP153 32..33 33 - - - 106608 RMVar_ID_106608 Human_SNP_ID_583831717 m1A Human chr15 + 77065101 77065101 77065101 TACAGCCTGTTCCTTCAGTTCTGAATCCCCCCAGTCTCCCAATCTCTTCCAAATCACCCAAGTCA TACAGCCTGTTCCTTCAGTTCTGAATCCCCCCCGTCTCCCAATCTCTTCCAAATCACCCAAGTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:77065094..77065202 26863196 MeRIP-seq:(Medium) rs895323191 Functional Loss SNV dbSNP153 33..33 33 - - - 106609 RMVar_ID_106609 Human_SNP_ID_583833366 m1A Human chr15 - 77070905 77070905 77070905 CACCTCCTCCAAGACCGTGCTGGTCTTTCTCAACCTCATCTTCTGGGTGAGCGGGGCCGGGCAGA CACCTCCTCCAAGACCGTGCTGGTCTTTCTCAGCCTCATCTTCTGGGTGAGCGGGGCCGGGCAGA T C TSPAN3 Ensembl:ENSG00000140391 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:77070876..77071000 32194978 MeRIP-seq:(Medium) rs936085475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1509178,Human_RBP_ID_4335257,Human_RBP_ID_5418772,Human_RBP_ID_5439917,Human_RBP_ID_5464286,Human_RBP_ID_5495056,Human_RBP_ID_8081285,Human_RBP_ID_9059799,Human_RBP_ID_17251225,Human_RBP_ID_17689109,Human_RBP_ID_17867170,Human_RBP_ID_19068659,Human_RBP_ID_22799434,Human_RBP_ID_23273773,Human_RBP_ID_27437345 Human_Splice_Rec_1630711,Human_Splice_Rec_1630729,Human_Splice_Rec_1630739,Human_Splice_Rec_1630761,Human_Splice_Rec_1630781,Human_Splice_Rec_1630787,Human_Splice_Rec_1630789 106610 RMVar_ID_106610 Human_SNP_ID_583833417 m1A Human chr15 - 77071001 77071001 77071001 GAGGCGCCGCCGCCATTGCCGCTCTCTCGGTGAGCGCAGCCCCGCTCTCCGGGCCGGGCCTTCGC GAGGCGCCGCCGCCATTGCCGCTCTCTCGGTGGGCGCAGCCCCGCTCTCCGGGCCGGGCCTTCGC T C TSPAN3 Ensembl:ENSG00000140391 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr15:77070857..77071152;chr15:77070876..77071125 26863196,26863410 MeRIP-seq:(Medium) rs1160990014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_464470,Human_RBP_ID_1176094,Human_RBP_ID_4335259,Human_RBP_ID_5418775,Human_RBP_ID_8423481,Human_RBP_ID_17867174,Human_RBP_ID_22440442 106611 RMVar_ID_106611 Human_SNP_ID_583833466 m1A Human chr15 - 77071078 77071078 77071078 CACTTGCTGGGGTCGGGGCTGCGCGACGGCGCAGGGGCTGCGGGGAGCGCCGCGCAGGCCGTGCA CACTTGCTGGGGTCGGGGCTGCGCGACGGCGCGGGGGCTGCGGGGAGCGCCGCGCAGGCCGTGCA T C TSPAN3 Ensembl:ENSG00000140391 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:77070876..77071150 26863196 MeRIP-seq:(Medium) rs919994380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232634,Human_RBP_ID_759549,Human_RBP_ID_4335260,Human_RBP_ID_22440133,Human_RBP_ID_22581126 Human_Splice_Rec_1630749 106612 RMVar_ID_106612 Human_SNP_ID_583884948 m1A Human chr15 + 77278459 77278459 77278459 CACATAACGCACCTATGTCCTACCACATCGCCAGCACCATGCCCAAGAGAAAGGCTGAAGGGGAT CACATAACGCACCTATGTCCTACCACATCGCCGGCACCATGCCCAAGAGAAAGGCTGAAGGGGAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:77278434..77278561 26863196 MeRIP-seq:(Medium) rs549654866 Functional Loss SNV dbSNP153 33..33 33 - - - 106613 RMVar_ID_106613 Human_SNP_ID_583917468 m1A Human chr15 + 77415743 77415743 77415743 GCTCACTGGAAAAGTGAGACTACCTTCTACTTAAGACCAACTTCTCTGCCTACGCCCTGGATCCC GCTCACTGGAAAAGTGAGACTACCTTCTACTTGAGACCAACTTCTCTGCCTACGCCCTGGATCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:77415741..77415854 26863196 MeRIP-seq:(Medium) rs1342073321 Functional Loss SNV dbSNP153 33..33 33 - - - 106614 RMVar_ID_106614 Human_SNP_ID_583918862 m1A Human chr15 + 77420797 77420796 77420797 TCTCACCGGAGCAATTGTAAATGCTATGCGGTAAGAGGAGTTACCTGTGGAAAGGTGGTTAAGAG TCTCACCGGAGCAATTGTAAATGCTATGCGGT_AGAGGAGTTACCTGTGGAAAGGTGGTTAAGAG TA T HMG20A Ensembl:ENSG00000140382 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:77420746..77420889 26863196 MeRIP-seq:(Medium) rs1320241517 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1834915 Human_Splice_Rec_1630899 106615 RMVar_ID_106615 Human_SNP_ID_583918870 m1A Human chr15 - 77420832 77420832 77420832 TTTATTTTGGTGTCCTTTCCTTTTCTTTACCTAATCTCTTAACCACCTTTCCACAGGTAACTCCT TTTATTTTGGTGTCCTTTCCTTTTCTTTACCTCATCTCTTAACCACCTTTCCACAGGTAACTCCT T G lnc-PEAK1-1,lnc-PEAK1-1:2 RNACentral:URS00009C0DCA,RNACentral:URS00008B72E3 lincRNA,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:77420782..77420921 26863196 MeRIP-seq:(Medium) rs1165766254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3483953,Human_RBP_ID_27437383 106616 RMVar_ID_106616 Human_SNP_ID_584098000 m1A Human chr15 - 78131186 78131186 78131186 ACCATGGGGAACAAGCAGACCATCTTCACCGAAGAGCAGCTAGACAACTACCAGGTGAGCTCGGC ACCATGGGGAACAAGCAGACCATCTTCACCGAGGAGCAGCTAGACAACTACCAGGTGAGCTCGGC T C CIB2 Ensembl:ENSG00000136425 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:78131175..78131300 26863196 MeRIP-seq:(Medium) rs1230526374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1631313,Human_Splice_Rec_1631323,Human_Splice_Rec_1631331,Human_Splice_Rec_1631351,Human_Splice_Rec_1631359,Human_Splice_Rec_1631367,Human_Splice_Rec_1631373,Human_Splice_Rec_1631379 106617 RMVar_ID_106617 Human_SNP_ID_584098028 m1A Human chr15 - 78131236 78131236 78131236 GCCGCTGATGGGAGTCGGAGCCCGGGCGGGCGAGCGGCGGCGCGGCGGCCACCATGGGGAACAAG GCCGCTGATGGGAGTCGGAGCCCGGGCGGGCGCGCGGCGGCGCGGCGGCCACCATGGGGAACAAG T G CIB2 Ensembl:ENSG00000136425 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr15:78131203..78131352;chr15:78131194..78131344 26863196,32194978 MeRIP-seq:(Medium) rs1567062069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342862 Human_Splice_Rec_1631313,Human_Splice_Rec_1631323,Human_Splice_Rec_1631331,Human_Splice_Rec_1631351,Human_Splice_Rec_1631359,Human_Splice_Rec_1631367,Human_Splice_Rec_1631373,Human_Splice_Rec_1631379 106618 RMVar_ID_106618 Human_SNP_ID_584098044 m1A Human chr15 - 78131261 78131261 78131261 CGGGGCGCTGGCTCCGGGTCTGGCGGCCGCTGATGGGAGTCGGAGCCCGGGCGGGCGAGCGGCGG CGGGGCGCTGGCTCCGGGTCTGGCGGCCGCTGGTGGGAGTCGGAGCCCGGGCGGGCGAGCGGCGG T C CIB2 Ensembl:ENSG00000136425 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:78131216..78131310 26863196 MeRIP-seq:(Medium) rs1456683998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342862 Human_Splice_Rec_1631313,Human_Splice_Rec_1631323,Human_Splice_Rec_1631331,Human_Splice_Rec_1631351,Human_Splice_Rec_1631359,Human_Splice_Rec_1631367,Human_Splice_Rec_1631373,Human_Splice_Rec_1631379 106619 RMVar_ID_106619 Human_SNP_ID_584102238 m1A Human chr15 - 78149427 78149427 78149427 CTGCCACACGCCGGCCTGCCAGCGCTCACCTTAGAGATCCACGCGGGCCCAGCCATCGCTTCCCC CTGCCACACGCCGGCCTGCCAGCGCTCACCTTGGAGATCCACGCGGGCCCAGCCATCGCTTCCCC T C lnc-ACSBG1-3 RNACentral:URS00008BFDDE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:78149376..78149536;chr15:78149414..78149639;chr15:78149418..78149654 26863196 MeRIP-seq:(Medium) rs11555541 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 106620 RMVar_ID_106620 Human_SNP_ID_584102241 m1A Human chr15 - 78149432 78149432 78149432 CCTGCCTGCCACACGCCGGCCTGCCAGCGCTCACCTTAGAGATCCACGCGGGCCCAGCCATCGCT CCTGCCTGCCACACGCCGGCCTGCCAGCGCTCGCCTTAGAGATCCACGCGGGCCCAGCCATCGCT T C lnc-ACSBG1-3 RNACentral:URS00008BFDDE lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:78149409..78149644 26863196 MeRIP-seq:(Medium) rs1033207881 Functional Loss SNV dbSNP153 33..33 33 - - - 106621 RMVar_ID_106621 Human_SNP_ID_584104054 m1A Human chr15 + 78157530 78157530 78157530 TTCAAAAACAAAAATTCTTACTGTCTTCTTTGATGATTTCTTATGTTCAGGTTCAGACAGTAACT TTCAAAAACAAAAATTCTTACTGTCTTCTTTGCTGATTTCTTATGTTCAGGTTCAGACAGTAACT A C IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:78157526..78157575 26863196 MeRIP-seq:(Medium) rs368699032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22650895 RMVar_hsa_circ_72086,RMVar_hsa_circ_332699,RMVar_hsa_circ_296820,RMVar_hsa_circ_65626 106622 RMVar_ID_106622 Human_SNP_ID_584104055 m1A Human chr15 + 78157530 78157530 78157530 TTCAAAAACAAAAATTCTTACTGTCTTCTTTGATGATTTCTTATGTTCAGGTTCAGACAGTAACT TTCAAAAACAAAAATTCTTACTGTCTTCTTTGGTGATTTCTTATGTTCAGGTTCAGACAGTAACT A G IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:78157526..78157575 26863196 MeRIP-seq:(Medium) rs368699032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22650895 RMVar_hsa_circ_72086,RMVar_hsa_circ_332699,RMVar_hsa_circ_296820,RMVar_hsa_circ_65626 106623 RMVar_ID_106623 Human_SNP_ID_584105281 m1A Human chr15 + 78162313 78162313 78162313 GAGCAAGCGCATTGCTGAGTTTGCCTTTGAGTATGCCCGGAACAACCACCGGAGCAACGTCACGG GAGCAAGCGCATTGCTGAGTTTGCCTTTGAGTGTGCCCGGAACAACCACCGGAGCAACGTCACGG A G IDH3A Ensembl:ENSG00000166411 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:78162223..78162375 26863196 MeRIP-seq:(Medium) rs1303775777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42475,Human_RBP_ID_232269,Human_RBP_ID_8423649,Human_RBP_ID_9056732,Human_RBP_ID_23668697 Human_Splice_Rec_1631400,Human_Splice_Rec_1631401,Human_Splice_Rec_1631418,Human_Splice_Rec_1631419,Human_Splice_Rec_1631440,Human_Splice_Rec_1631441,Human_Splice_Rec_1631466,Human_Splice_Rec_1631476,Human_Splice_Rec_1631477,Human_Splice_Rec_1631530,Human_Splice_Rec_1631538,Human_Splice_Rec_1631539,Human_Splice_Rec_1631551,Human_Splice_Rec_1631568,Human_Splice_Rec_1631569,Human_Splice_Rec_1631604,Human_Splice_Rec_1631605,Human_Splice_Rec_1631616,Human_Splice_Rec_1631617 RMVar_hsa_circ_26221,RMVar_hsa_circ_332699,RMVar_hsa_circ_296820,RMVar_hsa_circ_65626,RMVar_hsa_circ_305295,RMVar_hsa_circ_353367,RMVar_hsa_circ_174151,RMVar_hsa_circ_325525,RMVar_hsa_circ_174154,RMVar_hsa_circ_303886,RMVar_hsa_circ_174153,RMVar_hsa_circ_331170 106624 RMVar_ID_106624 Human_SNP_ID_584132238 m1A Human chr15 + 78264625 78264625 78264625 CGGCGCGGGGCGGGGGGCGGGCGGGAGCTACAAGCGGCGGCGGCGGCGGCGACCGTGACCGTGAC CGGCGCGGGGCGGGGGGCGGGCGGGAGCTACAGGCGGCGGCGGCGGCGGCGACCGTGACCGTGAC A G DNAJA4 Ensembl:ENSG00000140403 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:78264385..78264885 26863196 MeRIP-seq:(Medium) rs1567113752 Functional Loss SNV dbSNP153 33..33 33 - - - 106625 RMVar_ID_106625 Human_SNP_ID_584132264 m1A Human chr15 - 78264654 78264654 78264654 TGGCCCGCGCCCCCGCCGCCCGCTCGCGCGTCACGGTCACGGTCGCCGCCGCCGCCGCCGCTTGT TGGCCCGCGCCCCCGCCGCCCGCTCGCGCGTCCCGGTCACGGTCGCCGCCGCCGCCGCCGCTTGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:78264168..78265520 26863196 MeRIP-seq:(Medium) rs1298637775 Functional Loss SNV dbSNP153 33..33 33 - - - 106626 RMVar_ID_106626 Human_SNP_ID_584174610 m1A Human chr15 + 78438352 78438352 78438352 ATAATATGGTCTCCGGCGATGGACGCCCCAAAAGCAGGTCAGTTTCGGGCCTCCGAGCTGGGTCT ATAATATGGTCTCCGGCGATGGACGCCCCAAATGCAGGTCAGTTTCGGGCCTCCGAGCTGGGTCT A T IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:78438351..78438490 32194978 MeRIP-seq:(Medium) rs1195886910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887572 Human_Splice_Rec_1632075,Human_Splice_Rec_1632081,Human_Splice_Rec_1632123,Human_Splice_Rec_1632135,Human_Splice_Rec_1632149 Human_miRNA_ID_2360090 RMVar_hsa_circ_76692,RMVar_hsa_circ_174166 106627 RMVar_ID_106627 Human_SNP_ID_584201443 m1A Human chr15 - 78542179 78542179 78542179 GAAAATATAGTGGTCCTGGAGTCATATCTTCGAGACTGCAAAGGAAAAACACATGAGTGATTCCT GAAAATATAGTGGTCCTGGAGTCATATCTTCGGGACTGCAAAGGAAAAACACATGAGTGATTCCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:78542176..78542250 26863410 MeRIP-seq:(Medium) rs368498566 Functional Loss SNV dbSNP153 33..33 33 - - - 106628 RMVar_ID_106628 Human_SNP_ID_584201444 m1A Human chr15 - 78542179 78542179 78542179 GAAAATATAGTGGTCCTGGAGTCATATCTTCGAGACTGCAAAGGAAAAACACATGAGTGATTCCT GAAAATATAGTGGTCCTGGAGTCATATCTTCGCGACTGCAAAGGAAAAACACATGAGTGATTCCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:78542176..78542250 26863410 MeRIP-seq:(Medium) rs368498566 Functional Loss SNV dbSNP153 33..33 33 - - - 106629 RMVar_ID_106629 Human_SNP_ID_584203187 m1A Human chr15 + 78548880 78548878 78548880 AAAAGAAGTGGAGCAGTTGATCAAAAAACATGAGGAAGAAGAAGCCAAAGCTGAGCGTGAGAAGA AAAAGAAGTGGAGCAGTTGATCAAAAAACAT__GGAAGAAGAAGCCAAAGCTGAGCGTGAGAAGA TGA T PSMA4 Ensembl:ENSG00000041357 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:78548831..78548936 26863196 MeRIP-seq:(Medium) rs1567039973 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_42990,Human_RBP_ID_814538,Human_RBP_ID_1509425,Human_RBP_ID_1835240,Human_RBP_ID_2456009,Human_RBP_ID_3484335,Human_RBP_ID_5566739,Human_RBP_ID_6469054,Human_RBP_ID_8423821,Human_RBP_ID_12605648,Human_RBP_ID_22496883,Human_RBP_ID_22935390,Human_RBP_ID_23669053,Human_RBP_ID_24544125,Human_RBP_ID_26326964,Human_RBP_ID_26438787,Human_RBP_ID_27809796 Human_Splice_Rec_1632268,Human_Splice_Rec_1632284,Human_Splice_Rec_1632314,Human_Splice_Rec_1632344,Human_Splice_Rec_1632360,Human_Splice_Rec_1632372,Human_Splice_Rec_1632400,Human_Splice_Rec_1632416,Human_Splice_Rec_1632426,Human_Splice_Rec_1632456,Human_Splice_Rec_1632468 106630 RMVar_ID_106630 Human_SNP_ID_584216657 m1A Human chr15 + 78601776 78601776 78601776 CCAGCGAGGTGGAAGGGATGGTCTCAGTGATCACCAGGAGAAACACCGTCAGGGAGAGGAGGACA CCAGCGAGGTGGAAGGGATGGTCTCAGTGATCCCCAGGAGAAACACCGTCAGGGAGAGGAGGACA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:78601734..78601876 26863196 MeRIP-seq:(Medium) rs1233037687 Functional Loss SNV dbSNP153 33..33 33 - - - 106631 RMVar_ID_106631 Human_SNP_ID_584216954 m1A Human chr15 - 78602535 78602535 78602535 ACCAATCCTCTTCGGGCATTTGGGAGTCTATCAGTTTGGGACCTGTATTGTGGGATGAACTGGTG ACCAATCCTCTTCGGGCATTTGGGAGTCTATCTGTTTGGGACCTGTATTGTGGGATGAACTGGTG T A CHRNA3 Ensembl:ENSG00000080644 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:78602484..78602591 26863196 MeRIP-seq:(Medium) rs1346111110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115275,RMVar_hsa_circ_174205 106632 RMVar_ID_106632 Human_SNP_ID_584216955 m1A Human chr15 - 78602535 78602535 78602535 ACCAATCCTCTTCGGGCATTTGGGAGTCTATCAGTTTGGGACCTGTATTGTGGGATGAACTGGTG ACCAATCCTCTTCGGGCATTTGGGAGTCTATCCGTTTGGGACCTGTATTGTGGGATGAACTGGTG T G CHRNA3 Ensembl:ENSG00000080644 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:78602484..78602591 26863196 MeRIP-seq:(Medium) rs1346111110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115275,RMVar_hsa_circ_174205 106633 RMVar_ID_106633 Human_SNP_ID_584262381 m1A Human chr15 - 78776228 78776228 78776228 GCGCCTGGTCCATCTGCTCACGGAGCTGTGGCATGGGCGTACAGAGCGCCGAGCGGCAGTGCACG GCGCCTGGTCCATCTGCTCACGGAGCTGTGGCGTGGGCGTACAGAGCGCCGAGCGGCAGTGCACG T C ADAMTS7 Ensembl:ENSG00000136378 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:78774784..78776378 32194978 MeRIP-seq:(Medium) rs113644773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1632683,Human_Splice_Rec_1632741,Human_Splice_Rec_1632769 RMVar_hsa_circ_84987,RMVar_hsa_circ_113891,RMVar_hsa_circ_116429,RMVar_hsa_circ_92203,RMVar_hsa_circ_85288,RMVar_hsa_circ_174207,RMVar_hsa_circ_174209,RMVar_hsa_circ_174210,RMVar_hsa_circ_174208,RMVar_hsa_circ_92501,RMVar_hsa_circ_174206,RMVar_hsa_circ_174215 106634 RMVar_ID_106634 Human_SNP_ID_584262382 m1A Human chr15 - 78776228 78776228 78776228 GCGCCTGGTCCATCTGCTCACGGAGCTGTGGCATGGGCGTACAGAGCGCCGAGCGGCAGTGCACG GCGCCTGGTCCATCTGCTCACGGAGCTGTGGCCTGGGCGTACAGAGCGCCGAGCGGCAGTGCACG T G ADAMTS7 Ensembl:ENSG00000136378 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:78774784..78776378 32194978 MeRIP-seq:(Medium) rs113644773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1632683,Human_Splice_Rec_1632741,Human_Splice_Rec_1632769 RMVar_hsa_circ_84987,RMVar_hsa_circ_113891,RMVar_hsa_circ_116429,RMVar_hsa_circ_92203,RMVar_hsa_circ_85288,RMVar_hsa_circ_174207,RMVar_hsa_circ_174209,RMVar_hsa_circ_174210,RMVar_hsa_circ_174208,RMVar_hsa_circ_92501,RMVar_hsa_circ_174206,RMVar_hsa_circ_174215 106635 RMVar_ID_106635 Human_SNP_ID_584268698 m1A Human chr15 + 78800301 78800301 78800301 CCGGGGTGTGGGCCCGGATGTGCGCGCGGCCCAGGCCGCCGCGCCGCCGCGTCTCGCTCACAAAG CCGGGGTGTGGGCCCGGATGTGCGCGCGGCCCGGGCCGCCGCGCCGCCGCGTCTCGCTCACAAAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:78800259..78800359 32194978 MeRIP-seq:(Medium) rs762424608 Functional Loss SNV dbSNP153 33..33 33 - - - 106636 RMVar_ID_106636 Human_SNP_ID_584284683 m1A Human chr15 + 78860619 78860619 78860619 ATGGGACTCTTAATCCCAGGGTCGTGGGTTCGAGCCCCACGTTGGGCGGGTTTGTTTTGCTTTCG ATGGGACTCTTAATCCCAGGGTCGTGGGTTCGCGCCCCACGTTGGGCGGGTTTGTTTTGCTTTCG A C MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1226328177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41058,Human_RBP_ID_122500,Human_RBP_ID_232831,Human_RBP_ID_465020,Human_RBP_ID_758478,Human_RBP_ID_1176176,Human_RBP_ID_1280014,Human_RBP_ID_1509470,Human_RBP_ID_1835289,Human_RBP_ID_3484398,Human_RBP_ID_5247281,Human_RBP_ID_5274506,Human_RBP_ID_6490940,Human_RBP_ID_8251120,Human_RBP_ID_8423885,Human_RBP_ID_9056822,Human_RBP_ID_9419003,Human_RBP_ID_12606417,Human_RBP_ID_17119289,Human_RBP_ID_17484755,Human_RBP_ID_17867525,Human_RBP_ID_18207262,Human_RBP_ID_18436878,Human_RBP_ID_18545355,Human_RBP_ID_18669465,Human_RBP_ID_22799470,Human_RBP_ID_23113811,Human_RBP_ID_23127630,Human_RBP_ID_23669161,Human_RBP_ID_24531061,Human_RBP_ID_24551800,Human_RBP_ID_26748648,Human_RBP_ID_26756857,Human_RBP_ID_27155753,Human_RBP_ID_27655154 106637 RMVar_ID_106637 Human_SNP_ID_584288285 m1A Human chr15 + 78873010 78873010 78873010 GGGGTGGTGGGAGAAGGAGGAGGCGGCGAATCACTTATAAATGGCGCCGAAGCAGGACCCGAAGC GGGGTGGTGGGAGAAGGAGGAGGCGGCGAATCGCTTATAAATGGCGCCGAAGCAGGACCCGAAGC A G MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:78872826..78873782 26863196 MeRIP-seq:(Medium) rs1243739350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43484,Human_RBP_ID_232832,Human_RBP_ID_465025,Human_RBP_ID_759759,Human_RBP_ID_1002303,Human_RBP_ID_2466765,Human_RBP_ID_4336142,Human_RBP_ID_5141318,Human_RBP_ID_8230735,Human_RBP_ID_8941210,Human_RBP_ID_9056824,Human_RBP_ID_9256514,Human_RBP_ID_9283740,Human_RBP_ID_9418494,Human_RBP_ID_12606421,Human_RBP_ID_17366973,Human_RBP_ID_17651839,Human_RBP_ID_17867526,Human_RBP_ID_18418399,Human_RBP_ID_22194457,Human_RBP_ID_22799471,Human_RBP_ID_23669165,Human_RBP_ID_24474755,Human_RBP_ID_26326967,Human_RBP_ID_26935616,Human_RBP_ID_27234863 Human_Splice_Rec_1632807,Human_Splice_Rec_1632831,Human_Splice_Rec_1632851,Human_Splice_Rec_1632873,Human_Splice_Rec_1632891,Human_Splice_Rec_1632903,Human_Splice_Rec_1632917,Human_Splice_Rec_1632927,Human_Splice_Rec_1632957,Human_Splice_Rec_1632969,Human_Splice_Rec_1632987 106638 RMVar_ID_106638 Human_SNP_ID_584288331 m1A Human chr15 + 78873100 78873100 78873100 GCCTTTGGGAAAAAGGCACCTAACGGCGCAGGAGATAGAGGCGGGCTCGAGGTGATTGAGGCTTG GCCTTTGGGAAAAAGGCACCTAACGGCGCAGGCGATAGAGGCGGGCTCGAGGTGATTGAGGCTTG A C MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:78873068..78873229 32194978 MeRIP-seq:(Medium) rs961929682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12606423,Human_RBP_ID_19068686 Human_Splice_Rec_1632837 106639 RMVar_ID_106639 Human_SNP_ID_584288415 m1A Human chr15 + 78873264 78873264 78873264 AGAAAGCGCTTTGTGAAGCGAGAGTGCTGCGCAGGCGTTAGAGTGGGAGAGAGAGCGTTTGGCGC AGAAAGCGCTTTGTGAAGCGAGAGTGCTGCGCTGGCGTTAGAGTGGGAGAGAGAGCGTTTGGCGC A T MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:78873257..78873400 26863196 MeRIP-seq:(Medium) rs1276875980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6469387,Human_RBP_ID_17119291,Human_RBP_ID_23669167 106640 RMVar_ID_106640 Human_SNP_ID_584288458 m1A Human chr15 + 78873365 78873365 78873365 AGGAAGAGGGCGCGGAGAGAGCAGCCTATTGTAGGGAGGCGACGGGAGCGCCATGGCGGCGGTTA AGGAAGAGGGCGCGGAGAGAGCAGCCTATTGTGGGGAGGCGACGGGAGCGCCATGGCGGCGGTTA A G MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:78873349..78873475 26863196 MeRIP-seq:(Medium) rs144048458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17119767 106641 RMVar_ID_106641 Human_SNP_ID_584290324 m1A Human chr15 - 78878147 78878143 78878147 TCTTCTCATATATAAAAAGATTAACATCTTAGAGAGTCATCACACTTTTATTAAGGTATTCCTAG TCTTCTCATATATAAAAAGATTAACATCTTAG____TCATCACACTTTTATTAAGGTATTCCTAG ACTCT A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:78878142..78878224 26863410 MeRIP-seq:(Medium) rs1345326757 Functional Loss DEL dbSNP153 33..36 33 - - - 106642 RMVar_ID_106642 Human_SNP_ID_584290328 m1A Human chr15 - 78878147 78878147 78878147 TCTTCTCATATATAAAAAGATTAACATCTTAGAGAGTCATCACACTTTTATTAAGGTATTCCTAG TCTTCTCATATATAAAAAGATTAACATCTTAGCGAGTCATCACACTTTTATTAAGGTATTCCTAG T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr15:78878142..78878224 26863410 MeRIP-seq:(Medium) rs773120507 Functional Loss SNV dbSNP153 33..33 33 - - - 106643 RMVar_ID_106643 Human_SNP_ID_584291057 m1A Human chr15 - 78880439 78880439 78880439 TTTAAAGACACTACCTTTTCAAATCATCCTTCAAAGACACTCTACACAAGCTTTATGGTGGCCTA TTTAAAGACACTACCTTTTCAAATCATCCTTCGAAGACACTCTACACAAGCTTTATGGTGGCCTA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:78880437..78880575 26863410 MeRIP-seq:(Medium) rs1184463982 Functional Loss SNV dbSNP153 33..33 33 - - - 106644 RMVar_ID_106644 Human_SNP_ID_584292970 m1A Human chr15 - 78886128 78886128 78886128 CCGGAACCCATTCATCCCAACTGAAAAAGAGGAAAGTTAAAATTTAACTCAAAAATACTCTGTTC CCGGAACCCATTCATCCCAACTGAAAAAGAGGTAAGTTAAAATTTAACTCAAAAATACTCTGTTC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr15:78886126..78886200 26863196,32194978 MeRIP-seq:(Medium) rs1442237956 Functional Loss SNV dbSNP153 33..33 33 - - - 106645 RMVar_ID_106645 Human_SNP_ID_584294805 m1A Human chr15 - 78892225 78892225 78892225 CAGGAATCTTTACTTTAACTTCAACTCTGTTCATGAATGTTTCCTCCTAAACAGAAACAGGAGGA CAGGAATCTTTACTTTAACTTCAACTCTGTTCGTGAATGTTTCCTCCTAAACAGAAACAGGAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:78892201..78892225 26863196 MeRIP-seq:(Medium) rs763673470 Functional Loss SNV dbSNP153 33..33 33 - - - 106646 RMVar_ID_106646 Human_SNP_ID_584296307 m1A Human chr15 + 78897069 78897069 78897069 TCCTCCTGAGTACCATCGGAAAGCTGTGTGAGAGGCACTCTCACTCACTTATGTTTGGATCTCCG TCCTCCTGAGTACCATCGGAAAGCTGTGTGAGGGGCACTCTCACTCACTTATGTTTGGATCTCCG A G MORF4L1 Ensembl:ENSG00000185787 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1445971519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1632800,Human_Splice_Rec_1632830,Human_Splice_Rec_1632872,Human_Splice_Rec_1632956,Human_Splice_Rec_1632968,Human_Splice_Rec_1632986 Human_miRNA_ID_2383062,Human_miRNA_ID_2450753 RMVar_hsa_circ_126988,RMVar_hsa_circ_174220,RMVar_hsa_circ_108381,RMVar_hsa_circ_174225,RMVar_hsa_circ_88016,RMVar_hsa_circ_174228 106647 RMVar_ID_106647 Human_SNP_ID_584310682 m1A Human chr15 - 78944972 78944972 78944972 AGAGCCAAGCCGCCAGCGCTGCGATGTGGGCCACGCTGCCGCTGCTCTGCGCCGGGGCCTGGCTC AGAGCCAAGCCGCCAGCGCTGCGATGTGGGCCGCGCTGCCGCTGCTCTGCGCCGGGGCCTGGCTC T C CTSH Ensembl:ENSG00000103811 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:78944923..78945052 26863196 MeRIP-seq:(Medium) rs1399625004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342423,Human_RBP_ID_22440146 Human_Splice_Rec_1633101,Human_Splice_Rec_1633127,Human_Splice_Rec_1633151,Human_Splice_Rec_1633165,Human_Splice_Rec_1633201,Human_Splice_Rec_1633301,Human_Splice_Rec_1633313,Human_Splice_Rec_1633333 106648 RMVar_ID_106648 Human_SNP_ID_584402858 m1A Human chr15 - 79322226 79322225 79322226 GCTCCAGCCTGGGGCATGAGGGGCCCTAGAGCAGGATGCCGGGGCTAGGAGTGGACTGCCCTGCT GCTCCAGCCTGGGGCATGAGGGGCCCTAGAGC_GGATGCCGGGGCTAGGAGTGGACTGCCCTGCT CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:79322176..79322325 32194978 MeRIP-seq:(Medium) rs901094658 Functional Loss DEL dbSNP153 33..33 33 - - - 106649 RMVar_ID_106649 Human_SNP_ID_584402859 m1A Human chr15 - 79322226 79322226 79322226 GCTCCAGCCTGGGGCATGAGGGGCCCTAGAGCAGGATGCCGGGGCTAGGAGTGGACTGCCCTGCT GCTCCAGCCTGGGGCATGAGGGGCCCTAGAGCGGGATGCCGGGGCTAGGAGTGGACTGCCCTGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:79322176..79322325 32194978 MeRIP-seq:(Medium) rs1379961200 Functional Loss SNV dbSNP153 33..33 33 - - - 106650 RMVar_ID_106650 Human_SNP_ID_584402919 m1A Human chr15 + 79322452 79322452 79322452 ATTAAGTGTGCAGCGCTGAAAAGACATTTACAACTAGGCCAGGGATTAGCCACTGTGGGAGGGTG ATTAAGTGTGCAGCGCTGAAAAGACATTTACAGCTAGGCCAGGGATTAGCCACTGTGGGAGGGTG A G TMED3 Ensembl:ENSG00000166557 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:79322402..79322529 26863196 MeRIP-seq:(Medium) rs1470206150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42484,Human_RBP_ID_465110,Human_RBP_ID_1176204,Human_RBP_ID_3484495,Human_RBP_ID_5113071,Human_RBP_ID_6469814,Human_RBP_ID_8423963,Human_RBP_ID_17251326,Human_RBP_ID_17652395,Human_RBP_ID_17867569,Human_RBP_ID_27234907,Human_RBP_ID_27437516 Human_miRNA_ID_2228805 RMVar_hsa_circ_78012,RMVar_hsa_circ_174237 106651 RMVar_ID_106651 Human_SNP_ID_584423915 m1A Human chr15 + 79411536 79411536 79411536 ACAGATTTTCAGCGGGGAGGCACTGAGAGTGGATGGAGGGAAGACACAGAAGCTACGCTGAAGTG ACAGATTTTCAGCGGGGAGGCACTGAGAGTGGCTGGAGGGAAGACACAGAAGCTACGCTGAAGTG A C TMED3 Ensembl:ENSG00000166557 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:79411485..79411649 26863196 MeRIP-seq:(Medium) rs898400935 Functional Loss SNV dbSNP153 33..33 33 - - - 106652 RMVar_ID_106652 Human_SNP_ID_584423916 m1A Human chr15 + 79411536 79411536 79411536 ACAGATTTTCAGCGGGGAGGCACTGAGAGTGGATGGAGGGAAGACACAGAAGCTACGCTGAAGTG ACAGATTTTCAGCGGGGAGGCACTGAGAGTGGGTGGAGGGAAGACACAGAAGCTACGCTGAAGTG A G TMED3 Ensembl:ENSG00000166557 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:79411485..79411649 26863196 MeRIP-seq:(Medium) rs898400935 Functional Loss SNV dbSNP153 33..33 33 - - - 106653 RMVar_ID_106653 Human_SNP_ID_584431041 m1A Human chr15 - 79439493 79439489 79439493 TCCCACACAACACAGAGAACATTCCCTGACTGACTGCCACCATATCCCACATACTCATGGCCTAC TCCCACACAACACAGAGAACATTCCCTGACTG____CCACCATATCCCACATACTCATGGCCTAC GCAGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:79439370..79439617 26863196 MeRIP-seq:(Medium) rs930409960 Functional Loss DEL dbSNP153 33..36 33 - - - 106654 RMVar_ID_106654 Human_SNP_ID_584433849 m1A Human chr15 - 79452049 79452047 79452049 ACAAACACATTCACACCTCTGCACACACACACATTCACAAACACGTATACACCACATACACAGGC ACAAACACATTCACACCTCTGCACACACACAC__TCACAAACACGTATACACCACATACACAGGC AAT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:79452000..79452296 26863196 MeRIP-seq:(Medium) rs1491349873 Functional Loss DEL dbSNP153 33..34 33 - - - 106655 RMVar_ID_106655 Human_SNP_ID_584433990 m1A Human chr15 - 79452441 79452441 79452441 CTTCACACCCAGACTCACACCCACACACACTCACACAGACTCACCCACACACTCATACAGCTTCA CTTCACACCCAGACTCACACCCACACACACTCGCACAGACTCACCCACACACTCATACAGCTTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:79452015..79452931 26863196 MeRIP-seq:(Medium) rs897729710 Functional Loss SNV dbSNP153 33..33 33 - - - 106656 RMVar_ID_106656 Human_SNP_ID_584434274 m1A Human chr15 - 79452800 79452798 79452800 ACACTGACAGCTTCACACCCACAGAGCTTCACACTTAGACTCACCTAGACACAGACACGCACACA ACACTGACAGCTTCACACCCACAGAGCTTCAC__TTAGACTCACCTAGACACAGACACGCACACA AGT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:79452733..79452907 26863196 MeRIP-seq:(Medium) rs1320351692 Functional Loss DEL dbSNP153 33..34 33 - - - 106657 RMVar_ID_106657 Human_SNP_ID_584508331 m1A Human chr15 + 79744711 79744711 79744711 CATTTGACTGCAGATCAAGAGGTCCCCGGTTCAAATCCGGGTGCCCCCTGCCTGAAAGTTTTCTT CATTTGACTGCAGATCAAGAGGTCCCCGGTTCCAATCCGGGTGCCCCCTGCCTGAAAGTTTTCTT A C tRNA-Cys-GCA-5-1,tRNA-Cys-GCA-2-2,tRNA-Cys-GCA-8-1 RNACentral:URS00006A14B6,RNACentral:URS0000417A0F,RNACentral:URS000042C3BF tRNA,tRNA,tRNA exon,exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs899915149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465164,Human_RBP_ID_8424015,Human_RBP_ID_20068020,Human_RBP_ID_22799817,Human_RBP_ID_23127639,Human_RBP_ID_23669472 106658 RMVar_ID_106658 Human_SNP_ID_584545693 m1A Human chr15 - 79896967 79896967 79896967 TTGGGCGTGAGATGGCGGCGGCAGCGGTGAGCAGCGCCAAGCGGAGCCTGCGGGGAGAGCTGAAG TTGGGCGTGAGATGGCGGCGGCAGCGGTGAGCGGCGCCAAGCGGAGCCTGCGGGGAGAGCTGAAG T C ST20-MTHFS,MTHFS Ensembl:ENSG00000259332,Ensembl:ENSG00000136371 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:79896870..79897016;chr15:79889201..79907663;chr15:79889252..79907663;chr15:79889203..79897025 26863196 MeRIP-seq:(Medium) rs1030708924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342884,Human_RBP_ID_5113210,Human_RBP_ID_5316313,Human_RBP_ID_8941241,Human_RBP_ID_17652056,Human_RBP_ID_18418515,Human_RBP_ID_18982529,Human_RBP_ID_27809800 Human_Splice_Rec_1633631 RMVar_hsa_circ_80592,RMVar_hsa_circ_174246 106659 RMVar_ID_106659 Human_SNP_ID_584552543 m1A Human chr15 - 79922806 79922806 79922806 ACTGCTTTGTAGGCAGGGATTCTGCTTTGTATAGGAGACCAGCTTTCGGATGCTGGTCTGGGCAT ACTGCTTTGTAGGCAGGGATTCTGCTTTGTATTGGAGACCAGCTTTCGGATGCTGGTCTGGGCAT T A ST20-MTHFS,ST20 Ensembl:ENSG00000259332,Ensembl:ENSG00000180953 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:79922794..79922922 26863196 MeRIP-seq:(Medium) rs760432755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489731,Human_RBP_ID_5141436,Human_RBP_ID_5316315,Human_RBP_ID_8082031,Human_RBP_ID_8725985,Human_RBP_ID_23273525,Human_RBP_ID_26768714,Human_RBP_ID_27655227 106660 RMVar_ID_106660 Human_SNP_ID_584552740 m1A Human chr15 - 79923164 79923164 79923164 CTTGCTAGACGACCTGGAGCGTCTGTCAGGCTAGGAGGAGGGGGAGGAGAGCTGGTGAGCGCCGG CTTGCTAGACGACCTGGAGCGTCTGTCAGGCTGGGAGGAGGGGGAGGAGAGCTGGTGAGCGCCGG T C ST20-MTHFS,AC015871.8,ST20 Ensembl:ENSG00000259332,Ensembl:ENSG00000288604,Ensembl:ENSG00000180953 Protein coding,Pseudogene,Protein coding intron,exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:79922969..79923218 26863196 MeRIP-seq:(Medium) rs1441646790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4756,Human_RBP_ID_260908,Human_RBP_ID_3488991,Human_RBP_ID_4342428,Human_RBP_ID_5087685,Human_RBP_ID_5316135,Human_RBP_ID_8182684,Human_RBP_ID_9324376,Human_RBP_ID_9418498,Human_RBP_ID_22048161,Human_RBP_ID_22711972,Human_RBP_ID_26778782 106661 RMVar_ID_106661 Human_SNP_ID_584588819 m1A Human chr15 - 80059743 80059743 80059743 GCCGCCGCCGGTAGCCGCCGGTGAATGGGTACAGGTAATGCCGCCGAACCCCTGCTTGCTCCGGC GCCGCCGCCGGTAGCCGCCGGTGAATGGGTACGGGTAATGCCGCCGAACCCCTGCTTGCTCCGGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:80059695..80059829 26863196 MeRIP-seq:(Medium) rs993659933 Functional Loss SNV dbSNP153 33..33 33 - - - 106662 RMVar_ID_106662 Human_SNP_ID_584588837 m1A Human chr15 - 80059784 80059784 80059784 TCCTCACCTGGCGGCGGGTCTCTCCGCCTGACACGCTGCGCGCCGCCGCCGGTAGCCGCCGGTGA TCCTCACCTGGCGGCGGGTCTCTCCGCCTGACGCGCTGCGCGCCGCCGCCGGTAGCCGCCGGTGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:80059676..80059862 26863196 MeRIP-seq:(Medium) rs1196999501 Functional Loss SNV dbSNP153 33..33 33 - - - 106663 RMVar_ID_106663 Human_SNP_ID_584613340 m1A Human chr15 - 80152837 80152837 80152837 AACCCCGAGCCCTGCCCCTCCCCCCTACCCTGACCCCCGCCAGCTCCAGGTCCTCCACAGTCTCG AACCCCGAGCCCTGCCCCTCCCCCCTACCCTGCCCCCCGCCAGCTCCAGGTCCTCCACAGTCTCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:80152787..80152968 26863196 MeRIP-seq:(Medium) rs1429108967 Functional Loss SNV dbSNP153 33..33 33 - - - 106664 RMVar_ID_106664 Human_SNP_ID_584721624 m1A Human chr15 + 80596442 80596442 80596442 GGGGGAGAAGCCCAGGACTGGGAGAATCGCACATGCCCCAGGGGTTTTCACCAAGGATTTTCAAG GGGGGAGAAGCCCAGGACTGGGAGAATCGCACGTGCCCCAGGGGTTTTCACCAAGGATTTTCAAG A G ARNT2 Ensembl:ENSG00000172379 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6495511 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14569,GWAS_ID_14570,GWAS_ID_14571 106665 RMVar_ID_106665 Human_SNP_ID_584746623 m1A Human chr15 - 80695274 80695274 80695274 CGCCCGGCGGCAGGAGGAGGCGGAGGCGGAGGAGGGCAGGAGGCGGGGCCGGCCCGGCGGGCGCG CGCCCGGCGGCAGGAGGAGGCGGAGGCGGAGGCGGGCAGGAGGCGGGGCCGGCCCGGCGGGCGCG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:80695180..80695529 26863410 MeRIP-seq:(Medium) rs1419414807 Functional Loss SNV dbSNP153 33..33 33 - - - 106666 RMVar_ID_106666 Human_SNP_ID_584750529 m1A Human chr15 + 80710127 80710127 80710127 ATGATTAGGGTATGCTTCATTCAGAGACTGACACATGGCCCCAAGCAGTGAGGGGTTAGCTATGT ATGATTAGGGTATGCTTCATTCAGAGACTGACGCATGGCCCCAAGCAGTGAGGGGTTAGCTATGT A G ABHD17C Ensembl:ENSG00000136379 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:80710121..80710268 26863196 MeRIP-seq:(Medium) rs1414763389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12612929 RMVar_hsa_circ_105367,RMVar_hsa_circ_174280 106667 RMVar_ID_106667 Human_SNP_ID_584750582 m1A Human chr15 - 80710352 80710352 80710352 CATTTCCTGCTGTCAAAGCCAAAGTCCCTGCAATGGTCTGCAAGGCCCTATGTGACTAATGCCCT CATTTCCTGCTGTCAAAGCCAAAGTCCCTGCAGTGGTCTGCAAGGCCCTATGTGACTAATGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:80710350..80710475 26863196 MeRIP-seq:(Medium) rs1003394314 Functional Loss SNV dbSNP153 33..33 33 - - - 106668 RMVar_ID_106668 Human_SNP_ID_584767351 m1A Human chr15 - 80779360 80779360 80779360 GGCTCTGCTTGAGCGCTAGCTCCCCGGCCCTCAGCCGAGAGGCCGCTTTTATAGCCACTTTTACT GGCTCTGCTTGAGCGCTAGCTCCCCGGCCCTCCGCCGAGAGGCCGCTTTTATAGCCACTTTTACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:80779329..80779394 26863196 MeRIP-seq:(Medium) rs1459609280 Functional Loss SNV dbSNP153 33..33 33 - - - 106669 RMVar_ID_106669 Human_SNP_ID_584815356 m1A Human chr15 - 80977083 80977083 80977083 GGAAGGCCAGCGGGGAGGCTGGGGCCCAGTGCAGGCCCAGGTTGGAGGAGCGTAGCACATGGAGT GGAAGGCCAGCGGGGAGGCTGGGGCCCAGTGCGGGCCCAGGTTGGAGGAGCGTAGCACATGGAGT T C MESD Ensembl:ENSG00000117899 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:80976933..80977300;chr15:80977034..80977292 26863196 MeRIP-seq:(Medium) rs1357337072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6471536 RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174306 106670 RMVar_ID_106670 Human_SNP_ID_584818844 m1A Human chr15 - 80989634 80989632 80989635 CGAGTCTACCCCACCTCCCCGGAAGAAGAAGAAGGATATTCGCGATTACAATGATGCAGACATGG CGAGTCTACCCCACCTCCCCGGAAGAAGAAG___GATATTCGCGATTACAATGATGCAGACATGG CCTT C MESD Ensembl:ENSG00000117899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:80989528..80989828 26863196 MeRIP-seq:(Medium) rs756097775 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1835652,Human_RBP_ID_4348204,Human_RBP_ID_9371199,Human_RBP_ID_18669862,Human_RBP_ID_22759451 Human_Splice_Rec_1634551,Human_Splice_Rec_1634559,Human_Splice_Rec_1634567,Human_Splice_Rec_1634581,Human_Splice_Rec_1634585 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 106671 RMVar_ID_106671 Human_SNP_ID_584818853 m1A Human chr15 - 80989659 80989659 80989659 CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTACCCCACCTCCCCGGAAGAAGAAGAAGGATATT CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTTCCCCACCTCCCCGGAAGAAGAAGAAGGATATT T A MESD Ensembl:ENSG00000117899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:80989578..80989828 26863196 MeRIP-seq:(Medium) rs536255319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41456,Human_RBP_ID_758531,Human_RBP_ID_1002346,Human_RBP_ID_4343361,Human_RBP_ID_9371199,Human_RBP_ID_22440172,Human_RBP_ID_22759451,Human_RBP_ID_25172128,Human_RBP_ID_26326354,Human_RBP_ID_27809801 Human_Splice_Rec_1634551,Human_Splice_Rec_1634559,Human_Splice_Rec_1634567,Human_Splice_Rec_1634581,Human_Splice_Rec_1634585 Human_miRNA_ID_1418276,Human_miRNA_ID_1702236,Human_miRNA_ID_2464241,Human_miRNA_ID_2561094 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 106672 RMVar_ID_106672 Human_SNP_ID_584818854 m1A Human chr15 - 80989659 80989659 80989659 CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTACCCCACCTCCCCGGAAGAAGAAGAAGGATATT CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTGCCCCACCTCCCCGGAAGAAGAAGAAGGATATT T C MESD Ensembl:ENSG00000117899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:80989578..80989828 26863196 MeRIP-seq:(Medium) rs536255319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41456,Human_RBP_ID_758531,Human_RBP_ID_1002346,Human_RBP_ID_4343361,Human_RBP_ID_9371199,Human_RBP_ID_22440172,Human_RBP_ID_22759451,Human_RBP_ID_25172128,Human_RBP_ID_26326354,Human_RBP_ID_27809801 Human_Splice_Rec_1634551,Human_Splice_Rec_1634559,Human_Splice_Rec_1634567,Human_Splice_Rec_1634581,Human_Splice_Rec_1634585 Human_miRNA_ID_1418276,Human_miRNA_ID_1702236,Human_miRNA_ID_2464241,Human_miRNA_ID_2561094 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 106673 RMVar_ID_106673 Human_SNP_ID_584818855 m1A Human chr15 - 80989659 80989659 80989659 CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTACCCCACCTCCCCGGAAGAAGAAGAAGGATATT CCGAAGGCTCGCCCGGGACGCCCGACGAGTCTCCCCCACCTCCCCGGAAGAAGAAGAAGGATATT T G MESD Ensembl:ENSG00000117899 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:80989578..80989828 26863196 MeRIP-seq:(Medium) rs536255319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_41456,Human_RBP_ID_758531,Human_RBP_ID_1002346,Human_RBP_ID_4343361,Human_RBP_ID_9371199,Human_RBP_ID_22440172,Human_RBP_ID_22759451,Human_RBP_ID_25172128,Human_RBP_ID_26326354,Human_RBP_ID_27809801 Human_Splice_Rec_1634551,Human_Splice_Rec_1634559,Human_Splice_Rec_1634567,Human_Splice_Rec_1634581,Human_Splice_Rec_1634585 Human_miRNA_ID_1418276,Human_miRNA_ID_1702236,Human_miRNA_ID_2464241,Human_miRNA_ID_2561094 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 106674 RMVar_ID_106674 Human_SNP_ID_584821870 m1A Human chr15 + 81000988 81000988 81000988 CCGAGGCGGCGGCGGCGGCGAGCCCGGGGGCGAGGCGCGGACGGGAACAGGAAAAGCCTCCGGCA CCGAGGCGGCGGCGGCGGCGAGCCCGGGGGCGCGGCGCGGACGGGAACAGGAAAAGCCTCCGGCA A C TLNRD1 Ensembl:ENSG00000140406 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:81000922..81002192;chr15:81000901..81002230;chr15:81000915..81002143 26863196 MeRIP-seq:(Medium) rs1349874378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4342890,Human_RBP_ID_5179575,Human_RBP_ID_5523475,Human_RBP_ID_8941212 106675 RMVar_ID_106675 Human_SNP_ID_584821892 m1A Human chr15 + 81001041 81001041 81001041 AAGCCTCCGGCAGCCCCTGCGGGCGGCGGCGCAGCCACGGCCGCGCTCCGAGGTGAAGCCGCGCG AAGCCTCCGGCAGCCCCTGCGGGCGGCGGCGCGGCCACGGCCGCGCTCCGAGGTGAAGCCGCGCG A G TLNRD1 Ensembl:ENSG00000140406 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:81000951..81001125 26863410 MeRIP-seq:(Medium) rs1342734319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232642,Human_RBP_ID_4342440,Human_RBP_ID_5523475,Human_RBP_ID_8941212 106676 RMVar_ID_106676 Human_SNP_ID_584822486 m1A Human chr15 + 81002531 81002531 81002531 GCAGTGCCGGGACACCATCATCGCGCGCACCAAGGGGCTCTCCATCCTCACCCACGACGTGCAGA GCAGTGCCGGGACACCATCATCGCGCGCACCACGGGGCTCTCCATCCTCACCCACGACGTGCAGA A C TLNRD1 Ensembl:ENSG00000140406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:81002491..81002642 26863196 MeRIP-seq:(Medium) rs201461230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27437617 Human_miRNA_ID_1024349,Human_miRNA_ID_1078363 106677 RMVar_ID_106677 Human_SNP_ID_584833885 m1A Human chr15 - 81050437 81050437 81050437 GCCTACCTGCCTCTCCAGCCTTATCTTGGGCTACACTCCACCCTCAGTTTCACTCCCTCACACTC GCCTACCTGCCTCTCCAGCCTTATCTTGGGCTGCACTCCACCCTCAGTTTCACTCCCTCACACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:81050387..81050505 26863196 MeRIP-seq:(Medium) rs1298568494 Functional Loss SNV dbSNP153 33..33 33 - - - 106678 RMVar_ID_106678 Human_SNP_ID_584849764 m1A Human chr15 - 81117778 81117778 81117778 TGAAGACGAAGATGTAGAAGGGGATGATGACAAAGATGAAGTCAGCGAGGAGGAAGAAGAATTTG TGAAGACGAAGATGTAGAAGGGGATGATGACAGAGATGAAGTCAGCGAGGAGGAAGAAGAATTTG T C ANP32BP3 Ensembl:ENSG00000259461 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:81117726..81117820 26863196 MeRIP-seq:(Medium) rs1211765265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18529315 106679 RMVar_ID_106679 Human_SNP_ID_584900366 m1A Human chr15 - 81324122 81324122 81324122 AGCGCCGCCGCTCATAACACCCGCGACCCCGCAGCTAAGCGCAGCTCCCGACGCAATGGACCCGG AGCGCCGCCGCTCATAACACCCGCGACCCCGCCGCTAAGCGCAGCTCCCGACGCAATGGACCCGG T G STARD5 Ensembl:ENSG00000172345 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:81323954..81324151 26863196 MeRIP-seq:(Medium) rs1189900791 Functional Loss SNV dbSNP153 33..33 33 - - - 106680 RMVar_ID_106680 Human_SNP_ID_585075214 m1A Human chr15 + 82043167 82043167 82043167 TGCGCACTAGCAGCGCCCGCTGCCTTTAAGAAAAGATGCGGATGGCCTGAGTGACCGCGGTGTGG TGCGCACTAGCAGCGCCCGCTGCCTTTAAGAAGAGATGCGGATGGCCTGAGTGACCGCGGTGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:82043116..82043216 32194978 MeRIP-seq:(Medium) rs1456762795 Functional Loss SNV dbSNP153 33..33 33 - - - 106681 RMVar_ID_106681 Human_SNP_ID_585075334 m1A Human chr15 - 82043413 82043413 82043413 CAACGGGCTGGGGGCACAGCTGCCTGGCTTGCAGCCGTCGGACACGTCGGGCTCCTCCTCTTCGT CAACGGGCTGGGGGCACAGCTGCCTGGCTTGCCGCCGTCGGACACGTCGGGCTCCTCCTCTTCGT T G MEX3B Ensembl:ENSG00000183496 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:82043364..82043513 32194978 MeRIP-seq:(Medium) rs1258465533 Functional Loss SNV dbSNP153 33..33 33 - - - 106682 RMVar_ID_106682 Human_SNP_ID_585076490 m1A Human chr15 - 82045645 82045637 82045646 AGCGCAACGGCAGCGGCGGCGGCGGCGGCGGCAGCAGCGGAGGGGGAGAGACCCTGGATGACCAA AGCGCAACGGCAGCGGCGGCGGCGGCGGCGG_________AGGGGGAGAGACCCTGGATGACCAA TCCGCTGCTG T MEX3B Ensembl:ENSG00000183496 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82045545..82046029 26863196 MeRIP-seq:(Medium) rs1567018066 Functional Loss DEL dbSNP153 32..40 33 - - - 106683 RMVar_ID_106683 Human_SNP_ID_585076494 m1A Human chr15 - 82045645 82045645 82045645 AGCGCAACGGCAGCGGCGGCGGCGGCGGCGGCAGCAGCGGAGGGGGAGAGACCCTGGATGACCAA AGCGCAACGGCAGCGGCGGCGGCGGCGGCGGCGGCAGCGGAGGGGGAGAGACCCTGGATGACCAA T C MEX3B Ensembl:ENSG00000183496 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82045545..82046029 26863196 MeRIP-seq:(Medium) rs1028115042 Functional Loss SNV dbSNP153 33..33 33 - - - 106684 RMVar_ID_106684 Human_SNP_ID_585076592 m1A Human chr15 - 82045841 82045841 82045841 CCGCACGGAGCGACCCACTCCTCCCAGCACCGAGGAAGAAGCAACGGAGCCCTCAGCAGGCGACC CCGCACGGAGCGACCCACTCCTCCCAGCACCGGGGAAGAAGCAACGGAGCCCTCAGCAGGCGACC T C MEX3B Ensembl:ENSG00000183496 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:82045793..82045943 32194978 MeRIP-seq:(Medium) rs1389498359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4336825 106685 RMVar_ID_106685 Human_SNP_ID_585129491 m1A Human chr15 + 82262854 82262854 82262854 ACGGCGGGCGCTGTGGGAGTGGAGAAGCTGCAAGTGCTGAGGCGCGGTGGAGGAAAGCATGGGAG ACGGCGGGCGCTGTGGGAGTGGAGAAGCTGCACGTGCTGAGGCGCGGTGGAGGAAAGCATGGGAG A C SAXO2 Ensembl:ENSG00000188659 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82262804..82262989 26863196 MeRIP-seq:(Medium) rs757055636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22934681 Human_Splice_Rec_1635381,Human_Splice_Rec_1635383,Human_Splice_Rec_1635389,Human_Splice_Rec_1635393,Human_Splice_Rec_1635399 106686 RMVar_ID_106686 Human_SNP_ID_585129492 m1A Human chr15 + 82262854 82262854 82262854 ACGGCGGGCGCTGTGGGAGTGGAGAAGCTGCAAGTGCTGAGGCGCGGTGGAGGAAAGCATGGGAG ACGGCGGGCGCTGTGGGAGTGGAGAAGCTGCAGGTGCTGAGGCGCGGTGGAGGAAAGCATGGGAG A G SAXO2 Ensembl:ENSG00000188659 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82262804..82262989 26863196 MeRIP-seq:(Medium) rs757055636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22934681 Human_Splice_Rec_1635381,Human_Splice_Rec_1635383,Human_Splice_Rec_1635389,Human_Splice_Rec_1635393,Human_Splice_Rec_1635399 106687 RMVar_ID_106687 Human_SNP_ID_585147835 m1A Human chr15 + 82344673 82344656 82344674 ACCCCAGCTCCAGCATCCTCTCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAGCCTCTCCAGCTCC ACCCCAGCTCCAGCAT__________________CCTCTCCAGCTCCCGCAGCCTCTCCAGCTCC TCCTCTCCAGCTCCCGCAG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344638..82344738;chr15:82344638..82344741 26863196 MeRIP-seq:(Medium) rs2005802 Functional Loss DEL dbSNP153 17..34 33 - - - 106688 RMVar_ID_106688 Human_SNP_ID_585147853 m1A Human chr15 + 82344673 82344673 82344673 ACCCCAGCTCCAGCATCCTCTCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAGCCTCTCCAGCTCC ACCCCAGCTCCAGCATCCTCTCCAGCTCCCGCGGCCTCTCCAGCTCCCGCAGCCTCTCCAGCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344638..82344738;chr15:82344638..82344741 26863196 MeRIP-seq:(Medium) rs764090500 Functional Loss SNV dbSNP153 33..33 33 - - - 106689 RMVar_ID_106689 Human_SNP_ID_585148137 m1A Human chr15 - 82344973 82344942 82345026 ATGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTAT ACGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTGT TAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACATAGCCTCTCCTCCTGTTCACGT CAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACAC GOLGA6L10 Ensembl:ENSG00000278662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344886..82345036;chr15:82344928..82345014 26863196 MeRIP-seq:(Medium) rs1567112041 Functional Loss MNV dbSNP153 1..64 33 - - - 106690 RMVar_ID_106690 Human_SNP_ID_585148138 m1A Human chr15 - 82344973 82344942 82345108 ATGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTAT ACGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTGT TAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACATAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCAC CAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCATGTAGCCTCTCCTCCTGTTCAT GOLGA6L10 Ensembl:ENSG00000278662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344886..82345036;chr15:82344928..82345014 26863196 MeRIP-seq:(Medium) rs1567112073 Functional Loss MNV dbSNP153 1..64 33 - - - 106691 RMVar_ID_106691 Human_SNP_ID_585148139 m1A Human chr15 - 82344973 82344942 82345109 ATGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTAT ACGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTGT TAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACATAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACA CAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCACGTAGCCTCTCCTCCTGTTCACACAGCCTCTCCTCCTGTTCATGTAGCCTCTCCTCCTGTTCATG GOLGA6L10 Ensembl:ENSG00000278662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344886..82345036;chr15:82344928..82345014 26863196 MeRIP-seq:(Medium) rs1567112074 Functional Loss MNV dbSNP153 1..64 33 - - - 106692 RMVar_ID_106692 Human_SNP_ID_585148169 m1A Human chr15 - 82344973 82344973 82344973 ATGTGAACAGGAGGAGAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTAT ATGTGAACAGGAGGAGAGGCTGTGTGAACAGGTGGAGAGGCTACGTGAACAGGAGGAGAGGCTAT T A GOLGA6L10 Ensembl:ENSG00000278662 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82344886..82345036;chr15:82344928..82345014 26863196 MeRIP-seq:(Medium) rs1370022859 Functional Loss SNV dbSNP153 33..33 33 - - - 106693 RMVar_ID_106693 Human_SNP_ID_585169764 m1A Human chr15 - 82434497 82434495 82434497 TCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAGAGTCTCCTGCTGCCACAGCCTCTCATCCTGTTG TCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAG__TCTCCTGCTGCCACAGCCTCTCATCCTGTTG ACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82434486..82434553;chr15:82434457..82434542 26863196 MeRIP-seq:(Medium) rs1188321430 Functional Loss DEL dbSNP153 33..34 33 - - - 106694 RMVar_ID_106694 Human_SNP_ID_585169767 m1A Human chr15 - 82434497 82434497 82434497 TCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAGAGTCTCCTGCTGCCACAGCCTCTCATCCTGTTG TCCAGCTCCCGCAGCCTCTCCAGCTCCCGCAGTGTCTCCTGCTGCCACAGCCTCTCATCCTGTTG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:82434486..82434553;chr15:82434457..82434542 26863196 MeRIP-seq:(Medium) rs1255413630 Functional Loss SNV dbSNP153 33..33 33 - - - 106695 RMVar_ID_106695 Human_SNP_ID_585193896 m1A Human chr15 + 82538985 82538985 82538985 CTCTGAATTCGCTTCATCAGATGCGTGACATAACTACAAAGCACACACAGCCAAAGAGAACAGTG CTCTGAATTCGCTTCATCAGATGCGTGACATAGCTACAAAGCACACACAGCCAAAGAGAACAGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr15:82538833..82539043;chr15:82538976..82539000;chr15:82538965..82539049;chr15:82538876..82539030 26863196,32194978 MeRIP-seq:(Medium) rs1289144824 Functional Loss SNV dbSNP153 33..33 33 - - - 106696 RMVar_ID_106696 Human_SNP_ID_585194194 m1A Human chr15 + 82540014 82540014 82540014 CTGCTATCTTGTTGCGGAGCTTTTTGCTGGGGATAATGGCGATCTCCTCGCACACGCGCTTGTTC CTGCTATCTTGTTGCGGAGCTTTTTGCTGGGGGTAATGGCGATCTCCTCGCACACGCGCTTGTTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:82539976..82540050 26863196 MeRIP-seq:(Medium) rs1031566468 Functional Loss SNV dbSNP153 33..33 33 - - - 106697 RMVar_ID_106697 Human_SNP_ID_585194254 m1A Human chr15 + 82540221 82540221 82540221 GCGGCGCCGAGCCCCGGCCGGTGTGGTTGGGGACCGCCGGCTGCGCTGAGCCGGAGAGGGCCCGG GCGGCGCCGAGCCCCGGCCGGTGTGGTTGGGGGCCGCCGGCTGCGCTGAGCCGGAGAGGGCCCGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:82540217..82540366 32194978 MeRIP-seq:(Medium) rs1290806033 Functional Loss SNV dbSNP153 33..33 33 - - - 106698 RMVar_ID_106698 Human_SNP_ID_585194292 m1A Human chr15 - 82540330 82540329 82540330 TCCTCAGCCCACAGAGAGGCCCTGGGCCGGGAAGGCGCAGAGCCCTGTCAGGCTGGAGCGCAACG TCCTCAGCCCACAGAGAGGCCCTGGGCCGGGA_GGCGCAGAGCCCTGTCAGGCTGGAGCGCAACG CT C AC245033.1,RPS17 Ensembl:ENSG00000260836,Ensembl:ENSG00000182774 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:82540318..82540475 26863196 MeRIP-seq:(Medium) rs1209736478 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5354646,Human_RBP_ID_19067528 RMVar_hsa_circ_106912,RMVar_hsa_circ_374772,RMVar_hsa_circ_174352,RMVar_hsa_circ_376408 106699 RMVar_ID_106699 Human_SNP_ID_585252333 m1A Human chr15 - 82750624 82750595 82750624 GACGCTGCTGTCACTGGCTCTGCTCGGTGGCCAGAGACAGTACTCACTCCATGCGGCCACCCCTC GACGCTGCTGTCACTGGCTCTGCTCGGTGGCC_____________________________CCTC GGGTGGCCGCATGGAGTGAGTACTGTCTCT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:82750576..82750775;chr15:82750576..82754631;chr15:82750576..82754679;chr15:82750575..82750775 26863196 MeRIP-seq:(Medium) rs1428757958 Functional Loss DEL dbSNP153 33..61 33 - - - 106700 RMVar_ID_106700 Human_SNP_ID_585267213 m1A Human chr15 - 82809852 82809852 82809852 CGCTGCTGCGCGGTACGGTCGTGACAAGTCACAGCGAACTTGCCCTCCGCGCCGTTCCAGGCCAC CGCTGCTGCGCGGTACGGTCGTGACAAGTCACGGCGAACTTGCCCTCCGCGCCGTTCCAGGCCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:82809631..82813141 26863196 MeRIP-seq:(Medium) rs1393543469 Functional Loss SNV dbSNP153 33..33 33 - - - 106701 RMVar_ID_106701 Human_SNP_ID_585267251 m1A Human chr15 + 82809923 82809911 82809923 GCGCGAGGGGGCCCGGTTGGGGCCCGAGCCCGAGCCCAAGCCTGAGGCCGCCGTCTCCCCGTCCA GCGCGAGGGGGCCCGGTTGGG____________GCCCAAGCCTGAGGCCGCCGTCTCCCCGTCCA GGCCCGAGCCCGA G WHAMM Ensembl:ENSG00000156232 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82809649..82810245 26863196 MeRIP-seq:(Medium) rs762622424 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_26778702 106702 RMVar_ID_106702 Human_SNP_ID_585267252 m1A Human chr15 + 82809923 82809911 82809923 GCGCGAGGGGGCCCGGTTGGGGCCCGAGCCCGAGCCCAAGCCTGAGGCCGCCGTCTCCCCGTCCA GCGCGAGGGGGCCCGGTTGGGGCCCGA______GCCCAAGCCTGAGGCCGCCGTCTCCCCGTCCA GGCCCGAGCCCGA GGCCCGA WHAMM Ensembl:ENSG00000156232 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82809649..82810245 26863196 MeRIP-seq:(Medium) rs762622424 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_26778702 106703 RMVar_ID_106703 Human_SNP_ID_585267362 m1A Human chr15 + 82810142 82810142 82810142 GCTGCTGTGGCCGACGCGCGCGGGTCCCGGCGAGGCGGCGCTGCAGGAGCTGTGCGGGCAGCTGG GCTGCTGTGGCCGACGCGCGCGGGTCCCGGCGGGGCGGCGCTGCAGGAGCTGTGCGGGCAGCTGG A G WHAMM Ensembl:ENSG00000156232 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:82810095..82810227 26863196 MeRIP-seq:(Medium) rs1343044967 Functional Loss SNV dbSNP153 33..33 33 - - - 106704 RMVar_ID_106704 Human_SNP_ID_585303135 m1A Human chr15 - 82952676 82952676 82952676 GGTGGCGGCAGTGGCAGCAGTGGCAGCCGCGCAGCCCCGCGGAATGGAGCGGCGCCGGGGCTGAG GGTGGCGGCAGTGGCAGCAGTGGCAGCCGCGCTGCCCCGCGGAATGGAGCGGCGCCGGGGCTGAG T A HOMER2 Ensembl:ENSG00000103942 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:82952541..82952685 26863196 MeRIP-seq:(Medium) rs1387009414 Functional Loss SNV dbSNP153 33..33 33 - - - 106705 RMVar_ID_106705 Human_SNP_ID_585310819 m1A Human chr15 - 82986371 82986371 82986371 CGCTCCCTCCTCCCGGGCGTCCGGGGCGACTCACCCGCCAAGGGCTATGTCAATCCAGCTCAGGC CGCTCCCTCCTCCCGGGCGTCCGGGGCGACTCCCCCGCCAAGGGCTATGTCAATCCAGCTCAGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:82986255..82987369 26863196 MeRIP-seq:(Medium) rs943715059 Functional Loss SNV dbSNP153 33..33 33 - - - 106706 RMVar_ID_106706 Human_SNP_ID_585316050 m1A Human chr15 - 83005409 83005409 83005409 GTGATGGCGCATGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GTGATGGCGCATGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1275959286 Functional Loss SNV dbSNP153 33..33 33 - - - 106707 RMVar_ID_106707 Human_SNP_ID_585317854 m1A Human chr15 - 83011579 83011579 83011579 GGGGATGCTGCGGCTCCGCAGCGGGCTGAGGCACCTTCGGGCAACACCCAATACTCGGGGCTCCG GGGGATGCTGCGGCTCCGCAGCGGGCTGAGGCGCCTTCGGGCAACACCCAATACTCGGGGCTCCG T C C15orf40 Ensembl:ENSG00000169609 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:83011512..83011581 26863196 MeRIP-seq:(Medium) rs553737044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125039,Human_RBP_ID_4342450,Human_RBP_ID_5418814,Human_RBP_ID_5494848,Human_RBP_ID_6473090,Human_RBP_ID_18418519,Human_RBP_ID_18670089 Human_Splice_Rec_1637305,Human_Splice_Rec_1637327,Human_Splice_Rec_1637337 106708 RMVar_ID_106708 Human_SNP_ID_585319342 m1A Human chr15 - 83017216 83017216 83017216 TTCAACATTGTGATAATCCTTCACAGCAAGAAACCGAATAAAATACTAACATTTCTAACAACTGC TTCAACATTGTGATAATCCTTCACAGCAAGAAGCCGAATAAAATACTAACATTTCTAACAACTGC T C BTBD1 Ensembl:ENSG00000064726 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:83017165..83017315 32194978 MeRIP-seq:(Medium) rs1018629673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465767,Human_RBP_ID_1835791,Human_RBP_ID_9057143,Human_RBP_ID_17251397,Human_RBP_ID_17366540,Human_RBP_ID_17484144,Human_RBP_ID_21924943,Human_RBP_ID_27655411 RMVar_hsa_circ_105101,RMVar_hsa_circ_174366 106709 RMVar_ID_106709 Human_SNP_ID_585332095 m1A Human chr15 - 83067023 83067023 83067023 TCTCTGGGGCCCCTGCTCCCCCTGCAGCGGGAACCTCTCTACAACTGGCAGGCGACCAAGGCGTC TCTCTGGGGCCCCTGCTCCCCCTGCAGCGGGAGCCTCTCTACAACTGGCAGGCGACCAAGGCGTC T C BTBD1 Ensembl:ENSG00000064726 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr15:83066926..83067180;chr15:83066942..83067226 26863410,26863196 MeRIP-seq:(Medium) rs774930502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465842,Human_RBP_ID_814520,Human_RBP_ID_4342907,Human_RBP_ID_5464330,Human_RBP_ID_17868168 106710 RMVar_ID_106710 Human_SNP_ID_585332151 m1A Human chr15 - 83067102 83067102 83067102 TGCCGCAGCTGGGGAGCAGGCGTCGGGGGCTGAGGCGGAGCCGGGCCCCGCGGGGCCGCCGCCGC TGCCGCAGCTGGGGAGCAGGCGTCGGGGGCTGTGGCGGAGCCGGGCCCCGCGGGGCCGCCGCCGC T A BTBD1 Ensembl:ENSG00000064726 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:83067006..83067106 26863410 MeRIP-seq:(Medium) rs759637648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232501,Human_RBP_ID_4342451,Human_RBP_ID_9324387 106711 RMVar_ID_106711 Human_SNP_ID_585332152 m1A Human chr15 - 83067102 83067102 83067102 TGCCGCAGCTGGGGAGCAGGCGTCGGGGGCTGAGGCGGAGCCGGGCCCCGCGGGGCCGCCGCCGC TGCCGCAGCTGGGGAGCAGGCGTCGGGGGCTGGGGCGGAGCCGGGCCCCGCGGGGCCGCCGCCGC T C BTBD1 Ensembl:ENSG00000064726 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:83067006..83067106 26863410 MeRIP-seq:(Medium) rs759637648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232501,Human_RBP_ID_4342451,Human_RBP_ID_9324387 106712 RMVar_ID_106712 Human_SNP_ID_585366304 m1A Human chr15 - 83207809 83207809 83207809 TGTTTGCGGTCGCTGCCCGAGAAGGAATTCGGAGCAGACGCGAGGCCCGGCGCTCGCGCCGCGCC TGTTTGCGGTCGCTGCCCGAGAAGGAATTCGGGGCAGACGCGAGGCCCGGCGCTCGCGCCGCGCC T C HDGFL3 Ensembl:ENSG00000166503 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:83207460..83207991 26863196 MeRIP-seq:(Medium) rs1043173499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3488999,Human_RBP_ID_8183427,Human_RBP_ID_9324605 106713 RMVar_ID_106713 Human_SNP_ID_585366305 m1A Human chr15 - 83207809 83207809 83207809 TGTTTGCGGTCGCTGCCCGAGAAGGAATTCGGAGCAGACGCGAGGCCCGGCGCTCGCGCCGCGCC TGTTTGCGGTCGCTGCCCGAGAAGGAATTCGGCGCAGACGCGAGGCCCGGCGCTCGCGCCGCGCC T G HDGFL3 Ensembl:ENSG00000166503 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:83207460..83207991 26863196 MeRIP-seq:(Medium) rs1043173499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3488999,Human_RBP_ID_8183427,Human_RBP_ID_9324605 106714 RMVar_ID_106714 Human_SNP_ID_585378720 m1A Human chr15 - 83257551 83257551 83257551 AACTGTGCACCTCCGGCAGCTCCACAAATGCAAAGTACCAGGCTGCAACACCATGTTTTCGTCTG AACTGTGCACCTCCGGCAGCTCCACAAATGCAGAGTACCAGGCTGCAACACCATGTTTTCGTCTG T C BNC1 Ensembl:ENSG00000169594 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:83257500..83257601 32194978 MeRIP-seq:(Medium) rs761648892 Functional Loss SNV dbSNP153 33..33 33 - - - 106715 RMVar_ID_106715 Human_SNP_ID_585380355 m1A Human chr15 - 83263938 83263938 83263938 GAACAGCCTGAACCTGGCCAGCTCTGAGAACTACAAGTGCCCAGGTTTCACAGTGACGTCCCCAG GAACAGCCTGAACCTGGCCAGCTCTGAGAACTCCAAGTGCCCAGGTTTCACAGTGACGTCCCCAG T G BNC1 Ensembl:ENSG00000169594 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:83263772..83264123 32194978 MeRIP-seq:(Medium) rs759486222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52225 106716 RMVar_ID_106716 Human_SNP_ID_585603472 m1A Human chr15 + 84239992 84239992 84239992 TGAACAGGAGGAGAGGCTACGTGAACAGGAGGAGAGGCTACGTGAACAGGAGGATAGGCTACATG TGAACAGGAGGAGAGGCTACGTGAACAGGAGGGGAGGCTACGTGAACAGGAGGATAGGCTACATG A G GOLGA6L4 Ensembl:ENSG00000184206 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:84239972..84240044;chr15:84239968..84240056 26863196 MeRIP-seq:(Medium) rs1317602383 Functional Loss SNV dbSNP153 33..33 33 - - - 106717 RMVar_ID_106717 Human_SNP_ID_585618024 m1A Human chr15 - 84389860 84389860 84389860 TGGGCCCCCTGTCCCCAGGACCCTGGCCAGCCAAGACTCACATCCCCAGGTGAGTGGTAACCACC TGGGCCCCCTGTCCCCAGGACCCTGGCCAGCCGAGACTCACATCCCCAGGTGAGTGGTAACCACC T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs191948173 Functional Loss SNV dbSNP153 33..33 33 - - - 106718 RMVar_ID_106718 Human_SNP_ID_585618025 m1A Human chr15 - 84389860 84389860 84389860 TGGGCCCCCTGTCCCCAGGACCCTGGCCAGCCAAGACTCACATCCCCAGGTGAGTGGTAACCACC TGGGCCCCCTGTCCCCAGGACCCTGGCCAGCCCAGACTCACATCCCCAGGTGAGTGGTAACCACC T G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs191948173 Functional Loss SNV dbSNP153 33..33 33 - - - 106719 RMVar_ID_106719 Human_SNP_ID_585621598 m1A Human chr15 - 84396334 84396334 84396334 TTAGACTTAGAAGTCTATGGCCAATGGCATCCAGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC TTAGACTTAGAAGTCTATGGCCAATGGCATCCTGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC T A - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1864257 Functional Loss SNV dbSNP153 33..33 33 - - - 106720 RMVar_ID_106720 Human_SNP_ID_585621599 m1A Human chr15 - 84396334 84396334 84396334 TTAGACTTAGAAGTCTATGGCCAATGGCATCCAGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC TTAGACTTAGAAGTCTATGGCCAATGGCATCCGGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1864257 Functional Loss SNV dbSNP153 33..33 33 - - - 106721 RMVar_ID_106721 Human_SNP_ID_585621600 m1A Human chr15 - 84396334 84396334 84396334 TTAGACTTAGAAGTCTATGGCCAATGGCATCCAGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC TTAGACTTAGAAGTCTATGGCCAATGGCATCCCGCTACCTGCCCTTCCTGCCTTCCCCAGGGTCC T G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1864257 Functional Loss SNV dbSNP153 33..33 33 - - - 106722 RMVar_ID_106722 Human_SNP_ID_585638806 m1A Human chr15 - 84512365 84512360 84512365 GAGGCTGTGTGAACAGGAGGAGAGGCTACGTGAACATGAGGAGAGGCTGTGTGAACAGGAGGAGA GAGGCTGTGTGAACAGGAGGAGAGGCTACGTG_____GAGGAGAGGCTGTGTGAACAGGAGGAGA CATGTT C GOLGA6L5P Ensembl:ENSG00000230373 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:84512314..84512398 26863196 MeRIP-seq:(Medium) rs1360091137 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3490674,Human_RBP_ID_5095771 106723 RMVar_ID_106723 Human_SNP_ID_585652366 m1A Human chr15 + 84570771 84570771 84570771 GCCGGTCGGGAGCCGCTGTCATGGCCGCGACCACCCGCGGGACCTCTCGGCGGCGCTCTCGCGGC GCCGGTCGGGAGCCGCTGTCATGGCCGCGACCCCCCGCGGGACCTCTCGGCGGCGCTCTCGCGGC A C LINC00933 Ensembl:ENSG00000259728 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84570727..84570792 26863196 MeRIP-seq:(Medium) rs927500365 Functional Loss SNV dbSNP153 33..33 33 - - - 106724 RMVar_ID_106724 Human_SNP_ID_585660256 m1A Human chr15 - 84604107 84604107 84604107 CTGGTCACCTCCTCCTGGGGGCCGCCCTTGCCAGCACTCTGGGGAAAGGGCTCAGACTCAGGGCC CTGGTCACCTCCTCCTGGGGGCCGCCCTTGCCGGCACTCTGGGGAAAGGGCTCAGACTCAGGGCC T C AC048382.5 Ensembl:ENSG00000275120 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:84604057..84604157 26863196 MeRIP-seq:(Medium) rs1042697262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358052 106725 RMVar_ID_106725 Human_SNP_ID_585663583 m1A Human chr15 - 84616363 84616363 84616363 GGGCTGGCTTCTTTGGTTCAGAGAGGCAAAGGAGGTGAGGCTGCAACTGGAATCACACAGGGCAG GGGCTGGCTTCTTTGGTTCAGAGAGGCAAAGGTGGTGAGGCTGCAACTGGAATCACACAGGGCAG T A AC048382.5 Ensembl:ENSG00000275120 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:84616354..84616437 26863196 MeRIP-seq:(Medium) rs1434669403 Functional Loss SNV dbSNP153 33..33 33 - - - 106726 RMVar_ID_106726 Human_SNP_ID_585668018 m1A Human chr15 + 84631532 84631532 84631532 CTGGGCTCGGGCTTCTTGCGTCCCCGCTAAGAACATGTCACGGGGCCGAATCGTCCGTATTCTCT CTGGGCTCGGGCTTCTTGCGTCCCCGCTAAGAGCATGTCACGGGGCCGAATCGTCCGTATTCTCT A G SCAND2P Ensembl:ENSG00000176700 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84631499..84631700 26863196 MeRIP-seq:(Medium) rs1022063928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1638293 106727 RMVar_ID_106727 Human_SNP_ID_585675637 m1A Human chr15 + 84658106 84658106 84658106 GCGGGGCGACGCCGGCAGCGAGCAGGGCGAAGAGCAGGAGGCTGCCGAACATCCGAGCGCCCCCC GCGGGGCGACGCCGGCAGCGAGCAGGGCGAAGGGCAGGAGGCTGCCGAACATCCGAGCGCCCCCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:84658059..84658185 26863196 MeRIP-seq:(Medium) rs1480735006 Functional Loss SNV dbSNP153 33..33 33 - - - 106728 RMVar_ID_106728 Human_SNP_ID_585675647 m1A Human chr15 - 84658125 84658125 84658125 CAGCCATGGCCCGGCGGGCGGGGGGCGCTCGGATGTTCGGCAGCCTCCTGCTCTTCGCCCTGCTC CAGCCATGGCCCGGCGGGCGGGGGGCGCTCGGGTGTTCGGCAGCCTCCTGCTCTTCGCCCTGCTC T C NMB Ensembl:ENSG00000197696 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:84658026..84658223 26863410 MeRIP-seq:(Medium) rs1419205041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466100,Human_RBP_ID_4343382,Human_RBP_ID_27437742 106729 RMVar_ID_106729 Human_SNP_ID_585678663 m1A Human chr15 + 84669952 84669952 84669952 ACGTGTGTTCTCCATTCCACCAATCACAGACCAGTATCTACTCCAAACATCCAGTAACGAAAACT ACGTGTGTTCTCCATTCCACCAATCACAGACCGGTATCTACTCCAAACATCCAGTAACGAAAACT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr15:84669852..84669996 26863196 MeRIP-seq:(Medium) rs985595650 Functional Loss SNV dbSNP153 33..33 33 - - - 106730 RMVar_ID_106730 Human_SNP_ID_585684228 m1A Human chr15 - 84691529 84691529 84691529 TGAAAGTCCGATTGTAGTGGTGCTCAGGTAACAGTTTTTCCTTTCAAGGCATGGAATTGCATGGC TGAAAGTCCGATTGTAGTGGTGCTCAGGTAACTGTTTTTCCTTTCAAGGCATGGAATTGCATGGC T A SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:84691526..84691650 32194978 MeRIP-seq:(Medium) rs780540085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888068,Human_RBP_ID_2457087,Human_RBP_ID_4348397,Human_RBP_ID_12620987 RMVar_hsa_circ_77057,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461,RMVar_hsa_circ_277529,RMVar_hsa_circ_174464,RMVar_hsa_circ_174463,RMVar_hsa_circ_301010,RMVar_hsa_circ_363353 106731 RMVar_ID_106731 Human_SNP_ID_585690288 m1A Human chr15 + 84716083 84716075 84716084 CGTCCAAAAAGTCTAGAGACAGCATGGCGGGGACGGCGAGCAGGACACCGGCAGGGGAAAGGGCG CGTCCAAAAAGTCTAGAGACAGCAT_________GGCGAGCAGGACACCGGCAGGGGAAAGGGCG TGGCGGGGAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:84715973..84716182 26863196 MeRIP-seq:(Medium) rs776084289 Functional Loss DEL dbSNP153 26..34 33 - - - 106732 RMVar_ID_106732 Human_SNP_ID_585690380 m1A Human chr15 - 84716281 84716281 84716281 CGGCGAGGCCAAGCCCTGAGACTGGACTAGCAAGGTCGTGAGTCTCTCTGTCAGCTCTCCGCAGC CGGCGAGGCCAAGCCCTGAGACTGGACTAGCAGGGTCGTGAGTCTCTCTGTCAGCTCTCCGCAGC T C SEC11A Ensembl:ENSG00000140612 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:84716233..84716354 32194978 MeRIP-seq:(Medium) rs1212987523 Functional Loss SNV dbSNP153 33..33 33 - - - 106733 RMVar_ID_106733 Human_SNP_ID_585698665 m1A Human chr15 - 84747698 84747698 84747698 GCTGGGAGGGTGACCGGCAGGACCTTCCAAGAACCCGGCGTACCTGGAAACTGGGTCCGCAGCAT GCTGGGAGGGTGACCGGCAGGACCTTCCAAGACCCCGGCGTACCTGGAAACTGGGTCCGCAGCAT T G lnc-SEC11A-2,lnc-SEC11A-2:2,lnc-SEC11A-2:3 RNACentral:URS00009B5F8F,RNACentral:URS00008C3622,RNACentral:URS00009B3477 lincRNA,lincRNA,lincRNA intron,exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84747649..84747964 26863196 MeRIP-seq:(Medium) rs780385040 Functional Loss SNV dbSNP153 33..33 33 - - - 106734 RMVar_ID_106734 Human_SNP_ID_585698976 m1A Human chr15 + 84748487 84748484 84748487 AGTCGCCTTCCGCCTGCCCCCCCCCCCCCCCAATCCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG AGTCGCCTTCCGCCTGCCCCCCCCCCCCCC___TCCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG CCAA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:84748376..84748625 26863410 MeRIP-seq:(Medium) rs1567054505 Functional Loss DEL dbSNP153 31..33 33 - - - 106735 RMVar_ID_106735 Human_SNP_ID_585698977 m1A Human chr15 + 84748487 84748485 84748488 AGTCGCCTTCCGCCTGCCCCCCCCCCCCCCCAATCCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG AGTCGCCTTCCGCCTGCCCCCCCCCCCCCCC___CCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG CAAT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:84748376..84748625 26863410 MeRIP-seq:(Medium) rs1567054512 Functional Loss DEL dbSNP153 32..34 33 - - - 106736 RMVar_ID_106736 Human_SNP_ID_585698979 m1A Human chr15 + 84748487 84748487 84748487 AGTCGCCTTCCGCCTGCCCCCCCCCCCCCCCAATCCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG AGTCGCCTTCCGCCTGCCCCCCCCCCCCCCCACTCCCCCGCCGCGGCAGCCCCAGCCAGGTCCCG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:84748376..84748625 26863410 MeRIP-seq:(Medium) rs1201131350 Functional Loss SNV dbSNP153 33..33 33 - - - 106737 RMVar_ID_106737 Human_SNP_ID_585699045 m1A Human chr15 + 84748663 84748663 84748663 GACTCTGGCCTGCAGTCGCCGCCGCCGCCGCCAGGTAAGCGCCCCCCGCGGGCCGGGCCGAGCGG GACTCTGGCCTGCAGTCGCCGCCGCCGCCGCCGGGTAAGCGCCCCCCGCGGGCCGGGCCGAGCGG A G ZNF592 Ensembl:ENSG00000166716 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84748613..84748699 26863196 MeRIP-seq:(Medium) rs1442169499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18418523 Human_Splice_Rec_1638607 106738 RMVar_ID_106738 Human_SNP_ID_585703652 m1A Human chr15 + 84766624 84766621 84766625 GCTGGAGAGTTGGGGGGCGGATAGAGAGACAGAGAGAGAGAGGACAGGGGAAGAGAAGAGAGGGA GCTGGAGAGTTGGGGGGCGGATAGAGAGAC____AGAGAGAGGACAGGGGAAGAGAAGAGAGGGA CAGAG C ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:84766612..84766741 26863196 MeRIP-seq:(Medium) rs1218857666 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5646446,Human_RBP_ID_25174425 RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106739 RMVar_ID_106739 Human_SNP_ID_585703653 m1A Human chr15 + 84766624 84766621 84766625 GCTGGAGAGTTGGGGGGCGGATAGAGAGACAGAGAGAGAGAGGACAGGGGAAGAGAAGAGAGGGA GCTGGAGAGTTGGGGGGCGGATAGAGAGACAG__AGAGAGAGGACAGGGGAAGAGAAGAGAGGGA CAGAG CAG ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:84766612..84766741 26863196 MeRIP-seq:(Medium) rs1218857666 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5646446,Human_RBP_ID_25174425 RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106740 RMVar_ID_106740 Human_SNP_ID_585703663 m1A Human chr15 + 84766658 84766658 84766658 AGAGAGAGGACAGGGGAAGAGAAGAGAGGGAGAGAAAGTGTACCGTGGAGGAAGGAATAGAGGGA AGAGAGAGGACAGGGGAAGAGAAGAGAGGGAGGGAAAGTGTACCGTGGAGGAAGGAATAGAGGGA A G ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:84766555..84766785 26863196 MeRIP-seq:(Medium) rs866139808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5646299,Human_RBP_ID_23671987 RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106741 RMVar_ID_106741 Human_SNP_ID_585704433 m1A Human chr15 + 84769422 84769422 84769422 TGGTTGGGTTGGGGATTGGTGTCTCATGTAGAACGGTCATGGAAGGCTCCTGACAAAGTGACATT TGGTTGGGTTGGGGATTGGTGTCTCATGTAGAGCGGTCATGGAAGGCTCCTGACAAAGTGACATT A G ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84769415..84769699 26863196 MeRIP-seq:(Medium) rs1426782840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12621983 RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106742 RMVar_ID_106742 Human_SNP_ID_585704462 m1A Human chr15 + 84769538 84769538 84769538 AGAATGTTTCAAGCAGAGGGAGTGGTGACTGCAGAGGCTCAGAATGGAGCATGACCAGCATGCCT AGAATGTTTCAAGCAGAGGGAGTGGTGACTGCGGAGGCTCAGAATGGAGCATGACCAGCATGCCT A G ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:84769530..84769657 26863196 MeRIP-seq:(Medium) rs1222468278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106743 RMVar_ID_106743 Human_SNP_ID_585706657 m1A Human chr15 + 84778304 84778304 84778304 GCCGAAAGAGGAGGTCCCTACCTGCCACGGATACCAGTCAGGTACACATGCAGAGGCTGGAGGAG GCCGAAAGAGGAGGTCCCTACCTGCCACGGATGCCAGTCAGGTACACATGCAGAGGCTGGAGGAG A G ZNF592 Ensembl:ENSG00000166716 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84778253..84778347 26863196 MeRIP-seq:(Medium) rs1281282194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885924,Human_RBP_ID_27809821 Human_Splice_Rec_1638611,Human_Splice_Rec_1638627 RMVar_hsa_circ_29930,RMVar_hsa_circ_339791,RMVar_hsa_circ_366494 106744 RMVar_ID_106744 Human_SNP_ID_585708314 m1A Human chr15 + 84784270 84784270 84784270 CAAGTCTTCAGTGCAAAGACGGAGCCAGCCACAGCTTACACAAATGTCGGTGCCCCTGGTCCACC CAAGTCTTCAGTGCAAAGACGGAGCCAGCCACCGCTTACACAAATGTCGGTGCCCCTGGTCCACC A C ZNF592 Ensembl:ENSG00000166716 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:84784219..84784332 26863196 MeRIP-seq:(Medium) rs1488351440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8802777,Human_RBP_ID_22194929,Human_RBP_ID_26327772 RMVar_hsa_circ_61544,RMVar_hsa_circ_29930,RMVar_hsa_circ_366494,RMVar_hsa_circ_120468,RMVar_hsa_circ_174466,RMVar_hsa_circ_6648 106745 RMVar_ID_106745 Human_SNP_ID_585712082 m1A Human chr15 - 84797970 84797970 84797970 GGTCTGCAGTGCTGCTGGCAGTCTTGAAGGCCATGGGGCAGAATGCACATTTGTGGAAAACCTGG GGTCTGCAGTGCTGCTGGCAGTCTTGAAGGCCCTGGGGCAGAATGCACATTTGTGGAAAACCTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84797920..84798001 26863196 MeRIP-seq:(Medium) rs781385610 Functional Loss SNV dbSNP153 33..33 33 - - - 106746 RMVar_ID_106746 Human_SNP_ID_585713392 m1A Human chr15 - 84802318 84802318 84802318 GCCTGTGGTTGACTGTGATCATTGTGGCCACCATCGTCCTCAGGGGCCGGGCCCAGCAATCTCCT GCCTGTGGTTGACTGTGATCATTGTGGCCACCGTCGTCCTCAGGGGCCGGGCCCAGCAATCTCCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:84802223..84802406 26863196 MeRIP-seq:(Medium) rs775528366 Functional Loss SNV dbSNP153 33..33 33 - - - 106747 RMVar_ID_106747 Human_SNP_ID_585761110 m1A Human chr15 + 84981735 84981725 84981735 CGGCGGCGGGAGCGGGGCCGGGCGCGGCCGGGAGCTCGCCTCCCCCGGGGGTCGTGCCGCAGCTC CGGCGGCGGGAGCGGGGCCGGGC__________GCTCGCCTCCCCCGGGGGTCGTGCCGCAGCTC CGCGGCCGGGA C PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84981546..84981937 26863196 MeRIP-seq:(Medium) rs1447731462 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_4343389,Human_RBP_ID_9324392,Human_RBP_ID_17652060,Human_RBP_ID_18458245,Human_RBP_ID_18481171,Human_RBP_ID_22047668 106748 RMVar_ID_106748 Human_SNP_ID_585763955 m1A Human chr15 - 84992547 84992547 84992547 CCTCACCCCACCTACTGCAATTTTTGCCTGAAACCTAATCTTCATGAAACATGTTTATCCTTTGA CCTCACCCCACCTACTGCAATTTTTGCCTGAACCCTAATCTTCATGAAACATGTTTATCCTTTGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84992541..84992755 26863196 MeRIP-seq:(Medium) rs1331055440 Functional Loss SNV dbSNP153 33..33 33 - - - 106749 RMVar_ID_106749 Human_SNP_ID_585772347 m1A Human chr15 - 85023507 85023507 85023507 TCCAATCCCACCTCCCCAGTTCTGTATAGACCACCATGGAGTCATAAACCACGTCTCCAAACAAA TCCAATCCCACCTCCCCAGTTCTGTATAGACCCCCATGGAGTCATAAACCACGTCTCCAAACAAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:85023500..85023783 26863196 MeRIP-seq:(Medium) rs533830574 Functional Loss SNV dbSNP153 33..33 33 - - - 106750 RMVar_ID_106750 Human_SNP_ID_585792914 m1A Human chr15 + 85101751 85101750 85101752 GGAATAATAAGGTGATGACAGTAGGAAGAGAGAAGAGAGACCAGATGTGATGATGGTGTGGGACT GGAATAATAAGGTGATGACAGTAGGAAGAGAG__GAGAGACCAGATGTGATGATGGTGTGGGACT GAA G PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:85101671..85101843 26863196 MeRIP-seq:(Medium) rs1443154193 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22496965 RMVar_hsa_circ_60082,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_370821,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174477,RMVar_hsa_circ_174478,RMVar_hsa_circ_308515,RMVar_hsa_circ_92480,RMVar_hsa_circ_174489,RMVar_hsa_circ_174490,RMVar_hsa_circ_174491,RMVar_hsa_circ_333903,RMVar_hsa_circ_89634,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_320896,RMVar_hsa_circ_55939,RMVar_hsa_circ_72645,RMVar_hsa_circ_4057,RMVar_hsa_circ_174497,RMVar_hsa_circ_16470,RMVar_hsa_circ_295651,RMVar_hsa_circ_307140,RMVar_hsa_circ_352659,RMVar_hsa_circ_315847,RMVar_hsa_circ_302365,RMVar_hsa_circ_74838,RMVar_hsa_circ_54869,RMVar_hsa_circ_174500,RMVar_hsa_circ_174501,RMVar_hsa_circ_316712,RMVar_hsa_circ_174502,RMVar_hsa_circ_94203 106751 RMVar_ID_106751 Human_SNP_ID_585793014 m1A Human chr15 + 85102172 85102172 85102172 GGAGGGGTGAGGTGGATTCCTAGAGACCACCCACCTCCAGAGAAGGAGGAAACAGAAGCAGGAAA GGAGGGGTGAGGTGGATTCCTAGAGACCACCCGCCTCCAGAGAAGGAGGAAACAGAAGCAGGAAA A G PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:85102004..85102407 26863196 MeRIP-seq:(Medium) rs1321249003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_370821,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174477,RMVar_hsa_circ_174478,RMVar_hsa_circ_308515,RMVar_hsa_circ_92480,RMVar_hsa_circ_174489,RMVar_hsa_circ_174490,RMVar_hsa_circ_174491,RMVar_hsa_circ_333903,RMVar_hsa_circ_89634,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_320896,RMVar_hsa_circ_55939,RMVar_hsa_circ_72645,RMVar_hsa_circ_4057,RMVar_hsa_circ_174497,RMVar_hsa_circ_16470,RMVar_hsa_circ_295651,RMVar_hsa_circ_307140,RMVar_hsa_circ_352659,RMVar_hsa_circ_315847,RMVar_hsa_circ_302365,RMVar_hsa_circ_74838,RMVar_hsa_circ_54869,RMVar_hsa_circ_174500,RMVar_hsa_circ_174501,RMVar_hsa_circ_316712,RMVar_hsa_circ_174502,RMVar_hsa_circ_94203 106752 RMVar_ID_106752 Human_SNP_ID_585796096 m1A Human chr15 + 85114875 85114875 85114875 GTAGGATAGTGTCCTGGAGGCGAGCAGATGAGAATAGCCACAGGACTGGAGAAAAGGGGCTGCTG GTAGGATAGTGTCCTGGAGGCGAGCAGATGAGTATAGCCACAGGACTGGAGAAAAGGGGCTGCTG A T PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:85114831..85115027 26863196 MeRIP-seq:(Medium) rs1189456346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5179582,Human_RBP_ID_12625022,Human_RBP_ID_25174881 RMVar_hsa_circ_60082,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_370821,RMVar_hsa_circ_322322,RMVar_hsa_circ_174477,RMVar_hsa_circ_174478,RMVar_hsa_circ_92480,RMVar_hsa_circ_174491,RMVar_hsa_circ_89634,RMVar_hsa_circ_174492,RMVar_hsa_circ_72645,RMVar_hsa_circ_16470,RMVar_hsa_circ_295651,RMVar_hsa_circ_307140,RMVar_hsa_circ_315847,RMVar_hsa_circ_302365,RMVar_hsa_circ_74838,RMVar_hsa_circ_54869,RMVar_hsa_circ_174500,RMVar_hsa_circ_174501,RMVar_hsa_circ_174502,RMVar_hsa_circ_94203,RMVar_hsa_circ_352503,RMVar_hsa_circ_71365,RMVar_hsa_circ_10901,RMVar_hsa_circ_271922,RMVar_hsa_circ_339585,RMVar_hsa_circ_71821,RMVar_hsa_circ_65151,RMVar_hsa_circ_174506,RMVar_hsa_circ_83380,RMVar_hsa_circ_273164,RMVar_hsa_circ_307095,RMVar_hsa_circ_174504,RMVar_hsa_circ_274206,RMVar_hsa_circ_271508,RMVar_hsa_circ_174507,RMVar_hsa_circ_174508,RMVar_hsa_circ_174505 106753 RMVar_ID_106753 Human_SNP_ID_585796137 m1A Human chr15 + 85115035 85115035 85115035 AGCTAATGTTTCCAGGAAAGCCTCGTGTCCTCAGAGTGAGGAGGGTTGCACGAAAATGGAGGAGA AGCTAATGTTTCCAGGAAAGCCTCGTGTCCTCCGAGTGAGGAGGGTTGCACGAAAATGGAGGAGA A C PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:85115013..85115078 26863196 MeRIP-seq:(Medium) rs1322475282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5179094 RMVar_hsa_circ_60082,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_370821,RMVar_hsa_circ_322322,RMVar_hsa_circ_174477,RMVar_hsa_circ_174478,RMVar_hsa_circ_92480,RMVar_hsa_circ_174491,RMVar_hsa_circ_89634,RMVar_hsa_circ_174492,RMVar_hsa_circ_72645,RMVar_hsa_circ_16470,RMVar_hsa_circ_295651,RMVar_hsa_circ_307140,RMVar_hsa_circ_315847,RMVar_hsa_circ_302365,RMVar_hsa_circ_74838,RMVar_hsa_circ_54869,RMVar_hsa_circ_174500,RMVar_hsa_circ_174501,RMVar_hsa_circ_174502,RMVar_hsa_circ_94203,RMVar_hsa_circ_352503,RMVar_hsa_circ_71365,RMVar_hsa_circ_10901,RMVar_hsa_circ_271922,RMVar_hsa_circ_339585,RMVar_hsa_circ_71821,RMVar_hsa_circ_65151,RMVar_hsa_circ_174506,RMVar_hsa_circ_83380,RMVar_hsa_circ_273164,RMVar_hsa_circ_307095,RMVar_hsa_circ_174504,RMVar_hsa_circ_274206,RMVar_hsa_circ_271508,RMVar_hsa_circ_174507,RMVar_hsa_circ_174508,RMVar_hsa_circ_174505 106754 RMVar_ID_106754 Human_SNP_ID_585801907 m1A Human chr15 + 85137912 85137912 85137912 AACCTCCGACCACCTCCTGAATAGTGGGAGACACCACCCAGAGCCCTGAAGCTTTGTTCCTTCGG AACCTCCGACCACCTCCTGAATAGTGGGAGACGCCACCCAGAGCCCTGAAGCTTTGTTCCTTCGG A G PDE8A Ensembl:ENSG00000073417 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:85137801..85138043 26863196 MeRIP-seq:(Medium) rs369249302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_935069,Human_miRNA_ID_954964,Human_miRNA_ID_2353960,Human_miRNA_ID_2424958,Human_miRNA_ID_2434621,Human_miRNA_ID_3069592 RMVar_hsa_circ_102922,RMVar_hsa_circ_174510 106755 RMVar_ID_106755 Human_SNP_ID_585864157 m1A Human chr15 - 85390449 85390449 85390449 TCACGCTCTTTCTCACCCATTCCAGCCACACCAGGCTCCCTGTTCATTCTCCCATCTCAGGTCCT TCACGCTCTTTCTCACCCATTCCAGCCACACCTGGCTCCCTGTTCATTCTCCCATCTCAGGTCCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:85390216..85390622 26863196 MeRIP-seq:(Medium) rs938063474 Functional Loss SNV dbSNP153 33..33 33 - - - 106756 RMVar_ID_106756 Human_SNP_ID_585864164 m1A Human chr15 - 85390467 85390467 85390467 CATACAAACCTTATCTCCTCACGCTCTTTCTCACCCATTCCAGCCACACCAGGCTCCCTGTTCAT CATACAAACCTTATCTCCTCACGCTCTTTCTCCCCCATTCCAGCCACACCAGGCTCCCTGTTCAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:85390230..85390721 26863196 MeRIP-seq:(Medium) rs1019935516 Functional Loss SNV dbSNP153 33..33 33 - - - 106757 RMVar_ID_106757 Human_SNP_ID_585979971 m1A Human chr15 - 85794888 85794888 85794888 CTAGTTTGTTGGCGGCGCCTAGGCTGTATCGCAGCGAGAGCGTTTTTGCCTGTGGAGAGCCGGCC CTAGTTTGTTGGCGGCGCCTAGGCTGTATCGCTGCGAGAGCGTTTTTGCCTGTGGAGAGCCGGCC T A KLHL25 Ensembl:ENSG00000183655 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:85794731..85794909 26863196 MeRIP-seq:(Medium) rs1042241711 Functional Loss SNV dbSNP153 33..33 33 - - - 106758 RMVar_ID_106758 Human_SNP_ID_585979972 m1A Human chr15 - 85794888 85794888 85794888 CTAGTTTGTTGGCGGCGCCTAGGCTGTATCGCAGCGAGAGCGTTTTTGCCTGTGGAGAGCCGGCC CTAGTTTGTTGGCGGCGCCTAGGCTGTATCGCGGCGAGAGCGTTTTTGCCTGTGGAGAGCCGGCC T C KLHL25 Ensembl:ENSG00000183655 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:85794731..85794909 26863196 MeRIP-seq:(Medium) rs1042241711 Functional Loss SNV dbSNP153 33..33 33 - - - 106759 RMVar_ID_106759 Human_SNP_ID_586750357 m1A Human chr15 - 88467752 88467752 88467752 ACCCGGCTGTCTGGGGCCAAGTCCAGGACCGCAGGAACCGCGACCCCGCGTTTCTCACAGCCTGC ACCCGGCTGTCTGGGGCCAAGTCCAGGACCGCCGGAACCGCGACCCCGCGTTTCTCACAGCCTGC T G AC013489.1 Ensembl:ENSG00000173867 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:88467701..88467809;chr15:88467701..88467829 26863196 MeRIP-seq:(Medium) rs777109331 Functional Loss SNV dbSNP153 33..33 33 - - - 106760 RMVar_ID_106760 Human_SNP_ID_586750490 m1A Human chr15 + 88467994 88467994 88467994 CCAAGACGCTGCGGCCAAGCAGAAAGTTGAACAGAACGCGGCTCCCAGCCACACCAAGTTCAGGT CCAAGACGCTGCGGCCAAGCAGAAAGTTGAACTGAACGCGGCTCCCAGCCACACCAAGTTCAGGT A T MRPS11 Ensembl:ENSG00000181991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:88467901..88468073 26863196 MeRIP-seq:(Medium) rs749231754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4338117,Human_RBP_ID_12627614,Human_RBP_ID_19067556 Human_Splice_Rec_1640652,Human_Splice_Rec_1640653,Human_Splice_Rec_1640662,Human_Splice_Rec_1640664,Human_Splice_Rec_1640665,Human_Splice_Rec_1640672,Human_Splice_Rec_1640682,Human_Splice_Rec_1640683,Human_Splice_Rec_1640686,Human_Splice_Rec_1640687,Human_Splice_Rec_1640696,Human_Splice_Rec_1640697,Human_Splice_Rec_1640703,Human_Splice_Rec_1640711 RMVar_hsa_circ_31117 106761 RMVar_ID_106761 Human_SNP_ID_586751701 m1A Human chr15 + 88472697 88472697 88472697 GGTGGGCAGGAAAGAAATTTGAGGAGATCCCAATTGCACACATTAAAGCATCCCACAACAAGTAA GGTGGGCAGGAAAGAAATTTGAGGAGATCCCAGTTGCACACATTAAAGCATCCCACAACAAGTAA A G MRPS11 Ensembl:ENSG00000181991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:88472598..88472761;chr15:88472632..88475037 26863196 MeRIP-seq:(Medium) rs1215019531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1510207,Human_RBP_ID_17251470 Human_Splice_Rec_1640654,Human_Splice_Rec_1640655,Human_Splice_Rec_1640674,Human_Splice_Rec_1640675,Human_Splice_Rec_1640688,Human_Splice_Rec_1640689,Human_Splice_Rec_1640704,Human_Splice_Rec_1640705,Human_Splice_Rec_1640713 RMVar_hsa_circ_31117,RMVar_hsa_circ_8942 106762 RMVar_ID_106762 Human_SNP_ID_586751702 m1A Human chr15 + 88472697 88472697 88472697 GGTGGGCAGGAAAGAAATTTGAGGAGATCCCAATTGCACACATTAAAGCATCCCACAACAAGTAA GGTGGGCAGGAAAGAAATTTGAGGAGATCCCATTTGCACACATTAAAGCATCCCACAACAAGTAA A T MRPS11 Ensembl:ENSG00000181991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr15:88472598..88472761;chr15:88472632..88475037 26863196 MeRIP-seq:(Medium) rs1215019531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1510207,Human_RBP_ID_17251470 Human_Splice_Rec_1640654,Human_Splice_Rec_1640655,Human_Splice_Rec_1640674,Human_Splice_Rec_1640675,Human_Splice_Rec_1640688,Human_Splice_Rec_1640689,Human_Splice_Rec_1640704,Human_Splice_Rec_1640705,Human_Splice_Rec_1640713 RMVar_hsa_circ_31117,RMVar_hsa_circ_8942 106763 RMVar_ID_106763 Human_SNP_ID_586761111 m1A Human chr15 - 88511263 88511263 88511263 TACGAATTTCACAAGGTAACTTTCAGCAGTCTAGAAGATGGCTTGGAGGGAATAGAGAGTAGAGG TACGAATTTCACAAGGTAACTTTCAGCAGTCTGGAAGATGGCTTGGAGGGAATAGAGAGTAGAGG T C DET1,AC013489.1 Ensembl:ENSG00000140543,Ensembl:ENSG00000173867 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:88511227..88511409 26863196 MeRIP-seq:(Medium) rs567205725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5568653 106764 RMVar_ID_106764 Human_SNP_ID_586763731 m1A Human chr15 + 88521156 88521156 88521156 GTACTCTGCCCCTCGCTCACTCCAGTCCAGCCACCCTGGCCTTCTTGTTGTCCCTCAAATGCATC GTACTCTGCCCCTCGCTCACTCCAGTCCAGCCTCCCTGGCCTTCTTGTTGTCCCTCAAATGCATC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:88521113..88521196 26863196 MeRIP-seq:(Medium) rs964921616 Functional Loss SNV dbSNP153 33..33 33 - - - 106765 RMVar_ID_106765 Human_SNP_ID_586794581 m1A Human chr15 - 88621378 88621378 88621378 CGCCCCGGTGCAGGGTCCTGGATCTCACCTGAAGCCCCGCGTGTCTCTTCCGGTCTGCACGTGGC CGCCCCGGTGCAGGGTCCTGGATCTCACCTGAGGCCCCGCGTGTCTCTTCCGGTCTGCACGTGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr15:88621365..88621440;chr15:88621363..88621447 26863196 MeRIP-seq:(Medium) rs937763377 Functional Loss SNV dbSNP153 33..33 33 - - - 106766 RMVar_ID_106766 Human_SNP_ID_586796046 m1A Human chr15 + 88626578 88626578 88626578 ATCGACTGTGAGATGGTGGGCACGGGACCCCGAGGGCGGGTAAGCGAGCTGGCCCGCTGTTCCAT ATCGACTGTGAGATGGTGGGCACGGGACCCCGCGGGCGGGTAAGCGAGCTGGCCCGCTGTTCCAT A C AEN Ensembl:ENSG00000181026 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:88626528..88626678 32194978 MeRIP-seq:(Medium) rs1330893926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232384,Human_RBP_ID_759295,Human_RBP_ID_815517,Human_RBP_ID_884869,Human_RBP_ID_6476932,Human_RBP_ID_17868661,Human_RBP_ID_22048280 RMVar_hsa_circ_90240,RMVar_hsa_circ_329795,RMVar_hsa_circ_174597 106767 RMVar_ID_106767 Human_SNP_ID_586797216 m1A Human chr15 + 88630227 88630227 88630227 CACAGACATGGAACAGTACATGGAGGACCAGTACTGGCCCGATGACCTGGCCCACGGCAGCAGAG CACAGACATGGAACAGTACATGGAGGACCAGTGCTGGCCCGATGACCTGGCCCACGGCAGCAGAG A G AEN Ensembl:ENSG00000181026 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:88630176..88630375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_232388,Human_RBP_ID_1510256,Human_RBP_ID_6476986,Human_RBP_ID_8425222,Human_RBP_ID_8802884,Human_RBP_ID_12628188,Human_RBP_ID_26936337 Human_miRNA_ID_1200828,Human_miRNA_ID_1351173,Human_miRNA_ID_1993776,Human_miRNA_ID_2662817,Human_miRNA_ID_2678901,Human_miRNA_ID_2681266,Human_miRNA_ID_3080945 RMVar_hsa_circ_90240,RMVar_hsa_circ_124659,RMVar_hsa_circ_121013,RMVar_hsa_circ_174597,RMVar_hsa_circ_174598,RMVar_hsa_circ_174599 106768 RMVar_ID_106768 Human_SNP_ID_586797359 m1A Human chr15 + 88630589 88630589 88630589 GGACCATCTTCTAGGGCCCAGCAGGAGTAGGGAATGTGCCAACAGACTGCCCAGGTTGCCGTGGC GGACCATCTTCTAGGGCCCAGCAGGAGTAGGGCATGTGCCAACAGACTGCCCAGGTTGCCGTGGC A C AEN Ensembl:ENSG00000181026 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:88630541..88630641 32194978 MeRIP-seq:(Medium) rs1280423395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815523,Human_RBP_ID_1002498,Human_RBP_ID_1510259,Human_RBP_ID_4338237,Human_RBP_ID_6477000,Human_RBP_ID_8802889,Human_RBP_ID_12628213,Human_RBP_ID_17868672,Human_RBP_ID_26436597,Human_RBP_ID_27655631 Human_miRNA_ID_392106,Human_miRNA_ID_398126,Human_miRNA_ID_404176,Human_miRNA_ID_410147,Human_miRNA_ID_1986924,Human_miRNA_ID_3123444 RMVar_hsa_circ_90240,RMVar_hsa_circ_124659,RMVar_hsa_circ_121013,RMVar_hsa_circ_174597,RMVar_hsa_circ_174598,RMVar_hsa_circ_174599 106769 RMVar_ID_106769 Human_SNP_ID_586797472 m1A Human chr15 + 88631038 88631038 88631038 GAAAGCCCCAGGCACAGCTCAGGGAGGAGGGAAGGCAGGTAAGCTTTGGACGAGAACTGGCATAT GAAAGCCCCAGGCACAGCTCAGGGAGGAGGGAGGGCAGGTAAGCTTTGGACGAGAACTGGCATAT A G AEN Ensembl:ENSG00000181026 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:88630988..88631089 32194978 MeRIP-seq:(Medium) rs536868202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1836322,Human_RBP_ID_6477022,Human_RBP_ID_12628240,Human_RBP_ID_17868680,Human_RBP_ID_22440475 RMVar_hsa_circ_90240,RMVar_hsa_circ_124659,RMVar_hsa_circ_121013,RMVar_hsa_circ_174597,RMVar_hsa_circ_174598,RMVar_hsa_circ_174599 106770 RMVar_ID_106770 Human_SNP_ID_586799956 m1A Human chr15 - 88639471 88639471 88639471 TCAGGCCGGATGAACTTGTCGTACAGCACAGCACCGTGGACGTTCACGAGGCTGCAACGAGCCAG TCAGGCCGGATGAACTTGTCGTACAGCACAGCTCCGTGGACGTTCACGAGGCTGCAACGAGCCAG T A lnc-DET1-4,lnc-DET1-4:2 RNACentral:URS00009B606E,RNACentral:URS00008B46D2 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:88639422..88639531 26863196 MeRIP-seq:(Medium) rs35008759 Functional Loss SNV dbSNP153 33..33 33 - - - 106771 RMVar_ID_106771 Human_SNP_ID_586799957 m1A Human chr15 - 88639471 88639471 88639471 TCAGGCCGGATGAACTTGTCGTACAGCACAGCACCGTGGACGTTCACGAGGCTGCAACGAGCCAG TCAGGCCGGATGAACTTGTCGTACAGCACAGCGCCGTGGACGTTCACGAGGCTGCAACGAGCCAG T C lnc-DET1-4,lnc-DET1-4:2 RNACentral:URS00009B606E,RNACentral:URS00008B46D2 lincRNA,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:88639422..88639531 26863196 MeRIP-seq:(Medium) rs35008759 Functional Loss SNV dbSNP153 33..33 33 - - - 106772 RMVar_ID_106772 Human_SNP_ID_586869218 m1A Human chr15 - 88887303 88887303 88887303 GGCCCCAGCCTGGCCCGGGTCACCCTGGCATGAGGAGATGGGCCTGTTGCTCCTGGTCCCGTTGC GGCCCCAGCCTGGCCCGGGTCACCCTGGCATGCGGAGATGGGCCTGTTGCTCCTGGTCCCGTTGC T G HAPLN3 Ensembl:ENSG00000140511 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:88887254..88892982 32194978 MeRIP-seq:(Medium) rs779109933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1176503,Human_RBP_ID_22650927 Human_Splice_Rec_1641060,Human_Splice_Rec_1641068,Human_Splice_Rec_1641080,Human_Splice_Rec_1641088,Human_Splice_Rec_1641096 106773 RMVar_ID_106773 Human_SNP_ID_586874199 m1A Human chr15 - 88903866 88903865 88903866 GGAAGGCCAGTGGAGCTGGAGCCAAGAGATGGAGGGGCAGCTTGGTGGGTGAAGAGCCCCAGGGA GGAAGGCCAGTGGAGCTGGAGCCAAGAGATGG_GGGGCAGCTTGGTGGGTGAAGAGCCCCAGGGA CT C MFGE8 Ensembl:ENSG00000140545 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:88903859..88903988 26863196 MeRIP-seq:(Medium) rs1383380296 Functional Loss DEL dbSNP153 33..33 33 - - - 106774 RMVar_ID_106774 Human_SNP_ID_586876027 m1A Human chr15 - 88909925 88909925 88909925 ATCATCTGCTCATCTTACCTGTCTCTGTCCCCAGATATCTGTTCCAAAAACCCCTGCCACAACGG ATCATCTGCTCATCTTACCTGTCTCTGTCCCCTGATATCTGTTCCAAAAACCCCTGCCACAACGG T A MFGE8 Ensembl:ENSG00000140545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:88909826..88909996 26863410 MeRIP-seq:(Medium) rs754854442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18670848,Human_RBP_ID_22473443,Human_RBP_ID_22650216 106775 RMVar_ID_106775 Human_SNP_ID_586922064 m1A Human chr15 + 89070179 89070177 89070180 ATCTGGAACATTACTAGTCTCCAGGCAGAAGAAAAAGAGACAATGGTGAGCCATGTGATTTTTCT ATCTGGAACATTACTAGTCTCCAGGCAGAAG___AAGAGACAATGGTGAGCCATGTGATTTTTCT GAAA G AC013565.1 Ensembl:ENSG00000260123 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs748708111 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1641216,Human_Splice_Rec_1641217,Human_Splice_Rec_1641222,Human_Splice_Rec_1641223 106776 RMVar_ID_106776 Human_SNP_ID_586926532 m1A Human chr15 + 89088515 89088514 89088515 TCCATGAGCGCCGCTGGCAGCCGGGGAGCTGCAGGAACCAGACTGGGGGCGAGCTGAGCACCTGT TCCATGAGCGCCGCTGGCAGCCGGGGAGCTGC_GGAACCAGACTGGGGGCGAGCTGAGCACCTGT CA C ABHD2 Ensembl:ENSG00000140526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89088465..89088603 26863196 MeRIP-seq:(Medium) rs1004594532 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_123175,Human_RBP_ID_759057,Human_RBP_ID_888144,Human_RBP_ID_4338418,Human_RBP_ID_22934687 Human_Splice_Rec_1641235,Human_Splice_Rec_1641243,Human_Splice_Rec_1641249,Human_Splice_Rec_1641259,Human_Splice_Rec_1641287,Human_Splice_Rec_1641307,Human_Splice_Rec_1641317 Human_miRNA_ID_2013395,Human_miRNA_ID_2469435,Human_miRNA_ID_2759787 RMVar_hsa_circ_119406,RMVar_hsa_circ_174605,RMVar_hsa_circ_89435,RMVar_hsa_circ_174604 106777 RMVar_ID_106777 Human_SNP_ID_586926533 m1A Human chr15 + 89088515 89088515 89088515 TCCATGAGCGCCGCTGGCAGCCGGGGAGCTGCAGGAACCAGACTGGGGGCGAGCTGAGCACCTGT TCCATGAGCGCCGCTGGCAGCCGGGGAGCTGCGGGAACCAGACTGGGGGCGAGCTGAGCACCTGT A G ABHD2 Ensembl:ENSG00000140526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89088465..89088603 26863196 MeRIP-seq:(Medium) rs1019600436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_123175,Human_RBP_ID_759057,Human_RBP_ID_888144,Human_RBP_ID_4338418,Human_RBP_ID_22934687 Human_Splice_Rec_1641235,Human_Splice_Rec_1641243,Human_Splice_Rec_1641249,Human_Splice_Rec_1641259,Human_Splice_Rec_1641287,Human_Splice_Rec_1641307,Human_Splice_Rec_1641317 Human_miRNA_ID_2013395,Human_miRNA_ID_2469435,Human_miRNA_ID_2759787 RMVar_hsa_circ_119406,RMVar_hsa_circ_174605,RMVar_hsa_circ_89435,RMVar_hsa_circ_174604 106778 RMVar_ID_106778 Human_SNP_ID_586966802 m1A Human chr15 - 89244046 89244046 89244046 AGCCCGAGCACCTCGCGAGCCGCTCTGCAGTCACCTCGGCCTCACCTCCGCCACAAACTTCCAAA AGCCCGAGCACCTCGCGAGCCGCTCTGCAGTCCCCTCGGCCTCACCTCCGCCACAAACTTCCAAA T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr15:89243976..89244128;chr15:89243976..89244123 26863410 MeRIP-seq:(Medium) rs1478677217 Functional Loss SNV dbSNP153 33..33 33 - - - 106779 RMVar_ID_106779 Human_SNP_ID_586967368 m1A Human chr15 + 89245582 89245582 89245582 GGAATTAGTAATAAAAGATTGGGGGGCAGTGGATGGAAGCAGGAATATTTATTTAAGTTCCAGAT GGAATTAGTAATAAAAGATTGGGGGGCAGTGGTTGGAAGCAGGAATATTTATTTAAGTTCCAGAT A T FANCI Ensembl:ENSG00000140525 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89245579..89258721 26863196 MeRIP-seq:(Medium) rs1459889921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6477482,Human_RBP_ID_20080313,Human_RBP_ID_23673300 RMVar_hsa_circ_106702,RMVar_hsa_circ_174629 106780 RMVar_ID_106780 Human_SNP_ID_586967383 m1A Human chr15 - 89245607 89245607 89245607 GCCACAGGCCCTTCCACATGTTTCCATCTGGAACTTAAATAAATATTCCTGCTTCCATCCACTGC GCCACAGGCCCTTCCACATGTTTCCATCTGGACCTTAAATAAATATTCCTGCTTCCATCCACTGC T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89245604..89245689 26863196 MeRIP-seq:(Medium) rs781400821 Functional Loss SNV dbSNP153 33..33 33 - - - 106781 RMVar_ID_106781 Human_SNP_ID_586967420 m1A Human chr15 - 89245758 89245757 89245758 TTCAGTGGCTTCCATTGCTTTATCAGTCCAAAACCCTTAAGTAAGGATAAAATAAGTCCTGCAAG TTCAGTGGCTTCCATTGCTTTATCAGTCCAAA_CCCTTAAGTAAGGATAAAATAAGTCCTGCAAG GT G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89245756..89245821 26863196 MeRIP-seq:(Medium) rs991280258 Functional Loss DEL dbSNP153 33..33 33 - - - 106782 RMVar_ID_106782 Human_SNP_ID_586972035 m1A Human chr15 + 89261624 89261624 89261624 ATTTTCCAGGACCATTATTGGTTGAATTAGCCAATGAGTTTATTAGTGCTGTCAGAGAAGGCAGC ATTTTCCAGGACCATTATTGGTTGAATTAGCCGATGAGTTTATTAGTGCTGTCAGAGAAGGCAGC A G FANCI Ensembl:ENSG00000140525 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:89261619..89261848 32194978 MeRIP-seq:(Medium) rs1555442689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42059,Human_RBP_ID_885174,Human_RBP_ID_1510364,Human_RBP_ID_1836414,Human_RBP_ID_4338610,Human_RBP_ID_12629715,Human_RBP_ID_18670906,Human_RBP_ID_23673341 Human_Splice_Rec_1641374,Human_Splice_Rec_1641452,Human_Splice_Rec_1641462,Human_Splice_Rec_1641536,Human_Splice_Rec_1641544,Human_Splice_Rec_1641558,Human_Splice_Rec_1641636,Human_Splice_Rec_1641652 RMVar_hsa_circ_16476,RMVar_hsa_circ_56441,RMVar_hsa_circ_106702,RMVar_hsa_circ_174629,RMVar_hsa_circ_351176,RMVar_hsa_circ_369456,RMVar_hsa_circ_349689,RMVar_hsa_circ_97405,RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_33118,RMVar_hsa_circ_17850,RMVar_hsa_circ_19539,RMVar_hsa_circ_17057,RMVar_hsa_circ_12328,RMVar_hsa_circ_68986,RMVar_hsa_circ_363315,RMVar_hsa_circ_174633,RMVar_hsa_circ_174635,RMVar_hsa_circ_11881,RMVar_hsa_circ_174634,RMVar_hsa_circ_366788,RMVar_hsa_circ_374412,RMVar_hsa_circ_322226,RMVar_hsa_circ_339324,RMVar_hsa_circ_303430,RMVar_hsa_circ_174636,RMVar_hsa_circ_10222,RMVar_hsa_circ_16660,RMVar_hsa_circ_174637,RMVar_hsa_circ_69940,RMVar_hsa_circ_331300,RMVar_hsa_circ_378431,RMVar_hsa_circ_40116,RMVar_hsa_circ_372515,RMVar_hsa_circ_321283,RMVar_hsa_circ_19540,RMVar_hsa_circ_174638 106783 RMVar_ID_106783 Human_SNP_ID_586980471 m1A Human chr15 - 89290276 89290276 89290276 CCATATATCCATAAAAATGTATTTTACCTGTGAGAGCAGAGTTTGCATGACTGAATTAGCCAGCT CCATATATCCATAAAAATGTATTTTACCTGTGGGAGCAGAGTTTGCATGACTGAATTAGCCAGCT T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:89285146..89290340 32194978 MeRIP-seq:(Medium) rs753059359 Functional Loss SNV dbSNP153 33..33 33 - - - 106784 RMVar_ID_106784 Human_SNP_ID_586981573 m1A Human chr15 - 89293994 89293994 89293994 TGTCTTTAAGCACTCTAGCAGAACCTTACCTGAAAAGAGCAGTGAGAAGACTGGACACAAATTTC TGTCTTTAAGCACTCTAGCAGAACCTTACCTGCAAAGAGCAGTGAGAAGACTGGACACAAATTTC T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:89293975..89295042 32194978 MeRIP-seq:(Medium) rs1427712731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12630610 106785 RMVar_ID_106785 Human_SNP_ID_586989300 m1A Human chr15 + 89316728 89316728 89316728 CCTGCACCACCCCGATGAAGCTCCACGGGAGCAAATACAGAGCCTCCAGGCAGTGCTATGGTCCA CCTGCACCACCCCGATGAAGCTCCACGGGAGCGAATACAGAGCCTCCAGGCAGTGCTATGGTCCA A G FANCI Ensembl:ENSG00000140525 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89316677..89316807 26863196 MeRIP-seq:(Medium) rs1481179865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1836545 RMVar_hsa_circ_118555,RMVar_hsa_circ_174642 106786 RMVar_ID_106786 Human_SNP_ID_586990112 m1A Human chr15 + 89318601 89318601 89318601 CCAGGGCAGCGCGGTAGCGGTCCTCCTCCCGCACCAGGTAGCGAACCTCGTCATGGATGCTGATG CCAGGGCAGCGCGGTAGCGGTCCTCCTCCCGCCCCAGGTAGCGAACCTCGTCATGGATGCTGATG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:89318576..89318600 32194978 MeRIP-seq:(Medium) rs1285172454 Functional Loss SNV dbSNP153 33..33 33 - - - 106787 RMVar_ID_106787 Human_SNP_ID_586990344 m1A Human chr15 - 89319055 89319054 89319055 GAAGTGGGAGGTGGTTGCTGAACGGGCATGGAAGGGGGGCACAGAGTCAGAAATGTTCAATAAGC GAAGTGGGAGGTGGTTGCTGAACGGGCATGGA_GGGGGGCACAGAGTCAGAAATGTTCAATAAGC CT C POLG Ensembl:ENSG00000140521 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89319004..89319120 26863196 MeRIP-seq:(Medium) rs1567185603 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_42047,Human_RBP_ID_466552,Human_RBP_ID_1836562,Human_RBP_ID_3945814,Human_RBP_ID_6478058,Human_RBP_ID_8425416,Human_RBP_ID_19067568,Human_RBP_ID_22650939,Human_RBP_ID_26327018 Human_Splice_Rec_1641832,Human_Splice_Rec_1641878,Human_Splice_Rec_1641888,Human_Splice_Rec_1641932,Human_Splice_Rec_1641974,Human_Splice_Rec_1642014,Human_Splice_Rec_1642058,Human_Splice_Rec_1642088,Human_Splice_Rec_1642128,Human_Splice_Rec_1642172,Human_Splice_Rec_1642200,Human_Splice_Rec_1642248,Human_Splice_Rec_1642262 Human_miRNA_ID_2454326,Human_miRNA_ID_2897008 Clinvar_Rec_683 RMVar_hsa_circ_375561,RMVar_hsa_circ_87036,RMVar_hsa_circ_174656,RMVar_hsa_circ_174657 106788 RMVar_ID_106788 Human_SNP_ID_586990445 m1A Human chr15 + 89319281 89319281 89319281 ACCTTGCGCAGATCCTGCAGGGAAATCCAGCCACCCTCAGTCCTGTCCACTGGGAGGTTCAACTC ACCTTGCGCAGATCCTGCAGGGAAATCCAGCCGCCCTCAGTCCTGTCCACTGGGAGGTTCAACTC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:89319121..89319300 26863196 MeRIP-seq:(Medium) rs1555452613 Functional Loss SNV dbSNP153 33..33 33 - - - 106789 RMVar_ID_106789 Human_SNP_ID_586991047 m1A Human chr15 + 89320918 89320918 89320918 ATGCGGCCGTAGTTGAAGATTTTGGCATGCTCACGGCTGATGCCCACAGTAGTGGCTGTCTTACT ATGCGGCCGTAGTTGAAGATTTTGGCATGCTCGCGGCTGATGCCCACAGTAGTGGCTGTCTTACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89320870..89320960 26863196 MeRIP-seq:(Medium) rs774005462 Functional Loss SNV dbSNP153 33..33 33 - - - 106790 RMVar_ID_106790 Human_SNP_ID_586992796 m1A Human chr15 - 89325159 89325079 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC_________________________________ AGTGAGAGAGTGAGTGAGTGAGAGAGTGAGAGAGAGTGAGTGAGTGAGTGAGAGAGTGAGTGAGAGAGTGAGTGAGTGAGT A POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs1567189163 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106791 RMVar_ID_106791 Human_SNP_ID_586992991 m1A Human chr15 - 89325159 89325143 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC________________TCTCACTCACTCTCTCA AGAGTGAGTGAGTGAGT A POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs368838895 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106792 RMVar_ID_106792 Human_SNP_ID_586992992 m1A Human chr15 - 89325159 89325143 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC____________ACTCTCTCACTCACTCTCTCA AGAGTGAGTGAGTGAGT AGAGT POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs368838895 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106793 RMVar_ID_106793 Human_SNP_ID_586992993 m1A Human chr15 - 89325159 89325143 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC________ACTCACTCTCTCACTCACTCTCTCA AGAGTGAGTGAGTGAGT AGAGTGAGT POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs368838895 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106794 RMVar_ID_106794 Human_SNP_ID_586992994 m1A Human chr15 - 89325159 89325143 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC____ACTCACTCACTCTCTCACTCACTCTCTCA AGAGTGAGTGAGTGAGT AGAGTGAGTGAGT POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs368838895 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106795 RMVar_ID_106795 Human_SNP_ID_586993031 m1A Human chr15 - 89325159 89325157 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTC__TCACTCACTCACTCTCTCACTCACTCTCTCA AGT A POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs1567189605 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106796 RMVar_ID_106796 Human_SNP_ID_586993032 m1A Human chr15 - 89325159 89325157 89325160 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACT___TCACTCACTCACTCTCTCACTCACTCTCTCA AGTG A POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs1567189606 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106797 RMVar_ID_106797 Human_SNP_ID_586993034 m1A Human chr15 - 89325159 89325159 89325159 ACTCACTCACTCTCTCACTCTCTCACTCACTCACTCACTCACTCACTCTCTCACTCACTCTCTCA ACTCACTCACTCTCTCACTCTCTCACTCACTCTCTCACTCACTCACTCTCTCACTCACTCTCTCA T A POLG Ensembl:ENSG00000140521 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89325044..89325273 26863196 MeRIP-seq:(Medium) rs62022592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197458,Human_RBP_ID_2458965,Human_RBP_ID_26756871 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106798 RMVar_ID_106798 Human_SNP_ID_586994161 m1A Human chr15 - 89327000 89327000 89327000 GAGTGGGACCTGCAAGAATTTAAGCAGAAGAAAGCTAAGAAGGTGAAGAAGGAACCAGCCACAGC GAGTGGGACCTGCAAGAATTTAAGCAGAAGAAGGCTAAGAAGGTGAAGAAGGAACCAGCCACAGC T C POLG Ensembl:ENSG00000140521 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89326949..89327304 26863196 MeRIP-seq:(Medium) rs1241518907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466561,Human_RBP_ID_1836576,Human_RBP_ID_2458974,Human_RBP_ID_3946674,Human_RBP_ID_26327021,Human_RBP_ID_27809853 Human_Splice_Rec_1641808,Human_Splice_Rec_1641809,Human_Splice_Rec_1641854,Human_Splice_Rec_1641855,Human_Splice_Rec_1641908,Human_Splice_Rec_1641909,Human_Splice_Rec_1641950,Human_Splice_Rec_1641951,Human_Splice_Rec_1641990,Human_Splice_Rec_1641991,Human_Splice_Rec_1642034,Human_Splice_Rec_1642035,Human_Splice_Rec_1642066,Human_Splice_Rec_1642067,Human_Splice_Rec_1642104,Human_Splice_Rec_1642105,Human_Splice_Rec_1642148,Human_Splice_Rec_1642149,Human_Splice_Rec_1642178,Human_Splice_Rec_1642179,Human_Splice_Rec_1642224,Human_Splice_Rec_1642225 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_46496,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660 106799 RMVar_ID_106799 Human_SNP_ID_586994245 m1A Human chr15 - 89327185 89327185 89327185 GTCGTTGATGGATCTGGCCAATGATGCCTGCCAGCTGCTCTCAGGAGAGAGGTAGCCAGGCCTTG GTCGTTGATGGATCTGGCCAATGATGCCTGCCCGCTGCTCTCAGGAGAGAGGTAGCCAGGCCTTG T G POLG Ensembl:ENSG00000140521 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89327095..89327186 26863196 MeRIP-seq:(Medium) rs886520102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_42050,Human_RBP_ID_232209,Human_RBP_ID_466562,Human_RBP_ID_885981,Human_RBP_ID_1836577,Human_RBP_ID_3946675,Human_RBP_ID_6478094,Human_RBP_ID_9371240,Human_RBP_ID_18671092,Human_RBP_ID_18981792,Human_RBP_ID_22934595,Human_RBP_ID_26327022,Human_RBP_ID_27809854 Human_Splice_Rec_1641807,Human_Splice_Rec_1641853,Human_Splice_Rec_1641907,Human_Splice_Rec_1641949,Human_Splice_Rec_1641989,Human_Splice_Rec_1642033,Human_Splice_Rec_1642065,Human_Splice_Rec_1642103,Human_Splice_Rec_1642147,Human_Splice_Rec_1642177,Human_Splice_Rec_1642223 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_120415,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_46496,RMVar_hsa_circ_174659,RMVar_hsa_circ_174660,RMVar_hsa_circ_174662,RMVar_hsa_circ_101751,RMVar_hsa_circ_371425,RMVar_hsa_circ_174661 106800 RMVar_ID_106800 Human_SNP_ID_586994296 m1A Human chr15 + 89327300 89327300 89327300 GTAACGCTCCCAGTTCTGGTTGACAGGCAGGTAGGAGACACCCATCTCCAGCATGCCGGCCAGAG GTAACGCTCCCAGTTCTGGTTGACAGGCAGGTGGGAGACACCCATCTCCAGCATGCCGGCCAGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:89327251..89327300 32194978 MeRIP-seq:(Medium) rs775538075 Functional Loss SNV dbSNP153 33..33 33 - - - 106801 RMVar_ID_106801 Human_SNP_ID_586996233 m1A Human chr15 + 89333375 89333368 89333375 GCTGGTCCAGGTTGTCCCCGTAGAGGGGCGGCAGGCGCAGCTCCACGTCGGGCAAGGGCACGGCT GCTGGTCCAGGTTGTCCCCGTAGAGG_______GGCGCAGCTCCACGTCGGGCAAGGGCACGGCT GGGCGGCA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:89333276..89333425 26863410 MeRIP-seq:(Medium) rs1064794735 Functional Loss DEL dbSNP153 27..33 33 - - - 106802 RMVar_ID_106802 Human_SNP_ID_586996371 m1A Human chr15 - 89333591 89333588 89333591 GCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAGCCTCAGCAGCCGCAAGTGCTATCCTCGGAGG GCAGCAGCAGCAGCAGCAGCAGCAGCAACAGC___CTCAGCAGCCGCAAGTGCTATCCTCGGAGG GGCT G POLG Ensembl:ENSG00000140521 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89333540..89333708 26863196 MeRIP-seq:(Medium) rs751908240 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4338920 Human_miRNA_ID_2715357,Human_miRNA_ID_3051335 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_80903,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174662,RMVar_hsa_circ_371425,RMVar_hsa_circ_174663,RMVar_hsa_circ_367580 106803 RMVar_ID_106803 Human_SNP_ID_586996382 m1A Human chr15 - 89333591 89333591 89333591 GCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAGCCTCAGCAGCCGCAAGTGCTATCCTCGGAGG GCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCCGCCTCAGCAGCCGCAAGTGCTATCCTCGGAGG T G POLG Ensembl:ENSG00000140521 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89333540..89333708 26863196 MeRIP-seq:(Medium) rs1223764065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4338920 Human_miRNA_ID_2715357,Human_miRNA_ID_3051335 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_80903,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174662,RMVar_hsa_circ_371425,RMVar_hsa_circ_174663,RMVar_hsa_circ_367580 106804 RMVar_ID_106804 Human_SNP_ID_586996613 m1A Human chr15 - 89333896 89333896 89333896 ATCTGTCTCCTTTAGGATTTGGGGTGGAAGGCAGGCATGGTCAAACCCATTTCACTGACAGGAGA ATCTGTCTCCTTTAGGATTTGGGGTGGAAGGCGGGCATGGTCAAACCCATTTCACTGACAGGAGA T C POLG Ensembl:ENSG00000140521 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89333846..89333936 26863196 MeRIP-seq:(Medium) rs944017900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5011,Human_RBP_ID_42055,Human_RBP_ID_759051,Human_RBP_ID_6478145,Human_RBP_ID_8941213,Human_RBP_ID_18671115,Human_RBP_ID_22048284,Human_RBP_ID_22540708,Human_RBP_ID_22650232,Human_RBP_ID_22737926,Human_RBP_ID_25177266,Human_RBP_ID_26327025 Human_Splice_Rec_1641796,Human_Splice_Rec_1641840,Human_Splice_Rec_1641896,Human_Splice_Rec_1642022,Human_Splice_Rec_1642136,Human_Splice_Rec_1642212,Human_Splice_Rec_1642332 RMVar_hsa_circ_375561,RMVar_hsa_circ_174656,RMVar_hsa_circ_16040,RMVar_hsa_circ_80903,RMVar_hsa_circ_83858,RMVar_hsa_circ_103224,RMVar_hsa_circ_174658,RMVar_hsa_circ_59181,RMVar_hsa_circ_174659,RMVar_hsa_circ_174662,RMVar_hsa_circ_371425,RMVar_hsa_circ_174663,RMVar_hsa_circ_367580 106805 RMVar_ID_106805 Human_SNP_ID_587062845 m1A Human chr15 + 89575816 89575816 89575816 CGAGCTGGGGTCCCGCTCGTGGGAGGACTTTGAGGAGGAGCTGGAGGCCAGGCTCGAGGATCGCG CGAGCTGGGGTCCCGCTCGTGGGAGGACTTTGCGGAGGAGCTGGAGGCCAGGCTCGAGGATCGCG A C AC013391.2,TICRR Ensembl:ENSG00000259713,Ensembl:ENSG00000140534 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89575766..89575995 26863196 MeRIP-seq:(Medium) rs761389345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232457,Human_RBP_ID_1130298,Human_RBP_ID_4348693,Human_RBP_ID_5096202,Human_RBP_ID_5523513,Human_RBP_ID_5570121,Human_RBP_ID_6478176,Human_RBP_ID_8803956,Human_RBP_ID_9284141,Human_RBP_ID_18189683,Human_RBP_ID_26326357,Human_RBP_ID_26768805 106806 RMVar_ID_106806 Human_SNP_ID_587062846 m1A Human chr15 + 89575816 89575816 89575816 CGAGCTGGGGTCCCGCTCGTGGGAGGACTTTGAGGAGGAGCTGGAGGCCAGGCTCGAGGATCGCG CGAGCTGGGGTCCCGCTCGTGGGAGGACTTTGGGGAGGAGCTGGAGGCCAGGCTCGAGGATCGCG A G AC013391.2,TICRR Ensembl:ENSG00000259713,Ensembl:ENSG00000140534 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89575766..89575995 26863196 MeRIP-seq:(Medium) rs761389345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232457,Human_RBP_ID_1130298,Human_RBP_ID_4348693,Human_RBP_ID_5096202,Human_RBP_ID_5523513,Human_RBP_ID_5570121,Human_RBP_ID_6478176,Human_RBP_ID_8803956,Human_RBP_ID_9284141,Human_RBP_ID_18189683,Human_RBP_ID_26326357,Human_RBP_ID_26768805 106807 RMVar_ID_106807 Human_SNP_ID_587062976 m1A Human chr15 - 89576056 89576056 89576056 GCAGCTCCCTCTGCGAGTGCGGACAGGGGGCCAGGAGGAAGACGGCGTTCACCAAGCCCCCGAGC GCAGCTCCCTCTGCGAGTGCGGACAGGGGGCCCGGAGGAAGACGGCGTTCACCAAGCCCCCGAGC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:89576011..89576142 26863196 MeRIP-seq:(Medium) rs1567037597 Functional Loss SNV dbSNP153 33..33 33 - - - 106808 RMVar_ID_106808 Human_SNP_ID_587066130 m1A Human chr15 - 89586677 89586677 89586677 CCCTGCCATCACTTCCTTCATGCCTTTGCTCAAATATCATTTTTTCAGCAAGGCCTTCCCTGACC CCCTGCCATCACTTCCTTCATGCCTTTGCTCACATATCATTTTTTCAGCAAGGCCTTCCCTGACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89586627..89586861 26863196 MeRIP-seq:(Medium) rs1269172005 Functional Loss SNV dbSNP153 33..33 33 - - - 106809 RMVar_ID_106809 Human_SNP_ID_587066306 m1A Human chr15 + 89587464 89587464 89587464 GGGTGGGCGTAGATGGGAAAGAGAAGGGGACTAAGGACTAACCCCTGCACCCTAATGTTAAGCAG GGGTGGGCGTAGATGGGAAAGAGAAGGGGACTGAGGACTAACCCCTGCACCCTAATGTTAAGCAG A G AC013391.2,TICRR Ensembl:ENSG00000259713,Ensembl:ENSG00000140534 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89587415..89587616 26863196 MeRIP-seq:(Medium) rs528429146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1087664,Human_RBP_ID_12631857,Human_RBP_ID_22933514 RMVar_hsa_circ_50825,RMVar_hsa_circ_4196,RMVar_hsa_circ_15398,RMVar_hsa_circ_43542,RMVar_hsa_circ_62496,RMVar_hsa_circ_104291,RMVar_hsa_circ_174686 106810 RMVar_ID_106810 Human_SNP_ID_587066596 m1A Human chr15 + 89588700 89588700 89588700 AACACGCTGGGGCACCAGAGGTGAGGAATTCAAGGGGACAAAGGCCAGAGTGTTGGTAGCATCAA AACACGCTGGGGCACCAGAGGTGAGGAATTCACGGGGACAAAGGCCAGAGTGTTGGTAGCATCAA A C AC013391.2,TICRR Ensembl:ENSG00000259713,Ensembl:ENSG00000140534 lincRNA,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:89588586..89588801 26863196 MeRIP-seq:(Medium) rs1179894683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247190,Human_RBP_ID_6478226,Human_RBP_ID_12631889 RMVar_hsa_circ_50825,RMVar_hsa_circ_4196,RMVar_hsa_circ_15398,RMVar_hsa_circ_43542,RMVar_hsa_circ_62496,RMVar_hsa_circ_104291,RMVar_hsa_circ_174686 106811 RMVar_ID_106811 Human_SNP_ID_587076283 m1A Human chr15 + 89624024 89624024 89624024 CCTCCAACTTCATCGACTGCCCAGCCCAGGAGAGAGTGTCTCACTCCCATCAGAGACCCTCTCAG CCTCCAACTTCATCGACTGCCCAGCCCAGGAGGGAGTGTCTCACTCCCATCAGAGACCCTCTCAG A G TICRR Ensembl:ENSG00000140534 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:89623976..89624075 26863196 MeRIP-seq:(Medium) rs1054307582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232226,Human_RBP_ID_5523523,Human_RBP_ID_9324403,Human_RBP_ID_22047699,Human_RBP_ID_22355488,Human_RBP_ID_26327033 RMVar_hsa_circ_104291,RMVar_hsa_circ_174686,RMVar_hsa_circ_85473,RMVar_hsa_circ_51405,RMVar_hsa_circ_50386,RMVar_hsa_circ_174692 106812 RMVar_ID_106812 Human_SNP_ID_587078071 m1A Human chr15 - 89628501 89628501 89628501 GCTTCCTGTGGGTGAGGCAGGCCTGCCCTGGAACTTTGGGCCTTTGTCCAAGCCCCGGCGGGAAC GCTTCCTGTGGGTGAGGCAGGCCTGCCCTGGACCTTTGGGCCTTTGTCCAAGCCCCGGCGGGAAC T G KIF7 Ensembl:ENSG00000166813 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:89628223..89631667 32194978 MeRIP-seq:(Medium) rs774442900 Functional Loss SNV dbSNP153 33..33 33 - - - 106813 RMVar_ID_106813 Human_SNP_ID_587079975 m1A Human chr15 - 89632891 89632891 89632891 AGCTGGGGGAGGAGCTCCACAAGCGGGAGGCCATCCTGGCCAAGAAGGAGGCCCTGATGCAGGAG AGCTGGGGGAGGAGCTCCACAAGCGGGAGGCCGTCCTGGCCAAGAAGGAGGCCCTGATGCAGGAG T C KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89632844..89632942 26863196 MeRIP-seq:(Medium) rs746496879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18982635 Human_Splice_Rec_1643075 106814 RMVar_ID_106814 Human_SNP_ID_587080205 m1A Human chr15 - 89633182 89633182 89633182 AAGAGATCGCGGCATTCCAGAGGAAGAGGCGCAGTGGCAGCAACGGCTCTGTGGTCAGCCTGGAA AAGAGATCGCGGCATTCCAGAGGAAGAGGCGCGGTGGCAGCAACGGCTCTGTGGTCAGCCTGGAA T C KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:89632973..89645106 32194978 MeRIP-seq:(Medium) rs1356594136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18982637 Human_Splice_Rec_1643072,Human_Splice_Rec_1643073 106815 RMVar_ID_106815 Human_SNP_ID_587080528 m1A Human chr15 - 89633859 89633859 89633859 GGTCCCAGGTGCTGAAGGAGAAGAAGCAGGCTACGGAGCGGCTGGTGTCACTGTCGGCCCAGAGT GGTCCCAGGTGCTGAAGGAGAAGAAGCAGGCTGCGGAGCGGCTGGTGTCACTGTCGGCCCAGAGT T C KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89633265..89642285 26863196 MeRIP-seq:(Medium) rs771441248 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5523528,Human_RBP_ID_18436984,Human_RBP_ID_24369232 Human_Splice_Rec_1643070 106816 RMVar_ID_106816 Human_SNP_ID_587084200 m1A Human chr15 - 89645415 89645415 89645415 AGGATCAGCAACTGCAGTCAGAGGGCGGGGGCACGCCCAGGGAGTCTGCCAGAGAGGAAGGGCCC AGGATCAGCAACTGCAGTCAGAGGGCGGGGGCGCGCCCAGGGAGTCTGCCAGAGAGGAAGGGCCC T C KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:89645374..89647015 32194978 MeRIP-seq:(Medium) rs1234199416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4339191 Human_Splice_Rec_1643064,Human_Splice_Rec_1643065 RMVar_hsa_circ_28624 106817 RMVar_ID_106817 Human_SNP_ID_587084401 m1A Human chr15 + 89645971 89645971 89645971 CCTCCTCTGAAGCAGCTGAAGAGCCACTTCCCAGCCTGTTCACCTCAGTCAGCAACTCAGCTCCA CCTCCTCTGAAGCAGCTGAAGAGCCACTTCCCGGCCTGTTCACCTCAGTCAGCAACTCAGCTCCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:89645892..89646019 26863196 MeRIP-seq:(Medium) rs1351864265 Functional Loss SNV dbSNP153 33..33 33 - - - 106818 RMVar_ID_106818 Human_SNP_ID_587085335 m1A Human chr15 - 89648598 89648598 89648598 CTGGCGGCCCGAGGCCGAGCGGCCACCCGAAGAGACGGCGAGCGGCGCGCGGGGTCCGCCACGGC CTGGCGGCCCGAGGCCGAGCGGCCACCCGAAGTGACGGCGAGCGGCGCGCGGGGTCCGCCACGGC T A KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:89648497..89648633 26863410 MeRIP-seq:(Medium) rs1255343241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28624 106819 RMVar_ID_106819 Human_SNP_ID_587085478 m1A Human chr15 + 89648967 89648967 89648967 CCGGCCCCCAGGCCACATAGGAGCCAGGGGGCAGCTCACCGGGTGATCTTGGAGTCGCGGTAGGG CCGGCCCCCAGGCCACATAGGAGCCAGGGGGCGGCTCACCGGGTGATCTTGGAGTCGCGGTAGGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89648963..89649075 26863196 MeRIP-seq:(Medium) rs1234898726 Functional Loss SNV dbSNP153 33..33 33 - - - 106820 RMVar_ID_106820 Human_SNP_ID_587086557 m1A Human chr15 + 89652694 89652694 89652694 ACAGTGGCATTGAAGCCCTCGAAGAAGGCCTCAAGGAGGGGCTGAACGCAGGCCTGGTACACGGC ACAGTGGCATTGAAGCCCTCGAAGAAGGCCTCGAGGAGGGGCTGAACGCAGGCCTGGTACACGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89652643..89652936 26863196 MeRIP-seq:(Medium) rs1046388085 Functional Loss SNV dbSNP153 33..33 33 - - - 106821 RMVar_ID_106821 Human_SNP_ID_587086587 m1A Human chr15 - 89652740 89652740 89652740 ACACTTTGGCTTCCACGTGGTGCTGGCCGAGGATGCGGGGCAGGAGGCCGTGTACCAGGCCTGCG ACACTTTGGCTTCCACGTGGTGCTGGCCGAGGGTGCGGGGCAGGAGGCCGTGTACCAGGCCTGCG T C KIF7 Ensembl:ENSG00000166813 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89652692..89652893 26863196 MeRIP-seq:(Medium) rs1026564700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2151843,Human_miRNA_ID_2420310 RMVar_hsa_circ_104402,RMVar_hsa_circ_174695 106822 RMVar_ID_106822 Human_SNP_ID_587096875 m1A Human chr15 - 89690668 89690668 89690668 GGATCCGACGGGCCCCAGAGGACCCACGCCTGAGCCCCGTGCGACTCGTGGCCTTTGGGCTAGAA GGATCCGACGGGCCCCAGAGGACCCACGCCTGTGCCCCGTGCGACTCGTGGCCTTTGGGCTAGAA T A PEX11A Ensembl:ENSG00000166821 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89690617..89690702 26863196 MeRIP-seq:(Medium) rs1431291923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1643131,Human_Splice_Rec_1643135,Human_Splice_Rec_1643139,Human_Splice_Rec_1643143,Human_Splice_Rec_1643147 106823 RMVar_ID_106823 Human_SNP_ID_587096879 m1A Human chr15 - 89690684 89690684 89690684 ACTGACCGTTCCCTGGGGATCCGACGGGCCCCAGAGGACCCACGCCTGAGCCCCGTGCGACTCGT ACTGACCGTTCCCTGGGGATCCGACGGGCCCCGGAGGACCCACGCCTGAGCCCCGTGCGACTCGT T C PEX11A Ensembl:ENSG00000166821 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89690638..89690721 26863196 MeRIP-seq:(Medium) rs1331987415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4348733 106824 RMVar_ID_106824 Human_SNP_ID_587110665 m1A Human chr15 + 89746523 89746499 89746523 ACAGCCCCGCCTCCACACACACACACAGCCCAACCTCCACACACGCACACACAGCCCAACCTCCA ACAGCCCCG________________________CCTCCACACACGCACACACAGCCCAACCTCCA GCCTCCACACACACACACAGCCCAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89746010..89746748 26863196 MeRIP-seq:(Medium) rs367927591 Functional Loss DEL dbSNP153 10..33 33 - - - 106825 RMVar_ID_106825 Human_SNP_ID_587110667 m1A Human chr15 - 89746502 89746502 89746502 GTGTGTGGAGGTTGGGCTGTGTGTGTGTGTGGAGGCGGGGCTGTGTGTGTAGAGGCAGGGCTGTG GTGTGTGGAGGTTGGGCTGTGTGTGTGTGTGGGGGCGGGGCTGTGTGTGTAGAGGCAGGGCTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89746038..89746703 26863196 MeRIP-seq:(Medium) rs1434847162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23673785 106826 RMVar_ID_106826 Human_SNP_ID_587110675 m1A Human chr15 + 89746523 89746511 89746524 ACAGCCCCGCCTCCACACACACACACAGCCCAACCTCCACACACGCACACACAGCCCAACCTCCA ACAGCCCCGCCTCCACACACA_____________CTCCACACACGCACACACAGCCCAACCTCCA ACACACAGCCCAAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89746010..89746748 26863196 MeRIP-seq:(Medium) rs1264851993 Functional Loss DEL dbSNP153 22..34 33 - - - 106827 RMVar_ID_106827 Human_SNP_ID_587110681 m1A Human chr15 + 89746523 89746523 89746523 ACAGCCCCGCCTCCACACACACACACAGCCCAACCTCCACACACGCACACACAGCCCAACCTCCA ACAGCCCCGCCTCCACACACACACACAGCCCAGCCTCCACACACGCACACACAGCCCAACCTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89746010..89746748 26863196 MeRIP-seq:(Medium) rs1471602895 Functional Loss SNV dbSNP153 33..33 33 - - - 106828 RMVar_ID_106828 Human_SNP_ID_587110829 m1A Human chr15 + 89746841 89746822 89746842 CCCCACCTCCACAAACACACAGCCCCGCCTCCACACACACAGCCCTGCCGCCACACACACACACA CCCCACCTCCACAA____________________ACACACAGCCCTGCCGCCACACACACACACA AACACACAGCCCCGCCTCCAC A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89746759..89746915 26863196 MeRIP-seq:(Medium) rs1309351505 Functional Loss DEL dbSNP153 15..34 33 - - - 106829 RMVar_ID_106829 Human_SNP_ID_587110881 m1A Human chr15 + 89746917 89746915 89746917 GCTGCCCCAGCCACACACACAGCCCCGCCTCCACACACAGCCCCACCTCCACACACACACACACA GCTGCCCCAGCCACACACACAGCCCCGCCTC__CACACAGCCCCACCTCCACACACACACACACA CCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89746866..89746975 26863196 MeRIP-seq:(Medium) rs559849312 Functional Loss DEL dbSNP153 32..33 33 - - - 106830 RMVar_ID_106830 Human_SNP_ID_587112210 m1A Human chr15 + 89750655 89750655 89750655 GGATCCCCAGGACGCCCCGGCGCGGACGGCGGATACCAGGCCCAGCCCGCGCCCCTGCCCCTGCC GGATCCCCAGGACGCCCCGGCGCGGACGGCGGCTACCAGGCCCAGCCCGCGCCCCTGCCCCTGCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:89750569..89750718 26863410 MeRIP-seq:(Medium) rs1358919134 Functional Loss SNV dbSNP153 33..33 33 - - - 106831 RMVar_ID_106831 Human_SNP_ID_587112211 m1A Human chr15 - 89750656 89750656 89750656 GGGCAGGGGCAGGGGCGCGGGCTGGGCCTGGTATCCGCCGTCCGCGCCGGGGCGTCCTGGGGATC GGGCAGGGGCAGGGGCGCGGGCTGGGCCTGGTGTCCGCCGTCCGCGCCGGGGCGTCCTGGGGATC T C MESP1 Ensembl:ENSG00000166823 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr15:89750569..89750669 26863410 MeRIP-seq:(Medium) rs756287418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5494914 106832 RMVar_ID_106832 Human_SNP_ID_587135508 m1A Human chr15 - 89830641 89830641 89830641 TTCAGTGCTGCATCCCAGCTGCTGGGCACGGTACCTGGTCCATGGCGTTCAATAAATAACTGTTG TTCAGTGCTGCATCCCAGCTGCTGGGCACGGTGCCTGGTCCATGGCGTTCAATAAATAACTGTTG T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466626 GWAS_ID_14572,GWAS_ID_14573,GWAS_ID_14574,GWAS_ID_14575,GWAS_ID_14576,GWAS_ID_14577,GWAS_ID_14578,GWAS_ID_14579,GWAS_ID_14580,GWAS_ID_14581,GWAS_ID_14582,GWAS_ID_14583,GWAS_ID_14584,GWAS_ID_14585,GWAS_ID_14586,GWAS_ID_14587,GWAS_ID_14588,GWAS_ID_14589,GWAS_ID_14590,GWAS_ID_14591,GWAS_ID_14592,GWAS_ID_14593,GWAS_ID_14594,GWAS_ID_14595,GWAS_ID_14596,GWAS_ID_14597,GWAS_ID_14598,GWAS_ID_14599,GWAS_ID_14600,GWAS_ID_14601,GWAS_ID_14602,GWAS_ID_14603,GWAS_ID_14604,GWAS_ID_14605,GWAS_ID_14606,GWAS_ID_14607,GWAS_ID_14608,GWAS_ID_14609,GWAS_ID_14610,GWAS_ID_14611,GWAS_ID_14612,GWAS_ID_14613,GWAS_ID_14614,GWAS_ID_14615,GWAS_ID_14616,GWAS_ID_14617,GWAS_ID_14618,GWAS_ID_14619,GWAS_ID_14620,GWAS_ID_14621,GWAS_ID_14622,GWAS_ID_14623,GWAS_ID_14624,GWAS_ID_14625,GWAS_ID_14626,GWAS_ID_14627,GWAS_ID_14628,GWAS_ID_14629,GWAS_ID_14630,GWAS_ID_14631,GWAS_ID_14632,GWAS_ID_14633,GWAS_ID_14634,GWAS_ID_14635,GWAS_ID_14636,GWAS_ID_14637,GWAS_ID_14638,GWAS_ID_14639,GWAS_ID_14640,GWAS_ID_14641,GWAS_ID_14642,GWAS_ID_14643,GWAS_ID_14644,GWAS_ID_14645,GWAS_ID_14646,GWAS_ID_14647,GWAS_ID_14648,GWAS_ID_14649,GWAS_ID_14650,GWAS_ID_14651,GWAS_ID_14652,GWAS_ID_14653,GWAS_ID_14654,GWAS_ID_14655,GWAS_ID_14656,GWAS_ID_14657,GWAS_ID_14658,GWAS_ID_14659,GWAS_ID_14660 RMVar_hsa_circ_84501,RMVar_hsa_circ_100602,RMVar_hsa_circ_105513,RMVar_hsa_circ_85390,RMVar_hsa_circ_174705,RMVar_hsa_circ_174707,RMVar_hsa_circ_174708,RMVar_hsa_circ_174706 106833 RMVar_ID_106833 Human_SNP_ID_587135906 m1A Human chr15 - 89832262 89832262 89832262 GTTTTATTTTTTTAGTAGAATAAGGTCTCACTATGTTGCACAGGCTGGTCTCTAACTCCTTACCT GTTTTATTTTTTTAGTAGAATAAGGTCTCACTGTGTTGCACAGGCTGGTCTCTAACTCCTTACCT T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1356486587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84501,RMVar_hsa_circ_100602,RMVar_hsa_circ_105513,RMVar_hsa_circ_85390,RMVar_hsa_circ_174705,RMVar_hsa_circ_174707,RMVar_hsa_circ_174708,RMVar_hsa_circ_174706 106834 RMVar_ID_106834 Human_SNP_ID_587143518 m1A Human chr15 - 89859267 89859263 89859268 AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAAGAAAAAAAGGAAGGAAGGAGGGAAAAAGAAAGAA AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAA_____AAAGGAAGGAAGGAGGGAAAAAGAAAGAA TTTTTC T AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89859141..89859372 26863196 MeRIP-seq:(Medium) rs905112405 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_25177874 RMVar_hsa_circ_84501,RMVar_hsa_circ_100602,RMVar_hsa_circ_174707,RMVar_hsa_circ_174708,RMVar_hsa_circ_174709,RMVar_hsa_circ_359072 106835 RMVar_ID_106835 Human_SNP_ID_587143520 m1A Human chr15 - 89859267 89859265 89859268 AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAAGAAAAAAAGGAAGGAAGGAGGGAAAAAGAAAGAA AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAA___AAAAAGGAAGGAAGGAGGGAAAAAGAAAGAA TTTC T AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89859141..89859372 26863196 MeRIP-seq:(Medium) rs748952060 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_25177874 RMVar_hsa_circ_84501,RMVar_hsa_circ_100602,RMVar_hsa_circ_174707,RMVar_hsa_circ_174708,RMVar_hsa_circ_174709,RMVar_hsa_circ_359072 106836 RMVar_ID_106836 Human_SNP_ID_587143522 m1A Human chr15 - 89859267 89859267 89859267 AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAAGAAAAAAAGGAAGGAAGGAGGGAAAAAGAAAGAA AAAAAGAAAAGAAAAAAGGAAAGAAAGAAAAGGAAAAAAGGAAGGAAGGAGGGAAAAAGAAAGAA T C AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89859141..89859372 26863196 MeRIP-seq:(Medium) rs1274598884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25177874 RMVar_hsa_circ_84501,RMVar_hsa_circ_100602,RMVar_hsa_circ_174707,RMVar_hsa_circ_174708,RMVar_hsa_circ_174709,RMVar_hsa_circ_359072 106837 RMVar_ID_106837 Human_SNP_ID_587154132 m1A Human chr15 - 89899856 89899856 89899856 AATGGGGGCTGGTGTTTGAGATGAGGCTGGAGATTGGGCATGGCATCCTCACGCATGTTAAGGAA AATGGGGGCTGGTGTTTGAGATGAGGCTGGAGTTTGGGCATGGCATCCTCACGCATGTTAAGGAA T A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:89899805..89899938 26863196 MeRIP-seq:(Medium) rs1203352340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6478848,Human_RBP_ID_12634312,Human_RBP_ID_17869040,Human_RBP_ID_23673946 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 106838 RMVar_ID_106838 Human_SNP_ID_587154957 m1A Human chr15 + 89903276 89903276 89903276 TGCTCTCGGATCTCCGCTGCAGCCCCCTTCGAACACTTTTGGGCCATGATGTTGTCTGTCCAGGA TGCTCTCGGATCTCCGCTGCAGCCCCCTTCGAGCACTTTTGGGCCATGATGTTGTCTGTCCAGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:89903165..89903330 26863196 MeRIP-seq:(Medium) rs1023397170 Functional Loss SNV dbSNP153 33..33 33 - - - 106839 RMVar_ID_106839 Human_SNP_ID_587157548 m1A Human chr15 - 89912838 89912838 89912838 CGGCTCTGTGCCGGGGTGCCCGGGCGGTCGGGAGAATGAGCCGCATCTACCACGACGGCGCGCTC CGGCTCTGTGCCGGGGTGCCCGGGCGGTCGGGGGAATGAGCCGCATCTACCACGACGGCGCGCTC T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89912788..89912894 26863196 MeRIP-seq:(Medium) rs1218680481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343406,Human_RBP_ID_22497022 Human_Splice_Rec_1643459,Human_Splice_Rec_1643503 106840 RMVar_ID_106840 Human_SNP_ID_587157599 m1A Human chr15 + 89912921 89912921 89912921 GCGGCGCGGGAAGTGCTGCAGGACGCGCGGGGACCCGCGATTCCCAGCCGGCGGATCCGGGAATG GCGGCGCGGGAAGTGCTGCAGGACGCGCGGGGGCCCGCGATTCCCAGCCGGCGGATCCGGGAATG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:89912837..89912922 26863410 MeRIP-seq:(Medium) rs568886297 Functional Loss SNV dbSNP153 33..33 33 - - - 106841 RMVar_ID_106841 Human_SNP_ID_587157600 m1A Human chr15 + 89912921 89912921 89912921 GCGGCGCGGGAAGTGCTGCAGGACGCGCGGGGACCCGCGATTCCCAGCCGGCGGATCCGGGAATG GCGGCGCGGGAAGTGCTGCAGGACGCGCGGGGTCCCGCGATTCCCAGCCGGCGGATCCGGGAATG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:89912837..89912922 26863410 MeRIP-seq:(Medium) rs568886297 Functional Loss SNV dbSNP153 33..33 33 - - - 106842 RMVar_ID_106842 Human_SNP_ID_182860640 m1A Human chr4 + 47485377 47485377 47485377 TGGCTCCCGCAGCTGAGTTTGGGAGATGTCTAAGTGATTTTTTTTTTTTCCCGGAAGGCAAATGG TGGCTCCCGCAGCTGAGTTTGGGAGATGTCTACGTGATTTTTTTTTTTTCCCGGAAGGCAAATGG A C ATP10D Ensembl:ENSG00000145246 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:47485327..47485396 26863196 MeRIP-seq:(Medium) rs1461135854 Functional Loss SNV dbSNP153 33..33 33 - - - 106843 RMVar_ID_106843 Human_SNP_ID_183057221 m1A Human chr4 - 48342032 48342032 48342032 CCTCGTCCAGCAAGCCGCCCTCGCCCGCCGCTAGCAAGGAGGTGGCGTCCCGCAGCTCTTCGCTA CCTCGTCCAGCAAGCCGCCCTCGCCCGCCGCTTGCAAGGAGGTGGCGTCCCGCAGCTCTTCGCTA T A lnc-TEC-2,lnc-TEC-2:2 RNACentral:URS0000D58AF2,RNACentral:URS00009AE996 lincRNA,lincRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:48341985..48342139 26863196 MeRIP-seq:(Medium) rs1337424179 Functional Loss SNV dbSNP153 33..33 33 - - - 106844 RMVar_ID_106844 Human_SNP_ID_183142655 m1A Human chr4 - 48710695 48710695 48710695 ACCATATTTCCTATTTTTTAATCTTCCAGCCTAGAACATTCCATATTCTGCTTCACACACGGTGA ACCATATTTCCTATTTTTTAATCTTCCAGCCTGGAACATTCCATATTCTGCTTCACACACGGTGA T C FRYL Ensembl:ENSG00000075539 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:48710604..48727437 26863196 MeRIP-seq:(Medium) rs1009744991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_559406,Human_Splice_Rec_559596,Human_Splice_Rec_559884,Human_Splice_Rec_560040,Human_Splice_Rec_560058 Human_miRNA_ID_1933080,Human_miRNA_ID_2196887,Human_miRNA_ID_2935892 RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_84281,RMVar_hsa_circ_225958,RMVar_hsa_circ_93802,RMVar_hsa_circ_225962,RMVar_hsa_circ_24962,RMVar_hsa_circ_2546,RMVar_hsa_circ_225970,RMVar_hsa_circ_225971,RMVar_hsa_circ_276310,RMVar_hsa_circ_358340,RMVar_hsa_circ_100943,RMVar_hsa_circ_225979,RMVar_hsa_circ_225977,RMVar_hsa_circ_225978,RMVar_hsa_circ_225976,RMVar_hsa_circ_103285,RMVar_hsa_circ_337869,RMVar_hsa_circ_297780,RMVar_hsa_circ_225980 106845 RMVar_ID_106845 Human_SNP_ID_183171437 m1A Human chr4 + 48831178 48831178 48831178 CTTGCACTTTTCTCCCTCCCTGCCCCCTCTCGAGTCCACCCTCCGGGCCTTCTGCCCCTGATCGC CTTGCACTTTTCTCCCTCCCTGCCCCCTCTCGGGTCCACCCTCCGGGCCTTCTGCCCCTGATCGC A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:48831128..48831526 32194978 MeRIP-seq:(Medium) rs1486827287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_621626,Human_RBP_ID_786943,Human_RBP_ID_18955551,Human_RBP_ID_27841837 Human_Splice_Rec_560123,Human_Splice_Rec_560141,Human_Splice_Rec_560161,Human_Splice_Rec_560177,Human_Splice_Rec_560211,Human_Splice_Rec_560239,Human_Splice_Rec_560253,Human_Splice_Rec_560263,Human_Splice_Rec_560271,Human_Splice_Rec_560281,Human_Splice_Rec_560303,Human_Splice_Rec_560311 106846 RMVar_ID_106846 Human_SNP_ID_183171445 m1A Human chr4 - 48831198 48831198 48831198 GCGACTGCAAGGAAAACCAAGCGATCAGGGGCAGAAGGCCCGGAGGGTGGACTCGAGAGGGGGCA GCGACTGCAAGGAAAACCAAGCGATCAGGGGCCGAAGGCCCGGAGGGTGGACTCGAGAGGGGGCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:48831151..48831275 32194978 MeRIP-seq:(Medium) rs1340074599 Functional Loss SNV dbSNP153 33..33 33 - - - 106847 RMVar_ID_106847 Human_SNP_ID_183171810 m1A Human chr4 + 48832676 48832676 48832676 TTCGAGAGCCGAATGCAGAGGTTCCAAGACCAATTCCCCGTAACTATCTATTAAGTATTTATAAT TTCGAGAGCCGAATGCAGAGGTTCCAAGACCAGTTCCCCGTAACTATCTATTAAGTATTTATAAT A G OCIAD1 Ensembl:ENSG00000109180 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:48831079..48832713 26863196 MeRIP-seq:(Medium) rs1162952555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248864,Human_RBP_ID_19122505,Human_RBP_ID_22458579 Human_Splice_Rec_560066,Human_Splice_Rec_560067,Human_Splice_Rec_560076,Human_Splice_Rec_560077,Human_Splice_Rec_560092,Human_Splice_Rec_560093,Human_Splice_Rec_560100,Human_Splice_Rec_560101,Human_Splice_Rec_560114,Human_Splice_Rec_560115,Human_Splice_Rec_560136,Human_Splice_Rec_560137,Human_Splice_Rec_560142,Human_Splice_Rec_560143,Human_Splice_Rec_560152,Human_Splice_Rec_560153,Human_Splice_Rec_560162,Human_Splice_Rec_560163,Human_Splice_Rec_560178,Human_Splice_Rec_560179,Human_Splice_Rec_560192,Human_Splice_Rec_560193,Human_Splice_Rec_560204,Human_Splice_Rec_560205,Human_Splice_Rec_560212,Human_Splice_Rec_560213,Human_Splice_Rec_560224,Human_Splice_Rec_560225,Human_Splice_Rec_560240,Human_Splice_Rec_560241,Human_Splice_Rec_560254,Human_Splice_Rec_560255,Human_Splice_Rec_560294,Human_Splice_Rec_560295,Human_Splice_Rec_560304,Human_Splice_Rec_560305,Human_Splice_Rec_560312,Human_Splice_Rec_560313,Human_Splice_Rec_560324,Human_Splice_Rec_560325,Human_Splice_Rec_560338,Human_Splice_Rec_560339,Human_Splice_Rec_560354,Human_Splice_Rec_560355 RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_375987,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_225984,RMVar_hsa_circ_225982 106848 RMVar_ID_106848 Human_SNP_ID_183189849 m1A Human chr4 - 48906719 48906719 48906719 GCTGGAGCGGGCCGGCGGTGCAGTCACGGGGGAGCGAGGCCTGCTGGGCTTGGCAACGAGGGACT GCTGGAGCGGGCCGGCGGTGCAGTCACGGGGGTGCGAGGCCTGCTGGGCTTGGCAACGAGGGACT T A OCIAD2 Ensembl:ENSG00000145247 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:48904576..48906788 26863196 MeRIP-seq:(Medium) rs1371131074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_560375,Human_Splice_Rec_560387,Human_Splice_Rec_560397,Human_Splice_Rec_560407,Human_Splice_Rec_560417,Human_Splice_Rec_560427,Human_Splice_Rec_560433,Human_Splice_Rec_560447 106849 RMVar_ID_106849 Human_SNP_ID_183240698 m1A Human chr4 + 49091310 49091310 49091310 CTACACGGGTTGATTCCATTCCATTCCATTCCATTCCATTCCAGTCGTGTTGATACCATTCCATT CTACACGGGTTGATTCCATTCCATTCCATTCCGTTCCATTCCAGTCGTGTTGATACCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49091255..49091388 26863196 MeRIP-seq:(Medium) rs1479575732 Functional Loss SNV dbSNP153 33..33 33 - - - 106850 RMVar_ID_106850 Human_SNP_ID_183241480 m1A Human chr4 - 49092528 49092528 49092528 GATTGGAAAGGAACGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAGTG GATTGGAAAGGAACGGAATGGAATGGAATGGAGTGGAATGGAATGGAATGGAATGGAATGGAGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49092482..49092566 26863196 MeRIP-seq:(Medium) rs990769223 Functional Loss SNV dbSNP153 33..33 33 - - - 106851 RMVar_ID_106851 Human_SNP_ID_183241718 m1A Human chr4 - 49092882 49092882 49092882 AATGGAATGGAATGGAATGGAGTGGAATCAACACGAATGGAAAGGAACGGAATGGAATGGAATGC AATGGAATGGAATGGAATGGAGTGGAATCAACGCGAATGGAAAGGAACGGAATGGAATGGAATGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49092817..49092946 26863196 MeRIP-seq:(Medium) rs371292158 Functional Loss SNV dbSNP153 33..33 33 - - - 106852 RMVar_ID_106852 Human_SNP_ID_183241719 m1A Human chr4 - 49092882 49092882 49092882 AATGGAATGGAATGGAATGGAGTGGAATCAACACGAATGGAAAGGAACGGAATGGAATGGAATGC AATGGAATGGAATGGAATGGAGTGGAATCAACCCGAATGGAAAGGAACGGAATGGAATGGAATGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49092817..49092946 26863196 MeRIP-seq:(Medium) rs371292158 Functional Loss SNV dbSNP153 33..33 33 - - - 106853 RMVar_ID_106853 Human_SNP_ID_183244774 m1A Human chr4 - 49096430 49096430 49096430 GGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAACGGAATGGAATCCAACGGAAT GGAATGGAATGGAATGGAATGGAATGGAATGGGATGGAATGGAACGGAATGGAATCCAACGGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49096354..49096486 26863196 MeRIP-seq:(Medium) rs1004366774 Functional Loss SNV dbSNP153 33..33 33 - - - 106854 RMVar_ID_106854 Human_SNP_ID_183245872 m1A Human chr4 - 49098157 49098157 49098157 GGAATGGAATGGAATGGAATAGAAACAACACGAATGGAATGGAACAGAACGGAATGGAAAGGAAT GGAATGGAATGGAATGGAATAGAAACAACACGTATGGAATGGAACAGAACGGAATGGAAAGGAAT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49097985..49098232 26863196 MeRIP-seq:(Medium) rs982186151 Functional Loss SNV dbSNP153 33..33 33 - - - 106855 RMVar_ID_106855 Human_SNP_ID_183246212 m1A Human chr4 - 49098571 49098571 49098571 GGAACGGAACGGAACGGAATGGAATGGAATGGAATGGAATGGGATGGAATGGAATGGAATGGAAT GGAACGGAACGGAACGGAATGGAATGGAATGGGATGGAATGGGATGGAATGGAATGGAATGGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49098521..49098671 26863196 MeRIP-seq:(Medium) rs553779556 Functional Loss SNV dbSNP153 33..33 33 - - - 106856 RMVar_ID_106856 Human_SNP_ID_183246374 m1A Human chr4 + 49098823 49098823 49098823 CCATTCCATTTCATTCCATTCCTTTCCATTCCATTCCACTCGGGTTGATTCCGTTGCATTCCATT CCATTCCATTTCATTCCATTCCTTTCCATTCCCTTCCACTCGGGTTGATTCCGTTGCATTCCATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49098811..49098898 26863196 MeRIP-seq:(Medium) rs1057029391 Functional Loss SNV dbSNP153 33..33 33 - - - 106857 RMVar_ID_106857 Human_SNP_ID_183246375 m1A Human chr4 + 49098823 49098823 49098823 CCATTCCATTTCATTCCATTCCTTTCCATTCCATTCCACTCGGGTTGATTCCGTTGCATTCCATT CCATTCCATTTCATTCCATTCCTTTCCATTCCGTTCCACTCGGGTTGATTCCGTTGCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49098811..49098898 26863196 MeRIP-seq:(Medium) rs1057029391 Functional Loss SNV dbSNP153 33..33 33 - - - 106858 RMVar_ID_106858 Human_SNP_ID_183246376 m1A Human chr4 + 49098823 49098823 49098823 CCATTCCATTTCATTCCATTCCTTTCCATTCCATTCCACTCGGGTTGATTCCGTTGCATTCCATT CCATTCCATTTCATTCCATTCCTTTCCATTCCTTTCCACTCGGGTTGATTCCGTTGCATTCCATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49098811..49098898 26863196 MeRIP-seq:(Medium) rs1057029391 Functional Loss SNV dbSNP153 33..33 33 - - - 106859 RMVar_ID_106859 Human_SNP_ID_183247164 m1A Human chr4 - 49100011 49100007 49100012 CGAATGCAATGGAATGGAATGGAATGGAATCAACCCGAATGGGATGGAATGGAATGGAATGGAAT CGAATGCAATGGAATGGAATGGAATGGAATC_____GAATGGGATGGAATGGAATGGAATGGAAT CGGGTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49099975..49100355 26863196 MeRIP-seq:(Medium) rs369393774 Functional Loss DEL dbSNP153 32..36 33 - - - 106860 RMVar_ID_106860 Human_SNP_ID_183248888 m1A Human chr4 - 49102352 49102347 49102352 GAATGGAATGGAATGGAATGGAATGGAATGGAATGGAGTGGAATGGAATGGAATCCACCCGAGTG GAATGGAATGGAATGGAATGGAATGGAATGGA_____GTGGAATGGAATGGAATCCACCCGAGTG CTCCAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49102301..49102405 26863196 MeRIP-seq:(Medium) rs61728464 Functional Loss DEL dbSNP153 33..37 33 - - - 106861 RMVar_ID_106861 Human_SNP_ID_183249135 m1A Human chr4 + 49102721 49102721 49102721 CCATTCCACTCGGGTTGATTCCATTCCATTCCATTCCATTCCACTCCATTCCATTCCATTCCTTT CCATTCCACTCGGGTTGATTCCATTCCATTCCGTTCCATTCCACTCCATTCCATTCCATTCCTTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49102549..49102790 26863196 MeRIP-seq:(Medium) rs1164771452 Functional Loss SNV dbSNP153 33..33 33 - - - 106862 RMVar_ID_106862 Human_SNP_ID_183249136 m1A Human chr4 + 49102721 49102721 49102721 CCATTCCACTCGGGTTGATTCCATTCCATTCCATTCCATTCCACTCCATTCCATTCCATTCCTTT CCATTCCACTCGGGTTGATTCCATTCCATTCCTTTCCATTCCACTCCATTCCATTCCATTCCTTT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49102549..49102790 26863196 MeRIP-seq:(Medium) rs1164771452 Functional Loss SNV dbSNP153 33..33 33 - - - 106863 RMVar_ID_106863 Human_SNP_ID_183250616 m1A Human chr4 - 49104698 49104698 49104698 GAAATAAACACGAATAGAATGGAATGGAATGGAATGGAAAGGAAAGGAATGCAATGCAATGGAAT GAAATAAACACGAATAGAATGGAATGGAATGGGATGGAAAGGAAAGGAATGCAATGCAATGGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49104696..49104848 26863196 MeRIP-seq:(Medium) rs1456052053 Functional Loss SNV dbSNP153 33..33 33 - - - 106864 RMVar_ID_106864 Human_SNP_ID_183252478 m1A Human chr4 + 49107450 49107450 49107450 CCTTTCCATTCCATTCCAATGCATTCCCTTCCATTCAATTCCACTCGGATTCAATCAATTCCATT CCTTTCCATTCCATTCCAATGCATTCCCTTCCGTTCAATTCCACTCGGATTCAATCAATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49107367..49107502 26863196 MeRIP-seq:(Medium) rs1384750108 Functional Loss SNV dbSNP153 33..33 33 - - - 106865 RMVar_ID_106865 Human_SNP_ID_183252745 m1A Human chr4 - 49107851 49107850 49107851 GAATGGAGTGGAATGGAATGGAATGGAATGGAATGGAATCAACACGAAAGGAATGGAACGGAATG GAATGGAGTGGAATGGAATGGAATGGAATGGA_TGGAATCAACACGAAAGGAATGGAACGGAATG AT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49107750..49107924 26863196 MeRIP-seq:(Medium) rs1365880222 Functional Loss DEL dbSNP153 33..33 33 - - - 106866 RMVar_ID_106866 Human_SNP_ID_183253919 m1A Human chr4 - 49109513 49109513 49109513 GAATGGAATGGAATGGAATCCACCCGAGTGGAATGGAATGGAATGGAATGCAATGGAATTGAACG GAATGGAATGGAATGGAATCCACCCGAGTGGATTGGAATGGAATGGAATGCAATGGAATTGAACG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49109501..49109593 26863196 MeRIP-seq:(Medium) rs1560541343 Functional Loss SNV dbSNP153 33..33 33 - - - 106867 RMVar_ID_106867 Human_SNP_ID_183254595 m1A Human chr4 - 49110445 49110419 49110446 TTAATGGAGTGGAATGGAATGGAATGGAATGGAATGGAATGGAACGGAATGGAATGGAATGGAAT TTAATGGAGTGGAATGGAATGGAATGGAATG___________________________ATGGAAT TTCCATTCCATTCCGTTCCATTCCATTC T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49110434..49110620 26863196 MeRIP-seq:(Medium) rs1242212494 Functional Loss DEL dbSNP153 32..58 33 - - - 106868 RMVar_ID_106868 Human_SNP_ID_183256878 m1A Human chr4 - 49113788 49113774 49113789 CGAGTGGAATGGAATGGAATGGAATGGAATGCAATGGAATGGAATGGAATGGAATGGAATGGAAT CGAGTGGAATGGAATGGAATGGAATGGAATG_______________GAATGGAATGGAATGGAAT CCATTCCATTCCATTG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49113771..49113887 26863196 MeRIP-seq:(Medium) rs1316650621 Functional Loss DEL dbSNP153 32..46 33 - - - 106869 RMVar_ID_106869 Human_SNP_ID_183257620 m1A Human chr4 - 49114766 49114766 49114766 GAATGGAATGGAATGGAACGGAACGGAATGGAATGGAATGCAATGGAATGGAATCTACCCGAGTG GAATGGAATGGAATGGAACGGAACGGAATGGAGTGGAATGCAATGGAATGGAATCTACCCGAGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49114753..49114848 26863196 MeRIP-seq:(Medium) rs908540570 Functional Loss SNV dbSNP153 33..33 33 - - - 106870 RMVar_ID_106870 Human_SNP_ID_183258887 m1A Human chr4 - 49116632 49116630 49116632 GAATCAACCCGAGAGGAATGAAATGGAATGGAATGGAATGGAATGGAATGGAATGGCAATGAATA GAATCAACCCGAGAGGAATGAAATGGAATGGA__GGAATGGAATGGAATGGAATGGCAATGAATA CAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49116618..49116717 26863196 MeRIP-seq:(Medium) rs1326470220 Functional Loss DEL dbSNP153 33..34 33 - - - 106871 RMVar_ID_106871 Human_SNP_ID_183259262 m1A Human chr4 + 49117166 49117166 49117166 CCATTCCATTCCATTCCATACCATTCCACAAAAGTTGATTGCATGTTATTCCATTCCATTCCATT CCATTCCATTCCATTCCATACCATTCCACAAACGTTGATTGCATGTTATTCCATTCCATTCCATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49117158..49117360 26863196 MeRIP-seq:(Medium) rs1461292043 Functional Loss SNV dbSNP153 33..33 33 - - - 106872 RMVar_ID_106872 Human_SNP_ID_183259263 m1A Human chr4 + 49117166 49117166 49117166 CCATTCCATTCCATTCCATACCATTCCACAAAAGTTGATTGCATGTTATTCCATTCCATTCCATT CCATTCCATTCCATTCCATACCATTCCACAAATGTTGATTGCATGTTATTCCATTCCATTCCATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49117158..49117360 26863196 MeRIP-seq:(Medium) rs1461292043 Functional Loss SNV dbSNP153 33..33 33 - - - 106873 RMVar_ID_106873 Human_SNP_ID_183259900 m1A Human chr4 - 49118170 49118170 49118170 GAAAGGAATTAACCCGAAGGGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATTAACCC GAAAGGAATTAACCCGAAGGGAATGGAATGGACTGGAATGGAAAGGAATGGAATGGAATTAACCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49118152..49118237 26863196 MeRIP-seq:(Medium) rs1396294968 Functional Loss SNV dbSNP153 33..33 33 - - - 106874 RMVar_ID_106874 Human_SNP_ID_183260158 m1A Human chr4 - 49118563 49118543 49118563 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATCAACTCGAAGGGAATGGAATGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAA____________________TGGAATGGAATGG ATTCCCTTCGAGTTGATTCCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49118561..49118752 26863196 MeRIP-seq:(Medium) rs1351412379 Functional Loss DEL dbSNP153 33..52 33 - - - 106875 RMVar_ID_106875 Human_SNP_ID_183260170 m1A Human chr4 - 49118563 49118558 49118563 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATCAACTCGAAGGGAATGGAATGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAA_____TCAACTCGAAGGGAATGGAATGGAATGG ATTCCT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49118561..49118752 26863196 MeRIP-seq:(Medium) rs1560545676 Functional Loss DEL dbSNP153 33..37 33 - - - 106876 RMVar_ID_106876 Human_SNP_ID_183260175 m1A Human chr4 - 49118563 49118563 49118563 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATCAACTCGAAGGGAATGGAATGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATCAACTCGAAGGGAATGGAATGGAATGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49118561..49118752 26863196 MeRIP-seq:(Medium) rs201173269 Functional Loss SNV dbSNP153 33..33 33 - - - 106877 RMVar_ID_106877 Human_SNP_ID_183276497 m1A Human chr4 - 49134221 49134221 49134221 GGAATGGAAATGAATCAAATCAAGTGGAATGGAATGGAATGGAATTTAATGGAATGGAATGGAAA GGAATGGAAATGAATCAAATCAAGTGGAATGGTATGGAATGGAATTTAATGGAATGGAATGGAAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49134162..49134268 26863196 MeRIP-seq:(Medium) rs1397629442 Functional Loss SNV dbSNP153 33..33 33 - - - 106878 RMVar_ID_106878 Human_SNP_ID_183276498 m1A Human chr4 - 49134221 49134221 49134221 GGAATGGAAATGAATCAAATCAAGTGGAATGGAATGGAATGGAATTTAATGGAATGGAATGGAAA GGAATGGAAATGAATCAAATCAAGTGGAATGGGATGGAATGGAATTTAATGGAATGGAATGGAAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49134162..49134268 26863196 MeRIP-seq:(Medium) rs1397629442 Functional Loss SNV dbSNP153 33..33 33 - - - 106879 RMVar_ID_106879 Human_SNP_ID_183276499 m1A Human chr4 - 49134221 49134221 49134221 GGAATGGAAATGAATCAAATCAAGTGGAATGGAATGGAATGGAATTTAATGGAATGGAATGGAAA GGAATGGAAATGAATCAAATCAAGTGGAATGGCATGGAATGGAATTTAATGGAATGGAATGGAAA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49134162..49134268 26863196 MeRIP-seq:(Medium) rs1397629442 Functional Loss SNV dbSNP153 33..33 33 - - - 106880 RMVar_ID_106880 Human_SNP_ID_183284347 m1A Human chr4 - 49141100 49141100 49141100 GGAACGGAATTGAATGGAGTGGAATCAACCCGAGCGGAAAGGAATGGAATGGAATGGAATGGAAT GGAACGGAATTGAATGGAGTGGAATCAACCCGGGCGGAAAGGAATGGAATGGAATGGAATGGAAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49141050..49141163 26863196 MeRIP-seq:(Medium) rs1459698184 Functional Loss SNV dbSNP153 33..33 33 - - - 106881 RMVar_ID_106881 Human_SNP_ID_183287351 m1A Human chr4 + 49144600 49144600 49144600 CCGTTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTGCATTCCATACCATTCCATT CCGTTCCATTCCATTCCATTCCATTCCATTCCGTTCCATTCCATTGCATTCCATACCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49144514..49144883 26863196 MeRIP-seq:(Medium) rs796867314 Functional Loss SNV dbSNP153 33..33 33 - - - 106882 RMVar_ID_106882 Human_SNP_ID_183288059 m1A Human chr4 + 49145542 49145542 49145542 CCATTCTATTCCATTCCATTCCATTAAATTCCATTCCATTCCATTCCACTCGTGTAGATTCCATT CCATTCTATTCCATTCCATTCCATTAAATTCCTTTCCATTCCATTCCACTCGTGTAGATTCCATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49145466..49145608 26863196 MeRIP-seq:(Medium) rs1244498924 Functional Loss SNV dbSNP153 33..33 33 - - - 106883 RMVar_ID_106883 Human_SNP_ID_183289756 m1A Human chr4 + 49148112 49148112 49148112 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCTTTCCACTCGGGTTGATTACATT CCATTCCATTCCATTCCATTCCATTCCATTCCCTTCCATTCCTTTCCACTCGGGTTGATTACATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49148097..49148229 26863196 MeRIP-seq:(Medium) rs1000856853 Functional Loss SNV dbSNP153 33..33 33 - - - 106884 RMVar_ID_106884 Human_SNP_ID_183290670 m1A Human chr4 + 49149392 49149392 49149392 CACTCGGGTTGATTACATTCCATTCCATTCCAATCCATTCCATTCCATTCCATTCCATTCCATTC CACTCGGGTTGATTACATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49149265..49149427 26863196 MeRIP-seq:(Medium) rs200153971 Functional Loss SNV dbSNP153 33..33 33 - - - 106885 RMVar_ID_106885 Human_SNP_ID_183291736 m1A Human chr4 + 49151034 49151034 49151034 TCCATTCCATTCCATTCCACTCGGGTTGATTCAATTCCGTTCCTTTCCATTCCATTCCATTCTAT TCCATTCCATTCCATTCCACTCGGGTTGATTCCATTCCGTTCCTTTCCATTCCATTCCATTCTAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49150870..49151040 26863196 MeRIP-seq:(Medium) rs61794768 Functional Loss SNV dbSNP153 33..33 33 - - - 106886 RMVar_ID_106886 Human_SNP_ID_183291737 m1A Human chr4 + 49151034 49151034 49151034 TCCATTCCATTCCATTCCACTCGGGTTGATTCAATTCCGTTCCTTTCCATTCCATTCCATTCTAT TCCATTCCATTCCATTCCACTCGGGTTGATTCTATTCCGTTCCTTTCCATTCCATTCCATTCTAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49150870..49151040 26863196 MeRIP-seq:(Medium) rs61794768 Functional Loss SNV dbSNP153 33..33 33 - - - 106887 RMVar_ID_106887 Human_SNP_ID_183292909 m1A Human chr4 + 49152816 49152816 49152816 CCGTTTCATTCCGTTGCATTCCACTCGGGTTGATTCCATTACTTTCCATTCCATTCCATTCCATT CCGTTTCATTCCGTTGCATTCCACTCGGGTTGGTTCCATTACTTTCCATTCCATTCCATTCCATT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49152794..49153042 26863196 MeRIP-seq:(Medium) rs1181772952 Functional Loss SNV dbSNP153 33..33 33 - - - 106888 RMVar_ID_106888 Human_SNP_ID_183293713 m1A Human chr4 - 49154179 49154175 49154180 GGAATGGAATGGAATGGAATGGAATGGAATCAACCAGAGTGGAATGGAAAGGAGTAGAATGGAAT GGAATGGAATGGAATGGAATGGAATGGAATC_____GAGTGGAATGGAAAGGAGTAGAATGGAAT CTGGTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49154159..49154276 26863196 MeRIP-seq:(Medium) rs372265090 Functional Loss DEL dbSNP153 32..36 33 - - - 106889 RMVar_ID_106889 Human_SNP_ID_183297102 m1A Human chr4 + 49161531 49161531 49161531 GGCGGGGGCTGGGAGGACAGGCGTGGGGTCCCAGCAGTGACGCGGGTTCTAGAGGCACAGGAGCG GGCGGGGGCTGGGAGGACAGGCGTGGGGTCCCGGCAGTGACGCGGGTTCTAGAGGCACAGGAGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:49161482..49161565 26863196 MeRIP-seq:(Medium) rs1322868412 Functional Loss SNV dbSNP153 33..33 33 - - - 106890 RMVar_ID_106890 Human_SNP_ID_183383023 m1A Human chr4 - 49487015 49487015 49487015 AGCAGGTGAAATATTTTCTCAGCACTCTTCCTACAAGGCGAGGTCGAGAGTCACCTTGTGTTGAA AGCAGGTGAAATATTTTCTCAGCACTCTTCCTGCAAGGCGAGGTCGAGAGTCACCTTGTGTTGAA T C AC119751.3 Ensembl:ENSG00000248583 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28970566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124201 Human_Splice_Rec_560558 106891 RMVar_ID_106891 Human_SNP_ID_183397141 m1A Human chr4 + 49510607 49510607 49510607 TTCTCTCTTACTCCTTCTGCCCTCTCTCTTTCATATGCCTTAGGTGCATCCCACATTCTGCGTTT TTCTCTCTTACTCCTTCTGCCCTCTCTCTTTCCTATGCCTTAGGTGCATCCCACATTCTGCGTTT A C HSALNG0034347-001 RNACentral:URS0000EBF1A5 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2313294 Functional Loss SNV dbSNP153 33..33 33 - - - 106892 RMVar_ID_106892 Human_SNP_ID_183435623 m1A Human chr4 + 49578042 49578042 49578042 AGGGTGTGGTCAGGGAGGAAGTGATATGCTGGATCTGGTCACCAGGGACCTGGTCAATGGGGGCT AGGGTGTGGTCAGGGAGGAAGTGATATGCTGGTTCTGGTCACCAGGGACCTGGTCAATGGGGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:49577992..49578082 26863196 MeRIP-seq:(Medium) rs1560407538 Functional Loss SNV dbSNP153 33..33 33 - - - 106893 RMVar_ID_106893 Human_SNP_ID_183472581 m1A Human chr4 + 49631433 49631432 49631434 TGGATGGAATGGAATGGAATGGAATGGAATGGAATTGAATGGAATGGATTGGAATGGAATGGAAT TGGATGGAATGGAATGGAATGGAATGGAATGG__TTGAATGGAATGGATTGGAATGGAATGGAAT GAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49631383..49631473 26863196 MeRIP-seq:(Medium) rs1560432753 Functional Loss DEL dbSNP153 33..34 33 - - - 106894 RMVar_ID_106894 Human_SNP_ID_183472582 m1A Human chr4 + 49631433 49631433 49631433 TGGATGGAATGGAATGGAATGGAATGGAATGGAATTGAATGGAATGGATTGGAATGGAATGGAAT TGGATGGAATGGAATGGAATGGAATGGAATGGCATTGAATGGAATGGATTGGAATGGAATGGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49631383..49631473 26863196 MeRIP-seq:(Medium) rs1170391263 Functional Loss SNV dbSNP153 33..33 33 - - - 106895 RMVar_ID_106895 Human_SNP_ID_183473824 m1A Human chr4 - 49632958 49632958 49632958 CCTTTCCATTCCAATCGGGTTGATTCCATTCCATTCCATTCCATTCCATTCCATTCCGTTCCACT CCTTTCCATTCCAATCGGGTTGATTCCATTCCGTTCCATTCCATTCCATTCCATTCCGTTCCACT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49632864..49633003 26863196 MeRIP-seq:(Medium) rs1456038775 Functional Loss SNV dbSNP153 33..33 33 - - - 106896 RMVar_ID_106896 Human_SNP_ID_183474607 m1A Human chr4 + 49633954 49633954 49633954 GAATGTAATGGAATGTAATGGAATGGAATGGAATGGAATGCAATGGAATGGAATGCAATGGAATG GAATGTAATGGAATGTAATGGAATGGAATGGATTGGAATGCAATGGAATGGAATGCAATGGAATG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49633903..49633992 26863196 MeRIP-seq:(Medium) rs957695144 Functional Loss SNV dbSNP153 33..33 33 - - - 106897 RMVar_ID_106897 Human_SNP_ID_183475853 m1A Human chr4 + 49635526 49635526 49635526 TGAATGGAATGGAATCAACACGAGTGGAAAGGAATGGAATGGAATGGAATGGAATGGAATGGAAT TGAATGGAATGGAATCAACACGAGTGGAAAGGCATGGAATGGAATGGAATGGAATGGAATGGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49635476..49635584 26863196 MeRIP-seq:(Medium) rs796542969 Functional Loss SNV dbSNP153 33..33 33 - - - 106898 RMVar_ID_106898 Human_SNP_ID_183477320 m1A Human chr4 + 49637108 49637108 49637108 GGAATGGAAAGCAATGGAATGGAATGAACCCGAGTGGAATGGAATGGAATGGAATGGAATGGAAT GGAATGGAAAGCAATGGAATGGAATGAACCCGTGTGGAATGGAATGGAATGGAATGGAATGGAAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49637096..49637181 26863196 MeRIP-seq:(Medium) rs200849427 Functional Loss SNV dbSNP153 33..33 33 - - - 106899 RMVar_ID_106899 Human_SNP_ID_183478199 m1A Human chr4 + 49638318 49638318 49638318 TGGTGGAATGGTATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGCAATCAACTGGAATG TGGTGGAATGGTATGGAATGGAATGGAATGGATTGGAATGGAATGGAATGCAATCAACTGGAATG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49638300..49638428 26863196 MeRIP-seq:(Medium) rs1433658457 Functional Loss SNV dbSNP153 33..33 33 - - - 106900 RMVar_ID_106900 Human_SNP_ID_183479233 m1A Human chr4 - 49639442 49639442 49639442 TCCATTCCACTCATGTTGATTCCATTCTTTCCATTCCATTCCATTCCATTCCATTCCATTCCATT TCCATTCCACTCATGTTGATTCCATTCTTTCCTTTCCATTCCATTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49639377..49639473 26863196 MeRIP-seq:(Medium) rs868047435 Functional Loss SNV dbSNP153 33..33 33 - - - 106901 RMVar_ID_106901 Human_SNP_ID_183480167 m1A Human chr4 + 49640567 49640567 49640567 TAACTGGAGTGGAATGGAATGTAATGGAATGCAGTGGAATGGAATGGAACGGAATGGAATGGAAT TAACTGGAGTGGAATGGAATGTAATGGAATGCGGTGGAATGGAATGGAACGGAATGGAATGGAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49640561..49640664 26863196 MeRIP-seq:(Medium) rs547542290 Functional Loss SNV dbSNP153 33..33 33 - - - 106902 RMVar_ID_106902 Human_SNP_ID_183480402 m1A Human chr4 + 49640904 49640904 49640904 ATTGGAATGGTGTGGAATGGAATGGAATGGAAAGGAATCAACTCGAAGGCTATGGAATGGAATGG ATTGGAATGGTGTGGAATGGAATGGAATGGAATGGAATCAACTCGAAGGCTATGGAATGGAATGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49640892..49640976 26863196 MeRIP-seq:(Medium) rs143122018 Functional Loss SNV dbSNP153 33..33 33 - - - 106903 RMVar_ID_106903 Human_SNP_ID_183481140 m1A Human chr4 - 49641854 49641854 49641854 TTATTCCAATCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCACT TTATTCCAATCCATTCCATTCCATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCACT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49641770..49641889 26863196 MeRIP-seq:(Medium) rs796550315 Functional Loss SNV dbSNP153 33..33 33 - - - 106904 RMVar_ID_106904 Human_SNP_ID_183482457 m1A Human chr4 - 49643589 49643589 49643589 CCATTCCATTCCATTGCATTGCATTTCCTTCCATTCCAGTTGATTCCATTCCATTCCATTCCATT CCATTCCATTCCATTGCATTGCATTTCCTTCCTTTCCAGTTGATTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49643575..49643659 26863196 MeRIP-seq:(Medium) rs1344024133 Functional Loss SNV dbSNP153 33..33 33 - - - 106905 RMVar_ID_106905 Human_SNP_ID_183486739 m1A Human chr4 - 49648693 49648683 49648693 CCGTTCCTTTCCATTCCATTCCATTCCATTCCATTCCGTTCCGTTCCATTCCATTCGTGTTGATT CCGTTCCTTTCCATTCCATTCCATTCCATTCC__________GTTCCATTCCATTCGTGTTGATT CGGAACGGAAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49648613..49648770 26863196 MeRIP-seq:(Medium) rs202099456 Functional Loss DEL dbSNP153 33..42 33 - - - 106906 RMVar_ID_106906 Human_SNP_ID_183487977 m1A Human chr4 + 49649936 49649936 49649936 GAGGGAATGGAATGGAACGGAATAGAATGGAAAGGAACGGGACAGAATGGAATGGAATGGAATGG GAGGGAATGGAATGGAACGGAATAGAATGGAATGGAACGGGACAGAATGGAATGGAATGGAATGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49649921..49650099 26863196 MeRIP-seq:(Medium) rs189242714 Functional Loss SNV dbSNP153 33..33 33 - - - 106907 RMVar_ID_106907 Human_SNP_ID_183488525 m1A Human chr4 + 49650574 49650574 49650574 GGAATGGAAAGCAATGGAATGGAATCAACACGAGTGGAATGGAATGGAATGGAAAGGAATGGAAT GGAATGGAAAGCAATGGAATGGAATCAACACGGGTGGAATGGAATGGAATGGAAAGGAATGGAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49650403..49650649 26863196 MeRIP-seq:(Medium) rs1353655194 Functional Loss SNV dbSNP153 33..33 33 - - - 106908 RMVar_ID_106908 Human_SNP_ID_183489201 m1A Human chr4 + 49651369 49651359 49651369 ACCCGAAGGGTATGGAATGGAATATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAAT ACCCGAAGGGTATGGAATGGAAT__________ATGGAATGGAATGGAATGGAATGGAATGGAAT TATGGAATGGA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49651333..49651531 26863196 MeRIP-seq:(Medium) rs200234343 Functional Loss DEL dbSNP153 24..33 33 - - - 106909 RMVar_ID_106909 Human_SNP_ID_183489202 m1A Human chr4 + 49651369 49651359 49651369 ACCCGAAGGGTATGGAATGGAATATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAAT ACCCGAAGGGTATGGAATGGAATATGGA_____ATGGAATGGAATGGAATGGAATGGAATGGAAT TATGGAATGGA TATGGA - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49651333..49651531 26863196 MeRIP-seq:(Medium) rs200234343 Functional Loss DEL dbSNP153 29..33 33 - - - 106910 RMVar_ID_106910 Human_SNP_ID_183490018 m1A Human chr4 - 49652309 49652309 49652309 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTAGGGTCCATTCCATT CCATTCCATTCCATTCCATTCCATTCCATTCCGTTCCATTCCATTCCATTAGGGTCCATTCCATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49652298..49652648 26863196 MeRIP-seq:(Medium) rs1287114518 Functional Loss SNV dbSNP153 33..33 33 - - - 106911 RMVar_ID_106911 Human_SNP_ID_183492703 m1A Human chr4 + 49655494 49655489 49655494 CAATGGAATGGAATGGAATCAACCAGAGTGGAATGGAATGGAATGGAATGGAAAGGAATGGAATG CAATGGAATGGAATGGAATCAACCAGAG_____TGGAATGGAATGGAATGGAAAGGAATGGAATG GTGGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49655470..49655554 26863196 MeRIP-seq:(Medium) rs200966376 Functional Loss DEL dbSNP153 29..33 33 - - - 106912 RMVar_ID_106912 Human_SNP_ID_183492910 m1A Human chr4 + 49655720 49655720 49655720 AATGGATTTTAGTGGAATGGAATGGAATCAACACGAATTGAATGGAACGGAATGGAATGGAATGG AATGGATTTTAGTGGAATGGAATGGAATCAACCCGAATTGAATGGAACGGAATGGAATGGAATGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49655675..49655759 26863196 MeRIP-seq:(Medium) rs142877686 Functional Loss SNV dbSNP153 33..33 33 - - - 106913 RMVar_ID_106913 Human_SNP_ID_183786003 m1A Human chr4 + 51843207 51843207 51843207 AGCTGGTGGGGGGACCGCGAGGCGAGCGCGGGAGCCTGGGCGGCGAGCCGGGTGTGAGCTGCCTG AGCTGGTGGGGGGACCGCGAGGCGAGCGCGGGCGCCTGGGCGGCGAGCCGGGTGTGAGCTGCCTG A C DCUN1D4 Ensembl:ENSG00000109184 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:51843125..51843401 26863196 MeRIP-seq:(Medium) rs993649285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249259,Human_RBP_ID_3747400,Human_RBP_ID_4786733,Human_RBP_ID_9435791,Human_RBP_ID_18424751,Human_RBP_ID_18500966,Human_RBP_ID_19014422 Human_Splice_Rec_560567,Human_Splice_Rec_560583,Human_Splice_Rec_560591,Human_Splice_Rec_560609,Human_Splice_Rec_560619,Human_Splice_Rec_560631,Human_Splice_Rec_560641,Human_Splice_Rec_560649,Human_Splice_Rec_560671,Human_Splice_Rec_560691 106914 RMVar_ID_106914 Human_SNP_ID_183786016 m1A Human chr4 - 51843227 51843227 51843227 GCGGCATCCGAGTGCATTTTCAGGCAGCTCACACCCGGCTCGCCGCCCAGGCTCCCGCGCTCGCC GCGGCATCCGAGTGCATTTTCAGGCAGCTCACTCCCGGCTCGCCGCCCAGGCTCCCGCGCTCGCC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:51843180..51843355 26863196 MeRIP-seq:(Medium) rs548047506 Functional Loss SNV dbSNP153 33..33 33 - - - 106915 RMVar_ID_106915 Human_SNP_ID_183786380 m1A Human chr4 + 51843864 51843864 51843864 GGGGAATGGGGGCAGCGGCCGAGCGGGGCAGGAGGGCGGGCGACTGGACGAGGGCTGATGTAACG GGGGAATGGGGGCAGCGGCCGAGCGGGGCAGGGGGGCGGGCGACTGGACGAGGGCTGATGTAACG A G DCUN1D4 Ensembl:ENSG00000109184 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:51843854..51844066 26863196 MeRIP-seq:(Medium) rs1348441704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3749068,Human_RBP_ID_8211731,Human_RBP_ID_9436231,Human_RBP_ID_18955203,Human_RBP_ID_21988654,Human_RBP_ID_26791600 106916 RMVar_ID_106916 Human_SNP_ID_183786479 m1A Human chr4 - 51844141 51844136 51844142 CCCAACTCCGCCCCACCTCCCCTTCCTCCCCGACTAGCTCCTCACCCCCATTTCATATTCTCCAC CCCAACTCCGCCCCACCTCCCCTTCCTCCCC______CTCCTCACCCCCATTTCATATTCTCCAC GCTAGTC G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:51844139..51844553 26863196 MeRIP-seq:(Medium) rs1553914835 Functional Loss DEL dbSNP153 32..37 33 - - - 106917 RMVar_ID_106917 Human_SNP_ID_183786480 m1A Human chr4 - 51844141 51844141 51844141 CCCAACTCCGCCCCACCTCCCCTTCCTCCCCGACTAGCTCCTCACCCCCATTTCATATTCTCCAC CCCAACTCCGCCCCACCTCCCCTTCCTCCCCGTCTAGCTCCTCACCCCCATTTCATATTCTCCAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:51844139..51844553 26863196 MeRIP-seq:(Medium) rs1452155516 Functional Loss SNV dbSNP153 33..33 33 - - - 106918 RMVar_ID_106918 Human_SNP_ID_183786496 m1A Human chr4 + 51844167 51844167 51844167 AGCTAGTCGGGGAGGAAGGGGAGGTGGGGCGGAGTTGGGCAGGAGGACTGTCACGTCCAGATTCG AGCTAGTCGGGGAGGAAGGGGAGGTGGGGCGGCGTTGGGCAGGAGGACTGTCACGTCCAGATTCG A C DCUN1D4 Ensembl:ENSG00000109184 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:51844164..51844574 26863196 MeRIP-seq:(Medium) rs984383928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266768,Human_RBP_ID_3747404,Human_RBP_ID_8129917,Human_RBP_ID_8211733,Human_RBP_ID_8236305,Human_RBP_ID_8943752,Human_RBP_ID_9435793,Human_RBP_ID_17195904,Human_RBP_ID_18955204,Human_RBP_ID_22526935,Human_RBP_ID_24057708,Human_RBP_ID_26791601 106919 RMVar_ID_106919 Human_SNP_ID_183786561 m1A Human chr4 - 51844302 51844302 51844302 TCCACCTCAGCCCCGCCCCCTCCTCTCTCCGCACCCCGAAGCTTGGACTCCCCCCTTCAAGGGAC TCCACCTCAGCCCCGCCCCCTCCTCTCTCCGCCCCCCGAAGCTTGGACTCCCCCCTTCAAGGGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:51844298..51844469 26863196 MeRIP-seq:(Medium) rs1233849270 Functional Loss SNV dbSNP153 33..33 33 - - - 106920 RMVar_ID_106920 Human_SNP_ID_183841626 m1A Human chr4 + 52033596 52033596 52033596 TTGTGCTCTTTATTGACACTCCTTCTCTCAACAGCCTTCTCACGCATGGACTTCTTTACAGGACC TTGTGCTCTTTATTGACACTCCTTCTCTCAACGGCCTTCTCACGCATGGACTTCTTTACAGGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr4:52033545..52033639;chr4:52033546..52038233 26863196,32194978 MeRIP-seq:(Medium) rs1330370101 Functional Loss SNV dbSNP153 33..33 33 - - - 106921 RMVar_ID_106921 Human_SNP_ID_183842895 m1A Human chr4 - 52038251 52038251 52038251 CTCGGCGGCGGCGGGCGCGGGAAGATGGCGGCAGCGGCGGCGGCGGCTGCAGAACAGGTCTGTGA CTCGGCGGCGGCGGGCGCGGGAAGATGGCGGCGGCGGCGGCGGCGGCTGCAGAACAGGTCTGTGA T C SGCB Ensembl:ENSG00000163069 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:52038184..52038280;chr4:52033515..52038273 26863196 MeRIP-seq:(Medium) rs886043810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_560825,Human_Splice_Rec_560835 106922 RMVar_ID_106922 Human_SNP_ID_183842899 m1A Human chr4 - 52038259 52038257 52038259 GCGGGGAGCTCGGCGGCGGCGGGCGCGGGAAGATGGCGGCAGCGGCGGCGGCGGCTGCAGAACAG GCGGGGAGCTCGGCGGCGGCGGGCGCGGGAAG__GGCGGCAGCGGCGGCGGCGGCTGCAGAACAG CAT C SGCB Ensembl:ENSG00000163069 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:52037996..52038275 26863196 MeRIP-seq:(Medium) rs886042503 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4786818 Human_Splice_Rec_560825,Human_Splice_Rec_560835 Clinvar_Rec_684 106923 RMVar_ID_106923 Human_SNP_ID_183842900 m1A Human chr4 - 52038259 52038259 52038259 GCGGGGAGCTCGGCGGCGGCGGGCGCGGGAAGATGGCGGCAGCGGCGGCGGCGGCTGCAGAACAG GCGGGGAGCTCGGCGGCGGCGGGCGCGGGAAGGTGGCGGCAGCGGCGGCGGCGGCTGCAGAACAG T C SGCB Ensembl:ENSG00000163069 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:52037996..52038275 26863196 MeRIP-seq:(Medium) rs398123262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4786818 Human_Splice_Rec_560825,Human_Splice_Rec_560835 Clinvar_Rec_685 106924 RMVar_ID_106924 Human_SNP_ID_184028774 m1A Human chr4 - 52659216 52659216 52659216 GCGCTGCCGCCCGGCCTCCCCGCCAGCGCGCCACCATGGGCAGTCCCGGTTTCCCCTTGTAAAGA GCGCTGCCGCCCGGCCTCCCCGCCAGCGCGCCGCCATGGGCAGTCCCGGTTTCCCCTTGTAAAGA T C USP46 Ensembl:ENSG00000109189 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:52659172..52659278 26863196 MeRIP-seq:(Medium) rs984618224 Functional Loss SNV dbSNP153 33..33 33 - - - 106925 RMVar_ID_106925 Human_SNP_ID_184028895 m1A Human chr4 + 52659488 52659488 52659488 GTTCCCGGGCCCCGCCGCGCCGCCTCCTTCCCAGCTCGCCCGCCCAGGCCTGGCCTCCTGCTTTT GTTCCCGGGCCCCGCCGCGCCGCCTCCTTCCCGGCTCGCCCGCCCAGGCCTGGCCTCCTGCTTTT A G USP46-AS1 Ensembl:ENSG00000248866 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:52659437..52659597 26863196 MeRIP-seq:(Medium) rs1400574085 Functional Loss SNV dbSNP153 33..33 33 - - - 106926 RMVar_ID_106926 Human_SNP_ID_184041071 m1A Human chr4 - 52712529 52712529 52712529 GAGACCGAAAGCCGAAGACTGGAGATGCACTCACCGCGCAACTCCAGCTGACAAAGAGGCCTGCG GAGACCGAAAGCCGAAGACTGGAGATGCACTCTCCGCGCAACTCCAGCTGACAAAGAGGCCTGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:52712476..52712579 26863196 MeRIP-seq:(Medium) rs1490486652 Functional Loss SNV dbSNP153 33..33 33 - - - 106927 RMVar_ID_106927 Human_SNP_ID_184202169 m1A Human chr4 + 53365775 53365775 53365775 CACCACCAATTGCGTCGGGCTCGAACTCTCGCAGGTGACAGTCAGGACCCCCCACCGCCTCCAGG CACCACCAATTGCGTCGGGCTCGAACTCTCGCCGGTGACAGTCAGGACCCCCCACCGCCTCCAGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:53365726..53365994 26863196 MeRIP-seq:(Medium) rs754168306 Functional Loss SNV dbSNP153 33..33 33 - - - 106928 RMVar_ID_106928 Human_SNP_ID_184205082 m1A Human chr4 - 53377791 53377791 53377791 AACTTAAACGCGGCGATCAACAGCCCCCTCCAACCCCTTCCCCAGCCTCGCAGCCCCGAGGCGCG AACTTAAACGCGGCGATCAACAGCCCCCTCCACCCCCTTCCCCAGCCTCGCAGCCCCGAGGCGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr4:53377663..53377925;chr4:53377692..53377842 26863196,32194978 MeRIP-seq:(Medium) rs906256878 Functional Loss SNV dbSNP153 33..33 33 - - - 106929 RMVar_ID_106929 Human_SNP_ID_184205156 m1A Human chr4 - 53377945 53377944 53377946 GCCAAGAGGGGAGGCCTGAGAGAACCCGAGAGACAGAGACAGGAAGTTTCGTACCGCCATAGAGC GCCAAGAGGGGAGGCCTGAGAGAACCCGAGA__CAGAGACAGGAAGTTTCGTACCGCCATAGAGC GTC G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:53377941..53378092 32194978 MeRIP-seq:(Medium) rs1192843724 Functional Loss DEL dbSNP153 32..33 33 - - - 106930 RMVar_ID_106930 Human_SNP_ID_184218353 m1A Human chr4 - 53427997 53427997 53427997 GACCTAAAATTAGAGCACAGTTAATTAAACAGATGCATAAATATTATGTAAGATTAATCTTAGTA GACCTAAAATTAGAGCACAGTTAATTAAACAGTTGCATAAATATTATGTAAGATTAATCTTAGTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:53427993..53428165 26863196 MeRIP-seq:(Medium) rs1467994399 Functional Loss SNV dbSNP153 33..33 33 - - - 106931 RMVar_ID_106931 Human_SNP_ID_184224056 m1A Human chr4 - 53453113 53453113 53453113 CACCCAACAAACCTGTTGAAAACACTTGGTGTAGGACTGTGATCACGCTCCCTCTCTCTCTCTCT CACCCAACAAACCTGTTGAAAACACTTGGTGTCGGACTGTGATCACGCTCCCTCTCTCTCTCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:53452976..53458555 26863196 MeRIP-seq:(Medium) rs1182490237 Functional Loss SNV dbSNP153 33..33 33 - - - 106932 RMVar_ID_106932 Human_SNP_ID_184224057 m1A Human chr4 + 53453114 53453114 53453114 GAGAGAGAGAGAGGGAGCGTGATCACAGTCCTACACCAAGTGTTTTCAACAGGTTTGTTGGGTGT GAGAGAGAGAGAGGGAGCGTGATCACAGTCCTGCACCAAGTGTTTTCAACAGGTTTGTTGGGTGT A G FIP1L1,AC058822.1 Ensembl:ENSG00000145216,Ensembl:ENSG00000282278 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:53442691..53458555 32194978 MeRIP-seq:(Medium) rs1382981546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71654,Human_RBP_ID_24058515,Human_RBP_ID_26349281 Human_Splice_Rec_561233,Human_Splice_Rec_561277,Human_Splice_Rec_561327,Human_Splice_Rec_561355,Human_Splice_Rec_561411,Human_Splice_Rec_561423,Human_Splice_Rec_561435 Human_miRNA_ID_1764021,Human_miRNA_ID_2478502,Human_miRNA_ID_2976508 RMVar_hsa_circ_66202,RMVar_hsa_circ_287073,RMVar_hsa_circ_58831,RMVar_hsa_circ_226046,RMVar_hsa_circ_331362,RMVar_hsa_circ_275829,RMVar_hsa_circ_226064,RMVar_hsa_circ_279321,RMVar_hsa_circ_119431,RMVar_hsa_circ_226068,RMVar_hsa_circ_226069,RMVar_hsa_circ_26566,RMVar_hsa_circ_33340,RMVar_hsa_circ_44197 106933 RMVar_ID_106933 Human_SNP_ID_184225206 m1A Human chr4 - 53458704 53458704 53458704 TGTCGTTCTTCTTTTTCTCGACTTGCTCTGTGACGCTCATAACCTCTTTCTGCATATTCCCTGTA TGTCGTTCTTCTTTTTCTCGACTTGCTCTGTGGCGCTCATAACCTCTTTCTGCATATTCCCTGTA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:53458624..53458834 26863196 MeRIP-seq:(Medium) rs1271823294 Functional Loss SNV dbSNP153 33..33 33 - - - 106934 RMVar_ID_106934 Human_SNP_ID_184699075 m1A Human chr4 - 55346346 55346346 55346346 CGGGTTCAGCGCCGAGTGCTCGGCCTCCGCCCAGGGAGCCATGGCCCGCGTGCCCGCCTTCCGCG CGGGTTCAGCGCCGAGTGCTCGGCCTCCGCCCGGGGAGCCATGGCCCGCGTGCCCGCCTTCCGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:55346295..55346447;chr4:55346300..55346384 26863196 MeRIP-seq:(Medium) rs1267289128 Functional Loss SNV dbSNP153 33..33 33 - - - 106935 RMVar_ID_106935 Human_SNP_ID_184711315 m1A Human chr4 + 55396183 55396174 55396183 CTCTTGCGGCGCCCGTGCGCGGCCGGCCCGGCAGGCGGGATGGCGGCCGCGGCTCCAGGGAACGG CTCTTGCGGCGCCCGTGCGCGGCC_________GGCGGGATGGCGGCCGCGGCTCCAGGGAACGG CGGCCCGGCA C TMEM165 Ensembl:ENSG00000134851 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:55395955..55396275 26863410 MeRIP-seq:(Medium) rs891651705 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_248986,Human_RBP_ID_4794608,Human_RBP_ID_9334693,Human_RBP_ID_18471859,Human_RBP_ID_22095511,Human_RBP_ID_22292087,Human_RBP_ID_22457870 RMVar_hsa_circ_81518,RMVar_hsa_circ_226108 106936 RMVar_ID_106936 Human_SNP_ID_184711320 m1A Human chr4 + 55396183 55396183 55396183 CTCTTGCGGCGCCCGTGCGCGGCCGGCCCGGCAGGCGGGATGGCGGCCGCGGCTCCAGGGAACGG CTCTTGCGGCGCCCGTGCGCGGCCGGCCCGGCGGGCGGGATGGCGGCCGCGGCTCCAGGGAACGG A G TMEM165 Ensembl:ENSG00000134851 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:55395955..55396275 26863410 MeRIP-seq:(Medium) rs1270697769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248986,Human_RBP_ID_4794608,Human_RBP_ID_9334693,Human_RBP_ID_18471859,Human_RBP_ID_22095511,Human_RBP_ID_22292087,Human_RBP_ID_22457870 RMVar_hsa_circ_81518,RMVar_hsa_circ_226108 106937 RMVar_ID_106937 Human_SNP_ID_184750344 m1A Human chr4 - 55546288 55546288 55546288 CCCTCTGGGGCAGCTGGGGTTACCTGCGGGGCAGGGGCGGGAGTGGGGTGCACGGCGGGGCCGGG CCCTCTGGGGCAGCTGGGGTTACCTGCGGGGCCGGGGCGGGAGTGGGGTGCACGGCGGGGCCGGG T G CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:55546237..55546355 26863196 MeRIP-seq:(Medium) rs1316420968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785961,Human_RBP_ID_837840,Human_RBP_ID_3747421,Human_RBP_ID_8130506,Human_RBP_ID_8211741,Human_RBP_ID_8236306,Human_RBP_ID_17156113,Human_RBP_ID_18500974,Human_RBP_ID_24384322,Human_RBP_ID_26791224 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 106938 RMVar_ID_106938 Human_SNP_ID_184750464 m1A Human chr4 + 55546520 55546520 55546520 GCTTGCGGCGGCTCCGGCTTCTTCCCTCCCCCACCCAGGTCTCCCGCTGCGGTGACTCGGAACCA GCTTGCGGCGGCTCCGGCTTCTTCCCTCCCCCCCCCAGGTCTCCCGCTGCGGTGACTCGGAACCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:55546514..55546615 26863196 MeRIP-seq:(Medium) rs1022095596 Functional Loss SNV dbSNP153 33..33 33 - - - 106939 RMVar_ID_106939 Human_SNP_ID_184750471 m1A Human chr4 - 55546535 55546535 55546535 ACACAGGCGGGGTAGTGGTTCCGAGTCACCGCAGCGGGAGACCTGGGTGGGGGAGGGAAGAAGCC ACACAGGCGGGGTAGTGGTTCCGAGTCACCGCTGCGGGAGACCTGGGTGGGGGAGGGAAGAAGCC T A CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:55546486..55546579 26863196 MeRIP-seq:(Medium) rs1280753067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4787236,Human_RBP_ID_8211744,Human_RBP_ID_9435802,Human_RBP_ID_18424758,Human_RBP_ID_18955223,Human_RBP_ID_22609964,Human_RBP_ID_25815471,Human_RBP_ID_26791606 Human_Splice_Rec_562525,Human_Splice_Rec_562553,Human_Splice_Rec_562559 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 106940 RMVar_ID_106940 Human_SNP_ID_184750472 m1A Human chr4 - 55546535 55546535 55546535 ACACAGGCGGGGTAGTGGTTCCGAGTCACCGCAGCGGGAGACCTGGGTGGGGGAGGGAAGAAGCC ACACAGGCGGGGTAGTGGTTCCGAGTCACCGCCGCGGGAGACCTGGGTGGGGGAGGGAAGAAGCC T G CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:55546486..55546579 26863196 MeRIP-seq:(Medium) rs1280753067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4787236,Human_RBP_ID_8211744,Human_RBP_ID_9435802,Human_RBP_ID_18424758,Human_RBP_ID_18955223,Human_RBP_ID_22609964,Human_RBP_ID_25815471,Human_RBP_ID_26791606 Human_Splice_Rec_562525,Human_Splice_Rec_562553,Human_Splice_Rec_562559 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 106941 RMVar_ID_106941 Human_SNP_ID_184771745 m1A Human chr4 - 55636177 55636177 55636177 CTCCCGCAGCCGCCGAGATGCTGCGAACAGAGAGCTGCCGCCCCAGGTCGCCCGCCGGACAGGTG CTCCCGCAGCCGCCGAGATGCTGCGAACAGAGGGCTGCCGCCCCAGGTCGCCCGCCGGACAGGTG T C NMU Ensembl:ENSG00000109255 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:55636142..55636254 26863196 MeRIP-seq:(Medium) rs1426084823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4794959,Human_RBP_ID_22533976 Human_Splice_Rec_562575,Human_Splice_Rec_562591,Human_Splice_Rec_562609,Human_Splice_Rec_562623 106942 RMVar_ID_106942 Human_SNP_ID_184845544 m1A Human chr4 + 55949036 55949015 55949036 TCGAGGCCTGAGGGCAATGCGGCTGGAGGCGGAGGCAACGGCGGCTGGAGCTGCCGGTGAGTCCG TCGAGGCCTGAG_____________________GGCAACGGCGGCTGGAGCTGCCGGTGAGTCCG GGGCAATGCGGCTGGAGGCGGA G CEP135 Ensembl:ENSG00000174799 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:55948987..55949107 26863196 MeRIP-seq:(Medium) rs1239792862 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_249600,Human_RBP_ID_8882140 Human_Splice_Rec_562829,Human_Splice_Rec_562839,Human_Splice_Rec_562841 106943 RMVar_ID_106943 Human_SNP_ID_184871735 m1A Human chr4 - 56060454 56060454 56060454 CCTCCATCTGTTACATTTCTACTCCTTCTCCAAGACCCAGCTCAGATATCACTTCCTCTGTGAGC CCTCCATCTGTTACATTTCTACTCCTTCTCCAGGACCCAGCTCAGATATCACTTCCTCTGTGAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:56060447..56060677 26863196 MeRIP-seq:(Medium) rs1433016899 Functional Loss SNV dbSNP153 33..33 33 - - - 106944 RMVar_ID_106944 Human_SNP_ID_184873317 m1A Human chr4 - 56068057 56068057 56068057 TTCCCCAACTCTGGGCCATGACCTGAAATATGACCTCTCTTATCCATTTGCTGCCTGCAGCCTCA TTCCCCAACTCTGGGCCATGACCTGAAATATGTCCTCTCTTATCCATTTGCTGCCTGCAGCCTCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56068050..56068211 26863196 MeRIP-seq:(Medium) rs1475208411 Functional Loss SNV dbSNP153 33..33 33 - - - 106945 RMVar_ID_106945 Human_SNP_ID_184873504 m1A Human chr4 - 56068980 56068980 56068980 ATGTCTCCGTGTCCTCTTCTCCTTTCACAGGGACACTAGTCACTGGATTTAGGGCTCACTATAAA ATGTCTCCGTGTCCTCTTCTCCTTTCACAGGGGCACTAGTCACTGGATTTAGGGCTCACTATAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56068974..56069091 26863196 MeRIP-seq:(Medium) rs1300956565 Functional Loss SNV dbSNP153 33..33 33 - - - 106946 RMVar_ID_106946 Human_SNP_ID_184898893 m1A Human chr4 - 56181327 56181327 56181327 TGACTGGCTCCTGGCTGTGGCTGGAACACCCCAGCTGCATTCCCTCCTTAGGGCCTTTACACCCA TGACTGGCTCCTGGCTGTGGCTGGAACACCCCTGCTGCATTCCCTCCTTAGGGCCTTTACACCCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:56181246..56181330 26863196 MeRIP-seq:(Medium) rs1304122244 Functional Loss SNV dbSNP153 33..33 33 - - - 106947 RMVar_ID_106947 Human_SNP_ID_184901953 m1A Human chr4 + 56193365 56193365 56193365 CCAAACCATGTCACCAGCCTCGGGATACACCCACCACATAAAATGATCAAAGTTTGTTATCATAG CCAAACCATGTCACCAGCCTCGGGATACACCCGCCACATAAAATGATCAAAGTTTGTTATCATAG A G CRACD Ensembl:ENSG00000109265 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:56193238..56193413 26863196 MeRIP-seq:(Medium) rs1162428718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348885,RMVar_hsa_circ_342658,RMVar_hsa_circ_226209 106948 RMVar_ID_106948 Human_SNP_ID_184930366 m1A Human chr4 + 56314527 56314527 56314527 GAGGCGGCGGCTGGAGGAGGACGCCAGGCTGGAGGAGCGGAGGCGGCAGGAGGAGGAGGAAGGAA GAGGCGGCGGCTGGAGGAGGACGCCAGGCTGGGGGAGCGGAGGCGGCAGGAGGAGGAGGAAGGAA A G CRACD Ensembl:ENSG00000109265 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:56314399..56314820 26863196 MeRIP-seq:(Medium) rs1305564060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302627,RMVar_hsa_circ_266430,RMVar_hsa_circ_30363,RMVar_hsa_circ_226214 106949 RMVar_ID_106949 Human_SNP_ID_184931052 m1A Human chr4 - 56315808 56315808 56315808 GGTGCATCTCCGACTTCTCCGGACCCTTCCCGAGCTCGCGAACACCAGCAGGAGGAGGCTGGGGG GGTGCATCTCCGACTTCTCCGGACCCTTCCCGTGCTCGCGAACACCAGCAGGAGGAGGCTGGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:56315758..56315849 26863196 MeRIP-seq:(Medium) rs368136106 Functional Loss SNV dbSNP153 33..33 33 - - - 106950 RMVar_ID_106950 Human_SNP_ID_184931169 m1A Human chr4 + 56316101 56316098 56316101 TGCGCTTCAACTGCGACCAACAGGCAGAACAGAAGAAGAAGAAGAGGCACAGCAGCACCGGAGAC TGCGCTTCAACTGCGACCAACAGGCAGAAC___AGAAGAAGAAGAGGCACAGCAGCACCGGAGAC CAGA C CRACD Ensembl:ENSG00000109265 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56316050..56316484 26863196 MeRIP-seq:(Medium) rs748490494 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_302627,RMVar_hsa_circ_266430,RMVar_hsa_circ_30363,RMVar_hsa_circ_226214,RMVar_hsa_circ_226215 106951 RMVar_ID_106951 Human_SNP_ID_184960924 m1A Human chr4 - 56435473 56435473 56435473 GGTCCTTCCACGTGCTTTCGGCGGCGACATGGAGCTGGAGGAGTTGGGGATCCGAGAGGAATGTG GGTCCTTCCACGTGCTTTCGGCGGCGACATGGGGCTGGAGGAGTTGGGGATCCGAGAGGAATGTG T C PPAT Ensembl:ENSG00000128059 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:56435395..56435590 26863196 MeRIP-seq:(Medium) rs573844517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249394,Human_RBP_ID_787059,Human_RBP_ID_4794967,Human_RBP_ID_5475608,Human_RBP_ID_7350967,Human_RBP_ID_8943687,Human_RBP_ID_9304159,Human_RBP_ID_9335014,Human_RBP_ID_19013734,Human_RBP_ID_22096263,Human_RBP_ID_23034801,Human_RBP_ID_26349295 106952 RMVar_ID_106952 Human_SNP_ID_184961332 m1A Human chr4 + 56436319 56436319 56436319 TCGCAGCCCTCAGCCCACTTAGGATAATGGCGACAGCTGAGGGTGAGTAACAGGGATCCGGGCCC TCGCAGCCCTCAGCCCACTTAGGATAATGGCGGCAGCTGAGGGTGAGTAACAGGGATCCGGGCCC A G PAICS Ensembl:ENSG00000128050 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:56436183..56441791;chr4:56436197..56436378;chr4:56436201..56441686;chr4:56436251..56436350 31548705,26863196 m1A-IP-seq:(High) rs1044061502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1317379,Human_RBP_ID_4794611,Human_RBP_ID_9334705,Human_RBP_ID_18032333,Human_RBP_ID_19122542 Human_Splice_Rec_563292,Human_Splice_Rec_563293,Human_Splice_Rec_563310,Human_Splice_Rec_563311,Human_Splice_Rec_563328,Human_Splice_Rec_563329,Human_Splice_Rec_563345,Human_Splice_Rec_563347,Human_Splice_Rec_563349,Human_Splice_Rec_563367 106953 RMVar_ID_106953 Human_SNP_ID_184962843 m1A Human chr4 + 56441736 56441736 56441736 GAAGTCTACGAATTGTTAGACAGTCCAGGAAAAGTCCTCCTGCAGTCCAAGGACCAGATTACAGC GAAGTCTACGAATTGTTAGACAGTCCAGGAAAGGTCCTCCTGCAGTCCAAGGACCAGATTACAGC A G PAICS Ensembl:ENSG00000128050 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:56441685..56441835 32194978 MeRIP-seq:(Medium) rs1473456327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72602,Human_RBP_ID_622452,Human_RBP_ID_1639481,Human_RBP_ID_1979879,Human_RBP_ID_3741687,Human_RBP_ID_7319536,Human_RBP_ID_8593334,Human_RBP_ID_9161510,Human_RBP_ID_15178461,Human_RBP_ID_18825343,Human_RBP_ID_22458596,Human_RBP_ID_24059619,Human_RBP_ID_27068777 Human_Splice_Rec_563294,Human_Splice_Rec_563312,Human_Splice_Rec_563330,Human_Splice_Rec_563346,Human_Splice_Rec_563348,Human_Splice_Rec_563350,Human_Splice_Rec_563368 RMVar_hsa_circ_55288,RMVar_hsa_circ_336530 106954 RMVar_ID_106954 Human_SNP_ID_184963911 m1A Human chr4 + 56446781 56446781 56446781 AGTGTGAAATGATTCCAATTGAATGGGTTTGCAGAAGAATAGCAACTGGTTCTTTTCTCAAAAGA AGTGTGAAATGATTCCAATTGAATGGGTTTGCGGAAGAATAGCAACTGGTTCTTTTCTCAAAAGA A G PAICS Ensembl:ENSG00000128050 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1312223382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24059624 Human_Splice_Rec_563296,Human_Splice_Rec_563297,Human_Splice_Rec_563314,Human_Splice_Rec_563315,Human_Splice_Rec_563332,Human_Splice_Rec_563333,Human_Splice_Rec_563354,Human_Splice_Rec_563355,Human_Splice_Rec_563370,Human_Splice_Rec_563371 RMVar_hsa_circ_55288,RMVar_hsa_circ_336530 106955 RMVar_ID_106955 Human_SNP_ID_184965242 m1A Human chr4 - 56452054 56452050 56452054 AATACCTGAAATGTCCATATTACTTGTGGTTTACCTTCATACTCAGCTTTAATCCTCAGAGTTTC AATACCTGAAATGTCCATATTACTTGTGGTTT____TCATACTCAGCTTTAATCCTCAGAGTTTC AAGGT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:56452042..56453743 32194978 MeRIP-seq:(Medium) rs1429929350 Functional Loss DEL dbSNP153 33..36 33 - - - 106956 RMVar_ID_106956 Human_SNP_ID_184967148 m1A Human chr4 + 56459912 56459912 56459912 TCTCCAGACTTGCATTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTGTCGCCCAGGCTGGAGTG TCTCCAGACTTGCATTTTTTTTTTTTTTTTTGTGACAGGGTCTCACTGTCGCCCAGGCTGGAGTG A T PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1465765991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4799945,Human_RBP_ID_7319650,Human_RBP_ID_26518376 Human_miRNA_ID_1102636,Human_miRNA_ID_1529844,Human_miRNA_ID_1950231,Human_miRNA_ID_1951515,Human_miRNA_ID_2443610 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 106957 RMVar_ID_106957 Human_SNP_ID_184967212 m1A Human chr4 + 56460147 56460147 56460147 GAACCCTAGTAATTCTCCTATCTCAGCCTCCCAAAGTGCTAGGGTTACAGACATGAGCCACTGTG GAACCCTAGTAATTCTCCTATCTCAGCCTCCCGAAGTGCTAGGGTTACAGACATGAGCCACTGTG A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1409470477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622495,Human_RBP_ID_8265833,Human_RBP_ID_17575131,Human_RBP_ID_22458608,Human_RBP_ID_23191127,Human_RBP_ID_26516100,Human_RBP_ID_27508715 Human_miRNA_ID_2978639 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 106958 RMVar_ID_106958 Human_SNP_ID_184967679 m1A Human chr4 + 56462165 56462165 56462165 CAAAATGAGGACGGTGATGGGGATAAGAGGGGAAGGTTTTTGAGGAGAGCAGAGCAATGATGTAA CAAAATGAGGACGGTGATGGGGATAAGAGGGGTAGGTTTTTGAGGAGAGCAGAGCAATGATGTAA A T PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56462115..56462210 26863196 MeRIP-seq:(Medium) rs1037069527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7319712 106959 RMVar_ID_106959 Human_SNP_ID_184968999 m1A Human chr4 + 56467353 56467353 56467353 GGACGCTGCCTCGACCATGGCGGTCTCCTGGAAACAGGCTGCTTTGAGCCGAAACTGGTGACCGT GGACGCTGCCTCGACCATGGCGGTCTCCTGGACACAGGCTGCTTTGAGCCGAAACTGGTGACCGT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:56467302..56467402 32194978 MeRIP-seq:(Medium) rs990663858 Functional Loss SNV dbSNP153 33..33 33 - - - 106960 RMVar_ID_106960 Human_SNP_ID_184969038 m1A Human chr4 - 56467493 56467493 56467493 GTGTCTTCAGCCCTAAGGCAGCATCAGAGATCATAATCTTCTGCTCTCGTGGCAAGAAATTTGTG GTGTCTTCAGCCCTAAGGCAGCATCAGAGATCGTAATCTTCTGCTCTCGTGGCAAGAAATTTGTG T C lnc-PPAT-1,lnc-PPAT-1:2 RNACentral:URS00009B260E,RNACentral:URS00008C04B3 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:56467444..56467528 26863196 MeRIP-seq:(Medium) rs1426440489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8128622,Human_RBP_ID_22292269 106961 RMVar_ID_106961 Human_SNP_ID_184969051 m1A Human chr4 - 56467517 56467517 56467517 TTGCTAAGCGTCGCCGAGTTGGGAGTGTCTTCAGCCCTAAGGCAGCATCAGAGATCATAATCTTC TTGCTAAGCGTCGCCGAGTTGGGAGTGTCTTCGGCCCTAAGGCAGCATCAGAGATCATAATCTTC T C lnc-PPAT-1,lnc-PPAT-1:2 RNACentral:URS00009B260E,RNACentral:URS00008C04B3 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:56467432..56467535 26863196 MeRIP-seq:(Medium) rs1021130064 Functional Loss SNV dbSNP153 33..33 33 - - - 106962 RMVar_ID_106962 Human_SNP_ID_184969160 m1A Human chr4 - 56467676 56467676 56467676 CGTTCTGGCCATACCGGTTCACTTCACTCCACAGCGCAGGTACTGACACCCCCCCGCTGCCGCCG CGTTCTGGCCATACCGGTTCACTTCACTCCACGGCGCAGGTACTGACACCCCCCCGCTGCCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:56467626..56467750 26863196 MeRIP-seq:(Medium) rs1303603626 Functional Loss SNV dbSNP153 33..33 33 - - - 106963 RMVar_ID_106963 Human_SNP_ID_185080771 m1A Human chr4 + 56908020 56908020 56908020 CCCAGACCCTGGCGGCGGCTGCCGCAGCCGAGACGGCAGGGCGAGGCCCGGAGGCCTGAGCACCC CCCAGACCCTGGCGGCGGCTGCCGCAGCCGAGGCGGCAGGGCGAGGCCCGGAGGCCTGAGCACCC A G REST Ensembl:ENSG00000084093 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56907972..56908089 26863196 MeRIP-seq:(Medium) rs1199472402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4787789 106964 RMVar_ID_106964 Human_SNP_ID_185087450 m1A Human chr4 - 56930922 56930922 56930922 GCAACCTCCGTCTGAGCAGTCTCCATGGGAGGAGGCAGCTCCATGTGAGCAAGTACAATTTGGGC GCAACCTCCGTCTGAGCAGTCTCCATGGGAGGGGGCAGCTCCATGTGAGCAAGTACAATTTGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:56930528..56930928 32194978 MeRIP-seq:(Medium) rs922596945 Functional Loss SNV dbSNP153 33..33 33 - - - 106965 RMVar_ID_106965 Human_SNP_ID_185087451 m1A Human chr4 - 56930922 56930922 56930922 GCAACCTCCGTCTGAGCAGTCTCCATGGGAGGAGGCAGCTCCATGTGAGCAAGTACAATTTGGGC GCAACCTCCGTCTGAGCAGTCTCCATGGGAGGCGGCAGCTCCATGTGAGCAAGTACAATTTGGGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:56930528..56930928 32194978 MeRIP-seq:(Medium) rs922596945 Functional Loss SNV dbSNP153 33..33 33 - - - 106966 RMVar_ID_106966 Human_SNP_ID_185087566 m1A Human chr4 + 56931128 56931128 56931128 GATAGAGCTGTCTCCTCCCATGGAGGTGGTCCAGAAGGAACCTGTTAAGATAGAGCTGTCTCCTC GATAGAGCTGTCTCCTCCCATGGAGGTGGTCCGGAAGGAACCTGTTAAGATAGAGCTGTCTCCTC A G REST Ensembl:ENSG00000084093 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:56931077..56931178 32194978 MeRIP-seq:(Medium) rs1325154191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27824809 106967 RMVar_ID_106967 Human_SNP_ID_185100309 m1A Human chr4 - 56977317 56977316 56977317 GGATCCGGAGCCGCAACCCACCCGCGAAAAGCAGCTGCAGGAGCTCCAGCAACAGCAGGAGGAGG GGATCCGGAGCCGCAACCCACCCGCGAAAAGC_GCTGCAGGAGCTCCAGCAACAGCAGGAGGAGG CT C NOA1 Ensembl:ENSG00000084092 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:56977268..56977383 26863196 MeRIP-seq:(Medium) rs1560466668 Functional Loss DEL dbSNP153 33..33 33 - - - 106968 RMVar_ID_106968 Human_SNP_ID_185100316 m1A Human chr4 - 56977330 56977330 56977330 CGGAGTACATCCTGGATCCGGAGCCGCAACCCACCCGCGAAAAGCAGCTGCAGGAGCTCCAGCAA CGGAGTACATCCTGGATCCGGAGCCGCAACCCTCCCGCGAAAAGCAGCTGCAGGAGCTCCAGCAA T A NOA1 Ensembl:ENSG00000084092 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56977282..56977349 26863196 MeRIP-seq:(Medium) rs3733307 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9335017,Human_RBP_ID_22095530,Human_RBP_ID_22457689,Human_RBP_ID_27508793 106969 RMVar_ID_106969 Human_SNP_ID_185100317 m1A Human chr4 - 56977330 56977330 56977330 CGGAGTACATCCTGGATCCGGAGCCGCAACCCACCCGCGAAAAGCAGCTGCAGGAGCTCCAGCAA CGGAGTACATCCTGGATCCGGAGCCGCAACCCGCCCGCGAAAAGCAGCTGCAGGAGCTCCAGCAA T C NOA1 Ensembl:ENSG00000084092 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56977282..56977349 26863196 MeRIP-seq:(Medium) rs3733307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9335017,Human_RBP_ID_22095530,Human_RBP_ID_22457689,Human_RBP_ID_27508793 106970 RMVar_ID_106970 Human_SNP_ID_185113956 m1A Human chr4 + 57033250 57033250 57033250 GCTTTTCTGGGCCACCCCGGGTCTGAATGGCCAGGTTGTCCCGGTCACCAGGCAGGAGTTCTGTC GCTTTTCTGGGCCACCCCGGGTCTGAATGGCCGGGTTGTCCCGGTCACCAGGCAGGAGTTCTGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:57033154..57033355 26863196 MeRIP-seq:(Medium) rs1462113745 Functional Loss SNV dbSNP153 33..33 33 - - - 106971 RMVar_ID_106971 Human_SNP_ID_185132345 m1A Human chr4 + 57110335 57110335 57110335 GCAGCCCAGCGGCGCCGAGGAGCAGGGCGCGCAGCGACGGCCGCTCCATGGCGGGGTGCGGTGGC GCAGCCCAGCGGCGCCGAGGAGCAGGGCGCGCGGCGACGGCCGCTCCATGGCGGGGTGCGGTGGC A G IGFBP7-AS1 Ensembl:ENSG00000245067 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr4:57065567..57110400;chr4:57110201..57110400;chr4:57109926..57110400;chr4:57110056..57110375 26863196 MeRIP-seq:(Medium) rs776088536 Functional Loss SNV dbSNP153 33..33 33 - - - 106972 RMVar_ID_106972 Human_SNP_ID_413896017 m1A Human chr9 - 120392583 120392583 120392583 TGGGGAGCAATGCTCTGCATAGGTCTAGAGAAAGGCAGAACTCTCTGCATTGGCATCTCTCCTCC TGGGGAGCAATGCTCTGCATAGGTCTAGAGAAGGGCAGAACTCTCTGCATTGGCATCTCTCCTCC T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120392577..120392808 26863196 MeRIP-seq:(Medium) rs1280399844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116831,RMVar_hsa_circ_118485,RMVar_hsa_circ_259086,RMVar_hsa_circ_259087 106973 RMVar_ID_106973 Human_SNP_ID_413900008 m1A Human chr9 - 120409188 120409185 120409188 AAAATGAAAGGCTGCAGAAAGAAGGCAGCGAGAAGGAGAGACACAACCAGCAGCTGATCCAGGAG AAAATGAAAGGCTGCAGAAAGAAGGCAGCGAG___GAGAGACACAACCAGCAGCTGATCCAGGAG CCTT C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:120409098..120409237 26863196 MeRIP-seq:(Medium) rs765852426 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_963665,Human_RBP_ID_5535032,Human_RBP_ID_9315625,Human_RBP_ID_9407284,Human_RBP_ID_19024254,Human_RBP_ID_27832619 Human_Splice_Rec_1075535,Human_Splice_Rec_1075607,Human_Splice_Rec_1075679,Human_Splice_Rec_1075759,Human_Splice_Rec_1075831,Human_Splice_Rec_1075875,Human_Splice_Rec_1075933,Human_Splice_Rec_1075993 RMVar_hsa_circ_10077,RMVar_hsa_circ_116831,RMVar_hsa_circ_118485,RMVar_hsa_circ_259086,RMVar_hsa_circ_259087,RMVar_hsa_circ_54240,RMVar_hsa_circ_68537,RMVar_hsa_circ_339467,RMVar_hsa_circ_113910,RMVar_hsa_circ_259088,RMVar_hsa_circ_69233,RMVar_hsa_circ_335637,RMVar_hsa_circ_357477,RMVar_hsa_circ_365094,RMVar_hsa_circ_69357,RMVar_hsa_circ_61630,RMVar_hsa_circ_65467,RMVar_hsa_circ_259089 106974 RMVar_ID_106974 Human_SNP_ID_413900016 m1A Human chr9 - 120409214 120409214 120409214 GCGGGAGTATGCCAGCGTGAAGGAAGAAAATGAAAGGCTGCAGAAAGAAGGCAGCGAGAAGGAGA GCGGGAGTATGCCAGCGTGAAGGAAGAAAATGGAAGGCTGCAGAAAGAAGGCAGCGAGAAGGAGA T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120409126..120409275 26863196 MeRIP-seq:(Medium) rs542203722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19024254,Human_RBP_ID_26361981 Human_Splice_Rec_1075535,Human_Splice_Rec_1075607,Human_Splice_Rec_1075679,Human_Splice_Rec_1075759,Human_Splice_Rec_1075831,Human_Splice_Rec_1075875,Human_Splice_Rec_1075933,Human_Splice_Rec_1075993 RMVar_hsa_circ_10077,RMVar_hsa_circ_116831,RMVar_hsa_circ_118485,RMVar_hsa_circ_259086,RMVar_hsa_circ_259087,RMVar_hsa_circ_54240,RMVar_hsa_circ_68537,RMVar_hsa_circ_339467,RMVar_hsa_circ_113910,RMVar_hsa_circ_259088,RMVar_hsa_circ_69233,RMVar_hsa_circ_335637,RMVar_hsa_circ_357477,RMVar_hsa_circ_365094,RMVar_hsa_circ_69357,RMVar_hsa_circ_61630,RMVar_hsa_circ_65467,RMVar_hsa_circ_259089 106975 RMVar_ID_106975 Human_SNP_ID_413900018 m1A Human chr9 - 120409218 120409218 120409218 TTCAGCGGGAGTATGCCAGCGTGAAGGAAGAAAATGAAAGGCTGCAGAAAGAAGGCAGCGAGAAG TTCAGCGGGAGTATGCCAGCGTGAAGGAAGAAGATGAAAGGCTGCAGAAAGAAGGCAGCGAGAAG T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120409098..120409275 26863196 MeRIP-seq:(Medium) rs1389402765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19024254,Human_RBP_ID_26361981 Human_Splice_Rec_1075534,Human_Splice_Rec_1075535,Human_Splice_Rec_1075606,Human_Splice_Rec_1075607,Human_Splice_Rec_1075678,Human_Splice_Rec_1075679,Human_Splice_Rec_1075758,Human_Splice_Rec_1075759,Human_Splice_Rec_1075830,Human_Splice_Rec_1075831,Human_Splice_Rec_1075874,Human_Splice_Rec_1075875,Human_Splice_Rec_1075932,Human_Splice_Rec_1075933,Human_Splice_Rec_1075992,Human_Splice_Rec_1075993 RMVar_hsa_circ_10077,RMVar_hsa_circ_116831,RMVar_hsa_circ_118485,RMVar_hsa_circ_259086,RMVar_hsa_circ_259087,RMVar_hsa_circ_54240,RMVar_hsa_circ_68537,RMVar_hsa_circ_339467,RMVar_hsa_circ_113910,RMVar_hsa_circ_259088,RMVar_hsa_circ_69233,RMVar_hsa_circ_335637,RMVar_hsa_circ_357477,RMVar_hsa_circ_365094,RMVar_hsa_circ_69357,RMVar_hsa_circ_61630,RMVar_hsa_circ_65467,RMVar_hsa_circ_259089 106976 RMVar_ID_106976 Human_SNP_ID_413901953 m1A Human chr9 + 120417167 120417164 120417167 AACTGCTGGCGCCCACGGCACTGCACCTCCCCACGCCTTAAACTGCTGGCGCCCACGGCACTGCA AACTGCTGGCGCCCACGGCACTGCACCTCC___CGCCTTAAACTGCTGGCGCCCACGGCACTGCA CCCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120417164..120417317 26863196 MeRIP-seq:(Medium) rs1473979892 Functional Loss DEL dbSNP153 31..33 33 - - - 106977 RMVar_ID_106977 Human_SNP_ID_413901956 m1A Human chr9 + 120417167 120417167 120417167 AACTGCTGGCGCCCACGGCACTGCACCTCCCCACGCCTTAAACTGCTGGCGCCCACGGCACTGCA AACTGCTGGCGCCCACGGCACTGCACCTCCCCGCGCCTTAAACTGCTGGCGCCCACGGCACTGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120417164..120417317 26863196 MeRIP-seq:(Medium) rs1026683379 Functional Loss SNV dbSNP153 33..33 33 - - - 106978 RMVar_ID_106978 Human_SNP_ID_413909374 m1A Human chr9 + 120448787 120448787 120448787 GATTTTTAAGTTTCCCTTTATTCTTGCCACCCACTTTCACTACTCATCAGGGTCCATTAATTATA GATTTTTAAGTTTCCCTTTATTCTTGCCACCCGCTTTCACTACTCATCAGGGTCCATTAATTATA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120448785..120449035 26863196 MeRIP-seq:(Medium) rs1423828302 Functional Loss SNV dbSNP153 33..33 33 - - - 106979 RMVar_ID_106979 Human_SNP_ID_413930143 m1A Human chr9 + 120536353 120536353 120536353 CACGCTGCCAGATAATGTGATGTCAGGGTATGACAGGGACAAGAGCCAGACCTGTCTTTCTCATC CACGCTGCCAGATAATGTGATGTCAGGGTATGTCAGGGACAAGAGCCAGACCTGTCTTTCTCATC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:120536351..120536475 26863196 MeRIP-seq:(Medium) rs772090088 Functional Loss SNV dbSNP153 33..33 33 - - - 106980 RMVar_ID_106980 Human_SNP_ID_413930172 m1A Human chr9 - 120536427 120536427 120536427 GGTTGCGTTTGGAAAGCAAGCTTTCAGAGATGAAGAAGATGCACGAGGGGGACTTGGCGATGGCT GGTTGCGTTTGGAAAGCAAGCTTTCAGAGATGGAGAAGATGCACGAGGGGGACTTGGCGATGGCT T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120536311..120536465 26863196 MeRIP-seq:(Medium) rs1414467945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963676,Human_RBP_ID_9407317,Human_RBP_ID_16551907,Human_RBP_ID_18472767,Human_RBP_ID_19025503,Human_RBP_ID_22748023,Human_RBP_ID_23094823,Human_RBP_ID_26362009,Human_RBP_ID_27833336 Human_Splice_Rec_1075495,Human_Splice_Rec_1075561,Human_Splice_Rec_1075633,Human_Splice_Rec_1075711,Human_Splice_Rec_1075785,Human_Splice_Rec_1075949,Human_Splice_Rec_1076013,Human_Splice_Rec_1076027 Human_miRNA_ID_2794344,Human_miRNA_ID_2794810,Human_miRNA_ID_2795277 RMVar_hsa_circ_4108,RMVar_hsa_circ_1987,RMVar_hsa_circ_10527,RMVar_hsa_circ_48901,RMVar_hsa_circ_2455,RMVar_hsa_circ_18907,RMVar_hsa_circ_56473,RMVar_hsa_circ_61186,RMVar_hsa_circ_16854,RMVar_hsa_circ_364131,RMVar_hsa_circ_58098,RMVar_hsa_circ_362671,RMVar_hsa_circ_367036,RMVar_hsa_circ_355424,RMVar_hsa_circ_74482,RMVar_hsa_circ_64001,RMVar_hsa_circ_50901,RMVar_hsa_circ_60736,RMVar_hsa_circ_305970,RMVar_hsa_circ_259102,RMVar_hsa_circ_347562,RMVar_hsa_circ_71658,RMVar_hsa_circ_60200,RMVar_hsa_circ_354900,RMVar_hsa_circ_356464,RMVar_hsa_circ_362128,RMVar_hsa_circ_351040,RMVar_hsa_circ_286301,RMVar_hsa_circ_73595,RMVar_hsa_circ_352245,RMVar_hsa_circ_259108,RMVar_hsa_circ_360298,RMVar_hsa_circ_62508,RMVar_hsa_circ_356481,RMVar_hsa_circ_360978,RMVar_hsa_circ_320799,RMVar_hsa_circ_358333,RMVar_hsa_circ_329059,RMVar_hsa_circ_38496,RMVar_hsa_circ_59752,RMVar_hsa_circ_259109,RMVar_hsa_circ_317762 106981 RMVar_ID_106981 Human_SNP_ID_413937277 m1A Human chr9 - 120565322 120565322 120565322 GAGTTAAAAGGCTGCTGTGGTGTTGTGGGCCCAAAGGGAGGAATGTGGAGCTAAGGGCATGGAAT GAGTTAAAAGGCTGCTGTGGTGTTGTGGGCCCCAAGGGAGGAATGTGGAGCTAAGGGCATGGAAT T G CDK5RAP2 Ensembl:ENSG00000136861 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:120565296..120565403 26863196 MeRIP-seq:(Medium) rs954317614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16552421 RMVar_hsa_circ_48901,RMVar_hsa_circ_2455,RMVar_hsa_circ_18907,RMVar_hsa_circ_56473,RMVar_hsa_circ_16854,RMVar_hsa_circ_362671,RMVar_hsa_circ_355424,RMVar_hsa_circ_50901,RMVar_hsa_circ_305970,RMVar_hsa_circ_71658,RMVar_hsa_circ_354900,RMVar_hsa_circ_362128,RMVar_hsa_circ_360298,RMVar_hsa_circ_360978,RMVar_hsa_circ_320799,RMVar_hsa_circ_259110,RMVar_hsa_circ_59752,RMVar_hsa_circ_259109,RMVar_hsa_circ_312795,RMVar_hsa_circ_317762,RMVar_hsa_circ_359140,RMVar_hsa_circ_278350,RMVar_hsa_circ_259111,RMVar_hsa_circ_301210 106982 RMVar_ID_106982 Human_SNP_ID_413940840 m1A Human chr9 - 120580011 120580011 120580011 CTATCGCGGGGGGTACTAGTGGCGCCGCCGCCACAGACACCAACGCTGTCGCCACCTCTGTAGCC CTATCGCGGGGGGTACTAGTGGCGCCGCCGCCGCAGACACCAACGCTGTCGCCACCTCTGTAGCC T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:120579966..120580124 26863196 MeRIP-seq:(Medium) rs1564400773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1118066,Human_RBP_ID_3974733,Human_RBP_ID_5154441,Human_RBP_ID_9441992,Human_RBP_ID_18427201,Human_RBP_ID_18962241,Human_RBP_ID_22628179,Human_RBP_ID_23094655,Human_RBP_ID_26361013,Human_RBP_ID_27832649,Human_RBP_ID_27843616 Human_Splice_Rec_1075485,Human_Splice_Rec_1075551,Human_Splice_Rec_1075623,Human_Splice_Rec_1075701,Human_Splice_Rec_1075775,Human_Splice_Rec_1076017,Human_Splice_Rec_1076035 106983 RMVar_ID_106983 Human_SNP_ID_413940852 m1A Human chr9 + 120580030 120580030 120580030 GCGTTGGTGTCTGTGGCGGCGGCGCCACTAGTACCCCCCGCGATAGCGACCCGCCGGGCTCCCCA GCGTTGGTGTCTGTGGCGGCGGCGCCACTAGTCCCCCCCGCGATAGCGACCCGCCGGGCTCCCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120579983..120580102 26863196 MeRIP-seq:(Medium) rs1036373453 Functional Loss SNV dbSNP153 33..33 33 - - - 106984 RMVar_ID_106984 Human_SNP_ID_413971962 m1A Human chr9 - 120713867 120713867 120713867 CCGGCGCCGACCACCCCTGTAGCGACCACCGTACCGGCGCCCACGACTCCCCGGACCCCGACCCC CCGGCGCCGACCACCCCTGTAGCGACCACCGTGCCGGCGCCCACGACTCCCCGGACCCCGACCCC T C MEGF9 Ensembl:ENSG00000106780 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120713816..120714013 26863196 MeRIP-seq:(Medium) rs746513265 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_256528,Human_RBP_ID_5007706 106985 RMVar_ID_106985 Human_SNP_ID_413971963 m1A Human chr9 - 120713867 120713867 120713867 CCGGCGCCGACCACCCCTGTAGCGACCACCGTACCGGCGCCCACGACTCCCCGGACCCCGACCCC CCGGCGCCGACCACCCCTGTAGCGACCACCGTCCCGGCGCCCACGACTCCCCGGACCCCGACCCC T G MEGF9 Ensembl:ENSG00000106780 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120713816..120714013 26863196 MeRIP-seq:(Medium) rs746513265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256528,Human_RBP_ID_5007706 106986 RMVar_ID_106986 Human_SNP_ID_413972031 m1A Human chr9 + 120714022 120714022 120714022 CGAGGGGCCGAGCGGCGCCTGAAAGGTGGTGGAAGAGGGTCCAGCAGTCGCCCAAAGAGGGGTGG CGAGGGGCCGAGCGGCGCCTGAAAGGTGGTGGCAGAGGGTCCAGCAGTCGCCCAAAGAGGGGTGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:120713973..120714161 26863196 MeRIP-seq:(Medium) rs201403181 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 106987 RMVar_ID_106987 Human_SNP_ID_413972171 m1A Human chr9 - 120714354 120714351 120714355 ATGACTGACCAACCGACTGGCTGAATGAATGAATGGCGGAGCCGAGCGCGCCATGAGGAGCCTGC ATGACTGACCAACCGACTGGCTGAATGAATG____GCGGAGCCGAGCGCGCCATGAGGAGCCTGC CCATT C MEGF9 Ensembl:ENSG00000106780 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:120714247..120714400 26863196 MeRIP-seq:(Medium) rs1382190641 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5037021,Human_RBP_ID_8239231,Human_RBP_ID_8695246,Human_RBP_ID_22118829,Human_RBP_ID_24281941 106988 RMVar_ID_106988 Human_SNP_ID_413972197 m1A Human chr9 + 120714425 120714425 120714425 CTCGTTGCAATCCGACCAAGGAAGCCTCCGCAACCGCCGCCGCCACCGCCACCGGGCGCACCATC CTCGTTGCAATCCGACCAAGGAAGCCTCCGCAGCCGCCGCCGCCACCGCCACCGGGCGCACCATC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120714064..120714475 26863196 MeRIP-seq:(Medium) rs1352072707 Functional Loss SNV dbSNP153 33..33 33 - - - 106989 RMVar_ID_106989 Human_SNP_ID_413991217 m1A Human chr9 - 120793361 120793361 120793361 CTGTGAGGCTGCGGACCGGGAGCAGCGGCCGCAGGTCCGGGTCTGTATGCGAGGCGGGGCCGGTC CTGTGAGGCTGCGGACCGGGAGCAGCGGCCGCGGGTCCGGGTCTGTATGCGAGGCGGGGCCGGTC T C FBXW2 Ensembl:ENSG00000119402 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:120793077..120793400 26863196 MeRIP-seq:(Medium) rs945342106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036353,Human_RBP_ID_18427787,Human_RBP_ID_19143775,Human_RBP_ID_23094481 Human_Splice_Rec_1076053,Human_Splice_Rec_1076067,Human_Splice_Rec_1076085 RMVar_hsa_circ_117191,RMVar_hsa_circ_259120 106990 RMVar_ID_106990 Human_SNP_ID_414002923 m1A Human chr9 - 120842803 120842786 120842803 TCACTCCGTGCTGCAGGCAGTGCCGCTCAACGAGCTTCGCCAGCAAGCGGCGGAGCTGCGCCTCG TCACTCCGTGCTGCAGGCAGTGCCGCTCAACG_________________GCGGAGCTGCGCCTCG CCGCTTGCTGGCGAAGCT C PSMD5 Ensembl:ENSG00000095261 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:120842769..120842907 26863196 MeRIP-seq:(Medium) rs775811039 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_5036356,Human_RBP_ID_18427204,Human_RBP_ID_22119344,Human_RBP_ID_26833446 Human_Splice_Rec_1076105,Human_Splice_Rec_1076123,Human_Splice_Rec_1076143,Human_Splice_Rec_1076147,Human_Splice_Rec_1076151 RMVar_hsa_circ_90631,RMVar_hsa_circ_259124,RMVar_hsa_circ_127217,RMVar_hsa_circ_259136 106991 RMVar_ID_106991 Human_SNP_ID_414006040 m1A Human chr9 - 120856050 120856050 120856050 ACCCCTAGCCCAGGGGTGCTGTGGGAACTGGGATCCAATTTGTAGCTTCCTGCCTGGCTTCAGAG ACCCCTAGCCCAGGGGTGCTGTGGGAACTGGGTTCCAATTTGTAGCTTCCTGCCTGGCTTCAGAG T A PHF19 Ensembl:ENSG00000119403 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:120856000..120856201 32194978 MeRIP-seq:(Medium) rs1048652472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95988,RMVar_hsa_circ_259140 106992 RMVar_ID_106992 Human_SNP_ID_414006351 m1A Human chr9 + 120857394 120857394 120857394 GGGGCTCTCTCCCATCCCACCACCTCTCTCCGAGGGTAGTGGGGAGTGGCAGGAAAGTGGAAGAG GGGGCTCTCTCCCATCCCACCACCTCTCTCCGGGGGTAGTGGGGAGTGGCAGGAAAGTGGAAGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:120857346..120857447 32194978 MeRIP-seq:(Medium) rs901269724 Functional Loss SNV dbSNP153 33..33 33 - - - 106993 RMVar_ID_106993 Human_SNP_ID_414009754 m1A Human chr9 - 120869925 120869925 120869925 CCTCTGCCGTAGGTTACCACCAGCAGTGCCACATCCCCATAGCGGGCAGTGCTGACCAGCCCCTG CCTCTGCCGTAGGTTACCACCAGCAGTGCCACGTCCCCATAGCGGGCAGTGCTGACCAGCCCCTG T C PHF19 Ensembl:ENSG00000119403 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:120869800..120869995 26863196 MeRIP-seq:(Medium) rs1335340389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974744,Human_RBP_ID_22517660,Human_RBP_ID_26833458 Human_Splice_Rec_1076236,Human_Splice_Rec_1076237,Human_Splice_Rec_1076282,Human_Splice_Rec_1076283,Human_Splice_Rec_1076366,Human_Splice_Rec_1076367,Human_Splice_Rec_1076376 RMVar_hsa_circ_3009,RMVar_hsa_circ_112733,RMVar_hsa_circ_259146,RMVar_hsa_circ_77816,RMVar_hsa_circ_259149,RMVar_hsa_circ_94110,RMVar_hsa_circ_111220,RMVar_hsa_circ_259147,RMVar_hsa_circ_101488,RMVar_hsa_circ_259150,RMVar_hsa_circ_259148 106994 RMVar_ID_106994 Human_SNP_ID_414011019 m1A Human chr9 - 120874674 120874674 120874674 CTCCTATGGTGCCACCAGCCACCTCCCCAACAAGGGGGCCCTGGCGAAGGTCAAGAACAACTTCA CTCCTATGGTGCCACCAGCCACCTCCCCAACAGGGGGGCCCTGGCGAAGGTCAAGAACAACTTCA T C PHF19 Ensembl:ENSG00000119403 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:120874651..120874675 26863196 MeRIP-seq:(Medium) rs146513217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797271,Human_RBP_ID_17666347,Human_RBP_ID_22517662 Human_Splice_Rec_1076230,Human_Splice_Rec_1076276,Human_Splice_Rec_1076360,Human_Splice_Rec_1076370,Human_Splice_Rec_1076378 Human_miRNA_ID_2295417,Human_miRNA_ID_2295418,Human_miRNA_ID_2573200,Human_miRNA_ID_2573201 RMVar_hsa_circ_112733,RMVar_hsa_circ_259146,RMVar_hsa_circ_77816,RMVar_hsa_circ_259147,RMVar_hsa_circ_101488,RMVar_hsa_circ_259148,RMVar_hsa_circ_373116,RMVar_hsa_circ_259152 106995 RMVar_ID_106995 Human_SNP_ID_414011044 m1A Human chr9 + 120874754 120874754 120874754 TCCAGAGCTCGATTCTCCATCAGCTTCCCCTGACACTGGGAGAGAAAGAACAGGGTTTTTGCTTC TCCAGAGCTCGATTCTCCATCAGCTTCCCCTGCCACTGGGAGAGAAAGAACAGGGTTTTTGCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:120874519..120875989 26863196 MeRIP-seq:(Medium) rs781300971 Functional Loss SNV dbSNP153 33..33 33 - - - 106996 RMVar_ID_106996 Human_SNP_ID_414011173 m1A Human chr9 + 120875408 120875408 120875408 ATTTGCTCCAAGCAGTGAAGTCATCCATCCCCATGCCAGCCTCTCCACGCCTGTCTCTCACCATC ATTTGCTCCAAGCAGTGAAGTCATCCATCCCCGTGCCAGCCTCTCCACGCCTGTCTCTCACCATC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120875402..120875622 26863196 MeRIP-seq:(Medium) rs1361460351 Functional Loss SNV dbSNP153 33..33 33 - - - 106997 RMVar_ID_106997 Human_SNP_ID_414011697 m1A Human chr9 - 120877164 120877164 120877164 GGGCGGACACTCGGCCGGGCAGCCGCGGGCCGAGCGCAGCCGCCTCCGCCACCGATGCGCCTGGT GGGCGGACACTCGGCCGGGCAGCCGCGGGCCGGGCGCAGCCGCCTCCGCCACCGATGCGCCTGGT T C PHF19 Ensembl:ENSG00000119403 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:120877024..120877350 26863196 MeRIP-seq:(Medium) rs1364749437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_710473,Human_RBP_ID_5036360,Human_RBP_ID_5154448,Human_RBP_ID_9339029 Human_Splice_Rec_1076229,Human_Splice_Rec_1076369 106998 RMVar_ID_106998 Human_SNP_ID_414011746 m1A Human chr9 + 120877256 120877256 120877256 GGGCGGGGCGGGGCGGGGGCGCCGCGGGGAGGAGGGGGAGGCGGCGGAGGGAGGGGCCGGGGCGC GGGCGGGGCGGGGCGGGGGCGCCGCGGGGAGGGGGGGGAGGCGGCGGAGGGAGGGGCCGGGGCGC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:120877154..120877313 26863410 MeRIP-seq:(Medium) rs1178143861 Functional Loss SNV dbSNP153 33..33 33 - - - 106999 RMVar_ID_106999 Human_SNP_ID_414024071 m1A Human chr9 - 120927896 120927896 120927896 AGAAGTCTTGGGTGCCTGTTTTATCCCAAACCAGGGGAAGGAGGGAACAGGTAGGGCTGGCTGCA AGAAGTCTTGGGTGCCTGTTTTATCCCAAACCGGGGGAAGGAGGGAACAGGTAGGGCTGGCTGCA T C TRAF1 Ensembl:ENSG00000056558 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:120927846..120927994 26863196 MeRIP-seq:(Medium) rs926050308 Functional Loss SNV dbSNP153 33..33 33 - - - 107000 RMVar_ID_107000 Human_SNP_ID_414045949 m1A Human chr9 + 121024306 121024299 121024306 GGGGGAGGGGAGGGGGAGGGGAGGGGAGCGGGAGGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG GGGGGAGGGGAGGGGGAGGGGAGGGG_______GGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG GAGCGGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:121024194..121024321 26863196 MeRIP-seq:(Medium) rs1564156707 Functional Loss DEL dbSNP153 27..33 33 - - - 107001 RMVar_ID_107001 Human_SNP_ID_414045956 m1A Human chr9 + 121024306 121024301 121024306 GGGGGAGGGGAGGGGGAGGGGAGGGGAGCGGGAGGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG GGGGGAGGGGAGGGGGAGGGGAGGGGAG_____GGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG GCGGGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:121024194..121024321 26863196 MeRIP-seq:(Medium) rs1564156727 Functional Loss DEL dbSNP153 29..33 33 - - - 107002 RMVar_ID_107002 Human_SNP_ID_414045962 m1A Human chr9 + 121024306 121024306 121024306 GGGGGAGGGGAGGGGGAGGGGAGGGGAGCGGGAGGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG GGGGGAGGGGAGGGGGAGGGGAGGGGAGCGGGGGGGGGGAGGGGGAGGGGAGGGGGAGGGGAGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:121024194..121024321 26863196 MeRIP-seq:(Medium) rs1285578365 Functional Loss SNV dbSNP153 33..33 33 - - - 107003 RMVar_ID_107003 Human_SNP_ID_414058039 m1A Human chr9 + 121076615 121076615 121076615 AGAAATGTTGAGTCTGGGCACAGGAAAGAACCATAGAGAAATGGGGGAGACTATTACTGTGTTAG AGAAATGTTGAGTCTGGGCACAGGAAAGAACCGTAGAGAAATGGGGGAGACTATTACTGTGTTAG A G CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121076451..121076693 26863196 MeRIP-seq:(Medium) rs924280872 Functional Loss SNV dbSNP153 33..33 33 - - - 107004 RMVar_ID_107004 Human_SNP_ID_414058040 m1A Human chr9 + 121076615 121076615 121076615 AGAAATGTTGAGTCTGGGCACAGGAAAGAACCATAGAGAAATGGGGGAGACTATTACTGTGTTAG AGAAATGTTGAGTCTGGGCACAGGAAAGAACCTTAGAGAAATGGGGGAGACTATTACTGTGTTAG A T CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121076451..121076693 26863196 MeRIP-seq:(Medium) rs924280872 Functional Loss SNV dbSNP153 33..33 33 - - - 107005 RMVar_ID_107005 Human_SNP_ID_414075444 m1A Human chr9 + 121147634 121147634 121147634 GAAGTGAGGAGAAGACTGGGGCCTGAATGTTGAAAGTGAGGAGAAGACTATAGGCTGTATTCATC GAAGTGAGGAGAAGACTGGGGCCTGAATGTTGGAAGTGAGGAGAAGACTATAGGCTGTATTCATC A G CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121147590..121147655 26863196 MeRIP-seq:(Medium) rs1357364960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16554353 RMVar_hsa_circ_69378,RMVar_hsa_circ_112631,RMVar_hsa_circ_259170,RMVar_hsa_circ_89896,RMVar_hsa_circ_27980,RMVar_hsa_circ_24896,RMVar_hsa_circ_106751,RMVar_hsa_circ_259171,RMVar_hsa_circ_43533,RMVar_hsa_circ_259173,RMVar_hsa_circ_54128,RMVar_hsa_circ_266585,RMVar_hsa_circ_103730,RMVar_hsa_circ_51844,RMVar_hsa_circ_322528,RMVar_hsa_circ_259175,RMVar_hsa_circ_340995,RMVar_hsa_circ_364729,RMVar_hsa_circ_335150,RMVar_hsa_circ_49387,RMVar_hsa_circ_268353,RMVar_hsa_circ_259176 107006 RMVar_ID_107006 Human_SNP_ID_414088839 m1A Human chr9 + 121201761 121201761 121201761 CGGGGGCGGTCGACCGAGGCGCCGGCAGGTACACTGGCAGGCCGAGAGGTGCAGACGCGCCGGCA CGGGGGCGGTCGACCGAGGCGCCGGCAGGTACTCTGGCAGGCCGAGAGGTGCAGACGCGCCGGCA A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:121201718..121201835 26863196 MeRIP-seq:(Medium) rs1564325466 Functional Loss SNV dbSNP153 33..33 33 - - - 107007 RMVar_ID_107007 Human_SNP_ID_414088869 m1A Human chr9 - 121201822 121201822 121201822 GAGGAAGATACTGAGGGAGCACAGGAGCAGTCACCGCTGCCACTGCTACTGCCGCTACTGCTGCC GAGGAAGATACTGAGGGAGCACAGGAGCAGTCCCCGCTGCCACTGCTACTGCCGCTACTGCTGCC T G RAB14 Ensembl:ENSG00000119396 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:121201626..121201900 26863196 MeRIP-seq:(Medium) rs888394229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184485,Human_RBP_ID_1701554,Human_RBP_ID_5007997,Human_RBP_ID_7893013,Human_RBP_ID_17437183,Human_RBP_ID_17715769,Human_RBP_ID_18427208 107008 RMVar_ID_107008 Human_SNP_ID_414103331 m1A Human chr9 + 121268218 121268218 121268218 CCAGCAGCCGCTGTCTCCAGTGCCGCAGCAGCAGGTAGGGGAGGCGCGCGGCCCCGGCCCCGGGC CCAGCAGCCGCTGTCTCCAGTGCCGCAGCAGCGGGTAGGGGAGGCGCGCGGCCCCGGCCCCGGGC A G GSN Ensembl:ENSG00000148180 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:121268176..121268272;chr9:121268213..121268340;chr9:121268151..121268269;chr9:121268168..121268271;chr9:121268190..121268277 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs571917464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036362 Human_Splice_Rec_1077031,Human_Splice_Rec_1077045,Human_Splice_Rec_1077081,Human_Splice_Rec_1077089 RMVar_hsa_circ_340276,RMVar_hsa_circ_110682,RMVar_hsa_circ_259198 107009 RMVar_ID_107009 Human_SNP_ID_414106857 m1A Human chr9 + 121283908 121283908 121283908 GTGGGAGTGGTGAGGTCTTATCTGGACAGATCAGGGAAGCCTCCCCTAAAAAGTGAGACCTGAAG GTGGGAGTGGTGAGGTCTTATCTGGACAGATCGGGGAAGCCTCCCCTAAAAAGTGAGACCTGAAG A G GSN Ensembl:ENSG00000148180 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121283904..121284120 26863196 MeRIP-seq:(Medium) rs1156892318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16555387 RMVar_hsa_circ_49928 107010 RMVar_ID_107010 Human_SNP_ID_414111178 m1A Human chr9 - 121302044 121302020 121302044 ATAAAGGTTGGTGGGCACGGGCACCAGATCGAACTTCTCCACACGCCAGATCTGCAGGCCAGGCT ATAAAGGTTGGTGGGCACGGGCACCAGATCGA________________________GGCCAGGCT CTGCAGATCTGGCGTGTGGAGAAGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:121301995..121302077 26863196 MeRIP-seq:(Medium) rs771479527 Functional Loss DEL dbSNP153 33..56 33 - - - 107011 RMVar_ID_107011 Human_SNP_ID_414117345 m1A Human chr9 - 121326454 121326454 121326454 CAGGGACCTTGGGGGCAGGCTTCAGTCCTTCTATGTCGCACTGGGCCCATCCCTCCAGACGAAGC CAGGGACCTTGGGGGCAGGCTTCAGTCCTTCTGTGTCGCACTGGGCCCATCCCTCCAGACGAAGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:121326401..121326550 26863196 MeRIP-seq:(Medium) rs771747913 Functional Loss SNV dbSNP153 33..33 33 - - - 107012 RMVar_ID_107012 Human_SNP_ID_414117485 m1A Human chr9 - 121326738 121326738 121326738 CCCCGTTCCTGTGCCTGGAGATCTGGTCATTGAGCTGGGAGGTTTCAGGGAGGCCAATCCCTTCT CCCCGTTCCTGTGCCTGGAGATCTGGTCATTGGGCTGGGAGGTTTCAGGGAGGCCAATCCCTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:121326687..121326826 26863196 MeRIP-seq:(Medium) rs377210790 Functional Loss SNV dbSNP153 33..33 33 - - - 107013 RMVar_ID_107013 Human_SNP_ID_414117521 m1A Human chr9 - 121326794 121326794 121326794 CCACGGCAGGAAAATACAAAAAGCTGCTTCTTACCCCGTCATTCACCATCCCCTGCCCCCGTTCC CCACGGCAGGAAAATACAAAAAGCTGCTTCTTGCCCCGTCATTCACCATCCCCTGCCCCCGTTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:121326651..121326821;chr9:121326651..121326841 26863196 MeRIP-seq:(Medium) rs751568419 Functional Loss SNV dbSNP153 33..33 33 - - - 107014 RMVar_ID_107014 Human_SNP_ID_414123485 m1A Human chr9 + 121353529 121353529 121353529 GGAGTTCATTTCCTTAATCTACTGTTGCTATCACTCTTCTCCCCACCGCCCCACTGGGACCAATG GGAGTTCATTTCCTTAATCTACTGTTGCTATCGCTCTTCTCCCCACCGCCCCACTGGGACCAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:121353523..121353769 26863196 MeRIP-seq:(Medium) rs891180297 Functional Loss SNV dbSNP153 33..33 33 - - - 107015 RMVar_ID_107015 Human_SNP_ID_414124192 m1A Human chr9 - 121356156 121356156 121356156 TGTGAGAGTTGTATATTTTTTGTTTTCAACAGACAGCCCCAGTAAGGGCCTTGGACCTTGCGGAT TGTGAGAGTTGTATATTTTTTGTTTTCAACAGGCAGCCCCAGTAAGGGCCTTGGACCTTGCGGAT T C STOM Ensembl:ENSG00000148175 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:121356140..121356211 26863196 MeRIP-seq:(Medium) rs772615715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965532,Human_RBP_ID_5036364 Human_Splice_Rec_1077284,Human_Splice_Rec_1077296,Human_Splice_Rec_1077304 RMVar_hsa_circ_107614,RMVar_hsa_circ_364252,RMVar_hsa_circ_259205,RMVar_hsa_circ_68790,RMVar_hsa_circ_361149 107016 RMVar_ID_107016 Human_SNP_ID_414127281 m1A Human chr9 - 121370190 121370190 121370190 CGAGGACGGGGGAGTGCGACTGCGTCTCGGGCAGCATGGCCGAGAAGCGGCACACACGGGACTCC CGAGGACGGGGGAGTGCGACTGCGTCTCGGGCCGCATGGCCGAGAAGCGGCACACACGGGACTCC T G STOM Ensembl:ENSG00000148175 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:121370062..121370250;chr9:121370081..121370226 26863196 MeRIP-seq:(Medium) rs1269047832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847088,Human_RBP_ID_965533,Human_RBP_ID_5035845,Human_RBP_ID_5330029,Human_RBP_ID_22466554 Human_Splice_Rec_1077283,Human_Splice_Rec_1077295,Human_Splice_Rec_1077303 RMVar_hsa_circ_107614,RMVar_hsa_circ_259205 107017 RMVar_ID_107017 Human_SNP_ID_414127294 m1A Human chr9 - 121370210 121370210 121370210 GGCGGCTCCGGGTTTGGCAACGAGGACGGGGGAGTGCGACTGCGTCTCGGGCAGCATGGCCGAGA GGCGGCTCCGGGTTTGGCAACGAGGACGGGGGGGTGCGACTGCGTCTCGGGCAGCATGGCCGAGA T C STOM Ensembl:ENSG00000148175 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:121369989..121370250 26863196 MeRIP-seq:(Medium) rs574837646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797609,Human_RBP_ID_847088,Human_RBP_ID_5035845,Human_RBP_ID_5330029,Human_RBP_ID_22466554 Human_Splice_Rec_1077283,Human_Splice_Rec_1077295,Human_Splice_Rec_1077303 RMVar_hsa_circ_107614,RMVar_hsa_circ_259205 107018 RMVar_ID_107018 Human_SNP_ID_414161978 m1A Human chr9 - 121519886 121519886 121519886 GAAAAAGAAGGAAGAGGAGGAAGATGAGGAAGACGAAGAGGATGAGGAGGAGGAGGAAGATGAAG GAAAAAGAAGGAAGAGGAGGAAGATGAGGAAGGCGAAGAGGATGAGGAGGAGGAGGAAGATGAAG T C HMGB1P37 Ensembl:ENSG00000213467 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:121519835..121519919 26863196 MeRIP-seq:(Medium) rs1164805080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3911455,Human_RBP_ID_5008033,Human_RBP_ID_5107201,Human_RBP_ID_7893065,Human_RBP_ID_8275361,Human_RBP_ID_18542338,Human_RBP_ID_24282509 107019 RMVar_ID_107019 Human_SNP_ID_414215893 m1A Human chr9 + 121739267 121739266 121739267 CAAGAACTCCTAGCCTAGGGAGCAGCAAGTACAAAGTCCTTGAGCAGGAAACAGAGACTTTGGTG CAAGAACTCCTAGCCTAGGGAGCAGCAAGTAC_AAGTCCTTGAGCAGGAAACAGAGACTTTGGTG CA C DAB2IP Ensembl:ENSG00000136848 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:121739248..121739637 26863196 MeRIP-seq:(Medium) rs1219816969 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_60047 107020 RMVar_ID_107020 Human_SNP_ID_414215952 m1A Human chr9 - 121739479 121739479 121739479 ACCACTGGGCTTCCCCTTACCCCTACCAGGGGAGTCAGAGGGACCCTTCAGAAATGCAAATCAGA ACCACTGGGCTTCCCCTTACCCCTACCAGGGGTGTCAGAGGGACCCTTCAGAAATGCAAATCAGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121739470..121739662 26863196 MeRIP-seq:(Medium) rs180905592 Functional Loss SNV dbSNP153 33..33 33 - - - 107021 RMVar_ID_107021 Human_SNP_ID_414216052 m1A Human chr9 + 121739852 121739852 121739852 TGGAAAGAATCACCAAAGGAAAGTGTTGTGCTAAGGAAGTGTCTCCGAAACAGCCCTGAGGAGCT TGGAAAGAATCACCAAAGGAAAGTGTTGTGCTGAGGAAGTGTCTCCGAAACAGCCCTGAGGAGCT A G DAB2IP Ensembl:ENSG00000136848 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:121739850..121740162 26863196 MeRIP-seq:(Medium) rs758910142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60047 107022 RMVar_ID_107022 Human_SNP_ID_414227914 m1A Human chr9 + 121782395 121782393 121782395 TGCCCGCCTCATGAGTGCCCTGACCCAGCTGAAAGAGAGGTACAGCATGCAAGCCCGTAACGGCA TGCCCGCCTCATGAGTGCCCTGACCCAGCTG__AGAGAGGTACAGCATGCAAGCCCGTAACGGCA GAA G DAB2IP Ensembl:ENSG00000136848 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:121782344..121782554 26863196 MeRIP-seq:(Medium) rs1335686410 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9407343 Human_Splice_Rec_1077430,Human_Splice_Rec_1077431,Human_Splice_Rec_1077464,Human_Splice_Rec_1077492,Human_Splice_Rec_1077493,Human_Splice_Rec_1077520,Human_Splice_Rec_1077546 RMVar_hsa_circ_60047,RMVar_hsa_circ_259213,RMVar_hsa_circ_116047 107023 RMVar_ID_107023 Human_SNP_ID_414228807 m1A Human chr9 + 121785165 121785165 121785165 ACTCTTTCCGACTGCCCAGAAAGTGGGGGTGGAGGACCGAGGCTACAGCTCCACACGCCCCGGTC ACTCTTTCCGACTGCCCAGAAAGTGGGGGTGGTGGACCGAGGCTACAGCTCCACACGCCCCGGTC A T DAB2IP Ensembl:ENSG00000136848 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:121784683..121785281 32194978 MeRIP-seq:(Medium) rs1189420409 Functional Loss SNV dbSNP153 33..33 33 - - - 107024 RMVar_ID_107024 Human_SNP_ID_414228848 m1A Human chr9 + 121785241 121785241 121785241 CTGCCCCAGGTACACCTCCCCCTGCGCCCCGCACGACTGCGGGAGCCAGACTGTCCAGGGAAACA CTGCCCCAGGTACACCTCCCCCTGCGCCCCGCGCGACTGCGGGAGCCAGACTGTCCAGGGAAACA A G DAB2IP Ensembl:ENSG00000136848 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121785192..121785329 26863196 MeRIP-seq:(Medium) rs1307745362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1549741,Human_miRNA_ID_1550248 107025 RMVar_ID_107025 Human_SNP_ID_414278459 m1A Human chr9 + 121987885 121987885 121987885 CATTTGCTGATGAGTTCTCATCTCTGTCCCCAACCCAGGCCTCTGTCTCCTGAACTCCAAGCTCC CATTTGCTGATGAGTTCTCATCTCTGTCCCCAGCCCAGGCCTCTGTCTCCTGAACTCCAAGCTCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:121987881..121988010 26863196 MeRIP-seq:(Medium) rs998184969 Functional Loss SNV dbSNP153 33..33 33 - - - 107026 RMVar_ID_107026 Human_SNP_ID_414318564 m1A Human chr9 - 122159720 122159720 122159720 GGTCGAAAGGGGAGTTCAAGGAGACGGGGGCGACGCGGCTGAGGGCTTCTCGTCGGGGTCGGGGC GGTCGAAAGGGGAGTTCAAGGAGACGGGGGCGTCGCGGCTGAGGGCTTCTCGTCGGGGTCGGGGC T A NDUFA8 Ensembl:ENSG00000119421 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr9:122152291..122159800;chr9:122159623..122159751;chr9:122159585..122159722;chr9:122159587..122159800 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1344462950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452,Human_RBP_ID_255867,Human_RBP_ID_797274,Human_RBP_ID_847364,Human_RBP_ID_5008183,Human_RBP_ID_5330030,Human_RBP_ID_5430902,Human_RBP_ID_5481665,Human_RBP_ID_18427209,Human_RBP_ID_26362040 Human_Splice_Rec_1077623 RMVar_hsa_circ_259223,RMVar_hsa_circ_87981 107027 RMVar_ID_107027 Human_SNP_ID_414318573 m1A Human chr9 - 122159729 122159728 122159730 GCACTCGGCGGTCGAAAGGGGAGTTCAAGGAGACGGGGGCGACGCGGCTGAGGGCTTCTCGTCGG GCACTCGGCGGTCGAAAGGGGAGTTCAAGGA__CGGGGGCGACGCGGCTGAGGGCTTCTCGTCGG GTC G NDUFA8 Ensembl:ENSG00000119421 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:122148176..122159800 26863196 MeRIP-seq:(Medium) rs748713851 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_255867,Human_RBP_ID_797274,Human_RBP_ID_847364,Human_RBP_ID_5036368,Human_RBP_ID_5430902,Human_RBP_ID_18427209 RMVar_hsa_circ_259223,RMVar_hsa_circ_87981 107028 RMVar_ID_107028 Human_SNP_ID_414318575 m1A Human chr9 - 122159729 122159729 122159729 GCACTCGGCGGTCGAAAGGGGAGTTCAAGGAGACGGGGGCGACGCGGCTGAGGGCTTCTCGTCGG GCACTCGGCGGTCGAAAGGGGAGTTCAAGGAGGCGGGGGCGACGCGGCTGAGGGCTTCTCGTCGG T C NDUFA8 Ensembl:ENSG00000119421 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:122148176..122159800 26863196 MeRIP-seq:(Medium) rs767773124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255867,Human_RBP_ID_797274,Human_RBP_ID_847364,Human_RBP_ID_5036368,Human_RBP_ID_5430902,Human_RBP_ID_18427209 RMVar_hsa_circ_259223,RMVar_hsa_circ_87981 107029 RMVar_ID_107029 Human_SNP_ID_414343999 m1A Human chr9 - 122264788 122264788 122264788 TGGCAGCTGGCGGCATTGAGGCGGACGCGTCTAGAGGTCCGTCTGACCGCGGCGTCGGGACCTGG TGGCAGCTGGCGGCATTGAGGCGGACGCGTCTGGAGGTCCGTCTGACCGCGGCGTCGGGACCTGG T C RBM18 Ensembl:ENSG00000119446 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:122264675..122264850 26863196 MeRIP-seq:(Medium) rs1234812372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036372,Human_RBP_ID_17437185 Human_Splice_Rec_1077769,Human_Splice_Rec_1077785 107030 RMVar_ID_107030 Human_SNP_ID_414344007 m1A Human chr9 - 122264796 122264796 122264796 GGGCGGCCTGGCAGCTGGCGGCATTGAGGCGGACGCGTCTAGAGGTCCGTCTGACCGCGGCGTCG GGGCGGCCTGGCAGCTGGCGGCATTGAGGCGGGCGCGTCTAGAGGTCCGTCTGACCGCGGCGTCG T C RBM18 Ensembl:ENSG00000119446 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:122261423..122264850;chr9:122261432..122264850 26863196 MeRIP-seq:(Medium) rs1419253924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036372,Human_RBP_ID_17437185 Human_Splice_Rec_1077769,Human_Splice_Rec_1077785 107031 RMVar_ID_107031 Human_SNP_ID_414351914 m1A Human chr9 + 122298951 122298951 122298951 AGAGGAAGGTGATACTTGCAGAGAATTGAGGGATGTACAAGAACAAACCATGCCTATATCCAGCA AGAGGAAGGTGATACTTGCAGAGAATTGAGGGGTGTACAAGAACAAACCATGCCTATATCCAGCA A G MRRF Ensembl:ENSG00000148187 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:122298929..122298994 26863196 MeRIP-seq:(Medium) rs1269469381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16556207 RMVar_hsa_circ_259226,RMVar_hsa_circ_121347,RMVar_hsa_circ_17921,RMVar_hsa_circ_301049,RMVar_hsa_circ_24651,RMVar_hsa_circ_259230,RMVar_hsa_circ_313148,RMVar_hsa_circ_90445,RMVar_hsa_circ_259239 107032 RMVar_ID_107032 Human_SNP_ID_414368781 m1A Human chr9 - 122371093 122371093 122371093 AAAATTCCCCACCGGGCACCGGGGTCGCACTCACGGCTCATGGCGCGGCTGCTGGGGTGCGGGAC AAAATTCCCCACCGGGCACCGGGGTCGCACTCGCGGCTCATGGCGCGGCTGCTGGGGTGCGGGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:122371051..122371307;chr9:122371054..122371138;chr9:122371068..122371161 26863196 MeRIP-seq:(Medium) rs1191236607 Functional Loss SNV dbSNP153 33..33 33 - - - 107033 RMVar_ID_107033 Human_SNP_ID_414370943 m1A Human chr9 - 122378907 122378907 122378907 CAGCTCCTCACCCCATTTTACCTTTGGTTCCCATGGGTGTGGGGCAATCTTTAGGCACAGAGGGC CAGCTCCTCACCCCATTTTACCTTTGGTTCCCGTGGGTGTGGGGCAATCTTTAGGCACAGAGGGC T C lnc-OR1J1-2 RNACentral:URS0000D5C4CF lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:122378753..122378958 26863196 MeRIP-seq:(Medium) rs1195588804 Functional Loss SNV dbSNP153 33..33 33 - - - 107034 RMVar_ID_107034 Human_SNP_ID_414374644 m1A Human chr9 + 122392535 122392535 122392535 GATGATGGGCCTGCTGTGGAGCGACCATCCACAGAGCTCTGAGGGGCAGGAAAGCAGCATTCTGG GATGATGGGCCTGCTGTGGAGCGACCATCCACGGAGCTCTGAGGGGCAGGAAAGCAGCATTCTGG A G PTGS1 Ensembl:ENSG00000095303 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:122392346..122392625 26863196 MeRIP-seq:(Medium) rs766010151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22119350 107035 RMVar_ID_107035 Human_SNP_ID_414478987 m1A Human chr9 - 122820599 122820599 122820599 TCTGAAGGAGTTTGCCATAATGAATGAGGACCAAGATGATGAAGAGTTTCTGCAGCAGTACCGGA TCTGAAGGAGTTTGCCATAATGAATGAGGACCGAGATGATGAAGAGTTTCTGCAGCAGTACCGGA T C PDCL Ensembl:ENSG00000136940 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:122820551..122820690 26863196 MeRIP-seq:(Medium) rs771893986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92495,Human_RBP_ID_1701610,Human_RBP_ID_7893554,Human_RBP_ID_8709362,Human_RBP_ID_9407348,Human_RBP_ID_16556601,Human_RBP_ID_18128904,Human_RBP_ID_18902991,Human_RBP_ID_26736140,Human_RBP_ID_27541725 Human_Splice_Rec_1078168 Human_miRNA_ID_247194,Human_miRNA_ID_249729 107036 RMVar_ID_107036 Human_SNP_ID_414478988 m1A Human chr9 - 122820599 122820599 122820599 TCTGAAGGAGTTTGCCATAATGAATGAGGACCAAGATGATGAAGAGTTTCTGCAGCAGTACCGGA TCTGAAGGAGTTTGCCATAATGAATGAGGACCCAGATGATGAAGAGTTTCTGCAGCAGTACCGGA T G PDCL Ensembl:ENSG00000136940 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:122820551..122820690 26863196 MeRIP-seq:(Medium) rs771893986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92495,Human_RBP_ID_1701610,Human_RBP_ID_7893554,Human_RBP_ID_8709362,Human_RBP_ID_9407348,Human_RBP_ID_16556601,Human_RBP_ID_18128904,Human_RBP_ID_18902991,Human_RBP_ID_26736140,Human_RBP_ID_27541725 Human_Splice_Rec_1078168 Human_miRNA_ID_247194,Human_miRNA_ID_249729 107037 RMVar_ID_107037 Human_SNP_ID_414481035 m1A Human chr9 + 122828414 122828414 122828414 AAGGGGCAGTTTTACCCAAGCTCGCCAACCCCACTCCCTCCCGTAGTCCGCAGCTGCTGCCGCTT AAGGGGCAGTTTTACCCAAGCTCGCCAACCCCGCTCCCTCCCGTAGTCCGCAGCTGCTGCCGCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:122828412..122828531 26863196 MeRIP-seq:(Medium) rs575578845 Functional Loss SNV dbSNP153 33..33 33 - - - 107038 RMVar_ID_107038 Human_SNP_ID_414547188 m1A Human chr9 + 123086772 123086772 123086772 AGGGTGAAGACTGGGAAAAGACTGAGCTGGTGAAGAAGTCAGGACTCTGGACCAGCAAAGTCTGT AGGGTGAAGACTGGGAAAAGACTGAGCTGGTGTAGAAGTCAGGACTCTGGACCAGCAAAGTCTGT A T RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123086763..123086863 26863196 MeRIP-seq:(Medium) rs753788322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7894547,Human_RBP_ID_23300592 RMVar_hsa_circ_64354,RMVar_hsa_circ_126303,RMVar_hsa_circ_259294,RMVar_hsa_circ_103323,RMVar_hsa_circ_259297,RMVar_hsa_circ_26012,RMVar_hsa_circ_360798,RMVar_hsa_circ_349048,RMVar_hsa_circ_259310,RMVar_hsa_circ_259317,RMVar_hsa_circ_259321,RMVar_hsa_circ_280585,RMVar_hsa_circ_302908,RMVar_hsa_circ_316092,RMVar_hsa_circ_259319,RMVar_hsa_circ_259320,RMVar_hsa_circ_259318,RMVar_hsa_circ_259323,RMVar_hsa_circ_329935,RMVar_hsa_circ_305593,RMVar_hsa_circ_84294,RMVar_hsa_circ_259322,RMVar_hsa_circ_281243,RMVar_hsa_circ_265278,RMVar_hsa_circ_259325,RMVar_hsa_circ_109779,RMVar_hsa_circ_259328,RMVar_hsa_circ_259326 107039 RMVar_ID_107039 Human_SNP_ID_414547193 m1A Human chr9 + 123086809 123086791 123086809 GTCAGGACTCTGGACCAGCAAAGTCTGTGAAGACAGCAGAGCTTTGTGTACACCCGTTCCTGAGA GTCAGGACTCTGGAC__________________CAGCAGAGCTTTGTGTACACCCGTTCCTGAGA CCAGCAAAGTCTGTGAAGA C RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:123086758..123086856 26863196 MeRIP-seq:(Medium) rs1417958091 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_16559777,Human_RBP_ID_23300592 RMVar_hsa_circ_64354,RMVar_hsa_circ_126303,RMVar_hsa_circ_259294,RMVar_hsa_circ_103323,RMVar_hsa_circ_259297,RMVar_hsa_circ_26012,RMVar_hsa_circ_360798,RMVar_hsa_circ_349048,RMVar_hsa_circ_259310,RMVar_hsa_circ_259317,RMVar_hsa_circ_259321,RMVar_hsa_circ_280585,RMVar_hsa_circ_302908,RMVar_hsa_circ_316092,RMVar_hsa_circ_259319,RMVar_hsa_circ_259320,RMVar_hsa_circ_259318,RMVar_hsa_circ_259323,RMVar_hsa_circ_329935,RMVar_hsa_circ_305593,RMVar_hsa_circ_84294,RMVar_hsa_circ_259322,RMVar_hsa_circ_281243,RMVar_hsa_circ_265278,RMVar_hsa_circ_259325,RMVar_hsa_circ_109779,RMVar_hsa_circ_259328,RMVar_hsa_circ_259326 107040 RMVar_ID_107040 Human_SNP_ID_414554231 m1A Human chr9 - 123114723 123114723 123114723 CAATAGAGGGAACAATGGTGTTTCTGACCAGGACGGGGGAAGGCAGGGGAATGGAGGAAGATACT CAATAGAGGGAACAATGGTGTTTCTGACCAGGGCGGGGGAAGGCAGGGGAATGGAGGAAGATACT T C MIR600HG,STRBP Ensembl:ENSG00000236901,Ensembl:ENSG00000165209 lincRNA,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123114678..123114763 26863196 MeRIP-seq:(Medium) rs921410309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5230188,Human_RBP_ID_7894650,Human_RBP_ID_8226321,Human_RBP_ID_18903139 107041 RMVar_ID_107041 Human_SNP_ID_414558240 m1A Human chr9 + 123132924 123132924 123132924 CTTGTTAGAGTTCCTCTTCCTCTGCCCCGAACAGCTTGGACTGCTGCAGACACAGCTGTATTCAC CTTGTTAGAGTTCCTCTTCCTCTGCCCCGAACGGCTTGGACTGCTGCAGACACAGCTGTATTCAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:123132876..123132925 32194978 MeRIP-seq:(Medium) rs1363108524 Functional Loss SNV dbSNP153 33..33 33 - - - 107042 RMVar_ID_107042 Human_SNP_ID_414576369 m1A Human chr9 + 123213856 123213856 123213856 CCGAGGCAGAATTGCTTGAACCTGGGAGGCGGAGATTGCAGTGAGCCGAGATTGCGCCACTGTAC CCGAGGCAGAATTGCTTGAACCTGGGAGGCGGGGATTGCAGTGAGCCGAGATTGCGCCACTGTAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123213853..123213933 26863196 MeRIP-seq:(Medium) rs765966542 Functional Loss SNV dbSNP153 33..33 33 - - - 107043 RMVar_ID_107043 Human_SNP_ID_414589439 m1A Human chr9 - 123268509 123268509 123268509 GCAGCCGCCGCCGCTGGGCAGAGGAGCCGGAGACGCGAGCGGGCGAGGTGGCGGCGGCGGCGGAG GCAGCCGCCGCCGCTGGGCAGAGGAGCCGGAGGCGCGAGCGGGCGAGGTGGCGGCGGCGGCGGAG T C STRBP Ensembl:ENSG00000165209 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:123268376..123268557 26863196 MeRIP-seq:(Medium) rs1169555550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036383,Human_RBP_ID_5482505,Human_RBP_ID_9355052,Human_RBP_ID_9408485,Human_RBP_ID_17672556,Human_RBP_ID_18427371 Human_Splice_Rec_1078573,Human_Splice_Rec_1078641,Human_Splice_Rec_1078677 107044 RMVar_ID_107044 Human_SNP_ID_414618722 m1A Human chr9 - 123373775 123373775 123373775 TTCGCAGCGCGGGCCTTCCCACCCCGGGCCGCAGGCGCAGGCAAAGGCGTCGAAGAGGTCACGGC TTCGCAGCGCGGGCCTTCCCACCCCGGGCCGCCGGCGCAGGCAAAGGCGTCGAAGAGGTCACGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123373725..123373816 26863196 MeRIP-seq:(Medium) rs1425817084 Functional Loss SNV dbSNP153 33..33 33 - - - 107045 RMVar_ID_107045 Human_SNP_ID_414618723 m1A Human chr9 - 123373775 123373775 123373775 TTCGCAGCGCGGGCCTTCCCACCCCGGGCCGCAGGCGCAGGCAAAGGCGTCGAAGAGGTCACGGC TTCGCAGCGCGGGCCTTCCCACCCCGGGCCGCGGGCGCAGGCAAAGGCGTCGAAGAGGTCACGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123373725..123373816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 107046 RMVar_ID_107046 Human_SNP_ID_414621750 m1A Human chr9 - 123381781 123381781 123381781 TCAGCCCAACCTCTCCGCCCTCTCCATGCCCAACCTCTTTGGCCAGATGCCCATGGGCACCCACA TCAGCCCAACCTCTCCGCCCTCTCCATGCCCAGCCTCTTTGGCCAGATGCCCATGGGCACCCACA T C DENND1A Ensembl:ENSG00000119522 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:123381735..123381813 26863196 MeRIP-seq:(Medium) rs1430900865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135287,Human_RBP_ID_17323614,Human_RBP_ID_18963043 107047 RMVar_ID_107047 Human_SNP_ID_414658382 m1A Human chr9 - 123527082 123527082 123527082 AGTGAATAGAAAAGAGAGAGAAAAGTAAAACAAGACCAACCCAGGTAACTGGGTGAGGCTATTCC AGTGAATAGAAAAGAGAGAGAAAAGTAAAACAGGACCAACCCAGGTAACTGGGTGAGGCTATTCC T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:123527077..123527256 26863196 MeRIP-seq:(Medium) rs919950898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104643,RMVar_hsa_circ_259371,RMVar_hsa_circ_365929,RMVar_hsa_circ_103766,RMVar_hsa_circ_259377,RMVar_hsa_circ_349212,RMVar_hsa_circ_313042,RMVar_hsa_circ_59256,RMVar_hsa_circ_72523,RMVar_hsa_circ_115401,RMVar_hsa_circ_29186,RMVar_hsa_circ_259378,RMVar_hsa_circ_259382,RMVar_hsa_circ_86090,RMVar_hsa_circ_110671,RMVar_hsa_circ_259384,RMVar_hsa_circ_259383,RMVar_hsa_circ_124091,RMVar_hsa_circ_28127,RMVar_hsa_circ_116681,RMVar_hsa_circ_259387,RMVar_hsa_circ_259389,RMVar_hsa_circ_76560,RMVar_hsa_circ_259390 107048 RMVar_ID_107048 Human_SNP_ID_414658391 m1A Human chr9 + 123527134 123527134 123527134 TTTTCTATTCACTCAAATCCTAAGCCCTGTGGATCCTATCCCTTCTCATTTCCCAAGCCCATCCA TTTTCTATTCACTCAAATCCTAAGCCCTGTGGTTCCTATCCCTTCTCATTTCCCAAGCCCATCCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr9:123527095..123527293;chr9:123527094..123527235 26863196 MeRIP-seq:(Medium) rs370833011 Functional Loss SNV dbSNP153 33..33 33 - - - 107049 RMVar_ID_107049 Human_SNP_ID_414720379 m1A Human chr9 + 123792621 123792621 123792621 GGTCACTGTAGTCCTCCGGGAATTGCCTCTGCACCTCAGGATCTGTAAATAATTGACAGATAATA GGTCACTGTAGTCCTCCGGGAATTGCCTCTGCGCCTCAGGATCTGTAAATAATTGACAGATAATA A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:123769549..123798302 26863196 MeRIP-seq:(Medium) rs1282830922 Functional Loss SNV dbSNP153 33..33 33 - - - 107050 RMVar_ID_107050 Human_SNP_ID_414722536 m1A Human chr9 - 123802447 123802447 123802447 CAATGCAGTATGATCCCCAAGAGTCAAGGATGAGGAATAACCCTGGAATTAGTAGGTGACAACAA CAATGCAGTATGATCCCCAAGAGTCAAGGATGGGGAATAACCCTGGAATTAGTAGGTGACAACAA T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123802444..123802584 26863196 MeRIP-seq:(Medium) rs1319207896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16563304 RMVar_hsa_circ_365929,RMVar_hsa_circ_313042,RMVar_hsa_circ_259378,RMVar_hsa_circ_110671,RMVar_hsa_circ_259384,RMVar_hsa_circ_116681,RMVar_hsa_circ_259389,RMVar_hsa_circ_76560,RMVar_hsa_circ_259390,RMVar_hsa_circ_276342,RMVar_hsa_circ_110084,RMVar_hsa_circ_259391,RMVar_hsa_circ_282912,RMVar_hsa_circ_259401,RMVar_hsa_circ_111189,RMVar_hsa_circ_313405,RMVar_hsa_circ_259409,RMVar_hsa_circ_259403,RMVar_hsa_circ_259402,RMVar_hsa_circ_274318,RMVar_hsa_circ_259421,RMVar_hsa_circ_297289,RMVar_hsa_circ_289634,RMVar_hsa_circ_113658,RMVar_hsa_circ_274725,RMVar_hsa_circ_259426,RMVar_hsa_circ_277639,RMVar_hsa_circ_259432,RMVar_hsa_circ_259429,RMVar_hsa_circ_259430,RMVar_hsa_circ_291551,RMVar_hsa_circ_259433,RMVar_hsa_circ_276881 107051 RMVar_ID_107051 Human_SNP_ID_414722538 m1A Human chr9 - 123802461 123802461 123802461 GTTAGAGTGAGTGGCAATGCAGTATGATCCCCAAGAGTCAAGGATGAGGAATAACCCTGGAATTA GTTAGAGTGAGTGGCAATGCAGTATGATCCCCTAGAGTCAAGGATGAGGAATAACCCTGGAATTA T A DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:123802460..123802594 26863196 MeRIP-seq:(Medium) rs1390582584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365929,RMVar_hsa_circ_313042,RMVar_hsa_circ_259378,RMVar_hsa_circ_110671,RMVar_hsa_circ_259384,RMVar_hsa_circ_116681,RMVar_hsa_circ_259389,RMVar_hsa_circ_76560,RMVar_hsa_circ_259390,RMVar_hsa_circ_276342,RMVar_hsa_circ_110084,RMVar_hsa_circ_259391,RMVar_hsa_circ_282912,RMVar_hsa_circ_259401,RMVar_hsa_circ_111189,RMVar_hsa_circ_313405,RMVar_hsa_circ_259409,RMVar_hsa_circ_259403,RMVar_hsa_circ_259402,RMVar_hsa_circ_274318,RMVar_hsa_circ_259421,RMVar_hsa_circ_297289,RMVar_hsa_circ_289634,RMVar_hsa_circ_113658,RMVar_hsa_circ_274725,RMVar_hsa_circ_259426,RMVar_hsa_circ_277639,RMVar_hsa_circ_259432,RMVar_hsa_circ_259429,RMVar_hsa_circ_259430,RMVar_hsa_circ_291551,RMVar_hsa_circ_259433,RMVar_hsa_circ_276881 107052 RMVar_ID_107052 Human_SNP_ID_414751735 m1A Human chr9 + 123929467 123929464 123929467 TAAGAACCTCACGCGACTTCTGTGGGGGCCGCAGGCCTCAAGCGGCCAGGCTGCAACCTCTCCGG TAAGAACCTCACGCGACTTCTGTGGGGGCC___GGCCTCAAGCGGCCAGGCTGCAACCTCTCCGG CGCA C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:123929458..123929587 26863196 MeRIP-seq:(Medium) rs965464485 Functional Loss DEL dbSNP153 31..33 33 - - - 107053 RMVar_ID_107053 Human_SNP_ID_414751898 m1A Human chr9 - 123929954 123929954 123929954 GAGGGAGGCCGGTCGGCCGCGGGCGGGCGGGCAGCGCAGCGCCGAGCGGGGCCCGCGGGCCCATG GAGGGAGGCCGGTCGGCCGCGGGCGGGCGGGCGGCGCAGCGCCGAGCGGGGCCCGCGGGCCCATG T C DENND1A Ensembl:ENSG00000119522 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:123929866..123930095 26863196 MeRIP-seq:(Medium) rs999480570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255869,Human_RBP_ID_847615,Human_RBP_ID_963737,Human_RBP_ID_1070501,Human_RBP_ID_3906359,Human_RBP_ID_3974771,Human_RBP_ID_5329603,Human_RBP_ID_8160048,Human_RBP_ID_9339039,Human_RBP_ID_9442740,Human_RBP_ID_18427213,Human_RBP_ID_18962266,Human_RBP_ID_19025552 Human_Splice_Rec_1078811,Human_Splice_Rec_1078853,Human_Splice_Rec_1078961 RMVar_hsa_circ_110084,RMVar_hsa_circ_259391,RMVar_hsa_circ_111189,RMVar_hsa_circ_259402,RMVar_hsa_circ_113658,RMVar_hsa_circ_259430 107054 RMVar_ID_107054 Human_SNP_ID_414751911 m1A Human chr9 - 123929987 123929987 123929987 GAGGGAAGGGAGGAAGGGGCGGGGAGAGCGCCAGAGGGAGGCCGGTCGGCCGCGGGCGGGCGGGC GAGGGAAGGGAGGAAGGGGCGGGGAGAGCGCCTGAGGGAGGCCGGTCGGCCGCGGGCGGGCGGGC T A DENND1A Ensembl:ENSG00000119522 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:123929345..123930175 26863196 MeRIP-seq:(Medium) rs1452854045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847615,Human_RBP_ID_963737,Human_RBP_ID_3906360,Human_RBP_ID_3974771,Human_RBP_ID_5329603,Human_RBP_ID_8160048,Human_RBP_ID_9339039,Human_RBP_ID_18427213,Human_RBP_ID_18962266,Human_RBP_ID_19025552 Human_Splice_Rec_1078811,Human_Splice_Rec_1078853,Human_Splice_Rec_1078961 RMVar_hsa_circ_110084,RMVar_hsa_circ_259391,RMVar_hsa_circ_111189,RMVar_hsa_circ_259402,RMVar_hsa_circ_113658,RMVar_hsa_circ_259430 107055 RMVar_ID_107055 Human_SNP_ID_414751947 m1A Human chr9 - 123930084 123930084 123930084 GCGACCATGGCGTTCGCCGGGCTGGAGCGAGTACATTAACCCCTGGAGGCGGCGGCGGCGGCGAG GCGACCATGGCGTTCGCCGGGCTGGAGCGAGTGCATTAACCCCTGGAGGCGGCGGCGGCGGCGAG T C DENND1A Ensembl:ENSG00000119522 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:123929887..123930118 26863196 MeRIP-seq:(Medium) rs910352226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110084,RMVar_hsa_circ_259391,RMVar_hsa_circ_111189,RMVar_hsa_circ_259402,RMVar_hsa_circ_113658,RMVar_hsa_circ_259430 107056 RMVar_ID_107056 Human_SNP_ID_414770120 m1A Human chr9 - 124000086 124000086 124000086 CCAGCGGGGGTGAGGGGGCCGTTGGCAGCCCCAGGGCCCTCGGGCGGGCCGGGCCGAGCCGGAGG CCAGCGGGGGTGAGGGGGCCGTTGGCAGCCCCGGGGCCCTCGGGCGGGCCGGGCCGAGCCGGAGG T C RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:123999920..124000182 26863410 MeRIP-seq:(Medium) rs1301555694 Functional Loss SNV dbSNP153 33..33 33 - - - 107057 RMVar_ID_107057 Human_SNP_ID_414773166 m1A Human chr9 + 124011829 124011829 124011829 AGGCTTCGGAGAAACCCCTACTCCAGTCGCCGACTCAGCGCCCAAGAGGGTCGCCTTGGGCTGGG AGGCTTCGGAGAAACCCCTACTCCAGTCGCCGGCTCAGCGCCCAAGAGGGTCGCCTTGGGCTGGG A G LHX2 Ensembl:ENSG00000106689 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:124011779..124011950 26863196 MeRIP-seq:(Medium) rs1233091123 Functional Loss SNV dbSNP153 33..33 33 - - - 107058 RMVar_ID_107058 Human_SNP_ID_414848033 m1A Human chr9 - 124294770 124294770 124294770 CCTGAACCTGCCAATCTCTCCTGAAACTCCACAGCAAAAGGTCCGCACACCGGAGCAAGCCATTC CCTGAACCTGCCAATCTCTCCTGAAACTCCACGGCAAAAGGTCCGCACACCGGAGCAAGCCATTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:124294768..124295003 26863196 MeRIP-seq:(Medium) rs1444711947 Functional Loss SNV dbSNP153 33..33 33 - - - 107059 RMVar_ID_107059 Human_SNP_ID_414850880 m1A Human chr9 - 124305997 124305997 124305997 CACCAGTGATCTATCTAGAACCCAACCCAAGTACCCCCTTGCCACCTGAAAACCCATAATGGGCT CACCAGTGATCTATCTAGAACCCAACCCAAGTTCCCCCTTGCCACCTGAAAACCCATAATGGGCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:124305992..124306126 26863196 MeRIP-seq:(Medium) rs79188548 Functional Loss SNV dbSNP153 33..33 33 - - - 107060 RMVar_ID_107060 Human_SNP_ID_414862153 m1A Human chr9 - 124347730 124347728 124347731 CAGGGAGAAGAGATTCATCTTATCTCCATAGAAGGGGCTCTGGAGGGCTGCCATCTGCAAGGGAC CAGGGAGAAGAGATTCATCTTATCTCCATAG___GGGCTCTGGAGGGCTGCCATCTGCAAGGGAC CCTT C RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:124347711..124347811 32194978 MeRIP-seq:(Medium) rs1156477599 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_16565155 107061 RMVar_ID_107061 Human_SNP_ID_414875752 m1A Human chr9 + 124405267 124405267 124405267 TAAGAGAAAACAGACCAGCTCTTCAAGAGACCATCGTGGTAAGTAAGAGTACTCTTAAACATCAG TAAGAGAAAACAGACCAGCTCTTCAAGAGACCGTCGTGGTAAGTAAGAGTACTCTTAAACATCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124405264..124405479 26863196 MeRIP-seq:(Medium) rs144936453 Functional Loss SNV dbSNP153 33..33 33 - - - 107062 RMVar_ID_107062 Human_SNP_ID_414877864 m1A Human chr9 - 124414004 124414004 124414004 AAAATTGTTTAAAAACTTTTTTTTTTAATAGGATGGCATAGTTCTTGGAGCAGATACAAGAGCAA AAAATTGTTTAAAAACTTTTTTTTTTAATAGGTTGGCATAGTTCTTGGAGCAGATACAAGAGCAA T A PSMB7 Ensembl:ENSG00000136930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124413956..124414061 26863196 MeRIP-seq:(Medium) rs1389185264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711447,Human_RBP_ID_16566714,Human_RBP_ID_19024310,Human_RBP_ID_22467400,Human_RBP_ID_24284672 Human_Splice_Rec_1079316,Human_Splice_Rec_1079317,Human_Splice_Rec_1079330,Human_Splice_Rec_1079331,Human_Splice_Rec_1079348,Human_Splice_Rec_1079349,Human_Splice_Rec_1079358,Human_Splice_Rec_1079359 RMVar_hsa_circ_115570,RMVar_hsa_circ_19035,RMVar_hsa_circ_259459,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52664,RMVar_hsa_circ_333929,RMVar_hsa_circ_259463 107063 RMVar_ID_107063 Human_SNP_ID_414877865 m1A Human chr9 - 124414004 124414004 124414004 AAAATTGTTTAAAAACTTTTTTTTTTAATAGGATGGCATAGTTCTTGGAGCAGATACAAGAGCAA AAAATTGTTTAAAAACTTTTTTTTTTAATAGGGTGGCATAGTTCTTGGAGCAGATACAAGAGCAA T C PSMB7 Ensembl:ENSG00000136930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124413956..124414061 26863196 MeRIP-seq:(Medium) rs1389185264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711447,Human_RBP_ID_16566714,Human_RBP_ID_19024310,Human_RBP_ID_22467400,Human_RBP_ID_24284672 Human_Splice_Rec_1079316,Human_Splice_Rec_1079317,Human_Splice_Rec_1079330,Human_Splice_Rec_1079331,Human_Splice_Rec_1079348,Human_Splice_Rec_1079349,Human_Splice_Rec_1079358,Human_Splice_Rec_1079359 RMVar_hsa_circ_115570,RMVar_hsa_circ_19035,RMVar_hsa_circ_259459,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52664,RMVar_hsa_circ_333929,RMVar_hsa_circ_259463 107064 RMVar_ID_107064 Human_SNP_ID_414878141 m1A Human chr9 - 124414894 124414894 124414894 CTTGGAAGCCGATTTTGCAAAGAGGGGATACAAGCTTCCAAAGGTCCGGAAAACTGGCACGACCA CTTGGAAGCCGATTTTGCAAAGAGGGGATACAGGCTTCCAAAGGTCCGGAAAACTGGCACGACCA T C PSMB7 Ensembl:ENSG00000136930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124414789..124414972 26863196 MeRIP-seq:(Medium) rs1465190532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91215,Human_RBP_ID_5008983,Human_RBP_ID_18140621,Human_RBP_ID_22467401 Human_Splice_Rec_1079314,Human_Splice_Rec_1079315,Human_Splice_Rec_1079328,Human_Splice_Rec_1079329,Human_Splice_Rec_1079346,Human_Splice_Rec_1079347,Human_Splice_Rec_1079357 RMVar_hsa_circ_19035,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52664,RMVar_hsa_circ_333929,RMVar_hsa_circ_259465,RMVar_hsa_circ_259463,RMVar_hsa_circ_92482 107065 RMVar_ID_107065 Human_SNP_ID_414878328 m1A Human chr9 + 124415413 124415413 124415413 AGAGAAGCCTCCAACTGGTGGAGCATACACCGACACAGCCGCCATCTTCCCAAGAAAGCAGTTCC AGAGAAGCCTCCAACTGGTGGAGCATACACCGGCACAGCCGCCATCTTCCCAAGAAAGCAGTTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:124415299..124415450;chr9:124415250..124415450;chr9:124415284..124415450 26863196 MeRIP-seq:(Medium) rs1032457936 Functional Loss SNV dbSNP153 33..33 33 - - - 107066 RMVar_ID_107066 Human_SNP_ID_414887444 m1A Human chr9 - 124450608 124450608 124450608 GGCCCGAGAGGGAGATGCGAAGTTTGCCCACCACTGCGCGTCCCTCCTCCGCGAGGCGCCAATGG GGCCCGAGAGGGAGATGCGAAGTTTGCCCACCGCTGCGCGTCCCTCCTCCGCGAGGCGCCAATGG T C HSALNG0074337 RNACentral:URS0000EB6617 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124450564..124450727 26863196 MeRIP-seq:(Medium) rs548940180 Functional Loss SNV dbSNP153 33..33 33 - - - 107067 RMVar_ID_107067 Human_SNP_ID_414909859 m1A Human chr9 - 124532133 124532133 124532133 AGACAGAGAAATGAGGGGAGAATTGACTAGAGAGAAAGATACAGGCAAGACAGGTCATGAAGGTG AGACAGAGAAATGAGGGGAGAATTGACTAGAGGGAAAGATACAGGCAAGACAGGTCATGAAGGTG T C NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:124532084..124532158 26863196 MeRIP-seq:(Medium) rs1392232917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_704,RMVar_hsa_circ_13428,RMVar_hsa_circ_337985,RMVar_hsa_circ_371421,RMVar_hsa_circ_303455,RMVar_hsa_circ_64018,RMVar_hsa_circ_259467,RMVar_hsa_circ_306401,RMVar_hsa_circ_12542 107068 RMVar_ID_107068 Human_SNP_ID_414945991 m1A Human chr9 - 124683183 124683183 124683183 CTTTTCTTTTCTGTCTTGGAGGGTCTCACTCTATGCCCCAGGCTGGAGTGTAGTGGCGTGATCCC CTTTTCTTTTCTGTCTTGGAGGGTCTCACTCTGTGCCCCAGGCTGGAGTGTAGTGGCGTGATCCC T C NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:124683180..124683279 26863196 MeRIP-seq:(Medium) rs866104631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18963061,Human_RBP_ID_21684236 RMVar_hsa_circ_259471,RMVar_hsa_circ_105444 107069 RMVar_ID_107069 Human_SNP_ID_414966837 m1A Human chr9 + 124770274 124770265 124770275 GCCTGGCGGAGAGGGGAGCTGAGCAGGGGCGGAGACCGGCCAGAGCGCGCGGGGCGTTGAGGAAG GCCTGGCGGAGAGGGGAGCTGAGC__________ACCGGCCAGAGCGCGCGGGGCGTTGAGGAAG CAGGGGCGGAG C AL354928.1 Ensembl:ENSG00000236643 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124770263..124770339 26863196 MeRIP-seq:(Medium) rs1191519556 Functional Loss DEL dbSNP153 25..34 33 - - - Human_Splice_Rec_1079597 107070 RMVar_ID_107070 Human_SNP_ID_414967311 m1A Human chr9 - 124771278 124771278 124771278 GTGCTGAGGGGGCGCGGCGCGGAGGGGCGCGGAGCGGCGCGGAGCCGGGCGGCTCGGGGCCCAGA GTGCTGAGGGGGCGCGGCGCGGAGGGGCGCGGGGCGGCGCGGAGCCGGGCGGCTCGGGGCCCAGA T C NR6A1 Ensembl:ENSG00000148200 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:124733340..124771303;chr9:124733340..124771297 26863196 MeRIP-seq:(Medium) rs1428879694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5009017,Human_RBP_ID_9408499,Human_RBP_ID_18427214 107071 RMVar_ID_107071 Human_SNP_ID_414968937 m1A Human chr9 + 124777455 124777455 124777455 CTGGGGTGCGGCCCGGGAGGGAGCCCGGGGCCAGGGCGGAGGAGCCGGGAGCTGAGAGACCGAAC CTGGGGTGCGGCCCGGGAGGGAGCCCGGGGCCGGGGCGGAGGAGCCGGGAGCTGAGAGACCGAAC A G OLFML2A Ensembl:ENSG00000185585 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:124777445..124777574 26863196 MeRIP-seq:(Medium) rs918828468 Functional Loss SNV dbSNP153 33..33 33 - - - 107072 RMVar_ID_107072 Human_SNP_ID_414971416 m1A Human chr9 - 124787146 124787146 124787146 GTTGAGAGAGGAGGGAGGTGCGGTACAGGAGCAGCGGCAGTCAGTGCCCGAGCTCACAGTCTCCA GTTGAGAGAGGAGGGAGGTGCGGTACAGGAGCGGCGGCAGTCAGTGCCCGAGCTCACAGTCTCCA T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:124787097..124787170 26863196 MeRIP-seq:(Medium) rs1012909616 Functional Loss SNV dbSNP153 33..33 33 - - - 107073 RMVar_ID_107073 Human_SNP_ID_414975590 m1A Human chr9 + 124804281 124804281 124804281 CCTGCCACCACCACCACCGCCACCACCACCCCAACCCCCACCACCAGTCTCCTGCCCACCGAGCC CCTGCCACCACCACCACCGCCACCACCACCCCCACCCCCACCACCAGTCTCCTGCCCACCGAGCC A C OLFML2A Ensembl:ENSG00000185585 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124804232..124804395 26863196 MeRIP-seq:(Medium) rs879618683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1079611,Human_Splice_Rec_1079627 RMVar_hsa_circ_41060,RMVar_hsa_circ_49137,RMVar_hsa_circ_43171,RMVar_hsa_circ_341083 107074 RMVar_ID_107074 Human_SNP_ID_414991564 m1A Human chr9 + 124858023 124858023 124858023 TCCTCGTGCTTGTTGAGCCGGCGGCGCATGGCACGTGTCTTCTTAGGCCGCAGGTCCAGGGGCTT TCCTCGTGCTTGTTGAGCCGGCGGCGCATGGCGCGTGTCTTCTTAGGCCGCAGGTCCAGGGGCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:124857898..124858075;chr9:124857876..124858286;chr9:124857941..124858075 26863196 MeRIP-seq:(Medium) rs370854864 Functional Loss SNV dbSNP153 33..33 33 - - - 107075 RMVar_ID_107075 Human_SNP_ID_414992222 m1A Human chr9 - 124860245 124860245 124860245 CTCTGTTTTGTAGCCGAGTCGTCCGGAAATCCATTGCCCGTGTTCTCACAGTTATTAACCAGACT CTCTGTTTTGTAGCCGAGTCGTCCGGAAATCCGTTGCCCGTGTTCTCACAGTTATTAACCAGACT T C RPL35 Ensembl:ENSG00000136942 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:124858532..124860991 26863196 MeRIP-seq:(Medium) rs1340035392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91249,Human_RBP_ID_711519,Human_RBP_ID_1057869,Human_RBP_ID_1402445,Human_RBP_ID_1701906,Human_RBP_ID_2060473,Human_RBP_ID_3187793,Human_RBP_ID_3893068,Human_RBP_ID_8696386,Human_RBP_ID_9232701,Human_RBP_ID_16571034,Human_RBP_ID_17321119,Human_RBP_ID_17435467,Human_RBP_ID_17548376,Human_RBP_ID_17666562,Human_RBP_ID_18129442,Human_RBP_ID_18903443,Human_RBP_ID_22335073,Human_RBP_ID_22517713,Human_RBP_ID_23200013,Human_RBP_ID_26834232,Human_RBP_ID_27130046,Human_RBP_ID_27541913,Human_RBP_ID_27782980 Human_Splice_Rec_1079680,Human_Splice_Rec_1079681,Human_Splice_Rec_1079688,Human_Splice_Rec_1079689,Human_Splice_Rec_1079694,Human_Splice_Rec_1079695,Human_Splice_Rec_1079700,Human_Splice_Rec_1079701,Human_Splice_Rec_1079706,Human_Splice_Rec_1079707 Human_miRNA_ID_2378024,Human_miRNA_ID_2672575,Human_miRNA_ID_3093096 RMVar_hsa_circ_124949,RMVar_hsa_circ_122879,RMVar_hsa_circ_259478,RMVar_hsa_circ_259480,RMVar_hsa_circ_89612,RMVar_hsa_circ_259479,RMVar_hsa_circ_367095 107076 RMVar_ID_107076 Human_SNP_ID_414992625 m1A Human chr9 - 124861521 124861521 124861521 CAAGATCAAGGCTCGAGATCTTCGCGGGAAGAAGAAGGAGGAGCTGCTGAAACAGCTGGACGACC CAAGATCAAGGCTCGAGATCTTCGCGGGAAGAGGAAGGAGGAGCTGCTGAAACAGCTGGACGACC T C RPL35 Ensembl:ENSG00000136942 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr9:124861380..124861600;chr9:124861358..124861625 26863410 MeRIP-seq:(Medium) rs758233686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91250,Human_RBP_ID_255985,Human_RBP_ID_711526,Human_RBP_ID_797485,Human_RBP_ID_846582,Human_RBP_ID_966033,Human_RBP_ID_1701920,Human_RBP_ID_2060475,Human_RBP_ID_3187800,Human_RBP_ID_3893070,Human_RBP_ID_5036391,Human_RBP_ID_5123999,Human_RBP_ID_7897124,Human_RBP_ID_8275104,Human_RBP_ID_8696394,Human_RBP_ID_9232702,Human_RBP_ID_9407376,Human_RBP_ID_18541914,Human_RBP_ID_18903448,Human_RBP_ID_22118839,Human_RBP_ID_22517716,Human_RBP_ID_22837644,Human_RBP_ID_23089703,Human_RBP_ID_24285155,Human_RBP_ID_26202399,Human_RBP_ID_26360468,Human_RBP_ID_26834240,Human_RBP_ID_27130054,Human_RBP_ID_27370063,Human_RBP_ID_27833385 Human_Splice_Rec_1079678,Human_Splice_Rec_1079686,Human_Splice_Rec_1079698,Human_Splice_Rec_1079704,Human_Splice_Rec_1079710 RMVar_hsa_circ_124949,RMVar_hsa_circ_122879,RMVar_hsa_circ_259480,RMVar_hsa_circ_259479,RMVar_hsa_circ_367095 107077 RMVar_ID_107077 Human_SNP_ID_414992637 m1A Human chr9 - 124861557 124861557 124861557 GGCCTGGCTGAGGCACACTCTCTCTTGCGCGCAGGCCAAGATCAAGGCTCGAGATCTTCGCGGGA GGCCTGGCTGAGGCACACTCTCTCTTGCGCGCGGGCCAAGATCAAGGCTCGAGATCTTCGCGGGA T C RPL35 Ensembl:ENSG00000136942 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr9:124861526..124861575;chr9:124861551..124861575 26863196 MeRIP-seq:(Medium) rs1329982012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91250,Human_RBP_ID_22837645,Human_RBP_ID_26202400,Human_RBP_ID_26796520 RMVar_hsa_circ_122879,RMVar_hsa_circ_259480 107078 RMVar_ID_107078 Human_SNP_ID_414992975 m1A Human chr9 - 124862251 124862247 124862251 GTTTCCCGAAGGAATGAATGAACGAATGACTGAATGGACGAATTTGAGTCCTCCGTGTGCCATCT GTTTCCCGAAGGAATGAATGAACGAATGACTG____GACGAATTTGAGTCCTCCGTGTGCCATCT CCATT C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:124862203..124862347 26863196 MeRIP-seq:(Medium) rs766836634 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_24285157 107079 RMVar_ID_107079 Human_SNP_ID_414994881 m1A Human chr9 + 124869236 124869236 124869236 CGCCCCCGAGCAGGAGCCGGTGCGAGCGGAGCAGAGCCGAGGTCGGGCCGCGAGCGGAGCCGGCT CGCCCCCGAGCAGGAGCCGGTGCGAGCGGAGCCGAGCCGAGGTCGGGCCGCGAGCGGAGCCGGCT A C ARPC5L Ensembl:ENSG00000136950 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:124869191..124869576 26863196 MeRIP-seq:(Medium) rs1487799713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255987,Human_RBP_ID_5009051,Human_RBP_ID_8944642 Human_miRNA_ID_2395219,Human_miRNA_ID_3068958 RMVar_hsa_circ_117440,RMVar_hsa_circ_259481 107080 RMVar_ID_107080 Human_SNP_ID_414996012 m1A Human chr9 + 124873660 124873660 124873660 TGAGCTTGTTCATGACGGCATGGATGTGCTTGAGCCTAGCTATCCTTAACTGGTGGTGATGCACA TGAGCTTGTTCATGACGGCATGGATGTGCTTGCGCCTAGCTATCCTTAACTGGTGGTGATGCACA A C ARPC5L Ensembl:ENSG00000136950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:124873659..124875018 32194978 MeRIP-seq:(Medium) rs757489021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117440,RMVar_hsa_circ_259481 107081 RMVar_ID_107081 Human_SNP_ID_414996013 m1A Human chr9 + 124873660 124873660 124873660 TGAGCTTGTTCATGACGGCATGGATGTGCTTGAGCCTAGCTATCCTTAACTGGTGGTGATGCACA TGAGCTTGTTCATGACGGCATGGATGTGCTTGGGCCTAGCTATCCTTAACTGGTGGTGATGCACA A G ARPC5L Ensembl:ENSG00000136950 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:124873659..124875018 32194978 MeRIP-seq:(Medium) rs757489021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117440,RMVar_hsa_circ_259481 107082 RMVar_ID_107082 Human_SNP_ID_414996022 m1A Human chr9 - 124873678 124873678 124873678 TGCCCGAAGCATGTCCCCTGTGCATCACCACCAGTTAAGGATAGCTAGGCTCAAGCACATCCATG TGCCCGAAGCATGTCCCCTGTGCATCACCACCGGTTAAGGATAGCTAGGCTCAAGCACATCCATG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:124873676..124873775 26863196 MeRIP-seq:(Medium) rs775426914 Functional Loss SNV dbSNP153 33..33 33 - - - 107083 RMVar_ID_107083 Human_SNP_ID_414996052 m1A Human chr9 + 124873748 124873748 124873748 TGCAGCCTTGCGGAACTCTCCCGTCAACACCAAGAATCAAGCTGTGAAGGTAAAGGGGTGGCGCT TGCAGCCTTGCGGAACTCTCCCGTCAACACCAGGAATCAAGCTGTGAAGGTAAAGGGGTGGCGCT A G ARPC5L Ensembl:ENSG00000136950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124873646..124873787 26863196 MeRIP-seq:(Medium) rs758502389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711535,Human_RBP_ID_1701929,Human_RBP_ID_2060477,Human_RBP_ID_19145760,Human_RBP_ID_27541917 Human_Splice_Rec_1079713,Human_Splice_Rec_1079717,Human_Splice_Rec_1079721 RMVar_hsa_circ_117440,RMVar_hsa_circ_259481 107084 RMVar_ID_107084 Human_SNP_ID_414996405 m1A Human chr9 + 124875036 124875036 124875036 GCTCACAAACTTCAAGAGCAGTGAGATTGAGCAGGCTGTGCAGTCACTGGACAGAAACGGCGTTG GCTCACAAACTTCAAGAGCAGTGAGATTGAGCGGGCTGTGCAGTCACTGGACAGAAACGGCGTTG A G ARPC5L Ensembl:ENSG00000136950 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:124874917..124875075 26863196 MeRIP-seq:(Medium) rs763224383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711539,Human_RBP_ID_1701932,Human_RBP_ID_2060478,Human_RBP_ID_5009064,Human_RBP_ID_5124513,Human_RBP_ID_5633593,Human_RBP_ID_7897148,Human_RBP_ID_8925272,Human_RBP_ID_16571237,Human_RBP_ID_18140625,Human_RBP_ID_18903455,Human_RBP_ID_24285182 Human_Splice_Rec_1079714,Human_Splice_Rec_1079718,Human_Splice_Rec_1079722 Human_miRNA_ID_2037139,Human_miRNA_ID_2347841 RMVar_hsa_circ_104433,RMVar_hsa_circ_117440,RMVar_hsa_circ_259481,RMVar_hsa_circ_259482 107085 RMVar_ID_107085 Human_SNP_ID_414997043 m1A Human chr9 + 124877257 124877257 124877257 CACTGGGGGAGGGATGGTTTGGGCAGGTGCAGATCCAAGGGCTGTGGTAAACGGGAGAGCTTGTG CACTGGGGGAGGGATGGTTTGGGCAGGTGCAGTTCCAAGGGCTGTGGTAAACGGGAGAGCTTGTG A T ARPC5L Ensembl:ENSG00000136950 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:124877089..124877288 32194978 MeRIP-seq:(Medium) rs576135544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711550,Human_RBP_ID_846764,Human_RBP_ID_5037072,Human_RBP_ID_5124000,Human_RBP_ID_5154457,Human_RBP_ID_7897162,Human_RBP_ID_9355053,Human_RBP_ID_17666564,Human_RBP_ID_24285194,Human_RBP_ID_26560708 Human_miRNA_ID_2001675,Human_miRNA_ID_2003059,Human_miRNA_ID_2055632 RMVar_hsa_circ_105489,RMVar_hsa_circ_104433,RMVar_hsa_circ_117440,RMVar_hsa_circ_259481,RMVar_hsa_circ_259482,RMVar_hsa_circ_259483 107086 RMVar_ID_107086 Human_SNP_ID_415006214 m1A Human chr9 - 124911952 124911952 124911952 TTGCAAGAGAAGGTTGCATCCTTGGAGAAGAGACTAGAACAGAACTTATCAGGAGAAGAACACTT TTGCAAGAGAAGGTTGCATCCTTGGAGAAGAGGCTAGAACAGAACTTATCAGGAGAAGAACACTT T C GOLGA1 Ensembl:ENSG00000136935 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:124911822..124912029 26863196 MeRIP-seq:(Medium) rs746121055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963765,Human_RBP_ID_9407384,Human_RBP_ID_16571306,Human_RBP_ID_24549644,Human_RBP_ID_26362069,Human_RBP_ID_27832689 Human_Splice_Rec_1079744,Human_Splice_Rec_1079745,Human_Splice_Rec_1079778,Human_Splice_Rec_1079779,Human_Splice_Rec_1079806,Human_Splice_Rec_1079807,Human_Splice_Rec_1079819 RMVar_hsa_circ_2049,RMVar_hsa_circ_89330,RMVar_hsa_circ_259485,RMVar_hsa_circ_259484,RMVar_hsa_circ_259486,RMVar_hsa_circ_72408,RMVar_hsa_circ_50603,RMVar_hsa_circ_99632,RMVar_hsa_circ_259488,RMVar_hsa_circ_259489,RMVar_hsa_circ_109956,RMVar_hsa_circ_304445,RMVar_hsa_circ_358528,RMVar_hsa_circ_259493,RMVar_hsa_circ_259491,RMVar_hsa_circ_267397,RMVar_hsa_circ_111604,RMVar_hsa_circ_9047,RMVar_hsa_circ_344722,RMVar_hsa_circ_367396,RMVar_hsa_circ_271054,RMVar_hsa_circ_259494,RMVar_hsa_circ_259495,RMVar_hsa_circ_46632 107087 RMVar_ID_107087 Human_SNP_ID_415063156 m1A Human chr9 - 125143058 125143058 125143058 GGGGTCGCCGGGCCCGGAGAGGCGGGGCGTGGAGGGGGCAGTGCACGGTCGGGAACGGGTGGGCA GGGGTCGCCGGGCCCGGAGAGGCGGGGCGTGGGGGGGGCAGTGCACGGTCGGGAACGGGTGGGCA T C SCAI Ensembl:ENSG00000173611 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125143051..125143267 26863196 MeRIP-seq:(Medium) rs976234954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92131,RMVar_hsa_circ_259541,RMVar_hsa_circ_96546,RMVar_hsa_circ_259549 107088 RMVar_ID_107088 Human_SNP_ID_415064531 m1A Human chr9 - 125148028 125148028 125148028 GCTCCTTACATAGTTTTTAATTATATAGCTATATGAAAGAGGTGGCTAAGACATTTGCTGCACAC GCTCCTTACATAGTTTTTAATTATATAGCTATGTGAAAGAGGTGGCTAAGACATTTGCTGCACAC T C PPP6C Ensembl:ENSG00000119414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1549314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3188015,Human_RBP_ID_24522203,Human_RBP_ID_26560724 GWAS_ID_14661,GWAS_ID_14662,GWAS_ID_14663,GWAS_ID_14664,GWAS_ID_14665,GWAS_ID_14666,GWAS_ID_14667,GWAS_ID_14668,GWAS_ID_14669,GWAS_ID_14670,GWAS_ID_14671,GWAS_ID_14672,GWAS_ID_14673,GWAS_ID_14674,GWAS_ID_14675,GWAS_ID_14676,GWAS_ID_14677,GWAS_ID_14678,GWAS_ID_14679,GWAS_ID_14680,GWAS_ID_14681,GWAS_ID_14682,GWAS_ID_14683,GWAS_ID_14684,GWAS_ID_14685,GWAS_ID_14686,GWAS_ID_14687,GWAS_ID_14688,GWAS_ID_14689,GWAS_ID_14690,GWAS_ID_14691,GWAS_ID_14692,GWAS_ID_14693,GWAS_ID_14694,GWAS_ID_14695,GWAS_ID_14696,GWAS_ID_14697,GWAS_ID_14698,GWAS_ID_14699,GWAS_ID_14700,GWAS_ID_14701,GWAS_ID_14702,GWAS_ID_14703,GWAS_ID_14704,GWAS_ID_14705,GWAS_ID_14706,GWAS_ID_14707,GWAS_ID_14708,GWAS_ID_14709,GWAS_ID_14710,GWAS_ID_14711,GWAS_ID_14712,GWAS_ID_14713,GWAS_ID_14714,GWAS_ID_14715,GWAS_ID_14716,GWAS_ID_14717,GWAS_ID_14718,GWAS_ID_14719,GWAS_ID_14720,GWAS_ID_14721,GWAS_ID_14722,GWAS_ID_14723,GWAS_ID_14724,GWAS_ID_14725 107089 RMVar_ID_107089 Human_SNP_ID_415064532 m1A Human chr9 - 125148028 125148028 125148028 GCTCCTTACATAGTTTTTAATTATATAGCTATATGAAAGAGGTGGCTAAGACATTTGCTGCACAC GCTCCTTACATAGTTTTTAATTATATAGCTATCTGAAAGAGGTGGCTAAGACATTTGCTGCACAC T G PPP6C Ensembl:ENSG00000119414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1549314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3188015,Human_RBP_ID_24522203,Human_RBP_ID_26560724 GWAS_ID_14661,GWAS_ID_14662,GWAS_ID_14663,GWAS_ID_14664,GWAS_ID_14665,GWAS_ID_14666,GWAS_ID_14667,GWAS_ID_14668,GWAS_ID_14669,GWAS_ID_14670,GWAS_ID_14671,GWAS_ID_14672,GWAS_ID_14673,GWAS_ID_14674,GWAS_ID_14675,GWAS_ID_14676,GWAS_ID_14677,GWAS_ID_14678,GWAS_ID_14679,GWAS_ID_14680,GWAS_ID_14681,GWAS_ID_14682,GWAS_ID_14683,GWAS_ID_14684,GWAS_ID_14685,GWAS_ID_14686,GWAS_ID_14687,GWAS_ID_14688,GWAS_ID_14689,GWAS_ID_14690,GWAS_ID_14691,GWAS_ID_14692,GWAS_ID_14693,GWAS_ID_14694,GWAS_ID_14695,GWAS_ID_14696,GWAS_ID_14697,GWAS_ID_14698,GWAS_ID_14699,GWAS_ID_14700,GWAS_ID_14701,GWAS_ID_14702,GWAS_ID_14703,GWAS_ID_14704,GWAS_ID_14705,GWAS_ID_14706,GWAS_ID_14707,GWAS_ID_14708,GWAS_ID_14709,GWAS_ID_14710,GWAS_ID_14711,GWAS_ID_14712,GWAS_ID_14713,GWAS_ID_14714,GWAS_ID_14715,GWAS_ID_14716,GWAS_ID_14717,GWAS_ID_14718,GWAS_ID_14719,GWAS_ID_14720,GWAS_ID_14721,GWAS_ID_14722,GWAS_ID_14723,GWAS_ID_14724,GWAS_ID_14725 107090 RMVar_ID_107090 Human_SNP_ID_415064973 m1A Human chr9 - 125149877 125149877 125149877 AACAACTTAAAACTCATCTGCAGAGCACATCAACTAGTGCACGAAGGCTATAAATTTATGTTTGA AACAACTTAAAACTCATCTGCAGAGCACATCAGCTAGTGCACGAAGGCTATAAATTTATGTTTGA T C PPP6C Ensembl:ENSG00000119414 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs200973884 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1057889,Human_RBP_ID_7897537,Human_RBP_ID_9232753,Human_RBP_ID_22335141,Human_RBP_ID_24285495,Human_RBP_ID_26833516,Human_RBP_ID_27541951 Human_Splice_Rec_1079972,Human_Splice_Rec_1079986,Human_Splice_Rec_1079996 107091 RMVar_ID_107091 Human_SNP_ID_415076208 m1A Human chr9 + 125189762 125189742 125189763 CAAGCCGCGGCAACAGCGGCGGCGGCGGCTGTAGCAGCGGCGGCGGCAGCGGCGGAGGCCGAAGC CAAGCCGCGGCAA_____________________CAGCGGCGGCGGCAGCGGCGGAGGCCGAAGC ACAGCGGCGGCGGCGGCTGTAG A L13712-001,lnc-RABEPK-3 RNACentral:URS0000334622,RNACentral:URS00008B2FB1 misc_RNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125189626..125189800 26863196 MeRIP-seq:(Medium) rs761898525 Functional Loss DEL dbSNP153 14..34 33 - - - 107092 RMVar_ID_107092 Human_SNP_ID_415076244 m1A Human chr9 - 125189759 125189759 125189759 TCGGCCTCCGCCGCTGCCGCCGCCGCTGCTACAGCCGCCGCCGCCGCTGTTGCCGCGGCTTGTTA TCGGCCTCCGCCGCTGCCGCCGCCGCTGCTACTGCCGCCGCCGCCGCTGTTGCCGCGGCTTGTTA T A PPP6C Ensembl:ENSG00000119414 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:125189626..125189800;chr9:125189626..125189879;chr9:125189676..125189800 26863196 MeRIP-seq:(Medium) rs771844666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5009191 107093 RMVar_ID_107093 Human_SNP_ID_415076245 m1A Human chr9 - 125189759 125189759 125189759 TCGGCCTCCGCCGCTGCCGCCGCCGCTGCTACAGCCGCCGCCGCCGCTGTTGCCGCGGCTTGTTA TCGGCCTCCGCCGCTGCCGCCGCCGCTGCTACGGCCGCCGCCGCCGCTGTTGCCGCGGCTTGTTA T C PPP6C Ensembl:ENSG00000119414 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:125189626..125189800;chr9:125189626..125189879;chr9:125189676..125189800 26863196 MeRIP-seq:(Medium) rs771844666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5009191 107094 RMVar_ID_107094 Human_SNP_ID_415079166 m1A Human chr9 - 125200579 125200579 125200579 CTCGCCCCTACCCTCCAGCCCCGGACTGCAATACCTGCGGCGACTTAGGCCAGTCGCGAGCCGTG CTCGCCCCTACCCTCCAGCCCCGGACTGCAATGCCTGCGGCGACTTAGGCCAGTCGCGAGCCGTG T C RF00017-4596,RF00017-4495,RF00017-4490 RNACentral:URS0000934741,RNACentral:URS0000923EDC,RNACentral:URS0000941A94 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125200569..125200736 26863196 MeRIP-seq:(Medium) rs376770742 Functional Loss SNV dbSNP153 33..33 33 - - - 107095 RMVar_ID_107095 Human_SNP_ID_415079184 m1A Human chr9 - 125200614 125200614 125200614 GCCCGAGACCGTGATAGACCCGGTATCCGGGGACCCTCGCCCCTACCCTCCAGCCCCGGACTGCA GCCCGAGACCGTGATAGACCCGGTATCCGGGGTCCCTCGCCCCTACCCTCCAGCCCCGGACTGCA T A RF00017-4596,RF00017-4495,RF00017-4490 RNACentral:URS0000934741,RNACentral:URS0000923EDC,RNACentral:URS0000941A94 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125200603..125200735 26863196 MeRIP-seq:(Medium) rs112568649 Functional Loss SNV dbSNP153 33..33 33 - - - 107096 RMVar_ID_107096 Human_SNP_ID_415080968 m1A Human chr9 - 125207605 125207605 125207605 CAACTGGGGGTAAATATGAACAGCTGTGGCCAACTCGAGCACAGGGGCTGTCTCCAGGGACAGTC CAACTGGGGGTAAATATGAACAGCTGTGGCCAGCTCGAGCACAGGGGCTGTCTCCAGGGACAGTC T C RF00017-4596,RF00017-4495,RF00017-4490 RNACentral:URS0000934741,RNACentral:URS0000923EDC,RNACentral:URS0000941A94 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:125203061..125220546 32194978 MeRIP-seq:(Medium) rs1352815186 Functional Loss SNV dbSNP153 33..33 33 - - - 107097 RMVar_ID_107097 Human_SNP_ID_415088972 m1A Human chr9 + 125236727 125236727 125236727 TTCTTCTTAGCTTTGAAGTCTTCAATGTCAGCATCTTGGTGGCTTTCCAGCCATTCAATCTTTTC TTCTTCTTAGCTTTGAAGTCTTCAATGTCAGCTTCTTGGTGGCTTTCCAGCCATTCAATCTTTTC A T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125236611..125236761 26863196 MeRIP-seq:(Medium) rs1005567551 Functional Loss SNV dbSNP153 33..33 33 - - - 107098 RMVar_ID_107098 Human_SNP_ID_415089017 m1A Human chr9 + 125236910 125236910 125236910 TCAATGCGCTCCTTGAGCTTTTTGTCTTCCTCAGCAAACTTCTCAGCATCATTAACCATCCTTTC TCAATGCGCTCCTTGAGCTTTTTGTCTTCCTCGGCAAACTTCTCAGCATCATTAACCATCCTTTC A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125236860..125236986 26863196 MeRIP-seq:(Medium) rs1315397534 Functional Loss SNV dbSNP153 33..33 33 - - - 107099 RMVar_ID_107099 Human_SNP_ID_415089448 m1A Human chr9 + 125238578 125238578 125238578 CAAGCTACTGAATCACTAAGAAAGATGCTGCGATGATGACCTACCTGTATCTTGATCACCAGAGA CAAGCTACTGAATCACTAAGAAAGATGCTGCGGTGATGACCTACCTGTATCTTGATCACCAGAGA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:125238576..125238650 32194978 MeRIP-seq:(Medium) rs1190132963 Functional Loss SNV dbSNP153 33..33 33 - - - 107100 RMVar_ID_107100 Human_SNP_ID_415089611 m1A Human chr9 - 125239117 125239116 125239117 TGGAACACTTCATCAAACTGTACAAAAAGAAGACGGGCAAAGATGTCAGGAAAGACAATAGAGCT TGGAACACTTCATCAAACTGTACAAAAAGAAG_CGGGCAAAGATGTCAGGAAAGACAATAGAGCT GT G HSPA5 Ensembl:ENSG00000044574 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:125239067..125239242 26863196 MeRIP-seq:(Medium) rs779155689 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_90120,Human_RBP_ID_3188168,Human_RBP_ID_5038790,Human_RBP_ID_5633606,Human_RBP_ID_27130160,Human_RBP_ID_27541993 Human_miRNA_ID_2721938 RMVar_hsa_circ_54579,RMVar_hsa_circ_115152,RMVar_hsa_circ_259568,RMVar_hsa_circ_63405,RMVar_hsa_circ_8260,RMVar_hsa_circ_55636,RMVar_hsa_circ_106240,RMVar_hsa_circ_259569 107101 RMVar_ID_107101 Human_SNP_ID_415089664 m1A Human chr9 - 125239385 125239385 125239385 AGTATGAAATTCAGGGATACGGCATATTTGCCAAATAGTGGAAATGTGAAGTACTGACAAAACTT AGTATGAAATTCAGGGATACGGCATATTTGCCGAATAGTGGAAATGTGAAGTACTGACAAAACTT T C HSPA5 Ensembl:ENSG00000044574 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125239383..125239483 26863196 MeRIP-seq:(Medium) rs1296865110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3188170,Human_RBP_ID_5407354,Human_RBP_ID_22368511,Human_RBP_ID_22690218,Human_RBP_ID_22747788 RMVar_hsa_circ_54579,RMVar_hsa_circ_115152,RMVar_hsa_circ_259568,RMVar_hsa_circ_55636,RMVar_hsa_circ_106240,RMVar_hsa_circ_259569 107102 RMVar_ID_107102 Human_SNP_ID_415090242 m1A Human chr9 - 125241293 125241293 125241293 ACAGACAGATTGACCTATTGGGGTGTTTCGCGAGTGTGAGAGGGAAGCGCCGCGGCCTGTATTTC ACAGACAGATTGACCTATTGGGGTGTTTCGCGGGTGTGAGAGGGAAGCGCCGCGGCCTGTATTTC T C HSPA5 Ensembl:ENSG00000044574 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125240990..125241350 26863196 MeRIP-seq:(Medium) rs1166000893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92238,Human_RBP_ID_711812,Human_RBP_ID_846483,Human_RBP_ID_1226037,Human_RBP_ID_1702055,Human_RBP_ID_3893278,Human_RBP_ID_5009347,Human_RBP_ID_8696556,Human_RBP_ID_9264664,Human_RBP_ID_9339051,Human_RBP_ID_17715865,Human_RBP_ID_18472789,Human_RBP_ID_22118855,Human_RBP_ID_22466205,Human_RBP_ID_24285635,Human_RBP_ID_27130182 107103 RMVar_ID_107103 Human_SNP_ID_415090262 m1A Human chr9 - 125241319 125241319 125241319 GTGAGGTCGACGCCGGCCAAGACAGCACAGACAGATTGACCTATTGGGGTGTTTCGCGAGTGTGA GTGAGGTCGACGCCGGCCAAGACAGCACAGACGGATTGACCTATTGGGGTGTTTCGCGAGTGTGA T C HSPA5 Ensembl:ENSG00000044574 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:125241276..125241350 26863196 MeRIP-seq:(Medium) rs1051564990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5009347,Human_RBP_ID_24285635 107104 RMVar_ID_107104 Human_SNP_ID_415112378 m1A Human chr9 - 125324690 125324690 125324690 CCACCTCTTTGACTTGCTTATGCTTGTCCTTCACCTAGAATGACCTATCTCCAACTTCTGCCAAG CCACCTCTTTGACTTGCTTATGCTTGTCCTTCGCCTAGAATGACCTATCTCCAACTTCTGCCAAG T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125324652..125324843 26863196 MeRIP-seq:(Medium) rs1203180156 Functional Loss SNV dbSNP153 33..33 33 - - - 107105 RMVar_ID_107105 Human_SNP_ID_415133903 m1A Human chr9 + 125409875 125409875 125409875 CACACACCACTCACACACCACACACACACACCACACACACAGACATATACACCAGACACACACCA CACACACCACTCACACACCACACACACACACCCCACACACAGACATATACACCAGACACACACCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:125409825..125409965 26863196 MeRIP-seq:(Medium) rs1172617415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3188326 107106 RMVar_ID_107106 Human_SNP_ID_415152350 m1A Human chr9 + 125484565 125484565 125484565 TGGCTATGTCAATTTGCGAATCCTCCTCAAAAACCCCGTCTGCCCTTGAACCTGGGGAGGAAAAG TGGCTATGTCAATTTGCGAATCCTCCTCAAAACCCCCGTCTGCCCTTGAACCTGGGGAGGAAAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125484516..125484622 26863196 MeRIP-seq:(Medium) rs770437981 Functional Loss SNV dbSNP153 33..33 33 - - - 107107 RMVar_ID_107107 Human_SNP_ID_415152351 m1A Human chr9 + 125484565 125484565 125484565 TGGCTATGTCAATTTGCGAATCCTCCTCAAAAACCCCGTCTGCCCTTGAACCTGGGGAGGAAAAG TGGCTATGTCAATTTGCGAATCCTCCTCAAAAGCCCCGTCTGCCCTTGAACCTGGGGAGGAAAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125484516..125484622 26863196 MeRIP-seq:(Medium) rs770437981 Functional Loss SNV dbSNP153 33..33 33 - - - 107108 RMVar_ID_107108 Human_SNP_ID_415154539 m1A Human chr9 + 125494087 125494087 125494087 GGGATAAAACCTAACTCTCCACTCCCTCGGTAAGACTTAAAGCTGGATGCATAAGTGAGTCACAG GGGATAAAACCTAACTCTCCACTCCCTCGGTACGACTTAAAGCTGGATGCATAAGTGAGTCACAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125494081..125494150 26863196 MeRIP-seq:(Medium) rs1376213170 Functional Loss SNV dbSNP153 33..33 33 - - - 107109 RMVar_ID_107109 Human_SNP_ID_415157315 m1A Human chr9 - 125506268 125506268 125506268 CCGCCTCGCTCCATGCCCGCTTTGTCCGTTGCAAACTTGCTTAGAAGTCATGTGTTTGGAAACGC CCGCCTCGCTCCATGCCCGCTTTGTCCGTTGCTAACTTGCTTAGAAGTCATGTGTTTGGAAACGC T A MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125506267..125506364 26863196 MeRIP-seq:(Medium) rs1366956688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6923,RMVar_hsa_circ_98768,RMVar_hsa_circ_259622,RMVar_hsa_circ_295521,RMVar_hsa_circ_259621,RMVar_hsa_circ_58147,RMVar_hsa_circ_326603,RMVar_hsa_circ_318116,RMVar_hsa_circ_13987,RMVar_hsa_circ_259623,RMVar_hsa_circ_280306,RMVar_hsa_circ_74177,RMVar_hsa_circ_53189,RMVar_hsa_circ_82712,RMVar_hsa_circ_259627,RMVar_hsa_circ_259628 107110 RMVar_ID_107110 Human_SNP_ID_415187561 m1A Human chr9 + 125631722 125631722 125631722 CGTCTCTCACCTCCTCTGCTCTCAGCCTCCACATTCCAGTCATACCCTACTACTTTCATTGCCCA CGTCTCTCACCTCCTCTGCTCTCAGCCTCCACGTTCCAGTCATACCCTACTACTTTCATTGCCCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125631717..125631788 26863196 MeRIP-seq:(Medium) rs1379244647 Functional Loss SNV dbSNP153 33..33 33 - - - 107111 RMVar_ID_107111 Human_SNP_ID_415194927 m1A Human chr9 + 125663189 125663189 125663189 TCCTTACCAGACCCTCCATAACTAGGAACCCCACTACTGACTTCTCTGATCCCACTCTTCCCGTG TCCTTACCAGACCCTCCATAACTAGGAACCCCGCTACTGACTTCTCTGATCCCACTCTTCCCGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125663186..125663489 26863196 MeRIP-seq:(Medium) rs1191445284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259644 107112 RMVar_ID_107112 Human_SNP_ID_415197165 m1A Human chr9 + 125672630 125672630 125672630 AAAAGGCTATTTTCTCCTCTTCATATTGTTTCACGAGCTCACCTACCTAGAAACATGATGTACAC AAAAGGCTATTTTCTCCTCTTCATATTGTTTCGCGAGCTCACCTACCTAGAAACATGATGTACAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:125672551..125672700 26863196 MeRIP-seq:(Medium) rs562352813 Functional Loss SNV dbSNP153 33..33 33 - - - 107113 RMVar_ID_107113 Human_SNP_ID_415197168 m1A Human chr9 - 125672636 125672636 125672636 TTTGCTGTGTACATCATGTTTCTAGGTAGGTGAGCTCGTGAAACAATATGAAGAGGAGAAAATAG TTTGCTGTGTACATCATGTTTCTAGGTAGGTGGGCTCGTGAAACAATATGAAGAGGAGAAAATAG T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr9:125672450..125672680;chr9:125672495..125696269 26863196,32194978 MeRIP-seq:(Medium) rs1217071211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8944644,Human_RBP_ID_16576030,Human_RBP_ID_26565965 Human_Splice_Rec_1080662,Human_Splice_Rec_1080702,Human_Splice_Rec_1080722,Human_Splice_Rec_1080846,Human_Splice_Rec_1080882,Human_Splice_Rec_1080890 RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_311986,RMVar_hsa_circ_326246,RMVar_hsa_circ_259639,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_259638,RMVar_hsa_circ_259641,RMVar_hsa_circ_259640,RMVar_hsa_circ_275030,RMVar_hsa_circ_259643,RMVar_hsa_circ_259645,RMVar_hsa_circ_277253,RMVar_hsa_circ_259646,RMVar_hsa_circ_369585 107114 RMVar_ID_107114 Human_SNP_ID_415206617 m1A Human chr9 + 125707178 125707178 125707178 CCCTGCTGCTCGCCGCCGCCGGCCGGCCGAGCAGCAGCCCTATTACCCCGAGCCGCACACGACCC CCCTGCTGCTCGCCGCCGCCGGCCGGCCGAGCCGCAGCCCTATTACCCCGAGCCGCACACGACCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr9:125706937..125707225;chr9:125706951..125707225 26863196 MeRIP-seq:(Medium) rs1410576155 Functional Loss SNV dbSNP153 33..33 33 - - - 107115 RMVar_ID_107115 Human_SNP_ID_415217132 m1A Human chr9 - 125746814 125746814 125746814 AGGAGGGCCCCGGCGGGCCGCGCGCCGGGCGGACAGCCGATGGATAGGGCGGGAGAAGTCGCCGC AGGAGGGCCCCGGCGGGCCGCGCGCCGGGCGGGCAGCCGATGGATAGGGCGGGAGAAGTCGCCGC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:125746726..125747025 26863410 MeRIP-seq:(Medium) rs1208890944 Functional Loss SNV dbSNP153 33..33 33 - - - 107116 RMVar_ID_107116 Human_SNP_ID_415217166 m1A Human chr9 + 125746887 125746887 125746887 AGCGCCCCCGCCGCCTCTGCCCGCCCGCTCCCAAACTTTCCTCCTCCGCCCCCCCTCGCTCCCCG AGCGCCCCCGCCGCCTCTGCCCGCCCGCTCCCTAACTTTCCTCCTCCGCCCCCCCTCGCTCCCCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:125746793..125746935 26863196 MeRIP-seq:(Medium) rs1211491007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5430928,Human_RBP_ID_5454141,Human_RBP_ID_5481700,Human_RBP_ID_5515630 107117 RMVar_ID_107117 Human_SNP_ID_415217265 m1A Human chr9 + 125747096 125747096 125747096 CGGGCGTCCCGGCAACTCGGCGGGCGCTGAGGAGCAAGTTGCGCGGGGCCGCCCGGCGGGGCGCG CGGGCGTCCCGGCAACTCGGCGGGCGCTGAGGGGCAAGTTGCGCGGGGCCGCCCGGCGGGGCGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125746783..125747131 26863196 MeRIP-seq:(Medium) rs1228052543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711920,Human_RBP_ID_5481701 107118 RMVar_ID_107118 Human_SNP_ID_415217268 m1A Human chr9 + 125747099 125747099 125747099 GCGTCCCGGCAACTCGGCGGGCGCTGAGGAGCAAGTTGCGCGGGGCCGCCCGGCGGGGCGCGCGG GCGTCCCGGCAACTCGGCGGGCGCTGAGGAGCGAGTTGCGCGGGGCCGCCCGGCGGGGCGCGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125746813..125747141 26863196 MeRIP-seq:(Medium) rs1430177591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711920,Human_RBP_ID_5481701 107119 RMVar_ID_107119 Human_SNP_ID_415217362 m1A Human chr9 - 125747297 125747297 125747297 CGCCCGCGCGGGGAGGGGGCGGCCCGGCCGGCAGGGCCCGCGGCTGAGGCGATGAGGACGGGCGC CGCCCGCGCGGGGAGGGGGCGGCCCGGCCGGCGGGGCCCGCGGCTGAGGCGATGAGGACGGGCGC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:125747251..125747369 32194978 MeRIP-seq:(Medium) rs1313295894 Functional Loss SNV dbSNP153 33..33 33 - - - 107120 RMVar_ID_107120 Human_SNP_ID_415232265 m1A Human chr9 - 125805248 125805248 125805248 CCCAAAGGCATCCACTCTGTTCCTCAAGTCCAACAAATCCTTACCACAGCCAGGCCTGTGCACTT CCCAAAGGCATCCACTCTGTTCCTCAAGTCCAGCAAATCCTTACCACAGCCAGGCCTGTGCACTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125805197..125805389 26863196 MeRIP-seq:(Medium) rs969022421 Functional Loss SNV dbSNP153 33..33 33 - - - 107121 RMVar_ID_107121 Human_SNP_ID_415257456 m1A Human chr9 - 125915650 125915647 125915650 CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGAAGCGAGAAACAGAGGACAAATAGTGTGAGTAT CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAG___CGAGAAACAGAGGACAAATAGTGTGAGTAT GCTT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125915644..125915729 26863196 MeRIP-seq:(Medium) rs750043423 Functional Loss DEL dbSNP153 33..35 33 - - - 107122 RMVar_ID_107122 Human_SNP_ID_415257457 m1A Human chr9 - 125915650 125915650 125915650 CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGAAGCGAGAAACAGAGGACAAATAGTGTGAGTAT CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGGAGCGAGAAACAGAGGACAAATAGTGTGAGTAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125915644..125915729 26863196 MeRIP-seq:(Medium) rs138144415 Functional Loss SNV dbSNP153 33..33 33 - - - 107123 RMVar_ID_107123 Human_SNP_ID_415257458 m1A Human chr9 - 125915650 125915650 125915650 CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGAAGCGAGAAACAGAGGACAAATAGTGTGAGTAT CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGCAGCGAGAAACAGAGGACAAATAGTGTGAGTAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125915644..125915729 26863196 MeRIP-seq:(Medium) rs138144415 Functional Loss SNV dbSNP153 33..33 33 - - - 107124 RMVar_ID_107124 Human_SNP_ID_415359128 m1A Human chr9 + 126326983 126326965 126326983 AGACGGAGCCGGGACCCGCCGCCGCCGCAGCCACCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA AGACGGAGCCGGGAC__________________CCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA CCCGCCGCCGCCGCAGCCA C MVB12B Ensembl:ENSG00000196814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126326747..126326995 26863196 MeRIP-seq:(Medium) rs776470041 Functional Loss DEL dbSNP153 16..33 33 - - - Human_RBP_ID_5035868 Human_Splice_Rec_1081063,Human_Splice_Rec_1081081 107125 RMVar_ID_107125 Human_SNP_ID_415359135 m1A Human chr9 + 126326983 126326968 126326983 AGACGGAGCCGGGACCCGCCGCCGCCGCAGCCACCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA AGACGGAGCCGGGACCCG_______________CCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA GCCGCCGCCGCAGCCA G MVB12B Ensembl:ENSG00000196814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126326747..126326995 26863196 MeRIP-seq:(Medium) rs759101608 Functional Loss DEL dbSNP153 19..33 33 - - - Human_RBP_ID_5035868 Human_Splice_Rec_1081063,Human_Splice_Rec_1081081 107126 RMVar_ID_107126 Human_SNP_ID_415359138 m1A Human chr9 + 126326983 126326974 126326983 AGACGGAGCCGGGACCCGCCGCCGCCGCAGCCACCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA AGACGGAGCCGGGACCCGCCGCCG_________CCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA GCCGCAGCCA G MVB12B Ensembl:ENSG00000196814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126326747..126326995 26863196 MeRIP-seq:(Medium) rs1169716303 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_5035868 Human_Splice_Rec_1081063,Human_Splice_Rec_1081081 107127 RMVar_ID_107127 Human_SNP_ID_415359149 m1A Human chr9 + 126326983 126326983 126326983 AGACGGAGCCGGGACCCGCCGCCGCCGCAGCCACCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA AGACGGAGCCGGGACCCGCCGCCGCCGCAGCCGCCGCCGCCGCCGCCCCAGCGGGGAACAGTTAA A G MVB12B Ensembl:ENSG00000196814 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126326747..126326995 26863196 MeRIP-seq:(Medium) rs1251175213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035868 Human_Splice_Rec_1081063,Human_Splice_Rec_1081081 107128 RMVar_ID_107128 Human_SNP_ID_415400948 m1A Human chr9 - 126504839 126504817 126504839 TCCCATGACAAGGTCCTGCTGCTGTGCCACCCAGGAGTCCTGAGAAGGCCACCCCCACCAGGGGC TCCCATGACAAGGTCCTGCTGCTGTGCCACCC______________________CCACCAGGGGC GGGGTGGCCTTCTCAGGACTCCT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:126504791..126504918 32194978 MeRIP-seq:(Medium) rs1198510833 Functional Loss DEL dbSNP153 33..54 33 - - - 107129 RMVar_ID_107129 Human_SNP_ID_415428884 m1A Human chr9 + 126614029 126614029 126614029 GGAGCCCCGCGGCCCGCTGCGCCCCGCCCGGGACCCCGCTGCGCCGCGCGCCCCCCCCGCGGCCC GGAGCCCCGCGGCCCGCTGCGCCCCGCCCGGGCCCCCGCTGCGCCGCGCGCCCCCCCCGCGGCCC A C LMX1B Ensembl:ENSG00000136944 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:126613951..126614186 26863410 MeRIP-seq:(Medium) rs1195474167 Functional Loss SNV dbSNP153 33..33 33 - - - 107130 RMVar_ID_107130 Human_SNP_ID_415428885 m1A Human chr9 + 126614029 126614029 126614029 GGAGCCCCGCGGCCCGCTGCGCCCCGCCCGGGACCCCGCTGCGCCGCGCGCCCCCCCCGCGGCCC GGAGCCCCGCGGCCCGCTGCGCCCCGCCCGGGGCCCCGCTGCGCCGCGCGCCCCCCCCGCGGCCC A G LMX1B Ensembl:ENSG00000136944 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:126613951..126614186 26863410 MeRIP-seq:(Medium) rs1195474167 Functional Loss SNV dbSNP153 33..33 33 - - - 107131 RMVar_ID_107131 Human_SNP_ID_415428934 m1A Human chr9 - 126614090 126614090 126614090 GCGGTGGCGGTGGCGGCGGCGGCAGGCGGGGGAGGGGGTGGGGGTGCAGGGGCGGCCCCGCGGGC GCGGTGGCGGTGGCGGCGGCGGCAGGCGGGGGGGGGGGTGGGGGTGCAGGGGCGGCCCCGCGGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:126613945..126614227 26863196 MeRIP-seq:(Medium) rs905356439 Functional Loss SNV dbSNP153 33..33 33 - - - 107132 RMVar_ID_107132 Human_SNP_ID_415493929 m1A Human chr9 - 126862103 126862103 126862103 CCCTCACTAAACCCTCCCTAACCACTCGGCCTACAGTGACCTCCATCTCTCCTTCTTAATTCTAC CCCTCACTAAACCCTCCCTAACCACTCGGCCTGCAGTGACCTCCATCTCTCCTTCTTAATTCTAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:126862096..126862231 26863196 MeRIP-seq:(Medium) rs902369555 Functional Loss SNV dbSNP153 33..33 33 - - - 107133 RMVar_ID_107133 Human_SNP_ID_415498595 m1A Human chr9 + 126880054 126880054 126880054 GCAGTGGGAGCGTTTCTGAATATGAGATTCAGATAGAGGGAGACCATGAGCAAGGAGACCTATTG GCAGTGGGAGCGTTTCTGAATATGAGATTCAGCTAGAGGGAGACCATGAGCAAGGAGACCTATTG A C ZBTB34 Ensembl:ENSG00000177125 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:126880009..126880169 26863196 MeRIP-seq:(Medium) rs778144722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18903816 RMVar_hsa_circ_86848,RMVar_hsa_circ_259677,RMVar_hsa_circ_259676 107134 RMVar_ID_107134 Human_SNP_ID_415498596 m1A Human chr9 + 126880054 126880054 126880054 GCAGTGGGAGCGTTTCTGAATATGAGATTCAGATAGAGGGAGACCATGAGCAAGGAGACCTATTG GCAGTGGGAGCGTTTCTGAATATGAGATTCAGGTAGAGGGAGACCATGAGCAAGGAGACCTATTG A G ZBTB34 Ensembl:ENSG00000177125 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:126880009..126880169 26863196 MeRIP-seq:(Medium) rs778144722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18903816 RMVar_hsa_circ_86848,RMVar_hsa_circ_259677,RMVar_hsa_circ_259676 107135 RMVar_ID_107135 Human_SNP_ID_415507605 m1A Human chr9 - 126914896 126914896 126914896 AGCGGCCCAGCGGCAGCGGCGCCTTCGCTTGGAGGCCGGGGCCACGCCGAGCCGGGCCGGGGCCG AGCGGCCCAGCGGCAGCGGCGCCTTCGCTTGGCGGCCGGGGCCACGCCGAGCCGGGCCGGGGCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126914846..126914914 26863196 MeRIP-seq:(Medium) rs1399460519 Functional Loss SNV dbSNP153 33..33 33 - - - 107136 RMVar_ID_107136 Human_SNP_ID_415555593 m1A Human chr9 + 127118476 127118474 127118476 ATTCAATGAATTGATTCTTTCTTGAGATTTCCACAGTGTGGTTGTCCAGGATGGCAGCAGGCTGG ATTCAATGAATTGATTCTTTCTTGAGATTTC__CAGTGTGGTTGTCCAGGATGGCAGCAGGCTGG CCA C RALGPS1 Ensembl:ENSG00000136828 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127118469..127118623 32194978 MeRIP-seq:(Medium) rs373323757 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9232985 RMVar_hsa_circ_35484,RMVar_hsa_circ_126969,RMVar_hsa_circ_20930,RMVar_hsa_circ_108703,RMVar_hsa_circ_259684,RMVar_hsa_circ_368395,RMVar_hsa_circ_279919,RMVar_hsa_circ_110333,RMVar_hsa_circ_259690,RMVar_hsa_circ_259691,RMVar_hsa_circ_349416 107137 RMVar_ID_107137 Human_SNP_ID_415571711 m1A Human chr9 + 127186909 127186898 127186910 GAGGGAGAGTCAAGAATTGAATGGAAGAGACCAAGGGCAAGTCCAGTGGGTTTGGGAGAGACTGG GAGGGAGAGTCAAGAATTGAAT____________GGGCAAGTCCAGTGGGTTTGGGAGAGACTGG TGGAAGAGACCAA T RALGPS1 Ensembl:ENSG00000136828 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127186871..127187039 26863196 MeRIP-seq:(Medium) rs1194370855 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_126969,RMVar_hsa_circ_108703,RMVar_hsa_circ_259684,RMVar_hsa_circ_259691,RMVar_hsa_circ_267293 107138 RMVar_ID_107138 Human_SNP_ID_415581315 m1A Human chr9 + 127225278 127225278 127225278 CCGAGCGGCCGGCCGAGGCCCGAGCCCACCCGAGTGCGCCCGAGCCCGCGGCCCCCGCCCGGGGC CCGAGCGGCCGGCCGAGGCCCGAGCCCACCCGGGTGCGCCCGAGCCCGCGGCCCCCGCCCGGGGC A G GARNL3 Ensembl:ENSG00000136895 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127225239..127225358 26863196 MeRIP-seq:(Medium) rs1373298729 Functional Loss SNV dbSNP153 33..33 33 - - - 107139 RMVar_ID_107139 Human_SNP_ID_415623156 m1A Human chr9 + 127407453 127407453 127407453 TGCCTCCTGTTCCAGCTCCTGCTGCTGCTCTGAGGACTCAGGAACACCTTCGAGCTTTGCAGACC TGCCTCCTGTTCCAGCTCCTGCTGCTGCTCTGGGGACTCAGGAACACCTTCGAGCTTTGCAGACC A G SLC2A8 Ensembl:ENSG00000136856 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127404756..127407626 32194978 MeRIP-seq:(Medium) rs1260024770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712115,Human_RBP_ID_5124012 Human_Splice_Rec_1081908,Human_Splice_Rec_1081922,Human_Splice_Rec_1081923,Human_Splice_Rec_1081927 RMVar_hsa_circ_259728 107140 RMVar_ID_107140 Human_SNP_ID_415628040 m1A Human chr9 + 127424795 127424795 127424795 GGCTGTGGCGCGAGGCGGGACTCAAATGCTGGAGGAAGGAGGTGAGGAGTGGTAGAGGGAGCGAT GGCTGTGGCGCGAGGCGGGACTCAAATGCTGGGGGAAGGAGGTGAGGAGTGGTAGAGGGAGCGAT A G ZNF79 Ensembl:ENSG00000196152 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127424746..127424868 26863196 MeRIP-seq:(Medium) rs78632032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92694 Human_Splice_Rec_1081941,Human_Splice_Rec_1081951 107141 RMVar_ID_107141 Human_SNP_ID_415634283 m1A Human chr9 + 127447738 127447738 127447738 TGTTTTCCTTTGTGCTTAACTCTGTGGGAAAGAAAAAAAAAATCAGTAAAAAGTTTAAAAGGATT TGTTTTCCTTTGTGCTTAACTCTGTGGGAAAGGAAAAAAAAATCAGTAAAAAGTTTAAAAGGATT A G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127447722..127447821 32194978 MeRIP-seq:(Medium) rs767040404 Functional Loss SNV dbSNP153 33..33 33 - - - 107142 RMVar_ID_107142 Human_SNP_ID_415635600 m1A Human chr9 + 127451349 127451349 127451349 TGGTGGAGGCGGCTGGTGTCGGATGAACCCGGATTCGGGACGACCGAAGGAAGTTGCACCTTGGC TGGTGGAGGCGGCTGGTGTCGGATGAACCCGGGTTCGGGACGACCGAAGGAAGTTGCACCTTGGC A G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127451301..127451400 26863196 MeRIP-seq:(Medium) rs748172463 Functional Loss SNV dbSNP153 33..33 33 - - - 107143 RMVar_ID_107143 Human_SNP_ID_415635606 m1A Human chr9 + 127451356 127451356 127451356 GGCGGCTGGTGTCGGATGAACCCGGATTCGGGACGACCGAAGGAAGTTGCACCTTGGCCTCCTCC GGCGGCTGGTGTCGGATGAACCCGGATTCGGGGCGACCGAAGGAAGTTGCACCTTGGCCTCCTCC A G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr9:127451189..127451400;chr9:127451326..127451400 26863196 MeRIP-seq:(Medium) rs1184037057 Functional Loss SNV dbSNP153 33..33 33 - - - 107144 RMVar_ID_107144 Human_SNP_ID_415635612 m1A Human chr9 + 127451363 127451363 127451363 GGTGTCGGATGAACCCGGATTCGGGACGACCGAAGGAAGTTGCACCTTGGCCTCCTCCGAGCCGA GGTGTCGGATGAACCCGGATTCGGGACGACCGCAGGAAGTTGCACCTTGGCCTCCTCCGAGCCGA A C RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:127451276..127451405;chr9:127450767..127451400 32194978 MeRIP-seq:(Medium) rs756820785 Functional Loss SNV dbSNP153 33..33 33 - - - 107145 RMVar_ID_107145 Human_SNP_ID_415635726 m1A Human chr9 - 127451628 127451628 127451628 ATATGGGAAACAGCTAGGGCTGGGATCACCGGAGCCACCCTTCTCAGACTTCTCCGGAGCGAACT ATATGGGAAACAGCTAGGGCTGGGATCACCGGGGCCACCCTTCTCAGACTTCTCCGGAGCGAACT T C RF00017-4541,RF00017-4552 RNACentral:URS0000992647,RNACentral:URS0000973F83 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127451577..127451669 26863196 MeRIP-seq:(Medium) rs878946759 Functional Loss SNV dbSNP153 33..33 33 - - - 107146 RMVar_ID_107146 Human_SNP_ID_415640363 m1A Human chr9 + 127468332 127468331 127468333 CAGGGAGGAGAAGGGATTGGAGGAGGAAAGAAAGAGTGCAGGACAGGGGACCAGTTAGGAGGCTG CAGGGAGGAGAAGGGATTGGAGGAGGAAAGAA__AGTGCAGGACAGGGGACCAGTTAGGAGGCTG AAG A LRSAM1 Ensembl:ENSG00000148356 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127468126..127468390 26863196 MeRIP-seq:(Medium) rs1022535788 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_9925,RMVar_hsa_circ_121391,RMVar_hsa_circ_30622,RMVar_hsa_circ_45034,RMVar_hsa_circ_13371,RMVar_hsa_circ_259753,RMVar_hsa_circ_276244,RMVar_hsa_circ_259754 107147 RMVar_ID_107147 Human_SNP_ID_415640366 m1A Human chr9 + 127468342 127468342 127468342 AAGGGATTGGAGGAGGAAAGAAAGAGTGCAGGACAGGGGACCAGTTAGGAGGCTGTCGGGGTCAT AAGGGATTGGAGGAGGAAAGAAAGAGTGCAGGTCAGGGGACCAGTTAGGAGGCTGTCGGGGTCAT A T LRSAM1 Ensembl:ENSG00000148356 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:127468229..127468358 26863196 MeRIP-seq:(Medium) rs531158843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9925,RMVar_hsa_circ_121391,RMVar_hsa_circ_30622,RMVar_hsa_circ_45034,RMVar_hsa_circ_13371,RMVar_hsa_circ_259753,RMVar_hsa_circ_276244,RMVar_hsa_circ_259754 107148 RMVar_ID_107148 Human_SNP_ID_415650319 m1A Human chr9 + 127505843 127505843 127505843 TTCAGAGGGAGGTGACTTGGTGACTGAGAGGCAGCAGAGGCCAAAGCCTGACCCCAGACCCTCAG TTCAGAGGGAGGTGACTTGGTGACTGAGAGGCGGCAGAGGCCAAAGCCTGACCCCAGACCCTCAG A G RF00017-1003,RF00017-4495 RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:127505776..127506000 26863196 MeRIP-seq:(Medium) rs887060819 Functional Loss SNV dbSNP153 33..33 33 - - - 107149 RMVar_ID_107149 Human_SNP_ID_415650401 m1A Human chr9 + 127506157 127506157 127506157 TCACTCAGCCATCTCACTCACTCACTCCCAGCATCCCCCAGGATGGGGGTCCCCTCCTTCACTCA TCACTCAGCCATCTCACTCACTCACTCCCAGCGTCCCCCAGGATGGGGGTCCCCTCCTTCACTCA A G RF00017-1003,RF00017-4495 RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127506033..127506376 26863196 MeRIP-seq:(Medium) rs1425752271 Functional Loss SNV dbSNP153 33..33 33 - - - 107150 RMVar_ID_107150 Human_SNP_ID_415650520 m1A Human chr9 + 127506652 127506650 127506652 CCCCTGCATCTGAGATCATCCCACAGAAGAGAAAACAGGGAGCAAGAAAGTGTTGACTGAACCCA CCCCTGCATCTGAGATCATCCCACAGAAGAG__AACAGGGAGCAAGAAAGTGTTGACTGAACCCA GAA G RF00017-1003,RF00017-4495 RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127506601..127507175 26863196 MeRIP-seq:(Medium) rs1223360071 Functional Loss DEL dbSNP153 32..33 33 - - - 107151 RMVar_ID_107151 Human_SNP_ID_415650724 m1A Human chr9 - 127507124 127507124 127507124 CCTGCGTCCCCGGACGGTGTCACTGAGATCCGAGGCCTGCTGGCCCAAGGTCTGCGGCCTGAGAG CCTGCGTCCCCGGACGGTGTCACTGAGATCCGCGGCCTGCTGGCCCAAGGTCTGCGGCCTGAGAG T G NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127506601..127507441;chr9:127506552..127507450;chr9:127506526..127507425 26863196 MeRIP-seq:(Medium) rs764778214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22118866 Human_miRNA_ID_2221476,Human_miRNA_ID_2484530,Human_miRNA_ID_2662095,Human_miRNA_ID_2680544,Human_miRNA_ID_3072906 RMVar_hsa_circ_82895,RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259758,RMVar_hsa_circ_259760,RMVar_hsa_circ_79707,RMVar_hsa_circ_259759,RMVar_hsa_circ_118710,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_101103,RMVar_hsa_circ_90450,RMVar_hsa_circ_259765,RMVar_hsa_circ_259762,RMVar_hsa_circ_259763,RMVar_hsa_circ_259761 107152 RMVar_ID_107152 Human_SNP_ID_415650887 m1A Human chr9 - 127507433 127507433 127507433 GCTGTGTCCTGACCCTTCCCCTGTGGCCCTGTAGCTGTGAAGGAGGCCGCGGTGCAGAGGAAGCA GCTGTGTCCTGACCCTTCCCCTGTGGCCCTGTGGCTGTGAAGGAGGCCGCGGTGCAGAGGAAGCA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127507426..127507450 26863196 MeRIP-seq:(Medium) rs111318680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82895,RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259758,RMVar_hsa_circ_259760,RMVar_hsa_circ_79707,RMVar_hsa_circ_259759,RMVar_hsa_circ_118710,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_101103,RMVar_hsa_circ_90450,RMVar_hsa_circ_259765,RMVar_hsa_circ_259762,RMVar_hsa_circ_259763,RMVar_hsa_circ_259761 107153 RMVar_ID_107153 Human_SNP_ID_415651649 m1A Human chr9 - 127509700 127509700 127509700 TAAGGAAGAATTCACAAGTCACGCGCCCTCCAAATGGAGACAGCCGTTGCCCTTACTTGACCTCA TAAGGAAGAATTCACAAGTCACGCGCCCTCCAGATGGAGACAGCCGTTGCCCTTACTTGACCTCA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127509657..127509762 26863196 MeRIP-seq:(Medium) rs762550993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974801 RMVar_hsa_circ_82895,RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259759,RMVar_hsa_circ_118710,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_101103,RMVar_hsa_circ_259765,RMVar_hsa_circ_259762,RMVar_hsa_circ_259763,RMVar_hsa_circ_89281,RMVar_hsa_circ_122936,RMVar_hsa_circ_98775,RMVar_hsa_circ_259768,RMVar_hsa_circ_259769,RMVar_hsa_circ_259767 107154 RMVar_ID_107154 Human_SNP_ID_415651786 m1A Human chr9 + 127509880 127509880 127509880 CTCTCCTTCCCTCCTTCCCTCTCTTCTGTTAAATTCTTTTCTATTTTAGCACCACTCTTGGTTTC CTCTCCTTCCCTCCTTCCCTCTCTTCTGTTAATTTCTTTTCTATTTTAGCACCACTCTTGGTTTC A T RF00017-1003,RF00017-4495 RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127509878..127510016 26863196 MeRIP-seq:(Medium) rs1437317014 Functional Loss SNV dbSNP153 33..33 33 - - - 107155 RMVar_ID_107155 Human_SNP_ID_415651893 m1A Human chr9 - 127510199 127510199 127510199 CTGAGGTGCGAGATGTCTTCTTCAAGGAGGTCACGGACATGAACCTGAACGTCATCAACGAGGGC CTGAGGTGCGAGATGTCTTCTTCAAGGAGGTCGCGGACATGAACCTGAACGTCATCAACGAGGGC T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127510126..127510238 32194978 MeRIP-seq:(Medium) rs768713976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91148,Human_RBP_ID_1057993,Human_RBP_ID_8696970,Human_RBP_ID_8925463,Human_RBP_ID_18453080 Human_Splice_Rec_1082281,Human_Splice_Rec_1082311 RMVar_hsa_circ_82895,RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259759,RMVar_hsa_circ_118710,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_101103,RMVar_hsa_circ_259765,RMVar_hsa_circ_259762,RMVar_hsa_circ_259763,RMVar_hsa_circ_7962,RMVar_hsa_circ_89281,RMVar_hsa_circ_122936,RMVar_hsa_circ_98775,RMVar_hsa_circ_259768,RMVar_hsa_circ_259769,RMVar_hsa_circ_259767,RMVar_hsa_circ_346970,RMVar_hsa_circ_91870,RMVar_hsa_circ_259771,RMVar_hsa_circ_259772 107156 RMVar_ID_107156 Human_SNP_ID_415655636 m1A Human chr9 - 127523826 127523826 127523826 CTGTCTCCACAGGGACCACGGCAAAGTCGGGCAGTGCCCCCATCCTCAAGTGCCCCACACAGTTC CTGTCTCCACAGGGACCACGGCAAAGTCGGGCGGTGCCCCCATCCTCAAGTGCCCCACACAGTTC T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:127523776..127523850 26863196 MeRIP-seq:(Medium) rs944462596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1226145 Human_Splice_Rec_1082272,Human_Splice_Rec_1082302 Human_miRNA_ID_1025230,Human_miRNA_ID_2466495 RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_259765,RMVar_hsa_circ_122231,RMVar_hsa_circ_7962,RMVar_hsa_circ_122936,RMVar_hsa_circ_98775,RMVar_hsa_circ_259768,RMVar_hsa_circ_259769,RMVar_hsa_circ_346970,RMVar_hsa_circ_91870,RMVar_hsa_circ_48174,RMVar_hsa_circ_259771,RMVar_hsa_circ_259772,RMVar_hsa_circ_357415,RMVar_hsa_circ_43685,RMVar_hsa_circ_343610,RMVar_hsa_circ_259773,RMVar_hsa_circ_259774,RMVar_hsa_circ_259775,RMVar_hsa_circ_275532,RMVar_hsa_circ_317016,RMVar_hsa_circ_259776 107157 RMVar_ID_107157 Human_SNP_ID_415656598 m1A Human chr9 + 127527216 127527216 127527216 CAGGCCTCACCGCTTTGTTTTCGTAGAGCACCAGCCCGTAGTTGTGGGGCACGAGGCTGAAGCGG CAGGCCTCACCGCTTTGTTTTCGTAGAGCACCGGCCCGTAGTTGTGGGGCACGAGGCTGAAGCGG A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127525053..127561176 32194978 MeRIP-seq:(Medium) rs1422100447 Functional Loss SNV dbSNP153 33..33 33 - - - 107158 RMVar_ID_107158 Human_SNP_ID_415657804 m1A Human chr9 - 127531775 127531775 127531775 TCAAGCTCCTGCTTGTCCTTCTCTTCCAGAAAAAACCGGGAAGATCCTGACGGAGTTCCTCCAGT TCAAGCTCCTGCTTGTCCTTCTCTTCCAGAAACAACCGGGAAGATCCTGACGGAGTTCCTCCAGT T G NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127531726..127531800 26863196 MeRIP-seq:(Medium) rs139344456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1082266,Human_Splice_Rec_1082294,Human_Splice_Rec_1082296,Human_Splice_Rec_1082322 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_122936,RMVar_hsa_circ_259769,RMVar_hsa_circ_346970,RMVar_hsa_circ_259772,RMVar_hsa_circ_357415,RMVar_hsa_circ_43685,RMVar_hsa_circ_343610,RMVar_hsa_circ_90935,RMVar_hsa_circ_259774,RMVar_hsa_circ_275532,RMVar_hsa_circ_259776,RMVar_hsa_circ_259778 107159 RMVar_ID_107159 Human_SNP_ID_415667024 m1A Human chr9 - 127568983 127568980 127568983 AGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGGGCGGGCCGGGCTCCATGG AGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGG___GGGGGAAGCAGGGCGGGCCGGGCTCCATGG CGCT C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:127568889..127569026 26863196 MeRIP-seq:(Medium) rs1564322812 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_91154,Human_RBP_ID_3975769,Human_RBP_ID_5037106,Human_RBP_ID_5090924,Human_RBP_ID_5243873,Human_RBP_ID_5329610,Human_RBP_ID_5409993,Human_RBP_ID_8731115,Human_RBP_ID_9339059,Human_RBP_ID_9441742,Human_RBP_ID_18427789,Human_RBP_ID_18467864 Human_miRNA_ID_2380711,Human_miRNA_ID_3023725 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 107160 RMVar_ID_107160 Human_SNP_ID_415667025 m1A Human chr9 - 127568983 127568983 127568983 AGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGGGCGGGCCGGGCTCCATGG AGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGGGGCGGGGGAAGCAGGGCGGGCCGGGCTCCATGG T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:127568889..127569026 26863196 MeRIP-seq:(Medium) rs905036721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91154,Human_RBP_ID_3975769,Human_RBP_ID_5037106,Human_RBP_ID_5090924,Human_RBP_ID_5243873,Human_RBP_ID_5329610,Human_RBP_ID_5409993,Human_RBP_ID_8731115,Human_RBP_ID_9339059,Human_RBP_ID_9441742,Human_RBP_ID_18427789,Human_RBP_ID_18467864 Human_miRNA_ID_2380711,Human_miRNA_ID_3023725 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 107161 RMVar_ID_107161 Human_SNP_ID_415667033 m1A Human chr9 - 127569001 127569000 127569001 AGCCGGAGCGGAAGCCGCAGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGG AGCCGGAGCGGAAGCCGCAGCCGGGCGGCGGG_GCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGG CT C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:127568953..127569065 26863410 MeRIP-seq:(Medium) rs1338011790 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5035878,Human_RBP_ID_5090924,Human_RBP_ID_5409993,Human_RBP_ID_9339059,Human_RBP_ID_9442023,Human_RBP_ID_18427220 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 107162 RMVar_ID_107162 Human_SNP_ID_415667034 m1A Human chr9 - 127569001 127569001 127569001 AGCCGGAGCGGAAGCCGCAGCCGGGCGGCGGGAGCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGG AGCCGGAGCGGAAGCCGCAGCCGGGCGGCGGGGGCGGCGGGAGCGGCGGGAGCGGGGGAAGCAGG T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:127568953..127569065 26863410 MeRIP-seq:(Medium) rs867930561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035878,Human_RBP_ID_5090924,Human_RBP_ID_5409993,Human_RBP_ID_9339059,Human_RBP_ID_9442023,Human_RBP_ID_18427220 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 107163 RMVar_ID_107163 Human_SNP_ID_415678072 m1A Human chr9 - 127612351 127612351 127612351 GCTCCGATCTCCTCGTCCCGCGACGCCTGCGGACCCCGCCGCCTCCTCAGGTGGGCGCGCTGGGC GCTCCGATCTCCTCGTCCCGCGACGCCTGCGGCCCCCGCCGCCTCCTCAGGTGGGCGCGCTGGGC T G RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127612301..127613476 32194978 MeRIP-seq:(Medium) rs562125563 Functional Loss SNV dbSNP153 33..33 33 - - - 107164 RMVar_ID_107164 Human_SNP_ID_415678102 m1A Human chr9 + 127612404 127612404 127612404 GGAGATCGGAGCCGGGAGACTCGCGCAGCGCCATGGCCCCCATTGGCCTCAAAGCTGTTGTCGGA GGAGATCGGAGCCGGGAGACTCGCGCAGCGCCCTGGCCCCCATTGGCCTCAAAGCTGTTGTCGGA A C STXBP1 Ensembl:ENSG00000136854 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:127612298..127612450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1226148,Human_RBP_ID_5036419,Human_RBP_ID_8697014,Human_RBP_ID_17715901,Human_RBP_ID_26362101 Human_Splice_Rec_1082465,Human_Splice_Rec_1082503,Human_Splice_Rec_1082541,Human_Splice_Rec_1082579,Human_Splice_Rec_1082615,Human_Splice_Rec_1082653,Human_Splice_Rec_1082691,Human_Splice_Rec_1082729,Human_Splice_Rec_1082741,Human_Splice_Rec_1082751,Human_Splice_Rec_1082787,Human_Splice_Rec_1082827 Human_miRNA_ID_2975631 RMVar_hsa_circ_120746,RMVar_hsa_circ_259779 107165 RMVar_ID_107165 Human_SNP_ID_415678116 m1A Human chr9 + 127612436 127612434 127612436 ATGGCCCCCATTGGCCTCAAAGCTGTTGTCGGAGAGAGTAAGTGGAGCCGGGATCCTTCCAGCAG ATGGCCCCCATTGGCCTCAAAGCTGTTGTCG__GAGAGTAAGTGGAGCCGGGATCCTTCCAGCAG GGA G STXBP1 Ensembl:ENSG00000136854 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127612250..127612496;chr9:127612256..127612495 26863196 MeRIP-seq:(Medium) rs1057518331 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1082465,Human_Splice_Rec_1082503,Human_Splice_Rec_1082541,Human_Splice_Rec_1082579,Human_Splice_Rec_1082615,Human_Splice_Rec_1082653,Human_Splice_Rec_1082691,Human_Splice_Rec_1082729,Human_Splice_Rec_1082741,Human_Splice_Rec_1082751,Human_Splice_Rec_1082787,Human_Splice_Rec_1082827 RMVar_hsa_circ_120746,RMVar_hsa_circ_259779 107166 RMVar_ID_107166 Human_SNP_ID_415687398 m1A Human chr9 + 127651538 127651538 127651538 AGCCTAAGGTGGGAAATGACCTTATCTAACAGAGAGGTGTAGACGTCTTTGATATTACATTAATT AGCCTAAGGTGGGAAATGACCTTATCTAACAGGGAGGTGTAGACGTCTTTGATATTACATTAATT A G STXBP1 Ensembl:ENSG00000136854 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127651534..127651629 26863196 MeRIP-seq:(Medium) rs1018107287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63401,RMVar_hsa_circ_120746,RMVar_hsa_circ_259779 107167 RMVar_ID_107167 Human_SNP_ID_415696342 m1A Human chr9 - 127690867 127690867 127690867 GCTGTGGGATGGGGGCGTGTTTTGGAGGGGCGACTTATTTTTTTAACTGCTTATTTCTTCATCTG GCTGTGGGATGGGGGCGTGTTTTGGAGGGGCGTCTTATTTTTTTAACTGCTTATTTCTTCATCTG T A PTRH1 Ensembl:ENSG00000187024 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127690822..127691025 26863196 MeRIP-seq:(Medium) rs768590562 Functional Loss SNV dbSNP153 33..33 33 - - - 107168 RMVar_ID_107168 Human_SNP_ID_415696343 m1A Human chr9 - 127690867 127690867 127690867 GCTGTGGGATGGGGGCGTGTTTTGGAGGGGCGACTTATTTTTTTAACTGCTTATTTCTTCATCTG GCTGTGGGATGGGGGCGTGTTTTGGAGGGGCGGCTTATTTTTTTAACTGCTTATTTCTTCATCTG T C PTRH1 Ensembl:ENSG00000187024 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127690822..127691025 26863196 MeRIP-seq:(Medium) rs768590562 Functional Loss SNV dbSNP153 33..33 33 - - - 107169 RMVar_ID_107169 Human_SNP_ID_415702748 m1A Human chr9 - 127715067 127715067 127715067 GAGTTGGACGCGCGACCGGCACTGTGCCGCCGACCTCGCCCTGGCCCCGCTGGGGGATGCCCAAC GAGTTGGACGCGCGACCGGCACTGTGCCGCCGTCCTCGCCCTGGCCCCGCTGGGGGATGCCCAAC T A PTRH1 Ensembl:ENSG00000187024 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:127715021..127715176 26863196 MeRIP-seq:(Medium) rs1336207444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1082923,Human_Splice_Rec_1082931,Human_Splice_Rec_1082939,Human_Splice_Rec_1082947,Human_Splice_Rec_1082955,Human_Splice_Rec_1082961 107170 RMVar_ID_107170 Human_SNP_ID_415702785 m1A Human chr9 + 127715136 127715136 127715136 CCACACCCAGCCGCCGCGCCAGCTGCCCCAGCACCGCCATGCCCACGCTGTGTCGCGTGCCGGGC CCACACCCAGCCGCCGCGCCAGCTGCCCCAGCGCCGCCATGCCCACGCTGTGTCGCGTGCCGGGC A G CFAP157 Ensembl:ENSG00000160401 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127714615..127715675;chr9:127715001..127715469;chr9:127715036..127715229 26863196 MeRIP-seq:(Medium) rs753301562 Functional Loss SNV dbSNP153 33..33 33 - - - 107171 RMVar_ID_107171 Human_SNP_ID_415702788 m1A Human chr9 + 127715142 127715142 127715142 CCAGCCGCCGCGCCAGCTGCCCCAGCACCGCCATGCCCACGCTGTGTCGCGTGCCGGGCAGTCCG CCAGCCGCCGCGCCAGCTGCCCCAGCACCGCCGTGCCCACGCTGTGTCGCGTGCCGGGCAGTCCG A G CFAP157 Ensembl:ENSG00000160401 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr9:127715057..127715200;chr9:127715094..127715234 26863196 MeRIP-seq:(Medium) rs1214988748 Functional Loss SNV dbSNP153 33..33 33 - - - 107172 RMVar_ID_107172 Human_SNP_ID_415702995 m1A Human chr9 + 127715602 127715592 127715602 GCTCCAAAACACATCGGCTCATGGCTCTACTCAGCCGCTGTCCGGCGCCCAAAAAGCCGCCCGGC GCTCCAAAACACATCGGCTCATG__________GCCGCTGTCCGGCGCCCAAAAAGCCGCCCGGC GGCTCTACTCA G CFAP157 Ensembl:ENSG00000160401 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127715494..127715650 26863196 MeRIP-seq:(Medium) rs746816297 Functional Loss DEL dbSNP153 24..33 33 - - - 107173 RMVar_ID_107173 Human_SNP_ID_415708006 m1A Human chr9 - 127731764 127731764 127731764 CTGCAGCCTGAGCCTTCTTACTGTGAATTATAACTCAGGGACTGTGGCTCGTGGCGGTGCTCCCT CTGCAGCCTGAGCCTTCTTACTGTGAATTATATCTCAGGGACTGTGGCTCGTGGCGGTGCTCCCT T A TOR2A Ensembl:ENSG00000160404 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127731713..127731785 26863196 MeRIP-seq:(Medium) rs1347428277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712227,Human_RBP_ID_21907214,Human_RBP_ID_27370445 107174 RMVar_ID_107174 Human_SNP_ID_415709125 m1A Human chr9 + 127735209 127735209 127735209 AAGCCAGGTCCCAGGCGGCGGCCGCGGCCGAGACCAGCCCGAGCAGCCCGAGGAGCGAGCCCCAG AAGCCAGGTCCCAGGCGGCGGCCGCGGCCGAGGCCAGCCCGAGCAGCCCGAGGAGCGAGCCCCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:127735126..127735275 26863410 MeRIP-seq:(Medium) rs1400347040 Functional Loss SNV dbSNP153 33..33 33 - - - 107175 RMVar_ID_107175 Human_SNP_ID_415722345 m1A Human chr9 + 127785646 127785646 127785646 GCCCCGGGCCCGGGTCCGGCCAGGGAGCTCCCAGGCCGCGGCTCGGGGGCTGACCCCCCGCCCGC GCCCCGGGCCCGGGTCCGGCCAGGGAGCTCCCCGGCCGCGGCTCGGGGGCTGACCCCCCGCCCGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127785596..127785835 26863196 MeRIP-seq:(Medium) rs1385342889 Functional Loss SNV dbSNP153 33..33 33 - - - 107176 RMVar_ID_107176 Human_SNP_ID_415722588 m1A Human chr9 + 127786112 127786112 127786112 GCGGCGGGACCCGGAGCAGGAGCGGCGGCAGCAGCGACTGGGGGCGGCGGCGGCGCGTTGGAGGC GCGGCGGGACCCGGAGCAGGAGCGGCGGCAGCGGCGACTGGGGGCGGCGGCGGCGCGTTGGAGGC A G CDK9 Ensembl:ENSG00000136807 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127786035..127786261;chr9:127785530..127786809;chr9:127785976..127786739 26863196 MeRIP-seq:(Medium) rs1286065733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256635,Human_RBP_ID_798204,Human_RBP_ID_5010260,Human_RBP_ID_9339063,Human_RBP_ID_23094488,Human_RBP_ID_26361119 107177 RMVar_ID_107177 Human_SNP_ID_415722621 m1A Human chr9 - 127786150 127786150 127786150 AAGGGCACTCCACCGAGTCGTACTGCTTTGCCATGGCCGCCTCCAACGCGCCGCCGCCGCCCCCA AAGGGCACTCCACCGAGTCGTACTGCTTTGCCCTGGCCGCCTCCAACGCGCCGCCGCCGCCCCCA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:127786057..127786174 26863196 MeRIP-seq:(Medium) rs1448871251 Functional Loss SNV dbSNP153 33..33 33 - - - 107178 RMVar_ID_107178 Human_SNP_ID_415723967 m1A Human chr9 + 127789398 127789398 127789398 CTTCTGGTCCGACCCCATGCCCTCCGACCTCAAGGGCATGCTCTCCACCCACCTGACGTCCATGT CTTCTGGTCCGACCCCATGCCCTCCGACCTCAGGGGCATGCTCTCCACCCACCTGACGTCCATGT A G CDK9 Ensembl:ENSG00000136807 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127789376..127789400 32194978 MeRIP-seq:(Medium) rs1339484627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16581305,Human_RBP_ID_22119373 107179 RMVar_ID_107179 Human_SNP_ID_415723978 m1A Human chr9 + 127789434 127789434 127789434 CATGCTCTCCACCCACCTGACGTCCATGTTCGAGTACTTGGCACCACCGCGCCGGAAGGGCAGCC CATGCTCTCCACCCACCTGACGTCCATGTTCGTGTACTTGGCACCACCGCGCCGGAAGGGCAGCC A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs760988808 Functional Loss SNV dbSNP153 33..33 33 - - - 107180 RMVar_ID_107180 Human_SNP_ID_415724002 m1A Human chr9 + 127789500 127789500 127789500 GATCACCCAGCAGTCCACCAACCAGAGTCGCAATCCCGCCACCACCAACCAGACGGAGTTTGAGC GATCACCCAGCAGTCCACCAACCAGAGTCGCAGTCCCGCCACCACCAACCAGACGGAGTTTGAGC A G CDK9 Ensembl:ENSG00000136807 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127789288..127789567 26863196 MeRIP-seq:(Medium) rs754937212 Functional Loss SNV dbSNP153 33..33 33 - - - 107181 RMVar_ID_107181 Human_SNP_ID_415724057 m1A Human chr9 - 127789584 127789584 127789584 GCCCTGTCTCCACGATGCAAGTCACATAGCAGAAGAAAAAAAACACAAGAGCCCTAGTGGCAAGC GCCCTGTCTCCACGATGCAAGTCACATAGCAGGAGAAAAAAAACACAAGAGCCCTAGTGGCAAGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127789536..127789787 32194978 MeRIP-seq:(Medium) rs746216061 Functional Loss SNV dbSNP153 33..33 33 - - - 107182 RMVar_ID_107182 Human_SNP_ID_415728210 m1A Human chr9 - 127803027 127803027 127803027 GTACTCCATGCTCGGCTCCTGCGGCACCGGCCACGCGCTCAAGCCCCGCCGCGCCGCGACCTGGG GTACTCCATGCTCGGCTCCTGCGGCACCGGCCGCGCGCTCAAGCCCCGCCGCGCCGCGACCTGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:127802926..127803094 26863410 MeRIP-seq:(Medium) rs1209352342 Functional Loss SNV dbSNP153 33..33 33 - - - 107183 RMVar_ID_107183 Human_SNP_ID_415728216 m1A Human chr9 + 127803040 127803040 127803040 GCGGCGGGGCTTGAGCGCGTGGCCGGTGCCGCAGGAGCCGAGCATGGAGTACCAGGTATCAGGCG GCGGCGGGGCTTGAGCGCGTGGCCGGTGCCGCGGGAGCCGAGCATGGAGTACCAGGTATCAGGCG A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr9:127802901..127803122;chr9:127802901..127803185;chr9:127802989..127803090 26863196,32194978 MeRIP-seq:(Medium) rs1184998322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037111 Human_Splice_Rec_1083337,Human_Splice_Rec_1083363,Human_Splice_Rec_1083389,Human_Splice_Rec_1083417,Human_Splice_Rec_1083437,Human_Splice_Rec_1083461,Human_Splice_Rec_1083469,Human_Splice_Rec_1083497 107184 RMVar_ID_107184 Human_SNP_ID_415728273 m1A Human chr9 + 127803159 127803159 127803159 CAGAACATCCGGGCTCCGCTAGCCGAGAGGGTATCGGGAGCCCTGGACTGGGGGACTCGGGGGGC CAGAACATCCGGGCTCCGCTAGCCGAGAGGGTGTCGGGAGCCCTGGACTGGGGGACTCGGGGGGC A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:127803143..127803317 26863196 MeRIP-seq:(Medium) rs1290177528 Functional Loss SNV dbSNP153 33..33 33 - - - 107185 RMVar_ID_107185 Human_SNP_ID_415728594 m1A Human chr9 - 127804362 127804362 127804362 AGGTACAGTTCCATGGCTTCCAACTGTGTCTGAGGGTCACCCCGCTGGCGCTTCACCTGCTCCAG AGGTACAGTTCCATGGCTTCCAACTGTGTCTGTGGGTCACCCCGCTGGCGCTTCACCTGCTCCAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127804253..127804510 26863196 MeRIP-seq:(Medium) rs1291410844 Functional Loss SNV dbSNP153 33..33 33 - - - 107186 RMVar_ID_107186 Human_SNP_ID_415729169 m1A Human chr9 - 127806656 127806656 127806656 TACCAATCAGTCACTCTGCTGACATCTGTCCCACAATGTCATCTGTCTTACAGCTCTCAGAGACA TACCAATCAGTCACTCTGCTGACATCTGTCCCGCAATGTCATCTGTCTTACAGCTCTCAGAGACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127806652..127806961 26863196 MeRIP-seq:(Medium) rs761966358 Functional Loss SNV dbSNP153 33..33 33 - - - 107187 RMVar_ID_107187 Human_SNP_ID_415729788 m1A Human chr9 - 127808619 127808619 127808619 CGTTGGACCGCTGGTGCTCCCCCTCCAGGCCCAGGGTCAGCGGCGGCCCCCCTTCCTCGAGGGCC CGTTGGACCGCTGGTGCTCCCCCTCCAGGCCCCGGGTCAGCGGCGGCCCCCCTTCCTCGAGGGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127808573..127808653 26863196 MeRIP-seq:(Medium) rs1374588715 Functional Loss SNV dbSNP153 33..33 33 - - - 107188 RMVar_ID_107188 Human_SNP_ID_415729837 m1A Human chr9 + 127808751 127808751 127808751 TGAGTGGGCAGGCAGGTGGGTGGCACCTGTGGAGCCTGCCTAGGAGGGTCCCGGACACACTTGGT TGAGTGGGCAGGCAGGTGGGTGGCACCTGTGGGGCCTGCCTAGGAGGGTCCCGGACACACTTGGT A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127808747..127808823 26863196 MeRIP-seq:(Medium) rs769402991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963814,Human_RBP_ID_5407931,Human_RBP_ID_19147592,Human_RBP_ID_22368178,Human_RBP_ID_22690254,Human_RBP_ID_26796545 RMVar_hsa_circ_10702,RMVar_hsa_circ_13664,RMVar_hsa_circ_266214 107189 RMVar_ID_107189 Human_SNP_ID_415730093 m1A Human chr9 - 127809621 127809621 127809621 GCCCTCTCCCACCCCCGTCCTCAATTCCGCACACACACTCCTGAGCCCGTTCTCCCCTGCAGGCT GCCCTCTCCCACCCCCGTCCTCAATTCCGCACGCACACTCCTGAGCCCGTTCTCCCCTGCAGGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127809578..127809680 26863196 MeRIP-seq:(Medium) rs1417559171 Functional Loss SNV dbSNP153 33..33 33 - - - 107190 RMVar_ID_107190 Human_SNP_ID_415730187 m1A Human chr9 + 127809824 127809810 127809825 GCTGGTTCCGCCAGGCGCTGCAGGGCCGCGAGAGGCCGAGCGGGTGAGGGGCAGGGCTGGGGGTG GCTGGTTCCGCCAGGCGCT_______________GCCGAGCGGGTGAGGGGCAGGGCTGGGGGTG TGCAGGGCCGCGAGAG T FPGS Ensembl:ENSG00000136877 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127809776..127810036 32194978 MeRIP-seq:(Medium) rs1409377836 Functional Loss DEL dbSNP153 20..34 33 - - - Human_Splice_Rec_1083357,Human_Splice_Rec_1083383,Human_Splice_Rec_1083411,Human_Splice_Rec_1083457,Human_Splice_Rec_1083491,Human_Splice_Rec_1083543,Human_Splice_Rec_1083605,Human_Splice_Rec_1083615,Human_Splice_Rec_1083623,Human_Splice_Rec_1083633 RMVar_hsa_circ_10702,RMVar_hsa_circ_13664,RMVar_hsa_circ_266214 107191 RMVar_ID_107191 Human_SNP_ID_415732141 m1A Human chr9 - 127815699 127815699 127815699 GCATCGGGAGCACCCAGAGCACCCCCTGCTCCACCAGCAGCATGGCATAGCCCCGGCCCCCCGCG GCATCGGGAGCACCCAGAGCACCCCCTGCTCCCCCAGCAGCATGGCATAGCCCCGGCCCCCCGCG T G ENG Ensembl:ENSG00000106991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127815442..127815801 26863196 MeRIP-seq:(Medium) rs1023446491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_274227,Human_miRNA_ID_2051491 RMVar_hsa_circ_103576,RMVar_hsa_circ_259811,RMVar_hsa_circ_92630,RMVar_hsa_circ_259810 107192 RMVar_ID_107192 Human_SNP_ID_415733173 m1A Human chr9 + 127818825 127818825 127818825 GGAAAGAGAGGCTGTCCATGTTGAGGCAGTGCACCTTTTTCTGGGGGAGGACGGGAGGGAGACTT GGAAAGAGAGGCTGTCCATGTTGAGGCAGTGCCCCTTTTTCTGGGGGAGGACGGGAGGGAGACTT A C AL162586.1 Ensembl:ENSG00000225032 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127818367..127819260 32194978 MeRIP-seq:(Medium) rs1554809363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5636371 Clinvar_Rec_686,Clinvar_Rec_13580 107193 RMVar_ID_107193 Human_SNP_ID_415734815 m1A Human chr9 - 127824355 127824355 127824355 AGCCCGGAGCTGCTCATGTCCTTGATCCAGACAAAGTGTGCCGACGACGCCATGACCCTGGTACT AGCCCGGAGCTGCTCATGTCCTTGATCCAGACCAAGTGTGCCGACGACGCCATGACCCTGGTACT T G ENG Ensembl:ENSG00000106991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127824279..127824389 26863196 MeRIP-seq:(Medium) rs746450444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1083652,Human_Splice_Rec_1083653,Human_Splice_Rec_1083680,Human_Splice_Rec_1083681,Human_Splice_Rec_1083708,Human_Splice_Rec_1083709,Human_Splice_Rec_1083721 RMVar_hsa_circ_82199,RMVar_hsa_circ_259811,RMVar_hsa_circ_92630,RMVar_hsa_circ_259812,RMVar_hsa_circ_38792,RMVar_hsa_circ_317659 107194 RMVar_ID_107194 Human_SNP_ID_415735724 m1A Human chr9 + 127826620 127826620 127826620 ACTCAAGGATCTGGGTCTTGGGGAAGGATGGCAGCTCTGTGGTGTTGACCCCCGGGGGCTCTTGG ACTCAAGGATCTGGGTCTTGGGGAAGGATGGCGGCTCTGTGGTGTTGACCCCCGGGGGCTCTTGG A G RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:127826571..127826708;chr9:127826571..127826703 26863196 MeRIP-seq:(Medium) rs546637270 Functional Loss SNV dbSNP153 33..33 33 - - - 107195 RMVar_ID_107195 Human_SNP_ID_415736508 m1A Human chr9 - 127829737 127829737 127829737 GAGAGGTGCTTCTGGTCCTCAGTGTAAACAGCAGTGTCTTCCTGCATCTCCAGGCCCTGGGAATC GAGAGGTGCTTCTGGTCCTCAGTGTAAACAGCGGTGTCTTCCTGCATCTCCAGGCCCTGGGAATC T C ENG Ensembl:ENSG00000106991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127829640..127829788 26863196 MeRIP-seq:(Medium) rs757343854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1083642,Human_Splice_Rec_1083643,Human_Splice_Rec_1083670,Human_Splice_Rec_1083671,Human_Splice_Rec_1083698,Human_Splice_Rec_1083699,Human_Splice_Rec_1083725 Human_miRNA_ID_1984646,Human_miRNA_ID_1984647,Human_miRNA_ID_3057452,Human_miRNA_ID_3057453 Clinvar_Rec_687 RMVar_hsa_circ_82199,RMVar_hsa_circ_259811,RMVar_hsa_circ_92630,RMVar_hsa_circ_259812,RMVar_hsa_circ_38792 107196 RMVar_ID_107196 Human_SNP_ID_415739992 m1A Human chr9 + 127843225 127843225 127843225 GCCCCTCTCGGGGCCCACAGGCTGAAGGTCACAATGGACTGTTTCTGCAAGACCTGTTGGAGAAA GCCCCTCTCGGGGCCCACAGGCTGAAGGTCACTATGGACTGTTTCTGCAAGACCTGTTGGAGAAA A T RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:127843201..127843225 26863196 MeRIP-seq:(Medium) rs1564462834 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_688 107197 RMVar_ID_107197 Human_SNP_ID_415742828 m1A Human chr9 + 127854422 127854422 127854422 TCCTGTGTCCAGTGGCAGGGCTGCGGGCGGGCACCGGGGCCGGCGTGGGCTCGCACGGGGACCCG TCCTGTGTCCAGTGGCAGGGCTGCGGGCGGGCCCCGGGGCCGGCGTGGGCTCGCACGGGGACCCG A C RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:127854276..127854700 26863196 MeRIP-seq:(Medium) rs1230303133 Functional Loss SNV dbSNP153 33..33 33 - - - 107198 RMVar_ID_107198 Human_SNP_ID_415742868 m1A Human chr9 + 127854534 127854534 127854534 GGGTGGCGGCCGAGGGGTCAGGAGAAGTGGACACAGGGACGCGGGGCTGGGCTGGAGTTGCTGTC GGGTGGCGGCCGAGGGGTCAGGAGAAGTGGACGCAGGGACGCGGGGCTGGGCTGGAGTTGCTGTC A G RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127854326..127854700 26863196 MeRIP-seq:(Medium) rs1420916372 Functional Loss SNV dbSNP153 33..33 33 - - - 107199 RMVar_ID_107199 Human_SNP_ID_415746424 m1A Human chr9 + 127868336 127868336 127868336 GGGCCCGCGGGGCCCACCTTGCGCACAATGCCACGTTTCTCATAGAAGGCGATGACAGGTTCTGT GGGCCCGCGGGGCCCACCTTGCGCACAATGCCGCGTTTCTCATAGAAGGCGATGACAGGTTCTGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127868326..127868350 26863196 MeRIP-seq:(Medium) rs760235278 Functional Loss SNV dbSNP153 33..33 33 - - - 107200 RMVar_ID_107200 Human_SNP_ID_415746453 m1A Human chr9 - 127868394 127868394 127868394 GCGTGTGGACGACAATGAGGAGACCATCAAAAAGCGGCTGGAGACCTATTACAAGGCCACAGAAC GCGTGTGGACGACAATGAGGAGACCATCAAAATGCGGCTGGAGACCTATTACAAGGCCACAGAAC T A AL157935.3,AK1 Ensembl:ENSG00000257524,Ensembl:ENSG00000106992 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127867901..127868547 26863196 MeRIP-seq:(Medium) rs1436130834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712283,Human_RBP_ID_26834297 Human_Splice_Rec_1083755,Human_Splice_Rec_1083760,Human_Splice_Rec_1083761,Human_Splice_Rec_1083767,Human_Splice_Rec_1083779,Human_Splice_Rec_1083789,Human_Splice_Rec_1083825,Human_Splice_Rec_1083849,Human_Splice_Rec_1083873,Human_Splice_Rec_1083887,Human_Splice_Rec_1083915 RMVar_hsa_circ_33583 107201 RMVar_ID_107201 Human_SNP_ID_415747448 m1A Human chr9 + 127871804 127871804 127871804 GTCTTATCCTGCCCCAGCCCACCAGGATCCCCACTTGGGTCAGTGCCTTACCCGTCGCTCAAACT GTCTTATCCTGCCCCAGCCCACCAGGATCCCCGCTTGGGTCAGTGCCTTACCCGTCGCTCAAACT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127871801..127871850 26863196 MeRIP-seq:(Medium) rs1451789288 Functional Loss SNV dbSNP153 33..33 33 - - - 107202 RMVar_ID_107202 Human_SNP_ID_415747708 m1A Human chr9 + 127872677 127872677 127872677 GGCTACTGTCATCCCCTGCCTCTCACCCCACCAGGGCCCACTCACCAGTGGAACCAGCTGCCCCT GGCTACTGTCATCCCCTGCCTCTCACCCCACCGGGGCCCACTCACCAGTGGAACCAGCTGCCCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127872676..127872700 26863196 MeRIP-seq:(Medium) rs1296547982 Functional Loss SNV dbSNP153 33..33 33 - - - 107203 RMVar_ID_107203 Human_SNP_ID_415747773 m1A Human chr9 - 127872840 127872840 127872840 AATGGGTGGGCGTTTGCAGGTGGGCCTGGCTCAGGGAAGGGCACCCAGTGTGAGAAGATCGTGCA AATGGGTGGGCGTTTGCAGGTGGGCCTGGCTCGGGGAAGGGCACCCAGTGTGAGAAGATCGTGCA T C AL157935.3,AK1 Ensembl:ENSG00000257524,Ensembl:ENSG00000106992 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127872676..127872894 26863196 MeRIP-seq:(Medium) rs758239561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974811,Human_RBP_ID_5010408,Human_RBP_ID_9339066,Human_RBP_ID_19025642,Human_RBP_ID_22556228,Human_RBP_ID_22690255 Human_Splice_Rec_1083750,Human_Splice_Rec_1083774,Human_Splice_Rec_1083784,Human_Splice_Rec_1083796,Human_Splice_Rec_1083820,Human_Splice_Rec_1083844,Human_Splice_Rec_1083868,Human_Splice_Rec_1083882,Human_Splice_Rec_1083910,Human_Splice_Rec_1083922,Human_Splice_Rec_1083932 RMVar_hsa_circ_33583 107204 RMVar_ID_107204 Human_SNP_ID_415751206 m1A Human chr9 - 127885422 127885422 127885422 TGTGAGGCTGGAGGGACCAGATGGAGGAGGCCAGCAGCTAGCCATTGCACACTGGGGTGATGGGT TGTGAGGCTGGAGGGACCAGATGGAGGAGGCCGGCAGCTAGCCATTGCACACTGGGGTGATGGGT T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:127885373..127885470;chr9:127885374..127885459 26863196 MeRIP-seq:(Medium) rs1317106554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712290,Human_RBP_ID_798338,Human_RBP_ID_5124182,Human_RBP_ID_5154464,Human_RBP_ID_22690835 107205 RMVar_ID_107205 Human_SNP_ID_415751804 m1A Human chr9 + 127887544 127887544 127887544 AGACATGCACGTGGTCACACAACTCCACCGCGATCACCATGGTAAACCAGCCTGTGCTCAACCAC AGACATGCACGTGGTCACACAACTCCACCGCGGTCACCATGGTAAACCAGCCTGTGCTCAACCAC A G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127886312..127890648 32194978 MeRIP-seq:(Medium) rs1269201886 Functional Loss SNV dbSNP153 33..33 33 - - - 107206 RMVar_ID_107206 Human_SNP_ID_415754416 m1A Human chr9 - 127897918 127897918 127897918 TGGTGAAACCGGGATTCGCACTGGCAGCTGACATGCTGTACTGACCATGGCCTTCTCAGAGCAGG TGGTGAAACCGGGATTCGCACTGGCAGCTGACGTGCTGTACTGACCATGGCCTTCTCAGAGCAGG T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:127897915..127898066 26863410 MeRIP-seq:(Medium) rs369667576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1083890,Human_Splice_Rec_1083952,Human_Splice_Rec_1083984,Human_Splice_Rec_1084006,Human_Splice_Rec_1084040,Human_Splice_Rec_1084048,Human_Splice_Rec_1084054,Human_Splice_Rec_1084055,Human_Splice_Rec_1084060,Human_Splice_Rec_1084061 107207 RMVar_ID_107207 Human_SNP_ID_415754456 m1A Human chr9 - 127898004 127898004 127898004 CGACTCTTATTGTTCCCATTTCACAGATGAGGAAACTGAGGCTCAGAGAGGTCACATGGCTTGCT CGACTCTTATTGTTCCCATTTCACAGATGAGGGAACTGAGGCTCAGAGAGGTCACATGGCTTGCT T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127897825..127898060 26863196 MeRIP-seq:(Medium) rs200910395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16581720 Human_Splice_Rec_1083890,Human_Splice_Rec_1083891,Human_Splice_Rec_1083941,Human_Splice_Rec_1083952,Human_Splice_Rec_1083953,Human_Splice_Rec_1083984,Human_Splice_Rec_1083985,Human_Splice_Rec_1084006,Human_Splice_Rec_1084007,Human_Splice_Rec_1084040,Human_Splice_Rec_1084041,Human_Splice_Rec_1084048,Human_Splice_Rec_1084049,Human_Splice_Rec_1084054,Human_Splice_Rec_1084060 107208 RMVar_ID_107208 Human_SNP_ID_415754688 m1A Human chr9 + 127898911 127898911 127898911 GGGGAGCGGCTTGCTCACGCTGGGGAGGCGGCAGCCCCGAGCGCTGGGCCAGGAGCATGGACTCA GGGGAGCGGCTTGCTCACGCTGGGGAGGCGGCCGCCCCGAGCGCTGGGCCAGGAGCATGGACTCA A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127898904..127899066 32194978 MeRIP-seq:(Medium) rs569431080 Functional Loss SNV dbSNP153 33..33 33 - - - 107209 RMVar_ID_107209 Human_SNP_ID_415754844 m1A Human chr9 + 127899448 127899448 127899448 TAGCAATCTCCTCTCCCGGCGCCCTCCGCCCCAGCCCCCGCCTCCGCCCCCGCCCCCGCGGCCTG TAGCAATCTCCTCTCCCGGCGCCCTCCGCCCCCGCCCCCGCCTCCGCCCCCGCCCCCGCGGCCTG A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:127899445..127899600 26863410 MeRIP-seq:(Medium) rs1243296612 Functional Loss SNV dbSNP153 33..33 33 - - - 107210 RMVar_ID_107210 Human_SNP_ID_415754850 m1A Human chr9 - 127899458 127899458 127899458 CGCGCGGGAGCAGGCCGCGGGGGCGGGGGCGGAGGCGGGGGCTGGGGCGGAGGGCGCCGGGAGAG CGCGCGGGAGCAGGCCGCGGGGGCGGGGGCGGGGGCGGGGGCTGGGGCGGAGGGCGCCGGGAGAG T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127899454..127899596 26863196 MeRIP-seq:(Medium) rs1193339020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5408691,Human_RBP_ID_8223401,Human_RBP_ID_26796550 107211 RMVar_ID_107211 Human_SNP_ID_415759758 m1A Human chr9 + 127916493 127916493 127916493 GGGCTGGGGCTGGGAAGGGGTGGGAGCCGGGCACCTGCCAAGACCCAGAAACTCAGAGCCGGGAG GGGCTGGGGCTGGGAAGGGGTGGGAGCCGGGCCCCTGCCAAGACCCAGAAACTCAGAGCCGGGAG A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127916458..127916998 26863196 MeRIP-seq:(Medium) rs375089890 Functional Loss SNV dbSNP153 33..33 33 - - - 107212 RMVar_ID_107212 Human_SNP_ID_415759834 m1A Human chr9 - 127916846 127916846 127916846 AAACCTACGTCCTGCCCTCGCCCGGCCTCTCCATTCGTCCCCCGGGTAGAGAGGTAGGATGGATG AAACCTACGTCCTGCCCTCGCCCGGCCTCTCCGTTCGTCCCCCGGGTAGAGAGGTAGGATGGATG T C ST6GALNAC4 Ensembl:ENSG00000136840 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127916408..127916939 32194978 MeRIP-seq:(Medium) rs1210907054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037119,Human_RBP_ID_5515669 Human_Splice_Rec_1084063,Human_Splice_Rec_1084081,Human_Splice_Rec_1084089,Human_Splice_Rec_1084099 RMVar_hsa_circ_108756,RMVar_hsa_circ_259821,RMVar_hsa_circ_88871,RMVar_hsa_circ_259822 107213 RMVar_ID_107213 Human_SNP_ID_415761869 m1A Human chr9 - 127924843 127924843 127924843 GTAGAGGGGAGGGCTGGAGAAGCCTGGCTGGTAGGGCAGGAGGGGCACAGGTGGACTGCAGCAGG GTAGAGGGGAGGGCTGGAGAAGCCTGGCTGGTGGGGCAGGAGGGGCACAGGTGGACTGCAGCAGG T C PIP5KL1 Ensembl:ENSG00000167103 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127924841..127924921 26863196 MeRIP-seq:(Medium) rs544706006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5658607 107214 RMVar_ID_107214 Human_SNP_ID_415761872 m1A Human chr9 + 127924861 127924861 127924861 TGCCCCTCCTGCCCTACCAGCCAGGCTTCTCCAGCCCTCCCCTCTACACACACACACACGCACAC TGCCCCTCCTGCCCTACCAGCCAGGCTTCTCCCGCCCTCCCCTCTACACACACACACACGCACAC A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127924814..127924955 26863196 MeRIP-seq:(Medium) rs1415836465 Functional Loss SNV dbSNP153 33..33 33 - - - 107215 RMVar_ID_107215 Human_SNP_ID_415762330 m1A Human chr9 - 127926169 127926166 127926170 GGGAAAGAAAGAGAGAAGAGAGAGAAAGAAAGAAAAGAGAGAGAGAAAGAAAGAAAAGAGAGAAA GGGAAAGAAAGAGAGAAGAGAGAGAAAGAAA____AGAGAGAGAGAAAGAAAGAAAAGAGAGAAA TTTTC T PIP5KL1 Ensembl:ENSG00000167103 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127926119..127926222 26863196 MeRIP-seq:(Medium) rs201063633 Functional Loss DEL dbSNP153 32..35 33 - - - 107216 RMVar_ID_107216 Human_SNP_ID_415762842 m1A Human chr9 + 127927825 127927825 127927825 GTCACTGCCCAGGCCTGGCTGGAGCGGCTCCCACCCGGCCCCCTTCCCCGACCTGTGCACGTGGA GTCACTGCCCAGGCCTGGCTGGAGCGGCTCCCCCCCGGCCCCCTTCCCCGACCTGTGCACGTGGA A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127927815..127927934 26863196 MeRIP-seq:(Medium) rs899589008 Functional Loss SNV dbSNP153 33..33 33 - - - 107217 RMVar_ID_107217 Human_SNP_ID_415763888 m1A Human chr9 - 127931529 127931529 127931529 GGAGTCTGGCAAGGTGACGAAAGAACGAGGCGAGTAGCAGTCTGGGGTCAAGAGTTTCAAGCAGA GGAGTCTGGCAAGGTGACGAAAGAACGAGGCGTGTAGCAGTCTGGGGTCAAGAGTTTCAAGCAGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127931390..127931631 26863196 MeRIP-seq:(Medium) rs200797488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900284,Human_RBP_ID_16581783 107218 RMVar_ID_107218 Human_SNP_ID_415764918 m1A Human chr9 + 127935329 127935329 127935329 CAGGGTAAGGAAAGCTGCCTTGGTGGAGGAAGAGAAGTCAGAGAGGTCACACATGTGGCCTTAGA CAGGGTAAGGAAAGCTGCCTTGGTGGAGGAAGGGAAGTCAGAGAGGTCACACATGTGGCCTTAGA A G AL157935.2 Ensembl:ENSG00000227218 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:127935251..127935350 26863196 MeRIP-seq:(Medium) rs141613457 Functional Loss SNV dbSNP153 33..33 33 - - - 107219 RMVar_ID_107219 Human_SNP_ID_415764944 m1A Human chr9 - 127935452 127935448 127935452 AGGGCCTAAAAGATGCTGGTCCTCCCAACCTCACTCTCAGACTCCCTGCCACCTTTTCCCCTGGG AGGGCCTAAAAGATGCTGGTCCTCCCAACCTC____TCAGACTCCCTGCCACCTTTTCCCCTGGG AGAGT A DPM2 Ensembl:ENSG00000136908 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127935401..127936048 32194978 MeRIP-seq:(Medium) rs1451660359 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_712340,Human_RBP_ID_17323625,Human_RBP_ID_17437348,Human_RBP_ID_17715909,Human_RBP_ID_18130124,Human_RBP_ID_18962315,Human_RBP_ID_21658728,Human_RBP_ID_26560966,Human_RBP_ID_27542334 Human_miRNA_ID_191758 107220 RMVar_ID_107220 Human_SNP_ID_415765170 m1A Human chr9 - 127936348 127936348 127936348 CCCCAGGCTTTTTGGACTCCAATGACCTGTCTACCTCTTTCCTGCCCCAACCCCATCATCACTCT CCCCAGGCTTTTTGGACTCCAATGACCTGTCTTCCTCTTTCCTGCCCCAACCCCATCATCACTCT T A DPM2 Ensembl:ENSG00000136908 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127936345..127936446 32194978 MeRIP-seq:(Medium) rs764816592 Functional Loss SNV dbSNP153 33..33 33 - - - 107221 RMVar_ID_107221 Human_SNP_ID_415765171 m1A Human chr9 - 127936348 127936348 127936348 CCCCAGGCTTTTTGGACTCCAATGACCTGTCTACCTCTTTCCTGCCCCAACCCCATCATCACTCT CCCCAGGCTTTTTGGACTCCAATGACCTGTCTGCCTCTTTCCTGCCCCAACCCCATCATCACTCT T C DPM2 Ensembl:ENSG00000136908 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127936345..127936446 32194978 MeRIP-seq:(Medium) rs764816592 Functional Loss SNV dbSNP153 33..33 33 - - - 107222 RMVar_ID_107222 Human_SNP_ID_415765211 m1A Human chr9 - 127936448 127936448 127936448 ACTTTGGCGGTGCTGGAAGCTGCTTGCCCCGAACTCACCCGTGGGGTTTTCCTGTTCATCCTTCG ACTTTGGCGGTGCTGGAAGCTGCTTGCCCCGAGCTCACCCGTGGGGTTTTCCTGTTCATCCTTCG T C DPM2 Ensembl:ENSG00000136908 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127936445..127936744 32194978 MeRIP-seq:(Medium) rs1352539802 Functional Loss SNV dbSNP153 33..33 33 - - - 107223 RMVar_ID_107223 Human_SNP_ID_415765284 m1A Human chr9 - 127936627 127936627 127936627 CCAGCCATTCATCGACAGTCAGCATGTCATCCACAAGTATTTCCTGCCCCGAGCCTATGCTGTCG CCAGCCATTCATCGACAGTCAGCATGTCATCCGCAAGTATTTCCTGCCCCGAGCCTATGCTGTCG T C DPM2 Ensembl:ENSG00000136908 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127936576..127936675 26863196 MeRIP-seq:(Medium) rs778216191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961570,Human_RBP_ID_1337937,Human_RBP_ID_19145880,Human_RBP_ID_26833577 Human_Splice_Rec_1084235,Human_Splice_Rec_1084240,Human_Splice_Rec_1084241,Human_Splice_Rec_1084244,Human_Splice_Rec_1084245,Human_Splice_Rec_1084252 RMVar_hsa_circ_259828,RMVar_hsa_circ_373847 107224 RMVar_ID_107224 Human_SNP_ID_415765458 m1A Human chr9 - 127937369 127937369 127937369 CCCCGAGCCCTGGCACCGCCAGAGCAACTACTATATAGGCTCTAGGCACGGCGCTGGCTTCATTG CCCCGAGCCCTGGCACCGCCAGAGCAACTACTGTATAGGCTCTAGGCACGGCGCTGGCTTCATTG T C DPM2 Ensembl:ENSG00000136908 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127937340..127937440 32194978 MeRIP-seq:(Medium) rs1430409084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21689365 RMVar_hsa_circ_259828,RMVar_hsa_circ_373847 107225 RMVar_ID_107225 Human_SNP_ID_415765518 m1A Human chr9 + 127937501 127937501 127937501 TGATCAGGCTAACGGCGACGAGGCCGAGTCCCACCACCTGGTCTGTCCCCGTGGCCTGGAGAAAA TGATCAGGCTAACGGCGACGAGGCCGAGTCCCGCCACCTGGTCTGTCCCCGTGGCCTGGAGAAAA A G AL157935.2 Ensembl:ENSG00000227218 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127937396..127937525;chr9:127937426..127937525 26863196 MeRIP-seq:(Medium) rs923922683 Functional Loss SNV dbSNP153 33..33 33 - - - 107226 RMVar_ID_107226 Human_SNP_ID_415765573 m1A Human chr9 - 127937700 127937700 127937700 AACGGGGATTGCTCTCCCGCCCCCACTATTGTACGGACGACAACGCGGAGGCCTAGCATTCTCTC AACGGGGATTGCTCTCCCGCCCCCACTATTGTCCGGACGACAACGCGGAGGCCTAGCATTCTCTC T G DPM2 Ensembl:ENSG00000136908 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127937685..127937850 26863196 MeRIP-seq:(Medium) rs958069659 Functional Loss SNV dbSNP153 33..33 33 - - - 107227 RMVar_ID_107227 Human_SNP_ID_415765584 m1A Human chr9 + 127937720 127937720 127937720 CGTTGTCGTCCGTACAATAGTGGGGGCGGGAGAGCAATCCCCGTTCCAAGTGCCCATGCCCCAGC CGTTGTCGTCCGTACAATAGTGGGGGCGGGAGGGCAATCCCCGTTCCAAGTGCCCATGCCCCAGC A G AL157935.2 Ensembl:ENSG00000227218 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127937710..127937834 26863196 MeRIP-seq:(Medium) rs1469464881 Functional Loss SNV dbSNP153 33..33 33 - - - 107228 RMVar_ID_107228 Human_SNP_ID_415766888 m1A Human chr9 + 127942508 127942508 127942508 CCAGTGGGACTGTGCTGGGGGTGAGCATGTGCAAAGTGCAGGCTGCAAGGCAGCGGGAGGACATT CCAGTGGGACTGTGCTGGGGGTGAGCATGTGCGAAGTGCAGGCTGCAAGGCAGCGGGAGGACATT A G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127942401..127942646 26863196 MeRIP-seq:(Medium) rs1227949799 Functional Loss SNV dbSNP153 33..33 33 - - - 107229 RMVar_ID_107229 Human_SNP_ID_415766915 m1A Human chr9 - 127942594 127942594 127942594 GGGGACCTGCTGGCGGCCTCTTCCTGGGAGCCATGACCTCAGACCCCACCCACACTCCAGATCGA GGGGACCTGCTGGCGGCCTCTTCCTGGGAGCCGTGACCTCAGACCCCACCCACACTCCAGATCGA T C FAM102A Ensembl:ENSG00000167106 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:127942576..127942600 26863196 MeRIP-seq:(Medium) rs1340229195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094726,Human_RBP_ID_18963095 Human_miRNA_ID_259750,Human_miRNA_ID_263545 107230 RMVar_ID_107230 Human_SNP_ID_415767078 m1A Human chr9 - 127943091 127943091 127943091 GAACTTTCCCCTTCAGATCACCTCTGCGCCACATCTCATCCATGCCTCCTCCATGCACTCCAGTC GAACTTTCCCCTTCAGATCACCTCTGCGCCACGTCTCATCCATGCCTCCTCCATGCACTCCAGTC T C FAM102A Ensembl:ENSG00000167106 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:127942991..127943175 26863196 MeRIP-seq:(Medium) rs528795656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18963097 Human_miRNA_ID_303578,Human_miRNA_ID_734978 107231 RMVar_ID_107231 Human_SNP_ID_415776623 m1A Human chr9 - 127980555 127980554 127980555 GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCCAGCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCC_GCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG CT C FAM102A Ensembl:ENSG00000167106 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:127980453..127980673 26863410 MeRIP-seq:(Medium) rs1424342557 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5454176 107232 RMVar_ID_107232 Human_SNP_ID_415776624 m1A Human chr9 - 127980555 127980555 127980555 GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCCAGCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCCCGCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG T G FAM102A Ensembl:ENSG00000167106 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:127980453..127980673 26863410 MeRIP-seq:(Medium) rs113481265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5454176 Clinvar_Rec_689 GWAS_ID_14726,GWAS_ID_14727,GWAS_ID_14728,GWAS_ID_14729 107233 RMVar_ID_107233 Human_SNP_ID_415798564 m1A Human chr9 + 128063861 128063861 128063861 GTGGGGGCGCCTCAGCCGTGCAGTACTCCACCACGCCCTCCTCCAGCGTGTGATAGGTGGTCTCT GTGGGGGCGCCTCAGCCGTGCAGTACTCCACCGCGCCCTCCTCCAGCGTGTGATAGGTGGTCTCT A G RF00017-4572,RF00017-1264,RF00017-4498,lnc-SLC25A25-4 RNACentral:URS000099187D,RNACentral:URS00009A773B,RNACentral:URS0000930330,RNACentral:URS0000D5B816 SRP RNA,SRP RNA,SRP RNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128063811..128066206 26863196 MeRIP-seq:(Medium) rs1479737056 Functional Loss SNV dbSNP153 33..33 33 - - - 107234 RMVar_ID_107234 Human_SNP_ID_415798570 m1A Human chr9 + 128063873 128063873 128063873 CAGCCGTGCAGTACTCCACCACGCCCTCCTCCAGCGTGTGATAGGTGGTCTCTGTGGGGACTGCA CAGCCGTGCAGTACTCCACCACGCCCTCCTCCGGCGTGTGATAGGTGGTCTCTGTGGGGACTGCA A G RF00017-4572,RF00017-1264,RF00017-4498,lnc-SLC25A25-4 RNACentral:URS000099187D,RNACentral:URS00009A773B,RNACentral:URS0000930330,RNACentral:URS0000D5B816 SRP RNA,SRP RNA,SRP RNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128063823..128063947 26863196 MeRIP-seq:(Medium) rs751191974 Functional Loss SNV dbSNP153 33..33 33 - - - 107235 RMVar_ID_107235 Human_SNP_ID_415799904 m1A Human chr9 + 128068263 128068263 128068263 TGCAGAGCGCCTGGCTTGCCTCCCGCGCGGTCACCGCCGGCCCGCCGCCCCCGCTCCCGCCCGCG TGCAGAGCGCCTGGCTTGCCTCCCGCGCGGTCGCCGCCGGCCCGCCGCCCCCGCTCCCGCCCGCG A G SLC25A25 Ensembl:ENSG00000148339 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128068228..128068382 26863196 MeRIP-seq:(Medium) rs978689726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036434,Human_RBP_ID_8930630 107236 RMVar_ID_107236 Human_SNP_ID_415799908 m1A Human chr9 - 128068285 128068274 128068286 GGCGCGAGGCAGGGGCTCCGGGCGCGGGCGGGAGCGGGGGCGGCGGGCCGGCGGTGACCGCGCGG GGCGCGAGGCAGGGGCTCCGGGCGCGGGCGG____________CGGGCCGGCGGTGACCGCGCGG GCCGCCCCCGCTC G RF00017-4525,L13304-001,L13705-009 RNACentral:URS00009368C0,RNACentral:URS000044B5AA,RNACentral:URS00001E2917 SRP RNA,scRNA,misc_RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128068234..128068527 26863196 MeRIP-seq:(Medium) rs1564174412 Functional Loss DEL dbSNP153 32..43 33 - - - 107237 RMVar_ID_107237 Human_SNP_ID_415799949 m1A Human chr9 + 128068366 128068356 128068366 GTTGTGCCGCTGTGTGGCCTCCCCGCCGCCGGACGCCGCCGCCACCGCCGCCTCTTCGTCTGCCT GTTGTGCCGCTGTGTGGCCTCCC__________CGCCGCCGCCACCGCCGCCTCTTCGTCTGCCT CCGCCGCCGGA C SLC25A25 Ensembl:ENSG00000148339 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128068229..128068406 26863196 MeRIP-seq:(Medium) rs757574236 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_5037122,Human_RBP_ID_9315184,Human_RBP_ID_9339068 107238 RMVar_ID_107238 Human_SNP_ID_415807499 m1A Human chr9 - 128098595 128098595 128098595 AGTACTGGAACTCGGTCTGGGCTTCCCCGATGACCGGCACATACAGGCACAGACAGAGCATGTTG AGTACTGGAACTCGGTCTGGGCTTCCCCGATGGCCGGCACATACAGGCACAGACAGAGCATGTTG T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128098593..128098694 32194978 MeRIP-seq:(Medium) rs767712754 Functional Loss SNV dbSNP153 33..33 33 - - - 107239 RMVar_ID_107239 Human_SNP_ID_415808192 m1A Human chr9 - 128101204 128101204 128101204 AAGGCAACACTTACCATCATTCTTTTTGTCCAAACTCTTAAACACCAGCCTCAGCTTCTTCTCAT AAGGCAACACTTACCATCATTCTTTTTGTCCAGACTCTTAAACACCAGCCTCAGCTTCTTCTCAT T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128101157..128101240 26863196 MeRIP-seq:(Medium) rs1352997814 Functional Loss SNV dbSNP153 33..33 33 - - - 107240 RMVar_ID_107240 Human_SNP_ID_415809514 m1A Human chr9 + 128105774 128105774 128105774 GCAGCAACAACATGGGCATCGTTGGTGGCTTCACTCAGATGATTCGAGAAGGAGGGGCCAGGTCA GCAGCAACAACATGGGCATCGTTGGTGGCTTCGCTCAGATGATTCGAGAAGGAGGGGCCAGGTCA A G SLC25A25 Ensembl:ENSG00000148339 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128102444..128106444 32194978 MeRIP-seq:(Medium) rs755086874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962667 Human_Splice_Rec_1084336,Human_Splice_Rec_1084356,Human_Splice_Rec_1084376,Human_Splice_Rec_1084394,Human_Splice_Rec_1084412 RMVar_hsa_circ_781,RMVar_hsa_circ_54101,RMVar_hsa_circ_283668,RMVar_hsa_circ_39968,RMVar_hsa_circ_259833,RMVar_hsa_circ_361872,RMVar_hsa_circ_259834,RMVar_hsa_circ_375950 107241 RMVar_ID_107241 Human_SNP_ID_415810316 m1A Human chr9 - 128108275 128108275 128108275 TAAGGCCTCCAACACCTTTTCCTTCCCTCCCCAGAACACACAAACGCTCTGCCCTTCGCCCTCAA TAAGGCCTCCAACACCTTTTCCTTCCCTCCCCGGAACACACAAACGCTCTGCCCTTCGCCCTCAA T C SLC25A25-AS1,SLC25A25-AS1:2,SLC25A25-AS1:3,SLC25A25-AS1:4,L13304-001,L13705-009 RNACentral:URS0000D6E07B,RNACentral:URS00008C3178,RNACentral:URS0000D6D77D,RNACentral:URS00008C1F31,RNACentral:URS000044B5AA,RNACentral:URS00001E2917 lincRNA,lincRNA,lincRNA,lincRNA,scRNA,misc_RNA exon,exon,intron,exon,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128108226..128108358;chr9:128108228..128108312 26863196 MeRIP-seq:(Medium) rs935616673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1247712 107242 RMVar_ID_107242 Human_SNP_ID_415813045 m1A Human chr9 + 128118597 128118597 128118597 GGATGCTGGGATGGAGGATGGAGGGCACAGGGATACAGGAATGGAGGGATGGAAAAATAGAGGGA GGATGCTGGGATGGAGGATGGAGGGCACAGGGTTACAGGAATGGAGGGATGGAAAAATAGAGGGA A T lnc-SLC25A25-2,lnc-SLC25A25-2:2 RNACentral:URS00008BC09F,RNACentral:URS00008BDFF7 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128118557..128118808 26863196 MeRIP-seq:(Medium) rs1564204782 Functional Loss SNV dbSNP153 33..33 33 - - - 107243 RMVar_ID_107243 Human_SNP_ID_415813322 m1A Human chr9 + 128119008 128119002 128119009 GGTACAGGGATGGAGGGGTGCAGGGATGGGGGACGGAGGGGTACAGGGATGGGGTACAGGGATGG GGTACAGGGATGGAGGGGTGCAGGGAT_______GGAGGGGTACAGGGATGGGGTACAGGGATGG TGGGGGAC T lnc-SLC25A25-2,lnc-SLC25A25-2:2 RNACentral:URS00008BC09F,RNACentral:URS00008BDFF7 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128118958..128119060 26863196 MeRIP-seq:(Medium) rs1380734901 Functional Loss DEL dbSNP153 28..34 33 - - - 107244 RMVar_ID_107244 Human_SNP_ID_415813332 m1A Human chr9 + 128119008 128119008 128119008 GGTACAGGGATGGAGGGGTGCAGGGATGGGGGACGGAGGGGTACAGGGATGGGGTACAGGGATGG GGTACAGGGATGGAGGGGTGCAGGGATGGGGGGCGGAGGGGTACAGGGATGGGGTACAGGGATGG A G lnc-SLC25A25-2,lnc-SLC25A25-2:2 RNACentral:URS00008BC09F,RNACentral:URS00008BDFF7 lincRNA,lincRNA exon,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128118958..128119060 26863196 MeRIP-seq:(Medium) rs1218691685 Functional Loss SNV dbSNP153 33..33 33 - - - 107245 RMVar_ID_107245 Human_SNP_ID_415814042 m1A Human chr9 - 128121249 128121249 128121249 TGCCCCAGGCGGTGTATGGCGTGCTGCGTGTGATGGAGGGGCTGGATGCGTTCGATGACCTGATG TGCCCCAGGCGGTGTATGGCGTGCTGCGTGTGGTGGAGGGGCTGGATGCGTTCGATGACCTGATG T C PTGES2 Ensembl:ENSG00000148334 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128120769..128121307 26863196 MeRIP-seq:(Medium) rs903979956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797059,Human_RBP_ID_17666820,Human_RBP_ID_22690276,Human_RBP_ID_22747794,Human_RBP_ID_24287359 Human_Splice_Rec_1084458,Human_Splice_Rec_1084470,Human_Splice_Rec_1084482,Human_Splice_Rec_1084494,Human_Splice_Rec_1084498,Human_Splice_Rec_1084506 RMVar_hsa_circ_81367,RMVar_hsa_circ_103542,RMVar_hsa_circ_97324,RMVar_hsa_circ_259840,RMVar_hsa_circ_259841,RMVar_hsa_circ_259842 107246 RMVar_ID_107246 Human_SNP_ID_415814734 m1A Human chr9 - 128123136 128123136 128123136 GTCCTGGCTTAGGAAGTCCCTCCCGTGCCCGCAGGGAGGAGATGAAGTGGCGGCAGTGGGCGGAC GTCCTGGCTTAGGAAGTCCCTCCCGTGCCCGCGGGGAGGAGATGAAGTGGCGGCAGTGGGCGGAC T C PTGES2 Ensembl:ENSG00000148334 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128123101..128123150;chr9:128123126..128123150 26863196 MeRIP-seq:(Medium) rs1357768430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22690277 RMVar_hsa_circ_103542,RMVar_hsa_circ_97324,RMVar_hsa_circ_259841,RMVar_hsa_circ_259842,RMVar_hsa_circ_303880,RMVar_hsa_circ_316467,RMVar_hsa_circ_93067,RMVar_hsa_circ_259844 107247 RMVar_ID_107247 Human_SNP_ID_415814942 m1A Human chr9 - 128123790 128123790 128123790 ACCCAGCCATGAAGGCTGTGAACGAGCAGGGCAAGGAGGTGACCGAGTTCGGCAATAAGTACTGG ACCCAGCCATGAAGGCTGTGAACGAGCAGGGCGAGGAGGTGACCGAGTTCGGCAATAAGTACTGG T C PTGES2 Ensembl:ENSG00000148334 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128123741..128124371 32194978 MeRIP-seq:(Medium) rs1184416124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633652,Human_RBP_ID_16582525,Human_RBP_ID_26361126 Human_Splice_Rec_1084454,Human_Splice_Rec_1084455,Human_Splice_Rec_1084466,Human_Splice_Rec_1084467,Human_Splice_Rec_1084478,Human_Splice_Rec_1084479,Human_Splice_Rec_1084490,Human_Splice_Rec_1084491,Human_Splice_Rec_1084495,Human_Splice_Rec_1084502,Human_Splice_Rec_1084503,Human_Splice_Rec_1084514,Human_Splice_Rec_1084515,Human_Splice_Rec_1084522,Human_Splice_Rec_1084523,Human_Splice_Rec_1084530,Human_Splice_Rec_1084531,Human_Splice_Rec_1084538,Human_Splice_Rec_1084539,Human_Splice_Rec_1084548,Human_Splice_Rec_1084549,Human_Splice_Rec_1084558,Human_Splice_Rec_1084559 Human_miRNA_ID_270390,Human_miRNA_ID_2015866,Human_miRNA_ID_2380712,Human_miRNA_ID_3023726,Human_miRNA_ID_3090409 RMVar_hsa_circ_103542,RMVar_hsa_circ_97324,RMVar_hsa_circ_259841,RMVar_hsa_circ_259842,RMVar_hsa_circ_303880,RMVar_hsa_circ_316467,RMVar_hsa_circ_93067,RMVar_hsa_circ_90116,RMVar_hsa_circ_259844,RMVar_hsa_circ_259845 107248 RMVar_ID_107248 Human_SNP_ID_415816259 m1A Human chr9 - 128127568 128127568 128127568 GGGGCGGCGGGCGGCCCGAGCCCCGTGGCTGCAGCTCGTAAGGGGAGCCCGCGGCTGCTGGGAGC GGGGCGGCGGGCGGCCCGAGCCCCGTGGCTGCGGCTCGTAAGGGGAGCCCGCGGCTGCTGGGAGC T C PTGES2 Ensembl:ENSG00000148334 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128127518..128127725 26863196 MeRIP-seq:(Medium) rs925796164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037123 RMVar_hsa_circ_103542,RMVar_hsa_circ_259842,RMVar_hsa_circ_93067,RMVar_hsa_circ_90116,RMVar_hsa_circ_259844,RMVar_hsa_circ_259845 107249 RMVar_ID_107249 Human_SNP_ID_415816311 m1A Human chr9 + 128127684 128127684 128127684 CAGCCTCCAGGCCAAGGCGCACCCACCAGGCCACAGCGCCCGCACCACCCGCGCAGCCGGGTCCA CAGCCTCCAGGCCAAGGCGCACCCACCAGGCCGCAGCGCCCGCACCACCCGCGCAGCCGGGTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128127397..128127725 26863196 MeRIP-seq:(Medium) rs1231061815 Functional Loss SNV dbSNP153 33..33 33 - - - 107250 RMVar_ID_107250 Human_SNP_ID_415816772 m1A Human chr9 - 128128358 128128358 128128358 AGCTAGGGCGGGGGAGCCCAGCAGAAGGACCGAGCAGCCTGGCACCCCACTTTGCCATCCTCTCC AGCTAGGGCGGGGGAGCCCAGCAGAAGGACCGCGCAGCCTGGCACCCCACTTTGCCATCCTCTCC T G PTGES2 Ensembl:ENSG00000148334 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128128312..128128379 26863196 MeRIP-seq:(Medium) rs764511521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18427223 RMVar_hsa_circ_103542,RMVar_hsa_circ_259842,RMVar_hsa_circ_93067,RMVar_hsa_circ_90116,RMVar_hsa_circ_259844,RMVar_hsa_circ_259845 107251 RMVar_ID_107251 Human_SNP_ID_415828712 m1A Human chr9 - 128163780 128163760 128163781 GGGCATGCCAGGTGGTGGGGGCTGGCCCAGGTAGGCCAAGGGGAGGCCCAGGCAGGAAGGGTGGC GGGCATGCCAGGTGGTGGGGGCTGGCCCAGG_____________________CAGGAAGGGTGGC GCCTGGGCCTCCCCTTGGCCTA G CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128163731..128163834 26863196 MeRIP-seq:(Medium) rs1384975613 Functional Loss DEL dbSNP153 32..52 33 - - - 107252 RMVar_ID_107252 Human_SNP_ID_415829335 m1A Human chr9 - 128166205 128166205 128166205 AGCCCCCACTACCTCGGCGCTCAACCCGCCTCAAAACCTGATAGAGGGACCTCCCTGTCCCTGGC AGCCCCCACTACCTCGGCGCTCAACCCGCCTCCAAACCTGATAGAGGGACCTCCCTGTCCCTGGC T G CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs551056588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712434,Human_RBP_ID_5124191,Human_RBP_ID_27542402 Human_miRNA_ID_2689759,Human_miRNA_ID_2955708 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 107253 RMVar_ID_107253 Human_SNP_ID_415829371 m1A Human chr9 - 128166276 128166276 128166276 CAGCGGCCGCCCACCCTCCCAGCCCAACACCCAGGACAAAACACCCAGCAAGGTGACGGCTCGAC CAGCGGCCGCCCACCCTCCCAGCCCAACACCCCGGACAAAACACCCAGCAAGGTGACGGCTCGAC T G CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr9:128166153..128166325;chr9:128166226..128166350 26863196 MeRIP-seq:(Medium) rs1376182147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17437215,Human_RBP_ID_26834320 Human_Splice_Rec_1084681 Human_miRNA_ID_255964,Human_miRNA_ID_656305,Human_miRNA_ID_2039888,Human_miRNA_ID_2254778,Human_miRNA_ID_3018869 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 107254 RMVar_ID_107254 Human_SNP_ID_415829431 m1A Human chr9 - 128166404 128166404 128166404 CCTGACCTTACCTGCACCTTCTGTATCCAGAAATACAAGGCGGCCAAGAACCCCAGCCCCACCAC CCTGACCTTACCTGCACCTTCTGTATCCAGAAGTACAAGGCGGCCAAGAACCCCAGCCCCACCAC T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128166203..128166436 26863196 MeRIP-seq:(Medium) rs1275358035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3975789,Human_RBP_ID_9339075,Human_RBP_ID_26362115 Human_Splice_Rec_1084680,Human_Splice_Rec_1084690,Human_Splice_Rec_1084694,Human_Splice_Rec_1084726,Human_Splice_Rec_1084758,Human_Splice_Rec_1084790,Human_Splice_Rec_1084824,Human_Splice_Rec_1084858,Human_Splice_Rec_1084864,Human_Splice_Rec_1084894,Human_Splice_Rec_1084926,Human_Splice_Rec_1084960,Human_Splice_Rec_1084998,Human_Splice_Rec_1085026,Human_Splice_Rec_1085042,Human_Splice_Rec_1085044 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 107255 RMVar_ID_107255 Human_SNP_ID_415829574 m1A Human chr9 + 128166877 128166877 128166877 AGATATAGCCCATCACGGGCACCAGGAAGTCCACACCTGTAGGATGGGATGGCAGGGTCTGCACT AGATATAGCCCATCACGGGCACCAGGAAGTCCTCACCTGTAGGATGGGATGGCAGGGTCTGCACT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128166732..128166900 26863196 MeRIP-seq:(Medium) rs15126 Functional Loss SNV dbSNP153 33..33 33 - - - 107256 RMVar_ID_107256 Human_SNP_ID_415829575 m1A Human chr9 + 128166879 128166879 128166879 ATATAGCCCATCACGGGCACCAGGAAGTCCACACCTGTAGGATGGGATGGCAGGGTCTGCACTCA ATATAGCCCATCACGGGCACCAGGAAGTCCACCCCTGTAGGATGGGATGGCAGGGTCTGCACTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128166876..128166900 26863196 MeRIP-seq:(Medium) rs374054563 Functional Loss SNV dbSNP153 33..33 33 - - - 107257 RMVar_ID_107257 Human_SNP_ID_415829662 m1A Human chr9 - 128167161 128167161 128167161 ATCCGAGGCCCACACTTGCATGTTTTCAGGTGAGGTCCAGAGATATATCCAGAGAGGAGTGGAAG ATCCGAGGCCCACACTTGCATGTTTTCAGGTGGGGTCCAGAGATATATCCAGAGAGGAGTGGAAG T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:128167076..128167227;chr9:128167076..128167175 26863196 MeRIP-seq:(Medium) rs1380460118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962260,Human_RBP_ID_3893998,Human_RBP_ID_3974822,Human_RBP_ID_9407454,Human_RBP_ID_9444455,Human_RBP_ID_18140644,Human_RBP_ID_19025666,Human_RBP_ID_19143949,Human_RBP_ID_21909147,Human_RBP_ID_21995966,Human_RBP_ID_22556741,Human_RBP_ID_22690280,Human_RBP_ID_23094835,Human_RBP_ID_23117261,Human_RBP_ID_26361128,Human_RBP_ID_26772668,Human_RBP_ID_26795925,Human_RBP_ID_27832731 Human_Splice_Rec_1084676,Human_Splice_Rec_1084677,Human_Splice_Rec_1084686,Human_Splice_Rec_1084687,Human_Splice_Rec_1084691,Human_Splice_Rec_1084722,Human_Splice_Rec_1084723,Human_Splice_Rec_1084754,Human_Splice_Rec_1084755,Human_Splice_Rec_1084786,Human_Splice_Rec_1084787,Human_Splice_Rec_1084820,Human_Splice_Rec_1084821,Human_Splice_Rec_1084854,Human_Splice_Rec_1084855,Human_Splice_Rec_1084860,Human_Splice_Rec_1084861,Human_Splice_Rec_1084890,Human_Splice_Rec_1084891,Human_Splice_Rec_1084922,Human_Splice_Rec_1084923,Human_Splice_Rec_1084956,Human_Splice_Rec_1084957,Human_Splice_Rec_1084994,Human_Splice_Rec_1084995,Human_Splice_Rec_1085022,Human_Splice_Rec_1085023,Human_Splice_Rec_1085038,Human_Splice_Rec_1085039,Human_Splice_Rec_1085046,Human_Splice_Rec_1085066,Human_Splice_Rec_1085067 RMVar_hsa_circ_25882,RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_297578 107258 RMVar_ID_107258 Human_SNP_ID_415829663 m1A Human chr9 - 128167161 128167161 128167161 ATCCGAGGCCCACACTTGCATGTTTTCAGGTGAGGTCCAGAGATATATCCAGAGAGGAGTGGAAG ATCCGAGGCCCACACTTGCATGTTTTCAGGTGCGGTCCAGAGATATATCCAGAGAGGAGTGGAAG T G CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:128167076..128167227;chr9:128167076..128167175 26863196 MeRIP-seq:(Medium) rs1380460118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962260,Human_RBP_ID_3893998,Human_RBP_ID_3974822,Human_RBP_ID_9407454,Human_RBP_ID_9444455,Human_RBP_ID_18140644,Human_RBP_ID_19025666,Human_RBP_ID_19143949,Human_RBP_ID_21909147,Human_RBP_ID_21995966,Human_RBP_ID_22556741,Human_RBP_ID_22690280,Human_RBP_ID_23094835,Human_RBP_ID_23117261,Human_RBP_ID_26361128,Human_RBP_ID_26772668,Human_RBP_ID_26795925,Human_RBP_ID_27832731 Human_Splice_Rec_1084676,Human_Splice_Rec_1084677,Human_Splice_Rec_1084686,Human_Splice_Rec_1084687,Human_Splice_Rec_1084691,Human_Splice_Rec_1084722,Human_Splice_Rec_1084723,Human_Splice_Rec_1084754,Human_Splice_Rec_1084755,Human_Splice_Rec_1084786,Human_Splice_Rec_1084787,Human_Splice_Rec_1084820,Human_Splice_Rec_1084821,Human_Splice_Rec_1084854,Human_Splice_Rec_1084855,Human_Splice_Rec_1084860,Human_Splice_Rec_1084861,Human_Splice_Rec_1084890,Human_Splice_Rec_1084891,Human_Splice_Rec_1084922,Human_Splice_Rec_1084923,Human_Splice_Rec_1084956,Human_Splice_Rec_1084957,Human_Splice_Rec_1084994,Human_Splice_Rec_1084995,Human_Splice_Rec_1085022,Human_Splice_Rec_1085023,Human_Splice_Rec_1085038,Human_Splice_Rec_1085039,Human_Splice_Rec_1085046,Human_Splice_Rec_1085066,Human_Splice_Rec_1085067 RMVar_hsa_circ_25882,RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_297578 107259 RMVar_ID_107259 Human_SNP_ID_415829711 m1A Human chr9 + 128167335 128167335 128167335 CTGAGCCTTTGCACATGGTGATCCTGCCTCCCAGAGTGCTCTTCCCAATCTATACTTTCTAGACT CTGAGCCTTTGCACATGGTGATCCTGCCTCCCGGAGTGCTCTTCCCAATCTATACTTTCTAGACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128167332..128167480 26863196 MeRIP-seq:(Medium) rs778189611 Functional Loss SNV dbSNP153 33..33 33 - - - 107260 RMVar_ID_107260 Human_SNP_ID_415830218 m1A Human chr9 + 128169366 128169366 128169366 AACTTGCTACACAGCCTTGGCCAAGGCTCTGTACCTCTCTGGGCCCATGTCCTCTGAGGGAGCTC AACTTGCTACACAGCCTTGGCCAAGGCTCTGTGCCTCTCTGGGCCCATGTCCTCTGAGGGAGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128169365..128169488 26863196 MeRIP-seq:(Medium) rs772696737 Functional Loss SNV dbSNP153 33..33 33 - - - 107261 RMVar_ID_107261 Human_SNP_ID_415832152 m1A Human chr9 - 128176363 128176363 128176363 GTCCCTGCTGCCCGTGCCCCGGGACGTCCTGGAGACAGAGGATGAGTGAGTGGGGGATCGTGGAA GTCCCTGCTGCCCGTGCCCCGGGACGTCCTGGGGACAGAGGATGAGTGAGTGGGGGATCGTGGAA T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128169451..128177775 32194978 MeRIP-seq:(Medium) rs771944672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712438,Human_RBP_ID_965070,Human_RBP_ID_3974824,Human_RBP_ID_8697206,Human_RBP_ID_17437216,Human_RBP_ID_18130178,Human_RBP_ID_18904053,Human_RBP_ID_19025669 Human_Splice_Rec_1084669,Human_Splice_Rec_1084715,Human_Splice_Rec_1084747,Human_Splice_Rec_1084779,Human_Splice_Rec_1084813,Human_Splice_Rec_1084845,Human_Splice_Rec_1084883,Human_Splice_Rec_1084915,Human_Splice_Rec_1084949,Human_Splice_Rec_1084987,Human_Splice_Rec_1085015,Human_Splice_Rec_1085029 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_73650 107262 RMVar_ID_107262 Human_SNP_ID_415832807 m1A Human chr9 - 128178852 128178852 128178852 AAGCGTCCAGCCACAGGAGCATCCTCCAGCGCAGGTGTCAGTACAGCCACCAGAGCAGACCCATG AAGCGTCCAGCCACAGGAGCATCCTCCAGCGCCGGTGTCAGTACAGCCACCAGAGCAGACCCATG T G CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128178805..128179065 26863196 MeRIP-seq:(Medium) rs1387411077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1119459,Human_RBP_ID_17323129,Human_RBP_ID_17437218,Human_RBP_ID_22629913 Human_Splice_Rec_1084662,Human_Splice_Rec_1084708,Human_Splice_Rec_1084772,Human_Splice_Rec_1084806,Human_Splice_Rec_1084908,Human_Splice_Rec_1084942,Human_Splice_Rec_1085078 RMVar_hsa_circ_32475,RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_81234,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_362446,RMVar_hsa_circ_259854,RMVar_hsa_circ_44120,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_259856 107263 RMVar_ID_107263 Human_SNP_ID_415833348 m1A Human chr9 - 128180513 128180513 128180513 CTCGCTCATGCCTCCATTCCAGACCAAGATTTACCGCCCTGCCCAGAGGACATCGCCAAGGAAAA CTCGCTCATGCCTCCATTCCAGACCAAGATTTGCCGCCCTGCCCAGAGGACATCGCCAAGGAAAA T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:128180386..128180561;chr9:128180426..128180525 26863196 MeRIP-seq:(Medium) rs1423677049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17323133,Human_RBP_ID_17437227,Human_RBP_ID_24549656,Human_RBP_ID_26361143 Human_Splice_Rec_1084658,Human_Splice_Rec_1084659,Human_Splice_Rec_1084704,Human_Splice_Rec_1084705,Human_Splice_Rec_1084738,Human_Splice_Rec_1084739,Human_Splice_Rec_1084768,Human_Splice_Rec_1084769,Human_Splice_Rec_1084802,Human_Splice_Rec_1084803,Human_Splice_Rec_1084836,Human_Splice_Rec_1084837,Human_Splice_Rec_1084874,Human_Splice_Rec_1084875,Human_Splice_Rec_1084904,Human_Splice_Rec_1084905,Human_Splice_Rec_1084938,Human_Splice_Rec_1084939,Human_Splice_Rec_1084978,Human_Splice_Rec_1084979,Human_Splice_Rec_1085006,Human_Splice_Rec_1085007,Human_Splice_Rec_1085056,Human_Splice_Rec_1085057,Human_Splice_Rec_1085074,Human_Splice_Rec_1085075,Human_Splice_Rec_1085088,Human_Splice_Rec_1085089,Human_Splice_Rec_1085098,Human_Splice_Rec_1085099,Human_Splice_Rec_1085110,Human_Splice_Rec_1085111,Human_Splice_Rec_1085118,Human_Splice_Rec_1085119,Human_Splice_Rec_1085132 Human_miRNA_ID_2424216,Human_miRNA_ID_2424217,Human_miRNA_ID_2424218,Human_miRNA_ID_2433878,Human_miRNA_ID_2433879,Human_miRNA_ID_2433880,Human_miRNA_ID_2570656,Human_miRNA_ID_2570657,Human_miRNA_ID_2570658 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_81234,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_259854,RMVar_hsa_circ_44120,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_53018,RMVar_hsa_circ_73909,RMVar_hsa_circ_259856 107264 RMVar_ID_107264 Human_SNP_ID_415833402 m1A Human chr9 + 128180684 128180684 128180684 CTGCTGACCCGCCCACTGGCCCCACCCCATTCATGTCCCTCTGAAGGGCCAGCAGCCTCCCTCCC CTGCTGACCCGCCCACTGGCCCCACCCCATTCTTGTCCCTCTGAAGGGCCAGCAGCCTCCCTCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128180682..128180825 26863196 MeRIP-seq:(Medium) rs746590919 Functional Loss SNV dbSNP153 33..33 33 - - - 107265 RMVar_ID_107265 Human_SNP_ID_415833460 m1A Human chr9 - 128180799 128180799 128180799 TTTCTGAAAGGAAGCAGGATTCTTCTTCTCAGACAATGCCTGTGGAAGACAAGTCAGACCCCCCA TTTCTGAAAGGAAGCAGGATTCTTCTTCTCAGGCAATGCCTGTGGAAGACAAGTCAGACCCCCCA T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128180751..128180825 26863196 MeRIP-seq:(Medium) rs954055234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91487,Human_RBP_ID_5010783,Human_RBP_ID_8925494,Human_RBP_ID_17437230,Human_RBP_ID_18904062 Human_Splice_Rec_1084656,Human_Splice_Rec_1084657,Human_Splice_Rec_1084702,Human_Splice_Rec_1084703,Human_Splice_Rec_1084736,Human_Splice_Rec_1084737,Human_Splice_Rec_1084766,Human_Splice_Rec_1084767,Human_Splice_Rec_1084800,Human_Splice_Rec_1084801,Human_Splice_Rec_1084834,Human_Splice_Rec_1084835,Human_Splice_Rec_1084872,Human_Splice_Rec_1084873,Human_Splice_Rec_1084902,Human_Splice_Rec_1084903,Human_Splice_Rec_1084936,Human_Splice_Rec_1084937,Human_Splice_Rec_1084976,Human_Splice_Rec_1084977,Human_Splice_Rec_1085004,Human_Splice_Rec_1085005,Human_Splice_Rec_1085054,Human_Splice_Rec_1085055,Human_Splice_Rec_1085073,Human_Splice_Rec_1085086,Human_Splice_Rec_1085087,Human_Splice_Rec_1085096,Human_Splice_Rec_1085097,Human_Splice_Rec_1085108,Human_Splice_Rec_1085109,Human_Splice_Rec_1085116,Human_Splice_Rec_1085117,Human_Splice_Rec_1085130,Human_Splice_Rec_1085131,Human_Splice_Rec_1085138 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_81234,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_259854,RMVar_hsa_circ_44120,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_53018,RMVar_hsa_circ_73909,RMVar_hsa_circ_259856 107266 RMVar_ID_107266 Human_SNP_ID_415834733 m1A Human chr9 + 128185682 128185682 128185682 GGTCCCAGCAAGGACTGGCGAGTGGCCTGGGGAAAGAACTGTTGCAAATTTGGAGTGGCCAGTTG GGTCCCAGCAAGGACTGGCGAGTGGCCTGGGGGAAGAACTGTTGCAAATTTGGAGTGGCCAGTTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128185631..128187868 32194978 MeRIP-seq:(Medium) rs1324098439 Functional Loss SNV dbSNP153 33..33 33 - - - 107267 RMVar_ID_107267 Human_SNP_ID_415835257 m1A Human chr9 + 128187922 128187922 128187922 CGGCAGTGTCATACGTGGCTGGTGGCATTGCAAACTGGTCCAGTCCTTTAGGAAAGCAATTCGGC CGGCAGTGTCATACGTGGCTGGTGGCATTGCAGACTGGTCCAGTCCTTTAGGAAAGCAATTCGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128187851..128187950 26863196 MeRIP-seq:(Medium) rs1249169064 Functional Loss SNV dbSNP153 33..33 33 - - - 107268 RMVar_ID_107268 Human_SNP_ID_415835965 m1A Human chr9 - 128190446 128190444 128190446 AAATAACCCTCTGACACCCCCTCCCAACACACAGGGGGCTCCCCCCGCAGCAGCCACAGCAGCCG AAATAACCCTCTGACACCCCCTCCCAACACAC__GGGGCTCCCCCCGCAGCAGCCACAGCAGCCG CCT C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128190410..128191298 32194978 MeRIP-seq:(Medium) rs1564300012 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9408576,Human_RBP_ID_22690288,Human_RBP_ID_22747795 RMVar_hsa_circ_98321,RMVar_hsa_circ_259853,RMVar_hsa_circ_121499,RMVar_hsa_circ_259856 107269 RMVar_ID_107269 Human_SNP_ID_415836293 m1A Human chr9 - 128191529 128191529 128191529 ACAGGCCCCGGAGTAGCAGCGGGGAGGCCGGGAGCCCGCGGGCCGGAGCCGCCCGGCCGAGGCGT ACAGGCCCCGGAGTAGCAGCGGGGAGGCCGGGGGCCCGCGGGCCGGAGCCGCCCGGCCGAGGCGT T C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128180385..128191740;chr9:128191409..128191575;chr9:128191068..128191575;chr9:128179140..128191740;chr9:128191367..128191575 26863196 MeRIP-seq:(Medium) rs1351003571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256105,Human_RBP_ID_5036443,Human_RBP_ID_9339079,Human_RBP_ID_17437237,Human_RBP_ID_18427224 Human_Splice_Rec_1084695,Human_Splice_Rec_1084727,Human_Splice_Rec_1084791,Human_Splice_Rec_1084865,Human_Splice_Rec_1085047,Human_Splice_Rec_1085083,Human_Splice_Rec_1085091 RMVar_hsa_circ_121499,RMVar_hsa_circ_259856 107270 RMVar_ID_107270 Human_SNP_ID_415836358 m1A Human chr9 - 128191698 128191698 128191698 TATGAGCCGCCCAGGACCCCCTCGCACCTGCTAGCGCCCCGCAGCCGCCCCCCAGCGTGACTTGT TATGAGCCGCCCAGGACCCCCTCGCACCTGCTGGCGCCCCGCAGCCGCCCCCCAGCGTGACTTGT T C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128191696..128191772 26863196 MeRIP-seq:(Medium) rs1392032158 Functional Loss SNV dbSNP153 33..33 33 - - - 107271 RMVar_ID_107271 Human_SNP_ID_415839333 m1A Human chr9 + 128203591 128203591 128203591 ACCTGCCGCAGATCGCTGTGGTGGGCGGCCAGAGCGCCGGCAAGAGCTCGGTGCTCGAGAATTTC ACCTGCCGCAGATCGCTGTGGTGGGCGGCCAGTGCGCCGGCAAGAGCTCGGTGCTCGAGAATTTC A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128203491..128203592 32194978 MeRIP-seq:(Medium) rs1564315125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1085157,Human_Splice_Rec_1085199,Human_Splice_Rec_1085239,Human_Splice_Rec_1085281,Human_Splice_Rec_1085323,Human_Splice_Rec_1085361,Human_Splice_Rec_1085379,Human_Splice_Rec_1085419,Human_Splice_Rec_1085459,Human_Splice_Rec_1085499 RMVar_hsa_circ_102982,RMVar_hsa_circ_259861 107272 RMVar_ID_107272 Human_SNP_ID_415844548 m1A Human chr9 - 128223006 128223006 128223006 GGTCCACCTCCCCAAGCTGGAGCCTGTCATGCAGGGAGCCAGAAAGTTGGGGTCGAGAGGACTGG GGTCCACCTCCCCAAGCTGGAGCCTGTCATGCGGGGAGCCAGAAAGTTGGGGTCGAGAGGACTGG T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128222977..128223077 32194978 MeRIP-seq:(Medium) rs962727328 Functional Loss SNV dbSNP153 33..33 33 - - - 107273 RMVar_ID_107273 Human_SNP_ID_415852574 m1A Human chr9 - 128254076 128254076 128254076 GCAGGCAGCCGGATGCCAGTGGCCATAGACTTATAAGTCTAAGAGGGGAGCCTCAGCTGGTCGGG GCAGGCAGCCGGATGCCAGTGGCCATAGACTTTTAAGTCTAAGAGGGGAGCCTCAGCTGGTCGGG T A RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128254050..128254201 32194978 MeRIP-seq:(Medium) rs1426897973 Functional Loss SNV dbSNP153 33..33 33 - - - 107274 RMVar_ID_107274 Human_SNP_ID_415852795 m1A Human chr9 + 128254719 128254719 128254719 GAGCCCCAGGCCCCCCTTCGACCTCTAAACAGATCCCTCCTCTTCTCGGAGACCTCCCTTTCCAA GAGCCCCAGGCCCCCCTTCGACCTCTAAACAGGTCCCTCCTCTTCTCGGAGACCTCCCTTTCCAA A G DNM1 Ensembl:ENSG00000106976 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128254670..128254755 26863196 MeRIP-seq:(Medium) rs760211178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712458,Human_RBP_ID_17094942 Human_Splice_Rec_1085238,Human_Splice_Rec_1085280,Human_Splice_Rec_1085322,Human_Splice_Rec_1085418,Human_Splice_Rec_1085458 107275 RMVar_ID_107275 Human_SNP_ID_415853102 m1A Human chr9 - 128255977 128255977 128255977 TACCTAGCAGAGGTTGGAGCTGGCACATGGGGAGGAGGTTCTAATAATTATTTGGGGCTGGGAAA TACCTAGCAGAGGTTGGAGCTGGCACATGGGGTGGAGGTTCTAATAATTATTTGGGGCTGGGAAA T A GOLGA2 Ensembl:ENSG00000167110 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128255929..128256046 26863196 MeRIP-seq:(Medium) rs1178402934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900493 RMVar_hsa_circ_93438,RMVar_hsa_circ_119177,RMVar_hsa_circ_128198,RMVar_hsa_circ_123417,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_259873,RMVar_hsa_circ_259875,RMVar_hsa_circ_88892,RMVar_hsa_circ_259874,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870 107276 RMVar_ID_107276 Human_SNP_ID_415853120 m1A Human chr9 - 128256066 128256066 128256066 GCTGCTGGGGTGGCCCTGCTTCCCCAGTGTACATATTGTATCTGTGTAACATTTTGTATATTCCA GCTGCTGGGGTGGCCCTGCTTCCCCAGTGTACGTATTGTATCTGTGTAACATTTTGTATATTCCA T C GOLGA2 Ensembl:ENSG00000167110 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128255927..128256127 32194978 MeRIP-seq:(Medium) rs577915688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712468,Human_RBP_ID_18173598,Human_RBP_ID_21906725 Human_miRNA_ID_757968 RMVar_hsa_circ_93438,RMVar_hsa_circ_119177,RMVar_hsa_circ_128198,RMVar_hsa_circ_123417,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_259873,RMVar_hsa_circ_259875,RMVar_hsa_circ_88892,RMVar_hsa_circ_259874,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870 107277 RMVar_ID_107277 Human_SNP_ID_415853121 m1A Human chr9 - 128256066 128256066 128256066 GCTGCTGGGGTGGCCCTGCTTCCCCAGTGTACATATTGTATCTGTGTAACATTTTGTATATTCCA GCTGCTGGGGTGGCCCTGCTTCCCCAGTGTACCTATTGTATCTGTGTAACATTTTGTATATTCCA T G GOLGA2 Ensembl:ENSG00000167110 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128255927..128256127 32194978 MeRIP-seq:(Medium) rs577915688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712468,Human_RBP_ID_18173598,Human_RBP_ID_21906725 Human_miRNA_ID_757968 RMVar_hsa_circ_93438,RMVar_hsa_circ_119177,RMVar_hsa_circ_128198,RMVar_hsa_circ_123417,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_259873,RMVar_hsa_circ_259875,RMVar_hsa_circ_88892,RMVar_hsa_circ_259874,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870 107278 RMVar_ID_107278 Human_SNP_ID_415853827 m1A Human chr9 - 128258158 128258156 128258159 TTTCAACTCAGCTGTAGCCAGTGCCGAGGAGGAGCAGGCAAGGCTACGTGGGCAGCTGAAGGAGC TTTCAACTCAGCTGTAGCCAGTGCCGAGGAG___CAGGCAAGGCTACGTGGGCAGCTGAAGGAGC GCTC G GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128257976..128258268 26863196 MeRIP-seq:(Medium) rs749587699 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_256265,Human_RBP_ID_965538,Human_RBP_ID_3974862,Human_RBP_ID_5124433,Human_RBP_ID_5154482,Human_RBP_ID_5408727,Human_RBP_ID_9408578,Human_RBP_ID_18140972,Human_RBP_ID_18173605,Human_RBP_ID_18414534,Human_RBP_ID_19024369,Human_RBP_ID_26361164,Human_RBP_ID_27832764 Human_Splice_Rec_1085694,Human_Splice_Rec_1085742,Human_Splice_Rec_1085754,Human_Splice_Rec_1085772 RMVar_hsa_circ_93438,RMVar_hsa_circ_119177,RMVar_hsa_circ_123417,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_259873,RMVar_hsa_circ_88892,RMVar_hsa_circ_259874,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_268691 107279 RMVar_ID_107279 Human_SNP_ID_415854425 m1A Human chr9 - 128260122 128260122 128260122 GTCGGAGCAGCACGTCAAGAGGGAGCTGGGAAAGAAGCTGGGCGAGCTGCAGGAGAAGCTGAGCG GTCGGAGCAGCACGTCAAGAGGGAGCTGGGAATGAAGCTGGGCGAGCTGCAGGAGAAGCTGAGCG T A GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128260076..128260200 26863196 MeRIP-seq:(Medium) rs975124711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847097,Human_RBP_ID_962264,Human_RBP_ID_3974866,Human_RBP_ID_8930650,Human_RBP_ID_9264681,Human_RBP_ID_9315208,Human_RBP_ID_9407463,Human_RBP_ID_19024373,Human_RBP_ID_26361172,Human_RBP_ID_27832772 Human_Splice_Rec_1085686,Human_Splice_Rec_1085687,Human_Splice_Rec_1085734,Human_Splice_Rec_1085735,Human_Splice_Rec_1085764,Human_Splice_Rec_1085765,Human_Splice_Rec_1085775,Human_Splice_Rec_1085784 Human_miRNA_ID_2012634,Human_miRNA_ID_2759010 RMVar_hsa_circ_93438,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_268691,RMVar_hsa_circ_259879 107280 RMVar_ID_107280 Human_SNP_ID_415854453 m1A Human chr9 - 128260186 128260186 128260186 GTGGCCGCTGATTGCTTCTCTCTGTCCAGACTAATGAGAACATGGAGATCACCAGCGCACTGCAG GTGGCCGCTGATTGCTTCTCTCTGTCCAGACTGATGAGAACATGGAGATCACCAGCGCACTGCAG T C GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128259043..128260209 32194978 MeRIP-seq:(Medium) rs1227009397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91755,Human_RBP_ID_9264682,Human_RBP_ID_9408582,Human_RBP_ID_16583124,Human_RBP_ID_22556239,Human_RBP_ID_22690310,Human_RBP_ID_22747801 Human_Splice_Rec_1085686,Human_Splice_Rec_1085734,Human_Splice_Rec_1085764,Human_Splice_Rec_1085784 RMVar_hsa_circ_93438,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_268691,RMVar_hsa_circ_259879 107281 RMVar_ID_107281 Human_SNP_ID_415854624 m1A Human chr9 - 128260619 128260619 128260619 CCGGGAGCAGGAGGAGAGGCTGCTGGAGCTGGAGCGGGCGGCCGAGCTCTGGGGGGAGCAGGCGG CCGGGAGCAGGAGGAGAGGCTGCTGGAGCTGGCGCGGGCGGCCGAGCTCTGGGGGGAGCAGGCGG T G GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:128260526..128260728 26863196 MeRIP-seq:(Medium) rs1293833943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797900,Human_RBP_ID_8930651,Human_RBP_ID_9315211,Human_RBP_ID_9408583,Human_RBP_ID_23094388,Human_RBP_ID_27843634 RMVar_hsa_circ_93438,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_268691,RMVar_hsa_circ_259879 107282 RMVar_ID_107282 Human_SNP_ID_415854667 m1A Human chr9 + 128260748 128260748 128260748 GCTCCTTCCGCAGGTGCTCAGCCTCCGCTTGTAGCTGCTGCTCCACCTCGGAGGGCCCTGCTGGG GCTCCTTCCGCAGGTGCTCAGCCTCCGCTTGTGGCTGCTGCTCCACCTCGGAGGGCCCTGCTGGG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128260438..128260994 26863196 MeRIP-seq:(Medium) rs759144089 Functional Loss SNV dbSNP153 33..33 33 - - - 107283 RMVar_ID_107283 Human_SNP_ID_415854805 m1A Human chr9 - 128261210 128261210 128261210 GGAGAAGGAATGTAGCATGAGTCGGGTACAGGAGCTGGAGACGAGCTTGGCTGAACTGAGGAACC GGAGAAGGAATGTAGCATGAGTCGGGTACAGGGGCTGGAGACGAGCTTGGCTGAACTGAGGAACC T C GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:128260438..128261750;chr9:128260455..128261575 26863196 MeRIP-seq:(Medium) rs768380441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965544,Human_RBP_ID_3975840,Human_RBP_ID_5124201,Human_RBP_ID_5482411,Human_RBP_ID_5633662,Human_RBP_ID_9264683,Human_RBP_ID_9315214,Human_RBP_ID_9407467,Human_RBP_ID_18414537,Human_RBP_ID_23094836,Human_RBP_ID_24549658,Human_RBP_ID_26361176,Human_RBP_ID_27832778 Human_Splice_Rec_1085682,Human_Splice_Rec_1085683,Human_Splice_Rec_1085730,Human_Splice_Rec_1085731,Human_Splice_Rec_1085790,Human_Splice_Rec_1085820,Human_Splice_Rec_1085832 Human_miRNA_ID_2717382 RMVar_hsa_circ_24354,RMVar_hsa_circ_93438,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_268691,RMVar_hsa_circ_55072,RMVar_hsa_circ_259879 107284 RMVar_ID_107284 Human_SNP_ID_415854810 m1A Human chr9 - 128261229 128261223 128261230 AGGTGCACACATTGAGAGAGGAGAAGGAATGTAGCATGAGTCGGGTACAGGAGCTGGAGACGAGC AGGTGCACACATTGAGAGAGGAGAAGGAATG_______AGTCGGGTACAGGAGCTGGAGACGAGC TCATGCTA T GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128261176..128261275 26863196 MeRIP-seq:(Medium) rs1467687863 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_91756,Human_RBP_ID_797903,Human_RBP_ID_3975840,Human_RBP_ID_5633663,Human_RBP_ID_9264683,Human_RBP_ID_9315214,Human_RBP_ID_18414537,Human_RBP_ID_23094836,Human_RBP_ID_24549658,Human_RBP_ID_26361176,Human_RBP_ID_27832778 Human_Splice_Rec_1085682,Human_Splice_Rec_1085683,Human_Splice_Rec_1085730,Human_Splice_Rec_1085731,Human_Splice_Rec_1085790,Human_Splice_Rec_1085820,Human_Splice_Rec_1085832 Human_miRNA_ID_2243282,Human_miRNA_ID_2244299,Human_miRNA_ID_2717382 RMVar_hsa_circ_24354,RMVar_hsa_circ_93438,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_268691,RMVar_hsa_circ_55072,RMVar_hsa_circ_259879 107285 RMVar_ID_107285 Human_SNP_ID_415854880 m1A Human chr9 - 128261470 128261470 128261470 AGGAGAGAGCGCCATGTGGCGGCAGAGGATGCAGCAGATGTCAGAGCAGGTGAGACCTGACCCTT AGGAGAGAGCGCCATGTGGCGGCAGAGGATGCGGCAGATGTCAGAGCAGGTGAGACCTGACCCTT T C GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:128261451..128261575 26863196 MeRIP-seq:(Medium) rs766238964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15819,Human_RBP_ID_797904,Human_RBP_ID_847101,Human_RBP_ID_965545,Human_RBP_ID_3974869,Human_RBP_ID_5633664,Human_RBP_ID_9264684,Human_RBP_ID_9407468,Human_RBP_ID_18414538,Human_RBP_ID_23094391,Human_RBP_ID_26361178,Human_RBP_ID_27833488 Human_Splice_Rec_1085680,Human_Splice_Rec_1085681,Human_Splice_Rec_1085728,Human_Splice_Rec_1085729,Human_Splice_Rec_1085788,Human_Splice_Rec_1085789,Human_Splice_Rec_1085818,Human_Splice_Rec_1085819,Human_Splice_Rec_1085830,Human_Splice_Rec_1085831 Human_miRNA_ID_2721944,Human_miRNA_ID_2907425,Human_miRNA_ID_3026261 RMVar_hsa_circ_24354,RMVar_hsa_circ_93438,RMVar_hsa_circ_259871,RMVar_hsa_circ_88892,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_55072,RMVar_hsa_circ_259879,RMVar_hsa_circ_88631,RMVar_hsa_circ_358750,RMVar_hsa_circ_361666,RMVar_hsa_circ_259880 107286 RMVar_ID_107286 Human_SNP_ID_415855256 m1A Human chr9 + 128262947 128262944 128262947 TGGGCACACATGCACACCTCTATGACTACCTCATCATGCTTACCTGTACCCCCCACCTCCCAGCA TGGGCACACATGCACACCTCTATGACTACC___TCATGCTTACCTGTACCCCCCACCTCCCAGCA CTCA C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128262933..128263037 26863196 MeRIP-seq:(Medium) rs1366578009 Functional Loss DEL dbSNP153 31..33 33 - - - 107287 RMVar_ID_107287 Human_SNP_ID_415858848 m1A Human chr9 - 128276326 128276326 128276326 TGGCGCAAGAGGGTCCAGCGCGGGAGTCGGAGAGCGACCTCTCAGGTGCACCGGGCCAGGAACTC TGGCGCAAGAGGGTCCAGCGCGGGAGTCGGAGGGCGACCTCTCAGGTGCACCGGGCCAGGAACTC T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128276276..128276688 26863196 MeRIP-seq:(Medium) rs971289652 Functional Loss SNV dbSNP153 33..33 33 - - - 107288 RMVar_ID_107288 Human_SNP_ID_415858877 m1A Human chr9 - 128276372 128276372 128276372 ACCTCCTGAGCCCTGGGGTCCGAGGCCCCCGGATCAGGGGGTTCAATGGCGCAAGAGGGTCCAGC ACCTCCTGAGCCCTGGGGTCCGAGGCCCCCGGCTCAGGGGGTTCAATGGCGCAAGAGGGTCCAGC T G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128276327..128276711 32194978 MeRIP-seq:(Medium) rs1221253001 Functional Loss SNV dbSNP153 33..33 33 - - - 107289 RMVar_ID_107289 Human_SNP_ID_415858954 m1A Human chr9 - 128276613 128276613 128276613 CTGTGGGGATGCGGGAGGAGGAGCAGTTGGGAAGTAGGAGCGCCAGGGACTGGATCCATCTGGAA CTGTGGGGATGCGGGAGGAGGAGCAGTTGGGAGGTAGGAGCGCCAGGGACTGGATCCATCTGGAA T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:128276327..128276612 26863410 MeRIP-seq:(Medium) rs762789885 Functional Loss SNV dbSNP153 33..33 33 - - - 107290 RMVar_ID_107290 Human_SNP_ID_415859012 m1A Human chr9 + 128276749 128276749 128276749 AGACTTACCCGAAGTTGCCGCGGGGCCTTCCGATCCCCTGTGAGTATTTCTTCCCCCACACCCCC AGACTTACCCGAAGTTGCCGCGGGGCCTTCCGCTCCCCTGTGAGTATTTCTTCCCCCACACCCCC A C SWI5 Ensembl:ENSG00000175854 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128276726..128276750 32194978 MeRIP-seq:(Medium) rs1346244445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036447 Human_Splice_Rec_1085860,Human_Splice_Rec_1085861,Human_Splice_Rec_1085868,Human_Splice_Rec_1085869,Human_Splice_Rec_1085879,Human_Splice_Rec_1085887,Human_Splice_Rec_1085894,Human_Splice_Rec_1085895,Human_Splice_Rec_1085907,Human_Splice_Rec_1085912,Human_Splice_Rec_1085913 RMVar_hsa_circ_77572,RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_259892,RMVar_hsa_circ_259893 107291 RMVar_ID_107291 Human_SNP_ID_415861071 m1A Human chr9 + 128284570 128284570 128284570 ATGGGACCAGCGAGGAGTCTCTGCACCTTGACATTCAGAAACTGAAGGAGAAGAGGGACATGCTG ATGGGACCAGCGAGGAGTCTCTGCACCTTGACTTTCAGAAACTGAAGGAGAAGAGGGACATGCTG A T SWI5 Ensembl:ENSG00000175854 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128284516..128286074 32194978 MeRIP-seq:(Medium) rs759510514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712487,Human_RBP_ID_5037496,Human_RBP_ID_5633668,Human_RBP_ID_8697264,Human_RBP_ID_17437246,Human_RBP_ID_23094495,Human_RBP_ID_27833499 Human_Splice_Rec_1085862,Human_Splice_Rec_1085863,Human_Splice_Rec_1085872,Human_Splice_Rec_1085873,Human_Splice_Rec_1085880,Human_Splice_Rec_1085881,Human_Splice_Rec_1085888,Human_Splice_Rec_1085889,Human_Splice_Rec_1085896,Human_Splice_Rec_1085897,Human_Splice_Rec_1085908,Human_Splice_Rec_1085909,Human_Splice_Rec_1085914,Human_Splice_Rec_1085915 RMVar_hsa_circ_77572,RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_126252,RMVar_hsa_circ_259892,RMVar_hsa_circ_259893,RMVar_hsa_circ_325787,RMVar_hsa_circ_259894 107292 RMVar_ID_107292 Human_SNP_ID_415862162 m1A Human chr9 + 128288739 128288739 128288739 GAATGACTGAGCAGGCTCATCGCCCCTTGTCCACAGCTCCCAGGGACAGAAGGGTGTGGACATGA GAATGACTGAGCAGGCTCATCGCCCCTTGTCCGCAGCTCCCAGGGACAGAAGGGTGTGGACATGA A G SWI5 Ensembl:ENSG00000175854 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128288689..128288790 32194978 MeRIP-seq:(Medium) rs181209395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712488,Human_RBP_ID_17666582,Human_RBP_ID_24287591 Human_Splice_Rec_1085866,Human_Splice_Rec_1085876,Human_Splice_Rec_1085884,Human_Splice_Rec_1085892,Human_Splice_Rec_1085918 RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_92526,RMVar_hsa_circ_126252,RMVar_hsa_circ_259893,RMVar_hsa_circ_83200,RMVar_hsa_circ_259894,RMVar_hsa_circ_259895,RMVar_hsa_circ_259896 107293 RMVar_ID_107293 Human_SNP_ID_415862163 m1A Human chr9 + 128288739 128288739 128288739 GAATGACTGAGCAGGCTCATCGCCCCTTGTCCACAGCTCCCAGGGACAGAAGGGTGTGGACATGA GAATGACTGAGCAGGCTCATCGCCCCTTGTCCTCAGCTCCCAGGGACAGAAGGGTGTGGACATGA A T SWI5 Ensembl:ENSG00000175854 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128288689..128288790 32194978 MeRIP-seq:(Medium) rs181209395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712488,Human_RBP_ID_17666582,Human_RBP_ID_24287591 Human_Splice_Rec_1085866,Human_Splice_Rec_1085876,Human_Splice_Rec_1085884,Human_Splice_Rec_1085892,Human_Splice_Rec_1085918 RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_92526,RMVar_hsa_circ_126252,RMVar_hsa_circ_259893,RMVar_hsa_circ_83200,RMVar_hsa_circ_259894,RMVar_hsa_circ_259895,RMVar_hsa_circ_259896 107294 RMVar_ID_107294 Human_SNP_ID_415867615 m1A Human chr9 - 128309374 128309374 128309374 ACTTGACCCAACTGAGAAGGAAAAACTTCTGTATGGAGGAAAAGACAGTAAACATGACAGACTGA ACTTGACCCAACTGAGAAGGAAAAACTTCTGTGTGGAGGAAAAGACAGTAAACATGACAGACTGA T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128309325..128309416 26863196 MeRIP-seq:(Medium) rs1478530476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712497,Human_RBP_ID_2061077,Human_RBP_ID_7900541,Human_RBP_ID_8697280,Human_RBP_ID_17323366,Human_RBP_ID_18904106,Human_RBP_ID_24287599 Human_miRNA_ID_267142 107295 RMVar_ID_107295 Human_SNP_ID_415870943 m1A Human chr9 - 128321578 128321578 128321578 ACCATCCACTGGGTAAGGCAGATTTAAGCAGGATCCTGTGTGTCACTTCCCAGGAAATCCCTGAG ACCATCCACTGGGTAAGGCAGATTTAAGCAGGTTCCTGTGTGTCACTTCCCAGGAAATCCCTGAG T A TRUB2 Ensembl:ENSG00000167112 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128321576..128321625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5410072 RMVar_hsa_circ_115075,RMVar_hsa_circ_75593,RMVar_hsa_circ_88703,RMVar_hsa_circ_259897,RMVar_hsa_circ_259898,RMVar_hsa_circ_270130,RMVar_hsa_circ_259899,RMVar_hsa_circ_259900 107296 RMVar_ID_107296 Human_SNP_ID_415870944 m1A Human chr9 - 128321578 128321578 128321578 ACCATCCACTGGGTAAGGCAGATTTAAGCAGGATCCTGTGTGTCACTTCCCAGGAAATCCCTGAG ACCATCCACTGGGTAAGGCAGATTTAAGCAGGCTCCTGTGTGTCACTTCCCAGGAAATCCCTGAG T G TRUB2 Ensembl:ENSG00000167112 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128321576..128321625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5410072 RMVar_hsa_circ_115075,RMVar_hsa_circ_75593,RMVar_hsa_circ_88703,RMVar_hsa_circ_259897,RMVar_hsa_circ_259898,RMVar_hsa_circ_270130,RMVar_hsa_circ_259899,RMVar_hsa_circ_259900 107297 RMVar_ID_107297 Human_SNP_ID_415871288 m1A Human chr9 + 128322390 128322390 128322390 CTTATAGACCGCGAAAAGCCCATGCAGCCGCGACAAGCCAGCAGACCCCATACTTGAAGATCACA CTTATAGACCGCGAAAAGCCCATGCAGCCGCGGCAAGCCAGCAGACCCCATACTTGAAGATCACA A G NONHSAG053531.2-001 RNACentral:URS00009B4E16 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128322299..128322400 26863196 MeRIP-seq:(Medium) rs771308348 Functional Loss SNV dbSNP153 33..33 33 - - - 107298 RMVar_ID_107298 Human_SNP_ID_415871498 m1A Human chr9 - 128322872 128322872 128322872 GGAGCCCGCAGAGCCGACGGAGGACAGGGCGCAGCAGAGTCGCCATGGCAGCGGGCGTCCGCGGA GGAGCCCGCAGAGCCGACGGAGGACAGGGCGCTGCAGAGTCGCCATGGCAGCGGGCGTCCGCGGA T A RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128322826..128323150 26863196 MeRIP-seq:(Medium) rs1348290022 Functional Loss SNV dbSNP153 33..33 33 - - - 107299 RMVar_ID_107299 Human_SNP_ID_415871499 m1A Human chr9 - 128322872 128322872 128322872 GGAGCCCGCAGAGCCGACGGAGGACAGGGCGCAGCAGAGTCGCCATGGCAGCGGGCGTCCGCGGA GGAGCCCGCAGAGCCGACGGAGGACAGGGCGCCGCAGAGTCGCCATGGCAGCGGGCGTCCGCGGA T G RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128322826..128323150 26863196 MeRIP-seq:(Medium) rs1348290022 Functional Loss SNV dbSNP153 33..33 33 - - - 107300 RMVar_ID_107300 Human_SNP_ID_415871523 m1A Human chr9 - 128322893 128322893 128322893 CCGCAGGCCGCTGTAGGCCCGGGAGCCCGCAGAGCCGACGGAGGACAGGGCGCAGCAGAGTCGCC CCGCAGGCCGCTGTAGGCCCGGGAGCCCGCAGGGCCGACGGAGGACAGGGCGCAGCAGAGTCGCC T C RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128322542..128323199 26863196 MeRIP-seq:(Medium) rs1185105843 Functional Loss SNV dbSNP153 33..33 33 - - - 107301 RMVar_ID_107301 Human_SNP_ID_415871545 m1A Human chr9 + 128322927 128322927 128322927 TGCGGGCTCCCGGGCCTACAGCGGCCTGCGGCAGGCAAGTGGCGCCGGGTTCTGGGCGCAGGCGG TGCGGGCTCCCGGGCCTACAGCGGCCTGCGGCGGGCAAGTGGCGCCGGGTTCTGGGCGCAGGCGG A G COQ4 Ensembl:ENSG00000167113 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128322826..128323150 26863410 MeRIP-seq:(Medium) rs1170981278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036452,Human_RBP_ID_19145932 RMVar_hsa_circ_124412,RMVar_hsa_circ_259901 107302 RMVar_ID_107302 Human_SNP_ID_415871623 m1A Human chr9 + 128323067 128323067 128323067 GAGCGACGGCGCCGGCCCGCTATACTCGCACCACCTCCCCACCTCCCCGCTGCAGAAAGGGCTGT GAGCGACGGCGCCGGCCCGCTATACTCGCACCGCCTCCCCACCTCCCCGCTGCAGAAAGGGCTGT A G COQ4 Ensembl:ENSG00000167113 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:128322801..128323290 26863196 MeRIP-seq:(Medium) rs748282472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5124204,Human_RBP_ID_8697293,Human_RBP_ID_23094497,Human_RBP_ID_24287604 Human_Splice_Rec_1085951,Human_Splice_Rec_1085953,Human_Splice_Rec_1085963 Human_miRNA_ID_2367005,Human_miRNA_ID_2725614,Human_miRNA_ID_3014807 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_78090,RMVar_hsa_circ_99555,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259904,RMVar_hsa_circ_259905,RMVar_hsa_circ_259903 107303 RMVar_ID_107303 Human_SNP_ID_415871672 m1A Human chr9 + 128323139 128323139 128323139 CGGCTCCGCGGCGATGGCGCTCTATAACCCCTACCGCCACGGTAAGGCCGCCCGCGCCTCGCCCC CGGCTCCGCGGCGATGGCGCTCTATAACCCCTGCCGCCACGGTAAGGCCGCCCGCGCCTCGCCCC A G COQ4 Ensembl:ENSG00000167113 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128322901..128323385 26863196 MeRIP-seq:(Medium) rs1392581380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5430962,Human_RBP_ID_19143976,Human_RBP_ID_23094497,Human_RBP_ID_27370650,Human_RBP_ID_27570306 Human_Splice_Rec_1085951,Human_Splice_Rec_1085953,Human_Splice_Rec_1085963 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_78090,RMVar_hsa_circ_99555,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259904,RMVar_hsa_circ_259905,RMVar_hsa_circ_259903 107304 RMVar_ID_107304 Human_SNP_ID_415874545 m1A Human chr9 - 128333687 128333687 128333687 AGTCAAGGGAGCCCTCTGCCTCCAAGGGAAGCAGGGGATGGGGGAGGTAGGCCAGGCCCCGCTGG AGTCAAGGGAGCCCTCTGCCTCCAAGGGAAGCGGGGGATGGGGGAGGTAGGCCAGGCCCCGCTGG T C RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128333476..128333725 32194978 MeRIP-seq:(Medium) rs779617452 Functional Loss SNV dbSNP153 33..33 33 - - - 107305 RMVar_ID_107305 Human_SNP_ID_415876491 m1A Human chr9 - 128340780 128340780 128340780 CCCGTCCAGATGCGGCCCGGTTGCAGCAGCGTAGACAGCGTGAGGGGCATTAGCCGCCCCTGGAC CCCGTCCAGATGCGGCCCGGTTGCAGCAGCGTTGACAGCGTGAGGGGCATTAGCCGCCCCTGGAC T A RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128340513..128340894 26863196 MeRIP-seq:(Medium) rs1289669475 Functional Loss SNV dbSNP153 33..33 33 - - - 107306 RMVar_ID_107306 Human_SNP_ID_415876501 m1A Human chr9 + 128340802 128340802 128340802 TCACGCTGTCTACGCTGCTGCAACCGGGCCGCATCTGGACGGGGCGCCGCGCGGCGGAGCCGACG TCACGCTGTCTACGCTGCTGCAACCGGGCCGCCTCTGGACGGGGCGCCGCGCGGCGGAGCCGACG A C SLC27A4 Ensembl:ENSG00000167114 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128340698..128343131 26863196 MeRIP-seq:(Medium) rs1330608328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5011071,Human_RBP_ID_9442035,Human_RBP_ID_18130227 Human_Splice_Rec_1085969,Human_Splice_Rec_1085993 107307 RMVar_ID_107307 Human_SNP_ID_415877230 m1A Human chr9 + 128343176 128343176 128343176 AGCCTCTCTGGTGGGGGTGCTGCTGTTCTCCAAGCTGGTGCTGAAACTGCCCTGGACCCAGGTGG AGCCTCTCTGGTGGGGGTGCTGCTGTTCTCCAGGCTGGTGCTGAAACTGCCCTGGACCCAGGTGG A G SLC27A4 Ensembl:ENSG00000167114 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128343072..128343228 26863196 MeRIP-seq:(Medium) rs774441905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1702335,Human_RBP_ID_2061092,Human_RBP_ID_5035895,Human_RBP_ID_19024377 Human_Splice_Rec_1085970,Human_Splice_Rec_1085994 RMVar_hsa_circ_2224,RMVar_hsa_circ_46482 107308 RMVar_ID_107308 Human_SNP_ID_415880805 m1A Human chr9 - 128355189 128355188 128355190 AGGAAGGGGCTGTGAAGGGCTGGGGACCCACCAGTAAGGTAGGCCTGGTCCCCCTTCTTGAAGAC AGGAAGGGGCTGTGAAGGGCTGGGGACCCAC__GTAAGGTAGGCCTGGTCCCCCTTCTTGAAGAC CTG C RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:128355148..128355220;chr9:128355118..128355223 26863196 MeRIP-seq:(Medium) rs763625583 Functional Loss DEL dbSNP153 32..33 33 - - - 107309 RMVar_ID_107309 Human_SNP_ID_415881038 m1A Human chr9 - 128355750 128355750 128355750 TCAGGCAGGAGGCGCAGGAAGATGGGGCGCGCATACAGGGGCAGTTCCTTCTCCAAGACCTGAGC TCAGGCAGGAGGCGCAGGAAGATGGGGCGCGCGTACAGGGGCAGTTCCTTCTCCAAGACCTGAGC T C RF00017-1784,RF00017-4503,RF00017-4501 RNACentral:URS0000904F64,RNACentral:URS0000948B80,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128355617..128355750 26863196 MeRIP-seq:(Medium) rs1481584886 Functional Loss SNV dbSNP153 33..33 33 - - - 107310 RMVar_ID_107310 Human_SNP_ID_415882371 m1A Human chr9 + 128360791 128360791 128360791 ATGATGTCTTGGGTGAGGGTAGGGAGAGGACAAGGGGTCACCGAGCCCTTCCCAGAGAGCAGGGA ATGATGTCTTGGGTGAGGGTAGGGAGAGGACAGGGGGTCACCGAGCCCTTCCCAGAGAGCAGGGA A G SLC27A4 Ensembl:ENSG00000167114 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128360744..128360947 26863196 MeRIP-seq:(Medium) rs988806703 Functional Loss SNV dbSNP153 33..33 33 - - - 107311 RMVar_ID_107311 Human_SNP_ID_415887166 m1A Human chr9 + 128379024 128379024 128379024 GGGTAACTGTCAGGATAGCCTAGGGGCTGGGGACCGGATATGGCAGGTGTTCACTGTAACCTTAG GGGTAACTGTCAGGATAGCCTAGGGGCTGGGGGCCGGATATGGCAGGTGTTCACTGTAACCTTAG A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128379020..128379179 26863196 MeRIP-seq:(Medium) rs1419760987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900625,Human_RBP_ID_16584287 RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 107312 RMVar_ID_107312 Human_SNP_ID_415889285 m1A Human chr9 + 128387864 128387864 128387864 GCTCATCTGGATCAAGAAGAATTTGCTAAAAGAGCGGCCAGAGTTGTTCATCCAGGGAGACAGCG GCTCATCTGGATCAAGAAGAATTTGCTAAAAGCGCGGCCAGAGTTGTTCATCCAGGGAGACAGCG A C URM1 Ensembl:ENSG00000167118 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128387770..128387926 26863196 MeRIP-seq:(Medium) rs1245654675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_965088,Human_RBP_ID_3975854,Human_RBP_ID_9407481,Human_RBP_ID_19024380,Human_RBP_ID_26361186,Human_RBP_ID_26833602 Human_Splice_Rec_1086004,Human_Splice_Rec_1086005,Human_Splice_Rec_1086012,Human_Splice_Rec_1086016,Human_Splice_Rec_1086020,Human_Splice_Rec_1086021,Human_Splice_Rec_1086028,Human_Splice_Rec_1086029 Human_miRNA_ID_2783934 RMVar_hsa_circ_115758,RMVar_hsa_circ_259916,RMVar_hsa_circ_102816,RMVar_hsa_circ_259915,RMVar_hsa_circ_370717,RMVar_hsa_circ_259917 107313 RMVar_ID_107313 Human_SNP_ID_415889858 m1A Human chr9 + 128389786 128389786 128389786 GGCACCCTTAGAGGGGAGAACGAAGCAATCAGACATCCCCTTGGGCCCTGCTTCCAGGTCTCCCT GGCACCCTTAGAGGGGAGAACGAAGCAATCAGCCATCCCCTTGGGCCCTGCTTCCAGGTCTCCCT A C URM1 Ensembl:ENSG00000167118 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128389736..128390134 32194978 MeRIP-seq:(Medium) rs1189313018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712572,Human_RBP_ID_5011160 Human_miRNA_ID_2573232,Human_miRNA_ID_2979152 RMVar_hsa_circ_115758,RMVar_hsa_circ_102816,RMVar_hsa_circ_259915,RMVar_hsa_circ_259917,RMVar_hsa_circ_126130,RMVar_hsa_circ_259918 107314 RMVar_ID_107314 Human_SNP_ID_415889863 m1A Human chr9 - 128389802 128389802 128389802 GGCAGGCAAGGGGGACAGGGAGACCTGGAAGCAGGGCCCAAGGGGATGTCTGATTGCTTCGTTCT GGCAGGCAAGGGGGACAGGGAGACCTGGAAGCCGGGCCCAAGGGGATGTCTGATTGCTTCGTTCT T G RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:128389751..128390538;chr9:128389751..128389975 26863196 MeRIP-seq:(Medium) rs1266868590 Functional Loss SNV dbSNP153 33..33 33 - - - 107315 RMVar_ID_107315 Human_SNP_ID_415889978 m1A Human chr9 - 128390283 128390283 128390283 TGGCTGGAGGAGCAGCTGCTGGCGGTGGGGGGAGTCGGCACTCAATAGGGGACCCCAGCTGGGGT TGGCTGGAGGAGCAGCTGCTGGCGGTGGGGGGGGTCGGCACTCAATAGGGGACCCCAGCTGGGGT T C RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128390226..128390450 26863196 MeRIP-seq:(Medium) rs1046557713 Functional Loss SNV dbSNP153 33..33 33 - - - 107316 RMVar_ID_107316 Human_SNP_ID_415897954 m1A Human chr9 - 128420886 128420870 128420886 AGCAGCAGCTGGAGCAGCGGCGCGGCGCGGGCAGCGCGCATGGCGGGCGCTTGGGCGGCTGCAGC AGCAGCAGCTGGAGCAGCGGCGCGGCGCGGGC________________GCTTGGGCGGCTGCAGC CGCCCGCCATGCGCGCT C RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128420851..128421295 26863196 MeRIP-seq:(Medium) rs760654749 Functional Loss DEL dbSNP153 33..48 33 - - - 107317 RMVar_ID_107317 Human_SNP_ID_415897998 m1A Human chr9 - 128420951 128420951 128420951 CAAGGACCACGGCGGGCAGCGGCGACTCCGCAACGCCCGCAGCCTCCAGCCACGGCCCCAGCAGG CAAGGACCACGGCGGGCAGCGGCGACTCCGCAGCGCCCGCAGCCTCCAGCCACGGCCCCAGCAGG T C RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128420851..128421025 26863410 MeRIP-seq:(Medium) rs1242177599 Functional Loss SNV dbSNP153 33..33 33 - - - 107318 RMVar_ID_107318 Human_SNP_ID_415898541 m1A Human chr9 - 128422964 128422964 128422964 TTCCCCTCAGATCACCACCTGGGCTCGCCCTCAGGCCTCCAGACCACAGCAGCATAGTCATCGCC TTCCCCTCAGATCACCACCTGGGCTCGCCCTCTGGCCTCCAGACCACAGCAGCATAGTCATCGCC T A RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128422914..128423010 26863196 MeRIP-seq:(Medium) rs1433716277 Functional Loss SNV dbSNP153 33..33 33 - - - 107319 RMVar_ID_107319 Human_SNP_ID_415898547 m1A Human chr9 + 128422977 128422977 128422977 CTGCTGTGGTCTGGAGGCCTGAGGGCGAGCCCAGGTGGTGATCTGAGGGGAAGGGTGCTGGGGAA CTGCTGTGGTCTGGAGGCCTGAGGGCGAGCCCGGGTGGTGATCTGAGGGGAAGGGTGCTGGGGAA A G CERCAM Ensembl:ENSG00000167123 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128422929..128423079 32194978 MeRIP-seq:(Medium) rs1356061966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962271,Human_RBP_ID_3974879 Human_Splice_Rec_1086033,Human_Splice_Rec_1086039,Human_Splice_Rec_1086063,Human_Splice_Rec_1086069,Human_Splice_Rec_1086083,Human_Splice_Rec_1086089,Human_Splice_Rec_1086111 RMVar_hsa_circ_7288,RMVar_hsa_circ_83657,RMVar_hsa_circ_305178,RMVar_hsa_circ_259919,RMVar_hsa_circ_343758,RMVar_hsa_circ_16358,RMVar_hsa_circ_259920 107320 RMVar_ID_107320 Human_SNP_ID_415901773 m1A Human chr9 - 128434118 128434118 128434118 GCACGTCATCCTCAAACACCAGGACCCGGGCCAGGCCCCTGGCAACCACCTGTGGCATACAATGG GCACGTCATCCTCAAACACCAGGACCCGGGCCGGGCCCCTGGCAACCACCTGTGGCATACAATGG T C RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128434101..128434125 26863196 MeRIP-seq:(Medium) rs1283980118 Functional Loss SNV dbSNP153 33..33 33 - - - 107321 RMVar_ID_107321 Human_SNP_ID_415902709 m1A Human chr9 + 128437297 128437297 128437297 GTACAGGGAGGTAAAGCAGGACCCTTGCAGACATGTTGCCCAGCACACAGTAGGCCCTCAATAAA GTACAGGGAGGTAAAGCAGGACCCTTGCAGACCTGTTGCCCAGCACACAGTAGGCCCTCAATAAA A C CERCAM Ensembl:ENSG00000167123 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_185202,Human_RBP_ID_17323487,Human_RBP_ID_18963114 GWAS_ID_14730,GWAS_ID_14731,GWAS_ID_14732,GWAS_ID_14733,GWAS_ID_14734,GWAS_ID_14735,GWAS_ID_14736,GWAS_ID_14737 107322 RMVar_ID_107322 Human_SNP_ID_415908168 m1A Human chr9 - 128456254 128456254 128456254 CGCTGGATCCCGCCTGCCGGCGGCCTCTCACCAGGAGCGACACGGCTGCGCCCAGAAACGCCGCC CGCTGGATCCCGCCTGCCGGCGGCCTCTCACCCGGAGCGACACGGCTGCGCCCAGAAACGCCGCC T G lnc-TRUB2-2,RF00017-4503,lnc-TRUB2-2:2 RNACentral:URS00009B33D0,RNACentral:URS0000948B80,RNACentral:URS00009C2333 lincRNA,SRP RNA,lincRNA intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:128456218..128456370 26863196 MeRIP-seq:(Medium) rs1298522263 Functional Loss SNV dbSNP153 33..33 33 - - - 107323 RMVar_ID_107323 Human_SNP_ID_415908554 m1A Human chr9 - 128457203 128457203 128457203 AGGCGCTCCTCTACTGTCCAAGTCGCACAGCAACTGTCCTGCCAAAGTAGGGGGAAATAGTAGAG AGGCGCTCCTCTACTGTCCAAGTCGCACAGCAGCTGTCCTGCCAAAGTAGGGGGAAATAGTAGAG T C RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128457196..128457366 26863196 MeRIP-seq:(Medium) rs1293588264 Functional Loss SNV dbSNP153 33..33 33 - - - 107324 RMVar_ID_107324 Human_SNP_ID_415909291 m1A Human chr9 - 128459651 128459650 128459652 GGCTGCTACGTGAGTGCATCACCTACCGTCACAGTTACACTGGGTGCGCCACAAGGTGCTCTCAA GGCTGCTACGTGAGTGCATCACCTACCGTCA__GTTACACTGGGTGCGCCACAAGGTGCTCTCAA CTG C RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128459601..128459675 32194978 MeRIP-seq:(Medium) rs779884499 Functional Loss DEL dbSNP153 32..33 33 - - - 107325 RMVar_ID_107325 Human_SNP_ID_415909567 m1A Human chr9 - 128460615 128460613 128460615 GGTTTCGGGAGTTTTTTTATGTGGACGTGGACAGGGGTGTTCTCATCCACGTGAACATGTAAGGG GGTTTCGGGAGTTTTTTTATGTGGACGTGGAC__GGGTGTTCTCATCCACGTGAACATGTAAGGG CCT C RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128460564..128460663 26863196 MeRIP-seq:(Medium) rs755396237 Functional Loss DEL dbSNP153 33..34 33 - - - 107326 RMVar_ID_107326 Human_SNP_ID_415909569 m1A Human chr9 - 128460615 128460615 128460615 GGTTTCGGGAGTTTTTTTATGTGGACGTGGACAGGGGTGTTCTCATCCACGTGAACATGTAAGGG GGTTTCGGGAGTTTTTTTATGTGGACGTGGACCGGGGTGTTCTCATCCACGTGAACATGTAAGGG T G RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128460564..128460663 26863196 MeRIP-seq:(Medium) rs1184855664 Functional Loss SNV dbSNP153 33..33 33 - - - 107327 RMVar_ID_107327 Human_SNP_ID_415912666 m1A Human chr9 + 128471411 128471411 128471411 GGTGGCCCACGAACTGGCTGAGACTGAGCACGAGAACACGGTGTTGAGGCACAACATCGAGCGCA GGTGGCCCACGAACTGGCTGAGACTGAGCACGGGAACACGGTGTTGAGGCACAACATCGAGCGCA A G ODF2 Ensembl:ENSG00000136811 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128471268..128471504 26863196 MeRIP-seq:(Medium) rs751648516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847691,Human_RBP_ID_16584595,Human_RBP_ID_18904172,Human_RBP_ID_26361188 Human_Splice_Rec_1086197,Human_Splice_Rec_1086229,Human_Splice_Rec_1086267,Human_Splice_Rec_1086317,Human_Splice_Rec_1086355,Human_Splice_Rec_1086391,Human_Splice_Rec_1086431,Human_Splice_Rec_1086469,Human_Splice_Rec_1086507,Human_Splice_Rec_1086529,Human_Splice_Rec_1086543,Human_Splice_Rec_1086579,Human_Splice_Rec_1086615 RMVar_hsa_circ_584,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379,RMVar_hsa_circ_74868,RMVar_hsa_circ_259932,RMVar_hsa_circ_34440,RMVar_hsa_circ_377976,RMVar_hsa_circ_329170,RMVar_hsa_circ_259933,RMVar_hsa_circ_354164 107328 RMVar_ID_107328 Human_SNP_ID_415915740 m1A Human chr9 + 128483999 128483999 128483999 TAAATCCATGGAGTCCATGCGTGGGCATTTGCAGGCACAGCTTCGGTCCAAAGAGGCTGAGAACA TAAATCCATGGAGTCCATGCGTGGGCATTTGCGGGCACAGCTTCGGTCCAAAGAGGCTGAGAACA A G ODF2 Ensembl:ENSG00000136811 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128483951..128484000 32194978 MeRIP-seq:(Medium) rs770762208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962699,Human_RBP_ID_5408746,Human_RBP_ID_9407487,Human_RBP_ID_18904177,Human_RBP_ID_26361193,Human_RBP_ID_27833512 Human_Splice_Rec_1086206,Human_Splice_Rec_1086207,Human_Splice_Rec_1086238,Human_Splice_Rec_1086239,Human_Splice_Rec_1086276,Human_Splice_Rec_1086277,Human_Splice_Rec_1086326,Human_Splice_Rec_1086327,Human_Splice_Rec_1086364,Human_Splice_Rec_1086365,Human_Splice_Rec_1086400,Human_Splice_Rec_1086401,Human_Splice_Rec_1086440,Human_Splice_Rec_1086441,Human_Splice_Rec_1086478,Human_Splice_Rec_1086479,Human_Splice_Rec_1086516,Human_Splice_Rec_1086517,Human_Splice_Rec_1086552,Human_Splice_Rec_1086553,Human_Splice_Rec_1086588,Human_Splice_Rec_1086589,Human_Splice_Rec_1086624,Human_Splice_Rec_1086625 RMVar_hsa_circ_584,RMVar_hsa_circ_268379,RMVar_hsa_circ_34440,RMVar_hsa_circ_7663,RMVar_hsa_circ_344422,RMVar_hsa_circ_259935,RMVar_hsa_circ_259936,RMVar_hsa_circ_124566,RMVar_hsa_circ_363630 107329 RMVar_ID_107329 Human_SNP_ID_415915992 m1A Human chr9 - 128484902 128484902 128484902 CAGCCCTCCTCAGGGCAGGTGAGGAGCTGGGCACCGCGGGCCTGCGACCTTGTCAGCGAGTTGCA CAGCCCTCCTCAGGGCAGGTGAGGAGCTGGGCGCCGCGGGCCTGCGACCTTGTCAGCGAGTTGCA T C RF00017-4503,lnc-WDR34-3-001 RNACentral:URS0000948B80,RNACentral:URS00008B53CD SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128484895..128484961 26863196 MeRIP-seq:(Medium) rs1360242666 Functional Loss SNV dbSNP153 33..33 33 - - - 107330 RMVar_ID_107330 Human_SNP_ID_415918313 m1A Human chr9 - 128494557 128494557 128494557 GCCAGCTTCGCCTCCGTGATCTTCAGGATGTCAGGGAGCTGCTGCAGGTCAGCCAGCTGAGACTG GCCAGCTTCGCCTCCGTGATCTTCAGGATGTCTGGGAGCTGCTGCAGGTCAGCCAGCTGAGACTG T A RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128492771..128494725 32194978 MeRIP-seq:(Medium) rs950447419 Functional Loss SNV dbSNP153 33..33 33 - - - 107331 RMVar_ID_107331 Human_SNP_ID_415919462 m1A Human chr9 + 128498549 128498549 128498549 GGGAATGTGGGACCCTGGCAAGGCAGTTGGAGAGTGCCATTGAAGATGCGAGGAGGCAGGTCAGT GGGAATGTGGGACCCTGGCAAGGCAGTTGGAGGGTGCCATTGAAGATGCGAGGAGGCAGGTCAGT A G ODF2 Ensembl:ENSG00000136811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:128498401..128498600;chr9:128498384..128498600;chr9:128498383..128498605 26863196 MeRIP-seq:(Medium) rs377143680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407495,Human_RBP_ID_17715914,Human_RBP_ID_19025708,Human_RBP_ID_22629957,Human_RBP_ID_23094839,Human_RBP_ID_26362206 Human_Splice_Rec_1086255,Human_Splice_Rec_1086343,Human_Splice_Rec_1086417,Human_Splice_Rec_1086457,Human_Splice_Rec_1086605,Human_Splice_Rec_1086641,Human_Splice_Rec_1086651,Human_Splice_Rec_1086655 RMVar_hsa_circ_259940,RMVar_hsa_circ_338634 107332 RMVar_ID_107332 Human_SNP_ID_415919573 m1A Human chr9 + 128498971 128498971 128498971 CTTTGCCAAGTGTTCCCCATGTCCGGTAAACCAGTCTCATGTCTGGGCCTTTGAATGTGCAGGTG CTTTGCCAAGTGTTCCCCATGTCCGGTAAACCGGTCTCATGTCTGGGCCTTTGAATGTGCAGGTG A G ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128498967..128499059 26863196 MeRIP-seq:(Medium) rs748866111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259940,RMVar_hsa_circ_338634 107333 RMVar_ID_107333 Human_SNP_ID_415919943 m1A Human chr9 + 128500171 128500171 128500171 AGCATGCAGAACTACGTCCAGTTCCTCAAATCATCATACGCCAACGTGTTTGGGGATGGTCCCTA AGCATGCAGAACTACGTCCAGTTCCTCAAATCGTCATACGCCAACGTGTTTGGGGATGGTCCCTA A G ODF2 Ensembl:ENSG00000136811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128500121..128500208 26863196 MeRIP-seq:(Medium) rs1329805687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5011327,Human_RBP_ID_17435594 RMVar_hsa_circ_90996,RMVar_hsa_circ_259941 107334 RMVar_ID_107334 Human_SNP_ID_415921145 m1A Human chr9 - 128504827 128504827 128504827 GTCGGAACTGCGTAGGGCCTTCAAGGTCTCCCAGCAGCGACCCTCAGACGGCATGGTTGGCTAAG GTCGGAACTGCGTAGGGCCTTCAAGGTCTCCCTGCAGCGACCCTCAGACGGCATGGTTGGCTAAG T A RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128504776..128504875 26863196 MeRIP-seq:(Medium) rs1238979734 Functional Loss SNV dbSNP153 33..33 33 - - - 107335 RMVar_ID_107335 Human_SNP_ID_415926097 m1A Human chr9 - 128523328 128523328 128523328 CAATTCTGCCAGGCTCTGACCTTTGCTCTGTGACGGTGCTCAGCTTTTAGCTTCTCTTGGTGTCC CAATTCTGCCAGGCTCTGACCTTTGCTCTGTGTCGGTGCTCAGCTTTTAGCTTCTCTTGGTGTCC T A RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128523264..128523357 26863196 MeRIP-seq:(Medium) rs775371645 Functional Loss SNV dbSNP153 33..33 33 - - - 107336 RMVar_ID_107336 Human_SNP_ID_415926098 m1A Human chr9 - 128523328 128523328 128523328 CAATTCTGCCAGGCTCTGACCTTTGCTCTGTGACGGTGCTCAGCTTTTAGCTTCTCTTGGTGTCC CAATTCTGCCAGGCTCTGACCTTTGCTCTGTGGCGGTGCTCAGCTTTTAGCTTCTCTTGGTGTCC T C RF00017-4503 RNACentral:URS0000948B80 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128523264..128523357 26863196 MeRIP-seq:(Medium) rs775371645 Functional Loss SNV dbSNP153 33..33 33 - - - 107337 RMVar_ID_107337 Human_SNP_ID_415933476 m1A Human chr9 + 128552652 128552652 128552652 CGGAGGCCGCGGAGGCTCCTCGGTCCTTCAGCACCCCTCGGCCCGACGCACCCACGCCCCTCACC CGGAGGCCGCGGAGGCTCCTCGGTCCTTCAGCGCCCCTCGGCCCGACGCACCCACGCCCCTCACC A G SPTAN1 Ensembl:ENSG00000197694 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr9:128552601..128552798;chr9:128552601..128552758;chr9:128552601..128552804;chr9:128552601..128552763;chr9:128552601..128553112;chr9:128552601..128553171;chr9:128552601..128552938;chr9:128552601..128552746 26863196 MeRIP-seq:(Medium) rs1380182824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91970,Human_RBP_ID_5035900,Human_RBP_ID_5535495,Human_RBP_ID_9315215,Human_RBP_ID_27130925 Human_Splice_Rec_1086739,Human_Splice_Rec_1086845,Human_Splice_Rec_1086951,Human_Splice_Rec_1087059,Human_Splice_Rec_1087067,Human_Splice_Rec_1087111,Human_Splice_Rec_1087215 Human_miRNA_ID_2153253,Human_miRNA_ID_2801128,Human_miRNA_ID_3009256 RMVar_hsa_circ_259967,RMVar_hsa_circ_89021,RMVar_hsa_circ_122466,RMVar_hsa_circ_105437,RMVar_hsa_circ_259968,RMVar_hsa_circ_259969 107338 RMVar_ID_107338 Human_SNP_ID_415933669 m1A Human chr9 - 128553162 128553162 128553162 CCGGGCTCTTCCTCCCTCTACGGCTGGCCGGCATTGCTGGTGCGATTCGGAAGAACGAGCTGCAG CCGGGCTCTTCCTCCCTCTACGGCTGGCCGGCGTTGCTGGTGCGATTCGGAAGAACGAGCTGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128552657..128553269 32194978 MeRIP-seq:(Medium) rs1349777268 Functional Loss SNV dbSNP153 33..33 33 - - - 107339 RMVar_ID_107339 Human_SNP_ID_415937492 m1A Human chr9 - 128566698 128566698 128566698 GACAAAATGCGCTGAGATAAGTACCAATAGGCACCAAAATAGATGAAAAGTAATTAGCCTCTCTG GACAAAATGCGCTGAGATAAGTACCAATAGGCGCCAAAATAGATGAAAAGTAATTAGCCTCTCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128566696..128566800 26863196 MeRIP-seq:(Medium) rs763542381 Functional Loss SNV dbSNP153 33..33 33 - - - 107340 RMVar_ID_107340 Human_SNP_ID_415940064 m1A Human chr9 - 128577132 128577132 128577132 TTTTCCTTAATCCAACTGATAGTCTCATCCACATCCCTACAGAACAAAGGCACCAGTTAATCCAC TTTTCCTTAATCCAACTGATAGTCTCATCCACGTCCCTACAGAACAAAGGCACCAGTTAATCCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128577126..128577175 26863196 MeRIP-seq:(Medium) rs772435490 Functional Loss SNV dbSNP153 33..33 33 - - - 107341 RMVar_ID_107341 Human_SNP_ID_415941966 m1A Human chr9 + 128584397 128584395 128584398 GGAAGCCCTCGTGGCTCGCTATGAGGCACTCAAGGAGCCCATGGTTGCCCGGAAGCAGAAGCTGG GGAAGCCCTCGTGGCTCGCTATGAGGCACTC___GAGCCCATGGTTGCCCGGAAGCAGAAGCTGG CAAG C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1554746442 Functional Loss DEL dbSNP153 32..34 33 - - - 107342 RMVar_ID_107342 Human_SNP_ID_415941967 m1A Human chr9 + 128584397 128584397 128584397 GGAAGCCCTCGTGGCTCGCTATGAGGCACTCAAGGAGCCCATGGTTGCCCGGAAGCAGAAGCTGG GGAAGCCCTCGTGGCTCGCTATGAGGCACTCAGGGAGCCCATGGTTGCCCGGAAGCAGAAGCTGG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs988580758 Functional Loss SNV dbSNP153 33..33 33 - - - 107343 RMVar_ID_107343 Human_SNP_ID_415943275 m1A Human chr9 - 128588859 128588859 128588859 TCTCGGGGACTCTTCTCCTGATAGTCGTAGAGAGCCAAGACCAGCTCCTTCCCAGTCTCATCATC TCTCGGGGACTCTTCTCCTGATAGTCGTAGAGGGCCAAGACCAGCTCCTTCCCAGTCTCATCATC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128583851..128593002 32194978 MeRIP-seq:(Medium) rs751671825 Functional Loss SNV dbSNP153 33..33 33 - - - 107344 RMVar_ID_107344 Human_SNP_ID_415944065 m1A Human chr9 + 128591535 128591535 128591535 TCGTCAGGGTTTTGTGCCGGCTGCGTACGTGAAGAAATTGGACCCCGCCCAGTCAGCCTCCCGGG TCGTCAGGGTTTTGTGCCGGCTGCGTACGTGACGAAATTGGACCCCGCCCAGTCAGCCTCCCGGG A C SPTAN1 Ensembl:ENSG00000197694 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128591454..128591626 26863196 MeRIP-seq:(Medium) rs1259459718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92005,Human_RBP_ID_798094,Human_RBP_ID_846807,Human_RBP_ID_965001,Human_RBP_ID_8239253,Human_RBP_ID_9315650,Human_RBP_ID_9407545,Human_RBP_ID_22466600,Human_RBP_ID_24549831,Human_RBP_ID_26360499 Human_Splice_Rec_1086777,Human_Splice_Rec_1086883,Human_Splice_Rec_1086989,Human_Splice_Rec_1087105,Human_Splice_Rec_1087149,Human_Splice_Rec_1087257,Human_Splice_Rec_1087323,Human_Splice_Rec_1087401 Human_miRNA_ID_2146578,Human_miRNA_ID_2988002,Human_miRNA_ID_3021701 RMVar_hsa_circ_118614,RMVar_hsa_circ_89021,RMVar_hsa_circ_122466,RMVar_hsa_circ_259968,RMVar_hsa_circ_259969,RMVar_hsa_circ_259970,RMVar_hsa_circ_80231,RMVar_hsa_circ_372712,RMVar_hsa_circ_4626,RMVar_hsa_circ_259972,RMVar_hsa_circ_91821,RMVar_hsa_circ_259973,RMVar_hsa_circ_259975,RMVar_hsa_circ_107871,RMVar_hsa_circ_104104,RMVar_hsa_circ_31877,RMVar_hsa_circ_112148,RMVar_hsa_circ_259979,RMVar_hsa_circ_259978,RMVar_hsa_circ_49456,RMVar_hsa_circ_23303,RMVar_hsa_circ_45531,RMVar_hsa_circ_85199,RMVar_hsa_circ_103691,RMVar_hsa_circ_259981,RMVar_hsa_circ_259982,RMVar_hsa_circ_102712,RMVar_hsa_circ_58730,RMVar_hsa_circ_259984,RMVar_hsa_circ_66432,RMVar_hsa_circ_259985,RMVar_hsa_circ_259983,RMVar_hsa_circ_375466,RMVar_hsa_circ_17946,RMVar_hsa_circ_259987,RMVar_hsa_circ_124153,RMVar_hsa_circ_108877,RMVar_hsa_circ_259988,RMVar_hsa_circ_314577,RMVar_hsa_circ_328669,RMVar_hsa_circ_378128,RMVar_hsa_circ_40712,RMVar_hsa_circ_259992,RMVar_hsa_circ_54178,RMVar_hsa_circ_259991 107345 RMVar_ID_107345 Human_SNP_ID_415947822 m1A Human chr9 + 128605355 128605355 128605355 CGCCTGATCCAGTCCCATCCCGAGTCAGCAGAAGACCTGCAGGAAAAGTGCACAGAGTTAAACCA CGCCTGATCCAGTCCCATCCCGAGTCAGCAGATGACCTGCAGGAAAAGTGCACAGAGTTAAACCA A T SPTAN1 Ensembl:ENSG00000197694 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128605297..128605368 26863196 MeRIP-seq:(Medium) rs1220261648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1070725,Human_RBP_ID_8239260,Human_RBP_ID_9407561,Human_RBP_ID_22466605 Human_Splice_Rec_1086794,Human_Splice_Rec_1086898,Human_Splice_Rec_1087006,Human_Splice_Rec_1087164,Human_Splice_Rec_1087272,Human_Splice_Rec_1087340,Human_Splice_Rec_1087424 RMVar_hsa_circ_655,RMVar_hsa_circ_118614,RMVar_hsa_circ_122466,RMVar_hsa_circ_259969,RMVar_hsa_circ_4626,RMVar_hsa_circ_91821,RMVar_hsa_circ_259973,RMVar_hsa_circ_259975,RMVar_hsa_circ_104104,RMVar_hsa_circ_112148,RMVar_hsa_circ_259978,RMVar_hsa_circ_49456,RMVar_hsa_circ_45531,RMVar_hsa_circ_85199,RMVar_hsa_circ_103691,RMVar_hsa_circ_259982,RMVar_hsa_circ_102712,RMVar_hsa_circ_259984,RMVar_hsa_circ_259985,RMVar_hsa_circ_259983,RMVar_hsa_circ_124153,RMVar_hsa_circ_108877,RMVar_hsa_circ_259988,RMVar_hsa_circ_328669,RMVar_hsa_circ_378128,RMVar_hsa_circ_40712,RMVar_hsa_circ_259991,RMVar_hsa_circ_39558,RMVar_hsa_circ_265890,RMVar_hsa_circ_259998,RMVar_hsa_circ_78154,RMVar_hsa_circ_108838,RMVar_hsa_circ_118989,RMVar_hsa_circ_259995,RMVar_hsa_circ_311123,RMVar_hsa_circ_103220,RMVar_hsa_circ_259994,RMVar_hsa_circ_273190,RMVar_hsa_circ_372797,RMVar_hsa_circ_375329,RMVar_hsa_circ_375972,RMVar_hsa_circ_123195,RMVar_hsa_circ_116259,RMVar_hsa_circ_116737,RMVar_hsa_circ_112175,RMVar_hsa_circ_90880,RMVar_hsa_circ_100325,RMVar_hsa_circ_106126,RMVar_hsa_circ_98058,RMVar_hsa_circ_89168,RMVar_hsa_circ_82126,RMVar_hsa_circ_260002,RMVar_hsa_circ_260006,RMVar_hsa_circ_260010,RMVar_hsa_circ_260012,RMVar_hsa_circ_260011,RMVar_hsa_circ_260008,RMVar_hsa_circ_260009,RMVar_hsa_circ_260007,RMVar_hsa_circ_260004,RMVar_hsa_circ_260005,RMVar_hsa_circ_260003,RMVar_hsa_circ_260000,RMVar_hsa_circ_260001,RMVar_hsa_circ_259999,RMVar_hsa_circ_30157,RMVar_hsa_circ_259996,RMVar_hsa_circ_259997,RMVar_hsa_circ_268421,RMVar_hsa_circ_274101,RMVar_hsa_circ_115694,RMVar_hsa_circ_260016,RMVar_hsa_circ_260017,RMVar_hsa_circ_260015,RMVar_hsa_circ_282609,RMVar_hsa_circ_3942,RMVar_hsa_circ_351969,RMVar_hsa_circ_260019,RMVar_hsa_circ_87027,RMVar_hsa_circ_260020 107346 RMVar_ID_107346 Human_SNP_ID_415949018 m1A Human chr9 - 128609226 128609226 128609226 ACTCATCACTCGCTGTTTGCAATTTTTCACTGATCCAAGCCTCAATCTCATCCACATCCCGGCTG ACTCATCACTCGCTGTTTGCAATTTTTCACTGCTCCAAGCCTCAATCTCATCCACATCCCGGCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128609176..128609316 26863196 MeRIP-seq:(Medium) rs766922699 Functional Loss SNV dbSNP153 33..33 33 - - - 107347 RMVar_ID_107347 Human_SNP_ID_415949030 m1A Human chr9 + 128609265 128609265 128609265 AAAATTGCAAACAGCGAGTGATGAGTCGTACAAGGATCCCACCAACATCCAGGTAAGCTGAAGTG AAAATTGCAAACAGCGAGTGATGAGTCGTACACGGATCCCACCAACATCCAGGTAAGCTGAAGTG A C SPTAN1 Ensembl:ENSG00000197694 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128609214..128609315 32194978 MeRIP-seq:(Medium) rs745319868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92031,Human_RBP_ID_712712,Human_RBP_ID_965020,Human_RBP_ID_1702364,Human_RBP_ID_3190034,Human_RBP_ID_9407580 Human_Splice_Rec_1086805,Human_Splice_Rec_1086909,Human_Splice_Rec_1087017,Human_Splice_Rec_1087175,Human_Splice_Rec_1087351,Human_Splice_Rec_1087439 Human_miRNA_ID_2490249,Human_miRNA_ID_2752329 RMVar_hsa_circ_655,RMVar_hsa_circ_122466,RMVar_hsa_circ_259969,RMVar_hsa_circ_91821,RMVar_hsa_circ_259975,RMVar_hsa_circ_112148,RMVar_hsa_circ_103691,RMVar_hsa_circ_259982,RMVar_hsa_circ_102712,RMVar_hsa_circ_259984,RMVar_hsa_circ_259985,RMVar_hsa_circ_124153,RMVar_hsa_circ_108877,RMVar_hsa_circ_259988,RMVar_hsa_circ_328669,RMVar_hsa_circ_259991,RMVar_hsa_circ_265890,RMVar_hsa_circ_259998,RMVar_hsa_circ_78154,RMVar_hsa_circ_108838,RMVar_hsa_circ_118989,RMVar_hsa_circ_259995,RMVar_hsa_circ_103220,RMVar_hsa_circ_372797,RMVar_hsa_circ_375329,RMVar_hsa_circ_375972,RMVar_hsa_circ_123195,RMVar_hsa_circ_116259,RMVar_hsa_circ_90880,RMVar_hsa_circ_100325,RMVar_hsa_circ_106126,RMVar_hsa_circ_98058,RMVar_hsa_circ_89168,RMVar_hsa_circ_260002,RMVar_hsa_circ_260006,RMVar_hsa_circ_260008,RMVar_hsa_circ_260007,RMVar_hsa_circ_260004,RMVar_hsa_circ_260005,RMVar_hsa_circ_260003,RMVar_hsa_circ_260000,RMVar_hsa_circ_260001,RMVar_hsa_circ_259999,RMVar_hsa_circ_59276,RMVar_hsa_circ_30157,RMVar_hsa_circ_259996,RMVar_hsa_circ_259997,RMVar_hsa_circ_268421,RMVar_hsa_circ_115694,RMVar_hsa_circ_260016,RMVar_hsa_circ_260015,RMVar_hsa_circ_9331,RMVar_hsa_circ_87027,RMVar_hsa_circ_326106,RMVar_hsa_circ_260020,RMVar_hsa_circ_329104,RMVar_hsa_circ_285955,RMVar_hsa_circ_260022,RMVar_hsa_circ_260023,RMVar_hsa_circ_260021,RMVar_hsa_circ_68762,RMVar_hsa_circ_92199,RMVar_hsa_circ_119941,RMVar_hsa_circ_328936,RMVar_hsa_circ_358087,RMVar_hsa_circ_108900,RMVar_hsa_circ_76027,RMVar_hsa_circ_260027,RMVar_hsa_circ_3237,RMVar_hsa_circ_260029,RMVar_hsa_circ_260028,RMVar_hsa_circ_260025,RMVar_hsa_circ_260026,RMVar_hsa_circ_260024 107348 RMVar_ID_107348 Human_SNP_ID_415949543 m1A Human chr9 - 128611667 128611667 128611667 AAAATTTTTTCCAAACCAGTTCCTGCTAGGTTATGTCTTTTCAGGGGGAAGGGGTTCTCAGAGGC AAAATTTTTTCCAAACCAGTTCCTGCTAGGTTCTGTCTTTTCAGGGGGAAGGGGTTCTCAGAGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128611664..128611793 26863196 MeRIP-seq:(Medium) rs1475486374 Functional Loss SNV dbSNP153 33..33 33 - - - 107349 RMVar_ID_107349 Human_SNP_ID_415953295 m1A Human chr9 - 128625515 128625514 128625515 TCCCGCCCCAGGGATCCCTGCCAGCTCTGCCCAGAACACTCGCCCTGCCTCTCTCCCTGACCGTT TCCCGCCCCAGGGATCCCTGCCAGCTCTGCCC_GAACACTCGCCCTGCCTCTCTCCCTGACCGTT CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128625401..128625675 26863196 MeRIP-seq:(Medium) rs527909305 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_27542503 107350 RMVar_ID_107350 Human_SNP_ID_415953367 m1A Human chr9 - 128625776 128625776 128625776 CTTCCTGCTGGAAGGCCTGCAGCCCAGCGTCAAAAGTTTCCTGAACAAGGAGTGACAAGCCAATT CTTCCTGCTGGAAGGCCTGCAGCCCAGCGTCAGAAGTTTCCTGAACAAGGAGTGACAAGCCAATT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128625136..128625826 32194978 MeRIP-seq:(Medium) rs1485892769 Functional Loss SNV dbSNP153 33..33 33 - - - 107351 RMVar_ID_107351 Human_SNP_ID_415953419 m1A Human chr9 - 128625907 128625907 128625907 GCGGGCGGCTGAGTTGGCCAGAAGCTGGCTCCACCTCTTCATGAGGGAGGCGTGCCGGGCCTCGA GCGGGCGGCTGAGTTGGCCAGAAGCTGGCTCCCCCTCTTCATGAGGGAGGCGTGCCGGGCCTCGA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128625858..128626000 26863196 MeRIP-seq:(Medium) rs766038302 Functional Loss SNV dbSNP153 33..33 33 - - - 107352 RMVar_ID_107352 Human_SNP_ID_415953588 m1A Human chr9 - 128626510 128626510 128626510 GAGGAGCGGAAGGCGTCGTGGGCCTCGCGCAAAGCTTTGATTTCTTCCAAGGAGTTGCAGCGCAC GAGGAGCGGAAGGCGTCGTGGGCCTCGCGCAAGGCTTTGATTTCTTCCAAGGAGTTGCAGCGCAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr9:128626376..128626723;chr9:128626357..128626700;chr9:128626346..128626675;chr9:128626451..128626600 26863196 MeRIP-seq:(Medium) rs1564316704 Functional Loss SNV dbSNP153 33..33 33 - - - 107353 RMVar_ID_107353 Human_SNP_ID_415954266 m1A Human chr9 + 128628457 128628455 128628457 GAGGCTGCCACTTTACTTTCCTGGGGTCAGGGAGGGTAACAAGACTGTCCGCCCTAATAGAAGGC GAGGCTGCCACTTTACTTTCCTGGGGTCAGG__GGGTAACAAGACTGTCCGCCCTAATAGAAGGC GGA G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128628407..128628495 26863196 MeRIP-seq:(Medium) rs1564321982 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_92063,Human_RBP_ID_256412,Human_RBP_ID_21690814 RMVar_hsa_circ_122466,RMVar_hsa_circ_259969,RMVar_hsa_circ_112148,RMVar_hsa_circ_103691,RMVar_hsa_circ_259982,RMVar_hsa_circ_102712,RMVar_hsa_circ_259984,RMVar_hsa_circ_259985,RMVar_hsa_circ_124153,RMVar_hsa_circ_259988,RMVar_hsa_circ_259998,RMVar_hsa_circ_259995,RMVar_hsa_circ_103220,RMVar_hsa_circ_90880,RMVar_hsa_circ_100325,RMVar_hsa_circ_98058,RMVar_hsa_circ_259996,RMVar_hsa_circ_259997,RMVar_hsa_circ_115694,RMVar_hsa_circ_260015,RMVar_hsa_circ_87027,RMVar_hsa_circ_260020,RMVar_hsa_circ_92199,RMVar_hsa_circ_260024,RMVar_hsa_circ_260031,RMVar_hsa_circ_108522,RMVar_hsa_circ_126480,RMVar_hsa_circ_260037,RMVar_hsa_circ_90000,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_324017 107354 RMVar_ID_107354 Human_SNP_ID_415955602 m1A Human chr9 - 128632933 128632933 128632933 AGGCCCATACCTGGTAGAGCTCCTCCTTGGTCACGTAAGGCTTTCCCTCTGAGCTGAGGGCCCGG AGGCCCATACCTGGTAGAGCTCCTCCTTGGTCGCGTAAGGCTTTCCCTCTGAGCTGAGGGCCCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128632882..128632957 26863196 MeRIP-seq:(Medium) rs148173166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16585620,Human_RBP_ID_22335873 107355 RMVar_ID_107355 Human_SNP_ID_415955803 m1A Human chr9 - 128633321 128633321 128633321 GGGTGACCCAGGGAGTGGCTCAGTTCACGAAAAGCGAGCGGGTGAACTCCACGTAGTCGAACGCG GGGTGACCCAGGGAGTGGCTCAGTTCACGAAACGCGAGCGGGTGAACTCCACGTAGTCGAACGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128633270..128633381 26863196 MeRIP-seq:(Medium) rs1287446335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900900 107356 RMVar_ID_107356 Human_SNP_ID_415955814 m1A Human chr9 - 128633348 128633348 128633348 GGCGACGCAGGGCAAGCAGCGAGGGGTGGGTGACCCAGGGAGTGGCTCAGTTCACGAAAAGCGAG GGCGACGCAGGGCAAGCAGCGAGGGGTGGGTGGCCCAGGGAGTGGCTCAGTTCACGAAAAGCGAG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:128633301..128633375 26863196 MeRIP-seq:(Medium) rs1218770880 Functional Loss SNV dbSNP153 33..33 33 - - - 107357 RMVar_ID_107357 Human_SNP_ID_415956019 m1A Human chr9 - 128633757 128633757 128633757 GGAAGCTGAGGACCTGGACTGCCTGGCAGCAGAGGTGGCGGCCTGAGGGGTCCCGGGAGGCGGGT GGAAGCTGAGGACCTGGACTGCCTGGCAGCAGCGGTGGCGGCCTGAGGGGTCCCGGGAGGCGGGT T G WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128633706..128633870 26863196 MeRIP-seq:(Medium) rs551915056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712734,Human_RBP_ID_18130349,Human_RBP_ID_26565320,Human_RBP_ID_27542517 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_112052,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260046,RMVar_hsa_circ_260047 107358 RMVar_ID_107358 Human_SNP_ID_415956266 m1A Human chr9 - 128634228 128634228 128634228 GCGGCCCTTGGTTTTTGCAGCTGCCTCTGGGAAAGGTAGGAAGGGGCCGCTAGGCCTGGATCTGT GCGGCCCTTGGTTTTTGCAGCTGCCTCTGGGAGAGGTAGGAAGGGGCCGCTAGGCCTGGATCTGT T C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128634226..128634400 32194978 MeRIP-seq:(Medium) rs1373451193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18172976,Human_RBP_ID_26566016 Human_Splice_Rec_1087539 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260047,RMVar_hsa_circ_98804,RMVar_hsa_circ_260054 107359 RMVar_ID_107359 Human_SNP_ID_415956280 m1A Human chr9 + 128634253 128634253 128634253 CCTACCTTTCCCAGAGGCAGCTGCAAAAACCAAGGGCCGCACTGGGGACCAGCGCACAGCAAACA CCTACCTTTCCCAGAGGCAGCTGCAAAAACCATGGGCCGCACTGGGGACCAGCGCACAGCAAACA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128634226..128634300 26863196 MeRIP-seq:(Medium) rs1404104700 Functional Loss SNV dbSNP153 33..33 33 - - - 107360 RMVar_ID_107360 Human_SNP_ID_415956514 m1A Human chr9 - 128634744 128634744 128634744 GCTCCGTGCCCCTGCGGGCCCCAGCACAGTTTACCTTCTCCCCCCACGGCGGTCCCATCTACTCT GCTCCGTGCCCCTGCGGGCCCCAGCACAGTTTGCCTTCTCCCCCCACGGCGGTCCCATCTACTCT T C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr9:128634657..128634939;chr9:128634654..128634900 26863196 MeRIP-seq:(Medium) rs545458296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5039237,Human_RBP_ID_18130352,Human_RBP_ID_24287872 Human_Splice_Rec_1087537 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_82663,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260047,RMVar_hsa_circ_260055 107361 RMVar_ID_107361 Human_SNP_ID_415956535 m1A Human chr9 - 128634777 128634777 128634777 CAGCTGGAGAGGCAGCCCTCACGCGGATGCCCAGCTCCGTGCCCCTGCGGGCCCCAGCACAGTTT CAGCTGGAGAGGCAGCCCTCACGCGGATGCCCCGCTCCGTGCCCCTGCGGGCCCCAGCACAGTTT T G WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr9:128634676..128634850;chr9:128634726..128634860 26863196 MeRIP-seq:(Medium) rs1167247704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24287872 Human_Splice_Rec_1087537 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_82663,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260047,RMVar_hsa_circ_260055 107362 RMVar_ID_107362 Human_SNP_ID_415956550 m1A Human chr9 - 128634796 128634796 128634796 CCGCTCAAGTGTTCCCTGGCAGCTGGAGAGGCAGCCCTCACGCGGATGCCCAGCTCCGTGCCCCT CCGCTCAAGTGTTCCCTGGCAGCTGGAGAGGCTGCCCTCACGCGGATGCCCAGCTCCGTGCCCCT T A WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128634676..128635116 26863410 MeRIP-seq:(Medium) rs202029061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_82663,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260047,RMVar_hsa_circ_260055 107363 RMVar_ID_107363 Human_SNP_ID_415956552 m1A Human chr9 - 128634800 128634798 128634800 CTTCCCGCTCAAGTGTTCCCTGGCAGCTGGAGAGGCAGCCCTCACGCGGATGCCCAGCTCCGTGC CTTCCCGCTCAAGTGTTCCCTGGCAGCTGGAG__GCAGCCCTCACGCGGATGCCCAGCTCCGTGC CCT C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128634676..128635326 32194978 MeRIP-seq:(Medium) rs759150616 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_121246,RMVar_hsa_circ_103594,RMVar_hsa_circ_95958,RMVar_hsa_circ_82663,RMVar_hsa_circ_260048,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_78755,RMVar_hsa_circ_260051,RMVar_hsa_circ_260049,RMVar_hsa_circ_260047,RMVar_hsa_circ_260055 107364 RMVar_ID_107364 Human_SNP_ID_415956918 m1A Human chr9 + 128635665 128635665 128635665 CCCGCCCGGCAGCCCCTGCCCTGACCTGGGACACAGGGTCTGTGTGGGTGTCATCCGTCAGGCCT CCCGCCCGGCAGCCCCTGCCCTGACCTGGGACGCAGGGTCTGTGTGGGTGTCATCCGTCAGGCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128635651..128635775 32194978 MeRIP-seq:(Medium) rs754488103 Functional Loss SNV dbSNP153 33..33 33 - - - 107365 RMVar_ID_107365 Human_SNP_ID_415956965 m1A Human chr9 + 128635761 128635761 128635761 TCAGGTCCCACACCAACACCTCACCACTGTACAGCCCTCCTGCAGGGACAGTGGACCTGGGCAGA TCAGGTCCCACACCAACACCTCACCACTGTACTGCCCTCCTGCAGGGACAGTGGACCTGGGCAGA A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128635712..128636183 26863196 MeRIP-seq:(Medium) rs374009469 Functional Loss SNV dbSNP153 33..33 33 - - - 107366 RMVar_ID_107366 Human_SNP_ID_415957038 m1A Human chr9 + 128635993 128635993 128635993 ACACCCCTGCCCTGCACCTGGCAGCTCCCTCCAGCGTTGCCTGCCCCCTACCACTGACGGCTTCC ACACCCCTGCCCTGCACCTGGCAGCTCCCTCCCGCGTTGCCTGCCCCCTACCACTGACGGCTTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128635988..128636078 26863196 MeRIP-seq:(Medium) rs1414379241 Functional Loss SNV dbSNP153 33..33 33 - - - 107367 RMVar_ID_107367 Human_SNP_ID_415957231 m1A Human chr9 + 128636411 128636410 128636411 CGGTCCAGGTTCCAGGCACACACGAAGGACTTAAGCGTGCTCCAGTCCCCATGGTCCAGCCTGTG CGGTCCAGGTTCCAGGCACACACGAAGGACTT_AGCGTGCTCCAGTCCCCATGGTCCAGCCTGTG TA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128636259..128636524 26863196 MeRIP-seq:(Medium) rs750708075 Functional Loss DEL dbSNP153 33..33 33 - - - 107368 RMVar_ID_107368 Human_SNP_ID_415957427 m1A Human chr9 - 128637002 128637002 128637002 TCCGCAGGTGTCTTGTCTGTATACCCTGGGCTACCCGCCAGCCCAAGCGCAGGGTCTGCATGTGA TCCGCAGGTGTCTTGTCTGTATACCCTGGGCTGCCCGCCAGCCCAAGCGCAGGGTCTGCATGTGA T C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128636951..128637050 26863196 MeRIP-seq:(Medium) rs141038992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712756,Human_RBP_ID_1058061,Human_RBP_ID_1118269,Human_RBP_ID_1402578,Human_RBP_ID_16585638,Human_RBP_ID_27542525,Human_RBP_ID_27570311 Human_Splice_Rec_1087528,Human_Splice_Rec_1087529,Human_Splice_Rec_1087553,Human_Splice_Rec_1087560,Human_Splice_Rec_1087561 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_103594,RMVar_hsa_circ_82663,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_260051,RMVar_hsa_circ_260055 107369 RMVar_ID_107369 Human_SNP_ID_415957429 m1A Human chr9 - 128637014 128637014 128637014 GTTGGGGACGTCTCCGCAGGTGTCTTGTCTGTATACCCTGGGCTACCCGCCAGCCCAAGCGCAGG GTTGGGGACGTCTCCGCAGGTGTCTTGTCTGTTTACCCTGGGCTACCCGCCAGCCCAAGCGCAGG T A WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128636963..128637067 26863196 MeRIP-seq:(Medium) rs1382703162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712756,Human_RBP_ID_1058061,Human_RBP_ID_1118269,Human_RBP_ID_1402578,Human_RBP_ID_16585638,Human_RBP_ID_27370792,Human_RBP_ID_27542525,Human_RBP_ID_27570311 Human_Splice_Rec_1087528,Human_Splice_Rec_1087529,Human_Splice_Rec_1087553,Human_Splice_Rec_1087560,Human_Splice_Rec_1087561 RMVar_hsa_circ_84553,RMVar_hsa_circ_100759,RMVar_hsa_circ_103594,RMVar_hsa_circ_82663,RMVar_hsa_circ_260050,RMVar_hsa_circ_260052,RMVar_hsa_circ_260051,RMVar_hsa_circ_260055 107370 RMVar_ID_107370 Human_SNP_ID_415962957 m1A Human chr9 - 128656560 128656560 128656560 GGCGTCCGTGCCCTCGCAGTGGAGGGCCGTCCAGGGCATCCGCTGGGAGACGGTGAGGGCGCGGG GGCGTCCGTGCCCTCGCAGTGGAGGGCCGTCCGGGGCATCCGCTGGGAGACGGTGAGGGCGCGGG T C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128640726..128656700 26863196 MeRIP-seq:(Medium) rs750192253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035905,Human_RBP_ID_8944646,Human_RBP_ID_17175277,Human_RBP_ID_18427226 Human_Splice_Rec_1087525,Human_Splice_Rec_1087545,Human_Splice_Rec_1087557,Human_Splice_Rec_1087563 Human_miRNA_ID_2509152,Human_miRNA_ID_3090419 RMVar_hsa_circ_103594,RMVar_hsa_circ_260052 107371 RMVar_ID_107371 Human_SNP_ID_415970912 m1A Human chr9 - 128683897 128683897 128683897 GAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCATGCTGTTAGGGAAGTCCCAGAACCAGACCACG GAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCTTGCTGTTAGGGAAGTCCCAGAACCAGACCACG T A HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128683459..128684045 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_16586200 107372 RMVar_ID_107372 Human_SNP_ID_415970913 m1A Human chr9 - 128683897 128683897 128683897 GAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCATGCTGTTAGGGAAGTCCCAGAACCAGACCACG GAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCCTGCTGTTAGGGAAGTCCCAGAACCAGACCACG T G HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128683459..128684045 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_16586200 107373 RMVar_ID_107373 Human_SNP_ID_415970919 m1A Human chr9 - 128683904 128683904 128683904 TTCTTTTGAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCATGCTGTTAGGGAAGTCCCAGAACCA TTCTTTTGAGGCGGGAGTGGAGACTGGCGTTTCGGGGCCATGCTGTTAGGGAAGTCCCAGAACCA T G HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128683476..128684033 26863196 MeRIP-seq:(Medium) rs1237335688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16586201 107374 RMVar_ID_107374 Human_SNP_ID_415970924 m1A Human chr9 - 128683921 128683921 128683921 GAGGTGGTCTTGGTTTCTTCTTTTGAGGCGGGAGTGGAGACTGGCGTTTAGGGGCCATGCTGTTA GAGGTGGTCTTGGTTTCTTCTTTTGAGGCGGGGGTGGAGACTGGCGTTTAGGGGCCATGCTGTTA T C HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128683873..128684004 26863196 MeRIP-seq:(Medium) rs1180724092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900946 107375 RMVar_ID_107375 Human_SNP_ID_415972615 m1A Human chr9 + 128689425 128689421 128689425 CTCGGCGTCAGGCCGCGAGGGTAGCGCGCGCGAGCGAGCGAGGGGGAGGGAGAGCGAGCGAGCGC CTCGGCGTCAGGCCGCGAGGGTAGCGCGC____GCGAGCGAGGGGGAGGGAGAGCGAGCGAGCGC CGCGA C SET Ensembl:ENSG00000119335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:128689201..128689707;chr9:128689201..128689680;chr9:128689201..128690019 26863196 MeRIP-seq:(Medium) rs953279378 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_256594,Human_RBP_ID_798189,Human_RBP_ID_5011858,Human_RBP_ID_5124036,Human_RBP_ID_7900952,Human_RBP_ID_8275124,Human_RBP_ID_9339092,Human_RBP_ID_9407604,Human_RBP_ID_22467107,Human_RBP_ID_22534474,Human_RBP_ID_22628509,Human_RBP_ID_23141369,Human_RBP_ID_27131081,Human_RBP_ID_27833526 107376 RMVar_ID_107376 Human_SNP_ID_415972622 m1A Human chr9 + 128689439 128689439 128689439 GCGAGGGTAGCGCGCGCGAGCGAGCGAGGGGGAGGGAGAGCGAGCGAGCGCCGGGAGGAGGCGGC GCGAGGGTAGCGCGCGCGAGCGAGCGAGGGGGGGGGAGAGCGAGCGAGCGCCGGGAGGAGGCGGC A G SET Ensembl:ENSG00000119335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128689201..128689687 26863196 MeRIP-seq:(Medium) rs939257924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256594,Human_RBP_ID_798189,Human_RBP_ID_5011858,Human_RBP_ID_7900952,Human_RBP_ID_8275124,Human_RBP_ID_9339092,Human_RBP_ID_9407604,Human_RBP_ID_22467107,Human_RBP_ID_22534502,Human_RBP_ID_22628509,Human_RBP_ID_23141369,Human_RBP_ID_27131081 107377 RMVar_ID_107377 Human_SNP_ID_415972646 m1A Human chr9 - 128689495 128689495 128689495 GGGGGCGGGCAAGCGGCTTCCCCTCACGCCACACGCGCGGGCGCCCGCTCGGTCCGGCCGCCTCC GGGGGCGGGCAAGCGGCTTCCCCTCACGCCACGCGCGCGGGCGCCCGCTCGGTCCGGCCGCCTCC T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr9:128689226..128689600;chr9:128689251..128689559 26863410 MeRIP-seq:(Medium) rs1162876934 Functional Loss SNV dbSNP153 33..33 33 - - - 107378 RMVar_ID_107378 Human_SNP_ID_415972658 m1A Human chr9 - 128689535 128689535 128689535 TCGGGGGGGGAGCGGGGAGGGGGAGAGAAGGGAAGGCGAAGGGGGCGGGCAAGCGGCTTCCCCTC TCGGGGGGGGAGCGGGGAGGGGGAGAGAAGGGCAGGCGAAGGGGGCGGGCAAGCGGCTTCCCCTC T G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:128689226..128689705 26863196 MeRIP-seq:(Medium) rs1400160989 Functional Loss SNV dbSNP153 33..33 33 - - - 107379 RMVar_ID_107379 Human_SNP_ID_415972663 m1A Human chr9 - 128689539 128689539 128689539 GCGGTCGGGGGGGGAGCGGGGAGGGGGAGAGAAGGGAAGGCGAAGGGGGCGGGCAAGCGGCTTCC GCGGTCGGGGGGGGAGCGGGGAGGGGGAGAGACGGGAAGGCGAAGGGGGCGGGCAAGCGGCTTCC T G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:128689276..128690019;chr9:128689276..128689625 32194978 MeRIP-seq:(Medium) rs1028771744 Functional Loss SNV dbSNP153 33..33 33 - - - 107380 RMVar_ID_107380 Human_SNP_ID_415972664 m1A Human chr9 - 128689540 128689540 128689540 CGCGGTCGGGGGGGGAGCGGGGAGGGGGAGAGAAGGGAAGGCGAAGGGGGCGGGCAAGCGGCTTC CGCGGTCGGGGGGGGAGCGGGGAGGGGGAGAGTAGGGAAGGCGAAGGGGGCGGGCAAGCGGCTTC T A RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128689251..128690292 26863410 MeRIP-seq:(Medium) rs745748421 Functional Loss SNV dbSNP153 33..33 33 - - - 107381 RMVar_ID_107381 Human_SNP_ID_415973742 m1A Human chr9 - 128691854 128691854 128691854 AAATCTCCTCACTGGCTTGTTCATTAAGTCTGAAGCAAATGAAAAGAGATGTTGACAATGATAGT AAATCTCCTCACTGGCTTGTTCATTAAGTCTGGAGCAAATGAAAAGAGATGTTGACAATGATAGT T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr9:128691851..128691900 26863196,32194978 MeRIP-seq:(Medium) rs772579604 Functional Loss SNV dbSNP153 33..33 33 - - - 107382 RMVar_ID_107382 Human_SNP_ID_415973743 m1A Human chr9 - 128691854 128691854 128691854 AAATCTCCTCACTGGCTTGTTCATTAAGTCTGAAGCAAATGAAAAGAGATGTTGACAATGATAGT AAATCTCCTCACTGGCTTGTTCATTAAGTCTGCAGCAAATGAAAAGAGATGTTGACAATGATAGT T G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr9:128691851..128691900 26863196,32194978 MeRIP-seq:(Medium) rs772579604 Functional Loss SNV dbSNP153 33..33 33 - - - 107383 RMVar_ID_107383 Human_SNP_ID_415974402 m1A Human chr9 - 128693622 128693622 128693622 GAACGTTTCGTCAAATCCTAAATGAATACCGGAAGAGCTTTTGATACAATCTCTCCATAACACCC GAACGTTTCGTCAAATCCTAAATGAATACCGGGAGAGCTTTTGATACAATCTCTCCATAACACCC T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128693621..128693695 26863196 MeRIP-seq:(Medium) rs1407654947 Functional Loss SNV dbSNP153 33..33 33 - - - 107384 RMVar_ID_107384 Human_SNP_ID_415974540 m1A Human chr9 + 128693978 128693976 128693979 TGATGAAGAGGAGGAAGGATTAGAAGATATTGACGAAGAAGGGGATGAGGATGAAGGTGAAGAAG TGATGAAGAGGAGGAAGGATTAGAAGATATT___GAAGAAGGGGATGAGGATGAAGGTGAAGAAG TGAC T SET Ensembl:ENSG00000119335 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:128693815..128694064 26863196 MeRIP-seq:(Medium) rs1194050226 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_90709,Human_RBP_ID_219040,Human_RBP_ID_255848,Human_RBP_ID_712780,Human_RBP_ID_796963,Human_RBP_ID_846952,Human_RBP_ID_965239,Human_RBP_ID_1058069,Human_RBP_ID_1702401,Human_RBP_ID_2061206,Human_RBP_ID_3190146,Human_RBP_ID_3975865,Human_RBP_ID_5011887,Human_RBP_ID_5227127,Human_RBP_ID_5637075,Human_RBP_ID_7900977,Human_RBP_ID_8275126,Human_RBP_ID_8697482,Human_RBP_ID_8925605,Human_RBP_ID_9233311,Human_RBP_ID_9407614,Human_RBP_ID_10441513,Human_RBP_ID_16586291,Human_RBP_ID_17715941,Human_RBP_ID_18140668,Human_RBP_ID_18542447,Human_RBP_ID_18904287,Human_RBP_ID_21691002,Human_RBP_ID_22118893,Human_RBP_ID_22335924,Human_RBP_ID_22517816,Human_RBP_ID_22837782,Human_RBP_ID_23094401,Human_RBP_ID_23117234,Human_RBP_ID_23120865,Human_RBP_ID_23200283,Human_RBP_ID_24287929,Human_RBP_ID_24522387,Human_RBP_ID_24549666,Human_RBP_ID_26241763,Human_RBP_ID_26360516,Human_RBP_ID_26566568,Human_RBP_ID_27131104,Human_RBP_ID_27370807,Human_RBP_ID_27542532,Human_RBP_ID_27832811 Human_Splice_Rec_1087586,Human_Splice_Rec_1087587,Human_Splice_Rec_1087600,Human_Splice_Rec_1087601,Human_Splice_Rec_1087614,Human_Splice_Rec_1087615,Human_Splice_Rec_1087628,Human_Splice_Rec_1087629,Human_Splice_Rec_1087642,Human_Splice_Rec_1087643,Human_Splice_Rec_1087660 RMVar_hsa_circ_260064,RMVar_hsa_circ_76862,RMVar_hsa_circ_112044,RMVar_hsa_circ_365387,RMVar_hsa_circ_260058,RMVar_hsa_circ_122060,RMVar_hsa_circ_260059,RMVar_hsa_circ_100662,RMVar_hsa_circ_81778,RMVar_hsa_circ_260060,RMVar_hsa_circ_102041,RMVar_hsa_circ_260061,RMVar_hsa_circ_110943,RMVar_hsa_circ_260062,RMVar_hsa_circ_260063,RMVar_hsa_circ_120725,RMVar_hsa_circ_260065,RMVar_hsa_circ_260066,RMVar_hsa_circ_109265,RMVar_hsa_circ_260068,RMVar_hsa_circ_260067,RMVar_hsa_circ_376959,RMVar_hsa_circ_378170 107385 RMVar_ID_107385 Human_SNP_ID_415974541 m1A Human chr9 + 128693982 128693979 128693982 GAAGAGGAGGAAGGATTAGAAGATATTGACGAAGAAGGGGATGAGGATGAAGGTGAAGAAGATGA GAAGAGGAGGAAGGATTAGAAGATATTGAC___GAAGGGGATGAGGATGAAGGTGAAGAAGATGA CGAA C SET Ensembl:ENSG00000119335 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128693876..128694707 32194978 MeRIP-seq:(Medium) rs760981674 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_90709,Human_RBP_ID_219040,Human_RBP_ID_255848,Human_RBP_ID_712780,Human_RBP_ID_846952,Human_RBP_ID_965239,Human_RBP_ID_1058069,Human_RBP_ID_1702401,Human_RBP_ID_2061207,Human_RBP_ID_3190148,Human_RBP_ID_3975865,Human_RBP_ID_5227127,Human_RBP_ID_7900977,Human_RBP_ID_8275126,Human_RBP_ID_8697483,Human_RBP_ID_8925605,Human_RBP_ID_9233311,Human_RBP_ID_9407614,Human_RBP_ID_16586291,Human_RBP_ID_18140668,Human_RBP_ID_18542448,Human_RBP_ID_22118893,Human_RBP_ID_22517816,Human_RBP_ID_23094401,Human_RBP_ID_23117234,Human_RBP_ID_23120865,Human_RBP_ID_24287929,Human_RBP_ID_24522387,Human_RBP_ID_24549666,Human_RBP_ID_26360516,Human_RBP_ID_27542532,Human_RBP_ID_27832811 Human_Splice_Rec_1087586,Human_Splice_Rec_1087587,Human_Splice_Rec_1087600,Human_Splice_Rec_1087601,Human_Splice_Rec_1087614,Human_Splice_Rec_1087615,Human_Splice_Rec_1087628,Human_Splice_Rec_1087629,Human_Splice_Rec_1087642,Human_Splice_Rec_1087643,Human_Splice_Rec_1087660 Human_miRNA_ID_550678,Human_miRNA_ID_2195310,Human_miRNA_ID_2195311 RMVar_hsa_circ_260064,RMVar_hsa_circ_76862,RMVar_hsa_circ_112044,RMVar_hsa_circ_365387,RMVar_hsa_circ_260058,RMVar_hsa_circ_122060,RMVar_hsa_circ_260059,RMVar_hsa_circ_100662,RMVar_hsa_circ_81778,RMVar_hsa_circ_260060,RMVar_hsa_circ_102041,RMVar_hsa_circ_260061,RMVar_hsa_circ_110943,RMVar_hsa_circ_260062,RMVar_hsa_circ_260063,RMVar_hsa_circ_120725,RMVar_hsa_circ_260065,RMVar_hsa_circ_260066,RMVar_hsa_circ_109265,RMVar_hsa_circ_260068,RMVar_hsa_circ_260067,RMVar_hsa_circ_376959,RMVar_hsa_circ_378170 107386 RMVar_ID_107386 Human_SNP_ID_415974541 m1A Human chr9 + 128693981 128693979 128693982 TGAAGAGGAGGAAGGATTAGAAGATATTGACGAAGAAGGGGATGAGGATGAAGGTGAAGAAGATG TGAAGAGGAGGAAGGATTAGAAGATATTGAC___GAAGGGGATGAGGATGAAGGTGAAGAAGATG CGAA C SET Ensembl:ENSG00000119335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128693749..128694050;chr9:128693876..128694833;chr9:128693876..128694050;chr9:128693726..128694725 26863196 MeRIP-seq:(Medium) rs760981674 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_90709,Human_RBP_ID_219040,Human_RBP_ID_255848,Human_RBP_ID_712780,Human_RBP_ID_846952,Human_RBP_ID_965239,Human_RBP_ID_1058069,Human_RBP_ID_1702401,Human_RBP_ID_2061206,Human_RBP_ID_3190147,Human_RBP_ID_3975865,Human_RBP_ID_5039276,Human_RBP_ID_5227127,Human_RBP_ID_5637075,Human_RBP_ID_7900977,Human_RBP_ID_8275126,Human_RBP_ID_8697482,Human_RBP_ID_8925605,Human_RBP_ID_9233311,Human_RBP_ID_9407614,Human_RBP_ID_10441513,Human_RBP_ID_16586291,Human_RBP_ID_17715941,Human_RBP_ID_18140668,Human_RBP_ID_18542447,Human_RBP_ID_18904287,Human_RBP_ID_21691002,Human_RBP_ID_22118893,Human_RBP_ID_22335924,Human_RBP_ID_22517816,Human_RBP_ID_22837782,Human_RBP_ID_23094401,Human_RBP_ID_23117234,Human_RBP_ID_23120865,Human_RBP_ID_23200283,Human_RBP_ID_24287929,Human_RBP_ID_24522387,Human_RBP_ID_24549666,Human_RBP_ID_26241763,Human_RBP_ID_26360516,Human_RBP_ID_26566568,Human_RBP_ID_27131104,Human_RBP_ID_27370807,Human_RBP_ID_27542532,Human_RBP_ID_27832811 Human_Splice_Rec_1087586,Human_Splice_Rec_1087587,Human_Splice_Rec_1087600,Human_Splice_Rec_1087601,Human_Splice_Rec_1087614,Human_Splice_Rec_1087615,Human_Splice_Rec_1087628,Human_Splice_Rec_1087629,Human_Splice_Rec_1087642,Human_Splice_Rec_1087643,Human_Splice_Rec_1087660 Human_miRNA_ID_550678,Human_miRNA_ID_2195310,Human_miRNA_ID_2195311 RMVar_hsa_circ_260064,RMVar_hsa_circ_76862,RMVar_hsa_circ_112044,RMVar_hsa_circ_365387,RMVar_hsa_circ_260058,RMVar_hsa_circ_122060,RMVar_hsa_circ_260059,RMVar_hsa_circ_100662,RMVar_hsa_circ_81778,RMVar_hsa_circ_260060,RMVar_hsa_circ_102041,RMVar_hsa_circ_260061,RMVar_hsa_circ_110943,RMVar_hsa_circ_260062,RMVar_hsa_circ_260063,RMVar_hsa_circ_120725,RMVar_hsa_circ_260065,RMVar_hsa_circ_260066,RMVar_hsa_circ_109265,RMVar_hsa_circ_260068,RMVar_hsa_circ_260067,RMVar_hsa_circ_376959,RMVar_hsa_circ_378170 107387 RMVar_ID_107387 Human_SNP_ID_415975215 m1A Human chr9 + 128695801 128695801 128695801 ATTTGGGATACCAGATAGCTCAATACTCTCTGAGTACATTGTGCCCTTGATTTTTATCTCCAAGT ATTTGGGATACCAGATAGCTCAATACTCTCTGCGTACATTGTGCCCTTGATTTTTATCTCCAAGT A C SET Ensembl:ENSG00000119335 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128695751..128695825 32194978 MeRIP-seq:(Medium) rs541691638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712822,Human_RBP_ID_1702419,Human_RBP_ID_2061223,Human_RBP_ID_5271192,Human_RBP_ID_7901041,Human_RBP_ID_8697493,Human_RBP_ID_8925611,Human_RBP_ID_9233323,Human_RBP_ID_9314389,Human_RBP_ID_17321280,Human_RBP_ID_17435613,Human_RBP_ID_17548566,Human_RBP_ID_18130385,Human_RBP_ID_18396300,Human_RBP_ID_26566579,Human_RBP_ID_27131120,Human_RBP_ID_27783327 Human_miRNA_ID_1509737 RMVar_hsa_circ_76862,RMVar_hsa_circ_112044,RMVar_hsa_circ_260058,RMVar_hsa_circ_122060,RMVar_hsa_circ_260059,RMVar_hsa_circ_100662,RMVar_hsa_circ_81778,RMVar_hsa_circ_260060,RMVar_hsa_circ_260061,RMVar_hsa_circ_260063,RMVar_hsa_circ_120725,RMVar_hsa_circ_260065,RMVar_hsa_circ_260066,RMVar_hsa_circ_109265 107388 RMVar_ID_107388 Human_SNP_ID_415977421 m1A Human chr9 - 128702882 128702882 128702882 GCGCCGCTCCGGCCGCTTGGGGCCCTTCTCTCAGCCACTCCGGTCCCGGAAGCCGCAGACCCTCC GCGCCGCTCCGGCCGCTTGGGGCCCTTCTCTCTGCCACTCCGGTCCCGGAAGCCGCAGACCCTCC T A RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128702526..128705466 26863196 MeRIP-seq:(Medium) rs774102826 Functional Loss SNV dbSNP153 33..33 33 - - - 107389 RMVar_ID_107389 Human_SNP_ID_415977422 m1A Human chr9 - 128702882 128702882 128702882 GCGCCGCTCCGGCCGCTTGGGGCCCTTCTCTCAGCCACTCCGGTCCCGGAAGCCGCAGACCCTCC GCGCCGCTCCGGCCGCTTGGGGCCCTTCTCTCGGCCACTCCGGTCCCGGAAGCCGCAGACCCTCC T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128702526..128705466 26863196 MeRIP-seq:(Medium) rs774102826 Functional Loss SNV dbSNP153 33..33 33 - - - 107390 RMVar_ID_107390 Human_SNP_ID_415977933 m1A Human chr9 + 128704425 128704425 128704425 GCCCTGGCTCCCAGGCCCCTGGCTGCCTTCTCATGTGGCTTCGTGTGAACCCCTATTCGGCGTAG GCCCTGGCTCCCAGGCCCCTGGCTGCCTTCTCGTGTGGCTTCGTGTGAACCCCTATTCGGCGTAG A G PKN3 Ensembl:ENSG00000160447 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128704291..128704500 26863196 MeRIP-seq:(Medium) rs1042075101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27131151 107391 RMVar_ID_107391 Human_SNP_ID_415978424 m1A Human chr9 - 128705827 128705827 128705827 ACGTGTGGGTCATGTTCTCAGCCCCCTGCTTCACCTTCAGCTCCACATGCAGCTGCCTCCGGAGA ACGTGTGGGTCATGTTCTCAGCCCCCTGCTTCGCCTTCAGCTCCACATGCAGCTGCCTCCGGAGA T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128705776..128705895 26863196 MeRIP-seq:(Medium) rs1314642092 Functional Loss SNV dbSNP153 33..33 33 - - - 107392 RMVar_ID_107392 Human_SNP_ID_415978797 m1A Human chr9 + 128706968 128706968 128706968 CGTTGAGGCAGCTGTGGCTGAGGGCGCCAAGAACGTGGTGAAACTGCTTAGTAGCCGGAGAACAC CGTTGAGGCAGCTGTGGCTGAGGGCGCCAAGATCGTGGTGAAACTGCTTAGTAGCCGGAGAACAC A T PKN3 Ensembl:ENSG00000160447 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128706848..128706969 26863196 MeRIP-seq:(Medium) rs1352431866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3974898,Human_RBP_ID_23094406 Human_Splice_Rec_1087682,Human_Splice_Rec_1087683 RMVar_hsa_circ_6361,RMVar_hsa_circ_28195,RMVar_hsa_circ_35667 107393 RMVar_ID_107393 Human_SNP_ID_415981034 m1A Human chr9 + 128714350 128714350 128714350 TCGGACCCCAACAACACTGCGAGAGGCCTCTGACCCTGCCACTCCCAGGTGAGGAGCTCCCTTGC TCGGACCCCAACAACACTGCGAGAGGCCTCTGCCCCTGCCACTCCCAGGTGAGGAGCTCCCTTGC A C PKN3 Ensembl:ENSG00000160447 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128714301..128714875 26863196 MeRIP-seq:(Medium) rs770230806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1087695 RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587,RMVar_hsa_circ_46117,RMVar_hsa_circ_13508 107394 RMVar_ID_107394 Human_SNP_ID_415981333 m1A Human chr9 - 128715152 128715152 128715152 CCGAGGGGGTTTCCTGCAAAGGAAGAGAGGGTATATGAAGTCCCCTAGGGCACTGGCTGGGCCCC CCGAGGGGGTTTCCTGCAAAGGAAGAGAGGGTTTATGAAGTCCCCTAGGGCACTGGCTGGGCCCC T A RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128715151..128715200 26863196 MeRIP-seq:(Medium) rs1320443375 Functional Loss SNV dbSNP153 33..33 33 - - - 107395 RMVar_ID_107395 Human_SNP_ID_415981334 m1A Human chr9 + 128715153 128715153 128715153 GGGCCCAGCCAGTGCCCTAGGGGACTTCATATACCCTCTCTTCCTTTGCAGGAAACCCCCTCGGC GGGCCCAGCCAGTGCCCTAGGGGACTTCATATGCCCTCTCTTCCTTTGCAGGAAACCCCCTCGGC A G PKN3 Ensembl:ENSG00000160447 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128715151..128715200 26863196 MeRIP-seq:(Medium) rs762406689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1087701,Human_Splice_Rec_1087729 RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587 107396 RMVar_ID_107396 Human_SNP_ID_415981409 m1A Human chr9 + 128715393 128715393 128715393 GGCCCCAGGTCCTCCTGGTCCAGTTCAAGGGGACAGGGAAATACTACGCCATCAAAGCACTGAAG GGCCCCAGGTCCTCCTGGTCCAGTTCAAGGGGGCAGGGAAATACTACGCCATCAAAGCACTGAAG A G PKN3 Ensembl:ENSG00000160447 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128715210..128716828 32194978 MeRIP-seq:(Medium) rs779283647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15833,Human_RBP_ID_961635,Human_RBP_ID_3975876,Human_RBP_ID_5633730,Human_RBP_ID_18130403 Human_Splice_Rec_1087702,Human_Splice_Rec_1087703 RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587 107397 RMVar_ID_107397 Human_SNP_ID_415983089 m1A Human chr9 - 128720543 128720543 128720543 TCGAAGTCCCGGAAGGCGGCCTGTTGGCGGGCAGTGAGGAGGCTGTGGGGTGCAGGTGGGGTCAG TCGAAGTCCCGGAAGGCGGCCTGTTGGCGGGCGGTGAGGAGGCTGTGGGGTGCAGGTGGGGTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128720395..128720702 26863196 MeRIP-seq:(Medium) rs767227928 Functional Loss SNV dbSNP153 33..33 33 - - - 107398 RMVar_ID_107398 Human_SNP_ID_415983248 m1A Human chr9 - 128721143 128721142 128721143 CTGGAGGCCGGGCTACCGTCTTGTGCCTGAAAACCACGGGGCCTGTCCCCAGCTGGGGTGAGCGC CTGGAGGCCGGGCTACCGTCTTGTGCCTGAAA_CCACGGGGCCTGTCCCCAGCTGGGGTGAGCGC GT G ZDHHC12 Ensembl:ENSG00000160446 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128721092..128721196 26863196 MeRIP-seq:(Medium) rs746391386 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_712877,Human_RBP_ID_5155034,Human_RBP_ID_17666841,Human_RBP_ID_27370852 107399 RMVar_ID_107399 Human_SNP_ID_415983350 m1A Human chr9 - 128721383 128721383 128721383 CTCGTTGGTGGCCAGCCTGCTCCTCGTCTCGCACCTCTACCTGGTGGCCAGCAACACCACCACCT CTCGTTGGTGGCCAGCCTGCTCCTCGTCTCGCCCCTCTACCTGGTGGCCAGCAACACCACCACCT T G ZDHHC12 Ensembl:ENSG00000160446 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128721334..128721418 26863196 MeRIP-seq:(Medium) rs749333999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17666843,Human_RBP_ID_21658779 Human_Splice_Rec_1087760 107400 RMVar_ID_107400 Human_SNP_ID_415983550 m1A Human chr9 + 128721796 128721796 128721796 GTAGCGGCGGACGCAACGGCGGCACTCACGGCAGTGCCGAGCCCTCAGGGGCTGCTGTGGGCATG GTAGCGGCGGACGCAACGGCGGCACTCACGGCGGTGCCGAGCCCTCAGGGGCTGCTGTGGGCATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128720918..128722579 32194978 MeRIP-seq:(Medium) rs1473363237 Functional Loss SNV dbSNP153 33..33 33 - - - 107401 RMVar_ID_107401 Human_SNP_ID_415996073 m1A Human chr9 - 128770061 128770061 128770061 GAAGAAAGGGAAGAGTGGTTGGCAAGAAAGTCAGAGAACAGTGGGGACCAGAAAAAGGTGGGGAA GAAGAAAGGGAAGAGTGGTTGGCAAGAAAGTCGGAGAACAGTGGGGACCAGAAAAAGGTGGGGAA T C ZER1 Ensembl:ENSG00000160445 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128770053..128770150 26863196 MeRIP-seq:(Medium) rs1024706377 Functional Loss SNV dbSNP153 33..33 33 - - - 107402 RMVar_ID_107402 Human_SNP_ID_415996218 m1A Human chr9 - 128770662 128770662 128770662 TCGCTACTTTGGTTCATTTGTTCATTCAGCAAATAATAAACATGATATGTAAGGAGGTAATAAGT TCGCTACTTTGGTTCATTTGTTCATTCAGCAAGTAATAAACATGATATGTAAGGAGGTAATAAGT T C ZER1 Ensembl:ENSG00000160445 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128770627..128770786 26863196 MeRIP-seq:(Medium) rs1230806039 Functional Loss SNV dbSNP153 33..33 33 - - - 107403 RMVar_ID_107403 Human_SNP_ID_415996464 m1A Human chr9 - 128771750 128771750 128771750 TCCCTCCCGGAGCTCCCGTCCCCGGGATCCCAAGCTCCGCCCCGCCGACCCCCGTCTCCCCTGGA TCCCTCCCGGAGCTCCCGTCCCCGGGATCCCAGGCTCCGCCCCGCCGACCCCCGTCTCCCCTGGA T C ZER1 Ensembl:ENSG00000160445 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128771651..128771850 26863410 MeRIP-seq:(Medium) rs1338542552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5012197,Human_RBP_ID_5243888 Human_miRNA_ID_871652,Human_miRNA_ID_872799 107404 RMVar_ID_107404 Human_SNP_ID_416000975 m1A Human chr9 - 128787362 128787362 128787362 GGCCCCATGGCCCCTTACCGGCTCTTGTGCAGACTTGACATGGTGTTGACTTCCGGACCCCCCAG GGCCCCATGGCCCCTTACCGGCTCTTGTGCAGCCTTGACATGGTGTTGACTTCCGGACCCCCCAG T G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr9:128787271..128788360;chr9:128787333..128787465;chr9:128787227..128788360 26863196 MeRIP-seq:(Medium) rs746321289 Functional Loss SNV dbSNP153 33..33 33 - - - 107405 RMVar_ID_107405 Human_SNP_ID_416003746 m1A Human chr9 - 128798298 128798298 128798298 ACCACGCTCTCTCCCGCTGAGGACTTCGGCATATGCCCTCCTCTCCACCTGGAATGTTCTCTTCT ACCACGCTCTCTCCCGCTGAGGACTTCGGCATGTGCCCTCCTCTCCACCTGGAATGTTCTCTTCT T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128798291..128798439 26863196 MeRIP-seq:(Medium) rs1210229035 Functional Loss SNV dbSNP153 33..33 33 - - - 107406 RMVar_ID_107406 Human_SNP_ID_416009531 m1A Human chr9 - 128818533 128818533 128818533 TCACAAACACTGCCAAGGGCTTGGGCCTCGGAACCCAGAAGGGAGCAGCAGAGCCCAACCGGGTG TCACAAACACTGCCAAGGGCTTGGGCCTCGGAGCCCAGAAGGGAGCAGCAGAGCCCAACCGGGTG T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128818476..128818854 26863196 MeRIP-seq:(Medium) rs999365834 Functional Loss SNV dbSNP153 33..33 33 - - - 107407 RMVar_ID_107407 Human_SNP_ID_416010400 m1A Human chr9 - 128821193 128821154 128821193 GAGAGCTTGGTGCACTGCAGACCTGCGGGGGGAAGGTGGGAGAGCTTGGTGCACTGCAGACCTGC GAGAGCTTGGTGCACTGCAGACCTGCGGGGGG_________________________________ ACCCCCCGCAGGTCTGCAGTGCACCAAGCTCTCCCACCTT A SPOUT1,AL441992.3 Ensembl:ENSG00000198917,Ensembl:ENSG00000286112 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:128821095..128821397 26863196 MeRIP-seq:(Medium) rs1564433253 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_5154717,Human_RBP_ID_5330078,Human_RBP_ID_5535080,Human_RBP_ID_9355062,Human_RBP_ID_18904363,Human_RBP_ID_21995985,Human_RBP_ID_22484579,Human_RBP_ID_26565334,Human_RBP_ID_27542592 107408 RMVar_ID_107408 Human_SNP_ID_416010453 m1A Human chr9 + 128821267 128821267 128821267 CCCTGCAGGTCTGCGGTGCACCAAGCTCTCCCACCTTCCCTCTGCAGGTCCGAGGTGCACCGAGC CCCTGCAGGTCTGCGGTGCACCAAGCTCTCCCCCCTTCCCTCTGCAGGTCCGAGGTGCACCGAGC A C ENDOG Ensembl:ENSG00000167136 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:128821126..128821361 26863196 MeRIP-seq:(Medium) rs559694030 Functional Loss SNV dbSNP153 33..33 33 - - - 107409 RMVar_ID_107409 Human_SNP_ID_416010454 m1A Human chr9 + 128821267 128821267 128821267 CCCTGCAGGTCTGCGGTGCACCAAGCTCTCCCACCTTCCCTCTGCAGGTCCGAGGTGCACCGAGC CCCTGCAGGTCTGCGGTGCACCAAGCTCTCCCGCCTTCCCTCTGCAGGTCCGAGGTGCACCGAGC A G ENDOG Ensembl:ENSG00000167136 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:128821126..128821361 26863196 MeRIP-seq:(Medium) rs559694030 Functional Loss SNV dbSNP153 33..33 33 - - - 107410 RMVar_ID_107410 Human_SNP_ID_416010503 m1A Human chr9 + 128821366 128821366 128821366 CGAGCTCTCACGCCTTCCCCATGCAGGTCCCCAGTGCACCGAGCTCTCCCGCCTTCCCCATGCAG CGAGCTCTCACGCCTTCCCCATGCAGGTCCCCGGTGCACCGAGCTCTCCCGCCTTCCCCATGCAG A G ENDOG Ensembl:ENSG00000167136 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128821276..128821433 26863196 MeRIP-seq:(Medium) rs1490957204 Functional Loss SNV dbSNP153 33..33 33 - - - 107411 RMVar_ID_107411 Human_SNP_ID_416012885 m1A Human chr9 - 128828842 128828842 128828842 GTTCTTTTATCCAGAGAAAGAGGAGAAAAAAAAATGGAAGGATCTCAAGCTGATGAAAAAACTGG GTTCTTTTATCCAGAGAAAGAGGAGAAAAAAAGATGGAAGGATCTCAAGCTGATGAAAAAACTGG T C SPOUT1,AL441992.3 Ensembl:ENSG00000198917,Ensembl:ENSG00000286112 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:128828792..128828915 26863196 MeRIP-seq:(Medium) rs1564436935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407627,Human_RBP_ID_24288124,Human_RBP_ID_26361231,Human_RBP_ID_27832825 Human_Splice_Rec_1087894,Human_Splice_Rec_1087930,Human_Splice_Rec_1087980 107412 RMVar_ID_107412 Human_SNP_ID_416013195 m1A Human chr9 - 128829761 128829761 128829761 GTGTGTGCGGAACATGGCGGAGCGCGGCAGGAAGCGGCCGTGCGGCCCGGTAAGTGCGGGCGGCG GTGTGTGCGGAACATGGCGGAGCGCGGCAGGAGGCGGCCGTGCGGCCCGGTAAGTGCGGGCGGCG T C SPOUT1,AL441992.3 Ensembl:ENSG00000198917,Ensembl:ENSG00000286112 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:128827171..128829800;chr9:128827051..128829825;chr9:128827176..128829825 26863196 MeRIP-seq:(Medium) rs1225477712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256935,Human_RBP_ID_5039372,Human_RBP_ID_26362224 Human_Splice_Rec_1087891,Human_Splice_Rec_1087927,Human_Splice_Rec_1087977 107413 RMVar_ID_107413 Human_SNP_ID_416022292 m1A Human chr9 + 128863977 128863977 128863977 CCCCTTTTCTAGGAAGCAGGCCTTCCCTAGTCAGCTCCTCAACAGCCCTGGCAGTCACCTTTTAT CCCCTTTTCTAGGAAGCAGGCCTTCCCTAGTCGGCTCCTCAACAGCCCTGGCAGTCACCTTTTAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:128863968..128864051 26863196 MeRIP-seq:(Medium) rs915963749 Functional Loss SNV dbSNP153 33..33 33 - - - 107414 RMVar_ID_107414 Human_SNP_ID_416028239 m1A Human chr9 + 128886065 128886065 128886065 GCAAAAGGAATGCCAGGATCCTGCACAGGCAGACGCGGGCCAGCCTCAGCACCGACAGCCGACGC GCAAAAGGAATGCCAGGATCCTGCACAGGCAGGCGCGGGCCAGCCTCAGCACCGACAGCCGACGC A G LRRC8A Ensembl:ENSG00000136802 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128885971..128907205;chr9:128885973..128886169;chr9:128885955..128886125;chr9:128885962..128886125 26863196 MeRIP-seq:(Medium) rs1299186026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961639,Human_RBP_ID_5037508,Human_RBP_ID_19144041 Human_Splice_Rec_1088168,Human_Splice_Rec_1088169,Human_Splice_Rec_1088178,Human_Splice_Rec_1088179,Human_Splice_Rec_1088184 RMVar_hsa_circ_105058,RMVar_hsa_circ_87431,RMVar_hsa_circ_260104,RMVar_hsa_circ_260105 107415 RMVar_ID_107415 Human_SNP_ID_416035996 m1A Human chr9 + 128916323 128916323 128916323 GTGGTGGAGGAGGACCTGTTCAACACACTGCCACCCGAGGTGAAGGAGCGGCTGTGGAGGGCTGA GTGGTGGAGGAGGACCTGTTCAACACACTGCCGCCCGAGGTGAAGGAGCGGCTGTGGAGGGCTGA A G LRRC8A Ensembl:ENSG00000136802 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128916276..128916325 32194978 MeRIP-seq:(Medium) rs750320909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27542645 Human_miRNA_ID_2457236,Human_miRNA_ID_2457237,Human_miRNA_ID_2462158,Human_miRNA_ID_2462159,Human_miRNA_ID_2634802,Human_miRNA_ID_2634803,Human_miRNA_ID_2637489,Human_miRNA_ID_2637490 RMVar_hsa_circ_105058,RMVar_hsa_circ_87431,RMVar_hsa_circ_260104,RMVar_hsa_circ_260105,RMVar_hsa_circ_265466 107416 RMVar_ID_107416 Human_SNP_ID_416044660 m1A Human chr9 - 128947566 128947566 128947566 GATGGCGAGGCCCAAAGAGGTGAGGAGCCGGCAGCGGGGGCGGCTGTAACTGTGAGGAAGGCTGC GATGGCGAGGCCCAAAGAGGTGAGGAGCCGGCGGCGGGGGCGGCTGTAACTGTGAGGAAGGCTGC T C DOLK Ensembl:ENSG00000175283 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128947433..128947572 26863196 MeRIP-seq:(Medium) rs554425491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035924,Human_RBP_ID_22467111 107417 RMVar_ID_107417 Human_SNP_ID_416044661 m1A Human chr9 - 128947566 128947566 128947566 GATGGCGAGGCCCAAAGAGGTGAGGAGCCGGCAGCGGGGGCGGCTGTAACTGTGAGGAAGGCTGC GATGGCGAGGCCCAAAGAGGTGAGGAGCCGGCCGCGGGGGCGGCTGTAACTGTGAGGAAGGCTGC T G DOLK Ensembl:ENSG00000175283 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:128947433..128947572 26863196 MeRIP-seq:(Medium) rs554425491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035924,Human_RBP_ID_22467111 107418 RMVar_ID_107418 Human_SNP_ID_416044791 m1A Human chr9 - 128947744 128947744 128947744 CCGGTCCATTCGACCCGCTCCGCACCTCACACACGGCCCGCCGGCGGCCGCCGCCATCTTCGCGC CCGGTCCATTCGACCCGCTCCGCACCTCACACCCGGCCCGCCGGCGGCCGCCGCCATCTTCGCGC T G RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:128947676..128947865;chr9:128947676..128947900 26863196 MeRIP-seq:(Medium) rs1265978303 Functional Loss SNV dbSNP153 33..33 33 - - - 107419 RMVar_ID_107419 Human_SNP_ID_416044797 m1A Human chr9 + 128947750 128947750 128947750 AGATGGCGGCGGCCGCCGGCGGGCCGTGTGTGAGGTGCGGAGCGGGTCGAATGGACCGGGGTGGC AGATGGCGGCGGCCGCCGGCGGGCCGTGTGTGCGGTGCGGAGCGGGTCGAATGGACCGGGGTGGC A C AL672142.1,NUP188 Ensembl:ENSG00000251184,Ensembl:ENSG00000095319 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr9:128947701..128947843;chr9:128947728..128947815;chr9:128947701..128947845 26863196,26863410,26863196 MeRIP-seq:(Medium) rs767812281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255705,Human_RBP_ID_713008,Human_RBP_ID_847516,Human_RBP_ID_3975889,Human_RBP_ID_5035925,Human_RBP_ID_8930190,Human_RBP_ID_18427228,Human_RBP_ID_19146040 Human_Splice_Rec_1088381,Human_Splice_Rec_1088467 RMVar_hsa_circ_120938,RMVar_hsa_circ_260107 107420 RMVar_ID_107420 Human_SNP_ID_416044920 m1A Human chr9 - 128948016 128948016 128948016 CCAAGAGACGCGTCGGAGGTGAGAGAGGAGGAAGGCAAAGGGCCCTGGGTGAGGAGATGGGAGGC CCAAGAGACGCGTCGGAGGTGAGAGAGGAGGAGGGCAAAGGGCCCTGGGTGAGGAGATGGGAGGC T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128948013..128948078 26863196 MeRIP-seq:(Medium) rs556880461 Functional Loss SNV dbSNP153 33..33 33 - - - 107421 RMVar_ID_107421 Human_SNP_ID_416045331 m1A Human chr9 - 128949212 128949212 128949212 CCAGCTCTCTCAGAGCTGACCTTCCAAGCAGAATAGTCCACAGTTCTCTACTGCTCCTGCAAAAT CCAGCTCTCTCAGAGCTGACCTTCCAAGCAGAGTAGTCCACAGTTCTCTACTGCTCCTGCAAAAT T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:128949176..128949275 26863410 MeRIP-seq:(Medium) rs765872012 Functional Loss SNV dbSNP153 33..33 33 - - - 107422 RMVar_ID_107422 Human_SNP_ID_416046442 m1A Human chr9 - 128952816 128952816 128952816 ACCTGGGAGGTTTGTAGTAAGAAAGCCCCTCTAACAATCGCCGCCAATGTTTATTCAGTTCTGCC ACCTGGGAGGTTTGTAGTAAGAAAGCCCCTCTGACAATCGCCGCCAATGTTTATTCAGTTCTGCC T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128952684..128952850 26863196 MeRIP-seq:(Medium) rs547983716 Functional Loss SNV dbSNP153 33..33 33 - - - 107423 RMVar_ID_107423 Human_SNP_ID_416046444 m1A Human chr9 + 128952819 128952819 128952819 AGAACTGAATAAACATTGGCGGCGATTGTTAGAGGGGCTTTCTTACTACAAACCTCCCAGGTATG AGAACTGAATAAACATTGGCGGCGATTGTTAGGGGGGCTTTCTTACTACAAACCTCCCAGGTATG A G AL672142.1,NUP188 Ensembl:ENSG00000251184,Ensembl:ENSG00000095319 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:128952732..128952850;chr9:128952751..128952850 26863196 MeRIP-seq:(Medium) rs1283413446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3190314,Human_RBP_ID_3974907,Human_RBP_ID_5535088,Human_RBP_ID_8239372,Human_RBP_ID_8944648,Human_RBP_ID_16587904,Human_RBP_ID_24288207 Human_Splice_Rec_1088376,Human_Splice_Rec_1088377,Human_Splice_Rec_1088384,Human_Splice_Rec_1088385,Human_Splice_Rec_1088470,Human_Splice_Rec_1088471,Human_Splice_Rec_1088480,Human_Splice_Rec_1088481,Human_Splice_Rec_1088486 RMVar_hsa_circ_24403,RMVar_hsa_circ_97917,RMVar_hsa_circ_120938,RMVar_hsa_circ_316809,RMVar_hsa_circ_260107,RMVar_hsa_circ_116606,RMVar_hsa_circ_47127,RMVar_hsa_circ_87111,RMVar_hsa_circ_31758,RMVar_hsa_circ_34807,RMVar_hsa_circ_260109,RMVar_hsa_circ_14541,RMVar_hsa_circ_260110,RMVar_hsa_circ_328189,RMVar_hsa_circ_260108,RMVar_hsa_circ_264929,RMVar_hsa_circ_260111 107424 RMVar_ID_107424 Human_SNP_ID_416059991 m1A Human chr9 + 129001645 129001645 129001645 CTCCCCATCCTACCCACCCTCCTCACCACTCTAGAGGTGAGCCTTCGCATGAAGCAGAACCTGCA CTCCCCATCCTACCCACCCTCCTCACCACTCTGGAGGTGAGCCTTCGCATGAAGCAGAACCTGCA A G NUP188 Ensembl:ENSG00000095319 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128999242..129001749 32194978 MeRIP-seq:(Medium) rs762411426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27542714 Human_Splice_Rec_1088449,Human_Splice_Rec_1088519 Human_miRNA_ID_2797664,Human_miRNA_ID_2798630,Human_miRNA_ID_2800011,Human_miRNA_ID_2807326,Human_miRNA_ID_2810470,Human_miRNA_ID_2813612,Human_miRNA_ID_2833202,Human_miRNA_ID_2852725,Human_miRNA_ID_2853787,Human_miRNA_ID_2860869 RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_260172,RMVar_hsa_circ_98396,RMVar_hsa_circ_113549,RMVar_hsa_circ_260184,RMVar_hsa_circ_260185,RMVar_hsa_circ_96102,RMVar_hsa_circ_260188,RMVar_hsa_circ_113038,RMVar_hsa_circ_96283,RMVar_hsa_circ_260191,RMVar_hsa_circ_260192,RMVar_hsa_circ_260193,RMVar_hsa_circ_375587 107425 RMVar_ID_107425 Human_SNP_ID_416061521 m1A Human chr9 + 129006122 129006122 129006122 TCAGCACACAGGCAGAAGGGACCAGGACGTTAAAGTAAGTGCTCTTTCTGGGATTTGATAAGGGG TCAGCACACAGGCAGAAGGGACCAGGACGTTACAGTAAGTGCTCTTTCTGGGATTTGATAAGGGG A C NUP188 Ensembl:ENSG00000095319 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129006098..129006946 32194978 MeRIP-seq:(Medium) rs1207009313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19144054,Human_RBP_ID_26239892 Human_Splice_Rec_1088462,Human_Splice_Rec_1088463 RMVar_hsa_circ_125507,RMVar_hsa_circ_260124,RMVar_hsa_circ_108464,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_20473,RMVar_hsa_circ_260145,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_119813,RMVar_hsa_circ_260172,RMVar_hsa_circ_98396,RMVar_hsa_circ_260192,RMVar_hsa_circ_93220,RMVar_hsa_circ_260194 107426 RMVar_ID_107426 Human_SNP_ID_416061720 m1A Human chr9 + 129006550 129006550 129006550 GCCTCTCGCGCTACTTCCGCCGGGGAGCCCCCAGCTCCCCTGCCACTGGTGTCCTCCCCTCGCCG GCCTCTCGCGCTACTTCCGCCGGGGAGCCCCCCGCTCCCCTGCCACTGGTGTCCTCCCCTCGCCG A C NUP188 Ensembl:ENSG00000095319 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129006526..129006550 26863196 MeRIP-seq:(Medium) rs745531014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713038,Human_RBP_ID_18173279 Human_Splice_Rec_1088466 RMVar_hsa_circ_125507,RMVar_hsa_circ_260124,RMVar_hsa_circ_84257,RMVar_hsa_circ_260144,RMVar_hsa_circ_119813,RMVar_hsa_circ_260172,RMVar_hsa_circ_93220,RMVar_hsa_circ_260194,RMVar_hsa_circ_260195,RMVar_hsa_circ_103636 107427 RMVar_ID_107427 Human_SNP_ID_416061721 m1A Human chr9 + 129006550 129006550 129006550 GCCTCTCGCGCTACTTCCGCCGGGGAGCCCCCAGCTCCCCTGCCACTGGTGTCCTCCCCTCGCCG GCCTCTCGCGCTACTTCCGCCGGGGAGCCCCCGGCTCCCCTGCCACTGGTGTCCTCCCCTCGCCG A G NUP188 Ensembl:ENSG00000095319 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129006526..129006550 26863196 MeRIP-seq:(Medium) rs745531014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713038,Human_RBP_ID_18173279 Human_Splice_Rec_1088466 RMVar_hsa_circ_125507,RMVar_hsa_circ_260124,RMVar_hsa_circ_84257,RMVar_hsa_circ_260144,RMVar_hsa_circ_119813,RMVar_hsa_circ_260172,RMVar_hsa_circ_93220,RMVar_hsa_circ_260194,RMVar_hsa_circ_260195,RMVar_hsa_circ_103636 107428 RMVar_ID_107428 Human_SNP_ID_416062265 m1A Human chr9 - 129008136 129008136 129008136 CCCTCCCACCCCTCACAGCTCAAGCCAAGTCCAGCGGCCGCAGTCTTCACCTCTCCACACTCACT CCCTCCCACCCCTCACAGCTCAAGCCAAGTCCTGCGGCCGCAGTCTTCACCTCTCCACACTCACT T A SH3GLB2 Ensembl:ENSG00000148341 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129008086..129008196 26863196 MeRIP-seq:(Medium) rs1189072419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27542718 Human_miRNA_ID_131382,Human_miRNA_ID_174721,Human_miRNA_ID_1149490,Human_miRNA_ID_1229647,Human_miRNA_ID_2541809,Human_miRNA_ID_2543685,Human_miRNA_ID_2545536,Human_miRNA_ID_2547390,Human_miRNA_ID_2549254,Human_miRNA_ID_2551123,Human_miRNA_ID_2556528,Human_miRNA_ID_2558410,Human_miRNA_ID_2588829 RMVar_hsa_circ_82846,RMVar_hsa_circ_97590,RMVar_hsa_circ_122344,RMVar_hsa_circ_113635,RMVar_hsa_circ_90203,RMVar_hsa_circ_94975,RMVar_hsa_circ_85853,RMVar_hsa_circ_260197,RMVar_hsa_circ_260199,RMVar_hsa_circ_260201,RMVar_hsa_circ_260202,RMVar_hsa_circ_260203,RMVar_hsa_circ_260200,RMVar_hsa_circ_260198 107429 RMVar_ID_107429 Human_SNP_ID_416062268 m1A Human chr9 - 129008152 129008152 129008152 TTCCGGTGCTATCCTCCCCTCCCACCCCTCACAGCTCAAGCCAAGTCCAGCGGCCGCAGTCTTCA TTCCGGTGCTATCCTCCCCTCCCACCCCTCACGGCTCAAGCCAAGTCCAGCGGCCGCAGTCTTCA T C SH3GLB2 Ensembl:ENSG00000148341 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129008102..129008241 26863196 MeRIP-seq:(Medium) rs1244046433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22336103 Human_miRNA_ID_2541809,Human_miRNA_ID_2543685,Human_miRNA_ID_2545536,Human_miRNA_ID_2547390,Human_miRNA_ID_2549254,Human_miRNA_ID_2551123,Human_miRNA_ID_2556528,Human_miRNA_ID_2558410,Human_miRNA_ID_2588829,Human_miRNA_ID_2672584 RMVar_hsa_circ_82846,RMVar_hsa_circ_97590,RMVar_hsa_circ_122344,RMVar_hsa_circ_113635,RMVar_hsa_circ_90203,RMVar_hsa_circ_94975,RMVar_hsa_circ_85853,RMVar_hsa_circ_260197,RMVar_hsa_circ_260199,RMVar_hsa_circ_260201,RMVar_hsa_circ_260202,RMVar_hsa_circ_260203,RMVar_hsa_circ_260200,RMVar_hsa_circ_260198 107430 RMVar_ID_107430 Human_SNP_ID_416063079 m1A Human chr9 + 129010221 129010221 129010221 CACGCGGAGCTCCTGCTCGGCCTGGGCAGGGCAGGGCAGCCATGAGCACCCACACACCACCCACC CACGCGGAGCTCCTGCTCGGCCTGGGCAGGGCGGGGCAGCCATGAGCACCCACACACCACCCACC A G NONHSAG053566.2,NONHSAG053566.2:2 RNACentral:URS00009C4881,RNACentral:URS00008B3B47 lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129010218..129010343 26863196 MeRIP-seq:(Medium) rs13440035 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 107431 RMVar_ID_107431 Human_SNP_ID_416063173 m1A Human chr9 - 129010633 129010633 129010633 GTTGGGGCCTGGGGGGCTGGGCTCGAGGAAGAAGGGGTGGCGGGGTGCAGGCACACTTGCTGCTG GTTGGGGCCTGGGGGGCTGGGCTCGAGGAAGACGGGGTGGCGGGGTGCAGGCACACTTGCTGCTG T G SH3GLB2 Ensembl:ENSG00000148341 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129010631..129010766 26863196 MeRIP-seq:(Medium) rs1340126180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847254,Human_RBP_ID_3974926,Human_RBP_ID_5407462,Human_RBP_ID_9442043,Human_RBP_ID_19144057,Human_RBP_ID_22426736,Human_RBP_ID_26361236 Human_Splice_Rec_1088560,Human_Splice_Rec_1088590,Human_Splice_Rec_1088612,Human_Splice_Rec_1088640,Human_Splice_Rec_1088660,Human_Splice_Rec_1088676,Human_Splice_Rec_1088694 RMVar_hsa_circ_82846,RMVar_hsa_circ_113635,RMVar_hsa_circ_90203,RMVar_hsa_circ_94975,RMVar_hsa_circ_260197,RMVar_hsa_circ_260199,RMVar_hsa_circ_260200,RMVar_hsa_circ_260198 107432 RMVar_ID_107432 Human_SNP_ID_416063595 m1A Human chr9 + 129011996 129011996 129011996 CCACACTACTCAGTGTGGCTGGCCCTGCCGCCAGCTCCAGCGTTTTGCAGAGGGAAACAAGTCCA CCACACTACTCAGTGTGGCTGGCCCTGCCGCCCGCTCCAGCGTTTTGCAGAGGGAAACAAGTCCA A C NONHSAG053566.2 RNACentral:URS00009C4881 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129011994..129012130 26863196 MeRIP-seq:(Medium) rs902190633 Functional Loss SNV dbSNP153 33..33 33 - - - 107433 RMVar_ID_107433 Human_SNP_ID_416066338 m1A Human chr9 + 129021147 129021147 129021147 CACTGGCCGCGTCTGCCATGTACTGAGCCAGCAGCTCCCCGTTGGTGACCCTTGAGGGGACCTTC CACTGGCCGCGTCTGCCATGTACTGAGCCAGCGGCTCCCCGTTGGTGACCCTTGAGGGGACCTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129021076..129021261 26863196 MeRIP-seq:(Medium) rs773547098 Functional Loss SNV dbSNP153 33..33 33 - - - 107434 RMVar_ID_107434 Human_SNP_ID_416066705 m1A Human chr9 - 129022420 129022420 129022420 CCCACCCCTTGGCCTTCCCCTCTGCGTAGTTCACGGAGGAGAAATTTGGCCAGGCTGAGAAGACT CCCACCCCTTGGCCTTCCCCTCTGCGTAGTTCGCGGAGGAGAAATTTGGCCAGGCTGAGAAGACT T C SH3GLB2 Ensembl:ENSG00000148341 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129022233..129022481 26863196 MeRIP-seq:(Medium) rs780911505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5039478,Human_RBP_ID_18904453,Human_RBP_ID_19025821 Human_Splice_Rec_1088550,Human_Splice_Rec_1088580,Human_Splice_Rec_1088600,Human_Splice_Rec_1088630,Human_Splice_Rec_1088652,Human_Splice_Rec_1088684,Human_Splice_Rec_1088710 RMVar_hsa_circ_82846,RMVar_hsa_circ_260197,RMVar_hsa_circ_373500,RMVar_hsa_circ_260205 107435 RMVar_ID_107435 Human_SNP_ID_416068232 m1A Human chr9 + 129028153 129028153 129028153 CGTCCGACGCCAGCTTCTTCATGTTGAAGTCCATGGCGTGCCCGCACGGCCGCCGCGCACGGCCC CGTCCGACGCCAGCTTCTTCATGTTGAAGTCCCTGGCGTGCCCGCACGGCCGCCGCGCACGGCCC A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129028076..129028339 26863196 MeRIP-seq:(Medium) rs750116212 Functional Loss SNV dbSNP153 33..33 33 - - - 107436 RMVar_ID_107436 Human_SNP_ID_416068321 m1A Human chr9 - 129028291 129028291 129028291 TCGGGCTGGCTCGGCGGCTGCGGCGGGCGGGCAGGCGGGCAGGCCGGCAGGCGGGTGCGCGGAGG TCGGGCTGGCTCGGCGGCTGCGGCGGGCGGGCGGGCGGGCAGGCCGGCAGGCGGGTGCGCGGAGG T C SH3GLB2 Ensembl:ENSG00000148341 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:129028190..129028303 26863410 MeRIP-seq:(Medium) rs1268137285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256122,Human_RBP_ID_9339108,Human_RBP_ID_18427231 RMVar_hsa_circ_82846,RMVar_hsa_circ_260197 107437 RMVar_ID_107437 Human_SNP_ID_416070926 m1A Human chr9 + 129037174 129037174 129037174 CCCGGCATGGTGGGACTATTGAGGGGTCCGGCATGGGGTGAATAGGAGACTGGGCAGAGTGGCTC CCCGGCATGGTGGGACTATTGAGGGGTCCGGCGTGGGGTGAATAGGAGACTGGGCAGAGTGGCTC A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129037146..129037260 26863196 MeRIP-seq:(Medium) rs888745272 Functional Loss SNV dbSNP153 33..33 33 - - - 107438 RMVar_ID_107438 Human_SNP_ID_416074440 m1A Human chr9 + 129049954 129049954 129049954 GGCCTCCGGAACCCAGAGACTGCATCAGAGCCACTGTCTGAGGTAGGTGGTCTTCTGCATCCCCC GGCCTCCGGAACCCAGAGACTGCATCAGAGCCGCTGTCTGAGGTAGGTGGTCTTCTGCATCCCCC A G MIGA2 Ensembl:ENSG00000148343 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:129049897..129050009 26863410 MeRIP-seq:(Medium) rs776832672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961656,Human_RBP_ID_27832836 Human_Splice_Rec_1088739,Human_Splice_Rec_1088771,Human_Splice_Rec_1088797 RMVar_hsa_circ_23543,RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_276229,RMVar_hsa_circ_260206,RMVar_hsa_circ_260208 107439 RMVar_ID_107439 Human_SNP_ID_416080544 m1A Human chr9 + 129071222 129071222 129071222 TGGTGCTAGGCTCTGAGCTGGGGGCTCAGACCAGGGATCGCTCAGGCCCCTGTCACCTGTGGGCC TGGTGCTAGGCTCTGAGCTGGGGGCTCAGACCCGGGATCGCTCAGGCCCCTGTCACCTGTGGGCC A C MIGA2 Ensembl:ENSG00000148343 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129071171..129071292 26863196 MeRIP-seq:(Medium) rs952996868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798306,Human_RBP_ID_22628543 Human_miRNA_ID_445923 107440 RMVar_ID_107440 Human_SNP_ID_416088476 m1A Human chr9 - 129099952 129099952 129099952 CTCCCTTCCCTTCCACAGTTCATCGTGGCAGAAGATGGCTCCTGTGGGCTTGTGTACGAGCATGC CTCCCTTCCCTTCCACAGTTCATCGTGGCAGATGATGGCTCCTGTGGGCTTGTGTACGAGCATGC T A CRAT Ensembl:ENSG00000095321 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129099901..129099975 32194978 MeRIP-seq:(Medium) rs1167178522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19025838 Human_Splice_Rec_1088918,Human_Splice_Rec_1088919,Human_Splice_Rec_1088954,Human_Splice_Rec_1088955 RMVar_hsa_circ_90666,RMVar_hsa_circ_125599,RMVar_hsa_circ_98320,RMVar_hsa_circ_80075,RMVar_hsa_circ_3873,RMVar_hsa_circ_260215,RMVar_hsa_circ_260217,RMVar_hsa_circ_260218,RMVar_hsa_circ_260216,RMVar_hsa_circ_260219,RMVar_hsa_circ_93494,RMVar_hsa_circ_96409,RMVar_hsa_circ_260223,RMVar_hsa_circ_66136 107441 RMVar_ID_107441 Human_SNP_ID_416090836 m1A Human chr9 - 129107911 129107911 129107911 GCAGCCCATCGTGAGTGAGGAGGAGTGGGCCCACACCAAGCAGCTGGTGGATGAGTTTCAGGCCT GCAGCCCATCGTGAGTGAGGAGGAGTGGGCCCTCACCAAGCAGCTGGTGGATGAGTTTCAGGCCT T A CRAT Ensembl:ENSG00000095321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129107863..129107946 26863196 MeRIP-seq:(Medium) rs756737105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184234 Human_Splice_Rec_1088907,Human_Splice_Rec_1088943,Human_Splice_Rec_1088975,Human_Splice_Rec_1088985,Human_Splice_Rec_1088997 RMVar_hsa_circ_90666,RMVar_hsa_circ_260218,RMVar_hsa_circ_96409,RMVar_hsa_circ_260223,RMVar_hsa_circ_118987,RMVar_hsa_circ_260226 107442 RMVar_ID_107442 Human_SNP_ID_416090837 m1A Human chr9 - 129107911 129107911 129107911 GCAGCCCATCGTGAGTGAGGAGGAGTGGGCCCACACCAAGCAGCTGGTGGATGAGTTTCAGGCCT GCAGCCCATCGTGAGTGAGGAGGAGTGGGCCCGCACCAAGCAGCTGGTGGATGAGTTTCAGGCCT T C CRAT Ensembl:ENSG00000095321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129107863..129107946 26863196 MeRIP-seq:(Medium) rs756737105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184234 Human_Splice_Rec_1088907,Human_Splice_Rec_1088943,Human_Splice_Rec_1088975,Human_Splice_Rec_1088985,Human_Splice_Rec_1088997 RMVar_hsa_circ_90666,RMVar_hsa_circ_260218,RMVar_hsa_circ_96409,RMVar_hsa_circ_260223,RMVar_hsa_circ_118987,RMVar_hsa_circ_260226 107443 RMVar_ID_107443 Human_SNP_ID_416091586 m1A Human chr9 + 129110632 129110632 129110632 TCCTTGCTAGAGCCTTCGGGCCAAGGTCGCTGAGTTACAGCCGCCAGCCGGTAGAGGCAGCCCCG TCCTTGCTAGAGCCTTCGGGCCAAGGTCGCTGGGTTACAGCCGCCAGCCGGTAGAGGCAGCCCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129110581..129110762 26863196 MeRIP-seq:(Medium) rs1043012334 Functional Loss SNV dbSNP153 33..33 33 - - - 107444 RMVar_ID_107444 Human_SNP_ID_416091599 m1A Human chr9 - 129110676 129110676 129110676 CCCCGGGTGCCTTCCCGCAGCCCGCTCGGCCCAGAGGGTGGGCGCGGGGCTGCCTCTACCGGCTG CCCCGGGTGCCTTCCCGCAGCCCGCTCGGCCCGGAGGGTGGGCGCGGGGCTGCCTCTACCGGCTG T C CRAT Ensembl:ENSG00000095321 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129110628..129110735 26863196 MeRIP-seq:(Medium) rs1302246733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035928 107445 RMVar_ID_107445 Human_SNP_ID_416091609 m1A Human chr9 + 129110696 129110696 129110696 GCGCCCACCCTCTGGGCCGAGCGGGCTGCGGGAAGGCACCCGGGGAGGAGGACTCGCGAGGCGGG GCGCCCACCCTCTGGGCCGAGCGGGCTGCGGGCAGGCACCCGGGGAGGAGGACTCGCGAGGCGGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:129110601..129110775 26863410 MeRIP-seq:(Medium) rs3118624 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14738 107446 RMVar_ID_107446 Human_SNP_ID_416091988 m1A Human chr9 + 129111559 129111559 129111559 GAGGAAGGGTGGGTGCAAGAGTGAAAGGCGAGAGGGGACTGCAAGCATCCGGGTCGGCTCCTGGC GAGGAAGGGTGGGTGCAAGAGTGAAAGGCGAGTGGGGACTGCAAGCATCCGGGTCGGCTCCTGGC A T PTPA Ensembl:ENSG00000119383 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:129111362..129111625;chr9:129111412..129111680 26863196 MeRIP-seq:(Medium) rs1431657368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847524,Human_RBP_ID_5037516,Human_RBP_ID_5633753,Human_RBP_ID_22467117 Human_Splice_Rec_1089008,Human_Splice_Rec_1089009,Human_Splice_Rec_1089028,Human_Splice_Rec_1089029,Human_Splice_Rec_1089043,Human_Splice_Rec_1089059,Human_Splice_Rec_1089079,Human_Splice_Rec_1089097,Human_Splice_Rec_1089115,Human_Splice_Rec_1089121,Human_Splice_Rec_1089135,Human_Splice_Rec_1089151 RMVar_hsa_circ_93454,RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260228,RMVar_hsa_circ_44760 107447 RMVar_ID_107447 Human_SNP_ID_416096700 m1A Human chr9 - 129129010 129129010 129129010 GAGTCTCATCAATCCACCTGTCCAGCGTGTTGAGAAGAGCGACTAGTTTCTCAATGGCCTGTGGA GAGTCTCATCAATCCACCTGTCCAGCGTGTTGCGAAGAGCGACTAGTTTCTCAATGGCCTGTGGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:129128985..129129086 32194978 MeRIP-seq:(Medium) rs1392241028 Functional Loss SNV dbSNP153 33..33 33 - - - 107448 RMVar_ID_107448 Human_SNP_ID_416099516 m1A Human chr9 + 129139430 129139430 129139430 GAGGGCGTGCCTAGAGTTGTTGGCTGTTCCGCACCTTCTCCACAGGTCCGGGTTTTCACTTTGGG GAGGGCGTGCCTAGAGTTGTTGGCTGTTCCGCGCCTTCTCCACAGGTCCGGGTTTTCACTTTGGG A G PTPA Ensembl:ENSG00000119383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129139427..129139583 26863196 MeRIP-seq:(Medium) rs1394329871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_260231,RMVar_hsa_circ_292472,RMVar_hsa_circ_123544,RMVar_hsa_circ_260232,RMVar_hsa_circ_37047,RMVar_hsa_circ_334371,RMVar_hsa_circ_260235,RMVar_hsa_circ_374996 107449 RMVar_ID_107449 Human_SNP_ID_416100013 m1A Human chr9 + 129140867 129140867 129140867 GGTTGAGCAGGGCAGTTGAAACAAAGCTCCCCAGAGGTGAGGCCCCTGTAGGCTCGGGGTGCCTG GGTTGAGCAGGGCAGTTGAAACAAAGCTCCCCGGAGGTGAGGCCCCTGTAGGCTCGGGGTGCCTG A G PTPA Ensembl:ENSG00000119383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129140862..129141047 26863196 MeRIP-seq:(Medium) rs1452546284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3908815,Human_RBP_ID_5329651,Human_RBP_ID_9442045 RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_260231,RMVar_hsa_circ_292472,RMVar_hsa_circ_123544,RMVar_hsa_circ_260232,RMVar_hsa_circ_37047,RMVar_hsa_circ_334371,RMVar_hsa_circ_260235,RMVar_hsa_circ_374996 107450 RMVar_ID_107450 Human_SNP_ID_416100052 m1A Human chr9 + 129140972 129140972 129140972 GAAGCGAGTGGTCCAAGACAAGGCCCCCAGGGACCAGAGTGGGCTTTGTCTCTGTTGGGTGCCTC GAAGCGAGTGGTCCAAGACAAGGCCCCCAGGGCCCAGAGTGGGCTTTGTCTCTGTTGGGTGCCTC A C PTPA Ensembl:ENSG00000119383 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129140969..129141079 26863196 MeRIP-seq:(Medium) rs942715111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_260231,RMVar_hsa_circ_292472,RMVar_hsa_circ_123544,RMVar_hsa_circ_260232,RMVar_hsa_circ_37047,RMVar_hsa_circ_334371,RMVar_hsa_circ_260235,RMVar_hsa_circ_374996 107451 RMVar_ID_107451 Human_SNP_ID_416100654 m1A Human chr9 + 129142407 129142407 129142407 TGCTGCAGGGGAGGAGGGATGAGCTCCCAGCCAGAACCTGTCTCTTCAGCTTGTGGCTTCTCTTT TGCTGCAGGGGAGGAGGGATGAGCTCCCAGCCGGAACCTGTCTCTTCAGCTTGTGGCTTCTCTTT A G PTPA Ensembl:ENSG00000119383 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129142403..129142592 26863196 MeRIP-seq:(Medium) rs1564202510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962305,Human_RBP_ID_5658634,Human_RBP_ID_24288396 RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_260231,RMVar_hsa_circ_292472,RMVar_hsa_circ_123544,RMVar_hsa_circ_260232,RMVar_hsa_circ_37047,RMVar_hsa_circ_334371,RMVar_hsa_circ_260235,RMVar_hsa_circ_374996 107452 RMVar_ID_107452 Human_SNP_ID_416102484 m1A Human chr9 + 129147394 129147394 129147394 CTGCTCACCTGCTCCTTCCTCACAGTGCCTGGAGAAGTTCCCTGTGATCCAGCACTTCAAGTTCG CTGCTCACCTGCTCCTTCCTCACAGTGCCTGGGGAAGTTCCCTGTGATCCAGCACTTCAAGTTCG A G PTPA Ensembl:ENSG00000119383 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129147385..129147901 26863196 MeRIP-seq:(Medium) rs767774479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5454205 Human_Splice_Rec_1089026,Human_Splice_Rec_1089058,Human_Splice_Rec_1089078,Human_Splice_Rec_1089096,Human_Splice_Rec_1089114,Human_Splice_Rec_1089120,Human_Splice_Rec_1089150,Human_Splice_Rec_1089194,Human_Splice_Rec_1089228,Human_Splice_Rec_1089236,Human_Splice_Rec_1089246,Human_Splice_Rec_1089250,Human_Splice_Rec_1089254,Human_Splice_Rec_1089258 Human_miRNA_ID_2000074,Human_miRNA_ID_2000075,Human_miRNA_ID_2777433,Human_miRNA_ID_2777434 RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_115240,RMVar_hsa_circ_260231,RMVar_hsa_circ_123544,RMVar_hsa_circ_109248,RMVar_hsa_circ_260237 107453 RMVar_ID_107453 Human_SNP_ID_416102535 m1A Human chr9 - 129147500 129147500 129147500 GCCACTGCTGGGGTGGGGAAGGCAGGCACAGGAACTGTGGCCTGGGTGGCTCTTCGGCTTGGCCC GCCACTGCTGGGGTGGGGAAGGCAGGCACAGGTACTGTGGCCTGGGTGGCTCTTCGGCTTGGCCC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129147451..129147901 32194978 MeRIP-seq:(Medium) rs1381103435 Functional Loss SNV dbSNP153 33..33 33 - - - 107454 RMVar_ID_107454 Human_SNP_ID_416102827 m1A Human chr9 - 129148388 129148388 129148388 AGGGCCCAGGGGCCCAGGGTGAGGCTCACAGCAGCGCAAAGGTAGCAGAAGTGGCCGGGCCTAAG AGGGCCCAGGGGCCCAGGGTGAGGCTCACAGCGGCGCAAAGGTAGCAGAAGTGGCCGGGCCTAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:129148133..129148540;chr9:129148230..129148531 26863196 MeRIP-seq:(Medium) rs1306173146 Functional Loss SNV dbSNP153 33..33 33 - - - 107455 RMVar_ID_107455 Human_SNP_ID_416110710 m1A Human chr9 - 129176739 129176727 129176739 GGCGAGAGGAGGGAACGAGCGGGCGCCGGGCCACTCGGGGCTGAGCTGGGGGCGAGCGGGGGCAG GGCGAGAGGAGGGAACGAGCGGGCGCCGGGCC____________GCTGGGGGCGAGCGGGGGCAG CTCAGCCCCGAGT C IER5L Ensembl:ENSG00000188483 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129176534..129177600 26863196 MeRIP-seq:(Medium) rs1448895769 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_798798,Human_RBP_ID_5410164,Human_RBP_ID_22119903,Human_RBP_ID_24555440,Human_RBP_ID_27542768 Human_miRNA_ID_941229 107456 RMVar_ID_107456 Human_SNP_ID_416110712 m1A Human chr9 - 129176739 129176739 129176739 GGCGAGAGGAGGGAACGAGCGGGCGCCGGGCCACTCGGGGCTGAGCTGGGGGCGAGCGGGGGCAG GGCGAGAGGAGGGAACGAGCGGGCGCCGGGCCTCTCGGGGCTGAGCTGGGGGCGAGCGGGGGCAG T A IER5L Ensembl:ENSG00000188483 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129176534..129177600 26863196 MeRIP-seq:(Medium) rs1157160171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_798798,Human_RBP_ID_5410164,Human_RBP_ID_22119903,Human_RBP_ID_24555440,Human_RBP_ID_27542768 Human_miRNA_ID_941229 107457 RMVar_ID_107457 Human_SNP_ID_416110778 m1A Human chr9 - 129176856 129176856 129176856 CAGGCGCTCGCCAGCCTCGGCGCCTGGACTCGAGCCATTGTCGCCTTCTAGGGACCCCCGAGGGC CAGGCGCTCGCCAGCCTCGGCGCCTGGACTCGCGCCATTGTCGCCTTCTAGGGACCCCCGAGGGC T G IER5L Ensembl:ENSG00000188483 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:129176783..129177129 32194978 MeRIP-seq:(Medium) rs1049003806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27542772 107458 RMVar_ID_107458 Human_SNP_ID_416111139 m1A Human chr9 + 129177487 129177487 129177487 GCGGGCAGAGCGCAGCGGGCGCGGGCGGCGGCAGCGGCAGCGGCAGCGGCGCAGGACCCGGCTGC GCGGGCAGAGCGCAGCGGGCGCGGGCGGCGGCGGCGGCAGCGGCAGCGGCGCAGGACCCGGCTGC A G AL158151.3,AL158151.1 Ensembl:ENSG00000268050,Ensembl:ENSG00000204055 lincRNA,lincRNA exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129177325..129177600 26863196 MeRIP-seq:(Medium) rs991492171 Functional Loss SNV dbSNP153 33..33 33 - - - 107459 RMVar_ID_107459 Human_SNP_ID_416111326 m1A Human chr9 + 129177824 129177824 129177824 GGCCGCGCTGGCCGGCATGCCCGGCGCCGCGTACGCTAGGTGCTGGTGCTGGTGGTGGGGCGGCT GGCCGCGCTGGCCGGCATGCCCGGCGCCGCGTCCGCTAGGTGCTGGTGCTGGTGGTGGGGCGGCT A C AL158151.1 Ensembl:ENSG00000204055 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129177776..129177825 26863196 MeRIP-seq:(Medium) rs1163646620 Functional Loss SNV dbSNP153 33..33 33 - - - 107460 RMVar_ID_107460 Human_SNP_ID_416111351 m1A Human chr9 - 129177874 129177874 129177874 CGAGCGCTACGCCGAGCTCTACCGGCGCCAGCAGCAGCAGCAACAGCAGCAGCCGCCCCACCACC CGAGCGCTACGCCGAGCTCTACCGGCGCCAGCTGCAGCAGCAACAGCAGCAGCCGCCCCACCACC T A IER5L Ensembl:ENSG00000188483 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:129177826..129177900 26863196 MeRIP-seq:(Medium) rs1196598068 Functional Loss SNV dbSNP153 33..33 33 - - - 107461 RMVar_ID_107461 Human_SNP_ID_416111374 m1A Human chr9 + 129177916 129177916 129177916 GGTAGAGCTCGGCGTAGCGCTCGCTCAGGTAGAGCTGGCGCGCGTTGCGGAGCACGTAGGACACC GGTAGAGCTCGGCGTAGCGCTCGCTCAGGTAGCGCTGGCGCGCGTTGCGGAGCACGTAGGACACC A C AL158151.1 Ensembl:ENSG00000204055 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:129177867..129178065 32194978 MeRIP-seq:(Medium) rs760051741 Functional Loss SNV dbSNP153 33..33 33 - - - 107462 RMVar_ID_107462 Human_SNP_ID_416111390 m1A Human chr9 - 129177958 129177958 129177958 CCGAACCCAGCGCGGCGGCATCAAGCTGCACAAGAACCTCCTGGTGTCCTACGTGCTCCGCAACG CCGAACCCAGCGCGGCGGCATCAAGCTGCACAGGAACCTCCTGGTGTCCTACGTGCTCCGCAACG T C IER5L Ensembl:ENSG00000188483 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129176820..129201346 32194978 MeRIP-seq:(Medium) rs749998469 Functional Loss SNV dbSNP153 33..33 33 - - - 107463 RMVar_ID_107463 Human_SNP_ID_416111501 m1A Human chr9 - 129178206 129178206 129178206 GGGAGCGCGAGCCCGCGGGTGGCGCGCGGCGCATGGTGGCGGCTCCTTTCGGAGCGCAGCCGAAC GGGAGCGCGAGCCCGCGGGTGGCGCGCGGCGCTTGGTGGCGGCTCCTTTCGGAGCGCAGCCGAAC T A IER5L Ensembl:ENSG00000188483 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr9:129177916..129178250;chr9:129178113..129178225 26863196,26863410 MeRIP-seq:(Medium) rs1053368127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037178 107464 RMVar_ID_107464 Human_SNP_ID_416111502 m1A Human chr9 - 129178206 129178206 129178206 GGGAGCGCGAGCCCGCGGGTGGCGCGCGGCGCATGGTGGCGGCTCCTTTCGGAGCGCAGCCGAAC GGGAGCGCGAGCCCGCGGGTGGCGCGCGGCGCGTGGTGGCGGCTCCTTTCGGAGCGCAGCCGAAC T C IER5L Ensembl:ENSG00000188483 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr9:129177916..129178250;chr9:129178113..129178225 26863196,26863410 MeRIP-seq:(Medium) rs1053368127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5037178 107465 RMVar_ID_107465 Human_SNP_ID_416152729 m1A Human chr9 - 129333958 129333958 129333958 CGACACTTAGGGAACCCTGTGAGAGCAGAGGGAGAGAGTTCCAGGCAGAGGAGGCAGCAAGTGTG CGACACTTAGGGAACCCTGTGAGAGCAGAGGGGGAGAGTTCCAGGCAGAGGAGGCAGCAAGTGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129333908..129334104 26863196 MeRIP-seq:(Medium) rs999627824 Functional Loss SNV dbSNP153 33..33 33 - - - 107466 RMVar_ID_107466 Human_SNP_ID_416154555 m1A Human chr9 - 129340199 129340184 129340200 CATACACACCAACTCACACATCTCACATACACACCAACTCACACGCATACCAACTCACACATACA CATACACACCAACTCACACATCTCACATACA________________TACCAACTCACACATACA ATGCGTGTGAGTTGGTG A lnc-IER5L-1,lnc-IER5L-1:2 RNACentral:URS00008BE9C6,RNACentral:URS00008B75A0 lincRNA,lincRNA exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr9:129339675..129340448;chr9:129340114..129340343 26863196 MeRIP-seq:(Medium) rs1259464514 Functional Loss DEL dbSNP153 32..47 33 - - - 107467 RMVar_ID_107467 Human_SNP_ID_416154582 m1A Human chr9 + 129340234 129340234 129340234 GTATGTGAGATGTGTGAGTTGGTGTGTATGCGAGTTGATGTGAGTTGTGTATGTGTGAGTTGGTG GTATGTGAGATGTGTGAGTTGGTGTGTATGCGTGTTGATGTGAGTTGTGTATGTGTGAGTTGGTG A T LINC01503 Ensembl:ENSG00000233901 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129339532..129340982 26863196 MeRIP-seq:(Medium) rs879897451 Functional Loss SNV dbSNP153 33..33 33 - - - 107468 RMVar_ID_107468 Human_SNP_ID_416154797 m1A Human chr9 - 129340574 129340563 129340575 TATGTGCCAACTCACATGCCAACTCACACACGAACTCACACACCAACTCACATGCACACCAACTC TATGTGCCAACTCACATGCCAACTCACACAC____________CAACTCACATGCACACCAACTC GGTGTGTGAGTTC G lnc-IER5L-1,lnc-IER5L-1:2,lnc-IER5L-1:3,lnc-IER5L-1:4 RNACentral:URS00008B81DB,RNACentral:URS00008B5C78,RNACentral:URS00008BE9C6,RNACentral:URS00008B75A0 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129340531..129340972 26863196 MeRIP-seq:(Medium) rs1564262172 Functional Loss DEL dbSNP153 32..43 33 - - - 107469 RMVar_ID_107469 Human_SNP_ID_416154804 m1A Human chr9 - 129340574 129340574 129340574 TATGTGCCAACTCACATGCCAACTCACACACGAACTCACACACCAACTCACATGCACACCAACTC TATGTGCCAACTCACATGCCAACTCACACACGTACTCACACACCAACTCACATGCACACCAACTC T A lnc-IER5L-1,lnc-IER5L-1:2,lnc-IER5L-1:3,lnc-IER5L-1:4 RNACentral:URS00008B81DB,RNACentral:URS00008B5C78,RNACentral:URS00008BE9C6,RNACentral:URS00008B75A0 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129340531..129340972 26863196 MeRIP-seq:(Medium) rs1177315200 Functional Loss SNV dbSNP153 33..33 33 - - - 107470 RMVar_ID_107470 Human_SNP_ID_416154805 m1A Human chr9 - 129340574 129340574 129340574 TATGTGCCAACTCACATGCCAACTCACACACGAACTCACACACCAACTCACATGCACACCAACTC TATGTGCCAACTCACATGCCAACTCACACACGGACTCACACACCAACTCACATGCACACCAACTC T C lnc-IER5L-1,lnc-IER5L-1:2,lnc-IER5L-1:3,lnc-IER5L-1:4 RNACentral:URS00008B81DB,RNACentral:URS00008B5C78,RNACentral:URS00008BE9C6,RNACentral:URS00008B75A0 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129340531..129340972 26863196 MeRIP-seq:(Medium) rs1177315200 Functional Loss SNV dbSNP153 33..33 33 - - - 107471 RMVar_ID_107471 Human_SNP_ID_416172377 m1A Human chr9 - 129406459 129406459 129406459 AAGCAGCGGGAATGGCGTGCCCAGCGGAGGGAACGGCCTATGCAAAGGATCTCGTGGTGGGAGAG AAGCAGCGGGAATGGCGTGCCCAGCGGAGGGAGCGGCCTATGCAAAGGATCTCGTGGTGGGAGAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129406374..129406485 26863196 MeRIP-seq:(Medium) rs1290316911 Functional Loss SNV dbSNP153 33..33 33 - - - 107472 RMVar_ID_107472 Human_SNP_ID_416173470 m1A Human chr9 - 129410342 129410342 129410342 TGATGGTGGTGGTGATGCTGATGGTGGTGGTGATGTTGATGGTGGTGGTGATGTTGATGGTGGTT TGATGGTGGTGGTGATGCTGATGGTGGTGGTGGTGTTGATGGTGGTGGTGATGTTGATGGTGGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129410286..129410465 26863196 MeRIP-seq:(Medium) rs62583999 Functional Loss SNV dbSNP153 33..33 33 - - - 107473 RMVar_ID_107473 Human_SNP_ID_416194320 m1A Human chr9 + 129471252 129471250 129471253 GCAGTGTGTATAGGAAAGGGTATCAGATGCAGAGGAGGGCATTGAGAGAGGAGGGATTGAGTCAT GCAGTGTGTATAGGAAAGGGTATCAGATGCA___GAGGGCATTGAGAGAGGAGGGATTGAGTCAT AGAG A lnc-NTMT1-7 RNACentral:URS0000D59EF2 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129471161..129471252 26863196 MeRIP-seq:(Medium) rs1483333278 Functional Loss DEL dbSNP153 32..34 33 - - - 107474 RMVar_ID_107474 Human_SNP_ID_416199289 m1A Human chr9 - 129489968 129489968 129489968 AGGTGGGGGAGTGAGAGCCAGAGCTCTCAACCAAGCCTCTGGGAGGCCGCAGGGCCTGGGATCGC AGGTGGGGGAGTGAGAGCCAGAGCTCTCAACCTAGCCTCTGGGAGGCCGCAGGGCCTGGGATCGC T A RF00017-4596 RNACentral:URS00009759B0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129489965..129490690 26863196 MeRIP-seq:(Medium) rs1301369459 Functional Loss SNV dbSNP153 33..33 33 - - - 107475 RMVar_ID_107475 Human_SNP_ID_416201558 m1A Human chr9 + 129498110 129498110 129498110 ACTCAGAATGGTAGGGACAAGAGTGGACACAGAAGCCGGTTGGGAGTGTGGCACTGAGATCCAGG ACTCAGAATGGTAGGGACAAGAGTGGACACAGTAGCCGGTTGGGAGTGTGGCACTGAGATCCAGG A T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129498063..129498377 26863196 MeRIP-seq:(Medium) rs532012731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5107020,Human_RBP_ID_5637015 RMVar_hsa_circ_27128 107476 RMVar_ID_107476 Human_SNP_ID_416201725 m1A Human chr9 + 129498767 129498764 129498768 TATGAGAGGGAGTGCGAGAGTGTGTGTGTATGAGTGTGTATATGAATGTGAGTGTGTGAGTATTC TATGAGAGGGAGTGCGAGAGTGTGTGTGTA____TGTGTATATGAATGTGAGTGTGTGAGTATTC ATGAG A LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:129498536..129498997;chr9:129496907..129502288 26863196 MeRIP-seq:(Medium) rs1389680843 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5309250,Human_RBP_ID_5658966,Human_RBP_ID_17323371,Human_RBP_ID_23117189,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107477 RMVar_ID_107477 Human_SNP_ID_416201747 m1A Human chr9 + 129498812 129498808 129498812 ATGTGAGTGTGTGAGTATTCGTGTGTGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAG ATGTGAGTGTGTGAGTATTCGTGTGTGTG____TGAGTGTGTGAGTGTATATGTGTGAGTGTGAG GTATA G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:129498562..129498942;chr9:129496896..129502302 26863196 MeRIP-seq:(Medium) rs34564163 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107478 RMVar_ID_107478 Human_SNP_ID_416201748 m1A Human chr9 + 129498812 129498808 129498812 ATGTGAGTGTGTGAGTATTCGTGTGTGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAG ATGTGAGTGTGTGAGTATTCGTGTGTGTGTA__TGAGTGTGTGAGTGTATATGTGTGAGTGTGAG GTATA GTA LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:129498562..129498942;chr9:129496896..129502302 26863196 MeRIP-seq:(Medium) rs34564163 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107479 RMVar_ID_107479 Human_SNP_ID_416201753 m1A Human chr9 + 129498812 129498812 129498812 ATGTGAGTGTGTGAGTATTCGTGTGTGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAG ATGTGAGTGTGTGAGTATTCGTGTGTGTGTATGTGAGTGTGTGAGTGTATATGTGTGAGTGTGAG A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:129498562..129498942;chr9:129496896..129502302 26863196 MeRIP-seq:(Medium) rs371867854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107480 RMVar_ID_107480 Human_SNP_ID_416201760 m1A Human chr9 + 129498837 129498817 129498837 TGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTATATGAGT____________________GTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTGAGTGTATATGTGTGA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:129498726..129498934 26863196 MeRIP-seq:(Medium) rs902252097 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_17323372,Human_RBP_ID_23117190,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107481 RMVar_ID_107481 Human_SNP_ID_416201773 m1A Human chr9 + 129498837 129498831 129498837 TGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTATATGAGTGTGTGAGTGTATAT______GTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTGA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:129498726..129498934 26863196 MeRIP-seq:(Medium) rs968031844 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_17323372,Human_RBP_ID_23117190,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107482 RMVar_ID_107482 Human_SNP_ID_416201775 m1A Human chr9 + 129498837 129498833 129498837 TGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTATATGAGTGTGTGAGTGTATATGT____GTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:129498726..129498934 26863196 MeRIP-seq:(Medium) rs796183068 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_17323372,Human_RBP_ID_23117190,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107483 RMVar_ID_107483 Human_SNP_ID_416201777 m1A Human chr9 + 129498837 129498835 129498837 TGTGTATATGAGTGTGTGAGTGTATATGTGTGAGTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGTGTATATGAGTGTGTGAGTGTATATGTGT__GTGTGAGTGTATATGTGTGTGAGTGTGAATGT TGA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:129498726..129498934 26863196 MeRIP-seq:(Medium) rs1183008621 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5309251,Human_RBP_ID_17323372,Human_RBP_ID_23117190,Human_RBP_ID_24316674 RMVar_hsa_circ_27128 107484 RMVar_ID_107484 Human_SNP_ID_416202636 m1A Human chr9 - 129502139 129502130 129502140 GGGATAAGTCCCAGCTCTCAACCTGGCACTCGACGGCCTTCCTGATCAGCTGGGCTCCAGCCTCG GGGATAAGTCCCAGCTCTCAACCTGGCACTC__________CTGATCAGCTGGGCTCCAGCCTCG GGAAGGCCGTC G RF00017-4596 RNACentral:URS00009759B0 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129502131..129502217 26863196 MeRIP-seq:(Medium) rs1381392542 Functional Loss DEL dbSNP153 32..41 33 - - - 107485 RMVar_ID_107485 Human_SNP_ID_416203236 m1A Human chr9 + 129504142 129504142 129504142 CAGAATTTTCCCAGTTGTAGAAAGATGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAT CAGAATTTTCCCAGTTGTAGAAAGATGGGGCCCGGTGCAGTGGCTCACGCCTGTAATCCCAGCAT A C LINC00963 Ensembl:ENSG00000204054 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1231434535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089517,Human_Splice_Rec_1089551 RMVar_hsa_circ_77715,RMVar_hsa_circ_373652,RMVar_hsa_circ_260240,RMVar_hsa_circ_260241 107486 RMVar_ID_107486 Human_SNP_ID_416204649 m1A Human chr9 + 129508897 129508897 129508897 TGGGAGCTTCCCAGAGAAGGGATGATTGAGCTAAGTCTAAGCAAAAGGGGTGGTCAGGGCAGCAG TGGGAGCTTCCCAGAGAAGGGATGATTGAGCTGAGTCTAAGCAAAAGGGGTGGTCAGGGCAGCAG A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129508846..129509036 26863196 MeRIP-seq:(Medium) rs959835777 Functional Loss SNV dbSNP153 33..33 33 - - - 107487 RMVar_ID_107487 Human_SNP_ID_416231005 m1A Human chr9 + 129610134 129610134 129610134 TGGTCTGCGGGGAGGGAGTGGACAGCGCAGGGAGCGGACAGGAGCGCTGCGGGATCCCGGGGCCT TGGTCTGCGGGGAGGGAGTGGACAGCGCAGGGGGCGGACAGGAGCGCTGCGGGATCCCGGGGCCT A G NTMT1 Ensembl:ENSG00000148335 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129610052..129610180 26863196 MeRIP-seq:(Medium) rs1400095340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3907097,Human_RBP_ID_8223446,Human_RBP_ID_8731309,Human_RBP_ID_9441759,Human_RBP_ID_22733473 107488 RMVar_ID_107488 Human_SNP_ID_416235592 m1A Human chr9 - 129626249 129626245 129626249 CCCGGGACCGAGAGAAGAAGATGGGGAAGAGGAAGGGAGGGCGGCGGCGGCGGAGACGCCACAAG CCCGGGACCGAGAGAAGAAGATGGGGAAGAGG____GAGGGCGGCGGCGGCGGAGACGCCACAAG CCCTT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129626201..129626334 26863196 MeRIP-seq:(Medium) rs1373602261 Functional Loss DEL dbSNP153 33..36 33 - - - 107489 RMVar_ID_107489 Human_SNP_ID_416235600 m1A Human chr9 - 129626263 129626260 129626263 TCCGGGCGGGGGCTCCCGGGACCGAGAGAAGAAGATGGGGAAGAGGAAGGGAGGGCGGCGGCGGC TCCGGGCGGGGGCTCCCGGGACCGAGAGAAGA___TGGGGAAGAGGAAGGGAGGGCGGCGGCGGC ATCT A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:129626175..129626262 26863410 MeRIP-seq:(Medium) rs1278644166 Functional Loss DEL dbSNP153 33..35 33 - - - 107490 RMVar_ID_107490 Human_SNP_ID_416235608 m1A Human chr9 + 129626282 129626282 129626282 CCTCTTCCCCATCTTCTTCTCTCGGTCCCGGGAGCCCCCGCCCGGAGTGAGTAGCGCGAGGCGGT CCTCTTCCCCATCTTCTTCTCTCGGTCCCGGGTGCCCCCGCCCGGAGTGAGTAGCGCGAGGCGGT A T NTMT1 Ensembl:ENSG00000148335 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129626201..129626468 32194978 MeRIP-seq:(Medium) rs1447216768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256095,Human_RBP_ID_5036497,Human_RBP_ID_5410167,Human_RBP_ID_19144072 Human_Splice_Rec_1089787,Human_Splice_Rec_1089791,Human_Splice_Rec_1089797,Human_Splice_Rec_1089803,Human_Splice_Rec_1089809,Human_Splice_Rec_1089811,Human_Splice_Rec_1089815 RMVar_hsa_circ_98299,RMVar_hsa_circ_260242 107491 RMVar_ID_107491 Human_SNP_ID_416237227 m1A Human chr9 + 129632707 129632707 129632707 GCTTGAGTAGAGCCGTGGTTGGTGACAGCATGACGAGCGAGGTGATAGAAGACGAGAAGCAATTC GCTTGAGTAGAGCCGTGGTTGGTGACAGCATGGCGAGCGAGGTGATAGAAGACGAGAAGCAATTC A G NTMT1 Ensembl:ENSG00000148335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:129632602..129632897;chr9:129632619..129632894;chr9:129632604..129632825 26863196 MeRIP-seq:(Medium) rs979818468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2061330,Human_RBP_ID_5013310 Human_Splice_Rec_1089776,Human_Splice_Rec_1089782,Human_Splice_Rec_1089792,Human_Splice_Rec_1089798,Human_Splice_Rec_1089804,Human_Splice_Rec_1089805,Human_Splice_Rec_1089810,Human_Splice_Rec_1089816,Human_Splice_Rec_1089826,Human_Splice_Rec_1089827 RMVar_hsa_circ_8955,RMVar_hsa_circ_99157,RMVar_hsa_circ_98299,RMVar_hsa_circ_260242,RMVar_hsa_circ_45601,RMVar_hsa_circ_260243 107492 RMVar_ID_107492 Human_SNP_ID_416238130 m1A Human chr9 + 129635406 129635401 129635406 CTGCAGTGCAGGCCTCAGCCTCCTGGCCGAGGAGAGGCAGGAGAACCTCCCCGATGAGATCTACC CTGCAGTGCAGGCCTCAGCCTCCTGGCC_____GAGGCAGGAGAACCTCCCCGATGAGATCTACC CGAGGA C NTMT1 Ensembl:ENSG00000148335 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129635355..129635548 26863196 MeRIP-seq:(Medium) rs776328397 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_5124058,Human_RBP_ID_9233410,Human_RBP_ID_9408721,Human_RBP_ID_21906734 RMVar_hsa_circ_99157,RMVar_hsa_circ_98299,RMVar_hsa_circ_260242,RMVar_hsa_circ_260243 107493 RMVar_ID_107493 Human_SNP_ID_416239103 m1A Human chr9 + 129638382 129638382 129638382 TGATCATCTGGGCCTCCTCTTTGTCCCCTCCCACGGTCTCACCAAGCAGGAAGATGATGCAGGTG TGATCATCTGGGCCTCCTCTTTGTCCCCTCCCGCGGTCTCACCAAGCAGGAAGATGATGCAGGTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129638280..129638644 32194978 MeRIP-seq:(Medium) rs1196491144 Functional Loss SNV dbSNP153 33..33 33 - - - 107494 RMVar_ID_107494 Human_SNP_ID_416240393 m1A Human chr9 + 129642105 129642105 129642105 CTCCGGCGGCCGCGGACCCCACCTGCTCCGCCAGTCCAGCCCCTGCGCCCGGCCGGGTCCGCTCC CTCCGGCGGCCGCGGACCCCACCTGCTCCGCCGGTCCAGCCCCTGCGCCCGGCCGGGTCCGCTCC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:129642004..129642118;chr9:129641949..129642155;chr9:129641998..129642125 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1470305254 Functional Loss SNV dbSNP153 33..33 33 - - - 107495 RMVar_ID_107495 Human_SNP_ID_416240397 m1A Human chr9 + 129642110 129642110 129642110 GCGGCCGCGGACCCCACCTGCTCCGCCAGTCCAGCCCCTGCGCCCGGCCGGGTCCGCTCCTCAGT GCGGCCGCGGACCCCACCTGCTCCGCCAGTCCGGCCCCTGCGCCCGGCCGGGTCCGCTCCTCAGT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129641986..129642141 26863196 MeRIP-seq:(Medium) rs1184992913 Functional Loss SNV dbSNP153 33..33 33 - - - 107496 RMVar_ID_107496 Human_SNP_ID_416247104 m1A Human chr9 + 129665956 129665956 129665956 GCCGCCGCCTCCACCCGCGCTGGGGCCCGGCGACTGCGCCCAGGCGCGCAAGAACTTCTCGGTGA GCCGCCGCCTCCACCCGCGCTGGGGCCCGGCGGCTGCGCCCAGGCGCGCAAGAACTTCTCGGTGA A G PRRX2 Ensembl:ENSG00000167157 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129665608..129719279 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 107497 RMVar_ID_107497 Human_SNP_ID_416247105 m1A Human chr9 + 129665956 129665956 129665956 GCCGCCGCCTCCACCCGCGCTGGGGCCCGGCGACTGCGCCCAGGCGCGCAAGAACTTCTCGGTGA GCCGCCGCCTCCACCCGCGCTGGGGCCCGGCGTCTGCGCCCAGGCGCGCAAGAACTTCTCGGTGA A T PRRX2 Ensembl:ENSG00000167157 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129665608..129719279 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 107498 RMVar_ID_107498 Human_SNP_ID_416262289 m1A Human chr9 - 129720747 129720747 129720747 CTCACCTGTAGGGGGACGAGGCTGTCCAGGAGAGATAATCTGGACTCAGGGCGGTGGGCCGGGGA CTCACCTGTAGGGGGACGAGGCTGTCCAGGAGTGATAATCTGGACTCAGGGCGGTGGGCCGGGGA T A RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:129720697..129722286 32194978 MeRIP-seq:(Medium) rs569824624 Functional Loss SNV dbSNP153 33..33 33 - - - 107499 RMVar_ID_107499 Human_SNP_ID_416288492 m1A Human chr9 + 129815019 129815019 129815019 TGAATGCGGGCTGGCTCTGCACTGACCCGTCCACTCCTCCTGGGCTCCTGGAACTCCTGACCCAG TGAATGCGGGCTGGCTCTGCACTGACCCGTCCGCTCCTCCTGGGCTCCTGGAACTCCTGACCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129815000..129815224 26863196 MeRIP-seq:(Medium) rs936141228 Functional Loss SNV dbSNP153 33..33 33 - - - 107500 RMVar_ID_107500 Human_SNP_ID_416292518 m1A Human chr9 + 129829230 129829230 129829230 CACTCACGCTCAGGCTCTGGCTTCTCCGTGTCACCTACTCTCAAGGGCCGGGCCTTGGGCTCTTC CACTCACGCTCAGGCTCTGGCTTCTCCGTGTCGCCTACTCTCAAGGGCCGGGCCTTGGGCTCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129829199..129829313 26863196 MeRIP-seq:(Medium) rs3818553 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Clinvar_Rec_690,Clinvar_Rec_7102 GWAS_ID_14739,GWAS_ID_14740,GWAS_ID_14741,GWAS_ID_14742,GWAS_ID_14743,GWAS_ID_14744,GWAS_ID_14745,GWAS_ID_14746,GWAS_ID_14747,GWAS_ID_14748,GWAS_ID_14749,GWAS_ID_14750,GWAS_ID_14751,GWAS_ID_14752,GWAS_ID_14753,GWAS_ID_14754,GWAS_ID_14755,GWAS_ID_14756,GWAS_ID_14757,GWAS_ID_14758,GWAS_ID_14759,GWAS_ID_14760,GWAS_ID_14761,GWAS_ID_14762,GWAS_ID_14763,GWAS_ID_14764,GWAS_ID_14765,GWAS_ID_14766,GWAS_ID_14767,GWAS_ID_14768,GWAS_ID_14769,GWAS_ID_14770,GWAS_ID_14771,GWAS_ID_14772,GWAS_ID_14773,GWAS_ID_14774,GWAS_ID_14775,GWAS_ID_14776,GWAS_ID_14777,GWAS_ID_14778,GWAS_ID_14779,GWAS_ID_14780,GWAS_ID_14781,GWAS_ID_14782,GWAS_ID_14783,GWAS_ID_14784,GWAS_ID_14785,GWAS_ID_14786,GWAS_ID_14787,GWAS_ID_14788,GWAS_ID_14789,GWAS_ID_14790,GWAS_ID_14791,GWAS_ID_14792,GWAS_ID_14793,GWAS_ID_14794,GWAS_ID_14795,GWAS_ID_14796,GWAS_ID_14797,GWAS_ID_14798,GWAS_ID_14799,GWAS_ID_14800 107501 RMVar_ID_107501 Human_SNP_ID_416292549 m1A Human chr9 - 129829300 129829300 129829300 AACGTGTCCCCTGGTCTCTTTGGGTCCAGTTTATCATGAGGAGCTCAACGCGCCCATACGGAGAA AACGTGTCCCCTGGTCTCTTTGGGTCCAGTTTGTCATGAGGAGCTCAACGCGCCCATACGGAGAA T C C9orf78 Ensembl:ENSG00000136819 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129829298..129829401 26863196 MeRIP-seq:(Medium) rs1161028595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92460,Human_RBP_ID_23094519,Human_RBP_ID_26361246 Human_Splice_Rec_1089956,Human_Splice_Rec_1089957,Human_Splice_Rec_1089966,Human_Splice_Rec_1089967,Human_Splice_Rec_1089976,Human_Splice_Rec_1089978,Human_Splice_Rec_1089990 RMVar_hsa_circ_30990 107502 RMVar_ID_107502 Human_SNP_ID_416293031 m1A Human chr9 - 129831063 129831063 129831063 CTGAGGCCTCTGGGTTTCTCACTTCAGGATGAAGTACATTGAGACAGAGCTAAAGAAGAGGAAAG CTGAGGCCTCTGGGTTTCTCACTTCAGGATGAGGTACATTGAGACAGAGCTAAAGAAGAGGAAAG T C C9orf78 Ensembl:ENSG00000136819 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:129830926..129831441;chr9:129830926..129831123 26863196 MeRIP-seq:(Medium) rs1265098775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713335,Human_RBP_ID_3190691,Human_RBP_ID_26361250 Human_Splice_Rec_1089952,Human_Splice_Rec_1089972,Human_Splice_Rec_1089986,Human_Splice_Rec_1089998 RMVar_hsa_circ_30990 107503 RMVar_ID_107503 Human_SNP_ID_416293032 m1A Human chr9 - 129831067 129831067 129831067 CTCCCTGAGGCCTCTGGGTTTCTCACTTCAGGATGAAGTACATTGAGACAGAGCTAAAGAAGAGG CTCCCTGAGGCCTCTGGGTTTCTCACTTCAGGGTGAAGTACATTGAGACAGAGCTAAAGAAGAGG T C C9orf78 Ensembl:ENSG00000136819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129831018..129831109 26863196 MeRIP-seq:(Medium) rs1216915594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3190691,Human_RBP_ID_26361250 Human_Splice_Rec_1089952,Human_Splice_Rec_1089972,Human_Splice_Rec_1089986,Human_Splice_Rec_1089998 RMVar_hsa_circ_30990 107504 RMVar_ID_107504 Human_SNP_ID_416293776 m1A Human chr9 - 129833466 129833466 129833466 AGACAGGTGGTATGGTGGATATGAAGAAACTGAAGGAAAGGGGCAAAGATAAGTAAGTTCAGGAC AGACAGGTGGTATGGTGGATATGAAGAAACTGCAGGAAAGGGGCAAAGATAAGTAAGTTCAGGAC T G C9orf78 Ensembl:ENSG00000136819 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129831857..129833576 26863196 MeRIP-seq:(Medium) rs761692637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8239069,Human_RBP_ID_23117270,Human_RBP_ID_26361252,Human_RBP_ID_27832847 Human_Splice_Rec_1089948,Human_Splice_Rec_1089949,Human_Splice_Rec_1089969,Human_Splice_Rec_1089982,Human_Splice_Rec_1089983,Human_Splice_Rec_1089994,Human_Splice_Rec_1089995,Human_Splice_Rec_1089999 107505 RMVar_ID_107505 Human_SNP_ID_416294309 m1A Human chr9 - 129835145 129835145 129835145 GGAGTCAGAGGAAGATGAGCAGGACTCAGAGGAGGTTCGGTGCGTTTGGGGCGGGGCTCCCATAG GGAGTCAGAGGAAGATGAGCAGGACTCAGAGGCGGTTCGGTGCGTTTGGGGCGGGGCTCCCATAG T G C9orf78 Ensembl:ENSG00000136819 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:129835132..129835269 26863196 MeRIP-seq:(Medium) rs772233601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036504,Human_RBP_ID_5633761,Human_RBP_ID_7902020,Human_RBP_ID_9407641,Human_RBP_ID_19146097,Human_RBP_ID_22118935,Human_RBP_ID_23094852,Human_RBP_ID_26361258 Human_Splice_Rec_1089943,Human_Splice_Rec_1089959,Human_Splice_Rec_1089991 107506 RMVar_ID_107506 Human_SNP_ID_416315065 m1A Human chr9 + 129908997 129908997 129908997 GGTGGGAGGTTGCTGAAATCCTCCGGTGTTGCACCCTGCAGACACAAATATAAATGAGAAACCAG GGTGGGAGGTTGCTGAAATCCTCCGGTGTTGCCCCCTGCAGACACAAATATAAATGAGAAACCAG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129908948..129909037 26863196 MeRIP-seq:(Medium) rs779882599 Functional Loss SNV dbSNP153 33..33 33 - - - 107507 RMVar_ID_107507 Human_SNP_ID_416318804 m1A Human chr9 - 129923896 129923896 129923896 GCAAAAGGAACCCCTCTCCCATCGCTTCAACGAGTTCATGACCTCCAAACCCAAAATCCACTGCT GCAAAAGGAACCCCTCTCCCATCGCTTCAACGGGTTCATGACCTCCAAACCCAAAATCCACTGCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129923845..129924983 26863196 MeRIP-seq:(Medium) rs368984808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1119511,Human_RBP_ID_18963128 Human_Splice_Rec_1090213,Human_Splice_Rec_1090273,Human_Splice_Rec_1090301,Human_Splice_Rec_1090328,Human_Splice_Rec_1090329 RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_363513,RMVar_hsa_circ_27140,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_378645,RMVar_hsa_circ_74258,RMVar_hsa_circ_260275,RMVar_hsa_circ_114146,RMVar_hsa_circ_333687,RMVar_hsa_circ_81238,RMVar_hsa_circ_260277,RMVar_hsa_circ_292978,RMVar_hsa_circ_52775,RMVar_hsa_circ_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278,RMVar_hsa_circ_271812,RMVar_hsa_circ_359498,RMVar_hsa_circ_260282 107508 RMVar_ID_107508 Human_SNP_ID_416321107 m1A Human chr9 - 129932718 129932718 129932718 ACAGGAAGAAGCAGACGCCAAGGCATATGGTCAGGAAGGGAGTTAACAGGCCACCAACAAAGAGG ACAGGAAGAAGCAGACGCCAAGGCATATGGTCGGGAAGGGAGTTAACAGGCCACCAACAAAGAGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:129932696..129932864 26863196 MeRIP-seq:(Medium) rs1048690547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29935,RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_260275,RMVar_hsa_circ_114146,RMVar_hsa_circ_81238,RMVar_hsa_circ_260278,RMVar_hsa_circ_359498,RMVar_hsa_circ_46271,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_269261,RMVar_hsa_circ_260284 107509 RMVar_ID_107509 Human_SNP_ID_416359537 m1A Human chr9 + 130085066 130085066 130085066 AGAGAGAGGTCTTAGATAATATAGGGCCAAGCAATAGAGGAATTGATGAGCAGGCTACGGGAAGT AGAGAGAGGTCTTAGATAATATAGGGCCAAGCTATAGAGGAATTGATGAGCAGGCTACGGGAAGT A T GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130085058..130085331 26863196 MeRIP-seq:(Medium) rs1001820649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21531,RMVar_hsa_circ_41437,RMVar_hsa_circ_340650,RMVar_hsa_circ_320368,RMVar_hsa_circ_45863,RMVar_hsa_circ_260291,RMVar_hsa_circ_343175,RMVar_hsa_circ_260293,RMVar_hsa_circ_52821,RMVar_hsa_circ_302690,RMVar_hsa_circ_260296,RMVar_hsa_circ_113198,RMVar_hsa_circ_326380,RMVar_hsa_circ_346956,RMVar_hsa_circ_260294,RMVar_hsa_circ_337763,RMVar_hsa_circ_316315,RMVar_hsa_circ_278733,RMVar_hsa_circ_305589,RMVar_hsa_circ_277072,RMVar_hsa_circ_260298,RMVar_hsa_circ_260300,RMVar_hsa_circ_22432,RMVar_hsa_circ_260299,RMVar_hsa_circ_260297,RMVar_hsa_circ_35701,RMVar_hsa_circ_302307,RMVar_hsa_circ_10910 107510 RMVar_ID_107510 Human_SNP_ID_416385016 m1A Human chr9 - 130181733 130181733 130181733 GCAGCACCCGCCCTGCCTGCAACACCCACACCAGGCACCCGGGCCCGCTCACGCTCACCTGCACA GCAGCACCCGCCCTGCCTGCAACACCCACACCTGGCACCCGGGCCCGCTCACGCTCACCTGCACA T A RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130181606..130181906 26863196 MeRIP-seq:(Medium) rs966013157 Functional Loss SNV dbSNP153 33..33 33 - - - 107511 RMVar_ID_107511 Human_SNP_ID_416388349 m1A Human chr9 - 130193211 130193211 130193211 ACAGCACCCCGCAGCTGTGTTCTCCCTGCAGTACCTCAGAGCCCCCTCGGTACCATCTCCTGAGA ACAGCACCCCGCAGCTGTGTTCTCCCTGCAGTCCCTCAGAGCCCCCTCGGTACCATCTCCTGAGA T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130193209..130193842 26863196 MeRIP-seq:(Medium) rs1269280916 Functional Loss SNV dbSNP153 33..33 33 - - - 107512 RMVar_ID_107512 Human_SNP_ID_416388377 m1A Human chr9 - 130193347 130193347 130193347 CCATCCCACTTTCCCATCCAGTCCCCACCTGCAGCTGCCAGCATCCCTAATGTGGTCACATTCCT CCATCCCACTTTCCCATCCAGTCCCCACCTGCGGCTGCCAGCATCCCTAATGTGGTCACATTCCT T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130193317..130193446 26863196 MeRIP-seq:(Medium) rs973884590 Functional Loss SNV dbSNP153 33..33 33 - - - 107513 RMVar_ID_107513 Human_SNP_ID_416388471 m1A Human chr9 - 130193639 130193639 130193639 AGTCTCCTCCCAGCTGGCCCCTCCTGCAGTTCAGCTCCCCCACCCCCGTCCAAGCTCCTCACCGA AGTCTCCTCCCAGCTGGCCCCTCCTGCAGTTCGGCTCCCCCACCCCCGTCCAAGCTCCTCACCGA T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130193635..130193729 26863196 MeRIP-seq:(Medium) rs1322916281 Functional Loss SNV dbSNP153 33..33 33 - - - 107514 RMVar_ID_107514 Human_SNP_ID_416388641 m1A Human chr9 + 130194289 130194289 130194289 TCCTGGCAGACAAGGGCTGTGTGGAAGGGAGGAGGAGCTGGAGTAGAGGAGCTGGGGACCTCAGG TCCTGGCAGACAAGGGCTGTGTGGAAGGGAGGGGGAGCTGGAGTAGAGGAGCTGGGGACCTCAGG A G NCS1 Ensembl:ENSG00000107130 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130194287..130194396 26863196 MeRIP-seq:(Medium) rs1257250804 Functional Loss SNV dbSNP153 33..33 33 - - - 107515 RMVar_ID_107515 Human_SNP_ID_416393751 m1A Human chr9 - 130214093 130214093 130214093 TGTAGGCCCCCTGACACCGCTGTGCCCTGATGACCCGCATGAGGCCTGGCATGTAACATGGTCCT TGTAGGCCCCCTGACACCGCTGTGCCCTGATGGCCCGCATGAGGCCTGGCATGTAACATGGTCCT T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130214090..130214204 26863196 MeRIP-seq:(Medium) rs372008012 Functional Loss SNV dbSNP153 33..33 33 - - - 107516 RMVar_ID_107516 Human_SNP_ID_416398893 m1A Human chr9 + 130233047 130233047 130233047 CTGTGCCATGAGGCCACCTCAGCCCTGACACCAACCCCGTGCGTCCACCCAGCCTTCTTCCGCAT CTGTGCCATGAGGCCACCTCAGCCCTGACACCTACCCCGTGCGTCCACCCAGCCTTCTTCCGCAT A T NCS1 Ensembl:ENSG00000107130 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:130232955..130233225 26863196 MeRIP-seq:(Medium) rs954580607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5014094 Human_Splice_Rec_1090556,Human_Splice_Rec_1090574 107517 RMVar_ID_107517 Human_SNP_ID_416399783 m1A Human chr9 - 130235949 130235949 130235949 CCATCAACACAAAGTGAGGAGCAGACGCTACGAGGAAGAGGACAGGCCGTGGCCGACTGGCCGCC CCATCAACACAAAGTGAGGAGCAGACGCTACGCGGAAGAGGACAGGCCGTGGCCGACTGGCCGCC T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:130235901..130235950 32194978 MeRIP-seq:(Medium) rs1362198924 Functional Loss SNV dbSNP153 33..33 33 - - - 107518 RMVar_ID_107518 Human_SNP_ID_416457820 m1A Human chr9 + 130454750 130454747 130454751 ATCCATCGATCCATCCATCCATCCATTCAGCCATCCATCCATCCATCACCCACCCATCCATTCAC ATCCATCGATCCATCCATCCATCCATTCAG____CCATCCATCCATCACCCACCCATCCATTCAC GCCAT G ASS1 Ensembl:ENSG00000130707 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130454747..130454877 26863196 MeRIP-seq:(Medium) rs1165812230 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_3191003 RMVar_hsa_circ_75242,RMVar_hsa_circ_77771,RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317,RMVar_hsa_circ_260319,RMVar_hsa_circ_291752,RMVar_hsa_circ_366782,RMVar_hsa_circ_375715,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_260321,RMVar_hsa_circ_33466,RMVar_hsa_circ_60006,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_260325,RMVar_hsa_circ_77734,RMVar_hsa_circ_260320,RMVar_hsa_circ_307299,RMVar_hsa_circ_44540,RMVar_hsa_circ_260324 107519 RMVar_ID_107519 Human_SNP_ID_416458835 m1A Human chr9 + 130458546 130458546 130458546 CTGCATCGCCCGCAAACAAGTGGAAATCGCCCAGCGGGAGGGGGCCAAGTATGTGTCCCACGGCG CTGCATCGCCCGCAAACAAGTGGAAATCGCCCGGCGGGAGGGGGCCAAGTATGTGTCCCACGGCG A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130458392..130458636 26863196 MeRIP-seq:(Medium) rs149602848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8698061 Human_Splice_Rec_1090871,Human_Splice_Rec_1090901,Human_Splice_Rec_1090931,Human_Splice_Rec_1090959,Human_Splice_Rec_1090971,Human_Splice_Rec_1090977 RMVar_hsa_circ_75242,RMVar_hsa_circ_77771,RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317,RMVar_hsa_circ_260319,RMVar_hsa_circ_291752,RMVar_hsa_circ_366782,RMVar_hsa_circ_375715,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_260321,RMVar_hsa_circ_33466,RMVar_hsa_circ_60006,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_260325,RMVar_hsa_circ_77734,RMVar_hsa_circ_260320,RMVar_hsa_circ_307299,RMVar_hsa_circ_44540,RMVar_hsa_circ_314888,RMVar_hsa_circ_365781,RMVar_hsa_circ_260324,RMVar_hsa_circ_369228,RMVar_hsa_circ_318975,RMVar_hsa_circ_284089,RMVar_hsa_circ_260326,RMVar_hsa_circ_31218,RMVar_hsa_circ_260327 107520 RMVar_ID_107520 Human_SNP_ID_416460215 m1A Human chr9 + 130463970 130463970 130463970 TCTCCCTCCTGCCACATGCCCACACATACACGACCTACACTGCATGACCTCACATGTGTACACGC TCTCCCTCCTGCCACATGCCCACACATACACGTCCTACACTGCATGACCTCACATGTGTACACGC A T ASS1 Ensembl:ENSG00000130707 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130463968..130464218 26863196 MeRIP-seq:(Medium) rs1190147595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26207471 RMVar_hsa_circ_75242,RMVar_hsa_circ_77771,RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317,RMVar_hsa_circ_260319,RMVar_hsa_circ_366782,RMVar_hsa_circ_375715,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_260321,RMVar_hsa_circ_33466,RMVar_hsa_circ_60006,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_77734,RMVar_hsa_circ_44540,RMVar_hsa_circ_314888,RMVar_hsa_circ_365781,RMVar_hsa_circ_260324,RMVar_hsa_circ_369228,RMVar_hsa_circ_284089,RMVar_hsa_circ_31218,RMVar_hsa_circ_260327 107521 RMVar_ID_107521 Human_SNP_ID_416461048 m1A Human chr9 + 130466776 130466776 130466776 TGCCTGAATTCTACAACCGGTTCAAGGGCCGCAATGACCTGATGGAGTACGCAAAGGTATGGCCG TGCCTGAATTCTACAACCGGTTCAAGGGCCGCGATGACCTGATGGAGTACGCAAAGGTATGGCCG A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:130466751..130466775 26863196 MeRIP-seq:(Medium) rs1199062770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713518,Human_RBP_ID_1058215,Human_RBP_ID_18140690,Human_RBP_ID_19024459,Human_RBP_ID_26207474,Human_RBP_ID_27162566 Human_Splice_Rec_1090874,Human_Splice_Rec_1090875,Human_Splice_Rec_1090904,Human_Splice_Rec_1090905,Human_Splice_Rec_1090934,Human_Splice_Rec_1090935,Human_Splice_Rec_1090962,Human_Splice_Rec_1090963,Human_Splice_Rec_1090972,Human_Splice_Rec_1090973,Human_Splice_Rec_1090980,Human_Splice_Rec_1090981,Human_Splice_Rec_1090989 Human_miRNA_ID_2938517 RMVar_hsa_circ_75242,RMVar_hsa_circ_77771,RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317,RMVar_hsa_circ_260319,RMVar_hsa_circ_366782,RMVar_hsa_circ_375715,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_260321,RMVar_hsa_circ_33466,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_77734,RMVar_hsa_circ_44540,RMVar_hsa_circ_314888,RMVar_hsa_circ_365781,RMVar_hsa_circ_260324,RMVar_hsa_circ_369228,RMVar_hsa_circ_73943,RMVar_hsa_circ_31218,RMVar_hsa_circ_127273,RMVar_hsa_circ_366636,RMVar_hsa_circ_70354,RMVar_hsa_circ_260328 107522 RMVar_ID_107522 Human_SNP_ID_416462147 m1A Human chr9 + 130470879 130470879 130470879 CCATCCCGGTCACTCCCAAGAACCCGTGGAGCATGGATGAGAACCTCATGCACATCAGGTAAATC CCATCCCGGTCACTCCCAAGAACCCGTGGAGCGTGGATGAGAACCTCATGCACATCAGGTAAATC A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:130470876..130470925 26863196 MeRIP-seq:(Medium) rs1391150004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1090876,Human_Splice_Rec_1090877,Human_Splice_Rec_1090906,Human_Splice_Rec_1090907,Human_Splice_Rec_1090936,Human_Splice_Rec_1090937,Human_Splice_Rec_1090964,Human_Splice_Rec_1090965,Human_Splice_Rec_1090974,Human_Splice_Rec_1090975,Human_Splice_Rec_1090982,Human_Splice_Rec_1090983,Human_Splice_Rec_1090990,Human_Splice_Rec_1090991 Human_miRNA_ID_2896588 RMVar_hsa_circ_77771,RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317,RMVar_hsa_circ_260319,RMVar_hsa_circ_366782,RMVar_hsa_circ_375715,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_260321,RMVar_hsa_circ_33466,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_77734,RMVar_hsa_circ_44540,RMVar_hsa_circ_365781,RMVar_hsa_circ_260324,RMVar_hsa_circ_369228,RMVar_hsa_circ_31218,RMVar_hsa_circ_127273,RMVar_hsa_circ_366636,RMVar_hsa_circ_70354,RMVar_hsa_circ_260328 107523 RMVar_ID_107523 Human_SNP_ID_416463897 m1A Human chr9 + 130476912 130476912 130476912 CCTCCAGGTCTCTACACGAAGACCCAGGACCCAGCCAAAGCCCCCAACACCCCTGACATTCTCGA CCTCCAGGTCTCTACACGAAGACCCAGGACCCGGCCAAAGCCCCCAACACCCCTGACATTCTCGA A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr9:130476814..130477003;chr9:130476901..130476925 26863196 MeRIP-seq:(Medium) rs1417942006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27543012 Human_Splice_Rec_1090880,Human_Splice_Rec_1090881,Human_Splice_Rec_1090910,Human_Splice_Rec_1090911,Human_Splice_Rec_1090940,Human_Splice_Rec_1090941,Human_Splice_Rec_1090986,Human_Splice_Rec_1090987,Human_Splice_Rec_1090994,Human_Splice_Rec_1091000,Human_Splice_Rec_1091001,Human_Splice_Rec_1091007 RMVar_hsa_circ_366782,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_33466,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_44540,RMVar_hsa_circ_369228,RMVar_hsa_circ_31218,RMVar_hsa_circ_366636,RMVar_hsa_circ_70354,RMVar_hsa_circ_260330,RMVar_hsa_circ_309553,RMVar_hsa_circ_340138,RMVar_hsa_circ_260329 107524 RMVar_ID_107524 Human_SNP_ID_416467147 m1A Human chr9 + 130489387 130489387 130489387 CACCATCCTTTACCATGCTCATTTAGACATCGAGGCCTTCACCATGGACCGGGAAGTGCGCAAAA CACCATCCTTTACCATGCTCATTTAGACATCGGGGCCTTCACCATGGACCGGGAAGTGCGCAAAA A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130489299..130489518 26863196 MeRIP-seq:(Medium) rs372061654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713520 Human_Splice_Rec_1090886,Human_Splice_Rec_1090887,Human_Splice_Rec_1090916,Human_Splice_Rec_1090917,Human_Splice_Rec_1090946,Human_Splice_Rec_1090947,Human_Splice_Rec_1090998,Human_Splice_Rec_1091006,Human_Splice_Rec_1091012,Human_Splice_Rec_1091016,Human_Splice_Rec_1091017 RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_33466,RMVar_hsa_circ_260323,RMVar_hsa_circ_44540,RMVar_hsa_circ_48014,RMVar_hsa_circ_31218,RMVar_hsa_circ_260330,RMVar_hsa_circ_340138,RMVar_hsa_circ_305397,RMVar_hsa_circ_357781,RMVar_hsa_circ_260331 107525 RMVar_ID_107525 Human_SNP_ID_416468498 m1A Human chr9 + 130494938 130494938 130494938 GCATCGCCAAGTCCCAGGAGCGAGTGGAAGGGAAAGTGCAGGTGTCCGTCCTCAAGGGCCAGGTG GCATCGCCAAGTCCCAGGAGCGAGTGGAAGGGGAAGTGCAGGTGTCCGTCCTCAAGGGCCAGGTG A G ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130494835..130495072 26863196 MeRIP-seq:(Medium) rs1428619789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1090888,Human_Splice_Rec_1090889,Human_Splice_Rec_1090918,Human_Splice_Rec_1090919,Human_Splice_Rec_1090948,Human_Splice_Rec_1090949,Human_Splice_Rec_1091018,Human_Splice_Rec_1091019 Human_miRNA_ID_2134975 RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_33466,RMVar_hsa_circ_260323,RMVar_hsa_circ_44540,RMVar_hsa_circ_260330,RMVar_hsa_circ_340138,RMVar_hsa_circ_122563,RMVar_hsa_circ_305397,RMVar_hsa_circ_260331,RMVar_hsa_circ_371526,RMVar_hsa_circ_260333,RMVar_hsa_circ_98358,RMVar_hsa_circ_260334,RMVar_hsa_circ_260332 107526 RMVar_ID_107526 Human_SNP_ID_416468815 m1A Human chr9 + 130495737 130495737 130495737 AGTAGGTGGGAGGTGGAAGGGCACCTGTGGAAATGCGGTAGCTTGGACCATGCTGATGATTCCTG AGTAGGTGGGAGGTGGAAGGGCACCTGTGGAAGTGCGGTAGCTTGGACCATGCTGATGATTCCTG A G ASS1 Ensembl:ENSG00000130707 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130495735..130495952 26863196 MeRIP-seq:(Medium) rs1473606929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8698105 RMVar_hsa_circ_115689,RMVar_hsa_circ_260323,RMVar_hsa_circ_371526,RMVar_hsa_circ_260333,RMVar_hsa_circ_98358,RMVar_hsa_circ_260334 107527 RMVar_ID_107527 Human_SNP_ID_416470086 m1A Human chr9 + 130501033 130501033 130501033 AGCAAGGTCACTGCCAAATAGACCCGTGTACAATGAGGAGCTGGGGCCTCCTCAATTTGCAGATC AGCAAGGTCACTGCCAAATAGACCCGTGTACACTGAGGAGCTGGGGCCTCCTCAATTTGCAGATC A C ASS1 Ensembl:ENSG00000130707 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130500967..130501219 26863196 MeRIP-seq:(Medium) rs781440434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182974,Human_RBP_ID_17321384 Human_Splice_Rec_1090892,Human_Splice_Rec_1090922,Human_Splice_Rec_1090952,Human_Splice_Rec_1091022 RMVar_hsa_circ_98358,RMVar_hsa_circ_260334 107528 RMVar_ID_107528 Human_SNP_ID_416470087 m1A Human chr9 + 130501033 130501033 130501033 AGCAAGGTCACTGCCAAATAGACCCGTGTACAATGAGGAGCTGGGGCCTCCTCAATTTGCAGATC AGCAAGGTCACTGCCAAATAGACCCGTGTACAGTGAGGAGCTGGGGCCTCCTCAATTTGCAGATC A G ASS1 Ensembl:ENSG00000130707 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130500967..130501219 26863196 MeRIP-seq:(Medium) rs781440434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182974,Human_RBP_ID_17321384 Human_Splice_Rec_1090892,Human_Splice_Rec_1090922,Human_Splice_Rec_1090952,Human_Splice_Rec_1091022 RMVar_hsa_circ_98358,RMVar_hsa_circ_260334 107529 RMVar_ID_107529 Human_SNP_ID_416470367 m1A Human chr9 + 130501931 130501931 130501931 GGCCGAAGTGAGGACATGTAACACAGGCACTCACCGCTGGGATGCTGTGGACCTGGGGCACAGAG GGCCGAAGTGAGGACATGTAACACAGGCACTCGCCGCTGGGATGCTGTGGACCTGGGGCACAGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130501884..130502005 26863196 MeRIP-seq:(Medium) rs1480576184 Functional Loss SNV dbSNP153 33..33 33 - - - 107530 RMVar_ID_107530 Human_SNP_ID_416490662 m1A Human chr9 - 130579648 130579630 130579648 TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCG__________________CTCGGCTCCCCGGTC GCGGCGGCGTCGGCGGCGT G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130579601..130579755 26863196 MeRIP-seq:(Medium) rs537586454 Functional Loss DEL dbSNP153 33..50 33 - - - 107531 RMVar_ID_107531 Human_SNP_ID_416490663 m1A Human chr9 - 130579648 130579630 130579648 TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCG_________ACGCCGCCGCTCGGCTCCCCGGTC GCGGCGGCGTCGGCGGCGT GCGGCGGCGT RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130579601..130579755 26863196 MeRIP-seq:(Medium) rs537586454 Functional Loss DEL dbSNP153 33..41 33 - - - 107532 RMVar_ID_107532 Human_SNP_ID_416490675 m1A Human chr9 - 130579639 130579639 130579639 CGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTCCGGCCTCCC CGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGCCGCCGCCGCTCGGCTCCCCGGTCCGGCCTCCC T G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:130579576..130579821;chr9:130579576..130579752;chr9:130579576..130579860;chr9:130579576..130579940;chr9:130579551..130579991;chr9:130579576..130580702 26863196 MeRIP-seq:(Medium) rs1005562465 Functional Loss SNV dbSNP153 33..33 33 - - - 107533 RMVar_ID_107533 Human_SNP_ID_416490681 m1A Human chr9 - 130579648 130579642 130579648 TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCG______CCGACGCCGCCGCTCGGCTCCCCGGTC GCGGCGT G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130579601..130579755 26863196 MeRIP-seq:(Medium) rs1173164624 Functional Loss DEL dbSNP153 33..38 33 - - - 107534 RMVar_ID_107534 Human_SNP_ID_416490687 m1A Human chr9 - 130579648 130579648 130579648 TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGCCGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC T G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130579601..130579755 26863196 MeRIP-seq:(Medium) rs1207238854 Functional Loss SNV dbSNP153 33..33 33 - - - 107535 RMVar_ID_107535 Human_SNP_ID_416490766 m1A Human chr9 - 130579766 130579766 130579766 ATCTCGTGCTCCTGCCAGCCGGCTGCGCCCGTACCTGCCGGACCCGGTGCAGGGCATCCACGAAG ATCTCGTGCTCCTGCCAGCCGGCTGCGCCCGTCCCTGCCGGACCCGGTGCAGGGCATCCACGAAG T G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:130579658..130580702 32194978 MeRIP-seq:(Medium) rs528383748 Functional Loss SNV dbSNP153 33..33 33 - - - 107536 RMVar_ID_107536 Human_SNP_ID_416495096 m1A Human chr9 - 130595426 130595423 130595427 ACTCAGTAACAAACCATGGCTCTATCTGAGGGAGAAAGACAAGTGTCCTCTTTAAAGGGCTATTA ACTCAGTAACAAACCATGGCTCTATCTGAGG____AAGACAAGTGTCCTCTTTAAAGGGCTATTA TTCTC T RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130595423..130613018 26863196 MeRIP-seq:(Medium) rs1242135880 Functional Loss DEL dbSNP153 32..35 33 - - - 107537 RMVar_ID_107537 Human_SNP_ID_416495102 m1A Human chr9 + 130595438 130595438 130595438 AAAGAGGACACTTGTCTTTCTCCCTCAGATAGAGCCATGGTTTGTTACTGAGTGTTTAAATCTGA AAAGAGGACACTTGTCTTTCTCCCTCAGATAGTGCCATGGTTTGTTACTGAGTGTTTAAATCTGA A T FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130595437..130595525 26863196 MeRIP-seq:(Medium) rs1382164444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 107538 RMVar_ID_107538 Human_SNP_ID_416495105 m1A Human chr9 + 130595442 130595442 130595442 AGGACACTTGTCTTTCTCCCTCAGATAGAGCCATGGTTTGTTACTGAGTGTTTAAATCTGATTCT AGGACACTTGTCTTTCTCCCTCAGATAGAGCCGTGGTTTGTTACTGAGTGTTTAAATCTGATTCT A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130595439..130595600 26863196 MeRIP-seq:(Medium) rs374300531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 107539 RMVar_ID_107539 Human_SNP_ID_416501602 m1A Human chr9 - 130620405 130620405 130620405 TCGAGAGTTGAAATCGCCGCGTACACCCCGAAAGTCAGCTTGGTCTTTTTCTCGGATAATCTCTA TCGAGAGTTGAAATCGCCGCGTACACCCCGAATGTCAGCTTGGTCTTTTTCTCGGATAATCTCTA T A RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130620298..130620436 26863196 MeRIP-seq:(Medium) rs1347022383 Functional Loss SNV dbSNP153 33..33 33 - - - 107540 RMVar_ID_107540 Human_SNP_ID_416502498 m1A Human chr9 + 130623705 130623705 130623705 GCAGCGCATATCATCAGCGAGCTGATTCTTACAGCCCAGGTGGGTCCAGCTCTGCAGAGTGTGAG GCAGCGCATATCATCAGCGAGCTGATTCTTACGGCCCAGGTGGGTCCAGCTCTGCAGAGTGTGAG A G FUBP3 Ensembl:ENSG00000107164 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130623654..130623750 26863196 MeRIP-seq:(Medium) rs775045112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407656,Human_RBP_ID_19024462,Human_RBP_ID_26362253 Human_Splice_Rec_1091044,Human_Splice_Rec_1091045,Human_Splice_Rec_1091084,Human_Splice_Rec_1091085,Human_Splice_Rec_1091112,Human_Splice_Rec_1091113 Human_miRNA_ID_2553802 RMVar_hsa_circ_1641,RMVar_hsa_circ_87967,RMVar_hsa_circ_104170,RMVar_hsa_circ_260335,RMVar_hsa_circ_260337,RMVar_hsa_circ_7595,RMVar_hsa_circ_11720,RMVar_hsa_circ_375251,RMVar_hsa_circ_30949,RMVar_hsa_circ_102448,RMVar_hsa_circ_260340,RMVar_hsa_circ_118431,RMVar_hsa_circ_260341,RMVar_hsa_circ_260342 107541 RMVar_ID_107541 Human_SNP_ID_416503232 m1A Human chr9 - 130626411 130626411 130626411 CCAGGGGCTCCCACGCTCCAGTCGCCACGGCCACGACCTCTTCCTCTGGCTGCTGCCAGGCCTCC CCAGGGGCTCCCACGCTCCAGTCGCCACGGCCTCGACCTCTTCCTCTGGCTGCTGCCAGGCCTCC T A RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:130626331..130626547;chr9:130626315..130626543;chr9:130626299..130626549 26863196 MeRIP-seq:(Medium) rs533409196 Functional Loss SNV dbSNP153 33..33 33 - - - 107542 RMVar_ID_107542 Human_SNP_ID_416504898 m1A Human chr9 - 130631984 130631984 130631984 GGGGTGCTGTGGGGGTTCCCATTCACCTTGGCAGCCATGTTTGGGAAGCACCCGGAGCTCCTTGG GGGGTGCTGTGGGGGTTCCCATTCACCTTGGCCGCCATGTTTGGGAAGCACCCGGAGCTCCTTGG T G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130631210..130631984 26863196 MeRIP-seq:(Medium) rs1035587465 Functional Loss SNV dbSNP153 33..33 33 - - - 107543 RMVar_ID_107543 Human_SNP_ID_416506020 m1A Human chr9 + 130636023 130636017 130636023 TCAACCAGGTCACGCCGCCAGCGCTGCTCCTCAGGCCAGCTCCCCACCGGACTACACAATGGCCT TCAACCAGGTCACGCCGCCAGCGCTGC______GGCCAGCTCCCCACCGGACTACACAATGGCCT CTCCTCA C FUBP3 Ensembl:ENSG00000107164 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:130634651..130636076;chr9:130632201..130636150 26863196 MeRIP-seq:(Medium) rs1489860873 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_9407657,Human_RBP_ID_22690415,Human_RBP_ID_22748239 Human_Splice_Rec_1091058,Human_Splice_Rec_1091098,Human_Splice_Rec_1091124 Human_miRNA_ID_2367019,Human_miRNA_ID_2725634,Human_miRNA_ID_3014822 RMVar_hsa_circ_87967,RMVar_hsa_circ_104170,RMVar_hsa_circ_260335,RMVar_hsa_circ_260337,RMVar_hsa_circ_115078,RMVar_hsa_circ_260344,RMVar_hsa_circ_120595,RMVar_hsa_circ_260343,RMVar_hsa_circ_91710,RMVar_hsa_circ_260345,RMVar_hsa_circ_123470,RMVar_hsa_circ_260346 107544 RMVar_ID_107544 Human_SNP_ID_416506023 m1A Human chr9 + 130636023 130636023 130636023 TCAACCAGGTCACGCCGCCAGCGCTGCTCCTCAGGCCAGCTCCCCACCGGACTACACAATGGCCT TCAACCAGGTCACGCCGCCAGCGCTGCTCCTCCGGCCAGCTCCCCACCGGACTACACAATGGCCT A C FUBP3 Ensembl:ENSG00000107164 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:130634651..130636076;chr9:130632201..130636150 26863196 MeRIP-seq:(Medium) rs376352946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407657,Human_RBP_ID_22690415,Human_RBP_ID_22748239 Human_Splice_Rec_1091058,Human_Splice_Rec_1091098,Human_Splice_Rec_1091124 Human_miRNA_ID_2367019,Human_miRNA_ID_2725634,Human_miRNA_ID_3014822 RMVar_hsa_circ_87967,RMVar_hsa_circ_104170,RMVar_hsa_circ_260335,RMVar_hsa_circ_260337,RMVar_hsa_circ_115078,RMVar_hsa_circ_260344,RMVar_hsa_circ_120595,RMVar_hsa_circ_260343,RMVar_hsa_circ_91710,RMVar_hsa_circ_260345,RMVar_hsa_circ_123470,RMVar_hsa_circ_260346 107545 RMVar_ID_107545 Human_SNP_ID_416506038 m1A Human chr9 - 130636050 130636050 130636050 CGACCTGCTGTCTGTAATATTCTGCCCAGGCCATTGTGTAGTCCGGTGGGGAGCTGGCCTGAGGA CGACCTGCTGTCTGTAATATTCTGCCCAGGCCTTTGTGTAGTCCGGTGGGGAGCTGGCCTGAGGA T A RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130635957..130636150 26863196 MeRIP-seq:(Medium) rs1231465485 Functional Loss SNV dbSNP153 33..33 33 - - - 107546 RMVar_ID_107546 Human_SNP_ID_416519349 m1A Human chr9 + 130681658 130681658 130681658 CCGCCGCCGCCGCCGCGCACCACCTGCCGGCCATGGTGCTGTGAGCGCGCCCGCGCCCCCGCCGG CCGCCGCCGCCGCCGCGCACCACCTGCCGGCCGTGGTGCTGTGAGCGCGCCCGCGCCCCCGCCGG A G PRDM12 Ensembl:ENSG00000130711 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130681607..130681677 26863196 MeRIP-seq:(Medium) rs1344661944 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_691 107547 RMVar_ID_107547 Human_SNP_ID_416519363 m1A Human chr9 + 130681717 130681717 130681717 CGCCGGGCCCCGCGCGCTCCTGGGTCCCCGGCACCCCGGCCCCGCAGCGCGACTCGCCCTCCAGC CGCCGGGCCCCGCGCGCTCCTGGGTCCCCGGCCCCCCGGCCCCGCAGCGCGACTCGCCCTCCAGC A C PRDM12 Ensembl:ENSG00000130711 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130681667..130681790 26863196 MeRIP-seq:(Medium) rs920703936 Functional Loss SNV dbSNP153 33..33 33 - - - 107548 RMVar_ID_107548 Human_SNP_ID_416519364 m1A Human chr9 + 130681717 130681717 130681717 CGCCGGGCCCCGCGCGCTCCTGGGTCCCCGGCACCCCGGCCCCGCAGCGCGACTCGCCCTCCAGC CGCCGGGCCCCGCGCGCTCCTGGGTCCCCGGCTCCCCGGCCCCGCAGCGCGACTCGCCCTCCAGC A T PRDM12 Ensembl:ENSG00000130711 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130681667..130681790 26863196 MeRIP-seq:(Medium) rs920703936 Functional Loss SNV dbSNP153 33..33 33 - - - 107549 RMVar_ID_107549 Human_SNP_ID_416522373 m1A Human chr9 + 130693826 130693824 130693827 GGCGATGGAGATGAGGCTTCCAGTGGCTCGCAAGCCTCTTAGCGAGAGACTGGGCCGCGACACTA GGCGATGGAGATGAGGCTTCCAGTGGCTCGC___CCTCTTAGCGAGAGACTGGGCCGCGACACTA CAAG C EXOSC2 Ensembl:ENSG00000130713 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:130693776..130693967;chr9:130693776..130693875 26863196 MeRIP-seq:(Medium) rs1298632867 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5036515,Human_RBP_ID_18427236,Human_RBP_ID_26833666,Human_RBP_ID_27832852 Human_Splice_Rec_1091137,Human_Splice_Rec_1091147,Human_Splice_Rec_1091161,Human_Splice_Rec_1091175,Human_Splice_Rec_1091179,Human_Splice_Rec_1091195,Human_Splice_Rec_1091211,Human_Splice_Rec_1091225,Human_Splice_Rec_1091237,Human_Splice_Rec_1091245 107550 RMVar_ID_107550 Human_SNP_ID_416525026 m1A Human chr9 + 130704410 130704410 130704410 AAAATTAGCCAGGTGTGGTGGTGTGCACCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGTGTGGTGGTGTGCACCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA A G EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1002068791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 107551 RMVar_ID_107551 Human_SNP_ID_416525034 m1A Human chr9 + 130704446 130704446 130704446 CCAGCTATTTGGGAGGCTGAGGTGGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC CCAGCTATTTGGGAGGCTGAGGTGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC A G EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1139032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5014500 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 107552 RMVar_ID_107552 Human_SNP_ID_416527591 m1A Human chr9 + 130713144 130713144 130713144 GGTCCTGCGGCTGAGGAGCCCCTCCGCTGTCCACGGCCCCTACCGGCGGGGGGCGGCTGGGTCCC GGTCCTGCGGCTGAGGAGCCCCTCCGCTGTCCGCGGCCCCTACCGGCGGGGGGCGGCTGGGTCCC A G ABL1 Ensembl:ENSG00000097007 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130713093..130713244 26863196 MeRIP-seq:(Medium) rs1036598068 Functional Loss SNV dbSNP153 33..33 33 - - - 107553 RMVar_ID_107553 Human_SNP_ID_416552392 m1A Human chr9 + 130809417 130809413 130809418 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGA_____TGTGTGTGTGTGTGTGTGTGTGTGTGCACGT AGAGAG A ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130809393..130809490 26863196 MeRIP-seq:(Medium) rs1564296557 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_9352029,Human_RBP_ID_24289379 RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 107554 RMVar_ID_107554 Human_SNP_ID_416552408 m1A Human chr9 + 130809417 130809417 130809417 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT A T ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130809393..130809490 26863196 MeRIP-seq:(Medium) rs2855185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9352029,Human_RBP_ID_24289379 RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 107555 RMVar_ID_107555 Human_SNP_ID_416558545 m1A Human chr9 + 130835329 130835329 130835329 ATGGGCGGGCGCGGGCGCGCGGGGCGGCGGTGAGGGCGGCTGGCGGGGCCGGGGGCGCCGGGGGG ATGGGCGGGCGCGGGCGCGCGGGGCGGCGGTGGGGGCGGCTGGCGGGGCCGGGGGCGCCGGGGGG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr9:130835280..130835467;chr9:130835284..130835432 26863196 MeRIP-seq:(Medium) rs1328979388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3906426,Human_RBP_ID_5035937,Human_RBP_ID_8223462,Human_RBP_ID_9354967,Human_RBP_ID_18427409,Human_RBP_ID_21759478,Human_RBP_ID_26796604 RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 107556 RMVar_ID_107556 Human_SNP_ID_416558599 m1A Human chr9 - 130835383 130835383 130835383 CCCTCTCCCAGCTCGGTCCGCGGGCCCGGCTCAGGCCCGGCTCGGCCCGCGCGCCCCCCCGGCGC CCCTCTCCCAGCTCGGTCCGCGGGCCCGGCTCGGGCCCGGCTCGGCCCGCGCGCCCCCCCGGCGC T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130835346..130835472 26863196 MeRIP-seq:(Medium) rs1186260158 Functional Loss SNV dbSNP153 33..33 33 - - - 107557 RMVar_ID_107557 Human_SNP_ID_416558620 m1A Human chr9 - 130835406 130835406 130835406 GCCAGCACGTCGGGGGCCGGAACCCCTCTCCCAGCTCGGTCCGCGGGCCCGGCTCAGGCCCGGCT GCCAGCACGTCGGGGGCCGGAACCCCTCTCCCGGCTCGGTCCGCGGGCCCGGCTCAGGCCCGGCT T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130835355..130835455 26863196 MeRIP-seq:(Medium) rs765994887 Functional Loss SNV dbSNP153 33..33 33 - - - 107558 RMVar_ID_107558 Human_SNP_ID_416560447 m1A Human chr9 - 130841877 130841877 130841877 CTTCCCTATCACCAGTACTCAACACACGCAATATAACAAAAATATTTATGGTGTAACATGGTAAA CTTCCCTATCACCAGTACTCAACACACGCAATGTAACAAAAATATTTATGGTGTAACATGGTAAA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130841874..130842230 26863196 MeRIP-seq:(Medium) rs1011505518 Functional Loss SNV dbSNP153 33..33 33 - - - 107559 RMVar_ID_107559 Human_SNP_ID_416561007 m1A Human chr9 + 130844202 130844202 130844202 GAGTGACCTGGTCAGGTCTGCATTTGAGAAAGATGGCCCTGATAGTAGGGAGTGGAGGTGGAATG GAGTGACCTGGTCAGGTCTGCATTTGAGAAAGGTGGCCCTGATAGTAGGGAGTGGAGGTGGAATG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130844196..130844323 26863196 MeRIP-seq:(Medium) rs558410765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 107560 RMVar_ID_107560 Human_SNP_ID_416563252 m1A Human chr9 - 130852938 130852936 130852938 GGACTTACTTCACAAGACAAGGCTATTAACACACCCCACCCGTCCTTCCAGCTTTCTTGCCCCCA GGACTTACTTCACAAGACAAGGCTATTAACAC__CCCACCCGTCCTTCCAGCTTTCTTGCCCCCA GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130852931..130853069 26863196 MeRIP-seq:(Medium) rs10562700 Functional Loss DEL dbSNP153 33..34 33 - - - 107561 RMVar_ID_107561 Human_SNP_ID_416565941 m1A Human chr9 + 130862977 130862977 130862977 GAAGCACAAGCTGGGCGGGGGCCAGTACGGGGAGGTGTACGAGGGCGTGTGGAAGAAATACAGCC GAAGCACAAGCTGGGCGGGGGCCAGTACGGGGTGGTGTACGAGGGCGTGTGGAAGAAATACAGCC A T ABL1 Ensembl:ENSG00000097007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130862867..130862988 26863196 MeRIP-seq:(Medium) rs121913449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8930247,Human_RBP_ID_9315258,Human_RBP_ID_18131045,Human_RBP_ID_22733076,Human_RBP_ID_27574802 Human_Splice_Rec_1091267,Human_Splice_Rec_1091289 Human_miRNA_ID_2015881 Clinvar_Rec_692 RMVar_hsa_circ_52622,RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_296068,RMVar_hsa_circ_329890,RMVar_hsa_circ_260351,RMVar_hsa_circ_371059,RMVar_hsa_circ_286405,RMVar_hsa_circ_260355,RMVar_hsa_circ_260356,RMVar_hsa_circ_260357,RMVar_hsa_circ_260354,RMVar_hsa_circ_260359,RMVar_hsa_circ_260361,RMVar_hsa_circ_304389,RMVar_hsa_circ_347830,RMVar_hsa_circ_372061,RMVar_hsa_circ_109474,RMVar_hsa_circ_260360,RMVar_hsa_circ_260358 107562 RMVar_ID_107562 Human_SNP_ID_416568961 m1A Human chr9 - 130874922 130874922 130874922 TCCCCTGTCATCAACCTGCTCAGGCCAAAATCAGCTACCTTCACCAAGTGGTTCTCCCCTACCAG TCCCCTGTCATCAACCTGCTCAGGCCAAAATCGGCTACCTTCACCAAGTGGTTCTCCCCTACCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130874830..130874990 26863196 MeRIP-seq:(Medium) rs753439268 Functional Loss SNV dbSNP153 33..33 33 - - - 107563 RMVar_ID_107563 Human_SNP_ID_416568962 m1A Human chr9 - 130874922 130874922 130874922 TCCCCTGTCATCAACCTGCTCAGGCCAAAATCAGCTACCTTCACCAAGTGGTTCTCCCCTACCAG TCCCCTGTCATCAACCTGCTCAGGCCAAAATCCGCTACCTTCACCAAGTGGTTCTCCCCTACCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130874830..130874990 26863196 MeRIP-seq:(Medium) rs753439268 Functional Loss SNV dbSNP153 33..33 33 - - - 107564 RMVar_ID_107564 Human_SNP_ID_416571567 m1A Human chr9 + 130884032 130884032 130884032 ATTGCTCCCTCGAAAAGAGCGAGGTCCCCCGGAGGGCGGCCTGAATGAAGATGAGCGCCTTCTCC ATTGCTCCCTCGAAAAGAGCGAGGTCCCCCGGGGGGCGGCCTGAATGAAGATGAGCGCCTTCTCC A G ABL1 Ensembl:ENSG00000097007 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130883981..130884193 26863196 MeRIP-seq:(Medium) rs1467808878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8930262,Human_RBP_ID_9315716,Human_RBP_ID_22118959 Human_Splice_Rec_1091280,Human_Splice_Rec_1091302 RMVar_hsa_circ_260352,RMVar_hsa_circ_76537,RMVar_hsa_circ_109474,RMVar_hsa_circ_260358,RMVar_hsa_circ_88938,RMVar_hsa_circ_260363,RMVar_hsa_circ_104714,RMVar_hsa_circ_260365 107565 RMVar_ID_107565 Human_SNP_ID_416572102 m1A Human chr9 + 130885148 130885148 130885148 CAGTGACGCTGCCAAGCCCAGCCAGCCGGGAGAGGGCCTCAAAAAGCCCGTGCTCCCGGCCACTC CAGTGACGCTGCCAAGCCCAGCCAGCCGGGAGGGGGCCTCAAAAAGCCCGTGCTCCCGGCCACTC A G ABL1 Ensembl:ENSG00000097007 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:130885101..130885200 32194978 MeRIP-seq:(Medium) rs757466697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_76537,RMVar_hsa_circ_109474,RMVar_hsa_circ_260358,RMVar_hsa_circ_88938,RMVar_hsa_circ_260363,RMVar_hsa_circ_104714,RMVar_hsa_circ_260365 107566 RMVar_ID_107566 Human_SNP_ID_416572772 m1A Human chr9 - 130887082 130887082 130887082 TGCTCTCGGAGTTAGCTGCTCTGTCAAGGTCCAGGAGACCCCGGGTCCCTGCCCAGAGTCACAGC TGCTCTCGGAGTTAGCTGCTCTGTCAAGGTCCGGGAGACCCCGGGTCCCTGCCCAGAGTCACAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:130887001..130887300 32194978 MeRIP-seq:(Medium) rs1324221843 Functional Loss SNV dbSNP153 33..33 33 - - - 107567 RMVar_ID_107567 Human_SNP_ID_416577821 m1A Human chr9 + 130903640 130903640 130903640 AGACCTGACCTCAGAGAGACCTGACGTTCCCCACGATCTGCTAGGAGGACTCCAGGGGTGCTGTC AGACCTGACCTCAGAGAGACCTGACGTTCCCCGCGATCTGCTAGGAGGACTCCAGGGGTGCTGTC A G RF00017-4630 RNACentral:URS000096585E SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130903589..130903660 26863196 MeRIP-seq:(Medium) rs1489154230 Functional Loss SNV dbSNP153 33..33 33 - - - 107568 RMVar_ID_107568 Human_SNP_ID_416588809 m1A Human chr9 + 130939094 130939094 130939094 TAGGGAAAGGAGGCCGAACTGGCCCCCAGATAACGCGGCCGGCCGGAGGGCAGCAAACAGCCGCG TAGGGAAAGGAGGCCGAACTGGCCCCCAGATACCGCGGCCGGCCGGAGGGCAGCAAACAGCCGCG A C AL161733.1 Ensembl:ENSG00000236658 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130939086..130939192 26863196 MeRIP-seq:(Medium) rs548978672 Functional Loss SNV dbSNP153 33..33 33 - - - 107569 RMVar_ID_107569 Human_SNP_ID_416594314 m1A Human chr9 - 130958685 130958661 130958685 GTGATGGCGGTGGTGGTGGTGATGGTGATGACAGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT GTGATGGCGGTGGTGGTGGTGATGGTGATGAC________________________GGTGGTGGT CACCATCACCACCATCACCACCACT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130958624..130958723 26863196 MeRIP-seq:(Medium) rs1282918399 Functional Loss DEL dbSNP153 33..56 33 - - - 107570 RMVar_ID_107570 Human_SNP_ID_416594343 m1A Human chr9 + 130958698 130958675 130958699 TCACCACCATCACCACCACTGTCATCACCATCACCACCACCACCGCCATCACCACCACCACCACC TCACCACCAT________________________CACCACCACCGCCATCACCACCACCACCACC TCACCACCACTGTCATCACCATCAC T RF00017-4630 RNACentral:URS000096585E SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130958657..130958744 26863196 MeRIP-seq:(Medium) rs1564347652 Functional Loss DEL dbSNP153 11..34 33 - - - 107571 RMVar_ID_107571 Human_SNP_ID_416594348 m1A Human chr9 - 130958685 130958679 130958685 GTGATGGCGGTGGTGGTGGTGATGGTGATGACAGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT GTGATGGCGGTGGTGGTGGTGATGGTGATGAC______GGTGATGGTGGTGATGGTGGTGGTGGT CACCACT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130958624..130958723 26863196 MeRIP-seq:(Medium) rs1246812096 Functional Loss DEL dbSNP153 33..38 33 - - - 107572 RMVar_ID_107572 Human_SNP_ID_416594349 m1A Human chr9 - 130958685 130958682 130958685 GTGATGGCGGTGGTGGTGGTGATGGTGATGACAGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT GTGATGGCGGTGGTGGTGGTGATGGTGATGAC___GGTGGTGATGGTGGTGATGGTGGTGGTGGT CACT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130958624..130958723 26863196 MeRIP-seq:(Medium) rs1447585357 Functional Loss DEL dbSNP153 33..35 33 - - - 107573 RMVar_ID_107573 Human_SNP_ID_416594355 m1A Human chr9 - 130958685 130958685 130958685 GTGATGGCGGTGGTGGTGGTGATGGTGATGACAGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT GTGATGGCGGTGGTGGTGGTGATGGTGATGACGGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130958624..130958723 26863196 MeRIP-seq:(Medium) rs1025790514 Functional Loss SNV dbSNP153 33..33 33 - - - 107574 RMVar_ID_107574 Human_SNP_ID_416594368 m1A Human chr9 + 130958698 130958696 130958699 TCACCACCATCACCACCACTGTCATCACCATCACCACCACCACCGCCATCACCACCACCACCACC TCACCACCATCACCACCACTGTCATCACCAT___CACCACCACCGCCATCACCACCACCACCACC TCAC T RF00017-4630 RNACentral:URS000096585E SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130958657..130958744 26863196 MeRIP-seq:(Medium) rs1315493644 Functional Loss DEL dbSNP153 32..34 33 - - - 107575 RMVar_ID_107575 Human_SNP_ID_416608939 m1A Human chr9 + 131009474 131009474 131009474 CTGCGACGCCGCCGACCCCCAGCGCCACCACAACGCCTCCTACCTCACCGACTTCCACAGCCAGG CTGCGACGCCGCCGACCCCCAGCGCCACCACAGCGCCTCCTACCTCACCGACTTCCACAGCCAGG A G LAMC3 Ensembl:ENSG00000050555 Protein coding exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr9:131009427..131009559;chr9:131009193..131009517 26863196 MeRIP-seq:(Medium) rs757872953 Functional Loss SNV dbSNP153 33..33 33 - - - 107576 RMVar_ID_107576 Human_SNP_ID_416615509 m1A Human chr9 + 131033441 131033441 131033441 CTGGGGTCGGGGAGGACAGGAGCTGGTGCTGCAGATGGGACCCAAGAGTGGGAAGGCTGGGGTTG CTGGGGTCGGGGAGGACAGGAGCTGGTGCTGCCGATGGGACCCAAGAGTGGGAAGGCTGGGGTTG A C LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:131033325..131033596 26863196 MeRIP-seq:(Medium) rs891369136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88082,RMVar_hsa_circ_260367 107577 RMVar_ID_107577 Human_SNP_ID_416621302 m1A Human chr9 + 131052926 131052926 131052926 TCCACTTCCAGCGGCTCCTCGCCAACCTGACCAGCCTCCGCCTCCGCGTCAGTCCCGGCCCCAGC TCCACTTCCAGCGGCTCCTCGCCAACCTGACCGGCCTCCGCCTCCGCGTCAGTCCCGGCCCCAGC A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131052861..131052975 26863196 MeRIP-seq:(Medium) rs1564377303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1091408,Human_Splice_Rec_1091409 107578 RMVar_ID_107578 Human_SNP_ID_416622534 m1A Human chr9 - 131056977 131056977 131056977 AACAAATCTCCACCCAGGAGGCTGGCGGGGAAAGCCCTGGCCGGGCGGATGTGAGCCGGACCTCA AACAAATCTCCACCCAGGAGGCTGGCGGGGAAGGCCCTGGCCGGGCGGATGTGAGCCGGACCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131056926..131057072 26863196 MeRIP-seq:(Medium) rs1341046086 Functional Loss SNV dbSNP153 33..33 33 - - - 107579 RMVar_ID_107579 Human_SNP_ID_416626867 m1A Human chr9 + 131071531 131071531 131071531 GCCAGACTGACTTTGACGGAGGGGTGGCTCCAAGGGTCCGACTGTGGCAGTCCCTGGGGACCACT GCCAGACTGACTTTGACGGAGGGGTGGCTCCAGGGGTCCGACTGTGGCAGTCCCTGGGGACCACT A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131071448..131071569 26863196 MeRIP-seq:(Medium) rs566482956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1091422,Human_Splice_Rec_1091423 107580 RMVar_ID_107580 Human_SNP_ID_416627434 m1A Human chr9 + 131073317 131073317 131073317 GCCACCTGGCCACAGAGGCCCGTGCCCTCGCCAGGAGGTGAGTCCCAAGACATGGTGAGCTTACA GCCACCTGGCCACAGAGGCCCGTGCCCTCGCCGGGAGGTGAGTCCCAAGACATGGTGAGCTTACA A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131073226..131073325 26863196 MeRIP-seq:(Medium) rs750966093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1091426,Human_Splice_Rec_1091427 107581 RMVar_ID_107581 Human_SNP_ID_416628055 m1A Human chr9 - 131075799 131075799 131075799 GCTGTGTGAGGACACCCACCTGAGCATTACCAAGGGCTCGCAGGGAAGGGGCCCAGGATCAGAAC GCTGTGTGAGGACACCCACCTGAGCATTACCAGGGGCTCGCAGGGAAGGGGCCCAGGATCAGAAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131075795..131075950 26863196 MeRIP-seq:(Medium) rs754244303 Functional Loss SNV dbSNP153 33..33 33 - - - 107582 RMVar_ID_107582 Human_SNP_ID_416629129 m1A Human chr9 + 131079188 131079188 131079188 AGTCCCGGGCTGAAGACCTGGGCCTGAAGGCGAAGGCCCTGGAGAAGACAGTTGCATCATGGCAG AGTCCCGGGCTGAAGACCTGGGCCTGAAGGCGGAGGCCCTGGAGAAGACAGTTGCATCATGGCAG A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:131079184..131079271 26863410 MeRIP-seq:(Medium) rs1032071333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1091432 RMVar_hsa_circ_6532 107583 RMVar_ID_107583 Human_SNP_ID_416630008 m1A Human chr9 + 131082137 131082137 131082137 TCCAGGCTGCGACAGTGACTGTCATGGGAGCCAGGACTCTGCTGGCTGATCTGGAAGGTACGTGA TCCAGGCTGCGACAGTGACTGTCATGGGAGCCGGGACTCTGCTGGCTGATCTGGAAGGTACGTGA A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131082022..131082187 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1091434,Human_Splice_Rec_1091435,Human_Splice_Rec_1091444,Human_Splice_Rec_1091445 RMVar_hsa_circ_6532 107584 RMVar_ID_107584 Human_SNP_ID_416631421 m1A Human chr9 + 131087527 131087527 131087527 GGGAGCGGAAACAGGCGCACCGCCGTGCCAGCAGGCTCACCAGCCAGACGCAAGCCACGCTCCAA GGGAGCGGAAACAGGCGCACCGCCGTGCCAGCGGGCTCACCAGCCAGACGCAAGCCACGCTCCAA A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131087430..131087621 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1091438,Human_Splice_Rec_1091439,Human_Splice_Rec_1091448,Human_Splice_Rec_1091449,Human_Splice_Rec_1091454,Human_Splice_Rec_1091455 RMVar_hsa_circ_6532,RMVar_hsa_circ_36361 107585 RMVar_ID_107585 Human_SNP_ID_416632574 m1A Human chr9 - 131091717 131091717 131091717 GAATGGCCTCCAGGTTCTGTTTGTCGGCGCGGATCTCGGCGAGGTCACTCTCGAAGCCCTGGATC GAATGGCCTCCAGGTTCTGTTTGTCGGCGCGGTTCTCGGCGAGGTCACTCTCGAAGCCCTGGATC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131091671..131091894 26863196 MeRIP-seq:(Medium) rs772095312 Functional Loss SNV dbSNP153 33..33 33 - - - 107586 RMVar_ID_107586 Human_SNP_ID_416632575 m1A Human chr9 - 131091717 131091717 131091717 GAATGGCCTCCAGGTTCTGTTTGTCGGCGCGGATCTCGGCGAGGTCACTCTCGAAGCCCTGGATC GAATGGCCTCCAGGTTCTGTTTGTCGGCGCGGCTCTCGGCGAGGTCACTCTCGAAGCCCTGGATC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131091671..131091894 26863196 MeRIP-seq:(Medium) rs772095312 Functional Loss SNV dbSNP153 33..33 33 - - - 107587 RMVar_ID_107587 Human_SNP_ID_416638380 m1A Human chr9 + 131113122 131113122 131113122 AGACTAAACAGAGAGCCGGGAAATACAAGGTTAGCAGACTGTGGTAGGTGCTTCAGTGAGAAATG AGACTAAACAGAGAGCCGGGAAATACAAGGTTGGCAGACTGTGGTAGGTGCTTCAGTGAGAAATG A G AIF1L Ensembl:ENSG00000126878 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131113121..131113191 26863196 MeRIP-seq:(Medium) rs1309398080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3594,RMVar_hsa_circ_49426 107588 RMVar_ID_107588 Human_SNP_ID_416641839 m1A Human chr9 + 131125690 131125690 131125690 GCCGTGGGAGGCAGCGTTGGCTGCTTCGACACACTGAGGGCGGCGCGATGGGAGACGAGATGGAT GCCGTGGGAGGCAGCGTTGGCTGCTTCGACACGCTGAGGGCGGCGCGATGGGAGACGAGATGGAT A G NUP214 Ensembl:ENSG00000126883 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:131125640..131125750;chr9:131125639..131125731 26863196 MeRIP-seq:(Medium) rs1360641404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256619,Human_RBP_ID_5014947,Human_RBP_ID_5329665,Human_RBP_ID_8930278,Human_RBP_ID_9315279,Human_RBP_ID_19025871,Human_RBP_ID_22837875,Human_RBP_ID_27843661 Human_Splice_Rec_1091541,Human_Splice_Rec_1091611,Human_Splice_Rec_1091681,Human_Splice_Rec_1091751 RMVar_hsa_circ_267288 107589 RMVar_ID_107589 Human_SNP_ID_416646904 m1A Human chr9 - 131144354 131144354 131144354 AATGGGAGCAGCAGGTGATGAAGGTGGCAGAGAGGCAGGGGCTGCAGCTGCAGAAGCATCCAGTT AATGGGAGCAGCAGGTGATGAAGGTGGCAGAGGGGCAGGGGCTGCAGCTGCAGAAGCATCCAGTT T C AL157938.2 Ensembl:ENSG00000236986 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131144308..131144425 26863196 MeRIP-seq:(Medium) rs781271894 Functional Loss SNV dbSNP153 33..33 33 - - - 107590 RMVar_ID_107590 Human_SNP_ID_416646950 m1A Human chr9 + 131144465 131144465 131144465 CCTTTGGTTCTTCATCTTTGAAGTCATCTGCTACGGTCACTGGGGAGCCCCCTTCATATTCCAGT CCTTTGGTTCTTCATCTTTGAAGTCATCTGCTGCGGTCACTGGGGAGCCCCCTTCATATTCCAGT A G NUP214 Ensembl:ENSG00000126883 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:131144426..131144475 26863196 MeRIP-seq:(Medium) rs746775178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90820,Human_RBP_ID_3976018,Human_RBP_ID_5410195,Human_RBP_ID_5535509,Human_RBP_ID_16596782,Human_RBP_ID_17321440,Human_RBP_ID_17435719,Human_RBP_ID_21694445,Human_RBP_ID_22119433,Human_RBP_ID_26239917 Human_miRNA_ID_2257338 RMVar_hsa_circ_4083,RMVar_hsa_circ_11119,RMVar_hsa_circ_267288,RMVar_hsa_circ_21917,RMVar_hsa_circ_74456,RMVar_hsa_circ_123399,RMVar_hsa_circ_114019,RMVar_hsa_circ_51457,RMVar_hsa_circ_260373,RMVar_hsa_circ_260374,RMVar_hsa_circ_121183,RMVar_hsa_circ_124469,RMVar_hsa_circ_25200,RMVar_hsa_circ_83409,RMVar_hsa_circ_260376,RMVar_hsa_circ_260377,RMVar_hsa_circ_114782,RMVar_hsa_circ_260379,RMVar_hsa_circ_41899,RMVar_hsa_circ_328871,RMVar_hsa_circ_328855,RMVar_hsa_circ_39622,RMVar_hsa_circ_75185,RMVar_hsa_circ_260381,RMVar_hsa_circ_260380,RMVar_hsa_circ_260383,RMVar_hsa_circ_57087,RMVar_hsa_circ_91592,RMVar_hsa_circ_122118,RMVar_hsa_circ_260384,RMVar_hsa_circ_269295,RMVar_hsa_circ_303641,RMVar_hsa_circ_318669,RMVar_hsa_circ_116415,RMVar_hsa_circ_260385,RMVar_hsa_circ_260386 107591 RMVar_ID_107591 Human_SNP_ID_416647003 m1A Human chr9 + 131144575 131144575 131144575 TTCTCTTTTGTTCCCCCTTCTAAAGCCTCCCTAGCCCCCACCCCTGCAGCGTCTCCTGTGGCTCC TTCTCTTTTGTTCCCCCTTCTAAAGCCTCCCTGGCCCCCACCCCTGCAGCGTCTCCTGTGGCTCC A G NUP214 Ensembl:ENSG00000126883 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:131144528..131144658 26863196 MeRIP-seq:(Medium) rs754995317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90821,Human_RBP_ID_797325,Human_RBP_ID_5135320,Human_RBP_ID_17094969,Human_RBP_ID_17437375,Human_RBP_ID_18962385,Human_RBP_ID_24563755,Human_RBP_ID_26239918 Human_Splice_Rec_1091870 Human_miRNA_ID_2029274,Human_miRNA_ID_2689785,Human_miRNA_ID_2693023 RMVar_hsa_circ_4083,RMVar_hsa_circ_11119,RMVar_hsa_circ_267288,RMVar_hsa_circ_21917,RMVar_hsa_circ_74456,RMVar_hsa_circ_123399,RMVar_hsa_circ_114019,RMVar_hsa_circ_51457,RMVar_hsa_circ_260373,RMVar_hsa_circ_260374,RMVar_hsa_circ_121183,RMVar_hsa_circ_124469,RMVar_hsa_circ_25200,RMVar_hsa_circ_83409,RMVar_hsa_circ_260376,RMVar_hsa_circ_260377,RMVar_hsa_circ_114782,RMVar_hsa_circ_260379,RMVar_hsa_circ_41899,RMVar_hsa_circ_328871,RMVar_hsa_circ_328855,RMVar_hsa_circ_39622,RMVar_hsa_circ_75185,RMVar_hsa_circ_260381,RMVar_hsa_circ_260380,RMVar_hsa_circ_260383,RMVar_hsa_circ_57087,RMVar_hsa_circ_91592,RMVar_hsa_circ_122118,RMVar_hsa_circ_260384,RMVar_hsa_circ_269295,RMVar_hsa_circ_303641,RMVar_hsa_circ_318669,RMVar_hsa_circ_116415,RMVar_hsa_circ_260385,RMVar_hsa_circ_260386 107592 RMVar_ID_107592 Human_SNP_ID_416647476 m1A Human chr9 - 131146222 131146222 131146222 GCTGAGAGAGGTGTGGGGTGGCTGAGTGGTCCAGAAGCAGCTGGCTTGGAGGCAGAAGAGAATGG GCTGAGAGAGGTGTGGGGTGGCTGAGTGGTCCGGAAGCAGCTGGCTTGGAGGCAGAAGAGAATGG T C AL157938.2 Ensembl:ENSG00000236986 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:131146067..131146275 26863196 MeRIP-seq:(Medium) rs1472993945 Functional Loss SNV dbSNP153 33..33 33 - - - 107593 RMVar_ID_107593 Human_SNP_ID_416647494 m1A Human chr9 - 131146261 131146261 131146261 GGCAAGACTGAGGACTTCAATGGCACGGAACTAGGTGGTGCTGAGAGAGGTGTGGGGTGGCTGAG GGCAAGACTGAGGACTTCAATGGCACGGAACTTGGTGGTGCTGAGAGAGGTGTGGGGTGGCTGAG T A AL157938.2 Ensembl:ENSG00000236986 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131146115..131146304 26863196 MeRIP-seq:(Medium) rs1319249528 Functional Loss SNV dbSNP153 33..33 33 - - - 107594 RMVar_ID_107594 Human_SNP_ID_416677271 m1A Human chr9 - 131259924 131259924 131259924 AGCCTTAACTTCCCTTGGGCGGCTCTAGGAGGAGAGAGGCAGGCTCCTGTGAGCCCAGGGAATTT AGCCTTAACTTCCCTTGGGCGGCTCTAGGAGGGGAGAGGCAGGCTCCTGTGAGCCCAGGGAATTT T C FAM78A Ensembl:ENSG00000126882 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:131259874..131260025 32194978 MeRIP-seq:(Medium) rs1330156567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224691,Human_RBP_ID_18196985,Human_RBP_ID_26565469 RMVar_hsa_circ_90776,RMVar_hsa_circ_101181,RMVar_hsa_circ_93551,RMVar_hsa_circ_260419,RMVar_hsa_circ_260420,RMVar_hsa_circ_260421 107595 RMVar_ID_107595 Human_SNP_ID_416677706 m1A Human chr9 - 131261324 131261324 131261324 CCTCAGGTCCAGCTGGGAGCTCCCCGACCTCCAGGAGGGCAAGATCCAAGCCATCAGCGACTCGG CCTCAGGTCCAGCTGGGAGCTCCCCGACCTCCGGGAGGGCAAGATCCAAGCCATCAGCGACTCGG T C FAM78A Ensembl:ENSG00000126882 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:131261274..131262715 32194978 MeRIP-seq:(Medium) rs772008228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22690443 Human_Splice_Rec_1092100,Human_Splice_Rec_1092106,Human_Splice_Rec_1092108,Human_Splice_Rec_1092114 RMVar_hsa_circ_90776,RMVar_hsa_circ_101181,RMVar_hsa_circ_93551,RMVar_hsa_circ_260419,RMVar_hsa_circ_260420,RMVar_hsa_circ_260421 107596 RMVar_ID_107596 Human_SNP_ID_416680262 m1A Human chr9 - 131270514 131270514 131270514 AGAGCTCCCCCAGGACCAGCCCTGGCCAAGGGATTGCTGCAGCCCTCATCCACCTTCCAAGCACT AGAGCTCCCCCAGGACCAGCCCTGGCCAAGGGCTTGCTGCAGCCCTCATCCACCTTCCAAGCACT T G FAM78A Ensembl:ENSG00000126882 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:131270513..131275947 32194978 MeRIP-seq:(Medium) rs924789846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1092109 RMVar_hsa_circ_101181,RMVar_hsa_circ_260421 107597 RMVar_ID_107597 Human_SNP_ID_416681797 m1A Human chr9 - 131276598 131276598 131276598 CCGGAGGGAGCGCGTGCGGAAGGCCGGAGGGCAGGAAGTCAGGCTTCTGCCGCGAGGGTGGCGCG CCGGAGGGAGCGCGTGCGGAAGGCCGGAGGGCGGGAAGTCAGGCTTCTGCCGCGAGGGTGGCGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131276461..131276937 26863196 MeRIP-seq:(Medium) rs1407613963 Functional Loss SNV dbSNP153 33..33 33 - - - 107598 RMVar_ID_107598 Human_SNP_ID_416681812 m1A Human chr9 + 131276638 131276632 131276638 GGCCTTCCGCACGCGCTCCCTCCGGGCCCCGCACCCGCACCCGCCCGGCGCGGTCGAATCAATTG GGCCTTCCGCACGCGCTCCCTCCGGGC______CCCGCACCCGCCCGGCGCGGTCGAATCAATTG CCCCGCA C RF00017-1792 RNACentral:URS000096ECA5 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:131276506..131276709 26863196 MeRIP-seq:(Medium) rs908559050 Functional Loss DEL dbSNP153 28..33 33 - - - 107599 RMVar_ID_107599 Human_SNP_ID_416682094 m1A Human chr9 - 131277587 131277587 131277587 AACGTGCCCGCGGCCGGGTCAGGGGCGTCCGGAGAGCGGCTGCCCGGGCCAGCGGAGTGGCCCCC AACGTGCCCGCGGCCGGGTCAGGGGCGTCCGGGGAGCGGCTGCCCGGGCCAGCGGAGTGGCCCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:131277363..131277691 26863196 MeRIP-seq:(Medium) rs1156443410 Functional Loss SNV dbSNP153 33..33 33 - - - 107600 RMVar_ID_107600 Human_SNP_ID_416713956 m1A Human chr9 + 131394135 131394135 131394135 TCCACCGCGCAGCGACGAGCGAGCCCGGGAGGAGGGAGGGAGCGAGCGAGCGAGCAGCCCGCGCC TCCACCGCGCAGCGACGAGCGAGCCCGGGAGGGGGGAGGGAGCGAGCGAGCGAGCAGCCCGCGCC A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:131394076..131394292 26863196 MeRIP-seq:(Medium) rs1223962168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256629,Human_RBP_ID_5035939,Human_RBP_ID_5228126,Human_RBP_ID_5330102,Human_RBP_ID_9339132,Human_RBP_ID_18427238,Human_RBP_ID_23094671 107601 RMVar_ID_107601 Human_SNP_ID_416713984 m1A Human chr9 - 131394190 131394180 131394191 GTCGGGCGGCGGTCGGGCACGGGGGCGGCGGGATGGCGGCGGATTGCGAGGCGGCGGCGCGGGCT GTCGGGCGGCGGTCGGGCACGGGGGCGGCGG___________ATTGCGAGGCGGCGGCGCGGGCT TCCGCCGCCATC T RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:131394051..131394275 26863410 MeRIP-seq:(Medium) rs1225452222 Functional Loss DEL dbSNP153 32..42 33 - - - 107602 RMVar_ID_107602 Human_SNP_ID_416713992 m1A Human chr9 - 131394223 131394212 131394223 GTTCCGCGGGCGCGGCCGGGCCGGGCGATGGCAGTCGGGCGGCGGTCGGGCACGGGGGCGGCGGG GTTCCGCGGGCGCGGCCGGGCCGGGCGATGGC___________GGTCGGGCACGGGGGCGGCGGG CGCCGCCCGACT C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:131394053..131394236 26863410 MeRIP-seq:(Medium) rs1176462715 Functional Loss DEL dbSNP153 33..43 33 - - - 107603 RMVar_ID_107603 Human_SNP_ID_416713997 m1A Human chr9 - 131394223 131394223 131394223 GTTCCGCGGGCGCGGCCGGGCCGGGCGATGGCAGTCGGGCGGCGGTCGGGCACGGGGGCGGCGGG GTTCCGCGGGCGCGGCCGGGCCGGGCGATGGCTGTCGGGCGGCGGTCGGGCACGGGGGCGGCGGG T A RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr9:131394053..131394236 26863410 MeRIP-seq:(Medium) rs1244126270 Functional Loss SNV dbSNP153 33..33 33 - - - 107604 RMVar_ID_107604 Human_SNP_ID_416714114 m1A Human chr9 - 131394540 131394540 131394540 GGCGAGCCCTGAGGGAGTCGCGCGGCCCCTGGACCCCGCCCGAGCCTGAGGCCGCGCGGCGCCGC GGCGAGCCCTGAGGGAGTCGCGCGGCCCCTGGCCCCCGCCCGAGCCTGAGGCCGCGCGGCGCCGC T G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131394533..131394899 26863196 MeRIP-seq:(Medium) rs891304062 Functional Loss SNV dbSNP153 33..33 33 - - - 107605 RMVar_ID_107605 Human_SNP_ID_416714188 m1A Human chr9 + 131394720 131394720 131394720 CCCAATTGACGGAGCAGCGCGCCCGAGGCGGGATCCTGCGGGGTCGGGCCTTGGGTCCGGGGCGC CCCAATTGACGGAGCAGCGCGCCCGAGGCGGGGTCCTGCGGGGTCGGGCCTTGGGTCCGGGGCGC A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131394708..131394812 26863196 MeRIP-seq:(Medium) rs528879095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15558,Human_RBP_ID_8223467,Human_RBP_ID_18467883,Human_RBP_ID_26795969 RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 107606 RMVar_ID_107606 Human_SNP_ID_416717686 m1A Human chr9 - 131406089 131406089 131406089 CCTGCCTGCTCCAAACCCCCGGGCCCCCGGGGAGGGCTGAATCCAGGAACCATTAATAGCTGCGG CCTGCCTGCTCCAAACCCCCGGGCCCCCGGGGCGGGCTGAATCCAGGAACCATTAATAGCTGCGG T G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:131406084..131406222 32194978 MeRIP-seq:(Medium) rs1225724910 Functional Loss SNV dbSNP153 33..33 33 - - - 107607 RMVar_ID_107607 Human_SNP_ID_416724968 m1A Human chr9 - 131430062 131430062 131430062 TCTGCCTTTGAAATAGAGAAGAAAAAAAAAAAAAGAGAGAGAAAAAAAAAAAAGAGTGTCACTAC TCTGCCTTTGAAATAGAGAAGAAAAAAAAAAAGAGAGAGAGAAAAAAAAAAAAGAGTGTCACTAC T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131430056..131430200 26863196 MeRIP-seq:(Medium) rs76644652 Functional Loss SNV dbSNP153 33..33 33 - - - 107608 RMVar_ID_107608 Human_SNP_ID_416725971 m1A Human chr9 + 131432727 131432727 131432727 GCTTGAAGTCTGAAAACAAAGGAAACGACCCCAACATCGTGATAGTACCCAAGGACGGGACGGGA GCTTGAAGTCTGAAAACAAAGGAAACGACCCCCACATCGTGATAGTACCCAAGGACGGGACGGGA A C PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:131432676..131432800 26863196 MeRIP-seq:(Medium) rs1336095697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90907,Human_RBP_ID_963976,Human_RBP_ID_3976049,Human_RBP_ID_5154847,Human_RBP_ID_5633807,Human_RBP_ID_9407681,Human_RBP_ID_18131188,Human_RBP_ID_23090582,Human_RBP_ID_26360519,Human_RBP_ID_27574807 Human_Splice_Rec_1092135,Human_Splice_Rec_1092195,Human_Splice_Rec_1092207 RMVar_hsa_circ_3344,RMVar_hsa_circ_288268,RMVar_hsa_circ_113359,RMVar_hsa_circ_260425,RMVar_hsa_circ_347650,RMVar_hsa_circ_354707,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_353982,RMVar_hsa_circ_311348,RMVar_hsa_circ_271019,RMVar_hsa_circ_271797,RMVar_hsa_circ_280454,RMVar_hsa_circ_271433,RMVar_hsa_circ_56692,RMVar_hsa_circ_81143,RMVar_hsa_circ_30116,RMVar_hsa_circ_34553,RMVar_hsa_circ_260429,RMVar_hsa_circ_260431,RMVar_hsa_circ_260433,RMVar_hsa_circ_260434,RMVar_hsa_circ_260432,RMVar_hsa_circ_260430,RMVar_hsa_circ_313327,RMVar_hsa_circ_260427,RMVar_hsa_circ_260428,RMVar_hsa_circ_336355,RMVar_hsa_circ_260435,RMVar_hsa_circ_378224,RMVar_hsa_circ_335846,RMVar_hsa_circ_286050,RMVar_hsa_circ_286450,RMVar_hsa_circ_281372,RMVar_hsa_circ_260437,RMVar_hsa_circ_260439,RMVar_hsa_circ_260440,RMVar_hsa_circ_260438,RMVar_hsa_circ_260436 107609 RMVar_ID_107609 Human_SNP_ID_416729773 m1A Human chr9 - 131446514 131446514 131446514 GGGGTCCTTAGAATCGCTGGTACATGCCGAGGAGGGGGCTCCATCTCCCGTACTCGAGTTCCTGC GGGGTCCTTAGAATCGCTGGTACATGCCGAGGTGGGGGCTCCATCTCCCGTACTCGAGTTCCTGC T A RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:131446465..131446538;chr9:131446464..131446551 26863196 MeRIP-seq:(Medium) rs1564286619 Functional Loss SNV dbSNP153 33..33 33 - - - 107610 RMVar_ID_107610 Human_SNP_ID_416732264 m1A Human chr9 + 131455151 131455151 131455151 TGATGATGAAGAGGAGGAAGAAGTTGTGAAGGACGGCAGGCCAAAGTGGTAAGGACCCGTTCCTG TGATGATGAAGAGGAGGAAGAAGTTGTGAAGGGCGGCAGGCCAAAGTGGTAAGGACCCGTTCCTG A G PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:131455126..131455150 26863196 MeRIP-seq:(Medium) rs772968626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_846585,Human_RBP_ID_961728,Human_RBP_ID_3976055,Human_RBP_ID_5015246,Human_RBP_ID_5227166,Human_RBP_ID_5637090,Human_RBP_ID_9315289,Human_RBP_ID_16601358,Human_RBP_ID_18472802,Human_RBP_ID_19025885,Human_RBP_ID_23090636,Human_RBP_ID_24289981,Human_RBP_ID_26362277 Human_Splice_Rec_1092148,Human_Splice_Rec_1092149,Human_Splice_Rec_1092220,Human_Splice_Rec_1092221,Human_Splice_Rec_1092269 RMVar_hsa_circ_3344,RMVar_hsa_circ_354707,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_311348,RMVar_hsa_circ_271433,RMVar_hsa_circ_56692,RMVar_hsa_circ_81143,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_260429,RMVar_hsa_circ_313327,RMVar_hsa_circ_260427,RMVar_hsa_circ_260428,RMVar_hsa_circ_335846,RMVar_hsa_circ_344873,RMVar_hsa_circ_260440,RMVar_hsa_circ_368739,RMVar_hsa_circ_260441,RMVar_hsa_circ_260442,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_340980,RMVar_hsa_circ_108160,RMVar_hsa_circ_260446,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_22227,RMVar_hsa_circ_287951,RMVar_hsa_circ_84564,RMVar_hsa_circ_260452,RMVar_hsa_circ_8531,RMVar_hsa_circ_94101,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_260458,RMVar_hsa_circ_76928,RMVar_hsa_circ_284131,RMVar_hsa_circ_350392,RMVar_hsa_circ_364155,RMVar_hsa_circ_373703,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_260465,RMVar_hsa_circ_70003,RMVar_hsa_circ_260464,RMVar_hsa_circ_260462 107611 RMVar_ID_107611 Human_SNP_ID_416733401 m1A Human chr9 - 131459154 131459153 131459154 GCCTCCTAGGGTCCCAACTGTTCCTAGGACAAACCACATTTGATGTTAAGTTTTTGCACTCAGGC GCCTCCTAGGGTCCCAACTGTTCCTAGGACAA_CCACATTTGATGTTAAGTTTTTGCACTCAGGC GT G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131459151..131459325 26863196 MeRIP-seq:(Medium) rs780641574 Functional Loss DEL dbSNP153 33..33 33 - - - 107612 RMVar_ID_107612 Human_SNP_ID_416735165 m1A Human chr9 + 131464975 131464975 131464975 CTCAAGCAGCTGGACCAGAAGTGTAAGCAGGCACGAAAGGCAGGTGAGGCCCGGAAGCAGGCAGA CTCAAGCAGCTGGACCAGAAGTGTAAGCAGGCGCGAAAGGCAGGTGAGGCCCGGAAGCAGGCAGA A G PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:131464808..131465122;chr9:131464776..131465050 26863196 MeRIP-seq:(Medium) rs757174918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90927,Human_RBP_ID_3975062,Human_RBP_ID_5535124,Human_RBP_ID_5633815,Human_RBP_ID_16601671,Human_RBP_ID_18141261,Human_RBP_ID_18196994,Human_RBP_ID_18472803,Human_RBP_ID_19024485,Human_RBP_ID_26361320 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_271433,RMVar_hsa_circ_56692,RMVar_hsa_circ_81143,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_260427,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_94101,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_260458,RMVar_hsa_circ_76928,RMVar_hsa_circ_350392,RMVar_hsa_circ_364155,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_64264,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_44625,RMVar_hsa_circ_260468 107613 RMVar_ID_107613 Human_SNP_ID_416736019 m1A Human chr9 + 131467734 131467732 131467735 TCAGAAGTCCCTTCCTCCCCGATTCCAGCGCCAGCAGCAGCAACAACAGCAGGTAAACAGATGAG TCAGAAGTCCCTTCCTCCCCGATTCCAGCGC___CAGCAGCAACAACAGCAGGTAAACAGATGAG CCAG C PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:131467726..131467750 26863196 MeRIP-seq:(Medium) rs1375113313 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_90928,Human_RBP_ID_797374,Human_RBP_ID_964623,Human_RBP_ID_1058274,Human_RBP_ID_3976060,Human_RBP_ID_5535125,Human_RBP_ID_7904695,Human_RBP_ID_9408746,Human_RBP_ID_26361322,Human_RBP_ID_27832877 Human_Splice_Rec_1092155,Human_Splice_Rec_1092227,Human_Splice_Rec_1092273 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_271433,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_364155,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_44625,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_46956,RMVar_hsa_circ_260469 107614 RMVar_ID_107614 Human_SNP_ID_416736837 m1A Human chr9 + 131470840 131470840 131470840 GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCACCCCCAGCGCACCTTTTACCCACACCACCCCC GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCCCCCCCAGCGCACCTTTTACCCACACCACCCCC A C PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131470764..131471003 26863196 MeRIP-seq:(Medium) rs1398997491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90929,Human_RBP_ID_713770 Human_Splice_Rec_1092156,Human_Splice_Rec_1092228,Human_Splice_Rec_1092274 Human_miRNA_ID_2143493,Human_miRNA_ID_2145024,Human_miRNA_ID_2684412,Human_miRNA_ID_2687529 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_11680,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_260469 107615 RMVar_ID_107615 Human_SNP_ID_416736838 m1A Human chr9 + 131470840 131470840 131470840 GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCACCCCCAGCGCACCTTTTACCCACACCACCCCC GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCGCCCCCAGCGCACCTTTTACCCACACCACCCCC A G PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131470764..131471003 26863196 MeRIP-seq:(Medium) rs1398997491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90929,Human_RBP_ID_713770 Human_Splice_Rec_1092156,Human_Splice_Rec_1092228,Human_Splice_Rec_1092274 Human_miRNA_ID_2143493,Human_miRNA_ID_2145024,Human_miRNA_ID_2684412,Human_miRNA_ID_2687529 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_11680,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_260469 107616 RMVar_ID_107616 Human_SNP_ID_416736854 m1A Human chr9 + 131470867 131470867 131470867 GTCCCACCCCCAGCGCACCTTTTACCCACACCACCCCCAGATGTTGGGCTTCGATCCCAGGTGGA GTCCCACCCCCAGCGCACCTTTTACCCACACCGCCCCCAGATGTTGGGCTTCGATCCCAGGTGGA A G PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:131470851..131470875 26863196 MeRIP-seq:(Medium) rs1187498893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90929,Human_RBP_ID_713771,Human_RBP_ID_2061654,Human_RBP_ID_3192026,Human_RBP_ID_3976061,Human_RBP_ID_5015288,Human_RBP_ID_9315293,Human_RBP_ID_18131226,Human_RBP_ID_22336663,Human_RBP_ID_22466249,Human_RBP_ID_27132035,Human_RBP_ID_27371677,Human_RBP_ID_27543249 Human_Splice_Rec_1092156,Human_Splice_Rec_1092228,Human_Splice_Rec_1092274 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_11680,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_260469 107617 RMVar_ID_107617 Human_SNP_ID_416737618 m1A Human chr9 + 131473601 131473601 131473601 TCAGAACTGTGTGCCCCCACTCCAAGAAAGAAAAGTGACCCCCATCGACTCACCCCCTGTGTGGA TCAGAACTGTGTGCCCCCACTCCAAGAAAGAAGAGTGACCCCCATCGACTCACCCCCTGTGTGGA A G PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131473551..131473617 26863196 MeRIP-seq:(Medium) rs752458711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963985,Human_RBP_ID_8926090,Human_RBP_ID_18196997 Human_Splice_Rec_1092158,Human_Splice_Rec_1092230 RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_30528,RMVar_hsa_circ_75527,RMVar_hsa_circ_260471 107618 RMVar_ID_107618 Human_SNP_ID_416738235 m1A Human chr9 - 131475167 131475167 131475167 CCTCCTCTTCAAATTTGGTGGCCTCGCGGCCAAAAGTGGCATGGCCAGGGCCTTTGTCCTCCAAA CCTCCTCTTCAAATTTGGTGGCCTCGCGGCCACAAGTGGCATGGCCAGGGCCTTTGTCCTCCAAA T G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:131475126..131475175 26863196 MeRIP-seq:(Medium) rs551677276 Functional Loss SNV dbSNP153 33..33 33 - - - 107619 RMVar_ID_107619 Human_SNP_ID_416738449 m1A Human chr9 + 131475599 131475599 131475599 GCGCCGCCGGCAGAGGGGCTCCGAGAACGGGAATGAAGGCTCGCTCCTGGAGAGGGAGGAGAGCA GCGCCGCCGGCAGAGGGGCTCCGAGAACGGGATTGAAGGCTCGCTCCTGGAGAGGGAGGAGAGCA A T PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:131475551..131475600 26863196 MeRIP-seq:(Medium) rs567765615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961732,Human_RBP_ID_1338148,Human_RBP_ID_1402703,Human_RBP_ID_2061676,Human_RBP_ID_5039987,Human_RBP_ID_5535134,Human_RBP_ID_9264710,Human_RBP_ID_9407692,Human_RBP_ID_18197187,Human_RBP_ID_18414439,Human_RBP_ID_19024489,Human_RBP_ID_22732837,Human_RBP_ID_26361331,Human_RBP_ID_27574879 RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_127632,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_19294,RMVar_hsa_circ_75527,RMVar_hsa_circ_260471,RMVar_hsa_circ_374930,RMVar_hsa_circ_260472,RMVar_hsa_circ_17056 107620 RMVar_ID_107620 Human_SNP_ID_416738716 m1A Human chr9 + 131476149 131476149 131476149 GAGGAGCCCCACCTGCTGGCAGGTCAGTGGCCAGGCAGGCCCAAACTGTGTTCTGGGGACAAGAG GAGGAGCCCCACCTGCTGGCAGGTCAGTGGCCCGGCAGGCCCAAACTGTGTTCTGGGGACAAGAG A C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:131476101..131476400 32194978 MeRIP-seq:(Medium) rs764709260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90943,Human_RBP_ID_27132082 Human_miRNA_ID_2674970,Human_miRNA_ID_2925722 RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_127632,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_19294,RMVar_hsa_circ_75527,RMVar_hsa_circ_260471,RMVar_hsa_circ_374930,RMVar_hsa_circ_260472,RMVar_hsa_circ_17056,RMVar_hsa_circ_260474,RMVar_hsa_circ_260473 107621 RMVar_ID_107621 Human_SNP_ID_416738833 m1A Human chr9 + 131476396 131476396 131476396 AGAAGAAGGAGCTGGCCAAGAGGAGCTTCTCCAGTCAGAGACCCGTGGTTGACAGACAGAGCCGA AGAAGAAGGAGCTGGCCAAGAGGAGCTTCTCCGGTCAGAGACCCGTGGTTGACAGACAGAGCCGA A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:131475971..131476475;chr9:131476199..131476500 26863196 MeRIP-seq:(Medium) rs1297443405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90944,Human_RBP_ID_963991,Human_RBP_ID_1702798,Human_RBP_ID_5154518,Human_RBP_ID_16601886,Human_RBP_ID_18197188,Human_RBP_ID_18414547,Human_RBP_ID_22733095,Human_RBP_ID_23090658,Human_RBP_ID_26361332,Human_RBP_ID_27543281,Human_RBP_ID_27574812 RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_127632,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_19294,RMVar_hsa_circ_75527,RMVar_hsa_circ_260471,RMVar_hsa_circ_374930,RMVar_hsa_circ_260472,RMVar_hsa_circ_17056,RMVar_hsa_circ_260473 107622 RMVar_ID_107622 Human_SNP_ID_416743066 m1A Human chr9 - 131489748 131489748 131489748 AGAGAGGGAGATGTGCTGGGGCAGGGCCCCCCAGGGGCACAGGCAGCACCTAGGCAGGGATGTGG AGAGAGGGAGATGTGCTGGGGCAGGGCCCCCCCGGGGCACAGGCAGCACCTAGGCAGGGATGTGG T G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131489703..131489957 26863196 MeRIP-seq:(Medium) rs1203111949 Functional Loss SNV dbSNP153 33..33 33 - - - 107623 RMVar_ID_107623 Human_SNP_ID_416744972 m1A Human chr9 - 131496004 131496004 131496004 GGTTGACAACGGAGCTTTCGGGAGTGGAGAGGAGGGAGGTCTCTCAGTCTGGGCCACGCATTTGG GGTTGACAACGGAGCTTTCGGGAGTGGAGAGGGGGGAGGTCTCTCAGTCTGGGCCACGCATTTGG T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:131495826..131496181 26863196 MeRIP-seq:(Medium) rs1190663042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260488 107624 RMVar_ID_107624 Human_SNP_ID_416744984 m1A Human chr9 - 131496040 131496040 131496040 AAGCGGGTCAATGCCATATATCCACGGGTGCAAGCTGGTTGACAACGGAGCTTTCGGGAGTGGAG AAGCGGGTCAATGCCATATATCCACGGGTGCAGGCTGGTTGACAACGGAGCTTTCGGGAGTGGAG T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:131495876..131496203 26863196 MeRIP-seq:(Medium) rs1237499628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260488 107625 RMVar_ID_107625 Human_SNP_ID_416747030 m1A Human chr9 - 131502976 131502976 131502976 TGGGCCGACGGTTGGGGGTGAGGCCGCTCGGCACTCCGCACCACCCACCGCCCTGCTCAACGTTC TGGGCCGACGGTTGGGGGTGAGGCCGCTCGGCCCTCCGCACCACCCACCGCCCTGCTCAACGTTC T G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:131502926..131503083;chr9:131502926..131503510 26863196 MeRIP-seq:(Medium) rs942890836 Functional Loss SNV dbSNP153 33..33 33 - - - 107626 RMVar_ID_107626 Human_SNP_ID_416747042 m1A Human chr9 - 131503001 131503001 131503001 CGGCAACGCCTCGGAACCGTCCGACTGGGCCGACGGTTGGGGGTGAGGCCGCTCGGCACTCCGCA CGGCAACGCCTCGGAACCGTCCGACTGGGCCGGCGGTTGGGGGTGAGGCCGCTCGGCACTCCGCA T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:131502951..131503714;chr9:131502951..131503168 26863196 MeRIP-seq:(Medium) rs1422118177 Functional Loss SNV dbSNP153 33..33 33 - - - 107627 RMVar_ID_107627 Human_SNP_ID_416753444 m1A Human chr9 - 131523152 131523151 131523152 TGCTCATTACGTACATTGACCAAGACCCTTCAACCTCATCCCGACCCCAGCACGGGTGTTCTTTG TGCTCATTACGTACATTGACCAAGACCCTTCA_CCTCATCCCGACCCCAGCACGGGTGTTCTTTG GT G RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:131523101..131523204 26863196 MeRIP-seq:(Medium) rs1383878472 Functional Loss DEL dbSNP153 33..33 33 - - - 107628 RMVar_ID_107628 Human_SNP_ID_416755863 m1A Human chr9 + 131530617 131530617 131530617 GCTGCCGCTGTTCCACCTCGTTCTGTCCCAGCAACTCCATGATCTTCTCACACACGGTCGACTGG GCTGCCGCTGTTCCACCTCGTTCTGTCCCAGCGACTCCATGATCTTCTCACACACGGTCGACTGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:131530490..131531275 26863196 MeRIP-seq:(Medium) rs745543390 Functional Loss SNV dbSNP153 33..33 33 - - - 107629 RMVar_ID_107629 Human_SNP_ID_416755866 m1A Human chr9 - 131530624 131530624 131530624 TGTGTCTCCAGTCGACCGTGTGTGAGAAGATCATGGAGTTGCTGGGACAGAACGAGGTGGAACAG TGTGTCTCCAGTCGACCGTGTGTGAGAAGATCGTGGAGTTGCTGGGACAGAACGAGGTGGAACAG T C UCK1 Ensembl:ENSG00000130717 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr9:131530505..131531275;chr9:131530490..131531275 26863196 MeRIP-seq:(Medium) rs1410743533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713910,Human_RBP_ID_5015958,Human_RBP_ID_8926335,Human_RBP_ID_16603245,Human_RBP_ID_18905173,Human_RBP_ID_19024504,Human_RBP_ID_24290199 Human_Splice_Rec_1092688,Human_Splice_Rec_1092700,Human_Splice_Rec_1092712,Human_Splice_Rec_1092726,Human_Splice_Rec_1092736,Human_Splice_Rec_1092750,Human_Splice_Rec_1092762 107630 RMVar_ID_107630 Human_SNP_ID_416779269 m1A Human chr9 - 131615768 131615768 131615768 GAAGGGCAGTCGGGATTTTTAGGAGCTAAAGGACAGGGAAAGCAAGTCAAGATGTTCCAAACAGA GAAGGGCAGTCGGGATTTTTAGGAGCTAAAGGCCAGGGAAAGCAAGTCAAGATGTTCCAAACAGA T G RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:131615766..131615887 26863196 MeRIP-seq:(Medium) rs147022373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16603443 RMVar_hsa_circ_114024,RMVar_hsa_circ_77326,RMVar_hsa_circ_260504,RMVar_hsa_circ_260505,RMVar_hsa_circ_64310,RMVar_hsa_circ_87180,RMVar_hsa_circ_260507,RMVar_hsa_circ_260508,RMVar_hsa_circ_112361 107631 RMVar_ID_107631 Human_SNP_ID_416807764 m1A Human chr9 + 131736207 131736207 131736207 GGAAGAGCCTCTTCTCCTCTGCAGGCCTGCCCACAAGCTCACCCTGGGAGCTCCCTAATCTGTCC GGAAGAGCCTCTTCTCCTCTGCAGGCCTGCCCCCAAGCTCACCCTGGGAGCTCCCTAATCTGTCC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:131736157..131736286 26863196 MeRIP-seq:(Medium) rs911552880 Functional Loss SNV dbSNP153 33..33 33 - - - 107632 RMVar_ID_107632 Human_SNP_ID_416807786 m1A Human chr9 + 131736275 131736275 131736275 TCTCTTCTACTCCCTACCTCCTCGTCATCTCTAGAAGCACTGTAGAGTTTAGAAAGCCTCCCCTG TCTCTTCTACTCCCTACCTCCTCGTCATCTCTGGAAGCACTGTAGAGTTTAGAAAGCCTCCCCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:131736266..131736361 26863196 MeRIP-seq:(Medium) rs779540270 Functional Loss SNV dbSNP153 33..33 33 - - - 107633 RMVar_ID_107633 Human_SNP_ID_416808806 m1A Human chr9 - 131740022 131740022 131740022 GCGGGCCGGGGGAGCGGCGGCGGGCGCGCGGGAGGCGGAGCGGCGGCGGCGGGCGCGGCGGGAGC GCGGGCCGGGGGAGCGGCGGCGGGCGCGCGGGTGGCGGAGCGGCGGCGGCGGGCGCGGCGGGAGC T A RAPGEF1 Ensembl:ENSG00000107263 Protein coding 5'UTR GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,H2O2 treatment;HEK293T,Starvation treatment chr9:131739874..131740074;chr9:131739924..131740074 26863410 MeRIP-seq:(Medium) rs958755883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256468,Human_RBP_ID_3908894,Human_RBP_ID_5035943,Human_RBP_ID_9315778,Human_RBP_ID_9339139,Human_RBP_ID_18427240,Human_RBP_ID_22732840 107634 RMVar_ID_107634 Human_SNP_ID_416942655 m1A Human chr9 + 132276075 132276075 132276075 ACACATGCTCCCTCATGACCATACCGGACCCAAAATGCACCAAGACCAGGGGATGCACTGCCCCA ACACATGCTCCCTCATGACCATACCGGACCCAGAATGCACCAAGACCAGGGGATGCACTGCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:132276071..132276136 26863196 MeRIP-seq:(Medium) rs1268827518 Functional Loss SNV dbSNP153 33..33 33 - - - 107635 RMVar_ID_107635 Human_SNP_ID_416961777 m1A Human chr9 - 132339948 132339948 132339948 AACAAAGATGTAAGACGTCCCAGAAAGAGAAAAATAAAAATCAGGACAAAGAAATACCGGAGATA AACAAAGATGTAAGACGTCCCAGAAAGAGAAAGATAAAAATCAGGACAAAGAAATACCGGAGATA T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:132339925..132340095 26863196 MeRIP-seq:(Medium) rs1005982883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16607086 RMVar_hsa_circ_119175,RMVar_hsa_circ_260529,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_260545,RMVar_hsa_circ_260551,RMVar_hsa_circ_317034,RMVar_hsa_circ_260555,RMVar_hsa_circ_288156,RMVar_hsa_circ_47717,RMVar_hsa_circ_302953,RMVar_hsa_circ_260557,RMVar_hsa_circ_322007,RMVar_hsa_circ_376472,RMVar_hsa_circ_45757 107636 RMVar_ID_107636 Human_SNP_ID_416966247 m1A Human chr9 - 132354924 132354924 132354924 GTATGGAGGTGGGCTAGAGGCCGACGCCAGCCAGAGAGCGGTGAGGGTAGCGGCGGGCTGGAGGC GTATGGAGGTGGGCTAGAGGCCGACGCCAGCCGGAGAGCGGTGAGGGTAGCGGCGGGCTGGAGGC T C SETX Ensembl:ENSG00000107290 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:132354711..132354950 26863196 MeRIP-seq:(Medium) rs1287056712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797234,Human_RBP_ID_5036528,Human_RBP_ID_5535167,Human_RBP_ID_8930312,Human_RBP_ID_9315322,Human_RBP_ID_18427241,Human_RBP_ID_27843665 Human_Splice_Rec_1093081 RMVar_hsa_circ_119175,RMVar_hsa_circ_260529 107637 RMVar_ID_107637 Human_SNP_ID_416966250 m1A Human chr9 - 132354928 132354928 132354928 CCCGGTATGGAGGTGGGCTAGAGGCCGACGCCAGCCAGAGAGCGGTGAGGGTAGCGGCGGGCTGG CCCGGTATGGAGGTGGGCTAGAGGCCGACGCCGGCCAGAGAGCGGTGAGGGTAGCGGCGGGCTGG T C SETX Ensembl:ENSG00000107290 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:132354801..132354965;chr9:132354711..132354961;chr9:132354696..132354929 26863196 MeRIP-seq:(Medium) rs902850726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_797234,Human_RBP_ID_5036528,Human_RBP_ID_5535167,Human_RBP_ID_8930312,Human_RBP_ID_9315322,Human_RBP_ID_18427241,Human_RBP_ID_27843665 Human_Splice_Rec_1093081 RMVar_hsa_circ_119175,RMVar_hsa_circ_260529 107638 RMVar_ID_107638 Human_SNP_ID_416971872 m1A Human chr9 - 132375854 132375854 132375854 ACATGGTGAAGACCTGTCACTATTAAAAATGCAAAAATTAGCCGGGTGTGGTAGTGCACACCTGT ACATGGTGAAGACCTGTCACTATTAAAAATGCGAAAATTAGCCGGGTGTGGTAGTGCACACCTGT T C TTF1 Ensembl:ENSG00000125482 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1752675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_187622,Human_miRNA_ID_982301,Human_miRNA_ID_987021 107639 RMVar_ID_107639 Human_SNP_ID_416979377 m1A Human chr9 + 132401950 132401950 132401950 CACTGCCCACTTGTGATCCTTCAGGCATGGCCAATGCCTCAAATTCCTGGTGATTGGACTTTTTC CACTGCCCACTTGTGATCCTTCAGGCATGGCCGATGCCTCAAATTCCTGGTGATTGGACTTTTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:132401900..132402148 32194978 MeRIP-seq:(Medium) rs1337681719 Functional Loss SNV dbSNP153 33..33 33 - - - 107640 RMVar_ID_107640 Human_SNP_ID_417049155 m1A Human chr9 + 132670541 132670541 132670541 GAGGGCGCTGGGGGTGGCGGCGGCGGTCCGGGAGGTGGTCGCGCGACTGCGTGGAGCGCCAGGGC GAGGGCGCTGGGGGTGGCGGCGGCGGTCCGGGGGGTGGTCGCGCGACTGCGTGGAGCGCCAGGGC A G GTF3C4 Ensembl:ENSG00000125484 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:132670476..132670750;chr9:132670476..132670658;chr9:132670470..132670878;chr9:132670476..132670838;chr9:132670476..132670819 26863196 MeRIP-seq:(Medium) rs1187603037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256616,Human_RBP_ID_286969,Human_RBP_ID_714028,Human_RBP_ID_798664,Human_RBP_ID_5016568,Human_RBP_ID_5329674,Human_RBP_ID_8930313,Human_RBP_ID_9315323,Human_RBP_ID_9355068,Human_RBP_ID_9442775,Human_RBP_ID_18427745,Human_RBP_ID_22628694 107641 RMVar_ID_107641 Human_SNP_ID_417049200 m1A Human chr9 - 132670624 132670624 132670624 CAGACGGCGCAGGCCCGTCGTCCGCGGGCCCCACCCGGGCCTGGTCGGCCGTGTTCATCTTCTCT CAGACGGCGCAGGCCCGTCGTCCGCGGGCCCCTCCCGGGCCTGGTCGGCCGTGTTCATCTTCTCT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:132670518..132670738 26863196 MeRIP-seq:(Medium) rs199984441 Functional Loss SNV dbSNP153 33..33 33 - - - 107642 RMVar_ID_107642 Human_SNP_ID_417049201 m1A Human chr9 - 132670624 132670624 132670624 CAGACGGCGCAGGCCCGTCGTCCGCGGGCCCCACCCGGGCCTGGTCGGCCGTGTTCATCTTCTCT CAGACGGCGCAGGCCCGTCGTCCGCGGGCCCCCCCCGGGCCTGGTCGGCCGTGTTCATCTTCTCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:132670518..132670738 26863196 MeRIP-seq:(Medium) rs199984441 Functional Loss SNV dbSNP153 33..33 33 - - - 107643 RMVar_ID_107643 Human_SNP_ID_417051598 m1A Human chr9 + 132679521 132679521 132679521 GAAGGCACTTCTTCCAAACAGGTGGTGAAGCAAGGCCTGCAGGAGAGGAGCAAGGAAGGAGATGT GAAGGCACTTCTTCCAAACAGGTGGTGAAGCACGGCCTGCAGGAGAGGAGCAAGGAAGGAGATGT A C GTF3C4 Ensembl:ENSG00000125484 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:132679476..132679683 26863196 MeRIP-seq:(Medium) rs760291993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5535168,Human_RBP_ID_7906238 Human_miRNA_ID_1965901,Human_miRNA_ID_2361358 RMVar_hsa_circ_28725,RMVar_hsa_circ_347874,RMVar_hsa_circ_113179,RMVar_hsa_circ_260583 107644 RMVar_ID_107644 Human_SNP_ID_417051605 m1A Human chr9 + 132679537 132679537 132679537 AACAGGTGGTGAAGCAAGGCCTGCAGGAGAGGAGCAAGGAAGGAGATGTAGAGGAGCCCACTGAT AACAGGTGGTGAAGCAAGGCCTGCAGGAGAGGCGCAAGGAAGGAGATGTAGAGGAGCCCACTGAT A C GTF3C4 Ensembl:ENSG00000125484 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:132679486..132679636 26863196 MeRIP-seq:(Medium) rs556897264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5535168,Human_RBP_ID_7906238,Human_RBP_ID_8930320 RMVar_hsa_circ_28725,RMVar_hsa_circ_347874,RMVar_hsa_circ_113179,RMVar_hsa_circ_260583 107645 RMVar_ID_107645 Human_SNP_ID_417102375 m1A Human chr9 - 132883970 132883969 132883970 GGAAGAGCTTGTACTTCTGCTCGATGCTGCGAAGGGATTCTTTCACCTCATTCATTGTCTTCCTC GGAAGAGCTTGTACTTCTGCTCGATGCTGCGA_GGGATTCTTTCACCTCATTCATTGTCTTCCTC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:132883885..132884028 26863196 MeRIP-seq:(Medium) rs1426360042 Functional Loss DEL dbSNP153 33..33 33 - - - 107646 RMVar_ID_107646 Human_SNP_ID_417102386 m1A Human chr9 + 132883982 132883982 132883982 GAATGAGGTGAAAGAATCCCTTCGCAGCATCGAGCAGAAGTACAAGCTCTTCCAGCAGCAGCAGC GAATGAGGTGAAAGAATCCCTTCGCAGCATCGTGCAGAAGTACAAGCTCTTCCAGCAGCAGCAGC A T SPACA9 Ensembl:ENSG00000165698 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:132883892..132884002 26863196 MeRIP-seq:(Medium) rs975388229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1093472,Human_Splice_Rec_1093478 RMVar_hsa_circ_87370,RMVar_hsa_circ_260586 107647 RMVar_ID_107647 Human_SNP_ID_417137736 m1A Human chr9 + 133019615 133019612 133019615 GCATCGACAAAAGAACCATTGAAAAATTTGAGAAGGAGGCTGCTGAGATGGGAAAGGGCTCCTTC GCATCGACAAAAGAACCATTGAAAAATTTG___AGGAGGCTGCTGAGATGGGAAAGGGCTCCTTC GAGA G EEF1A1P5 Ensembl:ENSG00000196205 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1258279182 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17437793 107648 RMVar_ID_107648 Human_SNP_ID_417141173 m1A Human chr9 + 133031073 133031073 133031073 GGGGGCCGCCGTCCCCGTGGAGCTGAGGCGGGAGCGACGCATGGTGTGCGTGGAGTACCCGGGAG GGGGGCCGCCGTCCCCGTGGAGCTGAGGCGGGGGCGACGCATGGTGTGCGTGGAGTACCCGGGAG A G GTF3C5 Ensembl:ENSG00000148308 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133031023..133042196 32194978 MeRIP-seq:(Medium) rs1403308442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256731,Human_RBP_ID_5036536,Human_RBP_ID_8930727,Human_RBP_ID_9339631,Human_RBP_ID_18427243,Human_RBP_ID_22628711,Human_RBP_ID_24291080,Human_RBP_ID_26566204 Human_Splice_Rec_1094697,Human_Splice_Rec_1094711,Human_Splice_Rec_1094735,Human_Splice_Rec_1094755,Human_Splice_Rec_1094773,Human_Splice_Rec_1094781 107649 RMVar_ID_107649 Human_SNP_ID_417141423 m1A Human chr9 + 133031863 133031852 133031863 GAGTGGCGGGGTGAGTAGTTTTGGTGGGAAGGATGGTTACAGAGCAGGTGACTCAGGATGACTAA GAGTGGCGGGGTGAGTAGTTTT___________TGGTTACAGAGCAGGTGACTCAGGATGACTAA TGGTGGGAAGGA T GTF3C5 Ensembl:ENSG00000148308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133031860..133031967 26863196 MeRIP-seq:(Medium) rs1256288185 Functional Loss DEL dbSNP153 23..33 33 - - - 107650 RMVar_ID_107650 Human_SNP_ID_417141427 m1A Human chr9 + 133031863 133031863 133031863 GAGTGGCGGGGTGAGTAGTTTTGGTGGGAAGGATGGTTACAGAGCAGGTGACTCAGGATGACTAA GAGTGGCGGGGTGAGTAGTTTTGGTGGGAAGGTTGGTTACAGAGCAGGTGACTCAGGATGACTAA A T GTF3C5 Ensembl:ENSG00000148308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133031860..133031967 26863196 MeRIP-seq:(Medium) rs773500808 Functional Loss SNV dbSNP153 33..33 33 - - - 107651 RMVar_ID_107651 Human_SNP_ID_417144524 m1A Human chr9 + 133043824 133043824 133043824 TGACAAGGTGCTCATGCTCCGGCCCGAGAAGGAGGCCTTTTTCCACCAGGAGCTGCCGCTCTACA TGACAAGGTGCTCATGCTCCGGCCCGAGAAGGCGGCCTTTTTCCACCAGGAGCTGCCGCTCTACA A C GTF3C5 Ensembl:ENSG00000148308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133043774..133043865 26863196 MeRIP-seq:(Medium) rs751042827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8699130,Human_RBP_ID_22337132,Human_RBP_ID_22838018,Human_RBP_ID_26833708 Human_Splice_Rec_1094714,Human_Splice_Rec_1094732,Human_Splice_Rec_1094738,Human_Splice_Rec_1094758,Human_Splice_Rec_1094774,Human_Splice_Rec_1094782 RMVar_hsa_circ_90557,RMVar_hsa_circ_101759,RMVar_hsa_circ_112831,RMVar_hsa_circ_127311,RMVar_hsa_circ_277857,RMVar_hsa_circ_111001,RMVar_hsa_circ_91387,RMVar_hsa_circ_260597,RMVar_hsa_circ_260599,RMVar_hsa_circ_260601,RMVar_hsa_circ_260603,RMVar_hsa_circ_76424,RMVar_hsa_circ_260602,RMVar_hsa_circ_260600,RMVar_hsa_circ_260598,RMVar_hsa_circ_111204,RMVar_hsa_circ_260596,RMVar_hsa_circ_356843,RMVar_hsa_circ_260605,RMVar_hsa_circ_108176,RMVar_hsa_circ_260606,RMVar_hsa_circ_260604 107652 RMVar_ID_107652 Human_SNP_ID_417144525 m1A Human chr9 + 133043824 133043824 133043824 TGACAAGGTGCTCATGCTCCGGCCCGAGAAGGAGGCCTTTTTCCACCAGGAGCTGCCGCTCTACA TGACAAGGTGCTCATGCTCCGGCCCGAGAAGGGGGCCTTTTTCCACCAGGAGCTGCCGCTCTACA A G GTF3C5 Ensembl:ENSG00000148308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133043774..133043865 26863196 MeRIP-seq:(Medium) rs751042827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8699130,Human_RBP_ID_22337132,Human_RBP_ID_22838018,Human_RBP_ID_26833708 Human_Splice_Rec_1094714,Human_Splice_Rec_1094732,Human_Splice_Rec_1094738,Human_Splice_Rec_1094758,Human_Splice_Rec_1094774,Human_Splice_Rec_1094782 RMVar_hsa_circ_90557,RMVar_hsa_circ_101759,RMVar_hsa_circ_112831,RMVar_hsa_circ_127311,RMVar_hsa_circ_277857,RMVar_hsa_circ_111001,RMVar_hsa_circ_91387,RMVar_hsa_circ_260597,RMVar_hsa_circ_260599,RMVar_hsa_circ_260601,RMVar_hsa_circ_260603,RMVar_hsa_circ_76424,RMVar_hsa_circ_260602,RMVar_hsa_circ_260600,RMVar_hsa_circ_260598,RMVar_hsa_circ_111204,RMVar_hsa_circ_260596,RMVar_hsa_circ_356843,RMVar_hsa_circ_260605,RMVar_hsa_circ_108176,RMVar_hsa_circ_260606,RMVar_hsa_circ_260604 107653 RMVar_ID_107653 Human_SNP_ID_417148939 m1A Human chr9 - 133058253 133058253 133058253 ACTGGTCTCATCCTGAGAGGCATTGGGTGCCCACTCACTGGCTGGATGCTGGGCTGGTTCATGGG ACTGGTCTCATCCTGAGAGGCATTGGGTGCCCGCTCACTGGCTGGATGCTGGGCTGGTTCATGGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:133058203..133058403 32194978 MeRIP-seq:(Medium) rs1445625294 Functional Loss SNV dbSNP153 33..33 33 - - - 107654 RMVar_ID_107654 Human_SNP_ID_417164492 m1A Human chr9 - 133108696 133108696 133108696 CCACCTTCTCCTGGCCCAGCTGGAGCACTCGGAACCCATTGAGGCAGAGCCTGAGGGTGAGGAGG CCACCTTCTCCTGGCCCAGCTGGAGCACTCGGGACCCATTGAGGCAGAGCCTGAGGGTGAGGAGG T C AL162417.1,RALGDS Ensembl:ENSG00000285245,Ensembl:ENSG00000160271 Protein coding,Protein coding CDS,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133108352..133108818 32194978 MeRIP-seq:(Medium) rs1482802229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1094857,Human_Splice_Rec_1094879,Human_Splice_Rec_1094907,Human_Splice_Rec_1094941,Human_Splice_Rec_1094975,Human_Splice_Rec_1095009,Human_Splice_Rec_1095043,Human_Splice_Rec_1095081,Human_Splice_Rec_1095169 Human_miRNA_ID_2395262,Human_miRNA_ID_3068995 RMVar_hsa_circ_16805,RMVar_hsa_circ_51863,RMVar_hsa_circ_260622,RMVar_hsa_circ_98896,RMVar_hsa_circ_260621,RMVar_hsa_circ_342047 107655 RMVar_ID_107655 Human_SNP_ID_417168117 m1A Human chr9 - 133121154 133121154 133121154 GGCCGGCCCCGCGCCCGCGCTGCGAGCCTTCCATGGTGCAGCGCATGTGGGCCGAGGCGGCCGGG GGCCGGCCCCGCGCCCGCGCTGCGAGCCTTCCGTGGTGCAGCGCATGTGGGCCGAGGCGGCCGGG T C AL162417.1,RALGDS Ensembl:ENSG00000285245,Ensembl:ENSG00000160271 Protein coding,Protein coding intron,exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:133121053..133121176 26863410 MeRIP-seq:(Medium) rs1281152456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5017092 RMVar_hsa_circ_92066,RMVar_hsa_circ_260623 107656 RMVar_ID_107656 Human_SNP_ID_417169138 m1A Human chr9 + 133124062 133124059 133124063 ACACACAGAGACACACAGAGAGACAGAGACACAGACACACACACACACAGACACAAAGATACACA ACACACAGAGACACACAGAGAGACAGAGAC____ACACACACACACACAGACACAAAGATACACA CACAG C RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133124059..133124231 26863196 MeRIP-seq:(Medium) rs1280758399 Functional Loss DEL dbSNP153 31..34 33 - - - 107657 RMVar_ID_107657 Human_SNP_ID_417169140 m1A Human chr9 + 133124062 133124061 133124063 ACACACAGAGACACACAGAGAGACAGAGACACAGACACACACACACACAGACACAAAGATACACA ACACACAGAGACACACAGAGAGACAGAGACAC__ACACACACACACACAGACACAAAGATACACA CAG C RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133124059..133124231 26863196 MeRIP-seq:(Medium) rs1213330538 Functional Loss DEL dbSNP153 33..34 33 - - - 107658 RMVar_ID_107658 Human_SNP_ID_417175729 m1A Human chr9 - 133149175 133149175 133149175 GAGGCCCGAGCGGCCGGAGCGCGGCGCGGCGCAGACAATGGGAGCGGCGCTGGCGGCTGCCGGGG GAGGCCCGAGCGGCCGGAGCGCGGCGCGGCGCGGACAATGGGAGCGGCGCTGGCGGCTGCCGGGG T C AL162417.1,RALGDS Ensembl:ENSG00000285245,Ensembl:ENSG00000160271 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133149133..133149211 26863196 MeRIP-seq:(Medium) rs1347326622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255697,Human_RBP_ID_8239378 RMVar_hsa_circ_92066,RMVar_hsa_circ_260623 107659 RMVar_ID_107659 Human_SNP_ID_417222210 m1A Human chr9 + 133331137 133331137 133331137 ACTCTGGATTTAATTCTTCCATCCCACTTTGTATCTTGCATTCACTTCACTCTCTCTCCAGCTTT ACTCTGGATTTAATTCTTCCATCCCACTTTGTGTCTTGCATTCACTTCACTCTCTCTCCAGCTTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133331087..133331223 26863196 MeRIP-seq:(Medium) rs1472697613 Functional Loss SNV dbSNP153 33..33 33 - - - 107660 RMVar_ID_107660 Human_SNP_ID_417222786 m1A Human chr9 - 133332339 133332339 133332339 CTGATGTCATACCTTCCTCCCAGGTGGAGGTGAGCGAAGACGAGCCGGCCAGCAAGGCGCAGCGC CTGATGTCATACCTTCCTCCCAGGTGGAGGTGTGCGAAGACGAGCCGGCCAGCAAGGCGCAGCGC T A SURF6 Ensembl:ENSG00000148296 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:133331715..133332775;chr9:133331926..133332802 26863196 MeRIP-seq:(Medium) rs1365217068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19025963,Human_RBP_ID_26361365 Human_Splice_Rec_1095416,Human_Splice_Rec_1095418 107661 RMVar_ID_107661 Human_SNP_ID_417223340 m1A Human chr9 + 133333779 133333778 133333780 GCAGTCGCTGTCGCAGAACATCCAGAGCAAAGACAGACTCAGGCTCAGTGGCCAGGCCATCTGCA GCAGTCGCTGTCGCAGAACATCCAGAGCAAAG__AGACTCAGGCTCAGTGGCCAGGCCATCTGCA GAC G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133333728..133336100 32194978 MeRIP-seq:(Medium) rs782181419 Functional Loss DEL dbSNP153 33..34 33 - - - 107662 RMVar_ID_107662 Human_SNP_ID_417223623 m1A Human chr9 - 133334564 133334564 133334564 AAAACTCAAGGCTCAGAAACTGCAGGGCCCCCAAAAAAGAAAAGGAAGAAAACACAAAAGAAATT AAAACTCAAGGCTCAGAAACTGCAGGGCCCCCCAAAAAGAAAAGGAAGAAAACACAAAAGAAATT T G SURF6 Ensembl:ENSG00000148296 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:133334463..133334563 32194978 MeRIP-seq:(Medium) rs201264112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26210740 Human_Splice_Rec_1095410 107663 RMVar_ID_107663 Human_SNP_ID_417224226 m1A Human chr9 + 133336153 133336153 133336153 TAGAGAGGCCATGGCGGAGACCCGGGCCGTTCACGACTCACACCTTCCCCGCTGCGCGTGCGACT TAGAGAGGCCATGGCGGAGACCCGGGCCGTTCCCGACTCACACCTTCCCCGCTGCGCGTGCGACT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133333660..133336200 26863196 MeRIP-seq:(Medium) rs947821238 Functional Loss SNV dbSNP153 33..33 33 - - - 107664 RMVar_ID_107664 Human_SNP_ID_417225609 m1A Human chr9 + 133341272 133341272 133341272 CTTCCACCTGGCTGGCCAGGAAGGCAGCAAACAGAGATGATGACTCGGAATGATGGGCTATTCGG CTTCCACCTGGCTGGCCAGGAAGGCAGCAAACGGAGATGATGACTCGGAATGATGGGCTATTCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133341101..133341350 26863196 MeRIP-seq:(Medium) rs899127619 Functional Loss SNV dbSNP153 33..33 33 - - - 107665 RMVar_ID_107665 Human_SNP_ID_417225718 m1A Human chr9 + 133341596 133341596 133341596 GTAGGGGGCCAGCACTGGGCTCCGGGGACGCCAGCAGAGGGGCCGAGAGGCCATCAGCAGAGTCT GTAGGGGGCCAGCACTGGGCTCCGGGGACGCCCGCAGAGGGGCCGAGAGGCCATCAGCAGAGTCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133341546..133341700 26863196 MeRIP-seq:(Medium) rs930725610 Functional Loss SNV dbSNP153 33..33 33 - - - 107666 RMVar_ID_107666 Human_SNP_ID_417225719 m1A Human chr9 + 133341596 133341596 133341596 GTAGGGGGCCAGCACTGGGCTCCGGGGACGCCAGCAGAGGGGCCGAGAGGCCATCAGCAGAGTCT GTAGGGGGCCAGCACTGGGCTCCGGGGACGCCGGCAGAGGGGCCGAGAGGCCATCAGCAGAGTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133341546..133341700 26863196 MeRIP-seq:(Medium) rs930725610 Functional Loss SNV dbSNP153 33..33 33 - - - 107667 RMVar_ID_107667 Human_SNP_ID_417225859 m1A Human chr9 - 133341965 133341965 133341965 TAGGCTAGGACAGGCCCACGTGGAGGCTGGGCAGGAAGGGCCTGCTGAGGTCACACAGCTGTTGG TAGGCTAGGACAGGCCCACGTGGAGGCTGGGCGGGAAGGGCCTGCTGAGGTCACACAGCTGTTGG T C MED22 Ensembl:ENSG00000148297 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133341759..133342259 26863196 MeRIP-seq:(Medium) rs1170051415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22337191,Human_RBP_ID_26566222 Human_miRNA_ID_462916,Human_miRNA_ID_929843 107668 RMVar_ID_107668 Human_SNP_ID_417225875 m1A Human chr9 + 133342037 133342037 133342037 CAGCTGGTGCTGGTCCCCCTCCTCTTGCAAAAAGCTGTCAGCCTGGCCACCCTCCCTCCTCCCTG CAGCTGGTGCTGGTCCCCCTCCTCTTGCAAAAGGCTGTCAGCCTGGCCACCCTCCCTCCTCCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133341851..133342070 26863196 MeRIP-seq:(Medium) rs1446420209 Functional Loss SNV dbSNP153 33..33 33 - - - 107669 RMVar_ID_107669 Human_SNP_ID_417227298 m1A Human chr9 + 133346675 133346675 133346675 AGGGCTCTCTGCTGGGCCATGGCCGAGCCTCAAGCAGCGCAGCGGGGAGACCTGGGACCTAGAGT AGGGCTCTCTGCTGGGCCATGGCCGAGCCTCAGGCAGCGCAGCGGGGAGACCTGGGACCTAGAGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133346544..133346732 26863196 MeRIP-seq:(Medium) rs782657285 Functional Loss SNV dbSNP153 33..33 33 - - - 107670 RMVar_ID_107670 Human_SNP_ID_417227313 m1A Human chr9 - 133346695 133346695 133346695 CACTCAGAGGTCTGTGCTGCACTCTAGGTCCCAGGTCTCCCCGCTGCGCTGCTTGAGGCTCGGCC CACTCAGAGGTCTGTGCTGCACTCTAGGTCCCCGGTCTCCCCGCTGCGCTGCTTGAGGCTCGGCC T G MED22 Ensembl:ENSG00000148297 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133346499..133346734 26863196 MeRIP-seq:(Medium) rs1564341429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036543,Human_RBP_ID_16610856,Human_RBP_ID_22630113 Human_Splice_Rec_1095420,Human_Splice_Rec_1095428,Human_Splice_Rec_1095436,Human_Splice_Rec_1095450,Human_Splice_Rec_1095456,Human_Splice_Rec_1095466,Human_Splice_Rec_1095472 RMVar_hsa_circ_308762 107671 RMVar_ID_107671 Human_SNP_ID_417227719 m1A Human chr9 - 133347962 133347962 133347962 GCAGAGGCACTTGACCACCCCGCCCTAGGCCGACCCGGCGGACGCGGCGTCTGGTGTGCGGGCGC GCAGAGGCACTTGACCACCCCGCCCTAGGCCGGCCCGGCGGACGCGGCGTCTGGTGTGCGGGCGC T C MED22 Ensembl:ENSG00000148297 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133347931..133348031 32194978 MeRIP-seq:(Medium) rs889244351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036544,Human_RBP_ID_18427244 Human_Splice_Rec_1095419,Human_Splice_Rec_1095435,Human_Splice_Rec_1095445,Human_Splice_Rec_1095449,Human_Splice_Rec_1095455,Human_Splice_Rec_1095465,Human_Splice_Rec_1095471 107672 RMVar_ID_107672 Human_SNP_ID_417227728 m1A Human chr9 - 133348006 133348006 133348006 GCGGGAGGGCCAGGCCGTGGGAGAGACGCGGGAAAGTGCGGGTCGCAGAGGCACTTGACCACCCC GCGGGAGGGCCAGGCCGTGGGAGAGACGCGGGTAAGTGCGGGTCGCAGAGGCACTTGACCACCCC T A MED22 Ensembl:ENSG00000148297 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133347747..133348131 26863196 MeRIP-seq:(Medium) rs1201143828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256730,Human_RBP_ID_3906493,Human_RBP_ID_5036545,Human_RBP_ID_18427244 Human_Splice_Rec_1095419,Human_Splice_Rec_1095435,Human_Splice_Rec_1095445,Human_Splice_Rec_1095449,Human_Splice_Rec_1095455,Human_Splice_Rec_1095465,Human_Splice_Rec_1095471 107673 RMVar_ID_107673 Human_SNP_ID_417227731 m1A Human chr9 - 133348027 133348027 133348027 CGGCGGGGAAGAGAGACTGCGGCGGGAGGGCCAGGCCGTGGGAGAGACGCGGGAAAGTGCGGGTC CGGCGGGGAAGAGAGACTGCGGCGGGAGGGCCCGGCCGTGGGAGAGACGCGGGAAAGTGCGGGTC T G MED22 Ensembl:ENSG00000148297 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:133347926..133348150 26863410 MeRIP-seq:(Medium) rs1196619551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256730,Human_RBP_ID_3906493,Human_RBP_ID_5036545,Human_RBP_ID_18427244 Human_Splice_Rec_1095449,Human_Splice_Rec_1095465 107674 RMVar_ID_107674 Human_SNP_ID_417228140 m1A Human chr9 - 133348761 133348761 133348761 TCTGCAACCCCCCAGCACCACCCCTCGACAGGAGCATCTCACATTCAGCCGCACAAGCATGCAGC TCTGCAACCCCCCAGCACCACCCCTCGACAGGGGCATCTCACATTCAGCCGCACAAGCATGCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133348759..133348939 26863196 MeRIP-seq:(Medium) rs782787215 Functional Loss SNV dbSNP153 33..33 33 - - - 107675 RMVar_ID_107675 Human_SNP_ID_417228774 m1A Human chr9 - 133350003 133350003 133350003 GGTCTCTTCGTTGGGACGTCCCCTTTGCCAGCAGCCTTCTTCTCGGCCCGGGCCAACAGTCTCTG GGTCTCTTCGTTGGGACGTCCCCTTTGCCAGCCGCCTTCTTCTCGGCCCGGGCCAACAGTCTCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133349953..133350099 26863196 MeRIP-seq:(Medium) rs782611553 Functional Loss SNV dbSNP153 33..33 33 - - - 107676 RMVar_ID_107676 Human_SNP_ID_417228782 m1A Human chr9 + 133350025 133350025 133350025 AGAAGAAGGCTGCTGGCAAAGGGGACGTCCCAACGAAGAGACCACCTGTCCTTCGAGCAGGTGAG AGAAGAAGGCTGCTGGCAAAGGGGACGTCCCAGCGAAGAGACCACCTGTCCTTCGAGCAGGTGAG A G RPL7A Ensembl:ENSG00000148303 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:133349918..133350118;chr9:133349951..133350025 32194978 MeRIP-seq:(Medium) rs782035629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91460,Human_RBP_ID_714248,Human_RBP_ID_1058470,Human_RBP_ID_2061997,Human_RBP_ID_5017316,Human_RBP_ID_8275160,Human_RBP_ID_8699218,Human_RBP_ID_9233826,Human_RBP_ID_17321581,Human_RBP_ID_18131778,Human_RBP_ID_18396911,Human_RBP_ID_18453274,Human_RBP_ID_18905572,Human_RBP_ID_19025969,Human_RBP_ID_22517960,Human_RBP_ID_22838057,Human_RBP_ID_23090906,Human_RBP_ID_23141424,Human_RBP_ID_27132699,Human_RBP_ID_27372197,Human_RBP_ID_27783898 Human_Splice_Rec_1095479,Human_Splice_Rec_1095489,Human_Splice_Rec_1095503,Human_Splice_Rec_1095513,Human_Splice_Rec_1095521,Human_Splice_Rec_1095536,Human_Splice_Rec_1095537,Human_Splice_Rec_1095549 Human_miRNA_ID_2890295 RMVar_hsa_circ_79026,RMVar_hsa_circ_101429,RMVar_hsa_circ_97402,RMVar_hsa_circ_107909,RMVar_hsa_circ_117888,RMVar_hsa_circ_108251,RMVar_hsa_circ_260629,RMVar_hsa_circ_260630,RMVar_hsa_circ_260628,RMVar_hsa_circ_260631,RMVar_hsa_circ_260634,RMVar_hsa_circ_86510,RMVar_hsa_circ_97013,RMVar_hsa_circ_260636,RMVar_hsa_circ_78005,RMVar_hsa_circ_260635,RMVar_hsa_circ_115668,RMVar_hsa_circ_260633,RMVar_hsa_circ_111790,RMVar_hsa_circ_260637,RMVar_hsa_circ_260638,RMVar_hsa_circ_260639 107677 RMVar_ID_107677 Human_SNP_ID_417228866 m1A Human chr9 + 133350196 133350196 133350196 TCAGCAGCTGAGCCCAGCAGCTTCTTGTGACTAGAGCAGGCCCTGTGAGTGCTCACAAAGTGGTT TCAGCAGCTGAGCCCAGCAGCTTCTTGTGACTGGAGCAGGCCCTGTGAGTGCTCACAAAGTGGTT A G RPL7A Ensembl:ENSG00000148303 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133350194..133350338 26863196 MeRIP-seq:(Medium) rs782548071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183328,Human_RBP_ID_3192999,Human_RBP_ID_16610917,Human_RBP_ID_22692117,Human_RBP_ID_23090910 RMVar_hsa_circ_79026,RMVar_hsa_circ_101429,RMVar_hsa_circ_97402,RMVar_hsa_circ_107909,RMVar_hsa_circ_117888,RMVar_hsa_circ_108251,RMVar_hsa_circ_260629,RMVar_hsa_circ_260630,RMVar_hsa_circ_260628,RMVar_hsa_circ_260631,RMVar_hsa_circ_260634,RMVar_hsa_circ_86510,RMVar_hsa_circ_97013,RMVar_hsa_circ_260636,RMVar_hsa_circ_260635,RMVar_hsa_circ_115668,RMVar_hsa_circ_111790,RMVar_hsa_circ_260637,RMVar_hsa_circ_260638,RMVar_hsa_circ_260639 107678 RMVar_ID_107678 Human_SNP_ID_417228986 m1A Human chr9 - 133350462 133350460 133350463 TTCAAGGTTGAATTCAGTGAGAGATTCACATCATTGCAAGAGCCACGCATGTGTTGGATCTGTGT TTCAAGGTTGAATTCAGTGAGAGATTCACAT___TGCAAGAGCCACGCATGTGTTGGATCTGTGT AATG A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:133350226..133350725 32194978 MeRIP-seq:(Medium) rs782528744 Functional Loss DEL dbSNP153 32..34 33 - - - 107679 RMVar_ID_107679 Human_SNP_ID_417228988 m1A Human chr9 - 133350462 133350462 133350462 TTCAAGGTTGAATTCAGTGAGAGATTCACATCATTGCAAGAGCCACGCATGTGTTGGATCTGTGT TTCAAGGTTGAATTCAGTGAGAGATTCACATCGTTGCAAGAGCCACGCATGTGTTGGATCTGTGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:133350226..133350725 32194978 MeRIP-seq:(Medium) rs782143733 Functional Loss SNV dbSNP153 33..33 33 - - - 107680 RMVar_ID_107680 Human_SNP_ID_417231445 m1A Human chr9 - 133356431 133356431 133356431 GCCGGGTGCGATGGCGGCGGTGGCTGCGTTGCAGCTGGGGCTGCGGGCGGCGGGGCTGGGACGGG GCCGGGTGCGATGGCGGCGGTGGCTGCGTTGCCGCTGGGGCTGCGGGCGGCGGGGCTGGGACGGG T G SURF1 Ensembl:ENSG00000148290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:133356208..133356475;chr9:133356166..133356447 26863196 MeRIP-seq:(Medium) rs1005430150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256715,Human_RBP_ID_5017370,Human_RBP_ID_9354970,Human_RBP_ID_22466643 Human_Splice_Rec_1095559,Human_Splice_Rec_1095575,Human_Splice_Rec_1095611 107681 RMVar_ID_107681 Human_SNP_ID_417231608 m1A Human chr9 + 133356633 133356633 133356633 GTTGCCGGGCGACGTGCGGGCGTTTCTGCGGGAGCACCCGAGCCTGCGGCTCCAGACGGACGCCC GTTGCCGGGCGACGTGCGGGCGTTTCTGCGGGCGCACCCGAGCCTGCGGCTCCAGACGGACGCCC A C SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133356551..133357115 26863196 MeRIP-seq:(Medium) rs1466914205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036549 Human_Splice_Rec_1095613,Human_Splice_Rec_1095623 107682 RMVar_ID_107682 Human_SNP_ID_417231609 m1A Human chr9 + 133356633 133356633 133356633 GTTGCCGGGCGACGTGCGGGCGTTTCTGCGGGAGCACCCGAGCCTGCGGCTCCAGACGGACGCCC GTTGCCGGGCGACGTGCGGGCGTTTCTGCGGGGGCACCCGAGCCTGCGGCTCCAGACGGACGCCC A G SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133356551..133357115 26863196 MeRIP-seq:(Medium) rs1466914205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5036549 Human_Splice_Rec_1095613,Human_Splice_Rec_1095623 107683 RMVar_ID_107683 Human_SNP_ID_417232058 m1A Human chr9 + 133357749 133357749 133357749 GTTGTTCTGCAAACTCACCCTGCGGCACATCAACAAGTGCCCAGAACACGTGCTGAGGCACACCC GTTGTTCTGCAAACTCACCCTGCGGCACATCAGCAAGTGCCCAGAACACGTGCTGAGGCACACCC A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1281926142 Functional Loss SNV dbSNP153 33..33 33 - - - 107684 RMVar_ID_107684 Human_SNP_ID_417232738 m1A Human chr9 + 133360006 133360003 133360006 TGGAGTACGTGCCTGCCTGCCTGGTGCACCGGAGGAGGAGGAGGGAGGACCAGATGGACGGTGAC TGGAGTACGTGCCTGCCTGCCTGGTGCACC___GGAGGAGGAGGGAGGACCAGATGGACGGTGAC CGGA C SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133359951..133361073 26863196 MeRIP-seq:(Medium) rs781867176 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_714295,Human_RBP_ID_21907286 Human_Splice_Rec_1095618,Human_Splice_Rec_1095628,Human_Splice_Rec_1095632 107685 RMVar_ID_107685 Human_SNP_ID_417233933 m1A Human chr9 - 133363302 133363301 133363303 AGAATCGATGGCTCAGTCTGCTCTGGAGCCACAGTCTGGCGTCTGACCCTTCAGTGCAGGCCAGC AGAATCGATGGCTCAGTCTGCTCTGGAGCCA__GTCTGGCGTCTGACCCTTCAGTGCAGGCCAGC CTG C SURF4 Ensembl:ENSG00000148248 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133363251..133363325 32194978 MeRIP-seq:(Medium) rs782034766 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_714351,Human_RBP_ID_1703186,Human_RBP_ID_8224730,Human_RBP_ID_16611353,Human_RBP_ID_17550765,Human_RBP_ID_26562147,Human_RBP_ID_27543666 RMVar_hsa_circ_86369,RMVar_hsa_circ_109052,RMVar_hsa_circ_260652,RMVar_hsa_circ_260653 107686 RMVar_ID_107686 Human_SNP_ID_417234010 m1A Human chr9 - 133363504 133363501 133363504 GCCCTGGGGGTGTCTCCATGGATGAGAAGAAGAAGGAGTGGTAACAGTCACAGATCCCTACCTGC GCCCTGGGGGTGTCTCCATGGATGAGAAGAAG___GAGTGGTAACAGTCACAGATCCCTACCTGC CCTT C SURF4 Ensembl:ENSG00000148248 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133363228..133363601 26863196 MeRIP-seq:(Medium) rs782142213 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_714357,Human_RBP_ID_2062023,Human_RBP_ID_5017504,Human_RBP_ID_7906822,Human_RBP_ID_16611363,Human_RBP_ID_18905604,Human_RBP_ID_22466647,Human_RBP_ID_22777104,Human_RBP_ID_24291294 Human_miRNA_ID_2037162,Human_miRNA_ID_2347864,Human_miRNA_ID_2708488 RMVar_hsa_circ_86369,RMVar_hsa_circ_109052,RMVar_hsa_circ_260652,RMVar_hsa_circ_260653 107687 RMVar_ID_107687 Human_SNP_ID_417234013 m1A Human chr9 - 133363504 133363504 133363504 GCCCTGGGGGTGTCTCCATGGATGAGAAGAAGAAGGAGTGGTAACAGTCACAGATCCCTACCTGC GCCCTGGGGGTGTCTCCATGGATGAGAAGAAGGAGGAGTGGTAACAGTCACAGATCCCTACCTGC T C SURF4 Ensembl:ENSG00000148248 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133363228..133363601 26863196 MeRIP-seq:(Medium) rs1269018821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714357,Human_RBP_ID_2062023,Human_RBP_ID_5017504,Human_RBP_ID_7906822,Human_RBP_ID_16611363,Human_RBP_ID_18905604,Human_RBP_ID_22466647,Human_RBP_ID_22777104,Human_RBP_ID_24291294 Human_miRNA_ID_2037162,Human_miRNA_ID_2347864,Human_miRNA_ID_2708488 RMVar_hsa_circ_86369,RMVar_hsa_circ_109052,RMVar_hsa_circ_260652,RMVar_hsa_circ_260653 107688 RMVar_ID_107688 Human_SNP_ID_417237613 m1A Human chr9 - 133376042 133376041 133376042 GCCGGCCGCCGGGCACTTCCTGTGGAGGCCGCAGCGGGTGCGGGCGCCGACGGGCGAGAGCCAGC GCCGGCCGCCGGGCACTTCCTGTGGAGGCCGC_GCGGGTGCGGGCGCCGACGGGCGAGAGCCAGC CT C SURF4 Ensembl:ENSG00000148248 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:133375945..133376045 26863410 MeRIP-seq:(Medium) rs1353452486 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_256713,Human_RBP_ID_798753,Human_RBP_ID_5035957,Human_RBP_ID_5329706,Human_RBP_ID_9339166,Human_RBP_ID_22466257 107689 RMVar_ID_107689 Human_SNP_ID_417239475 m1A Human chr9 - 133382559 133382559 133382561 ACACCATCACCATGACCACCATCACCATCATCACACCATCACCACCATCACCATTATCATCACCA ACACCATCACCATGACCACCATCACCATCACTCCACCATCACCACCATCACCATTATCATCACCA TGA GAG - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133382542..133382654 26863196 MeRIP-seq:(Medium) rs1564375424 Functional Loss MNV dbSNP153 31..33 33 - - - 107690 RMVar_ID_107690 Human_SNP_ID_417239853 m1A Human chr9 + 133383320 133383317 133383320 GATGATGTGATGGTGGTAATGGTGGTGGTGTGATGATGGTGGTGATGGTGATGGTGATGATGGTA GATGATGTGATGGTGGTAATGGTGGTGGTG___TGATGGTGGTGATGGTGATGGTGATGATGGTA GTGA G STKLD1 Ensembl:ENSG00000198870 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133383309..133383470 26863196 MeRIP-seq:(Medium) rs1293241873 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_36882 107691 RMVar_ID_107691 Human_SNP_ID_417247165 m1A Human chr9 - 133406719 133406719 133406719 TTGGGCCCGGATGGTCAGGGTGGGGAGCAGGGACGGCCATGGGCACGCCTGGCCACGCTTTACCG TTGGGCCCGGATGGTCAGGGTGGGGAGCAGGGGCGGCCATGGGCACGCCTGGCCACGCTTTACCG T C REXO4 Ensembl:ENSG00000148300 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133406669..133406769 26863196 MeRIP-seq:(Medium) rs961019571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9354978,Human_RBP_ID_17175394,Human_RBP_ID_22337265 107692 RMVar_ID_107692 Human_SNP_ID_417247276 m1A Human chr9 - 133407002 133407002 133407002 GGTGAAGAAGGAGTGGGAGAGCATGGCCCGAGACAGGCGCCCCCTGCTGACTGCTCCAGACCACT GGTGAAGAAGGAGTGGGAGAGCATGGCCCGAGTCAGGCGCCCCCTGCTGACTGCTCCAGACCACT T A REXO4 Ensembl:ENSG00000148300 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133406952..133407081 26863196 MeRIP-seq:(Medium) rs782220781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714399 Human_Splice_Rec_1095762,Human_Splice_Rec_1095776,Human_Splice_Rec_1095786 107693 RMVar_ID_107693 Human_SNP_ID_417250421 m1A Human chr9 - 133417855 133417855 133417855 GGGTCTCGGGTGGCCGCCGGCCCAGGCGCTGGACGGCAGCAGGATGGGGAAGGCGAAGGTCCCCG GGGTCTCGGGTGGCCGCCGGCCCAGGCGCTGGGCGGCAGCAGGATGGGGAAGGCGAAGGTCCCCG T C REXO4 Ensembl:ENSG00000148300 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:133417693..133418000;chr9:133417583..133418025;chr9:133417609..133418025 26863196 MeRIP-seq:(Medium) rs781968355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035958,Human_RBP_ID_9355079,Human_RBP_ID_26361379,Human_RBP_ID_27833591 107694 RMVar_ID_107694 Human_SNP_ID_417250455 m1A Human chr9 - 133417893 133417893 133417893 GCGCTTGTGCTGCCAGGGCGCCGGGCCCGGGGAGGCCGGGGTCTCGGGTGGCCGCCGGCCCAGGC GCGCTTGTGCTGCCAGGGCGCCGGGCCCGGGGTGGCCGGGGTCTCGGGTGGCCGCCGGCCCAGGC T A REXO4 Ensembl:ENSG00000148300 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:133417822..133417963 26863196 MeRIP-seq:(Medium) rs1564401331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035958,Human_RBP_ID_9339167,Human_RBP_ID_9355079,Human_RBP_ID_9407722,Human_RBP_ID_26361379,Human_RBP_ID_27832898 107695 RMVar_ID_107695 Human_SNP_ID_417253709 m1A Human chr9 + 133429001 133429001 133429001 AGCCCGCTGGGCCGCCCGCGCCACCCCTCCCTACGTCCGTCCCCACCTCTCCCTACGTCCGTCCC AGCCCGCTGGGCCGCCCGCGCCACCCCTCCCTGCGTCCGTCCCCACCTCTCCCTACGTCCGTCCC A G ADAMTS13 Ensembl:ENSG00000160323 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:133428901..133429050 26863410 MeRIP-seq:(Medium) rs587620968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094777 107696 RMVar_ID_107696 Human_SNP_ID_417253712 m1A Human chr9 + 133429013 133429013 133429013 CGCCCGCGCCACCCCTCCCTACGTCCGTCCCCACCTCTCCCTACGTCCGTCCCCACTCCGCATTC CGCCCGCGCCACCCCTCCCTACGTCCGTCCCCGCCTCTCCCTACGTCCGTCCCCACTCCGCATTC A G ADAMTS13 Ensembl:ENSG00000160323 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133428986..133429103 26863196 MeRIP-seq:(Medium) rs1377242325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17094777 107697 RMVar_ID_107697 Human_SNP_ID_417264550 m1A Human chr9 - 133464349 133464349 133464349 CCCCTGAAGCTGGGCTGGGCGCCTCTCTGTCCATCCCCCTTCCCTATCCACCACTGGCCAGCACA CCCCTGAAGCTGGGCTGGGCGCCTCTCTGTCCGTCCCCCTTCCCTATCCACCACTGGCCAGCACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133464345..133464485 26863196 MeRIP-seq:(Medium) rs971781595 Functional Loss SNV dbSNP153 33..33 33 - - - 107698 RMVar_ID_107698 Human_SNP_ID_417269288 m1A Human chr9 - 133479039 133479039 133479039 AGAGACCCGGCCATGCAGGAGCCGCTGCTGGGAGCCGAGGGCCCGGACTACGACACCTTCCCCGA AGAGACCCGGCCATGCAGGAGCCGCTGCTGGGCGCCGAGGGCCCGGACTACGACACCTTCCCCGA T G SLC2A6 Ensembl:ENSG00000160326 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:133478939..133479112;chr9:133478941..133479108 26863196 MeRIP-seq:(Medium) rs782580371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035961 Human_Splice_Rec_1096201,Human_Splice_Rec_1096217,Human_Splice_Rec_1096243,Human_Splice_Rec_1096249 107699 RMVar_ID_107699 Human_SNP_ID_417331598 m1A Human chr9 - 133696272 133696272 133696272 TTCGGGAAGTTCTACCTGGTGGGGCTGGATGCAAGGAAGGCTGCCGACTGGCTCTTCTCCGCAGA TTCGGGAAGTTCTACCTGGTGGGGCTGGATGCCAGGAAGGCTGCCGACTGGCTCTTCTCCGCAGA T G SARDH Ensembl:ENSG00000123453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133690401..133696281 32194978 MeRIP-seq:(Medium) rs1362529036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9408795,Human_RBP_ID_19025990 Human_Splice_Rec_1096478,Human_Splice_Rec_1096479,Human_Splice_Rec_1096518,Human_Splice_Rec_1096519,Human_Splice_Rec_1096534,Human_Splice_Rec_1096535,Human_Splice_Rec_1096566,Human_Splice_Rec_1096567,Human_Splice_Rec_1096608,Human_Splice_Rec_1096609 RMVar_hsa_circ_60837,RMVar_hsa_circ_356088,RMVar_hsa_circ_366740,RMVar_hsa_circ_70351 107700 RMVar_ID_107700 Human_SNP_ID_417333414 m1A Human chr9 - 133702950 133702945 133702951 GGACTACGCCTACCGCAGGCTGCTGGCAGACGAGTACACCTTCGCCTTCCCGCCCCACCACGACA GGACTACGCCTACCGCAGGCTGCTGGCAGAC______ACCTTCGCCTTCCCGCCCCACCACGACA TGTACTC T SARDH Ensembl:ENSG00000123453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133702934..133703034 32194978 MeRIP-seq:(Medium) rs760822129 Functional Loss DEL dbSNP153 32..37 33 - - - Human_Splice_Rec_1096476,Human_Splice_Rec_1096477,Human_Splice_Rec_1096516,Human_Splice_Rec_1096517,Human_Splice_Rec_1096533,Human_Splice_Rec_1096564,Human_Splice_Rec_1096565,Human_Splice_Rec_1096606,Human_Splice_Rec_1096607 RMVar_hsa_circ_60837,RMVar_hsa_circ_366740,RMVar_hsa_circ_70351 107701 RMVar_ID_107701 Human_SNP_ID_417336377 m1A Human chr9 + 133713119 133713114 133713119 CTCCCCCATCAGGGGCTTGTGGTCGGGCGTGAAGGATTCTGAAAGAAGGAGAGAGAGGCCTGGAG CTCCCCCATCAGGGGCTTGTGGTCGGGC_____GGATTCTGAAAGAAGGAGAGAGAGGCCTGGAG CGTGAA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133713046..133718363 32194978 MeRIP-seq:(Medium) rs1564282784 Functional Loss DEL dbSNP153 29..33 33 - - - 107702 RMVar_ID_107702 Human_SNP_ID_417350049 m1A Human chr9 + 133762941 133762941 133762941 CTGTTACCAGGTCTCATGCAACATCAGGGTAGAGAAACCAGGGTCTGGCTAACCCAGCCAGAAGT CTGTTACCAGGTCTCATGCAACATCAGGGTAGGGAAACCAGGGTCTGGCTAACCCAGCCAGAAGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133762840..133762941 32194978 MeRIP-seq:(Medium) rs1462466203 Functional Loss SNV dbSNP153 33..33 33 - - - 107703 RMVar_ID_107703 Human_SNP_ID_417352619 m1A Human chr9 - 133772154 133772154 133772154 GACAGGGCTGACAGGGAGTGGCCCTGGGGGCCAGGGACGAGGGGCTTTGCTGCAGCAAACACAGA GACAGGGCTGACAGGGAGTGGCCCTGGGGGCCGGGGACGAGGGGCTTTGCTGCAGCAAACACAGA T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133772148..133772599 26863196 MeRIP-seq:(Medium) rs1333901774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5408898 RMVar_hsa_circ_76051,RMVar_hsa_circ_268841,RMVar_hsa_circ_46810,RMVar_hsa_circ_10082,RMVar_hsa_circ_29896,RMVar_hsa_circ_260666,RMVar_hsa_circ_106936,RMVar_hsa_circ_260667 107704 RMVar_ID_107704 Human_SNP_ID_417353693 m1A Human chr9 + 133776039 133776039 133776039 TGCAGCCCACGATCCACTCACCAGGGGTATGCAGTGTAGTCGATCTCCCGGGATGGCGGCCGGCT TGCAGCCCACGATCCACTCACCAGGGGTATGCGGTGTAGTCGATCTCCCGGGATGGCGGCCGGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133776031..133783511 32194978 MeRIP-seq:(Medium) rs750193368 Functional Loss SNV dbSNP153 33..33 33 - - - 107705 RMVar_ID_107705 Human_SNP_ID_417358701 m1A Human chr9 + 133791933 133791933 133791933 GTGCTGGGTGGGGTGTGTGTGACTGTGTGTGTAAGCAGGCTGTACTGGGTGGGGTGTGTGTGCAT GTGCTGGGTGGGGTGTGTGTGACTGTGTGTGTGAGCAGGCTGTACTGGGTGGGGTGTGTGTGCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133791928..133792015 26863196 MeRIP-seq:(Medium) rs1221361772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260679 107706 RMVar_ID_107706 Human_SNP_ID_417364810 m1A Human chr9 - 133812196 133812196 133812196 CCTCCTGTGCAGCGAGCATGACCTGGGGGAGGACATCTACGACTGCGTCCCGTGTGAGGATGGAG CCTCCTGTGCAGCGAGCATGACCTGGGGGAGGGCATCTACGACTGCGTCCCGTGTGAGGATGGAG T C VAV2 Ensembl:ENSG00000160293 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133812146..133861222 32194978 MeRIP-seq:(Medium) rs769233434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9408814 Human_Splice_Rec_1096642,Human_Splice_Rec_1096643,Human_Splice_Rec_1096694,Human_Splice_Rec_1096695,Human_Splice_Rec_1096752,Human_Splice_Rec_1096753 RMVar_hsa_circ_76051,RMVar_hsa_circ_268841,RMVar_hsa_circ_260666,RMVar_hsa_circ_90984,RMVar_hsa_circ_127563,RMVar_hsa_circ_260668,RMVar_hsa_circ_260669,RMVar_hsa_circ_57164,RMVar_hsa_circ_75896,RMVar_hsa_circ_99992,RMVar_hsa_circ_260671,RMVar_hsa_circ_260672,RMVar_hsa_circ_367275,RMVar_hsa_circ_92751,RMVar_hsa_circ_260675,RMVar_hsa_circ_260676,RMVar_hsa_circ_80049,RMVar_hsa_circ_260678,RMVar_hsa_circ_14534,RMVar_hsa_circ_340893,RMVar_hsa_circ_353687,RMVar_hsa_circ_260681,RMVar_hsa_circ_260683,RMVar_hsa_circ_94830,RMVar_hsa_circ_359935,RMVar_hsa_circ_302213,RMVar_hsa_circ_376386,RMVar_hsa_circ_260682,RMVar_hsa_circ_308002,RMVar_hsa_circ_276328,RMVar_hsa_circ_260687,RMVar_hsa_circ_260689,RMVar_hsa_circ_260688,RMVar_hsa_circ_260686,RMVar_hsa_circ_260690,RMVar_hsa_circ_369272,RMVar_hsa_circ_361686 107707 RMVar_ID_107707 Human_SNP_ID_417367625 m1A Human chr9 - 133821896 133821896 133821896 CTCCCAGAAAACAGCAGGAGTGAAAGGATGAGACGGGGCAGGAAGGAAGGAGGGGTGGTCACTGG CTCCCAGAAAACAGCAGGAGTGAAAGGATGAGGCGGGGCAGGAAGGAAGGAGGGGTGGTCACTGG T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133821892..133822036 26863196 MeRIP-seq:(Medium) rs1260332144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127563,RMVar_hsa_circ_260669,RMVar_hsa_circ_99992,RMVar_hsa_circ_260671,RMVar_hsa_circ_367275,RMVar_hsa_circ_260676,RMVar_hsa_circ_14534,RMVar_hsa_circ_353687,RMVar_hsa_circ_260681,RMVar_hsa_circ_94830,RMVar_hsa_circ_302213,RMVar_hsa_circ_376386,RMVar_hsa_circ_260682,RMVar_hsa_circ_308002,RMVar_hsa_circ_260687,RMVar_hsa_circ_260689,RMVar_hsa_circ_260688 107708 RMVar_ID_107708 Human_SNP_ID_417374855 m1A Human chr9 - 133846580 133846580 133846580 CCTGGGGAACTGCTTGGCGGCCCTGGATAGAGAGCGGCCGGGGCCAGGGCAGCCAGGGACAGGGC CCTGGGGAACTGCTTGGCGGCCCTGGATAGAGGGCGGCCGGGGCCAGGGCAGCCAGGGACAGGGC T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133846572..133846783 26863196 MeRIP-seq:(Medium) rs892334702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227238,Human_RBP_ID_8223605,Human_RBP_ID_8731328,Human_RBP_ID_22733536 RMVar_hsa_circ_127563,RMVar_hsa_circ_260669,RMVar_hsa_circ_99992,RMVar_hsa_circ_260671,RMVar_hsa_circ_353687,RMVar_hsa_circ_260681,RMVar_hsa_circ_94830,RMVar_hsa_circ_302213,RMVar_hsa_circ_376386,RMVar_hsa_circ_260682,RMVar_hsa_circ_260689,RMVar_hsa_circ_260688,RMVar_hsa_circ_260692,RMVar_hsa_circ_306860,RMVar_hsa_circ_295080,RMVar_hsa_circ_260691 107709 RMVar_ID_107709 Human_SNP_ID_417396263 m1A Human chr9 + 133919114 133919114 133919114 TTTTTAAAGACTTCCCCACATCCCATCCTCACACTTTCTTCACTGACCTAGCTCCGCCCTCTCCA TTTTTAAAGACTTCCCCACATCCCATCCTCACGCTTTCTTCACTGACCTAGCTCCGCCCTCTCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133919103..133919209 26863196 MeRIP-seq:(Medium) rs1287807480 Functional Loss SNV dbSNP153 33..33 33 - - - 107710 RMVar_ID_107710 Human_SNP_ID_417398444 m1A Human chr9 - 133927594 133927594 133927594 CTCCAGACAGAAAGGCAAGGGTGCAGGGGGTGAGTTGGGGTGCTGGGTGTGGGTGTGTGGCCAAG CTCCAGACAGAAAGGCAAGGGTGCAGGGGGTGCGTTGGGGTGCTGGGTGTGGGTGTGTGGCCAAG T G VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133927568..133927690 26863196 MeRIP-seq:(Medium) rs906540915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227941,Human_RBP_ID_8223693,Human_RBP_ID_9441820 RMVar_hsa_circ_376386,RMVar_hsa_circ_260689,RMVar_hsa_circ_260692,RMVar_hsa_circ_295080,RMVar_hsa_circ_311197,RMVar_hsa_circ_260693,RMVar_hsa_circ_260695,RMVar_hsa_circ_123034 107711 RMVar_ID_107711 Human_SNP_ID_417399159 m1A Human chr9 - 133930359 133930357 133930359 CAGGAGGCAGCAAGGAGGCAGGGAGGGTAGTGAAGAGGCCAGGAGGCAGCAAGGCTGCTGGGAGG CAGGAGGCAGCAAGGAGGCAGGGAGGGTAGTG__GAGGCCAGGAGGCAGCAAGGCTGCTGGGAGG CTT C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133930121..133930486 26863196 MeRIP-seq:(Medium) rs35311721 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8223704,Human_RBP_ID_24393522 RMVar_hsa_circ_376386,RMVar_hsa_circ_260689,RMVar_hsa_circ_260692,RMVar_hsa_circ_295080,RMVar_hsa_circ_311197,RMVar_hsa_circ_260693,RMVar_hsa_circ_260695,RMVar_hsa_circ_123034 107712 RMVar_ID_107712 Human_SNP_ID_417399163 m1A Human chr9 - 133930359 133930359 133930359 CAGGAGGCAGCAAGGAGGCAGGGAGGGTAGTGAAGAGGCCAGGAGGCAGCAAGGCTGCTGGGAGG CAGGAGGCAGCAAGGAGGCAGGGAGGGTAGTGGAGAGGCCAGGAGGCAGCAAGGCTGCTGGGAGG T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133930121..133930486 26863196 MeRIP-seq:(Medium) rs77717726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8223704,Human_RBP_ID_24393522 RMVar_hsa_circ_376386,RMVar_hsa_circ_260689,RMVar_hsa_circ_260692,RMVar_hsa_circ_295080,RMVar_hsa_circ_311197,RMVar_hsa_circ_260693,RMVar_hsa_circ_260695,RMVar_hsa_circ_123034 107713 RMVar_ID_107713 Human_SNP_ID_417399189 m1A Human chr9 - 133930414 133930414 133930414 AGAGGCAATGAGGATGCCGGAGGACAGTGAGGATGCTAGGAGCCAGTGTGGAGGCCAGGAGGCAG AGAGGCAATGAGGATGCCGGAGGACAGTGAGGGTGCTAGGAGCCAGTGTGGAGGCCAGGAGGCAG T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133930173..133930496 26863196 MeRIP-seq:(Medium) rs917271565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16612393 RMVar_hsa_circ_376386,RMVar_hsa_circ_260689,RMVar_hsa_circ_260692,RMVar_hsa_circ_295080,RMVar_hsa_circ_311197,RMVar_hsa_circ_260693,RMVar_hsa_circ_260695,RMVar_hsa_circ_123034 107714 RMVar_ID_107714 Human_SNP_ID_417406858 m1A Human chr9 - 133955837 133955827 133955837 TTTAGAGGGCTCCCCTCGGGCTGGGGGAGGCCAGAGCTGTGGGGAGGAGTGGGGAGGAGTAGGAG TTTAGAGGGCTCCCCTCGGGCTGGGGGAGGCC__________GGAGGAGTGGGGAGGAGTAGGAG CCCACAGCTCT C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133955825..133956093 26863196 MeRIP-seq:(Medium) rs1293715196 Functional Loss DEL dbSNP153 33..42 33 - - - 107715 RMVar_ID_107715 Human_SNP_ID_417407222 m1A Human chr9 + 133957018 133957006 133957018 ACTGCAGCACCCACCCACCTGCCCAGCTCCCCACCCAGCTCCCCACCTGCCCGGGGTACCCAGGA ACTGCAGCACCCACCCACCTG____________CCCAGCTCCCCACCTGCCCGGGGTACCCAGGA GCCCAGCTCCCCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133957010..133957108 26863196 MeRIP-seq:(Medium) rs377368697 Functional Loss DEL dbSNP153 22..33 33 - - - 107716 RMVar_ID_107716 Human_SNP_ID_417408371 m1A Human chr9 + 133961058 133961058 133961058 CTGGGAGCGCAGGTGAGGGAGCAGGGGCCTCCACTGGCCCACACCCGGCACACATCACGGGCGGC CTGGGAGCGCAGGTGAGGGAGCAGGGGCCTCCGCTGGCCCACACCCGGCACACATCACGGGCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:133961056..133961158 26863196 MeRIP-seq:(Medium) rs1425624790 Functional Loss SNV dbSNP153 33..33 33 - - - 107717 RMVar_ID_107717 Human_SNP_ID_417410835 m1A Human chr9 - 133969660 133969660 133969660 ATGAAGAGGGTGCTCTGGGGTCAGGCTTGAGCAGTGCGATGGACAGTGGGGCTCATCTGGAGTTG ATGAAGAGGGTGCTCTGGGGTCAGGCTTGAGCTGTGCGATGGACAGTGGGGCTCATCTGGAGTTG T A VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133969642..133970090 26863196 MeRIP-seq:(Medium) rs960741269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3907607,Human_RBP_ID_8223787,Human_RBP_ID_9441839,Human_RBP_ID_18962490,Human_RBP_ID_22419432,Human_RBP_ID_22733597 107718 RMVar_ID_107718 Human_SNP_ID_417410851 m1A Human chr9 - 133969732 133969732 133969732 ATGGAGAGAGATGGACGGCCCCGCTGGAGCGCAGGAGGAGTGGGTGGGCTTGGGGTGGATTGGAC ATGGAGAGAGATGGACGGCCCCGCTGGAGCGCGGGAGGAGTGGGTGGGCTTGGGGTGGATTGGAC T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133969683..133969840 26863196 MeRIP-seq:(Medium) rs1176221245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227269,Human_RBP_ID_8223787,Human_RBP_ID_18962490 107719 RMVar_ID_107719 Human_SNP_ID_417410852 m1A Human chr9 - 133969732 133969732 133969732 ATGGAGAGAGATGGACGGCCCCGCTGGAGCGCAGGAGGAGTGGGTGGGCTTGGGGTGGATTGGAC ATGGAGAGAGATGGACGGCCCCGCTGGAGCGCCGGAGGAGTGGGTGGGCTTGGGGTGGATTGGAC T G VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133969683..133969840 26863196 MeRIP-seq:(Medium) rs1176221245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227269,Human_RBP_ID_8223787,Human_RBP_ID_18962490 107720 RMVar_ID_107720 Human_SNP_ID_417414699 m1A Human chr9 - 133982489 133982489 133982489 GCCCCTCCAGCCAGTCTGCCGCGCCCCATCCTAGGCCCCCTCTTGGGGCCTCCTGCCCTGCCAGC GCCCCTCCAGCCAGTCTGCCGCGCCCCATCCTGGGCCCCCTCTTGGGGCCTCCTGCCCTGCCAGC T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:133982478..133982620 26863196 MeRIP-seq:(Medium) rs548441161 Functional Loss SNV dbSNP153 33..33 33 - - - 107721 RMVar_ID_107721 Human_SNP_ID_417414973 m1A Human chr9 + 133983478 133983478 133983478 GGCCCCCACCAAGGTCCTGCCTCCATGAGTCCACCGCCCTGAGGCCAGGGCCCCGACCCATCTCC GGCCCCCACCAAGGTCCTGCCTCCATGAGTCCGCCGCCCTGAGGCCAGGGCCCCGACCCATCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133983474..133983727 26863196 MeRIP-seq:(Medium) rs1046644189 Functional Loss SNV dbSNP153 33..33 33 - - - 107722 RMVar_ID_107722 Human_SNP_ID_417414994 m1A Human chr9 + 133983533 133983533 133983533 ACCCATCTCCAAGTCCCAAACCGCAGGCAGACACGGGTCACTCTCACGGCGGCCCCCACACCTCA ACCCATCTCCAAGTCCCAAACCGCAGGCAGACGCGGGTCACTCTCACGGCGGCCCCCACACCTCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133983482..133983638 26863196 MeRIP-seq:(Medium) rs1417331513 Functional Loss SNV dbSNP153 33..33 33 - - - 107723 RMVar_ID_107723 Human_SNP_ID_417417659 m1A Human chr9 - 133992687 133992687 133992687 GCGGCCCAGGCCCGGGACGCGCGGAGCGAGCGACCCCGCCGGGCCTTTGTCTCGGGCGGGGCAGG GCGGCCCAGGCCCGGGACGCGCGGAGCGAGCGCCCCCGCCGGGCCTTTGTCTCGGGCGGGGCAGG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:133992637..133992763 26863196 MeRIP-seq:(Medium) rs930154437 Functional Loss SNV dbSNP153 33..33 33 - - - 107724 RMVar_ID_107724 Human_SNP_ID_417427497 m1A Human chr9 + 134027145 134027144 134027146 ACGTGAAGATCAAACTGTGGTGTAAGAACCCAAGAAGCGCAGAATTGGCCCCCGAACCCCTCAGC ACGTGAAGATCAAACTGTGGTGTAAGAACCCA__AAGCGCAGAATTGGCCCCCGAACCCCTCAGC AAG A BRD3OS Ensembl:ENSG00000235106 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr9:134027094..134027232;chr9:134027094..134027195 26863196,32194978 MeRIP-seq:(Medium) rs1459643028 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_714477,Human_RBP_ID_16612451,Human_RBP_ID_27372340 107725 RMVar_ID_107725 Human_SNP_ID_417427498 m1A Human chr9 + 134027145 134027145 134027145 ACGTGAAGATCAAACTGTGGTGTAAGAACCCAAGAAGCGCAGAATTGGCCCCCGAACCCCTCAGC ACGTGAAGATCAAACTGTGGTGTAAGAACCCAGGAAGCGCAGAATTGGCCCCCGAACCCCTCAGC A G BRD3OS Ensembl:ENSG00000235106 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr9:134027094..134027232;chr9:134027094..134027195 26863196,32194978 MeRIP-seq:(Medium) rs1009344966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714477,Human_RBP_ID_16612451,Human_RBP_ID_27372340 107726 RMVar_ID_107726 Human_SNP_ID_417427734 m1A Human chr9 + 134027983 134027981 134027983 ACTGTCGCTGCCACAGCTGGCCACCTGTGTTCAGTCTCCATGAAGGATTCACCTTCTGCTCTCAC ACTGTCGCTGCCACAGCTGGCCACCTGTGTT__GTCTCCATGAAGGATTCACCTTCTGCTCTCAC TCA T BRD3OS Ensembl:ENSG00000235106 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:134027844..134028044 32194978 MeRIP-seq:(Medium) rs1453505933 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_714494,Human_RBP_ID_17548934 107727 RMVar_ID_107727 Human_SNP_ID_417428715 m1A Human chr9 + 134031297 134031297 134031297 GCTCCCCCGACGGCTCACACAGGCAGCACCTCACTGCCCTGTGGCTGGAGGGGCATTGCAAGGAG GCTCCCCCGACGGCTCACACAGGCAGCACCTCGCTGCCCTGTGGCTGGAGGGGCATTGCAAGGAG A G BRD3OS Ensembl:ENSG00000235106 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134031249..134031376 26863196 MeRIP-seq:(Medium) rs1337289607 Functional Loss SNV dbSNP153 33..33 33 - - - 107728 RMVar_ID_107728 Human_SNP_ID_417429300 m1A Human chr9 + 134033008 134033008 134033008 GGAGAACGCACATCCCACCCGACCACCCCCCAAGGGCTCCACGCTCCGGGCTGGGGCTGCGATGA GGAGAACGCACATCCCACCCGACCACCCCCCAGGGGCTCCACGCTCCGGGCTGGGGCTGCGATGA A G BRD3OS Ensembl:ENSG00000235106 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134032960..134033087 26863196 MeRIP-seq:(Medium) rs1260828622 Functional Loss SNV dbSNP153 33..33 33 - - - 107729 RMVar_ID_107729 Human_SNP_ID_417431426 m1A Human chr9 - 134040179 134040158 134040179 AGAAGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAG AGAAGAAGAAGGAGAAGAAGGAGAAGGAGAAG_____________________GAGAAGGAGAAG CCTTCTCCTTGTCCTTCTTCTT C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134040026..134045356 26863196 MeRIP-seq:(Medium) rs1217007600 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017967,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 107730 RMVar_ID_107730 Human_SNP_ID_417431426 m1A Human chr9 - 134040178 134040158 134040179 GAAGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAGC GAAGAAGAAGGAGAAGAAGGAGAAGGAGAAG_____________________GAGAAGGAGAAGC CCTTCTCCTTGTCCTTCTTCTT C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134040051..134041914 26863196 MeRIP-seq:(Medium) rs1217007600 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017964,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 107731 RMVar_ID_107731 Human_SNP_ID_417431433 m1A Human chr9 - 134040176 134040164 134040176 AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAGCAC AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAG____________GAGAAGGAGAAGGAGAAGCAC CCTTGTCCTTCTT C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134040026..134041914 26863196 MeRIP-seq:(Medium) rs1564549199 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017964,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 107732 RMVar_ID_107732 Human_SNP_ID_417431440 m1A Human chr9 - 134040176 134040176 134040176 AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAGCAC AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGGAGAAGGACAAGGAGAAGGAGAAGGAGAAGCAC T C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134040026..134041914 26863196 MeRIP-seq:(Medium) rs1564549210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017964,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 107733 RMVar_ID_107733 Human_SNP_ID_417431442 m1A Human chr9 - 134040179 134040179 134040179 AGAAGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAG AGAAGAAGAAGGAGAAGAAGGAGAAGGAGAAGGAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAG T C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134040026..134045356 26863196 MeRIP-seq:(Medium) rs765658761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017967,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 107734 RMVar_ID_107734 Human_SNP_ID_417434702 m1A Human chr9 - 134050443 134050435 134050443 ACTGCAAACGTCACGTCGGTCCCAGTCCCCCCAGCTGCCGCCCCACCTCCTCCTGCCACACCCAT ACTGCAAACGTCACGTCGGTCCCAGTCCCCCC________CCCCACCTCCTCCTGCCACACCCAT GCGGCAGCT G BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr9:134048316..134050600;chr9:134050376..134050575 26863196 MeRIP-seq:(Medium) rs146285241 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_847282,Human_RBP_ID_17437271,Human_RBP_ID_18963218 Human_Splice_Rec_1096833,Human_Splice_Rec_1096861,Human_Splice_Rec_1096871 Human_miRNA_ID_2386762,Human_miRNA_ID_2388237,Human_miRNA_ID_2399389,Human_miRNA_ID_2684425,Human_miRNA_ID_3030440 RMVar_hsa_circ_54565,RMVar_hsa_circ_81050,RMVar_hsa_circ_260697,RMVar_hsa_circ_260698,RMVar_hsa_circ_373881 107735 RMVar_ID_107735 Human_SNP_ID_417434708 m1A Human chr9 - 134050443 134050443 134050443 ACTGCAAACGTCACGTCGGTCCCAGTCCCCCCAGCTGCCGCCCCACCTCCTCCTGCCACACCCAT ACTGCAAACGTCACGTCGGTCCCAGTCCCCCCGGCTGCCGCCCCACCTCCTCCTGCCACACCCAT T C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr9:134048316..134050600;chr9:134050376..134050575 26863196 MeRIP-seq:(Medium) rs750040035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_847282,Human_RBP_ID_17437271,Human_RBP_ID_18963218 Human_Splice_Rec_1096833,Human_Splice_Rec_1096861,Human_Splice_Rec_1096871 Human_miRNA_ID_2386762,Human_miRNA_ID_2388237,Human_miRNA_ID_2399389,Human_miRNA_ID_2684425,Human_miRNA_ID_3030440 RMVar_hsa_circ_54565,RMVar_hsa_circ_81050,RMVar_hsa_circ_260697,RMVar_hsa_circ_260698,RMVar_hsa_circ_373881 107736 RMVar_ID_107736 Human_SNP_ID_417434713 m1A Human chr9 + 134050450 134050450 134050450 TGGCAGGAGGAGGTGGGGCGGCAGCTGGGGGGACTGGGACCGACGTGACGTTTGCAGTGATGGTT TGGCAGGAGGAGGTGGGGCGGCAGCTGGGGGGGCTGGGACCGACGTGACGTTTGCAGTGATGGTT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:134050320..134050600 26863196 MeRIP-seq:(Medium) rs754542391 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 107737 RMVar_ID_107737 Human_SNP_ID_417435954 m1A Human chr9 - 134053497 134053497 134053497 CAGGGCCTCTCCAAGCCGCTGCTGTGACAGAAAGTGAGTGAGCTGCCGGAGGATGTCCACCGCCA CAGGGCCTCTCCAAGCCGCTGCTGTGACAGAACGTGAGTGAGCTGCCGGAGGATGTCCACCGCCA T G BRD3 Ensembl:ENSG00000169925 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:134053323..134053600;chr9:134053314..134053608 26863196 MeRIP-seq:(Medium) rs764837695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1703233,Human_RBP_ID_5036558 Human_Splice_Rec_1096826,Human_Splice_Rec_1096854,Human_Splice_Rec_1096874,Human_Splice_Rec_1096878 RMVar_hsa_circ_54565,RMVar_hsa_circ_81050,RMVar_hsa_circ_260697,RMVar_hsa_circ_260698,RMVar_hsa_circ_373881,RMVar_hsa_circ_260699,RMVar_hsa_circ_333612 107738 RMVar_ID_107738 Human_SNP_ID_417438676 m1A Human chr9 - 134062313 134062313 134062313 CATGCCCCAGGATAGCCCCACCAGTCTGCTGAAGCGCCCCGGGACAGGGCTGGGCCTGTAGAGCC CATGCCCCAGGATAGCCCCACCAGTCTGCTGACGCGCCCCGGGACAGGGCTGGGCCTGTAGAGCC T G BRD3 Ensembl:ENSG00000169925 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134062304..134062651 26863196 MeRIP-seq:(Medium) rs1430537082 Functional Loss SNV dbSNP153 33..33 33 - - - 107739 RMVar_ID_107739 Human_SNP_ID_417438699 m1A Human chr9 - 134062386 134062386 134062386 GAACTGTGGGGTGCAGGGGACAGTCACGGGAGAGGCAGCGCTGGCAGCTGCACCTGCCCAGCGTG GAACTGTGGGGTGCAGGGGACAGTCACGGGAGCGGCAGCGCTGGCAGCTGCACCTGCCCAGCGTG T G BRD3 Ensembl:ENSG00000169925 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134062384..134062666 26863196 MeRIP-seq:(Medium) rs1349968463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3907714,Human_RBP_ID_5330134,Human_RBP_ID_8159417,Human_RBP_ID_8223869,Human_RBP_ID_22733125,Human_RBP_ID_26796240 107740 RMVar_ID_107740 Human_SNP_ID_417440369 m1A Human chr9 - 134067308 134067308 134067308 TCGGCCCTGGGCTCTGCGCGGCCTCCTCCCAGAGTTACGGGCCCAGAGCTGACTTTGAGCCCCCC TCGGCCCTGGGCTCTGCGCGGCCTCCTCCCAGGGTTACGGGCCCAGAGCTGACTTTGAGCCCCCC T C BRD3 Ensembl:ENSG00000169925 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134067305..134067477 26863196 MeRIP-seq:(Medium) rs1447991025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8731174,Human_RBP_ID_18467539,Human_RBP_ID_22484432 107741 RMVar_ID_107741 Human_SNP_ID_417440722 m1A Human chr9 - 134067974 134067974 134067974 GAGCCAAAGAGGAGCCGGCCGCGCGGGCCGGGAGGGGACGGCCGCCGGAGCCGCGAGGCCAAGTA GAGCCAAAGAGGAGCCGGCCGCGCGGGCCGGGCGGGGACGGCCGCCGGAGCCGCGAGGCCAAGTA T G BRD3 Ensembl:ENSG00000169925 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134067883..134068025 26863196 MeRIP-seq:(Medium) rs1161765499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5035973,Human_RBP_ID_9408832,Human_RBP_ID_18427522 Human_Splice_Rec_1096825 107742 RMVar_ID_107742 Human_SNP_ID_417440917 m1A Human chr9 + 134068398 134068398 134068398 GCCCCAGGACGGCATGGAAGAAGCGGGCACGCAGCCAGCACCGCAGCCCCCGTCCGGGCACCCCG GCCCCAGGACGGCATGGAAGAAGCGGGCACGCGGCCAGCACCGCAGCCCCCGTCCGGGCACCCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134068359..134068491 26863196 MeRIP-seq:(Medium) rs992943938 Functional Loss SNV dbSNP153 33..33 33 - - - 107743 RMVar_ID_107743 Human_SNP_ID_417459836 m1A Human chr9 + 134135573 134135573 134135573 GAACGCGCAGGTTCCTGGTCTTCCAGATGGGCAGGAATCGTCCTGCCCGCCCGGGGTGGGAGGCC GAACGCGCAGGTTCCTGGTCTTCCAGATGGGCGGGAATCGTCCTGCCCGCCCGGGGTGGGAGGCC A G WDR5 Ensembl:ENSG00000196363 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134135382..134135577 26863196 MeRIP-seq:(Medium) rs746354116 Functional Loss SNV dbSNP153 33..33 33 - - - 107744 RMVar_ID_107744 Human_SNP_ID_417459837 m1A Human chr9 + 134135573 134135573 134135573 GAACGCGCAGGTTCCTGGTCTTCCAGATGGGCAGGAATCGTCCTGCCCGCCCGGGGTGGGAGGCC GAACGCGCAGGTTCCTGGTCTTCCAGATGGGCTGGAATCGTCCTGCCCGCCCGGGGTGGGAGGCC A T WDR5 Ensembl:ENSG00000196363 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134135382..134135577 26863196 MeRIP-seq:(Medium) rs746354116 Functional Loss SNV dbSNP153 33..33 33 - - - 107745 RMVar_ID_107745 Human_SNP_ID_417459876 m1A Human chr9 + 134135711 134135711 134135711 CGATGATCAAGAAGGGGCCTGGTCGCCCGGGGAGGTGCCCCGGCCCGAATCGACTCCGGAGACAA CGATGATCAAGAAGGGGCCTGGTCGCCCGGGGCGGTGCCCCGGCCCGAATCGACTCCGGAGACAA A C WDR5 Ensembl:ENSG00000196363 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134135674..134135772 26863196 MeRIP-seq:(Medium) rs1346708670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1096892 107746 RMVar_ID_107746 Human_SNP_ID_417459877 m1A Human chr9 + 134135711 134135711 134135711 CGATGATCAAGAAGGGGCCTGGTCGCCCGGGGAGGTGCCCCGGCCCGAATCGACTCCGGAGACAA CGATGATCAAGAAGGGGCCTGGTCGCCCGGGGTGGTGCCCCGGCCCGAATCGACTCCGGAGACAA A T WDR5 Ensembl:ENSG00000196363 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134135674..134135772 26863196 MeRIP-seq:(Medium) rs1346708670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1096892 107747 RMVar_ID_107747 Human_SNP_ID_417460074 m1A Human chr9 + 134136170 134136170 134136170 CCCGCCCAGGCGGCGGCCGACGCGACGCCCCGAGCGCCCGGCCCCGCCGCCGCGGCCCGGCAGGT CCCGCCCAGGCGGCGGCCGACGCGACGCCCCGGGCGCCCGGCCCCGCCGCCGCGGCCCGGCAGGT A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr9:134136126..134136298;chr9:134136136..134136267 26863196 MeRIP-seq:(Medium) rs1246097026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5018065,Human_RBP_ID_5410370,Human_RBP_ID_18427523 Human_Splice_Rec_1096901 107748 RMVar_ID_107748 Human_SNP_ID_417461027 m1A Human chr9 + 134138699 134138699 134138699 GCCACACCTGTTCTCTGCAAAGTGGGTGTTGTAATTTCTCTGCCTTCCTCTTGGATGAAGACTTT GCCACACCTGTTCTCTGCAAAGTGGGTGTTGTTATTTCTCTGCCTTCCTCTTGGATGAAGACTTT A T WDR5 Ensembl:ENSG00000196363 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35401074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3193677,Human_RBP_ID_10422223 107749 RMVar_ID_107749 Human_SNP_ID_417461382 m1A Human chr9 + 134139929 134139929 134139929 AGCCCGAGACCGAGGCCGCCAGAGCACAGCCAACCCCTTCGTCATCCGCCACTCAGAGCAAGGTG AGCCCGAGACCGAGGCCGCCAGAGCACAGCCACCCCCTTCGTCATCCGCCACTCAGAGCAAGGTG A C WDR5 Ensembl:ENSG00000196363 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134139774..134139975 26863196 MeRIP-seq:(Medium) rs996722012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9407748,Human_RBP_ID_18472826 Human_Splice_Rec_1096889,Human_Splice_Rec_1096895,Human_Splice_Rec_1096903 Human_miRNA_ID_2384528,Human_miRNA_ID_2384529 RMVar_hsa_circ_47471,RMVar_hsa_circ_278837,RMVar_hsa_circ_86172,RMVar_hsa_circ_310348,RMVar_hsa_circ_260700,RMVar_hsa_circ_279062,RMVar_hsa_circ_89421,RMVar_hsa_circ_274086,RMVar_hsa_circ_48044,RMVar_hsa_circ_260701,RMVar_hsa_circ_9170,RMVar_hsa_circ_260702 107750 RMVar_ID_107750 Human_SNP_ID_417464188 m1A Human chr9 - 134149186 134149186 134149186 CCCGTCTTCTCAAGACCGATGGGGGGTCATGCATGGCGACTACAGACTGTGACCCCCTGGGGATC CCCGTCTTCTCAAGACCGATGGGGGGTCATGCGTGGCGACTACAGACTGTGACCCCCTGGGGATC T C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134149180..134149310 26863196 MeRIP-seq:(Medium) rs147334285 Functional Loss SNV dbSNP153 33..33 33 - - - 107751 RMVar_ID_107751 Human_SNP_ID_417465049 m1A Human chr9 + 134152456 134152456 134152456 AGGTGGATGGAGGTGTCCTGGGGGCACGGAGGACAGGCCTGAGGAGAGGAAGGAGGGACGTGGCG AGGTGGATGGAGGTGTCCTGGGGGCACGGAGGGCAGGCCTGAGGAGAGGAAGGAGGGACGTGGCG A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134152449..134152667 26863196 MeRIP-seq:(Medium) rs909884396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3909493 RMVar_hsa_circ_274086,RMVar_hsa_circ_9170,RMVar_hsa_circ_36157,RMVar_hsa_circ_104421,RMVar_hsa_circ_303693,RMVar_hsa_circ_260704,RMVar_hsa_circ_260707,RMVar_hsa_circ_260708,RMVar_hsa_circ_115590,RMVar_hsa_circ_376089,RMVar_hsa_circ_260709 107752 RMVar_ID_107752 Human_SNP_ID_417465062 m1A Human chr9 - 134152514 134152514 134152514 GCCGTCACAGACCCTCAGGCCACACCCTGCCCAGCACCTGGCCTTCCCATCCAGGCCACGCCACG GCCGTCACAGACCCTCAGGCCACACCCTGCCCGGCACCTGGCCTTCCCATCCAGGCCACGCCACG T C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134152504..134152619 26863196 MeRIP-seq:(Medium) rs918439908 Functional Loss SNV dbSNP153 33..33 33 - - - 107753 RMVar_ID_107753 Human_SNP_ID_417514150 m1A Human chr9 - 134326266 134326266 134326266 GGCCCGCGCCCCGCCCGCCCAGCCCCGCCCGGAGCGCGCCCCCCTCCGCCGCCGCCGCCCCGCGA GGCCCGCGCCCCGCCCGCCCAGCCCCGCCCGGGGCGCGCCCCCCTCCGCCGCCGCCGCCCCGCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134326217..134326289 26863196 MeRIP-seq:(Medium) rs1554745996 Functional Loss SNV dbSNP153 33..33 33 - - - 107754 RMVar_ID_107754 Human_SNP_ID_417516015 m1A Human chr9 + 134332554 134332554 134332554 GAGGGGTGGGGGAGGGGTGCCCAGAGGTAGGGACAGCAAGGTCTGGCCTGGAGGGGGTGAAGAGG GAGGGGTGGGGGAGGGGTGCCCAGAGGTAGGGTCAGCAAGGTCTGGCCTGGAGGGGGTGAAGAGG A T RXRA Ensembl:ENSG00000186350 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134332549..134332723 26863196 MeRIP-seq:(Medium) rs1427350607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5229308,Human_RBP_ID_8160195,Human_RBP_ID_8223894,Human_RBP_ID_18468011,Human_RBP_ID_18962503 RMVar_hsa_circ_107312,RMVar_hsa_circ_260711 107755 RMVar_ID_107755 Human_SNP_ID_417521602 m1A Human chr9 - 134351819 134351819 134351819 TGGCCTCCATAAATCTCTCCGAGGCCCCGCACACCCGCCTCTGATCAACCCAACTCCATGTCATT TGGCCTCCATAAATCTCTCCGAGGCCCCGCACGCCCGCCTCTGATCAACCCAACTCCATGTCATT T C lnc-BRD3-7 RNACentral:URS00008BDA03 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134351813..134352073 26863196 MeRIP-seq:(Medium) rs1444379042 Functional Loss SNV dbSNP153 33..33 33 - - - 107756 RMVar_ID_107756 Human_SNP_ID_417521603 m1A Human chr9 - 134351819 134351819 134351819 TGGCCTCCATAAATCTCTCCGAGGCCCCGCACACCCGCCTCTGATCAACCCAACTCCATGTCATT TGGCCTCCATAAATCTCTCCGAGGCCCCGCACCCCCGCCTCTGATCAACCCAACTCCATGTCATT T G lnc-BRD3-7 RNACentral:URS00008BDA03 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134351813..134352073 26863196 MeRIP-seq:(Medium) rs1444379042 Functional Loss SNV dbSNP153 33..33 33 - - - 107757 RMVar_ID_107757 Human_SNP_ID_417521604 m1A Human chr9 - 134351821 134351821 134351821 CGTGGCCTCCATAAATCTCTCCGAGGCCCCGCACACCCGCCTCTGATCAACCCAACTCCATGTCA CGTGGCCTCCATAAATCTCTCCGAGGCCCCGCGCACCCGCCTCTGATCAACCCAACTCCATGTCA T C lnc-BRD3-7 RNACentral:URS00008BDA03 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134351817..134352273 26863196 MeRIP-seq:(Medium) rs1383994568 Functional Loss SNV dbSNP153 33..33 33 - - - 107758 RMVar_ID_107758 Human_SNP_ID_417526707 m1A Human chr9 - 134369294 134369293 134369295 CACACACACAACCCCTGCACTCACACACACATAACCCCCACACACACACATAACCCCCCACACAC CACACACACAACCCCTGCACTCACACACACA__ACCCCCACACACACACATAACCCCCCACACAC TTA T lnc-BRD3-7 RNACentral:URS00008BDA03 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134369290..134369385 26863196 MeRIP-seq:(Medium) rs1214394916 Functional Loss DEL dbSNP153 32..33 33 - - - 107759 RMVar_ID_107759 Human_SNP_ID_417527185 m1A Human chr9 + 134370782 134370782 134370782 TGGCGGCGCCGGGTGGGCCTTGTGCACAGCCCAGCTCAGACCACGGAGGGTCTGGGGTTGGAGGT TGGCGGCGCCGGGTGGGCCTTGTGCACAGCCCCGCTCAGACCACGGAGGGTCTGGGGTTGGAGGT A C RXRA Ensembl:ENSG00000186350 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:134370777..134370889 32194978 MeRIP-seq:(Medium) rs1168146557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22628780 RMVar_hsa_circ_107312,RMVar_hsa_circ_260711 107760 RMVar_ID_107760 Human_SNP_ID_417527696 m1A Human chr9 + 134372523 134372523 134372523 GAATTGATTTGTTATCACTGGGTTCCAGGCACACGGCTTAGAGGGCATCACGGAGGCCTCCCCGT GAATTGATTTGTTATCACTGGGTTCCAGGCACGCGGCTTAGAGGGCATCACGGAGGCCTCCCCGT A G RXRA Ensembl:ENSG00000186350 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134372521..134372586 26863196 MeRIP-seq:(Medium) rs1006088228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107312,RMVar_hsa_circ_260711 107761 RMVar_ID_107761 Human_SNP_ID_417530131 m1A Human chr9 + 134380427 134380427 134380427 TCGCCTGGGGTCGGATAGGGGCTGGGGTGGCCATGAGAAGTGAGGAGCCTCCCATGACCCAGTGG TCGCCTGGGGTCGGATAGGGGCTGGGGTGGCCCTGAGAAGTGAGGAGCCTCCCATGACCCAGTGG A C RXRA Ensembl:ENSG00000186350 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134380389..134380490 26863196 MeRIP-seq:(Medium) rs1465478795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3908064,Human_RBP_ID_8159578,Human_RBP_ID_8224106,Human_RBP_ID_18962524 RMVar_hsa_circ_107312,RMVar_hsa_circ_260711 107762 RMVar_ID_107762 Human_SNP_ID_417536393 m1A Human chr9 - 134401769 134401769 134401769 CGAGAAAGGCGGGCCCATGCCGTTGATGGGGGAGCTCAGGGTGCTGATGGGAGAATGCAGCTGTC CGAGAAAGGCGGGCCCATGCCGTTGATGGGGGGGCTCAGGGTGCTGATGGGAGAATGCAGCTGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134401670..134401800 26863196 MeRIP-seq:(Medium) rs1253406380 Functional Loss SNV dbSNP153 33..33 33 - - - 107763 RMVar_ID_107763 Human_SNP_ID_417536401 m1A Human chr9 + 134401784 134401784 134401784 CCATCAGCACCCTGAGCTCCCCCATCAACGGCATGGGCCCGCCTTTCTCGGTCATCAGCTCCCCC CCATCAGCACCCTGAGCTCCCCCATCAACGGCGTGGGCCCGCCTTTCTCGGTCATCAGCTCCCCC A G RXRA Ensembl:ENSG00000186350 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134401733..134401834 26863196 MeRIP-seq:(Medium) rs201700387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5018214,Human_RBP_ID_17323655,Human_RBP_ID_17437408,Human_RBP_ID_18197017 Human_Splice_Rec_1096935,Human_Splice_Rec_1096957,Human_Splice_Rec_1096975 RMVar_hsa_circ_107312,RMVar_hsa_circ_63676,RMVar_hsa_circ_341322,RMVar_hsa_circ_260711,RMVar_hsa_circ_309807,RMVar_hsa_circ_260712 107764 RMVar_ID_107764 Human_SNP_ID_417536402 m1A Human chr9 - 134401785 134401785 134401785 TGGGGGAGCTGATGACCGAGAAAGGCGGGCCCATGCCGTTGATGGGGGAGCTCAGGGTGCTGATG TGGGGGAGCTGATGACCGAGAAAGGCGGGCCCGTGCCGTTGATGGGGGAGCTCAGGGTGCTGATG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134401736..134401835 26863196 MeRIP-seq:(Medium) rs552212769 Functional Loss SNV dbSNP153 33..33 33 - - - 107765 RMVar_ID_107765 Human_SNP_ID_417542484 m1A Human chr9 + 134421628 134421627 134421629 GCAGGGCCTGGTCTGGGCTGTGTTTGGTCAGTACACTGGCTTCTGGGACTGAATGTCCTGCTCTT GCAGGGCCTGGTCTGGGCTGTGTTTGGTCAGT__ACTGGCTTCTGGGACTGAATGTCCTGCTCTT TAC T RXRA Ensembl:ENSG00000186350 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134421623..134421832 26863196 MeRIP-seq:(Medium) rs777140941 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22690521 RMVar_hsa_circ_8239,RMVar_hsa_circ_341322,RMVar_hsa_circ_260712,RMVar_hsa_circ_352316,RMVar_hsa_circ_59680,RMVar_hsa_circ_267229,RMVar_hsa_circ_351416,RMVar_hsa_circ_354156,RMVar_hsa_circ_260715 107766 RMVar_ID_107766 Human_SNP_ID_417598671 m1A Human chr9 - 134622472 134622472 134622472 GCAGGGAGGAAGGCAGGGGGGAAGGGGCAAGAAAGGAAGGAGGAAAGGAATGGGAGAAGGAGGAA GCAGGGAGGAAGGCAGGGGGGAAGGGGCAAGACAGGAAGGAGGAAAGGAATGGGAGAAGGAGGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134622469..134622597 26863196 MeRIP-seq:(Medium) rs1334773081 Functional Loss SNV dbSNP153 33..33 33 - - - 107767 RMVar_ID_107767 Human_SNP_ID_417598723 m1A Human chr9 - 134622568 134622568 134622568 GGGATGGAGGCAGGGAGGAAGGCAGGGAGAGAAGGGCAGACAGAGGAGGGAAAGAGAAGAGAAAG GGGATGGAGGCAGGGAGGAAGGCAGGGAGAGAGGGGCAGACAGAGGAGGGAAAGAGAAGAGAAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134622275..134622615 26863196 MeRIP-seq:(Medium) rs4993044 Functional Loss SNV dbSNP153 33..33 33 - - - 107768 RMVar_ID_107768 Human_SNP_ID_417606810 m1A Human chr9 + 134652173 134652173 134652173 TGACTGCGATTGTAAGAGCTTTCTAGGTAATTATTATTCATGCTATTTAGGGTCATAGGTCTCAG TGACTGCGATTGTAAGAGCTTTCTAGGTAATTGTTATTCATGCTATTTAGGGTCATAGGTCTCAG A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134652170..134652263 26863196 MeRIP-seq:(Medium) rs1262229899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98505,RMVar_hsa_circ_260716 107769 RMVar_ID_107769 Human_SNP_ID_417607940 m1A Human chr9 + 134654965 134654965 134654965 AGGGCTGGGGGTGTGTAGAGCTGGGGGAGGGTAGGGCTGGTGTGTGTAGGGCTGGAGGTGTGTAG AGGGCTGGGGGTGTGTAGAGCTGGGGGAGGGTGGGGCTGGTGTGTGTAGGGCTGGAGGTGTGTAG A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:134654962..134655190 26863196 MeRIP-seq:(Medium) rs1468000791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5227379 RMVar_hsa_circ_98505,RMVar_hsa_circ_260716 107770 RMVar_ID_107770 Human_SNP_ID_417609029 m1A Human chr9 + 134657778 134657778 134657778 CAGGCCTGACGGGGAAGGGCAGGGGGTGGGACAGGACCTGCCTGGACTCCTGGAGAGGACTCTGA CAGGCCTGACGGGGAAGGGCAGGGGGTGGGACGGGACCTGCCTGGACTCCTGGAGAGGACTCTGA A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134657772..134657980 26863196 MeRIP-seq:(Medium) rs1349808220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98505,RMVar_hsa_circ_260716 107771 RMVar_ID_107771 Human_SNP_ID_417611519 m1A Human chr9 - 134668366 134668366 134668366 GGCGTTTGCACATTCTGTTCCTCAGACCTGGAATCCTCCTCTTCCCCCGACTCCCACTCTTGGTG GGCGTTTGCACATTCTGTTCCTCAGACCTGGAGTCCTCCTCTTCCCCCGACTCCCACTCTTGGTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134668364..134668477 26863196 MeRIP-seq:(Medium) rs1310525477 Functional Loss SNV dbSNP153 33..33 33 - - - 107772 RMVar_ID_107772 Human_SNP_ID_417614634 m1A Human chr9 - 134680650 134680650 134680650 TTAGAACAGCGCTCCCTGGGGTTGTGCAGTGCACAGCATGGCCACCCTCCCCAAGCCCCTGGGGC TTAGAACAGCGCTCCCTGGGGTTGTGCAGTGCTCAGCATGGCCACCCTCCCCAAGCCCCTGGGGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134680646..134680729 26863196 MeRIP-seq:(Medium) rs747459555 Functional Loss SNV dbSNP153 33..33 33 - - - 107773 RMVar_ID_107773 Human_SNP_ID_417615161 m1A Human chr9 + 134682564 134682564 134682564 GAATCCTACCACACTGCCTGGTGGGGTGGGGGAGAGCCTGCTGCCCAGGAAGGGCGCAGGAATCC GAATCCTACCACACTGCCTGGTGGGGTGGGGGGGAGCCTGCTGCCCAGGAAGGGCGCAGGAATCC A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134682555..134682760 26863196 MeRIP-seq:(Medium) rs992841768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98505,RMVar_hsa_circ_260716 107774 RMVar_ID_107774 Human_SNP_ID_417616212 m1A Human chr9 - 134685565 134685561 134685565 TGGATGGATGGAGGATGGATGGATGGATGAATAGATGGATGGATGGATGCTGGATGGATGGATGG TGGATGGATGGAGGATGGATGGATGGATGAAT____GGATGGATGGATGCTGGATGGATGGATGG CATCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134685557..134685641 26863196 MeRIP-seq:(Medium) rs1454874647 Functional Loss DEL dbSNP153 33..36 33 - - - 107775 RMVar_ID_107775 Human_SNP_ID_417616214 m1A Human chr9 - 134685565 134685565 134685565 TGGATGGATGGAGGATGGATGGATGGATGAATAGATGGATGGATGGATGCTGGATGGATGGATGG TGGATGGATGGAGGATGGATGGATGGATGAATGGATGGATGGATGGATGCTGGATGGATGGATGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134685557..134685641 26863196 MeRIP-seq:(Medium) rs1264902450 Functional Loss SNV dbSNP153 33..33 33 - - - 107776 RMVar_ID_107776 Human_SNP_ID_417617781 m1A Human chr9 + 134691000 134691000 134691000 ACAAAGACAACAGGCTTTTGCGCCACGCGGCGATCTTCCAAAGGCCCGGATGTCGCTTACAGAGT ACAAAGACAACAGGCTTTTGCGCCACGCGGCGCTCTTCCAAAGGCCCGGATGTCGCTTACAGAGT A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134690809..134691117 26863196 MeRIP-seq:(Medium) rs1463204835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633888 Human_Splice_Rec_1097002,Human_Splice_Rec_1097003,Human_Splice_Rec_1097132,Human_Splice_Rec_1097133,Human_Splice_Rec_1097262 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_98505,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_310012,RMVar_hsa_circ_260716,RMVar_hsa_circ_297831,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260728,RMVar_hsa_circ_43159,RMVar_hsa_circ_260729,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_260717 107777 RMVar_ID_107777 Human_SNP_ID_417623674 m1A Human chr9 + 134710913 134710913 134710913 GGAGCCCTATTTGTTGGGTGCAGTGGTGGGGGAGGGGCCCCGTCTGTTGGGTGCAGTGGTGGGGG GGAGCCCTATTTGTTGGGTGCAGTGGTGGGGGGGGGGCCCCGTCTGTTGGGTGCAGTGGTGGGGG A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:134710911..134711040 26863196 MeRIP-seq:(Medium) rs1371054552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731 107778 RMVar_ID_107778 Human_SNP_ID_417624609 m1A Human chr9 + 134713815 134713815 134713815 AAACTGTGCTGAACAGAAGCTGAATAGAAAGAACTGGGGTCTGAACCCGGGACAGAGAAGGTGGG AAACTGTGCTGAACAGAAGCTGAATAGAAAGACCTGGGGTCTGAACCCGGGACAGAGAAGGTGGG A C COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134713812..134713939 26863196 MeRIP-seq:(Medium) rs1016798689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731 107779 RMVar_ID_107779 Human_SNP_ID_417628932 m1A Human chr9 + 134728734 134728734 134728734 TTACTACGAATACCCCTACTACGAAGACCCCGAAGACCTAGGGAAGGAGCCCACCCCCAGCAAGA TTACTACGAATACCCCTACTACGAAGACCCCGGAGACCTAGGGAAGGAGCCCACCCCCAGCAAGA A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134728622..134728961 26863196 MeRIP-seq:(Medium) rs750381860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097010,Human_Splice_Rec_1097011,Human_Splice_Rec_1097140,Human_Splice_Rec_1097141 Human_miRNA_ID_1706354 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_313301,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742 107780 RMVar_ID_107780 Human_SNP_ID_417629436 m1A Human chr9 + 134730187 134730178 134730187 CCGGACATGCGGCAAGTCCCAGACCTGGCACCACTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC CCGGACATGCGGCAAGTCCCAGAC_________CTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC CCTGGCACCA C COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134730184..134730520 26863196 MeRIP-seq:(Medium) rs1273748389 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742 107781 RMVar_ID_107781 Human_SNP_ID_417629442 m1A Human chr9 + 134730187 134730187 134730187 CCGGACATGCGGCAAGTCCCAGACCTGGCACCACTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC CCGGACATGCGGCAAGTCCCAGACCTGGCACCGCTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134730184..134730520 26863196 MeRIP-seq:(Medium) rs3124308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742 107782 RMVar_ID_107782 Human_SNP_ID_417629464 m1A Human chr9 - 134730230 134730230 134730230 AGCTTCCGTGGGGGTCGGGGTCAGCTCCTGGGAGCCAAGGACAGAGACAGCTGGAGTCAGGGCGG AGCTTCCGTGGGGGTCGGGGTCAGCTCCTGGGGGCCAAGGACAGAGACAGCTGGAGTCAGGGCGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:134730226..134730275 26863196 MeRIP-seq:(Medium) rs762522930 Functional Loss SNV dbSNP153 33..33 33 - - - 107783 RMVar_ID_107783 Human_SNP_ID_417629542 m1A Human chr9 + 134730399 134730399 134730399 TGATGACCTCACCTATGGCGAGGGGGAGGAGAACCCCGACCAGCCCACAGACCCAGGCGCTGGGG TGATGACCTCACCTATGGCGAGGGGGAGGAGACCCCCGACCAGCCCACAGACCCAGGCGCTGGGG A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:134730351..134732100 26863196 MeRIP-seq:(Medium) rs1026084450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097013,Human_Splice_Rec_1097143 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742,RMVar_hsa_circ_21764,RMVar_hsa_circ_285353 107784 RMVar_ID_107784 Human_SNP_ID_417629552 m1A Human chr9 + 134730413 134730413 134730413 ATGGCGAGGGGGAGGAGAACCCCGACCAGCCCACAGACCCAGGCGCTGGGGCCGAAATTCCCACC ATGGCGAGGGGGAGGAGAACCCCGACCAGCCCCCAGACCCAGGCGCTGGGGCCGAAATTCCCACC A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134730190..134730518 26863196 MeRIP-seq:(Medium) rs766771487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097013,Human_Splice_Rec_1097143 Human_miRNA_ID_475555 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742,RMVar_hsa_circ_21764,RMVar_hsa_circ_285353 107785 RMVar_ID_107785 Human_SNP_ID_417629553 m1A Human chr9 + 134730413 134730413 134730413 ATGGCGAGGGGGAGGAGAACCCCGACCAGCCCACAGACCCAGGCGCTGGGGCCGAAATTCCCACC ATGGCGAGGGGGAGGAGAACCCCGACCAGCCCTCAGACCCAGGCGCTGGGGCCGAAATTCCCACC A T COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134730190..134730518 26863196 MeRIP-seq:(Medium) rs766771487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097013,Human_Splice_Rec_1097143 Human_miRNA_ID_475555 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742,RMVar_hsa_circ_21764,RMVar_hsa_circ_285353 107786 RMVar_ID_107786 Human_SNP_ID_417629925 m1A Human chr9 + 134731572 134731572 134731572 GTTCACTGAGGAAACGATCCGGAACCTTGACGAGAACTACTACGACCCCTACTACGACCCCACCA GTTCACTGAGGAAACGATCCGGAACCTTGACGGGAACTACTACGACCCCTACTACGACCCCACCA A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134731434..134731723 26863196 MeRIP-seq:(Medium) rs768952767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637103 Human_Splice_Rec_1097014,Human_Splice_Rec_1097015,Human_Splice_Rec_1097144,Human_Splice_Rec_1097145,Human_Splice_Rec_1097269 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742,RMVar_hsa_circ_21764,RMVar_hsa_circ_26161,RMVar_hsa_circ_34999,RMVar_hsa_circ_53325,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_80233,RMVar_hsa_circ_43821,RMVar_hsa_circ_31088,RMVar_hsa_circ_4525,RMVar_hsa_circ_16104,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_260746 107787 RMVar_ID_107787 Human_SNP_ID_417631898 m1A Human chr9 - 134738457 134738455 134738457 CCTCGATGAGCATGCCCTGGGGAGACAGAGAGAGGGCGTCTGAGACCGCAGCCCATCCCTCCCGA CCTCGATGAGCATGCCCTGGGGAGACAGAGAG__GGCGTCTGAGACCGCAGCCCATCCCTCCCGA CCT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134738451..134738500 26863196 MeRIP-seq:(Medium) rs863223441 Functional Loss DEL dbSNP153 33..34 33 - - - 107788 RMVar_ID_107788 Human_SNP_ID_417631901 m1A Human chr9 - 134738457 134738457 134738457 CCTCGATGAGCATGCCCTGGGGAGACAGAGAGAGGGCGTCTGAGACCGCAGCCCATCCCTCCCGA CCTCGATGAGCATGCCCTGGGGAGACAGAGAGGGGGCGTCTGAGACCGCAGCCCATCCCTCCCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134738451..134738500 26863196 MeRIP-seq:(Medium) rs767955467 Functional Loss SNV dbSNP153 33..33 33 - - - 107789 RMVar_ID_107789 Human_SNP_ID_417636997 m1A Human chr9 - 134753900 134753900 134753900 CAGACAGCGAAGGCAAGGATCCCACATACCTGAGGCCCCACGTCTCCCGGCTCGCCCTTCAAACC CAGACAGCGAAGGCAAGGATCCCACATACCTGGGGCCCCACGTCTCCCGGCTCGCCCTTCAAACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:134753810..134753955;chr9:134753876..134753925;chr9:134753851..134753925 26863196 MeRIP-seq:(Medium) rs112318669 Functional Loss SNV dbSNP153 33..33 33 - - - 107790 RMVar_ID_107790 Human_SNP_ID_417636998 m1A Human chr9 + 134753902 134753902 134753902 TTTGAAGGGCGAGCCGGGAGACGTGGGGCCTCAGGTATGTGGGATCCTTGCCTTCGCTGTCTGGT TTTGAAGGGCGAGCCGGGAGACGTGGGGCCTCCGGTATGTGGGATCCTTGCCTTCGCTGTCTGGT A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134753851..134753925 26863196 MeRIP-seq:(Medium) rs1243536977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097028,Human_Splice_Rec_1097029,Human_Splice_Rec_1097158,Human_Splice_Rec_1097159 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260742,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_43821,RMVar_hsa_circ_121881,RMVar_hsa_circ_16104,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818 107791 RMVar_ID_107791 Human_SNP_ID_417637115 m1A Human chr9 - 134754252 134754252 134754252 ACCTCGAGGACCCTGCCAGGGGTAAGAGACAAAGGGTCAGTGGCGAGTCCGCCTTTCTCAGGAGA ACCTCGAGGACCCTGCCAGGGGTAAGAGACAAGGGGTCAGTGGCGAGTCCGCCTTTCTCAGGAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134754251..134754350 26863196 MeRIP-seq:(Medium) rs754059459 Functional Loss SNV dbSNP153 33..33 33 - - - 107792 RMVar_ID_107792 Human_SNP_ID_417638199 m1A Human chr9 - 134758090 134758090 134758090 CCCTGAACCCCATCGGCCAGCCCTCTCCCCATAGGCCCCCACTTTGCATCTACAATCTCAGCCTC CCCTGAACCCCATCGGCCAGCCCTCTCCCCATCGGCCCCCACTTTGCATCTACAATCTCAGCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134758085..134758300 26863196 MeRIP-seq:(Medium) rs976201693 Functional Loss SNV dbSNP153 33..33 33 - - - 107793 RMVar_ID_107793 Human_SNP_ID_417639371 m1A Human chr9 + 134759913 134759911 134759913 CCACACAGGCACACACACACCCATGCACCCCCACACTCATACATGCACACACACGCATACATACC CCACACAGGCACACACACACCCATGCACCCC__CACTCATACATGCACACACACGCATACATACC CCA C COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134759911..134760176 26863196 MeRIP-seq:(Medium) rs573910644 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260742,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_121881,RMVar_hsa_circ_16104,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_268922,RMVar_hsa_circ_10954,RMVar_hsa_circ_86251,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_260750 107794 RMVar_ID_107794 Human_SNP_ID_417640938 m1A Human chr9 - 134761933 134761933 134761933 TCTCCCGGAGGTCCTGGTGGGCCGGAAGGACCAGGGTCACCCTAGGAAGTGAAAGGGTCAACGTC TCTCCCGGAGGTCCTGGTGGGCCGGAAGGACCGGGGTCACCCTAGGAAGTGAAAGGGTCAACGTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134761926..134761975 26863196 MeRIP-seq:(Medium) rs755661291 Functional Loss SNV dbSNP153 33..33 33 - - - 107795 RMVar_ID_107795 Human_SNP_ID_417640939 m1A Human chr9 - 134761933 134761933 134761933 TCTCCCGGAGGTCCTGGTGGGCCGGAAGGACCAGGGTCACCCTAGGAAGTGAAAGGGTCAACGTC TCTCCCGGAGGTCCTGGTGGGCCGGAAGGACCCGGGTCACCCTAGGAAGTGAAAGGGTCAACGTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134761926..134761975 26863196 MeRIP-seq:(Medium) rs755661291 Functional Loss SNV dbSNP153 33..33 33 - - - 107796 RMVar_ID_107796 Human_SNP_ID_417642159 m1A Human chr9 + 134765716 134765716 134765716 CCACGTGGTCTGCTTGGGCCGAAGGGGCCCCCAGGTCCTCCCGGACCTCCCGTAAGTCCCATTAC CCACGTGGTCTGCTTGGGCCGAAGGGGCCCCCGGGTCCTCCCGGACCTCCCGTAAGTCCCATTAC A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:134765676..134765750;chr9:134765676..134765725 26863196 MeRIP-seq:(Medium) rs1060504527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097040,Human_Splice_Rec_1097041,Human_Splice_Rec_1097170,Human_Splice_Rec_1097171 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_121881,RMVar_hsa_circ_16104,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_268922,RMVar_hsa_circ_10954,RMVar_hsa_circ_86251,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_260750,RMVar_hsa_circ_260751,RMVar_hsa_circ_110621 107797 RMVar_ID_107797 Human_SNP_ID_417642946 m1A Human chr9 + 134768436 134768436 134768436 TTCTAGGGTCCCTTGGGGAAACCAGGCCTTCCAGGAATGCCCGGTGCTGACGGACCCCCGGTGAG TTCTAGGGTCCCTTGGGGAAACCAGGCCTTCCGGGAATGCCCGGTGCTGACGGACCCCCGGTGAG A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:134738489..134806234 32194978 MeRIP-seq:(Medium) rs776416548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097048,Human_Splice_Rec_1097049,Human_Splice_Rec_1097178,Human_Splice_Rec_1097179 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_121881,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_268922,RMVar_hsa_circ_10954,RMVar_hsa_circ_86251,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_260750,RMVar_hsa_circ_260751,RMVar_hsa_circ_110621,RMVar_hsa_circ_266377 107798 RMVar_ID_107798 Human_SNP_ID_417644101 m1A Human chr9 - 134772779 134772779 134772779 GGCCTTCTTTGCCAGGGTGTCCCTGTCACAAAAGAAGAAGCATTGATTAGTCAGTGCCACTCCAG GGCCTTCTTTGCCAGGGTGTCCCTGTCACAAAGGAAGAAGCATTGATTAGTCAGTGCCACTCCAG T C AL645768.1 Ensembl:ENSG00000286502 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134772776..134772850 26863196 MeRIP-seq:(Medium) rs372326878 Functional Loss SNV dbSNP153 33..33 33 - - - 107799 RMVar_ID_107799 Human_SNP_ID_417645963 m1A Human chr9 + 134779776 134779776 134779776 CCTCTGAAAGGTGGGGGTGTTTCTAGAAGATGATGCTATAATGGGAAGCAGGAGGGGTGTGTTGG CCTCTGAAAGGTGGGGGTGTTTCTAGAAGATGGTGCTATAATGGGAAGCAGGAGGGGTGTGTTGG A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134779774..134779950 26863196 MeRIP-seq:(Medium) rs56309633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_86251,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_260750,RMVar_hsa_circ_266377,RMVar_hsa_circ_347559 107800 RMVar_ID_107800 Human_SNP_ID_417645964 m1A Human chr9 + 134779776 134779776 134779776 CCTCTGAAAGGTGGGGGTGTTTCTAGAAGATGATGCTATAATGGGAAGCAGGAGGGGTGTGTTGG CCTCTGAAAGGTGGGGGTGTTTCTAGAAGATGTTGCTATAATGGGAAGCAGGAGGGGTGTGTTGG A T COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134779774..134779950 26863196 MeRIP-seq:(Medium) rs56309633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_86251,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_260750,RMVar_hsa_circ_266377,RMVar_hsa_circ_347559 107801 RMVar_ID_107801 Human_SNP_ID_417646832 m1A Human chr9 + 134782614 134782614 134782614 GTGTGGTTGTTTGGAGCGGGGAAGGGACCGCCAGGGAGGCGGGTCCTCTTGCCTAGACTAGGGCA GTGTGGTTGTTTGGAGCGGGGAAGGGACCGCCGGGGAGGCGGGTCCTCTTGCCTAGACTAGGGCA A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134782608..134782764 26863196 MeRIP-seq:(Medium) rs552938159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_347559 107802 RMVar_ID_107802 Human_SNP_ID_417647488 m1A Human chr9 + 134784934 134784931 134784934 CCCCTTGCTCCTTGCTCTCAGAATGGTGGTGGAGAATAGTGTGTGTGCGGGGGGTGGTCTTCTCA CCCCTTGCTCCTTGCTCTCAGAATGGTGGT___GAATAGTGTGTGTGCGGGGGGTGGTCTTCTCA TGGA T COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134784931..134785132 26863196 MeRIP-seq:(Medium) rs772649334 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_78280,RMVar_hsa_circ_352542,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753 107803 RMVar_ID_107803 Human_SNP_ID_417647489 m1A Human chr9 + 134784934 134784934 134784934 CCCCTTGCTCCTTGCTCTCAGAATGGTGGTGGAGAATAGTGTGTGTGCGGGGGGTGGTCTTCTCA CCCCTTGCTCCTTGCTCTCAGAATGGTGGTGGTGAATAGTGTGTGTGCGGGGGGTGGTCTTCTCA A T COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134784931..134785132 26863196 MeRIP-seq:(Medium) rs540484447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_78280,RMVar_hsa_circ_352542,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753 107804 RMVar_ID_107804 Human_SNP_ID_417647618 m1A Human chr9 - 134785077 134785077 134785077 CCACATCACAAACCTTCTCCCCAGGGGGTCCCAGAGGACCGGGGTCACCATTGGGACCTCCGCGA CCACATCACAAACCTTCTCCCCAGGGGGTCCCGGAGGACCGGGGTCACCATTGGGACCTCCGCGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134785026..134785100 26863196 MeRIP-seq:(Medium) rs775092962 Functional Loss SNV dbSNP153 33..33 33 - - - 107805 RMVar_ID_107805 Human_SNP_ID_417648396 m1A Human chr9 - 134787897 134787897 134787897 GGCTTCAGCTCTAGAAAGCCAAATGGAGTTTCATCATGCTCCCTCCCCTGCCACCATCCCCCACG GGCTTCAGCTCTAGAAAGCCAAATGGAGTTTCGTCATGCTCCCTCCCCTGCCACCATCCCCCACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134787895..134788485 26863196 MeRIP-seq:(Medium) rs1564458833 Functional Loss SNV dbSNP153 33..33 33 - - - 107806 RMVar_ID_107806 Human_SNP_ID_417648473 m1A Human chr9 - 134788191 134788191 134788191 ACCCACCTACCCATTCATCGATTTGCCTACCTATAAACCCACCCCTCCATTCATCCACTTGTCTA ACCCACCTACCCATTCATCGATTTGCCTACCTGTAAACCCACCCCTCCATTCATCCACTTGTCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134788188..134788429 26863196 MeRIP-seq:(Medium) rs535909891 Functional Loss SNV dbSNP153 33..33 33 - - - 107807 RMVar_ID_107807 Human_SNP_ID_417648764 m1A Human chr9 - 134789033 134789033 134789033 TGCACAGCCTCTGCCCCAGACTCCACCTGCCCACCCACCCAACCACCCACCTACCTGTCTACCTA TGCACAGCCTCTGCCCCAGACTCCACCTGCCCCCCCACCCAACCACCCACCTACCTGTCTACCTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134789028..134789148 26863196 MeRIP-seq:(Medium) rs969819264 Functional Loss SNV dbSNP153 33..33 33 - - - 107808 RMVar_ID_107808 Human_SNP_ID_417649656 m1A Human chr9 + 134791941 134791941 134791941 ACTCAGAGGAGTGGTGGCTGTGATGATGAAGGACAAGGGTGAGTCAGGGAAAGGTCATAGGCACC ACTCAGAGGAGTGGTGGCTGTGATGATGAAGGTCAAGGGTGAGTCAGGGAAAGGTCATAGGCACC A T COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134791939..134792170 26863196 MeRIP-seq:(Medium) rs1441423172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_115455,RMVar_hsa_circ_260757,RMVar_hsa_circ_260758 107809 RMVar_ID_107809 Human_SNP_ID_417650733 m1A Human chr9 + 134795292 134795292 134795292 AGGGTCCGAGGGGTGAAAGAGGCCCCCGGGGCATCACTGGGAAGCCTGGCCCCAAGGTATGTTTT AGGGTCCGAGGGGTGAAAGAGGCCCCCGGGGCGTCACTGGGAAGCCTGGCCCCAAGGTATGTTTT A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134795076..134795300 26863196 MeRIP-seq:(Medium) rs1416663164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097066,Human_Splice_Rec_1097067,Human_Splice_Rec_1097196,Human_Splice_Rec_1097197 Human_miRNA_ID_2662137,Human_miRNA_ID_2680586 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_15415,RMVar_hsa_circ_115455,RMVar_hsa_circ_260757,RMVar_hsa_circ_115024,RMVar_hsa_circ_260758,RMVar_hsa_circ_260759 107810 RMVar_ID_107810 Human_SNP_ID_417651711 m1A Human chr9 + 134798452 134798452 134798452 AAGGATGGACTCCCAGGACACCCTGGACAGAGAGGCGAGACTGTGAGTATCGAGGGTGCTGGGGG AAGGATGGACTCCCAGGACACCCTGGACAGAGCGGCGAGACTGTGAGTATCGAGGGTGCTGGGGG A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:134798451..134798475 26863196 MeRIP-seq:(Medium) rs1400267883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097072,Human_Splice_Rec_1097073,Human_Splice_Rec_1097202,Human_Splice_Rec_1097203 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_15415,RMVar_hsa_circ_115455,RMVar_hsa_circ_260757,RMVar_hsa_circ_115024,RMVar_hsa_circ_260758,RMVar_hsa_circ_260759 107811 RMVar_ID_107811 Human_SNP_ID_417653649 m1A Human chr9 - 134805063 134805063 134805063 CATTTCATTCCCCGCCTGGCCTCTCACTCACCACTGGACCAGGAAGCCCTCGGTCCCCAGGGAAA CATTTCATTCCCCGCCTGGCCTCTCACTCACCCCTGGACCAGGAAGCCCTCGGTCCCCAGGGAAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:134805053..134805147;chr9:134805026..134805149 26863196 MeRIP-seq:(Medium) rs372109796 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_693 107812 RMVar_ID_107812 Human_SNP_ID_417653699 m1A Human chr9 + 134805177 134805177 134805177 TTTCATGGCTTTGCAGGGAGCTCTTGGACTGAAAGGCAATGAAGGGCCCCCTGGCCCACCAGGCC TTTCATGGCTTTGCAGGGAGCTCTTGGACTGACAGGCAATGAAGGGCCCCCTGGCCCACCAGGCC A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134804976..134805225 26863196 MeRIP-seq:(Medium) rs1304030944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097080,Human_Splice_Rec_1097081,Human_Splice_Rec_1097210,Human_Splice_Rec_1097211 RMVar_hsa_circ_85559,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_268922,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_260757,RMVar_hsa_circ_115024,RMVar_hsa_circ_108028,RMVar_hsa_circ_260759,RMVar_hsa_circ_260760 107813 RMVar_ID_107813 Human_SNP_ID_417654964 m1A Human chr9 + 134809284 134809284 134809284 GCTGGCCCTGTGGGTCCCCCTGGAGAAGACGGAGATAAGGTAAGGCAAATCCAGAGTGACCCATG GCTGGCCCTGTGGGTCCCCCTGGAGAAGACGGCGATAAGGTAAGGCAAATCCAGAGTGACCCATG A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr9:134809145..134809343;chr9:134809142..134809335;chr9:134809124..134809349;chr9:134809176..134809355;chr9:134809176..134809300 26863196 MeRIP-seq:(Medium) rs1296980747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097085,Human_Splice_Rec_1097215,Human_Splice_Rec_1097271 RMVar_hsa_circ_85559,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_83977,RMVar_hsa_circ_260745,RMVar_hsa_circ_268922,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_260757,RMVar_hsa_circ_115024,RMVar_hsa_circ_108028,RMVar_hsa_circ_260759,RMVar_hsa_circ_77013,RMVar_hsa_circ_260760,RMVar_hsa_circ_260761 107814 RMVar_ID_107814 Human_SNP_ID_417656471 m1A Human chr9 - 134813980 134813980 134813980 GCCAGGCTCACCTGCTTCGCCAGGCTCGCCCTAGGGAGACAGTGCATGTGGTTATGGCAGCGGTG GCCAGGCTCACCTGCTTCGCCAGGCTCGCCCTGGGGAGACAGTGCATGTGGTTATGGCAGCGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134813976..134814050 26863196 MeRIP-seq:(Medium) rs1465448974 Functional Loss SNV dbSNP153 33..33 33 - - - 107815 RMVar_ID_107815 Human_SNP_ID_417656752 m1A Human chr9 - 134814889 134814889 134814889 GTGTCTGGAATACTCACAGGGCTGCCTTTGGGACCATCATCTCCGGGAGGGCCTTTGGGTCCAGG GTGTCTGGAATACTCACAGGGCTGCCTTTGGGGCCATCATCTCCGGGAGGGCCTTTGGGTCCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134814839..134814945 26863196 MeRIP-seq:(Medium) rs1554805651 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_694 107816 RMVar_ID_107816 Human_SNP_ID_417656949 m1A Human chr9 + 134815614 134815614 134815614 GTGGGTTTTCCTGGAGATCCTGGCCCCCCCGGAGAGCCTGGCCCCGCGGTAGGTGCTCAAGAGGG GTGGGTTTTCCTGGAGATCCTGGCCCCCCCGGCGAGCCTGGCCCCGCGGTAGGTGCTCAAGAGGG A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134815576..134815625 26863196 MeRIP-seq:(Medium) rs1410328897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1097100,Human_Splice_Rec_1097101,Human_Splice_Rec_1097230,Human_Splice_Rec_1097231 Human_miRNA_ID_2662140,Human_miRNA_ID_2680589,Human_miRNA_ID_3065822 RMVar_hsa_circ_108153,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_77100,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_260735,RMVar_hsa_circ_83977,RMVar_hsa_circ_260745,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_99056,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_260753,RMVar_hsa_circ_260756,RMVar_hsa_circ_260757,RMVar_hsa_circ_108028,RMVar_hsa_circ_77013,RMVar_hsa_circ_260760,RMVar_hsa_circ_260761,RMVar_hsa_circ_101154,RMVar_hsa_circ_260762,RMVar_hsa_circ_260763 107817 RMVar_ID_107817 Human_SNP_ID_417658035 m1A Human chr9 - 134818762 134818762 134818762 GCAACCCCTCTGCCCCTCACAGCCTACTCACCACAGGGCCAGGGATCCCTCGAAGGCCATCCGGT GCAACCCCTCTGCCCCTCACAGCCTACTCACCCCAGGGCCAGGGATCCCTCGAAGGCCATCCGGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134818726..134818775 26863196 MeRIP-seq:(Medium) rs137862320 Functional Loss SNV dbSNP153 33..33 33 - - - 107818 RMVar_ID_107818 Human_SNP_ID_417660863 m1A Human chr9 - 134826723 134826722 134826723 CACACACCCGAACACCATGTACACACCCACACACCACCCACACACCCCCACATACCAGCCACACG CACACACCCGAACACCATGTACACACCCACAC_CCACCCACACACCCCCACATACCAGCCACACG GT G LOC101448202,LOC101448202:2,LOC101448202:3,LOC101448202:4,LOC101448202:5 RNACentral:URS0000D577CE,RNACentral:URS000075CC5B,RNACentral:URS0000D5A355,RNACentral:URS0000D5A859,RNACentral:URS0000D599F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr9:134826487..134826914;chr9:134826620..134826908 26863196 MeRIP-seq:(Medium) rs1302058518 Functional Loss DEL dbSNP153 33..33 33 - - - 107819 RMVar_ID_107819 Human_SNP_ID_417661478 m1A Human chr9 + 134828521 134828515 134828522 CAGGCCACACACCACACATACCACACAGATACACGATACACATACCACACACCACAGAGATACGC CAGGCCACACACCACACATACCACACA_______GATACACATACCACACACCACAGAGATACGC AGATACAC A COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134828518..134828632 26863196 MeRIP-seq:(Medium) rs1324600214 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_108153,RMVar_hsa_circ_260717,RMVar_hsa_circ_83977,RMVar_hsa_circ_260745,RMVar_hsa_circ_101154,RMVar_hsa_circ_260763,RMVar_hsa_circ_17295 107820 RMVar_ID_107820 Human_SNP_ID_417663891 m1A Human chr9 + 134835016 134835016 134835016 ACGCCGAGGGCAACCCTGTGGGTGTGGTACAGATGACCTTCCTGCGGCTGCTGAGCGCCTCTGCC ACGCCGAGGGCAACCCTGTGGGTGTGGTACAGGTGACCTTCCTGCGGCTGCTGAGCGCCTCTGCC A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134834972..134835241 26863196 MeRIP-seq:(Medium) rs138068984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27543847 Human_Splice_Rec_1097128,Human_Splice_Rec_1097258,Human_Splice_Rec_1097286 Human_miRNA_ID_1425080,Human_miRNA_ID_2727717 Clinvar_Rec_695 RMVar_hsa_circ_108153,RMVar_hsa_circ_260717,RMVar_hsa_circ_83977,RMVar_hsa_circ_260745,RMVar_hsa_circ_17295,RMVar_hsa_circ_52706 107821 RMVar_ID_107821 Human_SNP_ID_417663892 m1A Human chr9 + 134835016 134835016 134835016 ACGCCGAGGGCAACCCTGTGGGTGTGGTACAGATGACCTTCCTGCGGCTGCTGAGCGCCTCTGCC ACGCCGAGGGCAACCCTGTGGGTGTGGTACAGTTGACCTTCCTGCGGCTGCTGAGCGCCTCTGCC A T COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134834972..134835241 26863196 MeRIP-seq:(Medium) rs138068984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27543847 Human_Splice_Rec_1097128,Human_Splice_Rec_1097258,Human_Splice_Rec_1097286 Human_miRNA_ID_1425080,Human_miRNA_ID_2727717 Clinvar_Rec_695 RMVar_hsa_circ_108153,RMVar_hsa_circ_260717,RMVar_hsa_circ_83977,RMVar_hsa_circ_260745,RMVar_hsa_circ_17295,RMVar_hsa_circ_52706 107822 RMVar_ID_107822 Human_SNP_ID_417666034 m1A Human chr9 - 134842278 134842278 134842278 GCGGCTCCTAGCCCATGAAGCAAGCCGGCCCCACTTCAAATCCAAATTTCTGTGACGCTTCACCG GCGGCTCCTAGCCCATGAAGCAAGCCGGCCCCGCTTCAAATCCAAATTTCTGTGACGCTTCACCG T C LOC101448202,LOC101448202:2,LOC101448202:3,LOC101448202:4,LOC101448202:5 RNACentral:URS0000D577CE,RNACentral:URS000075CC5B,RNACentral:URS0000D5A355,RNACentral:URS0000D5A859,RNACentral:URS0000D599F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:134842230..134842621;chr9:134842233..134842388 26863196 MeRIP-seq:(Medium) rs532411382 Functional Loss SNV dbSNP153 33..33 33 - - - 107823 RMVar_ID_107823 Human_SNP_ID_417666097 m1A Human chr9 - 134842396 134842396 134842396 GAAGTCAGGTGGGAGGGGAGGGAGAAGCCTTCACTGTCCAGGGTCAGGACGTGCACGGGACACTC GAAGTCAGGTGGGAGGGGAGGGAGAAGCCTTCGCTGTCCAGGGTCAGGACGTGCACGGGACACTC T C LOC101448202,LOC101448202:2,LOC101448202:3,LOC101448202:4,LOC101448202:5 RNACentral:URS0000D577CE,RNACentral:URS000075CC5B,RNACentral:URS0000D5A355,RNACentral:URS0000D5A859,RNACentral:URS0000D599F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134842201..134842513 26863196 MeRIP-seq:(Medium) rs1427318934 Functional Loss SNV dbSNP153 33..33 33 - - - 107824 RMVar_ID_107824 Human_SNP_ID_417666205 m1A Human chr9 + 134842744 134842744 134842744 TTCCCCTGACCTTCAAAAAATGTTCCAAGGTAAGCCTCGTAAAGGTCATCCCACCATCACCAAAG TTCCCCTGACCTTCAAAAAATGTTCCAAGGTAGGCCTCGTAAAGGTCATCCCACCATCACCAAAG A G COL5A1 Ensembl:ENSG00000130635 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134842696..134842813 26863196 MeRIP-seq:(Medium) rs1365225572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24522760 Human_miRNA_ID_1398163 RMVar_hsa_circ_83977,RMVar_hsa_circ_260745 107825 RMVar_ID_107825 Human_SNP_ID_417666436 m1A Human chr9 + 134843529 134843529 134843529 CTCTAAGATCAATGCACGTCACTTTCCTTTCCACTGGGCAGGATAGCCAAGCACACTCCCTCCTG CTCTAAGATCAATGCACGTCACTTTCCTTTCCCCTGGGCAGGATAGCCAAGCACACTCCCTCCTG A C COL5A1 Ensembl:ENSG00000130635 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134843478..134843561 26863196 MeRIP-seq:(Medium) rs1430229673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8699600,Human_RBP_ID_16613093,Human_RBP_ID_17435884,Human_RBP_ID_27543861 Human_miRNA_ID_507513,Human_miRNA_ID_514713 RMVar_hsa_circ_83977,RMVar_hsa_circ_260745 107826 RMVar_ID_107826 Human_SNP_ID_417666682 m1A Human chr9 - 134844389 134844388 134844389 TGACAGGAGAAAAGGACAAATTGGATGGGATGAGAAATGAAAACAGAATCACATGACCTAGACGC TGACAGGAGAAAAGGACAAATTGGATGGGATG_GAAATGAAAACAGAATCACATGACCTAGACGC CT C LOC101448202,LOC101448202:2,LOC101448202:3,LOC101448202:4,LOC101448202:5 RNACentral:URS0000D577CE,RNACentral:URS000075CC5B,RNACentral:URS0000D5A355,RNACentral:URS0000D5A859,RNACentral:URS0000D599F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:134844201..134844525 26863196 MeRIP-seq:(Medium) rs1399634857 Functional Loss DEL dbSNP153 33..33 33 - - - 107827 RMVar_ID_107827 Human_SNP_ID_417666688 m1A Human chr9 + 134844401 134844401 134844401 TGTGATTCTGTTTTCATTTCTCATCCCATCCAATTTGTCCTTTTCTCCTGTCATTTTCTTCCTCT TGTGATTCTGTTTTCATTTCTCATCCCATCCAGTTTGTCCTTTTCTCCTGTCATTTTCTTCCTCT A G COL5A1 Ensembl:ENSG00000130635 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134844351..134844469 26863196 MeRIP-seq:(Medium) rs1047223250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21659145,Human_RBP_ID_24442547,Human_RBP_ID_24522790,Human_RBP_ID_27543868 RMVar_hsa_circ_83977,RMVar_hsa_circ_260745 107828 RMVar_ID_107828 Human_SNP_ID_417666689 m1A Human chr9 + 134844401 134844401 134844401 TGTGATTCTGTTTTCATTTCTCATCCCATCCAATTTGTCCTTTTCTCCTGTCATTTTCTTCCTCT TGTGATTCTGTTTTCATTTCTCATCCCATCCATTTTGTCCTTTTCTCCTGTCATTTTCTTCCTCT A T COL5A1 Ensembl:ENSG00000130635 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134844351..134844469 26863196 MeRIP-seq:(Medium) rs1047223250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21659145,Human_RBP_ID_24442547,Human_RBP_ID_24522790,Human_RBP_ID_27543868 RMVar_hsa_circ_83977,RMVar_hsa_circ_260745 107829 RMVar_ID_107829 Human_SNP_ID_417672869 m1A Human chr9 - 134864202 134864202 134864202 TGGAATCCAGCCCTTGAGGAAATCTCTTGCAGAGAATCTGCCGTGAGTCCACAGAAGTTTAGGAA TGGAATCCAGCCCTTGAGGAAATCTCTTGCAGGGAATCTGCCGTGAGTCCACAGAAGTTTAGGAA T C LOC101448202,LOC101448202:2,LOC101448202:3,LOC101448202:4,LOC101448202:5 RNACentral:URS0000D577CE,RNACentral:URS000075CC5B,RNACentral:URS0000D5A355,RNACentral:URS0000D5A859,RNACentral:URS0000D599F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134864197..134864288 26863196 MeRIP-seq:(Medium) rs902846265 Functional Loss SNV dbSNP153 33..33 33 - - - 107830 RMVar_ID_107830 Human_SNP_ID_676010246 m1A Human chr20 + 20020608 20020608 20020608 CCAAGAAACCCAGGTGGAGGGGCCAGGAAGGCATCTGGGCATGGGCGTCTCAAGATTAGGTCTGA CCAAGAAACCCAGGTGGAGGGGCCAGGAAGGCGTCTGGGCATGGGCGTCTCAAGATTAGGTCTGA A G NAA20 Ensembl:ENSG00000173418 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:20020604..20020887 26863196 MeRIP-seq:(Medium) rs1250903734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6982950,Human_RBP_ID_14045846 RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 107831 RMVar_ID_107831 Human_SNP_ID_676010596 m1A Human chr20 - 20021861 20021861 20021861 CCGATGCTGTGGGCAGCTCACCAGCACATCCCAGCACACCATTCCCAAATCTGCATTCTGAAAAC CCGATGCTGTGGGCAGCTCACCAGCACATCCCGGCACACCATTCCCAAATCTGCATTCTGAAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:20021857..20022051 26863196 MeRIP-seq:(Medium) rs74650410 Functional Loss SNV dbSNP153 33..33 33 - - - 107832 RMVar_ID_107832 Human_SNP_ID_676018261 m1A Human chr20 + 20052349 20052349 20052349 TTCCCGGCCGCGGTGGAGGCCGCCATGTCTGCAGCAGTCGACCTCTGGACACCTGTCCCCGGCAC TTCCCGGCCGCGGTGGAGGCCGCCATGTCTGCCGCAGTCGACCTCTGGACACCTGTCCCCGGCAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:20052299..20052389 26863196 MeRIP-seq:(Medium) rs772726100 Functional Loss SNV dbSNP153 33..33 33 - - - 107833 RMVar_ID_107833 Human_SNP_ID_676018262 m1A Human chr20 + 20052349 20052349 20052349 TTCCCGGCCGCGGTGGAGGCCGCCATGTCTGCAGCAGTCGACCTCTGGACACCTGTCCCCGGCAC TTCCCGGCCGCGGTGGAGGCCGCCATGTCTGCTGCAGTCGACCTCTGGACACCTGTCCCCGGCAC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:20052299..20052389 26863196 MeRIP-seq:(Medium) rs772726100 Functional Loss SNV dbSNP153 33..33 33 - - - 107834 RMVar_ID_107834 Human_SNP_ID_676152507 m1A Human chr20 - 20610620 20610620 20610620 AAAAGGGGAGCTAGCTGAAGTCGGTGGCATACATGGTGGGCGAGGTTTAAGGTGGGTGGTACTAA AAAAGGGGAGCTAGCTGAAGTCGGTGGCATACGTGGTGGGCGAGGTTTAAGGTGGGTGGTACTAA T C RALGAPA2 Ensembl:ENSG00000188559 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:20610536..20610678 26863196 MeRIP-seq:(Medium) rs570436820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108306,RMVar_hsa_circ_208971,RMVar_hsa_circ_51570,RMVar_hsa_circ_16489,RMVar_hsa_circ_10175,RMVar_hsa_circ_60157,RMVar_hsa_circ_9471,RMVar_hsa_circ_5958,RMVar_hsa_circ_329526,RMVar_hsa_circ_60968,RMVar_hsa_circ_75215,RMVar_hsa_circ_312927,RMVar_hsa_circ_208992,RMVar_hsa_circ_208991,RMVar_hsa_circ_66594,RMVar_hsa_circ_48998,RMVar_hsa_circ_61832,RMVar_hsa_circ_331749,RMVar_hsa_circ_97552,RMVar_hsa_circ_208996,RMVar_hsa_circ_107047,RMVar_hsa_circ_208998,RMVar_hsa_circ_208999,RMVar_hsa_circ_349367,RMVar_hsa_circ_341354,RMVar_hsa_circ_67668,RMVar_hsa_circ_209001,RMVar_hsa_circ_62619,RMVar_hsa_circ_209003,RMVar_hsa_circ_352689,RMVar_hsa_circ_374961,RMVar_hsa_circ_209004,RMVar_hsa_circ_326414,RMVar_hsa_circ_67371,RMVar_hsa_circ_50522,RMVar_hsa_circ_209006,RMVar_hsa_circ_59906,RMVar_hsa_circ_209005 107835 RMVar_ID_107835 Human_SNP_ID_676152563 m1A Human chr20 + 20610923 20610923 20610923 CTTTCTCAGCATCTCTCCCATCACCTGTGGACATTGTCCTCTCTAGGTAAGCCCATCCTGTGGCT CTTTCTCAGCATCTCTCCCATCACCTGTGGACCTTGTCCTCTCTAGGTAAGCCCATCCTGTGGCT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:20610878..20610961 26863196 MeRIP-seq:(Medium) rs1189487818 Functional Loss SNV dbSNP153 33..33 33 - - - 107836 RMVar_ID_107836 Human_SNP_ID_676321577 m1A Human chr20 - 21303370 21303370 21303370 CCATAGCGGCACACGGCTGGAGGCGGCGGCCGACCGGCTGACGAGCGTAACCAAAGAGACGGGAG CCATAGCGGCACACGGCTGGAGGCGGCGGCCGGCCGGCTGACGAGCGTAACCAAAGAGACGGGAG T C AL117332.1 Ensembl:ENSG00000275457 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:21303071..21303461 26863196 MeRIP-seq:(Medium) rs1373752314 Functional Loss SNV dbSNP153 33..33 33 - - - 107837 RMVar_ID_107837 Human_SNP_ID_676321612 m1A Human chr20 - 21303444 21303444 21303444 CACCTTCTCTTCCACGCAGTTGACTATGATGGACGGGTACTTGCGGCTGAGCCAGCGGAAGAACG CACCTTCTCTTCCACGCAGTTGACTATGATGGTCGGGTACTTGCGGCTGAGCCAGCGGAAGAACG T A AL117332.1 Ensembl:ENSG00000275457 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:21303326..21303475 26863196 MeRIP-seq:(Medium) rs888094572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4637909,Human_RBP_ID_5596410 107838 RMVar_ID_107838 Human_SNP_ID_676321613 m1A Human chr20 - 21303444 21303444 21303444 CACCTTCTCTTCCACGCAGTTGACTATGATGGACGGGTACTTGCGGCTGAGCCAGCGGAAGAACG CACCTTCTCTTCCACGCAGTTGACTATGATGGGCGGGTACTTGCGGCTGAGCCAGCGGAAGAACG T C AL117332.1 Ensembl:ENSG00000275457 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:21303326..21303475 26863196 MeRIP-seq:(Medium) rs888094572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4637909,Human_RBP_ID_5596410 107839 RMVar_ID_107839 Human_SNP_ID_676329228 m1A Human chr20 + 21335133 21335133 21335133 CTGAAGAGATGGGAAGCCATGCTCAAGGGGTCACAGTGAGATGGACAGGCACTTCGTCCGTGGAC CTGAAGAGATGGGAAGCCATGCTCAAGGGGTCCCAGTGAGATGGACAGGCACTTCGTCCGTGGAC A C XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:21335129..21335218 26863196 MeRIP-seq:(Medium) rs189353314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6984262,Human_RBP_ID_14048892,Human_RBP_ID_23284339 RMVar_hsa_circ_819,RMVar_hsa_circ_14874,RMVar_hsa_circ_93034,RMVar_hsa_circ_355257,RMVar_hsa_circ_360478,RMVar_hsa_circ_324073,RMVar_hsa_circ_340776,RMVar_hsa_circ_286364,RMVar_hsa_circ_291629,RMVar_hsa_circ_273020,RMVar_hsa_circ_30544,RMVar_hsa_circ_209027,RMVar_hsa_circ_209029,RMVar_hsa_circ_209031,RMVar_hsa_circ_209030,RMVar_hsa_circ_209028,RMVar_hsa_circ_91212,RMVar_hsa_circ_209026,RMVar_hsa_circ_37582,RMVar_hsa_circ_209035,RMVar_hsa_circ_50329,RMVar_hsa_circ_48448,RMVar_hsa_circ_301776,RMVar_hsa_circ_313546,RMVar_hsa_circ_15219,RMVar_hsa_circ_85823,RMVar_hsa_circ_209037,RMVar_hsa_circ_209038,RMVar_hsa_circ_85384,RMVar_hsa_circ_209040,RMVar_hsa_circ_209041,RMVar_hsa_circ_75446,RMVar_hsa_circ_83273,RMVar_hsa_circ_209042,RMVar_hsa_circ_112591,RMVar_hsa_circ_117092,RMVar_hsa_circ_209045,RMVar_hsa_circ_209046,RMVar_hsa_circ_119745,RMVar_hsa_circ_209047,RMVar_hsa_circ_209048,RMVar_hsa_circ_95093,RMVar_hsa_circ_114062,RMVar_hsa_circ_103785,RMVar_hsa_circ_209049,RMVar_hsa_circ_209050 107840 RMVar_ID_107840 Human_SNP_ID_676329229 m1A Human chr20 + 21335133 21335133 21335133 CTGAAGAGATGGGAAGCCATGCTCAAGGGGTCACAGTGAGATGGACAGGCACTTCGTCCGTGGAC CTGAAGAGATGGGAAGCCATGCTCAAGGGGTCGCAGTGAGATGGACAGGCACTTCGTCCGTGGAC A G XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:21335129..21335218 26863196 MeRIP-seq:(Medium) rs189353314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6984262,Human_RBP_ID_14048892,Human_RBP_ID_23284339 RMVar_hsa_circ_819,RMVar_hsa_circ_14874,RMVar_hsa_circ_93034,RMVar_hsa_circ_355257,RMVar_hsa_circ_360478,RMVar_hsa_circ_324073,RMVar_hsa_circ_340776,RMVar_hsa_circ_286364,RMVar_hsa_circ_291629,RMVar_hsa_circ_273020,RMVar_hsa_circ_30544,RMVar_hsa_circ_209027,RMVar_hsa_circ_209029,RMVar_hsa_circ_209031,RMVar_hsa_circ_209030,RMVar_hsa_circ_209028,RMVar_hsa_circ_91212,RMVar_hsa_circ_209026,RMVar_hsa_circ_37582,RMVar_hsa_circ_209035,RMVar_hsa_circ_50329,RMVar_hsa_circ_48448,RMVar_hsa_circ_301776,RMVar_hsa_circ_313546,RMVar_hsa_circ_15219,RMVar_hsa_circ_85823,RMVar_hsa_circ_209037,RMVar_hsa_circ_209038,RMVar_hsa_circ_85384,RMVar_hsa_circ_209040,RMVar_hsa_circ_209041,RMVar_hsa_circ_75446,RMVar_hsa_circ_83273,RMVar_hsa_circ_209042,RMVar_hsa_circ_112591,RMVar_hsa_circ_117092,RMVar_hsa_circ_209045,RMVar_hsa_circ_209046,RMVar_hsa_circ_119745,RMVar_hsa_circ_209047,RMVar_hsa_circ_209048,RMVar_hsa_circ_95093,RMVar_hsa_circ_114062,RMVar_hsa_circ_103785,RMVar_hsa_circ_209049,RMVar_hsa_circ_209050 107841 RMVar_ID_107841 Human_SNP_ID_676329589 m1A Human chr20 + 21336778 21336778 21336778 AAGTGCCACAAAGAAAACTAAAGCAGGTGAGGAGGCATCTGGGAAGGGAGAGGTTGGGCATTACA AAGTGCCACAAAGAAAACTAAAGCAGGTGAGGCGGCATCTGGGAAGGGAGAGGTTGGGCATTACA A C XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:21336773..21336848 26863196 MeRIP-seq:(Medium) rs950537258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6984276,Human_RBP_ID_14048946 RMVar_hsa_circ_819,RMVar_hsa_circ_14874,RMVar_hsa_circ_93034,RMVar_hsa_circ_355257,RMVar_hsa_circ_360478,RMVar_hsa_circ_324073,RMVar_hsa_circ_340776,RMVar_hsa_circ_286364,RMVar_hsa_circ_291629,RMVar_hsa_circ_273020,RMVar_hsa_circ_30544,RMVar_hsa_circ_209027,RMVar_hsa_circ_209029,RMVar_hsa_circ_209031,RMVar_hsa_circ_209030,RMVar_hsa_circ_209028,RMVar_hsa_circ_91212,RMVar_hsa_circ_209026,RMVar_hsa_circ_37582,RMVar_hsa_circ_209035,RMVar_hsa_circ_50329,RMVar_hsa_circ_48448,RMVar_hsa_circ_301776,RMVar_hsa_circ_313546,RMVar_hsa_circ_15219,RMVar_hsa_circ_85823,RMVar_hsa_circ_209037,RMVar_hsa_circ_209038,RMVar_hsa_circ_85384,RMVar_hsa_circ_209040,RMVar_hsa_circ_209041,RMVar_hsa_circ_75446,RMVar_hsa_circ_83273,RMVar_hsa_circ_209042,RMVar_hsa_circ_112591,RMVar_hsa_circ_117092,RMVar_hsa_circ_209045,RMVar_hsa_circ_209046,RMVar_hsa_circ_119745,RMVar_hsa_circ_209047,RMVar_hsa_circ_209048,RMVar_hsa_circ_95093,RMVar_hsa_circ_114062,RMVar_hsa_circ_103785,RMVar_hsa_circ_209049,RMVar_hsa_circ_209050 107842 RMVar_ID_107842 Human_SNP_ID_676337461 m1A Human chr20 - 21368455 21368454 21368455 TCCTGAGCCTCTTGGCATCACATGGCTATAAAAGGACCCAACACAAGAAAAAAAAATTGTATAGT TCCTGAGCCTCTTGGCATCACATGGCTATAAA_GGACCCAACACAAGAAAAAAAAATTGTATAGT CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:21368451..21368500 32194978 MeRIP-seq:(Medium) rs1438519084 Functional Loss DEL dbSNP153 33..33 33 - - - 107843 RMVar_ID_107843 Human_SNP_ID_676341799 m1A Human chr20 + 21386905 21386905 21386905 TTGGGGCTGAACCTCTGCTCCCATGGAACCGGATGCTGCAAACCCAGAATGCAGCCTTCCAGCCA TTGGGGCTGAACCTCTGCTCCCATGGAACCGGTTGCTGCAAACCCAGAATGCAGCCTTCCAGCCA A T XRN2 Ensembl:ENSG00000088930 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:21386876..21386925 32194978 MeRIP-seq:(Medium) rs371099785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14050166,Human_RBP_ID_22672439,Human_RBP_ID_23005119 Human_Splice_Rec_2066006 Human_miRNA_ID_1938544,Human_miRNA_ID_1949644,Human_miRNA_ID_3002856 RMVar_hsa_circ_30235,RMVar_hsa_circ_76580,RMVar_hsa_circ_209060 107844 RMVar_ID_107844 Human_SNP_ID_676865821 m1A Human chr20 - 23350858 23350858 23350858 TGGAGGCTTACTCTGGGTCACCGGGGCCCCAGAGCCGGGGGACTTTCCGGCGCAGTTCCGCGGCT TGGAGGCTTACTCTGGGTCACCGGGGCCCCAGTGCCGGGGGACTTTCCGGCGCAGTTCCGCGGCT T A NXT1-AS1 Ensembl:ENSG00000234832 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:23350807..23350927 26863196 MeRIP-seq:(Medium) rs1274940999 Functional Loss SNV dbSNP153 33..33 33 - - - 107845 RMVar_ID_107845 Human_SNP_ID_676869028 m1A Human chr20 - 23362239 23362239 23362239 GGGCCGGAGCCAGGCCTACGGGCCGCGCACTCACCTCCCAGCCGGCGCCCCCGCTGCAGCCGCTG GGGCCGGAGCCAGGCCTACGGGCCGCGCACTCCCCTCCCAGCCGGCGCCCCCGCTGCAGCCGCTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:23362220..23362295 26863196 MeRIP-seq:(Medium) rs1038841095 Functional Loss SNV dbSNP153 33..33 33 - - - 107846 RMVar_ID_107846 Human_SNP_ID_676869864 m1A Human chr20 - 23365241 23365241 23365241 GGCCCTGCTTTCTTTGACAATTCCTCCAACTCAGCACCTGCCTGGCAACCCTCATTTTTGGAAAC GGCCCTGCTTTCTTTGACAATTCCTCCAACTCGGCACCTGCCTGGCAACCCTCATTTTTGGAAAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:23365054..23365387 26863196 MeRIP-seq:(Medium) rs1160824828 Functional Loss SNV dbSNP153 33..33 33 - - - 107847 RMVar_ID_107847 Human_SNP_ID_676871110 m1A Human chr20 - 23369685 23369685 23369685 CTTGTCGGTGAATGTCCGTCCGCACGCATTGCACATGAATGGCCTCTCCCCTGTGTGGATGCGGC CTTGTCGGTGAATGTCCGTCCGCACGCATTGCCCATGAATGGCCTCTCCCCTGTGTGGATGCGGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:23369597..23369733 26863196 MeRIP-seq:(Medium) rs1344010932 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23896967 107848 RMVar_ID_107848 Human_SNP_ID_676940768 m1A Human chr20 + 23633724 23633724 23633724 GTATGCACCGCACACCGGGGCTATGAGAAGCAAGAAGGAAGGAGGGAGGGCAGAGCCCCTTGCTG GTATGCACCGCACACCGGGGCTATGAGAAGCAGGAAGGAAGGAGGGAGGGCAGAGCCCCTTGCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:23633676..23633750 26863196 MeRIP-seq:(Medium) rs555982384 Functional Loss SNV dbSNP153 33..33 33 - - - 107849 RMVar_ID_107849 Human_SNP_ID_676942021 m1A Human chr20 - 23637723 23637720 23637723 GGGAGGCCCCATGGACGCCAGCGTGGAGGAGGAGGGTGTGCGGCGTGCACTGGACTTTGCCGTCG GGGAGGCCCCATGGACGCCAGCGTGGAGGAGG___GTGTGCGGCGTGCACTGGACTTTGCCGTCG CCCT C CST3 Ensembl:ENSG00000101439 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:23637701..23637725 26863196 MeRIP-seq:(Medium) rs1239120039 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_244319,Human_RBP_ID_560292,Human_RBP_ID_778792,Human_RBP_ID_831459,Human_RBP_ID_927301,Human_RBP_ID_4638379,Human_RBP_ID_5119143,Human_RBP_ID_5323176,Human_RBP_ID_8260237,Human_RBP_ID_8529439,Human_RBP_ID_17658996,Human_RBP_ID_17968545,Human_RBP_ID_18444054,Human_RBP_ID_22452945,Human_RBP_ID_22767207 Human_miRNA_ID_2079479,Human_miRNA_ID_2081795 RMVar_hsa_circ_209078,RMVar_hsa_circ_91022,RMVar_hsa_circ_209079,RMVar_hsa_circ_96177 107850 RMVar_ID_107850 Human_SNP_ID_676942056 m1A Human chr20 - 23637758 23637758 23637758 GCCGGCTCCAGTCCCGGCAAGCCGCCGCGCCTAGTGGGAGGCCCCATGGACGCCAGCGTGGAGGA GCCGGCTCCAGTCCCGGCAAGCCGCCGCGCCTGGTGGGAGGCCCCATGGACGCCAGCGTGGAGGA T C CST3 Ensembl:ENSG00000101439 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs6138024 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_831459,Human_RBP_ID_927301,Human_RBP_ID_4638381,Human_RBP_ID_17659254,Human_RBP_ID_22452945,Human_RBP_ID_26488961 Human_miRNA_ID_2868883 RMVar_hsa_circ_209078,RMVar_hsa_circ_91022,RMVar_hsa_circ_209079,RMVar_hsa_circ_96177 107851 RMVar_ID_107851 Human_SNP_ID_676942116 m1A Human chr20 + 23637837 23637837 23637837 CCAGGGCCACGGCCAGGATGGCCAGCAGGAGCAGCGGGGCGCGCAGGGGCCCGGCCATGGTCGGC CCAGGGCCACGGCCAGGATGGCCAGCAGGAGCTGCGGGGCGCGCAGGGGCCCGGCCATGGTCGGC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:23637738..23637988 26863196 MeRIP-seq:(Medium) rs777804660 Functional Loss SNV dbSNP153 33..33 33 - - - 107852 RMVar_ID_107852 Human_SNP_ID_677309708 m1A Human chr20 + 24963973 24963973 24963973 TCCGGAAGGCACCGCTGTCGCTGAGTTCTAGGACGAGGCTGTACCGCGGCACAAACTTCATCACC TCCGGAAGGCACCGCTGTCGCTGAGTTCTAGGGCGAGGCTGTACCGCGGCACAAACTTCATCACC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:24963401..24964025 32194978 MeRIP-seq:(Medium) rs1294127611 Functional Loss SNV dbSNP153 33..33 33 - - - 107853 RMVar_ID_107853 Human_SNP_ID_677310015 m1A Human chr20 + 24965031 24965027 24965031 TCTCTTCCCCCTAAGAGATCTCATCCTCTCTCACTATTACAACTAGTCACTTTCCCAGAAAGCTC TCTCTTCCCCCTAAGAGATCTCATCCTCT____CTATTACAACTAGTCACTTTCCCAGAAAGCTC TCTCA T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:24965010..24965094 26863196 MeRIP-seq:(Medium) rs1334883352 Functional Loss DEL dbSNP153 30..33 33 - - - 107854 RMVar_ID_107854 Human_SNP_ID_677368671 m1A Human chr20 - 25195768 25195768 25195768 GTCTTTTGGGCTCCCCCGCCCCGGCCGGCGCCACCCCGGCCTCCACCCGCGGGATACGACCCCAC GTCTTTTGGGCTCCCCCGCCCCGGCCGGCGCCGCCCCGGCCTCCACCCGCGGGATACGACCCCAC T C LOC101926889,LOC101926889:2 RNACentral:URS000075F0A3,RNACentral:URS00008B636A lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:25195726..25195862;chr20:25195726..25195918;chr20:25195701..25195933 26863196 MeRIP-seq:(Medium) rs1167834351 Functional Loss SNV dbSNP153 33..33 33 - - - 107855 RMVar_ID_107855 Human_SNP_ID_677375306 m1A Human chr20 + 25222207 25222207 25222207 AACGAGGAGGAGGTGGTGTGGCTTGGTGGGGGACACCAGGAGGAAATGAGATCGAAGGGTTGGAG AACGAGGAGGAGGTGGTGTGGCTTGGTGGGGGGCACCAGGAGGAAATGAGATCGAAGGGTTGGAG A G ENTPD6 Ensembl:ENSG00000197586 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:25222166..25222332;chr20:25221945..25222375 26863196 MeRIP-seq:(Medium) rs914885856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960081,Human_RBP_ID_8203749,Human_RBP_ID_18950346,Human_RBP_ID_21982812,Human_RBP_ID_22361436,Human_RBP_ID_22479078,Human_RBP_ID_22743623,Human_RBP_ID_26788196 107856 RMVar_ID_107856 Human_SNP_ID_677381991 m1A Human chr20 - 25248151 25248151 25248151 GCCATCGCGCCGGCGGAGGCGGAGGAAAAGAGATGGAGGAGGAAAGCGGCGGCACACGCGAACGC GCCATCGCGCCGGCGGAGGCGGAGGAAAAGAGGTGGAGGAGGAAAGCGGCGGCACACGCGAACGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25248101..25248199 26863196 MeRIP-seq:(Medium) rs199837145 Functional Loss SNV dbSNP153 33..33 33 - - - 107857 RMVar_ID_107857 Human_SNP_ID_677390163 m1A Human chr20 + 25276063 25276063 25276063 GCCCTTGGTGGTAGCGGAGCTGATGTCTCTGGATGCAGGGGAACCTGGGGGCTTGTCAAGGAGAG GCCCTTGGTGGTAGCGGAGCTGATGTCTCTGGGTGCAGGGGAACCTGGGGGCTTGTCAAGGAGAG A G PYGB Ensembl:ENSG00000100994 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25276057..25276131 26863196 MeRIP-seq:(Medium) rs1053257368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84952,RMVar_hsa_circ_209110,RMVar_hsa_circ_120697,RMVar_hsa_circ_22082,RMVar_hsa_circ_114902,RMVar_hsa_circ_334489,RMVar_hsa_circ_209111,RMVar_hsa_circ_96483,RMVar_hsa_circ_209113,RMVar_hsa_circ_36354,RMVar_hsa_circ_83855,RMVar_hsa_circ_98054,RMVar_hsa_circ_209114,RMVar_hsa_circ_209115,RMVar_hsa_circ_108357,RMVar_hsa_circ_26111,RMVar_hsa_circ_209116,RMVar_hsa_circ_209117 107858 RMVar_ID_107858 Human_SNP_ID_677390247 m1A Human chr20 + 25276379 25276379 25276379 GGATGATTCTTCAGTCAAAGCCATTCCTGAGGAAGGTCAAGTGAGAAGATAGGTCTGGTCTGGGG GGATGATTCTTCAGTCAAAGCCATTCCTGAGGTAGGTCAAGTGAGAAGATAGGTCTGGTCTGGGG A T PYGB Ensembl:ENSG00000100994 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25276376..25276627 26863196 MeRIP-seq:(Medium) rs375409599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9431210 RMVar_hsa_circ_84952,RMVar_hsa_circ_209110,RMVar_hsa_circ_120697,RMVar_hsa_circ_22082,RMVar_hsa_circ_114902,RMVar_hsa_circ_334489,RMVar_hsa_circ_209111,RMVar_hsa_circ_96483,RMVar_hsa_circ_209113,RMVar_hsa_circ_36354,RMVar_hsa_circ_83855,RMVar_hsa_circ_98054,RMVar_hsa_circ_209114,RMVar_hsa_circ_209115,RMVar_hsa_circ_108357,RMVar_hsa_circ_26111,RMVar_hsa_circ_209116,RMVar_hsa_circ_209117 107859 RMVar_ID_107859 Human_SNP_ID_677391624 m1A Human chr20 + 25280321 25280321 25280321 CTGTGCATACACCAACCACACTGTGCTGCCTGAGGCCTTGGAGCGCTGGCCCGTGTCCATGTTTG CTGTGCATACACCAACCACACTGTGCTGCCTGGGGCCTTGGAGCGCTGGCCCGTGTCCATGTTTG A G PYGB Ensembl:ENSG00000100994 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:25280251..25280325 32194978 MeRIP-seq:(Medium) rs141342768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19005231,Human_RBP_ID_27820102 Human_Splice_Rec_2067714,Human_Splice_Rec_2067715 Human_miRNA_ID_2663755,Human_miRNA_ID_2682208 RMVar_hsa_circ_84952,RMVar_hsa_circ_209110,RMVar_hsa_circ_120697,RMVar_hsa_circ_114902,RMVar_hsa_circ_209111,RMVar_hsa_circ_96483,RMVar_hsa_circ_209113,RMVar_hsa_circ_83855,RMVar_hsa_circ_98054,RMVar_hsa_circ_209114,RMVar_hsa_circ_209115,RMVar_hsa_circ_108357,RMVar_hsa_circ_26111,RMVar_hsa_circ_93386,RMVar_hsa_circ_42303,RMVar_hsa_circ_209116,RMVar_hsa_circ_209117,RMVar_hsa_circ_80338,RMVar_hsa_circ_102382,RMVar_hsa_circ_209118,RMVar_hsa_circ_83369,RMVar_hsa_circ_209119,RMVar_hsa_circ_209120,RMVar_hsa_circ_209121,RMVar_hsa_circ_50897,RMVar_hsa_circ_209123,RMVar_hsa_circ_114080,RMVar_hsa_circ_306622,RMVar_hsa_circ_209122 107860 RMVar_ID_107860 Human_SNP_ID_677397531 m1A Human chr20 + 25297836 25297836 25297836 CCAGAGCACTACAGCCTTTTATTGAGTGGGGCAAGTGCTGGGCTGTGGTCGTGCCCTGACAGCAT CCAGAGCACTACAGCCTTTTATTGAGTGGGGCGAGTGCTGGGCTGTGGTCGTGCCCTGACAGCAT A G PYGB Ensembl:ENSG00000100994 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:25297794..25297925 32194978 MeRIP-seq:(Medium) rs201921762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560474,Human_RBP_ID_1594006 Human_miRNA_ID_2056749 RMVar_hsa_circ_84952,RMVar_hsa_circ_209110,RMVar_hsa_circ_120697,RMVar_hsa_circ_209111,RMVar_hsa_circ_96483,RMVar_hsa_circ_209113,RMVar_hsa_circ_83855,RMVar_hsa_circ_209115,RMVar_hsa_circ_108357,RMVar_hsa_circ_93386,RMVar_hsa_circ_209117,RMVar_hsa_circ_80338,RMVar_hsa_circ_209118,RMVar_hsa_circ_83369,RMVar_hsa_circ_209120,RMVar_hsa_circ_110827,RMVar_hsa_circ_209121,RMVar_hsa_circ_209123,RMVar_hsa_circ_114080,RMVar_hsa_circ_114594,RMVar_hsa_circ_209124,RMVar_hsa_circ_103364,RMVar_hsa_circ_209125,RMVar_hsa_circ_209126,RMVar_hsa_circ_90258,RMVar_hsa_circ_80572,RMVar_hsa_circ_113080,RMVar_hsa_circ_209129,RMVar_hsa_circ_209130,RMVar_hsa_circ_91811,RMVar_hsa_circ_209131,RMVar_hsa_circ_209132 107861 RMVar_ID_107861 Human_SNP_ID_677422768 m1A Human chr20 + 25390604 25390604 25390604 GCCCGTCAGGCGTAGGTTCTGCTTCAGGCGGCAGTCGGCGTCCAGCGCCGCGGCGGCCGAGCCGG GCCCGTCAGGCGTAGGTTCTGCTTCAGGCGGCCGTCGGCGTCCAGCGCCGCGGCGGCCGAGCCGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:25390521..25390792 26863196 MeRIP-seq:(Medium) rs1391542746 Functional Loss SNV dbSNP153 33..33 33 - - - 107862 RMVar_ID_107862 Human_SNP_ID_677422831 m1A Human chr20 - 25390691 25390691 25390691 CTGGCCCTGTCGGCCGCGGGATGAGGAAGCGGACCGAGCCCGTCGCCTTGGAGCATGAGCGCTGC CTGGCCCTGTCGGCCGCGGGATGAGGAAGCGGGCCGAGCCCGTCGCCTTGGAGCATGAGCGCTGC T C ABHD12 Ensembl:ENSG00000100997 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:25390582..25390800 26863196 MeRIP-seq:(Medium) rs759098488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560502,Human_RBP_ID_830940,Human_RBP_ID_4659299,Human_RBP_ID_6986063,Human_RBP_ID_19005245 107863 RMVar_ID_107863 Human_SNP_ID_677422893 m1A Human chr20 - 25390756 25390756 25390756 GGCTCTGGGTGGCGGCGGCTGTGAGCGGCGGCACTGCGGCGCAGGCCAGCGGGCGCCGTCGGCGG GGCTCTGGGTGGCGGCGGCTGTGAGCGGCGGCGCTGCGGCGCAGGCCAGCGGGCGCCGTCGGCGG T C ABHD12 Ensembl:ENSG00000100997 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:25390480..25390834 26863410 MeRIP-seq:(Medium) rs1375961017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830940,Human_RBP_ID_4638907,Human_RBP_ID_18423020,Human_RBP_ID_18463280,Human_RBP_ID_22452968 107864 RMVar_ID_107864 Human_SNP_ID_677422894 m1A Human chr20 - 25390756 25390756 25390756 GGCTCTGGGTGGCGGCGGCTGTGAGCGGCGGCACTGCGGCGCAGGCCAGCGGGCGCCGTCGGCGG GGCTCTGGGTGGCGGCGGCTGTGAGCGGCGGCCCTGCGGCGCAGGCCAGCGGGCGCCGTCGGCGG T G ABHD12 Ensembl:ENSG00000100997 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:25390480..25390834 26863410 MeRIP-seq:(Medium) rs1375961017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_830940,Human_RBP_ID_4638907,Human_RBP_ID_18423020,Human_RBP_ID_18463280,Human_RBP_ID_22452968 107865 RMVar_ID_107865 Human_SNP_ID_677427622 m1A Human chr20 - 25407849 25407849 25407849 GTTGCCCTTCGGGCGCGCGATGCAGCTCGCGGATCAGTTCCATGGCTTTTTCGCAGAACATGGCG GTTGCCCTTCGGGCGCGCGATGCAGCTCGCGGCTCAGTTCCATGGCTTTTTCGCAGAACATGGCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:25407826..25407850 32194978 MeRIP-seq:(Medium) rs752803071 Functional Loss SNV dbSNP153 33..33 33 - - - 107866 RMVar_ID_107866 Human_SNP_ID_677437958 m1A Human chr20 + 25447712 25447712 25447712 GGCCAGGCTGTGTTGAACTCCTGAGCTAAAGCAATACACTTGCCTCGTCCTCCCCATGTGCTGGG GGCCAGGCTGTGTTGAACTCCTGAGCTAAAGCGATACACTTGCCTCGTCCTCCCCATGTGCTGGG A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs893714161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6986390,Human_RBP_ID_17510859,Human_RBP_ID_17968801,Human_RBP_ID_18321127,Human_RBP_ID_26489046,Human_RBP_ID_27700476 Human_miRNA_ID_269188,Human_miRNA_ID_2050014 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 107867 RMVar_ID_107867 Human_SNP_ID_677440735 m1A Human chr20 + 25458096 25458096 25458096 GGCCTCTGGTCCCTGTTCCCCTGGAACATGCCAAATACCCCCTACCCCAGGGCCTCTGCTGCTCC GGCCTCTGGTCCCTGTTCCCCTGGAACATGCCGAATACCCCCTACCCCAGGGCCTCTGCTGCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:25457975..25458493;chr20:25457979..25458469 26863196 MeRIP-seq:(Medium) rs1352255851 Functional Loss SNV dbSNP153 33..33 33 - - - 107868 RMVar_ID_107868 Human_SNP_ID_677440801 m1A Human chr20 - 25458368 25458368 25458368 CGCCTGGATGCACAGCGGGTAAGTGGGGATGCAGCGAGAGATGGCTGACGAGATGAGGAGGAGGG CGCCTGGATGCACAGCGGGTAAGTGGGGATGCGGCGAGAGATGGCTGACGAGATGAGGAGGAGGG T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:25458233..25458409 26863196 MeRIP-seq:(Medium) rs1159679759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116613,RMVar_hsa_circ_340059,RMVar_hsa_circ_209162 107869 RMVar_ID_107869 Human_SNP_ID_677441514 m1A Human chr20 - 25460978 25460976 25460978 CGAGCAGGGGCCTCAGGGAGGGGAGCCGGCTCAGGGGATGCTTGTGGAGGGGGTGGCTCAAGGGA CGAGCAGGGGCCTCAGGGAGGGGAGCCGGCTC__GGGATGCTTGTGGAGGGGGTGGCTCAAGGGA CCT C NINL Ensembl:ENSG00000101004 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25460973..25461079 26863196 MeRIP-seq:(Medium) rs1283022640 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_13,RMVar_hsa_circ_116613,RMVar_hsa_circ_340059,RMVar_hsa_circ_209162,RMVar_hsa_circ_337728 107870 RMVar_ID_107870 Human_SNP_ID_677443647 m1A Human chr20 + 25468652 25468648 25468652 CACTGGTGGGCGCCCCCCTGCCCTGTCCCCCAATTCTCACTGGTGGGTGCCCCTCTGCCCTGTCC CACTGGTGGGCGCCCCCCTGCCCTGTCCC____TTCTCACTGGTGGGTGCCCCTCTGCCCTGTCC CCCAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25468648..25469504 26863196 MeRIP-seq:(Medium) rs1241893690 Functional Loss DEL dbSNP153 30..33 33 - - - 107871 RMVar_ID_107871 Human_SNP_ID_677443651 m1A Human chr20 + 25468652 25468652 25468652 CACTGGTGGGCGCCCCCCTGCCCTGTCCCCCAATTCTCACTGGTGGGTGCCCCTCTGCCCTGTCC CACTGGTGGGCGCCCCCCTGCCCTGTCCCCCAGTTCTCACTGGTGGGTGCCCCTCTGCCCTGTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25468648..25469504 26863196 MeRIP-seq:(Medium) rs1392779312 Functional Loss SNV dbSNP153 33..33 33 - - - 107872 RMVar_ID_107872 Human_SNP_ID_677443739 m1A Human chr20 - 25468825 25468825 25468825 GCGGTGGGGCGCCCACCAGTGAGAGTTGGGACAGGGTAGGGGGGTGCCCACCAGTGAGAGTCAGG GCGGTGGGGCGCCCACCAGTGAGAGTTGGGACGGGGTAGGGGGGTGCCCACCAGTGAGAGTCAGG T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25468822..25469015 26863196 MeRIP-seq:(Medium) rs532682324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13,RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_34148,RMVar_hsa_circ_72750,RMVar_hsa_circ_340664,RMVar_hsa_circ_209163,RMVar_hsa_circ_73820,RMVar_hsa_circ_270593,RMVar_hsa_circ_296399,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209164,RMVar_hsa_circ_209165,RMVar_hsa_circ_209166 107873 RMVar_ID_107873 Human_SNP_ID_677443968 m1A Human chr20 - 25469298 25469298 25469298 GGTACTCACCAGTGAGAGTCGGGGGACAGGGCAGTGGGGCGCCCACCAGTGAGAGTTGGGACAGG GGTACTCACCAGTGAGAGTCGGGGGACAGGGCGGTGGGGCGCCCACCAGTGAGAGTTGGGACAGG T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25469291..25469404 26863196 MeRIP-seq:(Medium) rs1470047562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13,RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_34148,RMVar_hsa_circ_72750,RMVar_hsa_circ_340664,RMVar_hsa_circ_209163,RMVar_hsa_circ_73820,RMVar_hsa_circ_270593,RMVar_hsa_circ_296399,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209164,RMVar_hsa_circ_209165,RMVar_hsa_circ_209166 107874 RMVar_ID_107874 Human_SNP_ID_677446021 m1A Human chr20 - 25476415 25476414 25476415 AGACGCCTCGCAAACCCAGCCACGGATGTGGGAGCCACCCCTGAGGCCGGCCGCTTCGTGCAGGG AGACGCCTCGCAAACCCAGCCACGGATGTGGG_GCCACCCCTGAGGCCGGCCGCTTCGTGCAGGG CT C NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25476170..25479205 26863196 MeRIP-seq:(Medium) rs869282953 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22081272 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_73820,RMVar_hsa_circ_296399,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209165,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_326296 107875 RMVar_ID_107875 Human_SNP_ID_677446023 m1A Human chr20 - 25476415 25476415 25476415 AGACGCCTCGCAAACCCAGCCACGGATGTGGGAGCCACCCCTGAGGCCGGCCGCTTCGTGCAGGG AGACGCCTCGCAAACCCAGCCACGGATGTGGGTGCCACCCCTGAGGCCGGCCGCTTCGTGCAGGG T A NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25476170..25479205 26863196 MeRIP-seq:(Medium) rs200097181 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22081272 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_73820,RMVar_hsa_circ_296399,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209165,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_326296 107876 RMVar_ID_107876 Human_SNP_ID_677446371 m1A Human chr20 + 25476955 25476955 25476955 AGGGCTGCAGCTTCAGTGCCCTCTCCAGCTCCAGCTGCTCCGACCTCTGGCTCCCGCGTGGCAGG AGGGCTGCAGCTTCAGTGCCCTCTCCAGCTCCGGCTGCTCCGACCTCTGGCTCCCGCGTGGCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:25476736..25477074 26863196 MeRIP-seq:(Medium) rs1378513732 Functional Loss SNV dbSNP153 33..33 33 - - - 107877 RMVar_ID_107877 Human_SNP_ID_677446372 m1A Human chr20 + 25476955 25476955 25476955 AGGGCTGCAGCTTCAGTGCCCTCTCCAGCTCCAGCTGCTCCGACCTCTGGCTCCCGCGTGGCAGG AGGGCTGCAGCTTCAGTGCCCTCTCCAGCTCCTGCTGCTCCGACCTCTGGCTCCCGCGTGGCAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:25476736..25477074 26863196 MeRIP-seq:(Medium) rs1378513732 Functional Loss SNV dbSNP153 33..33 33 - - - 107878 RMVar_ID_107878 Human_SNP_ID_677447123 m1A Human chr20 + 25479142 25479142 25479142 GCACGCTGACCTCGCGCCTGCGAGCCTGCTCCATGTCCTTCCTCTCCTTCTCAAAGTTCCTTTTC GCACGCTGACCTCGCGCCTGCGAGCCTGCTCCGTGTCCTTCCTCTCCTTCTCAAAGTTCCTTTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:25476693..25479205 26863196 MeRIP-seq:(Medium) rs201802713 Functional Loss SNV dbSNP153 33..33 33 - - - 107879 RMVar_ID_107879 Human_SNP_ID_677449919 m1A Human chr20 - 25489987 25489987 25489987 GGAGCCTGATGAGCCACTGGCCTGTGTCTCCTAGGAAAACAGTCGCCTACAGAAGGAGATTGTGG GGAGCCTGATGAGCCACTGGCCTGTGTCTCCTGGGAAAACAGTCGCCTACAGAAGGAGATTGTGG T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25489950..25490029 26863196 MeRIP-seq:(Medium) rs770472903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18444084,Human_RBP_ID_22671324 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_61669,RMVar_hsa_circ_8424,RMVar_hsa_circ_353317,RMVar_hsa_circ_79648,RMVar_hsa_circ_209167,RMVar_hsa_circ_56253 107880 RMVar_ID_107880 Human_SNP_ID_677450410 m1A Human chr20 - 25491437 25491437 25491437 CGGAGCGAGAGCTGTTCTGGGAGCAGGCCCACAGGCAGAGGGCCGCGCTGGAGTGGGACGTGGGG CGGAGCGAGAGCTGTTCTGGGAGCAGGCCCACGGGCAGAGGGCCGCGCTGGAGTGGGACGTGGGG T C NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25491388..25491559 26863196 MeRIP-seq:(Medium) rs1277842758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925428,Human_RBP_ID_9390242,Human_RBP_ID_19005260,Human_RBP_ID_23005132 Human_Splice_Rec_2068142,Human_Splice_Rec_2068143,Human_Splice_Rec_2068186,Human_Splice_Rec_2068187,Human_Splice_Rec_2068225 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_61669,RMVar_hsa_circ_8424,RMVar_hsa_circ_353317,RMVar_hsa_circ_79648,RMVar_hsa_circ_209167,RMVar_hsa_circ_56253,RMVar_hsa_circ_366513 107881 RMVar_ID_107881 Human_SNP_ID_677459317 m1A Human chr20 - 25526524 25526524 25526524 AGCTCAGGGAAGTCTACAGCAGCTGCGACACCACGGGGACTGGCTTTCTGGACCGCCAGGAGCTG AGCTCAGGGAAGTCTACAGCAGCTGCGACACCTCGGGGACTGGCTTTCTGGACCGCCAGGAGCTG T A NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25526473..25526649 26863196 MeRIP-seq:(Medium) rs773118633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925435,Human_RBP_ID_4661675,Human_RBP_ID_9388868,Human_RBP_ID_19005269 Human_Splice_Rec_2068124,Human_Splice_Rec_2068168 RMVar_hsa_circ_37100,RMVar_hsa_circ_61669,RMVar_hsa_circ_209169,RMVar_hsa_circ_273541,RMVar_hsa_circ_289764,RMVar_hsa_circ_339508 107882 RMVar_ID_107882 Human_SNP_ID_677459318 m1A Human chr20 - 25526524 25526524 25526524 AGCTCAGGGAAGTCTACAGCAGCTGCGACACCACGGGGACTGGCTTTCTGGACCGCCAGGAGCTG AGCTCAGGGAAGTCTACAGCAGCTGCGACACCGCGGGGACTGGCTTTCTGGACCGCCAGGAGCTG T C NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25526473..25526649 26863196 MeRIP-seq:(Medium) rs773118633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925435,Human_RBP_ID_4661675,Human_RBP_ID_9388868,Human_RBP_ID_19005269 Human_Splice_Rec_2068124,Human_Splice_Rec_2068168 RMVar_hsa_circ_37100,RMVar_hsa_circ_61669,RMVar_hsa_circ_209169,RMVar_hsa_circ_273541,RMVar_hsa_circ_289764,RMVar_hsa_circ_339508 107883 RMVar_ID_107883 Human_SNP_ID_677459343 m1A Human chr20 - 25526587 25526587 25526587 TCTTCCCTTGCACACTGCCAGCCTGCTATGGGATGGATGAAGAAGAGAACCACTATGTCTCGCAG TCTTCCCTTGCACACTGCCAGCCTGCTATGGGTTGGATGAAGAAGAGAACCACTATGTCTCGCAG T A NINL Ensembl:ENSG00000101004 Protein coding start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:25526562..25526651 26863410 MeRIP-seq:(Medium) rs774359722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19106113,Human_RBP_ID_25626886 Human_Splice_Rec_2068124,Human_Splice_Rec_2068168 RMVar_hsa_circ_37100,RMVar_hsa_circ_61669,RMVar_hsa_circ_209169,RMVar_hsa_circ_273541,RMVar_hsa_circ_289764,RMVar_hsa_circ_339508 107884 RMVar_ID_107884 Human_SNP_ID_677474628 m1A Human chr20 + 25585502 25585502 25585502 GCCGTCCGCCCGCGCGGGGCCAGGAGCGCGGCACCACCCCCGTACCGCCGGCCGCTCTTTGTGTC GCCGTCCGCCCGCGCGGGGCCAGGAGCGCGGCCCCACCCCCGTACCGCCGGCCGCTCTTTGTGTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:25585422..25585508 26863196 MeRIP-seq:(Medium) rs895048185 Functional Loss SNV dbSNP153 33..33 33 - - - 107885 RMVar_ID_107885 Human_SNP_ID_677474631 m1A Human chr20 + 25585505 25585505 25585505 GTCCGCCCGCGCGGGGCCAGGAGCGCGGCACCACCCCCGTACCGCCGGCCGCTCTTTGTGTCTGG GTCCGCCCGCGCGGGGCCAGGAGCGCGGCACCGCCCCCGTACCGCCGGCCGCTCTTTGTGTCTGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:25585437..25585509 26863196 MeRIP-seq:(Medium) rs994162033 Functional Loss SNV dbSNP153 33..33 33 - - - 107886 RMVar_ID_107886 Human_SNP_ID_677478476 m1A Human chr20 + 25601700 25601700 25601700 TGCACACAGCCATCTCACACACACCTCTCCACACACCTACATACACACACACAACCATCTCACAC TGCACACAGCCATCTCACACACACCTCTCCACGCACCTACATACACACACACAACCATCTCACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25601614..25602055 26863196 MeRIP-seq:(Medium) rs1160916802 Functional Loss SNV dbSNP153 33..33 33 - - - 107887 RMVar_ID_107887 Human_SNP_ID_677483852 m1A Human chr20 - 25623961 25623961 25623961 CAGGCGGCGGTGGCAAGGCTACGGTTCGCGCCAGCGGCCGGCGCTATGGGGCTGAGCCGCGTGCG CAGGCGGCGGTGGCAAGGCTACGGTTCGCGCCTGCGGCCGGCGCTATGGGGCTGAGCCGCGTGCG T A NANP Ensembl:ENSG00000170191 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25623861..25623963 26863196 MeRIP-seq:(Medium) rs534649559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4639101,Human_RBP_ID_18423029 107888 RMVar_ID_107888 Human_SNP_ID_677483853 m1A Human chr20 - 25623961 25623961 25623961 CAGGCGGCGGTGGCAAGGCTACGGTTCGCGCCAGCGGCCGGCGCTATGGGGCTGAGCCGCGTGCG CAGGCGGCGGTGGCAAGGCTACGGTTCGCGCCGGCGGCCGGCGCTATGGGGCTGAGCCGCGTGCG T C NANP Ensembl:ENSG00000170191 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25623861..25623963 26863196 MeRIP-seq:(Medium) rs534649559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4639101,Human_RBP_ID_18423029 107889 RMVar_ID_107889 Human_SNP_ID_677483912 m1A Human chr20 + 25624081 25624081 25624081 GACCATCTCCCGGCGCGGGTGGAATTCCCGCGATCTGTCTCATTCCCTGCGCCGCCGAGAAAAGT GACCATCTCCCGGCGCGGGTGGAATTCCCGCGGTCTGTCTCATTCCCTGCGCCGCCGAGAAAAGT A G ZNF337-AS1 Ensembl:ENSG00000213742 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:25624030..25624115 26863196 MeRIP-seq:(Medium) rs1156645084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660855 Human_Splice_Rec_2068233,Human_Splice_Rec_2068239,Human_Splice_Rec_2068247 RMVar_hsa_circ_89148,RMVar_hsa_circ_209172 107890 RMVar_ID_107890 Human_SNP_ID_677495790 m1A Human chr20 + 25674999 25674999 25674999 AAAGCTTGTAACAAAGCAAAGTTACTCTCCTGAGTGTGTCCTCTGATGGATGGTGAGATATAACT AAAGCTTGTAACAAAGCAAAGTTACTCTCCTGTGTGTGTCCTCTGATGGATGGTGAGATATAACT A T ZNF337-AS1 Ensembl:ENSG00000213742 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:25674948..25675297 32194978 MeRIP-seq:(Medium) rs1201967676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3657055 Human_Splice_Rec_2068245,Human_Splice_Rec_2068263 Human_miRNA_ID_1959766,Human_miRNA_ID_3063452,Human_miRNA_ID_3147632,Human_miRNA_ID_3212992 RMVar_hsa_circ_119360,RMVar_hsa_circ_209176,RMVar_hsa_circ_209177,RMVar_hsa_circ_47939 107891 RMVar_ID_107891 Human_SNP_ID_677496615 m1A Human chr20 - 25676832 25676831 25676833 AGCTCAAGGAGGAGGAACAGTGTAGTGGAAATAGAGTCTAGTCAAGGCCAGAGGGAAAATCCTAC AGCTCAAGGAGGAGGAACAGTGTAGTGGAAA__GAGTCTAGTCAAGGCCAGAGGGAAAATCCTAC CTA C ZNF337 Ensembl:ENSG00000130684 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25676737..25676870 26863196 MeRIP-seq:(Medium) rs1569007388 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14055447 RMVar_hsa_circ_209180,RMVar_hsa_circ_111563 107892 RMVar_ID_107892 Human_SNP_ID_677501616 m1A Human chr20 + 25696730 25696729 25696731 GCCCTTCTTCCTGCGCCGGAAGGGCGCGCTGCAGAGAGGGACCCGCAGGAGCGCAGCTCACCGGG GCCCTTCTTCCTGCGCCGGAAGGGCGCGCTGC__AGAGGGACCCGCAGGAGCGCAGCTCACCGGG CAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:25696679..25696793 26863196 MeRIP-seq:(Medium) rs996007063 Functional Loss DEL dbSNP153 33..34 33 - - - 107893 RMVar_ID_107893 Human_SNP_ID_677501617 m1A Human chr20 + 25696730 25696730 25696730 GCCCTTCTTCCTGCGCCGGAAGGGCGCGCTGCAGAGAGGGACCCGCAGGAGCGCAGCTCACCGGG GCCCTTCTTCCTGCGCCGGAAGGGCGCGCTGCGGAGAGGGACCCGCAGGAGCGCAGCTCACCGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:25696679..25696793 26863196 MeRIP-seq:(Medium) rs976439402 Functional Loss SNV dbSNP153 33..33 33 - - - 107894 RMVar_ID_107894 Human_SNP_ID_677534446 m1A Human chr20 - 25863135 25863135 25863135 ATGCCAGGACTCGCAAAGGGCCGACCAGAATGAGGAAATCCCAGGCGGAGTCCGGGGGAGGCAGC ATGCCAGGACTCGCAAAGGGCCGACCAGAATGTGGAAATCCCAGGCGGAGTCCGGGGGAGGCAGC T A FAM182B Ensembl:ENSG00000175170 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25863099..25863263 26863196 MeRIP-seq:(Medium) rs1322466484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2068363,Human_Splice_Rec_2068367 107895 RMVar_ID_107895 Human_SNP_ID_677577026 m1A Human chr20 - 26009885 26009885 26009885 ACAAAAGGACCGGAGCCGGATTCCTCACCCTCAGCTTTCTCCAGTTCCGCTCGGGGCCAGCCTGG ACAAAAGGACCGGAGCCGGATTCCTCACCCTCGGCTTTCTCCAGTTCCGCTCGGGGCCAGCCTGG T C AL078587.1 Ensembl:ENSG00000231081 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:26009851..26009918;chr20:26009854..26009965 26863196 MeRIP-seq:(Medium) rs1333173911 Functional Loss SNV dbSNP153 33..33 33 - - - 107896 RMVar_ID_107896 Human_SNP_ID_677617479 m1A Human chr20 + 26209262 26209262 26209262 GCCCACCGCGATCGCTCACAGGGCCCGTGCGCACCCGCCAGAGGGGAGCACCGGACGTGCGCTCG GCCCACCGCGATCGCTCACAGGGCCCGTGCGCCCCCGCCAGAGGGGAGCACCGGACGTGCGCTCG A C lnc-GINS1-13,lnc-GINS1-13:2,lnc-GINS1-13:3,lnc-GINS1-13:4,lnc-GINS1-13:5 RNACentral:URS00008C0C9F,RNACentral:URS0000D5E240,RNACentral:URS0000D57C49,RNACentral:URS0000D56CDD,RNACentral:URS0000D599EC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:26209232..26209301 26863196 MeRIP-seq:(Medium) rs1033607038 Functional Loss SNV dbSNP153 33..33 33 - - - 107897 RMVar_ID_107897 Human_SNP_ID_677617480 m1A Human chr20 + 26209262 26209262 26209262 GCCCACCGCGATCGCTCACAGGGCCCGTGCGCACCCGCCAGAGGGGAGCACCGGACGTGCGCTCG GCCCACCGCGATCGCTCACAGGGCCCGTGCGCGCCCGCCAGAGGGGAGCACCGGACGTGCGCTCG A G lnc-GINS1-13,lnc-GINS1-13:2,lnc-GINS1-13:3,lnc-GINS1-13:4,lnc-GINS1-13:5 RNACentral:URS00008C0C9F,RNACentral:URS0000D5E240,RNACentral:URS0000D57C49,RNACentral:URS0000D56CDD,RNACentral:URS0000D599EC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:26209232..26209301 26863196 MeRIP-seq:(Medium) rs1033607038 Functional Loss SNV dbSNP153 33..33 33 - - - 107898 RMVar_ID_107898 Human_SNP_ID_677904233 m1A Human chr20 - 28582584 28582582 28582584 GCCAGTCAAAGGCTGTTCTCTGGCTAGGACACAGGGGACTCCAGCCAGCATGCCCTAATAGAAGT GCCAGTCAAAGGCTGTTCTCTGGCTAGGACAC__GGGACTCCAGCCAGCATGCCCTAATAGAAGT CCT C FRG1CP Ensembl:ENSG00000282826 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:28582520..28582625 32194978 MeRIP-seq:(Medium) rs1339013030 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_309497 107899 RMVar_ID_107899 Human_SNP_ID_677904234 m1A Human chr20 - 28582584 28582583 28582584 GCCAGTCAAAGGCTGTTCTCTGGCTAGGACACAGGGGACTCCAGCCAGCATGCCCTAATAGAAGT GCCAGTCAAAGGCTGTTCTCTGGCTAGGACAC_GGGGACTCCAGCCAGCATGCCCTAATAGAAGT CT C FRG1CP Ensembl:ENSG00000282826 Pseudogene intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:28582520..28582625 32194978 MeRIP-seq:(Medium) rs1278142378 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_309497 107900 RMVar_ID_107900 Human_SNP_ID_677910170 m1A Human chr20 - 28600452 28600452 28600452 TCTATATAAATTATGTCCTGTAGTAAGAAGAAAAAGAACAAAGATAAGAAAAGAAAAAGAGAAGA TCTATATAAATTATGTCCTGTAGTAAGAAGAATAAGAACAAAGATAAGAAAAGAAAAAGAGAAGA T A FRG1CP Ensembl:ENSG00000282826 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:28600404..28600508 26863196 MeRIP-seq:(Medium) rs1242588510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9347883 Human_Splice_Rec_2069710,Human_Splice_Rec_2069711,Human_Splice_Rec_2069722,Human_Splice_Rec_2069723,Human_Splice_Rec_2069732,Human_Splice_Rec_2069733,Human_Splice_Rec_2069750,Human_Splice_Rec_2069751 107901 RMVar_ID_107901 Human_SNP_ID_677987934 m1A Human chr20 + 28889805 28889795 28889805 CCATTCCATTCCATTCCATTCTGTTACATTCCATTCCACTCCATTCCAGTCCACTCTACTCCATT CCATTCCATTCCATTCCATTCTG__________TTCCACTCCATTCCAGTCCACTCTACTCCATT GTTACATTCCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:28889755..28889839 26863196 MeRIP-seq:(Medium) rs1323623225 Functional Loss DEL dbSNP153 24..33 33 - - - 107902 RMVar_ID_107902 Human_SNP_ID_678103929 m1A Human chr20 - 29298525 29298525 29298525 TGATCGGGGATTGCAATTATTCCCCATGAACGAGGAATTCCCAGTAAGTGTGGGTCATAGGCTTG TGATCGGGGATTGCAATTATTCCCCATGAACGTGGAATTCCCAGTAAGTGTGGGTCATAGGCTTG T A RF01960-008,RF01960-008:2,RF01960-008:3,RF01960-008:4,RF01960-008:5,RF01960-008:6,RF01960-008:7,RF01960-008:8 RNACentral:URS00008D094F,RNACentral:URS000062FB25,RNACentral:URS00008C6B7A,RNACentral:URS00008D14ED,RNACentral:URS00008C9FD4,RNACentral:URS00008D0497,RNACentral:URS00008CAEAC,RNACentral:URS00008CA83A rRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA exon,intron,intron,intron,exon,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:29298501..29298575 26863196 MeRIP-seq:(Medium) rs1395792922 Functional Loss SNV dbSNP153 33..33 33 - - - 107903 RMVar_ID_107903 Human_SNP_ID_678104876 m1A Human chr20 - 29299976 29299976 29299976 ACTGTGGTAATTCTAGAGCTAATACATGCCAAAGGGCGCTGACCCCCTTCGCGGGGAAGATGCGT ACTGTGGTAATTCTAGAGCTAATACATGCCAAGGGGCGCTGACCCCCTTCGCGGGGAAGATGCGT T C RF01960-008,RF01960-008:2,RF01960-008:3,RF01960-008:4,RF01960-008:5,RF01960-008:6,RF01960-008:7 RNACentral:URS00008D094F,RNACentral:URS000062FB25,RNACentral:URS00008C6B7A,RNACentral:URS00008D14ED,RNACentral:URS00008C9FD4,RNACentral:URS00008CAEAC,RNACentral:URS00008CA83A rRNA,rRNA,rRNA,rRNA,rRNA,rRNA,rRNA exon,intron,intron,intron,exon,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:29299951..29299975 26863196 MeRIP-seq:(Medium) rs1360607032 Functional Loss SNV dbSNP153 33..33 33 - - - 107904 RMVar_ID_107904 Human_SNP_ID_678104886 m1A Human chr20 + 29299986 29299986 29299986 CCCGCGAAGGGGGTCAGCGCCCTTTGGCATGTATTAGCTCTAGAATTACCACAGTTTTCCAAGTA CCCGCGAAGGGGGTCAGCGCCCTTTGGCATGTGTTAGCTCTAGAATTACCACAGTTTTCCAAGTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:29299913..29300064 26863196 MeRIP-seq:(Medium) rs1215302329 Functional Loss SNV dbSNP153 33..33 33 - - - 107905 RMVar_ID_107905 Human_SNP_ID_678484587 m1A Human chr20 + 30377247 30377247 30377247 TTTGGGTGAAGACGGAGGCGGGTTCTGGACAGACGTAGGCTGTCAGGGAGTGTTTACTTCGCCTC TTTGGGTGAAGACGGAGGCGGGTTCTGGACAGCCGTAGGCTGTCAGGGAGTGTTTACTTCGCCTC A C lnc-DEFB115-5,lnc-ANKRD20A2-22,lnc-DEFB115-5:2,lnc-DEFB115-5:3 RNACentral:URS00008C1224,RNACentral:URS00009C53CC,RNACentral:URS00008C33AD,RNACentral:URS00009B255F lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:30377224..30377400 26863196 MeRIP-seq:(Medium) rs796485842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5445475 107906 RMVar_ID_107906 Human_SNP_ID_678527026 m1A Human chr20 + 30514026 30514026 30514026 CGGAACGGCACTCACCTATCTCTCAGGACCAAATGAACCATGTTCAACTGCTGTTCACCTGAGAC CGGAACGGCACTCACCTATCTCTCAGGACCAACTGAACCATGTTCAACTGCTGTTCACCTGAGAC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:30513976..30514025 26863196 MeRIP-seq:(Medium) rs1209714707 Functional Loss SNV dbSNP153 33..33 33 - - - 107907 RMVar_ID_107907 Human_SNP_ID_678527046 m1A Human chr20 - 30514073 30514073 30514073 AAGGCCGAAGTGGAGAAGGGTTCCATGTGAACAGCAGTTGAACATGGGTCTCAGGTGAACAGCAG AAGGCCGAAGTGGAGAAGGGTTCCATGTGAACGGCAGTTGAACATGGGTCTCAGGTGAACAGCAG T C RF02543-034 RNACentral:URS00008C8EB4 rRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:30514051..30514125 26863196 MeRIP-seq:(Medium) rs1199500870 Functional Loss SNV dbSNP153 33..33 33 - - - 107908 RMVar_ID_107908 Human_SNP_ID_678668472 m1A Human chr20 - 31053442 31053442 31053442 CCATGCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCACCCCATT CCATGCCATTCCATTCCATTCCATTCCATTCCGTTCCATTCCATTCCATTCCATTCCACCCCATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31053398..31053484 26863196 MeRIP-seq:(Medium) rs1301320537 Functional Loss SNV dbSNP153 33..33 33 - - - 107909 RMVar_ID_107909 Human_SNP_ID_678668893 m1A Human chr20 + 31054297 31054297 31054297 AATGGAATGGAATGGAATCAACTAGAATGGAAAGGAATGGAATGGAATGGAATGCAGTGGAATGG AATGGAATGGAATGGAATCAACTAGAATGGAATGGAATGGAATGGAATGGAATGCAGTGGAATGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31054230..31054359 26863196 MeRIP-seq:(Medium) rs1316067367 Functional Loss SNV dbSNP153 33..33 33 - - - 107910 RMVar_ID_107910 Human_SNP_ID_678669209 m1A Human chr20 + 31054890 31054890 31054890 GAATGAAATGGAATGGAATGGAATGGAATGGAATCAACCCGAGTGGAATGTAATGGAATGGAATG GAATGAAATGGAATGGAATGGAATGGAATGGAGTCAACCCGAGTGGAATGTAATGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31054847..31055298 26863196 MeRIP-seq:(Medium) rs1017226387 Functional Loss SNV dbSNP153 33..33 33 - - - 107911 RMVar_ID_107911 Human_SNP_ID_678670163 m1A Human chr20 - 31056666 31056662 31056667 CCATTCCATTCCATTCCATTCCATTCCATTCCATTCAATTACACTTGCATTGATTCCATTCCATT CCATTCCATTCCATTCCATTCCATTCCATTC_____AATTACACTTGCATTGATTCCATTCCATT TGAATG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31056635..31056733 26863196 MeRIP-seq:(Medium) rs1167984761 Functional Loss DEL dbSNP153 32..36 33 - - - 107912 RMVar_ID_107912 Human_SNP_ID_678671727 m1A Human chr20 - 31061645 31061645 31061645 TTACATCCTATTCCGTTCCGTTCCATTCCTTTACATTGGATTGGATTCCATTCCATTCCATTCCA TTACATCCTATTCCGTTCCGTTCCATTCCTTTTCATTGGATTGGATTCCATTCCATTCCATTCCA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31061578..31061742 26863196 MeRIP-seq:(Medium) rs1305931529 Functional Loss SNV dbSNP153 33..33 33 - - - 107913 RMVar_ID_107913 Human_SNP_ID_678671882 m1A Human chr20 + 31062282 31062282 31062282 GAATGGAAAGGAATGGAATGGAATGGAATGGAATGGAATCAACCAGAGTGGAATGGAATGGAATG GAATGGAAAGGAATGGAATGGAATGGAATGGAGTGGAATCAACCAGAGTGGAATGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31062273..31062398 26863196 MeRIP-seq:(Medium) rs1199586434 Functional Loss SNV dbSNP153 33..33 33 - - - 107914 RMVar_ID_107914 Human_SNP_ID_678672061 m1A Human chr20 + 31062981 31062977 31062982 GGAATGAAAGGGAATGGAATCACCCCGAGTGGAATGGAATGGAATGGAATGGAATGCAATGGAAT GGAATGAAAGGGAATGGAATCACCCCGAG_____TGGAATGGAATGGAATGGAATGCAATGGAAT GTGGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31062932..31063017 26863196 MeRIP-seq:(Medium) rs1207420667 Functional Loss DEL dbSNP153 30..34 33 - - - 107915 RMVar_ID_107915 Human_SNP_ID_678672256 m1A Human chr20 - 31063769 31063769 31063769 TCGATTCCATTCGGGTTGACTCCATTGCTTTCAATTCCATTCCATTCCATTCCATTCTATTCCAT TCGATTCCATTCGGGTTGACTCCATTGCTTTCCATTCCATTCCATTCCATTCCATTCTATTCCAT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31063719..31063838 26863196 MeRIP-seq:(Medium) rs1303739219 Functional Loss SNV dbSNP153 33..33 33 - - - 107916 RMVar_ID_107916 Human_SNP_ID_678672560 m1A Human chr20 + 31064961 31064961 31064961 GGAATTGAATGTAATGGAATGGCATTGAATGGAATCAACACGAGTGGAATGGAATGGAATGGAAT GGAATTGAATGTAATGGAATGGCATTGAATGGCATCAACACGAGTGGAATGGAATGGAATGGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31064946..31065044 26863196 MeRIP-seq:(Medium) rs1456653549 Functional Loss SNV dbSNP153 33..33 33 - - - 107917 RMVar_ID_107917 Human_SNP_ID_678672736 m1A Human chr20 - 31065628 31065628 31065628 TCATTCCATACCATTCCATTCCACTCGGGTTCATTCTACTCCATTCCATTCCATTCCTGTACATT TCATTCCATACCATTCCATTCCACTCGGGTTCCTTCTACTCCATTCCATTCCATTCCTGTACATT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31065613..31065723 26863196 MeRIP-seq:(Medium) rs1316437563 Functional Loss SNV dbSNP153 33..33 33 - - - 107918 RMVar_ID_107918 Human_SNP_ID_678676262 m1A Human chr20 + 31074377 31074377 31074377 AACCCGAGTAGAATGCAATGGAAGGGAATGGAATCGAATGTAATGGAATGGCATTGAATGGAATC AACCCGAGTAGAATGCAATGGAAGGGAATGGATTCGAATGTAATGGAATGGCATTGAATGGAATC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31074151..31074449 26863196 MeRIP-seq:(Medium) rs984528648 Functional Loss SNV dbSNP153 33..33 33 - - - 107919 RMVar_ID_107919 Human_SNP_ID_678686913 m1A Human chr20 - 31103053 31103053 31103053 CCTTTCAATTCGTGTCCATTCCATTCCTTTCGAGTCCATTCCATTCCATTCTATTCCATGCGAGT CCTTTCAATTCGTGTCCATTCCATTCCTTTCGGGTCCATTCCATTCCATTCTATTCCATGCGAGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31103048..31103158 26863196 MeRIP-seq:(Medium) rs1483800410 Functional Loss SNV dbSNP153 33..33 33 - - - 107920 RMVar_ID_107920 Human_SNP_ID_678688459 m1A Human chr20 - 31157211 31157211 31157211 CCATTCCATTATATTCCATTCCATTCCACTCGATTTGATTCCATTCCATCCATTCCATTCCATTC CCATTCCATTATATTCCATTCCATTCCACTCGGTTTGATTCCATTCCATCCATTCCATTCCATTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31157206..31157375 26863196 MeRIP-seq:(Medium) rs1345405382 Functional Loss SNV dbSNP153 33..33 33 - - - 107921 RMVar_ID_107921 Human_SNP_ID_678688638 m1A Human chr20 - 31157490 31157480 31157490 CCATTCCATTCCATTCCATTCCATTGCATTCCACTACATTACGTTACATCACATTCCACTCGGGT CCATTCCATTCCATTCCATTCCATTGCATTCC__________GTTACATCACATTCCACTCGGGT CGTAATGTAGT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31157485..31157591 26863196 MeRIP-seq:(Medium) rs1374018211 Functional Loss DEL dbSNP153 33..42 33 - - - 107922 RMVar_ID_107922 Human_SNP_ID_678688649 m1A Human chr20 - 31157490 31157490 31157490 CCATTCCATTCCATTCCATTCCATTGCATTCCACTACATTACGTTACATCACATTCCACTCGGGT CCATTCCATTCCATTCCATTCCATTGCATTCCCCTACATTACGTTACATCACATTCCACTCGGGT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31157485..31157591 26863196 MeRIP-seq:(Medium) rs1251679510 Functional Loss SNV dbSNP153 33..33 33 - - - 107923 RMVar_ID_107923 Human_SNP_ID_678690127 m1A Human chr20 - 31162116 31162116 31162116 CCGTTCCACTCCATTCCACTCGAGTTGACTCCATTCCACTCCATTTCATTCGAGTCCATTCCGTT CCGTTCCACTCCATTCCACTCGAGTTGACTCCTTTCCACTCCATTTCATTCGAGTCCATTCCGTT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31162111..31162195 26863196 MeRIP-seq:(Medium) rs1384662346 Functional Loss SNV dbSNP153 33..33 33 - - - 107924 RMVar_ID_107924 Human_SNP_ID_678692224 m1A Human chr20 + 31165778 31165774 31165779 GACACGAATGCCATGGAAAGGATTGGACCCGAATGGAATGGAATGGAATGGAATGGAATGGAATG GACACGAATGCCATGGAAAGGATTGGACC_____GGAATGGAATGGAATGGAATGGAATGGAATG CCGAAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31165763..31165847 26863196 MeRIP-seq:(Medium) rs1162478797 Functional Loss DEL dbSNP153 30..34 33 - - - 107925 RMVar_ID_107925 Human_SNP_ID_678692241 m1A Human chr20 + 31165778 31165778 31165778 GACACGAATGCCATGGAAAGGATTGGACCCGAATGGAATGGAATGGAATGGAATGGAATGGAATG GACACGAATGCCATGGAAAGGATTGGACCCGAGTGGAATGGAATGGAATGGAATGGAATGGAATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31165763..31165847 26863196 MeRIP-seq:(Medium) rs1387246877 Functional Loss SNV dbSNP153 33..33 33 - - - 107926 RMVar_ID_107926 Human_SNP_ID_678701907 m1A Human chr20 + 31183827 31183827 31183827 AATGGAAAGGAATTGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAATGGCATGGAATGG AATGGAAAGGAATTGAATGGAATGGAATGGAAGGGAATGGAATGGAATGGAATGGCATGGAATGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31183814..31183975 26863196 MeRIP-seq:(Medium) rs930315807 Functional Loss SNV dbSNP153 33..33 33 - - - 107927 RMVar_ID_107927 Human_SNP_ID_678701908 m1A Human chr20 + 31183827 31183827 31183827 AATGGAAAGGAATTGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAATGGCATGGAATGG AATGGAAAGGAATTGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGCATGGAATGG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31183814..31183975 26863196 MeRIP-seq:(Medium) rs930315807 Functional Loss SNV dbSNP153 33..33 33 - - - 107928 RMVar_ID_107928 Human_SNP_ID_678703188 m1A Human chr20 + 31186308 31186302 31186308 TGGAATGGAATGAATGGAATCAACCTGACTGAAATGCAATGGAATGGAATGGAATGGAATGGAAT TGGAATGGAATGAATGGAATCAACCTG______ATGCAATGGAATGGAATGGAATGGAATGGAAT GACTGAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31186303..31186387 26863196 MeRIP-seq:(Medium) rs1568668915 Functional Loss DEL dbSNP153 28..33 33 - - - 107929 RMVar_ID_107929 Human_SNP_ID_678706784 m1A Human chr20 + 31192859 31192859 31192859 AATGGTATAGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAAAGGAATGGAATGA AATGGTATAGAATGGAATGGAATGGAATGGAACGGAATGGAATGGAATGGAAAGGAATGGAATGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31192836..31192933 26863196 MeRIP-seq:(Medium) rs988496284 Functional Loss SNV dbSNP153 33..33 33 - - - 107930 RMVar_ID_107930 Human_SNP_ID_678706785 m1A Human chr20 + 31192859 31192859 31192859 AATGGTATAGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGAAAGGAATGGAATGA AATGGTATAGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAAAGGAATGGAATGA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31192836..31192933 26863196 MeRIP-seq:(Medium) rs988496284 Functional Loss SNV dbSNP153 33..33 33 - - - 107931 RMVar_ID_107931 Human_SNP_ID_678710732 m1A Human chr20 + 31204733 31204733 31204733 GAAACGGAATGGAATGGAATGGACTCAAATGGAATGGAATGGAATGGAATGGAACGGAATAGAAT GAAACGGAATGGAATGGAATGGACTCAAATGGTATGGAATGGAATGGAATGGAACGGAATAGAAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31204688..31204774 26863196 MeRIP-seq:(Medium) rs1343718367 Functional Loss SNV dbSNP153 33..33 33 - - - 107932 RMVar_ID_107932 Human_SNP_ID_678722243 m1A Human chr20 + 31230659 31230659 31230659 ATGGAATGAAATGGAATGGAATGGAATGGAATAGAAAGGAATGGAATGGAATGGGATTGAATGGA ATGGAATGAAATGGAATGGAATGGAATGGAATCGAAAGGAATGGAATGGAATGGGATTGAATGGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31230609..31230693 26863196 MeRIP-seq:(Medium) rs878855993 Functional Loss SNV dbSNP153 33..33 33 - - - 107933 RMVar_ID_107933 Human_SNP_ID_678722244 m1A Human chr20 + 31230659 31230659 31230659 ATGGAATGAAATGGAATGGAATGGAATGGAATAGAAAGGAATGGAATGGAATGGGATTGAATGGA ATGGAATGAAATGGAATGGAATGGAATGGAATGGAAAGGAATGGAATGGAATGGGATTGAATGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31230609..31230693 26863196 MeRIP-seq:(Medium) rs878855993 Functional Loss SNV dbSNP153 33..33 33 - - - 107934 RMVar_ID_107934 Human_SNP_ID_678725079 m1A Human chr20 - 31235211 31235211 31235211 CCATTCCATTCCTTTCAATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCATTCCATTCCTTTCAATTCCATTCCTTTCCTTTCCATTCCATTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31235160..31235255 26863196 MeRIP-seq:(Medium) rs199967117 Functional Loss SNV dbSNP153 33..33 33 - - - 107935 RMVar_ID_107935 Human_SNP_ID_678725080 m1A Human chr20 - 31235211 31235211 31235211 CCATTCCATTCCTTTCAATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCATTCCATTCCTTTCAATTCCATTCCTTTCCGTTCCATTCCATTCCATTCCATTCCATTCCATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31235160..31235255 26863196 MeRIP-seq:(Medium) rs199967117 Functional Loss SNV dbSNP153 33..33 33 - - - 107936 RMVar_ID_107936 Human_SNP_ID_678725081 m1A Human chr20 - 31235211 31235211 31235211 CCATTCCATTCCTTTCAATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCATTCCATTCCTTTCAATTCCATTCCTTTCCCTTCCATTCCATTCCATTCCATTCCATTCCATT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31235160..31235255 26863196 MeRIP-seq:(Medium) rs199967117 Functional Loss SNV dbSNP153 33..33 33 - - - 107937 RMVar_ID_107937 Human_SNP_ID_678809019 m1A Human chr20 - 31514508 31514507 31514508 GTTCGGGATCCGACTCCAGCTCCGGTTGCTGCAGCAGGGACGCAGGCGGAGACACCGGCTCTGCA GTTCGGGATCCGACTCCAGCTCCGGTTGCTGC_GCAGGGACGCAGGCGGAGACACCGGCTCTGCA CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31514451..31514771 26863196 MeRIP-seq:(Medium) rs775810667 Functional Loss DEL dbSNP153 33..33 33 - - - 107938 RMVar_ID_107938 Human_SNP_ID_678809021 m1A Human chr20 - 31514508 31514508 31514508 GTTCGGGATCCGACTCCAGCTCCGGTTGCTGCAGCAGGGACGCAGGCGGAGACACCGGCTCTGCA GTTCGGGATCCGACTCCAGCTCCGGTTGCTGCGGCAGGGACGCAGGCGGAGACACCGGCTCTGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31514451..31514771 26863196 MeRIP-seq:(Medium) rs1004340665 Functional Loss SNV dbSNP153 33..33 33 - - - 107939 RMVar_ID_107939 Human_SNP_ID_678812171 m1A Human chr20 + 31527538 31527538 31527538 CAATCACCAGCCGGGATGCCGCCCGCTTCCCCATCATCGCCAGCTGCACACTCTTGGGGCTCTAC CAATCACCAGCCGGGATGCCGCCCGCTTCCCCGTCATCGCCAGCTGCACACTCTTGGGGCTCTAC A G HM13 Ensembl:ENSG00000101294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31527444..31527611 26863196 MeRIP-seq:(Medium) rs769600146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8529918,Human_RBP_ID_17510913,Human_RBP_ID_18193605,Human_RBP_ID_18770209,Human_RBP_ID_20639207,Human_RBP_ID_22452974,Human_RBP_ID_27483976 Human_Splice_Rec_2069968,Human_Splice_Rec_2069969,Human_Splice_Rec_2069992,Human_Splice_Rec_2069993,Human_Splice_Rec_2070016,Human_Splice_Rec_2070017,Human_Splice_Rec_2070038,Human_Splice_Rec_2070039,Human_Splice_Rec_2070064,Human_Splice_Rec_2070065,Human_Splice_Rec_2070088,Human_Splice_Rec_2070089,Human_Splice_Rec_2070112,Human_Splice_Rec_2070113,Human_Splice_Rec_2070116,Human_Splice_Rec_2070117,Human_Splice_Rec_2070138,Human_Splice_Rec_2070139,Human_Splice_Rec_2070148,Human_Splice_Rec_2070149,Human_Splice_Rec_2070164,Human_Splice_Rec_2070165,Human_Splice_Rec_2070188,Human_Splice_Rec_2070189 Human_miRNA_ID_2014116,Human_miRNA_ID_2014117,Human_miRNA_ID_2760516,Human_miRNA_ID_2760517,Human_miRNA_ID_2910814,Human_miRNA_ID_2910815 RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_348888,RMVar_hsa_circ_350215,RMVar_hsa_circ_369872,RMVar_hsa_circ_283515,RMVar_hsa_circ_209187,RMVar_hsa_circ_209188,RMVar_hsa_circ_209189 107940 RMVar_ID_107940 Human_SNP_ID_678814570 m1A Human chr20 - 31538216 31538216 31538216 ACAGGGCCAGGATTCCCAGCACGAAGAAATACATGGACAGCAGGAGGTTGATGTACTCCTGGGAG ACAGGGCCAGGATTCCCAGCACGAAGAAATACGTGGACAGCAGGAGGTTGATGTACTCCTGGGAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:31538201..31538250 26863196 MeRIP-seq:(Medium) rs372222178 Functional Loss SNV dbSNP153 33..33 33 - - - 107941 RMVar_ID_107941 Human_SNP_ID_678822449 m1A Human chr20 + 31569208 31569204 31569208 CAGAGGCATCAGCATCGAAGGGGCTGGAGAAGAAAGAGAAATGATGCAGCTGGTGCCCGAGCCTC CAGAGGCATCAGCATCGAAGGGGCTGGAG____AAGAGAAATGATGCAGCTGGTGCCCGAGCCTC GAAGA G HM13 Ensembl:ENSG00000101294 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31569110..31569464 26863196 MeRIP-seq:(Medium) rs1568804022 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_1197800,Human_RBP_ID_1594441,Human_RBP_ID_1927456,Human_RBP_ID_5119308,Human_RBP_ID_8529981,Human_RBP_ID_14059102,Human_RBP_ID_17659004,Human_RBP_ID_18193606,Human_RBP_ID_18770285,Human_RBP_ID_22452983,Human_RBP_ID_22767240,Human_RBP_ID_23133582 Human_Splice_Rec_2069990,Human_Splice_Rec_2070014,Human_Splice_Rec_2070036,Human_Splice_Rec_2070062,Human_Splice_Rec_2070086,Human_Splice_Rec_2070110,Human_Splice_Rec_2070136,Human_Splice_Rec_2070186,Human_Splice_Rec_2070228,Human_Splice_Rec_2070242,Human_Splice_Rec_2070276,Human_Splice_Rec_2070300,Human_Splice_Rec_2070312,Human_Splice_Rec_2070358,Human_Splice_Rec_2070362 107942 RMVar_ID_107942 Human_SNP_ID_678822496 m1A Human chr20 - 31569292 31569292 31569292 CCTGGAGCTGCCCTTGGCCTCCTGTGCCCTCTACCGGTGCACGCCTGTGTGGGCCCAGCCCCCAT CCTGGAGCTGCCCTTGGCCTCCTGTGCCCTCTGCCGGTGCACGCCTGTGTGGGCCCAGCCCCCAT T C HM13-AS1 Ensembl:ENSG00000230613 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:31569251..31569350 26863196 MeRIP-seq:(Medium) rs1249148009 Functional Loss SNV dbSNP153 33..33 33 - - - 107943 RMVar_ID_107943 Human_SNP_ID_678833853 m1A Human chr20 - 31605348 31605339 31605348 GGCGACTGGCTGAAACAGAATGGGCAAAGCGAAAAAAATGAGGTGGAAGCCCGAAGCAGATACGG GGCGACTGGCTGAAACAGAATGGGCAAAGCGA_________GGTGGAAGCCCGAAGCAGATACGG CTCATTTTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr20:31605301..31605458;chr20:31605301..31605552 26863196 MeRIP-seq:(Medium) rs1568818601 Functional Loss DEL dbSNP153 33..41 33 - - - 107944 RMVar_ID_107944 Human_SNP_ID_678833864 m1A Human chr20 - 31605348 31605348 31605348 GGCGACTGGCTGAAACAGAATGGGCAAAGCGAAAAAAATGAGGTGGAAGCCCGAAGCAGATACGG GGCGACTGGCTGAAACAGAATGGGCAAAGCGAGAAAAATGAGGTGGAAGCCCGAAGCAGATACGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr20:31605301..31605458;chr20:31605301..31605552 26863196 MeRIP-seq:(Medium) rs1485674140 Functional Loss SNV dbSNP153 33..33 33 - - - 107945 RMVar_ID_107945 Human_SNP_ID_678833903 m1A Human chr20 + 31605391 31605391 31605391 CATTCTGTTTCAGCCAGTCGCCAAGAATCATGAAAGTCGCCAGTGGCAGCACCGCCACCGCCGCC CATTCTGTTTCAGCCAGTCGCCAAGAATCATGGAAGTCGCCAGTGGCAGCACCGCCACCGCCGCC A G ID1 Ensembl:ENSG00000125968 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:31605376..31605400 26863196 MeRIP-seq:(Medium) rs567214145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62827,Human_RBP_ID_778980,Human_RBP_ID_923885,Human_RBP_ID_3960632,Human_RBP_ID_5148153,Human_RBP_ID_9331449,Human_RBP_ID_17282720,Human_RBP_ID_18423313,Human_RBP_ID_22452985 Human_miRNA_ID_2618342 RMVar_hsa_circ_78029,RMVar_hsa_circ_209202 107946 RMVar_ID_107946 Human_SNP_ID_678834059 m1A Human chr20 - 31605554 31605554 31605554 AGAGCAGCACGTTTACCTGCTGCTCGTCCAGCAGGGCAGGCAGGCGCGCCCCGGCGCCCCCGGCG AGAGCAGCACGTTTACCTGCTGCTCGTCCAGCGGGGCAGGCAGGCGCGCCCCGGCGCCCCCGGCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:31605376..31605625 32194978 MeRIP-seq:(Medium) rs1275791252 Functional Loss SNV dbSNP153 33..33 33 - - - 107947 RMVar_ID_107947 Human_SNP_ID_678834155 m1A Human chr20 - 31605702 31605702 31605702 CCAACTTCGGATTCCGAGTTCAGCTCCAACTGAAGGTCCCTGATGTAGTCGATGACGTGCTGGAG CCAACTTCGGATTCCGAGTTCAGCTCCAACTGCAGGTCCCTGATGTAGTCGATGACGTGCTGGAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:31605651..31605825 32194978 MeRIP-seq:(Medium) rs891708660 Functional Loss SNV dbSNP153 33..33 33 - - - 107948 RMVar_ID_107948 Human_SNP_ID_678834482 m1A Human chr20 + 31606124 31606124 31606124 TGAAGCGCCTCCCCCAGGGACCGGCGGACCCCAGCCATCCAGGGGGCAAGAGGAATTACGTGCTC TGAAGCGCCTCCCCCAGGGACCGGCGGACCCCTGCCATCCAGGGGGCAAGAGGAATTACGTGCTC A T ID1 Ensembl:ENSG00000125968 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:31606101..31606125 26863196 MeRIP-seq:(Medium) rs1449446260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924401,Human_RBP_ID_22080547,Human_RBP_ID_22452991,Human_RBP_ID_23005137,Human_RBP_ID_26489190 Human_Splice_Rec_2070368 RMVar_hsa_circ_115092,RMVar_hsa_circ_78029,RMVar_hsa_circ_209202,RMVar_hsa_circ_209203 107949 RMVar_ID_107949 Human_SNP_ID_678834513 m1A Human chr20 + 31606171 31606171 31606171 AAGAGGAATTACGTGCTCTGTGGGTCTCCCCCAACGCGCCTCGCCGGATCTGAGGGAGAACAAGA AAGAGGAATTACGTGCTCTGTGGGTCTCCCCCCACGCGCCTCGCCGGATCTGAGGGAGAACAAGA A C ID1 Ensembl:ENSG00000125968 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:31606014..31606263 26863196 MeRIP-seq:(Medium) rs570073683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831679,Human_RBP_ID_5263654,Human_RBP_ID_23004945 RMVar_hsa_circ_115092,RMVar_hsa_circ_78029,RMVar_hsa_circ_209202,RMVar_hsa_circ_209203 107950 RMVar_ID_107950 Human_SNP_ID_678834514 m1A Human chr20 + 31606171 31606171 31606171 AAGAGGAATTACGTGCTCTGTGGGTCTCCCCCAACGCGCCTCGCCGGATCTGAGGGAGAACAAGA AAGAGGAATTACGTGCTCTGTGGGTCTCCCCCTACGCGCCTCGCCGGATCTGAGGGAGAACAAGA A T ID1 Ensembl:ENSG00000125968 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:31606014..31606263 26863196 MeRIP-seq:(Medium) rs570073683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831679,Human_RBP_ID_5263654,Human_RBP_ID_23004945 RMVar_hsa_circ_115092,RMVar_hsa_circ_78029,RMVar_hsa_circ_209202,RMVar_hsa_circ_209203 107951 RMVar_ID_107951 Human_SNP_ID_678864278 m1A Human chr20 - 31721948 31721948 31721948 TGATCCCCATGGCAGCAGTAAAGCAAGCGCTGAGGGAGGCAGGCGACGAGTTTGAACTGCGGTAC TGATCCCCATGGCAGCAGTAAAGCAAGCGCTGGGGGAGGCAGGCGACGAGTTTGAACTGCGGTAC T C BCL2L1 Ensembl:ENSG00000171552 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31721898..31721978 26863196 MeRIP-seq:(Medium) rs901023938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62729,RMVar_hsa_circ_85932,RMVar_hsa_circ_209204 107952 RMVar_ID_107952 Human_SNP_ID_678864553 m1A Human chr20 - 31722896 31722896 31722896 GCAAGAGAGAGGGGGCTGGGCTCCCGGGTGGCAGGAGGCCGCGGCTGCGGAGCGGCCGCCCTCGA GCAAGAGAGAGGGGGCTGGGCTCCCGGGTGGCGGGAGGCCGCGGCTGCGGAGCGGCCGCCCTCGA T C BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31722848..31722972 26863196 MeRIP-seq:(Medium) rs1428567429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659307,Human_RBP_ID_5323187,Human_RBP_ID_22722893 107953 RMVar_ID_107953 Human_SNP_ID_678868804 m1A Human chr20 - 31739512 31739512 31739512 CAAGAGAAGCGTGGCCCGAAGCCCCTGCTCGCACCCTGCCCCGCCTAGGCGGCGACCGAGCACCG CAAGAGAAGCGTGGCCCGAAGCCCCTGCTCGCCCCCTGCCCCGCCTAGGCGGCGACCGAGCACCG T G lnc-BCL2L1-1 RNACentral:URS00008BFCB5 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:31739369..31739518 32194978 MeRIP-seq:(Medium) rs997919186 Functional Loss SNV dbSNP153 33..33 33 - - - 107954 RMVar_ID_107954 Human_SNP_ID_678883404 m1A Human chr20 - 31798452 31798452 31798452 ACTGCTGGGCTTTCTGGGCTTCTACCTCAGCCATTCTCTTCTCCAGCTCCTGCCGCTCTTTGGCT ACTGCTGGGCTTTCTGGGCTTCTACCTCAGCCTTTCTCTTCTCCAGCTCCTGCCGCTCTTTGGCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31798401..31798526 26863196 MeRIP-seq:(Medium) rs145356341 Functional Loss SNV dbSNP153 33..33 33 - - - 107955 RMVar_ID_107955 Human_SNP_ID_678883410 m1A Human chr20 + 31798472 31798472 31798472 TGGAGAAGAGAATGGCTGAGGTAGAAGCCCAGAAAGCCCAGCAGTTGGAGGAGGCCAGACTACAG TGGAGAAGAGAATGGCTGAGGTAGAAGCCCAGGAAGCCCAGCAGTTGGAGGAGGCCAGACTACAG A G TPX2 Ensembl:ENSG00000088325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:31798386..31798585;chr20:31798421..31798615 26863196 MeRIP-seq:(Medium) rs1166943553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62100,Human_RBP_ID_927327,Human_RBP_ID_1594563,Human_RBP_ID_1927544,Human_RBP_ID_6988347,Human_RBP_ID_9388905,Human_RBP_ID_17658859,Human_RBP_ID_26342396 Human_Splice_Rec_2070443,Human_Splice_Rec_2070477 Human_miRNA_ID_1158684,Human_miRNA_ID_2555326,Human_miRNA_ID_2555327 RMVar_hsa_circ_83141,RMVar_hsa_circ_209205,RMVar_hsa_circ_111353,RMVar_hsa_circ_209207,RMVar_hsa_circ_100485,RMVar_hsa_circ_64256,RMVar_hsa_circ_113022,RMVar_hsa_circ_209208,RMVar_hsa_circ_78424,RMVar_hsa_circ_209211,RMVar_hsa_circ_209213,RMVar_hsa_circ_81307,RMVar_hsa_circ_209215,RMVar_hsa_circ_110638,RMVar_hsa_circ_113295,RMVar_hsa_circ_209216,RMVar_hsa_circ_209218,RMVar_hsa_circ_93185,RMVar_hsa_circ_123721,RMVar_hsa_circ_76955,RMVar_hsa_circ_209220,RMVar_hsa_circ_335845,RMVar_hsa_circ_209221,RMVar_hsa_circ_209225,RMVar_hsa_circ_90183,RMVar_hsa_circ_46490,RMVar_hsa_circ_109737,RMVar_hsa_circ_209227,RMVar_hsa_circ_322821,RMVar_hsa_circ_209229,RMVar_hsa_circ_209230,RMVar_hsa_circ_79257,RMVar_hsa_circ_123124,RMVar_hsa_circ_209232,RMVar_hsa_circ_209233,RMVar_hsa_circ_101668,RMVar_hsa_circ_104468,RMVar_hsa_circ_209235,RMVar_hsa_circ_209236 107956 RMVar_ID_107956 Human_SNP_ID_678921199 m1A Human chr20 + 31950383 31950383 31950383 CTCGATTCTGATTCCTTTTAGTGTCCAGGTCCACAATCTGAAAACCACAGGGACAGGAGGGAACT CTCGATTCTGATTCCTTTTAGTGTCCAGGTCCGCAATCTGAAAACCACAGGGACAGGAGGGAACT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:31950326..31950400 26863196 MeRIP-seq:(Medium) rs139473332 Functional Loss SNV dbSNP153 33..33 33 - - - 107957 RMVar_ID_107957 Human_SNP_ID_678961355 m1A Human chr20 + 32109769 32109769 32109769 CAAGATGGCGACGGCGATGGTGAGTGAAGGAGACTCCGGGAGCGGGAGCTGGAGCGGGGCCCTCC CAAGATGGCGACGGCGATGGTGAGTGAAGGAGCCTCCGGGAGCGGGAGCTGGAGCGGGGCCCTCC A C TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32109765..32109871 26863196 MeRIP-seq:(Medium) rs755429903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422847,Human_RBP_ID_19106138 RMVar_hsa_circ_96443,RMVar_hsa_circ_209247 107958 RMVar_ID_107958 Human_SNP_ID_678961359 m1A Human chr20 - 32109786 32109774 32109786 AGATCCTGGGATACCCCGGAGGGCCCCGCTCCAGCTCCCGCTCCCGGAGTCTCCTTCACTCACCA AGATCCTGGGATACCCCGGAGGGCCCCGCTCC____________CGGAGTCTCCTTCACTCACCA GGGAGCGGGAGCT G lnc-PLAGL2-6 RNACentral:URS00008B7F2E lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:32109747..32109890 26863196 MeRIP-seq:(Medium) rs1472817402 Functional Loss DEL dbSNP153 33..44 33 - - - 107959 RMVar_ID_107959 Human_SNP_ID_678961436 m1A Human chr20 + 32109967 32109967 32109967 CTCAGGCTTGTGAAGGCCCCGAGTTTTGGGGGAGGCGCCGTTTCGGAGGAAGACCTCGGCTGCTG CTCAGGCTTGTGAAGGCCCCGAGTTTTGGGGGTGGCGCCGTTTCGGAGGAAGACCTCGGCTGCTG A T TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32109965..32110312 26863196 MeRIP-seq:(Medium) rs1314453762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26787890 Human_Splice_Rec_2071279,Human_Splice_Rec_2071313 RMVar_hsa_circ_96443,RMVar_hsa_circ_209247 107960 RMVar_ID_107960 Human_SNP_ID_678971765 m1A Human chr20 + 32149751 32149751 32149751 TGCTGGGCTCAGGCATTCAGCTGTTCTGTATGATCCTCATCGTCATCTGTGAGTGTGCCCAGCGG TGCTGGGCTCAGGCATTCAGCTGTTCTGTATGGTCCTCATCGTCATCTGTGAGTGTGCCCAGCGG A G TM9SF4 Ensembl:ENSG00000101337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:32149651..32149775 32194978 MeRIP-seq:(Medium) rs1179609643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1927591,Human_RBP_ID_8530224,Human_RBP_ID_22766957 Human_Splice_Rec_2071243,Human_Splice_Rec_2071297 RMVar_hsa_circ_107583,RMVar_hsa_circ_90758,RMVar_hsa_circ_24206,RMVar_hsa_circ_209249,RMVar_hsa_circ_209250,RMVar_hsa_circ_86677,RMVar_hsa_circ_102878,RMVar_hsa_circ_108766,RMVar_hsa_circ_115966,RMVar_hsa_circ_209260,RMVar_hsa_circ_125449,RMVar_hsa_circ_124233,RMVar_hsa_circ_209264,RMVar_hsa_circ_209265,RMVar_hsa_circ_209263,RMVar_hsa_circ_118637,RMVar_hsa_circ_209267,RMVar_hsa_circ_102116,RMVar_hsa_circ_209266,RMVar_hsa_circ_372024,RMVar_hsa_circ_117142,RMVar_hsa_circ_209269,RMVar_hsa_circ_209271,RMVar_hsa_circ_81325,RMVar_hsa_circ_209272,RMVar_hsa_circ_209270,RMVar_hsa_circ_209268 107961 RMVar_ID_107961 Human_SNP_ID_678986122 m1A Human chr20 - 32207980 32207980 32207980 ATCCCCGGGAGCGGCAGAAGCAGCAGCAGGAAAGACACGCTCAGCGGCCGTGCCCACGCGGCGGC ATCCCCGGGAGCGGCAGAAGCAGCAGCAGGAAGGACACGCTCAGCGGCCGTGCCCACGCGGCGGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:32207930..32208038 26863196 MeRIP-seq:(Medium) rs780725234 Functional Loss SNV dbSNP153 33..33 33 - - - 107962 RMVar_ID_107962 Human_SNP_ID_678986123 m1A Human chr20 - 32207980 32207980 32207980 ATCCCCGGGAGCGGCAGAAGCAGCAGCAGGAAAGACACGCTCAGCGGCCGTGCCCACGCGGCGGC ATCCCCGGGAGCGGCAGAAGCAGCAGCAGGAACGACACGCTCAGCGGCCGTGCCCACGCGGCGGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:32207930..32208038 26863196 MeRIP-seq:(Medium) rs780725234 Functional Loss SNV dbSNP153 33..33 33 - - - 107963 RMVar_ID_107963 Human_SNP_ID_678993064 m1A Human chr20 + 32237466 32237466 32237466 GTCATGAAGGAGGGAGGGAGCACATTCCTGGCAGAGAAAACAGCACGTGCAAAGGCCCCGAGACT GTCATGAAGGAGGGAGGGAGCACATTCCTGGCGGAGAAAACAGCACGTGCAAAGGCCCCGAGACT A G POFUT1 Ensembl:ENSG00000101346 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:32237416..32237574 26863196 MeRIP-seq:(Medium) rs543776814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_561307,Human_RBP_ID_6989087,Human_RBP_ID_8204902,Human_RBP_ID_18321396,Human_RBP_ID_23899251 Human_miRNA_ID_1311056 107964 RMVar_ID_107964 Human_SNP_ID_679004128 m1A Human chr20 - 32282106 32282104 32282106 CCCTCTAAAATTCACTGCCACAAAGAGGCCAGAGTGATTTTTTTAAAAAACAAAAATAGATCATG CCCTCTAAAATTCACTGCCACAAAGAGGCCAG__TGATTTTTTTAAAAAACAAAAATAGATCATG ACT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32282104..32282320 26863196 MeRIP-seq:(Medium) rs1394086891 Functional Loss DEL dbSNP153 33..34 33 - - - 107965 RMVar_ID_107965 Human_SNP_ID_679011199 m1A Human chr20 + 32311144 32311144 32311144 GAAAGAGAAAAAGATGGAGGACCTGCGGCGGGAGAAGGATGCTGCCGAGATGCTGGGCGCCAAGA GAAAGAGAAAAAGATGGAGGACCTGCGGCGGGGGAAGGATGCTGCCGAGATGCTGGGCGCCAAGA A G KIF3B Ensembl:ENSG00000101350 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:32310989..32311175 26863196 MeRIP-seq:(Medium) rs892427720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1025317,Human_RBP_ID_5528973,Human_RBP_ID_19106153,Human_RBP_ID_27484345 Human_Splice_Rec_2071367 RMVar_hsa_circ_44469,RMVar_hsa_circ_319241,RMVar_hsa_circ_346622,RMVar_hsa_circ_209281 107966 RMVar_ID_107966 Human_SNP_ID_679018916 m1A Human chr20 + 32341035 32341027 32341035 CTGAGTAGCTAGAATTACAGGCATGCGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGA CTGAGTAGCTAGAATTACAGGCATG________CGCCCGGCTAATTTTTGTATTTTTAGTAGAGA GCGCCACCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:32340999..32341112 26863196 MeRIP-seq:(Medium) rs923734002 Functional Loss DEL dbSNP153 26..33 33 - - - 107967 RMVar_ID_107967 Human_SNP_ID_679022829 m1A Human chr20 - 32358531 32358522 32358531 GCGCCCGCGCTGCGTCAGTCGCCCACGGCGGCAGCGGCGGCTGCCCCGCGATCGCTAAGGAATGC GCGCCCGCGCTGCGTCAGTCGCCCACGGCGGC_________TGCCCCGCGATCGCTAAGGAATGC AGCCGCCGCT A lnc-NOL4L-2 RNACentral:URS0000D58B70 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:32358393..32358692 32194978 MeRIP-seq:(Medium) rs989489003 Functional Loss DEL dbSNP153 33..41 33 - - - 107968 RMVar_ID_107968 Human_SNP_ID_679022840 m1A Human chr20 + 32358553 32358553 32358553 CAGCCGCCGCTGCCGCCGTGGGCGACTGACGCAGCGCGGGCGCGTGGAGCCGCCGCCGCCCCTCC CAGCCGCCGCTGCCGCCGTGGGCGACTGACGCTGCGCGGGCGCGTGGAGCCGCCGCCGCCCCTCC A T ASXL1 Ensembl:ENSG00000171456 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:32358391..32358595 26863410 MeRIP-seq:(Medium) rs886056587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659316,Human_RBP_ID_22533638 Clinvar_Rec_696 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 107969 RMVar_ID_107969 Human_SNP_ID_679022887 m1A Human chr20 + 32358685 32358658 32358686 CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCACCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC CTCGCG____________________________CGCCGCCGCCGCCCCAGCCCCGCGCCACCGC GCGCCGCCGCTGCCACGCGCCCCCCCCAC G ASXL1 Ensembl:ENSG00000171456 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr20:32358417..32358778;chr20:32358599..32358774 26863196 MeRIP-seq:(Medium) rs954034889 Functional Loss DEL dbSNP153 7..34 33 - - - Human_RBP_ID_4641116,Human_RBP_ID_5384845,Human_RBP_ID_9331799,Human_RBP_ID_22533639 Human_miRNA_ID_2387528,Human_miRNA_ID_2389001,Human_miRNA_ID_2400150,Human_miRNA_ID_2686409,Human_miRNA_ID_3031213 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 107970 RMVar_ID_107970 Human_SNP_ID_679022911 m1A Human chr20 + 32358685 32358685 32358685 CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCACCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCCCCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC A C ASXL1 Ensembl:ENSG00000171456 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr20:32358417..32358778;chr20:32358599..32358774 26863196 MeRIP-seq:(Medium) rs1020071543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4641116,Human_RBP_ID_5384845,Human_RBP_ID_9331799,Human_RBP_ID_22533639 Human_miRNA_ID_2387528,Human_miRNA_ID_2389001,Human_miRNA_ID_2400150,Human_miRNA_ID_2686409,Human_miRNA_ID_3031213 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 107971 RMVar_ID_107971 Human_SNP_ID_679022912 m1A Human chr20 + 32358685 32358685 32358685 CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCACCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCGCCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC A G ASXL1 Ensembl:ENSG00000171456 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr20:32358417..32358778;chr20:32358599..32358774 26863196 MeRIP-seq:(Medium) rs1020071543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4641116,Human_RBP_ID_5384845,Human_RBP_ID_9331799,Human_RBP_ID_22533639 Human_miRNA_ID_2387528,Human_miRNA_ID_2389001,Human_miRNA_ID_2400150,Human_miRNA_ID_2686409,Human_miRNA_ID_3031213 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 107972 RMVar_ID_107972 Human_SNP_ID_679024460 m1A Human chr20 - 32363805 32363800 32363806 GCAAATACACACACTCCCTCTCACCCACTCTGACTCTTTCTCTCCTGCTATGTGTTGTCACCAGC GCAAATACACACACTCCCTCTCACCCACTCT______TTCTCTCCTGCTATGTGTTGTCACCAGC AAGAGTC A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:32363803..32363904 26863196 MeRIP-seq:(Medium) rs571684652 Functional Loss DEL dbSNP153 32..37 33 - - - 107973 RMVar_ID_107973 Human_SNP_ID_679024737 m1A Human chr20 + 32364923 32364923 32364923 TTTGAGGAAAGCAGGACTGGATGGAGGGATAAATATTAAGAGGCTGTTGTGTTGGGTCAGGTAAG TTTGAGGAAAGCAGGACTGGATGGAGGGATAAGTATTAAGAGGCTGTTGTGTTGGGTCAGGTAAG A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:32364921..32365147 26863196 MeRIP-seq:(Medium) rs991411921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17142790 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 107974 RMVar_ID_107974 Human_SNP_ID_679041356 m1A Human chr20 + 32430041 32430041 32430041 AGGACCCTGCCCCGCTCCTGAGAGGCTTCCGGAAGCCAGCCACAGGTGAGTGGCGTGGCACTTAT AGGACCCTGCCCCGCTCCTGAGAGGCTTCCGGCAGCCAGCCACAGGTGAGTGGCGTGGCACTTAT A C ASXL1 Ensembl:ENSG00000171456 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:32429810..32430868 32194978 MeRIP-seq:(Medium) rs761932590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5384855,Human_RBP_ID_19005297 Human_Splice_Rec_2071395,Human_Splice_Rec_2071421,Human_Splice_Rec_2071445,Human_Splice_Rec_2071485,Human_Splice_Rec_2071589,Human_Splice_Rec_2071651,Human_Splice_Rec_2071655 RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209308,RMVar_hsa_circ_112463,RMVar_hsa_circ_48381,RMVar_hsa_circ_209310 107975 RMVar_ID_107975 Human_SNP_ID_679042167 m1A Human chr20 + 32433334 32433334 32433334 AGAGTCATTGCAGCAGAACGTGGGCCAGGAGGAGGCTGAAATCAAAAGTGGCTTGTGTGTCCCAG AGAGTCATTGCAGCAGAACGTGGGCCAGGAGGCGGCTGAAATCAAAAGTGGCTTGTGTGTCCCAG A C ASXL1 Ensembl:ENSG00000171456 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:32433266..32433555 26863196 MeRIP-seq:(Medium) rs1434163063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63174,Human_RBP_ID_923898,Human_RBP_ID_5528977,Human_RBP_ID_8857319,Human_RBP_ID_18167478,Human_RBP_ID_18412905,Human_RBP_ID_22080579,Human_RBP_ID_23004947,Human_RBP_ID_24546644,Human_RBP_ID_26342399 Human_Splice_Rec_2071402,Human_Splice_Rec_2071428,Human_Splice_Rec_2071452,Human_Splice_Rec_2071492,Human_Splice_Rec_2071536,Human_Splice_Rec_2071596,Human_Splice_Rec_2071650,Human_Splice_Rec_2071668,Human_Splice_Rec_2071670 RMVar_hsa_circ_107754,RMVar_hsa_circ_209308,RMVar_hsa_circ_112463,RMVar_hsa_circ_105191,RMVar_hsa_circ_115277,RMVar_hsa_circ_209310,RMVar_hsa_circ_209311,RMVar_hsa_circ_209312 107976 RMVar_ID_107976 Human_SNP_ID_679042341 m1A Human chr20 - 32433727 32433727 32433727 CCTTGGGTTCCTGATCCACAGTTTCCTGAGGCAGGCTAGGAATTCTGTCTGGAGATGCAGAGGCA CCTTGGGTTCCTGATCCACAGTTTCCTGAGGCGGGCTAGGAATTCTGTCTGGAGATGCAGAGGCA T C lnc-NOL4L-3 RNACentral:URS0000D5A3C3 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:32433676..32433814 26863196 MeRIP-seq:(Medium) rs752413007 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 107977 RMVar_ID_107977 Human_SNP_ID_679042402 m1A Human chr20 + 32433867 32433867 32433867 AGTCCTTTCGTAACACAATTGAAAGTGTTCACACCGAAAAGCCACAGCCCACTAAAGAGGAGCCC AGTCCTTTCGTAACACAATTGAAAGTGTTCACGCCGAAAAGCCACAGCCCACTAAAGAGGAGCCC A G ASXL1 Ensembl:ENSG00000171456 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:32433816..32433936 26863196 MeRIP-seq:(Medium) rs1185741428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925478,Human_RBP_ID_5528982,Human_RBP_ID_17969526,Human_RBP_ID_22081292 Human_Splice_Rec_2071403,Human_Splice_Rec_2071429,Human_Splice_Rec_2071453,Human_Splice_Rec_2071493,Human_Splice_Rec_2071537,Human_Splice_Rec_2071597,Human_Splice_Rec_2071671 RMVar_hsa_circ_107754,RMVar_hsa_circ_209308,RMVar_hsa_circ_112463,RMVar_hsa_circ_105191,RMVar_hsa_circ_115277,RMVar_hsa_circ_209310,RMVar_hsa_circ_209311,RMVar_hsa_circ_209312 107978 RMVar_ID_107978 Human_SNP_ID_679043289 m1A Human chr20 - 32436035 32436035 32436035 CTAGGGGCAAGCTACCCTGCAGCAACTGCATCACAAGTGGGTTAGTGGCCTCCACTGAGGACCCA CTAGGGGCAAGCTACCCTGCAGCAACTGCATCGCAAGTGGGTTAGTGGCCTCCACTGAGGACCCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:32435985..32436085 32194978 MeRIP-seq:(Medium) rs1454365420 Functional Loss SNV dbSNP153 33..33 33 - - - 107979 RMVar_ID_107979 Human_SNP_ID_679043504 m1A Human chr20 + 32436501 32436501 32436501 AGTAATTCAAATGCTGCTCCAGGAAAGAGCCCAGGAGATCTTACTACCTCGAGAACACCTCGTTT AGTAATTCAAATGCTGCTCCAGGAAAGAGCCCGGGAGATCTTACTACCTCGAGAACACCTCGTTT A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:32436451..32436603 26863196 MeRIP-seq:(Medium) rs755293418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3646005,Human_RBP_ID_17969534,Human_RBP_ID_18167949 Human_miRNA_ID_1915286,Human_miRNA_ID_1917735,Human_miRNA_ID_1920189,Human_miRNA_ID_1922646,Human_miRNA_ID_1925100,Human_miRNA_ID_1927550,Human_miRNA_ID_1930000,Human_miRNA_ID_1932449,Human_miRNA_ID_2041625,Human_miRNA_ID_2168933,Human_miRNA_ID_2170456,Human_miRNA_ID_2555330,Human_miRNA_ID_2630275,Human_miRNA_ID_2791116,Human_miRNA_ID_3020603,Human_miRNA_ID_3126135 RMVar_hsa_circ_107754,RMVar_hsa_circ_209308,RMVar_hsa_circ_105191,RMVar_hsa_circ_115277,RMVar_hsa_circ_209311,RMVar_hsa_circ_209312 107980 RMVar_ID_107980 Human_SNP_ID_679047622 m1A Human chr20 - 32452393 32452393 32452393 GCCCTGGACAAGCAGCACTCGCGGGACTCCGCAGCCATCACCCACTCCACCTACTCACTGCCAGC GCCCTGGACAAGCAGCACTCGCGGGACTCCGCCGCCATCACCCACTCCACCTACTCACTGCCAGC T G NOL4L Ensembl:ENSG00000197183 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:32452214..32452471 26863196 MeRIP-seq:(Medium) rs748432678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17283385 Human_Splice_Rec_2071684,Human_Splice_Rec_2071704,Human_Splice_Rec_2071716 RMVar_hsa_circ_3460,RMVar_hsa_circ_112550,RMVar_hsa_circ_209314,RMVar_hsa_circ_78138,RMVar_hsa_circ_209313 107981 RMVar_ID_107981 Human_SNP_ID_679048295 m1A Human chr20 + 32454438 32454438 32454438 AAAGGGAGAGGGAACCGGATCCGGCCTCCCCCAGCAGTCTCCTGTCCTCCAGTAGAGAAGGGCTC AAAGGGAGAGGGAACCGGATCCGGCCTCCCCCCGCAGTCTCCTGTCCTCCAGTAGAGAAGGGCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32454435..32454666 26863196 MeRIP-seq:(Medium) rs554463098 Functional Loss SNV dbSNP153 33..33 33 - - - 107982 RMVar_ID_107982 Human_SNP_ID_679055857 m1A Human chr20 - 32482799 32482799 32482799 TGGGGATGTGAGGACGGGAAGCGTTGAGTGTCAGGGAGGGGTTCCCCGGCGCGGCGCGGGGAGTT TGGGGATGTGAGGACGGGAAGCGTTGAGTGTCGGGGAGGGGTTCCCCGGCGCGGCGCGGGGAGTT T C NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:32482797..32482988 26863196 MeRIP-seq:(Medium) rs959664354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3654147,Human_RBP_ID_8113304,Human_RBP_ID_18463302,Human_RBP_ID_18494937,Human_RBP_ID_22417553,Human_RBP_ID_22701024 RMVar_hsa_circ_209314,RMVar_hsa_circ_78138,RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317 107983 RMVar_ID_107983 Human_SNP_ID_679056127 m1A Human chr20 + 32483631 32483631 32483631 GGGAGGGGGCACCGGGCACGGGGAGGCGGGAGAGGGGGCGGGACCGGGCACGGGGCGGGGGCGGG GGGAGGGGGCACCGGGCACGGGGAGGCGGGAGGGGGGGCGGGACCGGGCACGGGGCGGGGGCGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:32483481..32483644 26863196 MeRIP-seq:(Medium) rs1489490369 Functional Loss SNV dbSNP153 33..33 33 - - - 107984 RMVar_ID_107984 Human_SNP_ID_679056229 m1A Human chr20 - 32483888 32483888 32483888 CGCTCCCCACCGAAGCGCACGGCGGCGCGTCCAGCGCGCCCTTATCCCCCCCTACCTGGCCCAGC CGCTCCCCACCGAAGCGCACGGCGGCGCGTCCTGCGCGCCCTTATCCCCCCCTACCTGGCCCAGC T A NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:32483810..32483985 26863196 MeRIP-seq:(Medium) rs1354477381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317 107985 RMVar_ID_107985 Human_SNP_ID_679056230 m1A Human chr20 - 32483888 32483888 32483888 CGCTCCCCACCGAAGCGCACGGCGGCGCGTCCAGCGCGCCCTTATCCCCCCCTACCTGGCCCAGC CGCTCCCCACCGAAGCGCACGGCGGCGCGTCCCGCGCGCCCTTATCCCCCCCTACCTGGCCCAGC T G NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:32483810..32483985 26863196 MeRIP-seq:(Medium) rs1354477381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317 107986 RMVar_ID_107986 Human_SNP_ID_679064602 m1A Human chr20 - 32515505 32515505 32515505 CTCTCAGTGTGCACCCACTTATTGAATCCAGAACACCTGGGGCTCCTCACTGCTGAAAAGCTTGC CTCTCAGTGTGCACCCACTTATTGAATCCAGAGCACCTGGGGCTCCTCACTGCTGAAAAGCTTGC T C NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:32515459..32515574 26863196 MeRIP-seq:(Medium) rs1209600284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26314,RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317,RMVar_hsa_circ_209319,RMVar_hsa_circ_304872 107987 RMVar_ID_107987 Human_SNP_ID_679064824 m1A Human chr20 - 32516387 32516386 32516388 TGTTTCCTGAGCCTGGGGACTGCACCGCACACAGTTTCCTCACGTTCCCCACCCGGATAGCATGC TGTTTCCTGAGCCTGGGGACTGCACCGCACA__GTTTCCTCACGTTCCCCACCCGGATAGCATGC CTG C NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32516347..32516493 26863196 MeRIP-seq:(Medium) rs573643514 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_26314,RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317,RMVar_hsa_circ_209319,RMVar_hsa_circ_304872 107988 RMVar_ID_107988 Human_SNP_ID_679065872 m1A Human chr20 - 32520396 32520396 32520396 TGAGACGTGTGCATGCATCCTCCCACCCACATACCTGTTAATGATACATCTTCCCTGGTGCTTGT TGAGACGTGTGCATGCATCCTCCCACCCACATCCCTGTTAATGATACATCTTCCCTGGTGCTTGT T G NOL4L Ensembl:ENSG00000197183 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:32520345..32520531 26863196 MeRIP-seq:(Medium) rs981390400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17086429 RMVar_hsa_circ_26314,RMVar_hsa_circ_84429,RMVar_hsa_circ_341120,RMVar_hsa_circ_28052,RMVar_hsa_circ_209317,RMVar_hsa_circ_209319,RMVar_hsa_circ_304872 107989 RMVar_ID_107989 Human_SNP_ID_679127495 m1A Human chr20 - 32762635 32762621 32762636 GGCGGAGCCGCGGGTCGGGGCTGGCTGGCGGGAGGCCGGCTGGCGGCCGTGCAGGGCGCTGGGCT GGCGGAGCCGCGGGTCGGGGCTGGCTGGCGG_______________CCGTGCAGGGCGCTGGGCT GCCGCCAGCCGGCCTC G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:32762401..32762638 26863410 MeRIP-seq:(Medium) rs1174293028 Functional Loss DEL dbSNP153 32..46 33 - - - 107990 RMVar_ID_107990 Human_SNP_ID_679127608 m1A Human chr20 + 32762948 32762948 32762948 CGCGGGGGACATACGTCTGACGGGGACCGGAGATACTAGAGGAAGGGACGCGTCTGCTGCCTCCA CGCGGGGGACATACGTCTGACGGGGACCGGAGTTACTAGAGGAAGGGACGCGTCTGCTGCCTCCA A T DNMT3B Ensembl:ENSG00000088305 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:32762918..32763002 26863196 MeRIP-seq:(Medium) rs1568812631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5323210,Human_RBP_ID_8234794,Human_RBP_ID_22722232 107991 RMVar_ID_107991 Human_SNP_ID_679142822 m1A Human chr20 + 32820003 32820003 32820003 AGACGAAGACGGAACCGGAGCCGGTTGCGGGCAGTGGACGCGGTTCTGCCGAGAGCCGGTGAGCC AGACGAAGACGGAACCGGAGCCGGTTGCGGGCGGTGGACGCGGTTCTGCCGAGAGCCGGTGAGCC A G MAPRE1 Ensembl:ENSG00000101367 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:32819953..32820079 26863196 MeRIP-seq:(Medium) rs1486395873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63519,Human_RBP_ID_244802,Human_RBP_ID_561508,Human_RBP_ID_4641516,Human_RBP_ID_5503180,Human_RBP_ID_6989948,Human_RBP_ID_9388938,Human_RBP_ID_14067276,Human_RBP_ID_18422851,Human_RBP_ID_22080596,Human_RBP_ID_23899785,Human_RBP_ID_24546740,Human_RBP_ID_26342401,Human_RBP_ID_27019401 Human_Splice_Rec_2072175 107992 RMVar_ID_107992 Human_SNP_ID_679147447 m1A Human chr20 + 32836819 32836819 32836819 CTTGTTGCTCCAGCTCTGAATAAACCGAAGAAACCTCTCACTTCTAGCAGTGCAGGTAAAAAAAC CTTGTTGCTCCAGCTCTGAATAAACCGAAGAAGCCTCTCACTTCTAGCAGTGCAGGTAAAAAAAC A G MAPRE1 Ensembl:ENSG00000101367 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:32836770..32836884 26863196 MeRIP-seq:(Medium) rs1381348824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927199,Human_RBP_ID_1594914,Human_RBP_ID_1927864,Human_RBP_ID_8853595,Human_RBP_ID_9388947,Human_RBP_ID_14067511,Human_RBP_ID_17280997,Human_RBP_ID_17969600,Human_RBP_ID_22453702,Human_RBP_ID_27484528,Human_RBP_ID_27700805 Human_Splice_Rec_2072181 RMVar_hsa_circ_7681,RMVar_hsa_circ_365126,RMVar_hsa_circ_283483,RMVar_hsa_circ_102014,RMVar_hsa_circ_331074,RMVar_hsa_circ_209340,RMVar_hsa_circ_209341,RMVar_hsa_circ_323368 107993 RMVar_ID_107993 Human_SNP_ID_679287353 m1A Human chr20 + 33387437 33387437 33387437 CAGCTTGCTGGCCCGACTCAGCAACAGCCAGCAGCCGGGGAAGGTCCCGGTAGGCATCAGGACCA CAGCTTGCTGGCCCGACTCAGCAACAGCCAGCTGCCGGGGAAGGTCCCGGTAGGCATCAGGACCA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33387386..33387487 32194978 MeRIP-seq:(Medium) rs774156149 Functional Loss SNV dbSNP153 33..33 33 - - - 107994 RMVar_ID_107994 Human_SNP_ID_679287729 m1A Human chr20 - 33388620 33388618 33388620 GAAAGAGAGGGAGAGGGAGACAGTGGAAAGAGAGGGAGACGGAGACTGTGGGGAGAGGGAGAAGG GAAAGAGAGGGAGAGGGAGACAGTGGAAAGAG__GGAGACGGAGACTGTGGGGAGAGGGAGAAGG CCT C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33388592..33388691 26863196 MeRIP-seq:(Medium) rs1336753642 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23900220 RMVar_hsa_circ_31033,RMVar_hsa_circ_78082,RMVar_hsa_circ_209378,RMVar_hsa_circ_301190,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_25879,RMVar_hsa_circ_304833,RMVar_hsa_circ_309551,RMVar_hsa_circ_362411,RMVar_hsa_circ_375733,RMVar_hsa_circ_301731,RMVar_hsa_circ_54544,RMVar_hsa_circ_209393,RMVar_hsa_circ_209394,RMVar_hsa_circ_209399,RMVar_hsa_circ_83443,RMVar_hsa_circ_320012,RMVar_hsa_circ_42466,RMVar_hsa_circ_329843 107995 RMVar_ID_107995 Human_SNP_ID_679287734 m1A Human chr20 - 33388641 33388641 33388641 GGGCATCAGAGGGAGACCGTGGAAAGAGAGGGAGAGGGAGACAGTGGAAAGAGAGGGAGACGGAG GGGCATCAGAGGGAGACCGTGGAAAGAGAGGGGGAGGGAGACAGTGGAAAGAGAGGGAGACGGAG T C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33388590..33388696 26863196 MeRIP-seq:(Medium) rs373963914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23900220 RMVar_hsa_circ_31033,RMVar_hsa_circ_78082,RMVar_hsa_circ_209378,RMVar_hsa_circ_301190,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_25879,RMVar_hsa_circ_304833,RMVar_hsa_circ_309551,RMVar_hsa_circ_362411,RMVar_hsa_circ_375733,RMVar_hsa_circ_301731,RMVar_hsa_circ_54544,RMVar_hsa_circ_209393,RMVar_hsa_circ_209394,RMVar_hsa_circ_209399,RMVar_hsa_circ_83443,RMVar_hsa_circ_320012,RMVar_hsa_circ_42466,RMVar_hsa_circ_329843 107996 RMVar_ID_107996 Human_SNP_ID_679289309 m1A Human chr20 - 33394043 33394043 33394043 TCCATTCAGGCAGATGTGATTCTCCTTGTCACATGCTCTATCAGGTGCGAATTTGTTCTTTTCCT TCCATTCAGGCAGATGTGATTCTCCTTGTCACGTGCTCTATCAGGTGCGAATTTGTTCTTTTCCT T C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs291700 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5384896,Human_RBP_ID_9347994,Human_RBP_ID_19005357,Human_RBP_ID_19107971,Human_RBP_ID_25626906 Human_Splice_Rec_2072774,Human_Splice_Rec_2072775,Human_Splice_Rec_2072802,Human_Splice_Rec_2072803,Human_Splice_Rec_2072828,Human_Splice_Rec_2072829,Human_Splice_Rec_2072854,Human_Splice_Rec_2072855,Human_Splice_Rec_2072882,Human_Splice_Rec_2072883,Human_Splice_Rec_2072948,Human_Splice_Rec_2072949,Human_Splice_Rec_2072960,Human_Splice_Rec_2072961 GWAS_ID_14801,GWAS_ID_14802,GWAS_ID_14803,GWAS_ID_14804,GWAS_ID_14805,GWAS_ID_14806,GWAS_ID_14807,GWAS_ID_14808,GWAS_ID_14809,GWAS_ID_14810,GWAS_ID_14811,GWAS_ID_14812,GWAS_ID_14813,GWAS_ID_14814,GWAS_ID_14815,GWAS_ID_14816,GWAS_ID_14817,GWAS_ID_14818,GWAS_ID_14819,GWAS_ID_14820,GWAS_ID_14821,GWAS_ID_14822,GWAS_ID_14823,GWAS_ID_14824,GWAS_ID_14825,GWAS_ID_14826,GWAS_ID_14827,GWAS_ID_14828,GWAS_ID_14829,GWAS_ID_14830,GWAS_ID_14831,GWAS_ID_14832,GWAS_ID_14833,GWAS_ID_14834,GWAS_ID_14835,GWAS_ID_14836,GWAS_ID_14837,GWAS_ID_14838,GWAS_ID_14839,GWAS_ID_14840,GWAS_ID_14841,GWAS_ID_14842,GWAS_ID_14843,GWAS_ID_14844,GWAS_ID_14845,GWAS_ID_14846,GWAS_ID_14847,GWAS_ID_14848,GWAS_ID_14849,GWAS_ID_14850,GWAS_ID_14851 RMVar_hsa_circ_31033,RMVar_hsa_circ_78082,RMVar_hsa_circ_209378,RMVar_hsa_circ_301190,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_25879,RMVar_hsa_circ_375733,RMVar_hsa_circ_301731,RMVar_hsa_circ_54544,RMVar_hsa_circ_209393,RMVar_hsa_circ_209394,RMVar_hsa_circ_209399,RMVar_hsa_circ_83443,RMVar_hsa_circ_209403,RMVar_hsa_circ_42466,RMVar_hsa_circ_300574,RMVar_hsa_circ_300873,RMVar_hsa_circ_319670,RMVar_hsa_circ_42662,RMVar_hsa_circ_209402,RMVar_hsa_circ_209404,RMVar_hsa_circ_114957 107997 RMVar_ID_107997 Human_SNP_ID_679290987 m1A Human chr20 - 33401446 33401446 33401446 GCCGGCAGAACTTACGCTGCGGGACCCCGGGCACTGTTGCTGCTGCGGGAGGTGAGCAGCGCGGC GCCGGCAGAACTTACGCTGCGGGACCCCGGGCCCTGTTGCTGCTGCGGGAGGTGAGCAGCGCGGC T G CDK5RAP1 Ensembl:ENSG00000101391 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:33401316..33401452;chr20:33401369..33401453 26863196 MeRIP-seq:(Medium) rs906307604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_779822,Human_RBP_ID_4659734,Human_RBP_ID_9331477,Human_RBP_ID_18422855,Human_RBP_ID_19005359,Human_RBP_ID_22080602,Human_RBP_ID_23119668 Human_Splice_Rec_2072773,Human_Splice_Rec_2072787,Human_Splice_Rec_2072797,Human_Splice_Rec_2072823,Human_Splice_Rec_2072849,Human_Splice_Rec_2072877,Human_Splice_Rec_2072911,Human_Splice_Rec_2072923,Human_Splice_Rec_2072931,Human_Splice_Rec_2072945,Human_Splice_Rec_2072959,Human_Splice_Rec_2072969 107998 RMVar_ID_107998 Human_SNP_ID_679293295 m1A Human chr20 + 33411274 33411274 33411274 TCCTATCCAAGCTCCCTCTCCATCCCACACACACTCTGGACTTAACTCAGCATCTTGCTCCAGCC TCCTATCCAAGCTCCCTCTCCATCCCACACACCCTCTGGACTTAACTCAGCATCTTGCTCCAGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33411232..33411379 26863196 MeRIP-seq:(Medium) rs1392172199 Functional Loss SNV dbSNP153 33..33 33 - - - 107999 RMVar_ID_107999 Human_SNP_ID_679354213 m1A Human chr20 - 33656485 33656485 33656485 CTGAGGAGAAGGAGGGCTTGCCTGGTTGAACCAAGGGTGACCCAGTAGCGGGGCTGAGCTGGGGG CTGAGGAGAAGGAGGGCTTGCCTGGTTGAACCGAGGGTGACCCAGTAGCGGGGCTGAGCTGGGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33656385..33656626 26863196 MeRIP-seq:(Medium) rs777566771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14072396 108000 RMVar_ID_108000 Human_SNP_ID_679354480 m1A Human chr20 + 33657441 33657441 33657441 AGCCCTGCTTCTGCCGCTGGCTGAGGAGGAGCAGAAGCCTGGTCCCAAGACAGCAGGAAGAAAGC AGCCCTGCTTCTGCCGCTGGCTGAGGAGGAGCGGAAGCCTGGTCCCAAGACAGCAGGAAGAAAGC A G L13712-001,lnc-C20orf144-1 RNACentral:URS0000334622,RNACentral:URS00001F704B misc_RNA,lincRNA intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33657136..33657736 32194978 MeRIP-seq:(Medium) rs1304221115 Functional Loss SNV dbSNP153 33..33 33 - - - 108001 RMVar_ID_108001 Human_SNP_ID_679354593 m1A Human chr20 - 33657809 33657809 33657809 GAATAACAACTGAGCCAGACCTGCACACGCCGAGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGA GAATAACAACTGAGCCAGACCTGCACACGCCGTGGGCCCCGGGACCCTGCCTGCCTCCCTCTGGA T A NECAB3 Ensembl:ENSG00000125967 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33657763..33658018 26863196 MeRIP-seq:(Medium) rs375312800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119149,Human_RBP_ID_9388965,Human_RBP_ID_19005368,Human_RBP_ID_27484618 Human_Splice_Rec_2073158,Human_Splice_Rec_2073180,Human_Splice_Rec_2073204,Human_Splice_Rec_2073220,Human_Splice_Rec_2073242,Human_Splice_Rec_2073256,Human_Splice_Rec_2073280,Human_Splice_Rec_2073296,Human_Splice_Rec_2073312,Human_Splice_Rec_2073328 Human_miRNA_ID_2018101,Human_miRNA_ID_2018102,Human_miRNA_ID_2691190,Human_miRNA_ID_2691191 RMVar_hsa_circ_87979,RMVar_hsa_circ_110565,RMVar_hsa_circ_121978,RMVar_hsa_circ_96806,RMVar_hsa_circ_209429,RMVar_hsa_circ_209430,RMVar_hsa_circ_209431,RMVar_hsa_circ_209428 108002 RMVar_ID_108002 Human_SNP_ID_679354977 m1A Human chr20 - 33658860 33658860 33658860 GCCAGTCCCTCCCCTGTGCCCGGCCCCGCACCAGCTGACCGGCTGCCTCTCCCACCAGCACATCC GCCAGTCCCTCCCCTGTGCCCGGCCCCGCACCGGCTGACCGGCTGCCTCTCCCACCAGCACATCC T C NECAB3 Ensembl:ENSG00000125967 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33658858..33658926 26863196 MeRIP-seq:(Medium) rs755511079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244435,Human_RBP_ID_22417570,Human_RBP_ID_22549093,Human_RBP_ID_22670786 RMVar_hsa_circ_87979,RMVar_hsa_circ_110565,RMVar_hsa_circ_121978,RMVar_hsa_circ_96806,RMVar_hsa_circ_209429,RMVar_hsa_circ_209430,RMVar_hsa_circ_209431,RMVar_hsa_circ_209428 108003 RMVar_ID_108003 Human_SNP_ID_679355054 m1A Human chr20 - 33659168 33659166 33659168 ACCCTTGGAGACAGGGAGAAGAGGATGGAGACAGGGAGGCTGGGGGGCAGGTTGGCGGCAGGAAC ACCCTTGGAGACAGGGAGAAGAGGATGGAGAC__GGAGGCTGGGGGGCAGGTTGGCGGCAGGAAC CCT C NECAB3 Ensembl:ENSG00000125967 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33659123..33659250 26863196 MeRIP-seq:(Medium) rs1474043218 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1068144,Human_RBP_ID_9347995,Human_RBP_ID_9431259,Human_RBP_ID_18950447,Human_RBP_ID_19106213,Human_RBP_ID_26342805 RMVar_hsa_circ_87979,RMVar_hsa_circ_110565,RMVar_hsa_circ_121978,RMVar_hsa_circ_96806,RMVar_hsa_circ_209429,RMVar_hsa_circ_209430,RMVar_hsa_circ_209431,RMVar_hsa_circ_209428 108004 RMVar_ID_108004 Human_SNP_ID_679355055 m1A Human chr20 - 33659168 33659168 33659168 ACCCTTGGAGACAGGGAGAAGAGGATGGAGACAGGGAGGCTGGGGGGCAGGTTGGCGGCAGGAAC ACCCTTGGAGACAGGGAGAAGAGGATGGAGACTGGGAGGCTGGGGGGCAGGTTGGCGGCAGGAAC T A NECAB3 Ensembl:ENSG00000125967 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33659123..33659250 26863196 MeRIP-seq:(Medium) rs1362528646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1068144,Human_RBP_ID_9347995,Human_RBP_ID_9431259,Human_RBP_ID_18950447,Human_RBP_ID_19106213,Human_RBP_ID_26342805 RMVar_hsa_circ_87979,RMVar_hsa_circ_110565,RMVar_hsa_circ_121978,RMVar_hsa_circ_96806,RMVar_hsa_circ_209429,RMVar_hsa_circ_209430,RMVar_hsa_circ_209431,RMVar_hsa_circ_209428 108005 RMVar_ID_108005 Human_SNP_ID_679356560 m1A Human chr20 + 33663674 33663674 33663674 ATTGCGCGGAGCGGGCGAAGGTAGCGAGCGCGAGCCGAGGATGCCGGTACTGCTGCTGCTGCGGC ATTGCGCGGAGCGGGCGAAGGTAGCGAGCGCGGGCCGAGGATGCCGGTACTGCTGCTGCTGCGGC A G C20orf144 Ensembl:ENSG00000149609 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:33663463..33663709 26863410 MeRIP-seq:(Medium) rs1441607763 Functional Loss SNV dbSNP153 33..33 33 - - - 108006 RMVar_ID_108006 Human_SNP_ID_679356917 m1A Human chr20 + 33664669 33664669 33664669 CACTCCCCAAATCACTTAGAAGAAGCCCTGCCACACTTTCTGTGGGCGGGATCCTGCTGCTGCTT CACTCCCCAAATCACTTAGAAGAAGCCCTGCCTCACTTTCTGTGGGCGGGATCCTGCTGCTGCTT A T C20orf144 Ensembl:ENSG00000149609 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33664665..33664797 26863196 MeRIP-seq:(Medium) rs1181902974 Functional Loss SNV dbSNP153 33..33 33 - - - 108007 RMVar_ID_108007 Human_SNP_ID_679359739 m1A Human chr20 + 33674222 33674222 33674222 GGAGACACCGCGAGCAGAGCCCGCGCCCACTCACGTCCTGGAAGAGCGTGTGTCCGGCGGGCCCC GGAGACACCGCGAGCAGAGCCCGCGCCCACTCCCGTCCTGGAAGAGCGTGTGTCCGGCGGGCCCC A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33674220..33674376 26863196 MeRIP-seq:(Medium) rs767746127 Functional Loss SNV dbSNP153 33..33 33 - - - 108008 RMVar_ID_108008 Human_SNP_ID_679359781 m1A Human chr20 - 33674331 33674331 33674331 GTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCACCGTGTGCCTGCTCCGGCCGCCCGCGCCCCAG GTGGCGGCGCCATGGCGTGCGCGGGGCTGCTCGCCGTGTGCCTGCTCCGGCCGCCCGCGCCCCAG T C NECAB3 Ensembl:ENSG00000125967 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:33674251..33674400 26863410 MeRIP-seq:(Medium) rs868543717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4642092,Human_RBP_ID_18422857 RMVar_hsa_circ_87979,RMVar_hsa_circ_209431 108009 RMVar_ID_108009 Human_SNP_ID_679359799 m1A Human chr20 + 33674362 33674362 33674362 GTGAGCAGCCCCGCGCACGCCATGGCGCCGCCACCCGCTCGGGCTCGGCTGCGGTTGCTGCCGAC GTGAGCAGCCCCGCGCACGCCATGGCGCCGCCGCCCGCTCGGGCTCGGCTGCGGTTGCTGCCGAC A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33674209..33674378 26863196 MeRIP-seq:(Medium) rs1193228382 Functional Loss SNV dbSNP153 33..33 33 - - - 108010 RMVar_ID_108010 Human_SNP_ID_679360264 m1A Human chr20 + 33675941 33675941 33675941 GGCAGCTGGGGCCCTGAACTGGCCCCCTGGAGAGGGCCCACCCCACCATCTGACCACCCATGGCT GGCAGCTGGGGCCCTGAACTGGCCCCCTGGAGCGGGCCCACCCCACCATCTGACCACCCATGGCT A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33675894..33675984 26863196 MeRIP-seq:(Medium) rs1404302955 Functional Loss SNV dbSNP153 33..33 33 - - - 108011 RMVar_ID_108011 Human_SNP_ID_679360335 m1A Human chr20 - 33676223 33676223 33676223 AGGCTTTGGCTGGCTGGGCGTGTAGGACGGTGAGAGCACTTCTGTCTTAAAGGTTTTTTCTGATT AGGCTTTGGCTGGCTGGGCGTGTAGGACGGTGGGAGCACTTCTGTCTTAAAGGTTTTTTCTGATT T C E2F1 Ensembl:ENSG00000101412 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33676174..33676265 26863196 MeRIP-seq:(Medium) rs968170858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_561837,Human_RBP_ID_779823,Human_RBP_ID_1595122,Human_RBP_ID_6991324,Human_RBP_ID_8530871,Human_RBP_ID_8853759,Human_RBP_ID_14072592,Human_RBP_ID_17142296,Human_RBP_ID_17969866,Human_RBP_ID_18321654,Human_RBP_ID_18770987,Human_RBP_ID_23900484,Human_RBP_ID_27700994 108012 RMVar_ID_108012 Human_SNP_ID_679360712 m1A Human chr20 + 33677160 33677160 33677160 TGGCTGGGATCTGTGGTGAGGGATGAGGGGGGAGATGATGGTGGTGGTGACACTATGGTGGCAGA TGGCTGGGATCTGTGGTGAGGGATGAGGGGGGGGATGATGGTGGTGGTGACACTATGGTGGCAGA A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33677098..33677242 26863196 MeRIP-seq:(Medium) rs111268294 Functional Loss SNV dbSNP153 33..33 33 - - - 108013 RMVar_ID_108013 Human_SNP_ID_679360713 m1A Human chr20 + 33677160 33677160 33677160 TGGCTGGGATCTGTGGTGAGGGATGAGGGGGGAGATGATGGTGGTGGTGACACTATGGTGGCAGA TGGCTGGGATCTGTGGTGAGGGATGAGGGGGGTGATGATGGTGGTGGTGACACTATGGTGGCAGA A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33677098..33677242 26863196 MeRIP-seq:(Medium) rs111268294 Functional Loss SNV dbSNP153 33..33 33 - - - 108014 RMVar_ID_108014 Human_SNP_ID_679369615 m1A Human chr20 - 33709948 33709947 33709948 CGTGGTTCTGTATAGAGGTAGGAGTGGGAGAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGTGGGG CGTGGTTCTGTATAGAGGTAGGAGTGGGAGAA_GGGCGTGGTTCAGTGTAGAGTTAGGAGTGGGG CT C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33709943..33710107 26863196 MeRIP-seq:(Medium) rs1260805739 Functional Loss DEL dbSNP153 33..33 33 - - - 108015 RMVar_ID_108015 Human_SNP_ID_679369616 m1A Human chr20 - 33709948 33709948 33709948 CGTGGTTCTGTATAGAGGTAGGAGTGGGAGAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGTGGGG CGTGGTTCTGTATAGAGGTAGGAGTGGGAGAAGGGGCGTGGTTCAGTGTAGAGTTAGGAGTGGGG T C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33709943..33710107 26863196 MeRIP-seq:(Medium) rs1159491837 Functional Loss SNV dbSNP153 33..33 33 - - - 108016 RMVar_ID_108016 Human_SNP_ID_679369617 m1A Human chr20 - 33709952 33709951 33709952 AGGGCGTGGTTCTGTATAGAGGTAGGAGTGGGAGAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGT AGGGCGTGGTTCTGTATAGAGGTAGGAGTGGG_GAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGT CT C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33709915..33710129 26863196 MeRIP-seq:(Medium) rs1322433528 Functional Loss DEL dbSNP153 33..33 33 - - - 108017 RMVar_ID_108017 Human_SNP_ID_679369618 m1A Human chr20 - 33709952 33709952 33709952 AGGGCGTGGTTCTGTATAGAGGTAGGAGTGGGAGAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGT AGGGCGTGGTTCTGTATAGAGGTAGGAGTGGGGGAAAGGGCGTGGTTCAGTGTAGAGTTAGGAGT T C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33709915..33710129 26863196 MeRIP-seq:(Medium) rs1203665384 Functional Loss SNV dbSNP153 33..33 33 - - - 108018 RMVar_ID_108018 Human_SNP_ID_679370459 m1A Human chr20 - 33713260 33713260 33713260 AGGATCCTGCTTGATAAGTGTGAGGAGGCTGGAGCAGAGGGGCTGAAGGGGAGAGAGGACAGAGA AGGATCCTGCTTGATAAGTGTGAGGAGGCTGGGGCAGAGGGGCTGAAGGGGAGAGAGGACAGAGA T C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33713259..33713463 26863196 MeRIP-seq:(Medium) rs1480779540 Functional Loss SNV dbSNP153 33..33 33 - - - 108019 RMVar_ID_108019 Human_SNP_ID_679372219 m1A Human chr20 - 33720228 33720228 33720228 GGCTGTCAGTGCGCTTACAGTTCCTAACCCCGACCCTGCGCGCAGCCCGCACTATGGCAGCCCCG GGCTGTCAGTGCGCTTACAGTTCCTAACCCCGCCCCTGCGCGCAGCCCGCACTATGGCAGCCCCG T G PXMP4 Ensembl:ENSG00000101417 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33720180..33720249 26863196 MeRIP-seq:(Medium) rs990501503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659740,Human_RBP_ID_5445523,Human_RBP_ID_18444210 108020 RMVar_ID_108020 Human_SNP_ID_679375272 m1A Human chr20 - 33732406 33732406 33732406 CCGCACCCCCGTCCCGGGCCCCGCGCGCCGCCAAGCCGCCTCCCTGGCCGCGGCTGTTCCAGACC CCGCACCCCCGTCCCGGGCCCCGCGCGCCGCCTAGCCGCCTCCCTGGCCGCGGCTGTTCCAGACC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33732216..33732493 26863196 MeRIP-seq:(Medium) rs542641145 Functional Loss SNV dbSNP153 33..33 33 - - - 108021 RMVar_ID_108021 Human_SNP_ID_679375273 m1A Human chr20 - 33732406 33732406 33732406 CCGCACCCCCGTCCCGGGCCCCGCGCGCCGCCAAGCCGCCTCCCTGGCCGCGGCTGTTCCAGACC CCGCACCCCCGTCCCGGGCCCCGCGCGCCGCCGAGCCGCCTCCCTGGCCGCGGCTGTTCCAGACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:33732216..33732493 26863196 MeRIP-seq:(Medium) rs542641145 Functional Loss SNV dbSNP153 33..33 33 - - - 108022 RMVar_ID_108022 Human_SNP_ID_679394407 m1A Human chr20 + 33811379 33811379 33811379 AGGAGAGGCCTGCGGCGGCAGGGAGCGGCGGGACTGGGAGCGGGCGCCGGAGCCGACCCGAGCCG AGGAGAGGCCTGCGGCGGCAGGGAGCGGCGGGGCTGGGAGCGGGCGCCGGAGCCGACCCGAGCCG A G CHMP4B Ensembl:ENSG00000101421 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:33811301..33811500 26863196 MeRIP-seq:(Medium) rs937272741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659336,Human_RBP_ID_9331484,Human_RBP_ID_9388981,Human_RBP_ID_18423072,Human_RBP_ID_22533616,Human_RBP_ID_23004848,Human_RBP_ID_24379947,Human_RBP_ID_26342807,Human_RBP_ID_27819637 RMVar_hsa_circ_93031,RMVar_hsa_circ_209452 108023 RMVar_ID_108023 Human_SNP_ID_679394409 m1A Human chr20 - 33811381 33811381 33811381 CTCGGCTCGGGTCGGCTCCGGCGCCCGCTCCCAGTCCCGCCGCTCCCTGCCGCCGCAGGCCTCTC CTCGGCTCGGGTCGGCTCCGGCGCCCGCTCCCGGTCCCGCCGCTCCCTGCCGCCGCAGGCCTCTC T C ZNF341-AS1,ZNF341-AS1:2,ZNF341-AS1:3,ZNF341-AS1:4 RNACentral:URS0000D57835,RNACentral:URS0000D5D84C,RNACentral:URS0000D5C7B1,RNACentral:URS0000D58E2A lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:33811273..33811692;chr20:33811251..33848511 26863196 MeRIP-seq:(Medium) rs1221627680 Functional Loss SNV dbSNP153 33..33 33 - - - 108024 RMVar_ID_108024 Human_SNP_ID_679394441 m1A Human chr20 + 33811445 33811445 33811445 GCCGAGCCGAGCCGAGCCGGAGCGGGCGGCGAAGGCCGGCGCGGCGAGCAGCAACCATGTCGGTG GCCGAGCCGAGCCGAGCCGGAGCGGGCGGCGAGGGCCGGCGCGGCGAGCAGCAACCATGTCGGTG A G CHMP4B Ensembl:ENSG00000101421 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:33811346..33811446 26863410 MeRIP-seq:(Medium) rs558991361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244315,Human_RBP_ID_4642264,Human_RBP_ID_18423072,Human_RBP_ID_19106233,Human_RBP_ID_26343497,Human_RBP_ID_27158884 RMVar_hsa_circ_93031,RMVar_hsa_circ_209452 108025 RMVar_ID_108025 Human_SNP_ID_679394451 m1A Human chr20 + 33811465 33811465 33811465 AGCGGGCGGCGAAGGCCGGCGCGGCGAGCAGCAACCATGTCGGTGTTCGGGAAGCTGTTCGGGGC AGCGGGCGGCGAAGGCCGGCGCGGCGAGCAGCGACCATGTCGGTGTTCGGGAAGCTGTTCGGGGC A G CHMP4B Ensembl:ENSG00000101421 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:33811251..33811685 26863196 MeRIP-seq:(Medium) rs768152066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1928060,Human_RBP_ID_4659336,Human_RBP_ID_18771032 RMVar_hsa_circ_93031,RMVar_hsa_circ_209452 108026 RMVar_ID_108026 Human_SNP_ID_679394505 m1A Human chr20 + 33811607 33811607 33811607 TAAGCAAGAAACAGGAGTTCCTGGAGAAGAAAATCGAGCAGGAGCTGACGGCCGCCAAGAAGCAC TAAGCAAGAAACAGGAGTTCCTGGAGAAGAAAGTCGAGCAGGAGCTGACGGCCGCCAAGAAGCAC A G CHMP4B Ensembl:ENSG00000101421 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33811403..33853668 32194978 MeRIP-seq:(Medium) rs1361445390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62527,Human_RBP_ID_9116323,Human_RBP_ID_9388983,Human_RBP_ID_17969913 Human_Splice_Rec_2073611 RMVar_hsa_circ_93031,RMVar_hsa_circ_209452 108027 RMVar_ID_108027 Human_SNP_ID_679402478 m1A Human chr20 + 33848601 33848601 33848601 ATGCCAACACCAACACCGAGGTGCTCAAGAACATGGGCTATGCCGCCAAGGCCATGAAGGCGGCC ATGCCAACACCAACACCGAGGTGCTCAAGAACTTGGGCTATGCCGCCAAGGCCATGAAGGCGGCC A T CHMP4B Ensembl:ENSG00000101421 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33848551..33848600 26863196 MeRIP-seq:(Medium) rs1222300544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62528,Human_RBP_ID_1928063,Human_RBP_ID_18444214,Human_RBP_ID_27819638 Human_Splice_Rec_2073613 RMVar_hsa_circ_16427,RMVar_hsa_circ_93031,RMVar_hsa_circ_118507,RMVar_hsa_circ_209452,RMVar_hsa_circ_209453 108028 RMVar_ID_108028 Human_SNP_ID_679403554 m1A Human chr20 + 33853551 33853551 33853551 GACGACATGAAGGAATTGGAGAACTGGGCTGGATCCATGTAATGGGGTCCAGCGCTGGCTGGGCC GACGACATGAAGGAATTGGAGAACTGGGCTGGTTCCATGTAATGGGGTCCAGCGCTGGCTGGGCC A T CHMP4B Ensembl:ENSG00000101421 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:33853501..33853750;chr20:33853526..33853550 26863196 MeRIP-seq:(Medium) rs1175086822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62532,Human_RBP_ID_561902,Human_RBP_ID_924440,Human_RBP_ID_1025490,Human_RBP_ID_1135732,Human_RBP_ID_1601117,Human_RBP_ID_5119150,Human_RBP_ID_5147879,Human_RBP_ID_5200614,Human_RBP_ID_6991544,Human_RBP_ID_9388987,Human_RBP_ID_17659013,Human_RBP_ID_17700309,Human_RBP_ID_18412852,Human_RBP_ID_19004009,Human_RBP_ID_23004755,Human_RBP_ID_23900611,Human_RBP_ID_26342412,Human_RBP_ID_27019594,Human_RBP_ID_27820158 Human_Splice_Rec_2073618 Human_miRNA_ID_2899350,Human_miRNA_ID_2975158,Human_miRNA_ID_3008353,Human_miRNA_ID_3096237 RMVar_hsa_circ_81174,RMVar_hsa_circ_93031,RMVar_hsa_circ_118507,RMVar_hsa_circ_209452,RMVar_hsa_circ_83494,RMVar_hsa_circ_209453,RMVar_hsa_circ_84690,RMVar_hsa_circ_209454,RMVar_hsa_circ_209455,RMVar_hsa_circ_209456 108029 RMVar_ID_108029 Human_SNP_ID_679439401 m1A Human chr20 + 33998600 33998600 33998600 CAGACAGGAGACTTTCAAGGTAGGCAGAGCAGAGGCCAAGTCAGGAAAGGGCCTTCTTGCCTGTG CAGACAGGAGACTTTCAAGGTAGGCAGAGCAGTGGCCAAGTCAGGAAAGGGCCTTCTTGCCTGTG A T RALY Ensembl:ENSG00000125970 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:33998595..33998727 26863196 MeRIP-seq:(Medium) rs1213677015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17193043 108030 RMVar_ID_108030 Human_SNP_ID_679458651 m1A Human chr20 - 34075955 34075955 34075955 ACAGGTACGTTAGTTTTGACACGCCGGACCAAAGGGACTGTGACCCGGGGTCGCTTCACAGGGAC ACAGGTACGTTAGTTTTGACACGCCGGACCAATGGGACTGTGACCCGGGGTCGCTTCACAGGGAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:34073562..34076025 32194978 MeRIP-seq:(Medium) rs759168900 Functional Loss SNV dbSNP153 33..33 33 - - - 108031 RMVar_ID_108031 Human_SNP_ID_679458672 m1A Human chr20 - 34075997 34075997 34075997 GCTGAGCTGGTGGTGACAGCTGTGGAGCGGGCAAAGAGCTTGACAGGTACGTTAGTTTTGACACG GCTGAGCTGGTGGTGACAGCTGTGGAGCGGGCGAAGAGCTTGACAGGTACGTTAGTTTTGACACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34075840..34076071 26863196 MeRIP-seq:(Medium) rs760014031 Functional Loss SNV dbSNP153 33..33 33 - - - 108032 RMVar_ID_108032 Human_SNP_ID_679459045 m1A Human chr20 - 34077095 34077071 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCC________________________GCCGCCGCC CGGTGGTGGTGGCAGCGGTGGCGGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs1225689816 Functional Loss DEL dbSNP153 33..56 33 - - - 108033 RMVar_ID_108033 Human_SNP_ID_679459073 m1A Human chr20 - 34077095 34077086 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCC_________GCTGCCACCACCACCGCCGCCGCC CGGTGGCGGT C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs749336492 Functional Loss DEL dbSNP153 33..41 33 - - - 108034 RMVar_ID_108034 Human_SNP_ID_679459086 m1A Human chr20 - 34077095 34077095 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCCTCCGCCACCGCTGCCACCACCACCGCCGCCGCC T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs781060935 Functional Loss SNV dbSNP153 33..33 33 - - - 108035 RMVar_ID_108035 Human_SNP_ID_679459087 m1A Human chr20 - 34077095 34077095 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCCGCCGCCACCGCTGCCACCACCACCGCCGCCGCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs781060935 Functional Loss SNV dbSNP153 33..33 33 - - - 108036 RMVar_ID_108036 Human_SNP_ID_679459088 m1A Human chr20 - 34077095 34077095 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCCCCCGCCACCGCTGCCACCACCACCGCCGCCGCC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs781060935 Functional Loss SNV dbSNP153 33..33 33 - - - 108037 RMVar_ID_108037 Human_SNP_ID_679459493 m1A Human chr20 + 34078456 34078455 34078457 TTTTTCTGGACAAATGGCTCAGGGCAGGACTCAGAGCTGGCAATGAGTGATGTGTGGTCTCTCTT TTTTTCTGGACAAATGGCTCAGGGCAGGACTC__AGCTGGCAATGAGTGATGTGTGGTCTCTCTT CAG C RALY Ensembl:ENSG00000125970 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34078454..34078599 26863196 MeRIP-seq:(Medium) rs1271585986 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5383596,Human_RBP_ID_6991781,Human_RBP_ID_8530975,Human_RBP_ID_22671384 Human_Splice_Rec_2073651,Human_Splice_Rec_2073689,Human_Splice_Rec_2073731 RMVar_hsa_circ_322233,RMVar_hsa_circ_209466,RMVar_hsa_circ_209460,RMVar_hsa_circ_271396,RMVar_hsa_circ_266613,RMVar_hsa_circ_49386,RMVar_hsa_circ_209471,RMVar_hsa_circ_209472 108038 RMVar_ID_108038 Human_SNP_ID_679459838 m1A Human chr20 - 34079861 34079861 34079861 GAGAAAGAAGAGACTAAGGCTGAGAGGAAGAGACCCTGTTGCTGATAAAAGGGGTAGGGAAGAAA GAGAAAGAAGAGACTAAGGCTGAGAGGAAGAGTCCCTGTTGCTGATAAAAGGGGTAGGGAAGAAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:34079859..34080086 26863196 MeRIP-seq:(Medium) rs535990206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14074275 108039 RMVar_ID_108039 Human_SNP_ID_679459839 m1A Human chr20 - 34079863 34079863 34079863 GAGAGAAAGAAGAGACTAAGGCTGAGAGGAAGAGACCCTGTTGCTGATAAAAGGGGTAGGGAAGA GAGAGAAAGAAGAGACTAAGGCTGAGAGGAAGGGACCCTGTTGCTGATAAAAGGGGTAGGGAAGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34079860..34080106 26863196 MeRIP-seq:(Medium) rs1445229017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14074275 108040 RMVar_ID_108040 Human_SNP_ID_679459886 m1A Human chr20 + 34080024 34080024 34080024 CCCCCAGCGGGTACCAGAGGAAAGCTGGCAGCAGGCGCCTCCTCCCCCAACGCATCCCAGCCAGT CCCCCAGCGGGTACCAGAGGAAAGCTGGCAGCGGGCGCCTCCTCCCCCAACGCATCCCAGCCAGT A G RALY Ensembl:ENSG00000125970 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34079860..34080171 26863196 MeRIP-seq:(Medium) rs893387677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_561955,Human_RBP_ID_5118915,Human_RBP_ID_6991786,Human_RBP_ID_17659016,Human_RBP_ID_22453023 Human_miRNA_ID_1094440 RMVar_hsa_circ_266613,RMVar_hsa_circ_209472 108041 RMVar_ID_108041 Human_SNP_ID_679466198 m1A Human chr20 - 34105451 34105451 34105451 TGAGGAAGGGGATACCCAAACAGAGGAAACCCAGCCTTCAGAAACAAAAGAAGTGGAGCCAGAGC TGAGGAAGGGGATACCCAAACAGAGGAAACCCGGCCTTCAGAAACAAAAGAAGTGGAGCCAGAGC T C EIF2S2 Ensembl:ENSG00000125977 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:34103487..34105450 32194978 MeRIP-seq:(Medium) rs1483428965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244858,Human_RBP_ID_1595295,Human_RBP_ID_2681784,Human_RBP_ID_8234963,Human_RBP_ID_9389018,Human_RBP_ID_22817172,Human_RBP_ID_24546649,Human_RBP_ID_26342826,Human_RBP_ID_26489635,Human_RBP_ID_27019642,Human_RBP_ID_27819653 Human_Splice_Rec_2073738,Human_Splice_Rec_2073739 RMVar_hsa_circ_4267,RMVar_hsa_circ_19288,RMVar_hsa_circ_59414,RMVar_hsa_circ_363726,RMVar_hsa_circ_369076 108042 RMVar_ID_108042 Human_SNP_ID_679467702 m1A Human chr20 - 34111850 34111850 34111850 CTCCTGCCGTGGTTGGCGTTTCCGGAATGGAGAGCACACGTTGAGTCGTCCTCCCGGAAGGGGCT CTCCTGCCGTGGTTGGCGTTTCCGGAATGGAGTGCACACGTTGAGTCGTCCTCCCGGAAGGGGCT T A EIF2S2 Ensembl:ENSG00000125977 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:34111839..34111943 26863196 MeRIP-seq:(Medium) rs1309493537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1595303 108043 RMVar_ID_108043 Human_SNP_ID_679467803 m1A Human chr20 + 34112144 34112143 34112144 GCTGCGGCTCGAGTGGGCTCGGCACGGACGGGAAGTCAGACGGGTCAGCCCCAGGCCCCGGCGGC GCTGCGGCTCGAGTGGGCTCGGCACGGACGGG_AGTCAGACGGGTCAGCCCCAGGCCCCGGCGGC GA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:34105451..34112250;chr20:34112134..34112234 26863410 MeRIP-seq:(Medium) rs1568722255 Functional Loss DEL dbSNP153 33..33 33 - - - 108044 RMVar_ID_108044 Human_SNP_ID_679508445 m1A Human chr20 - 34281008 34281002 34281009 CTACTGAGAGCCAGGTCTGCGTTTCACCCTCCAGCTGCTGTCCTTGCCCAGGCCCCACCTCTCCT CTACTGAGAGCCAGGTCTGCGTTTCACCCTC_______TGTCCTTGCCCAGGCCCCACCTCTCCT AGCAGCTG A AHCY,AL035458.2 Ensembl:ENSG00000101444,Ensembl:ENSG00000250917 Protein coding,lincRNA 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34280633..34281113 26863196 MeRIP-seq:(Medium) rs760263204 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_63354,Human_RBP_ID_562101,Human_RBP_ID_779355,Human_RBP_ID_3657291,Human_RBP_ID_4642532,Human_RBP_ID_5100496,Human_RBP_ID_5119152,Human_RBP_ID_5147882,Human_RBP_ID_8260688,Human_RBP_ID_8531092,Human_RBP_ID_17659297,Human_RBP_ID_18193616,Human_RBP_ID_22506426,Human_RBP_ID_27019663,Human_RBP_ID_27488876 Human_miRNA_ID_173188 108045 RMVar_ID_108045 Human_SNP_ID_679510990 m1A Human chr20 + 34290864 34290864 34290864 CCATAGCCTGCTACCACCGCTACCTTGCCGGCAATCATCACATCTGTGGCCCGCTTGATGCCATC CCATAGCCTGCTACCACCGCTACCTTGCCGGCCATCATCACATCTGTGGCCCGCTTGATGCCATC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34290721..34290897 26863196 MeRIP-seq:(Medium) rs1432208351 Functional Loss SNV dbSNP153 33..33 33 - - - 108046 RMVar_ID_108046 Human_SNP_ID_679514316 m1A Human chr20 + 34303293 34303293 34303293 TGTCAGACATGCTGGCGGCACTCGTGATGGAAACGGGCGAAGGGGGCTGGGCCTCAGTCTGGGAA TGTCAGACATGCTGGCGGCACTCGTGATGGAAGCGGGCGAAGGGGGCTGGGCCTCAGTCTGGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:34303189..34303350;chr20:34303197..34303350 26863196 MeRIP-seq:(Medium) rs1406248189 Functional Loss SNV dbSNP153 33..33 33 - - - 108047 RMVar_ID_108047 Human_SNP_ID_679531080 m1A Human chr20 + 34370811 34370811 34370811 GAAGGAAGACTACTGGGTAAGAAAAAAAAAGTAGAACATAAAGTTAAGCAGTAAGAGAATAGGGA GAAGGAAGACTACTGGGTAAGAAAAAAAAAGTGGAACATAAAGTTAAGCAGTAAGAGAATAGGGA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34370761..34370860 26863196 MeRIP-seq:(Medium) rs985022647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14075740 RMVar_hsa_circ_278835,RMVar_hsa_circ_114271,RMVar_hsa_circ_332410,RMVar_hsa_circ_209504,RMVar_hsa_circ_287774,RMVar_hsa_circ_209506,RMVar_hsa_circ_209507,RMVar_hsa_circ_209505 108048 RMVar_ID_108048 Human_SNP_ID_679573195 m1A Human chr20 - 34534566 34534566 34534566 GATGTGGAGCCCCTTCTGCCGAGCTCCCACCCACACCCCTAATTGGGGAGAACTGGAATAGCAGT GATGTGGAGCCCCTTCTGCCGAGCTCCCACCCGCACCCCTAATTGGGGAGAACTGGAATAGCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34534563..34534750 26863196 MeRIP-seq:(Medium) rs917307776 Functional Loss SNV dbSNP153 33..33 33 - - - 108049 RMVar_ID_108049 Human_SNP_ID_679573234 m1A Human chr20 + 34534663 34534663 34534663 TTCCCATCAAGAGCACCATGGACAACCCCACCACCACCCAGTATGCCAGCCTCATGCACAGCTTC TTCCCATCAAGAGCACCATGGACAACCCCACCGCCACCCAGTATGCCAGCCTCATGCACAGCTTC A G ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:34534626..34534870 26863196 MeRIP-seq:(Medium) rs755467153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62834,Human_RBP_ID_927247,Human_RBP_ID_17283396,Human_RBP_ID_17396562,Human_RBP_ID_18534482,Human_RBP_ID_26342830,Human_RBP_ID_26821307,Human_RBP_ID_27019736,Human_RBP_ID_27488879,Human_RBP_ID_27564442 Human_Splice_Rec_2074102,Human_Splice_Rec_2074332,Human_Splice_Rec_2074340,Human_Splice_Rec_2074350 Human_miRNA_ID_3052529 RMVar_hsa_circ_1330,RMVar_hsa_circ_319692,RMVar_hsa_circ_333201,RMVar_hsa_circ_89108,RMVar_hsa_circ_112595,RMVar_hsa_circ_209558,RMVar_hsa_circ_209559 108050 RMVar_ID_108050 Human_SNP_ID_679573236 m1A Human chr20 + 34534678 34534666 34534679 CCATGGACAACCCCACCACCACCCAGTATGCCAGCCTCATGCACAGCTTCATCCTGAAGGCACGG CCATGGACAACCCCACCACCA_____________CCTCATGCACAGCTTCATCCTGAAGGCACGG ACCCAGTATGCCAG A ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34534571..34534832 26863196 MeRIP-seq:(Medium) rs1355228321 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_62834,Human_RBP_ID_17283396,Human_RBP_ID_17396562,Human_RBP_ID_18771261,Human_RBP_ID_22079076,Human_RBP_ID_22817188,Human_RBP_ID_26342830,Human_RBP_ID_26821307,Human_RBP_ID_27019736 Human_Splice_Rec_2074102,Human_Splice_Rec_2074332,Human_Splice_Rec_2074340,Human_Splice_Rec_2074350 Human_miRNA_ID_1396452,Human_miRNA_ID_2716544,Human_miRNA_ID_3052529 RMVar_hsa_circ_1330,RMVar_hsa_circ_319692,RMVar_hsa_circ_333201,RMVar_hsa_circ_89108,RMVar_hsa_circ_112595,RMVar_hsa_circ_209558,RMVar_hsa_circ_209559 108051 RMVar_ID_108051 Human_SNP_ID_679573241 m1A Human chr20 + 34534678 34534678 34534678 CCATGGACAACCCCACCACCACCCAGTATGCCAGCCTCATGCACAGCTTCATCCTGAAGGCACGG CCATGGACAACCCCACCACCACCCAGTATGCCGGCCTCATGCACAGCTTCATCCTGAAGGCACGG A G ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34534571..34534832 26863196 MeRIP-seq:(Medium) rs374598542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62834,Human_RBP_ID_17283396,Human_RBP_ID_17396562,Human_RBP_ID_18771261,Human_RBP_ID_22079076,Human_RBP_ID_22817188,Human_RBP_ID_26342830,Human_RBP_ID_26821307,Human_RBP_ID_27019736 Human_Splice_Rec_2074102,Human_Splice_Rec_2074332,Human_Splice_Rec_2074340,Human_Splice_Rec_2074350 Human_miRNA_ID_1396452,Human_miRNA_ID_2716544,Human_miRNA_ID_3052529 RMVar_hsa_circ_1330,RMVar_hsa_circ_319692,RMVar_hsa_circ_333201,RMVar_hsa_circ_89108,RMVar_hsa_circ_112595,RMVar_hsa_circ_209558,RMVar_hsa_circ_209559 108052 RMVar_ID_108052 Human_SNP_ID_679574691 m1A Human chr20 + 34540621 34540621 34540621 TATTTCCTGATTGTGATTCAGAATCCAACCGAATAAGCCACTCTCTTGGCTCCCTGTGTCATTCC TATTTCCTGATTGTGATTCAGAATCCAACCGAGTAAGCCACTCTCTTGGCTCCCTGTGTCATTCC A G ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:34540576..34540625 26863196 MeRIP-seq:(Medium) rs1218999670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562189,Human_RBP_ID_1379995,Human_RBP_ID_1595408,Human_RBP_ID_1928310,Human_RBP_ID_3646715,Human_RBP_ID_4642764,Human_RBP_ID_9331494,Human_RBP_ID_14077930,Human_RBP_ID_17281121,Human_RBP_ID_17395127,Human_RBP_ID_17511193,Human_RBP_ID_17659017,Human_RBP_ID_22453430,Human_RBP_ID_22670804,Human_RBP_ID_23901180,Human_RBP_ID_26489718 Human_Splice_Rec_2074104,Human_Splice_Rec_2074334,Human_Splice_Rec_2074342,Human_Splice_Rec_2074352 RMVar_hsa_circ_112595,RMVar_hsa_circ_209558 108053 RMVar_ID_108053 Human_SNP_ID_679574699 m1A Human chr20 - 34540639 34540639 34540639 TGGGGGGCATTAAATTAAGGAATGACACAGGGAGCCAAGAGAGTGGCTTATTCGGTTGGATTCTG TGGGGGGCATTAAATTAAGGAATGACACAGGGGGCCAAGAGAGTGGCTTATTCGGTTGGATTCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:34540601..34540650 26863196 MeRIP-seq:(Medium) rs1568605986 Functional Loss SNV dbSNP153 33..33 33 - - - 108054 RMVar_ID_108054 Human_SNP_ID_679574726 m1A Human chr20 + 34540732 34540732 34540732 ACTAGCACATGGCAGTCGCTTGGAACCCACTCACACCAATCCAGTGACCGTGTGTGGGCTGGCGG ACTAGCACATGGCAGTCGCTTGGAACCCACTCCCACCAATCCAGTGACCGTGTGTGGGCTGGCGG A C ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:34540681..34540768 26863196 MeRIP-seq:(Medium) rs542318079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562193,Human_RBP_ID_5148365,Human_RBP_ID_6993001,Human_RBP_ID_14077933,Human_RBP_ID_17281123,Human_RBP_ID_17395129,Human_RBP_ID_17512850,Human_RBP_ID_17659018,Human_RBP_ID_17970151,Human_RBP_ID_23901184,Human_RBP_ID_27484734,Human_RBP_ID_27564443 Human_miRNA_ID_2767750 RMVar_hsa_circ_112595,RMVar_hsa_circ_209558 108055 RMVar_ID_108055 Human_SNP_ID_679574748 m1A Human chr20 - 34540791 34540791 34540791 GCTCCGGAGCTCTGGGGAAGGTTGGTGCACACAGGGGTTCCGTTGGTGGGGGAGAAGAGCCGCCA GCTCCGGAGCTCTGGGGAAGGTTGGTGCACACGGGGGTTCCGTTGGTGGGGGAGAAGAGCCGCCA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:34540676..34540825 26863196 MeRIP-seq:(Medium) rs780005791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6993002 108056 RMVar_ID_108056 Human_SNP_ID_679574750 m1A Human chr20 - 34540795 34540795 34540795 GGGCGCTCCGGAGCTCTGGGGAAGGTTGGTGCACACAGGGGTTCCGTTGGTGGGGGAGAAGAGCC GGGCGCTCCGGAGCTCTGGGGAAGGTTGGTGCGCACAGGGGTTCCGTTGGTGGGGGAGAAGAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34540558..34540887 26863196 MeRIP-seq:(Medium) rs1032535966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6993002 108057 RMVar_ID_108057 Human_SNP_ID_679607472 m1A Human chr20 + 34677042 34677042 34677042 CGGCCAGACTGGAGCGGAACAAGGCCGCCCGCACTGTCACAGCCACCACCAGCACCAGGACCAAG CGGCCAGACTGGAGCGGAACAAGGCCGCCCGCCCTGTCACAGCCACCACCAGCACCAGGACCAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:34657228..34677080;chr20:34676921..34677058 26863196 MeRIP-seq:(Medium) rs1394037200 Functional Loss SNV dbSNP153 33..33 33 - - - 108058 RMVar_ID_108058 Human_SNP_ID_679615628 m1A Human chr20 - 34709372 34709372 34709372 TCCTCCAGGGGACTGCTCTGGAGGCGGGCGGGACCGAGTCCAGGCCCCTCTGCCGTAAAACAGGC TCCTCCAGGGGACTGCTCTGGAGGCGGGCGGGGCCGAGTCCAGGCCCCTCTGCCGTAAAACAGGC T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:34709327..34709479 26863196 MeRIP-seq:(Medium) rs757519019 Functional Loss SNV dbSNP153 33..33 33 - - - 108059 RMVar_ID_108059 Human_SNP_ID_679622958 m1A Human chr20 - 34741000 34741000 34741000 CAGCTTCCTTCCCCTCCTTGTACGTCTTCTCCAGTTGTCCCTTCTCATCCCCCTGTGCAGCAAGT CAGCTTCCTTCCCCTCCTTGTACGTCTTCTCCGGTTGTCCCTTCTCATCCCCCTGTGCAGCAAGT T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34740950..34741068 26863196 MeRIP-seq:(Medium) rs779855865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3646794,Human_RBP_ID_17085992,Human_RBP_ID_17512991,Human_RBP_ID_18950494 Human_miRNA_ID_2754931 RMVar_hsa_circ_22694,RMVar_hsa_circ_263,RMVar_hsa_circ_59999,RMVar_hsa_circ_366395,RMVar_hsa_circ_68416,RMVar_hsa_circ_344592,RMVar_hsa_circ_77727,RMVar_hsa_circ_209590 108060 RMVar_ID_108060 Human_SNP_ID_679625403 m1A Human chr20 - 34750386 34750386 34750386 AATCAGCAGGCTGGTACTTCTGGGGTTCCTCAAGTGAACCTCAGCAACATGCAAGGCCAGCCCCA AATCAGCAGGCTGGTACTTCTGGGGTTCCTCAGGTGAACCTCAGCAACATGCAAGGCCAGCCCCA T C NCOA6 Ensembl:ENSG00000198646 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs778314158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562283,Human_RBP_ID_1025580,Human_RBP_ID_9389035,Human_RBP_ID_17281150,Human_RBP_ID_17395153,Human_RBP_ID_17511224,Human_RBP_ID_18771340,Human_RBP_ID_27484776,Human_RBP_ID_27564450,Human_RBP_ID_27701161 RMVar_hsa_circ_22694,RMVar_hsa_circ_263,RMVar_hsa_circ_366395,RMVar_hsa_circ_72801,RMVar_hsa_circ_347024,RMVar_hsa_circ_344247 108061 RMVar_ID_108061 Human_SNP_ID_679627163 m1A Human chr20 - 34757727 34757727 34757727 CAGCCCAGGGTTCTCTGGGCACAATGACTGCAAACCAAGGGTGGAAGAAGGCTCCCTTGCCCGGC CAGCCCAGGGTTCTCTGGGCACAATGACTGCATACCAAGGGTGGAAGAAGGCTCCCTTGCCCGGC T A NCOA6 Ensembl:ENSG00000198646 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:34757678..34757810 26863196 MeRIP-seq:(Medium) rs779464895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18444243,Human_RBP_ID_27484785,Human_RBP_ID_27820179 RMVar_hsa_circ_2343,RMVar_hsa_circ_263,RMVar_hsa_circ_366395,RMVar_hsa_circ_72801,RMVar_hsa_circ_347024,RMVar_hsa_circ_12372,RMVar_hsa_circ_365118,RMVar_hsa_circ_349530,RMVar_hsa_circ_19863 108062 RMVar_ID_108062 Human_SNP_ID_679627164 m1A Human chr20 - 34757727 34757727 34757727 CAGCCCAGGGTTCTCTGGGCACAATGACTGCAAACCAAGGGTGGAAGAAGGCTCCCTTGCCCGGC CAGCCCAGGGTTCTCTGGGCACAATGACTGCAGACCAAGGGTGGAAGAAGGCTCCCTTGCCCGGC T C NCOA6 Ensembl:ENSG00000198646 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:34757678..34757810 26863196 MeRIP-seq:(Medium) rs779464895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18444243,Human_RBP_ID_27484785,Human_RBP_ID_27820179 RMVar_hsa_circ_2343,RMVar_hsa_circ_263,RMVar_hsa_circ_366395,RMVar_hsa_circ_72801,RMVar_hsa_circ_347024,RMVar_hsa_circ_12372,RMVar_hsa_circ_365118,RMVar_hsa_circ_349530,RMVar_hsa_circ_19863 108063 RMVar_ID_108063 Human_SNP_ID_679643036 m1A Human chr20 + 34825411 34825408 34825411 GGGCGGCGCCTCCTCCCCGCGAAGCCAGCCCGACAAGGACCGCGGACGCCCGGCGGGCCCACCCC GGGCGGCGCCTCCTCCCCGCGAAGCCAGCC___CAAGGACCGCGGACGCCCGGCGGGCCCACCCC CCGA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:34825407..34825650 26863196 MeRIP-seq:(Medium) rs933676757 Functional Loss DEL dbSNP153 31..33 33 - - - 108064 RMVar_ID_108064 Human_SNP_ID_679643061 m1A Human chr20 + 34825508 34825480 34825508 GCGCGGCCCCGGCCCTCCCGGGCGGGCCTTGGAGCGCCGGCCCGGGCCGTGCGTGCCCGCCGCCC GCGCG____________________________GCGCCGGCCCGGGCCGTGCGTGCCCGCCGCCC GGCCCCGGCCCTCCCGGGCGGGCCTTGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:34825325..34825620 26863196 MeRIP-seq:(Medium) rs1332042594 Functional Loss DEL dbSNP153 6..33 33 - - - 108065 RMVar_ID_108065 Human_SNP_ID_679643095 m1A Human chr20 - 34825569 34825569 34825569 GGCCGGGCGCGGGCGGCGGGACAGACGGGCGCACGCGAGGACTGACGGACGGACGCACCGAGGGC GGCCGGGCGCGGGCGGCGGGACAGACGGGCGCGCGCGAGGACTGACGGACGGACGCACCGAGGGC T C NCOA6 Ensembl:ENSG00000198646 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:34825377..34825654 26863196 MeRIP-seq:(Medium) rs1287781765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244962,Human_RBP_ID_4659349,Human_RBP_ID_9331843,Human_RBP_ID_9390381,Human_RBP_ID_9430752,Human_RBP_ID_17396568,Human_RBP_ID_18423316 Human_Splice_Rec_2074499,Human_Splice_Rec_2074527,Human_Splice_Rec_2074557 108066 RMVar_ID_108066 Human_SNP_ID_679654264 m1A Human chr20 - 34872769 34872769 34872769 CGAGGCCAGCCAGGAGAGCGCCCTGGGCGCCTACTCGCCAGTGGACTACATGAGCATCACCAGCT CGAGGCCAGCCAGGAGAGCGCCCTGGGCGCCTGCTCGCCAGTGGACTACATGAGCATCACCAGCT T C GGT7 Ensembl:ENSG00000131067 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34872718..34872810 26863196 MeRIP-seq:(Medium) rs774613710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422862,Human_RBP_ID_26342839 Human_miRNA_ID_2969829 RMVar_hsa_circ_100195,RMVar_hsa_circ_209610 108067 RMVar_ID_108067 Human_SNP_ID_679654279 m1A Human chr20 - 34872799 34872799 34872799 GGGGGCGCGGGCGAGGATGGCGGCGGAGAACGAGGCCAGCCAGGAGAGCGCCCTGGGCGCCTACT GGGGGCGCGGGCGAGGATGGCGGCGGAGAACGGGGCCAGCCAGGAGAGCGCCCTGGGCGCCTACT T C GGT7 Ensembl:ENSG00000131067 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:34872673..34872820 26863196 MeRIP-seq:(Medium) rs1320167514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18422862 RMVar_hsa_circ_100195,RMVar_hsa_circ_209610 108068 RMVar_ID_108068 Human_SNP_ID_679658066 m1A Human chr20 - 34888814 34888814 34888814 ACACCAGGCAGCAGCACATTTGTTCTCCACCTACCTGGAACATTTCCCCTCCCTACCCCAACTAT ACACCAGGCAGCAGCACATTTGTTCTCCACCTGCCTGGAACATTTCCCCTCCCTACCCCAACTAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:34888812..34888909 26863196 MeRIP-seq:(Medium) rs927531455 Functional Loss SNV dbSNP153 33..33 33 - - - 108069 RMVar_ID_108069 Human_SNP_ID_679667457 m1A Human chr20 + 34929545 34929545 34929545 GGATGTAGGAGGCCCTCTCCTCACTGTCCTTCAGCTGTTTCAGGGCCTGTACCATTTCCTCCCCA GGATGTAGGAGGCCCTCTCCTCACTGTCCTTCGGCTGTTTCAGGGCCTGTACCATTTCCTCCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:34929496..34931363 26863196 MeRIP-seq:(Medium) rs1231842587 Functional Loss SNV dbSNP153 33..33 33 - - - 108070 RMVar_ID_108070 Human_SNP_ID_679667458 m1A Human chr20 - 34929548 34929548 34929548 ATATGGGGAGGAAATGGTACAGGCCCTGAAACAGCTGAAGGACAGTGAGGAGAGGGCCTCCTACA ATATGGGGAGGAAATGGTACAGGCCCTGAAACGGCTGAAGGACAGTGAGGAGAGGGCCTCCTACA T C GSS Ensembl:ENSG00000100983 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34929498..34931363 26863196 MeRIP-seq:(Medium) rs774158841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562360,Human_RBP_ID_14080476 Human_Splice_Rec_2074914,Human_Splice_Rec_2074932,Human_Splice_Rec_2074952,Human_Splice_Rec_2074974,Human_Splice_Rec_2074992,Human_Splice_Rec_2075016,Human_Splice_Rec_2075040,Human_Splice_Rec_2075064,Human_Splice_Rec_2075082,Human_Splice_Rec_2075110,Human_Splice_Rec_2075130,Human_Splice_Rec_2075154,Human_Splice_Rec_2075170,Human_Splice_Rec_2075190,Human_Splice_Rec_2075192,Human_Splice_Rec_2075204 RMVar_hsa_circ_18563,RMVar_hsa_circ_90564,RMVar_hsa_circ_46704,RMVar_hsa_circ_209620 108071 RMVar_ID_108071 Human_SNP_ID_679668055 m1A Human chr20 + 34932077 34932077 34932077 TGCACCTTCTTAGTCCCAGCCAGCTGGGTGGCAATGTCTGGGCACTTGGCAGCATGTGACCTCTC TGCACCTTCTTAGTCCCAGCCAGCTGGGTGGCGATGTCTGGGCACTTGGCAGCATGTGACCTCTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:34932026..34932150 32194978 MeRIP-seq:(Medium) rs748978668 Functional Loss SNV dbSNP153 33..33 33 - - - 108072 RMVar_ID_108072 Human_SNP_ID_679672479 m1A Human chr20 - 34951846 34951846 34951846 TCTCTCCATCTTTTGCAGGTGTTGGGATGGCCACCAACTGGGGGAGCCTCTTGCAGGATAAACAG TCTCTCCATCTTTTGCAGGTGTTGGGATGGCCGCCAACTGGGGGAGCCTCTTGCAGGATAAACAG T C GSS Ensembl:ENSG00000100983 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:34951804..34951925 26863196 MeRIP-seq:(Medium) rs779292554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659762,Human_RBP_ID_5323220,Human_RBP_ID_5384983,Human_RBP_ID_9389042,Human_RBP_ID_17511233,Human_RBP_ID_23004954,Human_RBP_ID_26342844 Human_Splice_Rec_2074894,Human_Splice_Rec_2074918,Human_Splice_Rec_2074936,Human_Splice_Rec_2074956,Human_Splice_Rec_2074978,Human_Splice_Rec_2074996,Human_Splice_Rec_2075020,Human_Splice_Rec_2075044,Human_Splice_Rec_2075134,Human_Splice_Rec_2075174,Human_Splice_Rec_2075222,Human_Splice_Rec_2075238,Human_Splice_Rec_2075268,Human_Splice_Rec_2075276,Human_Splice_Rec_2075282,Human_Splice_Rec_2075290,Human_Splice_Rec_2075294,Human_Splice_Rec_2075298 RMVar_hsa_circ_46704,RMVar_hsa_circ_13141 108073 RMVar_ID_108073 Human_SNP_ID_679673410 m1A Human chr20 + 34955638 34955638 34955638 GGGTTTCAGCCACAAGGTCTCCCGGCCTCCGGAATTCCAATCTCTTGCCAGACCCCTCCCTCACA GGGTTTCAGCCACAAGGTCTCCCGGCCTCCGGCATTCCAATCTCTTGCCAGACCCCTCCCTCACA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:34955633..34955746 26863196 MeRIP-seq:(Medium) rs758263171 Functional Loss SNV dbSNP153 33..33 33 - - - 108074 RMVar_ID_108074 Human_SNP_ID_679673449 m1A Human chr20 + 34955747 34955747 34955747 GCCCCAACCTACTAGTTCGCCTTTCCTCCGCGAACGGTTCTCCCGGCCCTCGCGCCGCTACCCAG GCCCCAACCTACTAGTTCGCCTTTCCTCCGCGTACGGTTCTCCCGGCCCTCGCGCCGCTACCCAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34946074..34955800 26863196 MeRIP-seq:(Medium) rs886056641 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_697 108075 RMVar_ID_108075 Human_SNP_ID_679673452 m1A Human chr20 - 34955753 34955753 34955753 CTGAGCCTGGGTAGCGGCGCGAGGGCCGGGAGAACCGTTCGCGGAGGAAAGGCGAACTAGTAGGT CTGAGCCTGGGTAGCGGCGCGAGGGCCGGGAGTACCGTTCGCGGAGGAAAGGCGAACTAGTAGGT T A GSS Ensembl:ENSG00000100983 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34951681..34955800 26863196 MeRIP-seq:(Medium) rs942508014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659763,Human_RBP_ID_5118923 Human_Splice_Rec_2074893,Human_Splice_Rec_2074917,Human_Splice_Rec_2074935,Human_Splice_Rec_2074977,Human_Splice_Rec_2074995,Human_Splice_Rec_2075133,Human_Splice_Rec_2075173,Human_Splice_Rec_2075221,Human_Splice_Rec_2075275,Human_Splice_Rec_2075281,Human_Splice_Rec_2075289,Human_Splice_Rec_2075293,Human_Splice_Rec_2075295 108076 RMVar_ID_108076 Human_SNP_ID_679673460 m1A Human chr20 - 34955764 34955764 34955764 GGCCCCGCCCCCTGAGCCTGGGTAGCGGCGCGAGGGCCGGGAGAACCGTTCGCGGAGGAAAGGCG GGCCCCGCCCCCTGAGCCTGGGTAGCGGCGCGTGGGCCGGGAGAACCGTTCGCGGAGGAAAGGCG T A GSS Ensembl:ENSG00000100983 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34955647..34955800 26863196 MeRIP-seq:(Medium) rs886056642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4643118,Human_RBP_ID_5118923 Human_Splice_Rec_2074893,Human_Splice_Rec_2074917,Human_Splice_Rec_2074935,Human_Splice_Rec_2074977,Human_Splice_Rec_2074995,Human_Splice_Rec_2075133,Human_Splice_Rec_2075173,Human_Splice_Rec_2075221,Human_Splice_Rec_2075275,Human_Splice_Rec_2075281,Human_Splice_Rec_2075289,Human_Splice_Rec_2075293,Human_Splice_Rec_2075295 Clinvar_Rec_698,Clinvar_Rec_7192 108077 RMVar_ID_108077 Human_SNP_ID_679673461 m1A Human chr20 - 34955764 34955764 34955764 GGCCCCGCCCCCTGAGCCTGGGTAGCGGCGCGAGGGCCGGGAGAACCGTTCGCGGAGGAAAGGCG GGCCCCGCCCCCTGAGCCTGGGTAGCGGCGCGGGGGCCGGGAGAACCGTTCGCGGAGGAAAGGCG T C GSS Ensembl:ENSG00000100983 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34955647..34955800 26863196 MeRIP-seq:(Medium) rs886056642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4643118,Human_RBP_ID_5118923 Human_Splice_Rec_2074893,Human_Splice_Rec_2074917,Human_Splice_Rec_2074935,Human_Splice_Rec_2074977,Human_Splice_Rec_2074995,Human_Splice_Rec_2075133,Human_Splice_Rec_2075173,Human_Splice_Rec_2075221,Human_Splice_Rec_2075275,Human_Splice_Rec_2075281,Human_Splice_Rec_2075289,Human_Splice_Rec_2075293,Human_Splice_Rec_2075295 Clinvar_Rec_698,Clinvar_Rec_7192 108078 RMVar_ID_108078 Human_SNP_ID_679673470 m1A Human chr20 + 34955778 34955778 34955778 GAACGGTTCTCCCGGCCCTCGCGCCGCTACCCAGGCTCAGGGGGCGGGGCCTCGATGCGACCCAG GAACGGTTCTCCCGGCCCTCGCGCCGCTACCCGGGCTCAGGGGGCGGGGCCTCGATGCGACCCAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:34955634..34955800 26863196 MeRIP-seq:(Medium) rs1028995425 Functional Loss SNV dbSNP153 33..33 33 - - - 108079 RMVar_ID_108079 Human_SNP_ID_679687837 m1A Human chr20 - 35002781 35002781 35002781 CCAGAGTGGGGAGGAAGATATGGGTGACCCCCACCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC CCAGAGTGGGGAGGAAGATATGGGTGACCCCCTCCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC T A TRPC4AP Ensembl:ENSG00000100991 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5323221,Human_RBP_ID_8857485,Human_RBP_ID_17970310,Human_RBP_ID_23212290,Human_RBP_ID_26493018 Human_miRNA_ID_2691194 GWAS_ID_14852,GWAS_ID_14853,GWAS_ID_14854,GWAS_ID_14855,GWAS_ID_14856,GWAS_ID_14857,GWAS_ID_14858,GWAS_ID_14859,GWAS_ID_14860,GWAS_ID_14861,GWAS_ID_14862,GWAS_ID_14863,GWAS_ID_14864,GWAS_ID_14865,GWAS_ID_14866,GWAS_ID_14867,GWAS_ID_14868,GWAS_ID_14869,GWAS_ID_14870,GWAS_ID_14871,GWAS_ID_14872,GWAS_ID_14873,GWAS_ID_14874,GWAS_ID_14875,GWAS_ID_14876,GWAS_ID_14877,GWAS_ID_14878,GWAS_ID_14879,GWAS_ID_14880,GWAS_ID_14881,GWAS_ID_14882,GWAS_ID_14883,GWAS_ID_14884,GWAS_ID_14885,GWAS_ID_14886,GWAS_ID_14887,GWAS_ID_14888,GWAS_ID_14889,GWAS_ID_14890,GWAS_ID_14891,GWAS_ID_14892,GWAS_ID_14893,GWAS_ID_14894,GWAS_ID_14895,GWAS_ID_14896,GWAS_ID_14897,GWAS_ID_14898,GWAS_ID_14899,GWAS_ID_14900,GWAS_ID_14901,GWAS_ID_14902,GWAS_ID_14903,GWAS_ID_14904,GWAS_ID_14905,GWAS_ID_14906,GWAS_ID_14907,GWAS_ID_14908,GWAS_ID_14909,GWAS_ID_14910,GWAS_ID_14911,GWAS_ID_14912,GWAS_ID_14913,GWAS_ID_14914,GWAS_ID_14915,GWAS_ID_14916,GWAS_ID_14917,GWAS_ID_14918,GWAS_ID_14919,GWAS_ID_14920,GWAS_ID_14921,GWAS_ID_14922,GWAS_ID_14923,GWAS_ID_14924,GWAS_ID_14925,GWAS_ID_14926,GWAS_ID_14927,GWAS_ID_14928,GWAS_ID_14929,GWAS_ID_14930,GWAS_ID_14931,GWAS_ID_14932,GWAS_ID_14933,GWAS_ID_14934,GWAS_ID_14935,GWAS_ID_14936,GWAS_ID_14937,GWAS_ID_14938,GWAS_ID_14939,GWAS_ID_14940,GWAS_ID_14941,GWAS_ID_14942,GWAS_ID_14943,GWAS_ID_14944,GWAS_ID_14945,GWAS_ID_14946,GWAS_ID_14947,GWAS_ID_14948,GWAS_ID_14949,GWAS_ID_14950,GWAS_ID_14951,GWAS_ID_14952,GWAS_ID_14953,GWAS_ID_14954,GWAS_ID_14955,GWAS_ID_14956,GWAS_ID_14957,GWAS_ID_14958,GWAS_ID_14959,GWAS_ID_14960,GWAS_ID_14961,GWAS_ID_14962,GWAS_ID_14963,GWAS_ID_14964,GWAS_ID_14965,GWAS_ID_14966,GWAS_ID_14967,GWAS_ID_14968,GWAS_ID_14969,GWAS_ID_14970,GWAS_ID_14971,GWAS_ID_14972,GWAS_ID_14973,GWAS_ID_14974,GWAS_ID_14975,GWAS_ID_14976,GWAS_ID_14977,GWAS_ID_14978,GWAS_ID_14979,GWAS_ID_14980,GWAS_ID_14981,GWAS_ID_14982,GWAS_ID_14983,GWAS_ID_14984,GWAS_ID_14985,GWAS_ID_14986,GWAS_ID_14987,GWAS_ID_14988,GWAS_ID_14989,GWAS_ID_14990,GWAS_ID_14991,GWAS_ID_14992,GWAS_ID_14993,GWAS_ID_14994,GWAS_ID_14995,GWAS_ID_14996,GWAS_ID_14997,GWAS_ID_14998,GWAS_ID_14999,GWAS_ID_15000,GWAS_ID_15001,GWAS_ID_15002,GWAS_ID_15003,GWAS_ID_15004,GWAS_ID_15005,GWAS_ID_15006,GWAS_ID_15007,GWAS_ID_15008,GWAS_ID_15009,GWAS_ID_15010,GWAS_ID_15011,GWAS_ID_15012,GWAS_ID_15013,GWAS_ID_15014,GWAS_ID_15015,GWAS_ID_15016,GWAS_ID_15017,GWAS_ID_15018,GWAS_ID_15019,GWAS_ID_15020,GWAS_ID_15021,GWAS_ID_15022,GWAS_ID_15023,GWAS_ID_15024,GWAS_ID_15025,GWAS_ID_15026,GWAS_ID_15027,GWAS_ID_15028,GWAS_ID_15029,GWAS_ID_15030,GWAS_ID_15031,GWAS_ID_15032,GWAS_ID_15033,GWAS_ID_15034,GWAS_ID_15035,GWAS_ID_15036,GWAS_ID_15037,GWAS_ID_15038,GWAS_ID_15039,GWAS_ID_15040,GWAS_ID_15041,GWAS_ID_15042,GWAS_ID_15043,GWAS_ID_15044,GWAS_ID_15045,GWAS_ID_15046,GWAS_ID_15047,GWAS_ID_15048,GWAS_ID_15049,GWAS_ID_15050,GWAS_ID_15051,GWAS_ID_15052,GWAS_ID_15053,GWAS_ID_15054,GWAS_ID_15055,GWAS_ID_15056,GWAS_ID_15057,GWAS_ID_15058,GWAS_ID_15059,GWAS_ID_15060,GWAS_ID_15061,GWAS_ID_15062,GWAS_ID_15063,GWAS_ID_15064,GWAS_ID_15065,GWAS_ID_15066,GWAS_ID_15067,GWAS_ID_15068,GWAS_ID_15069,GWAS_ID_15070,GWAS_ID_15071,GWAS_ID_15072,GWAS_ID_15073,GWAS_ID_15074,GWAS_ID_15075,GWAS_ID_15076,GWAS_ID_15077,GWAS_ID_15078,GWAS_ID_15079,GWAS_ID_15080,GWAS_ID_15081,GWAS_ID_15082,GWAS_ID_15083,GWAS_ID_15084,GWAS_ID_15085,GWAS_ID_15086,GWAS_ID_15087,GWAS_ID_15088,GWAS_ID_15089,GWAS_ID_15090,GWAS_ID_15091,GWAS_ID_15092,GWAS_ID_15093,GWAS_ID_15094,GWAS_ID_15095,GWAS_ID_15096,GWAS_ID_15097,GWAS_ID_15098,GWAS_ID_15099,GWAS_ID_15100,GWAS_ID_15101,GWAS_ID_15102,GWAS_ID_15103,GWAS_ID_15104,GWAS_ID_15105,GWAS_ID_15106,GWAS_ID_15107,GWAS_ID_15108,GWAS_ID_15109,GWAS_ID_15110,GWAS_ID_15111,GWAS_ID_15112,GWAS_ID_15113,GWAS_ID_15114,GWAS_ID_15115,GWAS_ID_15116,GWAS_ID_15117,GWAS_ID_15118,GWAS_ID_15119,GWAS_ID_15120,GWAS_ID_15121,GWAS_ID_15122,GWAS_ID_15123,GWAS_ID_15124,GWAS_ID_15125,GWAS_ID_15126,GWAS_ID_15127,GWAS_ID_15128,GWAS_ID_15129,GWAS_ID_15130,GWAS_ID_15131,GWAS_ID_15132,GWAS_ID_15133,GWAS_ID_15134,GWAS_ID_15135,GWAS_ID_15136,GWAS_ID_15137,GWAS_ID_15138,GWAS_ID_15139,GWAS_ID_15140,GWAS_ID_15141,GWAS_ID_15142,GWAS_ID_15143,GWAS_ID_15144,GWAS_ID_15145,GWAS_ID_15146,GWAS_ID_15147,GWAS_ID_15148,GWAS_ID_15149,GWAS_ID_15150,GWAS_ID_15151,GWAS_ID_15152,GWAS_ID_15153,GWAS_ID_15154,GWAS_ID_15155,GWAS_ID_15156,GWAS_ID_15157,GWAS_ID_15158,GWAS_ID_15159,GWAS_ID_15160,GWAS_ID_15161,GWAS_ID_15162,GWAS_ID_15163,GWAS_ID_15164,GWAS_ID_15165,GWAS_ID_15166,GWAS_ID_15167,GWAS_ID_15168,GWAS_ID_15169,GWAS_ID_15170,GWAS_ID_15171,GWAS_ID_15172,GWAS_ID_15173,GWAS_ID_15174,GWAS_ID_15175,GWAS_ID_15176,GWAS_ID_15177,GWAS_ID_15178,GWAS_ID_15179,GWAS_ID_15180,GWAS_ID_15181,GWAS_ID_15182,GWAS_ID_15183,GWAS_ID_15184,GWAS_ID_15185,GWAS_ID_15186,GWAS_ID_15187,GWAS_ID_15188,GWAS_ID_15189,GWAS_ID_15190,GWAS_ID_15191,GWAS_ID_15192,GWAS_ID_15193,GWAS_ID_15194,GWAS_ID_15195,GWAS_ID_15196,GWAS_ID_15197,GWAS_ID_15198,GWAS_ID_15199,GWAS_ID_15200,GWAS_ID_15201,GWAS_ID_15202,GWAS_ID_15203,GWAS_ID_15204,GWAS_ID_15205,GWAS_ID_15206,GWAS_ID_15207 RMVar_hsa_circ_99289,RMVar_hsa_circ_101021,RMVar_hsa_circ_209623,RMVar_hsa_circ_209624 108080 RMVar_ID_108080 Human_SNP_ID_679687838 m1A Human chr20 - 35002781 35002781 35002781 CCAGAGTGGGGAGGAAGATATGGGTGACCCCCACCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC CCAGAGTGGGGAGGAAGATATGGGTGACCCCCGCCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC T C TRPC4AP Ensembl:ENSG00000100991 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5323221,Human_RBP_ID_8857485,Human_RBP_ID_17970310,Human_RBP_ID_23212290,Human_RBP_ID_26493018 Human_miRNA_ID_2691194 GWAS_ID_14852,GWAS_ID_14853,GWAS_ID_14854,GWAS_ID_14855,GWAS_ID_14856,GWAS_ID_14857,GWAS_ID_14858,GWAS_ID_14859,GWAS_ID_14860,GWAS_ID_14861,GWAS_ID_14862,GWAS_ID_14863,GWAS_ID_14864,GWAS_ID_14865,GWAS_ID_14866,GWAS_ID_14867,GWAS_ID_14868,GWAS_ID_14869,GWAS_ID_14870,GWAS_ID_14871,GWAS_ID_14872,GWAS_ID_14873,GWAS_ID_14874,GWAS_ID_14875,GWAS_ID_14876,GWAS_ID_14877,GWAS_ID_14878,GWAS_ID_14879,GWAS_ID_14880,GWAS_ID_14881,GWAS_ID_14882,GWAS_ID_14883,GWAS_ID_14884,GWAS_ID_14885,GWAS_ID_14886,GWAS_ID_14887,GWAS_ID_14888,GWAS_ID_14889,GWAS_ID_14890,GWAS_ID_14891,GWAS_ID_14892,GWAS_ID_14893,GWAS_ID_14894,GWAS_ID_14895,GWAS_ID_14896,GWAS_ID_14897,GWAS_ID_14898,GWAS_ID_14899,GWAS_ID_14900,GWAS_ID_14901,GWAS_ID_14902,GWAS_ID_14903,GWAS_ID_14904,GWAS_ID_14905,GWAS_ID_14906,GWAS_ID_14907,GWAS_ID_14908,GWAS_ID_14909,GWAS_ID_14910,GWAS_ID_14911,GWAS_ID_14912,GWAS_ID_14913,GWAS_ID_14914,GWAS_ID_14915,GWAS_ID_14916,GWAS_ID_14917,GWAS_ID_14918,GWAS_ID_14919,GWAS_ID_14920,GWAS_ID_14921,GWAS_ID_14922,GWAS_ID_14923,GWAS_ID_14924,GWAS_ID_14925,GWAS_ID_14926,GWAS_ID_14927,GWAS_ID_14928,GWAS_ID_14929,GWAS_ID_14930,GWAS_ID_14931,GWAS_ID_14932,GWAS_ID_14933,GWAS_ID_14934,GWAS_ID_14935,GWAS_ID_14936,GWAS_ID_14937,GWAS_ID_14938,GWAS_ID_14939,GWAS_ID_14940,GWAS_ID_14941,GWAS_ID_14942,GWAS_ID_14943,GWAS_ID_14944,GWAS_ID_14945,GWAS_ID_14946,GWAS_ID_14947,GWAS_ID_14948,GWAS_ID_14949,GWAS_ID_14950,GWAS_ID_14951,GWAS_ID_14952,GWAS_ID_14953,GWAS_ID_14954,GWAS_ID_14955,GWAS_ID_14956,GWAS_ID_14957,GWAS_ID_14958,GWAS_ID_14959,GWAS_ID_14960,GWAS_ID_14961,GWAS_ID_14962,GWAS_ID_14963,GWAS_ID_14964,GWAS_ID_14965,GWAS_ID_14966,GWAS_ID_14967,GWAS_ID_14968,GWAS_ID_14969,GWAS_ID_14970,GWAS_ID_14971,GWAS_ID_14972,GWAS_ID_14973,GWAS_ID_14974,GWAS_ID_14975,GWAS_ID_14976,GWAS_ID_14977,GWAS_ID_14978,GWAS_ID_14979,GWAS_ID_14980,GWAS_ID_14981,GWAS_ID_14982,GWAS_ID_14983,GWAS_ID_14984,GWAS_ID_14985,GWAS_ID_14986,GWAS_ID_14987,GWAS_ID_14988,GWAS_ID_14989,GWAS_ID_14990,GWAS_ID_14991,GWAS_ID_14992,GWAS_ID_14993,GWAS_ID_14994,GWAS_ID_14995,GWAS_ID_14996,GWAS_ID_14997,GWAS_ID_14998,GWAS_ID_14999,GWAS_ID_15000,GWAS_ID_15001,GWAS_ID_15002,GWAS_ID_15003,GWAS_ID_15004,GWAS_ID_15005,GWAS_ID_15006,GWAS_ID_15007,GWAS_ID_15008,GWAS_ID_15009,GWAS_ID_15010,GWAS_ID_15011,GWAS_ID_15012,GWAS_ID_15013,GWAS_ID_15014,GWAS_ID_15015,GWAS_ID_15016,GWAS_ID_15017,GWAS_ID_15018,GWAS_ID_15019,GWAS_ID_15020,GWAS_ID_15021,GWAS_ID_15022,GWAS_ID_15023,GWAS_ID_15024,GWAS_ID_15025,GWAS_ID_15026,GWAS_ID_15027,GWAS_ID_15028,GWAS_ID_15029,GWAS_ID_15030,GWAS_ID_15031,GWAS_ID_15032,GWAS_ID_15033,GWAS_ID_15034,GWAS_ID_15035,GWAS_ID_15036,GWAS_ID_15037,GWAS_ID_15038,GWAS_ID_15039,GWAS_ID_15040,GWAS_ID_15041,GWAS_ID_15042,GWAS_ID_15043,GWAS_ID_15044,GWAS_ID_15045,GWAS_ID_15046,GWAS_ID_15047,GWAS_ID_15048,GWAS_ID_15049,GWAS_ID_15050,GWAS_ID_15051,GWAS_ID_15052,GWAS_ID_15053,GWAS_ID_15054,GWAS_ID_15055,GWAS_ID_15056,GWAS_ID_15057,GWAS_ID_15058,GWAS_ID_15059,GWAS_ID_15060,GWAS_ID_15061,GWAS_ID_15062,GWAS_ID_15063,GWAS_ID_15064,GWAS_ID_15065,GWAS_ID_15066,GWAS_ID_15067,GWAS_ID_15068,GWAS_ID_15069,GWAS_ID_15070,GWAS_ID_15071,GWAS_ID_15072,GWAS_ID_15073,GWAS_ID_15074,GWAS_ID_15075,GWAS_ID_15076,GWAS_ID_15077,GWAS_ID_15078,GWAS_ID_15079,GWAS_ID_15080,GWAS_ID_15081,GWAS_ID_15082,GWAS_ID_15083,GWAS_ID_15084,GWAS_ID_15085,GWAS_ID_15086,GWAS_ID_15087,GWAS_ID_15088,GWAS_ID_15089,GWAS_ID_15090,GWAS_ID_15091,GWAS_ID_15092,GWAS_ID_15093,GWAS_ID_15094,GWAS_ID_15095,GWAS_ID_15096,GWAS_ID_15097,GWAS_ID_15098,GWAS_ID_15099,GWAS_ID_15100,GWAS_ID_15101,GWAS_ID_15102,GWAS_ID_15103,GWAS_ID_15104,GWAS_ID_15105,GWAS_ID_15106,GWAS_ID_15107,GWAS_ID_15108,GWAS_ID_15109,GWAS_ID_15110,GWAS_ID_15111,GWAS_ID_15112,GWAS_ID_15113,GWAS_ID_15114,GWAS_ID_15115,GWAS_ID_15116,GWAS_ID_15117,GWAS_ID_15118,GWAS_ID_15119,GWAS_ID_15120,GWAS_ID_15121,GWAS_ID_15122,GWAS_ID_15123,GWAS_ID_15124,GWAS_ID_15125,GWAS_ID_15126,GWAS_ID_15127,GWAS_ID_15128,GWAS_ID_15129,GWAS_ID_15130,GWAS_ID_15131,GWAS_ID_15132,GWAS_ID_15133,GWAS_ID_15134,GWAS_ID_15135,GWAS_ID_15136,GWAS_ID_15137,GWAS_ID_15138,GWAS_ID_15139,GWAS_ID_15140,GWAS_ID_15141,GWAS_ID_15142,GWAS_ID_15143,GWAS_ID_15144,GWAS_ID_15145,GWAS_ID_15146,GWAS_ID_15147,GWAS_ID_15148,GWAS_ID_15149,GWAS_ID_15150,GWAS_ID_15151,GWAS_ID_15152,GWAS_ID_15153,GWAS_ID_15154,GWAS_ID_15155,GWAS_ID_15156,GWAS_ID_15157,GWAS_ID_15158,GWAS_ID_15159,GWAS_ID_15160,GWAS_ID_15161,GWAS_ID_15162,GWAS_ID_15163,GWAS_ID_15164,GWAS_ID_15165,GWAS_ID_15166,GWAS_ID_15167,GWAS_ID_15168,GWAS_ID_15169,GWAS_ID_15170,GWAS_ID_15171,GWAS_ID_15172,GWAS_ID_15173,GWAS_ID_15174,GWAS_ID_15175,GWAS_ID_15176,GWAS_ID_15177,GWAS_ID_15178,GWAS_ID_15179,GWAS_ID_15180,GWAS_ID_15181,GWAS_ID_15182,GWAS_ID_15183,GWAS_ID_15184,GWAS_ID_15185,GWAS_ID_15186,GWAS_ID_15187,GWAS_ID_15188,GWAS_ID_15189,GWAS_ID_15190,GWAS_ID_15191,GWAS_ID_15192,GWAS_ID_15193,GWAS_ID_15194,GWAS_ID_15195,GWAS_ID_15196,GWAS_ID_15197,GWAS_ID_15198,GWAS_ID_15199,GWAS_ID_15200,GWAS_ID_15201,GWAS_ID_15202,GWAS_ID_15203,GWAS_ID_15204,GWAS_ID_15205,GWAS_ID_15206,GWAS_ID_15207 RMVar_hsa_circ_99289,RMVar_hsa_circ_101021,RMVar_hsa_circ_209623,RMVar_hsa_circ_209624 108081 RMVar_ID_108081 Human_SNP_ID_679688423 m1A Human chr20 - 35004511 35004511 35004511 TGCTCGCCTACATATCCCAGGTGCCCACGCAGATGTCCTTCCTCTTCCGCCTCATCAACATCATC TGCTCGCCTACATATCCCAGGTGCCCACGCAGCTGTCCTTCCTCTTCCGCCTCATCAACATCATC T G TRPC4AP Ensembl:ENSG00000100991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35004427..35004584 26863196 MeRIP-seq:(Medium) rs775195020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9390402 Human_Splice_Rec_2075550,Human_Splice_Rec_2075551,Human_Splice_Rec_2075586,Human_Splice_Rec_2075587 RMVar_hsa_circ_36740,RMVar_hsa_circ_101021,RMVar_hsa_circ_125323,RMVar_hsa_circ_209624,RMVar_hsa_circ_121515,RMVar_hsa_circ_36703,RMVar_hsa_circ_209625,RMVar_hsa_circ_209626,RMVar_hsa_circ_63308,RMVar_hsa_circ_283872,RMVar_hsa_circ_209627,RMVar_hsa_circ_209628 108082 RMVar_ID_108082 Human_SNP_ID_679700924 m1A Human chr20 - 35051853 35051853 35051853 GGAGTAGCACTTTGATAAATTGAAGAGAGGAGAAAGGTGGGTAGTCAAGGGTAGCTAGTTAGAGC GGAGTAGCACTTTGATAAATTGAAGAGAGGAGCAAGGTGGGTAGTCAAGGGTAGCTAGTTAGAGC T G TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35051851..35051933 26863196 MeRIP-seq:(Medium) rs973269034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_20011,RMVar_hsa_circ_11875,RMVar_hsa_circ_325101,RMVar_hsa_circ_46591,RMVar_hsa_circ_209644,RMVar_hsa_circ_285798,RMVar_hsa_circ_363596,RMVar_hsa_circ_279326,RMVar_hsa_circ_209646,RMVar_hsa_circ_209647,RMVar_hsa_circ_57302,RMVar_hsa_circ_305976,RMVar_hsa_circ_349966,RMVar_hsa_circ_209648 108083 RMVar_ID_108083 Human_SNP_ID_679712384 m1A Human chr20 + 35092710 35092691 35092710 CCAGGCCGCGGCCGGCCGCCCCATCCGCCCCAAGCCGCCACTGTGGCTGCCGACCGTCTCCCTCG CCAGGCCGCGGCCG___________________GCCGCCACTGTGGCTGCCGACCGTCTCCCTCG GGCCGCCCCATCCGCCCCAA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:35092637..35092775 26863196 MeRIP-seq:(Medium) rs746964373 Functional Loss DEL dbSNP153 15..33 33 - - - 108084 RMVar_ID_108084 Human_SNP_ID_679719108 m1A Human chr20 - 35116471 35116471 35116471 CCCGAAGCAGGAGGGTGCTGTGCTAGCTCAGGACAGAAAGGCAGCAGCTGGAGCTCTTAGAGTGG CCCGAAGCAGGAGGGTGCTGTGCTAGCTCAGGGCAGAAAGGCAGCAGCTGGAGCTCTTAGAGTGG T C EDEM2 Ensembl:ENSG00000088298 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35116469..35116576 26863196 MeRIP-seq:(Medium) rs931899017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6994001 108085 RMVar_ID_108085 Human_SNP_ID_679719114 m1A Human chr20 - 35116495 35116495 35116495 TGAAAGAACCACAGATGCAAAGAGCCCGAAGCAGGAGGGTGCTGTGCTAGCTCAGGACAGAAAGG TGAAAGAACCACAGATGCAAAGAGCCCGAAGCGGGAGGGTGCTGTGCTAGCTCAGGACAGAAAGG T C EDEM2 Ensembl:ENSG00000088298 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35116489..35116583 26863196 MeRIP-seq:(Medium) rs1036189121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6994001 108086 RMVar_ID_108086 Human_SNP_ID_679726541 m1A Human chr20 - 35147040 35147040 35147040 CCCGACTTGCTCCGACACAGCCGCTAGGTCCCAGGGAGAAATCAGCTAGTGATTCCCACTTTCCG CCCGACTTGCTCCGACACAGCCGCTAGGTCCCCGGGAGAAATCAGCTAGTGATTCCCACTTTCCG T G EDEM2 Ensembl:ENSG00000088298 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:35147039..35147184 26863196 MeRIP-seq:(Medium) rs1216789143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2667335 RMVar_hsa_circ_117137,RMVar_hsa_circ_114291,RMVar_hsa_circ_209656,RMVar_hsa_circ_209657 108087 RMVar_ID_108087 Human_SNP_ID_679745692 m1A Human chr20 + 35225499 35225499 35225499 TGCTTAAACACACACATACACACACACACACCACACACACACAACCTTTAATGACCACCCTCCCC TGCTTAAACACACACATACACACACACACACCCCACACACACAACCTTTAATGACCACCCTCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35225496..35225711 26863196 MeRIP-seq:(Medium) rs1568606142 Functional Loss SNV dbSNP153 33..33 33 - - - 108088 RMVar_ID_108088 Human_SNP_ID_679754144 m1A Human chr20 + 35263506 35263506 35263506 CTTTGTGAAGCTTTCCCTGAACATCTTCCTCCAGGTTTAAATGACCCCTCTCTCCTCAGAATCCC CTTTGTGAAGCTTTCCCTGAACATCTTCCTCCGGGTTTAAATGACCCCTCTCTCCTCAGAATCCC A G MMP24 Ensembl:ENSG00000125966 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35263459..35263587 26863196 MeRIP-seq:(Medium) rs1050724557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7088,RMVar_hsa_circ_378284,RMVar_hsa_circ_102184,RMVar_hsa_circ_11810,RMVar_hsa_circ_125312,RMVar_hsa_circ_209663,RMVar_hsa_circ_209664,RMVar_hsa_circ_209665,RMVar_hsa_circ_209662,RMVar_hsa_circ_209666,RMVar_hsa_circ_209669 108089 RMVar_ID_108089 Human_SNP_ID_679755832 m1A Human chr20 + 35269410 35269410 35269410 CGGCCCAGGCTCAGTGACCACCCCAGCCTCCCACTGTCCCGAGGACCAGTCTGGCTGATGTCAGT CGGCCCAGGCTCAGTGACCACCCCAGCCTCCCGCTGTCCCGAGGACCAGTCTGGCTGATGTCAGT A G MMP24 Ensembl:ENSG00000125966 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35269408..35269507 26863196 MeRIP-seq:(Medium) rs907644206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7088,RMVar_hsa_circ_378284,RMVar_hsa_circ_125312,RMVar_hsa_circ_209664,RMVar_hsa_circ_209665,RMVar_hsa_circ_209666,RMVar_hsa_circ_34550 108090 RMVar_ID_108090 Human_SNP_ID_679757759 m1A Human chr20 - 35276612 35276612 35276612 TCAAGAAGTGAGAGCACCAACCTGAGGAGTGGACAGGGACCAGGAAGTGGGGGAAGGGAGGCCAG TCAAGAAGTGAGAGCACCAACCTGAGGAGTGGGCAGGGACCAGGAAGTGGGGGAAGGGAGGCCAG T C AL121753.1,MMP24OS Ensembl:ENSG00000261582,Ensembl:ENSG00000126005 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35276466..35276864 32194978 MeRIP-seq:(Medium) rs1472026554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3646985,Human_RBP_ID_14081997,Human_RBP_ID_23901763 108091 RMVar_ID_108091 Human_SNP_ID_679758271 m1A Human chr20 + 35278061 35278061 35278061 GGTCTCCCGGAACCCACCTCGGCGTCGGGAGGAGCTGGCGCCGTGACGCCACCACCGCGTACCGA GGTCTCCCGGAACCCACCTCGGCGTCGGGAGGGGCTGGCGCCGTGACGCCACCACCGCGTACCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:35277317..35278125;chr20:35277801..35278125 26863196 MeRIP-seq:(Medium) rs1467709735 Functional Loss SNV dbSNP153 33..33 33 - - - 108092 RMVar_ID_108092 Human_SNP_ID_679758285 m1A Human chr20 - 35278096 35278096 35278096 TCCCTTCTTTCCGCTCCAACGCACGGAGGGTGAGGTCGGTACGCGGTGGTGGCGTCACGGCGCCA TCCCTTCTTTCCGCTCCAACGCACGGAGGGTGGGGTCGGTACGCGGTGGTGGCGTCACGGCGCCA T C AL121753.1,MMP24OS Ensembl:ENSG00000261582,Ensembl:ENSG00000126005 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35277997..35278125 26863196 MeRIP-seq:(Medium) rs12481346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659767,Human_RBP_ID_5384995,Human_RBP_ID_14082015 Human_Splice_Rec_2075643,Human_Splice_Rec_2075651,Human_Splice_Rec_2075657,Human_Splice_Rec_2075663,Human_Splice_Rec_2075667,Human_Splice_Rec_2075673,Human_Splice_Rec_2075679,Human_Splice_Rec_2075683,Human_Splice_Rec_2075685,Human_Splice_Rec_2075689 108093 RMVar_ID_108093 Human_SNP_ID_679758914 m1A Human chr20 - 35280117 35280117 35280117 GAGCCCTGAACACAATATCTTTGATTGACAGGAGACAGAAGAAATTCTGGCAGATGTGCTCAAGG GAGCCCTGAACACAATATCTTTGATTGACAGGTGACAGAAGAAATTCTGGCAGATGTGCTCAAGG T A EIF6 Ensembl:ENSG00000242372 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35280073..35280144 26863196 MeRIP-seq:(Medium) rs754043227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2682460,Human_RBP_ID_4643399,Human_RBP_ID_22671957 Human_Splice_Rec_2075714,Human_Splice_Rec_2075724,Human_Splice_Rec_2075732,Human_Splice_Rec_2075742,Human_Splice_Rec_2075754,Human_Splice_Rec_2075764,Human_Splice_Rec_2075770 RMVar_hsa_circ_209672,RMVar_hsa_circ_119764,RMVar_hsa_circ_95804,RMVar_hsa_circ_103158,RMVar_hsa_circ_105121,RMVar_hsa_circ_101492,RMVar_hsa_circ_209674,RMVar_hsa_circ_209676,RMVar_hsa_circ_86203,RMVar_hsa_circ_209677,RMVar_hsa_circ_209675,RMVar_hsa_circ_209673,RMVar_hsa_circ_6981,RMVar_hsa_circ_336458,RMVar_hsa_circ_348201,RMVar_hsa_circ_113546,RMVar_hsa_circ_209678,RMVar_hsa_circ_209679,RMVar_hsa_circ_209680,RMVar_hsa_circ_376172 108094 RMVar_ID_108094 Human_SNP_ID_679759088 m1A Human chr20 - 35280831 35280831 35280831 TTGTGTATTCACCCTCTAATTTGGGTTTCTCCAGGGAACAGGCACGGTCTCCTGGTACCCAACAA TTGTGTATTCACCCTCTAATTTGGGTTTCTCCTGGGAACAGGCACGGTCTCCTGGTACCCAACAA T A EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35280801..35280850 32194978 MeRIP-seq:(Medium) rs111473239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926799,Human_RBP_ID_4643407 RMVar_hsa_circ_119764,RMVar_hsa_circ_95804,RMVar_hsa_circ_103158,RMVar_hsa_circ_209674,RMVar_hsa_circ_209676,RMVar_hsa_circ_86203,RMVar_hsa_circ_209677,RMVar_hsa_circ_209675,RMVar_hsa_circ_336458,RMVar_hsa_circ_113546,RMVar_hsa_circ_209678,RMVar_hsa_circ_209679 108095 RMVar_ID_108095 Human_SNP_ID_679759089 m1A Human chr20 - 35280831 35280831 35280831 TTGTGTATTCACCCTCTAATTTGGGTTTCTCCAGGGAACAGGCACGGTCTCCTGGTACCCAACAA TTGTGTATTCACCCTCTAATTTGGGTTTCTCCGGGGAACAGGCACGGTCTCCTGGTACCCAACAA T C EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35280801..35280850 32194978 MeRIP-seq:(Medium) rs111473239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926799,Human_RBP_ID_4643407 RMVar_hsa_circ_119764,RMVar_hsa_circ_95804,RMVar_hsa_circ_103158,RMVar_hsa_circ_209674,RMVar_hsa_circ_209676,RMVar_hsa_circ_86203,RMVar_hsa_circ_209677,RMVar_hsa_circ_209675,RMVar_hsa_circ_336458,RMVar_hsa_circ_113546,RMVar_hsa_circ_209678,RMVar_hsa_circ_209679 108096 RMVar_ID_108096 Human_SNP_ID_679760193 m1A Human chr20 + 35284575 35284575 35284575 ATCCCGGCCTCCGTCCCTCAGGCCCCGCCGCGACCCCGCCCCTCTCGGCCTCCCGGCCCCTCCGT ATCCCGGCCTCCGTCCCTCAGGCCCCGCCGCGCCCCCGCCCCTCTCGGCCTCCCGGCCCCTCCGT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:35284551..35284700 26863196 MeRIP-seq:(Medium) rs888943220 Functional Loss SNV dbSNP153 33..33 33 - - - 108097 RMVar_ID_108097 Human_SNP_ID_679760393 m1A Human chr20 + 35285251 35285251 35285251 AGGCTACCCATGGAGAGAGTTCCAGGAGGCAGAAGTGCGGCCAGACCGAGGCTGGAGAAAGAGCG AGGCTACCCATGGAGAGAGTTCCAGGAGGCAGCAGTGCGGCCAGACCGAGGCTGGAGAAAGAGCG A C FAM83C-AS1 Ensembl:ENSG00000235214 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35285206..35285340 26863196 MeRIP-seq:(Medium) rs1453176187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2075777 108098 RMVar_ID_108098 Human_SNP_ID_679765348 m1A Human chr20 - 35303017 35303017 35303017 TCCCCCTTCCCAACTTCTGAAGCACGTGCTGCAGAGCCACCTTGGTCTGAGCACCTGAGGACCAG TCCCCCTTCCCAACTTCTGAAGCACGTGCTGCCGAGCCACCTTGGTCTGAGCACCTGAGGACCAG T G UQCC1 Ensembl:ENSG00000101019 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35302967..35303055 26863196 MeRIP-seq:(Medium) rs1015411523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562510,Human_RBP_ID_6994144,Human_RBP_ID_14082177 108099 RMVar_ID_108099 Human_SNP_ID_679774821 m1A Human chr20 - 35346043 35346043 35346043 TGCATTTACAATCCTCTAGCTAGACACAGAGCACTGATTGGTGCAAGTATCCACCCGACCCAGAA TGCATTTACAATCCTCTAGCTAGACACAGAGCGCTGATTGGTGCAAGTATCCACCCGACCCAGAA T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6142349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14082907,Human_RBP_ID_23901894 RMVar_hsa_circ_316254,RMVar_hsa_circ_344263,RMVar_hsa_circ_323431 108100 RMVar_ID_108100 Human_SNP_ID_679801701 m1A Human chr20 + 35455227 35455227 35455227 AATCGCGGAGCAACTAGCCGGGCGTCTGCGGGAGCCGAGCGTGGTGAGGTGGGGCCTCAGGGGCA AATCGCGGAGCAACTAGCCGGGCGTCTGCGGGTGCCGAGCGTGGTGAGGTGGGGCCTCAGGGGCA A T CEP250 Ensembl:ENSG00000126001 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35455177..35455650 26863196 MeRIP-seq:(Medium) rs1259656794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659352,Human_RBP_ID_18422868 Human_Splice_Rec_2076053,Human_Splice_Rec_2076065 108101 RMVar_ID_108101 Human_SNP_ID_679801783 m1A Human chr20 + 35455494 35455494 35455494 CGAAGGAGAGCTTCCCGACCCTCGTGTCCAGTAGCCGCAATCCCAGGCTGGGAGGGTGAGGCGCC CGAAGGAGAGCTTCCCGACCCTCGTGTCCAGTGGCCGCAATCCCAGGCTGGGAGGGTGAGGCGCC A G CEP250 Ensembl:ENSG00000126001 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35455463..35455564 26863196 MeRIP-seq:(Medium) rs1464348105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2076077 108102 RMVar_ID_108102 Human_SNP_ID_679804209 m1A Human chr20 - 35466077 35466077 35466077 CTTTATTCACCACGTCAGCTTTTTCCATGTGCAGTCGAAGCTGGGTGTTCACCTCTGCTAGACTC CTTTATTCACCACGTCAGCTTTTTCCATGTGCGGTCGAAGCTGGGTGTTCACCTCTGCTAGACTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35465814..35466988 26863196 MeRIP-seq:(Medium) rs1276104668 Functional Loss SNV dbSNP153 33..33 33 - - - 108103 RMVar_ID_108103 Human_SNP_ID_679804226 m1A Human chr20 + 35466161 35466157 35466162 AAAACTGACAGTGGACTGGAGCCGGGCCCGGGATGAGCTAATGAGGAAGGAGAGCCAGTGGCAGA AAAACTGACAGTGGACTGGAGCCGGGCCC_____GAGCTAATGAGGAAGGAGAGCCAGTGGCAGA CGGGAT C CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35466026..35466225 26863196 MeRIP-seq:(Medium) rs1568759172 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_244454,Human_RBP_ID_831930,Human_RBP_ID_924853,Human_RBP_ID_3960731,Human_RBP_ID_6994635,Human_RBP_ID_8857334,Human_RBP_ID_9389055,Human_RBP_ID_14084501,Human_RBP_ID_18471097,Human_RBP_ID_19004085,Human_RBP_ID_22081626,Human_RBP_ID_26342853 Human_Splice_Rec_2076093,Human_Splice_Rec_2076123,Human_Splice_Rec_2076191,Human_Splice_Rec_2076203,Human_Splice_Rec_2076225 RMVar_hsa_circ_30687,RMVar_hsa_circ_67116,RMVar_hsa_circ_50287,RMVar_hsa_circ_317066,RMVar_hsa_circ_363819 108104 RMVar_ID_108104 Human_SNP_ID_679807104 m1A Human chr20 + 35478013 35478013 35478013 GGAAAAGAACACTCACCTGGAGGCTCAGCTGCAGAAAGCTGAGGAGGCTGGGGCTGAGCTGCAGG GGAAAAGAACACTCACCTGGAGGCTCAGCTGCGGAAAGCTGAGGAGGCTGGGGCTGAGCTGCAGG A G CEP250 Ensembl:ENSG00000126001 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35477887..35480143 26863196 MeRIP-seq:(Medium) rs143077635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960737,Human_RBP_ID_5471803,Human_RBP_ID_8853952,Human_RBP_ID_19004095,Human_RBP_ID_26343548,Human_RBP_ID_27819691 Human_Splice_Rec_2076143 RMVar_hsa_circ_30687,RMVar_hsa_circ_67116,RMVar_hsa_circ_63070,RMVar_hsa_circ_291042 108105 RMVar_ID_108105 Human_SNP_ID_679807411 m1A Human chr20 + 35479255 35479255 35479255 CCCCTCAGTCACGTCACCAGCAGGAGGCAGCCACGACTCAGCTGGAGCAGCTACATCAGGAGGCA CCCCTCAGTCACGTCACCAGCAGGAGGCAGCCTCGACTCAGCTGGAGCAGCTACATCAGGAGGCA A T CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:35477931..35479741;chr20:35477884..35490784 26863196 MeRIP-seq:(Medium) rs1164965091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924464,Human_RBP_ID_8234972,Human_RBP_ID_9390438,Human_RBP_ID_19005502,Human_RBP_ID_24546650,Human_RBP_ID_26342865,Human_RBP_ID_27819693 Human_Splice_Rec_2076144 RMVar_hsa_circ_67116,RMVar_hsa_circ_209695,RMVar_hsa_circ_284826 108106 RMVar_ID_108106 Human_SNP_ID_679811144 m1A Human chr20 + 35494602 35494602 35494602 GGCTGGTGGAGCAGGAGGTTCAGGAGAAGCTGAGAGAGACCCAGGAGTATAACCGAATTCAGAAG GGCTGGTGGAGCAGGAGGTTCAGGAGAAGCTGCGAGAGACCCAGGAGTATAACCGAATTCAGAAG A C CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35494526..35494631 26863196 MeRIP-seq:(Medium) rs1384739611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3960742,Human_RBP_ID_9298452,Human_RBP_ID_9389083,Human_RBP_ID_17976501,Human_RBP_ID_19005515,Human_RBP_ID_26342428 Human_Splice_Rec_2076156,Human_Splice_Rec_2076157,Human_Splice_Rec_2076241 Human_miRNA_ID_2041640,Human_miRNA_ID_3020618 RMVar_hsa_circ_284778,RMVar_hsa_circ_41996,RMVar_hsa_circ_64776,RMVar_hsa_circ_347614,RMVar_hsa_circ_361800 108107 RMVar_ID_108107 Human_SNP_ID_679813131 m1A Human chr20 + 35502614 35502614 35502614 CTGCAAGAGCAGGGCGAACTGAAGGTGGCCCAAGGGAAGGCTCTGCAAGAGAATTTGGCCCTCCT CTGCAAGAGCAGGGCGAACTGAAGGTGGCCCAGGGGAAGGCTCTGCAAGAGAATTTGGCCCTCCT A G CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35502565..35502651 26863196 MeRIP-seq:(Medium) rs1299522231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4643682,Human_RBP_ID_9298456,Human_RBP_ID_26342881 RMVar_hsa_circ_347614,RMVar_hsa_circ_361800,RMVar_hsa_circ_359052 108108 RMVar_ID_108108 Human_SNP_ID_679813288 m1A Human chr20 - 35503105 35503105 35503105 AAGCCACTCTCTGGGTTTCCCTCTGGCCCTCCAGCTCCTTGATCAGTTTTTGCTGGCACTCCATC AAGCCACTCTCTGGGTTTCCCTCTGGCCCTCCTGCTCCTTGATCAGTTTTTGCTGGCACTCCATC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35503055..35503206 32194978 MeRIP-seq:(Medium) rs1399342319 Functional Loss SNV dbSNP153 33..33 33 - - - 108109 RMVar_ID_108109 Human_SNP_ID_679813413 m1A Human chr20 + 35503476 35503476 35503476 TGAGAGAGCGAGGCCGGGAGCTGACCACTCAGAGGCAGCTGATGCAGGAACGGGCAGAGGAAGGG TGAGAGAGCGAGGCCGGGAGCTGACCACTCAGTGGCAGCTGATGCAGGAACGGGCAGAGGAAGGG A T CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35503426..35503628 26863196 MeRIP-seq:(Medium) rs1293253583 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22722924 Human_miRNA_ID_2242510 RMVar_hsa_circ_347614,RMVar_hsa_circ_361800,RMVar_hsa_circ_359052 108110 RMVar_ID_108110 Human_SNP_ID_679813595 m1A Human chr20 - 35503999 35503999 35503999 CCTCCTCCAGGGCCTGGACCCGCCGTCCCTCCACTGCCAGCTCTTCCTCCAGCCTTCGTGCCTGT CCTCCTCCAGGGCCTGGACCCGCCGTCCCTCCGCTGCCAGCTCTTCCTCCAGCCTTCGTGCCTGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35503226..35504255 26863196 MeRIP-seq:(Medium) rs781479758 Functional Loss SNV dbSNP153 33..33 33 - - - 108111 RMVar_ID_108111 Human_SNP_ID_679814797 m1A Human chr20 - 35508182 35508182 35508182 CCACTGGACAAGAAGAGGGGTCACCTGCTCCAAGGTACTCCGCAGCTGGACATTGTGGCGCTGCA CCACTGGACAAGAAGAGGGGTCACCTGCTCCAGGGTACTCCGCAGCTGGACATTGTGGCGCTGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35503305..35511883 32194978 MeRIP-seq:(Medium) rs535604273 Functional Loss SNV dbSNP153 33..33 33 - - - 108112 RMVar_ID_108112 Human_SNP_ID_679824887 m1A Human chr20 - 35546269 35546267 35546269 ATTTCTCAGCTCTCCCTTACAGTGAAACTCCCAAGTCACCTATAGGTAATGTCTCCACTTCCTTT ATTTCTCAGCTCTCCCTTACAGTGAAACTCCC__GTCACCTATAGGTAATGTCTCCACTTCCTTT CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35546268..35546987 26863196 MeRIP-seq:(Medium) rs771844558 Functional Loss DEL dbSNP153 33..34 33 - - - 108113 RMVar_ID_108113 Human_SNP_ID_679825178 m1A Human chr20 - 35547488 35547488 35547488 TCCCCGCCAGCTCACTTGATATCTTCTGCCTCAGCACCATAGCAGCTCTCACAGCGATCAGGGTC TCCCCGCCAGCTCACTTGATATCTTCTGCCTCGGCACCATAGCAGCTCTCACAGCGATCAGGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35547369..35547557 26863196 MeRIP-seq:(Medium) rs768853849 Functional Loss SNV dbSNP153 33..33 33 - - - 108114 RMVar_ID_108114 Human_SNP_ID_679825439 m1A Human chr20 - 35548469 35548469 35548469 GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCATAAGTCCAGTGCTGGCATCTGGGGAAATAGAG GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCTTAAGTCCAGTGCTGGCATCTGGGGAAATAGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35548465..35548713 26863196 MeRIP-seq:(Medium) rs77272989 Functional Loss SNV dbSNP153 33..33 33 - - - 108115 RMVar_ID_108115 Human_SNP_ID_679825440 m1A Human chr20 - 35548469 35548469 35548469 GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCATAAGTCCAGTGCTGGCATCTGGGGAAATAGAG GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCGTAAGTCCAGTGCTGGCATCTGGGGAAATAGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35548465..35548713 26863196 MeRIP-seq:(Medium) rs77272989 Functional Loss SNV dbSNP153 33..33 33 - - - 108116 RMVar_ID_108116 Human_SNP_ID_679825441 m1A Human chr20 - 35548469 35548469 35548469 GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCATAAGTCCAGTGCTGGCATCTGGGGAAATAGAG GCAGGGAGTGACGGTGAGAGTGTTAAAGAGGCCTAAGTCCAGTGCTGGCATCTGGGGAAATAGAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35548465..35548713 26863196 MeRIP-seq:(Medium) rs77272989 Functional Loss SNV dbSNP153 33..33 33 - - - 108117 RMVar_ID_108117 Human_SNP_ID_679825455 m1A Human chr20 + 35548526 35548526 35548526 CTCCCTGCCCTACAGGTGCTGTAACACCTGTGAAGATGTGCGGGAGGCATATCGCCGTAGAGGCT CTCCCTGCCCTACAGGTGCTGTAACACCTGTGCAGATGTGCGGGAGGCATATCGCCGTAGAGGCT A C ERGIC3 Ensembl:ENSG00000125991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746564496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62845,Human_RBP_ID_562599,Human_RBP_ID_778997,Human_RBP_ID_1595688,Human_RBP_ID_3960191,Human_RBP_ID_5119350,Human_RBP_ID_9116515,Human_RBP_ID_17659315,Human_RBP_ID_17700358,Human_RBP_ID_17976333,Human_RBP_ID_18771710,Human_RBP_ID_19004110,Human_RBP_ID_22767298,Human_RBP_ID_24546850,Human_RBP_ID_26820798,Human_RBP_ID_27020018 Human_Splice_Rec_2076332,Human_Splice_Rec_2076356,Human_Splice_Rec_2076382,Human_Splice_Rec_2076416,Human_Splice_Rec_2076436,Human_Splice_Rec_2076464,Human_Splice_Rec_2076482,Human_Splice_Rec_2076490,Human_Splice_Rec_2076500,Human_Splice_Rec_2076504 Human_miRNA_ID_2778533 RMVar_hsa_circ_32149,RMVar_hsa_circ_305136,RMVar_hsa_circ_35436,RMVar_hsa_circ_334715 108118 RMVar_ID_108118 Human_SNP_ID_679826043 m1A Human chr20 + 35550759 35550759 35550759 GCCCTGAAGAAGGTGAGGCATGATCTGACTTAAAAGCTCTCCAGCTGCTCTGTGGACAAGACTGG GCCCTGAAGAAGGTGAGGCATGATCTGACTTATAAGCTCTCCAGCTGCTCTGTGGACAAGACTGG A T ERGIC3 Ensembl:ENSG00000125991 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35550755..35550950 26863196 MeRIP-seq:(Medium) rs1459882975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14084860 RMVar_hsa_circ_32149,RMVar_hsa_circ_35436 108119 RMVar_ID_108119 Human_SNP_ID_679826219 m1A Human chr20 + 35551527 35551526 35551527 TGCCTGGAGATGCAGATGTTGGCATCATCAGCATGTGTATAGAGCTGTGGGACTGGATGAAATCA TGCCTGGAGATGCAGATGTTGGCATCATCAGC_TGTGTATAGAGCTGTGGGACTGGATGAAATCA CA C ERGIC3 Ensembl:ENSG00000125991 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35551523..35551711 26863196 MeRIP-seq:(Medium) rs996189813 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1595693,Human_RBP_ID_14084888 RMVar_hsa_circ_32149,RMVar_hsa_circ_35436 108120 RMVar_ID_108120 Human_SNP_ID_679827887 m1A Human chr20 + 35557475 35557475 35557475 CGCTCATCTACCACTCAGCACGAGCCATCCAGAAGAAAATTGATCTAGGGAAGACAACGTAGTCA CGCTCATCTACCACTCAGCACGAGCCATCCAGGAGAAAATTGATCTAGGGAAGACAACGTAGTCA A G ERGIC3 Ensembl:ENSG00000125991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs756289386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562624,Human_RBP_ID_1595701,Human_RBP_ID_1928583,Human_RBP_ID_9116518,Human_RBP_ID_17659319,Human_RBP_ID_18193642,Human_RBP_ID_18771724,Human_RBP_ID_22767315,Human_RBP_ID_22817233,Human_RBP_ID_26821326 Human_Splice_Rec_2076346,Human_Splice_Rec_2076372,Human_Splice_Rec_2076432,Human_Splice_Rec_2076528,Human_Splice_Rec_2076536,Human_Splice_Rec_2076542,Human_Splice_Rec_2076546 RMVar_hsa_circ_91347,RMVar_hsa_circ_118312,RMVar_hsa_circ_209705,RMVar_hsa_circ_80229,RMVar_hsa_circ_209708,RMVar_hsa_circ_116216,RMVar_hsa_circ_209710,RMVar_hsa_circ_127137,RMVar_hsa_circ_209711,RMVar_hsa_circ_209712 108121 RMVar_ID_108121 Human_SNP_ID_679827911 m1A Human chr20 - 35557554 35557554 35557554 CCGAGGAGGTGGAGGGTGGCAGAGGCTGGGGGACAACCACAGGCCAGGGAGAAAGAGGAGACAGA CCGAGGAGGTGGAGGGTGGCAGAGGCTGGGGGGCAACCACAGGCCAGGGAGAAAGAGGAGACAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35557481..35557625 26863196 MeRIP-seq:(Medium) rs113273063 Functional Loss SNV dbSNP153 33..33 33 - - - 108122 RMVar_ID_108122 Human_SNP_ID_679835964 m1A Human chr20 + 35584192 35584192 35584192 TCCTGCTTCCCCAGGGCACACCTCTACTGCACATCGCCACACCATGCCAAACTCCCAGTCCACTC TCCTGCTTCCCCAGGGCACACCTCTACTGCACGTCGCCACACCATGCCAAACTCCCAGTCCACTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35584145..35584389 26863196 MeRIP-seq:(Medium) rs1397266384 Functional Loss SNV dbSNP153 33..33 33 - - - 108123 RMVar_ID_108123 Human_SNP_ID_679843970 m1A Human chr20 - 35615911 35615911 35615911 GGGGCCTCCTTCAGCCGCTGCGCGCCGCGGGGACCCCACGGACCCTGCGTGAAGTCGGCAGGCCC GGGGCCTCCTTCAGCCGCTGCGCGCCGCGGGGGCCCCACGGACCCTGCGTGAAGTCGGCAGGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35615861..35616020 26863196 MeRIP-seq:(Medium) rs1180035753 Functional Loss SNV dbSNP153 33..33 33 - - - 108124 RMVar_ID_108124 Human_SNP_ID_679844205 m1A Human chr20 + 35616411 35616411 35616411 GGGGCTAAGATGATATCTGGGCACCTCCTACAAGGTGGGTCCTGTAGGGTAAAGGGATGGTGCTA GGGGCTAAGATGATATCTGGGCACCTCCTACAGGGTGGGTCCTGTAGGGTAAAGGGATGGTGCTA A G SPAG4 Ensembl:ENSG00000061656 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35616367..35616507 26863196 MeRIP-seq:(Medium) rs1393564668 Functional Loss SNV dbSNP153 33..33 33 - - - 108125 RMVar_ID_108125 Human_SNP_ID_679848420 m1A Human chr20 - 35630845 35630845 35630845 ATACCCGCTCCCTGCAGATGCTTCAGCCTCTGAGCTTACAGTCCCCTCACTGCCTTTTGCCCAAT ATACCCGCTCCCTGCAGATGCTTCAGCCTCTGCGCTTACAGTCCCCTCACTGCCTTTTGCCCAAT T G CPNE1 Ensembl:ENSG00000214078 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35630841..35630964 26863196 MeRIP-seq:(Medium) rs1194009195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5382616,Human_RBP_ID_14085418,Human_RBP_ID_22549183,Human_RBP_ID_24424597 RMVar_hsa_circ_47999,RMVar_hsa_circ_116446,RMVar_hsa_circ_21402,RMVar_hsa_circ_39545,RMVar_hsa_circ_209722,RMVar_hsa_circ_209724,RMVar_hsa_circ_123797,RMVar_hsa_circ_292159,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_278416,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727,RMVar_hsa_circ_209725,RMVar_hsa_circ_209723 108126 RMVar_ID_108126 Human_SNP_ID_679848615 m1A Human chr20 + 35631331 35631331 35631331 TTCTTGTAGCTTTTCTTTTTCTGCTGCTTCTCAGGGTGGATGCATTCAAACTCAGCCTGGTGAGG TTCTTGTAGCTTTTCTTTTTCTGCTGCTTCTCGGGGTGGATGCATTCAAACTCAGCCTGGTGAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35631247..35631383 26863196 MeRIP-seq:(Medium) rs759987488 Functional Loss SNV dbSNP153 33..33 33 - - - 108127 RMVar_ID_108127 Human_SNP_ID_679849058 m1A Human chr20 + 35632529 35632529 35632529 TAATCCCCAGCCCTACATACCTGTCCTAGGGAACACTCAGCACCCCCTAGGAAGTCATCATCCCT TAATCCCCAGCCCTACATACCTGTCCTAGGGATCACTCAGCACCCCCTAGGAAGTCATCATCCCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:35632526..35632550 32194978 MeRIP-seq:(Medium) rs1388842415 Functional Loss SNV dbSNP153 33..33 33 - - - 108128 RMVar_ID_108128 Human_SNP_ID_679849227 m1A Human chr20 + 35632922 35632922 35632922 TGGACAGCTGAACCAAGGTCACGCAGTGGGCCATCTGAGGGAAAAGGAGCTGGGTCAAGCACCAG TGGACAGCTGAACCAAGGTCACGCAGTGGGCCGTCTGAGGGAAAAGGAGCTGGGTCAAGCACCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:35632826..35632973;chr20:35632826..35632925;chr20:35632826..35655234 26863196 MeRIP-seq:(Medium) rs748081065 Functional Loss SNV dbSNP153 33..33 33 - - - 108129 RMVar_ID_108129 Human_SNP_ID_679849228 m1A Human chr20 - 35632925 35632924 35632925 TCCCTGGTGCTTGACCCAGCTCCTTTTCCCTCAGATGGCCCACTGCGTGACCTTGGTTCAGCTGT TCCCTGGTGCTTGACCCAGCTCCTTTTCCCTC_GATGGCCCACTGCGTGACCTTGGTTCAGCTGT CT C AL109827.1,CPNE1 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078 Protein coding,Protein coding intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:35632876..35632980 26863410 MeRIP-seq:(Medium) rs1172698731 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4662831,Human_RBP_ID_22549185 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727 108130 RMVar_ID_108130 Human_SNP_ID_679854586 m1A Human chr20 - 35653234 35653233 35653234 GACTGCCTGGTGCGGGAATGCCCAGTGCAGGAATACCTAGTGCAGGAGGTGAAGAGCATGCCTTC GACTGCCTGGTGCGGGAATGCCCAGTGCAGGA_TACCTAGTGCAGGAGGTGAAGAGCATGCCTTC AT A AL109827.1,CPNE1,RBM12 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078,Ensembl:ENSG00000244462 Protein coding,Protein coding,Protein coding intron,intron,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:35653143..35653243 32194978 MeRIP-seq:(Medium) rs763287249 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1025684,Human_RBP_ID_1595789,Human_RBP_ID_1928671,Human_RBP_ID_2682981,Human_RBP_ID_3647266,Human_RBP_ID_6995137,Human_RBP_ID_8854088,Human_RBP_ID_9297974,Human_RBP_ID_17970559,Human_RBP_ID_22722238 Human_miRNA_ID_208682 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727 108131 RMVar_ID_108131 Human_SNP_ID_679855053 m1A Human chr20 - 35654505 35654505 35654505 TGGAGCACCTATGAATTTGAACAATAATCTGAATCCTATGTTTCTTGGTCCGTTGAATCCTGTTA TGGAGCACCTATGAATTTGAACAATAATCTGAGTCCTATGTTTCTTGGTCCGTTGAATCCTGTTA T C AL109827.1,CPNE1,RBM12 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078,Ensembl:ENSG00000244462 Protein coding,Protein coding,Protein coding intron,intron,CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:35654503..35654658 26863196 MeRIP-seq:(Medium) rs1160418866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63330,Human_RBP_ID_1198108,Human_RBP_ID_1928694,Human_RBP_ID_2683014,Human_RBP_ID_3647275,Human_RBP_ID_8854126,Human_RBP_ID_14086452,Human_RBP_ID_17282933,Human_RBP_ID_20647798,Human_RBP_ID_23902256,Human_RBP_ID_27296169 Human_miRNA_ID_1433191,Human_miRNA_ID_2732307,Human_miRNA_ID_3104095 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727,RMVar_hsa_circ_111708,RMVar_hsa_circ_209733,RMVar_hsa_circ_209734 108132 RMVar_ID_108132 Human_SNP_ID_679856240 m1A Human chr20 - 35658955 35658955 35658955 CACAGGATTGACTTGGCCTCTACTTCTTGTTAAGGAAATTCATCTCTTGTTTTATCAGGTAAGAG CACAGGATTGACTTGGCCTCTACTTCTTGTTAGGGAAATTCATCTCTTGTTTTATCAGGTAAGAG T C AL109827.1,CPNE1,RBM12 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078,Ensembl:ENSG00000244462 Protein coding,Protein coding,Protein coding CDS,5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35658951..35659025 26863196 MeRIP-seq:(Medium) rs929967302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1928711,Human_RBP_ID_4644041,Human_RBP_ID_5147892,Human_RBP_ID_8942826,Human_RBP_ID_22817268,Human_RBP_ID_23902295,Human_RBP_ID_24560866,Human_RBP_ID_27296185 Human_Splice_Rec_2077086,Human_Splice_Rec_2077087,Human_Splice_Rec_2077446,Human_Splice_Rec_2077447,Human_Splice_Rec_2077460,Human_Splice_Rec_2077461,Human_Splice_Rec_2077486,Human_Splice_Rec_2077487,Human_Splice_Rec_2077496,Human_Splice_Rec_2077497,Human_Splice_Rec_2077508,Human_Splice_Rec_2077509,Human_Splice_Rec_2077524,Human_Splice_Rec_2077530,Human_Splice_Rec_2077531,Human_Splice_Rec_2077542,Human_Splice_Rec_2077543,Human_Splice_Rec_2077556,Human_Splice_Rec_2077557,Human_Splice_Rec_2077566,Human_Splice_Rec_2077567,Human_Splice_Rec_2077572,Human_Splice_Rec_2077573,Human_Splice_Rec_2077576,Human_Splice_Rec_2077577,Human_Splice_Rec_2077580,Human_Splice_Rec_2077581,Human_Splice_Rec_2077584,Human_Splice_Rec_2077585 Human_miRNA_ID_2066160,Human_miRNA_ID_2066161,Human_miRNA_ID_2935317,Human_miRNA_ID_2935318 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_336427,RMVar_hsa_circ_209727,RMVar_hsa_circ_111708,RMVar_hsa_circ_114560,RMVar_hsa_circ_209733,RMVar_hsa_circ_209734,RMVar_hsa_circ_285933,RMVar_hsa_circ_277647,RMVar_hsa_circ_209737,RMVar_hsa_circ_209738,RMVar_hsa_circ_209736 108133 RMVar_ID_108133 Human_SNP_ID_679857671 m1A Human chr20 + 35664860 35664860 35664860 GGCCGACAGCCCCAGCCCGAACGGCTTCCCGGAGCCCAACGCAGCCACCACCTCCTTCGCCGCTT GGCCGACAGCCCCAGCCCGAACGGCTTCCCGGGGCCCAACGCAGCCACCACCTCCTTCGCCGCTT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr20:35664711..35664875;chr20:35664524..35664925 26863410,26863196 MeRIP-seq:(Medium) rs1244144661 Functional Loss SNV dbSNP153 33..33 33 - - - 108134 RMVar_ID_108134 Human_SNP_ID_679860212 m1A Human chr20 - 35675017 35675017 35675017 TGGAGGTATGGGGAGAGCAGTTCCCTCCCACAACTTCTTCCCCTGTGCTGGGTCTCCTATTTAGA TGGAGGTATGGGGAGAGCAGTTCCCTCCCACAGCTTCTTCCCCTGTGCTGGGTCTCCTATTTAGA T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35675015..35675155 26863196 MeRIP-seq:(Medium) rs996733576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60187,RMVar_hsa_circ_352515 108135 RMVar_ID_108135 Human_SNP_ID_679860238 m1A Human chr20 + 35675095 35675095 35675095 CACCTCACACGCAGCCCCCAGCCCCACCACTAAGGGTGTGGGCACTGTCCCAGACCGCATACCCC CACCTCACACGCAGCCCCCAGCCCCACCACTACGGGTGTGGGCACTGTCCCAGACCGCATACCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35675010..35675225 26863196 MeRIP-seq:(Medium) rs1453693014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17970601 108136 RMVar_ID_108136 Human_SNP_ID_679861988 m1A Human chr20 - 35681979 35681979 35681979 TCTAGTCACCTTACTCCTGCATATCCCTAGGAACTAGAGGCTGCTATCCAGCCAGATACTAGCCT TCTAGTCACCTTACTCCTGCATATCCCTAGGAGCTAGAGGCTGCTATCCAGCCAGATACTAGCCT T C NFS1 Ensembl:ENSG00000244005 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:35681953..35682040 26863196 MeRIP-seq:(Medium) rs1317600442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19004139 Human_Splice_Rec_2077596,Human_Splice_Rec_2077597,Human_Splice_Rec_2077620,Human_Splice_Rec_2077621,Human_Splice_Rec_2077658,Human_Splice_Rec_2077659,Human_Splice_Rec_2077682,Human_Splice_Rec_2077683,Human_Splice_Rec_2077702,Human_Splice_Rec_2077703,Human_Splice_Rec_2077720,Human_Splice_Rec_2077721,Human_Splice_Rec_2077738 RMVar_hsa_circ_60187,RMVar_hsa_circ_352515,RMVar_hsa_circ_56155,RMVar_hsa_circ_317119,RMVar_hsa_circ_54298 108137 RMVar_ID_108137 Human_SNP_ID_679866364 m1A Human chr20 - 35698526 35698526 35698526 GCAGATACAGCCGCTGCCCCGGAGGTGGGGCCAGTGCTGCGACCTCTCTATATGGATGTGCAAGC GCAGATACAGCCGCTGCCCCGGAGGTGGGGCCGGTGCTGCGACCTCTCTATATGGATGTGCAAGC T C NFS1 Ensembl:ENSG00000244005 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35698441..35698624 26863196 MeRIP-seq:(Medium) rs370949785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659784,Human_RBP_ID_18771845,Human_RBP_ID_19005590 Human_Splice_Rec_2077588,Human_Splice_Rec_2077589,Human_Splice_Rec_2077612,Human_Splice_Rec_2077613,Human_Splice_Rec_2077650,Human_Splice_Rec_2077651,Human_Splice_Rec_2077674,Human_Splice_Rec_2077675,Human_Splice_Rec_2077696,Human_Splice_Rec_2077697,Human_Splice_Rec_2077728,Human_Splice_Rec_2077729,Human_Splice_Rec_2077740,Human_Splice_Rec_2077741,Human_Splice_Rec_2077749,Human_Splice_Rec_2077756,Human_Splice_Rec_2077757,Human_Splice_Rec_2077766,Human_Splice_Rec_2077767 Human_miRNA_ID_2156467,Human_miRNA_ID_2160027 RMVar_hsa_circ_15582,RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741 108138 RMVar_ID_108138 Human_SNP_ID_679866365 m1A Human chr20 - 35698526 35698526 35698526 GCAGATACAGCCGCTGCCCCGGAGGTGGGGCCAGTGCTGCGACCTCTCTATATGGATGTGCAAGC GCAGATACAGCCGCTGCCCCGGAGGTGGGGCCCGTGCTGCGACCTCTCTATATGGATGTGCAAGC T G NFS1 Ensembl:ENSG00000244005 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35698441..35698624 26863196 MeRIP-seq:(Medium) rs370949785 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_4659784,Human_RBP_ID_18771845,Human_RBP_ID_19005590 Human_Splice_Rec_2077588,Human_Splice_Rec_2077589,Human_Splice_Rec_2077612,Human_Splice_Rec_2077613,Human_Splice_Rec_2077650,Human_Splice_Rec_2077651,Human_Splice_Rec_2077674,Human_Splice_Rec_2077675,Human_Splice_Rec_2077696,Human_Splice_Rec_2077697,Human_Splice_Rec_2077728,Human_Splice_Rec_2077729,Human_Splice_Rec_2077740,Human_Splice_Rec_2077741,Human_Splice_Rec_2077749,Human_Splice_Rec_2077756,Human_Splice_Rec_2077757,Human_Splice_Rec_2077766,Human_Splice_Rec_2077767 Human_miRNA_ID_2156467,Human_miRNA_ID_2160027 RMVar_hsa_circ_15582,RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741 108139 RMVar_ID_108139 Human_SNP_ID_679866399 m1A Human chr20 + 35698577 35698577 35698577 GCGGCTGTATCTGCGGGAACCGCAGACTGAGGAGCACGGTCTCCAACTGATAAAAAATGGAACGG GCGGCTGTATCTGCGGGAACCGCAGACTGAGGTGCACGGTCTCCAACTGATAAAAAATGGAACGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35698435..35698634 26863196 MeRIP-seq:(Medium) rs774672929 Functional Loss SNV dbSNP153 33..33 33 - - - 108140 RMVar_ID_108140 Human_SNP_ID_679866619 m1A Human chr20 - 35699297 35699297 35699297 GACTGCAGCGGCTTCGGAAGGTGGGCTCTGCCAGCGGGACCATGCTGCTCCGAGCCGCTTGGAGG GACTGCAGCGGCTTCGGAAGGTGGGCTCTGCCTGCGGGACCATGCTGCTCCGAGCCGCTTGGAGG T A NFS1 Ensembl:ENSG00000244005 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:35699176..35699350;chr20:35699180..35699350;chr20:35699211..35699350 26863196 MeRIP-seq:(Medium) rs1006820376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659786,Human_RBP_ID_5503236,Human_RBP_ID_8942828,Human_RBP_ID_19005591 108141 RMVar_ID_108141 Human_SNP_ID_679866620 m1A Human chr20 - 35699297 35699297 35699297 GACTGCAGCGGCTTCGGAAGGTGGGCTCTGCCAGCGGGACCATGCTGCTCCGAGCCGCTTGGAGG GACTGCAGCGGCTTCGGAAGGTGGGCTCTGCCGGCGGGACCATGCTGCTCCGAGCCGCTTGGAGG T C NFS1 Ensembl:ENSG00000244005 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:35699176..35699350;chr20:35699180..35699350;chr20:35699211..35699350 26863196 MeRIP-seq:(Medium) rs1006820376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659786,Human_RBP_ID_5503236,Human_RBP_ID_8942828,Human_RBP_ID_19005591 108142 RMVar_ID_108142 Human_SNP_ID_679866688 m1A Human chr20 + 35699446 35699446 35699446 GAGAGACGTAGAGCTGAGCGACCCAGCCCGCGAGCGAGGTGAGGTAGGCGCCGGGCGACGCGGGG GAGAGACGTAGAGCTGAGCGACCCAGCCCGCGGGCGAGGTGAGGTAGGCGCCGGGCGACGCGGGG A G ROMO1 Ensembl:ENSG00000125995 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:35699426..35699564 26863196 MeRIP-seq:(Medium) rs1458476210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244451,Human_RBP_ID_779007,Human_RBP_ID_832315,Human_RBP_ID_4659366,Human_RBP_ID_18423321,Human_RBP_ID_18771847,Human_RBP_ID_22453473,Human_RBP_ID_23212445 Human_Splice_Rec_2077773,Human_Splice_Rec_2077777,Human_Splice_Rec_2077781,Human_Splice_Rec_2077785 RMVar_hsa_circ_107156,RMVar_hsa_circ_89517,RMVar_hsa_circ_209742,RMVar_hsa_circ_209743 108143 RMVar_ID_108143 Human_SNP_ID_679866763 m1A Human chr20 - 35699640 35699640 35699640 TTGGCTGGGACTGTCCGTAGGGACCCACGGCCACCGGCATCTGCGGGGGATAGGAAAGTGTGGGC TTGGCTGGGACTGTCCGTAGGGACCCACGGCCCCCGGCATCTGCGGGGGATAGGAAAGTGTGGGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35699626..35699675 26863196 MeRIP-seq:(Medium) rs764867344 Functional Loss SNV dbSNP153 33..33 33 - - - 108144 RMVar_ID_108144 Human_SNP_ID_679867147 m1A Human chr20 + 35700900 35700900 35700900 GGCACATTCATGGCCATTGGGATGGGCATCCGATGCTAACCATGGTTGCCAACTACATCTGTCCC GGCACATTCATGGCCATTGGGATGGGCATCCGTTGCTAACCATGGTTGCCAACTACATCTGTCCC A T ROMO1 Ensembl:ENSG00000125995 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35700761..35700900 26863196 MeRIP-seq:(Medium) rs1359736546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562835,Human_RBP_ID_8531890,Human_RBP_ID_17659038,Human_RBP_ID_22453478,Human_RBP_ID_23902374,Human_RBP_ID_26820805,Human_RBP_ID_27020177,Human_RBP_ID_27296204 Human_miRNA_ID_2133089 RMVar_hsa_circ_77090,RMVar_hsa_circ_107156,RMVar_hsa_circ_89517,RMVar_hsa_circ_209742,RMVar_hsa_circ_97828,RMVar_hsa_circ_209743,RMVar_hsa_circ_209744,RMVar_hsa_circ_209745 108145 RMVar_ID_108145 Human_SNP_ID_679867159 m1A Human chr20 + 35700938 35700938 35700938 ACCATGGTTGCCAACTACATCTGTCCCTTCCCATCAATCCCAGCCCATGTACTAATAAAAGAAAG ACCATGGTTGCCAACTACATCTGTCCCTTCCCGTCAATCCCAGCCCATGTACTAATAAAAGAAAG A G ROMO1 Ensembl:ENSG00000125995 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35700901..35701000 26863196 MeRIP-seq:(Medium) rs1285751909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562835,Human_RBP_ID_1380075,Human_RBP_ID_1595870,Human_RBP_ID_1928747,Human_RBP_ID_2683132,Human_RBP_ID_3647318,Human_RBP_ID_4662925,Human_RBP_ID_8531891,Human_RBP_ID_9116585,Human_RBP_ID_17658816,Human_RBP_ID_17970617,Human_RBP_ID_21895345,Human_RBP_ID_22452748,Human_RBP_ID_26489862,Human_RBP_ID_26670789,Human_RBP_ID_26820807 RMVar_hsa_circ_77090,RMVar_hsa_circ_107156,RMVar_hsa_circ_89517,RMVar_hsa_circ_209742,RMVar_hsa_circ_97828,RMVar_hsa_circ_209743,RMVar_hsa_circ_209744,RMVar_hsa_circ_209745 108146 RMVar_ID_108146 Human_SNP_ID_679870660 m1A Human chr20 - 35713269 35713269 35713269 TTGCCCAGGTTGGTCTCGATCTCTGGGATTTAAGTGAACCACCTCCCTTGGCCTCCCAGAGTGCT TTGCCCAGGTTGGTCTCGATCTCTGGGATTTAGGTGAACCACCTCCCTTGGCCTCCCAGAGTGCT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1436401929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3647377,Human_RBP_ID_6995689,Human_RBP_ID_14088124,Human_RBP_ID_17571570,Human_RBP_ID_18771907 RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_93394,RMVar_hsa_circ_209746,RMVar_hsa_circ_372199,RMVar_hsa_circ_209748,RMVar_hsa_circ_277732,RMVar_hsa_circ_112444,RMVar_hsa_circ_69232,RMVar_hsa_circ_209750,RMVar_hsa_circ_209751,RMVar_hsa_circ_73210,RMVar_hsa_circ_370386,RMVar_hsa_circ_50280,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_277461,RMVar_hsa_circ_61216,RMVar_hsa_circ_209754 108147 RMVar_ID_108147 Human_SNP_ID_679874320 m1A Human chr20 + 35724648 35724648 35724648 GTTAATCCTATTGCTAGAGGCACTGAGCTAACATCGACGAACTCCACATAAGCAATTCCTTTGGA GTTAATCCTATTGCTAGAGGCACTGAGCTAACGTCGACGAACTCCACATAAGCAATTCCTTTGGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:35724576..35724675 32194978 MeRIP-seq:(Medium) rs1218494108 Functional Loss SNV dbSNP153 33..33 33 - - - 108148 RMVar_ID_108148 Human_SNP_ID_679878899 m1A Human chr20 - 35738954 35738954 35738954 ATGAAGAACGTAGCAAAAAGTGAGTTTTAAGAAGGGGCTTGGGGGAGGGTGGTGAGCTTTTTTGT ATGAAGAACGTAGCAAAAAGTGAGTTTTAAGAGGGGGCTTGGGGGAGGGTGGTGAGCTTTTTTGT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:35738951..35739025;chr20:35738951..35739077 26863196 MeRIP-seq:(Medium) rs777033861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5089280,Human_RBP_ID_5383709,Human_RBP_ID_6996264,Human_RBP_ID_8532094,Human_RBP_ID_17618953,Human_RBP_ID_19106376 Human_Splice_Rec_2077794,Human_Splice_Rec_2077828,Human_Splice_Rec_2077864,Human_Splice_Rec_2077954,Human_Splice_Rec_2077986,Human_Splice_Rec_2078022,Human_Splice_Rec_2078054,Human_Splice_Rec_2078106,Human_Splice_Rec_2078140,Human_Splice_Rec_2078172,Human_Splice_Rec_2078328,Human_Splice_Rec_2078346,Human_Splice_Rec_2078362,Human_Splice_Rec_2078374,Human_Splice_Rec_2078396,Human_Splice_Rec_2078406,Human_Splice_Rec_2078414,Human_Splice_Rec_2078420,Human_Splice_Rec_2078428,Human_Splice_Rec_2078436,Human_Splice_Rec_2078452,Human_Splice_Rec_2078462,Human_Splice_Rec_2078468 RMVar_hsa_circ_24049,RMVar_hsa_circ_73210,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_14238,RMVar_hsa_circ_21028,RMVar_hsa_circ_209756,RMVar_hsa_circ_61575,RMVar_hsa_circ_328158,RMVar_hsa_circ_321303,RMVar_hsa_circ_209767,RMVar_hsa_circ_355610,RMVar_hsa_circ_42883,RMVar_hsa_circ_366360,RMVar_hsa_circ_353222 108149 RMVar_ID_108149 Human_SNP_ID_679878919 m1A Human chr20 + 35739015 35739015 35739015 TCATGGCCGTTGGCACTGCTCAACTTGTTCTCATCCTAAGCAGGGTTGATAGAAGAACATCATGA TCATGGCCGTTGGCACTGCTCAACTTGTTCTCGTCCTAAGCAGGGTTGATAGAAGAACATCATGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:35738976..35739077 32194978 MeRIP-seq:(Medium) rs752483626 Functional Loss SNV dbSNP153 33..33 33 - - - 108150 RMVar_ID_108150 Human_SNP_ID_679879925 m1A Human chr20 - 35742009 35742005 35742010 TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG TTAACAGTAGCAACAGAAGCGGCGGCGGCGG_____GCAGCAGCAGCAGCAGCAATCTCTTCCCG CTGCTG C RBM39 Ensembl:ENSG00000131051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35741891..35742262 26863196 MeRIP-seq:(Medium) rs1050876471 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_22257639,Human_RBP_ID_22817373,Human_RBP_ID_25627402,Human_RBP_ID_27020297 Human_Splice_Rec_2077791,Human_Splice_Rec_2077825,Human_Splice_Rec_2077859,Human_Splice_Rec_2077893,Human_Splice_Rec_2077951,Human_Splice_Rec_2077983,Human_Splice_Rec_2078017,Human_Splice_Rec_2078051,Human_Splice_Rec_2078103,Human_Splice_Rec_2078135,Human_Splice_Rec_2078169,Human_Splice_Rec_2078325,Human_Splice_Rec_2078341,Human_Splice_Rec_2078391,Human_Splice_Rec_2078417,Human_Splice_Rec_2078433,Human_Splice_Rec_2078447,Human_Splice_Rec_2078457,Human_Splice_Rec_2078465,Human_Splice_Rec_2078471,Human_Splice_Rec_2078477 RMVar_hsa_circ_47906,RMVar_hsa_circ_353222,RMVar_hsa_circ_61747 108151 RMVar_ID_108151 Human_SNP_ID_679879929 m1A Human chr20 - 35742009 35742008 35742009 TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG TTAACAGTAGCAACAGAAGCGGCGGCGGCGGC_GCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG CT C RBM39 Ensembl:ENSG00000131051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35741891..35742262 26863196 MeRIP-seq:(Medium) rs1406757463 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22257639,Human_RBP_ID_22817373,Human_RBP_ID_25627402,Human_RBP_ID_27020297 Human_Splice_Rec_2077791,Human_Splice_Rec_2077825,Human_Splice_Rec_2077859,Human_Splice_Rec_2077893,Human_Splice_Rec_2077951,Human_Splice_Rec_2077983,Human_Splice_Rec_2078017,Human_Splice_Rec_2078051,Human_Splice_Rec_2078103,Human_Splice_Rec_2078135,Human_Splice_Rec_2078169,Human_Splice_Rec_2078325,Human_Splice_Rec_2078341,Human_Splice_Rec_2078391,Human_Splice_Rec_2078417,Human_Splice_Rec_2078433,Human_Splice_Rec_2078447,Human_Splice_Rec_2078457,Human_Splice_Rec_2078465,Human_Splice_Rec_2078471,Human_Splice_Rec_2078477 RMVar_hsa_circ_47906,RMVar_hsa_circ_353222,RMVar_hsa_circ_61747 108152 RMVar_ID_108152 Human_SNP_ID_679879930 m1A Human chr20 - 35742009 35742009 35742009 TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG T C RBM39 Ensembl:ENSG00000131051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35741891..35742262 26863196 MeRIP-seq:(Medium) rs543109948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22257639,Human_RBP_ID_22817373,Human_RBP_ID_25627402,Human_RBP_ID_27020297 Human_Splice_Rec_2077791,Human_Splice_Rec_2077825,Human_Splice_Rec_2077859,Human_Splice_Rec_2077893,Human_Splice_Rec_2077951,Human_Splice_Rec_2077983,Human_Splice_Rec_2078017,Human_Splice_Rec_2078051,Human_Splice_Rec_2078103,Human_Splice_Rec_2078135,Human_Splice_Rec_2078169,Human_Splice_Rec_2078325,Human_Splice_Rec_2078341,Human_Splice_Rec_2078391,Human_Splice_Rec_2078417,Human_Splice_Rec_2078433,Human_Splice_Rec_2078447,Human_Splice_Rec_2078457,Human_Splice_Rec_2078465,Human_Splice_Rec_2078471,Human_Splice_Rec_2078477 RMVar_hsa_circ_47906,RMVar_hsa_circ_353222,RMVar_hsa_circ_61747 108153 RMVar_ID_108153 Human_SNP_ID_679879948 m1A Human chr20 - 35742047 35742047 35742047 ATTCGGGCTGGGCGGTTCCGCGGCCTGGGCCTAGGGGCTTAACAGTAGCAACAGAAGCGGCGGCG ATTCGGGCTGGGCGGTTCCGCGGCCTGGGCCTGGGGGCTTAACAGTAGCAACAGAAGCGGCGGCG T C RBM39 Ensembl:ENSG00000131051 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr20:35741902..35742250;chr20:35741926..35742150 26863196,32194978 MeRIP-seq:(Medium) rs1199950777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244871,Human_RBP_ID_779961,Human_RBP_ID_924866,Human_RBP_ID_1596223,Human_RBP_ID_1929031,Human_RBP_ID_4662955,Human_RBP_ID_5423666,Human_RBP_ID_5471808,Human_RBP_ID_6996342,Human_RBP_ID_8532128,Human_RBP_ID_14089795,Human_RBP_ID_18423287,Human_RBP_ID_18444296,Human_RBP_ID_18772096,Human_RBP_ID_23001760,Human_RBP_ID_23902615,Human_RBP_ID_25607633,Human_RBP_ID_27020298 Human_Splice_Rec_2077858 RMVar_hsa_circ_47906,RMVar_hsa_circ_353222,RMVar_hsa_circ_61747 108154 RMVar_ID_108154 Human_SNP_ID_679895536 m1A Human chr20 + 35801541 35801541 35801541 GTTGATGACTGAAAATGACAAAGCATCCACCTAACAGACGAGGAATCAGCTTTGAAGTGGGAGCC GTTGATGACTGAAAATGACAAAGCATCCACCTCACAGACGAGGAATCAGCTTTGAAGTGGGAGCC A C PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr20:35801476..35801625;chr20:35801444..35801564 26863196 MeRIP-seq:(Medium) rs778378425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61898,Human_RBP_ID_26342923 Human_Splice_Rec_2078494,Human_Splice_Rec_2078496,Human_Splice_Rec_2078497,Human_Splice_Rec_2078532,Human_Splice_Rec_2078533,Human_Splice_Rec_2078540,Human_Splice_Rec_2078541,Human_Splice_Rec_2078560,Human_Splice_Rec_2078561,Human_Splice_Rec_2078580,Human_Splice_Rec_2078581 Human_miRNA_ID_2407553,Human_miRNA_ID_2410548 RMVar_hsa_circ_70335,RMVar_hsa_circ_209777,RMVar_hsa_circ_326422,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_354161,RMVar_hsa_circ_361489,RMVar_hsa_circ_343297,RMVar_hsa_circ_60073,RMVar_hsa_circ_291760,RMVar_hsa_circ_54136,RMVar_hsa_circ_280018,RMVar_hsa_circ_299824,RMVar_hsa_circ_362973,RMVar_hsa_circ_365880,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_286782,RMVar_hsa_circ_299797,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_275412,RMVar_hsa_circ_105493,RMVar_hsa_circ_209781,RMVar_hsa_circ_209783,RMVar_hsa_circ_209784,RMVar_hsa_circ_209785,RMVar_hsa_circ_209782,RMVar_hsa_circ_209779,RMVar_hsa_circ_209780,RMVar_hsa_circ_209778 108155 RMVar_ID_108155 Human_SNP_ID_679901974 m1A Human chr20 + 35826428 35826428 35826428 CACATTTAGCTGTCTGGGTACAGGAATGGAGAATGTGGAGTCTGAAATAACCAGGGTTGGGTGGC CACATTTAGCTGTCTGGGTACAGGAATGGAGAGTGTGGAGTCTGAAATAACCAGGGTTGGGTGGC A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35826427..35826615 26863196 MeRIP-seq:(Medium) rs1286863921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14090358 RMVar_hsa_circ_70335,RMVar_hsa_circ_326422,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_354161,RMVar_hsa_circ_361489,RMVar_hsa_circ_343297,RMVar_hsa_circ_60073,RMVar_hsa_circ_54136,RMVar_hsa_circ_280018,RMVar_hsa_circ_299824,RMVar_hsa_circ_365880,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_286782,RMVar_hsa_circ_299797,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_275412,RMVar_hsa_circ_105493,RMVar_hsa_circ_209781,RMVar_hsa_circ_209783,RMVar_hsa_circ_209784,RMVar_hsa_circ_209785,RMVar_hsa_circ_209782,RMVar_hsa_circ_209779,RMVar_hsa_circ_209780,RMVar_hsa_circ_209778 108156 RMVar_ID_108156 Human_SNP_ID_679901975 m1A Human chr20 + 35826428 35826428 35826428 CACATTTAGCTGTCTGGGTACAGGAATGGAGAATGTGGAGTCTGAAATAACCAGGGTTGGGTGGC CACATTTAGCTGTCTGGGTACAGGAATGGAGATTGTGGAGTCTGAAATAACCAGGGTTGGGTGGC A T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35826427..35826615 26863196 MeRIP-seq:(Medium) rs1286863921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14090358 RMVar_hsa_circ_70335,RMVar_hsa_circ_326422,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_354161,RMVar_hsa_circ_361489,RMVar_hsa_circ_343297,RMVar_hsa_circ_60073,RMVar_hsa_circ_54136,RMVar_hsa_circ_280018,RMVar_hsa_circ_299824,RMVar_hsa_circ_365880,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_286782,RMVar_hsa_circ_299797,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_275412,RMVar_hsa_circ_105493,RMVar_hsa_circ_209781,RMVar_hsa_circ_209783,RMVar_hsa_circ_209784,RMVar_hsa_circ_209785,RMVar_hsa_circ_209782,RMVar_hsa_circ_209779,RMVar_hsa_circ_209780,RMVar_hsa_circ_209778 108157 RMVar_ID_108157 Human_SNP_ID_679909190 m1A Human chr20 + 35856875 35856875 35856875 TCACTTTGAGTTGGTGGGTATTGGATGGTGGTAATGGGAAATAAGGTTTGGAAAATTATTGGGGT TCACTTTGAGTTGGTGGGTATTGGATGGTGGTGATGGGAAATAAGGTTTGGAAAATTATTGGGGT A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35856869..35856984 26863196 MeRIP-seq:(Medium) rs1568659796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12929,RMVar_hsa_circ_70335,RMVar_hsa_circ_326422,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_354161,RMVar_hsa_circ_361489,RMVar_hsa_circ_60073,RMVar_hsa_circ_299824,RMVar_hsa_circ_365880,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_286782,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_275412,RMVar_hsa_circ_105493,RMVar_hsa_circ_127931,RMVar_hsa_circ_209781,RMVar_hsa_circ_209783,RMVar_hsa_circ_209784,RMVar_hsa_circ_209782,RMVar_hsa_circ_317863,RMVar_hsa_circ_348154,RMVar_hsa_circ_209779,RMVar_hsa_circ_209780,RMVar_hsa_circ_209778,RMVar_hsa_circ_365951,RMVar_hsa_circ_327908,RMVar_hsa_circ_343917,RMVar_hsa_circ_320927,RMVar_hsa_circ_279570,RMVar_hsa_circ_209788,RMVar_hsa_circ_209790,RMVar_hsa_circ_209792,RMVar_hsa_circ_209793,RMVar_hsa_circ_209791,RMVar_hsa_circ_209789,RMVar_hsa_circ_108966,RMVar_hsa_circ_284734,RMVar_hsa_circ_287406,RMVar_hsa_circ_311295,RMVar_hsa_circ_285004,RMVar_hsa_circ_116796,RMVar_hsa_circ_86993,RMVar_hsa_circ_209795,RMVar_hsa_circ_209797,RMVar_hsa_circ_209798,RMVar_hsa_circ_209799,RMVar_hsa_circ_209796,RMVar_hsa_circ_209794 108158 RMVar_ID_108158 Human_SNP_ID_679931761 m1A Human chr20 + 35954252 35954252 35954252 AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCAGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCGGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:35953626..35954565;chr20:35953965..35954500 26863196 MeRIP-seq:(Medium) rs955575094 Functional Loss SNV dbSNP153 33..33 33 - - - 108159 RMVar_ID_108159 Human_SNP_ID_679931762 m1A Human chr20 + 35954252 35954252 35954252 AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCAGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCTGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:35953626..35954565;chr20:35953965..35954500 26863196 MeRIP-seq:(Medium) rs955575094 Functional Loss SNV dbSNP153 33..33 33 - - - 108160 RMVar_ID_108160 Human_SNP_ID_679931771 m1A Human chr20 + 35954263 35954263 35954263 TGGCACCGCCGCGGGACTCCCAGTGGCCGCCAAGATCGGCTCCGTAGCCGCCATAACTCCAGCTC TGGCACCGCCGCGGGACTCCCAGTGGCCGCCACGATCGGCTCCGTAGCCGCCATAACTCCAGCTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35953709..35954500 26863196 MeRIP-seq:(Medium) rs1346601466 Functional Loss SNV dbSNP153 33..33 33 - - - 108161 RMVar_ID_108161 Human_SNP_ID_679932083 m1A Human chr20 - 35954805 35954805 35954805 ACCCTAATCATTCCCGAAGGAGGGGCCATCAGAGCTACAGCTCATCAGGGTCAATCAGAAGGGGC ACCCTAATCATTCCCGAAGGAGGGGCCATCAGGGCTACAGCTCATCAGGGTCAATCAGAAGGGGC T C SCAND1 Ensembl:ENSG00000171222 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35954662..35954814 26863196 MeRIP-seq:(Medium) rs1289968635 Functional Loss SNV dbSNP153 33..33 33 - - - 108162 RMVar_ID_108162 Human_SNP_ID_679954083 m1A Human chr20 + 36047128 36047128 36047128 AGTTCAAGCGATTCTCCTGCCTCAGCCTCTCGAGTAACTGGGGCTACAGGTGGGCACCACCACGA AGTTCAAGCGATTCTCCTGCCTCAGCCTCTCGTGTAACTGGGGCTACAGGTGGGCACCACCACGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36047003..36047193 26863196 MeRIP-seq:(Medium) rs1267311524 Functional Loss SNV dbSNP153 33..33 33 - - - 108163 RMVar_ID_108163 Human_SNP_ID_679954928 m1A Human chr20 + 36050606 36050606 36050606 GCTGCCGCCATACTTCCCGGCCCACCACGCCCAGCGCCGCCCAAAGGCGCTGCGTCCCGGCGGCT GCTGCCGCCATACTTCCCGGCCCACCACGCCCTGCGCCGCCCAAAGGCGCTGCGTCCCGGCGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:36050559..36050693 26863196 MeRIP-seq:(Medium) rs778245891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209822 108164 RMVar_ID_108164 Human_SNP_ID_679954975 m1A Human chr20 - 36050679 36050679 36050679 CCGTGGCGTCTCCCAGCCCGGACCCCGCCGGCACCCGGGTCTCCCGACCCAAGCCTCGACGAAAC CCGTGGCGTCTCCCAGCCCGGACCCCGCCGGCTCCCGGGTCTCCCGACCCAAGCCTCGACGAAAC T A NORAD Ensembl:ENSG00000260032 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:36050563..36050950 26863196 MeRIP-seq:(Medium) rs1357324083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244996,Human_RBP_ID_563106,Human_RBP_ID_3657123,Human_RBP_ID_4659376,Human_RBP_ID_5089331,Human_RBP_ID_5100541,Human_RBP_ID_5201640,Human_RBP_ID_5652708,Human_RBP_ID_9298472,Human_RBP_ID_21895378,Human_RBP_ID_26489958,Human_RBP_ID_27296329,Human_RBP_ID_27485099 Human_miRNA_ID_3209653 108165 RMVar_ID_108165 Human_SNP_ID_679955064 m1A Human chr20 + 36050900 36050900 36050900 TTCACCCGCCGGCCCGGGGCCGGAGGGCCTGGAGGGCCCTGGAGGAGCGGGCTGCGTTCTGCGTC TTCACCCGCCGGCCCGGGGCCGGAGGGCCTGGGGGGCCCTGGAGGAGCGGGCTGCGTTCTGCGTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:36050628..36050950 26863196 MeRIP-seq:(Medium) rs958571205 Functional Loss SNV dbSNP153 33..33 33 - - - 108166 RMVar_ID_108166 Human_SNP_ID_679955069 m1A Human chr20 - 36050907 36050907 36050907 GCGGAGAGACGCAGAACGCAGCCCGCTCCTCCAGGGCCCTCCAGGCCCTCCGGCCCCGGGCCGGC GCGGAGAGACGCAGAACGCAGCCCGCTCCTCCGGGGCCCTCCAGGCCCTCCGGCCCCGGGCCGGC T C NORAD Ensembl:ENSG00000260032 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:36050796..36050950 26863196 MeRIP-seq:(Medium) rs991722302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244990,Human_RBP_ID_779386,Human_RBP_ID_831383,Human_RBP_ID_926430,Human_RBP_ID_1601199,Human_RBP_ID_4644662,Human_RBP_ID_5100543,Human_RBP_ID_5323232,Human_RBP_ID_5503249,Human_RBP_ID_5596329,Human_RBP_ID_5652702,Human_RBP_ID_9116778,Human_RBP_ID_22453069,Human_RBP_ID_22533617 108167 RMVar_ID_108167 Human_SNP_ID_679955082 m1A Human chr20 - 36050927 36050927 36050927 GTTCCGGTCCGGCAGAGATCGCGGAGAGACGCAGAACGCAGCCCGCTCCTCCAGGGCCCTCCAGG GTTCCGGTCCGGCAGAGATCGCGGAGAGACGCGGAACGCAGCCCGCTCCTCCAGGGCCCTCCAGG T C NORAD Ensembl:ENSG00000260032 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36050901..36050950 26863196 MeRIP-seq:(Medium) rs943653377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244990,Human_RBP_ID_779386,Human_RBP_ID_1601199,Human_RBP_ID_3657124,Human_RBP_ID_4659804,Human_RBP_ID_5089333,Human_RBP_ID_5596329,Human_RBP_ID_9116778,Human_RBP_ID_22453069 108168 RMVar_ID_108168 Human_SNP_ID_679964743 m1A Human chr20 - 36091877 36091877 36091877 TACACACTGAGGCTAGGAGAGAGGAGGAACTAACCCGTGTTCAGCGAGCCCAAGATAGCATCTGA TACACACTGAGGCTAGGAGAGAGGAGGAACTACCCCGTGTTCAGCGAGCCCAAGATAGCATCTGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:36091868..36091969 26863196 MeRIP-seq:(Medium) rs1190124971 Functional Loss SNV dbSNP153 33..33 33 - - - 108169 RMVar_ID_108169 Human_SNP_ID_679967466 m1A Human chr20 - 36104141 36104141 36104141 CACATCTCTGCCAGACACTGACTTCTTGTACTAGAGTCTTACTGCCTCATTTGACCTTAAGACCC CACATCTCTGCCAGACACTGACTTCTTGTACTGGAGTCTTACTGCCTCATTTGACCTTAAGACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36104133..36104632 26863196 MeRIP-seq:(Medium) rs891342866 Functional Loss SNV dbSNP153 33..33 33 - - - 108170 RMVar_ID_108170 Human_SNP_ID_679967475 m1A Human chr20 + 36104194 36104194 36104194 GGCAGAGATGTGGCTGAGTGAGTTGAGGGGGGAGTCATTAGTGTAGAGGTGACAACAGGCTAGAG GGCAGAGATGTGGCTGAGTGAGTTGAGGGGGGCGTCATTAGTGTAGAGGTGACAACAGGCTAGAG A C EPB41L1 Ensembl:ENSG00000088367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:36104184..36104622 26863196 MeRIP-seq:(Medium) rs1376988543 Functional Loss SNV dbSNP153 33..33 33 - - - 108171 RMVar_ID_108171 Human_SNP_ID_679972254 m1A Human chr20 - 36125670 36125670 36125670 GTCAATATACACGGGCTGCAGGAGCTGGACCCACCTGCCACTCCACTTGCCTCCTTGCCGTCCCC GTCAATATACACGGGCTGCAGGAGCTGGACCCCCCTGCCACTCCACTTGCCTCCTTGCCGTCCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36125665..36126028 26863196 MeRIP-seq:(Medium) rs895476790 Functional Loss SNV dbSNP153 33..33 33 - - - 108172 RMVar_ID_108172 Human_SNP_ID_679978941 m1A Human chr20 - 36154737 36154728 36154737 GACACCCCCGCCCGCTGATGGATGCCGACTGCAGCAGCGGCGGCGGCGGCGGCGGCTCGGCGTGC GACACCCCCGCCCGCTGATGGATGCCGACTGC_________GGCGGCGGCGGCGGCTCGGCGTGC CGCCGCTGCT C AL121895.1 Ensembl:ENSG00000232406 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36154725..36154900 26863196 MeRIP-seq:(Medium) rs1294507983 Functional Loss DEL dbSNP153 33..41 33 - - - 108173 RMVar_ID_108173 Human_SNP_ID_679978943 m1A Human chr20 - 36154734 36154734 36154734 ACCCCCGCCCGCTGATGGATGCCGACTGCAGCAGCGGCGGCGGCGGCGGCGGCTCGGCGTGCGCC ACCCCCGCCCGCTGATGGATGCCGACTGCAGCGGCGGCGGCGGCGGCGGCGGCTCGGCGTGCGCC T C AL121895.1 Ensembl:ENSG00000232406 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:36154642..36154875;chr20:36154722..36154921;chr20:36154728..36154931 26863410,26863196,26863196 MeRIP-seq:(Medium) rs1367119667 Functional Loss SNV dbSNP153 33..33 33 - - - 108174 RMVar_ID_108174 Human_SNP_ID_679978944 m1A Human chr20 - 36154737 36154737 36154737 GACACCCCCGCCCGCTGATGGATGCCGACTGCAGCAGCGGCGGCGGCGGCGGCGGCTCGGCGTGC GACACCCCCGCCCGCTGATGGATGCCGACTGCGGCAGCGGCGGCGGCGGCGGCGGCTCGGCGTGC T C AL121895.1 Ensembl:ENSG00000232406 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36154725..36154900 26863196 MeRIP-seq:(Medium) rs1015371146 Functional Loss SNV dbSNP153 33..33 33 - - - 108175 RMVar_ID_108175 Human_SNP_ID_679978963 m1A Human chr20 + 36154802 36154802 36154802 GCCGAACAGGCTGCTCCGCAGAGCCCGCCGCGACCCCGCGCCGCCCCGCCCCGCGGCCTGCCTGC GCCGAACAGGCTGCTCCGCAGAGCCCGCCGCGCCCCCGCGCCGCCCCGCCCCGCGGCCTGCCTGC A C EPB41L1 Ensembl:ENSG00000088367 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:36154798..36154886 26863196 MeRIP-seq:(Medium) rs967450288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4660375,Human_RBP_ID_9390566 Human_Splice_Rec_2079031,Human_Splice_Rec_2079073,Human_Splice_Rec_2079121 RMVar_hsa_circ_82936,RMVar_hsa_circ_39162,RMVar_hsa_circ_79103,RMVar_hsa_circ_209824,RMVar_hsa_circ_209825 108176 RMVar_ID_108176 Human_SNP_ID_679983549 m1A Human chr20 - 36175504 36175504 36175504 AAGGGAATAGTTTGCTCAGTGAGTTTTAAGCCATGGCCTTTCATATAAGTAAGAAGCAATATAGA AAGGGAATAGTTTGCTCAGTGAGTTTTAAGCCGTGGCCTTTCATATAAGTAAGAAGCAATATAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36175500..36175658 26863196 MeRIP-seq:(Medium) rs374593631 Functional Loss SNV dbSNP153 33..33 33 - - - 108177 RMVar_ID_108177 Human_SNP_ID_679987860 m1A Human chr20 + 36194331 36194331 36194331 GGCAACGGTCAGAGGCTGAGGAGGGAGAGGTCAGGACTCCAACCAAGATCAAGGAGCTAAAGGTA GGCAACGGTCAGAGGCTGAGGAGGGAGAGGTCGGGACTCCAACCAAGATCAAGGAGCTAAAGGTA A G EPB41L1 Ensembl:ENSG00000088367 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:36194201..36194391;chr20:36194178..36194389;chr20:36194229..36194396 26863196 MeRIP-seq:(Medium) rs753699939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778564,Human_RBP_ID_925678,Human_RBP_ID_5385063,Human_RBP_ID_19005637 Human_Splice_Rec_2078799,Human_Splice_Rec_2078865,Human_Splice_Rec_2078905,Human_Splice_Rec_2078945,Human_Splice_Rec_2078989,Human_Splice_Rec_2079053,Human_Splice_Rec_2079095,Human_Splice_Rec_2079151,Human_Splice_Rec_2079173 RMVar_hsa_circ_98747,RMVar_hsa_circ_39162,RMVar_hsa_circ_19213,RMVar_hsa_circ_209828,RMVar_hsa_circ_53043,RMVar_hsa_circ_42915,RMVar_hsa_circ_265108,RMVar_hsa_circ_209833 108178 RMVar_ID_108178 Human_SNP_ID_679988608 m1A Human chr20 + 36197929 36197929 36197929 GGCCAGCATCAATGAGCTCAAAAGGACCCTGAAGGAGCCCAACAGCAAACTCATCCACCGGGATC GGCCAGCATCAATGAGCTCAAAAGGACCCTGAGGGAGCCCAACAGCAAACTCATCCACCGGGATC A G EPB41L1 Ensembl:ENSG00000088367 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36197824..36197993 26863196 MeRIP-seq:(Medium) rs1384079427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2078800,Human_Splice_Rec_2078866,Human_Splice_Rec_2078906,Human_Splice_Rec_2078948,Human_Splice_Rec_2078990,Human_Splice_Rec_2079056,Human_Splice_Rec_2079098,Human_Splice_Rec_2079154,Human_Splice_Rec_2079174 RMVar_hsa_circ_98747,RMVar_hsa_circ_39162,RMVar_hsa_circ_19213,RMVar_hsa_circ_209828,RMVar_hsa_circ_42915,RMVar_hsa_circ_265108 108179 RMVar_ID_108179 Human_SNP_ID_679995766 m1A Human chr20 + 36230083 36230082 36230083 TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCCACCCCACACCCTTCACCCTCTGTGTCCTGGTCC TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCC_CCCCACACCCTTCACCCTCTGTGTCCTGGTCC CA C EPB41L1 Ensembl:ENSG00000088367 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36230032..36230150 26863196 MeRIP-seq:(Medium) rs1260405254 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_778566,Human_RBP_ID_17086763,Human_RBP_ID_17572167,Human_RBP_ID_17659337,Human_RBP_ID_18950530 Human_miRNA_ID_1704520,Human_miRNA_ID_2946417 RMVar_hsa_circ_98747,RMVar_hsa_circ_209828,RMVar_hsa_circ_124883,RMVar_hsa_circ_209834 108180 RMVar_ID_108180 Human_SNP_ID_679995768 m1A Human chr20 + 36230083 36230083 36230083 TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCCACCCCACACCCTTCACCCTCTGTGTCCTGGTCC TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCCCCCCCACACCCTTCACCCTCTGTGTCCTGGTCC A C EPB41L1 Ensembl:ENSG00000088367 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36230032..36230150 26863196 MeRIP-seq:(Medium) rs926201306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778566,Human_RBP_ID_17086763,Human_RBP_ID_17572167,Human_RBP_ID_17659337,Human_RBP_ID_18950530 Human_miRNA_ID_1704520,Human_miRNA_ID_2946417 RMVar_hsa_circ_98747,RMVar_hsa_circ_209828,RMVar_hsa_circ_124883,RMVar_hsa_circ_209834 108181 RMVar_ID_108181 Human_SNP_ID_680001564 m1A Human chr20 + 36255744 36255744 36255744 GGTGGAGCTCCCTGAGGGCATCGAGATGGGCTAACTCGGGGAGCGCTCTCAGCTGCGAGGGGCCC GGTGGAGCTCCCTGAGGGCATCGAGATGGGCTCACTCGGGGAGCGCTCTCAGCTGCGAGGGGCCC A C AAR2 Ensembl:ENSG00000131043 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36255694..36255843 32194978 MeRIP-seq:(Medium) rs370822975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4644791,Human_RBP_ID_6996877 RMVar_hsa_circ_108094,RMVar_hsa_circ_115622,RMVar_hsa_circ_209839,RMVar_hsa_circ_79059,RMVar_hsa_circ_98688,RMVar_hsa_circ_209840,RMVar_hsa_circ_209841,RMVar_hsa_circ_116508,RMVar_hsa_circ_209845,RMVar_hsa_circ_209846 108182 RMVar_ID_108182 Human_SNP_ID_680013535 m1A Human chr20 - 36306281 36306281 36306281 CTCCCCGAGAGCGGCGGGGAGGGGGCGGGGAGAGGGGAGAGGAGCGCGGGGGAGGGGGCCGTGCG CTCCCCGAGAGCGGCGGGGAGGGGGCGGGGAGGGGGGAGAGGAGCGCGGGGGAGGGGGCCGTGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:36306269..36306354 26863410 MeRIP-seq:(Medium) rs1345153966 Functional Loss SNV dbSNP153 33..33 33 - - - 108183 RMVar_ID_108183 Human_SNP_ID_680050311 m1A Human chr20 + 36461614 36461614 36461614 GCCTCCTCAGCCCGGACGCCCGGGGCCCGCCCAGCGCCGCCCGGAGCAGCCGCGGCCCCGCGAGG GCCTCCTCAGCCCGGACGCCCGGGGCCCGCCCCGCGCCGCCCGGAGCAGCCGCGGCCCCGCGAGG A C DLGAP4 Ensembl:ENSG00000080845 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:36461476..36461846 26863410 MeRIP-seq:(Medium) rs1483597143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9390570,Human_RBP_ID_18422876,Human_RBP_ID_26788368 RMVar_hsa_circ_95927,RMVar_hsa_circ_209851 108184 RMVar_ID_108184 Human_SNP_ID_680050391 m1A Human chr20 - 36461736 36461724 36461736 GCGGGCGGGCGGGCGGGCGGACGGACGGACGGACGGACAGACGGGGAGGAGGAGGAGGAGGAGGA GCGGGCGGGCGGGCGGGCGGACGGACGGACGG____________GGAGGAGGAGGAGGAGGAGGA CCCGTCTGTCCGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:36461570..36461749 26863196 MeRIP-seq:(Medium) rs1202419744 Functional Loss DEL dbSNP153 33..44 33 - - - 108185 RMVar_ID_108185 Human_SNP_ID_680050408 m1A Human chr20 - 36461736 36461736 36461736 GCGGGCGGGCGGGCGGGCGGACGGACGGACGGACGGACAGACGGGGAGGAGGAGGAGGAGGAGGA GCGGGCGGGCGGGCGGGCGGACGGACGGACGGGCGGACAGACGGGGAGGAGGAGGAGGAGGAGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:36461570..36461749 26863196 MeRIP-seq:(Medium) rs1179392547 Functional Loss SNV dbSNP153 33..33 33 - - - 108186 RMVar_ID_108186 Human_SNP_ID_680050501 m1A Human chr20 - 36461849 36461845 36461849 CTGCGGAGGAGCGCGAGGGCAGAGACAAAGAGACAGCGAGCCGGGGAGAGACAAAGCGGGCGGAG CTGCGGAGGAGCGCGAGGGCAGAGACAAAGAG____CGAGCCGGGGAGAGACAAAGCGGGCGGAG GCTGT G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:36461751..36462057 26863196 MeRIP-seq:(Medium) rs1199287178 Functional Loss DEL dbSNP153 33..36 33 - - - 108187 RMVar_ID_108187 Human_SNP_ID_680050503 m1A Human chr20 - 36461847 36461847 36461847 GCGGAGGAGCGCGAGGGCAGAGACAAAGAGACAGCGAGCCGGGGAGAGACAAAGCGGGCGGAGCG GCGGAGGAGCGCGAGGGCAGAGACAAAGAGACTGCGAGCCGGGGAGAGACAAAGCGGGCGGAGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36461476..36462000 26863196 MeRIP-seq:(Medium) rs1569506815 Functional Loss SNV dbSNP153 33..33 33 - - - 108188 RMVar_ID_108188 Human_SNP_ID_680050649 m1A Human chr20 - 36462336 36462336 36462336 GTGGGGGCACAGAGGGGCAGGGAGAGCAAAGCAGGGGACCCCGATCCCGAGAAGTGGGGGTGCTC GTGGGGGCACAGAGGGGCAGGGAGAGCAAAGCTGGGGACCCCGATCCCGAGAAGTGGGGGTGCTC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36462287..36462438 32194978 MeRIP-seq:(Medium) rs1307581360 Functional Loss SNV dbSNP153 33..33 33 - - - 108189 RMVar_ID_108189 Human_SNP_ID_680050662 m1A Human chr20 - 36462383 36462382 36462384 GGCCTTCAGCGCAAGAGGCACAGAGTGGCGAGACCACCGAGACAGATGTGGGGGCACAGAGGGGC GGCCTTCAGCGCAAGAGGCACAGAGTGGCGA__CCACCGAGACAGATGTGGGGGCACAGAGGGGC GTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36462244..36462490 26863196 MeRIP-seq:(Medium) rs1445776831 Functional Loss DEL dbSNP153 32..33 33 - - - 108190 RMVar_ID_108190 Human_SNP_ID_680056679 m1A Human chr20 + 36487151 36487151 36487151 GAGGAGGGTGGAAGGAGGAGATGGGAATTTCCATGCTTCTGGAGTGTATAACTGAGTGTTCAGGG GAGGAGGGTGGAAGGAGGAGATGGGAATTTCCGTGCTTCTGGAGTGTATAACTGAGTGTTCAGGG A G DLGAP4 Ensembl:ENSG00000080845 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:36487030..36487224 26863196 MeRIP-seq:(Medium) rs1004450986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17193005 RMVar_hsa_circ_95927,RMVar_hsa_circ_209851,RMVar_hsa_circ_209853 108191 RMVar_ID_108191 Human_SNP_ID_680063793 m1A Human chr20 - 36514889 36514889 36514889 CACCTCTCCTCAGACATGGCCTTTCTCCTGTCACTGTGGAGAAGCTATCTGTTCTCTACTTGGGC CACCTCTCCTCAGACATGGCCTTTCTCCTGTCGCTGTGGAGAAGCTATCTGTTCTCTACTTGGGC T C DLGAP4-AS1 Ensembl:ENSG00000232907 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:36514879..36515032 26863196 MeRIP-seq:(Medium) rs369715707 Functional Loss SNV dbSNP153 33..33 33 - - - 108192 RMVar_ID_108192 Human_SNP_ID_680073218 m1A Human chr20 + 36549188 36549188 36549188 GTACCGGGAGGCACCCATTGATAAGAAAGGCAACTTCAACTACGTGGAGTTCACCCGCATCCTCA GTACCGGGAGGCACCCATTGATAAGAAAGGCAGCTTCAACTACGTGGAGTTCACCCGCATCCTCA A G MYL9 Ensembl:ENSG00000101335 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:36549138..36549275 26863196 MeRIP-seq:(Medium) rs200473571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_83639,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_111388,RMVar_hsa_circ_209860,RMVar_hsa_circ_209861,RMVar_hsa_circ_209862 108193 RMVar_ID_108193 Human_SNP_ID_680073250 m1A Human chr20 + 36549258 36549258 36549258 GGCGCCAAGGATAAAGACGACTAGGCCACCCCAGCCCCCTGACACCCCAGCCCCCGCCAGTCACC GGCGCCAAGGATAAAGACGACTAGGCCACCCCCGCCCCCTGACACCCCAGCCCCCGCCAGTCACC A C MYL9 Ensembl:ENSG00000101335 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36549208..36549431 26863196 MeRIP-seq:(Medium) rs1014362532 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_2686440,Human_miRNA_ID_2686441 RMVar_hsa_circ_78663,RMVar_hsa_circ_83639,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_111388,RMVar_hsa_circ_209860,RMVar_hsa_circ_209861,RMVar_hsa_circ_209862 108194 RMVar_ID_108194 Human_SNP_ID_680079351 m1A Human chr20 + 36573651 36573651 36573651 CGCGAGCTGTCAGGCCGAGTGTCAGGCCGGGCAGGTACGCGGCGCGCGCCCCCGGCGCCCCCCGC CGCGAGCTGTCAGGCCGAGTGTCAGGCCGGGCGGGTACGCGGCGCGCGCCCCCGGCGCCCCCCGC A G TGIF2 Ensembl:ENSG00000118707 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:36573604..36574038;chr20:36573613..36574061;chr20:36573601..36573699 26863196 MeRIP-seq:(Medium) rs1279238853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659383,Human_RBP_ID_9331504,Human_RBP_ID_18444314,Human_RBP_ID_22081334,Human_RBP_ID_22453493 Human_Splice_Rec_2079471,Human_Splice_Rec_2079475,Human_Splice_Rec_2079479 RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_108964,RMVar_hsa_circ_209863,RMVar_hsa_circ_209864,RMVar_hsa_circ_209865 108195 RMVar_ID_108195 Human_SNP_ID_680079387 m1A Human chr20 + 36573745 36573745 36573745 GAGGCCGCGTGGACCCGAAAGCCGCTGGGAAAAGTCAGTGCAGGGAGCAGCAGAGGGCCAGATGG GAGGCCGCGTGGACCCGAAAGCCGCTGGGAAATGTCAGTGCAGGGAGCAGCAGAGGGCCAGATGG A T TGIF2 Ensembl:ENSG00000118707 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36573642..36573821 32194978 MeRIP-seq:(Medium) rs1230234917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659808 Human_Splice_Rec_2079475,Human_Splice_Rec_2079479 RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_108964,RMVar_hsa_circ_209863,RMVar_hsa_circ_209864,RMVar_hsa_circ_209865 108196 RMVar_ID_108196 Human_SNP_ID_680079415 m1A Human chr20 - 36573845 36573845 36573845 CCCGAGCTCACACACCCCCTACCGCACGCGCCAGGACGACGCCCCCTCCCCGTCCGGCCGAGAAA CCCGAGCTCACACACCCCCTACCGCACGCGCCGGGACGACGCCCCCTCCCCGTCCGGCCGAGAAA T C lnc-SLA2-1,lnc-SLA2-1:2 RNACentral:URS0000413E6C,RNACentral:URS0000D5BD1C lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:36573815..36574009 26863196 MeRIP-seq:(Medium) rs920666516 Functional Loss SNV dbSNP153 33..33 33 - - - 108197 RMVar_ID_108197 Human_SNP_ID_680087877 m1A Human chr20 + 36605826 36605826 36605826 CCGGGTAGCTTGGCCAGGTTGTGAGGAACCGCAGCGCGCCGCAGGACCGGGCCGCTGAGCCTGCA CCGGGTAGCTTGGCCAGGTTGTGAGGAACCGCGGCGCGCCGCAGGACCGGGCCGCTGAGCCTGCA A G RAB5IF,TGIF2-RAB5IF Ensembl:ENSG00000101084,Ensembl:ENSG00000259399 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:36605776..36606075 26863196 MeRIP-seq:(Medium) rs1185595537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616,Human_RBP_ID_244113,Human_RBP_ID_778627,Human_RBP_ID_831656,Human_RBP_ID_926778,Human_RBP_ID_1596359,Human_RBP_ID_4645042,Human_RBP_ID_5322929,Human_RBP_ID_9389148,Human_RBP_ID_17659048,Human_RBP_ID_18422878,Human_RBP_ID_22080643,Human_RBP_ID_22453072 RMVar_hsa_circ_87911,RMVar_hsa_circ_209866,RMVar_hsa_circ_209868,RMVar_hsa_circ_109383,RMVar_hsa_circ_268300 108198 RMVar_ID_108198 Human_SNP_ID_680087882 m1A Human chr20 + 36605839 36605839 36605839 CCAGGTTGTGAGGAACCGCAGCGCGCCGCAGGACCGGGCCGCTGAGCCTGCAGCCGCCCCGCGCC CCAGGTTGTGAGGAACCGCAGCGCGCCGCAGGGCCGGGCCGCTGAGCCTGCAGCCGCCCCGCGCC A G RAB5IF,TGIF2-RAB5IF Ensembl:ENSG00000101084,Ensembl:ENSG00000259399 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:36605776..36607750 26863196 MeRIP-seq:(Medium) rs1282807320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616,Human_RBP_ID_244113,Human_RBP_ID_778627,Human_RBP_ID_831656,Human_RBP_ID_926778,Human_RBP_ID_1596360,Human_RBP_ID_4645046,Human_RBP_ID_5322929,Human_RBP_ID_5471827,Human_RBP_ID_8532333,Human_RBP_ID_9389148,Human_RBP_ID_17659048,Human_RBP_ID_22080643,Human_RBP_ID_22453072 Human_miRNA_ID_2270637 RMVar_hsa_circ_87911,RMVar_hsa_circ_209866,RMVar_hsa_circ_209868,RMVar_hsa_circ_109383,RMVar_hsa_circ_268300 108199 RMVar_ID_108199 Human_SNP_ID_680110928 m1A Human chr20 + 36695781 36695763 36695782 CTAGTTTCGCCCTGGCCTTGTGACCTTGCCCTACCCTTGTGACCTTGCCCTATCCATTTGCCTTG CTAGTTTCGCCCTGG___________________CCTTGTGACCTTGCCCTATCCATTTGCCTTG GCCTTGTGACCTTGCCCTAC G RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36695761..36695915 26863196 MeRIP-seq:(Medium) rs1247361128 Functional Loss DEL dbSNP153 16..34 33 - - - 108200 RMVar_ID_108200 Human_SNP_ID_680117278 m1A Human chr20 + 36721777 36721777 36721777 TAACGAGAGTAGAGGAATCTCAAGAATAAATCAGTAACTCTGAAACAGAAAAGAAAGAAGTGAAG TAACGAGAGTAGAGGAATCTCAAGAATAAATCGGTAACTCTGAAACAGAAAAGAAAGAAGTGAAG A G RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36721726..36721818 26863196 MeRIP-seq:(Medium) rs766927125 Functional Loss SNV dbSNP153 33..33 33 - - - 108201 RMVar_ID_108201 Human_SNP_ID_680130068 m1A Human chr20 - 36772212 36772212 36772212 AGAGACTATTAAGATAGTGGGAGGGACCAGAAATTATGAGACCTGAACTAAACTAGTAACAGTGA AGAGACTATTAAGATAGTGGGAGGGACCAGAAGTTATGAGACCTGAACTAAACTAGTAACAGTGA T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:36772209..36772325 26863196 MeRIP-seq:(Medium) rs1299328790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10017224,Human_RBP_ID_14093002,Human_RBP_ID_23001825,Human_RBP_ID_23284473 108202 RMVar_ID_108202 Human_SNP_ID_680130075 m1A Human chr20 - 36772249 36772249 36772249 ACTGGAGACGGGCCGTTGGAGGTAGAAAAACTAGTGGAGAGACTATTAAGATAGTGGGAGGGACC ACTGGAGACGGGCCGTTGGAGGTAGAAAAACTTGTGGAGAGACTATTAAGATAGTGGGAGGGACC T A DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36772244..36772327 26863196 MeRIP-seq:(Medium) rs796557108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1198209,Human_RBP_ID_10027581,Human_RBP_ID_14093002,Human_RBP_ID_23001826,Human_RBP_ID_25608773 108203 RMVar_ID_108203 Human_SNP_ID_680130175 m1A Human chr20 + 36772603 36772603 36772603 TGAGCCACCACACCCGGCCCAGTCTATTCTTCAGACAGTTGCCGGGACTTTTCCAAAGTGTAGTC TGAGCCACCACACCCGGCCCAGTCTATTCTTCGGACAGTTGCCGGGACTTTTCCAAAGTGTAGTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36772601..36772757 26863196 MeRIP-seq:(Medium) rs941282332 Functional Loss SNV dbSNP153 33..33 33 - - - 108204 RMVar_ID_108204 Human_SNP_ID_680130364 m1A Human chr20 - 36773470 36773470 36773470 GGGCGCTGCGACCTCCTCCCGGGTGAAATGAAACCCGAGGGCAGTCCCCCTTACCGACCCCATTA GGGCGCTGCGACCTCCTCCCGGGTGAAATGAAGCCCGAGGGCAGTCCCCCTTACCGACCCCATTA T C DSN1 Ensembl:ENSG00000149636 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36773419..36773718 32194978 MeRIP-seq:(Medium) rs112136831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563355,Human_RBP_ID_1596434,Human_RBP_ID_23903235 Human_Splice_Rec_2079709,Human_Splice_Rec_2079843,Human_Splice_Rec_2079865 108205 RMVar_ID_108205 Human_SNP_ID_680131401 m1A Human chr20 + 36777668 36777668 36777668 ATAGTGGACAAGAGAGGTGGACAGTTGGCCCAAGGATGCCCTTGGTCCCTTCCCTCCCATGGGCC ATAGTGGACAAGAGAGGTGGACAGTTGGCCCACGGATGCCCTTGGTCCCTTCCCTCCCATGGGCC A C NONHSAG031712.2 RNACentral:URS00008B5F16 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:36777626..36777769 26863196 MeRIP-seq:(Medium) rs182739151 Functional Loss SNV dbSNP153 33..33 33 - - - 108206 RMVar_ID_108206 Human_SNP_ID_680131448 m1A Human chr20 + 36777823 36777823 36777823 GCTGGGGAGGGGCCAGGATGAGGAGGAAGGGCAGCTTCTGGCTCTCTTCCCAGCTGCTGGGGGTT GCTGGGGAGGGGCCAGGATGAGGAGGAAGGGCGGCTTCTGGCTCTCTTCCCAGCTGCTGGGGGTT A G NONHSAG031712.2 RNACentral:URS00008B5F16 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36777773..36777930 26863196 MeRIP-seq:(Medium) rs1435796649 Functional Loss SNV dbSNP153 33..33 33 - - - 108207 RMVar_ID_108207 Human_SNP_ID_680133092 m1A Human chr20 - 36785752 36785752 36785752 GTTGGGGAGTGATTGCAATTGCCTTCCTTGCCAAAGTGACTTGGGGCCCCAACGTTCCCAGCAGA GTTGGGGAGTGATTGCAATTGCCTTCCTTGCCGAAGTGACTTGGGGCCCCAACGTTCCCAGCAGA T C SOGA1 Ensembl:ENSG00000149639 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36785629..36785929 32194978 MeRIP-seq:(Medium) rs1310388716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22081043,Human_RBP_ID_27296509 Human_miRNA_ID_139977,Human_miRNA_ID_416926,Human_miRNA_ID_2133095,Human_miRNA_ID_2249678,Human_miRNA_ID_2296469 RMVar_hsa_circ_209895,RMVar_hsa_circ_88558,RMVar_hsa_circ_91284,RMVar_hsa_circ_108748,RMVar_hsa_circ_78332,RMVar_hsa_circ_209896,RMVar_hsa_circ_209893,RMVar_hsa_circ_209894,RMVar_hsa_circ_209897,RMVar_hsa_circ_92322 108208 RMVar_ID_108208 Human_SNP_ID_680133208 m1A Human chr20 - 36786328 36786328 36786328 CAGTGATGCCACTGCCAGAATGCAGCTTTCACATCAAGGTAAAGCCGGGTCTCCTGCTGGCCCCT CAGTGATGCCACTGCCAGAATGCAGCTTTCACGTCAAGGTAAAGCCGGGTCTCCTGCTGGCCCCT T C SOGA1 Ensembl:ENSG00000149639 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36786278..36793938 32194978 MeRIP-seq:(Medium) rs949780651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4645370,Human_RBP_ID_8532429,Human_RBP_ID_22081044 RMVar_hsa_circ_209895,RMVar_hsa_circ_88558,RMVar_hsa_circ_91284,RMVar_hsa_circ_108748,RMVar_hsa_circ_78332,RMVar_hsa_circ_209896,RMVar_hsa_circ_209893,RMVar_hsa_circ_209894,RMVar_hsa_circ_209897,RMVar_hsa_circ_92322 108209 RMVar_ID_108209 Human_SNP_ID_680141054 m1A Human chr20 - 36815877 36815877 36815877 GCTGCGGCGACACCTGCAGTTTGTCGAAGAGGAGGCCGAGCTGCTGCGGCGCTCCTCTGCCGAGC GCTGCGGCGACACCTGCAGTTTGTCGAAGAGGGGGCCGAGCTGCTGCGGCGCTCCTCTGCCGAGC T C SOGA1 Ensembl:ENSG00000149639 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:36815826..36816100 26863196 MeRIP-seq:(Medium) rs1476155457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924492,Human_RBP_ID_5529072,Human_RBP_ID_9389156 RMVar_hsa_circ_108748,RMVar_hsa_circ_209896,RMVar_hsa_circ_290074,RMVar_hsa_circ_43114,RMVar_hsa_circ_209899,RMVar_hsa_circ_266929,RMVar_hsa_circ_83836,RMVar_hsa_circ_126199,RMVar_hsa_circ_348377,RMVar_hsa_circ_209903,RMVar_hsa_circ_209906,RMVar_hsa_circ_3935,RMVar_hsa_circ_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_378056,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209909 108210 RMVar_ID_108210 Human_SNP_ID_680141098 m1A Human chr20 - 36815987 36815987 36815987 CGGGCTGAGATGGACGACATGAAGGATCATGGAGGTGGCTGTGGGGGTCCTGAGGCACGCCTGGC CGGGCTGAGATGGACGACATGAAGGATCATGGGGGTGGCTGTGGGGGTCCTGAGGCACGCCTGGC T C SOGA1 Ensembl:ENSG00000149639 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:36815898..36816043 26863196 MeRIP-seq:(Medium) rs1236588085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_924874,Human_RBP_ID_8854433,Human_RBP_ID_9298480,Human_RBP_ID_18412916 RMVar_hsa_circ_108748,RMVar_hsa_circ_209896,RMVar_hsa_circ_290074,RMVar_hsa_circ_43114,RMVar_hsa_circ_209899,RMVar_hsa_circ_266929,RMVar_hsa_circ_83836,RMVar_hsa_circ_126199,RMVar_hsa_circ_348377,RMVar_hsa_circ_209903,RMVar_hsa_circ_209906,RMVar_hsa_circ_3935,RMVar_hsa_circ_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_378056,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209909 108211 RMVar_ID_108211 Human_SNP_ID_680146672 m1A Human chr20 + 36839404 36839404 36839404 GATACACGTCCTCCTCCATATAGACGTCCCGCATCTCCAGCATCTCGGCCCGCAGCTCCTCAATC GATACACGTCCTCCTCCATATAGACGTCCCGCTTCTCCAGCATCTCGGCCCGCAGCTCCTCAATC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36839325..36839422 26863196 MeRIP-seq:(Medium) rs1268990834 Functional Loss SNV dbSNP153 33..33 33 - - - 108212 RMVar_ID_108212 Human_SNP_ID_680149790 m1A Human chr20 + 36851419 36851419 36851419 CATACAGGCCCTGCCTGGCCTAAGCCCCGTCCACTTCTCCATCTTCATCTCCCTCGACGCCTCCT CATACAGGCCCTGCCTGGCCTAAGCCCCGTCCGCTTCTCCATCTTCATCTCCCTCGACGCCTCCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:36851417..36851650 26863196 MeRIP-seq:(Medium) rs149552879 Functional Loss SNV dbSNP153 33..33 33 - - - 108213 RMVar_ID_108213 Human_SNP_ID_680149802 m1A Human chr20 - 36851451 36851451 36851451 ACGACCCAAGTGGCTGCTGTGTTGCCAGTGAGAGGAGGCGTCGAGGGAGATGAAGATGGAGAAGT ACGACCCAAGTGGCTGCTGTGTTGCCAGTGAGGGGAGGCGTCGAGGGAGATGAAGATGGAGAAGT T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36851383..36851677 26863196 MeRIP-seq:(Medium) rs928842729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126199,RMVar_hsa_circ_209903 108214 RMVar_ID_108214 Human_SNP_ID_680152051 m1A Human chr20 - 36860179 36860179 36860179 AAGGGAAATTGGAATGCTCGTTGAGTTCAAGAACAGCGCTAAGGCCAGAGAGGGGAAGGAGTGTG AAGGGAAATTGGAATGCTCGTTGAGTTCAAGAGCAGCGCTAAGGCCAGAGAGGGGAAGGAGTGTG T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36860164..36860277 26863196 MeRIP-seq:(Medium) rs971016601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5652567 RMVar_hsa_circ_126199,RMVar_hsa_circ_209903 108215 RMVar_ID_108215 Human_SNP_ID_680175710 m1A Human chr20 + 36951577 36951577 36951577 GGACCAGTCTGCCTCTGCGGAAGGGGTGTTTGAGGGGGTTCTCGGGCTGTCATCGCAACGGGGAC GGACCAGTCTGCCTCTGCGGAAGGGGTGTTTGTGGGGGTTCTCGGGCTGTCATCGCAACGGGGAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36951528..36951656 26863196 MeRIP-seq:(Medium) rs886056649 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_699 108216 RMVar_ID_108216 Human_SNP_ID_680175722 m1A Human chr20 + 36951601 36951601 36951601 GGTGTTTGAGGGGGTTCTCGGGCTGTCATCGCAACGGGGACGCTTGGAGGGCTGCTCGGAATCGG GGTGTTTGAGGGGGTTCTCGGGCTGTCATCGCCACGGGGACGCTTGGAGGGCTGCTCGGAATCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:36951552..36951653 26863196 MeRIP-seq:(Medium) rs1235922763 Functional Loss SNV dbSNP153 33..33 33 - - - 108217 RMVar_ID_108217 Human_SNP_ID_680175727 m1A Human chr20 - 36951613 36951613 36951613 CCATGCAGCGAGCCGATTCCGAGCAGCCCTCCAAGCGTCCCCGTTGCGATGACAGCCCGAGAACC CCATGCAGCGAGCCGATTCCGAGCAGCCCTCCTAGCGTCCCCGTTGCGATGACAGCCCGAGAACC T A SAMHD1 Ensembl:ENSG00000101347 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:36951562..36951657;chr20:36951562..36951664 26863196 MeRIP-seq:(Medium) rs1346349736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659819 108218 RMVar_ID_108218 Human_SNP_ID_680234650 m1A Human chr20 + 37179189 37179189 37179189 GGAGGACTGGGATCCCGGCCGCGGCTGCTGGAAGCGTCGAAGCTCAGCGGGGCCGCGGACACTGA GGAGGACTGGGATCCCGGCCGCGGCTGCTGGAGGCGTCGAAGCTCAGCGGGGCCGCGGACACTGA A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:37179101..37179282 26863196 MeRIP-seq:(Medium) rs746048461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4645625,Human_RBP_ID_5240097,Human_RBP_ID_5323250,Human_RBP_ID_18193765 RMVar_hsa_circ_209971,RMVar_hsa_circ_123355,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_209970 108219 RMVar_ID_108219 Human_SNP_ID_680234659 m1A Human chr20 - 37179200 37179200 37179200 CTAAGCACAGGTCAGTGTCCGCGGCCCCGCTGAGCTTCGACGCTTCCAGCAGCCGCGGCCGGGAT CTAAGCACAGGTCAGTGTCCGCGGCCCCGCTGTGCTTCGACGCTTCCAGCAGCCGCGGCCGGGAT T A MROH8 Ensembl:ENSG00000101353 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37179132..37179470 26863196 MeRIP-seq:(Medium) rs1367153700 Functional Loss SNV dbSNP153 33..33 33 - - - 108220 RMVar_ID_108220 Human_SNP_ID_680236115 m1A Human chr20 - 37184192 37184192 37184192 TGCTGGCTATGATTGTCAGGGCCAACAGGAAGACAGTGCTTGAACCTTGGGGGGAAACAACCATT TGCTGGCTATGATTGTCAGGGCCAACAGGAAGGCAGTGCTTGAACCTTGGGGGGAAACAACCATT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37184176..37184225 26863196 MeRIP-seq:(Medium) rs1351475429 Functional Loss SNV dbSNP153 33..33 33 - - - 108221 RMVar_ID_108221 Human_SNP_ID_680236138 m1A Human chr20 + 37184249 37184249 37184249 AGCCAGCACCTGGGCTCTGACGCCCACTCACTACCTCACCAAGCATGACGTGGAGAGACTAAAAG AGCCAGCACCTGGGCTCTGACGCCCACTCACTGCCTCACCAAGCATGACGTGGAGAGACTAAAAG A G RPN2 Ensembl:ENSG00000118705 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:37184121..37184430 26863196 MeRIP-seq:(Medium) rs1414573866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659396,Human_RBP_ID_17396584,Human_RBP_ID_22422947,Human_RBP_ID_22453080,Human_RBP_ID_27485390 Human_Splice_Rec_2080776,Human_Splice_Rec_2080786,Human_Splice_Rec_2080818,Human_Splice_Rec_2080834,Human_Splice_Rec_2080844 Human_miRNA_ID_1915300,Human_miRNA_ID_1915301,Human_miRNA_ID_1917749,Human_miRNA_ID_1917750,Human_miRNA_ID_1920203,Human_miRNA_ID_1920204,Human_miRNA_ID_1922660,Human_miRNA_ID_1922661,Human_miRNA_ID_1925114,Human_miRNA_ID_1925115,Human_miRNA_ID_1927564,Human_miRNA_ID_1927565,Human_miRNA_ID_1930015,Human_miRNA_ID_1930016,Human_miRNA_ID_1932463,Human_miRNA_ID_1932464,Human_miRNA_ID_2007887,Human_miRNA_ID_2007888,Human_miRNA_ID_2168940,Human_miRNA_ID_2168941,Human_miRNA_ID_2170463,Human_miRNA_ID_2170464,Human_miRNA_ID_2383319,Human_miRNA_ID_2383320,Human_miRNA_ID_2630289,Human_miRNA_ID_2630290,Human_miRNA_ID_2643404,Human_miRNA_ID_2643405,Human_miRNA_ID_3126149,Human_miRNA_ID_3126150 RMVar_hsa_circ_90832,RMVar_hsa_circ_114205,RMVar_hsa_circ_209971,RMVar_hsa_circ_123355,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,RMVar_hsa_circ_328390,RMVar_hsa_circ_347488,RMVar_hsa_circ_209970,RMVar_hsa_circ_344552,RMVar_hsa_circ_277636,RMVar_hsa_circ_123005,RMVar_hsa_circ_100764,RMVar_hsa_circ_102647,RMVar_hsa_circ_93349,RMVar_hsa_circ_209975,RMVar_hsa_circ_209979,RMVar_hsa_circ_45372,RMVar_hsa_circ_84350,RMVar_hsa_circ_209981,RMVar_hsa_circ_209982,RMVar_hsa_circ_209983,RMVar_hsa_circ_209980,RMVar_hsa_circ_209977,RMVar_hsa_circ_209978,RMVar_hsa_circ_209976,RMVar_hsa_circ_209973,RMVar_hsa_circ_209974 108222 RMVar_ID_108222 Human_SNP_ID_680236163 m1A Human chr20 + 37184302 37184302 37184302 AGAGACTAAAAGCCTCGCTGGATCGCCCTTTCACAAATTTGGAATCTGCCTTCTACTCCATCGTG AGAGACTAAAAGCCTCGCTGGATCGCCCTTTCTCAAATTTGGAATCTGCCTTCTACTCCATCGTG A T RPN2 Ensembl:ENSG00000118705 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:37184251..37184325 26863196 MeRIP-seq:(Medium) rs759671052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62564,Human_RBP_ID_1596492,Human_RBP_ID_1929276,Human_RBP_ID_3647909,Human_RBP_ID_8532521,Human_RBP_ID_18772379,Human_RBP_ID_20624044,Human_RBP_ID_22453732,Human_RBP_ID_23115415,Human_RBP_ID_27296559,Human_RBP_ID_27485391 Human_Splice_Rec_2080777,Human_Splice_Rec_2080787,Human_Splice_Rec_2080819,Human_Splice_Rec_2080835,Human_Splice_Rec_2080845 Human_miRNA_ID_2720812,Human_miRNA_ID_2720813,Human_miRNA_ID_2933129,Human_miRNA_ID_2933130 RMVar_hsa_circ_90832,RMVar_hsa_circ_114205,RMVar_hsa_circ_209971,RMVar_hsa_circ_123355,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,RMVar_hsa_circ_328390,RMVar_hsa_circ_347488,RMVar_hsa_circ_209970,RMVar_hsa_circ_344552,RMVar_hsa_circ_277636,RMVar_hsa_circ_123005,RMVar_hsa_circ_100764,RMVar_hsa_circ_102647,RMVar_hsa_circ_93349,RMVar_hsa_circ_209975,RMVar_hsa_circ_209979,RMVar_hsa_circ_45372,RMVar_hsa_circ_84350,RMVar_hsa_circ_209981,RMVar_hsa_circ_209982,RMVar_hsa_circ_209983,RMVar_hsa_circ_209980,RMVar_hsa_circ_209977,RMVar_hsa_circ_209978,RMVar_hsa_circ_209976,RMVar_hsa_circ_209973,RMVar_hsa_circ_209974 108223 RMVar_ID_108223 Human_SNP_ID_680238483 m1A Human chr20 - 37193831 37193830 37193831 TCTATGCAGATAATTCTCAGACCCGTACCTCCAGCCCAGACTTCTCTCAACAGCCACTTACATGA TCTATGCAGATAATTCTCAGACCCGTACCTCC_GCCCAGACTTCTCTCAACAGCCACTTACATGA CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37193828..37194084 26863196 MeRIP-seq:(Medium) rs1433962797 Functional Loss DEL dbSNP153 33..33 33 - - - 108224 RMVar_ID_108224 Human_SNP_ID_680238560 m1A Human chr20 - 37194142 37194142 37194142 CCTCCACTCATTCCAATTTGGCTTCTGCCCCCAGCAGGCCAGTGGCAACCTCCAAATTGTCGAAG CCTCCACTCATTCCAATTTGGCTTCTGCCCCCGGCAGGCCAGTGGCAACCTCCAAATTGTCGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37194141..37194236 26863196 MeRIP-seq:(Medium) rs1239761798 Functional Loss SNV dbSNP153 33..33 33 - - - 108225 RMVar_ID_108225 Human_SNP_ID_680239279 m1A Human chr20 - 37196967 37196967 37196967 TGTTCACCTCTTCCTGACAGTCCTCCCAGGAGAGGCCAGGTATCCACCCTCTCAAGTGCTCCCCC TGTTCACCTCTTCCTGACAGTCCTCCCAGGAGCGGCCAGGTATCCACCCTCTCAAGTGCTCCCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37196962..37197262 26863196 MeRIP-seq:(Medium) rs1256527882 Functional Loss SNV dbSNP153 33..33 33 - - - 108226 RMVar_ID_108226 Human_SNP_ID_680239806 m1A Human chr20 + 37199142 37199142 37199142 GTTACCCAGATCTACCATGCAGTTGCAGCTCTAAGTGGCTTTGGCCTTCCCTTGGCATCCCAAGA GTTACCCAGATCTACCATGCAGTTGCAGCTCTGAGTGGCTTTGGCCTTCCCTTGGCATCCCAAGA A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1289792877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563448,Human_RBP_ID_1929282,Human_RBP_ID_4663268,Human_RBP_ID_17281358,Human_RBP_ID_17670873,Human_RBP_ID_22766987,Human_RBP_ID_26820833,Human_RBP_ID_27296564 Human_Splice_Rec_2080788,Human_Splice_Rec_2080789,Human_Splice_Rec_2080822,Human_Splice_Rec_2080823,Human_Splice_Rec_2080848,Human_Splice_Rec_2080849 RMVar_hsa_circ_114205,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,RMVar_hsa_circ_328390,RMVar_hsa_circ_347488,RMVar_hsa_circ_344552,RMVar_hsa_circ_123005,RMVar_hsa_circ_100764,RMVar_hsa_circ_102647,RMVar_hsa_circ_93349,RMVar_hsa_circ_209975,RMVar_hsa_circ_209979,RMVar_hsa_circ_45372,RMVar_hsa_circ_84350,RMVar_hsa_circ_209981,RMVar_hsa_circ_209980,RMVar_hsa_circ_209977,RMVar_hsa_circ_209978,RMVar_hsa_circ_209976,RMVar_hsa_circ_122194,RMVar_hsa_circ_209973,RMVar_hsa_circ_209974,RMVar_hsa_circ_286508,RMVar_hsa_circ_294621,RMVar_hsa_circ_317295,RMVar_hsa_circ_287729,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_91214,RMVar_hsa_circ_62103,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209985,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_209986,RMVar_hsa_circ_209984,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993 108227 RMVar_ID_108227 Human_SNP_ID_680247946 m1A Human chr20 - 37232352 37232352 37232352 AAGAGCAGAAGCAACGGCGAGAGGATCAGGGCAGTGAATGTATTGGACACCACGGTGGGGGGCCT AAGAGCAGAAGCAACGGCGAGAGGATCAGGGCGGTGAATGTATTGGACACCACGGTGGGGGGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:37232255..37232425 26863196 MeRIP-seq:(Medium) rs376104849 Functional Loss SNV dbSNP153 33..33 33 - - - 108228 RMVar_ID_108228 Human_SNP_ID_680247947 m1A Human chr20 - 37232352 37232352 37232352 AAGAGCAGAAGCAACGGCGAGAGGATCAGGGCAGTGAATGTATTGGACACCACGGTGGGGGGCCT AAGAGCAGAAGCAACGGCGAGAGGATCAGGGCCGTGAATGTATTGGACACCACGGTGGGGGGCCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:37232255..37232425 26863196 MeRIP-seq:(Medium) rs376104849 Functional Loss SNV dbSNP153 33..33 33 - - - 108229 RMVar_ID_108229 Human_SNP_ID_680250043 m1A Human chr20 + 37241325 37241321 37241325 TTTCTTTCAGAACAGCACATTAGTTCCAGAAGAAAGATGGAAATTCTGAAAACTGAATGTCAAGA TTTCTTTCAGAACAGCACATTAGTTCCAG____AAGATGGAAATTCTGAAAACTGAATGTCAAGA GAAGA G RPN2 Ensembl:ENSG00000118705 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:37241301..37241375 32194978 MeRIP-seq:(Medium) rs1232153205 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_62589,Human_RBP_ID_1929310,Human_RBP_ID_4663289,Human_RBP_ID_5595064,Human_RBP_ID_17658884,Human_RBP_ID_20624057,Human_RBP_ID_23903588,Human_RBP_ID_24546859,Human_RBP_ID_26490167 Human_Splice_Rec_2080816,Human_Splice_Rec_2080874,Human_Splice_Rec_2080882,Human_Splice_Rec_2080890,Human_Splice_Rec_2080896 RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123005,RMVar_hsa_circ_209973,RMVar_hsa_circ_209991,RMVar_hsa_circ_79324,RMVar_hsa_circ_115210,RMVar_hsa_circ_210003,RMVar_hsa_circ_113989,RMVar_hsa_circ_121305,RMVar_hsa_circ_210016,RMVar_hsa_circ_111219,RMVar_hsa_circ_210019,RMVar_hsa_circ_210020,RMVar_hsa_circ_88730,RMVar_hsa_circ_210025 108230 RMVar_ID_108230 Human_SNP_ID_680250045 m1A Human chr20 + 37241325 37241324 37241325 TTTCTTTCAGAACAGCACATTAGTTCCAGAAGAAAGATGGAAATTCTGAAAACTGAATGTCAAGA TTTCTTTCAGAACAGCACATTAGTTCCAGAAG_AAGATGGAAATTCTGAAAACTGAATGTCAAGA GA G RPN2 Ensembl:ENSG00000118705 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:37241301..37241375 32194978 MeRIP-seq:(Medium) rs1487377235 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_62589,Human_RBP_ID_1929310,Human_RBP_ID_4663289,Human_RBP_ID_5595064,Human_RBP_ID_17658884,Human_RBP_ID_20624057,Human_RBP_ID_23903588,Human_RBP_ID_24546859,Human_RBP_ID_26490167 Human_Splice_Rec_2080816,Human_Splice_Rec_2080874,Human_Splice_Rec_2080882,Human_Splice_Rec_2080890,Human_Splice_Rec_2080896 RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123005,RMVar_hsa_circ_209973,RMVar_hsa_circ_209991,RMVar_hsa_circ_79324,RMVar_hsa_circ_115210,RMVar_hsa_circ_210003,RMVar_hsa_circ_113989,RMVar_hsa_circ_121305,RMVar_hsa_circ_210016,RMVar_hsa_circ_111219,RMVar_hsa_circ_210019,RMVar_hsa_circ_210020,RMVar_hsa_circ_88730,RMVar_hsa_circ_210025 108231 RMVar_ID_108231 Human_SNP_ID_680261989 m1A Human chr20 + 37289685 37289685 37289685 CTACTTCCGGGGGAGCGGCGCGGCGGCGCGGGAGGTGAGTGCCGCAGCTTTGCGGTGGGGTGGGA CTACTTCCGGGGGAGCGGCGCGGCGGCGCGGGGGGTGAGTGCCGCAGCTTTGCGGTGGGGTGGGA A G MANBAL Ensembl:ENSG00000101363 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:37289669..37289814;chr20:37289651..37289850;chr20:37289651..37289889 26863196 MeRIP-seq:(Medium) rs867811290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2080917,Human_Splice_Rec_2080921,Human_Splice_Rec_2080927 RMVar_hsa_circ_82189,RMVar_hsa_circ_210026 108232 RMVar_ID_108232 Human_SNP_ID_680261990 m1A Human chr20 - 37289688 37289688 37289688 GGTTCCCACCCCACCGCAAAGCTGCGGCACTCACCTCCCGCGCCGCCGCGCCGCTCCCCCGGAAG GGTTCCCACCCCACCGCAAAGCTGCGGCACTCCCCTCCCGCGCCGCCGCGCCGCTCCCCCGGAAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:37289677..37289828 26863196 MeRIP-seq:(Medium) rs1244685911 Functional Loss SNV dbSNP153 33..33 33 - - - 108233 RMVar_ID_108233 Human_SNP_ID_680264283 m1A Human chr20 - 37298805 37298805 37298805 TCCAGCTGGGAGGTCTAGGCTGCAGTGAGCCAATGAGTCGTGATTGCGCCACCCTGAGTGACGGG TCCAGCTGGGAGGTCTAGGCTGCAGTGAGCCAGTGAGTCGTGATTGCGCCACCCTGAGTGACGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37298802..37301425 26863196 MeRIP-seq:(Medium) rs1352626577 Functional Loss SNV dbSNP153 33..33 33 - - - 108234 RMVar_ID_108234 Human_SNP_ID_680266033 m1A Human chr20 + 37306023 37306023 37306023 TTTTAACATGGGGACGGGGTACTCTTAGGGAGAAAGGGAGCCCATGGGAGTGGGGGCAGCTTGTA TTTTAACATGGGGACGGGGTACTCTTAGGGAGGAAGGGAGCCCATGGGAGTGGGGGCAGCTTGTA A G MANBAL Ensembl:ENSG00000101363 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37306021..37306143 26863196 MeRIP-seq:(Medium) rs1231850477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6998107 RMVar_hsa_circ_99280,RMVar_hsa_circ_95300,RMVar_hsa_circ_210027,RMVar_hsa_circ_210029 108235 RMVar_ID_108235 Human_SNP_ID_680266998 m1A Human chr20 - 37310276 37310276 37310276 GGGAGCTGAGAAGGCCTCGCAGAGATGAAACTAGCAGTGGCCTTGAGGAAAGATAGGACTGGCTG GGGAGCTGAGAAGGCCTCGCAGAGATGAAACTGGCAGTGGCCTTGAGGAAAGATAGGACTGGCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:37310273..37310373 32194978 MeRIP-seq:(Medium) rs1232381676 Functional Loss SNV dbSNP153 33..33 33 - - - 108236 RMVar_ID_108236 Human_SNP_ID_680268456 m1A Human chr20 + 37316401 37316401 37316401 CTTCTGTGAACAAGAGGCCCAAGAAAGAGACTAAGAAGAAGCGGTAGAAGAGGAGGCCTGAGGAG CTTCTGTGAACAAGAGGCCCAAGAAAGAGACTGAGAAGAAGCGGTAGAAGAGGAGGCCTGAGGAG A G MANBAL Ensembl:ENSG00000101363 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:37316351..37316575 26863196 MeRIP-seq:(Medium) rs766520130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563515,Human_RBP_ID_4645766 Human_Splice_Rec_2080920,Human_Splice_Rec_2080926,Human_Splice_Rec_2080934,Human_Splice_Rec_2080940,Human_Splice_Rec_2080946 RMVar_hsa_circ_99280,RMVar_hsa_circ_95300,RMVar_hsa_circ_210027,RMVar_hsa_circ_210029 108237 RMVar_ID_108237 Human_SNP_ID_680278727 m1A Human chr20 - 37359483 37359483 37359483 AGCTTCTTTGAGGTGTGAAGCCTTCCCTGGCCACCATCTAATTGCGACCCATCCTCCACGAGCCC AGCTTCTTTGAGGTGTGAAGCCTTCCCTGGCCGCCATCTAATTGCGACCCATCCTCCACGAGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37359477..37359560 26863196 MeRIP-seq:(Medium) rs1216700738 Functional Loss SNV dbSNP153 33..33 33 - - - 108238 RMVar_ID_108238 Human_SNP_ID_680286484 m1A Human chr20 - 37389389 37389389 37389389 CCCGAGGTGCCCCCTGCCGCCATGCCGGGGGCAAGGAGGCAGAGGCCAGCTGAGGCGCTGTTGCC CCCGAGGTGCCCCCTGCCGCCATGCCGGGGGCCAGGAGGCAGAGGCCAGCTGAGGCGCTGTTGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:37389387..37389577 32194978 MeRIP-seq:(Medium) rs1422762835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210036 108239 RMVar_ID_108239 Human_SNP_ID_680316468 m1A Human chr20 - 37504538 37504534 37504538 AAATAAAAGGAAGGGCCTGAGAGATGCGACAAACAACCAGGAGAGGGGGTTGCCATGACAACCAA AAATAAAAGGAAGGGCCTGAGAGATGCGACAA____CCAGGAGAGGGGGTTGCCATGACAACCAA GTTGT G BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37504487..37504788 26863196 MeRIP-seq:(Medium) rs1300175959 Functional Loss DEL dbSNP153 33..36 33 - - - 108240 RMVar_ID_108240 Human_SNP_ID_680316469 m1A Human chr20 - 37504538 37504538 37504538 AAATAAAAGGAAGGGCCTGAGAGATGCGACAAACAACCAGGAGAGGGGGTTGCCATGACAACCAA AAATAAAAGGAAGGGCCTGAGAGATGCGACAAGCAACCAGGAGAGGGGGTTGCCATGACAACCAA T C BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37504487..37504788 26863196 MeRIP-seq:(Medium) rs752936750 Functional Loss SNV dbSNP153 33..33 33 - - - 108241 RMVar_ID_108241 Human_SNP_ID_680316470 m1A Human chr20 - 37504538 37504538 37504538 AAATAAAAGGAAGGGCCTGAGAGATGCGACAAACAACCAGGAGAGGGGGTTGCCATGACAACCAA AAATAAAAGGAAGGGCCTGAGAGATGCGACAACCAACCAGGAGAGGGGGTTGCCATGACAACCAA T G BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37504487..37504788 26863196 MeRIP-seq:(Medium) rs752936750 Functional Loss SNV dbSNP153 33..33 33 - - - 108242 RMVar_ID_108242 Human_SNP_ID_680317027 m1A Human chr20 + 37507128 37507128 37507128 GCCACCTCCTCCTGGATGCCCACCTCTGACTCAACCTGTCCAAAATTGAGCTCAATAACTTTCTC GCCACCTCCTCCTGGATGCCCACCTCTGACTCCACCTGTCCAAAATTGAGCTCAATAACTTTCTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37507081..37507383 26863196 MeRIP-seq:(Medium) rs901857117 Functional Loss SNV dbSNP153 33..33 33 - - - 108243 RMVar_ID_108243 Human_SNP_ID_680319879 m1A Human chr20 + 37519113 37519113 37519113 AGAAGCCCATGAACATGGAGTGGCTGAACCACAGGGCGGGGTTGAGGGGCTTGGGGATGAGGAGG AGAAGCCCATGAACATGGAGTGGCTGAACCACTGGGCGGGGTTGAGGGGCTTGGGGATGAGGAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:37519064..37519188 26863196 MeRIP-seq:(Medium) rs878906085 Functional Loss SNV dbSNP153 33..33 33 - - - 108244 RMVar_ID_108244 Human_SNP_ID_680319939 m1A Human chr20 - 37519282 37519282 37519282 AGAGAGCACAGCGGCTCAGCTCCTGGAGAGTGAGGGTTGAAGAAAGCGGAGGGCAGCCGCCTGCG AGAGAGCACAGCGGCTCAGCTCCTGGAGAGTGCGGGTTGAAGAAAGCGGAGGGCAGCCGCCTGCG T G BLCAP Ensembl:ENSG00000166619 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37519151..37519375 26863196 MeRIP-seq:(Medium) rs892459815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563611,Human_RBP_ID_4659401,Human_RBP_ID_6998283,Human_RBP_ID_8942832,Human_RBP_ID_14096640 Human_Splice_Rec_2081080,Human_Splice_Rec_2081081,Human_Splice_Rec_2081086,Human_Splice_Rec_2081088,Human_Splice_Rec_2081092,Human_Splice_Rec_2081094,Human_Splice_Rec_2081096,Human_Splice_Rec_2081098,Human_Splice_Rec_2081100,Human_Splice_Rec_2081104,Human_Splice_Rec_2081108,Human_Splice_Rec_2081110 RMVar_hsa_circ_112239,RMVar_hsa_circ_210041 108245 RMVar_ID_108245 Human_SNP_ID_680320654 m1A Human chr20 - 37521502 37521502 37521502 CACTTGGGCAGGCAAGGATCGCGGCAATCGGAATAGGACGGGTCCGGGAAGCGGCAATCGCGACG CACTTGGGCAGGCAAGGATCGCGGCAATCGGAGTAGGACGGGTCCGGGAAGCGGCAATCGCGACG T C BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:37521451..37521657 26863196 MeRIP-seq:(Medium) rs567277107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5200748,Human_RBP_ID_6998298,Human_RBP_ID_14096692,Human_RBP_ID_22417628,Human_RBP_ID_26788418 RMVar_hsa_circ_210042,RMVar_hsa_circ_112239,RMVar_hsa_circ_210041 108246 RMVar_ID_108246 Human_SNP_ID_680322203 m1A Human chr20 + 37527200 37527200 37527200 GTTCCTTCAGCTGCCCTTGAGGGCCACTCCCCACGTCTATAGAAGGAAAGGGAAGGGATGTCCAC GTTCCTTCAGCTGCCCTTGAGGGCCACTCCCCGCGTCTATAGAAGGAAAGGGAAGGGATGTCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:37527198..37527289 26863196 MeRIP-seq:(Medium) rs1053546894 Functional Loss SNV dbSNP153 33..33 33 - - - 108247 RMVar_ID_108247 Human_SNP_ID_680322412 m1A Human chr20 - 37527843 37527843 37527843 CTGCGGCGTCGGTGGCGAGCTGAGGTGGAGGCAGGCTGCGGCAGACGGCGACAGTGGCGGCGGCG CTGCGGCGTCGGTGGCGAGCTGAGGTGGAGGCGGGCTGCGGCAGACGGCGACAGTGGCGGCGGCG T C BLCAP Ensembl:ENSG00000166619 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:37527744..37527900;chr20:37527654..37527900;chr20:37527703..37527900 26863196 MeRIP-seq:(Medium) rs1429362112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244885,Human_RBP_ID_563612,Human_RBP_ID_4659404,Human_RBP_ID_19106434 Human_Splice_Rec_2081079,Human_Splice_Rec_2081087,Human_Splice_Rec_2081089,Human_Splice_Rec_2081101,Human_Splice_Rec_2081105 108248 RMVar_ID_108248 Human_SNP_ID_680363778 m1A Human chr20 + 37694101 37694101 37694101 CCCGCGGTCTGGGCGTGAGTGCAGGGAAGTGGAGTATTTGCTGGGCCGGGTACCATGGACGTGGG CCCGCGGTCTGGGCGTGAGTGCAGGGAAGTGGTGTATTTGCTGGGCCGGGTACCATGGACGTGGG A T CTNNBL1 Ensembl:ENSG00000132792 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:37694051..37694979 26863196 MeRIP-seq:(Medium) rs758242514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659831,Human_RBP_ID_9390591,Human_RBP_ID_27819753 Human_Splice_Rec_2081157,Human_Splice_Rec_2081187,Human_Splice_Rec_2081219,Human_Splice_Rec_2081247,Human_Splice_Rec_2081257 108249 RMVar_ID_108249 Human_SNP_ID_680372464 m1A Human chr20 + 37732958 37732958 37732958 GAAGATGCGTCGGAAACAAACTGGTACTCGAGAACGCGGCCGCTATCGGGAAGAAGAAATGACTG GAAGATGCGTCGGAAACAAACTGGTACTCGAGGACGCGGCCGCTATCGGGAAGAAGAAATGACTG A G CTNNBL1 Ensembl:ENSG00000132792 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:37727396..37737433 26863196 MeRIP-seq:(Medium) rs1292467483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5595065,Human_RBP_ID_9389175,Human_RBP_ID_19005673,Human_RBP_ID_23001952,Human_RBP_ID_24546809,Human_RBP_ID_26342443 Human_Splice_Rec_2081160,Human_Splice_Rec_2081188,Human_Splice_Rec_2081220,Human_Splice_Rec_2081250,Human_Splice_Rec_2081260 Human_miRNA_ID_2791120,Human_miRNA_ID_2791121 RMVar_hsa_circ_69574,RMVar_hsa_circ_210047,RMVar_hsa_circ_338849,RMVar_hsa_circ_341476,RMVar_hsa_circ_117586,RMVar_hsa_circ_210048,RMVar_hsa_circ_378548 108250 RMVar_ID_108250 Human_SNP_ID_680387664 m1A Human chr20 + 37803009 37803009 37803009 CCATCTTTCCCCTCTTTATGAAATCTCCCAGGAAGATCAAGAAAGTGGGAACCACTGAGAAGGAA CCATCTTTCCCCTCTTTATGAAATCTCCCAGGCAGATCAAGAAAGTGGGAACCACTGAGAAGGAA A C CTNNBL1 Ensembl:ENSG00000132792 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:37779229..37803011 32194978 MeRIP-seq:(Medium) rs937079115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1929363,Human_RBP_ID_8532722 Human_Splice_Rec_2081177,Human_Splice_Rec_2081209,Human_Splice_Rec_2081237,Human_Splice_Rec_2081277,Human_Splice_Rec_2081301,Human_Splice_Rec_2081329,Human_Splice_Rec_2081347 Human_miRNA_ID_2041657,Human_miRNA_ID_3020635 RMVar_hsa_circ_3192,RMVar_hsa_circ_210047,RMVar_hsa_circ_117586,RMVar_hsa_circ_266392,RMVar_hsa_circ_360996,RMVar_hsa_circ_276674,RMVar_hsa_circ_85226,RMVar_hsa_circ_210052,RMVar_hsa_circ_210053,RMVar_hsa_circ_90948,RMVar_hsa_circ_298958,RMVar_hsa_circ_210056,RMVar_hsa_circ_47538,RMVar_hsa_circ_210055,RMVar_hsa_circ_3093,RMVar_hsa_circ_88667,RMVar_hsa_circ_335692,RMVar_hsa_circ_31400,RMVar_hsa_circ_210058 108251 RMVar_ID_108251 Human_SNP_ID_680395681 m1A Human chr20 - 37840166 37840166 37840166 TTCTCACTGTCATTTTCAGTGAATTTATTCAGAAGCCGGGTCCGCTGCTGCCCTCTCAGGTTCCG TTCTCACTGTCATTTTCAGTGAATTTATTCAGTAGCCGGGTCCGCTGCTGCCCTCTCAGGTTCCG T A lnc-TTI1-3,lnc-TTI1-3:2 RNACentral:URS00008B5B98,RNACentral:URS00008B9B26 lincRNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:37840115..37872029 32194978 MeRIP-seq:(Medium) rs1401693853 Functional Loss SNV dbSNP153 33..33 33 - - - 108252 RMVar_ID_108252 Human_SNP_ID_680411079 m1A Human chr20 + 37903078 37903078 37903078 GGGAGGGGAGGAGGGAGGCGGGAGGAGGGAGGAGGGTGCGGCGGCGGCGCGGCGTGGCCTTCCGC GGGAGGGGAGGAGGGAGGCGGGAGGAGGGAGGCGGGTGCGGCGGCGGCGCGGCGTGGCCTTCCGC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:37903075..37903204 26863196 MeRIP-seq:(Medium) rs1370544795 Functional Loss SNV dbSNP153 33..33 33 - - - 108253 RMVar_ID_108253 Human_SNP_ID_680411133 m1A Human chr20 - 37903177 37903177 37903177 CCCAGCTCCCAGCCCTCGCCCGGCTCCGGCCCAGCCCCGGCTTCGGGGAGCGAGCGCACGCCCAG CCCAGCTCCCAGCCCTCGCCCGGCTCCGGCCCGGCCCCGGCTTCGGGGAGCGAGCGCACGCCCAG T C HSALNG0129929 RNACentral:URS0000EBCD9C lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr20:37903147..37903294;chr20:37903146..37903231 26863196,26863410 MeRIP-seq:(Medium) rs898643225 Functional Loss SNV dbSNP153 33..33 33 - - - 108254 RMVar_ID_108254 Human_SNP_ID_680421435 m1A Human chr20 - 37943967 37943967 37943967 TGCCCACCACCTTGACCACCTGGGGGTGACAGAGAGACCGTGACCTGTCCATCCAGTGACAGTGG TGCCCACCACCTTGACCACCTGGGGGTGACAGGGAGACCGTGACCTGTCCATCCAGTGACAGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37943965..37944037 26863196 MeRIP-seq:(Medium) rs1003346820 Functional Loss SNV dbSNP153 33..33 33 - - - 108255 RMVar_ID_108255 Human_SNP_ID_680421589 m1A Human chr20 - 37944265 37944264 37944265 TCTGTACAGCGTGGGGGCGGATGGGCGGGGGCAGGGGCATCAGTCTAGAGGCTGCAGGCCTCCTG TCTGTACAGCGTGGGGGCGGATGGGCGGGGGC_GGGGCATCAGTCTAGAGGCTGCAGGCCTCCTG CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37944217..37944398 26863196 MeRIP-seq:(Medium) rs1322905609 Functional Loss DEL dbSNP153 33..33 33 - - - 108256 RMVar_ID_108256 Human_SNP_ID_680421590 m1A Human chr20 - 37944265 37944265 37944265 TCTGTACAGCGTGGGGGCGGATGGGCGGGGGCAGGGGCATCAGTCTAGAGGCTGCAGGCCTCCTG TCTGTACAGCGTGGGGGCGGATGGGCGGGGGCGGGGGCATCAGTCTAGAGGCTGCAGGCCTCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37944217..37944398 26863196 MeRIP-seq:(Medium) rs1201911159 Functional Loss SNV dbSNP153 33..33 33 - - - 108257 RMVar_ID_108257 Human_SNP_ID_680429531 m1A Human chr20 + 37977343 37977333 37977343 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGG__________CGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG GGGGGGGGAGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1568853903 Functional Loss DEL dbSNP153 24..33 33 - - - 108258 RMVar_ID_108258 Human_SNP_ID_680429545 m1A Human chr20 + 37977343 37977339 37977344 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGGGGGGGG_____GGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG GGAGAC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1408545193 Functional Loss DEL dbSNP153 30..34 33 - - - 108259 RMVar_ID_108259 Human_SNP_ID_680429548 m1A Human chr20 + 37977343 37977340 37977344 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGGGGGGGGG____GGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG GAGAC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1349677138 Functional Loss DEL dbSNP153 31..34 33 - - - 108260 RMVar_ID_108260 Human_SNP_ID_680429549 m1A Human chr20 + 37977343 37977340 37977343 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGGGGGGGGG___CGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG GAGA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1407743527 Functional Loss DEL dbSNP153 31..33 33 - - - 108261 RMVar_ID_108261 Human_SNP_ID_680429551 m1A Human chr20 + 37977343 37977342 37977344 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAG__GGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG GAC G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1332097545 Functional Loss DEL dbSNP153 33..34 33 - - - 108262 RMVar_ID_108262 Human_SNP_ID_680429552 m1A Human chr20 + 37977343 37977343 37977343 AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGACGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG AGTGGGGGAGACGGGGGCGGGGGGGGGGGGAGGCGGGGGCGGGGGGGCGGGGGGGGGCGGCGCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:37977301..37977375 26863196 MeRIP-seq:(Medium) rs1234958206 Functional Loss SNV dbSNP153 33..33 33 - - - 108263 RMVar_ID_108263 Human_SNP_ID_680446824 m1A Human chr20 + 38046607 38046606 38046608 AGTGTTATTTTCAACGTGGAGATTAGGGAATGACACACTGAAGGTGGTGTAACTAAACATACCCC AGTGTTATTTTCAACGTGGAGATTAGGGAATG__ACACTGAAGGTGGTGTAACTAAACATACCCC GAC G RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:38046550..38046726 26863196 MeRIP-seq:(Medium) rs564315223 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14098991 RMVar_hsa_circ_210075,RMVar_hsa_circ_265836,RMVar_hsa_circ_278927,RMVar_hsa_circ_274845,RMVar_hsa_circ_38148,RMVar_hsa_circ_210074 108264 RMVar_ID_108264 Human_SNP_ID_680446825 m1A Human chr20 + 38046607 38046607 38046607 AGTGTTATTTTCAACGTGGAGATTAGGGAATGACACACTGAAGGTGGTGTAACTAAACATACCCC AGTGTTATTTTCAACGTGGAGATTAGGGAATGGCACACTGAAGGTGGTGTAACTAAACATACCCC A G RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:38046550..38046726 26863196 MeRIP-seq:(Medium) rs1342470418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14098991 RMVar_hsa_circ_210075,RMVar_hsa_circ_265836,RMVar_hsa_circ_278927,RMVar_hsa_circ_274845,RMVar_hsa_circ_38148,RMVar_hsa_circ_210074 108265 RMVar_ID_108265 Human_SNP_ID_680450950 m1A Human chr20 + 38063648 38063648 38063648 AGGTTTGTGTGCTAGTGGTTTTCTTAGGAGGGAGAGAGAGAATTTGCTGAGGTAGAGAAGACATG AGGTTTGTGTGCTAGTGGTTTTCTTAGGAGGGGGAGAGAGAATTTGCTGAGGTAGAGAAGACATG A G RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38063599..38063804 26863196 MeRIP-seq:(Medium) rs189788594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6998991,Human_RBP_ID_14099372,Human_RBP_ID_27701694 RMVar_hsa_circ_210075,RMVar_hsa_circ_265836,RMVar_hsa_circ_274845,RMVar_hsa_circ_210077,RMVar_hsa_circ_320211,RMVar_hsa_circ_278529,RMVar_hsa_circ_377911,RMVar_hsa_circ_210078 108266 RMVar_ID_108266 Human_SNP_ID_680457104 m1A Human chr20 - 38088884 38088884 38088884 CAAAGCCTGGCCTCCACTCCTCTGCTCCTTGGACTATCTGGACTCCACCTCTCTAGGAAAATCCT CAAAGCCTGGCCTCCACTCCTCTGCTCCTTGGTCTATCTGGACTCCACCTCTCTAGGAAAATCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:38088873..38088970 26863196 MeRIP-seq:(Medium) rs1035360005 Functional Loss SNV dbSNP153 33..33 33 - - - 108267 RMVar_ID_108267 Human_SNP_ID_680470992 m1A Human chr20 + 38142199 38142199 38142199 CGACGCGGGTAGGGATGCCCAGGCACCTCAGCACTGTTGGAGAGGAGTGGAAAGCGGGGTGAGGT CGACGCGGGTAGGGATGCCCAGGCACCTCAGCGCTGTTGGAGAGGAGTGGAAAGCGGGGTGAGGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:38139425..38145430 32194978 MeRIP-seq:(Medium) rs762541606 Functional Loss SNV dbSNP153 33..33 33 - - - 108268 RMVar_ID_108268 Human_SNP_ID_680476156 m1A Human chr20 - 38161508 38161508 38161508 GCCGACCTGTGCCGGGAGAAGCTGGTGGTGCGACGGGGCCAGCCCTTCTGGCTGACCCTGCACTT GCCGACCTGTGCCGGGAGAAGCTGGTGGTGCGGCGGGGCCAGCCCTTCTGGCTGACCCTGCACTT T C TGM2 Ensembl:ENSG00000198959 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:38161459..38161560 32194978 MeRIP-seq:(Medium) rs530596287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_926602,Human_RBP_ID_4659835,Human_RBP_ID_8857508 Human_Splice_Rec_2081480,Human_Splice_Rec_2081481,Human_Splice_Rec_2081508,Human_Splice_Rec_2081509,Human_Splice_Rec_2081526,Human_Splice_Rec_2081527,Human_Splice_Rec_2081538,Human_Splice_Rec_2081539,Human_Splice_Rec_2081550,Human_Splice_Rec_2081551 RMVar_hsa_circ_375126,RMVar_hsa_circ_210084 108269 RMVar_ID_108269 Human_SNP_ID_680476185 m1A Human chr20 + 38161559 38161559 38161559 CGGCACAGGTCGGCCGTGTGGTGGTCTCGGCCATTGGTCTCCAGCTCCAGATCACACCTCTCTAA CGGCACAGGTCGGCCGTGTGGTGGTCTCGGCCGTTGGTCTCCAGCTCCAGATCACACCTCTCTAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38161509..38161645 26863196 MeRIP-seq:(Medium) rs746925553 Functional Loss SNV dbSNP153 33..33 33 - - - 108270 RMVar_ID_108270 Human_SNP_ID_680477117 m1A Human chr20 + 38165245 38165215 38165246 GGTGGCTCCTTCCACTGGCGGCGAGACCCTCCAAGTGCGACCACTGGCGGCTGGCACTGCCGAGG GGT_______________________________GTGCGACCACTGGCGGCTGGCACTGCCGAGG TGGCTCCTTCCACTGGCGGCGAGACCCTCCAA T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38165134..38165245 26863196 MeRIP-seq:(Medium) rs1568708905 Functional Loss DEL dbSNP153 4..34 33 - - - 108271 RMVar_ID_108271 Human_SNP_ID_680477133 m1A Human chr20 + 38165245 38165245 38165245 GGTGGCTCCTTCCACTGGCGGCGAGACCCTCCAAGTGCGACCACTGGCGGCTGGCACTGCCGAGG GGTGGCTCCTTCCACTGGCGGCGAGACCCTCCGAGTGCGACCACTGGCGGCTGGCACTGCCGAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38165134..38165245 26863196 MeRIP-seq:(Medium) rs771002016 Functional Loss SNV dbSNP153 33..33 33 - - - 108272 RMVar_ID_108272 Human_SNP_ID_680544725 m1A Human chr20 + 38426986 38426986 38426986 AGATGTAAAGATGCTACCCTATCCTGTCCCCAAGTTACACATACACACACACACACACACACACA AGATGTAAAGATGCTACCCTATCCTGTCCCCAGGTTACACATACACACACACACACACACACACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:38426981..38427132 26863196 MeRIP-seq:(Medium) rs73905616 Functional Loss SNV dbSNP153 33..33 33 - - - 108273 RMVar_ID_108273 Human_SNP_ID_680546887 m1A Human chr20 - 38435261 38435261 38435261 CACGCCACCGCACCCCATCTCTCGAAATCTGCAGACATCTTGATTTTTCCCACGCTGTCTGTCAG CACGCCACCGCACCCCATCTCTCGAAATCTGCCGACATCTTGATTTTTCCCACGCTGTCTGTCAG T G SNHG17 Ensembl:ENSG00000196756 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:38435167..38435304 26863410 MeRIP-seq:(Medium) rs905823063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1596924,Human_RBP_ID_3657045,Human_RBP_ID_5201634,Human_RBP_ID_5423719,Human_RBP_ID_5445606,Human_RBP_ID_5596022,Human_RBP_ID_8533055,Human_RBP_ID_9390614,Human_RBP_ID_14102403,Human_RBP_ID_18772844,Human_RBP_ID_23002085 Human_Splice_Rec_2081769,Human_Splice_Rec_2081797,Human_Splice_Rec_2081823,Human_Splice_Rec_2081833,Human_Splice_Rec_2081923,Human_Splice_Rec_2081933,Human_Splice_Rec_2081953,Human_Splice_Rec_2082013,Human_Splice_Rec_2082025,Human_Splice_Rec_2082051,Human_Splice_Rec_2082099,Human_Splice_Rec_2082113,Human_Splice_Rec_2082161,Human_Splice_Rec_2082177,Human_Splice_Rec_2082305,Human_Splice_Rec_2082317,Human_Splice_Rec_2082355,Human_Splice_Rec_2082371,Human_Splice_Rec_2082413,Human_Splice_Rec_2082437,Human_Splice_Rec_2082475,Human_Splice_Rec_2082569,Human_Splice_Rec_2082601,Human_Splice_Rec_2082615 108274 RMVar_ID_108274 Human_SNP_ID_680546897 m1A Human chr20 - 38435292 38435292 38435292 CTTCGCCGTCCCTCGCCGTCCTTCGCCATCGCACGCCACCGCACCCCATCTCTCGAAATCTGCAG CTTCGCCGTCCCTCGCCGTCCTTCGCCATCGCTCGCCACCGCACCCCATCTCTCGAAATCTGCAG T A SNHG17 Ensembl:ENSG00000196756 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:38435176..38435375 26863196 MeRIP-seq:(Medium) rs891868422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3657045,Human_RBP_ID_9390614,Human_RBP_ID_14102403 Human_Splice_Rec_2081769,Human_Splice_Rec_2081797,Human_Splice_Rec_2081823,Human_Splice_Rec_2081833,Human_Splice_Rec_2081923,Human_Splice_Rec_2081933,Human_Splice_Rec_2081953,Human_Splice_Rec_2082013,Human_Splice_Rec_2082025,Human_Splice_Rec_2082051,Human_Splice_Rec_2082099,Human_Splice_Rec_2082113,Human_Splice_Rec_2082161,Human_Splice_Rec_2082177,Human_Splice_Rec_2082305,Human_Splice_Rec_2082317,Human_Splice_Rec_2082355,Human_Splice_Rec_2082371,Human_Splice_Rec_2082413,Human_Splice_Rec_2082437,Human_Splice_Rec_2082475,Human_Splice_Rec_2082569,Human_Splice_Rec_2082601,Human_Splice_Rec_2082615 108275 RMVar_ID_108275 Human_SNP_ID_680546898 m1A Human chr20 - 38435292 38435292 38435292 CTTCGCCGTCCCTCGCCGTCCTTCGCCATCGCACGCCACCGCACCCCATCTCTCGAAATCTGCAG CTTCGCCGTCCCTCGCCGTCCTTCGCCATCGCCCGCCACCGCACCCCATCTCTCGAAATCTGCAG T G SNHG17 Ensembl:ENSG00000196756 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:38435176..38435375 26863196 MeRIP-seq:(Medium) rs891868422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3657045,Human_RBP_ID_9390614,Human_RBP_ID_14102403 Human_Splice_Rec_2081769,Human_Splice_Rec_2081797,Human_Splice_Rec_2081823,Human_Splice_Rec_2081833,Human_Splice_Rec_2081923,Human_Splice_Rec_2081933,Human_Splice_Rec_2081953,Human_Splice_Rec_2082013,Human_Splice_Rec_2082025,Human_Splice_Rec_2082051,Human_Splice_Rec_2082099,Human_Splice_Rec_2082113,Human_Splice_Rec_2082161,Human_Splice_Rec_2082177,Human_Splice_Rec_2082305,Human_Splice_Rec_2082317,Human_Splice_Rec_2082355,Human_Splice_Rec_2082371,Human_Splice_Rec_2082413,Human_Splice_Rec_2082437,Human_Splice_Rec_2082475,Human_Splice_Rec_2082569,Human_Splice_Rec_2082601,Human_Splice_Rec_2082615 108276 RMVar_ID_108276 Human_SNP_ID_680549823 m1A Human chr20 + 38446730 38446730 38446730 AGAGAGCGTCTTGTGGCTGCGGCCTGCCCCTCAGCCTCCTCCGCGCGGTTACCCCTGTACCCGCC AGAGAGCGTCTTGTGGCTGCGGCCTGCCCCTCGGCCTCCTCCGCGCGGTTACCCCTGTACCCGCC A G SNHG11 Ensembl:ENSG00000174365 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:38446691..38446839 26863196 MeRIP-seq:(Medium) rs1359062460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_831211,Human_RBP_ID_18422886 Human_miRNA_ID_2391372,Human_miRNA_ID_2592618,Human_miRNA_ID_2716584,Human_miRNA_ID_3052569,Human_miRNA_ID_3172913,Human_miRNA_ID_3172914,Human_miRNA_ID_3172915,Human_miRNA_ID_3184756,Human_miRNA_ID_3184757,Human_miRNA_ID_3184758,Human_miRNA_ID_3192070,Human_miRNA_ID_3192071,Human_miRNA_ID_3192072,Human_miRNA_ID_3192073,Human_miRNA_ID_3212255,Human_miRNA_ID_3212256,Human_miRNA_ID_3212257,Human_miRNA_ID_3212258 RMVar_hsa_circ_92452,RMVar_hsa_circ_210088 108277 RMVar_ID_108277 Human_SNP_ID_680549858 m1A Human chr20 - 38446820 38446819 38446820 CGGCCTTGGGAGGCCACCAGGGGTTCTTGGGAAGACCACTCCTCGGGCCCTGCCCCTCATTGACT CGGCCTTGGGAGGCCACCAGGGGTTCTTGGGA_GACCACTCCTCGGGCCCTGCCCCTCATTGACT CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38446712..38446851 26863196 MeRIP-seq:(Medium) rs1303306487 Functional Loss DEL dbSNP153 33..33 33 - - - 108278 RMVar_ID_108278 Human_SNP_ID_680549859 m1A Human chr20 - 38446820 38446820 38446820 CGGCCTTGGGAGGCCACCAGGGGTTCTTGGGAAGACCACTCCTCGGGCCCTGCCCCTCATTGACT CGGCCTTGGGAGGCCACCAGGGGTTCTTGGGAGGACCACTCCTCGGGCCCTGCCCCTCATTGACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:38446712..38446851 26863196 MeRIP-seq:(Medium) rs972807471 Functional Loss SNV dbSNP153 33..33 33 - - - 108279 RMVar_ID_108279 Human_SNP_ID_680557812 m1A Human chr20 + 38472924 38472924 38472924 CGTCGTCCCTTGGCGCCCTGGGAGAGTCGCTGACGGGTGGACTGACGGACCGCCTGAGGACGGCC CGTCGTCCCTTGGCGCCCTGGGAGAGTCGCTGTCGGGTGGACTGACGGACCGCCTGAGGACGGCC A T RALGAPB Ensembl:ENSG00000170471 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:38472876..38473075 26863196 MeRIP-seq:(Medium) rs1420118006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244569,Human_RBP_ID_4646521,Human_RBP_ID_5472253,Human_RBP_ID_8857382,Human_RBP_ID_9331529,Human_RBP_ID_9390617,Human_RBP_ID_18422887,Human_RBP_ID_18471252 Human_Splice_Rec_2083009 RMVar_hsa_circ_210089,RMVar_hsa_circ_83005 108280 RMVar_ID_108280 Human_SNP_ID_680669677 m1A Human chr20 + 38926468 38926468 38926468 CGCCGCCATGGCTCTGCTGTCCGAGGGCCTGGACGAGGTGCCCGCCGCCTGCCTGTCGCCGTGCG CGCCGCCATGGCTCTGCTGTCCGAGGGCCTGGGCGAGGTGCCCGCCGCCTGCCTGTCGCCGTGCG A G FAM83D Ensembl:ENSG00000101447 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:38926401..38926725 26863196 MeRIP-seq:(Medium) rs777529947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659842,Human_RBP_ID_5148426,Human_RBP_ID_9331531,Human_RBP_ID_22080661,Human_RBP_ID_22453751,Human_RBP_ID_22533643 RMVar_hsa_circ_210137,RMVar_hsa_circ_123444 108281 RMVar_ID_108281 Human_SNP_ID_680669721 m1A Human chr20 + 38926552 38926552 38926552 GCTGTTCAGCGAGTCACGGCGCCTGGCTCTGGAGGAGCTGGTGGCGGGCGGCCCCGAAGCCTTCG GCTGTTCAGCGAGTCACGGCGCCTGGCTCTGGGGGAGCTGGTGGCGGGCGGCCCCGAAGCCTTCG A G FAM83D Ensembl:ENSG00000101447 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:38926456..38926576 26863410 MeRIP-seq:(Medium) rs754613428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659842,Human_RBP_ID_9331532,Human_RBP_ID_22080662 RMVar_hsa_circ_210137,RMVar_hsa_circ_123444 108282 RMVar_ID_108282 Human_SNP_ID_680675941 m1A Human chr20 - 38952333 38952333 38952333 AGTGGAATTGCCGCTCTTTGTTCAAGTTTCTAAGTGAGTCACTCAAGTACAGTTCCAGGTGGGGG AGTGGAATTGCCGCTCTTTGTTCAAGTTTCTATGTGAGTCACTCAAGTACAGTTCCAGGTGGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:38952283..38952550 26863196 MeRIP-seq:(Medium) rs1424361932 Functional Loss SNV dbSNP153 33..33 33 - - - 108283 RMVar_ID_108283 Human_SNP_ID_680678346 m1A Human chr20 - 38962095 38962095 38962095 GCTCCTCCGCCTACCTCTTGAGCGTGGAGGGTAGATGCTTCAGGTGACCTTTTACGAGCGTGGCG GCTCCTCCGCCTACCTCTTGAGCGTGGAGGGTGGATGCTTCAGGTGACCTTTTACGAGCGTGGCG T C AL023803.1 Ensembl:ENSG00000261431 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:38961980..38962126 26863196 MeRIP-seq:(Medium) rs1481228988 Functional Loss SNV dbSNP153 33..33 33 - - - 108284 RMVar_ID_108284 Human_SNP_ID_680687018 m1A Human chr20 + 38997748 38997748 38997748 TCCGTGTGTGAGGGGCCTACGTGAGGTATGGGATGTGAGTTCGTATGTGAGTGAAAGAAAGAAAG TCCGTGTGTGAGGGGCCTACGTGAGGTATGGGGTGTGAGTTCGTATGTGAGTGAAAGAAAGAAAG A G DHX35 Ensembl:ENSG00000101452 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:38997710..38997783 26863196 MeRIP-seq:(Medium) rs1031875125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23904873 RMVar_hsa_circ_101465,RMVar_hsa_circ_49605,RMVar_hsa_circ_210141,RMVar_hsa_circ_210145,RMVar_hsa_circ_333227,RMVar_hsa_circ_346013,RMVar_hsa_circ_46457 108285 RMVar_ID_108285 Human_SNP_ID_282855310 m1A Human chr6 + 75119177 75119177 75119177 CCCAAGTCAAGACTTTCTCCTTGATAAACGTGAGGGCCTTGCCTACAGAATGTGGCATGGAAAAT CCCAAGTCAAGACTTTCTCCTTGATAAACGTGGGGGCCTTGCCTACAGAATGTGGCATGGAAAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75119126..75119200 26863196 MeRIP-seq:(Medium) rs550232635 Functional Loss SNV dbSNP153 33..33 33 - - - 108286 RMVar_ID_108286 Human_SNP_ID_282861425 m1A Human chr6 + 75144104 75144104 75144104 CTCTAGCTCCACTTCCACATTTCTGCGCCTCCATCTCTTCAACATTTTTATCTTGTGTATCTCTC CTCTAGCTCCACTTCCACATTTCTGCGCCTCCGTCTCTTCAACATTTTTATCTTGTGTATCTCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75144078..75144253 26863196 MeRIP-seq:(Medium) rs1038229172 Functional Loss SNV dbSNP153 33..33 33 - - - 108287 RMVar_ID_108287 Human_SNP_ID_282876538 m1A Human chr6 - 75205881 75205881 75205881 GCCTCGGCGGCCGCCAGGTGCTCCTGGAGTGCAGCGCCTATCGCCGGGGCGTGTGGGGGCCACAC GCCTCGGCGGCCGCCAGGTGCTCCTGGAGTGCGGCGCCTATCGCCGGGGCGTGTGGGGGCCACAC T C COL12A1 Ensembl:ENSG00000111799 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:75205831..75205997 26863196 MeRIP-seq:(Medium) rs565301271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4897496 108288 RMVar_ID_108288 Human_SNP_ID_282876540 m1A Human chr6 + 75205892 75205892 75205892 ACACGCCCCGGCGATAGGCGCTGCACTCCAGGAGCACCTGGCGGCCGCCGAGGCGTGGGCAGCTG ACACGCCCCGGCGATAGGCGCTGCACTCCAGGGGCACCTGGCGGCCGCCGAGGCGTGGGCAGCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:75205843..75205992 26863196 MeRIP-seq:(Medium) rs1278297902 Functional Loss SNV dbSNP153 33..33 33 - - - 108289 RMVar_ID_108289 Human_SNP_ID_282884103 m1A Human chr6 + 75237950 75237950 75237950 GGATGACTGAAGTCACTCCTGCTTCTTGGGAAATGAAGCCACAGCCAGCTCATATATGGCATATG GGATGACTGAAGTCACTCCTGCTTCTTGGGAAGTGAAGCCACAGCCAGCTCATATATGGCATATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:75237901..75238000 32194978 MeRIP-seq:(Medium) rs752963398 Functional Loss SNV dbSNP153 33..33 33 - - - 108290 RMVar_ID_108290 Human_SNP_ID_282885701 m1A Human chr6 - 75243747 75243744 75243748 TTGGTGGTGTTCAGTTGTGGCGGTTGCTGGTCAGTAACAGCCAAGATGCTGCGGAATCTGCTGGT TTGGTGGTGTTCAGTTGTGGCGGTTGCTGGT____AACAGCCAAGATGCTGCGGAATCTGCTGGT TACTG T COX7A2 Ensembl:ENSG00000112695 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:75243701..75243800 26863196 MeRIP-seq:(Medium) rs1562373235 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_252088,Human_RBP_ID_668070,Human_RBP_ID_1675996,Human_RBP_ID_4903422,Human_RBP_ID_5122057,Human_RBP_ID_5151948,Human_RBP_ID_5327190,Human_RBP_ID_9198338,Human_RBP_ID_9336224,Human_RBP_ID_17663807,Human_RBP_ID_18425854,Human_RBP_ID_22460779,Human_RBP_ID_23214890,Human_RBP_ID_24171405 Human_Splice_Rec_787847,Human_Splice_Rec_787853,Human_Splice_Rec_787859,Human_Splice_Rec_787865,Human_Splice_Rec_787871,Human_Splice_Rec_787875,Human_Splice_Rec_787879,Human_Splice_Rec_787883 108291 RMVar_ID_108291 Human_SNP_ID_282885704 m1A Human chr6 - 75243747 75243747 75243747 TTGGTGGTGTTCAGTTGTGGCGGTTGCTGGTCAGTAACAGCCAAGATGCTGCGGAATCTGCTGGT TTGGTGGTGTTCAGTTGTGGCGGTTGCTGGTCGGTAACAGCCAAGATGCTGCGGAATCTGCTGGT T C COX7A2 Ensembl:ENSG00000112695 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:75243701..75243800 26863196 MeRIP-seq:(Medium) rs201500909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252088,Human_RBP_ID_668070,Human_RBP_ID_1675996,Human_RBP_ID_4903422,Human_RBP_ID_5122057,Human_RBP_ID_5151948,Human_RBP_ID_5327190,Human_RBP_ID_9198338,Human_RBP_ID_9336224,Human_RBP_ID_17663807,Human_RBP_ID_18425854,Human_RBP_ID_22460779,Human_RBP_ID_23214890,Human_RBP_ID_24171405 Human_Splice_Rec_787847,Human_Splice_Rec_787853,Human_Splice_Rec_787859,Human_Splice_Rec_787865,Human_Splice_Rec_787871,Human_Splice_Rec_787875,Human_Splice_Rec_787879,Human_Splice_Rec_787883 108292 RMVar_ID_108292 Human_SNP_ID_282885718 m1A Human chr6 + 75243762 75243762 75243762 AGCATCTTGGCTGTTACTGACCAGCAACCGCCACAACTGAACACCACCAACGAAAATGGCCACGC AGCATCTTGGCTGTTACTGACCAGCAACCGCCGCAACTGAACACCACCAACGAAAATGGCCACGC A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75243657..75243800 26863196 MeRIP-seq:(Medium) rs766079388 Functional Loss SNV dbSNP153 33..33 33 - - - 108293 RMVar_ID_108293 Human_SNP_ID_282885720 m1A Human chr6 + 75243765 75243765 75243765 ATCTTGGCTGTTACTGACCAGCAACCGCCACAACTGAACACCACCAACGAAAATGGCCACGCCGG ATCTTGGCTGTTACTGACCAGCAACCGCCACAGCTGAACACCACCAACGAAAATGGCCACGCCGG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:75243653..75243800 26863196 MeRIP-seq:(Medium) rs751303561 Functional Loss SNV dbSNP153 33..33 33 - - - 108294 RMVar_ID_108294 Human_SNP_ID_282885722 m1A Human chr6 - 75243767 75243767 75243767 TTCCGGCGTGGCCATTTTCGTTGGTGGTGTTCAGTTGTGGCGGTTGCTGGTCAGTAACAGCCAAG TTCCGGCGTGGCCATTTTCGTTGGTGGTGTTCGGTTGTGGCGGTTGCTGGTCAGTAACAGCCAAG T C COX7A2 Ensembl:ENSG00000112695 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:75243665..75243800 26863196 MeRIP-seq:(Medium) rs1417593361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81532,Human_RBP_ID_668070,Human_RBP_ID_4903422,Human_RBP_ID_5122057,Human_RBP_ID_5151948,Human_RBP_ID_5327190,Human_RBP_ID_9198338,Human_RBP_ID_9336224,Human_RBP_ID_17663807,Human_RBP_ID_18425854,Human_RBP_ID_22460779,Human_RBP_ID_23214890,Human_RBP_ID_24171406 Human_Splice_Rec_787847,Human_Splice_Rec_787853,Human_Splice_Rec_787859,Human_Splice_Rec_787865,Human_Splice_Rec_787871,Human_Splice_Rec_787875,Human_Splice_Rec_787879,Human_Splice_Rec_787883 108295 RMVar_ID_108295 Human_SNP_ID_282894804 m1A Human chr6 - 75284646 75284646 75284646 TGGTCCACCTGCAAATCGCGGAGCGGCGCCCCAGGGATCGATGGCGATGAACTATAACGCGAAGG TGGTCCACCTGCAAATCGCGGAGCGGCGCCCCGGGGATCGATGGCGATGAACTATAACGCGAAGG T C TMEM30A Ensembl:ENSG00000112697 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:75284554..75284775 26863196 MeRIP-seq:(Medium) rs1356569344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79768,Human_RBP_ID_842072,Human_RBP_ID_1676075,Human_RBP_ID_2026222,Human_RBP_ID_4903424,Human_RBP_ID_7628106,Human_RBP_ID_8905856,Human_RBP_ID_8944025,Human_RBP_ID_15877592,Human_RBP_ID_18869211,Human_RBP_ID_22106064 RMVar_hsa_circ_77233,RMVar_hsa_circ_239626 108296 RMVar_ID_108296 Human_SNP_ID_282894847 m1A Human chr6 - 75284727 75284727 75284727 GTGGCGCTGGTGGCTGCGGCGGCGGCGGCGGCAGCGGCGCTCGAGCGGTTCCTGTCAGGGTCAGC GTGGCGCTGGTGGCTGCGGCGGCGGCGGCGGCCGCGGCGCTCGAGCGGTTCCTGTCAGGGTCAGC T G TMEM30A Ensembl:ENSG00000112697 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:75284509..75284775 26863196 MeRIP-seq:(Medium) rs1405164080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_79768,Human_RBP_ID_789962,Human_RBP_ID_841733,Human_RBP_ID_4903426,Human_RBP_ID_5327502,Human_RBP_ID_8905857,Human_RBP_ID_9336225,Human_RBP_ID_22460780,Human_RBP_ID_24554658 Human_miRNA_ID_2442864 RMVar_hsa_circ_77233,RMVar_hsa_circ_239626 108297 RMVar_ID_108297 Human_SNP_ID_282966586 m1A Human chr6 - 75602012 75602012 75602012 GGCCCCTAGCTCGTTCTGCAGCCGCCGCCGCTACGGCCGTCCGCCCACCCCGCCCAGGCGTGAAT GGCCCCTAGCTCGTTCTGCAGCCGCCGCCGCTGCGGCCGTCCGCCCACCCCGCCCAGGCGTGAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:75601876..75602238;chr6:75601757..75621582 26863196 MeRIP-seq:(Medium) rs915917776 Functional Loss SNV dbSNP153 33..33 33 - - - 108298 RMVar_ID_108298 Human_SNP_ID_283016845 m1A Human chr6 + 75801388 75801388 75801388 GAGAGGAGGGGTGGTTGTTCTTGCATGGCTTAAGAAGGAATAGGATCTGGTGGGTGAGTAGCGAC GAGAGGAGGGGTGGTTGTTCTTGCATGGCTTAGGAAGGAATAGGATCTGGTGGGTGAGTAGCGAC A G MYO6 Ensembl:ENSG00000196586 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:75801371..75801484 26863196 MeRIP-seq:(Medium) rs1243834067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10297546 108299 RMVar_ID_108299 Human_SNP_ID_283020739 m1A Human chr6 - 75817397 75817393 75817397 TTCAAAAGTTCACATGTAAGTCCCAACTAACAAACACATCTGCCCATGCCACATAAAATCCCCAC TTCAAAAGTTCACATGTAAGTCCCAACTAACA____CATCTGCCCATGCCACATAAAATCCCCAC GTGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:75817385..75817512 26863196 MeRIP-seq:(Medium) rs1306472093 Functional Loss DEL dbSNP153 33..36 33 - - - 108300 RMVar_ID_108300 Human_SNP_ID_283020746 m1A Human chr6 + 75817438 75817438 75817438 GGGACTTACATGTGAACTTTTGAAAAAGATACATTATTTGTTTTATATATATTTCAAAACTGATT GGGACTTACATGTGAACTTTTGAAAAAGATACGTTATTTGTTTTATATATATTTCAAAACTGATT A G MYO6 Ensembl:ENSG00000196586 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75817434..75817562 26863196 MeRIP-seq:(Medium) rs536989771 Functional Loss SNV dbSNP153 33..33 33 - - - 108301 RMVar_ID_108301 Human_SNP_ID_283037612 m1A Human chr6 + 75890149 75890149 75890149 GAGGAACTCCTCAGTGCATTACAGAAAAAAAAACAGCAGGAAGAGGAAGCAGAAAGGCTGAGGCG GAGGAACTCCTCAGTGCATTACAGAAAAAAAAGCAGCAGGAAGAGGAAGCAGAAAGGCTGAGGCG A G MYO6 Ensembl:ENSG00000196586 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:75890145..75890274 26863196 MeRIP-seq:(Medium) rs776905500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_788340,Human_Splice_Rec_788408,Human_Splice_Rec_788458,Human_Splice_Rec_788512,Human_Splice_Rec_788564,Human_Splice_Rec_788628,Human_Splice_Rec_788678,Human_Splice_Rec_788742,Human_Splice_Rec_788794,Human_Splice_Rec_788858,Human_Splice_Rec_788926,Human_Splice_Rec_788998,Human_Splice_Rec_789144,Human_Splice_Rec_789208,Human_Splice_Rec_789256 RMVar_hsa_circ_34420,RMVar_hsa_circ_28547,RMVar_hsa_circ_45882,RMVar_hsa_circ_21587,RMVar_hsa_circ_74139,RMVar_hsa_circ_73058,RMVar_hsa_circ_363637,RMVar_hsa_circ_68255,RMVar_hsa_circ_71770,RMVar_hsa_circ_51102,RMVar_hsa_circ_68568 108302 RMVar_ID_108302 Human_SNP_ID_283037626 m1A Human chr6 + 75890193 75890193 75890193 GGAAGCAGAAAGGCTGAGGCGTATTCAAGAAGAAATGGAAAAGGAAAGAAAAAGACGTGAAGAAG GGAAGCAGAAAGGCTGAGGCGTATTCAAGAAGCAATGGAAAAGGAAAGAAAAAGACGTGAAGAAG A C MYO6 Ensembl:ENSG00000196586 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:75890143..75890312 26863196 MeRIP-seq:(Medium) rs1191940227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81905,Human_RBP_ID_4897889,Human_RBP_ID_24171952,Human_RBP_ID_24548427,Human_RBP_ID_26355346 Human_Splice_Rec_788341,Human_Splice_Rec_788565,Human_Splice_Rec_788679,Human_Splice_Rec_788743,Human_Splice_Rec_788795,Human_Splice_Rec_788859,Human_Splice_Rec_788927,Human_Splice_Rec_789145,Human_Splice_Rec_789257,Human_Splice_Rec_789275 RMVar_hsa_circ_34420,RMVar_hsa_circ_28547,RMVar_hsa_circ_45882,RMVar_hsa_circ_21587,RMVar_hsa_circ_74139,RMVar_hsa_circ_73058,RMVar_hsa_circ_363637,RMVar_hsa_circ_68255,RMVar_hsa_circ_71770,RMVar_hsa_circ_51102,RMVar_hsa_circ_68568 108303 RMVar_ID_108303 Human_SNP_ID_283037659 m1A Human chr6 + 75890257 75890257 75890257 GACGAAAAACGTCGAAGAAAGGAAGAGGAGGAAAGGCGGATGTGAGGCATTTATATTATTTTGAA GACGAAAAACGTCGAAGAAAGGAAGAGGAGGAGAGGCGGATGTGAGGCATTTATATTATTTTGAA A G MYO6 Ensembl:ENSG00000196586 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75890115..75890337 26863196 MeRIP-seq:(Medium) rs1249635121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252440,Human_RBP_ID_3970294,Human_RBP_ID_24548427,Human_RBP_ID_26354160,Human_RBP_ID_27827810 Human_Splice_Rec_788341,Human_Splice_Rec_788565,Human_Splice_Rec_788679,Human_Splice_Rec_788743,Human_Splice_Rec_788795,Human_Splice_Rec_788859,Human_Splice_Rec_788927,Human_Splice_Rec_789145,Human_Splice_Rec_789257,Human_Splice_Rec_789275 RMVar_hsa_circ_34420,RMVar_hsa_circ_28547,RMVar_hsa_circ_45882,RMVar_hsa_circ_21587,RMVar_hsa_circ_74139,RMVar_hsa_circ_73058,RMVar_hsa_circ_363637,RMVar_hsa_circ_68255,RMVar_hsa_circ_71770,RMVar_hsa_circ_51102,RMVar_hsa_circ_68568 108304 RMVar_ID_108304 Human_SNP_ID_283037873 m1A Human chr6 - 75891160 75891156 75891160 AGAAAATAAAGAATCCTTCAGAAGGCAATTTAACTATTATTTAATAATAAACAAAGGTAACAGAT AGAAAATAAAGAATCCTTCAGAAGGCAATTTA____TTATTTAATAATAAACAAAGGTAACAGAT ATAGT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:75891158..75891365 26863196 MeRIP-seq:(Medium) rs1248134057 Functional Loss DEL dbSNP153 33..36 33 - - - 108305 RMVar_ID_108305 Human_SNP_ID_283408296 m1A Human chr6 - 77258828 77258827 77258829 GAGAGAGGAAGGAAGGAAGGAAAGAGAGAGAAAGAAAGAGAGGAAGGAAGGAAGGAGAAAGAAAA GAGAGAGGAAGGAAGGAAGGAAAGAGAGAGA__GAAAGAGAGGAAGGAAGGAAGGAGAAAGAAAA CTT C lnc-HTR1B-1,lnc-HTR1B-1:2,lnc-HTR1B-1:3,lnc-HTR1B-1:4,lnc-HTR1B-1:5,lnc-HTR1B-1:6 RNACentral:URS0000D5C28A,RNACentral:URS0000D573A8,RNACentral:URS0000D595B1,RNACentral:URS0000D5CA56,RNACentral:URS0000D5BB43,RNACentral:URS0000D5742D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:77258780..77258872 26863196 MeRIP-seq:(Medium) rs954637061 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_239716 108306 RMVar_ID_108306 Human_SNP_ID_283877831 m1A Human chr6 + 79064252 79064252 79064252 ATTCTAGTATGTACACTAACTTCCTCTCAACCAACTCCTTCCCATCTACATGTAAACATGCTCAT ATTCTAGTATGTACACTAACTTCCTCTCAACCGACTCCTTCCCATCTACATGTAAACATGCTCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:79064249..79064446 26863196 MeRIP-seq:(Medium) rs1326053818 Functional Loss SNV dbSNP153 33..33 33 - - - 108307 RMVar_ID_108307 Human_SNP_ID_283877845 m1A Human chr6 - 79064325 79064325 79064325 GATATTTGGGTGGGGAGGTGTTGGATAATAGCAGTTAGGCAGGATTTTTGTTTTTTCCTAAAGTG GATATTTGGGTGGGGAGGTGTTGGATAATAGCTGTTAGGCAGGATTTTTGTTTTTTCCTAAAGTG T A PHIP Ensembl:ENSG00000146247 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:79064276..79064449 26863196 MeRIP-seq:(Medium) rs1562220649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7631726 RMVar_hsa_circ_104838,RMVar_hsa_circ_239727,RMVar_hsa_circ_5281,RMVar_hsa_circ_4575,RMVar_hsa_circ_372446,RMVar_hsa_circ_239770 108308 RMVar_ID_108308 Human_SNP_ID_283881123 m1A Human chr6 + 79077265 79077265 79077265 CAAATAAATTGTCCGCAGCCCCTGCGGCCCCGAAGTACGAGTACCCCCGGCCACTGGCCCCCGCA CAAATAAATTGTCCGCAGCCCCTGCGGCCCCGGAGTACGAGTACCCCCGGCCACTGGCCCCCGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:79077216..79077300 26863196 MeRIP-seq:(Medium) rs372741754 Functional Loss SNV dbSNP153 33..33 33 - - - 108309 RMVar_ID_108309 Human_SNP_ID_283910842 m1A Human chr6 + 79201639 79201639 79201639 TTTACAAAATACTTGGTAAAAATAGCTTTTAAAAGTTGTCCCAAGAGATACATAAAATCAACCCC TTTACAAAATACTTGGTAAAAATAGCTTTTAAGAGTTGTCCCAAGAGATACATAAAATCAACCCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:79201485..79201679 32194978 MeRIP-seq:(Medium) rs1205012522 Functional Loss SNV dbSNP153 33..33 33 - - - 108310 RMVar_ID_108310 Human_SNP_ID_283918543 m1A Human chr6 + 79234354 79234354 79234354 GTCACTGGAGAGAAAGTAACATTAAGAGATCGATGAGGACGGAGTGGGTAGGGGGGACAGAGAGA GTCACTGGAGAGAAAGTAACATTAAGAGATCGCTGAGGACGGAGTGGGTAGGGGGGACAGAGAGA A C HMGN3-AS1 Ensembl:ENSG00000270362 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:79234350..79234451 26863196 MeRIP-seq:(Medium) rs769856162 Functional Loss SNV dbSNP153 33..33 33 - - - 108311 RMVar_ID_108311 Human_SNP_ID_283918640 m1A Human chr6 + 79234594 79234594 79234594 ATGACTATGTCGGTGAAGCAAAAAGTAAAGCAACGGACTGGAACTGCTGGCGCCGCCGCTGGATG ATGACTATGTCGGTGAAGCAAAAAGTAAAGCAGCGGACTGGAACTGCTGGCGCCGCCGCTGGATG A G HMGN3-AS1 Ensembl:ENSG00000270362 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:79215021..79234850;chr6:79234519..79234795;chr6:79234495..79234800 26863196 MeRIP-seq:(Medium) rs748966009 Functional Loss SNV dbSNP153 33..33 33 - - - 108312 RMVar_ID_108312 Human_SNP_ID_283918659 m1A Human chr6 - 79234638 79234638 79234638 CTACGTCGTGCCCTGCGCGTGAGCAGCTGCAGAGGCAGAGGCAGCATCCAGCGGCGGCGCCAGCA CTACGTCGTGCCCTGCGCGTGAGCAGCTGCAGCGGCAGAGGCAGCATCCAGCGGCGGCGCCAGCA T G HMGN3 Ensembl:ENSG00000118418 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9361504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4898641 Human_Splice_Rec_789545,Human_Splice_Rec_789555,Human_Splice_Rec_789565 108313 RMVar_ID_108313 Human_SNP_ID_283999990 m1A Human chr6 + 79560117 79560117 79560117 GGAAGGGAATCAATGTTGGGGGTGGGGAGCATACACCATTCTGGGAAACTGAGGGGACCAAAACC GGAAGGGAATCAATGTTGGGGGTGGGGAGCATTCACCATTCTGGGAAACTGAGGGGACCAAAACC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:79560001..79560132 26863196 MeRIP-seq:(Medium) rs1486519756 Functional Loss SNV dbSNP153 33..33 33 - - - 108314 RMVar_ID_108314 Human_SNP_ID_284131324 m1A Human chr6 + 80106726 80106725 80106727 ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCTACTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCT__TCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA TAC T BCKDHB Ensembl:ENSG00000083123 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:80106676..80106900 26863196 MeRIP-seq:(Medium) rs398124572 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1972679,Human_miRNA_ID_1974856,Human_miRNA_ID_2612672 Clinvar_Rec_700 RMVar_hsa_circ_88367,RMVar_hsa_circ_239792 108315 RMVar_ID_108315 Human_SNP_ID_284131325 m1A Human chr6 - 80106725 80106725 80106725 GCCCCTCAGCCCCTGCCGCCCTGAGCCTGAGTAGCCAGCCGGCAGCCGCCGCTACAACCGCCATC GCCCCTCAGCCCCTGCCGCCCTGAGCCTGAGTGGCCAGCCGGCAGCCGCCGCTACAACCGCCATC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:80106676..80127274 26863196 MeRIP-seq:(Medium) rs1156405002 Functional Loss SNV dbSNP153 33..33 33 - - - 108316 RMVar_ID_108316 Human_SNP_ID_284131326 m1A Human chr6 + 80106726 80106726 80106726 ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCTACTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCTGCTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA A G BCKDHB Ensembl:ENSG00000083123 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:80106676..80106900 26863196 MeRIP-seq:(Medium) rs755140913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1972679,Human_miRNA_ID_1974856,Human_miRNA_ID_2612672 RMVar_hsa_circ_88367,RMVar_hsa_circ_239792 108317 RMVar_ID_108317 Human_SNP_ID_284131327 m1A Human chr6 + 80106726 80106726 80106726 ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCTACTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA ATGGCGGTTGTAGCGGCGGCTGCCGGCTGGCTTCTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCA A T BCKDHB Ensembl:ENSG00000083123 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:80106676..80106900 26863196 MeRIP-seq:(Medium) rs755140913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1972679,Human_miRNA_ID_1974856,Human_miRNA_ID_2612672 RMVar_hsa_circ_88367,RMVar_hsa_circ_239792 108318 RMVar_ID_108318 Human_SNP_ID_284131332 m1A Human chr6 + 80106736 80106736 80106736 TAGCGGCGGCTGCCGGCTGGCTACTCAGGCTCAGGGCGGCAGGGGCTGAGGGGCACTGGCGTCGG TAGCGGCGGCTGCCGGCTGGCTACTCAGGCTCCGGGCGGCAGGGGCTGAGGGGCACTGGCGTCGG A C BCKDHB Ensembl:ENSG00000083123 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:80106686..80106838;chr6:80106690..80106845 26863196 MeRIP-seq:(Medium) rs781373417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1972679,Human_miRNA_ID_1974856,Human_miRNA_ID_2612672 RMVar_hsa_circ_88367,RMVar_hsa_circ_239792 108319 RMVar_ID_108319 Human_SNP_ID_284191453 m1A Human chr6 - 80357227 80357227 80357227 CTCCTCCTTGCTCCTTCAGGCAAGGGAATGGTAATGACTTCCCACAGTTGCTAGTTCCTGGGTGC CTCCTCCTTGCTCCTTCAGGCAAGGGAATGGTTATGACTTCCCACAGTTGCTAGTTCCTGGGTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:80357187..80357252 26863196 MeRIP-seq:(Medium) rs1399320930 Functional Loss SNV dbSNP153 33..33 33 - - - 108320 RMVar_ID_108320 Human_SNP_ID_284682930 m1A Human chr6 + 82170990 82170990 82170990 AAACACAAAATTCTGGCCATTAATGAATCAGAAGTAATAACTGATGCTCCTACTTTAAATTCATC AAACACAAAATTCTGGCCATTAATGAATCAGACGTAATAACTGATGCTCCTACTTTAAATTCATC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:82170944..82171030 32194978 MeRIP-seq:(Medium) rs547598869 Functional Loss SNV dbSNP153 33..33 33 - - - 108321 RMVar_ID_108321 Human_SNP_ID_284732171 m1A Human chr6 + 82364298 82364298 82364298 GAGGCGGTGCAGGAAGGAACGGGAGAGGGAGAAGTTTGGTAGGGAAGGAATTGGGGATTAAGCGG GAGGCGGTGCAGGAAGGAACGGGAGAGGGAGAGGTTTGGTAGGGAAGGAATTGGGGATTAAGCGG A G TPBG Ensembl:ENSG00000146242 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:82364265..82364407 26863196 MeRIP-seq:(Medium) rs1263588329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_790451 108322 RMVar_ID_108322 Human_SNP_ID_284732296 m1A Human chr6 + 82364673 82364673 82364673 CGAGGGGCGCCAACAAGAGGCGAAGAGGTGGCACCAGGGCGGCGGCAGGAAGAGGAGCGGGAGCA CGAGGGGCGCCAACAAGAGGCGAAGAGGTGGCGCCAGGGCGGCGGCAGGAAGAGGAGCGGGAGCA A G TPBG Ensembl:ENSG00000146242 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:82364601..82364749 26863196 MeRIP-seq:(Medium) rs1283400153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_790448,Human_Splice_Rec_790450,Human_Splice_Rec_790452 108323 RMVar_ID_108323 Human_SNP_ID_284732499 m1A Human chr6 + 82365064 82365064 82365064 TACTCCTGGGCTGGGTCTCCTCGTCTTCTCCCACCTCCTCGGCATCCTCCTTCTCCTCCTCGGCG TACTCCTGGGCTGGGTCTCCTCGTCTTCTCCCGCCTCCTCGGCATCCTCCTTCTCCTCCTCGGCG A G TPBG Ensembl:ENSG00000146242 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:82365014..82365235 26863196 MeRIP-seq:(Medium) rs1398611549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5451495,Human_RBP_ID_5512054,Human_RBP_ID_27101206,Human_RBP_ID_27526208 108324 RMVar_ID_108324 Human_SNP_ID_284732502 m1A Human chr6 - 82365067 82365067 82365067 CGGCGCCGAGGAGGAGAAGGAGGATGCCGAGGAGGTGGGAGAAGACGAGGAGACCCAGCCCAGGA CGGCGCCGAGGAGGAGAAGGAGGATGCCGAGGTGGTGGGAGAAGACGAGGAGACCCAGCCCAGGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:82364917..82365067 32194978 MeRIP-seq:(Medium) rs1369072903 Functional Loss SNV dbSNP153 33..33 33 - - - 108325 RMVar_ID_108325 Human_SNP_ID_284732549 m1A Human chr6 + 82365125 82365125 82365125 GGCGCCGTTCCTGGCTTCCGCCGTGTCCGCCCAGCCCCCGCTGCCGGACCAGTGCCCCGCGCTGT GGCGCCGTTCCTGGCTTCCGCCGTGTCCGCCCGGCCCCCGCTGCCGGACCAGTGCCCCGCGCTGT A G TPBG Ensembl:ENSG00000146242 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:82365032..82365250 26863196 MeRIP-seq:(Medium) rs1384674021 Functional Loss SNV dbSNP153 33..33 33 - - - 108326 RMVar_ID_108326 Human_SNP_ID_284890076 m1A Human chr6 - 82999988 82999988 82999988 AGAGGCTAAGGGAGGAAACTGCTTTAAGAAGGAGAAAGTAGTCAAACGCTGCTGAGAGAGAGGTC AGAGGCTAAGGGAGGAAACTGCTTTAAGAAGGGGAAAGTAGTCAAACGCTGCTGAGAGAGAGGTC T C UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:82999957..83000044 26863196 MeRIP-seq:(Medium) rs937079379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15891414 RMVar_hsa_circ_239851,RMVar_hsa_circ_272079,RMVar_hsa_circ_288773,RMVar_hsa_circ_300012,RMVar_hsa_circ_304717,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_41154,RMVar_hsa_circ_107017,RMVar_hsa_circ_239853,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_239852 108327 RMVar_ID_108327 Human_SNP_ID_284900638 m1A Human chr6 + 83044548 83044548 83044548 ACCAAGAAGAAAGAGTCTCCAATAAAACAGTCATTCTCTTGCGGATGAAGTGATTTATTAGCAAA ACCAAGAAGAAAGAGTCTCCAATAAAACAGTCGTTCTCTTGCGGATGAAGTGATTTATTAGCAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:83044500..83044578 32194978 MeRIP-seq:(Medium) rs1196387863 Functional Loss SNV dbSNP153 33..33 33 - - - 108328 RMVar_ID_108328 Human_SNP_ID_284905693 m1A Human chr6 + 83065722 83065721 83065722 ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGCAGGCTTCCAGTCCCAGACCGGACCAAGCTGGAG ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGC_GGCTTCCAGTCCCAGACCGGACCAAGCTGGAG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83065627..83065776 26863196 MeRIP-seq:(Medium) rs777020213 Functional Loss DEL dbSNP153 33..33 33 - - - 108329 RMVar_ID_108329 Human_SNP_ID_284905696 m1A Human chr6 + 83065722 83065722 83065722 ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGCAGGCTTCCAGTCCCAGACCGGACCAAGCTGGAG ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGCCGGCTTCCAGTCCCAGACCGGACCAAGCTGGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83065627..83065776 26863196 MeRIP-seq:(Medium) rs754581808 Functional Loss SNV dbSNP153 33..33 33 - - - 108330 RMVar_ID_108330 Human_SNP_ID_284905697 m1A Human chr6 + 83065722 83065722 83065722 ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGCAGGCTTCCAGTCCCAGACCGGACCAAGCTGGAG ACGCGCGTCTCCGCCGCAGAAGCCGCCATGGCGGGCTTCCAGTCCCAGACCGGACCAAGCTGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83065627..83065776 26863196 MeRIP-seq:(Medium) rs754581808 Functional Loss SNV dbSNP153 33..33 33 - - - 108331 RMVar_ID_108331 Human_SNP_ID_284905704 m1A Human chr6 + 83065736 83065736 83065736 CGCAGAAGCCGCCATGGCAGGCTTCCAGTCCCAGACCGGACCAAGCTGGAGGTTCCGAGGGGCCC CGCAGAAGCCGCCATGGCAGGCTTCCAGTCCCTGACCGGACCAAGCTGGAGGTTCCGAGGGGCCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:83065687..83065762 26863196 MeRIP-seq:(Medium) rs989728659 Functional Loss SNV dbSNP153 33..33 33 - - - 108332 RMVar_ID_108332 Human_SNP_ID_284906281 m1A Human chr6 + 83067760 83067760 83067760 CCGTGGTTGCCAGGAGAGCTGCGCCGGCGAGAAGCGGCCGAGCCAGCAGCAGGTAAAAGCGTCCC CCGTGGTTGCCAGGAGAGCTGCGCCGGCGAGAGGCGGCCGAGCCAGCAGCAGGTAAAAGCGTCCC A G DOP1A Ensembl:ENSG00000083097 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83067716..83067800 26863196 MeRIP-seq:(Medium) rs1474166774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18425462 Human_Splice_Rec_790555,Human_Splice_Rec_790633 RMVar_hsa_circ_239863,RMVar_hsa_circ_94981 108333 RMVar_ID_108333 Human_SNP_ID_284906371 m1A Human chr6 - 83067955 83067955 83067955 GTCCCCGCGCAGCTCCCGACTCCCCGTAAACCAGAGGGCGGCCGACCAGCTTCGCAGCTCCTGGC GTCCCCGCGCAGCTCCCGACTCCCCGTAAACCTGAGGGCGGCCGACCAGCTTCGCAGCTCCTGGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:83067849..83068074 26863196 MeRIP-seq:(Medium) rs1338865965 Functional Loss SNV dbSNP153 33..33 33 - - - 108334 RMVar_ID_108334 Human_SNP_ID_284906402 m1A Human chr6 - 83068015 83068015 83068015 CCTGGGGCCGCCCTCGCGCCTCTGCCCGGCCCAGGCCCCGGCCCCAGCCCTGGCCCTCCAGTCCC CCTGGGGCCGCCCTCGCGCCTCTGCCCGGCCCGGGCCCCGGCCCCAGCCCTGGCCCTCCAGTCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:83067965..83068084 26863196 MeRIP-seq:(Medium) rs979073684 Functional Loss SNV dbSNP153 33..33 33 - - - 108335 RMVar_ID_108335 Human_SNP_ID_284906403 m1A Human chr6 - 83068015 83068015 83068015 CCTGGGGCCGCCCTCGCGCCTCTGCCCGGCCCAGGCCCCGGCCCCAGCCCTGGCCCTCCAGTCCC CCTGGGGCCGCCCTCGCGCCTCTGCCCGGCCCCGGCCCCGGCCCCAGCCCTGGCCCTCCAGTCCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:83067965..83068084 26863196 MeRIP-seq:(Medium) rs979073684 Functional Loss SNV dbSNP153 33..33 33 - - - 108336 RMVar_ID_108336 Human_SNP_ID_284930023 m1A Human chr6 + 83167146 83167146 83167146 TCACATACCTTCTCATTTGACTTCTCTACTAAAAGGTAGTTTTAGACTGTCCCATTTTATAAGTG TCACATACCTTCTCATTTGACTTCTCTACTAAGAGGTAGTTTTAGACTGTCCCATTTTATAAGTG A G DOP1A Ensembl:ENSG00000083097 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:83167097..83167245 32194978 MeRIP-seq:(Medium) rs1185677463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121951,RMVar_hsa_circ_239891 108337 RMVar_ID_108337 Human_SNP_ID_284936369 m1A Human chr6 + 83193226 83193226 83193226 CCCTTCACCTACACGCAGCGGAGAAGCGCCCAAGCAACAACGTCTGCACCCAAACCCAGTCCTCA CCCTTCACCTACACGCAGCGGAGAAGCGCCCAGGCAACAACGTCTGCACCCAAACCCAGTCCTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83192847..83193240 26863196 MeRIP-seq:(Medium) rs1397127507 Functional Loss SNV dbSNP153 33..33 33 - - - 108338 RMVar_ID_108338 Human_SNP_ID_284974740 m1A Human chr6 - 83354022 83354022 83354022 TTAAGAAGACAGAGAGGAGGAGGAGGCAGCAAAGGAACCTGAGAAGAAGCAGGTAGTGATTAGGA TTAAGAAGACAGAGAGGAGGAGGAGGCAGCAAGGGAACCTGAGAAGAAGCAGGTAGTGATTAGGA T C ME1 Ensembl:ENSG00000065833 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83354018..83354083 26863196 MeRIP-seq:(Medium) rs1288150013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91621,RMVar_hsa_circ_239910,RMVar_hsa_circ_369203,RMVar_hsa_circ_118786,RMVar_hsa_circ_239914,RMVar_hsa_circ_341049,RMVar_hsa_circ_239916,RMVar_hsa_circ_239918,RMVar_hsa_circ_289967,RMVar_hsa_circ_239919 108339 RMVar_ID_108339 Human_SNP_ID_284983152 m1A Human chr6 - 83391681 83391681 83391681 TGAGAGAGAGGGAGAGTAGGGGATGAGTTCACAGAGGTGGGTCAATGAGTGGGTATATGTCTTAG TGAGAGAGAGGGAGAGTAGGGGATGAGTTCACGGAGGTGGGTCAATGAGTGGGTATATGTCTTAG T C ME1 Ensembl:ENSG00000065833 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:83391650..83391761 26863196 MeRIP-seq:(Medium) rs1198319589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91621,RMVar_hsa_circ_239910,RMVar_hsa_circ_369203,RMVar_hsa_circ_118786,RMVar_hsa_circ_239914,RMVar_hsa_circ_341049,RMVar_hsa_circ_239916,RMVar_hsa_circ_239918,RMVar_hsa_circ_289967,RMVar_hsa_circ_239919 108340 RMVar_ID_108340 Human_SNP_ID_284992344 m1A Human chr6 - 83430908 83430908 83430908 CCCCCGTCGCCGCCACACCCATCAGCGCGGCTACCTGCTGACACGGAACCCTCACCTCAACAAGG CCCCCGTCGCCGCCACACCCATCAGCGCGGCTGCCTGCTGACACGGAACCCTCACCTCAACAAGG T C ME1 Ensembl:ENSG00000065833 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:83407885..83431117 26863196 MeRIP-seq:(Medium) rs773779919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17421826 Human_Splice_Rec_791159 Human_miRNA_ID_2220711,Human_miRNA_ID_2483757,Human_miRNA_ID_3072132 RMVar_hsa_circ_126836,RMVar_hsa_circ_239922 108341 RMVar_ID_108341 Human_SNP_ID_284992402 m1A Human chr6 - 83430981 83430981 83430981 CCTGCACCGCGCGTGCGGCCCGCCCCGGCCTGACCCCGCCGCCGAACCCGGCGCCAGCCATGGAG CCTGCACCGCGCGTGCGGCCCGCCCCGGCCTGTCCCCGCCGCCGAACCCGGCGCCAGCCATGGAG T A ME1 Ensembl:ENSG00000065833 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:83430884..83431036 26863196 MeRIP-seq:(Medium) rs1321029322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17421826,Human_RBP_ID_26828651 Human_miRNA_ID_2146281,Human_miRNA_ID_2987710,Human_miRNA_ID_3021403 RMVar_hsa_circ_126836,RMVar_hsa_circ_239922 108342 RMVar_ID_108342 Human_SNP_ID_284992416 m1A Human chr6 + 83431000 83431000 83431000 TTCGGCGGCGGGGTCAGGCCGGGGCGGGCCGCACGCGCGGTGCAGGCGGCGGATGCTGCTGGGGT TTCGGCGGCGGGGTCAGGCCGGGGCGGGCCGCGCGCGCGGTGCAGGCGGCGGATGCTGCTGGGGT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr6:83407897..83431118;chr6:83430937..83431066 26863410 MeRIP-seq:(Medium) rs1375621038 Functional Loss SNV dbSNP153 33..33 33 - - - 108343 RMVar_ID_108343 Human_SNP_ID_285097810 m1A Human chr6 + 83859749 83859749 83859749 CGGAGCTGGAGGTGCTGTCCCGTCTGGCGGCGATCCCCGGGCAGGGCCCGGGGCCGGGGTTTGAA CGGAGCTGGAGGTGCTGTCCCGTCTGGCGGCGGTCCCCGGGCAGGGCCCGGGGCCGGGGTTTGAA A G CYB5R4 Ensembl:ENSG00000065615 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:83859705..83859792 26863196 MeRIP-seq:(Medium) rs750891052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_669355,Human_RBP_ID_4903432,Human_RBP_ID_18425689 108344 RMVar_ID_108344 Human_SNP_ID_285318538 m1A Human chr6 - 84764354 84764354 84764354 TTGGCCGGCGCGTCGCCGGTTCCTGGATCCCAACACAAGCGAGAAAGCGGAAACGCCAAATCTGT TTGGCCGGCGCGTCGCCGGTTCCTGGATCCCAGCACAAGCGAGAAAGCGGAAACGCCAAATCTGT T C TBX18 Ensembl:ENSG00000112837 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:84764297..84764428 26863196 MeRIP-seq:(Medium) rs956387444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18082359,Human_RBP_ID_18870510,Human_RBP_ID_24174455 108345 RMVar_ID_108345 Human_SNP_ID_285489845 m1A Human chr6 + 85450127 85450127 85450127 TCGCCCGGCTCGCCCGCTTTCGCACCCAGTTCACGCGCCACAGCTATGTGTCCCCGAGCCGCGCG TCGCCCGGCTCGCCCGCTTTCGCACCCAGTTCTCGCGCCACAGCTATGTGTCCCCGAGCCGCGCG A T NT5E Ensembl:ENSG00000135318 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:85450076..85450229 26863196 MeRIP-seq:(Medium) rs1371671630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4905017 108346 RMVar_ID_108346 Human_SNP_ID_285493139 m1A Human chr6 + 85464788 85464788 85464788 AGCACACTAAGGCAGCAACAATAGGTGGATGGAAACTGGAGCATTTAGGTAAGGGAGAGGGATGC AGCACACTAAGGCAGCAACAATAGGTGGATGGGAACTGGAGCATTTAGGTAAGGGAGAGGGATGC A G NT5E Ensembl:ENSG00000135318 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:85464785..85464984 26863196 MeRIP-seq:(Medium) rs557291176 Functional Loss SNV dbSNP153 33..33 33 - - - 108347 RMVar_ID_108347 Human_SNP_ID_285493145 m1A Human chr6 + 85464795 85464795 85464795 TAAGGCAGCAACAATAGGTGGATGGAAACTGGAGCATTTAGGTAAGGGAGAGGGATGCCAGAGGA TAAGGCAGCAACAATAGGTGGATGGAAACTGGCGCATTTAGGTAAGGGAGAGGGATGCCAGAGGA A C NT5E Ensembl:ENSG00000135318 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:85464785..85464893 26863196 MeRIP-seq:(Medium) rs372156734 Functional Loss SNV dbSNP153 33..33 33 - - - 108348 RMVar_ID_108348 Human_SNP_ID_285523966 m1A Human chr6 - 85593789 85593789 85593789 GTGCGCCGCCAAGTCGGTGGGGCGGGGACGCGAGGTGTGGATGGGGGGTCGCCTTGACCTCTGCC GTGCGCCGCCAAGTCGGTGGGGCGGGGACGCGTGGTGTGGATGGGGGGTCGCCTTGACCTCTGCC T A SNX14,AL589666.1 Ensembl:ENSG00000135317,Ensembl:ENSG00000271793 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:85593740..85594156 26863196 MeRIP-seq:(Medium) rs112199582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790307,Human_RBP_ID_842033,Human_RBP_ID_4899880,Human_RBP_ID_8905431,Human_RBP_ID_22462152 RMVar_hsa_circ_83693,RMVar_hsa_circ_240027 108349 RMVar_ID_108349 Human_SNP_ID_285529802 m1A Human chr6 + 85615041 85615041 85615041 CCTCTCGCACCTCGAACGCCTCTTGCTGATCCAGGACCTCCTCTCTGTGAATAACCGGCTCTACC CCTCTCGCACCTCGAACGCCTCTTGCTGATCCGGGACCTCCTCTCTGTGAATAACCGGCTCTACC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:85614912..85615185 26863196 MeRIP-seq:(Medium) rs1375959711 Functional Loss SNV dbSNP153 33..33 33 - - - 108350 RMVar_ID_108350 Human_SNP_ID_285529809 m1A Human chr6 - 85615054 85615054 85615054 TGCTCCTCCCCGCGGTAGAGCCGGTTATTCACAGAGAGGAGGTCCTGGATCAGCAAGAGGCGTTC TGCTCCTCCCCGCGGTAGAGCCGGTTATTCACTGAGAGGAGGTCCTGGATCAGCAAGAGGCGTTC T A SYNCRIP,AL589666.1 Ensembl:ENSG00000135316,Ensembl:ENSG00000271793 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:85614866..85615166 26863196 MeRIP-seq:(Medium) rs1314818884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81724,Human_RBP_ID_669611,Human_RBP_ID_1048972,Human_RBP_ID_2028620,Human_RBP_ID_3022590,Human_RBP_ID_3817631,Human_RBP_ID_4900056,Human_RBP_ID_7639251,Human_RBP_ID_8904092,Human_RBP_ID_9199332,Human_RBP_ID_15896785,Human_RBP_ID_17308303,Human_RBP_ID_18082502,Human_RBP_ID_23069704,Human_RBP_ID_26354183,Human_RBP_ID_27101511,Human_RBP_ID_27842672 Human_Splice_Rec_792845,Human_Splice_Rec_792877,Human_Splice_Rec_792899 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063 108351 RMVar_ID_108351 Human_SNP_ID_285536603 m1A Human chr6 - 85637330 85637330 85637330 TTCAAGGCACTCTTGGAAAGAACAGGCTACACACTTGATGTGACCACTGGACAGAGGAAGTATGG TTCAAGGCACTCTTGGAAAGAACAGGCTACACGCTTGATGTGACCACTGGACAGAGGAAGTATGG T C SYNCRIP Ensembl:ENSG00000135316 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:85637081..85640294 32194978 MeRIP-seq:(Medium) rs1369328362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951119,Human_RBP_ID_1048982,Human_RBP_ID_1677078,Human_RBP_ID_2028717,Human_RBP_ID_3817682,Human_RBP_ID_7639530,Human_RBP_ID_8650692,Human_RBP_ID_8904117,Human_RBP_ID_15897798,Human_RBP_ID_18870673,Human_RBP_ID_19131593,Human_RBP_ID_22462848,Human_RBP_ID_23066106,Human_RBP_ID_24174724,Human_RBP_ID_26050116 Human_Splice_Rec_792864,Human_Splice_Rec_792865,Human_Splice_Rec_792886,Human_Splice_Rec_792887,Human_Splice_Rec_792908,Human_Splice_Rec_792909,Human_Splice_Rec_792928,Human_Splice_Rec_792929 RMVar_hsa_circ_240063,RMVar_hsa_circ_284713,RMVar_hsa_circ_359214,RMVar_hsa_circ_18645,RMVar_hsa_circ_240067,RMVar_hsa_circ_304731,RMVar_hsa_circ_83165,RMVar_hsa_circ_343764,RMVar_hsa_circ_346751,RMVar_hsa_circ_347493,RMVar_hsa_circ_102309,RMVar_hsa_circ_240068,RMVar_hsa_circ_240069 108352 RMVar_ID_108352 Human_SNP_ID_285538527 m1A Human chr6 - 85642873 85642873 85642873 GCCATTTTACAACAGCTCCACTCGCGCCGGACACAGGGAGCAGCGAGCACGCGTTTCCCGCAACC GCCATTTTACAACAGCTCCACTCGCGCCGGACGCAGGGAGCAGCGAGCACGCGTTTCCCGCAACC T C SYNCRIP Ensembl:ENSG00000135316 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:85642801..85642900 26863196 MeRIP-seq:(Medium) rs891784161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80314,Human_RBP_ID_951126,Human_RBP_ID_1677098,Human_RBP_ID_4904162,Human_RBP_ID_5152382,Human_RBP_ID_5428764,Human_RBP_ID_7639594,Human_RBP_ID_8216140,Human_RBP_ID_8650706,Human_RBP_ID_8904126,Human_RBP_ID_9437866,Human_RBP_ID_15898023,Human_RBP_ID_19129583,Human_RBP_ID_22105277,Human_RBP_ID_22315015,Human_RBP_ID_22462153,Human_RBP_ID_22616891,Human_RBP_ID_23067869,Human_RBP_ID_26538560,Human_RBP_ID_27101546,Human_RBP_ID_27349489 Human_Splice_Rec_792859,Human_Splice_Rec_792879,Human_Splice_Rec_792901 RMVar_hsa_circ_240063,RMVar_hsa_circ_33404,RMVar_hsa_circ_359214,RMVar_hsa_circ_18645,RMVar_hsa_circ_304731,RMVar_hsa_circ_102309,RMVar_hsa_circ_240069 108353 RMVar_ID_108353 Human_SNP_ID_285538530 m1A Human chr6 - 85642875 85642875 85642875 CCGCCATTTTACAACAGCTCCACTCGCGCCGGACACAGGGAGCAGCGAGCACGCGTTTCCCGCAA CCGCCATTTTACAACAGCTCCACTCGCGCCGGGCACAGGGAGCAGCGAGCACGCGTTTCCCGCAA T C SYNCRIP Ensembl:ENSG00000135316 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:85642826..85642930 32194978 MeRIP-seq:(Medium) rs1262882529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80314,Human_RBP_ID_951126,Human_RBP_ID_1677098,Human_RBP_ID_4900119,Human_RBP_ID_5152382,Human_RBP_ID_5428764,Human_RBP_ID_7639594,Human_RBP_ID_8216140,Human_RBP_ID_8650706,Human_RBP_ID_8904126,Human_RBP_ID_9437866,Human_RBP_ID_15898023,Human_RBP_ID_19129583,Human_RBP_ID_22105277,Human_RBP_ID_22315015,Human_RBP_ID_22462153,Human_RBP_ID_22616892,Human_RBP_ID_23067869,Human_RBP_ID_27101546,Human_RBP_ID_27349489 Human_Splice_Rec_792859,Human_Splice_Rec_792879,Human_Splice_Rec_792901 RMVar_hsa_circ_240063,RMVar_hsa_circ_33404,RMVar_hsa_circ_359214,RMVar_hsa_circ_18645,RMVar_hsa_circ_304731,RMVar_hsa_circ_102309,RMVar_hsa_circ_240069 108354 RMVar_ID_108354 Human_SNP_ID_285538748 m1A Human chr6 - 85643267 85643265 85643267 CGACTCGGCAGGGACTGGGGGACCGGGCCGAGAGTGCGAGCGAGCGAGGGAGGGAGTGAGGGAGC CGACTCGGCAGGGACTGGGGGACCGGGCCGAG__TGCGAGCGAGCGAGGGAGGGAGTGAGGGAGC ACT A SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:85642798..85643792;chr6:85643010..85643325;chr6:85641376..85643792;chr6:85642826..85643792 26863196 MeRIP-seq:(Medium) rs1184881246 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_790299,Human_RBP_ID_841370,Human_RBP_ID_3822250,Human_RBP_ID_4900132,Human_RBP_ID_5152384,Human_RBP_ID_7639604,Human_RBP_ID_8215329,Human_RBP_ID_8944030,Human_RBP_ID_9437522,Human_RBP_ID_18425463,Human_RBP_ID_18958534,Human_RBP_ID_23294977,Human_RBP_ID_24174749,Human_RBP_ID_24554660 RMVar_hsa_circ_102309,RMVar_hsa_circ_240069 108355 RMVar_ID_108355 Human_SNP_ID_285538750 m1A Human chr6 - 85643267 85643267 85643267 CGACTCGGCAGGGACTGGGGGACCGGGCCGAGAGTGCGAGCGAGCGAGGGAGGGAGTGAGGGAGC CGACTCGGCAGGGACTGGGGGACCGGGCCGAGGGTGCGAGCGAGCGAGGGAGGGAGTGAGGGAGC T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:85642798..85643792;chr6:85643010..85643325;chr6:85641376..85643792;chr6:85642826..85643792 26863196 MeRIP-seq:(Medium) rs540049899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790299,Human_RBP_ID_841370,Human_RBP_ID_3822250,Human_RBP_ID_4900132,Human_RBP_ID_5152384,Human_RBP_ID_7639604,Human_RBP_ID_8215329,Human_RBP_ID_8944030,Human_RBP_ID_9437522,Human_RBP_ID_18425463,Human_RBP_ID_18958534,Human_RBP_ID_23294977,Human_RBP_ID_24174749,Human_RBP_ID_24554660 RMVar_hsa_circ_102309,RMVar_hsa_circ_240069 108356 RMVar_ID_108356 Human_SNP_ID_285548036 m1A Human chr6 - 85678032 85678032 85678032 TGCATCGTTTGAAATTTACTTTTTTTTGTTAGATACACGAAAAAACTTCCAGAACATCTGGGAGA TGCATCGTTTGAAATTTACTTTTTTTTGTTAGGTACACGAAAAAACTTCCAGAACATCTGGGAGA T C SNHG5 Ensembl:ENSG00000203875 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:85677870..85678225 26863410 MeRIP-seq:(Medium) rs924239522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_669663,Human_RBP_ID_1678707,Human_RBP_ID_2028778,Human_RBP_ID_5090397,Human_RBP_ID_5218906,Human_RBP_ID_5619475,Human_RBP_ID_5656709,Human_RBP_ID_7639764,Human_RBP_ID_17309101,Human_RBP_ID_17664176,Human_RBP_ID_23066162,Human_RBP_ID_26050145,Human_RBP_ID_27349503 Human_Splice_Rec_792932,Human_Splice_Rec_792933,Human_Splice_Rec_792942,Human_Splice_Rec_792943,Human_Splice_Rec_792962,Human_Splice_Rec_792963,Human_Splice_Rec_792978,Human_Splice_Rec_792979,Human_Splice_Rec_792988,Human_Splice_Rec_792989,Human_Splice_Rec_793000,Human_Splice_Rec_793001,Human_Splice_Rec_793008,Human_Splice_Rec_793009,Human_Splice_Rec_793020,Human_Splice_Rec_793021,Human_Splice_Rec_793034,Human_Splice_Rec_793035,Human_Splice_Rec_793048,Human_Splice_Rec_793049,Human_Splice_Rec_793068,Human_Splice_Rec_793069,Human_Splice_Rec_793080,Human_Splice_Rec_793081,Human_Splice_Rec_793092,Human_Splice_Rec_793093,Human_Splice_Rec_793108,Human_Splice_Rec_793109,Human_Splice_Rec_793130,Human_Splice_Rec_793131,Human_Splice_Rec_793142,Human_Splice_Rec_793143,Human_Splice_Rec_793156,Human_Splice_Rec_793157,Human_Splice_Rec_793164,Human_Splice_Rec_793165,Human_Splice_Rec_793170,Human_Splice_Rec_793171,Human_Splice_Rec_793184,Human_Splice_Rec_793185,Human_Splice_Rec_793188,Human_Splice_Rec_793189,Human_Splice_Rec_793206,Human_Splice_Rec_793207,Human_Splice_Rec_793216,Human_Splice_Rec_793217,Human_Splice_Rec_793234,Human_Splice_Rec_793238,Human_Splice_Rec_793239,Human_Splice_Rec_793248,Human_Splice_Rec_793249,Human_Splice_Rec_793254,Human_Splice_Rec_793255,Human_Splice_Rec_793262,Human_Splice_Rec_793263,Human_Splice_Rec_793270,Human_Splice_Rec_793271,Human_Splice_Rec_793280,Human_Splice_Rec_793281,Human_Splice_Rec_793290,Human_Splice_Rec_793308,Human_Splice_Rec_793309,Human_Splice_Rec_793314,Human_Splice_Rec_793320,Human_Splice_Rec_793336,Human_Splice_Rec_793342,Human_Splice_Rec_793343,Human_Splice_Rec_793352,Human_Splice_Rec_793357,Human_Splice_Rec_793364,Human_Splice_Rec_793365,Human_Splice_Rec_793368,Human_Splice_Rec_793369,Human_Splice_Rec_793378,Human_Splice_Rec_793379,Human_Splice_Rec_793383,Human_Splice_Rec_793388,Human_Splice_Rec_793389,Human_Splice_Rec_793395,Human_Splice_Rec_793402,Human_Splice_Rec_793403,Human_Splice_Rec_793405,Human_Splice_Rec_793410,Human_Splice_Rec_793416,Human_Splice_Rec_793417,Human_Splice_Rec_793424,Human_Splice_Rec_793425,Human_Splice_Rec_793430,Human_Splice_Rec_793431,Human_Splice_Rec_793437,Human_Splice_Rec_793448,Human_Splice_Rec_793449,Human_Splice_Rec_793462,Human_Splice_Rec_793463,Human_Splice_Rec_793472,Human_Splice_Rec_793478,Human_Splice_Rec_793479,Human_Splice_Rec_793486,Human_Splice_Rec_793487,Human_Splice_Rec_793494,Human_Splice_Rec_793495,Human_Splice_Rec_793506,Human_Splice_Rec_793507,Human_Splice_Rec_793512,Human_Splice_Rec_793513,Human_Splice_Rec_793520,Human_Splice_Rec_793521,Human_Splice_Rec_793536,Human_Splice_Rec_793537,Human_Splice_Rec_793546,Human_Splice_Rec_793554,Human_Splice_Rec_793555 RMVar_hsa_circ_368535,RMVar_hsa_circ_325631,RMVar_hsa_circ_333344,RMVar_hsa_circ_360969 108357 RMVar_ID_108357 Human_SNP_ID_285548082 m1A Human chr6 + 85678172 85678172 85678172 GCATCTTCAGAGCTGCTCCACTGTGCCACTGAAGACAGCGCCATTGTTCCTGCGGGAAATCGGTA GCATCTTCAGAGCTGCTCCACTGTGCCACTGAGGACAGCGCCATTGTTCCTGCGGGAAATCGGTA A G lnc-NT5E-3-002 RNACentral:URS00008B6725 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:85678126..85678200 26863196 MeRIP-seq:(Medium) rs1562133516 Functional Loss SNV dbSNP153 33..33 33 - - - 108358 RMVar_ID_108358 Human_SNP_ID_285548244 m1A Human chr6 + 85678681 85678681 85678681 CGCCACCATCTTTTGCTCGGATACTAGCCCGCAATACCCACTCACCTACCACCCGCCCAGACGCT CGCCACCATCTTTTGCTCGGATACTAGCCCGCTATACCCACTCACCTACCACCCGCCCAGACGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:85678376..85678736;chr6:85678401..85678725 26863196 MeRIP-seq:(Medium) rs535088556 Functional Loss SNV dbSNP153 33..33 33 - - - 108359 RMVar_ID_108359 Human_SNP_ID_285985788 m1A Human chr6 + 87059779 87059779 87059779 GGGGGAGGGGGAGGCGGGGGGAGGGGGAGGGGAGGCGGGGGAGGTGGGGGAGGCAGGGAGGAGGC GGGGGAGGGGGAGGCGGGGGGAGGGGGAGGGGCGGCGGGGGAGGTGGGGGAGGCAGGGAGGAGGC A C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:87059655..87059782 26863196 MeRIP-seq:(Medium) rs1479931563 Functional Loss SNV dbSNP153 33..33 33 - - - 108360 RMVar_ID_108360 Human_SNP_ID_285985789 m1A Human chr6 + 87059779 87059779 87059779 GGGGGAGGGGGAGGCGGGGGGAGGGGGAGGGGAGGCGGGGGAGGTGGGGGAGGCAGGGAGGAGGC GGGGGAGGGGGAGGCGGGGGGAGGGGGAGGGGGGGCGGGGGAGGTGGGGGAGGCAGGGAGGAGGC A G RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:87059655..87059782 26863196 MeRIP-seq:(Medium) rs1479931563 Functional Loss SNV dbSNP153 33..33 33 - - - 108361 RMVar_ID_108361 Human_SNP_ID_285992048 m1A Human chr6 - 87085830 87085830 87085830 TAATATGTTTTTTTTTCCTTCCCCTTTAGGTCACAGTAATGGGGGGTTTCAAAGTGGAGAACCAC TAATATGTTTTTTTTTCCTTCCCCTTTAGGTCCCAGTAATGGGGGGTTTCAAAGTGGAGAACCAC T G CGA Ensembl:ENSG00000135346 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:87085768..87085869 26863196 MeRIP-seq:(Medium) rs1450358294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80372 Human_Splice_Rec_793584,Human_Splice_Rec_793592,Human_Splice_Rec_793598 RMVar_hsa_circ_108692,RMVar_hsa_circ_240087,RMVar_hsa_circ_95850,RMVar_hsa_circ_240086 108362 RMVar_ID_108362 Human_SNP_ID_286011026 m1A Human chr6 + 87155636 87155636 87155636 GAGGCCGAGCAGGAGAGGTTGAGTTGCGGCGAAGGCGGCTGCGTCGCGGAGCTGCAGCGCCTGGG GAGGCCGAGCAGGAGAGGTTGAGTTGCGGCGACGGCGGCTGCGTCGCGGAGCTGCAGCGCCTGGG A C ZNF292 Ensembl:ENSG00000188994 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:87155596..87155707;chr6:87155590..87155756;chr6:87155587..87155734;chr6:87155586..87155732 26863196 MeRIP-seq:(Medium) rs1228282485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4900212,Human_RBP_ID_8237439,Human_RBP_ID_9400889,Human_RBP_ID_18425466,Human_RBP_ID_19017272,Human_RBP_ID_22418790,Human_RBP_ID_22460786,Human_RBP_ID_23214904,Human_RBP_ID_26354188,Human_RBP_ID_27827847 Human_Splice_Rec_793614 108363 RMVar_ID_108363 Human_SNP_ID_286023539 m1A Human chr6 - 87203655 87203655 87203655 TGGGGTCTGATGCCTTCCCCCAACATGATGCTACTACTCAATCTGGGCTTTGACATTCCACTCTG TGGGGTCTGATGCCTTCCCCCAACATGATGCTCCTACTCAATCTGGGCTTTGACATTCCACTCTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:87203653..87203918 26863196 MeRIP-seq:(Medium) rs1341447640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240088 108364 RMVar_ID_108364 Human_SNP_ID_286053632 m1A Human chr6 + 87322629 87322629 87322629 CGTCTCGGGCGAGGAGAGGAGGTGACCCCGCGAAAGGTAAGCGGCGGCTTCGGTGGTGTTGAGTG CGTCTCGGGCGAGGAGAGGAGGTGACCCCGCGGAAGGTAAGCGGCGGCTTCGGTGGTGTTGAGTG A G SMIM8 Ensembl:ENSG00000111850 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:87322617..87322690;chr6:87322603..87322688 26863196 MeRIP-seq:(Medium) rs1430172306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19131607 Human_Splice_Rec_793695,Human_Splice_Rec_793701,Human_Splice_Rec_793707,Human_Splice_Rec_793711,Human_Splice_Rec_793723,Human_Splice_Rec_793727 108365 RMVar_ID_108365 Human_SNP_ID_286053633 m1A Human chr6 + 87322629 87322629 87322629 CGTCTCGGGCGAGGAGAGGAGGTGACCCCGCGAAAGGTAAGCGGCGGCTTCGGTGGTGTTGAGTG CGTCTCGGGCGAGGAGAGGAGGTGACCCCGCGTAAGGTAAGCGGCGGCTTCGGTGGTGTTGAGTG A T SMIM8 Ensembl:ENSG00000111850 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:87322617..87322690;chr6:87322603..87322688 26863196 MeRIP-seq:(Medium) rs1430172306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19131607 Human_Splice_Rec_793695,Human_Splice_Rec_793701,Human_Splice_Rec_793707,Human_Splice_Rec_793711,Human_Splice_Rec_793723,Human_Splice_Rec_793727 108366 RMVar_ID_108366 Human_SNP_ID_286053634 m1A Human chr6 + 87322631 87322631 87322631 TCTCGGGCGAGGAGAGGAGGTGACCCCGCGAAAGGTAAGCGGCGGCTTCGGTGGTGTTGAGTGGC TCTCGGGCGAGGAGAGGAGGTGACCCCGCGAACGGTAAGCGGCGGCTTCGGTGGTGTTGAGTGGC A C SMIM8 Ensembl:ENSG00000111850 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:87322615..87322686 26863196 MeRIP-seq:(Medium) rs1481532242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19131607 Human_Splice_Rec_793695,Human_Splice_Rec_793701,Human_Splice_Rec_793707,Human_Splice_Rec_793711,Human_Splice_Rec_793723,Human_Splice_Rec_793727 108367 RMVar_ID_108367 Human_SNP_ID_286080993 m1A Human chr6 - 87437847 87437847 87437847 AGGCACCGTCTCTAGAAAAACTAAAACTAAAAAAAAAAAAAAAAAAAAAAAAAATTAGCCAGGCA AGGCACCGTCTCTAGAAAAACTAAAACTAAAACAAAAAAAAAAAAAAAAAAAAATTAGCCAGGCA T G RF00017-4499 RNACentral:URS000098B860 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:87437831..87437919 26863410 MeRIP-seq:(Medium) rs892956380 Functional Loss SNV dbSNP153 33..33 33 - - - 108368 RMVar_ID_108368 Human_SNP_ID_286145937 m1A Human chr6 - 87701716 87701716 87701716 ACCCTCTTCTTTCGTCACCCGTCCCCGACCCCACCCGAGCCCGGCGCCTCAGCTGCCCCCGGCCA ACCCTCTTCTTTCGTCACCCGTCCCCGACCCCCCCCGAGCCCGGCGCCTCAGCTGCCCCCGGCCA T G AKIRIN2 Ensembl:ENSG00000135334 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:87701615..87701871 26863196 MeRIP-seq:(Medium) rs1338432787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251554,Human_RBP_ID_790314,Human_RBP_ID_5134173,Human_RBP_ID_9336238,Human_RBP_ID_17091282,Human_RBP_ID_17421832,Human_RBP_ID_18958536,Human_RBP_ID_22105301,Human_RBP_ID_22315221,Human_RBP_ID_27101798 RMVar_hsa_circ_87553,RMVar_hsa_circ_240156 108369 RMVar_ID_108369 Human_SNP_ID_286480697 m1A Human chr6 - 89080801 89080801 89080801 AAGATAGGGTGGCGGCGATGGATGCTGCTAGGAGAGCCTGAGAAGATCGCGGAACATGACTCGGG AAGATAGGGTGGCGGCGATGGATGCTGCTAGGCGAGCCTGAGAAGATCGCGGAACATGACTCGGG T G lnc-SRSF12-2 RNACentral:URS0000D59E0F lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89080751..89081273 26863196 MeRIP-seq:(Medium) rs1487598583 Functional Loss SNV dbSNP153 33..33 33 - - - 108370 RMVar_ID_108370 Human_SNP_ID_286480781 m1A Human chr6 - 89080947 89080947 89080947 AGTAACCTCGGGAGGAAAAGCCAAGCGGCGCAAGGCGGCCACCCAGGACGAGCGGCTCCCGCTGC AGTAACCTCGGGAGGAAAAGCCAAGCGGCGCAGGGCGGCCACCCAGGACGAGCGGCTCCCGCTGC T C lnc-SRSF12-2 RNACentral:URS0000D59E0F lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr6:89080751..89081182;chr6:89080751..89081150 26863196 MeRIP-seq:(Medium) rs1017268237 Functional Loss SNV dbSNP153 33..33 33 - - - 108371 RMVar_ID_108371 Human_SNP_ID_286481922 m1A Human chr6 - 89083844 89083844 89083844 GTGGCAAGTTATATTTGCTTTTCTGTCTGTTTATCTTTGGTTGCTCATACAAGTGTATACCATGA GTGGCAAGTTATATTTGCTTTTCTGTCTGTTTGTCTTTGGTTGCTCATACAAGTGTATACCATGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:89083754..89083855 26863196 MeRIP-seq:(Medium) rs146407886 Functional Loss SNV dbSNP153 33..33 33 - - - 108372 RMVar_ID_108372 Human_SNP_ID_286497496 m1A Human chr6 + 89146145 89146145 89146145 AGAGGGCGCAGAGGGCAGCGGGCTTGGGCAGCATGAGGCCCGGAGGGGAGCGGCCCGTGGAAGGG AGAGGGCGCAGAGGGCAGCGGGCTTGGGCAGCGTGAGGCCCGGAGGGGAGCGGCCCGTGGAAGGG A G PM20D2 Ensembl:ENSG00000146281 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89146062..89146557 26863196 MeRIP-seq:(Medium) rs1172989218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791040,Human_RBP_ID_4905034,Human_RBP_ID_18083165,Human_RBP_ID_23120379 RMVar_hsa_circ_240192 108373 RMVar_ID_108373 Human_SNP_ID_286501351 m1A Human chr6 - 89161510 89161510 89161510 ACTGGCCCTCTTGGCCAGCACTCCACACTGCCACCTACTCCCTTTCTTCTCTTCTGTGACACAGC ACTGGCCCTCTTGGCCAGCACTCCACACTGCCGCCTACTCCCTTTCTTCTCTTCTGTGACACAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89161462..89161583 26863196 MeRIP-seq:(Medium) rs1398303805 Functional Loss SNV dbSNP153 33..33 33 - - - 108374 RMVar_ID_108374 Human_SNP_ID_286501561 m1A Human chr6 - 89162229 89162229 89162229 ATTCTACTGCATTTACAAACTGTTCTTCTTGAAGTTTCAGTTTAAAGTCCTCTCTGATTCCTTCC ATTCTACTGCATTTACAAACTGTTCTTCTTGACGTTTCAGTTTAAAGTCCTCTCTGATTCCTTCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:89161828..89162245 32194978 MeRIP-seq:(Medium) rs764003319 Functional Loss SNV dbSNP153 33..33 33 - - - 108375 RMVar_ID_108375 Human_SNP_ID_286502276 m1A Human chr6 - 89165214 89165214 89165214 AAGAGATAACTCAGGTAAAAAGTTAGAAATGTATAAAACACCATCAGACAGGTTTTTAAAAAACA AAGAGATAACTCAGGTAAAAAGTTAGAAATGTGTAAAACACCATCAGACAGGTTTTTAAAAAACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:89165118..89165268 32194978 MeRIP-seq:(Medium) rs961278393 Functional Loss SNV dbSNP153 33..33 33 - - - 108376 RMVar_ID_108376 Human_SNP_ID_286547571 m1A Human chr6 + 89352660 89352660 89352660 CCGCTGCCCGGGTCTCAGCGCGGCTCGGGCGGACGGGGCCTGGCCGAGGAGCCTCGGCAAATGCC CCGCTGCCCGGGTCTCAGCGCGGCTCGGGCGGGCGGGGCCTGGCCGAGGAGCCTCGGCAAATGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:89352611..89352800 26863196 MeRIP-seq:(Medium) rs1343960228 Functional Loss SNV dbSNP153 33..33 33 - - - 108377 RMVar_ID_108377 Human_SNP_ID_286560693 m1A Human chr6 + 89411980 89411980 89411980 CGTCGTCCTCGTCCTGCGGCTGCGGCTTCCCCAGCACCTGGCTCATCGTGCCCACCGGCCGGCCG CGTCGTCCTCGTCCTGCGGCTGCGGCTTCCCCTGCACCTGGCTCATCGTGCCCACCGGCCGGCCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89411859..89412005 26863196 MeRIP-seq:(Medium) rs771253426 Functional Loss SNV dbSNP153 33..33 33 - - - 108378 RMVar_ID_108378 Human_SNP_ID_286618617 m1A Human chr6 - 89658877 89658877 89658877 CCTTTGGAGATAAAAGAAAAACCAGAAGAAGCAGGTCATGAAGCTGAGGAAAGAGGAGAGACCGA CCTTTGGAGATAAAAGAAAAACCAGAAGAAGCCGGTCATGAAGCTGAGGAAAGAGGAGAGACCGA T G MDN1 Ensembl:ENSG00000112159 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:89658587..89658925 26863196 MeRIP-seq:(Medium) rs1444218525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13506,Human_RBP_ID_947826,Human_RBP_ID_3024093,Human_RBP_ID_19018903,Human_RBP_ID_24548445,Human_RBP_ID_24554663,Human_RBP_ID_27828775 Human_Splice_Rec_795092,Human_Splice_Rec_795294 Human_miRNA_ID_2998188 RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_104524,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_240237,RMVar_hsa_circ_94012,RMVar_hsa_circ_240238,RMVar_hsa_circ_240240,RMVar_hsa_circ_84458,RMVar_hsa_circ_240239 108379 RMVar_ID_108379 Human_SNP_ID_286619164 m1A Human chr6 - 89661393 89661393 89661393 TCTTTCAGAAACAAAGAGACCGGTTAGAACTCACATTAGTGAACAGTAATTGATTTCTCTTTTGA TCTTTCAGAAACAAAGAGACCGGTTAGAACTCCCATTAGTGAACAGTAATTGATTTCTCTTTTGA T G MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89661391..89661607 26863196 MeRIP-seq:(Medium) rs761513521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15908479 RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_104524,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_240237,RMVar_hsa_circ_94012,RMVar_hsa_circ_240238,RMVar_hsa_circ_240240,RMVar_hsa_circ_84458,RMVar_hsa_circ_240239 108380 RMVar_ID_108380 Human_SNP_ID_286619547 m1A Human chr6 - 89662793 89662793 89662793 TAAAACTGAAGAAACAGGACCAGGAATGGATGAGGTAATTCAAAGATTTCTCCCCTCCCAAACAA TAAAACTGAAGAAACAGGACCAGGAATGGATGCGGTAATTCAAAGATTTCTCCCCTCCCAAACAA T G MDN1 Ensembl:ENSG00000112159 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:89662791..89662975 26863196 MeRIP-seq:(Medium) rs772571710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15908487,Human_RBP_ID_23067609,Human_RBP_ID_23120292,Human_RBP_ID_26354229 Human_Splice_Rec_795087,Human_Splice_Rec_795289 RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_71283,RMVar_hsa_circ_94012,RMVar_hsa_circ_240238,RMVar_hsa_circ_240240,RMVar_hsa_circ_84458,RMVar_hsa_circ_240239,RMVar_hsa_circ_265859,RMVar_hsa_circ_53766,RMVar_hsa_circ_269533 108381 RMVar_ID_108381 Human_SNP_ID_286619557 m1A Human chr6 + 89662843 89662831 89662843 GTTTCTTCAGTTTTATTGTCTTCTTCCTCCTCATCTTCCTCCTCATCATCATCACCCCAAAGCCT GTTTCTTCAGTTTTATTGTCT____________TCTTCCTCCTCATCATCATCACCCCAAAGCCT TTCTTCCTCCTCA T LOC101929057 RNACentral:URS000075A3AB lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:89658201..89668100 26863196 MeRIP-seq:(Medium) rs376185382 Functional Loss DEL dbSNP153 22..33 33 - - - 108382 RMVar_ID_108382 Human_SNP_ID_286619562 m1A Human chr6 - 89662841 89662841 89662841 GCTTTGGGGTGATGATGATGAGGAGGAAGATGAGGAGGAAGAAGACAATAAAACTGAAGAAACAG GCTTTGGGGTGATGATGATGAGGAGGAAGATGTGGAGGAAGAAGACAATAAAACTGAAGAAACAG T A MDN1 Ensembl:ENSG00000112159 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89662760..89663005 26863196 MeRIP-seq:(Medium) rs1286255632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13508,Human_RBP_ID_79537,Human_RBP_ID_215488,Human_RBP_ID_947828,Human_RBP_ID_4901329,Human_RBP_ID_7645109,Human_RBP_ID_8237236,Human_RBP_ID_9199815,Human_RBP_ID_23067609,Human_RBP_ID_23120292,Human_RBP_ID_26050482,Human_RBP_ID_26354230 Human_Splice_Rec_795087,Human_Splice_Rec_795289 RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_71283,RMVar_hsa_circ_94012,RMVar_hsa_circ_240238,RMVar_hsa_circ_240240,RMVar_hsa_circ_84458,RMVar_hsa_circ_240239,RMVar_hsa_circ_265859,RMVar_hsa_circ_53766,RMVar_hsa_circ_269533 108383 RMVar_ID_108383 Human_SNP_ID_286619957 m1A Human chr6 + 89664439 89664439 89664439 CCTTATTAGGAACATGTAATTTCCTGGATAAAATATTTATGCTTTCAAAAACAAGAATGAAGTGA CCTTATTAGGAACATGTAATTTCCTGGATAAACTATTTATGCTTTCAAAAACAAGAATGAAGTGA A C LOC101929057 RNACentral:URS000075A3AB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89664437..89664575 26863196 MeRIP-seq:(Medium) rs1562053270 Functional Loss SNV dbSNP153 33..33 33 - - - 108384 RMVar_ID_108384 Human_SNP_ID_286624127 m1A Human chr6 - 89680637 89680637 89680637 AACGCATGAGGAAGATGTGCCTGACGTTCATGAAGGAGAGCCCCCTGCCTCGCCTTGTGGAGGGC AACGCATGAGGAAGATGTGCCTGACGTTCATGCAGGAGAGCCCCCTGCCTCGCCTTGTGGAGGGC T G MDN1 Ensembl:ENSG00000112159 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:89680612..89680696 26863410 MeRIP-seq:(Medium) rs779312574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4901390,Human_RBP_ID_18871328 Human_Splice_Rec_795063,Human_Splice_Rec_795265 RMVar_hsa_circ_14738,RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_27598,RMVar_hsa_circ_94012,RMVar_hsa_circ_240238,RMVar_hsa_circ_240240,RMVar_hsa_circ_84458,RMVar_hsa_circ_240239,RMVar_hsa_circ_53766,RMVar_hsa_circ_352792,RMVar_hsa_circ_269533,RMVar_hsa_circ_95989,RMVar_hsa_circ_116496,RMVar_hsa_circ_240241,RMVar_hsa_circ_125853,RMVar_hsa_circ_240243,RMVar_hsa_circ_6007,RMVar_hsa_circ_240242,RMVar_hsa_circ_26042,RMVar_hsa_circ_240245,RMVar_hsa_circ_42257,RMVar_hsa_circ_240244,RMVar_hsa_circ_67583,RMVar_hsa_circ_107596,RMVar_hsa_circ_265479,RMVar_hsa_circ_104813,RMVar_hsa_circ_240246,RMVar_hsa_circ_275734,RMVar_hsa_circ_346002,RMVar_hsa_circ_359123,RMVar_hsa_circ_283260,RMVar_hsa_circ_61890,RMVar_hsa_circ_21321,RMVar_hsa_circ_128122,RMVar_hsa_circ_240248,RMVar_hsa_circ_240249,RMVar_hsa_circ_337215,RMVar_hsa_circ_15055,RMVar_hsa_circ_240250 108385 RMVar_ID_108385 Human_SNP_ID_286634586 m1A Human chr6 + 89721526 89721526 89721526 CCCTGTGTGGAGCAAGTTTTAAAGAAGCAAAGAACTCAGAATTCATGCTTGAAGAAATGCAGGCA CCCTGTGTGGAGCAAGTTTTAAAGAAGCAAAGGACTCAGAATTCATGCTTGAAGAAATGCAGGCA A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878986217 Functional Loss SNV dbSNP153 33..33 33 - - - 108386 RMVar_ID_108386 Human_SNP_ID_286658346 m1A Human chr6 - 89810612 89810612 89810612 TATTGGAGTGATAAATCTGTGAGACAAGGAACAGCAGGGATTGATGATGACAACCAGAAGCTAGG TATTGGAGTGATAAATCTGTGAGACAAGGAACGGCAGGGATTGATGATGACAACCAGAAGCTAGG T C MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89810611..89810681 26863196 MeRIP-seq:(Medium) rs905043138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15910730 RMVar_hsa_circ_240319,RMVar_hsa_circ_86713 108387 RMVar_ID_108387 Human_SNP_ID_286660850 m1A Human chr6 + 89819692 89819692 89819692 GCGTCCCCAAGCCGCCGAGGTCCCAGTGCCCGAGCAGCCAGCAACTACGCCCGCAGGAAAGGCGT GCGTCCCCAAGCCGCCGAGGTCCCAGTGCCCGGGCAGCCAGCAACTACGCCCGCAGGAAAGGCGT A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89819453..89819767 26863196 MeRIP-seq:(Medium) rs1443826842 Functional Loss SNV dbSNP153 33..33 33 - - - 108388 RMVar_ID_108388 Human_SNP_ID_286660859 m1A Human chr6 - 89819724 89819724 89819724 CCCCTCTCCCGGTGTAGGCGCTGGAGCTGAGGACGCCTTTCCTGCGGGCGTAGTTGCTGGCTGCT CCCCTCTCCCGGTGTAGGCGCTGGAGCTGAGGTCGCCTTTCCTGCGGGCGTAGTTGCTGGCTGCT T A MDN1 Ensembl:ENSG00000112159 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:89819462..89819746 26863196 MeRIP-seq:(Medium) rs1304387019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18450829 108389 RMVar_ID_108389 Human_SNP_ID_286660860 m1A Human chr6 - 89819724 89819724 89819724 CCCCTCTCCCGGTGTAGGCGCTGGAGCTGAGGACGCCTTTCCTGCGGGCGTAGTTGCTGGCTGCT CCCCTCTCCCGGTGTAGGCGCTGGAGCTGAGGGCGCCTTTCCTGCGGGCGTAGTTGCTGGCTGCT T C MDN1 Ensembl:ENSG00000112159 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:89819462..89819746 26863196 MeRIP-seq:(Medium) rs1304387019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18450829 108390 RMVar_ID_108390 Human_SNP_ID_286660861 m1A Human chr6 - 89819727 89819727 89819727 GTGCCCCTCTCCCGGTGTAGGCGCTGGAGCTGAGGACGCCTTTCCTGCGGGCGTAGTTGCTGGCT GTGCCCCTCTCCCGGTGTAGGCGCTGGAGCTGTGGACGCCTTTCCTGCGGGCGTAGTTGCTGGCT T A MDN1 Ensembl:ENSG00000112159 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:89819574..89819755;chr6:89819527..89819746 26863196 MeRIP-seq:(Medium) rs1277538286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18450829 108391 RMVar_ID_108391 Human_SNP_ID_286663544 m1A Human chr6 + 89829947 89829947 89829947 TCTTGGGCCGGGCAGGGCGGGTAAGTTGTCGTAGGGGCCCGGTCCGTGAGGGACTGCTAAGGAAG TCTTGGGCCGGGCAGGGCGGGTAAGTTGTCGTGGGGGCCCGGTCCGTGAGGGACTGCTAAGGAAG A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:89829901..89830075 26863196 MeRIP-seq:(Medium) rs923128430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_670308,Human_RBP_ID_4901759,Human_RBP_ID_5451548,Human_RBP_ID_8904591,Human_RBP_ID_15910931,Human_RBP_ID_18083480,Human_RBP_ID_18425471,Human_RBP_ID_23067873,Human_RBP_ID_27842479 RMVar_hsa_circ_84548,RMVar_hsa_circ_240323 108392 RMVar_ID_108392 Human_SNP_ID_286663550 m1A Human chr6 - 89829957 89829957 89829957 CATGCAGCCTCTTCCTTAGCAGTCCCTCACGGACCGGGCCCCTACGACAACTTACCCGCCCTGCC CATGCAGCCTCTTCCTTAGCAGTCCCTCACGGTCCGGGCCCCTACGACAACTTACCCGCCCTGCC T A L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:89829901..89830200 26863196 MeRIP-seq:(Medium) rs939993952 Functional Loss SNV dbSNP153 33..33 33 - - - 108393 RMVar_ID_108393 Human_SNP_ID_286672120 m1A Human chr6 + 89862434 89862434 89862434 TTATCAGGTTGGCGAGGGTAGCTCAAATGAGGATAGTAGAAGAGGAAGAAAAGATATTAGACATA TTATCAGGTTGGCGAGGGTAGCTCAAATGAGGGTAGTAGAAGAGGAAGAAAAGATATTAGACATA A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:89862368..89862513 26863196 MeRIP-seq:(Medium) rs1284091401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1049210,Human_RBP_ID_2030023,Human_RBP_ID_7645868,Human_RBP_ID_8904602,Human_RBP_ID_15911840,Human_RBP_ID_23066571 RMVar_hsa_circ_98471,RMVar_hsa_circ_279621,RMVar_hsa_circ_366469,RMVar_hsa_circ_240327,RMVar_hsa_circ_240328,RMVar_hsa_circ_23292,RMVar_hsa_circ_306546,RMVar_hsa_circ_66501,RMVar_hsa_circ_266534,RMVar_hsa_circ_284148,RMVar_hsa_circ_361051,RMVar_hsa_circ_290715,RMVar_hsa_circ_271996,RMVar_hsa_circ_240333,RMVar_hsa_circ_240334,RMVar_hsa_circ_240332 108394 RMVar_ID_108394 Human_SNP_ID_621560207 m1A Human chr17 + 30116863 30116863 30116863 ACACGGGAGCAAGATGGCGATTCCGGGCAGGCAGTGAGTGATCCGGGAGTTAGGGTCAGGCTGGG ACACGGGAGCAAGATGGCGATTCCGGGCAGGCGGTGAGTGATCCGGGAGTTAGGGTCAGGCTGGG A G NSRP1 Ensembl:ENSG00000126653 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:30116826..30117068 26863196 MeRIP-seq:(Medium) rs1437731827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6577137,Human_RBP_ID_12950971,Human_RBP_ID_22948777 Human_Splice_Rec_1799877,Human_Splice_Rec_1799887,Human_Splice_Rec_1799891,Human_Splice_Rec_1799901,Human_Splice_Rec_1799913,Human_Splice_Rec_1799923,Human_Splice_Rec_1799931,Human_Splice_Rec_1799943,Human_Splice_Rec_1799949,Human_Splice_Rec_1799963,Human_Splice_Rec_1799973 108395 RMVar_ID_108395 Human_SNP_ID_621560214 m1A Human chr17 + 30116878 30116876 30116878 GGCGATTCCGGGCAGGCAGTGAGTGATCCGGGAGTTAGGGTCAGGCTGGGGGATGAGAAACTACG GGCGATTCCGGGCAGGCAGTGAGTGATCCGG__GTTAGGGTCAGGCTGGGGGATGAGAAACTACG GGA G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30116826..30117063 26863196 MeRIP-seq:(Medium) rs1298579820 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5186109,Human_RBP_ID_6577139,Human_RBP_ID_12950971,Human_RBP_ID_17888711,Human_RBP_ID_18438659,Human_RBP_ID_22062603,Human_RBP_ID_22948777 108396 RMVar_ID_108396 Human_SNP_ID_621560217 m1A Human chr17 + 30116878 30116878 30116878 GGCGATTCCGGGCAGGCAGTGAGTGATCCGGGAGTTAGGGTCAGGCTGGGGGATGAGAAACTACG GGCGATTCCGGGCAGGCAGTGAGTGATCCGGGGGTTAGGGTCAGGCTGGGGGATGAGAAACTACG A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30116826..30117063 26863196 MeRIP-seq:(Medium) rs754075805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5186109,Human_RBP_ID_6577139,Human_RBP_ID_12950971,Human_RBP_ID_17888711,Human_RBP_ID_18438659,Human_RBP_ID_22062603,Human_RBP_ID_22948777 108397 RMVar_ID_108397 Human_SNP_ID_621560218 m1A Human chr17 + 30116878 30116878 30116878 GGCGATTCCGGGCAGGCAGTGAGTGATCCGGGAGTTAGGGTCAGGCTGGGGGATGAGAAACTACG GGCGATTCCGGGCAGGCAGTGAGTGATCCGGGTGTTAGGGTCAGGCTGGGGGATGAGAAACTACG A T NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30116826..30117063 26863196 MeRIP-seq:(Medium) rs754075805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5186109,Human_RBP_ID_6577139,Human_RBP_ID_12950971,Human_RBP_ID_17888711,Human_RBP_ID_18438659,Human_RBP_ID_22062603,Human_RBP_ID_22948777 108398 RMVar_ID_108398 Human_SNP_ID_621560222 m1A Human chr17 - 30116886 30116886 30116886 ACAGTCGCCGTAGTTTCTCATCCCCCAGCCTGACCCTAACTCCCGGATCACTCACTGCCTGCCCG ACAGTCGCCGTAGTTTCTCATCCCCCAGCCTGTCCCTAACTCCCGGATCACTCACTGCCTGCCCG T A AC104984.3 Ensembl:ENSG00000265394 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30116837..30117051 26863196 MeRIP-seq:(Medium) rs1455252037 Functional Loss SNV dbSNP153 33..33 33 - - - 108399 RMVar_ID_108399 Human_SNP_ID_621577627 m1A Human chr17 + 30185528 30185527 30185528 ACAGACTCACAGAGGAAGGGCAAGAGAAGGGTAAAGAACAAGAGAGACCACCTGAGGCAGTGAGC ACAGACTCACAGAGGAAGGGCAAGAGAAGGGT_AAGAACAAGAGAGACCACCTGAGGCAGTGAGC TA T NSRP1 Ensembl:ENSG00000126653 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30185477..30185665 26863196 MeRIP-seq:(Medium) rs1261981928 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26331538 108400 RMVar_ID_108400 Human_SNP_ID_621593050 m1A Human chr17 - 30249090 30249090 30249090 AGTGGTGGTGGACAGGAAGCATGTCCCTGAAGAGGTGCTAGCTGTGTTAGAGCAGGAACCCATTA AGTGGTGGTGGACAGGAAGCATGTCCCTGAAGTGGTGCTAGCTGTGTTAGAGCAGGAACCCATTA T A BLMH Ensembl:ENSG00000108578 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:30249040..30249190 32194978 MeRIP-seq:(Medium) rs760171440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_486433,Human_RBP_ID_896384,Human_RBP_ID_1090351,Human_RBP_ID_1853382,Human_RBP_ID_12953206,Human_RBP_ID_18191208,Human_RBP_ID_22442869,Human_RBP_ID_23210290,Human_RBP_ID_23719346,Human_RBP_ID_26958382,Human_RBP_ID_27450777 Human_Splice_Rec_1800168,Human_Splice_Rec_1800188 Human_miRNA_ID_739454,Human_miRNA_ID_743470,Human_miRNA_ID_747474 108401 RMVar_ID_108401 Human_SNP_ID_621598128 m1A Human chr17 - 30272770 30272770 30272770 ACAACAACCAGCCCATTGACTTCCTGAAAAAGATGGTTGCTGCCTCCATCAAAGATGGAGAGGTT ACAACAACCAGCCCATTGACTTCCTGAAAAAGGTGGTTGCTGCCTCCATCAAAGATGGAGAGGTT T C BLMH Ensembl:ENSG00000108578 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:30272766..30272866 32194978 MeRIP-seq:(Medium) rs752080864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1853392,Human_RBP_ID_3517786,Human_RBP_ID_22444454 Human_Splice_Rec_1800161,Human_Splice_Rec_1800181,Human_Splice_Rec_1800199,Human_Splice_Rec_1800215,Human_Splice_Rec_1800219 Human_miRNA_ID_692559,Human_miRNA_ID_1302452,Human_miRNA_ID_2476398,Human_miRNA_ID_2962182 RMVar_hsa_circ_1766,RMVar_hsa_circ_272138,RMVar_hsa_circ_347299,RMVar_hsa_circ_372126,RMVar_hsa_circ_278848,RMVar_hsa_circ_72937,RMVar_hsa_circ_39152,RMVar_hsa_circ_183218,RMVar_hsa_circ_183219,RMVar_hsa_circ_183220,RMVar_hsa_circ_40099,RMVar_hsa_circ_326891,RMVar_hsa_circ_53272,RMVar_hsa_circ_267743 108402 RMVar_ID_108402 Human_SNP_ID_621602461 m1A Human chr17 - 30291507 30291507 30291507 TGCGTTAAAATCCTGTTTGGTCTCCCAACAGGACTGAATTCGGAGAAGGTAGCTGCTCTGATACA TGCGTTAAAATCCTGTTTGGTCTCCCAACAGGGCTGAATTCGGAGAAGGTAGCTGCTCTGATACA T C BLMH Ensembl:ENSG00000108578 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30291476..30291525 26863196 MeRIP-seq:(Medium) rs1447842727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899736,Human_RBP_ID_4470463,Human_RBP_ID_26812089 Human_Splice_Rec_1800148,Human_Splice_Rec_1800170,Human_Splice_Rec_1800190,Human_Splice_Rec_1800191,Human_Splice_Rec_1800222,Human_Splice_Rec_1800242,Human_Splice_Rec_1800248,Human_Splice_Rec_1800252 RMVar_hsa_circ_19860,RMVar_hsa_circ_372126,RMVar_hsa_circ_183220,RMVar_hsa_circ_267743,RMVar_hsa_circ_265667 108403 RMVar_ID_108403 Human_SNP_ID_621623545 m1A Human chr17 + 30379019 30379019 30379019 AGCGGCCGGGACGAGCGGCCGCCTTGGCGGCTAGGGCGGCTCCTGTTGCTCATGTGCCTGCTGCT AGCGGCCGGGACGAGCGGCCGCCTTGGCGGCTCGGGCGGCTCCTGTTGCTCATGTGCCTGCTGCT A C CPD Ensembl:ENSG00000108582 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:30378973..30379148 26863196 MeRIP-seq:(Medium) rs1406425215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235865,Human_RBP_ID_764734,Human_RBP_ID_821033,Human_RBP_ID_903329,Human_RBP_ID_4416702,Human_RBP_ID_18470018,Human_RBP_ID_22443554 Human_miRNA_ID_3010874 RMVar_hsa_circ_183221,RMVar_hsa_circ_108959 108404 RMVar_ID_108404 Human_SNP_ID_621628903 m1A Human chr17 + 30401444 30401444 30401444 TCCTCTTCCTCCTCTTCCTCTTCTTCTTCCTCATCTTCTTCTTCTTCTTCCTCTTCTTCTTCTTC TCCTCTTCCTCCTCTTCCTCTTCTTCTTCCTCCTCTTCTTCTTCTTCTTCCTCTTCTTCTTCTTC A C CPD Ensembl:ENSG00000108582 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30401437..30401502 26863196 MeRIP-seq:(Medium) rs1293093627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20290404 RMVar_hsa_circ_21305,RMVar_hsa_circ_57618,RMVar_hsa_circ_183221,RMVar_hsa_circ_108959,RMVar_hsa_circ_368205,RMVar_hsa_circ_70748,RMVar_hsa_circ_47955 108405 RMVar_ID_108405 Human_SNP_ID_621628904 m1A Human chr17 + 30401444 30401444 30401444 TCCTCTTCCTCCTCTTCCTCTTCTTCTTCCTCATCTTCTTCTTCTTCTTCCTCTTCTTCTTCTTC TCCTCTTCCTCCTCTTCCTCTTCTTCTTCCTCTTCTTCTTCTTCTTCTTCCTCTTCTTCTTCTTC A T CPD Ensembl:ENSG00000108582 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30401437..30401502 26863196 MeRIP-seq:(Medium) rs1293093627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20290404 RMVar_hsa_circ_21305,RMVar_hsa_circ_57618,RMVar_hsa_circ_183221,RMVar_hsa_circ_108959,RMVar_hsa_circ_368205,RMVar_hsa_circ_70748,RMVar_hsa_circ_47955 108406 RMVar_ID_108406 Human_SNP_ID_621656796 m1A Human chr17 + 30523395 30523395 30523395 TGAGGAGCGTCTCTGTCTGGCCACCCCGTCTGAGAAGTGAGGAGACCTCCGCCCGGCAGCCGCCC TGAGGAGCGTCTCTGTCTGGCCACCCCGTCTGGGAAGTGAGGAGACCTCCGCCCGGCAGCCGCCC A G GOSR1 Ensembl:ENSG00000108587 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30523344..30523419 26863196 MeRIP-seq:(Medium) rs1236329184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4417017,Human_RBP_ID_6578548,Human_RBP_ID_12954856,Human_RBP_ID_26457289 RMVar_hsa_circ_108830,RMVar_hsa_circ_183236 108407 RMVar_ID_108407 Human_SNP_ID_621675755 m1A Human chr17 - 30600955 30600955 30600955 CAAGTCAACAGGTACCCCGCGCCAGCTCGCCCACCCGGCGGCTGCCCAGCCCGGCCGCCGCTCCC CAAGTCAACAGGTACCCCGCGCCAGCTCGCCCCCCCGGCGGCTGCCCAGCCCGGCCGCCGCTCCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30600909..30601019 26863196 MeRIP-seq:(Medium) rs1567945296 Functional Loss SNV dbSNP153 33..33 33 - - - 108408 RMVar_ID_108408 Human_SNP_ID_621702319 m1A Human chr17 - 30709015 30709015 30709015 GACCGAGCCGGAGCCGGGAACCAGCAATGACAAGCCGCCAGCTCTCCCCTCTCCCCGGCGCACCC GACCGAGCCGGAGCCGGGAACCAGCAATGACAGGCCGCCAGCTCTCCCCTCTCCCCGGCGCACCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30709008..30709114 26863196 MeRIP-seq:(Medium) rs1172821190 Functional Loss SNV dbSNP153 33..33 33 - - - 108409 RMVar_ID_108409 Human_SNP_ID_621702320 m1A Human chr17 - 30709015 30709015 30709015 GACCGAGCCGGAGCCGGGAACCAGCAATGACAAGCCGCCAGCTCTCCCCTCTCCCCGGCGCACCC GACCGAGCCGGAGCCGGGAACCAGCAATGACACGCCGCCAGCTCTCCCCTCTCCCCGGCGCACCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30709008..30709114 26863196 MeRIP-seq:(Medium) rs1172821190 Functional Loss SNV dbSNP153 33..33 33 - - - 108410 RMVar_ID_108410 Human_SNP_ID_621702326 m1A Human chr17 - 30709021 30709021 30709021 CGCGCGGACCGAGCCGGAGCCGGGAACCAGCAATGACAAGCCGCCAGCTCTCCCCTCTCCCCGGC CGCGCGGACCGAGCCGGAGCCGGGAACCAGCAGTGACAAGCCGCCAGCTCTCCCCTCTCCCCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30709014..30709086 26863196 MeRIP-seq:(Medium) rs1475239705 Functional Loss SNV dbSNP153 33..33 33 - - - 108411 RMVar_ID_108411 Human_SNP_ID_621702350 m1A Human chr17 - 30709079 30709079 30709079 AGAGGGGCGGCGCGGCCGGAGGGGGGGGCGCCAGGCCGGGCCCGTGGGCACCGCAGGACGCGCGG AGAGGGGCGGCGCGGCCGGAGGGGGGGGCGCCGGGCCGGGCCCGTGGGCACCGCAGGACGCGCGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30709037..30709108 26863196 MeRIP-seq:(Medium) rs1431064992 Functional Loss SNV dbSNP153 33..33 33 - - - 108412 RMVar_ID_108412 Human_SNP_ID_621702505 m1A Human chr17 + 30709471 30709471 30709471 CGCTCCGCCTCGCCCCAGCCCCCGGCGCTCTGACGCCGCCCCCGCCCCACAGCCTCCCTCCCCGG CGCTCCGCCTCGCCCCAGCCCCCGGCGCTCTGCCGCCGCCCCCGCCCCACAGCCTCCCTCCCCGG A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:30709372..30709474 32194978 MeRIP-seq:(Medium) rs1432495497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 108413 RMVar_ID_108413 Human_SNP_ID_621702529 m1A Human chr17 - 30709521 30709521 30709521 CTCGCGGCGGCGGAGGCTCGGGACTGGGGGCGATCGGGTCTGCGCCCCTCCCGGGGAGGGAGGCT CTCGCGGCGGCGGAGGCTCGGGACTGGGGGCGGTCGGGTCTGCGCCCCTCCCGGGGAGGGAGGCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:30709443..30709542 26863410 MeRIP-seq:(Medium) rs902136985 Functional Loss SNV dbSNP153 33..33 33 - - - 108414 RMVar_ID_108414 Human_SNP_ID_621708643 m1A Human chr17 + 30731869 30731869 30731869 CCGGGGCCGCCCGGCGAGTAGCTGGCCGGGGAAGGAGGCAGGAACCGCGATGGCGCCTCAGAAGC CCGGGGCCGCCCGGCGAGTAGCTGGCCGGGGAGGGAGGCAGGAACCGCGATGGCGCCTCAGAAGC A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30709695..30731988 26863196 MeRIP-seq:(Medium) rs1262297792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5578602,Human_RBP_ID_8193272,Human_RBP_ID_8254246,Human_RBP_ID_9422821,Human_RBP_ID_17129565,Human_RBP_ID_17379540,Human_RBP_ID_17495311,Human_RBP_ID_18459588,Human_RBP_ID_18486472,Human_RBP_ID_22062068,Human_RBP_ID_26781166,Human_RBP_ID_27838416 Human_miRNA_ID_2917538,Human_miRNA_ID_2917539,Human_miRNA_ID_2917540 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_126544,RMVar_hsa_circ_183252,RMVar_hsa_circ_89901,RMVar_hsa_circ_183251 108415 RMVar_ID_108415 Human_SNP_ID_621708709 m1A Human chr17 + 30732024 30732024 30732024 AATCCGGCGGCGGGGGCTGTGGAGGCGGTGGCAGTTACTCGGCCTCCTCCTCCTCCGCGGCGTTA AATCCGGCGGCGGGGGCTGTGGAGGCGGTGGCGGTTACTCGGCCTCCTCCTCCTCCGCGGCGTTA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30731974..30732078 26863196 MeRIP-seq:(Medium) rs897654174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6764,Human_RBP_ID_3541656,Human_RBP_ID_3950344,Human_RBP_ID_4467210,Human_RBP_ID_5260522,Human_RBP_ID_5578603,Human_RBP_ID_8448750,Human_RBP_ID_18486474,Human_RBP_ID_18693613,Human_RBP_ID_20198403,Human_RBP_ID_22211846,Human_RBP_ID_23118879,Human_RBP_ID_24416386,Human_RBP_ID_26781167 Human_Splice_Rec_1800713,Human_Splice_Rec_1800723 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_126544,RMVar_hsa_circ_183252,RMVar_hsa_circ_89901,RMVar_hsa_circ_183251 108416 RMVar_ID_108416 Human_SNP_ID_621732190 m1A Human chr17 - 30804103 30804103 30804103 TTTGAGTATTTTGTTATTTCTTTTTAGATCAAAGAAAGTGCATCACAGACAAGGGATGTTCTCAA TTTGAGTATTTTGTTATTTCTTTTTAGATCAACGAAAGTGCATCACAGACAAGGGATGTTCTCAA T G CRLF3 Ensembl:ENSG00000176390 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30803993..30809594 26863196 MeRIP-seq:(Medium) rs527256643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1530980,Human_RBP_ID_4417312,Human_RBP_ID_6579258,Human_RBP_ID_22656091 Human_Splice_Rec_1800780,Human_Splice_Rec_1800804 RMVar_hsa_circ_106638,RMVar_hsa_circ_183266,RMVar_hsa_circ_296154,RMVar_hsa_circ_275967,RMVar_hsa_circ_183269,RMVar_hsa_circ_331369,RMVar_hsa_circ_183273,RMVar_hsa_circ_338834,RMVar_hsa_circ_301045,RMVar_hsa_circ_183274,RMVar_hsa_circ_275813 108417 RMVar_ID_108417 Human_SNP_ID_621737324 m1A Human chr17 - 30824635 30824635 30824635 CCGGCCGCGCGGCCAGATGAGGGGGGCGATGGAGCTGGAGCCTGAGCTGCTGTTGCAGGAGGCCC CCGGCCGCGCGGCCAGATGAGGGGGGCGATGGGGCTGGAGCCTGAGCTGCTGTTGCAGGAGGCCC T C CRLF3 Ensembl:ENSG00000176390 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30824020..30824700 26863196 MeRIP-seq:(Medium) rs1161938000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765014,Human_RBP_ID_4465273,Human_RBP_ID_6579339,Human_RBP_ID_18419572 RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 108418 RMVar_ID_108418 Human_SNP_ID_621737349 m1A Human chr17 - 30824653 30824653 30824653 AACCCGCGCTAGGTTTCGCCGGCCGCGCGGCCAGATGAGGGGGGCGATGGAGCTGGAGCCTGAGC AACCCGCGCTAGGTTTCGCCGGCCGCGCGGCCGGATGAGGGGGGCGATGGAGCTGGAGCCTGAGC T C CRLF3 Ensembl:ENSG00000176390 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:30824017..30824730;chr17:30824395..30824682 26863196 MeRIP-seq:(Medium) rs1223124695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465273,Human_RBP_ID_18419572 RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 108419 RMVar_ID_108419 Human_SNP_ID_621756386 m1A Human chr17 - 30899612 30899605 30899612 ATTATTTCTGTTCCTTTATTTTGTCTTTTTTTAAAAAGATTTCCTCGATCATTTCAAAGATGCCT ATTATTTCTGTTCCTTTATTTTGTCTTTTTTT_______TTTCCTCGATCATTTCAAAGATGCCT ATCTTTTT A TEFM Ensembl:ENSG00000172171 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1158521931 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_2501012,Human_RBP_ID_3518401,Human_RBP_ID_6579751,Human_RBP_ID_12958754,Human_RBP_ID_17490220,Human_RBP_ID_25267587 RMVar_hsa_circ_183298,RMVar_hsa_circ_117801,RMVar_hsa_circ_94342,RMVar_hsa_circ_183297 108420 RMVar_ID_108420 Human_SNP_ID_621756394 m1A Human chr17 - 30899612 30899612 30899612 ATTATTTCTGTTCCTTTATTTTGTCTTTTTTTAAAAAGATTTCCTCGATCATTTCAAAGATGCCT ATTATTTCTGTTCCTTTATTTTGTCTTTTTTTTAAAAGATTTCCTCGATCATTTCAAAGATGCCT T A TEFM Ensembl:ENSG00000172171 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28539246 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_2501012,Human_RBP_ID_3518401,Human_RBP_ID_6579751,Human_RBP_ID_12958754,Human_RBP_ID_17490220,Human_RBP_ID_25267587 GWAS_ID_15208,GWAS_ID_15209 RMVar_hsa_circ_183298,RMVar_hsa_circ_117801,RMVar_hsa_circ_94342,RMVar_hsa_circ_183297 108421 RMVar_ID_108421 Human_SNP_ID_621758204 m1A Human chr17 - 30906798 30906798 30906798 CCCTTTATCCCTTCTAAGAGGAATACCGCTCCAGCGCCAACGCAATCTCCTCCTCCCTCGCCTTT CCCTTTATCCCTTCTAAGAGGAATACCGCTCCGGCGCCAACGCAATCTCCTCCTCCCTCGCCTTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30906721..30906838 26863196 MeRIP-seq:(Medium) rs1048645919 Functional Loss SNV dbSNP153 33..33 33 - - - 108422 RMVar_ID_108422 Human_SNP_ID_621774070 m1A Human chr17 + 30971074 30971074 30971074 CCCGACGTCCGCGCCCCGGCCGCCTGTTGGCCATGGCGGGCCTGGGCCTGGGCTCCGCCGTTCCC CCCGACGTCCGCGCCCCGGCCGCCTGTTGGCCGTGGCGGGCCTGGGCCTGGGCTCCGCCGTTCCC A G RNF135 Ensembl:ENSG00000181481 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30971031..30971176 26863196 MeRIP-seq:(Medium) rs1057049231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4417622 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 108423 RMVar_ID_108423 Human_SNP_ID_621774071 m1A Human chr17 + 30971074 30971074 30971074 CCCGACGTCCGCGCCCCGGCCGCCTGTTGGCCATGGCGGGCCTGGGCCTGGGCTCCGCCGTTCCC CCCGACGTCCGCGCCCCGGCCGCCTGTTGGCCTTGGCGGGCCTGGGCCTGGGCTCCGCCGTTCCC A T RNF135 Ensembl:ENSG00000181481 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:30971031..30971176 26863196 MeRIP-seq:(Medium) rs1057049231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4417622 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 108424 RMVar_ID_108424 Human_SNP_ID_621774115 m1A Human chr17 - 30971129 30971129 30971129 AGTCCAGCAGCCCCTGGCAGATGATGCAGCCGAGGTCGTCCTCGGCCAGCCACACGGGAACGGCG AGTCCAGCAGCCCCTGGCAGATGATGCAGCCGGGGTCGTCCTCGGCCAGCCACACGGGAACGGCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30971081..30971171 26863196 MeRIP-seq:(Medium) rs994968398 Functional Loss SNV dbSNP153 33..33 33 - - - 108425 RMVar_ID_108425 Human_SNP_ID_621774259 m1A Human chr17 + 30971363 30971363 30971363 CCGCGCCGCACGCGAGATACAGGCGGGCTCCGACCCTGCCCACTGCCCCTGCCCGGGCTCCAGTT CCGCGCCGCACGCGAGATACAGGCGGGCTCCGCCCCTGCCCACTGCCCCTGCCCGGGCTCCAGTT A C RNF135 Ensembl:ENSG00000181481 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:30971315..30971476 26863196 MeRIP-seq:(Medium) rs1281959387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1801045,Human_Splice_Rec_1801049,Human_Splice_Rec_1801055,Human_Splice_Rec_1801063,Human_Splice_Rec_1801073 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 108426 RMVar_ID_108426 Human_SNP_ID_621782128 m1A Human chr17 + 30999033 30999033 30999033 CAGACAGACCTGGGGTGGTGGGCATCTGGCTGAACCTTGAGGAGGGAAAGCTTGCCTTCTATTCA CAGACAGACCTGGGGTGGTGGGCATCTGGCTGGACCTTGAGGAGGGAAAGCTTGCCTTCTATTCA A G RNF135 Ensembl:ENSG00000181481 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30998982..30999067 26863196 MeRIP-seq:(Medium) rs956240623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_109750,RMVar_hsa_circ_75761,RMVar_hsa_circ_85921,RMVar_hsa_circ_183301,RMVar_hsa_circ_183302,RMVar_hsa_circ_82150,RMVar_hsa_circ_183303,RMVar_hsa_circ_183304 108427 RMVar_ID_108427 Human_SNP_ID_621803729 m1A Human chr17 - 31095011 31095011 31095011 CCCCACTAGCGCCGTCTCCCCACAGCCATCACAGTCCGAGACGCCGCCATGACACCCCACCGGAA CCCCACTAGCGCCGTCTCCCCACAGCCATCACGGTCCGAGACGCCGCCATGACACCCCACCGGAA T C AC138207.2 Ensembl:ENSG00000264107 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:31094962..31095051 26863196 MeRIP-seq:(Medium) rs987981455 Functional Loss SNV dbSNP153 33..33 33 - - - 108428 RMVar_ID_108428 Human_SNP_ID_621803730 m1A Human chr17 - 31095013 31095013 31095013 CTCCCCACTAGCGCCGTCTCCCCACAGCCATCACAGTCCGAGACGCCGCCATGACACCCCACCGG CTCCCCACTAGCGCCGTCTCCCCACAGCCATCGCAGTCCGAGACGCCGCCATGACACCCCACCGG T C AC138207.2 Ensembl:ENSG00000264107 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:31094962..31095054 26863196 MeRIP-seq:(Medium) rs1020754650 Functional Loss SNV dbSNP153 33..33 33 - - - 108429 RMVar_ID_108429 Human_SNP_ID_621803827 m1A Human chr17 - 31095234 31095234 31095234 GCGCCCTGGGCCGGGAAGAGGGCGGGGAGCGGAGGCTGAGGTGAGGGAAGAGGCAAGGAGAGGGT GCGCCCTGGGCCGGGAAGAGGGCGGGGAGCGGGGGCTGAGGTGAGGGAAGAGGCAAGGAGAGGGT T C AC138207.2 Ensembl:ENSG00000264107 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:31093468..31095401 32194978 MeRIP-seq:(Medium) rs1386772134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1801139 108430 RMVar_ID_108430 Human_SNP_ID_621803849 m1A Human chr17 - 31095282 31095282 31095282 GCCATGTCCTCCCCGCGGCCGGGGGGCGGCGGAGGGAAGGGTGGGCCGGCGCCCTGGGCCGGGAA GCCATGTCCTCCCCGCGGCCGGGGGGCGGCGGTGGGAAGGGTGGGCCGGCGCCCTGGGCCGGGAA T A AC138207.2 Ensembl:ENSG00000264107 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:31095253..31095352 26863196 MeRIP-seq:(Medium) rs756130588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1801139 108431 RMVar_ID_108431 Human_SNP_ID_621810386 m1A Human chr17 + 31122195 31122195 31122195 AAGAAATTGTTATAATAGGGATGATCTGAGCCAGGGTACTCATTATAGGAAATTAGGGGCAACCT AAGAAATTGTTATAATAGGGATGATCTGAGCCGGGGTACTCATTATAGGAAATTAGGGGCAACCT A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:31122161..31122298 26863196 MeRIP-seq:(Medium) rs939088464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12959503,Human_RBP_ID_17128685 RMVar_hsa_circ_183307,RMVar_hsa_circ_95146 108432 RMVar_ID_108432 Human_SNP_ID_621914975 m1A Human chr17 + 31549480 31549480 31549480 AAGGTCGTGCTTCGTGCAGGGCCAGCGAGGGAAGGTCACCTCCCGGCGCCCCGAGCCTGGCCCCA AAGGTCGTGCTTCGTGCAGGGCCAGCGAGGGACGGTCACCTCCCGGCGCCCCGAGCCTGGCCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:31549135..31549938 26863196 MeRIP-seq:(Medium) rs1353901973 Functional Loss SNV dbSNP153 33..33 33 - - - 108433 RMVar_ID_108433 Human_SNP_ID_621915327 m1A Human chr17 - 31550171 31550171 31550171 GACGGCGTACGTGGAGAAAACCCGACTTCCCCACAGCCAAAGCCCTACCTCGGGTCTCAGGCACG GACGGCGTACGTGGAGAAAACCCGACTTCCCCGCAGCCAAAGCCCTACCTCGGGTCTCAGGCACG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:31550074..31550230 26863196 MeRIP-seq:(Medium) rs1000722395 Functional Loss SNV dbSNP153 33..33 33 - - - 108434 RMVar_ID_108434 Human_SNP_ID_621915330 m1A Human chr17 + 31550176 31550176 31550176 CTGAGACCCGAGGTAGGGCTTTGGCTGTGGGGAAGTCGGGTTTTCTCCACGTACGCCGTCCCTTC CTGAGACCCGAGGTAGGGCTTTGGCTGTGGGGGAGTCGGGTTTTCTCCACGTACGCCGTCCCTTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:31550087..31550225 26863196 MeRIP-seq:(Medium) rs1203573349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_278103,Human_RBP_ID_1181155,Human_RBP_ID_1285617,Human_RBP_ID_1367773,Human_RBP_ID_1531200,Human_RBP_ID_1854472,Human_RBP_ID_2501561,Human_RBP_ID_3519036,Human_RBP_ID_5259988,Human_RBP_ID_5274899,Human_RBP_ID_6581477,Human_RBP_ID_8449182,Human_RBP_ID_8816192,Human_RBP_ID_12962560,Human_RBP_ID_17691714,Human_RBP_ID_18694148,Human_RBP_ID_20200962,Human_RBP_ID_22803897,Human_RBP_ID_23129067,Human_RBP_ID_23720510,Human_RBP_ID_24415044,Human_RBP_ID_24478383,Human_RBP_ID_27450902 108435 RMVar_ID_108435 Human_SNP_ID_621915331 m1A Human chr17 + 31550177 31550177 31550177 TGAGACCCGAGGTAGGGCTTTGGCTGTGGGGAAGTCGGGTTTTCTCCACGTACGCCGTCCCTTCT TGAGACCCGAGGTAGGGCTTTGGCTGTGGGGAGGTCGGGTTTTCTCCACGTACGCCGTCCCTTCT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:31550076..31550266 26863196 MeRIP-seq:(Medium) rs1270057871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_278103,Human_RBP_ID_1181155,Human_RBP_ID_1285617,Human_RBP_ID_1367773,Human_RBP_ID_1531200,Human_RBP_ID_1854472,Human_RBP_ID_2501561,Human_RBP_ID_3519036,Human_RBP_ID_5259988,Human_RBP_ID_5274899,Human_RBP_ID_6581477,Human_RBP_ID_8449182,Human_RBP_ID_8816192,Human_RBP_ID_12962560,Human_RBP_ID_17691714,Human_RBP_ID_18694148,Human_RBP_ID_20200962,Human_RBP_ID_22803897,Human_RBP_ID_23129067,Human_RBP_ID_23720510,Human_RBP_ID_24415044,Human_RBP_ID_24478383,Human_RBP_ID_27252452,Human_RBP_ID_27450902 108436 RMVar_ID_108436 Human_SNP_ID_621915332 m1A Human chr17 - 31550179 31550179 31550179 GTAGAAGGGACGGCGTACGTGGAGAAAACCCGACTTCCCCACAGCCAAAGCCCTACCTCGGGTCT GTAGAAGGGACGGCGTACGTGGAGAAAACCCGGCTTCCCCACAGCCAAAGCCCTACCTCGGGTCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:31550108..31550209 26863196 MeRIP-seq:(Medium) rs974790993 Functional Loss SNV dbSNP153 33..33 33 - - - 108437 RMVar_ID_108437 Human_SNP_ID_621919580 m1A Human chr17 + 31566060 31566060 31566060 GGGTTGGGTTCATGCGGCCGCCACTTAAGCCTATCTGAGGGGAGAGGTTAGTGGGAGAGTCAGGA GGGTTGGGTTCATGCGGCCGCCACTTAAGCCTGTCTGAGGGGAGAGGTTAGTGGGAGAGTCAGGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:31565985..31566090 26863196 MeRIP-seq:(Medium) rs1438325872 Functional Loss SNV dbSNP153 33..33 33 - - - 108438 RMVar_ID_108438 Human_SNP_ID_621992238 m1A Human chr17 + 31856859 31856859 31856859 TCTCTCCTGACTGGAGTGGTCAGCTGTAGCAAAGCCAGCCTGCAGGAAGAAGAAATGATTACCAA TCTCTCCTGACTGGAGTGGTCAGCTGTAGCAACGCCAGCCTGCAGGAAGAAGAAATGATTACCAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:31856801..31858818 32194978 MeRIP-seq:(Medium) rs200939865 Functional Loss SNV dbSNP153 33..33 33 - - - 108439 RMVar_ID_108439 Human_SNP_ID_621992812 m1A Human chr17 - 31859156 31859156 31859156 GGCCGCCGGGGCCCAGGCGCAGGGGGCCGCGGAGCCGTCTCGGGGCCCGCCGCTGCCTAGCGCGC GGCCGCCGGGGCCCAGGCGCAGGGGGCCGCGGCGCCGTCTCGGGGCCCGCCGCTGCCTAGCGCGC T G COPRS Ensembl:ENSG00000172301 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr17:31858722..31859300;chr17:31859063..31859225 26863196,32194978 MeRIP-seq:(Medium) rs1378951895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4418169,Human_RBP_ID_22499142 Human_Splice_Rec_1802035,Human_Splice_Rec_1802039,Human_Splice_Rec_1802045 108440 RMVar_ID_108440 Human_SNP_ID_622003838 m1A Human chr17 + 31901602 31901602 31901602 CCAGCTGTTCCAATTCCGGGAGCCGATCTTCTATGCGTTCCTGAATTATCTCTGCCATGAGGTCC CCAGCTGTTCCAATTCCGGGAGCCGATCTTCTCTGCGTTCCTGAATTATCTCTGCCATGAGGTCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:31901551..31901704 26863196 MeRIP-seq:(Medium) rs541116440 Functional Loss SNV dbSNP153 33..33 33 - - - 108441 RMVar_ID_108441 Human_SNP_ID_622003839 m1A Human chr17 + 31901602 31901602 31901602 CCAGCTGTTCCAATTCCGGGAGCCGATCTTCTATGCGTTCCTGAATTATCTCTGCCATGAGGTCC CCAGCTGTTCCAATTCCGGGAGCCGATCTTCTGTGCGTTCCTGAATTATCTCTGCCATGAGGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:31901551..31901704 26863196 MeRIP-seq:(Medium) rs541116440 Functional Loss SNV dbSNP153 33..33 33 - - - 108442 RMVar_ID_108442 Human_SNP_ID_622003844 m1A Human chr17 - 31901616 31901616 31901616 GGGTTGTAGACCTCGGACCTCATGGCAGAGATAATTCAGGAACGCATAGAAGATCGGCTCCCGGA GGGTTGTAGACCTCGGACCTCATGGCAGAGATCATTCAGGAACGCATAGAAGATCGGCTCCCGGA T G UTP6 Ensembl:ENSG00000108651 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:31901565..31901709 26863196 MeRIP-seq:(Medium) rs753130831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1854530,Human_RBP_ID_4465277,Human_RBP_ID_5577078,Human_RBP_ID_8232341,Human_RBP_ID_9375672,Human_RBP_ID_12963491,Human_RBP_ID_18419573,Human_RBP_ID_22959790,Human_RBP_ID_26330687,Human_RBP_ID_27812523 Human_Splice_Rec_1802053,Human_Splice_Rec_1802131,Human_Splice_Rec_1802169 108443 RMVar_ID_108443 Human_SNP_ID_622013352 m1A Human chr17 - 31937319 31937319 31937319 CGTCGCCGCCGCCACCGCCGCCGAACCCCCGAAGCCGCCTCCCCCGGACCCCGCGCTGGGCCCCG CGTCGCCGCCGCCACCGCCGCCGAACCCCCGAGGCCGCCTCCCCCGGACCCCGCGCTGGGCCCCG T C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,H2O2 treatment;HEPG2 cell line,mRNA untreated chr17:31937217..31937318;chr17:31937032..31937318 26863410,26863196 MeRIP-seq:(Medium) rs1161554779 Functional Loss SNV dbSNP153 33..33 33 - - - 108444 RMVar_ID_108444 Human_SNP_ID_622013366 m1A Human chr17 + 31937349 31937340 31937349 GCTTCGGGGGTTCGGCGGCGGTGGCGGCGGCGACGGCTTCGGGCGGCAAATCCGGCGGCGGGAGC GCTTCGGGGGTTCGGCGGCGGTGG_________CGGCTTCGGGCGGCAAATCCGGCGGCGGGAGC GCGGCGGCGA G SUZ12 Ensembl:ENSG00000178691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:31937049..31937468;chr17:31937167..31937434;chr17:31937267..31937464 26863196 MeRIP-seq:(Medium) rs1384625638 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_236898,Human_RBP_ID_766369,Human_RBP_ID_820387,Human_RBP_ID_3542839,Human_RBP_ID_3952126,Human_RBP_ID_5088296,Human_RBP_ID_5185138,Human_RBP_ID_5318365,Human_RBP_ID_5364014,Human_RBP_ID_9341009,Human_RBP_ID_9422288,Human_RBP_ID_18459592,Human_RBP_ID_18990933,Human_RBP_ID_19085086,Human_RBP_ID_21974284,Human_RBP_ID_22062071,Human_RBP_ID_22212034,Human_RBP_ID_26781169,Human_RBP_ID_26958671,Human_RBP_ID_27838422 RMVar_hsa_circ_107506,RMVar_hsa_circ_119148,RMVar_hsa_circ_183430,RMVar_hsa_circ_183431 108445 RMVar_ID_108445 Human_SNP_ID_622013371 m1A Human chr17 + 31937349 31937349 31937349 GCTTCGGGGGTTCGGCGGCGGTGGCGGCGGCGACGGCTTCGGGCGGCAAATCCGGCGGCGGGAGC GCTTCGGGGGTTCGGCGGCGGTGGCGGCGGCGGCGGCTTCGGGCGGCAAATCCGGCGGCGGGAGC A G SUZ12 Ensembl:ENSG00000178691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:31937049..31937468;chr17:31937167..31937434;chr17:31937267..31937464 26863196 MeRIP-seq:(Medium) rs1224696424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236898,Human_RBP_ID_766369,Human_RBP_ID_820387,Human_RBP_ID_3542839,Human_RBP_ID_3952126,Human_RBP_ID_5088296,Human_RBP_ID_5185138,Human_RBP_ID_5318365,Human_RBP_ID_5364014,Human_RBP_ID_9341009,Human_RBP_ID_9422288,Human_RBP_ID_18459592,Human_RBP_ID_18990933,Human_RBP_ID_19085086,Human_RBP_ID_21974284,Human_RBP_ID_22062071,Human_RBP_ID_22212034,Human_RBP_ID_26781169,Human_RBP_ID_26958671,Human_RBP_ID_27838422 RMVar_hsa_circ_107506,RMVar_hsa_circ_119148,RMVar_hsa_circ_183430,RMVar_hsa_circ_183431 108446 RMVar_ID_108446 Human_SNP_ID_622032771 m1A Human chr17 + 32007998 32007998 32007998 GGAGTAAGAGGAGGGGGGCGGCGATGCCGAGGAGACCCAGGAGTCTGAGGACAACTAGGAGGATG GGAGTAAGAGGAGGGGGGCGGCGATGCCGAGGGGACCCAGGAGTCTGAGGACAACTAGGAGGATG A G LRRC37B Ensembl:ENSG00000185158 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:32007791..32008064 26863196 MeRIP-seq:(Medium) rs1262760836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5319002,Human_RBP_ID_22959205 108447 RMVar_ID_108447 Human_SNP_ID_622040261 m1A Human chr17 - 32040393 32040393 32040393 CGCCGCAGAACCTCCGCCCGGACCGTGCCAGCAACAGGCTCCCAGGTGCGTGACCCTCTGCACGC CGCCGCAGAACCTCCGCCCGGACCGTGCCAGCGACAGGCTCCCAGGTGCGTGACCCTCTGCACGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32040342..32040563 26863196 MeRIP-seq:(Medium) rs1028671336 Functional Loss SNV dbSNP153 33..33 33 - - - 108448 RMVar_ID_108448 Human_SNP_ID_622065340 m1A Human chr17 + 32142504 32142477 32142504 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACAGCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC GCCGCC___________________________GCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC CGCCGCCGCCGCCGCCGCCGCCGCCACA C RHOT1 Ensembl:ENSG00000126858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:32142424..32142524 26863196 MeRIP-seq:(Medium) rs1182701982 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_8825423 RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 108449 RMVar_ID_108449 Human_SNP_ID_622065379 m1A Human chr17 + 32142504 32142498 32142504 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACAGCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC GCCGCCGCCGCCGCCGCCGCCGCCGCC______GCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC CGCCACA C RHOT1 Ensembl:ENSG00000126858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:32142424..32142524 26863196 MeRIP-seq:(Medium) rs1269469468 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_8825423 RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 108450 RMVar_ID_108450 Human_SNP_ID_622065385 m1A Human chr17 + 32142504 32142501 32142504 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACAGCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC GCCGCCGCCGCCGCCGCCGCCGCCGCCGCC___GCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC CACA C RHOT1 Ensembl:ENSG00000126858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:32142424..32142524 26863196 MeRIP-seq:(Medium) rs1179673176 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8825423 RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 108451 RMVar_ID_108451 Human_SNP_ID_622065388 m1A Human chr17 + 32142504 32142504 32142504 GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACAGCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGCTGGGCCGGAGGAGGCGGAGCTGGCGC A C RHOT1 Ensembl:ENSG00000126858 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:32142424..32142524 26863196 MeRIP-seq:(Medium) rs1304299452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8825423 RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 108452 RMVar_ID_108452 Human_SNP_ID_622112476 m1A Human chr17 + 32330023 32330023 32330023 TGCCACAGTTCCCAGCTAATTTTTGTAATTTTAGTAGAGACAGGGTTTCACCATATTGGTCAGGC TGCCACAGTTCCCAGCTAATTTTTGTAATTTTGGTAGAGACAGGGTTTCACCATATTGGTCAGGC A G AC005899.5 Ensembl:ENSG00000265794 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:32329942..32330026 26863410 MeRIP-seq:(Medium) rs1002561352 Functional Loss SNV dbSNP153 33..33 33 - - - 108453 RMVar_ID_108453 Human_SNP_ID_622115220 m1A Human chr17 + 32341825 32341825 32341825 AGGCATACAAGTCCACGACGGGGGCCAGGAAGAGCAGCGGGAGGCGAGGAGCGCCCTTCAGGCCA AGGCATACAAGTCCACGACGGGGGCCAGGAAGGGCAGCGGGAGGCGAGGAGCGCCCTTCAGGCCA A G AC005899.5 Ensembl:ENSG00000265794 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:32341822..32341888 26863196 MeRIP-seq:(Medium) rs1204840569 Functional Loss SNV dbSNP153 33..33 33 - - - 108454 RMVar_ID_108454 Human_SNP_ID_622115221 m1A Human chr17 + 32341825 32341825 32341825 AGGCATACAAGTCCACGACGGGGGCCAGGAAGAGCAGCGGGAGGCGAGGAGCGCCCTTCAGGCCA AGGCATACAAGTCCACGACGGGGGCCAGGAAGTGCAGCGGGAGGCGAGGAGCGCCCTTCAGGCCA A T AC005899.5 Ensembl:ENSG00000265794 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:32341822..32341888 26863196 MeRIP-seq:(Medium) rs1204840569 Functional Loss SNV dbSNP153 33..33 33 - - - 108455 RMVar_ID_108455 Human_SNP_ID_622115321 m1A Human chr17 - 32342095 32342095 32342095 TTGCAGGAGTCGATGGATGGAGATGAAAAGGAACTAGAGAGCAGCGAAGAGGGAGGCTCAGCCGA TTGCAGGAGTCGATGGATGGAGATGAAAAGGATCTAGAGAGCAGCGAAGAGGGAGGCTCAGCCGA T A C17orf75 Ensembl:ENSG00000108666 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32342044..32342139 26863196 MeRIP-seq:(Medium) rs1216594067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1531387,Human_RBP_ID_4465280,Human_RBP_ID_9377892 Human_Splice_Rec_1802973,Human_Splice_Rec_1802989,Human_Splice_Rec_1803022,Human_Splice_Rec_1803023,Human_Splice_Rec_1803051,Human_Splice_Rec_1803070,Human_Splice_Rec_1803071,Human_Splice_Rec_1803077,Human_Splice_Rec_1803083 108456 RMVar_ID_108456 Human_SNP_ID_622115332 m1A Human chr17 - 32342123 32342123 32342123 CTCAGAGGCCGCCGCAATGCTCCCCTCTTTGCAGGAGTCGATGGATGGAGATGAAAAGGAACTAG CTCAGAGGCCGCCGCAATGCTCCCCTCTTTGCTGGAGTCGATGGATGGAGATGAAAAGGAACTAG T A C17orf75 Ensembl:ENSG00000108666 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:32341968..32342150 26863196 MeRIP-seq:(Medium) rs754516765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465280,Human_RBP_ID_18694357 108457 RMVar_ID_108457 Human_SNP_ID_622115333 m1A Human chr17 - 32342123 32342123 32342123 CTCAGAGGCCGCCGCAATGCTCCCCTCTTTGCAGGAGTCGATGGATGGAGATGAAAAGGAACTAG CTCAGAGGCCGCCGCAATGCTCCCCTCTTTGCGGGAGTCGATGGATGGAGATGAAAAGGAACTAG T C C17orf75 Ensembl:ENSG00000108666 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:32341968..32342150 26863196 MeRIP-seq:(Medium) rs754516765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465280,Human_RBP_ID_18694357 108458 RMVar_ID_108458 Human_SNP_ID_622118079 m1A Human chr17 + 32351722 32351722 32351722 GTTTTAGCTGTTCCCATATTGTAATGTTATCCATATGTTTTTATTATAGGCAGTGTCATCATTAG GTTTTAGCTGTTCCCATATTGTAATGTTATCCGTATGTTTTTATTATAGGCAGTGTCATCATTAG A G ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:32351715..32351825 26863410 MeRIP-seq:(Medium) rs757335879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2501834,Human_RBP_ID_6582392,Human_RBP_ID_12965833,Human_RBP_ID_17609567 108459 RMVar_ID_108459 Human_SNP_ID_622118080 m1A Human chr17 - 32351725 32351725 32351725 AGCCTAATGATGACACTGCCTATAATAAAAACATATGGATAACATTACAATATGGGAACAGCTAA AGCCTAATGATGACACTGCCTATAATAAAAACGTATGGATAACATTACAATATGGGAACAGCTAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32351723..32351825 26863196 MeRIP-seq:(Medium) rs767553224 Functional Loss SNV dbSNP153 33..33 33 - - - 108460 RMVar_ID_108460 Human_SNP_ID_622123387 m1A Human chr17 + 32367878 32367878 32367878 ACCCCCAAAGCCTACATTCCCTGCTTATACACAGTCTACAGCTTCAACAACTAGTACAACAAATA ACCCCCAAAGCCTACATTCCCTGCTTATACACTGTCTACAGCTTCAACAACTAGTACAACAAATA A T ZNF207 Ensembl:ENSG00000010244 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32367827..32367911 26863196 MeRIP-seq:(Medium) rs201526862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46750,Human_RBP_ID_764278,Human_RBP_ID_1531427,Human_RBP_ID_1854806,Human_RBP_ID_3519355,Human_RBP_ID_9287197,Human_RBP_ID_17259072,Human_RBP_ID_17375007,Human_RBP_ID_17490364,Human_RBP_ID_18530573,Human_RBP_ID_18694414,Human_RBP_ID_22212130,Human_RBP_ID_22803938,Human_RBP_ID_24415066,Human_RBP_ID_25340417 Human_miRNA_ID_2088317,Human_miRNA_ID_2977697 RMVar_hsa_circ_62414,RMVar_hsa_circ_114825,RMVar_hsa_circ_183528,RMVar_hsa_circ_183537,RMVar_hsa_circ_117121,RMVar_hsa_circ_273747,RMVar_hsa_circ_324913,RMVar_hsa_circ_267737,RMVar_hsa_circ_272522,RMVar_hsa_circ_109828,RMVar_hsa_circ_183534,RMVar_hsa_circ_183535,RMVar_hsa_circ_183533,RMVar_hsa_circ_354356,RMVar_hsa_circ_91275,RMVar_hsa_circ_107593,RMVar_hsa_circ_183536,RMVar_hsa_circ_183538,RMVar_hsa_circ_99351,RMVar_hsa_circ_337239,RMVar_hsa_circ_183539 108461 RMVar_ID_108461 Human_SNP_ID_622147193 m1A Human chr17 + 32460814 32460814 32460814 CTAGAGAACCATCTTCAGCTTGCTATTCCCAAAGTTGGTATGATTCAGGTTATGATCTGTTCATT CTAGAGAACCATCTTCAGCTTGCTATTCCCAAGGTTGGTATGATTCAGGTTATGATCTGTTCATT A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:32460809..32460956 26863196 MeRIP-seq:(Medium) rs887090206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20140,RMVar_hsa_circ_302442,RMVar_hsa_circ_320735,RMVar_hsa_circ_342095,RMVar_hsa_circ_363479,RMVar_hsa_circ_348967,RMVar_hsa_circ_331325,RMVar_hsa_circ_304905,RMVar_hsa_circ_183545,RMVar_hsa_circ_183546,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544 108462 RMVar_ID_108462 Human_SNP_ID_622152098 m1A Human chr17 + 32481351 32481351 32481351 AAGGTCCTGCCGCCGCCGCCACCACCACCACCACTGCAGCAACAACAGCAGCAGCAGCAGCAGCG AAGGTCCTGCCGCCGCCGCCACCACCACCACCGCTGCAGCAACAACAGCAGCAGCAGCAGCAGCG A G PSMD11 Ensembl:ENSG00000108671 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32481301..32481450 26863196 MeRIP-seq:(Medium) rs762328019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237405,Human_RBP_ID_6583490,Human_RBP_ID_20201911 Human_Splice_Rec_1803318 108463 RMVar_ID_108463 Human_SNP_ID_622153565 m1A Human chr17 + 32486856 32486856 32486856 CGACTCCCCGGCGAGACCAGGCCGGAGCGTGGACGGCGCGCGCGCCCCGCGAGGGAGGGCGCTGA CGACTCCCCGGCGAGACCAGGCCGGAGCGTGGCCGGCGCGCGCGCCCCGCGAGGGAGGGCGCTGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32486672..32486982 26863196 MeRIP-seq:(Medium) rs1204716419 Functional Loss SNV dbSNP153 33..33 33 - - - 108464 RMVar_ID_108464 Human_SNP_ID_622153789 m1A Human chr17 - 32487283 32487280 32487283 CGCCCGCCGCCGCCGCTGCGGTCCCCAGGCGCAGCCGGGAGGGGCCCGGTCGCCGACGGAGGCGG CGCCCGCCGCCGCCGCTGCGGTCCCCAGGCGC___CGGGAGGGGCCCGGTCGCCGACGGAGGCGG GGCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:32487235..32487439 26863196 MeRIP-seq:(Medium) rs1177602924 Functional Loss DEL dbSNP153 33..35 33 - - - 108465 RMVar_ID_108465 Human_SNP_ID_622590109 m1A Human chr17 + 34255347 34255347 34255347 ATTCTCAAACTGAAGCTCGCACTCTCGCCTCCAGCATGAAAGTCTCTGCCGCCCTTCTGTGCCTG ATTCTCAAACTGAAGCTCGCACTCTCGCCTCCGGCATGAAAGTCTCTGCCGCCCTTCTGTGCCTG A G CCL2 Ensembl:ENSG00000108691 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:34255297..34255406 26863196 MeRIP-seq:(Medium) rs749900916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1803937,Human_Splice_Rec_1803939 108466 RMVar_ID_108466 Human_SNP_ID_622767641 m1A Human chr17 + 34961604 34961604 34961604 GTCCTCCGCCTCCGCCCGGACTCCGGCAGGGAAGCGAGTGATAAATCAGGAAGAATTGCGGCGGT GTCCTCCGCCTCCGCCCGGACTCCGGCAGGGAGGCGAGTGATAAATCAGGAAGAATTGCGGCGGT A G ZNF830 Ensembl:ENSG00000198783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:34961551..34961743;chr17:34961551..34962228;chr17:34961551..34961909 26863196 MeRIP-seq:(Medium) rs367958595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546647,Human_RBP_ID_4465292,Human_RBP_ID_26331570 108467 RMVar_ID_108467 Human_SNP_ID_622767656 m1A Human chr17 - 34961627 34961627 34961627 CAGACGCTGCTTCTCCTTCATTAACCGCCGCAATTCTTCCTGATTTATCACTCGCTTCCCTGCCG CAGACGCTGCTTCTCCTTCATTAACCGCCGCAGTTCTTCCTGATTTATCACTCGCTTCCCTGCCG T C CCT6B Ensembl:ENSG00000132141 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:34961576..34961795 26863196 MeRIP-seq:(Medium) rs1348708512 Functional Loss SNV dbSNP153 33..33 33 - - - 108468 RMVar_ID_108468 Human_SNP_ID_622767858 m1A Human chr17 + 34962079 34962079 34962079 GATGAGGAGGAGGAGGAAGAGGAGGAGGAAGGAGATGGAGAAAGAAAAAGGGGGGACGCCAGCAA GATGAGGAGGAGGAGGAAGAGGAGGAGGAAGGGGATGGAGAAAGAAAAAGGGGGGACGCCAGCAA A G ZNF830 Ensembl:ENSG00000198783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:34962028..34962179 26863196 MeRIP-seq:(Medium) rs764877793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18694715 108469 RMVar_ID_108469 Human_SNP_ID_622767978 m1A Human chr17 + 34962414 34962414 34962414 AGAGTGGGACGAATTCCAAAAAGCCATGAGGCAGGTCAACACTATTTCCGAAGCCATAGTTGCCG AGAGTGGGACGAATTCCAAAAAGCCATGAGGCCGGTCAACACTATTTCCGAAGCCATAGTTGCCG A C ZNF830 Ensembl:ENSG00000198783 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:34962363..34962628 26863196 MeRIP-seq:(Medium) rs1476101269 Functional Loss SNV dbSNP153 33..33 33 - - - 108470 RMVar_ID_108470 Human_SNP_ID_622768002 m1A Human chr17 + 34962502 34962502 34962502 GACCGCCAGATTGGGGAGATCGATGAGCAGATAGAGTGTTACCGACGGGTGGAAAAGCTACGGAA GACCGCCAGATTGGGGAGATCGATGAGCAGATGGAGTGTTACCGACGGGTGGAAAAGCTACGGAA A G ZNF830 Ensembl:ENSG00000198783 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:34962283..34962628 26863196 MeRIP-seq:(Medium) rs752765946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4471044,Human_RBP_ID_6583981,Human_RBP_ID_26333151,Human_RBP_ID_27813696 108471 RMVar_ID_108471 Human_SNP_ID_622772037 m1A Human chr17 - 34980624 34980624 34980624 CCGCCGCGCCGTGCCGCGCCGCGTAGCCCCTCACCTGCCTCTCCGGCTCCGGCGCTCACCGTAGG CCGCCGCGCCGTGCCGCGCCGCGTAGCCCCTCCCCTGCCTCTCCGGCTCCGGCGCTCACCGTAGG T G CCT6B Ensembl:ENSG00000132141 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:34980585..34980678 26863196 MeRIP-seq:(Medium) rs1044406726 Functional Loss SNV dbSNP153 33..33 33 - - - 108472 RMVar_ID_108472 Human_SNP_ID_622772207 m1A Human chr17 - 34981052 34981052 34981052 GCTTCCCGCGCCGCTGTCGGAGAGTGGCGGGGACAGTGGGGTCGGCGGCGTAGGCCGCGACCCCC GCTTCCCGCGCCGCTGTCGGAGAGTGGCGGGGGCAGTGGGGTCGGCGGCGTAGGCCGCGACCCCC T C CCT6B Ensembl:ENSG00000132141 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:34981050..34981234 26863196 MeRIP-seq:(Medium) rs1345179856 Functional Loss SNV dbSNP153 33..33 33 - - - 108473 RMVar_ID_108473 Human_SNP_ID_622772907 m1A Human chr17 + 34983442 34983442 34983442 AGAGTGGTACCACATTAAATGCATGTTTGAGAAACTAGAGCGGGCCCGGGCCACCACAAAAAAAA AGAGTGGTACCACATTAAATGCATGTTTGAGACACTAGAGCGGGCCCGGGCCACCACAAAAAAAA A C LIG3 Ensembl:ENSG00000005156 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:34983392..34983478 26863196 MeRIP-seq:(Medium) rs1375638775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905208,Human_RBP_ID_12969455 RMVar_hsa_circ_65471,RMVar_hsa_circ_285464,RMVar_hsa_circ_278679,RMVar_hsa_circ_183617,RMVar_hsa_circ_183618,RMVar_hsa_circ_352999 108474 RMVar_ID_108474 Human_SNP_ID_622777471 m1A Human chr17 + 35001975 35001975 35001975 TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCACTACAGGGGGTAGCAGTGAAGAGAATAAGGGT TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCCCTACAGGGGGTAGCAGTGAAGAGAATAAGGGT A C LIG3 Ensembl:ENSG00000005156 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:35001933..35002053 26863196 MeRIP-seq:(Medium) rs1411966445 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_17691769,Human_RBP_ID_17904789,Human_RBP_ID_27812550 Human_Splice_Rec_1804178,Human_Splice_Rec_1804216,Human_Splice_Rec_1804290 RMVar_hsa_circ_92027,RMVar_hsa_circ_115,RMVar_hsa_circ_183623,RMVar_hsa_circ_358905 108475 RMVar_ID_108475 Human_SNP_ID_622777472 m1A Human chr17 + 35001975 35001975 35001975 TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCACTACAGGGGGTAGCAGTGAAGAGAATAAGGGT TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCGCTACAGGGGGTAGCAGTGAAGAGAATAAGGGT A G LIG3 Ensembl:ENSG00000005156 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:35001933..35002053 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_17691769,Human_RBP_ID_17904789,Human_RBP_ID_27812550 Human_Splice_Rec_1804178,Human_Splice_Rec_1804216,Human_Splice_Rec_1804290 RMVar_hsa_circ_92027,RMVar_hsa_circ_115,RMVar_hsa_circ_183623,RMVar_hsa_circ_358905 108476 RMVar_ID_108476 Human_SNP_ID_622805787 m1A Human chr17 + 35119719 35119719 35119719 GCCCCTCCCCTACCCCTTCCTAGAGAGGACACAGGCGCGCTGGCTGCCGGAGGAGAAAGGAGAGA GCCCCTCCCCTACCCCTTCCTAGAGAGGACACCGGCGCGCTGGCTGCCGGAGGAGAAAGGAGAGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:35119675..35119808 26863196 MeRIP-seq:(Medium) rs1285772390 Functional Loss SNV dbSNP153 33..33 33 - - - 108477 RMVar_ID_108477 Human_SNP_ID_622805788 m1A Human chr17 + 35119719 35119719 35119719 GCCCCTCCCCTACCCCTTCCTAGAGAGGACACAGGCGCGCTGGCTGCCGGAGGAGAAAGGAGAGA GCCCCTCCCCTACCCCTTCCTAGAGAGGACACGGGCGCGCTGGCTGCCGGAGGAGAAAGGAGAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:35119675..35119808 26863196 MeRIP-seq:(Medium) rs1285772390 Functional Loss SNV dbSNP153 33..33 33 - - - 108478 RMVar_ID_108478 Human_SNP_ID_622810731 m1A Human chr17 - 35137619 35137619 35137619 CTGTCCTTCAGATTCTCCTCTGGGACCCAAGCACAGGGAAGCAGGTGGGCAGGACCCTCGCTGGC CTGTCCTTCAGATTCTCCTCTGGGACCCAAGCCCAGGGAAGCAGGTGGGCAGGACCCTCGCTGGC T G NLE1 Ensembl:ENSG00000073536 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:35137038..35137636 32194978 MeRIP-seq:(Medium) rs1374612864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899786,Human_RBP_ID_4471100,Human_RBP_ID_25272794 Human_Splice_Rec_1804732,Human_Splice_Rec_1804733,Human_Splice_Rec_1804754,Human_Splice_Rec_1804755,Human_Splice_Rec_1804776,Human_Splice_Rec_1804777,Human_Splice_Rec_1804814,Human_Splice_Rec_1804815,Human_Splice_Rec_1804834,Human_Splice_Rec_1804835 RMVar_hsa_circ_116810,RMVar_hsa_circ_183635,RMVar_hsa_circ_127878,RMVar_hsa_circ_85380,RMVar_hsa_circ_183638,RMVar_hsa_circ_370290,RMVar_hsa_circ_183639,RMVar_hsa_circ_267634,RMVar_hsa_circ_183641,RMVar_hsa_circ_80607,RMVar_hsa_circ_183643,RMVar_hsa_circ_76941,RMVar_hsa_circ_377452,RMVar_hsa_circ_11509,RMVar_hsa_circ_183644,RMVar_hsa_circ_183646,RMVar_hsa_circ_85535,RMVar_hsa_circ_115376,RMVar_hsa_circ_183647 108479 RMVar_ID_108479 Human_SNP_ID_622811950 m1A Human chr17 - 35142103 35142103 35142103 CTTGCTCGCGCAGGACGAGGCGGTGGCGCGCGATGTGCAGCGGTTGCTAGTGCAGTTCCAGGATG CTTGCTCGCGCAGGACGAGGCGGTGGCGCGCGTTGTGCAGCGGTTGCTAGTGCAGTTCCAGGATG T A NLE1 Ensembl:ENSG00000073536 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:35142052..35142251 26863196 MeRIP-seq:(Medium) rs181807693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_897503,Human_RBP_ID_4465294,Human_RBP_ID_5364033 Human_Splice_Rec_1804724,Human_Splice_Rec_1804770,Human_Splice_Rec_1804806,Human_Splice_Rec_1804828 RMVar_hsa_circ_377452 108480 RMVar_ID_108480 Human_SNP_ID_622814412 m1A Human chr17 - 35151197 35151197 35151197 CGCTGAATTTAAGCATATTTGTCAGCGGAGGAAAAGAAACTAACCAGGATTCCCTCAGTAATGGC CGCTGAATTTAAGCATATTTGTCAGCGGAGGAGAAGAAACTAACCAGGATTCCCTCAGTAATGGC T C RF02543-021 RNACentral:URS000096B15F rRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12165042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269916,Human_RBP_ID_278128,Human_RBP_ID_487350,Human_RBP_ID_1007430,Human_RBP_ID_1090396,Human_RBP_ID_1181304,Human_RBP_ID_1285759,Human_RBP_ID_1531696,Human_RBP_ID_1855201,Human_RBP_ID_2529294,Human_RBP_ID_3519891,Human_RBP_ID_4419742,Human_RBP_ID_5184461,Human_RBP_ID_5260019,Human_RBP_ID_5275057,Human_RBP_ID_5419990,Human_RBP_ID_5441319,Human_RBP_ID_5466348,Human_RBP_ID_5496861,Human_RBP_ID_5577099,Human_RBP_ID_6584338,Human_RBP_ID_8089712,Human_RBP_ID_8253331,Human_RBP_ID_8449720,Human_RBP_ID_8816443,Human_RBP_ID_9071295,Human_RBP_ID_9257367,Human_RBP_ID_9287242,Human_RBP_ID_9856137,Human_RBP_ID_10483399,Human_RBP_ID_12970319,Human_RBP_ID_17004291,Human_RBP_ID_17063127,Human_RBP_ID_17067912,Human_RBP_ID_17126327,Human_RBP_ID_17190236,Human_RBP_ID_17259153,Human_RBP_ID_17375087,Human_RBP_ID_17490472,Human_RBP_ID_17691782,Human_RBP_ID_17889966,Human_RBP_ID_18179320,Human_RBP_ID_18200129,Human_RBP_ID_18207783,Human_RBP_ID_18291248,Human_RBP_ID_18438752,Human_RBP_ID_18513587,Human_RBP_ID_18530577,Human_RBP_ID_18694818,Human_RBP_ID_20203111,Human_RBP_ID_21889613,Human_RBP_ID_21926904,Human_RBP_ID_22212300,Human_RBP_ID_22422060,Human_RBP_ID_22499210,Human_RBP_ID_22804032,Human_RBP_ID_22949715,Human_RBP_ID_23129097,Human_RBP_ID_23168616,Human_RBP_ID_23275469,Human_RBP_ID_23308812,Human_RBP_ID_23721702,Human_RBP_ID_24478586,Human_RBP_ID_24531813,Human_RBP_ID_25272825,Human_RBP_ID_26449272,Human_RBP_ID_26641589,Human_RBP_ID_26749069,Human_RBP_ID_26959008,Human_RBP_ID_27156494,Human_RBP_ID_27252697,Human_RBP_ID_27451054,Human_RBP_ID_27560927,Human_RBP_ID_27664074 108481 RMVar_ID_108481 Human_SNP_ID_622814462 m1A Human chr17 - 35151325 35151325 35151325 TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGAAATGTGGCGTACGGAAGACCCACTCCCCGGCGC TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGACATGTGGCGTACGGAAGACCCACTCCCCGGCGC T G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62062411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269922,Human_RBP_ID_1091851,Human_RBP_ID_4471122,Human_RBP_ID_5189099,Human_RBP_ID_5274904,Human_RBP_ID_5577105,Human_RBP_ID_6662142,Human_RBP_ID_8093684,Human_RBP_ID_8816448,Human_RBP_ID_9078515,Human_RBP_ID_9856148,Human_RBP_ID_10483404,Human_RBP_ID_12970340,Human_RBP_ID_17063131,Human_RBP_ID_17190239,Human_RBP_ID_17259158,Human_RBP_ID_17691787,Human_RBP_ID_17889976,Human_RBP_ID_18179330,Human_RBP_ID_18200138,Human_RBP_ID_18207789,Human_RBP_ID_22212303,Human_RBP_ID_22390159,Human_RBP_ID_22960547,Human_RBP_ID_23275477,Human_RBP_ID_23308819,Human_RBP_ID_23721728,Human_RBP_ID_24415132,Human_RBP_ID_24478587,Human_RBP_ID_25272833,Human_RBP_ID_26449279,Human_RBP_ID_27156502,Human_RBP_ID_27451062 108482 RMVar_ID_108482 Human_SNP_ID_622865961 m1A Human chr17 - 35352619 35352619 35352619 ATTCTCCAAAGGATGTTGCTGTGCTTGTCAGCACCGCAAAAGAAGTGGAGCACTATAAGTATGAG ATTCTCCAAAGGATGTTGCTGTGCTTGTCAGCGCCGCAAAAGAAGTGGAGCACTATAAGTATGAG T C SLFN11 Ensembl:ENSG00000172716 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:35352386..35353033 32194978 MeRIP-seq:(Medium) rs1322820152 Functional Loss SNV dbSNP153 33..33 33 - - - 108483 RMVar_ID_108483 Human_SNP_ID_622927115 m1A Human chr17 - 35587377 35587377 35587377 GAGGGCGGGGGTGGCGGCGGGAGCCGGAGAGCACAGCCCAGGTGGTGGTGTAATGGTTTCCTGCC GAGGGCGGGGGTGGCGGCGGGAGCCGGAGAGCGCAGCCCAGGTGGTGGTGTAATGGTTTCCTGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr17:35587326..35587551;chr17:35587326..35587520;chr17:35587326..35587618;chr17:35587326..35587600 26863196 MeRIP-seq:(Medium) rs998762618 Functional Loss SNV dbSNP153 33..33 33 - - - 108484 RMVar_ID_108484 Human_SNP_ID_622927132 m1A Human chr17 - 35587419 35587414 35587420 AAAGGCAACCGCCCTGAACTCACCGGAGGCGGAGGCGAAGGCGAGGGCGGGGGTGGCGGCGGGAG AAAGGCAACCGCCCTGAACTCACCGGAGGCG______AAGGCGAGGGCGGGGGTGGCGGCGGGAG TCGCCTC T - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:35587351..35587450 26863410 MeRIP-seq:(Medium) rs1241452640 Functional Loss DEL dbSNP153 32..37 33 - - - 108485 RMVar_ID_108485 Human_SNP_ID_622927139 m1A Human chr17 - 35587425 35587425 35587425 CACCCTAAAGGCAACCGCCCTGAACTCACCGGAGGCGGAGGCGAAGGCGAGGGCGGGGGTGGCGG CACCCTAAAGGCAACCGCCCTGAACTCACCGGGGGCGGAGGCGAAGGCGAGGGCGGGGGTGGCGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:35587327..35587606 26863196 MeRIP-seq:(Medium) rs1439055058 Functional Loss SNV dbSNP153 33..33 33 - - - 108486 RMVar_ID_108486 Human_SNP_ID_622928580 m1A Human chr17 + 35593943 35593939 35593944 AAGTGTTCCTAAAATTAATTGGATGTTCTTAAAATTAATTGGATGCCTTGTTGGATATCTATAAC AAGTGTTCCTAAAATTAATTGGATGTTCT_____TTAATTGGATGCCTTGTTGGATATCTATAAC TTAAAA T AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:35593940..35594054 26863196 MeRIP-seq:(Medium) rs769636002 Functional Loss DEL dbSNP153 30..34 33 - - - 108487 RMVar_ID_108487 Human_SNP_ID_622928599 m1A Human chr17 + 35594006 35594006 35594006 ACCTGAATGAAGGAATTCTTTTCTCTTGCTATAGGTGCACATTAAAGATCCAAAGTCATGACTGA ACCTGAATGAAGGAATTCTTTTCTCTTGCTATGGGTGCACATTAAAGATCCAAAGTCATGACTGA A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr17:35594001..35594025;chr17:35594001..35594075 26863196 MeRIP-seq:(Medium) rs747168542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1805301,Human_Splice_Rec_1805309,Human_Splice_Rec_1805333,Human_Splice_Rec_1805371,Human_Splice_Rec_1805397,Human_Splice_Rec_1805437,Human_Splice_Rec_1805477,Human_Splice_Rec_1805487,Human_Splice_Rec_1805495,Human_Splice_Rec_1805521,Human_Splice_Rec_1805561,Human_Splice_Rec_1805589,Human_Splice_Rec_1805595,Human_Splice_Rec_1805635,Human_Splice_Rec_1805675,Human_Splice_Rec_1805681,Human_Splice_Rec_1805689,Human_Splice_Rec_1805695 RMVar_hsa_circ_311341,RMVar_hsa_circ_373424 108488 RMVar_ID_108488 Human_SNP_ID_622943061 m1A Human chr17 - 35654961 35654961 35654961 AACTCGGCAAATCTTACCCAGCTTGTTTACCAAAAACATCACCGCTAGCATTACCAGTAGTAGAG AACTCGGCAAATCTTACCCAGCTTGTTTACCAGAAACATCACCGCTAGCATTACCAGTAGTAGAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:35654876..35655043;chr17:35654862..35655045 26863196 MeRIP-seq:(Medium) rs1030913303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17189456 108489 RMVar_ID_108489 Human_SNP_ID_622959471 m1A Human chr17 + 35725842 35725842 35725842 TTTCCTATCAGAATATGTCCCTCAACCCCCGAAACAAGGCTTCTCTCAGCCTCCCCACCAGTGAT TTTCCTATCAGAATATGTCCCTCAACCCCCGAGACAAGGCTTCTCTCAGCCTCCCCACCAGTGAT A G TAF15,AP2B1 Ensembl:ENSG00000270647,Ensembl:ENSG00000006125 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:35725776..35725875 26863196 MeRIP-seq:(Medium) rs1320075210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5115110,Human_RBP_ID_17378281,Human_RBP_ID_18190781,Human_RBP_ID_22587945,Human_RBP_ID_26449443 108490 RMVar_ID_108490 Human_SNP_ID_622960970 m1A Human chr17 - 35731880 35731880 35731880 ACCCCTGACCGCTTCCCCTCCTCCCGCCGCTTACCCGGGGCCGTCCTAGCTGCCCCCTGCCCTGG ACCCCTGACCGCTTCCCCTCCTCCCGCCGCTTCCCCGGGGCCGTCCTAGCTGCCCCCTGCCCTGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:35731840..35731930 26863196 MeRIP-seq:(Medium) rs1555596422 Functional Loss SNV dbSNP153 33..33 33 - - - 108491 RMVar_ID_108491 Human_SNP_ID_622980890 m1A Human chr17 - 35809542 35809542 35809542 GACATGACTAACGGCCGCGGCGCGGAGGCCCCACAGCCCGCCGAGAACAACGAATACGAAAGCCA GACATGACTAACGGCCGCGGCGCGGAGGCCCCGCAGCCCGCCGAGAACAACGAATACGAAAGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:35713790..35809747;chr17:35809476..35809763 26863196 MeRIP-seq:(Medium) rs1483275097 Functional Loss SNV dbSNP153 33..33 33 - - - 108492 RMVar_ID_108492 Human_SNP_ID_622980908 m1A Human chr17 - 35809578 35809578 35809578 GTCGCTGCCGCTGCTCGCTGAAGAAGTCACCTACCCGACATGACTAACGGCCGCGGCGCGGAGGC GTCGCTGCCGCTGCTCGCTGAAGAAGTCACCTTCCCGACATGACTAACGGCCGCGGCGCGGAGGC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:35809547..35809716 32194978 MeRIP-seq:(Medium) rs1568235080 Functional Loss SNV dbSNP153 33..33 33 - - - 108493 RMVar_ID_108493 Human_SNP_ID_622981021 m1A Human chr17 + 35809846 35809846 35809846 TGGAACCCGAGGAGACTTGCCGTTCCCGGGGGAGGGTGTGTGTGAGTCGGGGGGCGGAGGCCGTC TGGAACCCGAGGAGACTTGCCGTTCCCGGGGGGGGGTGTGTGTGAGTCGGGGGGCGGAGGCCGTC A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:35809843..35810045;chr17:35809840..35809997 26863196 MeRIP-seq:(Medium) rs1214195682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1066579,Human_RBP_ID_5366737,Human_RBP_ID_6585287,Human_RBP_ID_22063091 RMVar_hsa_circ_88237,RMVar_hsa_circ_183687 108494 RMVar_ID_108494 Human_SNP_ID_622983414 m1A Human chr17 + 35817753 35817753 35817753 GGAAGTTACGGTCAGTCTGGGGGTGAGCAGCAAAGGTAAAGTATACATACATTTTAATAATATGA GGAAGTTACGGTCAGTCTGGGGGTGAGCAGCAGAGGTAAAGTATACATACATTTTAATAATATGA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:35817664..35817810;chr17:35817701..35817775 26863196 MeRIP-seq:(Medium) rs773808943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1531903,Human_RBP_ID_4465304,Human_RBP_ID_6585444,Human_RBP_ID_12972578,Human_RBP_ID_19082173 Human_Splice_Rec_1805744,Human_Splice_Rec_1805745,Human_Splice_Rec_1805764,Human_Splice_Rec_1805765,Human_Splice_Rec_1805774,Human_Splice_Rec_1805775,Human_Splice_Rec_1805782,Human_Splice_Rec_1805783,Human_Splice_Rec_1805790,Human_Splice_Rec_1805791,Human_Splice_Rec_1805818,Human_Splice_Rec_1805819,Human_Splice_Rec_1805850,Human_Splice_Rec_1805851,Human_Splice_Rec_1805880,Human_Splice_Rec_1805881,Human_Splice_Rec_1805910,Human_Splice_Rec_1805911 RMVar_hsa_circ_34113,RMVar_hsa_circ_88237,RMVar_hsa_circ_66590,RMVar_hsa_circ_348996,RMVar_hsa_circ_183687,RMVar_hsa_circ_295543,RMVar_hsa_circ_347362,RMVar_hsa_circ_183688,RMVar_hsa_circ_326340 108495 RMVar_ID_108495 Human_SNP_ID_622983997 m1A Human chr17 - 35820003 35820003 35820003 TAGGTAGAATAACTGCAAAAGAAAAATTTAATACTTGAAAGAAATGTGTAGAAATTTTAAAGTTT TAGGTAGAATAACTGCAAAAGAAAAATTTAATGCTTGAAAGAAATGTGTAGAAATTTTAAAGTTT T C AC015849.3 Ensembl:ENSG00000270871 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:35820001..35820075;chr17:35820001..35820250;chr17:35820001..35820252 26863196 MeRIP-seq:(Medium) rs753596990 Functional Loss SNV dbSNP153 33..33 33 - - - 108496 RMVar_ID_108496 Human_SNP_ID_622983998 m1A Human chr17 + 35820004 35820004 35820004 AACTTTAAAATTTCTACACATTTCTTTCAAGTATTAAATTTTTCTTTTGCAGTTATTCTACCTAT AACTTTAAAATTTCTACACATTTCTTTCAAGTGTTAAATTTTTCTTTTGCAGTTATTCTACCTAT A G TAF15,AC015849.4 Ensembl:ENSG00000270647,Ensembl:ENSG00000270894 Protein coding,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:35820001..35820075 26863196 MeRIP-seq:(Medium) rs754559084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3520283,Human_RBP_ID_12972721,Human_RBP_ID_22004275,Human_RBP_ID_22656143,Human_RBP_ID_25273732 Human_Splice_Rec_1805747,Human_Splice_Rec_1805767,Human_Splice_Rec_1805777,Human_Splice_Rec_1805793,Human_Splice_Rec_1805821,Human_Splice_Rec_1805853,Human_Splice_Rec_1805883,Human_Splice_Rec_1805913 RMVar_hsa_circ_34113,RMVar_hsa_circ_88237,RMVar_hsa_circ_348996,RMVar_hsa_circ_183687,RMVar_hsa_circ_295543,RMVar_hsa_circ_347362,RMVar_hsa_circ_183688,RMVar_hsa_circ_326340 108497 RMVar_ID_108497 Human_SNP_ID_622984023 m1A Human chr17 - 35820098 35820098 35820098 CTACTTAAGATAAAAATAACTACTTATGAAGAATACAATTTATATTTCAACCTACTTGTGATGCT CTACTTAAGATAAAAATAACTACTTATGAAGAGTACAATTTATATTTCAACCTACTTGTGATGCT T C AC015849.3 Ensembl:ENSG00000270871 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:35820096..35820189 26863196 MeRIP-seq:(Medium) rs559861539 Functional Loss SNV dbSNP153 33..33 33 - - - 108498 RMVar_ID_108498 Human_SNP_ID_622989320 m1A Human chr17 - 35838528 35838528 35838528 GGCATACCATCAAACCAGTCAATGGCTGCCTTAGCTGAAGGAGGGTCATCAAATGACACTGTTGC GGCATACCATCAAACCAGTCAATGGCTGCCTTGGCTGAAGGAGGGTCATCAAATGACACTGTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:35838378..35838596 26863196 MeRIP-seq:(Medium) rs1291002866 Functional Loss SNV dbSNP153 33..33 33 - - - 108499 RMVar_ID_108499 Human_SNP_ID_622991175 m1A Human chr17 + 35844563 35844563 35844563 GAGGTGGAGACCGAGGCGGCTATGGTGGAGACAGAAGTGGGGGTGGCTATGGTGGAGACAGAAGC GAGGTGGAGACCGAGGCGGCTATGGTGGAGACGGAAGTGGGGGTGGCTATGGTGGAGACAGAAGC A G TAF15 Ensembl:ENSG00000270647 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:35844551..35844575 26863196 MeRIP-seq:(Medium) rs753239090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952171,Human_RBP_ID_4420549,Human_RBP_ID_8189571,Human_RBP_ID_8232168,Human_RBP_ID_9346237,Human_RBP_ID_9422831,Human_RBP_ID_10483406,Human_RBP_ID_17653799,Human_RBP_ID_18941587,Human_RBP_ID_22421869,Human_RBP_ID_23276435,Human_RBP_ID_26331595 Human_Splice_Rec_1805844,Human_Splice_Rec_1805845,Human_Splice_Rec_1805876,Human_Splice_Rec_1805906,Human_Splice_Rec_1805932 108500 RMVar_ID_108500 Human_SNP_ID_622991299 m1A Human chr17 - 35844730 35844682 35844730 CCTCCATAGCCACCTCGATCTCCTCCATAGCCACCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT CCTCCATAGCCACCTCGATCTCCTCCATAGCC_________________________________ CGGCTATGGTGGGGACAGAGGAGGCGGCTATGGAGGAGACCGAGGAGGT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:35844515..35845012 26863410 MeRIP-seq:(Medium) rs765994777 Functional Loss DEL dbSNP153 33..65 33 - - - 108501 RMVar_ID_108501 Human_SNP_ID_622991330 m1A Human chr17 - 35844730 35844706 35844730 CCTCCATAGCCACCTCGATCTCCTCCATAGCCACCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT CCTCCATAGCCACCTCGATCTCCTCCATAGCC________________________GCCTCCTCT CGGCTATGGAGGAGACCGAGGAGGT C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:35844515..35845012 26863410 MeRIP-seq:(Medium) rs779199064 Functional Loss DEL dbSNP153 33..56 33 - - - 108502 RMVar_ID_108502 Human_SNP_ID_622991353 m1A Human chr17 - 35844730 35844730 35844730 CCTCCATAGCCACCTCGATCTCCTCCATAGCCACCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT CCTCCATAGCCACCTCGATCTCCTCCATAGCCTCCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:35844515..35845012 26863410 MeRIP-seq:(Medium) rs144917137 Functional Loss SNV dbSNP153 33..33 33 - - - 108503 RMVar_ID_108503 Human_SNP_ID_622991354 m1A Human chr17 - 35844730 35844730 35844730 CCTCCATAGCCACCTCGATCTCCTCCATAGCCACCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT CCTCCATAGCCACCTCGATCTCCTCCATAGCCGCCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:35844515..35845012 26863410 MeRIP-seq:(Medium) rs144917137 Functional Loss SNV dbSNP153 33..33 33 - - - 108504 RMVar_ID_108504 Human_SNP_ID_622991355 m1A Human chr17 - 35844730 35844730 35844730 CCTCCATAGCCACCTCGATCTCCTCCATAGCCACCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT CCTCCATAGCCACCTCGATCTCCTCCATAGCCCCCTCCTCGGTCTCCTCCATAGCCGCCTCCTCT T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:35844515..35845012 26863410 MeRIP-seq:(Medium) rs144917137 Functional Loss SNV dbSNP153 33..33 33 - - - 108505 RMVar_ID_108505 Human_SNP_ID_622991401 m1A Human chr17 - 35844772 35844772 35844772 CCATAGCCTCCTCGGTCTCCACCATAGCCTCCACCTCGGTCTCCTCCATAGCCACCTCGATCTCC CCATAGCCTCCTCGGTCTCCACCATAGCCTCCTCCTCGGTCTCCTCCATAGCCACCTCGATCTCC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEK293T,Starvation treatment chr17:35844257..35845050;chr17:35844540..35844851 26863196,26863410 MeRIP-seq:(Medium) rs745378926 Functional Loss SNV dbSNP153 33..33 33 - - - 108506 RMVar_ID_108506 Human_SNP_ID_622991538 m1A Human chr17 + 35844945 35844945 35844945 CAGTGGCTACGGTGGAGACCGAAGTGGAGGCTATGGAGGAGACAGGAGTGGTGGCGGCTATGGAG CAGTGGCTACGGTGGAGACCGAAGTGGAGGCTCTGGAGGAGACAGGAGTGGTGGCGGCTATGGAG A C TAF15 Ensembl:ENSG00000270647 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:35844597..35845025 26863196 MeRIP-seq:(Medium) rs202014042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6774,Human_RBP_ID_51048,Human_RBP_ID_238389,Human_RBP_ID_5115435,Human_RBP_ID_5143165,Human_RBP_ID_6585977,Human_RBP_ID_8816641,Human_RBP_ID_8941893,Human_RBP_ID_9257814,Human_RBP_ID_9423967,Human_RBP_ID_12973906,Human_RBP_ID_17653802,Human_RBP_ID_18164188,Human_RBP_ID_18438775,Human_RBP_ID_22421871,Human_RBP_ID_23118751,Human_RBP_ID_25274338,Human_RBP_ID_26331598,Human_RBP_ID_26458954,Human_RBP_ID_27813720 Human_Splice_Rec_1805846,Human_Splice_Rec_1805847,Human_Splice_Rec_1805877,Human_Splice_Rec_1805907,Human_Splice_Rec_1805934,Human_Splice_Rec_1805935,Human_Splice_Rec_1805937 108507 RMVar_ID_108507 Human_SNP_ID_622991539 m1A Human chr17 + 35844945 35844945 35844945 CAGTGGCTACGGTGGAGACCGAAGTGGAGGCTATGGAGGAGACAGGAGTGGTGGCGGCTATGGAG CAGTGGCTACGGTGGAGACCGAAGTGGAGGCTGTGGAGGAGACAGGAGTGGTGGCGGCTATGGAG A G TAF15 Ensembl:ENSG00000270647 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:35844597..35845025 26863196 MeRIP-seq:(Medium) rs202014042 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_6774,Human_RBP_ID_51048,Human_RBP_ID_238389,Human_RBP_ID_5115435,Human_RBP_ID_5143165,Human_RBP_ID_6585977,Human_RBP_ID_8816641,Human_RBP_ID_8941893,Human_RBP_ID_9257814,Human_RBP_ID_9423967,Human_RBP_ID_12973906,Human_RBP_ID_17653802,Human_RBP_ID_18164188,Human_RBP_ID_18438775,Human_RBP_ID_22421871,Human_RBP_ID_23118751,Human_RBP_ID_25274338,Human_RBP_ID_26331598,Human_RBP_ID_26458954,Human_RBP_ID_27813720 Human_Splice_Rec_1805846,Human_Splice_Rec_1805847,Human_Splice_Rec_1805877,Human_Splice_Rec_1805907,Human_Splice_Rec_1805934,Human_Splice_Rec_1805935,Human_Splice_Rec_1805937 108508 RMVar_ID_108508 Human_SNP_ID_622991591 m1A Human chr17 + 35845025 35845025 35845025 GCTACGGAGGAGACCGAGGTGGCTATGGAGGCAAAATGGGAGGAAGGTGAGTATTAGAATGTGTT GCTACGGAGGAGACCGAGGTGGCTATGGAGGCCAAATGGGAGGAAGGTGAGTATTAGAATGTGTT A C TAF15 Ensembl:ENSG00000270647 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:35844763..35846929 32194978 MeRIP-seq:(Medium) rs769805184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6775,Human_RBP_ID_1855644,Human_RBP_ID_3547392,Human_RBP_ID_3950404,Human_RBP_ID_5115435,Human_RBP_ID_5143510,Human_RBP_ID_6585980,Human_RBP_ID_8232170,Human_RBP_ID_9375711,Human_RBP_ID_9423967,Human_RBP_ID_18164673,Human_RBP_ID_21890053,Human_RBP_ID_22475073,Human_RBP_ID_22587952,Human_RBP_ID_23114406,Human_RBP_ID_23118752,Human_RBP_ID_23275538,Human_RBP_ID_23722107,Human_RBP_ID_26331599,Human_RBP_ID_27812562 Human_Splice_Rec_1805847,Human_Splice_Rec_1805877,Human_Splice_Rec_1805907,Human_Splice_Rec_1805935,Human_Splice_Rec_1805937 108509 RMVar_ID_108509 Human_SNP_ID_622991592 m1A Human chr17 + 35845025 35845025 35845025 GCTACGGAGGAGACCGAGGTGGCTATGGAGGCAAAATGGGAGGAAGGTGAGTATTAGAATGTGTT GCTACGGAGGAGACCGAGGTGGCTATGGAGGCGAAATGGGAGGAAGGTGAGTATTAGAATGTGTT A G TAF15 Ensembl:ENSG00000270647 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:35844763..35846929 32194978 MeRIP-seq:(Medium) rs769805184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6775,Human_RBP_ID_1855644,Human_RBP_ID_3547392,Human_RBP_ID_3950404,Human_RBP_ID_5115435,Human_RBP_ID_5143510,Human_RBP_ID_6585980,Human_RBP_ID_8232170,Human_RBP_ID_9375711,Human_RBP_ID_9423967,Human_RBP_ID_18164673,Human_RBP_ID_21890053,Human_RBP_ID_22475073,Human_RBP_ID_22587952,Human_RBP_ID_23114406,Human_RBP_ID_23118752,Human_RBP_ID_23275538,Human_RBP_ID_23722107,Human_RBP_ID_26331599,Human_RBP_ID_27812562 Human_Splice_Rec_1805847,Human_Splice_Rec_1805877,Human_Splice_Rec_1805907,Human_Splice_Rec_1805935,Human_Splice_Rec_1805937 108510 RMVar_ID_108510 Human_SNP_ID_623135725 m1A Human chr17 - 36486725 36486725 36486725 ATTTGGGCTTCTCCAAGCAGATCACGCAGACGACGGTGCTACATTTGAGCGACGCCATGGTTTTG ATTTGGGCTTCTCCAAGCAGATCACGCAGACGGCGGTGCTACATTTGAGCGACGCCATGGTTTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:36486676..36486908 26863196 MeRIP-seq:(Medium) rs1222470225 Functional Loss SNV dbSNP153 33..33 33 - - - 108511 RMVar_ID_108511 Human_SNP_ID_623135740 m1A Human chr17 - 36486742 36486742 36486742 GCAGGCTGGACAGCGGTATTTGGGCTTCTCCAAGCAGATCACGCAGACGACGGTGCTACATTTGA GCAGGCTGGACAGCGGTATTTGGGCTTCTCCAGGCAGATCACGCAGACGACGGTGCTACATTTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36486676..36486836 26863196 MeRIP-seq:(Medium) rs1403934002 Functional Loss SNV dbSNP153 33..33 33 - - - 108512 RMVar_ID_108512 Human_SNP_ID_623135750 m1A Human chr17 + 36486758 36486758 36486758 CGTCTGCGTGATCTGCTTGGAGAAGCCCAAATACCGCTGTCCAGCCTGCCGCGTGCCCTAGTGAG CGTCTGCGTGATCTGCTTGGAGAAGCCCAAATGCCGCTGTCCAGCCTGCCGCGTGCCCTAGTGAG A G ZNHIT3 Ensembl:ENSG00000273611 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:36486708..36486858 26863196 MeRIP-seq:(Medium) rs760298652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420621,Human_RBP_ID_22445399,Human_RBP_ID_26812152,Human_RBP_ID_27451154 Human_Splice_Rec_1806813,Human_Splice_Rec_1806819,Human_Splice_Rec_1806825,Human_Splice_Rec_1806827,Human_Splice_Rec_1806835,Human_Splice_Rec_1806841,Human_Splice_Rec_1806849,Human_Splice_Rec_1806857,Human_Splice_Rec_1806859 RMVar_hsa_circ_68398 108513 RMVar_ID_108513 Human_SNP_ID_623135751 m1A Human chr17 + 36486758 36486758 36486758 CGTCTGCGTGATCTGCTTGGAGAAGCCCAAATACCGCTGTCCAGCCTGCCGCGTGCCCTAGTGAG CGTCTGCGTGATCTGCTTGGAGAAGCCCAAATTCCGCTGTCCAGCCTGCCGCGTGCCCTAGTGAG A T ZNHIT3 Ensembl:ENSG00000273611 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:36486708..36486858 26863196 MeRIP-seq:(Medium) rs760298652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420621,Human_RBP_ID_22445399,Human_RBP_ID_26812152,Human_RBP_ID_27451154 Human_Splice_Rec_1806813,Human_Splice_Rec_1806819,Human_Splice_Rec_1806825,Human_Splice_Rec_1806827,Human_Splice_Rec_1806835,Human_Splice_Rec_1806841,Human_Splice_Rec_1806849,Human_Splice_Rec_1806857,Human_Splice_Rec_1806859 RMVar_hsa_circ_68398 108514 RMVar_ID_108514 Human_SNP_ID_623137634 m1A Human chr17 + 36492851 36492849 36492852 GCAACCCTGAAACTCGTCCTGTTGAGAAAAAAATAAGATCAGCTCTTCCTACCAAAACCGTAAAG GCAACCCTGAAACTCGTCCTGTTGAGAAAAA___AAGATCAGCTCTTCCTACCAAAACCGTAAAG AAAT A ZNHIT3 Ensembl:ENSG00000273611 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36492755..36492850 26863196 MeRIP-seq:(Medium) rs1334192909 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1007536,Human_RBP_ID_1855694,Human_RBP_ID_3520542 Human_Splice_Rec_1806814,Human_Splice_Rec_1806815,Human_Splice_Rec_1806820,Human_Splice_Rec_1806821,Human_Splice_Rec_1806826,Human_Splice_Rec_1806830,Human_Splice_Rec_1806831,Human_Splice_Rec_1806836,Human_Splice_Rec_1806837,Human_Splice_Rec_1806844,Human_Splice_Rec_1806845,Human_Splice_Rec_1806852,Human_Splice_Rec_1806853,Human_Splice_Rec_1806863,Human_Splice_Rec_1806868,Human_Splice_Rec_1806869,Human_Splice_Rec_1806874,Human_Splice_Rec_1806875 RMVar_hsa_circ_112000,RMVar_hsa_circ_68398,RMVar_hsa_circ_365038,RMVar_hsa_circ_13562,RMVar_hsa_circ_183703,RMVar_hsa_circ_183704 108515 RMVar_ID_108515 Human_SNP_ID_623137635 m1A Human chr17 + 36492851 36492850 36492852 GCAACCCTGAAACTCGTCCTGTTGAGAAAAAAATAAGATCAGCTCTTCCTACCAAAACCGTAAAG GCAACCCTGAAACTCGTCCTGTTGAGAAAAAA__AAGATCAGCTCTTCCTACCAAAACCGTAAAG AAT A ZNHIT3 Ensembl:ENSG00000273611 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36492755..36492850 26863196 MeRIP-seq:(Medium) rs1567716150 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1007536,Human_RBP_ID_1855694,Human_RBP_ID_3520542 Human_Splice_Rec_1806814,Human_Splice_Rec_1806815,Human_Splice_Rec_1806820,Human_Splice_Rec_1806821,Human_Splice_Rec_1806826,Human_Splice_Rec_1806830,Human_Splice_Rec_1806831,Human_Splice_Rec_1806836,Human_Splice_Rec_1806837,Human_Splice_Rec_1806844,Human_Splice_Rec_1806845,Human_Splice_Rec_1806852,Human_Splice_Rec_1806853,Human_Splice_Rec_1806863,Human_Splice_Rec_1806868,Human_Splice_Rec_1806869,Human_Splice_Rec_1806874,Human_Splice_Rec_1806875 RMVar_hsa_circ_112000,RMVar_hsa_circ_68398,RMVar_hsa_circ_365038,RMVar_hsa_circ_13562,RMVar_hsa_circ_183703,RMVar_hsa_circ_183704 108516 RMVar_ID_108516 Human_SNP_ID_623138697 m1A Human chr17 + 36496247 36496247 36496247 CAGGAAAAGGCCTTGTGGAAACAAAGGCACCAAGGATCACCCCAGCCCAGTGAAGGCAGAAGAGG CAGGAAAAGGCCTTGTGGAAACAAAGGCACCAGGGATCACCCCAGCCCAGTGAAGGCAGAAGAGG A G ZNHIT3 Ensembl:ENSG00000273611 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36496196..36496270 26863196 MeRIP-seq:(Medium) rs368506948 Functional Loss SNV dbSNP153 33..33 33 - - - 108517 RMVar_ID_108517 Human_SNP_ID_623141997 m1A Human chr17 + 36507013 36507013 36507013 GCCTGCTGTGTGGTACCGCACAGGCCCCGCATAATGCACCACAATGAAGCTGGGCTCCCGGCTGA GCCTGCTGTGTGGTACCGCACAGGCCCCGCATGATGCACCACAATGAAGCTGGGCTCCCGGCTGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36506790..36507047 32194978 MeRIP-seq:(Medium) rs1451963318 Functional Loss SNV dbSNP153 33..33 33 - - - 108518 RMVar_ID_108518 Human_SNP_ID_623142337 m1A Human chr17 + 36507890 36507890 36507890 TAGTTGATGCACAACTGTTCCAGACTGTTGTCAGGAAATGATTCAAATCCATACACATCCAGCAG TAGTTGATGCACAACTGTTCCAGACTGTTGTCTGGAAATGATTCAAATCCATACACATCCAGCAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36507405..36507890 32194978 MeRIP-seq:(Medium) rs1279724905 Functional Loss SNV dbSNP153 33..33 33 - - - 108519 RMVar_ID_108519 Human_SNP_ID_623143961 m1A Human chr17 - 36513220 36513220 36513220 TGGGGTGGACGGGGCATAAGGAAGAGTGATGCATACACAGTGCTAGAGTACAGAATGCAGTAAGT TGGGGTGGACGGGGCATAAGGAAGAGTGATGCGTACACAGTGCTAGAGTACAGAATGCAGTAAGT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36513214..36513297 32194978 MeRIP-seq:(Medium) rs1405103190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49898,Human_RBP_ID_5366750,Human_RBP_ID_12976661,Human_RBP_ID_19085131,Human_RBP_ID_22950215 RMVar_hsa_circ_337596,RMVar_hsa_circ_339259 108520 RMVar_ID_108520 Human_SNP_ID_623143987 m1A Human chr17 + 36513307 36513307 36513307 AGAACAGAGGTGACTGATTCCTTGGAGGTAGCACAGAAGGGCCCAAAGTCCTAGATCCTCAGGGA AGAACAGAGGTGACTGATTCCTTGGAGGTAGCCCAGAAGGGCCCAAAGTCCTAGATCCTCAGGGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36513302..36513402 32194978 MeRIP-seq:(Medium) rs6607296 Functional Loss SNV dbSNP153 33..33 33 - - - 108521 RMVar_ID_108521 Human_SNP_ID_623147929 m1A Human chr17 - 36526355 36526355 36526355 AGGAGGGAGGTCTTGGGGGCAAGAGGGAGTAGATGAGAGCAGGAAGACGAGAAAGCCAGGGTTGT AGGAGGGAGGTCTTGGGGGCAAGAGGGAGTAGGTGAGAGCAGGAAGACGAGAAAGCCAGGGTTGT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:36526153..36526514 26863196 MeRIP-seq:(Medium) rs12602787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820854,Human_RBP_ID_6586888,Human_RBP_ID_12977218,Human_RBP_ID_23276438,Human_RBP_ID_25274802 RMVar_hsa_circ_337596,RMVar_hsa_circ_183716,RMVar_hsa_circ_272953 108522 RMVar_ID_108522 Human_SNP_ID_623147933 m1A Human chr17 + 36526377 36526377 36526377 CCTGCTCTCATCTACTCCCTCTTGCCCCCAAGACCTCCCTCCTGCCAGCAAGTTTTCTCTCACCT CCTGCTCTCATCTACTCCCTCTTGCCCCCAAGCCCTCCCTCCTGCCAGCAAGTTTTCTCTCACCT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36526166..36526458 26863196 MeRIP-seq:(Medium) rs1223719890 Functional Loss SNV dbSNP153 33..33 33 - - - 108523 RMVar_ID_108523 Human_SNP_ID_623149755 m1A Human chr17 - 36532156 36532156 36532156 CCTTGAAGCTAAGCCTTAAAGAACTAGAAAGAATTAGCCACTTGGAGAAGGAAAATAAGCACTCC CCTTGAAGCTAAGCCTTAAAGAACTAGAAAGAGTTAGCCACTTGGAGAAGGAAAATAAGCACTCC T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:36532150..36532299 26863196 MeRIP-seq:(Medium) rs1410516934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9857360,Human_RBP_ID_12977512,Human_RBP_ID_20205113,Human_RBP_ID_22950313 108524 RMVar_ID_108524 Human_SNP_ID_623149777 m1A Human chr17 + 36532271 36532271 36532271 GTGGCAGGGACATCTCTCAGGACTTCCTCTGCAGAATCCCCAAAGTGCCCTAAGGATTCCCTTAC GTGGCAGGGACATCTCTCAGGACTTCCTCTGCGGAATCCCCAAAGTGCCCTAAGGATTCCCTTAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36532223..36532308 26863196 MeRIP-seq:(Medium) rs73276799 Functional Loss SNV dbSNP153 33..33 33 - - - 108525 RMVar_ID_108525 Human_SNP_ID_623149882 m1A Human chr17 + 36532602 36532602 36532602 GTTGCAGGAGGTACAAGGAGTACTATCCACCTAGTCATGGGACCATGGGCTGGGGTATGGTTCCA GTTGCAGGAGGTACAAGGAGTACTATCCACCTCGTCATGGGACCATGGGCTGGGGTATGGTTCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36532551..36532679 26863196 MeRIP-seq:(Medium) rs1168989354 Functional Loss SNV dbSNP153 33..33 33 - - - 108526 RMVar_ID_108526 Human_SNP_ID_623150308 m1A Human chr17 - 36534106 36534105 36534107 CATTTACTCATTACCGTCTCCTTTCTGCCCACAGTGTTCACACCCTTTCCAGAAATTCTTGGCTG CATTTACTCATTACCGTCTCCTTTCTGCCCA__GTGTTCACACCCTTTCCAGAAATTCTTGGCTG CTG C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:36534051..36534173 26863410 MeRIP-seq:(Medium) rs1402795816 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_903069,Human_RBP_ID_4465306,Human_RBP_ID_22543140 108527 RMVar_ID_108527 Human_SNP_ID_623150309 m1A Human chr17 - 36534106 36534106 36534106 CATTTACTCATTACCGTCTCCTTTCTGCCCACAGTGTTCACACCCTTTCCAGAAATTCTTGGCTG CATTTACTCATTACCGTCTCCTTTCTGCCCACGGTGTTCACACCCTTTCCAGAAATTCTTGGCTG T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:36534051..36534173 26863410 MeRIP-seq:(Medium) rs1409362549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903069,Human_RBP_ID_4465306,Human_RBP_ID_22543140 108528 RMVar_ID_108528 Human_SNP_ID_623150535 m1A Human chr17 - 36534724 36534724 36534724 GTGTCAACCCGAACCTATATCTGAAGCCCTTCAGACGCGGAAGGGGCTTGGGAGGCCAGTTTGCC GTGTCAACCCGAACCTATATCTGAAGCCCTTCCGACGCGGAAGGGGCTTGGGAGGCCAGTTTGCC T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:36534721..36534913 26863196 MeRIP-seq:(Medium) rs527419233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1807165,Human_Splice_Rec_1807197 108529 RMVar_ID_108529 Human_SNP_ID_623150720 m1A Human chr17 - 36535056 36535056 36535056 CCTCATTTTACCCCAGGGTCGCAAAACATCTCACCGTAGTTGAAGCCAGCAAGCCGGACCAGGCG CCTCATTTTACCCCAGGGTCGCAAAACATCTCGCCGTAGTTGAAGCCAGCAAGCCGGACCAGGCG T C MYO19 Ensembl:ENSG00000278259 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36535050..36535172 26863196 MeRIP-seq:(Medium) rs1013934062 Functional Loss SNV dbSNP153 33..33 33 - - - 108530 RMVar_ID_108530 Human_SNP_ID_623150733 m1A Human chr17 + 36535093 36535093 36535093 TGTTTTGCGACCCTGGGGTAAAATGAGGGTAAAGCGGCAGCTTCCCACGTTCTGGGGGAGAAGCG TGTTTTGCGACCCTGGGGTAAAATGAGGGTAAGGCGGCAGCTTCCCACGTTCTGGGGGAGAAGCG A G PIGW Ensembl:ENSG00000277161 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36535042..36535184 26863196 MeRIP-seq:(Medium) rs1474948183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420788,Human_RBP_ID_5144113 108531 RMVar_ID_108531 Human_SNP_ID_623150764 m1A Human chr17 - 36535166 36535166 36535166 TCCGCCGCGGCGACCTCTACTGAAAGACCCCCAGTCCTGGTGTCGCCCGAAGGCCCAGGAAACCG TCCGCCGCGGCGACCTCTACTGAAAGACCCCCCGTCCTGGTGTCGCCCGAAGGCCCAGGAAACCG T G MYO19 Ensembl:ENSG00000278259 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36535069..36535249 26863196 MeRIP-seq:(Medium) rs1055996004 Functional Loss SNV dbSNP153 33..33 33 - - - 108532 RMVar_ID_108532 Human_SNP_ID_623150766 m1A Human chr17 + 36535181 36535181 36535181 TCGGGCGACACCAGGACTGGGGGTCTTTCAGTAGAGGTCGCCGCGGCGGAGTCTTGTGCGAGTGC TCGGGCGACACCAGGACTGGGGGTCTTTCAGTGGAGGTCGCCGCGGCGGAGTCTTGTGCGAGTGC A G PIGW Ensembl:ENSG00000277161 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:36535142..36535345 26863196 MeRIP-seq:(Medium) rs1027503802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420794,Human_RBP_ID_12977564 108533 RMVar_ID_108533 Human_SNP_ID_623154019 m1A Human chr17 + 36545659 36545638 36545659 TGGGAGGAGGCGGCAGCGGCGGCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAG TGGGAGGAGGCG_____________________GCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAG GGCAGCGGCGGCGGCAGAAACA G GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:36544951..36545825 26863196 MeRIP-seq:(Medium) rs1366786146 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_18419578 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 108534 RMVar_ID_108534 Human_SNP_ID_623154046 m1A Human chr17 + 36545680 36545671 36545680 GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA GCGGCAGAAACAGCAGCGGCGGCG_________GCTGGGAGGAGGTGGTGACGGTGGCAACGGCA GGCGGCGGCA G GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36545601..36545757 26863196 MeRIP-seq:(Medium) rs1227039407 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4420872,Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_9375729,Human_RBP_ID_17890428,Human_RBP_ID_18419578,Human_RBP_ID_22445400 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 108535 RMVar_ID_108535 Human_SNP_ID_623154051 m1A Human chr17 + 36545680 36545680 36545680 GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCCGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA A C GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36545601..36545757 26863196 MeRIP-seq:(Medium) rs1172001490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420872,Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_9375729,Human_RBP_ID_17890428,Human_RBP_ID_18419578,Human_RBP_ID_22445400 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 108536 RMVar_ID_108536 Human_SNP_ID_623154052 m1A Human chr17 + 36545680 36545680 36545680 GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCTGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA A T GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36545601..36545757 26863196 MeRIP-seq:(Medium) rs1172001490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420872,Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_9375729,Human_RBP_ID_17890428,Human_RBP_ID_18419578,Human_RBP_ID_22445400 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 108537 RMVar_ID_108537 Human_SNP_ID_623157564 m1A Human chr17 + 36557690 36557690 36557690 GAGCAAGCAAATCTTGTAGAAAACTGGGGGGAAGGCAGAGAAGGGACAGCTAGTGTAAAGGTTCT GAGCAAGCAAATCTTGTAGAAAACTGGGGGGATGGCAGAGAAGGGACAGCTAGTGTAAAGGTTCT A T GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:36557652..36557750 26863196 MeRIP-seq:(Medium) rs1183984597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65606,RMVar_hsa_circ_316137,RMVar_hsa_circ_315183,RMVar_hsa_circ_183720,RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_312387,RMVar_hsa_circ_288673 108538 RMVar_ID_108538 Human_SNP_ID_623167196 m1A Human chr17 + 36591917 36591917 36591917 CTGGTGGGTCTAGGCGCGGATCGGACCCAAGCAGGTCGGCGGCGGCGGCAGGAGAGCGGCCGGGC CTGGTGGGTCTAGGCGCGGATCGGACCCAAGCGGGTCGGCGGCGGCGGCAGGAGAGCGGCCGGGC A G DHRS11 Ensembl:ENSG00000278535 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36591851..36592175 26863196 MeRIP-seq:(Medium) rs1249771270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465310,Human_RBP_ID_22959398 108539 RMVar_ID_108539 Human_SNP_ID_623167209 m1A Human chr17 + 36591934 36591934 36591934 GGATCGGACCCAAGCAGGTCGGCGGCGGCGGCAGGAGAGCGGCCGGGCGTCAGCTCCTCGACCCC GGATCGGACCCAAGCAGGTCGGCGGCGGCGGCGGGAGAGCGGCCGGGCGTCAGCTCCTCGACCCC A G DHRS11 Ensembl:ENSG00000278535 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:36591865..36592175 26863196 MeRIP-seq:(Medium) rs890474162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4420943,Human_RBP_ID_5366763,Human_RBP_ID_22959398 108540 RMVar_ID_108540 Human_SNP_ID_623167570 m1A Human chr17 + 36593338 36593338 36593338 CCCTGTTGTGAGGGGGTGACATGATGTTGTAGATCATTACTGAGGGGAGGTAGGGAGATCAGGTG CCCTGTTGTGAGGGGGTGACATGATGTTGTAGGTCATTACTGAGGGGAGGTAGGGAGATCAGGTG A G DHRS11 Ensembl:ENSG00000278535 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:36593335..36593465 26863196 MeRIP-seq:(Medium) rs756682511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6587185,Human_RBP_ID_12978272 108541 RMVar_ID_108541 Human_SNP_ID_623169347 m1A Human chr17 + 36600565 36600565 36600565 CCTCAACGTCTGTGGCTCAGGGCTGGGGTGGCAGAGGGAGGCCTTCACCTTATATCTGTGTTGTT CCTCAACGTCTGTGGCTCAGGGCTGGGGTGGCGGAGGGAGGCCTTCACCTTATATCTGTGTTGTT A G DHRS11 Ensembl:ENSG00000278535 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:36600457..36600756 32194978 MeRIP-seq:(Medium) rs1567844047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1855970,Human_RBP_ID_17259334,Human_RBP_ID_17890463,Human_RBP_ID_18941591 Human_miRNA_ID_2956369 RMVar_hsa_circ_183728,RMVar_hsa_circ_122952,RMVar_hsa_circ_96014,RMVar_hsa_circ_183729 108542 RMVar_ID_108542 Human_SNP_ID_623258533 m1A Human chr17 + 36949104 36949104 36949104 GGTTGGGCCGCACATTTACGTGCGCGAAGCGGAGTGGACCGGGAGCTGGTGACGATGGCGGGGCC GGTTGGGCCGCACATTTACGTGCGCGAAGCGGTGTGGACCGGGAGCTGGTGACGATGGCGGGGCC A T AATF Ensembl:ENSG00000275700 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36948951..36950445 26863196 MeRIP-seq:(Medium) rs761827493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6310,Human_RBP_ID_49824,Human_RBP_ID_237245,Human_RBP_ID_903102,Human_RBP_ID_4465312,Human_RBP_ID_5525516,Human_RBP_ID_6587372,Human_RBP_ID_8816706,Human_RBP_ID_9288985,Human_RBP_ID_9326577,Human_RBP_ID_9375734,Human_RBP_ID_18164192,Human_RBP_ID_18419579,Human_RBP_ID_18438802,Human_RBP_ID_22061255,Human_RBP_ID_26331630,Human_RBP_ID_26769504,Human_RBP_ID_26959402,Human_RBP_ID_27813741 108543 RMVar_ID_108543 Human_SNP_ID_623258542 m1A Human chr17 + 36949115 36949115 36949115 ACATTTACGTGCGCGAAGCGGAGTGGACCGGGAGCTGGTGACGATGGCGGGGCCGCAGCCCCTGG ACATTTACGTGCGCGAAGCGGAGTGGACCGGGTGCTGGTGACGATGGCGGGGCCGCAGCCCCTGG A T AATF Ensembl:ENSG00000275700 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36949019..36949179 26863196 MeRIP-seq:(Medium) rs1471972531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6310,Human_RBP_ID_49824,Human_RBP_ID_237245,Human_RBP_ID_903102,Human_RBP_ID_1181476,Human_RBP_ID_4465312,Human_RBP_ID_5525516,Human_RBP_ID_6587372,Human_RBP_ID_8816706,Human_RBP_ID_9288985,Human_RBP_ID_9326577,Human_RBP_ID_9375734,Human_RBP_ID_18164192,Human_RBP_ID_18419579,Human_RBP_ID_18438802,Human_RBP_ID_22061255,Human_RBP_ID_26331630,Human_RBP_ID_26769504,Human_RBP_ID_26959402,Human_RBP_ID_27813741 108544 RMVar_ID_108544 Human_SNP_ID_623259602 m1A Human chr17 + 36953145 36953145 36953145 GAGGAGGAGGAAGACGAAGAGAGTGGCATGGAAGAAGGGGATGACGCGGAAGACTCCCAAGGCGA GAGGAGGAGGAAGACGAAGAGAGTGGCATGGACGAAGGGGATGACGCGGAAGACTCCCAAGGCGA A C AATF Ensembl:ENSG00000275700 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:36952893..36953275 26863196 MeRIP-seq:(Medium) rs1389694367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49827,Human_RBP_ID_237246,Human_RBP_ID_822033,Human_RBP_ID_6587391,Human_RBP_ID_8450409,Human_RBP_ID_9375736,Human_RBP_ID_18411892,Human_RBP_ID_23118755,Human_RBP_ID_23722608,Human_RBP_ID_24544847,Human_RBP_ID_26331634,Human_RBP_ID_27813744 Human_miRNA_ID_2897135 RMVar_hsa_circ_51709,RMVar_hsa_circ_283762,RMVar_hsa_circ_69472,RMVar_hsa_circ_183731 108545 RMVar_ID_108545 Human_SNP_ID_623268524 m1A Human chr17 - 36990803 36990803 36990803 TCAAAGATTTCTTCATCCAAGTCCTTCAGATGAGCATTAGCAGGGGCTTGAGGAAGGATCTCCTA TCAAAGATTTCTTCATCCAAGTCCTTCAGATGGGCATTAGCAGGGGCTTGAGGAAGGATCTCCTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36990776..36990850 32194978 MeRIP-seq:(Medium) rs372723663 Functional Loss SNV dbSNP153 33..33 33 - - - 108546 RMVar_ID_108546 Human_SNP_ID_623275084 m1A Human chr17 + 37019065 37019065 37019065 CCAGCTCCTTGGATCCCAACGATCAGGTGGCCATGGGAAGGTAATTTAGATACAGCTTTCTGTTC CCAGCTCCTTGGATCCCAACGATCAGGTGGCCGTGGGAAGGTAATTTAGATACAGCTTTCTGTTC A G AATF Ensembl:ENSG00000275700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:37019037..37020999 32194978 MeRIP-seq:(Medium) rs781439292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_905362,Human_RBP_ID_18988240,Human_RBP_ID_26331640 Human_Splice_Rec_1807440,Human_Splice_Rec_1807441,Human_Splice_Rec_1807458,Human_Splice_Rec_1807459,Human_Splice_Rec_1807462,Human_Splice_Rec_1807463,Human_Splice_Rec_1807467 RMVar_hsa_circ_38948,RMVar_hsa_circ_280468,RMVar_hsa_circ_69044,RMVar_hsa_circ_309119 108547 RMVar_ID_108547 Human_SNP_ID_623283920 m1A Human chr17 - 37056722 37056722 37056722 AGCTCAGCCCCATAAAGTCACTGGTTTCCTCCATCTGGACCAGCAGCCGCACCAGCCAAGGCGCC AGCTCAGCCCCATAAAGTCACTGGTTTCCTCCCTCTGGACCAGCAGCCGCACCAGCCAAGGCGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:37056672..37056821 32194978 MeRIP-seq:(Medium) rs1397955957 Functional Loss SNV dbSNP153 33..33 33 - - - 108548 RMVar_ID_108548 Human_SNP_ID_623366712 m1A Human chr17 + 37406686 37406684 37406686 CCACACGGGCAAAGTGATTACTGGTCGGATCAAAAGTCAGGCAAGCGGCTCAGCCCCATCCTCCC CCACACGGGCAAAGTGATTACTGGTCGGATC__AAGTCAGGCAAGCGGCTCAGCCCCATCCTCCC CAA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37406636..37406795 26863196 MeRIP-seq:(Medium) rs1271226572 Functional Loss DEL dbSNP153 32..33 33 - - - 108549 RMVar_ID_108549 Human_SNP_ID_623366848 m1A Human chr17 - 37406951 37406951 37406951 CCGCCCGCCCGCCCAGCGCTGCCTGGCGCCTCACCTCGCCGAGACCCCCTAATCCGCGCCAAAGA CCGCCCGCCCGCCCAGCGCTGCCTGGCGCCTCCCCTCGCCGAGACCCCCTAATCCGCGCCAAAGA T G lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37406914..37407126 26863196 MeRIP-seq:(Medium) rs1046899546 Functional Loss SNV dbSNP153 33..33 33 - - - 108550 RMVar_ID_108550 Human_SNP_ID_623385736 m1A Human chr17 + 37479197 37479194 37479198 GGCAGATGGAAGTGGGAGACAATTCCACACACAGGGGGTGGAGAATGATGTGGAGGCAGCAGTGG GGCAGATGGAAGTGGGAGACAATTCCACAC____GGGGTGGAGAATGATGTGGAGGCAGCAGTGG CACAG C TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37479147..37479278 26863196 MeRIP-seq:(Medium) rs752493445 Functional Loss DEL dbSNP153 31..34 33 - - - 108551 RMVar_ID_108551 Human_SNP_ID_623385738 m1A Human chr17 + 37479197 37479196 37479198 GGCAGATGGAAGTGGGAGACAATTCCACACACAGGGGGTGGAGAATGATGTGGAGGCAGCAGTGG GGCAGATGGAAGTGGGAGACAATTCCACACAC__GGGGTGGAGAATGATGTGGAGGCAGCAGTGG CAG C TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37479147..37479278 26863196 MeRIP-seq:(Medium) rs142040516 Functional Loss DEL dbSNP153 33..34 33 - - - 108552 RMVar_ID_108552 Human_SNP_ID_623388518 m1A Human chr17 - 37489940 37489935 37489940 TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGGAGCGGGTTGCGGTTAGGGCTCCGTCCTCCTGCG TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGG_____GTTGCGGTTAGGGCTCCGTCCTCCTGCG CCCGCT C lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:37489851..37491486;chr17:37489846..37491486 26863196 MeRIP-seq:(Medium) rs373703160 Functional Loss DEL dbSNP153 33..37 33 - - - 108553 RMVar_ID_108553 Human_SNP_ID_623388527 m1A Human chr17 - 37489940 37489940 37489940 TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGGAGCGGGTTGCGGTTAGGGCTCCGTCCTCCTGCG TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGGGGCGGGTTGCGGTTAGGGCTCCGTCCTCCTGCG T C lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:37489851..37491486;chr17:37489846..37491486 26863196 MeRIP-seq:(Medium) rs1555695791 Functional Loss SNV dbSNP153 33..33 33 - - - 108554 RMVar_ID_108554 Human_SNP_ID_623388528 m1A Human chr17 - 37489940 37489940 37489940 TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGGAGCGGGTTGCGGTTAGGGCTCCGTCCTCCTGCG TGCGGGTCCCCTACCGGCGCGGCGCGGCGCGGCGCGGGTTGCGGTTAGGGCTCCGTCCTCCTGCG T G lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:37489851..37491486;chr17:37489846..37491486 26863196 MeRIP-seq:(Medium) rs1555695791 Functional Loss SNV dbSNP153 33..33 33 - - - 108555 RMVar_ID_108555 Human_SNP_ID_623394174 m1A Human chr17 - 37510728 37510728 37510728 TCAAGAGTCCAGTGTGCGCTGCCTGGGTCCGGATCCAGAAAGTCCTAAGTGAGCAGTGCTGGTGA TCAAGAGTCCAGTGTGCGCTGCCTGGGTCCGGTTCCAGAAAGTCCTAAGTGAGCAGTGCTGGTGA T A lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:37510673..37512271 26863196 MeRIP-seq:(Medium) rs1207432290 Functional Loss SNV dbSNP153 33..33 33 - - - 108556 RMVar_ID_108556 Human_SNP_ID_623394762 m1A Human chr17 + 37512403 37512403 37512403 TCTATTCCTGGGCAGAGGCAGTGTGGCCTCCAATCGGCACCTCCTCCAGGCTCGTGGCATCACCT TCTATTCCTGGGCAGAGGCAGTGTGGCCTCCAGTCGGCACCTCCTCCAGGCTCGTGGCATCACCT A G lnc-HNF1B-3 RNACentral:URS0000D57167 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs759100584 Functional Loss SNV dbSNP153 33..33 33 - - - 108557 RMVar_ID_108557 Human_SNP_ID_623418540 m1A Human chr17 - 37609026 37609026 37609026 CGAGCGGGGAGCGAGCGCGCGCCCAGTGTGGGAGGGGAGAGAAGATGAGGGTCCTCTTGGGGTGG CGAGCGGGGAGCGAGCGCGCGCCCAGTGTGGGGGGGGAGAGAAGATGAGGGTCCTCTTGGGGTGG T C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37609022..37609087 26863196 MeRIP-seq:(Medium) rs1213669305 Functional Loss SNV dbSNP153 33..33 33 - - - 108558 RMVar_ID_108558 Human_SNP_ID_623418541 m1A Human chr17 - 37609026 37609026 37609026 CGAGCGGGGAGCGAGCGCGCGCCCAGTGTGGGAGGGGAGAGAAGATGAGGGTCCTCTTGGGGTGG CGAGCGGGGAGCGAGCGCGCGCCCAGTGTGGGCGGGGAGAGAAGATGAGGGTCCTCTTGGGGTGG T G SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:37609022..37609087 26863196 MeRIP-seq:(Medium) rs1213669305 Functional Loss SNV dbSNP153 33..33 33 - - - 108559 RMVar_ID_108559 Human_SNP_ID_623534262 m1A Human chr17 + 38256406 38256406 38256406 TCGCTCCAACGCGGCGGCCAGAGTCCCAAATGACCACTCCCTCCAATCTATCACCCGAGAGGTGT TCGCTCCAACGCGGCGGCCAGAGTCCCAAATGGCCACTCCCTCCAATCTATCACCCGAGAGGTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:38256366..38256505;chr17:38256388..38256486 26863196 MeRIP-seq:(Medium) rs1375521684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18438837 108560 RMVar_ID_108560 Human_SNP_ID_623534641 m1A Human chr17 + 38257177 38257174 38257177 AGCCACATCCACCGAGCGCGGGCGACCGCCGGAGGAGAGCGACCGGGGGAGCCTGGGGGGCGGGG AGCCACATCCACCGAGCGCGGGCGACCGCC___GGAGAGCGACCGGGGGAGCCTGGGGGGCGGGG CGGA C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:38257076..38257275 26863410 MeRIP-seq:(Medium) rs1343526961 Functional Loss DEL dbSNP153 31..33 33 - - - 108561 RMVar_ID_108561 Human_SNP_ID_623534665 m1A Human chr17 + 38257231 38257231 38257231 GGGGGGCGGGGGAGAGACCCAGCCGGAGCGCTAGGGGTTGGGAAGGAGGCGGTGCGGGCGGACTG GGGGGGCGGGGGAGAGACCCAGCCGGAGCGCTGGGGGTTGGGAAGGAGGCGGTGCGGGCGGACTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chr17:38257122..38257254;chr17:38257137..38257275 26863196,26863410 MeRIP-seq:(Medium) rs1334239029 Functional Loss SNV dbSNP153 33..33 33 - - - 108562 RMVar_ID_108562 Human_SNP_ID_623534671 m1A Human chr17 - 38257237 38257237 38257237 GCCCGCCAGTCCGCCCGCACCGCCTCCTTCCCAACCCCTAGCGCTCCGGCTGGGTCTCTCCCCCG GCCCGCCAGTCCGCCCGCACCGCCTCCTTCCCCACCCCTAGCGCTCCGGCTGGGTCTCTCCCCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr17:38257181..38257344;chr17:38257122..38257281;chr17:38257116..38257329;chr17:38257182..38257372 26863196 MeRIP-seq:(Medium) rs1187911702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768783,Human_RBP_ID_25278212 108563 RMVar_ID_108563 Human_SNP_ID_623534673 m1A Human chr17 + 38257245 38257245 38257245 AGACCCAGCCGGAGCGCTAGGGGTTGGGAAGGAGGCGGTGCGGGCGGACTGGCGGGCGAGCTGCC AGACCCAGCCGGAGCGCTAGGGGTTGGGAAGGGGGCGGTGCGGGCGGACTGGCGGGCGAGCTGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38257165..38257375 26863196 MeRIP-seq:(Medium) rs1385080766 Functional Loss SNV dbSNP153 33..33 33 - - - 108564 RMVar_ID_108564 Human_SNP_ID_623544918 m1A Human chr17 + 38297196 38297196 38297196 GCGGCCTTTGCGGGAACAAGATGGCAGCCCCCATACCTCAAGGGTTCTCTTGTTTATCGAGGTTT GCGGCCTTTGCGGGAACAAGATGGCAGCCCCCGTACCTCAAGGGTTCTCTTGTTTATCGAGGTTT A G MRPL45 Ensembl:ENSG00000278845 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38297181..38297308 26863196 MeRIP-seq:(Medium) rs1179413434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1181566,Human_RBP_ID_4465315,Human_RBP_ID_6589708,Human_RBP_ID_18696050 Human_Splice_Rec_1809243,Human_Splice_Rec_1809255 108565 RMVar_ID_108565 Human_SNP_ID_623544939 m1A Human chr17 - 38297226 38297226 38297226 CCTACCCACCTGCCGAGACCACCAGCCCAAAAACCTCGATAAACAAGAGAACCCTTGAGGTATGG CCTACCCACCTGCCGAGACCACCAGCCCAAAAGCCTCGATAAACAAGAGAACCCTTGAGGTATGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38297217..38298514 32194978 MeRIP-seq:(Medium) rs9890011 Functional Loss SNV dbSNP153 33..33 33 - - - 108566 RMVar_ID_108566 Human_SNP_ID_623544940 m1A Human chr17 - 38297226 38297226 38297226 CCTACCCACCTGCCGAGACCACCAGCCCAAAAACCTCGATAAACAAGAGAACCCTTGAGGTATGG CCTACCCACCTGCCGAGACCACCAGCCCAAAACCCTCGATAAACAAGAGAACCCTTGAGGTATGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38297217..38298514 32194978 MeRIP-seq:(Medium) rs9890011 Functional Loss SNV dbSNP153 33..33 33 - - - 108567 RMVar_ID_108567 Human_SNP_ID_623544955 m1A Human chr17 - 38297251 38297251 38297251 CCCCTAGGGTCCTATCGGCCCCGTCCCTACCCACCTGCCGAGACCACCAGCCCAAAAACCTCGAT CCCCTAGGGTCCTATCGGCCCCGTCCCTACCCCCCTGCCGAGACCACCAGCCCAAAAACCTCGAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38297211..38297295 26863196 MeRIP-seq:(Medium) rs758842244 Functional Loss SNV dbSNP153 33..33 33 - - - 108568 RMVar_ID_108568 Human_SNP_ID_623560375 m1A Human chr17 - 38352265 38352265 38352265 GCCGCCTCCACGTCCTCCTCCTCCGGCGGCCGACCCACGTTGCGGAACACCATCAGCTGCGGCGG GCCGCCTCCACGTCCTCCTCCTCCGGCGGCCGCCCCACGTTGCGGAACACCATCAGCTGCGGCGG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38352219..38352348 26863196 MeRIP-seq:(Medium) rs1259204134 Functional Loss SNV dbSNP153 33..33 33 - - - 108569 RMVar_ID_108569 Human_SNP_ID_623560380 m1A Human chr17 + 38352276 38352273 38352276 GATGGTGTTCCGCAACGTGGGTCGGCCGCCGGAGGAGGAGGACGTGGAGGCGGCCCCGGAGCCGG GATGGTGTTCCGCAACGTGGGTCGGCCGCC___GGAGGAGGACGTGGAGGCGGCCCCGGAGCCGG CGGA C SOCS7 Ensembl:ENSG00000274211 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38352225..38352375 26863196 MeRIP-seq:(Medium) rs758404350 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_6589809,Human_RBP_ID_17691868 108570 RMVar_ID_108570 Human_SNP_ID_623560479 m1A Human chr17 + 38352507 38352507 38352507 TGGGGGTTGCTGCCCGTGTCCGTGTCCTCCTCAGCCGCCCCCTCCGCAGCCCCAGCCGCCTGCTG TGGGGGTTGCTGCCCGTGTCCGTGTCCTCCTCTGCCGCCCCCTCCGCAGCCCCAGCCGCCTGCTG A T SOCS7 Ensembl:ENSG00000274211 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38352460..38352635 26863196 MeRIP-seq:(Medium) rs1260731832 Functional Loss SNV dbSNP153 33..33 33 - - - 108571 RMVar_ID_108571 Human_SNP_ID_623586614 m1A Human chr17 + 38453850 38453850 38453850 CCGGGGCCCGCCGGCCGCCCGGGGGGTCGAGGACGCCGTCTGCCGGGCGCCTAGCAGCGGCCCCG CCGGGGCCCGCCGGCCGCCCGGGGGGTCGAGGGCGCCGTCTGCCGGGCGCCTAGCAGCGGCCCCG A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38453749..38453865 26863196 MeRIP-seq:(Medium) rs1242415540 Functional Loss SNV dbSNP153 33..33 33 - - - 108572 RMVar_ID_108572 Human_SNP_ID_623586710 m1A Human chr17 + 38454175 38454175 38454175 GAGAGCCGCGGGGCCGGGGCCGGGGCCGGGGCAGGCCTTGTCGGGGTCTGAGTGGGACTGGGTCA GAGAGCCGCGGGGCCGGGGCCGGGGCCGGGGCTGGCCTTGTCGGGGTCTGAGTGGGACTGGGTCA A T ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38454154..38454285 26863196 MeRIP-seq:(Medium) rs1160851605 Functional Loss SNV dbSNP153 33..33 33 - - - 108573 RMVar_ID_108573 Human_SNP_ID_623590051 m1A Human chr17 - 38466695 38466695 38466695 TCGGTGCCAGCCCTCCTGGCCCAGCTGGCTCAAAGCATCCTGGGAGGTGGAGCAGGGCCACGGGC TCGGTGCCAGCCCTCCTGGCCCAGCTGGCTCAGAGCATCCTGGGAGGTGGAGCAGGGCCACGGGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38466646..38466797 32194978 MeRIP-seq:(Medium) rs1413231544 Functional Loss SNV dbSNP153 33..33 33 - - - 108574 RMVar_ID_108574 Human_SNP_ID_623590215 m1A Human chr17 - 38467035 38467035 38467035 CCTCTGGTGGGAATGACGCAGGGGACTGGGCCAGGTTGAAGGTAGGCAGCCCCCCAAAGGGTGAG CCTCTGGTGGGAATGACGCAGGGGACTGGGCCGGGTTGAAGGTAGGCAGCCCCCCAAAGGGTGAG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38466825..38467085 26863196 MeRIP-seq:(Medium) rs1156474866 Functional Loss SNV dbSNP153 33..33 33 - - - 108575 RMVar_ID_108575 Human_SNP_ID_623590775 m1A Human chr17 - 38469234 38469234 38469234 AAGTGAAGGTCGGGGAAGATGGGCTGGTGCCCAGGACAGGGGCTGAGTTCATGGCACTGGAGACC AAGTGAAGGTCGGGGAAGATGGGCTGGTGCCCGGGACAGGGGCTGAGTTCATGGCACTGGAGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38469186..38469269 26863196 MeRIP-seq:(Medium) rs1448640781 Functional Loss SNV dbSNP153 33..33 33 - - - 108576 RMVar_ID_108576 Human_SNP_ID_623591033 m1A Human chr17 - 38469891 38469891 38469891 ACACACTTGCAGCTCTCACCCCGTCGGTGAAGAAGCTCCGGAGCATCCGCAGGCTGGGTATGCGG ACACACTTGCAGCTCTCACCCCGTCGGTGAAGTAGCTCCGGAGCATCCGCAGGCTGGGTATGCGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38469630..38477672 32194978 MeRIP-seq:(Medium) rs1245719091 Functional Loss SNV dbSNP153 33..33 33 - - - 108577 RMVar_ID_108577 Human_SNP_ID_623592257 m1A Human chr17 + 38474365 38474364 38474366 ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGCAGACACTTTAGAGAGAGATTCCAGGGGAAGGAG ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGC__ACACTTTAGAGAGAGATTCCAGGGGAAGGAG CAG C ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38474315..38474430 26863196 MeRIP-seq:(Medium) rs1429909875 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_39373,RMVar_hsa_circ_92993,RMVar_hsa_circ_183798 108578 RMVar_ID_108578 Human_SNP_ID_623592258 m1A Human chr17 + 38474365 38474365 38474365 ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGCAGACACTTTAGAGAGAGATTCCAGGGGAAGGAG ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGCGGACACTTTAGAGAGAGATTCCAGGGGAAGGAG A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38474315..38474430 26863196 MeRIP-seq:(Medium) rs558987492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39373,RMVar_hsa_circ_92993,RMVar_hsa_circ_183798 108579 RMVar_ID_108579 Human_SNP_ID_623592259 m1A Human chr17 + 38474365 38474365 38474365 ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGCAGACACTTTAGAGAGAGATTCCAGGGGAAGGAG ACCCAAGGCAGTGGTGTGAGGCCGGGTGGAGCTGACACTTTAGAGAGAGATTCCAGGGGAAGGAG A T ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38474315..38474430 26863196 MeRIP-seq:(Medium) rs558987492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39373,RMVar_hsa_circ_92993,RMVar_hsa_circ_183798 108580 RMVar_ID_108580 Human_SNP_ID_623592727 m1A Human chr17 + 38476522 38476522 38476522 GCCTGGCAAGTATTGTGCAAAGTGCCCATGGGACCTGCAAATGAAGCCACTGAGCAGGGTGGGGG GCCTGGCAAGTATTGTGCAAAGTGCCCATGGGGCCTGCAAATGAAGCCACTGAGCAGGGTGGGGG A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38476518..38476639 26863196 MeRIP-seq:(Medium) rs1423187393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39373,RMVar_hsa_circ_92993,RMVar_hsa_circ_183798 108581 RMVar_ID_108581 Human_SNP_ID_623592820 m1A Human chr17 + 38476924 38476924 38476924 AGGTGTAGAGGGTGGGGGAGGGCAAGTAGAGAAGACTAGGAAGGAGCCAGTGGCATTAGGAAGAA AGGTGTAGAGGGTGGGGGAGGGCAAGTAGAGAGGACTAGGAAGGAGCCAGTGGCATTAGGAAGAA A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38476900..38477103 26863196 MeRIP-seq:(Medium) rs923465816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39373,RMVar_hsa_circ_92993,RMVar_hsa_circ_183798 108582 RMVar_ID_108582 Human_SNP_ID_623599304 m1A Human chr17 + 38503140 38503140 38503140 ATGATCCAGGTGAGAGACAGAGAGAGAGAGGAAGAGCTGGGCCCAGAGCCCGTGAAGCAGCAGTA ATGATCCAGGTGAGAGACAGAGAGAGAGAGGAGGAGCTGGGCCCAGAGCCCGTGAAGCAGCAGTA A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38503137..38503293 26863196 MeRIP-seq:(Medium) rs1321817871 Functional Loss SNV dbSNP153 33..33 33 - - - 108583 RMVar_ID_108583 Human_SNP_ID_623600590 m1A Human chr17 + 38508548 38508548 38508548 CAAGCTTCTGAGCAAAGCTGGGTGAGGATCAGATTCCTGCTTCAGAATGGTGGCTCTGGAGGAGA CAAGCTTCTGAGCAAAGCTGGGTGAGGATCAGGTTCCTGCTTCAGAATGGTGGCTCTGGAGGAGA A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38508543..38508864 26863196 MeRIP-seq:(Medium) rs747357091 Functional Loss SNV dbSNP153 33..33 33 - - - 108584 RMVar_ID_108584 Human_SNP_ID_623600996 m1A Human chr17 - 38509998 38509996 38509999 CTTCTTGCGCTTGCGGTTGACGGCCGAGATGAAGGAGATCGCCAGCATCTCCCGGGCGTACGGCT CTTCTTGCGCTTGCGGTTGACGGCCGAGATG___GAGATCGCCAGCATCTCCCGGGCGTACGGCT CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38509946..38510197 32194978 MeRIP-seq:(Medium) rs1308560679 Functional Loss DEL dbSNP153 32..34 33 - - - 108585 RMVar_ID_108585 Human_SNP_ID_623601136 m1A Human chr17 + 38510343 38510343 38510343 GGGATGAGGCGGACGACGAGCGTAGCGAGCTGAGCCACGTGGAGACGGACACTGAGGGCGCGGCG GGGATGAGGCGGACGACGAGCGTAGCGAGCTGGGCCACGTGGAGACGGACACTGAGGGCGCGGCG A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:38510251..38510376;chr17:38509944..38510488;chr17:38510158..38510406 26863196 MeRIP-seq:(Medium) rs1342951217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17890963 108586 RMVar_ID_108586 Human_SNP_ID_623601483 m1A Human chr17 + 38511139 38511137 38511140 CTCTAGTTGGTGTGCTGGAACTGGCAGGGCAGAGGAGAAGGCTGGGGCCGGACTAATTGAATGGA CTCTAGTTGGTGTGCTGGAACTGGCAGGGCA___GAGAAGGCTGGGGCCGGACTAATTGAATGGA AGAG A ARHGAP23 Ensembl:ENSG00000275832 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38511088..38511222 26863196 MeRIP-seq:(Medium) rs776527068 Functional Loss DEL dbSNP153 32..34 33 - - - 108587 RMVar_ID_108587 Human_SNP_ID_623601593 m1A Human chr17 - 38511484 38511484 38511484 GACAGAAGTCGCTACTGGAAACACCTTGGGACAATGACTGCACACACAAGCCCCTCCCCCCATGG GACAGAAGTCGCTACTGGAAACACCTTGGGACGATGACTGCACACACAAGCCCCTCCCCCCATGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38511434..38511544 26863196 MeRIP-seq:(Medium) rs961485041 Functional Loss SNV dbSNP153 33..33 33 - - - 108588 RMVar_ID_108588 Human_SNP_ID_623625480 m1A Human chr17 - 38605406 38605406 38605406 GAGGCAGGAGACTGGGTGGGGAGGGCCTCACTACGCCCCGGGGTGGGGGCCAGAGGGGTTCAACT GAGGCAGGAGACTGGGTGGGGAGGGCCTCACTTCGCCCCGGGGTGGGGGCCAGAGGGGTTCAACT T A SRCIN1 Ensembl:ENSG00000277363 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38605400..38605572 26863196 MeRIP-seq:(Medium) rs116364856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542893,Human_RBP_ID_5186132,Human_RBP_ID_8189584,Human_RBP_ID_9422305,Human_RBP_ID_18459643,Human_RBP_ID_18941612 108589 RMVar_ID_108589 Human_SNP_ID_623625481 m1A Human chr17 - 38605406 38605406 38605406 GAGGCAGGAGACTGGGTGGGGAGGGCCTCACTACGCCCCGGGGTGGGGGCCAGAGGGGTTCAACT GAGGCAGGAGACTGGGTGGGGAGGGCCTCACTGCGCCCCGGGGTGGGGGCCAGAGGGGTTCAACT T C SRCIN1 Ensembl:ENSG00000277363 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38605400..38605572 26863196 MeRIP-seq:(Medium) rs116364856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542893,Human_RBP_ID_5186132,Human_RBP_ID_8189584,Human_RBP_ID_9422305,Human_RBP_ID_18459643,Human_RBP_ID_18941612 108590 RMVar_ID_108590 Human_SNP_ID_623642932 m1A Human chr17 - 38673565 38673565 38673565 CCCGCCGCCCTGCACCGACGCTCCCCACCACGAGCACCTTCAGCCTCCTCAACTGCTTCCCCTGC CCCGCCGCCCTGCACCGACGCTCCCCACCACGTGCACCTTCAGCCTCCTCAACTGCTTCCCCTGC T A EPOP Ensembl:ENSG00000273604 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38673465..38673688 26863196 MeRIP-seq:(Medium) rs1361883527 Functional Loss SNV dbSNP153 33..33 33 - - - 108591 RMVar_ID_108591 Human_SNP_ID_623643289 m1A Human chr17 + 38674461 38674461 38674461 GGGAGCAGGGCGACCCTCGCGGGGACGCCGGCACTGCCAGGCGGGGCGCAGGGCACAGGGTCTCC GGGAGCAGGGCGACCCTCGCGGGGACGCCGGCCCTGCCAGGCGGGGCGCAGGGCACAGGGTCTCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38674411..38674495 26863196 MeRIP-seq:(Medium) rs1248116236 Functional Loss SNV dbSNP153 33..33 33 - - - 108592 RMVar_ID_108592 Human_SNP_ID_623643291 m1A Human chr17 - 38674463 38674463 38674463 ATGGAGACCCTGTGCCCTGCGCCCCGCCTGGCAGTGCCGGCGTCCCCGCGAGGGTCGCCCTGCTC ATGGAGACCCTGTGCCCTGCGCCCCGCCTGGCGGTGCCGGCGTCCCCGCGAGGGTCGCCCTGCTC T C EPOP Ensembl:ENSG00000273604 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38674413..38674898 26863196 MeRIP-seq:(Medium) rs1218841252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464478,Human_RBP_ID_22063097 108593 RMVar_ID_108593 Human_SNP_ID_623643336 m1A Human chr17 + 38674617 38674617 38674617 ATCGCCCCCCGTCGACGGGGAGGTCTCTGCTCACGGGCGCCCCCGGCCCGCCACCCGGGGCCGCA ATCGCCCCCCGTCGACGGGGAGGTCTCTGCTCCCGGGCGCCCCCGGCCCGCCACCCGGGGCCGCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38674577..38674901 26863196 MeRIP-seq:(Medium) rs891567590 Functional Loss SNV dbSNP153 33..33 33 - - - 108594 RMVar_ID_108594 Human_SNP_ID_623650930 m1A Human chr17 - 38705270 38705270 38705270 CCGAGCCCGGCGGGGGAGGCGCCGAGTGGCACATCGCGGGCGCCCGCCCGCCCCGCGCCGCCCCG CCGAGCCCGGCGGGGGAGGCGCCGAGTGGCACTTCGCGGGCGCCCGCCCGCCCCGCGCCGCCCCG T A AC006449.2 Ensembl:ENSG00000275532 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:38705201..38705284 26863410 MeRIP-seq:(Medium) rs1009273098 Functional Loss SNV dbSNP153 33..33 33 - - - 108595 RMVar_ID_108595 Human_SNP_ID_623650931 m1A Human chr17 - 38705270 38705270 38705270 CCGAGCCCGGCGGGGGAGGCGCCGAGTGGCACATCGCGGGCGCCCGCCCGCCCCGCGCCGCCCCG CCGAGCCCGGCGGGGGAGGCGCCGAGTGGCACGTCGCGGGCGCCCGCCCGCCCCGCGCCGCCCCG T C AC006449.2 Ensembl:ENSG00000275532 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:38705201..38705284 26863410 MeRIP-seq:(Medium) rs1009273098 Functional Loss SNV dbSNP153 33..33 33 - - - 108596 RMVar_ID_108596 Human_SNP_ID_623650970 m1A Human chr17 - 38705378 38705375 38705378 GCCCTCATGCCCCGACGGGCCCCCCCCACAACAATGAGACTCGCACGCCGGGCTCGCCCCCTCCG GCCCTCATGCCCCGACGGGCCCCCCCCACAAC___GAGACTCGCACGCCGGGCTCGCCCCCTCCG CATT C AC006449.2 Ensembl:ENSG00000275532 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38705177..38705550 26863196 MeRIP-seq:(Medium) rs1264756268 Functional Loss DEL dbSNP153 33..35 33 - - - 108597 RMVar_ID_108597 Human_SNP_ID_623650972 m1A Human chr17 - 38705378 38705376 38705379 GCCCTCATGCCCCGACGGGCCCCCCCCACAACAATGAGACTCGCACGCCGGGCTCGCCCCCTCCG GCCCTCATGCCCCGACGGGCCCCCCCCACAA___TGAGACTCGCACGCCGGGCTCGCCCCCTCCG ATTG A AC006449.2 Ensembl:ENSG00000275532 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38705177..38705550 26863196 MeRIP-seq:(Medium) rs1419341384 Functional Loss DEL dbSNP153 32..34 33 - - - 108598 RMVar_ID_108598 Human_SNP_ID_623650993 m1A Human chr17 + 38705406 38705406 38705406 TCATTGTTGTGGGGGGGGCCCGTCGGGGCATGAGGGCGAGAGCACGGCGGGGGGGGCGGCCAGAC TCATTGTTGTGGGGGGGGCCCGTCGGGGCATGGGGGCGAGAGCACGGCGGGGGGGGCGGCCAGAC A G MLLT6 Ensembl:ENSG00000275023 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,total RNA Untreated chr17:38705201..38705779;chr17:38705212..38705475 26863196 MeRIP-seq:(Medium) rs1337475840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25278438 108599 RMVar_ID_108599 Human_SNP_ID_623651075 m1A Human chr17 + 38705575 38705575 38705575 CGCGCGGCCCCCCGCTCCCTCCCTCCCCCCTGACCCCCGACCCCCGCCGGCCGGCCCCCCGCCCC CGCGCGGCCCCCCGCTCCCTCCCTCCCCCCTGCCCCCCGACCCCCGCCGGCCGGCCCCCCGCCCC A C MLLT6 Ensembl:ENSG00000275023 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:38705476..38705617 26863410 MeRIP-seq:(Medium) rs906703229 Functional Loss SNV dbSNP153 33..33 33 - - - 108600 RMVar_ID_108600 Human_SNP_ID_623651102 m1A Human chr17 + 38705650 38705650 38705650 GGAGCTCATGGGAGTATGAAGGAGATGGTAGGAGGCTGCTGCGTATGTTCGGACGAGAGGGGCTG GGAGCTCATGGGAGTATGAAGGAGATGGTAGGCGGCTGCTGCGTATGTTCGGACGAGAGGGGCTG A C MLLT6 Ensembl:ENSG00000275023 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38705601..38705802 26863196 MeRIP-seq:(Medium) rs1316233235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820991,Human_RBP_ID_3950476,Human_RBP_ID_4422429,Human_RBP_ID_5577174,Human_RBP_ID_6590014,Human_RBP_ID_8091959,Human_RBP_ID_9377975,Human_RBP_ID_17890988,Human_RBP_ID_18411893 Human_Splice_Rec_1809757,Human_Splice_Rec_1809795,Human_Splice_Rec_1809811 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806 108601 RMVar_ID_108601 Human_SNP_ID_623651253 m1A Human chr17 + 38705995 38705995 38705995 GTTGAGGGAGTTTGGGGAGAGTCTAGGGAGCAATGAGTGAACTCCCCACGCCCCACACCGCGGGT GTTGAGGGAGTTTGGGGAGAGTCTAGGGAGCAGTGAGTGAACTCCCCACGCCCCACACCGCGGGT A G MLLT6 Ensembl:ENSG00000275023 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38705993..38706093 26863196 MeRIP-seq:(Medium) rs929476921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12989386 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806 108602 RMVar_ID_108602 Human_SNP_ID_623651326 m1A Human chr17 + 38706160 38706160 38706160 CCCCCCTCGCTTCCGGATAATGGGAGGAGCGGACTTGGAAAGGGAAGAGAAGGGTCCCAGGGGAG CCCCCCTCGCTTCCGGATAATGGGAGGAGCGGTCTTGGAAAGGGAAGAGAAGGGTCCCAGGGGAG A T MLLT6 Ensembl:ENSG00000275023 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38706158..38706274 26863196 MeRIP-seq:(Medium) rs1379294051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105421,RMVar_hsa_circ_183806 108603 RMVar_ID_108603 Human_SNP_ID_623651728 m1A Human chr17 + 38707554 38707554 38707554 AAGAGGACTGATAATGGAGGTGAGGCGGGCTCATCTGCTGAGGTCAGCAGGGCCCCCTGAGCAGG AAGAGGACTGATAATGGAGGTGAGGCGGGCTCCTCTGCTGAGGTCAGCAGGGCCCCCTGAGCAGG A C MLLT6 Ensembl:ENSG00000275023 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38707542..38707777 26863196 MeRIP-seq:(Medium) rs1279216485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821753,Human_RBP_ID_896452,Human_RBP_ID_5364077,Human_RBP_ID_18988295,Human_RBP_ID_19078858,Human_RBP_ID_22959404,Human_RBP_ID_26333202,Human_RBP_ID_26781596 Human_Splice_Rec_1809760,Human_Splice_Rec_1809798,Human_Splice_Rec_1809814,Human_Splice_Rec_1809828,Human_Splice_Rec_1809832 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806 108604 RMVar_ID_108604 Human_SNP_ID_623652195 m1A Human chr17 + 38709223 38709223 38709223 GAGCAGGGCCGGGAGAGCAAGGCGGCCTCGGGAGCCTGCATGACCTGTAACCGCCATGGATGTCG GAGCAGGGCCGGGAGAGCAAGGCGGCCTCGGGGGCCTGCATGACCTGTAACCGCCATGGATGTCG A G MLLT6 Ensembl:ENSG00000275023 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38709133..38709298 26863196 MeRIP-seq:(Medium) rs373760202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820319,Human_RBP_ID_3952254,Human_RBP_ID_9377979,Human_RBP_ID_18412026,Human_RBP_ID_18988300,Human_RBP_ID_22959405,Human_RBP_ID_26331661,Human_RBP_ID_26812179,Human_RBP_ID_27812596,Human_RBP_ID_27838429 Human_Splice_Rec_1809764,Human_Splice_Rec_1809765,Human_Splice_Rec_1809802,Human_Splice_Rec_1809803,Human_Splice_Rec_1809818,Human_Splice_Rec_1809819,Human_Splice_Rec_1809835 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806,RMVar_hsa_circ_103769,RMVar_hsa_circ_123143,RMVar_hsa_circ_265619,RMVar_hsa_circ_183808,RMVar_hsa_circ_183810,RMVar_hsa_circ_81049,RMVar_hsa_circ_183809 108605 RMVar_ID_108605 Human_SNP_ID_623652288 m1A Human chr17 - 38709504 38709504 38709504 GACGTTGTCCACCTCCAGCACTTCTTCCTCACACAGCAAGCCTGCCATTTGGGCACTAACCAGAG GACGTTGTCCACCTCCAGCACTTCTTCCTCACGCAGCAAGCCTGCCATTTGGGCACTAACCAGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38709157..38712758 32194978 MeRIP-seq:(Medium) rs768492421 Functional Loss SNV dbSNP153 33..33 33 - - - 108606 RMVar_ID_108606 Human_SNP_ID_623652303 m1A Human chr17 - 38709574 38709574 38709574 ACCCGCTCATGCGCTGGTCGCCAGGACTCACCATCTTGCTGAAGTGGTATTTGCAGTAGCCGCAG ACCCGCTCATGCGCTGGTCGCCAGGACTCACCGTCTTGCTGAAGTGGTATTTGCAGTAGCCGCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38709526..38709575 26863196 MeRIP-seq:(Medium) rs1478282842 Functional Loss SNV dbSNP153 33..33 33 - - - 108607 RMVar_ID_108607 Human_SNP_ID_623653977 m1A Human chr17 - 38715774 38715771 38715774 AGAGGAGGAGGAAGAGGAGGAGGAAGAAGAGGAGGCGGAGGTAAAACTGCTCACACCTTTCCCAC AGAGGAGGAGGAAGAGGAGGAGGAAGAAGAGG___CGGAGGTAAAACTGCTCACACCTTTCCCAC GCCT G AC006449.3 Ensembl:ENSG00000275665 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:38715590..38716705;chr17:38715566..38716715 26863196 MeRIP-seq:(Medium) rs777820414 Functional Loss DEL dbSNP153 33..35 33 - - - 108608 RMVar_ID_108608 Human_SNP_ID_623653981 m1A Human chr17 - 38715774 38715774 38715774 AGAGGAGGAGGAAGAGGAGGAGGAAGAAGAGGAGGCGGAGGTAAAACTGCTCACACCTTTCCCAC AGAGGAGGAGGAAGAGGAGGAGGAAGAAGAGGCGGCGGAGGTAAAACTGCTCACACCTTTCCCAC T G AC006449.3 Ensembl:ENSG00000275665 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:38715590..38716705;chr17:38715566..38716715 26863196 MeRIP-seq:(Medium) rs371701573 Functional Loss SNV dbSNP153 33..33 33 - - - 108609 RMVar_ID_108609 Human_SNP_ID_623654640 m1A Human chr17 - 38717584 38717584 38717584 CACCTGAGTGGTGGAGATAGAAGCAGAAGAGGAGGGGAGGGTGCTGGTGAACGGGGAGCGGCTGA CACCTGAGTGGTGGAGATAGAAGCAGAAGAGGGGGGGAGGGTGCTGGTGAACGGGGAGCGGCTGA T C AC006449.3 Ensembl:ENSG00000275665 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38717472..38717641 26863196 MeRIP-seq:(Medium) rs1243936515 Functional Loss SNV dbSNP153 33..33 33 - - - 108610 RMVar_ID_108610 Human_SNP_ID_623655235 m1A Human chr17 + 38719582 38719573 38719582 GGGGGACCTCCCCTCAGGAGAGTCTGTCTTCCATGTGAGGGAAGGGGCAGCCTGGAGGAGGGGCT GGGGGACCTCCCCTCAGGAGAGTC_________TGTGAGGGAAGGGGCAGCCTGGAGGAGGGGCT CTGTCTTCCA C MLLT6 Ensembl:ENSG00000275023 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38719479..38719585 26863196 MeRIP-seq:(Medium) rs1186574585 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_487972,Human_RBP_ID_3950493,Human_RBP_ID_26330708 Human_Splice_Rec_1809780,Human_Splice_Rec_1809781,Human_Splice_Rec_1809846,Human_Splice_Rec_1809847,Human_Splice_Rec_1809855 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806,RMVar_hsa_circ_265619 108611 RMVar_ID_108611 Human_SNP_ID_623655242 m1A Human chr17 + 38719582 38719582 38719582 GGGGGACCTCCCCTCAGGAGAGTCTGTCTTCCATGTGAGGGAAGGGGCAGCCTGGAGGAGGGGCT GGGGGACCTCCCCTCAGGAGAGTCTGTCTTCCGTGTGAGGGAAGGGGCAGCCTGGAGGAGGGGCT A G MLLT6 Ensembl:ENSG00000275023 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38719479..38719585 26863196 MeRIP-seq:(Medium) rs996058528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_487972,Human_RBP_ID_3950493,Human_RBP_ID_26330708 Human_Splice_Rec_1809780,Human_Splice_Rec_1809781,Human_Splice_Rec_1809846,Human_Splice_Rec_1809847,Human_Splice_Rec_1809855 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806,RMVar_hsa_circ_265619 108612 RMVar_ID_108612 Human_SNP_ID_623655418 m1A Human chr17 + 38719921 38719921 38719921 GTCAACAGTGAGGAGGGGTGGCGCCGGTCGGGACGCCTGCCCTAGGGCCCTAACAGTCACCTTTC GTCAACAGTGAGGAGGGGTGGCGCCGGTCGGGGCGCCTGCCCTAGGGCCCTAACAGTCACCTTTC A G MLLT6 Ensembl:ENSG00000275023 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38719916..38720026 26863196 MeRIP-seq:(Medium) rs756981280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19078877 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806,RMVar_hsa_circ_265619 108613 RMVar_ID_108613 Human_SNP_ID_623655419 m1A Human chr17 + 38719921 38719921 38719921 GTCAACAGTGAGGAGGGGTGGCGCCGGTCGGGACGCCTGCCCTAGGGCCCTAACAGTCACCTTTC GTCAACAGTGAGGAGGGGTGGCGCCGGTCGGGTCGCCTGCCCTAGGGCCCTAACAGTCACCTTTC A T MLLT6 Ensembl:ENSG00000275023 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38719916..38720026 26863196 MeRIP-seq:(Medium) rs756981280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19078877 RMVar_hsa_circ_105421,RMVar_hsa_circ_183806,RMVar_hsa_circ_265619 108614 RMVar_ID_108614 Human_SNP_ID_623657418 m1A Human chr17 - 38726380 38726354 38726380 AGGCAGACAGACACACACACACACACACACACACACACACATGCACGCACACACACACTCACACA AGGCAGACAGACACACACACACACACACACAC__________________________TCACACA AGTGTGTGTGTGCGTGCATGTGTGTGT A lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38726329..38726485 26863196 MeRIP-seq:(Medium) rs1452089768 Functional Loss DEL dbSNP153 33..58 33 - - - 108615 RMVar_ID_108615 Human_SNP_ID_623657432 m1A Human chr17 - 38726380 38726370 38726380 AGGCAGACAGACACACACACACACACACACACACACACACATGCACGCACACACACACTCACACA AGGCAGACAGACACACACACACACACACACAC__________GCACGCACACACACACTCACACA CATGTGTGTGT C lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38726329..38726485 26863196 MeRIP-seq:(Medium) rs1567932688 Functional Loss DEL dbSNP153 33..42 33 - - - 108616 RMVar_ID_108616 Human_SNP_ID_623657452 m1A Human chr17 - 38726380 38726380 38726380 AGGCAGACAGACACACACACACACACACACACACACACACATGCACGCACACACACACTCACACA AGGCAGACAGACACACACACACACACACACACTCACACACATGCACGCACACACACACTCACACA T A lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38726329..38726485 26863196 MeRIP-seq:(Medium) rs1348802190 Functional Loss SNV dbSNP153 33..33 33 - - - 108617 RMVar_ID_108617 Human_SNP_ID_623658026 m1A Human chr17 - 38728438 38728438 38728438 CTGAGGGTGGGAACACACGAAGCTCTGCTCTCATGCGTTTCCAAACTCTGCTTCCGCTCTGCAAA CTGAGGGTGGGAACACACGAAGCTCTGCTCTCTTGCGTTTCCAAACTCTGCTTCCGCTCTGCAAA T A lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:38728241..38728650;chr17:38728301..38728612 26863196 MeRIP-seq:(Medium) rs1370151170 Functional Loss SNV dbSNP153 33..33 33 - - - 108618 RMVar_ID_108618 Human_SNP_ID_623658051 m1A Human chr17 - 38728522 38728519 38728523 GCCTCTATATGCACCCCCACTCACACCTCCTCACTGAGGGTGGGAACACCCAACTCCACATGCTC GCCTCTATATGCACCCCCACTCACACCTCCT____GAGGGTGGGAACACCCAACTCCACATGCTC CAGTG C lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:38728351..38728600;chr17:38728298..38728612 26863196 MeRIP-seq:(Medium) rs1226606793 Functional Loss DEL dbSNP153 32..35 33 - - - 108619 RMVar_ID_108619 Human_SNP_ID_623658052 m1A Human chr17 - 38728522 38728522 38728522 GCCTCTATATGCACCCCCACTCACACCTCCTCACTGAGGGTGGGAACACCCAACTCCACATGCTC GCCTCTATATGCACCCCCACTCACACCTCCTCGCTGAGGGTGGGAACACCCAACTCCACATGCTC T C lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:38728351..38728600;chr17:38728298..38728612 26863196 MeRIP-seq:(Medium) rs930790648 Functional Loss SNV dbSNP153 33..33 33 - - - 108620 RMVar_ID_108620 Human_SNP_ID_623658198 m1A Human chr17 - 38729129 38729129 38729129 CTTTGAAAACCTGTCTTCATTTCCAATTTGGGAGAGAGAAGCGTGGAGGTTACCCTTTCTCGGAG CTTTGAAAACCTGTCTTCATTTCCAATTTGGGGGAGAGAAGCGTGGAGGTTACCCTTTCTCGGAG T C lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38728954..38729205 32194978 MeRIP-seq:(Medium) rs753986914 Functional Loss SNV dbSNP153 33..33 33 - - - 108621 RMVar_ID_108621 Human_SNP_ID_623658293 m1A Human chr17 + 38729571 38729571 38729571 TCCATGTAGCAGACCCTTCCTAGGGAGCAGGGAGGGGAAGCCACAGATTGCAAACCCAGGGGCTC TCCATGTAGCAGACCCTTCCTAGGGAGCAGGGGGGGGAAGCCACAGATTGCAAACCCAGGGGCTC A G MLLT6 Ensembl:ENSG00000275023 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38729403..38729653 32194978 MeRIP-seq:(Medium) rs15083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768772,Human_RBP_ID_23723729 RMVar_hsa_circ_265619 108622 RMVar_ID_108622 Human_SNP_ID_623658856 m1A Human chr17 + 38731374 38731374 38731374 CAGCCAGGTCCGTGGTGGCCCTGAAGACCCCCATCAAGGTGGAGCTGGTGGCAGGGAAAACCTAC CAGCCAGGTCCGTGGTGGCCCTGAAGACCCCCGTCAAGGTGGAGCTGGTGGCAGGGAAAACCTAC A G CISD3 Ensembl:ENSG00000277972 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38731301..38731450 26863196 MeRIP-seq:(Medium) rs1017154829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464488,Human_RBP_ID_17654132,Human_RBP_ID_26449781 Human_Splice_Rec_1809882,Human_Splice_Rec_1809883,Human_Splice_Rec_1809886,Human_Splice_Rec_1809887,Human_Splice_Rec_1809889 108623 RMVar_ID_108623 Human_SNP_ID_623659562 m1A Human chr17 + 38733995 38733995 38733995 TCACAGGACCTCAGACACAGGACAAGGTGCAAACACAGACAAGCCCATCAGGGGGCTCCCAACCC TCACAGGACCTCAGACACAGGACAAGGTGCAAGCACAGACAAGCCCATCAGGGGGCTCCCAACCC A G CISD3 Ensembl:ENSG00000277972 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38733945..38734452 32194978 MeRIP-seq:(Medium) rs76161689 Functional Loss SNV dbSNP153 33..33 33 - - - 108624 RMVar_ID_108624 Human_SNP_ID_623659768 m1A Human chr17 + 38734772 38734769 38734773 GGAGAGAAACGGGGAGAGAAAGAAACGATTCTAACTGACTCCTATATGCAGCCAGTTGGAATCAT GGAGAGAAACGGGGAGAGAAAGAAACGATT____CTGACTCCTATATGCAGCCAGTTGGAATCAT TCTAA T CISD3 Ensembl:ENSG00000277972 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38734747..38734847 32194978 MeRIP-seq:(Medium) rs1266357512 Functional Loss DEL dbSNP153 31..34 33 - - - 108625 RMVar_ID_108625 Human_SNP_ID_623659769 m1A Human chr17 + 38734772 38734772 38734772 GGAGAGAAACGGGGAGAGAAAGAAACGATTCTAACTGACTCCTATATGCAGCCAGTTGGAATCAT GGAGAGAAACGGGGAGAGAAAGAAACGATTCTGACTGACTCCTATATGCAGCCAGTTGGAATCAT A G CISD3 Ensembl:ENSG00000277972 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38734747..38734847 32194978 MeRIP-seq:(Medium) rs866258491 Functional Loss SNV dbSNP153 33..33 33 - - - 108626 RMVar_ID_108626 Human_SNP_ID_623659886 m1A Human chr17 + 38735200 38735200 38735200 AAAAAGTGGAAGGAGTGGAGAGGCTTGGCTGGAAGAAGGGAGAGGGTCCCTGGCCTCAAGTTAAG AAAAAGTGGAAGGAGTGGAGAGGCTTGGCTGGGAGAAGGGAGAGGGTCCCTGGCCTCAAGTTAAG A G CISD3 Ensembl:ENSG00000277972 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38735082..38735299 26863196 MeRIP-seq:(Medium) rs962245366 Functional Loss SNV dbSNP153 33..33 33 - - - 108627 RMVar_ID_108627 Human_SNP_ID_623660244 m1A Human chr17 - 38736122 38736122 38736122 AGGACGAGCCACTGAAGGAATACTACACCCTCATGGACATCGCCTACATCTACCCCTGGCGGCGG AGGACGAGCCACTGAAGGAATACTACACCCTCGTGGACATCGCCTACATCTACCCCTGGCGGCGG T C PCGF2 Ensembl:ENSG00000277258 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38735330..38739125 26863196 MeRIP-seq:(Medium) rs1292047416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488076,Human_RBP_ID_896463,Human_RBP_ID_1532794,Human_RBP_ID_1856687,Human_RBP_ID_3521682,Human_RBP_ID_5129550,Human_RBP_ID_9375782,Human_RBP_ID_17259400,Human_RBP_ID_17375312,Human_RBP_ID_17490804,Human_RBP_ID_18291691,Human_RBP_ID_18530601,Human_RBP_ID_18991087,Human_RBP_ID_24372607,Human_RBP_ID_26812185 Human_Splice_Rec_1809906,Human_Splice_Rec_1809907,Human_Splice_Rec_1809926,Human_Splice_Rec_1809927,Human_Splice_Rec_1809944,Human_Splice_Rec_1809945,Human_Splice_Rec_1809964,Human_Splice_Rec_1809965,Human_Splice_Rec_1809982,Human_Splice_Rec_1809983,Human_Splice_Rec_1809998,Human_Splice_Rec_1809999 RMVar_hsa_circ_268490 108628 RMVar_ID_108628 Human_SNP_ID_623661125 m1A Human chr17 - 38738792 38738792 38738792 GGAGCAGGAGAAGGGGGCTCTGAGTGATGATGAGATTGTCAGCCTCTCCATCGAATTCTACGAAG GGAGCAGGAGAAGGGGGCTCTGAGTGATGATGTGATTGTCAGCCTCTCCATCGAATTCTACGAAG T A PCGF2 Ensembl:ENSG00000277258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38735183..38738875 26863196 MeRIP-seq:(Medium) rs752773081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488082,Human_RBP_ID_1181609,Human_RBP_ID_1532796,Human_RBP_ID_1856690,Human_RBP_ID_3521684,Human_RBP_ID_23723786 Human_Splice_Rec_1809902,Human_Splice_Rec_1809922,Human_Splice_Rec_1809940,Human_Splice_Rec_1809958,Human_Splice_Rec_1809959,Human_Splice_Rec_1809976,Human_Splice_Rec_1809977,Human_Splice_Rec_1809992,Human_Splice_Rec_1809993 RMVar_hsa_circ_4026,RMVar_hsa_circ_268490 108629 RMVar_ID_108629 Human_SNP_ID_623661682 m1A Human chr17 + 38740397 38740397 38740397 TTCAGCTCTGTGATTTTGATCCGTGTAGTCCGATGCATGATTCCGGGGTCGGGGGTGGGGGGACT TTCAGCTCTGTGATTTTGATCCGTGTAGTCCGGTGCATGATTCCGGGGTCGGGGGTGGGGGGACT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:38740261..38740505 26863196 MeRIP-seq:(Medium) rs1424643045 Functional Loss SNV dbSNP153 33..33 33 - - - 108630 RMVar_ID_108630 Human_SNP_ID_623661716 m1A Human chr17 - 38740439 38740439 38740439 GGGTTTCTGATTCCACTTCCGTTTCCCAGGGCAACGCTCCCCAGTCCCCCCACCCCCGACCCCGG GGGTTTCTGATTCCACTTCCGTTTCCCAGGGCGACGCTCCCCAGTCCCCCCACCCCCGACCCCGG T C PCGF2 Ensembl:ENSG00000277258 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:38740311..38746485 26863410 MeRIP-seq:(Medium) rs748666781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129153,Human_RBP_ID_17080619,Human_RBP_ID_18943095 Human_Splice_Rec_1809894,Human_Splice_Rec_1809914,Human_Splice_Rec_1809932,Human_Splice_Rec_1809950,Human_Splice_Rec_1809968 RMVar_hsa_circ_4026,RMVar_hsa_circ_268490 108631 RMVar_ID_108631 Human_SNP_ID_623663181 m1A Human chr17 + 38746319 38746319 38746319 AAGGCCAGATAGACACGCCACAACCCTCCCCCACCCTGCGCCACACACACACACAATCACAGCCA AAGGCCAGATAGACACGCCACAACCCTCCCCCCCCCTGCGCCACACACACACACAATCACAGCCA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:38746268..38746422 26863196 MeRIP-seq:(Medium) rs1390989195 Functional Loss SNV dbSNP153 33..33 33 - - - 108632 RMVar_ID_108632 Human_SNP_ID_623663601 m1A Human chr17 + 38748075 38748075 38748075 AGGGACTGACGGGGCGCGGGGGGTGCGAAGGCAGGATCGGCTCAGAGCCTCCCCCTCCCATCGGG AGGGACTGACGGGGCGCGGGGGGTGCGAAGGCGGGATCGGCTCAGAGCCTCCCCCTCCCATCGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38748066..38748178 26863196 MeRIP-seq:(Medium) rs542720972 Functional Loss SNV dbSNP153 33..33 33 - - - 108633 RMVar_ID_108633 Human_SNP_ID_623663653 m1A Human chr17 + 38748250 38748241 38748250 CTCGGGGAGGGGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCT CTCGGGGAGGGGGGGATGGGAGGG_________AGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCT GAGGGAGGGA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:38748176..38748300 26863410 MeRIP-seq:(Medium) rs1010905506 Functional Loss DEL dbSNP153 25..33 33 - - - 108634 RMVar_ID_108634 Human_SNP_ID_623663655 m1A Human chr17 + 38748246 38748246 38748246 GGGTCTCGGGGAGGGGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGT GGGTCTCGGGGAGGGGGGGATGGGAGGGAGGGGGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:38748142..38748358;chr17:38748122..38748343 26863196,32194978 MeRIP-seq:(Medium) rs1199227481 Functional Loss SNV dbSNP153 33..33 33 - - - 108635 RMVar_ID_108635 Human_SNP_ID_623663657 m1A Human chr17 + 38748250 38748250 38748250 CTCGGGGAGGGGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCT CTCGGGGAGGGGGGGATGGGAGGGAGGGAGGGGAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:38748176..38748300 26863410 MeRIP-seq:(Medium) rs1214687574 Functional Loss SNV dbSNP153 33..33 33 - - - 108636 RMVar_ID_108636 Human_SNP_ID_623663658 m1A Human chr17 + 38748251 38748251 38748251 TCGGGGAGGGGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCTC TCGGGGAGGGGGGGATGGGAGGGAGGGAGGGAGGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:38748228..38748361 26863196 MeRIP-seq:(Medium) rs980652966 Functional Loss SNV dbSNP153 33..33 33 - - - 108637 RMVar_ID_108637 Human_SNP_ID_623663662 m1A Human chr17 + 38748260 38748260 38748260 GGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCTCGCCCGGGCG GGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGGGGGGGGCCGCAGCCGTGTCGCTCGCCCGGGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38748215..38748341 26863196 MeRIP-seq:(Medium) rs941971677 Functional Loss SNV dbSNP153 33..33 33 - - - 108638 RMVar_ID_108638 Human_SNP_ID_623663663 m1A Human chr17 + 38748260 38748260 38748260 GGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGAGGGGGGCCGCAGCCGTGTCGCTCGCCCGGGCG GGGGGATGGGAGGGAGGGAGGGAAGGGAGGGGTGGGGGGCCGCAGCCGTGTCGCTCGCCCGGGCG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38748215..38748341 26863196 MeRIP-seq:(Medium) rs941971677 Functional Loss SNV dbSNP153 33..33 33 - - - 108639 RMVar_ID_108639 Human_SNP_ID_623663681 m1A Human chr17 + 38748320 38748320 38748320 GGGCGGCGGGAGGGGAGAAACCTACGGTAAGAAAGGAGTTTGTGAAAGCGGCTTGGGGTGGGAGG GGGCGGCGGGAGGGGAGAAACCTACGGTAAGAGAGGAGTTTGTGAAAGCGGCTTGGGGTGGGAGG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:38748225..38748339 26863410 MeRIP-seq:(Medium) rs1187877485 Functional Loss SNV dbSNP153 33..33 33 - - - 108640 RMVar_ID_108640 Human_SNP_ID_623663911 m1A Human chr17 + 38749090 38749087 38749090 GGAGGCTGCGCCCCCGGCGTGCTCGGGCAGAGAAGAACGGAGGCCCGCTGAGGATGGGAACTCAG GGAGGCTGCGCCCCCGGCGTGCTCGGGCAG___AGAACGGAGGCCCGCTGAGGATGGGAACTCAG GAGA G LOC100287808 RNACentral:URS0000BC4454 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38749080..38749154 26863196 MeRIP-seq:(Medium) rs1385726032 Functional Loss DEL dbSNP153 31..33 33 - - - 108641 RMVar_ID_108641 Human_SNP_ID_623665045 m1A Human chr17 - 38752801 38752801 38752801 TCACCATGATTGCGGTGTACTAGGATCCCTCGATCGCCAGAGCAATTCCAGTAAACCGGGTCTAG TCACCATGATTGCGGTGTACTAGGATCCCTCGGTCGCCAGAGCAATTCCAGTAAACCGGGTCTAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38752751..38752881 26863196 MeRIP-seq:(Medium) rs779999849 Functional Loss SNV dbSNP153 33..33 33 - - - 108642 RMVar_ID_108642 Human_SNP_ID_623665046 m1A Human chr17 - 38752801 38752801 38752801 TCACCATGATTGCGGTGTACTAGGATCCCTCGATCGCCAGAGCAATTCCAGTAAACCGGGTCTAG TCACCATGATTGCGGTGTACTAGGATCCCTCGCTCGCCAGAGCAATTCCAGTAAACCGGGTCTAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38752751..38752881 26863196 MeRIP-seq:(Medium) rs779999849 Functional Loss SNV dbSNP153 33..33 33 - - - 108643 RMVar_ID_108643 Human_SNP_ID_623665053 m1A Human chr17 - 38752812 38752807 38752813 AACTCCCCATCTCACCATGATTGCGGTGTACTAGGATCCCTCGATCGCCAGAGCAATTCCAGTAA AACTCCCCATCTCACCATGATTGCGGTGTAC______CCCTCGATCGCCAGAGCAATTCCAGTAA GATCCTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:38752751..38752882;chr17:38752751..38752825 26863196 MeRIP-seq:(Medium) rs1567641859 Functional Loss DEL dbSNP153 32..37 33 - - - 108644 RMVar_ID_108644 Human_SNP_ID_623665058 m1A Human chr17 - 38752812 38752812 38752812 AACTCCCCATCTCACCATGATTGCGGTGTACTAGGATCCCTCGATCGCCAGAGCAATTCCAGTAA AACTCCCCATCTCACCATGATTGCGGTGTACTCGGATCCCTCGATCGCCAGAGCAATTCCAGTAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:38752751..38752882;chr17:38752751..38752825 26863196 MeRIP-seq:(Medium) rs770748025 Functional Loss SNV dbSNP153 33..33 33 - - - 108645 RMVar_ID_108645 Human_SNP_ID_623665064 m1A Human chr17 + 38752827 38752827 38752827 TGGCGATCGAGGGATCCTAGTACACCGCAATCATGGTGAGATGGGGAGTTAAAGCAAAGGGGCAT TGGCGATCGAGGGATCCTAGTACACCGCAATCGTGGTGAGATGGGGAGTTAAAGCAAAGGGGCAT A G PSMB3 Ensembl:ENSG00000277791 Protein coding start codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38752776..38752850 32194978 MeRIP-seq:(Medium) rs1275272038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465324,Human_RBP_ID_5467541,Human_RBP_ID_9326587,Human_RBP_ID_23210317,Human_RBP_ID_27664586 Human_Splice_Rec_1810001,Human_Splice_Rec_1810017,Human_Splice_Rec_1810027 RMVar_hsa_circ_88325,RMVar_hsa_circ_110436,RMVar_hsa_circ_183817,RMVar_hsa_circ_183818 108646 RMVar_ID_108646 Human_SNP_ID_623665201 m1A Human chr17 + 38753246 38753246 38753246 CTGCAGACAGGCGCTTCGGGATCCAGGCCCAGATGGTGACCACGGACTTCCAGAAGATCTTTCCC CTGCAGACAGGCGCTTCGGGATCCAGGCCCAGTTGGTGACCACGGACTTCCAGAAGATCTTTCCC A T PSMB3 Ensembl:ENSG00000277791 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38753196..38753271 26863196 MeRIP-seq:(Medium) rs4907 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_488098,Human_RBP_ID_1532812,Human_RBP_ID_1856698,Human_RBP_ID_4422803,Human_RBP_ID_12989714,Human_RBP_ID_18696176 Human_Splice_Rec_1810002,Human_Splice_Rec_1810003,Human_Splice_Rec_1810012,Human_Splice_Rec_1810013,Human_Splice_Rec_1810018,Human_Splice_Rec_1810019,Human_Splice_Rec_1810028,Human_Splice_Rec_1810029 RMVar_hsa_circ_88325,RMVar_hsa_circ_110436,RMVar_hsa_circ_183817,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819 108647 RMVar_ID_108647 Human_SNP_ID_623668140 m1A Human chr17 - 38764103 38764103 38764103 TGATTTTGTCCTTCTCGCTGCAGAGGGAGAAAATCACAAGAAAACATCTCTACCCATCTGGACCG TGATTTTGTCCTTCTCGCTGCAGAGGGAGAAACTCACAAGAAAACATCTCTACCCATCTGGACCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38764101..38764225 32194978 MeRIP-seq:(Medium) rs1358632305 Functional Loss SNV dbSNP153 33..33 33 - - - 108648 RMVar_ID_108648 Human_SNP_ID_623669699 m1A Human chr17 + 38770884 38770884 38770884 GGTTCAGGTGGTGACCCTGGATGGGAATCTGGAGGCAGAAAGAGGTCAAAGGCAGCAATGAATGA GGTTCAGGTGGTGACCCTGGATGGGAATCTGGCGGCAGAAAGAGGTCAAAGGCAGCAATGAATGA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38770876..38771050 26863196 MeRIP-seq:(Medium) rs1243486866 Functional Loss SNV dbSNP153 33..33 33 - - - 108649 RMVar_ID_108649 Human_SNP_ID_623671393 m1A Human chr17 - 38777638 38777638 38777638 ATTTTCACCTGCAAGGCTCCTTCTGTACCTAGAGTAGGCGCCTCTTAAACCTTAAGAAGAATGGA ATTTTCACCTGCAAGGCTCCTTCTGTACCTAGGGTAGGCGCCTCTTAAACCTTAAGAAGAATGGA T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38777636..38777750 26863196 MeRIP-seq:(Medium) rs951367695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78353,RMVar_hsa_circ_183827,RMVar_hsa_circ_95216,RMVar_hsa_circ_83691,RMVar_hsa_circ_47143,RMVar_hsa_circ_99057,RMVar_hsa_circ_183830,RMVar_hsa_circ_112256,RMVar_hsa_circ_183831,RMVar_hsa_circ_183832,RMVar_hsa_circ_183833 108650 RMVar_ID_108650 Human_SNP_ID_623676983 m1A Human chr17 - 38799409 38799409 38799409 CCGCCGCCGCCCCGGGCATGTCGTCCAACTGCACCAGCACCACGGCGGTGGCGGTGGCGCCGCTC CCGCCGCCGCCCCGGGCATGTCGTCCAACTGCGCCAGCACCACGGCGGTGGCGGTGGCGCCGCTC T C PIP4K2B Ensembl:ENSG00000276293 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:38799357..38799485 26863196 MeRIP-seq:(Medium) rs1359841722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465326,Human_RBP_ID_9327271,Human_RBP_ID_9375795 108651 RMVar_ID_108651 Human_SNP_ID_623677014 m1A Human chr17 + 38799450 38799449 38799451 ACGACATGCCCGGGGCGGCGGCGGCGGCGGCGAAAGAGGGGGGCGGCGGAGACAGCGCACAAGCC ACGACATGCCCGGGGCGGCGGCGGCGGCGGCG__AGAGGGGGGCGGCGGAGACAGCGCACAAGCC GAA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:38799361..38799460 26863410 MeRIP-seq:(Medium) rs1567666316 Functional Loss DEL dbSNP153 33..34 33 - - - 108652 RMVar_ID_108652 Human_SNP_ID_623677075 m1A Human chr17 - 38799603 38799584 38799604 GCGGGCCGGCGGGCTCCCCGGGGCGGGGCGGGAGGGCGGGGCGTGGGGCGGACGGAACCACCGGG GCGGGCCGGCGGGCTCCCCGGGGCGGGGCGG____________________ACGGAACCACCGGG TCCGCCCCACGCCCCGCCCTC T PIP4K2B Ensembl:ENSG00000276293 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:38799511..38799611 26863410 MeRIP-seq:(Medium) rs1291090857 Functional Loss DEL dbSNP153 32..51 33 - - - 108653 RMVar_ID_108653 Human_SNP_ID_623677086 m1A Human chr17 - 38799603 38799603 38799603 GCGGGCCGGCGGGCTCCCCGGGGCGGGGCGGGAGGGCGGGGCGTGGGGCGGACGGAACCACCGGG GCGGGCCGGCGGGCTCCCCGGGGCGGGGCGGGGGGGCGGGGCGTGGGGCGGACGGAACCACCGGG T C PIP4K2B Ensembl:ENSG00000276293 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:38799511..38799611 26863410 MeRIP-seq:(Medium) rs894087549 Functional Loss SNV dbSNP153 33..33 33 - - - 108654 RMVar_ID_108654 Human_SNP_ID_623677188 m1A Human chr17 + 38799822 38799822 38799822 TCGGGGCCCCGTGCCGGAGCCGGAAGGGGAGGAGGGCTGGGCAGGCGTCGCTGTGGACCGCGGGA TCGGGGCCCCGTGCCGGAGCCGGAAGGGGAGGGGGGCTGGGCAGGCGTCGCTGTGGACCGCGGGA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:38799734..38799860 26863410 MeRIP-seq:(Medium) rs1160590705 Functional Loss SNV dbSNP153 33..33 33 - - - 108655 RMVar_ID_108655 Human_SNP_ID_623680104 m1A Human chr17 - 38810520 38810520 38810520 AGAAGAAAAAGAAGCACAAGAAACATAAGCACAGAAGCTCGAGTAGTGATCGTTCCAGCAGCGAG AGAAGAAAAAGAAGCACAAGAAACATAAGCACGGAAGCTCGAGTAGTGATCGTTCCAGCAGCGAG T C CWC25 Ensembl:ENSG00000273559 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38810470..38812858 26863196 MeRIP-seq:(Medium) rs1224568506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51061,Human_RBP_ID_24544848 Human_Splice_Rec_1810096,Human_Splice_Rec_1810097,Human_Splice_Rec_1810116,Human_Splice_Rec_1810117,Human_Splice_Rec_1810132,Human_Splice_Rec_1810141,Human_Splice_Rec_1810160,Human_Splice_Rec_1810174 RMVar_hsa_circ_21482 108656 RMVar_ID_108656 Human_SNP_ID_623681409 m1A Human chr17 - 38815068 38815068 38815068 CAGGAAAAAAGAAGAAAAGTTGGACTGGATGTACCAGGGTCCTGGTGGGATGGTGAACCGTGACG CAGGAAAAAAGAAGAAAAGTTGGACTGGATGTTCCAGGGTCCTGGTGGGATGGTGAACCGTGACG T A CWC25 Ensembl:ENSG00000273559 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38814976..38825303 26863196 MeRIP-seq:(Medium) rs767935154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_51063,Human_RBP_ID_897538,Human_RBP_ID_1532856,Human_RBP_ID_3950503,Human_RBP_ID_5364110,Human_RBP_ID_8232362,Human_RBP_ID_9346255,Human_RBP_ID_9375799,Human_RBP_ID_17891108,Human_RBP_ID_18988315,Human_RBP_ID_21976136,Human_RBP_ID_22061265,Human_RBP_ID_22445415,Human_RBP_ID_22656191,Human_RBP_ID_24544850,Human_RBP_ID_26331676,Human_RBP_ID_27812611 Human_Splice_Rec_1810092,Human_Splice_Rec_1810112,Human_Splice_Rec_1810128,Human_Splice_Rec_1810156,Human_Splice_Rec_1810170 RMVar_hsa_circ_2012,RMVar_hsa_circ_21482,RMVar_hsa_circ_71196,RMVar_hsa_circ_183841,RMVar_hsa_circ_339037 108657 RMVar_ID_108657 Human_SNP_ID_623691372 m1A Human chr17 - 38849586 38849586 38849586 GGCACCTGTAATCCCAACACTTTCGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCAAGA GGCACCTGTAATCCCAACACTTTCGGAGGCCAGGGCAGGCAGATCATGAGGTCAGGAGTTCAAGA T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1463545963 Functional Loss SNV dbSNP153 33..33 33 - - - 108658 RMVar_ID_108658 Human_SNP_ID_623692359 m1A Human chr17 + 38852996 38852996 38852996 CCACAGGCCCATTGAGTGCTTTTAAAAGGGGGAGTATAGCAACGTGCAAAGACCTCACCTGTGTT CCACAGGCCCATTGAGTGCTTTTAAAAGGGGGGGTATAGCAACGTGCAAAGACCTCACCTGTGTT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:38852990..38853133 26863196 MeRIP-seq:(Medium) rs1021913440 Functional Loss SNV dbSNP153 33..33 33 - - - 108659 RMVar_ID_108659 Human_SNP_ID_623692385 m1A Human chr17 - 38853080 38853080 38853080 TCCACAGGACGTGGTGGGTCCTCTGGTGCGAAATTCCGGATTTCCTTGGGTCTTCCGGTAGGAGC TCCACAGGACGTGGTGGGTCCTCTGGTGCGAAGTTCCGGATTTCCTTGGGTCTTCCGGTAGGAGC T C RPL23 Ensembl:ENSG00000125691 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:38853001..38853150 26863410 MeRIP-seq:(Medium) rs1471822692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47775,Human_RBP_ID_488232,Human_RBP_ID_765132,Human_RBP_ID_1007733,Human_RBP_ID_1181627,Human_RBP_ID_1286107,Human_RBP_ID_1532885,Human_RBP_ID_1856819,Human_RBP_ID_2505056,Human_RBP_ID_3521784,Human_RBP_ID_4471950,Human_RBP_ID_6590418,Human_RBP_ID_8451202,Human_RBP_ID_9071682,Human_RBP_ID_12990780,Human_RBP_ID_17259422,Human_RBP_ID_17375338,Human_RBP_ID_17490824,Human_RBP_ID_17653810,Human_RBP_ID_17691902,Human_RBP_ID_17904821,Human_RBP_ID_18164478,Human_RBP_ID_18438853,Human_RBP_ID_18696276,Human_RBP_ID_22442897,Human_RBP_ID_23209923,Human_RBP_ID_23724008,Human_RBP_ID_24415186,Human_RBP_ID_25341574,Human_RBP_ID_26460482 Human_Splice_Rec_1810178,Human_Splice_Rec_1810179,Human_Splice_Rec_1810186,Human_Splice_Rec_1810187,Human_Splice_Rec_1810196,Human_Splice_Rec_1810197,Human_Splice_Rec_1810204,Human_Splice_Rec_1810205,Human_Splice_Rec_1810212,Human_Splice_Rec_1810213,Human_Splice_Rec_1810216,Human_Splice_Rec_1810217,Human_Splice_Rec_1810222,Human_Splice_Rec_1810223,Human_Splice_Rec_1810228,Human_Splice_Rec_1810229,Human_Splice_Rec_1810234 Human_miRNA_ID_3058075 RMVar_hsa_circ_103813,RMVar_hsa_circ_49615,RMVar_hsa_circ_183846 108660 RMVar_ID_108660 Human_SNP_ID_623692576 m1A Human chr17 + 38853628 38853628 38853628 AGGAGAGCAAAGCGCCCCAGCTGCCTAGGGCCACCGCTCCTGACGAATCCGCCAGCCACTGCACG AGGAGAGCAAAGCGCCCCAGCTGCCTAGGGCCCCCGCTCCTGACGAATCCGCCAGCCACTGCACG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr17:38853626..38853750;chr17:38853624..38853775 26863410,26863196 MeRIP-seq:(Medium) rs953095726 Functional Loss SNV dbSNP153 33..33 33 - - - 108661 RMVar_ID_108661 Human_SNP_ID_623692577 m1A Human chr17 + 38853628 38853628 38853628 AGGAGAGCAAAGCGCCCCAGCTGCCTAGGGCCACCGCTCCTGACGAATCCGCCAGCCACTGCACG AGGAGAGCAAAGCGCCCCAGCTGCCTAGGGCCGCCGCTCCTGACGAATCCGCCAGCCACTGCACG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr17:38853626..38853750;chr17:38853624..38853775 26863410,26863196 MeRIP-seq:(Medium) rs953095726 Functional Loss SNV dbSNP153 33..33 33 - - - 108662 RMVar_ID_108662 Human_SNP_ID_623692606 m1A Human chr17 - 38853699 38853699 38853699 TTCTTTTTTCCGGCGTTCAAGATGTCGAAGCGAGGTGAGGTTTTGTTTCTGGAGGATCCTCCACC TTCTTTTTTCCGGCGTTCAAGATGTCGAAGCGGGGTGAGGTTTTGTTTCTGGAGGATCCTCCACC T C RPL23 Ensembl:ENSG00000125691 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:38853676..38853725 26863196 MeRIP-seq:(Medium) rs531763616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237764,Human_RBP_ID_488234,Human_RBP_ID_768415,Human_RBP_ID_1532889,Human_RBP_ID_1856822,Human_RBP_ID_4423106,Human_RBP_ID_12990810,Human_RBP_ID_17654154,Human_RBP_ID_17904824,Human_RBP_ID_22212975,Human_RBP_ID_22807898,Human_RBP_ID_23169019,Human_RBP_ID_24415187,Human_RBP_ID_24481882,Human_RBP_ID_26460483 Human_Splice_Rec_1810177,Human_Splice_Rec_1810185,Human_Splice_Rec_1810195,Human_Splice_Rec_1810211,Human_Splice_Rec_1810215,Human_Splice_Rec_1810233 108663 RMVar_ID_108663 Human_SNP_ID_623694934 m1A Human chr17 - 38861699 38861699 38861699 ATTTGACTGCAGATCAAGAAGTCCCCGGTTCAAATCCGGGTGCCCCCTCACAGCCACCGTTTTAA ATTTGACTGCAGATCAAGAAGTCCCCGGTTCACATCCGGGTGCCCCCTCACAGCCACCGTTTTAA T G tRNA-Cys-GCA-14-1 RNACentral:URS0000646601 tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs1047311503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488236,Human_RBP_ID_1181630,Human_RBP_ID_1238675,Human_RBP_ID_1532895,Human_RBP_ID_1856827,Human_RBP_ID_3521788,Human_RBP_ID_4471957,Human_RBP_ID_5275071,Human_RBP_ID_5496947,Human_RBP_ID_5536108,Human_RBP_ID_8253378,Human_RBP_ID_8451210,Human_RBP_ID_9071687,Human_RBP_ID_9885592,Human_RBP_ID_13228836,Human_RBP_ID_17380448,Human_RBP_ID_17582794,Human_RBP_ID_17891146,Human_RBP_ID_18696285,Human_RBP_ID_20208999,Human_RBP_ID_22804214,Human_RBP_ID_22960744,Human_RBP_ID_23129179,Human_RBP_ID_23169021,Human_RBP_ID_24417527,Human_RBP_ID_24478793,Human_RBP_ID_25341579,Human_RBP_ID_26959848,Human_RBP_ID_27253265,Human_RBP_ID_27451558 108664 RMVar_ID_108664 Human_SNP_ID_623696895 m1A Human chr17 + 38867700 38867700 38867700 CATTTGACTGCAGATCAAGAGGTCCCCGGTTCAAATCCGGGTGCCCCCTCGGGTTTCTTTAAGTT CATTTGACTGCAGATCAAGAGGTCCCCGGTTCGAATCCGGGTGCCCCCTCGGGTTTCTTTAAGTT A G tRNA-Cys-GCA-2-2 RNACentral:URS0000417A0F tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs931559368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238677,Human_RBP_ID_1532897,Human_RBP_ID_1856829,Human_RBP_ID_3521791,Human_RBP_ID_5260061,Human_RBP_ID_5274914,Human_RBP_ID_6590435,Human_RBP_ID_8253380,Human_RBP_ID_8451215,Human_RBP_ID_9859137,Human_RBP_ID_17891150,Human_RBP_ID_18696290,Human_RBP_ID_20209003,Human_RBP_ID_22212984,Human_RBP_ID_22804216,Human_RBP_ID_23129186,Human_RBP_ID_23169022,Human_RBP_ID_25278940,Human_RBP_ID_26959850,Human_RBP_ID_27451559 108665 RMVar_ID_108665 Human_SNP_ID_623697946 m1A Human chr17 + 38870444 38870444 38870444 ATCCCAGTCTGAAAACCAGGAGATCTGGGGCGAGGCGGGAAGTCCACGCGTAGCGGGCAGCCGCT ATCCCAGTCTGAAAACCAGGAGATCTGGGGCGCGGCGGGAAGTCCACGCGTAGCGGGCAGCCGCT A C LASP1 Ensembl:ENSG00000002834 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38870441..38870575 26863196 MeRIP-seq:(Medium) rs1299095492 Functional Loss SNV dbSNP153 33..33 33 - - - 108666 RMVar_ID_108666 Human_SNP_ID_623701946 m1A Human chr17 + 38886686 38886685 38886687 GACCGTCTGGTGGGTGTAGGGTGAGCAGAGGGACACAGTGTGGGGTGCAGGGGGTGTGTGGACAT GACCGTCTGGTGGGTGTAGGGTGAGCAGAGGG__ACAGTGTGGGGTGCAGGGGGTGTGTGGACAT GAC G LASP1 Ensembl:ENSG00000002834 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:38886684..38886783 26863196 MeRIP-seq:(Medium) rs955441301 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6590447,Human_RBP_ID_20291910,Human_RBP_ID_21974317 RMVar_hsa_circ_183849,RMVar_hsa_circ_316168,RMVar_hsa_circ_374368,RMVar_hsa_circ_127058,RMVar_hsa_circ_183848 108667 RMVar_ID_108667 Human_SNP_ID_623704948 m1A Human chr17 - 38898464 38898464 38898464 TCTTGATTCTCTGGAGCTCGGGCGTGTCTGCCACTACGCTGAAACCTTTGCCCTTGTTCTTCTCA TCTTGATTCTCTGGAGCTCGGGCGTGTCTGCCTCTACGCTGAAACCTTTGCCCTTGTTCTTCTCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38898401..38898545 32194978 MeRIP-seq:(Medium) rs1280405349 Functional Loss SNV dbSNP153 33..33 33 - - - 108668 RMVar_ID_108668 Human_SNP_ID_623708864 m1A Human chr17 + 38914401 38914401 38914401 CGGGGGCGAGGGCATGGAGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCC CGGGGGCGAGGGCATGGAGCCAGAGCGTCGGGTTTCACAGGACGGCAGCAGCTACCGGCGGCCCC A T LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:38914285..38914524;chr17:38914286..38914522 26863196 MeRIP-seq:(Medium) rs61739902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46549,Human_RBP_ID_5185186,Human_RBP_ID_9375805,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_26449900,Human_RBP_ID_27812613 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 108669 RMVar_ID_108669 Human_SNP_ID_623708869 m1A Human chr17 + 38914405 38914405 38914405 GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCCTGGA GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCCCAGGACGGCAGCAGCTACCGGCGGCCCCTGGA A C LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs525989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46549,Human_RBP_ID_5185186,Human_RBP_ID_9375805,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_26449900,Human_RBP_ID_27812614 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 GWAS_ID_15210,GWAS_ID_15211,GWAS_ID_15212,GWAS_ID_15213,GWAS_ID_15214 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 108670 RMVar_ID_108670 Human_SNP_ID_623708870 m1A Human chr17 + 38914405 38914405 38914405 GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCCTGGA GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCGCAGGACGGCAGCAGCTACCGGCGGCCCCTGGA A G LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs525989 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_46549,Human_RBP_ID_5185186,Human_RBP_ID_9375805,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_26449900,Human_RBP_ID_27812614 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 GWAS_ID_15210,GWAS_ID_15211,GWAS_ID_15212,GWAS_ID_15213,GWAS_ID_15214 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 108671 RMVar_ID_108671 Human_SNP_ID_623708871 m1A Human chr17 + 38914405 38914405 38914405 GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCCTGGA GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCTCAGGACGGCAGCAGCTACCGGCGGCCCCTGGA A T LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs525989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46549,Human_RBP_ID_5185186,Human_RBP_ID_9375805,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_26449900,Human_RBP_ID_27812614 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 GWAS_ID_15210,GWAS_ID_15211,GWAS_ID_15212,GWAS_ID_15213,GWAS_ID_15214 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 108672 RMVar_ID_108672 Human_SNP_ID_623708880 m1A Human chr17 + 38914418 38914417 38914419 AGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCCTGGAGCAGCAGCAGCCT AGCCAGAGCGTCGGGATTCACAGGACGGCAGC__CTACCGGCGGCCCCTGGAGCAGCAGCAGCCT CAG C LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:38914283..38915180;chr17:38914275..38914523 26863196 MeRIP-seq:(Medium) rs1567705712 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_904692,Human_RBP_ID_5185186,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_27812614 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 108673 RMVar_ID_108673 Human_SNP_ID_623709146 m1A Human chr17 - 38915101 38915101 38915101 GGGGCGCTGCGCTGTATGGAGACTGGGGCTGCAGGCTCCTTGTAGCCACCATAGGACTGGGCCAC GGGGCGCTGCGCTGTATGGAGACTGGGGCTGCTGGCTCCTTGTAGCCACCATAGGACTGGGCCAC T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38915051..38915150 26863196 MeRIP-seq:(Medium) rs1219225711 Functional Loss SNV dbSNP153 33..33 33 - - - 108674 RMVar_ID_108674 Human_SNP_ID_623709147 m1A Human chr17 - 38915101 38915101 38915101 GGGGCGCTGCGCTGTATGGAGACTGGGGCTGCAGGCTCCTTGTAGCCACCATAGGACTGGGCCAC GGGGCGCTGCGCTGTATGGAGACTGGGGCTGCGGGCTCCTTGTAGCCACCATAGGACTGGGCCAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:38915051..38915150 26863196 MeRIP-seq:(Medium) rs1219225711 Functional Loss SNV dbSNP153 33..33 33 - - - 108675 RMVar_ID_108675 Human_SNP_ID_623709172 m1A Human chr17 - 38915148 38915148 38915148 CTCTGGCCTCTCCCCTCCGGCCAGGGTTACTCACCCCGCCACCACCTGGGGCGCTGCGCTGTATG CTCTGGCCTCTCCCCTCCGGCCAGGGTTACTCCCCCCGCCACCACCTGGGGCGCTGCGCTGTATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:38915101..38915150;chr17:38914994..38915197 26863196 MeRIP-seq:(Medium) rs1413308621 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 108676 RMVar_ID_108676 Human_SNP_ID_623710283 m1A Human chr17 - 38918977 38918977 38918977 TCCATCCAGAGAGAAAACCAAGAAGTCGATCAAGGGGGAAGCCTGCCAGAGGAGGGAGCCCGCAG TCCATCCAGAGAGAAAACCAAGAAGTCGATCACGGGGGAAGCCTGCCAGAGGAGGGAGCCCGCAG T G AC006441.3 Ensembl:ENSG00000265784 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38918926..38919150 26863196 MeRIP-seq:(Medium) rs1063333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8093483 108677 RMVar_ID_108677 Human_SNP_ID_623752769 m1A Human chr17 - 39088886 39088886 39088886 GGAGTGCAGTGGCACAATCTCAGCTGACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTG GGAGTGCAGTGGCACAATCTCAGCTGACTGCACCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTG T G PLXDC1 Ensembl:ENSG00000161381 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:39088881..39088963 26863410 MeRIP-seq:(Medium) rs1382220962 Functional Loss SNV dbSNP153 33..33 33 - - - 108678 RMVar_ID_108678 Human_SNP_ID_623769475 m1A Human chr17 + 39154484 39154484 39154484 CTCCGGAGACCAACAAAACGAGGTAACTCCGGAGCACAGAGGGGGCACCCGGATTTGAACCGGGG CTCCGGAGACCAACAAAACGAGGTAACTCCGGCGCACAGAGGGGGCACCCGGATTTGAACCGGGG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:39154434..39154558 26863196 MeRIP-seq:(Medium) rs1007300123 Functional Loss SNV dbSNP153 33..33 33 - - - 108679 RMVar_ID_108679 Human_SNP_ID_623769476 m1A Human chr17 + 39154484 39154484 39154484 CTCCGGAGACCAACAAAACGAGGTAACTCCGGAGCACAGAGGGGGCACCCGGATTTGAACCGGGG CTCCGGAGACCAACAAAACGAGGTAACTCCGGGGCACAGAGGGGGCACCCGGATTTGAACCGGGG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:39154434..39154558 26863196 MeRIP-seq:(Medium) rs1007300123 Functional Loss SNV dbSNP153 33..33 33 - - - 108680 RMVar_ID_108680 Human_SNP_ID_623769477 m1A Human chr17 + 39154484 39154484 39154484 CTCCGGAGACCAACAAAACGAGGTAACTCCGGAGCACAGAGGGGGCACCCGGATTTGAACCGGGG CTCCGGAGACCAACAAAACGAGGTAACTCCGGTGCACAGAGGGGGCACCCGGATTTGAACCGGGG A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:39154434..39154558 26863196 MeRIP-seq:(Medium) rs1007300123 Functional Loss SNV dbSNP153 33..33 33 - - - 108681 RMVar_ID_108681 Human_SNP_ID_623769517 m1A Human chr17 - 39154506 39154506 39154506 ATTTGACTGCAGATCAAGAGGTCCCCGGTTCAAATCCGGGTGCCCCCTCTGTGCTCCGGAGTTAC ATTTGACTGCAGATCAAGAGGTCCCCGGTTCAGATCCGGGTGCCCCCTCTGTGCTCCGGAGTTAC T C tRNA-Cys-GCA-2-2 RNACentral:URS0000417A0F tRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs960424170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488318,Human_RBP_ID_1547211,Human_RBP_ID_3521878,Human_RBP_ID_8451314,Human_RBP_ID_9885597,Human_RBP_ID_17081223,Human_RBP_ID_17380410,Human_RBP_ID_18696384,Human_RBP_ID_20293458,Human_RBP_ID_22056696,Human_RBP_ID_22213013,Human_RBP_ID_22960762,Human_RBP_ID_23129205,Human_RBP_ID_23724307,Human_RBP_ID_24417519,Human_RBP_ID_24481769,Human_RBP_ID_25341617,Human_RBP_ID_26460209,Human_RBP_ID_26959920,Human_RBP_ID_27253311 108682 RMVar_ID_108682 Human_SNP_ID_623775397 m1A Human chr17 - 39175166 39175166 39175166 CGCTGAGAGGCAGGGGCCACACGGCGGGAGGAAGGGCTCTGAGCCCAGGGGAGGGGAGGGAGCGA CGCTGAGAGGCAGGGGCCACACGGCGGGAGGATGGGCTCTGAGCCCAGGGGAGGGGAGGGAGCGA T A CACNB1 Ensembl:ENSG00000067191 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:39175115..39175343 26863196 MeRIP-seq:(Medium) rs766776561 Functional Loss SNV dbSNP153 33..33 33 - - - 108683 RMVar_ID_108683 Human_SNP_ID_623782668 m1A Human chr17 + 39201308 39201308 39201308 GTTAGACCCCAATGAGACCAATGAAATCGCCAATGCCAACTCCCGTGAGTACCTGGGATCTGTCT GTTAGACCCCAATGAGACCAATGAAATCGCCAGTGCCAACTCCCGTGAGTACCTGGGATCTGTCT A G RPL19 Ensembl:ENSG00000108298 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:39200550..39201373;chr17:39201096..39201325;chr17:39201182..39201362 26863196 MeRIP-seq:(Medium) rs755138997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_902101,Human_RBP_ID_1532955,Human_RBP_ID_1856928,Human_RBP_ID_3521891,Human_RBP_ID_8451328,Human_RBP_ID_9375809,Human_RBP_ID_12991660,Human_RBP_ID_17375362,Human_RBP_ID_17490868,Human_RBP_ID_18190797,Human_RBP_ID_18696408,Human_RBP_ID_19082347,Human_RBP_ID_22444493,Human_RBP_ID_23724353,Human_RBP_ID_26330714,Human_RBP_ID_26812207 Human_Splice_Rec_1810852,Human_Splice_Rec_1810853,Human_Splice_Rec_1810862,Human_Splice_Rec_1810863,Human_Splice_Rec_1810872,Human_Splice_Rec_1810873,Human_Splice_Rec_1810880,Human_Splice_Rec_1810881,Human_Splice_Rec_1810890,Human_Splice_Rec_1810891,Human_Splice_Rec_1810899 RMVar_hsa_circ_111948,RMVar_hsa_circ_125189,RMVar_hsa_circ_183862,RMVar_hsa_circ_183863 108684 RMVar_ID_108684 Human_SNP_ID_623782670 m1A Human chr17 - 39201321 39201321 39201321 AAGTAGGGTGAAGAGACAGATCCCAGGTACTCACGGGAGTTGGCATTGGCGATTTCATTGGTCTC AAGTAGGGTGAAGAGACAGATCCCAGGTACTCTCGGGAGTTGGCATTGGCGATTTCATTGGTCTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:39201201..39202083;chr17:39201301..39201325 32194978 MeRIP-seq:(Medium) rs112549869 Functional Loss SNV dbSNP153 33..33 33 - - - 108685 RMVar_ID_108685 Human_SNP_ID_623782671 m1A Human chr17 - 39201321 39201321 39201321 AAGTAGGGTGAAGAGACAGATCCCAGGTACTCACGGGAGTTGGCATTGGCGATTTCATTGGTCTC AAGTAGGGTGAAGAGACAGATCCCAGGTACTCGCGGGAGTTGGCATTGGCGATTTCATTGGTCTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:39201201..39202083;chr17:39201301..39201325 32194978 MeRIP-seq:(Medium) rs112549869 Functional Loss SNV dbSNP153 33..33 33 - - - 108686 RMVar_ID_108686 Human_SNP_ID_623783652 m1A Human chr17 + 39204607 39204607 39204607 GTGAAGAGCGCCTCCAGGCCAAGAAGGAGGAGATCATCAAGACTTTATCCAAGGAGGAAGAGACC GTGAAGAGCGCCTCCAGGCCAAGAAGGAGGAGGTCATCAAGACTTTATCCAAGGAGGAAGAGACC A G RPL19 Ensembl:ENSG00000108298 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:39204534..39204662 26863196 MeRIP-seq:(Medium) rs1333317919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488342,Human_RBP_ID_820497,Human_RBP_ID_902108,Human_RBP_ID_1007747,Human_RBP_ID_1181659,Human_RBP_ID_1286133,Human_RBP_ID_1532973,Human_RBP_ID_1856943,Human_RBP_ID_2529458,Human_RBP_ID_3521900,Human_RBP_ID_4472014,Human_RBP_ID_6590789,Human_RBP_ID_8253390,Human_RBP_ID_8451340,Human_RBP_ID_9071717,Human_RBP_ID_9375829,Human_RBP_ID_12991748,Human_RBP_ID_17259450,Human_RBP_ID_17375364,Human_RBP_ID_17490872,Human_RBP_ID_18291784,Human_RBP_ID_18438872,Human_RBP_ID_18530613,Human_RBP_ID_18696418,Human_RBP_ID_20172118,Human_RBP_ID_22056703,Human_RBP_ID_22213039,Human_RBP_ID_22499333,Human_RBP_ID_22804236,Human_RBP_ID_22950800,Human_RBP_ID_23114375,Human_RBP_ID_23129217,Human_RBP_ID_25279302,Human_RBP_ID_26330716,Human_RBP_ID_26450033,Human_RBP_ID_26813487,Human_RBP_ID_26959941,Human_RBP_ID_27253325,Human_RBP_ID_27664655 Human_Splice_Rec_1810860,Human_Splice_Rec_1810870,Human_Splice_Rec_1810878,Human_Splice_Rec_1810888,Human_Splice_Rec_1810898 Human_miRNA_ID_2063800,Human_miRNA_ID_2901462 RMVar_hsa_circ_89600,RMVar_hsa_circ_111948,RMVar_hsa_circ_125189,RMVar_hsa_circ_183862,RMVar_hsa_circ_183863,RMVar_hsa_circ_87350,RMVar_hsa_circ_93090,RMVar_hsa_circ_183864,RMVar_hsa_circ_97748,RMVar_hsa_circ_183865,RMVar_hsa_circ_183866,RMVar_hsa_circ_183867 108687 RMVar_ID_108687 Human_SNP_ID_623783701 m1A Human chr17 - 39204683 39204683 39204683 TTGTTTTATTTTAATGGCTGATCTATGTAATCACAGAGGCCAGTATGTACAGACAAAGTGGGAGG TTGTTTTATTTTAATGGCTGATCTATGTAATCGCAGAGGCCAGTATGTACAGACAAAGTGGGAGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:39204676..39204725 26863196 MeRIP-seq:(Medium) rs1464195337 Functional Loss SNV dbSNP153 33..33 33 - - - 108688 RMVar_ID_108688 Human_SNP_ID_623783711 m1A Human chr17 + 39204701 39204701 39204701 CATACTGGCCTCTGTGATTACATAGATCAGCCATTAAAATAAAACAAGCCTTAATCTGCCTTCCT CATACTGGCCTCTGTGATTACATAGATCAGCCGTTAAAATAAAACAAGCCTTAATCTGCCTTCCT A G RPL19 Ensembl:ENSG00000108298 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39204651..39204750 32194978 MeRIP-seq:(Medium) rs1448880541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488346,Human_RBP_ID_1007750,Human_RBP_ID_1181661,Human_RBP_ID_1532973,Human_RBP_ID_1856943,Human_RBP_ID_2505174,Human_RBP_ID_3521901,Human_RBP_ID_8451343,Human_RBP_ID_9375832,Human_RBP_ID_17259452,Human_RBP_ID_17654157,Human_RBP_ID_18291785,Human_RBP_ID_18696422,Human_RBP_ID_21890084,Human_RBP_ID_24417295,Human_RBP_ID_26331702,Human_RBP_ID_26450036,Human_RBP_ID_26642064 Human_miRNA_ID_257772,Human_miRNA_ID_261566 RMVar_hsa_circ_89600,RMVar_hsa_circ_111948,RMVar_hsa_circ_125189,RMVar_hsa_circ_183862,RMVar_hsa_circ_183863,RMVar_hsa_circ_87350,RMVar_hsa_circ_93090,RMVar_hsa_circ_183864,RMVar_hsa_circ_97748,RMVar_hsa_circ_183865,RMVar_hsa_circ_183866,RMVar_hsa_circ_183867 108689 RMVar_ID_108689 Human_SNP_ID_623783713 m1A Human chr17 - 39204703 39204703 39204703 AGAGGAAGGCAGATTAAGGCTTGTTTTATTTTAATGGCTGATCTATGTAATCACAGAGGCCAGTA AGAGGAAGGCAGATTAAGGCTTGTTTTATTTTGATGGCTGATCTATGTAATCACAGAGGCCAGTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:39204701..39204725 26863196 MeRIP-seq:(Medium) rs747467786 Functional Loss SNV dbSNP153 33..33 33 - - - 108690 RMVar_ID_108690 Human_SNP_ID_623785186 m1A Human chr17 - 39209795 39209795 39209795 GCTGGGGCACTGCTGGCGCTGCCCGGATGCAGAGTGGGGGCTGCCTTTCCTGATGAGCGCCCCCT GCTGGGGCACTGCTGGCGCTGCCCGGATGCAGCGTGGGGGCTGCCTTTCCTGATGAGCGCCCCCT T G lnc-STAC2-3 RNACentral:URS0000D5A462 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39209676..39209825 26863196 MeRIP-seq:(Medium) rs1426547866 Functional Loss SNV dbSNP153 33..33 33 - - - 108691 RMVar_ID_108691 Human_SNP_ID_623785242 m1A Human chr17 - 39209998 39209998 39209998 GGATGACTCAGTCGCCCCTGTCATCGGAGCCCAGCATGGAGGGGCCGCACCCCTCCCGCCGCCGC GGATGACTCAGTCGCCCCTGTCATCGGAGCCCGGCATGGAGGGGCCGCACCCCTCCCGCCGCCGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39209948..39210182 26863196 MeRIP-seq:(Medium) rs973256940 Functional Loss SNV dbSNP153 33..33 33 - - - 108692 RMVar_ID_108692 Human_SNP_ID_623785452 m1A Human chr17 - 39210757 39210757 39210757 CCCATCCTGGGCACAGTTACACCCTCCCATGCAGTGGGAGAAACACAGACCCTCGTACCCAAAGG CCCATCCTGGGCACAGTTACACCCTCCCATGCGGTGGGAGAAACACAGACCCTCGTACCCAAAGG T C STAC2 Ensembl:ENSG00000141750 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39210707..39210959 26863196 MeRIP-seq:(Medium) rs1220595206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_341229,Human_miRNA_ID_619676,Human_miRNA_ID_1693590 108693 RMVar_ID_108693 Human_SNP_ID_623787624 m1A Human chr17 - 39218027 39218027 39218027 ACGCCCCCAACCCCACTGCCCCCTCCCTCCCCACCACCCACAGCCTCGGACAGGGGCCTGGCTAC ACGCCCCCAACCCCACTGCCCCCTCCCTCCCCCCCACCCACAGCCTCGGACAGGGGCCTGGCTAC T G STAC2 Ensembl:ENSG00000141750 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39217148..39218040 26863196 MeRIP-seq:(Medium) rs1221153818 Functional Loss SNV dbSNP153 33..33 33 - - - 108694 RMVar_ID_108694 Human_SNP_ID_623787710 m1A Human chr17 - 39218175 39218175 39218175 GGCTCCCACTCACAGCTCCCTCTTTTTCTCCCAGCTCCAGCGATTCAAGCGCTCCCTCTCCCTCA GGCTCCCACTCACAGCTCCCTCTTTTTCTCCCCGCTCCAGCGATTCAAGCGCTCCCTCTCCCTCA T G STAC2 Ensembl:ENSG00000141750 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39218138..39225477 26863196 MeRIP-seq:(Medium) rs780085407 Functional Loss SNV dbSNP153 33..33 33 - - - 108695 RMVar_ID_108695 Human_SNP_ID_623838009 m1A Human chr17 + 39401441 39401441 39401441 GGCGGGTGCGGCCCGGGCCGGGCGCTGCGGCGAGCGGAGTGCACAGACCGGGGGCCCAGGACAGG GGCGGGTGCGGCCCGGGCCGGGCGCTGCGGCGCGCGGAGTGCACAGACCGGGGGCCCAGGACAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39401422..39401628 26863196 MeRIP-seq:(Medium) rs1381718041 Functional Loss SNV dbSNP153 33..33 33 - - - 108696 RMVar_ID_108696 Human_SNP_ID_623838254 m1A Human chr17 + 39402112 39402112 39402112 CCGCGCCCGTCGCCCCTCGTCACTTGTTCCCCAGGATCCTGTAAGGCACCCGCATCCTTCCCGGC CCGCGCCCGTCGCCCCTCGTCACTTGTTCCCCGGGATCCTGTAAGGCACCCGCATCCTTCCCGGC A G AC005288.1 Ensembl:ENSG00000266469 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39402067..39402279 26863196 MeRIP-seq:(Medium) rs1205280275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1811085 108697 RMVar_ID_108697 Human_SNP_ID_623838256 m1A Human chr17 + 39402115 39402115 39402115 CGCCCGTCGCCCCTCGTCACTTGTTCCCCAGGATCCTGTAAGGCACCCGCATCCTTCCCGGCCAC CGCCCGTCGCCCCTCGTCACTTGTTCCCCAGGTTCCTGTAAGGCACCCGCATCCTTCCCGGCCAC A T AC005288.1 Ensembl:ENSG00000266469 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39402091..39402187 26863196 MeRIP-seq:(Medium) rs981974463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1811085 108698 RMVar_ID_108698 Human_SNP_ID_623854363 m1A Human chr17 + 39461536 39461532 39461536 ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGAGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC ATCTAGTGTGTGACTGGGTCTGTGTGAGG____GAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC GGAGA G CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39461476..39461712 26863196 MeRIP-seq:(Medium) rs140413718 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_238018,Human_RBP_ID_262283,Human_RBP_ID_768627,Human_RBP_ID_896473,Human_RBP_ID_3522142,Human_RBP_ID_3950517,Human_RBP_ID_4466347,Human_RBP_ID_5114636,Human_RBP_ID_5420041,Human_RBP_ID_5441382,Human_RBP_ID_5525558,Human_RBP_ID_6591403,Human_RBP_ID_8232010,Human_RBP_ID_8825452,Human_RBP_ID_9289011,Human_RBP_ID_9346019,Human_RBP_ID_9375837,Human_RBP_ID_18419590,Human_RBP_ID_22061270,Human_RBP_ID_22357247,Human_RBP_ID_22443583,Human_RBP_ID_22740896,Human_RBP_ID_22960771,Human_RBP_ID_23724537,Human_RBP_ID_24545002,Human_RBP_ID_26330718,Human_RBP_ID_26769307,Human_RBP_ID_26960025,Human_RBP_ID_27812616 108699 RMVar_ID_108699 Human_SNP_ID_623854364 m1A Human chr17 + 39461536 39461532 39461536 ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGAGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC ATCTAGTGTGTGACTGGGTCTGTGTGAGGGA__GAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC GGAGA GGA CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39461476..39461712 26863196 MeRIP-seq:(Medium) rs140413718 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_238018,Human_RBP_ID_262283,Human_RBP_ID_768627,Human_RBP_ID_896473,Human_RBP_ID_3522142,Human_RBP_ID_3950517,Human_RBP_ID_4466347,Human_RBP_ID_5114636,Human_RBP_ID_5420041,Human_RBP_ID_5441382,Human_RBP_ID_5525558,Human_RBP_ID_6591403,Human_RBP_ID_8232010,Human_RBP_ID_8825452,Human_RBP_ID_9289011,Human_RBP_ID_9346019,Human_RBP_ID_9375837,Human_RBP_ID_18419590,Human_RBP_ID_22061270,Human_RBP_ID_22357247,Human_RBP_ID_22443583,Human_RBP_ID_22740896,Human_RBP_ID_22960771,Human_RBP_ID_23724537,Human_RBP_ID_24545002,Human_RBP_ID_26330718,Human_RBP_ID_26769307,Human_RBP_ID_26960025,Human_RBP_ID_27812616 108700 RMVar_ID_108700 Human_SNP_ID_623854368 m1A Human chr17 + 39461536 39461536 39461536 ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGAGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGGGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC A G CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39461476..39461712 26863196 MeRIP-seq:(Medium) rs373968044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238018,Human_RBP_ID_262283,Human_RBP_ID_768627,Human_RBP_ID_896473,Human_RBP_ID_3522142,Human_RBP_ID_3950517,Human_RBP_ID_4466347,Human_RBP_ID_5114636,Human_RBP_ID_5420041,Human_RBP_ID_5441382,Human_RBP_ID_5525558,Human_RBP_ID_6591403,Human_RBP_ID_8232010,Human_RBP_ID_8825452,Human_RBP_ID_9289011,Human_RBP_ID_9346019,Human_RBP_ID_9375837,Human_RBP_ID_18419590,Human_RBP_ID_22061270,Human_RBP_ID_22357247,Human_RBP_ID_22443583,Human_RBP_ID_22740896,Human_RBP_ID_22960771,Human_RBP_ID_23724537,Human_RBP_ID_24545002,Human_RBP_ID_26330718,Human_RBP_ID_26769307,Human_RBP_ID_26960025,Human_RBP_ID_27812616 108701 RMVar_ID_108701 Human_SNP_ID_623854369 m1A Human chr17 + 39461536 39461536 39461536 ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGAGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC ATCTAGTGTGTGACTGGGTCTGTGTGAGGGAGTGAGTGTGTGTGGTGTGGAGGTGAAACGGAGGC A T CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39461476..39461712 26863196 MeRIP-seq:(Medium) rs373968044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238018,Human_RBP_ID_262283,Human_RBP_ID_768627,Human_RBP_ID_896473,Human_RBP_ID_3522142,Human_RBP_ID_3950517,Human_RBP_ID_4466347,Human_RBP_ID_5114636,Human_RBP_ID_5420041,Human_RBP_ID_5441382,Human_RBP_ID_5525558,Human_RBP_ID_6591403,Human_RBP_ID_8232010,Human_RBP_ID_8825452,Human_RBP_ID_9289011,Human_RBP_ID_9346019,Human_RBP_ID_9375837,Human_RBP_ID_18419590,Human_RBP_ID_22061270,Human_RBP_ID_22357247,Human_RBP_ID_22443583,Human_RBP_ID_22740896,Human_RBP_ID_22960771,Human_RBP_ID_23724537,Human_RBP_ID_24545002,Human_RBP_ID_26330718,Human_RBP_ID_26769307,Human_RBP_ID_26960025,Human_RBP_ID_27812616 108702 RMVar_ID_108702 Human_SNP_ID_623854380 m1A Human chr17 + 39461572 39461572 39461572 TGTGTGTGGTGTGGAGGTGAAACGGAGGCAAGAAAGGGGGCTACCTCAGGAGCGAGGGACAAAGG TGTGTGTGGTGTGGAGGTGAAACGGAGGCAAGCAAGGGGGCTACCTCAGGAGCGAGGGACAAAGG A C CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:39461526..39461732 26863196 MeRIP-seq:(Medium) rs980971044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238018,Human_RBP_ID_262283,Human_RBP_ID_768627,Human_RBP_ID_896473,Human_RBP_ID_3950517,Human_RBP_ID_4466347,Human_RBP_ID_5114636,Human_RBP_ID_5318382,Human_RBP_ID_5420043,Human_RBP_ID_5441384,Human_RBP_ID_5525558,Human_RBP_ID_8232010,Human_RBP_ID_8825452,Human_RBP_ID_9289011,Human_RBP_ID_9327278,Human_RBP_ID_9375838,Human_RBP_ID_18419590,Human_RBP_ID_22061270,Human_RBP_ID_22357247,Human_RBP_ID_22443583,Human_RBP_ID_22740896,Human_RBP_ID_23118886,Human_RBP_ID_23724538,Human_RBP_ID_24545002,Human_RBP_ID_26330718,Human_RBP_ID_26769307,Human_RBP_ID_27451670,Human_RBP_ID_27812616 108703 RMVar_ID_108703 Human_SNP_ID_623854419 m1A Human chr17 + 39461725 39461725 39461725 TCGCAGGGCCCCAGAGCTGGAGTCGGCTCCACAGCCCCGGGCCGTCGGCTTCTCACTTCCTGGAC TCGCAGGGCCCCAGAGCTGGAGTCGGCTCCACGGCCCCGGGCCGTCGGCTTCTCACTTCCTGGAC A G CDK12 Ensembl:ENSG00000167258 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39461679..39461791 32194978 MeRIP-seq:(Medium) rs1308009375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238019,Human_RBP_ID_4423727,Human_RBP_ID_5420044,Human_RBP_ID_5441385,Human_RBP_ID_5466420,Human_RBP_ID_5498203,Human_RBP_ID_5525559,Human_RBP_ID_26960028,Human_RBP_ID_27451671,Human_RBP_ID_27560994 108704 RMVar_ID_108704 Human_SNP_ID_623857351 m1A Human chr17 + 39471501 39471501 39471501 CTCAGACACCCCCTTTGCCACCTTTGCCTCCAATACCAGCTCTTCCACAGCAACCACCTCTGCCT CTCAGACACCCCCTTTGCCACCTTTGCCTCCAGTACCAGCTCTTCCACAGCAACCACCTCTGCCT A G CDK12 Ensembl:ENSG00000167258 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:39471476..39471500;chr17:39471450..39471572 26863196 MeRIP-seq:(Medium) rs369655491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1857134,Human_RBP_ID_17490962,Human_RBP_ID_18696595,Human_RBP_ID_18941649,Human_RBP_ID_22062101 RMVar_hsa_circ_308828 108705 RMVar_ID_108705 Human_SNP_ID_623883684 m1A Human chr17 - 39573709 39573709 39573709 GCAGCCTGCCACGCACTGCGGGGGCACTGAGGAGCGGGGGCCGGTGCCAAGTCCGCCAGACGGTT GCAGCCTGCCACGCACTGCGGGGGCACTGAGGGGCGGGGGCCGGTGCCAAGTCCGCCAGACGGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39573703..39573863 26863196 MeRIP-seq:(Medium) rs1423072170 Functional Loss SNV dbSNP153 33..33 33 - - - 108706 RMVar_ID_108706 Human_SNP_ID_623905087 m1A Human chr17 + 39658240 39658240 39658240 TGCAGCTCTAGGAATCAGAAGGTTCTTTCTCCAGCCTAACCCCAGTTTATCCTGCTGCAGACTTG TGCAGCTCTAGGAATCAGAAGGTTCTTTCTCCTGCCTAACCCCAGTTTATCCTGCTGCAGACTTG A T STARD3 Ensembl:ENSG00000131748 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39658235..39658435 32194978 MeRIP-seq:(Medium) rs748664858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17080262,Human_RBP_ID_21975069 RMVar_hsa_circ_56574,RMVar_hsa_circ_30925,RMVar_hsa_circ_108596,RMVar_hsa_circ_183953 108707 RMVar_ID_108707 Human_SNP_ID_623905269 m1A Human chr17 - 39658769 39658769 39658769 TGAATAGAACTGTCCCTCGGACAGAGCACCGGAGAACAGCAGGGGTCCACGGGCAACAGCAACCT TGAATAGAACTGTCCCTCGGACAGAGCACCGGGGAACAGCAGGGGTCCACGGGCAACAGCAACCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39658682..39658782 32194978 MeRIP-seq:(Medium) rs761342749 Functional Loss SNV dbSNP153 33..33 33 - - - 108708 RMVar_ID_108708 Human_SNP_ID_623909478 m1A Human chr17 + 39672022 39672019 39672022 CACACACACTTTGAAGCCACACCTCTTCCCCGACAACACCCGTCTCCACACTGCGCACCTAGGCC CACACACACTTTGAAGCCACACCTCTTCCC___CAACACCCGTCTCCACACTGCGCACCTAGGCC CCGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:39671944..39672077;chr17:39671788..39672125 26863196 MeRIP-seq:(Medium) rs1268754218 Functional Loss DEL dbSNP153 31..33 33 - - - 108709 RMVar_ID_108709 Human_SNP_ID_623909546 m1A Human chr17 - 39672243 39672243 39672243 TGCTGGGATTGGGAAGGAGTTTCACCCTGACCATTGCCCTAGCCAGGTTCCCAGGAGGCCTCACC TGCTGGGATTGGGAAGGAGTTTCACCCTGACCGTTGCCCTAGCCAGGTTCCCAGGAGGCCTCACC T C PGAP3 Ensembl:ENSG00000161395 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2952151 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15215,GWAS_ID_15216,GWAS_ID_15217,GWAS_ID_15218,GWAS_ID_15219,GWAS_ID_15220,GWAS_ID_15221 108710 RMVar_ID_108710 Human_SNP_ID_623913615 m1A Human chr17 + 39688004 39688004 39688004 CTGCCCCAGCTAGCAGGACCAACCGCGCCGCCAGGCCGGCCATCCTTTCTCCCTGGCTCGCCGCC CTGCCCCAGCTAGCAGGACCAACCGCGCCGCCGGGCCGGCCATCCTTTCTCCCTGGCTCGCCGCC A G ERBB2 Ensembl:ENSG00000141736 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39687923..39688017 26863196 MeRIP-seq:(Medium) rs1327632908 Functional Loss SNV dbSNP153 33..33 33 - - - 108711 RMVar_ID_108711 Human_SNP_ID_623921155 m1A Human chr17 + 39715835 39715835 39715835 GGAACTGGGCAGTGGACTGGCCCTCATCCACCATAACACCCACCTCTGCTTCGTGCACACGGTGC GGAACTGGGCAGTGGACTGGCCCTCATCCACCGTAACACCCACCTCTGCTTCGTGCACACGGTGC A G ERBB2 Ensembl:ENSG00000141736 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39715784..39715885 32194978 MeRIP-seq:(Medium) rs201097345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820546,Human_RBP_ID_3522308 Human_Splice_Rec_1811910,Human_Splice_Rec_1811974,Human_Splice_Rec_1812002,Human_Splice_Rec_1812054,Human_Splice_Rec_1812094,Human_Splice_Rec_1812146,Human_Splice_Rec_1812186,Human_Splice_Rec_1812200,Human_Splice_Rec_1812224,Human_Splice_Rec_1812276,Human_Splice_Rec_1812348 Human_miRNA_ID_681425,Human_miRNA_ID_2273711 RMVar_hsa_circ_28605,RMVar_hsa_circ_88421,RMVar_hsa_circ_76121,RMVar_hsa_circ_183960,RMVar_hsa_circ_18257,RMVar_hsa_circ_183962,RMVar_hsa_circ_337371,RMVar_hsa_circ_33758,RMVar_hsa_circ_79779,RMVar_hsa_circ_346761,RMVar_hsa_circ_183968,RMVar_hsa_circ_183969,RMVar_hsa_circ_342032 108712 RMVar_ID_108712 Human_SNP_ID_623921632 m1A Human chr17 + 39717397 39717397 39717397 TTCTGCGTGGCCCGCTGCCCCAGCGGTGTGAAACCTGACCTCTCCTACATGCCCATCTGGAAGTT TTCTGCGTGGCCCGCTGCCCCAGCGGTGTGAAGCCTGACCTCTCCTACATGCCCATCTGGAAGTT A G ERBB2 Ensembl:ENSG00000141736 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39717348..39717499 32194978 MeRIP-seq:(Medium) rs538900246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18470029 Human_Splice_Rec_1811916,Human_Splice_Rec_1811917,Human_Splice_Rec_1811980,Human_Splice_Rec_1812008,Human_Splice_Rec_1812009,Human_Splice_Rec_1812060,Human_Splice_Rec_1812061,Human_Splice_Rec_1812100,Human_Splice_Rec_1812101,Human_Splice_Rec_1812152,Human_Splice_Rec_1812153,Human_Splice_Rec_1812202,Human_Splice_Rec_1812230,Human_Splice_Rec_1812231,Human_Splice_Rec_1812282,Human_Splice_Rec_1812283,Human_Splice_Rec_1812350,Human_Splice_Rec_1812351,Human_Splice_Rec_1812378,Human_Splice_Rec_1812379,Human_Splice_Rec_1812387,Human_Splice_Rec_1812395,Human_Splice_Rec_1812397 RMVar_hsa_circ_88421,RMVar_hsa_circ_76121,RMVar_hsa_circ_183960,RMVar_hsa_circ_183962,RMVar_hsa_circ_33758,RMVar_hsa_circ_79779,RMVar_hsa_circ_346761,RMVar_hsa_circ_183968,RMVar_hsa_circ_183969,RMVar_hsa_circ_183971,RMVar_hsa_circ_183970,RMVar_hsa_circ_90069,RMVar_hsa_circ_99973 108713 RMVar_ID_108713 Human_SNP_ID_623922331 m1A Human chr17 - 39720337 39720337 39720337 CCCTTATTCCTGTGCTTACTCAACAGCCCCCGACACCAGAACTTTGAAGACATCCTGGATTTCCT CCCTTATTCCTGTGCTTACTCAACAGCCCCCGTCACCAGAACTTTGAAGACATCCTGGATTTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39720330..39720497 26863196 MeRIP-seq:(Medium) rs1385285911 Functional Loss SNV dbSNP153 33..33 33 - - - 108714 RMVar_ID_108714 Human_SNP_ID_623923049 m1A Human chr17 - 39723425 39723425 39723425 CTCCGTTTCCTGCAGCAGTCTCCGCATCGTGTACTTCCGGATCTTCTGCTGCCGTCGCTTGATGA CTCCGTTTCCTGCAGCAGTCTCCGCATCGTGTGCTTCCGGATCTTCTGCTGCCGTCGCTTGATGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:39723375..39723543 26863196 MeRIP-seq:(Medium) rs752669313 Functional Loss SNV dbSNP153 33..33 33 - - - 108715 RMVar_ID_108715 Human_SNP_ID_623924311 m1A Human chr17 + 39727479 39727479 39727479 TGACCCCAGCCCTCTACAGCGGTACAGTGAGGACCCCACAGTACCCCTGCCCTCTGAGACTGATG TGACCCCAGCCCTCTACAGCGGTACAGTGAGGTCCCCACAGTACCCCTGCCCTCTGAGACTGATG A T ERBB2 Ensembl:ENSG00000141736 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:39727428..39727720 32194978 MeRIP-seq:(Medium) rs1207872588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1811939,Human_Splice_Rec_1812031,Human_Splice_Rec_1812083,Human_Splice_Rec_1812123,Human_Splice_Rec_1812253,Human_Splice_Rec_1812305 Human_miRNA_ID_1191995,Human_miRNA_ID_1373160 108716 RMVar_ID_108716 Human_SNP_ID_623924877 m1A Human chr17 + 39729264 39729264 39729264 CATCAGACAGGTATTACCGAGGCGAAGAGTGGACTGGGCTTTCGTGGGCACTTACCCTGGGAAGG CATCAGACAGGTATTACCGAGGCGAAGAGTGGCCTGGGCTTTCGTGGGCACTTACCCTGGGAAGG A C ERBB2 Ensembl:ENSG00000141736 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39729213..39729525 26863196 MeRIP-seq:(Medium) rs1241645232 Functional Loss SNV dbSNP153 33..33 33 - - - 108717 RMVar_ID_108717 Human_SNP_ID_623925219 m1A Human chr17 - 39730293 39730293 39730293 ATCCCCAGCCCAGCCCCATCTCTTGACTCCCCAGTGAACCCTGCGGCTTCGAGGCGACCTACCTG ATCCCCAGCCCAGCCCCATCTCTTGACTCCCCTGTGAACCCTGCGGCTTCGAGGCGACCTACCTG T A MIEN1 Ensembl:ENSG00000141741 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:39730272..39730525 26863196 MeRIP-seq:(Medium) rs112370016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466361,Human_RBP_ID_5115457,Human_RBP_ID_17654668,Human_RBP_ID_18991155,Human_RBP_ID_22442905,Human_RBP_ID_22499352,Human_RBP_ID_27253496 Human_Splice_Rec_1812411,Human_Splice_Rec_1812415,Human_Splice_Rec_1812425,Human_Splice_Rec_1812427 RMVar_hsa_circ_87475,RMVar_hsa_circ_183978 108718 RMVar_ID_108718 Human_SNP_ID_623925320 m1A Human chr17 - 39730474 39730474 39730474 AGCCGGCCGCGATGAGCGGGGAGCCGGGGCAGACGTCCGTAGCGCCCCCTCCCGAGGAGGTCGAG AGCCGGCCGCGATGAGCGGGGAGCCGGGGCAGGCGTCCGTAGCGCCCCCTCCCGAGGAGGTCGAG T C MIEN1 Ensembl:ENSG00000141741 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:39730176..39730525;chr17:39730176..39730550;chr17:39730176..39730538 26863196 MeRIP-seq:(Medium) rs938761982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4424294,Human_RBP_ID_5115458,Human_RBP_ID_5143525 Human_Splice_Rec_1812409,Human_Splice_Rec_1812423 Human_miRNA_ID_2152081,Human_miRNA_ID_2420547,Human_miRNA_ID_2455764 RMVar_hsa_circ_87475,RMVar_hsa_circ_183978 108719 RMVar_ID_108719 Human_SNP_ID_623927155 m1A Human chr17 - 39738004 39738004 39738004 CGCTTCTCTACAGGTGGTAGGAGGGTGTCCCGACTTCGGACAGAGAAGTCAGAGGCGGGGGGGAG CGCTTCTCTACAGGTGGTAGGAGGGTGTCCCGCCTTCGGACAGAGAAGTCAGAGGCGGGGGGGAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39737968..39738062 26863196 MeRIP-seq:(Medium) rs1030649101 Functional Loss SNV dbSNP153 33..33 33 - - - 108720 RMVar_ID_108720 Human_SNP_ID_623966306 m1A Human chr17 + 39907878 39907878 39907878 GACCCTTTTCACAGCCAGTGCTGTCCTGCTGGAACTGGCCAAGTCATTTAATTGTGCTTCCTAGG GACCCTTTTCACAGCCAGTGCTGTCCTGCTGGCACTGGCCAAGTCATTTAATTGTGCTTCCTAGG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39907834..39907939 32194978 MeRIP-seq:(Medium) rs1255057249 Functional Loss SNV dbSNP153 33..33 33 - - - 108721 RMVar_ID_108721 Human_SNP_ID_623969958 m1A Human chr17 + 39921579 39921579 39921579 TTTCTGTCACAGCTTCCCCATACCCCCGCAGGAGTCAGGGCCAAGTTGGACCTGTGCTTACAATG TTTCTGTCACAGCTTCCCCATACCCCCGCAGGCGTCAGGGCCAAGTTGGACCTGTGCTTACAATG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:39921545..39921703 26863196 MeRIP-seq:(Medium) rs1309108098 Functional Loss SNV dbSNP153 33..33 33 - - - 108722 RMVar_ID_108722 Human_SNP_ID_623970046 m1A Human chr17 + 39921928 39921928 39921928 CTGGCCCCCTCACCTCTGGAACCAAGCCATCTACACTCTACCCCATCTTTCCCCAACCTGACCCT CTGGCCCCCTCACCTCTGGAACCAAGCCATCTGCACTCTACCCCATCTTTCCCCAACCTGACCCT A G lnc-LRRC3C-2 RNACentral:URS00008BEC48 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:39921805..39922000 26863196 MeRIP-seq:(Medium) rs886835085 Functional Loss SNV dbSNP153 33..33 33 - - - 108723 RMVar_ID_108723 Human_SNP_ID_623970059 m1A Human chr17 + 39921965 39921965 39921965 CTACCCCATCTTTCCCCAACCTGACCCTCCCCACTCCCAACCAGGACCCACGGTGGGTTGCAGAG CTACCCCATCTTTCCCCAACCTGACCCTCCCCGCTCCCAACCAGGACCCACGGTGGGTTGCAGAG A G lnc-LRRC3C-2 RNACentral:URS00008BEC48 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:39921702..39922030 26863196 MeRIP-seq:(Medium) rs943781032 Functional Loss SNV dbSNP153 33..33 33 - - - 108724 RMVar_ID_108724 Human_SNP_ID_623970123 m1A Human chr17 - 39922301 39922278 39922301 ATTTTTTGATCTTTTCCTTTTGCTTTTTGAATAGAGACTCCATGGAGTTGGTCATGGAATGGGCT ATTTTTTGATCTTTTCCTTTTGCTTTTTGAAT_______________________GGAATGGGCT CATGACCAACTCCATGGAGTCTCT C ORMDL3 Ensembl:ENSG00000172057 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39921879..39924786 32194978 MeRIP-seq:(Medium) rs937954209 Functional Loss DEL dbSNP153 33..55 33 - - - Human_RBP_ID_488596,Human_RBP_ID_1533130,Human_RBP_ID_1857283,Human_RBP_ID_3522357,Human_RBP_ID_5115473,Human_RBP_ID_5143800,Human_RBP_ID_6592175,Human_RBP_ID_8451597,Human_RBP_ID_9071779,Human_RBP_ID_18291960,Human_RBP_ID_18459671,Human_RBP_ID_22062635,Human_RBP_ID_24417303,Human_RBP_ID_24478849 RMVar_hsa_circ_120111,RMVar_hsa_circ_183985 108725 RMVar_ID_108725 Human_SNP_ID_623970664 m1A Human chr17 - 39924116 39924116 39924116 GCCGTGGCATCTGGCTCTCCTACGTGCTGGCCATCGGTCTCCTCCACATCGTGCTGCTGAGCATC GCCGTGGCATCTGGCTCTCCTACGTGCTGGCCGTCGGTCTCCTCCACATCGTGCTGCTGAGCATC T C ORMDL3 Ensembl:ENSG00000172057 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39924066..39924181 26863196 MeRIP-seq:(Medium) rs779244951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488608,Human_RBP_ID_764088,Human_RBP_ID_4424422,Human_RBP_ID_18696808,Human_RBP_ID_22443599 Human_Splice_Rec_1813025,Human_Splice_Rec_1813031,Human_Splice_Rec_1813035,Human_Splice_Rec_1813045,Human_Splice_Rec_1813049,Human_Splice_Rec_1813055 Human_miRNA_ID_2370763,Human_miRNA_ID_2707047,Human_miRNA_ID_3041147 RMVar_hsa_circ_120111,RMVar_hsa_circ_183985 108726 RMVar_ID_108726 Human_SNP_ID_623971431 m1A Human chr17 - 39927254 39927254 39927254 ACGTCGGGAGGAGCGCCTCGGCTAGGGGTGGGAGGCGGGGAGCGGCTCGGCTTCGGGGATAAACG ACGTCGGGAGGAGCGCCTCGGCTAGGGGTGGGGGGCGGGGAGCGGCTCGGCTTCGGGGATAAACG T C ORMDL3 Ensembl:ENSG00000172057 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39927247..39927312 26863196 MeRIP-seq:(Medium) rs1257925323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3545392,Human_RBP_ID_8189618,Human_RBP_ID_9422322 108727 RMVar_ID_108727 Human_SNP_ID_623971536 m1A Human chr17 - 39927538 39927538 39927538 CAGCCGCGGGTTGTTACAGCTGCTGGAGCAGCAGCGGCCCCCGCTCCCGGGAACCGTTCCCGGGC CAGCCGCGGGTTGTTACAGCTGCTGGAGCAGCTGCGGCCCCCGCTCCCGGGAACCGTTCCCGGGC T A ORMDL3 Ensembl:ENSG00000172057 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:39927446..39927543 26863196 MeRIP-seq:(Medium) rs1309669841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767399,Human_RBP_ID_4464514,Human_RBP_ID_17691956,Human_RBP_ID_17891585,Human_RBP_ID_22443600 Human_Splice_Rec_1813023,Human_Splice_Rec_1813029 108728 RMVar_ID_108728 Human_SNP_ID_623985392 m1A Human chr17 + 39981011 39981011 39981011 GGAGGGCTCGGCGCGGCGCCGCGGCGCGGACAAGGCGAAACCGCCGCCCGGCGGAGGAGAACAAG GGAGGGCTCGGCGCGGCGCCGCGGCGCGGACAGGGCGAAACCGCCGCCCGGCGGAGGAGAACAAG A G PSMD3 Ensembl:ENSG00000108344 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:39980826..39981200 26863196 MeRIP-seq:(Medium) rs771728091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465351,Human_RBP_ID_9289013,Human_RBP_ID_9327281,Human_RBP_ID_22443602 RMVar_hsa_circ_113219,RMVar_hsa_circ_183986 108729 RMVar_ID_108729 Human_SNP_ID_623985404 m1A Human chr17 + 39981041 39981041 39981041 CAAGGCGAAACCGCCGCCCGGCGGAGGAGAACAAGAACCCCCACCGCCGCCGGCCCCCCAGGATG CAAGGCGAAACCGCCGCCCGGCGGAGGAGAACGAGAACCCCCACCGCCGCCGGCCCCCCAGGATG A G PSMD3 Ensembl:ENSG00000108344 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:39980963..39981236 26863196 MeRIP-seq:(Medium) rs1356813799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4472251,Human_RBP_ID_6592195,Human_RBP_ID_8253398,Human_RBP_ID_8451602,Human_RBP_ID_8824642,Human_RBP_ID_23724805 RMVar_hsa_circ_113219,RMVar_hsa_circ_183986 108730 RMVar_ID_108730 Human_SNP_ID_623985435 m1A Human chr17 - 39981109 39981109 39981109 CGCCGCCGTCTTGCCGTCTGCCTCCCCCGTCGACCCGCCACCCGTCGCTGCCTCCTCTTTCATCT CGCCGCCGTCTTGCCGTCTGCCTCCCCCGTCGGCCCGCCACCCGTCGCTGCCTCCTCTTTCATCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr17:39980826..39984422;chr17:39980912..39981206;chr17:39980801..39984416 26863196 MeRIP-seq:(Medium) rs1305963736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183987 108731 RMVar_ID_108731 Human_SNP_ID_623986381 m1A Human chr17 - 39984413 39984413 39984413 ATTTGAAGTGAAGAAGCCCTGCACAGCCTTATACAGAACATAGTGGTTGAGGCGGCGTGATGTGG ATTTGAAGTGAAGAAGCCCTGCACAGCCTTATGCAGAACATAGTGGTTGAGGCGGCGTGATGTGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:39984276..39984450 32194978 MeRIP-seq:(Medium) rs78909252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183987 108732 RMVar_ID_108732 Human_SNP_ID_623986955 m1A Human chr17 + 39986667 39986667 39986667 CCCCTCCTGCCTGAAGTGGAAGCCTATCTCCAACTCCTCGTGGTCATCTTCATGATGAACAGCAA CCCCTCCTGCCTGAAGTGGAAGCCTATCTCCAGCTCCTCGTGGTCATCTTCATGATGAACAGCAA A G PSMD3 Ensembl:ENSG00000108344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39986535..39986747 26863196 MeRIP-seq:(Medium) rs370395631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47158,Human_RBP_ID_903636,Human_RBP_ID_1368180,Human_RBP_ID_1533142,Human_RBP_ID_1857295,Human_RBP_ID_3522374,Human_RBP_ID_8451611,Human_RBP_ID_8817394,Human_RBP_ID_9287367,Human_RBP_ID_17259570,Human_RBP_ID_17891596,Human_RBP_ID_22443603,Human_RBP_ID_22804266,Human_RBP_ID_26960207 Human_Splice_Rec_1813128,Human_Splice_Rec_1813129,Human_Splice_Rec_1813148,Human_Splice_Rec_1813149,Human_Splice_Rec_1813169,Human_Splice_Rec_1813173 Human_miRNA_ID_1985313,Human_miRNA_ID_2089143,Human_miRNA_ID_2090014,Human_miRNA_ID_2940954 RMVar_hsa_circ_3245,RMVar_hsa_circ_113219,RMVar_hsa_circ_92561,RMVar_hsa_circ_183986,RMVar_hsa_circ_323197,RMVar_hsa_circ_353966,RMVar_hsa_circ_89938,RMVar_hsa_circ_183989,RMVar_hsa_circ_3124,RMVar_hsa_circ_183988 108733 RMVar_ID_108733 Human_SNP_ID_623986956 m1A Human chr17 + 39986667 39986667 39986667 CCCCTCCTGCCTGAAGTGGAAGCCTATCTCCAACTCCTCGTGGTCATCTTCATGATGAACAGCAA CCCCTCCTGCCTGAAGTGGAAGCCTATCTCCATCTCCTCGTGGTCATCTTCATGATGAACAGCAA A T PSMD3 Ensembl:ENSG00000108344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39986535..39986747 26863196 MeRIP-seq:(Medium) rs370395631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47158,Human_RBP_ID_903636,Human_RBP_ID_1368180,Human_RBP_ID_1533142,Human_RBP_ID_1857295,Human_RBP_ID_3522374,Human_RBP_ID_8451611,Human_RBP_ID_8817394,Human_RBP_ID_9287367,Human_RBP_ID_17259570,Human_RBP_ID_17891596,Human_RBP_ID_22443603,Human_RBP_ID_22804266,Human_RBP_ID_26960207 Human_Splice_Rec_1813128,Human_Splice_Rec_1813129,Human_Splice_Rec_1813148,Human_Splice_Rec_1813149,Human_Splice_Rec_1813169,Human_Splice_Rec_1813173 Human_miRNA_ID_1985313,Human_miRNA_ID_2089143,Human_miRNA_ID_2090014,Human_miRNA_ID_2940954 RMVar_hsa_circ_3245,RMVar_hsa_circ_113219,RMVar_hsa_circ_92561,RMVar_hsa_circ_183986,RMVar_hsa_circ_323197,RMVar_hsa_circ_353966,RMVar_hsa_circ_89938,RMVar_hsa_circ_183989,RMVar_hsa_circ_3124,RMVar_hsa_circ_183988 108734 RMVar_ID_108734 Human_SNP_ID_623989793 m1A Human chr17 - 39997749 39997749 39997749 CTGCCTGCTGTACAGTAAGTCACCGGCTGGGGAGGAGCCCTGGGGGAGGTCAGGGTGGCTGGCTC CTGCCTGCTGTACAGTAAGTCACCGGCTGGGGTGGAGCCCTGGGGGAGGTCAGGGTGGCTGGCTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:39997698..39997847;chr17:39997702..39997897 26863196 MeRIP-seq:(Medium) rs776079023 Functional Loss SNV dbSNP153 33..33 33 - - - 108735 RMVar_ID_108735 Human_SNP_ID_623989802 m1A Human chr17 - 39997764 39997764 39997764 TGCCTGCCCACCCTCCTGCCTGCTGTACAGTAAGTCACCGGCTGGGGAGGAGCCCTGGGGGAGGT TGCCTGCCCACCCTCCTGCCTGCTGTACAGTACGTCACCGGCTGGGGAGGAGCCCTGGGGGAGGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39997562..39997910 32194978 MeRIP-seq:(Medium) rs1568140448 Functional Loss SNV dbSNP153 33..33 33 - - - 108736 RMVar_ID_108736 Human_SNP_ID_623995971 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAA______________________ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 13..34 33 - - - 108737 RMVar_ID_108737 Human_SNP_ID_623995972 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACAC______________ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 21..34 33 - - - 108738 RMVar_ID_108738 Human_SNP_ID_623995973 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACACACAC__________ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 25..34 33 - - - 108739 RMVar_ID_108739 Human_SNP_ID_623995974 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACACACACAC________ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 27..34 33 - - - 108740 RMVar_ID_108740 Human_SNP_ID_623995975 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACACACACACAC______ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 29..34 33 - - - 108741 RMVar_ID_108741 Human_SNP_ID_623995976 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACACACACACACAC____ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 31..34 33 - - - 108742 RMVar_ID_108742 Human_SNP_ID_623995977 m1A Human chr17 + 40019196 40019175 40019197 AAATACACACAAACACACACACACACACACACACACACACATACACACTTTGCATCTAGAAAGTT AAATACACACAAACACACACACACACACACAC__ACACACATACACACTTTGCATCTAGAAAGTT AACACACACACACACACACACAC AACACACACACACACACACAC - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40019146..40019694 32194978 MeRIP-seq:(Medium) rs59767650 Functional Loss DEL dbSNP153 33..34 33 - - - 108743 RMVar_ID_108743 Human_SNP_ID_623997563 m1A Human chr17 - 40023644 40023644 40023644 AAAGAAAATGTGAATATCTGGCTGGAATGGCCAGGGGGAGGAAAGTCCCTCCCCAGTCCCTATTT AAAGAAAATGTGAATATCTGGCTGGAATGGCCGGGGGGAGGAAAGTCCCTCCCCAGTCCCTATTT T C MED24 Ensembl:ENSG00000008838 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40023641..40026245 32194978 MeRIP-seq:(Medium) rs1021112422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94153,RMVar_hsa_circ_184002,RMVar_hsa_circ_113893,RMVar_hsa_circ_184000,RMVar_hsa_circ_265673,RMVar_hsa_circ_77916,RMVar_hsa_circ_184001 108744 RMVar_ID_108744 Human_SNP_ID_623998309 m1A Human chr17 + 40026699 40026699 40026699 GGACCCCATTCTCCCAGGCATTGAGGATTTCCAAGATGGCGGCTGAGATGCTGAGACAGGCCTCA GGACCCCATTCTCCCAGGCATTGAGGATTTCCGAGATGGCGGCTGAGATGCTGAGACAGGCCTCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40026344..40026739 32194978 MeRIP-seq:(Medium) rs1489805352 Functional Loss SNV dbSNP153 33..33 33 - - - 108745 RMVar_ID_108745 Human_SNP_ID_624000774 m1A Human chr17 - 40035245 40035245 40035245 CTGCACGGCAGCCTCTGCAGAGCGGCTGCGGGAGGGGCTGGAGGCCGGCACTCCAGCCGCTGGGG CTGCACGGCAGCCTCTGCAGAGCGGCTGCGGGCGGGGCTGGAGGCCGGCACTCCAGCCGCTGGGG T G MED24 Ensembl:ENSG00000008838 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40035199..40035299 32194978 MeRIP-seq:(Medium) rs776864101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9378091,Human_RBP_ID_17891632 RMVar_hsa_circ_184002,RMVar_hsa_circ_113893,RMVar_hsa_circ_319914,RMVar_hsa_circ_346257,RMVar_hsa_circ_347766 108746 RMVar_ID_108746 Human_SNP_ID_624007868 m1A Human chr17 + 40063010 40063010 40063010 CCCGGGCGCAGGAGGCGGGCGGCCCGGGCCCCACCGGCCCCCCATGGACGCCCCCAGCACGGGGC CCCGGGCGCAGGAGGCGGGCGGCCCGGGCCCCCCCGGCCCCCCATGGACGCCCCCAGCACGGGGC A C THRA Ensembl:ENSG00000126351 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40062968..40063136 26863196 MeRIP-seq:(Medium) rs888298110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465354 Human_Splice_Rec_1813837,Human_Splice_Rec_1813855,Human_Splice_Rec_1813873 108747 RMVar_ID_108747 Human_SNP_ID_624007896 m1A Human chr17 + 40063085 40063085 40063085 CCGCGTCGCTGCCCAGCCCGGTCCGGCGCGCCACGCCGAGGTAAGGAGGAGGGAGCGAGGGGGCA CCGCGTCGCTGCCCAGCCCGGTCCGGCGCGCCGCGCCGAGGTAAGGAGGAGGGAGCGAGGGGGCA A G THRA Ensembl:ENSG00000126351 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40062976..40063123;chr17:40062956..40063134 26863196 MeRIP-seq:(Medium) rs1408482284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465354 Human_Splice_Rec_1813837,Human_Splice_Rec_1813855,Human_Splice_Rec_1813873 108748 RMVar_ID_108748 Human_SNP_ID_624010880 m1A Human chr17 + 40074246 40074246 40074246 TCCGAAGCTACTCCCCCAGCACACAGCCCGGGACCCACAAACCCAGCTTGCCCCCAGCCCTCCCA TCCGAAGCTACTCCCCCAGCACACAGCCCGGGGCCCACAAACCCAGCTTGCCCCCAGCCCTCCCA A G THRA Ensembl:ENSG00000126351 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40074140..40074275 26863196 MeRIP-seq:(Medium) rs113607723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9378094,Human_RBP_ID_23724925,Human_RBP_ID_27812633 Human_Splice_Rec_1813802,Human_Splice_Rec_1813806,Human_Splice_Rec_1813812,Human_Splice_Rec_1813820,Human_Splice_Rec_1813838,Human_Splice_Rec_1813856,Human_Splice_Rec_1813874,Human_Splice_Rec_1813890,Human_Splice_Rec_1813906 RMVar_hsa_circ_19999 108749 RMVar_ID_108749 Human_SNP_ID_624010930 m1A Human chr17 - 40074451 40074433 40074451 TCAATTCCATCCAGGATGCCCTCCAGCACGCCAAGAGACTGGGGTGGGCACACTGGCCCCCCCGG TCAATTCCATCCAGGATGCCCTCCAGCACGCC__________________CACTGGCCCCCCCGG GTGCCCACCCCAGTCTCTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40074401..40074550 26863196 MeRIP-seq:(Medium) rs1445832847 Functional Loss DEL dbSNP153 33..50 33 - - - 108750 RMVar_ID_108750 Human_SNP_ID_624015156 m1A Human chr17 + 40090070 40090067 40090071 GAAAAATACAAAAAAGAGAGAGCGAGCGATAGAGAGAGATGATATTAAGTTATTAACTGAGGCTG GAAAAATACAAAAAAGAGAGAGCGAGCGAT____AGAGATGATATTAAGTTATTAACTGAGGCTG TAGAG T THRA Ensembl:ENSG00000126351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40090019..40090511 26863196 MeRIP-seq:(Medium) rs1011839803 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_23724934 RMVar_hsa_circ_184008,RMVar_hsa_circ_118743 108751 RMVar_ID_108751 Human_SNP_ID_624015157 m1A Human chr17 + 40090070 40090067 40090071 GAAAAATACAAAAAAGAGAGAGCGAGCGATAGAGAGAGATGATATTAAGTTATTAACTGAGGCTG GAAAAATACAAAAAAGAGAGAGCGAGCGATAG__AGAGATGATATTAAGTTATTAACTGAGGCTG TAGAG TAG THRA Ensembl:ENSG00000126351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40090019..40090511 26863196 MeRIP-seq:(Medium) rs1011839803 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23724934 RMVar_hsa_circ_184008,RMVar_hsa_circ_118743 108752 RMVar_ID_108752 Human_SNP_ID_624015173 m1A Human chr17 - 40090124 40090123 40090124 AGGGGCAGCTCGCAAAGTGCATGGGGTGGTAAAGGGGGGGTCCTCCCCTCTGGTCAGCCTCAGTT AGGGGCAGCTCGCAAAGTGCATGGGGTGGTAA_GGGGGGGTCCTCCCCTCTGGTCAGCCTCAGTT CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40090077..40090253 26863196 MeRIP-seq:(Medium) rs1019383787 Functional Loss DEL dbSNP153 33..33 33 - - - 108753 RMVar_ID_108753 Human_SNP_ID_624015174 m1A Human chr17 - 40090124 40090124 40090124 AGGGGCAGCTCGCAAAGTGCATGGGGTGGTAAAGGGGGGGTCCTCCCCTCTGGTCAGCCTCAGTT AGGGGCAGCTCGCAAAGTGCATGGGGTGGTAAGGGGGGGGTCCTCCCCTCTGGTCAGCCTCAGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40090077..40090253 26863196 MeRIP-seq:(Medium) rs1421791339 Functional Loss SNV dbSNP153 33..33 33 - - - 108754 RMVar_ID_108754 Human_SNP_ID_624015558 m1A Human chr17 - 40091387 40091387 40091387 CCAGCAGGGTGGGACAGGCACATGCACAGGTGACAGCGGGTGCTCCTCCAGGCCCTCCACCCCTG CCAGCAGGGTGGGACAGGCACATGCACAGGTGTCAGCGGGTGCTCCTCCAGGCCCTCCACCCCTG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40091338..40091554 26863196 MeRIP-seq:(Medium) rs1365831881 Functional Loss SNV dbSNP153 33..33 33 - - - 108755 RMVar_ID_108755 Human_SNP_ID_624015715 m1A Human chr17 - 40091966 40091966 40091966 CCACCCTGCCTGCCCTAGTGCCCCGGGCCAATACTGGGGGAGGCATGCTGAGCACCCACATCAAG CCACCCTGCCTGCCCTAGTGCCCCGGGCCAATGCTGGGGGAGGCATGCTGAGCACCCACATCAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40091916..40092072 26863196 MeRIP-seq:(Medium) rs567181742 Functional Loss SNV dbSNP153 33..33 33 - - - 108756 RMVar_ID_108756 Human_SNP_ID_624015910 m1A Human chr17 + 40092411 40092411 40092411 TGGGGGGAGGGGGGTTGTGGCCAGAAACAGGGAAGGAGGTAGGTCTCTTCCCCAGGGAGGGGTGG TGGGGGGAGGGGGGTTGTGGCCAGAAACAGGGGAGGAGGTAGGTCTCTTCCCCAGGGAGGGGTGG A G THRA Ensembl:ENSG00000126351 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40092402..40092505 26863196 MeRIP-seq:(Medium) rs954592448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200505,Human_RBP_ID_3547416,Human_RBP_ID_5143195,Human_RBP_ID_5237635,Human_RBP_ID_8191051,Human_RBP_ID_9422856,Human_RBP_ID_18459672,Human_RBP_ID_26457497,Human_RBP_ID_26782243 Human_miRNA_ID_976074 RMVar_hsa_circ_184008,RMVar_hsa_circ_118743 108757 RMVar_ID_108757 Human_SNP_ID_624016297 m1A Human chr17 - 40093592 40093592 40093592 AGATGTTGCCAGGCAGAGAAAGGGGGAAGGGCATCCCAGGCAGAGGGAACTACACAGCAAAAAGC AGATGTTGCCAGGCAGAGAAAGGGGGAAGGGCGTCCCAGGCAGAGGGAACTACACAGCAAAAAGC T C NR1D1 Ensembl:ENSG00000126368 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40093542..40093703 26863196 MeRIP-seq:(Medium) rs1157926326 Functional Loss SNV dbSNP153 33..33 33 - - - 108758 RMVar_ID_108758 Human_SNP_ID_624017617 m1A Human chr17 + 40097284 40097284 40097284 GGTGAGGGAGCCAGTGGGGGATGGTGGGAAGTAGGTGGGACAGCCTTGGGTCAGGGACTGGAAGC GGTGAGGGAGCCAGTGGGGGATGGTGGGAAGTGGGTGGGACAGCCTTGGGTCAGGGACTGGAAGC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:40097242..40097368 26863196 MeRIP-seq:(Medium) rs780564280 Functional Loss SNV dbSNP153 33..33 33 - - - 108759 RMVar_ID_108759 Human_SNP_ID_624018577 m1A Human chr17 + 40100464 40100464 40100464 TGCGGGGTGGCGAATCTGGAGCTCCCGGTGCAAAAGTCCCAGAGGAAGAGAGGTTGCAACCAGGA TGCGGGGTGGCGAATCTGGAGCTCCCGGTGCAGAAGTCCCAGAGGAAGAGAGGTTGCAACCAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40100416..40100568 26863196 MeRIP-seq:(Medium) rs201361761 Functional Loss SNV dbSNP153 33..33 33 - - - 108760 RMVar_ID_108760 Human_SNP_ID_624024069 m1A Human chr17 - 40121709 40121709 40121709 GGGGAAGAAGGGCGAGGGCGGCCGCGGGAAGAAGGGGAAAGCGGAGGCTCCCCGGGAAAAAAGCG GGGGAAGAAGGGCGAGGGCGGCCGCGGGAAGACGGGGAAAGCGGAGGCTCCCCGGGAAAAAAGCG T G lnc-NR1D1-1,lnc-NR1D1-1:2,lnc-NR1D1-1:3,lnc-NR1D1-1:4,lnc-NR1D1-1:5,lnc-NR1D1-1:6,lnc-NR1D1-1:7,lnc-NR1D1-1:8,lnc-NR1D1-1:9,lnc-NR1D1-1:10 RNACentral:URS00008B80DC,RNACentral:URS00008C2224,RNACentral:URS0000D5A831,RNACentral:URS0000D5A2C4,RNACentral:URS0000D580D8,RNACentral:URS0000D5CADC,RNACentral:URS0000D5DAED,RNACentral:URS00008BE8F3,RNACentral:URS00008BC1AE,RNACentral:URS0000E43E09 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,intron,exon,exon,intron,intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr17:40121706..40121876;chr17:40121233..40121836 26863196 MeRIP-seq:(Medium) rs1362843706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17067928 108761 RMVar_ID_108761 Human_SNP_ID_624024286 m1A Human chr17 + 40122183 40122182 40122183 CCCTCCACCCCCTCCTGAGGAGGAGGGGGGGGAAATGGAGGCTCGGGGCGGTTGAGGCGAGCTCC CCCTCCACCCCCTCCTGAGGAGGAGGGGGGGG_AATGGAGGCTCGGGGCGGTTGAGGCGAGCTCC GA G MSL1 Ensembl:ENSG00000188895 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40121976..40122225 26863196 MeRIP-seq:(Medium) rs1247473407 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5496977 108762 RMVar_ID_108762 Human_SNP_ID_624024288 m1A Human chr17 + 40122183 40122183 40122183 CCCTCCACCCCCTCCTGAGGAGGAGGGGGGGGAAATGGAGGCTCGGGGCGGTTGAGGCGAGCTCC CCCTCCACCCCCTCCTGAGGAGGAGGGGGGGGGAATGGAGGCTCGGGGCGGTTGAGGCGAGCTCC A G MSL1 Ensembl:ENSG00000188895 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40121976..40122225 26863196 MeRIP-seq:(Medium) rs1288150674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5496977 108763 RMVar_ID_108763 Human_SNP_ID_624024362 m1A Human chr17 + 40122373 40122353 40122374 GCCTCTGAGGCGAAGGCGGCGGCGGCGGCAGCAGAGGCGGCGGCGAGGCCCCCATGGGCCGGCGG GCCTCTGAGGCGA_____________________AGGCGGCGGCGAGGCCCCCATGGGCCGGCGG AAGGCGGCGGCGGCGGCAGCAG A MSL1 Ensembl:ENSG00000188895 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:40122026..40122700 26863196 MeRIP-seq:(Medium) rs1421270252 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_899942,Human_RBP_ID_3542926,Human_RBP_ID_4464520,Human_RBP_ID_5318389,Human_RBP_ID_8189620,Human_RBP_ID_9289023,Human_RBP_ID_9327282,Human_RBP_ID_9353310,Human_RBP_ID_9422857,Human_RBP_ID_18419945,Human_RBP_ID_18460261,Human_RBP_ID_21974341,Human_RBP_ID_22063119 108764 RMVar_ID_108764 Human_SNP_ID_624024363 m1A Human chr17 + 40122354 40122354 40122354 CGGCTGGGTGCGAGCTCCTGCCTCTGAGGCGAAGGCGGCGGCGGCGGCAGCAGAGGCGGCGGCGA CGGCTGGGTGCGAGCTCCTGCCTCTGAGGCGACGGCGGCGGCGGCGGCAGCAGAGGCGGCGGCGA A C MSL1 Ensembl:ENSG00000188895 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40121976..40123387;chr17:40121976..40122834 26863196 MeRIP-seq:(Medium) rs987138896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238285,Human_RBP_ID_899942,Human_RBP_ID_3542926,Human_RBP_ID_4464520,Human_RBP_ID_5186138,Human_RBP_ID_5318389,Human_RBP_ID_8189620,Human_RBP_ID_9289023,Human_RBP_ID_9327282,Human_RBP_ID_9353310,Human_RBP_ID_9422324,Human_RBP_ID_17654679,Human_RBP_ID_18419945,Human_RBP_ID_18438915,Human_RBP_ID_18460261,Human_RBP_ID_18470043,Human_RBP_ID_21974341,Human_RBP_ID_22063119 108765 RMVar_ID_108765 Human_SNP_ID_624024383 m1A Human chr17 + 40122394 40122394 40122394 GCGGCGGCAGCAGAGGCGGCGGCGAGGCCCCCATGGGCCGGCGGCGGGCCTCAGCCGCGGCCTCC GCGGCGGCAGCAGAGGCGGCGGCGAGGCCCCCGTGGGCCGGCGGCGGGCCTCAGCCGCGGCCTCC A G MSL1 Ensembl:ENSG00000188895 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40122348..40122504 32194978 MeRIP-seq:(Medium) rs974808962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3545394,Human_RBP_ID_4464521,Human_RBP_ID_5319033,Human_RBP_ID_8189620,Human_RBP_ID_23257166 108766 RMVar_ID_108766 Human_SNP_ID_624024626 m1A Human chr17 + 40122972 40122966 40122972 AAGCAAGCCGGCATTGGGGGGGAGCCTGCCGCAGCCGGAGCCGGCTGCAGCCCCCGGCCCAAGTA AAGCAAGCCGGCATTGGGGGGGAGCCT______GCCGGAGCCGGCTGCAGCCCCCGGCCCAAGTA TGCCGCA T MSL1 Ensembl:ENSG00000188895 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40122926..40123275 26863196 MeRIP-seq:(Medium) rs1004486585 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_50985,Human_RBP_ID_767590,Human_RBP_ID_898469,Human_RBP_ID_4464523,Human_RBP_ID_5144158,Human_RBP_ID_8232598,Human_RBP_ID_9422325,Human_RBP_ID_18460262,Human_RBP_ID_22061295,Human_RBP_ID_22543226,Human_RBP_ID_22716534 108767 RMVar_ID_108767 Human_SNP_ID_624024684 m1A Human chr17 - 40123101 40123101 40123101 GGTGGGGGTCCCGCCGGGTCCGAGGCGGTGGCAGCGGGGGAGGCCGCCCCACCCTTGTCCCCAGC GGTGGGGGTCCCGCCGGGTCCGAGGCGGTGGCGGCGGGGGAGGCCGCCCCACCCTTGTCCCCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40122901..40123300 26863196 MeRIP-seq:(Medium) rs777237827 Functional Loss SNV dbSNP153 33..33 33 - - - 108768 RMVar_ID_108768 Human_SNP_ID_624025516 m1A Human chr17 - 40126270 40126270 40126270 TAGCTCTGTTTCCTCTCTCTCTTCAGTTTCATAGCCCTGAAACAGCTTGTGCCTTTCTTTCTCGT TAGCTCTGTTTCCTCTCTCTCTTCAGTTTCATTGCCCTGAAACAGCTTGTGCCTTTCTTTCTCGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40126219..40126352 26863196 MeRIP-seq:(Medium) rs1295568709 Functional Loss SNV dbSNP153 33..33 33 - - - 108769 RMVar_ID_108769 Human_SNP_ID_624026017 m1A Human chr17 + 40128192 40128189 40128192 ACTTTCTTGGGATGTGGTGGGGGAAGAAGGGAAGAAGAAAGAGGCTAGAGAATGCCAGCAGACAG ACTTTCTTGGGATGTGGTGGGGGAAGAAGG___GAAGAAAGAGGCTAGAGAATGCCAGCAGACAG GGAA G MSL1 Ensembl:ENSG00000188895 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40128189..40128299 26863196 MeRIP-seq:(Medium) rs1309430356 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_766638 RMVar_hsa_circ_79403,RMVar_hsa_circ_184010,RMVar_hsa_circ_73801,RMVar_hsa_circ_314471 108770 RMVar_ID_108770 Human_SNP_ID_624029434 m1A Human chr17 + 40140742 40140742 40140742 CCGAACCGGGGCCCTTCATCTGCGGCGGGTGGAGAGCGGGGGCGCCAAGAGTGCTGAGGAGTCGG CCGAACCGGGGCCCTTCATCTGCGGCGGGTGGGGAGCGGGGGCGCCAAGAGTGCTGAGGAGTCGG A G CASC3 Ensembl:ENSG00000108349 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40140337..40140820 26863196 MeRIP-seq:(Medium) rs770909452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200511,Human_RBP_ID_768173,Human_RBP_ID_4425001,Human_RBP_ID_9375888,Human_RBP_ID_27838439 Human_Splice_Rec_1814021,Human_Splice_Rec_1814035,Human_Splice_Rec_1814041,Human_Splice_Rec_1814067 108771 RMVar_ID_108771 Human_SNP_ID_624029445 m1A Human chr17 + 40140757 40140757 40140757 TCATCTGCGGCGGGTGGAGAGCGGGGGCGCCAAGAGTGCTGAGGAGTCGGAGTGTGTGAGTGCGC TCATCTGCGGCGGGTGGAGAGCGGGGGCGCCAGGAGTGCTGAGGAGTCGGAGTGTGTGAGTGCGC A G CASC3 Ensembl:ENSG00000108349 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:40140551..40140818;chr17:40140343..40140878 26863196 MeRIP-seq:(Medium) rs1334869826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200511,Human_RBP_ID_237605,Human_RBP_ID_768173,Human_RBP_ID_3952330,Human_RBP_ID_9375888,Human_RBP_ID_27813813,Human_RBP_ID_27838439 Human_Splice_Rec_1814021,Human_Splice_Rec_1814035,Human_Splice_Rec_1814041,Human_Splice_Rec_1814067 108772 RMVar_ID_108772 Human_SNP_ID_624030854 m1A Human chr17 + 40145510 40145510 40145510 TTTTTTAAAAAGAGAAAAAGCCCAGATAGAGAAGATAGAGAGCGTTTGGGAACTTGGGAGTAATT TTTTTTAAAAAGAGAAAAAGCCCAGATAGAGACGATAGAGAGCGTTTGGGAACTTGGGAGTAATT A C CASC3 Ensembl:ENSG00000108349 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40145508..40145603 26863196 MeRIP-seq:(Medium) rs1197974547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83012,RMVar_hsa_circ_184020,RMVar_hsa_circ_115012,RMVar_hsa_circ_184018,RMVar_hsa_circ_269704,RMVar_hsa_circ_98384,RMVar_hsa_circ_184019 108773 RMVar_ID_108773 Human_SNP_ID_624034983 m1A Human chr17 + 40161889 40161889 40161889 AAAGCCTGACACCAAAAGCACTGTGACTGGAGAGAGGCAAAGTGGGGACGGACAGGTTAGTACAT AAAGCCTGACACCAAAAGCACTGTGACTGGAGTGAGGCAAAGTGGGGACGGACAGGTTAGTACAT A T CASC3 Ensembl:ENSG00000108349 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:40161778..40162055 26863196 MeRIP-seq:(Medium) rs1243534051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6807,Human_RBP_ID_47173,Human_RBP_ID_200039,Human_RBP_ID_899948,Human_RBP_ID_3952332,Human_RBP_ID_12997351,Human_RBP_ID_21975087,Human_RBP_ID_24372658,Human_RBP_ID_24544856,Human_RBP_ID_24552289,Human_RBP_ID_26331740,Human_RBP_ID_27812640 Human_Splice_Rec_1814027,Human_Splice_Rec_1814047,Human_Splice_Rec_1814073 RMVar_hsa_circ_83012,RMVar_hsa_circ_184020,RMVar_hsa_circ_115012,RMVar_hsa_circ_184018,RMVar_hsa_circ_269704,RMVar_hsa_circ_98384,RMVar_hsa_circ_184022,RMVar_hsa_circ_289239,RMVar_hsa_circ_337960,RMVar_hsa_circ_377536,RMVar_hsa_circ_184019,RMVar_hsa_circ_340698,RMVar_hsa_circ_305293,RMVar_hsa_circ_184023,RMVar_hsa_circ_184021 108774 RMVar_ID_108774 Human_SNP_ID_624037090 m1A Human chr17 + 40169398 40169398 40169398 GCCCAGCAGCAGGTGCAGCCAAAGCCCTCCCCACCCCGGAGGACTCCCCAGCCAGTCACCATCAA GCCCAGCAGCAGGTGCAGCCAAAGCCCTCCCCGCCCCGGAGGACTCCCCAGCCAGTCACCATCAA A G CASC3 Ensembl:ENSG00000108349 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:40169353..40170489 32194978 MeRIP-seq:(Medium) rs1371635142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27838440 Human_Splice_Rec_1814062,Human_Splice_Rec_1814063,Human_Splice_Rec_1814094,Human_Splice_Rec_1814095 Human_miRNA_ID_251056,Human_miRNA_ID_794073,Human_miRNA_ID_820598,Human_miRNA_ID_842831,Human_miRNA_ID_2367988,Human_miRNA_ID_2367989,Human_miRNA_ID_2685766,Human_miRNA_ID_2726394,Human_miRNA_ID_3015773,Human_miRNA_ID_3015774 RMVar_hsa_circ_116019,RMVar_hsa_circ_97447,RMVar_hsa_circ_184025,RMVar_hsa_circ_184029,RMVar_hsa_circ_106680,RMVar_hsa_circ_184028,RMVar_hsa_circ_32318,RMVar_hsa_circ_356010 108775 RMVar_ID_108775 Human_SNP_ID_624039306 m1A Human chr17 + 40177893 40177893 40177893 CATGAAGCCGCTGGAGAAATTTCTGAAGAAGCAGACGTCGCAGCTGGCGGGCCGAACGGTGGCGG CATGAAGCCGCTGGAGAAATTTCTGAAGAAGCCGACGTCGCAGCTGGCGGGCCGAACGGTGGCGG A C RAPGEFL1 Ensembl:ENSG00000108352 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40177846..40177935 26863196 MeRIP-seq:(Medium) rs1461328708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18438925 108776 RMVar_ID_108776 Human_SNP_ID_624050745 m1A Human chr17 - 40219368 40219368 40219368 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCTTTTGCCAACCCGGAAATGGATCTG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCTTTTGCCAACCCGGAAATGGATCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:40219303..40220419;chr17:40219324..40260629;chr17:40219301..40260655;chr17:40219301..40220419;chr17:40219308..40219561 26863196 MeRIP-seq:(Medium) rs879141289 Functional Loss SNV dbSNP153 33..33 33 - - - 108777 RMVar_ID_108777 Human_SNP_ID_624050746 m1A Human chr17 - 40219368 40219368 40219368 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCTTTTGCCAACCCGGAAATGGATCTG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCCCTTTTGCCAACCCGGAAATGGATCTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:40219303..40220419;chr17:40219324..40260629;chr17:40219301..40260655;chr17:40219301..40220419;chr17:40219308..40219561 26863196 MeRIP-seq:(Medium) rs879141289 Functional Loss SNV dbSNP153 33..33 33 - - - 108778 RMVar_ID_108778 Human_SNP_ID_624050750 m1A Human chr17 + 40219400 40219373 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGG___________________________CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGGCGGCGGCGGCGGCGGCGGCGGCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs1329923378 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108779 RMVar_ID_108779 Human_SNP_ID_624050752 m1A Human chr17 + 40219400 40219376 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGG________________________CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGGCGGCGGCGGCGGCGGCGGCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs991263205 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108780 RMVar_ID_108780 Human_SNP_ID_624050755 m1A Human chr17 + 40219400 40219379 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGGCGG_____________________CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGGCGGCGGCGGCGGCGGCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs920615231 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108781 RMVar_ID_108781 Human_SNP_ID_624050768 m1A Human chr17 + 40219400 40219391 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGGCGGCGGCGGCGGCGG_________CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGGCGGCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs934832720 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108782 RMVar_ID_108782 Human_SNP_ID_624050777 m1A Human chr17 + 40219400 40219394 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGGCGGCGGCGGCGGCGGCGG______CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGGCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs1555557765 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108783 RMVar_ID_108783 Human_SNP_ID_624050783 m1A Human chr17 + 40219400 40219397 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGGCGGCGGCGGCGGCGGCGGCGG___CGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG GCGA G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs760099763 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108784 RMVar_ID_108784 Human_SNP_ID_624050790 m1A Human chr17 + 40219400 40219400 40219400 TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGACGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG TGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGAGAAAGAGCTTGCCGGGGGGCGAGCAG A G WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40219358..40219482 26863196 MeRIP-seq:(Medium) rs565192365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767800,Human_RBP_ID_4472437,Human_RBP_ID_18419593,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814311 108785 RMVar_ID_108785 Human_SNP_ID_624050820 m1A Human chr17 + 40219449 40219449 40219449 GCCGGGGGGCGAGCAGGACAGGACGAAGCCGGAGTGTAGGCGGCAGAGGATTCGCTCCCAGAGCA GCCGGGGGGCGAGCAGGACAGGACGAAGCCGGCGTGTAGGCGGCAGAGGATTCGCTCCCAGAGCA A C WIPF2 Ensembl:ENSG00000171475 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chr17:40219398..40219525;chr17:40219372..40219457 26863196,26863410 MeRIP-seq:(Medium) rs1235315242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1533347,Human_RBP_ID_18419594,Human_RBP_ID_27812651 Human_Splice_Rec_1814251,Human_Splice_Rec_1814257,Human_Splice_Rec_1814271,Human_Splice_Rec_1814283,Human_Splice_Rec_1814297,Human_Splice_Rec_1814311 108786 RMVar_ID_108786 Human_SNP_ID_624050892 m1A Human chr17 - 40219646 40219646 40219646 ACAGTCCCCCGGCCCCCCGCCCCTCAGGCCCCACCCGCAAGACCCCTCTCCCCCTCCGGCCCCTC ACAGTCCCCCGGCCCCCCGCCCCTCAGGCCCCCCCCGCAAGACCCCTCTCCCCCTCCGGCCCCTC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:40219644..40220001 26863196 MeRIP-seq:(Medium) rs924122930 Functional Loss SNV dbSNP153 33..33 33 - - - 108787 RMVar_ID_108787 Human_SNP_ID_624063731 m1A Human chr17 + 40264763 40264763 40264763 TGCCAACGCACCCCCCACACCTCTGCCTATGCACAGCAGCAAAGCCCCCGCCTACAACAGAGAGA TGCCAACGCACCCCCCACACCTCTGCCTATGCGCAGCAGCAAAGCCCCCGCCTACAACAGAGAGA A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40264660..40265010 26863196 MeRIP-seq:(Medium) rs200852275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22804336 Human_miRNA_ID_352466,Human_miRNA_ID_681432,Human_miRNA_ID_1290309 RMVar_hsa_circ_2208,RMVar_hsa_circ_327377 108788 RMVar_ID_108788 Human_SNP_ID_624066041 m1A Human chr17 + 40273915 40273915 40273915 GCCGAGGAAAGCCCCCACCTCCACCCTCAAGGACGCCAGCTGGGCCACCCCCTCCTCCTCCACCG GCCGAGGAAAGCCCCCACCTCCACCCTCAAGGGCGCCAGCTGGGCCACCCCCTCCTCCTCCACCG A G WIPF2 Ensembl:ENSG00000171475 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40273751..40273974 26863196 MeRIP-seq:(Medium) rs1278037969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17263943,Human_RBP_ID_17378327,Human_RBP_ID_18697070 Human_Splice_Rec_1814255,Human_Splice_Rec_1814267,Human_Splice_Rec_1814279,Human_Splice_Rec_1814293,Human_Splice_Rec_1814307,Human_Splice_Rec_1814317,Human_Splice_Rec_1814331,Human_Splice_Rec_1814345 RMVar_hsa_circ_327377,RMVar_hsa_circ_367753 108789 RMVar_ID_108789 Human_SNP_ID_624069762 m1A Human chr17 + 40287975 40287975 40287975 TGTGGTGGTGAGTCCGAGAGGCTGCGTGTGAGAGACGTGAGAAGGATCCTGCACTGAGGAGGTGG TGTGGTGGTGAGTCCGAGAGGCTGCGTGTGAGTGACGTGAGAAGGATCCTGCACTGAGGAGGTGG A T CDC6 Ensembl:ENSG00000094804 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:40287864..40288163 26863196 MeRIP-seq:(Medium) rs1323353215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6811,Human_RBP_ID_237584,Human_RBP_ID_4464524,Human_RBP_ID_6592967,Human_RBP_ID_9375900,Human_RBP_ID_12998860,Human_RBP_ID_18419947,Human_RBP_ID_18697095,Human_RBP_ID_18991213,Human_RBP_ID_22061305,Human_RBP_ID_22445438,Human_RBP_ID_22959805,Human_RBP_ID_23209932,Human_RBP_ID_23725344 Human_Splice_Rec_1814371 108790 RMVar_ID_108790 Human_SNP_ID_624069766 m1A Human chr17 - 40287989 40287989 40287989 CAATCCTCTTCTTTCCACCTCCTCAGTGCAGGATCCTTCTCACGTCTCTCACACGCAGCCTCTCG CAATCCTCTTCTTTCCACCTCCTCAGTGCAGGTTCCTTCTCACGTCTCTCACACGCAGCCTCTCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:40287851..40288196;chr17:40287868..40288031;chr17:40287851..40288349;chr17:40287851..40288346;chr17:40287851..40288328 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1369647532 Functional Loss SNV dbSNP153 33..33 33 - - - 108791 RMVar_ID_108791 Human_SNP_ID_624069767 m1A Human chr17 - 40287989 40287989 40287989 CAATCCTCTTCTTTCCACCTCCTCAGTGCAGGATCCTTCTCACGTCTCTCACACGCAGCCTCTCG CAATCCTCTTCTTTCCACCTCCTCAGTGCAGGGTCCTTCTCACGTCTCTCACACGCAGCCTCTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:40287851..40288196;chr17:40287868..40288031;chr17:40287851..40288349;chr17:40287851..40288346;chr17:40287851..40288328 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1369647532 Functional Loss SNV dbSNP153 33..33 33 - - - 108792 RMVar_ID_108792 Human_SNP_ID_624070084 m1A Human chr17 - 40289355 40289355 40289355 GGACAACTAGTCAATATGTGAAAGTGAAGAGAAAATAACTAACATGGAATTTATTTATACTGATG GGACAACTAGTCAATATGTGAAAGTGAAGAGACAATAACTAACATGGAATTTATTTATACTGATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40289352..40289638 26863196 MeRIP-seq:(Medium) rs4134999 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - 108793 RMVar_ID_108793 Human_SNP_ID_624070449 m1A Human chr17 + 40290714 40290706 40290714 ACTAGTGGGTGGATAGCATATACAGTGTGGATATGCTGGCTGAAGGGATGATTCATGTCTTGGGT ACTAGTGGGTGGATAGCATATACAG________TGCTGGCTGAAGGGATGATTCATGTCTTGGGT GTGTGGATA G CDC6 Ensembl:ENSG00000094804 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40289347..40291095 26863196 MeRIP-seq:(Medium) rs957142050 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_12998949 RMVar_hsa_circ_10654,RMVar_hsa_circ_311171,RMVar_hsa_circ_26157 108794 RMVar_ID_108794 Human_SNP_ID_624071719 m1A Human chr17 + 40295394 40295394 40295394 AGAGATCAGGTTCTGGACAATGCTGCAGTTCAATTCTGTGCCCGCAAAGTCTCTGCTGTTTCAGG AGAGATCAGGTTCTGGACAATGCTGCAGTTCAGTTCTGTGCCCGCAAAGTCTCTGCTGTTTCAGG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1340785197 Functional Loss SNV dbSNP153 33..33 33 - - - 108795 RMVar_ID_108795 Human_SNP_ID_624072977 m1A Human chr17 - 40301032 40301032 40301032 CTACCTCCGTTCCATCTGCTCCATCCCAACTTACCTTCCCCAGAGTGACCTCTTTGATTTTCAAC CTACCTCCGTTCCATCTGCTCCATCCCAACTTTCCTTCCCCAGAGTGACCTCTTTGATTTTCAAC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:40300984..40301973 32194978 MeRIP-seq:(Medium) rs1391516721 Functional Loss SNV dbSNP153 33..33 33 - - - 108796 RMVar_ID_108796 Human_SNP_ID_624077091 m1A Human chr17 - 40318304 40318270 40318305 TCCAGGGGGCCGCGGCTCAGGGGCGCGGGGCGATGGCAGCGGCCATAGCGAGTCACGTGCGGAGG TCCAGGGGGCCGCGGCTCAGGGGCGCGGGGC__________________________________ AGCCTCCGCACGTGACTCGCTATGGCCGCTGCCATC A AC080112.5 Ensembl:ENSG00000287644 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:40318280..40318450;chr17:40318251..40318429 26863196 MeRIP-seq:(Medium) rs1441554105 Functional Loss DEL dbSNP153 32..65 33 - - - Human_Splice_Rec_1814515 108797 RMVar_ID_108797 Human_SNP_ID_624077118 m1A Human chr17 + 40318375 40318375 40318375 CTCTCCCGGGACCCCGCACCCTGATGCCGAGCAGCACCAGGGCGCCGGGTTAGGGCAGACGCTGT CTCTCCCGGGACCCCGCACCCTGATGCCGAGCGGCACCAGGGCGCCGGGTTAGGGCAGACGCTGT A G RARA Ensembl:ENSG00000131759 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40318276..40318450 26863410 MeRIP-seq:(Medium) rs772135862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466378 Human_Splice_Rec_1814431,Human_Splice_Rec_1814447 108798 RMVar_ID_108798 Human_SNP_ID_624082482 m1A Human chr17 + 40341633 40341633 40341633 ATGTCACGGGCAGCGGTGGGTGGGTCACTCGGAGGTGAGGCGCCGCCAGGCGAGTTCAGCGAGAG ATGTCACGGGCAGCGGTGGGTGGGTCACTCGGGGGTGAGGCGCCGCCAGGCGAGTTCAGCGAGAG A G RARA Ensembl:ENSG00000131759 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40341544..40341680 26863196 MeRIP-seq:(Medium) rs1342238541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3542942,Human_RBP_ID_8189628 108799 RMVar_ID_108799 Human_SNP_ID_624086912 m1A Human chr17 + 40357378 40357378 40357378 ACACACACACACTGGACAGTAGATGGGCCGACACACACTTGGCCCGAGTTCCTCCATTTCCCTGG ACACACACACACTGGACAGTAGATGGGCCGACCCACACTTGGCCCGAGTTCCTCCATTTCCCTGG A C RARA Ensembl:ENSG00000131759 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40357328..40357399 26863196 MeRIP-seq:(Medium) rs1289390152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17891889 Human_miRNA_ID_322569 108800 RMVar_ID_108800 Human_SNP_ID_624088372 m1A Human chr17 + 40362916 40362916 40362916 CGGGGTCCGGCCCTCGCCGTCCAGTCCGCGCGAGGCGGTGCCCGCCCCTAGATGGCCAGATCTCG CGGGGTCCGGCCCTCGCCGTCCAGTCCGCGCGGGGCGGTGCCCGCCCCTAGATGGCCAGATCTCG A G AC080112.2 Ensembl:ENSG00000266208 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40362879..40363198 26863196 MeRIP-seq:(Medium) rs561145608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901874,Human_RBP_ID_4464525 108801 RMVar_ID_108801 Human_SNP_ID_624088438 m1A Human chr17 + 40363067 40363067 40363067 CGCACGGCTCGGGGCCGGGGCGCCGGGAGGGCAGGGCCGGTGGCGGAGGTGGCGGCGGCGGCGGC CGCACGGCTCGGGGCCGGGGCGCCGGGAGGGCGGGGCCGGTGGCGGAGGTGGCGGCGGCGGCGGC A G AC080112.2 Ensembl:ENSG00000266208 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40362889..40363335 26863196 MeRIP-seq:(Medium) rs1476943010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819692,Human_RBP_ID_4466383 108802 RMVar_ID_108802 Human_SNP_ID_624088977 m1A Human chr17 - 40364526 40364524 40364527 CTGTGTAAGTGTGGGGTGGGGAGGATCTCAGGAGATGTGGAGGCTGGAGGCACAGGAGGCCAGGG CTGTGTAAGTGTGGGGTGGGGAGGATCTCAG___ATGTGGAGGCTGGAGGCACAGGAGGCCAGGG TCTC T GJD3 Ensembl:ENSG00000183153 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40364477..40364546;chr17:40364408..40364564 26863196 MeRIP-seq:(Medium) rs1441223621 Functional Loss DEL dbSNP153 32..34 33 - - - 108803 RMVar_ID_108803 Human_SNP_ID_624088978 m1A Human chr17 - 40364526 40364526 40364526 CTGTGTAAGTGTGGGGTGGGGAGGATCTCAGGAGATGTGGAGGCTGGAGGCACAGGAGGCCAGGG CTGTGTAAGTGTGGGGTGGGGAGGATCTCAGGCGATGTGGAGGCTGGAGGCACAGGAGGCCAGGG T G GJD3 Ensembl:ENSG00000183153 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40364477..40364546;chr17:40364408..40364564 26863196 MeRIP-seq:(Medium) rs973990786 Functional Loss SNV dbSNP153 33..33 33 - - - 108804 RMVar_ID_108804 Human_SNP_ID_624109575 m1A Human chr17 - 40443486 40443479 40443486 GCGCTGCGCCGCATCCTCGGCCCGGCCCAGGCAGGCGGCGGGCGGCGAGGGGCAGGGGGCTGAGC GCGCTGCGCCGCATCCTCGGCCCGGCCCAGGC_______GGGCGGCGAGGGGCAGGGGGCTGAGC CGCCGCCT C lnc-TNS4-4 RNACentral:URS0000D5B1BB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40443426..40443725;chr17:40443426..40443762 26863196 MeRIP-seq:(Medium) rs1255685339 Functional Loss DEL dbSNP153 33..39 33 - - - 108805 RMVar_ID_108805 Human_SNP_ID_624109583 m1A Human chr17 - 40443486 40443486 40443486 GCGCTGCGCCGCATCCTCGGCCCGGCCCAGGCAGGCGGCGGGCGGCGAGGGGCAGGGGGCTGAGC GCGCTGCGCCGCATCCTCGGCCCGGCCCAGGCGGGCGGCGGGCGGCGAGGGGCAGGGGGCTGAGC T C lnc-TNS4-4 RNACentral:URS0000D5B1BB lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:40443426..40443725;chr17:40443426..40443762 26863196 MeRIP-seq:(Medium) rs1002620304 Functional Loss SNV dbSNP153 33..33 33 - - - 108806 RMVar_ID_108806 Human_SNP_ID_624109589 m1A Human chr17 + 40443502 40443502 40443502 CTCGCCGCCCGCCGCCTGCCTGGGCCGGGCCGAGGATGCGGCGCAGCGCCTCGGCGGCCAGGCTT CTCGCCGCCCGCCGCCTGCCTGGGCCGGGCCGGGGATGCGGCGCAGCGCCTCGGCGGCCAGGCTT A G IGFBP4 Ensembl:ENSG00000141753 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Starvation treatment;HEPG2 cell line,mRNA heat shock 4h chr17:40443451..40443825;chr17:40443451..40443625;chr17:40443479..40443761;chr17:40443451..40443725 26863196,26863410,26863196 MeRIP-seq:(Medium) rs990997679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_765683,Human_RBP_ID_821081,Human_RBP_ID_4464530 RMVar_hsa_circ_109454,RMVar_hsa_circ_184075 108807 RMVar_ID_108807 Human_SNP_ID_624109595 m1A Human chr17 + 40443514 40443514 40443514 CGCCTGCCTGGGCCGGGCCGAGGATGCGGCGCAGCGCCTCGGCGGCCAGGCTTGCTCCCCTCCGG CGCCTGCCTGGGCCGGGCCGAGGATGCGGCGCGGCGCCTCGGCGGCCAGGCTTGCTCCCCTCCGG A G IGFBP4 Ensembl:ENSG00000141753 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40443451..40443575 26863410 MeRIP-seq:(Medium) rs978775660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821081,Human_RBP_ID_4464530 RMVar_hsa_circ_109454,RMVar_hsa_circ_184075 108808 RMVar_ID_108808 Human_SNP_ID_624121271 m1A Human chr17 - 40488892 40488892 40488892 ATGGCCCCCAGCACTGCTCCAGCCCCTCTGTCACCCCGCCCTTCGGCTCCCTTCGCAGTGGTGGC ATGGCCCCCAGCACTGCTCCAGCCCCTCTGTCGCCCCGCCCTTCGGCTCCCTTCGCAGTGGTGGC T C TNS4 Ensembl:ENSG00000131746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40488842..40488936 26863196 MeRIP-seq:(Medium) rs1267187218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24372671 Human_Splice_Rec_1814622 RMVar_hsa_circ_81210,RMVar_hsa_circ_88410,RMVar_hsa_circ_184086,RMVar_hsa_circ_184082,RMVar_hsa_circ_105890,RMVar_hsa_circ_94405,RMVar_hsa_circ_82755,RMVar_hsa_circ_184089,RMVar_hsa_circ_184090,RMVar_hsa_circ_184094 108809 RMVar_ID_108809 Human_SNP_ID_624134672 m1A Human chr17 - 40542540 40542539 40542540 CTTGAACCTCCCTAAGGGAGGCCTGGGGGGTTAGGGGGGAGTGGAAGGACGGGGGCTCATTTCCA CTTGAACCTCCCTAAGGGAGGCCTGGGGGGTT_GGGGGGAGTGGAAGGACGGGGGCTCATTTCCA CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40542513..40542690 26863196 MeRIP-seq:(Medium) rs1160593100 Functional Loss DEL dbSNP153 33..33 33 - - - 108810 RMVar_ID_108810 Human_SNP_ID_624134673 m1A Human chr17 - 40542540 40542540 40542540 CTTGAACCTCCCTAAGGGAGGCCTGGGGGGTTAGGGGGGAGTGGAAGGACGGGGGCTCATTTCCA CTTGAACCTCCCTAAGGGAGGCCTGGGGGGTTGGGGGGGAGTGGAAGGACGGGGGCTCATTTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40542513..40542690 26863196 MeRIP-seq:(Medium) rs9675333 Functional Loss SNV dbSNP153 33..33 33 - - - 108811 RMVar_ID_108811 Human_SNP_ID_624154975 m1A Human chr17 - 40630835 40630835 40630835 GCAGAGGAACAGGCCCGCAAAAGGCAGGAGGAAAGGGAGAAGGAGGCCGCAGAGCAAGCTGAGCG GCAGAGGAACAGGCCCGCAAAAGGCAGGAGGACAGGGAGAAGGAGGCCGCAGAGCAAGCTGAGCG T G SMARCE1,AC073508.2 Ensembl:ENSG00000073584,Ensembl:ENSG00000264058 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:40630738..40630900 26863196 MeRIP-seq:(Medium) rs760713355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819938,Human_RBP_ID_26331785 Human_Splice_Rec_1814690,Human_Splice_Rec_1814706,Human_Splice_Rec_1814722,Human_Splice_Rec_1814738,Human_Splice_Rec_1814754,Human_Splice_Rec_1814772,Human_Splice_Rec_1814792,Human_Splice_Rec_1814826,Human_Splice_Rec_1814848,Human_Splice_Rec_1814864,Human_Splice_Rec_1814888,Human_Splice_Rec_1814916,Human_Splice_Rec_1814932,Human_Splice_Rec_1814948,Human_Splice_Rec_1814966,Human_Splice_Rec_1814990,Human_Splice_Rec_1815008,Human_Splice_Rec_1815024,Human_Splice_Rec_1815044,Human_Splice_Rec_1815052,Human_Splice_Rec_1815066,Human_Splice_Rec_1815100,Human_Splice_Rec_1815118,Human_Splice_Rec_1815148,Human_Splice_Rec_1815164,Human_Splice_Rec_1815182,Human_Splice_Rec_1815186,Human_Splice_Rec_1815202,Human_Splice_Rec_1815218,Human_Splice_Rec_1815238,Human_Splice_Rec_1815254,Human_Splice_Rec_1815388,Human_Splice_Rec_1815412 RMVar_hsa_circ_363531 108812 RMVar_ID_108812 Human_SNP_ID_624158322 m1A Human chr17 - 40645849 40645849 40645849 TTCTCTTTTTTTTTTCCTTTTTTTTTTATTTTAGTGTCTCAGATTCATTCTTAAGGAACTGAGAA TTCTCTTTTTTTTTTCCTTTTTTTTTTATTTTTGTGTCTCAGATTCATTCTTAAGGAACTGAGAA T A SMARCE1,AC073508.2 Ensembl:ENSG00000073584,Ensembl:ENSG00000264058 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40645598..40647479 26863196 MeRIP-seq:(Medium) rs1377199841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50295,Human_RBP_ID_6593483,Human_RBP_ID_26331791 Human_Splice_Rec_1814675,Human_Splice_Rec_1814695,Human_Splice_Rec_1814711,Human_Splice_Rec_1814727,Human_Splice_Rec_1814741,Human_Splice_Rec_1814759,Human_Splice_Rec_1814777,Human_Splice_Rec_1814799,Human_Splice_Rec_1814813,Human_Splice_Rec_1814831,Human_Splice_Rec_1814853,Human_Splice_Rec_1814871,Human_Splice_Rec_1814893,Human_Splice_Rec_1814905,Human_Splice_Rec_1814921,Human_Splice_Rec_1814953,Human_Splice_Rec_1814975,Human_Splice_Rec_1814995,Human_Splice_Rec_1815013,Human_Splice_Rec_1815029,Human_Splice_Rec_1815057,Human_Splice_Rec_1815071,Human_Splice_Rec_1815087,Human_Splice_Rec_1815123,Human_Splice_Rec_1815153,Human_Splice_Rec_1815167,Human_Splice_Rec_1815189,Human_Splice_Rec_1815203,Human_Splice_Rec_1815221,Human_Splice_Rec_1815257,Human_Splice_Rec_1815277,Human_Splice_Rec_1815285,Human_Splice_Rec_1815295,Human_Splice_Rec_1815319,Human_Splice_Rec_1815331,Human_Splice_Rec_1815339,Human_Splice_Rec_1815349,Human_Splice_Rec_1815357,Human_Splice_Rec_1815363,Human_Splice_Rec_1815375 108813 RMVar_ID_108813 Human_SNP_ID_624158879 m1A Human chr17 + 40648097 40648097 40648097 GGCCCGACCTAACACAGAATAGGCCTGGGTTTAGCGGCTGTGAGGAGCCGGAGCCGCCGCAGCGA GGCCCGACCTAACACAGAATAGGCCTGGGTTTCGCGGCTGTGAGGAGCCGGAGCCGCCGCAGCGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40648047..40648297 26863196 MeRIP-seq:(Medium) rs1318914326 Functional Loss SNV dbSNP153 33..33 33 - - - 108814 RMVar_ID_108814 Human_SNP_ID_624200832 m1A Human chr17 - 40818484 40818484 40818484 ACTGTTTAAAATTTTTTTTCCATCATTCACACAGATACTAACAAAACCAGAGTAATCAAGACAAT ACTGTTTAAAATTTTTTTTCCATCATTCACACGGATACTAACAAAACCAGAGTAATCAAGACAAT T C KRT10 Ensembl:ENSG00000186395 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40818451..40818500 26863196 MeRIP-seq:(Medium) rs145243680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108815 RMVar_ID_108815 Human_SNP_ID_624200833 m1A Human chr17 - 40818484 40818484 40818484 ACTGTTTAAAATTTTTTTTCCATCATTCACACAGATACTAACAAAACCAGAGTAATCAAGACAAT ACTGTTTAAAATTTTTTTTCCATCATTCACACCGATACTAACAAAACCAGAGTAATCAAGACAAT T G KRT10 Ensembl:ENSG00000186395 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40818451..40818500 26863196 MeRIP-seq:(Medium) rs145243680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108816 RMVar_ID_108816 Human_SNP_ID_624201011 m1A Human chr17 - 40818884 40818867 40818885 GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC GCGGCTACGGGGGCGGCAGCTCCGGCGGCGG__________________ATACGGCGGCGGCAGC TCCGCCGCCGGAGCTGCTG T KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40818776..40818999 26863410 MeRIP-seq:(Medium) rs766129021 Functional Loss DEL dbSNP153 32..49 33 - - - Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4425768,Human_RBP_ID_5496986,Human_RBP_ID_8941820,Human_RBP_ID_18419596 Human_Splice_Rec_1815551 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108817 RMVar_ID_108817 Human_SNP_ID_624201026 m1A Human chr17 + 40818896 40818881 40818896 GTATCCGCCGCCGGAGCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGC GTATCCGCCGCCGGAGCT_______________GCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGC TGCTGCCGCCGCCGGA T - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:40818712..40819000;chr17:40818326..40819653;chr17:40818776..40819099 26863196 MeRIP-seq:(Medium) rs752563839 Functional Loss DEL dbSNP153 19..33 33 - - - 108818 RMVar_ID_108818 Human_SNP_ID_624201029 m1A Human chr17 + 40818911 40818884 40818911 GCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCAC GCTGCT___________________________GCCGCCGCCGCCGCCGCCGGAACTGCCACCAC TGCCGCCGCCGGAGCTGCCGCCCCCGTA T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40818824..40818968 26863196 MeRIP-seq:(Medium) rs753460356 Functional Loss DEL dbSNP153 7..33 33 - - - 108819 RMVar_ID_108819 Human_SNP_ID_624201031 m1A Human chr17 - 40818884 40818884 40818884 GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCGGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC T C KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40818776..40818999 26863410 MeRIP-seq:(Medium) rs1426480004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4425768,Human_RBP_ID_5496986,Human_RBP_ID_8941820,Human_RBP_ID_18419596 Human_Splice_Rec_1815551 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108820 RMVar_ID_108820 Human_SNP_ID_624201036 m1A Human chr17 + 40818896 40818886 40818897 GTATCCGCCGCCGGAGCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGC GTATCCGCCGCCGGAGCTGCTGC___________CTGCCGCCCCCGTAGCCGCCGCCGCCGCCGC CCGCCGCCGGAG C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:40818712..40819000;chr17:40818326..40819653;chr17:40818776..40819099 26863196 MeRIP-seq:(Medium) rs747376338 Functional Loss DEL dbSNP153 24..34 33 - - - 108821 RMVar_ID_108821 Human_SNP_ID_624201055 m1A Human chr17 - 40818899 40818899 40818899 CCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGA CCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCGGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGA T C KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:40818776..40819037 26863196 MeRIP-seq:(Medium) rs1217847176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4464537,Human_RBP_ID_8941820,Human_RBP_ID_18419596 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108822 RMVar_ID_108822 Human_SNP_ID_624201056 m1A Human chr17 + 40818911 40818899 40818911 GCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCAC GCTGCTGCCGCCGCCGGAGCT____________GCCGCCGCCGCCGCCGCCGGAACTGCCACCAC TGCCGCCCCCGTA T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40818824..40818968 26863196 MeRIP-seq:(Medium) rs1318330493 Functional Loss DEL dbSNP153 22..33 33 - - - 108823 RMVar_ID_108823 Human_SNP_ID_624201065 m1A Human chr17 + 40818942 40818906 40818942 TAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC _________________________________CCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC CCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCA C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:40818844..40819049 26863410 MeRIP-seq:(Medium) rs771174062 Functional Loss DEL dbSNP153 1..33 33 - - - 108824 RMVar_ID_108824 Human_SNP_ID_624201072 m1A Human chr17 + 40818911 40818911 40818911 GCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCAC GCTGCTGCCGCCGCCGGAGCTGCCGCCCCCGTTGCCGCCGCCGCCGCCGCCGGAACTGCCACCAC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:40818824..40818968 26863196 MeRIP-seq:(Medium) rs1174924701 Functional Loss SNV dbSNP153 33..33 33 - - - 108825 RMVar_ID_108825 Human_SNP_ID_624201106 m1A Human chr17 + 40818939 40818936 40818939 CCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTG CCGTAGCCGCCGCCGCCGCCGCCGGAACTG___CCACCGTAGCCGCCGCTGGAACTGCCGCCGTG GCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:40818355..40819601;chr17:40818776..40819000 26863196 MeRIP-seq:(Medium) rs1374004174 Functional Loss DEL dbSNP153 31..33 33 - - - 108826 RMVar_ID_108826 Human_SNP_ID_624201109 m1A Human chr17 + 40818939 40818939 40818939 CCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTG CCGTAGCCGCCGCCGCCGCCGCCGGAACTGCCGCCACCGTAGCCGCCGCTGGAACTGCCGCCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr17:40818355..40819601;chr17:40818776..40819000 26863196 MeRIP-seq:(Medium) rs1453766403 Functional Loss SNV dbSNP153 33..33 33 - - - 108827 RMVar_ID_108827 Human_SNP_ID_624201110 m1A Human chr17 + 40818942 40818942 40818942 TAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC TAGCCGCCGCCGCCGCCGCCGGAACTGCCACCCCCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:40818844..40819049 26863410 MeRIP-seq:(Medium) rs750666264 Functional Loss SNV dbSNP153 33..33 33 - - - 108828 RMVar_ID_108828 Human_SNP_ID_624201111 m1A Human chr17 + 40818942 40818942 40818942 TAGCCGCCGCCGCCGCCGCCGGAACTGCCACCACCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC TAGCCGCCGCCGCCGCCGCCGGAACTGCCACCGCCGTAGCCGCCGCTGGAACTGCCGCCGTGGCC A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:40818844..40819049 26863410 MeRIP-seq:(Medium) rs750666264 Functional Loss SNV dbSNP153 33..33 33 - - - 108829 RMVar_ID_108829 Human_SNP_ID_624201149 m1A Human chr17 - 40818987 40818987 40818987 GGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAG GGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGGAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAG T C KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:40818898..40818999 26863410 MeRIP-seq:(Medium) rs1313903750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237078,Human_RBP_ID_4425769,Human_RBP_ID_8941821,Human_RBP_ID_18419596 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108830 RMVar_ID_108830 Human_SNP_ID_624201150 m1A Human chr17 - 40818987 40818987 40818987 GGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGAAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAG GGCGGAAGCTCCGGCGGCGGCTACGGGGGCGGCAGCTCCAGCGGCGGCCACGGCGGCAGTTCCAG T G KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:40818898..40818999 26863410 MeRIP-seq:(Medium) rs1313903750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237078,Human_RBP_ID_4425769,Human_RBP_ID_8941821,Human_RBP_ID_18419596 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 108831 RMVar_ID_108831 Human_SNP_ID_624203310 m1A Human chr17 + 40826490 40826490 40826490 AATGTACAGAAGGTCTAATTCTGAACTTTTGGAGTCACTTTAGGGGCTGGGAAGAAGAAGTAGAG AATGTACAGAAGGTCTAATTCTGAACTTTTGGCGTCACTTTAGGGGCTGGGAAGAAGAAGTAGAG A C TMEM99 Ensembl:ENSG00000167920 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40826485..40826630 26863196 MeRIP-seq:(Medium) rs904969895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94562,RMVar_hsa_circ_98187,RMVar_hsa_circ_184103,RMVar_hsa_circ_184104 108832 RMVar_ID_108832 Human_SNP_ID_624390681 m1A Human chr17 + 41518418 41518418 41518418 TGGTTGGGGTCTGCTTCTGGTACCAGTCATGGATCTTCACCTCCAGGTCAGCATTGGCCTCCTCC TGGTTGGGGTCTGCTTCTGGTACCAGTCATGGGTCTTCACCTCCAGGTCAGCATTGGCCTCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:41518323..41518721 26863196 MeRIP-seq:(Medium) rs1284096520 Functional Loss SNV dbSNP153 33..33 33 - - - 108833 RMVar_ID_108833 Human_SNP_ID_624390902 m1A Human chr17 - 41518938 41518938 41518938 TGGCTTTGCTTTAGGGGAGGAGACGAGGTCCCACAACACCCTCTGAAGGGTATATAAGGAGCCCC TGGCTTTGCTTTAGGGGAGGAGACGAGGTCCCTCAACACCCTCTGAAGGGTATATAAGGAGCCCC T A KRT15 Ensembl:ENSG00000171346 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:41518832..41518996;chr17:41518863..41518963 26863196 MeRIP-seq:(Medium) rs1055348629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1816064 RMVar_hsa_circ_124971,RMVar_hsa_circ_184114 108834 RMVar_ID_108834 Human_SNP_ID_624403229 m1A Human chr17 - 41567668 41567668 41567668 GAGGCAGTTATGGAAGAGGATCCAGGGGAGGAAGTGGAGGCAGCTATGGTGGAGGAGGAAGTGGA GAGGCAGTTATGGAAGAGGATCCAGGGGAGGAGGTGGAGGCAGCTATGGTGGAGGAGGAAGTGGA T C KRT9 Ensembl:ENSG00000171403 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:41567622..41567708 26863196 MeRIP-seq:(Medium) rs1287073782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1816178,Human_Splice_Rec_1816194 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108835 RMVar_ID_108835 Human_SNP_ID_624417980 m1A Human chr17 + 41620528 41620528 41620528 TGCACCCAACCCCCAGGGCCGAAGCCACGCAGATACTTACGTTCTTTCTTGTACTGAGTCAGGCT TGCACCCAACCCCCAGGGCCGAAGCCACGCAGTTACTTACGTTCTTTCTTGTACTGAGTCAGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:41620526..41620575 26863196 MeRIP-seq:(Medium) rs1227678934 Functional Loss SNV dbSNP153 33..33 33 - - - 108836 RMVar_ID_108836 Human_SNP_ID_624418054 m1A Human chr17 - 41620668 41620668 41620668 GATTGCCACCTACCGCCGCCTGCTGGAGGGAGAGGATGCCCAGTGAGTGGGGGCGCCTGGGGTCA GATTGCCACCTACCGCCGCCTGCTGGAGGGAGTGGATGCCCAGTGAGTGGGGGCGCCTGGGGTCA T A KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41619426..41621124 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1816257,Human_Splice_Rec_1816271,Human_Splice_Rec_1816283,Human_Splice_Rec_1816289,Human_Splice_Rec_1816293 RMVar_hsa_circ_85034,RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_105135,RMVar_hsa_circ_118401,RMVar_hsa_circ_119394,RMVar_hsa_circ_83649,RMVar_hsa_circ_88197,RMVar_hsa_circ_184158,RMVar_hsa_circ_184160,RMVar_hsa_circ_184162,RMVar_hsa_circ_184161,RMVar_hsa_circ_184159,RMVar_hsa_circ_120774,RMVar_hsa_circ_184157,RMVar_hsa_circ_88814,RMVar_hsa_circ_114206,RMVar_hsa_circ_184166,RMVar_hsa_circ_184167,RMVar_hsa_circ_184165,RMVar_hsa_circ_184168 108837 RMVar_ID_108837 Human_SNP_ID_624418055 m1A Human chr17 - 41620668 41620668 41620668 GATTGCCACCTACCGCCGCCTGCTGGAGGGAGAGGATGCCCAGTGAGTGGGGGCGCCTGGGGTCA GATTGCCACCTACCGCCGCCTGCTGGAGGGAGGGGATGCCCAGTGAGTGGGGGCGCCTGGGGTCA T C KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41619426..41621124 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1816257,Human_Splice_Rec_1816271,Human_Splice_Rec_1816283,Human_Splice_Rec_1816289,Human_Splice_Rec_1816293 RMVar_hsa_circ_85034,RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_105135,RMVar_hsa_circ_118401,RMVar_hsa_circ_119394,RMVar_hsa_circ_83649,RMVar_hsa_circ_88197,RMVar_hsa_circ_184158,RMVar_hsa_circ_184160,RMVar_hsa_circ_184162,RMVar_hsa_circ_184161,RMVar_hsa_circ_184159,RMVar_hsa_circ_120774,RMVar_hsa_circ_184157,RMVar_hsa_circ_88814,RMVar_hsa_circ_114206,RMVar_hsa_circ_184166,RMVar_hsa_circ_184167,RMVar_hsa_circ_184165,RMVar_hsa_circ_184168 108838 RMVar_ID_108838 Human_SNP_ID_624418084 m1A Human chr17 + 41620741 41620741 41620741 CAGCCGCGTCTTCACATCCAGCAGGATTTTGTATTCCTGGTTCTGCTGCTCCATCTCGCAGCGAA CAGCCGCGTCTTCACATCCAGCAGGATTTTGTGTTCCTGGTTCTGCTGCTCCATCTCGCAGCGAA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:41620598..41620875 26863196 MeRIP-seq:(Medium) rs1451677193 Functional Loss SNV dbSNP153 33..33 33 - - - 108839 RMVar_ID_108839 Human_SNP_ID_624418087 m1A Human chr17 - 41620749 41620749 41620749 GGCCCAGCTTCGCTGCGAGATGGAGCAGCAGAACCAGGAATACAAAATCCTGCTGGATGTGAAGA GGCCCAGCTTCGCTGCGAGATGGAGCAGCAGAGCCAGGAATACAAAATCCTGCTGGATGTGAAGA T C KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41620599..41620822 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_1816257,Human_Splice_Rec_1816271,Human_Splice_Rec_1816283,Human_Splice_Rec_1816289,Human_Splice_Rec_1816293 RMVar_hsa_circ_85034,RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_105135,RMVar_hsa_circ_118401,RMVar_hsa_circ_119394,RMVar_hsa_circ_83649,RMVar_hsa_circ_88197,RMVar_hsa_circ_184158,RMVar_hsa_circ_184160,RMVar_hsa_circ_184162,RMVar_hsa_circ_184161,RMVar_hsa_circ_184159,RMVar_hsa_circ_120774,RMVar_hsa_circ_184157,RMVar_hsa_circ_88814,RMVar_hsa_circ_114206,RMVar_hsa_circ_184166,RMVar_hsa_circ_184167,RMVar_hsa_circ_184165,RMVar_hsa_circ_184168 108840 RMVar_ID_108840 Human_SNP_ID_624418214 m1A Human chr17 - 41621089 41621086 41621090 ACACCGCCCTGTCCTGTGTCCTGTCTGCAGACAGAGGAACTGAACCGCGAGGTGGCCACCAACAG ACACCGCCCTGTCCTGTGTCCTGTCTGCAGA____GGAACTGAACCGCGAGGTGGCCACCAACAG CTCTG C KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41620986..41621124 26863196 MeRIP-seq:(Medium) rs755444195 Functional Loss DEL dbSNP153 32..35 33 - - - Human_Splice_Rec_1816254,Human_Splice_Rec_1816268,Human_Splice_Rec_1816280,Human_Splice_Rec_1816302 RMVar_hsa_circ_85034,RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_105135,RMVar_hsa_circ_119394,RMVar_hsa_circ_83649,RMVar_hsa_circ_88197,RMVar_hsa_circ_184158,RMVar_hsa_circ_184160,RMVar_hsa_circ_184161,RMVar_hsa_circ_184159,RMVar_hsa_circ_120774,RMVar_hsa_circ_184157,RMVar_hsa_circ_88814,RMVar_hsa_circ_76624,RMVar_hsa_circ_114206,RMVar_hsa_circ_184166,RMVar_hsa_circ_184167,RMVar_hsa_circ_184165,RMVar_hsa_circ_103945,RMVar_hsa_circ_184168,RMVar_hsa_circ_184170,RMVar_hsa_circ_20099,RMVar_hsa_circ_184169 108841 RMVar_ID_108841 Human_SNP_ID_624418406 m1A Human chr17 + 41621698 41621698 41621698 TTGAGGATGCGGCTCAGGTCCACGCCTGGGGCAGCGTCCATCTCCACATTGATCTCACCACCCAC TTGAGGATGCGGCTCAGGTCCACGCCTGGGGCCGCGTCCATCTCCACATTGATCTCACCACCCAC A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:41621651..41621775 26863196 MeRIP-seq:(Medium) rs150297631 Functional Loss SNV dbSNP153 33..33 33 - - - 108842 RMVar_ID_108842 Human_SNP_ID_624418407 m1A Human chr17 + 41621698 41621698 41621698 TTGAGGATGCGGCTCAGGTCCACGCCTGGGGCAGCGTCCATCTCCACATTGATCTCACCACCCAC TTGAGGATGCGGCTCAGGTCCACGCCTGGGGCGGCGTCCATCTCCACATTGATCTCACCACCCAC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:41621651..41621775 26863196 MeRIP-seq:(Medium) rs150297631 Functional Loss SNV dbSNP153 33..33 33 - - - 108843 RMVar_ID_108843 Human_SNP_ID_624418416 m1A Human chr17 + 41621722 41621722 41621722 CCTGGGGCAGCGTCCATCTCCACATTGATCTCACCACCCACCTGGCCTCGCAGGGCGTTCATCTC CCTGGGGCAGCGTCCATCTCCACATTGATCTCGCCACCCACCTGGCCTCGCAGGGCGTTCATCTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:41621676..41621750 26863196 MeRIP-seq:(Medium) rs779021627 Functional Loss SNV dbSNP153 33..33 33 - - - 108844 RMVar_ID_108844 Human_SNP_ID_624418786 m1A Human chr17 + 41622989 41622989 41622989 GGAAGTCATCAGCAGCCAGACGGGCATTGTCAATCTGTAGCAGGATGTTGGCATTGTCCACGGTG GGAAGTCATCAGCAGCCAGACGGGCATTGTCAGTCTGTAGCAGGATGTTGGCATTGTCCACGGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:41622951..41623072 26863196 MeRIP-seq:(Medium) rs191021601 Functional Loss SNV dbSNP153 33..33 33 - - - 108845 RMVar_ID_108845 Human_SNP_ID_624419139 m1A Human chr17 - 41624185 41624185 41624185 ACCTGGACAAGGTGCGTGCCCTGGAGGAGGCCAACACTGAGCTGGAGGTGAAGATCCGTGACTGG ACCTGGACAAGGTGCGTGCCCTGGAGGAGGCCGACACTGAGCTGGAGGTGAAGATCCGTGACTGG T C KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41624176..41624225 26863196 MeRIP-seq:(Medium) rs267607412 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15222,GWAS_ID_15223 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_184157,RMVar_hsa_circ_25897,RMVar_hsa_circ_76624,RMVar_hsa_circ_184170 108846 RMVar_ID_108846 Human_SNP_ID_624419184 m1A Human chr17 + 41624267 41624267 41624267 TTGAGGTTCTGCATGGTGGCCTTCTCACCTCCAGCCAGCAGCCCATCAACACCCCCAAAGCTGCT TTGAGGTTCTGCATGGTGGCCTTCTCACCTCCGGCCAGCAGCCCATCAACACCCCCAAAGCTGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr17:41624251..41624275;chr17:41624076..41624743 26863196 MeRIP-seq:(Medium) rs749359456 Functional Loss SNV dbSNP153 33..33 33 - - - 108847 RMVar_ID_108847 Human_SNP_ID_624419274 m1A Human chr17 + 41624402 41624402 41624402 CCGCCAGCAGATCCCAGCCTGCAGGAGCCGGCACCCAGGCCGCCAGACAGCCGGCAGGAGGTGCG CCGCCAGCAGATCCCAGCCTGCAGGAGCCGGCCCCCAGGCCGCCAGACAGCCGGCAGGAGGTGCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:41624351..41624490 26863196 MeRIP-seq:(Medium) rs754000754 Functional Loss SNV dbSNP153 33..33 33 - - - 108848 RMVar_ID_108848 Human_SNP_ID_624419291 m1A Human chr17 + 41624425 41624425 41624425 GGAGCCGGCACCCAGGCCGCCAGACAGCCGGCAGGAGGTGCGGGACGAGCCGCCCCCCAGGCCGG GGAGCCGGCACCCAGGCCGCCAGACAGCCGGCGGGAGGTGCGGGACGAGCCGCCCCCCAGGCCGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:41624376..41624450 26863196 MeRIP-seq:(Medium) rs371000502 Functional Loss SNV dbSNP153 33..33 33 - - - 108849 RMVar_ID_108849 Human_SNP_ID_624436158 m1A Human chr17 - 41688944 41688944 41688944 AGAAGGCGGGCAGGGGGGAACGGAACGTCGGGAAGCGAGGGGGCTCAAGGGGGAGGCTGCTGAAT AGAAGGCGGGCAGGGGGGAACGGAACGTCGGGCAGCGAGGGGGCTCAAGGGGGAGGCTGCTGAAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:41688876..41689431;chr17:41688876..41689173;chr17:41688876..41689346;chr17:41688876..41689075 26863196 MeRIP-seq:(Medium) rs1343297286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108850 RMVar_ID_108850 Human_SNP_ID_624436187 m1A Human chr17 + 41688983 41688976 41688983 GTTCCGTTCCCCCCTGCCCGCCTTCTCCCGCCACCGCCGCCGCCGCCTTCCGCAGGCCGTTTCCA GTTCCGTTCCCCCCTGCCCGCCTTCT_______CCGCCGCCGCCGCCTTCCGCAGGCCGTTTCCA TCCCGCCA T EIF1 Ensembl:ENSG00000173812 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr17:41688876..41689100;chr17:41688884..41689075 26863410 MeRIP-seq:(Medium) rs1249911289 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_236754,Human_RBP_ID_489045,Human_RBP_ID_766176,Human_RBP_ID_821723,Human_RBP_ID_902705,Human_RBP_ID_1857884,Human_RBP_ID_5441425,Human_RBP_ID_5466469,Human_RBP_ID_5497003,Human_RBP_ID_8253420,Human_RBP_ID_9326617,Human_RBP_ID_13001671,Human_RBP_ID_17378338,Human_RBP_ID_17491195,Human_RBP_ID_17692013,Human_RBP_ID_18697416,Human_RBP_ID_18943157,Human_RBP_ID_22532894,Human_RBP_ID_22804365,Human_RBP_ID_23725824,Human_RBP_ID_26460528,Human_RBP_ID_26960720,Human_RBP_ID_27253827,Human_RBP_ID_27452073 Human_Splice_Rec_1816369,Human_Splice_Rec_1816375,Human_Splice_Rec_1816383,Human_Splice_Rec_1816387 RMVar_hsa_circ_116153,RMVar_hsa_circ_184175 108851 RMVar_ID_108851 Human_SNP_ID_624436188 m1A Human chr17 - 41688976 41688976 41688976 GGCCTGCGGAAGGCGGCGGCGGCGGTGGCGGGAGAAGGCGGGCAGGGGGGAACGGAACGTCGGGA GGCCTGCGGAAGGCGGCGGCGGCGGTGGCGGGGGAAGGCGGGCAGGGGGGAACGGAACGTCGGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr17:41688876..41689083;chr17:41688876..41689075 26863196,26863410 MeRIP-seq:(Medium) rs1468457257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108852 RMVar_ID_108852 Human_SNP_ID_624436206 m1A Human chr17 - 41688998 41688998 41688998 ATTCCTTTTCCTCGGTGGAAACGGCCTGCGGAAGGCGGCGGCGGCGGTGGCGGGAGAAGGCGGGC ATTCCTTTTCCTCGGTGGAAACGGCCTGCGGACGGCGGCGGCGGCGGTGGCGGGAGAAGGCGGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,ALKBH3 KO;HEK293T,H2O2 treatment chr17:41688876..41689133;chr17:41688901..41689075 26863410 MeRIP-seq:(Medium) rs928798590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_135214 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108853 RMVar_ID_108853 Human_SNP_ID_624436491 m1A Human chr17 - 41689555 41689553 41689556 GGGAACGCCCGGGCCTCCCGCCCTCCCTGGGAAGCCGATCACATGTCGGGGGAGTCCGGGCTGCC GGGAACGCCCGGGCCTCCCGCCCTCCCTGGG___CCGATCACATGTCGGGGGAGTCCGGGCTGCC GCTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41689529..41689629 26863196 MeRIP-seq:(Medium) rs1207780160 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108854 RMVar_ID_108854 Human_SNP_ID_624436493 m1A Human chr17 - 41689555 41689555 41689555 GGGAACGCCCGGGCCTCCCGCCCTCCCTGGGAAGCCGATCACATGTCGGGGGAGTCCGGGCTGCC GGGAACGCCCGGGCCTCCCGCCCTCCCTGGGAGGCCGATCACATGTCGGGGGAGTCCGGGCTGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41689529..41689629 26863196 MeRIP-seq:(Medium) rs1353420747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108855 RMVar_ID_108855 Human_SNP_ID_624436633 m1A Human chr17 - 41689943 41689943 41689943 TTATGACTTTCCCAAAATCTCACTGAAGACCTACTTTCTTAAACGCCTTCACTAGTTTCTTTTTA TTATGACTTTCCCAAAATCTCACTGAAGACCTTCTTTCTTAAACGCCTTCACTAGTTTCTTTTTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41689918..41689991 26863196 MeRIP-seq:(Medium) rs879138357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108856 RMVar_ID_108856 Human_SNP_ID_624437197 m1A Human chr17 - 41691376 41691375 41691377 ACATCCCTTAGCTAGGATATGTCTGGTCGAACAGACCTTTGTGGCAAGCCAGATGTCCTATCACC ACATCCCTTAGCTAGGATATGTCTGGTCGAA__GACCTTTGTGGCAAGCCAGATGTCCTATCACC CTG C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41691326..41691375 32194978 MeRIP-seq:(Medium) rs1567767353 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 108857 RMVar_ID_108857 Human_SNP_ID_624455479 m1A Human chr17 + 41754800 41754800 41754800 AGCCCCTCACCACACACCAGAGGGGTCAGCCAAGAGCACTTCTCGGGGTCAGCTAGGGCAGCTGT AGCCCCTCACCACACACCAGAGGGGTCAGCCAGGAGCACTTCTCGGGGTCAGCTAGGGCAGCTGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41754751..41754800 26863196 MeRIP-seq:(Medium) rs1201317693 Functional Loss SNV dbSNP153 33..33 33 - - - 108858 RMVar_ID_108858 Human_SNP_ID_624455506 m1A Human chr17 - 41754945 41754945 41754945 AGGGGAGATGGGGAGGAGATATGGAGTGAGTCACCTGCTCCAGAAGATGCCAGCTTCTCTCTCCA AGGGGAGATGGGGAGGAGATATGGAGTGAGTCTCCTGCTCCAGAAGATGCCAGCTTCTCTCTCCA T A JUP Ensembl:ENSG00000173801 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:41754741..41754975 26863196 MeRIP-seq:(Medium) rs936596217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489143,Human_RBP_ID_8191965,Human_RBP_ID_26457532 Human_miRNA_ID_250972,Human_miRNA_ID_2793570,Human_miRNA_ID_2793571,Human_miRNA_ID_2793572 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_77306,RMVar_hsa_circ_96296,RMVar_hsa_circ_104555,RMVar_hsa_circ_121896,RMVar_hsa_circ_125574,RMVar_hsa_circ_107358,RMVar_hsa_circ_97267,RMVar_hsa_circ_89063,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184182,RMVar_hsa_circ_184184,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_184185,RMVar_hsa_circ_184183,RMVar_hsa_circ_184180,RMVar_hsa_circ_184181,RMVar_hsa_circ_184179 108859 RMVar_ID_108859 Human_SNP_ID_624455559 m1A Human chr17 - 41755172 41755172 41755172 GACTCAAGTACCCATTCTGTTTTCCCCCAGCAACGCCCCTCCAAACCTCCAGCCTCCCTGTCTCC GACTCAAGTACCCATTCTGTTTTCCCCCAGCACCGCCCCTCCAAACCTCCAGCCTCCCTGTCTCC T G JUP Ensembl:ENSG00000173801 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41755025..41755247 26863196 MeRIP-seq:(Medium) rs1181334984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8191063,Human_RBP_ID_17378355,Human_RBP_ID_17494926,Human_RBP_ID_17654687,Human_RBP_ID_18941690,Human_RBP_ID_26457535,Human_RBP_ID_26781607 Human_miRNA_ID_1807900,Human_miRNA_ID_2390993,Human_miRNA_ID_2390994,Human_miRNA_ID_2390995,Human_miRNA_ID_2592238,Human_miRNA_ID_2592239,Human_miRNA_ID_2592240,Human_miRNA_ID_2690774,Human_miRNA_ID_2690775,Human_miRNA_ID_2690776 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_77306,RMVar_hsa_circ_96296,RMVar_hsa_circ_104555,RMVar_hsa_circ_121896,RMVar_hsa_circ_125574,RMVar_hsa_circ_107358,RMVar_hsa_circ_97267,RMVar_hsa_circ_89063,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184182,RMVar_hsa_circ_184184,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_184185,RMVar_hsa_circ_184183,RMVar_hsa_circ_184180,RMVar_hsa_circ_184181,RMVar_hsa_circ_184179 108860 RMVar_ID_108860 Human_SNP_ID_624455741 m1A Human chr17 - 41755806 41755806 41755806 AGATGCACATGGACATGGATGGAGACTACCCCATCGACACCTACAGCGACGGCCTCAGGCCCCCG AGATGCACATGGACATGGATGGAGACTACCCCGTCGACACCTACAGCGACGGCCTCAGGCCCCCG T C JUP Ensembl:ENSG00000173801 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41755701..41755835 26863196 MeRIP-seq:(Medium) rs1555597438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49135,Human_RBP_ID_8452201,Human_RBP_ID_22442926 Human_Splice_Rec_1816512,Human_Splice_Rec_1816513,Human_Splice_Rec_1816540,Human_Splice_Rec_1816541,Human_Splice_Rec_1816568 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_116896,RMVar_hsa_circ_77306,RMVar_hsa_circ_96296,RMVar_hsa_circ_121896,RMVar_hsa_circ_125574,RMVar_hsa_circ_107358,RMVar_hsa_circ_97267,RMVar_hsa_circ_89063,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184182,RMVar_hsa_circ_184184,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_184185,RMVar_hsa_circ_184183,RMVar_hsa_circ_184180,RMVar_hsa_circ_184181,RMVar_hsa_circ_375118,RMVar_hsa_circ_184189,RMVar_hsa_circ_184190 108861 RMVar_ID_108861 Human_SNP_ID_624455773 m1A Human chr17 - 41755884 41755884 41755884 AGCCCCACTTTTTGTCCCCAGACATGGATGCCACCTACCGCCCCATGTACTCCAGCGATGTGCCC AGCCCCACTTTTTGTCCCCAGACATGGATGCCGCCTACCGCCCCATGTACTCCAGCGATGTGCCC T C JUP Ensembl:ENSG00000173801 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:41755626..41755900 26863196 MeRIP-seq:(Medium) rs1555597540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903489,Human_RBP_ID_8825477,Human_RBP_ID_9289059,Human_RBP_ID_17892095,Human_RBP_ID_20213449,Human_RBP_ID_22442927 Human_Splice_Rec_1816512,Human_Splice_Rec_1816540,Human_Splice_Rec_1816568 Human_miRNA_ID_2387237,Human_miRNA_ID_2387238,Human_miRNA_ID_2387239,Human_miRNA_ID_2388710,Human_miRNA_ID_2388711,Human_miRNA_ID_2388712,Human_miRNA_ID_2399859,Human_miRNA_ID_2399860,Human_miRNA_ID_2399861,Human_miRNA_ID_3030917,Human_miRNA_ID_3030918,Human_miRNA_ID_3030919 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_116896,RMVar_hsa_circ_77306,RMVar_hsa_circ_96296,RMVar_hsa_circ_121896,RMVar_hsa_circ_125574,RMVar_hsa_circ_107358,RMVar_hsa_circ_97267,RMVar_hsa_circ_89063,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184182,RMVar_hsa_circ_184184,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_184185,RMVar_hsa_circ_184183,RMVar_hsa_circ_184180,RMVar_hsa_circ_184181,RMVar_hsa_circ_375118,RMVar_hsa_circ_184189,RMVar_hsa_circ_184190 108862 RMVar_ID_108862 Human_SNP_ID_624456258 m1A Human chr17 - 41757437 41757437 41757437 GTCCGTGGAGCTCACCAACTCCCTCTTCAAGCATGACCCGGCTGCCTGGGAGGCTGTGAGTATCC GTCCGTGGAGCTCACCAACTCCCTCTTCAAGCGTGACCCGGCTGCCTGGGAGGCTGTGAGTATCC T C JUP Ensembl:ENSG00000173801 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:41757426..41757450 26863196 MeRIP-seq:(Medium) rs539675436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8825478,Human_RBP_ID_22442928 Human_Splice_Rec_1816508,Human_Splice_Rec_1816509,Human_Splice_Rec_1816536,Human_Splice_Rec_1816537,Human_Splice_Rec_1816564,Human_Splice_Rec_1816565 RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_116896,RMVar_hsa_circ_77306,RMVar_hsa_circ_96296,RMVar_hsa_circ_121896,RMVar_hsa_circ_125574,RMVar_hsa_circ_107358,RMVar_hsa_circ_97267,RMVar_hsa_circ_89063,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184182,RMVar_hsa_circ_184184,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_184185,RMVar_hsa_circ_184183,RMVar_hsa_circ_184180,RMVar_hsa_circ_184181,RMVar_hsa_circ_99804,RMVar_hsa_circ_184189,RMVar_hsa_circ_184191,RMVar_hsa_circ_87539,RMVar_hsa_circ_333057,RMVar_hsa_circ_184192,RMVar_hsa_circ_184193 108863 RMVar_ID_108863 Human_SNP_ID_624460064 m1A Human chr17 + 41769513 41769513 41769513 GTCCTGGTAGTTGATGAGATGCACAATGGCCGACTTGAGCAGCTGGGACGGCTCGGCCAGTCGCT GTCCTGGTAGTTGATGAGATGCACAATGGCCGGCTTGAGCAGCTGGGACGGCTCGGCCAGTCGCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:41769501..41769525 26863196 MeRIP-seq:(Medium) rs782755546 Functional Loss SNV dbSNP153 33..33 33 - - - 108864 RMVar_ID_108864 Human_SNP_ID_624460146 m1A Human chr17 + 41769676 41769676 41769676 CTGGCTGTTGTGGACATCTGGTACTCCAGATCACCTGGGGGCCATGGGGACAGGGACTGAGTGCA CTGGCTGTTGTGGACATCTGGTACTCCAGATCGCCTGGGGGCCATGGGGACAGGGACTGAGTGCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr17:41769626..41769700;chr17:41769651..41769700;chr17:41769015..41771464 26863196,32194978 MeRIP-seq:(Medium) rs782504602 Functional Loss SNV dbSNP153 33..33 33 - - - 108865 RMVar_ID_108865 Human_SNP_ID_624460706 m1A Human chr17 - 41771667 41771666 41771667 GTACACGCTCAAGAAAACCACCACTTACACCCAGGGGGTGCCCCCCAGCCAAGGTCAGGACCCCT GTACACGCTCAAGAAAACCACCACTTACACCC_GGGGGTGCCCCCCAGCCAAGGTCAGGACCCCT CT C JUP Ensembl:ENSG00000173801 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41771662..41772243 32194978 MeRIP-seq:(Medium) rs1555606936 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_820276,Human_RBP_ID_22444543 Human_Splice_Rec_1816489,Human_Splice_Rec_1816517,Human_Splice_Rec_1816545,Human_Splice_Rec_1816575,Human_Splice_Rec_1816583,Human_Splice_Rec_1816591,Human_Splice_Rec_1816601,Human_Splice_Rec_1816607,Human_Splice_Rec_1816613 Human_miRNA_ID_1357559,Human_miRNA_ID_2218532,Human_miRNA_ID_2218533,Human_miRNA_ID_2218534,Human_miRNA_ID_2437101,Human_miRNA_ID_2437102,Human_miRNA_ID_2437103,Human_miRNA_ID_2660514,Human_miRNA_ID_2660515,Human_miRNA_ID_2660516,Human_miRNA_ID_2685786,Human_miRNA_ID_2685787,Human_miRNA_ID_2685788 Clinvar_Rec_701 RMVar_hsa_circ_117561,RMVar_hsa_circ_107266,RMVar_hsa_circ_184129,RMVar_hsa_circ_184130,RMVar_hsa_circ_116896,RMVar_hsa_circ_121896,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_36432,RMVar_hsa_circ_184189,RMVar_hsa_circ_365901,RMVar_hsa_circ_81477,RMVar_hsa_circ_184202,RMVar_hsa_circ_92802,RMVar_hsa_circ_184203 108866 RMVar_ID_108866 Human_SNP_ID_624460781 m1A Human chr17 - 41771850 41771850 41771850 TTCCTCCTTTGTGCCCCCAGTAGCCACGATGGAGGTGATGAACCTGATGGAGCAGCCTATCAAGG TTCCTCCTTTGTGCCCCCAGTAGCCACGATGGGGGTGATGAACCTGATGGAGCAGCCTATCAAGG T C JUP Ensembl:ENSG00000173801 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:41771613..41771956;chr17:41771801..41771875 26863196 MeRIP-seq:(Medium) rs112065669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49145,Human_RBP_ID_1533653,Human_RBP_ID_1857914,Human_RBP_ID_4465376,Human_RBP_ID_22656252 Human_Splice_Rec_1816488,Human_Splice_Rec_1816516,Human_Splice_Rec_1816544,Human_Splice_Rec_1816574,Human_Splice_Rec_1816582,Human_Splice_Rec_1816590,Human_Splice_Rec_1816600,Human_Splice_Rec_1816606,Human_Splice_Rec_1816612,Human_Splice_Rec_1816616,Human_Splice_Rec_1816620 Human_miRNA_ID_2016899,Human_miRNA_ID_2016900,Human_miRNA_ID_2016901,Human_miRNA_ID_2016902 RMVar_hsa_circ_117561,RMVar_hsa_circ_107266,RMVar_hsa_circ_184129,RMVar_hsa_circ_184130,RMVar_hsa_circ_116896,RMVar_hsa_circ_121896,RMVar_hsa_circ_89844,RMVar_hsa_circ_86967,RMVar_hsa_circ_184186,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188,RMVar_hsa_circ_36432,RMVar_hsa_circ_184189,RMVar_hsa_circ_365901,RMVar_hsa_circ_81477,RMVar_hsa_circ_184202,RMVar_hsa_circ_92802,RMVar_hsa_circ_184203 108867 RMVar_ID_108867 Human_SNP_ID_624464883 m1A Human chr17 - 41786667 41786667 41786667 TGGCCAGAGTCCGGAGCAGCCGCCGCCCGACCACGCCGAGCTCAGTTCGCTGTCCGCGCCGGCTC TGGCCAGAGTCCGGAGCAGCCGCCGCCCGACCGCGCCGAGCTCAGTTCGCTGTCCGCGCCGGCTC T C JUP Ensembl:ENSG00000173801 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:41786505..41786725;chr17:41786513..41786700;chr17:41786286..41786725 26863196 MeRIP-seq:(Medium) rs4796702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236753,Human_RBP_ID_821168,Human_RBP_ID_4465379,Human_RBP_ID_8825489,Human_RBP_ID_9289068,Human_RBP_ID_9326627,Human_RBP_ID_22532898,Human_RBP_ID_22588066 Human_Splice_Rec_1816515,Human_Splice_Rec_1816543,Human_Splice_Rec_1816597,Human_Splice_Rec_1816615 Clinvar_Rec_702 GWAS_ID_15224,GWAS_ID_15225 RMVar_hsa_circ_121896,RMVar_hsa_circ_184188 108868 RMVar_ID_108868 Human_SNP_ID_624464884 m1A Human chr17 - 41786667 41786667 41786667 TGGCCAGAGTCCGGAGCAGCCGCCGCCCGACCACGCCGAGCTCAGTTCGCTGTCCGCGCCGGCTC TGGCCAGAGTCCGGAGCAGCCGCCGCCCGACCCCGCCGAGCTCAGTTCGCTGTCCGCGCCGGCTC T G JUP Ensembl:ENSG00000173801 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr17:41786505..41786725;chr17:41786513..41786700;chr17:41786286..41786725 26863196 MeRIP-seq:(Medium) rs4796702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236753,Human_RBP_ID_821168,Human_RBP_ID_4465379,Human_RBP_ID_8825489,Human_RBP_ID_9289068,Human_RBP_ID_9326627,Human_RBP_ID_22532898,Human_RBP_ID_22588066 Human_Splice_Rec_1816515,Human_Splice_Rec_1816543,Human_Splice_Rec_1816597,Human_Splice_Rec_1816615 Clinvar_Rec_702 GWAS_ID_15224,GWAS_ID_15225 RMVar_hsa_circ_121896,RMVar_hsa_circ_184188 108869 RMVar_ID_108869 Human_SNP_ID_624464885 m1A Human chr17 - 41786670 41786670 41786670 CCTTGGCCAGAGTCCGGAGCAGCCGCCGCCCGACCACGCCGAGCTCAGTTCGCTGTCCGCGCCGG CCTTGGCCAGAGTCCGGAGCAGCCGCCGCCCGGCCACGCCGAGCTCAGTTCGCTGTCCGCGCCGG T C JUP Ensembl:ENSG00000173801 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:41786542..41786725 26863196 MeRIP-seq:(Medium) rs1236026459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236753,Human_RBP_ID_821168,Human_RBP_ID_4426145,Human_RBP_ID_8825489,Human_RBP_ID_9289068,Human_RBP_ID_9326627,Human_RBP_ID_22588066 Human_Splice_Rec_1816515,Human_Splice_Rec_1816543,Human_Splice_Rec_1816597,Human_Splice_Rec_1816615 RMVar_hsa_circ_121896,RMVar_hsa_circ_184188 108870 RMVar_ID_108870 Human_SNP_ID_624469061 m1A Human chr17 - 41802560 41802559 41802560 GCGACAGAGCGAGACTCCATCTTTAAAAAAAAACAAGACGGGCCGGCACGGTGGCTCACGCCTGT GCGACAGAGCGAGACTCCATCTTTAAAAAAAA_CAAGACGGGCCGGCACGGTGGCTCACGCCTGT GT G P3H4 Ensembl:ENSG00000141696 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41802509..41802713 26863196 MeRIP-seq:(Medium) rs1172155017 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_489172,Human_RBP_ID_17692022,Human_RBP_ID_17892103,Human_RBP_ID_18292197,Human_RBP_ID_27452119 RMVar_hsa_circ_77359,RMVar_hsa_circ_105661,RMVar_hsa_circ_90167,RMVar_hsa_circ_102394,RMVar_hsa_circ_82902,RMVar_hsa_circ_184204,RMVar_hsa_circ_184206,RMVar_hsa_circ_184207,RMVar_hsa_circ_184208,RMVar_hsa_circ_184205 108871 RMVar_ID_108871 Human_SNP_ID_624470525 m1A Human chr17 - 41807978 41807978 41807978 CTGCAGTGAATGATGTGCGCCAGGCTGCCCGCAGCGCCGCCAGCTACATGCTCTTCGACCCCAAG CTGCAGTGAATGATGTGCGCCAGGCTGCCCGCGGCGCCGCCAGCTACATGCTCTTCGACCCCAAG T C P3H4 Ensembl:ENSG00000141696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:41807933..41808043 26863196 MeRIP-seq:(Medium) rs782189430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236417,Human_RBP_ID_18697487,Human_RBP_ID_23725933 Human_Splice_Rec_1816630,Human_Splice_Rec_1816644,Human_Splice_Rec_1816666 RMVar_hsa_circ_123332,RMVar_hsa_circ_77359,RMVar_hsa_circ_105661,RMVar_hsa_circ_90167,RMVar_hsa_circ_82902,RMVar_hsa_circ_184204,RMVar_hsa_circ_184206,RMVar_hsa_circ_184207,RMVar_hsa_circ_184205,RMVar_hsa_circ_61003,RMVar_hsa_circ_184210 108872 RMVar_ID_108872 Human_SNP_ID_624470841 m1A Human chr17 + 41809537 41809537 41809537 CTGTTCTCACTCAGAAGCCTCTCACCTGCCCCAGACTCCCAGGGTGCCTTCCCCATATTCCCACC CTGTTCTCACTCAGAAGCCTCTCACCTGCCCCGGACTCCCAGGGTGCCTTCCCCATATTCCCACC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41809531..41809695 26863196 MeRIP-seq:(Medium) rs1361275723 Functional Loss SNV dbSNP153 33..33 33 - - - 108873 RMVar_ID_108873 Human_SNP_ID_624471545 m1A Human chr17 + 41811539 41811539 41811539 GCAGCAGCTGCCGCGGCGGGTAGGGCACCTGGAAGGCGGGCAGCGTCCGCTTGCAGCGCCGCAGG GCAGCAGCTGCCGCGGCGGGTAGGGCACCTGGGAGGCGGGCAGCGTCCGCTTGCAGCGCCGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41811223..41811892 32194978 MeRIP-seq:(Medium) rs529456250 Functional Loss SNV dbSNP153 33..33 33 - - - 108874 RMVar_ID_108874 Human_SNP_ID_624471938 m1A Human chr17 + 41812347 41812347 41812347 CCTCCTGCACCCTCCGAGTGTCTCCCCCGCCCACGTCGGAGGCACACACCTGCTGTCACCTGCAC CCTCCTGCACCCTCCGAGTGTCTCCCCCGCCCCCGTCGGAGGCACACACCTGCTGTCACCTGCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:41812297..41812433;chr17:41812297..41812441 26863196 MeRIP-seq:(Medium) rs182344433 Functional Loss SNV dbSNP153 33..33 33 - - - 108875 RMVar_ID_108875 Human_SNP_ID_624472151 m1A Human chr17 - 41813018 41813018 41813018 GGCCCGCGGGGAACATGGTGCCTGGAGTTGGGACCGCCGGCAGTGAGGGCGAGCGAGGGAGTCGC GGCCCGCGGGGAACATGGTGCCTGGAGTTGGGGCCGCCGGCAGTGAGGGCGAGCGAGGGAGTCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:41812756..41813310;chr17:41812969..41813099 26863196 MeRIP-seq:(Medium) rs782788196 Functional Loss SNV dbSNP153 33..33 33 - - - 108876 RMVar_ID_108876 Human_SNP_ID_624472156 m1A Human chr17 - 41813025 41813025 41813025 CTGGGGGGGCCCGCGGGGAACATGGTGCCTGGAGTTGGGACCGCCGGCAGTGAGGGCGAGCGAGG CTGGGGGGGCCCGCGGGGAACATGGTGCCTGGTGTTGGGACCGCCGGCAGTGAGGGCGAGCGAGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41812723..41813113 26863196 MeRIP-seq:(Medium) rs782166587 Functional Loss SNV dbSNP153 33..33 33 - - - 108877 RMVar_ID_108877 Human_SNP_ID_624472157 m1A Human chr17 - 41813025 41813025 41813025 CTGGGGGGGCCCGCGGGGAACATGGTGCCTGGAGTTGGGACCGCCGGCAGTGAGGGCGAGCGAGG CTGGGGGGGCCCGCGGGGAACATGGTGCCTGGCGTTGGGACCGCCGGCAGTGAGGGCGAGCGAGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41812723..41813113 26863196 MeRIP-seq:(Medium) rs782166587 Functional Loss SNV dbSNP153 33..33 33 - - - 108878 RMVar_ID_108878 Human_SNP_ID_624473729 m1A Human chr17 - 41818529 41818529 41818529 CGGAATTTCCCCTTGTGTCCTTGCCCACCCTCACCATAGCCTTTCTCGCCATAGGCCAGGAATGG CGGAATTTCCCCTTGTGTCCTTGCCCACCCTCCCCATAGCCTTTCTCGCCATAGGCCAGGAATGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41818385..41818580 26863196 MeRIP-seq:(Medium) rs113277297 Functional Loss SNV dbSNP153 33..33 33 - - - 108879 RMVar_ID_108879 Human_SNP_ID_624473973 m1A Human chr17 + 41819288 41819288 41819288 GATTGACGTGCACAACCCGAAGGACGCTGTCCAGCTAGAGACGCTGGAGCTCCCCCCCGGCTGTG GATTGACGTGCACAACCCGAAGGACGCTGTCCGGCTAGAGACGCTGGAGCTCCCCCCCGGCTGTG A G FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:41819237..41819383 26863196 MeRIP-seq:(Medium) rs1555616565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489189,Human_RBP_ID_9378146,Human_RBP_ID_18991234,Human_RBP_ID_22761485,Human_RBP_ID_23114465 Human_Splice_Rec_1816702,Human_Splice_Rec_1816720 Human_miRNA_ID_1321764,Human_miRNA_ID_1478359,Human_miRNA_ID_1968824 RMVar_hsa_circ_84051,RMVar_hsa_circ_76713,RMVar_hsa_circ_82162,RMVar_hsa_circ_85112,RMVar_hsa_circ_184214,RMVar_hsa_circ_184215,RMVar_hsa_circ_184216,RMVar_hsa_circ_86165,RMVar_hsa_circ_184217,RMVar_hsa_circ_184218 108880 RMVar_ID_108880 Human_SNP_ID_624474007 m1A Human chr17 + 41819362 41819325 41819362 CCGGGGCCGGGGACTTCATGCGCTACCACTACAATGGCTCCTTGATGGACGGCACCCTCTTCGAT _________________________________ATGGCTCCTTGATGGACGGCACCCTCTTCGAT CAGAGCCGGGGCCGGGGACTTCATGCGCTACCACTACA C FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41819201..41819400 32194978 MeRIP-seq:(Medium) rs1567855092 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_5497013,Human_RBP_ID_26960863 Human_Splice_Rec_1816703,Human_Splice_Rec_1816721,Human_Splice_Rec_1816731,Human_Splice_Rec_1816733 Human_miRNA_ID_291878,Human_miRNA_ID_723558,Human_miRNA_ID_2903088 RMVar_hsa_circ_84051,RMVar_hsa_circ_76713,RMVar_hsa_circ_82162,RMVar_hsa_circ_85112,RMVar_hsa_circ_184214,RMVar_hsa_circ_184215,RMVar_hsa_circ_184216,RMVar_hsa_circ_86165,RMVar_hsa_circ_184217,RMVar_hsa_circ_184218 108881 RMVar_ID_108881 Human_SNP_ID_624474145 m1A Human chr17 + 41819630 41819620 41819630 GGCTGCAGGGTGCCTGCATGGGGGAACGCCGGAGAATTACCATCCCCCCGCACCTCGCCTATGGG GGCTGCAGGGTGCCTGCATGGGG__________GAATTACCATCCCCCCGCACCTCGCCTATGGG GGAACGCCGGA G FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41819580..41819702 26863196 MeRIP-seq:(Medium) rs782351844 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_765688,Human_RBP_ID_18988422,Human_RBP_ID_21974352,Human_RBP_ID_22213686,Human_RBP_ID_22444551,Human_RBP_ID_26960870 Human_Splice_Rec_1816723,Human_Splice_Rec_1816735 Human_miRNA_ID_88383,Human_miRNA_ID_1321765,Human_miRNA_ID_1478360,Human_miRNA_ID_1957568,Human_miRNA_ID_2653566,Human_miRNA_ID_2754764 RMVar_hsa_circ_76713,RMVar_hsa_circ_82162,RMVar_hsa_circ_184215,RMVar_hsa_circ_184216,RMVar_hsa_circ_86165,RMVar_hsa_circ_184217 108882 RMVar_ID_108882 Human_SNP_ID_624474424 m1A Human chr17 + 41820374 41820374 41820374 GGTGGAAATCAGGACACTGTCCCGGCCATCTGAGACCTGCAATGAGACCACCAAGCTTGGGGACT GGTGGAAATCAGGACACTGTCCCGGCCATCTGGGACCTGCAATGAGACCACCAAGCTTGGGGACT A G FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41820221..41820485 26863196 MeRIP-seq:(Medium) rs368314546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1533669,Human_RBP_ID_1857935,Human_RBP_ID_3523060,Human_RBP_ID_9378150,Human_RBP_ID_13002310,Human_RBP_ID_18697505,Human_RBP_ID_23114466,Human_RBP_ID_26330758 Human_Splice_Rec_1816707,Human_Splice_Rec_1816725,Human_Splice_Rec_1816739,Human_Splice_Rec_1816745 RMVar_hsa_circ_76713,RMVar_hsa_circ_184216,RMVar_hsa_circ_86165,RMVar_hsa_circ_184217,RMVar_hsa_circ_106402,RMVar_hsa_circ_184219 108883 RMVar_ID_108883 Human_SNP_ID_624475188 m1A Human chr17 + 41822408 41822406 41822408 GAGGACGAGGAGCGGGTCCACGAGGAGCTCTGAGGGGCAGGGAGCCTGGCCAGGCCTGAGACACA GAGGACGAGGAGCGGGTCCACGAGGAGCTCT__GGGGCAGGGAGCCTGGCCAGGCCTGAGACACA TGA T FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1555617402 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_237942,Human_RBP_ID_767135,Human_RBP_ID_9378160,Human_RBP_ID_13002340,Human_RBP_ID_17892121,Human_RBP_ID_26960904,Human_RBP_ID_27452159 108884 RMVar_ID_108884 Human_SNP_ID_624475205 m1A Human chr17 + 41822440 41822439 41822441 AGGGGCAGGGAGCCTGGCCAGGCCTGAGACACAGAGGCCCACTGCGAGGGGGACAGTGGCGGTGG AGGGGCAGGGAGCCTGGCCAGGCCTGAGACAC__AGGCCCACTGCGAGGGGGACAGTGGCGGTGG CAG C FKBP10 Ensembl:ENSG00000141756 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs782336656 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_489202,Human_RBP_ID_9378160,Human_RBP_ID_27452161 108885 RMVar_ID_108885 Human_SNP_ID_624476205 m1A Human chr17 - 41826442 41826442 41826442 AGGGCAGGGGGATCACTTGAGGCCAGGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCCTGT AGGGCAGGGGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCTGT T C NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs966824715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25282916 108886 RMVar_ID_108886 Human_SNP_ID_624477392 m1A Human chr17 - 41830881 41830880 41830881 TTTTCTGGGGTGTCTGTTTCTAGGTGGACCAAAGCACACAATCTCCTATGTCAGCAGAAGATTCA TTTTCTGGGGTGTCTGTTTCTAGGTGGACCAA_GCACACAATCTCCTATGTCAGCAGAAGATTCA CT C NT5C3B Ensembl:ENSG00000141698 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:41828883..41832432 32194978 MeRIP-seq:(Medium) rs782385849 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9378162,Human_RBP_ID_17262899,Human_RBP_ID_18991240 Human_Splice_Rec_1816764,Human_Splice_Rec_1816765,Human_Splice_Rec_1816772,Human_Splice_Rec_1816773,Human_Splice_Rec_1816788,Human_Splice_Rec_1816789,Human_Splice_Rec_1816802,Human_Splice_Rec_1816803,Human_Splice_Rec_1816816,Human_Splice_Rec_1816817,Human_Splice_Rec_1816828,Human_Splice_Rec_1816829,Human_Splice_Rec_1816842,Human_Splice_Rec_1816843,Human_Splice_Rec_1816870,Human_Splice_Rec_1816871,Human_Splice_Rec_1816882,Human_Splice_Rec_1816883,Human_Splice_Rec_1816887,Human_Splice_Rec_1816900,Human_Splice_Rec_1816901,Human_Splice_Rec_1816904,Human_Splice_Rec_1816905,Human_Splice_Rec_1816918,Human_Splice_Rec_1816919,Human_Splice_Rec_1816928,Human_Splice_Rec_1816929 Human_miRNA_ID_2237595,Human_miRNA_ID_2237596 RMVar_hsa_circ_3939,RMVar_hsa_circ_184224,RMVar_hsa_circ_313187,RMVar_hsa_circ_301754,RMVar_hsa_circ_98425,RMVar_hsa_circ_184223,RMVar_hsa_circ_275264,RMVar_hsa_circ_325560,RMVar_hsa_circ_272642,RMVar_hsa_circ_115280,RMVar_hsa_circ_184226,RMVar_hsa_circ_184227,RMVar_hsa_circ_184225,RMVar_hsa_circ_105889,RMVar_hsa_circ_184228,RMVar_hsa_circ_184229 108887 RMVar_ID_108887 Human_SNP_ID_624478736 m1A Human chr17 + 41835981 41835981 41835981 GGTGCTCACCTGTCCCGAGACCCGAGAGAACCACTGACCCCTGCGCCACGCTGGGCCCGAGGGGA GGTGCTCACCTGTCCCGAGACCCGAGAGAACCCCTGACCCCTGCGCCACGCTGGGCCCGAGGGGA A C KLHL10 Ensembl:ENSG00000161594 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:41835977..41836152 26863196 MeRIP-seq:(Medium) rs1555619938 Functional Loss SNV dbSNP153 33..33 33 - - - 108888 RMVar_ID_108888 Human_SNP_ID_624478814 m1A Human chr17 - 41836175 41836175 41836175 AGGCCTCGAACGGGATGGCAGAGGAGGTGAGGAGGGAGGAAGCGTCCGGAGTGGGGCGGGCCCGG AGGCCTCGAACGGGATGGCAGAGGAGGTGAGGCGGGAGGAAGCGTCCGGAGTGGGGCGGGCCCGG T G NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,untreat control;HEPG2 cell line,mRNA untreated chr17:41836074..41836213;chr17:41835820..41836250 26863410,26863196 MeRIP-seq:(Medium) rs1364449863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237937,Human_RBP_ID_489262,Human_RBP_ID_767124,Human_RBP_ID_4465381,Human_RBP_ID_17669876,Human_RBP_ID_18419597,Human_RBP_ID_18991242,Human_RBP_ID_22959411 108889 RMVar_ID_108889 Human_SNP_ID_624486193 m1A Human chr17 - 41865248 41865248 41865248 GCCGGCTCGGCAGGACTGGCCGCCGAGGTCCGAGGCAGCGGCACGGTGGACTTCGGGCCTGGGCC GCCGGCTCGGCAGGACTGGCCGCCGAGGTCCGCGGCAGCGGCACGGTGGACTTCGGGCCTGGGCC T G KLHL11 Ensembl:ENSG00000178502 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41865200..41865350 26863196 MeRIP-seq:(Medium) rs1274374428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4466409,Human_RBP_ID_8825492 108890 RMVar_ID_108890 Human_SNP_ID_624486212 m1A Human chr17 + 41865274 41865274 41865274 GCTGCCTCGGACCTCGGCGGCCAGTCCTGCCGAGCCGGCGGCGGCCGTCTCCATGCTCTCCATCT GCTGCCTCGGACCTCGGCGGCCAGTCCTGCCGCGCCGGCGGCGGCCGTCTCCATGCTCTCCATCT A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:41865178..41865291 26863196 MeRIP-seq:(Medium) rs1411594753 Functional Loss SNV dbSNP153 33..33 33 - - - 108891 RMVar_ID_108891 Human_SNP_ID_624486260 m1A Human chr17 + 41865362 41865341 41865362 GCGGCCGCCGCCGCCGCCGCCGCCACTGCCGCAGCCGCCATCTTGACGCCGCTGCGCCCGGCCTC GCGGCCGCCGCC_____________________GCCGCCATCTTGACGCCGCTGCGCCCGGCCTC CGCCGCCGCCGCCACTGCCGCA C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:41865126..41865400;chr17:41865122..41865387;chr17:41865105..41865400 26863196 MeRIP-seq:(Medium) rs1351426634 Functional Loss DEL dbSNP153 13..33 33 - - - 108892 RMVar_ID_108892 Human_SNP_ID_624486273 m1A Human chr17 + 41865362 41865362 41865362 GCGGCCGCCGCCGCCGCCGCCGCCACTGCCGCAGCCGCCATCTTGACGCCGCTGCGCCCGGCCTC GCGGCCGCCGCCGCCGCCGCCGCCACTGCCGCCGCCGCCATCTTGACGCCGCTGCGCCCGGCCTC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:41865126..41865400;chr17:41865122..41865387;chr17:41865105..41865400 26863196 MeRIP-seq:(Medium) rs760861374 Functional Loss SNV dbSNP153 33..33 33 - - - 108893 RMVar_ID_108893 Human_SNP_ID_624486280 m1A Human chr17 + 41865375 41865375 41865375 CCGCCGCCGCCACTGCCGCAGCCGCCATCTTGACGCCGCTGCGCCCGGCCTCCACAGCCTCGGAA CCGCCGCCGCCACTGCCGCAGCCGCCATCTTGGCGCCGCTGCGCCCGGCCTCCACAGCCTCGGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41865132..41865406 26863196 MeRIP-seq:(Medium) rs1329751019 Functional Loss SNV dbSNP153 33..33 33 - - - 108894 RMVar_ID_108894 Human_SNP_ID_624488186 m1A Human chr17 + 41872001 41872001 41872001 AAAGCAGCATGAGGCCAAGGCCCAGTGTCCCCACTGTTCACCTCCCATGATGACAGTACTTACGA AAAGCAGCATGAGGCCAAGGCCCAGTGTCCCCCCTGTTCACCTCCCATGATGACAGTACTTACGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41871996..41872173 26863196 MeRIP-seq:(Medium) rs1555625173 Functional Loss SNV dbSNP153 33..33 33 - - - 108895 RMVar_ID_108895 Human_SNP_ID_624492539 m1A Human chr17 - 41887642 41887642 41887642 CATCCCTGAGGCCCTCACGAGAAAGCTGATCAAGAAGGCGGACCAGAAGGGAGTGACCATCATCG CATCCCTGAGGCCCTCACGAGAAAGCTGATCAGGAAGGCGGACCAGAAGGGAGTGACCATCATCG T C ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:41887601..41887725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_47856,Human_RBP_ID_1858056,Human_RBP_ID_4472923,Human_RBP_ID_6594321,Human_RBP_ID_13003227,Human_RBP_ID_18191250,Human_RBP_ID_18991246 Human_Splice_Rec_1816984,Human_Splice_Rec_1816985,Human_Splice_Rec_1817040,Human_Splice_Rec_1817041,Human_Splice_Rec_1817094,Human_Splice_Rec_1817095,Human_Splice_Rec_1817134,Human_Splice_Rec_1817135,Human_Splice_Rec_1817188,Human_Splice_Rec_1817189 RMVar_hsa_circ_12047,RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,RMVar_hsa_circ_328213,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_48177,RMVar_hsa_circ_26428,RMVar_hsa_circ_36797,RMVar_hsa_circ_71828,RMVar_hsa_circ_12315,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_88232,RMVar_hsa_circ_113752,RMVar_hsa_circ_184241,RMVar_hsa_circ_20919,RMVar_hsa_circ_345873,RMVar_hsa_circ_369787,RMVar_hsa_circ_104323,RMVar_hsa_circ_122588,RMVar_hsa_circ_184243,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_184242,RMVar_hsa_circ_280105,RMVar_hsa_circ_184245,RMVar_hsa_circ_184246 108896 RMVar_ID_108896 Human_SNP_ID_624493949 m1A Human chr17 - 41893163 41893163 41893163 CTCTGTGTCTTTGCCCACCAGGAAAGAGCACCACCCTCTTCAGCCGCCACACCAAGGCCATTGTG CTCTGTGTCTTTGCCCACCAGGAAAGAGCACCGCCCTCTTCAGCCGCCACACCAAGGCCATTGTG T C ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41893112..41893220 26863196 MeRIP-seq:(Medium) rs781837455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22213805,Human_RBP_ID_22499435,Human_RBP_ID_22656259 Human_Splice_Rec_1816980,Human_Splice_Rec_1817036,Human_Splice_Rec_1817090,Human_Splice_Rec_1817130,Human_Splice_Rec_1817184 RMVar_hsa_circ_52809,RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_88232,RMVar_hsa_circ_113752,RMVar_hsa_circ_184241,RMVar_hsa_circ_345873,RMVar_hsa_circ_104323,RMVar_hsa_circ_122588,RMVar_hsa_circ_184243,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_184246,RMVar_hsa_circ_337025,RMVar_hsa_circ_371706,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_80190,RMVar_hsa_circ_184247,RMVar_hsa_circ_184249,RMVar_hsa_circ_184251,RMVar_hsa_circ_42132,RMVar_hsa_circ_184252,RMVar_hsa_circ_184250,RMVar_hsa_circ_184248 108897 RMVar_ID_108897 Human_SNP_ID_624493950 m1A Human chr17 - 41893163 41893163 41893163 CTCTGTGTCTTTGCCCACCAGGAAAGAGCACCACCCTCTTCAGCCGCCACACCAAGGCCATTGTG CTCTGTGTCTTTGCCCACCAGGAAAGAGCACCCCCCTCTTCAGCCGCCACACCAAGGCCATTGTG T G ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41893112..41893220 26863196 MeRIP-seq:(Medium) rs781837455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22213805,Human_RBP_ID_22499435,Human_RBP_ID_22656259 Human_Splice_Rec_1816980,Human_Splice_Rec_1817036,Human_Splice_Rec_1817090,Human_Splice_Rec_1817130,Human_Splice_Rec_1817184 RMVar_hsa_circ_52809,RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_88232,RMVar_hsa_circ_113752,RMVar_hsa_circ_184241,RMVar_hsa_circ_345873,RMVar_hsa_circ_104323,RMVar_hsa_circ_122588,RMVar_hsa_circ_184243,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_184246,RMVar_hsa_circ_337025,RMVar_hsa_circ_371706,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_80190,RMVar_hsa_circ_184247,RMVar_hsa_circ_184249,RMVar_hsa_circ_184251,RMVar_hsa_circ_42132,RMVar_hsa_circ_184252,RMVar_hsa_circ_184250,RMVar_hsa_circ_184248 108898 RMVar_ID_108898 Human_SNP_ID_624495356 m1A Human chr17 - 41898777 41898777 41898777 GATTTTTTTTTCCTTCCCTTGCAGGGAAGACCACTGGGATCCCCATCCATGTCTTTGGCACAGAG GATTTTTTTTTCCTTCCCTTGCAGGGAAGACCCCTGGGATCCCCATCCATGTCTTTGGCACAGAG T G ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:41898726..41898800 26863196 MeRIP-seq:(Medium) rs782102822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_902670,Human_RBP_ID_1286347,Human_RBP_ID_1858065,Human_RBP_ID_3952353,Human_RBP_ID_4426784,Human_RBP_ID_8824667,Human_RBP_ID_9289088,Human_RBP_ID_18991250,Human_RBP_ID_22443642 Human_Splice_Rec_1816974,Human_Splice_Rec_1817030,Human_Splice_Rec_1817086,Human_Splice_Rec_1817126,Human_Splice_Rec_1817180,Human_Splice_Rec_1817228 Human_miRNA_ID_2952643 RMVar_hsa_circ_52809,RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_113752,RMVar_hsa_circ_345873,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_371706,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_80190,RMVar_hsa_circ_24463,RMVar_hsa_circ_184247,RMVar_hsa_circ_184249,RMVar_hsa_circ_184251,RMVar_hsa_circ_184250,RMVar_hsa_circ_184248,RMVar_hsa_circ_108758,RMVar_hsa_circ_117742,RMVar_hsa_circ_63838,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_184254,RMVar_hsa_circ_184255,RMVar_hsa_circ_337607,RMVar_hsa_circ_23263,RMVar_hsa_circ_281874,RMVar_hsa_circ_330957,RMVar_hsa_circ_309521,RMVar_hsa_circ_281028,RMVar_hsa_circ_184257,RMVar_hsa_circ_184259,RMVar_hsa_circ_184260,RMVar_hsa_circ_184258 108899 RMVar_ID_108899 Human_SNP_ID_624497060 m1A Human chr17 - 41904788 41904788 41904788 GTTTTTGATTCTCTCTTACTCCAAATCCAGGCAAGATCCTCATCATTGGAGGCAGCATCGCAAAC GTTTTTGATTCTCTCTTACTCCAAATCCAGGCGAGATCCTCATCATTGGAGGCAGCATCGCAAAC T C ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41904685..41904836 26863196 MeRIP-seq:(Medium) rs1237864927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25283192 Human_Splice_Rec_1816970,Human_Splice_Rec_1816971,Human_Splice_Rec_1817026,Human_Splice_Rec_1817027,Human_Splice_Rec_1817082,Human_Splice_Rec_1817083,Human_Splice_Rec_1817176,Human_Splice_Rec_1817177,Human_Splice_Rec_1817224,Human_Splice_Rec_1817225,Human_Splice_Rec_1817232 RMVar_hsa_circ_52809,RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_113752,RMVar_hsa_circ_345873,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_80190,RMVar_hsa_circ_24463,RMVar_hsa_circ_184247,RMVar_hsa_circ_184249,RMVar_hsa_circ_184250,RMVar_hsa_circ_184248,RMVar_hsa_circ_108758,RMVar_hsa_circ_117742,RMVar_hsa_circ_63838,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_184254,RMVar_hsa_circ_184255,RMVar_hsa_circ_337607,RMVar_hsa_circ_281874,RMVar_hsa_circ_330957,RMVar_hsa_circ_281028,RMVar_hsa_circ_184257,RMVar_hsa_circ_184259,RMVar_hsa_circ_184260,RMVar_hsa_circ_184258,RMVar_hsa_circ_287038,RMVar_hsa_circ_48732,RMVar_hsa_circ_367772,RMVar_hsa_circ_357162,RMVar_hsa_circ_184261 108900 RMVar_ID_108900 Human_SNP_ID_624497501 m1A Human chr17 - 41906487 41906487 41906487 AGGGGGTTGCTGAAGGGATGCCAGCCCAGTCTACCCAGCATCAACATGTGTGTAGCCTGGGTGGG AGGGGGTTGCTGAAGGGATGCCAGCCCAGTCTGCCCAGCATCAACATGTGTGTAGCCTGGGTGGG T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41906482..41906602 26863196 MeRIP-seq:(Medium) rs781884100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5366998,Human_RBP_ID_19079069 RMVar_hsa_circ_52809,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_26428,RMVar_hsa_circ_21398,RMVar_hsa_circ_44854,RMVar_hsa_circ_113752,RMVar_hsa_circ_345873,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_24463,RMVar_hsa_circ_184247,RMVar_hsa_circ_184249,RMVar_hsa_circ_184248,RMVar_hsa_circ_108758,RMVar_hsa_circ_117742,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_184254,RMVar_hsa_circ_184255,RMVar_hsa_circ_337607,RMVar_hsa_circ_330957,RMVar_hsa_circ_281028,RMVar_hsa_circ_184259,RMVar_hsa_circ_184260,RMVar_hsa_circ_184258,RMVar_hsa_circ_287038,RMVar_hsa_circ_48732,RMVar_hsa_circ_367772,RMVar_hsa_circ_357162,RMVar_hsa_circ_184261,RMVar_hsa_circ_34737 108901 RMVar_ID_108901 Human_SNP_ID_624498175 m1A Human chr17 - 41909070 41909070 41909070 GGATGAACTGTCCCTCTCTCCCTCCCACCTCTAGAATTCTGGCCAGTTTTATCTCCGGCCTCTTC GGATGAACTGTCCCTCTCTCCCTCCCACCTCTGGAATTCTGGCCAGTTTTATCTCCGGCCTCTTC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41909051..41909075 26863196 MeRIP-seq:(Medium) rs1555633163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8452321 Human_Splice_Rec_1816963,Human_Splice_Rec_1817019,Human_Splice_Rec_1817075,Human_Splice_Rec_1817169,Human_Splice_Rec_1817239 RMVar_hsa_circ_3671,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_113752,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_24463,RMVar_hsa_circ_184247,RMVar_hsa_circ_184248,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_337607,RMVar_hsa_circ_281028,RMVar_hsa_circ_184259,RMVar_hsa_circ_184260,RMVar_hsa_circ_367772,RMVar_hsa_circ_357162,RMVar_hsa_circ_90670,RMVar_hsa_circ_34737,RMVar_hsa_circ_88642,RMVar_hsa_circ_184262,RMVar_hsa_circ_11163,RMVar_hsa_circ_184263,RMVar_hsa_circ_36161 108902 RMVar_ID_108902 Human_SNP_ID_624499389 m1A Human chr17 - 41913902 41913902 41913902 GCCTGCCCCCTTCTGACCAGCTTCTCTCTCCCAGACAGGTAGAGCAGGTCTCTCTGCAGCCATGT GCCTGCCCCCTTCTGACCAGCTTCTCTCTCCCGGACAGGTAGAGCAGGTCTCTCTGCAGCCATGT T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41913876..41913925 26863196 MeRIP-seq:(Medium) rs199697422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_899997,Human_RBP_ID_22657532 RMVar_hsa_circ_99355,RMVar_hsa_circ_184247,RMVar_hsa_circ_90670,RMVar_hsa_circ_184263 108903 RMVar_ID_108903 Human_SNP_ID_624500698 m1A Human chr17 + 41918941 41918941 41918941 TCCACAGGCCCGACGAACCCCGCAAAATCCGGAGCACCCCAGCAGCCGGTAGCTTCCCGGGATCC TCCACAGGCCCGACGAACCCCGCAAAATCCGGGGCACCCCAGCAGCCGGTAGCTTCCCGGGATCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:41918832..41919000;chr17:41918823..41919000;chr17:41918818..41919025;chr17:41918831..41918975 26863196 MeRIP-seq:(Medium) rs1396183853 Functional Loss SNV dbSNP153 33..33 33 - - - 108904 RMVar_ID_108904 Human_SNP_ID_624512770 m1A Human chr17 - 41966847 41966826 41966847 GGAGGGGCGCCACCGTCGCCGCCTCTGCCGGCACCAGCGCTCCGGGGCCGCCCGCCTGCGCGGAG GGAGGGGCGCCACCGTCGCCGCCTCTGCCGGC_____________________GCCTGCGCGGAG CGGGCGGCCCCGGAGCGCTGGT C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr17:41966801..41966900;chr17:41966751..41966925;chr17:41966796..41966918 26863196,26863410,26863196 MeRIP-seq:(Medium) rs1361933355 Functional Loss DEL dbSNP153 33..53 33 - - - 108905 RMVar_ID_108905 Human_SNP_ID_624514769 m1A Human chr17 + 41973746 41973746 41973746 GCGGCAGGAGAAGGGGGGCAGCCGAGGCGAGGAGGTGGGCGAGCTAAGCCGGGGCAAGCTCTATT GCGGCAGGAGAAGGGGGGCAGCCGAGGCGAGGGGGTGGGCGAGCTAAGCCGGGGCAAGCTCTATT A G CNP Ensembl:ENSG00000173786 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41973562..41973883 26863196 MeRIP-seq:(Medium) rs782166517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767425,Human_RBP_ID_5144184,Human_RBP_ID_5526312,Human_RBP_ID_6594521,Human_RBP_ID_8825525,Human_RBP_ID_17654693,Human_RBP_ID_22443656,Human_RBP_ID_24479070,Human_RBP_ID_27254102 108906 RMVar_ID_108906 Human_SNP_ID_624514998 m1A Human chr17 - 41974262 41974257 41974262 TGTCTCCCCACTCACCCAGCTCTGGGCAGAGCAGCTGGGCTGGGCTGGGGCTGAGCTAACCAGAA TGTCTCCCCACTCACCCAGCTCTGGGCAGAGC_____GGCTGGGCTGGGGCTGAGCTAACCAGAA CCAGCT C lnc-DNAJC7-1 RNACentral:URS0000D58C87 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41974092..41974293 32194978 MeRIP-seq:(Medium) rs1295230413 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_6594542,Human_RBP_ID_13004529 108907 RMVar_ID_108907 Human_SNP_ID_624515000 m1A Human chr17 - 41974262 41974262 41974262 TGTCTCCCCACTCACCCAGCTCTGGGCAGAGCAGCTGGGCTGGGCTGGGGCTGAGCTAACCAGAA TGTCTCCCCACTCACCCAGCTCTGGGCAGAGCTGCTGGGCTGGGCTGGGGCTGAGCTAACCAGAA T A lnc-DNAJC7-1 RNACentral:URS0000D58C87 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:41974092..41974293 32194978 MeRIP-seq:(Medium) rs781921912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6594542,Human_RBP_ID_13004529 108908 RMVar_ID_108908 Human_SNP_ID_624515198 m1A Human chr17 - 41975037 41975037 41975037 GATTAGCAAGGCCCTGTTACTGAACAGAGGGCAGTGGAGGGCACCCCAGGAACCACAGCACACAG GATTAGCAAGGCCCTGTTACTGAACAGAGGGCCGTGGAGGGCACCCCAGGAACCACAGCACACAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:41974989..41975190 32194978 MeRIP-seq:(Medium) rs1186920097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13004560 108909 RMVar_ID_108909 Human_SNP_ID_624516035 m1A Human chr17 - 41978368 41978368 41978368 GGAGTTGGTTGCTATTCAGATGTGTTGGGGAAAGTGACAGGCATAGCTGACTCGGGGTCATTCAC GGAGTTGGTTGCTATTCAGATGTGTTGGGGAAGGTGACAGGCATAGCTGACTCGGGGTCATTCAC T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:41978366..41978461 26863196 MeRIP-seq:(Medium) rs1270136476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6594607,Human_RBP_ID_13004691,Human_RBP_ID_17566472 RMVar_hsa_circ_184269,RMVar_hsa_circ_64204,RMVar_hsa_circ_375883,RMVar_hsa_circ_30694 108910 RMVar_ID_108910 Human_SNP_ID_624516962 m1A Human chr17 + 41981988 41981988 41981988 AACTTCTTCTCCTCCTCCTTCTGAACCTCAGCACTGGCTCCACTATGCCGATCTAAAGTGGGGAG AACTTCTTCTCCTCCTCCTTCTGAACCTCAGCGCTGGCTCCACTATGCCGATCTAAAGTGGGGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:41981851..41982039;chr17:41981876..41982046 26863196 MeRIP-seq:(Medium) rs1272743081 Functional Loss SNV dbSNP153 33..33 33 - - - 108911 RMVar_ID_108911 Human_SNP_ID_624522172 m1A Human chr17 - 42003509 42003509 42003509 TCTCATCCTTCAGTCCCTTTGCTGTAAAGGCAACTTGAACAAGCTTCAGCCCTTTCTCAGACTTC TCTCATCCTTCAGTCCCTTTGCTGTAAAGGCAGCTTGAACAAGCTTCAGCCCTTTCTCAGACTTC T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42003507..42003593 26863196 MeRIP-seq:(Medium) rs1355953753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1817494,Human_Splice_Rec_1817610,Human_Splice_Rec_1817690,Human_Splice_Rec_1817872,Human_Splice_Rec_1818138,Human_Splice_Rec_1818154 RMVar_hsa_circ_276235,RMVar_hsa_circ_184276,RMVar_hsa_circ_278318,RMVar_hsa_circ_322239,RMVar_hsa_circ_184278,RMVar_hsa_circ_270520 108912 RMVar_ID_108912 Human_SNP_ID_624525539 m1A Human chr17 - 42017394 42017394 42017394 CGGCGGTAAGATGGCGGCTGCCGCGGAGTGCGATGTGGTAATGGCGGCGACCGAGCCGGAGCTGC CGGCGGTAAGATGGCGGCTGCCGCGGAGTGCGTTGTGGTAATGGCGGCGACCGAGCCGGAGCTGC T A DNAJC7 Ensembl:ENSG00000168259 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42017250..42017450 26863196 MeRIP-seq:(Medium) rs200438343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489454,Human_RBP_ID_767306,Human_RBP_ID_4465387,Human_RBP_ID_5467383,Human_RBP_ID_23726263,Human_RBP_ID_26333336,Human_RBP_ID_26961197,Human_RBP_ID_27812684,Human_RBP_ID_27838443 Human_Splice_Rec_1817341,Human_Splice_Rec_1817365,Human_Splice_Rec_1817395,Human_Splice_Rec_1817423,Human_Splice_Rec_1817493,Human_Splice_Rec_1817529,Human_Splice_Rec_1817583,Human_Splice_Rec_1817639,Human_Splice_Rec_1817689,Human_Splice_Rec_1817767,Human_Splice_Rec_1817845,Human_Splice_Rec_1817949,Human_Splice_Rec_1817975,Human_Splice_Rec_1817997,Human_Splice_Rec_1818043,Human_Splice_Rec_1818079,Human_Splice_Rec_1818147 108913 RMVar_ID_108913 Human_SNP_ID_624525540 m1A Human chr17 - 42017394 42017394 42017394 CGGCGGTAAGATGGCGGCTGCCGCGGAGTGCGATGTGGTAATGGCGGCGACCGAGCCGGAGCTGC CGGCGGTAAGATGGCGGCTGCCGCGGAGTGCGGTGTGGTAATGGCGGCGACCGAGCCGGAGCTGC T C DNAJC7 Ensembl:ENSG00000168259 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42017250..42017450 26863196 MeRIP-seq:(Medium) rs200438343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489454,Human_RBP_ID_767306,Human_RBP_ID_4465387,Human_RBP_ID_5467383,Human_RBP_ID_23726263,Human_RBP_ID_26333336,Human_RBP_ID_26961197,Human_RBP_ID_27812684,Human_RBP_ID_27838443 Human_Splice_Rec_1817341,Human_Splice_Rec_1817365,Human_Splice_Rec_1817395,Human_Splice_Rec_1817423,Human_Splice_Rec_1817493,Human_Splice_Rec_1817529,Human_Splice_Rec_1817583,Human_Splice_Rec_1817639,Human_Splice_Rec_1817689,Human_Splice_Rec_1817767,Human_Splice_Rec_1817845,Human_Splice_Rec_1817949,Human_Splice_Rec_1817975,Human_Splice_Rec_1817997,Human_Splice_Rec_1818043,Human_Splice_Rec_1818079,Human_Splice_Rec_1818147 108914 RMVar_ID_108914 Human_SNP_ID_624525547 m1A Human chr17 - 42017400 42017400 42017400 TGGTCCCGGCGGTAAGATGGCGGCTGCCGCGGAGTGCGATGTGGTAATGGCGGCGACCGAGCCGG TGGTCCCGGCGGTAAGATGGCGGCTGCCGCGGCGTGCGATGTGGTAATGGCGGCGACCGAGCCGG T G DNAJC7 Ensembl:ENSG00000168259 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42017276..42017475 26863196 MeRIP-seq:(Medium) rs1254522773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489454,Human_RBP_ID_767306,Human_RBP_ID_4465387,Human_RBP_ID_5467383,Human_RBP_ID_23726263,Human_RBP_ID_26333336,Human_RBP_ID_26961197,Human_RBP_ID_27812684,Human_RBP_ID_27838443 Human_Splice_Rec_1817341,Human_Splice_Rec_1817365,Human_Splice_Rec_1817395,Human_Splice_Rec_1817423,Human_Splice_Rec_1817493,Human_Splice_Rec_1817529,Human_Splice_Rec_1817583,Human_Splice_Rec_1817639,Human_Splice_Rec_1817689,Human_Splice_Rec_1817767,Human_Splice_Rec_1817845,Human_Splice_Rec_1817949,Human_Splice_Rec_1817975,Human_Splice_Rec_1817997,Human_Splice_Rec_1818043,Human_Splice_Rec_1818079,Human_Splice_Rec_1818147 108915 RMVar_ID_108915 Human_SNP_ID_624526351 m1A Human chr17 - 42020149 42020149 42020149 GCCGGGCCCTCCGAGCTCGCGGGGACCAGGGGAGGGGCAGCGCCGCCGCAAAGGCTCCAGTCTTC GCCGGGCCCTCCGAGCTCGCGGGGACCAGGGGCGGGGCAGCGCCGCCGCAAAGGCTCCAGTCTTC T G DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:42020101..42020255;chr17:42020076..42020422;chr17:42020076..42020259 26863196 MeRIP-seq:(Medium) rs1049354623 Functional Loss SNV dbSNP153 33..33 33 - - - 108916 RMVar_ID_108916 Human_SNP_ID_624526976 m1A Human chr17 - 42022362 42022362 42022362 TATAAAATGAGAAAACTGTCTGAAGTGGAGAGAGAGATGGGAAATGTGAGTGATGAGAGCATCTT TATAAAATGAGAAAACTGTCTGAAGTGGAGAGCGAGATGGGAAATGTGAGTGATGAGAGCATCTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42022360..42022584 26863196 MeRIP-seq:(Medium) rs1308641748 Functional Loss SNV dbSNP153 33..33 33 - - - 108917 RMVar_ID_108917 Human_SNP_ID_624526981 m1A Human chr17 + 42022378 42022378 42022378 TCACATTTCCCATCTCTCTCTCCACTTCAGACAGTTTTCTCATTTTATACCAGGTTCGGAGATGA TCACATTTCCCATCTCTCTCTCCACTTCAGACGGTTTTCTCATTTTATACCAGGTTCGGAGATGA A G NKIRAS2 Ensembl:ENSG00000168256 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:42022376..42022475;chr17:42022376..42022450 26863196 MeRIP-seq:(Medium) rs1555653229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1818183,Human_Splice_Rec_1818191,Human_Splice_Rec_1818222,Human_Splice_Rec_1818229 RMVar_hsa_circ_85465,RMVar_hsa_circ_111683,RMVar_hsa_circ_184280,RMVar_hsa_circ_71126,RMVar_hsa_circ_77651,RMVar_hsa_circ_184281,RMVar_hsa_circ_184282 108918 RMVar_ID_108918 Human_SNP_ID_624527738 m1A Human chr17 + 42025105 42025105 42025105 CGCTCCCTCCAGCCACCAGGGGGCAGGAGTGCACTACCTGCTGTCAGTCACCAGAGTGGCCGCTC CGCTCCCTCCAGCCACCAGGGGGCAGGAGTGCGCTACCTGCTGTCAGTCACCAGAGTGGCCGCTC A G NKIRAS2 Ensembl:ENSG00000168256 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:42024997..42025147 32194978 MeRIP-seq:(Medium) rs537066781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8191078,Human_RBP_ID_26450755 Human_miRNA_ID_212396,Human_miRNA_ID_221928,Human_miRNA_ID_291879,Human_miRNA_ID_491425,Human_miRNA_ID_494683,Human_miRNA_ID_760455,Human_miRNA_ID_765373,Human_miRNA_ID_1324947,Human_miRNA_ID_2037847,Human_miRNA_ID_2037848,Human_miRNA_ID_2168769,Human_miRNA_ID_2168770,Human_miRNA_ID_2170292,Human_miRNA_ID_2170293,Human_miRNA_ID_2223376,Human_miRNA_ID_2223377,Human_miRNA_ID_2348547,Human_miRNA_ID_2348548,Human_miRNA_ID_2486447,Human_miRNA_ID_2486448,Human_miRNA_ID_3074812,Human_miRNA_ID_3074813 RMVar_hsa_circ_85465,RMVar_hsa_circ_77651,RMVar_hsa_circ_184281,RMVar_hsa_circ_184282 108919 RMVar_ID_108919 Human_SNP_ID_624533575 m1A Human chr17 + 42048061 42048061 42048061 TCCCATGTTCCTTGGTTTTCCTTCCTCTGTCCATCACTCCTTGGCCTCTGGAGGTCATCTCCTCC TCCCATGTTCCTTGGTTTTCCTTCCTCTGTCCCTCACTCCTTGGCCTCTGGAGGTCATCTCCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42048052..42048149 26863196 MeRIP-seq:(Medium) rs1468829346 Functional Loss SNV dbSNP153 33..33 33 - - - 108920 RMVar_ID_108920 Human_SNP_ID_624533576 m1A Human chr17 + 42048061 42048061 42048061 TCCCATGTTCCTTGGTTTTCCTTCCTCTGTCCATCACTCCTTGGCCTCTGGAGGTCATCTCCTCC TCCCATGTTCCTTGGTTTTCCTTCCTCTGTCCGTCACTCCTTGGCCTCTGGAGGTCATCTCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42048052..42048149 26863196 MeRIP-seq:(Medium) rs1468829346 Functional Loss SNV dbSNP153 33..33 33 - - - 108921 RMVar_ID_108921 Human_SNP_ID_624533823 m1A Human chr17 - 42049086 42049086 42049086 TGGAGGAACCCAGAGAGAAGGGTGGTGTTACTAGGAAGGAAGGGAGACACAAGTGGCCACCAGAG TGGAGGAACCCAGAGAGAAGGGTGGTGTTACTGGGAAGGAAGGGAGACACAAGTGGCCACCAGAG T C ZNF385C,C17orf113 Ensembl:ENSG00000187595,Ensembl:ENSG00000267221 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42049074..42049235 26863196 MeRIP-seq:(Medium) rs1386631506 Functional Loss SNV dbSNP153 33..33 33 - - - 108922 RMVar_ID_108922 Human_SNP_ID_624533842 m1A Human chr17 + 42049194 42049194 42049194 CCTTCTTCCAGAATATTCCCAGCTGCCCTCCCAATGCTTTACCTGGCCTGTTTCATTTCCCCTTT CCTTCTTCCAGAATATTCCCAGCTGCCCTCCCGATGCTTTACCTGGCCTGTTTCATTTCCCCTTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42049014..42049281 26863196 MeRIP-seq:(Medium) rs782604119 Functional Loss SNV dbSNP153 33..33 33 - - - 108923 RMVar_ID_108923 Human_SNP_ID_624549723 m1A Human chr17 + 42113839 42113839 42113839 AGCGGCTTCGCAGCCGCTCAGTCATGGTCTTCAGGTCTGGGGCAGCAGGAGACGGAGCACAGCTT AGCGGCTTCGCAGCCGCTCAGTCATGGTCTTCCGGTCTGGGGCAGCAGGAGACGGAGCACAGCTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42113709..42113863 26863196 MeRIP-seq:(Medium) rs782557255 Functional Loss SNV dbSNP153 33..33 33 - - - 108924 RMVar_ID_108924 Human_SNP_ID_624551522 m1A Human chr17 - 42119528 42119528 42119528 TACCTACAAGGTCAATTACACCAGGTAGGCCCAGCCAGGGGCAGCTTCGGGGGAGGCTTGCAGGC TACCTACAAGGTCAATTACACCAGGTAGGCCCCGCCAGGGGCAGCTTCGGGGGAGGCTTGCAGGC T G KAT2A Ensembl:ENSG00000108773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42119526..42119575 26863196 MeRIP-seq:(Medium) rs781982924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19079092,Human_RBP_ID_23256898,Human_RBP_ID_26782272 RMVar_hsa_circ_184288,RMVar_hsa_circ_104099,RMVar_hsa_circ_111845,RMVar_hsa_circ_90640,RMVar_hsa_circ_81488,RMVar_hsa_circ_184290,RMVar_hsa_circ_184289,RMVar_hsa_circ_184287,RMVar_hsa_circ_119273,RMVar_hsa_circ_93964,RMVar_hsa_circ_184301,RMVar_hsa_circ_97657,RMVar_hsa_circ_184303,RMVar_hsa_circ_184304 108925 RMVar_ID_108925 Human_SNP_ID_624552150 m1A Human chr17 + 42121224 42121224 42121224 GGGGCTGAAGCCGGGCTGGGTGCAGGAGTCGGAGTTGGGGCAGGGGCTGGGGACTGAAGGGGCCG GGGGCTGAAGCCGGGCTGGGTGCAGGAGTCGGGGTTGGGGCAGGGGCTGGGGACTGAAGGGGCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:42120951..42121350;chr17:42121134..42121350 26863196 MeRIP-seq:(Medium) rs1199396049 Functional Loss SNV dbSNP153 33..33 33 - - - 108926 RMVar_ID_108926 Human_SNP_ID_624552173 m1A Human chr17 + 42121266 42121266 42121266 GGGGCTGGGGACTGAAGGGGCCGGGGCTGCGCAGCCGGGGCCGGGGTCGGGGCCTGGGAAGGTTC GGGGCTGGGGACTGAAGGGGCCGGGGCTGCGCCGCCGGGGCCGGGGTCGGGGCCTGGGAAGGTTC A C - - Other Unknown GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr17:42121208..42121308 26863410 MeRIP-seq:(Medium) rs541424646 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 108927 RMVar_ID_108927 Human_SNP_ID_624552191 m1A Human chr17 - 42121296 42121296 42121296 CCGCTCTCCGCTGCGGGGGAGGCCATGGCGGAACCTTCCCAGGCCCCGACCCCGGCCCCGGCTGC CCGCTCTCCGCTGCGGGGGAGGCCATGGCGGAGCCTTCCCAGGCCCCGACCCCGGCCCCGGCTGC T C AC099811.2,KAT2A Ensembl:ENSG00000267261,Ensembl:ENSG00000108773 Protein coding,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42121157..42121325 26863196 MeRIP-seq:(Medium) rs1555667373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419601,Human_RBP_ID_18697744 RMVar_hsa_circ_111845,RMVar_hsa_circ_25379,RMVar_hsa_circ_184287 108928 RMVar_ID_108928 Human_SNP_ID_624552192 m1A Human chr17 - 42121297 42121297 42121297 GCCGCTCTCCGCTGCGGGGGAGGCCATGGCGGAACCTTCCCAGGCCCCGACCCCGGCCCCGGCTG GCCGCTCTCCGCTGCGGGGGAGGCCATGGCGGCACCTTCCCAGGCCCCGACCCCGGCCCCGGCTG T G AC099811.2,KAT2A Ensembl:ENSG00000267261,Ensembl:ENSG00000108773 Protein coding,Protein coding intron,CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:42121219..42121301 26863410 MeRIP-seq:(Medium) rs374471583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419601,Human_RBP_ID_18697744 RMVar_hsa_circ_111845,RMVar_hsa_circ_25379,RMVar_hsa_circ_184287 108929 RMVar_ID_108929 Human_SNP_ID_624552198 m1A Human chr17 - 42121304 42121304 42121304 GCGCGGCGCCGCTCTCCGCTGCGGGGGAGGCCATGGCGGAACCTTCCCAGGCCCCGACCCCGGCC GCGCGGCGCCGCTCTCCGCTGCGGGGGAGGCCGTGGCGGAACCTTCCCAGGCCCCGACCCCGGCC T C AC099811.2,KAT2A Ensembl:ENSG00000267261,Ensembl:ENSG00000108773 Protein coding,Protein coding intron,start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:42121220..42121304 26863410 MeRIP-seq:(Medium) rs1428349409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419601,Human_RBP_ID_18438994,Human_RBP_ID_18697744 RMVar_hsa_circ_111845,RMVar_hsa_circ_25379,RMVar_hsa_circ_184287 108930 RMVar_ID_108930 Human_SNP_ID_624553537 m1A Human chr17 - 42125200 42125200 42125200 CACAGCATTATCACAGCATTATTGTGACAGCCACGAACCCATTGCCCACAACCCCTCCACCCTCG CACAGCATTATCACAGCATTATTGTGACAGCCGCGAACCCATTGCCCACAACCCCTCCACCCTCG T C AC099811.2,RAB5C Ensembl:ENSG00000267261,Ensembl:ENSG00000108774 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42125152..42125252 26863196 MeRIP-seq:(Medium) rs1555668448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1533905,Human_RBP_ID_1858194,Human_RBP_ID_4473072,Human_RBP_ID_8191080,Human_RBP_ID_8452485,Human_RBP_ID_13006064,Human_RBP_ID_17259803,Human_RBP_ID_17378362,Human_RBP_ID_17491291,Human_RBP_ID_17654698,Human_RBP_ID_17892373,Human_RBP_ID_18943183 RMVar_hsa_circ_25379,RMVar_hsa_circ_184309,RMVar_hsa_circ_109117 108931 RMVar_ID_108931 Human_SNP_ID_624553749 m1A Human chr17 - 42125826 42125826 42125826 TGCTCCAGGCCGAAACCGAGGTGTGGACCTCCAGGAGAACAACCCAGCCAGCCGGAGCCAGTGCT TGCTCCAGGCCGAAACCGAGGTGTGGACCTCCGGGAGAACAACCCAGCCAGCCGGAGCCAGTGCT T C AC099811.2,RAB5C Ensembl:ENSG00000267261,Ensembl:ENSG00000108774 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42125344..42125900 26863196 MeRIP-seq:(Medium) rs1555668647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238713,Human_RBP_ID_1533912,Human_RBP_ID_8452498,Human_RBP_ID_13006085,Human_RBP_ID_26812330 Human_Splice_Rec_1818504,Human_Splice_Rec_1818514,Human_Splice_Rec_1818526 Human_miRNA_ID_2332921,Human_miRNA_ID_2966005 RMVar_hsa_circ_25379,RMVar_hsa_circ_184309,RMVar_hsa_circ_109117 108932 RMVar_ID_108932 Human_SNP_ID_624554954 m1A Human chr17 + 42130413 42130413 42130413 AAGCGGAGGACGAGGCTGGATTTGCCTACCGCAGACTCCCCCAGCAGAACCAGCTTAAATTGACA AAGCGGAGGACGAGGCTGGATTTGCCTACCGCCGACTCCCCCAGCAGAACCAGCTTAAATTGACA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42130363..42131625 32194978 MeRIP-seq:(Medium) rs746412388 Functional Loss SNV dbSNP153 33..33 33 - - - 108933 RMVar_ID_108933 Human_SNP_ID_624554955 m1A Human chr17 + 42130413 42130413 42130413 AAGCGGAGGACGAGGCTGGATTTGCCTACCGCAGACTCCCCCAGCAGAACCAGCTTAAATTGACA AAGCGGAGGACGAGGCTGGATTTGCCTACCGCGGACTCCCCCAGCAGAACCAGCTTAAATTGACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42130363..42131625 32194978 MeRIP-seq:(Medium) rs746412388 Functional Loss SNV dbSNP153 33..33 33 - - - 108934 RMVar_ID_108934 Human_SNP_ID_624555024 m1A Human chr17 + 42130583 42130583 42130583 GCTATGCAAAGAGGCACTTAGTGGGGAGGGGGACCTCCAACTGTAAGGGAGAAATGAGAAGTACT GCTATGCAAAGAGGCACTTAGTGGGGAGGGGGGCCTCCAACTGTAAGGGAGAAATGAGAAGTACT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:42130513..42154926 26863410 MeRIP-seq:(Medium) rs752383662 Functional Loss SNV dbSNP153 33..33 33 - - - 108935 RMVar_ID_108935 Human_SNP_ID_624561243 m1A Human chr17 - 42154941 42154941 42154941 GCCTGGGACACCGCCGGCGGGGAGAGAAGCGGATCCCGTCCGAGCCCCGGCCCCAAGTAACGCCG GCCTGGGACACCGCCGGCGGGGAGAGAAGCGGGTCCCGTCCGAGCCCCGGCCCCAAGTAACGCCG T C RAB5C Ensembl:ENSG00000108774 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:42154832..42155000;chr17:42154823..42155000 26863196 MeRIP-seq:(Medium) rs890099004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768270,Human_RBP_ID_4464547,Human_RBP_ID_5441452,Human_RBP_ID_22445496,Human_RBP_ID_22959815,Human_RBP_ID_23726394 Human_Splice_Rec_1818479,Human_Splice_Rec_1818493,Human_Splice_Rec_1818505,Human_Splice_Rec_1818515,Human_Splice_Rec_1818537,Human_Splice_Rec_1818545,Human_Splice_Rec_1818551 RMVar_hsa_circ_184313 108936 RMVar_ID_108936 Human_SNP_ID_624561244 m1A Human chr17 - 42154941 42154941 42154941 GCCTGGGACACCGCCGGCGGGGAGAGAAGCGGATCCCGTCCGAGCCCCGGCCCCAAGTAACGCCG GCCTGGGACACCGCCGGCGGGGAGAGAAGCGGCTCCCGTCCGAGCCCCGGCCCCAAGTAACGCCG T G RAB5C Ensembl:ENSG00000108774 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:42154832..42155000;chr17:42154823..42155000 26863196 MeRIP-seq:(Medium) rs890099004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768270,Human_RBP_ID_4464547,Human_RBP_ID_5441452,Human_RBP_ID_22445496,Human_RBP_ID_22959815,Human_RBP_ID_23726394 Human_Splice_Rec_1818479,Human_Splice_Rec_1818493,Human_Splice_Rec_1818505,Human_Splice_Rec_1818515,Human_Splice_Rec_1818537,Human_Splice_Rec_1818545,Human_Splice_Rec_1818551 RMVar_hsa_circ_184313 108937 RMVar_ID_108937 Human_SNP_ID_624564810 m1A Human chr17 + 42168050 42168050 42168050 TTTTGTGCCATCACTTCTGGCCTGTGTCCCTAAGGCCATTTCTACCTGGCATTGCCACCTTCCTT TTTTGTGCCATCACTTCTGGCCTGTGTCCCTAGGGCCATTTCTACCTGGCATTGCCACCTTCCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42167928..42168123 26863196 MeRIP-seq:(Medium) rs1364615381 Functional Loss SNV dbSNP153 33..33 33 - - - 108938 RMVar_ID_108938 Human_SNP_ID_624581582 m1A Human chr17 - 42232102 42232102 42232102 GTAAACCATGGCTGTGTGGATACAAGCTCAGCAGCTCCAAGGAGAAGCCCTTCATCAGATGCAAG GTAAACCATGGCTGTGTGGATACAAGCTCAGCTGCTCCAAGGAGAAGCCCTTCATCAGATGCAAG T A STAT5B Ensembl:ENSG00000173757 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42232051..42232202 26863196 MeRIP-seq:(Medium) rs1157720602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49126,Human_RBP_ID_1858217,Human_RBP_ID_3952394,Human_RBP_ID_18697794,Human_RBP_ID_25283824,Human_RBP_ID_26333354 Human_Splice_Rec_1818748,Human_Splice_Rec_1818806,Human_Splice_Rec_1818822 Human_miRNA_ID_2616050 RMVar_hsa_circ_19338,RMVar_hsa_circ_53270,RMVar_hsa_circ_38628,RMVar_hsa_circ_363128,RMVar_hsa_circ_285777,RMVar_hsa_circ_286225,RMVar_hsa_circ_184325,RMVar_hsa_circ_184320,RMVar_hsa_circ_287856,RMVar_hsa_circ_184324,RMVar_hsa_circ_289244,RMVar_hsa_circ_273201,RMVar_hsa_circ_184327,RMVar_hsa_circ_307983,RMVar_hsa_circ_184326 108939 RMVar_ID_108939 Human_SNP_ID_624592150 m1A Human chr17 - 42275418 42275418 42275418 AAACACTTGTAGCCAGCAGTGATGGAAAAGCCAAAGAAGAAAACCAAGTGTCAGCTTTTAGAAAG AAACACTTGTAGCCAGCAGTGATGGAAAAGCCGAAGAAGAAAACCAAGTGTCAGCTTTTAGAAAG T C AC099811.5,STAT5B Ensembl:ENSG00000278829,Ensembl:ENSG00000173757 lincRNA,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42275415..42275638 26863196 MeRIP-seq:(Medium) rs961642026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1090561,Human_RBP_ID_26331816 108940 RMVar_ID_108940 Human_SNP_ID_624602987 m1A Human chr17 - 42317392 42317392 42317392 CACAGCTGCTAGTGCCTGGGAGATCAAATAGTATAAATGAGGGCAGACAACCCTGAGGGGCAGAT CACAGCTGCTAGTGCCTGGGAGATCAAATAGTGTAAATGAGGGCAGACAACCCTGAGGGGCAGAT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42317390..42317509 26863196 MeRIP-seq:(Medium) rs1025078714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465400,Human_RBP_ID_22588103 RMVar_hsa_circ_12314,RMVar_hsa_circ_116857,RMVar_hsa_circ_125461,RMVar_hsa_circ_93665,RMVar_hsa_circ_104685,RMVar_hsa_circ_184339,RMVar_hsa_circ_184341,RMVar_hsa_circ_184342,RMVar_hsa_circ_184340,RMVar_hsa_circ_105319,RMVar_hsa_circ_184345,RMVar_hsa_circ_94403,RMVar_hsa_circ_127938,RMVar_hsa_circ_184344,RMVar_hsa_circ_100328,RMVar_hsa_circ_4537,RMVar_hsa_circ_76369,RMVar_hsa_circ_184347,RMVar_hsa_circ_184348,RMVar_hsa_circ_184346 108941 RMVar_ID_108941 Human_SNP_ID_624619829 m1A Human chr17 + 42388192 42388191 42388192 TCTCCCGGCCCCACTGCAGCGTCCATCACAACATCCCCAAGGTCCCAGAGGCCCCCTGCCGCTGC TCTCCCGGCCCCACTGCAGCGTCCATCACAAC_TCCCCAAGGTCCCAGAGGCCCCCTGCCGCTGC CA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42388189..42388475 26863196 MeRIP-seq:(Medium) rs1273865825 Functional Loss DEL dbSNP153 33..33 33 - - - 108942 RMVar_ID_108942 Human_SNP_ID_624623764 m1A Human chr17 + 42402843 42402842 42402843 TCGGGGCCTCCCTTCAGGCTGTGACTGGGGAGAGGGGCTGTTCTTGCTTCTGACAAACCCCCTTT TCGGGGCCTCCCTTCAGGCTGTGACTGGGGAG_GGGGCTGTTCTTGCTTCTGACAAACCCCCTTT GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:42402476..42402950 32194978 MeRIP-seq:(Medium) rs1165199756 Functional Loss DEL dbSNP153 33..33 33 - - - 108943 RMVar_ID_108943 Human_SNP_ID_624623769 m1A Human chr17 + 42402876 42402876 42402876 GGGGCTGTTCTTGCTTCTGACAAACCCCCTTTAATGGGGAGGAACAAGGGGACTCGTGTCTTGAG GGGGCTGTTCTTGCTTCTGACAAACCCCCTTTTATGGGGAGGAACAAGGGGACTCGTGTCTTGAG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42402825..42402914 26863196 MeRIP-seq:(Medium) rs1196934871 Functional Loss SNV dbSNP153 33..33 33 - - - 108944 RMVar_ID_108944 Human_SNP_ID_624624191 m1A Human chr17 + 42404624 42404624 42404624 ATTTAGAAAAATCTCAGCCAGCTCGAGCCGAGAGAGAATGCGAAAGAGGAAGTTCGGAAGGAGCG ATTTAGAAAAATCTCAGCCAGCTCGAGCCGAGGGAGAATGCGAAAGAGGAAGTTCGGAAGGAGCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:42404580..42405000 26863196 MeRIP-seq:(Medium) rs908060704 Functional Loss SNV dbSNP153 33..33 33 - - - 108945 RMVar_ID_108945 Human_SNP_ID_624624464 m1A Human chr17 + 42405222 42405222 42405222 TGCGCTTGATACGCTCTGCGCGGGACTCCTCAATAACCTCCTCAACCTCCACCGCCTCGTCCGAC TGCGCTTGATACGCTCTGCGCGGGACTCCTCAGTAACCTCCTCAACCTCCACCGCCTCGTCCGAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42404526..42405400 26863196 MeRIP-seq:(Medium) rs146929422 Functional Loss SNV dbSNP153 33..33 33 - - - 108946 RMVar_ID_108946 Human_SNP_ID_624624510 m1A Human chr17 - 42405323 42405323 42405323 AGCAAATCGCTGAAAGAGTCGGAGGCGCTGCCAGAGAAGGAGGGCGAGGAGCTGGGCGAGGGCGA AGCAAATCGCTGAAAGAGTCGGAGGCGCTGCCGGAGAAGGAGGGCGAGGAGCTGGGCGAGGGCGA T C CAVIN1 Ensembl:ENSG00000177469 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42405026..42405350 26863196 MeRIP-seq:(Medium) rs968331945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49307,Human_RBP_ID_4427709,Human_RBP_ID_9289119 Human_Splice_Rec_1819284 Human_miRNA_ID_3118718 RMVar_hsa_circ_112675,RMVar_hsa_circ_126991,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_184365,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 108947 RMVar_ID_108947 Human_SNP_ID_624624511 m1A Human chr17 - 42405323 42405323 42405323 AGCAAATCGCTGAAAGAGTCGGAGGCGCTGCCAGAGAAGGAGGGCGAGGAGCTGGGCGAGGGCGA AGCAAATCGCTGAAAGAGTCGGAGGCGCTGCCCGAGAAGGAGGGCGAGGAGCTGGGCGAGGGCGA T G CAVIN1 Ensembl:ENSG00000177469 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42405026..42405350 26863196 MeRIP-seq:(Medium) rs968331945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49307,Human_RBP_ID_4427709,Human_RBP_ID_9289119 Human_Splice_Rec_1819284 Human_miRNA_ID_3118718 RMVar_hsa_circ_112675,RMVar_hsa_circ_126991,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_184365,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 108948 RMVar_ID_108948 Human_SNP_ID_624628940 m1A Human chr17 - 42422677 42422677 42422677 GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCAACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCTACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT T A CAVIN1 Ensembl:ENSG00000177469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42422600..42422994 26863196 MeRIP-seq:(Medium) rs201698896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49311,Human_RBP_ID_4427712,Human_RBP_ID_22444600,Human_RBP_ID_26812380 Human_Splice_Rec_1819283 RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 108949 RMVar_ID_108949 Human_SNP_ID_624628941 m1A Human chr17 - 42422677 42422677 42422677 GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCAACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCGACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT T C CAVIN1 Ensembl:ENSG00000177469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42422600..42422994 26863196 MeRIP-seq:(Medium) rs201698896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49311,Human_RBP_ID_4427712,Human_RBP_ID_22444600,Human_RBP_ID_26812380 Human_Splice_Rec_1819283 RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 108950 RMVar_ID_108950 Human_SNP_ID_624628942 m1A Human chr17 - 42422677 42422677 42422677 GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCAACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT GCCAGGCGGGGCAGATCAAGAAGCTGGAGGTCCACGAGGCCGAGCTGCTGCGGCGCCGCAACTTT T G CAVIN1 Ensembl:ENSG00000177469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42422600..42422994 26863196 MeRIP-seq:(Medium) rs201698896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49311,Human_RBP_ID_4427712,Human_RBP_ID_22444600,Human_RBP_ID_26812380 Human_Splice_Rec_1819283 RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 108951 RMVar_ID_108951 Human_SNP_ID_624629033 m1A Human chr17 + 42422853 42422853 42422853 GCTCGCCCTGGATGCTCTGCACTGCGCCCTCCATCTCCGCCTGCCGCTCCTCCAGCTGTGCTTGA GCTCGCCCTGGATGCTCTGCACTGCGCCCTCCGTCTCCGCCTGCCGCTCCTCCAGCTGTGCTTGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42422605..42422994 26863196 MeRIP-seq:(Medium) rs1244823716 Functional Loss SNV dbSNP153 33..33 33 - - - 108952 RMVar_ID_108952 Human_SNP_ID_624638761 m1A Human chr17 + 42458962 42458962 42458962 GTTTCTGTGGCGGTTGCTGTGGCGGAGTTTGGAGGTGAGTGGGGGCTGTAGGTTTAGCGCAACAG GTTTCTGTGGCGGTTGCTGTGGCGGAGTTTGGGGGTGAGTGGGGGCTGTAGGTTTAGCGCAACAG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42458925..42459032 26863196 MeRIP-seq:(Medium) rs1342384734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952414,Human_RBP_ID_5362796,Human_RBP_ID_18419604,Human_RBP_ID_18991328,Human_RBP_ID_19079122,Human_RBP_ID_26769521 Human_Splice_Rec_1819285,Human_Splice_Rec_1819325,Human_Splice_Rec_1819333,Human_Splice_Rec_1819343,Human_Splice_Rec_1819381,Human_Splice_Rec_1819421,Human_Splice_Rec_1819461,Human_Splice_Rec_1819503,Human_Splice_Rec_1819531 108953 RMVar_ID_108953 Human_SNP_ID_624657795 m1A Human chr17 - 42536301 42536295 42536301 CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCACCGCCGCGGCCACCGCCACCGCCTCCATGGTC CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCC______GCGGCCACCGCCACCGCCTCCATGGTC CGGCGGT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42536251..42538341;chr17:42536251..42536946 26863196 MeRIP-seq:(Medium) rs1555621405 Functional Loss DEL dbSNP153 33..38 33 - - - Clinvar_Rec_703 108954 RMVar_ID_108954 Human_SNP_ID_624657799 m1A Human chr17 - 42536301 42536301 42536301 CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCACCGCCGCGGCCACCGCCACCGCCTCCATGGTC CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCCCCGCCGCGGCCACCGCCACCGCCTCCATGGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42536251..42538341;chr17:42536251..42536946 26863196 MeRIP-seq:(Medium) rs794726879 Functional Loss SNV dbSNP153 33..33 33 - - - 108955 RMVar_ID_108955 Human_SNP_ID_624657806 m1A Human chr17 - 42536313 42536313 42536313 CGTCGCCTGCCGCGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCACCGCCGCGGCCACCGCCACC CGTCGCCTGCCGCGCCCCCGGCCCCGGCCAGGGGAAGGACCCCCACCGCCGCGGCCACCGCCACC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:42536275..42536425 26863196 MeRIP-seq:(Medium) rs957939258 Functional Loss SNV dbSNP153 33..33 33 - - - 108956 RMVar_ID_108956 Human_SNP_ID_624657807 m1A Human chr17 - 42536316 42536316 42536316 CCTCGTCGCCTGCCGCGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCACCGCCGCGGCCACCGCC CCTCGTCGCCTGCCGCGCCCCCGGCCCCGGCCGGGAGAAGGACCCCCACCGCCGCGGCCACCGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42536272..42536946 26863196 MeRIP-seq:(Medium) rs1280690494 Functional Loss SNV dbSNP153 33..33 33 - - - 108957 RMVar_ID_108957 Human_SNP_ID_624657834 m1A Human chr17 + 42536398 42536398 42536398 GTGCGGGCGCTCGTGGCCCGGCTGCTGGGGCCAGGCCCCGCGGCCGACTTCTCCGTGTCGGTGGA GTGCGGGCGCTCGTGGCCCGGCTGCTGGGGCCGGGCCCCGCGGCCGACTTCTCCGTGTCGGTGGA A G NAGLU Ensembl:ENSG00000108784 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42536299..42538341 26863410 MeRIP-seq:(Medium) rs1463936178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464551,Human_RBP_ID_22443672 108958 RMVar_ID_108958 Human_SNP_ID_624659301 m1A Human chr17 + 42541039 42541039 42541039 CTACTCCTGCTCCTTCCTTCTGGCTCCGGAAGACCCCATATTCCCCATCATCGGGAGCCTCTTCC CTACTCCTGCTCCTTCCTTCTGGCTCCGGAAGTCCCCATATTCCCCATCATCGGGAGCCTCTTCC A T AC067852.1,NAGLU Ensembl:ENSG00000266929,Ensembl:ENSG00000108784 lincRNA,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42540988..42541223 26863196 MeRIP-seq:(Medium) rs1438953428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18697926,Human_RBP_ID_22444609 Human_Splice_Rec_1819636,Human_Splice_Rec_1819644 RMVar_hsa_circ_184401,RMVar_hsa_circ_184399,RMVar_hsa_circ_117429,RMVar_hsa_circ_273151,RMVar_hsa_circ_113956,RMVar_hsa_circ_184402,RMVar_hsa_circ_82473,RMVar_hsa_circ_287635,RMVar_hsa_circ_184403 108959 RMVar_ID_108959 Human_SNP_ID_624663586 m1A Human chr17 - 42554601 42554601 42554601 CGCGCCGGAGGACGCACCGCCCCCACTCCTGGAGTCCAGCCCGGCGCTCACCTCCGCCACCTCCT CGCGCCGGAGGACGCACCGCCCCCACTCCTGGGGTCCAGCCCGGCGCTCACCTCCGCCACCTCCT T C AC067852.2 Ensembl:ENSG00000266962 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42554550..42554766 26863196 MeRIP-seq:(Medium) rs746209407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901562,Human_RBP_ID_23118896 Human_miRNA_ID_3176008,Human_miRNA_ID_3181769,Human_miRNA_ID_3181882,Human_miRNA_ID_3181997,Human_miRNA_ID_3182108,Human_miRNA_ID_3182222,Human_miRNA_ID_3182336,Human_miRNA_ID_3182654,Human_miRNA_ID_3182765,Human_miRNA_ID_3184543,Human_miRNA_ID_3208637 108960 RMVar_ID_108960 Human_SNP_ID_624663587 m1A Human chr17 - 42554601 42554601 42554601 CGCGCCGGAGGACGCACCGCCCCCACTCCTGGAGTCCAGCCCGGCGCTCACCTCCGCCACCTCCT CGCGCCGGAGGACGCACCGCCCCCACTCCTGGCGTCCAGCCCGGCGCTCACCTCCGCCACCTCCT T G AC067852.2 Ensembl:ENSG00000266962 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42554550..42554766 26863196 MeRIP-seq:(Medium) rs746209407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901562,Human_RBP_ID_23118896 Human_miRNA_ID_3176008,Human_miRNA_ID_3181769,Human_miRNA_ID_3181882,Human_miRNA_ID_3181997,Human_miRNA_ID_3182108,Human_miRNA_ID_3182222,Human_miRNA_ID_3182336,Human_miRNA_ID_3182654,Human_miRNA_ID_3182765,Human_miRNA_ID_3184543,Human_miRNA_ID_3208637 108961 RMVar_ID_108961 Human_SNP_ID_624665816 m1A Human chr17 - 42562471 42562471 42562471 GGGTTTCAGTGCTGACCGACAGGAGCCGGGGGAGGGGACGGGGCCTGGTAGACGGCGCCTCGGGG GGGTTTCAGTGCTGACCGACAGGAGCCGGGGGGGGGGACGGGGCCTGGTAGACGGCGCCTCGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42562151..42563232 26863196 MeRIP-seq:(Medium) rs762180459 Functional Loss SNV dbSNP153 33..33 33 - - - 108962 RMVar_ID_108962 Human_SNP_ID_624665817 m1A Human chr17 - 42562471 42562471 42562471 GGGTTTCAGTGCTGACCGACAGGAGCCGGGGGAGGGGACGGGGCCTGGTAGACGGCGCCTCGGGG GGGTTTCAGTGCTGACCGACAGGAGCCGGGGGCGGGGACGGGGCCTGGTAGACGGCGCCTCGGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42562151..42563232 26863196 MeRIP-seq:(Medium) rs762180459 Functional Loss SNV dbSNP153 33..33 33 - - - 108963 RMVar_ID_108963 Human_SNP_ID_624665900 m1A Human chr17 - 42562654 42562654 42562654 GGCGAGGGGCTAGGGAGGCCAGCGGCGTCGTCAGCACCAGGAGACCCGACCGGAATACGGCCATG GGCGAGGGGCTAGGGAGGCCAGCGGCGTCGTCCGCACCAGGAGACCCGACCGGAATACGGCCATG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:42562229..42562825;chr17:42562151..42562925 26863196 MeRIP-seq:(Medium) rs1158901296 Functional Loss SNV dbSNP153 33..33 33 - - - 108964 RMVar_ID_108964 Human_SNP_ID_624665922 m1A Human chr17 + 42562695 42562695 42562695 CGCTGGCCTCCCTAGCCCCTCGCCTGGCCTCCATCCTGACCTCGGCGGCCCGGCTGGTGAATCAC CGCTGGCCTCCCTAGCCCCTCGCCTGGCCTCCCTCCTGACCTCGGCGGCCCGGCTGGTGAATCAC A C COASY Ensembl:ENSG00000068120 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42562176..42562878 26863410 MeRIP-seq:(Medium) rs765396519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819826,Human_RBP_ID_4428120,Human_RBP_ID_5466500,Human_RBP_ID_8452765,Human_RBP_ID_22057092,Human_RBP_ID_27254375 Human_Splice_Rec_1819712,Human_Splice_Rec_1819714,Human_Splice_Rec_1819716,Human_Splice_Rec_1819760,Human_Splice_Rec_1819762,Human_Splice_Rec_1819768 108965 RMVar_ID_108965 Human_SNP_ID_624665923 m1A Human chr17 + 42562695 42562695 42562695 CGCTGGCCTCCCTAGCCCCTCGCCTGGCCTCCATCCTGACCTCGGCGGCCCGGCTGGTGAATCAC CGCTGGCCTCCCTAGCCCCTCGCCTGGCCTCCGTCCTGACCTCGGCGGCCCGGCTGGTGAATCAC A G COASY Ensembl:ENSG00000068120 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42562176..42562878 26863410 MeRIP-seq:(Medium) rs765396519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819826,Human_RBP_ID_4428120,Human_RBP_ID_5466500,Human_RBP_ID_8452765,Human_RBP_ID_22057092,Human_RBP_ID_27254375 Human_Splice_Rec_1819712,Human_Splice_Rec_1819714,Human_Splice_Rec_1819716,Human_Splice_Rec_1819760,Human_Splice_Rec_1819762,Human_Splice_Rec_1819768 108966 RMVar_ID_108966 Human_SNP_ID_624666028 m1A Human chr17 + 42562867 42562867 42562867 CTATGCTGGCGCCGACGTCCACAGGCACTTGGACGTCAGAATCCTACTGACCAATATCCGAACCA CTATGCTGGCGCCGACGTCCACAGGCACTTGGGCGTCAGAATCCTACTGACCAATATCCGAACCA A G COASY Ensembl:ENSG00000068120 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42562816..42562954 26863196 MeRIP-seq:(Medium) rs779780364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489750,Human_RBP_ID_1534034,Human_RBP_ID_18943200,Human_RBP_ID_22062126 108967 RMVar_ID_108967 Human_SNP_ID_624666496 m1A Human chr17 + 42564178 42564178 42564178 ATGGCCATCAACCGCTTCCGCCTTGAGAATGTAACCCCTGAGGGAGACTGGCAGAGGGAGTGGAT ATGGCCATCAACCGCTTCCGCCTTGAGAATGTCACCCCTGAGGGAGACTGGCAGAGGGAGTGGAT A C COASY Ensembl:ENSG00000068120 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42564175..42564330 26863196 MeRIP-seq:(Medium) rs111775750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489761,Human_RBP_ID_19082680 108968 RMVar_ID_108968 Human_SNP_ID_624666999 m1A Human chr17 - 42565451 42565451 42565451 CACACACGCTTTCCTGTGGGGAGACCCCAGTCACCGCCAGCAGTGCCGACGTTCTCCCAGGCAGA CACACACGCTTTCCTGTGGGGAGACCCCAGTCTCCGCCAGCAGTGCCGACGTTCTCCCAGGCAGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42565445..42565564 26863196 MeRIP-seq:(Medium) rs776691372 Functional Loss SNV dbSNP153 33..33 33 - - - 108969 RMVar_ID_108969 Human_SNP_ID_624667803 m1A Human chr17 - 42567620 42567620 42567620 GGTCCAGGCTGTTGTCGCTGTAGGCATACTCCACCTGCGGCACAGAGCACGGGAAGGGCCCGTCA GGTCCAGGCTGTTGTCGCTGTAGGCATACTCCGCCTGCGGCACAGAGCACGGGAAGGGCCCGTCA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42567601..42567675 26863410 MeRIP-seq:(Medium) rs1367200651 Functional Loss SNV dbSNP153 33..33 33 - - - 108970 RMVar_ID_108970 Human_SNP_ID_624667807 m1A Human chr17 + 42567638 42567638 42567638 CTCTGTGCCGCAGGTGGAGTATGCCTACAGCGACAACAGCCTGGACCCCGGTGAGTAGCTGCCCC CTCTGTGCCGCAGGTGGAGTATGCCTACAGCGGCAACAGCCTGGACCCCGGTGAGTAGCTGCCCC A G MLX Ensembl:ENSG00000108788 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42567601..42567675 26863196 MeRIP-seq:(Medium) rs1433297005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489774,Human_RBP_ID_822466,Human_RBP_ID_900052,Human_RBP_ID_5144191,Human_RBP_ID_9376038,Human_RBP_ID_19079145,Human_RBP_ID_22543294 Human_Splice_Rec_1819801,Human_Splice_Rec_1819814,Human_Splice_Rec_1819815,Human_Splice_Rec_1819827,Human_Splice_Rec_1819837,Human_Splice_Rec_1819846,Human_Splice_Rec_1819847,Human_Splice_Rec_1819855,Human_Splice_Rec_1819859,Human_Splice_Rec_1819866,Human_Splice_Rec_1819867,Human_Splice_Rec_1819872,Human_Splice_Rec_1819873 RMVar_hsa_circ_81872,RMVar_hsa_circ_97185,RMVar_hsa_circ_184406,RMVar_hsa_circ_184407 108971 RMVar_ID_108971 Human_SNP_ID_624669609 m1A Human chr17 + 42573140 42573140 42573140 AAGAACTGCTTCTTGCTCTTGGGGTATCCTTCAAGTATTGCATCAGACAGCTCTGTAGCCTGACA AAGAACTGCTTCTTGCTCTTGGGGTATCCTTCCAGTATTGCATCAGACAGCTCTGTAGCCTGACA A C MLX Ensembl:ENSG00000108788 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42573138..42573643 32194978 MeRIP-seq:(Medium) rs138687177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1534093 108972 RMVar_ID_108972 Human_SNP_ID_624669610 m1A Human chr17 + 42573140 42573140 42573140 AAGAACTGCTTCTTGCTCTTGGGGTATCCTTCAAGTATTGCATCAGACAGCTCTGTAGCCTGACA AAGAACTGCTTCTTGCTCTTGGGGTATCCTTCGAGTATTGCATCAGACAGCTCTGTAGCCTGACA A G MLX Ensembl:ENSG00000108788 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42573138..42573643 32194978 MeRIP-seq:(Medium) rs138687177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1534093 108973 RMVar_ID_108973 Human_SNP_ID_624669706 m1A Human chr17 + 42573361 42573361 42573361 CCACTCCTTACAGTACTTCTGCCTCTCTCTGTACACCTAGAAGGAAAAAGCAAGTTCCTCTAACT CCACTCCTTACAGTACTTCTGCCTCTCTCTGTTCACCTAGAAGGAAAAAGCAAGTTCCTCTAACT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42573006..42573643 26863196 MeRIP-seq:(Medium) rs2292754 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_20215973 108974 RMVar_ID_108974 Human_SNP_ID_624669760 m1A Human chr17 - 42573482 42573480 42573482 AGCTACCAATCATGTGACTCCAGAAGAGAAAGAGCAGGTGAGCTGGAAGGCTGTAGGACCGCTGT AGCTACCAATCATGTGACTCCAGAAGAGAAAG__CAGGTGAGCTGGAAGGCTGTAGGACCGCTGT GCT G PSMC3IP Ensembl:ENSG00000131470 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42573006..42573618 26863196 MeRIP-seq:(Medium) rs765972932 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3952439,Human_RBP_ID_6595692,Human_RBP_ID_13009627,Human_RBP_ID_18991357,Human_RBP_ID_26333373 Human_Splice_Rec_1819891,Human_Splice_Rec_1819905,Human_Splice_Rec_1819917,Human_Splice_Rec_1819933,Human_Splice_Rec_1819945,Human_Splice_Rec_1819957,Human_Splice_Rec_1819971,Human_Splice_Rec_1819985 108975 RMVar_ID_108975 Human_SNP_ID_624670051 m1A Human chr17 + 42574202 42574202 42574202 AGGACTTGAAGGTCAGCATCACTCACCATGTCAAACTGGTCCTGCCAGACAAAGAGGGAAAATAC AGGACTTGAAGGTCAGCATCACTCACCATGTCCAACTGGTCCTGCCAGACAAAGAGGGAAAATAC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42574151..42574225 26863196 MeRIP-seq:(Medium) rs907079384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20216007 108976 RMVar_ID_108976 Human_SNP_ID_624670052 m1A Human chr17 + 42574203 42574203 42574203 GGACTTGAAGGTCAGCATCACTCACCATGTCAAACTGGTCCTGCCAGACAAAGAGGGAAAATACA GGACTTGAAGGTCAGCATCACTCACCATGTCAGACTGGTCCTGCCAGACAAAGAGGGAAAATACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42574087..42576684 26863196 MeRIP-seq:(Medium) rs1450988899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20216007 108977 RMVar_ID_108977 Human_SNP_ID_624671087 m1A Human chr17 - 42577649 42577649 42577649 TAAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAACGGCGCCGTGGGCGCGGGGAAGACCCGGGAGG TAAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAGCGGCGCCGTGGGCGCGGGGAAGACCCGGGAGG T C PSMC3IP Ensembl:ENSG00000131470 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42577443..42577734 26863196 MeRIP-seq:(Medium) rs764111327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18419958,Human_RBP_ID_18988513,Human_RBP_ID_19082705,Human_RBP_ID_27838451 RMVar_hsa_circ_98110,RMVar_hsa_circ_184413 108978 RMVar_ID_108978 Human_SNP_ID_624671092 m1A Human chr17 - 42577654 42577654 42577654 ATGAGTAAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAACGGCGCCGTGGGCGCGGGGAAGACCCG ATGAGTAAAGGCCGGGCAGAAGCTGCGGCGGGGGGTAACGGCGCCGTGGGCGCGGGGAAGACCCG T C PSMC3IP Ensembl:ENSG00000131470 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr17:42577451..42577700;chr17:42577201..42577725 26863196 MeRIP-seq:(Medium) rs1329547831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_900057,Human_RBP_ID_4467245,Human_RBP_ID_18419958,Human_RBP_ID_18988513,Human_RBP_ID_27812711,Human_RBP_ID_27838451 Human_Splice_Rec_1819883,Human_Splice_Rec_1819897,Human_Splice_Rec_1819923,Human_Splice_Rec_1819951,Human_Splice_Rec_1819963,Human_Splice_Rec_1819977 RMVar_hsa_circ_98110,RMVar_hsa_circ_184413 108979 RMVar_ID_108979 Human_SNP_ID_624671104 m1A Human chr17 - 42577680 42577680 42577680 TTCTGAGTTGGGTGGCGGGAAAGGCGATGAGTAAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAAC TTCTGAGTTGGGTGGCGGGAAAGGCGATGAGTGAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAAC T C PSMC3IP Ensembl:ENSG00000131470 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:42577568..42577697 26863196 MeRIP-seq:(Medium) rs373107959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489823,Human_RBP_ID_4428311,Human_RBP_ID_18419958,Human_RBP_ID_18988513,Human_RBP_ID_23726876,Human_RBP_ID_27812711,Human_RBP_ID_27838451 Human_Splice_Rec_1819883,Human_Splice_Rec_1819897,Human_Splice_Rec_1819923,Human_Splice_Rec_1819951,Human_Splice_Rec_1819963,Human_Splice_Rec_1819977 RMVar_hsa_circ_98110,RMVar_hsa_circ_184413 108980 RMVar_ID_108980 Human_SNP_ID_624680060 m1A Human chr17 + 42609734 42609734 42609734 GGCGGGAGCGGCTGCAACGCCGGTGCCTGAGGAGCGATGCCGAGGGAAATCATCACCCTACAGTT GGCGGGAGCGGCTGCAACGCCGGTGCCTGAGGGGCGATGCCGAGGGAAATCATCACCCTACAGTT A G TUBG1 Ensembl:ENSG00000131462 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42609651..42610573 26863196 MeRIP-seq:(Medium) rs765712365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236135,Human_RBP_ID_765209,Human_RBP_ID_820684,Human_RBP_ID_4428451,Human_RBP_ID_8818135,Human_RBP_ID_23726948,Human_RBP_ID_27254450 Human_Splice_Rec_1820105,Human_Splice_Rec_1820125,Human_Splice_Rec_1820131,Human_Splice_Rec_1820145,Human_Splice_Rec_1820163 RMVar_hsa_circ_91736,RMVar_hsa_circ_184420 108981 RMVar_ID_108981 Human_SNP_ID_624680065 m1A Human chr17 + 42609738 42609738 42609738 GGAGCGGCTGCAACGCCGGTGCCTGAGGAGCGATGCCGAGGGAAATCATCACCCTACAGTTGGGC GGAGCGGCTGCAACGCCGGTGCCTGAGGAGCGTTGCCGAGGGAAATCATCACCCTACAGTTGGGC A T TUBG1 Ensembl:ENSG00000131462 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42609651..42610573 26863196 MeRIP-seq:(Medium) rs1367246438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236135,Human_RBP_ID_765209,Human_RBP_ID_820684,Human_RBP_ID_1534117,Human_RBP_ID_4428451,Human_RBP_ID_8818135,Human_RBP_ID_23726948 Human_Splice_Rec_1820105,Human_Splice_Rec_1820125,Human_Splice_Rec_1820131,Human_Splice_Rec_1820145,Human_Splice_Rec_1820163 RMVar_hsa_circ_91736,RMVar_hsa_circ_184420 108982 RMVar_ID_108982 Human_SNP_ID_624681198 m1A Human chr17 + 42613936 42613936 42613936 ACAATGACCTCATCGGCCTCATCGCCTCGCTCATTCCCACCCCACGGCTCCACTTCCTCATGACC ACAATGACCTCATCGGCCTCATCGCCTCGCTCGTTCCCACCCCACGGCTCCACTTCCTCATGACC A G TUBG1 Ensembl:ENSG00000131462 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:42613736..42613935 26863410 MeRIP-seq:(Medium) rs1399630499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4428473,Human_RBP_ID_22951550 Human_Splice_Rec_1820118,Human_Splice_Rec_1820119,Human_Splice_Rec_1820144,Human_Splice_Rec_1820156,Human_Splice_Rec_1820157 Human_miRNA_ID_99354 RMVar_hsa_circ_100005,RMVar_hsa_circ_91736,RMVar_hsa_circ_112375,RMVar_hsa_circ_184420,RMVar_hsa_circ_184421,RMVar_hsa_circ_184422,RMVar_hsa_circ_90826,RMVar_hsa_circ_184424,RMVar_hsa_circ_109542,RMVar_hsa_circ_77996,RMVar_hsa_circ_80064,RMVar_hsa_circ_184426,RMVar_hsa_circ_184427,RMVar_hsa_circ_184428,RMVar_hsa_circ_184429,RMVar_hsa_circ_114204,RMVar_hsa_circ_184430,RMVar_hsa_circ_184431 108983 RMVar_ID_108983 Human_SNP_ID_624681199 m1A Human chr17 + 42613947 42613938 42613947 ATCGGCCTCATCGCCTCGCTCATTCCCACCCCACGGCTCCACTTCCTCATGACCGGCTACACCCC ATCGGCCTCATCGCCTCGCTCATT_________CGGCTCCACTTCCTCATGACCGGCTACACCCC TCCCACCCCA T TUBG1 Ensembl:ENSG00000131462 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42613730..42613975 26863410 MeRIP-seq:(Medium) rs1315549058 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_4428474,Human_RBP_ID_17378738,Human_RBP_ID_18943204 Human_Splice_Rec_1820118,Human_Splice_Rec_1820119,Human_Splice_Rec_1820144,Human_Splice_Rec_1820156,Human_Splice_Rec_1820157 Human_miRNA_ID_99354 RMVar_hsa_circ_100005,RMVar_hsa_circ_91736,RMVar_hsa_circ_112375,RMVar_hsa_circ_184420,RMVar_hsa_circ_184421,RMVar_hsa_circ_184422,RMVar_hsa_circ_90826,RMVar_hsa_circ_184424,RMVar_hsa_circ_109542,RMVar_hsa_circ_77996,RMVar_hsa_circ_80064,RMVar_hsa_circ_184426,RMVar_hsa_circ_184427,RMVar_hsa_circ_184428,RMVar_hsa_circ_184429,RMVar_hsa_circ_114204,RMVar_hsa_circ_184430,RMVar_hsa_circ_184431 108984 RMVar_ID_108984 Human_SNP_ID_624681308 m1A Human chr17 - 42614254 42614254 42614254 GACCGTGGTCTTCCTCACGCTGGCCACCTGATAGGACAGTGAGACAGGGACCCGGCCAGCGCTCA GACCGTGGTCTTCCTCACGCTGGCCACCTGATGGGACAGTGAGACAGGGACCCGGCCAGCGCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42614251..42614300 26863196 MeRIP-seq:(Medium) rs521358 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_704 108985 RMVar_ID_108985 Human_SNP_ID_624692766 m1A Human chr17 - 42660754 42660754 42660754 CTATCCAGGCCACCTCCTGACCTGTCCCCAGCACTCTTCGGCCTCCCTGCCCATTCCTTCCCCCA CTATCCAGGCCACCTCCTGACCTGTCCCCAGCTCTCTTCGGCCTCCCTGCCCATTCCTTCCCCCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42660722..42660813 26863196 MeRIP-seq:(Medium) rs777512206 Functional Loss SNV dbSNP153 33..33 33 - - - 108986 RMVar_ID_108986 Human_SNP_ID_624695187 m1A Human chr17 - 42669227 42669227 42669227 AATCCCAGGCTATGAAGACAGTGAGAAATGCTACAAAGGAAAGAGTGATGTGACAGGAAGCCAGG AATCCCAGGCTATGAAGACAGTGAGAAATGCTGCAAAGGAAAGAGTGATGTGACAGGAAGCCAGG T C PLEKHH3 Ensembl:ENSG00000068137 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42669182..42669458 26863196 MeRIP-seq:(Medium) rs182905041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96929,RMVar_hsa_circ_184441 108987 RMVar_ID_108987 Human_SNP_ID_624695390 m1A Human chr17 - 42669814 42669814 42669814 CACGGAGTGTCACGTAATTCCCCACATCCAGAACAGCTACCCATCTCAAACCCCAGGAGTCACCA CACGGAGTGTCACGTAATTCCCCACATCCAGAGCAGCTACCCATCTCAAACCCCAGGAGTCACCA T C PLEKHH3 Ensembl:ENSG00000068137 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42669801..42669982 26863196 MeRIP-seq:(Medium) rs1567955842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_764406,Human_RBP_ID_896546,Human_RBP_ID_5362811,Human_RBP_ID_17079600,Human_RBP_ID_22656328 RMVar_hsa_circ_96929,RMVar_hsa_circ_184441 108988 RMVar_ID_108988 Human_SNP_ID_624696624 m1A Human chr17 + 42673208 42673208 42673208 CTGGGGCGCTGACTCCATAGGGCAGGGGCAGGAGTGGGGCATACAAGGCTCCACTAGTGTGTCTC CTGGGGCGCTGACTCCATAGGGCAGGGGCAGGGGTGGGGCATACAAGGCTCCACTAGTGTGTCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42673183..42673292 26863196 MeRIP-seq:(Medium) rs948057261 Functional Loss SNV dbSNP153 33..33 33 - - - 108989 RMVar_ID_108989 Human_SNP_ID_624697771 m1A Human chr17 + 42676851 42676849 42676851 AATGTCCGGAGCTGGGAAGTAGTGTCCGTTGGAGTGTCCAGCCCTGTGGGGGGCAGTGTCCGGTG AATGTCCGGAGCTGGGAAGTAGTGTCCGTTG__GTGTCCAGCCCTGTGGGGGGCAGTGTCCGGTG GGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42676801..42676961 26863196 MeRIP-seq:(Medium) rs780039619 Functional Loss DEL dbSNP153 32..33 33 - - - 108990 RMVar_ID_108990 Human_SNP_ID_624697774 m1A Human chr17 + 42676851 42676851 42676851 AATGTCCGGAGCTGGGAAGTAGTGTCCGTTGGAGTGTCCAGCCCTGTGGGGGGCAGTGTCCGGTG AATGTCCGGAGCTGGGAAGTAGTGTCCGTTGGCGTGTCCAGCCCTGTGGGGGGCAGTGTCCGGTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42676801..42676961 26863196 MeRIP-seq:(Medium) rs1180344367 Functional Loss SNV dbSNP153 33..33 33 - - - 108991 RMVar_ID_108991 Human_SNP_ID_624699442 m1A Human chr17 + 42682632 42682632 42682632 GAGGATAGAGAGAGAAGAGCGGAGGACCAGGAACCAGAGAGAGAGAGAGAGAAAAGAGAGAGGAG GAGGATAGAGAGAGAAGAGCGGAGGACCAGGAGCCAGAGAGAGAGAGAGAGAAAAGAGAGAGGAG A G CNTNAP1 Ensembl:ENSG00000108797 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:42682526..42683837;chr17:42682500..42684050;chr17:42682514..42682824 26863196 MeRIP-seq:(Medium) rs1017347979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4428601 108992 RMVar_ID_108992 Human_SNP_ID_624699449 m1A Human chr17 + 42682643 42682643 42682643 GAGAAGAGCGGAGGACCAGGAACCAGAGAGAGAGAGAGAGAAAAGAGAGAGGAGAGACAGAGCGC GAGAAGAGCGGAGGACCAGGAACCAGAGAGAGGGAGAGAGAAAAGAGAGAGGAGAGACAGAGCGC A G CNTNAP1 Ensembl:ENSG00000108797 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42682528..42683837 26863196 MeRIP-seq:(Medium) rs1028330676 Functional Loss SNV dbSNP153 33..33 33 - - - 108993 RMVar_ID_108993 Human_SNP_ID_624700929 m1A Human chr17 + 42687116 42687116 42687116 AAGCGTCGTGGAAAGCAAAGAGGTGGAGCGGGAAGAGATATTGAACATCAGATAAAAGCGGAGAA AAGCGTCGTGGAAAGCAAAGAGGTGGAGCGGGGAGAGATATTGAACATCAGATAAAAGCGGAGAA A G CNTNAP1 Ensembl:ENSG00000108797 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42687065..42687287 26863196 MeRIP-seq:(Medium) rs918187224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896553 RMVar_hsa_circ_268834,RMVar_hsa_circ_184444,RMVar_hsa_circ_288901 108994 RMVar_ID_108994 Human_SNP_ID_624700930 m1A Human chr17 + 42687121 42687121 42687121 TCGTGGAAAGCAAAGAGGTGGAGCGGGAAGAGATATTGAACATCAGATAAAAGCGGAGAATCCCT TCGTGGAAAGCAAAGAGGTGGAGCGGGAAGAGTTATTGAACATCAGATAAAAGCGGAGAATCCCT A T CNTNAP1 Ensembl:ENSG00000108797 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42687071..42687212 26863196 MeRIP-seq:(Medium) rs140555488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896553 RMVar_hsa_circ_268834,RMVar_hsa_circ_184444,RMVar_hsa_circ_288901 108995 RMVar_ID_108995 Human_SNP_ID_624704280 m1A Human chr17 - 42698780 42698780 42698780 GAGCTTGGTTGGGAGCTGCTGTAGGGGTGGGGACCTGGGCAGGGCCTGAAGTGGGTAGGGGAGGT GAGCTTGGTTGGGAGCTGCTGTAGGGGTGGGGCCCTGGGCAGGGCCTGAAGTGGGTAGGGGAGGT T G AC100793.3 Ensembl:ENSG00000267765 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42698733..42698825 26863196 MeRIP-seq:(Medium) rs570981828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_200554 Clinvar_Rec_705,Clinvar_Rec_706 108996 RMVar_ID_108996 Human_SNP_ID_624715241 m1A Human chr17 + 42744724 42744724 42744724 GGGCTCCCGCCCACCGGCCCACACCGCCATCCAACGGGATTCCCCGTCCCCGAGCCCGCCCCCGC GGGCTCCCGCCCACCGGCCCACACCGCCATCCGACGGGATTCCCCGTCCCCGAGCCCGCCCCCGC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:42744716..42744919 26863196 MeRIP-seq:(Medium) rs1387178739 Functional Loss SNV dbSNP153 33..33 33 - - - 108997 RMVar_ID_108997 Human_SNP_ID_624715297 m1A Human chr17 + 42744903 42744903 42744903 ACCCCCGGCCAGGCAGGCAGTGTGTCCCTCGGATTCCTTCCAATTTCCTGATCCCTCCGCCTCTC ACCCCCGGCCAGGCAGGCAGTGTGTCCCTCGGGTTCCTTCCAATTTCCTGATCCCTCCGCCTCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42744590..42745021 26863196 MeRIP-seq:(Medium) rs995913909 Functional Loss SNV dbSNP153 33..33 33 - - - 108998 RMVar_ID_108998 Human_SNP_ID_624715336 m1A Human chr17 + 42744991 42744991 42744991 AGGGGAGGAGGCCCGGCCCCACCGCCCGGCCCAGGCTTGTTTACTCACTCACCCTCCATCCCGAG AGGGGAGGAGGCCCGGCCCCACCGCCCGGCCCCGGCTTGTTTACTCACTCACCCTCCATCCCGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42744399..42745003 26863196 MeRIP-seq:(Medium) rs962611522 Functional Loss SNV dbSNP153 33..33 33 - - - 108999 RMVar_ID_108999 Human_SNP_ID_624722440 m1A Human chr17 - 42773807 42773807 42773807 CTTCCATCACCGTCATGCTGGACTGTTTGTGCAGGCGGCAGAAGGACAGGACCAGCGAGCACCAG CTTCCATCACCGTCATGCTGGACTGTTTGTGCGGGCGGCAGAAGGACAGGACCAGCGAGCACCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42773726..42773926 32194978 MeRIP-seq:(Medium) rs1380494585 Functional Loss SNV dbSNP153 33..33 33 - - - 109000 RMVar_ID_109000 Human_SNP_ID_624728303 m1A Human chr17 + 42795054 42795052 42795054 CAGCACACCCGAGTTTCCGGTCCCACTCTCTCAGTGTCCCTGGAGTTCTCTCCCCACGACTTCTC CAGCACACCCGAGTTTCCGGTCCCACTCTCT__GTGTCCCTGGAGTTCTCTCCCCACGACTTCTC TCA T WNK4 Ensembl:ENSG00000126562 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42795004..42795161;chr17:42795004..42795187 26863196 MeRIP-seq:(Medium) rs1388075542 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1286484,Human_RBP_ID_5129164,Human_RBP_ID_13011303,Human_RBP_ID_17080050,Human_RBP_ID_17375757,Human_RBP_ID_18943218,Human_RBP_ID_20216596 109001 RMVar_ID_109001 Human_SNP_ID_624728305 m1A Human chr17 + 42795092 42795065 42795093 CCTGGAGTTCTCTCCCCACGACTTCTCCACCTACGTTCTCTCCCACTTGTTCTCAGGTCACTCTT CCTGGA____________________________GTTCTCTCCCACTTGTTCTCAGGTCACTCTT AGTTCTCTCCCCACGACTTCTCCACCTAC A WNK4 Ensembl:ENSG00000126562 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42795043..42795133 26863196 MeRIP-seq:(Medium) rs1330496006 Functional Loss DEL dbSNP153 7..34 33 - - - Human_RBP_ID_1534186,Human_RBP_ID_17080277,Human_RBP_ID_18943218,Human_RBP_ID_20216598,Human_RBP_ID_22804614 109002 RMVar_ID_109002 Human_SNP_ID_624728318 m1A Human chr17 + 42795092 42795092 42795092 CCTGGAGTTCTCTCCCCACGACTTCTCCACCTACGTTCTCTCCCACTTGTTCTCAGGTCACTCTT CCTGGAGTTCTCTCCCCACGACTTCTCCACCTGCGTTCTCTCCCACTTGTTCTCAGGTCACTCTT A G WNK4 Ensembl:ENSG00000126562 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42795043..42795133 26863196 MeRIP-seq:(Medium) rs141615112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1534186,Human_RBP_ID_17080277,Human_RBP_ID_18943218,Human_RBP_ID_20216598,Human_RBP_ID_22804614 109003 RMVar_ID_109003 Human_SNP_ID_624729252 m1A Human chr17 - 42798049 42798049 42798049 GCAAGGGCGTCAGGGTCCTAATCTGGATGGGTATTGATCATGTCCAACCTGCTGGAGCCCCTTCA GCAAGGGCGTCAGGGTCCTAATCTGGATGGGTGTTGATCATGTCCAACCTGCTGGAGCCCCTTCA T C COA3 Ensembl:ENSG00000183978 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42797861..42798175 32194978 MeRIP-seq:(Medium) rs1379026442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6358,Human_RBP_ID_132126,Human_RBP_ID_489978,Human_RBP_ID_766499,Human_RBP_ID_5114686,Human_RBP_ID_17654195,Human_RBP_ID_22443693,Human_RBP_ID_22499503 Human_miRNA_ID_2486458,Human_miRNA_ID_3074823 RMVar_hsa_circ_88355,RMVar_hsa_circ_95848,RMVar_hsa_circ_184499,RMVar_hsa_circ_184500 109004 RMVar_ID_109004 Human_SNP_ID_624729468 m1A Human chr17 - 42798611 42798611 42798611 GCGTGGAGAGGCCCCGTTCGCTCAGCGTATCGACCCGACTCGGGAGAAGCTGACACCCGAGCAAC GCGTGGAGAGGCCCCGTTCGCTCAGCGTATCGGCCCGACTCGGGAGAAGCTGACACCCGAGCAAC T C COA3 Ensembl:ENSG00000183978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42798451..42798700 26863410 MeRIP-seq:(Medium) rs762393307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767531,Human_RBP_ID_902403,Human_RBP_ID_4465417,Human_RBP_ID_17654731,Human_RBP_ID_22444630,Human_RBP_ID_24371751,Human_RBP_ID_27452619 RMVar_hsa_circ_95848,RMVar_hsa_circ_184500 109005 RMVar_ID_109005 Human_SNP_ID_624729469 m1A Human chr17 - 42798611 42798611 42798611 GCGTGGAGAGGCCCCGTTCGCTCAGCGTATCGACCCGACTCGGGAGAAGCTGACACCCGAGCAAC GCGTGGAGAGGCCCCGTTCGCTCAGCGTATCGCCCCGACTCGGGAGAAGCTGACACCCGAGCAAC T G COA3 Ensembl:ENSG00000183978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:42798451..42798700 26863410 MeRIP-seq:(Medium) rs762393307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767531,Human_RBP_ID_902403,Human_RBP_ID_4465417,Human_RBP_ID_17654731,Human_RBP_ID_22444630,Human_RBP_ID_24371751,Human_RBP_ID_27452619 RMVar_hsa_circ_95848,RMVar_hsa_circ_184500 109006 RMVar_ID_109006 Human_SNP_ID_624734511 m1A Human chr17 - 42818329 42818327 42818330 GATGGAGCTAAAGGAGCTGGCACTAGAGGAGGAGAGGCTGATCCAGGAGCTGGAAGACGTGGAAA GATGGAGCTAAAGGAGCTGGCACTAGAGGAG___AGGCTGATCCAGGAGCTGGAAGACGTGGAAA TCTC T BECN1 Ensembl:ENSG00000126581 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42818280..42818375 26863196 MeRIP-seq:(Medium) rs1438349098 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_237768,Human_RBP_ID_490012,Human_RBP_ID_6596131,Human_RBP_ID_9376056,Human_RBP_ID_13011542,Human_RBP_ID_23727097,Human_RBP_ID_26333390,Human_RBP_ID_27813915 Human_Splice_Rec_1821164,Human_Splice_Rec_1821182,Human_Splice_Rec_1821200,Human_Splice_Rec_1821222,Human_Splice_Rec_1821240,Human_Splice_Rec_1821252,Human_Splice_Rec_1821264,Human_Splice_Rec_1821292,Human_Splice_Rec_1821296 RMVar_hsa_circ_48256,RMVar_hsa_circ_296663,RMVar_hsa_circ_184502 109007 RMVar_ID_109007 Human_SNP_ID_624734513 m1A Human chr17 - 42818329 42818329 42818329 GATGGAGCTAAAGGAGCTGGCACTAGAGGAGGAGAGGCTGATCCAGGAGCTGGAAGACGTGGAAA GATGGAGCTAAAGGAGCTGGCACTAGAGGAGGGGAGGCTGATCCAGGAGCTGGAAGACGTGGAAA T C BECN1 Ensembl:ENSG00000126581 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42818280..42818375 26863196 MeRIP-seq:(Medium) rs1369571411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237768,Human_RBP_ID_490012,Human_RBP_ID_6596131,Human_RBP_ID_9376056,Human_RBP_ID_13011542,Human_RBP_ID_23727097,Human_RBP_ID_26333390,Human_RBP_ID_27813915 Human_Splice_Rec_1821164,Human_Splice_Rec_1821182,Human_Splice_Rec_1821200,Human_Splice_Rec_1821222,Human_Splice_Rec_1821240,Human_Splice_Rec_1821252,Human_Splice_Rec_1821264,Human_Splice_Rec_1821292,Human_Splice_Rec_1821296 RMVar_hsa_circ_48256,RMVar_hsa_circ_296663,RMVar_hsa_circ_184502 109008 RMVar_ID_109008 Human_SNP_ID_624735913 m1A Human chr17 - 42823852 42823852 42823852 CTCAGGGATGGAAGGGTCTAAGACGTCCAACAACAGCACCATGCAGGTGAGCTTCGTGTGCCAGC CTCAGGGATGGAAGGGTCTAAGACGTCCAACAGCAGCACCATGCAGGTGAGCTTCGTGTGCCAGC T C BECN1 Ensembl:ENSG00000126581 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42823801..42823921 26863196 MeRIP-seq:(Medium) rs774450039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903878,Human_RBP_ID_1534235,Human_RBP_ID_18988550 Human_Splice_Rec_1821156,Human_Splice_Rec_1821176,Human_Splice_Rec_1821192,Human_Splice_Rec_1821216,Human_Splice_Rec_1821234,Human_Splice_Rec_1821286,Human_Splice_Rec_1821300,Human_Splice_Rec_1821308,Human_Splice_Rec_1821314,Human_Splice_Rec_1821318,Human_Splice_Rec_1821326,Human_Splice_Rec_1821334 RMVar_hsa_circ_19588,RMVar_hsa_circ_184503,RMVar_hsa_circ_371155 109009 RMVar_ID_109009 Human_SNP_ID_624735921 m1A Human chr17 - 42823881 42823881 42823881 TCTCCCTAATGTTGCCTCTTTTCCACGGCCTCAGGGATGGAAGGGTCTAAGACGTCCAACAACAG TCTCCCTAATGTTGCCTCTTTTCCACGGCCTCGGGGATGGAAGGGTCTAAGACGTCCAACAACAG T C BECN1,MIR6781 Ensembl:ENSG00000126581,Ensembl:ENSG00000278447 Protein coding,miRNA intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42823846..42823936 26863196 MeRIP-seq:(Medium) rs1372148693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9072101 109010 RMVar_ID_109010 Human_SNP_ID_624738349 m1A Human chr17 + 42833453 42833453 42833453 AGCCGGGAGGGCGAGCGAGAGAGCAAGCAGGCAGCAGGCTGCCGGCGGGCGGGCGGACGGCACAG AGCCGGGAGGGCGAGCGAGAGAGCAAGCAGGCCGCAGGCTGCCGGCGGGCGGGCGGACGGCACAG A C PSME3 Ensembl:ENSG00000131467 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42833401..42833600 26863196 MeRIP-seq:(Medium) rs879596236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50574,Human_RBP_ID_4428840,Human_RBP_ID_9378275,Human_RBP_ID_21890124,Human_RBP_ID_26961729 Human_Splice_Rec_1821419 109011 RMVar_ID_109011 Human_SNP_ID_624738350 m1A Human chr17 + 42833453 42833453 42833453 AGCCGGGAGGGCGAGCGAGAGAGCAAGCAGGCAGCAGGCTGCCGGCGGGCGGGCGGACGGCACAG AGCCGGGAGGGCGAGCGAGAGAGCAAGCAGGCGGCAGGCTGCCGGCGGGCGGGCGGACGGCACAG A G PSME3 Ensembl:ENSG00000131467 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42833401..42833600 26863196 MeRIP-seq:(Medium) rs879596236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50574,Human_RBP_ID_4428840,Human_RBP_ID_9378275,Human_RBP_ID_21890124,Human_RBP_ID_26961729 Human_Splice_Rec_1821419 109012 RMVar_ID_109012 Human_SNP_ID_624738356 m1A Human chr17 - 42833460 42833460 42833460 CCTCCCTCTGTGCCGTCCGCCCGCCCGCCGGCAGCCTGCTGCCTGCTTGCTCTCTCGCTCGCCCT CCTCCCTCTGTGCCGTCCGCCCGCCCGCCGGCGGCCTGCTGCCTGCTTGCTCTCTCGCTCGCCCT T C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:42833428..42833525 26863410 MeRIP-seq:(Medium) rs996050597 Functional Loss SNV dbSNP153 33..33 33 - - - 109013 RMVar_ID_109013 Human_SNP_ID_624738686 m1A Human chr17 - 42834330 42834329 42834330 GCTCCCTGAAAGAATCAACCTAAAATTAACAAAGAGAGCAATTCAGTACCTGGGGACAGAGGTAA GCTCCCTGAAAGAATCAACCTAAAATTAACAA_GAGAGCAATTCAGTACCTGGGGACAGAGGTAA CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42834326..42834400 26863196 MeRIP-seq:(Medium) rs1481258732 Functional Loss DEL dbSNP153 33..33 33 - - - 109014 RMVar_ID_109014 Human_SNP_ID_624738771 m1A Human chr17 - 42834505 42834505 42834505 AAATTTGCCACCAAGTCTTCTGCCTAAGGAAGAGGGAAAATACAGCTGAATTAATATCTGTGGGA AAATTTGCCACCAAGTCTTCTGCCTAAGGAAGGGGGAAAATACAGCTGAATTAATATCTGTGGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:42834501..42834550 26863196 MeRIP-seq:(Medium) rs1167073460 Functional Loss SNV dbSNP153 33..33 33 - - - 109015 RMVar_ID_109015 Human_SNP_ID_624741241 m1A Human chr17 - 42843148 42843148 42843148 CATTACGATCCATGGGTGATAGGGTGAGGAGGAGGGGCAGTGGAACAGTCCAACAAACGAAACGG CATTACGATCCATGGGTGATAGGGTGAGGAGGTGGGGCAGTGGAACAGTCCAACAAACGAAACGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42843097..42843195 26863196 MeRIP-seq:(Medium) rs750474961 Functional Loss SNV dbSNP153 33..33 33 - - - 109016 RMVar_ID_109016 Human_SNP_ID_624770487 m1A Human chr17 + 42956208 42956208 42956208 AGCCACTCCACAGCCGTTCCTCACTTACCTGAAGGTCACTGAGATTGCTCACATGGGTCCCACAG AGCCACTCCACAGCCGTTCCTCACTTACCTGAGGGTCACTGAGATTGCTCACATGGGTCCCACAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:42956205..42956438 32194978 MeRIP-seq:(Medium) rs763733058 Functional Loss SNV dbSNP153 33..33 33 - - - 109017 RMVar_ID_109017 Human_SNP_ID_624771099 m1A Human chr17 + 42957970 42957970 42957970 AGGAGGAACTATCAAGGAAGAGGGAACAAGACAGCCAAAGGCCTTAAGGAAGAAAGAAGTAGCGC AGGAGGAACTATCAAGGAAGAGGGAACAAGACCGCCAAAGGCCTTAAGGAAGAAAGAAGTAGCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42957968..42958053 26863196 MeRIP-seq:(Medium) rs1024569003 Functional Loss SNV dbSNP153 33..33 33 - - - 109018 RMVar_ID_109018 Human_SNP_ID_624772065 m1A Human chr17 + 42961314 42961314 42961314 GATCAGCCTGTTCCCCACGGCGAGTCACTCTCAGCACAGAGATGTCATTGATTGTACCACGGTCA GATCAGCCTGTTCCCCACGGCGAGTCACTCTCCGCACAGAGATGTCATTGATTGTACCACGGTCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42961140..42962228 26863196 MeRIP-seq:(Medium) rs1451488614 Functional Loss SNV dbSNP153 33..33 33 - - - 109019 RMVar_ID_109019 Human_SNP_ID_624772636 m1A Human chr17 - 42963556 42963556 42963556 GATAGACGGGTTACAGTAGTACAGCAGAGAGCATATTTATCAGTGCTGTGATGAGGACTAGGTAC GATAGACGGGTTACAGTAGTACAGCAGAGAGCGTATTTATCAGTGCTGTGATGAGGACTAGGTAC T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42963554..42963664 26863196 MeRIP-seq:(Medium) rs987681601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13012883 RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_184514,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 109020 RMVar_ID_109020 Human_SNP_ID_624772848 m1A Human chr17 - 42964234 42964234 42964234 GGCTTATTCTCTCATTCCTCTCTGTTCAGTTCACCACCACCGTGGTCTCCTGCTGTCCCGCGGAG GGCTTATTCTCTCATTCCTCTCTGTTCAGTTCGCCACCACCGTGGTCTCCTGCTGTCCCGCGGAG T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42964073..42964431;chr17:42964095..42964421 26863196 MeRIP-seq:(Medium) rs780005682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1821730,Human_Splice_Rec_1821774,Human_Splice_Rec_1821786,Human_Splice_Rec_1821796,Human_Splice_Rec_1821808,Human_Splice_Rec_1821824,Human_Splice_Rec_1821834,Human_Splice_Rec_1821842,Human_Splice_Rec_1821856,Human_Splice_Rec_1821890,Human_Splice_Rec_1821920,Human_Splice_Rec_1821952,Human_Splice_Rec_1821994,Human_Splice_Rec_1822008 RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_184514,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 109021 RMVar_ID_109021 Human_SNP_ID_624772849 m1A Human chr17 - 42964234 42964234 42964234 GGCTTATTCTCTCATTCCTCTCTGTTCAGTTCACCACCACCGTGGTCTCCTGCTGTCCCGCGGAG GGCTTATTCTCTCATTCCTCTCTGTTCAGTTCCCCACCACCGTGGTCTCCTGCTGTCCCGCGGAG T G AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42964073..42964431;chr17:42964095..42964421 26863196 MeRIP-seq:(Medium) rs780005682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1821730,Human_Splice_Rec_1821774,Human_Splice_Rec_1821786,Human_Splice_Rec_1821796,Human_Splice_Rec_1821808,Human_Splice_Rec_1821824,Human_Splice_Rec_1821834,Human_Splice_Rec_1821842,Human_Splice_Rec_1821856,Human_Splice_Rec_1821890,Human_Splice_Rec_1821920,Human_Splice_Rec_1821952,Human_Splice_Rec_1821994,Human_Splice_Rec_1822008 RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_184514,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 109022 RMVar_ID_109022 Human_SNP_ID_624778187 m1A Human chr17 + 42980650 42980650 42980650 GGCGGCTGTTGGGCCAAAGGCGAAAGACGAAGAGGAGGAGGAAGAGGAGCCGCTGCCACCGTGCG GGCGGCTGTTGGGCCAAAGGCGAAAGACGAAGGGGAGGAGGAAGAGGAGCCGCTGCCACCGTGCG A G RUNDC1 Ensembl:ENSG00000198863 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:42980599..42980773 26863196 MeRIP-seq:(Medium) rs1348131839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4429035,Human_RBP_ID_18419612,Human_RBP_ID_18991431 RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 109023 RMVar_ID_109023 Human_SNP_ID_624780985 m1A Human chr17 - 42990875 42990875 42990875 CTCGCCGCATCAGGTGCAGCCCCGTCTCCCGGACTTTCTTCACATCCTCTGCCTTTGCTGCTTAG CTCGCCGCATCAGGTGCAGCCCCGTCTCCCGGGCTTTCTTCACATCCTCTGCCTTTGCTGCTTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42990845..42990912 26863196 MeRIP-seq:(Medium) rs553638883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27452671 109024 RMVar_ID_109024 Human_SNP_ID_624783170 m1A Human chr17 - 42998729 42998729 42998729 AACTTGCCCATTTCTGCAGAGAGCAAGGAGAAAGGGCCACTTAAAAATCCGTAAAGCCAAAGATG AACTTGCCCATTTCTGCAGAGAGCAAGGAGAACGGGCCACTTAAAAATCCGTAAAGCCAAAGATG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:42998726..42998987;chr17:42998726..42998800 26863196 MeRIP-seq:(Medium) rs1166196080 Functional Loss SNV dbSNP153 33..33 33 - - - 109025 RMVar_ID_109025 Human_SNP_ID_624783536 m1A Human chr17 + 42999997 42999997 42999997 CAGCCATGCTCTGGTGGCTGGAATTGACCGCTACCCCCGCAAAGTGACAGCTGCCATGGGCAAGA CAGCCATGCTCTGGTGGCTGGAATTGACCGCTGCCCCCGCAAAGTGACAGCTGCCATGGGCAAGA A G RPL27 Ensembl:ENSG00000131469 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42999888..43000152 26863196 MeRIP-seq:(Medium) rs1384721873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47832,Human_RBP_ID_236142,Human_RBP_ID_490140,Human_RBP_ID_902124,Human_RBP_ID_1008303,Human_RBP_ID_1534477,Human_RBP_ID_1858772,Human_RBP_ID_3523885,Human_RBP_ID_4429123,Human_RBP_ID_5497074,Human_RBP_ID_8453144,Human_RBP_ID_9072129,Human_RBP_ID_9326661,Human_RBP_ID_13013456,Human_RBP_ID_17654211,Human_RBP_ID_18698468,Human_RBP_ID_22057195,Human_RBP_ID_22214486,Human_RBP_ID_22445521,Human_RBP_ID_22804727,Human_RBP_ID_22960892,Human_RBP_ID_23727332,Human_RBP_ID_26451322,Human_RBP_ID_26813677,Human_RBP_ID_26961867,Human_RBP_ID_27254595 Human_Splice_Rec_1822080,Human_Splice_Rec_1822094,Human_Splice_Rec_1822106,Human_Splice_Rec_1822114 RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_345640,RMVar_hsa_circ_184521,RMVar_hsa_circ_94719,RMVar_hsa_circ_184522,RMVar_hsa_circ_184523,RMVar_hsa_circ_184524 109026 RMVar_ID_109026 Human_SNP_ID_624784468 m1A Human chr17 + 43002800 43002800 43002800 TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTAGTGAATGGTGGAGTATGGTTTCACTATTTCCA TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTCGTGAATGGTGGAGTATGGTTTCACTATTTCCA A C RPL27 Ensembl:ENSG00000131469 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11871636 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_15226,GWAS_ID_15227,GWAS_ID_15228,GWAS_ID_15229 RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_184521,RMVar_hsa_circ_184524,RMVar_hsa_circ_107591,RMVar_hsa_circ_184525 109027 RMVar_ID_109027 Human_SNP_ID_624784469 m1A Human chr17 + 43002800 43002800 43002800 TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTAGTGAATGGTGGAGTATGGTTTCACTATTTCCA TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTTGTGAATGGTGGAGTATGGTTTCACTATTTCCA A T RPL27 Ensembl:ENSG00000131469 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11871636 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15226,GWAS_ID_15227,GWAS_ID_15228,GWAS_ID_15229 RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_184521,RMVar_hsa_circ_184524,RMVar_hsa_circ_107591,RMVar_hsa_circ_184525 109028 RMVar_ID_109028 Human_SNP_ID_624785743 m1A Human chr17 - 43006910 43006910 43006910 TCGGGTCTGTTTGGCAAGAGCTGAGGCTTCAGAGCTGGGCACAGTGGCAGAATTCACAGCAACTG TCGGGTCTGTTTGGCAAGAGCTGAGGCTTCAGGGCTGGGCACAGTGGCAGAATTCACAGCAACTG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43006798..43007021 26863196 MeRIP-seq:(Medium) rs377626634 Functional Loss SNV dbSNP153 33..33 33 - - - 109029 RMVar_ID_109029 Human_SNP_ID_624788425 m1A Human chr17 + 43015796 43015796 43015796 TGGCACAAAAGCAGCACAGCAGGCCCGGGGAAAGGGTGGGGGCAGGAAGCAGCCGGCCTCCCTCT TGGCACAAAAGCAGCACAGCAGGCCCGGGGAATGGGTGGGGGCAGGAAGCAGCCGGCCTCCCTCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:43015451..43015975 32194978 MeRIP-seq:(Medium) rs1192684784 Functional Loss SNV dbSNP153 33..33 33 - - - 109030 RMVar_ID_109030 Human_SNP_ID_624789130 m1A Human chr17 + 43018160 43018160 43018160 TTGCTGGCCGAGGCCGTTCCGAACACTGTCACATTCTCCACTGTACGGCACAGCTGCACGGCAGC TTGCTGGCCGAGGCCGTTCCGAACACTGTCACGTTCTCCACTGTACGGCACAGCTGCACGGCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43018010..43018162 26863196 MeRIP-seq:(Medium) rs1567746548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13013991 109031 RMVar_ID_109031 Human_SNP_ID_624790556 m1A Human chr17 + 43022272 43022272 43022272 TCGCTCGCTGCCTCGGTTTTCGGAGGCGGCGAAGAGGCGTCTTCCCCGGTCGCTGCCTCGGCTAC TCGCTCGCTGCCTCGGTTTTCGGAGGCGGCGATGAGGCGTCTTCCCCGGTCGCTGCCTCGGCTAC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43022112..43022400 26863196 MeRIP-seq:(Medium) rs1210859640 Functional Loss SNV dbSNP153 33..33 33 - - - 109032 RMVar_ID_109032 Human_SNP_ID_624821720 m1A Human chr17 - 43124548 43124548 43124548 AACAGATGCTGCCGGCAGGGATGTGCTTGAGGAGGATCCAGAGATGAGAGCAGGTCACTGGGAAA AACAGATGCTGCCGGCAGGGATGTGCTTGAGGGGGATCCAGAGATGAGAGCAGGTCACTGGGAAA T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43124526..43124726 26863196 MeRIP-seq:(Medium) rs191197821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237469,Human_RBP_ID_5088308,Human_RBP_ID_6596931,Human_RBP_ID_13015442 109033 RMVar_ID_109033 Human_SNP_ID_624825702 m1A Human chr17 - 43138767 43138767 43138767 AGAGCCTGCACGCCTGCTGCTACAGGGGAGGAAAGGATGACTTCTACCTCCTTTCCACATTCCAA AGAGCCTGCACGCCTGCTGCTACAGGGGAGGACAGGATGACTTCTACCTCCTTTCCACATTCCAA T G BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43138716..43138795 26863196 MeRIP-seq:(Medium) rs765401534 Functional Loss SNV dbSNP153 33..33 33 - - - 109034 RMVar_ID_109034 Human_SNP_ID_624832158 m1A Human chr17 - 43166191 43166188 43166192 AGAGAGAGAGGAAGAGACAGGAAGAGACAGACAGAGAGTCAAGGATAGAGAGAGAGAGAGAGAGA AGAGAGAGAGGAAGAGACAGGAAGAGACAGA____GAGTCAAGGATAGAGAGAGAGAGAGAGAGA CTCTG C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43166029..43166289 26863196 MeRIP-seq:(Medium) rs1315641969 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_819024,Human_RBP_ID_5248339,Human_RBP_ID_25286422 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 109035 RMVar_ID_109035 Human_SNP_ID_624832824 m1A Human chr17 + 43168960 43168960 43168960 GCCTCCCTGCCCCTAGCCTTTCCCAGCGACCCACTCTCATCTCAGGATCCCCCTCAAGCACATCC GCCTCCCTGCCCCTAGCCTTTCCCAGCGACCCGCTCTCATCTCAGGATCCCCCTCAAGCACATCC A G lnc-LINC00854-1-001 RNACentral:URS00009AE32C lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:43168953..43169082 26863196 MeRIP-seq:(Medium) rs1251233066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1286547 109036 RMVar_ID_109036 Human_SNP_ID_624832955 m1A Human chr17 - 43169536 43169536 43169536 AGGATCAGGTTGGGGGCACAGTGTGTCCGAGGAGGAATCCTCCTGATAGGAACTGGAATGTGCCT AGGATCAGGTTGGGGGCACAGTGTGTCCGAGGGGGAATCCTCCTGATAGGAACTGGAATGTGCCT T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43169493..43169833 26863196 MeRIP-seq:(Medium) rs1286624806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_901563,Human_RBP_ID_1066604,Human_RBP_ID_1286548 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 109037 RMVar_ID_109037 Human_SNP_ID_624832988 m1A Human chr17 - 43169654 43169654 43169654 TCCGAAGCTAGGCAGATGGGTATTCTTATGCGAGGGGCGGGGGCGGAACCTGAGAGGCATAAGGC TCCGAAGCTAGGCAGATGGGTATTCTTATGCGGGGGGCGGGGGCGGAACCTGAGAGGCATAAGGC T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43169532..43169796 26863196 MeRIP-seq:(Medium) rs1403859149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5582811,Human_RBP_ID_8193740,Human_RBP_ID_26782305 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 109038 RMVar_ID_109038 Human_SNP_ID_624837247 m1A Human chr17 - 43186435 43186435 43186435 AGACTGGGCCATACCCTTCATACCTGCACTGCAGGATCCTCTGGGGTCTTCATGTCTGATCCCAA AGACTGGGCCATACCCTTCATACCTGCACTGCGGGATCCTCTGGGGTCTTCATGTCTGATCCCAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:43177977..43186435 32194978 MeRIP-seq:(Medium) rs748562422 Functional Loss SNV dbSNP153 33..33 33 - - - 109039 RMVar_ID_109039 Human_SNP_ID_624841601 m1A Human chr17 + 43203752 43203752 43203752 GGGGGCTTTGTCTGTTGCTGCCTCTGCATACAAGGCCCTGTTTGCTGGGCCACCAGTCACTGCAC GGGGGCTTTGTCTGTTGCTGCCTCTGCATACAGGGCCCTGTTTGCTGGGCCACCAGTCACTGCAC A G NBR1 Ensembl:ENSG00000188554 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:43201746..43209607 32194978 MeRIP-seq:(Medium) rs1257719149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766636 Human_Splice_Rec_1823018,Human_Splice_Rec_1823019,Human_Splice_Rec_1823096,Human_Splice_Rec_1823097,Human_Splice_Rec_1823138,Human_Splice_Rec_1823139 Human_miRNA_ID_2574631,Human_miRNA_ID_2883264,Human_miRNA_ID_3012547 RMVar_hsa_circ_2746,RMVar_hsa_circ_328568,RMVar_hsa_circ_279289,RMVar_hsa_circ_184574,RMVar_hsa_circ_284170 109040 RMVar_ID_109040 Human_SNP_ID_624842679 m1A Human chr17 + 43208179 43208179 43208179 GAATTTGAGAGTAGAAGTATGCCACACTTTCAAATAGACAGGCTACAACAGGCAGAAGCTAGGAT GAATTTGAGAGTAGAAGTATGCCACACTTTCAGATAGACAGGCTACAACAGGCAGAAGCTAGGAT A G NBR1 Ensembl:ENSG00000188554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43208149..43208241 26863196 MeRIP-seq:(Medium) rs1219498295 Functional Loss SNV dbSNP153 33..33 33 - - - 109041 RMVar_ID_109041 Human_SNP_ID_624843088 m1A Human chr17 + 43209941 43209941 43209941 TTCTGAAGATCAGACAGCAGCCCTGATGGCCCATCTCTTTGAAATGGGATTCTGTGACAGGCAGC TTCTGAAGATCAGACAGCAGCCCTGATGGCCCCTCTCTTTGAAATGGGATTCTGTGACAGGCAGC A C NBR1 Ensembl:ENSG00000188554 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9378294,Human_RBP_ID_22499543 Human_Splice_Rec_1823020,Human_Splice_Rec_1823058,Human_Splice_Rec_1823098 109042 RMVar_ID_109042 Human_SNP_ID_624843089 m1A Human chr17 + 43209941 43209941 43209941 TTCTGAAGATCAGACAGCAGCCCTGATGGCCCATCTCTTTGAAATGGGATTCTGTGACAGGCAGC TTCTGAAGATCAGACAGCAGCCCTGATGGCCCGTCTCTTTGAAATGGGATTCTGTGACAGGCAGC A G NBR1 Ensembl:ENSG00000188554 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8482 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_9378294,Human_RBP_ID_22499543 Human_Splice_Rec_1823020,Human_Splice_Rec_1823058,Human_Splice_Rec_1823098 109043 RMVar_ID_109043 Human_SNP_ID_624845535 m1A Human chr17 - 43219871 43219871 43219871 ACAGCAGTCTCCTTCCTTCCCCTCGTTCCCCCAGCCAGCTAGTTACCAAGTTCTGTCACCACTTC ACAGCAGTCTCCTTCCTTCCCCTCGTTCCCCCGGCCAGCTAGTTACCAAGTTCTGTCACCACTTC T C CCDC200 Ensembl:ENSG00000236383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43219821..43219951 26863196 MeRIP-seq:(Medium) rs1046829376 Functional Loss SNV dbSNP153 33..33 33 - - - 109044 RMVar_ID_109044 Human_SNP_ID_624845542 m1A Human chr17 + 43219890 43219890 43219890 GTAACTAGCTGGCTGGGGGAACGAGGGGAAGGAAGGAGACTGCTGTCTCCAAGCTGAGGTCAGGG GTAACTAGCTGGCTGGGGGAACGAGGGGAAGGCAGGAGACTGCTGTCTCCAAGCTGAGGTCAGGG A C TMEM106A Ensembl:ENSG00000184988 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43219839..43219943 26863196 MeRIP-seq:(Medium) rs568330101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768696 Clinvar_Rec_707,Clinvar_Rec_708,Clinvar_Rec_709 109045 RMVar_ID_109045 Human_SNP_ID_624845543 m1A Human chr17 + 43219890 43219890 43219890 GTAACTAGCTGGCTGGGGGAACGAGGGGAAGGAAGGAGACTGCTGTCTCCAAGCTGAGGTCAGGG GTAACTAGCTGGCTGGGGGAACGAGGGGAAGGGAGGAGACTGCTGTCTCCAAGCTGAGGTCAGGG A G TMEM106A Ensembl:ENSG00000184988 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43219839..43219943 26863196 MeRIP-seq:(Medium) rs568330101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768696 Clinvar_Rec_707,Clinvar_Rec_708,Clinvar_Rec_709 109046 RMVar_ID_109046 Human_SNP_ID_624856427 m1A Human chr17 - 43315997 43315993 43315997 AAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGAAAA AAAACCCCCTCAACACAGCATTCTCAGAAACA____GAAAGAACGCACACACTAAGCTAGGAAAA CTTTT C lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43315967..43316042 26863196 MeRIP-seq:(Medium) rs946520570 Functional Loss DEL dbSNP153 33..36 33 - - - 109047 RMVar_ID_109047 Human_SNP_ID_624856429 m1A Human chr17 - 43315998 43315995 43315999 AAAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGAAA AAAAACCCCCTCAACACAGCATTCTCAGAAA____AAGAAAGAACGCACACACTAAGCTAGGAAA TTTTG T lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43315948..43316146 26863196 MeRIP-seq:(Medium) rs1411029423 Functional Loss DEL dbSNP153 32..35 33 - - - 109048 RMVar_ID_109048 Human_SNP_ID_624856432 m1A Human chr17 - 43315997 43315997 43315997 AAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGAAAA AAAACCCCCTCAACACAGCATTCTCAGAAACATAAAGAAAGAACGCACACACTAAGCTAGGAAAA T A lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43315967..43316042 26863196 MeRIP-seq:(Medium) rs906064963 Functional Loss SNV dbSNP153 33..33 33 - - - 109049 RMVar_ID_109049 Human_SNP_ID_624856433 m1A Human chr17 - 43315997 43315997 43315997 AAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGAAAA AAAACCCCCTCAACACAGCATTCTCAGAAACAGAAAGAAAGAACGCACACACTAAGCTAGGAAAA T C lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43315967..43316042 26863196 MeRIP-seq:(Medium) rs906064963 Functional Loss SNV dbSNP153 33..33 33 - - - 109050 RMVar_ID_109050 Human_SNP_ID_624856436 m1A Human chr17 - 43316000 43316000 43316000 CCAAAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGA CCAAAAACCCCCTCAACACAGCATTCTCAGAAGCAAAAAGAAAGAACGCACACACTAAGCTAGGA T C lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43315950..43316110 26863196 MeRIP-seq:(Medium) rs1000360980 Functional Loss SNV dbSNP153 33..33 33 - - - 109051 RMVar_ID_109051 Human_SNP_ID_624856437 m1A Human chr17 - 43316000 43316000 43316000 CCAAAAACCCCCTCAACACAGCATTCTCAGAAACAAAAAGAAAGAACGCACACACTAAGCTAGGA CCAAAAACCCCCTCAACACAGCATTCTCAGAACCAAAAAGAAAGAACGCACACACTAAGCTAGGA T G lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43315950..43316110 26863196 MeRIP-seq:(Medium) rs1000360980 Functional Loss SNV dbSNP153 33..33 33 - - - 109052 RMVar_ID_109052 Human_SNP_ID_624871321 m1A Human chr17 + 43361201 43361201 43361201 TAACAACGGTCCCAACTGATGCAAATGGCCCAATGCAAACACGTTGACAATCTCCCGTTAGCGAC TAACAACGGTCCCAACTGATGCAAATGGCCCACTGCAAACACGTTGACAATCTCCCGTTAGCGAC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:43361151..43361350 26863196 MeRIP-seq:(Medium) rs986774359 Functional Loss SNV dbSNP153 33..33 33 - - - 109053 RMVar_ID_109053 Human_SNP_ID_624871322 m1A Human chr17 + 43361201 43361201 43361201 TAACAACGGTCCCAACTGATGCAAATGGCCCAATGCAAACACGTTGACAATCTCCCGTTAGCGAC TAACAACGGTCCCAACTGATGCAAATGGCCCAGTGCAAACACGTTGACAATCTCCCGTTAGCGAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:43361151..43361350 26863196 MeRIP-seq:(Medium) rs986774359 Functional Loss SNV dbSNP153 33..33 33 - - - 109054 RMVar_ID_109054 Human_SNP_ID_624871323 m1A Human chr17 + 43361201 43361201 43361201 TAACAACGGTCCCAACTGATGCAAATGGCCCAATGCAAACACGTTGACAATCTCCCGTTAGCGAC TAACAACGGTCCCAACTGATGCAAATGGCCCATTGCAAACACGTTGACAATCTCCCGTTAGCGAC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:43361151..43361350 26863196 MeRIP-seq:(Medium) rs986774359 Functional Loss SNV dbSNP153 33..33 33 - - - 109055 RMVar_ID_109055 Human_SNP_ID_624871349 m1A Human chr17 - 43361221 43361221 43361221 GGCGCTTAGCGTCTGTTACTGTCGCTAACGGGAGATTGTCAACGTGTTTGCATTGGGCCATTTGC GGCGCTTAGCGTCTGTTACTGTCGCTAACGGGGGATTGTCAACGTGTTTGCATTGGGCCATTTGC T C AC109326.1,LINC00910 Ensembl:ENSG00000279602,Ensembl:ENSG00000188825 Other,lincRNA exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:43361176..43361250 26863196 MeRIP-seq:(Medium) rs528978375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17127235,Human_RBP_ID_18419618 109056 RMVar_ID_109056 Human_SNP_ID_624871492 m1A Human chr17 - 43361300 43361300 43361300 GGCTTGTGGTGTTGCTGGCCCTTGATCGCTGGAAGGATTCCGAGGTGTAGTTTTCGAAGCGGGAG GGCTTGTGGTGTTGCTGGCCCTTGATCGCTGGGAGGATTCCGAGGTGTAGTTTTCGAAGCGGGAG T C AC109326.1,LINC00910 Ensembl:ENSG00000279602,Ensembl:ENSG00000188825 Other,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43361207..43361361 26863196 MeRIP-seq:(Medium) rs186605424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549379,Human_RBP_ID_5098539,Human_RBP_ID_5582415,Human_RBP_ID_8453378,Human_RBP_ID_18419618 109057 RMVar_ID_109057 Human_SNP_ID_624871493 m1A Human chr17 - 43361300 43361300 43361300 GGCTTGTGGTGTTGCTGGCCCTTGATCGCTGGAAGGATTCCGAGGTGTAGTTTTCGAAGCGGGAG GGCTTGTGGTGTTGCTGGCCCTTGATCGCTGGCAGGATTCCGAGGTGTAGTTTTCGAAGCGGGAG T G AC109326.1,LINC00910 Ensembl:ENSG00000279602,Ensembl:ENSG00000188825 Other,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43361207..43361361 26863196 MeRIP-seq:(Medium) rs186605424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549379,Human_RBP_ID_5098539,Human_RBP_ID_5582415,Human_RBP_ID_8453378,Human_RBP_ID_18419618 109058 RMVar_ID_109058 Human_SNP_ID_624874253 m1A Human chr17 - 43368951 43368951 43368951 GCGTCGGAACTGGTGGTTCCCTCGGCGGTTCCAGGCCCCTCTCCTCCTTCCCGGGCAGAAGCAGC GCGTCGGAACTGGTGGTTCCCTCGGCGGTTCCGGGCCCCTCTCCTCCTTCCCGGGCAGAAGCAGC T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43368914..43369106 26863196 MeRIP-seq:(Medium) rs1453042484 Functional Loss SNV dbSNP153 33..33 33 - - - 109059 RMVar_ID_109059 Human_SNP_ID_624874391 m1A Human chr17 + 43369304 43369302 43369305 CTTGGGCCAGGATGGGGGCAGTGCGGGGGCTGAGGAGTGGCCAGATTCTGGGTGTACTTTGAAAG CTTGGGCCAGGATGGGGGCAGTGCGGGGGCT___GAGTGGCCAGATTCTGGGTGTACTTTGAAAG TGAG T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43369255..43369372 26863196 MeRIP-seq:(Medium) rs1278787590 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_6597453 109060 RMVar_ID_109060 Human_SNP_ID_624874594 m1A Human chr17 + 43370120 43370116 43370120 GAGAAAGAGTGAGAGAGAAAATTATAAAGTAAATGTGGCCATCAAGGGGAGAGAGAGGGAGTGAA GAGAAAGAGTGAGAGAGAAAATTATAAAG____TGTGGCCATCAAGGGGAGAGAGAGGGAGTGAA GTAAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43370011..43370210 26863196 MeRIP-seq:(Medium) rs1469814920 Functional Loss DEL dbSNP153 30..33 33 - - - 109061 RMVar_ID_109061 Human_SNP_ID_624882312 m1A Human chr17 - 43399647 43399646 43399647 GGGAGCACAGCTGGGTTATCTGAACCAAGAAAAGGTCATGGGAGAAAAAGGAGACGTTTAATAAT GGGAGCACAGCTGGGTTATCTGAACCAAGAAA_GGTCATGGGAGAAAAAGGAGACGTTTAATAAT CT C lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43399644..43400068 26863196 MeRIP-seq:(Medium) rs1314565393 Functional Loss DEL dbSNP153 33..33 33 - - - 109062 RMVar_ID_109062 Human_SNP_ID_624882612 m1A Human chr17 - 43400593 43400592 43400594 AAAAATAAGAAACAGGGTCGAGGTAGAGTCACAGTTTACATTTACGTCTCCACAGTCCTGCAGCG AAAAATAAGAAACAGGGTCGAGGTAGAGTCA__GTTTACATTTACGTCTCCACAGTCCTGCAGCG CTG C lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43400543..43400653 26863196 MeRIP-seq:(Medium) rs1175429755 Functional Loss DEL dbSNP153 32..33 33 - - - 109063 RMVar_ID_109063 Human_SNP_ID_624882613 m1A Human chr17 - 43400593 43400593 43400593 AAAAATAAGAAACAGGGTCGAGGTAGAGTCACAGTTTACATTTACGTCTCCACAGTCCTGCAGCG AAAAATAAGAAACAGGGTCGAGGTAGAGTCACCGTTTACATTTACGTCTCCACAGTCCTGCAGCG T G lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43400543..43400653 26863196 MeRIP-seq:(Medium) rs1044751319 Functional Loss SNV dbSNP153 33..33 33 - - - 109064 RMVar_ID_109064 Human_SNP_ID_624903621 m1A Human chr17 + 43484064 43484064 43484064 ATAGCCATGGCTGTGGCTGTAGCCATGGCGGGAGCCTTAATCGGGTCGGAGCCAGGCCCCGCGGA ATAGCCATGGCTGTGGCTGTAGCCATGGCGGGCGCCTTAATCGGGTCGGAGCCAGGCCCCGCGGA A C DHX8 Ensembl:ENSG00000067596 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43484013..43484119 26863196 MeRIP-seq:(Medium) rs765295823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820052,Human_RBP_ID_4465436,Human_RBP_ID_8818264,Human_RBP_ID_9072205,Human_RBP_ID_9376087,Human_RBP_ID_17063146,Human_RBP_ID_22959425 109065 RMVar_ID_109065 Human_SNP_ID_624903630 m1A Human chr17 + 43484085 43484085 43484085 GCCATGGCGGGAGCCTTAATCGGGTCGGAGCCAGGCCCCGCGGAAGAACTTGCCAAACTCGAGTA GCCATGGCGGGAGCCTTAATCGGGTCGGAGCCGGGCCCCGCGGAAGAACTTGCCAAACTCGAGTA A G DHX8 Ensembl:ENSG00000067596 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43484036..43484105 26863196 MeRIP-seq:(Medium) rs879616965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_820052,Human_RBP_ID_897638,Human_RBP_ID_4465437,Human_RBP_ID_5497093,Human_RBP_ID_8453406,Human_RBP_ID_8824716,Human_RBP_ID_9376087,Human_RBP_ID_22959425,Human_RBP_ID_27812746 109066 RMVar_ID_109066 Human_SNP_ID_624906035 m1A Human chr17 - 43492837 43492837 43492837 GGACTCTGACTCCTGCTCCTGGACCGATATCTAGACTTCACTTTATTCCTCTCCCGGGTCCTGGA GGACTCTGACTCCTGCTCCTGGACCGATATCTGGACTTCACTTTATTCCTCTCCCGGGTCCTGGA T C lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43492786..43492916 26863196 MeRIP-seq:(Medium) rs1311825701 Functional Loss SNV dbSNP153 33..33 33 - - - 109067 RMVar_ID_109067 Human_SNP_ID_624906233 m1A Human chr17 - 43493543 43493543 43493543 TGGTCTTGGTCCCAGTGAAGGACAGCACTTTGACTTTGACCCTCTGGCCTTTGCTCACGACATCA TGGTCTTGGTCCCAGTGAAGGACAGCACTTTGCCTTTGACCCTCTGGCCTTTGCTCACGACATCA T G lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43493494..43493582 26863196 MeRIP-seq:(Medium) rs1218859943 Functional Loss SNV dbSNP153 33..33 33 - - - 109068 RMVar_ID_109068 Human_SNP_ID_624906301 m1A Human chr17 + 43493764 43493764 43493764 ATCTTGTCGGGGAGACCAATGAGGAGACCTCAATGCGGAATCCTGATAGACCCACTCACTTGTCC ATCTTGTCGGGGAGACCAATGAGGAGACCTCAGTGCGGAATCCTGATAGACCCACTCACTTGTCC A G DHX8 Ensembl:ENSG00000067596 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:43493714..43498951 32194978 MeRIP-seq:(Medium) rs1239171144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8818279,Human_RBP_ID_9378305,Human_RBP_ID_18698756 Human_Splice_Rec_1823492,Human_Splice_Rec_1823540,Human_Splice_Rec_1823584,Human_Splice_Rec_1823626 RMVar_hsa_circ_366911,RMVar_hsa_circ_368031,RMVar_hsa_circ_306789,RMVar_hsa_circ_55471,RMVar_hsa_circ_117603,RMVar_hsa_circ_55297,RMVar_hsa_circ_64137,RMVar_hsa_circ_30379,RMVar_hsa_circ_13334,RMVar_hsa_circ_184581,RMVar_hsa_circ_78396,RMVar_hsa_circ_107014,RMVar_hsa_circ_184582,RMVar_hsa_circ_57136,RMVar_hsa_circ_30393,RMVar_hsa_circ_184583,RMVar_hsa_circ_344766,RMVar_hsa_circ_184584 109069 RMVar_ID_109069 Human_SNP_ID_624916204 m1A Human chr17 - 43533332 43533331 43533332 TCCTTCTCAACTCCAGTGCCTATGACCCCCCCAGACAAATCGCCATCAAGTCCCCTGCCCCTGGT TCCTTCTCAACTCCAGTGCCTATGACCCCCCC_GACAAATCGCCATCAAGTCCCCTGCCCCTGGT CT C ETV4 Ensembl:ENSG00000175832 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43533260..43533380 26863196 MeRIP-seq:(Medium) rs779099876 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9327311,Human_RBP_ID_17080280,Human_RBP_ID_18943242,Human_RBP_ID_26812424 Human_Splice_Rec_1823676,Human_Splice_Rec_1823698,Human_Splice_Rec_1823722,Human_Splice_Rec_1823744,Human_Splice_Rec_1823788,Human_Splice_Rec_1823818,Human_Splice_Rec_1823830 109070 RMVar_ID_109070 Human_SNP_ID_624947672 m1A Human chr17 - 43657079 43657067 43657080 GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAAAAGAAAGAAAGAAGGAAGGAAGGAAAGAAAGAAA GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAA_____________GGAAGGAAGGAAAGAAAGAAA CTTCTTTCTTTCTT C MEOX1 Ensembl:ENSG00000005102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43657071..43657143 26863196 MeRIP-seq:(Medium) rs1326731070 Functional Loss DEL dbSNP153 32..44 33 - - - 109071 RMVar_ID_109071 Human_SNP_ID_624947675 m1A Human chr17 - 43657079 43657074 43657079 GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAAAAGAAAGAAAGAAGGAAGGAAGGAAAGAAAGAAA GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAAA_____GAAAGAAGGAAGGAAGGAAAGAAAGAAA CTTTCT C MEOX1 Ensembl:ENSG00000005102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43657071..43657143 26863196 MeRIP-seq:(Medium) rs1485931175 Functional Loss DEL dbSNP153 33..37 33 - - - 109072 RMVar_ID_109072 Human_SNP_ID_624947683 m1A Human chr17 - 43657079 43657078 43657079 GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAAAAGAAAGAAAGAAGGAAGGAAGGAAAGAAAGAAA GAAAAAGAGAGAAAGAAAAAGAAAGAAAGAAA_GAAAGAAAGAAGGAAGGAAGGAAAGAAAGAAA CT C MEOX1 Ensembl:ENSG00000005102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43657071..43657143 26863196 MeRIP-seq:(Medium) rs528807400 Functional Loss DEL dbSNP153 33..33 33 - - - 109073 RMVar_ID_109073 Human_SNP_ID_624985168 m1A Human chr17 - 43817841 43817841 43817841 TCCCTGGAGAGGAGCTTGTATATTTGGAGTCCATAGATGATGCTGGGGGGTATGTTAACAGCTTT TCCCTGGAGAGGAGCTTGTATATTTGGAGTCCGTAGATGATGCTGGGGGGTATGTTAACAGCTTT T C MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43817839..43818029 26863196 MeRIP-seq:(Medium) rs372461903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5362837,Human_RBP_ID_19085269 RMVar_hsa_circ_1397,RMVar_hsa_circ_25821,RMVar_hsa_circ_99276,RMVar_hsa_circ_184611,RMVar_hsa_circ_348447,RMVar_hsa_circ_27266,RMVar_hsa_circ_184615,RMVar_hsa_circ_311655,RMVar_hsa_circ_296486,RMVar_hsa_circ_184614,RMVar_hsa_circ_29099,RMVar_hsa_circ_340435,RMVar_hsa_circ_297972,RMVar_hsa_circ_184617 109074 RMVar_ID_109074 Human_SNP_ID_624989029 m1A Human chr17 + 43832959 43832959 43832959 GGGCGGGCGCGGGAAGAGGGAGGCGGGGGCCGAGGGGCGGGGTTGAGACTCCCGCGGTGGGCTCG GGGCGGGCGCGGGAAGAGGGAGGCGGGGGCCGCGGGGCGGGGTTGAGACTCCCGCGGTGGGCTCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:43832904..43833031 26863196 MeRIP-seq:(Medium) rs1343280241 Functional Loss SNV dbSNP153 33..33 33 - - - 109075 RMVar_ID_109075 Human_SNP_ID_624989049 m1A Human chr17 + 43833025 43833025 43833025 TGGGCCGCGAGGCTGTCCGGGAGCACGGGAGGAGGGTCTCGGCCCGGCCTCCCGCCCCTCCCGCC TGGGCCGCGAGGCTGTCCGGGAGCACGGGAGGGGGGTCTCGGCCCGGCCTCCCGCCCCTCCCGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43833023..43833107 26863196 MeRIP-seq:(Medium) rs1018962965 Functional Loss SNV dbSNP153 33..33 33 - - - 109076 RMVar_ID_109076 Human_SNP_ID_624989053 m1A Human chr17 - 43833042 43833042 43833042 AGGGAGCTGGGCGCCGCGGCGGGAGGGGCGGGAGGCCGGGCCGAGACCCTCCTCCCGTGCTCCCG AGGGAGCTGGGCGCCGCGGCGGGAGGGGCGGGGGGCCGGGCCGAGACCCTCCTCCCGTGCTCCCG T C MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43833040..43833126 26863196 MeRIP-seq:(Medium) rs1341990009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19082835,Human_RBP_ID_26782318 109077 RMVar_ID_109077 Human_SNP_ID_625002434 m1A Human chr17 - 43883339 43883339 43883339 CTGCTTCCACCCCCAGGCCCATGAGAGGCTGGAGGAGACGAAGCTGGAGGCCGTGAGAGACAACA CTGCTTCCACCCCCAGGCCCATGAGAGGCTGGGGGAGACGAAGCTGGAGGCCGTGAGAGACAACA T C MPP2 Ensembl:ENSG00000108852 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43883256..43883392 26863196 MeRIP-seq:(Medium) rs1327622758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1824124,Human_Splice_Rec_1824148,Human_Splice_Rec_1824170,Human_Splice_Rec_1824196,Human_Splice_Rec_1824240,Human_Splice_Rec_1824266,Human_Splice_Rec_1824288,Human_Splice_Rec_1824310,Human_Splice_Rec_1824334,Human_Splice_Rec_1824356,Human_Splice_Rec_1824364,Human_Splice_Rec_1824374,Human_Splice_Rec_1824382,Human_Splice_Rec_1824388,Human_Splice_Rec_1824396,Human_Splice_Rec_1824404,Human_Splice_Rec_1824414,Human_Splice_Rec_1824422,Human_Splice_Rec_1824432 109078 RMVar_ID_109078 Human_SNP_ID_625006018 m1A Human chr17 - 43898325 43898325 43898325 TTGGGATCCCTCCCCAGTGCCACGGGGGCTGCAGAGCTGGACCTGATCTTCCTTCGAGGCATTAT TTGGGATCCCTCCCCAGTGCCACGGGGGCTGCGGAGCTGGACCTGATCTTCCTTCGAGGCATTAT T C MPP2 Ensembl:ENSG00000108852 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43898248..43898451 26863196 MeRIP-seq:(Medium) rs950081821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1824122,Human_Splice_Rec_1824123,Human_Splice_Rec_1824146,Human_Splice_Rec_1824147,Human_Splice_Rec_1824168,Human_Splice_Rec_1824169,Human_Splice_Rec_1824194,Human_Splice_Rec_1824195,Human_Splice_Rec_1824218,Human_Splice_Rec_1824238,Human_Splice_Rec_1824239,Human_Splice_Rec_1824262,Human_Splice_Rec_1824263,Human_Splice_Rec_1824308,Human_Splice_Rec_1824309,Human_Splice_Rec_1824332,Human_Splice_Rec_1824333,Human_Splice_Rec_1824354,Human_Splice_Rec_1824355,Human_Splice_Rec_1824362,Human_Splice_Rec_1824363,Human_Splice_Rec_1824372,Human_Splice_Rec_1824373,Human_Splice_Rec_1824380,Human_Splice_Rec_1824381,Human_Splice_Rec_1824386,Human_Splice_Rec_1824387,Human_Splice_Rec_1824394,Human_Splice_Rec_1824395,Human_Splice_Rec_1824402,Human_Splice_Rec_1824403,Human_Splice_Rec_1824412,Human_Splice_Rec_1824413,Human_Splice_Rec_1824420,Human_Splice_Rec_1824421,Human_Splice_Rec_1824430,Human_Splice_Rec_1824431,Human_Splice_Rec_1824438 109079 RMVar_ID_109079 Human_SNP_ID_625006637 m1A Human chr17 + 43900581 43900581 43900581 CCATGGCGGCCCCCAGACCCGGGGACTCCCGGAGCGTCCTACACGCCGCCGTCTACCGCCTCCCC CCATGGCGGCCCCCAGACCCGGGGACTCCCGGCGCGTCCTACACGCCGCCGTCTACCGCCTCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:43898291..43900602;chr17:43898304..43900602 26863196 MeRIP-seq:(Medium) rs1390342001 Functional Loss SNV dbSNP153 33..33 33 - - - 109080 RMVar_ID_109080 Human_SNP_ID_625006646 m1A Human chr17 + 43900589 43900589 43900589 GCCCCCAGACCCGGGGACTCCCGGAGCGTCCTACACGCCGCCGTCTACCGCCTCCCCAGCCAAAG GCCCCCAGACCCGGGGACTCCCGGAGCGTCCTGCACGCCGCCGTCTACCGCCTCCCCAGCCAAAG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:43900486..43900604 26863196 MeRIP-seq:(Medium) rs1380307840 Functional Loss SNV dbSNP153 33..33 33 - - - 109081 RMVar_ID_109081 Human_SNP_ID_625015897 m1A Human chr17 - 43938591 43938591 43938591 GCTTTTGATGGGGAGGTGTCCGTGGCGTTCGCAGTTTTCTTGTGGTTTTTAGATTTCTTCGGGCT GCTTTTGATGGGGAGGTGTCCGTGGCGTTCGCCGTTTTCTTGTGGTTTTTAGATTTCTTCGGGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:43938517..43938633 26863196 MeRIP-seq:(Medium) rs1490350517 Functional Loss SNV dbSNP153 33..33 33 - - - 109082 RMVar_ID_109082 Human_SNP_ID_625035214 m1A Human chr17 - 44013074 44013074 44013074 TGGCCAGCGGTGCTGGGGAGCTGTACCGCCGGAAACCTCGCAGCCGCTCCCTGCAGTCCACCGGC TGGCCAGCGGTGCTGGGGAGCTGTACCGCCGGTAACCTCGCAGCCGCTCCCTGCAGTCCACCGGC T A TMEM101 Ensembl:ENSG00000091947 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44013026..44013100 32194978 MeRIP-seq:(Medium) rs773473755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22443711,Human_RBP_ID_22760808 Human_Splice_Rec_1824526,Human_Splice_Rec_1824527,Human_Splice_Rec_1824534,Human_Splice_Rec_1824535,Human_Splice_Rec_1824540,Human_Splice_Rec_1824548,Human_Splice_Rec_1824554,Human_Splice_Rec_1824560 RMVar_hsa_circ_120198,RMVar_hsa_circ_184622 109083 RMVar_ID_109083 Human_SNP_ID_625039697 m1A Human chr17 + 44029591 44029591 44029591 CAAACTTCTTCCTCTCCTATTGTTTGCCACCTACCTAGAAGGCATCCATCGTTCCTCTCTGTCCC CAAACTTCTTCCTCTCCTATTGTTTGCCACCTGCCTAGAAGGCATCCATCGTTCCTCTCTGTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44029545..44029747 26863196 MeRIP-seq:(Medium) rs1198169595 Functional Loss SNV dbSNP153 33..33 33 - - - 109084 RMVar_ID_109084 Human_SNP_ID_625050273 m1A Human chr17 + 44066599 44066599 44066599 CTCGCCCGGAGGAGCCGCCATCTTGGGAGTGCAGCCGCGGCCGGCGGCGGCGGCGGCAGCAGCGG CTCGCCCGGAGGAGCCGCCATCTTGGGAGTGCGGCCGCGGCCGGCGGCGGCGGCGGCAGCAGCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:44066553..44066622;chr17:44066529..44066614 26863196 MeRIP-seq:(Medium) rs1215548100 Functional Loss SNV dbSNP153 33..33 33 - - - 109085 RMVar_ID_109085 Human_SNP_ID_625051514 m1A Human chr17 - 44070814 44070814 44070814 CCCGCCAGCGGTCACCACCAAGCCCCGCCCCCAGCAGTCCCCCGCTCCTGCAAGACCGGCCTCCA CCCGCCAGCGGTCACCACCAAGCCCCGCCCCCGGCAGTCCCCCGCTCCTGCAAGACCGGCCTCCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44070764..44070850 26863196 MeRIP-seq:(Medium) rs149756661 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_710 109086 RMVar_ID_109086 Human_SNP_ID_625051515 m1A Human chr17 - 44070814 44070814 44070814 CCCGCCAGCGGTCACCACCAAGCCCCGCCCCCAGCAGTCCCCCGCTCCTGCAAGACCGGCCTCCA CCCGCCAGCGGTCACCACCAAGCCCCGCCCCCCGCAGTCCCCCGCTCCTGCAAGACCGGCCTCCA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44070764..44070850 26863196 MeRIP-seq:(Medium) rs149756661 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_710 109087 RMVar_ID_109087 Human_SNP_ID_625052774 m1A Human chr17 - 44075010 44075006 44075010 TGAAGATTCGCGACAAGCCAACCGCCAAAAGGAAGGTGCAATAAGCCAGGCTAGGCATCACCCTT TGAAGATTCGCGACAAGCCAACCGCCAAAAGG____TGCAATAAGCCAGGCTAGGCATCACCCTT ACCTT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44074681..44075077 32194978 MeRIP-seq:(Medium) rs780038679 Functional Loss DEL dbSNP153 33..36 33 - - - 109088 RMVar_ID_109088 Human_SNP_ID_625053167 m1A Human chr17 + 44075995 44075995 44075995 CCATGCCTAGTCCTGGCCCTCGTGCCCTGGGCAGTGCACATGTTCAGTGCCCAGGAAGCACCGCC CCATGCCTAGTCCTGGCCCTCGTGCCCTGGGCGGTGCACATGTTCAGTGCCCAGGAAGCACCGCC A G G6PC3 Ensembl:ENSG00000141349 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:44075951..44076000 26863196 MeRIP-seq:(Medium) rs1246530023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490656,Human_RBP_ID_8453626,Human_RBP_ID_17263994,Human_RBP_ID_17378748,Human_RBP_ID_17494943,Human_RBP_ID_17654225,Human_RBP_ID_18698922,Human_RBP_ID_20172291 Human_miRNA_ID_254226,Human_miRNA_ID_461528,Human_miRNA_ID_927662 109089 RMVar_ID_109089 Human_SNP_ID_625058569 m1A Human chr17 - 44093391 44093391 44093391 GGAGCTGGAGCAGCAGCGGCAGCGGGAGCAGCAGCGGCAGGAAGAGCTGGAGAAGCAGCGGCTGG GGAGCTGGAGCAGCAGCGGCAGCGGGAGCAGCGGCGGCAGGAAGAGCTGGAGAAGCAGCGGCTGG T C HDAC5 Ensembl:ENSG00000108840 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44093342..44093453 26863196 MeRIP-seq:(Medium) rs752275402 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_18991496 Human_Splice_Rec_1824664,Human_Splice_Rec_1824665,Human_Splice_Rec_1824716,Human_Splice_Rec_1824717,Human_Splice_Rec_1824764,Human_Splice_Rec_1824765,Human_Splice_Rec_1824865 RMVar_hsa_circ_23679,RMVar_hsa_circ_115913,RMVar_hsa_circ_184627,RMVar_hsa_circ_46539,RMVar_hsa_circ_45933,RMVar_hsa_circ_367146,RMVar_hsa_circ_53295,RMVar_hsa_circ_33070 109090 RMVar_ID_109090 Human_SNP_ID_625058575 m1A Human chr17 - 44093397 44093397 44093397 GCAGCAGGAGCTGGAGCAGCAGCGGCAGCGGGAGCAGCAGCGGCAGGAAGAGCTGGAGAAGCAGC GCAGCAGGAGCTGGAGCAGCAGCGGCAGCGGGGGCAGCAGCGGCAGGAAGAGCTGGAGAAGCAGC T C HDAC5 Ensembl:ENSG00000108840 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44093351..44093451 26863196 MeRIP-seq:(Medium) rs1372728385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18991496 Human_Splice_Rec_1824664,Human_Splice_Rec_1824665,Human_Splice_Rec_1824716,Human_Splice_Rec_1824717,Human_Splice_Rec_1824764,Human_Splice_Rec_1824765,Human_Splice_Rec_1824865 RMVar_hsa_circ_23679,RMVar_hsa_circ_115913,RMVar_hsa_circ_184627,RMVar_hsa_circ_46539,RMVar_hsa_circ_45933,RMVar_hsa_circ_367146,RMVar_hsa_circ_53295,RMVar_hsa_circ_33070 109091 RMVar_ID_109091 Human_SNP_ID_625065159 m1A Human chr17 + 44117696 44117696 44117696 ATCCTTCGGGGCGAGGCAGTCAGGCACTCAGAACGGCATCCCTGGGGAGAGATGGAGCAGGGTTA ATCCTTCGGGGCGAGGCAGTCAGGCACTCAGAGCGGCATCCCTGGGGAGAGATGGAGCAGGGTTA A G AC023855.2 Ensembl:ENSG00000267638 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44117558..44117746 26863196 MeRIP-seq:(Medium) rs1422571949 Functional Loss SNV dbSNP153 33..33 33 - - - 109092 RMVar_ID_109092 Human_SNP_ID_625066634 m1A Human chr17 + 44123425 44123425 44123425 GCGCGGCGCGCGCGCTGGGAGCCCGCGGACAGAGACAGCAGGAGGAGGGGGCGCCGCCTCGCGTC GCGCGGCGCGCGCGCTGGGAGCCCGCGGACAGGGACAGCAGGAGGAGGGGGCGCCGCCTCGCGTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:44123392..44123518 26863196 MeRIP-seq:(Medium) rs1347334959 Functional Loss SNV dbSNP153 33..33 33 - - - 109093 RMVar_ID_109093 Human_SNP_ID_625066649 m1A Human chr17 - 44123482 44123482 44123482 AGCCGCAGCGGGTGAGCGCGCCGCCCCGGCCCAGATCCCATCTTCCCCGGACCCCGGGACGCGAG AGCCGCAGCGGGTGAGCGCGCCGCCCCGGCCCGGATCCCATCTTCCCCGGACCCCGGGACGCGAG T C HDAC5 Ensembl:ENSG00000108840 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44123480..44123600 26863410 MeRIP-seq:(Medium) rs1241477548 Functional Loss SNV dbSNP153 33..33 33 - - - 109094 RMVar_ID_109094 Human_SNP_ID_625066868 m1A Human chr17 + 44123872 44123872 44123872 GGCCGAGACGGGGTGGAAGGGAAGGGATCGGAACCCAGCGAGCAGGAGTGGAAGGATCGCTGCAG GGCCGAGACGGGGTGGAAGGGAAGGGATCGGAGCCCAGCGAGCAGGAGTGGAAGGATCGCTGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44123865..44123968 26863196 MeRIP-seq:(Medium) rs1404484133 Functional Loss SNV dbSNP153 33..33 33 - - - 109095 RMVar_ID_109095 Human_SNP_ID_625073645 m1A Human chr17 + 44148179 44148179 44148179 GAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCC GAAGAGTGACAGTGACAGAAGTGCTCAGAGAGCCAGCAAGACCTCAGTCCTCAGCCTTACACCCC A C HROB Ensembl:ENSG00000125319 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs227584 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_miRNA_ID_1265074,Human_miRNA_ID_2611674 GWAS_ID_15230,GWAS_ID_15231,GWAS_ID_15232,GWAS_ID_15233,GWAS_ID_15234,GWAS_ID_15235,GWAS_ID_15236,GWAS_ID_15237,GWAS_ID_15238,GWAS_ID_15239,GWAS_ID_15240,GWAS_ID_15241,GWAS_ID_15242,GWAS_ID_15243,GWAS_ID_15244,GWAS_ID_15245,GWAS_ID_15246,GWAS_ID_15247,GWAS_ID_15248,GWAS_ID_15249,GWAS_ID_15250,GWAS_ID_15251,GWAS_ID_15252 RMVar_hsa_circ_184642,RMVar_hsa_circ_8262,RMVar_hsa_circ_312362,RMVar_hsa_circ_286468 109096 RMVar_ID_109096 Human_SNP_ID_625084920 m1A Human chr17 + 44187307 44187307 44187307 GGACAACTGGTCTTATCACGGAGGCTGGGGCCAGGCAGCCCTTCGGTTCGGGTGGGCCCATGGAC GGACAACTGGTCTTATCACGGAGGCTGGGGCCGGGCAGCCCTTCGGTTCGGGTGGGCCCATGGAC A G TMUB2 Ensembl:ENSG00000168591 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44187058..44187409 26863196 MeRIP-seq:(Medium) rs1336478212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4464583,Human_RBP_ID_17893239 Human_Splice_Rec_1825049 RMVar_hsa_circ_120224,RMVar_hsa_circ_184653 109097 RMVar_ID_109097 Human_SNP_ID_625086075 m1A Human chr17 + 44190627 44190627 44190627 ACCGACAACTGTGTGATTCACTGCCACCGCTCACCCCCAGGGTCAGCTGTTCCAGGCCCCTCAGC ACCGACAACTGTGTGATTCACTGCCACCGCTCGCCCCCAGGGTCAGCTGTTCCAGGCCCCTCAGC A G TMUB2 Ensembl:ENSG00000168591 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44190579..44190692 26863196 MeRIP-seq:(Medium) rs768588135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1008417,Human_RBP_ID_22061381,Human_RBP_ID_22443721 RMVar_hsa_circ_92489,RMVar_hsa_circ_85310,RMVar_hsa_circ_120224,RMVar_hsa_circ_184653,RMVar_hsa_circ_88250,RMVar_hsa_circ_184654,RMVar_hsa_circ_184655,RMVar_hsa_circ_102516,RMVar_hsa_circ_184657,RMVar_hsa_circ_184658 109098 RMVar_ID_109098 Human_SNP_ID_625086537 m1A Human chr17 - 44191905 44191905 44191905 CTGTCCTGTGGTCTTGAGATTTTTATTTTTGCATATGTAATCCATTCTGTACAGGTAGCTAACTT CTGTCCTGTGGTCTTGAGATTTTTATTTTTGCGTATGTAATCCATTCTGTACAGGTAGCTAACTT T C ATXN7L3 Ensembl:ENSG00000087152 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44191854..44192053 32194978 MeRIP-seq:(Medium) rs1021559573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490725,Human_RBP_ID_1182133,Human_RBP_ID_1534787,Human_RBP_ID_1859212,Human_RBP_ID_2508072,Human_RBP_ID_3524485,Human_RBP_ID_5114704,Human_RBP_ID_5144200,Human_RBP_ID_8191127,Human_RBP_ID_13022170,Human_RBP_ID_18164226,Human_RBP_ID_21890134,Human_RBP_ID_21975571,Human_RBP_ID_24417327,Human_RBP_ID_24479291,Human_RBP_ID_26459308,Human_RBP_ID_26642583 RMVar_hsa_circ_83849,RMVar_hsa_circ_105487,RMVar_hsa_circ_122629,RMVar_hsa_circ_120424,RMVar_hsa_circ_104459,RMVar_hsa_circ_184659,RMVar_hsa_circ_184661,RMVar_hsa_circ_184662,RMVar_hsa_circ_184663,RMVar_hsa_circ_184660 109099 RMVar_ID_109099 Human_SNP_ID_625086678 m1A Human chr17 + 44192199 44192199 44192199 GAGTGGGGAGCTCCTAGCCCCTGTTCAACTACATGGTAGGGGGGGCACTCTCTCCCCAGAAGGAA GAGTGGGGAGCTCCTAGCCCCTGTTCAACTACGTGGTAGGGGGGGCACTCTCTCCCCAGAAGGAA A G lnc-TMUB2-2 RNACentral:URS00008B5D0F lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44192151..44192498 32194978 MeRIP-seq:(Medium) rs1428404896 Functional Loss SNV dbSNP153 33..33 33 - - - 109100 RMVar_ID_109100 Human_SNP_ID_625087016 m1A Human chr17 - 44193281 44193277 44193281 TCCCAACTGCTGCTTCCACCCCCTTCACCTTGACTGGCTTCAGTTCCTCTCAGCGCTCCTGCCTC TCCCAACTGCTGCTTCCACCCCCTTCACCTTG____GCTTCAGTTCCTCTCAGCGCTCCTGCCTC CCAGT C ATXN7L3 Ensembl:ENSG00000087152 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44193243..44193366 26863196 MeRIP-seq:(Medium) rs549323202 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6598625,Human_RBP_ID_18190857,Human_RBP_ID_18941752 Human_miRNA_ID_2697841 RMVar_hsa_circ_83849,RMVar_hsa_circ_105487,RMVar_hsa_circ_122629,RMVar_hsa_circ_120424,RMVar_hsa_circ_104459,RMVar_hsa_circ_184659,RMVar_hsa_circ_184661,RMVar_hsa_circ_184662,RMVar_hsa_circ_184663,RMVar_hsa_circ_184660 109101 RMVar_ID_109101 Human_SNP_ID_625089265 m1A Human chr17 + 44199450 44199443 44199450 AGCCCCGCCTTGGGCCCCGCCCCCCGCCCCCCACAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC AGCCCCGCCTTGGGCCCCGCCCCCCG_______CAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC GCCCCCCA G AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44199439..44199575 26863410 MeRIP-seq:(Medium) rs1401111178 Functional Loss DEL dbSNP153 27..33 33 - - - 109102 RMVar_ID_109102 Human_SNP_ID_625089273 m1A Human chr17 + 44199450 44199450 44199450 AGCCCCGCCTTGGGCCCCGCCCCCCGCCCCCCACAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC AGCCCCGCCTTGGGCCCCGCCCCCCGCCCCCCCCAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC A C AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44199439..44199575 26863410 MeRIP-seq:(Medium) rs1248806121 Functional Loss SNV dbSNP153 33..33 33 - - - 109103 RMVar_ID_109103 Human_SNP_ID_625089274 m1A Human chr17 + 44199450 44199450 44199450 AGCCCCGCCTTGGGCCCCGCCCCCCGCCCCCCACAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC AGCCCCGCCTTGGGCCCCGCCCCCCGCCCCCCGCAGGCCCCTCCCCCGTCCCCGTCCCCGTCTCC A G AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44199439..44199575 26863410 MeRIP-seq:(Medium) rs1248806121 Functional Loss SNV dbSNP153 33..33 33 - - - 109104 RMVar_ID_109104 Human_SNP_ID_625089341 m1A Human chr17 - 44199591 44199591 44199591 CCTGGGCCCCGGGGAGAGGCGAGGACGGACCGACGGACATGGGGCTCCGGAGCAGCCGCCGCCGT CCTGGGCCCCGGGGAGAGGCGAGGACGGACCGCCGGACATGGGGCTCCGGAGCAGCCGCCGCCGT T G ATXN7L3 Ensembl:ENSG00000087152 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:44199471..44199964;chr17:44199473..44200113;chr17:44199470..44200113 26863196 MeRIP-seq:(Medium) rs1251190173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541707,Human_RBP_ID_3950704,Human_RBP_ID_4466482,Human_RBP_ID_5143566,Human_RBP_ID_8192033,Human_RBP_ID_8824721,Human_RBP_ID_8941824,Human_RBP_ID_9327315,Human_RBP_ID_9422892,Human_RBP_ID_18419974,Human_RBP_ID_18941755,Human_RBP_ID_26457743 Human_Splice_Rec_1825151 109105 RMVar_ID_109105 Human_SNP_ID_625089402 m1A Human chr17 - 44199716 44199716 44199716 CTGCGCGCGGGCGGGGTGAGGTGAGGAGGAGGAGGCGGCGACGGGACAAGAAGGGAGGGGAAGGG CTGCGCGCGGGCGGGGTGAGGTGAGGAGGAGGCGGCGGCGACGGGACAAGAAGGGAGGGGAAGGG T G ATXN7L3 Ensembl:ENSG00000087152 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:44199642..44199763 26863410 MeRIP-seq:(Medium) rs1164783433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3541708,Human_RBP_ID_6598658,Human_RBP_ID_8192033,Human_RBP_ID_8825584,Human_RBP_ID_9326674,Human_RBP_ID_17067950,Human_RBP_ID_21974376 109106 RMVar_ID_109106 Human_SNP_ID_625089406 m1A Human chr17 - 44199722 44199722 44199722 CGCGGACTGCGCGCGGGCGGGGTGAGGTGAGGAGGAGGAGGCGGCGACGGGACAAGAAGGGAGGG CGCGGACTGCGCGCGGGCGGGGTGAGGTGAGGCGGAGGAGGCGGCGACGGGACAAGAAGGGAGGG T G ATXN7L3 Ensembl:ENSG00000087152 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr17:44199559..44200113;chr17:44199659..44199849 26863196 MeRIP-seq:(Medium) rs1436855051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6598658,Human_RBP_ID_8192033,Human_RBP_ID_8825584,Human_RBP_ID_17067950,Human_RBP_ID_21974376 109107 RMVar_ID_109107 Human_SNP_ID_625089456 m1A Human chr17 - 44199843 44199841 44199843 CGCTCCATCCATCCATCCTCCGGTCGCGGCACACGCGCGCGCGCTCCGGGCTCGCGCCGCACCCC CGCTCCATCCATCCATCCTCCGGTCGCGGCAC__GCGCGCGCGCTCCGGGCTCGCGCCGCACCCC CGT C ATXN7L3 Ensembl:ENSG00000087152 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:44199653..44199862 26863196 MeRIP-seq:(Medium) rs1192341882 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5441486,Human_RBP_ID_5497119 109108 RMVar_ID_109108 Human_SNP_ID_625091692 m1A Human chr17 - 44207247 44207247 44207247 CCTCCTCAGGGGACTCCTCAGACTCTGACTCCAACTGAGGCTCAGCCCCACCCCAGGGCAGCCAG CCTCCTCAGGGGACTCCTCAGACTCTGACTCCGACTGAGGCTCAGCCCCACCCCAGGGCAGCCAG T C UBTF Ensembl:ENSG00000108312 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44207201..44207250 26863196 MeRIP-seq:(Medium) rs1182678863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_50375,Human_RBP_ID_8818442,Human_RBP_ID_9376119,Human_RBP_ID_13022300,Human_RBP_ID_26330768,Human_RBP_ID_27452977,Human_RBP_ID_27812750 109109 RMVar_ID_109109 Human_SNP_ID_625091827 m1A Human chr17 + 44207526 44207526 44207526 GAGGAGTCGCCGCCATCTTCAGAGGAGTCCCCATTCTCATCATCTTCCTCTTCTTCATCCTCGTC GAGGAGTCGCCGCCATCTTCAGAGGAGTCCCCGTTCTCATCATCTTCCTCTTCTTCATCCTCGTC A G AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44207191..44207600 26863196 MeRIP-seq:(Medium) rs1346811615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549315 109110 RMVar_ID_109110 Human_SNP_ID_625092512 m1A Human chr17 - 44209386 44209386 44209386 GCACTACAAAAAGCTGGCCGAGGAGCAGCAAAAGCAGTACAAGGTGCACCTGGACCTCTGGGTTA GCACTACAAAAAGCTGGCCGAGGAGCAGCAAAGGCAGTACAAGGTGCACCTGGACCTCTGGGTTA T C UBTF Ensembl:ENSG00000108312 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44209376..44209400 26863196 MeRIP-seq:(Medium) rs1392411800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17904921,Human_RBP_ID_27812752 Human_Splice_Rec_1825249,Human_Splice_Rec_1825289,Human_Splice_Rec_1825329,Human_Splice_Rec_1825367,Human_Splice_Rec_1825405,Human_Splice_Rec_1825443,Human_Splice_Rec_1825479,Human_Splice_Rec_1825517,Human_Splice_Rec_1825525 Human_miRNA_ID_2360220,Human_miRNA_ID_2751120 RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 109111 RMVar_ID_109111 Human_SNP_ID_625093035 m1A Human chr17 - 44210760 44210760 44210760 GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCAGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCTGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG T A UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44210755..44210886 26863196 MeRIP-seq:(Medium) rs2526011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19082864,Human_RBP_ID_22061384 RMVar_hsa_circ_4823,RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 109112 RMVar_ID_109112 Human_SNP_ID_625093036 m1A Human chr17 - 44210760 44210760 44210760 GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCAGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCGGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG T C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44210755..44210886 26863196 MeRIP-seq:(Medium) rs2526011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19082864,Human_RBP_ID_22061384 RMVar_hsa_circ_4823,RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 109113 RMVar_ID_109113 Human_SNP_ID_625093037 m1A Human chr17 - 44210760 44210760 44210760 GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCAGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCCGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG T G UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44210755..44210886 26863196 MeRIP-seq:(Medium) rs2526011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19082864,Human_RBP_ID_22061384 RMVar_hsa_circ_4823,RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 109114 RMVar_ID_109114 Human_SNP_ID_625094123 m1A Human chr17 - 44213977 44213975 44213978 GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAAAAGGGGGTGATGAAGGGAAGGGAAGCCAAGTGGT GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAA___GGGGTGATGAAGGGAAGGGAAGCCAAGTGGT CCTT C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44213771..44214124 26863196 MeRIP-seq:(Medium) rs956845481 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_768168,Human_RBP_ID_18941757,Human_RBP_ID_23728538 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119 109115 RMVar_ID_109115 Human_SNP_ID_625094126 m1A Human chr17 - 44213977 44213976 44213977 GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAAAAGGGGGTGATGAAGGGAAGGGAAGCCAAGTGGT GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAAA_GGGGGTGATGAAGGGAAGGGAAGCCAAGTGGT CT C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44213771..44214124 26863196 MeRIP-seq:(Medium) rs773376073 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_768168,Human_RBP_ID_18941757,Human_RBP_ID_23728538 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119 109116 RMVar_ID_109116 Human_SNP_ID_625094127 m1A Human chr17 - 44213977 44213977 44213977 GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAAAAGGGGGTGATGAAGGGAAGGGAAGCCAAGTGGT GAGGGAGTGAGGTGAGAGTGGGGAGGCTAAAAGGGGGGTGATGAAGGGAAGGGAAGCCAAGTGGT T C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44213771..44214124 26863196 MeRIP-seq:(Medium) rs1330566740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768168,Human_RBP_ID_18941757,Human_RBP_ID_23728538 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119 109117 RMVar_ID_109117 Human_SNP_ID_625094148 m1A Human chr17 - 44214070 44214069 44214071 GAGCCAAGAGAGAAGGTCGATGAGGAAGAGAAAGAGACACATTGGAAAGGAGGAACAAGAAGGAG GAGCCAAGAGAGAAGGTCGATGAGGAAGAGA__GAGACACATTGGAAAGGAGGAACAAGAAGGAG CTT C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:44213640..44214135;chr17:44213744..44214148 26863196 MeRIP-seq:(Medium) rs1237781075 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13022351 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119 109118 RMVar_ID_109118 Human_SNP_ID_625094149 m1A Human chr17 - 44214070 44214070 44214070 GAGCCAAGAGAGAAGGTCGATGAGGAAGAGAAAGAGACACATTGGAAAGGAGGAACAAGAAGGAG GAGCCAAGAGAGAAGGTCGATGAGGAAGAGAAGGAGACACATTGGAAAGGAGGAACAAGAAGGAG T C UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:44213640..44214135;chr17:44213744..44214148 26863196 MeRIP-seq:(Medium) rs957539790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13022351 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119 109119 RMVar_ID_109119 Human_SNP_ID_625094539 m1A Human chr17 + 44215540 44215540 44215540 TGTGGCTGCCCAGGACCTATTCTGCTGTGCTGACTCACCCTCATCCCTGATGCCAGGTTTCTCCA TGTGGCTGCCCAGGACCTATTCTGCTGTGCTGCCTCACCCTCATCCCTGATGCCAGGTTTCTCCA A C AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44215491..44215634 26863196 MeRIP-seq:(Medium) rs984319205 Functional Loss SNV dbSNP153 33..33 33 - - - 109120 RMVar_ID_109120 Human_SNP_ID_625095268 m1A Human chr17 - 44218250 44218250 44218250 GACCCCGGGTTGCCCGGCCAGCACGACCGAGGAGGTGGCTGGACAGCTGGAGGATGAACGGAGAA GACCCCGGGTTGCCCGGCCAGCACGACCGAGGTGGTGGCTGGACAGCTGGAGGATGAACGGAGAA T A UBTF Ensembl:ENSG00000108312 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44218201..44218306 26863196 MeRIP-seq:(Medium) rs577524223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1534831,Human_RBP_ID_3524518,Human_RBP_ID_4464593,Human_RBP_ID_6598758,Human_RBP_ID_8818491,Human_RBP_ID_9289170,Human_RBP_ID_9376148,Human_RBP_ID_13022408,Human_RBP_ID_17893323,Human_RBP_ID_26331900 Human_Splice_Rec_1825220,Human_Splice_Rec_1825221,Human_Splice_Rec_1825258,Human_Splice_Rec_1825259,Human_Splice_Rec_1825298,Human_Splice_Rec_1825299,Human_Splice_Rec_1825338,Human_Splice_Rec_1825339,Human_Splice_Rec_1825376,Human_Splice_Rec_1825377,Human_Splice_Rec_1825414,Human_Splice_Rec_1825415,Human_Splice_Rec_1825451,Human_Splice_Rec_1825487,Human_Splice_Rec_1825549,Human_Splice_Rec_1825555 RMVar_hsa_circ_4823,RMVar_hsa_circ_48784,RMVar_hsa_circ_60125,RMVar_hsa_circ_348139,RMVar_hsa_circ_9119,RMVar_hsa_circ_365500,RMVar_hsa_circ_58950 109121 RMVar_ID_109121 Human_SNP_ID_625095538 m1A Human chr17 + 44218822 44218796 44218822 ACGCAGCGCAGCCGCCGCCAGCCCCGGAGCGGAGCGGCCGCACCGCCCCCGGGGACCGGATCCGG ACGCAGC__________________________GCGGCCGCACCGCCCCCGGGGACCGGATCCGG CGCAGCCGCCGCCAGCCCCGGAGCGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44218819..44219117 26863196 MeRIP-seq:(Medium) rs1386602478 Functional Loss DEL dbSNP153 8..33 33 - - - 109122 RMVar_ID_109122 Human_SNP_ID_625095546 m1A Human chr17 + 44218817 44218813 44218818 CCCGGACGCAGCGCAGCCGCCGCCAGCCCCGGAGCGGAGCGGCCGCACCGCCCCCGGGGACCGGA CCCGGACGCAGCGCAGCCGCCGCCAGCCC_____CGGAGCGGCCGCACCGCCCCCGGGGACCGGA CCGGAG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:44218801..44219050 26863196 MeRIP-seq:(Medium) rs902355785 Functional Loss DEL dbSNP153 30..34 33 - - - 109123 RMVar_ID_109123 Human_SNP_ID_625095727 m1A Human chr17 + 44219224 44219224 44219224 GCCGGGGAGAACTGCGCCTGCCGGCTCCGAGAAGCGCGGGCTCCTCCGCCAGCGGCCGGGGCTCG GCCGGGGAGAACTGCGCCTGCCGGCTCCGAGACGCGCGGGCTCCTCCGCCAGCGGCCGGGGCTCG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44219218..44219467 26863410 MeRIP-seq:(Medium) rs1193662698 Functional Loss SNV dbSNP153 33..33 33 - - - 109124 RMVar_ID_109124 Human_SNP_ID_625095950 m1A Human chr17 + 44219757 44219724 44219757 GCCTCAGCTCGCACACCCCCCGCCGCCGCCGCAGCCTCAGCCGCCGGAGCGGGGAGGAGGAGGGA _________________________________GCCTCAGCCGCCGGAGCGGGGAGGAGGAGGGA GGCCTCAGCTCGCACACCCCCCGCCGCCGCCGCA G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:44219706..44219983 26863196 MeRIP-seq:(Medium) rs1429123593 Functional Loss DEL dbSNP153 1..33 33 - - - 109125 RMVar_ID_109125 Human_SNP_ID_625096494 m1A Human chr17 + 44220713 44220713 44220713 CCGCCGCCACTCGTAGCAACCCCTCTCCCCCGAAATCCGCGGCTCCCGGGCTCACTTACCGAGCG CCGCCGCCACTCGTAGCAACCCCTCTCCCCCGGAATCCGCGGCTCCCGGGCTCACTTACCGAGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44220710..44220856 26863196 MeRIP-seq:(Medium) rs995059464 Functional Loss SNV dbSNP153 33..33 33 - - - 109126 RMVar_ID_109126 Human_SNP_ID_625096495 m1A Human chr17 + 44220713 44220713 44220713 CCGCCGCCACTCGTAGCAACCCCTCTCCCCCGAAATCCGCGGCTCCCGGGCTCACTTACCGAGCG CCGCCGCCACTCGTAGCAACCCCTCTCCCCCGTAATCCGCGGCTCCCGGGCTCACTTACCGAGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44220710..44220856 26863196 MeRIP-seq:(Medium) rs995059464 Functional Loss SNV dbSNP153 33..33 33 - - - 109127 RMVar_ID_109127 Human_SNP_ID_625123706 m1A Human chr17 + 44319651 44319651 44319651 CACCAGGCAGAAGTTCATCATCTTTAGACTTAAGGAATTAACAAGGGTCAGGGAGACTACACCAG CACCAGGCAGAAGTTCATCATCTTTAGACTTACGGAATTAACAAGGGTCAGGGAGACTACACCAG A C NONHSAG021924.2,NONHSAG021924.2:2 RNACentral:URS00009C2BE9,RNACentral:URS00008C2D40 lincRNA,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44319626..44319650 26863196 MeRIP-seq:(Medium) rs1254303930 Functional Loss SNV dbSNP153 33..33 33 - - - 109128 RMVar_ID_109128 Human_SNP_ID_625124138 m1A Human chr17 + 44320600 44320600 44320600 AGGCCCCCCGCAGGGAGACCTCCGCTGGCCTCACCTCCAGCCCAGTCCACTCACCGTCCCTGAGA AGGCCCCCCGCAGGGAGACCTCCGCTGGCCTCGCCTCCAGCCCAGTCCACTCACCGTCCCTGAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44320597..44320695 26863196 MeRIP-seq:(Medium) rs762351754 Functional Loss SNV dbSNP153 33..33 33 - - - 109129 RMVar_ID_109129 Human_SNP_ID_625124328 m1A Human chr17 - 44321156 44321156 44321156 AAAGCTGCAGGCTCAGCATGTGTCGTACCGGGAGCTGGGTGCCTGTGTTCGAACTGCAGTGGCTC AAAGCTGCAGGCTCAGCATGTGTCGTACCGGGCGCTGGGTGCCTGTGTTCGAACTGCAGTGGCTC T G SLC25A39 Ensembl:ENSG00000013306 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1392239987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490850,Human_RBP_ID_3524542,Human_RBP_ID_5185262,Human_RBP_ID_17692185,Human_RBP_ID_17904925,Human_RBP_ID_18699082,Human_RBP_ID_23118902,Human_RBP_ID_23728622,Human_RBP_ID_24479303 Human_Splice_Rec_1825786,Human_Splice_Rec_1825787,Human_Splice_Rec_1825805,Human_Splice_Rec_1825826,Human_Splice_Rec_1825827,Human_Splice_Rec_1825848,Human_Splice_Rec_1825849,Human_Splice_Rec_1825862,Human_Splice_Rec_1825863,Human_Splice_Rec_1825871,Human_Splice_Rec_1825896,Human_Splice_Rec_1825897,Human_Splice_Rec_1825910,Human_Splice_Rec_1825911 RMVar_hsa_circ_91296,RMVar_hsa_circ_96273,RMVar_hsa_circ_100815,RMVar_hsa_circ_93105,RMVar_hsa_circ_82693,RMVar_hsa_circ_184678,RMVar_hsa_circ_184680,RMVar_hsa_circ_184681,RMVar_hsa_circ_184679,RMVar_hsa_circ_184677 109130 RMVar_ID_109130 Human_SNP_ID_625124341 m1A Human chr17 - 44321171 44321171 44321171 GGAGCTTATGCGGACAAAGCTGCAGGCTCAGCATGTGTCGTACCGGGAGCTGGGTGCCTGTGTTC GGAGCTTATGCGGACAAAGCTGCAGGCTCAGCGTGTGTCGTACCGGGAGCTGGGTGCCTGTGTTC T C SLC25A39 Ensembl:ENSG00000013306 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44321122..44321251 26863196 MeRIP-seq:(Medium) rs749362656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490850,Human_RBP_ID_3524542,Human_RBP_ID_4473879,Human_RBP_ID_5185262,Human_RBP_ID_13022765,Human_RBP_ID_17904925,Human_RBP_ID_23118902,Human_RBP_ID_23728623,Human_RBP_ID_24479303 Human_Splice_Rec_1825786,Human_Splice_Rec_1825826,Human_Splice_Rec_1825848,Human_Splice_Rec_1825862,Human_Splice_Rec_1825896,Human_Splice_Rec_1825910 Human_miRNA_ID_2954374,Human_miRNA_ID_2954375,Human_miRNA_ID_2958117,Human_miRNA_ID_2958118 RMVar_hsa_circ_91296,RMVar_hsa_circ_96273,RMVar_hsa_circ_100815,RMVar_hsa_circ_93105,RMVar_hsa_circ_82693,RMVar_hsa_circ_184678,RMVar_hsa_circ_184680,RMVar_hsa_circ_184681,RMVar_hsa_circ_184679,RMVar_hsa_circ_184677 109131 RMVar_ID_109131 Human_SNP_ID_625124511 m1A Human chr17 - 44321505 44321505 44321505 CGCCATCTACTTCACTGCCTATGACCAACTGAAGGCCTTCCTGTGTGGTCGAGCCCTGACCTCTG CGCCATCTACTTCACTGCCTATGACCAACTGACGGCCTTCCTGTGTGGTCGAGCCCTGACCTCTG T G SLC25A39 Ensembl:ENSG00000013306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:44321379..44321593;chr17:44321376..44321568 26863196 MeRIP-seq:(Medium) rs755813200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1090633,Human_RBP_ID_18190864,Human_RBP_ID_18991522 Human_Splice_Rec_1825784,Human_Splice_Rec_1825785,Human_Splice_Rec_1825804,Human_Splice_Rec_1825824,Human_Splice_Rec_1825825,Human_Splice_Rec_1825846,Human_Splice_Rec_1825847,Human_Splice_Rec_1825860,Human_Splice_Rec_1825861,Human_Splice_Rec_1825894,Human_Splice_Rec_1825895,Human_Splice_Rec_1825908,Human_Splice_Rec_1825909,Human_Splice_Rec_1825928,Human_Splice_Rec_1825940,Human_Splice_Rec_1825952,Human_Splice_Rec_1825962 Human_miRNA_ID_1966496,Human_miRNA_ID_1966497,Human_miRNA_ID_2361953,Human_miRNA_ID_2361954 RMVar_hsa_circ_91296,RMVar_hsa_circ_96273,RMVar_hsa_circ_100815,RMVar_hsa_circ_93105,RMVar_hsa_circ_82693,RMVar_hsa_circ_184678,RMVar_hsa_circ_184680,RMVar_hsa_circ_184681,RMVar_hsa_circ_184679,RMVar_hsa_circ_184677,RMVar_hsa_circ_184682,RMVar_hsa_circ_77014 109132 RMVar_ID_109132 Human_SNP_ID_625124634 m1A Human chr17 - 44321734 44321734 44321734 ATGCCTTCGTGAAGATCGTGAGGCACGAGGGCACCAGGACCCTCTGGAGCGGCCTCCCCGCCACC ATGCCTTCGTGAAGATCGTGAGGCACGAGGGCCCCAGGACCCTCTGGAGCGGCCTCCCCGCCACC T G SLC25A39 Ensembl:ENSG00000013306 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs998219009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490859,Human_RBP_ID_764316,Human_RBP_ID_1534839,Human_RBP_ID_3952517,Human_RBP_ID_4466495,Human_RBP_ID_18190865,Human_RBP_ID_18991523,Human_RBP_ID_26812436 Human_Splice_Rec_1825782,Human_Splice_Rec_1825783,Human_Splice_Rec_1825802,Human_Splice_Rec_1825803,Human_Splice_Rec_1825822,Human_Splice_Rec_1825823,Human_Splice_Rec_1825844,Human_Splice_Rec_1825845,Human_Splice_Rec_1825858,Human_Splice_Rec_1825859,Human_Splice_Rec_1825892,Human_Splice_Rec_1825893,Human_Splice_Rec_1825906,Human_Splice_Rec_1825907,Human_Splice_Rec_1825926,Human_Splice_Rec_1825927,Human_Splice_Rec_1825938,Human_Splice_Rec_1825939,Human_Splice_Rec_1825950,Human_Splice_Rec_1825951,Human_Splice_Rec_1825960,Human_Splice_Rec_1825961 Human_miRNA_ID_2825861,Human_miRNA_ID_2825862,Human_miRNA_ID_2859834,Human_miRNA_ID_2859835 RMVar_hsa_circ_91296,RMVar_hsa_circ_96273,RMVar_hsa_circ_100815,RMVar_hsa_circ_93105,RMVar_hsa_circ_82693,RMVar_hsa_circ_184678,RMVar_hsa_circ_184680,RMVar_hsa_circ_184681,RMVar_hsa_circ_184679,RMVar_hsa_circ_184677 109133 RMVar_ID_109133 Human_SNP_ID_625124905 m1A Human chr17 + 44322483 44322483 44322483 ACCAGGTGGCACAGCGGGCACCATTTGGGCACAGGTACAGAGGCTCCAGGACACCATTGCAATAC ACCAGGTGGCACAGCGGGCACCATTTGGGCACGGGTACAGAGGCTCCAGGACACCATTGCAATAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44322375..44322584 26863196 MeRIP-seq:(Medium) rs372460117 Functional Loss SNV dbSNP153 33..33 33 - - - 109134 RMVar_ID_109134 Human_SNP_ID_625125258 m1A Human chr17 - 44323361 44323361 44323361 CCTAGGGGTGGGGTCCTGAAAGGAGCCTTCAGACCCGCTTCCTCCCCCAGTGACACCCCTGGACG CCTAGGGGTGGGGTCCTGAAAGGAGCCTTCAGTCCCGCTTCCTCCCCCAGTGACACCCCTGGACG T A SLC25A39 Ensembl:ENSG00000013306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44323355..44323455 26863196 MeRIP-seq:(Medium) rs767779397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3952520,Human_RBP_ID_5361898,Human_RBP_ID_8189678,Human_RBP_ID_22475122,Human_RBP_ID_22543372,Human_RBP_ID_22656411,Human_RBP_ID_26781210 Human_Splice_Rec_1825777,Human_Splice_Rec_1825797,Human_Splice_Rec_1825817,Human_Splice_Rec_1825839,Human_Splice_Rec_1825889,Human_Splice_Rec_1825923,Human_Splice_Rec_1825933,Human_Splice_Rec_1825945,Human_Splice_Rec_1825957,Human_Splice_Rec_1825967,Human_Splice_Rec_1825977,Human_Splice_Rec_1825985,Human_Splice_Rec_1825991 RMVar_hsa_circ_96273,RMVar_hsa_circ_93105,RMVar_hsa_circ_184680,RMVar_hsa_circ_184681,RMVar_hsa_circ_286847,RMVar_hsa_circ_184684 109135 RMVar_ID_109135 Human_SNP_ID_625125671 m1A Human chr17 - 44324340 44324340 44324340 TGGTCACCGGATCTGTTTACACGTCACCCTCGATGCCCGGCCGTCCCTCCACGCCCAGTAACTTG TGGTCACCGGATCTGTTTACACGTCACCCTCGGTGCCCGGCCGTCCCTCCACGCCCAGTAACTTG T C SLC25A39 Ensembl:ENSG00000013306 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8079946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46820 Human_Splice_Rec_1825971 GWAS_ID_15253,GWAS_ID_15254,GWAS_ID_15255,GWAS_ID_15256,GWAS_ID_15257,GWAS_ID_15258,GWAS_ID_15259 RMVar_hsa_circ_93105,RMVar_hsa_circ_184681 109136 RMVar_ID_109136 Human_SNP_ID_625125690 m1A Human chr17 - 44324389 44324389 44324389 AGGGCCGGGCATCCCAGCCCGCAGTCCTGAGGAGGCGACGGGCCCTTCTTGGTCACCGGATCTGT AGGGCCGGGCATCCCAGCCCGCAGTCCTGAGGCGGCGACGGGCCCTTCTTGGTCACCGGATCTGT T G SLC25A39 Ensembl:ENSG00000013306 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:44324376..44324567 26863196 MeRIP-seq:(Medium) rs1011552095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19086305 Human_Splice_Rec_1825971 RMVar_hsa_circ_93105,RMVar_hsa_circ_184681 109137 RMVar_ID_109137 Human_SNP_ID_625125777 m1A Human chr17 - 44324672 44324672 44324672 GGCACTGGGCCGGGGCTGGGGGCGGAGACGGAAGCGGGGGTCTCCGGGCGGCCGTGCGAGCCAGG GGCACTGGGCCGGGGCTGGGGGCGGAGACGGACGCGGGGGTCTCCGGGCGGCCGTGCGAGCCAGG T G SLC25A39 Ensembl:ENSG00000013306 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44324669..44324850 26863410 MeRIP-seq:(Medium) rs575337946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235604,Human_RBP_ID_262305,Human_RBP_ID_819279,Human_RBP_ID_898558,Human_RBP_ID_1066607,Human_RBP_ID_3541715,Human_RBP_ID_3950711,Human_RBP_ID_5186146,Human_RBP_ID_5318422,Human_RBP_ID_5362882,Human_RBP_ID_8232024,Human_RBP_ID_8727059,Human_RBP_ID_9422355,Human_RBP_ID_17126650,Human_RBP_ID_17653852,Human_RBP_ID_18419624,Human_RBP_ID_18459704,Human_RBP_ID_19079301,Human_RBP_ID_21975093,Human_RBP_ID_22357292,Human_RBP_ID_22442995,Human_RBP_ID_22586165,Human_RBP_ID_24552301,Human_RBP_ID_26781415,Human_RBP_ID_27838464 RMVar_hsa_circ_93105,RMVar_hsa_circ_184681 109138 RMVar_ID_109138 Human_SNP_ID_625125789 m1A Human chr17 + 44324709 44324709 44324709 TCTCCGCCCCCAGCCCCGGCCCAGTGCCGCCTACCTGGCTCTAGGCTGGTGCTCGTGCGGCGCGG TCTCCGCCCCCAGCCCCGGCCCAGTGCCGCCTCCCTGGCTCTAGGCTGGTGCTCGTGCGGCGCGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44324701..44324725 26863196 MeRIP-seq:(Medium) rs966273536 Functional Loss SNV dbSNP153 33..33 33 - - - 109139 RMVar_ID_109139 Human_SNP_ID_625132338 m1A Human chr17 - 44349222 44349222 44349222 GCAGGCCACAGGGCAGAACTGACCATCTGGGCACCGCGTTCCAGCCACCAGCCCTGCTGTTAAGG GCAGGCCACAGGGCAGAACTGACCATCTGGGCGCCGCGTTCCAGCCACCAGCCCTGCTGTTAAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44349151..44349327 26863196 MeRIP-seq:(Medium) rs542613543 Functional Loss SNV dbSNP153 33..33 33 - - - 109140 RMVar_ID_109140 Human_SNP_ID_625132549 m1A Human chr17 - 44349709 44349709 44349709 GAAGCAGGATCGCCCGTCTGCACTGCAGTGGAAGCCCCGTGGGCAGCAGTGATGGCCATCCCCGC GAAGCAGGATCGCCCGTCTGCACTGCAGTGGATGCCCCGTGGGCAGCAGTGATGGCCATCCCCGC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44349701..44349725 26863196 MeRIP-seq:(Medium) rs902451602 Functional Loss SNV dbSNP153 33..33 33 - - - 109141 RMVar_ID_109141 Human_SNP_ID_625132550 m1A Human chr17 - 44349709 44349709 44349709 GAAGCAGGATCGCCCGTCTGCACTGCAGTGGAAGCCCCGTGGGCAGCAGTGATGGCCATCCCCGC GAAGCAGGATCGCCCGTCTGCACTGCAGTGGAGGCCCCGTGGGCAGCAGTGATGGCCATCCCCGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44349701..44349725 26863196 MeRIP-seq:(Medium) rs902451602 Functional Loss SNV dbSNP153 33..33 33 - - - 109142 RMVar_ID_109142 Human_SNP_ID_625132738 m1A Human chr17 - 44350287 44350285 44350288 CCAGGAGCCATCGACCATAACACAGCACGTGGAGAAGTCCGGGCATTCGAACTGACTATCAGGGC CCAGGAGCCATCGACCATAACACAGCACGTG___AAGTCCGGGCATTCGAACTGACTATCAGGGC TCTC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44350237..44350356 26863196 MeRIP-seq:(Medium) rs1367342063 Functional Loss DEL dbSNP153 32..34 33 - - - 109143 RMVar_ID_109143 Human_SNP_ID_625132871 m1A Human chr17 + 44350571 44350570 44350572 TGGCAAAGAAGCTCCCTGCCCAGAGGACTAACAGGGCAGGTGAGGAGGTGGGAGAGCATCAGGCC TGGCAAAGAAGCTCCCTGCCCAGAGGACTAAC__GGCAGGTGAGGAGGTGGGAGAGCATCAGGCC CAG C GRN Ensembl:ENSG00000030582 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44350451..44350600 32194978 MeRIP-seq:(Medium) rs1555611136 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22761559,Human_RBP_ID_26812443 Human_Splice_Rec_1826089,Human_Splice_Rec_1826103,Human_Splice_Rec_1826147,Human_Splice_Rec_1826159,Human_Splice_Rec_1826171,Human_Splice_Rec_1826175 Human_miRNA_ID_3091132 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_184690 109144 RMVar_ID_109144 Human_SNP_ID_625132950 m1A Human chr17 + 44350750 44350750 44350750 CGGACGCACGGTCCCGGTGCCCTGATGGTTCTACCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC CGGACGCACGGTCCCGGTGCCCTGATGGTTCTGCCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC A G GRN Ensembl:ENSG00000030582 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44350676..44350800 32194978 MeRIP-seq:(Medium) rs63750683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4431065,Human_RBP_ID_22443731,Human_RBP_ID_22760829,Human_RBP_ID_22804837,Human_RBP_ID_23728636 Human_Splice_Rec_1826090,Human_Splice_Rec_1826091,Human_Splice_Rec_1826104,Human_Splice_Rec_1826105,Human_Splice_Rec_1826148,Human_Splice_Rec_1826149,Human_Splice_Rec_1826160,Human_Splice_Rec_1826161,Human_Splice_Rec_1826172,Human_Splice_Rec_1826173,Human_Splice_Rec_1826176,Human_Splice_Rec_1826177,Human_Splice_Rec_1826187 Human_miRNA_ID_599157,Human_miRNA_ID_1045806,Human_miRNA_ID_2223409,Human_miRNA_ID_2486480,Human_miRNA_ID_3074845 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691 109145 RMVar_ID_109145 Human_SNP_ID_625132951 m1A Human chr17 + 44350750 44350750 44350750 CGGACGCACGGTCCCGGTGCCCTGATGGTTCTACCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC CGGACGCACGGTCCCGGTGCCCTGATGGTTCTTCCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC A T GRN Ensembl:ENSG00000030582 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44350676..44350800 32194978 MeRIP-seq:(Medium) rs63750683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4431065,Human_RBP_ID_22443731,Human_RBP_ID_22760829,Human_RBP_ID_22804837,Human_RBP_ID_23728636 Human_Splice_Rec_1826090,Human_Splice_Rec_1826091,Human_Splice_Rec_1826104,Human_Splice_Rec_1826105,Human_Splice_Rec_1826148,Human_Splice_Rec_1826149,Human_Splice_Rec_1826160,Human_Splice_Rec_1826161,Human_Splice_Rec_1826172,Human_Splice_Rec_1826173,Human_Splice_Rec_1826176,Human_Splice_Rec_1826177,Human_Splice_Rec_1826187 Human_miRNA_ID_599157,Human_miRNA_ID_1045806,Human_miRNA_ID_2223409,Human_miRNA_ID_2486480,Human_miRNA_ID_3074845 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691 109146 RMVar_ID_109146 Human_SNP_ID_625133125 m1A Human chr17 + 44351142 44351138 44351142 TCTCCAAGGAGAACGCTACCACGGACCTCCTCACTAAGCTGCCTGCGCACACAGGTACCAGAGGC TCTCCAAGGAGAACGCTACCACGGACCTC____CTAAGCTGCCTGCGCACACAGGTACCAGAGGC CCTCA C GRN Ensembl:ENSG00000030582 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44351009..44351161 26863196 MeRIP-seq:(Medium) rs63749877 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_1286665,Human_RBP_ID_1368499,Human_RBP_ID_22760831,Human_RBP_ID_26812444 Human_Splice_Rec_1826107,Human_Splice_Rec_1826163,Human_Splice_Rec_1826179 Clinvar_Rec_711 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_106530,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691,RMVar_hsa_circ_265063,RMVar_hsa_circ_184692,RMVar_hsa_circ_46629,RMVar_hsa_circ_268864 109147 RMVar_ID_109147 Human_SNP_ID_625133193 m1A Human chr17 + 44351337 44351333 44351338 GATACCCCTGAGGGTCCCCAGTGCCACTTCTGACCTGTCCTCTCTGCTTCCCTCACAGTGGGGGA GATACCCCTGAGGGTCCCCAGTGCCACTT_____CTGTCCTCTCTGCTTCCCTCACAGTGGGGGA TCTGAC T GRN Ensembl:ENSG00000030582 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44351335..44351458 26863196 MeRIP-seq:(Medium) rs765408713 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_22543373,Human_RBP_ID_22656415 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_106530,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691,RMVar_hsa_circ_265063,RMVar_hsa_circ_184692,RMVar_hsa_circ_268864 109148 RMVar_ID_109148 Human_SNP_ID_625133536 m1A Human chr17 - 44352137 44352137 44352137 TCACAGCCGATGTCTCTGGGGTGGGATAAGGAAGCCCGGCGGGCAGGCATCTTCTCCAGTCCAGC TCACAGCCGATGTCTCTGGGGTGGGATAAGGAGGCCCGGCGGGCAGGCATCTTCTCCAGTCCAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44352001..44352152 26863196 MeRIP-seq:(Medium) rs1449210466 Functional Loss SNV dbSNP153 33..33 33 - - - 109149 RMVar_ID_109149 Human_SNP_ID_625133902 m1A Human chr17 + 44352998 44352998 44352998 GGGTTGTGGCAAAAGCCACATTACAAGCTGCCATCCCCTCCCCGTTTCAGTGGACCCTGTGGCCA GGGTTGTGGCAAAAGCCACATTACAAGCTGCCGTCCCCTCCCCGTTTCAGTGGACCCTGTGGCCA A G GRN Ensembl:ENSG00000030582 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44352976..44353000 32194978 MeRIP-seq:(Medium) rs1412264728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235632,Human_RBP_ID_490893,Human_RBP_ID_3524551,Human_RBP_ID_5114720,Human_RBP_ID_5143570,Human_RBP_ID_8453813,Human_RBP_ID_8947818,Human_RBP_ID_17378752,Human_RBP_ID_17654242,Human_RBP_ID_23728649 Human_miRNA_ID_420735 RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_106530,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691,RMVar_hsa_circ_184692,RMVar_hsa_circ_94458,RMVar_hsa_circ_184694,RMVar_hsa_circ_77417,RMVar_hsa_circ_102094,RMVar_hsa_circ_119130,RMVar_hsa_circ_87932,RMVar_hsa_circ_184695,RMVar_hsa_circ_184696,RMVar_hsa_circ_184697,RMVar_hsa_circ_184698 109150 RMVar_ID_109150 Human_SNP_ID_625134099 m1A Human chr17 + 44353653 44353653 44353653 CCTCTCCGGCCTGGGGCTGGGAGCTACGCGCGAGGGCCCCCGCGGGCCCCCGGGGCGCGCACCCT CCTCTCCGGCCTGGGGCTGGGAGCTACGCGCGGGGGCCCCCGCGGGCCCCCGGGGCGCGCACCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44353613..44354013 32194978 MeRIP-seq:(Medium) rs1348388646 Functional Loss SNV dbSNP153 33..33 33 - - - 109151 RMVar_ID_109151 Human_SNP_ID_625134438 m1A Human chr17 + 44354694 44354694 44354694 GCCCCGCCTGGCCCAGCGACGGCGGCCGCGCCAGCTGGTCCACCGACTGCGACAGCAGGAAGTCG GCCCCGCCTGGCCCAGCGACGGCGGCCGCGCCGGCTGGTCCACCGACTGCGACAGCAGGAAGTCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44354498..44354734 26863410 MeRIP-seq:(Medium) rs897116068 Functional Loss SNV dbSNP153 33..33 33 - - - 109152 RMVar_ID_109152 Human_SNP_ID_625134604 m1A Human chr17 + 44355145 44355145 44355145 CTGGTCTCGTTTGTTACCGTCAGAGGGCCCCGAGAGCTGCAGCTTGCGGTGCTGTTGCCTCGGCT CTGGTCTCGTTTGTTACCGTCAGAGGGCCCCGGGAGCTGCAGCTTGCGGTGCTGTTGCCTCGGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44354561..44358978 32194978 MeRIP-seq:(Medium) rs1249115955 Functional Loss SNV dbSNP153 33..33 33 - - - 109153 RMVar_ID_109153 Human_SNP_ID_625146270 m1A Human chr17 - 44395882 44395882 44395882 CAGGCTCTCAGCCCTAATTAACACACTGACCCAAAGGTGCTTGTGTTGCAGGTCCCATCTCCTTT CAGGCTCTCAGCCCTAATTAACACACTGACCCGAAGGTGCTTGTGTTGCAGGTCCCATCTCCTTT T C GPATCH8 Ensembl:ENSG00000186566 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44395832..44395932 26863196 MeRIP-seq:(Medium) rs1364835554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8191152,Human_RBP_ID_20219696 109154 RMVar_ID_109154 Human_SNP_ID_625146846 m1A Human chr17 - 44397625 44397625 44397625 GCAGCTGCCACTGCACTTCACCTTCACCCACTACTTCACCCCATCTTCTCAGGTCAGGACCTGCA GCAGCTGCCACTGCACTTCACCTTCACCCACTTCTTCACCCCATCTTCTCAGGTCAGGACCTGCA T A GPATCH8 Ensembl:ENSG00000186566 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44397576..44398052 26863196 MeRIP-seq:(Medium) rs757072106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129179,Human_RBP_ID_13023170,Human_RBP_ID_17080056,Human_RBP_ID_17260038,Human_RBP_ID_17375900,Human_RBP_ID_17491565,Human_RBP_ID_17893386,Human_RBP_ID_18530681,Human_RBP_ID_18943278,Human_RBP_ID_22422077,Human_RBP_ID_27453042 109155 RMVar_ID_109155 Human_SNP_ID_625146869 m1A Human chr17 - 44397684 44397684 44397684 TTCACCCTGTCCCACATGCTGCCCTCTACCCCACCCTACTTGCTCCACGGCCTGCTGCAGCAGCT TTCACCCTGTCCCACATGCTGCCCTCTACCCCCCCCTACTTGCTCCACGGCCTGCTGCAGCAGCT T G GPATCH8 Ensembl:ENSG00000186566 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:44397616..44397935 26863196 MeRIP-seq:(Medium) rs993095236 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5129179,Human_RBP_ID_9072306,Human_RBP_ID_17079624,Human_RBP_ID_17264000,Human_RBP_ID_17494949,Human_RBP_ID_18941766 Human_miRNA_ID_42029,Human_miRNA_ID_70747,Human_miRNA_ID_598774,Human_miRNA_ID_1045537 109156 RMVar_ID_109156 Human_SNP_ID_625146888 m1A Human chr17 + 44397744 44397744 44397744 GTGAAAGGTGAAGGGCCCAGGATGGATGGCTGAGGCGGGAATGATGTGGATGGGATGGCTAGCGA GTGAAAGGTGAAGGGCCCAGGATGGATGGCTGGGGCGGGAATGATGTGGATGGGATGGCTAGCGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44397575..44398014 26863196 MeRIP-seq:(Medium) rs887438680 Functional Loss SNV dbSNP153 33..33 33 - - - 109157 RMVar_ID_109157 Human_SNP_ID_625147814 m1A Human chr17 - 44400008 44400008 44400008 GAAGCACAAAAAATCCAGCAAACACAAACGTAAACACAAGGCTGACACAGAAGAGAAAAGCTCTA GAAGCACAAAAAATCCAGCAAACACAAACGTAGACACAAGGCTGACACAGAAGAGAAAAGCTCTA T C GPATCH8 Ensembl:ENSG00000186566 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44399831..44400102 26863196 MeRIP-seq:(Medium) rs1178138498 Functional Loss SNV dbSNP153 33..33 33 - - - 109158 RMVar_ID_109158 Human_SNP_ID_625147817 m1A Human chr17 - 44400013 44400013 44400013 AAAAAGAAGCACAAAAAATCCAGCAAACACAAACGTAAACACAAGGCTGACACAGAAGAGAAAAG AAAAAGAAGCACAAAAAATCCAGCAAACACAAGCGTAAACACAAGGCTGACACAGAAGAGAAAAG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44399772..44400181 26863196 MeRIP-seq:(Medium) rs1393628819 Functional Loss SNV dbSNP153 33..33 33 - - - 109159 RMVar_ID_109159 Human_SNP_ID_625148006 m1A Human chr17 - 44400655 44400655 44400655 CAGCCGAAGGAAACCAGCATGACCGAGCCCTCAGAACCAGGAAGCAAAGCTGAGGCAAAGAAGGC CAGCCGAAGGAAACCAGCATGACCGAGCCCTCGGAACCAGGAAGCAAAGCTGAGGCAAAGAAGGC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44400610..44400757 26863196 MeRIP-seq:(Medium) rs1567934322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9376157,Human_RBP_ID_26331923,Human_RBP_ID_27812762 109160 RMVar_ID_109160 Human_SNP_ID_625173563 m1A Human chr17 - 44503414 44503414 44503414 CCGGGGAGGGGTGGGTGTCGCAGGAGGGAAGGAGCGAACCGGAGAGCGTCGTCCTGAGAGGAGTG CCGGGGAGGGGTGGGTGTCGCAGGAGGGAAGGCGCGAACCGGAGAGCGTCGTCCTGAGAGGAGTG T G GPATCH8 Ensembl:ENSG00000186566 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44503293..44503593 26863196 MeRIP-seq:(Medium) rs1394662690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326687,Human_RBP_ID_9422357,Human_RBP_ID_18419979,Human_RBP_ID_18991531 Human_Splice_Rec_1826427,Human_Splice_Rec_1826463,Human_Splice_Rec_1826479,Human_Splice_Rec_1826491,Human_Splice_Rec_1826517,Human_Splice_Rec_1826529,Human_Splice_Rec_1826539,Human_Splice_Rec_1826543 RMVar_hsa_circ_90707,RMVar_hsa_circ_184712 109161 RMVar_ID_109161 Human_SNP_ID_625181537 m1A Human chr17 - 44533991 44533991 44533991 GGCTGCCACGGAATTTGGAAACTAACATCAGCATAAGGCCTGGATGATTCATTGCTGCAGCGAAG GGCTGCCACGGAATTTGGAAACTAACATCAGCGTAAGGCCTGGATGATTCATTGCTGCAGCGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44533942..44534036 26863196 MeRIP-seq:(Medium) rs1002998253 Functional Loss SNV dbSNP153 33..33 33 - - - 109162 RMVar_ID_109162 Human_SNP_ID_625187051 m1A Human chr17 - 44557392 44557392 44557392 TCAGCTCCCCCTCTCCCCTCCCTTCTGCACCCAGCGACTTCTTTGTGCCTCCTCCAGCCCTCACC TCAGCTCCCCCTCTCCCCTCCCTTCTGCACCCGGCGACTTCTTTGTGCCTCCTCCAGCCCTCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44557287..44557610 26863196 MeRIP-seq:(Medium) rs887954312 Functional Loss SNV dbSNP153 33..33 33 - - - 109163 RMVar_ID_109163 Human_SNP_ID_625187070 m1A Human chr17 + 44557450 44557450 44557450 GAGCTGAGAGGCGAGAGGAGGAGGAAGAGGAGAGAGGGCAGCAGCGCGCGGTGTCTCCGGCTGCT GAGCTGAGAGGCGAGAGGAGGAGGAAGAGGAGCGAGGGCAGCAGCGCGCGGTGTCTCCGGCTGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44557276..44557899 26863196 MeRIP-seq:(Medium) rs1291164826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4431383 109164 RMVar_ID_109164 Human_SNP_ID_625187340 m1A Human chr17 + 44558165 44558165 44558165 ATCTGCGTCGGCCAGAACCACTCCGAGGACGGAGCTCCCGCGCTACTCACCACCGCGCCGCCGCC ATCTGCGTCGGCCAGAACCACTCCGAGGACGGGGCTCCCGCGCTACTCACCACCGCGCCGCCGCC A G FZD2 Ensembl:ENSG00000180340 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44558115..44558341 26863196 MeRIP-seq:(Medium) rs1488529571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27453096 109165 RMVar_ID_109165 Human_SNP_ID_625187426 m1A Human chr17 - 44558414 44558414 44558414 ACCGACCAGGTGAGGATCCAGAGGCGCGCGAAACGCGTCTCCTCCTGTGAGAAGAACATGGAACC ACCGACCAGGTGAGGATCCAGAGGCGCGCGAATCGCGTCTCCTCCTGTGAGAAGAACATGGAACC T A lnc-GPATCH8-2 RNACentral:URS00008C3477 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44558243..44558441 32194978 MeRIP-seq:(Medium) rs1220634584 Functional Loss SNV dbSNP153 33..33 33 - - - 109166 RMVar_ID_109166 Human_SNP_ID_625190308 m1A Human chr17 - 44569078 44569056 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC_______________________CGGAGAAATAG GGGGGGGGGGGGGGGGGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1384672635 Functional Loss DEL dbSNP153 32..54 33 - - - 109167 RMVar_ID_109167 Human_SNP_ID_625190313 m1A Human chr17 - 44569078 44569062 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC_________________CCCCCCCGGAGAAATAG GGGGGGGGGGGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108530 Functional Loss DEL dbSNP153 32..48 33 - - - 109168 RMVar_ID_109168 Human_SNP_ID_625190314 m1A Human chr17 - 44569078 44569064 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC_______________CCCCCCCCCGGAGAAATAG GGGGGGGGGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1393480680 Functional Loss DEL dbSNP153 32..46 33 - - - 109169 RMVar_ID_109169 Human_SNP_ID_625190316 m1A Human chr17 - 44569078 44569065 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC______________CCCCCCCCCCGGAGAAATAG GGGGGGGGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs796116172 Functional Loss DEL dbSNP153 32..45 33 - - - 109170 RMVar_ID_109170 Human_SNP_ID_625190321 m1A Human chr17 - 44569078 44569067 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC____________CCCCCCCCCCCCGGAGAAATAG GGGGGGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs58903526 Functional Loss DEL dbSNP153 32..43 33 - - - 109171 RMVar_ID_109171 Human_SNP_ID_625190324 m1A Human chr17 - 44569078 44569067 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCA___________CCCCCCCCCCCCGGAGAAATAG GGGGGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108551 Functional Loss DEL dbSNP153 33..43 33 - - - 109172 RMVar_ID_109172 Human_SNP_ID_625190329 m1A Human chr17 - 44569078 44569068 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCA__________CCCCCCCCCCCCCGGAGAAATAG GGGGGGGGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108557 Functional Loss DEL dbSNP153 33..42 33 - - - 109173 RMVar_ID_109173 Human_SNP_ID_625190335 m1A Human chr17 - 44569078 44569071 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC________CCCCCCCCCCCCCCCCGGAGAAATAG GGGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108567 Functional Loss DEL dbSNP153 32..39 33 - - - 109174 RMVar_ID_109174 Human_SNP_ID_625190339 m1A Human chr17 - 44569078 44569072 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC_______CCCCCCCCCCCCCCCCCGGAGAAATAG GGGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108573 Functional Loss DEL dbSNP153 32..38 33 - - - 109175 RMVar_ID_109175 Human_SNP_ID_625190342 m1A Human chr17 - 44569078 44569073 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC______CCCCCCCCCCCCCCCCCCGGAGAAATAG GGGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108577 Functional Loss DEL dbSNP153 32..37 33 - - - 109176 RMVar_ID_109176 Human_SNP_ID_625190347 m1A Human chr17 - 44569078 44569074 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCA____CCCCCCCCCCCCCCCCCCCGGAGAAATAG GGGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108582 Functional Loss DEL dbSNP153 33..36 33 - - - 109177 RMVar_ID_109177 Human_SNP_ID_625190348 m1A Human chr17 - 44569078 44569074 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC_____CCCCCCCCCCCCCCCCCCCGGAGAAATAG GGGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108583 Functional Loss DEL dbSNP153 32..36 33 - - - 109178 RMVar_ID_109178 Human_SNP_ID_625190351 m1A Human chr17 - 44569078 44569075 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCA___CCCCCCCCCCCCCCCCCCCCGGAGAAATAG GGGT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108586 Functional Loss DEL dbSNP153 33..35 33 - - - 109179 RMVar_ID_109179 Human_SNP_ID_625190352 m1A Human chr17 - 44569078 44569075 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC____CCCCCCCCCCCCCCCCCCCCGGAGAAATAG GGGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108590 Functional Loss DEL dbSNP153 32..35 33 - - - 109180 RMVar_ID_109180 Human_SNP_ID_625190353 m1A Human chr17 - 44569078 44569076 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC___CCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GGTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1446838553 Functional Loss DEL dbSNP153 32..34 33 - - - 109181 RMVar_ID_109181 Human_SNP_ID_625190356 m1A Human chr17 - 44569078 44569077 44569079 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCC__CCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GTT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs368004138 Functional Loss DEL dbSNP153 32..33 33 - - - 109182 RMVar_ID_109182 Human_SNP_ID_625190360 m1A Human chr17 - 44569078 44569077 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCA_CCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1568108599 Functional Loss DEL dbSNP153 33..33 33 - - - 109183 RMVar_ID_109183 Human_SNP_ID_625190362 m1A Human chr17 - 44569078 44569078 44569078 GAAAGAATAAAGCTTCCTCTCTCCACCCCCCAACCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG GAAAGAATAAAGCTTCCTCTCTCCACCCCCCACCCCCCCCCCCCCCCCCCCCCCCGGAGAAATAG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44569051..44569100 26863196 MeRIP-seq:(Medium) rs1338123216 Functional Loss SNV dbSNP153 33..33 33 - - - 109184 RMVar_ID_109184 Human_SNP_ID_625221140 m1A Human chr17 + 44689718 44689718 44689718 CCAAAGCCGCCGCCTCCGCCATCGCCTTCGCCAGGGGCTATCGCGGCCACTTCGCTGGGCGCCGC CCAAAGCCGCCGCCTCCGCCATCGCCTTCGCCGGGGGCTATCGCGGCCACTTCGCTGGGCGCCGC A G MEIOC Ensembl:ENSG00000180336 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:44689576..44689775;chr17:44689505..44689775;chr17:44689551..44689775 26863196 MeRIP-seq:(Medium) rs1478538335 Functional Loss SNV dbSNP153 33..33 33 - - - 109185 RMVar_ID_109185 Human_SNP_ID_625225801 m1A Human chr17 + 44708725 44708725 44708725 GAGATTGATGCTGTAGCTGCCCTGAGATAACCAGGACTGTGGAATCGGGAAGAGCTCATGGAGCT GAGATTGATGCTGTAGCTGCCCTGAGATAACCGGGACTGTGGAATCGGGAAGAGCTCATGGAGCT A G DBF4B Ensembl:ENSG00000161692 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:44708676..44722940;chr17:44708676..44709327 26863196 MeRIP-seq:(Medium) rs1228349091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491073,Human_RBP_ID_1534905,Human_RBP_ID_1859487,Human_RBP_ID_3524776,Human_RBP_ID_13026089,Human_RBP_ID_18419980,Human_RBP_ID_18699222,Human_RBP_ID_23728998,Human_RBP_ID_26331929,Human_RBP_ID_27813966 109186 RMVar_ID_109186 Human_SNP_ID_625225803 m1A Human chr17 - 44708730 44708729 44708731 TCGCGAGCTCCATGAGCTCTTCCCGATTCCACAGTCCTGGTTATCTCAGGGCAGCTACAGCATCA TCGCGAGCTCCATGAGCTCTTCCCGATTCCA__GTCCTGGTTATCTCAGGGCAGCTACAGCATCA CTG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44708662..44709390 26863196 MeRIP-seq:(Medium) rs1309753487 Functional Loss DEL dbSNP153 32..33 33 - - - 109187 RMVar_ID_109187 Human_SNP_ID_625234552 m1A Human chr17 + 44743044 44743044 44743044 AAATAGGAGGGAAAAAATTAAGGGAATGTGGCAGTAGATGAAATGGGAGCAAAGAGAGAAAGAGG AAATAGGAGGGAAAAAATTAAGGGAATGTGGCGGTAGATGAAATGGGAGCAAAGAGAGAAAGAGG A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44743035..44743242 26863196 MeRIP-seq:(Medium) rs758639644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69280,RMVar_hsa_circ_306723,RMVar_hsa_circ_184720,RMVar_hsa_circ_30496,RMVar_hsa_circ_30101 109188 RMVar_ID_109188 Human_SNP_ID_625236209 m1A Human chr17 - 44749244 44749242 44749244 TGGGGCTGGGGTTGGGACCAGGGCTGGGAGACAGGGAGACAGGGCACCTGGAGAGGCTGGGGGGC TGGGGCTGGGGTTGGGACCAGGGCTGGGAGAC__GGAGACAGGGCACCTGGAGAGGCTGGGGGGC CCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44749193..44749301 26863196 MeRIP-seq:(Medium) rs1362993113 Functional Loss DEL dbSNP153 33..34 33 - - - 109189 RMVar_ID_109189 Human_SNP_ID_625236382 m1A Human chr17 + 44749834 44749834 44749834 GTGCTCCACCCCCAACCCCGGCCTCCTTTCTCACGAGCATGTGGCCGCTCCTGCTTTCCAAAATG GTGCTCCACCCCCAACCCCGGCCTCCTTTCTCGCGAGCATGTGGCCGCTCCTGCTTTCCAAAATG A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44749760..44750242 26863196 MeRIP-seq:(Medium) rs1176074167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491091,Human_RBP_ID_18699253 109190 RMVar_ID_109190 Human_SNP_ID_625238869 m1A Human chr17 - 44759053 44759053 44759053 CCGGGCGGGGGTCGCGGAGAGGTGGGGGCGGCAGGGACGGCGCCGGGGCTCAGCGCGCTCCGGCC CCGGGCGGGGGTCGCGGAGAGGTGGGGGCGGCGGGGACGGCGCCGGGGCTCAGCGCGCTCCGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44759007..44759151 26863196 MeRIP-seq:(Medium) rs1234910107 Functional Loss SNV dbSNP153 33..33 33 - - - 109191 RMVar_ID_109191 Human_SNP_ID_625238877 m1A Human chr17 - 44759066 44759066 44759066 CGGGGGCGCGGGGCCGGGCGGGGGTCGCGGAGAGGTGGGGGCGGCAGGGACGGCGCCGGGGCTCA CGGGGGCGCGGGGCCGGGCGGGGGTCGCGGAGGGGTGGGGGCGGCAGGGACGGCGCCGGGGCTCA T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:44759001..44759125 26863410 MeRIP-seq:(Medium) rs1199079072 Functional Loss SNV dbSNP153 33..33 33 - - - 109192 RMVar_ID_109192 Human_SNP_ID_625238881 m1A Human chr17 + 44759074 44759074 44759074 GGCGCCGTCCCTGCCGCCCCCACCTCTCCGCGACCCCCGCCCGGCCCCGCGCCCCCGCCCCGGCT GGCGCCGTCCCTGCCGCCCCCACCTCTCCGCGCCCCCCGCCCGGCCCCGCGCCCCCGCCCCGGCT A C ADAM11 Ensembl:ENSG00000073670 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:44759001..44759250 26863410 MeRIP-seq:(Medium) rs888310235 Functional Loss SNV dbSNP153 33..33 33 - - - 109193 RMVar_ID_109193 Human_SNP_ID_625238894 m1A Human chr17 - 44759106 44759106 44759106 CAGGGACGGGGGTGGGGAGGCGCCAGCTGCGGAGCCGGGGCGGGGGCGCGGGGCCGGGCGGGGGT CAGGGACGGGGGTGGGGAGGCGCCAGCTGCGGGGCCGGGGCGGGGGCGCGGGGCCGGGCGGGGGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44759001..44759181 26863410 MeRIP-seq:(Medium) rs1178433520 Functional Loss SNV dbSNP153 33..33 33 - - - 109194 RMVar_ID_109194 Human_SNP_ID_625250723 m1A Human chr17 - 44801664 44801664 44801664 AGGAGGCAGAGGTTGCAGTGAGCTGAGATCATACCATTGCACTCCAGCCTGCAAGACAGAGTGAA AGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGCAAGACAGAGTGAA T C GJC1 Ensembl:ENSG00000182963 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs566348485 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_139,Clinvar_Rec_712 RMVar_hsa_circ_77653,RMVar_hsa_circ_102483,RMVar_hsa_circ_122658,RMVar_hsa_circ_85519,RMVar_hsa_circ_184725,RMVar_hsa_circ_184726,RMVar_hsa_circ_184727,RMVar_hsa_circ_184724 109195 RMVar_ID_109195 Human_SNP_ID_625250726 m1A Human chr17 - 44801696 44801696 44801696 GGGAGGTTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCATA GGGAGGTTGAGGCAGGAGAATTGCTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCTGAGATCATA T G GJC1 Ensembl:ENSG00000182963 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1250942614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77653,RMVar_hsa_circ_102483,RMVar_hsa_circ_122658,RMVar_hsa_circ_85519,RMVar_hsa_circ_184725,RMVar_hsa_circ_184726,RMVar_hsa_circ_184727,RMVar_hsa_circ_184724 109196 RMVar_ID_109196 Human_SNP_ID_625251525 m1A Human chr17 + 44805338 44805338 44805338 TCTTCCCGAATCCGTCGTCGGCCATCATGCTTAGGTTTGGGTTGGCTCTGCTCTTTATTTTCCTT TCTTCCCGAATCCGTCGTCGGCCATCATGCTTCGGTTTGGGTTGGCTCTGCTCTTTATTTTCCTT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44805251..44805504 26863196 MeRIP-seq:(Medium) rs769654327 Functional Loss SNV dbSNP153 33..33 33 - - - 109197 RMVar_ID_109197 Human_SNP_ID_625251526 m1A Human chr17 + 44805338 44805338 44805338 TCTTCCCGAATCCGTCGTCGGCCATCATGCTTAGGTTTGGGTTGGCTCTGCTCTTTATTTTCCTT TCTTCCCGAATCCGTCGTCGGCCATCATGCTTGGGTTTGGGTTGGCTCTGCTCTTTATTTTCCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44805251..44805504 26863196 MeRIP-seq:(Medium) rs769654327 Functional Loss SNV dbSNP153 33..33 33 - - - 109198 RMVar_ID_109198 Human_SNP_ID_625251573 m1A Human chr17 - 44805474 44805474 44805474 CGGTGAAGCAGACAAGAAGGCAGCTCGGAGCAAGCCCTATGCAATGCGCTGGAAACAACACCGGG CGGTGAAGCAGACAAGAAGGCAGCTCGGAGCACGCCCTATGCAATGCGCTGGAAACAACACCGGG T G GJC1 Ensembl:ENSG00000182963 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44805426..44805550 32194978 MeRIP-seq:(Medium) rs1417068746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18439090 RMVar_hsa_circ_77653,RMVar_hsa_circ_102483,RMVar_hsa_circ_122658,RMVar_hsa_circ_85519,RMVar_hsa_circ_184725,RMVar_hsa_circ_184726,RMVar_hsa_circ_184727,RMVar_hsa_circ_184724,RMVar_hsa_circ_184730,RMVar_hsa_circ_184731 109199 RMVar_ID_109199 Human_SNP_ID_625258483 m1A Human chr17 - 44830255 44830231 44830256 GCCTTCCCGCGGGTCGCGGCGGCGGGAGCGGGAGGCGGCGGCGGCGGCGGCAGCGGCGGGAGCGG GCCTTCCCGCGGGTCGCGGCGGCGGGAGCGG_________________________CGGGAGCGG GCCGCTGCCGCCGCCGCCGCCGCCTC G GJC1 Ensembl:ENSG00000182963 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:44830176..44830262 26863410 MeRIP-seq:(Medium) rs1382643554 Functional Loss DEL dbSNP153 32..56 33 - - - RMVar_hsa_circ_122658,RMVar_hsa_circ_184727 109200 RMVar_ID_109200 Human_SNP_ID_625276939 m1A Human chr17 + 44901079 44901079 44901079 CAGGCTGCACTCACTGCTGATGAGAAGTACAAACGGGAGAATGCTGCCAAGTTACGGGCAGTGGA CAGGCTGCACTCACTGCTGATGAGAAGTACAAGCGGGAGAATGCTGCCAAGTTACGGGCAGTGGA A G CCDC103,FAM187A Ensembl:ENSG00000167131,Ensembl:ENSG00000214447 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44900963..44901109 26863196 MeRIP-seq:(Medium) rs1567763166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1827416,Human_Splice_Rec_1827417,Human_Splice_Rec_1827420,Human_Splice_Rec_1827421,Human_Splice_Rec_1827426,Human_Splice_Rec_1827427,Human_Splice_Rec_1827432,Human_Splice_Rec_1827433,Human_Splice_Rec_1827438,Human_Splice_Rec_1827439,Human_Splice_Rec_1827444,Human_Splice_Rec_1827445,Human_Splice_Rec_1827450,Human_Splice_Rec_1827451 109201 RMVar_ID_109201 Human_SNP_ID_625277342 m1A Human chr17 + 44902549 44902549 44902549 TCTTGGGGAGCTGCTGGTGGCACTGGCTGATCACGTGGGGCCGGCTGACCGGGCAGCGGTGCTGG TCTTGGGGAGCTGCTGGTGGCACTGGCTGATCCCGTGGGGCCGGCTGACCGGGCAGCGGTGCTGG A C CCDC103,FAM187A Ensembl:ENSG00000167131,Ensembl:ENSG00000214447 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:44902542..44902857 26863196 MeRIP-seq:(Medium) rs145457535 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_713 GWAS_ID_15260,GWAS_ID_15261,GWAS_ID_15262,GWAS_ID_15263 109202 RMVar_ID_109202 Human_SNP_ID_625285859 m1A Human chr17 - 44932961 44932961 44932961 ATCTCAGCTGAAGAGCAATGTGACCAGCCTGGACTGTCACATCAGCCAGTATGCTACCATCTGCC ATCTCAGCTGAAGAGCAATGTGACCAGCCTGGTCTGTCACATCAGCCAGTATGCTACCATCTGCC T A KIF18B Ensembl:ENSG00000186185 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44932901..44932975 26863196 MeRIP-seq:(Medium) rs1290685320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_278282,Human_RBP_ID_896621,Human_RBP_ID_1008533,Human_RBP_ID_1535052,Human_RBP_ID_1859666,Human_RBP_ID_3952544,Human_RBP_ID_5466563,Human_RBP_ID_6600307,Human_RBP_ID_8818641,Human_RBP_ID_9287630,Human_RBP_ID_17893695,Human_RBP_ID_18699461 Human_Splice_Rec_1827754,Human_Splice_Rec_1827755,Human_Splice_Rec_1827782,Human_Splice_Rec_1827783,Human_Splice_Rec_1827810,Human_Splice_Rec_1827811,Human_Splice_Rec_1827826,Human_Splice_Rec_1827827 Human_miRNA_ID_2332942,Human_miRNA_ID_2657593,Human_miRNA_ID_2878001,Human_miRNA_ID_2966026 RMVar_hsa_circ_31547,RMVar_hsa_circ_371371,RMVar_hsa_circ_74048,RMVar_hsa_circ_184772,RMVar_hsa_circ_11210,RMVar_hsa_circ_53280 109203 RMVar_ID_109203 Human_SNP_ID_625289939 m1A Human chr17 + 44947693 44947693 44947693 TTGCTCACGGGTCCCACAGCCACACCACAGACAGCAGTACCCACACCGGGAGAGAGCGCCCCACA TTGCTCACGGGTCCCACAGCCACACCACAGACGGCAGTACCCACACCGGGAGAGAGCGCCCCACA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44947563..44947725 26863196 MeRIP-seq:(Medium) rs1483347972 Functional Loss SNV dbSNP153 33..33 33 - - - 109204 RMVar_ID_109204 Human_SNP_ID_625289946 m1A Human chr17 + 44947711 44947711 44947711 GCCACACCACAGACAGCAGTACCCACACCGGGAGAGAGCGCCCCACACCCTCCCCTACCCGCGCC GCCACACCACAGACAGCAGTACCCACACCGGGTGAGAGCGCCCCACACCCTCCCCTACCCGCGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr17:44936201..44947775;chr17:44947518..44947742 26863196 MeRIP-seq:(Medium) rs1460121763 Functional Loss SNV dbSNP153 33..33 33 - - - 109205 RMVar_ID_109205 Human_SNP_ID_625294933 m1A Human chr17 + 44967539 44967539 44967539 AGGACATGGTAGGTGAAAAAGTAGGTGCCGGGAATGTTGCACGTAAACTTGCCGCTGGCCGCGTC AGGACATGGTAGGTGAAAAAGTAGGTGCCGGGGATGTTGCACGTAAACTTGCCGCTGGCCGCGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44967446..44967755 26863196 MeRIP-seq:(Medium) rs748894893 Functional Loss SNV dbSNP153 33..33 33 - - - 109206 RMVar_ID_109206 Human_SNP_ID_625294983 m1A Human chr17 + 44967660 44967660 44967660 CGTGGGGGTTCTTGAGGCCGGCGTAGAAGGCCACGCGCGGCACCGTGGTGTAGGTGGCAGTGCTG CGTGGGGGTTCTTGAGGCCGGCGTAGAAGGCCTCGCGCGGCACCGTGGTGTAGGTGGCAGTGCTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44967615..44967808 26863196 MeRIP-seq:(Medium) rs769883503 Functional Loss SNV dbSNP153 33..33 33 - - - 109207 RMVar_ID_109207 Human_SNP_ID_625295110 m1A Human chr17 - 44967970 44967970 44967970 GCGGCCCGGAAGGCCACTATGAGATGCTGGGCACCTGCCGCATGGTGTGCGACCCCTACCCCGCG GCGGCCCGGAAGGCCACTATGAGATGCTGGGCCCCTGCCGCATGGTGTGCGACCCCTACCCCGCG T G C1QL1 Ensembl:ENSG00000131094 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44967922..44968298 26863196 MeRIP-seq:(Medium) rs770780187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491253 109208 RMVar_ID_109208 Human_SNP_ID_625295118 m1A Human chr17 - 44967992 44967992 44967992 ATCCCCGTGCTGGTGAGCTCGGGCGGCCCGGAAGGCCACTATGAGATGCTGGGCACCTGCCGCAT ATCCCCGTGCTGGTGAGCTCGGGCGGCCCGGACGGCCACTATGAGATGCTGGGCACCTGCCGCAT T G C1QL1 Ensembl:ENSG00000131094 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44967851..44968333 26863196 MeRIP-seq:(Medium) rs1461774723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4432078 109209 RMVar_ID_109209 Human_SNP_ID_540576026 m1A Human chr13 - 91347812 91347812 91347812 CGGCCCGCCCCGCGAGGAGAGCTTCGCGGAGGAGCGCGAGCCCCGGCGGCGCTGCGGTAGTCGTC CGGCCCGCCCCGCGAGGAGAGCTTCGCGGAGGGGCGCGAGCCCCGGCGGCGCTGCGGTAGTCGTC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:91347734..91348071 26863196 MeRIP-seq:(Medium) rs1486843677 Functional Loss SNV dbSNP153 33..33 33 - - - 109210 RMVar_ID_109210 Human_SNP_ID_540576056 m1A Human chr13 + 91347890 91347890 91347890 CCGGCCTGGGGCCTCCGGTCGTAGTAAAGCGCAGGCGGGCGGGGAGGCGGGAGCAGGAGCCCGCG CCGGCCTGGGGCCTCCGGTCGTAGTAAAGCGCGGGCGGGCGGGGAGGCGGGAGCAGGAGCCCGCG A G MIR17HG Ensembl:ENSG00000215417 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:91347764..91348056 26863196 MeRIP-seq:(Medium) rs1306631685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230756,Human_RBP_ID_3438761,Human_RBP_ID_5087543,Human_RBP_ID_5235882,Human_RBP_ID_5561762,Human_RBP_ID_8075108,Human_RBP_ID_8180354,Human_RBP_ID_8249538,Human_RBP_ID_9323485,Human_RBP_ID_17114787,Human_RBP_ID_17360759,Human_RBP_ID_18160691,Human_RBP_ID_18417737,Human_RBP_ID_18480056,Human_RBP_ID_22369937,Human_RBP_ID_22710658,Human_RBP_ID_22737241,Human_RBP_ID_27572089 Human_Splice_Rec_1474821,Human_Splice_Rec_1474823,Human_Splice_Rec_1474829 109211 RMVar_ID_109211 Human_SNP_ID_540576062 m1A Human chr13 + 91347912 91347912 91347912 AGTAAAGCGCAGGCGGGCGGGGAGGCGGGAGCAGGAGCCCGCGGCCGGCCAGCCGAAGATGGTGG AGTAAAGCGCAGGCGGGCGGGGAGGCGGGAGCGGGAGCCCGCGGCCGGCCAGCCGAAGATGGTGG A G MIR17HG Ensembl:ENSG00000215417 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:91347705..91349708 26863196 MeRIP-seq:(Medium) rs1166399045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230756,Human_RBP_ID_3438761,Human_RBP_ID_5087543,Human_RBP_ID_5235882,Human_RBP_ID_5351122,Human_RBP_ID_5645615,Human_RBP_ID_8075108,Human_RBP_ID_8180354,Human_RBP_ID_8230180,Human_RBP_ID_8249538,Human_RBP_ID_9323485,Human_RBP_ID_9417311,Human_RBP_ID_17114787,Human_RBP_ID_17360759,Human_RBP_ID_18160691,Human_RBP_ID_18189322,Human_RBP_ID_18417737,Human_RBP_ID_18480056,Human_RBP_ID_22369937,Human_RBP_ID_22710658,Human_RBP_ID_22737241,Human_RBP_ID_24366314,Human_RBP_ID_24558120,Human_RBP_ID_26777759,Human_RBP_ID_27572089 Human_Splice_Rec_1474821,Human_Splice_Rec_1474823,Human_Splice_Rec_1474829 109212 RMVar_ID_109212 Human_SNP_ID_540576223 m1A Human chr13 + 91348227 91348227 91348227 GGGGCGGCGTGCGCGTGGCGGCCGCGCCCGGGACCCGCGCAGACCCTGCCTGGGCCGACCCGAAG GGGGCGGCGTGCGCGTGGCGGCCGCGCCCGGGTCCCGCGCAGACCCTGCCTGGGCCGACCCGAAG A T MIR17HG Ensembl:ENSG00000215417 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:91348044..91348314 26863196 MeRIP-seq:(Medium) rs902664798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3994,Human_RBP_ID_230757,Human_RBP_ID_260501,Human_RBP_ID_812022,Human_RBP_ID_879739,Human_RBP_ID_1487135,Human_RBP_ID_3438765,Human_RBP_ID_4277037,Human_RBP_ID_5087573,Human_RBP_ID_5140483,Human_RBP_ID_5235884,Human_RBP_ID_5315337,Human_RBP_ID_5350624,Human_RBP_ID_5645469,Human_RBP_ID_8075110,Human_RBP_ID_8180108,Human_RBP_ID_8230132,Human_RBP_ID_8249181,Human_RBP_ID_8725595,Human_RBP_ID_8940954,Human_RBP_ID_9281299,Human_RBP_ID_9323490,Human_RBP_ID_9340807,Human_RBP_ID_9417178,Human_RBP_ID_17114789,Human_RBP_ID_17360761,Human_RBP_ID_17477975,Human_RBP_ID_18160694,Human_RBP_ID_18417738,Human_RBP_ID_18480062,Human_RBP_ID_18936096,Human_RBP_ID_22369940,Human_RBP_ID_22414889,Human_RBP_ID_22426172,Human_RBP_ID_22472588,Human_RBP_ID_22539573,Human_RBP_ID_22696155,Human_RBP_ID_22710660,Human_RBP_ID_22737243,Human_RBP_ID_24366315,Human_RBP_ID_24409811,Human_RBP_ID_25067893,Human_RBP_ID_26756145,Human_RBP_ID_26777761,Human_RBP_ID_26919118,Human_RBP_ID_27572091,Human_RBP_ID_27837112 109213 RMVar_ID_109213 Human_SNP_ID_540589550 m1A Human chr13 - 91398689 91398656 91398689 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGCC_________________________________ CGGAGGCGGCGGCGGCGGCGGCAGTGGCGGCAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs1566361346 Functional Loss DEL dbSNP153 33..65 33 - - - 109214 RMVar_ID_109214 Human_SNP_ID_540589579 m1A Human chr13 - 91398689 91398671 91398689 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGCC__________________GCCGCCGCCGCCTCC CGGCGGCAGTGGCGGCAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs60533993 Functional Loss DEL dbSNP153 33..50 33 - - - 109215 RMVar_ID_109215 Human_SNP_ID_540589580 m1A Human chr13 - 91398689 91398671 91398689 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGCC_________ACTGCCGCCGCCGCCGCCGCCTCC CGGCGGCAGTGGCGGCAGT CGGCGGCAGT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs60533993 Functional Loss DEL dbSNP153 33..41 33 - - - 109216 RMVar_ID_109216 Human_SNP_ID_540589582 m1A Human chr13 + 91398705 91398672 91398705 GCGGCAGTGGCGGCAGTGGCGGCAGTGGCGGCAGCGGCAGCAGTTGCAGCAGTGGTGGCCAGAGC _________________________________GCGGCAGCAGTTGCAGCAGTGGTGGCCAGAGC GGCGGCAGTGGCGGCAGTGGCGGCAGTGGCGGCA G GPC5 Ensembl:ENSG00000179399 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:91398655..91398766;chr13:91398656..91398868 26863196 MeRIP-seq:(Medium) rs1321746534 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_164034 109217 RMVar_ID_109217 Human_SNP_ID_540589591 m1A Human chr13 - 91398689 91398683 91398689 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGCC______GCCACTGCCGCCGCCGCCGCCGCCTCC CGGCAGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs1257275574 Functional Loss DEL dbSNP153 33..38 33 - - - 109218 RMVar_ID_109218 Human_SNP_ID_540589595 m1A Human chr13 - 91398689 91398687 91398690 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGC___TGCCGCCACTGCCGCCGCCGCCGCCGCCTCC AGTG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs1566361492 Functional Loss DEL dbSNP153 32..34 33 - - - 109219 RMVar_ID_109219 Human_SNP_ID_540589596 m1A Human chr13 - 91398689 91398689 91398689 CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCACTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC CTGCAACTGCTGCCGCTGCCGCCACTGCCGCCGCTGCCGCCACTGCCGCCGCCGCCGCCGCCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91398642..91398790 26863196 MeRIP-seq:(Medium) rs908808310 Functional Loss SNV dbSNP153 33..33 33 - - - 109220 RMVar_ID_109220 Human_SNP_ID_540589620 m1A Human chr13 + 91398705 91398705 91398705 GCGGCAGTGGCGGCAGTGGCGGCAGTGGCGGCAGCGGCAGCAGTTGCAGCAGTGGTGGCCAGAGC GCGGCAGTGGCGGCAGTGGCGGCAGTGGCGGCGGCGGCAGCAGTTGCAGCAGTGGTGGCCAGAGC A G GPC5 Ensembl:ENSG00000179399 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:91398655..91398766;chr13:91398656..91398868 26863196 MeRIP-seq:(Medium) rs1333317526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164034 109221 RMVar_ID_109221 Human_SNP_ID_541089721 m1A Human chr13 - 93387315 93387315 93387315 GGGCCTGTTGGGGGTGGAGGGGAAGGGGAGGAAGAGCATTAGTACAGGTACCTGGTGCATGCGGG GGGCCTGTTGGGGGTGGAGGGGAAGGGGAGGAGGAGCATTAGTACAGGTACCTGGTGCATGCGGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:93387282..93387395 26863196 MeRIP-seq:(Medium) rs1461210605 Functional Loss SNV dbSNP153 33..33 33 - - - 109222 RMVar_ID_109222 Human_SNP_ID_541374283 m1A Human chr13 - 94549665 94549665 94549665 GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCAGCTACTTTTAAATTCTG GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGTTCCCGGGTTTCGGCAGCTACTTTTAAATTCTG T A TRF-GAA1-1,TRF-GAA1-1:2,piR-43773,tRNA-Phe-GAA-1-3 RNACentral:URS0000632456,RNACentral:URS00001CE4E0,RNACentral:URS00004CEA14,RNACentral:URS000029CCC5 tRNA,tRNA,piRNA,tRNA intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs990767887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_440145,Human_RBP_ID_1170599,Human_RBP_ID_1487320,Human_RBP_ID_1813153,Human_RBP_ID_4279952,Human_RBP_ID_5462992,Human_RBP_ID_5493046,Human_RBP_ID_6309458,Human_RBP_ID_8248953,Human_RBP_ID_8397135,Human_RBP_ID_12239718,Human_RBP_ID_17361183,Human_RBP_ID_17587120,Human_RBP_ID_17842781,Human_RBP_ID_18643572,Human_RBP_ID_21922124,Human_RBP_ID_22796840,Human_RBP_ID_23126443,Human_RBP_ID_23607783,Human_RBP_ID_26919710,Human_RBP_ID_27642242 109223 RMVar_ID_109223 Human_SNP_ID_541374284 m1A Human chr13 - 94549665 94549665 94549665 GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCAGCTACTTTTAAATTCTG GTTAGACTGAAGATCTAAAGGTCCCTGGTTCGGTCCCGGGTTTCGGCAGCTACTTTTAAATTCTG T C TRF-GAA1-1,TRF-GAA1-1:2,piR-43773,tRNA-Phe-GAA-1-3 RNACentral:URS0000632456,RNACentral:URS00001CE4E0,RNACentral:URS00004CEA14,RNACentral:URS000029CCC5 tRNA,tRNA,piRNA,tRNA intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs990767887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_440145,Human_RBP_ID_1170599,Human_RBP_ID_1487320,Human_RBP_ID_1813153,Human_RBP_ID_4279952,Human_RBP_ID_5462992,Human_RBP_ID_5493046,Human_RBP_ID_6309458,Human_RBP_ID_8248953,Human_RBP_ID_8397135,Human_RBP_ID_12239718,Human_RBP_ID_17361183,Human_RBP_ID_17587120,Human_RBP_ID_17842781,Human_RBP_ID_18643572,Human_RBP_ID_21922124,Human_RBP_ID_22796840,Human_RBP_ID_23126443,Human_RBP_ID_23607783,Human_RBP_ID_26919710,Human_RBP_ID_27642242 109224 RMVar_ID_109224 Human_SNP_ID_541393835 m1A Human chr13 + 94628669 94628669 94628669 ATGACAAAGTTACCAAGTTCAACCTGCTCATTAAATCATCTCTCTATTAGTTCTTTGTAAATCAC ATGACAAAGTTACCAAGTTCAACCTGCTCATTTAATCATCTCTCTATTAGTTCTTTGTAAATCAC A T GPR180 Ensembl:ENSG00000152749 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2298057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_440265,Human_RBP_ID_12241276,Human_RBP_ID_16995877,Human_RBP_ID_17245534,Human_RBP_ID_17360505,Human_RBP_ID_17477652 Human_miRNA_ID_300836,Human_miRNA_ID_433688 GWAS_ID_15264,GWAS_ID_15265,GWAS_ID_15266,GWAS_ID_15267,GWAS_ID_15268,GWAS_ID_15269,GWAS_ID_15270,GWAS_ID_15271,GWAS_ID_15272,GWAS_ID_15273,GWAS_ID_15274,GWAS_ID_15275,GWAS_ID_15276,GWAS_ID_15277,GWAS_ID_15278,GWAS_ID_15279,GWAS_ID_15280,GWAS_ID_15281,GWAS_ID_15282,GWAS_ID_15283,GWAS_ID_15284,GWAS_ID_15285,GWAS_ID_15286,GWAS_ID_15287,GWAS_ID_15288,GWAS_ID_15289,GWAS_ID_15290,GWAS_ID_15291,GWAS_ID_15292,GWAS_ID_15293,GWAS_ID_15294,GWAS_ID_15295 109225 RMVar_ID_109225 Human_SNP_ID_541544432 m1A Human chr13 - 95244797 95244797 95244797 TACTGCTTAGCAGCAGCAGTGCTAGTAGAAGCAGCAGCAGGATTAGTAGTGGTTGGTACTCAGTA TACTGCTTAGCAGCAGCAGTGCTAGTAGAAGCCGCAGCAGGATTAGTAGTGGTTGGTACTCAGTA T G ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:95244788..95245026 26863196 MeRIP-seq:(Medium) rs1463859948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12242468 RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_28224,RMVar_hsa_circ_267547,RMVar_hsa_circ_81497,RMVar_hsa_circ_356247,RMVar_hsa_circ_164124,RMVar_hsa_circ_164125,RMVar_hsa_circ_91016,RMVar_hsa_circ_286939,RMVar_hsa_circ_164127,RMVar_hsa_circ_164128 109226 RMVar_ID_109226 Human_SNP_ID_541558717 m1A Human chr13 - 95301317 95301317 95301317 CGCGACCCCGGCCCGCGCCCGCCCCGCCCGGCAAGATGCTGCCCGTGTACCAGGAGGTGAAGCCC CGCGACCCCGGCCCGCGCCCGCCCCGCCCGGCCAGATGCTGCCCGTGTACCAGGAGGTGAAGCCC T G ABCC4 Ensembl:ENSG00000125257 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:95301284..95301389 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_4275325 Human_Splice_Rec_1475065,Human_Splice_Rec_1475125,Human_Splice_Rec_1475187,Human_Splice_Rec_1475251,Human_Splice_Rec_1475335,Human_Splice_Rec_1475379,Human_Splice_Rec_1475417,Human_Splice_Rec_1475459,Human_Splice_Rec_1475499,Human_Splice_Rec_1475531,Human_Splice_Rec_1475561 RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 109227 RMVar_ID_109227 Human_SNP_ID_541558843 m1A Human chr13 - 95301631 95301631 95301631 GGGCGTAGCTCTGGGCTCCCTTTGGCGTCGCCAGCTTCGCCTCCTCCCGCCGCGTCTCCTCCCGC GGGCGTAGCTCTGGGCTCCCTTTGGCGTCGCCTGCTTCGCCTCCTCCCGCCGCGTCTCCTCCCGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:95301580..95301770 26863196 MeRIP-seq:(Medium) rs1027291292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18435426,Human_RBP_ID_18643673 109228 RMVar_ID_109228 Human_SNP_ID_541558844 m1A Human chr13 - 95301631 95301631 95301631 GGGCGTAGCTCTGGGCTCCCTTTGGCGTCGCCAGCTTCGCCTCCTCCCGCCGCGTCTCCTCCCGC GGGCGTAGCTCTGGGCTCCCTTTGGCGTCGCCGGCTTCGCCTCCTCCCGCCGCGTCTCCTCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:95301580..95301770 26863196 MeRIP-seq:(Medium) rs1027291292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18435426,Human_RBP_ID_18643673 109229 RMVar_ID_109229 Human_SNP_ID_541641051 m1A Human chr13 - 95630014 95630014 95630014 GCTCACCAGGTCTGAGCTAGAGGCTGCACACCATGCCAGTGCAGTCAGATTCTCCAAGGTACCAG GCTCACCAGGTCTGAGCTAGAGGCTGCACACCGTGCCAGTGCAGTCAGATTCTCCAAGGTACCAG T C DZIP1 Ensembl:ENSG00000134874 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:95624910..95630719 32194978 MeRIP-seq:(Medium) rs184350900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_879502,Human_RBP_ID_22919087 Human_Splice_Rec_1475622,Human_Splice_Rec_1475623,Human_Splice_Rec_1475660,Human_Splice_Rec_1475661,Human_Splice_Rec_1475700,Human_Splice_Rec_1475701,Human_Splice_Rec_1475742,Human_Splice_Rec_1475743,Human_Splice_Rec_1475790,Human_Splice_Rec_1475791 RMVar_hsa_circ_3644,RMVar_hsa_circ_266932,RMVar_hsa_circ_41962,RMVar_hsa_circ_5337,RMVar_hsa_circ_31348,RMVar_hsa_circ_24612,RMVar_hsa_circ_4599,RMVar_hsa_circ_293530,RMVar_hsa_circ_34160,RMVar_hsa_circ_164141,RMVar_hsa_circ_32667,RMVar_hsa_circ_274637,RMVar_hsa_circ_164147,RMVar_hsa_circ_164144,RMVar_hsa_circ_164145,RMVar_hsa_circ_335245,RMVar_hsa_circ_164149,RMVar_hsa_circ_164148,RMVar_hsa_circ_306825,RMVar_hsa_circ_285677,RMVar_hsa_circ_164150,RMVar_hsa_circ_285182 109230 RMVar_ID_109230 Human_SNP_ID_541641690 m1A Human chr13 - 95632692 95632692 95632692 AAGTGCTGGGGGCCTGATCACAGGAAGCCGTGAAGGCGTGGGCTGGAATGTGGAGTTTTTATATG AAGTGCTGGGGGCCTGATCACAGGAAGCCGTGGAGGCGTGGGCTGGAATGTGGAGTTTTTATATG T C DZIP1 Ensembl:ENSG00000134874 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:95632671..95632849 26863196 MeRIP-seq:(Medium) rs1266652023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266932,RMVar_hsa_circ_41962,RMVar_hsa_circ_5337,RMVar_hsa_circ_31348,RMVar_hsa_circ_4599,RMVar_hsa_circ_293530,RMVar_hsa_circ_164141,RMVar_hsa_circ_32667,RMVar_hsa_circ_274637,RMVar_hsa_circ_164147,RMVar_hsa_circ_164144,RMVar_hsa_circ_164145,RMVar_hsa_circ_335245,RMVar_hsa_circ_164149,RMVar_hsa_circ_164148,RMVar_hsa_circ_306825,RMVar_hsa_circ_285677,RMVar_hsa_circ_164150,RMVar_hsa_circ_285182 109231 RMVar_ID_109231 Human_SNP_ID_541644919 m1A Human chr13 + 95644503 95644503 95644503 GGGCCCGCGGAGGCCGAGGAGCAGCAAAGCGGAGAGAGGCAGGCCGGCTCCTTCTTGCAGGGCGC GGGCCCGCGGAGGCCGAGGAGCAGCAAAGCGGCGAGAGGCAGGCCGGCTCCTTCTTGCAGGGCGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:95643675..95644626 26863196 MeRIP-seq:(Medium) rs1263896632 Functional Loss SNV dbSNP153 33..33 33 - - - 109232 RMVar_ID_109232 Human_SNP_ID_541652649 m1A Human chr13 + 95676642 95676642 95676642 TGTTCCGGGACGCTCAGCGGGAGGCGGTTTTTACCGGCTCACTCGAGACCCCAATTCCAGGCGCC TGTTCCGGGACGCTCAGCGGGAGGCGGTTTTTCCCGGCTCACTCGAGACCCCAATTCCAGGCGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:95676596..95676879 26863196 MeRIP-seq:(Medium) rs1023055292 Functional Loss SNV dbSNP153 33..33 33 - - - 109233 RMVar_ID_109233 Human_SNP_ID_541652650 m1A Human chr13 + 95676642 95676642 95676642 TGTTCCGGGACGCTCAGCGGGAGGCGGTTTTTACCGGCTCACTCGAGACCCCAATTCCAGGCGCC TGTTCCGGGACGCTCAGCGGGAGGCGGTTTTTGCCGGCTCACTCGAGACCCCAATTCCAGGCGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:95676596..95676879 26863196 MeRIP-seq:(Medium) rs1023055292 Functional Loss SNV dbSNP153 33..33 33 - - - 109234 RMVar_ID_109234 Human_SNP_ID_541652664 m1A Human chr13 - 95676676 95676676 95676676 AACACGGTCCCGGGGAGTCTGAGGGAAGCTGCAGGGCGCCTGGAATTGGGGTCTCGAGTGAGCCG AACACGGTCCCGGGGAGTCTGAGGGAAGCTGCTGGGCGCCTGGAATTGGGGTCTCGAGTGAGCCG T A DNAJC3-DT Ensembl:ENSG00000247400 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:95676630..95676826 26863196 MeRIP-seq:(Medium) rs1029216752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812027,Human_RBP_ID_879765,Human_RBP_ID_4277049,Human_RBP_ID_5095160 109235 RMVar_ID_109235 Human_SNP_ID_541652916 m1A Human chr13 + 95677218 95677218 95677218 GCTGCCGGAGCGCCGGCGCGTGCTGGTGGGCCACACACCTTTCCTCCTCTTCACTCGCGAGCCCT GCTGCCGGAGCGCCGGCGCGTGCTGGTGGGCCTCACACCTTTCCTCCTCTTCACTCGCGAGCCCT A T DNAJC3 Ensembl:ENSG00000102580 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:95677167..95677266 26863196 MeRIP-seq:(Medium) rs952875604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230573,Human_RBP_ID_4276484,Human_RBP_ID_5274214,Human_RBP_ID_5417883,Human_RBP_ID_5438732,Human_RBP_ID_5462999,Human_RBP_ID_5493062,Human_RBP_ID_8074928,Human_RBP_ID_27428978 109236 RMVar_ID_109236 Human_SNP_ID_541652918 m1A Human chr13 + 95677222 95677222 95677222 CCGGAGCGCCGGCGCGTGCTGGTGGGCCACACACCTTTCCTCCTCTTCACTCGCGAGCCCTCGGA CCGGAGCGCCGGCGCGTGCTGGTGGGCCACACGCCTTTCCTCCTCTTCACTCGCGAGCCCTCGGA A G DNAJC3 Ensembl:ENSG00000102580 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:95677172..95677282 26863196 MeRIP-seq:(Medium) rs984646402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276484,Human_RBP_ID_5274214,Human_RBP_ID_5417883,Human_RBP_ID_5438732,Human_RBP_ID_5462999,Human_RBP_ID_5493062,Human_RBP_ID_8074928,Human_RBP_ID_26919412,Human_RBP_ID_27428978 109237 RMVar_ID_109237 Human_SNP_ID_541706983 m1A Human chr13 - 95897966 95897966 95897966 TTACTGTGGATCAAGGTGAGGAAGGCTGCAGGATGAGTGAGGTTGTCAGGAGCAGTATAAGAAGA TTACTGTGGATCAAGGTGAGGAAGGCTGCAGGGTGAGTGAGGTTGTCAGGAGCAGTATAAGAAGA T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:95897917..95898140 26863196 MeRIP-seq:(Medium) rs1428340050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6311168,Human_RBP_ID_12244915 RMVar_hsa_circ_2789,RMVar_hsa_circ_335904,RMVar_hsa_circ_317370,RMVar_hsa_circ_127695,RMVar_hsa_circ_19524,RMVar_hsa_circ_164163,RMVar_hsa_circ_164164,RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_13291,RMVar_hsa_circ_164176,RMVar_hsa_circ_71756,RMVar_hsa_circ_164178,RMVar_hsa_circ_341500,RMVar_hsa_circ_351932,RMVar_hsa_circ_340667,RMVar_hsa_circ_324538,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_51059,RMVar_hsa_circ_164185,RMVar_hsa_circ_164186,RMVar_hsa_circ_164188,RMVar_hsa_circ_105805,RMVar_hsa_circ_368361,RMVar_hsa_circ_164189,RMVar_hsa_circ_281967,RMVar_hsa_circ_279785,RMVar_hsa_circ_7299,RMVar_hsa_circ_164190,RMVar_hsa_circ_33570,RMVar_hsa_circ_164194,RMVar_hsa_circ_332069,RMVar_hsa_circ_50837,RMVar_hsa_circ_164193,RMVar_hsa_circ_42703,RMVar_hsa_circ_71035,RMVar_hsa_circ_124797,RMVar_hsa_circ_111503,RMVar_hsa_circ_164195,RMVar_hsa_circ_164196 109238 RMVar_ID_109238 Human_SNP_ID_541756000 m1A Human chr13 - 96090939 96090939 96090939 AGTTGGTGCAGGAGCTGGTGCAGGAGGGGGACACGTACTGGTACATGATGACCACGAAGAGGAGA AGTTGGTGCAGGAGCTGGTGCAGGAGGGGGACGCGTACTGGTACATGATGACCACGAAGAGGAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:96090888..96091008 26863196 MeRIP-seq:(Medium) rs1306326985 Functional Loss SNV dbSNP153 33..33 33 - - - 109239 RMVar_ID_109239 Human_SNP_ID_542030029 m1A Human chr13 + 97237964 97237964 97237964 GAGGCCAGGAGCAACTTACGAAGAGCATGGGCAGGATTGACTGGGGCCAAGGGAAAGGGAGGGAG GAGGCCAGGAGCAACTTACGAAGAGCATGGGCGGGATTGACTGGGGCCAAGGGAAAGGGAGGGAG A G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:97237875..97237988 26863196 MeRIP-seq:(Medium) rs997295450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6312694 RMVar_hsa_circ_100504,RMVar_hsa_circ_164231 109240 RMVar_ID_109240 Human_SNP_ID_542030182 m1A Human chr13 + 97238654 97238654 97238654 GTGCTGCGTGGGCTGCTGAACTGCAAGGCACCAGGGAAGTGGAAAGTGAAAACGATTAGGTAGGG GTGCTGCGTGGGCTGCTGAACTGCAAGGCACCGGGGAAGTGGAAAGTGAAAACGATTAGGTAGGG A G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:97238642..97238873 26863196 MeRIP-seq:(Medium) rs74571999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100504,RMVar_hsa_circ_164231 109241 RMVar_ID_109241 Human_SNP_ID_542042376 m1A Human chr13 + 97291120 97291120 97291120 CTGGAGGAGGGATGGTAGGAGGAGGAAGGGCCAGGTGGTTGGTTAAAAAAAGCCTCTGCATCACT CTGGAGGAGGGATGGTAGGAGGAGGAAGGGCCTGGTGGTTGGTTAAAAAAAGCCTCTGCATCACT A T MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:97291117..97291182 26863196 MeRIP-seq:(Medium) rs1165285980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97835,RMVar_hsa_circ_100504,RMVar_hsa_circ_120088,RMVar_hsa_circ_164231,RMVar_hsa_circ_110826,RMVar_hsa_circ_164234,RMVar_hsa_circ_164235,RMVar_hsa_circ_164233 109242 RMVar_ID_109242 Human_SNP_ID_542053352 m1A Human chr13 - 97339243 97339243 97339243 ACACACACAACACACTCATATACACAACACATACTCATACACATTCACAACACACTCCCATACAC ACACACACAACACACTCATATACACAACACATGCTCATACACATTCACAACACACTCCCATACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:97339128..97339367 26863196 MeRIP-seq:(Medium) rs1341134325 Functional Loss SNV dbSNP153 33..33 33 - - - 109243 RMVar_ID_109243 Human_SNP_ID_542059138 m1A Human chr13 - 97363402 97363402 97363402 CACACACACACACACAGTTTTTCTTTCTGGCAACTCCCTTTGTCTACTTTGCTGAACGATCTTCC CACACACACACACACAGTTTTTCTTTCTGGCATCTCCCTTTGTCTACTTTGCTGAACGATCTTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:97363389..97363536 26863196 MeRIP-seq:(Medium) rs1197666196 Functional Loss SNV dbSNP153 33..33 33 - - - 109244 RMVar_ID_109244 Human_SNP_ID_542209261 m1A Human chr13 - 97975971 97975971 97975971 ACGTACCTTCTACTCACGGACTTCTCGCTTTCAGACCCTCCGACCTCCCCCAGGGCTGTGGACTC ACGTACCTTCTACTCACGGACTTCTCGCTTTCGGACCCTCCGACCTCCCCCAGGGCTGTGGACTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:97975815..97976031 26863196 MeRIP-seq:(Medium) rs1036739888 Functional Loss SNV dbSNP153 33..33 33 - - - 109245 RMVar_ID_109245 Human_SNP_ID_542209572 m1A Human chr13 + 97976642 97976642 97976642 TGGGCCCGCCCCCGCCCCTCCCGCGGCCCGCGAGCGCGCCTCACGGCTCCTGTCTCCCCTCCCTC TGGGCCCGCCCCCGCCCCTCCCGCGGCCCGCGCGCGCGCCTCACGGCTCCTGTCTCCCCTCCCTC A C IPO5 Ensembl:ENSG00000065150 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr13:97976540..97976700 26863410 MeRIP-seq:(Medium) rs751597657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276492,Human_RBP_ID_18936441 RMVar_hsa_circ_113948,RMVar_hsa_circ_89995,RMVar_hsa_circ_164257,RMVar_hsa_circ_164258 109246 RMVar_ID_109246 Human_SNP_ID_542209656 m1A Human chr13 - 97976788 97976788 97976788 AGGGCGCGAAGACTGGGGCGGCGAACTCGGTTACCTCTGCCTGTTTCCGGACCACATTGTCGGGG AGGGCGCGAAGACTGGGGCGGCGAACTCGGTTGCCTCTGCCTGTTTCCGGACCACATTGTCGGGG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:97976759..97976877 26863196 MeRIP-seq:(Medium) rs1421278681 Functional Loss SNV dbSNP153 33..33 33 - - - 109247 RMVar_ID_109247 Human_SNP_ID_542211256 m1A Human chr13 - 97982449 97982449 97982449 GTTAGGAAAGAATGTTAGGAAACTTCATGAGTAAACCAGTGAAAGAAATAAACAGTGGGAAGGAT GTTAGGAAAGAATGTTAGGAAACTTCATGAGTGAACCAGTGAAAGAAATAAACAGTGGGAAGGAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:97982443..97982527 26863196 MeRIP-seq:(Medium) rs1053397843 Functional Loss SNV dbSNP153 33..33 33 - - - 109248 RMVar_ID_109248 Human_SNP_ID_542219136 m1A Human chr13 + 98010217 98010217 98010217 TGCAGGACTAGAAGAAAAATCAACTGCTTGCCAGATGTTGGTAAGAGAGCACTGTTTTTACTAAA TGCAGGACTAGAAGAAAAATCAACTGCTTGCCGGATGTTGGTAAGAGAGCACTGTTTTTACTAAA A G IPO5 Ensembl:ENSG00000065150 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1437805996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_195971,Human_RBP_ID_880088,Human_RBP_ID_1486963,Human_RBP_ID_1813849,Human_RBP_ID_3944318,Human_RBP_ID_9367680,Human_RBP_ID_17843848,Human_RBP_ID_19062939 Human_Splice_Rec_1476283,Human_Splice_Rec_1476337,Human_Splice_Rec_1476485,Human_Splice_Rec_1476557,Human_Splice_Rec_1476621,Human_Splice_Rec_1476661 RMVar_hsa_circ_796,RMVar_hsa_circ_113948,RMVar_hsa_circ_89995,RMVar_hsa_circ_164257,RMVar_hsa_circ_164258,RMVar_hsa_circ_372651,RMVar_hsa_circ_86408,RMVar_hsa_circ_164262,RMVar_hsa_circ_91206,RMVar_hsa_circ_164263,RMVar_hsa_circ_107629,RMVar_hsa_circ_164265,RMVar_hsa_circ_50849,RMVar_hsa_circ_39029,RMVar_hsa_circ_371626,RMVar_hsa_circ_164268,RMVar_hsa_circ_300223,RMVar_hsa_circ_164272,RMVar_hsa_circ_85886,RMVar_hsa_circ_12219,RMVar_hsa_circ_164275,RMVar_hsa_circ_12468,RMVar_hsa_circ_1816,RMVar_hsa_circ_373663,RMVar_hsa_circ_164276,RMVar_hsa_circ_358262,RMVar_hsa_circ_164280,RMVar_hsa_circ_101075,RMVar_hsa_circ_267030,RMVar_hsa_circ_95361,RMVar_hsa_circ_164281,RMVar_hsa_circ_164282 109249 RMVar_ID_109249 Human_SNP_ID_542222177 m1A Human chr13 + 98021788 98021788 98021788 TGAGTGCATAGCACAGCTCAGTCCTGAGCAGCAGGCCGCCATTCAGGAGCTCCTGAACTCTGCGT TGAGTGCATAGCACAGCTCAGTCCTGAGCAGCGGGCCGCCATTCAGGAGCTCCTGAACTCTGCGT A G IPO5 Ensembl:ENSG00000065150 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:98021726..98022104 32194978 MeRIP-seq:(Medium) rs1251985525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230555,Human_RBP_ID_1813884,Human_RBP_ID_4275975,Human_RBP_ID_17246117,Human_RBP_ID_22757617 Human_Splice_Rec_1476298,Human_Splice_Rec_1476352,Human_Splice_Rec_1476500,Human_Splice_Rec_1476572,Human_Splice_Rec_1476636,Human_Splice_Rec_1476676 109250 RMVar_ID_109250 Human_SNP_ID_542252294 m1A Human chr13 + 98143248 98143248 98143248 CGAGTAGCGCTGGCCCCGGCGTCGAGGCGGCCATGGCGACCCGGAGCCCGCTCCCCACCCACCCC CGAGTAGCGCTGGCCCCGGCGTCGAGGCGGCCCTGGCGACCCGGAGCCCGCTCCCCACCCACCCC A C FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:98143134..98143258 26863196 MeRIP-seq:(Medium) rs1339709724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276493 109251 RMVar_ID_109251 Human_SNP_ID_542252295 m1A Human chr13 + 98143248 98143248 98143248 CGAGTAGCGCTGGCCCCGGCGTCGAGGCGGCCATGGCGACCCGGAGCCCGCTCCCCACCCACCCC CGAGTAGCGCTGGCCCCGGCGTCGAGGCGGCCTTGGCGACCCGGAGCCCGCTCCCCACCCACCCC A T FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:98143134..98143258 26863196 MeRIP-seq:(Medium) rs1339709724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276493 109252 RMVar_ID_109252 Human_SNP_ID_542299885 m1A Human chr13 + 98330079 98330079 98330079 TGACGTGAGCAAAGCGAAGAAAGAGGTGAGGGAATTAGCCACAAAGATTTCTGGGGACAGAGTGT TGACGTGAGCAAAGCGAAGAAAGAGGTGAGGGGATTAGCCACAAAGATTTCTGGGGACAGAGTGT A G FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:98330075..98330204 26863196 MeRIP-seq:(Medium) rs922086603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164287,RMVar_hsa_circ_54973,RMVar_hsa_circ_282225,RMVar_hsa_circ_321225,RMVar_hsa_circ_312229,RMVar_hsa_circ_112161,RMVar_hsa_circ_82445,RMVar_hsa_circ_164289,RMVar_hsa_circ_36662,RMVar_hsa_circ_164290,RMVar_hsa_circ_164288,RMVar_hsa_circ_21852 109253 RMVar_ID_109253 Human_SNP_ID_542309638 m1A Human chr13 + 98370271 98370271 98370271 GAATCAGCTCCAAGCATTCAAATACATAAAGGAGGGCCAGCATGGCAGGAGTGTTGGGAGCGTCG GAATCAGCTCCAAGCATTCAAATACATAAAGGTGGGCCAGCATGGCAGGAGTGTTGGGAGCGTCG A T FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:98370270..98370447 26863196 MeRIP-seq:(Medium) rs1236108111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164287,RMVar_hsa_circ_54973,RMVar_hsa_circ_282225,RMVar_hsa_circ_112161,RMVar_hsa_circ_82445,RMVar_hsa_circ_164289,RMVar_hsa_circ_36662,RMVar_hsa_circ_164288,RMVar_hsa_circ_71159,RMVar_hsa_circ_351099,RMVar_hsa_circ_328962,RMVar_hsa_circ_73722,RMVar_hsa_circ_78761,RMVar_hsa_circ_72738,RMVar_hsa_circ_23388,RMVar_hsa_circ_164301,RMVar_hsa_circ_286484,RMVar_hsa_circ_267581,RMVar_hsa_circ_39169,RMVar_hsa_circ_164302,RMVar_hsa_circ_363921,RMVar_hsa_circ_164304 109254 RMVar_ID_109254 Human_SNP_ID_542316571 m1A Human chr13 - 98395346 98395346 98395346 TGCTTGTTACCCGCGGGGCTTCTCCTCGGCGCAGGGCTCGGGTGCGACCCCGGCTCCCCGGCGGA TGCTTGTTACCCGCGGGGCTTCTCCTCGGCGCGGGGCTCGGGTGCGACCCCGGCTCCCCGGCGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:98395298..98395523 26863196 MeRIP-seq:(Medium) rs759018309 Functional Loss SNV dbSNP153 33..33 33 - - - 109255 RMVar_ID_109255 Human_SNP_ID_542318413 m1A Human chr13 + 98402211 98402211 98402211 GTGCTGCTGGGGCCAGGTGCAGCAATTGCAGAATGTTGAGGAGTGAGGAGTAGTTAGAAATCACT GTGCTGCTGGGGCCAGGTGCAGCAATTGCAGAGTGTTGAGGAGTGAGGAGTAGTTAGAAATCACT A G FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:98402195..98402393 26863196 MeRIP-seq:(Medium) rs1002466630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17115243 RMVar_hsa_circ_164287,RMVar_hsa_circ_82445,RMVar_hsa_circ_36662,RMVar_hsa_circ_71159,RMVar_hsa_circ_351099,RMVar_hsa_circ_78761,RMVar_hsa_circ_164301,RMVar_hsa_circ_267581,RMVar_hsa_circ_39169,RMVar_hsa_circ_40368,RMVar_hsa_circ_359184,RMVar_hsa_circ_277511,RMVar_hsa_circ_31541,RMVar_hsa_circ_164310,RMVar_hsa_circ_266372,RMVar_hsa_circ_267464,RMVar_hsa_circ_267028,RMVar_hsa_circ_62436,RMVar_hsa_circ_107526,RMVar_hsa_circ_164313,RMVar_hsa_circ_55332,RMVar_hsa_circ_164314,RMVar_hsa_circ_90573 109256 RMVar_ID_109256 Human_SNP_ID_542318418 m1A Human chr13 - 98402243 98402243 98402243 GCGTCCTTGGTCTGTGTGCTTTTCCATGTTGCAGTGATTTCTAACTACTCCTCACTCCTCAACAT GCGTCCTTGGTCTGTGTGCTTTTCCATGTTGCGGTGATTTCTAACTACTCCTCACTCCTCAACAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:98402234..98402387 26863196 MeRIP-seq:(Medium) rs1184688607 Functional Loss SNV dbSNP153 33..33 33 - - - 109257 RMVar_ID_109257 Human_SNP_ID_542322298 m1A Human chr13 + 98417551 98417551 98417551 GGTCTTGGAGAATGGCAGCCAGGAGGGCAAGGATGGTTTGAGGAAGGTAGTTCCTGGTGTACAGG GGTCTTGGAGAATGGCAGCCAGGAGGGCAAGGTTGGTTTGAGGAAGGTAGTTCCTGGTGTACAGG A T FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:98417547..98417632 26863196 MeRIP-seq:(Medium) rs866817628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6900,RMVar_hsa_circ_36662,RMVar_hsa_circ_71159,RMVar_hsa_circ_78761,RMVar_hsa_circ_164301,RMVar_hsa_circ_267581,RMVar_hsa_circ_39169,RMVar_hsa_circ_359184,RMVar_hsa_circ_31541,RMVar_hsa_circ_266372,RMVar_hsa_circ_267464,RMVar_hsa_circ_267028,RMVar_hsa_circ_62436,RMVar_hsa_circ_55332,RMVar_hsa_circ_69749,RMVar_hsa_circ_290567,RMVar_hsa_circ_164314,RMVar_hsa_circ_90573,RMVar_hsa_circ_333272,RMVar_hsa_circ_95882,RMVar_hsa_circ_75831,RMVar_hsa_circ_164317,RMVar_hsa_circ_164319,RMVar_hsa_circ_164321,RMVar_hsa_circ_36912,RMVar_hsa_circ_164320,RMVar_hsa_circ_164318,RMVar_hsa_circ_164322 109258 RMVar_ID_109258 Human_SNP_ID_542354850 m1A Human chr13 + 98536816 98536816 98536816 CACTCAACAGAACCAGAAACACATACCCTGCCAGCCACCACACTCCTCCGCCTGTCCTCCAGCTG CACTCAACAGAACCAGAAACACATACCCTGCCGGCCACCACACTCCTCCGCCTGTCCTCCAGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:98536813..98536951 26863196 MeRIP-seq:(Medium) rs1457428990 Functional Loss SNV dbSNP153 33..33 33 - - - 109259 RMVar_ID_109259 Human_SNP_ID_542365494 m1A Human chr13 + 98576803 98576803 98576803 CCGGGGAGTGAGCCATGGCGCTCAGGACGGCCACTTCCTGGGACGGGACGGCCGGGCCGCGACGA CCGGGGAGTGAGCCATGGCGCTCAGGACGGCCGCTTCCTGGGACGGGACGGCCGGGCCGCGACGA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr13:98576726..98577100;chr13:98576726..98576875 26863196 MeRIP-seq:(Medium) rs1161445922 Functional Loss SNV dbSNP153 33..33 33 - - - 109260 RMVar_ID_109260 Human_SNP_ID_542365498 m1A Human chr13 - 98576809 98576809 98576809 CGCGGATCGTCGCGGCCCGGCCGTCCCGTCCCAGGAAGTGGCCGTCCTGAGCGCCATGGCTCACT CGCGGATCGTCGCGGCCCGGCCGTCCCGTCCCGGGAAGTGGCCGTCCTGAGCGCCATGGCTCACT T C STK24 Ensembl:ENSG00000102572 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:98576751..98577133 26863196 MeRIP-seq:(Medium) rs1375964998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276272,Human_RBP_ID_5493088,Human_RBP_ID_8792023 Human_Splice_Rec_1477083,Human_Splice_Rec_1477103 109261 RMVar_ID_109261 Human_SNP_ID_542365578 m1A Human chr13 - 98577024 98577024 98577024 CCAGCAGTAGCGGCAGCAGCGGCGGCGGCGGCAGTGCGCGCGAGGCCCTGCGCCCCCAGCAGCTC CCAGCAGTAGCGGCAGCAGCGGCGGCGGCGGCGGTGCGCGCGAGGCCCTGCGCCCCCAGCAGCTC T C STK24 Ensembl:ENSG00000102572 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr13:98576982..98577133 26863410 MeRIP-seq:(Medium) rs1044591626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276285,Human_RBP_ID_9368062 109262 RMVar_ID_109262 Human_SNP_ID_542365596 m1A Human chr13 - 98577051 98577051 98577051 CGCGGGCCCAGGCCGCCCGGCTCCAGCCCAGCAGTAGCGGCAGCAGCGGCGGCGGCGGCAGTGCG CGCGGGCCCAGGCCGCCCGGCTCCAGCCCAGCGGTAGCGGCAGCAGCGGCGGCGGCGGCAGTGCG T C STK24 Ensembl:ENSG00000102572 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:98576801..98577100;chr13:98576823..98577100 26863196 MeRIP-seq:(Medium) rs1371401172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4276496,Human_RBP_ID_9368062 109263 RMVar_ID_109263 Human_SNP_ID_542485285 m1A Human chr13 - 99073227 99073227 99073227 GATTTTCTATTAGGCAAAGCATGGGAATTGACATCAGGGGTAGGATATGCAGGGTGGGCTGGGCA GATTTTCTATTAGGCAAAGCATGGGAATTGACTTCAGGGGTAGGATATGCAGGGTGGGCTGGGCA T A DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99073224..99073478 26863196 MeRIP-seq:(Medium) rs1474867431 Functional Loss SNV dbSNP153 33..33 33 - - - 109264 RMVar_ID_109264 Human_SNP_ID_542485325 m1A Human chr13 - 99073349 99073346 99073349 GAGAGAGAGAGGAGAGAGAGAAAAGAAGAAGAAGAGAGGAGAGAAAGAAGAGAGAGAAGAGAGAG GAGAGAGAGAGGAGAGAGAGAAAAGAAGAAGA___GAGGAGAGAAAGAAGAGAGAGAAGAGAGAG CTCT C DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:99073342..99073426 26863196 MeRIP-seq:(Medium) rs765715965 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_25081387 109265 RMVar_ID_109265 Human_SNP_ID_542488697 m1A Human chr13 - 99086615 99086615 99086615 GGTGGCATGGGGGAGCCGCCGCCGCCACACGCACGGTCGCCCGGAGCGAGCCCGGGCGCTGCTGC GGTGGCATGGGGGAGCCGCCGCCGCCACACGCGCGGTCGCCCGGAGCGAGCCCGGGCGCTGCTGC T C DOCK9 Ensembl:ENSG00000088387 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:99086354..99086650 26863196 MeRIP-seq:(Medium) rs1262362908 Functional Loss SNV dbSNP153 33..33 33 - - - 109266 RMVar_ID_109266 Human_SNP_ID_542488699 m1A Human chr13 + 99086640 99086621 99086640 GCGACCGTGCGTGTGGCGGCGGCGGCTCCCCCATGCCACCAGCCTCCCTCGGCGACCACTCGCCG GCGACCGTGCGTGT___________________TGCCACCAGCCTCCCTCGGCGACCACTCGCCG TGGCGGCGGCGGCTCCCCCA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99086242..99086675 26863196 MeRIP-seq:(Medium) rs1322637741 Functional Loss DEL dbSNP153 15..33 33 - - - 109267 RMVar_ID_109267 Human_SNP_ID_542488710 m1A Human chr13 + 99086640 99086640 99086640 GCGACCGTGCGTGTGGCGGCGGCGGCTCCCCCATGCCACCAGCCTCCCTCGGCGACCACTCGCCG GCGACCGTGCGTGTGGCGGCGGCGGCTCCCCCGTGCCACCAGCCTCCCTCGGCGACCACTCGCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99086242..99086675 26863196 MeRIP-seq:(Medium) rs1178973474 Functional Loss SNV dbSNP153 33..33 33 - - - 109268 RMVar_ID_109268 Human_SNP_ID_542519331 m1A Human chr13 + 99206114 99206114 99206114 ACTAGAGAGGGAATGCAGAGAAGCAGGAGCTCATTTCAGGAGAAGATGAGTTCAGCTTTGGACCT ACTAGAGAGGGAATGCAGAGAAGCAGGAGCTCGTTTCAGGAGAAGATGAGTTCAGCTTTGGACCT A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99206102..99206297 26863196 MeRIP-seq:(Medium) rs928534950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6314098,Human_RBP_ID_12252100 RMVar_hsa_circ_24041,RMVar_hsa_circ_82397,RMVar_hsa_circ_323112,RMVar_hsa_circ_164376,RMVar_hsa_circ_331666,RMVar_hsa_circ_61741 109269 RMVar_ID_109269 Human_SNP_ID_542519337 m1A Human chr13 + 99206135 99206135 99206135 AGCAGGAGCTCATTTCAGGAGAAGATGAGTTCAGCTTTGGACCTGTGCAGTGTTGAGGGGTTTGC AGCAGGAGCTCATTTCAGGAGAAGATGAGTTCGGCTTTGGACCTGTGCAGTGTTGAGGGGTTTGC A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99206133..99206264 26863196 MeRIP-seq:(Medium) rs980299265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12252100 RMVar_hsa_circ_24041,RMVar_hsa_circ_82397,RMVar_hsa_circ_323112,RMVar_hsa_circ_164376,RMVar_hsa_circ_331666,RMVar_hsa_circ_61741 109270 RMVar_ID_109270 Human_SNP_ID_542555308 m1A Human chr13 + 99349475 99349475 99349475 GGGCCCGAGGGACCACTGCCATCAAGATGCGGAGACCAGTAGTGGCCCTGAACGGCTGGGTGCGC GGGCCCGAGGGACCACTGCCATCAAGATGCGGGGACCAGTAGTGGCCCTGAACGGCTGGGTGCGC A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99349470..99349573 26863196 MeRIP-seq:(Medium) rs1252204696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71441,RMVar_hsa_circ_297324,RMVar_hsa_circ_164384,RMVar_hsa_circ_296145,RMVar_hsa_circ_34544,RMVar_hsa_circ_164385 109271 RMVar_ID_109271 Human_SNP_ID_542557502 m1A Human chr13 - 99358012 99358012 99358012 ATTTCACTTGCAGGCTAACCGGCCTGAATCTCACAACAGCCTATTAGCTCCACGGGGACTGTGAT ATTTCACTTGCAGGCTAACCGGCCTGAATCTCCCAACAGCCTATTAGCTCCACGGGGACTGTGAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99358010..99358177 26863196 MeRIP-seq:(Medium) rs1353272381 Functional Loss SNV dbSNP153 33..33 33 - - - 109272 RMVar_ID_109272 Human_SNP_ID_542561259 m1A Human chr13 - 99373559 99373559 99373559 TCTTTGTCCACCTGTTTCCCTGCCCTGGGCTCACAGCTCCTCAGGGCAGGACATTCCGCCTTATC TCTTTGTCCACCTGTTTCCCTGCCCTGGGCTCGCAGCTCCTCAGGGCAGGACATTCCGCCTTATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99373551..99373806 26863196 MeRIP-seq:(Medium) rs993943022 Functional Loss SNV dbSNP153 33..33 33 - - - 109273 RMVar_ID_109273 Human_SNP_ID_542562117 m1A Human chr13 - 99376988 99376979 99376989 GGCGTGAGTGGAGGCAATGGTGAGGCGAGGCGAGGCGAGGCACGGCGCTGCATACTGCAACTTCG GGCGTGAGTGGAGGCAATGGTGAGGCGAGGC__________ACGGCGCTGCATACTGCAACTTCG TGCCTCGCCTC T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99376981..99377054 26863196 MeRIP-seq:(Medium) rs151322129 Functional Loss DEL dbSNP153 32..41 33 - - - 109274 RMVar_ID_109274 Human_SNP_ID_542562118 m1A Human chr13 - 99376988 99376979 99376989 GGCGTGAGTGGAGGCAATGGTGAGGCGAGGCGAGGCGAGGCACGGCGCTGCATACTGCAACTTCG GGCGTGAGTGGAGGCAATGGTGAGGCGAGGC_____GAGGCACGGCGCTGCATACTGCAACTTCG TGCCTCGCCTC TGCCTC - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99376981..99377054 26863196 MeRIP-seq:(Medium) rs151322129 Functional Loss DEL dbSNP153 32..36 33 - - - 109275 RMVar_ID_109275 Human_SNP_ID_542563484 m1A Human chr13 - 99382761 99382761 99382761 TTTCCATGTCTCCCAGACTAGAAGGCCCCCAGAGCGAAGTCCTCATTGCCCCACTGCCTTCTGTC TTTCCATGTCTCCCAGACTAGAAGGCCCCCAGCGCGAAGTCCTCATTGCCCCACTGCCTTCTGTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99382754..99382961 26863196 MeRIP-seq:(Medium) rs1483272583 Functional Loss SNV dbSNP153 33..33 33 - - - 109276 RMVar_ID_109276 Human_SNP_ID_542564225 m1A Human chr13 + 99385349 99385349 99385349 CTTCCTGCTGCAGCACTGATAGTCCCAGGCCAACACTGGGACCGGACCGGCAGCCGAGTGACAGT CTTCCTGCTGCAGCACTGATAGTCCCAGGCCAGCACTGGGACCGGACCGGCAGCCGAGTGACAGT A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs750048232 Functional Loss SNV dbSNP153 33..33 33 - - - 109277 RMVar_ID_109277 Human_SNP_ID_542564395 m1A Human chr13 + 99385889 99385889 99385889 AGGCCAGAGGACTCTGCAGTACCTTCTCCTACATCTAGTAACAAAGAATGGTGATAACCATGCAC AGGCCAGAGGACTCTGCAGTACCTTCTCCTACCTCTAGTAACAAAGAATGGTGATAACCATGCAC A C UBAC2 Ensembl:ENSG00000134882 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:99385839..99385939 32194978 MeRIP-seq:(Medium) rs757832596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275837,Human_RBP_ID_431415,Human_RBP_ID_1480392,Human_RBP_ID_4261091,Human_RBP_ID_8386409,Human_RBP_ID_9280086,Human_RBP_ID_17243815,Human_RBP_ID_17358801,Human_RBP_ID_17475317,Human_RBP_ID_17832707,Human_RBP_ID_18266063,Human_RBP_ID_27635703 109278 RMVar_ID_109278 Human_SNP_ID_542564396 m1A Human chr13 + 99385889 99385889 99385889 AGGCCAGAGGACTCTGCAGTACCTTCTCCTACATCTAGTAACAAAGAATGGTGATAACCATGCAC AGGCCAGAGGACTCTGCAGTACCTTCTCCTACGTCTAGTAACAAAGAATGGTGATAACCATGCAC A G UBAC2 Ensembl:ENSG00000134882 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:99385839..99385939 32194978 MeRIP-seq:(Medium) rs757832596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_275837,Human_RBP_ID_431415,Human_RBP_ID_1480392,Human_RBP_ID_4261091,Human_RBP_ID_8386409,Human_RBP_ID_9280086,Human_RBP_ID_17243815,Human_RBP_ID_17358801,Human_RBP_ID_17475317,Human_RBP_ID_17832707,Human_RBP_ID_18266063,Human_RBP_ID_27635703 109279 RMVar_ID_109279 Human_SNP_ID_542595941 m1A Human chr13 + 99501601 99501601 99501601 CCCCTAGGTTTGATTGCCCTTTCCCCGAAACAACTATCATGAGCGCGAGGCTGCCGGTGTTGTCT CCCCTAGGTTTGATTGCCCTTTCCCCGAAACACCTATCATGAGCGCGAGGCTGCCGGTGTTGTCT A C TM9SF2 Ensembl:ENSG00000125304 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:99501551..99501625 26863196 MeRIP-seq:(Medium) rs1287088373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431430,Human_RBP_ID_4276672,Human_RBP_ID_5438268,Human_RBP_ID_5463072,Human_RBP_ID_6253013,Human_RBP_ID_9323529,Human_RBP_ID_17832720,Human_RBP_ID_18635710,Human_RBP_ID_18936471,Human_RBP_ID_22438218,Human_RBP_ID_26807563,Human_RBP_ID_26913122,Human_RBP_ID_27219427,Human_RBP_ID_27635704 109280 RMVar_ID_109280 Human_SNP_ID_542602097 m1A Human chr13 + 99526463 99526463 99526463 TTGAGCTTGCACAGGGGGCATGTGAGGCCACAAAAGGAGTAAGAGACAGTGAAAAGACTGTAGGA TTGAGCTTGCACAGGGGGCATGTGAGGCCACAGAAGGAGTAAGAGACAGTGAAAAGACTGTAGGA A G TM9SF2 Ensembl:ENSG00000125304 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99526458..99526913 26863196 MeRIP-seq:(Medium) rs1566566439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_812329,Human_RBP_ID_12090614 RMVar_hsa_circ_813,RMVar_hsa_circ_127100,RMVar_hsa_circ_369905,RMVar_hsa_circ_351470,RMVar_hsa_circ_44146,RMVar_hsa_circ_96561,RMVar_hsa_circ_121233,RMVar_hsa_circ_91100,RMVar_hsa_circ_128127,RMVar_hsa_circ_164387,RMVar_hsa_circ_164389,RMVar_hsa_circ_164390,RMVar_hsa_circ_164388,RMVar_hsa_circ_335656,RMVar_hsa_circ_164386,RMVar_hsa_circ_309758,RMVar_hsa_circ_81449,RMVar_hsa_circ_85023,RMVar_hsa_circ_26569,RMVar_hsa_circ_164392,RMVar_hsa_circ_164394,RMVar_hsa_circ_164395,RMVar_hsa_circ_164393,RMVar_hsa_circ_164391 109281 RMVar_ID_109281 Human_SNP_ID_542607771 m1A Human chr13 - 99549175 99549175 99549175 GATGTTAATAAAACATTTGTTTTCCACTTCTCACCTCCAAAGGCTATAGAAGAAAACAAAAGTTG GATGTTAATAAAACATTTGTTTTCCACTTCTCCCCTCCAAAGGCTATAGAAGAAAACAAAAGTTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:99549151..99549225 32194978 MeRIP-seq:(Medium) rs757463078 Functional Loss SNV dbSNP153 33..33 33 - - - 109282 RMVar_ID_109282 Human_SNP_ID_542622162 m1A Human chr13 + 99606731 99606709 99606731 GCGCTACGTCTGCTGCGGAGGGCGGCGCGCGGAGCTGCGGCGGCGGCGCTGCTGAGGCTGTGAGT GCGCTACGTCT______________________GCTGCGGCGGCGGCGCTGCTGAGGCTGTGAGT TGCTGCGGAGGGCGGCGCGCGGA T CLYBL Ensembl:ENSG00000125246 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99606681..99606778 26863196 MeRIP-seq:(Medium) rs1298925428 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_18417743 Human_Splice_Rec_1478411,Human_Splice_Rec_1478425,Human_Splice_Rec_1478437 109283 RMVar_ID_109283 Human_SNP_ID_542622189 m1A Human chr13 + 99606731 99606731 99606731 GCGCTACGTCTGCTGCGGAGGGCGGCGCGCGGAGCTGCGGCGGCGGCGCTGCTGAGGCTGTGAGT GCGCTACGTCTGCTGCGGAGGGCGGCGCGCGGGGCTGCGGCGGCGGCGCTGCTGAGGCTGTGAGT A G CLYBL Ensembl:ENSG00000125246 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99606681..99606778 26863196 MeRIP-seq:(Medium) rs371782189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18417743 Human_Splice_Rec_1478411,Human_Splice_Rec_1478425,Human_Splice_Rec_1478437 109284 RMVar_ID_109284 Human_SNP_ID_542622195 m1A Human chr13 - 99606734 99606734 99606734 TGCACTCACAGCCTCAGCAGCGCCGCCGCCGCAGCTCCGCGCGCCGCCCTCCGCAGCAGACGTAG TGCACTCACAGCCTCAGCAGCGCCGCCGCCGCGGCTCCGCGCGCCGCCCTCCGCAGCAGACGTAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:99606690..99606828;chr13:99606694..99606820 26863196 MeRIP-seq:(Medium) rs1352766554 Functional Loss SNV dbSNP153 33..33 33 - - - 109285 RMVar_ID_109285 Human_SNP_ID_542622196 m1A Human chr13 - 99606734 99606734 99606734 TGCACTCACAGCCTCAGCAGCGCCGCCGCCGCAGCTCCGCGCGCCGCCCTCCGCAGCAGACGTAG TGCACTCACAGCCTCAGCAGCGCCGCCGCCGCCGCTCCGCGCGCCGCCCTCCGCAGCAGACGTAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:99606690..99606828;chr13:99606694..99606820 26863196 MeRIP-seq:(Medium) rs1352766554 Functional Loss SNV dbSNP153 33..33 33 - - - 109286 RMVar_ID_109286 Human_SNP_ID_542633612 m1A Human chr13 - 99653092 99653090 99653092 CCTTCAGATTGGCTTGTCTTTTCCCAACAAACAGTATACATTCCTGCCTCCTGTGATTTTCCTCA CCTTCAGATTGGCTTGTCTTTTCCCAACAAAC__TATACATTCCTGCCTCCTGTGATTTTCCTCA ACT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99653090..99653185 26863196 MeRIP-seq:(Medium) rs970695449 Functional Loss DEL dbSNP153 33..34 33 - - - 109287 RMVar_ID_109287 Human_SNP_ID_542638849 m1A Human chr13 + 99674478 99674478 99674478 AGCTGATAGCTACTAGAATTCTAAGTGGAGGTATGAAGTAGGCAGTTTTGGGGAGAGAGGCTGGG AGCTGATAGCTACTAGAATTCTAAGTGGAGGTGTGAAGTAGGCAGTTTTGGGGAGAGAGGCTGGG A G CLYBL Ensembl:ENSG00000125246 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99674476..99674582 26863196 MeRIP-seq:(Medium) rs1476483112 Functional Loss SNV dbSNP153 33..33 33 - - - 109288 RMVar_ID_109288 Human_SNP_ID_542712773 m1A Human chr13 + 99970080 99970080 99970080 AGGAGAAGCAGCGGCGGAAGCGGCGGCGGCGCAGGAGCTGGTGGCGGCGGCGGCGGCGCGGCCGG AGGAGAAGCAGCGGCGGAAGCGGCGGCGGCGCTGGAGCTGGTGGCGGCGGCGGCGGCGCGGCCGG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99970031..99970154 26863196 MeRIP-seq:(Medium) rs755369378 Functional Loss SNV dbSNP153 33..33 33 - - - 109289 RMVar_ID_109289 Human_SNP_ID_542712850 m1A Human chr13 - 99970273 99970273 99970273 CCACGTCTGCTTCTGGGAGGACTGTCCGCGCGAGGGCAAGCCCTTCAAGGCCAAATACAAGCTCA CCACGTCTGCTTCTGGGAGGACTGTCCGCGCGCGGGCAAGCCCTTCAAGGCCAAATACAAGCTCA T G ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99970227..99970666 26863196 MeRIP-seq:(Medium) rs768410616 Functional Loss SNV dbSNP153 33..33 33 - - - 109290 RMVar_ID_109290 Human_SNP_ID_542712915 m1A Human chr13 - 99970413 99970407 99970413 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC______CCCGGCCGGCGGCGCCAAGCCCTGCTC GGGCGGT G ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr13:99970312..99970662;chr13:99970149..99970440;chr13:99970382..99970495;chr13:99970253..99971161 26863196 MeRIP-seq:(Medium) rs1555331221 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_4261301 109291 RMVar_ID_109291 Human_SNP_ID_542712920 m1A Human chr13 - 99970413 99970410 99970413 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC___GCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CGGT C ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr13:99970312..99970662;chr13:99970149..99970440;chr13:99970382..99970495;chr13:99970253..99971161 26863196 MeRIP-seq:(Medium) rs1251453463 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_4261301 109292 RMVar_ID_109292 Human_SNP_ID_542712941 m1A Human chr13 - 99970413 99970413 99970413 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC T C ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr13:99970312..99970662;chr13:99970149..99970440;chr13:99970382..99970495;chr13:99970253..99971161 26863196 MeRIP-seq:(Medium) rs1357567471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4261301 109293 RMVar_ID_109293 Human_SNP_ID_542712942 m1A Human chr13 - 99970413 99970413 99970413 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC T G ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr13:99970312..99970662;chr13:99970149..99970440;chr13:99970382..99970495;chr13:99970253..99971161 26863196 MeRIP-seq:(Medium) rs1357567471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4261301 109294 RMVar_ID_109294 Human_SNP_ID_542713043 m1A Human chr13 - 99970555 99970555 99970555 GCCGGCGCCCGCGCAGCACCCGCACCAGCACCACCCCCACCTCCCAGGGGCGGCTGGGGCCTTCC GCCGGCGCCCGCGCAGCACCCGCACCAGCACCTCCCCCACCTCCCAGGGGCGGCTGGGGCCTTCC T A ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:99970462..99970562 26863410 MeRIP-seq:(Medium) rs1202236780 Functional Loss SNV dbSNP153 33..33 33 - - - 109295 RMVar_ID_109295 Human_SNP_ID_542713265 m1A Human chr13 + 99970951 99970951 99970951 CGTCCGGGCCCGCGTAGGTGCCGCTGGCGGAGATGAACATGCCGGCCGAGTGGGGAGGCGGGGCC CGTCCGGGCCCGCGTAGGTGCCGCTGGCGGAGGTGAACATGCCGGCCGAGTGGGGAGGCGGGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99970761..99971144 26863196 MeRIP-seq:(Medium) rs1241340716 Functional Loss SNV dbSNP153 33..33 33 - - - 109296 RMVar_ID_109296 Human_SNP_ID_542713524 m1A Human chr13 + 99971437 99971436 99971438 GCGGAGTGGTGGCCACGCCGGGGTCAGCGCCCAGGTCCCGCAGGCGGAGGTGCGCGACGGCGGCC GCGGAGTGGTGGCCACGCCGGGGTCAGCGCCC__GTCCCGCAGGCGGAGGTGCGCGACGGCGGCC CAG C HSALNG0098952 RNACentral:URS0000EB2DC2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99971210..99971560 26863196 MeRIP-seq:(Medium) rs1443588366 Functional Loss DEL dbSNP153 33..34 33 - - - 109297 RMVar_ID_109297 Human_SNP_ID_542713535 m1A Human chr13 + 99971452 99971452 99971452 CGCCGGGGTCAGCGCCCAGGTCCCGCAGGCGGAGGTGCGCGACGGCGGCCCGGAGTTGGGAGTGG CGCCGGGGTCAGCGCCCAGGTCCCGCAGGCGGGGGTGCGCGACGGCGGCCCGGAGTTGGGAGTGG A G HSALNG0098952 RNACentral:URS0000EB2DC2 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:99971229..99971612 26863196 MeRIP-seq:(Medium) rs1231385856 Functional Loss SNV dbSNP153 33..33 33 - - - 109298 RMVar_ID_109298 Human_SNP_ID_542716629 m1A Human chr13 + 99981747 99981747 99981747 CCTCCCCTGCCCTGCCCGCCCGCCCCCGCCGCAGCTCCTTTAATACACTTTGGTTCTCCGCCTGG CCTCCCCTGCCCTGCCCGCCCGCCCCCGCCGCCGCTCCTTTAATACACTTTGGTTCTCCGCCTGG A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:99981646..99981760 26863410 MeRIP-seq:(Medium) rs1373424345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431545,Human_RBP_ID_5438286,Human_RBP_ID_12092114,Human_RBP_ID_22040805,Human_RBP_ID_27219536 109299 RMVar_ID_109299 Human_SNP_ID_542716630 m1A Human chr13 + 99981747 99981747 99981747 CCTCCCCTGCCCTGCCCGCCCGCCCCCGCCGCAGCTCCTTTAATACACTTTGGTTCTCCGCCTGG CCTCCCCTGCCCTGCCCGCCCGCCCCCGCCGCTGCTCCTTTAATACACTTTGGTTCTCCGCCTGG A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr13:99981646..99981760 26863410 MeRIP-seq:(Medium) rs1373424345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431545,Human_RBP_ID_5438286,Human_RBP_ID_12092114,Human_RBP_ID_22040805,Human_RBP_ID_27219536 109300 RMVar_ID_109300 Human_SNP_ID_542716769 m1A Human chr13 - 99982082 99982082 99982082 AAGCTGCCCACCCCGATGGCCGGGAACTGCGGACCCGCGTCCAGGAGCATGGCCAGCGCGCCCGC AAGCTGCCCACCCCGATGGCCGGGAACTGCGGTCCCGCGTCCAGGAGCATGGCCAGCGCGCCCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:99981817..99982177;chr13:99981841..99982192 26863196 MeRIP-seq:(Medium) rs1276057222 Functional Loss SNV dbSNP153 33..33 33 - - - 109301 RMVar_ID_109301 Human_SNP_ID_542717174 m1A Human chr13 + 99983126 99983126 99983126 TTCGCGCGCTCCGAGAACCTCAAGATCCACAAAAGGACCCACACAGGTAACCGCGGGCTGGGACA TTCGCGCGCTCCGAGAACCTCAAGATCCACAATAGGACCCACACAGGTAACCGCGGGCTGGGACA A T ZIC2 Ensembl:ENSG00000043355 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:99982947..99983213 26863196 MeRIP-seq:(Medium) rs751358747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8386539,Human_RBP_ID_17832902 Human_Splice_Rec_1478505 109302 RMVar_ID_109302 Human_SNP_ID_542717991 m1A Human chr13 + 99985642 99985621 99985642 CTCTGGCGGGGGCAGCGGGACAGCCGGGGGTCACAGCGGCCTCTCCTCCAACTTCAATGAATGGT CTCTGGCGGGGG_____________________CAGCGGCCTCTCCTCCAACTTCAATGAATGGT GCAGCGGGACAGCCGGGGGTCA G ZIC2 Ensembl:ENSG00000043355 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:99985351..99985750 26863410 MeRIP-seq:(Medium) rs753845480 Functional Loss DEL dbSNP153 13..33 33 - - - Human_RBP_ID_6253644,Human_RBP_ID_17832909,Human_RBP_ID_23583161 Human_Splice_Rec_1478519 109303 RMVar_ID_109303 Human_SNP_ID_542718320 m1A Human chr13 + 99986526 99986526 99986526 TAAACGTCGTGCCGTTAGCTTTTTCCGTAATAACACCCTTCCTTCTGTAAATACCCGTTACCATA TAAACGTCGTGCCGTTAGCTTTTTCCGTAATAGCACCCTTCCTTCTGTAAATACCCGTTACCATA A G ZIC2 Ensembl:ENSG00000043355 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:99986385..99986550 26863196 MeRIP-seq:(Medium) rs561799594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431559,Human_RBP_ID_1480448,Human_RBP_ID_1804129,Human_RBP_ID_3422502,Human_RBP_ID_5438296,Human_RBP_ID_6253691,Human_RBP_ID_8072298,Human_RBP_ID_8386553,Human_RBP_ID_9025709,Human_RBP_ID_12092281,Human_RBP_ID_17243881,Human_RBP_ID_17358873,Human_RBP_ID_17475374,Human_RBP_ID_17832917,Human_RBP_ID_18266169,Human_RBP_ID_21885732,Human_RBP_ID_24468775,Human_RBP_ID_25076012,Human_RBP_ID_26424212,Human_RBP_ID_26616786,Human_RBP_ID_26913314,Human_RBP_ID_27219576,Human_RBP_ID_27426368,Human_RBP_ID_27635829 109304 RMVar_ID_109304 Human_SNP_ID_542745245 m1A Human chr13 - 100088846 100088846 100088846 CGGCCAGAGCCGACCCCAGGAGTGAGAGAGACAGGGGCGTGCGTGAGTTCCGGCGGCCTGCACCG CGGCCAGAGCCGACCCCAGGAGTGAGAGAGACTGGGGCGTGCGTGAGTTCCGGCGGCCTGCACCG T A PCCA-DT Ensembl:ENSG00000274605 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:100088655..100088925 26863196 MeRIP-seq:(Medium) rs755541253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4261522 109305 RMVar_ID_109305 Human_SNP_ID_542745246 m1A Human chr13 - 100088846 100088846 100088846 CGGCCAGAGCCGACCCCAGGAGTGAGAGAGACAGGGGCGTGCGTGAGTTCCGGCGGCCTGCACCG CGGCCAGAGCCGACCCCAGGAGTGAGAGAGACGGGGGCGTGCGTGAGTTCCGGCGGCCTGCACCG T C PCCA-DT Ensembl:ENSG00000274605 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:100088655..100088925 26863196 MeRIP-seq:(Medium) rs755541253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4261522 109306 RMVar_ID_109306 Human_SNP_ID_542745429 m1A Human chr13 + 100089165 100089165 100089165 TGGGTCGGGACAGCACCGCTGGTCGCTGCCGGACGGCGTGGGCGGTGGCCGCCGCAGCAGCTGAT TGGGTCGGGACAGCACCGCTGGTCGCTGCCGGGCGGCGTGGGCGGTGGCCGCCGCAGCAGCTGAT A G PCCA Ensembl:ENSG00000175198 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:100089114..100111852;chr13:100089115..100089223 26863196 MeRIP-seq:(Medium) rs1480725673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944330,Human_RBP_ID_4261538,Human_RBP_ID_18417744,Human_RBP_ID_18978659 Human_Splice_Rec_1478527,Human_Splice_Rec_1478571,Human_Splice_Rec_1478615,Human_Splice_Rec_1478661 109307 RMVar_ID_109307 Human_SNP_ID_542748747 m1A Human chr13 - 100102818 100102818 100102818 ATACTTGATGGGCTTTAGAACATTTTTTCAGGATATTTCTTCCAGTTAGGTTCTAGCGAACGTGT ATACTTGATGGGCTTTAGAACATTTTTTCAGGCTATTTCTTCCAGTTAGGTTCTAGCGAACGTGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:100102811..100102902 26863196 MeRIP-seq:(Medium) rs906197715 Functional Loss SNV dbSNP153 33..33 33 - - - 109308 RMVar_ID_109308 Human_SNP_ID_542841326 m1A Human chr13 + 100482417 100482417 100482417 TGAGGCAGGCTCCAAGAGAGGAGGGCAAAGCGAGATCAGGGGCTCCAGTGAAATGCCTGAGTGTG TGAGGCAGGCTCCAAGAGAGGAGGGCAAAGCGGGATCAGGGGCTCCAGTGAAATGCCTGAGTGTG A G PCCA Ensembl:ENSG00000175198 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:100482289..100482495 26863196 MeRIP-seq:(Medium) rs1455279360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355986,RMVar_hsa_circ_74000,RMVar_hsa_circ_272091,RMVar_hsa_circ_9701,RMVar_hsa_circ_124868,RMVar_hsa_circ_164483,RMVar_hsa_circ_54596,RMVar_hsa_circ_365019,RMVar_hsa_circ_350527 109309 RMVar_ID_109309 Human_SNP_ID_542851538 m1A Human chr13 - 100523513 100523513 100523513 CGAGTGTCACCCAGCATTGCTCTGTGCTGAAGAGCTGCAGACACCTCCAGCTGATGATGAATTGT CGAGTGTCACCCAGCATTGCTCTGTGCTGAAGGGCTGCAGACACCTCCAGCTGATGATGAATTGT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr13:100523485..100523572 26863410 MeRIP-seq:(Medium) rs1382043372 Functional Loss SNV dbSNP153 33..33 33 - - - 109310 RMVar_ID_109310 Human_SNP_ID_542877844 m1A Human chr13 + 100627613 100627613 100627613 TGTCTTAAAAGGACACCAGTCACACTGGATTAAGGGCCCACCATCCTCTTGTATGACCTCATCTT TGTCTTAAAAGGACACCAGTCACACTGGATTAGGGGCCCACCATCCTCTTGTATGACCTCATCTT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:100627459..100627626 26863196 MeRIP-seq:(Medium) rs1209818310 Functional Loss SNV dbSNP153 33..33 33 - - - 109311 RMVar_ID_109311 Human_SNP_ID_542890276 m1A Human chr13 - 100674740 100674740 100674740 GATGCGGCCGGGGCTCAGGCTCCTTGCAGGTAACGCGCGGGGCGGCCCCTGCAGGGCCGAGCGCG GATGCGGCCGGGGCTCAGGCTCCTTGCAGGTAGCGCGCGGGGCGGCCCCTGCAGGGCCGAGCGCG T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:100674731..100674889 26863196 MeRIP-seq:(Medium) rs1209647347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944152,Human_RBP_ID_4261634,Human_RBP_ID_19062271 109312 RMVar_ID_109312 Human_SNP_ID_543060962 m1A Human chr13 - 101360199 101360193 101360200 GGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGAAGAGAGGAAGAGAGGAAGAAA GGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA_______AGAGGAAGAGAGGAAGAGAGGAAGAAA TCTCTCTC T NALCN Ensembl:ENSG00000102452 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:101360149..101360302 26863196 MeRIP-seq:(Medium) rs1566614921 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_2707,RMVar_hsa_circ_47624,RMVar_hsa_circ_306554,RMVar_hsa_circ_317932,RMVar_hsa_circ_17785,RMVar_hsa_circ_266529,RMVar_hsa_circ_325864,RMVar_hsa_circ_300853,RMVar_hsa_circ_13603,RMVar_hsa_circ_348600,RMVar_hsa_circ_337542,RMVar_hsa_circ_52678,RMVar_hsa_circ_296876,RMVar_hsa_circ_316060,RMVar_hsa_circ_164517,RMVar_hsa_circ_164518,RMVar_hsa_circ_27673,RMVar_hsa_circ_272629,RMVar_hsa_circ_285058,RMVar_hsa_circ_53783,RMVar_hsa_circ_164519,RMVar_hsa_circ_278734,RMVar_hsa_circ_293815 109313 RMVar_ID_109313 Human_SNP_ID_543060974 m1A Human chr13 - 101360199 101360199 101360199 GGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGAAGAGAGGAAGAGAGGAAGAAA GGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGGAGAGAGAGGAAGAGAGGAAGAGAGGAAGAAA T C NALCN Ensembl:ENSG00000102452 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:101360149..101360302 26863196 MeRIP-seq:(Medium) rs991548640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2707,RMVar_hsa_circ_47624,RMVar_hsa_circ_306554,RMVar_hsa_circ_317932,RMVar_hsa_circ_17785,RMVar_hsa_circ_266529,RMVar_hsa_circ_325864,RMVar_hsa_circ_300853,RMVar_hsa_circ_13603,RMVar_hsa_circ_348600,RMVar_hsa_circ_337542,RMVar_hsa_circ_52678,RMVar_hsa_circ_296876,RMVar_hsa_circ_316060,RMVar_hsa_circ_164517,RMVar_hsa_circ_164518,RMVar_hsa_circ_27673,RMVar_hsa_circ_272629,RMVar_hsa_circ_285058,RMVar_hsa_circ_53783,RMVar_hsa_circ_164519,RMVar_hsa_circ_278734,RMVar_hsa_circ_293815 109314 RMVar_ID_109314 Human_SNP_ID_543074599 m1A Human chr13 - 101416432 101416432 101416432 AGCGCGCTGCCTGAGCTGAGCCGCCGTAGGTGAGGGGCCCGCGTCCCCGCCCGCCCTGGGCGCCG AGCGCGCTGCCTGAGCTGAGCCGCCGTAGGTGTGGGGCCCGCGTCCCCGCCCGCCCTGGGCGCCG T A NALCN Ensembl:ENSG00000102452 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:101416318..101416439 26863196 MeRIP-seq:(Medium) rs1566670676 Functional Loss SNV dbSNP153 33..33 33 - - - 109315 RMVar_ID_109315 Human_SNP_ID_543366728 m1A Human chr13 + 102597045 102597045 102597045 GCTTCCTCGTCCTCCATCCTGCGTCCATGGCCACCGCTGCGACTGAGGAGCCCTTCCCTTTTCAC GCTTCCTCGTCCTCCATCCTGCGTCCATGGCCGCCGCTGCGACTGAGGAGCCCTTCCCTTTTCAC A G TPP2 Ensembl:ENSG00000134900 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:102596995..102597145 26863196 MeRIP-seq:(Medium) rs770434482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8792024,Human_RBP_ID_9323667,Human_RBP_ID_23208449,Human_RBP_ID_26807570 109316 RMVar_ID_109316 Human_SNP_ID_543366731 m1A Human chr13 - 102597050 102597050 102597050 AGACCGTGAAAAGGGAAGGGCTCCTCAGTCGCAGCGGTGGCCATGGACGCAGGATGGAGGACGAG AGACCGTGAAAAGGGAAGGGCTCCTCAGTCGCTGCGGTGGCCATGGACGCAGGATGGAGGACGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr13:102596988..102597141;chr13:102597001..102597147;chr13:102596977..102597240 26863196 MeRIP-seq:(Medium) rs763497812 Functional Loss SNV dbSNP153 33..33 33 - - - 109317 RMVar_ID_109317 Human_SNP_ID_543368403 m1A Human chr13 - 102603528 102603528 102603528 CAAACTTTTTCCTGCCTCATGACTTTTTAAACAGGTTCCTTCTGCCTAGAATTCTTTATCTCTTC CAAACTTTTTCCTGCCTCATGACTTTTTAAACTGGTTCCTTCTGCCTAGAATTCTTTATCTCTTC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:102603525..102603642 26863196 MeRIP-seq:(Medium) rs1033537242 Functional Loss SNV dbSNP153 33..33 33 - - - 109318 RMVar_ID_109318 Human_SNP_ID_543368732 m1A Human chr13 + 102604851 102604851 102604851 CGTTGATATCATTGATACAACAGGAAGTGGCGATGTGAATACTGCTACAGAAGTAGAGCCAAAGG CGTTGATATCATTGATACAACAGGAAGTGGCGTTGTGAATACTGCTACAGAAGTAGAGCCAAAGG A T TPP2 Ensembl:ENSG00000134900 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:102604750..102604855 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1804203,Human_RBP_ID_3944155 Human_Splice_Rec_1479524,Human_Splice_Rec_1479525,Human_Splice_Rec_1479582,Human_Splice_Rec_1479583,Human_Splice_Rec_1479636,Human_Splice_Rec_1479637,Human_Splice_Rec_1479692,Human_Splice_Rec_1479693,Human_Splice_Rec_1479744,Human_Splice_Rec_1479745,Human_Splice_Rec_1479748,Human_Splice_Rec_1479749,Human_Splice_Rec_1479799 RMVar_hsa_circ_17415,RMVar_hsa_circ_42452,RMVar_hsa_circ_59980,RMVar_hsa_circ_29408 109319 RMVar_ID_109319 Human_SNP_ID_543413492 m1A Human chr13 - 102773729 102773729 102773729 CGGTCGCTTCGAGCGCGCTAGTCAGCTCCCTGAAGGGAGTGACGGCGGTTGGGTGCCCGCGGCCA CGGTCGCTTCGAGCGCGCTAGTCAGCTCCCTGCAGGGAGTGACGGCGGTTGGGTGCCCGCGGCCA T G TEX30 Ensembl:ENSG00000151287 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr13:102773680..102773760;chr13:102773333..102773731 26863196 MeRIP-seq:(Medium) rs946400324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1480540,Human_RBP_ID_4276678,Human_RBP_ID_18417878 Human_Splice_Rec_1479925,Human_Splice_Rec_1479949,Human_Splice_Rec_1479955,Human_Splice_Rec_1479963 109320 RMVar_ID_109320 Human_SNP_ID_543431339 m1A Human chr13 - 102846498 102846498 102846498 CGGGGATACCGAGGGACGACTGTACTTAGAAAACCTAGTGACAGAGATTCTATAGCGACCCCGAC CGGGGATACCGAGGGACGACTGTACTTAGAAACCCTAGTGACAGAGATTCTATAGCGACCCCGAC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:102846451..102846593 26863196 MeRIP-seq:(Medium) rs1251286714 Functional Loss SNV dbSNP153 33..33 33 - - - 109321 RMVar_ID_109321 Human_SNP_ID_543432329 m1A Human chr13 - 102850348 102850348 102850348 AGGTTCTTCTCACATGCTGCTTCCTCTGCCTGAAACAGTTTCTCCCTCTCTCCGCCTAGTTCTCT AGGTTCTTCTCACATGCTGCTTCCTCTGCCTGGAACAGTTTCTCCCTCTCTCCGCCTAGTTCTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:102850302..102850461 26863196 MeRIP-seq:(Medium) rs1464476417 Functional Loss SNV dbSNP153 33..33 33 - - - 109322 RMVar_ID_109322 Human_SNP_ID_543432427 m1A Human chr13 + 102850842 102850842 102850842 CATGGAGTCAGGGCGTGGTGTATGTGGAGGGGAGTGGAGGTTGATAGTTCAGACAGGAGGAAAGA CATGGAGTCAGGGCGTGGTGTATGTGGAGGGGGGTGGAGGTTGATAGTTCAGACAGGAGGAAAGA A G ERCC5,BIVM-ERCC5 Ensembl:ENSG00000134899,Ensembl:ENSG00000270181 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:102850794..102850902 26863196 MeRIP-seq:(Medium) rs998235198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6255172,Human_RBP_ID_23584135 RMVar_hsa_circ_164592,RMVar_hsa_circ_97419,RMVar_hsa_circ_56392,RMVar_hsa_circ_86825,RMVar_hsa_circ_164606 109323 RMVar_ID_109323 Human_SNP_ID_543435373 m1A Human chr13 + 102862416 102862416 102862416 GAGGGCCAGGAGCAGAAGAAATGCGTATAAACAGCTCCACCGAGAACAGTGATGAAGGACTTAAA GAGGGCCAGGAGCAGAAGAAATGCGTATAAACGGCTCCACCGAGAACAGTGATGAAGGACTTAAA A G ERCC5,BIVM-ERCC5 Ensembl:ENSG00000134899,Ensembl:ENSG00000270181 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:102862368..102862480 26863196 MeRIP-seq:(Medium) rs1385544329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62106,RMVar_hsa_circ_164592,RMVar_hsa_circ_97419,RMVar_hsa_circ_86825,RMVar_hsa_circ_164606,RMVar_hsa_circ_164611,RMVar_hsa_circ_282124,RMVar_hsa_circ_377124,RMVar_hsa_circ_266369,RMVar_hsa_circ_63031,RMVar_hsa_circ_366559,RMVar_hsa_circ_22198 109324 RMVar_ID_109324 Human_SNP_ID_543435490 m1A Human chr13 - 102862696 102862696 102862696 GAGATGCCGGTGTCAGTTCCCTTCCATTCGGGAGCCCAGGTGCGTCACTATGTCTAACCACTGCA GAGATGCCGGTGTCAGTTCCCTTCCATTCGGGGGCCCAGGTGCGTCACTATGTCTAACCACTGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:102862647..102862747 32194978 MeRIP-seq:(Medium) rs1266278644 Functional Loss SNV dbSNP153 33..33 33 - - - 109325 RMVar_ID_109325 Human_SNP_ID_543588991 m1A Human chr13 + 103464911 103464911 103464911 AGAGTTGGGGGCATAAGAAATGCTGGTGGTCTACTCCTGGGGAGACACTGAAGCATTTGGTTGGC AGAGTTGGGGGCATAAGAAATGCTGGTGGTCTGCTCCTGGGGAGACACTGAAGCATTTGGTTGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:103464761..103464985 26863196 MeRIP-seq:(Medium) rs887913507 Functional Loss SNV dbSNP153 33..33 33 - - - 109326 RMVar_ID_109326 Human_SNP_ID_543600223 m1A Human chr13 + 103509287 103509287 103509287 TAAAATAGAATAAGAGGTGAGGCGAGGTGGGCAAGTGAGAGAAGTTTGCAGGAGTGGAGAGGAGA TAAAATAGAATAAGAGGTGAGGCGAGGTGGGCGAGTGAGAGAAGTTTGCAGGAGTGGAGAGGAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:103509206..103509428 26863196 MeRIP-seq:(Medium) rs1566382895 Functional Loss SNV dbSNP153 33..33 33 - - - 109327 RMVar_ID_109327 Human_SNP_ID_372638475 m1A Human chr8 - 90001517 90001517 90001517 GAGGCCACAGGGCAGCCGGGACCCCAGAGTAAAGAAAACCCTGGCCGGTAGCTTCATGTTGAGTC GAGGCCACAGGGCAGCCGGGACCCCAGAGTAATGAAAACCCTGGCCGGTAGCTTCATGTTGAGTC T A NBN Ensembl:ENSG00000104320 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:90001467..90005333 26863196 MeRIP-seq:(Medium) rs766851097 Functional Loss SNV dbSNP153 33..33 33 - - - 109328 RMVar_ID_109328 Human_SNP_ID_372638556 m1A Human chr8 + 90001714 90001714 90001714 GACAGGGCGTCCCGGGGGTTCGGGGAGCGAGGACAGGGCATCCCGAGGCGCAGAGAGAGAGAGGA GACAGGGCGTCCCGGGGGTTCGGGGAGCGAGGGCAGGGCATCCCGAGGCGCAGAGAGAGAGAGGA A G DECR1 Ensembl:ENSG00000104325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:90001422..90002012 26863196 MeRIP-seq:(Medium) rs535744741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796661,Human_RBP_ID_5223788,Human_RBP_ID_5406604,Human_RBP_ID_26795469 109329 RMVar_ID_109329 Human_SNP_ID_372793325 m1A Human chr8 - 90645542 90645542 90645542 GCTGCTGCCTCGGCAGCACCTGTTGGTGCCGGAGCCTCGTGCTGGTCTGCGTGTTGGCCGCCCTG GCTGCTGCCTCGGCAGCACCTGTTGGTGCCGGGGCCTCGTGCTGGTCTGCGTGTTGGCCGCCCTG T C TMEM64 Ensembl:ENSG00000180694 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:90645495..90645601 32194978 MeRIP-seq:(Medium) rs984126434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707006,Human_RBP_ID_4995097,Human_RBP_ID_22115058 109330 RMVar_ID_109330 Human_SNP_ID_372793344 m1A Human chr8 + 90645569 90645569 90645569 GAGGCTCCGGCACCAACAGGTGCTGCCGAGGCAGCAGCAGCGCCAGTTTCTCACCTCAGCCACGC GAGGCTCCGGCACCAACAGGTGCTGCCGAGGCTGCAGCAGCGCCAGTTTCTCACCTCAGCCACGC A T LINC00534 Ensembl:ENSG00000253394 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:90645518..90646088 26863196 MeRIP-seq:(Medium) rs754263601 Functional Loss SNV dbSNP153 33..33 33 - - - 109331 RMVar_ID_109331 Human_SNP_ID_372870391 m1A Human chr8 - 90985208 90985208 90985208 CCACCGCGGTCAGCCAGCGGACCAGCGGCAGGAGCCGTTCCCCGACGGGCAGCAGGGCGCTCGGC CCACCGCGGTCAGCCAGCGGACCAGCGGCAGGGGCCGTTCCCCGACGGGCAGCAGGGCGCTCGGC T C C8orf88 Ensembl:ENSG00000253250 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:90980455..90985207 26863410 MeRIP-seq:(Medium) rs1006541436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995603,Human_RBP_ID_5481297,Human_RBP_ID_17433888 Human_Splice_Rec_991609 109332 RMVar_ID_109332 Human_SNP_ID_372878631 m1A Human chr8 + 91021377 91021377 91021377 TTACTGGAATACCACTGGCGTCTGGACTGGCAATGGCTGTATATGGAGGTGGGAGCTCCGCTGAA TTACTGGAATACCACTGGCGTCTGGACTGGCAGTGGCTGTATATGGAGGTGGGAGCTCCGCTGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr8:91021327..91024293 26863196 MeRIP-seq:(Medium) rs1217493710 Functional Loss SNV dbSNP153 33..33 33 - - - 109333 RMVar_ID_109333 Human_SNP_ID_372882938 m1A Human chr8 - 91040708 91040708 91040708 GATGGGGTGGACGAACGCTCGCCTCTGCTGTCAGCATCCCACTCCGGAAATGTCACTCCCACCGC GATGGGGTGGACGAACGCTCGCCTCTGCTGTCTGCATCCCACTCCGGAAATGTCACTCCCACCGC T A PIP4P2 Ensembl:ENSG00000155099 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:91040657..91040817 26863196 MeRIP-seq:(Medium) rs775075382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_991619,Human_Splice_Rec_991631,Human_Splice_Rec_991637,Human_Splice_Rec_991647,Human_Splice_Rec_991659,Human_Splice_Rec_991673 Human_miRNA_ID_2948986 RMVar_hsa_circ_253010,RMVar_hsa_circ_111235 109334 RMVar_ID_109334 Human_SNP_ID_372882939 m1A Human chr8 - 91040708 91040708 91040708 GATGGGGTGGACGAACGCTCGCCTCTGCTGTCAGCATCCCACTCCGGAAATGTCACTCCCACCGC GATGGGGTGGACGAACGCTCGCCTCTGCTGTCGGCATCCCACTCCGGAAATGTCACTCCCACCGC T C PIP4P2 Ensembl:ENSG00000155099 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:91040657..91040817 26863196 MeRIP-seq:(Medium) rs775075382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_991619,Human_Splice_Rec_991631,Human_Splice_Rec_991637,Human_Splice_Rec_991647,Human_Splice_Rec_991659,Human_Splice_Rec_991673 Human_miRNA_ID_2948986 RMVar_hsa_circ_253010,RMVar_hsa_circ_111235 109335 RMVar_ID_109335 Human_SNP_ID_372882949 m1A Human chr8 + 91040733 91040733 91040733 GGGATGCTGACAGCAGAGGCGAGCGTTCGTCCACCCCATCAGCAGCCATGACTGCGGCAGCGGCG GGGATGCTGACAGCAGAGGCGAGCGTTCGTCCCCCCCATCAGCAGCCATGACTGCGGCAGCGGCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:91040684..91040866 26863196 MeRIP-seq:(Medium) rs756916047 Functional Loss SNV dbSNP153 33..33 33 - - - 109336 RMVar_ID_109336 Human_SNP_ID_372889723 m1A Human chr8 - 91070373 91070373 91070373 TTCGGTCAATACCGCCTCCATGACGACCAGGTACCCCAGCACACGCGCTAGAAGAAACCTGCACC TTCGGTCAATACCGCCTCCATGACGACCAGGTGCCCCAGCACACGCGCTAGAAGAAACCTGCACC T C OTUD6B-AS1 Ensembl:ENSG00000253738 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:91070322..91076635 26863196 MeRIP-seq:(Medium) rs375158776 Functional Loss SNV dbSNP153 33..33 33 - - - 109337 RMVar_ID_109337 Human_SNP_ID_372889724 m1A Human chr8 - 91070373 91070373 91070373 TTCGGTCAATACCGCCTCCATGACGACCAGGTACCCCAGCACACGCGCTAGAAGAAACCTGCACC TTCGGTCAATACCGCCTCCATGACGACCAGGTCCCCCAGCACACGCGCTAGAAGAAACCTGCACC T G OTUD6B-AS1 Ensembl:ENSG00000253738 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:91070322..91076635 26863196 MeRIP-seq:(Medium) rs375158776 Functional Loss SNV dbSNP153 33..33 33 - - - 109338 RMVar_ID_109338 Human_SNP_ID_372889991 m1A Human chr8 + 91071188 91071188 91071188 AGAATGCTGTTCCCAAGAATGACAAGAAGAGGAGGAAGCAACTCACCGAAGATGTGGCCAAGTTG AGAATGCTGTTCCCAAGAATGACAAGAAGAGGCGGAAGCAACTCACCGAAGATGTGGCCAAGTTG A C OTUD6B Ensembl:ENSG00000155100 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:91071104..91071213 26863196 MeRIP-seq:(Medium) rs755136340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957794,Human_RBP_ID_9405582,Human_RBP_ID_19022955,Human_RBP_ID_21995530,Human_RBP_ID_23088100,Human_RBP_ID_24549390,Human_RBP_ID_26359208,Human_RBP_ID_27831402 Human_Splice_Rec_991696,Human_Splice_Rec_991708,Human_Splice_Rec_991722,Human_Splice_Rec_991734,Human_Splice_Rec_991748,Human_Splice_Rec_991760 RMVar_hsa_circ_38357 109339 RMVar_ID_109339 Human_SNP_ID_373440691 m1A Human chr8 + 93341831 93341831 93341831 AGTGTTAAGAGATTTCCTAAAGTAAACAAGCCAGGCATGATTCCAACTTGTTTTGTTTTTCCAGT AGTGTTAAGAGATTTCCTAAAGTAAACAAGCCCGGCATGATTCCAACTTGTTTTGTTTTTCCAGT A C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:93341806..93341888 26863410 MeRIP-seq:(Medium) rs929034878 Functional Loss SNV dbSNP153 33..33 33 - - - 109340 RMVar_ID_109340 Human_SNP_ID_373531596 m1A Human chr8 - 93734486 93734486 93734486 GGAGGAGGATTTCAGGCGGTCTCCCACGGAGGACTTCAGGCAGCTCCCCGAGGAGGACTTCAGGC GGAGGAGGATTTCAGGCGGTCTCCCACGGAGGTCTTCAGGCAGCTCCCCGAGGAGGACTTCAGGC T A RBM12B Ensembl:ENSG00000183808 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:93734426..93734625 26863196 MeRIP-seq:(Medium) rs1299199947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2058039,Human_RBP_ID_7865453,Human_RBP_ID_8922373,Human_RBP_ID_9405587,Human_RBP_ID_22115064,Human_RBP_ID_22731561,Human_RBP_ID_23088104,Human_RBP_ID_23120719,Human_RBP_ID_27127621,Human_RBP_ID_27574585,Human_RBP_ID_27831410 109341 RMVar_ID_109341 Human_SNP_ID_373531616 m1A Human chr8 - 93734550 93734526 93734550 ACTTCAGGCACCCTAGGGAGGAGGACTGGAGGAGGCCCCTTGAGGAGGACTGGAGGCGGCCACTG ACTTCAGGCACCCTAGGGAGGAGGACTGGAGG________________________CGGCCACTG GCCTCCAGTCCTCCTCAAGGGGCCT G RBM12B Ensembl:ENSG00000183808 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:93734426..93734618 26863196 MeRIP-seq:(Medium) rs750983489 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_255554,Human_RBP_ID_796875,Human_RBP_ID_7865456,Human_RBP_ID_9405588,Human_RBP_ID_16490021,Human_RBP_ID_22367540,Human_RBP_ID_22731562,Human_RBP_ID_23088051,Human_RBP_ID_23120719,Human_RBP_ID_27127622,Human_RBP_ID_27574696,Human_RBP_ID_27831410 109342 RMVar_ID_109342 Human_SNP_ID_373659545 m1A Human chr8 - 94262250 94262250 94262250 CCCCGCTCGTTGGCCCGGGTATCCCAGCGCGGACCCACGCGATACGCTGACGCCCCGACGCCGAT CCCCGCTCGTTGGCCCGGGTATCCCAGCGCGGGCCCACGCGATACGCTGACGCCCCGACGCCGAT T C GEM Ensembl:ENSG00000164949 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:94262203..94262289 26863196 MeRIP-seq:(Medium) rs1238053396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_993741,Human_Splice_Rec_993749 109343 RMVar_ID_109343 Human_SNP_ID_373706654 m1A Human chr8 + 94475016 94475016 94475016 CCCCCTGCAGGACGCACCGGCGAAAATCTGACAGAAACCACTGGCCCTGCAAAGAAGTCCTTCTG CCCCCTGCAGGACGCACCGGCGAAAATCTGACGGAAACCACTGGCCCTGCAAAGAAGTCCTTCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94474884..94475015 26863196 MeRIP-seq:(Medium) rs1161548885 Functional Loss SNV dbSNP153 33..33 33 - - - 109344 RMVar_ID_109344 Human_SNP_ID_373719516 m1A Human chr8 - 94527360 94527360 94527360 ACTTAAATATTATTCATACTAATTTTCAGGGGATGATGGTTATGAACAAATTTCCAGTGATGAAG ACTTAAATATTATTCATACTAATTTTCAGGGGCTGATGGTTATGAACAAATTTCCAGTGATGAAG T G VIRMA Ensembl:ENSG00000164944 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94527311..94527401 26863196 MeRIP-seq:(Medium) rs565836368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_217794,Human_RBP_ID_845694,Human_RBP_ID_958194,Human_RBP_ID_1700103,Human_RBP_ID_3973974,Human_RBP_ID_5534227,Human_RBP_ID_8238701,Human_RBP_ID_9405591,Human_RBP_ID_18414371,Human_RBP_ID_19022072,Human_RBP_ID_19029755,Human_RBP_ID_21654232,Human_RBP_ID_21995534,Human_RBP_ID_22115862,Human_RBP_ID_23087887,Human_RBP_ID_23117118,Human_RBP_ID_24549393,Human_RBP_ID_26359228,Human_RBP_ID_27831413 Human_Splice_Rec_993864,Human_Splice_Rec_993970 RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_253108,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_253110,RMVar_hsa_circ_80239,RMVar_hsa_circ_253114,RMVar_hsa_circ_357472,RMVar_hsa_circ_105883,RMVar_hsa_circ_253118,RMVar_hsa_circ_299311,RMVar_hsa_circ_350816,RMVar_hsa_circ_124088,RMVar_hsa_circ_80257,RMVar_hsa_circ_253120,RMVar_hsa_circ_253122,RMVar_hsa_circ_79487,RMVar_hsa_circ_253121,RMVar_hsa_circ_37603,RMVar_hsa_circ_125286,RMVar_hsa_circ_53665,RMVar_hsa_circ_84120,RMVar_hsa_circ_253123,RMVar_hsa_circ_253124,RMVar_hsa_circ_253126,RMVar_hsa_circ_374188,RMVar_hsa_circ_287292,RMVar_hsa_circ_253125,RMVar_hsa_circ_253128,RMVar_hsa_circ_108672,RMVar_hsa_circ_347006,RMVar_hsa_circ_253127,RMVar_hsa_circ_372703,RMVar_hsa_circ_319045,RMVar_hsa_circ_253129,RMVar_hsa_circ_253130 109345 RMVar_ID_109345 Human_SNP_ID_373720002 m1A Human chr8 - 94529156 94529156 94529156 TGTGGATGTAGAGGAAGAAGAGGATGAGGATGAGGATGATCGACGAACAGTAGACAGTATTCCTG TGTGGATGTAGAGGAAGAAGAGGATGAGGATGGGGATGATCGACGAACAGTAGACAGTATTCCTG T C VIRMA Ensembl:ENSG00000164944 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:94529051..94529250;chr8:94529041..94529262;chr8:94529028..94529254 26863196 MeRIP-seq:(Medium) rs143837708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88903,Human_RBP_ID_217797,Human_RBP_ID_959240,Human_RBP_ID_1700104,Human_RBP_ID_3174962,Human_RBP_ID_7867161,Human_RBP_ID_9351423,Human_RBP_ID_9405593,Human_RBP_ID_21995536,Human_RBP_ID_23087889,Human_RBP_ID_23117119,Human_RBP_ID_24272383,Human_RBP_ID_24549395,Human_RBP_ID_26359232,Human_RBP_ID_27831415 Human_Splice_Rec_993863,Human_Splice_Rec_993969 RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_253108,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_253110,RMVar_hsa_circ_80239,RMVar_hsa_circ_253114,RMVar_hsa_circ_357472,RMVar_hsa_circ_105883,RMVar_hsa_circ_253118,RMVar_hsa_circ_299311,RMVar_hsa_circ_350816,RMVar_hsa_circ_80257,RMVar_hsa_circ_253122,RMVar_hsa_circ_79487,RMVar_hsa_circ_253121,RMVar_hsa_circ_125286,RMVar_hsa_circ_53665,RMVar_hsa_circ_84120,RMVar_hsa_circ_253123,RMVar_hsa_circ_253124,RMVar_hsa_circ_253126,RMVar_hsa_circ_374188,RMVar_hsa_circ_287292,RMVar_hsa_circ_253125,RMVar_hsa_circ_253128,RMVar_hsa_circ_108672,RMVar_hsa_circ_347006,RMVar_hsa_circ_253127,RMVar_hsa_circ_372703,RMVar_hsa_circ_319045,RMVar_hsa_circ_253129,RMVar_hsa_circ_253130,RMVar_hsa_circ_253132,RMVar_hsa_circ_78387,RMVar_hsa_circ_372937,RMVar_hsa_circ_253131 109346 RMVar_ID_109346 Human_SNP_ID_373724364 m1A Human chr8 - 94546679 94546679 94546679 GGGGGTGAGGGATAAAAGACTACATATTGGGTACAGTGCACACTGCTTGGGAGACAGGTACACTA GGGGGTGAGGGATAAAAGACTACATATTGGGTCCAGTGCACACTGCTTGGGAGACAGGTACACTA T G VIRMA Ensembl:ENSG00000164944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94546678..94546815 26863196 MeRIP-seq:(Medium) rs1449606298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22626638 RMVar_hsa_circ_118727,RMVar_hsa_circ_253137 109347 RMVar_ID_109347 Human_SNP_ID_373726094 m1A Human chr8 + 94553417 94553417 94553417 CTCAGCGCTCGGGTGTTTAAAAGTATCTAAAAATAACAGCTCCATCGCCGAGTCCACCGCCATGT CTCAGCGCTCGGGTGTTTAAAAGTATCTAAAAGTAACAGCTCCATCGCCGAGTCCACCGCCATGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94553324..94553417 26863196 MeRIP-seq:(Medium) rs747761742 Functional Loss SNV dbSNP153 33..33 33 - - - 109348 RMVar_ID_109348 Human_SNP_ID_373769231 m1A Human chr8 + 94719934 94719934 94719934 GAGCGGGCCCCCGGAGGCCGAGGGGTTCGGCGACGCGGAGGGAGGGAGAGTCTGGGCCGCGCGGG GAGCGGGCCCCCGGAGGCCGAGGGGTTCGGCGCCGCGGAGGGAGGGAGAGTCTGGGCCGCGCGGG A C DPY19L4 Ensembl:ENSG00000156162 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:94719802..94726368;chr8:94719885..94726418 26863196 MeRIP-seq:(Medium) rs925653346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795740,Human_RBP_ID_4995103,Human_RBP_ID_9440702,Human_RBP_ID_18426719 Human_Splice_Rec_994211,Human_Splice_Rec_994217,Human_Splice_Rec_994225 RMVar_hsa_circ_110275,RMVar_hsa_circ_253146 109349 RMVar_ID_109349 Human_SNP_ID_373769243 m1A Human chr8 - 94719952 94719952 94719952 CTAGGGCGCCCTGCGGCTCCCGCGCGGCCCAGACTCTCCCTCCCTCCGCGTCGCCGAACCCCTCG CTAGGGCGCCCTGCGGCTCCCGCGCGGCCCAGTCTCTCCCTCCCTCCGCGTCGCCGAACCCCTCG T A RF00017-1304,RF00017-4495,lnc-CCNE2-2 RNACentral:URS0000990DE9,RNACentral:URS0000923EDC,RNACentral:URS0000D59115 SRP RNA,SRP RNA,lincRNA intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:94719902..94726368 26863196 MeRIP-seq:(Medium) rs1207490411 Functional Loss SNV dbSNP153 33..33 33 - - - 109350 RMVar_ID_109350 Human_SNP_ID_373769244 m1A Human chr8 - 94719952 94719952 94719952 CTAGGGCGCCCTGCGGCTCCCGCGCGGCCCAGACTCTCCCTCCCTCCGCGTCGCCGAACCCCTCG CTAGGGCGCCCTGCGGCTCCCGCGCGGCCCAGGCTCTCCCTCCCTCCGCGTCGCCGAACCCCTCG T C RF00017-1304,RF00017-4495,lnc-CCNE2-2 RNACentral:URS0000990DE9,RNACentral:URS0000923EDC,RNACentral:URS0000D59115 SRP RNA,SRP RNA,lincRNA intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:94719902..94726368 26863196 MeRIP-seq:(Medium) rs1207490411 Functional Loss SNV dbSNP153 33..33 33 - - - 109351 RMVar_ID_109351 Human_SNP_ID_373794315 m1A Human chr8 + 94823378 94823378 94823378 TTCCGCATACCCCAGGCACCGGCCCGCATCCAAGTGTCAGGTTGGAGCCGGGAAGCGGCCCTGGT TTCCGCATACCCCAGGCACCGGCCCGCATCCAGGTGTCAGGTTGGAGCCGGGAAGCGGCCCTGGT A G INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:94823327..94823455 26863196 MeRIP-seq:(Medium) rs1410912373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995613,Human_RBP_ID_5481422,Human_RBP_ID_9338307,Human_RBP_ID_18426720 109352 RMVar_ID_109352 Human_SNP_ID_373808833 m1A Human chr8 + 94877743 94877743 94877743 GCCACTCACACCCAAAGCCATGTCTTACTGTCAGGCACAATTGTTCTGTTAGATCTTATACTGCA GCCACTCACACCCAAAGCCATGTCTTACTGTCGGGCACAATTGTTCTGTTAGATCTTATACTGCA A G INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94877695..94877873 26863196 MeRIP-seq:(Medium) rs557836180 Functional Loss SNV dbSNP153 33..33 33 - - - 109353 RMVar_ID_109353 Human_SNP_ID_373808838 m1A Human chr8 - 94877769 94877769 94877769 GGATAGGTTATGGGCAGAGAGTGGGTTGCAGTATAAGATCTAACAGAACAATTGTGCCTGACAGT GGATAGGTTATGGGCAGAGAGTGGGTTGCAGTGTAAGATCTAACAGAACAATTGTGCCTGACAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:94877718..94877869 26863196 MeRIP-seq:(Medium) rs962190825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16495996 109354 RMVar_ID_109354 Human_SNP_ID_373813160 m1A Human chr8 - 94895063 94895063 94895063 CAGGGAGGAAAATCGGGAGGGCTGAGAACTAGACGACTGGGGGTCATGGGTTCCCGCGTTCCGTC CAGGGAGGAAAATCGGGAGGGCTGAGAACTAGGCGACTGGGGGTCATGGGTTCCCGCGTTCCGTC T C CCNE2 Ensembl:ENSG00000175305 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94895061..94895207 26863196 MeRIP-seq:(Medium) rs1004499173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1337001 109355 RMVar_ID_109355 Human_SNP_ID_373813475 m1A Human chr8 + 94895926 94895926 94895926 GCCCAGGGAAGGCATTTCCAGCCCGCCCACCCAGGTATGTATCAACCCTGCTTTCCGGCTCCCTG GCCCAGGGAAGGCATTTCCAGCCCGCCCACCCGGGTATGTATCAACCCTGCTTTCCGGCTCCCTG A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:94895877..94895999 26863196 MeRIP-seq:(Medium) rs1189454423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_994793,Human_Splice_Rec_994807,Human_Splice_Rec_994835 109356 RMVar_ID_109356 Human_SNP_ID_373830785 m1A Human chr8 - 94965535 94965535 94965535 TTATTCCTATGGCCAACCACAGCCTCTTCACAACTTAATCTCCCACCCTTCTACCAAGGTTGTTT TTATTCCTATGGCCAACCACAGCCTCTTCACAGCTTAATCTCCCACCCTTCTACCAAGGTTGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:94965528..94965763 26863196 MeRIP-seq:(Medium) rs1171313680 Functional Loss SNV dbSNP153 33..33 33 - - - 109357 RMVar_ID_109357 Human_SNP_ID_373844542 m1A Human chr8 - 95025171 95025171 95025171 CAGCAGCTCCAGGCAGTAGTGGTCAGTGCCCCAGGCGCCCGGTCCGCTGGCCGCAGCCACGCTCC CAGCAGCTCCAGGCAGTAGTGGTCAGTGCCCCGGGCGCCCGGTCCGCTGGCCGCAGCCACGCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:95025036..95025241;chr8:95025019..95025182 26863196 MeRIP-seq:(Medium) rs866098943 Functional Loss SNV dbSNP153 33..33 33 - - - 109358 RMVar_ID_109358 Human_SNP_ID_373846489 m1A Human chr8 + 95033744 95033744 95033744 AGATCTGAAGGAGGTGAGGGAGTGAGCTGTACAGATATGTGGGCAAAGAGTATTCTAGGCAGAAG AGATCTGAAGGAGGTGAGGGAGTGAGCTGTACCGATATGTGGGCAAAGAGTATTCTAGGCAGAAG A C NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:95033742..95033913 26863196 MeRIP-seq:(Medium) rs1276373988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253221,RMVar_hsa_circ_109215,RMVar_hsa_circ_295371,RMVar_hsa_circ_334443,RMVar_hsa_circ_344427,RMVar_hsa_circ_362150,RMVar_hsa_circ_300382,RMVar_hsa_circ_288756,RMVar_hsa_circ_294707,RMVar_hsa_circ_279702,RMVar_hsa_circ_253223,RMVar_hsa_circ_253225,RMVar_hsa_circ_253226,RMVar_hsa_circ_253224,RMVar_hsa_circ_253222 109359 RMVar_ID_109359 Human_SNP_ID_373848140 m1A Human chr8 + 95040341 95040341 95040341 CAATTCGTCTACCTGTCCTTTATGGCACTGTTAATTTTTATTACTTAGTCACAATTTTGCCTGGT CAATTCGTCTACCTGTCCTTTATGGCACTGTTTATTTTTATTACTTAGTCACAATTTTGCCTGGT A T NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:95040319..95040406 26863410 MeRIP-seq:(Medium) rs1193175985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253221,RMVar_hsa_circ_109215,RMVar_hsa_circ_295371,RMVar_hsa_circ_362150,RMVar_hsa_circ_300382,RMVar_hsa_circ_288756,RMVar_hsa_circ_294707,RMVar_hsa_circ_279702,RMVar_hsa_circ_253223,RMVar_hsa_circ_253224,RMVar_hsa_circ_253222,RMVar_hsa_circ_253227,RMVar_hsa_circ_317701,RMVar_hsa_circ_356753,RMVar_hsa_circ_327074,RMVar_hsa_circ_364146,RMVar_hsa_circ_355175,RMVar_hsa_circ_12699,RMVar_hsa_circ_125495,RMVar_hsa_circ_253228,RMVar_hsa_circ_253229 109360 RMVar_ID_109360 Human_SNP_ID_373870765 m1A Human chr8 + 95133873 95133873 95133873 TGCGAGCGGCTGCGCTGGCGGCCAGCCCGCCCACCGCGTCTGGATCGCGCCGGCTGCGCGGGGCT TGCGAGCGGCTGCGCTGGCGGCCAGCCCGCCCTCCGCGTCTGGATCGCGCCGGCTGCGCGGGGCT A T PLEKHF2 Ensembl:ENSG00000175895 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:95133808..95133939 26863196 MeRIP-seq:(Medium) rs1408755425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996228,Human_RBP_ID_18426863,Human_RBP_ID_23088053 RMVar_hsa_circ_90044,RMVar_hsa_circ_253233 109361 RMVar_ID_109361 Human_SNP_ID_373870770 m1A Human chr8 + 95133884 95133884 95133884 GCGCTGGCGGCCAGCCCGCCCACCGCGTCTGGATCGCGCCGGCTGCGCGGGGCTGCGGACAGCAC GCGCTGGCGGCCAGCCCGCCCACCGCGTCTGGGTCGCGCCGGCTGCGCGGGGCTGCGGACAGCAC A G PLEKHF2 Ensembl:ENSG00000175895 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:95133839..95134062 26863196 MeRIP-seq:(Medium) rs994236616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995108,Human_RBP_ID_18426863,Human_RBP_ID_23088053 RMVar_hsa_circ_90044,RMVar_hsa_circ_253233 109362 RMVar_ID_109362 Human_SNP_ID_373870792 m1A Human chr8 + 95133948 95133948 95133948 CACACCCTGGAAGGCCCCGGCGGGGAACGGGCAGAGTCCGCGCCCTGCGTCCGCGACCAGGAGGA CACACCCTGGAAGGCCCCGGCGGGGAACGGGCGGAGTCCGCGCCCTGCGTCCGCGACCAGGAGGA A G PLEKHF2 Ensembl:ENSG00000175895 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:95133815..95134010 26863410 MeRIP-seq:(Medium) rs1181003043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845819,Human_RBP_ID_4995619,Human_RBP_ID_8923573,Human_RBP_ID_9313554,Human_RBP_ID_18426863,Human_RBP_ID_23087960 Human_Splice_Rec_995057 RMVar_hsa_circ_90044,RMVar_hsa_circ_253233 109363 RMVar_ID_109363 Human_SNP_ID_373870930 m1A Human chr8 + 95134373 95134373 95134373 GGTCCACGGGTCTGCGGGGCGGGGGCCGGCGGACGCGGGAAGGAGCCCCGAGGCCGGGCGAGAAG GGTCCACGGGTCTGCGGGGCGGGGGCCGGCGGCCGCGGGAAGGAGCCCCGAGGCCGGGCGAGAAG A C PLEKHF2 Ensembl:ENSG00000175895 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:95134281..95134410 26863196 MeRIP-seq:(Medium) rs1327885608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844992,Human_RBP_ID_5328878,Human_RBP_ID_9338310,Human_RBP_ID_17433896,Human_RBP_ID_18466775,Human_RBP_ID_18505645,Human_RBP_ID_19142440,Human_RBP_ID_22115489,Human_RBP_ID_26795093 RMVar_hsa_circ_90044,RMVar_hsa_circ_253233 109364 RMVar_ID_109364 Human_SNP_ID_373901696 m1A Human chr8 + 95268874 95268874 95268874 GAGGTGCCAGAATCCGCGAAGAGGGTCGACGAATGCGCTGCCGCGGAGGGTAGGGCGCTGAGGGT GAGGTGCCAGAATCCGCGAAGAGGGTCGACGACTGCGCTGCCGCGGAGGGTAGGGCGCTGAGGGT A C C8orf37-AS1 Ensembl:ENSG00000253773 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:95268867..95268984 26863196 MeRIP-seq:(Medium) rs1375151514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_995065,Human_Splice_Rec_995071,Human_Splice_Rec_995079 109365 RMVar_ID_109365 Human_SNP_ID_373901819 m1A Human chr8 - 95269097 95269097 95269097 CTTCTAAGACGGGGTATGGTCGAGCAGCCCAAAGGCTGCGGCGGCGGCACCCACAGTAGCGACCG CTTCTAAGACGGGGTATGGTCGAGCAGCCCAACGGCTGCGGCGGCGGCACCCACAGTAGCGACCG T G C8orf37 Ensembl:ENSG00000156172 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:95269048..95269176 26863196 MeRIP-seq:(Medium) rs1004710181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_995117 109366 RMVar_ID_109366 Human_SNP_ID_373902137 m1A Human chr8 - 95269672 95269672 95269672 GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGAATCCTGCCGACTACGGGAATGTCAGCTTTTTG GAAATCCATTGGGGTCTCCCCGCGCAGGTTCGGATCCTGCCGACTACGGGAATGTCAGCTTTTTG T C tRNA-Ser-AGA-2-6 RNACentral:URS000038D8D3 tRNA exon GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1441737303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1699867,Human_RBP_ID_4996827,Human_RBP_ID_5277486,Human_RBP_ID_5430694,Human_RBP_ID_5481318,Human_RBP_ID_5515253,Human_RBP_ID_7868404,Human_RBP_ID_8692414,Human_RBP_ID_9229591,Human_RBP_ID_17434775,Human_RBP_ID_18203240,Human_RBP_ID_21658204,Human_RBP_ID_22837403,Human_RBP_ID_23141079,Human_RBP_ID_24272931,Human_RBP_ID_24521383,Human_RBP_ID_27540165 109367 RMVar_ID_109367 Human_SNP_ID_374133988 m1A Human chr8 - 96231073 96231073 96231073 AAAGAGGTTATTCGGGAAAGAAAAGAAAGAGAAGAATGGGCAAAGAAGTAATCATGTAGTTGAAG AAAGAGGTTATTCGGGAAAGAAAAGAAAGAGACGAATGGGCAAAGAAGTAATCATGTAGTTGAAG T G UQCRB Ensembl:ENSG00000156467 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:96231051..96231125 26863196 MeRIP-seq:(Medium) rs757560966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9405601,Human_RBP_ID_23087961,Human_RBP_ID_26359241,Human_RBP_ID_27831430 Human_Splice_Rec_995148,Human_Splice_Rec_995156,Human_Splice_Rec_995164,Human_Splice_Rec_995166,Human_Splice_Rec_995172,Human_Splice_Rec_995182 109368 RMVar_ID_109368 Human_SNP_ID_374134312 m1A Human chr8 + 96231934 96231934 96231934 CATCTTCATCCTCGTATATTGTATCATCTCGCATTAACCCTATGATAGATGACAAAGTTAGATTG CATCTTCATCCTCGTATATTGTATCATCTCGCGTTAACCCTATGATAGATGACAAAGTTAGATTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:96231789..96231990;chr8:96231784..96231974 26863196 MeRIP-seq:(Medium) rs1261284544 Functional Loss SNV dbSNP153 33..33 33 - - - 109369 RMVar_ID_109369 Human_SNP_ID_374134316 m1A Human chr8 - 96231942 96231942 96231942 TGCATGTGCAATCTAACTTTGTCATCTATCATAGGGTTAATGCGAGATGATACAATATACGAGGA TGCATGTGCAATCTAACTTTGTCATCTATCATTGGGTTAATGCGAGATGATACAATATACGAGGA T A UQCRB Ensembl:ENSG00000156467 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:96231901..96231950 32194978 MeRIP-seq:(Medium) rs111646807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9406393,Human_RBP_ID_18125016 109370 RMVar_ID_109370 Human_SNP_ID_374134317 m1A Human chr8 - 96231942 96231942 96231942 TGCATGTGCAATCTAACTTTGTCATCTATCATAGGGTTAATGCGAGATGATACAATATACGAGGA TGCATGTGCAATCTAACTTTGTCATCTATCATGGGGTTAATGCGAGATGATACAATATACGAGGA T C UQCRB Ensembl:ENSG00000156467 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:96231901..96231950 32194978 MeRIP-seq:(Medium) rs111646807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9406393,Human_RBP_ID_18125016 109371 RMVar_ID_109371 Human_SNP_ID_374142081 m1A Human chr8 - 96261504 96261504 96261504 GGGGTCACCCGCTACGGGAAGCAGGCCTCGCCACAGGTAAAGCAGGAGCTGCCCCAGCACGAGGA GGGGTCACCCGCTACGGGAAGCAGGCCTCGCCTCAGGTAAAGCAGGAGCTGCCCCAGCACGAGGA T A MTERF3 Ensembl:ENSG00000156469 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:96261501..96261600 26863410 MeRIP-seq:(Medium) rs1375291332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994207,Human_RBP_ID_18426723,Human_RBP_ID_19140255 Human_Splice_Rec_995201,Human_Splice_Rec_995217,Human_Splice_Rec_995249 RMVar_hsa_circ_115725,RMVar_hsa_circ_253241 109372 RMVar_ID_109372 Human_SNP_ID_374142106 m1A Human chr8 + 96261562 96261562 96261562 TGACCCCGGGACCGACCAACTCGCTGGGCCGCACGTCCCGTCCCGCCGCGCCGCACGCCGGCTCC TGACCCCGGGACCGACCAACTCGCTGGGCCGCGCGTCCCGTCCCGCCGCGCCGCACGCCGGCTCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:96261458..96261563 26863196 MeRIP-seq:(Medium) rs999716173 Functional Loss SNV dbSNP153 33..33 33 - - - 109373 RMVar_ID_109373 Human_SNP_ID_374142321 m1A Human chr8 + 96262015 96262015 96262015 GGTCCCGGCCTTCTCGGGCTGGGGCCGCCGCCACCGCGGCAGGACGGGGAGGCGGGCCATGGCGT GGTCCCGGCCTTCTCGGGCTGGGGCCGCCGCCCCCGCGGCAGGACGGGGAGGCGGGCCATGGCGT A C PTDSS1 Ensembl:ENSG00000156471 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:96261964..96273343 32194978 MeRIP-seq:(Medium) rs759325615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994218,Human_RBP_ID_5243505,Human_RBP_ID_26832855 Human_miRNA_ID_1967181 RMVar_hsa_circ_253242,RMVar_hsa_circ_78932,RMVar_hsa_circ_109954,RMVar_hsa_circ_253243 109374 RMVar_ID_109374 Human_SNP_ID_374147932 m1A Human chr8 + 96287134 96287134 96287134 CTAGATCCAAATCTTCGATACGCCACAAGGGAAGCAGATGTCATGGTATGTACTTGTCAGTGGCC CTAGATCCAAATCTTCGATACGCCACAAGGGAGGCAGATGTCATGGTATGTACTTGTCAGTGGCC A G PTDSS1 Ensembl:ENSG00000156471 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:96287084..96287202 26863196 MeRIP-seq:(Medium) rs1244040118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795742,Human_RBP_ID_961077,Human_RBP_ID_17319418,Human_RBP_ID_19140257 Human_Splice_Rec_995259,Human_Splice_Rec_995307 Human_miRNA_ID_2721852 RMVar_hsa_circ_73857,RMVar_hsa_circ_109954,RMVar_hsa_circ_253243,RMVar_hsa_circ_253244,RMVar_hsa_circ_95626,RMVar_hsa_circ_267878,RMVar_hsa_circ_331568,RMVar_hsa_circ_267522,RMVar_hsa_circ_25539,RMVar_hsa_circ_91471,RMVar_hsa_circ_253245 109375 RMVar_ID_109375 Human_SNP_ID_374158898 m1A Human chr8 - 96333698 96333698 96333698 TCTGTGGGAAACAAGACTTACGATCTCAAATAATGACCCCCAAGTGCCCTCGCCTCTTCCTGCTT TCTGTGGGAAACAAGACTTACGATCTCAAATACTGACCCCCAAGTGCCCTCGCCTCTTCCTGCTT T G RF00017-4501 RNACentral:URS0000972B66 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:96333647..96333798 32194978 MeRIP-seq:(Medium) rs748618103 Functional Loss SNV dbSNP153 33..33 33 - - - 109376 RMVar_ID_109376 Human_SNP_ID_374159124 m1A Human chr8 + 96334476 96334476 96334476 AGTATTACCTTTCATCTGTGCCATGCTCTAGAACCTTGACCTTGATAGTTCACCACCTCTGATGG AGTATTACCTTTCATCTGTGCCATGCTCTAGATCCTTGACCTTGATAGTTCACCACCTCTGATGG A T PTDSS1 Ensembl:ENSG00000156471 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:96334197..96334497 32194978 MeRIP-seq:(Medium) rs1309432384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706446,Human_RBP_ID_2058363,Human_RBP_ID_3175410,Human_RBP_ID_16498979,Human_RBP_ID_17547077,Human_RBP_ID_18900769,Human_RBP_ID_21565780,Human_RBP_ID_24273171,Human_RBP_ID_24521298,Human_RBP_ID_26557843,Human_RBP_ID_27570085 Human_miRNA_ID_2797626,Human_miRNA_ID_2798592,Human_miRNA_ID_2799973,Human_miRNA_ID_2807288,Human_miRNA_ID_2810432,Human_miRNA_ID_2813574,Human_miRNA_ID_2833164,Human_miRNA_ID_2852687,Human_miRNA_ID_2853749,Human_miRNA_ID_2860831 RMVar_hsa_circ_109954,RMVar_hsa_circ_253243,RMVar_hsa_circ_253244,RMVar_hsa_circ_95626,RMVar_hsa_circ_267522,RMVar_hsa_circ_101048,RMVar_hsa_circ_91471,RMVar_hsa_circ_253245,RMVar_hsa_circ_118639,RMVar_hsa_circ_125021,RMVar_hsa_circ_253253,RMVar_hsa_circ_253254,RMVar_hsa_circ_253263,RMVar_hsa_circ_92265,RMVar_hsa_circ_91671,RMVar_hsa_circ_253265,RMVar_hsa_circ_117443,RMVar_hsa_circ_253266,RMVar_hsa_circ_253267 109377 RMVar_ID_109377 Human_SNP_ID_374195515 m1A Human chr8 + 96494103 96494103 96494103 CAGCTGCGGGCGGCGGGAGCAGGCGCAGGAGGAGGAAGCGAGCGCCCCCGAGCCCCGAGCCCGAG CAGCTGCGGGCGGCGGGAGCAGGCGCAGGAGGCGGAAGCGAGCGCCCCCGAGCCCCGAGCCCGAG A C SDC2 Ensembl:ENSG00000169439 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:96493649..96529205;chr8:96493651..96494350 26863196 MeRIP-seq:(Medium) rs1026658344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255471,Human_RBP_ID_4995117,Human_RBP_ID_5534231,Human_RBP_ID_9405610,Human_RBP_ID_18472503,Human_RBP_ID_22465241 109378 RMVar_ID_109378 Human_SNP_ID_374461599 m1A Human chr8 + 97644330 97644330 97644330 GGCGGAGTGAGGCTGACAGCGGGGAACCTGGGAGACCCCTCCGCCCTCCCCGCGGTGGCAGCGGC GGCGGAGTGAGGCTGACAGCGGGGAACCTGGGGGACCCCTCCGCCCTCCCCGCGGTGGCAGCGGC A G MTDH Ensembl:ENSG00000147649 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:97644176..97644658;chr8:97644151..97644478;chr8:97644176..97644500 26863196 MeRIP-seq:(Medium) rs1355645406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88608,Human_RBP_ID_4995125,Human_RBP_ID_9405616,Human_RBP_ID_18196733 Human_miRNA_ID_2153211,Human_miRNA_ID_2801085,Human_miRNA_ID_3009213 RMVar_hsa_circ_76057,RMVar_hsa_circ_253286 109379 RMVar_ID_109379 Human_SNP_ID_374461607 m1A Human chr8 + 97644357 97644357 97644357 CTGGGAGACCCCTCCGCCCTCCCCGCGGTGGCAGCGGCCGATCCCCGGCTCCGGCGCGAGGGACG CTGGGAGACCCCTCCGCCCTCCCCGCGGTGGCCGCGGCCGATCCCCGGCTCCGGCGCGAGGGACG A C MTDH Ensembl:ENSG00000147649 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:97644201..97644500 26863196 MeRIP-seq:(Medium) rs1000972723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88608,Human_RBP_ID_254883,Human_RBP_ID_4995125,Human_RBP_ID_9405616,Human_RBP_ID_18196733 RMVar_hsa_circ_76057,RMVar_hsa_circ_253286 109380 RMVar_ID_109380 Human_SNP_ID_374461630 m1A Human chr8 - 97644438 97644438 97644438 GGGGCGCGGAGACGCAGTGGAATAGTCGAGGGAAGCGAGGAAGGGCCGGGCCGGGTAACCTCAGG GGGGCGCGGAGACGCAGTGGAATAGTCGAGGGCAGCGAGGAAGGGCCGGGCCGGGTAACCTCAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr8:97644176..97644831;chr8:97644176..97644500 26863196 MeRIP-seq:(Medium) rs1244921617 Functional Loss SNV dbSNP153 33..33 33 - - - 109381 RMVar_ID_109381 Human_SNP_ID_374461634 m1A Human chr8 - 97644442 97644442 97644442 CGCCGGGGCGCGGAGACGCAGTGGAATAGTCGAGGGAAGCGAGGAAGGGCCGGGCCGGGTAACCT CGCCGGGGCGCGGAGACGCAGTGGAATAGTCGCGGGAAGCGAGGAAGGGCCGGGCCGGGTAACCT T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:97644176..97644525 26863196 MeRIP-seq:(Medium) rs927507669 Functional Loss SNV dbSNP153 33..33 33 - - - 109382 RMVar_ID_109382 Human_SNP_ID_374465845 m1A Human chr8 + 97661170 97661170 97661170 AAGCAGCCACCAGAGATTGACAAGAAAAATGAAAAGGTAAGTTTGGGAGCATATGAAATTGTATG AAGCAGCCACCAGAGATTGACAAGAAAAATGACAAGGTAAGTTTGGGAGCATATGAAATTGTATG A C MTDH Ensembl:ENSG00000147649 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:97661150..97661235 26863196 MeRIP-seq:(Medium) rs763351626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2058398,Human_RBP_ID_9351431 Human_Splice_Rec_995440,Human_Splice_Rec_995441,Human_Splice_Rec_995462,Human_Splice_Rec_995463,Human_Splice_Rec_995482,Human_Splice_Rec_995483 Human_miRNA_ID_1790179 RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_275797,RMVar_hsa_circ_292754,RMVar_hsa_circ_338777,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253291,RMVar_hsa_circ_253292,RMVar_hsa_circ_253289 109383 RMVar_ID_109383 Human_SNP_ID_374473294 m1A Human chr8 + 97687443 97687443 97687443 TTTCTGGGGCTATGTCAGGAGCCTGGGAAACTAAAATTAGTCACAGAGAGAAACGACAGCAGCGT TTTCTGGGGCTATGTCAGGAGCCTGGGAAACTCAAATTAGTCACAGAGAGAAACGACAGCAGCGT A C MTDH Ensembl:ENSG00000147649 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:97687431..97687531 32194978 MeRIP-seq:(Medium) rs775703791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88617,Human_RBP_ID_706537,Human_RBP_ID_3175533,Human_RBP_ID_9405621,Human_RBP_ID_16499893,Human_RBP_ID_27127928 Human_Splice_Rec_995444,Human_Splice_Rec_995466,Human_Splice_Rec_995486 RMVar_hsa_circ_1736,RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_275797,RMVar_hsa_circ_292754,RMVar_hsa_circ_338777,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253291,RMVar_hsa_circ_253292,RMVar_hsa_circ_253289,RMVar_hsa_circ_253295,RMVar_hsa_circ_290744,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_272169,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_253293,RMVar_hsa_circ_253294,RMVar_hsa_circ_96623,RMVar_hsa_circ_253297 109384 RMVar_ID_109384 Human_SNP_ID_374497037 m1A Human chr8 + 97775831 97775831 97775831 TGCAGCGGTCGCCTTCGGAGCGAAGGGTACCGACCCGGCAGAAGCTCGGAGCTCTCGGGGTATCG TGCAGCGGTCGCCTTCGGAGCGAAGGGTACCGCCCCGGCAGAAGCTCGGAGCTCTCGGGGTATCG A C LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:97775776..97776050 26863196 MeRIP-seq:(Medium) rs1273481302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994581,Human_RBP_ID_9338314,Human_RBP_ID_22465252,Human_RBP_ID_22517452 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109385 RMVar_ID_109385 Human_SNP_ID_374497045 m1A Human chr8 - 97775844 97775844 97775844 GGGCCTGCCTCCTCGATACCCCGAGAGCTCCGAGCTTCTGCCGGGTCGGTACCCTTCGCTCCGAA GGGCCTGCCTCCTCGATACCCCGAGAGCTCCGCGCTTCTGCCGGGTCGGTACCCTTCGCTCCGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:97775776..97776100;chr8:97775776..97776075;chr8:97775776..97776050 26863196 MeRIP-seq:(Medium) rs1475107994 Functional Loss SNV dbSNP153 33..33 33 - - - 109386 RMVar_ID_109386 Human_SNP_ID_374497069 m1A Human chr8 + 97775885 97775877 97775885 TCGGGGTATCGAGGAGGCAGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGA TCGGGGTATCGAGGAGGCAGGCCCG________CGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGA GCGGGCGCA G LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:97775786..97775956 26863410 MeRIP-seq:(Medium) rs1194454433 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_254749,Human_RBP_ID_795421,Human_RBP_ID_4994582,Human_RBP_ID_5328879,Human_RBP_ID_8944462,Human_RBP_ID_9338314,Human_RBP_ID_17433898,Human_RBP_ID_18472619,Human_RBP_ID_22464969 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109387 RMVar_ID_109387 Human_SNP_ID_374497074 m1A Human chr8 + 97775885 97775885 97775885 TCGGGGTATCGAGGAGGCAGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGA TCGGGGTATCGAGGAGGCAGGCCCGCGGGCGCGCGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGA A G LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:97775786..97775956 26863410 MeRIP-seq:(Medium) rs1563596436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254749,Human_RBP_ID_795421,Human_RBP_ID_4994582,Human_RBP_ID_5328879,Human_RBP_ID_8944462,Human_RBP_ID_9338314,Human_RBP_ID_17433898,Human_RBP_ID_18472619,Human_RBP_ID_22464969 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109388 RMVar_ID_109388 Human_SNP_ID_374497087 m1A Human chr8 + 97775903 97775903 97775903 AGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGAGGAGCCGGCAGCAGCGGC AGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGCGCCGGAGCGGCGGAGGAGCCGGCAGCAGCGGC A C LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:97775801..97775975 26863410 MeRIP-seq:(Medium) rs771404431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254749,Human_RBP_ID_845814,Human_RBP_ID_4994582,Human_RBP_ID_5328879,Human_RBP_ID_8944462,Human_RBP_ID_9338314,Human_RBP_ID_17433898,Human_RBP_ID_18472619,Human_RBP_ID_22464969 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109389 RMVar_ID_109389 Human_SNP_ID_374497088 m1A Human chr8 + 97775903 97775903 97775903 AGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGAGCCGGAGCGGCGGAGGAGCCGGCAGCAGCGGC AGGCCCGCGGGCGCACGGGCGAGCGGGCCGGGGGCCGGAGCGGCGGAGGAGCCGGCAGCAGCGGC A G LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:97775801..97775975 26863410 MeRIP-seq:(Medium) rs771404431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254749,Human_RBP_ID_845814,Human_RBP_ID_4994582,Human_RBP_ID_5328879,Human_RBP_ID_8944462,Human_RBP_ID_9338314,Human_RBP_ID_17433898,Human_RBP_ID_18472619,Human_RBP_ID_22464969 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109390 RMVar_ID_109390 Human_SNP_ID_374497089 m1A Human chr8 + 97775930 97775905 97775931 CCGGGAGCCGGAGCGGCGGAGGAGCCGGCAGCAGCGGCGCGGCGGGCTCCAGGCGAGGCGGTCGA CCGGGAGC__________________________CGGCGCGGCGGGCTCCAGGCGAGGCGGTCGA CCGGAGCGGCGGAGGAGCCGGCAGCAG C LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:97775832..97775956 26863410 MeRIP-seq:(Medium) rs747938474 Functional Loss DEL dbSNP153 9..34 33 - - - Human_RBP_ID_88098,Human_RBP_ID_254749,Human_RBP_ID_706666,Human_RBP_ID_845814,Human_RBP_ID_4994582,Human_RBP_ID_5328879,Human_RBP_ID_8944462,Human_RBP_ID_9338314,Human_RBP_ID_17433898,Human_RBP_ID_18472619,Human_RBP_ID_22465253 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109391 RMVar_ID_109391 Human_SNP_ID_374497122 m1A Human chr8 - 97775945 97775945 97775945 AAGTTTTCAGGAGCGTCGACCGCCTCGCCTGGAGCCCGCCGCGCCGCTGCTGCCGGCTCCTCCGC AAGTTTTCAGGAGCGTCGACCGCCTCGCCTGGCGCCCGCCGCGCCGCTGCTGCCGGCTCCTCCGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:97775801..97776100 26863410 MeRIP-seq:(Medium) rs1460449296 Functional Loss SNV dbSNP153 33..33 33 - - - 109392 RMVar_ID_109392 Human_SNP_ID_374497126 m1A Human chr8 + 97775948 97775948 97775948 GAGGAGCCGGCAGCAGCGGCGCGGCGGGCTCCAGGCGAGGCGGTCGACGCTCCTGAAAACTTGCG GAGGAGCCGGCAGCAGCGGCGCGGCGGGCTCCTGGCGAGGCGGTCGACGCTCCTGAAAACTTGCG A T LAPTM4B Ensembl:ENSG00000104341 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr8:97775855..97775956 26863410 MeRIP-seq:(Medium) rs1233570925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88098,Human_RBP_ID_254749,Human_RBP_ID_706666,Human_RBP_ID_4994583,Human_RBP_ID_8944462,Human_RBP_ID_22465253 RMVar_hsa_circ_76300,RMVar_hsa_circ_104415,RMVar_hsa_circ_253319,RMVar_hsa_circ_253320 109393 RMVar_ID_109393 Human_SNP_ID_374510806 m1A Human chr8 + 97825854 97825854 97825854 TGTAATGCACAGTACCAGGAAGTGCTCCATGCATGGTTAGTGAAAACGATGGGGATGGATGACAT TGTAATGCACAGTACCAGGAAGTGCTCCATGCGTGGTTAGTGAAAACGATGGGGATGGATGACAT A G LAPTM4B Ensembl:ENSG00000104341 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:97825851..97825960 26863196 MeRIP-seq:(Medium) rs1422159718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8692617 RMVar_hsa_circ_101596,RMVar_hsa_circ_76300,RMVar_hsa_circ_253320,RMVar_hsa_circ_120095,RMVar_hsa_circ_253327,RMVar_hsa_circ_253331,RMVar_hsa_circ_253329,RMVar_hsa_circ_112943,RMVar_hsa_circ_81523,RMVar_hsa_circ_253332 109394 RMVar_ID_109394 Human_SNP_ID_374511613 m1A Human chr8 + 97829109 97829109 97829109 AGAGTGTGTTCTGGAAGTGGGGTCCTGCACCCAGACCCCTAGGGATCCAGCAAGGGTAGCAGCTG AGAGTGTGTTCTGGAAGTGGGGTCCTGCACCCGGACCCCTAGGGATCCAGCAAGGGTAGCAGCTG A G LAPTM4B Ensembl:ENSG00000104341 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:97829103..97829641 26863196 MeRIP-seq:(Medium) rs1268895061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101596,RMVar_hsa_circ_76300,RMVar_hsa_circ_253320,RMVar_hsa_circ_120095,RMVar_hsa_circ_253327,RMVar_hsa_circ_253331,RMVar_hsa_circ_253329,RMVar_hsa_circ_112943,RMVar_hsa_circ_81523,RMVar_hsa_circ_253332 109395 RMVar_ID_109395 Human_SNP_ID_374517503 m1A Human chr8 - 97851404 97851404 97851404 CACCATTCACAGTGGCATCATCATACGGGGGTAGCAGCACCTGAGAAGAAAGAGGGACGGCAAGA CACCATTCACAGTGGCATCATCATACGGGGGTGGCAGCACCTGAGAAGAAAGAGGGACGGCAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:97851398..97851490 26863196 MeRIP-seq:(Medium) rs771294060 Functional Loss SNV dbSNP153 33..33 33 - - - 109396 RMVar_ID_109396 Human_SNP_ID_374517714 m1A Human chr8 - 97852116 97852116 97852116 TACGAGGCATGTCACCCCATGTCCCTGGACACAAGATCCACAAGAACAGTCAGCAGATGGTCACT TACGAGGCATGTCACCCCATGTCCCTGGACACGAGATCCACAAGAACAGTCAGCAGATGGTCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:97852067..97852237 26863196 MeRIP-seq:(Medium) rs1399556989 Functional Loss SNV dbSNP153 33..33 33 - - - 109397 RMVar_ID_109397 Human_SNP_ID_374521851 m1A Human chr8 + 97869137 97869137 97869137 GATGGGACTTGGAGCAAGCGGCGGCGGCGGAGACAGAGGCAGAGGCAGAAGCTGGGGCTCCGTCC GATGGGACTTGGAGCAAGCGGCGGCGGCGGAGGCAGAGGCAGAGGCAGAAGCTGGGGCTCCGTCC A G MATN2 Ensembl:ENSG00000132561 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:97869072..97869243 26863196 MeRIP-seq:(Medium) rs1019165868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994660 109398 RMVar_ID_109398 Human_SNP_ID_374521855 m1A Human chr8 + 97869139 97869139 97869139 TGGGACTTGGAGCAAGCGGCGGCGGCGGAGACAGAGGCAGAGGCAGAAGCTGGGGCTCCGTCCTC TGGGACTTGGAGCAAGCGGCGGCGGCGGAGACGGAGGCAGAGGCAGAAGCTGGGGCTCCGTCCTC A G MATN2 Ensembl:ENSG00000132561 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:97869088..97869239 26863196 MeRIP-seq:(Medium) rs1381286630 Functional Loss SNV dbSNP153 33..33 33 - - - 109399 RMVar_ID_109399 Human_SNP_ID_374536159 m1A Human chr8 + 97931477 97931477 97931477 ATGAGGACCATGTCTTCCTTGTGGCCAATTTCAGCCAGATTGAGACGCTGACCTCCGTGTTCCAG ATGAGGACCATGTCTTCCTTGTGGCCAATTTCGGCCAGATTGAGACGCTGACCTCCGTGTTCCAG A G MATN2 Ensembl:ENSG00000132561 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:97931426..97941843 32194978 MeRIP-seq:(Medium) rs926495800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_995559,Human_Splice_Rec_995593,Human_Splice_Rec_995627,Human_Splice_Rec_995659,Human_Splice_Rec_995703,Human_Splice_Rec_995733,Human_Splice_Rec_995761 Human_miRNA_ID_2331442,Human_miRNA_ID_2964525 RMVar_hsa_circ_13626,RMVar_hsa_circ_361146,RMVar_hsa_circ_361300,RMVar_hsa_circ_357171,RMVar_hsa_circ_253334 109400 RMVar_ID_109400 Human_SNP_ID_374562216 m1A Human chr8 - 98045302 98045302 98045302 GGCCAGGCCCGGAAGACGATTCACGTGGAGAGATGTCTTGGCCAGGGCGGGCAGATGTGAGCCCA GGCCAGGCCCGGAAGACGATTCACGTGGAGAGGTGTCTTGGCCAGGGCGGGCAGATGTGAGCCCA T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:98045291..98045487 26863410 MeRIP-seq:(Medium) rs774051404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706835,Human_RBP_ID_24273663 Human_Splice_Rec_995826,Human_Splice_Rec_995840,Human_Splice_Rec_995848,Human_Splice_Rec_995856,Human_Splice_Rec_995864,Human_Splice_Rec_995870,Human_Splice_Rec_995878,Human_Splice_Rec_995886,Human_Splice_Rec_995890 RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_253337,RMVar_hsa_circ_253338,RMVar_hsa_circ_110366 109401 RMVar_ID_109401 Human_SNP_ID_374562228 m1A Human chr8 - 98045330 98045330 98045330 GGCCGCAAAGAAGACGGTGAGTGAGGCGGGCCAGGCCCGGAAGACGATTCACGTGGAGAGATGTC GGCCGCAAAGAAGACGGTGAGTGAGGCGGGCCGGGCCCGGAAGACGATTCACGTGGAGAGATGTC T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:98045326..98045475 32194978 MeRIP-seq:(Medium) rs551163149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706835,Human_RBP_ID_19141510,Human_RBP_ID_24273664 Human_Splice_Rec_995826,Human_Splice_Rec_995840,Human_Splice_Rec_995848,Human_Splice_Rec_995856,Human_Splice_Rec_995864,Human_Splice_Rec_995870,Human_Splice_Rec_995878,Human_Splice_Rec_995886,Human_Splice_Rec_995890 RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_253337,RMVar_hsa_circ_253338,RMVar_hsa_circ_110366 109402 RMVar_ID_109402 Human_SNP_ID_374562229 m1A Human chr8 - 98045330 98045330 98045330 GGCCGCAAAGAAGACGGTGAGTGAGGCGGGCCAGGCCCGGAAGACGATTCACGTGGAGAGATGTC GGCCGCAAAGAAGACGGTGAGTGAGGCGGGCCCGGCCCGGAAGACGATTCACGTGGAGAGATGTC T G RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:98045326..98045475 32194978 MeRIP-seq:(Medium) rs551163149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706835,Human_RBP_ID_19141510,Human_RBP_ID_24273664 Human_Splice_Rec_995826,Human_Splice_Rec_995840,Human_Splice_Rec_995848,Human_Splice_Rec_995856,Human_Splice_Rec_995864,Human_Splice_Rec_995870,Human_Splice_Rec_995878,Human_Splice_Rec_995886,Human_Splice_Rec_995890 RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_253337,RMVar_hsa_circ_253338,RMVar_hsa_circ_110366 109403 RMVar_ID_109403 Human_SNP_ID_374562245 m1A Human chr8 + 98045379 98045379 98045379 CGTCTTCTTTGCGGCCACCATCTTCCTGCCTTAGGAGCGGGACGGCCCCCAACCTAGAAGAGACA CGTCTTCTTTGCGGCCACCATCTTCCTGCCTTGGGAGCGGGACGGCCCCCAACCTAGAAGAGACA A G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:98045201..98045380 26863196 MeRIP-seq:(Medium) rs10591 Functional Loss SNV dbSNP153 33..33 33 - - - 109404 RMVar_ID_109404 Human_SNP_ID_374562247 m1A Human chr8 + 98045388 98045387 98045389 TGCGGCCACCATCTTCCTGCCTTAGGAGCGGGACGGCCCCCAACCTAGAAGAGACAGAGAACAGG TGCGGCCACCATCTTCCTGCCTTAGGAGCGGG__GGCCCCCAACCTAGAAGAGACAGAGAACAGG GAC G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98045176..98045575 26863196 MeRIP-seq:(Medium) rs1204492154 Functional Loss DEL dbSNP153 33..34 33 - - - 109405 RMVar_ID_109405 Human_SNP_ID_374577151 m1A Human chr8 - 98102845 98102845 98102845 GCTATCCAAGGACCACTGACAACGGCATCACTATAAGTGGGCCCAGTGCTGTGTAGTCTGGAATT GCTATCCAAGGACCACTGACAACGGCATCACTGTAAGTGGGCCCAGTGCTGTGTAGTCTGGAATT T C RIDA Ensembl:ENSG00000132541 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs370041963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706862,Human_RBP_ID_9229780 Human_Splice_Rec_995908,Human_Splice_Rec_995918,Human_Splice_Rec_995928,Human_Splice_Rec_995936,Human_Splice_Rec_995942 109406 RMVar_ID_109406 Human_SNP_ID_374580439 m1A Human chr8 - 98117111 98117111 98117111 GCTGGGGCTTCTTCTCCTGAAGGGGCTGCAAGAGGGAAGGCTTAGCCATGTCGTCCTTGATCAGA GCTGGGGCTTCTTCTCCTGAAGGGGCTGCAAGTGGGAAGGCTTAGCCATGTCGTCCTTGATCAGA T A RIDA Ensembl:ENSG00000132541 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98117000..98117121 26863196 MeRIP-seq:(Medium) rs563267746 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_706873,Human_RBP_ID_4995645,Human_RBP_ID_18426727 Human_Splice_Rec_995899,Human_Splice_Rec_995909,Human_Splice_Rec_995919,Human_Splice_Rec_995929,Human_Splice_Rec_995943 109407 RMVar_ID_109407 Human_SNP_ID_374580575 m1A Human chr8 + 98117389 98117389 98117389 TTCTGACCCGGGGATTCCTCACAGCGTCTGGCAGGTTGGTCGTGAGGGGCTGGTGCCTTCCAGGA TTCTGACCCGGGGATTCCTCACAGCGTCTGGCTGGTTGGTCGTGAGGGGCTGGTGCCTTCCAGGA A T POP1 Ensembl:ENSG00000104356 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98117372..98117442 26863196 MeRIP-seq:(Medium) rs910904966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995646,Human_RBP_ID_19141512 Human_Splice_Rec_995945 109408 RMVar_ID_109408 Human_SNP_ID_374712825 m1A Human chr8 - 98679366 98679365 98679366 GAAGATGATACTGGAATAAAAAGCTGAAGAAAATGAGGGTATCTGGATGTAGAATATCTAGGCAG GAAGATGATACTGGAATAAAAAGCTGAAGAAA_TGAGGGTATCTGGATGTAGAATATCTAGGCAG AT A STK3 Ensembl:ENSG00000104375 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:98679362..98679459 26863196 MeRIP-seq:(Medium) rs900799132 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_14533,RMVar_hsa_circ_124809,RMVar_hsa_circ_91991,RMVar_hsa_circ_94068,RMVar_hsa_circ_253359,RMVar_hsa_circ_253360,RMVar_hsa_circ_253358,RMVar_hsa_circ_56082,RMVar_hsa_circ_76036,RMVar_hsa_circ_50829,RMVar_hsa_circ_253369,RMVar_hsa_circ_74314,RMVar_hsa_circ_56336,RMVar_hsa_circ_95924,RMVar_hsa_circ_360841,RMVar_hsa_circ_253371,RMVar_hsa_circ_253372 109409 RMVar_ID_109409 Human_SNP_ID_374712826 m1A Human chr8 - 98679366 98679366 98679366 GAAGATGATACTGGAATAAAAAGCTGAAGAAAATGAGGGTATCTGGATGTAGAATATCTAGGCAG GAAGATGATACTGGAATAAAAAGCTGAAGAAAGTGAGGGTATCTGGATGTAGAATATCTAGGCAG T C STK3 Ensembl:ENSG00000104375 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:98679362..98679459 26863196 MeRIP-seq:(Medium) rs1286699145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14533,RMVar_hsa_circ_124809,RMVar_hsa_circ_91991,RMVar_hsa_circ_94068,RMVar_hsa_circ_253359,RMVar_hsa_circ_253360,RMVar_hsa_circ_253358,RMVar_hsa_circ_56082,RMVar_hsa_circ_76036,RMVar_hsa_circ_50829,RMVar_hsa_circ_253369,RMVar_hsa_circ_74314,RMVar_hsa_circ_56336,RMVar_hsa_circ_95924,RMVar_hsa_circ_360841,RMVar_hsa_circ_253371,RMVar_hsa_circ_253372 109410 RMVar_ID_109410 Human_SNP_ID_374749244 m1A Human chr8 - 98825624 98825624 98825624 CGAGTTCCCAGAGTTTCCCTCTGTGGTGCCCTAGGCTCGGCCGGCCGGTGCCCCGGCTCCTTTCC CGAGTTCCCAGAGTTTCCCTCTGTGGTGCCCTGGGCTCGGCCGGCCGGTGCCCCGGCTCCTTTCC T C STK3 Ensembl:ENSG00000104375 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98825469..98825663 26863196 MeRIP-seq:(Medium) rs1395912775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995647,Human_RBP_ID_18427105 RMVar_hsa_circ_124809,RMVar_hsa_circ_253358,RMVar_hsa_circ_97793,RMVar_hsa_circ_253379 109411 RMVar_ID_109411 Human_SNP_ID_374777840 m1A Human chr8 + 98944525 98944525 98944525 AGGGTGATGGCCCTGCAAGGCTGTGGGCTCCGACCTCACCGGGAGTCGACAGCGAGAGGTTCGCC AGGGTGATGGCCCTGCAAGGCTGTGGGCTCCGCCCTCACCGGGAGTCGACAGCGAGAGGTTCGCC A C OSR2 Ensembl:ENSG00000164920 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98944475..98944708 26863196 MeRIP-seq:(Medium) rs542370359 Functional Loss SNV dbSNP153 33..33 33 - - - 109412 RMVar_ID_109412 Human_SNP_ID_374778933 m1A Human chr8 + 98948934 98948934 98948934 GATTCCTGGAAGAAAGGGTTGGTCCCCTCAGCACCCCCAGCATCCCGGAAAATGGGGAGCAAGGC GATTCCTGGAAGAAAGGGTTGGTCCCCTCAGCCCCCCCAGCATCCCGGAAAATGGGGAGCAAGGC A C OSR2 Ensembl:ENSG00000164920 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98948886..98948995 26863196 MeRIP-seq:(Medium) rs186206047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_996272,Human_Splice_Rec_996278,Human_Splice_Rec_996282,Human_Splice_Rec_996292,Human_Splice_Rec_996300,Human_Splice_Rec_996306,Human_Splice_Rec_996308 109413 RMVar_ID_109413 Human_SNP_ID_375003420 m1A Human chr8 - 99887563 99887563 99887563 GAAGGCATACGCAGATTTCTACAGAAACTACGATGTCATGAAAGATTTTGAGGAGATGAGGAAGG GAAGGCATACGCAGATTTCTACAGAAACTACGGTGTCATGAAAGATTTTGAGGAGATGAGGAAGG T C COX6C Ensembl:ENSG00000164919 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:99887513..99887667 26863196 MeRIP-seq:(Medium) rs1219288040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89902,Human_RBP_ID_691696,Human_RBP_ID_1053775,Human_RBP_ID_2050593,Human_RBP_ID_9218137,Human_RBP_ID_17665990,Human_RBP_ID_22464975,Human_RBP_ID_24237573 Human_Splice_Rec_996738,Human_Splice_Rec_996739,Human_Splice_Rec_996746,Human_Splice_Rec_996747,Human_Splice_Rec_996754,Human_Splice_Rec_996755,Human_Splice_Rec_996760,Human_Splice_Rec_996761,Human_Splice_Rec_996766,Human_Splice_Rec_996767,Human_Splice_Rec_996772,Human_Splice_Rec_996773,Human_Splice_Rec_996778,Human_Splice_Rec_996779,Human_Splice_Rec_996784,Human_Splice_Rec_996785,Human_Splice_Rec_996790,Human_Splice_Rec_996791,Human_Splice_Rec_996796 RMVar_hsa_circ_61370,RMVar_hsa_circ_274598,RMVar_hsa_circ_253478,RMVar_hsa_circ_315033 109414 RMVar_ID_109414 Human_SNP_ID_375004740 m1A Human chr8 - 99892049 99892049 99892049 ACTTAATCATATTTTCTGAATCTCTTAAGGTTAGCATACGTATCAAGGACAGTAACTACCATGGC ACTTAATCATATTTTCTGAATCTCTTAAGGTTGGCATACGTATCAAGGACAGTAACTACCATGGC T C COX6C Ensembl:ENSG00000164919 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:99892026..99892075 26863196 MeRIP-seq:(Medium) rs1130474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995649,Human_RBP_ID_5328881,Human_RBP_ID_9338316,Human_RBP_ID_16297302,Human_RBP_ID_22464978,Human_RBP_ID_23216163 Human_Splice_Rec_996736,Human_Splice_Rec_996744,Human_Splice_Rec_996752,Human_Splice_Rec_996764,Human_Splice_Rec_996776,Human_Splice_Rec_996782,Human_Splice_Rec_996788,Human_Splice_Rec_996794 RMVar_hsa_circ_61370,RMVar_hsa_circ_315033 109415 RMVar_ID_109415 Human_SNP_ID_375004741 m1A Human chr8 - 99892049 99892049 99892049 ACTTAATCATATTTTCTGAATCTCTTAAGGTTAGCATACGTATCAAGGACAGTAACTACCATGGC ACTTAATCATATTTTCTGAATCTCTTAAGGTTCGCATACGTATCAAGGACAGTAACTACCATGGC T G COX6C Ensembl:ENSG00000164919 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:99892026..99892075 26863196 MeRIP-seq:(Medium) rs1130474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995649,Human_RBP_ID_5328881,Human_RBP_ID_9338316,Human_RBP_ID_16297302,Human_RBP_ID_22464978,Human_RBP_ID_23216163 Human_Splice_Rec_996736,Human_Splice_Rec_996744,Human_Splice_Rec_996752,Human_Splice_Rec_996764,Human_Splice_Rec_996776,Human_Splice_Rec_996782,Human_Splice_Rec_996788,Human_Splice_Rec_996794 RMVar_hsa_circ_61370,RMVar_hsa_circ_315033 109416 RMVar_ID_109416 Human_SNP_ID_375066964 m1A Human chr8 - 100150711 100150711 100150711 TCCACCACAAACCCCAACCCGCCAATTCGCTTACCTACACAGCACGGAAAAACTCACTCCGCGTT TCCACCACAAACCCCAACCCGCCAATTCGCTTTCCTACACAGCACGGAAAAACTCACTCCGCGTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:100150683..100150778 26863196 MeRIP-seq:(Medium) rs113946813 Functional Loss SNV dbSNP153 33..33 33 - - - 109417 RMVar_ID_109417 Human_SNP_ID_375066965 m1A Human chr8 - 100150711 100150711 100150711 TCCACCACAAACCCCAACCCGCCAATTCGCTTACCTACACAGCACGGAAAAACTCACTCCGCGTT TCCACCACAAACCCCAACCCGCCAATTCGCTTCCCTACACAGCACGGAAAAACTCACTCCGCGTT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:100150683..100150778 26863196 MeRIP-seq:(Medium) rs113946813 Functional Loss SNV dbSNP153 33..33 33 - - - 109418 RMVar_ID_109418 Human_SNP_ID_375076735 m1A Human chr8 + 100194261 100194261 100194261 AAAAGCGGAAGAAAACATGAAGATGGCGGTGGAGATAAGAGTAAAATATTTTTTCTATTTAGGTT AAAAGCGGAAGAAAACATGAAGATGGCGGTGGGGATAAGAGTAAAATATTTTTTCTATTTAGGTT A G SPAG1 Ensembl:ENSG00000104450 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:100194211..100194341 26863196 MeRIP-seq:(Medium) rs199651642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_997225,Human_Splice_Rec_997277 RMVar_hsa_circ_8458,RMVar_hsa_circ_26952,RMVar_hsa_circ_36789,RMVar_hsa_circ_61172,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114 109419 RMVar_ID_109419 Human_SNP_ID_375080971 m1A Human chr8 + 100213207 100213207 100213207 AGGCGGCAAGCGGCCGGCAAGGGGCGCGCCGCAGCGGGGCCAGACCCCGGAGGCCGGCGCGGACA AGGCGGCAAGCGGCCGGCAAGGGGCGCGCCGCCGCGGGGCCAGACCCCGGAGGCCGGCGCGGACA A C SPAG1 Ensembl:ENSG00000104450 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:100213054..100213365;chr8:100213051..100213366;chr8:100213071..100213374 26863196 MeRIP-seq:(Medium) rs1305186541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_36789,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_5084,RMVar_hsa_circ_253489 109420 RMVar_ID_109420 Human_SNP_ID_375091617 m1A Human chr8 - 100259122 100259122 100259122 GTGCCACCCGAAGTCATGCTGGCGGTTCATCCAGTGGCTTGCCTGAAGGTAAATCTAGTGCCACC GTGCCACCCGAAGTCATGCTGGCGGTTCATCCGGTGGCTTGCCTGAAGGTAAATCTAGTGCCACC T C RNF19A Ensembl:ENSG00000034677 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:100259074..100259164 32194978 MeRIP-seq:(Medium) rs1397005995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253500,RMVar_hsa_circ_269789,RMVar_hsa_circ_253502,RMVar_hsa_circ_269719,RMVar_hsa_circ_253501,RMVar_hsa_circ_253498,RMVar_hsa_circ_253499 109421 RMVar_ID_109421 Human_SNP_ID_375110073 m1A Human chr8 - 100336388 100336384 100336388 GTCAGTGTCGTTCGGTTTCTGGGCTTGCCCCTAACTGACTTCCTCGTCCTTTCTTTGGAATTTGC GTCAGTGTCGTTCGGTTTCTGGGCTTGCCCCT____GACTTCCTCGTCCTTTCTTTGGAATTTGC CAGTT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:100336337..100336436 26863196 MeRIP-seq:(Medium) rs1459151954 Functional Loss DEL dbSNP153 33..36 33 - - - 109422 RMVar_ID_109422 Human_SNP_ID_375111233 m1A Human chr8 + 100341816 100341816 100341816 TATGACTCCAATGAAAAGGGCTGAGAGGGGAGAGCTGCGGTTCAGCACAGAGACGAAAAGTCAGA TATGACTCCAATGAAAAGGGCTGAGAGGGGAGCGCTGCGGTTCAGCACAGAGACGAAAAGTCAGA A C AP001574.1 Ensembl:ENSG00000253217 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:100341802..100341902 26863196 MeRIP-seq:(Medium) rs993621860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5630590 109423 RMVar_ID_109423 Human_SNP_ID_375120432 m1A Human chr8 + 100381748 100381748 100381748 AGTCTGGGTTGGAGGAGAGCTACAGGCAGATCAGGAACACCCATCTTGGATTTGACCTGAGTGAA AGTCTGGGTTGGAGGAGAGCTACAGGCAGATCTGGAACACCCATCTTGGATTTGACCTGAGTGAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:100381686..100381771 26863196 MeRIP-seq:(Medium) rs949971163 Functional Loss SNV dbSNP153 33..33 33 - - - 109424 RMVar_ID_109424 Human_SNP_ID_375129791 m1A Human chr8 - 100421057 100421057 100421057 CCTCCATGACGACGCTACCAAAAATCACATATACCTCCAGTCACTCTCTCCACCCTTACCCGGCC CCTCCATGACGACGCTACCAAAAATCACATATGCCTCCAGTCACTCTCTCCACCCTTACCCGGCC T C AP003472.1 Ensembl:ENSG00000253824 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:100421008..100421184 26863196 MeRIP-seq:(Medium) rs1489398169 Functional Loss SNV dbSNP153 33..33 33 - - - 109425 RMVar_ID_109425 Human_SNP_ID_375130479 m1A Human chr8 - 100424110 100424110 100424110 TCAGACATCACCTTTTCCTCAGTGCCCTCCCTAGTTCTCTACCTAAAACCACACACTCCCCTCCC TCAGACATCACCTTTTCCTCAGTGCCCTCCCTGGTTCTCTACCTAAAACCACACACTCCCCTCCC T C AP003472.1 Ensembl:ENSG00000253824 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:100424061..100424221 26863196 MeRIP-seq:(Medium) rs1490270781 Functional Loss SNV dbSNP153 33..33 33 - - - 109426 RMVar_ID_109426 Human_SNP_ID_375198001 m1A Human chr8 - 100703072 100703072 100703072 GACCCTGGGAAAAAGAATTTTCAGCAAAGTACAAAAATTTAAAGCATTCCTTTCTTTAATTTTGT GACCCTGGGAAAAAGAATTTTCAGCAAAGTACGAAAATTTAAAGCATTCCTTTCTTTAATTTTGT T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs556768806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691892,Human_RBP_ID_4966742,Human_RBP_ID_22408709,Human_RBP_ID_23088229,Human_RBP_ID_26552637 Human_miRNA_ID_187255 RMVar_hsa_circ_253522,RMVar_hsa_circ_89246,RMVar_hsa_circ_85536,RMVar_hsa_circ_253523 109427 RMVar_ID_109427 Human_SNP_ID_375198098 m1A Human chr8 - 100703279 100703279 100703279 ATCTAAACATCGAAAAACTTAAATATTATGGAAAAAAAACATTGCAAAATATAAAATAAATAAAA ATCTAAACATCGAAAAACTTAAATATTATGGAGAAAAAACATTGCAAAATATAAAATAAATAAAA T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:100703228..100704131 32194978 MeRIP-seq:(Medium) rs1383281924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87906,Human_RBP_ID_691892,Human_RBP_ID_1691712,Human_RBP_ID_2050650,Human_RBP_ID_3127931,Human_RBP_ID_3869169,Human_RBP_ID_5123638,Human_RBP_ID_5154075,Human_RBP_ID_8676337,Human_RBP_ID_9218204,Human_RBP_ID_17543899,Human_RBP_ID_17665825,Human_RBP_ID_18196734,Human_RBP_ID_21563084,Human_RBP_ID_22516454,Human_RBP_ID_23082043,Human_RBP_ID_24518161,Human_RBP_ID_26189731,Human_RBP_ID_26552647,Human_RBP_ID_27119337 Human_Splice_Rec_997592,Human_Splice_Rec_997620,Human_Splice_Rec_997650,Human_Splice_Rec_997680,Human_Splice_Rec_997692,Human_Splice_Rec_997700 Human_miRNA_ID_2645070 RMVar_hsa_circ_253522,RMVar_hsa_circ_89246,RMVar_hsa_circ_85536,RMVar_hsa_circ_253523 109428 RMVar_ID_109428 Human_SNP_ID_375198651 m1A Human chr8 + 100704965 100704965 100704965 CGGAGTGACTCTGGAGACTCGAGCATATGAAGAAGTTCTGAATTATCAATCTCCAACAACATGCC CGGAGTGACTCTGGAGACTCGAGCATATGAAGTAGTTCTGAATTATCAATCTCCAACAACATGCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:100704378..100705594 32194978 MeRIP-seq:(Medium) rs1284429123 Functional Loss SNV dbSNP153 33..33 33 - - - 109429 RMVar_ID_109429 Human_SNP_ID_375199290 m1A Human chr8 + 100706985 100706985 100706985 GTCTAGGAGCAGCTGGGCGGATAGCACCGGGCATATTTTGGAATGCTGCATTTTAAAGATGTGAA GTCTAGGAGCAGCTGGGCGGATAGCACCGGGCGTATTTTGGAATGCTGCATTTTAAAGATGTGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr8:100706673..100707036;chr8:100706976..100707000 26863196 MeRIP-seq:(Medium) rs1342809737 Functional Loss SNV dbSNP153 33..33 33 - - - 109430 RMVar_ID_109430 Human_SNP_ID_375203939 m1A Human chr8 - 100721393 100721393 100721393 CTACGCGTATGTGAACTTCCAGCAGCCGGCGGACGGTGAGCGCCGGGCTCCGCGGTCGGCCGGGC CTACGCGTATGTGAACTTCCAGCAGCCGGCGGCCGGTGAGCGCCGGGCTCCGCGGTCGGCCGGGC T G PABPC1 Ensembl:ENSG00000070756 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:100718114..100722017 32194978 MeRIP-seq:(Medium) rs1214378887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795316,Human_RBP_ID_844754,Human_RBP_ID_1053828,Human_RBP_ID_5628322,Human_RBP_ID_16300215,Human_RBP_ID_18196509,Human_RBP_ID_18452089,Human_RBP_ID_26832336,Human_RBP_ID_27119383 Human_Splice_Rec_997593,Human_Splice_Rec_997622,Human_Splice_Rec_997623,Human_Splice_Rec_997653,Human_Splice_Rec_997709,Human_Splice_Rec_997777,Human_Splice_Rec_997783,Human_Splice_Rec_997792,Human_Splice_Rec_997793,Human_Splice_Rec_997801,Human_Splice_Rec_997805,Human_Splice_Rec_997809 RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_253549 109431 RMVar_ID_109431 Human_SNP_ID_375203982 m1A Human chr8 - 100721583 100721583 100721583 CGGCCTGTGGCCCTGCGGGCAGCCGTGCCGAGATGAACCCCAGTGCCCCCAGCTACCCCATGGCC CGGCCTGTGGCCCTGCGGGCAGCCGTGCCGAGGTGAACCCCAGTGCCCCCAGCTACCCCATGGCC T C PABPC1 Ensembl:ENSG00000070756 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:100721535..100721824 26863196 MeRIP-seq:(Medium) rs1243077943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691985,Human_RBP_ID_795228,Human_RBP_ID_8676412,Human_RBP_ID_16300227,Human_RBP_ID_17433955,Human_RBP_ID_17543954,Human_RBP_ID_18889198,Human_RBP_ID_18961602,Human_RBP_ID_22534381,Human_RBP_ID_26141203,Human_RBP_ID_26552678,Human_RBP_ID_27119386 Human_Splice_Rec_997652,Human_Splice_Rec_997800,Human_Splice_Rec_997804,Human_Splice_Rec_997814 RMVar_hsa_circ_98534,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_253549 109432 RMVar_ID_109432 Human_SNP_ID_375204084 m1A Human chr8 - 100721794 100721794 100721794 AGGCCTTCCCGCTGCCCGGACCCGACACCGCCACCCTCGCTCCCCGCCGGCAGCCGGCAGCCAGC AGGCCTTCCCGCTGCCCGGACCCGACACCGCCCCCCTCGCTCCCCGCCGGCAGCCGGCAGCCAGC T G PABPC1 Ensembl:ENSG00000070756 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:100721462..100722100 26863196 MeRIP-seq:(Medium) rs1031712725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254710,Human_RBP_ID_691985,Human_RBP_ID_795318,Human_RBP_ID_844756,Human_RBP_ID_4996944,Human_RBP_ID_5480454,Human_RBP_ID_8676416,Human_RBP_ID_9218231,Human_RBP_ID_17433959,Human_RBP_ID_17543962,Human_RBP_ID_18889200,Human_RBP_ID_18961612,Human_RBP_ID_22408729,Human_RBP_ID_22534383,Human_RBP_ID_24237957,Human_RBP_ID_24518196,Human_RBP_ID_26558884,Human_RBP_ID_27569540 Human_Splice_Rec_997621,Human_Splice_Rec_997651,Human_Splice_Rec_997791,Human_Splice_Rec_997798,Human_Splice_Rec_997799,Human_Splice_Rec_997803,Human_Splice_Rec_997808,Human_Splice_Rec_997812,Human_Splice_Rec_997813,Human_Splice_Rec_997816,Human_Splice_Rec_997818 Human_miRNA_ID_2146516,Human_miRNA_ID_2987941,Human_miRNA_ID_3021639 RMVar_hsa_circ_98534,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_253547 109433 RMVar_ID_109433 Human_SNP_ID_375204103 m1A Human chr8 - 100721855 100721855 100721855 GCCGAGACCGACCCGCCCGCCCGCGGCCCCGCAGCAGCTCCAAGAAGGAACCAAGAGACCGAGGC GCCGAGACCGACCCGCCCGCCCGCGGCCCCGCCGCAGCTCCAAGAAGGAACCAAGAGACCGAGGC T G PABPC1 Ensembl:ENSG00000070756 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:100721818..100722017 32194978 MeRIP-seq:(Medium) rs1174060448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_691985,Human_RBP_ID_795319,Human_RBP_ID_844757,Human_RBP_ID_960530,Human_RBP_ID_4996946,Human_RBP_ID_5123640,Human_RBP_ID_5153907,Human_RBP_ID_17433961,Human_RBP_ID_17543963,Human_RBP_ID_17666162,Human_RBP_ID_18196516,Human_RBP_ID_21563103,Human_RBP_ID_24441529,Human_RBP_ID_26558885 Human_Splice_Rec_997798,Human_Splice_Rec_997808,Human_Splice_Rec_997812,Human_Splice_Rec_997816,Human_Splice_Rec_997818 Human_miRNA_ID_2615183,Human_miRNA_ID_3065746 RMVar_hsa_circ_98534,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_253547 109434 RMVar_ID_109434 Human_SNP_ID_375253801 m1A Human chr8 + 100919426 100919426 100919426 CATATGCCAAAATTTTAAATGGAACACACTACATTTTTTTCTAATCAATCCCCCCCTCTCCCAGA CATATGCCAAAATTTTAAATGGAACACACTACGTTTTTTTCTAATCAATCCCCCCCTCTCCCAGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:100919376..100919450 32194978 MeRIP-seq:(Medium) rs985513748 Functional Loss SNV dbSNP153 33..33 33 - - - 109435 RMVar_ID_109435 Human_SNP_ID_375253802 m1A Human chr8 - 100919427 100919426 100919427 TTCTGGGAGAGGGGGGGATTGATTAGAAAAAAATGTAGTGTGTTCCATTTAAAATTTTGGCATAT TTCTGGGAGAGGGGGGGATTGATTAGAAAAAA_TGTAGTGTGTTCCATTTAAAATTTTGGCATAT AT A YWHAZ Ensembl:ENSG00000164924 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:100919376..100919450 32194978 MeRIP-seq:(Medium) rs1306793228 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_692051,Human_RBP_ID_796425,Human_RBP_ID_2050717,Human_RBP_ID_3128133,Human_RBP_ID_3869234,Human_RBP_ID_7792772,Human_RBP_ID_8221974,Human_RBP_ID_17433962,Human_RBP_ID_18386241,Human_RBP_ID_22408741,Human_RBP_ID_23082093,Human_RBP_ID_24238007,Human_RBP_ID_24518218,Human_RBP_ID_26558248,Human_RBP_ID_27119404,Human_RBP_ID_27772489 109436 RMVar_ID_109436 Human_SNP_ID_375261737 m1A Human chr8 - 100948617 100948617 100948617 GAATACAGAGAGAAAATTGAGACGGAGCTAAGAGATATCTGCAATGATGTACTGGTGAGAATCAA GAATACAGAGAGAAAATTGAGACGGAGCTAAGTGATATCTGCAATGATGTACTGGTGAGAATCAA T A YWHAZ Ensembl:ENSG00000164924 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1563691443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628323,Human_RBP_ID_18124709,Human_RBP_ID_19141542 Human_Splice_Rec_997821,Human_Splice_Rec_997833,Human_Splice_Rec_997843,Human_Splice_Rec_997853,Human_Splice_Rec_997863,Human_Splice_Rec_997907,Human_Splice_Rec_997917,Human_Splice_Rec_997927,Human_Splice_Rec_997937,Human_Splice_Rec_997945,Human_Splice_Rec_997955,Human_Splice_Rec_997963,Human_Splice_Rec_997969,Human_Splice_Rec_997975 RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 109437 RMVar_ID_109437 Human_SNP_ID_375262551 m1A Human chr8 + 100950917 100950917 100950917 ACCAGCGGCTATGCTCAGGCTCACCCGCCCCCAAAGCAGGATATGCGTCCCCAAACCGAGCGCAG ACCAGCGGCTATGCTCAGGCTCACCCGCCCCCTAAGCAGGATATGCGTCCCCAAACCGAGCGCAG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:100950876..100951150 26863196 MeRIP-seq:(Medium) rs73697346 Functional Loss SNV dbSNP153 33..33 33 - - - 109438 RMVar_ID_109438 Human_SNP_ID_375263038 m1A Human chr8 - 100951978 100951978 100951978 CAGCCTCGCCGCTGCTGCCGCCGCCGCCGCCCAGAGACTGCTGAGCCCGTCCGTCCGCCGCCACC CAGCCTCGCCGCTGCTGCCGCCGCCGCCGCCCGGAGACTGCTGAGCCCGTCCGTCCGCCGCCACC T C YWHAZ Ensembl:ENSG00000164924 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:100951315..100952000;chr8:100950708..100952549;chr8:100950709..100953338;chr8:100950732..100952944 26863196 MeRIP-seq:(Medium) rs1256278636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255001,Human_RBP_ID_692101,Human_RBP_ID_795896,Human_RBP_ID_4995659,Human_RBP_ID_5514032,Human_RBP_ID_9338325,Human_RBP_ID_16301654,Human_RBP_ID_18889240,Human_RBP_ID_22534413,Human_RBP_ID_27119433,Human_RBP_ID_27361616 Human_Splice_Rec_997819,Human_Splice_Rec_997831,Human_Splice_Rec_997887,Human_Splice_Rec_997953,Human_Splice_Rec_997977,Human_Splice_Rec_997981,Human_Splice_Rec_997985,Human_Splice_Rec_997989 Human_miRNA_ID_2269258,Human_miRNA_ID_2424101,Human_miRNA_ID_2433761 RMVar_hsa_circ_126272,RMVar_hsa_circ_253562 109439 RMVar_ID_109439 Human_SNP_ID_375263622 m1A Human chr8 + 100953335 100953335 100953335 TCGTAGTCCCCAGGGTTCCAGCTGGCGGTGGGAGTGGGCCACAGGCCGGGTGATGAGCCGGGACG TCGTAGTCCCCAGGGTTCCAGCTGGCGGTGGGGGTGGGCCACAGGCCGGGTGATGAGCCGGGACG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:100953027..100953348 26863196 MeRIP-seq:(Medium) rs558446089 Functional Loss SNV dbSNP153 33..33 33 - - - 109440 RMVar_ID_109440 Human_SNP_ID_375282097 m1A Human chr8 - 101027365 101027365 101027365 GAGTAGGGGCAGCACCCAGTTCTGATTCAGCCATCCAGACACAGCCGAGTGGTCTCAGGGCAGGT GAGTAGGGGCAGCACCCAGTTCTGATTCAGCCGTCCAGACACAGCCGAGTGGTCTCAGGGCAGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:101027323..101027454 26863196 MeRIP-seq:(Medium) rs1402298039 Functional Loss SNV dbSNP153 33..33 33 - - - 109441 RMVar_ID_109441 Human_SNP_ID_375325102 m1A Human chr8 + 101201714 101201711 101201714 TCCAGCTTGCTTTTTGGCATTTTTCTGCTGAGACTGAATTTTCTGCTGTCCACGAGCCATATCTA TCCAGCTTGCTTTTTGGCATTTTTCTGCTG___CTGAATTTTCTGCTGTCCACGAGCCATATCTA GAGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:101201651..101202421 26863196 MeRIP-seq:(Medium) rs764936865 Functional Loss DEL dbSNP153 31..33 33 - - - 109442 RMVar_ID_109442 Human_SNP_ID_375325106 m1A Human chr8 + 101201714 101201714 101201714 TCCAGCTTGCTTTTTGGCATTTTTCTGCTGAGACTGAATTTTCTGCTGTCCACGAGCCATATCTA TCCAGCTTGCTTTTTGGCATTTTTCTGCTGAGTCTGAATTTTCTGCTGTCCACGAGCCATATCTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:101201651..101202421 26863196 MeRIP-seq:(Medium) rs769017236 Functional Loss SNV dbSNP153 33..33 33 - - - 109443 RMVar_ID_109443 Human_SNP_ID_375325895 m1A Human chr8 - 101204889 101204889 101204889 CCAAAACGATGGTGTTAAAAGCTAGGGTCAGGATGTGGAGCGCTGCCTGGGCCTCTTCCTTTCCG CCAAAACGATGGTGTTAAAAGCTAGGGTCAGGTTGTGGAGCGCTGCCTGGGCCTCTTCCTTTCCG T A ZNF706 Ensembl:ENSG00000120963 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:101204882..101205304 26863196 MeRIP-seq:(Medium) rs558327902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5090860,Human_RBP_ID_5224419,Human_RBP_ID_5329178,Human_RBP_ID_8154735,Human_RBP_ID_16302562,Human_RBP_ID_17173522,Human_RBP_ID_18505674,Human_RBP_ID_21995088,Human_RBP_ID_22484014,Human_RBP_ID_24441820 109444 RMVar_ID_109444 Human_SNP_ID_375326108 m1A Human chr8 + 101205566 101205566 101205566 TGGGCCTCCTCCACCCGCTCAGGAGGGGAAACACGAGAGCCGGGAGCACAACAGCCTCGCACGCC TGGGCCTCCTCCACCCGCTCAGGAGGGGAAACGCGAGAGCCGGGAGCACAACAGCCTCGCACGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr8:101205263..101205700;chr8:101205426..101205675 26863196 MeRIP-seq:(Medium) rs910924887 Functional Loss SNV dbSNP153 33..33 33 - - - 109445 RMVar_ID_109445 Human_SNP_ID_375326121 m1A Human chr8 + 101205578 101205578 101205578 ACCCGCTCAGGAGGGGAAACACGAGAGCCGGGAGCACAACAGCCTCGCACGCCCGCCGCCGCCGC ACCCGCTCAGGAGGGGAAACACGAGAGCCGGGGGCACAACAGCCTCGCACGCCCGCCGCCGCCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:101205267..101205712;chr8:101205426..101205640;chr8:101204817..101205893;chr8:101204867..101205725;chr8:101205389..101205708 26863196 MeRIP-seq:(Medium) rs1056322938 Functional Loss SNV dbSNP153 33..33 33 - - - 109446 RMVar_ID_109446 Human_SNP_ID_375616005 m1A Human chr8 - 102400328 102400328 102400328 GTTATAGATTAGCGAGCTCAGGGAGTGGCATCAGGTGGGTATGCCATGTATTGTTTTTCTACCTT GTTATAGATTAGCGAGCTCAGGGAGTGGCATCCGGTGGGTATGCCATGTATTGTTTTTCTACCTT T G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:102400325..102400393 26863196 MeRIP-seq:(Medium) rs1027616848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16306119 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 109447 RMVar_ID_109447 Human_SNP_ID_375618687 m1A Human chr8 - 102411322 102411322 102411322 CTAATGATAGTGTTTTCCTGAGTTGTAATTTGACAGCTGAAAACCGTGCGTAGAGTGTCAAAGGA CTAATGATAGTGTTTTCCTGAGTTGTAATTTGGCAGCTGAAAACCGTGCGTAGAGTGTCAAAGGA T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:102411316..102411435 32194978 MeRIP-seq:(Medium) rs1203708385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16306645,Human_RBP_ID_22704433,Human_RBP_ID_24391065 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 109448 RMVar_ID_109448 Human_SNP_ID_375619054 m1A Human chr8 - 102412240 102412240 102412240 GGGGCCGCCCTCGAGTGGAGGACGAGAAGGAAAGCACCATGACGTCCATCCATTTCGTGGTTCAC GGGGCCGCCCTCGAGTGGAGGACGAGAAGGAAGGCACCATGACGTCCATCCATTTCGTGGTTCAC T C UBR5 Ensembl:ENSG00000104517 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:102412189..102412287;chr8:102412142..102412253 26863196 MeRIP-seq:(Medium) rs376765196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3887937,Human_RBP_ID_3973301,Human_RBP_ID_4996273,Human_RBP_ID_8222402,Human_RBP_ID_8944469,Human_RBP_ID_9440915,Human_RBP_ID_18466798,Human_RBP_ID_18472621,Human_RBP_ID_22465939,Human_RBP_ID_26795110 Human_Splice_Rec_998529,Human_Splice_Rec_998641,Human_Splice_Rec_998785 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 109449 RMVar_ID_109449 Human_SNP_ID_375619206 m1A Human chr8 + 102412640 102412640 102412640 GGTCCGGACTAGGGGAGGTGAGGAAGGAGGGGAAGGAGATGAGCCCGCACCGCGCGTCACTAGCG GGTCCGGACTAGGGGAGGTGAGGAAGGAGGGGGAGGAGATGAGCCCGCACCGCGCGTCACTAGCG A G RF00017-4497 RNACentral:URS000098F9B6 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:102412590..102412706 26863196 MeRIP-seq:(Medium) rs889544432 Functional Loss SNV dbSNP153 33..33 33 - - - 109450 RMVar_ID_109450 Human_SNP_ID_375619216 m1A Human chr8 - 102412668 102412668 102412668 AGAAGTGAAGATGGCGGCGGCAGCTTCTCGCTAGTGACGCGCGGTGCGGGCTCATCTCCTTCCCC AGAAGTGAAGATGGCGGCGGCAGCTTCTCGCTGGTGACGCGCGGTGCGGGCTCATCTCCTTCCCC T C UBR5 Ensembl:ENSG00000104517 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:102412410..102412702 26863196 MeRIP-seq:(Medium) rs1298438821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88225,Human_RBP_ID_4967261,Human_RBP_ID_5514057,Human_RBP_ID_16306655,Human_RBP_ID_22626766,Human_RBP_ID_27119586 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 109451 RMVar_ID_109451 Human_SNP_ID_375619219 m1A Human chr8 + 102412675 102412675 102412675 GAGATGAGCCCGCACCGCGCGTCACTAGCGAGAAGCTGCCGCCGCCATCTTCACTTCTGCCCCAG GAGATGAGCCCGCACCGCGCGTCACTAGCGAGGAGCTGCCGCCGCCATCTTCACTTCTGCCCCAG A G RF00017-4497 RNACentral:URS000098F9B6 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:102412547..102412710 26863196 MeRIP-seq:(Medium) rs1358456351 Functional Loss SNV dbSNP153 33..33 33 - - - 109452 RMVar_ID_109452 Human_SNP_ID_375678638 m1A Human chr8 - 102651391 102651391 102651391 CCCTGTTGTGTTCATGGGCACACAAGTCCCCAAAGGCGCTGTCATGTTTGTGGTACCCCAGCCCG CCCTGTTGTGTTCATGGGCACACAAGTCCCCAGAGGCGCTGTCATGTTTGTGGTACCCCAGCCCG T C KLF10 Ensembl:ENSG00000155090 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:102651340..102651413 26863196 MeRIP-seq:(Medium) rs148650585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796836,Human_RBP_ID_17433972,Human_RBP_ID_22115097,Human_RBP_ID_24537194,Human_RBP_ID_27569555 109453 RMVar_ID_109453 Human_SNP_ID_375680053 m1A Human chr8 - 102655093 102655093 102655093 ACGCGAGCCAGGGGAGGAAGGGGCTGCTCGCAAGCACTCGGGAGGCGGGGTGTCCACAGGAGAGG ACGCGAGCCAGGGGAGGAAGGGGCTGCTCGCATGCACTCGGGAGGCGGGGTGTCCACAGGAGAGG T A KLF10 Ensembl:ENSG00000155090 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:102655090..102655173 26863196 MeRIP-seq:(Medium) rs1292445002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3885362,Human_RBP_ID_8238829 109454 RMVar_ID_109454 Human_SNP_ID_375680105 m1A Human chr8 - 102655267 102655267 102655267 CGCATGGAGACCCGAGAGGGCTGGTGAGGAGGAGGATGACGAGCGGGGGAGGAGTGGGGAGGGGG CGCATGGAGACCCGAGAGGGCTGGTGAGGAGGCGGATGACGAGCGGGGGAGGAGTGGGGAGGGGG T G KLF10 Ensembl:ENSG00000155090 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:102655264..102655457 26863196 MeRIP-seq:(Medium) rs1277936773 Functional Loss SNV dbSNP153 33..33 33 - - - 109455 RMVar_ID_109455 Human_SNP_ID_375717907 m1A Human chr8 + 102810962 102810962 102810962 CGTGGCCGGGGATGCCGCGAGGCCGCGCCTCCAGGGCTGTGCGCGGGCGGGTGTTGCTGGGGAGA CGTGGCCGGGGATGCCGCGAGGCCGCGCCTCCTGGGCTGTGCGCGGGCGGGTGTTGCTGGGGAGA A T RF00017-1264,RF00017-4572,GASAL1,GASAL1:2,GASAL1:3,GASAL1:4,RF00017-4498,GASAL1:5,GASAL1:6,GASAL1:7,GASAL1:8 RNACentral:URS00009A773B,RNACentral:URS000099187D,RNACentral:URS0000D57889,RNACentral:URS0000BC44C1,RNACentral:URS0000D5829A,RNACentral:URS0000D5DF71,RNACentral:URS0000930330,RNACentral:URS0000D5A496,RNACentral:URS0000D5DF3F,RNACentral:URS0000D5A727,RNACentral:URS0000D59898 SRP RNA,SRP RNA,lincRNA,lincRNA,lincRNA,lincRNA,SRP RNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron,exon,intron,intron,intron,exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:102810858..102811078 26863196 MeRIP-seq:(Medium) rs1250373268 Functional Loss SNV dbSNP153 33..33 33 - - - 109456 RMVar_ID_109456 Human_SNP_ID_375731252 m1A Human chr8 - 102864051 102864051 102864051 TCGCTCTGCTGCTCTGCAGTGTGACGAGTCCGAATCCTCTTCCCACCCAGCCCGCGCCTTTCTTC TCGCTCTGCTGCTCTGCAGTGTGACGAGTCCGCATCCTCTTCCCACCCAGCCCGCGCCTTTCTTC T G AZIN1 Ensembl:ENSG00000155096 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cells, overexperss TRMT6;HEK293T,Wild Type chr8:102863949..102864139 29072297,26863410 m1A-MAP:(High) rs1235984921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_692483,Human_RBP_ID_4996278,Human_RBP_ID_5452901,Human_RBP_ID_5514072,Human_RBP_ID_9338340,Human_RBP_ID_18889501,Human_RBP_ID_21654289,Human_RBP_ID_26189931,Human_RBP_ID_26552903,Human_RBP_ID_27535254 RMVar_hsa_circ_124698,RMVar_hsa_circ_253735 109457 RMVar_ID_109457 Human_SNP_ID_375731448 m1A Human chr8 + 102864398 102864398 102864398 GGCCGGTCGCTTCCCGCCCTCCAGCCACCCGCAGCTCCCCGGCAGGCGAAGGGCGGCCGCGCGGG GGCCGGTCGCTTCCCGCCCTCCAGCCACCCGCCGCTCCCCGGCAGGCGAAGGGCGGCCGCGCGGG A C AZIN1-AS1 Ensembl:ENSG00000253320 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:102864347..102864423 26863196 MeRIP-seq:(Medium) rs937081156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996790,Human_RBP_ID_5633348 109458 RMVar_ID_109458 Human_SNP_ID_375731464 m1A Human chr8 - 102864433 102864433 102864433 GCTCCAGCCGAGCCGCCTCCCTCTCTCGGCCCACACCCGCGCGGCCGCCCTTCGCCTGCCGGGGA GCTCCAGCCGAGCCGCCTCCCTCTCTCGGCCCGCACCCGCGCGGCCGCCCTTCGCCTGCCGGGGA T C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:102864382..102864471 26863196 MeRIP-seq:(Medium) rs1055552728 Functional Loss SNV dbSNP153 33..33 33 - - - 109459 RMVar_ID_109459 Human_SNP_ID_375731939 m1A Human chr8 + 102865834 102865834 102865834 TCCAGGCAAGGGAAACGGATGAGAGAAGGCACAGAAGTGGGTGGGTTTAGAGAATTGTGAATAGC TCCAGGCAAGGGAAACGGATGAGAGAAGGCACGGAAGTGGGTGGGTTTAGAGAATTGTGAATAGC A G AZIN1-AS1 Ensembl:ENSG00000253320 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:102865757..102865933 26863196 MeRIP-seq:(Medium) rs771352218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5631402 109460 RMVar_ID_109460 Human_SNP_ID_375769274 m1A Human chr8 + 103021151 103021151 103021151 CGGAGCTTAGGTCGGGAAGGGATGGATCGCTGAGCCGATAGCGTCCGCTAGGCTGTCTGCCTCGG CGGAGCTTAGGTCGGGAAGGGATGGATCGCTGGGCCGATAGCGTCCGCTAGGCTGTCTGCCTCGG A G ATP6V1C1 Ensembl:ENSG00000155097 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103021101..103021225 26863196 MeRIP-seq:(Medium) rs570843340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995667,Human_RBP_ID_7794588,Human_RBP_ID_18426734 Human_Splice_Rec_999145,Human_Splice_Rec_999165,Human_Splice_Rec_999189,Human_Splice_Rec_999213 109461 RMVar_ID_109461 Human_SNP_ID_375769275 m1A Human chr8 + 103021151 103021151 103021151 CGGAGCTTAGGTCGGGAAGGGATGGATCGCTGAGCCGATAGCGTCCGCTAGGCTGTCTGCCTCGG CGGAGCTTAGGTCGGGAAGGGATGGATCGCTGTGCCGATAGCGTCCGCTAGGCTGTCTGCCTCGG A T ATP6V1C1 Ensembl:ENSG00000155097 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103021101..103021225 26863196 MeRIP-seq:(Medium) rs570843340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995667,Human_RBP_ID_7794588,Human_RBP_ID_18426734 Human_Splice_Rec_999145,Human_Splice_Rec_999165,Human_Splice_Rec_999189,Human_Splice_Rec_999213 109462 RMVar_ID_109462 Human_SNP_ID_375769287 m1A Human chr8 + 103021168 103021168 103021168 AGGGATGGATCGCTGAGCCGATAGCGTCCGCTAGGCTGTCTGCCTCGGTACCTGTTACTGCTGCT AGGGATGGATCGCTGAGCCGATAGCGTCCGCTGGGCTGTCTGCCTCGGTACCTGTTACTGCTGCT A G ATP6V1C1 Ensembl:ENSG00000155097 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:103021118..103021208 26863196 MeRIP-seq:(Medium) rs973313183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995667,Human_RBP_ID_5480481,Human_RBP_ID_18426734 Human_Splice_Rec_999145,Human_Splice_Rec_999165,Human_Splice_Rec_999189,Human_Splice_Rec_999213 109463 RMVar_ID_109463 Human_SNP_ID_375769317 m1A Human chr8 - 103021296 103021296 103021296 TCTCTGCCCCCGCACCCACCCGCGTCCCTCCCAGGCAGCGACCGGAGCTCATGCTTCGGCCTGAC TCTCTGCCCCCGCACCCACCCGCGTCCCTCCCGGGCAGCGACCGGAGCTCATGCTTCGGCCTGAC T C AP003550.1 Ensembl:ENSG00000254236 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103021292..103021596 26863196 MeRIP-seq:(Medium) rs1354623102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253748 109464 RMVar_ID_109464 Human_SNP_ID_375833642 m1A Human chr8 - 103298923 103298923 103298923 GTCTAACCCACCGTTCCCCCCAGGGACCTGAGACGGCTCCGGGGTTGCGTCCGGGACTGGAGCTG GTCTAACCCACCGTTCCCCCCAGGGACCTGAGTCGGCTCCGGGGTTGCGTCCGGGACTGGAGCTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:103298880..103299071 26863196 MeRIP-seq:(Medium) rs1250565100 Functional Loss SNV dbSNP153 33..33 33 - - - 109465 RMVar_ID_109465 Human_SNP_ID_375833934 m1A Human chr8 + 103300112 103300112 103300112 ATGTGGTAAAATCAGGAATTTGAAGAAAATGGAAATGTTTACATTTTTGTTGACGTGTATTTTTC ATGTGGTAAAATCAGGAATTTGAAGAAAATGGGAATGTTTACATTTTTGTTGACGTGTATTTTTC A G FZD6 Ensembl:ENSG00000164930 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1210913676 Functional Loss SNV dbSNP153 33..33 33 - - - 109466 RMVar_ID_109466 Human_SNP_ID_375837511 m1A Human chr8 - 103317514 103317514 103317514 GTATATTCCAAATCTGACCATTTCTCACTATTACCACCCAGTCTAAGCCACTATTATCTTTCACC GTATATTCCAAATCTGACCATTTCTCACTATTGCCACCCAGTCTAAGCCACTATTATCTTTCACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103317463..103317601 26863196 MeRIP-seq:(Medium) rs921926171 Functional Loss SNV dbSNP153 33..33 33 - - - 109467 RMVar_ID_109467 Human_SNP_ID_375837909 m1A Human chr8 - 103319139 103319139 103319139 ACCCTTACCCTTCGTACTTTAGCTCAACAGTCATTTCCTTCCCCTTTCCCCAGTTTAGGTCAAAG ACCCTTACCCTTCGTACTTTAGCTCAACAGTCGTTTCCTTCCCCTTTCCCCAGTTTAGGTCAAAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103319089..103319335 26863196 MeRIP-seq:(Medium) rs1416723105 Functional Loss SNV dbSNP153 33..33 33 - - - 109468 RMVar_ID_109468 Human_SNP_ID_375838057 m1A Human chr8 + 103319901 103319901 103319901 AACAGAGTTCTTAGGGAAGCTGGCTATAAAAGAGGAAAGTTTATGAGTTTAATGGGAAAGAACTA AACAGAGTTCTTAGGGAAGCTGGCTATAAAAGGGGAAAGTTTATGAGTTTAATGGGAAAGAACTA A G FZD6 Ensembl:ENSG00000164930 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103319851..103320011 26863196 MeRIP-seq:(Medium) rs1405407207 Functional Loss SNV dbSNP153 33..33 33 - - - 109469 RMVar_ID_109469 Human_SNP_ID_375841046 m1A Human chr8 + 103332610 103332610 103332610 CAACGTTTTTATACAACATACTTTAAAATATTAAGGAGTTTTCTTAATTTTGTTTCCTATTAAGT CAACGTTTTTATACAACATACTTTAAAATATTGAGGAGTTTTCTTAATTTTGTTTCCTATTAAGT A G FZD6 Ensembl:ENSG00000164930 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_692640,Human_RBP_ID_1053926,Human_RBP_ID_7794950,Human_RBP_ID_16309093,Human_RBP_ID_17544130,Human_RBP_ID_18125589,Human_RBP_ID_24518312,Human_RBP_ID_27772741 GWAS_ID_15296 109470 RMVar_ID_109470 Human_SNP_ID_375856764 m1A Human chr8 + 103398144 103398144 103398144 CCACTTCTCCAACCTCCTCTCTCTCCTCACCCATCCCCTCTAGCCAACTTAATTCCTCCCTCAGG CCACTTCTCCAACCTCCTCTCTCTCCTCACCCGTCCCCTCTAGCCAACTTAATTCCTCCCTCAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103398093..103398283 26863196 MeRIP-seq:(Medium) rs1202820175 Functional Loss SNV dbSNP153 33..33 33 - - - 109471 RMVar_ID_109471 Human_SNP_ID_375859211 m1A Human chr8 - 103407728 103407728 103407728 CGAAATATAATGGAATTTTACATTGCTTGACTACCATTTGGAAACTTGATGGACTACGGGGACTT CGAAATATAATGGAATTTTACATTGCTTGACTGCCATTTGGAAACTTGATGGACTACGGGGACTT T C AC012213.5,SLC25A32 Ensembl:ENSG00000285982,Ensembl:ENSG00000164933 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:103407642..103407831 26863196 MeRIP-seq:(Medium) rs564720045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88888,Human_RBP_ID_1691977,Human_RBP_ID_2051083,Human_RBP_ID_3129498,Human_RBP_ID_9405674 Human_Splice_Rec_999450,Human_Splice_Rec_999451,Human_Splice_Rec_999458,Human_Splice_Rec_999459,Human_Splice_Rec_999468,Human_Splice_Rec_999469,Human_Splice_Rec_999480,Human_Splice_Rec_999481,Human_Splice_Rec_999496,Human_Splice_Rec_999497 Human_miRNA_ID_2246964,Human_miRNA_ID_2851272 RMVar_hsa_circ_253757,RMVar_hsa_circ_58724,RMVar_hsa_circ_253761,RMVar_hsa_circ_84751,RMVar_hsa_circ_253764,RMVar_hsa_circ_253763,RMVar_hsa_circ_253766,RMVar_hsa_circ_253768,RMVar_hsa_circ_275201,RMVar_hsa_circ_253770,RMVar_hsa_circ_270447,RMVar_hsa_circ_60035 109472 RMVar_ID_109472 Human_SNP_ID_375861144 m1A Human chr8 - 103415066 103415065 103415067 GTCTCCGGCTTCGCTCACGCGCCTTGGGCATAAGAGTCCTCTCGTTGGTCCCGGAGGTGGGGTTG GTCTCCGGCTTCGCTCACGCGCCTTGGGCAT__GAGTCCTCTCGTTGGTCCCGGAGGTGGGGTTG CTT C AC012213.5,SLC25A32 Ensembl:ENSG00000285982,Ensembl:ENSG00000164933 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:103415016..103415087 26863196 MeRIP-seq:(Medium) rs908674888 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4997144,Human_RBP_ID_5514084,Human_RBP_ID_8676971,Human_RBP_ID_9338698 RMVar_hsa_circ_253761,RMVar_hsa_circ_84751 109473 RMVar_ID_109473 Human_SNP_ID_375861145 m1A Human chr8 - 103415066 103415066 103415066 GTCTCCGGCTTCGCTCACGCGCCTTGGGCATAAGAGTCCTCTCGTTGGTCCCGGAGGTGGGGTTG GTCTCCGGCTTCGCTCACGCGCCTTGGGCATAGGAGTCCTCTCGTTGGTCCCGGAGGTGGGGTTG T C AC012213.5,SLC25A32 Ensembl:ENSG00000285982,Ensembl:ENSG00000164933 Protein coding,Protein coding intron,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:103415016..103415087 26863196 MeRIP-seq:(Medium) rs374257876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4997144,Human_RBP_ID_5514084,Human_RBP_ID_8676971,Human_RBP_ID_9338698 RMVar_hsa_circ_253761,RMVar_hsa_circ_84751 109474 RMVar_ID_109474 Human_SNP_ID_375861464 m1A Human chr8 + 103415472 103415472 103415472 AACCGAGATGAAGGTGAAGATGCTGAGCCGGAATCCGGACAATTATGTCCGCGAAACCAAGTTGG AACCGAGATGAAGGTGAAGATGCTGAGCCGGAGTCCGGACAATTATGTCCGCGAAACCAAGTTGG A G DCAF13 Ensembl:ENSG00000164934 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:103415426..103415528 26863196 MeRIP-seq:(Medium) rs1463046788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3973303,Human_RBP_ID_4995669,Human_RBP_ID_8923586,Human_RBP_ID_9313581,Human_RBP_ID_9405675,Human_RBP_ID_18426736,Human_RBP_ID_24239326,Human_RBP_ID_27831499 Human_Splice_Rec_999507,Human_Splice_Rec_999525,Human_Splice_Rec_999543,Human_Splice_Rec_999545,Human_Splice_Rec_999549,Human_Splice_Rec_999553,Human_Splice_Rec_999565,Human_Splice_Rec_999583,Human_Splice_Rec_999589 RMVar_hsa_circ_95531,RMVar_hsa_circ_253771 109475 RMVar_ID_109475 Human_SNP_ID_375861465 m1A Human chr8 - 103415473 103415473 103415473 TCCAACTTGGTTTCGCGGACATAATTGTCCGGATTCCGGCTCAGCATCTTCACCTTCATCTCGGT TCCAACTTGGTTTCGCGGACATAATTGTCCGGTTTCCGGCTCAGCATCTTCACCTTCATCTCGGT T A AC012213.5 Ensembl:ENSG00000285982 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103415426..103415525 26863196 MeRIP-seq:(Medium) rs770268158 Functional Loss SNV dbSNP153 33..33 33 - - - 109476 RMVar_ID_109476 Human_SNP_ID_375861470 m1A Human chr8 - 103415485 103415485 103415485 CCTCTCTGTAAGTCCAACTTGGTTTCGCGGACATAATTGTCCGGATTCCGGCTCAGCATCTTCAC CCTCTCTGTAAGTCCAACTTGGTTTCGCGGACGTAATTGTCCGGATTCCGGCTCAGCATCTTCAC T C AC012213.5 Ensembl:ENSG00000285982 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:103415435..103415527 26863196 MeRIP-seq:(Medium) rs1203452758 Functional Loss SNV dbSNP153 33..33 33 - - - 109477 RMVar_ID_109477 Human_SNP_ID_375896735 m1A Human chr8 - 103559193 103559190 103559193 GGAAGTGGGGAGGAAGAGGAAGAGAAATAAGAAGATAATGGTGAGGAACAGGATGGAGATGAAGA GGAAGTGGGGAGGAAGAGGAAGAGAAATAAGA___TAATGGTGAGGAACAGGATGGAGATGAAGA ATCT A PTMAP15 Ensembl:ENSG00000255105 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:103559145..103559210 26863196 MeRIP-seq:(Medium) rs1382564469 Functional Loss DEL dbSNP153 33..35 33 - - - 109478 RMVar_ID_109478 Human_SNP_ID_69824621 m1A Human chr2 - 45009104 45009104 45009104 GGGCGGGCGGGGACGCAGCCGGCACCATGTCCATGCTGCCCACCTTCGGCTTCACGCAGGAGCAA GGGCGGGCGGGGACGCAGCCGGCACCATGTCCGTGCTGCCCACCTTCGGCTTCACGCAGGAGCAA T C SIX2 Ensembl:ENSG00000170577 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:45009018..45009193 26863196 MeRIP-seq:(Medium) rs760590442 Functional Loss SNV dbSNP153 33..33 33 - - - 109479 RMVar_ID_109479 Human_SNP_ID_69824737 m1A Human chr2 - 45009378 45009378 45009378 GAAGCGAGCGAGGGAACGGCGGGCGGGCGCGGAGCATGCGGAGCGGCGCCCCGGGCGGCCCCCGG GAAGCGAGCGAGGGAACGGCGGGCGGGCGCGGGGCATGCGGAGCGGCGCCCCGGGCGGCCCCCGG T C SIX2 Ensembl:ENSG00000170577 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr2:45009088..45009450;chr2:45009075..45009450;chr2:45009101..45009450;chr2:45009086..45009450;chr2:45009273..45009425 26863196 MeRIP-seq:(Medium) rs1487016006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4610230 109480 RMVar_ID_109480 Human_SNP_ID_69876275 m1A Human chr2 + 45188136 45188136 45188136 AGGGCCCATCACCCAAAAAAAACTTTCCATGCAGTCATCATGGTGAAACTTCTTTAAAGCCAGGT AGGGCCCATCACCCAAAAAAAACTTTCCATGCGGTCATCATGGTGAAACTTCTTTAAAGCCAGGT A G AC009236.2 Ensembl:ENSG00000286728 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:45188109..45188196 26863410 MeRIP-seq:(Medium) rs761183207 Functional Loss SNV dbSNP153 33..33 33 - - - 109481 RMVar_ID_109481 Human_SNP_ID_69995160 m1A Human chr2 - 45605415 45605415 45605415 TTCTAGATGTCATCATTGCCAAGAAGAGCGAAAGTACAGGTCCAGGATGTGGTACTGAAAGATGA TTCTAGATGTCATCATTGCCAAGAAGAGCGAAGGTACAGGTCCAGGATGTGGTACTGAAAGATGA T C SRBD1 Ensembl:ENSG00000068784 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:45605352..45605421 26863196 MeRIP-seq:(Medium) rs749259845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19001591,Human_RBP_ID_27817053 Human_Splice_Rec_241730,Human_Splice_Rec_241731,Human_Splice_Rec_241802,Human_Splice_Rec_241803 RMVar_hsa_circ_367808,RMVar_hsa_circ_199514,RMVar_hsa_circ_65195,RMVar_hsa_circ_59101,RMVar_hsa_circ_295756 109482 RMVar_ID_109482 Human_SNP_ID_70020453 m1A Human chr2 + 45693106 45693106 45693106 GTGGGATGAGAAGTCAGGAACAGATCCTGAGGAGTGCGGGGTAGGGGAGTGAAGTAGGTGGGAGG GTGGGATGAGAAGTCAGGAACAGATCCTGAGGGGTGCGGGGTAGGGGAGTGAAGTAGGTGGGAGG A G PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:45693039..45693177 26863196 MeRIP-seq:(Medium) rs116305061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28332,RMVar_hsa_circ_120598,RMVar_hsa_circ_98469,RMVar_hsa_circ_199531,RMVar_hsa_circ_318510,RMVar_hsa_circ_199532,RMVar_hsa_circ_199533 109483 RMVar_ID_109483 Human_SNP_ID_70020845 m1A Human chr2 + 45694662 45694662 45694662 TGGTTAGAGTGGCTGAGAAAGGTTCAGGGAGGACATGAGTGAGACTTCGAATGGTGGGTGGATTG TGGTTAGAGTGGCTGAGAAAGGTTCAGGGAGGGCATGAGTGAGACTTCGAATGGTGGGTGGATTG A G PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:45694612..45694809 26863196 MeRIP-seq:(Medium) rs1558564858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13902538,Human_RBP_ID_22993189 RMVar_hsa_circ_28332,RMVar_hsa_circ_120598,RMVar_hsa_circ_98469,RMVar_hsa_circ_199531,RMVar_hsa_circ_318510,RMVar_hsa_circ_199532,RMVar_hsa_circ_199533 109484 RMVar_ID_109484 Human_SNP_ID_70026848 m1A Human chr2 + 45716612 45716606 45716612 GAAGAAAGGAAGGAAGGAAGGAGAGGGAGAAGAAGAAGAAGAAGGAGAAGGAGAAGAAGAAGAAG GAAGAAAGGAAGGAAGGAAGGAGAGGG______AGAAGAAGAAGGAGAAGGAGAAGAAGAAGAAG GAGAAGA G PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:45716566..45716699 26863196 MeRIP-seq:(Medium) rs879888426 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_24546039 RMVar_hsa_circ_24726,RMVar_hsa_circ_28332,RMVar_hsa_circ_99961,RMVar_hsa_circ_24961,RMVar_hsa_circ_199538 109485 RMVar_ID_109485 Human_SNP_ID_70026849 m1A Human chr2 + 45716612 45716606 45716612 GAAGAAAGGAAGGAAGGAAGGAGAGGGAGAAGAAGAAGAAGAAGGAGAAGGAGAAGAAGAAGAAG GAAGAAAGGAAGGAAGGAAGGAGAGGGAGA___AGAAGAAGAAGGAGAAGGAGAAGAAGAAGAAG GAGAAGA GAGA PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:45716566..45716699 26863196 MeRIP-seq:(Medium) rs879888426 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_24546039 RMVar_hsa_circ_24726,RMVar_hsa_circ_28332,RMVar_hsa_circ_99961,RMVar_hsa_circ_24961,RMVar_hsa_circ_199538 109486 RMVar_ID_109486 Human_SNP_ID_70027011 m1A Human chr2 - 45716786 45716786 45716786 AGGTCTCCCCAGCCATGCTGAACTGTGAGTCAATTAAACCTCTATTCTTTATAAATTCTGCAGTC AGGTCTCCCCAGCCATGCTGAACTGTGAGTCAGTTAAACCTCTATTCTTTATAAATTCTGCAGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:45716571..45716846 26863196 MeRIP-seq:(Medium) rs543582538 Functional Loss SNV dbSNP153 33..33 33 - - - 109487 RMVar_ID_109487 Human_SNP_ID_70050614 m1A Human chr2 - 45801610 45801610 45801610 TCCCCATCTTCCTTCCCAGCACCTCATCCTAAATTCCCAGCATCTTGAAGCCTGACTGTGCAGAG TCCCCATCTTCCTTCCCAGCACCTCATCCTAATTTCCCAGCATCTTGAAGCCTGACTGTGCAGAG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:45801559..45801680 26863196 MeRIP-seq:(Medium) rs957724283 Functional Loss SNV dbSNP153 33..33 33 - - - 109488 RMVar_ID_109488 Human_SNP_ID_70190262 m1A Human chr2 + 46297588 46297588 46297588 AGCCACTTTTTTTTTTCTTTGAAAACTCAGAAAAGTGACTCCTTTTCCAGGGAAAAAGGAACTTG AGCCACTTTTTTTTTTCTTTGAAAACTCAGAAGAGTGACTCCTTTTCCAGGGAAAAAGGAACTTG A G EPAS1 Ensembl:ENSG00000116016 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:46297497..46297597 32194978 MeRIP-seq:(Medium) rs1425866224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_146151 109489 RMVar_ID_109489 Human_SNP_ID_70190409 m1A Human chr2 - 46297920 46297920 46297920 CGGACGCCCGCTTACCTTTTCTTCTCCTTGTCAGCTGTCATTGTCGCTGTGGCCCTTTGAGACGT CGGACGCCCGCTTACCTTTTCTTCTCCTTGTCGGCTGTCATTGTCGCTGTGGCCCTTTGAGACGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46297872..46297962 26863196 MeRIP-seq:(Medium) rs1219410135 Functional Loss SNV dbSNP153 33..33 33 - - - 109490 RMVar_ID_109490 Human_SNP_ID_70195186 m1A Human chr2 + 46315303 46315302 46315303 GAAAGCTGATGGCCGTGAGAGGAGCAGGTTTGAAAATCACTGAATGAAGTCATGTTGTACAGAGG GAAAGCTGATGGCCGTGAGAGGAGCAGGTTTG_AAATCACTGAATGAAGTCATGTTGTACAGAGG GA G EPAS1 Ensembl:ENSG00000116016 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:46315301..46315384 26863196 MeRIP-seq:(Medium) rs1273201968 Functional Loss DEL dbSNP153 33..33 33 - - - 109491 RMVar_ID_109491 Human_SNP_ID_70203180 m1A Human chr2 + 46346826 46346826 46346826 GGCCATGGGGATGTCCTGGCCAGAGGTATGATAGGCTGACAGTAACCTTTCCGGGACTAACCCCT GGCCATGGGGATGTCCTGGCCAGAGGTATGATGGGCTGACAGTAACCTTTCCGGGACTAACCCCT A G EPAS1 Ensembl:ENSG00000116016 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:46346823..46347025 26863196 MeRIP-seq:(Medium) rs1558596411 Functional Loss SNV dbSNP153 33..33 33 - - - 109492 RMVar_ID_109492 Human_SNP_ID_70206994 m1A Human chr2 - 46360742 46360742 46360742 GGCCTGATGTTGCCCTACCTTCCAGGTGGCTGACTTGAGGTTGACAGTACGGCCTCTGTTGGTGA GGCCTGATGTTGCCCTACCTTCCAGGTGGCTGTCTTGAGGTTGACAGTACGGCCTCTGTTGGTGA T A LINC01820 RNACentral:URS0000D59F36 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:46360656..46360934 32194978 MeRIP-seq:(Medium) rs1324579632 Functional Loss SNV dbSNP153 33..33 33 - - - 109493 RMVar_ID_109493 Human_SNP_ID_70207077 m1A Human chr2 + 46360934 46360934 46360934 CCAGGTGAAAGTCTACAACAACTGCCCTCCTCACAATAGTCTGTGTGGCTACAAGGAGCCCCTGC CCAGGTGAAAGTCTACAACAACTGCCCTCCTCCCAATAGTCTGTGTGGCTACAAGGAGCCCCTGC A C EPAS1 Ensembl:ENSG00000116016 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:46360755..46360984 32194978 MeRIP-seq:(Medium) rs759148245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_241952,Human_Splice_Rec_241962,Human_Splice_Rec_241996 RMVar_hsa_circ_276331,RMVar_hsa_circ_103849,RMVar_hsa_circ_285335,RMVar_hsa_circ_370474,RMVar_hsa_circ_199559,RMVar_hsa_circ_371727,RMVar_hsa_circ_199560,RMVar_hsa_circ_199561,RMVar_hsa_circ_199562,RMVar_hsa_circ_291568,RMVar_hsa_circ_371136 109494 RMVar_ID_109494 Human_SNP_ID_70207100 m1A Human chr2 - 46360989 46360989 46360989 ATGTCCATGTGGGATGGGTGCTGGATTGGTTCACACATGATGATGAGGCAGGACAGCAGGGGCTC ATGTCCATGTGGGATGGGTGCTGGATTGGTTCGCACATGATGATGAGGCAGGACAGCAGGGGCTC T C LINC01820 RNACentral:URS0000D59F36 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:46360939..46361010 26863196 MeRIP-seq:(Medium) rs139953529 Functional Loss SNV dbSNP153 33..33 33 - - - 109495 RMVar_ID_109495 Human_SNP_ID_70211310 m1A Human chr2 - 46375648 46375647 46375648 GAGAAACAGAGCTGAGCTTAGGGAGGTGGGGCAGGGGTGTGCACCACAGGCTCAGCAGATCGCAT GAGAAACAGAGCTGAGCTTAGGGAGGTGGGGC_GGGGTGTGCACCACAGGCTCAGCAGATCGCAT CT C LINC01820 RNACentral:URS0000D59F36 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:46375645..46375793 26863196 MeRIP-seq:(Medium) rs753130534 Functional Loss DEL dbSNP153 33..33 33 - - - 109496 RMVar_ID_109496 Human_SNP_ID_70213883 m1A Human chr2 - 46382492 46382486 46382492 TTGCTGTTCTCCCCGGGACTGATGGCAGATGGAGGCTGTGGCAGCGGCAGATGTCTCAGGGGATG TTGCTGTTCTCCCCGGGACTGATGGCAGATGG______TGGCAGCGGCAGATGTCTCAGGGGATG ACAGCCT A LINC01820 RNACentral:URS0000D59F36 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:46382441..46384567 32194978 MeRIP-seq:(Medium) rs907821811 Functional Loss DEL dbSNP153 33..38 33 - - - 109497 RMVar_ID_109497 Human_SNP_ID_70214603 m1A Human chr2 + 46384647 46384647 46384647 CCTGCAAGGAGGGGACCTCCTCAGAGCCCTGGACCAGGCCACCTGAGCCAGGCCTTCTACCTGGG CCTGCAAGGAGGGGACCTCCTCAGAGCCCTGGTCCAGGCCACCTGAGCCAGGCCTTCTACCTGGG A T EPAS1 Ensembl:ENSG00000116016 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:46384630..46384814 26863196 MeRIP-seq:(Medium) rs565332983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143146 Human_miRNA_ID_2082326,Human_miRNA_ID_2268404 RMVar_hsa_circ_106876,RMVar_hsa_circ_199565,RMVar_hsa_circ_97040,RMVar_hsa_circ_199566 109498 RMVar_ID_109498 Human_SNP_ID_70260526 m1A Human chr2 + 46542864 46542852 46542864 GCGGGGATCCGGGCGGCGACCGCGGCGGCGGCAGCGCCCCGGGCCCGCCGCCCCCTCCCCTCCTG GCGGGGATCCGGGCGGCGACC____________GCGCCCCGGGCCCGCCGCCCCCTCCCCTCCTG CGCGGCGGCGGCA C RHOQ Ensembl:ENSG00000119729 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr2:46542771..46542921 26863410 MeRIP-seq:(Medium) rs1474776853 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_264359,Human_RBP_ID_4622377,Human_RBP_ID_5322052 109499 RMVar_ID_109499 Human_SNP_ID_70271196 m1A Human chr2 + 46582753 46582753 46582753 TTTATACTTGAAAATGACAGCCTTAAATGCTCATATCAGTCACAAATCTAGGATGTACTGTCTTG TTTATACTTGAAAATGACAGCCTTAAATGCTCGTATCAGTCACAAATCTAGGATGTACTGTCTTG A G RHOQ Ensembl:ENSG00000119729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1459243164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_456075,Human_miRNA_ID_458036,Human_miRNA_ID_1745113 109500 RMVar_ID_109500 Human_SNP_ID_70271197 m1A Human chr2 + 46582753 46582753 46582753 TTTATACTTGAAAATGACAGCCTTAAATGCTCATATCAGTCACAAATCTAGGATGTACTGTCTTG TTTATACTTGAAAATGACAGCCTTAAATGCTCTTATCAGTCACAAATCTAGGATGTACTGTCTTG A T RHOQ Ensembl:ENSG00000119729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1459243164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_456075,Human_miRNA_ID_458036,Human_miRNA_ID_1745113 109501 RMVar_ID_109501 Human_SNP_ID_70278736 m1A Human chr2 - 46612338 46612338 46612338 AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCATTGGAAACATTTTTATTTGCAGTTATTTTGTC AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCGTTGGAAACATTTTTATTTGCAGTTATTTTGTC T C PIGF Ensembl:ENSG00000151665 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1824050 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22595243 Human_Splice_Rec_242140,Human_Splice_Rec_242158,Human_Splice_Rec_242168,Human_Splice_Rec_242174 RMVar_hsa_circ_199572,RMVar_hsa_circ_301100,RMVar_hsa_circ_369497,RMVar_hsa_circ_199573,RMVar_hsa_circ_199574,RMVar_hsa_circ_281678 109502 RMVar_ID_109502 Human_SNP_ID_70278737 m1A Human chr2 - 46612338 46612338 46612338 AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCATTGGAAACATTTTTATTTGCAGTTATTTTGTC AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCCTTGGAAACATTTTTATTTGCAGTTATTTTGTC T G PIGF Ensembl:ENSG00000151665 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1824050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22595243 Human_Splice_Rec_242140,Human_Splice_Rec_242158,Human_Splice_Rec_242168,Human_Splice_Rec_242174 RMVar_hsa_circ_199572,RMVar_hsa_circ_301100,RMVar_hsa_circ_369497,RMVar_hsa_circ_199573,RMVar_hsa_circ_199574,RMVar_hsa_circ_281678 109503 RMVar_ID_109503 Human_SNP_ID_70280457 m1A Human chr2 + 46617293 46617293 46617293 AGGGGAACCGTCGTGGGGAAGGATGGTGTGCGAAAAATGTGAGTTAAGGGGCCGCTTCTGCGGGA AGGGGAACCGTCGTGGGGAAGGATGGTGTGCGTAAAATGTGAGTTAAGGGGCCGCTTCTGCGGGA A T CRIPT Ensembl:ENSG00000119878 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:46617208..46618805;chr2:46617199..46617357 26863196 MeRIP-seq:(Medium) rs1179009721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_551733,Human_RBP_ID_923197,Human_RBP_ID_4623278,Human_RBP_ID_9330441,Human_RBP_ID_18421760,Human_RBP_ID_19001600,Human_RBP_ID_22452166,Human_RBP_ID_23211529,Human_RBP_ID_23874320,Human_RBP_ID_27817054 Human_Splice_Rec_242185 RMVar_hsa_circ_102068,RMVar_hsa_circ_199575 109504 RMVar_ID_109504 Human_SNP_ID_70303690 m1A Human chr2 - 46699248 46699248 46699248 CCAGCTCCGCCGGATGCCCCCGCCAGGCCCCCACCCCCTTCCCTGCCGCCTCCCCTTCTTCACCC CCAGCTCCGCCGGATGCCCCCGCCAGGCCCCCCCCCCCTTCCCTGCCGCCTCCCCTTCTTCACCC T G lnc-PIGF-4,lnc-PIGF-4:2,lnc-PIGF-4:3 RNACentral:URS0000D5D9A2,RNACentral:URS0000D5E189,RNACentral:URS0000D57C4C lincRNA,lincRNA,lincRNA exon,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:46699201..46699375 26863196 MeRIP-seq:(Medium) rs1043523721 Functional Loss SNV dbSNP153 33..33 33 - - - 109505 RMVar_ID_109505 Human_SNP_ID_70303783 m1A Human chr2 - 46699506 46699506 46699506 GGCACTGGGGCACCGAGAGGCGGCCGCGGACGACGGCGCGGGGGCCGGGGAGCAGGCGGCGGGCC GGCACTGGGGCACCGAGAGGCGGCCGCGGACGGCGGCGCGGGGGCCGGGGAGCAGGCGGCGGGCC T C lnc-PIGF-4,lnc-PIGF-4:2,lnc-PIGF-4:3 RNACentral:URS0000D5D9A2,RNACentral:URS0000D5E189,RNACentral:URS0000D57C4C lincRNA,lincRNA,lincRNA exon,exon,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:46699497..46699623 26863196 MeRIP-seq:(Medium) rs1007630785 Functional Loss SNV dbSNP153 33..33 33 - - - 109506 RMVar_ID_109506 Human_SNP_ID_70320824 m1A Human chr2 + 46762123 46762123 46762123 CTTTTAAAGCAAAATGGGGATTGAAGGGACTTATAATTTCTGTTGTTTCTAATTAAAGTCCCTGA CTTTTAAAGCAAAATGGGGATTGAAGGGACTTTTAATTTCTGTTGTTTCTAATTAAAGTCCCTGA A T SOCS5,LINC01118 Ensembl:ENSG00000171150,Ensembl:ENSG00000222005 Protein coding,lincRNA 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17771942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2648970,Human_RBP_ID_18317446 GWAS_ID_15297,GWAS_ID_15298,GWAS_ID_15299,GWAS_ID_15300,GWAS_ID_15301,GWAS_ID_15302,GWAS_ID_15303,GWAS_ID_15304,GWAS_ID_15305,GWAS_ID_15306,GWAS_ID_15307,GWAS_ID_15308,GWAS_ID_15309,GWAS_ID_15310,GWAS_ID_15311,GWAS_ID_15312,GWAS_ID_15313,GWAS_ID_15314,GWAS_ID_15315 109507 RMVar_ID_109507 Human_SNP_ID_70365201 m1A Human chr2 + 46915842 46915842 46915842 CGCCCCCCCCCCCCCCCCGACCTGCCCTGCGCACGCGCGCTCCCTGCCGCCCGCCCATTGGCGCC CGCCCCCCCCCCCCCCCCGACCTGCCCTGCGCCCGCGCGCTCCCTGCCGCCCGCCCATTGGCGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46915840..46915971 26863196 MeRIP-seq:(Medium) rs1406173600 Functional Loss SNV dbSNP153 33..33 33 - - - 109508 RMVar_ID_109508 Human_SNP_ID_70365212 m1A Human chr2 - 46915854 46915853 46915855 GAGGGGCCCGGCGGCGCCAATGGGCGGGCGGCAGGGAGCGCGCGTGCGCAGGGCAGGTCGGGGGG GAGGGGCCCGGCGGCGCCAATGGGCGGGCGG__GGGAGCGCGCGTGCGCAGGGCAGGTCGGGGGG CTG C MCFD2 Ensembl:ENSG00000180398 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:46915850..46916006 26863196 MeRIP-seq:(Medium) rs1443818777 Functional Loss DEL dbSNP153 32..33 33 - - - 109509 RMVar_ID_109509 Human_SNP_ID_70365213 m1A Human chr2 - 46915854 46915854 46915854 GAGGGGCCCGGCGGCGCCAATGGGCGGGCGGCAGGGAGCGCGCGTGCGCAGGGCAGGTCGGGGGG GAGGGGCCCGGCGGCGCCAATGGGCGGGCGGCGGGGAGCGCGCGTGCGCAGGGCAGGTCGGGGGG T C MCFD2 Ensembl:ENSG00000180398 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:46915850..46916006 26863196 MeRIP-seq:(Medium) rs1277280535 Functional Loss SNV dbSNP153 33..33 33 - - - 109510 RMVar_ID_109510 Human_SNP_ID_70372399 m1A Human chr2 + 46941522 46941522 46941522 GGCCGGGTCTCCACTTCTTGGCCGCACCTTCCATGACAGCGCCCGCGAGAAGATGGCTGCGAAGG GGCCGGGTCTCCACTTCTTGGCCGCACCTTCCGTGACAGCGCCCGCGAGAAGATGGCTGCGAAGG A G TTC7A Ensembl:ENSG00000068724 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:46941261..46941662 26863196 MeRIP-seq:(Medium) rs528870284 Functional Loss SNV dbSNP153 33..33 33 - - - 109511 RMVar_ID_109511 Human_SNP_ID_70379107 m1A Human chr2 - 46964253 46964253 46964253 CCGGGGCTTCCCTTTGGCCTTCCCTTGCTGGAAGGCACCTCTTCCCCTCAACTGTAGGTGATTCA CCGGGGCTTCCCTTTGGCCTTCCCTTGCTGGAGGGCACCTCTTCCCCTCAACTGTAGGTGATTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46964248..46964433 26863196 MeRIP-seq:(Medium) rs1373076211 Functional Loss SNV dbSNP153 33..33 33 - - - 109512 RMVar_ID_109512 Human_SNP_ID_70385720 m1A Human chr2 - 46986492 46986492 46986492 CCTCTTTCCCCCCCAGCACAGAGCACTGCCTGACCGTCTCCACCACAGGCTCCCCTCTGGGACGG CCTCTTTCCCCCCCAGCACAGAGCACTGCCTGTCCGTCTCCACCACAGGCTCCCCTCTGGGACGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:46986489..46986607 26863196 MeRIP-seq:(Medium) rs1416281864 Functional Loss SNV dbSNP153 33..33 33 - - - 109513 RMVar_ID_109513 Human_SNP_ID_70388009 m1A Human chr2 + 46994141 46994141 46994141 TCTAGGAGAGGAGAGAAGAGAAAAGATGAGGTAGGAGCCGTCTGAGGCCAGCAGAGGGGTGGGAG TCTAGGAGAGGAGAGAAGAGAAAAGATGAGGTGGGAGCCGTCTGAGGCCAGCAGAGGGGTGGGAG A G TTC7A Ensembl:ENSG00000068724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46994128..46994331 26863196 MeRIP-seq:(Medium) rs1244025818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308701,RMVar_hsa_circ_35049,RMVar_hsa_circ_71095,RMVar_hsa_circ_34054,RMVar_hsa_circ_60739,RMVar_hsa_circ_267327,RMVar_hsa_circ_276720,RMVar_hsa_circ_315871,RMVar_hsa_circ_344536,RMVar_hsa_circ_66935,RMVar_hsa_circ_35421,RMVar_hsa_circ_199585,RMVar_hsa_circ_48114,RMVar_hsa_circ_199584,RMVar_hsa_circ_199586,RMVar_hsa_circ_341616 109514 RMVar_ID_109514 Human_SNP_ID_70388727 m1A Human chr2 + 46996262 46996262 46996262 AGCATCAGAAGCCAAGCACACAGGAGTCATCTACATGGTCAGGTCCAAGTCCTCCGACCAAGGGG AGCATCAGAAGCCAAGCACACAGGAGTCATCTCCATGGTCAGGTCCAAGTCCTCCGACCAAGGGG A C TTC7A Ensembl:ENSG00000068724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46996119..46996369 26863196 MeRIP-seq:(Medium) rs913013128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308701,RMVar_hsa_circ_71095,RMVar_hsa_circ_34054,RMVar_hsa_circ_7334,RMVar_hsa_circ_267327,RMVar_hsa_circ_315871,RMVar_hsa_circ_344536,RMVar_hsa_circ_66935,RMVar_hsa_circ_35421,RMVar_hsa_circ_199585,RMVar_hsa_circ_48114,RMVar_hsa_circ_199584,RMVar_hsa_circ_45574,RMVar_hsa_circ_199587 109515 RMVar_ID_109515 Human_SNP_ID_70391666 m1A Human chr2 - 47006046 47006046 47006046 GCTGCATGGCCGGCCGTACCTCCGAGAGCATGACGTACTGTCCCCTTCTGCCCAACGTGATGCTC GCTGCATGGCCGGCCGTACCTCCGAGAGCATGTCGTACTGTCCCCTTCTGCCCAACGTGATGCTC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:47005983..47006068 26863410 MeRIP-seq:(Medium) rs374669143 Functional Loss SNV dbSNP153 33..33 33 - - - 109516 RMVar_ID_109516 Human_SNP_ID_70393350 m1A Human chr2 - 47011424 47011424 47011424 CTGCCCTCACAGCTCACTCACCCAGCGAAGGGACCCGATGCAGACCTTCGCGGCCATCAGGGGCA CTGCCCTCACAGCTCACTCACCCAGCGAAGGGGCCCGATGCAGACCTTCGCGGCCATCAGGGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47006703..47021886 32194978 MeRIP-seq:(Medium) rs1416197392 Functional Loss SNV dbSNP153 33..33 33 - - - 109517 RMVar_ID_109517 Human_SNP_ID_70407303 m1A Human chr2 + 47056715 47056713 47056715 CATTTGTAGCCTGCCGAGAGAAAGCACAGAGGAGAGGGGGTGGAGAGAGATGGAGGGAAGAGGAG CATTTGTAGCCTGCCGAGAGAAAGCACAGAG__GAGGGGGTGGAGAGAGATGGAGGGAAGAGGAG GGA G TTC7A Ensembl:ENSG00000068724 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:47056701..47056853 26863196 MeRIP-seq:(Medium) rs1262976756 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_34054,RMVar_hsa_circ_7334,RMVar_hsa_circ_267525,RMVar_hsa_circ_315024,RMVar_hsa_circ_23902 109518 RMVar_ID_109518 Human_SNP_ID_70408608 m1A Human chr2 + 47060799 47060799 47060799 AGCTGAGCTGTTCATGGAGCAGCAGCACCTCAAGGAAGCAGGTTTCTGCATCCAGGAGGCGGCGG AGCTGAGCTGTTCATGGAGCAGCAGCACCTCAGGGAAGCAGGTTTCTGCATCCAGGAGGCGGCGG A G TTC7A Ensembl:ENSG00000068724 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47051819..47060858 32194978 MeRIP-seq:(Medium) rs143687375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_242372,Human_Splice_Rec_242410,Human_Splice_Rec_242482,Human_Splice_Rec_242518,Human_Splice_Rec_242558,Human_Splice_Rec_242598,Human_Splice_Rec_242620,Human_Splice_Rec_242650,Human_Splice_Rec_242664,Human_Splice_Rec_242682,Human_Splice_Rec_242702,Human_Splice_Rec_242712 RMVar_hsa_circ_34054,RMVar_hsa_circ_7334,RMVar_hsa_circ_267525,RMVar_hsa_circ_315024,RMVar_hsa_circ_23902,RMVar_hsa_circ_199594,RMVar_hsa_circ_93243 109519 RMVar_ID_109519 Human_SNP_ID_70442014 m1A Human chr2 - 47165582 47165582 47165582 GACAGGAGTAAGAGCCTTTGGCAGTATATGGTAGGAGGAAAATCAAAGTACTGTTACGAAGGCCA GACAGGAGTAAGAGCCTTTGGCAGTATATGGTGGGAGGAAAATCAAAGTACTGTTACGAAGGCCA T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47165580..47165696 26863196 MeRIP-seq:(Medium) rs1480091547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13905634,Human_RBP_ID_23874717 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 109520 RMVar_ID_109520 Human_SNP_ID_70442015 m1A Human chr2 - 47165582 47165582 47165582 GACAGGAGTAAGAGCCTTTGGCAGTATATGGTAGGAGGAAAATCAAAGTACTGTTACGAAGGCCA GACAGGAGTAAGAGCCTTTGGCAGTATATGGTCGGAGGAAAATCAAAGTACTGTTACGAAGGCCA T G CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47165580..47165696 26863196 MeRIP-seq:(Medium) rs1480091547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13905634,Human_RBP_ID_23874717 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 109521 RMVar_ID_109521 Human_SNP_ID_70443719 m1A Human chr2 - 47170735 47170735 47170735 TAGGCTGACCAACTGACTGAAGAGCAGATTGCAGGTGAGAAATACTCAGCTAGATTGTACCCATT TAGGCTGACCAACTGACTGAAGAGCAGATTGCGGGTGAGAAATACTCAGCTAGATTGTACCCATT T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:47170726..47170800 26863410 MeRIP-seq:(Medium) rs1324754202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243738,Human_RBP_ID_777130,Human_RBP_ID_1587373,Human_RBP_ID_4610544,Human_RBP_ID_6927068,Human_RBP_ID_9383599,Human_RBP_ID_13905806,Human_RBP_ID_19097375,Human_RBP_ID_22452173,Human_RBP_ID_22478042,Human_RBP_ID_22595250,Human_RBP_ID_22742948,Human_RBP_ID_23874728,Human_RBP_ID_26339260 Human_Splice_Rec_242756,Human_Splice_Rec_242757,Human_Splice_Rec_242772,Human_Splice_Rec_242773,Human_Splice_Rec_242782,Human_Splice_Rec_242783,Human_Splice_Rec_242788,Human_Splice_Rec_242789,Human_Splice_Rec_242797,Human_Splice_Rec_242806,Human_Splice_Rec_242807,Human_Splice_Rec_242816,Human_Splice_Rec_242817,Human_Splice_Rec_242826,Human_Splice_Rec_242827,Human_Splice_Rec_242836,Human_Splice_Rec_242837,Human_Splice_Rec_242854,Human_Splice_Rec_242855,Human_Splice_Rec_242864,Human_Splice_Rec_242865,Human_Splice_Rec_242874,Human_Splice_Rec_242875,Human_Splice_Rec_242890,Human_Splice_Rec_242891,Human_Splice_Rec_242904,Human_Splice_Rec_242905,Human_Splice_Rec_242914,Human_Splice_Rec_242915 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 109522 RMVar_ID_109522 Human_SNP_ID_70443722 m1A Human chr2 - 47170766 47170766 47170766 AAGTCACTAACCTTCCTCTTTGATCTCTTTGTAGGCTGACCAACTGACTGAAGAGCAGATTGCAG AAGTCACTAACCTTCCTCTTTGATCTCTTTGTTGGCTGACCAACTGACTGAAGAGCAGATTGCAG T A CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:47170726..47170775 26863196 MeRIP-seq:(Medium) rs113621416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61362,Human_RBP_ID_777130,Human_RBP_ID_2649327,Human_RBP_ID_4633083,Human_RBP_ID_13905806,Human_RBP_ID_19097375,Human_RBP_ID_20579641,Human_RBP_ID_22452173,Human_RBP_ID_22670057,Human_RBP_ID_22742948,Human_RBP_ID_23891657,Human_RBP_ID_25546948 Human_Splice_Rec_242757,Human_Splice_Rec_242773,Human_Splice_Rec_242783,Human_Splice_Rec_242789,Human_Splice_Rec_242797,Human_Splice_Rec_242807,Human_Splice_Rec_242817,Human_Splice_Rec_242827,Human_Splice_Rec_242837,Human_Splice_Rec_242855,Human_Splice_Rec_242865,Human_Splice_Rec_242875,Human_Splice_Rec_242891,Human_Splice_Rec_242905,Human_Splice_Rec_242915 RMVar_hsa_circ_58967 109523 RMVar_ID_109523 Human_SNP_ID_70445711 m1A Human chr2 + 47175985 47175985 47175985 GGCCCCGCGCGCTCCTCCCGCCCCCTGGGCGCATGGCGGCCGCAAGCGGACAAAGGCGCTTCCTG GGCCCCGCGCGCTCCTCCCGCCCCCTGGGCGCCTGGCGGCCGCAAGCGGACAAAGGCGCTTCCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47175980..47176221 26863196 MeRIP-seq:(Medium) rs1311503693 Functional Loss SNV dbSNP153 33..33 33 - - - 109524 RMVar_ID_109524 Human_SNP_ID_70445712 m1A Human chr2 + 47175985 47175985 47175985 GGCCCCGCGCGCTCCTCCCGCCCCCTGGGCGCATGGCGGCCGCAAGCGGACAAAGGCGCTTCCTG GGCCCCGCGCGCTCCTCCCGCCCCCTGGGCGCGTGGCGGCCGCAAGCGGACAAAGGCGCTTCCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47175980..47176221 26863196 MeRIP-seq:(Medium) rs1311503693 Functional Loss SNV dbSNP153 33..33 33 - - - 109525 RMVar_ID_109525 Human_SNP_ID_70445979 m1A Human chr2 - 47176461 47176461 47176461 GAGCTGAGTGGTTGTGTGGTCGCGTCTCGGAAACCGGTAGCGCTTGCAGCATGGTGAGTGCATCG GAGCTGAGTGGTTGTGTGGTCGCGTCTCGGAAGCCGGTAGCGCTTGCAGCATGGTGAGTGCATCG T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:47170726..47176537;chr2:47170726..47176550 26863196 MeRIP-seq:(Medium) rs996505212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243744,Human_RBP_ID_280946,Human_RBP_ID_551915,Human_RBP_ID_777139,Human_RBP_ID_1587405,Human_RBP_ID_1918956,Human_RBP_ID_3627829,Human_RBP_ID_4610554,Human_RBP_ID_5322063,Human_RBP_ID_5502280,Human_RBP_ID_6927160,Human_RBP_ID_8520497,Human_RBP_ID_9107303,Human_RBP_ID_9330450,Human_RBP_ID_9383602,Human_RBP_ID_17963932,Human_RBP_ID_18761777,Human_RBP_ID_19097376,Human_RBP_ID_22449787,Human_RBP_ID_23133040,Human_RBP_ID_23874803,Human_RBP_ID_26339263 Human_Splice_Rec_242755,Human_Splice_Rec_242771,Human_Splice_Rec_242781,Human_Splice_Rec_242787,Human_Splice_Rec_242805,Human_Splice_Rec_242825,Human_Splice_Rec_242833,Human_Splice_Rec_242889 109526 RMVar_ID_109526 Human_SNP_ID_70446018 m1A Human chr2 + 47176489 47176489 47176489 CCGGTTTCCGAGACGCGACCACACAACCACTCAGCTCGCTCTCTCCACTCGGACTAATTCGCCTC CCGGTTTCCGAGACGCGACCACACAACCACTCCGCTCGCTCTCTCCACTCGGACTAATTCGCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:47176302..47176551;chr2:47176336..47176601 26863196 MeRIP-seq:(Medium) rs781438828 Functional Loss SNV dbSNP153 33..33 33 - - - 109527 RMVar_ID_109527 Human_SNP_ID_70446019 m1A Human chr2 + 47176489 47176489 47176489 CCGGTTTCCGAGACGCGACCACACAACCACTCAGCTCGCTCTCTCCACTCGGACTAATTCGCCTC CCGGTTTCCGAGACGCGACCACACAACCACTCGGCTCGCTCTCTCCACTCGGACTAATTCGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:47176302..47176551;chr2:47176336..47176601 26863196 MeRIP-seq:(Medium) rs781438828 Functional Loss SNV dbSNP153 33..33 33 - - - 109528 RMVar_ID_109528 Human_SNP_ID_70446020 m1A Human chr2 + 47176489 47176489 47176489 CCGGTTTCCGAGACGCGACCACACAACCACTCAGCTCGCTCTCTCCACTCGGACTAATTCGCCTC CCGGTTTCCGAGACGCGACCACACAACCACTCTGCTCGCTCTCTCCACTCGGACTAATTCGCCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:47176302..47176551;chr2:47176336..47176601 26863196 MeRIP-seq:(Medium) rs781438828 Functional Loss SNV dbSNP153 33..33 33 - - - 109529 RMVar_ID_109529 Human_SNP_ID_70493207 m1A Human chr2 + 47335398 47335398 47335398 AGGCGGGAGGATAGCTTGAGCCCAGGAGTTCGAGACCTGCCTGGGCAATATAGCGAGACCCCGTT AGGCGGGAGGATAGCTTGAGCCCAGGAGTTCGCGACCTGCCTGGGCAATATAGCGAGACCCCGTT A C BCYRN1 Ensembl:ENSG00000236824 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1242309013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23892602 109530 RMVar_ID_109530 Human_SNP_ID_70493208 m1A Human chr2 + 47335400 47335400 47335400 GCGGGAGGATAGCTTGAGCCCAGGAGTTCGAGACCTGCCTGGGCAATATAGCGAGACCCCGTTCT GCGGGAGGATAGCTTGAGCCCAGGAGTTCGAGCCCTGCCTGGGCAATATAGCGAGACCCCGTTCT A C BCYRN1 Ensembl:ENSG00000236824 Other exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1445343139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23892602 109531 RMVar_ID_109531 Human_SNP_ID_70516969 m1A Human chr2 - 47403199 47403191 47403199 CGCTCTCCAACTGCAGCGTCTCCTTCGGCTGCACCGCCATGTCGAAACCTCCTCACCTCCTGGTT CGCTCTCCAACTGCAGCGTCTCCTTCGGCTGC________GTCGAAACCTCCTCACCTCCTGGTT CATGGCGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:47403101..47403447;chr2:47403101..47408511;chr2:47403126..47403425 26863196 MeRIP-seq:(Medium) rs1558451013 Functional Loss DEL dbSNP153 33..40 33 - - - 109532 RMVar_ID_109532 Human_SNP_ID_70516974 m1A Human chr2 - 47403193 47403193 47403193 CCAACTGCAGCGTCTCCTTCGGCTGCACCGCCATGTCGAAACCTCCTCACCTCCTGGTTGAAGAA CCAACTGCAGCGTCTCCTTCGGCTGCACCGCCCTGTCGAAACCTCCTCACCTCCTGGTTGAAGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:47403098..47403425 26863196 MeRIP-seq:(Medium) rs876658825 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_714 109533 RMVar_ID_109533 Human_SNP_ID_70516997 m1A Human chr2 - 47403222 47403208 47403223 GCGCACGAAGCCGACCTCGGCCGCGCTCTCCAACTGCAGCGTCTCCTTCGGCTGCACCGCCATGT GCGCACGAAGCCGACCTCGGCCGCGCTCTCC_______________TTCGGCTGCACCGCCATGT AGGAGACGCTGCAGTT A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:47403176..47403375 26863196 MeRIP-seq:(Medium) rs1184949521 Functional Loss DEL dbSNP153 32..46 33 - - - 109534 RMVar_ID_109534 Human_SNP_ID_70517017 m1A Human chr2 - 47403222 47403221 47403222 GCGCACGAAGCCGACCTCGGCCGCGCTCTCCAACTGCAGCGTCTCCTTCGGCTGCACCGCCATGT GCGCACGAAGCCGACCTCGGCCGCGCTCTCCA_CTGCAGCGTCTCCTTCGGCTGCACCGCCATGT GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:47403176..47403375 26863196 MeRIP-seq:(Medium) rs869224712 Functional Loss DEL dbSNP153 33..33 33 - - - 109535 RMVar_ID_109535 Human_SNP_ID_70517047 m1A Human chr2 - 47403247 47403247 47403247 GCTTCTCCGGCATGCCCTGAAAGAAGCGCACGAAGCCGACCTCGGCCGCGCTCTCCAACTGCAGC GCTTCTCCGGCATGCCCTGAAAGAAGCGCACGGAGCCGACCTCGGCCGCGCTCTCCAACTGCAGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr2:47403147..47403297;chr2:47403159..47403252 26863196,26863410 MeRIP-seq:(Medium) rs1320061495 Functional Loss SNV dbSNP153 33..33 33 - - - 109536 RMVar_ID_109536 Human_SNP_ID_70517084 m1A Human chr2 + 47403276 47403276 47403276 GCTTCGTGCGCTTCTTTCAGGGCATGCCGGAGAAGCCGACCACCACAGTGCGCCTTTTCGACCGG GCTTCGTGCGCTTCTTTCAGGGCATGCCGGAGTAGCCGACCACCACAGTGCGCCTTTTCGACCGG A T MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:47403226..47403390 26863196 MeRIP-seq:(Medium) rs1060502001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1587449,Human_RBP_ID_4623290,Human_RBP_ID_6927247,Human_RBP_ID_8848490,Human_RBP_ID_9330453,Human_RBP_ID_9386448,Human_RBP_ID_17957915,Human_RBP_ID_18193286,Human_RBP_ID_18421763,Human_RBP_ID_18761801,Human_RBP_ID_22076243 Clinvar_Rec_715 RMVar_hsa_circ_199607 109537 RMVar_ID_109537 Human_SNP_ID_70517187 m1A Human chr2 - 47403346 47403346 47403346 CCCCCTGGGTCTTGAACACCTCCCGGGCGGCCAGCAGCGCGTCCTCGCCGTGCGCCGTATAGAAG CCCCCTGGGTCTTGAACACCTCCCGGGCGGCCGGCAGCGCGTCCTCGCCGTGCGCCGTATAGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47403301..47403400 32194978 MeRIP-seq:(Medium) rs780840040 Functional Loss SNV dbSNP153 33..33 33 - - - 109538 RMVar_ID_109538 Human_SNP_ID_70520091 m1A Human chr2 - 47410296 47410294 47410297 AAACACATTCCTTTGGTCCAATCTGGATGAGGAGAGCCTCAAGATTGGAGAACTGATCATTATCA AAACACATTCCTTTGGTCCAATCTGGATGAG___AGCCTCAAGATTGGAGAACTGATCATTATCA TCTC T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47410246..47412436 32194978 MeRIP-seq:(Medium) rs587779165 Functional Loss DEL dbSNP153 32..34 33 - - - Clinvar_Rec_716 109539 RMVar_ID_109539 Human_SNP_ID_70520094 m1A Human chr2 - 47410296 47410296 47410297 AAACACATTCCTTTGGTCCAATCTGGATGAGGAGAGCCTCAAGATTGGAGAACTGATCATTATCA AAACACATTCCTTTGGTCCAATCTGGATGAGAGGAGCCTCAAGATTGGAGAACTGATCATTATCA TC CT - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47410246..47412436 32194978 MeRIP-seq:(Medium) rs267607927 Functional Loss MNV dbSNP153 32..33 33 - - - 109540 RMVar_ID_109540 Human_SNP_ID_70520095 m1A Human chr2 - 47410296 47410296 47410296 AAACACATTCCTTTGGTCCAATCTGGATGAGGAGAGCCTCAAGATTGGAGAACTGATCATTATCA AAACACATTCCTTTGGTCCAATCTGGATGAGGGGAGCCTCAAGATTGGAGAACTGATCATTATCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47410246..47412436 32194978 MeRIP-seq:(Medium) rs1114167878 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_717 109541 RMVar_ID_109541 Human_SNP_ID_70545868 m1A Human chr2 - 47476512 47476508 47476512 TCAGCCATGAACGTGGAGACTCCTTTCAATTGACTGTCACCAGCCCCTACTCGGGCTAAGATGCA TCAGCCATGAACGTGGAGACTCCTTTCAATTG____TCACCAGCCCCTACTCGGGCTAAGATGCA ACAGT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47475268..47476513 32194978 MeRIP-seq:(Medium) rs878853809 Functional Loss DEL dbSNP153 33..36 33 - - - Clinvar_Rec_718 109542 RMVar_ID_109542 Human_SNP_ID_70564259 m1A Human chr2 - 47538358 47538357 47538358 CAAACATCCGTTCCTTAACGAGGCCTCCCTGGACCCACCCCACTTAAAACCATGACCTGCCTCCT CAAACATCCGTTCCTTAACGAGGCCTCCCTGG_CCCACCCCACTTAAAACCATGACCTGCCTCCT GT G KCNK12 Ensembl:ENSG00000184261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47538316..47538430 26863196 MeRIP-seq:(Medium) rs932695188 Functional Loss DEL dbSNP153 33..33 33 - - - 109543 RMVar_ID_109543 Human_SNP_ID_70564261 m1A Human chr2 - 47538358 47538358 47538358 CAAACATCCGTTCCTTAACGAGGCCTCCCTGGACCCACCCCACTTAAAACCATGACCTGCCTCCT CAAACATCCGTTCCTTAACGAGGCCTCCCTGGGCCCACCCCACTTAAAACCATGACCTGCCTCCT T C KCNK12 Ensembl:ENSG00000184261 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47538316..47538430 26863196 MeRIP-seq:(Medium) rs565026708 Functional Loss SNV dbSNP153 33..33 33 - - - 109544 RMVar_ID_109544 Human_SNP_ID_70577625 m1A Human chr2 + 47588181 47588181 47588181 ACATCAAGAACGGAATAGTGAGTTGTGGAGGAAGGTATTGAGGACAAAAGAATGTATGGGTTGGG ACATCAAGAACGGAATAGTGAGTTGTGGAGGACGGTATTGAGGACAAAAGAATGTATGGGTTGGG A C MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47588132..47588228 26863196 MeRIP-seq:(Medium) rs1035346196 Functional Loss SNV dbSNP153 33..33 33 - - - 109545 RMVar_ID_109545 Human_SNP_ID_70609011 m1A Human chr2 - 47691192 47691192 47691192 GAGAGTACAAAGTAGTGGGTCGCTGCCTGCCCACCCCCAAATGCCACACACCACCCCTCTACCGC GAGAGTACAAAGTAGTGGGTCGCTGCCTGCCCGCCCCCAAATGCCACACACCACCCCTCTACCGC T C AC079250.1 Ensembl:ENSG00000230979 Pseudogene exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:47691179..47691267 26863410 MeRIP-seq:(Medium) rs1000183485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1828998,Human_miRNA_ID_1893110,Human_miRNA_ID_1901666 109546 RMVar_ID_109546 Human_SNP_ID_70636780 m1A Human chr2 - 47783219 47783219 47783219 GGTGCTCTGTCGCGACATACCGACAGCCGGCAAGGCCCAACCGTTCTGTCGGACGGAGCTCCTAA GGTGCTCTGTCGCGACATACCGACAGCCGGCACGGCCCAACCGTTCTGTCGGACGGAGCTCCTAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:47783168..47783279 26863196 MeRIP-seq:(Medium) - Functional Loss SNV HGVD 33..33 33 - - - 109547 RMVar_ID_109547 Human_SNP_ID_70636817 m1A Human chr2 + 47783249 47783249 47783249 CCTTGCCGGCTGTCGGTATGTCGCGACAGAGCACCCTGTACAGCTTCTTCCCCAAGTCTCCGGCG CCTTGCCGGCTGTCGGTATGTCGCGACAGAGCCCCCTGTACAGCTTCTTCCCCAAGTCTCCGGCG A C MSH6 Ensembl:ENSG00000116062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47783200..47783302 26863196 MeRIP-seq:(Medium) rs200944853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_551974,Human_RBP_ID_1587520,Human_RBP_ID_3627968,Human_RBP_ID_4623292,Human_RBP_ID_5146546,Human_RBP_ID_5423101,Human_RBP_ID_5444907,Human_RBP_ID_5470855,Human_RBP_ID_5502289,Human_RBP_ID_6927721,Human_RBP_ID_8520641,Human_RBP_ID_8848534,Human_RBP_ID_9259711,Human_RBP_ID_9295908,Human_RBP_ID_9330454,Human_RBP_ID_13907660,Human_RBP_ID_18421764,Human_RBP_ID_18761919,Human_RBP_ID_21893624,Human_RBP_ID_27012337 Human_miRNA_ID_2906309,Human_miRNA_ID_3025139 Clinvar_Rec_719 RMVar_hsa_circ_84947,RMVar_hsa_circ_199625 109548 RMVar_ID_109548 Human_SNP_ID_70636855 m1A Human chr2 - 47783290 47783290 47783290 TCGCGTGAGGCCCTGGCCGAGGCCTTGTTGGCATCACTCAGCGCCGGAGACTTGGGGAAGAAGCT TCGCGTGAGGCCCTGGCCGAGGCCTTGTTGGCGTCACTCAGCGCCGGAGACTTGGGGAAGAAGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47783239..47783340 32194978 MeRIP-seq:(Medium) rs752794296 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_720 109549 RMVar_ID_109549 Human_SNP_ID_70637081 m1A Human chr2 + 47783473 47783473 47783473 AAGAACCTCAACGGAGGGCTGCGGAGATCGGTAGCGCCTGCTGCCCCCACCAGGTAGCGGGGTGG AAGAACCTCAACGGAGGGCTGCGGAGATCGGTGGCGCCTGCTGCCCCCACCAGGTAGCGGGGTGG A G MSH6 Ensembl:ENSG00000116062 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47783451..47783475 32194978 MeRIP-seq:(Medium) rs864622281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920180,Human_RBP_ID_8848545,Human_RBP_ID_9296473,Human_RBP_ID_22997340 Human_Splice_Rec_243317,Human_Splice_Rec_243333,Human_Splice_Rec_243349,Human_Splice_Rec_243365,Human_Splice_Rec_243369,Human_Splice_Rec_243371,Human_Splice_Rec_243389,Human_Splice_Rec_243413 Human_miRNA_ID_600257,Human_miRNA_ID_1046539,Human_miRNA_ID_2219697,Human_miRNA_ID_2482736,Human_miRNA_ID_3071110 Clinvar_Rec_721 RMVar_hsa_circ_84947,RMVar_hsa_circ_199625 109550 RMVar_ID_109550 Human_SNP_ID_70637243 m1A Human chr2 - 47783706 47783706 47783706 TCCGCGTCTCCCCTGCAGCCCTCTTCCTGCACAGCCTCTCTCCTCCGACCCTGTTTACAAGCTAC TCCGCGTCTCCCCTGCAGCCCTCTTCCTGCACGGCCTCTCTCCTCCGACCCTGTTTACAAGCTAC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:47783692..47783821 26863196 MeRIP-seq:(Medium) rs1301962972 Functional Loss SNV dbSNP153 33..33 33 - - - 109551 RMVar_ID_109551 Human_SNP_ID_70637390 m1A Human chr2 + 47783982 47783982 47783982 GGGGAGAGTCCGGTGGTGTGGGGTGCGAAAGGAGGTTCCTCGGCCGGCGCGGAGATAGTGAGTTG GGGGAGAGTCCGGTGGTGTGGGGTGCGAAAGGGGGTTCCTCGGCCGGCGCGGAGATAGTGAGTTG A G MSH6 Ensembl:ENSG00000116062 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47783944..47784307 26863196 MeRIP-seq:(Medium) rs549751558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242634,Human_RBP_ID_264190,Human_RBP_ID_3637924,Human_RBP_ID_5322466,Human_RBP_ID_8110179,Human_RBP_ID_8200509,Human_RBP_ID_8233932,Human_RBP_ID_9428643,Human_RBP_ID_17192196,Human_RBP_ID_18949150,Human_RBP_ID_23875007,Human_RBP_ID_26786923 RMVar_hsa_circ_84947,RMVar_hsa_circ_199625 109552 RMVar_ID_109552 Human_SNP_ID_70640019 m1A Human chr2 + 47791001 47791001 47791001 GGGTTACCCCTGGTGGCCTTGTCTGGTTTACAACCACCCCTTTGATGGAACATTCATCCGCGAGA GGGTTACCCCTGGTGGCCTTGTCTGGTTTACACCCACCCCTTTGATGGAACATTCATCCGCGAGA A C MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:47790976..47791000 26863196 MeRIP-seq:(Medium) rs587779934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1587527,Human_RBP_ID_6927772,Human_RBP_ID_8848550,Human_RBP_ID_9296475,Human_RBP_ID_22450300,Human_RBP_ID_22815722 Human_Splice_Rec_243300,Human_Splice_Rec_243318,Human_Splice_Rec_243334,Human_Splice_Rec_243350,Human_Splice_Rec_243372,Human_Splice_Rec_243390,Human_Splice_Rec_243396,Human_Splice_Rec_243430,Human_Splice_Rec_243436,Human_Splice_Rec_243440,Human_Splice_Rec_243458 Clinvar_Rec_722,Clinvar_Rec_723 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_296979,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_199628 109553 RMVar_ID_109553 Human_SNP_ID_70640020 m1A Human chr2 + 47791001 47791001 47791001 GGGTTACCCCTGGTGGCCTTGTCTGGTTTACAACCACCCCTTTGATGGAACATTCATCCGCGAGA GGGTTACCCCTGGTGGCCTTGTCTGGTTTACAGCCACCCCTTTGATGGAACATTCATCCGCGAGA A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:47790976..47791000 26863196 MeRIP-seq:(Medium) rs587779934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1587527,Human_RBP_ID_6927772,Human_RBP_ID_8848550,Human_RBP_ID_9296475,Human_RBP_ID_22450300,Human_RBP_ID_22815722 Human_Splice_Rec_243300,Human_Splice_Rec_243318,Human_Splice_Rec_243334,Human_Splice_Rec_243350,Human_Splice_Rec_243372,Human_Splice_Rec_243390,Human_Splice_Rec_243396,Human_Splice_Rec_243430,Human_Splice_Rec_243436,Human_Splice_Rec_243440,Human_Splice_Rec_243458 Clinvar_Rec_722,Clinvar_Rec_723 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_296979,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_199628 109554 RMVar_ID_109554 Human_SNP_ID_70642105 m1A Human chr2 + 47796045 47796045 47796045 TTGGCAGTTTGTGATGAGCCCTCAGAGCCAGAAGAGGAAGAAGAGATGGAGGTGGGACACGGCAA TTGGCAGTTTGTGATGAGCCCTCAGAGCCAGAGGAGGAAGAAGAGATGGAGGTGGGACACGGCAA A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47795995..47796113 26863196 MeRIP-seq:(Medium) rs536686679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1587532,Human_RBP_ID_1919067,Human_RBP_ID_6927794,Human_RBP_ID_8851188,Human_RBP_ID_9383612,Human_RBP_ID_19097377,Human_RBP_ID_21982212,Human_RBP_ID_22076244,Human_RBP_ID_23115021,Human_RBP_ID_24546043,Human_RBP_ID_26339267 Human_Splice_Rec_243303,Human_Splice_Rec_243337,Human_Splice_Rec_243367,Human_Splice_Rec_243375,Human_Splice_Rec_243393,Human_Splice_Rec_243399,Human_Splice_Rec_243433,Human_Splice_Rec_243443,Human_Splice_Rec_243461 Clinvar_Rec_724 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_296979,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_199628,RMVar_hsa_circ_109544,RMVar_hsa_circ_308356,RMVar_hsa_circ_199629,RMVar_hsa_circ_199630 109555 RMVar_ID_109555 Human_SNP_ID_70642109 m1A Human chr2 + 47796054 47796054 47796054 TGTGATGAGCCCTCAGAGCCAGAAGAGGAAGAAGAGATGGAGGTGGGACACGGCAAGCATTCAGT TGTGATGAGCCCTCAGAGCCAGAAGAGGAAGAGGAGATGGAGGTGGGACACGGCAAGCATTCAGT A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:47795852..47796109;chr2:47795926..47796096 26863196 MeRIP-seq:(Medium) rs758635514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919067,Human_RBP_ID_6927794,Human_RBP_ID_8851188,Human_RBP_ID_9383612,Human_RBP_ID_19097377,Human_RBP_ID_21982212,Human_RBP_ID_22076244,Human_RBP_ID_23115021,Human_RBP_ID_24546043,Human_RBP_ID_26339267 Human_Splice_Rec_243303,Human_Splice_Rec_243337,Human_Splice_Rec_243367,Human_Splice_Rec_243375,Human_Splice_Rec_243393,Human_Splice_Rec_243399,Human_Splice_Rec_243433,Human_Splice_Rec_243443,Human_Splice_Rec_243461 Clinvar_Rec_725 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_296979,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_199628,RMVar_hsa_circ_109544,RMVar_hsa_circ_308356,RMVar_hsa_circ_199629,RMVar_hsa_circ_199630 109556 RMVar_ID_109556 Human_SNP_ID_70642996 m1A Human chr2 + 47798684 47798684 47798684 TGAAATTGAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAA TGAAATTGAGAGTGAAGAGGAAGTACAGCCTACGACACAAGGATCTAGGCGAAGTAGCCGCCAAA A C MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:47798597..47798800 26863196 MeRIP-seq:(Medium) rs1558658986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828612,Human_RBP_ID_923781,Human_RBP_ID_1919073,Human_RBP_ID_2649652,Human_RBP_ID_6927810,Human_RBP_ID_8848555,Human_RBP_ID_17657574,Human_RBP_ID_23114987,Human_RBP_ID_24545785,Human_RBP_ID_26339270,Human_RBP_ID_26770145,Human_RBP_ID_27480459,Human_RBP_ID_27817065 Human_Splice_Rec_243304,Human_Splice_Rec_243320,Human_Splice_Rec_243338,Human_Splice_Rec_243352,Human_Splice_Rec_243368,Human_Splice_Rec_243370,Human_Splice_Rec_243376,Human_Splice_Rec_243394,Human_Splice_Rec_243400,Human_Splice_Rec_243416,Human_Splice_Rec_243434,Human_Splice_Rec_243444,Human_Splice_Rec_243462 Clinvar_Rec_726,Clinvar_Rec_7686 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_351635,RMVar_hsa_circ_199631 109557 RMVar_ID_109557 Human_SNP_ID_70643002 m1A Human chr2 + 47798691 47798691 47798691 GAGAGTGAAGAGGAAGTACAGCCTAAGACACAAGGATCTAGGCGAAGTAGCCGCCAAATAAAAAA GAGAGTGAAGAGGAAGTACAGCCTAAGACACATGGATCTAGGCGAAGTAGCCGCCAAATAAAAAA A T MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47798601..47798900 26863196 MeRIP-seq:(Medium) rs1322117538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_923781,Human_RBP_ID_1587533,Human_RBP_ID_1919073,Human_RBP_ID_6927811,Human_RBP_ID_8848555,Human_RBP_ID_17657574,Human_RBP_ID_23114987,Human_RBP_ID_24545785,Human_RBP_ID_26339270,Human_RBP_ID_26770145,Human_RBP_ID_27817065 Human_Splice_Rec_243304,Human_Splice_Rec_243320,Human_Splice_Rec_243338,Human_Splice_Rec_243352,Human_Splice_Rec_243368,Human_Splice_Rec_243370,Human_Splice_Rec_243376,Human_Splice_Rec_243394,Human_Splice_Rec_243400,Human_Splice_Rec_243416,Human_Splice_Rec_243434,Human_Splice_Rec_243444,Human_Splice_Rec_243462 Clinvar_Rec_727 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_351635,RMVar_hsa_circ_199631 109558 RMVar_ID_109558 Human_SNP_ID_70643697 m1A Human chr2 - 47799458 47799458 47799458 ATATATGTGCCATCTTTCTACATCGTGCCTCCATCATTTCTGGAGTCTCAGTCTGTTCCACTCGT ATATATGTGCCATCTTTCTACATCGTGCCTCCGTCATTTCTGGAGTCTCAGTCTGTTCCACTCGT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:47799409..47799482 26863196 MeRIP-seq:(Medium) rs1558661808 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_728 109559 RMVar_ID_109559 Human_SNP_ID_70643953 m1A Human chr2 + 47799746 47799746 47799746 CCATTGTTCGAGATTTAGGACTCTAGTGGCACACTATCCCCCAGTACAAGTTTTATTTGAAAAAG CCATTGTTCGAGATTTAGGACTCTAGTGGCACGCTATCCCCCAGTACAAGTTTTATTTGAAAAAG A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47799695..47799796 32194978 MeRIP-seq:(Medium) rs786202725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919086,Human_RBP_ID_6927835,Human_RBP_ID_8108557,Human_RBP_ID_8848583,Human_RBP_ID_9259713,Human_RBP_ID_9295922,Human_RBP_ID_13908085,Human_RBP_ID_22764988,Human_RBP_ID_27290735,Human_RBP_ID_27696566 Human_miRNA_ID_2652904,Human_miRNA_ID_2754099 Clinvar_Rec_729 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_351635,RMVar_hsa_circ_199631 109560 RMVar_ID_109560 Human_SNP_ID_70646459 m1A Human chr2 + 47803529 47803529 47803529 GATACCCCCCCCTTCTTAGAGCTTAAAGGATCACGCCATCCTTGCATTACGAAGACTTTTTTTGG GATACCCCCCCCTTCTTAGAGCTTAAAGGATCTCGCCATCCTTGCATTACGAAGACTTTTTTTGG A T MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47803481..47804948 32194978 MeRIP-seq:(Medium) rs372996269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58289,Human_RBP_ID_1919125,Human_RBP_ID_8848641,Human_RBP_ID_9259998,Human_RBP_ID_9295938,Human_RBP_ID_18761971,Human_RBP_ID_22452190,Human_RBP_ID_22993411,Human_RBP_ID_23875073,Human_RBP_ID_27696590 Clinvar_Rec_730 RMVar_hsa_circ_35044,RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_62749,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_199631,RMVar_hsa_circ_367415 109561 RMVar_ID_109561 Human_SNP_ID_70648122 m1A Human chr2 + 47806352 47806352 47806352 GATTATTCTCAAAATGTTGCTGTGCGCCTAGGACATATGGTATGTGCAAATTGTTTTTTTCCACA GATTATTCTCAAAATGTTGCTGTGCGCCTAGGGCATATGGTATGTGCAAATTGTTTTTTTCCACA A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47806283..47806527 32194978 MeRIP-seq:(Medium) rs786202166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919133,Human_RBP_ID_8848664,Human_RBP_ID_13908356,Human_RBP_ID_18761983,Human_RBP_ID_23875082 Human_Splice_Rec_243313,Human_Splice_Rec_243329,Human_Splice_Rec_243345,Human_Splice_Rec_243361,Human_Splice_Rec_243385,Human_Splice_Rec_243409,Human_Splice_Rec_243425,Human_Splice_Rec_243453 Human_miRNA_ID_3012803 Clinvar_Rec_731 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_199625,RMVar_hsa_circ_62749,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_199631,RMVar_hsa_circ_367415,RMVar_hsa_circ_95766,RMVar_hsa_circ_101186,RMVar_hsa_circ_101970,RMVar_hsa_circ_199632,RMVar_hsa_circ_199633,RMVar_hsa_circ_199634 109562 RMVar_ID_109562 Human_SNP_ID_70684155 m1A Human chr2 - 47905593 47905593 47905593 GCCGCAGCCGCCCCAGCAGCAGCCGCCCCAGCAGCAGCCTCCGCCGCCGCCGCAGCAGCAGCAGC GCCGCAGCCGCCCCAGCAGCAGCCGCCCCAGCTGCAGCCTCCGCCGCCGCCGCAGCAGCAGCAGC T A FBXO11 Ensembl:ENSG00000138081 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47905543..47906867 26863196 MeRIP-seq:(Medium) rs776045501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533527 109563 RMVar_ID_109563 Human_SNP_ID_70684156 m1A Human chr2 - 47905593 47905593 47905593 GCCGCAGCCGCCCCAGCAGCAGCCGCCCCAGCAGCAGCCTCCGCCGCCGCCGCAGCAGCAGCAGC GCCGCAGCCGCCCCAGCAGCAGCCGCCCCAGCCGCAGCCTCCGCCGCCGCCGCAGCAGCAGCAGC T G FBXO11 Ensembl:ENSG00000138081 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:47905543..47906867 26863196 MeRIP-seq:(Medium) rs776045501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22533527 109564 RMVar_ID_109564 Human_SNP_ID_70684258 m1A Human chr2 - 47905743 47905743 47905743 CTGTGCGTGTGCGTGTGTGTGTCCCTCCGCCAACGCCGCCACCTCAGCCCGGCAAATGAACTCCG CTGTGCGTGTGCGTGTGTGTGTCCCTCCGCCAGCGCCGCCACCTCAGCCCGGCAAATGAACTCCG T C FBXO11 Ensembl:ENSG00000138081 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:47905647..47906074 26863196 MeRIP-seq:(Medium) rs1237518780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243707,Human_RBP_ID_4610960,Human_RBP_ID_5131570,Human_RBP_ID_17084496,Human_RBP_ID_17569258,Human_RBP_ID_18949153,Human_RBP_ID_22533575 109565 RMVar_ID_109565 Human_SNP_ID_70684348 m1A Human chr2 + 47905823 47905819 47905823 GAGAAAGGGGTGGGGAGAGTGGGAGAGGGGGGAGGAAGGAGAGGGGGCGAGGGGAAGGGGAGACG GAGAAAGGGGTGGGGAGAGTGGGAGAGGG____GGAAGGAGAGGGGGCGAGGGGAAGGGGAGACG GGGGA G AC079807.1 Ensembl:ENSG00000233230 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47905772..47906150 32194978 MeRIP-seq:(Medium) rs1038636353 Functional Loss DEL dbSNP153 30..33 33 - - - 109566 RMVar_ID_109566 Human_SNP_ID_70684484 m1A Human chr2 + 47906030 47906030 47906030 GCAGAAAGACGGGCAGACCGAGAGAAAGAAAGAAAGGGCGTCCGCCGCTTGGGGATCCCGAGGCG GCAGAAAGACGGGCAGACCGAGAGAAAGAAAGGAAGGGCGTCCGCCGCTTGGGGATCCCGAGGCG A G AC079807.1 Ensembl:ENSG00000233230 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:47905549..47906867 26863196 MeRIP-seq:(Medium) rs988951410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5591810 109567 RMVar_ID_109567 Human_SNP_ID_70832391 m1A Human chr2 + 48440850 48440850 48440850 GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCAGGCAGATACTGCCTGACCCGTTCCCGGGAGCG GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCGGGCAGATACTGCCTGACCCGTTCCCGGGAGCG A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:48440800..48441135 26863196 MeRIP-seq:(Medium) rs903578326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421767 109568 RMVar_ID_109568 Human_SNP_ID_70832392 m1A Human chr2 + 48440850 48440850 48440850 GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCAGGCAGATACTGCCTGACCCGTTCCCGGGAGCG GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCTGGCAGATACTGCCTGACCCGTTCCCGGGAGCG A T PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:48440800..48441135 26863196 MeRIP-seq:(Medium) rs903578326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18421767 109569 RMVar_ID_109569 Human_SNP_ID_70832399 m1A Human chr2 + 48440866 48440866 48440866 GCTGCGGTGGCCAAGCAGGCAGATACTGCCTGACCCGTTCCCGGGAGCGTGTCTGGGTTTGGGGG GCTGCGGTGGCCAAGCAGGCAGATACTGCCTGTCCCGTTCCCGGGAGCGTGTCTGGGTTTGGGGG A T PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:48440817..48441135 26863196 MeRIP-seq:(Medium) rs991106897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_552076,Human_RBP_ID_4622396,Human_RBP_ID_18422200,Human_RBP_ID_18443608 109570 RMVar_ID_109570 Human_SNP_ID_70839680 m1A Human chr2 + 48464347 48464347 48464347 AAGGGCAGGTTTGAGTGGCTGAAGGGATGAGTAGAGATGAGGAGAGATGCAGCTCATTAAGGAGG AAGGGCAGGTTTGAGTGGCTGAAGGGATGAGTGGAGATGAGGAGAGATGCAGCTCATTAAGGAGG A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:48464179..48464498 26863196 MeRIP-seq:(Medium) rs1262902420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_828965,Human_RBP_ID_13909744 RMVar_hsa_circ_273593,RMVar_hsa_circ_342007,RMVar_hsa_circ_328020,RMVar_hsa_circ_284081,RMVar_hsa_circ_289662,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_74315,RMVar_hsa_circ_44269,RMVar_hsa_circ_73510,RMVar_hsa_circ_199692,RMVar_hsa_circ_199694,RMVar_hsa_circ_199695,RMVar_hsa_circ_199693,RMVar_hsa_circ_199691,RMVar_hsa_circ_348660,RMVar_hsa_circ_363706,RMVar_hsa_circ_57601,RMVar_hsa_circ_199696,RMVar_hsa_circ_199697,RMVar_hsa_circ_12781,RMVar_hsa_circ_51467,RMVar_hsa_circ_68225,RMVar_hsa_circ_285633,RMVar_hsa_circ_199698,RMVar_hsa_circ_199701,RMVar_hsa_circ_312091 109571 RMVar_ID_109571 Human_SNP_ID_72353327 m1A Human chr2 - 53495730 53495730 53495730 GAGGTGGTCCAGGCAGAGGAAGATGTGCCTTTAGAGAAGCAGTACAGAGACCAGCCAGAGAAGTT GAGGTGGTCCAGGCAGAGGAAGATGTGCCTTTGGAGAAGCAGTACAGAGACCAGCCAGAGAAGTT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:53495686..53495804 26863196 MeRIP-seq:(Medium) rs1043188620 Functional Loss SNV dbSNP153 33..33 33 - - - 109572 RMVar_ID_109572 Human_SNP_ID_72355733 m1A Human chr2 + 53504956 53504956 53504956 AGAACCCCCATCTCCAGGCCTGACTTTGGACTATTTACCTGCATGCAAACACTTTCCCAACTCTA AGAACCCCCATCTCCAGGCCTGACTTTGGACTGTTTACCTGCATGCAAACACTTTCCCAACTCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:53504905..53505043 26863196 MeRIP-seq:(Medium) rs150340061 Functional Loss SNV dbSNP153 33..33 33 - - - 109573 RMVar_ID_109573 Human_SNP_ID_72406571 m1A Human chr2 + 53679018 53679018 53679018 CCACACCCAATCTTTAACATCATGGAGACCTCAGGTCCCAACTCCTCCCCTATCTCATCCTTCAG CCACACCCAATCTTTAACATCATGGAGACCTCGGGTCCCAACTCCTCCCCTATCTCATCCTTCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:53679005..53679125 26863196 MeRIP-seq:(Medium) rs1226487151 Functional Loss SNV dbSNP153 33..33 33 - - - 109574 RMVar_ID_109574 Human_SNP_ID_72432324 m1A Human chr2 - 53767890 53767890 53767890 CTTCCAGATCAGGGACCCGTAACCAAAAACCCACATCTTCTCGCGGCTCCTCTGCCCCAGTGGCC CTTCCAGATCAGGGACCCGTAACCAAAAACCCGCATCTTCTCGCGGCTCCTCTGCCCCAGTGGCC T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:53767840..53768017;chr2:53767840..53774222 26863196 MeRIP-seq:(Medium) rs1288175097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199815 109575 RMVar_ID_109575 Human_SNP_ID_72491152 m1A Human chr2 - 53970696 53970694 53970697 CGAGCCGGGCCCGCGGGGCTTCGTCCCGCAGAAGGAGATCGTCTACAACAAGCTGCTGCCCTACG CGAGCCGGGCCCGCGGGGCTTCGTCCCGCAG___GAGATCGTCTACAACAAGCTGCTGCCCTACG CCTT C PSME4 Ensembl:ENSG00000068878 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:53970647..53970775 26863196 MeRIP-seq:(Medium) rs1371229485 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_204811,Human_RBP_ID_264192,Human_RBP_ID_3637933,Human_RBP_ID_3957835,Human_RBP_ID_4611325,Human_RBP_ID_5146547,Human_RBP_ID_5196382,Human_RBP_ID_5322070,Human_RBP_ID_5471240,Human_RBP_ID_5528531,Human_RBP_ID_8201477,Human_RBP_ID_8234332,Human_RBP_ID_8851212,Human_RBP_ID_8942572,Human_RBP_ID_9296505,Human_RBP_ID_9428649,Human_RBP_ID_13914124,Human_RBP_ID_18421770,Human_RBP_ID_18762302,Human_RBP_ID_18949164,Human_RBP_ID_19001636,Human_RBP_ID_22078070,Human_RBP_ID_22449798,Human_RBP_ID_22595309,Human_RBP_ID_22996807,Human_RBP_ID_23114890,Human_RBP_ID_23119412,Human_RBP_ID_24546438,Human_RBP_ID_26770146 RMVar_hsa_circ_92924,RMVar_hsa_circ_199836 109576 RMVar_ID_109576 Human_SNP_ID_72491200 m1A Human chr2 + 53970759 53970759 53970759 CGGGACGCCCGCCCGGCTCCGGGGGCTCTCCGACTCCCGCCCGCTCGGCCGGCTCCATGAGCCCA CGGGACGCCCGCCCGGCTCCGGGGGCTCTCCGTCTCCCGCCCGCTCGGCCGGCTCCATGAGCCCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:53970631..53970800 26863196 MeRIP-seq:(Medium) rs1402856829 Functional Loss SNV dbSNP153 33..33 33 - - - 109577 RMVar_ID_109577 Human_SNP_ID_72491278 m1A Human chr2 - 53970873 53970873 53970873 GAGGGCGACGGGCCGCCAGCGGCCGCAGGGCGACGAAGACGCGGAGGAGGCGGAGCCCGGAGAGG GAGGGCGACGGGCCGCCAGCGGCCGCAGGGCGGCGAAGACGCGGAGGAGGCGGAGCCCGGAGAGG T C PSME4 Ensembl:ENSG00000068878 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:53970631..53971050;chr2:53970826..53971037 26863196 MeRIP-seq:(Medium) rs1247637063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4611334 109578 RMVar_ID_109578 Human_SNP_ID_72533002 m1A Human chr2 + 54115644 54115644 54115644 CCCATGTGTCCCCTCCCTCTCGCAGCCGCCGCAGTCGCTGCGCCCCGAGCCCCTCTCCGGCTCCT CCCATGTGTCCCCTCCCTCTCGCAGCCGCCGCGGTCGCTGCGCCCCGAGCCCCTCTCCGGCTCCT A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:54115523..54115659 26863196 MeRIP-seq:(Medium) rs1424439351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337102 109579 RMVar_ID_109579 Human_SNP_ID_72533010 m1A Human chr2 + 54115659 54115659 54115659 CCTCTCGCAGCCGCCGCAGTCGCTGCGCCCCGAGCCCCTCTCCGGCTCCTCAACAGAGGGCTCGC CCTCTCGCAGCCGCCGCAGTCGCTGCGCCCCGCGCCCCTCTCCGGCTCCTCAACAGAGGGCTCGC A C ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:54115364..54115845;chr2:54115487..54115839;chr2:54115424..54115826 26863196 MeRIP-seq:(Medium) rs765081368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_245649,Human_Splice_Rec_245655,Human_Splice_Rec_245663,Human_Splice_Rec_245669 RMVar_hsa_circ_337102 109580 RMVar_ID_109580 Human_SNP_ID_72533038 m1A Human chr2 + 54115705 54115705 54115705 TCCTCAACAGAGGGCTCGCCGCCGCCATGTCTACCGCCCAGTCACTCAAATCCGTGGACTACGAG TCCTCAACAGAGGGCTCGCCGCCGCCATGTCTGCCGCCCAGTCACTCAAATCCGTGGACTACGAG A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:54115602..54115737 26863196 MeRIP-seq:(Medium) rs369283207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4611364 Human_Splice_Rec_245649,Human_Splice_Rec_245655,Human_Splice_Rec_245663,Human_Splice_Rec_245669 RMVar_hsa_circ_337102 109581 RMVar_ID_109581 Human_SNP_ID_72624995 m1A Human chr2 + 54456378 54456370 54456379 TCTCCTCCCGGAGCGAGCGCGCAGCCCTGCGCAGCAGCGCCCACTGGTCCCGTCCTGTGAGCCCC TCTCCTCCCGGAGCGAGCGCGCAGC_________CAGCGCCCACTGGTCCCGTCCTGTGAGCCCC CCCTGCGCAG C SPTBN1 Ensembl:ENSG00000115306 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:54456327..54456453;chr2:54456327..54456437 26863196 MeRIP-seq:(Medium) rs1384143576 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_243460,Human_RBP_ID_4622402 109582 RMVar_ID_109582 Human_SNP_ID_72625011 m1A Human chr2 + 54456425 54456425 54456425 TCCCGTCCTGTGAGCCCCGGCCCCAGCCGCGGACAGACCCGCGGAGTCGCCTCCCGGCCCACCCG TCCCGTCCTGTGAGCCCCGGCCCCAGCCGCGGGCAGACCCGCGGAGTCGCCTCCCGGCCCACCCG A G SPTBN1 Ensembl:ENSG00000115306 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:54456338..54456426 26863410 MeRIP-seq:(Medium) rs1472342863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243460,Human_RBP_ID_4611374 Human_Splice_Rec_245743,Human_Splice_Rec_245817 109583 RMVar_ID_109583 Human_SNP_ID_72625050 m1A Human chr2 - 54456520 54456520 54456520 GTTGGCATCTCCCTGCCTCGGGCCCCCTACCTACCTCCCGGGGATGGGGTGGGGGCGCCGGGGTC GTTGGCATCTCCCTGCCTCGGGCCCCCTACCTGCCTCCCGGGGATGGGGTGGGGGCGCCGGGGTC T C HSALNG0014959 RNACentral:URS0000EBD213 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:54456511..54456916;chr2:54456496..54456666 26863196 MeRIP-seq:(Medium) rs1386514682 Functional Loss SNV dbSNP153 33..33 33 - - - 109584 RMVar_ID_109584 Human_SNP_ID_72641311 m1A Human chr2 - 54508599 54508599 54508599 TGGACCAAAGAAAAATCTCCTTCCAGTCTCACAGGCCCATTCTATTCGTCATTTCATAACCTCTT TGGACCAAAGAAAAATCTCCTTCCAGTCTCACGGGCCCATTCTATTCGTCATTTCATAACCTCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:54508593..54508693 26863196 MeRIP-seq:(Medium) rs1015416636 Functional Loss SNV dbSNP153 33..33 33 - - - 109585 RMVar_ID_109585 Human_SNP_ID_72646191 m1A Human chr2 - 54526352 54526352 54526352 CCTTCTTAGAGTTCTATGAGAAAGAAAAGGAAAAACATTTAGACGTCTGAAGTGTATACAGTCCC CCTTCTTAGAGTTCTATGAGAAAGAAAAGGAAGAACATTTAGACGTCTGAAGTGTATACAGTCCC T C AC092839.1 Ensembl:ENSG00000228108 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr2:54526351..54526425;chr2:54526351..54526400 26863196 MeRIP-seq:(Medium) rs1202078304 Functional Loss SNV dbSNP153 33..33 33 - - - 109586 RMVar_ID_109586 Human_SNP_ID_72646211 m1A Human chr2 + 54526422 54526420 54526423 ATGTGGAGGAGCAGCTGAGACAGTTCAAGATGACGACCACAGTAGCCACAGACTATGACAACATT ATGTGGAGGAGCAGCTGAGACAGTTCAAGAT___GACCACAGTAGCCACAGACTATGACAACATT TGAC T SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:54526351..54526475 26863196 MeRIP-seq:(Medium) rs776616419 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1919540,Human_RBP_ID_8848785 Human_Splice_Rec_245744,Human_Splice_Rec_245818,Human_Splice_Rec_245884,Human_Splice_Rec_245910 RMVar_hsa_circ_14578,RMVar_hsa_circ_59575,RMVar_hsa_circ_311848,RMVar_hsa_circ_357360,RMVar_hsa_circ_123840,RMVar_hsa_circ_19749,RMVar_hsa_circ_199892,RMVar_hsa_circ_199893 109587 RMVar_ID_109587 Human_SNP_ID_72654483 m1A Human chr2 - 54558729 54558727 54558729 CCCGGAGGACTGCGCCCTGGAAATCTCGCTCCAGCCCCCTCCCACTCCCATCCAACACGCAGCAG CCCGGAGGACTGCGCCCTGGAAATCTCGCTCC__CCCCCTCCCACTCCCATCCAACACGCAGCAG GCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr2:54558678..54558826;chr2:54558711..54558812 26863196,32194978 MeRIP-seq:(Medium) rs1240078808 Functional Loss DEL dbSNP153 33..34 33 - - - 109588 RMVar_ID_109588 Human_SNP_ID_72674052 m1A Human chr2 - 54624901 54624901 54624901 GCCAAGTCTCCCTCATAGCTGCCTTGCGATCAAATCTGCGGGCGAGCTGTTCCAGTTTCTCCTGT GCCAAGTCTCCCTCATAGCTGCCTTGCGATCAGATCTGCGGGCGAGCTGTTCCAGTTTCTCCTGT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:54624876..54624900 32194978 MeRIP-seq:(Medium) rs538707375 Functional Loss SNV dbSNP153 33..33 33 - - - 109589 RMVar_ID_109589 Human_SNP_ID_72675026 m1A Human chr2 + 54628227 54628227 54628227 AGAGCGGGTGAGAGGTGTCAATGCCTCCGCCCAGAAGTTCGCAACAGACGGGGAAGGTAAGGATG AGAGCGGGTGAGAGGTGTCAATGCCTCCGCCCGGAAGTTCGCAACAGACGGGGAAGGTAAGGATG A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:54628176..54628275 26863196 MeRIP-seq:(Medium) rs1021178537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242117,Human_RBP_ID_921991,Human_RBP_ID_8851221,Human_RBP_ID_9296513,Human_RBP_ID_9383672,Human_RBP_ID_22076271,Human_RBP_ID_26340886,Human_RBP_ID_27817106 Human_Splice_Rec_245767,Human_Splice_Rec_245841,Human_Splice_Rec_245907,Human_Splice_Rec_245933 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905 109590 RMVar_ID_109590 Human_SNP_ID_72675262 m1A Human chr2 + 54628908 54628907 54628908 CCTGCACCCATGCTGAGCTCCCTCACACAGCCACGTTCCTTCCTTGATGTTAAACAGGTTACAAG CCTGCACCCATGCTGAGCTCCCTCACACAGCC_CGTTCCTTCCTTGATGTTAAACAGGTTACAAG CA C SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54628904..54629236 26863196 MeRIP-seq:(Medium) rs1558444491 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905 109591 RMVar_ID_109591 Human_SNP_ID_72675272 m1A Human chr2 + 54628928 54628928 54628928 CCTCACACAGCCACGTTCCTTCCTTGATGTTAAACAGGTTACAAGCCCTGTGACCCCCAGGTGAT CCTCACACAGCCACGTTCCTTCCTTGATGTTATACAGGTTACAAGCCCTGTGACCCCCAGGTGAT A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:54628926..54629000;chr2:54628926..54629225;chr2:54628926..54629030 26863196 MeRIP-seq:(Medium) rs890018270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22993611 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905 109592 RMVar_ID_109592 Human_SNP_ID_72675273 m1A Human chr2 + 54628929 54628929 54628929 CTCACACAGCCACGTTCCTTCCTTGATGTTAAACAGGTTACAAGCCCTGTGACCCCCAGGTGATC CTCACACAGCCACGTTCCTTCCTTGATGTTAATCAGGTTACAAGCCCTGTGACCCCCAGGTGATC A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:54628926..54629327 26863196 MeRIP-seq:(Medium) rs1365452724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22993611 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905 109593 RMVar_ID_109593 Human_SNP_ID_72675521 m1A Human chr2 + 54629590 54629590 54629590 CGCCCTCCCCCAGGAGCATGCCGAGTCTCCAGACGTGAGGGGCAGGCTGTCGGGCATCGAGGAGC CGCCCTCCCCCAGGAGCATGCCGAGTCTCCAGTCGTGAGGGGCAGGCTGTCGGGCATCGAGGAGC A T SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54629539..54629704 26863196 MeRIP-seq:(Medium) rs1451568073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4611546,Human_RBP_ID_8848833,Human_RBP_ID_9296523,Human_RBP_ID_22450312,Human_RBP_ID_22720653,Human_RBP_ID_22993617 Human_miRNA_ID_2150529,Human_miRNA_ID_2150530,Human_miRNA_ID_2419023,Human_miRNA_ID_2419024,Human_miRNA_ID_2791525,Human_miRNA_ID_2791526 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_111082,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905,RMVar_hsa_circ_199906,RMVar_hsa_circ_199907 109594 RMVar_ID_109594 Human_SNP_ID_72675978 m1A Human chr2 + 54631077 54631077 54631077 GGCATGGAGCGGGACTTGGTGGCCATTGAGGCAAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA GGCATGGAGCGGGACTTGGTGGCCATTGAGGCGAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:54630862..54632715 32194978 MeRIP-seq:(Medium) rs61730127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919580,Human_RBP_ID_8848846 Human_miRNA_ID_2513858,Human_miRNA_ID_2513859,Human_miRNA_ID_2995912,Human_miRNA_ID_2995913 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_111082,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909 109595 RMVar_ID_109595 Human_SNP_ID_72675979 m1A Human chr2 + 54631077 54631077 54631077 GGCATGGAGCGGGACTTGGTGGCCATTGAGGCAAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA GGCATGGAGCGGGACTTGGTGGCCATTGAGGCTAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA A T SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:54630862..54632715 32194978 MeRIP-seq:(Medium) rs61730127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919580,Human_RBP_ID_8848846 Human_miRNA_ID_2513858,Human_miRNA_ID_2513859,Human_miRNA_ID_2995912,Human_miRNA_ID_2995913 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_111082,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909 109596 RMVar_ID_109596 Human_SNP_ID_72680770 m1A Human chr2 + 54646255 54646255 54646255 GCCTCGCATTGACGACATCTTTGAGAGGAGCCAAAACATCGTCACTGACAGCAGCAGCCTCAGCG GCCTCGCATTGACGACATCTTTGAGAGGAGCCGAAACATCGTCACTGACAGCAGCAGCCTCAGCG A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:54646201..54646412 26863196 MeRIP-seq:(Medium) rs768677480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919601,Human_RBP_ID_8848886,Human_RBP_ID_9383743,Human_RBP_ID_18762363 Human_Splice_Rec_245788,Human_Splice_Rec_245858,Human_Splice_Rec_245950 RMVar_hsa_circ_59575,RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_199905,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_68989,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_199916 109597 RMVar_ID_109597 Human_SNP_ID_72681026 m1A Human chr2 + 54647096 54647096 54647096 CTGTCACTCCTTAAGGGGTAGGGCCAGAGGGGACCGCTATGGTTGTGATGTTCTCCTGTCTTTGC CTGTCACTCCTTAAGGGGTAGGGCCAGAGGGGTCCGCTATGGTTGTGATGTTCTCCTGTCTTTGC A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:54647091..54647275 26863196 MeRIP-seq:(Medium) rs752186828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22548245 RMVar_hsa_circ_59575,RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_199905,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_68989,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_199916 109598 RMVar_ID_109598 Human_SNP_ID_72681031 m1A Human chr2 + 54647102 54647102 54647102 CTCCTTAAGGGGTAGGGCCAGAGGGGACCGCTATGGTTGTGATGTTCTCCTGTCTTTGCAGGATG CTCCTTAAGGGGTAGGGCCAGAGGGGACCGCTGTGGTTGTGATGTTCTCCTGTCTTTGCAGGATG A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54647098..54647206 26863196 MeRIP-seq:(Medium) rs756983245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22548245 RMVar_hsa_circ_59575,RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_199905,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_68989,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_199916 109599 RMVar_ID_109599 Human_SNP_ID_72681633 m1A Human chr2 + 54649151 54649151 54649151 GAGCAGTGGATCGCTGAGAGGGAGGTGGTCGCAGGGTCCCATGAACTGGGACAGGACTATGAGCA GAGCAGTGGATCGCTGAGAGGGAGGTGGTCGCGGGGTCCCATGAACTGGGACAGGACTATGAGCA A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:54649025..54649216;chr2:54649101..54649175;chr2:54649001..54649207;chr2:54648976..54649212 26863196 MeRIP-seq:(Medium) rs1391792903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57185,Human_RBP_ID_552304,Human_RBP_ID_775097,Human_RBP_ID_829481,Human_RBP_ID_920126,Human_RBP_ID_8851250,Human_RBP_ID_9259747,Human_RBP_ID_9296539,Human_RBP_ID_9383755,Human_RBP_ID_19097435,Human_RBP_ID_22450323,Human_RBP_ID_22993652,Human_RBP_ID_26338554 Human_Splice_Rec_245793 RMVar_hsa_circ_59575,RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_199904,RMVar_hsa_circ_4264,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_68989,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_87065,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_100796,RMVar_hsa_circ_199916,RMVar_hsa_circ_77244,RMVar_hsa_circ_199917,RMVar_hsa_circ_199918,RMVar_hsa_circ_199919,RMVar_hsa_circ_199920 109600 RMVar_ID_109600 Human_SNP_ID_72681904 m1A Human chr2 - 54649958 54649958 54649958 CCTGTGTGCCCAGAGCCTGGATGTCATGCTCAAATGTAGTGTGCATTCTCTGTAAGGTCTCCACT CCTGTGTGCCCAGAGCCTGGATGTCATGCTCAGATGTAGTGTGCATTCTCTGTAAGGTCTCCACT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:54649908..54652537 32194978 MeRIP-seq:(Medium) rs1181731851 Functional Loss SNV dbSNP153 33..33 33 - - - 109601 RMVar_ID_109601 Human_SNP_ID_72683449 m1A Human chr2 - 54655196 54655196 54655196 AAAGCAAAGTAGCAACCTACCTCCTCAGATGCATAGTGTTTTCTCGCCAACAGGGATTTCCCAAG AAAGCAAAGTAGCAACCTACCTCCTCAGATGCGTAGTGTTTTCTCGCCAACAGGGATTTCCCAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54655146..54655255 26863196 MeRIP-seq:(Medium) rs1237682274 Functional Loss SNV dbSNP153 33..33 33 - - - 109602 RMVar_ID_109602 Human_SNP_ID_72684309 m1A Human chr2 + 54657913 54657913 54657913 CAGTGTGGCCGAGGCCTGGCTGCTTGGACAGGAGCCGTACCTATCCAGCCGAGAGATAGGCCAGA CAGTGTGGCCGAGGCCTGGCTGCTTGGACAGGTGCCGTACCTATCCAGCCGAGAGATAGGCCAGA A T SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54657822..54658086 26863196 MeRIP-seq:(Medium) rs1319106079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242450,Human_RBP_ID_775102,Human_RBP_ID_8851259,Human_RBP_ID_9259750,Human_RBP_ID_9297248,Human_RBP_ID_9383772,Human_RBP_ID_26339317 Human_Splice_Rec_245804,Human_Splice_Rec_245870,Human_Splice_Rec_245962,Human_Splice_Rec_245972 Human_miRNA_ID_1999441,Human_miRNA_ID_1999442 RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_199904,RMVar_hsa_circ_87751,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_87065,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_100796,RMVar_hsa_circ_199916,RMVar_hsa_circ_77244,RMVar_hsa_circ_97546,RMVar_hsa_circ_199917,RMVar_hsa_circ_199918,RMVar_hsa_circ_199919,RMVar_hsa_circ_113664,RMVar_hsa_circ_80058,RMVar_hsa_circ_199922,RMVar_hsa_circ_199923,RMVar_hsa_circ_199921,RMVar_hsa_circ_90114,RMVar_hsa_circ_85457,RMVar_hsa_circ_199925,RMVar_hsa_circ_199926,RMVar_hsa_circ_120851,RMVar_hsa_circ_199927,RMVar_hsa_circ_326303,RMVar_hsa_circ_199928 109603 RMVar_ID_109603 Human_SNP_ID_72684903 m1A Human chr2 + 54659996 54659996 54659996 CAAAACGGTTTGCCAGCTGAACAGGGATCTCCACGGGTTAGTTACCGCTCTCAAACCTACCAAAA CAAAACGGTTTGCCAGCTGAACAGGGATCTCCGCGGGTTAGTTACCGCTCTCAAACCTACCAAAA A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:54659919..54660049;chr2:54659926..54660000 26863196 MeRIP-seq:(Medium) rs751520301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_922032,Human_RBP_ID_9383783,Human_RBP_ID_18317764,Human_RBP_ID_19100252 Human_Splice_Rec_245808,Human_Splice_Rec_245809,Human_Splice_Rec_245874,Human_Splice_Rec_245875,Human_Splice_Rec_245966,Human_Splice_Rec_245976 Human_miRNA_ID_1983879,Human_miRNA_ID_1983880,Human_miRNA_ID_2939518,Human_miRNA_ID_2939519 RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_199904,RMVar_hsa_circ_87751,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_100796,RMVar_hsa_circ_77244,RMVar_hsa_circ_199918,RMVar_hsa_circ_199919,RMVar_hsa_circ_113664,RMVar_hsa_circ_80058,RMVar_hsa_circ_199922,RMVar_hsa_circ_199921,RMVar_hsa_circ_85457,RMVar_hsa_circ_199925,RMVar_hsa_circ_199926,RMVar_hsa_circ_120851,RMVar_hsa_circ_199928 109604 RMVar_ID_109604 Human_SNP_ID_72685156 m1A Human chr2 - 54660830 54660830 54660830 CCTGCCGCGTCCCACGTGCCAGCAGCACTGACAGGGAGCGAGACAGAGGTGGCGGCAGCAGTCAG CCTGCCGCGTCCCACGTGCCAGCAGCACTGACGGGGAGCGAGACAGAGGTGGCGGCAGCAGTCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:54660827..54661027 32194978 MeRIP-seq:(Medium) rs574821017 Functional Loss SNV dbSNP153 33..33 33 - - - 109605 RMVar_ID_109605 Human_SNP_ID_72686190 m1A Human chr2 + 54664503 54664503 54664503 ACAAGCGAAATGGTCAACGGCGCTACAGAACAAAGGACGAGCTCTAAAGAGTCCAGCCCCATCCC ACAAGCGAAATGGTCAACGGCGCTACAGAACACAGGACGAGCTCTAAAGAGTCCAGCCCCATCCC A C SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:54664395..54664602 26863196 MeRIP-seq:(Medium) rs1558484429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57205,Human_RBP_ID_1196395,Human_RBP_ID_1919623,Human_RBP_ID_3628678,Human_RBP_ID_5589460,Human_RBP_ID_17699276,Human_RBP_ID_22393794,Human_RBP_ID_22993673,Human_RBP_ID_26488464,Human_RBP_ID_27012711 Human_Splice_Rec_245810,Human_Splice_Rec_245876 Human_miRNA_ID_2541162,Human_miRNA_ID_2544908,Human_miRNA_ID_2588184 RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_77244,RMVar_hsa_circ_199919,RMVar_hsa_circ_80058,RMVar_hsa_circ_199921,RMVar_hsa_circ_46316 109606 RMVar_ID_109606 Human_SNP_ID_72686191 m1A Human chr2 + 54664507 54664507 54664507 GCGAAATGGTCAACGGCGCTACAGAACAAAGGACGAGCTCTAAAGAGTCCAGCCCCATCCCCTCC GCGAAATGGTCAACGGCGCTACAGAACAAAGGGCGAGCTCTAAAGAGTCCAGCCCCATCCCCTCC A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:54664404..54664680;chr2:54664416..54664578 26863196 MeRIP-seq:(Medium) rs1292171873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57205,Human_RBP_ID_1919623,Human_RBP_ID_3628678,Human_RBP_ID_22393795,Human_RBP_ID_22993673,Human_RBP_ID_26488464 Human_Splice_Rec_245810,Human_Splice_Rec_245876 Human_miRNA_ID_2541162,Human_miRNA_ID_2543054,Human_miRNA_ID_2544908,Human_miRNA_ID_2546753,Human_miRNA_ID_2548621,Human_miRNA_ID_2550485,Human_miRNA_ID_2555887,Human_miRNA_ID_2557769,Human_miRNA_ID_2588184 RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_77244,RMVar_hsa_circ_199919,RMVar_hsa_circ_80058,RMVar_hsa_circ_199921,RMVar_hsa_circ_46316 109607 RMVar_ID_109607 Human_SNP_ID_72687343 m1A Human chr2 - 54668401 54668401 54668401 GTGCTCTGGGTGCTGGCAGACACCTCGTGTTTATCAGAGGAGATGGCGGAAGAGATAGCCTGGAT GTGCTCTGGGTGCTGGCAGACACCTCGTGTTTGTCAGAGGAGATGGCGGAAGAGATAGCCTGGAT T C AC093110.1 Ensembl:ENSG00000238018 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:54668351..54668425 26863196 MeRIP-seq:(Medium) rs993843828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199930 109608 RMVar_ID_109608 Human_SNP_ID_72687344 m1A Human chr2 - 54668401 54668401 54668401 GTGCTCTGGGTGCTGGCAGACACCTCGTGTTTATCAGAGGAGATGGCGGAAGAGATAGCCTGGAT GTGCTCTGGGTGCTGGCAGACACCTCGTGTTTCTCAGAGGAGATGGCGGAAGAGATAGCCTGGAT T G AC093110.1 Ensembl:ENSG00000238018 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:54668351..54668425 26863196 MeRIP-seq:(Medium) rs993843828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199930 109609 RMVar_ID_109609 Human_SNP_ID_72687794 m1A Human chr2 - 54669584 54669584 54669584 GGTACAGGTCGTACGACTGAGCACCAGGCCTGAGCGACCACCTCCCTGTTCAGGCCCAGCCTCTG GGTACAGGTCGTACGACTGAGCACCAGGCCTGGGCGACCACCTCCCTGTTCAGGCCCAGCCTCTG T C AC093110.1 Ensembl:ENSG00000238018 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:54669499..54669600 32194978 MeRIP-seq:(Medium) rs1425468254 Functional Loss SNV dbSNP153 33..33 33 - - - 109610 RMVar_ID_109610 Human_SNP_ID_72703250 m1A Human chr2 + 54723714 54723714 54723714 GGTGCGGGAGGCGGGGAGGGGAGGGCAGGCAGAGGATTTCGCTCGCTCGCCCGCGCGGGATCCGG GGTGCGGGAGGCGGGGAGGGGAGGGCAGGCAGGGGATTTCGCTCGCTCGCCCGCGCGGGATCCGG A G EML6 Ensembl:ENSG00000214595 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:54723664..54723777 26863196 MeRIP-seq:(Medium) rs1483361632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9428654,Human_RBP_ID_18421771,Human_RBP_ID_19001644 Human_Splice_Rec_245997,Human_Splice_Rec_246079,Human_Splice_Rec_246159 109611 RMVar_ID_109611 Human_SNP_ID_72786705 m1A Human chr2 + 54973052 54973052 54973052 GCTAAAAATAAAGATCTAACAACGATCTGTGAAACTGCACTGCAACGTCAAGGTTCGTTCTTCCC GCTAAAAATAAAGATCTAACAACGATCTGTGAGACTGCACTGCAACGTCAAGGTTCGTTCTTCCC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:54973001..54973186 32194978 MeRIP-seq:(Medium) rs202045881 Functional Loss SNV dbSNP153 33..33 33 - - - 109612 RMVar_ID_109612 Human_SNP_ID_72791043 m1A Human chr2 + 54987632 54987632 54987632 TCACAATGCTGAATACTGTCAATGAAAGCAGCAGGAATAGGCTGGCACCAAACACCACTCCAGTC TCACAATGCTGAATACTGTCAATGAAAGCAGCGGGAATAGGCTGGCACCAAACACCACTCCAGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:54987583..54987729 26863196 MeRIP-seq:(Medium) rs1276596623 Functional Loss SNV dbSNP153 33..33 33 - - - 109613 RMVar_ID_109613 Human_SNP_ID_72796938 m1A Human chr2 + 55010149 55010149 55010149 CCATCTCTTGTCACGATCTGCTTTGCAGCTCCAATTATTAATTATGCATACCAACAGAAAAGCTG CCATCTCTTGTCACGATCTGCTTTGCAGCTCCTATTATTAATTATGCATACCAACAGAAAAGCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:55010146..55010215 26863196 MeRIP-seq:(Medium) rs751949201 Functional Loss SNV dbSNP153 33..33 33 - - - 109614 RMVar_ID_109614 Human_SNP_ID_72800266 m1A Human chr2 + 55022896 55022896 55022896 GCTATTCCTCTGAAATTCTAAATTCAACATCCAACACACACACACACACACACACACACACACAC GCTATTCCTCTGAAATTCTAAATTCAACATCCCACACACACACACACACACACACACACACACAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:55022894..55023186;chr2:55022893..55023144 26863196 MeRIP-seq:(Medium) rs1440589943 Functional Loss SNV dbSNP153 33..33 33 - - - 109615 RMVar_ID_109615 Human_SNP_ID_72800454 m1A Human chr2 - 55023493 55023493 55023493 GAGCTTTGATTGTAGTGAGTGGAAAGGAAAGTATGGGGTATTGATACTGTTAGGGTTTTGTGACT GAGCTTTGATTGTAGTGAGTGGAAAGGAAAGTGTGGGGTATTGATACTGTTAGGGTTTTGTGACT T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55023491..55023601 26863196 MeRIP-seq:(Medium) rs1424018618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199954,RMVar_hsa_circ_285250,RMVar_hsa_circ_378931,RMVar_hsa_circ_199955,RMVar_hsa_circ_322485,RMVar_hsa_circ_199960 109616 RMVar_ID_109616 Human_SNP_ID_72808013 m1A Human chr2 + 55049980 55049980 55049980 GGCACGGTCGACGACACCGGGCTCGGGTCCCAAGACGGCTGCCGCTCCGGGGCGACGGGGGGAGC GGCACGGTCGACGACACCGGGCTCGGGTCCCACGACGGCTGCCGCTCCGGGGCGACGGGGGGAGC A C NONHSAG027791.2 RNACentral:URS00008C3286 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:55049174..55050487 32194978 MeRIP-seq:(Medium) rs1389721146 Functional Loss SNV dbSNP153 33..33 33 - - - 109617 RMVar_ID_109617 Human_SNP_ID_72808191 m1A Human chr2 + 55050290 55050290 55050290 TGTCCGAGGACGAGACCAGAGGAGACTGGTCCAGGTCTTCCATGGCTGGAGGGTGGAGATGATGC TGTCCGAGGACGAGACCAGAGGAGACTGGTCCTGGTCTTCCATGGCTGGAGGGTGGAGATGATGC A T NONHSAG027791.2 RNACentral:URS00008C3286 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:55049751..55050525 26863196 MeRIP-seq:(Medium) rs1449550475 Functional Loss SNV dbSNP153 33..33 33 - - - 109618 RMVar_ID_109618 Human_SNP_ID_72808231 m1A Human chr2 - 55050354 55050354 55050354 CCCCAACCCCCACAACCGCCCGCGGCTCTGAGACGCGGCCCCGGCGGCGGCGGCAGCAGCTGCAG CCCCAACCCCCACAACCGCCCGCGGCTCTGAGGCGCGGCCCCGGCGGCGGCGGCAGCAGCTGCAG T C RTN4 Ensembl:ENSG00000115310 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:55049751..55050500 26863196 MeRIP-seq:(Medium) rs1378293711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_145955,Human_RBP_ID_777707,Human_RBP_ID_9330468,Human_RBP_ID_17085259,Human_RBP_ID_17392654,Human_RBP_ID_22450332,Human_RBP_ID_22533532 109619 RMVar_ID_109619 Human_SNP_ID_72856143 m1A Human chr2 + 55227995 55227995 55227995 TCCCTGCAGACCATCCTCCTATATTACCCCCAACCCCCAAAACACATACATACTATCACTTTGAT TCCCTGCAGACCATCCTCCTATATTACCCCCAGCCCCCAAAACACATACATACTATCACTTTGAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:55227945..55228114 26863196 MeRIP-seq:(Medium) rs183761864 Functional Loss SNV dbSNP153 33..33 33 - - - 109620 RMVar_ID_109620 Human_SNP_ID_72857506 m1A Human chr2 - 55232710 55232710 55232710 CTAACCCGAGAGCAGCCGAAGTGCAGACACCCACCGCAGATGGCGGATCGAAAAGGAAGAACGCC CTAACCCGAGAGCAGCCGAAGTGCAGACACCCTCCGCAGATGGCGGATCGAAAAGGAAGAACGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:55232676..55232875;chr2:55232676..55232750 26863196 MeRIP-seq:(Medium) rs573092663 Functional Loss SNV dbSNP153 33..33 33 - - - 109621 RMVar_ID_109621 Human_SNP_ID_72857507 m1A Human chr2 - 55232710 55232710 55232710 CTAACCCGAGAGCAGCCGAAGTGCAGACACCCACCGCAGATGGCGGATCGAAAAGGAAGAACGCC CTAACCCGAGAGCAGCCGAAGTGCAGACACCCGCCGCAGATGGCGGATCGAAAAGGAAGAACGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:55232676..55232875;chr2:55232676..55232750 26863196 MeRIP-seq:(Medium) rs573092663 Functional Loss SNV dbSNP153 33..33 33 - - - 109622 RMVar_ID_109622 Human_SNP_ID_72857577 m1A Human chr2 + 55232819 55232819 55232819 CTTCCTTTTCCTCAACCTCAGGTGGAGCCGCCACCAAAATGCAGATTTTCGTGAAAACCCTTACG CTTCCTTTTCCTCAACCTCAGGTGGAGCCGCCCCCAAAATGCAGATTTTCGTGAAAACCCTTACG A C RPS27A Ensembl:ENSG00000143947 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55232676..55232875 26863196 MeRIP-seq:(Medium) rs754706035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242906,Human_RBP_ID_552454,Human_RBP_ID_775998,Human_RBP_ID_4623310,Human_RBP_ID_17657436,Human_RBP_ID_22451279,Human_RBP_ID_22533534,Human_RBP_ID_23876921,Human_RBP_ID_26818465 Human_Splice_Rec_246592,Human_Splice_Rec_246593,Human_Splice_Rec_246600,Human_Splice_Rec_246601,Human_Splice_Rec_246608,Human_Splice_Rec_246609,Human_Splice_Rec_246612,Human_Splice_Rec_246613,Human_Splice_Rec_246617,Human_Splice_Rec_246624,Human_Splice_Rec_246626,Human_Splice_Rec_246627,Human_Splice_Rec_246630,Human_Splice_Rec_246631,Human_Splice_Rec_246635,Human_Splice_Rec_246637 Human_miRNA_ID_980270,Human_miRNA_ID_984999 RMVar_hsa_circ_199981,RMVar_hsa_circ_122622,RMVar_hsa_circ_315327,RMVar_hsa_circ_369810,RMVar_hsa_circ_199983,RMVar_hsa_circ_77479,RMVar_hsa_circ_199982,RMVar_hsa_circ_199980 109623 RMVar_ID_109623 Human_SNP_ID_72858641 m1A Human chr2 - 55235508 55235508 55235508 CAACATTTGCCACAATAATGTCTGTCAAAGTGACTTGCCATAAACACCCCAGCACCACATTCATC CAACATTTGCCACAATAATGTCTGTCAAAGTGGCTTGCCATAAACACCCCAGCACCACATTCATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55235399..55235546 26863196 MeRIP-seq:(Medium) rs973413098 Functional Loss SNV dbSNP153 33..33 33 - - - 109624 RMVar_ID_109624 Human_SNP_ID_72861197 m1A Human chr2 - 55243561 55243561 55243561 ATAGAAGAAAAGCGAAAGGAACACAAAGAAGCACATCAGAAAGCCCGTGAGAAGTATGGCCATCT ATAGAAGAAAAGCGAAAGGAACACAAAGAAGCGCATCAGAAAGCCCGTGAGAAGTATGGCCATCT T C MTIF2 Ensembl:ENSG00000085760 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55243511..55243647 26863196 MeRIP-seq:(Medium) rs770848031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920335,Human_RBP_ID_26340907 Human_miRNA_ID_2235968 RMVar_hsa_circ_22221,RMVar_hsa_circ_56902,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_364367,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_31315,RMVar_hsa_circ_304864,RMVar_hsa_circ_354196 109625 RMVar_ID_109625 Human_SNP_ID_72861205 m1A Human chr2 - 55243583 55243583 55243583 AGGTCAGGAGGATCTGAAAATAATAGAAGAAAAGCGAAAGGAACACAAAGAAGCACATCAGAAAG AGGTCAGGAGGATCTGAAAATAATAGAAGAAAGGCGAAAGGAACACAAAGAAGCACATCAGAAAG T C MTIF2 Ensembl:ENSG00000085760 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55243486..55243650 26863196 MeRIP-seq:(Medium) rs1244529776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920335,Human_RBP_ID_2652005,Human_RBP_ID_26340907 Human_Splice_Rec_246664,Human_Splice_Rec_246692,Human_Splice_Rec_246716,Human_Splice_Rec_246730 RMVar_hsa_circ_22221,RMVar_hsa_circ_56902,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_364367,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_31315,RMVar_hsa_circ_304864,RMVar_hsa_circ_354196 109626 RMVar_ID_109626 Human_SNP_ID_72861206 m1A Human chr2 - 55243586 55243586 55243586 GAAAGGTCAGGAGGATCTGAAAATAATAGAAGAAAAGCGAAAGGAACACAAAGAAGCACATCAGA GAAAGGTCAGGAGGATCTGAAAATAATAGAAGGAAAGCGAAAGGAACACAAAGAAGCACATCAGA T C MTIF2 Ensembl:ENSG00000085760 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:55243536..55243636 26863196 MeRIP-seq:(Medium) rs764176987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_920335,Human_RBP_ID_2652005,Human_RBP_ID_6931559,Human_RBP_ID_17699999,Human_RBP_ID_26340907 Human_Splice_Rec_246664,Human_Splice_Rec_246692,Human_Splice_Rec_246716,Human_Splice_Rec_246730 RMVar_hsa_circ_22221,RMVar_hsa_circ_56902,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_364367,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_31315,RMVar_hsa_circ_304864,RMVar_hsa_circ_354196 109627 RMVar_ID_109627 Human_SNP_ID_72868775 m1A Human chr2 - 55269484 55269483 55269484 AGGAAAGAAAGGAGAGGGACAGAAAGAAAAAAAGGAAAGAGAGAAAGAAAGGAAAGGAAAGTAAG AGGAAAGAAAGGAGAGGGACAGAAAGAAAAAA_GGAAAGAGAGAAAGAAAGGAAAGGAAAGTAAG CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55269438..55269527 26863196 MeRIP-seq:(Medium) rs1360918943 Functional Loss DEL dbSNP153 33..33 33 - - - 109628 RMVar_ID_109628 Human_SNP_ID_72896638 m1A Human chr2 + 55373282 55373282 55373282 TACTTTCTAGCTATGCTGAGCCATTAATCACCATTCTTCCCAAATATGCATATATACAACTCCTC TACTTTCTAGCTATGCTGAGCCATTAATCACCGTTCTTCCCAAATATGCATATATACAACTCCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55373234..55373318 26863196 MeRIP-seq:(Medium) rs956503152 Functional Loss SNV dbSNP153 33..33 33 - - - 109629 RMVar_ID_109629 Human_SNP_ID_72910917 m1A Human chr2 + 55419791 55419791 55419791 AGCCCTGCCAGCCTTTCAGCGCGTCTCTGGGAATCCCTGGCACAAAATCACCGCCGCGCTCCAGC AGCCCTGCCAGCCTTTCAGCGCGTCTCTGGGATTCCCTGGCACAAAATCACCGCCGCGCTCCAGC A T lnc-CFAP36-5 RNACentral:URS00008B7F27 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55419570..55419871 26863196 MeRIP-seq:(Medium) rs557547038 Functional Loss SNV dbSNP153 33..33 33 - - - 109630 RMVar_ID_109630 Human_SNP_ID_72940380 m1A Human chr2 - 55519732 55519732 55519732 AGACCGCCGGACCCCGGTTAGGCCTTTGGGCCACAAGGAGCCGAGAGGGAGTAGGGGAAGAGCTG AGACCGCCGGACCCCGGTTAGGCCTTTGGGCCGCAAGGAGCCGAGAGGGAGTAGGGGAAGAGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55519685..55519859 26863196 MeRIP-seq:(Medium) rs1432751667 Functional Loss SNV dbSNP153 33..33 33 - - - 109631 RMVar_ID_109631 Human_SNP_ID_72940381 m1A Human chr2 - 55519732 55519732 55519732 AGACCGCCGGACCCCGGTTAGGCCTTTGGGCCACAAGGAGCCGAGAGGGAGTAGGGGAAGAGCTG AGACCGCCGGACCCCGGTTAGGCCTTTGGGCCCCAAGGAGCCGAGAGGGAGTAGGGGAAGAGCTG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55519685..55519859 26863196 MeRIP-seq:(Medium) rs1432751667 Functional Loss SNV dbSNP153 33..33 33 - - - 109632 RMVar_ID_109632 Human_SNP_ID_72940403 m1A Human chr2 - 55519777 55519777 55519777 GCAGCCATCCCGCCCCAAAGGGGCAACGGGGAAGATCCCTAGGCCAGACCGCCGGACCCCGGTTA GCAGCCATCCCGCCCCAAAGGGGCAACGGGGAGGATCCCTAGGCCAGACCGCCGGACCCCGGTTA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:55519726..55519825 32194978 MeRIP-seq:(Medium) rs751770746 Functional Loss SNV dbSNP153 33..33 33 - - - 109633 RMVar_ID_109633 Human_SNP_ID_72940436 m1A Human chr2 + 55519837 55519837 55519837 GCTGCGGAAGAAGAAGACGAGGTGGAGTGGGTAGTGGAGAGCATCGCGGGGTTCCTGCGAGGCCC GCTGCGGAAGAAGAAGACGAGGTGGAGTGGGTGGTGGAGAGCATCGCGGGGTTCCTGCGAGGCCC A G CFAP36 Ensembl:ENSG00000163001 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:55519739..55519854 26863196 MeRIP-seq:(Medium) rs774453282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4623321,Human_RBP_ID_5471406,Human_RBP_ID_26339341 Human_Splice_Rec_248577,Human_Splice_Rec_248597,Human_Splice_Rec_248611,Human_Splice_Rec_248629,Human_Splice_Rec_248647 109634 RMVar_ID_109634 Human_SNP_ID_72947035 m1A Human chr2 + 55544332 55544332 55544332 GAGAAAGGATATGAGGACTAAACAGATACAAAATATGGAGCAGAAAGGAAAACCCACTGGGGAGG GAGAAAGGATATGAGGACTAAACAGATACAAAGTATGGAGCAGAAAGGAAAACCCACTGGGGAGG A G CFAP36 Ensembl:ENSG00000163001 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55544281..55544399 26863196 MeRIP-seq:(Medium) rs779350603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1920017,Human_RBP_ID_17657581,Human_RBP_ID_22595363,Human_RBP_ID_26339346,Human_RBP_ID_27817135 Human_Splice_Rec_248595,Human_Splice_Rec_248627,Human_Splice_Rec_248645,Human_Splice_Rec_248667 109635 RMVar_ID_109635 Human_SNP_ID_72947050 m1A Human chr2 - 55544365 55544365 55544365 AATCTTGACATATTAAGGCTAGCCATACCTCTACCTCCCCAGTGGGTTTTCCTTTCTGCTCCATA AATCTTGACATATTAAGGCTAGCCATACCTCTGCCTCCCCAGTGGGTTTTCCTTTCTGCTCCATA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55544315..55544399 26863196 MeRIP-seq:(Medium) rs1196311266 Functional Loss SNV dbSNP153 33..33 33 - - - 109636 RMVar_ID_109636 Human_SNP_ID_73045956 m1A Human chr2 + 55881718 55881718 55881718 ACTTGGTCTGCTCTACAGTTGTGCGTCCCTGCAGTGCACTCGTCTATGTCTGTCAGAGACATGCA ACTTGGTCTGCTCTACAGTTGTGCGTCCCTGCGGTGCACTCGTCTATGTCTGTCAGAGACATGCA A G lnc-CCDC85A-4 RNACentral:URS00008B9ADD lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55881567..55881786 26863196 MeRIP-seq:(Medium) rs776323409 Functional Loss SNV dbSNP153 33..33 33 - - - 109637 RMVar_ID_109637 Human_SNP_ID_73054228 m1A Human chr2 - 55917753 55917753 55917753 GGCCGAAATAACTTTGTCATCCGGCGGAACCCAGCTGACCCTCAGCGCATTCCCTCCAACCCTTC GGCCGAAATAACTTTGTCATCCGGCGGAACCCGGCTGACCCTCAGCGCATTCCCTCCAACCCTTC T C EFEMP1 Ensembl:ENSG00000115380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55917646..55917871 26863196 MeRIP-seq:(Medium) rs368195380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57326 Human_Splice_Rec_248965,Human_Splice_Rec_248985,Human_Splice_Rec_249005,Human_Splice_Rec_249015 RMVar_hsa_circ_93810,RMVar_hsa_circ_342235,RMVar_hsa_circ_335325,RMVar_hsa_circ_200114,RMVar_hsa_circ_200115,RMVar_hsa_circ_200113,RMVar_hsa_circ_104113,RMVar_hsa_circ_105620,RMVar_hsa_circ_200116,RMVar_hsa_circ_115793,RMVar_hsa_circ_200117,RMVar_hsa_circ_200118,RMVar_hsa_circ_112801,RMVar_hsa_circ_85349,RMVar_hsa_circ_101559,RMVar_hsa_circ_117377,RMVar_hsa_circ_200121,RMVar_hsa_circ_88174,RMVar_hsa_circ_200122,RMVar_hsa_circ_200124,RMVar_hsa_circ_200125,RMVar_hsa_circ_200123 109638 RMVar_ID_109638 Human_SNP_ID_73055321 m1A Human chr2 - 55922410 55922410 55922410 CAATGTTGAAAGCCCTTTTCCTAACTATGCTGACTCTGGCGCTGGTCAAGTCACAGGACACCGAA CAATGTTGAAAGCCCTTTTCCTAACTATGCTGTCTCTGGCGCTGGTCAAGTCACAGGACACCGAA T A EFEMP1 Ensembl:ENSG00000115380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55922313..55922481 26863196 MeRIP-seq:(Medium) rs760892091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57337,Human_RBP_ID_2653284,Human_RBP_ID_8521820,Human_RBP_ID_27158633,Human_RBP_ID_27480772 Human_Splice_Rec_248960,Human_Splice_Rec_248961,Human_Splice_Rec_248980,Human_Splice_Rec_248981,Human_Splice_Rec_249000,Human_Splice_Rec_249001,Human_Splice_Rec_249028,Human_Splice_Rec_249029,Human_Splice_Rec_249034,Human_Splice_Rec_249035,Human_Splice_Rec_249044,Human_Splice_Rec_249045,Human_Splice_Rec_249054,Human_Splice_Rec_249055,Human_Splice_Rec_249064,Human_Splice_Rec_249065,Human_Splice_Rec_249073,Human_Splice_Rec_249079,Human_Splice_Rec_249084,Human_Splice_Rec_249090 Human_miRNA_ID_2375855 RMVar_hsa_circ_93810,RMVar_hsa_circ_200115,RMVar_hsa_circ_104113,RMVar_hsa_circ_200116,RMVar_hsa_circ_85349,RMVar_hsa_circ_101559,RMVar_hsa_circ_200124,RMVar_hsa_circ_200125 109639 RMVar_ID_109639 Human_SNP_ID_73055709 m1A Human chr2 + 55923759 55923759 55923759 CGCTCCGGGCCCGGGCAGCGAGGGGAGTGCGCAGGGGAGGGCAGCCCCGTGGGTCTGATCTGGCG CGCTCCGGGCCCGGGCAGCGAGGGGAGTGCGCGGGGGAGGGCAGCCCCGTGGGTCTGATCTGGCG A G lnc-CCDC85A-4 RNACentral:URS00008B9ADD lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:55923662..55923800;chr2:55923663..55923843;chr2:55923537..55923825 26863196 MeRIP-seq:(Medium) rs1263292601 Functional Loss SNV dbSNP153 33..33 33 - - - 109640 RMVar_ID_109640 Human_SNP_ID_73124668 m1A Human chr2 + 56184157 56184157 56184157 GCCGCGGTGCCCGGCGCGCCCTCCAAGCTAGGAGAGGGGAGAAGCCGGGGGCTGCAGCTGGGCAA GCCGCGGTGCCCGGCGCGCCCTCCAAGCTAGGGGAGGGGAGAAGCCGGGGGCTGCAGCTGGGCAA A G AC007744.1,CCDC85A Ensembl:ENSG00000271894,Ensembl:ENSG00000055813 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:56184107..56184200 26863196 MeRIP-seq:(Medium) rs1368081454 Functional Loss SNV dbSNP153 33..33 33 - - - 109641 RMVar_ID_109641 Human_SNP_ID_73178889 m1A Human chr2 + 56384346 56384346 56384346 AGGCAACATTTGTCAGGAAACCAGTACAAAGGACCAATGTGAGATGCACTCTTTTTCAAACAGGA AGGCAACATTTGTCAGGAAACCAGTACAAAGGGCCAATGTGAGATGCACTCTTTTTCAAACAGGA A G AC007744.1,CCDC85A Ensembl:ENSG00000271894,Ensembl:ENSG00000055813 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:56342920..56384380 32194978 MeRIP-seq:(Medium) rs778696528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_249116,Human_Splice_Rec_249152 RMVar_hsa_circ_266112 109642 RMVar_ID_109642 Human_SNP_ID_73662310 m1A Human chr2 + 58046759 58046759 58046759 AAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGAGTGCTGGGCCCGCCTCCCCGCGGGACTGTAGG AAGTTAGGCAGGTCCTAGGGAGGGCAGGCTCGGGTGCTGGGCCCGCCTCCCCGCGGGACTGTAGG A G VRK2 Ensembl:ENSG00000028116 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:58046716..58046959 26863196 MeRIP-seq:(Medium) rs1379004299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243366 Human_Splice_Rec_249331,Human_Splice_Rec_249357 109643 RMVar_ID_109643 Human_SNP_ID_73662992 m1A Human chr2 + 58048828 58048828 58048828 TACCCATTTATCTCACCCCTTCTGCCAACAGAAGTGATGCCACCAAAAAGAAATGAAAAATACAA TACCCATTTATCTCACCCCTTCTGCCAACAGAGGTGATGCCACCAAAAAGAAATGAAAAATACAA A G VRK2 Ensembl:ENSG00000028116 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:58048826..58048931 26863196 MeRIP-seq:(Medium) rs1330503365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827979,Human_RBP_ID_25574926 Human_Splice_Rec_249184,Human_Splice_Rec_249216,Human_Splice_Rec_249244,Human_Splice_Rec_249286,Human_Splice_Rec_249308,Human_Splice_Rec_249332,Human_Splice_Rec_249384 RMVar_hsa_circ_200133,RMVar_hsa_circ_353433,RMVar_hsa_circ_356263,RMVar_hsa_circ_282208 109644 RMVar_ID_109644 Human_SNP_ID_73715787 m1A Human chr2 + 58230965 58230965 58230965 TTTTTCTTCAAAATACTTTATACTTTCCTCCCACTCATCCAACACAAATGGCTTCTGCCACCACA TTTTTCTTCAAAATACTTTATACTTTCCTCCCGCTCATCCAACACAAATGGCTTCTGCCACCACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:58230960..58231177;chr2:58230961..58231100 26863196 MeRIP-seq:(Medium) rs1036373183 Functional Loss SNV dbSNP153 33..33 33 - - - 109645 RMVar_ID_109645 Human_SNP_ID_73718639 m1A Human chr2 + 58241289 58241289 58241289 GTTCTGGGGCAGAAGCAGGGGGCACTGGCGCAACAGGCTCGCTTCCGTCACCGCCATGGCTCGAA GTTCTGGGGCAGAAGCAGGGGGCACTGGCGCAGCAGGCTCGCTTCCGTCACCGCCATGGCTCGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:58241169..58241303 26863196 MeRIP-seq:(Medium) rs1239119148 Functional Loss SNV dbSNP153 33..33 33 - - - 109646 RMVar_ID_109646 Human_SNP_ID_73718652 m1A Human chr2 - 58241299 58241299 58241299 TTCTCCGGACTTCGAGCCATGGCGGTGACGGAAGCGAGCCTGTTGCGCCAGTGCCCCCTGCTTCT TTCTCCGGACTTCGAGCCATGGCGGTGACGGAGGCGAGCCTGTTGCGCCAGTGCCCCCTGCTTCT T C FANCL Ensembl:ENSG00000115392 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr2:58241201..58241350;chr2:58241170..58241353;chr2:58241189..58241313 26863196 MeRIP-seq:(Medium) rs1249154309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_552804,Human_RBP_ID_4623326,Human_RBP_ID_5589486,Human_RBP_ID_8521975,Human_RBP_ID_13923989,Human_RBP_ID_18421779,Human_RBP_ID_22076288,Human_RBP_ID_26340929 Human_Splice_Rec_249393,Human_Splice_Rec_249417,Human_Splice_Rec_249443,Human_Splice_Rec_249469,Human_Splice_Rec_249487,Human_Splice_Rec_249505,Human_Splice_Rec_249517,Human_Splice_Rec_249537,Human_Splice_Rec_249545 109647 RMVar_ID_109647 Human_SNP_ID_73721570 m1A Human chr2 + 58251976 58251976 58251976 CCAAATGAGCTCATCCTGGGCTGGTACGCTACAGGCCATGACATCACAGAGCACTCTGTGCTGAT CCAAATGAGCTCATCCTGGGCTGGTACGCTACCGGCCATGACATCACAGAGCACTCTGTGCTGAT A C EIF3FP3 Ensembl:ENSG00000233426 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112561538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258763,Human_RBP_ID_17280235,Human_RBP_ID_17510354 Human_miRNA_ID_1895685,Human_miRNA_ID_1904935 109648 RMVar_ID_109648 Human_SNP_ID_73721571 m1A Human chr2 + 58251976 58251976 58251976 CCAAATGAGCTCATCCTGGGCTGGTACGCTACAGGCCATGACATCACAGAGCACTCTGTGCTGAT CCAAATGAGCTCATCCTGGGCTGGTACGCTACGGGCCATGACATCACAGAGCACTCTGTGCTGAT A G EIF3FP3 Ensembl:ENSG00000233426 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112561538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8258763,Human_RBP_ID_17280235,Human_RBP_ID_17510354 Human_miRNA_ID_1895685,Human_miRNA_ID_1904935 109649 RMVar_ID_109649 Human_SNP_ID_252398854 m1A Human chr5 + 135027836 135027835 135027837 GTCAGTCCAACATACACAGGGACGCTGTAAACAGGGGCGCGGGCCGGAGAGCGGGTGTGCAAAGT GTCAGTCCAACATACACAGGGACGCTGTAAAC__GGGCGCGGGCCGGAGAGCGGGTGTGCAAAGT CAG C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:135027792..135027862 26863196 MeRIP-seq:(Medium) rs752270603 Functional Loss DEL dbSNP153 33..34 33 - - - 109650 RMVar_ID_109650 Human_SNP_ID_252398856 m1A Human chr5 + 135027836 135027836 135027836 GTCAGTCCAACATACACAGGGACGCTGTAAACAGGGGCGCGGGCCGGAGAGCGGGTGTGCAAAGT GTCAGTCCAACATACACAGGGACGCTGTAAACGGGGGCGCGGGCCGGAGAGCGGGTGTGCAAAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:135027792..135027862 26863196 MeRIP-seq:(Medium) rs1463424088 Functional Loss SNV dbSNP153 33..33 33 - - - 109651 RMVar_ID_109651 Human_SNP_ID_252399143 m1A Human chr5 - 135028517 135028517 135028517 GCAAAAAGACGTCGGAGAAAAGTGCCGCGAAAAAATGGATGAGTTGCAATTTCTCTCGGGATGGC GCAAAAAGACGTCGGAGAAAAGTGCCGCGAAAGAATGGATGAGTTGCAATTTCTCTCGGGATGGC T C PITX1 Ensembl:ENSG00000069011 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:135028314..135028547 26863196 MeRIP-seq:(Medium) rs1400289084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632041,Human_RBP_ID_2896042 RMVar_hsa_circ_234631,RMVar_hsa_circ_86064,RMVar_hsa_circ_121618,RMVar_hsa_circ_234632 109652 RMVar_ID_109652 Human_SNP_ID_252399452 m1A Human chr5 - 135029087 135029087 135029087 TCAACTCCATGAGCCCGCTGTCGTCGCAGTCCATGTTCTCAGCACCCAGCTCCATCTCCTCCATG TCAACTCCATGAGCCCGCTGTCGTCGCAGTCCGTGTTCTCAGCACCCAGCTCCATCTCCTCCATG T C PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr5:135028379..135029341;chr5:135028960..135029206 26863196 MeRIP-seq:(Medium) rs138042194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18195111,Human_RBP_ID_22295745,Human_RBP_ID_27331366,Human_RBP_ID_27511489 Human_miRNA_ID_1980298,Human_miRNA_ID_1982024 RMVar_hsa_circ_234631,RMVar_hsa_circ_86064,RMVar_hsa_circ_121618,RMVar_hsa_circ_234632 109653 RMVar_ID_109653 Human_SNP_ID_252400088 m1A Human chr5 - 135031329 135031329 135031329 CCACGTTCCAGAGGAACCGCTACCCCGACATGAGCATGAGGGAGGAGATCGCCGTGTGGACCAAC CCACGTTCCAGAGGAACCGCTACCCCGACATGGGCATGAGGGAGGAGATCGCCGTGTGGACCAAC T C PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:135031233..135031501 26863196 MeRIP-seq:(Medium) rs1262985450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632044,Human_RBP_ID_838617,Human_RBP_ID_946340,Human_RBP_ID_18195113,Human_RBP_ID_22100181,Human_RBP_ID_26826542 Human_Splice_Rec_693661,Human_Splice_Rec_693667,Human_Splice_Rec_693671,Human_Splice_Rec_693673 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109654 RMVar_ID_109654 Human_SNP_ID_252400099 m1A Human chr5 - 135031366 135031366 135031366 ACGCACTTCACAAGCCAGCAGTTGCAAGAGCTAGAGGCCACGTTCCAGAGGAACCGCTACCCCGA ACGCACTTCACAAGCCAGCAGTTGCAAGAGCTGGAGGCCACGTTCCAGAGGAACCGCTACCCCGA T C PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:135031177..135031525 26863196 MeRIP-seq:(Medium) rs1220641579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_693661,Human_Splice_Rec_693667,Human_Splice_Rec_693671,Human_Splice_Rec_693673 Human_miRNA_ID_1968312 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109655 RMVar_ID_109655 Human_SNP_ID_252400106 m1A Human chr5 - 135031389 135031389 135031389 AGAAGAAGCAGCGGCGGCAACGTACGCACTTCACAAGCCAGCAGTTGCAAGAGCTAGAGGCCACG AGAAGAAGCAGCGGCGGCAACGTACGCACTTCGCAAGCCAGCAGTTGCAAGAGCTAGAGGCCACG T C PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:135031339..135031563 26863196 MeRIP-seq:(Medium) rs1375931542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2472360 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109656 RMVar_ID_109656 Human_SNP_ID_252400614 m1A Human chr5 + 135033080 135033080 135033080 GAGGGAGACGCGCAGGAGCCGGGGCGGGGGCCAGAGCCGGGCTGCTCCGGGCTTCGGCCGCGCAC GAGGGAGACGCGCAGGAGCCGGGGCGGGGGCCGGAGCCGGGCTGCTCCGGGCTTCGGCCGCGCAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:135033072..135033161 26863196 MeRIP-seq:(Medium) rs1432306209 Functional Loss SNV dbSNP153 33..33 33 - - - 109657 RMVar_ID_109657 Human_SNP_ID_252400701 m1A Human chr5 - 135033273 135033273 135033273 AGGTTAACACCGTGACAGTAGGCGACAGAATGAAAGAGACCAAAGAGAAGGGGCGGGCGGGAAGG AGGTTAACACCGTGACAGTAGGCGACAGAATGGAAGAGACCAAAGAGAAGGGGCGGGCGGGAAGG T C PITX1 Ensembl:ENSG00000069011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:135033251..135033480 26863196 MeRIP-seq:(Medium) rs1349552876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5610322,Human_RBP_ID_8236724 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109658 RMVar_ID_109658 Human_SNP_ID_252400706 m1A Human chr5 - 135033286 135033284 135033287 GAGACAGAGAGGGAGGTTAACACCGTGACAGTAGGCGACAGAATGAAAGAGACCAAAGAGAAGGG GAGACAGAGAGGGAGGTTAACACCGTGACAG___GCGACAGAATGAAAGAGACCAAAGAGAAGGG CCTA C PITX1 Ensembl:ENSG00000069011 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:135033276..135033480;chr5:135033251..135052493 26863196 MeRIP-seq:(Medium) rs1473185060 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5610322,Human_RBP_ID_8236724 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109659 RMVar_ID_109659 Human_SNP_ID_252400871 m1A Human chr5 - 135033769 135033769 135033769 GGGGCCCGCCTTCCACCTGGCCCGGCCCGCCGACCCCCGCGAGCCGCTCGAGAACTCCGCCAGCG GGGGCCCGCCTTCCACCTGGCCCGGCCCGCCGCCCCCCGCGAGCCGCTCGAGAACTCCGCCAGCG T G PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:135033726..135033995 26863196 MeRIP-seq:(Medium) rs1044912477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24083974,Human_RBP_ID_26826543 Human_Splice_Rec_693659,Human_Splice_Rec_693665,Human_Splice_Rec_693677,Human_Splice_Rec_693681 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109660 RMVar_ID_109660 Human_SNP_ID_252400872 m1A Human chr5 + 135033791 135033770 135033791 CTCGCGGGGGTCGGCGGGCCGGGCCAGGTGGAAGGCGGGCCCCATGTCATGGGGTGGCGGCGGCG CTCGCGGGGGTC_____________________GGCGGGCCCCATGTCATGGGGTGGCGGCGGCG CGGCGGGCCGGGCCAGGTGGAA C C5orf66 Ensembl:ENSG00000224186 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:135033680..135034025;chr5:135033690..135034239 26863196 MeRIP-seq:(Medium) rs770618968 Functional Loss DEL dbSNP153 13..33 33 - - - RMVar_hsa_circ_234633,RMVar_hsa_circ_106139 109661 RMVar_ID_109661 Human_SNP_ID_252400889 m1A Human chr5 - 135033808 135033808 135033808 GGAGGGGCTCCGGCCGCCGCCGCCGCCACCCCATGACATGGGGCCCGCCTTCCACCTGGCCCGGC GGAGGGGCTCCGGCCGCCGCCGCCGCCACCCCCTGACATGGGGCCCGCCTTCCACCTGGCCCGGC T G PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:135033769..135034017 32194978 MeRIP-seq:(Medium) rs758332384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5242422,Human_RBP_ID_5426858 Human_Splice_Rec_693659,Human_Splice_Rec_693665,Human_Splice_Rec_693677,Human_Splice_Rec_693681 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109662 RMVar_ID_109662 Human_SNP_ID_252400986 m1A Human chr5 - 135034044 135034044 135034044 AGCTGCCGCCGCCTCTGCCCGCCCGGCGCCGCAGCCCCGGGCGGTCCATGGGGCGGGCACGGCGT AGCTGCCGCCGCCTCTGCCCGCCCGGCGCCGCGGCCCCGGGCGGTCCATGGGGCGGGCACGGCGT T C PITX1 Ensembl:ENSG00000069011 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:135033966..135034116 26863410 MeRIP-seq:(Medium) rs1324313058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4809912 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109663 RMVar_ID_109663 Human_SNP_ID_252401029 m1A Human chr5 - 135034156 135034156 135034156 GGCCCCGGATCGCGAGCCGGAGCCGGAGCCGGAGCCGGGGCCGGCCGGGCTGCTGAGGCCCGAGC GGCCCCGGATCGCGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGCCGGGCTGCTGAGGCCCGAGC T C PITX1 Ensembl:ENSG00000069011 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:135034065..135034165 26863410 MeRIP-seq:(Medium) rs878943658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845366,Human_RBP_ID_5326545,Human_RBP_ID_8894089,Human_RBP_ID_9306603 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 109664 RMVar_ID_109664 Human_SNP_ID_252413737 m1A Human chr5 + 135086949 135086949 135086949 ATGCTAAAGGAGAGGGAGGAGGAGGGGCTTGCATGAGGGCAGAGCCACTCCAGAGTTGGAGGTGC ATGCTAAAGGAGAGGGAGGAGGAGGGGCTTGCGTGAGGGCAGAGCCACTCCAGAGTTGGAGGTGC A G C5orf66 Ensembl:ENSG00000224186 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:135086858..135086948 26863196 MeRIP-seq:(Medium) rs942241815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234633,RMVar_hsa_circ_106139,RMVar_hsa_circ_373829,RMVar_hsa_circ_272628,RMVar_hsa_circ_234635,RMVar_hsa_circ_338893 109665 RMVar_ID_109665 Human_SNP_ID_252431556 m1A Human chr5 + 135164302 135164302 135164302 TAAGTGGATGATGTAGTATGCTAGAATGTAAGAAAGGCTACAGAAAACAGCAGGCCTAGAGGTTT TAAGTGGATGATGTAGTATGCTAGAATGTAAGGAAGGCTACAGAAAACAGCAGGCCTAGAGGTTT A G C5orf66 Ensembl:ENSG00000224186 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:135164237..135164320 26863196 MeRIP-seq:(Medium) rs892009219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234633,RMVar_hsa_circ_106139,RMVar_hsa_circ_373829,RMVar_hsa_circ_272628,RMVar_hsa_circ_234635,RMVar_hsa_circ_338893 109666 RMVar_ID_109666 Human_SNP_ID_252470229 m1A Human chr5 + 135334577 135334577 135334577 GAGGGGGGAAACCAAAAGAACATTAGAGTAAAAAGAACGCCACTGGAGGATGTACAATAAAGCAC GAGGGGGGAAACCAAAAGAACATTAGAGTAAATAGAACGCCACTGGAGGATGTACAATAAAGCAC A T C5orf66 Ensembl:ENSG00000224186 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:135334526..135334625 32194978 MeRIP-seq:(Medium) rs892343208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373829,RMVar_hsa_circ_234635 109667 RMVar_ID_109667 Human_SNP_ID_252470241 m1A Human chr5 - 135334622 135334622 135334622 CCTGTCACCGAAGCCAGGAAGCCCCGTTTGTAAGCGTGTGTTGTGGTGCTTTATTGTACATCCTC CCTGTCACCGAAGCCAGGAAGCCCCGTTTGTATGCGTGTGTTGTGGTGCTTTATTGTACATCCTC T A MACROH2A1 Ensembl:ENSG00000113648 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:135334571..135334688 26863196 MeRIP-seq:(Medium) rs754062253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632054,Human_RBP_ID_1109836,Human_RBP_ID_1987187,Human_RBP_ID_3758198,Human_RBP_ID_9169780,Human_RBP_ID_23050952,Human_RBP_ID_23214518,Human_RBP_ID_24084015,Human_RBP_ID_24509082,Human_RBP_ID_26530517,Human_RBP_ID_26827401 109668 RMVar_ID_109668 Human_SNP_ID_252474912 m1A Human chr5 - 135354608 135354608 135354608 CTCTGTCCTGGTGCCAGGGCTCTGAGCTGCTGAGAGCTTCGCTTTGTGAGATCACCCCCATGGCT CTCTGTCCTGGTGCCAGGGCTCTGAGCTGCTGGGAGCTTCGCTTTGTGAGATCACCCCCATGGCT T C MACROH2A1 Ensembl:ENSG00000113648 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:135354606..135354700 26863196 MeRIP-seq:(Medium) rs935663028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1108238,Human_RBP_ID_1987218,Human_RBP_ID_10182415,Human_RBP_ID_24084041,Human_RBP_ID_25857567 RMVar_hsa_circ_29887,RMVar_hsa_circ_283499,RMVar_hsa_circ_48904,RMVar_hsa_circ_287214,RMVar_hsa_circ_234638,RMVar_hsa_circ_60451 109669 RMVar_ID_109669 Human_SNP_ID_252476090 m1A Human chr5 + 135360250 135360250 135360250 CTCCAGACTAACCAAGGGTCCCCATCTCCCACAGGAGCTGCCTGCCCTCTTCTTTTTTACCACTG CTCCAGACTAACCAAGGGTCCCCATCTCCCACTGGAGCTGCCTGCCCTCTTCTTTTTTACCACTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:135360247..135360410 26863196 MeRIP-seq:(Medium) rs531753071 Functional Loss SNV dbSNP153 33..33 33 - - - 109670 RMVar_ID_109670 Human_SNP_ID_252476193 m1A Human chr5 - 135360577 135360577 135360577 AGAAGAAGCAGGGTGAAGTCAGTAAGGCAGCCAGCGCCGACAGCACAACCGAGGGCACACCTGCC AGAAGAAGCAGGGTGAAGTCAGTAAGGCAGCCGGCGCCGACAGCACAACCGAGGGCACACCTGCC T C MACROH2A1 Ensembl:ENSG00000113648 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:135360526..135360642;chr5:135360526..135360652 26863196 MeRIP-seq:(Medium) rs1171135651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632084,Human_RBP_ID_9398196,Human_RBP_ID_22680708,Human_RBP_ID_22827175 Human_Splice_Rec_693744,Human_Splice_Rec_693745,Human_Splice_Rec_693772,Human_Splice_Rec_693773,Human_Splice_Rec_693788,Human_Splice_Rec_693789,Human_Splice_Rec_693804,Human_Splice_Rec_693805,Human_Splice_Rec_693823,Human_Splice_Rec_693844,Human_Splice_Rec_693845,Human_Splice_Rec_693864,Human_Splice_Rec_693865,Human_Splice_Rec_693874,Human_Splice_Rec_693875,Human_Splice_Rec_693882,Human_Splice_Rec_693883,Human_Splice_Rec_693888,Human_Splice_Rec_693894 Human_miRNA_ID_2330834,Human_miRNA_ID_2963917 RMVar_hsa_circ_29887,RMVar_hsa_circ_283499,RMVar_hsa_circ_48904,RMVar_hsa_circ_287214,RMVar_hsa_circ_234638,RMVar_hsa_circ_234639,RMVar_hsa_circ_313789,RMVar_hsa_circ_60451,RMVar_hsa_circ_299188 109671 RMVar_ID_109671 Human_SNP_ID_252476196 m1A Human chr5 - 135360581 135360581 135360581 TGCAAGAAGAAGCAGGGTGAAGTCAGTAAGGCAGCCAGCGCCGACAGCACAACCGAGGGCACACC TGCAAGAAGAAGCAGGGTGAAGTCAGTAAGGCGGCCAGCGCCGACAGCACAACCGAGGGCACACC T C MACROH2A1 Ensembl:ENSG00000113648 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:135360299..135360641 26863196 MeRIP-seq:(Medium) rs765618916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632084,Human_RBP_ID_9398196,Human_RBP_ID_22680708,Human_RBP_ID_22827175 Human_Splice_Rec_693744,Human_Splice_Rec_693745,Human_Splice_Rec_693772,Human_Splice_Rec_693773,Human_Splice_Rec_693788,Human_Splice_Rec_693789,Human_Splice_Rec_693804,Human_Splice_Rec_693805,Human_Splice_Rec_693823,Human_Splice_Rec_693844,Human_Splice_Rec_693845,Human_Splice_Rec_693864,Human_Splice_Rec_693865,Human_Splice_Rec_693874,Human_Splice_Rec_693875,Human_Splice_Rec_693882,Human_Splice_Rec_693883,Human_Splice_Rec_693888,Human_Splice_Rec_693894 Human_miRNA_ID_2330834,Human_miRNA_ID_2963917 RMVar_hsa_circ_29887,RMVar_hsa_circ_283499,RMVar_hsa_circ_48904,RMVar_hsa_circ_287214,RMVar_hsa_circ_234638,RMVar_hsa_circ_234639,RMVar_hsa_circ_313789,RMVar_hsa_circ_60451,RMVar_hsa_circ_299188 109672 RMVar_ID_109672 Human_SNP_ID_252476200 m1A Human chr5 - 135360600 135360600 135360600 ATTCTGACCCTTCCGTCTGTGCAAGAAGAAGCAGGGTGAAGTCAGTAAGGCAGCCAGCGCCGACA ATTCTGACCCTTCCGTCTGTGCAAGAAGAAGCCGGGTGAAGTCAGTAAGGCAGCCAGCGCCGACA T G MACROH2A1 Ensembl:ENSG00000113648 Protein coding CDS GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr5:135360551..135360625;chr5:135360476..135360625;chr5:135360501..135360625 26863196,32194978,32194978 MeRIP-seq:(Medium) rs764236186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9398196,Human_RBP_ID_19126252,Human_RBP_ID_22680708 Human_Splice_Rec_693744,Human_Splice_Rec_693772,Human_Splice_Rec_693788,Human_Splice_Rec_693804,Human_Splice_Rec_693844,Human_Splice_Rec_693864,Human_Splice_Rec_693874,Human_Splice_Rec_693882,Human_Splice_Rec_693888,Human_Splice_Rec_693894 RMVar_hsa_circ_29887,RMVar_hsa_circ_283499,RMVar_hsa_circ_48904,RMVar_hsa_circ_287214,RMVar_hsa_circ_234638,RMVar_hsa_circ_234639,RMVar_hsa_circ_313789,RMVar_hsa_circ_60451,RMVar_hsa_circ_299188 109673 RMVar_ID_109673 Human_SNP_ID_252482260 m1A Human chr5 - 135389069 135389066 135389069 CCACCGCCATGTCGAGCCGCGGTGGGAAGAAGAAGTCCACCAAGACGTCCAGGTCTGCCAAAGCA CCACCGCCATGTCGAGCCGCGGTGGGAAGAAG___TCCACCAAGACGTCCAGGTCTGCCAAAGCA ACTT A MACROH2A1 Ensembl:ENSG00000113648 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs766733082 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1645091,Human_RBP_ID_1987251,Human_RBP_ID_3758272,Human_RBP_ID_4845976,Human_RBP_ID_5121388,Human_RBP_ID_18057296,Human_RBP_ID_26826554 Human_Splice_Rec_693738,Human_Splice_Rec_693766,Human_Splice_Rec_693782,Human_Splice_Rec_693798,Human_Splice_Rec_693816,Human_Splice_Rec_693830,Human_Splice_Rec_693838,Human_Splice_Rec_693858,Human_Splice_Rec_693868,Human_Splice_Rec_693896 RMVar_hsa_circ_313789,RMVar_hsa_circ_305465,RMVar_hsa_circ_234641 109674 RMVar_ID_109674 Human_SNP_ID_252482271 m1A Human chr5 - 135389099 135389099 135389099 CACAGTGTGCTCACTGATCCGCCTCCAGGGCCACCGCCATGTCGAGCCGCGGTGGGAAGAAGAAG CACAGTGTGCTCACTGATCCGCCTCCAGGGCCCCCGCCATGTCGAGCCGCGGTGGGAAGAAGAAG T G MACROH2A1 Ensembl:ENSG00000113648 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr5:135388885..135389174;chr5:135389076..135389100;chr5:135388878..135389184 26863196 MeRIP-seq:(Medium) rs1409346144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1645092,Human_RBP_ID_4845976,Human_RBP_ID_5121388,Human_RBP_ID_9307053,Human_RBP_ID_18057296,Human_RBP_ID_19126256,Human_RBP_ID_26826554 Human_Splice_Rec_693738,Human_Splice_Rec_693766,Human_Splice_Rec_693782,Human_Splice_Rec_693798,Human_Splice_Rec_693816,Human_Splice_Rec_693830,Human_Splice_Rec_693838,Human_Splice_Rec_693858,Human_Splice_Rec_693868,Human_Splice_Rec_693896 RMVar_hsa_circ_313789,RMVar_hsa_circ_305465,RMVar_hsa_circ_234641 109675 RMVar_ID_109675 Human_SNP_ID_252482280 m1A Human chr5 + 135389126 135389126 135389126 GGCGGTGGCCCTGGAGGCGGATCAGTGAGCACACTGTGAAGGCGAGAGGCACACCGGTCAGGGTG GGCGGTGGCCCTGGAGGCGGATCAGTGAGCACGCTGTGAAGGCGAGAGGCACACCGGTCAGGGTG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:135389103..135389198 26863410 MeRIP-seq:(Medium) rs1482423897 Functional Loss SNV dbSNP153 33..33 33 - - - 109676 RMVar_ID_109676 Human_SNP_ID_252482281 m1A Human chr5 - 135389128 135389127 135389129 GCCACCCTGACCGGTGTGCCTCTCGCCTTCACAGTGTGCTCACTGATCCGCCTCCAGGGCCACCG GCCACCCTGACCGGTGTGCCTCTCGCCTTCA__GTGTGCTCACTGATCCGCCTCCAGGGCCACCG CTG C MACROH2A1 Ensembl:ENSG00000113648 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,ALKBH3 KO chr5:135389126..135389150;chr5:135389026..135389193 26863196,26863410 MeRIP-seq:(Medium) rs1222621513 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_4845976,Human_RBP_ID_19126256 109677 RMVar_ID_109677 Human_SNP_ID_252484389 m1A Human chr5 + 135399025 135399025 135399025 CGGGCACCCGCGGCCGGACCCGAGCGGCGGGGACAGGGAGTGCGGCAAGGGGGCCCGCGCGGCAC CGGGCACCCGCGGCCGGACCCGAGCGGCGGGGGCAGGGAGTGCGGCAAGGGGGCCCGCGCGGCAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:135399021..135399200 26863410 MeRIP-seq:(Medium) rs902739828 Functional Loss SNV dbSNP153 33..33 33 - - - 109678 RMVar_ID_109678 Human_SNP_ID_252641945 m1A Human chr5 - 136046488 136046488 136046488 CCCGGGCAGACGGAGGTCATCTCACAGCTGGCAAGGAGGCCCAGGCCTCGTTGCTAGGGGCGAAG CCCGGGCAGACGGAGGTCATCTCACAGCTGGCGAGGAGGCCCAGGCCTCGTTGCTAGGGGCGAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:136046439..136046540 32194978 MeRIP-seq:(Medium) rs1335835715 Functional Loss SNV dbSNP153 33..33 33 - - - 109679 RMVar_ID_109679 Human_SNP_ID_252642086 m1A Human chr5 - 136046937 136046937 136046937 GAGGTGAGGGTCATGCCGTGTTTCAGCTCATCAGTCAGGACTCGCCTGCCCACCATATGGTAGCG GAGGTGAGGGTCATGCCGTGTTTCAGCTCATCGGTCAGGACTCGCCTGCCCACCATATGGTAGCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:136046887..136047037 32194978 MeRIP-seq:(Medium) rs771740493 Functional Loss SNV dbSNP153 33..33 33 - - - 109680 RMVar_ID_109680 Human_SNP_ID_252646540 m1A Human chr5 - 136063405 136063405 136063405 GTTAACAGCCATGTTTAGGGGGAACATGATTTAAAAAGTACATCTCTCTCCCTCCTCCCCCACAT GTTAACAGCCATGTTTAGGGGGAACATGATTTTAAAAGTACATCTCTCTCCCTCCTCCCCCACAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:136063162..136063423 26863196 MeRIP-seq:(Medium) rs904025878 Functional Loss SNV dbSNP153 33..33 33 - - - 109681 RMVar_ID_109681 Human_SNP_ID_252663491 m1A Human chr5 - 136132964 136132960 136132964 CCCTCGCCCGCGCGCGCCGGGGACCCTCACTCACTCGCGAGCCGGCTAGGCGCGCTCTCCCGACG CCCTCGCCCGCGCGCGCCGGGGACCCTCACTC____GCGAGCCGGCTAGGCGCGCTCTCCCGACG CGAGT C SMAD5-AS1 Ensembl:ENSG00000164621 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:136132851..136133035 26863410 MeRIP-seq:(Medium) rs1415606018 Functional Loss DEL dbSNP153 33..36 33 - - - 109682 RMVar_ID_109682 Human_SNP_ID_252667079 m1A Human chr5 + 136147786 136147784 136147787 TGTTAGTGGTTTATTATTATTACCATTATCAAAGGAGTATTATGATTCCTTTGCTTAAGCAATTG TGTTAGTGGTTTATTATTATTACCATTATCA___GAGTATTATGATTCCTTTGCTTAAGCAATTG AAAG A SMAD5 Ensembl:ENSG00000113658 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:136147783..136147858 26863196 MeRIP-seq:(Medium) rs1207234231 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_7387242 RMVar_hsa_circ_91672,RMVar_hsa_circ_234661 109683 RMVar_ID_109683 Human_SNP_ID_252667080 m1A Human chr5 + 136147786 136147786 136147786 TGTTAGTGGTTTATTATTATTACCATTATCAAAGGAGTATTATGATTCCTTTGCTTAAGCAATTG TGTTAGTGGTTTATTATTATTACCATTATCAAGGGAGTATTATGATTCCTTTGCTTAAGCAATTG A G SMAD5 Ensembl:ENSG00000113658 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:136147783..136147858 26863196 MeRIP-seq:(Medium) rs550504799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7387242 RMVar_hsa_circ_91672,RMVar_hsa_circ_234661 109684 RMVar_ID_109684 Human_SNP_ID_252670086 m1A Human chr5 - 136160980 136160980 136160980 AAGGGAAAAGGAGTGTTGTTGGGCTGGTGGAAAGAATCTGGAAACGTGGCATTTTGTGGCATGTG AAGGGAAAAGGAGTGTTGTTGGGCTGGTGGAAGGAATCTGGAAACGTGGCATTTTGTGGCATGTG T C lnc-SMIM32-5 RNACentral:URS00008BE6BE lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:136160929..136161022 26863196 MeRIP-seq:(Medium) rs750737161 Functional Loss SNV dbSNP153 33..33 33 - - - 109685 RMVar_ID_109685 Human_SNP_ID_252676361 m1A Human chr5 - 136187919 136187919 136187919 CTACTCCTGTCTATGTCCACCATCACAACCCTAACTCAAAGCCCTACTTCCATTTTTGTCTCTCC CTACTCCTGTCTATGTCCACCATCACAACCCTGACTCAAAGCCCTACTTCCATTTTTGTCTCTCC T C lnc-SMIM32-4,lnc-SMIM32-4:2 RNACentral:URS0000D6E8CF,RNACentral:URS0000D6DB62 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:136187872..136187990 26863196 MeRIP-seq:(Medium) rs1385019364 Functional Loss SNV dbSNP153 33..33 33 - - - 109686 RMVar_ID_109686 Human_SNP_ID_252865452 m1A Human chr5 + 136979291 136979291 136979291 AGAGATCCTTATGCAGTGAGGAACCACAGGCCACCCAGGTCATTGTGGGGCTCATGCAGGAGGCC AGAGATCCTTATGCAGTGAGGAACCACAGGCCTCCCAGGTCATTGTGGGGCTCATGCAGGAGGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:136979288..136979432 26863196 MeRIP-seq:(Medium) rs1159062614 Functional Loss SNV dbSNP153 33..33 33 - - - 109687 RMVar_ID_109687 Human_SNP_ID_252951752 m1A Human chr5 + 137354069 137354069 137354069 GCCACCATTTTCACTCACGTTCTGACCCTCAGAAGCTCTGAAATCACATCTCCCTGACTCCAACA GCCACCATTTTCACTCACGTTCTGACCCTCAGCAGCTCTGAAATCACATCTCCCTGACTCCAACA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:137354067..137354186 26863196 MeRIP-seq:(Medium) rs1039568442 Functional Loss SNV dbSNP153 33..33 33 - - - 109688 RMVar_ID_109688 Human_SNP_ID_252969131 m1A Human chr5 + 137428677 137428677 137428677 GGCATTAAGTTCTCCCTCAATGTCCTGCTGCCAAACTGTGGGTCCCCTCTGGCTCTCCTCACTGG GGCATTAAGTTCTCCCTCAATGTCCTGCTGCCGAACTGTGGGTCCCCTCTGGCTCTCCTCACTGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:137428673..137428859 26863196 MeRIP-seq:(Medium) rs929715213 Functional Loss SNV dbSNP153 33..33 33 - - - 109689 RMVar_ID_109689 Human_SNP_ID_253043684 m1A Human chr5 + 137753376 137753349 137753376 CGAACCGCCGCCGCCGCCTCCGTAGGCATTGTAGCCGCCGCCTCCGCCGCCGCCGTAACCACCGT CGAACC___________________________GCCGCCGCCTCCGCCGCCGCCGTAACCACCGT CGCCGCCGCCGCCTCCGTAGGCATTGTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:137752851..137754376;chr5:137752826..137754400 26863196 MeRIP-seq:(Medium) rs1243649594 Functional Loss DEL dbSNP153 7..33 33 - - - 109690 RMVar_ID_109690 Human_SNP_ID_253043688 m1A Human chr5 + 137753376 137753352 137753376 CGAACCGCCGCCGCCGCCTCCGTAGGCATTGTAGCCGCCGCCTCCGCCGCCGCCGTAACCACCGT CGAACCGCC________________________GCCGCCGCCTCCGCCGCCGCCGTAACCACCGT CGCCGCCGCCTCCGTAGGCATTGTA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:137752851..137754376;chr5:137752826..137754400 26863196 MeRIP-seq:(Medium) rs1455105054 Functional Loss DEL dbSNP153 10..33 33 - - - 109691 RMVar_ID_109691 Human_SNP_ID_253043736 m1A Human chr5 - 137753412 137753410 137753412 GCCTTTCCAAGGGCGGCGGCGGCGGTTACAACAGCTACGGTGGTTACGGCGGCGGCGGAGGCGGC GCCTTTCCAAGGGCGGCGGCGGCGGTTACAAC__CTACGGTGGTTACGGCGGCGGCGGAGGCGGC GCT G HNRNPA0 Ensembl:ENSG00000177733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:137752912..137754376 26863196 MeRIP-seq:(Medium) rs967457161 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1039076,Human_RBP_ID_4849749,Human_RBP_ID_18039358,Human_RBP_ID_22099611,Human_RBP_ID_22295852,Human_RBP_ID_22459729,Human_RBP_ID_22511508,Human_RBP_ID_27074241,Human_RBP_ID_27331524 RMVar_hsa_circ_234697,RMVar_hsa_circ_234692,RMVar_hsa_circ_234698 109692 RMVar_ID_109692 Human_SNP_ID_253043755 m1A Human chr5 - 137753435 137753435 137753435 CGGCGGTGGTCGAGACCAGAACGGCCTTTCCAAGGGCGGCGGCGGCGGTTACAACAGCTACGGTG CGGCGGTGGTCGAGACCAGAACGGCCTTTCCACGGGCGGCGGCGGCGGTTACAACAGCTACGGTG T G HNRNPA0 Ensembl:ENSG00000177733 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr5:137753129..137753550;chr5:137752851..137754375 26863410,26863196 MeRIP-seq:(Medium) rs1216276467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632408,Human_RBP_ID_1039076,Human_RBP_ID_4810533,Human_RBP_ID_7387940,Human_RBP_ID_17671723,Human_RBP_ID_17707037,Human_RBP_ID_18039358,Human_RBP_ID_22099611,Human_RBP_ID_22459283,Human_RBP_ID_22511509,Human_RBP_ID_27511615 RMVar_hsa_circ_234697,RMVar_hsa_circ_234692,RMVar_hsa_circ_234698 109693 RMVar_ID_109693 Human_SNP_ID_253043801 m1A Human chr5 - 137753512 137753512 137753512 CCCAAGGAGGATATCTACTCCGGTGGGGGTGGAGGCGGCTCCCGATCCTCCCGGGGCGGCCGAGG CCCAAGGAGGATATCTACTCCGGTGGGGGTGGGGGCGGCTCCCGATCCTCCCGGGGCGGCCGAGG T C HNRNPA0 Ensembl:ENSG00000177733 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:137753201..137753625;chr5:137753326..137753630 26863196 MeRIP-seq:(Medium) rs1302300558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78676,Human_RBP_ID_632411,Human_RBP_ID_1039079,Human_RBP_ID_1069499,Human_RBP_ID_5151634,Human_RBP_ID_9335340,Human_RBP_ID_17707038,Human_RBP_ID_18039359,Human_RBP_ID_22099612,Human_RBP_ID_22458922 RMVar_hsa_circ_234697,RMVar_hsa_circ_234692,RMVar_hsa_circ_234698,RMVar_hsa_circ_234700 109694 RMVar_ID_109694 Human_SNP_ID_253044006 m1A Human chr5 + 137754210 137754210 137754210 ACCCCCGCCGCTCACCGACGGGGAAGGGAAAAAGGGAAGGGGAGGGAAGGAAGGAAGAGAGGAAG ACCCCCGCCGCTCACCGACGGGGAAGGGAAAAGGGGAAGGGGAGGGAAGGAAGGAAGAGAGGAAG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:137754162..137754375 26863196 MeRIP-seq:(Medium) rs1293483562 Functional Loss SNV dbSNP153 33..33 33 - - - 109695 RMVar_ID_109695 Human_SNP_ID_253044042 m1A Human chr5 + 137754286 137754286 137754286 GGGAGCGGTGCCGGCTAAAGGGCGAGCCGAGGAGACTGGAAGACAACCAAGGCCACCGCTACCGC GGGAGCGGTGCCGGCTAAAGGGCGAGCCGAGGGGACTGGAAGACAACCAAGGCCACCGCTACCGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:137754201..137754350 26863410 MeRIP-seq:(Medium) rs1177410548 Functional Loss SNV dbSNP153 33..33 33 - - - 109696 RMVar_ID_109696 Human_SNP_ID_253094301 m1A Human chr5 + 137975266 137975266 137975266 CCCCTCTTCTGCAACTTCTTCACCTTACTGTCACCGCTTGAAAACTTCATTCTAAATTTCTAATC CCCCTCTTCTGCAACTTCTTCACCTTACTGTCTCCGCTTGAAAACTTCATTCTAAATTTCTAATC A T RF00017-4544 RNACentral:URS000093ECB5 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:137975218..137975340 26863196 MeRIP-seq:(Medium) rs1052506085 Functional Loss SNV dbSNP153 33..33 33 - - - 109697 RMVar_ID_109697 Human_SNP_ID_253108489 m1A Human chr5 - 138033017 138033017 138033017 GGCTCTGCACCTCAGCCGCCGCCTCTGTCGCCACTCTCTCCCCCTGTTCCGCGTCTGCGTCGCCA GGCTCTGCACCTCAGCCGCCGCCTCTGTCGCCCCTCTCTCCCCCTGTTCCGCGTCTGCGTCGCCA T G FAM13B Ensembl:ENSG00000031003 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:138032869..138036255 26863410 MeRIP-seq:(Medium) rs1449002261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4810651,Human_RBP_ID_5426884,Human_RBP_ID_5449328,Human_RBP_ID_5476238,Human_RBP_ID_9335344,Human_RBP_ID_27331566 RMVar_hsa_circ_118587,RMVar_hsa_circ_234727 109698 RMVar_ID_109698 Human_SNP_ID_253108491 m1A Human chr5 + 138033022 138033021 138033023 ACGCAGACGCGGAACAGGGGGAGAGAGTGGCGACAGAGGCGGCGGCTGAGGTGCAGAGCCTCCCT ACGCAGACGCGGAACAGGGGGAGAGAGTGGCG__AGAGGCGGCGGCTGAGGTGCAGAGCCTCCCT GAC G AC113382.1 Ensembl:ENSG00000246323 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138032821..138036255 26863196 MeRIP-seq:(Medium) rs1336266931 Functional Loss DEL dbSNP153 33..34 33 - - - 109699 RMVar_ID_109699 Human_SNP_ID_253140310 m1A Human chr5 - 138164946 138164946 138164946 AACGGAAAACAAGGGAATACATGAACTGGTGGACATCAGGGAGCCCAGTGCAGAGATCAAGGTGG AACGGAAAACAAGGGAATACATGAACTGGTGGGCATCAGGGAGCCCAGTGCAGAGATCAAGGTGG T C BRD8 Ensembl:ENSG00000112983 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138164396..138164946 32194978 MeRIP-seq:(Medium) rs142694367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249883,Human_RBP_ID_943460,Human_RBP_ID_1645340,Human_RBP_ID_1987560,Human_RBP_ID_3967412,Human_RBP_ID_5532026,Human_RBP_ID_7388819,Human_RBP_ID_8236963,Human_RBP_ID_8603616,Human_RBP_ID_8884625,Human_RBP_ID_17662579,Human_RBP_ID_18425167,Human_RBP_ID_19015102,Human_RBP_ID_24548004,Human_RBP_ID_26351320,Human_RBP_ID_27074316,Human_RBP_ID_27825837 Human_miRNA_ID_2553132,Human_miRNA_ID_2553133,Human_miRNA_ID_3000880,Human_miRNA_ID_3000881 RMVar_hsa_circ_505,RMVar_hsa_circ_29425,RMVar_hsa_circ_81575,RMVar_hsa_circ_368180,RMVar_hsa_circ_234753,RMVar_hsa_circ_234752,RMVar_hsa_circ_234755,RMVar_hsa_circ_364886,RMVar_hsa_circ_102696,RMVar_hsa_circ_93708,RMVar_hsa_circ_58688,RMVar_hsa_circ_234757 109700 RMVar_ID_109700 Human_SNP_ID_253144134 m1A Human chr5 - 138179199 138179199 138179199 CCCGGGCTCCAGCACAGCCGCACACTCACCCGAAGACGTGCCACTTGCTCCTCCTGGGATACTGG CCCGGGCTCCAGCACAGCCGCACACTCACCCGGAGACGTGCCACTTGCTCCTCCTGGGATACTGG T C RF00017-4706 RNACentral:URS0000954994 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138179151..138179264 26863196 MeRIP-seq:(Medium) rs1561627079 Functional Loss SNV dbSNP153 33..33 33 - - - 109701 RMVar_ID_109701 Human_SNP_ID_253152946 m1A Human chr5 + 138213280 138213280 138213280 ATGGACAGGACAGGCGCCACTGCCGCCGTCACAGCCACCGGGACCATGGAGGTACTCGCAGCCAT ATGGACAGGACAGGCGCCACTGCCGCCGTCACTGCCACCGGGACCATGGAGGTACTCGCAGCCAT A T RF00017-4489,RF00017-4544 RNACentral:URS00009982F9,RNACentral:URS000093ECB5 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138213200..138213289 26863196 MeRIP-seq:(Medium) rs199790979 Functional Loss SNV dbSNP153 33..33 33 - - - 109702 RMVar_ID_109702 Human_SNP_ID_253152956 m1A Human chr5 + 138213290 138213290 138213290 CAGGCGCCACTGCCGCCGTCACAGCCACCGGGACCATGGAGGTACTCGCAGCCATTTTCCCGACT CAGGCGCCACTGCCGCCGTCACAGCCACCGGGGCCATGGAGGTACTCGCAGCCATTTTCCCGACT A G RF00017-4489,RF00017-4544 RNACentral:URS00009982F9,RNACentral:URS000093ECB5 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138213176..138213325 26863196 MeRIP-seq:(Medium) rs1383146807 Functional Loss SNV dbSNP153 33..33 33 - - - 109703 RMVar_ID_109703 Human_SNP_ID_253170916 m1A Human chr5 - 138286135 138286135 138286135 TTCCACCCCACCCATCTCTGGGTTCTCTCTAAAGGTGCCGCTGTCTGCGTGAAGAGGACAGGTCT TTCCACCCCACCCATCTCTGGGTTCTCTCTAAGGGTGCCGCTGTCTGCGTGAAGAGGACAGGTCT T C CDC25C Ensembl:ENSG00000158402 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138286093..138289507 32194978 MeRIP-seq:(Medium) rs1488696040 Functional Loss SNV dbSNP153 33..33 33 - - - 109704 RMVar_ID_109704 Human_SNP_ID_253172409 m1A Human chr5 - 138292110 138292110 138292110 CTAGGGGGTTTAATATTCCCAAACAGGTGAGCAGAAGTGGCCTATATCGCTCCCCGTCGATGCCA CTAGGGGGTTTAATATTCCCAAACAGGTGAGCTGAAGTGGCCTATATCGCTCCCCGTCGATGCCA T A CDC25C Ensembl:ENSG00000158402 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138292059..138319262 32194978 MeRIP-seq:(Medium) rs1046133488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_942994,Human_RBP_ID_26352568 Human_Splice_Rec_696086,Human_Splice_Rec_696112,Human_Splice_Rec_696132,Human_Splice_Rec_696162,Human_Splice_Rec_696188,Human_Splice_Rec_696210,Human_Splice_Rec_696248 RMVar_hsa_circ_46532,RMVar_hsa_circ_27485,RMVar_hsa_circ_234774,RMVar_hsa_circ_369906,RMVar_hsa_circ_344821,RMVar_hsa_circ_234775 109705 RMVar_ID_109705 Human_SNP_ID_253175062 m1A Human chr5 - 138303574 138303574 138303574 AGATGTCAGGAGGAATGAGTCATTCCCAGCAGAAGGCAAAGCAAGTGCAATGCCCCTGAGGTGAG AGATGTCAGGAGGAATGAGTCATTCCCAGCAGGAGGCAAAGCAAGTGCAATGCCCCTGAGGTGAG T C CDC25C Ensembl:ENSG00000158402 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:138303563..138303673 26863196 MeRIP-seq:(Medium) rs541715207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_696161 RMVar_hsa_circ_46532,RMVar_hsa_circ_27485,RMVar_hsa_circ_234775 109706 RMVar_ID_109706 Human_SNP_ID_253183539 m1A Human chr5 - 138338295 138338295 138338295 ACCTGCCCTCCACCACCTACCGCGGTTCCTCCAGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG ACCTGCCCTCCACCACCTACCGCGGTTCCTCCTGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG T A CDC25C Ensembl:ENSG00000158402 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138338194..138338294 32194978 MeRIP-seq:(Medium) rs568177872 Functional Loss SNV dbSNP153 33..33 33 - - - 109707 RMVar_ID_109707 Human_SNP_ID_253183540 m1A Human chr5 - 138338295 138338295 138338295 ACCTGCCCTCCACCACCTACCGCGGTTCCTCCAGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG ACCTGCCCTCCACCACCTACCGCGGTTCCTCCGGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG T C CDC25C Ensembl:ENSG00000158402 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138338194..138338294 32194978 MeRIP-seq:(Medium) rs568177872 Functional Loss SNV dbSNP153 33..33 33 - - - 109708 RMVar_ID_109708 Human_SNP_ID_253183541 m1A Human chr5 - 138338295 138338295 138338295 ACCTGCCCTCCACCACCTACCGCGGTTCCTCCAGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG ACCTGCCCTCCACCACCTACCGCGGTTCCTCCCGCTCCCAGGGCCGCGGCCGGAGCAGCTCTGAG T G CDC25C Ensembl:ENSG00000158402 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138338194..138338294 32194978 MeRIP-seq:(Medium) rs568177872 Functional Loss SNV dbSNP153 33..33 33 - - - 109709 RMVar_ID_109709 Human_SNP_ID_253183561 m1A Human chr5 - 138338309 138338309 138338309 GAGGCCCCAGCGCCACCTGCCCTCCACCACCTACCGCGGTTCCTCCAGCTCCCAGGGCCGCGGCC GAGGCCCCAGCGCCACCTGCCCTCCACCACCTGCCGCGGTTCCTCCAGCTCCCAGGGCCGCGGCC T C CDC25C Ensembl:ENSG00000158402 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:138338295..138338433;chr5:138338295..138338386 26863196 MeRIP-seq:(Medium) rs773410448 Functional Loss SNV dbSNP153 33..33 33 - - - 109710 RMVar_ID_109710 Human_SNP_ID_253184341 m1A Human chr5 - 138341186 138341186 138341186 ATTGGGACTTCCCTCTCCAGTCATGCCTGCTGAGTCTGCCAATTAGAGGGACCAGCCCCAAGTGA ATTGGGACTTCCCTCTCCAGTCATGCCTGCTGGGTCTGCCAATTAGAGGGACCAGCCCCAAGTGA T C RF00017-4575,RF00017-4706 RNACentral:URS0000918622,RNACentral:URS0000954994 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:138341181..138341296 26863196 MeRIP-seq:(Medium) rs560953062 Functional Loss SNV dbSNP153 33..33 33 - - - 109711 RMVar_ID_109711 Human_SNP_ID_253184349 m1A Human chr5 + 138341205 138341205 138341205 CTAATTGGCAGACTCAGCAGGCATGACTGGAGAGGGAAGTCCCAATGGTGCTAGAATGGTGCTGC CTAATTGGCAGACTCAGCAGGCATGACTGGAGTGGGAAGTCCCAATGGTGCTAGAATGGTGCTGC A T FAM53C Ensembl:ENSG00000120709 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:138341201..138341297 26863196 MeRIP-seq:(Medium) rs916040144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250034,Human_RBP_ID_632526,Human_RBP_ID_1390206,Human_RBP_ID_1645411,Human_RBP_ID_4849864,Human_RBP_ID_7389330,Human_RBP_ID_15312953,Human_RBP_ID_22827235,Human_RBP_ID_26352569 Human_Splice_Rec_696282,Human_Splice_Rec_696298,Human_Splice_Rec_696300,Human_Splice_Rec_696308,Human_Splice_Rec_696316,Human_Splice_Rec_696317 Human_miRNA_ID_749016,Human_miRNA_ID_2306348,Human_miRNA_ID_2955335 RMVar_hsa_circ_2253,RMVar_hsa_circ_103165,RMVar_hsa_circ_234778 109712 RMVar_ID_109712 Human_SNP_ID_253195650 m1A Human chr5 + 138386552 138386552 138386552 GCCAGCTCCACCCCAAACACAGTGAGGATCTCAGACACTGGCCTTGCAGCAGGGACTGTGCCAGA GCCAGCTCCACCCCAAACACAGTGAGGATCTCGGACACTGGCCTTGCAGCAGGGACTGTGCCAGA A G KDM3B Ensembl:ENSG00000120733 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:138386501..138386575 32194978 MeRIP-seq:(Medium) rs1218285220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4811228,Human_RBP_ID_8884755,Human_RBP_ID_15313608,Human_RBP_ID_19015898 Human_Splice_Rec_696337,Human_Splice_Rec_696383,Human_Splice_Rec_696455 Human_miRNA_ID_506782,Human_miRNA_ID_513982,Human_miRNA_ID_1095183,Human_miRNA_ID_2174739,Human_miRNA_ID_2178182,Human_miRNA_ID_2511221,Human_miRNA_ID_3054044 RMVar_hsa_circ_127068,RMVar_hsa_circ_333982,RMVar_hsa_circ_337255,RMVar_hsa_circ_298118,RMVar_hsa_circ_265165,RMVar_hsa_circ_84712,RMVar_hsa_circ_90641,RMVar_hsa_circ_18866,RMVar_hsa_circ_21216,RMVar_hsa_circ_234782,RMVar_hsa_circ_234783,RMVar_hsa_circ_234780,RMVar_hsa_circ_234781,RMVar_hsa_circ_302481,RMVar_hsa_circ_234779,RMVar_hsa_circ_286716,RMVar_hsa_circ_234789,RMVar_hsa_circ_93949,RMVar_hsa_circ_369169,RMVar_hsa_circ_335466,RMVar_hsa_circ_64879,RMVar_hsa_circ_234793,RMVar_hsa_circ_362319,RMVar_hsa_circ_365540,RMVar_hsa_circ_366650,RMVar_hsa_circ_125062,RMVar_hsa_circ_305467,RMVar_hsa_circ_65067,RMVar_hsa_circ_234794,RMVar_hsa_circ_335250,RMVar_hsa_circ_369170,RMVar_hsa_circ_234792,RMVar_hsa_circ_361717,RMVar_hsa_circ_331159,RMVar_hsa_circ_234796,RMVar_hsa_circ_115877,RMVar_hsa_circ_123150,RMVar_hsa_circ_234795,RMVar_hsa_circ_234797 109713 RMVar_ID_109713 Human_SNP_ID_253210764 m1A Human chr5 + 138446536 138446536 138446536 CTCAACCCTCCATCCTAGGCTCTGAGCCTCAGAGGACCCAGCCCATGAGAGAACGGGGATCTGGG CTCAACCCTCCATCCTAGGCTCTGAGCCTCAGGGGACCCAGCCCATGAGAGAACGGGGATCTGGG A G REEP2 Ensembl:ENSG00000132563 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:138446421..138446571 32194978 MeRIP-seq:(Medium) rs946443224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22511558 109714 RMVar_ID_109714 Human_SNP_ID_253215554 m1A Human chr5 + 138465520 138465519 138465521 CAGCGCGCAGAACTTGGGGAGCCGCCGCCGCCATCCGCCGCCGCAGCCAGCTTCCGCCGCCGCAG CAGCGCGCAGAACTTGGGGAGCCGCCGCCGCC__CCGCCGCCGCAGCCAGCTTCCGCCGCCGCAG CAT C EGR1 Ensembl:ENSG00000120738 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:138465511..138465683 26863196 MeRIP-seq:(Medium) rs144720042 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_944562,Human_RBP_ID_4811510,Human_RBP_ID_22534027,Human_RBP_ID_26351337,Human_RBP_ID_27826800 109715 RMVar_ID_109715 Human_SNP_ID_253215556 m1A Human chr5 - 138465539 138465520 138465539 GCTGGGGCAGGGGCCGGTCCTGCGGCGGCGGAAGCTGGCTGCGGCGGCGGATGGCGGCGGCGGCT GCTGGGGCAGGGGCCGGTCCTGCGGCGGCGGA___________________TGGCGGCGGCGGCT ATCCGCCGCCGCAGCCAGCT A RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:138465500..138465674 26863196 MeRIP-seq:(Medium) rs1176905028 Functional Loss DEL dbSNP153 33..51 33 - - - 109716 RMVar_ID_109716 Human_SNP_ID_253215588 m1A Human chr5 - 138465639 138465639 138465639 CGGGTTACATGCGGGGCGCGGGGAACACTGAGAAGCGTGCAGGCGGCGACCCCGACTCGCCCTGG CGGGTTACATGCGGGGCGCGGGGAACACTGAGCAGCGTGCAGGCGGCGACCCCGACTCGCCCTGG T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:138465553..138465658 26863410 MeRIP-seq:(Medium) rs536813492 Functional Loss SNV dbSNP153 33..33 33 - - - 109717 RMVar_ID_109717 Human_SNP_ID_253215809 m1A Human chr5 + 138465993 138465988 138465994 GCGGGGGCGGTGGAGGCGGCGGGGGCGGCAGCAACAGCAGCAGCAGCAGCAGCACCTTCAACCCT GCGGGGGCGGTGGAGGCGGCGGGGGCGG______CAGCAGCAGCAGCAGCAGCACCTTCAACCCT GCAGCAA G EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:138465951..138466050 26863196 MeRIP-seq:(Medium) rs1463434819 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_78092,Human_RBP_ID_943466,Human_RBP_ID_4811524 Human_Splice_Rec_696603 109718 RMVar_ID_109718 Human_SNP_ID_253215809 m1A Human chr5 + 138465994 138465988 138465994 CGGGGGCGGTGGAGGCGGCGGGGGCGGCAGCAACAGCAGCAGCAGCAGCAGCACCTTCAACCCTC CGGGGGCGGTGGAGGCGGCGGGGGCGG______CAGCAGCAGCAGCAGCAGCACCTTCAACCCTC GCAGCAA G EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:138465873..138466071;chr5:138465900..138466060 26863196 MeRIP-seq:(Medium) rs1463434819 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_78092,Human_RBP_ID_943466,Human_RBP_ID_4811524 Human_Splice_Rec_696603 109719 RMVar_ID_109719 Human_SNP_ID_253215812 m1A Human chr5 + 138465994 138465994 138465994 CGGGGGCGGTGGAGGCGGCGGGGGCGGCAGCAACAGCAGCAGCAGCAGCAGCACCTTCAACCCTC CGGGGGCGGTGGAGGCGGCGGGGGCGGCAGCAGCAGCAGCAGCAGCAGCAGCACCTTCAACCCTC A G EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:138465873..138466071;chr5:138465900..138466060 26863196 MeRIP-seq:(Medium) rs1561813866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78092,Human_RBP_ID_943466,Human_RBP_ID_4811524 Human_Splice_Rec_696603 109720 RMVar_ID_109720 Human_SNP_ID_253216142 m1A Human chr5 - 138466963 138466963 138466963 GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGACGAGGAGGCCGGTGGGTTGGTCATGCTCACTA GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGTCGAGGAGGCCGGTGGGTTGGTCATGCTCACTA T A RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138466773..138467193 26863196 MeRIP-seq:(Medium) rs201570244 Functional Loss SNV dbSNP153 33..33 33 - - - 109721 RMVar_ID_109721 Human_SNP_ID_253216143 m1A Human chr5 - 138466963 138466963 138466963 GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGACGAGGAGGCCGGTGGGTTGGTCATGCTCACTA GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGGCGAGGAGGCCGGTGGGTTGGTCATGCTCACTA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138466773..138467193 26863196 MeRIP-seq:(Medium) rs201570244 Functional Loss SNV dbSNP153 33..33 33 - - - 109722 RMVar_ID_109722 Human_SNP_ID_253216144 m1A Human chr5 - 138466963 138466963 138466963 GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGACGAGGAGGCCGGTGGGTTGGTCATGCTCACTA GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGCCGAGGAGGCCGGTGGGTTGGTCATGCTCACTA T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138466773..138467193 26863196 MeRIP-seq:(Medium) rs201570244 Functional Loss SNV dbSNP153 33..33 33 - - - 109723 RMVar_ID_109723 Human_SNP_ID_253216148 m1A Human chr5 + 138466968 138466968 138466968 AGCATGACCAACCCACCGGCCTCCTCGTCCTCAGCACCATCTCCAGCGGCCTCCTCCGCCTCCGC AGCATGACCAACCCACCGGCCTCCTCGTCCTCGGCACCATCTCCAGCGGCCTCCTCCGCCTCCGC A G EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138465476..138467175 26863196 MeRIP-seq:(Medium) rs199903799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17532355,Human_RBP_ID_26521853 Human_miRNA_ID_100906 109724 RMVar_ID_109724 Human_SNP_ID_253216189 m1A Human chr5 + 138467080 138467080 138467080 GTCCCATTTACTCAGCGGCACCCACCTTCCCCACGCCGAACACTGACATTTTCCCTGAGCCACAA GTCCCATTTACTCAGCGGCACCCACCTTCCCCCCGCCGAACACTGACATTTTCCCTGAGCCACAA A C EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:138466851..138467208 26863196 MeRIP-seq:(Medium) rs201793207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17303450,Human_RBP_ID_17415583,Human_RBP_ID_22099664,Human_RBP_ID_26351342,Human_RBP_ID_27511757 109725 RMVar_ID_109725 Human_SNP_ID_253216451 m1A Human chr5 + 138467836 138467836 138467836 CCCCGGTTACTACCTCTTATCCATCCCCGGCCACCACCTCATACCCATCCCCTGTGCCCACCTCC CCCCGGTTACTACCTCTTATCCATCCCCGGCCGCCACCTCATACCCATCCCCTGTGCCCACCTCC A G EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr5:138467756..138468038;chr5:138467785..138467964 26863196 MeRIP-seq:(Medium) rs767650411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788700,Human_RBP_ID_3783766,Human_RBP_ID_5133850,Human_RBP_ID_17090103,Human_RBP_ID_17575755,Human_RBP_ID_18956134,Human_RBP_ID_27511766 109726 RMVar_ID_109726 Human_SNP_ID_253216476 m1A Human chr5 - 138467918 138467918 138467918 AGGAGTACGTGGTGGCCACCGACGGGGAGGGGAAGCCACTGTGCACAGGGGATGGGTAGGTCGAG AGGAGTACGTGGTGGCCACCGACGGGGAGGGGCAGCCACTGTGCACAGGGGATGGGTAGGTCGAG T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:138467870..138467971 32194978 MeRIP-seq:(Medium) rs1286256447 Functional Loss SNV dbSNP153 33..33 33 - - - 109727 RMVar_ID_109727 Human_SNP_ID_253232250 m1A Human chr5 + 138529614 138529613 138529614 GGCCTCTGCACTCAGATTCTCTTCTTGTTCTCATTGGTTTTAGGGGCACTTTGGCTTATCAAAGC GGCCTCTGCACTCAGATTCTCTTCTTGTTCTC_TTGGTTTTAGGGGCACTTTGGCTTATCAAAGC CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138529611..138529689 26863196 MeRIP-seq:(Medium) rs1200086570 Functional Loss DEL dbSNP153 33..33 33 - - - 109728 RMVar_ID_109728 Human_SNP_ID_253239332 m1A Human chr5 + 138555518 138555516 138555518 GTTTTAATAGCTGTACCTAATATAAATAGCTAAGTTTCCCATTGTTCTAGATTCCTCTGCCCCAT GTTTTAATAGCTGTACCTAATATAAATAGCT__GTTTCCCATTGTTCTAGATTCCTCTGCCCCAT TAA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138555475..138555773 32194978 MeRIP-seq:(Medium) rs938556479 Functional Loss DEL dbSNP153 32..33 33 - - - 109729 RMVar_ID_109729 Human_SNP_ID_253239456 m1A Human chr5 - 138556008 138556008 138556008 GTAATAATAGCAGAAATTTTGAAGCCAGAAGGACAACATATGAAGCTTAGGAGTGAAGAGACTTC GTAATAATAGCAGAAATTTTGAAGCCAGAAGGGCAACATATGAAGCTTAGGAGTGAAGAGACTTC T C HSPA9 Ensembl:ENSG00000113013 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138555970..138556785 32194978 MeRIP-seq:(Medium) rs765294292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632737,Human_RBP_ID_1987815,Human_RBP_ID_2898341,Human_RBP_ID_7390163,Human_RBP_ID_9398261,Human_RBP_ID_9444267,Human_RBP_ID_15315156,Human_RBP_ID_18039748,Human_RBP_ID_18538718,Human_RBP_ID_27074576,Human_RBP_ID_27825870 Human_miRNA_ID_656091,Human_miRNA_ID_2254403 RMVar_hsa_circ_91150,RMVar_hsa_circ_98621,RMVar_hsa_circ_234832,RMVar_hsa_circ_234833 109730 RMVar_ID_109730 Human_SNP_ID_253239707 m1A Human chr5 + 138556844 138556844 138556844 TGGTTTCTGTGTCGTGAATGATTCCTTCAGCCATATTAACTGCTTCAACTCGTTCCTTAGAGAAA TGGTTTCTGTGTCGTGAATGATTCCTTCAGCCGTATTAACTGCTTCAACTCGTTCCTTAGAGAAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138556743..138556899 26863196 MeRIP-seq:(Medium) rs201621668 Functional Loss SNV dbSNP153 33..33 33 - - - 109731 RMVar_ID_109731 Human_SNP_ID_253240040 m1A Human chr5 + 138557921 138557921 138557921 CCTTTATCTTTAGCAGAAACATGTACTATCCCATTGGCATCAATGTCAAATGTAACTTCAATCTG CCTTTATCTTTAGCAGAAACATGTACTATCCCGTTGGCATCAATGTCAAATGTAACTTCAATCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138557825..138557985 26863196 MeRIP-seq:(Medium) rs533231313 Functional Loss SNV dbSNP153 33..33 33 - - - 109732 RMVar_ID_109732 Human_SNP_ID_253240605 m1A Human chr5 - 138559977 138559977 138559977 CCATTCAGGGAGGTGTGTTGGCCGGCGATGTCACGGATGTGCTGCTCCTTGATGTCACTCCCCTG CCATTCAGGGAGGTGTGTTGGCCGGCGATGTCCCGGATGTGCTGCTCCTTGATGTCACTCCCCTG T G HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138559927..138560004 26863196 MeRIP-seq:(Medium) rs1197264791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249892,Human_RBP_ID_787548,Human_RBP_ID_1987844,Human_RBP_ID_3967436,Human_RBP_ID_4850107,Human_RBP_ID_7390203,Human_RBP_ID_8884918,Human_RBP_ID_9262292,Human_RBP_ID_9306624,Human_RBP_ID_9398275,Human_RBP_ID_17707090,Human_RBP_ID_18056889,Human_RBP_ID_22100693,Human_RBP_ID_22458940,Human_RBP_ID_24085309,Human_RBP_ID_27074609,Human_RBP_ID_27826825 Human_miRNA_ID_2098946,Human_miRNA_ID_2104895,Human_miRNA_ID_2110846,Human_miRNA_ID_2163392,Human_miRNA_ID_2594611,Human_miRNA_ID_2721554,Human_miRNA_ID_2737558,Human_miRNA_ID_2902296,Human_miRNA_ID_3038155 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_26156,RMVar_hsa_circ_70390,RMVar_hsa_circ_272810,RMVar_hsa_circ_56353,RMVar_hsa_circ_54952,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_13526,RMVar_hsa_circ_234834,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_359496,RMVar_hsa_circ_234835,RMVar_hsa_circ_269350,RMVar_hsa_circ_85314,RMVar_hsa_circ_272831,RMVar_hsa_circ_370666,RMVar_hsa_circ_234837,RMVar_hsa_circ_285035,RMVar_hsa_circ_127829,RMVar_hsa_circ_77999,RMVar_hsa_circ_234838,RMVar_hsa_circ_234840,RMVar_hsa_circ_234842,RMVar_hsa_circ_54836,RMVar_hsa_circ_234843,RMVar_hsa_circ_234841,RMVar_hsa_circ_234839 109733 RMVar_ID_109733 Human_SNP_ID_253241697 m1A Human chr5 + 138563463 138563463 138563463 TCACAATGTTCTTTCCTTACCCTCCTCTCTCAAACCCAATCACTTGTGTCTTACTCTCACTCTCA TCACAATGTTCTTTCCTTACCCTCCTCTCTCAGACCCAATCACTTGTGTCTTACTCTCACTCTCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:138563425..138563534 26863196 MeRIP-seq:(Medium) rs1418725402 Functional Loss SNV dbSNP153 33..33 33 - - - 109734 RMVar_ID_109734 Human_SNP_ID_253242527 m1A Human chr5 - 138566691 138566691 138566691 TATAGACAGGGGTTGATTTGACTAAAGACAACATGGCACTTCAGAGGGTACGGGAAGCTGCTGAA TATAGACAGGGGTTGATTTGACTAAAGACAACCTGGCACTTCAGAGGGTACGGGAAGCTGCTGAA T G HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138566640..138567121 32194978 MeRIP-seq:(Medium) rs774485873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74187,Human_RBP_ID_1645656,Human_RBP_ID_1987856,Human_RBP_ID_3759010,Human_RBP_ID_4850114,Human_RBP_ID_7390270,Human_RBP_ID_8603964,Human_RBP_ID_9262294,Human_RBP_ID_9349975,Human_RBP_ID_9398278,Human_RBP_ID_15315396,Human_RBP_ID_17527576,Human_RBP_ID_18833511,Human_RBP_ID_25860523,Human_RBP_ID_27511838,Human_RBP_ID_27735367 Human_Splice_Rec_696724,Human_Splice_Rec_696725,Human_Splice_Rec_696754,Human_Splice_Rec_696755,Human_Splice_Rec_696772,Human_Splice_Rec_696773,Human_Splice_Rec_696804,Human_Splice_Rec_696805,Human_Splice_Rec_696813 RMVar_hsa_circ_7534,RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_26156,RMVar_hsa_circ_272810,RMVar_hsa_circ_56353,RMVar_hsa_circ_54952,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_234834,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_234835,RMVar_hsa_circ_269350,RMVar_hsa_circ_85314,RMVar_hsa_circ_370666,RMVar_hsa_circ_285035,RMVar_hsa_circ_127829,RMVar_hsa_circ_234838,RMVar_hsa_circ_234840,RMVar_hsa_circ_54836,RMVar_hsa_circ_234841,RMVar_hsa_circ_234839,RMVar_hsa_circ_234845,RMVar_hsa_circ_271745,RMVar_hsa_circ_354397,RMVar_hsa_circ_375775,RMVar_hsa_circ_289097,RMVar_hsa_circ_234847,RMVar_hsa_circ_80971,RMVar_hsa_circ_234846,RMVar_hsa_circ_35334,RMVar_hsa_circ_375808,RMVar_hsa_circ_346812,RMVar_hsa_circ_31470,RMVar_hsa_circ_234848 109735 RMVar_ID_109735 Human_SNP_ID_253244788 m1A Human chr5 - 138573837 138573837 138573837 TGTTCTAAATGTCTTACAGATCAGAAGCAATCAAGGGAGCAGTTGTTGGTATTGATTTGGGTACT TGTTCTAAATGTCTTACAGATCAGAAGCAATCCAGGGAGCAGTTGTTGGTATTGATTTGGGTACT T G HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138573708..138573901 26863196 MeRIP-seq:(Medium) rs1204302163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74199,Human_RBP_ID_632771,Human_RBP_ID_943007,Human_RBP_ID_1210831,Human_RBP_ID_1987878,Human_RBP_ID_3968211,Human_RBP_ID_4850139,Human_RBP_ID_5395714,Human_RBP_ID_7390324,Human_RBP_ID_9335727,Human_RBP_ID_9349697,Human_RBP_ID_17302363,Human_RBP_ID_18039779,Human_RBP_ID_18448142,Human_RBP_ID_22460208,Human_RBP_ID_22680763,Human_RBP_ID_24386562,Human_RBP_ID_27735380 Human_Splice_Rec_696712,Human_Splice_Rec_696713,Human_Splice_Rec_696744,Human_Splice_Rec_696745,Human_Splice_Rec_696792,Human_Splice_Rec_696793,Human_Splice_Rec_696826,Human_Splice_Rec_696827,Human_Splice_Rec_696840,Human_Splice_Rec_696841,Human_Splice_Rec_696846,Human_Splice_Rec_696847,Human_Splice_Rec_696854,Human_Splice_Rec_696855,Human_Splice_Rec_696862,Human_Splice_Rec_696863,Human_Splice_Rec_696868,Human_Splice_Rec_696869 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_234835,RMVar_hsa_circ_370666,RMVar_hsa_circ_234838,RMVar_hsa_circ_54836,RMVar_hsa_circ_354397,RMVar_hsa_circ_234847,RMVar_hsa_circ_80971,RMVar_hsa_circ_35334,RMVar_hsa_circ_346812,RMVar_hsa_circ_359269,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_234855,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234854,RMVar_hsa_circ_41346,RMVar_hsa_circ_341181 109736 RMVar_ID_109736 Human_SNP_ID_253244791 m1A Human chr5 - 138573847 138573847 138573847 GCTGTGACACTGTTCTAAATGTCTTACAGATCAGAAGCAATCAAGGGAGCAGTTGTTGGTATTGA GCTGTGACACTGTTCTAAATGTCTTACAGATCGGAAGCAATCAAGGGAGCAGTTGTTGGTATTGA T C HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:138573826..138573850 26863196 MeRIP-seq:(Medium) rs373312007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74199,Human_RBP_ID_632771,Human_RBP_ID_943007,Human_RBP_ID_1987878,Human_RBP_ID_3968211,Human_RBP_ID_5395714,Human_RBP_ID_9349697,Human_RBP_ID_17302363,Human_RBP_ID_22460208,Human_RBP_ID_22680763,Human_RBP_ID_24386562,Human_RBP_ID_27074641 Human_Splice_Rec_696712,Human_Splice_Rec_696713,Human_Splice_Rec_696744,Human_Splice_Rec_696745,Human_Splice_Rec_696792,Human_Splice_Rec_696793,Human_Splice_Rec_696826,Human_Splice_Rec_696827,Human_Splice_Rec_696840,Human_Splice_Rec_696841,Human_Splice_Rec_696846,Human_Splice_Rec_696847,Human_Splice_Rec_696854,Human_Splice_Rec_696855,Human_Splice_Rec_696862,Human_Splice_Rec_696863,Human_Splice_Rec_696868,Human_Splice_Rec_696869 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_234835,RMVar_hsa_circ_370666,RMVar_hsa_circ_234838,RMVar_hsa_circ_54836,RMVar_hsa_circ_354397,RMVar_hsa_circ_234847,RMVar_hsa_circ_80971,RMVar_hsa_circ_35334,RMVar_hsa_circ_346812,RMVar_hsa_circ_359269,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_234855,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234854,RMVar_hsa_circ_41346,RMVar_hsa_circ_341181 109737 RMVar_ID_109737 Human_SNP_ID_253244870 m1A Human chr5 + 138574029 138574029 138574029 CACAAATGTAGAAAACACTGCTTTGAAGTTTAATATGTATTCCCTCTCAAAGGAAATGATATTAT CACAAATGTAGAAAACACTGCTTTGAAGTTTAGTATGTATTCCCTCTCAAAGGAAATGATATTAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138574027..138574172 26863196 MeRIP-seq:(Medium) rs1442089315 Functional Loss SNV dbSNP153 33..33 33 - - - 109738 RMVar_ID_109738 Human_SNP_ID_253245324 m1A Human chr5 - 138575292 138575292 138575292 TCCGCCATGATAAGTGCCAGCCGAGCTGCAGCAGCCCGTCTCGTGGGCGCCGCAGCCTCCCGGGG TCCGCCATGATAAGTGCCAGCCGAGCTGCAGCGGCCCGTCTCGTGGGCGCCGCAGCCTCCCGGGG T C HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:138575160..138575300 26863196 MeRIP-seq:(Medium) rs1180851307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74200,Human_RBP_ID_632773,Human_RBP_ID_1210833,Human_RBP_ID_1645688,Human_RBP_ID_4811854,Human_RBP_ID_8884943,Human_RBP_ID_9335351,Human_RBP_ID_18448144,Human_RBP_ID_22099684,Human_RBP_ID_22458953,Human_RBP_ID_22534028,Human_RBP_ID_26350534,Human_RBP_ID_27074644,Human_RBP_ID_27331823 Human_Splice_Rec_696709,Human_Splice_Rec_696741,Human_Splice_Rec_696789,Human_Splice_Rec_696823,Human_Splice_Rec_696837,Human_Splice_Rec_696845,Human_Splice_Rec_696859 Human_miRNA_ID_2709656 RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363 109739 RMVar_ID_109739 Human_SNP_ID_253245362 m1A Human chr5 - 138575337 138575337 138575337 TTTGCCGTCGGAGCGCTTGTTTGCTGCCTCGTACTCCTCCATTTATCCGCCATGATAAGTGCCAG TTTGCCGTCGGAGCGCTTGTTTGCTGCCTCGTGCTCCTCCATTTATCCGCCATGATAAGTGCCAG T C HSPA9 Ensembl:ENSG00000113013 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:138575226..138575375 26863410 MeRIP-seq:(Medium) rs1173654589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74200,Human_RBP_ID_1319466,Human_RBP_ID_1390244,Human_RBP_ID_1645688,Human_RBP_ID_4811854,Human_RBP_ID_5426901,Human_RBP_ID_5449338,Human_RBP_ID_5476252,Human_RBP_ID_5508920,Human_RBP_ID_7390356,Human_RBP_ID_8603992,Human_RBP_ID_8884944,Human_RBP_ID_9170260,Human_RBP_ID_9335351,Human_RBP_ID_15315633,Human_RBP_ID_18039782,Human_RBP_ID_18448145,Human_RBP_ID_18833528,Human_RBP_ID_22099684,Human_RBP_ID_22460210,Human_RBP_ID_22534028,Human_RBP_ID_24085383,Human_RBP_ID_26350534,Human_RBP_ID_27074646,Human_RBP_ID_27331824,Human_RBP_ID_27511847 Human_Splice_Rec_696709,Human_Splice_Rec_696741,Human_Splice_Rec_696789,Human_Splice_Rec_696823,Human_Splice_Rec_696837,Human_Splice_Rec_696845,Human_Splice_Rec_696859 RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363 109740 RMVar_ID_109740 Human_SNP_ID_253245372 m1A Human chr5 + 138575348 138575348 138575348 CATGGCGGATAAATGGAGGAGTACGAGGCAGCAAACAAGCGCTCCGACGGCAAAGAGCTGCGCGA CATGGCGGATAAATGGAGGAGTACGAGGCAGCCAACAAGCGCTCCGACGGCAAAGAGCTGCGCGA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:138575326..138575400 26863196 MeRIP-seq:(Medium) rs760711400 Functional Loss SNV dbSNP153 33..33 33 - - - 109741 RMVar_ID_109741 Human_SNP_ID_253288438 m1A Human chr5 - 138753502 138753502 138753502 GCGAGGAGGGAGGTACGAAGTTACCTGCGGCTAGCTGGGCGAGCGCTAAATTCCAGAGGCCCGAA GCGAGGAGGGAGGTACGAAGTTACCTGCGGCTGGCTGGGCGAGCGCTAAATTCCAGAGGCCCGAA T C LOC105379194 RNACentral:URS0000A76FDA lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:138753451..138753574 26863196 MeRIP-seq:(Medium) rs1040012511 Functional Loss SNV dbSNP153 33..33 33 - - - 109742 RMVar_ID_109742 Human_SNP_ID_253288441 m1A Human chr5 + 138753509 138753509 138753509 CTCTGGAATTTAGCGCTCGCCCAGCTAGCCGCAGGTAACTTCGTACCTCCCTCCTCGCGGGCGCG CTCTGGAATTTAGCGCTCGCCCAGCTAGCCGCCGGTAACTTCGTACCTCCCTCCTCGCGGGCGCG A C CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr5:138753494..138753729;chr5:138753460..138753711 26863196,32194978 MeRIP-seq:(Medium) rs898367431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845996,Human_RBP_ID_8894124,Human_RBP_ID_9306635,Human_RBP_ID_18425014,Human_RBP_ID_19126341,Human_RBP_ID_26351367 Human_Splice_Rec_696901,Human_Splice_Rec_696907,Human_Splice_Rec_696943,Human_Splice_Rec_696975,Human_Splice_Rec_697009,Human_Splice_Rec_697015,Human_Splice_Rec_697017 109743 RMVar_ID_109743 Human_SNP_ID_253288442 m1A Human chr5 + 138753509 138753509 138753509 CTCTGGAATTTAGCGCTCGCCCAGCTAGCCGCAGGTAACTTCGTACCTCCCTCCTCGCGGGCGCG CTCTGGAATTTAGCGCTCGCCCAGCTAGCCGCGGGTAACTTCGTACCTCCCTCCTCGCGGGCGCG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr5:138753494..138753729;chr5:138753460..138753711 26863196,32194978 MeRIP-seq:(Medium) rs898367431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845996,Human_RBP_ID_8894124,Human_RBP_ID_9306635,Human_RBP_ID_18425014,Human_RBP_ID_19126341,Human_RBP_ID_26351367 Human_Splice_Rec_696901,Human_Splice_Rec_696907,Human_Splice_Rec_696943,Human_Splice_Rec_696975,Human_Splice_Rec_697009,Human_Splice_Rec_697015,Human_Splice_Rec_697017 109744 RMVar_ID_109744 Human_SNP_ID_253291943 m1A Human chr5 + 138766607 138766607 138766607 GGAAGGGGGTTAGTAGGGTGAGTGAGGTGTTTACTGAGGTACGGAGGAGAAAGAAAATGAGGCTA GGAAGGGGGTTAGTAGGGTGAGTGAGGTGTTTTCTGAGGTACGGAGGAGAAAGAAAATGAGGCTA A T CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138766601..138766681 26863196 MeRIP-seq:(Medium) rs976979126 Functional Loss SNV dbSNP153 33..33 33 - - - 109745 RMVar_ID_109745 Human_SNP_ID_253296620 m1A Human chr5 + 138781942 138781942 138781942 GTTTCTTATTTAGAAATGACTGCTGTCCATGCAGGCAACATAAACTTCAAGTGGGATCCTAAAAG GTTTCTTATTTAGAAATGACTGCTGTCCATGCGGGCAACATAAACTTCAAGTGGGATCCTAAAAG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:138781926..138781950 26863196 MeRIP-seq:(Medium) rs1449685929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73500,Human_RBP_ID_1645692,Human_RBP_ID_1987883,Human_RBP_ID_4845997,Human_RBP_ID_26351368 Human_Splice_Rec_696876,Human_Splice_Rec_696877,Human_Splice_Rec_696884,Human_Splice_Rec_696885,Human_Splice_Rec_696892,Human_Splice_Rec_696893,Human_Splice_Rec_696896,Human_Splice_Rec_696897,Human_Splice_Rec_696904,Human_Splice_Rec_696905,Human_Splice_Rec_696908,Human_Splice_Rec_696909,Human_Splice_Rec_696944,Human_Splice_Rec_696945,Human_Splice_Rec_696976,Human_Splice_Rec_696977,Human_Splice_Rec_697018,Human_Splice_Rec_697019,Human_Splice_Rec_697030,Human_Splice_Rec_697031,Human_Splice_Rec_697036,Human_Splice_Rec_697037,Human_Splice_Rec_697045 RMVar_hsa_circ_22103,RMVar_hsa_circ_351108,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_285964,RMVar_hsa_circ_297098,RMVar_hsa_circ_281108,RMVar_hsa_circ_234858,RMVar_hsa_circ_234859 109746 RMVar_ID_109746 Human_SNP_ID_253298676 m1A Human chr5 + 138790042 138790042 138790042 ATGAGGAAAAGTGGAGTTTTTGCAGGGAGATTAGTGTTAGCTGTGTGCAGGAAGGGTTAAAGTGA ATGAGGAAAAGTGGAGTTTTTGCAGGGAGATTGGTGTTAGCTGTGTGCAGGAAGGGTTAAAGTGA A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138790039..138790150 26863196 MeRIP-seq:(Medium) rs1169514063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7390501,Human_RBP_ID_15316176 RMVar_hsa_circ_22103,RMVar_hsa_circ_351108,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_285964,RMVar_hsa_circ_281108,RMVar_hsa_circ_61861,RMVar_hsa_circ_127244,RMVar_hsa_circ_234859,RMVar_hsa_circ_234861 109747 RMVar_ID_109747 Human_SNP_ID_253307633 m1A Human chr5 - 138824642 138824642 138824642 ATATCAGGTCCCTGTTGGCCTTATAGGCTGCGACATCAGGGTGCTGTAGGCATGCCTGGGATGCA ATATCAGGTCCCTGTTGGCCTTATAGGCTGCGGCATCAGGGTGCTGTAGGCATGCCTGGGATGCA T C RF00017-4932 RNACentral:URS000096C9DE SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138824592..138824733 26863196 MeRIP-seq:(Medium) rs992791147 Functional Loss SNV dbSNP153 33..33 33 - - - 109748 RMVar_ID_109748 Human_SNP_ID_253307685 m1A Human chr5 + 138824750 138824750 138824750 CCAGGCCACTGCCTCAGACGATGCCTCACAGCACCAGGGTGGAGGAGGAGGAGAACTGGCATATG CCAGGCCACTGCCTCAGACGATGCCTCACAGCGCCAGGGTGGAGGAGGAGGAGAACTGGCATATG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138824539..138827754 32194978 MeRIP-seq:(Medium) rs201055659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73512,Human_RBP_ID_632785,Human_RBP_ID_838530,Human_RBP_ID_946135,Human_RBP_ID_1987895,Human_RBP_ID_4811900,Human_RBP_ID_5610364,Human_RBP_ID_7390595,Human_RBP_ID_8894128,Human_RBP_ID_9306637,Human_RBP_ID_22459292,Human_RBP_ID_26351370 Human_Splice_Rec_696917,Human_Splice_Rec_696951,Human_Splice_Rec_696985,Human_Splice_Rec_697053,Human_Splice_Rec_697087,Human_Splice_Rec_697095 RMVar_hsa_circ_22103,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_285964,RMVar_hsa_circ_57022,RMVar_hsa_circ_61861,RMVar_hsa_circ_234859,RMVar_hsa_circ_281077,RMVar_hsa_circ_77477,RMVar_hsa_circ_234863,RMVar_hsa_circ_35282,RMVar_hsa_circ_234864,RMVar_hsa_circ_375894,RMVar_hsa_circ_348825,RMVar_hsa_circ_234868,RMVar_hsa_circ_234866,RMVar_hsa_circ_271679,RMVar_hsa_circ_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867 109749 RMVar_ID_109749 Human_SNP_ID_253307686 m1A Human chr5 + 138824750 138824750 138824750 CCAGGCCACTGCCTCAGACGATGCCTCACAGCACCAGGGTGGAGGAGGAGGAGAACTGGCATATG CCAGGCCACTGCCTCAGACGATGCCTCACAGCTCCAGGGTGGAGGAGGAGGAGAACTGGCATATG A T CTNNA1 Ensembl:ENSG00000044115 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138824539..138827754 32194978 MeRIP-seq:(Medium) rs201055659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73512,Human_RBP_ID_632785,Human_RBP_ID_838530,Human_RBP_ID_946135,Human_RBP_ID_1987895,Human_RBP_ID_4811900,Human_RBP_ID_5610364,Human_RBP_ID_7390595,Human_RBP_ID_8894128,Human_RBP_ID_9306637,Human_RBP_ID_22459292,Human_RBP_ID_26351370 Human_Splice_Rec_696917,Human_Splice_Rec_696951,Human_Splice_Rec_696985,Human_Splice_Rec_697053,Human_Splice_Rec_697087,Human_Splice_Rec_697095 RMVar_hsa_circ_22103,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_285964,RMVar_hsa_circ_57022,RMVar_hsa_circ_61861,RMVar_hsa_circ_234859,RMVar_hsa_circ_281077,RMVar_hsa_circ_77477,RMVar_hsa_circ_234863,RMVar_hsa_circ_35282,RMVar_hsa_circ_234864,RMVar_hsa_circ_375894,RMVar_hsa_circ_348825,RMVar_hsa_circ_234868,RMVar_hsa_circ_234866,RMVar_hsa_circ_271679,RMVar_hsa_circ_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867 109750 RMVar_ID_109750 Human_SNP_ID_253321753 m1A Human chr5 + 138882332 138882332 138882332 TATGTAGGTGAGAGAGAGCACGGCATGTCTGAAGAACAAAAATGTATGTGGGTGGGTCAGCATGG TATGTAGGTGAGAGAGAGCACGGCATGTCTGAGGAACAAAAATGTATGTGGGTGGGTCAGCATGG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:138882328..138882412 26863196 MeRIP-seq:(Medium) rs544531320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1108296,Human_RBP_ID_2898892,Human_RBP_ID_15316870 RMVar_hsa_circ_22103,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_61861,RMVar_hsa_circ_77477,RMVar_hsa_circ_35282,RMVar_hsa_circ_234864,RMVar_hsa_circ_348825,RMVar_hsa_circ_30105,RMVar_hsa_circ_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867,RMVar_hsa_circ_330821,RMVar_hsa_circ_31796,RMVar_hsa_circ_17698 109751 RMVar_ID_109751 Human_SNP_ID_253322576 m1A Human chr5 - 138886160 138886149 138886160 ATGAGCATTTTATTCATTTACAAAGAAACCTAATGATAGCCTATAGCCATTTGTGCTCATGTCAA ATGAGCATTTTATTCATTTACAAAGAAACCTA___________TAGCCATTTGTGCTCATGTCAA ATAGGCTATCAT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138886157..138886231 26863196 MeRIP-seq:(Medium) rs1419844928 Functional Loss DEL dbSNP153 33..43 33 - - - 109752 RMVar_ID_109752 Human_SNP_ID_253337149 m1A Human chr5 + 138944194 138944194 138944194 CCCAGGGCCAGAGCCCTTGCCCTGCCTGCCCCAGACTGGCCCTTCCAACTGCCCATCCCTGACTG CCCAGGGCCAGAGCCCTTGCCCTGCCTGCCCCGGACTGGCCCTTCCAACTGCCCATCCCTGACTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138944151..138944271 26863196 MeRIP-seq:(Medium) rs1265409886 Functional Loss SNV dbSNP153 33..33 33 - - - 109753 RMVar_ID_109753 Human_SNP_ID_253337532 m1A Human chr5 - 138945511 138945511 138945511 AAATGGCCGGGCATGTGTGGCCACAACAGGGCAGGCAGGTTTCAGACAGGAGGTGCCAGCGCCTG AAATGGCCGGGCATGTGTGGCCACAACAGGGCGGGCAGGTTTCAGACAGGAGGTGCCAGCGCCTG T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138945319..138945562 26863196 MeRIP-seq:(Medium) rs559118162 Functional Loss SNV dbSNP153 33..33 33 - - - 109754 RMVar_ID_109754 Human_SNP_ID_253354645 m1A Human chr5 - 139021241 139021241 139021241 TGCTTTCCTTTGGTGGTCTTCAAGTGGTGATCAATGGGCTGAACAGCACAGAGCCCCTCGTGAAG TGCTTTCCTTTGGTGGTCTTCAAGTGGTGATCGATGGGCTGAACAGCACAGAGCCCCTCGTGAAG T C SIL1 Ensembl:ENSG00000120725 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:139021191..139021291 32194978 MeRIP-seq:(Medium) rs921440617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4812030,Human_RBP_ID_18039874,Human_RBP_ID_19015122,Human_RBP_ID_22771762 Human_Splice_Rec_697322,Human_Splice_Rec_697323,Human_Splice_Rec_697342,Human_Splice_Rec_697343,Human_Splice_Rec_697368,Human_Splice_Rec_697369,Human_Splice_Rec_697382,Human_Splice_Rec_697383,Human_Splice_Rec_697386,Human_Splice_Rec_697387 RMVar_hsa_circ_7892,RMVar_hsa_circ_102128,RMVar_hsa_circ_234880,RMVar_hsa_circ_352131,RMVar_hsa_circ_371391,RMVar_hsa_circ_94164,RMVar_hsa_circ_234882,RMVar_hsa_circ_4400,RMVar_hsa_circ_234883 109755 RMVar_ID_109755 Human_SNP_ID_253354663 m1A Human chr5 + 139021291 139021291 139021291 CACCAAAGGAAAGCAGGTCCTGCGCATTGTCCATCTGCAACAGAGCCACTGCTTAGTACAGCATA CACCAAAGGAAAGCAGGTCCTGCGCATTGTCCCTCTGCAACAGAGCCACTGCTTAGTACAGCATA A C AC011405.1 Ensembl:ENSG00000249593 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139021240..139026848 32194978 MeRIP-seq:(Medium) rs1490321324 Functional Loss SNV dbSNP153 33..33 33 - - - 109756 RMVar_ID_109756 Human_SNP_ID_253417472 m1A Human chr5 - 139294365 139294365 139294365 AAAGAAACGCTGCTCAAACAAGCAGGCTCTTCAGAGTCTGCGAAATCCTCCATTTTGGGGGAACA AAAGAAACGCTGCTCAAACAAGCAGGCTCTTCGGAGTCTGCGAAATCCTCCATTTTGGGGGAACA T C RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:139294326..139294466 26863196 MeRIP-seq:(Medium) rs1042439969 Functional Loss SNV dbSNP153 33..33 33 - - - 109757 RMVar_ID_109757 Human_SNP_ID_253417473 m1A Human chr5 - 139294365 139294365 139294365 AAAGAAACGCTGCTCAAACAAGCAGGCTCTTCAGAGTCTGCGAAATCCTCCATTTTGGGGGAACA AAAGAAACGCTGCTCAAACAAGCAGGCTCTTCCGAGTCTGCGAAATCCTCCATTTTGGGGGAACA T G RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:139294326..139294466 26863196 MeRIP-seq:(Medium) rs1042439969 Functional Loss SNV dbSNP153 33..33 33 - - - 109758 RMVar_ID_109758 Human_SNP_ID_253421194 m1A Human chr5 + 139307657 139307657 139307657 TAGTGCACTGTCTTCTGCTAGTACTTCTTCCCATAATTTGCAGTCTATATTTAACATTGGAAGTA TAGTGCACTGTCTTCTGCTAGTACTTCTTCCCGTAATTTGCAGTCTATATTTAACATTGGAAGTA A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139307414..139307967 32194978 MeRIP-seq:(Medium) rs1186726385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_632917,Human_RBP_ID_1319534,Human_RBP_ID_1645841,Human_RBP_ID_1988129,Human_RBP_ID_2899802,Human_RBP_ID_3759371,Human_RBP_ID_7391827,Human_RBP_ID_8604374,Human_RBP_ID_8885038,Human_RBP_ID_15319426,Human_RBP_ID_17298253,Human_RBP_ID_17527626,Human_RBP_ID_18039962,Human_RBP_ID_18833729,Human_RBP_ID_27074788,Human_RBP_ID_27735469 Human_miRNA_ID_2087812,Human_miRNA_ID_2087813 RMVar_hsa_circ_234897,RMVar_hsa_circ_91210,RMVar_hsa_circ_116622,RMVar_hsa_circ_115834,RMVar_hsa_circ_234892,RMVar_hsa_circ_372248,RMVar_hsa_circ_126406,RMVar_hsa_circ_101392,RMVar_hsa_circ_109941,RMVar_hsa_circ_79033,RMVar_hsa_circ_85144,RMVar_hsa_circ_89228,RMVar_hsa_circ_234901,RMVar_hsa_circ_234903,RMVar_hsa_circ_234904,RMVar_hsa_circ_234902,RMVar_hsa_circ_234899,RMVar_hsa_circ_234900,RMVar_hsa_circ_234898,RMVar_hsa_circ_122270,RMVar_hsa_circ_234896,RMVar_hsa_circ_234912,RMVar_hsa_circ_66099,RMVar_hsa_circ_118135,RMVar_hsa_circ_302108,RMVar_hsa_circ_234914,RMVar_hsa_circ_114464,RMVar_hsa_circ_234915,RMVar_hsa_circ_62131,RMVar_hsa_circ_234916 109759 RMVar_ID_109759 Human_SNP_ID_253423576 m1A Human chr5 + 139316175 139316175 139316175 TCATTTCATCTTGGGGGACCAGCAGTTGGACCAAGAGGAAATCTGGGTAATTATATAAAATTCAT TCATTTCATCTTGGGGGACCAGCAGTTGGACCGAGAGGAAATCTGGGTAATTATATAAAATTCAT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139308265..139318989 32194978 MeRIP-seq:(Medium) rs375938101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284413,Human_RBP_ID_787295,Human_RBP_ID_1645927,Human_RBP_ID_1988205,Human_RBP_ID_7392125,Human_RBP_ID_8885066,Human_RBP_ID_9398295,Human_RBP_ID_18833796,Human_RBP_ID_19015125,Human_RBP_ID_19126360,Human_RBP_ID_23050425,Human_RBP_ID_26826591 Human_Splice_Rec_697484,Human_Splice_Rec_697485,Human_Splice_Rec_697512,Human_Splice_Rec_697522,Human_Splice_Rec_697536,Human_Splice_Rec_697537,Human_Splice_Rec_697572,Human_Splice_Rec_697573,Human_Splice_Rec_697606,Human_Splice_Rec_697607,Human_Splice_Rec_697640,Human_Splice_Rec_697641,Human_Splice_Rec_697674,Human_Splice_Rec_697675,Human_Splice_Rec_697774,Human_Splice_Rec_697775,Human_Splice_Rec_697784,Human_Splice_Rec_697785,Human_Splice_Rec_697798,Human_Splice_Rec_697799,Human_Splice_Rec_697806,Human_Splice_Rec_697807,Human_Splice_Rec_697816,Human_Splice_Rec_697817,Human_Splice_Rec_697844,Human_Splice_Rec_697845,Human_Splice_Rec_697876,Human_Splice_Rec_697877,Human_Splice_Rec_697904,Human_Splice_Rec_697905,Human_Splice_Rec_697912,Human_Splice_Rec_697913,Human_Splice_Rec_697922,Human_Splice_Rec_697923,Human_Splice_Rec_697950,Human_Splice_Rec_697951,Human_Splice_Rec_697978,Human_Splice_Rec_697979,Human_Splice_Rec_697985,Human_Splice_Rec_698012,Human_Splice_Rec_698013,Human_Splice_Rec_698028,Human_Splice_Rec_698029,Human_Splice_Rec_698050,Human_Splice_Rec_698051,Human_Splice_Rec_698053 Human_miRNA_ID_2033871,Human_miRNA_ID_2035175 RMVar_hsa_circ_234897,RMVar_hsa_circ_91210,RMVar_hsa_circ_116622,RMVar_hsa_circ_234892,RMVar_hsa_circ_126406,RMVar_hsa_circ_101392,RMVar_hsa_circ_109941,RMVar_hsa_circ_79033,RMVar_hsa_circ_85144,RMVar_hsa_circ_89228,RMVar_hsa_circ_234901,RMVar_hsa_circ_234902,RMVar_hsa_circ_234899,RMVar_hsa_circ_234900,RMVar_hsa_circ_234898,RMVar_hsa_circ_56035,RMVar_hsa_circ_122270,RMVar_hsa_circ_234896,RMVar_hsa_circ_234912,RMVar_hsa_circ_66099,RMVar_hsa_circ_114464,RMVar_hsa_circ_62131,RMVar_hsa_circ_234916,RMVar_hsa_circ_317505,RMVar_hsa_circ_333012,RMVar_hsa_circ_335093,RMVar_hsa_circ_332858,RMVar_hsa_circ_80966,RMVar_hsa_circ_55566,RMVar_hsa_circ_27012,RMVar_hsa_circ_234918,RMVar_hsa_circ_43369,RMVar_hsa_circ_234919,RMVar_hsa_circ_234917,RMVar_hsa_circ_72323,RMVar_hsa_circ_288584,RMVar_hsa_circ_361395,RMVar_hsa_circ_59656 109760 RMVar_ID_109760 Human_SNP_ID_253426781 m1A Human chr5 + 139325504 139325504 139325504 CGAAGCAGCGTTGGAAAATGGAATTAAAAATGAGGAAAACACAGAACCAGGTGCTGAATCTTCTG CGAAGCAGCGTTGGAAAATGGAATTAAAAATGGGGAAAACACAGAACCAGGTGCTGAATCTTCTG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:139325453..139325587 26863196 MeRIP-seq:(Medium) rs538917496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_73090,Human_RBP_ID_284414,Human_RBP_ID_1210922,Human_RBP_ID_1645980,Human_RBP_ID_1988238,Human_RBP_ID_2956831,Human_RBP_ID_3759434,Human_RBP_ID_7392241,Human_RBP_ID_8267376,Human_RBP_ID_8604437,Human_RBP_ID_8885089,Human_RBP_ID_9170452,Human_RBP_ID_9398316,Human_RBP_ID_15320318,Human_RBP_ID_17298275,Human_RBP_ID_17411844,Human_RBP_ID_17527643,Human_RBP_ID_18183076,Human_RBP_ID_18413715,Human_RBP_ID_18537766,Human_RBP_ID_18833835,Human_RBP_ID_19124738,Human_RBP_ID_24085906,Human_RBP_ID_24548023,Human_RBP_ID_26351389,Human_RBP_ID_27074845,Human_RBP_ID_27735508,Human_RBP_ID_27826838 Human_Splice_Rec_697500,Human_Splice_Rec_697552,Human_Splice_Rec_697588,Human_Splice_Rec_697832,Human_Splice_Rec_697860,Human_Splice_Rec_697892,Human_Splice_Rec_697938,Human_Splice_Rec_697966,Human_Splice_Rec_698044 Human_miRNA_ID_2998039 Clinvar_Rec_732 RMVar_hsa_circ_234897,RMVar_hsa_circ_101392,RMVar_hsa_circ_85144,RMVar_hsa_circ_56035,RMVar_hsa_circ_234896,RMVar_hsa_circ_62131,RMVar_hsa_circ_234919,RMVar_hsa_circ_72323,RMVar_hsa_circ_288584,RMVar_hsa_circ_61079,RMVar_hsa_circ_33277,RMVar_hsa_circ_320086,RMVar_hsa_circ_68813,RMVar_hsa_circ_350313 109761 RMVar_ID_109761 Human_SNP_ID_253427935 m1A Human chr5 + 139329479 139329475 139329479 TAATGTTAACCTTTTTTAAATACAATACTGATAGTTAGAAGAAAACTATTGTACTCTTTTGTTTT TAATGTTAACCTTTTTTAAATACAATACT____GTTAGAAGAAAACTATTGTACTCTTTTGTTTT TGATA T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139329428..139329586 32194978 MeRIP-seq:(Medium) rs1481395643 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_633010,Human_RBP_ID_1988266,Human_RBP_ID_7392360,Human_RBP_ID_9170472,Human_RBP_ID_18353928,Human_RBP_ID_24085950 Human_miRNA_ID_1032277,Human_miRNA_ID_1032278,Human_miRNA_ID_1506100,Human_miRNA_ID_1506101,Human_miRNA_ID_1775995,Human_miRNA_ID_1775996 RMVar_hsa_circ_85144,RMVar_hsa_circ_234896 109762 RMVar_ID_109762 Human_SNP_ID_253427939 m1A Human chr5 + 139329479 139329479 139329479 TAATGTTAACCTTTTTTAAATACAATACTGATAGTTAGAAGAAAACTATTGTACTCTTTTGTTTT TAATGTTAACCTTTTTTAAATACAATACTGATGGTTAGAAGAAAACTATTGTACTCTTTTGTTTT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding 3'UTR,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139329428..139329586 32194978 MeRIP-seq:(Medium) rs1435794737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633010,Human_RBP_ID_1988266,Human_RBP_ID_7392360,Human_RBP_ID_9170472,Human_RBP_ID_18353928,Human_RBP_ID_24085950 Human_miRNA_ID_1032277,Human_miRNA_ID_1032278,Human_miRNA_ID_1506100,Human_miRNA_ID_1506101,Human_miRNA_ID_1775995,Human_miRNA_ID_1775996 RMVar_hsa_circ_85144,RMVar_hsa_circ_234896 109763 RMVar_ID_109763 Human_SNP_ID_253437773 m1A Human chr5 + 139363880 139363880 139363880 GGTCATTCTCATGAAGATGACAATCCATTTGCAGAGTACATGTGGATGGAAAATGAAGAAGAATT GGTCATTCTCATGAAGATGACAATCCATTTGCGGAGTACATGTGGATGGAAAATGAAGAAGAATT A G PAIP2 Ensembl:ENSG00000120727 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139363830..139363979 32194978 MeRIP-seq:(Medium) rs201030798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633074,Human_RBP_ID_1646076,Human_RBP_ID_1988314,Human_RBP_ID_4812292,Human_RBP_ID_9398322,Human_RBP_ID_17662584,Human_RBP_ID_24548128,Human_RBP_ID_26351397,Human_RBP_ID_27825887 Human_Splice_Rec_698085,Human_Splice_Rec_698089,Human_Splice_Rec_698095,Human_Splice_Rec_698103,Human_Splice_Rec_698111,Human_Splice_Rec_698117 RMVar_hsa_circ_1043,RMVar_hsa_circ_272539,RMVar_hsa_circ_234925 109764 RMVar_ID_109764 Human_SNP_ID_253437777 m1A Human chr5 - 139363901 139363901 139363901 AAAAAACTAACTTGTCTGTTGAATTCTTCTTCATTTTCCATCCACATGTACTCTGCAAATGGATT AAAAAACTAACTTGTCTGTTGAATTCTTCTTCGTTTTCCATCCACATGTACTCTGCAAATGGATT T C RF00017-4525 RNACentral:URS00009368C0 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139363851..139363925 26863196 MeRIP-seq:(Medium) rs1196564723 Functional Loss SNV dbSNP153 33..33 33 - - - 109765 RMVar_ID_109765 Human_SNP_ID_253448948 m1A Human chr5 + 139404021 139404021 139404021 GTCCCGCAGTTGATCTAAAGCGAGACACACAGATCCTGACCCCGCCTTCGACCACCCGAGGGGCG GTCCCGCAGTTGATCTAAAGCGAGACACACAGGTCCTGACCCCGCCTTCGACCACCCGAGGGGCG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:139403924..139404056 26863196 MeRIP-seq:(Medium) rs1397902673 Functional Loss SNV dbSNP153 33..33 33 - - - 109766 RMVar_ID_109766 Human_SNP_ID_253448950 m1A Human chr5 - 139404025 139404025 139404025 GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCAGGATCTGTGTGTCTCGCTTTAGATCAACTGCG GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCTGGATCTGTGTGTCTCGCTTTAGATCAACTGCG T A SPATA24 Ensembl:ENSG00000170469 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139402645..139404055 26863196 MeRIP-seq:(Medium) rs886829626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4812394,Human_RBP_ID_18425177 Human_Splice_Rec_698241,Human_Splice_Rec_698251,Human_Splice_Rec_698269,Human_Splice_Rec_698277,Human_Splice_Rec_698281,Human_Splice_Rec_698287 109767 RMVar_ID_109767 Human_SNP_ID_253448951 m1A Human chr5 - 139404025 139404025 139404025 GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCAGGATCTGTGTGTCTCGCTTTAGATCAACTGCG GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCGGGATCTGTGTGTCTCGCTTTAGATCAACTGCG T C SPATA24 Ensembl:ENSG00000170469 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139402645..139404055 26863196 MeRIP-seq:(Medium) rs886829626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4812394,Human_RBP_ID_18425177 Human_Splice_Rec_698241,Human_Splice_Rec_698251,Human_Splice_Rec_698269,Human_Splice_Rec_698277,Human_Splice_Rec_698281,Human_Splice_Rec_698287 109768 RMVar_ID_109768 Human_SNP_ID_253448952 m1A Human chr5 - 139404025 139404025 139404025 GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCAGGATCTGTGTGTCTCGCTTTAGATCAACTGCG GCGACGCCCCTCGGGTGGTCGAAGGCGGGGTCCGGATCTGTGTGTCTCGCTTTAGATCAACTGCG T G SPATA24 Ensembl:ENSG00000170469 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139402645..139404055 26863196 MeRIP-seq:(Medium) rs886829626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4812394,Human_RBP_ID_18425177 Human_Splice_Rec_698241,Human_Splice_Rec_698251,Human_Splice_Rec_698269,Human_Splice_Rec_698277,Human_Splice_Rec_698281,Human_Splice_Rec_698287 109769 RMVar_ID_109769 Human_SNP_ID_253456765 m1A Human chr5 + 139439457 139439457 139439457 GCTGCCCAGAGTCGCCGCCATATCGGTTCCCAATCAGCAGGTCCGCCGAGCCTCCCCCGTGCCCG GCTGCCCAGAGTCGCCGCCATATCGGTTCCCAGTCAGCAGGTCCGCCGAGCCTCCCCCGTGCCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139439352..139439479 26863196 MeRIP-seq:(Medium) rs148652357 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 109770 RMVar_ID_109770 Human_SNP_ID_253488069 m1A Human chr5 + 139561524 139561524 139561524 CGGTTTAGGAGGCGGCGCTGATCCTGGGAGGAAGAGGCAGCTACGGCGGCGGCGGCGGTGGCGGC CGGTTTAGGAGGCGGCGCTGATCCTGGGAGGACGAGGCAGCTACGGCGGCGGCGGCGGTGGCGGC A C UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139561340..139562036 26863196 MeRIP-seq:(Medium) rs1479595604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75197,Human_RBP_ID_4846015,Human_RBP_ID_5326864,Human_RBP_ID_7392916,Human_RBP_ID_17662932,Human_RBP_ID_22099689,Human_RBP_ID_22534031,Human_RBP_ID_23120200 Human_miRNA_ID_2240720 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 109771 RMVar_ID_109771 Human_SNP_ID_253488070 m1A Human chr5 + 139561524 139561524 139561524 CGGTTTAGGAGGCGGCGCTGATCCTGGGAGGAAGAGGCAGCTACGGCGGCGGCGGCGGTGGCGGC CGGTTTAGGAGGCGGCGCTGATCCTGGGAGGAGGAGGCAGCTACGGCGGCGGCGGCGGTGGCGGC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139561340..139562036 26863196 MeRIP-seq:(Medium) rs1479595604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75197,Human_RBP_ID_4846015,Human_RBP_ID_5326864,Human_RBP_ID_7392916,Human_RBP_ID_17662932,Human_RBP_ID_22099689,Human_RBP_ID_22534031,Human_RBP_ID_23120200 Human_miRNA_ID_2240720 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 109772 RMVar_ID_109772 Human_SNP_ID_253488098 m1A Human chr5 - 139561572 139561572 139561572 CGGTCACCGCATCACCCGGCGGCGGCCCCTTTATTCGCCGCCGCCCTAGCCGCCACCGCCGCCGC CGGTCACCGCATCACCCGGCGGCGGCCCCTTTCTTCGCCGCCGCCCTAGCCGCCACCGCCGCCGC T G RF00017-4685 RNACentral:URS0000985E23 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:139561526..139561575 26863196 MeRIP-seq:(Medium) rs1241479798 Functional Loss SNV dbSNP153 33..33 33 - - - 109773 RMVar_ID_109773 Human_SNP_ID_253488142 m1A Human chr5 + 139561679 139561679 139561679 CGTCCCGCCGGACCCGCTTTCCTCAACTCTCCATCTTCTCCTGCCGACCGAGATCGCCGAGGCGG CGTCCCGCCGGACCCGCTTTCCTCAACTCTCCGTCTTCTCCTGCCGACCGAGATCGCCGAGGCGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:139561601..139561750 32194978 MeRIP-seq:(Medium) rs892966738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633134,Human_RBP_ID_4846018,Human_RBP_ID_5426918,Human_RBP_ID_5449360,Human_RBP_ID_5476271,Human_RBP_ID_5508942,Human_RBP_ID_7392917,Human_RBP_ID_8132827,Human_RBP_ID_8604602,Human_RBP_ID_9170531,Human_RBP_ID_9305000,Human_RBP_ID_9335359,Human_RBP_ID_15321914,Human_RBP_ID_17298324,Human_RBP_ID_18040173,Human_RBP_ID_18210428,Human_RBP_ID_18833951,Human_RBP_ID_18956147,Human_RBP_ID_23292576,Human_RBP_ID_25862578,Human_RBP_ID_26750973,Human_RBP_ID_27331970,Human_RBP_ID_27511964,Human_RBP_ID_27567238 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 109774 RMVar_ID_109774 Human_SNP_ID_253510094 m1A Human chr5 + 139648382 139648382 139648382 GCGGCGGCAGAGGCGGCTGAGCCTGAGCGGGGATGTAGAGGCGGCGGCAGCAGAGGCGGCACTGG GCGGCGGCAGAGGCGGCTGAGCCTGAGCGGGGTTGTAGAGGCGGCGGCAGCAGAGGCGGCACTGG A T CXXC5 Ensembl:ENSG00000171604 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:139648305..139651001 26863196 MeRIP-seq:(Medium) rs1295380931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846019,Human_RBP_ID_8943894,Human_RBP_ID_9306661,Human_RBP_ID_9335732,Human_RBP_ID_18425187 109775 RMVar_ID_109775 Human_SNP_ID_253510096 m1A Human chr5 - 139648383 139648383 139648383 GCCAGTGCCGCCTCTGCTGCCGCCGCCTCTACATCCCCGCTCAGGCTCAGCCGCCTCTGCCGCCG GCCAGTGCCGCCTCTGCTGCCGCCGCCTCTACGTCCCCGCTCAGGCTCAGCCGCCTCTGCCGCCG T C RF00017-4497 RNACentral:URS000098F9B6 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:139648289..139648857;chr5:139648287..139648676 26863196 MeRIP-seq:(Medium) rs970299966 Functional Loss SNV dbSNP153 33..33 33 - - - 109776 RMVar_ID_109776 Human_SNP_ID_253510097 m1A Human chr5 - 139648383 139648383 139648383 GCCAGTGCCGCCTCTGCTGCCGCCGCCTCTACATCCCCGCTCAGGCTCAGCCGCCTCTGCCGCCG GCCAGTGCCGCCTCTGCTGCCGCCGCCTCTACCTCCCCGCTCAGGCTCAGCCGCCTCTGCCGCCG T G RF00017-4497 RNACentral:URS000098F9B6 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:139648289..139648857;chr5:139648287..139648676 26863196 MeRIP-seq:(Medium) rs970299966 Functional Loss SNV dbSNP153 33..33 33 - - - 109777 RMVar_ID_109777 Human_SNP_ID_253510175 m1A Human chr5 - 139648579 139648579 139648579 AAAAAACAACAAAAAGCAACTAATCACCCCCGAGCTGAGCGCGGCTCGCGGGCGGAGGGCTCAGC AAAAAACAACAAAAAGCAACTAATCACCCCCGGGCTGAGCGCGGCTCGCGGGCGGAGGGCTCAGC T C RF00017-4497 RNACentral:URS000098F9B6 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:139648443..139648619 26863196 MeRIP-seq:(Medium) rs1034791985 Functional Loss SNV dbSNP153 33..33 33 - - - 109778 RMVar_ID_109778 Human_SNP_ID_253561114 m1A Human chr5 + 139849878 139849878 139849878 GGGTCTCTCCTCCTTCACTCTATGCAGTTCCCAGAGCAATCTTGTAAAGTCACAGCTCTGCTGAA GGGTCTCTCCTCCTTCACTCTATGCAGTTCCCTGAGCAATCTTGTAAAGTCACAGCTCTGCTGAA A T AC008667.2 Ensembl:ENSG00000250692 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139849863..139850172 26863196 MeRIP-seq:(Medium) rs948830122 Functional Loss SNV dbSNP153 33..33 33 - - - 109779 RMVar_ID_109779 Human_SNP_ID_253573086 m1A Human chr5 - 139904409 139904409 139904409 AGCGGAGAGCTGAGGCCGTCCCACCGCCTGGGACCCCGTGCAGAATGTCGGAGTCCAGGAGGAGG AGCGGAGAGCTGAGGCCGTCCCACCGCCTGGGGCCCCGTGCAGAATGTCGGAGTCCAGGAGGAGG T C NRG2 Ensembl:ENSG00000158458 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:139904360..139904456 26863196 MeRIP-seq:(Medium) rs532650058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1319582 RMVar_hsa_circ_119485,RMVar_hsa_circ_234959 109780 RMVar_ID_109780 Human_SNP_ID_253616796 m1A Human chr5 + 140107935 140107935 140107935 TGAGTGAGCGGGAGAAGCAGGGTGTGAGCCGGACTTGCCCATGGGAGGGAGAGCGAGCGAGAGCC TGAGTGAGCGGGAGAAGCAGGGTGTGAGCCGGCCTTGCCCATGGGAGGGAGAGCGAGCGAGAGCC A C PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:140107800..140108494;chr5:140107817..140108542;chr5:140107808..140112945 26863196 MeRIP-seq:(Medium) rs897845890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4847198,Human_RBP_ID_5449369,Human_RBP_ID_5508948,Human_RBP_ID_24554390,Human_RBP_ID_26791949 109781 RMVar_ID_109781 Human_SNP_ID_253616797 m1A Human chr5 + 140107935 140107935 140107935 TGAGTGAGCGGGAGAAGCAGGGTGTGAGCCGGACTTGCCCATGGGAGGGAGAGCGAGCGAGAGCC TGAGTGAGCGGGAGAAGCAGGGTGTGAGCCGGGCTTGCCCATGGGAGGGAGAGCGAGCGAGAGCC A G PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:140107800..140108494;chr5:140107817..140108542;chr5:140107808..140112945 26863196 MeRIP-seq:(Medium) rs897845890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4847198,Human_RBP_ID_5449369,Human_RBP_ID_5508948,Human_RBP_ID_24554390,Human_RBP_ID_26791949 109782 RMVar_ID_109782 Human_SNP_ID_253616968 m1A Human chr5 - 140108298 140108298 140108298 TCTGCAATGGTACTATAATTATTCCTGGGCTGAGAGAGCAAGTAAAGGGGACGGGGCGAGCGTCA TCTGCAATGGTACTATAATTATTCCTGGGCTGCGAGAGCAAGTAAAGGGGACGGGGCGAGCGTCA T G MALINC1 Ensembl:ENSG00000245146 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:140108210..140108297 26863410 MeRIP-seq:(Medium) rs1222923334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5615766 109783 RMVar_ID_109783 Human_SNP_ID_253618670 m1A Human chr5 + 140114125 140114116 140114125 GCCGGGGAGGGAAAGCAGCGGCGGCTGAGGCGACTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGC GCCGGGGAGGGAAAGCAGCGGCGG_________CTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGC GCTGAGGCGA G PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:140114076..140114265 26863196 MeRIP-seq:(Medium) rs1386467592 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_3783398,Human_RBP_ID_4845394,Human_RBP_ID_5242304,Human_RBP_ID_18501845,Human_RBP_ID_22727366,Human_RBP_ID_24554394,Human_RBP_ID_26792161 Human_Splice_Rec_699034,Human_Splice_Rec_699036,Human_Splice_Rec_699038 109784 RMVar_ID_109784 Human_SNP_ID_253618674 m1A Human chr5 + 140114125 140114125 140114125 GCCGGGGAGGGAAAGCAGCGGCGGCTGAGGCGACTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGC GCCGGGGAGGGAAAGCAGCGGCGGCTGAGGCGGCTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGC A G PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:140114076..140114265 26863196 MeRIP-seq:(Medium) rs1244613218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3783398,Human_RBP_ID_4845394,Human_RBP_ID_5242304,Human_RBP_ID_18501845,Human_RBP_ID_22727366,Human_RBP_ID_24554394,Human_RBP_ID_26792161 Human_Splice_Rec_699034,Human_Splice_Rec_699036,Human_Splice_Rec_699038 109785 RMVar_ID_109785 Human_SNP_ID_253618683 m1A Human chr5 + 140114148 140114136 140114148 GCTGAGGCGACTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGCGGCGCGGCAGCGGAGCGCAGCAT GCTGAGGCGACTGAGGCGGCG____________GGCGGCGGCGGCGCGGCAGCGGAGCGCAGCAT GGGCGGAGCGGCA G PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:140114026..140114401;chr5:140114026..140115373;chr5:140113188..140114881 26863196 MeRIP-seq:(Medium) rs1031890592 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_12771,Human_RBP_ID_788973,Human_RBP_ID_3782899,Human_RBP_ID_4845394,Human_RBP_ID_5242304,Human_RBP_ID_9436588,Human_RBP_ID_18501845,Human_RBP_ID_22727366,Human_RBP_ID_24554394 109786 RMVar_ID_109786 Human_SNP_ID_253618687 m1A Human chr5 + 140114142 140114142 140114142 GCGGCGGCTGAGGCGACTGAGGCGGCGGGCGGAGCGGCAGGCGGCGGCGGCGCGGCAGCGGAGCG GCGGCGGCTGAGGCGACTGAGGCGGCGGGCGGCGCGGCAGGCGGCGGCGGCGCGGCAGCGGAGCG A C PURA Ensembl:ENSG00000185129 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140113998..140114860 26863196 MeRIP-seq:(Medium) rs1291700288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12771,Human_RBP_ID_3782899,Human_RBP_ID_4845394,Human_RBP_ID_5242304,Human_RBP_ID_18501845,Human_RBP_ID_22727366,Human_RBP_ID_24554394 109787 RMVar_ID_109787 Human_SNP_ID_253618707 m1A Human chr5 + 140114210 140114210 140114210 CATCATGGCGGACCGAGACAGCGGCAGCGAGCAGGGTGGTGCGGCGCTGGGTTCGGGCGGCTCCC CATCATGGCGGACCGAGACAGCGGCAGCGAGCCGGGTGGTGCGGCGCTGGGTTCGGGCGGCTCCC A C PURA Ensembl:ENSG00000185129 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:140114117..140114313 26863410 MeRIP-seq:(Medium) rs1269489196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4812674,Human_RBP_ID_27511998 109788 RMVar_ID_109788 Human_SNP_ID_253618740 m1A Human chr5 - 140114286 140114277 140114286 CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCCACCACCGCCCCCGCCGGAGCCTGAGCCCGAGCC CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCC_________CCCGCCGGAGCCTGAGCCCGAGCC GGGCGGTGGT G MALINC1 RNACentral:URS0000D58F53 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:140114076..140114327 26863196 MeRIP-seq:(Medium) rs1260462826 Functional Loss DEL dbSNP153 33..41 33 - - - 109789 RMVar_ID_109789 Human_SNP_ID_253618741 m1A Human chr5 + 140114308 140114281 140114308 GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCAGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGGGCG___________________________GTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGTGGTGGCGGCGGGGGCGGCGGCGGCA G PURA Ensembl:ENSG00000185129 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:140114126..140114373 26863410 MeRIP-seq:(Medium) rs1433370088 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_214396,Human_RBP_ID_250980,Human_RBP_ID_3783399,Human_RBP_ID_5242441,Human_RBP_ID_8730244,Human_RBP_ID_9335377,Human_RBP_ID_22099710,Human_RBP_ID_22727492,Human_RBP_ID_23258903,Human_RBP_ID_26792162,Human_RBP_ID_27075005 Clinvar_Rec_733 109790 RMVar_ID_109790 Human_SNP_ID_253618742 m1A Human chr5 - 140114283 140114283 140114283 CCGCCACTGCCGCCGCCGCCCCCGCCGCCACCACCGCCCCCGCCGGAGCCTGAGCCCGAGCCGGG CCGCCACTGCCGCCGCCGCCCCCGCCGCCACCCCCGCCCCCGCCGGAGCCTGAGCCCGAGCCGGG T G MALINC1 RNACentral:URS0000D58F53 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:140114094..140114296 26863196 MeRIP-seq:(Medium) rs1446546980 Functional Loss SNV dbSNP153 33..33 33 - - - 109791 RMVar_ID_109791 Human_SNP_ID_253618743 m1A Human chr5 + 140114308 140114284 140114308 GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCAGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGGGCGGTG________________________GTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGTGGCGGCGGGGGCGGCGGCGGCA G PURA Ensembl:ENSG00000185129 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:140114126..140114373 26863410 MeRIP-seq:(Medium) rs751351711 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_214396,Human_RBP_ID_250980,Human_RBP_ID_3783399,Human_RBP_ID_5242441,Human_RBP_ID_8730244,Human_RBP_ID_9335377,Human_RBP_ID_22099710,Human_RBP_ID_22727492,Human_RBP_ID_23258903,Human_RBP_ID_26792162,Human_RBP_ID_27075005 109792 RMVar_ID_109792 Human_SNP_ID_253618748 m1A Human chr5 - 140114286 140114286 140114286 CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCCACCACCGCCCCCGCCGGAGCCTGAGCCCGAGCC CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCCGCCACCGCCCCCGCCGGAGCCTGAGCCCGAGCC T C MALINC1 RNACentral:URS0000D58F53 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:140114076..140114327 26863196 MeRIP-seq:(Medium) rs1282359377 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_734 109793 RMVar_ID_109793 Human_SNP_ID_253618749 m1A Human chr5 - 140114286 140114286 140114286 CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCCACCACCGCCCCCGCCGGAGCCTGAGCCCGAGCC CCGCCGCCACTGCCGCCGCCGCCCCCGCCGCCCCCACCGCCCCCGCCGGAGCCTGAGCCCGAGCC T G MALINC1 RNACentral:URS0000D58F53 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:140114076..140114327 26863196 MeRIP-seq:(Medium) rs1282359377 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_734 109794 RMVar_ID_109794 Human_SNP_ID_253618770 m1A Human chr5 + 140114308 140114308 140114308 GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCAGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG A G PURA Ensembl:ENSG00000185129 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:140114126..140114373 26863410 MeRIP-seq:(Medium) rs1335796595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214396,Human_RBP_ID_250980,Human_RBP_ID_3783399,Human_RBP_ID_5242441,Human_RBP_ID_8730244,Human_RBP_ID_9335377,Human_RBP_ID_22099710,Human_RBP_ID_22727492,Human_RBP_ID_23258903,Human_RBP_ID_26792162,Human_RBP_ID_27075005 109795 RMVar_ID_109795 Human_SNP_ID_253618979 m1A Human chr5 - 140114786 140114786 140114786 CCTCCACTCCGTAGTCGTCGATGAGCTTGGCCAGAGCGTCACGGAACTCGATGAGCCCCTGCGCG CCTCCACTCCGTAGTCGTCGATGAGCTTGGCCGGAGCGTCACGGAACTCGATGAGCCCCTGCGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140114735..140114873 26863196 MeRIP-seq:(Medium) rs1561793336 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_735 109796 RMVar_ID_109796 Human_SNP_ID_253619060 m1A Human chr5 - 140115023 140115023 140115023 AGGCAGCCCGCTTCTCCCTCTGCTTCTCTTGAATCTTCTTCATCTCCTCCGAGTACTTGCAGAAG AGGCAGCCCGCTTCTCCCTCTGCTTCTCTTGAGTCTTCTTCATCTCCTCCGAGTACTTGCAGAAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:140114972..140115323 26863196 MeRIP-seq:(Medium) rs765132127 Functional Loss SNV dbSNP153 33..33 33 - - - 109797 RMVar_ID_109797 Human_SNP_ID_253629891 m1A Human chr5 + 140165459 140165459 140165459 TCAGGGTCATGGGTGATATATTTGGGGAGTGTACAGGGAAAGAGGAGTAGTAGGCATTAGGGACA TCAGGGTCATGGGTGATATATTTGGGGAGTGTGCAGGGAAAGAGGAGTAGTAGGCATTAGGGACA A G AC011379.2 Ensembl:ENSG00000254363 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140165436..140165583 26863196 MeRIP-seq:(Medium) rs995195784 Functional Loss SNV dbSNP153 33..33 33 - - - 109798 RMVar_ID_109798 Human_SNP_ID_253632014 m1A Human chr5 - 140175287 140175287 140175287 CCAGCTGGGTCGGGCCAGGTCCGCTGCACCTCACCTCTCCTCTCCACGAACCGACTGGATAACGG CCAGCTGGGTCGGGCCAGGTCCGCTGCACCTCGCCTCTCCTCTCCACGAACCGACTGGATAACGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:140175187..140194525 26863410 MeRIP-seq:(Medium) rs1443320198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5426923 109799 RMVar_ID_109799 Human_SNP_ID_253636111 m1A Human chr5 - 140194610 140194610 140194610 AGGAGGCTCCTGAGGTCCACCCTGCCAGCCGTACTGTGGGTATCCTTGGTAGGGGTACCCTTGAG AGGAGGCTCCTGAGGTCCACCCTGCCAGCCGTGCTGTGGGTATCCTTGGTAGGGGTACCCTTGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140175237..140194675 32194978 MeRIP-seq:(Medium) rs753559685 Functional Loss SNV dbSNP153 33..33 33 - - - 109800 RMVar_ID_109800 Human_SNP_ID_253645923 m1A Human chr5 - 140243346 140243346 140243346 GAGAGCCGTCCAGCAGGCTGTGAGGCAGGTGGATGGTCCTAGCTCATCTCTTCTTTGGTCTTCTA GAGAGCCGTCCAGCAGGCTGTGAGGCAGGTGGGTGGTCCTAGCTCATCTCTTCTTTGGTCTTCTA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:140194595..140243347 26863410 MeRIP-seq:(Medium) rs1243848844 Functional Loss SNV dbSNP153 33..33 33 - - - 109801 RMVar_ID_109801 Human_SNP_ID_253646521 m1A Human chr5 + 140245550 140245550 140245550 CATCCCCCAAGAAAGGAAGGGCTCTGATGCAGAGGGAGCAGGAGCTGAGGTGGAGACGGCCACTG CATCCCCCAAGAAAGGAAGGGCTCTGATGCAGGGGGAGCAGGAGCTGAGGTGGAGACGGCCACTG A G CYSTM1 Ensembl:ENSG00000120306 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140245501..140246019 32194978 MeRIP-seq:(Medium) rs968654991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95577,RMVar_hsa_circ_234969 109802 RMVar_ID_109802 Human_SNP_ID_253648547 m1A Human chr5 - 140254428 140254428 140254428 GTCCGGTGGCTAAGCATGATGCCATGAACTTCAAGGACCAGGGTTTATGAAGGATAAAGGAGGGG GTCCGGTGGCTAAGCATGATGCCATGAACTTCCAGGACCAGGGTTTATGAAGGATAAAGGAGGGG T G PFDN1 Ensembl:ENSG00000113068 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140254425..140254664 26863196 MeRIP-seq:(Medium) rs1278975234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15324451 109803 RMVar_ID_109803 Human_SNP_ID_253648846 m1A Human chr5 + 140256009 140256009 140256009 TCTCTATGGGTGCTTCTCTGTCATCTTACTCAACCTCTCAACAGTGTTCAACACAGTTCTTGGAA TCTCTATGGGTGCTTCTCTGTCATCTTACTCAGCCTCTCAACAGTGTTCAACACAGTTCTTGGAA A G CYSTM1 Ensembl:ENSG00000120306 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140256008..140256149 26863196 MeRIP-seq:(Medium) rs949331026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95577,RMVar_hsa_circ_234969 109804 RMVar_ID_109804 Human_SNP_ID_253683165 m1A Human chr5 + 140402132 140402132 140402132 AGGCTCTTTGGGGAGGCCGGGCCAGCGTCGGGAGTCGGCAGCAGCGGCGGCGGCGGCAGCGGCAG AGGCTCTTTGGGGAGGCCGGGCCAGCGTCGGGCGTCGGCAGCAGCGGCGGCGGCGGCAGCGGCAG A C ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140401826..140436200 26863196 MeRIP-seq:(Medium) rs953900550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250076,Human_RBP_ID_840138,Human_RBP_ID_3967447,Human_RBP_ID_5326886,Human_RBP_ID_5397493,Human_RBP_ID_5532043,Human_RBP_ID_8894155,Human_RBP_ID_9306671,Human_RBP_ID_9354599,Human_RBP_ID_22099714,Human_RBP_ID_26771543 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 109805 RMVar_ID_109805 Human_SNP_ID_253683169 m1A Human chr5 + 140402142 140402136 140402142 GGGAGGCCGGGCCAGCGTCGGGAGTCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC GGGAGGCCGGGCCAGCGTCGGGAGTCG______GCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC GGCAGCA G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:140401826..140402275;chr5:140402104..140402275 26863196 MeRIP-seq:(Medium) rs754392143 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_250076,Human_RBP_ID_3968219,Human_RBP_ID_5326886,Human_RBP_ID_5397493,Human_RBP_ID_5532043,Human_RBP_ID_8894155,Human_RBP_ID_9306671,Human_RBP_ID_9354599,Human_RBP_ID_22099714,Human_RBP_ID_26771543 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 109806 RMVar_ID_109806 Human_SNP_ID_253683170 m1A Human chr5 + 140402142 140402136 140402142 GGGAGGCCGGGCCAGCGTCGGGAGTCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC GGGAGGCCGGGCCAGCGTCGGGAGTCGGCA___GCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC GGCAGCA GGCA ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:140401826..140402275;chr5:140402104..140402275 26863196 MeRIP-seq:(Medium) rs754392143 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_250076,Human_RBP_ID_3968219,Human_RBP_ID_5326886,Human_RBP_ID_5397493,Human_RBP_ID_5532043,Human_RBP_ID_8894155,Human_RBP_ID_9306671,Human_RBP_ID_9354599,Human_RBP_ID_22099714,Human_RBP_ID_26771543 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 109807 RMVar_ID_109807 Human_SNP_ID_253683173 m1A Human chr5 + 140402142 140402142 140402142 GGGAGGCCGGGCCAGCGTCGGGAGTCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC GGGAGGCCGGGCCAGCGTCGGGAGTCGGCAGCGGCGGCGGCGGCGGCAGCGGCAGCGGTACGGGC A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr5:140401826..140402275;chr5:140402104..140402275 26863196 MeRIP-seq:(Medium) rs1561664355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250076,Human_RBP_ID_3968219,Human_RBP_ID_5326886,Human_RBP_ID_5397493,Human_RBP_ID_5532043,Human_RBP_ID_8894155,Human_RBP_ID_9306671,Human_RBP_ID_9354599,Human_RBP_ID_22099714,Human_RBP_ID_26771543 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 109808 RMVar_ID_109808 Human_SNP_ID_253713103 m1A Human chr5 + 140524178 140524178 140524178 ACAGAAAAGGAAACAGGAAGAAGATGAAGAAAACAAACCTAAGGAGAATTCGGAACTACCAGAGG ACAGAAAAGGAAACAGGAAGAAGATGAAGAAAGCAAACCTAAGGAGAATTCGGAACTACCAGAGG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:140524080..140525997 26863196 MeRIP-seq:(Medium) rs369260709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75125,Human_RBP_ID_944602,Human_RBP_ID_2956907,Human_RBP_ID_5610392,Human_RBP_ID_7394667,Human_RBP_ID_8236862,Human_RBP_ID_8885303,Human_RBP_ID_17707153,Human_RBP_ID_18471946,Human_RBP_ID_18537780,Human_RBP_ID_22100707,Human_RBP_ID_24548025,Human_RBP_ID_24554398,Human_RBP_ID_26351425 Human_Splice_Rec_699367,Human_Splice_Rec_699431,Human_Splice_Rec_699499,Human_Splice_Rec_699633,Human_Splice_Rec_699651,Human_Splice_Rec_699751 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972,RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_123847,RMVar_hsa_circ_234985,RMVar_hsa_circ_234993,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_235002,RMVar_hsa_circ_356212,RMVar_hsa_circ_124986,RMVar_hsa_circ_235008,RMVar_hsa_circ_26198,RMVar_hsa_circ_7098,RMVar_hsa_circ_30477,RMVar_hsa_circ_320290,RMVar_hsa_circ_235010,RMVar_hsa_circ_331453,RMVar_hsa_circ_235015,RMVar_hsa_circ_367468,RMVar_hsa_circ_26682,RMVar_hsa_circ_58182,RMVar_hsa_circ_69463,RMVar_hsa_circ_64639,RMVar_hsa_circ_235019,RMVar_hsa_circ_373450,RMVar_hsa_circ_105948,RMVar_hsa_circ_57890,RMVar_hsa_circ_235020 109809 RMVar_ID_109809 Human_SNP_ID_253713954 m1A Human chr5 + 140527882 140527882 140527882 CATGTGTATTCTTCATTTTATAGGTCAAAGAAATTGTCTGTTCCAGCCTCAGTGGTGTCGAGGAT CATGTGTATTCTTCATTTTATAGGTCAAAGAAGTTGTCTGTTCCAGCCTCAGTGGTGTCGAGGAT A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140527877..140527977 26863196 MeRIP-seq:(Medium) rs750061065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2901045,Human_RBP_ID_5532061,Human_RBP_ID_9398359,Human_RBP_ID_24087006,Human_RBP_ID_26351431,Human_RBP_ID_27825911 Human_Splice_Rec_699372,Human_Splice_Rec_699436,Human_Splice_Rec_699638,Human_Splice_Rec_699656,Human_Splice_Rec_699670,Human_Splice_Rec_699684,Human_Splice_Rec_699756 Human_miRNA_ID_2713291,Human_miRNA_ID_2713292,Human_miRNA_ID_3049271,Human_miRNA_ID_3049272 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972,RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_123847,RMVar_hsa_circ_234985,RMVar_hsa_circ_234993,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_356212,RMVar_hsa_circ_124986,RMVar_hsa_circ_235008,RMVar_hsa_circ_26198,RMVar_hsa_circ_7098,RMVar_hsa_circ_30477,RMVar_hsa_circ_320290,RMVar_hsa_circ_235010,RMVar_hsa_circ_331453,RMVar_hsa_circ_235015,RMVar_hsa_circ_367468,RMVar_hsa_circ_26682,RMVar_hsa_circ_69463,RMVar_hsa_circ_64639,RMVar_hsa_circ_57890,RMVar_hsa_circ_72161,RMVar_hsa_circ_96474,RMVar_hsa_circ_235021 109810 RMVar_ID_109810 Human_SNP_ID_253719429 m1A Human chr5 - 140550445 140550445 140550445 CGGTGCCAAGCTAGTCCCCTCTGGTGTCCTCGACTGCCCTGCTCCCTGTGTATCTGCAAACCTCT CGGTGCCAAGCTAGTCCCCTCTGGTGTCCTCGGCTGCCCTGCTCCCTGTGTATCTGCAAACCTCT T C SRA1 Ensembl:ENSG00000213523 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140550344..140550445 32194978 MeRIP-seq:(Medium) rs960959956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2901097,Human_RBP_ID_3760080 109811 RMVar_ID_109811 Human_SNP_ID_253719523 m1A Human chr5 + 140550742 140550742 140550742 TGCTGGAAGCCTGGTATGGTATGGTTCTTCTCAGCTGTGGCTGCAGATTTCTCTTCATTGGCTGC TGCTGGAAGCCTGGTATGGTATGGTTCTTCTCGGCTGTGGCTGCAGATTTCTCTTCATTGGCTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140550691..140550859 26863196 MeRIP-seq:(Medium) rs1179907198 Functional Loss SNV dbSNP153 33..33 33 - - - 109812 RMVar_ID_109812 Human_SNP_ID_253720021 m1A Human chr5 + 140552184 140552184 140552184 GGGGAGGCCCAGGAGAAGTCTCTGATGCGGGGACTGAAAAGGTACAGCAGGATCAAGCAACATGG GGGGAGGCCCAGGAGAAGTCTCTGATGCGGGGGCTGAAAAGGTACAGCAGGATCAAGCAACATGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140552151..140552200 26863196 MeRIP-seq:(Medium) rs773781902 Functional Loss SNV dbSNP153 33..33 33 - - - 109813 RMVar_ID_109813 Human_SNP_ID_253721247 m1A Human chr5 - 140557113 140557113 140557113 TGCGTGGGGCCCCTGTGCTCGGAGACAGACGGAGAATGGGGGGGGGGGGGTGTAAGGCATAAGCC TGCGTGGGGCCCCTGTGCTCGGAGACAGACGGGGAATGGGGGGGGGGGGGTGTAAGGCATAAGCC T C SRA1 Ensembl:ENSG00000213523 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:140557111..140557266 26863196 MeRIP-seq:(Medium) rs1323915815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126400 109814 RMVar_ID_109814 Human_SNP_ID_253721311 m1A Human chr5 + 140557224 140557224 140557224 GCGAGCGCCTGGGTCCGCCGGCCTGGGTCTGCAGCCCGTATGAGAACTGCGGCGGGTCGTTCCAG GCGAGCGCCTGGGTCCGCCGGCCTGGGTCTGCGGCCCGTATGAGAACTGCGGCGGGTCGTTCCAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr5:140557126..140557414;chr5:140557176..140557225 26863410,32194978 MeRIP-seq:(Medium) rs11543165 Functional Loss SNV dbSNP153 33..33 33 - - - 109815 RMVar_ID_109815 Human_SNP_ID_253721396 m1A Human chr5 - 140557381 140557381 140557381 CGGGCTAGGGCACTAGGTTGTCGCCCCGGCCTAGGCTGGGGGCGGTTGCGGCGCTTAGTATGGAC CGGGCTAGGGCACTAGGTTGTCGCCCCGGCCTGGGCTGGGGGCGGTTGCGGCGCTTAGTATGGAC T C SRA1 Ensembl:ENSG00000213523 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:140557319..140557432 26863196 MeRIP-seq:(Medium) rs1014368083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633423,Human_RBP_ID_943819,Human_RBP_ID_27512115 109816 RMVar_ID_109816 Human_SNP_ID_253721480 m1A Human chr5 + 140557442 140557442 140557442 CCCGCCGGCTGCGCTCACCCGGCTTCACGTACAGCTCCGCCATCTCCACTTCCGCTTGGCCAGCG CCCGCCGGCTGCGCTCACCCGGCTTCACGTACGGCTCCGCCATCTCCACTTCCGCTTGGCCAGCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:140557426..140557450 26863410 MeRIP-seq:(Medium) rs1418981103 Functional Loss SNV dbSNP153 33..33 33 - - - 109817 RMVar_ID_109817 Human_SNP_ID_253722108 m1A Human chr5 - 140559529 140559529 140559529 ACGTAGTGAGAGGTGAGATCAGAGAGAATGACAGAAGCCAGGTTTGGGGGACCTCATAGGTCAGG ACGTAGTGAGAGGTGAGATCAGAGAGAATGACTGAAGCCAGGTTTGGGGGACCTCATAGGTCAGG T A APBB3 Ensembl:ENSG00000113108 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140559406..140559591 26863196 MeRIP-seq:(Medium) rs1382277556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24087058 109818 RMVar_ID_109818 Human_SNP_ID_253723466 m1A Human chr5 + 140563799 140563787 140563800 TGCATCTCCTAGTTCCCAGGTTGGGCGCTGCCACTGGGTGCTACCGCTGGGTACATGCCAGTAGT TGCATCTCCTAGTTCCCAGGT_____________TGGGTGCTACCGCTGGGTACATGCCAGTAGT TTGGGCGCTGCCAC T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140563668..140563894 32194978 MeRIP-seq:(Medium) rs1225508693 Functional Loss DEL dbSNP153 22..34 33 - - - 109819 RMVar_ID_109819 Human_SNP_ID_253723471 m1A Human chr5 + 140563799 140563799 140563799 TGCATCTCCTAGTTCCCAGGTTGGGCGCTGCCACTGGGTGCTACCGCTGGGTACATGCCAGTAGT TGCATCTCCTAGTTCCCAGGTTGGGCGCTGCCGCTGGGTGCTACCGCTGGGTACATGCCAGTAGT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140563668..140563894 32194978 MeRIP-seq:(Medium) rs751131035 Functional Loss SNV dbSNP153 33..33 33 - - - 109820 RMVar_ID_109820 Human_SNP_ID_253723597 m1A Human chr5 + 140564247 140564247 140564247 TGATGGCCAGCATGTAATCCTTGCCCAGCATAACCCCGGCTGCTCCCCGCCAGCCTCTGCCGGCC TGATGGCCAGCATGTAATCCTTGCCCAGCATACCCCCGGCTGCTCCCCGCCAGCCTCTGCCGGCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140564155..140564327 26863196 MeRIP-seq:(Medium) rs1020483721 Functional Loss SNV dbSNP153 33..33 33 - - - 109821 RMVar_ID_109821 Human_SNP_ID_253723607 m1A Human chr5 + 140564266 140564266 140564266 CTTGCCCAGCATAACCCCGGCTGCTCCCCGCCAGCCTCTGCCGGCCCGCACTCTCAGCCCAGCGC CTTGCCCAGCATAACCCCGGCTGCTCCCCGCCCGCCTCTGCCGGCCCGCACTCTCAGCCCAGCGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140564163..140564325 26863196 MeRIP-seq:(Medium) rs1441575178 Functional Loss SNV dbSNP153 33..33 33 - - - 109822 RMVar_ID_109822 Human_SNP_ID_253723608 m1A Human chr5 + 140564266 140564266 140564266 CTTGCCCAGCATAACCCCGGCTGCTCCCCGCCAGCCTCTGCCGGCCCGCACTCTCAGCCCAGCGC CTTGCCCAGCATAACCCCGGCTGCTCCCCGCCGGCCTCTGCCGGCCCGCACTCTCAGCCCAGCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140564163..140564325 26863196 MeRIP-seq:(Medium) rs1441575178 Functional Loss SNV dbSNP153 33..33 33 - - - 109823 RMVar_ID_109823 Human_SNP_ID_253723812 m1A Human chr5 + 140564856 140564856 140564856 CAACAAGTTCGGCGGGGAAGATGGCGGATGACAAGGTGAGTGGCCGTGGGGGTGATCTGCAGCCG CAACAAGTTCGGCGGGGAAGATGGCGGATGACGAGGTGAGTGGCCGTGGGGGTGATCTGCAGCCG A G SLC35A4 Ensembl:ENSG00000176087 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr5:140564826..140564875 26863410,26863196 MeRIP-seq:(Medium) rs917918793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846036 Human_Splice_Rec_700149,Human_Splice_Rec_700153,Human_Splice_Rec_700157 RMVar_hsa_circ_79775,RMVar_hsa_circ_235026 109824 RMVar_ID_109824 Human_SNP_ID_253724208 m1A Human chr5 - 140566545 140566545 140566545 ACAGCGAGCCATCCTGCAGAGAAAAATGCAGAAGGAAACTTAGCTAGGCTCCTTCCTGACTGTCC ACAGCGAGCCATCCTGCAGAGAAAAATGCAGAGGGAAACTTAGCTAGGCTCCTTCCTGACTGTCC T C AC116353.5 Ensembl:ENSG00000283155 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140566544..140566727 26863196 MeRIP-seq:(Medium) rs915797632 Functional Loss SNV dbSNP153 33..33 33 - - - 109825 RMVar_ID_109825 Human_SNP_ID_253724209 m1A Human chr5 - 140566545 140566545 140566545 ACAGCGAGCCATCCTGCAGAGAAAAATGCAGAAGGAAACTTAGCTAGGCTCCTTCCTGACTGTCC ACAGCGAGCCATCCTGCAGAGAAAAATGCAGACGGAAACTTAGCTAGGCTCCTTCCTGACTGTCC T G AC116353.5 Ensembl:ENSG00000283155 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140566544..140566727 26863196 MeRIP-seq:(Medium) rs915797632 Functional Loss SNV dbSNP153 33..33 33 - - - 109826 RMVar_ID_109826 Human_SNP_ID_253724210 m1A Human chr5 - 140566553 140566553 140566553 GGAGGACAACAGCGAGCCATCCTGCAGAGAAAAATGCAGAAGGAAACTTAGCTAGGCTCCTTCCT GGAGGACAACAGCGAGCCATCCTGCAGAGAAAGATGCAGAAGGAAACTTAGCTAGGCTCCTTCCT T C AC116353.5 Ensembl:ENSG00000283155 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140566551..140566633 26863196 MeRIP-seq:(Medium) rs1310248676 Functional Loss SNV dbSNP153 33..33 33 - - - 109827 RMVar_ID_109827 Human_SNP_ID_253724235 m1A Human chr5 - 140566672 140566672 140566672 GGCACAGCATATGCCTGAGCCGCATAGATGCCAGTGCAGGTGCCCACAGCAAAGCCCAATACTGC GGCACAGCATATGCCTGAGCCGCATAGATGCCCGTGCAGGTGCCCACAGCAAAGCCCAATACTGC T G AC116353.5 Ensembl:ENSG00000283155 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140565927..140566720 32194978 MeRIP-seq:(Medium) rs1039932554 Functional Loss SNV dbSNP153 33..33 33 - - - 109828 RMVar_ID_109828 Human_SNP_ID_253724497 m1A Human chr5 + 140567402 140567402 140567402 CTCCCTTCTGGTAGGCTGGCAAGCATGGCCCCAGGGGCCCCCACCCTGGCGCCAGGCTGCTCCCT CTCCCTTCTGGTAGGCTGGCAAGCATGGCCCCGGGGGCCCCCACCCTGGCGCCAGGCTGCTCCCT A G SLC35A4 Ensembl:ENSG00000176087 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140567165..140567415 32194978 MeRIP-seq:(Medium) rs1561880220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4813305 Human_miRNA_ID_2295091,Human_miRNA_ID_2436229 RMVar_hsa_circ_79775,RMVar_hsa_circ_84586,RMVar_hsa_circ_235026,RMVar_hsa_circ_235027 109829 RMVar_ID_109829 Human_SNP_ID_253741509 m1A Human chr5 + 140639796 140639796 140639796 GCAGCTGGTCAGCAAGAGGCTGCTGAGAAACGACGCCCCAGAGGAAGCTGGAGAGGGATGTGTGG GCAGCTGGTCAGCAAGAGGCTGCTGAGAAACGGCGCCCCAGAGGAAGCTGGAGAGGGATGTGTGG A G TMCO6 Ensembl:ENSG00000113119 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:140639726..140639875;chr5:140639479..140641024 26863196 MeRIP-seq:(Medium) rs1244079769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_840122,Human_RBP_ID_4813395,Human_RBP_ID_19015937 Human_Splice_Rec_700246,Human_Splice_Rec_700247,Human_Splice_Rec_700268,Human_Splice_Rec_700269,Human_Splice_Rec_700273,Human_Splice_Rec_700278,Human_Splice_Rec_700279,Human_Splice_Rec_700281,Human_Splice_Rec_700283,Human_Splice_Rec_700290,Human_Splice_Rec_700291,Human_Splice_Rec_700297,Human_Splice_Rec_700303,Human_Splice_Rec_700308,Human_Splice_Rec_700309 RMVar_hsa_circ_100736,RMVar_hsa_circ_101112,RMVar_hsa_circ_235028,RMVar_hsa_circ_291414,RMVar_hsa_circ_235029 109830 RMVar_ID_109830 Human_SNP_ID_253743246 m1A Human chr5 - 140645680 140645680 140645680 GAATAGTTAAAGACACCTCCCTCTCTCTCTTCAGCATTTGGCCAAGAGACGAATGTCCCTTTGAA GAATAGTTAAAGACACCTCCCTCTCTCTCTTCCGCATTTGGCCAAGAGACGAATGTCCCTTTGAA T G NDUFA2 Ensembl:ENSG00000131495 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140645668..140645739 26863196 MeRIP-seq:(Medium) rs111312047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633500,Human_RBP_ID_5121415,Human_RBP_ID_9335756 Human_Splice_Rec_700242 Human_miRNA_ID_51146,Human_miRNA_ID_879118,Human_miRNA_ID_1348580,Human_miRNA_ID_1812113 109831 RMVar_ID_109831 Human_SNP_ID_253743817 m1A Human chr5 - 140647492 140647492 140647492 CATCCACTTATGTCAGCGCTCGCCCGGCAGCCAGGGCGTCAGGTGAGGCGCGGCGTGGTGAGGCG CATCCACTTATGTCAGCGCTCGCCCGGCAGCCGGGGCGTCAGGTGAGGCGCGGCGTGGTGAGGCG T C NDUFA2 Ensembl:ENSG00000131495 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140645501..140648106 32194978 MeRIP-seq:(Medium) rs963295784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633504,Human_RBP_ID_4846038,Human_RBP_ID_9335758,Human_RBP_ID_17662724,Human_RBP_ID_18195125,Human_RBP_ID_22458975,Human_RBP_ID_22613468,Human_RBP_ID_27075281 Human_Splice_Rec_700235,Human_Splice_Rec_700239 109832 RMVar_ID_109832 Human_SNP_ID_253743874 m1A Human chr5 - 140647583 140647583 140647583 ACCTGGAATTGGCGACTTCGATATTAACAAGGATGGCGGCGGCCGCAGCAAGTCGAGGAGTCGGG ACCTGGAATTGGCGACTTCGATATTAACAAGGTTGGCGGCGGCCGCAGCAAGTCGAGGAGTCGGG T A NDUFA2 Ensembl:ENSG00000131495 Protein coding start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr5:140647387..140647587 26863410 MeRIP-seq:(Medium) rs1191845349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633507,Human_RBP_ID_1039461,Human_RBP_ID_1646427,Human_RBP_ID_4846039,Human_RBP_ID_5121417,Human_RBP_ID_5449382,Human_RBP_ID_9335758,Human_RBP_ID_17662725,Human_RBP_ID_22458976,Human_RBP_ID_27075284 109833 RMVar_ID_109833 Human_SNP_ID_253744063 m1A Human chr5 - 140647910 140647910 140647910 GGATGGCCTGAGCCTTACTATCTCGCTCCGGCATTTTGTTATCGTTCTTTCGCTGTCACCAACAA GGATGGCCTGAGCCTTACTATCTCGCTCCGGCGTTTTGTTATCGTTCTTTCGCTGTCACCAACAA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:140647826..140647950 26863410 MeRIP-seq:(Medium) rs747563860 Functional Loss SNV dbSNP153 33..33 33 - - - 109834 RMVar_ID_109834 Human_SNP_ID_253744074 m1A Human chr5 - 140647926 140647926 140647926 ATGGGGAAGAAATAACGGATGGCCTGAGCCTTACTATCTCGCTCCGGCATTTTGTTATCGTTCTT ATGGGGAAGAAATAACGGATGGCCTGAGCCTTGCTATCTCGCTCCGGCATTTTGTTATCGTTCTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140647916..140648106 32194978 MeRIP-seq:(Medium) rs749036471 Functional Loss SNV dbSNP153 33..33 33 - - - 109835 RMVar_ID_109835 Human_SNP_ID_253744375 m1A Human chr5 + 140648516 140648516 140648516 CAACCCTTTGGCCCCCGATGGCCACGATGTGGATGATCCTCACTCCTTCCACCAGTGAGTATTTT CAACCCTTTGGCCCCCGATGGCCACGATGTGGTTGATCCTCACTCCTTCCACCAGTGAGTATTTT A T IK Ensembl:ENSG00000113141 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:140648451..140648550 26863196 MeRIP-seq:(Medium) rs1194357416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8894171,Human_RBP_ID_9398367,Human_RBP_ID_26351438 Human_Splice_Rec_700372,Human_Splice_Rec_700373,Human_Splice_Rec_700380,Human_Splice_Rec_700381,Human_Splice_Rec_700388,Human_Splice_Rec_700389,Human_Splice_Rec_700424,Human_Splice_Rec_700425,Human_Splice_Rec_700432,Human_Splice_Rec_700433,Human_Splice_Rec_700448,Human_Splice_Rec_700449,Human_Splice_Rec_700456,Human_Splice_Rec_700457,Human_Splice_Rec_700469 109836 RMVar_ID_109836 Human_SNP_ID_253745548 m1A Human chr5 - 140653124 140653124 140653124 CTCAGTACTCACGCCTCAGCAGTGGGGCCAACAGCCCTATAGTTAGCTGTGGTGCTGATAAGCTC CTCAGTACTCACGCCTCAGCAGTGGGGCCAACCGCCCTATAGTTAGCTGTGGTGCTGATAAGCTC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140652094..140653966 32194978 MeRIP-seq:(Medium) rs943751410 Functional Loss SNV dbSNP153 33..33 33 - - - 109837 RMVar_ID_109837 Human_SNP_ID_253745833 m1A Human chr5 + 140653929 140653929 140653929 CTGGACAGTACTGTTCTTATGTGGCCTCTTTCATTATACAGGGACAAATCAGCTGCAGAGAAGAG CTGGACAGTACTGTTCTTATGTGGCCTCTTTCGTTATACAGGGACAAATCAGCTGCAGAGAAGAG A G IK Ensembl:ENSG00000113141 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140653926..140654000 26863196 MeRIP-seq:(Medium) rs201879338 Functional Loss SNV dbSNP153 33..33 33 - - - 109838 RMVar_ID_109838 Human_SNP_ID_253747057 m1A Human chr5 + 140659036 140659036 140659036 AGAGATATCGGGAACGGGAGCGTGATCGGGAAAGAGACAGAGACCGTGACCGAGAGCGAGAGCGA AGAGATATCGGGAACGGGAGCGTGATCGGGAAGGAGACAGAGACCGTGACCGAGAGCGAGAGCGA A G IK Ensembl:ENSG00000113141 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:140658926..140659319;chr5:140658726..140659319 26863196 MeRIP-seq:(Medium) rs955531238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839786,Human_RBP_ID_9306697,Human_RBP_ID_9398381,Human_RBP_ID_22100258,Human_RBP_ID_24087129,Human_RBP_ID_24548268,Human_RBP_ID_26351454,Human_RBP_ID_27826884 Human_Splice_Rec_700408,Human_Splice_Rec_700472 RMVar_hsa_circ_14075,RMVar_hsa_circ_76569,RMVar_hsa_circ_108069,RMVar_hsa_circ_235035,RMVar_hsa_circ_119812,RMVar_hsa_circ_235036,RMVar_hsa_circ_110805,RMVar_hsa_circ_235037,RMVar_hsa_circ_235038 109839 RMVar_ID_109839 Human_SNP_ID_253747286 m1A Human chr5 + 140659823 140659823 140659823 AATGAAAAGTTTGCTGGGTCTGCTGGCTGGGAAGGCACAGAATCATATCCTTTATTTTAATACGT AATGAAAAGTTTGCTGGGTCTGCTGGCTGGGAGGGCACAGAATCATATCCTTTATTTTAATACGT A G IK Ensembl:ENSG00000113141 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:140659801..140659825 26863196 MeRIP-seq:(Medium) rs1253186086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943822,Human_RBP_ID_9399498,Human_RBP_ID_22100259,Human_RBP_ID_26352658,Human_RBP_ID_27825930 Human_Splice_Rec_700412,Human_Splice_Rec_700476,Human_Splice_Rec_700488 RMVar_hsa_circ_76569,RMVar_hsa_circ_119812,RMVar_hsa_circ_235036,RMVar_hsa_circ_235037,RMVar_hsa_circ_336176 109840 RMVar_ID_109840 Human_SNP_ID_253747758 m1A Human chr5 + 140661640 140661640 140661640 GTCCTGCAACAGGGTAACAAGAAGGGGCCCTTAGGCCGTTGGGACTTTGATACCCAGGAAGAATA GTCCTGCAACAGGGTAACAAGAAGGGGCCCTTGGGCCGTTGGGACTTTGATACCCAGGAAGAATA A G IK Ensembl:ENSG00000113141 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:140661626..140661650 26863196 MeRIP-seq:(Medium) rs953312692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74211,Human_RBP_ID_943825,Human_RBP_ID_1988781,Human_RBP_ID_3760122,Human_RBP_ID_3967469,Human_RBP_ID_4813467,Human_RBP_ID_5151335,Human_RBP_ID_7394913,Human_RBP_ID_18834298,Human_RBP_ID_19015159,Human_RBP_ID_26351468,Human_RBP_ID_27075297,Human_RBP_ID_27825934 Human_Splice_Rec_700416,Human_Splice_Rec_700417,Human_Splice_Rec_700480,Human_Splice_Rec_700481,Human_Splice_Rec_700491 RMVar_hsa_circ_76569,RMVar_hsa_circ_119812,RMVar_hsa_circ_235036,RMVar_hsa_circ_235037 109841 RMVar_ID_109841 Human_SNP_ID_253748539 m1A Human chr5 + 140664952 140664952 140664952 GCACTTGTGAGGAGAGGCCCGCTGAGGATGGGAGCGACGAGGAGGACCCAGACTCCATGGAAGCC GCACTTGTGAGGAGAGGCCCGCTGAGGATGGGTGCGACGAGGAGGACCCAGACTCCATGGAAGCC A T WDR55 Ensembl:ENSG00000120314 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140664903..140665034 26863196 MeRIP-seq:(Medium) rs1461197380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4813486,Human_RBP_ID_23050287 109842 RMVar_ID_109842 Human_SNP_ID_253748610 m1A Human chr5 + 140665117 140665117 140665117 TGGACGGGGACGTGTTCGTGTGAGAGCGGGGCAGGGCCGGGGCGCCGGGTCTGGAAGCTTCCCGG TGGACGGGGACGTGTTCGTGTGAGAGCGGGGCCGGGCCGGGGCGCCGGGTCTGGAAGCTTCCCGG A C WDR55 Ensembl:ENSG00000120314 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140665109..140665188 26863196 MeRIP-seq:(Medium) rs973045601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124768,Human_RBP_ID_26352666 109843 RMVar_ID_109843 Human_SNP_ID_253749827 m1A Human chr5 - 140669558 140669558 140669558 CTCAGTCCTGCGAAGAAGTCATCGGTGCTCCAAGTCTTGCTGCTCAGAGCCCGCAGTGGTCCTCC CTCAGTCCTGCGAAGAAGTCATCGGTGCTCCACGTCTTGCTGCTCAGAGCCCGCAGTGGTCCTCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140669507..140669703 26863196 MeRIP-seq:(Medium) rs1279431763 Functional Loss SNV dbSNP153 33..33 33 - - - 109844 RMVar_ID_109844 Human_SNP_ID_253750308 m1A Human chr5 - 140671310 140671310 140671310 ACCTCCTGTGGTCTGCTGGGGCTGAGGCAGGTACCATGGTTAAACAGTGACTCCATTCTTTCTCC ACCTCCTGTGGTCTGCTGGGGCTGAGGCAGGTCCCATGGTTAAACAGTGACTCCATTCTTTCTCC T G DND1 Ensembl:ENSG00000256453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140671222..140671322 32194978 MeRIP-seq:(Medium) rs767711054 Functional Loss SNV dbSNP153 33..33 33 - - - 109845 RMVar_ID_109845 Human_SNP_ID_253750486 m1A Human chr5 + 140671719 140671719 140671719 CGCTGCTTCAGGTCTGGCTTGAGCCACTCCACAGCCACCTGCTCTCCACAGAGGTGTGACTGCCC CGCTGCTTCAGGTCTGGCTTGAGCCACTCCACGGCCACCTGCTCTCCACAGAGGTGTGACTGCCC A G WDR55 Ensembl:ENSG00000120314 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140671670..140671771 32194978 MeRIP-seq:(Medium) rs141336765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24386609 109846 RMVar_ID_109846 Human_SNP_ID_253751071 m1A Human chr5 + 140673380 140673380 140673380 AGCGCCGCCTTGTTCTCTGGATTCACCCTCTCACACCACAGCTGAGAGGGAAAGGAAGGTTGGAA AGCGCCGCCTTGTTCTCTGGATTCACCCTCTCCCACCACAGCTGAGAGGGAAAGGAAGGTTGGAA A C WDR55 Ensembl:ENSG00000120314 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140673027..140673476 32194978 MeRIP-seq:(Medium) rs1346716259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18040625 109847 RMVar_ID_109847 Human_SNP_ID_253751533 m1A Human chr5 - 140674776 140674776 140674776 GAAGAACCCAAAGCTACTGAACCAGTTACAGTACTGTGAGGAGGCAGGCATCCCACTGGTGGCTA GAAGAACCCAAAGCTACTGAACCAGTTACAGTCCTGTGAGGAGGCAGGCATCCCACTGGTGGCTA T G HARS1 Ensembl:ENSG00000170445 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140674726..140674775 32194978 MeRIP-seq:(Medium) rs387906639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1646463,Human_RBP_ID_1988802,Human_RBP_ID_2901199,Human_RBP_ID_3760144,Human_RBP_ID_7394958,Human_RBP_ID_8605064,Human_RBP_ID_9398397,Human_RBP_ID_15328068,Human_RBP_ID_18448209,Human_RBP_ID_26352668 Human_Splice_Rec_700566,Human_Splice_Rec_700567,Human_Splice_Rec_700584,Human_Splice_Rec_700585,Human_Splice_Rec_700608,Human_Splice_Rec_700609,Human_Splice_Rec_700630,Human_Splice_Rec_700631,Human_Splice_Rec_700652,Human_Splice_Rec_700653,Human_Splice_Rec_700674,Human_Splice_Rec_700675,Human_Splice_Rec_700700,Human_Splice_Rec_700701,Human_Splice_Rec_700726,Human_Splice_Rec_700727,Human_Splice_Rec_700752,Human_Splice_Rec_700753,Human_Splice_Rec_700778,Human_Splice_Rec_700779,Human_Splice_Rec_700782,Human_Splice_Rec_700783,Human_Splice_Rec_700802,Human_Splice_Rec_700803 Human_miRNA_ID_1934894,Human_miRNA_ID_1993163,Human_miRNA_ID_2285021,Human_miRNA_ID_2288021 Clinvar_Rec_736 GWAS_ID_15316,GWAS_ID_15317 RMVar_hsa_circ_107708,RMVar_hsa_circ_124816,RMVar_hsa_circ_118846,RMVar_hsa_circ_235046,RMVar_hsa_circ_90848,RMVar_hsa_circ_100013,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_235047,RMVar_hsa_circ_235050,RMVar_hsa_circ_235045 109848 RMVar_ID_109848 Human_SNP_ID_253751541 m1A Human chr5 - 140674810 140674810 140674810 GCTCTTGTCCCCTGCAGGCTGAGCTGCTGTACAAGAAGAACCCAAAGCTACTGAACCAGTTACAG GCTCTTGTCCCCTGCAGGCTGAGCTGCTGTACGAGAAGAACCCAAAGCTACTGAACCAGTTACAG T C HARS1 Ensembl:ENSG00000170445 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140674676..140674850 26863196 MeRIP-seq:(Medium) rs1200977462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946170,Human_RBP_ID_3760144,Human_RBP_ID_3967470,Human_RBP_ID_8605065,Human_RBP_ID_9398398,Human_RBP_ID_18834316,Human_RBP_ID_26352669 Human_Splice_Rec_700566,Human_Splice_Rec_700584,Human_Splice_Rec_700608,Human_Splice_Rec_700630,Human_Splice_Rec_700652,Human_Splice_Rec_700674,Human_Splice_Rec_700700,Human_Splice_Rec_700726,Human_Splice_Rec_700752,Human_Splice_Rec_700778,Human_Splice_Rec_700782,Human_Splice_Rec_700802 RMVar_hsa_circ_107708,RMVar_hsa_circ_124816,RMVar_hsa_circ_118846,RMVar_hsa_circ_235046,RMVar_hsa_circ_90848,RMVar_hsa_circ_100013,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_235047,RMVar_hsa_circ_235050,RMVar_hsa_circ_235045 109849 RMVar_ID_109849 Human_SNP_ID_253751542 m1A Human chr5 - 140674810 140674810 140674810 GCTCTTGTCCCCTGCAGGCTGAGCTGCTGTACAAGAAGAACCCAAAGCTACTGAACCAGTTACAG GCTCTTGTCCCCTGCAGGCTGAGCTGCTGTACCAGAAGAACCCAAAGCTACTGAACCAGTTACAG T G HARS1 Ensembl:ENSG00000170445 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140674676..140674850 26863196 MeRIP-seq:(Medium) rs1200977462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_946170,Human_RBP_ID_3760144,Human_RBP_ID_3967470,Human_RBP_ID_8605065,Human_RBP_ID_9398398,Human_RBP_ID_18834316,Human_RBP_ID_26352669 Human_Splice_Rec_700566,Human_Splice_Rec_700584,Human_Splice_Rec_700608,Human_Splice_Rec_700630,Human_Splice_Rec_700652,Human_Splice_Rec_700674,Human_Splice_Rec_700700,Human_Splice_Rec_700726,Human_Splice_Rec_700752,Human_Splice_Rec_700778,Human_Splice_Rec_700782,Human_Splice_Rec_700802 RMVar_hsa_circ_107708,RMVar_hsa_circ_124816,RMVar_hsa_circ_118846,RMVar_hsa_circ_235046,RMVar_hsa_circ_90848,RMVar_hsa_circ_100013,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_235047,RMVar_hsa_circ_235050,RMVar_hsa_circ_235045 109850 RMVar_ID_109850 Human_SNP_ID_253752362 m1A Human chr5 - 140677886 140677886 140677886 TCCTGGTCAAGGTCAGAGCTGACAAGGCTGGGAGGGCAAAGTTGGGCCTGGCCTCTCACAAGAGA TCCTGGTCAAGGTCAGAGCTGACAAGGCTGGGTGGGCAAAGTTGGGCCTGGCCTCTCACAAGAGA T A HARS1 Ensembl:ENSG00000170445 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140677882..140677983 32194978 MeRIP-seq:(Medium) rs367875444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1646470,Human_RBP_ID_5397512,Human_RBP_ID_18834323,Human_RBP_ID_19124774 RMVar_hsa_circ_107708,RMVar_hsa_circ_90848,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_54543,RMVar_hsa_circ_305418,RMVar_hsa_circ_364806 109851 RMVar_ID_109851 Human_SNP_ID_253752451 m1A Human chr5 - 140678190 140678189 140678191 GAAGGAATAGCCCAGTAGATGGAAAGGAAACCAAAACTGGTGAGAAGCCCAAAGATGCCGGGGTT GAAGGAATAGCCCAGTAGATGGAAAGGAAAC__AAACTGGTGAGAAGCCCAAAGATGCCGGGGTT TTG T HARS1 Ensembl:ENSG00000170445 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140678181..140678282 32194978 MeRIP-seq:(Medium) rs1162201937 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_107708,RMVar_hsa_circ_90848,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_305418,RMVar_hsa_circ_364806,RMVar_hsa_circ_235052,RMVar_hsa_circ_375320 109852 RMVar_ID_109852 Human_SNP_ID_253755400 m1A Human chr5 - 140690906 140690906 140690906 GAGGAGGTGGCGAAACTCCTGAAACTGAAGGCACAGCTGGGTCCTGATGAAAGCAAACAGAAATT GAGGAGGTGGCGAAACTCCTGAAACTGAAGGCCCAGCTGGGTCCTGATGAAAGCAAACAGAAATT T G HARS1 Ensembl:ENSG00000170445 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140690851..140690950 26863196 MeRIP-seq:(Medium) rs778485839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788364,Human_RBP_ID_943832,Human_RBP_ID_1319678,Human_RBP_ID_1988828,Human_RBP_ID_3967473,Human_RBP_ID_5396796,Human_RBP_ID_9170739,Human_RBP_ID_18834345,Human_RBP_ID_19015975,Human_RBP_ID_19124777,Human_RBP_ID_26351477,Human_RBP_ID_27826903 Human_Splice_Rec_700546,Human_Splice_Rec_700547,Human_Splice_Rec_700570,Human_Splice_Rec_700571,Human_Splice_Rec_700588,Human_Splice_Rec_700589,Human_Splice_Rec_700634,Human_Splice_Rec_700635,Human_Splice_Rec_700656,Human_Splice_Rec_700657,Human_Splice_Rec_700678,Human_Splice_Rec_700679,Human_Splice_Rec_700704,Human_Splice_Rec_700705,Human_Splice_Rec_700730,Human_Splice_Rec_700731,Human_Splice_Rec_700756,Human_Splice_Rec_700757,Human_Splice_Rec_700786,Human_Splice_Rec_700787,Human_Splice_Rec_700806,Human_Splice_Rec_700807,Human_Splice_Rec_700818,Human_Splice_Rec_700819,Human_Splice_Rec_700830,Human_Splice_Rec_700831,Human_Splice_Rec_700836,Human_Splice_Rec_700837 RMVar_hsa_circ_90848,RMVar_hsa_circ_235049 109853 RMVar_ID_109853 Human_SNP_ID_253755414 m1A Human chr5 + 140690943 140690943 140690943 TCAGTTTCAGGAGTTTCGCCACCTCCTCCTCGATCTGTGGAGGGAAAGAAGGCGCTGAGCTATCC TCAGTTTCAGGAGTTTCGCCACCTCCTCCTCGGTCTGTGGAGGGAAAGAAGGCGCTGAGCTATCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140690905..140691325 32194978 MeRIP-seq:(Medium) rs1321938423 Functional Loss SNV dbSNP153 33..33 33 - - - 109854 RMVar_ID_109854 Human_SNP_ID_253755709 m1A Human chr5 - 140691650 140691650 140691650 AGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCATCGCGCGGCAGGACGCCGGCTTTCCGGGACAG AGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCTTCGCGCGGCAGGACGCCGGCTTTCCGGGACAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140691518..140691710 26863196 MeRIP-seq:(Medium) rs1320493173 Functional Loss SNV dbSNP153 33..33 33 - - - 109855 RMVar_ID_109855 Human_SNP_ID_253755710 m1A Human chr5 - 140691650 140691650 140691650 AGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCATCGCGCGGCAGGACGCCGGCTTTCCGGGACAG AGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCCTCGCGCGGCAGGACGCCGGCTTTCCGGGACAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140691518..140691710 26863196 MeRIP-seq:(Medium) rs1320493173 Functional Loss SNV dbSNP153 33..33 33 - - - 109856 RMVar_ID_109856 Human_SNP_ID_253755724 m1A Human chr5 + 140691673 140691673 140691673 GCCGCGCGATGCCCCTGCTCGGACTTCTTCCCAGGAGGGCCTGGGCTTCGCTGCTCAGCCAGCTC GCCGCGCGATGCCCCTGCTCGGACTTCTTCCCGGGAGGGCCTGGGCTTCGCTGCTCAGCCAGCTC A G HARS2 Ensembl:ENSG00000112855 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:140691512..140691702;chr5:140691554..140691757 26863196 MeRIP-seq:(Medium) rs1207539784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22100520 Human_Splice_Rec_700840,Human_Splice_Rec_700841,Human_Splice_Rec_700861,Human_Splice_Rec_700918,Human_Splice_Rec_700919,Human_Splice_Rec_700945,Human_Splice_Rec_700967,Human_Splice_Rec_701011,Human_Splice_Rec_701035,Human_Splice_Rec_701098,Human_Splice_Rec_701099,Human_Splice_Rec_701127,Human_Splice_Rec_701133,Human_Splice_Rec_701155,Human_Splice_Rec_701169 RMVar_hsa_circ_570 109857 RMVar_ID_109857 Human_SNP_ID_253755725 m1A Human chr5 + 140691673 140691673 140691673 GCCGCGCGATGCCCCTGCTCGGACTTCTTCCCAGGAGGGCCTGGGCTTCGCTGCTCAGCCAGCTC GCCGCGCGATGCCCCTGCTCGGACTTCTTCCCTGGAGGGCCTGGGCTTCGCTGCTCAGCCAGCTC A T HARS2 Ensembl:ENSG00000112855 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr5:140691512..140691702;chr5:140691554..140691757 26863196 MeRIP-seq:(Medium) rs1207539784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22100520 Human_Splice_Rec_700840,Human_Splice_Rec_700841,Human_Splice_Rec_700861,Human_Splice_Rec_700918,Human_Splice_Rec_700919,Human_Splice_Rec_700945,Human_Splice_Rec_700967,Human_Splice_Rec_701011,Human_Splice_Rec_701035,Human_Splice_Rec_701098,Human_Splice_Rec_701099,Human_Splice_Rec_701127,Human_Splice_Rec_701133,Human_Splice_Rec_701155,Human_Splice_Rec_701169 RMVar_hsa_circ_570 109858 RMVar_ID_109858 Human_SNP_ID_253755730 m1A Human chr5 - 140691682 140691682 140691682 CGGTCGCAGGAGCTGGCTGAGCAGCGAAGCCCAGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCA CGGTCGCAGGAGCTGGCTGAGCAGCGAAGCCCGGGCCCTCCTGGGAAGAAGTCCGAGCAGGGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140691524..140691725 32194978 MeRIP-seq:(Medium) rs575626648 Functional Loss SNV dbSNP153 33..33 33 - - - 109859 RMVar_ID_109859 Human_SNP_ID_253757337 m1A Human chr5 - 140697282 140697282 140697282 CCACCAGCCCATCATAGCGCCCACCAGCAGCCACACTGCCCACATTCAGGGGCTCCTCCCCAGCC CCACCAGCCCATCATAGCGCCCACCAGCAGCCGCACTGCCCACATTCAGGGGCTCCTCCCCAGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140697233..140697425 26863196 MeRIP-seq:(Medium) rs778446302 Functional Loss SNV dbSNP153 33..33 33 - - - 109860 RMVar_ID_109860 Human_SNP_ID_253758168 m1A Human chr5 - 140700480 140700480 140700480 CCCGCAAAACCTCCTCCTCAGACACAACACCTACCCCGCTGCCCGACGCCATCTTCACAGCGAAG CCCGCAAAACCTCCTCCTCAGACACAACACCTGCCCCGCTGCCCGACGCCATCTTCACAGCGAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:140700451..140700500 26863196 MeRIP-seq:(Medium) rs1562069605 Functional Loss SNV dbSNP153 33..33 33 - - - 109861 RMVar_ID_109861 Human_SNP_ID_253758304 m1A Human chr5 - 140700911 140700911 140700911 ACCCTTAGCCCTTGATGTAGTTAGCACCCACCATCTTTCTTTTCTCTCTCTTCCGTGAGCCTCTT ACCCTTAGCCCTTGATGTAGTTAGCACCCACCGTCTTTCTTTTCTCTCTCTTCCGTGAGCCTCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140700801..140700925 26863196 MeRIP-seq:(Medium) rs753285675 Functional Loss SNV dbSNP153 33..33 33 - - - 109862 RMVar_ID_109862 Human_SNP_ID_253759214 m1A Human chr5 + 140704551 140704551 140704551 AGAAGCAGAAGGATTATGATTTTGAGGAAAGGATGAAGGAGCTCAGAGAAGAGGTAAGGGTCTCC AGAAGCAGAAGGATTATGATTTTGAGGAAAGGTTGAAGGAGCTCAGAGAAGAGGTAAGGGTCTCC A T ZMAT2 Ensembl:ENSG00000146007 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140704501..140704575 32194978 MeRIP-seq:(Medium) rs1222587131 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_943046,Human_RBP_ID_3760170,Human_RBP_ID_5656005,Human_RBP_ID_7395107,Human_RBP_ID_9349711,Human_RBP_ID_9398406,Human_RBP_ID_19015174,Human_RBP_ID_21990316,Human_RBP_ID_23050289,Human_RBP_ID_24087218,Human_RBP_ID_24548136,Human_RBP_ID_26351482,Human_RBP_ID_27825946 Human_Splice_Rec_701219,Human_Splice_Rec_701229 109863 RMVar_ID_109863 Human_SNP_ID_253759500 m1A Human chr5 + 140705617 140705617 140705617 ACTGATTCTGAGTGATTTTTCCCTCCAGGAGGAAAAGGCCAAAGCGTACAAGAAAGAGAAACAGA ACTGATTCTGAGTGATTTTTCCCTCCAGGAGGGAAAGGCCAAAGCGTACAAGAAAGAGAAACAGA A G ZMAT2 Ensembl:ENSG00000146007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:140704426..140705850;chr5:140704451..140705850 26863196 MeRIP-seq:(Medium) rs766552234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_943047,Human_RBP_ID_5656006,Human_RBP_ID_9398407,Human_RBP_ID_24548137,Human_RBP_ID_26351483 Human_Splice_Rec_701220,Human_Splice_Rec_701230 109864 RMVar_ID_109864 Human_SNP_ID_253830868 m1A Human chr5 + 140966643 140966642 140966643 CTACGGAGGGAGCGGCCCCAGGCGCTTTCTAGAGCGTGAGCGGTGGGGGAGCAGGCGCAGGGTGG CTACGGAGGGAGCGGCCCCAGGCGCTTTCTAG_GCGTGAGCGGTGGGGGAGCAGGCGCAGGGTGG GA G PCDHA1,PCDHA6,PCDHAC2,PCDHA11,PCDHA5,PCDHA3,PCDHA4,PCDHA12,PCDHA9,PCDHAC1,PCDHA7,PCDHA8,PCDHA2,PCDHA10,PCDHA13 Ensembl:ENSG00000204970,Ensembl:ENSG00000081842,Ensembl:ENSG00000243232,Ensembl:ENSG00000249158,Ensembl:ENSG00000204965,Ensembl:ENSG00000255408,Ensembl:ENSG00000204967,Ensembl:ENSG00000251664,Ensembl:ENSG00000204961,Ensembl:ENSG00000248383,Ensembl:ENSG00000204963,Ensembl:ENSG00000204962,Ensembl:ENSG00000204969,Ensembl:ENSG00000250120,Ensembl:ENSG00000239389 Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,5'UTR,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140966593..140966676 26863196 MeRIP-seq:(Medium) rs1563353190 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_235065 109865 RMVar_ID_109865 Human_SNP_ID_253830871 m1A Human chr5 - 140966654 140966644 140966654 CTCCGCTCGTGCCACCCTGCGCCTGCTCCCCCACCGCTCACGCTCTAGAAAGCGCCTGGGGCCGC CTCCGCTCGTGCCACCCTGCGCCTGCTCCCCC__________CTCTAGAAAGCGCCTGGGGCCGC GCGTGAGCGGT G RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140966557..140966756 26863196 MeRIP-seq:(Medium) rs1554228519 Functional Loss DEL dbSNP153 33..42 33 - - - 109866 RMVar_ID_109866 Human_SNP_ID_253830874 m1A Human chr5 - 140966654 140966654 140966654 CTCCGCTCGTGCCACCCTGCGCCTGCTCCCCCACCGCTCACGCTCTAGAAAGCGCCTGGGGCCGC CTCCGCTCGTGCCACCCTGCGCCTGCTCCCCCCCCGCTCACGCTCTAGAAAGCGCCTGGGGCCGC T G RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140966557..140966756 26863196 MeRIP-seq:(Medium) rs1048894569 Functional Loss SNV dbSNP153 33..33 33 - - - 109867 RMVar_ID_109867 Human_SNP_ID_253887190 m1A Human chr5 + 141187195 141187190 141187195 TGAGACAGATGGGCTGAGAAGAAGAGCTGTCGAGTCCCTGATTGGGAAAGGAAAAATTAAAAACC TGAGACAGATGGGCTGAGAAGAAGAGCT_____GTCCCTGATTGGGAAAGGAAAAATTAAAAACC TGTCGA T PCDHB9,AC244517.6 Ensembl:ENSG00000177839,Ensembl:ENSG00000279068 Protein coding,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141187179..141187299 26863196 MeRIP-seq:(Medium) rs1339206824 Functional Loss DEL dbSNP153 29..33 33 - - - 109868 RMVar_ID_109868 Human_SNP_ID_253925134 m1A Human chr5 + 141319305 141319305 141319305 GTAGCTGTCTCTCCAGATCTTCCTCCGTGTCAATGATGTTTATATCTTCTTCATCTTGATGCTGG GTAGCTGTCTCTCCAGATCTTCCTCCGTGTCAGTGATGTTTATATCTTCTTCATCTTGATGCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141319254..141319329 26863196 MeRIP-seq:(Medium) rs1295617343 Functional Loss SNV dbSNP153 33..33 33 - - - 109869 RMVar_ID_109869 Human_SNP_ID_253925510 m1A Human chr5 - 141320718 141320718 141320718 AGGGCCGGCGAGGTGCGGGGTCTGGTGATGCGAGCTGCGCCTCTCGGCAAGATTTCGCGCTGCCC AGGGCCGGCGAGGTGCGGGGTCTGGTGATGCGGGCTGCGCCTCTCGGCAAGATTTCGCGCTGCCC T C TAF7 Ensembl:ENSG00000178913 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:141320631..141320731 26863410 MeRIP-seq:(Medium) rs907038232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1646613,Human_RBP_ID_4845398,Human_RBP_ID_5103433,Human_RBP_ID_5326887,Human_RBP_ID_5532075,Human_RBP_ID_7492320,Human_RBP_ID_8885451,Human_RBP_ID_9170781,Human_RBP_ID_17209425,Human_RBP_ID_17673937,Human_RBP_ID_17707183,Human_RBP_ID_18040716,Human_RBP_ID_18425317,Human_RBP_ID_18502404,Human_RBP_ID_18834441,Human_RBP_ID_18927250,Human_RBP_ID_21960548,Human_RBP_ID_22365381,Human_RBP_ID_22481935,Human_RBP_ID_22512923,Human_RBP_ID_23050353,Human_RBP_ID_24087393,Human_RBP_ID_26351498,Human_RBP_ID_26771554,Human_RBP_ID_27075420 109870 RMVar_ID_109870 Human_SNP_ID_253925518 m1A Human chr5 - 141320723 141320723 141320723 GACGGAGGGCCGGCGAGGTGCGGGGTCTGGTGATGCGAGCTGCGCCTCTCGGCAAGATTTCGCGC GACGGAGGGCCGGCGAGGTGCGGGGTCTGGTGTTGCGAGCTGCGCCTCTCGGCAAGATTTCGCGC T A TAF7 Ensembl:ENSG00000178913 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141320614..141320775 26863196 MeRIP-seq:(Medium) rs370294489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1646613,Human_RBP_ID_3784753,Human_RBP_ID_4845398,Human_RBP_ID_5090148,Human_RBP_ID_5103433,Human_RBP_ID_5326887,Human_RBP_ID_5532075,Human_RBP_ID_7492320,Human_RBP_ID_8267771,Human_RBP_ID_8885451,Human_RBP_ID_9170781,Human_RBP_ID_9306703,Human_RBP_ID_17303573,Human_RBP_ID_17673937,Human_RBP_ID_17707183,Human_RBP_ID_18040716,Human_RBP_ID_18425317,Human_RBP_ID_18502404,Human_RBP_ID_18927250,Human_RBP_ID_19128524,Human_RBP_ID_21215847,Human_RBP_ID_21960548,Human_RBP_ID_22100262,Human_RBP_ID_22365381,Human_RBP_ID_22481935,Human_RBP_ID_22512923,Human_RBP_ID_23050353,Human_RBP_ID_24087393,Human_RBP_ID_24548212,Human_RBP_ID_26351498,Human_RBP_ID_26771554,Human_RBP_ID_27075420 109871 RMVar_ID_109871 Human_SNP_ID_253973856 m1A Human chr5 - 141478337 141478337 141478337 CAGGCCTCCCCGCACGGCGTCCGCGTGCAAGGAGGGCCCTGGTGTTCGGTACAGTGAGCTCACCG CAGGCCTCCCCGCACGGCGTCCGCGTGCAAGGGGGGCCCTGGTGTTCGGTACAGTGAGCTCACCG T C lnc-DIAPH1-2 RNACentral:URS0000D591C7 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141478288..141478388 32194978 MeRIP-seq:(Medium) rs766980546 Functional Loss SNV dbSNP153 33..33 33 - - - 109872 RMVar_ID_109872 Human_SNP_ID_253982310 m1A Human chr5 - 141511532 141511532 141511532 CGGGAAAGAGGAACTGTTGGAGTGGGGTGGGGAGGAGGGAGGCATGGGATGGATGGGCCTGATTG CGGGAAAGAGGAACTGTTGGAGTGGGGTGGGGCGGAGGGAGGCATGGGATGGATGGGCCTGATTG T G lnc-DIAPH1-2 RNACentral:URS0000D591C7 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:141511481..141511641 32194978 MeRIP-seq:(Medium) rs548369303 Functional Loss SNV dbSNP153 33..33 33 - - - 109873 RMVar_ID_109873 Human_SNP_ID_253982633 m1A Human chr5 - 141512764 141512764 141512764 CAGCACAAAACACAACACGGGCCGCCGCGGGCAGATCAAGGACAGACGGCTGCGCGGAGCCCGCC CAGCACAAAACACAACACGGGCCGCCGCGGGCCGATCAAGGACAGACGGCTGCGCGGAGCCCGCC T G lnc-DIAPH1-2 RNACentral:URS0000D591C7 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:141512529..141512781 32194978 MeRIP-seq:(Medium) rs1006339454 Functional Loss SNV dbSNP153 33..33 33 - - - 109874 RMVar_ID_109874 Human_SNP_ID_253982638 m1A Human chr5 - 141512780 141512780 141512780 CCTTAGCGCGTGGACACAGCACAAAACACAACACGGGCCGCCGCGGGCAGATCAAGGACAGACGG CCTTAGCGCGTGGACACAGCACAAAACACAACGCGGGCCGCCGCGGGCAGATCAAGGACAGACGG T C lnc-DIAPH1-2 RNACentral:URS0000D591C7 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141512379..141512831 32194978 MeRIP-seq:(Medium) rs1475540731 Functional Loss SNV dbSNP153 33..33 33 - - - 109875 RMVar_ID_109875 Human_SNP_ID_253997619 m1A Human chr5 - 141573741 141573741 141573741 CCTTTGCCTGGGAGTGCTGGAATTCCCCCCCCACCTCCTCCCTTGCCTGGAGAAGCAGGAATGCC CCTTTGCCTGGGAGTGCTGGAATTCCCCCCCCCCCTCCTCCCTTGCCTGGAGAAGCAGGAATGCC T G DIAPH1 Ensembl:ENSG00000131504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141573698..141573878 26863196 MeRIP-seq:(Medium) rs1242514245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633742,Human_RBP_ID_4814110,Human_RBP_ID_5133877,Human_RBP_ID_9306715,Human_RBP_ID_17090116,Human_RBP_ID_21129299,Human_RBP_ID_26522561 Human_miRNA_ID_2028645,Human_miRNA_ID_2689182,Human_miRNA_ID_2692369 RMVar_hsa_circ_97418,RMVar_hsa_circ_119624,RMVar_hsa_circ_5992,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_76374,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_91511,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091,RMVar_hsa_circ_110882,RMVar_hsa_circ_127283,RMVar_hsa_circ_348962,RMVar_hsa_circ_119447,RMVar_hsa_circ_235092,RMVar_hsa_circ_235093,RMVar_hsa_circ_235094,RMVar_hsa_circ_95234,RMVar_hsa_circ_356274,RMVar_hsa_circ_235095,RMVar_hsa_circ_235096 109876 RMVar_ID_109876 Human_SNP_ID_253997639 m1A Human chr5 - 141573794 141573755 141573794 TCCCCCCACCTCCTCCTTTGCCTGGGAGTGCTAGAATCCCCCCACCACCACCTCCTTTGCCTGGG TCCCCCCACCTCCTCCTTTGCCTGGGAGTGCT_________________________________ CAGCACTCCCAGGCAAAGGAGGTGGTGGTGGGGGGATTCT C DIAPH1 Ensembl:ENSG00000131504 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:141573526..141573975;chr5:141573501..141573911 26863196 MeRIP-seq:(Medium) rs768124450 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_75176,Human_RBP_ID_165040,Human_RBP_ID_633744,Human_RBP_ID_946643,Human_RBP_ID_5133877,Human_RBP_ID_9307110,Human_RBP_ID_17090116,Human_RBP_ID_18956709,Human_RBP_ID_21129303,Human_RBP_ID_22296643,Human_RBP_ID_22459309,Human_RBP_ID_24087522,Human_RBP_ID_24536170,Human_RBP_ID_27075469 Human_miRNA_ID_2653038,Human_miRNA_ID_2754235 RMVar_hsa_circ_97418,RMVar_hsa_circ_119624,RMVar_hsa_circ_5992,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_76374,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_91511,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091,RMVar_hsa_circ_110882,RMVar_hsa_circ_127283,RMVar_hsa_circ_348962,RMVar_hsa_circ_119447,RMVar_hsa_circ_235092,RMVar_hsa_circ_235093,RMVar_hsa_circ_235094,RMVar_hsa_circ_95234,RMVar_hsa_circ_356274,RMVar_hsa_circ_235095,RMVar_hsa_circ_235096 109877 RMVar_ID_109877 Human_SNP_ID_253997669 m1A Human chr5 - 141573794 141573794 141573794 TCCCCCCACCTCCTCCTTTGCCTGGGAGTGCTAGAATCCCCCCACCACCACCTCCTTTGCCTGGG TCCCCCCACCTCCTCCTTTGCCTGGGAGTGCTGGAATCCCCCCACCACCACCTCCTTTGCCTGGG T C DIAPH1 Ensembl:ENSG00000131504 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:141573526..141573975;chr5:141573501..141573911 26863196 MeRIP-seq:(Medium) rs1461203802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75176,Human_RBP_ID_165040,Human_RBP_ID_633744,Human_RBP_ID_946643,Human_RBP_ID_5133877,Human_RBP_ID_9307110,Human_RBP_ID_17090116,Human_RBP_ID_18956709,Human_RBP_ID_21129303,Human_RBP_ID_22296643,Human_RBP_ID_22459309,Human_RBP_ID_24087522,Human_RBP_ID_24536170,Human_RBP_ID_27075469 Human_miRNA_ID_2653038,Human_miRNA_ID_2754235 RMVar_hsa_circ_97418,RMVar_hsa_circ_119624,RMVar_hsa_circ_5992,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_76374,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_91511,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091,RMVar_hsa_circ_110882,RMVar_hsa_circ_127283,RMVar_hsa_circ_348962,RMVar_hsa_circ_119447,RMVar_hsa_circ_235092,RMVar_hsa_circ_235093,RMVar_hsa_circ_235094,RMVar_hsa_circ_95234,RMVar_hsa_circ_356274,RMVar_hsa_circ_235095,RMVar_hsa_circ_235096 109878 RMVar_ID_109878 Human_SNP_ID_253997862 m1A Human chr5 + 141574105 141574105 141574105 CAGAGTCACCAGGTAAAGGAGGGGCAGGGGGAACAGGAGCACGACTAGGAACAGAAGGAGGTACA CAGAGTCACCAGGTAAAGGAGGGGCAGGGGGAGCAGGAGCACGACTAGGAACAGAAGGAGGTACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:141574019..141574148 26863196 MeRIP-seq:(Medium) rs1392252591 Functional Loss SNV dbSNP153 33..33 33 - - - 109879 RMVar_ID_109879 Human_SNP_ID_254008930 m1A Human chr5 - 141618859 141618857 141618860 GGGGCCCGGCCGCGGGACCCGGGACAAGAAGAAGGGCCGGAGCCCAGATGAGCTGCCCTCGGCGG GGGGCCCGGCCGCGGGACCCGGGACAAGAAG___GGCCGGAGCCCAGATGAGCTGCCCTCGGCGG CCTT C DIAPH1 Ensembl:ENSG00000131504 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:141618552..141619000 26863196 MeRIP-seq:(Medium) rs1199493968 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4845399,Human_RBP_ID_8893745,Human_RBP_ID_9306731,Human_RBP_ID_9335765,Human_RBP_ID_23050172,Human_RBP_ID_23120206,Human_RBP_ID_24548270 Human_Splice_Rec_701679,Human_Splice_Rec_701727,Human_Splice_Rec_701777,Human_Splice_Rec_701821,Human_Splice_Rec_701863,Human_Splice_Rec_701915,Human_Splice_Rec_702013 Human_miRNA_ID_2553142 RMVar_hsa_circ_85703,RMVar_hsa_circ_235098,RMVar_hsa_circ_94492,RMVar_hsa_circ_235104 109880 RMVar_ID_109880 Human_SNP_ID_254008952 m1A Human chr5 + 141618913 141618913 141618913 GGCCGGGCCCCAGGCTCCCGCCGGGCGGCTCCATGTCCCGGTTCACGCTGGCCGGCGACCCCGCG GGCCGGGCCCCAGGCTCCCGCCGGGCGGCTCCGTGTCCCGGTTCACGCTGGCCGGCGACCCCGCG A G AC008781.1 Ensembl:ENSG00000228737 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:141618801..141619000 26863410 MeRIP-seq:(Medium) rs1216396633 Functional Loss SNV dbSNP153 33..33 33 - - - 109881 RMVar_ID_109881 Human_SNP_ID_254008977 m1A Human chr5 + 141618938 141618938 141618938 CGGCTCCATGTCCCGGTTCACGCTGGCCGGCGACCCCGCGCCTACGCCGCTCCCGCCTGGCAGCT CGGCTCCATGTCCCGGTTCACGCTGGCCGGCGCCCCCGCGCCTACGCCGCTCCCGCCTGGCAGCT A C AC008781.1 Ensembl:ENSG00000228737 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:141618758..141619090;chr5:141618776..141619000;chr5:141618846..141619000;chr5:141618858..141619000;chr5:141618358..141625866;chr5:141618729..141619110;chr5:141618757..141619084 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs1282427345 Functional Loss SNV dbSNP153 33..33 33 - - - 109882 RMVar_ID_109882 Human_SNP_ID_254012683 m1A Human chr5 - 141634402 141634402 141634402 TCAGATGAAAGATGGTTGGAGGGTGAGGGGAGAAGTATAGCAGGCAGTAGGGACAAGTGCTAAGG TCAGATGAAAGATGGTTGGAGGGTGAGGGGAGGAGTATAGCAGGCAGTAGGGACAAGTGCTAAGG T C HDAC3 Ensembl:ENSG00000171720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141634270..141634526 26863196 MeRIP-seq:(Medium) rs534648594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633780,Human_RBP_ID_839633,Human_RBP_ID_7396085,Human_RBP_ID_15330794 RMVar_hsa_circ_88747,RMVar_hsa_circ_235108 109883 RMVar_ID_109883 Human_SNP_ID_254013133 m1A Human chr5 + 141636442 141636442 141636442 GGTACTCCTGGTGACTTCTATCCAGCTCCCCGATACTCTAGGGGCGGGTCGCACTTCATGCACTC GGTACTCCTGGTGACTTCTATCCAGCTCCCCGGTACTCTAGGGGCGGGTCGCACTTCATGCACTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:141636439..141636538 26863196 MeRIP-seq:(Medium) rs116972968 Functional Loss SNV dbSNP153 33..33 33 - - - 109884 RMVar_ID_109884 Human_SNP_ID_254013272 m1A Human chr5 - 141636781 141636781 141636781 CGGGGCCTGCTCCCGCCGGCACCATGGCCAAGACCGTGGCCTATTTCTACGACCCCGACGTGGGC CGGGGCCTGCTCCCGCCGGCACCATGGCCAAGGCCGTGGCCTATTTCTACGACCCCGACGTGGGC T C HDAC3 Ensembl:ENSG00000171720 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:141636576..141636875 26863410 MeRIP-seq:(Medium) rs1217514601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250382,Human_RBP_ID_4846050,Human_RBP_ID_18425024 Human_Splice_Rec_702067,Human_Splice_Rec_702143,Human_Splice_Rec_702159,Human_Splice_Rec_702179,Human_Splice_Rec_702195 RMVar_hsa_circ_88747,RMVar_hsa_circ_235108 109885 RMVar_ID_109885 Human_SNP_ID_254013281 m1A Human chr5 - 141636793 141636793 141636793 GCGGCGGAGGTGCGGGGCCTGCTCCCGCCGGCACCATGGCCAAGACCGTGGCCTATTTCTACGAC GCGGCGGAGGTGCGGGGCCTGCTCCCGCCGGCGCCATGGCCAAGACCGTGGCCTATTTCTACGAC T C HDAC3 Ensembl:ENSG00000171720 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:141636642..141636799 26863196 MeRIP-seq:(Medium) rs1322996288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250382,Human_RBP_ID_4814285,Human_RBP_ID_18425024 Human_Splice_Rec_702067,Human_Splice_Rec_702143,Human_Splice_Rec_702159,Human_Splice_Rec_702179,Human_Splice_Rec_702195 RMVar_hsa_circ_88747,RMVar_hsa_circ_235108 109886 RMVar_ID_109886 Human_SNP_ID_254013320 m1A Human chr5 + 141636815 141636815 141636815 TTGGCCATGGTGCCGGCGGGAGCAGGCCCCGCACCTCCGCCGCCCGCCGCCCGCGGCCGCCGCCA TTGGCCATGGTGCCGGCGGGAGCAGGCCCCGCCCCTCCGCCGCCCGCCGCCCGCGGCCGCCGCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141636742..141636850 26863196 MeRIP-seq:(Medium) rs768403725 Functional Loss SNV dbSNP153 33..33 33 - - - 109887 RMVar_ID_109887 Human_SNP_ID_254013574 m1A Human chr5 + 141637516 141637516 141637516 GATCTCCCTGACCCAGGGCCGGAGTTGCCCGGAGCCTGCCACCGCTCTCAGCCAGCCCGCATCCT GATCTCCCTGACCCAGGGCCGGAGTTGCCCGGGGCCTGCCACCGCTCTCAGCCAGCCCGCATCCT A G RELL2 Ensembl:ENSG00000164620 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141637466..141637608 26863196 MeRIP-seq:(Medium) rs968647226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8605317,Human_RBP_ID_22100522 109888 RMVar_ID_109888 Human_SNP_ID_254013655 m1A Human chr5 + 141637787 141637787 141637787 CAGGTGGTCAGGGTGGGAGAAACCAAAAAGGGAGAGGGGTGCGGGAGTACTGAGAGGAAGGGGCT CAGGTGGTCAGGGTGGGAGAAACCAAAAAGGGGGAGGGGTGCGGGAGTACTGAGAGGAAGGGGCT A G RELL2 Ensembl:ENSG00000164620 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141637747..141637903 26863196 MeRIP-seq:(Medium) rs1268489710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19124795 109889 RMVar_ID_109889 Human_SNP_ID_254015801 m1A Human chr5 - 141644692 141644692 141644692 AGTCTAATATCTGTTCACATTGCTGGGTGAGCAGGCTCGGAACCAGCACGGCGAGGTAGGCTTTG AGTCTAATATCTGTTCACATTGCTGGGTGAGCGGGCTCGGAACCAGCACGGCGAGGTAGGCTTTG T C FCHSD1 Ensembl:ENSG00000197948 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:141644677..141644881 26863196 MeRIP-seq:(Medium) rs199646898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269009 109890 RMVar_ID_109890 Human_SNP_ID_254015863 m1A Human chr5 - 141644852 141644852 141644852 AGGGAGATGCTGACGAATGGGTCAAGGTGGGTATGGGACCCCGGGCTCTGACCTTGGGTTGGGGG AGGGAGATGCTGACGAATGGGTCAAGGTGGGTTTGGGACCCCGGGCTCTGACCTTGGGTTGGGGG T A FCHSD1 Ensembl:ENSG00000197948 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:141644847..141644979 26863196 MeRIP-seq:(Medium) rs764758017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5395752 Human_Splice_Rec_702296,Human_Splice_Rec_702318,Human_Splice_Rec_702352,Human_Splice_Rec_702386,Human_Splice_Rec_702408 RMVar_hsa_circ_269009 109891 RMVar_ID_109891 Human_SNP_ID_254015933 m1A Human chr5 + 141645049 141645049 141645049 TACCTGATAGCGAAATACCACGTGTGCAGGGCAGGGGAGGGCCCTCGTGGCCAGGGCTTGGGGGG TACCTGATAGCGAAATACCACGTGTGCAGGGCGGGGGAGGGCCCTCGTGGCCAGGGCTTGGGGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141643020..141646201 32194978 MeRIP-seq:(Medium) rs746392666 Functional Loss SNV dbSNP153 33..33 33 - - - 109892 RMVar_ID_109892 Human_SNP_ID_254016127 m1A Human chr5 + 141645834 141645834 141645834 GCCTCACTGAGCCGCCGCTCCTGCTCCACCTCATCCTGGGCCTGGGTCATGGCTGGCTTCAGCCA GCCTCACTGAGCCGCCGCTCCTGCTCCACCTCCTCCTGGGCCTGGGTCATGGCTGGCTTCAGCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141645769..141645882 26863196 MeRIP-seq:(Medium) rs1281758374 Functional Loss SNV dbSNP153 33..33 33 - - - 109893 RMVar_ID_109893 Human_SNP_ID_254016392 m1A Human chr5 - 141646668 141646668 141646668 CAGAAGGCGTGGCTGGCAAGAGTGGCCTGGAGAAAGAGGTTCAGCGCTTGACCAGCCGAGCTGCC CAGAAGGCGTGGCTGGCAAGAGTGGCCTGGAGGAAGAGGTTCAGCGCTTGACCAGCCGAGCTGCC T C FCHSD1 Ensembl:ENSG00000197948 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141646498..141647576 32194978 MeRIP-seq:(Medium) rs902469668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967492,Human_RBP_ID_19015998 Human_Splice_Rec_702288,Human_Splice_Rec_702289,Human_Splice_Rec_702312,Human_Splice_Rec_702344,Human_Splice_Rec_702345,Human_Splice_Rec_702380,Human_Splice_Rec_702381,Human_Splice_Rec_702414,Human_Splice_Rec_702418 RMVar_hsa_circ_65291,RMVar_hsa_circ_102406,RMVar_hsa_circ_269009,RMVar_hsa_circ_235118 109894 RMVar_ID_109894 Human_SNP_ID_254025661 m1A Human chr5 - 141680098 141680091 141680098 CCTCGGGGGACCAGGAGTGTCCAGGAGCCCAGAGCCCAGCCCAAGGCCTCCTCCTCTCCCCACTT CCTCGGGGGACCAGGAGTGTCCAGGAGCCCAG_______CCCAAGGCCTCCTCCTCTCCCCACTT GCTGGGCT G ARAP3 Ensembl:ENSG00000120318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141680056..141680125 26863196 MeRIP-seq:(Medium) rs1457132359 Functional Loss DEL dbSNP153 33..39 33 - - - 109895 RMVar_ID_109895 Human_SNP_ID_254025664 m1A Human chr5 - 141680098 141680098 141680098 CCTCGGGGGACCAGGAGTGTCCAGGAGCCCAGAGCCCAGCCCAAGGCCTCCTCCTCTCCCCACTT CCTCGGGGGACCAGGAGTGTCCAGGAGCCCAGTGCCCAGCCCAAGGCCTCCTCCTCTCCCCACTT T A ARAP3 Ensembl:ENSG00000120318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141680056..141680125 26863196 MeRIP-seq:(Medium) rs1350436620 Functional Loss SNV dbSNP153 33..33 33 - - - 109896 RMVar_ID_109896 Human_SNP_ID_254085867 m1A Human chr5 + 141923936 141923936 141923936 GCTTTCGGCTGCGAGCTCTCTGTGGTGCTGGCAGCGACATGTGGCGCCTCCCGGGACTCCTGGGC GCTTTCGGCTGCGAGCTCTCTGTGGTGCTGGCGGCGACATGTGGCGCCTCCCGGGACTCCTGGGC A G DELE1 Ensembl:ENSG00000081791 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141923888..141924616 26863196 MeRIP-seq:(Medium) rs921828359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_633794,Human_RBP_ID_787474,Human_RBP_ID_4846054,Human_RBP_ID_18425192 Human_Splice_Rec_702761,Human_Splice_Rec_702785,Human_Splice_Rec_702807 RMVar_hsa_circ_89065,RMVar_hsa_circ_235134 109897 RMVar_ID_109897 Human_SNP_ID_254085871 m1A Human chr5 - 141923945 141923945 141923945 CTTACCTCGGCCCAGGAGTCCCGGGAGGCGCCACATGTCGCTGCCAGCACCACAGAGAGCTCGCA CTTACCTCGGCCCAGGAGTCCCGGGAGGCGCCGCATGTCGCTGCCAGCACCACAGAGAGCTCGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141923896..141924249 26863196 MeRIP-seq:(Medium) rs1458534603 Functional Loss SNV dbSNP153 33..33 33 - - - 109898 RMVar_ID_109898 Human_SNP_ID_254086115 m1A Human chr5 + 141924694 141924694 141924694 CCACTTTGCTGGTTCCTGTGCCTAACCTCGACAGGTAAGATACTGCCATTTTACCACTCATTTCC CCACTTTGCTGGTTCCTGTGCCTAACCTCGACCGGTAAGATACTGCCATTTTACCACTCATTTCC A C DELE1 Ensembl:ENSG00000081791 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:141924676..141924700 32194978 MeRIP-seq:(Medium) rs754651831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19016009 Human_Splice_Rec_702763,Human_Splice_Rec_702787,Human_Splice_Rec_702809 RMVar_hsa_circ_89065,RMVar_hsa_circ_105400,RMVar_hsa_circ_235134,RMVar_hsa_circ_369791,RMVar_hsa_circ_235135,RMVar_hsa_circ_235136 109899 RMVar_ID_109899 Human_SNP_ID_254086385 m1A Human chr5 + 141925480 141925480 141925480 GGTCCCATGGATGGAAGGATGCCTTCCAATGGATGTCTTCCCGTGTCTCCCCGAACACCCTATGG GGTCCCATGGATGGAAGGATGCCTTCCAATGGGTGTCTTCCCGTGTCTCCCCGAACACCCTATGG A G DELE1 Ensembl:ENSG00000081791 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141925429..141928300 32194978 MeRIP-seq:(Medium) rs765737948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967504,Human_RBP_ID_19016011,Human_RBP_ID_23040276 Human_Splice_Rec_702764,Human_Splice_Rec_702765,Human_Splice_Rec_702788,Human_Splice_Rec_702789,Human_Splice_Rec_702810,Human_Splice_Rec_702811 Human_miRNA_ID_2480662,Human_miRNA_ID_2951550,Human_miRNA_ID_3057101 RMVar_hsa_circ_89065,RMVar_hsa_circ_105400,RMVar_hsa_circ_235134,RMVar_hsa_circ_235136 109900 RMVar_ID_109900 Human_SNP_ID_254086386 m1A Human chr5 + 141925480 141925480 141925480 GGTCCCATGGATGGAAGGATGCCTTCCAATGGATGTCTTCCCGTGTCTCCCCGAACACCCTATGG GGTCCCATGGATGGAAGGATGCCTTCCAATGGTTGTCTTCCCGTGTCTCCCCGAACACCCTATGG A T DELE1 Ensembl:ENSG00000081791 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:141925429..141928300 32194978 MeRIP-seq:(Medium) rs765737948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967504,Human_RBP_ID_19016011,Human_RBP_ID_23040276 Human_Splice_Rec_702764,Human_Splice_Rec_702765,Human_Splice_Rec_702788,Human_Splice_Rec_702789,Human_Splice_Rec_702810,Human_Splice_Rec_702811 Human_miRNA_ID_2480662,Human_miRNA_ID_2951550,Human_miRNA_ID_3057101 RMVar_hsa_circ_89065,RMVar_hsa_circ_105400,RMVar_hsa_circ_235134,RMVar_hsa_circ_235136 109901 RMVar_ID_109901 Human_SNP_ID_254087394 m1A Human chr5 + 141929558 141929558 141929558 AGGTGTGAGCCATCGCGCCTGGCCCAGACCTGACTACTCTTGCTGGCTCTTTCCAGCACTGCGAC AGGTGTGAGCCATCGCGCCTGGCCCAGACCTGTCTACTCTTGCTGGCTCTTTCCAGCACTGCGAC A T DELE1 Ensembl:ENSG00000081791 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141929555..141929668 26863196 MeRIP-seq:(Medium) rs777238262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37762,RMVar_hsa_circ_105400,RMVar_hsa_circ_235136 109902 RMVar_ID_109902 Human_SNP_ID_254097572 m1A Human chr5 + 141969181 141969181 141969181 GCCTGGTCGGCTGGCGGCGGTGAGTGGGCCCCAGGCAAGGGCGGAGGGCGGAACTTTGGGGTTCG GCCTGGTCGGCTGGCGGCGGTGAGTGGGCCCCTGGCAAGGGCGGAGGGCGGAACTTTGGGGTTCG A T RNF14 Ensembl:ENSG00000013561 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:141969179..141969365 26863196 MeRIP-seq:(Medium) rs1157323958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_702981 109903 RMVar_ID_109903 Human_SNP_ID_254108098 m1A Human chr5 - 142012859 142012859 142012859 TCACACATTTTCCAGGAGGGATCGGAGGGGCGATGGGGTGGTAATGGGGGTGGGGGACACGCTGT TCACACATTTTCCAGGAGGGATCGGAGGGGCGCTGGGGTGGTAATGGGGGTGGGGGACACGCTGT T G GNPDA1 Ensembl:ENSG00000113552 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:142012851..142013007 26863196 MeRIP-seq:(Medium) rs1183806479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19128167 109904 RMVar_ID_109904 Human_SNP_ID_254131837 m1A Human chr5 + 142108874 142108874 142108874 CGGGAGCGGCGGCGGCCATCGAGACCCACCCAAGGCGCGTCCCCCTCGGCCTCCCAGCGCTCCCA CGGGAGCGGCGGCGGCCATCGAGACCCACCCAGGGCGCGTCCCCCTCGGCCTCCCAGCGCTCCCA A G NDFIP1 Ensembl:ENSG00000131507 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:142108776..142109000 26863196 MeRIP-seq:(Medium) rs1172153014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78124,Human_RBP_ID_4814555,Human_RBP_ID_5508999,Human_RBP_ID_27075553 109905 RMVar_ID_109905 Human_SNP_ID_254131854 m1A Human chr5 + 142108913 142108913 142108913 TCCCCCTCGGCCTCCCAGCGCTCCCAAGCCGCAGCGGCCGCGCCCCTTCAGCTAGCTCGCTCGCT TCCCCCTCGGCCTCCCAGCGCTCCCAAGCCGCTGCGGCCGCGCCCCTTCAGCTAGCTCGCTCGCT A T NDFIP1 Ensembl:ENSG00000131507 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:142108776..142109077 26863196 MeRIP-seq:(Medium) rs6862280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4845404 109906 RMVar_ID_109906 Human_SNP_ID_254293234 m1A Human chr5 + 142770468 142770464 142770468 GCTAGCGAAGGAGGCGGGGAGGCGGCGTCTGCACTCGCTCGCCCGCTCGCTCGCTTCCCGGCGCC GCTAGCGAAGGAGGCGGGGAGGCGGCGTC____CTCGCTCGCCCGCTCGCTCGCTTCCCGGCGCC CTGCA C ARHGAP26 Ensembl:ENSG00000145819 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:142770427..142770634 26863196 MeRIP-seq:(Medium) rs202198182 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_250763,Human_RBP_ID_18425193 109907 RMVar_ID_109907 Human_SNP_ID_254293238 m1A Human chr5 - 142770470 142770466 142770470 GCGGCGCCGGGAAGCGAGCGAGCGGGCGAGCGAGTGCAGACGCCGCCTCCCCGCCTCCTTCGCTA GCGGCGCCGGGAAGCGAGCGAGCGGGCGAGCG____CAGACGCCGCCTCCCCGCCTCCTTCGCTA GCACT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:142770433..142770539 26863196 MeRIP-seq:(Medium) rs146003189 Functional Loss DEL dbSNP153 33..36 33 - - - GWAS_ID_15318 109908 RMVar_ID_109908 Human_SNP_ID_254293248 m1A Human chr5 - 142770486 142770486 142770486 GCAGCGCGGACCCGCAGCGGCGCCGGGAAGCGAGCGAGCGGGCGAGCGAGTGCAGACGCCGCCTC GCAGCGCGGACCCGCAGCGGCGCCGGGAAGCGGGCGAGCGGGCGAGCGAGTGCAGACGCCGCCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:142770443..142770571 26863196 MeRIP-seq:(Medium) rs1435493172 Functional Loss SNV dbSNP153 33..33 33 - - - 109909 RMVar_ID_109909 Human_SNP_ID_254355365 m1A Human chr5 - 143031398 143031398 143031398 TCATCATCACCATCCTGGTCCCTACCTCAATCATCTGTTGCCAGGATGACTGCATTAACCTCCTG TCATCATCACCATCCTGGTCCCTACCTCAATCGTCTGTTGCCAGGATGACTGCATTAACCTCCTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:143031395..143031475 26863196 MeRIP-seq:(Medium) rs554673956 Functional Loss SNV dbSNP153 33..33 33 - - - 109910 RMVar_ID_109910 Human_SNP_ID_254416471 m1A Human chr5 - 143291003 143291003 143291003 CCATTGGGGGAAGAGAATACCTAAGAAAAACAATCCAAAAGAATGAAAGACATGAGAGGAGGGAG CCATTGGGGGAAGAGAATACCTAAGAAAAACAGTCCAAAAGAATGAAAGACATGAGAGGAGGGAG T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:143290954..143291030 26863196 MeRIP-seq:(Medium) rs887409015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_98442,RMVar_hsa_circ_235196,RMVar_hsa_circ_68464 109911 RMVar_ID_109911 Human_SNP_ID_254441781 m1A Human chr5 + 143400851 143400851 143400851 TAATGATTCTTTGGAGTCCATCAGTGAATATCAACTACAAAACAAAAAACAAAAACGGGGGGAAA TAATGATTCTTTGGAGTCCATCAGTGAATATCGACTACAAAACAAAAAACAAAAACGGGGGGAAA A G KU921432 RNACentral:URS0000A3C9C3 Other intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:143400801..143400875 26863196 MeRIP-seq:(Medium) rs957389964 Functional Loss SNV dbSNP153 33..33 33 - - - 109912 RMVar_ID_109912 Human_SNP_ID_254442582 m1A Human chr5 - 143403420 143403420 143403420 AACCTCGACCCGCGGAGCCCGGCGCGGGGCGGAGGGCTGGCTTGTCAGCTGGGCAATGGGAGACT AACCTCGACCCGCGGAGCCCGGCGCGGGGCGGGGGGCTGGCTTGTCAGCTGGGCAATGGGAGACT T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:143403376..143403525;chr5:143403376..143403872;chr5:143403376..143403687 26863196 MeRIP-seq:(Medium) rs914191753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846065 RMVar_hsa_circ_127842,RMVar_hsa_circ_235201 109913 RMVar_ID_109913 Human_SNP_ID_254442607 m1A Human chr5 - 143403452 143403452 143403452 AGCTGGGACCGGGACGGGGCACGCGCGCCCGGAACCTCGACCCGCGGAGCCCGGCGCGGGGCGGA AGCTGGGACCGGGACGGGGCACGCGCGCCCGGCACCTCGACCCGCGGAGCCCGGCGCGGGGCGGA T G NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:143403404..143403735 26863196 MeRIP-seq:(Medium) rs1365143692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4846763,Human_RBP_ID_8943857 RMVar_hsa_circ_127842,RMVar_hsa_circ_235201 109914 RMVar_ID_109914 Human_SNP_ID_254442628 m1A Human chr5 - 143403502 143403488 143403503 GGACGGATTCTGTGGGTGGAAGGAGACGCCGCAGCCGGAGCGGCCGAAGCAGCTGGGACCGGGAC GGACGGATTCTGTGGGTGGAAGGAGACGCCG_______________AAGCAGCTGGGACCGGGAC TCGGCCGCTCCGGCTG T NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:143403411..143403621 26863196 MeRIP-seq:(Medium) rs1230254260 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_839206,Human_RBP_ID_4846763,Human_RBP_ID_8943857,Human_RBP_ID_9335392 RMVar_hsa_circ_127842,RMVar_hsa_circ_235201 109915 RMVar_ID_109915 Human_SNP_ID_254442634 m1A Human chr5 - 143403502 143403502 143403502 GGACGGATTCTGTGGGTGGAAGGAGACGCCGCAGCCGGAGCGGCCGAAGCAGCTGGGACCGGGAC GGACGGATTCTGTGGGTGGAAGGAGACGCCGCCGCCGGAGCGGCCGAAGCAGCTGGGACCGGGAC T G NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:143403411..143403621 26863196 MeRIP-seq:(Medium) rs1314297554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_839206,Human_RBP_ID_4846763,Human_RBP_ID_8943857,Human_RBP_ID_9335392 RMVar_hsa_circ_127842,RMVar_hsa_circ_235201 109916 RMVar_ID_109916 Human_SNP_ID_254442838 m1A Human chr5 + 143403970 143403970 143403970 CCCAACTCCCCAGGAAAAAGGGTGGCGGCGGCAGCGGCGGGGGCCGACCTGGTCTCTCTGGGGCG CCCAACTCCCCAGGAAAAAGGGTGGCGGCGGCTGCGGCGGGGGCCGACCTGGTCTCTCTGGGGCG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:143403962..143404141 26863196 MeRIP-seq:(Medium) rs1176286904 Functional Loss SNV dbSNP153 33..33 33 - - - 109917 RMVar_ID_109917 Human_SNP_ID_254634244 m1A Human chr5 + 144170589 144170589 144170589 GGCAAAGGCAGTAGCTTCACTAATCCCAAACAACCCCCAAACTCTGTTTCAGACCCTGAACCAGC GGCAAAGGCAGTAGCTTCACTAATCCCAAACAGCCCCCAAACTCTGTTTCAGACCCTGAACCAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:144170496..144170602 26863196 MeRIP-seq:(Medium) rs1347557412 Functional Loss SNV dbSNP153 33..33 33 - - - 109918 RMVar_ID_109918 Human_SNP_ID_255062961 m1A Human chr5 + 145835276 145835276 145835276 ACCCCCATCCCCGCGCGCCGCGGGCCCCGCGCACCGGCCACGCCTCCGCGAGCTCAGAGCTGCCC ACCCCCATCCCCGCGCGCCGCGGGCCCCGCGCGCCGGCCACGCCTCCGCGAGCTCAGAGCTGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:145835230..145835332 26863196 MeRIP-seq:(Medium) rs1191902168 Functional Loss SNV dbSNP153 33..33 33 - - - 109919 RMVar_ID_109919 Human_SNP_ID_255062978 m1A Human chr5 + 145835321 145835321 145835321 CCGCGAGCTCAGAGCTGCCCAGGGCTCCGCAGAGGCCCGGAGGCGCCCACACTCGGACAGCCACA CCGCGAGCTCAGAGCTGCCCAGGGCTCCGCAGGGGCCCGGAGGCGCCCACACTCGGACAGCCACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:145835223..145835335 26863196 MeRIP-seq:(Medium) rs1214821164 Functional Loss SNV dbSNP153 33..33 33 - - - 109920 RMVar_ID_109920 Human_SNP_ID_255133940 m1A Human chr5 - 146129029 146129029 146129029 ATACACTCCTCACAGTATCTTATGGAAGTAACACATGACCTTAGACTACGACTCAAGAACTATAT ATACACTCCTCACAGTATCTTATGGAAGTAACGCATGACCTTAGACTACGACTCAAGAACTATAT T C LARS1 Ensembl:ENSG00000133706 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146128937..146129076 26863196 MeRIP-seq:(Medium) rs1217585819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75290,Human_RBP_ID_1989588,Human_RBP_ID_8606301,Human_RBP_ID_8885884,Human_RBP_ID_9306740,Human_RBP_ID_23040715,Human_RBP_ID_24089118 Human_Splice_Rec_704258,Human_Splice_Rec_704259,Human_Splice_Rec_704286,Human_Splice_Rec_704287,Human_Splice_Rec_704312,Human_Splice_Rec_704313,Human_Splice_Rec_704370,Human_Splice_Rec_704371,Human_Splice_Rec_704430,Human_Splice_Rec_704431,Human_Splice_Rec_704488,Human_Splice_Rec_704489,Human_Splice_Rec_704548,Human_Splice_Rec_704549,Human_Splice_Rec_704608,Human_Splice_Rec_704609,Human_Splice_Rec_704670,Human_Splice_Rec_704671,Human_Splice_Rec_704730,Human_Splice_Rec_704731,Human_Splice_Rec_704790,Human_Splice_Rec_704791,Human_Splice_Rec_704850,Human_Splice_Rec_704851,Human_Splice_Rec_704912,Human_Splice_Rec_704913,Human_Splice_Rec_704974,Human_Splice_Rec_704975,Human_Splice_Rec_705036,Human_Splice_Rec_705037,Human_Splice_Rec_705098,Human_Splice_Rec_705099,Human_Splice_Rec_705160,Human_Splice_Rec_705161,Human_Splice_Rec_705222,Human_Splice_Rec_705223,Human_Splice_Rec_705254,Human_Splice_Rec_705255,Human_Splice_Rec_705284,Human_Splice_Rec_705285,Human_Splice_Rec_705344,Human_Splice_Rec_705345,Human_Splice_Rec_705406,Human_Splice_Rec_705407,Human_Splice_Rec_705422,Human_Splice_Rec_705423 RMVar_hsa_circ_59893,RMVar_hsa_circ_65155,RMVar_hsa_circ_24770,RMVar_hsa_circ_53281,RMVar_hsa_circ_376203,RMVar_hsa_circ_40070,RMVar_hsa_circ_265072,RMVar_hsa_circ_235233 109921 RMVar_ID_109921 Human_SNP_ID_255134987 m1A Human chr5 - 146132949 146132949 146132949 AGAGTGGGTGAAAGAAATGGTTGCCAACTGGGACAGCCTAAGAAGTGGTCCTGCCAGCACTTTCA AGAGTGGGTGAAAGAAATGGTTGCCAACTGGGGCAGCCTAAGAAGTGGTCCTGCCAGCACTTTCA T C LARS1 Ensembl:ENSG00000133706 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:146132624..146135664 32194978 MeRIP-seq:(Medium) rs751432978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1989599,Human_RBP_ID_3968293,Human_RBP_ID_4851064,Human_RBP_ID_8606308,Human_RBP_ID_8885893,Human_RBP_ID_9171639,Human_RBP_ID_18835335,Human_RBP_ID_24089134,Human_RBP_ID_25868284 Human_Splice_Rec_704255,Human_Splice_Rec_704281,Human_Splice_Rec_704365,Human_Splice_Rec_704425,Human_Splice_Rec_704483,Human_Splice_Rec_704543,Human_Splice_Rec_704603,Human_Splice_Rec_704665,Human_Splice_Rec_704727,Human_Splice_Rec_704787,Human_Splice_Rec_704845,Human_Splice_Rec_704907,Human_Splice_Rec_704969,Human_Splice_Rec_705031,Human_Splice_Rec_705093,Human_Splice_Rec_705155,Human_Splice_Rec_705217,Human_Splice_Rec_705249,Human_Splice_Rec_705279,Human_Splice_Rec_705339,Human_Splice_Rec_705401,Human_Splice_Rec_705473 Human_miRNA_ID_169369 RMVar_hsa_circ_59893,RMVar_hsa_circ_65155,RMVar_hsa_circ_19216,RMVar_hsa_circ_24770,RMVar_hsa_circ_53281,RMVar_hsa_circ_376203,RMVar_hsa_circ_40070,RMVar_hsa_circ_265072,RMVar_hsa_circ_41222,RMVar_hsa_circ_109680,RMVar_hsa_circ_235233,RMVar_hsa_circ_100747,RMVar_hsa_circ_20383,RMVar_hsa_circ_235234,RMVar_hsa_circ_235235,RMVar_hsa_circ_235236 109922 RMVar_ID_109922 Human_SNP_ID_255137733 m1A Human chr5 + 146143492 146143492 146143492 AATAGGTGTGCAACTGTGTAAAATGCCATGTAAATAGTGGAGTCAGAAAGTGATTCAATCAGCCA AATAGGTGTGCAACTGTGTAAAATGCCATGTAGATAGTGGAGTCAGAAAGTGATTCAATCAGCCA A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:146143441..146144479 32194978 MeRIP-seq:(Medium) rs762293311 Functional Loss SNV dbSNP153 33..33 33 - - - 109923 RMVar_ID_109923 Human_SNP_ID_255141367 m1A Human chr5 + 146157755 146157755 146157755 CCTACCTTAATTTAGATGGGTATGGCTCAAGCACCTTCAATTTGAGTAAAGTATATTCCTGAGGT CCTACCTTAATTTAGATGGGTATGGCTCAAGCGCCTTCAATTTGAGTAAAGTATATTCCTGAGGT A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:146157750..146159462 32194978 MeRIP-seq:(Medium) rs775525280 Functional Loss SNV dbSNP153 33..33 33 - - - 109924 RMVar_ID_109924 Human_SNP_ID_255154129 m1A Human chr5 + 146203652 146203652 146203652 CCGGCCGGGGGAGTAGGTTGAAGTCTCCTAAGATGCCCGGTGGGCTGGGGCACCGGGAGCTGTGA CCGGCCGGGGGAGTAGGTTGAAGTCTCCTAAGTTGCCCGGTGGGCTGGGGCACCGGGAGCTGTGA A T RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:146203601..146203825;chr5:146203601..146203799;chr5:146203601..146203800 26863196 MeRIP-seq:(Medium) rs1297565543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_787503,Human_RBP_ID_4846071,Human_RBP_ID_9171672,Human_RBP_ID_9306757,Human_RBP_ID_18425028,Human_RBP_ID_18448294,Human_RBP_ID_23050357,Human_RBP_ID_24089303 RMVar_hsa_circ_121108,RMVar_hsa_circ_235260 109925 RMVar_ID_109925 Human_SNP_ID_255175244 m1A Human chr5 + 146286790 146286790 146286790 CGCTGGTTCGGCTGGTCTTTTTAAAAATTTTTATAACTCAGAATGTAAAAGGCTTTCACCTATTG CGCTGGTTCGGCTGGTCTTTTTAAAAATTTTTCTAACTCAGAATGTAAAAGGCTTTCACCTATTG A C RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:146286739..146286840 32194978 MeRIP-seq:(Medium) rs914751404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74006,Human_RBP_ID_2906011,Human_RBP_ID_7401443,Human_RBP_ID_8133116,Human_RBP_ID_17412174,Human_RBP_ID_18058292,Human_RBP_ID_18354766,Human_RBP_ID_24089385,Human_RBP_ID_24504147,Human_RBP_ID_27736372 Human_miRNA_ID_857979,Human_miRNA_ID_996499,Human_miRNA_ID_1275957 RMVar_hsa_circ_121973,RMVar_hsa_circ_235261,RMVar_hsa_circ_267781,RMVar_hsa_circ_107671,RMVar_hsa_circ_235299 109926 RMVar_ID_109926 Human_SNP_ID_255175778 m1A Human chr5 + 146289162 146289162 146289162 TGGAAAAAAAAAAGAAAAAAGATGAAAGTATTACAAATTTAAAAGAATTTGGAAAATTTATGAAC TGGAAAAAAAAAAGAAAAAAGATGAAAGTATTGCAAATTTAAAAGAATTTGGAAAATTTATGAAC A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17687490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22402657 GWAS_ID_15319,GWAS_ID_15320,GWAS_ID_15321,GWAS_ID_15322 RMVar_hsa_circ_121973,RMVar_hsa_circ_235261,RMVar_hsa_circ_267781,RMVar_hsa_circ_107671,RMVar_hsa_circ_235299 109927 RMVar_ID_109927 Human_SNP_ID_255214762 m1A Human chr5 + 146447369 146447369 146447369 GCGGCCCTCTGTAATGGCGGAGCGTGGCGGGGACGGGGGCGAGAGTGAACGATTCAACCCGGGGG GCGGCCCTCTGTAATGGCGGAGCGTGGCGGGGGCGGGGGCGAGAGTGAACGATTCAACCCGGGGG A G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146447326..146447490 26863196 MeRIP-seq:(Medium) rs1039013282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12519,Human_RBP_ID_74816,Human_RBP_ID_249968,Human_RBP_ID_787674,Human_RBP_ID_8885994,Human_RBP_ID_9398494,Human_RBP_ID_18425029,Human_RBP_ID_18448303,Human_RBP_ID_19016042,Human_RBP_ID_27825983 Human_Splice_Rec_705721,Human_Splice_Rec_705741,Human_Splice_Rec_705783,Human_Splice_Rec_705823 RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300 109928 RMVar_ID_109928 Human_SNP_ID_255214788 m1A Human chr5 + 146447402 146447402 146447402 CGGGGGCGAGAGTGAACGATTCAACCCGGGGGAGCTCAGGTAAGGAACGCTGCCCTCCTTCACAT CGGGGGCGAGAGTGAACGATTCAACCCGGGGGGGCTCAGGTAAGGAACGCTGCCCTCCTTCACAT A G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr5:146447351..146447465;chr5:146447351..146447477 26863410,26863196 MeRIP-seq:(Medium) rs1342889602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12519,Human_RBP_ID_943070,Human_RBP_ID_2906100,Human_RBP_ID_3968317,Human_RBP_ID_5426962,Human_RBP_ID_9398494,Human_RBP_ID_18041582,Human_RBP_ID_18425030,Human_RBP_ID_18448304,Human_RBP_ID_18835502,Human_RBP_ID_19016042,Human_RBP_ID_19126519,Human_RBP_ID_26351559,Human_RBP_ID_26827521,Human_RBP_ID_27825983 Human_Splice_Rec_705721,Human_Splice_Rec_705741,Human_Splice_Rec_705783,Human_Splice_Rec_705823 RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300 109929 RMVar_ID_109929 Human_SNP_ID_255214790 m1A Human chr5 - 146447405 146447405 146447405 GAGATGTGAAGGAGGGCAGCGTTCCTTACCTGAGCTCCCCCGGGTTGAATCGTTCACTCTCGCCC GAGATGTGAAGGAGGGCAGCGTTCCTTACCTGGGCTCCCCCGGGTTGAATCGTTCACTCTCGCCC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:146447326..146447541 26863196 MeRIP-seq:(Medium) rs774616410 Functional Loss SNV dbSNP153 33..33 33 - - - 109930 RMVar_ID_109930 Human_SNP_ID_255216845 m1A Human chr5 - 146455016 146455016 146455016 GGAAAGCAAGGAATAAATTTTTCTTTCTTAAAATTACAAAAATGTAGCTACTGATCTCTAATTAC GGAAAGCAAGGAATAAATTTTTCTTTCTTAAAGTTACAAAAATGTAGCTACTGATCTCTAATTAC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:146455014..146455320 26863196 MeRIP-seq:(Medium) rs532156989 Functional Loss SNV dbSNP153 33..33 33 - - - 109931 RMVar_ID_109931 Human_SNP_ID_255216878 m1A Human chr5 + 146455125 146455125 146455125 GCTCCCCCACCAAATGCAGTGATGCGAGGCCCACCACCTCTGATGCGACCTCCTCCACCTTTTGG GCTCCCCCACCAAATGCAGTGATGCGAGGCCCCCCACCTCTGATGCGACCTCCTCCACCTTTTGG A C TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:146455076..146455220 26863196 MeRIP-seq:(Medium) rs1561632818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1319989,Human_RBP_ID_1390540,Human_RBP_ID_4815678,Human_RBP_ID_18425031,Human_RBP_ID_18835506,Human_RBP_ID_24089444,Human_RBP_ID_26826701,Human_RBP_ID_27332597 Human_Splice_Rec_705722,Human_Splice_Rec_705742,Human_Splice_Rec_705784,Human_Splice_Rec_705824 RMVar_hsa_circ_12950,RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_366868,RMVar_hsa_circ_235300,RMVar_hsa_circ_306386,RMVar_hsa_circ_235303 109932 RMVar_ID_109932 Human_SNP_ID_255218047 m1A Human chr5 + 146459277 146459277 146459277 CACCTGCAGTATCCACTTCAACATCATCATCCACCCCTTCCTCTACCACTTCTACCACAACAACT CACCTGCAGTATCCACTTCAACATCATCATCCCCCCCTTCCTCTACCACTTCTACCACAACAACT A C TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146459226..146459376 26863196 MeRIP-seq:(Medium) rs747728427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74821,Human_RBP_ID_249969,Human_RBP_ID_2906108,Human_RBP_ID_8267416,Human_RBP_ID_9399563,Human_RBP_ID_17298625,Human_RBP_ID_17412185,Human_RBP_ID_17528068,Human_RBP_ID_18041589,Human_RBP_ID_18538728,Human_RBP_ID_18956738,Human_RBP_ID_27512539,Human_RBP_ID_27825988 Human_Splice_Rec_705727,Human_Splice_Rec_705747,Human_Splice_Rec_705789,Human_Splice_Rec_705829,Human_Splice_Rec_705867 Human_miRNA_ID_2384056,Human_miRNA_ID_3094393 RMVar_hsa_circ_12950,RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300,RMVar_hsa_circ_306386,RMVar_hsa_circ_97072,RMVar_hsa_circ_108113,RMVar_hsa_circ_235303,RMVar_hsa_circ_373132,RMVar_hsa_circ_235304,RMVar_hsa_circ_235305,RMVar_hsa_circ_235306 109933 RMVar_ID_109933 Human_SNP_ID_255218987 m1A Human chr5 - 146463582 146463580 146463583 ACACTAACTGTAGGCGTGGCAACTGAAACAGCAGAACTTGGGGTCTGATCTTGTGTTGTGGGTGC ACACTAACTGTAGGCGTGGCAACTGAAACAG___AACTTGGGGTCTGATCTTGTGTTGTGGGTGC TCTG T RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:146463551..146463844 26863196 MeRIP-seq:(Medium) rs764963678 Functional Loss DEL dbSNP153 32..34 33 - - - 109934 RMVar_ID_109934 Human_SNP_ID_255223117 m1A Human chr5 - 146480584 146480584 146480584 TTTACATTTTACCCAACTCTAGAGCACTGGCCAAGCTAATGCCTCTACTTCTTAGCAGTCTCTTT TTTACATTTTACCCAACTCTAGAGCACTGGCCTAGCTAATGCCTCTACTTCTTAGCAGTCTCTTT T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:146480539..146480745 26863196 MeRIP-seq:(Medium) rs1056894 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15323,GWAS_ID_15324 109935 RMVar_ID_109935 Human_SNP_ID_255223118 m1A Human chr5 - 146480584 146480584 146480584 TTTACATTTTACCCAACTCTAGAGCACTGGCCAAGCTAATGCCTCTACTTCTTAGCAGTCTCTTT TTTACATTTTACCCAACTCTAGAGCACTGGCCGAGCTAATGCCTCTACTTCTTAGCAGTCTCTTT T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:146480539..146480745 26863196 MeRIP-seq:(Medium) rs1056894 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15323,GWAS_ID_15324 109936 RMVar_ID_109936 Human_SNP_ID_255223653 m1A Human chr5 + 146482900 146482900 146482900 GCAACAGCCTTTTTCTTGGCTAATCTTATCATATTTAACTAAATGCCATTTTACTGTCCTTTTAA GCAACAGCCTTTTTCTTGGCTAATCTTATCATGTTTAACTAAATGCCATTTTACTGTCCTTTTAA A G TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3756502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17629963,Human_RBP_ID_24433690,Human_RBP_ID_25869724 GWAS_ID_15325 RMVar_hsa_circ_29859,RMVar_hsa_circ_101453,RMVar_hsa_circ_235300,RMVar_hsa_circ_33041,RMVar_hsa_circ_108113,RMVar_hsa_circ_235305,RMVar_hsa_circ_119316,RMVar_hsa_circ_339815,RMVar_hsa_circ_126626,RMVar_hsa_circ_115636,RMVar_hsa_circ_235307,RMVar_hsa_circ_235308,RMVar_hsa_circ_235309,RMVar_hsa_circ_50450,RMVar_hsa_circ_49040,RMVar_hsa_circ_371813,RMVar_hsa_circ_235310,RMVar_hsa_circ_73960,RMVar_hsa_circ_354539,RMVar_hsa_circ_52492,RMVar_hsa_circ_235313,RMVar_hsa_circ_305646,RMVar_hsa_circ_17533 109937 RMVar_ID_109937 Human_SNP_ID_255291532 m1A Human chr5 - 146768448 146768448 146768448 TGAGCTGGGGAGTGACAGTGGAGATAGTGAGAAGAGGAGGGAATAAAACTGTTAACCATTTCACC TGAGCTGGGGAGTGACAGTGGAGATAGTGAGAGGAGGAGGGAATAAAACTGTTAACCATTTCACC T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:146768445..146768547 26863196 MeRIP-seq:(Medium) rs774457245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9171871 RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514,RMVar_hsa_circ_235328 109938 RMVar_ID_109938 Human_SNP_ID_255317232 m1A Human chr5 + 146873282 146873282 146873282 TCCATCTAATTCTCTCCATCTCTACTGATGCCACCATCCTGGAGCACACCATGACCTCCTAATTA TCCATCTAATTCTCTCCATCTCTACTGATGCCTCCATCCTGGAGCACACCATGACCTCCTAATTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:146873280..146873356 26863196 MeRIP-seq:(Medium) rs1561977319 Functional Loss SNV dbSNP153 33..33 33 - - - 109939 RMVar_ID_109939 Human_SNP_ID_255688062 m1A Human chr5 + 148392636 148392636 148392636 TGTGTGTGTGTGTGTGTATTTGTAATAGCTAAATCCTTGGGAATGAGTACAATTGCCCAGGGAGA TGTGTGTGTGTGTGTGTATTTGTAATAGCTAAGTCCTTGGGAATGAGTACAATTGCCCAGGGAGA A G FBXO38 Ensembl:ENSG00000145868 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:148392633..148392698 26863196 MeRIP-seq:(Medium) rs192171106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24090162 109940 RMVar_ID_109940 Human_SNP_ID_255688662 m1A Human chr5 + 148394817 148394817 148394817 ACGAAAGAAAAGTGTGAAAACATGTATCATGAATAATGAAATTCCAGAAGAAATGACAGCAGATG ACGAAAGAAAAGTGTGAAAACATGTATCATGAGTAATGAAATTCCAGAAGAAATGACAGCAGATG A G FBXO38 Ensembl:ENSG00000145868 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:148394736..148394829 26863196 MeRIP-seq:(Medium) rs761962652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1990138,Human_RBP_ID_26352756 Human_Splice_Rec_707189,Human_Splice_Rec_707229,Human_Splice_Rec_707237,Human_Splice_Rec_707279,Human_Splice_Rec_707287,Human_Splice_Rec_707329,Human_Splice_Rec_707333,Human_Splice_Rec_707339,Human_Splice_Rec_707345,Human_Splice_Rec_707357 RMVar_hsa_circ_51230,RMVar_hsa_circ_316428,RMVar_hsa_circ_365308,RMVar_hsa_circ_369172,RMVar_hsa_circ_350161,RMVar_hsa_circ_359134,RMVar_hsa_circ_332097,RMVar_hsa_circ_272140,RMVar_hsa_circ_304318,RMVar_hsa_circ_315217,RMVar_hsa_circ_278594,RMVar_hsa_circ_58850,RMVar_hsa_circ_62144,RMVar_hsa_circ_53769,RMVar_hsa_circ_235371,RMVar_hsa_circ_235372,RMVar_hsa_circ_235373 109941 RMVar_ID_109941 Human_SNP_ID_255840444 m1A Human chr5 - 149018852 149018852 149018852 TATCAAGGTGGTAGCATTTGAGGAGGCCCTTGAAGGATAAGTAATATCTTGAAAAGTGGAGAAGG TATCAAGGTGGTAGCATTTGAGGAGGCCCTTGGAGGATAAGTAATATCTTGAAAAGTGGAGAAGG T C SH3TC2 Ensembl:ENSG00000169247 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149018804..149018872 26863196 MeRIP-seq:(Medium) rs1028366333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269807 109942 RMVar_ID_109942 Human_SNP_ID_255900167 m1A Human chr5 - 149271946 149271924 149271946 CTCGGTCCATGGCGCCGGCCCGGTCCCCGGGGAGCGGGCCGCAGGGCGCAGGGGCTCCGGCGCGG CTCGGTCCATGGCGCCGGCCCGGTCCCCGGGG______________________CTCCGGCGCGG GCCCCTGCGCCCTGCGGCCCGCT G AC012613.2,AC012613.1 Ensembl:ENSG00000253406,Ensembl:ENSG00000248647 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149271903..149271982 26863196 MeRIP-seq:(Medium) rs1177412077 Functional Loss DEL dbSNP153 33..54 33 - - - 109943 RMVar_ID_109943 Human_SNP_ID_255913681 m1A Human chr5 - 149329722 149329722 149329722 TTTCTCTTTCTCCAGCTTCTCTTTTTCTACCAAGTACCTCCGGGCATCCTCCTCGGCTCGGTTCT TTTCTCTTTCTCCAGCTTCTCTTTTTCTACCAGGTACCTCCGGGCATCCTCCTCGGCTCGGTTCT T C AC131025.3 Ensembl:ENSG00000285736 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149329629..149329823 26863196 MeRIP-seq:(Medium) rs942872338 Functional Loss SNV dbSNP153 33..33 33 - - - 109944 RMVar_ID_109944 Human_SNP_ID_255913690 m1A Human chr5 + 149329753 149329749 149329753 CTTGGTAGAAAAAGAGAAGCTGGAGAAAGAGAAAGAGACGATTCGGACAGAGCTGATAGCACTGA CTTGGTAGAAAAAGAGAAGCTGGAGAAAG____AGAGACGATTCGGACAGAGCTGATAGCACTGA GAGAA G AFAP1L1 Ensembl:ENSG00000157510 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149329703..149329808 26863196 MeRIP-seq:(Medium) rs1211334560 Functional Loss DEL dbSNP153 30..33 33 - - - Human_Splice_Rec_708198,Human_Splice_Rec_708199,Human_Splice_Rec_708264,Human_Splice_Rec_708265,Human_Splice_Rec_708282,Human_Splice_Rec_708283 RMVar_hsa_circ_10338 109945 RMVar_ID_109945 Human_SNP_ID_255917245 m1A Human chr5 - 149345552 149345552 149345552 GCGCTGCACCCGCAGCCGGCCCGCCCACAGCGACCGTACGGCCATGTTTCCAATTTGGGCTGAGA GCGCTGCACCCGCAGCCGGCCCGCCCACAGCGTCCGTACGGCCATGTTTCCAATTTGGGCTGAGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:149345501..149345723 26863196 MeRIP-seq:(Medium) rs763304404 Functional Loss SNV dbSNP153 33..33 33 - - - 109946 RMVar_ID_109946 Human_SNP_ID_255917246 m1A Human chr5 - 149345552 149345552 149345552 GCGCTGCACCCGCAGCCGGCCCGCCCACAGCGACCGTACGGCCATGTTTCCAATTTGGGCTGAGA GCGCTGCACCCGCAGCCGGCCCGCCCACAGCGGCCGTACGGCCATGTTTCCAATTTGGGCTGAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:149345501..149345723 26863196 MeRIP-seq:(Medium) rs763304404 Functional Loss SNV dbSNP153 33..33 33 - - - 109947 RMVar_ID_109947 Human_SNP_ID_255917261 m1A Human chr5 - 149345577 149345577 149345577 CCCACGCGGCACTCCAGGCCAGTAGGCGCTGCACCCGCAGCCGGCCCGCCCACAGCGACCGTACG CCCACGCGGCACTCCAGGCCAGTAGGCGCTGCGCCCGCAGCCGGCCCGCCCACAGCGACCGTACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:149345526..149345730;chr5:149345526..149345800;chr5:149345501..149348400 26863196 MeRIP-seq:(Medium) rs1311707536 Functional Loss SNV dbSNP153 33..33 33 - - - 109948 RMVar_ID_109948 Human_SNP_ID_255920372 m1A Human chr5 - 149358214 149358214 149358214 CGCCCTCCTATACCCCACCTAGCTGAGAACTGAGAACCCTTTACCCGCCGGCCCTCCCCAGCTGG CGCCCTCCTATACCCCACCTAGCTGAGAACTGCGAACCCTTTACCCGCCGGCCCTCCCCAGCTGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:149358164..149358320 26863196 MeRIP-seq:(Medium) rs1354513073 Functional Loss SNV dbSNP153 33..33 33 - - - 109949 RMVar_ID_109949 Human_SNP_ID_255922946 m1A Human chr5 - 149368176 149368176 149368176 CGAAGTAGGACGAGTTGAGGTAGCCGTGGACCAAGGAGACGACGGTGGGCTGGAAAGAGCCCTGC CGAAGTAGGACGAGTTGAGGTAGCCGTGGACCTAGGAGACGACGGTGGGCTGGAAAGAGCCCTGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:149368129..149368397 26863196 MeRIP-seq:(Medium) rs1281699961 Functional Loss SNV dbSNP153 33..33 33 - - - 109950 RMVar_ID_109950 Human_SNP_ID_255922966 m1A Human chr5 - 149368230 149368230 149368230 GGAAATCTGTGGTAAGGATGTTGGCAAAGGGGAAAAGCTTAGGGTCTGGGAAACCGAAGTAGGAC GGAAATCTGTGGTAAGGATGTTGGCAAAGGGGTAAAGCTTAGGGTCTGGGAAACCGAAGTAGGAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149368183..149368255 26863196 MeRIP-seq:(Medium) rs1168644736 Functional Loss SNV dbSNP153 33..33 33 - - - 109951 RMVar_ID_109951 Human_SNP_ID_255922997 m1A Human chr5 - 149368307 149368307 149368307 CTCCTGGGGCTGCTTTCGCCGGAAGCTGGCAGAGATGTTGACAGGGCAGATGTTGTCCAGAGTGC CTCCTGGGGCTGCTTTCGCCGGAAGCTGGCAGGGATGTTGACAGGGCAGATGTTGTCCAGAGTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149368262..149368387 26863196 MeRIP-seq:(Medium) rs377305794 Functional Loss SNV dbSNP153 33..33 33 - - - 109952 RMVar_ID_109952 Human_SNP_ID_255922998 m1A Human chr5 - 149368307 149368307 149368307 CTCCTGGGGCTGCTTTCGCCGGAAGCTGGCAGAGATGTTGACAGGGCAGATGTTGTCCAGAGTGC CTCCTGGGGCTGCTTTCGCCGGAAGCTGGCAGCGATGTTGACAGGGCAGATGTTGTCCAGAGTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149368262..149368387 26863196 MeRIP-seq:(Medium) rs377305794 Functional Loss SNV dbSNP153 33..33 33 - - - 109953 RMVar_ID_109953 Human_SNP_ID_255955435 m1A Human chr5 - 149497732 149497732 149497732 AGTGGGCTAGAATGAGCTATAGTTTCTAGCTCATTTGTAAGGAGGTAGACAAAGGAGCATTGGTG AGTGGGCTAGAATGAGCTATAGTTTCTAGCTCTTTTGTAAGGAGGTAGACAAAGGAGCATTGGTG T A CSNK1A1,AC021078.1 Ensembl:ENSG00000113712,Ensembl:ENSG00000230551 Protein coding,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:149497685..149497871 26863196 MeRIP-seq:(Medium) rs995976961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1109562,Human_RBP_ID_5612598,Human_RBP_ID_7404292,Human_RBP_ID_15347511 109954 RMVar_ID_109954 Human_SNP_ID_255955436 m1A Human chr5 - 149497732 149497732 149497732 AGTGGGCTAGAATGAGCTATAGTTTCTAGCTCATTTGTAAGGAGGTAGACAAAGGAGCATTGGTG AGTGGGCTAGAATGAGCTATAGTTTCTAGCTCGTTTGTAAGGAGGTAGACAAAGGAGCATTGGTG T C CSNK1A1,AC021078.1 Ensembl:ENSG00000113712,Ensembl:ENSG00000230551 Protein coding,lincRNA intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:149497685..149497871 26863196 MeRIP-seq:(Medium) rs995976961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1109562,Human_RBP_ID_5612598,Human_RBP_ID_7404292,Human_RBP_ID_15347511 109955 RMVar_ID_109955 Human_SNP_ID_255968512 m1A Human chr5 + 149550827 149550827 149550827 ATGAGTAAAAGCGCAGCGTTATCGTGAACCCCACCCCAGATGATTACCTCGCCGTTGGTGATGTT ATGAGTAAAAGCGCAGCGTTATCGTGAACCCCCCCCCAGATGATTACCTCGCCGTTGGTGATGTT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:149550826..149551125 32194978 MeRIP-seq:(Medium) rs966803523 Functional Loss SNV dbSNP153 33..33 33 - - - 109956 RMVar_ID_109956 Human_SNP_ID_255968644 m1A Human chr5 - 149551241 149551235 149551242 GCCCCTTTTCCAGCCCGCGACGTCGCCGCGCAAGCGAGGCAGCGGCGGCCGCCGAGAAACAAGTG GCCCCTTTTCCAGCCCGCGACGTCGCCGCGC_______GCAGCGGCGGCCGCCGAGAAACAAGTG CCTCGCTT C CSNK1A1 Ensembl:ENSG00000113712 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:149551190..149551375 26863196 MeRIP-seq:(Medium) rs761989808 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_4845408,Human_RBP_ID_18195253,Human_RBP_ID_18836171,Human_RBP_ID_22099764,Human_RBP_ID_22458997,Human_RBP_ID_22827585,Human_RBP_ID_26827527 RMVar_hsa_circ_265447 109957 RMVar_ID_109957 Human_SNP_ID_255968681 m1A Human chr5 + 149551351 149551351 149551351 TCCGGCCCAGAGGGACCCCTGTCACTCCGCGGACGACGCCATCTTGTTACTCCAGCTCCAGCCAA TCCGGCCCAGAGGGACCCCTGTCACTCCGCGGGCGACGCCATCTTGTTACTCCAGCTCCAGCCAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149551072..149551425 26863196 MeRIP-seq:(Medium) rs542800141 Functional Loss SNV dbSNP153 33..33 33 - - - 109958 RMVar_ID_109958 Human_SNP_ID_256014814 m1A Human chr5 + 149731968 149731968 149731968 GTGGCGGGCGCGCTCGGGTGGGTTCGCGGCAGAGGCCGGAGGGGCTAGTGGCGTGTGATTGCGCT GTGGCGGGCGCGCTCGGGTGGGTTCGCGGCAGGGGCCGGAGGGGCTAGTGGCGTGTGATTGCGCT A G PPARGC1B Ensembl:ENSG00000155846 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149731716..149732045 26863196 MeRIP-seq:(Medium) rs1002314782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267123,Human_RBP_ID_3782912,Human_RBP_ID_5213992,Human_RBP_ID_8136674,Human_RBP_ID_9335402,Human_RBP_ID_17159145,Human_RBP_ID_17415624,Human_RBP_ID_18501852,Human_RBP_ID_21990339,Human_RBP_ID_24385549,Human_RBP_ID_26771560 109959 RMVar_ID_109959 Human_SNP_ID_256014817 m1A Human chr5 + 149731975 149731975 149731975 GCGCGCTCGGGTGGGTTCGCGGCAGAGGCCGGAGGGGCTAGTGGCGTGTGATTGCGCTTCTCGAG GCGCGCTCGGGTGGGTTCGCGGCAGAGGCCGGCGGGGCTAGTGGCGTGTGATTGCGCTTCTCGAG A C PPARGC1B Ensembl:ENSG00000155846 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:149731858..149731990 26863196 MeRIP-seq:(Medium) rs1177634225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_267123,Human_RBP_ID_3782912,Human_RBP_ID_5213992,Human_RBP_ID_8136674,Human_RBP_ID_17159145,Human_RBP_ID_17415624,Human_RBP_ID_18501852,Human_RBP_ID_21990339,Human_RBP_ID_24385549,Human_RBP_ID_26771560 109960 RMVar_ID_109960 Human_SNP_ID_256018924 m1A Human chr5 - 149749369 149749369 149749369 TCTCACATTCCCGTCCAGTTCCTACAACAGTGACCTCAGCGGGTAAGTCACTTCACATCCCTGGG TCTCACATTCCCGTCCAGTTCCTACAACAGTGTCCTCAGCGGGTAAGTCACTTCACATCCCTGGG T A L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149749361..149749483 26863196 MeRIP-seq:(Medium) rs1561851035 Functional Loss SNV dbSNP153 33..33 33 - - - 109961 RMVar_ID_109961 Human_SNP_ID_256030325 m1A Human chr5 + 149796597 149796597 149796597 GAGCAAGTGTGGGAGTGGGAGGCCAGCTGGGCATCTGCTGGAAGTCTAGTAAGAGATGATTGTAT GAGCAAGTGTGGGAGTGGGAGGCCAGCTGGGCTTCTGCTGGAAGTCTAGTAAGAGATGATTGTAT A T PPARGC1B Ensembl:ENSG00000155846 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149796560..149796726 26863196 MeRIP-seq:(Medium) rs1032397685 Functional Loss SNV dbSNP153 33..33 33 - - - 109962 RMVar_ID_109962 Human_SNP_ID_256039482 m1A Human chr5 - 149833267 149833267 149833267 AGGCTTGGTCTGGGCCCGGTGCTCTTGGGTGAAGCTGCGATCCTTACCTCCTCCACCGAGGACGG AGGCTTGGTCTGGGCCCGGTGCTCTTGGGTGAGGCTGCGATCCTTACCTCCTCCACCGAGGACGG T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:149833218..149833459 26863196 MeRIP-seq:(Medium) rs759991233 Functional Loss SNV dbSNP153 33..33 33 - - - 109963 RMVar_ID_109963 Human_SNP_ID_256039529 m1A Human chr5 + 149833371 149833363 149833372 GCCTGCCAGACTGCAGCAGCAGGAGGAGGAAGACGAGGAAGAAGAGGAGGAGGAAGAGGAAGAAG GCCTGCCAGACTGCAGCAGCAGGAG_________GAGGAAGAAGAGGAGGAGGAAGAGGAAGAAG GGAGGAAGAC G PPARGC1B Ensembl:ENSG00000155846 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149833238..149833557 26863196 MeRIP-seq:(Medium) rs757491083 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_4816925,Human_RBP_ID_25872431 RMVar_hsa_circ_3890,RMVar_hsa_circ_116692,RMVar_hsa_circ_235409,RMVar_hsa_circ_358692 109964 RMVar_ID_109964 Human_SNP_ID_256039547 m1A Human chr5 + 149833410 149833408 149833411 AGAAGAGGAGGAGGAAGAGGAAGAAGAAAAAGAGGAGGAGGAGGAGTGGGGCAGGAAAAGGCCAG AGAAGAGGAGGAGGAAGAGGAAGAAGAAAAA___GAGGAGGAGGAGTGGGGCAGGAAAAGGCCAG AGAG A PPARGC1B Ensembl:ENSG00000155846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149833260..149833540 26863196 MeRIP-seq:(Medium) rs775851646 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_76147 RMVar_hsa_circ_3890,RMVar_hsa_circ_116692,RMVar_hsa_circ_235409,RMVar_hsa_circ_358692 109965 RMVar_ID_109965 Human_SNP_ID_256039550 m1A Human chr5 + 149833410 149833410 149833410 AGAAGAGGAGGAGGAAGAGGAAGAAGAAAAAGAGGAGGAGGAGGAGTGGGGCAGGAAAAGGCCAG AGAAGAGGAGGAGGAAGAGGAAGAAGAAAAAGTGGAGGAGGAGGAGTGGGGCAGGAAAAGGCCAG A T PPARGC1B Ensembl:ENSG00000155846 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:149833260..149833540 26863196 MeRIP-seq:(Medium) rs139404347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_76147 RMVar_hsa_circ_3890,RMVar_hsa_circ_116692,RMVar_hsa_circ_235409,RMVar_hsa_circ_358692 109966 RMVar_ID_109966 Human_SNP_ID_256077698 m1A Human chr5 - 149985202 149985202 149985202 TGCTCCAGAGTAGGTCAGCCCAGGCTACCATGAGCTCCTCAGCCCTTTCAGCTTTGGTGAATCTG TGCTCCAGAGTAGGTCAGCCCAGGCTACCATGCGCTCCTCAGCCCTTTCAGCTTTGGTGAATCTG T G L13705-009,L13304-001,lnc-TIGD6-1 RNACentral:URS00001E2917,RNACentral:URS000044B5AA,RNACentral:URS00008BB414 misc_RNA,scRNA,lincRNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:149985156..149985284 32194978 MeRIP-seq:(Medium) rs547241031 Functional Loss SNV dbSNP153 33..33 33 - - - 109967 RMVar_ID_109967 Human_SNP_ID_376553150 m1A Human chr8 + 106270367 106270367 106270367 CGCTCACCGCAGCCCCCTCCTGGCGACCCGCAAGTAAGTTTGTGAGGCTGCTGGGCGTTAGGGCG CGCTCACCGCAGCCCCCTCCTGGCGACCCGCAGGTAAGTTTGTGAGGCTGCTGGGCGTTAGGGCG A G AC027031.2 Ensembl:ENSG00000254615 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:106270283..106270446 26863410 MeRIP-seq:(Medium) rs997435360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1000355,Human_Splice_Rec_1000357,Human_Splice_Rec_1000359,Human_Splice_Rec_1000361 109968 RMVar_ID_109968 Human_SNP_ID_376553234 m1A Human chr8 - 106270679 106270679 106270679 TGTCCCTGGCCGGGCTCCCGCGCCCCAAACCCAGCCTCCCCGCCCGGTCTCCTCCCTCGCCGCCC TGTCCCTGGCCGGGCTCCCGCGCCCCAAACCCGGCCTCCCCGCCCGGTCTCCTCCCTCGCCGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:106270254..106271725 26863196 MeRIP-seq:(Medium) rs1403052904 Functional Loss SNV dbSNP153 33..33 33 - - - 109969 RMVar_ID_109969 Human_SNP_ID_376660592 m1A Human chr8 + 106725253 106725253 106725253 TGTGAGTGCATGCTGGAATGTGGAGGAAGGAGATGGGAGTGGGGGTTTGGTTGGGATGCAGTATT TGTGAGTGCATGCTGGAATGTGGAGGAAGGAGTTGGGAGTGGGGGTTTGGTTGGGATGCAGTATT A T OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:106725203..106725312 26863196 MeRIP-seq:(Medium) rs963923497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8221173,Human_RBP_ID_17210242,Human_RBP_ID_18961032,Human_RBP_ID_21995302 RMVar_hsa_circ_97391,RMVar_hsa_circ_253837,RMVar_hsa_circ_269334,RMVar_hsa_circ_60258,RMVar_hsa_circ_372557,RMVar_hsa_circ_253842,RMVar_hsa_circ_66309 109970 RMVar_ID_109970 Human_SNP_ID_376809055 m1A Human chr8 - 107336261 107336261 107336261 TATTTTCATCTTTTATCTTAAGGTACTAAATCAAACTTCTCGACTTGAGATACAGCTGCTGGAGA TATTTTCATCTTTTATCTTAAGGTACTAAATCTAACTTCTCGACTTGAGATACAGCTGCTGGAGA T A ANGPT1 Ensembl:ENSG00000154188 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:107336222..107336299 26863196 MeRIP-seq:(Medium) rs772112333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957831 Human_Splice_Rec_1000596,Human_Splice_Rec_1000612,Human_Splice_Rec_1000626,Human_Splice_Rec_1000640 RMVar_hsa_circ_9672,RMVar_hsa_circ_82568,RMVar_hsa_circ_341247,RMVar_hsa_circ_362464,RMVar_hsa_circ_253848,RMVar_hsa_circ_253847,RMVar_hsa_circ_38575,RMVar_hsa_circ_64409,RMVar_hsa_circ_253849,RMVar_hsa_circ_316994 109971 RMVar_ID_109971 Human_SNP_ID_377042959 m1A Human chr8 - 108248570 108248570 108248570 CTTTGGGCGCAAGGAAGGCGTGGGGGCGGATGAGGTGCTGAGCAAGGCCGAAAGGTGGTGTCTGT CTTTGGGCGCAAGGAAGGCGTGGGGGCGGATGCGGTGCTGAGCAAGGCCGAAAGGTGGTGTCTGT T G EIF3E Ensembl:ENSG00000104408 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:108248480..108248627 26863196 MeRIP-seq:(Medium) rs776055807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255275,Human_RBP_ID_796679,Human_RBP_ID_844627,Human_RBP_ID_7799566,Human_RBP_ID_16317142,Human_RBP_ID_17172888,Human_RBP_ID_21995563,Human_RBP_ID_24240481 109972 RMVar_ID_109972 Human_SNP_ID_377088669 m1A Human chr8 + 108449802 108449802 108449802 GTATGTGTGTGTCTGGGTACATATACACTTAAATGTCATGTTATTTTTTTCAGAAATGAGAGATA GTATGTGTGTGTCTGGGTACATATACACTTAAGTGTCATGTTATTTTTTTCAGAAATGAGAGATA A G EMC2 Ensembl:ENSG00000104412 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:108449799..108449950 26863196 MeRIP-seq:(Medium) rs1305634753 Functional Loss SNV dbSNP153 33..33 33 - - - 109973 RMVar_ID_109973 Human_SNP_ID_377300939 m1A Human chr8 + 109334410 109334410 109334410 TAAGTCCGGGCAGCCGAAGAGTGTGGTAGGTAACGGTCCTCAGCGCAAGGGTCATTTCGTCGCTG TAAGTCCGGGCAGCCGAAGAGTGTGGTAGGTAGCGGTCCTCAGCGCAAGGGTCATTTCGTCGCTG A G ENY2 Ensembl:ENSG00000120533 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:109334326..109334537 26863196 MeRIP-seq:(Medium) rs1332085505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255320,Human_RBP_ID_693125,Human_RBP_ID_796265,Human_RBP_ID_4968107,Human_RBP_ID_5328903,Human_RBP_ID_18426738,Human_RBP_ID_24241108,Human_RBP_ID_27843312 Human_Splice_Rec_1001145,Human_Splice_Rec_1001175,Human_Splice_Rec_1001181,Human_Splice_Rec_1001189,Human_Splice_Rec_1001191,Human_Splice_Rec_1001199,Human_Splice_Rec_1001203 109974 RMVar_ID_109974 Human_SNP_ID_377352682 m1A Human chr8 - 109539798 109539798 109539798 GTCTCTTCCTCGAGCTCGCGCTCCGCCCGCTCACTCCCAGCCCCGCTCATTCAAAGCCGGGCGCG GTCTCTTCCTCGAGCTCGCGCTCCGCCCGCTCCCTCCCAGCCCCGCTCATTCAAAGCCGGGCGCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:109539721..109539913;chr8:109539748..109539892 26863196 MeRIP-seq:(Medium) rs1296191346 Functional Loss SNV dbSNP153 33..33 33 - - - 109975 RMVar_ID_109975 Human_SNP_ID_378808638 m1A Human chr8 - 115420233 115420233 115420233 TGCAGTAGGCCTTCACTGGGACTTGCAGACTGACACCCAACATTTGCTATTGCAATGTTATTGAG TGCAGTAGGCCTTCACTGGGACTTGCAGACTGGCACCCAACATTTGCTATTGCAATGTTATTGAG T C TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:115420097..115420357 26863196 MeRIP-seq:(Medium) rs1247383561 Functional Loss SNV dbSNP153 33..33 33 - - - 109976 RMVar_ID_109976 Human_SNP_ID_378834553 m1A Human chr8 - 115531971 115531971 115531971 CAGTCCCTCAGATTTCGTCATTCCTCATGGCAACAGCCCCATACAACCAGCAACTCAGAAACCCC CAGTCCCTCAGATTTCGTCATTCCTCATGGCAGCAGCCCCATACAACCAGCAACTCAGAAACCCC T C TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:115531896..115532009 26863196 MeRIP-seq:(Medium) rs773638260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21575028 109977 RMVar_ID_109977 Human_SNP_ID_379096915 m1A Human chr8 - 116644963 116644963 116644963 TTTCCAGAAAAGAAGTTAACATGAACTCTTGAAGTCACACCAGGGCAACTCTTGGAAGAAATATA TTTCCAGAAAAGAAGTTAACATGAACTCTTGAGGTCACACCAGGGCAACTCTTGGAAGAAATATA T C EIF3H Ensembl:ENSG00000147677 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1042450031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89851,Human_RBP_ID_693424,Human_RBP_ID_1054134,Human_RBP_ID_1692624,Human_RBP_ID_2051854,Human_RBP_ID_3871536,Human_RBP_ID_8678228,Human_RBP_ID_9220095,Human_RBP_ID_16324652,Human_RBP_ID_17316952,Human_RBP_ID_17431732,Human_RBP_ID_17544263,Human_RBP_ID_18890567,Human_RBP_ID_21953385,Human_RBP_ID_23216184,Human_RBP_ID_26832361,Human_RBP_ID_27535471,Human_RBP_ID_27773430 Human_miRNA_ID_252444,Human_miRNA_ID_861754,Human_miRNA_ID_1465060 109978 RMVar_ID_109978 Human_SNP_ID_379097305 m1A Human chr8 - 116646536 116646536 116646536 CCAGAGCCGAGGAGAACCCCCGCTCCCTGAGGAGGACCTGTCCAAACTCTTCAAACCACCACAGC CCAGAGCCGAGGAGAACCCCCGCTCCCTGAGGGGGACCTGTCCAAACTCTTCAAACCACCACAGC T C EIF3H Ensembl:ENSG00000147677 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:116646451..116646575 26863196 MeRIP-seq:(Medium) rs1432787275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693435,Human_RBP_ID_796349,Human_RBP_ID_5430026,Human_RBP_ID_5452994,Human_RBP_ID_5480539,Human_RBP_ID_5514178,Human_RBP_ID_9220098,Human_RBP_ID_18196522,Human_RBP_ID_26832365 Human_Splice_Rec_1002972,Human_Splice_Rec_1002973,Human_Splice_Rec_1002986,Human_Splice_Rec_1002987,Human_Splice_Rec_1003004,Human_Splice_Rec_1003005,Human_Splice_Rec_1003012 RMVar_hsa_circ_2750,RMVar_hsa_circ_299166,RMVar_hsa_circ_55681,RMVar_hsa_circ_253978 109979 RMVar_ID_109979 Human_SNP_ID_379097321 m1A Human chr8 - 116646564 116646564 116646564 AGCGTCGCCAGCAGGAGAATATGCAGCGCCAGAGCCGAGGAGAACCCCCGCTCCCTGAGGAGGAC AGCGTCGCCAGCAGGAGAATATGCAGCGCCAGGGCCGAGGAGAACCCCCGCTCCCTGAGGAGGAC T C EIF3H Ensembl:ENSG00000147677 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:116646501..116646625 26863196 MeRIP-seq:(Medium) rs768608670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796349,Human_RBP_ID_5430032,Human_RBP_ID_5514182,Human_RBP_ID_26832367 Human_Splice_Rec_1002972,Human_Splice_Rec_1002973,Human_Splice_Rec_1002986,Human_Splice_Rec_1002987,Human_Splice_Rec_1003004,Human_Splice_Rec_1003005,Human_Splice_Rec_1003012 RMVar_hsa_circ_2750,RMVar_hsa_circ_299166,RMVar_hsa_circ_55681,RMVar_hsa_circ_253978 109980 RMVar_ID_109980 Human_SNP_ID_379124858 m1A Human chr8 + 116755758 116755758 116755758 TTTCCCTGCTGCGCCGGCGGTGGAGCTGGAAGAGGTGGCAGTAGAGCCGGTACCTTCCTTGCGGG TTTCCCTGCTGCGCCGGCGGTGGAGCTGGAAGGGGTGGCAGTAGAGCCGGTACCTTCCTTGCGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr8:116755668..116755825;chr8:116755708..116755825 26863196 MeRIP-seq:(Medium) rs778048842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5430091,Human_RBP_ID_5480611,Human_RBP_ID_5514257 109981 RMVar_ID_109981 Human_SNP_ID_379124876 m1A Human chr8 - 116755776 116755776 116755776 TGCTTGGAAAGATGGCGTCCCGCAAGGAAGGTACCGGCTCTACTGCCACCTCTTCCAGCTCCACC TGCTTGGAAAGATGGCGTCCCGCAAGGAAGGTGCCGGCTCTACTGCCACCTCTTCCAGCTCCACC T C EIF3H Ensembl:ENSG00000147677 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:116755726..116755825 26863196 MeRIP-seq:(Medium) rs750077223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693460,Human_RBP_ID_960652,Human_RBP_ID_1054147,Human_RBP_ID_1692639,Human_RBP_ID_4968858,Human_RBP_ID_5430094,Human_RBP_ID_5453067,Human_RBP_ID_5480613,Human_RBP_ID_5514260,Human_RBP_ID_22465965 Human_Splice_Rec_1002992,Human_Splice_Rec_1003062 RMVar_hsa_circ_61905,RMVar_hsa_circ_100103,RMVar_hsa_circ_62011,RMVar_hsa_circ_253980 109982 RMVar_ID_109982 Human_SNP_ID_379146415 m1A Human chr8 + 116846269 116846269 116846269 CATTTCACATAATTTTAAATTATTGGGTATACACTGAAGTCTGAGTTTCAAAAGTGATTTTTTTT CATTTCACATAATTTTAAATTATTGGGTATACGCTGAAGTCTGAGTTTCAAAAGTGATTTTTTTT A G UTP23 Ensembl:ENSG00000147679 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:116846184..116846284 32194978 MeRIP-seq:(Medium) rs1203232333 Functional Loss SNV dbSNP153 33..33 33 - - - 109983 RMVar_ID_109983 Human_SNP_ID_379147151 m1A Human chr8 - 116849007 116849007 116849007 TTTTATTCAGGATGAAGATGCATCAGGGGGCGATCAAGATCAGGAAGAAAGAAGATGGAACAAAA TTTTATTCAGGATGAAGATGCATCAGGGGGCGGTCAAGATCAGGAAGAAAGAAGATGGAACAAAA T C RAD21 Ensembl:ENSG00000164754 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:116848951..116849050 32194978 MeRIP-seq:(Medium) rs1445046720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88849,Human_RBP_ID_218197,Human_RBP_ID_254990,Human_RBP_ID_845501,Human_RBP_ID_959305,Human_RBP_ID_1700113,Human_RBP_ID_3132578,Human_RBP_ID_7804053,Human_RBP_ID_8273883,Human_RBP_ID_8916216,Human_RBP_ID_9405706,Human_RBP_ID_18541389,Human_RBP_ID_23087902,Human_RBP_ID_23117126,Human_RBP_ID_23120722,Human_RBP_ID_24549408,Human_RBP_ID_26189025,Human_RBP_ID_26358740,Human_RBP_ID_27120060,Human_RBP_ID_27831530 Human_Splice_Rec_1003118,Human_Splice_Rec_1003119,Human_Splice_Rec_1003122,Human_Splice_Rec_1003123,Human_Splice_Rec_1003125,Human_Splice_Rec_1003130,Human_Splice_Rec_1003131 RMVar_hsa_circ_81366,RMVar_hsa_circ_127215,RMVar_hsa_circ_117090,RMVar_hsa_circ_118906,RMVar_hsa_circ_102141,RMVar_hsa_circ_253992,RMVar_hsa_circ_253994,RMVar_hsa_circ_253995,RMVar_hsa_circ_253996,RMVar_hsa_circ_253993,RMVar_hsa_circ_266834 109984 RMVar_ID_109984 Human_SNP_ID_379149078 m1A Human chr8 - 116856290 116856290 116856290 TTGTGACTTTTTTTTTTTTTTTTTTTTTTTACAGTGGGTGGGCCTGATAGTCCTGATTCAGTGGA TTGTGACTTTTTTTTTTTTTTTTTTTTTTTACGGTGGGTGGGCCTGATAGTCCTGATTCAGTGGA T C RAD21 Ensembl:ENSG00000164754 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:116856245..116857297 32194978 MeRIP-seq:(Medium) rs1284975068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960896,Human_RBP_ID_4968985,Human_RBP_ID_18125075,Human_RBP_ID_22688462,Human_RBP_ID_24563397,Human_RBP_ID_26146773 RMVar_hsa_circ_81366,RMVar_hsa_circ_117090,RMVar_hsa_circ_118906,RMVar_hsa_circ_4456,RMVar_hsa_circ_253994,RMVar_hsa_circ_253995,RMVar_hsa_circ_253996,RMVar_hsa_circ_53303,RMVar_hsa_circ_269793,RMVar_hsa_circ_266834,RMVar_hsa_circ_65470,RMVar_hsa_circ_126210,RMVar_hsa_circ_45020,RMVar_hsa_circ_253998,RMVar_hsa_circ_316073,RMVar_hsa_circ_46851,RMVar_hsa_circ_283785,RMVar_hsa_circ_333235,RMVar_hsa_circ_25504,RMVar_hsa_circ_306550 109985 RMVar_ID_109985 Human_SNP_ID_379154025 m1A Human chr8 + 116874132 116874132 116874132 ACTTTCTTGAGCCCCGCACCCGAGTTCGGCGGAAGGTTGCTGCTCCCGGGGCTGGCACCGCGGGC ACTTTCTTGAGCCCCGCACCCGAGTTCGGCGGCAGGTTGCTGCTCCCGGGGCTGGCACCGCGGGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:116874125..116874613 26863196 MeRIP-seq:(Medium) rs956952460 Functional Loss SNV dbSNP153 33..33 33 - - - 109986 RMVar_ID_109986 Human_SNP_ID_379154254 m1A Human chr8 - 116874623 116874623 116874623 CCTCCCCGGGCCACCCAGCCCGCCCAACTCCCAGCGGAGAGCAAGGTAAGAGACTCGGCCGACCC CCTCCCCGGGCCACCCAGCCCGCCCAACTCCCGGCGGAGAGCAAGGTAAGAGACTCGGCCGACCC T C RAD21 Ensembl:ENSG00000164754 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:116874601..116874675 26863196 MeRIP-seq:(Medium) rs1461435275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_693537,Human_RBP_ID_795882,Human_RBP_ID_4996292,Human_RBP_ID_5480619,Human_RBP_ID_17093938,Human_RBP_ID_18961035 Human_Splice_Rec_1003095 RMVar_hsa_circ_81366,RMVar_hsa_circ_253996,RMVar_hsa_circ_126210,RMVar_hsa_circ_253998 109987 RMVar_ID_109987 Human_SNP_ID_379154267 m1A Human chr8 + 116874661 116874661 116874661 TTGGGCGGGCTGGGTGGCCCGGGGAGGGGAAAAGGGTCGGGGGAGGGGGTGGGGAAAGGGGGGAG TTGGGCGGGCTGGGTGGCCCGGGGAGGGGAAAGGGGTCGGGGGAGGGGGTGGGGAAAGGGGGGAG A G RAD21-AS1 Ensembl:ENSG00000253327 lincRNA exon GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Hypoxia IP chr8:116874498..116874775;chr8:116874570..116874816 26863196,32194978 MeRIP-seq:(Medium) rs1195719401 Functional Loss SNV dbSNP153 33..33 33 - - - 109988 RMVar_ID_109988 Human_SNP_ID_379154301 m1A Human chr8 - 116874722 116874722 116874722 GGAAAGGAGGCGCCGGCTGTGGCGGCGGCGGGAGCTGCTCGGAAGCTACACCTCGCAAGGGCTCC GGAAAGGAGGCGCCGGCTGTGGCGGCGGCGGGGGCTGCTCGGAAGCTACACCTCGCAAGGGCTCC T C RAD21 Ensembl:ENSG00000164754 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:116874626..116874816 26863410 MeRIP-seq:(Medium) rs1055574966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845507,Human_RBP_ID_4995678,Human_RBP_ID_5154099,Human_RBP_ID_8923593,Human_RBP_ID_16328320,Human_RBP_ID_18427111,Human_RBP_ID_18961626,Human_RBP_ID_22115117,Human_RBP_ID_22465968,Human_RBP_ID_22626880,Human_RBP_ID_24242384 RMVar_hsa_circ_81366,RMVar_hsa_circ_253996,RMVar_hsa_circ_126210,RMVar_hsa_circ_253998 109989 RMVar_ID_109989 Human_SNP_ID_379154312 m1A Human chr8 + 116874737 116874737 116874737 TGTAGCTTCCGAGCAGCTCCCGCCGCCGCCACAGCCGGCGCCTCCTTTCCGATTCACTCAAACAA TGTAGCTTCCGAGCAGCTCCCGCCGCCGCCACTGCCGGCGCCTCCTTTCCGATTCACTCAAACAA A T RAD21-AS1 Ensembl:ENSG00000253327 lincRNA exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:116874701..116874775;chr8:116874651..116874800;chr8:116874695..116874785;chr8:116874693..116874802 26863196 MeRIP-seq:(Medium) rs1563697344 Functional Loss SNV dbSNP153 33..33 33 - - - 109990 RMVar_ID_109990 Human_SNP_ID_379308555 m1A Human chr8 + 117530810 117530810 117530810 CACCTCGTTTTGCTAGTGAAGAGAGGCGAGAAATTGCTGAAGTAAATAAAGTGAGTTGTTAGTTT CACCTCGTTTTGCTAGTGAAGAGAGGCGAGAACTTGCTGAAGTAAATAAAGTGAGTTGTTAGTTT A C MED30 Ensembl:ENSG00000164758 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:117530759..117539964 32194978 MeRIP-seq:(Medium) rs770113741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1003288,Human_Splice_Rec_1003289,Human_Splice_Rec_1003297 RMVar_hsa_circ_254000,RMVar_hsa_circ_273889 109991 RMVar_ID_109991 Human_SNP_ID_379374401 m1A Human chr8 + 117812856 117812856 117812856 TGACTGCCTGAACAGCCCACCTGCTGCTCCTCAGGCATGGGTTCTTACCTCTGTTGTTGAAAGCA TGACTGCCTGAACAGCCCACCTGCTGCTCCTCTGGCATGGGTTCTTACCTCTGTTGTTGAAAGCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:117812851..117812975 32194978 MeRIP-seq:(Medium) rs1171922196 Functional Loss SNV dbSNP153 33..33 33 - - - 109992 RMVar_ID_109992 Human_SNP_ID_379403443 m1A Human chr8 - 117933910 117933910 117933910 GCTCTGTGAAGAGGGCATCTTCACGTGGAGCAAGGCTGGACAGCAGGAGCCCACTAGGGACCCCT GCTCTGTGAAGAGGGCATCTTCACGTGGAGCAGGGCTGGACAGCAGGAGCCCACTAGGGACCCCT T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:117933908..117934027 26863196 MeRIP-seq:(Medium) rs1266263426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 109993 RMVar_ID_109993 Human_SNP_ID_379408615 m1A Human chr8 + 117955575 117955575 117955575 TTGGGTGTCAAGGGGCAGAGACCAAATTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAA TTGGGTGTCAAGGGGCAGAGACCAAATTTTTGCGACAGAGTCTCACTCTGTTGCCCAGGCTGGAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:117955574..117955674 32194978 MeRIP-seq:(Medium) rs1465547747 Functional Loss SNV dbSNP153 33..33 33 - - - 109994 RMVar_ID_109994 Human_SNP_ID_379446400 m1A Human chr8 + 118111404 118111404 118111404 GGGGAGAAAAAAAAAGCTCCCGATACCCAATCAATGGCAAGACGAAGTGATTGCCTTGCCTCTCG GGGGAGAAAAAAAAAGCTCCCGATACCCAATCGATGGCAAGACGAAGTGATTGCCTTGCCTCTCG A G UCG.246 RNACentral:URS000036BE0B misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:118111354..118111753 32194978 MeRIP-seq:(Medium) rs886062639 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_737 109995 RMVar_ID_109995 Human_SNP_ID_379446485 m1A Human chr8 - 118111722 118111700 118111722 ACTGCCCGCGGGGAGGACGCGCCGCCGCCGCCACCCAGCGCCGCCGCCGCCGCCGCCTCCAGCCG ACTGCCCGCGGGGAGGACGCGCCGCCGCCGCC______________________GCCTCCAGCCG CGGCGGCGGCGGCGGCGCTGGGT C EXT1 Ensembl:ENSG00000182197 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:118111642..118111734 26863410 MeRIP-seq:(Medium) rs928631288 Functional Loss DEL dbSNP153 33..54 33 - - - Human_RBP_ID_4995151,Human_RBP_ID_5534307,Human_RBP_ID_18426885,Human_RBP_ID_22465262 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 109996 RMVar_ID_109996 Human_SNP_ID_379446488 m1A Human chr8 - 118111722 118111703 118111722 ACTGCCCGCGGGGAGGACGCGCCGCCGCCGCCACCCAGCGCCGCCGCCGCCGCCGCCTCCAGCCG ACTGCCCGCGGGGAGGACGCGCCGCCGCCGCC___________________GCCGCCTCCAGCCG CGGCGGCGGCGGCGCTGGGT C EXT1 Ensembl:ENSG00000182197 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:118111642..118111734 26863410 MeRIP-seq:(Medium) rs937343061 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_4995151,Human_RBP_ID_5534307,Human_RBP_ID_18426885,Human_RBP_ID_22465262 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 109997 RMVar_ID_109997 Human_SNP_ID_379874153 m1A Human chr8 + 119822926 119822925 119822926 TTTTTCTCCCTTCACCCTAAATCCTTAAATTCAACCACTCCTCTGCCAACTACCAATTACCTTGC TTTTTCTCCCTTCACCCTAAATCCTTAAATTC_ACCACTCCTCTGCCAACTACCAATTACCTTGC CA C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:119822925..119823057 26863196 MeRIP-seq:(Medium) rs1390112658 Functional Loss DEL dbSNP153 33..33 33 - - - 109998 RMVar_ID_109998 Human_SNP_ID_379874157 m1A Human chr8 - 119822944 119822944 119822944 GGTACGTGAAACAGAGGGGCAAGGTAATTGGTAGTTGGCAGAGGAGTGGTTGAATTTAAGGATTT GGTACGTGAAACAGAGGGGCAAGGTAATTGGTGGTTGGCAGAGGAGTGGTTGAATTTAAGGATTT T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:119822916..119823068 26863196 MeRIP-seq:(Medium) rs1404385738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16336092 RMVar_hsa_circ_92193,RMVar_hsa_circ_254056,RMVar_hsa_circ_254075,RMVar_hsa_circ_254077,RMVar_hsa_circ_254081,RMVar_hsa_circ_254085 109999 RMVar_ID_109999 Human_SNP_ID_379882326 m1A Human chr8 + 119855814 119855814 119855814 CGGGTCCTCTTCATCGCAGCGCCGGGTCTAGGAGTCCCGCCGCGCCCGGGTGGCTGCGGGCTTGG CGGGTCCTCTTCATCGCAGCGCCGGGTCTAGGGGTCCCGCCGCGCCCGGGTGGCTGCGGGCTTGG A G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:119855765..119855844 26863196 MeRIP-seq:(Medium) rs1351040196 Functional Loss SNV dbSNP153 33..33 33 - - - 110000 RMVar_ID_110000 Human_SNP_ID_379886569 m1A Human chr8 + 119873812 119873811 119873812 GACTGATCCGAGCACCCAAACCCTCGGCGGACAGCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA GACTGATCCGAGCACCCAAACCCTCGGCGGAC_GCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA CA C DEPTOR Ensembl:ENSG00000155792 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:119873763..119873964 26863196 MeRIP-seq:(Medium) rs1563952946 Functional Loss DEL dbSNP153 33..33 33 - - - 110001 RMVar_ID_110001 Human_SNP_ID_379886570 m1A Human chr8 + 119873812 119873812 119873812 GACTGATCCGAGCACCCAAACCCTCGGCGGACAGCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA GACTGATCCGAGCACCCAAACCCTCGGCGGACGGCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA A G DEPTOR Ensembl:ENSG00000155792 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:119873763..119873964 26863196 MeRIP-seq:(Medium) rs755503280 Functional Loss SNV dbSNP153 33..33 33 - - - 110002 RMVar_ID_110002 Human_SNP_ID_379886571 m1A Human chr8 + 119873812 119873812 119873812 GACTGATCCGAGCACCCAAACCCTCGGCGGACAGCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA GACTGATCCGAGCACCCAAACCCTCGGCGGACTGCGGAGCCAGTGGTAGCCGCACGGCCCTAAAA A T DEPTOR Ensembl:ENSG00000155792 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:119873763..119873964 26863196 MeRIP-seq:(Medium) rs755503280 Functional Loss SNV dbSNP153 33..33 33 - - - 110003 RMVar_ID_110003 Human_SNP_ID_379886596 m1A Human chr8 - 119873840 119873840 119873840 CTGCCAGTGCTGCCGCCCTCCTCCATGGTTTTAGGGCCGTGCGGCTACCACTGGCTCCGCTGTCC CTGCCAGTGCTGCCGCCCTCCTCCATGGTTTTGGGGCCGTGCGGCTACCACTGGCTCCGCTGTCC T C AP005717.1 Ensembl:ENSG00000245330 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:119873800..119873935;chr8:119873796..119873908 26863196 MeRIP-seq:(Medium) rs774358933 Functional Loss SNV dbSNP153 33..33 33 - - - 110004 RMVar_ID_110004 Human_SNP_ID_379900044 m1A Human chr8 + 119928365 119928365 119928365 CTGGGATTGGTTTAATAATTTGTGCTGTCATCAGAATTTCCAAAGTAATTGCTAATTTTTCTTTC CTGGGATTGGTTTAATAATTTGTGCTGTCATCTGAATTTCCAAAGTAATTGCTAATTTTTCTTTC A T DEPTOR Ensembl:ENSG00000155792 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:119928364..119928453 26863196 MeRIP-seq:(Medium) rs1184505440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8678822 110005 RMVar_ID_110005 Human_SNP_ID_357712876 m1A Human chr8 - 30069771 30069771 30069771 TGGTACTCCTTGGGATCGCGTTTGTAGTCTATAAGCTGTTCCTGAGTGACGGGCAGTATTCTCCT TGGTACTCCTTGGGATCGCGTTTGTAGTCTATGAGCTGTTCCTGAGTGACGGGCAGTATTCTCCT T C SARAF Ensembl:ENSG00000133872 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:30069751..30069775 26863196 MeRIP-seq:(Medium) rs1254369333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_698308,Human_RBP_ID_1055399,Human_RBP_ID_5000266,Human_RBP_ID_22776299,Human_RBP_ID_24255176 Human_miRNA_ID_1509521,Human_miRNA_ID_2205165,Human_miRNA_ID_2770413,Human_miRNA_ID_2928899,Human_miRNA_ID_2996264,Human_miRNA_ID_3088034 RMVar_hsa_circ_11575,RMVar_hsa_circ_33886,RMVar_hsa_circ_284023,RMVar_hsa_circ_289170,RMVar_hsa_circ_128053,RMVar_hsa_circ_251070,RMVar_hsa_circ_251071,RMVar_hsa_circ_251069 110006 RMVar_ID_110006 Human_SNP_ID_357716350 m1A Human chr8 + 30082948 30082948 30082948 ACCCGGCCGCTCCCGGCCCGCAGGCTGCGGCCATGGCGCTCGATGAAGATGGCGCCGGGCTGCCA ACCCGGCCGCTCCCGGCCCGCAGGCTGCGGCCTTGGCGCTCGATGAAGATGGCGCCGGGCTGCCA A T AC044849.1 Ensembl:ENSG00000272256 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr8:30082901..30083046;chr8:30082926..30082950 26863196 MeRIP-seq:(Medium) rs974847329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633298 110007 RMVar_ID_110007 Human_SNP_ID_357719947 m1A Human chr8 + 30095507 30095507 30095507 CCGCCTCGGGTCGTGGAGCCAGGAGCGACGTCACCGCCATGGCAGGCATCAAAGGTGGGCCTGGG CCGCCTCGGGTCGTGGAGCCAGGAGCGACGTCGCCGCCATGGCAGGCATCAAAGGTGGGCCTGGG A G LEPROTL1 Ensembl:ENSG00000104660 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:30095457..30095571 26863196 MeRIP-seq:(Medium) rs1308889622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254793,Human_RBP_ID_845140,Human_RBP_ID_960092,Human_RBP_ID_4994978,Human_RBP_ID_5243489,Human_RBP_ID_19141029,Human_RBP_ID_22465183 Human_Splice_Rec_963183,Human_Splice_Rec_963189,Human_Splice_Rec_963193,Human_Splice_Rec_963199,Human_Splice_Rec_963205,Human_Splice_Rec_963213,Human_Splice_Rec_963219 RMVar_hsa_circ_94537,RMVar_hsa_circ_251073 110008 RMVar_ID_110008 Human_SNP_ID_357719955 m1A Human chr8 + 30095526 30095526 30095526 CAGGAGCGACGTCACCGCCATGGCAGGCATCAAAGGTGGGCCTGGGTTGCAGGACGCGGGAGGGC CAGGAGCGACGTCACCGCCATGGCAGGCATCACAGGTGGGCCTGGGTTGCAGGACGCGGGAGGGC A C LEPROTL1 Ensembl:ENSG00000104660 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:30095426..30095557 26863410 MeRIP-seq:(Medium) rs1243687354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995406,Human_RBP_ID_5406479,Human_RBP_ID_19141029 Human_Splice_Rec_963183,Human_Splice_Rec_963189,Human_Splice_Rec_963193,Human_Splice_Rec_963199,Human_Splice_Rec_963205,Human_Splice_Rec_963213,Human_Splice_Rec_963219 RMVar_hsa_circ_94537,RMVar_hsa_circ_251073 110009 RMVar_ID_110009 Human_SNP_ID_357737158 m1A Human chr8 - 30164137 30164137 30164137 TTACATCTCCTCTGATTTCACTTTCTACACATACAACTGCTCCAGGAGCAATCTTCACACTGTAG TTACATCTCCTCTGATTTCACTTTCTACACATGCAACTGCTCCAGGAGCAATCTTCACACTGTAG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:30164087..30164217 26863410 MeRIP-seq:(Medium) rs750675730 Functional Loss SNV dbSNP153 33..33 33 - - - 110010 RMVar_ID_110010 Human_SNP_ID_357782502 m1A Human chr8 + 30352477 30352474 30352477 AATGGGCACTCTCCTTATCAGCAAGATCCGAGAAGAATACCCTGATCGCATCATGAATACCTTCA AATGGGCACTCTCCTTATCAGCAAGATCCG___AGAATACCCTGATCGCATCATGAATACCTTCA GAGA G TUBBP1 Ensembl:ENSG00000127589 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1473100494 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17434551 110011 RMVar_ID_110011 Human_SNP_ID_357782643 m1A Human chr8 + 30352954 30352954 30352954 CCGCCACGGCCGATACCTCACCGTGGCTGCTGACTTCCGTGGTCGGATGTCCATGAAGGAGGTCG CCGCCACGGCCGATACCTCACCGTGGCTGCTGTCTTCCGTGGTCGGATGTCCATGAAGGAGGTCG A T TUBBP1 Ensembl:ENSG00000127589 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs887058274 Functional Loss SNV dbSNP153 33..33 33 - - - 110012 RMVar_ID_110012 Human_SNP_ID_357790519 m1A Human chr8 + 30384934 30384934 30384934 CAGACTCGCCGCGGGAGCCCCAGCCCAACCCGAGCCCGACAGCCACTGCCCCGGCTCCAGCTCCA CAGACTCGCCGCGGGAGCCCCAGCCCAACCCGGGCCCGACAGCCACTGCCCCGGCTCCAGCTCCA A G RBPMS Ensembl:ENSG00000157110 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:30384510..30385258;chr8:30384467..30385128 26863196 MeRIP-seq:(Medium) rs1208459274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5134999,Human_RBP_ID_24563425 Human_miRNA_ID_1014197,Human_miRNA_ID_1200953,Human_miRNA_ID_1296206,Human_miRNA_ID_1300141,Human_miRNA_ID_2457096,Human_miRNA_ID_2462017,Human_miRNA_ID_2579664,Human_miRNA_ID_2634663,Human_miRNA_ID_2637350 RMVar_hsa_circ_108878,RMVar_hsa_circ_251096 110013 RMVar_ID_110013 Human_SNP_ID_357857256 m1A Human chr8 - 30653601 30653601 30653601 TGTATTAAAGACACTTATTTTTTCTTTGTAGCATTATGGATCCAAGCCTGTTGAGAGAAAGGGAG TGTATTAAAGACACTTATTTTTTCTTTGTAGCGTTATGGATCCAAGCCTGTTGAGAGAAAGGGAG T C GTF2E2 Ensembl:ENSG00000197265 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:30653551..30656929;chr8:30653505..30656929;chr8:30653512..30656929;chr8:30653495..30656929 26863196 MeRIP-seq:(Medium) rs749600660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021926 Human_Splice_Rec_963520,Human_Splice_Rec_963540,Human_Splice_Rec_963554,Human_Splice_Rec_963564 RMVar_hsa_circ_12531,RMVar_hsa_circ_295006,RMVar_hsa_circ_73752,RMVar_hsa_circ_67154 110014 RMVar_ID_110014 Human_SNP_ID_357858474 m1A Human chr8 - 30658022 30658022 30658022 GCAGTGCCGGCGTGGGCGGCCGGCCGAGGCGGAGGCGCAGGAAGGGGGCGGCGAGTCGTGCGAGG GCAGTGCCGGCGTGGGCGGCCGGCCGAGGCGGGGGCGCAGGAAGGGGGCGGCGAGTCGTGCGAGG T C GTF2E2 Ensembl:ENSG00000197265 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:30657951..30658185 26863196 MeRIP-seq:(Medium) rs1239665612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995409,Human_RBP_ID_5153883,Human_RBP_ID_9338624,Human_RBP_ID_9406190,Human_RBP_ID_18426815,Human_RBP_ID_22624688,Human_RBP_ID_26359728 Human_Splice_Rec_963519,Human_Splice_Rec_963539 110015 RMVar_ID_110015 Human_SNP_ID_357858477 m1A Human chr8 - 30658028 30658028 30658028 GAGGGTGCAGTGCCGGCGTGGGCGGCCGGCCGAGGCGGAGGCGCAGGAAGGGGGCGGCGAGTCGT GAGGGTGCAGTGCCGGCGTGGGCGGCCGGCCGCGGCGGAGGCGCAGGAAGGGGGCGGCGAGTCGT T G GTF2E2 Ensembl:ENSG00000197265 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:30657951..30658225;chr8:30657983..30658065;chr8:30657940..30658200;chr8:30657927..30658201;chr8:30657941..30658200 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs901289090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4982669,Human_RBP_ID_5153883,Human_RBP_ID_9338624,Human_RBP_ID_9406190,Human_RBP_ID_18426815,Human_RBP_ID_22624689 Human_Splice_Rec_963519,Human_Splice_Rec_963539 110016 RMVar_ID_110016 Human_SNP_ID_357863993 m1A Human chr8 - 30678498 30678498 30678498 AAATTACCCGAGTGTGGTGATGTGCATCTGTAATCTCAGCTACTTGGGAGGCTGAGGTGAGAGGA AAATTACCCGAGTGTGGTGATGTGCATCTGTAGTCTCAGCTACTTGGGAGGCTGAGGTGAGAGGA T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1138092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831224,Human_RBP_ID_17578620,Human_RBP_ID_18389779,Human_RBP_ID_24255464,Human_RBP_ID_26558125 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 110017 RMVar_ID_110017 Human_SNP_ID_357863994 m1A Human chr8 - 30678499 30678499 30678499 AAAATTACCCGAGTGTGGTGATGTGCATCTGTAATCTCAGCTACTTGGGAGGCTGAGGTGAGAGG AAAATTACCCGAGTGTGGTGATGTGCATCTGTGATCTCAGCTACTTGGGAGGCTGAGGTGAGAGG T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1138089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831224,Human_RBP_ID_17578620,Human_RBP_ID_18389779,Human_RBP_ID_24255464,Human_RBP_ID_26558125 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 110018 RMVar_ID_110018 Human_SNP_ID_357864299 m1A Human chr8 - 30679603 30679603 30679603 ATGAAATGCTGCAGGGTTTTGCTGTTGCAGTGAAGATGGGAGCAACGAAGGCAGACTTTGACAAC ATGAAATGCTGCAGGGTTTTGCTGTTGCAGTGCAGATGGGAGCAACGAAGGCAGACTTTGACAAC T G GSR Ensembl:ENSG00000104687 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:30679305..30680938 32194978 MeRIP-seq:(Medium) rs371380535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_698528,Human_RBP_ID_2054798,Human_RBP_ID_5000358,Human_RBP_ID_5123462,Human_RBP_ID_5154246,Human_RBP_ID_7831265,Human_RBP_ID_9224081,Human_RBP_ID_18124853,Human_RBP_ID_24255475,Human_RBP_ID_26832031 Human_Splice_Rec_963606,Human_Splice_Rec_963632,Human_Splice_Rec_963658,Human_Splice_Rec_963678,Human_Splice_Rec_963700,Human_Splice_Rec_963722 Human_miRNA_ID_2214163 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 110019 RMVar_ID_110019 Human_SNP_ID_357866909 m1A Human chr8 - 30689315 30689315 30689315 ATGTGTAACACATTTTATTTGCCAATAGGTCAAGGAGGTTAAAAAGACTTTGTCGGGCTTGGAAG ATGTGTAACACATTTTATTTGCCAATAGGTCAGGGAGGTTAAAAAGACTTTGTCGGGCTTGGAAG T C GSR Ensembl:ENSG00000104687 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:30689264..30696387 32194978 MeRIP-seq:(Medium) rs759091574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22689080,Human_RBP_ID_26832035 Human_Splice_Rec_963598,Human_Splice_Rec_963624,Human_Splice_Rec_963650,Human_Splice_Rec_963714,Human_Splice_Rec_963734 RMVar_hsa_circ_251111,RMVar_hsa_circ_120092,RMVar_hsa_circ_328758,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_349297,RMVar_hsa_circ_251106,RMVar_hsa_circ_356154,RMVar_hsa_circ_291496,RMVar_hsa_circ_305688,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_277103,RMVar_hsa_circ_251112,RMVar_hsa_circ_251114,RMVar_hsa_circ_251109,RMVar_hsa_circ_251110,RMVar_hsa_circ_311544,RMVar_hsa_circ_316740,RMVar_hsa_circ_337358,RMVar_hsa_circ_361217,RMVar_hsa_circ_313640,RMVar_hsa_circ_251116,RMVar_hsa_circ_303087,RMVar_hsa_circ_251115,RMVar_hsa_circ_267311,RMVar_hsa_circ_303799,RMVar_hsa_circ_349314,RMVar_hsa_circ_251113,RMVar_hsa_circ_373280,RMVar_hsa_circ_311585,RMVar_hsa_circ_290023,RMVar_hsa_circ_251118,RMVar_hsa_circ_251119,RMVar_hsa_circ_251117 110020 RMVar_ID_110020 Human_SNP_ID_357870591 m1A Human chr8 - 30703126 30703126 30703126 CCGCCCCACACATCCTGATCGCCACAGGTGGTATGCCCTCCACCCCTCATGAGAGCCAGATCCCC CCGCCCCACACATCCTGATCGCCACAGGTGGTGTGCCCTCCACCCCTCATGAGAGCCAGATCCCC T C GSR Ensembl:ENSG00000104687 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:30703094..30708075 32194978 MeRIP-seq:(Medium) rs758849140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795516,Human_RBP_ID_4982771,Human_RBP_ID_18196718,Human_RBP_ID_26832645 Human_Splice_Rec_963591,Human_Splice_Rec_963617,Human_Splice_Rec_963643,Human_Splice_Rec_963667,Human_Splice_Rec_963687,Human_Splice_Rec_963709,Human_Splice_Rec_963747 Human_miRNA_ID_2153197,Human_miRNA_ID_2695517,Human_miRNA_ID_2801071,Human_miRNA_ID_3009199 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_277103,RMVar_hsa_circ_251112,RMVar_hsa_circ_99877,RMVar_hsa_circ_316740,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_349314,RMVar_hsa_circ_251113,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_352903,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251121,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_338456,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_251127,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_276969,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_102640,RMVar_hsa_circ_378637,RMVar_hsa_circ_251128 110021 RMVar_ID_110021 Human_SNP_ID_357881227 m1A Human chr8 - 30744266 30744266 30744266 AAGGGAAAAAGTCACACTTACCTATATCCGGGATCCCACGCCGGAGCTCCAGACACACAAGGGGG AAGGGAAAAAGTCACACTTACCTATATCCGGGGTCCCACGCCGGAGCTCCAGACACACAAGGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:30744216..30744401 26863196 MeRIP-seq:(Medium) rs1258272638 Functional Loss SNV dbSNP153 33..33 33 - - - 110022 RMVar_ID_110022 Human_SNP_ID_357893829 m1A Human chr8 - 30791308 30791308 30791308 TAATGAATTTGTTTTTATCCTGCAGGGATACAATTGGTGTCATGATCGGAATGTGGTTACCATTT TAATGAATTTGTTTTTATCCTGCAGGGATACAGTTGGTGTCATGATCGGAATGTGGTTACCATTT T C PPP2CB Ensembl:ENSG00000104695 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:30791257..30791357 32194978 MeRIP-seq:(Medium) rs1296593420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_698577,Human_RBP_ID_8919078 Human_Splice_Rec_963864,Human_Splice_Rec_963874 RMVar_hsa_circ_30390,RMVar_hsa_circ_251131,RMVar_hsa_circ_81964,RMVar_hsa_circ_372941,RMVar_hsa_circ_251132,RMVar_hsa_circ_377620,RMVar_hsa_circ_302638,RMVar_hsa_circ_251133,RMVar_hsa_circ_251134 110023 RMVar_ID_110023 Human_SNP_ID_357896133 m1A Human chr8 - 30799752 30799752 30799752 TGTAATTGTTGATTTCACTTTTCTAACAGGCAAAGGAAATTTTAACAAAAGAATCAAATGTGCAA TGTAATTGTTGATTTCACTTTTCTAACAGGCAGAGGAAATTTTAACAAAAGAATCAAATGTGCAA T C PPP2CB Ensembl:ENSG00000104695 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:30799701..30799775 26863196 MeRIP-seq:(Medium) rs144505371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18124591 Human_Splice_Rec_963852,Human_Splice_Rec_963853,Human_Splice_Rec_963856,Human_Splice_Rec_963886,Human_Splice_Rec_963892 RMVar_hsa_circ_251132,RMVar_hsa_circ_377620,RMVar_hsa_circ_302638,RMVar_hsa_circ_251134,RMVar_hsa_circ_292195,RMVar_hsa_circ_348013 110024 RMVar_ID_110024 Human_SNP_ID_357899613 m1A Human chr8 - 30812370 30812370 30812370 CCAAGGAGCTGGACCAGTGGGTCGAGCAGCTGAACGAGTGTAAGCAGCTGAACGAGAACCAAGTG CCAAGGAGCTGGACCAGTGGGTCGAGCAGCTGGACGAGTGTAAGCAGCTGAACGAGAACCAAGTG T C PPP2CB Ensembl:ENSG00000104695 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:30810220..30812413 32194978 MeRIP-seq:(Medium) rs1360383752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3877594,Human_RBP_ID_4995415,Human_RBP_ID_8222738,Human_RBP_ID_24255579 Human_Splice_Rec_963851,Human_Splice_Rec_963855 110025 RMVar_ID_110025 Human_SNP_ID_357899773 m1A Human chr8 - 30812679 30812679 30812679 CGCTCCCCGGCACCTCACCGCGTCCTTCACCGACTCCCGCGGCGCGCGGCCGGGCGGGGAAGGGC CGCTCCCCGGCACCTCACCGCGTCCTTCACCGGCTCCCGCGGCGCGCGGCCGGGCGGGGAAGGGC T C PPP2CB Ensembl:ENSG00000104695 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:30812326..30812825 26863196 MeRIP-seq:(Medium) rs1450275846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15063,Human_RBP_ID_4996030,Human_RBP_ID_5430406,Human_RBP_ID_5453436,Human_RBP_ID_5480973,Human_RBP_ID_5514751,Human_RBP_ID_9354923,Human_RBP_ID_24255580 110026 RMVar_ID_110026 Human_SNP_ID_357899806 m1A Human chr8 + 30812767 30812767 30812767 CTCGCCGGACGAAGGCCGCCCGCTGCCGCTTCAGGCCCGCCTCACGCCTACCGGCCTCTCCCGAC CTCGCCGGACGAAGGCCGCCCGCTGCCGCTTCTGGCCCGCCTCACGCCTACCGGCCTCTCCCGAC A T RF00017-4500 RNACentral:URS000099DB47 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:30812301..30812825 26863196 MeRIP-seq:(Medium) rs759047850 Functional Loss SNV dbSNP153 33..33 33 - - - 110027 RMVar_ID_110027 Human_SNP_ID_357899823 m1A Human chr8 + 30812784 30812784 30812784 GCCCGCTGCCGCTTCAGGCCCGCCTCACGCCTACCGGCCTCTCCCGACTTGTCTTTCCCCTTCTC GCCCGCTGCCGCTTCAGGCCCGCCTCACGCCTGCCGGCCTCTCCCGACTTGTCTTTCCCCTTCTC A G RF00017-4500 RNACentral:URS000099DB47 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:30812301..30812859 26863196 MeRIP-seq:(Medium) rs1214440717 Functional Loss SNV dbSNP153 33..33 33 - - - 110028 RMVar_ID_110028 Human_SNP_ID_357899837 m1A Human chr8 - 30812801 30812801 30812801 GGGGAGAGAAAGAGCGAGAGAAGGGGAAAGACAAGTCGGGAGAGGCCGGTAGGCGTGAGGCGGGC GGGGAGAGAAAGAGCGAGAGAAGGGGAAAGACGAGTCGGGAGAGGCCGGTAGGCGTGAGGCGGGC T C PPP2CB Ensembl:ENSG00000104695 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:30812655..30812825 26863196 MeRIP-seq:(Medium) rs1397602072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796728,Human_RBP_ID_3885269,Human_RBP_ID_5000427,Human_RBP_ID_5453438,Human_RBP_ID_5480974,Human_RBP_ID_9440854,Human_RBP_ID_18426677 Human_Splice_Rec_963877 110029 RMVar_ID_110029 Human_SNP_ID_357956687 m1A Human chr8 + 31035441 31035441 31035441 GGAGGAGAAGAAAGTACAAAGGCCCTGGGGGAACCTGCCTCTTTATGTTCAGAGAGCAACTTAAG GGAGGAGAAGAAAGTACAAAGGCCCTGGGGGAGCCTGCCTCTTTATGTTCAGAGAGCAACTTAAG A G WRN Ensembl:ENSG00000165392 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:31035421..31035593 26863196 MeRIP-seq:(Medium) rs928521686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831664 110030 RMVar_ID_110030 Human_SNP_ID_357958039 m1A Human chr8 - 31041738 31041738 31041738 ACTACTTCCTGGCAATCCTACAACTTTTCCCTAATCTATTTACTATCCTCCCCTCCTAAGACTAT ACTACTTCCTGGCAATCCTACAACTTTTCCCTTATCTATTTACTATCCTCCCCTCCTAAGACTAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:31041692..31041776 26863196 MeRIP-seq:(Medium) rs35529280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15326,GWAS_ID_15327,GWAS_ID_15328,GWAS_ID_15329,GWAS_ID_15330 110031 RMVar_ID_110031 Human_SNP_ID_357958040 m1A Human chr8 - 31041738 31041738 31041738 ACTACTTCCTGGCAATCCTACAACTTTTCCCTAATCTATTTACTATCCTCCCCTCCTAAGACTAT ACTACTTCCTGGCAATCCTACAACTTTTCCCTGATCTATTTACTATCCTCCCCTCCTAAGACTAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:31041692..31041776 26863196 MeRIP-seq:(Medium) rs35529280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15326,GWAS_ID_15327,GWAS_ID_15328,GWAS_ID_15329,GWAS_ID_15330 110032 RMVar_ID_110032 Human_SNP_ID_357958041 m1A Human chr8 - 31041738 31041738 31041738 ACTACTTCCTGGCAATCCTACAACTTTTCCCTAATCTATTTACTATCCTCCCCTCCTAAGACTAT ACTACTTCCTGGCAATCCTACAACTTTTCCCTCATCTATTTACTATCCTCCCCTCCTAAGACTAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:31041692..31041776 26863196 MeRIP-seq:(Medium) rs35529280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15326,GWAS_ID_15327,GWAS_ID_15328,GWAS_ID_15329,GWAS_ID_15330 110033 RMVar_ID_110033 Human_SNP_ID_357958119 m1A Human chr8 - 31042170 31042170 31042170 TACTATGTTATTACCAACGACTGAATCCTTCCATAATCTCAATTCCATATATCCCACTCTCCAAC TACTATGTTATTACCAACGACTGAATCCTTCCGTAATCTCAATTCCATATATCCCACTCTCCAAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:31042154..31042269 26863196 MeRIP-seq:(Medium) rs890899118 Functional Loss SNV dbSNP153 33..33 33 - - - 110034 RMVar_ID_110034 Human_SNP_ID_357965451 m1A Human chr8 + 31073721 31073721 31073721 CCAGCATTTAGAGGTTGGGAAGATGAGGAGAGAGCAGCAAAGAGGACTGGGAGGGCCACTAATGA CCAGCATTTAGAGGTTGGGAAGATGAGGAGAGGGCAGCAAAGAGGACTGGGAGGGCCACTAATGA A G WRN Ensembl:ENSG00000165392 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:31073609..31073830 26863196 MeRIP-seq:(Medium) rs1254334578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14757,Human_RBP_ID_845062,Human_RBP_ID_7831858 RMVar_hsa_circ_11004,RMVar_hsa_circ_50811,RMVar_hsa_circ_335697,RMVar_hsa_circ_352692,RMVar_hsa_circ_340300,RMVar_hsa_circ_323219,RMVar_hsa_circ_302547,RMVar_hsa_circ_53091,RMVar_hsa_circ_39525,RMVar_hsa_circ_12721,RMVar_hsa_circ_6133,RMVar_hsa_circ_8417,RMVar_hsa_circ_64871,RMVar_hsa_circ_251142,RMVar_hsa_circ_251143,RMVar_hsa_circ_251144,RMVar_hsa_circ_326757,RMVar_hsa_circ_337022,RMVar_hsa_circ_339613,RMVar_hsa_circ_329260,RMVar_hsa_circ_72571,RMVar_hsa_circ_24285,RMVar_hsa_circ_53848,RMVar_hsa_circ_126797,RMVar_hsa_circ_251146,RMVar_hsa_circ_251147,RMVar_hsa_circ_251145,RMVar_hsa_circ_66314,RMVar_hsa_circ_23272,RMVar_hsa_circ_43449,RMVar_hsa_circ_251148 110035 RMVar_ID_110035 Human_SNP_ID_357965452 m1A Human chr8 + 31073724 31073724 31073724 GCATTTAGAGGTTGGGAAGATGAGGAGAGAGCAGCAAAGAGGACTGGGAGGGCCACTAATGAAGG GCATTTAGAGGTTGGGAAGATGAGGAGAGAGCCGCAAAGAGGACTGGGAGGGCCACTAATGAAGG A C WRN Ensembl:ENSG00000165392 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:31073580..31073834 26863196 MeRIP-seq:(Medium) rs1420237590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14757,Human_RBP_ID_845062 RMVar_hsa_circ_11004,RMVar_hsa_circ_50811,RMVar_hsa_circ_335697,RMVar_hsa_circ_352692,RMVar_hsa_circ_340300,RMVar_hsa_circ_323219,RMVar_hsa_circ_302547,RMVar_hsa_circ_53091,RMVar_hsa_circ_39525,RMVar_hsa_circ_12721,RMVar_hsa_circ_6133,RMVar_hsa_circ_8417,RMVar_hsa_circ_64871,RMVar_hsa_circ_251142,RMVar_hsa_circ_251143,RMVar_hsa_circ_251144,RMVar_hsa_circ_326757,RMVar_hsa_circ_337022,RMVar_hsa_circ_339613,RMVar_hsa_circ_329260,RMVar_hsa_circ_72571,RMVar_hsa_circ_24285,RMVar_hsa_circ_53848,RMVar_hsa_circ_126797,RMVar_hsa_circ_251146,RMVar_hsa_circ_251147,RMVar_hsa_circ_251145,RMVar_hsa_circ_66314,RMVar_hsa_circ_23272,RMVar_hsa_circ_43449,RMVar_hsa_circ_251148 110036 RMVar_ID_110036 Human_SNP_ID_357965453 m1A Human chr8 + 31073724 31073724 31073724 GCATTTAGAGGTTGGGAAGATGAGGAGAGAGCAGCAAAGAGGACTGGGAGGGCCACTAATGAAGG GCATTTAGAGGTTGGGAAGATGAGGAGAGAGCGGCAAAGAGGACTGGGAGGGCCACTAATGAAGG A G WRN Ensembl:ENSG00000165392 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:31073580..31073834 26863196 MeRIP-seq:(Medium) rs1420237590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14757,Human_RBP_ID_845062 RMVar_hsa_circ_11004,RMVar_hsa_circ_50811,RMVar_hsa_circ_335697,RMVar_hsa_circ_352692,RMVar_hsa_circ_340300,RMVar_hsa_circ_323219,RMVar_hsa_circ_302547,RMVar_hsa_circ_53091,RMVar_hsa_circ_39525,RMVar_hsa_circ_12721,RMVar_hsa_circ_6133,RMVar_hsa_circ_8417,RMVar_hsa_circ_64871,RMVar_hsa_circ_251142,RMVar_hsa_circ_251143,RMVar_hsa_circ_251144,RMVar_hsa_circ_326757,RMVar_hsa_circ_337022,RMVar_hsa_circ_339613,RMVar_hsa_circ_329260,RMVar_hsa_circ_72571,RMVar_hsa_circ_24285,RMVar_hsa_circ_53848,RMVar_hsa_circ_126797,RMVar_hsa_circ_251146,RMVar_hsa_circ_251147,RMVar_hsa_circ_251145,RMVar_hsa_circ_66314,RMVar_hsa_circ_23272,RMVar_hsa_circ_43449,RMVar_hsa_circ_251148 110037 RMVar_ID_110037 Human_SNP_ID_357965720 m1A Human chr8 + 31074809 31074809 31074809 GATTACTGTAATGTGGGTAAGAGAGGAATGGAAGGCTCAGTGGGCAGTGGGAGTAGGGATGTTGA GATTACTGTAATGTGGGTAAGAGAGGAATGGAGGGCTCAGTGGGCAGTGGGAGTAGGGATGTTGA A G WRN Ensembl:ENSG00000165392 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:31074734..31075348 26863196 MeRIP-seq:(Medium) rs1027783802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831870 RMVar_hsa_circ_11004,RMVar_hsa_circ_50811,RMVar_hsa_circ_335697,RMVar_hsa_circ_352692,RMVar_hsa_circ_340300,RMVar_hsa_circ_323219,RMVar_hsa_circ_302547,RMVar_hsa_circ_53091,RMVar_hsa_circ_39525,RMVar_hsa_circ_12721,RMVar_hsa_circ_6133,RMVar_hsa_circ_8417,RMVar_hsa_circ_64871,RMVar_hsa_circ_251142,RMVar_hsa_circ_251143,RMVar_hsa_circ_251144,RMVar_hsa_circ_326757,RMVar_hsa_circ_337022,RMVar_hsa_circ_339613,RMVar_hsa_circ_329260,RMVar_hsa_circ_72571,RMVar_hsa_circ_24285,RMVar_hsa_circ_53848,RMVar_hsa_circ_126797,RMVar_hsa_circ_251146,RMVar_hsa_circ_251147,RMVar_hsa_circ_251145,RMVar_hsa_circ_66314,RMVar_hsa_circ_23272,RMVar_hsa_circ_43449,RMVar_hsa_circ_251148 110038 RMVar_ID_110038 Human_SNP_ID_358437465 m1A Human chr8 + 33013304 33013304 33013304 GGCAAATCTTGTCCCGCCTATTTACCAAAAACATCACCTCTAGCATTACCAGTATTAGAGGCACT GGCAAATCTTGTCCCGCCTATTTACCAAAAACGTCACCTCTAGCATTACCAGTATTAGAGGCACT A G AC090204.1 Ensembl:ENSG00000247134 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:33013251..33013391 26863196 MeRIP-seq:(Medium) rs1295321383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8274260,Human_RBP_ID_18117673 110039 RMVar_ID_110039 Human_SNP_ID_358551949 m1A Human chr8 - 33484787 33484787 33484787 GGGCCTCCCCTCTGCTGGGAGGAGGCTGGGGAAAGCTGCAGGCGGCGCGGCGGGGCTGGGTCCCC GGGCCTCCCCTCTGCTGGGAGGAGGCTGGGGAGAGCTGCAGGCGGCGCGGCGGGGCTGGGTCCCC T C TTI2 Ensembl:ENSG00000129696 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:33484736..33484850 26863196 MeRIP-seq:(Medium) rs1273730647 Functional Loss SNV dbSNP153 33..33 33 - - - 110040 RMVar_ID_110040 Human_SNP_ID_358559353 m1A Human chr8 - 33512339 33512339 33512339 ACTGGGGCAGGTAGCAAAAGCCCTGGAGAAGTATGCAGCCCCCTCCAAGGAGGAGGAAGGTGGAG ACTGGGGCAGGTAGCAAAAGCCCTGGAGAAGTGTGCAGCCCCCTCCAAGGAGGAGGAAGGTGGAG T C TTI2 Ensembl:ENSG00000129696 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:33512160..33512360 32194978 MeRIP-seq:(Medium) rs1306487105 Functional Loss SNV dbSNP153 33..33 33 - - - 110041 RMVar_ID_110041 Human_SNP_ID_358559510 m1A Human chr8 + 33512656 33512656 33512656 AGCACCAGAAGGCTGGTCTCTCCCACAGAACGAGGATGGAGGCGGGGAGGGATCCGTTGAAGAGG AGCACCAGAAGGCTGGTCTCTCCCACAGAACGCGGATGGAGGCGGGGAGGGATCCGTTGAAGAGG A C RF00017-4567 RNACentral:URS000093B3AD SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:33512607..33512757 32194978 MeRIP-seq:(Medium) rs188801575 Functional Loss SNV dbSNP153 33..33 33 - - - 110042 RMVar_ID_110042 Human_SNP_ID_358559964 m1A Human chr8 + 33513535 33513535 33513535 TTGGGTGTTCATACGCTTGTGTGAGATGTGCCACCCTTGAACCTTGTTACGACGTGGGCACATTA TTGGGTGTTCATACGCTTGTGTGAGATGTGCCCCCCTTGAACCTTGTTACGACGTGGGCACATTA A C SNORD13 Ensembl:ENSG00000239039 snoRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:33513476..33513575 26863196 MeRIP-seq:(Medium) rs11785250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961286,Human_RBP_ID_1117551,Human_RBP_ID_1224421,Human_RBP_ID_1335782,Human_RBP_ID_1696119,Human_RBP_ID_2054937,Human_RBP_ID_3877768,Human_RBP_ID_4983340,Human_RBP_ID_5090916,Human_RBP_ID_5106869,Human_RBP_ID_5223328,Human_RBP_ID_5480983,Human_RBP_ID_5514765,Human_RBP_ID_5536151,Human_RBP_ID_5629051,Human_RBP_ID_5658450,Human_RBP_ID_8274009,Human_RBP_ID_8686254,Human_RBP_ID_8731083,Human_RBP_ID_8919280,Human_RBP_ID_9224266,Human_RBP_ID_9264351,Human_RBP_ID_10395113,Human_RBP_ID_17065460,Human_RBP_ID_17201580,Human_RBP_ID_17579033,Human_RBP_ID_17672432,Human_RBP_ID_17715411,Human_RBP_ID_18174280,Human_RBP_ID_18426681,Human_RBP_ID_18520835,Human_RBP_ID_18541464,Human_RBP_ID_18896024,Human_RBP_ID_18927532,Human_RBP_ID_21612405,Human_RBP_ID_22368049,Human_RBP_ID_22372540,Human_RBP_ID_22410000,Human_RBP_ID_22425932,Human_RBP_ID_22836820,Human_RBP_ID_23085626,Human_RBP_ID_23110885,Human_RBP_ID_23140812,Human_RBP_ID_24256330,Human_RBP_ID_24440914,Human_RBP_ID_24521389,Human_RBP_ID_24549486,Human_RBP_ID_26168457,Human_RBP_ID_26555470,Human_RBP_ID_26795832,Human_RBP_ID_27538137 Human_miRNA_ID_3142329 110043 RMVar_ID_110043 Human_SNP_ID_358559965 m1A Human chr8 + 33513535 33513535 33513535 TTGGGTGTTCATACGCTTGTGTGAGATGTGCCACCCTTGAACCTTGTTACGACGTGGGCACATTA TTGGGTGTTCATACGCTTGTGTGAGATGTGCCGCCCTTGAACCTTGTTACGACGTGGGCACATTA A G SNORD13 Ensembl:ENSG00000239039 snoRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:33513476..33513575 26863196 MeRIP-seq:(Medium) rs11785250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961286,Human_RBP_ID_1117551,Human_RBP_ID_1224421,Human_RBP_ID_1335782,Human_RBP_ID_1696119,Human_RBP_ID_2054937,Human_RBP_ID_3877768,Human_RBP_ID_4983340,Human_RBP_ID_5090916,Human_RBP_ID_5106869,Human_RBP_ID_5223328,Human_RBP_ID_5480983,Human_RBP_ID_5514765,Human_RBP_ID_5536151,Human_RBP_ID_5629051,Human_RBP_ID_5658450,Human_RBP_ID_8274009,Human_RBP_ID_8686254,Human_RBP_ID_8731083,Human_RBP_ID_8919280,Human_RBP_ID_9224266,Human_RBP_ID_9264351,Human_RBP_ID_10395113,Human_RBP_ID_17065460,Human_RBP_ID_17201580,Human_RBP_ID_17579033,Human_RBP_ID_17672432,Human_RBP_ID_17715411,Human_RBP_ID_18174280,Human_RBP_ID_18426681,Human_RBP_ID_18520835,Human_RBP_ID_18541464,Human_RBP_ID_18896024,Human_RBP_ID_18927532,Human_RBP_ID_21612405,Human_RBP_ID_22368049,Human_RBP_ID_22372540,Human_RBP_ID_22410000,Human_RBP_ID_22425932,Human_RBP_ID_22836820,Human_RBP_ID_23085626,Human_RBP_ID_23110885,Human_RBP_ID_23140812,Human_RBP_ID_24256330,Human_RBP_ID_24440914,Human_RBP_ID_24521389,Human_RBP_ID_24549486,Human_RBP_ID_26168457,Human_RBP_ID_26555470,Human_RBP_ID_26795832,Human_RBP_ID_27538137 Human_miRNA_ID_3142329 110044 RMVar_ID_110044 Human_SNP_ID_358559992 m1A Human chr8 - 33513546 33513546 33513546 GGTCAGACGGGTAATGTGCCCACGTCGTAACAAGGTTCAAGGGTGGCACATCTCACACAAGCGTA GGTCAGACGGGTAATGTGCCCACGTCGTAACATGGTTCAAGGGTGGCACATCTCACACAAGCGTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:33513495..33513561 26863196 MeRIP-seq:(Medium) rs773860067 Functional Loss SNV dbSNP153 33..33 33 - - - 110045 RMVar_ID_110045 Human_SNP_ID_358559993 m1A Human chr8 - 33513546 33513546 33513546 GGTCAGACGGGTAATGTGCCCACGTCGTAACAAGGTTCAAGGGTGGCACATCTCACACAAGCGTA GGTCAGACGGGTAATGTGCCCACGTCGTAACAGGGTTCAAGGGTGGCACATCTCACACAAGCGTA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:33513495..33513561 26863196 MeRIP-seq:(Medium) rs773860067 Functional Loss SNV dbSNP153 33..33 33 - - - 110046 RMVar_ID_110046 Human_SNP_ID_358559994 m1A Human chr8 - 33513546 33513546 33513546 GGTCAGACGGGTAATGTGCCCACGTCGTAACAAGGTTCAAGGGTGGCACATCTCACACAAGCGTA GGTCAGACGGGTAATGTGCCCACGTCGTAACACGGTTCAAGGGTGGCACATCTCACACAAGCGTA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:33513495..33513561 26863196 MeRIP-seq:(Medium) rs773860067 Functional Loss SNV dbSNP153 33..33 33 - - - 110047 RMVar_ID_110047 Human_SNP_ID_358574297 m1A Human chr8 - 33567028 33567028 33567028 TTTTCCCTCCTCCCCCGGCCGAGGGCTTCTGCAGCCCGGGCACCCCCGCCCCGCGGCGCCCCACA TTTTCCCTCCTCCCCCGGCCGAGGGCTTCTGCCGCCCGGGCACCCCCGCCCCGCGGCGCCCCACA T G RNF122 Ensembl:ENSG00000133874 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:33566927..33567100 26863410 MeRIP-seq:(Medium) rs3735952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4994988 110048 RMVar_ID_110048 Human_SNP_ID_359259319 m1A Human chr8 + 36300160 36300160 36300160 TTTCCAAATTTGTTTCTATATAACATTTATATACATTATCTGTACATGTAAATTGAACTACATAA TTTCCAAATTTGTTTCTATATAACATTTATATGCATTATCTGTACATGTAAATTGAACTACATAA A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:36300131..36300215 26863410 MeRIP-seq:(Medium) rs1412182225 Functional Loss SNV dbSNP153 33..33 33 - - - 110049 RMVar_ID_110049 Human_SNP_ID_359259320 m1A Human chr8 + 36300160 36300160 36300160 TTTCCAAATTTGTTTCTATATAACATTTATATACATTATCTGTACATGTAAATTGAACTACATAA TTTCCAAATTTGTTTCTATATAACATTTATATTCATTATCTGTACATGTAAATTGAACTACATAA A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr8:36300131..36300215 26863410 MeRIP-seq:(Medium) rs1412182225 Functional Loss SNV dbSNP153 33..33 33 - - - 110050 RMVar_ID_110050 Human_SNP_ID_359590052 m1A Human chr8 + 37598465 37598465 37598465 AAGGAAAAGGCACACAAGGTCCCCCAGCCCCCACACACAGAGGAGCCACACCTGCACCCCTCCCT AAGGAAAAGGCACACAAGGTCCCCCAGCCCCCCCACACAGAGGAGCCACACCTGCACCCCTCCCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:37598414..37598501 26863196 MeRIP-seq:(Medium) rs909195869 Functional Loss SNV dbSNP153 33..33 33 - - - 110051 RMVar_ID_110051 Human_SNP_ID_359613601 m1A Human chr8 + 37695845 37695833 37695845 GGTGGCGGCGGCGGCGGAGGCGTCGGTGGAGGAGGGGAGGCGGCGAGGAGGCGCAGCTCCCGCTG GGTGGCGGCGGCGGCGGAGGC____________GGGGAGGCGGCGAGGAGGCGCAGCTCCCGCTG CGTCGGTGGAGGA C ZNF703 Ensembl:ENSG00000183779 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:37695798..37695914 26863196 MeRIP-seq:(Medium) rs1445674573 Functional Loss DEL dbSNP153 22..33 33 - - - Human_RBP_ID_255533,Human_RBP_ID_4996036,Human_RBP_ID_5453463,Human_RBP_ID_7833573,Human_RBP_ID_8274012,Human_RBP_ID_8919286 110052 RMVar_ID_110052 Human_SNP_ID_359613618 m1A Human chr8 - 37695876 37695876 37695876 GTGGGCTCGCTCCGCAGCGTCGATCGCGGTGCAGCGGGAGCTGCGCCTCCTCGCCGCCTCCCCTC GTGGGCTCGCTCCGCAGCGTCGATCGCGGTGCCGCGGGAGCTGCGCCTCCTCGCCGCCTCCCCTC T G lnc-BRF2-3 RNACentral:URS0000D5C499 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:37695776..37695950 26863410 MeRIP-seq:(Medium) rs1199174177 Functional Loss SNV dbSNP153 33..33 33 - - - 110053 RMVar_ID_110053 Human_SNP_ID_359613752 m1A Human chr8 - 37696167 37696167 37696167 AGGACAGCGGCTGCAGGTACTCCGGGTGCAGGAGGTGACCGGTGTGAGCGCTCAGCATCTTCAGG AGGACAGCGGCTGCAGGTACTCCGGGTGCAGGTGGTGACCGGTGTGAGCGCTCAGCATCTTCAGG T A lnc-BRF2-3 RNACentral:URS0000D5C499 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:37696000..37697173 26863196 MeRIP-seq:(Medium) rs541607232 Functional Loss SNV dbSNP153 33..33 33 - - - 110054 RMVar_ID_110054 Human_SNP_ID_359614320 m1A Human chr8 - 37697792 37697792 37697792 AGCGGGAACACCGAGTGGCCCGGCTTGTAGGGAGACACCGGCGCCACGTGGCCGGCCCCCACCAG AGCGGGAACACCGAGTGGCCCGGCTTGTAGGGCGACACCGGCGCCACGTGGCCGGCCCCCACCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:37697743..37697847 26863196 MeRIP-seq:(Medium) rs1485171089 Functional Loss SNV dbSNP153 33..33 33 - - - 110055 RMVar_ID_110055 Human_SNP_ID_359614504 m1A Human chr8 - 37698184 37698184 37698184 CGGGGAGCGCGGCCTGGGCGGCGCTGGACGAGAGCGCGGCGGGCTGCAGCGGGTGCCCGGGGTAC CGGGGAGCGCGGCCTGGGCGGCGCTGGACGAGGGCGCGGCGGGCTGCAGCGGGTGCCCGGGGTAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:37697721..37698372 32194978 MeRIP-seq:(Medium) rs1427359449 Functional Loss SNV dbSNP153 33..33 33 - - - 110056 RMVar_ID_110056 Human_SNP_ID_359614666 m1A Human chr8 - 37698496 37698496 37698496 TTAGGCCCAAAGTGTGTGGATTCCGCAAGGACAGCGACCCGGGGCTGCCGGGGGCGGCGGGCGGG TTAGGCCCAAAGTGTGTGGATTCCGCAAGGACTGCGACCCGGGGCTGCCGGGGGCGGCGGGCGGG T A - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:37698398..37698495 26863410 MeRIP-seq:(Medium) rs763865868 Functional Loss SNV dbSNP153 33..33 33 - - - 110057 RMVar_ID_110057 Human_SNP_ID_359615070 m1A Human chr8 - 37699840 37699840 37699840 GTCCACTCTGGGGGCTCTGCCGGGCCAGGCCTAGGAGAGGGCGGGGGCTGCTGTGATCCGAGAGC GTCCACTCTGGGGGCTCTGCCGGGCCAGGCCTGGGAGAGGGCGGGGGCTGCTGTGATCCGAGAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr8:37699793..37699867;chr8:37699764..37699877 26863196 MeRIP-seq:(Medium) rs1207006593 Functional Loss SNV dbSNP153 33..33 33 - - - 110058 RMVar_ID_110058 Human_SNP_ID_359625658 m1A Human chr8 + 37740316 37740316 37740316 GAAAGTTGACCCTCATGATATTGATCTAACAGAGCCTTCTTGCCAAACTGAAGCTGCCTCTCTCT GAAAGTTGACCCTCATGATATTGATCTAACAGTGCCTTCTTGCCAAACTGAAGCTGCCTCTCTCT A T ERLIN2 Ensembl:ENSG00000147475 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:37740313..37740386 26863196 MeRIP-seq:(Medium) rs775831501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42881,RMVar_hsa_circ_299691 110059 RMVar_ID_110059 Human_SNP_ID_359627996 m1A Human chr8 + 37749815 37749815 37749815 TCTCTCTCCAGGCTGTGCGGGTAACAAAGCCCAACATACCAGAGGCAATCCGCAGAAACTACGAG TCTCTCTCCAGGCTGTGCGGGTAACAAAGCCCCACATACCAGAGGCAATCCGCAGAAACTACGAG A C ERLIN2 Ensembl:ENSG00000147475 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:37749576..37749838 32194978 MeRIP-seq:(Medium) rs1258969957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22776043,Human_RBP_ID_23085673 Human_Splice_Rec_965560,Human_Splice_Rec_965561,Human_Splice_Rec_965600,Human_Splice_Rec_965601,Human_Splice_Rec_965620,Human_Splice_Rec_965656,Human_Splice_Rec_965657 RMVar_hsa_circ_34493 110060 RMVar_ID_110060 Human_SNP_ID_359631085 m1A Human chr8 + 37762675 37762675 37762675 GCGTCGGTCCCCGGGGGATGTGGAGAGCTGGCAGCATGTCGGCCGAGCTGGGAGTCGGGTGCGCA GCGTCGGTCCCCGGGGGATGTGGAGAGCTGGCCGCATGTCGGCCGAGCTGGGAGTCGGGTGCGCA A C PLPBP Ensembl:ENSG00000147471 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:37762625..37765600;chr8:37762626..37765559 26863196 MeRIP-seq:(Medium) rs568414778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995427,Human_RBP_ID_23140842 Human_Splice_Rec_965679,Human_Splice_Rec_965685,Human_Splice_Rec_965693,Human_Splice_Rec_965703,Human_Splice_Rec_965709,Human_Splice_Rec_965723 110061 RMVar_ID_110061 Human_SNP_ID_359631086 m1A Human chr8 + 37762675 37762675 37762675 GCGTCGGTCCCCGGGGGATGTGGAGAGCTGGCAGCATGTCGGCCGAGCTGGGAGTCGGGTGCGCA GCGTCGGTCCCCGGGGGATGTGGAGAGCTGGCGGCATGTCGGCCGAGCTGGGAGTCGGGTGCGCA A G PLPBP Ensembl:ENSG00000147471 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:37762625..37765600;chr8:37762626..37765559 26863196 MeRIP-seq:(Medium) rs568414778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995427,Human_RBP_ID_23140842 Human_Splice_Rec_965679,Human_Splice_Rec_965685,Human_Splice_Rec_965693,Human_Splice_Rec_965703,Human_Splice_Rec_965709,Human_Splice_Rec_965723 110062 RMVar_ID_110062 Human_SNP_ID_359631092 m1A Human chr8 - 37762681 37762681 37762681 CCGCAATGCGCACCCGACTCCCAGCTCGGCCGACATGCTGCCAGCTCTCCACATCCCCCGGGGAC CCGCAATGCGCACCCGACTCCCAGCTCGGCCGGCATGCTGCCAGCTCTCCACATCCCCCGGGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:37762636..37765559 26863196 MeRIP-seq:(Medium) rs1368188716 Functional Loss SNV dbSNP153 33..33 33 - - - 110063 RMVar_ID_110063 Human_SNP_ID_359631132 m1A Human chr8 - 37762742 37762742 37762742 CAGCCTCCTTCCTCACCCGCGGCCGCCGCGCCACAGCCTGCTGCACGCGCTCGTTCACCGCCCGC CAGCCTCCTTCCTCACCCGCGGCCGCCGCGCCGCAGCCTGCTGCACGCGCTCGTTCACCGCCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:37762642..37765559 26863410 MeRIP-seq:(Medium) rs1399840137 Functional Loss SNV dbSNP153 33..33 33 - - - 110064 RMVar_ID_110064 Human_SNP_ID_359653534 m1A Human chr8 - 37844796 37844796 37844796 GTCCGCTCTGCCTTTCGGGATGGGACAGCAGAAGTGGAGACCCGAGAGAAGGAGCCACCGGGGTG GTCCGCTCTGCCTTTCGGGATGGGACAGCAGAGGTGGAGACCCGAGAGAAGGAGCCACCGGGGTG T C BRF2 Ensembl:ENSG00000104221 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:37844745..37844855 26863196 MeRIP-seq:(Medium) rs775407636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22114913 RMVar_hsa_circ_95570,RMVar_hsa_circ_251321 110065 RMVar_ID_110065 Human_SNP_ID_359653571 m1A Human chr8 + 37844874 37844874 37844874 TGCTGGAGAAGGTCACCGATGTGCTTCACCACAGACCGTTTGTCAAGTCTCAGAACTCGTAACCA TGCTGGAGAAGGTCACCGATGTGCTTCACCACGGACCGTTTGTCAAGTCTCAGAACTCGTAACCA A G ADGRA2 Ensembl:ENSG00000020181 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:37844752..37844881 26863196 MeRIP-seq:(Medium) rs758382548 Functional Loss SNV dbSNP153 33..33 33 - - - 110066 RMVar_ID_110066 Human_SNP_ID_359653572 m1A Human chr8 + 37844874 37844874 37844874 TGCTGGAGAAGGTCACCGATGTGCTTCACCACAGACCGTTTGTCAAGTCTCAGAACTCGTAACCA TGCTGGAGAAGGTCACCGATGTGCTTCACCACTGACCGTTTGTCAAGTCTCAGAACTCGTAACCA A T ADGRA2 Ensembl:ENSG00000020181 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:37844752..37844881 26863196 MeRIP-seq:(Medium) rs758382548 Functional Loss SNV dbSNP153 33..33 33 - - - 110067 RMVar_ID_110067 Human_SNP_ID_359655090 m1A Human chr8 - 37849772 37849772 37849772 GGCTTTGGGGCCGGTTGTGAGATGCCAGGCAGAGGCCGCTGCCCGGACTGCGGCTCCACGGAGCT GGCTTTGGGGCCGGTTGTGAGATGCCAGGCAGTGGCCGCTGCCCGGACTGCGGCTCCACGGAGCT T A BRF2 Ensembl:ENSG00000104221 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:37849723..37849813 26863196 MeRIP-seq:(Medium) rs747323454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995429,Human_RBP_ID_8923434,Human_RBP_ID_17714739,Human_RBP_ID_18118080 RMVar_hsa_circ_119654,RMVar_hsa_circ_251323 110068 RMVar_ID_110068 Human_SNP_ID_359657668 m1A Human chr8 + 37860398 37860398 37860398 AGAGTCTCGCCCGTTGCCCAGGCTGGAGTGCAATGATGTGATCTCAGCTCACTGCAACCTCCACC AGAGTCTCGCCCGTTGCCCAGGCTGGAGTGCAGTGATGTGATCTCAGCTCACTGCAACCTCCACC A G AC130304.1 Ensembl:ENSG00000280064 Other exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:37860140..37860439 32194978 MeRIP-seq:(Medium) rs1159091793 Functional Loss SNV dbSNP153 33..33 33 - - - 110069 RMVar_ID_110069 Human_SNP_ID_359665867 m1A Human chr8 - 37892802 37892802 37892802 TGGGGGCGTGCTTGTGTAAGATGAGGCTGAAGAGGAAGGCGAGGCTTTACTTAGGAGGAATGGTA TGGGGGCGTGCTTGTGTAAGATGAGGCTGAAGTGGAAGGCGAGGCTTTACTTAGGAGGAATGGTA T A RAB11FIP1 Ensembl:ENSG00000156675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:37892790..37892990 26863196 MeRIP-seq:(Medium) rs184375080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7834048 110070 RMVar_ID_110070 Human_SNP_ID_359701277 m1A Human chr8 + 38030571 38030571 38030571 AGCGAGAGGTTCGCGGGTGCAGCGCACAGGAGACCATGTCCGGGGGCAGCAGCTGCAGCCAGACC AGCGAGAGGTTCGCGGGTGCAGCGCACAGGAGGCCATGTCCGGGGGCAGCAGCTGCAGCCAGACC A G EIF4EBP1 Ensembl:ENSG00000187840 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:38030501..38030767;chr8:38030501..38030669;chr8:38030501..38030662 31548705,26863196 m1A-IP-seq:(High) rs1393205250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1055648,Human_RBP_ID_4984139,Human_RBP_ID_5328818,Human_RBP_ID_9224541,Human_RBP_ID_22465807,Human_RBP_ID_27124406 RMVar_hsa_circ_85790,RMVar_hsa_circ_251330 110071 RMVar_ID_110071 Human_SNP_ID_359701326 m1A Human chr8 + 38030679 38030679 38030679 ACGGCGTGCAGCTCCCGCCCGGGGACTACAGCACGACCCCCGGCGGCACGCTCTTCAGCACCACC ACGGCGTGCAGCTCCCGCCCGGGGACTACAGCTCGACCCCCGGCGGCACGCTCTTCAGCACCACC A T EIF4EBP1 Ensembl:ENSG00000187840 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1311299005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4984143,Human_RBP_ID_8686500,Human_RBP_ID_17672291 Human_Splice_Rec_965905 RMVar_hsa_circ_85790,RMVar_hsa_circ_251330 110072 RMVar_ID_110072 Human_SNP_ID_359709351 m1A Human chr8 + 38064157 38064157 38064157 GAGGTCAGAAAGGAATTGCTGGTTTAGGAATTATGCAGAGTGAACAGCAAGGAGACCAAAGATGG GAGGTCAGAAAGGAATTGCTGGTTTAGGAATTGTGCAGAGTGAACAGCAAGGAGACCAAAGATGG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38063972..38064212 26863196 MeRIP-seq:(Medium) rs757832649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1696323,Human_RBP_ID_16409934,Human_RBP_ID_21614669 110073 RMVar_ID_110073 Human_SNP_ID_359709938 m1A Human chr8 + 38066528 38066528 38066528 GTTGGAGATGTCAGAACAGGCAGTGACAGGTGAGTGTCAAGGTAAAGCAGGTAGAGGAGAGACCT GTTGGAGATGTCAGAACAGGCAGTGACAGGTGGGTGTCAAGGTAAAGCAGGTAGAGGAGAGACCT A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38066486..38066574 26863196 MeRIP-seq:(Medium) rs1447067157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16409991 110074 RMVar_ID_110074 Human_SNP_ID_359720920 m1A Human chr8 + 38105579 38105579 38105579 CGTGATGGCGGCGGCAGGAGCAGGACCTGGCCAGGAAGCGGGTGCCGGGCCTGGCCCAGGAGCGG CGTGATGGCGGCGGCAGGAGCAGGACCTGGCCCGGAAGCGGGTGCCGGGCCTGGCCCAGGAGCGG A C ASH2L Ensembl:ENSG00000129691 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38105526..38105777 26863196 MeRIP-seq:(Medium) rs745453407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995432,Human_RBP_ID_17672374,Human_RBP_ID_18426683,Human_RBP_ID_26359755 110075 RMVar_ID_110075 Human_SNP_ID_359720935 m1A Human chr8 - 38105598 38105598 38105598 GCCCCTGTTGCATTTGCGACCGCTCCTGGGCCAGGCCCGGCACCCGCTTCCTGGCCAGGTCCTGC GCCCCTGTTGCATTTGCGACCGCTCCTGGGCCGGGCCCGGCACCCGCTTCCTGGCCAGGTCCTGC T C RF00017-4487,RF00017-4503,lnc-STAR-1,RF00017-4596,lnc-STAR-1:2,RF00017-4544 RNACentral:URS000095255B,RNACentral:URS0000948B80,RNACentral:URS0000D5CD1B,RNACentral:URS0000934741,RNACentral:URS0000D585D2,RNACentral:URS000093B8FA SRP RNA,SRP RNA,lincRNA,SRP RNA,lincRNA,SRP RNA intron,intron,exon,intron,exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:38105551..38105842 26863196 MeRIP-seq:(Medium) rs758553198 Functional Loss SNV dbSNP153 33..33 33 - - - 110076 RMVar_ID_110076 Human_SNP_ID_359721464 m1A Human chr8 + 38107089 38107089 38107089 CAGGCGGGCTCCGTGGATGAAGAGAATGGCCGACAGTTGGGTGAGGTAGAGCTGCAATGTGGGAT CAGGCGGGCTCCGTGGATGAAGAGAATGGCCGGCAGTTGGGTGAGGTAGAGCTGCAATGTGGGAT A G ASH2L Ensembl:ENSG00000129691 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38107021..38107125 26863196 MeRIP-seq:(Medium) rs746275587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960082,Human_RBP_ID_9224558,Human_RBP_ID_9406200,Human_RBP_ID_16410370,Human_RBP_ID_19021938,Human_RBP_ID_19140102,Human_RBP_ID_21905396,Human_RBP_ID_23088087,Human_RBP_ID_24257009 Human_Splice_Rec_965948,Human_Splice_Rec_965949,Human_Splice_Rec_965956,Human_Splice_Rec_965957,Human_Splice_Rec_966014,Human_Splice_Rec_966015,Human_Splice_Rec_966044,Human_Splice_Rec_966045 Human_miRNA_ID_2012436 RMVar_hsa_circ_25612,RMVar_hsa_circ_110185,RMVar_hsa_circ_354244,RMVar_hsa_circ_38610,RMVar_hsa_circ_251334,RMVar_hsa_circ_251336,RMVar_hsa_circ_291489,RMVar_hsa_circ_374069,RMVar_hsa_circ_251332,RMVar_hsa_circ_324457,RMVar_hsa_circ_287294,RMVar_hsa_circ_251335,RMVar_hsa_circ_251333 110077 RMVar_ID_110077 Human_SNP_ID_359740380 m1A Human chr8 - 38176425 38176425 38176425 AAGCCGGGGCAGAAGTGCTGGTCTCGGTCGGGATTCCGGGCTTGGTCCCACCGAGGCGGCGACTG AAGCCGGGGCAGAAGTGCTGGTCTCGGTCGGGGTTCCGGGCTTGGTCCCACCGAGGCGGCGACTG T C LSM1 Ensembl:ENSG00000175324 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38176376..38176484 26863196 MeRIP-seq:(Medium) rs1275688015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1055681,Human_RBP_ID_1696368,Human_RBP_ID_4994998,Human_RBP_ID_5123759,Human_RBP_ID_5453486,Human_RBP_ID_7877655,Human_RBP_ID_8919468,Human_RBP_ID_16410620,Human_RBP_ID_22517069,Human_RBP_ID_23140851 110078 RMVar_ID_110078 Human_SNP_ID_359740597 m1A Human chr8 + 38176895 38176895 38176895 GGATCCCATGTCGGCCCTGAGGCGCTCGGGCTACGGCCCCAGTGACGGTCCGTCCTACGGCCGCT GGATCCCATGTCGGCCCTGAGGCGCTCGGGCTGCGGCCCCAGTGACGGTCCGTCCTACGGCCGCT A G BAG4 Ensembl:ENSG00000156735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38176849..38176929 26863196 MeRIP-seq:(Medium) rs931803291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995439,Human_RBP_ID_9313380,Human_RBP_ID_27538345 RMVar_hsa_circ_251365,RMVar_hsa_circ_112352 110079 RMVar_ID_110079 Human_SNP_ID_359754588 m1A Human chr8 + 38231840 38231838 38231841 AGTGTCCTCCTCAGGGAGGGCAGGAGAGCCTGAGGAGTGGCGGGGCCGCCAGGTGAGACCGCGTC AGTGTCCTCCTCAGGGAGGGCAGGAGAGCCT___GAGTGGCGGGGCCGCCAGGTGAGACCGCGTC TGAG T DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38231701..38231875 32194978 MeRIP-seq:(Medium) rs1355781397 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4995000 Human_Splice_Rec_966205,Human_Splice_Rec_966239,Human_Splice_Rec_966247,Human_Splice_Rec_966255,Human_Splice_Rec_966261,Human_Splice_Rec_966267,Human_Splice_Rec_966273 110080 RMVar_ID_110080 Human_SNP_ID_359754590 m1A Human chr8 - 38231845 38231845 38231845 CGCCCGACGCGGTCTCACCTGGCGGCCCCGCCACTCCTCAGGCTCTCCTGCCCTCCCTGAGGAGG CGCCCGACGCGGTCTCACCTGGCGGCCCCGCCGCTCCTCAGGCTCTCCTGCCCTCCCTGAGGAGG T C RF00017-4503,RF00017-4596,RF00017-4544 RNACentral:URS0000948B80,RNACentral:URS0000934741,RNACentral:URS000093B8FA SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38231800..38231893 26863196 MeRIP-seq:(Medium) rs1432430427 Functional Loss SNV dbSNP153 33..33 33 - - - 110081 RMVar_ID_110081 Human_SNP_ID_359754592 m1A Human chr8 + 38231858 38231858 38231858 GGCAGGAGAGCCTGAGGAGTGGCGGGGCCGCCAGGTGAGACCGCGTCGGGCGGGCGGCTGGACCG GGCAGGAGAGCCTGAGGAGTGGCGGGGCCGCCCGGTGAGACCGCGTCGGGCGGGCGGCTGGACCG A C DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38231746..38231961 26863196 MeRIP-seq:(Medium) rs1170420591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_844900,Human_RBP_ID_4995000 Human_Splice_Rec_966205,Human_Splice_Rec_966239,Human_Splice_Rec_966247,Human_Splice_Rec_966255,Human_Splice_Rec_966261,Human_Splice_Rec_966267,Human_Splice_Rec_966273 110082 RMVar_ID_110082 Human_SNP_ID_359755272 m1A Human chr8 + 38234513 38234500 38234514 GGGATGAACTGGCATCGGAAGTGAGACGATGTACGTGGTTTTACAAGGGGGACAAAGACAATAAG GGGATGAACTGGCATCGGAA______________GTGGTTTTACAAGGGGGACAAAGACAATAAG AGTGAGACGATGTAC A DDHD2 Ensembl:ENSG00000085788 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:38234463..38238277 32194978 MeRIP-seq:(Medium) rs1554511216 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_699223,Human_RBP_ID_9313383,Human_RBP_ID_9405342,Human_RBP_ID_24257170,Human_RBP_ID_26832674 Human_Splice_Rec_966199,Human_Splice_Rec_966209,Human_Splice_Rec_966243,Human_Splice_Rec_966265,Human_Splice_Rec_966271,Human_Splice_Rec_966277,Human_Splice_Rec_966287,Human_Splice_Rec_966319 RMVar_hsa_circ_19263,RMVar_hsa_circ_127338,RMVar_hsa_circ_357349,RMVar_hsa_circ_367371,RMVar_hsa_circ_343422,RMVar_hsa_circ_64088,RMVar_hsa_circ_251367,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_251366,RMVar_hsa_circ_328935,RMVar_hsa_circ_49606,RMVar_hsa_circ_251368 110083 RMVar_ID_110083 Human_SNP_ID_359761899 m1A Human chr8 - 38261031 38261031 38261031 AGACTTAGCCTTCAGTTCAACACAAACAAGAGATAAGTGTACTCCAAAATGCCTTCTGAATCTCA AGACTTAGCCTTCAGTTCAACACAAACAAGAGGTAAGTGTACTCCAAAATGCCTTCTGAATCTCA T C RF00017-4596,RF00017-4544 RNACentral:URS0000934741,RNACentral:URS000093B8FA SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:38260980..38261081 32194978 MeRIP-seq:(Medium) rs897601870 Functional Loss SNV dbSNP153 33..33 33 - - - 110084 RMVar_ID_110084 Human_SNP_ID_359763006 m1A Human chr8 + 38266296 38266296 38266296 ACTTCCCTGCCAGGTAGAAGGACGCAAAGGCCAGACCAGCAAATGCAACTGGAACAAGAAAAACT ACTTCCCTGCCAGGTAGAAGGACGCAAAGGCCGGACCAGCAAATGCAACTGGAACAAGAAAAACT A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:38266223..38266323 32194978 MeRIP-seq:(Medium) rs1466016736 Functional Loss SNV dbSNP153 33..33 33 - - - 110085 RMVar_ID_110085 Human_SNP_ID_359763862 m1A Human chr8 - 38269162 38269162 38269162 GAAGGCGGCGGCGGCGGTGGCCTTTGGGGCCGAAGTGGGCGTGCGGCTCGCGCTGTTCGCGGCCT GAAGGCGGCGGCGGCGGTGGCCTTTGGGGCCGGAGTGGGCGTGCGGCTCGCGCTGTTCGCGGCCT T C PLPP5 Ensembl:ENSG00000147535 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:38269059..38269166;chr8:38269088..38269186 26863196 MeRIP-seq:(Medium) rs761734170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795685,Human_RBP_ID_4995001,Human_RBP_ID_18426685,Human_RBP_ID_19140107,Human_RBP_ID_23120769 Human_Splice_Rec_966439,Human_Splice_Rec_966457,Human_Splice_Rec_966469,Human_Splice_Rec_966481,Human_Splice_Rec_966493,Human_Splice_Rec_966505,Human_Splice_Rec_966519,Human_Splice_Rec_966527 RMVar_hsa_circ_124664,RMVar_hsa_circ_251398 110086 RMVar_ID_110086 Human_SNP_ID_359788969 m1A Human chr8 - 38381036 38381036 38381036 TTCTGTGTCTTTCTTTCAAGGCTAGAGAATAGAGAAGCTGGTGGTTATGGGATTGTGATTGTTGT TTCTGTGTCTTTCTTTCAAGGCTAGAGAATAGGGAAGCTGGTGGTTATGGGATTGTGATTGTTGT T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38381028..38381322 26863196 MeRIP-seq:(Medium) rs975814568 Functional Loss SNV dbSNP153 33..33 33 - - - 110087 RMVar_ID_110087 Human_SNP_ID_359789345 m1A Human chr8 - 38382226 38382226 38382226 CGGCGGCGGCGGGAGAGGCGGCGGCGGCGGCCAGCACGGAGGCGGAGGCCGAGGGGGCTGTGCAC CGGCGGCGGCGGGAGAGGCGGCGGCGGCGGCCGGCACGGAGGCGGAGGCCGAGGGGGCTGTGCAC T C NSD3 Ensembl:ENSG00000147548 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:38381656..38382272;chr8:38381861..38382296;chr8:38381822..38382295 26863196 MeRIP-seq:(Medium) rs1182450702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995005,Human_RBP_ID_8222295 110088 RMVar_ID_110088 Human_SNP_ID_359792297 m1A Human chr8 - 38393609 38393608 38393610 TTGAGATGGCATCTCACTCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCGCTGCAACCTCCGC TTGAGATGGCATCTCACTCCAGGCTGGAGTG__GTGGCACGATCTCGGCTCGCTGCAACCTCCGC CTG C lnc-NSD3-8 RNACentral:URS00008BE38E lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38393533..38393635 32194978 MeRIP-seq:(Medium) rs1424275286 Functional Loss DEL dbSNP153 32..33 33 - - - 110089 RMVar_ID_110089 Human_SNP_ID_359797364 m1A Human chr8 + 38413534 38413534 38413534 CCTGGTAGGCAGCCGGCTCCTGCCAGCAGGAAAGGGGACAGGGACGGACAGGTGGTGGGCCCAGC CCTGGTAGGCAGCCGGCTCCTGCCAGCAGGAAGGGGGACAGGGACGGACAGGTGGTGGGCCCAGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:38413486..38413587 32194978 MeRIP-seq:(Medium) rs1414051259 Functional Loss SNV dbSNP153 33..33 33 - - - 110090 RMVar_ID_110090 Human_SNP_ID_359797648 m1A Human chr8 + 38414211 38414211 38414211 TCCATGCGGTGACCCTCCTTCAGCAGCTTGAAAAGTTCCTCCACAGGCACACCGGGGTATGGGGA TCCATGCGGTGACCCTCCTTCAGCAGCTTGAACAGTTCCTCCACAGGCACACCGGGGTATGGGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38414151..38414785 32194978 MeRIP-seq:(Medium) rs780575123 Functional Loss SNV dbSNP153 33..33 33 - - - 110091 RMVar_ID_110091 Human_SNP_ID_359798248 m1A Human chr8 - 38416027 38416027 38416027 TCCCTTGTATGTCATCGTGGAGTATGCCTCCAAGGGCAACCTGCGGGAGTACCTGCAGGCCCGGA TCCCTTGTATGTCATCGTGGAGTATGCCTCCAGGGGCAACCTGCGGGAGTACCTGCAGGCCCGGA T C FGFR1 Ensembl:ENSG00000077782 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38415976..38416075 32194978 MeRIP-seq:(Medium) rs531903077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5534503,Human_RBP_ID_9405350,Human_RBP_ID_19021951 Human_Splice_Rec_966896,Human_Splice_Rec_966936,Human_Splice_Rec_966968,Human_Splice_Rec_966996,Human_Splice_Rec_967028,Human_Splice_Rec_967060,Human_Splice_Rec_967094,Human_Splice_Rec_967128,Human_Splice_Rec_967160,Human_Splice_Rec_967194,Human_Splice_Rec_967224,Human_Splice_Rec_967260,Human_Splice_Rec_967290,Human_Splice_Rec_967314,Human_Splice_Rec_967346,Human_Splice_Rec_967374,Human_Splice_Rec_967416,Human_Splice_Rec_967428,Human_Splice_Rec_967440,Human_Splice_Rec_967462 Human_miRNA_ID_2615156,Human_miRNA_ID_2615157,Human_miRNA_ID_2615158 RMVar_hsa_circ_1086,RMVar_hsa_circ_84323,RMVar_hsa_circ_369926,RMVar_hsa_circ_104175,RMVar_hsa_circ_100431,RMVar_hsa_circ_251424,RMVar_hsa_circ_77152,RMVar_hsa_circ_251426,RMVar_hsa_circ_251427,RMVar_hsa_circ_251425,RMVar_hsa_circ_251423,RMVar_hsa_circ_99803,RMVar_hsa_circ_251430 110092 RMVar_ID_110092 Human_SNP_ID_359800627 m1A Human chr8 + 38424145 38424145 38424145 TTGCCAGAAAGATCGTACGTAACTCAGGACACAGGGCTAAGACTGGGAAACGCTTGGTGGAAAGG TTGCCAGAAAGATCGTACGTAACTCAGGACACGGGGCTAAGACTGGGAAACGCTTGGTGGAAAGG A G AC087623.1 Ensembl:ENSG00000255201 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38424144..38424295 32194978 MeRIP-seq:(Medium) rs1057257985 Functional Loss SNV dbSNP153 33..33 33 - - - 110093 RMVar_ID_110093 Human_SNP_ID_359812551 m1A Human chr8 + 38467804 38467804 38467804 GACGCGGACGGAGGGAAGGGAGGGGAGACCCAAGGGGCGCGGATCGCCCGGGAGGGAGCCAGGAG GACGCGGACGGAGGGAAGGGAGGGGAGACCCACGGGGCGCGGATCGCCCGGGAGGGAGCCAGGAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38467803..38468584 32194978 MeRIP-seq:(Medium) rs1303569424 Functional Loss SNV dbSNP153 33..33 33 - - - 110094 RMVar_ID_110094 Human_SNP_ID_359812552 m1A Human chr8 + 38467804 38467804 38467804 GACGCGGACGGAGGGAAGGGAGGGGAGACCCAAGGGGCGCGGATCGCCCGGGAGGGAGCCAGGAG GACGCGGACGGAGGGAAGGGAGGGGAGACCCAGGGGGCGCGGATCGCCCGGGAGGGAGCCAGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38467803..38468584 32194978 MeRIP-seq:(Medium) rs1303569424 Functional Loss SNV dbSNP153 33..33 33 - - - 110095 RMVar_ID_110095 Human_SNP_ID_359812824 m1A Human chr8 - 38468486 38468486 38468486 GGGAGCTGGGCGGCCACGTCCGGACGGGACCGAGACCCCTCGTAGCGCATTGCGGCGACCTCGCC GGGAGCTGGGCGGCCACGTCCGGACGGGACCGGGACCCCTCGTAGCGCATTGCGGCGACCTCGCC T C FGFR1 Ensembl:ENSG00000077782 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1007064310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_699495,Human_RBP_ID_4995014,Human_RBP_ID_9405364 110096 RMVar_ID_110096 Human_SNP_ID_359812834 m1A Human chr8 + 38468500 38468500 38468500 AATGCGCTACGAGGGGTCTCGGTCCCGTCCGGACGTGGCCGCCCAGCTCCCGGCACACCCGGGTT AATGCGCTACGAGGGGTCTCGGTCCCGTCCGGCCGTGGCCGCCCAGCTCCCGGCACACCCGGGTT A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:38468401..38468580 26863410 MeRIP-seq:(Medium) rs994250673 Functional Loss SNV dbSNP153 33..33 33 - - - 110097 RMVar_ID_110097 Human_SNP_ID_359812835 m1A Human chr8 + 38468500 38468500 38468500 AATGCGCTACGAGGGGTCTCGGTCCCGTCCGGACGTGGCCGCCCAGCTCCCGGCACACCCGGGTT AATGCGCTACGAGGGGTCTCGGTCCCGTCCGGGCGTGGCCGCCCAGCTCCCGGCACACCCGGGTT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:38468401..38468580 26863410 MeRIP-seq:(Medium) rs994250673 Functional Loss SNV dbSNP153 33..33 33 - - - 110098 RMVar_ID_110098 Human_SNP_ID_359887788 m1A Human chr8 + 38769620 38769620 38769620 ATGTATATGTATGTGAGGCTGTATGGGTCAGGAATGTGGTGTGTGTGACTACGTGGGGTGTGTGT ATGTATATGTATGTGAGGCTGTATGGGTCAGGGATGTGGTGTGTGTGACTACGTGGGGTGTGTGT A G TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38768773..38770071 26863196 MeRIP-seq:(Medium) rs1452717258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8222309 RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_61214 110099 RMVar_ID_110099 Human_SNP_ID_359892020 m1A Human chr8 + 38787264 38787264 38787264 GCGGGAGTCCGCGAGCCGGGAGCGGGAGCAGCAGAGGTCTAGCAGCCGGGCGCCGCGGGCCGGGG GCGGGAGTCCGCGAGCCGGGAGCGGGAGCAGCTGAGGTCTAGCAGCCGGGCGCCGCGGGCCGGGG A T TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:38787226..38787525 26863196 MeRIP-seq:(Medium) rs1283336564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_845174,Human_RBP_ID_4995441,Human_RBP_ID_22367512,Human_RBP_ID_22732647 RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_29816,RMVar_hsa_circ_61214 110100 RMVar_ID_110100 Human_SNP_ID_359892110 m1A Human chr8 + 38787477 38787477 38787477 ACTCGTTTAACCACATCCGCGCCTCTGCTGGAAACGCTTGCTGGCGCCTGTCACCGGTTCCCTCC ACTCGTTTAACCACATCCGCGCCTCTGCTGGAGACGCTTGCTGGCGCCTGTCACCGGTTCCCTCC A G TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38787426..38787525 32194978 MeRIP-seq:(Medium) rs1468103497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_29816,RMVar_hsa_circ_61214 110101 RMVar_ID_110101 Human_SNP_ID_359892218 m1A Human chr8 + 38787736 38787736 38787736 AGGAGGATTCGCAAGCCGAGACCAAATCCTTGAGTTTCAGGCAAGTACACGGCGTCCCCGCTGAG AGGAGGATTCGCAAGCCGAGACCAAATCCTTGGGTTTCAGGCAAGTACACGGCGTCCCCGCTGAG A G TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38787576..38787750 32194978 MeRIP-seq:(Medium) rs1170365211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9313794,Human_RBP_ID_19140123,Human_RBP_ID_23087940 RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_29816,RMVar_hsa_circ_61214 110102 RMVar_ID_110102 Human_SNP_ID_359920003 m1A Human chr8 - 38901361 38901361 38901361 CGCCCCTCCGGCCGCCGGGTCCGCCGCGCTCCAGGGATTTCTGGGTCTGCCTGCCAAACTCTCCG CGCCCCTCCGGCCGCCGGGTCCGCCGCGCTCCGGGGATTTCTGGGTCTGCCTGCCAAACTCTCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:38901326..38901479 26863196 MeRIP-seq:(Medium) rs527726152 Functional Loss SNV dbSNP153 33..33 33 - - - 110103 RMVar_ID_110103 Human_SNP_ID_359923944 m1A Human chr8 + 38917957 38917957 38917957 CAGGAATGCCTTATGTGGATCGGCAGAACCGAATCTGTGGGTTTCTGGACATCGAGGAGCATGAG CAGGAATGCCTTATGTGGATCGGCAGAACCGAGTCTGTGGGTTTCTGGACATCGAGGAGCATGAG A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38917865..38917987 26863196 MeRIP-seq:(Medium) rs1431924162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_959069,Human_RBP_ID_1055752,Human_RBP_ID_4995445,Human_RBP_ID_5629065,Human_RBP_ID_9406231,Human_RBP_ID_24257813,Human_RBP_ID_27831264 Human_Splice_Rec_967990,Human_Splice_Rec_968034,Human_Splice_Rec_968056 RMVar_hsa_circ_35066,RMVar_hsa_circ_340526,RMVar_hsa_circ_362075,RMVar_hsa_circ_372201,RMVar_hsa_circ_73785,RMVar_hsa_circ_251452 110104 RMVar_ID_110104 Human_SNP_ID_359923945 m1A Human chr8 - 38917960 38917959 38917961 GTTCTCATGCTCCTCGATGTCCAGAAACCCACAGATTCGGTTCTGCCGATCCACATAAGGCATTC GTTCTCATGCTCCTCGATGTCCAGAAACCCA__GATTCGGTTCTGCCGATCCACATAAGGCATTC CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38917847..38917980 26863196 MeRIP-seq:(Medium) rs940962664 Functional Loss DEL dbSNP153 32..33 33 - - - 110105 RMVar_ID_110105 Human_SNP_ID_359923947 m1A Human chr8 - 38917960 38917960 38917960 GTTCTCATGCTCCTCGATGTCCAGAAACCCACAGATTCGGTTCTGCCGATCCACATAAGGCATTC GTTCTCATGCTCCTCGATGTCCAGAAACCCACGGATTCGGTTCTGCCGATCCACATAAGGCATTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38917847..38917980 26863196 MeRIP-seq:(Medium) rs757953837 Functional Loss SNV dbSNP153 33..33 33 - - - 110106 RMVar_ID_110106 Human_SNP_ID_359926479 m1A Human chr8 - 38927832 38927830 38927832 TCCCCATCCATCCCGATGTCCTGGCCAGAACAAACTTTCTTAACAGATAACATCTGTAGCACTTT TCCCCATCCATCCCGATGTCCTGGCCAGAACA__CTTTCTTAACAGATAACATCTGTAGCACTTT GTT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:38927829..38928024 26863196 MeRIP-seq:(Medium) rs112797658 Functional Loss DEL dbSNP153 33..34 33 - - - 110107 RMVar_ID_110107 Human_SNP_ID_359937723 m1A Human chr8 + 38972530 38972530 38972530 TGTAGTTCAATATGAGATAAATTATTATCTTCAATGAAACAAGCTCTAAAAGCATTCCATTCCTA TGTAGTTCAATATGAGATAAATTATTATCTTCGATGAAACAAGCTCTAAAAGCATTCCATTCCTA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7001984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 110108 RMVar_ID_110108 Human_SNP_ID_359937724 m1A Human chr8 + 38972530 38972530 38972531 TGTAGTTCAATATGAGATAAATTATTATCTTCAATGAAACAAGCTCTAAAAGCATTCCATTCCTA TGTAGTTCAATATGAGATAAATTATTATCTTCGGTGAAACAAGCTCTAAAAGCATTCCATTCCTA AA GG PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs386724605 Functional Loss MNV dbSNP153 33..34 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 110109 RMVar_ID_110109 Human_SNP_ID_359944244 m1A Human chr8 + 38996455 38996455 38996455 CAACCACCTAGCACCATCTTCCCGGGCACAGGAGCGGAGACCCGGCCTCAACCACAACCCCAGGC CAACCACCTAGCACCATCTTCCCGGGCACAGGGGCGGAGACCCGGCCTCAACCACAACCCCAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38996406..38996480 26863196 MeRIP-seq:(Medium) rs1460945668 Functional Loss SNV dbSNP153 33..33 33 - - - 110110 RMVar_ID_110110 Human_SNP_ID_359944539 m1A Human chr8 + 38997023 38997023 38997023 GGGTTGGAAAATGATGGAAGAGGCGGAGGTGGAGGCGACCGAGTGCTGAGAGGAACCTGCGGAAT GGGTTGGAAAATGATGGAAGAGGCGGAGGTGGCGGCGACCGAGTGCTGAGAGGAACCTGCGGAAT A C ADAM9 Ensembl:ENSG00000168615 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:38996976..38997125 26863196 MeRIP-seq:(Medium) rs376934408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795963,Human_RBP_ID_845395,Human_RBP_ID_960662,Human_RBP_ID_4985208,Human_RBP_ID_8686821,Human_RBP_ID_18427063,Human_RBP_ID_26359775,Human_RBP_ID_27831265 RMVar_hsa_circ_78597,RMVar_hsa_circ_106995,RMVar_hsa_circ_251469,RMVar_hsa_circ_251470 110111 RMVar_ID_110111 Human_SNP_ID_359944546 m1A Human chr8 + 38997028 38997028 38997028 GGAAAATGATGGAAGAGGCGGAGGTGGAGGCGACCGAGTGCTGAGAGGAACCTGCGGAATCGGCC GGAAAATGATGGAAGAGGCGGAGGTGGAGGCGTCCGAGTGCTGAGAGGAACCTGCGGAATCGGCC A T ADAM9 Ensembl:ENSG00000168615 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38996883..38997175 26863196 MeRIP-seq:(Medium) rs1345649452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795963,Human_RBP_ID_845395,Human_RBP_ID_960662,Human_RBP_ID_4985208,Human_RBP_ID_8686821,Human_RBP_ID_18427063,Human_RBP_ID_26359775,Human_RBP_ID_27831265 RMVar_hsa_circ_78597,RMVar_hsa_circ_106995,RMVar_hsa_circ_251469,RMVar_hsa_circ_251470 110112 RMVar_ID_110112 Human_SNP_ID_359944549 m1A Human chr8 + 38997032 38997032 38997032 AATGATGGAAGAGGCGGAGGTGGAGGCGACCGAGTGCTGAGAGGAACCTGCGGAATCGGCCGAGA AATGATGGAAGAGGCGGAGGTGGAGGCGACCGGGTGCTGAGAGGAACCTGCGGAATCGGCCGAGA A G ADAM9 Ensembl:ENSG00000168615 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38996884..38997211 26863196 MeRIP-seq:(Medium) rs1300969377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795963,Human_RBP_ID_845395,Human_RBP_ID_960662,Human_RBP_ID_4985208,Human_RBP_ID_8686821,Human_RBP_ID_26359775,Human_RBP_ID_27831265 RMVar_hsa_circ_78597,RMVar_hsa_circ_106995,RMVar_hsa_circ_251469,RMVar_hsa_circ_251470 110113 RMVar_ID_110113 Human_SNP_ID_359947263 m1A Human chr8 + 39007840 39007840 39007840 TTTTGATTTTTCATTATATTGTGTTCCCACGTAGTTTTTCAGTTTCACTTATTATATTTGTTTTT TTTTGATTTTTCATTATATTGTGTTCCCACGTGGTTTTTCAGTTTCACTTATTATATTTGTTTTT A G ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:39007836..39007920 26863196 MeRIP-seq:(Medium) rs781660406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78597,RMVar_hsa_circ_106995,RMVar_hsa_circ_251469,RMVar_hsa_circ_251470,RMVar_hsa_circ_251471 110114 RMVar_ID_110114 Human_SNP_ID_359947264 m1A Human chr8 + 39007840 39007840 39007840 TTTTGATTTTTCATTATATTGTGTTCCCACGTAGTTTTTCAGTTTCACTTATTATATTTGTTTTT TTTTGATTTTTCATTATATTGTGTTCCCACGTTGTTTTTCAGTTTCACTTATTATATTTGTTTTT A T ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:39007836..39007920 26863196 MeRIP-seq:(Medium) rs781660406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78597,RMVar_hsa_circ_106995,RMVar_hsa_circ_251469,RMVar_hsa_circ_251470,RMVar_hsa_circ_251471 110115 RMVar_ID_110115 Human_SNP_ID_359951291 m1A Human chr8 + 39023277 39023277 39023277 TGATGTGCTGGGGAACTTCGTGCAGTGGCGGGAAAAGTTTCTTATCACACGTCGGAGACATGACA TGATGTGCTGGGGAACTTCGTGCAGTGGCGGGGAAAGTTTCTTATCACACGTCGGAGACATGACA A G ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:39023226..39026758 32194978 MeRIP-seq:(Medium) rs79918741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021965,Human_RBP_ID_23087861,Human_RBP_ID_27831269 Human_Splice_Rec_968169,Human_Splice_Rec_968215,Human_Splice_Rec_968253,Human_Splice_Rec_968291 RMVar_hsa_circ_78597,RMVar_hsa_circ_251474,RMVar_hsa_circ_251470,RMVar_hsa_circ_337055,RMVar_hsa_circ_284404,RMVar_hsa_circ_251473,RMVar_hsa_circ_92395,RMVar_hsa_circ_63561,RMVar_hsa_circ_7538,RMVar_hsa_circ_41264,RMVar_hsa_circ_63680,RMVar_hsa_circ_356194,RMVar_hsa_circ_251475,RMVar_hsa_circ_116755,RMVar_hsa_circ_375758,RMVar_hsa_circ_251476,RMVar_hsa_circ_51351,RMVar_hsa_circ_42324,RMVar_hsa_circ_48076,RMVar_hsa_circ_251477,RMVar_hsa_circ_25409,RMVar_hsa_circ_62824,RMVar_hsa_circ_312963,RMVar_hsa_circ_340527,RMVar_hsa_circ_360126,RMVar_hsa_circ_305368,RMVar_hsa_circ_29095,RMVar_hsa_circ_61752,RMVar_hsa_circ_32240,RMVar_hsa_circ_251478 110116 RMVar_ID_110116 Human_SNP_ID_359951292 m1A Human chr8 + 39023277 39023277 39023277 TGATGTGCTGGGGAACTTCGTGCAGTGGCGGGAAAAGTTTCTTATCACACGTCGGAGACATGACA TGATGTGCTGGGGAACTTCGTGCAGTGGCGGGTAAAGTTTCTTATCACACGTCGGAGACATGACA A T ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:39023226..39026758 32194978 MeRIP-seq:(Medium) rs79918741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021965,Human_RBP_ID_23087861,Human_RBP_ID_27831269 Human_Splice_Rec_968169,Human_Splice_Rec_968215,Human_Splice_Rec_968253,Human_Splice_Rec_968291 RMVar_hsa_circ_78597,RMVar_hsa_circ_251474,RMVar_hsa_circ_251470,RMVar_hsa_circ_337055,RMVar_hsa_circ_284404,RMVar_hsa_circ_251473,RMVar_hsa_circ_92395,RMVar_hsa_circ_63561,RMVar_hsa_circ_7538,RMVar_hsa_circ_41264,RMVar_hsa_circ_63680,RMVar_hsa_circ_356194,RMVar_hsa_circ_251475,RMVar_hsa_circ_116755,RMVar_hsa_circ_375758,RMVar_hsa_circ_251476,RMVar_hsa_circ_51351,RMVar_hsa_circ_42324,RMVar_hsa_circ_48076,RMVar_hsa_circ_251477,RMVar_hsa_circ_25409,RMVar_hsa_circ_62824,RMVar_hsa_circ_312963,RMVar_hsa_circ_340527,RMVar_hsa_circ_360126,RMVar_hsa_circ_305368,RMVar_hsa_circ_29095,RMVar_hsa_circ_61752,RMVar_hsa_circ_32240,RMVar_hsa_circ_251478 110117 RMVar_ID_110117 Human_SNP_ID_359951299 m1A Human chr8 + 39023291 39023291 39023291 ACTTCGTGCAGTGGCGGGAAAAGTTTCTTATCACACGTCGGAGACATGACAGTGCACAGCTAGTT ACTTCGTGCAGTGGCGGGAAAAGTTTCTTATCGCACGTCGGAGACATGACAGTGCACAGCTAGTT A G ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:39023242..39023355 26863196 MeRIP-seq:(Medium) rs1266058904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_88974,Human_RBP_ID_19021966,Human_RBP_ID_23087861,Human_RBP_ID_27831269 Human_Splice_Rec_968169,Human_Splice_Rec_968215,Human_Splice_Rec_968253,Human_Splice_Rec_968291 RMVar_hsa_circ_78597,RMVar_hsa_circ_251474,RMVar_hsa_circ_251470,RMVar_hsa_circ_337055,RMVar_hsa_circ_284404,RMVar_hsa_circ_251473,RMVar_hsa_circ_92395,RMVar_hsa_circ_63561,RMVar_hsa_circ_7538,RMVar_hsa_circ_41264,RMVar_hsa_circ_63680,RMVar_hsa_circ_356194,RMVar_hsa_circ_251475,RMVar_hsa_circ_116755,RMVar_hsa_circ_375758,RMVar_hsa_circ_251476,RMVar_hsa_circ_51351,RMVar_hsa_circ_42324,RMVar_hsa_circ_48076,RMVar_hsa_circ_251477,RMVar_hsa_circ_25409,RMVar_hsa_circ_62824,RMVar_hsa_circ_312963,RMVar_hsa_circ_340527,RMVar_hsa_circ_360126,RMVar_hsa_circ_305368,RMVar_hsa_circ_29095,RMVar_hsa_circ_61752,RMVar_hsa_circ_32240,RMVar_hsa_circ_251478 110118 RMVar_ID_110118 Human_SNP_ID_359959928 m1A Human chr8 - 39054490 39054490 39054490 CTTACAGGTACTTCCTTCGCAGCAAGGGTCCAATTCACATTCCTGTGAACATAAAATGACTGTCA CTTACAGGTACTTCCTTCGCAGCAAGGGTCCAGTTCACATTCCTGTGAACATAAAATGACTGTCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:39054476..39054525 32194978 MeRIP-seq:(Medium) rs760187937 Functional Loss SNV dbSNP153 33..33 33 - - - 110119 RMVar_ID_110119 Human_SNP_ID_359960266 m1A Human chr8 + 39055756 39055756 39055756 GGCATGTGCCAGTATTATGATGCTCAATGTCAAGTCATCTTTGGCTCAAGTAAGATATCATCATT GGCATGTGCCAGTATTATGATGCTCAATGTCACGTCATCTTTGGCTCAAGTAAGATATCATCATT A C ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:39055706..39071331 32194978 MeRIP-seq:(Medium) rs1481801039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18896431 Human_Splice_Rec_968179,Human_Splice_Rec_968225,Human_Splice_Rec_968263,Human_Splice_Rec_968301 RMVar_hsa_circ_78597,RMVar_hsa_circ_251474,RMVar_hsa_circ_251470,RMVar_hsa_circ_337055,RMVar_hsa_circ_19904,RMVar_hsa_circ_63561,RMVar_hsa_circ_7538,RMVar_hsa_circ_116755,RMVar_hsa_circ_251476,RMVar_hsa_circ_51351,RMVar_hsa_circ_25409,RMVar_hsa_circ_340527,RMVar_hsa_circ_90549,RMVar_hsa_circ_61752,RMVar_hsa_circ_94910,RMVar_hsa_circ_251480,RMVar_hsa_circ_251481,RMVar_hsa_circ_324282,RMVar_hsa_circ_354983,RMVar_hsa_circ_93563,RMVar_hsa_circ_33456,RMVar_hsa_circ_251488,RMVar_hsa_circ_306791,RMVar_hsa_circ_251484,RMVar_hsa_circ_16207,RMVar_hsa_circ_251483,RMVar_hsa_circ_323656,RMVar_hsa_circ_281303,RMVar_hsa_circ_287498,RMVar_hsa_circ_270010,RMVar_hsa_circ_251486,RMVar_hsa_circ_251487,RMVar_hsa_circ_251485 110120 RMVar_ID_110120 Human_SNP_ID_359971147 m1A Human chr8 + 39101918 39101917 39101918 AGTACCAACCTATGCAGCCAAGCAACCTCAGCAGTTCCCATCAAGGTCAGAAGAAAATTTGCTTA AGTACCAACCTATGCAGCCAAGCAACCTCAGC_GTTCCCATCAAGGTCAGAAGAAAATTTGCTTA CA C ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:39101824..39101972 26863196 MeRIP-seq:(Medium) rs781556720 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_960680,Human_RBP_ID_17320006,Human_RBP_ID_17547307,Human_RBP_ID_17666110 Human_Splice_Rec_968190,Human_Splice_Rec_968191,Human_Splice_Rec_968234,Human_Splice_Rec_968235,Human_Splice_Rec_968272,Human_Splice_Rec_968273,Human_Splice_Rec_968312,Human_Splice_Rec_968313,Human_Splice_Rec_968326,Human_Splice_Rec_968327 RMVar_hsa_circ_116755,RMVar_hsa_circ_251476,RMVar_hsa_circ_94910,RMVar_hsa_circ_251481,RMVar_hsa_circ_107886,RMVar_hsa_circ_251489,RMVar_hsa_circ_48481 110121 RMVar_ID_110121 Human_SNP_ID_359971149 m1A Human chr8 + 39101918 39101918 39101918 AGTACCAACCTATGCAGCCAAGCAACCTCAGCAGTTCCCATCAAGGTCAGAAGAAAATTTGCTTA AGTACCAACCTATGCAGCCAAGCAACCTCAGCGGTTCCCATCAAGGTCAGAAGAAAATTTGCTTA A G ADAM9 Ensembl:ENSG00000168615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:39101824..39101972 26863196 MeRIP-seq:(Medium) rs1169183064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960680,Human_RBP_ID_17320006,Human_RBP_ID_17547307,Human_RBP_ID_17666110 Human_Splice_Rec_968190,Human_Splice_Rec_968191,Human_Splice_Rec_968234,Human_Splice_Rec_968235,Human_Splice_Rec_968272,Human_Splice_Rec_968273,Human_Splice_Rec_968312,Human_Splice_Rec_968313,Human_Splice_Rec_968326,Human_Splice_Rec_968327 RMVar_hsa_circ_116755,RMVar_hsa_circ_251476,RMVar_hsa_circ_94910,RMVar_hsa_circ_251481,RMVar_hsa_circ_107886,RMVar_hsa_circ_251489,RMVar_hsa_circ_48481 110122 RMVar_ID_110122 Human_SNP_ID_359971581 m1A Human chr8 - 39103762 39103762 39103762 TTGCAACAGAAAGGCTTTTCAAGAAAACATCAAGAAAAAAAAAAAGTATTAGCTCAGTTCCCTGA TTGCAACAGAAAGGCTTTTCAAGAAAACATCAGGAAAAAAAAAAAGTATTAGCTCAGTTCCCTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:39090076..39103851 32194978 MeRIP-seq:(Medium) rs760415935 Functional Loss SNV dbSNP153 33..33 33 - - - 110123 RMVar_ID_110123 Human_SNP_ID_359971893 m1A Human chr8 - 39104745 39104745 39104745 TAGATACCACAGTAACTTTTTTGTAGGTATTTAAGAAAACCATTTCTTCCTTCTTTCTCCAGCCT TAGATACCACAGTAACTTTTTTGTAGGTATTTTAGAAAACCATTTCTTCCTTCTTTCTCCAGCCT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:39104695..39104796 32194978 MeRIP-seq:(Medium) rs1189435822 Functional Loss SNV dbSNP153 33..33 33 - - - 110124 RMVar_ID_110124 Human_SNP_ID_360583935 m1A Human chr8 - 41490619 41490619 41490619 CCCCACAACCCGGTTCGGCCCGGGAAACACAAACCCGCCTCCTCTGCCCTCCAGCTGCTGTCGCA CCCCACAACCCGGTTCGGCCCGGGAAACACAACCCCGCCTCCTCTGCCCTCCAGCTGCTGTCGCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:41490487..41490940;chr8:41490498..41490748 26863196 MeRIP-seq:(Medium) rs917067896 Functional Loss SNV dbSNP153 33..33 33 - - - 110125 RMVar_ID_110125 Human_SNP_ID_360596034 m1A Human chr8 + 41542128 41542128 41542128 ATAAACAGCCAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG ATAAACAGCCAGGCATGGTGACTCAAGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG A T GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs748130894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2086094,Human_miRNA_ID_2845718,Human_miRNA_ID_2848738 RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 110126 RMVar_ID_110126 Human_SNP_ID_360596555 m1A Human chr8 + 41543968 41543968 41543968 ACCCCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACTGCGC ACCCCAGGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGAATTATAGGCGTGAGCCACTGCGC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1424195388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 110127 RMVar_ID_110127 Human_SNP_ID_360596557 m1A Human chr8 + 41543977 41543976 41543977 GATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACTGCGCACGGCCTGG GATCCACCCACCTCGGCCTCCCAAAGTGCTGG_ATTATAGGCGTGAGCCACTGCGCACGGCCTGG GA G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1188084666 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 110128 RMVar_ID_110128 Human_SNP_ID_360605395 m1A Human chr8 + 41578266 41578266 41578266 GGGAGCGGTCGCCGCGGGATTTGGAGCTGCCTAGCCTCGCGGTCGGTGAGTAGGAGGGAGCTGGC GGGAGCGGTCGCCGCGGGATTTGGAGCTGCCTCGCCTCGCGGTCGGTGAGTAGGAGGGAGCTGGC A C GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:41578218..41578326 26863196 MeRIP-seq:(Medium) rs1381971243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254930,Human_RBP_ID_795261,Human_RBP_ID_846026,Human_RBP_ID_4995025,Human_RBP_ID_18426688,Human_RBP_ID_18452578 Human_Splice_Rec_969875,Human_Splice_Rec_969879,Human_Splice_Rec_969903 RMVar_hsa_circ_85160,RMVar_hsa_circ_251527 110129 RMVar_ID_110129 Human_SNP_ID_360605401 m1A Human chr8 - 41578276 41578276 41578276 GAGGTAAGGGGCCAGCTCCCTCCTACTCACCGACCGCGAGGCTAGGCAGCTCCAAATCCCGCGGC GAGGTAAGGGGCCAGCTCCCTCCTACTCACCGCCCGCGAGGCTAGGCAGCTCCAAATCCCGCGGC T G AC009630.1 Ensembl:ENSG00000253133 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:41578240..41578343 26863196 MeRIP-seq:(Medium) rs999188 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15331,GWAS_ID_15332,GWAS_ID_15333,GWAS_ID_15334,GWAS_ID_15335,GWAS_ID_15336,GWAS_ID_15337,GWAS_ID_15338,GWAS_ID_15339,GWAS_ID_15340,GWAS_ID_15341,GWAS_ID_15342,GWAS_ID_15343,GWAS_ID_15344,GWAS_ID_15345,GWAS_ID_15346,GWAS_ID_15347,GWAS_ID_15348,GWAS_ID_15349,GWAS_ID_15350,GWAS_ID_15351,GWAS_ID_15352,GWAS_ID_15353,GWAS_ID_15354,GWAS_ID_15355,GWAS_ID_15356,GWAS_ID_15357,GWAS_ID_15358,GWAS_ID_15359,GWAS_ID_15360,GWAS_ID_15361,GWAS_ID_15362,GWAS_ID_15363 110130 RMVar_ID_110130 Human_SNP_ID_360612473 m1A Human chr8 + 41604649 41604649 41604649 AGCCTGGATGTAAAGGAGAAAGATGAGAACAAATGATGTGAAAGGAGTTGATCAGGTCACGTTAG AGCCTGGATGTAAAGGAGAAAGATGAGAACAAGTGATGTGAAAGGAGTTGATCAGGTCACGTTAG A G GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:41604642..41604767 26863196 MeRIP-seq:(Medium) rs530067310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16415025 RMVar_hsa_circ_100650,RMVar_hsa_circ_120020,RMVar_hsa_circ_251528,RMVar_hsa_circ_251529 110131 RMVar_ID_110131 Human_SNP_ID_360696487 m1A Human chr8 - 41933198 41933186 41933198 CCACAACCACAACCAGCACCACAGCCTCCACCACCCCAGCAGCAGCCGCAACAGCAGCCGCAGCC CCACAACCACAACCAGCACCACAGCCTCCACC____________GCCGCAACAGCAGCCGCAGCC CTGCTGCTGGGGT C KAT6A Ensembl:ENSG00000083168 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:41933147..41933293 26863196 MeRIP-seq:(Medium) rs1332127484 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_89647,Human_RBP_ID_17320012 RMVar_hsa_circ_264802 110132 RMVar_ID_110132 Human_SNP_ID_360696493 m1A Human chr8 - 41933198 41933198 41933198 CCACAACCACAACCAGCACCACAGCCTCCACCACCCCAGCAGCAGCCGCAACAGCAGCCGCAGCC CCACAACCACAACCAGCACCACAGCCTCCACCCCCCCAGCAGCAGCCGCAACAGCAGCCGCAGCC T G KAT6A Ensembl:ENSG00000083168 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:41933147..41933293 26863196 MeRIP-seq:(Medium) rs754089857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_89647,Human_RBP_ID_17320012 RMVar_hsa_circ_264802 110133 RMVar_ID_110133 Human_SNP_ID_360696957 m1A Human chr8 - 41934360 41934360 41934360 GCCCCGTGTCTCAGAGGAGCAGAGGCAGTCAGAGGAGGAGCAGCAGGAATTAGAGGAGCCAGAGC GCCCCGTGTCTCAGAGGAGCAGAGGCAGTCAGTGGAGGAGCAGCAGGAATTAGAGGAGCCAGAGC T A KAT6A Ensembl:ENSG00000083168 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:41934056..41934600 26863196 MeRIP-seq:(Medium) rs771209341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15082,Human_RBP_ID_5534150 RMVar_hsa_circ_264802,RMVar_hsa_circ_251555 110134 RMVar_ID_110134 Human_SNP_ID_360721764 m1A Human chr8 - 42033665 42033665 42033665 GTGCTCTGATGAAGTAAAATAGAGCACTGTGGAAACACAGAGGAGGGGGTGGAAAAAGTCAGGGA GTGCTCTGATGAAGTAAAATAGAGCACTGTGGGAACACAGAGGAGGGGGTGGAAAAAGTCAGGGA T C KAT6A Ensembl:ENSG00000083168 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:42033622..42033714 26863196 MeRIP-seq:(Medium) rs1020550702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115175,RMVar_hsa_circ_251556,RMVar_hsa_circ_347690,RMVar_hsa_circ_101677,RMVar_hsa_circ_267962,RMVar_hsa_circ_251565 110135 RMVar_ID_110135 Human_SNP_ID_360752469 m1A Human chr8 + 42153104 42153104 42153104 TAGGAGCAGTGGGCGCTGAGAGCAGCAAGGCCAGGTGAGGAGTAGGGACGACCCCGAGCCTGGAG TAGGAGCAGTGGGCGCTGAGAGCAGCAAGGCCGGGTGAGGAGTAGGGACGACCCCGAGCCTGGAG A G AP3M2 Ensembl:ENSG00000070718 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:42153091..42153212;chr8:42153073..42153223 26863196 MeRIP-seq:(Medium) rs1018571845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18426823,Human_RBP_ID_19141147 Human_Splice_Rec_970697,Human_Splice_Rec_970739,Human_Splice_Rec_970743,Human_Splice_Rec_970759,Human_Splice_Rec_970773 110136 RMVar_ID_110136 Human_SNP_ID_360757006 m1A Human chr8 + 42170088 42170088 42170088 GAAGGTGAGCACAGCTGTGAGTGAGTGAGCTCATATCTCCATTTGTCAGTGCTGGACTGGTACCA GAAGGTGAGCACAGCTGTGAGTGAGTGAGCTCGTATCTCCATTTGTCAGTGCTGGACTGGTACCA A G AP3M2 Ensembl:ENSG00000070718 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:42170044..42170145 32194978 MeRIP-seq:(Medium) rs574499529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9225177,Human_RBP_ID_16417642 RMVar_hsa_circ_107492,RMVar_hsa_circ_110403,RMVar_hsa_circ_251567,RMVar_hsa_circ_89998,RMVar_hsa_circ_251568,RMVar_hsa_circ_86988,RMVar_hsa_circ_251569,RMVar_hsa_circ_251570 110137 RMVar_ID_110137 Human_SNP_ID_360763607 m1A Human chr8 - 42193213 42193213 42193213 CCCCGTGATCAAGCTGTTTTTTCTCTCCTTCCAGAATTTAAGGGACGCTGTGAAGCAATCATGGA CCCCGTGATCAAGCTGTTTTTTCTCTCCTTCCTGAATTTAAGGGACGCTGTGAAGCAATCATGGA T A PLAT Ensembl:ENSG00000104368 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:42193170..42193253 26863196 MeRIP-seq:(Medium) rs1554498594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_970837,Human_Splice_Rec_970865,Human_Splice_Rec_970891,Human_Splice_Rec_970915,Human_Splice_Rec_970939,Human_Splice_Rec_970959,Human_Splice_Rec_970997,Human_Splice_Rec_971007 110138 RMVar_ID_110138 Human_SNP_ID_360783940 m1A Human chr8 - 42271448 42271448 42271448 GGGGGACTCACCTGTCGGCAGGGACGCGGGGCAGGGGGCGGGCTCCCCGGGGCGGGGAAGGCGGG GGGGGACTCACCTGTCGGCAGGGACGCGGGGCGGGGGGCGGGCTCCCCGGGGCGGGGAAGGCGGG T C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:42271343..42271469 26863196 MeRIP-seq:(Medium) rs565023239 Functional Loss SNV dbSNP153 33..33 33 - - - 110139 RMVar_ID_110139 Human_SNP_ID_360784111 m1A Human chr8 + 42272052 42272052 42272052 TCCCTTTGAGCTCCATTTTTTTCTTAATCCTAACCTTTTTTCCCCATCCCAAATTGCTTATAGAG TCCCTTTGAGCTCCATTTTTTTCTTAATCCTAGCCTTTTTTCCCCATCCCAAATTGCTTATAGAG A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:42272042..42272159 26863196 MeRIP-seq:(Medium) rs1032591323 Functional Loss SNV dbSNP153 33..33 33 - - - 110140 RMVar_ID_110140 Human_SNP_ID_360801032 m1A Human chr8 - 42342316 42342316 42342316 TGCAACATATTGTACTGGCCTGCTGCTGGCCCACAGGCTTCTCAATAGGTTTGGCATGGACAAGA TGCAACATATTGTACTGGCCTGCTGCTGGCCCGCAGGCTTCTCAATAGGTTTGGCATGGACAAGA T C RPL5P23 Ensembl:ENSG00000240395 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879141985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_699917 Human_miRNA_ID_1877298,Human_miRNA_ID_1878908 110141 RMVar_ID_110141 Human_SNP_ID_360801041 m1A Human chr8 - 42342344 42342344 42342344 GTGTGAAGGTTGGCCTGACAAATTATGCTGCAACATATTGTACTGGCCTGCTGCTGGCCCACAGG GTGTGAAGGTTGGCCTGACAAATTATGCTGCAGCATATTGTACTGGCCTGCTGCTGGCCCACAGG T C RPL5P23 Ensembl:ENSG00000240395 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879032377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1830899,Human_miRNA_ID_1836339,Human_miRNA_ID_1841465,Human_miRNA_ID_1862958,Human_miRNA_ID_1878738,Human_miRNA_ID_1882892,Human_miRNA_ID_1908692,Human_miRNA_ID_1909253 110142 RMVar_ID_110142 Human_SNP_ID_360816083 m1A Human chr8 - 42401881 42401881 42401881 AGCCACCCTTCGAAGGCCAACACAGCCCAGCCATAGATGGTTGGTCCAGAAAAATCTATATCAAC AGCCACCCTTCGAAGGCCAACACAGCCCAGCCGTAGATGGTTGGTCCAGAAAAATCTATATCAAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:42401832..42401983 32194978 MeRIP-seq:(Medium) rs202057696 Functional Loss SNV dbSNP153 33..33 33 - - - 110143 RMVar_ID_110143 Human_SNP_ID_360845066 m1A Human chr8 + 42519401 42519401 42519401 GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAG GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAG A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr8:42519375..42519459 26863410 MeRIP-seq:(Medium) rs1267371394 Functional Loss SNV dbSNP153 33..33 33 - - - 110144 RMVar_ID_110144 Human_SNP_ID_360848847 m1A Human chr8 - 42533784 42533784 42533784 CATGGTGGTGCACGCCTGTAATCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG CATGGTGGTGCACGCCTGTAATCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1048647039 Functional Loss SNV dbSNP153 33..33 33 - - - 110145 RMVar_ID_110145 Human_SNP_ID_360848924 m1A Human chr8 - 42533970 42533970 42533970 AAGCAGGGATTTCTTCAAATGCTAGTAAGCACAAAGAGAGGGAGAAGTTTTTGTAAGTAACGAAC AAGCAGGGATTTCTTCAAATGCTAGTAAGCACTAAGAGAGGGAGAAGTTTTTGTAAGTAACGAAC T A SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:42533924..42534010 26863196 MeRIP-seq:(Medium) rs1200360723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23199549 110146 RMVar_ID_110146 Human_SNP_ID_360850851 m1A Human chr8 + 42541671 42541671 42541671 CGACTCCGGGGTAAAGAGCCCCGGAGCGGAGCAGCGCTGGCCGCGTGCCGCCTCCGGAGCCGGCA CGACTCCGGGGTAAAGAGCCCCGGAGCGGAGCCGCGCTGGCCGCGTGCCGCCTCCGGAGCCGGCA A C SMIM19 Ensembl:ENSG00000176209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:42541621..42541735 26863196 MeRIP-seq:(Medium) rs1033526128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4986355 Human_Splice_Rec_972169,Human_Splice_Rec_972177,Human_Splice_Rec_972183 110147 RMVar_ID_110147 Human_SNP_ID_360850852 m1A Human chr8 + 42541671 42541671 42541671 CGACTCCGGGGTAAAGAGCCCCGGAGCGGAGCAGCGCTGGCCGCGTGCCGCCTCCGGAGCCGGCA CGACTCCGGGGTAAAGAGCCCCGGAGCGGAGCGGCGCTGGCCGCGTGCCGCCTCCGGAGCCGGCA A G SMIM19 Ensembl:ENSG00000176209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:42541621..42541735 26863196 MeRIP-seq:(Medium) rs1033526128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4986355 Human_Splice_Rec_972169,Human_Splice_Rec_972177,Human_Splice_Rec_972183 110148 RMVar_ID_110148 Human_SNP_ID_360938402 m1A Human chr8 + 42887847 42887847 42887847 GAATCATCATCCAGTTTCAAACTTTGAACTTCACCTTGATATTTGGCCATTCCAGGTCTAAAATA GAATCATCATCCAGTTTCAAACTTTGAACTTCCCCTTGATATTTGGCCATTCCAGGTCTAAAATA A C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:42887798..42887915 26863196 MeRIP-seq:(Medium) rs751443204 Functional Loss SNV dbSNP153 33..33 33 - - - 110149 RMVar_ID_110149 Human_SNP_ID_360940735 m1A Human chr8 - 42896535 42896535 42896535 CGGGAGGGGTGGCGGGAGCGGTCCTGGAAATAATCTGTCCTCTGTCGCCGGGAACTGGCGAGGTA CGGGAGGGGTGGCGGGAGCGGTCCTGGAAATAGTCTGTCCTCTGTCGCCGGGAACTGGCGAGGTA T C RNF170 Ensembl:ENSG00000120925 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:42896482..42896701 26863196 MeRIP-seq:(Medium) rs756895561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_960206,Human_RBP_ID_4986472,Human_RBP_ID_5453526,Human_RBP_ID_5514871,Human_RBP_ID_18426691,Human_RBP_ID_22626331 Human_Splice_Rec_972277,Human_Splice_Rec_972299,Human_Splice_Rec_972321,Human_Splice_Rec_972333,Human_Splice_Rec_972343,Human_Splice_Rec_972353 RMVar_hsa_circ_83256,RMVar_hsa_circ_251652 110150 RMVar_ID_110150 Human_SNP_ID_360941062 m1A Human chr8 - 42897067 42897067 42897067 CTGGCCAGACACCGCCGCCGCTCTGTCGGGGGATCCGGGGGCCCGCGCAGCTGACTCGGCCTCAG CTGGCCAGACACCGCCGCCGCTCTGTCGGGGGGTCCGGGGGCCCGCGCAGCTGACTCGGCCTCAG T C RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:42897005..42897171 26863196 MeRIP-seq:(Medium) rs556821402 Functional Loss SNV dbSNP153 33..33 33 - - - 110151 RMVar_ID_110151 Human_SNP_ID_360941063 m1A Human chr8 - 42897067 42897067 42897067 CTGGCCAGACACCGCCGCCGCTCTGTCGGGGGATCCGGGGGCCCGCGCAGCTGACTCGGCCTCAG CTGGCCAGACACCGCCGCCGCTCTGTCGGGGGCTCCGGGGGCCCGCGCAGCTGACTCGGCCTCAG T G RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:42897005..42897171 26863196 MeRIP-seq:(Medium) rs556821402 Functional Loss SNV dbSNP153 33..33 33 - - - 110152 RMVar_ID_110152 Human_SNP_ID_360972823 m1A Human chr8 + 43020991 43020991 43020991 AGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGAGGGTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTGCTTGGGAGGGTGAGGCAGGAGAATTGCTTGAA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs188146832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 110153 RMVar_ID_110153 Human_SNP_ID_360981921 m1A Human chr8 + 43056381 43056381 43056381 GGCGGCCACCGAGGGGGTCGGGGAGGCTGCGCAAGGGGGCGAGCCCGGGCAGCCGGCGCAACCCC GGCGGCCACCGAGGGGGTCGGGGAGGCTGCGCGAGGGGGCGAGCCCGGGCAGCCGGCGCAACCCC A G FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:43056354..43056480 26863196 MeRIP-seq:(Medium) rs1240137085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255029,Human_RBP_ID_961126,Human_RBP_ID_4995475,Human_RBP_ID_9338263 RMVar_hsa_circ_93420,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_251726 110154 RMVar_ID_110154 Human_SNP_ID_360981952 m1A Human chr8 + 43056426 43056426 43056426 CGGGCAGCCGGCGCAACCCCCGCCCCAGCCGCACCCACCGCCGCCCCAGCAGCAGCACAAGGAAG CGGGCAGCCGGCGCAACCCCCGCCCCAGCCGCTCCCACCGCCGCCCCAGCAGCAGCACAAGGAAG A T FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:43056375..43056489 26863196 MeRIP-seq:(Medium) rs1563324180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795952,Human_RBP_ID_9338641,Human_RBP_ID_26765753 Human_Splice_Rec_972559 RMVar_hsa_circ_93420,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_251726 110155 RMVar_ID_110155 Human_SNP_ID_360991934 m1A Human chr8 - 43093554 43093554 43093554 TCACCCCTCGCCGCAGCACCTACCTGCAGCCCAAGCCTCTGCGGCTCCTGCCACCCCGGGCCAGC TCACCCCTCGCCGCAGCACCTACCTGCAGCCCGAGCCTCTGCGGCTCCTGCCACCCCGGGCCAGC T C RF00017-1264 RNACentral:URS00009A773B SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:43093538..43093627 26863196 MeRIP-seq:(Medium) rs999343235 Functional Loss SNV dbSNP153 33..33 33 - - - 110156 RMVar_ID_110156 Human_SNP_ID_361004178 m1A Human chr8 + 43140483 43140475 43140483 GGCGGGGCGCAGCGGGCAGGCAAGGGCGGCCGAGCGGGCGGCGGGCATGAGCGGGGCGGGCAGGG GGCGGGGCGCAGCGGGCAGGCAAGG________GCGGGCGGCGGGCATGAGCGGGGCGGGCAGGG GGCGGCCGA G HGSNAT Ensembl:ENSG00000165102 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:43140404..43140579 26863196 MeRIP-seq:(Medium) rs1313661816 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_4995039 RMVar_hsa_circ_251751,RMVar_hsa_circ_95383 110157 RMVar_ID_110157 Human_SNP_ID_361004184 m1A Human chr8 + 43140483 43140483 43140483 GGCGGGGCGCAGCGGGCAGGCAAGGGCGGCCGAGCGGGCGGCGGGCATGAGCGGGGCGGGCAGGG GGCGGGGCGCAGCGGGCAGGCAAGGGCGGCCGGGCGGGCGGCGGGCATGAGCGGGGCGGGCAGGG A G HGSNAT Ensembl:ENSG00000165102 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:43140404..43140579 26863196 MeRIP-seq:(Medium) rs1396219966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4995039 RMVar_hsa_circ_251751,RMVar_hsa_circ_95383 110158 RMVar_ID_110158 Human_SNP_ID_361004236 m1A Human chr8 - 43140592 43140592 43140592 GTGCACTCACCTCGTGGCGGCGCGGCCTGGGCATCGCGCCCCGAAGAGCCGCCGGGGGCCAGCAG GTGCACTCACCTCGTGGCGGCGCGGCCTGGGCTTCGCGCCCCGAAGAGCCGCCGGGGGCCAGCAG T A RF00017-1264 RNACentral:URS00009A773B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:43140397..43140667 26863196 MeRIP-seq:(Medium) rs1348055539 Functional Loss SNV dbSNP153 33..33 33 - - - 110159 RMVar_ID_110159 Human_SNP_ID_361018310 m1A Human chr8 + 43195774 43195746 43195775 AGGAAGAGGAGGAGGAGGGGTAGAGGAAGAAGAGGAGGAGGAGGGTGTGGAAGAGGAGTAGGGGT AGGAA_____________________________GAGGAGGAGGGTGTGGAAGAGGAGTAGGGGT AGAGGAGGAGGAGGGGTAGAGGAAGAAGAG A HGSNAT Ensembl:ENSG00000165102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:43195724..43195908 26863196 MeRIP-seq:(Medium) rs1563385141 Functional Loss DEL dbSNP153 6..34 33 - - - Human_RBP_ID_846017,Human_RBP_ID_5224708,Human_RBP_ID_8221074,Human_RBP_ID_9441117 RMVar_hsa_circ_20508,RMVar_hsa_circ_251766,RMVar_hsa_circ_251767,RMVar_hsa_circ_328601,RMVar_hsa_circ_251769,RMVar_hsa_circ_335054,RMVar_hsa_circ_4805,RMVar_hsa_circ_298363 110160 RMVar_ID_110160 Human_SNP_ID_361018322 m1A Human chr8 + 43195774 43195772 43195775 AGGAAGAGGAGGAGGAGGGGTAGAGGAAGAAGAGGAGGAGGAGGGTGTGGAAGAGGAGTAGGGGT AGGAAGAGGAGGAGGAGGGGTAGAGGAAGAA___GAGGAGGAGGGTGTGGAAGAGGAGTAGGGGT AGAG A HGSNAT Ensembl:ENSG00000165102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:43195724..43195908 26863196 MeRIP-seq:(Medium) rs753437318 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_846017,Human_RBP_ID_5224708,Human_RBP_ID_8221074,Human_RBP_ID_9441117 RMVar_hsa_circ_20508,RMVar_hsa_circ_251766,RMVar_hsa_circ_251767,RMVar_hsa_circ_328601,RMVar_hsa_circ_251769,RMVar_hsa_circ_335054,RMVar_hsa_circ_4805,RMVar_hsa_circ_298363 110161 RMVar_ID_110161 Human_SNP_ID_361018501 m1A Human chr8 + 43196470 43196470 43196470 AGACTGGGTCACCAAACAGGCCTGTCTGACGGAACCCTTGTCACCTTTGTGGAGAATTCTCTTTG AGACTGGGTCACCAAACAGGCCTGTCTGACGGCACCCTTGTCACCTTTGTGGAGAATTCTCTTTG A C HGSNAT Ensembl:ENSG00000165102 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:43196384..43196731 26863196 MeRIP-seq:(Medium) rs1177905533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16423302 Human_Splice_Rec_972714,Human_Splice_Rec_972715 RMVar_hsa_circ_20508,RMVar_hsa_circ_251766,RMVar_hsa_circ_251767,RMVar_hsa_circ_328601,RMVar_hsa_circ_251769,RMVar_hsa_circ_335054,RMVar_hsa_circ_4805,RMVar_hsa_circ_298363 110162 RMVar_ID_110162 Human_SNP_ID_361018505 m1A Human chr8 - 43196487 43196487 43196487 TACTTCCAGGCAGGGCCCAAAGAGAATTCTCCACAAAGGTGACAAGGGTTCCGTCAGACAGGCCT TACTTCCAGGCAGGGCCCAAAGAGAATTCTCCGCAAAGGTGACAAGGGTTCCGTCAGACAGGCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:43196445..43196631 26863196 MeRIP-seq:(Medium) rs1420835402 Functional Loss SNV dbSNP153 33..33 33 - - - 110163 RMVar_ID_110163 Human_SNP_ID_361019725 m1A Human chr8 - 43201356 43201356 43201356 GATGGGGAGGTGGAGGAGAGAGCAGGGAGTGGAGTGGGAGGGGAGGCTGGAAAGATGTGTGGGGA GATGGGGAGGTGGAGGAGAGAGCAGGGAGTGGCGTGGGAGGGGAGGCTGGAAAGATGTGTGGGGA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:43201307..43201450 26863196 MeRIP-seq:(Medium) rs1361177188 Functional Loss SNV dbSNP153 33..33 33 - - - 110164 RMVar_ID_110164 Human_SNP_ID_318941881 m1A Human chr7 + 45000334 45000334 45000334 CCGGGCGGGCCGCGGGAGCCGCACGCGGCGATATGGAAGAGGAGGGCAAGAAGGGCAAGAAGGTG CCGGGCGGGCCGCGGGAGCCGCACGCGGCGATGTGGAAGAGGAGGGCAAGAAGGGCAAGAAGGTG A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:45000246..45000357 26863410 MeRIP-seq:(Medium) rs137852842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956339,Human_RBP_ID_9337776,Human_RBP_ID_9439246,Human_RBP_ID_18426525 Human_Splice_Rec_864241,Human_Splice_Rec_864255,Human_Splice_Rec_864271,Human_Splice_Rec_864285,Human_Splice_Rec_864303,Human_Splice_Rec_864319 Clinvar_Rec_738 110165 RMVar_ID_110165 Human_SNP_ID_318941884 m1A Human chr7 + 45000344 45000344 45000344 CGCGGGAGCCGCACGCGGCGATATGGAAGAGGAGGGCAAGAAGGGCAAGAAGGTGAGCGTGCGCG CGCGGGAGCCGCACGCGGCGATATGGAAGAGGGGGGCAAGAAGGGCAAGAAGGTGAGCGTGCGCG A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:44999764..45027053;chr7:45000195..45000422 26863196 MeRIP-seq:(Medium) rs868489016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4956339,Human_RBP_ID_9337776,Human_RBP_ID_9439711 Human_Splice_Rec_864241,Human_Splice_Rec_864255,Human_Splice_Rec_864271,Human_Splice_Rec_864285,Human_Splice_Rec_864303,Human_Splice_Rec_864319 110166 RMVar_ID_110166 Human_SNP_ID_318952031 m1A Human chr7 + 45038301 45038301 45038301 CATTTAAACGAGTATTCCTAAAAGGTGAAAAGAGTAGAGATAAGAAAGCCCATGAGAAGGTGACA CATTTAAACGAGTATTCCTAAAAGGTGAAAAGTGTAGAGATAAGAAAGCCCATGAGAAGGTGACA A T CCM2 Ensembl:ENSG00000136280 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:45029497..45038425;chr7:45038201..45038388 26863196 MeRIP-seq:(Medium) rs1462817923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685185,Human_RBP_ID_4956340 Human_Splice_Rec_864224,Human_Splice_Rec_864242,Human_Splice_Rec_864274,Human_Splice_Rec_864286,Human_Splice_Rec_864304,Human_Splice_Rec_864320,Human_Splice_Rec_864346,Human_Splice_Rec_864364,Human_Splice_Rec_864392,Human_Splice_Rec_864400,Human_Splice_Rec_864408,Human_Splice_Rec_864422 RMVar_hsa_circ_245030,RMVar_hsa_circ_295743 110167 RMVar_ID_110167 Human_SNP_ID_318958643 m1A Human chr7 + 45064562 45064562 45064562 ACGTCAAGCTGGCCTGGAGGGACGGGGAGGATATCATCCTCAGGGTGCCCATCCATGACATCGCC ACGTCAAGCTGGCCTGGAGGGACGGGGAGGATGTCATCCTCAGGGTGCCCATCCATGACATCGCC A G CCM2 Ensembl:ENSG00000136280 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:45064513..45064591 26863196 MeRIP-seq:(Medium) rs1418279801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26830348 Human_Splice_Rec_864228,Human_Splice_Rec_864229,Human_Splice_Rec_864246,Human_Splice_Rec_864247,Human_Splice_Rec_864258,Human_Splice_Rec_864259,Human_Splice_Rec_864278,Human_Splice_Rec_864279,Human_Splice_Rec_864290,Human_Splice_Rec_864291,Human_Splice_Rec_864308,Human_Splice_Rec_864309,Human_Splice_Rec_864324,Human_Splice_Rec_864325,Human_Splice_Rec_864344,Human_Splice_Rec_864350,Human_Splice_Rec_864351,Human_Splice_Rec_864368,Human_Splice_Rec_864369,Human_Splice_Rec_864384,Human_Splice_Rec_864385,Human_Splice_Rec_864394,Human_Splice_Rec_864395,Human_Splice_Rec_864412,Human_Splice_Rec_864413,Human_Splice_Rec_864426,Human_Splice_Rec_864427,Human_Splice_Rec_864436,Human_Splice_Rec_864437 Human_miRNA_ID_121867,Human_miRNA_ID_125684,Human_miRNA_ID_1972749,Human_miRNA_ID_1974926,Human_miRNA_ID_2466186,Human_miRNA_ID_2612741 RMVar_hsa_circ_245031,RMVar_hsa_circ_280321,RMVar_hsa_circ_245030,RMVar_hsa_circ_295743,RMVar_hsa_circ_290168,RMVar_hsa_circ_245032 110168 RMVar_ID_110168 Human_SNP_ID_318959995 m1A Human chr7 + 45069892 45069892 45069892 AGGTCTTCCAGGTTGTTTACACGGAGTCCACCATCGACTTTCTGGACAGAGCGATATTTGATGGG AGGTCTTCCAGGTTGTTTACACGGAGTCCACCGTCGACTTTCTGGACAGAGCGATATTTGATGGG A G CCM2 Ensembl:ENSG00000136280 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:45068457..45070004 32194978 MeRIP-seq:(Medium) rs374628317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_864232,Human_Splice_Rec_864233,Human_Splice_Rec_864262,Human_Splice_Rec_864263,Human_Splice_Rec_864280,Human_Splice_Rec_864281,Human_Splice_Rec_864294,Human_Splice_Rec_864295,Human_Splice_Rec_864312,Human_Splice_Rec_864313,Human_Splice_Rec_864328,Human_Splice_Rec_864329,Human_Splice_Rec_864354,Human_Splice_Rec_864355,Human_Splice_Rec_864372,Human_Splice_Rec_864373,Human_Splice_Rec_864388,Human_Splice_Rec_864389,Human_Splice_Rec_864396,Human_Splice_Rec_864397,Human_Splice_Rec_864404,Human_Splice_Rec_864405,Human_Splice_Rec_864430,Human_Splice_Rec_864431,Human_Splice_Rec_864438,Human_Splice_Rec_864442,Human_Splice_Rec_864443,Human_Splice_Rec_864452,Human_Splice_Rec_864453 RMVar_hsa_circ_280321,RMVar_hsa_circ_245032,RMVar_hsa_circ_333945 110169 RMVar_ID_110169 Human_SNP_ID_318962748 m1A Human chr7 + 45078776 45078776 45078776 TGAGGGGACATCAGTAATGAGGGGACGTCAGAAGGCGGTGAGGGGACACCAGAGAGTAATGGGAC TGAGGGGACATCAGTAATGAGGGGACGTCAGATGGCGGTGAGGGGACACCAGAGAGTAATGGGAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:45078774..45078839 26863196 MeRIP-seq:(Medium) rs1170032411 Functional Loss SNV dbSNP153 33..33 33 - - - 110170 RMVar_ID_110170 Human_SNP_ID_318970321 m1A Human chr7 + 45104202 45104202 45104202 CCTCACCAGAAGTCAGGCTGGGCATGAGGGATAGCAGGTCGGTGGCCAGGCGCTGGGACACCTGG CCTCACCAGAAGTCAGGCTGGGCATGAGGGATGGCAGGTCGGTGGCCAGGCGCTGGGACACCTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:45104151..45104225 32194978 MeRIP-seq:(Medium) rs747109085 Functional Loss SNV dbSNP153 33..33 33 - - - 110171 RMVar_ID_110171 Human_SNP_ID_318970341 m1A Human chr7 - 45104248 45104248 45104248 CCTGTGATCTGCTCTGTCCTGAAGGCAAACTCAGCTTTCACCAGACCCAGGTGTCCCAGCGCCTG CCTGTGATCTGCTCTGTCCTGAAGGCAAACTCTGCTTTCACCAGACCCAGGTGTCCCAGCGCCTG T A TBRG4 Ensembl:ENSG00000136270 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:45104139..45104625 32194978 MeRIP-seq:(Medium) rs771569133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685227,Human_RBP_ID_956950 Human_Splice_Rec_864482,Human_Splice_Rec_864530,Human_Splice_Rec_864550,Human_Splice_Rec_864580,Human_Splice_Rec_864586,Human_Splice_Rec_864594 Human_miRNA_ID_2406015,Human_miRNA_ID_2409010,Human_miRNA_ID_2411997,Human_miRNA_ID_2414974,Human_miRNA_ID_2623486 RMVar_hsa_circ_127371,RMVar_hsa_circ_76419,RMVar_hsa_circ_99964,RMVar_hsa_circ_92636,RMVar_hsa_circ_245039,RMVar_hsa_circ_245040,RMVar_hsa_circ_245041,RMVar_hsa_circ_297643,RMVar_hsa_circ_122474,RMVar_hsa_circ_245042,RMVar_hsa_circ_245043,RMVar_hsa_circ_77404,RMVar_hsa_circ_313896,RMVar_hsa_circ_245044,RMVar_hsa_circ_245046,RMVar_hsa_circ_119570,RMVar_hsa_circ_245045 110172 RMVar_ID_110172 Human_SNP_ID_318970342 m1A Human chr7 - 45104248 45104248 45104248 CCTGTGATCTGCTCTGTCCTGAAGGCAAACTCAGCTTTCACCAGACCCAGGTGTCCCAGCGCCTG CCTGTGATCTGCTCTGTCCTGAAGGCAAACTCGGCTTTCACCAGACCCAGGTGTCCCAGCGCCTG T C TBRG4 Ensembl:ENSG00000136270 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:45104139..45104625 32194978 MeRIP-seq:(Medium) rs771569133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685227,Human_RBP_ID_956950 Human_Splice_Rec_864482,Human_Splice_Rec_864530,Human_Splice_Rec_864550,Human_Splice_Rec_864580,Human_Splice_Rec_864586,Human_Splice_Rec_864594 Human_miRNA_ID_2406015,Human_miRNA_ID_2409010,Human_miRNA_ID_2411997,Human_miRNA_ID_2414974,Human_miRNA_ID_2623486 RMVar_hsa_circ_127371,RMVar_hsa_circ_76419,RMVar_hsa_circ_99964,RMVar_hsa_circ_92636,RMVar_hsa_circ_245039,RMVar_hsa_circ_245040,RMVar_hsa_circ_245041,RMVar_hsa_circ_297643,RMVar_hsa_circ_122474,RMVar_hsa_circ_245042,RMVar_hsa_circ_245043,RMVar_hsa_circ_77404,RMVar_hsa_circ_313896,RMVar_hsa_circ_245044,RMVar_hsa_circ_245046,RMVar_hsa_circ_119570,RMVar_hsa_circ_245045 110173 RMVar_ID_110173 Human_SNP_ID_318970871 m1A Human chr7 - 45105643 45105643 45105643 GGTGGAGCAGGAGGTCCGCTGGCGCATGCGGAAGCTCAAGTACAAGCACCTGGCCTTCCTGGCAG GGTGGAGCAGGAGGTCCGCTGGCGCATGCGGAGGCTCAAGTACAAGCACCTGGCCTTCCTGGCAG T C TBRG4 Ensembl:ENSG00000136270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:45105410..45105701 26863196 MeRIP-seq:(Medium) rs955718453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9404440 RMVar_hsa_circ_76419,RMVar_hsa_circ_92636,RMVar_hsa_circ_245040,RMVar_hsa_circ_245041,RMVar_hsa_circ_245047,RMVar_hsa_circ_122474,RMVar_hsa_circ_77404,RMVar_hsa_circ_245044,RMVar_hsa_circ_245046,RMVar_hsa_circ_372835 110174 RMVar_ID_110174 Human_SNP_ID_318971756 m1A Human chr7 + 45109105 45109105 45109105 CATCAAGGAACCTGGGAGGTGGGAAATGGGTGAGGTGGCTGAGGAAGTCAGAGTCTTATGGGCTA CATCAAGGAACCTGGGAGGTGGGAAATGGGTGGGGTGGCTGAGGAAGTCAGAGTCTTATGGGCTA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:45108851..45110763 32194978 MeRIP-seq:(Medium) rs541547355 Functional Loss SNV dbSNP153 33..33 33 - - - 110175 RMVar_ID_110175 Human_SNP_ID_318971766 m1A Human chr7 + 45109141 45109141 45109141 GGCTGAGGAAGTCAGAGTCTTATGGGCTACCCAGGCAAGTCTCAGTCGGCCAACTGGAGCCATGG GGCTGAGGAAGTCAGAGTCTTATGGGCTACCCGGGCAAGTCTCAGTCGGCCAACTGGAGCCATGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:45109090..45109237 26863196 MeRIP-seq:(Medium) rs751369063 Functional Loss SNV dbSNP153 33..33 33 - - - 110176 RMVar_ID_110176 Human_SNP_ID_318971824 m1A Human chr7 - 45109289 45109285 45109290 GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTTCAGGGTTTGGAATCACTTGCTAGGAGTCTTGTCT GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTT_____TTTGGAATCACTTGCTAGGAGTCTTGTCT ACCCTG A TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:45109251..45109300 26863196 MeRIP-seq:(Medium) rs1453737852 Functional Loss DEL dbSNP153 32..36 33 - - - Human_Splice_Rec_864597 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 110177 RMVar_ID_110177 Human_SNP_ID_318971826 m1A Human chr7 - 45109289 45109289 45109289 GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTTCAGGGTTTGGAATCACTTGCTAGGAGTCTTGTCT GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTTCTGGGTTTGGAATCACTTGCTAGGAGTCTTGTCT T A TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:45109251..45109300 26863196 MeRIP-seq:(Medium) rs113918945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_864597 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 110178 RMVar_ID_110178 Human_SNP_ID_318971827 m1A Human chr7 - 45109289 45109289 45109289 GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTTCAGGGTTTGGAATCACTTGCTAGGAGTCTTGTCT GTAGTAGCCCCTTCTCTCTCCTTTTTCTCTTCGGGGTTTGGAATCACTTGCTAGGAGTCTTGTCT T C TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:45109251..45109300 26863196 MeRIP-seq:(Medium) rs113918945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_864597 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 110179 RMVar_ID_110179 Human_SNP_ID_318972452 m1A Human chr7 - 45111445 45111445 45111445 GTGCGCACGCTTCCTCTCTAGCCCGCGCGGCCAGGCCTGGAAGACGCCGCCCCTGTTGACCGTCC GTGCGCACGCTTCCTCTCTAGCCCGCGCGGCCGGGCCTGGAAGACGCCGCCCCTGTTGACCGTCC T C TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:45111441..45111725 26863196 MeRIP-seq:(Medium) rs931323364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_864611 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 110180 RMVar_ID_110180 Human_SNP_ID_318972549 m1A Human chr7 - 45111665 45111665 45111665 ATGGTTCCGGGGACAGTTAGGGCGGCGGATGGAGGTCAGCGGTGGTGCTCGCTGCGTAGGTCTTG ATGGTTCCGGGGACAGTTAGGGCGGCGGATGGTGGTCAGCGGTGGTGCTCGCTGCGTAGGTCTTG T A TBRG4 Ensembl:ENSG00000136270 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:45111534..45111672 26863196 MeRIP-seq:(Medium) rs1373793298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_793539,Human_RBP_ID_843962,Human_RBP_ID_4956341,Human_RBP_ID_5429593,Human_RBP_ID_9311284,Human_RBP_ID_17664513,Human_RBP_ID_18101257,Human_RBP_ID_18425999,Human_RBP_ID_22463089,Human_RBP_ID_22622879,Human_RBP_ID_26356455 Human_Splice_Rec_864475,Human_Splice_Rec_864495,Human_Splice_Rec_864511,Human_Splice_Rec_864543,Human_Splice_Rec_864587,Human_Splice_Rec_864595,Human_Splice_Rec_864605,Human_Splice_Rec_864613 Human_miRNA_ID_2300036,Human_miRNA_ID_2303303,Human_miRNA_ID_2306568 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 110181 RMVar_ID_110181 Human_SNP_ID_319008252 m1A Human chr7 - 45252018 45252018 45252018 ACAGGCGGGGTAAGATTTGCCGAGTTCCTTTTACTTTTTTTAACCTTTCCTTATAAGCATGCCTG ACAGGCGGGGTAAGATTTGCCGAGTTCCTTTTGCTTTTTTTAACCTTTCCTTATAAGCATGCCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:45251950..45252066 26863196 MeRIP-seq:(Medium) rs1046565170 Functional Loss SNV dbSNP153 33..33 33 - - - 110182 RMVar_ID_110182 Human_SNP_ID_319170615 m1A Human chr7 + 45912501 45912501 45912501 GAATGTCTTGAGACCCCTCTGTTTTCAAGGAGAGCTCTATGCAGCGTGTGTCCACACCGAGGTCT GAATGTCTTGAGACCCCTCTGTTTTCAAGGAGCGCTCTATGCAGCGTGTGTCCACACCGAGGTCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:45912451..45912550 32194978 MeRIP-seq:(Medium) rs550285802 Functional Loss SNV dbSNP153 33..33 33 - - - 110183 RMVar_ID_110183 Human_SNP_ID_319170768 m1A Human chr7 + 45913101 45913101 45913101 GACTCTCCCTGTCTCTCTGTCCCTCCTACCCCACGGGGCCGCAGCAAAAGCCATCCTGGGCCTTC GACTCTCCCTGTCTCTCTGTCCCTCCTACCCCGCGGGGCCGCAGCAAAAGCCATCCTGGGCCTTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:45913054..45913267 26863196 MeRIP-seq:(Medium) rs1286692569 Functional Loss SNV dbSNP153 33..33 33 - - - 110184 RMVar_ID_110184 Human_SNP_ID_319527396 m1A Human chr7 - 47325236 47325236 47325236 GTGGGATGCCTGGCTTTCTTGAGTGACCAAGTACAGATAGAAAAGCTTCTAGAATGCTATGGAAC GTGGGATGCCTGGCTTTCTTGAGTGACCAAGTGCAGATAGAAAAGCTTCTAGAATGCTATGGAAC T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47325234..47325378 26863196 MeRIP-seq:(Medium) rs1474777005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37444,RMVar_hsa_circ_79363,RMVar_hsa_circ_245072,RMVar_hsa_circ_61351,RMVar_hsa_circ_342919 110185 RMVar_ID_110185 Human_SNP_ID_319533907 m1A Human chr7 + 47352028 47352028 47352028 ACTCTCACGTGGTCTCTTACACACATTTTCTCATAACACTCATGCAGACTCAGCCACTCATGCAT ACTCTCACGTGGTCTCTTACACACATTTTCTCGTAACACTCATGCAGACTCAGCCACTCATGCAT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:47351987..47352116 26863196 MeRIP-seq:(Medium) rs1053849958 Functional Loss SNV dbSNP153 33..33 33 - - - 110186 RMVar_ID_110186 Human_SNP_ID_319533964 m1A Human chr7 - 47352159 47352157 47352159 CTGCTTGTGACTGTTGTGTGAATGTGGGTGAGAGTGTTAGTGCAAGGGTGTGTGAGTGTAAGAGT CTGCTTGTGACTGTTGTGTGAATGTGGGTGAG__TGTTAGTGCAAGGGTGTGTGAGTGTAAGAGT ACT A TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:47351900..47352222 26863196 MeRIP-seq:(Medium) rs1245348708 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5305859,Human_RBP_ID_17316036,Human_RBP_ID_23116652,Human_RBP_ID_24217482 RMVar_hsa_circ_37444,RMVar_hsa_circ_54228,RMVar_hsa_circ_340637,RMVar_hsa_circ_366242,RMVar_hsa_circ_351428,RMVar_hsa_circ_331230,RMVar_hsa_circ_58880 110187 RMVar_ID_110187 Human_SNP_ID_319534018 m1A Human chr7 - 47352340 47352340 47352340 TGTGAGTGTGAGAATGAGTGTGAGACTGTGTGAGGCTGTCTGTGAGTGTACAAGACTGAGACTGA TGTGAGTGTGAGAATGAGTGTGAGACTGTGTGCGGCTGTCTGTGAGTGTACAAGACTGAGACTGA T G TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:47352305..47352407 26863196 MeRIP-seq:(Medium) rs1459477289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5305860,Human_RBP_ID_17315587,Human_RBP_ID_23116653,Human_RBP_ID_24217487 RMVar_hsa_circ_37444,RMVar_hsa_circ_54228,RMVar_hsa_circ_340637,RMVar_hsa_circ_366242,RMVar_hsa_circ_351428,RMVar_hsa_circ_331230,RMVar_hsa_circ_58880 110188 RMVar_ID_110188 Human_SNP_ID_319536760 m1A Human chr7 - 47362997 47362997 47362997 TGGTGATGACCCTGATGATGGTGATGACTGTGATGATGTTGGTGATGGTGATGGTAAATGACTCT TGGTGATGACCCTGATGATGGTGATGACTGTGGTGATGTTGGTGATGGTGATGGTAAATGACTCT T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:47362783..47363201 26863196 MeRIP-seq:(Medium) rs1379855415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842428,Human_RBP_ID_5305868,Human_RBP_ID_23116655,Human_RBP_ID_24236898 RMVar_hsa_circ_37444,RMVar_hsa_circ_54228,RMVar_hsa_circ_340637,RMVar_hsa_circ_366242,RMVar_hsa_circ_351428,RMVar_hsa_circ_331230,RMVar_hsa_circ_58880 110189 RMVar_ID_110189 Human_SNP_ID_319548920 m1A Human chr7 - 47408818 47408818 47408818 TGGCTCCAGGTTGGAAGGGGTGTTATTATACAAACAGATGAAGCATCCCAGGCTTGAGGCACCCA TGGCTCCAGGTTGGAAGGGGTGTTATTATACAGACAGATGAAGCATCCCAGGCTTGAGGCACCCA T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:47408816..47408932 26863196 MeRIP-seq:(Medium) rs544428004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37444,RMVar_hsa_circ_38059,RMVar_hsa_circ_54228,RMVar_hsa_circ_351428,RMVar_hsa_circ_331230,RMVar_hsa_circ_63411,RMVar_hsa_circ_335540,RMVar_hsa_circ_341871,RMVar_hsa_circ_321598,RMVar_hsa_circ_59839,RMVar_hsa_circ_57257,RMVar_hsa_circ_57472 110190 RMVar_ID_110190 Human_SNP_ID_319565413 m1A Human chr7 + 47474481 47474480 47474482 ACACACTGCAACACACACACAACACCTCACACAATACACACAACACAGACATGTACACACACACA ACACACTGCAACACACACACAACACCTCACAC__TACACACAACACAGACATGTACACACACACA CAA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:47474407..47474595 26863196 MeRIP-seq:(Medium) rs1183669692 Functional Loss DEL dbSNP153 33..34 33 - - - 110191 RMVar_ID_110191 Human_SNP_ID_319565414 m1A Human chr7 + 47474481 47474480 47474481 ACACACTGCAACACACACACAACACCTCACACAATACACACAACACAGACATGTACACACACACA ACACACTGCAACACACACACAACACCTCACAC_ATACACACAACACAGACATGTACACACACACA CA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:47474407..47474595 26863196 MeRIP-seq:(Medium) rs1236967673 Functional Loss DEL dbSNP153 33..33 33 - - - 110192 RMVar_ID_110192 Human_SNP_ID_319565471 m1A Human chr7 - 47474614 47474614 47474614 TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGAGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGTGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT T A TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47474580..47475128 26863196 MeRIP-seq:(Medium) rs1308209977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8951800 RMVar_hsa_circ_37444,RMVar_hsa_circ_351428,RMVar_hsa_circ_63411,RMVar_hsa_circ_341871,RMVar_hsa_circ_57257,RMVar_hsa_circ_57472,RMVar_hsa_circ_349290,RMVar_hsa_circ_124921,RMVar_hsa_circ_245087,RMVar_hsa_circ_245088,RMVar_hsa_circ_63766,RMVar_hsa_circ_84433,RMVar_hsa_circ_282851,RMVar_hsa_circ_54084,RMVar_hsa_circ_373210,RMVar_hsa_circ_106174,RMVar_hsa_circ_245096,RMVar_hsa_circ_245098,RMVar_hsa_circ_245099,RMVar_hsa_circ_245097,RMVar_hsa_circ_127348,RMVar_hsa_circ_245100,RMVar_hsa_circ_121399,RMVar_hsa_circ_365251,RMVar_hsa_circ_245102,RMVar_hsa_circ_245103 110193 RMVar_ID_110193 Human_SNP_ID_319565472 m1A Human chr7 - 47474614 47474614 47474614 TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGAGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGGGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47474580..47475128 26863196 MeRIP-seq:(Medium) rs1308209977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8951800 RMVar_hsa_circ_37444,RMVar_hsa_circ_351428,RMVar_hsa_circ_63411,RMVar_hsa_circ_341871,RMVar_hsa_circ_57257,RMVar_hsa_circ_57472,RMVar_hsa_circ_349290,RMVar_hsa_circ_124921,RMVar_hsa_circ_245087,RMVar_hsa_circ_245088,RMVar_hsa_circ_63766,RMVar_hsa_circ_84433,RMVar_hsa_circ_282851,RMVar_hsa_circ_54084,RMVar_hsa_circ_373210,RMVar_hsa_circ_106174,RMVar_hsa_circ_245096,RMVar_hsa_circ_245098,RMVar_hsa_circ_245099,RMVar_hsa_circ_245097,RMVar_hsa_circ_127348,RMVar_hsa_circ_245100,RMVar_hsa_circ_121399,RMVar_hsa_circ_365251,RMVar_hsa_circ_245102,RMVar_hsa_circ_245103 110194 RMVar_ID_110194 Human_SNP_ID_319575557 m1A Human chr7 - 47514481 47514481 47514481 TAAGAAAGATTTGGTAATGGGTTGTTCCACGCAGTTAACCCAACATTATTAAGCACCTGCTAGGA TAAGAAAGATTTGGTAATGGGTTGTTCCACGCGGTTAACCCAACATTATTAAGCACCTGCTAGGA T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47514479..47514655 26863196 MeRIP-seq:(Medium) rs615147 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_15364,GWAS_ID_15365,GWAS_ID_15366,GWAS_ID_15367,GWAS_ID_15368 RMVar_hsa_circ_37444,RMVar_hsa_circ_351428,RMVar_hsa_circ_63411,RMVar_hsa_circ_341871,RMVar_hsa_circ_57472,RMVar_hsa_circ_349290,RMVar_hsa_circ_124921,RMVar_hsa_circ_245087,RMVar_hsa_circ_245088,RMVar_hsa_circ_63766,RMVar_hsa_circ_84433,RMVar_hsa_circ_282851,RMVar_hsa_circ_54084,RMVar_hsa_circ_245098,RMVar_hsa_circ_245099,RMVar_hsa_circ_40186,RMVar_hsa_circ_127348,RMVar_hsa_circ_365251,RMVar_hsa_circ_245102,RMVar_hsa_circ_301011,RMVar_hsa_circ_245105,RMVar_hsa_circ_289564,RMVar_hsa_circ_305905,RMVar_hsa_circ_245106 110195 RMVar_ID_110195 Human_SNP_ID_319575756 m1A Human chr7 - 47515383 47515383 47515383 TGATAGTGATAGTGTAGTTGATGGTGATAGTAACAATGGCAATGGTAACGATTGTGATGATGATG TGATAGTGATAGTGTAGTTGATGGTGATAGTAGCAATGGCAATGGTAACGATTGTGATGATGATG T C TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47515381..47515734 26863196 MeRIP-seq:(Medium) rs779844788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24217776 RMVar_hsa_circ_37444,RMVar_hsa_circ_351428,RMVar_hsa_circ_63411,RMVar_hsa_circ_341871,RMVar_hsa_circ_57472,RMVar_hsa_circ_349290,RMVar_hsa_circ_124921,RMVar_hsa_circ_245087,RMVar_hsa_circ_245088,RMVar_hsa_circ_63766,RMVar_hsa_circ_84433,RMVar_hsa_circ_282851,RMVar_hsa_circ_54084,RMVar_hsa_circ_245098,RMVar_hsa_circ_245099,RMVar_hsa_circ_40186,RMVar_hsa_circ_127348,RMVar_hsa_circ_365251,RMVar_hsa_circ_245102,RMVar_hsa_circ_301011,RMVar_hsa_circ_245105,RMVar_hsa_circ_289564,RMVar_hsa_circ_305905,RMVar_hsa_circ_245106 110196 RMVar_ID_110196 Human_SNP_ID_319592750 m1A Human chr7 + 47581592 47581592 47581592 ACTGCGACATAGCTGCTCCGGTCTCTGCCCTCAGTCCAGGGCGCCCGGGCGCCACGGGTCCCACT ACTGCGACATAGCTGCTCCGGTCTCTGCCCTCGGTCCAGGGCGCCCGGGCGCCACGGGTCCCACT A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:47581576..47581773 26863196 MeRIP-seq:(Medium) rs1038099989 Functional Loss SNV dbSNP153 33..33 33 - - - 110197 RMVar_ID_110197 Human_SNP_ID_319595010 m1A Human chr7 - 47590038 47590038 47590038 AAGAAAGAGAGAGACCATAAGAGAGAAGAGGAAAGAAAAGGAGAAAAAGAGAAGGAGAGGCAGAA AAGAAAGAGAGAGACCATAAGAGAGAAGAGGAGAGAAAAGGAGAAAAAGAGAAGGAGAGGCAGAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:47590011..47590232 26863196 MeRIP-seq:(Medium) rs1562872081 Functional Loss SNV dbSNP153 33..33 33 - - - 110198 RMVar_ID_110198 Human_SNP_ID_319697229 m1A Human chr7 + 47979350 47979350 47979350 GCGGCCTACACCAGCACCCCCATCCCGGCCCCATCCTCCCGCGGCCCCTTCCGGCGCCCATCCCC GCGGCCTACACCAGCACCCCCATCCCGGCCCCCTCCTCCCGCGGCCCCTTCCGGCGCCCATCCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47979340..47979474 26863196 MeRIP-seq:(Medium) rs1250973633 Functional Loss SNV dbSNP153 33..33 33 - - - 110199 RMVar_ID_110199 Human_SNP_ID_320388993 m1A Human chr7 + 50713240 50713240 50713240 TGGAAAGCACGGCTCAGTAAATCTCAGCTGCTATTTTTACTACTGCCACTACTGCCCCTGCCTCC TGGAAAGCACGGCTCAGTAAATCTCAGCTGCTGTTTTTACTACTGCCACTACTGCCCCTGCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:50713238..50713618 26863196 MeRIP-seq:(Medium) rs991212496 Functional Loss SNV dbSNP153 33..33 33 - - - 110200 RMVar_ID_110200 Human_SNP_ID_320389184 m1A Human chr7 + 50713731 50713731 50713731 CCTCCTCCATCCTCACCTCCACCTCCTCTACTATCACATCACCTCCACCTCCTCCACCATCTCTA CCTCCTCCATCCTCACCTCCACCTCCTCTACTGTCACATCACCTCCACCTCCTCCACCATCTCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:50713729..50714077 26863196 MeRIP-seq:(Medium) rs1285547338 Functional Loss SNV dbSNP153 33..33 33 - - - 110201 RMVar_ID_110201 Human_SNP_ID_320397460 m1A Human chr7 + 50746752 50746752 50746752 AGCATCCCCAAACCCCTTCCTGCAGAACACCCATATCACTTCAGGGCCTGCACACCACCCAGTCT AGCATCCCCAAACCCCTTCCTGCAGAACACCCGTATCACTTCAGGGCCTGCACACCACCCAGTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:50746748..50746836 26863196 MeRIP-seq:(Medium) rs1205221169 Functional Loss SNV dbSNP153 33..33 33 - - - 110202 RMVar_ID_110202 Human_SNP_ID_320464983 m1A Human chr7 - 51018248 51018248 51018248 CCATCACCATCACCACCACCACCACCATCGTCACCACCACAGTTACCACCACCATCACCACTGCC CCATCACCATCACCACCACCACCACCATCGTCCCCACCACAGTTACCACCACCATCACCACTGCC T G COBL Ensembl:ENSG00000106078 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51018205..51018288 26863196 MeRIP-seq:(Medium) rs1261347142 Functional Loss SNV dbSNP153 33..33 33 - - - 110203 RMVar_ID_110203 Human_SNP_ID_320502642 m1A Human chr7 + 51169216 51169216 51169216 TCTACTGATAATAATGCTTTCAACAGACTGCCAATCAGAATATGTTTAAATCTACCTATGAGCTG TCTACTGATAATAATGCTTTCAACAGACTGCCCATCAGAATATGTTTAAATCTACCTATGAGCTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51169212..51169295 26863196 MeRIP-seq:(Medium) rs917874845 Functional Loss SNV dbSNP153 33..33 33 - - - 110204 RMVar_ID_110204 Human_SNP_ID_320502643 m1A Human chr7 + 51169216 51169216 51169216 TCTACTGATAATAATGCTTTCAACAGACTGCCAATCAGAATATGTTTAAATCTACCTATGAGCTG TCTACTGATAATAATGCTTTCAACAGACTGCCTATCAGAATATGTTTAAATCTACCTATGAGCTG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51169212..51169295 26863196 MeRIP-seq:(Medium) rs917874845 Functional Loss SNV dbSNP153 33..33 33 - - - 110205 RMVar_ID_110205 Human_SNP_ID_320515345 m1A Human chr7 + 51219926 51219926 51219926 AGAGTGGCAGCCTTTCCAGGAGGTGGGGGAGCACGAGCCTTCATCTTCCTCCTTAAAAACAACAA AGAGTGGCAGCCTTTCCAGGAGGTGGGGGAGCGCGAGCCTTCATCTTCCTCCTTAAAAACAACAA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:51219876..51220029 26863196 MeRIP-seq:(Medium) rs761432047 Functional Loss SNV dbSNP153 33..33 33 - - - 110206 RMVar_ID_110206 Human_SNP_ID_320515351 m1A Human chr7 - 51219937 51219937 51219937 GTGCCTTTGTGTTGTTGTTTTTAAGGAGGAAGATGAAGGCTCGTGCTCCCCCACCTCCTGGAAAG GTGCCTTTGTGTTGTTGTTTTTAAGGAGGAAGTTGAAGGCTCGTGCTCCCCCACCTCCTGGAAAG T A COBL Ensembl:ENSG00000106078 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:51219851..51220008 26863196 MeRIP-seq:(Medium) rs755028559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954435,Human_RBP_ID_4963944,Human_RBP_ID_9404452 Human_Splice_Rec_867536,Human_Splice_Rec_867560,Human_Splice_Rec_867610,Human_Splice_Rec_867624,Human_Splice_Rec_867638,Human_Splice_Rec_867654,Human_Splice_Rec_867668 RMVar_hsa_circ_14327,RMVar_hsa_circ_53550,RMVar_hsa_circ_35426,RMVar_hsa_circ_267597 110207 RMVar_ID_110207 Human_SNP_ID_320515352 m1A Human chr7 - 51219937 51219937 51219937 GTGCCTTTGTGTTGTTGTTTTTAAGGAGGAAGATGAAGGCTCGTGCTCCCCCACCTCCTGGAAAG GTGCCTTTGTGTTGTTGTTTTTAAGGAGGAAGGTGAAGGCTCGTGCTCCCCCACCTCCTGGAAAG T C COBL Ensembl:ENSG00000106078 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:51219851..51220008 26863196 MeRIP-seq:(Medium) rs755028559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954435,Human_RBP_ID_4963944,Human_RBP_ID_9404452 Human_Splice_Rec_867536,Human_Splice_Rec_867560,Human_Splice_Rec_867610,Human_Splice_Rec_867624,Human_Splice_Rec_867638,Human_Splice_Rec_867654,Human_Splice_Rec_867668 RMVar_hsa_circ_14327,RMVar_hsa_circ_53550,RMVar_hsa_circ_35426,RMVar_hsa_circ_267597 110208 RMVar_ID_110208 Human_SNP_ID_320517972 m1A Human chr7 - 51230299 51230299 51230299 AGCCATGACTGAAATGGAGAGGCAGGAGAGGCAGTGGTGCCCCGGAGAGCTCTTCATTGGGTGTT AGCCATGACTGAAATGGAGAGGCAGGAGAGGCGGTGGTGCCCCGGAGAGCTCTTCATTGGGTGTT T C COBL Ensembl:ENSG00000106078 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51230297..51230530 26863196 MeRIP-seq:(Medium) rs547721775 Functional Loss SNV dbSNP153 33..33 33 - - - 110209 RMVar_ID_110209 Human_SNP_ID_320525401 m1A Human chr7 - 51260997 51260997 51260997 GAATGGCTGGAGGTGAAGCAGGAGAGATGGGCAATGGAGAAGGGGTATGGAGGTTTATAAAGTTC GAATGGCTGGAGGTGAAGCAGGAGAGATGGGCGATGGAGAAGGGGTATGGAGGTTTATAAAGTTC T C COBL Ensembl:ENSG00000106078 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51260996..51261141 26863196 MeRIP-seq:(Medium) rs936536618 Functional Loss SNV dbSNP153 33..33 33 - - - 110210 RMVar_ID_110210 Human_SNP_ID_320528748 m1A Human chr7 - 51274115 51274115 51274115 ACAGCTGGCAGCTGCAGGTCCTGTGCTGGGGAAGGGGAGCGAGGGCCTCACTTAAGGCATGGACT ACAGCTGGCAGCTGCAGGTCCTGTGCTGGGGATGGGGAGCGAGGGCCTCACTTAAGGCATGGACT T A COBL Ensembl:ENSG00000106078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:51274112..51274226 26863196 MeRIP-seq:(Medium) rs1426069144 Functional Loss SNV dbSNP153 33..33 33 - - - 110211 RMVar_ID_110211 Human_SNP_ID_320532737 m1A Human chr7 + 51290640 51290636 51290640 GCTTAAGCCTTCCTGGGCTCCCTACTGCCCTGACTTTCTCTCCAGCTTCCCACACAACCTCAGCC GCTTAAGCCTTCCTGGGCTCCCTACTGCC____CTTTCTCTCCAGCTTCCCACACAACCTCAGCC CCTGA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51290637..51290779 26863196 MeRIP-seq:(Medium) rs1326101251 Functional Loss DEL dbSNP153 30..33 33 - - - 110212 RMVar_ID_110212 Human_SNP_ID_320532738 m1A Human chr7 + 51290640 51290640 51290640 GCTTAAGCCTTCCTGGGCTCCCTACTGCCCTGACTTTCTCTCCAGCTTCCCACACAACCTCAGCC GCTTAAGCCTTCCTGGGCTCCCTACTGCCCTGCCTTTCTCTCCAGCTTCCCACACAACCTCAGCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:51290637..51290779 26863196 MeRIP-seq:(Medium) rs1367260931 Functional Loss SNV dbSNP153 33..33 33 - - - 110213 RMVar_ID_110213 Human_SNP_ID_320539284 m1A Human chr7 - 51316633 51316633 51316633 GGAGCACCGCCCGCGTCCCGGCCCCCGGCACCATGGACGCGCCGCGCGCCTCGGCGGCCAAGCCC GGAGCACCGCCCGCGTCCCGGCCCCCGGCACCGTGGACGCGCCGCGCGCCTCGGCGGCCAAGCCC T C COBL Ensembl:ENSG00000106078 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:51316538..51316800 26863196 MeRIP-seq:(Medium) rs1020812315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4963945 Human_Splice_Rec_867535,Human_Splice_Rec_867559,Human_Splice_Rec_867609,Human_Splice_Rec_867623,Human_Splice_Rec_867637,Human_Splice_Rec_867653 110214 RMVar_ID_110214 Human_SNP_ID_320539537 m1A Human chr7 + 51317174 51317174 51317174 AGGGGAACCACCTGGAGCCTGGAGGCCGTGCGAGGGCGAGGTGGGCGGACCAGCCCGGGAGGACT AGGGGAACCACCTGGAGCCTGGAGGCCGTGCGTGGGCGAGGTGGGCGGACCAGCCCGGGAGGACT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:51317074..51317218 26863196 MeRIP-seq:(Medium) rs1418397644 Functional Loss SNV dbSNP153 33..33 33 - - - 110215 RMVar_ID_110215 Human_SNP_ID_321356851 m1A Human chr7 + 54419515 54419515 54419515 GCAGGTGGAGTGGCCGAAGCCATCTCCAAGACAGCGGTAGCGCCCATCGAGCAGGTCAAGCTGCT GCAGGTGGAGTGGCCGAAGCCATCTCCAAGACGGCGGTAGCGCCCATCGAGCAGGTCAAGCTGCT A G LINC01445,SLC25A5P3 Ensembl:ENSG00000231427,Ensembl:ENSG00000213673 lincRNA,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1241688180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27114710 110216 RMVar_ID_110216 Human_SNP_ID_321435820 m1A Human chr7 + 54719439 54719439 54719439 ACTATTTACTCCTTTTCCCACACCTGCTTACTACCTACATCCCACCTTACACTCACTCATTACTT ACTATTTACTCCTTTTCCCACACCTGCTTACTGCCTACATCCCACCTTACACTCACTCATTACTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:54719331..54719507 26863196 MeRIP-seq:(Medium) rs892326323 Functional Loss SNV dbSNP153 33..33 33 - - - 110217 RMVar_ID_110217 Human_SNP_ID_321436695 m1A Human chr7 - 54722528 54722525 54722529 GAGAGGGAGAAGAGAGAGACAGAAAGACAGAGAGACAGACACACAGAGAGAAAGCTGGGGAGAGG GAGAGGGAGAAGAGAGAGACAGAAAGACAGA____CAGACACACAGAGAGAAAGCTGGGGAGAGG GTCTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:54722482..54722568 26863196 MeRIP-seq:(Medium) rs1258652098 Functional Loss DEL dbSNP153 32..35 33 - - - 110218 RMVar_ID_110218 Human_SNP_ID_321436696 m1A Human chr7 - 54722528 54722525 54722529 GAGAGGGAGAAGAGAGAGACAGAAAGACAGAGAGACAGACACACAGAGAGAAAGCTGGGGAGAGG GAGAGGGAGAAGAGAGAGACAGAAAGACAGA__GACAGACACACAGAGAGAAAGCTGGGGAGAGG GTCTC GTC - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:54722482..54722568 26863196 MeRIP-seq:(Medium) rs1258652098 Functional Loss DEL dbSNP153 32..33 33 - - - 110219 RMVar_ID_110219 Human_SNP_ID_321436770 m1A Human chr7 - 54722736 54722735 54722737 GAGAGAGAAAGAGGGAGAGGAGGGAGAGAGAGACAGAGAGAGAAAGGAAGAGAAAGTGAGAGAGA GAGAGAGAAAGAGGGAGAGGAGGGAGAGAGA__CAGAGAGAGAAAGGAAGAGAAAGTGAGAGAGA GTC G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:54722692..54722778 26863196 MeRIP-seq:(Medium) rs1213658141 Functional Loss DEL dbSNP153 32..33 33 - - - 110220 RMVar_ID_110220 Human_SNP_ID_321442564 m1A Human chr7 + 54747292 54747292 54747292 GAATACCCCTTTAACCTATTGCCCTTTACAAAAATCACAGGAGCAGTTTGTCCATACTCCTCAAC GAATACCCCTTTAACCTATTGCCCTTTACAAACATCACAGGAGCAGTTTGTCCATACTCCTCAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:54747250..54747338 26863196 MeRIP-seq:(Medium) rs985530721 Functional Loss SNV dbSNP153 33..33 33 - - - 110221 RMVar_ID_110221 Human_SNP_ID_321445236 m1A Human chr7 + 54757547 54757547 54757547 CATCTTTTAACCAGCCGAATGGAGTCCTTTACAAACTGCCGACTTGGCTCAACAAACTGCATTAC CATCTTTTAACCAGCCGAATGGAGTCCTTTACGAACTGCCGACTTGGCTCAACAAACTGCATTAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:54755801..54759070 26863410 MeRIP-seq:(Medium) rs746317531 Functional Loss SNV dbSNP153 33..33 33 - - - 110222 RMVar_ID_110222 Human_SNP_ID_321445246 m1A Human chr7 + 54757575 54757575 54757575 TTACAAACTGCCGACTTGGCTCAACAAACTGCATTACCTGATCCATGACTGCCTGTTTAAAACAA TTACAAACTGCCGACTTGGCTCAACAAACTGCCTTACCTGATCCATGACTGCCTGTTTAAAACAA A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:54755864..54759070 26863410 MeRIP-seq:(Medium) rs770373802 Functional Loss SNV dbSNP153 33..33 33 - - - 110223 RMVar_ID_110223 Human_SNP_ID_321445248 m1A Human chr7 - 54757581 54757581 54757581 TCTTTTTTGTTTTAAACAGGCAGTCATGGATCAGGTAATGCAGTTTGTTGAGCCAAGTCGGCAGT TCTTTTTTGTTTTAAACAGGCAGTCATGGATCGGGTAATGCAGTTTGTTGAGCCAAGTCGGCAGT T C SEC61G Ensembl:ENSG00000132432 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:54757476..54759225;chr7:54755826..54759225 26863196 MeRIP-seq:(Medium) rs1329082311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14394,Human_RBP_ID_253425,Human_RBP_ID_685878,Human_RBP_ID_793460,Human_RBP_ID_844158,Human_RBP_ID_2044198,Human_RBP_ID_3848590,Human_RBP_ID_4955781,Human_RBP_ID_5327849,Human_RBP_ID_8668829,Human_RBP_ID_8944160,Human_RBP_ID_16177467,Human_RBP_ID_18426002,Human_RBP_ID_22463991,Human_RBP_ID_22531807,Human_RBP_ID_23215503,Human_RBP_ID_24219250 Human_Splice_Rec_868078,Human_Splice_Rec_868079,Human_Splice_Rec_868084,Human_Splice_Rec_868085,Human_Splice_Rec_868092,Human_Splice_Rec_868093,Human_Splice_Rec_868098,Human_Splice_Rec_868099,Human_Splice_Rec_868104,Human_Splice_Rec_868105,Human_Splice_Rec_868108,Human_Splice_Rec_868109 Human_miRNA_ID_2234541,Human_miRNA_ID_2733428,Human_miRNA_ID_2904592,Human_miRNA_ID_3028699 RMVar_hsa_circ_245162,RMVar_hsa_circ_108595,RMVar_hsa_circ_110477,RMVar_hsa_circ_245163,RMVar_hsa_circ_245164 110224 RMVar_ID_110224 Human_SNP_ID_321458855 m1A Human chr7 - 54811960 54811960 54811960 AGGCCATGAGAGCCGGAATTCTCACGAGCAGCAGCGGCCCTGTGGCCCTCAGCAGAGGGACTGAC AGGCCATGAGAGCCGGAATTCTCACGAGCAGCTGCGGCCCTGTGGCCCTCAGCAGAGGGACTGAC T A lnc-SEC61G-1 RNACentral:URS0000D5859B lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:54811876..54812102 26863196 MeRIP-seq:(Medium) rs1453379856 Functional Loss SNV dbSNP153 33..33 33 - - - 110225 RMVar_ID_110225 Human_SNP_ID_321463142 m1A Human chr7 - 54831093 54831093 54831093 GAGTAGGCAAGGGGTGGGAGAAGGTTATTCAGATAGGATGGTCTGGAAAGGTCTCTGTAGAGGTT GAGTAGGCAAGGGGTGGGAGAAGGTTATTCAGTTAGGATGGTCTGGAAAGGTCTCTGTAGAGGTT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:54831045..54831170 26863196 MeRIP-seq:(Medium) rs1172458981 Functional Loss SNV dbSNP153 33..33 33 - - - 110226 RMVar_ID_110226 Human_SNP_ID_321508709 m1A Human chr7 - 55019405 55019405 55019405 GCGGTTGGGCGGGCTGCGGGGTCCGGGGCGCGATCCGGGGGCGGCGCGGGAGCCGGCGAGACACG GCGGTTGGGCGGGCTGCGGGGTCCGGGGCGCGGTCCGGGGGCGGCGCGGGAGCCGGCGAGACACG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:55019394..55019459 26863196 MeRIP-seq:(Medium) rs1426039094 Functional Loss SNV dbSNP153 33..33 33 - - - 110227 RMVar_ID_110227 Human_SNP_ID_321545395 m1A Human chr7 + 55166957 55166957 55166957 GTTGATGGTGGTGATGGTGATGAGGAGGTGGGAGTCACAATGGTGGTGATGAGGGTGGTGATGAT GTTGATGGTGGTGATGGTGATGAGGAGGTGGGGGTCACAATGGTGGTGATGAGGGTGGTGATGAT A G EGFR Ensembl:ENSG00000146648 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:55166953..55167204 26863196 MeRIP-seq:(Medium) rs1317789708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4273,RMVar_hsa_circ_301392,RMVar_hsa_circ_36120,RMVar_hsa_circ_245169,RMVar_hsa_circ_123673,RMVar_hsa_circ_265679,RMVar_hsa_circ_78743,RMVar_hsa_circ_245170,RMVar_hsa_circ_361087,RMVar_hsa_circ_60559,RMVar_hsa_circ_74577,RMVar_hsa_circ_245175,RMVar_hsa_circ_13277,RMVar_hsa_circ_376622,RMVar_hsa_circ_297017,RMVar_hsa_circ_245177 110228 RMVar_ID_110228 Human_SNP_ID_321545590 m1A Human chr7 + 55167434 55167432 55167435 TGGTGGTGGTGATGAGGGTGGTGATGGTGATGAGGAGGTGGGAGTCACAACGTTGGTGGTGATGA TGGTGGTGGTGATGAGGGTGGTGATGGTGAT___GAGGTGGGAGTCACAACGTTGGTGGTGATGA TGAG T EGFR Ensembl:ENSG00000146648 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:55167418..55167543 26863196 MeRIP-seq:(Medium) rs1335838963 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_843322,Human_RBP_ID_3862364,Human_RBP_ID_8218314,Human_RBP_ID_26107357 RMVar_hsa_circ_4273,RMVar_hsa_circ_301392,RMVar_hsa_circ_36120,RMVar_hsa_circ_245169,RMVar_hsa_circ_123673,RMVar_hsa_circ_265679,RMVar_hsa_circ_78743,RMVar_hsa_circ_245170,RMVar_hsa_circ_361087,RMVar_hsa_circ_60559,RMVar_hsa_circ_74577,RMVar_hsa_circ_245175,RMVar_hsa_circ_13277,RMVar_hsa_circ_376622,RMVar_hsa_circ_297017,RMVar_hsa_circ_245177 110229 RMVar_ID_110229 Human_SNP_ID_321545592 m1A Human chr7 + 55167434 55167434 55167434 TGGTGGTGGTGATGAGGGTGGTGATGGTGATGAGGAGGTGGGAGTCACAACGTTGGTGGTGATGA TGGTGGTGGTGATGAGGGTGGTGATGGTGATGGGGAGGTGGGAGTCACAACGTTGGTGGTGATGA A G EGFR Ensembl:ENSG00000146648 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:55167418..55167543 26863196 MeRIP-seq:(Medium) rs1409482768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_843322,Human_RBP_ID_3862364,Human_RBP_ID_8218314,Human_RBP_ID_26107357 RMVar_hsa_circ_4273,RMVar_hsa_circ_301392,RMVar_hsa_circ_36120,RMVar_hsa_circ_245169,RMVar_hsa_circ_123673,RMVar_hsa_circ_265679,RMVar_hsa_circ_78743,RMVar_hsa_circ_245170,RMVar_hsa_circ_361087,RMVar_hsa_circ_60559,RMVar_hsa_circ_74577,RMVar_hsa_circ_245175,RMVar_hsa_circ_13277,RMVar_hsa_circ_376622,RMVar_hsa_circ_297017,RMVar_hsa_circ_245177 110230 RMVar_ID_110230 Human_SNP_ID_321551534 m1A Human chr7 + 55189772 55189772 55189772 ACGAACAAAAGGTACAAATGTGAAGAACGAACAGGGTAGAAAGAAAGGAGAAAGCAAGGGTGAGG ACGAACAAAAGGTACAAATGTGAAGAACGAACGGGGTAGAAAGAAAGGAGAAAGCAAGGGTGAGG A G EGFR Ensembl:ENSG00000146648 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:55189766..55189857 26863196 MeRIP-seq:(Medium) rs551923467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36120,RMVar_hsa_circ_265679,RMVar_hsa_circ_60559,RMVar_hsa_circ_245175,RMVar_hsa_circ_376622,RMVar_hsa_circ_48682,RMVar_hsa_circ_61260,RMVar_hsa_circ_351263,RMVar_hsa_circ_268488 110231 RMVar_ID_110231 Human_SNP_ID_321554581 m1A Human chr7 + 55201252 55201250 55201253 AGACTCCAACTTCTACCGTGCCCTGATGGATGAAGAAGACATGGACGACGTGGTGGATGCCGACG AGACTCCAACTTCTACCGTGCCCTGATGGAT___GAAGACATGGACGACGTGGTGGATGCCGACG TGAA T EGFR Ensembl:ENSG00000146648 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:55201201..55201325 26863196 MeRIP-seq:(Medium) rs760292181 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_84959,Human_RBP_ID_953186,Human_RBP_ID_5622989,Human_RBP_ID_9404453 Human_Splice_Rec_868168,Human_Splice_Rec_868220,Human_Splice_Rec_868300,Human_Splice_Rec_868402 RMVar_hsa_circ_265679,RMVar_hsa_circ_245175,RMVar_hsa_circ_376622,RMVar_hsa_circ_268488 110232 RMVar_ID_110232 Human_SNP_ID_321556236 m1A Human chr7 - 55205377 55205377 55205377 ACAGTGTTGAGATACTCGGGGTTGCCCACTGCAGTGCTGTGGGGGTCCTGGTAGTGTGGGTCTCT ACAGTGTTGAGATACTCGGGGTTGCCCACTGCCGTGCTGTGGGGGTCCTGGTAGTGTGGGTCTCT T G EGFR-AS1 RNACentral:URS00009AF7DE lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:55205326..55205400 26863196 MeRIP-seq:(Medium) rs768310160 Functional Loss SNV dbSNP153 33..33 33 - - - 110233 RMVar_ID_110233 Human_SNP_ID_321556353 m1A Human chr7 + 55205677 55205677 55205677 ATCCAGACTCTTTCGATACCCAGGACCAAGCCACAGCAGGTCCTCCATCCCAACAGCCATGCCCG ATCCAGACTCTTTCGATACCCAGGACCAAGCCCCAGCAGGTCCTCCATCCCAACAGCCATGCCCG A C EGFR Ensembl:ENSG00000146648 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:55205626..55205700 26863196 MeRIP-seq:(Medium) rs1260041771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18883889 RMVar_hsa_circ_265679 110234 RMVar_ID_110234 Human_SNP_ID_321595217 m1A Human chr7 + 55365731 55365731 55365731 GGGCCACGGGGAAGGTGCGAGGAGGCGCGAGCAGGCTGTGAGCCGCTGGGCGCTCCCGCGAGCCC GGGCCACGGGGAAGGTGCGAGGAGGCGCGAGCCGGCTGTGAGCCGCTGGGCGCTCCCGCGAGCCC A C LANCL2 Ensembl:ENSG00000132434 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:55365680..55365765 26863196 MeRIP-seq:(Medium) rs1562853276 Functional Loss SNV dbSNP153 33..33 33 - - - 110235 RMVar_ID_110235 Human_SNP_ID_321647215 m1A Human chr7 - 55571728 55571728 55571728 TGAGCAGCGGGAGGAGGCGTTCCCGCGTGTGAAAATGAAGTGCAGCCTTTAGGTGCGGGGAGGAA TGAGCAGCGGGAGGAGGCGTTCCCGCGTGTGAGAATGAAGTGCAGCCTTTAGGTGCGGGGAGGAA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:55571702..55571806 26863196 MeRIP-seq:(Medium) rs966573728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3860558,Human_RBP_ID_5328450 Human_Splice_Rec_868495 RMVar_hsa_circ_116365,RMVar_hsa_circ_125741,RMVar_hsa_circ_245185,RMVar_hsa_circ_245184 110236 RMVar_ID_110236 Human_SNP_ID_321689514 m1A Human chr7 - 55743551 55743551 55743551 GCCCCTCCCACGCTGACCCCTTGCCTCACACCAGCCCCTCCCATGCTGACCCCTTGCCTCACACG GCCCCTCCCACGCTGACCCCTTGCCTCACACCGGCCCCTCCCATGCTGACCCCTTGCCTCACACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:55743500..55743592 26863196 MeRIP-seq:(Medium) rs558962637 Functional Loss SNV dbSNP153 33..33 33 - - - 110237 RMVar_ID_110237 Human_SNP_ID_321689515 m1A Human chr7 - 55743551 55743551 55743551 GCCCCTCCCACGCTGACCCCTTGCCTCACACCAGCCCCTCCCATGCTGACCCCTTGCCTCACACG GCCCCTCCCACGCTGACCCCTTGCCTCACACCCGCCCCTCCCATGCTGACCCCTTGCCTCACACG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:55743500..55743592 26863196 MeRIP-seq:(Medium) rs558962637 Functional Loss SNV dbSNP153 33..33 33 - - - 110238 RMVar_ID_110238 Human_SNP_ID_321725478 m1A Human chr7 - 55887539 55887538 55887539 GGCCCCGCAGCCTGAGCCAATGACGCCCGGTGACTGGGCTCCTGGGGCCGGTCCAGCCACCGGCG GGCCCCGCAGCCTGAGCCAATGACGCCCGGTG_CTGGGCTCCTGGGGCCGGTCCAGCCACCGGCG GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:55887488..55887623 26863196 MeRIP-seq:(Medium) rs1238399789 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18451750 110239 RMVar_ID_110239 Human_SNP_ID_321725479 m1A Human chr7 - 55887539 55887539 55887539 GGCCCCGCAGCCTGAGCCAATGACGCCCGGTGACTGGGCTCCTGGGGCCGGTCCAGCCACCGGCG GGCCCCGCAGCCTGAGCCAATGACGCCCGGTGGCTGGGCTCCTGGGGCCGGTCCAGCCACCGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:55887488..55887623 26863196 MeRIP-seq:(Medium) rs1379812852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18451750 110240 RMVar_ID_110240 Human_SNP_ID_321725484 m1A Human chr7 + 55887559 55887559 55887559 CCAGGAGCCCAGTCACCGGGCGTCATTGGCTCAGGCTGCGGGGCCCTCGGCACCTTCTCCCTCCC CCAGGAGCCCAGTCACCGGGCGTCATTGGCTCCGGCTGCGGGGCCCTCGGCACCTTCTCCCTCCC A C AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:55887517..55887677 26863196 MeRIP-seq:(Medium) rs1358014753 Functional Loss SNV dbSNP153 33..33 33 - - - 110241 RMVar_ID_110241 Human_SNP_ID_321726173 m1A Human chr7 + 55887913 55887912 55887913 GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCAGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGC_GGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG CA C AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr7:55887799..55887929;chr7:55887790..55887979 26863196 MeRIP-seq:(Medium) rs1250550613 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8218317 110242 RMVar_ID_110242 Human_SNP_ID_321726174 m1A Human chr7 + 55887913 55887913 55887913 GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCAGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCCGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG A C AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr7:55887799..55887929;chr7:55887790..55887979 26863196 MeRIP-seq:(Medium) rs1438807942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8218317 110243 RMVar_ID_110243 Human_SNP_ID_321726175 m1A Human chr7 + 55887913 55887913 55887913 GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCAGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCGGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr7:55887799..55887929;chr7:55887790..55887979 26863196 MeRIP-seq:(Medium) rs1438807942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8218317 110244 RMVar_ID_110244 Human_SNP_ID_321726176 m1A Human chr7 + 55887913 55887913 55887913 GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCAGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG GGCGGCGGGCGGCGGCGGCGGCGGGAGGCGGCTGGTGGCGGGAGGGGCGGCCGCTGTCCCCGCTG A T AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr7:55887799..55887929;chr7:55887790..55887979 26863196 MeRIP-seq:(Medium) rs1438807942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8218317 110245 RMVar_ID_110245 Human_SNP_ID_321733383 m1A Human chr7 + 55915638 55915638 55915638 CTACGAAAAGTAAGTGGAAAAGAGCATTTTGGACATGTGCTAAAAATCATCTGCAAAAATCACGG CTACGAAAAGTAAGTGGAAAAGAGCATTTTGGGCATGTGCTAAAAATCATCTGCAAAAATCACGG A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:55915522..55915649 26863196 MeRIP-seq:(Medium) rs1016232477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245193,RMVar_hsa_circ_308887,RMVar_hsa_circ_345442 110246 RMVar_ID_110246 Human_SNP_ID_321746073 m1A Human chr7 - 55964703 55964703 55964703 CCCGGCACCTCCCGGGAAGGGCGGCGCTGCTCACCGGAGCCTGGGCAGGAGGCTGCAGGGGGCCG CCCGGCACCTCCCGGGAAGGGCGGCGCTGCTCCCCGGAGCCTGGGCAGGAGGCTGCAGGGGGCCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:55964690..55965099 32194978 MeRIP-seq:(Medium) rs1313324302 Functional Loss SNV dbSNP153 33..33 33 - - - 110247 RMVar_ID_110247 Human_SNP_ID_321749747 m1A Human chr7 + 55978201 55978201 55978201 CTAAAATCCTTATTTGTCCGGAAAGTTGATCCAAGAAAAGATGCCCACTCCAATCTCCTAGCCAA CTAAAATCCTTATTTGTCCGGAAAGTTGATCCGAGAAAAGATGCCCACTCCAATCTCCTAGCCAA A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:55978151..55978200 26863196 MeRIP-seq:(Medium) rs768965920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2044304,Human_RBP_ID_4945115,Human_RBP_ID_18883989,Human_RBP_ID_24219685 Human_Splice_Rec_868728,Human_Splice_Rec_868729,Human_Splice_Rec_868740,Human_Splice_Rec_868741,Human_Splice_Rec_868754,Human_Splice_Rec_868755,Human_Splice_Rec_868772,Human_Splice_Rec_868773,Human_Splice_Rec_868776,Human_Splice_Rec_868777,Human_Splice_Rec_868788,Human_Splice_Rec_868789,Human_Splice_Rec_868802,Human_Splice_Rec_868803,Human_Splice_Rec_868810,Human_Splice_Rec_868811 RMVar_hsa_circ_68642,RMVar_hsa_circ_123218,RMVar_hsa_circ_336552,RMVar_hsa_circ_362054,RMVar_hsa_circ_245197,RMVar_hsa_circ_346772,RMVar_hsa_circ_305234,RMVar_hsa_circ_245199,RMVar_hsa_circ_245200,RMVar_hsa_circ_245198 110248 RMVar_ID_110248 Human_SNP_ID_321762875 m1A Human chr7 - 56025907 56025907 56025907 GCAGCATTTGAAATGGTGTAGAGGAATAAAAAAACACATGACATAGGCCGGGTGCGGTGGCTCAT GCAGCATTTGAAATGGTGTAGAGGAATAAAAACACACATGACATAGGCCGGGTGCGGTGGCTCAT T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:56025903..56026023 26863196 MeRIP-seq:(Medium) rs942993839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22731138 RMVar_hsa_circ_5270,RMVar_hsa_circ_24061 110249 RMVar_ID_110249 Human_SNP_ID_321769458 m1A Human chr7 - 56051320 56051320 56051320 GTGCTGTGAGGCCTAGCGAAGATGAAGATAGAATGCAAGGTAGAAAGTGCTGGATACCTTTAGAA GTGCTGTGAGGCCTAGCGAAGATGAAGATAGAGTGCAAGGTAGAAAGTGCTGGATACCTTTAGAA T C PSPH Ensembl:ENSG00000146733 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56051270..56051397 26863196 MeRIP-seq:(Medium) rs1319792440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2044354,Human_RBP_ID_4945215,Human_RBP_ID_16180246,Human_RBP_ID_24219783 Human_Splice_Rec_868919,Human_Splice_Rec_868931 110250 RMVar_ID_110250 Human_SNP_ID_321769653 m1A Human chr7 - 56051807 56051807 56051807 AGCGGAGGAAAAGGAAACGATGCTGAGTGCCCAGAGCCGGCGCGGCGTGGCCGGGAGGAACTATC AGCGGAGGAAAAGGAAACGATGCTGAGTGCCCGGAGCCGGCGCGGCGTGGCCGGGAGGAACTATC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:56051776..56051825 26863196 MeRIP-seq:(Medium) rs1218901952 Functional Loss SNV dbSNP153 33..33 33 - - - 110251 RMVar_ID_110251 Human_SNP_ID_321769705 m1A Human chr7 - 56051868 56051868 56051868 CCTGCGCTCGGGCCACCTCGGCCTTGGGGTTCAGGGTCTTCACCGCCGCCATAGCTGCTCCAGCG CCTGCGCTCGGGCCACCTCGGCCTTGGGGTTCTGGGTCTTCACCGCCGCCATAGCTGCTCCAGCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56051751..56052027 26863196 MeRIP-seq:(Medium) rs1452184307 Functional Loss SNV dbSNP153 33..33 33 - - - 110252 RMVar_ID_110252 Human_SNP_ID_321769884 m1A Human chr7 - 56052377 56052377 56052377 CAGAAATGAACCAGACTATGACTTTTTCAACGATAACTAAAAGTCCCATTAGAAAACGGGCTTTT CAGAAATGAACCAGACTATGACTTTTTCAACGGTAACTAAAAGTCCCATTAGAAAACGGGCTTTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56052374..56052517 26863196 MeRIP-seq:(Medium) rs374041027 Functional Loss SNV dbSNP153 33..33 33 - - - 110253 RMVar_ID_110253 Human_SNP_ID_321769902 m1A Human chr7 + 56052403 56052403 56052403 TAGTTATCGTTGAAAAAGTCATAGTCTGGTTCATTTCTGTCCTTTAAACAGGCTCGTTTCTGGCG TAGTTATCGTTGAAAAAGTCATAGTCTGGTTCCTTTCTGTCCTTTAAACAGGCTCGTTTCTGGCG A C CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:56052401..56052425 26863196 MeRIP-seq:(Medium) rs1401960523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22011829,Human_RBP_ID_22554711,Human_RBP_ID_26107773 Human_Splice_Rec_868951,Human_Splice_Rec_868975 RMVar_hsa_circ_102641,RMVar_hsa_circ_245222 110254 RMVar_ID_110254 Human_SNP_ID_321770522 m1A Human chr7 - 56054354 56054353 56054354 TGTTGGGTGTTGAATTTGCTGTAAGTAGAAAAAGAATGAATCACTTAAAACAATATGAAGCAGTC TGTTGGGTGTTGAATTTGCTGTAAGTAGAAAA_GAATGAATCACTTAAAACAATATGAAGCAGTC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:56054351..56054400 26863196 MeRIP-seq:(Medium) rs1346471024 Functional Loss DEL dbSNP153 33..33 33 - - - 110255 RMVar_ID_110255 Human_SNP_ID_321770523 m1A Human chr7 - 56054354 56054354 56054354 TGTTGGGTGTTGAATTTGCTGTAAGTAGAAAAAGAATGAATCACTTAAAACAATATGAAGCAGTC TGTTGGGTGTTGAATTTGCTGTAAGTAGAAAAGGAATGAATCACTTAAAACAATATGAAGCAGTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:56054351..56054400 26863196 MeRIP-seq:(Medium) rs1225733463 Functional Loss SNV dbSNP153 33..33 33 - - - 110256 RMVar_ID_110256 Human_SNP_ID_321773358 m1A Human chr7 + 56063667 56063667 56063667 AAGAGGAGTCAACTAGAGGCAAGGGAGTTGAGAGAGCTGCAACTGTAAAGGGCAAGAACAGGCAG AAGAGGAGTCAACTAGAGGCAAGGGAGTTGAGGGAGCTGCAACTGTAAAGGGCAAGAACAGGCAG A G CCT6A Ensembl:ENSG00000146731 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:56063616..56063741 26863196 MeRIP-seq:(Medium) rs1328897278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84985,Human_RBP_ID_7746665,Human_RBP_ID_8220084,Human_RBP_ID_16180625,Human_RBP_ID_24219837,Human_RBP_ID_26547786 Human_miRNA_ID_1490835,Human_miRNA_ID_1530523,Human_miRNA_ID_2012262,Human_miRNA_ID_2758634,Human_miRNA_ID_2922237 RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_245226,RMVar_hsa_circ_117216,RMVar_hsa_circ_82627,RMVar_hsa_circ_245228,RMVar_hsa_circ_113470,RMVar_hsa_circ_99911,RMVar_hsa_circ_245230,RMVar_hsa_circ_96148,RMVar_hsa_circ_245231,RMVar_hsa_circ_245232 110257 RMVar_ID_110257 Human_SNP_ID_321773363 m1A Human chr7 + 56063676 56063676 56063676 CAACTAGAGGCAAGGGAGTTGAGAGAGCTGCAACTGTAAAGGGCAAGAACAGGCAGAGGTAAAAA CAACTAGAGGCAAGGGAGTTGAGAGAGCTGCAGCTGTAAAGGGCAAGAACAGGCAGAGGTAAAAA A G CCT6A Ensembl:ENSG00000146731 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:56063626..56063732 26863196 MeRIP-seq:(Medium) rs1174337265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_84985,Human_RBP_ID_686196,Human_RBP_ID_7746665,Human_RBP_ID_8220084,Human_RBP_ID_16180625,Human_RBP_ID_24219838,Human_RBP_ID_26547786 Human_miRNA_ID_1490835,Human_miRNA_ID_1804934,Human_miRNA_ID_2012262,Human_miRNA_ID_2758634,Human_miRNA_ID_2922237 RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_245226,RMVar_hsa_circ_117216,RMVar_hsa_circ_82627,RMVar_hsa_circ_245228,RMVar_hsa_circ_113470,RMVar_hsa_circ_99911,RMVar_hsa_circ_245230,RMVar_hsa_circ_96148,RMVar_hsa_circ_245231,RMVar_hsa_circ_245232 110258 RMVar_ID_110258 Human_SNP_ID_321773693 m1A Human chr7 - 56064337 56064337 56064337 GCCACGCGCCGACCAGGAGCGACAGCAGGGGCAGCAGCGGTAACCCATGCCGGGCCATCAGGACT GCCACGCGCCGACCAGGAGCGACAGCAGGGGCCGCAGCGGTAACCCATGCCGGGCCATCAGGACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:56064251..56068650;chr7:56064276..56068675;chr7:56064251..56064417 26863196 MeRIP-seq:(Medium) rs1345083574 Functional Loss SNV dbSNP153 33..33 33 - - - 110259 RMVar_ID_110259 Human_SNP_ID_321773724 m1A Human chr7 - 56064366 56064366 56064366 TGGACGGCCGGTTCACTGACCTAGCTTGAGCCACGCGCCGACCAGGAGCGACAGCAGGGGCAGCA TGGACGGCCGGTTCACTGACCTAGCTTGAGCCCCGCGCCGACCAGGAGCGACAGCAGGGGCAGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56064251..56064420 26863196 MeRIP-seq:(Medium) rs1364757700 Functional Loss SNV dbSNP153 33..33 33 - - - 110260 RMVar_ID_110260 Human_SNP_ID_321774828 m1A Human chr7 - 56068392 56068392 56068392 ATATTTGGATCATATGCAATACTCATGATGGTATAACAAAACACAACAAAAAATGTGGAGGCTTA ATATTTGGATCATATGCAATACTCATGATGGTGTAACAAAACACAACAAAAAATGTGGAGGCTTA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:56068390..56068625 26863196 MeRIP-seq:(Medium) rs1205470141 Functional Loss SNV dbSNP153 33..33 33 - - - 110261 RMVar_ID_110261 Human_SNP_ID_321774839 m1A Human chr7 + 56068429 56068429 56068429 TCATGAGTATTGCATATGATCCAAATATTACCACTTGTTTTATATATATGCATGTATTACTGGTA TCATGAGTATTGCATATGATCCAAATATTACCGCTTGTTTTATATATATGCATGTATTACTGGTA A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56068427..56068606 26863196 MeRIP-seq:(Medium) rs1020926074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233 110262 RMVar_ID_110262 Human_SNP_ID_321780047 m1A Human chr7 - 56087037 56087037 56087037 TGGGCTCCCCTGCTACTTGAGACAAGCTAGCCATTTCCATTTCAGTACAGCTGAAGGACACTTAT TGGGCTCCCCTGCTACTTGAGACAAGCTAGCCGTTTCCATTTCAGTACAGCTGAAGGACACTTAT T C PHKG1 Ensembl:ENSG00000164776 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:56086988..56087106 26863196 MeRIP-seq:(Medium) rs776492837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_869309,Human_Splice_Rec_869345,Human_Splice_Rec_869393 RMVar_hsa_circ_36511 110263 RMVar_ID_110263 Human_SNP_ID_321780048 m1A Human chr7 - 56087037 56087037 56087037 TGGGCTCCCCTGCTACTTGAGACAAGCTAGCCATTTCCATTTCAGTACAGCTGAAGGACACTTAT TGGGCTCCCCTGCTACTTGAGACAAGCTAGCCCTTTCCATTTCAGTACAGCTGAAGGACACTTAT T G PHKG1 Ensembl:ENSG00000164776 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:56086988..56087106 26863196 MeRIP-seq:(Medium) rs776492837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_869309,Human_Splice_Rec_869345,Human_Splice_Rec_869393 RMVar_hsa_circ_36511 110264 RMVar_ID_110264 Human_SNP_ID_321784652 m1A Human chr7 - 56102977 56102974 56102977 GCCTCAGGGAACCCAGCCAGCACAGCAGCAGCAGCCTTGCCTCTATGAGATCAAACAGTTTCTGG GCCTCAGGGAACCCAGCCAGCACAGCAGCAGC___CTTGCCTCTATGAGATCAAACAGTTTCTGG GGCT G CHCHD2 Ensembl:ENSG00000106153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56102915..56103050 26863196 MeRIP-seq:(Medium) rs748437721 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_686258,Human_RBP_ID_793029,Human_RBP_ID_843255,Human_RBP_ID_1052582,Human_RBP_ID_3848917,Human_RBP_ID_7746747,Human_RBP_ID_8669217,Human_RBP_ID_18884051,Human_RBP_ID_22463104,Human_RBP_ID_22774895 Human_Splice_Rec_869406,Human_Splice_Rec_869412 Human_miRNA_ID_2534268,Human_miRNA_ID_2536001,Human_miRNA_ID_2647518 RMVar_hsa_circ_113334,RMVar_hsa_circ_79608,RMVar_hsa_circ_89156,RMVar_hsa_circ_245248,RMVar_hsa_circ_245249,RMVar_hsa_circ_245247,RMVar_hsa_circ_245251,RMVar_hsa_circ_82676,RMVar_hsa_circ_371454,RMVar_hsa_circ_245250 110265 RMVar_ID_110265 Human_SNP_ID_321785115 m1A Human chr7 - 56104477 56104477 56104477 TGGGAACTTGATGTTTTTTTCTTTTCTTTCACAGCCGGGCCCCTCAGATGAGAGCTGCACCCAGG TGGGAACTTGATGTTTTTTTCTTTTCTTTCACTGCCGGGCCCCTCAGATGAGAGCTGCACCCAGG T A CHCHD2 Ensembl:ENSG00000106153 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:56104451..56104500;chr7:56104226..56106500;chr7:56104376..56104500 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) rs1192166202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79608,RMVar_hsa_circ_245249 110266 RMVar_ID_110266 Human_SNP_ID_321785663 m1A Human chr7 + 56106313 56106313 56106313 CCGCCCGCGGCCTCCCTCTGCGTCATTGCCCCAGTAGAGTCCGGACGGCCGCGCTTTGGTCTCAA CCGCCCGCGGCCTCCCTCTGCGTCATTGCCCCCGTAGAGTCCGGACGGCCGCGCTTTGGTCTCAA A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:56106309..56106401 26863410 MeRIP-seq:(Medium) rs1248818354 Functional Loss SNV dbSNP153 33..33 33 - - - 110267 RMVar_ID_110267 Human_SNP_ID_321785706 m1A Human chr7 - 56106389 56106389 56106389 TACCTAGGATGCCGCGTGGAAGCCGAAGCCGCACCTCCCGCATGGCCCCTCCGGCCAGGTGAGAC TACCTAGGATGCCGCGTGGAAGCCGAAGCCGCCCCTCCCGCATGGCCCCTCCGGCCAGGTGAGAC T G CHCHD2 Ensembl:ENSG00000106153 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs766155505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686264,Human_RBP_ID_793032,Human_RBP_ID_843979,Human_RBP_ID_1687779,Human_RBP_ID_4945418,Human_RBP_ID_5327855,Human_RBP_ID_9337159,Human_RBP_ID_17665312,Human_RBP_ID_22463531,Human_RBP_ID_27114980,Human_RBP_ID_27358745 Human_Splice_Rec_869403,Human_Splice_Rec_869409 Human_miRNA_ID_2389937,Human_miRNA_ID_2591166 RMVar_hsa_circ_79608,RMVar_hsa_circ_245249 110268 RMVar_ID_110268 Human_SNP_ID_321785712 m1A Human chr7 - 56106401 56106401 56106401 CTAGCCGTCGCTTACCTAGGATGCCGCGTGGAAGCCGAAGCCGCACCTCCCGCATGGCCCCTCCG CTAGCCGTCGCTTACCTAGGATGCCGCGTGGAGGCCGAAGCCGCACCTCCCGCATGGCCCCTCCG T C CHCHD2 Ensembl:ENSG00000106153 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs752705344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686264,Human_RBP_ID_793032,Human_RBP_ID_843979,Human_RBP_ID_1687779,Human_RBP_ID_4945418,Human_RBP_ID_5327855,Human_RBP_ID_5429652,Human_RBP_ID_9211952,Human_RBP_ID_9337159,Human_RBP_ID_22463531,Human_RBP_ID_24219881,Human_RBP_ID_27114980,Human_RBP_ID_27358745 Human_Splice_Rec_869403,Human_Splice_Rec_869409 RMVar_hsa_circ_79608,RMVar_hsa_circ_245249 110269 RMVar_ID_110269 Human_SNP_ID_321834935 m1A Human chr7 + 56291386 56291386 56291386 CAAGCGCTTCAGCAGCCTGATGCTAAAGTTTTAAAAAATTACTTAAAGGTGTTCTTCCAGAGAGC CAAGCGCTTCAGCAGCCTGATGCTAAAGTTTTTAAAAATTACTTAAAGGTGTTCTTCCAGAGAGC A T AC073136.1 Ensembl:ENSG00000223559 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879186527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7779009,Human_RBP_ID_17587020 110270 RMVar_ID_110270 Human_SNP_ID_800020830 m1A Human chr1 + 6601955 6601955 6601955 CACAGTCCTGGTCGCAGCCGCCCACGAGCACGAGGATCTCGGCGAGACCGGTGGACGGGCGAGGA CACAGTCCTGGTCGCAGCCGCCCACGAGCACGCGGATCTCGGCGAGACCGGTGGACGGGCGAGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6599771..6602050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate 110271 RMVar_ID_110271 Human_SNP_ID_800024044 m1A Human chr1 + 7962840 7962840 7962840 TCATCCTGGCTAAAGGAGCAGAGGAAATGGAGACGGTCATCCCTGTAGATGTCATGAGGCGAGCT TCATCCTGGCTAAAGGAGCAGAGGAAATGGAGGCGGTCATCCCTGTAGATGTCATGAGGCGAGCT A G PARK7 Ensembl:ENSG00000116288 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:7962717..7965479 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_18083,Human_RBP_ID_363138,Human_RBP_ID_741881,Human_RBP_ID_803681,Human_RBP_ID_979943,Human_RBP_ID_1435512,Human_RBP_ID_1754622,Human_RBP_ID_4073498,Human_RBP_ID_5312299,Human_RBP_ID_5545001,Human_RBP_ID_5867628,Human_RBP_ID_8319684,Human_RBP_ID_8975429,Human_RBP_ID_9355423,Human_RBP_ID_11116648,Human_RBP_ID_22428974,Human_RBP_ID_23205655,Human_RBP_ID_26797569 Human_Splice_Rec_13730,Human_Splice_Rec_13731,Human_Splice_Rec_13742,Human_Splice_Rec_13743,Human_Splice_Rec_13752,Human_Splice_Rec_13753,Human_Splice_Rec_13764,Human_Splice_Rec_13765,Human_Splice_Rec_13774,Human_Splice_Rec_13775,Human_Splice_Rec_13786,Human_Splice_Rec_13787,Human_Splice_Rec_13794,Human_Splice_Rec_13795,Human_Splice_Rec_13806,Human_Splice_Rec_13807,Human_Splice_Rec_13817 Human_miRNA_ID_2046276,Human_miRNA_ID_2720941 RMVar_hsa_circ_73034,RMVar_hsa_circ_122172,RMVar_hsa_circ_364026,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_32291 110272 RMVar_ID_110272 Human_SNP_ID_800038824 m1A Human chr1 - 37540690 37540690 37540690 GATCGGCAGCACAGGGAACCATCAGAACAGGAACACAGGAGAGCTAGGAACAGTGACCGGGACAG GATCGGCAGCACAGGGAACCATCAGAACAGGAGCACAGGAGAGCTAGGAACAGTGACCGGGACAG T C SNIP1 Ensembl:ENSG00000163877 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:37540278..37540776 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_5819967,Human_RBP_ID_10970340,Human_RBP_ID_26310893 Human_Splice_Rec_48598,Human_Splice_Rec_48606 110273 RMVar_ID_110273 Human_SNP_ID_800041766 m1A Human chr1 - 120029989 120029989 120029989 CTTACTTCTAATGTGCATTTGTTTTTATTTTTAGCATTGCAGTGTCGAGATGGCTATGAACCCTG CTTACTTCTAATGTGCATTTGTTTTTATTTTTGGCATTGCAGTGTCGAGATGGCTATGAACCCTG T C NOTCH2 Ensembl:ENSG00000134250 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:120029967..120030043;chr1:120029971..120030058 26863196 MeRIP-seq:(Medium) rs1553210735 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_Splice_Rec_115713,Human_Splice_Rec_115829,Human_Splice_Rec_115859,Human_Splice_Rec_115867,Human_Splice_Rec_115875,Human_Splice_Rec_115879,Human_Splice_Rec_115885 RMVar_hsa_circ_341993,RMVar_hsa_circ_298274 110274 RMVar_ID_110274 Human_SNP_ID_800046150 m1A Human chr1 - 109282009 109282009 109282009 ACAGTGTTGGTGACTCCAGAGAAACCACTTCGACGGGGCCTCTCCCACCGAAGTGACCCAAATGC ACAGTGTTGGTGACTCCAGAGAAACCACTTCGCCGGGGCCTCTCCCACCGAAGTGACCCAAATGC T G PSRC1 Ensembl:ENSG00000134222 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109281715..109282104 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 6 head and neck Human_RBP_ID_856891,Human_RBP_ID_1407652,Human_RBP_ID_5108687,Human_RBP_ID_9319056,Human_RBP_ID_9356632,Human_RBP_ID_18965765,Human_RBP_ID_26309787 Human_Splice_Rec_105690,Human_Splice_Rec_105704,Human_Splice_Rec_105718,Human_Splice_Rec_105732,Human_Splice_Rec_105746,Human_Splice_Rec_105766,Human_Splice_Rec_105784,Human_Splice_Rec_105792,Human_Splice_Rec_105800,Human_Splice_Rec_105804 RMVar_hsa_circ_21067,RMVar_hsa_circ_8131,RMVar_hsa_circ_347476,RMVar_hsa_circ_39573,RMVar_hsa_circ_135170,RMVar_hsa_circ_3681 110275 RMVar_ID_110275 Human_SNP_ID_800049081 m1A Human chr1 - 212857999 212857999 212857999 GAGGCGGCCCCGCGGGTTGTGTTGCTGGAAAAAGGGGTCTCGATCCAGACCCCAAGAGAGGGTTC GAGGCGGCCCCGCGGGTTGTGTTGCTGGAAAAGGGGGTCTCGATCCAGACCCCAAGAGAGGGTTC T C FLVCR1-DT Ensembl:ENSG00000198468 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:212857948..212858075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_801344 110276 RMVar_ID_110276 Human_SNP_ID_800051453 m1A Human chr1 - 236585212 236585212 236585212 TGGTAATAGAGTGTGTTTATTTTTCAAGGTGGAGGATTTAATAAGCGTGGGTGAGGAGGAGTCCT TGGTAATAGAGTGTGTTTATTTTTCAAGGTGGTGGATTTAATAAGCGTGGGTGAGGAGGAGTCCT T A HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:236585176..236585880 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_Splice_Rec_203284,Human_Splice_Rec_203372 RMVar_hsa_circ_123102,RMVar_hsa_circ_140842,RMVar_hsa_circ_64336,RMVar_hsa_circ_27638,RMVar_hsa_circ_53000,RMVar_hsa_circ_332732,RMVar_hsa_circ_125877,RMVar_hsa_circ_140849,RMVar_hsa_circ_140850,RMVar_hsa_circ_94604,RMVar_hsa_circ_140855,RMVar_hsa_circ_46159,RMVar_hsa_circ_276754,RMVar_hsa_circ_323855,RMVar_hsa_circ_140857,RMVar_hsa_circ_27432,RMVar_hsa_circ_270574,RMVar_hsa_circ_98421,RMVar_hsa_circ_140858,RMVar_hsa_circ_340162,RMVar_hsa_circ_82423,RMVar_hsa_circ_140859,RMVar_hsa_circ_140860 110277 RMVar_ID_110277 Human_SNP_ID_800056863 m1A Human chr1 + 155133751 155133751 155133751 TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGACAATCCACAGGAGAAGAGACTTGCAGCAGGTG TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGGCAATCCACAGGAGAAGAGACTTGCAGCAGGTG A G EFNA1 Ensembl:ENSG00000169242 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_327815,Human_RBP_ID_851790,Human_RBP_ID_5536581,Human_RBP_ID_18969027,Human_RBP_ID_19035473,Human_RBP_ID_22634390,Human_RBP_ID_22751229,Human_RBP_ID_24556231,Human_RBP_ID_26774559 Human_Splice_Rec_136692,Human_Splice_Rec_136693,Human_Splice_Rec_136700,Human_Splice_Rec_136701,Human_Splice_Rec_136707,Human_Splice_Rec_136714,Human_Splice_Rec_136715,Human_Splice_Rec_136720,Human_Splice_Rec_136721 RMVar_hsa_circ_59688 110278 RMVar_ID_110278 Human_SNP_ID_800056875 m1A Human chr1 + 155133751 155133751 155133751 TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGACAATCCACAGGAGAAGAGACTTGCAGCAGGTG TTGTCTTTCAGCTCACAGTCCTCAGGCCCATGTCAATCCACAGGAGAAGAGACTTGCAGCAGGTG A T EFNA1 Ensembl:ENSG00000169242 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4745 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,skin basal_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 10 skin,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_327815,Human_RBP_ID_851790,Human_RBP_ID_5536581,Human_RBP_ID_18969027,Human_RBP_ID_19035473,Human_RBP_ID_22634390,Human_RBP_ID_22751229,Human_RBP_ID_24556231,Human_RBP_ID_26774559 Human_Splice_Rec_136692,Human_Splice_Rec_136693,Human_Splice_Rec_136700,Human_Splice_Rec_136701,Human_Splice_Rec_136707,Human_Splice_Rec_136714,Human_Splice_Rec_136715,Human_Splice_Rec_136720,Human_Splice_Rec_136721 GWAS_ID_12205,GWAS_ID_12206,GWAS_ID_12207,GWAS_ID_12208,GWAS_ID_12209,GWAS_ID_12210,GWAS_ID_12211,GWAS_ID_12212,GWAS_ID_12213 RMVar_hsa_circ_59688 110279 RMVar_ID_110279 Human_SNP_ID_800060487 m1A Human chr1 + 149887126 149887126 149887126 CGCGGAGCGGGTGGGGGCCGGCGCGCCCGTCTACATGGCGGCGGTCCTCGAGTACCTGACCGCCG CGCGGAGCGGGTGGGGGCCGGCGCGCCCGTCTGCATGGCGGCGGTCCTCGAGTACCTGACCGCCG A G H2AC20 Ensembl:ENSG00000184260 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:149887101..149887125 26863196 MeRIP-seq:(Medium) rs1553759892 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_224656,Human_RBP_ID_325116,Human_RBP_ID_970834,Human_RBP_ID_4080645,Human_RBP_ID_17724654,Human_RBP_ID_18428476,Human_RBP_ID_22428565,Human_RBP_ID_22779755,Human_RBP_ID_26389712,Human_RBP_ID_26840698,Human_RBP_ID_27167322 110280 RMVar_ID_110280 Human_SNP_ID_800060542 m1A Human chr1 - 211260308 211260308 211260308 CTGCCCACACGCCCAGTGTCACAGCCCGGCCAAGCCTGACAGCCTCCCCGCCACGGATGCCTGCC CTGCCCACACGCCCAGTGTCACAGCCCGGCCATGCCTGACAGCCTCCCCGCCACGGATGCCTGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:211260272..211260569 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110281 RMVar_ID_110281 Human_SNP_ID_800063679 m1A Human chr1 + 156114832 156114832 156114832 CAAGCCGAGAGCCAGCCGGCCGGCGCACTCCGACTCCGAGCAGTCTCTGTCCTTCGACCCGAGCC CAAGCCGAGAGCCAGCCGGCCGGCGCACTCCGGCTCCGAGCAGTCTCTGTCCTTCGACCCGAGCC A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr1:156114781..156114882 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_22148,Human_RBP_ID_4074495,Human_RBP_ID_22486073,Human_RBP_ID_22532156,Human_RBP_ID_27389260 Human_miRNA_ID_3085154 RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 110282 RMVar_ID_110282 Human_SNP_ID_800065277 m1A Human chr1 - 956932 956932 956932 GGCTGAAGGGGAAGAAGAATTCTGTTCCTGTGACCGTCGCCATGGTTGAGAGATGGAAGCAGGCA GGCTGAAGGGGAAGAAGAATTCTGTTCCTGTGGCCGTCGCCATGGTTGAGAGATGGAAGCAGGCA T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_273403,Human_RBP_ID_364596,Human_RBP_ID_851050,Human_RBP_ID_1436316,Human_RBP_ID_3932379,Human_RBP_ID_4068423,Human_RBP_ID_5109338,Human_RBP_ID_5332436,Human_RBP_ID_8320952,Human_RBP_ID_8752602,Human_RBP_ID_8976623,Human_RBP_ID_9269498,Human_RBP_ID_9342456,Human_RBP_ID_9355280,Human_RBP_ID_11137932,Human_RBP_ID_17763252,Human_RBP_ID_18964343,Human_RBP_ID_24541752,Human_RBP_ID_26309603 Human_Splice_Rec_1058,Human_Splice_Rec_1059,Human_Splice_Rec_1098,Human_Splice_Rec_1099,Human_Splice_Rec_1136,Human_Splice_Rec_1137 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_287123,RMVar_hsa_circ_319101,RMVar_hsa_circ_128246,RMVar_hsa_circ_128248,RMVar_hsa_circ_26366,RMVar_hsa_circ_310892 110283 RMVar_ID_110283 Human_SNP_ID_800065496 m1A Human chr1 + 19384271 19384271 19384271 GCCCCCACTGCCCTCCCCTCACTGCCTTCTCCACCTCTGGCCTTCTGCCAGCTCCATCCTGGTGA GCCCCCACTGCCCTCCCCTCACTGCCTTCTCCCCCTCTGGCCTTCTGCCAGCTCCATCCTGGTGA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19384268..19384393 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110284 RMVar_ID_110284 Human_SNP_ID_800069791 m1A Human chr1 - 228406641 228406641 228406641 GAGTGCCCGAGCCTGCGCCGCCGCACCCGGATACCCCGCGTCCCCGCGAGCTGCCGAGGCCGCCC GAGTGCCCGAGCCTGCGCCGCCGCACCCGGATCCCCCGCGTCCCCGCGAGCTGCCGAGGCCGCCC T G TRIM11 Ensembl:ENSG00000154370 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:228406476..228406825 26863410 MeRIP-seq:(Medium) rs930627673 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4030278,Human_RBP_ID_5338997,Human_RBP_ID_9320397 RMVar_hsa_circ_122104,RMVar_hsa_circ_140245 110285 RMVar_ID_110285 Human_SNP_ID_800081955 m1A Human chr1 + 169111461 169111461 169111461 ACCATCCAAGTGATGCTGCTCACCATCAGTGAATTTAAGCCCACATATCAGGACCGAGTGGCCCC ACCATCCAAGTGATGCTGCTCACCATCAGTGAGTTTAAGCCCACATATCAGGACCGAGTGGCCCC A G ATP1B1 Ensembl:ENSG00000143153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:169111329..169111540 26863196 MeRIP-seq:(Medium) rs557213061 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_332441,Human_RBP_ID_22429859 Human_Splice_Rec_155326,Human_Splice_Rec_155327,Human_Splice_Rec_155334,Human_Splice_Rec_155335,Human_Splice_Rec_155342,Human_Splice_Rec_155343 Human_miRNA_ID_455232,Human_miRNA_ID_457185,Human_miRNA_ID_732169,Human_miRNA_ID_2147746,Human_miRNA_ID_2148545,Human_miRNA_ID_2296769 RMVar_hsa_circ_137426,RMVar_hsa_circ_82070,RMVar_hsa_circ_137425,RMVar_hsa_circ_68623 110286 RMVar_ID_110286 Human_SNP_ID_800085737 m1A Human chr1 + 228341474 228341474 228341474 CAGCATCGACCTGAACGACCAGGTGGAGGGGGATGACCGCGCCTTCGAGGTGTGGCAGGAGCGGG CAGCATCGACCTGAACGACCAGGTGGAGGGGGGTGACCGCGCCTTCGAGGTGTGGCAGGAGCGGG A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228341449..228341527 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney Human_Splice_Rec_195368,Human_Splice_Rec_195526,Human_Splice_Rec_195754,Human_Splice_Rec_196030,Human_Splice_Rec_196256,Human_Splice_Rec_196460,Human_Splice_Rec_196664,Human_Splice_Rec_196838,Human_Splice_Rec_196862 RMVar_hsa_circ_268744,RMVar_hsa_circ_100633,RMVar_hsa_circ_140242,RMVar_hsa_circ_140243,RMVar_hsa_circ_124561,RMVar_hsa_circ_267772 110287 RMVar_ID_110287 Human_SNP_ID_800088852 m1A Human chr1 - 52033328 52033328 52033328 GCGGCCACGCGCTGAGGAGGACGGGAGAGCCCAGGCGGCGGGCAGCAGCGTCCTCAGGGAACTGC GCGGCCACGCGCTGAGGAGGACGGGAGAGCCCGGGCGGCGGGCAGCAGCGTCCTCAGGGAACTGC T C AL445685.3,KTI12,TXNDC12 Ensembl:ENSG00000285839,Ensembl:ENSG00000198841,Ensembl:ENSG00000117862 Protein coding,Protein coding,Protein coding CDS,CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:52033281..52033394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 110288 RMVar_ID_110288 Human_SNP_ID_800096057 m1A Human chr1 + 150294382 150294382 150294382 GGTTTAAATCCAAGGTCATGGCAAAACATCTGAAGTTCATCGCCAGGACTGTGATGGTACAGGAA GGTTTAAATCCAAGGTCATGGCAAAACATCTGCAGTTCATCGCCAGGACTGTGATGGTACAGGAA A C MRPS21 Ensembl:ENSG00000266472 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_2092802,Human_RBP_ID_9356780,Human_RBP_ID_24745938,Human_RBP_ID_26309803,Human_RBP_ID_26389733 Human_Splice_Rec_126226,Human_Splice_Rec_126227,Human_Splice_Rec_126229 Human_miRNA_ID_2284260,Human_miRNA_ID_2287259 110289 RMVar_ID_110289 Human_SNP_ID_800101436 m1A Human chr1 - 9734075 9734075 9734075 GACCTGGATACCTGTGAGGTCACGGTGGAGGGAGAGGAGCTGAACCACGAGCAGGAGAGCCTGGA GACCTGGATACCTGTGAGGTCACGGTGGAGGGGGAGGAGCTGAACCACGAGCAGGAGAGCCTGGA T C CLSTN1 Ensembl:ENSG00000171603 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:9734026..9734150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_222889,Human_RBP_ID_8323081,Human_RBP_ID_8978015,Human_RBP_ID_23423566,Human_RBP_ID_26310158,Human_RBP_ID_27188181 Human_Splice_Rec_15066,Human_Splice_Rec_15102,Human_Splice_Rec_15134,Human_Splice_Rec_15168 RMVar_hsa_circ_85258,RMVar_hsa_circ_121065,RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_128821,RMVar_hsa_circ_128822,RMVar_hsa_circ_15648,RMVar_hsa_circ_91160,RMVar_hsa_circ_15408,RMVar_hsa_circ_128824 110290 RMVar_ID_110290 Human_SNP_ID_800107834 m1A Human chr1 - 156938910 156938909 156938910 GCCAATAGATGAGCCCAGGGAGGAAGGTCCCCACCCCGGGAAGAGTGGGCTGGTCTGAGAGGGTG GCCAATAGATGAGCCCAGGGAGGAAGGTCCCC_CCCCGGGAAGAGTGGGCTGGTCTGAGAGGGTG GT G ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156938903..156939084 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_801797,Human_RBP_ID_21961522 RMVar_hsa_circ_1516,RMVar_hsa_circ_82735,RMVar_hsa_circ_136921 110291 RMVar_ID_110291 Human_SNP_ID_800125512 m1A Human chr1 + 155313374 155313374 155313374 TTTCATTAGTGGCAGGGGGACTGGGTTCTGGGAGGGGTGCCATGCCCGAGGAGGGTGGCAGTGAG TTTCATTAGTGGCAGGGGGACTGGGTTCTGGGGGGGGTGCCATGCCCGAGGAGGGTGGCAGTGAG A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155313351..155313800 26863196 MeRIP-seq:(Medium) rs918067132 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_222637,Human_RBP_ID_743738,Human_RBP_ID_802499,Human_RBP_ID_5694299,Human_RBP_ID_8052775,Human_RBP_ID_22870960 RMVar_hsa_circ_101793,RMVar_hsa_circ_99858,RMVar_hsa_circ_136560,RMVar_hsa_circ_136562,RMVar_hsa_circ_105685,RMVar_hsa_circ_49079,RMVar_hsa_circ_136563 110292 RMVar_ID_110292 Human_SNP_ID_800177916 m1A Human chr1 + 32202026 32202026 32202026 CCCCAGGCACACTACGGAGGGTCCCTGTGCCTACCAGCCACAGCGGCTCCTTGGCCCTAGGACTT CCCCAGGCACACTACGGAGGGTCCCTGTGCCTCCCAGCCACAGCGGCTCCTTGGCCCTAGGACTT A C CCDC28B Ensembl:ENSG00000160050 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:32202001..32202025 26863196 MeRIP-seq:(Medium) rs200013564 Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 2 ovary Human_RBP_ID_4045405,Human_RBP_ID_9318801 Human_Splice_Rec_42783,Human_Splice_Rec_42793,Human_Splice_Rec_42797,Human_Splice_Rec_42805,Human_Splice_Rec_42813 110293 RMVar_ID_110293 Human_SNP_ID_800183387 m1A Human chr1 - 16569139 16569139 16569139 TCTCAATTCCTCCTGAAATGTTGGCCTCGTACAAGTCTTACAGCGGCACATTTCACTCATTAGAG TCTCAATTCCTCCTGAAATGTTGGCCTCGTACCAGTCTTACAGCGGCACATTTCACTCATTAGAG T G NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs849614 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,head_neck squamous_cell_carcinoma 47 head and neck Human_Splice_Rec_22534,Human_Splice_Rec_22535,Human_Splice_Rec_22588,Human_Splice_Rec_22589,Human_Splice_Rec_22624,Human_Splice_Rec_22625 Human_miRNA_ID_2657998,Human_miRNA_ID_2743256 RMVar_hsa_circ_107471,RMVar_hsa_circ_129548 110294 RMVar_ID_110294 Human_SNP_ID_800186305 m1A Human chr1 + 20594385 20594385 20594385 CATTCGTGACTGCTTGTGGGGAGAGCCGAGGGAGAGGTACAGAAAGAGGAGCTCACTGGTGAGGA CATTCGTGACTGCTTGTGGGGAGAGCCGAGGGCGAGGTACAGAAAGAGGAGCTCACTGGTGAGGA A C CDA Ensembl:ENSG00000158825 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:20594383..20594548 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110295 RMVar_ID_110295 Human_SNP_ID_800189991 m1A Human chr1 + 40879085 40879082 40879085 AGGAAAGAAGGAAGGAAGGAAGGAAGGAAGAAAGAAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA AGGAAAGAAGGAAGGAAGGAAGGAAGGAAG___GAAAGAAAAAGAAAGAAAGAAAAAAGAAAAGA GAAA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:40879035..40879119 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 PAAD 1 - 110296 RMVar_ID_110296 Human_SNP_ID_800197576 m1A Human chr1 - 40625455 40625455 40625455 TGTTGAGGATCCCATCTGACATTTGGGGATTCACTGCATGAAGTTGTTCATTTGGGGCTCCAGTT TGTTGAGGATCCCATCTGACATTTGGGGATTCGCTGCATGAAGTTGTTCATTTGGGGCTCCAGTT T C RIMS3 Ensembl:ENSG00000117016 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs570671 Functional Loss SNV ICGC 33..33 33 LUSC 2 - GWAS_ID_11158,GWAS_ID_11159 RMVar_hsa_circ_103480,RMVar_hsa_circ_265425,RMVar_hsa_circ_132051,RMVar_hsa_circ_91202,RMVar_hsa_circ_132050 110297 RMVar_ID_110297 Human_SNP_ID_800199847 m1A Human chr1 - 184754584 184754583 184754584 TCCCCGGTTCCCCAGCGAGCGCGATGGAGACTAGTGGCGGCGACGGCCGCGTTCTGCCTGGTGTC TCCCCGGTTCCCCAGCGAGCGCGATGGAGACT_GTGGCGGCGACGGCCGCGTTCTGCCTGGTGTC CT C EDEM3 Ensembl:ENSG00000116406 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:184754533..184754827 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 KIRP 2 - Human_RBP_ID_4073206,Human_RBP_ID_5312775,Human_RBP_ID_8754285 Human_Splice_Rec_166093,Human_Splice_Rec_166131,Human_Splice_Rec_166193 110298 RMVar_ID_110298 Human_SNP_ID_800214765 m1A Human chr1 - 1272638 1272638 1272638 CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGATGAGTGACAGGCAGGTGACCCAGGCAGGTGCA CAGGCAGGTGAGCCAGGCAGGTAGGTGCGTGGGTGAGTGACAGGCAGGTGACCCAGGCAGGTGCA T C UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1272636..1272748 26863196 MeRIP-seq:(Medium) rs1356782589 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_741080,Human_RBP_ID_1064383,Human_RBP_ID_3327871,Human_RBP_ID_8051309,Human_RBP_ID_10552390,Human_RBP_ID_18415204,Human_RBP_ID_23263245 RMVar_hsa_circ_105699,RMVar_hsa_circ_128299 110299 RMVar_ID_110299 Human_SNP_ID_800217338 m1A Human chr1 - 201488984 201488984 201488984 AGTCACCTCACCCCATGCCCTTCTCCATGCAGAGCCCCTGGCCACAGGCCCACCACCAACCCCAA AGTCACCTCACCCCATGCCCTTCTCCATGCAGTGCCCCTGGCCACAGGCCCACCACCAACCCCAA T A CSRP1 Ensembl:ENSG00000159176 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201488951..201489000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 9 lung Human_Splice_Rec_172866,Human_Splice_Rec_172878,Human_Splice_Rec_172886,Human_Splice_Rec_172894,Human_Splice_Rec_172904,Human_Splice_Rec_172910,Human_Splice_Rec_172924,Human_Splice_Rec_172932,Human_Splice_Rec_172942,Human_Splice_Rec_172958,Human_Splice_Rec_172968,Human_Splice_Rec_172976,Human_Splice_Rec_172984,Human_Splice_Rec_172990 RMVar_hsa_circ_2569,RMVar_hsa_circ_86124,RMVar_hsa_circ_127254,RMVar_hsa_circ_138806,RMVar_hsa_circ_138807,RMVar_hsa_circ_138809,RMVar_hsa_circ_295982 110300 RMVar_ID_110300 Human_SNP_ID_800222578 m1A Human chr1 - 149944204 149944204 149944204 GTCCATGTGTCGGGGGCCTACCACCATATGCCACCTTCCCCAGACAGTGCCCTCCTGGGCGACCC GTCCATGTGTCGGGGGCCTACCACCATATGCCTCCTTCCCCAGACAGTGCCCTCCTGGGCGACCC T A OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:149944153..149944237 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_26367696,Human_RBP_ID_27387569 110301 RMVar_ID_110301 Human_SNP_ID_800222856 m1A Human chr1 + 117103122 117103122 117103122 GAAGATTACAAGGCCCTAGGGAAGGTGAAGCCACTAGCTCAGCAGTTCTTAGCCTAGTTTTTGGC GAAGATTACAAGGCCCTAGGGAAGGTGAAGCCGCTAGCTCAGCAGTTCTTAGCCTAGTTTTTGGC A G TTF2 Ensembl:ENSG00000116830 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9728670 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver GWAS_ID_8448,GWAS_ID_8449 110302 RMVar_ID_110302 Human_SNP_ID_800232963 m1A Human chr1 + 171535548 171535548 171535548 GTCTCAACCTCGGCCGGCTGTATTATCTGGCTATTTCAAACAGTTTCAGAAGTCTTTACCTCCAC GTCTCAACCTCGGCCGGCTGTATTATCTGGCTGTTTCAAACAGTTTCAGAAGTCTTTACCTCCAC A G PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:171535372..171535600 26863196 MeRIP-seq:(Medium) rs1414744292 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_1729099,Human_RBP_ID_8737849,Human_RBP_ID_9359583,Human_RBP_ID_17213725,Human_RBP_ID_17331423,Human_RBP_ID_26846806 Human_Splice_Rec_157283,Human_Splice_Rec_157349,Human_Splice_Rec_157425 Human_miRNA_ID_2646686,Human_miRNA_ID_2669279,Human_miRNA_ID_3099927 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_137540,RMVar_hsa_circ_97212,RMVar_hsa_circ_356800,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_373034,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_364102,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_318239,RMVar_hsa_circ_319804,RMVar_hsa_circ_280025,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_137546 110303 RMVar_ID_110303 Human_SNP_ID_800244167 m1A Human chr1 + 151254795 151254795 151254795 GGAGGGAGGAAGGTGGCAAGATGGTGTTGGAAAGCACTATGGTGTGGTGAGGAGCTACTTCGGGG GGAGGGAGGAAGGTGGCAAGATGGTGTTGGAAGGCACTATGGTGTGGTGAGGAGCTACTTCGGGG A G PSMD4 Ensembl:ENSG00000159352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:151254726..151259106;chr1:151254751..151254905 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_326203,Human_RBP_ID_745283,Human_RBP_ID_4073020,Human_RBP_ID_18187263,Human_RBP_ID_18415995,Human_RBP_ID_22430909,Human_RBP_ID_23205330,Human_RBP_ID_23332276,Human_RBP_ID_26311804 Human_Splice_Rec_128901,Human_Splice_Rec_128919,Human_Splice_Rec_128937,Human_Splice_Rec_128939,Human_Splice_Rec_128947 110304 RMVar_ID_110304 Human_SNP_ID_800250367 m1A Human chr1 + 202348859 202348859 202348859 GGCAGCAGCTGCCGAGGCCGGAGCAATGGCGGAACTGGAGCACCTAGGAGGGAAGCGGGCAGAGT GGCAGCAGCTGCCGAGGCCGGAGCAATGGCGGTACTGGAGCACCTAGGAGGGAAGCGGGCAGAGT A T PPP1R12B Ensembl:ENSG00000077157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:202348748..202348961 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_853157,Human_RBP_ID_4017206,Human_RBP_ID_5413397,Human_RBP_ID_5519963,Human_RBP_ID_10727563,Human_RBP_ID_18410276,Human_RBP_ID_18415129,Human_RBP_ID_18966317,Human_RBP_ID_22024099,Human_RBP_ID_26315889 RMVar_hsa_circ_138922,RMVar_hsa_circ_92737 110305 RMVar_ID_110305 Human_SNP_ID_800261560 m1A Human chr1 + 151369768 151369768 151369768 GAGTAGCCGGGTCCACAATTCCCACATTTCGTAGCTGTGGAAGCAATGGGGCGCATTGGCTGGGC GAGTAGCCGGGTCCACAATTCCCACATTTCGTCGCTGTGGAAGCAATGGGGCGCATTGGCTGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:151369701..151369775;chr1:151369400..151369775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney 110306 RMVar_ID_110306 Human_SNP_ID_800266672 m1A Human chr1 + 161038664 161038664 161038664 AGGCTAGGAGTGAACGGAGTTCAGGAAGCGAGACCGTGGGCGCTGAGGAAGGGGCGCGACAGCCT AGGCTAGGAGTGAACGGAGTTCAGGAAGCGAGGCCGTGGGCGCTGAGGAAGGGGCGCGACAGCCT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:161038634..161038897 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110307 RMVar_ID_110307 Human_SNP_ID_800272003 m1A Human chr1 + 181089672 181089672 181089672 AGAGCAGCCGCCGAGTGGAGGAGAGGACGACGACGCGGAGGAGATGGAGACCGGGAACGTGGCTA AGAGCAGCCGCCGAGTGGAGGAGAGGACGACGTCGCGGAGGAGATGGAGACCGGGAACGTGGCTA A T IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:181089160..181089995 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_4011534,Human_RBP_ID_5724844,Human_RBP_ID_22870999 110308 RMVar_ID_110308 Human_SNP_ID_800283193 m1A Human chr1 - 32651324 32651324 32651324 CACTGCCCTCCTGGGTCGGCCCCGGCACCCTCACCTTCCTTGTCGGCCATGGCGGGCAGGCGAGC CACTGCCCTCCTGGGTCGGCCCCGGCACCCTCCCCTTCCTTGTCGGCCATGGCGGGCAGGCGAGC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:32651201..32651388 26863196 MeRIP-seq:(Medium) rs530899496 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110309 RMVar_ID_110309 Human_SNP_ID_800283340 m1A Human chr1 - 58577210 58577210 58577210 AGACCATCCCAGACGCCGGAGCCCGAGCCCCGACGAGTCCCCGCGCCTCATCCGCCCGCGTCCGG AGACCATCCCAGACGCCGGAGCCCGAGCCCCGCCGAGTCCCCGCGCCTCATCCGCCCGCGTCCGG T G TACSTD2 Ensembl:ENSG00000184292 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58576963..58577337 26863196 MeRIP-seq:(Medium) rs232835 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Clinvar_Rec_625 110310 RMVar_ID_110310 Human_SNP_ID_800297601 m1A Human chr1 + 233666708 233666708 233666708 TCCTGTTCCTGACGGCTGTGGTCCAGCGCATCACCGTGCACGTCACCCGCAGGCCGGTCCTCTAC TCCTGTTCCTGACGGCTGTGGTCCAGCGCATCGCCGTGCACGTCACCCGCAGGCCGGTCCTCTAC A G KCNK1 Ensembl:ENSG00000135750 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:233666557..233666850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110311 RMVar_ID_110311 Human_SNP_ID_800304684 m1A Human chr1 + 223712875 223712875 223712875 GCAAAACCCGGGGCATCGAGTGGAAGCGCCCCACGGTAGGAAGCGCGCGGCAGGACGCGGGCAGG GCAAAACCCGGGGCATCGAGTGGAAGCGCCCCGCGGTAGGAAGCGCGCGGCAGGACGCGGGCAGG A G CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:223712826..223712900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung Human_RBP_ID_342614,Human_RBP_ID_856691 Human_Splice_Rec_190627 RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 110312 RMVar_ID_110312 Human_SNP_ID_800306986 m1A Human chr1 + 111691353 111691353 111691353 GTTTGTTTTTCAGATCGTCAGTATTTAAACAGATCACATCATGCGTGAGTACAAGCTAGTGGTCC GTTTGTTTTTCAGATCGTCAGTATTTAAACAGGTCACATCATGCGTGAGTACAAGCTAGTGGTCC A G RAP1A Ensembl:ENSG00000116473 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:111619794..111691425;chr1:111619790..111697441 26863196 MeRIP-seq:(Medium) rs144405448 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_857036,Human_RBP_ID_4074276,Human_RBP_ID_8940003,Human_RBP_ID_26311615,Human_RBP_ID_27800622 Human_Splice_Rec_109576,Human_Splice_Rec_109577,Human_Splice_Rec_109592,Human_Splice_Rec_109593,Human_Splice_Rec_109602,Human_Splice_Rec_109603,Human_Splice_Rec_109616,Human_Splice_Rec_109617 RMVar_hsa_circ_119682,RMVar_hsa_circ_333183,RMVar_hsa_circ_135300,RMVar_hsa_circ_342534,RMVar_hsa_circ_334779,RMVar_hsa_circ_283654,RMVar_hsa_circ_135302,RMVar_hsa_circ_103032,RMVar_hsa_circ_135303,RMVar_hsa_circ_135301 110313 RMVar_ID_110313 Human_SNP_ID_800313702 m1A Human chr1 - 21426289 21426289 21426289 CCAGAACTGCCTGATTCATGCCAGCCCTACGGAAGTTGCTTTTACTCATTGGAGGAAGAACACGT CCAGAACTGCCTGATTCATGCCAGCCCTACGGCAGTTGCTTTTACTCATTGGAGGAAGAACACGT T G NBPF2P Ensembl:ENSG00000227001 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs140348908 Functional Loss SNV ICGC 33..33 33 COCA 6 - RMVar_hsa_circ_108762,RMVar_hsa_circ_130049,RMVar_hsa_circ_103959,RMVar_hsa_circ_130048 110314 RMVar_ID_110314 Human_SNP_ID_800315786 m1A Human chr1 - 8360710 8360710 8360710 CCTTGGCCATGCCCCACATCAAGCCCCCGCCTACCACTCCCATCCCCCAGCTGCCGGCGCCACAG CCTTGGCCATGCCCCACATCAAGCCCCCGCCTGCCACTCCCATCCCCCAGCTGCCGGCGCCACAG T C RERE Ensembl:ENSG00000142599 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:8360497..8360946 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_4066643,Human_RBP_ID_5125133,Human_RBP_ID_17070987,Human_RBP_ID_17337933,Human_RBP_ID_18929204 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128716 110315 RMVar_ID_110315 Human_SNP_ID_800323631 m1A Human chr1 + 2229577 2229577 2229577 TGGTGCACTCGCACAAGGCCCTGGAGAACCGGACCTGCCACTGGGGCTTCGACTCGGCCAACTGG TGGTGCACTCGCACAAGGCCCTGGAGAACCGGCCCTGCCACTGGGGCTTCGACTCGGCCAACTGG A C SKI Ensembl:ENSG00000157933 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:2229526..2229725 26863196 MeRIP-seq:(Medium) rs201274840 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,lung small_cell_carcinoma 2 lung Human_RBP_ID_25337,Human_RBP_ID_8743102,Human_RBP_ID_9357913,Human_RBP_ID_26852532,Human_RBP_ID_27175333,Human_RBP_ID_27393921 110316 RMVar_ID_110316 Human_SNP_ID_800324555 m1A Human chr1 - 226383093 226383093 226383093 TCCCCCCAGAAACCAGCGCCTCCGTGGCGGCCACGCCTCCGCCCTCCACAGCCTCGGCTCCTGCT TCCCCCCAGAAACCAGCGCCTCCGTGGCGGCCCCGCCTCCGCCCTCCACAGCCTCGGCTCCTGCT T G PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226383002..226383141 26863196 MeRIP-seq:(Medium) rs1393949279 Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_222359,Human_RBP_ID_4090047,Human_RBP_ID_8744232,Human_RBP_ID_9270689,Human_RBP_ID_9357614,Human_RBP_ID_22427843,Human_RBP_ID_22782480,Human_RBP_ID_24528825,Human_RBP_ID_26376362,Human_RBP_ID_26855024,Human_RBP_ID_27176803 Human_Splice_Rec_193268,Human_Splice_Rec_193269 RMVar_hsa_circ_118459,RMVar_hsa_circ_140108 110317 RMVar_ID_110317 Human_SNP_ID_800375648 m1A Human chr1 + 19339407 19339407 19339407 TATTCTCAGGGAGAGATGGCGCTGTGCGGTCAATGATGCAGCTGTTATGTGACCTGTCGGGGAGG TATTCTCAGGGAGAGATGGCGCTGTGCGGTCACTGATGCAGCTGTTATGTGACCTGTCGGGGAGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:19339218..19339560;chr1:19339126..19339531 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110318 RMVar_ID_110318 Human_SNP_ID_800377787 m1A Human chr1 + 32334449 32334447 32334450 AGATGGCTGATGGGAGAATCCACAGGAGGGAGAGGAGGAAAGGGAACGTGGCTGGGAGGAGGCAA AGATGGCTGATGGGAGAATCCACAGGAGGGA___GAGGAAAGGGAACGTGGCTGGGAGGAGGCAA AGAG A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:32334348..32334544 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - 110319 RMVar_ID_110319 Human_SNP_ID_800384581 m1A Human chr1 + 55040015 55040015 55040015 AGGACGGCCTGGCCGAAGCACCCGAGCACGGAACCACAGCCACCTTCCACCGCTGCGCCAAGGTG AGGACGGCCTGGCCGAAGCACCCGAGCACGGATCCACAGCCACCTTCCACCGCTGCGCCAAGGTG A T PCSK9 Ensembl:ENSG00000169174 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:55039551..55040071 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_746035,Human_RBP_ID_9320046,Human_RBP_ID_22428408 Human_Splice_Rec_75139,Human_Splice_Rec_75149 Human_miRNA_ID_1422268 110320 RMVar_ID_110320 Human_SNP_ID_800386141 m1A Human chr1 + 50970411 50970410 50970411 CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCCAGGGGGGACCTAGAGCAACTTACTAGTTTGTTG CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCC_GGGGGGACCTAGAGCAACTTACTAGTTTGTTG CA C CDKN2C Ensembl:ENSG00000123080 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:50970251..50970455 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 GBM 1 - Human_RBP_ID_5836072,Human_RBP_ID_17753373,Human_RBP_ID_26388203 Human_Splice_Rec_68556,Human_Splice_Rec_68557,Human_Splice_Rec_68560,Human_Splice_Rec_68561,Human_Splice_Rec_68563 RMVar_hsa_circ_11687 110321 RMVar_ID_110321 Human_SNP_ID_800392985 m1A Human chr1 + 201213477 201213477 201213477 GGTGCCTGGAGGAGATGCTGAATGAAGATCAGAGCCGGGAGCCCCCTGGTCACCTTGGTAGCAGG GGTGCCTGGAGGAGATGCTGAATGAAGATCAGCGCCGGGAGCCCCCTGGTCACCTTGGTAGCAGG A C IGFN1 Ensembl:ENSG00000163395 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:201213429..201213536 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 2 pancreas 110322 RMVar_ID_110322 Human_SNP_ID_800393119 m1A Human chr1 + 228416718 228416718 228416718 TGGCGTCAGCGGGGGCTGGGGGGCGGCGGGGGAGGGGAATGCTGGGCGAGGGAGTGTTCGGCGGC TGGCGTCAGCGGGGGCTGGGGGGCGGCGGGGGGGGGGAATGCTGGGCGAGGGAGTGTTCGGCGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228416460..228416871 26863196 MeRIP-seq:(Medium) rs1378078307 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110323 RMVar_ID_110323 Human_SNP_ID_800397617 m1A Human chr1 + 11077440 11077440 11077440 GCAGTCGTGAGGTCCAAAGAGAACATTCTCCAATCTCTGCATTAAAAGACACCAGCAGGCTGGCA GCAGTCGTGAGGTCCAAAGAGAACATTCTCCAGTCTCTGCATTAAAAGACACCAGCAGGCTGGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:11077355..11077455 32194978 MeRIP-seq:(Medium) rs1553165516 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 110324 RMVar_ID_110324 Human_SNP_ID_800399626 m1A Human chr1 - 154263175 154263175 154263175 CTTCAGTGCAAATTTATACACACACACAAAACACAGCCCCCAGCCTTGGGCCAAATTAGCTCTCA CTTCAGTGCAAATTTATACACACACACAAAACGCAGCCCCCAGCCTTGGGCCAAATTAGCTCTCA T C lnc-C1orf43-4 RNACentral:URS00008B58D2 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154263151..154263175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 110325 RMVar_ID_110325 Human_SNP_ID_800399804 m1A Human chr1 + 1482194 1482194 1482194 TGCGGCACAAGAATGAGATGCTGCGAGTGGAGACCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG TGCGGCACAAGAATGAGATGCTGCGAGTGGAGGCCGAGGCCCGGGCGCGCGCCAAGGCCGAGCGG A G ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1482141..1482295 26863196 MeRIP-seq:(Medium) rs747464654 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_804487,Human_RBP_ID_3932508,Human_RBP_ID_9355314,Human_RBP_ID_10556369,Human_RBP_ID_18966828,Human_RBP_ID_22871683,Human_RBP_ID_26309997,Human_RBP_ID_27797257 Human_Splice_Rec_4134,Human_Splice_Rec_4186,Human_Splice_Rec_4210 RMVar_hsa_circ_103406,RMVar_hsa_circ_92996,RMVar_hsa_circ_128329,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_123638,RMVar_hsa_circ_125206,RMVar_hsa_circ_125077,RMVar_hsa_circ_109226,RMVar_hsa_circ_3673,RMVar_hsa_circ_128334,RMVar_hsa_circ_128336,RMVar_hsa_circ_128337,RMVar_hsa_circ_128335,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_349219,RMVar_hsa_circ_128339,RMVar_hsa_circ_34002,RMVar_hsa_circ_128340,RMVar_hsa_circ_102351,RMVar_hsa_circ_128341 110326 RMVar_ID_110326 Human_SNP_ID_800415141 m1A Human chr1 - 43981441 43981441 43981441 CAAGACCAGGTGGCGAGTCAGGACAGGGTGGCAGCGTGGGAGCCGTGGGACCGGGCAGGGCACTG CAAGACCAGGTGGCGAGTCAGGACAGGGTGGCGGCGTGGGAGCCGTGGGACCGGGCAGGGCACTG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:43981343..43981475 26863196 MeRIP-seq:(Medium) rs375270042 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus RMVar_hsa_circ_86054,RMVar_hsa_circ_132368 110327 RMVar_ID_110327 Human_SNP_ID_800419473 m1A Human chr1 - 45013188 45013188 45013188 CTCACCTGCAGAGTCAGTTCACAGCAGGCCTCAGGAGAGCGACACGTGCTGAAAAAGTCCTGGGC CTCACCTGCAGAGTCAGTTCACAGCAGGCCTCCGGAGAGCGACACGTGCTGAAAAAGTCCTGGGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45012945..45013375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 110328 RMVar_ID_110328 Human_SNP_ID_800421932 m1A Human chr1 - 25338004 25338004 25338004 GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGAGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT GCGCAGCCCTCTCAGGGGTGGGTGGCAGGAAGCGTGCCGGGTCCCGCGTGGTGCAAAAGGTGGGT T G RSRP1 Ensembl:ENSG00000117616 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:25337992..25338104 26863196 MeRIP-seq:(Medium) rs585500 Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_22707042,Human_RBP_ID_24359574,Human_RBP_ID_26772990,Human_RBP_ID_27571565 Human_Splice_Rec_32077 110329 RMVar_ID_110329 Human_SNP_ID_800423757 m1A Human chr1 + 180198305 180198305 180198305 TCCTGCCTCAGTGCCCTGGGCTGGTGAGGGAGAAGCCTGTCTGCACCTGCCTAATTCCAGCTCCT TCCTGCCTCAGTGCCCTGGGCTGGTGAGGGAGGAGCCTGTCTGCACCTGCCTAATTCCAGCTCCT A G QSOX1 Ensembl:ENSG00000116260 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:180198254..180198354 32194978 MeRIP-seq:(Medium) rs3843273 Functional Loss SNV ICGC,COSMIC 33..33 33 head_neck squamous_cell_carcinoma,ESCA 7 head and neck GWAS_ID_8379,GWAS_ID_8380,GWAS_ID_8381 110330 RMVar_ID_110330 Human_SNP_ID_800425582 m1A Human chr1 + 95072852 95072852 95072852 GAAGCACTACCCATATTCGCAGGATTAGGAAAACCGCCACAGCTCCTGCGGCCGCAGCTAGAACG GAAGCACTACCCATATTCGCAGGATTAGGAAACCCGCCACAGCTCCTGCGGCCGCAGCTAGAACG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:95072802..95072895 26863196 MeRIP-seq:(Medium) rs773486977 Functional Loss SNV COSMIC 33..33 33 pancreas adenocarcinoma 1 pancreas 110331 RMVar_ID_110331 Human_SNP_ID_800429956 m1A Human chr1 + 155327126 155327126 155327126 GGGCCCCGCAGAAAATGAGAATGGAGCCCTAAAGTCCAGGTAATGGGGTACCTTGTCCTTTCTAT GGGCCCCGCAGAAAATGAGAATGGAGCCCTAAGGTCCAGGTAATGGGGTACCTTGTCCTTTCTAT A G RUSC1 Ensembl:ENSG00000160753 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155327076..155327150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_857501,Human_RBP_ID_3936749,Human_RBP_ID_5338531,Human_RBP_ID_18969063,Human_RBP_ID_19035505,Human_RBP_ID_23335077,Human_RBP_ID_26386502 Human_Splice_Rec_138715,Human_Splice_Rec_138733,Human_Splice_Rec_138771,Human_Splice_Rec_138795,Human_Splice_Rec_138811,Human_Splice_Rec_138833,Human_Splice_Rec_138849,Human_Splice_Rec_138873,Human_Splice_Rec_138887 RMVar_hsa_circ_5170,RMVar_hsa_circ_54289,RMVar_hsa_circ_89239,RMVar_hsa_circ_125217,RMVar_hsa_circ_136567,RMVar_hsa_circ_136568 110332 RMVar_ID_110332 Human_SNP_ID_800440552 m1A Human chr1 + 30953947 30953946 30953948 CTGCGGTACTTGGCTTCAGCGCCTGGAGCAGCAGAGATGTATCTTCCACTGCCATTCGTGAGTCC CTGCGGTACTTGGCTTCAGCGCCTGGAGCAGC__AGATGTATCTTCCACTGCCATTCGTGAGTCC CAG C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:30953743..30964785 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - 110333 RMVar_ID_110333 Human_SNP_ID_800440722 m1A Human chr1 - 23168152 23168152 23168152 GGCGCGGGGCGCGGGCCGCGGGCCGGGCGGGGAGGGGTCCCGCGGCCGCCGCAGCTGTCGGCCGC GGCGCGGGGCGCGGGCCGCGGGCCGGGCGGGGGGGGGTCCCGCGGCCGCCGCAGCTGTCGGCCGC T C LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23168143..23168333 26863196 MeRIP-seq:(Medium) rs941864413 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 110334 RMVar_ID_110334 Human_SNP_ID_800443285 m1A Human chr1 - 168136816 168136816 168136816 GAAACCTCCAGTCCCGGAGCGCGGCGGGGAGGAAGGAAGCGGCGGCGGCGGTGGCCGAGGCGGGG GAAACCTCCAGTCCCGGAGCGCGGCGGGGAGGGAGGAAGCGGCGGCGGCGGTGGCCGAGGCGGGG T C GPR161 Ensembl:ENSG00000143147 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:168136689..168136920 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110335 RMVar_ID_110335 Human_SNP_ID_800448281 m1A Human chr1 - 231421270 231421270 231421270 AGTACATCGTGCCGTGCATGAACAAGCACGGCATCTGTGTGGTGGACGACTTCCTCGGCAAGGAG AGTACATCGTGCCGTGCATGAACAAGCACGGCGTCTGTGTGGTGGACGACTTCCTCGGCAAGGAG T C EGLN1,AL445524.2 Ensembl:ENSG00000135766,Ensembl:ENSG00000287856 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:231421222..231421362 26863196 MeRIP-seq:(Medium) rs760962608 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_345935,Human_RBP_ID_1423876,Human_RBP_ID_5778128,Human_RBP_ID_8745312,Human_RBP_ID_17742944,Human_RBP_ID_22025696,Human_RBP_ID_27835443 110336 RMVar_ID_110336 Human_SNP_ID_800462539 m1A Human chr1 + 180192202 180192202 180192202 GCACAGGCTGGAGACCAGCAGGTGCAAAGGACAAGCCTGGTGTGTGGGCAGCACTGAAAGAAGGC GCACAGGCTGGAGACCAGCAGGTGCAAAGGACCAGCCTGGTGTGTGGGCAGCACTGAAAGAAGGC A C QSOX1 Ensembl:ENSG00000116260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:180192199..180192576 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_10473,RMVar_hsa_circ_86078,RMVar_hsa_circ_138088,RMVar_hsa_circ_138089,RMVar_hsa_circ_95713,RMVar_hsa_circ_78194,RMVar_hsa_circ_109016,RMVar_hsa_circ_108105,RMVar_hsa_circ_138091,RMVar_hsa_circ_85642,RMVar_hsa_circ_138092,RMVar_hsa_circ_138094,RMVar_hsa_circ_65866,RMVar_hsa_circ_138095 110337 RMVar_ID_110337 Human_SNP_ID_800472112 m1A Human chr1 - 147254978 147254978 147254978 AAACAATAAAATTTCAGCTACATCTACTCTGTACCTCTGCATTTCTTCTTTCCAGTTGCTCAAAA AAACAATAAAATTTCAGCTACATCTACTCTGTGCCTCTGCATTTCTTCTTTCCAGTTGCTCAAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:147254963..147256552 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110338 RMVar_ID_110338 Human_SNP_ID_800485964 m1A Human chr1 - 220001092 220001092 220001092 CGGATATGTGTATAAAAATAAATGGTCTTTCTATCCCAGGGTTTAGAATATATTTCTTTACAGAT CGGATATGTGTATAAAAATAAATGGTCTTTCTGTCCCAGGGTTTAGAATATATTTCTTTACAGAT T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220001090..220001197 26863196 MeRIP-seq:(Medium) rs757822654 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_14262,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170,RMVar_hsa_circ_375651,RMVar_hsa_circ_267598,RMVar_hsa_circ_295947,RMVar_hsa_circ_139650,RMVar_hsa_circ_139651 110339 RMVar_ID_110339 Human_SNP_ID_800495526 m1A Human chr1 - 63367689 63367689 63367689 GGGGTCCGGAACCTCCGGGATCCCATGCTCTTACCCCGCCGCCCGCCGGCCGCTGGGATTCGCGC GGGGTCCGGAACCTCCGGGATCCCATGCTCTTCCCCCGCCGCCCGCCGGCCGCTGGGATTCGCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:63367658..63367747;chr1:63367669..63367766 26863196 MeRIP-seq:(Medium) rs940418404 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 110340 RMVar_ID_110340 Human_SNP_ID_800496521 m1A Human chr1 - 1729287 1729287 1729287 AGGGTGGCCTTGTCCACCTCCCCATCGAGAATATGGCTGCCGGCCTCTTTGAAGATTGTGGTCTG AGGGTGGCCTTGTCCACCTCCCCATCGAGAATGTGGCTGCCGGCCTCTTTGAAGATTGTGGTCTG T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1061884 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_366952,Human_RBP_ID_1073977,Human_RBP_ID_4005516,Human_RBP_ID_10635608,Human_RBP_ID_23145342,Human_RBP_ID_26370974 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 110341 RMVar_ID_110341 Human_SNP_ID_800499249 m1A Human chr1 - 154221246 154221246 154221246 AAATCGAGGCCCCGGCTCTGGCGCGGCCCACTAGGCCGCGAACCCAACCATAAACAAAACCTCCG AAATCGAGGCCCCGGCTCTGGCGCGGCCCACTGGGCCGCGAACCCAACCATAAACAAAACCTCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154221242..154221446 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 110342 RMVar_ID_110342 Human_SNP_ID_800526159 m1A Human chr1 - 155328159 155328159 155328159 GCCAACACACTCACTGTCGGGGGCAGCCAGCTAGATGGTCTCCTAAAAGAAGGGACATAGGGTCA GCCAACACACTCACTGTCGGGGGCAGCCAGCTGGATGGTCTCCTAAAAGAAGGGACATAGGGTCA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155328151..155328225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 110343 RMVar_ID_110343 Human_SNP_ID_800528986 m1A Human chr1 + 151366387 151366387 151366387 AGCGGATCTCCAAGGGAATAAGCCCATCTTTTAGAGACAGGGTCTGCACAATCTCATGGCGCTGC AGCGGATCTCCAAGGGAATAAGCCCATCTTTTGGAGACAGGGTCTGCACAATCTCATGGCGCTGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151366337..151366482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 110344 RMVar_ID_110344 Human_SNP_ID_800529888 m1A Human chr1 + 19139040 19139040 19139040 AAGACCCAAGCAGAGATTCCTGTTTTGTCCCCACCCTCTGCCCAAGGAGACAGGACCCCCGCCAT AAGACCCAAGCAGAGATTCCTGTTTTGTCCCCCCCCTCTGCCCAAGGAGACAGGACCCCCGCCAT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19139038..19139153 26863196 MeRIP-seq:(Medium) rs752425699 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110345 RMVar_ID_110345 Human_SNP_ID_800536174 m1A Human chr1 - 44029507 44029507 44029507 TTTTGAGGATGGGTAGGATACATACAGGTGGAAGTGGAGACAAGGGTGCTCAAAAAACATGGAAC TTTTGAGGATGGGTAGGATACATACAGGTGGAGGTGGAGACAAGGGTGCTCAAAAAACATGGAAC T C SLC6A9 Ensembl:ENSG00000196517 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:44029505..44029592 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 110346 RMVar_ID_110346 Human_SNP_ID_800543986 m1A Human chr1 - 63593454 63593454 63593454 TGGCGACTTGCTGCCGGGGGTCAGAGCGGCGGACTTGGCTGGCGGAGGGGCGGCCGGCTGAGGCT TGGCGACTTGCTGCCGGGGGTCAGAGCGGCGGGCTTGGCTGGCGGAGGGGCGGCCGGCTGAGGCT T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:63593326..63593700 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 110347 RMVar_ID_110347 Human_SNP_ID_800557643 m1A Human chr1 - 1729296 1729296 1729296 GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCATCGAGAATATGGCTGCCGGCCTCTTTGAAGAT GCAACTCCCAGGGTGGCCTTGTCCACCTCCCCGTCGAGAATATGGCTGCCGGCCTCTTTGAAGAT T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1061883 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_1073977,Human_RBP_ID_5541855,Human_RBP_ID_5897308,Human_RBP_ID_8171533,Human_RBP_ID_10635609,Human_RBP_ID_23145342,Human_RBP_ID_26370974 Human_miRNA_ID_2365616,Human_miRNA_ID_2365617,Human_miRNA_ID_3013421,Human_miRNA_ID_3013422 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 110348 RMVar_ID_110348 Human_SNP_ID_800559374 m1A Human chr1 - 149886536 149886536 149886536 AAAGACGGCAAGAAGCGCAAGCGCAGCCGCAAAGAGAGCTACTCCATCTACGTGTACAAGGTGCT AAAGACGGCAAGAAGCGCAAGCGCAGCCGCAAGGAGAGCTACTCCATCTACGTGTACAAGGTGCT T C H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr1:149886273..149886675;chr1:149886302..149886675 26863196 MeRIP-seq:(Medium) rs782404356 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver Human_RBP_ID_325107,Human_RBP_ID_745707,Human_RBP_ID_970826,Human_RBP_ID_1411068,Human_RBP_ID_1724777,Human_RBP_ID_3280336,Human_RBP_ID_5685322,Human_RBP_ID_9319114,Human_RBP_ID_17445787,Human_RBP_ID_18522557,Human_RBP_ID_18550706,Human_RBP_ID_22430884,Human_RBP_ID_26314617,Human_RBP_ID_26798801,Human_RBP_ID_26840691 110349 RMVar_ID_110349 Human_SNP_ID_800565786 m1A Human chr1 - 1046035 1046035 1046035 ACAGGTGAGCATCGGGCAGACACAGTGGGCTGAGCCAGACTCCTCCACGCACCGCGCACCGAACT ACAGGTGAGCATCGGGCAGACACAGTGGGCTGCGCCAGACTCCTCCACGCACCGCGCACCGAACT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1045898..1046200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 110350 RMVar_ID_110350 Human_SNP_ID_800593032 m1A Human chr1 - 35192248 35192248 35192248 AGGGGCCCCCGCCCGGCGGGCCCGGCGGCCGCAGCGAGGAGAAGATCTCGGACTCGGAGGTGAGT AGGGGCCCCCGCCCGGCGGGCCCGGCGGCCGCCGCGAGGAGAAGATCTCGGACTCGGAGGTGAGT T G SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:35192219..35192435 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_221383,Human_RBP_ID_803359,Human_RBP_ID_859595,Human_RBP_ID_4047425,Human_RBP_ID_5335218,Human_RBP_ID_9358595,Human_RBP_ID_10955216,Human_RBP_ID_19037614,Human_RBP_ID_22429231,Human_RBP_ID_26863467 Human_Splice_Rec_46335 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 110351 RMVar_ID_110351 Human_SNP_ID_800596814 m1A Human chr1 + 35641426 35641426 35641426 AACATAGTCGGGGCCTTGGATACCGATGAGGTACTCCATGGTGGCGGAAGGCCAGGGGCTGCAGG AACATAGTCGGGGCCTTGGATACCGATGAGGTTCTCCATGGTGGCGGAAGGCCAGGGGCTGCAGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:35641376..35641500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 1 haematopoietic and lymphoid tissue 110352 RMVar_ID_110352 Human_SNP_ID_800597417 m1A Human chr1 - 156593990 156593990 156593990 TCTCCAGAGCAGGTGGCACAAAACGACCCCCCAGGTAATGGTAGCGACCGGTAAACTGGGTTGCA TCTCCAGAGCAGGTGGCACAAAACGACCCCCCGGGTAATGGTAGCGACCGGTAAACTGGGTTGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156593939..156594062 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 110353 RMVar_ID_110353 Human_SNP_ID_800602149 m1A Human chr1 + 155268828 155268828 155268828 CTGTCGGGGGGCAGGGGGGGTCGGAGCAAGCCAGGTGTCGGAGCGGGGGCCGGAGGGAGGCGGGG CTGTCGGGGGGCAGGGGGGGTCGGAGCAAGCCGGGTGTCGGAGCGGGGGCCGGAGGGAGGCGGGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:155268778..155268925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 4 oesophagus 110354 RMVar_ID_110354 Human_SNP_ID_800604015 m1A Human chr1 - 45698302 45698302 45698302 ATATATTAAAGGTCTTGCATACAGTAAAAAAAATTTTTTTTTGAGATGGAATTTTGCTCTTGTTG ATATATTAAAGGTCTTGCATACAGTAAAAAAATTTTTTTTTTGAGATGGAATTTTGCTCTTGTTG T A IPP Ensembl:ENSG00000197429 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3014243 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_13248,GWAS_ID_13249,GWAS_ID_13250,GWAS_ID_13251,GWAS_ID_13252,GWAS_ID_13253,GWAS_ID_13254,GWAS_ID_13255,GWAS_ID_13256,GWAS_ID_13257,GWAS_ID_13258,GWAS_ID_13259,GWAS_ID_13260,GWAS_ID_13261,GWAS_ID_13262,GWAS_ID_13263,GWAS_ID_13264,GWAS_ID_13265,GWAS_ID_13266,GWAS_ID_13267,GWAS_ID_13268,GWAS_ID_13269,GWAS_ID_13270,GWAS_ID_13271,GWAS_ID_13272,GWAS_ID_13273,GWAS_ID_13274,GWAS_ID_13275,GWAS_ID_13276,GWAS_ID_13277,GWAS_ID_13278,GWAS_ID_13279,GWAS_ID_13280,GWAS_ID_13281,GWAS_ID_13282,GWAS_ID_13283,GWAS_ID_13284,GWAS_ID_13285,GWAS_ID_13286,GWAS_ID_13287,GWAS_ID_13288,GWAS_ID_13289,GWAS_ID_13290,GWAS_ID_13291,GWAS_ID_13292,GWAS_ID_13293,GWAS_ID_13294,GWAS_ID_13295,GWAS_ID_13296,GWAS_ID_13297,GWAS_ID_13298,GWAS_ID_13299,GWAS_ID_13300,GWAS_ID_13301,GWAS_ID_13302,GWAS_ID_13303,GWAS_ID_13304,GWAS_ID_13305,GWAS_ID_13306,GWAS_ID_13307,GWAS_ID_13308,GWAS_ID_13309,GWAS_ID_13310,GWAS_ID_13311,GWAS_ID_13312,GWAS_ID_13313,GWAS_ID_13314,GWAS_ID_13315,GWAS_ID_13316,GWAS_ID_13317,GWAS_ID_13318,GWAS_ID_13319,GWAS_ID_13320,GWAS_ID_13321,GWAS_ID_13322,GWAS_ID_13323,GWAS_ID_13324,GWAS_ID_13325,GWAS_ID_13326,GWAS_ID_13327,GWAS_ID_13328,GWAS_ID_13329,GWAS_ID_13330,GWAS_ID_13331,GWAS_ID_13332,GWAS_ID_13333,GWAS_ID_13334,GWAS_ID_13335,GWAS_ID_13336,GWAS_ID_13337,GWAS_ID_13338,GWAS_ID_13339,GWAS_ID_13340,GWAS_ID_13341,GWAS_ID_13342,GWAS_ID_13343,GWAS_ID_13344,GWAS_ID_13345,GWAS_ID_13346,GWAS_ID_13347,GWAS_ID_13348,GWAS_ID_13349,GWAS_ID_13350,GWAS_ID_13351,GWAS_ID_13352,GWAS_ID_13353,GWAS_ID_13354,GWAS_ID_13355,GWAS_ID_13356,GWAS_ID_13357,GWAS_ID_13358,GWAS_ID_13359,GWAS_ID_13360,GWAS_ID_13361,GWAS_ID_13362,GWAS_ID_13363,GWAS_ID_13364,GWAS_ID_13365,GWAS_ID_13366,GWAS_ID_13367,GWAS_ID_13368,GWAS_ID_13369,GWAS_ID_13370 110355 RMVar_ID_110355 Human_SNP_ID_800605231 m1A Human chr1 - 156055351 156055351 156055351 CGCTTGGTTCCCGTTCCGGTCGTAGGCGGCCCAGATGTTACTGGCTATGGCAGCGGTGACCCGGG CGCTTGGTTCCCGTTCCGGTCGTAGGCGGCCCTGATGTTACTGGCTATGGCAGCGGTGACCCGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156055223..156055384 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 110356 RMVar_ID_110356 Human_SNP_ID_800609985 m1A Human chr1 + 1273779 1273779 1273779 GCCCGCGCCCGAAACAGCCGCACCGCCCCGGGATTGGGCCCACCGAACCCGCCGCAGCGCCGCCG GCCCGCGCCCGAAACAGCCGCACCGCCCCGGGGTTGGGCCCACCGAACCCGCCGCAGCGCCGCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:1273651..1273850;chr1:1273134..1273850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 110357 RMVar_ID_110357 Human_SNP_ID_800613978 m1A Human chr1 + 162784703 162784702 162784703 CAGTGGGGAATTGTTGAGTTGCTGTATCCTTTAAAAAAAAACAAAAAACTTGTTATTTTGAAAGA CAGTGGGGAATTGTTGAGTTGCTGTATCCTTT_AAAAAAAACAAAAAACTTGTTATTTTGAAAGA TA T DDR2 Ensembl:ENSG00000162733 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs887936133 Functional Loss DEL ICGC 33..33 33 MELA 1 - Human_RBP_ID_17729106 110358 RMVar_ID_110358 Human_SNP_ID_800617959 m1A Human chr1 + 154970402 154970402 154970402 CGTCCCCAGGCAGAGGAGGCAGGATGGGCCCCAGGGATGAAGCTGATGGGGAAGGCAGCTCCTCC CGTCCCCAGGCAGAGGAGGCAGGATGGGCCCCGGGGATGAAGCTGATGGGGAAGGCAGCTCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154970394..154970750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110359 RMVar_ID_110359 Human_SNP_ID_800627123 m1A Human chr1 + 226965406 226965406 226965406 TAAGGCTCGCCCCGAGAACAAGCAGCACAAACAGACGGTGCGTATGGGAGGCCCCTGGAGGGCCG TAAGGCTCGCCCCGAGAACAAGCAGCACAAACTGACGGTGCGTATGGGAGGCCCCTGGAGGGCCG A T COQ8A Ensembl:ENSG00000163050 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:226965356..226965717 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 5 lung Human_RBP_ID_22750533 Human_Splice_Rec_193559,Human_Splice_Rec_193589,Human_Splice_Rec_193631,Human_Splice_Rec_193659 RMVar_hsa_circ_21257,RMVar_hsa_circ_99597,RMVar_hsa_circ_281105,RMVar_hsa_circ_140123,RMVar_hsa_circ_344409,RMVar_hsa_circ_140124 110360 RMVar_ID_110360 Human_SNP_ID_800628984 m1A Human chr1 - 31424761 31424761 31424761 CGTGGCGAAGCACATGCGGTAGACAGCGCGGTAGCCAAGCAGGGAGCCACAGTCGATGTGGCCCT CGTGGCGAAGCACATGCGGTAGACAGCGCGGTGGCCAAGCAGGGAGCCACAGTCGATGTGGCCCT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:31423832..31425387 26863410 MeRIP-seq:(Medium) rs782371695 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 110361 RMVar_ID_110361 Human_SNP_ID_800630528 m1A Human chr1 + 116397991 116397991 116397991 TGAAGTACCACACTGAGATAGTGTTTGCCAGGACCTCCCCTCAGCAGAAGCTCATCATTGTGGAA TGAAGTACCACACTGAGATAGTGTTTGCCAGGGCCTCCCCTCAGCAGAAGCTCATCATTGTGGAA A G ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:116397844..116398079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_22809,Human_RBP_ID_222845,Human_RBP_ID_857879,Human_RBP_ID_1409263,Human_RBP_ID_1723231,Human_RBP_ID_3278018,Human_RBP_ID_5677049,Human_RBP_ID_8282179,Human_RBP_ID_8733318,Human_RBP_ID_17329606,Human_RBP_ID_18548558,Human_RBP_ID_22428542,Human_RBP_ID_22749386,Human_RBP_ID_22779275,Human_RBP_ID_22845235,Human_RBP_ID_26838579 Human_Splice_Rec_113839,Human_Splice_Rec_113887,Human_Splice_Rec_113941 RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_135609,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_64344,RMVar_hsa_circ_20747,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_135618,RMVar_hsa_circ_135619,RMVar_hsa_circ_112954,RMVar_hsa_circ_69417,RMVar_hsa_circ_135621,RMVar_hsa_circ_109389,RMVar_hsa_circ_79272,RMVar_hsa_circ_135622,RMVar_hsa_circ_84579,RMVar_hsa_circ_135623,RMVar_hsa_circ_135625,RMVar_hsa_circ_135624,RMVar_hsa_circ_376249 110362 RMVar_ID_110362 Human_SNP_ID_800639970 m1A Human chr1 + 207752217 207752217 207752217 AGAAATAACAGCGTCTTCCGCGCCGCGCATGGAGCCTCCCGGCCGCCGCGAGTGTCCCTTTCCTT AGAAATAACAGCGTCTTCCGCGCCGCGCATGGTGCCTCCCGGCCGCCGCGAGTGTCCCTTTCCTT A T CD46 Ensembl:ENSG00000117335 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:207752176..207752275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 12 uterus Human_RBP_ID_742160,Human_RBP_ID_802967,Human_RBP_ID_4073251,Human_RBP_ID_5311958,Human_RBP_ID_9319342,Human_RBP_ID_22427777 Human_Splice_Rec_182843,Human_Splice_Rec_182867,Human_Splice_Rec_182893,Human_Splice_Rec_182915,Human_Splice_Rec_182933,Human_Splice_Rec_182955,Human_Splice_Rec_182975,Human_Splice_Rec_182999,Human_Splice_Rec_183027,Human_Splice_Rec_183043,Human_Splice_Rec_183061 Human_miRNA_ID_2895930 RMVar_hsa_circ_139303,RMVar_hsa_circ_139307,RMVar_hsa_circ_117588 110363 RMVar_ID_110363 Human_SNP_ID_800640085 m1A Human chr1 - 156243909 156243901 156243910 AGGGACCGTGAGGGGGCTCTTGATGGGAGTGGAAGAAGTGCTGAGGGTCTGAGAGGGGAGATGCA AGGGACCGTGAGGGGGCTCTTGATGGGAGTG_________CTGAGGGTCTGAGAGGGGAGATGCA GCACTTCTTC G PAQR6 Ensembl:ENSG00000160781 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156243858..156244090 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..40 33 LUAD 1 - Human_RBP_ID_1344998,Human_RBP_ID_10605751,Human_RBP_ID_21961516,Human_RBP_ID_22780558,Human_RBP_ID_23336226 110364 RMVar_ID_110364 Human_SNP_ID_800642701 m1A Human chr1 + 66925046 66925046 66925046 CCCGGCTGCAGGCGGATGGATGGGGCTTCTTCAGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG CCCGGCTGCAGGCGGATGGATGGGGCTTCTTCGGGCGGTGGCGGCAGCAGCGAAGGTGGCGGCGG A G MIER1 Ensembl:ENSG00000198160 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:66924874..66925165;chr1:66924960..66925175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_4074110,Human_RBP_ID_18968509 Human_Splice_Rec_83705,Human_Splice_Rec_83731,Human_Splice_Rec_83761,Human_Splice_Rec_83789,Human_Splice_Rec_83815,Human_Splice_Rec_83845,Human_Splice_Rec_83873 110365 RMVar_ID_110365 Human_SNP_ID_800648449 m1A Human chr1 + 2228759 2228759 2228759 CGCGCGGGAGCGGGAGCGGCCGGGGGAGCCGGAGCGCACCATGGAGGCGGCGGCAGGCGGCCGCG CGCGCGGGAGCGGGAGCGGCCGGGGGAGCCGGCGCGCACCATGGAGGCGGCGGCAGGCGGCCGCG A C SKI Ensembl:ENSG00000157933 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2228637..2228850;chr1:2228701..2229253 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_62,Human_RBP_ID_258751,Human_RBP_ID_3329493,Human_RBP_ID_3932544,Human_RBP_ID_4072446,Human_RBP_ID_5157956,Human_RBP_ID_5234213,Human_RBP_ID_5312210,Human_RBP_ID_5518321,Human_RBP_ID_8166299,Human_RBP_ID_8724773,Human_RBP_ID_9269552,Human_RBP_ID_9318461,Human_RBP_ID_9342474,Human_RBP_ID_9352350,Human_RBP_ID_17646234,Human_RBP_ID_17668058,Human_RBP_ID_18186762,Human_RBP_ID_18455365,Human_RBP_ID_18474698,Human_RBP_ID_22026214,Human_RBP_ID_22427995,Human_RBP_ID_22562015,Human_RBP_ID_22706506,Human_RBP_ID_22871552,Human_RBP_ID_26772916,Human_RBP_ID_27393901,Human_RBP_ID_27571500 110366 RMVar_ID_110366 Human_SNP_ID_800652484 m1A Human chr1 - 155330474 155330474 155330474 GCCAGTCCTCATCCACTGTGGTGATGACACGCAGCACTTCCCCACGCCGGAAGCTCAACTGGTCA GCCAGTCCTCATCCACTGTGGTGATGACACGCGGCACTTCCCCACGCCGGAAGCTCAACTGGTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155330426..155330600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 110367 RMVar_ID_110367 Human_SNP_ID_800656785 m1A Human chr1 - 234608681 234608681 234608681 CGCCGCCGCCTGCGCACCGGGGCCCGGCCGACAGCCTGTCCACCGCGGCCGGGGCCGCCGAGCTG CGCCGCCGCCTGCGCACCGGGGCCCGGCCGACGGCCTGTCCACCGCGGCCGGGGCCGCCGAGCTG T C IRF2BP2 Ensembl:ENSG00000168264 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:234608579..234608680 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_8755443,Human_RBP_ID_9270758,Human_RBP_ID_18187894 110368 RMVar_ID_110368 Human_SNP_ID_800656901 m1A Human chr1 + 39576550 39576550 39576550 GGGGAGGGCACGGCGGGCCGGGCGGGCGGCTCACCCCCGGACCGACGGACGGAGACCGACGGACG GGGGAGGGCACGGCGGGCCGGGCGGGCGGCTCCCCCCCGGACCGACGGACGGAGACCGACGGACG A C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:39576451..39576725 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110369 RMVar_ID_110369 Human_SNP_ID_800679030 m1A Human chr1 + 1817840 1817838 1817840 TGGCTCTGCGTGACTCAGTGGGCTCTTACCTGAGAGAGAGTTGCATCTGCACATGCTTTCCTGGC TGGCTCTGCGTGACTCAGTGGGCTCTTACCT__GAGAGAGTTGCATCTGCACATGCTTTCCTGGC TGA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:1817826..1817900 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 COAD,STAD 2 - 110370 RMVar_ID_110370 Human_SNP_ID_800684913 m1A Human chr1 - 154962469 154962469 154962469 CAGTTCCTGAGTACCTTCTACAGGCCCGGCCCAGCCTAGGCCCGGGGTGGCCACACCACAGCAAG CAGTTCCTGAGTACCTTCTACAGGCCCGGCCCGGCCTAGGCCCGGGGTGGCCACACCACAGCAAG T C SHC1,PYGO2 Ensembl:ENSG00000160691,Ensembl:ENSG00000163348 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:154962223..154962525;chr1:154962323..154962575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_327696,Human_RBP_ID_26386481 Human_miRNA_ID_2673919,Human_miRNA_ID_2673920,Human_miRNA_ID_2924675,Human_miRNA_ID_2924676 RMVar_hsa_circ_114089,RMVar_hsa_circ_93581,RMVar_hsa_circ_123316,RMVar_hsa_circ_136470,RMVar_hsa_circ_136472,RMVar_hsa_circ_91316,RMVar_hsa_circ_136473,RMVar_hsa_circ_136471 110371 RMVar_ID_110371 Human_SNP_ID_800687017 m1A Human chr1 + 64144013 64144013 64144013 GGAGATCAGTTGGGAAGCTACTGCAGGAATGCAGGGGAGAGATAAAGTGGCCTTGACAGGAGGAG GGAGATCAGTTGGGAAGCTACTGCAGGAATGCGGGGGAGAGATAAAGTGGCCTTGACAGGAGGAG A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:64143963..64144201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_363351 110372 RMVar_ID_110372 Human_SNP_ID_800688602 m1A Human chr1 - 203047192 203047192 203047192 GTCCTGGGTCTGCTGGGACACAGCCAGGCTGCAGGTTCCGTCCTCGAAGCAGCTGAGCTGCACAC GTCCTGGGTCTGCTGGGACACAGCCAGGCTGCGGGTTCCGTCCTCGAAGCAGCTGAGCTGCACAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:203039147..203049752 32194978 MeRIP-seq:(Medium) rs114629482 Functional Loss SNV ICGC 33..33 33 LAML 1 - 110373 RMVar_ID_110373 Human_SNP_ID_800694488 m1A Human chr1 - 220094301 220094301 220094301 CCTCTTCGTCGCCCCTTGCCATCCCGGGCTGCAGGGAAGGCGGGGCGTCCCCCACAAACTTCGGG CCTCTTCGTCGCCCCTTGCCATCCCGGGCTGCGGGGAAGGCGGGGCGTCCCCCACAAACTTCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:220094200..220094300 32194978 MeRIP-seq:(Medium) rs1167991391 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 110374 RMVar_ID_110374 Human_SNP_ID_800701659 m1A Human chr1 - 24745523 24745523 24745523 ATGGCCGGCTCGGCTGCGCTCCGCGAACGGCGAGGGCTGCTGCTGCTGCTGCTGCTTCTGCTCCG ATGGCCGGCTCGGCTGCGCTCCGCGAACGGCGGGGGCTGCTGCTGCTGCTGCTGCTTCTGCTCCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:24745426..24745600 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 110375 RMVar_ID_110375 Human_SNP_ID_800718539 m1A Human chr1 - 790461 790461 790461 TCGAGTCCATTCCATTCCATTCCATCTGAGTCAATTCCATTCCATTCCATTCGAGTCCATTCCAT TCGAGTCCATTCCATTCCATTCCATCTGAGTCCATTCCATTCCATTCCATTCGAGTCCATTCCAT T G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:790429..790689 26863196 MeRIP-seq:(Medium) rs111203401 Functional Loss SNV ICGC 33..33 33 COCA 1 - 110376 RMVar_ID_110376 Human_SNP_ID_800722190 m1A Human chr1 - 233614136 233614136 233614136 CTCCACCGCCGCCGCCAAGGCCAACGCCGCAGACCGGCCGGAGCGCGGCCCGCCGCCTCTTCTGG CTCCACCGCCGCCGCCAAGGCCAACGCCGCAGGCCGGCCGGAGCGCGGCCCGCCGCCTCTTCTGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:233614003..233614274 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 110377 RMVar_ID_110377 Human_SNP_ID_800735832 m1A Human chr1 + 156325067 156325067 156325067 GTTGGGTGCATCTGCTGCTCCAGGAAGTGCTCAGCTACAGACAGCATTTCCCCTGCTGAAAAAGA GTTGGGTGCATCTGCTGCTCCAGGAAGTGCTCGGCTACAGACAGCATTTCCCCTGCTGAAAAAGA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156324951..156325100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney 110378 RMVar_ID_110378 Human_SNP_ID_800751457 m1A Human chr1 - 953259 953259 953259 CAGAGAATGGTGATCGTATGGAGCACTGGGGAAGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT CAGAGAATGGTGATCGTATGGAGCACTGGGGAGGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT T C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3748596 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 6 head and neck Human_RBP_ID_223048,Human_RBP_ID_8754549,Human_RBP_ID_18966604 Human_Splice_Rec_1068,Human_Splice_Rec_1069,Human_Splice_Rec_1108,Human_Splice_Rec_1109 Human_miRNA_ID_2255883 GWAS_ID_7967,GWAS_ID_7968 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243 110379 RMVar_ID_110379 Human_SNP_ID_800753944 m1A Human chr1 + 218285384 218285384 218285384 GGAAGAAAACCTGAAAAAGACCCCAAAGAAGAAGATGAAAATGGTAACTGGAGCCGTAGCGTCGG GGAAGAAAACCTGAAAAAGACCCCAAAGAAGATGATGAAAATGGTAACTGGAGCCGTAGCGTCGG A T RRP15 Ensembl:ENSG00000067533 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:218285355..218285559 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_24172,Human_RBP_ID_9357521,Human_RBP_ID_23112607,Human_RBP_ID_26312706,Human_RBP_ID_26852775 Human_Splice_Rec_188363,Human_Splice_Rec_188371 110380 RMVar_ID_110380 Human_SNP_ID_800766839 m1A Human chr1 - 11858870 11858870 11858870 CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGAAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG CGGACGCATCGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCCTCCGCAGTCCCTCCAG T G NPPB Ensembl:ENSG00000120937 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11858823..11858922 26863196 MeRIP-seq:(Medium) rs1000622449 Functional Loss SNV ICGC,COSMIC 33..33 33 MELA,eye mixed 2 eye 110381 RMVar_ID_110381 Human_SNP_ID_800778862 m1A Human chr1 - 6197752 6197751 6197752 CTCTGTTATCATTTGTGTATTTTCTTAGAAAAAGCTTGTGGTGAAGGGGGGCAAAAAAAAGAAGC CTCTGTTATCATTTGTGTATTTTCTTAGAAAA_GCTTGTGGTGAAGGGGGGCAAAAAAAAGAAGC CT C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:6197701..6197775 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 STAD,LIHC,KIRP 3 - Human_RBP_ID_24279,Human_RBP_ID_359496,Human_RBP_ID_744618,Human_RBP_ID_1433366,Human_RBP_ID_1751953,Human_RBP_ID_3319004,Human_RBP_ID_17454149,Human_RBP_ID_17646832,Human_RBP_ID_18578920,Human_RBP_ID_22025813,Human_RBP_ID_23406163,Human_RBP_ID_24717620,Human_RBP_ID_26309619 Human_Splice_Rec_11626,Human_Splice_Rec_11636,Human_Splice_Rec_11644,Human_Splice_Rec_11656,Human_Splice_Rec_11664 RMVar_hsa_circ_29294,RMVar_hsa_circ_300295,RMVar_hsa_circ_337176 110382 RMVar_ID_110382 Human_SNP_ID_800788470 m1A Human chr1 + 173865478 173865466 173865479 ACGTTAACATCAATAAAACATGTACCTTTAAAAGGTATGACAGGAACTGTCTTCATGTCCTTACC ACGTTAACATCAATAAAACAT_____________GTATGACAGGAACTGTCTTCATGTCCTTACC TGTACCTTTAAAAG T lnc-ZBTB37-2 RNACentral:URS00008B82B3 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:173865476..173865525 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 22..34 33 NKTL 1 - 110383 RMVar_ID_110383 Human_SNP_ID_800789135 m1A Human chr1 - 207322387 207322387 207322387 CTGGGCATTAGGTACATCTGGGGGAAGGCCACAGTCACCTAGGGAGACAAAAGCAGAACTGAAGG CTGGGCATTAGGTACATCTGGGGGAAGGCCACGGTCACCTAGGGAGACAAAAGCAGAACTGAAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:207322376..207322400 26863196 MeRIP-seq:(Medium) rs1261776205 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma,stomach adenocarcinoma 14 stomach 110384 RMVar_ID_110384 Human_SNP_ID_800811015 m1A Human chr1 - 85540252 85540252 85540252 AACATAAAGAGGAAGATAGGGAAATAAGACTAAAAGGTGTAACCCCAGGTCAAAGGAAAAGGGAA AACATAAAGAGGAAGATAGGGAAATAAGACTAGAAGGTGTAACCCCAGGTCAAAGGAAAAGGGAA T C DDAH1,AC092807.4 Ensembl:ENSG00000153904,Ensembl:ENSG00000282057 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:85540249..85540412 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_93310,RMVar_hsa_circ_134294 110385 RMVar_ID_110385 Human_SNP_ID_800827534 m1A Human chr1 - 43592469 43592469 43592469 GTCCTCTAGTGTGTAGGAGGAGGTTGGGTCGAAGGTCACCTTGTGCTGGGAAGAGCAGGGAGCAC GTCCTCTAGTGTGTAGGAGGAGGTTGGGTCGAGGGTCACCTTGTGCTGGGAAGAGCAGGGAGCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43592451..43592575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 mouth squamous_cell_carcinoma,HNSC,head_neck squamous_cell_carcinoma 6 head and neck 110386 RMVar_ID_110386 Human_SNP_ID_800845373 m1A Human chr1 + 76700050 76700050 76700050 GGGAGATCAGCCCTGGCATGATCAAAGACTGCAGAGCCACGTGGGTGGTCCTGGGGCACTCAGAG GGGAGATCAGCCCTGGCATGATCAAAGACTGCGGAGCCACGTGGGTGGTCCTGGGGCACTCAGAG A G TPI1P1 Ensembl:ENSG00000226415 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs542567612 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5156203,Human_RBP_ID_17456893,Human_RBP_ID_26391190 Human_miRNA_ID_1855418,Human_miRNA_ID_1908254 110387 RMVar_ID_110387 Human_SNP_ID_800854321 m1A Human chr1 + 43883197 43883197 43883197 CAGTGTGTTGCCTAGGCTGGTCTCAAACTCCTAGGTTCAAACAGTTCTCCCACCTCAGCCTTCTA CAGTGTGTTGCCTAGGCTGGTCTCAAACTCCTTGGTTCAAACAGTTCTCCCACCTCAGCCTTCTA A T AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:43883188..43883315 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 33 liver RMVar_hsa_circ_5322,RMVar_hsa_circ_40460,RMVar_hsa_circ_8358,RMVar_hsa_circ_77089,RMVar_hsa_circ_132337,RMVar_hsa_circ_321076,RMVar_hsa_circ_375524,RMVar_hsa_circ_48260,RMVar_hsa_circ_7537,RMVar_hsa_circ_132340,RMVar_hsa_circ_51949 110388 RMVar_ID_110388 Human_SNP_ID_800858264 m1A Human chr1 - 8874902 8874902 8874902 GTGTGTTTCTTCTACAGAAGTTCACCATGTCTATTCTCAAGATCCATGCCAGGGAGATCTTTGAC GTGTGTTTCTTCTACAGAAGTTCACCATGTCTGTTCTCAAGATCCATGCCAGGGAGATCTTTGAC T C ENO1 Ensembl:ENSG00000074800 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8874851..8874979 26863196 MeRIP-seq:(Medium) rs759744149 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_858388,Human_RBP_ID_1156312,Human_RBP_ID_1350027,Human_RBP_ID_1436524,Human_RBP_ID_1756045,Human_RBP_ID_2171287,Human_RBP_ID_3324880,Human_RBP_ID_4075084,Human_RBP_ID_8321125,Human_RBP_ID_8752670,Human_RBP_ID_9318554,Human_RBP_ID_17220428,Human_RBP_ID_17760043,Human_RBP_ID_18186808,Human_RBP_ID_18582612,Human_RBP_ID_19451569,Human_RBP_ID_23150762,Human_RBP_ID_23418802,Human_RBP_ID_24454667,Human_RBP_ID_24736071,Human_RBP_ID_26797623 Human_Splice_Rec_14264,Human_Splice_Rec_14265,Human_Splice_Rec_14302,Human_Splice_Rec_14303,Human_Splice_Rec_14324,Human_Splice_Rec_14325,Human_Splice_Rec_14348,Human_Splice_Rec_14349,Human_Splice_Rec_14376,Human_Splice_Rec_14377,Human_Splice_Rec_14388,Human_Splice_Rec_14389,Human_Splice_Rec_14400,Human_Splice_Rec_14401,Human_Splice_Rec_14410,Human_Splice_Rec_14411,Human_Splice_Rec_14420,Human_Splice_Rec_14421,Human_Splice_Rec_14432,Human_Splice_Rec_14433,Human_Splice_Rec_14440,Human_Splice_Rec_14441,Human_Splice_Rec_14448,Human_Splice_Rec_14449,Human_Splice_Rec_14454,Human_Splice_Rec_14455 Human_miRNA_ID_2491892,Human_miRNA_ID_2864406,Human_miRNA_ID_2917584 RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128753,RMVar_hsa_circ_128752,RMVar_hsa_circ_124829,RMVar_hsa_circ_128776,RMVar_hsa_circ_128782,RMVar_hsa_circ_128778,RMVar_hsa_circ_376211,RMVar_hsa_circ_76772,RMVar_hsa_circ_93328,RMVar_hsa_circ_128783,RMVar_hsa_circ_119235,RMVar_hsa_circ_128009,RMVar_hsa_circ_128789,RMVar_hsa_circ_118160,RMVar_hsa_circ_112445,RMVar_hsa_circ_128791,RMVar_hsa_circ_128792,RMVar_hsa_circ_128794,RMVar_hsa_circ_81682,RMVar_hsa_circ_128793 110389 RMVar_ID_110389 Human_SNP_ID_800869544 m1A Human chr1 - 93847599 93847599 93847599 ACCTTTGAATGCCTTCAGCCTCTAGAAGTCCAATGCGCTATCCATTGCGCCACGGAGCCACCTGT ACCTTTGAATGCCTTCAGCCTCTAGAAGTCCACTGCGCTATCCATTGCGCCACGGAGCCACCTGT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:93847447..93847729 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 110390 RMVar_ID_110390 Human_SNP_ID_800874699 m1A Human chr1 - 148532727 148532727 148532727 TTTTAATTTGAACCACGTATCTCTGGGTAGCTACAAAATTCCTCAGGGATTTCATTTTGCAGGCA TTTTAATTTGAACCACGTATCTCTGGGTAGCTGCAAAATTCCTCAGGGATTTCATTTTGCAGGCA T C NBPF14 Ensembl:ENSG00000270629 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1329712810 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110391 RMVar_ID_110391 Human_SNP_ID_800881890 m1A Human chr1 - 43164492 43164492 43164492 GTGACCAGATGTGGTATGTCTTTTTCTGTAGAAGAGACCTGGAAAACGAACAAGAGAGAAGATGA GTGACCAGATGTGGTATGTCTTTTTCTGTAGAGGAGACCTGGAAAACGAACAAGAGAGAAGATGA T C EBNA1BP2 Ensembl:ENSG00000117395 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:43164451..43164500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_1438140,Human_RBP_ID_2148598,Human_RBP_ID_26311098 Human_Splice_Rec_57086,Human_Splice_Rec_57102,Human_Splice_Rec_57112 110392 RMVar_ID_110392 Human_SNP_ID_800918570 m1A Human chr1 + 35641447 35641447 35641447 ACCGATGAGGTACTCCATGGTGGCGGAAGGCCAGGGGCTGCAGGTCCGACACAGCACGAGACTCG ACCGATGAGGTACTCCATGGTGGCGGAAGGCCTGGGGCTGCAGGTCCGACACAGCACGAGACTCG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:35641401..35641525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 110393 RMVar_ID_110393 Human_SNP_ID_800920715 m1A Human chr1 - 121184136 121184136 121184136 TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCAAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG TGAGGGAAGGGAGGACGCGAGAGAAACAGCGCGAGCACGCTGAGGGCCGGGGGTTGCCAGGAGAG T C FAM72B Ensembl:ENSG00000188610 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:121183915..121184200;chr1:121183907..121184200;chr1:121183930..121184200 26863196 MeRIP-seq:(Medium) rs1172651974 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue NK-T_cell_lymphoma 8 haematopoietic and lymphoid tissue Human_Splice_Rec_116697 110394 RMVar_ID_110394 Human_SNP_ID_800932859 m1A Human chr1 - 149914181 149914181 149914181 CTTTTGCTGTCTGTTATTTTTTCTAGGTCTCCAGAGGCTTGTGGAAGAGAAGCAGGCGACCCTTC CTTTTGCTGTCTGTTATTTTTTCTAGGTCTCCTGAGGCTTGTGGAAGAGAAGCAGGCGACCCTTC T A SV2A Ensembl:ENSG00000159164 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:149914101..149914242 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3991125 Human_Splice_Rec_125264,Human_Splice_Rec_125288 110395 RMVar_ID_110395 Human_SNP_ID_800945499 m1A Human chr1 - 156673020 156673020 156673020 AGGCCCGTACCCCTACCTTGGCCAGCACCCCCATCCCCCCCACACCTCAGGCACCCTCTCCTGCT AGGCCCGTACCCCTACCTTGGCCAGCACCCCCGTCCCCCCCACACCTCAGGCACCCTCTCCTGCT T C NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156673018..156673172 26863196 MeRIP-seq:(Medium) rs772195958 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_803587 Human_miRNA_ID_2652858,Human_miRNA_ID_2754053 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 110396 RMVar_ID_110396 Human_SNP_ID_800947110 m1A Human chr1 - 1349351 1349351 1349351 TTTAACGGCGCGGCCCGAGGGGCGCAGGCGGGAGGGCGGCGGGGCTGAGCGCGCCCTCCGTGCTG TTTAACGGCGCGGCCCGAGGGGCGCAGGCGGGGGGGCGGCGGGGCTGAGCGCGCCCTCCGTGCTG T C DVL1 Ensembl:ENSG00000107404 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1342717..1349400 26863196 MeRIP-seq:(Medium) rs1004676729 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110397 RMVar_ID_110397 Human_SNP_ID_800949275 m1A Human chr1 + 227734869 227734869 227734869 CATGCCATCTCCCTGGGCCCCGTCCTCACTCCAAACCGTCTGCAGAGGAACTCTCCAGGGGCCAC CATGCCATCTCCCTGGGCCCCGTCCTCACTCCGAACCGTCTGCAGAGGAACTCTCCAGGGGCCAC A G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:227734848..227734979 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 face Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 5 skin,head and neck 110398 RMVar_ID_110398 Human_SNP_ID_800960846 m1A Human chr1 - 156480931 156480931 156480931 GAAGAAGGGCTTCAACGGCTGCGACAGCCCCGAGCCCGACGGGGAGGACTCGCTGGAACAGAGCC GAAGAAGGGCTTCAACGGCTGCGACAGCCCCGGGCCCGACGGGGAGGACTCGCTGGAACAGAGCC T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156480770..156482492 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_221412,Human_RBP_ID_859880,Human_RBP_ID_18969150 Human_Splice_Rec_142868,Human_Splice_Rec_142869,Human_Splice_Rec_142890,Human_Splice_Rec_142891,Human_Splice_Rec_142910,Human_Splice_Rec_142911,Human_Splice_Rec_142926,Human_Splice_Rec_142927 RMVar_hsa_circ_22376,RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846,RMVar_hsa_circ_343418,RMVar_hsa_circ_94677,RMVar_hsa_circ_136849,RMVar_hsa_circ_7432 110399 RMVar_ID_110399 Human_SNP_ID_800962490 m1A Human chr1 - 92837551 92837551 92837551 AAGCATCTTCATCTTCTTCCATTAAGTAGCGCATGTAATCTGCAACATTCTGGCCCATGATGTGC AAGCATCTTCATCTTCTTCCATTAAGTAGCGCGTGTAATCTGCAACATTCTGGCCCATGATGTGC T C DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:92837451..92841925 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 12 stomach 110400 RMVar_ID_110400 Human_SNP_ID_800963881 m1A Human chr1 - 244862732 244862732 244862732 GGCTTGGCCTTTATGGGGCTCGTGTGTGTTTTAGGGGACGGCAAAACAGAACAGAAAGGCGGAGA GGCTTGGCCTTTATGGGGCTCGTGTGTGTTTTTGGGGACGGCAAAACAGAACAGAAAGGCGGAGA T A HNRNPU Ensembl:ENSG00000153187 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244862651..244862752 26863196 MeRIP-seq:(Medium) rs1411752390 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_349232,Human_RBP_ID_745159,Human_RBP_ID_1347750,Human_RBP_ID_4038810,Human_RBP_ID_5797449,Human_RBP_ID_10884133,Human_RBP_ID_17102550,Human_RBP_ID_22019682,Human_RBP_ID_22139583,Human_RBP_ID_22535742,Human_RBP_ID_22860729,Human_RBP_ID_23380421,Human_RBP_ID_24762836,Human_RBP_ID_26859435,Human_RBP_ID_27592033 110401 RMVar_ID_110401 Human_SNP_ID_800967196 m1A Human chr1 + 167789547 167789547 167789547 TAAAACAGGATTGAGATTTTGAGGTGTGCACAAGGTGGTAAGATAAAGGGCATATGAGCTTCAAA TAAAACAGGATTGAGATTTTGAGGTGTGCACAGGGTGGTAAGATAAAGGGCATATGAGCTTCAAA A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs3752606 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_13389,GWAS_ID_13390,GWAS_ID_13391,GWAS_ID_13392,GWAS_ID_13393,GWAS_ID_13394,GWAS_ID_13395,GWAS_ID_13396 110402 RMVar_ID_110402 Human_SNP_ID_800967706 m1A Human chr1 + 71868745 71868745 71868745 ATTTCTGAAACACACTTCTACTCCTTCCTCTCACTTATGTCTGCACTTTATATTCCTTCTTTCCT ATTTCTGAAACACACTTCTACTCCTTCCTCTCTCTTATGTCTGCACTTTATATTCCTTCTTTCCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:71868732..71868818 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 110403 RMVar_ID_110403 Human_SNP_ID_800969823 m1A Human chr1 + 70205530 70205530 70205530 CAGCGCGGAGATCCTGCCCCGCTATCCGCTTCAGGCGCGACATGTTCAAAGTCCTAGGTCCAGAA CAGCGCGGAGATCCTGCCCCGCTATCCGCTTCGGGCGCGACATGTTCAAAGTCCTAGGTCCAGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:70205423..70205534 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 110404 RMVar_ID_110404 Human_SNP_ID_800972333 m1A Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGGTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:214390976..214391050 26863196 MeRIP-seq:(Medium) rs7550799 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_RBP_ID_222385,Human_RBP_ID_17224160,Human_RBP_ID_19035924 Human_Splice_Rec_187330,Human_Splice_Rec_187331,Human_Splice_Rec_187364,Human_Splice_Rec_187365 GWAS_ID_5113 RMVar_hsa_circ_28179,RMVar_hsa_circ_83741,RMVar_hsa_circ_369866,RMVar_hsa_circ_266872,RMVar_hsa_circ_89481,RMVar_hsa_circ_102502,RMVar_hsa_circ_139564,RMVar_hsa_circ_139565,RMVar_hsa_circ_99604,RMVar_hsa_circ_101562,RMVar_hsa_circ_139567,RMVar_hsa_circ_139568,RMVar_hsa_circ_369918,RMVar_hsa_circ_139566,RMVar_hsa_circ_284728,RMVar_hsa_circ_92743,RMVar_hsa_circ_139570,RMVar_hsa_circ_139571,RMVar_hsa_circ_139572,RMVar_hsa_circ_139569 110405 RMVar_ID_110405 Human_SNP_ID_800973043 m1A Human chr1 + 19169486 19169484 19169486 AATTCATTGGTATTGATGTTGTTCCAGGACTCACACACAGTCTGCACTGACGATGGCAAATTCTG AATTCATTGGTATTGATGTTGTTCCAGGACT__CACACAGTCTGCACTGACGATGGCAAATTCTG TCA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19167163..19170788 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 COAD 1 - 110406 RMVar_ID_110406 Human_SNP_ID_800978862 m1A Human chr1 + 77942154 77942154 77942154 GAAGAAGAAGAACAAAGAAGAATTGAAGAACAAAAGTTACTACGCATGCAGTTTGAACAAAGGGA GAAGAAGAAGAACAAAGAAGAATTGAAGAACACAAGTTACTACGCATGCAGTTTGAACAAAGGGA A C NEXN Ensembl:ENSG00000162614 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:77942033..77942567 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_88863,Human_Splice_Rec_88887,Human_Splice_Rec_88921,Human_Splice_Rec_88937,Human_Splice_Rec_88939 RMVar_hsa_circ_134154,RMVar_hsa_circ_81737 110407 RMVar_ID_110407 Human_SNP_ID_801026798 m1A Human chr1 + 94530467 94530467 94530467 TGCAGTAGCTCCAACAGTGCTTCCTTTATGAAACATTCAGTGGGGAGTTCTCCTTCCAGCTCTGC TGCAGTAGCTCCAACAGTGCTTCCTTTATGAAGCATTCAGTGGGGAGTTCTCCTTCCAGCTCTGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:94530420..94530498 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 110408 RMVar_ID_110408 Human_SNP_ID_801026940 m1A Human chr1 - 44255362 44255362 44255362 GCTAGGAAAACTGAGTAGAGTGTCAAGAAGGGAGAAGGGTTTCAGAGATGGAGCAGGCTGCAAAA GCTAGGAAAACTGAGTAGAGTGTCAAGAAGGGTGAAGGGTTTCAGAGATGGAGCAGGCTGCAAAA T A ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:44255348..44255479;chr1:44255261..44255390 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_100254,RMVar_hsa_circ_132377,RMVar_hsa_circ_286708,RMVar_hsa_circ_292598,RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_24981,RMVar_hsa_circ_132380,RMVar_hsa_circ_132379 110409 RMVar_ID_110409 Human_SNP_ID_801039626 m1A Human chr1 + 236897756 236897756 236897756 ACAAAAAACCTGTGTGCATCTGGCTGACACTTACCTGCTTCTGGTTTTCGAAGACTATTTAGTGG ACAAAAAACCTGTGTGCATCTGGCTGACACTTCCCTGCTTCTGGTTTTCGAAGACTATTTAGTGG A C MTR Ensembl:ENSG00000116984 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2853522 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8746208,Human_RBP_ID_10864143,Human_RBP_ID_26377365,Human_RBP_ID_27178852 Human_miRNA_ID_821712 Clinvar_Rec_459,Clinvar_Rec_460,Clinvar_Rec_461,Clinvar_Rec_462 GWAS_ID_10550,GWAS_ID_10551,GWAS_ID_10552,GWAS_ID_10553,GWAS_ID_10554,GWAS_ID_10555,GWAS_ID_10556,GWAS_ID_10557,GWAS_ID_10558,GWAS_ID_10559,GWAS_ID_10560,GWAS_ID_10561,GWAS_ID_10562,GWAS_ID_10563,GWAS_ID_10564,GWAS_ID_10565,GWAS_ID_10566,GWAS_ID_10567,GWAS_ID_10568,GWAS_ID_10569,GWAS_ID_10570,GWAS_ID_10571,GWAS_ID_10572,GWAS_ID_10573,GWAS_ID_10574,GWAS_ID_10575,GWAS_ID_10576,GWAS_ID_10577,GWAS_ID_10578,GWAS_ID_10579,GWAS_ID_10580,GWAS_ID_10581,GWAS_ID_10582,GWAS_ID_10583,GWAS_ID_10584,GWAS_ID_10585,GWAS_ID_10586,GWAS_ID_10587,GWAS_ID_10588,GWAS_ID_10589,GWAS_ID_10590,GWAS_ID_10591,GWAS_ID_10592,GWAS_ID_10593,GWAS_ID_10594,GWAS_ID_10595,GWAS_ID_10596 110410 RMVar_ID_110410 Human_SNP_ID_801054870 m1A Human chr1 + 153936651 153936651 153936651 AGGGTGCCGACCGCACATAGGCAGGCAGACACAGGAACCACAGCCCATAGCAGTGCCCCAGCAGG AGGGTGCCGACCGCACATAGGCAGGCAGACACGGGAACCACAGCCCATAGCAGTGCCCCAGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:153936602..153937542 32194978 MeRIP-seq:(Medium) rs754098427 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110411 RMVar_ID_110411 Human_SNP_ID_801057608 m1A Human chr1 - 229271247 229271247 229271247 GCGTCTCGGTGGGGAAGGACCTGGGGCGGGGGACCGGAGGAGGGAGGGGCCCGACCGGTCCCCAC GCGTCTCGGTGGGGAAGGACCTGGGGCGGGGGGCCGGAGGAGGGAGGGGCCCGACCGGTCCCCAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:229271151..229271350 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110412 RMVar_ID_110412 Human_SNP_ID_801078832 m1A Human chr1 - 156743856 156743851 156743856 TCCTGCCTAGGACTCTCCTAAACGTCCCAAGGAGGCAGAAAACCCTGAAGGAGAGGAGAAGGAGG TCCTGCCTAGGACTCTCCTAAACGTCCCAAGG_____GAAAACCCTGAAGGAGAGGAGAAGGAGG CTGCCT C HDGF Ensembl:ENSG00000143321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:156743609..156743909;chr1:156743851..156743900 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..37 33 HNSC 1 - Human_RBP_ID_20978,Human_RBP_ID_855416,Human_RBP_ID_971825,Human_RBP_ID_1727101,Human_RBP_ID_3934185,Human_RBP_ID_5136886,Human_RBP_ID_8170769,Human_RBP_ID_9357043,Human_RBP_ID_18966127,Human_RBP_ID_22486143,Human_RBP_ID_22637662,Human_RBP_ID_26314844,Human_RBP_ID_26386574 Human_Splice_Rec_143606,Human_Splice_Rec_143616,Human_Splice_Rec_143626,Human_Splice_Rec_143640,Human_Splice_Rec_143650,Human_Splice_Rec_143654,Human_Splice_Rec_143662,Human_Splice_Rec_143674,Human_Splice_Rec_143684,Human_Splice_Rec_143690 RMVar_hsa_circ_82179,RMVar_hsa_circ_117608,RMVar_hsa_circ_108690,RMVar_hsa_circ_115770,RMVar_hsa_circ_99168,RMVar_hsa_circ_62751,RMVar_hsa_circ_136902,RMVar_hsa_circ_136904,RMVar_hsa_circ_136905,RMVar_hsa_circ_136903,RMVar_hsa_circ_136901,RMVar_hsa_circ_361976,RMVar_hsa_circ_363631,RMVar_hsa_circ_65078 110413 RMVar_ID_110413 Human_SNP_ID_801089034 m1A Human chr1 - 1487895 1487895 1487895 TAGTGACACTCACAGTGGCTCGCTTCCGAAGGAAGGCGTCTGCTTCATCCATGAAGAGCAGGAGG TAGTGACACTCACAGTGGCTCGCTTCCGAAGGGAGGCGTCTGCTTCATCCATGAAGAGCAGGAGG T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:1486611..1487906 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue 110414 RMVar_ID_110414 Human_SNP_ID_801090412 m1A Human chr1 - 44405421 44405421 44405421 AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCAGCGGCAGCAGC AAAAGTCCCGGGTTCGCAGAGCCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:44405382..44405512 26863196 MeRIP-seq:(Medium) rs1469380464 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 110415 RMVar_ID_110415 Human_SNP_ID_801090802 m1A Human chr1 - 3739314 3739314 3739314 GTTAGATAGAGGTCATCAGCTGGGTTGATTGTATGGGTTAGATAGAGGTCATCAGCTGGGTTGAT GTTAGATAGAGGTCATCAGCTGGGTTGATTGTGTGGGTTAGATAGAGGTCATCAGCTGGGTTGAT T C TP73-AS1 Ensembl:ENSG00000227372 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:3739208..3739350;chr1:3739144..3739375 26863196 MeRIP-seq:(Medium) rs375473604 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_353968,Human_RBP_ID_3332641,Human_RBP_ID_5086360,Human_RBP_ID_8171225,Human_RBP_ID_9412744,Human_RBP_ID_22369495,Human_RBP_ID_23263260,Human_RBP_ID_23391778,Human_RBP_ID_24358392 Human_Splice_Rec_9468,Human_Splice_Rec_9476 110416 RMVar_ID_110416 Human_SNP_ID_801091469 m1A Human chr1 + 70250473 70250473 70250473 AAGAAGAGTAAAGATAAGGAAAAGGACCGGGAAAGAAAATCAGAGAGTGATAAAGATGTAAAAGT AAGAAGAGTAAAGATAAGGAAAAGGACCGGGAGAGAAAATCAGAGAGTGATAAAGATGTAAAAGT A G SRSF11 Ensembl:ENSG00000116754 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:70250340..70250758 26863196 MeRIP-seq:(Medium) rs757016269 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck Human_RBP_ID_24354,Human_RBP_ID_223708,Human_RBP_ID_854856,Human_RBP_ID_1438160,Human_RBP_ID_1753513,Human_RBP_ID_2183989,Human_RBP_ID_3933633,Human_RBP_ID_5519065,Human_RBP_ID_5538024,Human_RBP_ID_5860168,Human_RBP_ID_8228018,Human_RBP_ID_8974059,Human_RBP_ID_9356478,Human_RBP_ID_11095863,Human_RBP_ID_17646462,Human_RBP_ID_18410181,Human_RBP_ID_22350482,Human_RBP_ID_22871808,Human_RBP_ID_23112426,Human_RBP_ID_23410942,Human_RBP_ID_24541153,Human_RBP_ID_24550371,Human_RBP_ID_26311431 Human_Splice_Rec_85203,Human_Splice_Rec_85231,Human_Splice_Rec_85315,Human_Splice_Rec_85333,Human_Splice_Rec_85347,Human_Splice_Rec_85353,Human_Splice_Rec_85355,Human_Splice_Rec_85359 RMVar_hsa_circ_56822,RMVar_hsa_circ_57402,RMVar_hsa_circ_316622,RMVar_hsa_circ_363422 110417 RMVar_ID_110417 Human_SNP_ID_801112139 m1A Human chr1 - 23559140 23559140 23559140 CGAGCCAGCCCCTGGACCCCCTGATGGCCCCCACCTTCCCATCCAGGTAAGCCTCGAAGTCGGGA CGAGCCAGCCCCTGGACCCCCTGATGGCCCCCGCCTTCCCATCCAGGTAAGCCTCGAAGTCGGGA T C ID3 Ensembl:ENSG00000117318 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:23558926..23559231 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_742156,Human_RBP_ID_858626,Human_RBP_ID_9358359,Human_RBP_ID_19034255,Human_RBP_ID_22426991,Human_RBP_ID_22750860,Human_RBP_ID_27835111 Human_Splice_Rec_30237,Human_Splice_Rec_30243 RMVar_hsa_circ_124280,RMVar_hsa_circ_130477 110418 RMVar_ID_110418 Human_SNP_ID_801115932 m1A Human chr1 + 119622391 119622391 119622391 TAGTCTATTGCCCGCCATCCTGTTCCCACCCCAGCCCACGAACTGCCCTTCCTCAAAGTGCCTGG TAGTCTATTGCCCGCCATCCTGTTCCCACCCCGGCCCACGAACTGCCCTTCCTCAAAGTGCCTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119622342..119622554 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 110419 RMVar_ID_110419 Human_SNP_ID_801118224 m1A Human chr1 - 224418261 224418261 224418261 CTGTGTCTCTGCTTATAGACCATGTTTGTAGTAGGTAAGAGGAAAACTTCCTATATTCTGAAACA CTGTGTCTCTGCTTATAGACCATGTTTGTAGTGGGTAAGAGGAAAACTTCCTATATTCTGAAACA T C WDR26 Ensembl:ENSG00000162923 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:224418250..224418375 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_851971,Human_RBP_ID_1737813,Human_RBP_ID_17222049,Human_RBP_ID_18564042,Human_RBP_ID_19040259 Human_Splice_Rec_191469,Human_Splice_Rec_191495,Human_Splice_Rec_191537,Human_Splice_Rec_191573 RMVar_hsa_circ_6805,RMVar_hsa_circ_119423,RMVar_hsa_circ_340235,RMVar_hsa_circ_354059,RMVar_hsa_circ_315235,RMVar_hsa_circ_139882,RMVar_hsa_circ_4093,RMVar_hsa_circ_57943,RMVar_hsa_circ_139880,RMVar_hsa_circ_139881,RMVar_hsa_circ_300897,RMVar_hsa_circ_61902,RMVar_hsa_circ_27780,RMVar_hsa_circ_91491,RMVar_hsa_circ_139889,RMVar_hsa_circ_373930,RMVar_hsa_circ_26004,RMVar_hsa_circ_139891,RMVar_hsa_circ_64892,RMVar_hsa_circ_357811,RMVar_hsa_circ_301018,RMVar_hsa_circ_139892,RMVar_hsa_circ_364188,RMVar_hsa_circ_29261,RMVar_hsa_circ_282823,RMVar_hsa_circ_28085,RMVar_hsa_circ_271569,RMVar_hsa_circ_139893,RMVar_hsa_circ_139894,RMVar_hsa_circ_282848,RMVar_hsa_circ_288757,RMVar_hsa_circ_365120,RMVar_hsa_circ_139898,RMVar_hsa_circ_139899,RMVar_hsa_circ_139897,RMVar_hsa_circ_139902,RMVar_hsa_circ_92575,RMVar_hsa_circ_95509,RMVar_hsa_circ_76377,RMVar_hsa_circ_139903,RMVar_hsa_circ_139906,RMVar_hsa_circ_139901,RMVar_hsa_circ_298586,RMVar_hsa_circ_303149,RMVar_hsa_circ_272614,RMVar_hsa_circ_139905 110420 RMVar_ID_110420 Human_SNP_ID_801134723 m1A Human chr1 + 155320459 155320459 155320459 GAGGCTGAGAAAGTGGCCCGGGTGAAGGCGCTATATGAGGAGCTGGATCTGCCAGCAGTGTTCTT GAGGCTGAGAAAGTGGCCCGGGTGAAGGCGCTGTATGAGGAGCTGGATCTGCCAGCAGTGTTCTT A G FDPS Ensembl:ENSG00000160752 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155320242..155320609 26863196 MeRIP-seq:(Medium) rs760412972 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue Human_RBP_ID_328111,Human_RBP_ID_971588,Human_RBP_ID_1726439,Human_RBP_ID_4082422,Human_RBP_ID_5694332,Human_RBP_ID_8755151,Human_RBP_ID_9356941,Human_RBP_ID_17646164,Human_RBP_ID_17764121,Human_RBP_ID_19198082,Human_RBP_ID_22429717,Human_RBP_ID_22750297,Human_RBP_ID_22847733,Human_RBP_ID_27169124,Human_RBP_ID_27800868 Human_Splice_Rec_138462,Human_Splice_Rec_138494,Human_Splice_Rec_138522,Human_Splice_Rec_138556,Human_Splice_Rec_138600,Human_Splice_Rec_138636,Human_Splice_Rec_138672,Human_Splice_Rec_138678,Human_Splice_Rec_138680 110421 RMVar_ID_110421 Human_SNP_ID_801152433 m1A Human chr1 - 77979004 77979004 77979004 GAACAGGCGGCAGCGGCTCTTATAGTGCAACCATGGCAGACTATTCAACAGTGCCTCCCCCCTCT GAACAGGCGGCAGCGGCTCTTATAGTGCAACCGTGGCAGACTATTCAACAGTGCCTCCCCCCTCT T C FUBP1 Ensembl:ENSG00000162613 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:77978855..77979076;chr1:77978838..77979075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 brain oligodendroglioma,central_nervous_system oligodendroglioma 2 brain Human_RBP_ID_22596,Human_RBP_ID_743897,Human_RBP_ID_2166908,Human_RBP_ID_4074137,Human_RBP_ID_5273098,Human_RBP_ID_5538075,Human_RBP_ID_11115261,Human_RBP_ID_18414990,Human_RBP_ID_26869820 Human_miRNA_ID_2454840,Human_miRNA_ID_2975973 110422 RMVar_ID_110422 Human_SNP_ID_801153093 m1A Human chr1 + 171532852 171532852 171532852 GAACTACAAAAGATGAAAGAACAAGAAAAGGAATGTGAGCTGGAGAAGGAAAGGGAAAAATTAGA GAACTACAAAAGATGAAAGAACAAGAAAAGGAGTGTGAGCTGGAGAAGGAAAGGGAAAAATTAGA A G PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:171532476..171532975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_1530,Human_RBP_ID_1729078,Human_RBP_ID_2103939,Human_RBP_ID_4084845,Human_RBP_ID_5544801,Human_RBP_ID_5712580,Human_RBP_ID_8737846,Human_RBP_ID_9466654,Human_RBP_ID_18555968,Human_RBP_ID_22850043,Human_RBP_ID_23112589,Human_RBP_ID_24541272,Human_RBP_ID_24754214,Human_RBP_ID_26846789 Human_miRNA_ID_1538548,Human_miRNA_ID_1592826,Human_miRNA_ID_2020536,Human_miRNA_ID_2259087,Human_miRNA_ID_2262128,Human_miRNA_ID_2265195 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_97212,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_137543 110423 RMVar_ID_110423 Human_SNP_ID_801167617 m1A Human chr1 + 9269047 9269047 9269047 TGGGGCTCCCTTAGAACTTACTCCACTGATTTAAAAAAAAAAAACTGCCTGGCAGCATCTCAGTG TGGGGCTCCCTTAGAACTTACTCCACTGATTTTAAAAAAAAAAACTGCCTGGCAGCATCTCAGTG A T H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11121355 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue Human_RBP_ID_27401788 Human_miRNA_ID_2278672,Human_miRNA_ID_2458734,Human_miRNA_ID_2638982 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 110424 RMVar_ID_110424 Human_SNP_ID_801170058 m1A Human chr1 + 820993 820993 820993 TGCCTGCAAAGCAGATCCACCCTGTCTACACTACCTGGCTGGCCAGTAGATCCACGCTATCTACA TGCCTGCAAAGCAGATCCACCCTGTCTACACTGCCTGGCTGGCCAGTAGATCCACGCTATCTACA A G FAM87B,lnc-SAMD11-4 RNACentral:URS00008B5E4E,RNACentral:URS00008B984E lincRNA,lincRNA intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:820905..821034 26863196 MeRIP-seq:(Medium) rs1366068885 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110425 RMVar_ID_110425 Human_SNP_ID_801171189 m1A Human chr1 - 154275776 154275776 154275776 ATTCCACATATCCAAGCCCCTGAGGTGGCAAGAGAAGCTAAGCTTATTAATGGTGGGCAATGGGT ATTCCACATATCCAAGCCCCTGAGGTGGCAAGTGAAGCTAAGCTTATTAATGGTGGGCAATGGGT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:154275751..154275825;chr1:154275601..154275800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110426 RMVar_ID_110426 Human_SNP_ID_801175618 m1A Human chr1 + 26282392 26282362 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT GGG______________________________CCGGGACCGGGACAGGGACCAGGACTGAATTT GCCGGGACCGGGACCGGGACTGGGGCCGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 4..33 33 THCA 1 - RMVar_hsa_circ_130641 110427 RMVar_ID_110427 Human_SNP_ID_801188492 m1A Human chr1 - 953259 953258 953259 CAGAGAATGGTGATCGTATGGAGCACTGGGGAAGAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT CAGAGAATGGTGATCGTATGGAGCACTGGGGA_GAGTCTCTGCGGGTGCTGGCTTTCCTGGTCCT CT C NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_223048,Human_RBP_ID_8754549,Human_RBP_ID_18966604 Human_Splice_Rec_1068,Human_Splice_Rec_1069,Human_Splice_Rec_1108,Human_Splice_Rec_1109 Human_miRNA_ID_2255883 RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243 110428 RMVar_ID_110428 Human_SNP_ID_801189598 m1A Human chr1 - 154176154 154176153 154176154 TGCTCAGGAGCGCCTGGCCACTGCCCTGCAAAAGCTGGAAGAAGCTGAAAAAGCTGCTGATGAGA TGCTCAGGAGCGCCTGGCCACTGCCCTGCAAA_GCTGGAAGAAGCTGAAAAAGCTGCTGATGAGA CT C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c chr1:154176151..154176175 31548705,26863196 m1A-IP-seq:(High) - Functional Loss DEL TCGA 33..33 33 LUAD 1 - Human_RBP_ID_222255,Human_RBP_ID_327259,Human_RBP_ID_850431,Human_RBP_ID_1412335,Human_RBP_ID_1726021,Human_RBP_ID_2094960,Human_RBP_ID_5692761,Human_RBP_ID_9356881,Human_RBP_ID_17764088,Human_RBP_ID_26311852,Human_RBP_ID_27800827 Human_Splice_Rec_133470,Human_Splice_Rec_133471,Human_Splice_Rec_133482,Human_Splice_Rec_133483,Human_Splice_Rec_133510,Human_Splice_Rec_133511,Human_Splice_Rec_133524,Human_Splice_Rec_133525,Human_Splice_Rec_133538,Human_Splice_Rec_133539,Human_Splice_Rec_133574,Human_Splice_Rec_133575,Human_Splice_Rec_133602,Human_Splice_Rec_133603,Human_Splice_Rec_133618,Human_Splice_Rec_133619,Human_Splice_Rec_133638,Human_Splice_Rec_133639,Human_Splice_Rec_133652,Human_Splice_Rec_133653,Human_Splice_Rec_133666,Human_Splice_Rec_133667,Human_Splice_Rec_133682,Human_Splice_Rec_133683,Human_Splice_Rec_133700,Human_Splice_Rec_133701,Human_Splice_Rec_133718,Human_Splice_Rec_133719,Human_Splice_Rec_133728,Human_Splice_Rec_133729,Human_Splice_Rec_133739,Human_Splice_Rec_133746,Human_Splice_Rec_133747,Human_Splice_Rec_133754,Human_Splice_Rec_133755 Human_miRNA_ID_1308131,Human_miRNA_ID_2358760 RMVar_hsa_circ_85814,RMVar_hsa_circ_320725,RMVar_hsa_circ_332932,RMVar_hsa_circ_136357 110429 RMVar_ID_110429 Human_SNP_ID_801193344 m1A Human chr1 - 151874650 151874650 151874650 AACTCTCGGGCCAGGCGCTGTGGCTCACACCTATAATCCCAGCACTTTAGGAGGCCGAGGCAGGC AACTCTCGGGCCAGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGC T C THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12045899 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_12194,GWAS_ID_12195,GWAS_ID_12196,GWAS_ID_12197,GWAS_ID_12198 110430 RMVar_ID_110430 Human_SNP_ID_801198435 m1A Human chr1 - 154405645 154405645 154405645 CGGCGCGGCCAGCAGGGCAGCCAGCAGCGCGCAGCCGACGGCCAGCATGCTTCCTCCTCGGCTAC CGGCGCGGCCAGCAGGGCAGCCAGCAGCGCGCGGCCGACGGCCAGCATGCTTCCTCCTCGGCTAC T C IL6R-AS1 Ensembl:ENSG00000228013 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154405599..154405828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110431 RMVar_ID_110431 Human_SNP_ID_801206488 m1A Human chr1 + 160290062 160290062 160290062 AGGTTTTAGGGTACAGAGAGCCAGATCTGAAGAGTAGCTGCAGGGGGAAGGTGCTGTTAGAAGGA AGGTTTTAGGGTACAGAGAGCCAGATCTGAAGTGTAGCTGCAGGGGGAAGGTGCTGTTAGAAGGA A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:160290026..160290100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 110432 RMVar_ID_110432 Human_SNP_ID_801230995 m1A Human chr1 + 15524151 15524151 15524151 CGTCCCAGAGCTGGTCCACCTGCAGCTCTTCCACCAGCCGCAGCCGGCACCGCCGCAGGAGCCGC CGTCCCAGAGCTGGTCCACCTGCAGCTCTTCCCCCAGCCGCAGCCGGCACCGCCGCAGGAGCCGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:15524037..15524448 26863196 MeRIP-seq:(Medium) rs766813971 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 16 head and neck 110433 RMVar_ID_110433 Human_SNP_ID_801231264 m1A Human chr1 - 173866977 173866977 173866977 GATAGCACCTTATGGACAGGTAAGAATTGGGGAAAGTATGGTGGGAAGAATGAAATCTAAGAGGT GATAGCACCTTATGGACAGGTAAGAATTGGGGTAAGTATGGTGGGAAGAATGAAATCTAAGAGGT T A GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:173866976..173867050;chr1:173866976..173867025 26863196,32194978,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2181144,Human_RBP_ID_23345855 Human_Splice_Rec_158950,Human_Splice_Rec_159036,Human_Splice_Rec_159052,Human_Splice_Rec_159074,Human_Splice_Rec_159092,Human_Splice_Rec_159106,Human_Splice_Rec_159128,Human_Splice_Rec_159176,Human_Splice_Rec_159198,Human_Splice_Rec_159210,Human_Splice_Rec_159230,Human_Splice_Rec_159276,Human_Splice_Rec_159290,Human_Splice_Rec_159312,Human_Splice_Rec_159324,Human_Splice_Rec_159332,Human_Splice_Rec_159344 RMVar_hsa_circ_81779,RMVar_hsa_circ_137680,RMVar_hsa_circ_338727,RMVar_hsa_circ_100440,RMVar_hsa_circ_137681,RMVar_hsa_circ_137682,RMVar_hsa_circ_46177,RMVar_hsa_circ_47771,RMVar_hsa_circ_137693,RMVar_hsa_circ_357106,RMVar_hsa_circ_338844,RMVar_hsa_circ_137694,RMVar_hsa_circ_106297,RMVar_hsa_circ_137697,RMVar_hsa_circ_90147,RMVar_hsa_circ_137696,RMVar_hsa_circ_108405,RMVar_hsa_circ_121981,RMVar_hsa_circ_137702,RMVar_hsa_circ_137703 110434 RMVar_ID_110434 Human_SNP_ID_801232809 m1A Human chr1 - 26943007 26943007 26943007 TGCCGTCCTCAATGAGCCACGAGCTCTCCTCCACCTTCACTTCATTGTAGAGCTCCCCATCAATG TGCCGTCCTCAATGAGCCACGAGCTCTCCTCCGCCTTCACTTCATTGTAGAGCTCCCCATCAATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:26942618..26945139;chr1:26942623..26943110;chr1:26942759..26943116 26863196 MeRIP-seq:(Medium) rs1031525845 Functional Loss SNV ICGC 33..33 33 THCA 1 - 110435 RMVar_ID_110435 Human_SNP_ID_801233005 m1A Human chr1 - 904561 904561 904561 CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGAGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG CCACGTTCGGAGGAGGCCACGTTCGGAGGAGGCGGCGGCCGCGTTCGGAGGAGGAGGCGGCCGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:904512..904705 26863196 MeRIP-seq:(Medium) rs1390189362 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110436 RMVar_ID_110436 Human_SNP_ID_801236044 m1A Human chr1 - 944307 944307 944307 CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGAAAATTTGTTCCTTTCCTTTGAAGTCACATTTT CCAGGCTCTGCCTTCACTCCCCCAAGTCTTTGGAAATTTGTTCCTTTCCTTTGAAGTCACATTTT T C NOC2L Ensembl:ENSG00000188976 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2839 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 10 head and neck Human_RBP_ID_5875742,Human_RBP_ID_21999013,Human_RBP_ID_22786394,Human_RBP_ID_27401387 GWAS_ID_7965,GWAS_ID_7966 110437 RMVar_ID_110437 Human_SNP_ID_801236517 m1A Human chr1 + 159855983 159855980 159855983 ACCGCGGGCGCCGCCAGCCCCGGAGCCCCCGCAGCAGCAGCAGACGAGCCCCCAGATGCCTACGG ACCGCGGGCGCCGCCAGCCCCGGAGCCCCC___GCAGCAGCAGACGAGCCCCCAGATGCCTACGG CGCA C AL590560.3 Ensembl:ENSG00000272668 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:159855934..159856066 26863196 MeRIP-seq:(Medium) rs774629452 Functional Loss DEL ICGC 31..33 33 STAD 1 - Human_Splice_Rec_146338 110438 RMVar_ID_110438 Human_SNP_ID_801239541 m1A Human chr1 + 43172174 43172174 43172174 CTACAGGAAGAAACGGGGTATCCCGAGACCCAAGCGGCTAGCAGAGGGCGGCCCTGGCCGCTGCT CTACAGGAAGAAACGGGGTATCCCGAGACCCAGGCGGCTAGCAGAGGGCGGCCCTGGCCGCTGCT A G CFAP57 Ensembl:ENSG00000243710 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43172051..43172273 32194978 MeRIP-seq:(Medium) rs11559314 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,LUSC,large_intestine adenocarcinoma 13 large intestine GWAS_ID_11160,GWAS_ID_11161,GWAS_ID_11162 110439 RMVar_ID_110439 Human_SNP_ID_801240302 m1A Human chr1 + 200620581 200620581 200620581 GCTGAGGAACTGAATGGGGGACTGGAGCTAAGACCACCCGCCCGCAGAGCAGTGGTCGCCTGTAG GCTGAGGAACTGAATGGGGGACTGGAGCTAAGTCCACCCGCCCGCAGAGCAGTGGTCGCCTGTAG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:200620531..200620678 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 110440 RMVar_ID_110440 Human_SNP_ID_801242862 m1A Human chr1 - 17409090 17409090 17409090 AAACTGCCAGAATACAACCCCCGAACCCTCTGATGCTCCCGGAGACTCCTCCGACTCCACACCTC AAACTGCCAGAATACAACCCCCGAACCCTCTGTTGCTCCCGGAGACTCCTCCGACTCCACACCTC T A RCC2 Ensembl:ENSG00000179051 Protein coding stop codon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:17408989..17409126 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_333912,Human_RBP_ID_1416133,Human_RBP_ID_3288077,Human_RBP_ID_4009672,Human_RBP_ID_5718763,Human_RBP_ID_8738502,Human_RBP_ID_10667753,Human_RBP_ID_17338815,Human_RBP_ID_17456191,Human_RBP_ID_17732016,Human_RBP_ID_22426926,Human_RBP_ID_26372251,Human_RBP_ID_27391427 RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589 110441 RMVar_ID_110441 Human_SNP_ID_801257048 m1A Human chr1 + 42683405 42683405 42683405 TGGCTTGTTTTGCTTTGTTTTCTTTTCCAGCAACGAAGGTTTTGGGAACAGTAAAATGGTTCAAT TGGCTTGTTTTGCTTTGTTTTCTTTTCCAGCAGCGAAGGTTTTGGGAACAGTAAAATGGTTCAAT A G YBX1 Ensembl:ENSG00000065978 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:42683401..42683475 26863196 MeRIP-seq:(Medium) rs772779381 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue marginal_zone_lymphoma,spleen marginal_zone_lymphoma 1 spleen,haematopoietic and lymphoid tissue Human_RBP_ID_17325,Human_RBP_ID_741544,Human_RBP_ID_800796,Human_RBP_ID_859388,Human_RBP_ID_1255869,Human_RBP_ID_1748365,Human_RBP_ID_18187698,Human_RBP_ID_24699251,Human_RBP_ID_27594913 Human_Splice_Rec_56414,Human_Splice_Rec_56415,Human_Splice_Rec_56428,Human_Splice_Rec_56429,Human_Splice_Rec_56447 RMVar_hsa_circ_58394,RMVar_hsa_circ_109677,RMVar_hsa_circ_96779,RMVar_hsa_circ_118671,RMVar_hsa_circ_132185,RMVar_hsa_circ_132186,RMVar_hsa_circ_125874,RMVar_hsa_circ_71356,RMVar_hsa_circ_132187,RMVar_hsa_circ_132188 110442 RMVar_ID_110442 Human_SNP_ID_801258563 m1A Human chr1 - 20633849 20633849 20633849 GATGAGGCCCAGCCCTAGCCCGAAGGCCAGAAAGACTGCCCGGCCGCAAGGGCCCGCGCAGCCCC GATGAGGCCCAGCCCTAGCCCGAAGGCCAGAAGGACTGCCCGGCCGCAAGGGCCCGCGCAGCCCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:20633528..20637859 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 110443 RMVar_ID_110443 Human_SNP_ID_801264028 m1A Human chr1 + 26282392 26282392 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT GGGCCGGGACCGGGACCGGGACTGGGGCCGGGGCCGGGACCGGGACAGGGACCAGGACTGAATTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) rs1134580 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma,skin squamous_cell_carcinoma 19 skin,head and neck,large intestine RMVar_hsa_circ_130641 110444 RMVar_ID_110444 Human_SNP_ID_801277444 m1A Human chr1 + 162023759 162023759 162023759 CAGGAGGGCTCAGGTGGCTGGAAGGCGTTCGGACAGACGCCCGCGGTGCGCGCCGGGACGGGCGG CAGGAGGGCTCAGGTGGCTGGAAGGCGTTCGGGCAGACGCCCGCGGTGCGCGCCGGGACGGGCGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:162023714..162023845 26863196 MeRIP-seq:(Medium) rs114746071 Functional Loss SNV ICGC,COSMIC 33..33 33 MALY,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 2 haematopoietic and lymphoid tissue 110445 RMVar_ID_110445 Human_SNP_ID_801288853 m1A Human chr1 + 146228956 146228956 146228956 CCAGCGCAAATGCCTCGACTCCCCGCGCCCCGAGTCCGCCGCTCCTCGGCCGCCGCCTCAGCCGC CCAGCGCAAATGCCTCGACTCCCCGCGCCCCGGGTCCGCCGCTCCTCGGCCGCCGCCTCAGCCGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:146228865..146228955 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_23889 110446 RMVar_ID_110446 Human_SNP_ID_801288974 m1A Human chr1 - 32817248 32817248 32817248 GCCGGGCTGAGCGGGGGAAGCAGGGGTAGCGGAGCCATGGGGGACGCTCCCAGCCCTGAAGAGAA GCCGGGCTGAGCGGGGGAAGCAGGGGTAGCGGGGCCATGGGGGACGCTCCCAGCCCTGAAGAGAA T C YARS1 Ensembl:ENSG00000134684 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32817149..32817400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_20106,Human_RBP_ID_221988,Human_RBP_ID_803161,Human_RBP_ID_859196,Human_RBP_ID_4046337,Human_RBP_ID_5312444,Human_RBP_ID_8754910,Human_RBP_ID_9252893,Human_RBP_ID_9318818,Human_RBP_ID_22427110,Human_RBP_ID_22531943,Human_RBP_ID_22562822,Human_RBP_ID_23389057,Human_RBP_ID_26862877,Human_RBP_ID_27799993 Human_Splice_Rec_44061,Human_Splice_Rec_44105,Human_Splice_Rec_44125 RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 110447 RMVar_ID_110447 Human_SNP_ID_801292416 m1A Human chr1 - 6124552 6124552 6124552 CCCGGGAGGGCCTCTCCAGGCAGCACGTGCTGACCCGCATCGGGGTCATGTCACTAGTTAGGAAG CCCGGGAGGGCCTCTCCAGGCAGCACGTGCTGTCCCGCATCGGGGTCATGTCACTAGTTAGGAAG T A CHD5 Ensembl:ENSG00000116254 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6124547..6126592 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_359279 Human_Splice_Rec_11417,Human_Splice_Rec_11481,Human_Splice_Rec_11521 110448 RMVar_ID_110448 Human_SNP_ID_801308790 m1A Human chr1 + 26282392 26282386 26282392 GGGCCGGGACCGGGACCGGGACTGGGGCCGGGACCGGGACCGGGACAGGGACCAGGACTGAATTT GGGCCGGGACCGGGACCGGGACTGGGG______CCGGGACCGGGACAGGGACCAGGACTGAATTT GCCGGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26282346..26282463 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 28..33 33 STAD 1 - RMVar_hsa_circ_130641 110449 RMVar_ID_110449 Human_SNP_ID_801310766 m1A Human chr1 + 2587281 2587281 2587281 GGCCCTGGGTCTGCAGGAGTTCCTGGACGGCGACTACTTCGCGGGAGGTGCGTCCTGTTCCCCGC GGCCCTGGGTCTGCAGGAGTTCCTGGACGGCGTCTACTTCGCGGGAGGTGCGTCCTGTTCCCCGC A T PRXL2B Ensembl:ENSG00000157870 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:2587088..2587782 32194978 MeRIP-seq:(Medium) rs1224350440 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 7 kidney Human_Splice_Rec_8059,Human_Splice_Rec_8071,Human_Splice_Rec_8083,Human_Splice_Rec_8095,Human_Splice_Rec_8105,Human_Splice_Rec_8117,Human_Splice_Rec_8129,Human_Splice_Rec_8139,Human_Splice_Rec_8149,Human_Splice_Rec_8161,Human_Splice_Rec_8171,Human_Splice_Rec_8177,Human_Splice_Rec_8187,Human_Splice_Rec_8197 110450 RMVar_ID_110450 Human_SNP_ID_801313516 m1A Human chr1 + 204620189 204620189 204620189 CTCTTCCTTGTCCTCTGGGGCTGGGCCTGCTCAGTCATTGCCAGGCCCCATCAGGGGCAGCCCTG CTCTTCCTTGTCCTCTGGGGCTGGGCCTGCTCGGTCATTGCCAGGCCCCATCAGGGGCAGCCCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:204619810..204620209;chr1:204620069..204620232 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus RMVar_hsa_circ_76688,RMVar_hsa_circ_87144,RMVar_hsa_circ_139162,RMVar_hsa_circ_139170 110451 RMVar_ID_110451 Human_SNP_ID_801326613 m1A Human chr1 - 112956602 112956602 112956602 TCCTCAGTCGCTTCCCGCTACTCCGCACGCGCATCTCCCCCACCCGTCAGGGTCAGGCCTCTCGG TCCTCAGTCGCTTCCCGCTACTCCGCACGCGCCTCTCCCCCACCCGTCAGGGTCAGGCCTCTCGG T G SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:112956471..112956709;chr1:112956495..112956712 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110452 RMVar_ID_110452 Human_SNP_ID_801330878 m1A Human chr1 + 154627896 154627896 154627896 CACTTCCTCGGGACACGGCCGGACACCCGGAGACTGCCAGTGCGGCCGCGACCCTCCCCCCACCC CACTTCCTCGGGACACGGCCGGACACCCGGAGGCTGCCAGTGCGGCCGCGACCCTCCCCCCACCC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:154627810..154627939 26863196 MeRIP-seq:(Medium) rs6426859 Functional Loss SNV ICGC 33..33 33 COCA 5 - 110453 RMVar_ID_110453 Human_SNP_ID_801332289 m1A Human chr1 - 26945454 26945454 26945454 AGCCAGGGCTCACCTTGGAATTCTCAGGGTTAATCTTCTTGGTGTTGATCTCAGGGTCACTGGAC AGCCAGGGCTCACCTTGGAATTCTCAGGGTTATTCTTCTTGGTGTTGATCTCAGGGTCACTGGAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26945376..26945475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_10907092 110454 RMVar_ID_110454 Human_SNP_ID_801337176 m1A Human chr1 - 11948069 11948069 11948069 TCACTGTCTCTGCCTCACCCAGGAAACCCCTTACCTGGATCTTGTAGTTGAAGAACTGAGCTGAG TCACTGTCTCTGCCTCACCCAGGAAACCCCTTGCCTGGATCTTGTAGTTGAAGAACTGAGCTGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11948026..11948122 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110455 RMVar_ID_110455 Human_SNP_ID_801352948 m1A Human chr1 + 224011919 224011919 224011919 ATGGACACGAATGGAACAGAATGGAACGGAATAGACTCGAATGGGATGGAATGGAATTGAATGGA ATGGACACGAATGGAACAGAATGGAACGGAATGGACTCGAATGGGATGGAATGGAATTGAATGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224011731..224011973 26863196 MeRIP-seq:(Medium) rs547456594 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_23366444 110456 RMVar_ID_110456 Human_SNP_ID_801408042 m1A Human chr1 - 233666706 233666706 233666706 AGAGGACCGGCCTGCGGGTGACGTGCACGGTGATGCGCTGGACCACAGCCGTCAGGAACAGGAGG AGAGGACCGGCCTGCGGGTGACGTGCACGGTGGTGCGCTGGACCACAGCCGTCAGGAACAGGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:233666601..233666911 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 110457 RMVar_ID_110457 Human_SNP_ID_801425293 m1A Human chr1 - 1909275 1909275 1909275 CGGATCACCCGGCCCCGCCCCGTCACCCGGCCACGCCCCGTCATCCGGCCACGCCCCGTCACTTC CGGATCACCCGGCCCCGCCCCGTCACCCGGCCCCGCCCCGTCATCCGGCCACGCCCCGTCACTTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1909267..1909408 26863196 MeRIP-seq:(Medium) rs562966514 Functional Loss SNV ICGC 33..33 33 MALY 1 - 110458 RMVar_ID_110458 Human_SNP_ID_801452273 m1A Human chr1 + 8878655 8878655 8878655 CTGCAGACACCGAGGTGAACGTAAAGCCGGCGAGATCTCCGTGCTCCGGGTACCCACAGATACTG CTGCAGACACCGAGGTGAACGTAAAGCCGGCGTGATCTCCGTGCTCCGGGTACCCACAGATACTG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:8878651..8878700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110459 RMVar_ID_110459 Human_SNP_ID_801469909 m1A Human chr1 + 53962326 53962326 53962326 AGGACATCAAAACCGTCAAGCACAAGCTCCAGACCCACATAGGCCTTGTTCACTCCAAAGTGCCT AGGACATCAAAACCGTCAAGCACAAGCTCCAGGCCCACATAGGCCTTGTTCACTCCAAAGTGCCT A G LRRC42 Ensembl:ENSG00000116212 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:53962276..53962325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_Splice_Rec_73370,Human_Splice_Rec_73371,Human_Splice_Rec_73384,Human_Splice_Rec_73385,Human_Splice_Rec_73397 Human_miRNA_ID_2296690,Human_miRNA_ID_2791265 RMVar_hsa_circ_80240,RMVar_hsa_circ_133162,RMVar_hsa_circ_32385,RMVar_hsa_circ_299146,RMVar_hsa_circ_349081,RMVar_hsa_circ_122463,RMVar_hsa_circ_133164,RMVar_hsa_circ_133165,RMVar_hsa_circ_97437,RMVar_hsa_circ_133166 110460 RMVar_ID_110460 Human_SNP_ID_801474713 m1A Human chr1 - 244863671 244863671 244863671 GGGCGAGGCAGGGCCAGCAGCAGGCGGGAGGTAAGAAGAAGGCGGAAGGCGGCGGAGGCGGCGGT GGGCGAGGCAGGGCCAGCAGCAGGCGGGAGGTGAGAAGAAGGCGGAAGGCGGCGGAGGCGGCGGT T C HNRNPU Ensembl:ENSG00000153187 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:244863658..244864106 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_745164,Human_RBP_ID_3332352,Human_RBP_ID_4092614,Human_RBP_ID_5160255,Human_RBP_ID_5339042,Human_RBP_ID_22532195,Human_RBP_ID_22860740,Human_RBP_ID_26315664,Human_RBP_ID_27571466,Human_RBP_ID_27799484 Human_Splice_Rec_207311,Human_Splice_Rec_207407,Human_Splice_Rec_207547 110461 RMVar_ID_110461 Human_SNP_ID_801476222 m1A Human chr1 + 110211758 110211758 110211758 CCGATGGCGGCGGTGTGGGTAGCAGCGGCAGCAGCGGCGGCGGGGGCTGCGAGTTCTTCTTCGAC CCGATGGCGGCGGTGTGGGTAGCAGCGGCAGCGGCGGCGGCGGGGGCTGCGAGTTCTTCTTCGAC A G KCNC4 Ensembl:ENSG00000116396 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110211708..110211860 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 110462 RMVar_ID_110462 Human_SNP_ID_801476924 m1A Human chr1 + 167722038 167722038 167722038 GACCGGAGTGGGGAGCGCGGCGTGGAGGTGCCACCCGGCGCGGGTGGCGGAGAGATCAGAAGCCT GACCGGAGTGGGGAGCGCGGCGTGGAGGTGCCCCCCGGCGCGGGTGGCGGAGAGATCAGAAGCCT A C MPZL1 Ensembl:ENSG00000197965 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:167721951..167722250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_224749,Human_RBP_ID_745806,Human_RBP_ID_4006235,Human_RBP_ID_18416011,Human_RBP_ID_18468633,Human_RBP_ID_22428692,Human_RBP_ID_22870991,Human_RBP_ID_23117679,Human_RBP_ID_26312130 110463 RMVar_ID_110463 Human_SNP_ID_801481348 m1A Human chr1 + 154220575 154220575 154220575 GACCCGGCCTGAAAACATGGCGGACAGGCAGGAGAGCTGGGAAAGGAGAACGACGCCTTCCAGCT GACCCGGCCTGAAAACATGGCGGACAGGCAGGGGAGCTGGGAAAGGAGAACGACGCCTTCCAGCT A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:154220526..154220575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_121210,RMVar_hsa_circ_136366 110464 RMVar_ID_110464 Human_SNP_ID_801485727 m1A Human chr1 - 149886413 149886413 149886413 TTCGTCAACGACATCTTCGAGCGCATCGCGGGAGAGGCTTCCCGCCTGGCGCACTACAACAAGCG TTCGTCAACGACATCTTCGAGCGCATCGCGGGCGAGGCTTCCCGCCTGGCGCACTACAACAAGCG T G H2BC21 Ensembl:ENSG00000184678 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:149886363..149886437 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_224664,Human_RBP_ID_325106,Human_RBP_ID_1149338,Human_RBP_ID_1411066,Human_RBP_ID_8955590,Human_RBP_ID_17679064,Human_RBP_ID_17724650,Human_RBP_ID_18187244,Human_RBP_ID_22429637,Human_RBP_ID_26798797 110465 RMVar_ID_110465 Human_SNP_ID_801494154 m1A Human chr1 - 1045741 1045741 1045741 ACAGTCATCCCGCACGGCGCCTTGGGGATCACAGCTGCAGGCTTTGGGGAAAATCGGGGAGGAAC ACAGTCATCCCGCACGGCGCCTTGGGGATCACCGCTGCAGGCTTTGGGGAAAATCGGGGAGGAAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1045730..1045828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 110466 RMVar_ID_110466 Human_SNP_ID_801506177 m1A Human chr1 - 156671328 156671328 156671328 CGCAGTCTGCAGATGTGCAGAGGTGGGAAGATACGGTGGAGAAGGACCAAGAACTGGCTCAGGAA CGCAGTCTGCAGATGTGCAGAGGTGGGAAGATGCGGTGGAGAAGGACCAAGAACTGGCTCAGGAA T C NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:156670647..156671500;chr1:156669796..156671505 26863196 MeRIP-seq:(Medium) rs375001753 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_22871863,Human_RBP_ID_23117574 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 110467 RMVar_ID_110467 Human_SNP_ID_801520016 m1A Human chr1 + 248855920 248855919 248855921 CCTCTTTAGGTGTGCAGGTGACAGGGGAAGGCAGTAGTCTGGGGGCATCAGGCTCACTACTGAAA CCTCTTTAGGTGTGCAGGTGACAGGGGAAGGC__TAGTCTGGGGGCATCAGGCTCACTACTGAAA CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:248855546..248855980 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 STAD 1 - 110468 RMVar_ID_110468 Human_SNP_ID_801546675 m1A Human chr1 - 19304313 19304313 19304313 GGAGCAGCTGGAGCAGAACTTGGCAGCAACAGAGGAAGGGCCCCTGGAGCCGGCTGTCGTGGATG GGAGCAGCTGGAGCAGAACTTGGCAGCAACAGCGGAAGGGCCCCTGGAGCCGGCTGTCGTGGATG T G AKR7A2 Ensembl:ENSG00000053371 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:19304226..19304350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - Human_RBP_ID_23353721,Human_RBP_ID_27554764 Human_Splice_Rec_25208,Human_Splice_Rec_25218,Human_Splice_Rec_25226,Human_Splice_Rec_25234 RMVar_hsa_circ_129821 110469 RMVar_ID_110469 Human_SNP_ID_801555506 m1A Human chr1 - 53257333 53257333 53257333 ACCAGAACCACAGCACAGAGACACCAAGCCTGACAGCTGCAGTCCCAAGCTCAGTTAGTGTCCCC ACCAGAACCACAGCACAGAGACACCAAGCCTGGCAGCTGCAGTCCCAAGCTCAGTTAGTGTCCCC T C LRP8 Ensembl:ENSG00000157193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53257283..53257404 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_Splice_Rec_72177,Human_Splice_Rec_72217,Human_Splice_Rec_72245,Human_Splice_Rec_72273,Human_Splice_Rec_72309,Human_Splice_Rec_72373,Human_Splice_Rec_72407,Human_Splice_Rec_72415,Human_Splice_Rec_72449,Human_Splice_Rec_72481,Human_Splice_Rec_72505,Human_Splice_Rec_72535,Human_Splice_Rec_72575,Human_Splice_Rec_72613,Human_Splice_Rec_72649,Human_Splice_Rec_72679,Human_Splice_Rec_72709,Human_Splice_Rec_72773,Human_Splice_Rec_72799,Human_Splice_Rec_72807,Human_Splice_Rec_72839,Human_Splice_Rec_72875,Human_Splice_Rec_72893,Human_Splice_Rec_72925,Human_Splice_Rec_72939,Human_Splice_Rec_72951 Human_miRNA_ID_203295,Human_miRNA_ID_1488513,Human_miRNA_ID_2011100,Human_miRNA_ID_2757451 RMVar_hsa_circ_10376,RMVar_hsa_circ_330103,RMVar_hsa_circ_377245,RMVar_hsa_circ_317086,RMVar_hsa_circ_133097,RMVar_hsa_circ_3041,RMVar_hsa_circ_360124,RMVar_hsa_circ_371160,RMVar_hsa_circ_12689,RMVar_hsa_circ_133098 110470 RMVar_ID_110470 Human_SNP_ID_801574073 m1A Human chr1 + 145912491 145912491 145912491 CCAGAACCTTTCAGTCGCCGGCTACAAGCAGAAGACTCTTGCTCCATCAGTAGGCGAATCTCATA CCAGAACCTTTCAGTCGCCGGCTACAAGCAGATGACTCTTGCTCCATCAGTAGGCGAATCTCATA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:145912441..145912542 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck RMVar_hsa_circ_135808,RMVar_hsa_circ_76274 110471 RMVar_ID_110471 Human_SNP_ID_801581687 m1A Human chr1 + 17589784 17589784 17589784 TCTTCCAAGGGTTTATATCTCCAGGGTGGGCCAGGGGTGAAGTTGTGGAGAAACTCAGTCTGGTG TCTTCCAAGGGTTTATATCTCCAGGGTGGGCCTGGGGTGAAGTTGTGGAGAAACTCAGTCTGGTG A T ARHGEF10L Ensembl:ENSG00000074964 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:17589780..17589895 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_129604,RMVar_hsa_circ_105645,RMVar_hsa_circ_356764,RMVar_hsa_circ_366518,RMVar_hsa_circ_369308,RMVar_hsa_circ_374066,RMVar_hsa_circ_368458,RMVar_hsa_circ_364969,RMVar_hsa_circ_365299,RMVar_hsa_circ_364100,RMVar_hsa_circ_307941,RMVar_hsa_circ_341726,RMVar_hsa_circ_352166,RMVar_hsa_circ_308732,RMVar_hsa_circ_285979,RMVar_hsa_circ_114033,RMVar_hsa_circ_60750,RMVar_hsa_circ_97653,RMVar_hsa_circ_99833,RMVar_hsa_circ_103281,RMVar_hsa_circ_87311,RMVar_hsa_circ_92359,RMVar_hsa_circ_87155,RMVar_hsa_circ_129608,RMVar_hsa_circ_129612,RMVar_hsa_circ_129616,RMVar_hsa_circ_129618,RMVar_hsa_circ_129617,RMVar_hsa_circ_129614,RMVar_hsa_circ_129615,RMVar_hsa_circ_129613,RMVar_hsa_circ_129610,RMVar_hsa_circ_129611,RMVar_hsa_circ_129609,RMVar_hsa_circ_129606,RMVar_hsa_circ_129607,RMVar_hsa_circ_129605,RMVar_hsa_circ_129600,RMVar_hsa_circ_129602,RMVar_hsa_circ_129603,RMVar_hsa_circ_129601,RMVar_hsa_circ_41013,RMVar_hsa_circ_364239,RMVar_hsa_circ_65696 110472 RMVar_ID_110472 Human_SNP_ID_801582185 m1A Human chr1 - 30995174 30995174 30995174 AGACAGTGATGAAAACGACAAAGGTGAAAAGAAGAACAAGGGTACGTTTGATGGAGATAAGCTAG AGACAGTGATGAAAACGACAAAGGTGAAAAGAGGAACAAGGGTACGTTTGATGGAGATAAGCTAG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:30995076..30995267 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 7 ovary Human_RBP_ID_351833,Human_RBP_ID_852474,Human_RBP_ID_1745142,Human_RBP_ID_3935642,Human_RBP_ID_8754878,Human_RBP_ID_9443797,Human_RBP_ID_10928282,Human_RBP_ID_17646324,Human_RBP_ID_18571716,Human_RBP_ID_22784206,Human_RBP_ID_23386766 Human_Splice_Rec_39958,Human_Splice_Rec_40000,Human_Splice_Rec_40042,Human_Splice_Rec_40082,Human_Splice_Rec_40156,Human_Splice_Rec_40198,Human_Splice_Rec_40236,Human_Splice_Rec_40354,Human_Splice_Rec_40368 RMVar_hsa_circ_83915,RMVar_hsa_circ_372758,RMVar_hsa_circ_130987,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_67706,RMVar_hsa_circ_131001,RMVar_hsa_circ_111157,RMVar_hsa_circ_45672,RMVar_hsa_circ_131002,RMVar_hsa_circ_296277,RMVar_hsa_circ_71922,RMVar_hsa_circ_53855,RMVar_hsa_circ_131013,RMVar_hsa_circ_116197,RMVar_hsa_circ_346734,RMVar_hsa_circ_307848,RMVar_hsa_circ_131014,RMVar_hsa_circ_46483,RMVar_hsa_circ_131019,RMVar_hsa_circ_273051,RMVar_hsa_circ_303728,RMVar_hsa_circ_82449,RMVar_hsa_circ_118532,RMVar_hsa_circ_131026,RMVar_hsa_circ_60205,RMVar_hsa_circ_47681,RMVar_hsa_circ_131027,RMVar_hsa_circ_131024,RMVar_hsa_circ_131025,RMVar_hsa_circ_354236,RMVar_hsa_circ_131030,RMVar_hsa_circ_116734,RMVar_hsa_circ_131029,RMVar_hsa_circ_275323,RMVar_hsa_circ_355888,RMVar_hsa_circ_379111,RMVar_hsa_circ_281339,RMVar_hsa_circ_274609,RMVar_hsa_circ_131032,RMVar_hsa_circ_131034,RMVar_hsa_circ_131035,RMVar_hsa_circ_131033,RMVar_hsa_circ_131031,RMVar_hsa_circ_64658,RMVar_hsa_circ_64820 110473 RMVar_ID_110473 Human_SNP_ID_801619176 m1A Human chr1 - 153962650 153962650 153962650 TGGCGCCCCGAGGCGGTAGCTTCAGAGCCTCCAGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGC TGGCGCCCCGAGGCGGTAGCTTCAGAGCCTCCGGTGCCTGTGGGGCTGGAGGTGAAGTTGGGGGC T C SLC39A1,AL358472.7 Ensembl:ENSG00000143570,Ensembl:ENSG00000285779 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153962601..153962675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_224147,Human_RBP_ID_745092,Human_RBP_ID_1344847,Human_RBP_ID_4073035,Human_RBP_ID_9319159,Human_RBP_ID_22428590,Human_RBP_ID_22560264 Human_Splice_Rec_132936,Human_Splice_Rec_132942,Human_Splice_Rec_132948,Human_Splice_Rec_132958,Human_Splice_Rec_132964,Human_Splice_Rec_132972,Human_Splice_Rec_132978,Human_Splice_Rec_132986,Human_Splice_Rec_132992,Human_Splice_Rec_132998,Human_Splice_Rec_133006 110474 RMVar_ID_110474 Human_SNP_ID_801647447 m1A Human chr1 - 248855446 248855444 248855446 CTTTCCATTCTTCTCCTCAGGAAAGCTGCCAAAAGAGAGCTGATGCCTTGTGACTTCCCTGGCTG CTTTCCATTCTTCTCCTCAGGAAAGCTGCCAA__GAGAGCTGATGCCTTGTGACTTCCCTGGCTG CTT C ZNF692 Ensembl:ENSG00000171163 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:248855389..248855638 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 STAD 1 - Human_RBP_ID_5332415,Human_RBP_ID_18969804,Human_RBP_ID_24747190 Human_Splice_Rec_209362,Human_Splice_Rec_209363,Human_Splice_Rec_209382,Human_Splice_Rec_209383,Human_Splice_Rec_209402,Human_Splice_Rec_209403,Human_Splice_Rec_209414,Human_Splice_Rec_209415,Human_Splice_Rec_209422,Human_Splice_Rec_209423,Human_Splice_Rec_209436,Human_Splice_Rec_209437,Human_Splice_Rec_209443,Human_Splice_Rec_209464,Human_Splice_Rec_209465,Human_Splice_Rec_209486,Human_Splice_Rec_209487,Human_Splice_Rec_209502,Human_Splice_Rec_209503,Human_Splice_Rec_209514,Human_Splice_Rec_209515,Human_Splice_Rec_209530 RMVar_hsa_circ_39679,RMVar_hsa_circ_30455 110475 RMVar_ID_110475 Human_SNP_ID_801650271 m1A Human chr1 + 154157575 154157575 154157575 GATCAGCCCTCAGTTAAAGGTCAGCTTCCCGCAGGCTGGCCTCAGGCGGAGTCTGGGTCAGAGGG GATCAGCCCTCAGTTAAAGGTCAGCTTCCCGCGGGCTGGCCTCAGGCGGAGTCTGGGTCAGAGGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:154157426..154157725;chr1:154157526..154157600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 110476 RMVar_ID_110476 Human_SNP_ID_801650819 m1A Human chr1 - 183546151 183546151 183546151 TCTGAGGGATTATGGTTATATGGCTCCATGGGAAAAGGCTTCATTTTTTTTTCTAGAGGCTGCTG TCTGAGGGATTATGGTTATATGGCTCCATGGGGAAAGGCTTCATTTTTTTTTCTAGAGGCTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:183546021..183546200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 5 head and neck 110477 RMVar_ID_110477 Human_SNP_ID_801656976 m1A Human chr1 - 6349791 6349791 6349791 GGGGGGACCATCCTGAAGATGATCGAGGAGGCAGGCGCCATCATCAGCACCCGGCATTGCAACAG GGGGGGACCATCCTGAAGATGATCGAGGAGGCTGGCGCCATCATCAGCACCCGGCATTGCAACAG T A ACOT7 Ensembl:ENSG00000097021 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6349751..6349924 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 8 lung Human_RBP_ID_360045,Human_RBP_ID_979399,Human_RBP_ID_4062526,Human_RBP_ID_23407155,Human_RBP_ID_26797554 Human_Splice_Rec_11816,Human_Splice_Rec_11817,Human_Splice_Rec_11832,Human_Splice_Rec_11833,Human_Splice_Rec_11848,Human_Splice_Rec_11849,Human_Splice_Rec_11864,Human_Splice_Rec_11865,Human_Splice_Rec_11880,Human_Splice_Rec_11881,Human_Splice_Rec_11898,Human_Splice_Rec_11899,Human_Splice_Rec_11916,Human_Splice_Rec_11917,Human_Splice_Rec_11932,Human_Splice_Rec_11933,Human_Splice_Rec_11948,Human_Splice_Rec_11949 Human_miRNA_ID_2975429,Human_miRNA_ID_2975430,Human_miRNA_ID_2975431 RMVar_hsa_circ_112671,RMVar_hsa_circ_106361,RMVar_hsa_circ_128631,RMVar_hsa_circ_128630,RMVar_hsa_circ_74572,RMVar_hsa_circ_344202,RMVar_hsa_circ_128634,RMVar_hsa_circ_128635,RMVar_hsa_circ_292935,RMVar_hsa_circ_47085,RMVar_hsa_circ_337462 110478 RMVar_ID_110478 Human_SNP_ID_801661169 m1A Human chr1 - 228316799 228316799 228316799 CATTGATGTACCAGGACGCCTCTCCCACGGGCACCGCCTCGCTGAGCGTGCAGGTGAAGCATGCC CATTGATGTACCAGGACGCCTCTCCCACGGGCCCCGCCTCGCTGAGCGTGCAGGTGAAGCATGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228316749..228316950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110479 RMVar_ID_110479 Human_SNP_ID_801662180 m1A Human chr1 - 153645134 153645134 153645134 TGCTCCTTGGTCAATACAGGGCGAGCAAGGGCACCTCTCCCTCGTCCACGGCCTCGGCCTCGGCC TGCTCCTTGGTCAATACAGGGCGAGCAAGGGCGCCTCTCCCTCGTCCACGGCCTCGGCCTCGGCC T C lnc-S100A13-1 RNACentral:URS00008B8491 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:153645051..153645175 26863196 MeRIP-seq:(Medium) rs1455731990 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine 110480 RMVar_ID_110480 Human_SNP_ID_801674961 m1A Human chr1 - 51825312 51825312 51825312 GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGACATCCTATGGGAAAATTTTTTTGGGGTAAGAT GAAATGTTGTTTGGAAGCCTTGCTAGACCTGGCCATCCTATGGGAAAATTTTTTTGGGGTAAGAT T G NRDC Ensembl:ENSG00000078618 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11205896 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,liver hepatocellular_carcinoma 9 liver Human_RBP_ID_1750062,Human_RBP_ID_3316471,Human_RBP_ID_8750111,Human_RBP_ID_9252940,Human_RBP_ID_9270142 Human_Splice_Rec_69824,Human_Splice_Rec_69825,Human_Splice_Rec_69886,Human_Splice_Rec_69887,Human_Splice_Rec_69948,Human_Splice_Rec_69949,Human_Splice_Rec_70006,Human_Splice_Rec_70007,Human_Splice_Rec_70062,Human_Splice_Rec_70063,Human_Splice_Rec_70130,Human_Splice_Rec_70131,Human_Splice_Rec_70150 GWAS_ID_13375,GWAS_ID_13376,GWAS_ID_13377,GWAS_ID_13378,GWAS_ID_13379 RMVar_hsa_circ_3432,RMVar_hsa_circ_34023,RMVar_hsa_circ_103767,RMVar_hsa_circ_132881,RMVar_hsa_circ_78166,RMVar_hsa_circ_132879,RMVar_hsa_circ_132880,RMVar_hsa_circ_308754,RMVar_hsa_circ_12321,RMVar_hsa_circ_11979,RMVar_hsa_circ_132883,RMVar_hsa_circ_132887,RMVar_hsa_circ_344326,RMVar_hsa_circ_303176,RMVar_hsa_circ_55941,RMVar_hsa_circ_132888,RMVar_hsa_circ_294881,RMVar_hsa_circ_74765,RMVar_hsa_circ_343054,RMVar_hsa_circ_356702,RMVar_hsa_circ_53311,RMVar_hsa_circ_132894,RMVar_hsa_circ_364064,RMVar_hsa_circ_347463,RMVar_hsa_circ_276938,RMVar_hsa_circ_11179,RMVar_hsa_circ_66780,RMVar_hsa_circ_132899,RMVar_hsa_circ_360507,RMVar_hsa_circ_62314,RMVar_hsa_circ_280188,RMVar_hsa_circ_340806,RMVar_hsa_circ_303293,RMVar_hsa_circ_132902,RMVar_hsa_circ_41692,RMVar_hsa_circ_132901,RMVar_hsa_circ_291210,RMVar_hsa_circ_355688,RMVar_hsa_circ_62713,RMVar_hsa_circ_5550,RMVar_hsa_circ_132903,RMVar_hsa_circ_132904,RMVar_hsa_circ_48711,RMVar_hsa_circ_60868,RMVar_hsa_circ_274550,RMVar_hsa_circ_343639,RMVar_hsa_circ_359022,RMVar_hsa_circ_362060,RMVar_hsa_circ_294034,RMVar_hsa_circ_132906,RMVar_hsa_circ_132907,RMVar_hsa_circ_98685,RMVar_hsa_circ_132908 110481 RMVar_ID_110481 Human_SNP_ID_801676286 m1A Human chr1 - 37475491 37475491 37475491 AGGCTTCTCTCCACAGGGGCCACTCATAGCTCAGACTCCTGGAAGGCCCCGCGCCACAGCTCCTA AGGCTTCTCTCCACAGGGGCCACTCATAGCTCTGACTCCTGGAAGGCCCCGCGCCACAGCTCCTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:37475472..37475762 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRP 1 - 110482 RMVar_ID_110482 Human_SNP_ID_801676384 m1A Human chr1 - 1787408 1787408 1787408 CAGGTGTCTTGGCTGGGCATGACAACCGCGTCAGCTGCCTGGGCGTGACTGACGATGGCATGGCT CAGGTGTCTTGGCTGGGCATGACAACCGCGTCGGCTGCCTGGGCGTGACTGACGATGGCATGGCT T C GNB1 Ensembl:ENSG00000078369 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1787290..1787477 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,UCEC,large_intestine adenocarcinoma 9 large intestine Human_RBP_ID_333014,Human_RBP_ID_5713497,Human_RBP_ID_8738071,Human_RBP_ID_22426815,Human_RBP_ID_22632702 Human_Splice_Rec_6154,Human_Splice_Rec_6155,Human_Splice_Rec_6172,Human_Splice_Rec_6173,Human_Splice_Rec_6194,Human_Splice_Rec_6195 RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_96576,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_88726,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128387,RMVar_hsa_circ_128397,RMVar_hsa_circ_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_376755,RMVar_hsa_circ_369314,RMVar_hsa_circ_94091,RMVar_hsa_circ_104378,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_128398,RMVar_hsa_circ_128396 110483 RMVar_ID_110483 Human_SNP_ID_801688780 m1A Human chr1 - 150231889 150231889 150231889 AGAGTTAGTCCTTGATAATTGCCTGTGTGTCAATGGGGAAATTGAAGGCCTGAATGATACTTTCA AGAGTTAGTCCTTGATAATTGCCTGTGTGTCAGTGGGGAAATTGAAGGCCTGAATGATACTTTCA T C ANP32E Ensembl:ENSG00000143401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150231838..150231984 26863196 MeRIP-seq:(Medium) rs782794752 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast lobular_carcinoma 8 breast Human_RBP_ID_21092,Human_RBP_ID_325354,Human_RBP_ID_1411217,Human_RBP_ID_1724905,Human_RBP_ID_2092770,Human_RBP_ID_3991462,Human_RBP_ID_5458344,Human_RBP_ID_8940013,Human_RBP_ID_8955699,Human_RBP_ID_9356775,Human_RBP_ID_17204280,Human_RBP_ID_18550857,Human_RBP_ID_23330731,Human_RBP_ID_26311743,Human_RBP_ID_27798478 Human_Splice_Rec_125916,Human_Splice_Rec_125936,Human_Splice_Rec_125948,Human_Splice_Rec_125962,Human_Splice_Rec_125980 Human_miRNA_ID_1180931,Human_miRNA_ID_1965171,Human_miRNA_ID_2360624,Human_miRNA_ID_2782022,Human_miRNA_ID_2784990 RMVar_hsa_circ_66515,RMVar_hsa_circ_349491,RMVar_hsa_circ_276670 110484 RMVar_ID_110484 Human_SNP_ID_801697485 m1A Human chr1 - 89994914 89994914 89994914 AAGGAGCGCTAAAGATTGGCGGGGGTTGTGGGAAAGCAAGCCGAGTGTACGGGAAGGGCCGGCTG AAGGAGCGCTAAAGATTGGCGGGGGTTGTGGGGAAGCAAGCCGAGTGTACGGGAAGGGCCGGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:89994866..89994951 26863196 MeRIP-seq:(Medium) rs1354731249 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110485 RMVar_ID_110485 Human_SNP_ID_801698477 m1A Human chr1 + 45693719 45693719 45693719 TTCCTTATTTCTGAAAGACTTAGTGAAGCCATAGTCACAGTAATAATGGGTATGGGAGTAGCATT TTCCTTATTTCTGAAAGACTTAGTGAAGCCATGGTCACAGTAATAATGGGTATGGGAGTAGCATT A G TMEM69 Ensembl:ENSG00000159596 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45693646..45693796 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_356593 110486 RMVar_ID_110486 Human_SNP_ID_801698932 m1A Human chr1 + 161526241 161526241 161526241 GGAGAGGATGGTTCATGAAGCCGAGCAGTACAAGGCTGAGGATGAGGCCCAGAGGGACAGAGTGG GGAGAGGATGGTTCATGAAGCCGAGCAGTACAGGGCTGAGGATGAGGCCCAGAGGGACAGAGTGG A G AL590385.2,HSPA6 Ensembl:ENSG00000273112,Ensembl:ENSG00000173110 lincRNA,Protein coding intron,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:161526130..161526281 26863196 MeRIP-seq:(Medium) rs570167 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_23302936 RMVar_hsa_circ_113318,RMVar_hsa_circ_137164 110487 RMVar_ID_110487 Human_SNP_ID_801720425 m1A Human chr1 - 16631096 16631096 16631096 TTCCCTCCCTTACCCTCAGGCCGTCCTGTCTGACGCTGAGAGCGGCAGCCTGCGTCCAACAGCGT TTCCCTCCCTTACCCTCAGGCCGTCCTGTCTGTCGCTGAGAGCGGCAGCCTGCGTCCAACAGCGT T A CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16630883..16633135 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_849501,Human_RBP_ID_3935243,Human_RBP_ID_5334811,Human_RBP_ID_17668399,Human_RBP_ID_18409157,Human_RBP_ID_18964752,Human_RBP_ID_19034019,Human_RBP_ID_22562338,Human_RBP_ID_22632927,Human_RBP_ID_23112642,Human_RBP_ID_24747944 Human_Splice_Rec_22690,Human_Splice_Rec_22712,Human_Splice_Rec_22742,Human_Splice_Rec_22760 RMVar_hsa_circ_11074,RMVar_hsa_circ_33194,RMVar_hsa_circ_18591,RMVar_hsa_circ_34197,RMVar_hsa_circ_45680,RMVar_hsa_circ_29922 110488 RMVar_ID_110488 Human_SNP_ID_801723088 m1A Human chr1 + 44113546 44113546 44113546 ACCTAGGCCAGCCTGGGTATCAGGGAAGGCATAAGACAGGTAGGAGTTGGGTGGGGGAAGCATTA ACCTAGGCCAGCCTGGGTATCAGGGAAGGCATGAGACAGGTAGGAGTTGGGTGGGGGAAGCATTA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44113498..44113596 26863196 MeRIP-seq:(Medium) rs1232866430 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110489 RMVar_ID_110489 Human_SNP_ID_801746282 m1A Human chr1 - 156742955 156742955 156742955 TGGGGGCAGCACAGGAGGGCGGCCTCCTTCTGAGCTCCTGTCCCCTGCTACACCTATTATCCCAG TGGGGGCAGCACAGGAGGGCGGCCTCCTTCTGTGCTCCTGTCCCCTGCTACACCTATTATCCCAG T A HDGF Ensembl:ENSG00000143321 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156742904..156743475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_222165,Human_RBP_ID_329048,Human_RBP_ID_743152,Human_RBP_ID_1150025,Human_RBP_ID_8168420,Human_RBP_ID_9352397,Human_RBP_ID_10609743,Human_RBP_ID_17727586,Human_RBP_ID_18553625,Human_RBP_ID_22780739,Human_RBP_ID_26386565,Human_RBP_ID_26844118,Human_RBP_ID_27389566,Human_RBP_ID_27554504 Human_miRNA_ID_721969,Human_miRNA_ID_831834,Human_miRNA_ID_2290928,Human_miRNA_ID_2356274,Human_miRNA_ID_3058718 RMVar_hsa_circ_82179,RMVar_hsa_circ_117608,RMVar_hsa_circ_119732,RMVar_hsa_circ_108690,RMVar_hsa_circ_115770,RMVar_hsa_circ_99168,RMVar_hsa_circ_136900,RMVar_hsa_circ_136902,RMVar_hsa_circ_136904,RMVar_hsa_circ_136905,RMVar_hsa_circ_136903,RMVar_hsa_circ_136901 110490 RMVar_ID_110490 Human_SNP_ID_801758695 m1A Human chr1 - 112647207 112647207 112647207 ATGAGTGATGAATTTAGCAGCTATGCGTACCTAAAGAGAAACAAAATTTACACTTAGGAGAATTA ATGAGTGATGAATTTAGCAGCTATGCGTACCTGAAGAGAAACAAAATTTACACTTAGGAGAATTA T C lnc-ST7L-5,lnc-ST7L-5:2,RF00017-071,lnc-ST7L-5:3 RNACentral:URS00008BCA23,RNACentral:URS00008B26DB,RNACentral:URS00009310A4,RNACentral:URS00008B64AA lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:112647201..112647225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 110491 RMVar_ID_110491 Human_SNP_ID_801769050 m1A Human chr1 + 43598648 43598648 43598648 CTGGGGGAGTGGGGTGCTGAGGCAGGACCCTCAAGTTTGCTGTGCCCACCTGAGCTAGGGTTGAT CTGGGGGAGTGGGGTGCTGAGGCAGGACCCTCGAGTTTGCTGTGCCCACCTGAGCTAGGGTTGAT A G PTPRF Ensembl:ENSG00000142949 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17849103 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_22535198,Human_RBP_ID_22864424 GWAS_ID_11163,GWAS_ID_11164,GWAS_ID_11165,GWAS_ID_11166 RMVar_hsa_circ_107142,RMVar_hsa_circ_266236,RMVar_hsa_circ_91125,RMVar_hsa_circ_132295,RMVar_hsa_circ_132292,RMVar_hsa_circ_132293,RMVar_hsa_circ_80635,RMVar_hsa_circ_267194,RMVar_hsa_circ_79921,RMVar_hsa_circ_97671,RMVar_hsa_circ_132299,RMVar_hsa_circ_127388,RMVar_hsa_circ_132304,RMVar_hsa_circ_132305,RMVar_hsa_circ_115377,RMVar_hsa_circ_84667,RMVar_hsa_circ_81129,RMVar_hsa_circ_132306,RMVar_hsa_circ_132308,RMVar_hsa_circ_21186,RMVar_hsa_circ_66818,RMVar_hsa_circ_132309 110492 RMVar_ID_110492 Human_SNP_ID_801772409 m1A Human chr1 - 159884488 159884486 159884489 GCGATCGCTGCTTGCTGAGCAGCGGGAGCAGGAGAAGGAGCAGATGCTGGAATATATGGAACAGC GCGATCGCTGCTTGCTGAGCAGCGGGAGCAG___AAGGAGCAGATGCTGGAATATATGGAACAGC TCTC T CFAP45 Ensembl:ENSG00000213085 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:159884436..159884547 26863196 MeRIP-seq:(Medium) rs753806120 Functional Loss DEL TCGA 32..34 33 COAD 1 - Human_Splice_Rec_146354,Human_Splice_Rec_146355,Human_Splice_Rec_146376,Human_Splice_Rec_146377,Human_Splice_Rec_146398,Human_Splice_Rec_146399 110493 RMVar_ID_110493 Human_SNP_ID_801776051 m1A Human chr1 + 109235325 109235325 109235325 TGCCCTGCACCGGGATGAGTGGCTCCGGCCGGAGGACCTGCCCATCAAGTATGCTGGCCTGTCTA TGCCCTGCACCGGGATGAGTGGCTCCGGCCGGTGGACCTGCCCATCAAGTATGCTGGCCTGTCTA A T SARS1 Ensembl:ENSG00000031698 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:109231626..109236125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_220994,Human_RBP_ID_320136,Human_RBP_ID_969660,Human_RBP_ID_1407601,Human_RBP_ID_9252955,Human_RBP_ID_10506661,Human_RBP_ID_18965761,Human_RBP_ID_22428487,Human_RBP_ID_23320922,Human_RBP_ID_26309786,Human_RBP_ID_27385375 RMVar_hsa_circ_33424,RMVar_hsa_circ_92435,RMVar_hsa_circ_135152 110494 RMVar_ID_110494 Human_SNP_ID_801783053 m1A Human chr1 + 72282415 72282415 72282415 CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCAGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCTGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:72282367..72282724 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung 110495 RMVar_ID_110495 Human_SNP_ID_801783056 m1A Human chr1 + 72282415 72282415 72282415 CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCAGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC CACTCTGTCCAGCCGGGAGGCAGGAGGGTAGCGGGCAGCACAGGCTGAGGAGCACCGCCGCCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:72282367..72282724 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 1 stomach 110496 RMVar_ID_110496 Human_SNP_ID_801810348 m1A Human chr1 + 31577327 31577324 31577327 GGAGCAGGACCTGTGCTGCCGCGGCCGTGCCGACGACTGTGCCCTGCCCTACCTGGGCGCCATCT GGAGCAGGACCTGTGCTGCCGCGGCCGTGC___CGACTGTGCCCTGCCCTACCTGGGCGCCATCT CCGA C TINAGL1,LINC01226 Ensembl:ENSG00000142910,Ensembl:ENSG00000284543 Protein coding,lincRNA CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31577276..31577397 26863196 MeRIP-seq:(Medium) rs1192018462 Functional Loss DEL TCGA 31..33 33 UCEC 1 - Human_RBP_ID_4075365 RMVar_hsa_circ_82606,RMVar_hsa_circ_131087 110497 RMVar_ID_110497 Human_SNP_ID_801821171 m1A Human chr1 + 109627267 109627267 109627267 CCATGCCTGGGGACCTGGGCTTGGGTCTGCGCATGGTGCGGGGTGTGGTGCACGTCTACACCCGC CCATGCCTGGGGACCTGGGCTTGGGTCTGCGCTTGGTGCGGGGTGTGGTGCACGTCTACACCCGC A T AMPD2 Ensembl:ENSG00000116337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109627115..109627266 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_RBP_ID_8754067 Human_Splice_Rec_106218,Human_Splice_Rec_106219,Human_Splice_Rec_106250,Human_Splice_Rec_106251,Human_Splice_Rec_106284,Human_Splice_Rec_106285,Human_Splice_Rec_106320,Human_Splice_Rec_106321,Human_Splice_Rec_106374,Human_Splice_Rec_106375,Human_Splice_Rec_106406,Human_Splice_Rec_106407,Human_Splice_Rec_106438,Human_Splice_Rec_106439,Human_Splice_Rec_106470,Human_Splice_Rec_106471,Human_Splice_Rec_106514,Human_Splice_Rec_106515,Human_Splice_Rec_106548,Human_Splice_Rec_106549,Human_Splice_Rec_106582,Human_Splice_Rec_106583,Human_Splice_Rec_106614,Human_Splice_Rec_106626,Human_Splice_Rec_106627,Human_Splice_Rec_106662,Human_Splice_Rec_106663 110498 RMVar_ID_110498 Human_SNP_ID_801838517 m1A Human chr1 - 228300051 228300051 228300051 TCTGCTATGACCAGGCCACGAATCTGCAGCTCACAACTGGTCCCATCCTGCTTCAGGCTGTACCT TCTGCTATGACCAGGCCACGAATCTGCAGCTCCCAACTGGTCCCATCCTGCTTCAGGCTGTACCT T G AL353593.2 Ensembl:ENSG00000270110 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:228300009..228300160 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 5 oesophagus 110499 RMVar_ID_110499 Human_SNP_ID_801861289 m1A Human chr1 + 77779729 77779729 77779729 TGGCGTGGGCAGGCCAGCTGTACCTGGCCTGGAGCTCCAGGTACAGGGCCAGGGGCGGGGTGGGG TGGCGTGGGCAGGCCAGCTGTACCTGGCCTGGCGCTCCAGGTACAGGGCCAGGGGCGGGGTGGGG A C MIGA1 Ensembl:ENSG00000180488 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:77779680..77780039 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_88575,Human_Splice_Rec_88605,Human_Splice_Rec_88635,Human_Splice_Rec_88663,Human_Splice_Rec_88695,Human_Splice_Rec_88723 110500 RMVar_ID_110500 Human_SNP_ID_801862117 m1A Human chr1 + 6785519 6785517 6785520 GTACGAGGCGCGCGCTCGGGGTCCCGGTCGCGAGGAGGAGGAGGATGTGGCGCGCGGAGGGGAAA GTACGAGGCGCGCGCTCGGGGTCCCGGTCGC___GAGGAGGAGGATGTGGCGCGCGGAGGGGAAA CGAG C CAMTA1 Ensembl:ENSG00000171735 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:6785476..6785638 26863196 MeRIP-seq:(Medium) rs755609750 Functional Loss DEL ICGC 32..34 33 PAAD 2 - Human_RBP_ID_102,Human_RBP_ID_25666,Human_RBP_ID_361162,Human_RBP_ID_4064475,Human_RBP_ID_5311514,Human_RBP_ID_5857363,Human_RBP_ID_8227944,Human_RBP_ID_8939936,Human_RBP_ID_9318545,Human_RBP_ID_18414840,Human_RBP_ID_22870728,Human_RBP_ID_26310137,Human_RBP_ID_26382766,Human_RBP_ID_27835084 Human_Splice_Rec_13279,Human_Splice_Rec_13283,Human_Splice_Rec_13327,Human_Splice_Rec_13333,Human_Splice_Rec_13339,Human_Splice_Rec_13345,Human_Splice_Rec_13351 110501 RMVar_ID_110501 Human_SNP_ID_801863984 m1A Human chr1 - 154602571 154602571 154602571 CACCCATCCATTTCAAGGCTATGAGCACAGACAGCTCAGGTACCAGCAGCCTGGGCCAGGATCTT CACCCATCCATTTCAAGGCTATGAGCACAGACTGCTCAGGTACCAGCAGCCTGGGCCAGGATCTT T A ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:154602504..154608225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_741774,Human_RBP_ID_4074447,Human_RBP_ID_5458541,Human_RBP_ID_9356924,Human_RBP_ID_18187277,Human_RBP_ID_18552363,Human_RBP_ID_19151595,Human_RBP_ID_26842760 Human_Splice_Rec_134872,Human_Splice_Rec_134900,Human_Splice_Rec_134928,Human_Splice_Rec_134980,Human_Splice_Rec_135008,Human_Splice_Rec_135036,Human_Splice_Rec_135064,Human_Splice_Rec_135092,Human_Splice_Rec_135116,Human_Splice_Rec_135214,Human_Splice_Rec_135216,Human_Splice_Rec_135218,Human_Splice_Rec_135220 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_126815,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203,RMVar_hsa_circ_76145,RMVar_hsa_circ_84571,RMVar_hsa_circ_136457,RMVar_hsa_circ_136458,RMVar_hsa_circ_136459 110502 RMVar_ID_110502 Human_SNP_ID_801869410 m1A Human chr1 - 631386 631386 631386 AGATGCAAGCAGGAGTAGGAGAGAGGGGGGTAAGAGTCAGAAGCTTATGTTGTTTATGCGGGGAA AGATGCAAGCAGGAGTAGGAGAGAGGGGGGTAGGAGTCAGAAGCTTATGTTGTTTATGCGGGGAA T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:631326..631538 26863196 MeRIP-seq:(Medium) rs1431226121 Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_4077355 110503 RMVar_ID_110503 Human_SNP_ID_801883223 m1A Human chr1 + 243254527 243254524 243254528 CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCAACCGCCTCACACCCCAAAACCAATCACACAAA CGCGTCCAAAAGGTTGCTCGCCTGACCTCG____CCGCCTCACACCCCAAAACCAATCACACAAA GCCAA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:243254388..243254533 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 SKCA 1 - RMVar_hsa_circ_141135 110504 RMVar_ID_110504 Human_SNP_ID_801891642 m1A Human chr1 + 65254519 65254519 65254519 GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGAGGGCGCGGCGCACCGATGGGCGCCACTGAGAA GTGGCGCTCGGCTCGGGCGACCGCGGCGGGGGGGGGCGCGGCGCACCGATGGGCGCCACTGAGAA A G DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:65254470..65254625;chr1:65254472..65254636 26863196 MeRIP-seq:(Medium) rs905058342 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_744663,Human_RBP_ID_4063090,Human_RBP_ID_5312577,Human_RBP_ID_8755027,Human_RBP_ID_9318988,Human_RBP_ID_22871316 110505 RMVar_ID_110505 Human_SNP_ID_801907867 m1A Human chr1 + 244048928 244048925 244048928 CACCAAGTCCGGCGGCGGCGGCGGCGGCCGGGAGGAGGAGGAGGAGGAGGCGGAGGACGCGGCGG CACCAAGTCCGGCGGCGGCGGCGGCGGCCG___GGAGGAGGAGGAGGAGGCGGAGGACGCGGCGG GGGA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:244048882..244049001 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 PBCA 1 - Human_Splice_Rec_206849 110506 RMVar_ID_110506 Human_SNP_ID_801919972 m1A Human chr1 - 228103178 228103178 228103178 TGGAGGCGTGCGCGGCGGGCAGGACCAGTTCAACTGGGAGGACGTGAAGACTGACAAGCAGCGGG TGGAGGCGTGCGCGGCGGGCAGGACCAGTTCAGCTGGGAGGACGTGAAGACTGACAAGCAGCGGG T C C1orf35 Ensembl:ENSG00000143793 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:228103126..228103308 26863196 MeRIP-seq:(Medium) rs1238161895 Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_1423106,Human_RBP_ID_1739270,Human_RBP_ID_4074807,Human_RBP_ID_5458566,Human_RBP_ID_5773488,Human_RBP_ID_10823384,Human_RBP_ID_18410008,Human_RBP_ID_18415723,Human_RBP_ID_18565423,Human_RBP_ID_22025667,Human_RBP_ID_23122244,Human_RBP_ID_23370522,Human_RBP_ID_26315531 Human_Splice_Rec_194545,Human_Splice_Rec_194553,Human_Splice_Rec_194565,Human_Splice_Rec_194579,Human_Splice_Rec_194613 110507 RMVar_ID_110507 Human_SNP_ID_801925422 m1A Human chr1 + 9603994 9603994 9603994 GAGTTGGGGCGGGTGAGCCAAAGCGGCCCCCCATGGTGTCTACCTGAGGGGCAGGGAACCGCCTG GAGTTGGGGCGGGTGAGCCAAAGCGGCCCCCCCTGGTGTCTACCTGAGGGGCAGGGAACCGCCTG A C TMEM201 Ensembl:ENSG00000188807 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:9603963..9604035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_125132,RMVar_hsa_circ_128809 110508 RMVar_ID_110508 Human_SNP_ID_801928357 m1A Human chr1 + 19254824 19254824 19254824 CAAAACTGCCAAGAAAGGCTTGGAATTGAAACAAAACCTGATAGAAGAGGTAAGAGGTTGTTCTT CAAAACTGCCAAGAAAGGCTTGGAATTGAAACGAAACCTGATAGAAGAGGTAAGAGGTTGTTCTT A G MRTO4 Ensembl:ENSG00000053372 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:19254801..19254850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22636361 Human_Splice_Rec_25128,Human_Splice_Rec_25129,Human_Splice_Rec_25142,Human_Splice_Rec_25143 RMVar_hsa_circ_126069,RMVar_hsa_circ_72121,RMVar_hsa_circ_337407,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814 110509 RMVar_ID_110509 Human_SNP_ID_801930909 m1A Human chr1 - 55215193 55215193 55215193 CAGGGGCCAACCTGGGCGCGGAGGCGGCGCGGAGGGTGCGCCGCGCGGCCCGCCAGGCCCGGGAC CAGGGGCCAACCTGGGCGCGGAGGCGGCGCGGGGGGTGCGCCGCGCGGCCCGCCAGGCCCGGGAC T C USP24 Ensembl:ENSG00000162402 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:55215142..55215325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4060749 RMVar_hsa_circ_97226,RMVar_hsa_circ_133268 110510 RMVar_ID_110510 Human_SNP_ID_801933201 m1A Human chr1 + 54406062 54406062 54406062 CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGCTACCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC CGAGCCTCGCCGCCGCCGCCGCCGCCGCCGCTGCCGCTCCGGCTCTCCCGAGCTGCCCCTCGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:54405975..54406066;chr1:54405989..54406090 26863410 MeRIP-seq:(Medium) rs1435546926 Functional Loss SNV ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP,liver hepatocellular_carcinoma 10 kidney,liver 110511 RMVar_ID_110511 Human_SNP_ID_801953869 m1A Human chr1 - 153922356 153922356 153922356 CACGCCCCGTTTCCCCCGCCATCCCCGCTTTCACTCCCTGCCTCATGCCCGCCATGCTCCCCTCC CACGCCCCGTTTCCCCCGCCATCCCCGCTTTCCCTCCCTGCCTCATGCCCGCCATGCTCCCCTCC T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:153922348..153922519 26863196 MeRIP-seq:(Medium) rs1464129522 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_3330407,Human_RBP_ID_5125292,Human_RBP_ID_17072464,Human_RBP_ID_18928605,Human_RBP_ID_24398840,Human_RBP_ID_26774531 110512 RMVar_ID_110512 Human_SNP_ID_801991737 m1A Human chr1 + 109548668 109548645 109548668 GCAATAGACGGTGCCTCAGCCTGCCGAGCCGCAGTTTCCGTGGTGTGAGTGAGTCCGGGCCCGTG GCAATAGACG_______________________GTTTCCGTGGTGTGAGTGAGTCCGGGCCCGTG GGTGCCTCAGCCTGCCGAGCCGCA G GNAI3 Ensembl:ENSG00000065135 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109548601..109548850 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 11..33 33 THCA 1 - Human_RBP_ID_1407698,Human_RBP_ID_3980988,Human_RBP_ID_5311788,Human_RBP_ID_8755063,Human_RBP_ID_9270249,Human_RBP_ID_9356637,Human_RBP_ID_22025990,Human_RBP_ID_23321287,Human_RBP_ID_27164535 110513 RMVar_ID_110513 Human_SNP_ID_801992665 m1A Human chr1 + 28335065 28335065 28335065 TTTTGGTTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCGCTTTGTTTCCCAGGCTGGAGTGCA TTTTGGTTTTTGTTTTGTTTTGTTTTTGAGACGGAGTCTCGCTTTGTTTCCCAGGCTGGAGTGCA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 110514 RMVar_ID_110514 Human_SNP_ID_801993010 m1A Human chr1 - 200999932 200999932 200999932 CCCCGAGAAGGAAGCCTTCAAAAAGAGGGCAAAACTCCAACAGGAGAACAGCGAGGAGACGGATG CCCCGAGAAGGAAGCCTTCAAAAAGAGGGCAACACTCCAACAGGAGAACAGCGAGGAGACGGATG T G KIF21B Ensembl:ENSG00000116852 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:200999827..200999965 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 6 uterus Human_RBP_ID_26312470 Human_Splice_Rec_171174,Human_Splice_Rec_171175,Human_Splice_Rec_171240,Human_Splice_Rec_171241,Human_Splice_Rec_171306,Human_Splice_Rec_171307,Human_Splice_Rec_171374,Human_Splice_Rec_171375 RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_67853 110515 RMVar_ID_110515 Human_SNP_ID_801993339 m1A Human chr1 - 156562552 156562552 156562552 AAGAGACCTCGAGCAGGAGTGGTTTGGGGGTGACCTCAGGGTAAGCCCCTGCACTGGGAGGTTTG AAGAGACCTCGAGCAGGAGTGGTTTGGGGGTGCCCTCAGGGTAAGCCCCTGCACTGGGAGGTTTG T G IQGAP3 Ensembl:ENSG00000183856 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7548309 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,lung adenocarcinoma 4 lung Human_RBP_ID_850519,Human_RBP_ID_19039495,Human_RBP_ID_22351944 GWAS_ID_12222,GWAS_ID_12223,GWAS_ID_12224,GWAS_ID_12225,GWAS_ID_12226,GWAS_ID_12227,GWAS_ID_12228,GWAS_ID_12229,GWAS_ID_12230,GWAS_ID_12231,GWAS_ID_12232,GWAS_ID_12233,GWAS_ID_12234,GWAS_ID_12235,GWAS_ID_12236,GWAS_ID_12237,GWAS_ID_12238,GWAS_ID_12239,GWAS_ID_12240 RMVar_hsa_circ_5204,RMVar_hsa_circ_98213,RMVar_hsa_circ_136857,RMVar_hsa_circ_105275,RMVar_hsa_circ_136863,RMVar_hsa_circ_80838,RMVar_hsa_circ_136864,RMVar_hsa_circ_92144,RMVar_hsa_circ_128164,RMVar_hsa_circ_136867,RMVar_hsa_circ_38439,RMVar_hsa_circ_126915,RMVar_hsa_circ_136869,RMVar_hsa_circ_111007,RMVar_hsa_circ_136871,RMVar_hsa_circ_136872,RMVar_hsa_circ_120953,RMVar_hsa_circ_19393,RMVar_hsa_circ_96156,RMVar_hsa_circ_136874,RMVar_hsa_circ_136875,RMVar_hsa_circ_370622,RMVar_hsa_circ_136876 110516 RMVar_ID_110516 Human_SNP_ID_801999025 m1A Human chr1 - 19597051 19597051 19597051 CACCGGTCCCACTTCCTGCCGAGCTCCGACTCAGACATGTTCCCCACCCGCGCCTCCAGCTTTCC CACCGGTCCCACTTCCTGCCGAGCTCCGACTCGGACATGTTCCCCACCCGCGCCTCCAGCTTTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr1:19596959..19597850;chr1:19596976..19600890;chr1:19596951..19597185;chr1:19597001..19597167 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 110517 RMVar_ID_110517 Human_SNP_ID_802002151 m1A Human chr1 - 3625066 3625066 3625066 TCCACCGAGTCCCGCAGTTGCAGCATTGCCGCACCCCTTACCGACCCCGACCCTGACGCCGACGC TCCACCGAGTCCCGCAGTTGCAGCATTGCCGCCCCCCTTACCGACCCCGACCCTGACGCCGACGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:3625015..3625199 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110518 RMVar_ID_110518 Human_SNP_ID_802005884 m1A Human chr1 - 154170463 154170463 154170463 TCTGACTAATTTCATATTTCCCCCAGGCAGAGACCCGTGCTGAGTTTGCTGAGAGATCGGTAGCC TCTGACTAATTTCATATTTCCCCCAGGCAGAGGCCCGTGCTGAGTTTGCTGAGAGATCGGTAGCC T C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:154170349..154170506;chr1:154170382..154170762 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 22 large intestine Human_RBP_ID_222251,Human_RBP_ID_1064554,Human_RBP_ID_5692734,Human_RBP_ID_9356871,Human_RBP_ID_22634345,Human_RBP_ID_22735160,Human_RBP_ID_23333992,Human_RBP_ID_26311839,Human_RBP_ID_27800819 Human_Splice_Rec_133478,Human_Splice_Rec_133479,Human_Splice_Rec_133492,Human_Splice_Rec_133493,Human_Splice_Rec_133498,Human_Splice_Rec_133499,Human_Splice_Rec_133506,Human_Splice_Rec_133507,Human_Splice_Rec_133520,Human_Splice_Rec_133521,Human_Splice_Rec_133534,Human_Splice_Rec_133535,Human_Splice_Rec_133548,Human_Splice_Rec_133549,Human_Splice_Rec_133560,Human_Splice_Rec_133561,Human_Splice_Rec_133566,Human_Splice_Rec_133567,Human_Splice_Rec_133584,Human_Splice_Rec_133585,Human_Splice_Rec_133598,Human_Splice_Rec_133599,Human_Splice_Rec_133612,Human_Splice_Rec_133613,Human_Splice_Rec_133628,Human_Splice_Rec_133629,Human_Splice_Rec_133634,Human_Splice_Rec_133635,Human_Splice_Rec_133648,Human_Splice_Rec_133649,Human_Splice_Rec_133662,Human_Splice_Rec_133663,Human_Splice_Rec_133676,Human_Splice_Rec_133677,Human_Splice_Rec_133692,Human_Splice_Rec_133693,Human_Splice_Rec_133710,Human_Splice_Rec_133711,Human_Splice_Rec_133716,Human_Splice_Rec_133724 Human_miRNA_ID_2880664 RMVar_hsa_circ_136356,RMVar_hsa_circ_285478,RMVar_hsa_circ_369627,RMVar_hsa_circ_279851,RMVar_hsa_circ_320725 110519 RMVar_ID_110519 Human_SNP_ID_802015590 m1A Human chr1 - 50974089 50974089 50974089 CCACCACCCGGAGGTGGCCTTCTTTGGCAGCCAAGTGCAAGGGCAGGTTCCCTTCATTATCCTCG CCACCACCCGGAGGTGGCCTTCTTTGGCAGCCGAGTGCAAGGGCAGGTTCCCTTCATTATCCTCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:50974038..50974286 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 110520 RMVar_ID_110520 Human_SNP_ID_802032660 m1A Human chr1 - 170074547 170074547 170074547 TCAGGACTGTCATCGCCTCTGGGTGTGAGGGTACTTTGGCCACCGTCCCCGGAAATAACCGCGCC TCAGGACTGTCATCGCCTCTGGGTGTGAGGGTGCTTTGGCCACCGTCCCCGGAAATAACCGCGCC T C KIFAP3 Ensembl:ENSG00000075945 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:170074498..170074598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_26801268 110521 RMVar_ID_110521 Human_SNP_ID_802032670 m1A Human chr1 - 170074547 170074547 170074547 TCAGGACTGTCATCGCCTCTGGGTGTGAGGGTACTTTGGCCACCGTCCCCGGAAATAACCGCGCC TCAGGACTGTCATCGCCTCTGGGTGTGAGGGTTCTTTGGCCACCGTCCCCGGAAATAACCGCGCC T A KIFAP3 Ensembl:ENSG00000075945 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:170074498..170074598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_26801268 110522 RMVar_ID_110522 Human_SNP_ID_802039143 m1A Human chr1 + 154970519 154970519 154970519 GGAGTGGATTGTACTTGGGCTTGGGGGGCAGGAGATCCATAGTTGAGGTGAAAGAGGGGCTGCTG GGAGTGGATTGTACTTGGGCTTGGGGGGCAGGTGATCCATAGTTGAGGTGAAAGAGGGGCTGCTG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:154970501..154970650 26863196 MeRIP-seq:(Medium) rs189263031 Functional Loss SNV ICGC 33..33 33 MALY 1 - 110523 RMVar_ID_110523 Human_SNP_ID_802042552 m1A Human chr1 + 240094533 240094533 240094533 ATACCCAGGGCGGCATAAAGCACAGCCAGAGTATGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT ATACCCAGGGCGGCATAAAGCACAGCCAGAGTGTGTTTGCTCTGGTCAGTGTCAAGCAGTCCAAT A G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs55746338 Functional Loss SNV ICGC 33..33 33 LAML 1 - 110524 RMVar_ID_110524 Human_SNP_ID_802056969 m1A Human chr1 - 235220407 235220407 235220407 AAAGAAATAAAAGTTAAGGAGGAAAATGAAACAGAGATCAAAGAAATAAAGATGGAGGAGGAGAG AAAGAAATAAAAGTTAAGGAGGAAAATGAAACGGAGATCAAAGAAATAAAGATGGAGGAGGAGAG T C ARID4B Ensembl:ENSG00000054267 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:235220357..235220438 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_4034465,Human_RBP_ID_17646758,Human_RBP_ID_24541742,Human_RBP_ID_26312907 RMVar_hsa_circ_4746,RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_109816,RMVar_hsa_circ_59555,RMVar_hsa_circ_20448,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_369816,RMVar_hsa_circ_37336,RMVar_hsa_circ_140687,RMVar_hsa_circ_140686,RMVar_hsa_circ_354232,RMVar_hsa_circ_364215,RMVar_hsa_circ_58971,RMVar_hsa_circ_74498,RMVar_hsa_circ_355731,RMVar_hsa_circ_352984,RMVar_hsa_circ_368977,RMVar_hsa_circ_304182,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_325896,RMVar_hsa_circ_140690,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692,RMVar_hsa_circ_333461,RMVar_hsa_circ_366396,RMVar_hsa_circ_301493,RMVar_hsa_circ_321483,RMVar_hsa_circ_75348,RMVar_hsa_circ_140693,RMVar_hsa_circ_140694,RMVar_hsa_circ_3616 110525 RMVar_ID_110525 Human_SNP_ID_802065500 m1A Human chr1 - 26863727 26863727 26863727 TCTCGTAGTGGAAGACGGAAAAGTTCAGGGCCAGGCCCAGGCGGATGGGGTTGGTGGGCGGCATC TCTCGTAGTGGAAGACGGAAAAGTTCAGGGCCTGGCCCAGGCGGATGGGGTTGGTGGGCGGCATC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26863676..26863862 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 110526 RMVar_ID_110526 Human_SNP_ID_802078067 m1A Human chr1 + 26729748 26729748 26729748 CTCGCAGCAACAGGGACCTCCGTCAGGACCGCAGCAAGGACATGGGTACCCAGGGCAGCCATACG CTCGCAGCAACAGGGACCTCCGTCAGGACCGCGGCAAGGACATGGGTACCCAGGGCAGCCATACG A G ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26729699..26731187 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_5137437,Human_RBP_ID_5802526,Human_RBP_ID_8747499,Human_RBP_ID_10905001,Human_RBP_ID_17222325 Human_Splice_Rec_35038,Human_Splice_Rec_35076,Human_Splice_Rec_35116,Human_Splice_Rec_35154 RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_268846,RMVar_hsa_circ_272963,RMVar_hsa_circ_114027,RMVar_hsa_circ_130681,RMVar_hsa_circ_95019,RMVar_hsa_circ_130682,RMVar_hsa_circ_130680 110527 RMVar_ID_110527 Human_SNP_ID_802086139 m1A Human chr1 - 155140243 155140243 155140243 TCAGGGGAGCATTGCTTCCTTCTCTCGCAGTGACCATGACGAAATTAGCGCAGTGGCTTTGGGGA TCAGGGGAGCATTGCTTCCTTCTCTCGCAGTGTCCATGACGAAATTAGCGCAGTGGCTTTGGGGA T A DPM3 Ensembl:ENSG00000179085 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach Human_RBP_ID_3997299,Human_RBP_ID_5109233,Human_RBP_ID_5136390,Human_RBP_ID_5484494,Human_RBP_ID_10594456,Human_RBP_ID_24447595 Human_Splice_Rec_136832,Human_Splice_Rec_136834 RMVar_hsa_circ_119499,RMVar_hsa_circ_136505 110528 RMVar_ID_110528 Human_SNP_ID_802087720 m1A Human chr1 - 207095869 207095869 207095869 GGAGGGAGGCATCTCACATAACAGGTGCAGGAACGAGAGAGGGAGGAGGCGTTACACACTTTTAA GGAGGGAGGCATCTCACATAACAGGTGCAGGAGCGAGAGAGGGAGGAGGCGTTACACACTTTTAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:207095751..207095940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 110529 RMVar_ID_110529 Human_SNP_ID_802088836 m1A Human chr1 - 226379973 226379973 226379973 CAGAGCCTGTTGAAGTTGTGGCCCCAAGAGGGAAGTCAGGGGCTGCGCTCTCCAAAAAAAGCAAG CAGAGCCTGTTGAAGTTGTGGCCCCAAGAGGGGAGTCAGGGGCTGCGCTCTCCAAAAAAAGCAAG T C PARP1 Ensembl:ENSG00000143799 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226379924..226380097 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus Human_RBP_ID_858403,Human_RBP_ID_3300094,Human_RBP_ID_4090033,Human_RBP_ID_5769674,Human_RBP_ID_8228441,Human_RBP_ID_8744219,Human_RBP_ID_9270686,Human_RBP_ID_9359909,Human_RBP_ID_17450426,Human_RBP_ID_19035977,Human_RBP_ID_26312804,Human_RBP_ID_27835405 Human_Splice_Rec_193273 Human_miRNA_ID_2954871 RMVar_hsa_circ_124780,RMVar_hsa_circ_118459,RMVar_hsa_circ_140107,RMVar_hsa_circ_140108 110530 RMVar_ID_110530 Human_SNP_ID_802095805 m1A Human chr1 - 11054870 11054870 11054870 GCCTCATGTCCCTCCAGGCCCTGAATGATGTGAGCTGAGCCCAGGCGCCACCACTGATGCCACCC GCCTCATGTCCCTCCAGGCCCTGAATGATGTGGGCTGAGCCCAGGCGCCACCACTGATGCCACCC T C SRM Ensembl:ENSG00000116649 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:11054576..11054953 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_320816,Human_RBP_ID_1408141,Human_RBP_ID_3276146,Human_RBP_ID_8280758,Human_RBP_ID_8953795,Human_RBP_ID_10516386,Human_RBP_ID_17647329,Human_RBP_ID_17720893,Human_RBP_ID_18547270,Human_RBP_ID_19033870,Human_RBP_ID_22485440,Human_RBP_ID_23322343,Human_RBP_ID_26797662 Human_Splice_Rec_16814,Human_Splice_Rec_16828 Human_miRNA_ID_2268079,Human_miRNA_ID_2552148 RMVar_hsa_circ_82027,RMVar_hsa_circ_107634,RMVar_hsa_circ_114867,RMVar_hsa_circ_109128,RMVar_hsa_circ_92969,RMVar_hsa_circ_103282,RMVar_hsa_circ_84220,RMVar_hsa_circ_129034,RMVar_hsa_circ_129036,RMVar_hsa_circ_129038,RMVar_hsa_circ_75943,RMVar_hsa_circ_129037,RMVar_hsa_circ_129035,RMVar_hsa_circ_129032,RMVar_hsa_circ_129033,RMVar_hsa_circ_129031 110531 RMVar_ID_110531 Human_SNP_ID_802098969 m1A Human chr1 + 224929742 224929742 224929742 GCGTGGTAGGGCTGTGCTGCGCGGTCCTTCCCATTCACCCTAGTCTGGCGCTCGCCGGCGTGGGC GCGTGGTAGGGCTGTGCTGCGCGGTCCTTCCCGTTCACCCTAGTCTGGCGCTCGCCGGCGTGGGC A G DNAH14 Ensembl:ENSG00000185842 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224929691..224929798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 6 breast Human_RBP_ID_745714,Human_RBP_ID_1253201,Human_RBP_ID_4074776,Human_RBP_ID_5311975,Human_RBP_ID_5433625,Human_RBP_ID_5457079,Human_RBP_ID_5485505,Human_RBP_ID_8743886,Human_RBP_ID_9319375,Human_RBP_ID_9359873,Human_RBP_ID_18415718,Human_RBP_ID_19282913,Human_RBP_ID_26854152 Human_Splice_Rec_191751,Human_Splice_Rec_191867,Human_Splice_Rec_192031,Human_Splice_Rec_192043,Human_Splice_Rec_192063,Human_Splice_Rec_192083 110532 RMVar_ID_110532 Human_SNP_ID_802105149 m1A Human chr1 - 155318209 155318209 155318209 AGAGCTTCAGCAGGCGGTAGATACATGCTTCCAGGAGGTTAGCATCATTGATGGCATCCAAACCC AGAGCTTCAGCAGGCGGTAGATACATGCTTCCGGGAGGTTAGCATCATTGATGGCATCCAAACCC T C RUSC1-AS1 Ensembl:ENSG00000225855 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155318170..155318239 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 110533 RMVar_ID_110533 Human_SNP_ID_802116702 m1A Human chr1 + 39576251 39576250 39576251 CGAAGCTCCAAATTTCAAAAAATCAAAGTAGGAAAAAAATTAAACGGGGAATCCCCTTCCGAAGG CGAAGCTCCAAATTTCAAAAAATCAAAGTAGG_AAAAAATTAAACGGGGAATCCCCTTCCGAAGG GA G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:39576226..39576250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - 110534 RMVar_ID_110534 Human_SNP_ID_802116785 m1A Human chr1 + 206406577 206406577 206406577 CAGCAAGAGACAGAGCAGTTTTATTTCACAGTAAGGGAGTGCTATGGCTTTTAAAGAGCGTCAGC CAGCAAGAGACAGAGCAGTTTTATTTCACAGTGAGGGAGTGCTATGGCTTTTAAAGAGCGTCAGC A G SRGAP2 Ensembl:ENSG00000266028 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2772061 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 9 large intestine,haematopoietic and lymphoid tissue RMVar_hsa_circ_17825,RMVar_hsa_circ_20663,RMVar_hsa_circ_278499,RMVar_hsa_circ_311480,RMVar_hsa_circ_330047,RMVar_hsa_circ_340937,RMVar_hsa_circ_1893,RMVar_hsa_circ_291672,RMVar_hsa_circ_276542,RMVar_hsa_circ_2271,RMVar_hsa_circ_349015,RMVar_hsa_circ_60834,RMVar_hsa_circ_69076 110535 RMVar_ID_110535 Human_SNP_ID_802121122 m1A Human chr1 + 156742833 156742833 156742833 AACTACAACTCCCAAAACTCTTGGGGTCGGCAAAAGGAAAAATGGGTGTTGTCAATCATCAAGGA AACTACAACTCCCAAAACTCTTGGGGTCGGCACAAGGAAAAATGGGTGTTGTCAATCATCAAGGA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:156742825..156742951;chr1:156742101..156742900 26863196 MeRIP-seq:(Medium) rs925345802 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 110536 RMVar_ID_110536 Human_SNP_ID_802132808 m1A Human chr1 - 156250450 156250450 156250450 CACGCACACAGGAGGGAGGCCTAGCTGCTCAGAGGCTGCAGGGAGGGCCCAGGAGCCGGCTGGGA CACGCACACAGGAGGGAGGCCTAGCTGCTCAGGGGCTGCAGGGAGGGCCCAGGAGCCGGCTGGGA T C SMG5 Ensembl:ENSG00000198952 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156250426..156250450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_259039,Human_RBP_ID_744472,Human_RBP_ID_3999217,Human_RBP_ID_5109259,Human_RBP_ID_22016403 RMVar_hsa_circ_90375,RMVar_hsa_circ_97584,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,RMVar_hsa_circ_136786,RMVar_hsa_circ_136788,RMVar_hsa_circ_136790,RMVar_hsa_circ_81768,RMVar_hsa_circ_136789,RMVar_hsa_circ_136787 110537 RMVar_ID_110537 Human_SNP_ID_802139293 m1A Human chr1 - 202950882 202950882 202950882 AGGAGTCATCCCCTTGTTCAGTTTCTCTCCTTAGAACTCTGTCATTTTCTCTTTTTTAAGAGCTC AGGAGTCATCCCCTTGTTCAGTTTCTCTCCTTGGAACTCTGTCATTTTCTCTTTTTTAAGAGCTC T C ADIPOR1 Ensembl:ENSG00000159346 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:202950880..202950975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5334062 RMVar_hsa_circ_44820,RMVar_hsa_circ_268295,RMVar_hsa_circ_56413,RMVar_hsa_circ_57249,RMVar_hsa_circ_347464 110538 RMVar_ID_110538 Human_SNP_ID_802141011 m1A Human chr1 - 167220960 167220960 167220960 TGAATATGAATATGTAAAATGCTGTAATGATTACCTGCTGCTGCTGCCGCCGCGGCTGAACTCTC TGAATATGAATATGTAAAATGCTGTAATGATTGCCTGCTGCTGCTGCCGCCGCGGCTGAACTCTC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:167220914..167221051;chr1:167220935..167221027 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110539 RMVar_ID_110539 Human_SNP_ID_802155754 m1A Human chr1 + 21847840 21847840 21847840 ACTCGATCCTGATCGGTGGGGAGACGCTGGGCACTGGGGACAGACGGGTGTGGACCACGCAGCCA ACTCGATCCTGATCGGTGGGGAGACGCTGGGCGCTGGGGACAGACGGGTGTGGACCACGCAGCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21847801..21847850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110540 RMVar_ID_110540 Human_SNP_ID_802164294 m1A Human chr1 + 154974774 154974774 154974774 GATCATGTCGCACAAACAAATTTACTATTCGGACAAATACGACGACGAGGAGTTTGAGTATCGGT GATCATGTCGCACAAACAAATTTACTATTCGGGCAAATACGACGACGAGGAGTTTGAGTATCGGT A G CKS1B Ensembl:ENSG00000173207 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:154974651..154974825;chr1:154974679..154974802 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_RBP_ID_1726341,Human_RBP_ID_4074453 Human_Splice_Rec_135555,Human_Splice_Rec_135559 RMVar_hsa_circ_98035,RMVar_hsa_circ_136483 110541 RMVar_ID_110541 Human_SNP_ID_802180775 m1A Human chr1 - 212697022 212697021 212697022 TGATGACAGGAAGGTCCGAAGGAGAGAAAAAAACCGAGTTGCTGCTCAGAGAAGTCGGAAGAAGC TGATGACAGGAAGGTCCGAAGGAGAGAAAAAA_CCGAGTTGCTGCTCAGAGAAGTCGGAAGAAGC GT G BATF3 Ensembl:ENSG00000123685 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212686741..212697111 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 COAD,STAD 4 - Human_Splice_Rec_186114,Human_Splice_Rec_186115,Human_Splice_Rec_186119 110542 RMVar_ID_110542 Human_SNP_ID_802181694 m1A Human chr1 - 21889982 21889982 21889982 CCCCAGGGATTCCAGTTCCGACGCCTGGGCACAGGTGAGCCTATCCTGGTGTCTGGGATCGCCTC CCCCAGGGATTCCAGTTCCGACGCCTGGGCACTGGTGAGCCTATCCTGGTGTCTGGGATCGCCTC T A HSPG2 Ensembl:ENSG00000142798 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:21889976..21890000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19034212 Human_Splice_Rec_28611,Human_Splice_Rec_28885,Human_Splice_Rec_28895 RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_119604,RMVar_hsa_circ_130231,RMVar_hsa_circ_87462,RMVar_hsa_circ_130261,RMVar_hsa_circ_102017,RMVar_hsa_circ_130315,RMVar_hsa_circ_104207,RMVar_hsa_circ_89670,RMVar_hsa_circ_130321,RMVar_hsa_circ_130324,RMVar_hsa_circ_130326,RMVar_hsa_circ_95647,RMVar_hsa_circ_126790,RMVar_hsa_circ_130332,RMVar_hsa_circ_130338,RMVar_hsa_circ_121542,RMVar_hsa_circ_104762,RMVar_hsa_circ_130339,RMVar_hsa_circ_116722,RMVar_hsa_circ_118308,RMVar_hsa_circ_130343,RMVar_hsa_circ_130344,RMVar_hsa_circ_130348,RMVar_hsa_circ_98883,RMVar_hsa_circ_118968,RMVar_hsa_circ_293281,RMVar_hsa_circ_130349,RMVar_hsa_circ_130350 110543 RMVar_ID_110543 Human_SNP_ID_802183137 m1A Human chr1 + 230279626 230279626 230279626 CTTCGGCAAGGCACGGACGACTGTGCAGACACAGCAGCGGCAAGAAGCGAGAACTGCCCTCCCCC CTTCGGCAAGGCACGGACGACTGTGCAGACACGGCAGCGGCAAGAAGCGAGAACTGCCCTCCCCC A G GALNT2 Ensembl:ENSG00000143641 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:230279576..230279876 32194978 MeRIP-seq:(Medium) rs146911682 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_17223594,Human_RBP_ID_17456595,Human_RBP_ID_24450891,Human_RBP_ID_27177726 110544 RMVar_ID_110544 Human_SNP_ID_802188016 m1A Human chr1 + 26281396 26281396 26281396 CTGGCTGCCCCCAGCCAAGCATTGGGGCCGCCATCCTGCCTGGCACTGGCTGATGGGCACCTCTG CTGGCTGCCCCCAGCCAAGCATTGGGGCCGCCTTCCTGCCTGGCACTGGCTGATGGGCACCTCTG A T SH3BGRL3 Ensembl:ENSG00000142669 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26281376..26281400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_350220,Human_RBP_ID_4093089,Human_RBP_ID_5485957,Human_RBP_ID_17338841,Human_RBP_ID_23303356 RMVar_hsa_circ_118324,RMVar_hsa_circ_113817,RMVar_hsa_circ_130638,RMVar_hsa_circ_107966,RMVar_hsa_circ_130639,RMVar_hsa_circ_130640 110545 RMVar_ID_110545 Human_SNP_ID_802190895 m1A Human chr1 + 247310398 247310398 247310398 CTCCATAGAAGCCAGTCTGGGCAGGATCTAGAAGGGACCAATCCTCTTCAGAGAAGCATAAAATC CTCCATAGAAGCCAGTCTGGGCAGGATCTAGACGGGACCAATCCTCTTCAGAGAAGCATAAAATC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:247310348..247310449 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 110546 RMVar_ID_110546 Human_SNP_ID_802195563 m1A Human chr1 + 156743355 156743355 156743355 GAGTAGAAGAGGAGAGCAGGTTGGGGTGGGAAAGGGGTTCCCAGTTTGCAGGCCATGGCCAGTTT GAGTAGAAGAGGAGAGCAGGTTGGGGTGGGAAGGGGGTTCCCAGTTTGCAGGCCATGGCCAGTTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156742891..156743457 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 110547 RMVar_ID_110547 Human_SNP_ID_802205487 m1A Human chr1 + 154183091 154183091 154183091 CCTGCTGCTGCAGAACCTGGATCTTGCGCTTCACCGCCTCGATGGTGGTGATCCCAGCCATGGTG CCTGCTGCTGCAGAACCTGGATCTTGCGCTTCCCCGCCTCGATGGTGGTGATCCCAGCCATGGTG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:154182951..154183175 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 110548 RMVar_ID_110548 Human_SNP_ID_802206378 m1A Human chr1 - 53328039 53328039 53328039 TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCAGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC TGAAATGCAGCCGAGGAGCCGGGGCGGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGCAGCGGC T C LRP8 Ensembl:ENSG00000157193 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr1:53327944..53328074;chr1:53327940..53328091 26863410 MeRIP-seq:(Medium) rs1340241530 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_101831,Human_RBP_ID_9318955,Human_RBP_ID_18415547 RMVar_hsa_circ_268781 110549 RMVar_ID_110549 Human_SNP_ID_802212505 m1A Human chr1 + 154268887 154268887 154268887 AGCTGCTGCCTACCCACCTGCCCCCTTTATGCACATTCTGACCCCCCATCAGCAGCCGCATTCTC AGCTGCTGCCTACCCACCTGCCCCCTTTATGCGCATTCTGACCCCCCATCAGCAGCCGCATTCTC A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154268837..154268917 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_1250355,Human_RBP_ID_1344879,Human_RBP_ID_17224020,Human_RBP_ID_17338449,Human_RBP_ID_22780258 Human_Splice_Rec_134017,Human_Splice_Rec_134113,Human_Splice_Rec_134193,Human_Splice_Rec_134235,Human_Splice_Rec_134251,Human_Splice_Rec_134277 RMVar_hsa_circ_50165,RMVar_hsa_circ_268210,RMVar_hsa_circ_85521,RMVar_hsa_circ_136386,RMVar_hsa_circ_106489,RMVar_hsa_circ_136401,RMVar_hsa_circ_127313,RMVar_hsa_circ_96950,RMVar_hsa_circ_136415,RMVar_hsa_circ_136414,RMVar_hsa_circ_33569,RMVar_hsa_circ_40871 110550 RMVar_ID_110550 Human_SNP_ID_802217693 m1A Human chr1 - 153613002 153613002 153613002 GGGCTGAGCGCAGGGAGCTGCTTGGCAGTGCCAGAGCCCAGGCCCCAGAGCCCTGCTGGAGAGGA GGGCTGAGCGCAGGGAGCTGCTTGGCAGTGCCGGAGCCCAGGCCCCAGAGCCCTGCTGGAGAGGA T C S100A16 Ensembl:ENSG00000188643 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr1:153612913..153613121;chr1:153612925..153613083 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_98954,Human_RBP_ID_4073027 Human_Splice_Rec_131781,Human_Splice_Rec_131791 Human_miRNA_ID_2422970,Human_miRNA_ID_2432623,Human_miRNA_ID_2552373,Human_miRNA_ID_3067803 RMVar_hsa_circ_113428,RMVar_hsa_circ_136216 110551 RMVar_ID_110551 Human_SNP_ID_802225786 m1A Human chr1 + 156216731 156216731 156216731 GGCGCCCGGGGCGGCCGCGACAACCCCACCCCACTGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC GGCGCCCGGGGCGGCCGCGACAACCCCACCCCGCTGGCTCCGTGCCGTGCGTGTCAGGCGTTCTC A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4119260 Functional Loss SNV COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_II,frontal_lobe oligodendroglioma_Grade_III 21 brain Human_RBP_ID_25410,Human_RBP_ID_269107,Human_RBP_ID_1074460,Human_RBP_ID_1149943,Human_RBP_ID_1344993,Human_RBP_ID_1413215,Human_RBP_ID_2096779,Human_RBP_ID_3283026,Human_RBP_ID_4082664,Human_RBP_ID_5155738,Human_RBP_ID_5272919,Human_RBP_ID_8240234,Human_RBP_ID_8287149,Human_RBP_ID_8735691,Human_RBP_ID_10604989,Human_RBP_ID_18553134,Human_RBP_ID_19200408,Human_RBP_ID_22129135,Human_RBP_ID_22780547,Human_RBP_ID_22848117,Human_RBP_ID_23123115,Human_RBP_ID_23144834,Human_RBP_ID_23303865,Human_RBP_ID_26389885,Human_RBP_ID_26578617,Human_RBP_ID_26843688,Human_RBP_ID_27169487 110552 RMVar_ID_110552 Human_SNP_ID_802227546 m1A Human chr1 - 226402168 226402168 226402168 GGGGCAGCATGGGCATTCAGCCCCCACCCTGAAGCTCCCAGGAGGGCCTCGTCTCAGAGAGCAAA GGGGCAGCATGGGCATTCAGCCCCCACCCTGAGGCTCCCAGGAGGGCCTCGTCTCAGAGAGCAAA T C PARP1 Ensembl:ENSG00000143799 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:226402164..226402326 26863196 MeRIP-seq:(Medium) rs768937503 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 4 skin,head and neck Human_RBP_ID_19044505,Human_RBP_ID_22352015 110553 RMVar_ID_110553 Human_SNP_ID_802272647 m1A Human chr1 + 243254527 243254525 243254528 CGCGTCCAAAAGGTTGCTCGCCTGACCTCGCCAACCGCCTCACACCCCAAAACCAATCACACAAA CGCGTCCAAAAGGTTGCTCGCCTGACCTCGC___CCGCCTCACACCCCAAAACCAATCACACAAA CCAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:243254388..243254533 26863196 MeRIP-seq:(Medium) rs200248716 Functional Loss DEL ICGC 32..34 33 CHOL 5 - GWAS_ID_12785,GWAS_ID_12786,GWAS_ID_12787,GWAS_ID_12788,GWAS_ID_12789,GWAS_ID_12790,GWAS_ID_12791,GWAS_ID_12792,GWAS_ID_12793,GWAS_ID_12794,GWAS_ID_12795,GWAS_ID_12796,GWAS_ID_12797,GWAS_ID_12798,GWAS_ID_12799,GWAS_ID_12800,GWAS_ID_12801,GWAS_ID_12802,GWAS_ID_12803,GWAS_ID_12804,GWAS_ID_12805,GWAS_ID_12806,GWAS_ID_12807,GWAS_ID_12808,GWAS_ID_12809,GWAS_ID_12810,GWAS_ID_12811,GWAS_ID_12812,GWAS_ID_12813,GWAS_ID_12814,GWAS_ID_12815,GWAS_ID_12816,GWAS_ID_12817,GWAS_ID_12818,GWAS_ID_12819,GWAS_ID_12820,GWAS_ID_12821,GWAS_ID_12822,GWAS_ID_12823,GWAS_ID_12824,GWAS_ID_12825,GWAS_ID_12826,GWAS_ID_12827,GWAS_ID_12828,GWAS_ID_12829,GWAS_ID_12830,GWAS_ID_12831,GWAS_ID_12832,GWAS_ID_12833,GWAS_ID_12834,GWAS_ID_12835,GWAS_ID_12836,GWAS_ID_12837,GWAS_ID_12838,GWAS_ID_12839,GWAS_ID_12840,GWAS_ID_12841,GWAS_ID_12842,GWAS_ID_12843,GWAS_ID_12844,GWAS_ID_12845,GWAS_ID_12846,GWAS_ID_12847,GWAS_ID_12848,GWAS_ID_12849,GWAS_ID_12850,GWAS_ID_12851,GWAS_ID_12852,GWAS_ID_12853,GWAS_ID_12854,GWAS_ID_12855,GWAS_ID_12856,GWAS_ID_12857,GWAS_ID_12858,GWAS_ID_12859,GWAS_ID_12860,GWAS_ID_12861,GWAS_ID_12862,GWAS_ID_12863,GWAS_ID_12864,GWAS_ID_12865,GWAS_ID_12866,GWAS_ID_12867,GWAS_ID_12868 RMVar_hsa_circ_141135 110554 RMVar_ID_110554 Human_SNP_ID_802279821 m1A Human chr1 + 226870643 226870643 226870643 CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCAGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC CAGCTGCGTAAACTCCGCTGGAGCGCGGCGGCGGAGCAGGTGAGCGGGCGGTGCCGGGGGGTGCC A G PSEN2 Ensembl:ENSG00000143801 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12758915 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_Splice_Rec_193405,Human_Splice_Rec_193413,Human_Splice_Rec_193437 Human_miRNA_ID_2394315,Human_miRNA_ID_2906249,Human_miRNA_ID_3025079 Clinvar_Rec_453,Clinvar_Rec_454,Clinvar_Rec_455,Clinvar_Rec_456 GWAS_ID_10209,GWAS_ID_10210,GWAS_ID_10211,GWAS_ID_10212,GWAS_ID_10213,GWAS_ID_10214,GWAS_ID_10215,GWAS_ID_10216,GWAS_ID_10217,GWAS_ID_10218,GWAS_ID_10219,GWAS_ID_10220,GWAS_ID_10221,GWAS_ID_10222,GWAS_ID_10223,GWAS_ID_10224,GWAS_ID_10225,GWAS_ID_10226,GWAS_ID_10227,GWAS_ID_10228,GWAS_ID_10229,GWAS_ID_10230,GWAS_ID_10231,GWAS_ID_10232,GWAS_ID_10233,GWAS_ID_10234,GWAS_ID_10235,GWAS_ID_10236,GWAS_ID_10237,GWAS_ID_10238,GWAS_ID_10239,GWAS_ID_10240,GWAS_ID_10241,GWAS_ID_10242,GWAS_ID_10243,GWAS_ID_10244,GWAS_ID_10245,GWAS_ID_10246,GWAS_ID_10247,GWAS_ID_10248,GWAS_ID_10249,GWAS_ID_10250,GWAS_ID_10251,GWAS_ID_10252,GWAS_ID_10253,GWAS_ID_10254,GWAS_ID_10255,GWAS_ID_10256,GWAS_ID_10257,GWAS_ID_10258,GWAS_ID_10259,GWAS_ID_10260,GWAS_ID_10261,GWAS_ID_10262,GWAS_ID_10263,GWAS_ID_10264,GWAS_ID_10265,GWAS_ID_10266,GWAS_ID_10267,GWAS_ID_10268,GWAS_ID_10269,GWAS_ID_10270,GWAS_ID_10271,GWAS_ID_10272,GWAS_ID_10273,GWAS_ID_10274,GWAS_ID_10275,GWAS_ID_10276,GWAS_ID_10277,GWAS_ID_10278,GWAS_ID_10279,GWAS_ID_10280,GWAS_ID_10281,GWAS_ID_10282,GWAS_ID_10283,GWAS_ID_10284,GWAS_ID_10285,GWAS_ID_10286,GWAS_ID_10287,GWAS_ID_10288,GWAS_ID_10289 RMVar_hsa_circ_77887,RMVar_hsa_circ_140112 110555 RMVar_ID_110555 Human_SNP_ID_802283409 m1A Human chr1 + 19911973 19911973 19911973 TCTGACCTATGTCTTTGAAGCAGCTGCTTTGTAGAGTCCCTCTCTTTACTGTCCTCGTTAGGACT TCTGACCTATGTCTTTGAAGCAGCTGCTTTGTGGAGTCCCTCTCTTTACTGTCCTCGTTAGGACT A G OTUD3 Ensembl:ENSG00000169914 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17401847 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_337902,Human_RBP_ID_5739855,Human_RBP_ID_10728156 Human_miRNA_ID_1624678,Human_miRNA_ID_1665175,Human_miRNA_ID_2351033,Human_miRNA_ID_2836857,Human_miRNA_ID_2854733,Human_miRNA_ID_2883855,Human_miRNA_ID_3046579 GWAS_ID_7727,GWAS_ID_7728,GWAS_ID_7729,GWAS_ID_7730 RMVar_hsa_circ_378564,RMVar_hsa_circ_129849,RMVar_hsa_circ_266267 110556 RMVar_ID_110556 Human_SNP_ID_802290620 m1A Human chr1 + 45013141 45013141 45013141 TGAGCCCTGTCTTCCCTCTGTATGCAGAGTTTAGGGAAACCCGGGCTGCCCAGGACTTTTTCAGC TGAGCCCTGTCTTCCCTCTGTATGCAGAGTTTGGGGAAACCCGGGCTGCCCAGGACTTTTTCAGC A G UROD Ensembl:ENSG00000126088 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45013126..45013175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_4055560,Human_RBP_ID_5457733,Human_RBP_ID_8312590,Human_RBP_ID_11005028,Human_RBP_ID_18187116,Human_RBP_ID_22427215 Human_Splice_Rec_62662,Human_Splice_Rec_62663,Human_Splice_Rec_62678,Human_Splice_Rec_62679,Human_Splice_Rec_62686,Human_Splice_Rec_62687,Human_Splice_Rec_62704,Human_Splice_Rec_62708,Human_Splice_Rec_62709,Human_Splice_Rec_62724,Human_Splice_Rec_62725,Human_Splice_Rec_62740,Human_Splice_Rec_62741,Human_Splice_Rec_62756,Human_Splice_Rec_62757,Human_Splice_Rec_62762,Human_Splice_Rec_62763,Human_Splice_Rec_62774,Human_Splice_Rec_62775,Human_Splice_Rec_62790,Human_Splice_Rec_62802,Human_Splice_Rec_62803,Human_Splice_Rec_62814,Human_Splice_Rec_62815,Human_Splice_Rec_62832,Human_Splice_Rec_62833,Human_Splice_Rec_62842,Human_Splice_Rec_62852,Human_Splice_Rec_62853,Human_Splice_Rec_62860,Human_Splice_Rec_62866,Human_Splice_Rec_62867,Human_Splice_Rec_62878,Human_Splice_Rec_62879,Human_Splice_Rec_62900,Human_Splice_Rec_62901,Human_Splice_Rec_62910,Human_Splice_Rec_62911,Human_Splice_Rec_62916,Human_Splice_Rec_62922,Human_Splice_Rec_62923 RMVar_hsa_circ_7870 110557 RMVar_ID_110557 Human_SNP_ID_802295725 m1A Human chr1 + 26863181 26863181 26863181 ACAGAGTCCGGCATTGGTCCCAGGCAGCAGTTAGCCCGCCGCCCGCCTGTGTGTCCCCAGAGCCA ACAGAGTCCGGCATTGGTCCCAGGCAGCAGTTGGCCCGCCGCCCGCCTGTGTGTCCCCAGAGCCA A G SFN Ensembl:ENSG00000175793 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:26863126..26864425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 110558 RMVar_ID_110558 Human_SNP_ID_802316140 m1A Human chr1 - 15943516 15943516 15943516 GGCACCAACACCTTCTGCCCGGTCCCCAGGTGAGAAGCCATGCCAGTGTGTGATGTGCGGTAAGG GGCACCAACACCTTCTGCCCGGTCCCCAGGTGTGAAGCCATGCCAGTGTGTGATGTGCGGTAAGG T A ZBTB17 Ensembl:ENSG00000116809 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:15943422..15943701 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_22557898 Human_Splice_Rec_21454,Human_Splice_Rec_21482,Human_Splice_Rec_21512,Human_Splice_Rec_21524,Human_Splice_Rec_21538,Human_Splice_Rec_21540,Human_Splice_Rec_21544 RMVar_hsa_circ_13802,RMVar_hsa_circ_57754,RMVar_hsa_circ_298171 110559 RMVar_ID_110559 Human_SNP_ID_802317588 m1A Human chr1 - 148522660 148522660 148522660 CAGAGGTCAGCACATCTGGAACGCAATGGATAAGCCGCGACCATGAGAAAAGCGCCTTCATGATC CAGAGGTCAGCACATCTGGAACGCAATGGATACGCCGCGACCATGAGAAAAGCGCCTTCATGATC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:148522601..148522675 26863196 MeRIP-seq:(Medium) rs1382998901 Functional Loss SNV ICGC 33..33 33 LICA 1 - 110560 RMVar_ID_110560 Human_SNP_ID_802332606 m1A Human chr1 + 227431021 227431020 227431022 GGCCTTGTCTGTTAATAAATAGTTTATATACCAAAAAAAAAAAAAAATGCAGAGATAGTGTGGGA GGCCTTGTCTGTTAATAAATAGTTTATATACC__AAAAAAAAAAAAATGCAGAGATAGTGTGGGA CAA C LINC01641 Ensembl:ENSG00000234277 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..34 33 LICA 1 - 110561 RMVar_ID_110561 Human_SNP_ID_802338805 m1A Human chr1 + 634031 634031 634031 CTAGCCATGGCCATCCCCTTATGAGCGGGCGCAGTGATTATAGGCTTTCGCTCTAAGATTAAAAA CTAGCCATGGCCATCCCCTTATGAGCGGGCGCTGTGATTATAGGCTTTCGCTCTAAGATTAAAAA A T MTATP6P1 Ensembl:ENSG00000248527 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:633979..634074;chr1:633916..634143;chr1:633911..634144;chr1:633976..634100;chr1:633932..634102;chr1:633976..634075;chr1:633976..634071 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs574899449 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_1155316,Human_RBP_ID_1432895,Human_RBP_ID_1750919,Human_RBP_ID_3317688,Human_RBP_ID_5156170,Human_RBP_ID_5843585,Human_RBP_ID_8240928,Human_RBP_ID_8315276,Human_RBP_ID_8750691,Human_RBP_ID_17182060,Human_RBP_ID_17336539,Human_RBP_ID_17754745,Human_RBP_ID_21911302,Human_RBP_ID_22488530,Human_RBP_ID_24358601 110562 RMVar_ID_110562 Human_SNP_ID_802340344 m1A Human chr1 + 729360 729360 729360 TGGCCTAAAGAGGCCACTGGGTGGCAGGAGCTAGGTGTGTAGAAGCTGCTGAAAGGTTGGGAGCT TGGCCTAAAGAGGCCACTGGGTGGCAGGAGCTGGGTGTGTAGAAGCTGCTGAAAGGTTGGGAGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:729320..729524 26863196 MeRIP-seq:(Medium) rs75192999 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110563 RMVar_ID_110563 Human_SNP_ID_802343134 m1A Human chr1 - 32336123 32336123 32336123 CCCGGCACCCCTCCCCCTCGGGCGCCAGCCCCACCCCTCCGCCGGCCGGGCCGACCCCGCCGTAC CCCGGCACCCCTCCCCCTCGGGCGCCAGCCCCCCCCCTCCGCCGGCCGGGCCGACCCCGCCGTAC T G MARCKSL1 Ensembl:ENSG00000175130 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:32336024..32336229 26863410 MeRIP-seq:(Medium) rs948852732 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_4072678,Human_RBP_ID_5413927,Human_RBP_ID_5434025,Human_RBP_ID_5457536,Human_RBP_ID_5486140,Human_RBP_ID_23388360 Human_miRNA_ID_2152682,Human_miRNA_ID_2800553,Human_miRNA_ID_3008681 RMVar_hsa_circ_96359,RMVar_hsa_circ_131243 110564 RMVar_ID_110564 Human_SNP_ID_802354352 m1A Human chr1 - 939462 939462 939462 GATGAGGGGAGATCATGCCAGGGTGGGTCCTCACCGTGGCTGGGGAGGTGATGAGGGGGATCATG GATGAGGGGAGATCATGCCAGGGTGGGTCCTCGCCGTGGCTGGGGAGGTGATGAGGGGGATCATG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:939451..939475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110565 RMVar_ID_110565 Human_SNP_ID_802356391 m1A Human chr1 - 161154026 161154026 161154026 CGGCGTTAGTCTTCAGCACCGGGATCTCAGACACAACACGTCGCGTGGCTTCATCCGCCATCTTG CGGCGTTAGTCTTCAGCACCGGGATCTCAGACCCAACACGTCGCGTGGCTTCATCCGCCATCTTG T G AL590714.1 Ensembl:ENSG00000224985 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:161153976..161157025;chr1:161153976..161154151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_Splice_Rec_149826 110566 RMVar_ID_110566 Human_SNP_ID_802382527 m1A Human chr1 + 231421908 231421908 231421908 TGTCATTGGCCATGGCGGCGGCGGCGGCGGCGACGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG TGTCATTGGCCATGGCGGCGGCGGCGGCGGCGGCGGCGACTGCGGCGGCCGAGCAGGAGGGGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:231421862..231421961 26863196 MeRIP-seq:(Medium) rs756211725 Functional Loss SNV ICGC 33..33 33 COCA 1 - Clinvar_Rec_458 110567 RMVar_ID_110567 Human_SNP_ID_802394844 m1A Human chr1 + 166851047 166851047 166851047 GAGCTGCCAGAACATCTGAGAGCTGTAAAGTTAAAATTATTTGGACCCAAAGAAGCATAGTCTGA GAGCTGCCAGAACATCTGAGAGCTGTAAAGTTTAAATTATTTGGACCCAAAGAAGCATAGTCTGA A T POGK Ensembl:ENSG00000143157 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3820387 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate Human_RBP_ID_1728333,Human_RBP_ID_5706642,Human_RBP_ID_8737276,Human_RBP_ID_10636475,Human_RBP_ID_17331159,Human_RBP_ID_18218873,Human_RBP_ID_27580682 GWAS_ID_13387,GWAS_ID_13388 RMVar_hsa_circ_137310 110568 RMVar_ID_110568 Human_SNP_ID_802399281 m1A Human chr1 - 1495915 1495915 1495915 ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTACAAAGCCTCACCCTCCCCCTGTGAGCCAGACG ACCCTCACAGTGGCCTGGGCAGGGGCTGGGGTGCAAAGCCTCACCCTCCCCCTGTGAGCCAGACG T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1495908..1496027 26863196 MeRIP-seq:(Medium) rs1030185265 Functional Loss SNV ICGC 33..33 33 LICA 1 - 110569 RMVar_ID_110569 Human_SNP_ID_802418753 m1A Human chr1 + 224183386 224183386 224183386 GCGGGAAGACTTCGAGTGGGTCTACACCGACCAGCCGCACGCCGACCGGCGCCGGGAGATCCTGG GCGGGAAGACTTCGAGTGGGTCTACACCGACCGGCCGCACGCCGACCGGCGCCGGGAGATCCTGG A G DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:224183251..224183425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_224171,Human_RBP_ID_745111,Human_RBP_ID_4076392 Human_Splice_Rec_190981,Human_Splice_Rec_190985 110570 RMVar_ID_110570 Human_SNP_ID_802448721 m1A Human chr1 - 150811479 150811479 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCACACATGCT T C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61817635 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma,liver hepatocellular_carcinoma 11 liver,prostate Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 110571 RMVar_ID_110571 Human_SNP_ID_802462875 m1A Human chr1 + 247000052 247000052 247000052 ATTCCCACTCCTCTGGAGAGAATTCTAGAGCCACATCCCTGAATGCCAATAGTCCCTGAAAAAGA ATTCCCACTCCTCTGGAGAGAATTCTAGAGCCGCATCCCTGAATGCCAATAGTCCCTGAAAAAGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:247000005..247000114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 110572 RMVar_ID_110572 Human_SNP_ID_802464167 m1A Human chr1 - 154627918 154627918 154627918 GAGAAGGCTACGTGGTGGGGGAGGGTGGGGGGAGGGTCGCGGCCGCACTGGCAGTCTCCGGGTGT GAGAAGGCTACGTGGTGGGGGAGGGTGGGGGGGGGGTCGCGGCCGCACTGGCAGTCTCCGGGTGT T C ADAR Ensembl:ENSG00000160710 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154627806..154627975 26863196 MeRIP-seq:(Medium) rs749763161 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_25396,Human_RBP_ID_224364,Human_RBP_ID_745329,Human_RBP_ID_4073055,Human_RBP_ID_5312686,Human_RBP_ID_5519187,Human_RBP_ID_18415071,Human_RBP_ID_26311878,Human_RBP_ID_26767564 Human_Splice_Rec_134927,Human_Splice_Rec_135217 110573 RMVar_ID_110573 Human_SNP_ID_802476082 m1A Human chr1 - 43305345 43305344 43305345 TACCCTCCCCACCAGTTCAAATGCCCCTCTTTACCGTTGCTCTTCCAGATCACGTCTGTCTGCTT TACCCTCCCCACCAGTTCAAATGCCCCTCTTT_CCGTTGCTCTTCCAGATCACGTCTGTCTGCTT GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43305298..43309084 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LMS 2 - 110574 RMVar_ID_110574 Human_SNP_ID_802484120 m1A Human chr1 - 182383486 182383486 182383486 GGAGAAGGTGGGCACTGGATTAGTTAACAGACAACACGTTACTAGCAGTCACTTGATCTCCGTGG GGAGAAGGTGGGCACTGGATTAGTTAACAGACGACACGTTACTAGCAGTCACTTGATCTCCGTGG T C GLUL Ensembl:ENSG00000135821 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7734 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_334970,Human_RBP_ID_4085805,Human_RBP_ID_5725084,Human_RBP_ID_10687413,Human_RBP_ID_17338575,Human_RBP_ID_18220898,Human_RBP_ID_23349950,Human_RBP_ID_26372875 Human_miRNA_ID_2036212,Human_miRNA_ID_2346911 Clinvar_Rec_283,Clinvar_Rec_2456 GWAS_ID_8383,GWAS_ID_8384 RMVar_hsa_circ_123570,RMVar_hsa_circ_138181 110575 RMVar_ID_110575 Human_SNP_ID_802488374 m1A Human chr1 - 35192727 35192727 35192727 GCAGCCGCCGCCACCGCCGCAGGACTCTTCCAAGCCCGTCGTTGCTCAGGGACCCGGCCCCGCTC GCAGCCGCCGCCACCGCCGCAGGACTCTTCCAGGCCCGTCGTTGCTCAGGGACCCGGCCCCGCTC T C SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:35192501..35193150 26863196 MeRIP-seq:(Medium) rs1283378510 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_803361,Human_RBP_ID_1430212,Human_RBP_ID_1746263,Human_RBP_ID_4047457,Human_RBP_ID_5815456,Human_RBP_ID_8240789,Human_RBP_ID_8309427,Human_RBP_ID_10955218,Human_RBP_ID_17218212,Human_RBP_ID_17452653,Human_RBP_ID_17677686,Human_RBP_ID_18573096,Human_RBP_ID_22531946,Human_RBP_ID_26863476,Human_RBP_ID_27398103 Human_miRNA_ID_1972019,Human_miRNA_ID_1974196 RMVar_hsa_circ_131444,RMVar_hsa_circ_106327,RMVar_hsa_circ_131453,RMVar_hsa_circ_126039 110576 RMVar_ID_110576 Human_SNP_ID_802490880 m1A Human chr1 - 147203893 147203893 147203893 ACACCTCCTGTCCTTGAAGAAATGGGACACTGAGACAGTGTTTACCTCTCAGAAGTTGGAGATAC ACACCTCCTGTCCTTGAAGAAATGGGACACTGTGACAGTGTTTACCTCTCAGAAGTTGGAGATAC T A CCT8P1,FMO5 Ensembl:ENSG00000226015,Ensembl:ENSG00000131781 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879998874 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_miRNA_ID_1827667,Human_miRNA_ID_1838291,Human_miRNA_ID_1851327,Human_miRNA_ID_1851459,Human_miRNA_ID_1851591,Human_miRNA_ID_1851723,Human_miRNA_ID_1851855 RMVar_hsa_circ_70581,RMVar_hsa_circ_339476,RMVar_hsa_circ_353641,RMVar_hsa_circ_350838,RMVar_hsa_circ_71401,RMVar_hsa_circ_362994,RMVar_hsa_circ_357139 110577 RMVar_ID_110577 Human_SNP_ID_802508285 m1A Human chr1 - 204104957 204104957 204104957 CAAACCTAGCCCCTTTCTGCCCAAAACAAATCACCAGCCACTTCCTCTTCTAACCAGTCAACAAC CAAACCTAGCCCCTTTCTGCCCAAAACAAATCCCCAGCCACTTCCTCTTCTAACCAGTCAACAAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:204104954..204105105 26863196 MeRIP-seq:(Medium) rs996052701 Functional Loss SNV ICGC 33..33 33 LICA 1 - 110578 RMVar_ID_110578 Human_SNP_ID_802508381 m1A Human chr1 + 219173941 219173941 219173941 TCGGTTCTGCAGCGCTGTATCGTGTCGCCGGCAGGGAGGCATAGCGCCTCTCTGATCTTCCTGCA TCGGTTCTGCAGCGCTGTATCGTGTCGCCGGCGGGGAGGCATAGCGCCTCTCTGATCTTCCTGCA A G LYPLAL1 Ensembl:ENSG00000143353 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:219173892..219174012 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney Human_RBP_ID_224070,Human_RBP_ID_4074753,Human_RBP_ID_9319360,Human_RBP_ID_22427785,Human_RBP_ID_23364230 Human_Splice_Rec_188527,Human_Splice_Rec_188533,Human_Splice_Rec_188541,Human_Splice_Rec_188547,Human_Splice_Rec_188555,Human_Splice_Rec_188563,Human_Splice_Rec_188581 110579 RMVar_ID_110579 Human_SNP_ID_802525875 m1A Human chr1 - 58783294 58783291 58783295 CAAAGCCGGGTAGCGCGCGCGAGTCGACAAGTAAGAGTGCGGGAGGCATCTTAATTAACCCTGCG CAAAGCCGGGTAGCGCGCGCGAGTCGACAAG____AGTGCGGGAGGCATCTTAATTAACCCTGCG TCTTA T JUN Ensembl:ENSG00000177606 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:58783246..58783500 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..35 33 BRCA 1 - Human_RBP_ID_1433089,Human_RBP_ID_4061203,Human_RBP_ID_5457872,Human_RBP_ID_18578475,Human_RBP_ID_22023436,Human_RBP_ID_22707997,Human_RBP_ID_26867459,Human_RBP_ID_27798131 RMVar_hsa_circ_133352,RMVar_hsa_circ_377802 110580 RMVar_ID_110580 Human_SNP_ID_802543872 m1A Human chr1 - 36177831 36177829 36177831 AAGGGAAAAGGGAAGGGTTAGGAGACACACACACCCACACGCTGAGAACTTGTTCCTTCCTCTGG AAGGGAAAAGGGAAGGGTTAGGAGACACACAC__CCACACGCTGAGAACTTGTTCCTTCCTCTGG GGT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36177829..36178225 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 CHOL 1 - 110581 RMVar_ID_110581 Human_SNP_ID_802547286 m1A Human chr1 - 154602152 154602152 154602152 GGAAGGCCACCACAGCACATGATCTGTCTGGGAAACTTGGGACTCCGAAGAAAGAAATCAATCGA GGAAGGCCACCACAGCACATGATCTGTCTGGGTAACTTGGGACTCCGAAGAAAGAAATCAATCGA T A ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154602102..154602203 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_22113,Human_RBP_ID_327619,Human_RBP_ID_971518,Human_RBP_ID_1412618,Human_RBP_ID_1726309,Human_RBP_ID_3282249,Human_RBP_ID_4076000,Human_RBP_ID_8286270,Human_RBP_ID_8735406,Human_RBP_ID_8956414,Human_RBP_ID_9356922,Human_RBP_ID_10593215,Human_RBP_ID_17764108,Human_RBP_ID_18552357,Human_RBP_ID_22485998,Human_RBP_ID_27388723 Human_Splice_Rec_135194,Human_Splice_Rec_135206 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203 110582 RMVar_ID_110582 Human_SNP_ID_802556895 m1A Human chr1 - 150839656 150839634 150839657 CACCTGGATGGGGCTTCTCTTTCTTTCCATGCAGGGAAAATCACAGTGAAATTGAACGGCGGCGA CACCTGGATGGGGCTTCTCTTTCTTTCCATG_______________________AACGGCGGCGA TCAATTTCACTGTGATTTTCCCTG T ARNT Ensembl:ENSG00000143437 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150839615..150839703 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..54 33 OV 1 - Human_RBP_ID_97588,Human_RBP_ID_22634270,Human_RBP_ID_24585419 RMVar_hsa_circ_19964,RMVar_hsa_circ_75265,RMVar_hsa_circ_92823,RMVar_hsa_circ_135948,RMVar_hsa_circ_22904,RMVar_hsa_circ_4816,RMVar_hsa_circ_47701,RMVar_hsa_circ_57485,RMVar_hsa_circ_344680,RMVar_hsa_circ_52711,RMVar_hsa_circ_32058,RMVar_hsa_circ_54627,RMVar_hsa_circ_72829,RMVar_hsa_circ_85968,RMVar_hsa_circ_135954 110583 RMVar_ID_110583 Human_SNP_ID_802562536 m1A Human chr1 + 23692715 23692715 23692715 GGAGAGTGGAGACAGACTGACGCGAGCAGCCAAGGTGTTGGAGCAGCTCACAGGGCAGACCCCTG GGAGAGTGGAGACAGACTGACGCGAGCAGCCACGGTGTTGGAGCAGCTCACAGGGCAGACCCCTG A C RPL11 Ensembl:ENSG00000142676 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23692666..23692811 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_20641,Human_RBP_ID_347778,Human_RBP_ID_742982,Human_RBP_ID_802166,Human_RBP_ID_976497,Human_RBP_ID_1425671,Human_RBP_ID_1742036,Human_RBP_ID_4036547,Human_RBP_ID_5789430,Human_RBP_ID_8304181,Human_RBP_ID_8966197,Human_RBP_ID_10865003,Human_RBP_ID_17456197,Human_RBP_ID_17677171,Human_RBP_ID_17764634,Human_RBP_ID_18568271,Human_RBP_ID_22426997,Human_RBP_ID_22487498,Human_RBP_ID_22531925,Human_RBP_ID_22783149,Human_RBP_ID_23122353,Human_RBP_ID_23205017,Human_RBP_ID_23377221,Human_RBP_ID_26797890,Human_RBP_ID_26858334,Human_RBP_ID_27178971 Human_Splice_Rec_30289,Human_Splice_Rec_30299,Human_Splice_Rec_30307,Human_Splice_Rec_30317,Human_Splice_Rec_30325,Human_Splice_Rec_30333 Human_miRNA_ID_2216576,Human_miRNA_ID_2216577,Human_miRNA_ID_2671494,Human_miRNA_ID_2671495 RMVar_hsa_circ_89818,RMVar_hsa_circ_86114,RMVar_hsa_circ_122043,RMVar_hsa_circ_106898,RMVar_hsa_circ_130480,RMVar_hsa_circ_130481,RMVar_hsa_circ_130482,RMVar_hsa_circ_92739,RMVar_hsa_circ_368746,RMVar_hsa_circ_130484,RMVar_hsa_circ_67667,RMVar_hsa_circ_130485,RMVar_hsa_circ_130483,RMVar_hsa_circ_378859 110584 RMVar_ID_110584 Human_SNP_ID_802574058 m1A Human chr1 + 119741862 119741862 119741862 AGGCTTCCAAGCAGGCGGATGTGAACTTGGTGAACGCTAAGCTGCTGGTGAAAGAGGCTGGCCTC AGGCTTCCAAGCAGGCGGATGTGAACTTGGTGTACGCTAAGCTGCTGGTGAAAGAGGCTGGCCTC A T PHGDH Ensembl:ENSG00000092621 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA chr1:119741733..119741949 31548705,26863196 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_323562,Human_RBP_ID_1344435,Human_RBP_ID_1409767,Human_RBP_ID_1723794,Human_RBP_ID_5680472,Human_RBP_ID_8282965,Human_RBP_ID_8733699,Human_RBP_ID_10550814,Human_RBP_ID_22429617,Human_RBP_ID_23327336 Human_Splice_Rec_115152,Human_Splice_Rec_115153,Human_Splice_Rec_115190,Human_Splice_Rec_115191,Human_Splice_Rec_115220,Human_Splice_Rec_115221,Human_Splice_Rec_115244,Human_Splice_Rec_115245,Human_Splice_Rec_115308,Human_Splice_Rec_115342,Human_Splice_Rec_115343,Human_Splice_Rec_115408,Human_Splice_Rec_115409,Human_Splice_Rec_115434,Human_Splice_Rec_115435,Human_Splice_Rec_115506,Human_Splice_Rec_115507,Human_Splice_Rec_115536,Human_Splice_Rec_115537,Human_Splice_Rec_115558,Human_Splice_Rec_115559,Human_Splice_Rec_115578,Human_Splice_Rec_115579,Human_Splice_Rec_115610,Human_Splice_Rec_115611,Human_Splice_Rec_115614,Human_Splice_Rec_115615 110585 RMVar_ID_110585 Human_SNP_ID_802576667 m1A Human chr1 - 180258210 180258210 180258210 AGGGGGACACCCCTGGACCCCTCCCCCTCAGCACTTCCTTCCCTGCTCCACAGCACTCATCTCAG AGGGGGACACCCCTGGACCCCTCCCCCTCAGCGCTTCCTTCCCTGCTCCACAGCACTCATCTCAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:180258205..180258342 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110586 RMVar_ID_110586 Human_SNP_ID_802587471 m1A Human chr1 - 1339805 1339805 1339805 ACCACCCTAATCCCCACCCCTGCAGGTGAATGACGTGAACTTTGAGAACATGAGCAATGACGATG ACCACCCTAATCCCCACCCCTGCAGGTGAATGGCGTGAACTTTGAGAACATGAGCAATGACGATG T C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1339699..1339811 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 6 brain Human_RBP_ID_1724071,Human_RBP_ID_10554171,Human_RBP_ID_19033559,Human_RBP_ID_23328217 Human_Splice_Rec_3544,Human_Splice_Rec_3545,Human_Splice_Rec_3572,Human_Splice_Rec_3573,Human_Splice_Rec_3610,Human_Splice_Rec_3611,Human_Splice_Rec_3624,Human_Splice_Rec_3625,Human_Splice_Rec_3634 RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_32455,RMVar_hsa_circ_128317,RMVar_hsa_circ_23178 110587 RMVar_ID_110587 Human_SNP_ID_802587779 m1A Human chr1 + 39424162 39424162 39424162 ATCACTGGACAGCTGGAGAGTCTTGAAAGTAGATGGACTGAACTACTCAGTAAGGCAGCAGCCAG ATCACTGGACAGCTGGAGAGTCTTGAAAGTAGCTGGACTGAACTACTCAGTAAGGCAGCAGCCAG A C MACF1 Ensembl:ENSG00000127603 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:39422875..39427513 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 5 haematopoietic and lymphoid tissue Human_RBP_ID_1268,Human_RBP_ID_1747605,Human_RBP_ID_3312570,Human_RBP_ID_5518904,Human_RBP_ID_5537810,Human_RBP_ID_8749068,Human_RBP_ID_9356130,Human_RBP_ID_10978173,Human_RBP_ID_18965272,Human_RBP_ID_22863570,Human_RBP_ID_27797894 Human_Splice_Rec_49941,Human_Splice_Rec_50139,Human_Splice_Rec_50321,Human_Splice_Rec_50655,Human_Splice_Rec_50865,Human_Splice_Rec_51233,Human_Splice_Rec_51361,Human_Splice_Rec_51449 Human_miRNA_ID_2655894 RMVar_hsa_circ_75558,RMVar_hsa_circ_123729,RMVar_hsa_circ_131825,RMVar_hsa_circ_118806,RMVar_hsa_circ_131828,RMVar_hsa_circ_98617,RMVar_hsa_circ_131834,RMVar_hsa_circ_90817,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_93350,RMVar_hsa_circ_131865,RMVar_hsa_circ_110152,RMVar_hsa_circ_25095,RMVar_hsa_circ_131868,RMVar_hsa_circ_124577,RMVar_hsa_circ_131874,RMVar_hsa_circ_127892,RMVar_hsa_circ_131896,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131907,RMVar_hsa_circ_79999,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_131913,RMVar_hsa_circ_82012,RMVar_hsa_circ_131919,RMVar_hsa_circ_131923,RMVar_hsa_circ_353539,RMVar_hsa_circ_363160,RMVar_hsa_circ_365402,RMVar_hsa_circ_358141,RMVar_hsa_circ_328378,RMVar_hsa_circ_344981,RMVar_hsa_circ_307196,RMVar_hsa_circ_46926,RMVar_hsa_circ_59742,RMVar_hsa_circ_131925,RMVar_hsa_circ_12172,RMVar_hsa_circ_131924,RMVar_hsa_circ_40035,RMVar_hsa_circ_29085,RMVar_hsa_circ_307253,RMVar_hsa_circ_82889,RMVar_hsa_circ_325353,RMVar_hsa_circ_62399,RMVar_hsa_circ_131927 110588 RMVar_ID_110588 Human_SNP_ID_802603028 m1A Human chr1 + 155015196 155015196 155015196 AGCCACGGCCTCTGGAGTTCCCAATGGTGAAGACAGTCCTCCACAGGTGCCCCTCCCACCACCTC AGCCACGGCCTCTGGAGTTCCCAATGGTGAAGGCAGTCCTCCACAGGTGCCCCTCCCACCACCTC A G ZBTB7B Ensembl:ENSG00000160685 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155015145..155015350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 6 ovary Human_RBP_ID_22023868 Human_miRNA_ID_873186,Human_miRNA_ID_1231018 110589 RMVar_ID_110589 Human_SNP_ID_802616058 m1A Human chr1 - 206593669 206593669 206593669 CAATCCTGCCCCTGGGGCCAAGGACAGCCTTCAGGTGCAGATCCAGGGAAACCAGGTCCACCACC CAATCCTGCCCCTGGGGCCAAGGACAGCCTTCGGGTGCAGATCCAGGGAAACCAGGTCCACCACC T C EIF2D Ensembl:ENSG00000143486 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:206593601..206593750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_26801463 Human_Splice_Rec_181035,Human_Splice_Rec_181063 Human_miRNA_ID_2749987 RMVar_hsa_circ_26395,RMVar_hsa_circ_366414,RMVar_hsa_circ_339284,RMVar_hsa_circ_139251 110590 RMVar_ID_110590 Human_SNP_ID_802622660 m1A Human chr1 - 154207563 154207563 154207563 ACCTAACTCAGTCCCCTGAGGTCTCCCCAACAACCATCCAGGTGACATACCTCCCCTCCAGTCAG ACCTAACTCAGTCCCCTGAGGTCTCCCCAACACCCATCCAGGTGACATACCTCCCCTCCAGTCAG T G C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154207384..154207647 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_327294,Human_RBP_ID_1726034,Human_RBP_ID_8956340,Human_RBP_ID_17212615,Human_RBP_ID_17330465,Human_RBP_ID_17456549,Human_RBP_ID_17726378,Human_RBP_ID_18187273,Human_RBP_ID_26801039 Human_Splice_Rec_133788,Human_Splice_Rec_133800,Human_Splice_Rec_133814,Human_Splice_Rec_133822,Human_Splice_Rec_133832,Human_Splice_Rec_133842,Human_Splice_Rec_133852,Human_Splice_Rec_133854,Human_Splice_Rec_133858 Human_miRNA_ID_119,Human_miRNA_ID_3774,Human_miRNA_ID_7461,Human_miRNA_ID_11013,Human_miRNA_ID_18202,Human_miRNA_ID_21833,Human_miRNA_ID_25475,Human_miRNA_ID_1956129 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 110591 RMVar_ID_110591 Human_SNP_ID_802624606 m1A Human chr1 - 789860 789856 789861 CCGTTCCATTCCTTTCGGTTCCATTCCATTCGAGTCCATTCCATTCCATTCCATCCCATTCGAGT CCGTTCCATTCCTTTCGGTTCCATTCCATTC_____CATTCCATTCCATTCCATCCCATTCGAGT GGACTC G AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:789809..790059 26863196 MeRIP-seq:(Medium) rs1290262092 Functional Loss DEL ICGC 32..36 33 PBCA 1 - Human_RBP_ID_5092230 110592 RMVar_ID_110592 Human_SNP_ID_802630658 m1A Human chr1 - 45332073 45332073 45332073 TCAACCCTGTGCCTCTCAGGTGGAGCAGGAACAGCTCTTAGCCTCAGGGAGCCTGTCGGGCAGTC TCAACCCTGTGCCTCTCAGGTGGAGCAGGAACTGCTCTTAGCCTCAGGGAGCCTGTCGGGCAGTC T A MUTYH,AL451136.1 Ensembl:ENSG00000132781,Ensembl:ENSG00000288208 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:45332011..45332399 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 15 head and neck Human_Splice_Rec_63012,Human_Splice_Rec_63013,Human_Splice_Rec_63040,Human_Splice_Rec_63041,Human_Splice_Rec_63068,Human_Splice_Rec_63069,Human_Splice_Rec_63096,Human_Splice_Rec_63097,Human_Splice_Rec_63124,Human_Splice_Rec_63125,Human_Splice_Rec_63152,Human_Splice_Rec_63153,Human_Splice_Rec_63180,Human_Splice_Rec_63181,Human_Splice_Rec_63208,Human_Splice_Rec_63209,Human_Splice_Rec_63236,Human_Splice_Rec_63237,Human_Splice_Rec_63264,Human_Splice_Rec_63265,Human_Splice_Rec_63292,Human_Splice_Rec_63293,Human_Splice_Rec_63330,Human_Splice_Rec_63331,Human_Splice_Rec_63360,Human_Splice_Rec_63361,Human_Splice_Rec_63372,Human_Splice_Rec_63373,Human_Splice_Rec_63388,Human_Splice_Rec_63389,Human_Splice_Rec_63402,Human_Splice_Rec_63403,Human_Splice_Rec_63430,Human_Splice_Rec_63431,Human_Splice_Rec_63454,Human_Splice_Rec_63455,Human_Splice_Rec_63482,Human_Splice_Rec_63483,Human_Splice_Rec_63504,Human_Splice_Rec_63526,Human_Splice_Rec_63527,Human_Splice_Rec_63538,Human_Splice_Rec_63539,Human_Splice_Rec_63548,Human_Splice_Rec_63550,Human_Splice_Rec_63551,Human_Splice_Rec_63568,Human_Splice_Rec_63586,Human_Splice_Rec_63748,Human_Splice_Rec_63749 RMVar_hsa_circ_7752,RMVar_hsa_circ_307414,RMVar_hsa_circ_132491,RMVar_hsa_circ_132492,RMVar_hsa_circ_132493 110593 RMVar_ID_110593 Human_SNP_ID_802636930 m1A Human chr1 - 20652339 20652339 20652339 GAGCCCTCTCCGCACAGCGTGGAGACGGGGCAAGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT GAGCCCTCTCCGCACAGCGTGGAGACGGGGCAGGGAGGGGGGTTATTAGGATTGGTGGTTTTGTT T C DDOST Ensembl:ENSG00000244038 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6893 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_RBP_ID_746815,Human_RBP_ID_5746271,Human_RBP_ID_9352482,Human_RBP_ID_17646103,Human_RBP_ID_26375074 Clinvar_Rec_233,Clinvar_Rec_234,Clinvar_Rec_235,Clinvar_Rec_236 GWAS_ID_7731,GWAS_ID_7732,GWAS_ID_7733,GWAS_ID_7734,GWAS_ID_7735,GWAS_ID_7736,GWAS_ID_7737,GWAS_ID_7738,GWAS_ID_7739,GWAS_ID_7740,GWAS_ID_7741,GWAS_ID_7742,GWAS_ID_7743,GWAS_ID_7744,GWAS_ID_7745,GWAS_ID_7746,GWAS_ID_7747,GWAS_ID_7748,GWAS_ID_7749 110594 RMVar_ID_110594 Human_SNP_ID_802647672 m1A Human chr1 + 154974760 154974760 154974760 CTAGCAAACCGAGCGATCATGTCGCACAAACAAATTTACTATTCGGACAAATACGACGACGAGGA CTAGCAAACCGAGCGATCATGTCGCACAAACACATTTACTATTCGGACAAATACGACGACGAGGA A C CKS1B Ensembl:ENSG00000173207 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:154974651..154974852 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 9 uterus,large intestine Human_RBP_ID_1726341,Human_RBP_ID_4074453 Human_Splice_Rec_135555,Human_Splice_Rec_135559 RMVar_hsa_circ_98035,RMVar_hsa_circ_136483 110595 RMVar_ID_110595 Human_SNP_ID_802648220 m1A Human chr1 - 86914731 86914731 86914731 GCTCTCGCCTCCCTCTACTGCCTCAGTCCCCGACCCCCGCGCCCGCCTGCTTGCCCGCCTCCCTC GCTCTCGCCTCCCTCTACTGCCTCAGTCCCCGCCCCCCGCGCCCGCCTGCTTGCCCGCCTCCCTC T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:86914638..86914900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - 110596 RMVar_ID_110596 Human_SNP_ID_802654274 m1A Human chr1 - 41545122 41545117 41545123 TGGTGTTGGTGGTGATGGTGGTAGTGGTGATGATGGTAGTGGTGGTGGTGGTGATGGTAGCGATG TGGTGTTGGTGGTGATGGTGGTAGTGGTGAT______AGTGGTGGTGGTGGTGATGGTAGCGATG TACCATC T HIVEP3 Ensembl:ENSG00000127124 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:41545044..41545367 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..37 33 PAAD 1 - RMVar_hsa_circ_15419 110597 RMVar_ID_110597 Human_SNP_ID_802669722 m1A Human chr1 + 212791738 212791738 212791738 CCGCGAGCTCCTTGTCCCATGGAGGGTCAAGGACCACCAACTCAGGAGACCCCGCCATTTTTCGT CCGCGAGCTCCTTGTCCCATGGAGGGTCAAGGTCCACCAACTCAGGAGACCCCGCCATTTTTCGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212791601..212791775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mantle_cell_lymphoma 3 haematopoietic and lymphoid tissue 110598 RMVar_ID_110598 Human_SNP_ID_802671221 m1A Human chr1 + 11675727 11675727 11675727 GCTTCTCTCGTGTGCACCAGGACTGTGAAGGTACAGCCTGGAGAGGCAAGAGGTTGGTGGAGGCT GCTTCTCTCGTGTGCACCAGGACTGTGAAGGTGCAGCCTGGAGAGGCAAGAGGTTGGTGGAGGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:11675676..11675750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine 110599 RMVar_ID_110599 Human_SNP_ID_802677777 m1A Human chr1 - 204455914 204455914 204455914 ATGACCTGGTCCAGGAGGCCTGCCATTTCGCCAGGTCCCTGGCCTTCACTGTCTATGCCACCCAC ATGACCTGGTCCAGGAGGCCTGCCATTTCGCCTGGTCCCTGGCCTTCACTGTCTATGCCACCCAC T A PIK3C2B Ensembl:ENSG00000133056 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:204455851..204455925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_177367,Human_Splice_Rec_177433,Human_Splice_Rec_177483 RMVar_hsa_circ_88342,RMVar_hsa_circ_101510,RMVar_hsa_circ_139131,RMVar_hsa_circ_61272,RMVar_hsa_circ_139134,RMVar_hsa_circ_265937,RMVar_hsa_circ_9781,RMVar_hsa_circ_44793,RMVar_hsa_circ_37088,RMVar_hsa_circ_328652,RMVar_hsa_circ_46612,RMVar_hsa_circ_19419 110600 RMVar_ID_110600 Human_SNP_ID_802693298 m1A Human chr1 + 145849624 145849609 145849624 GGGAGCTCCCCAGCGTGGGGGCCAGTGGGCCCAGAAAGTGAGAAGGGGTCCCTCGGTACTGGAAG GGGAGCTCCCCAGCGTGG_______________GAAAGTGAGAAGGGGTCCCTCGGTACTGGAAG GGGGCCAGTGGGCCCA G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:145849512..145849661 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 19..33 33 BRCA 1 - Human_miRNA_ID_2660898,Human_miRNA_ID_2660899,Human_miRNA_ID_2679351,Human_miRNA_ID_2679352 RMVar_hsa_circ_135812,RMVar_hsa_circ_135820,RMVar_hsa_circ_135822,RMVar_hsa_circ_135813,RMVar_hsa_circ_100723,RMVar_hsa_circ_125752,RMVar_hsa_circ_135811,RMVar_hsa_circ_120514,RMVar_hsa_circ_76044,RMVar_hsa_circ_92509 110601 RMVar_ID_110601 Human_SNP_ID_802726657 m1A Human chr1 + 1336395 1336395 1336395 GGCCGGCCGGACGCTCTCGCCAGCTGCTCCCCACCCCACTCGGTGCCGTGTGATCCGATTCACTG GGCCGGCCGGACGCTCTCGCCAGCTGCTCCCCCCCCCACTCGGTGCCGTGTGATCCGATTCACTG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:1336344..1336535 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 110602 RMVar_ID_110602 Human_SNP_ID_802730726 m1A Human chr1 + 156742401 156742401 156742401 AGAAATGACACTGGAAGGAACATCAAAGCCCCAGCTACAAAAAGAAAGTCATCAAGCCCCAAATA AGAAATGACACTGGAAGGAACATCAAAGCCCCGGCTACAAAAAGAAAGTCATCAAGCCCCAAATA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156742351..156742550 26863196 MeRIP-seq:(Medium) rs1480491399 Functional Loss SNV ICGC 33..33 33 LICA 1 - 110603 RMVar_ID_110603 Human_SNP_ID_802740250 m1A Human chr1 - 77949280 77949280 77949280 TTTTTTTCAAAGGTCAGGCAGTTCCTGCTCCGACTGGGGCTCCTCCAGGTGGTCAGCCAGATTAT TTTTTTTCAAAGGTCAGGCAGTTCCTGCTCCGGCTGGGGCTCCTCCAGGTGGTCAGCCAGATTAT T C FUBP1 Ensembl:ENSG00000162613 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:77949232..77955336 32194978 MeRIP-seq:(Medium) rs587778376 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,skin squamous_cell_carcinoma 4 skin,stomach Human_RBP_ID_222725,Human_RBP_ID_363020,Human_RBP_ID_743884,Human_RBP_ID_803180,Human_RBP_ID_859231,Human_RBP_ID_5866829,Human_RBP_ID_11113707,Human_RBP_ID_17758293,Human_RBP_ID_24454344,Human_RBP_ID_24556202,Human_RBP_ID_24745631 Human_Splice_Rec_88964,Human_Splice_Rec_88974,Human_Splice_Rec_89012,Human_Splice_Rec_89050,Human_Splice_Rec_89086,Human_Splice_Rec_89090 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_82921,RMVar_hsa_circ_125144,RMVar_hsa_circ_134156,RMVar_hsa_circ_134157,RMVar_hsa_circ_23823,RMVar_hsa_circ_40163,RMVar_hsa_circ_134158,RMVar_hsa_circ_103531,RMVar_hsa_circ_26413,RMVar_hsa_circ_119407,RMVar_hsa_circ_134159,RMVar_hsa_circ_312576,RMVar_hsa_circ_353103,RMVar_hsa_circ_366229,RMVar_hsa_circ_373357,RMVar_hsa_circ_366532,RMVar_hsa_circ_363901,RMVar_hsa_circ_318826,RMVar_hsa_circ_110758,RMVar_hsa_circ_297447,RMVar_hsa_circ_52533,RMVar_hsa_circ_134161,RMVar_hsa_circ_134163,RMVar_hsa_circ_21504,RMVar_hsa_circ_134164,RMVar_hsa_circ_134162 110604 RMVar_ID_110604 Human_SNP_ID_802742381 m1A Human chr1 + 156592332 156592332 156592332 AGCTGGGCCAATATGGTCTATTACCGCCTGAAACCCCGCCGAACCACCCTTGACTCTGCCTTCAG AGCTGGGCCAATATGGTCTATTACCGCCTGAACCCCCGCCGAACCACCCTTGACTCTGCCTTCAG A C NAXE Ensembl:ENSG00000163382 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156592330..156592576 26863196 MeRIP-seq:(Medium) rs1025418049 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_5338617,Human_RBP_ID_22469497 RMVar_hsa_circ_117354,RMVar_hsa_circ_136880 110605 RMVar_ID_110605 Human_SNP_ID_802754371 m1A Human chr1 - 6554274 6554274 6554274 CCCGCCAGGTGTCGCGCGCGGCGGCGGCCCGGAGACCCAACACCGCGACCCCCAGCCCGATCCCT CCCGCCAGGTGTCGCGCGCGGCGGCGGCCCGGTGACCCAACACCGCGACCCCCAGCCCGATCCCT T A NOL9 Ensembl:ENSG00000162408 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:6554227..6554385;chr1:6554197..6554291;chr1:6554224..6554449;chr1:6554233..6554418 26863196,26863410,26863196,26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_17762294 RMVar_hsa_circ_91784,RMVar_hsa_circ_128647 110606 RMVar_ID_110606 Human_SNP_ID_802767106 m1A Human chr1 + 23559221 23559221 23559221 GGTCGAGAATGTAGTCGATGACGCGCTGTAGGATTTCCACCTGGCTAAGCTGAGTGCCTCTCGGG GGTCGAGAATGTAGTCGATGACGCGCTGTAGGGTTTCCACCTGGCTAAGCTGAGTGCCTCTCGGG A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23559075..23559500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 3 haematopoietic and lymphoid tissue 110607 RMVar_ID_110607 Human_SNP_ID_802770917 m1A Human chr1 - 145927060 145927060 145927060 CTTCTGGGGTTCCAGAGAGCATTCACAAACTGAAAGAAAAAGCGAAGAAACGGAAGGGTCGCGGC CTTCTGGGGTTCCAGAGAGCATTCACAAACTGGAAGAAAAAGCGAAGAAACGGAAGGGTCGCGGC T C RBM8A Ensembl:ENSG00000265241 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:145926880..145927100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_855112,Human_RBP_ID_4080432,Human_RBP_ID_5136337,Human_RBP_ID_5331874,Human_RBP_ID_9356738,Human_RBP_ID_18415041,Human_RBP_ID_18968772,Human_RBP_ID_22429625,Human_RBP_ID_22871370,Human_RBP_ID_23329143,Human_RBP_ID_24541825,Human_RBP_ID_26309796 Human_Splice_Rec_118872,Human_Splice_Rec_118873,Human_Splice_Rec_118882,Human_Splice_Rec_118883,Human_Splice_Rec_118894,Human_Splice_Rec_118895,Human_Splice_Rec_118904,Human_Splice_Rec_118908,Human_Splice_Rec_118914 RMVar_hsa_circ_49099 110608 RMVar_ID_110608 Human_SNP_ID_802779538 m1A Human chr1 + 171540553 171540553 171540553 AAAAAACCTGTACTTAGAGATATGAAAGAGGAACGGGAACAGAGGAAGGAGAAAGAAGGAGAAAA AAAAAACCTGTACTTAGAGATATGAAAGAGGATCGGGAACAGAGGAAGGAGAAAGAAGGAGAAAA A T PRRC2C Ensembl:ENSG00000117523 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:171540502..171540675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_18753,Human_RBP_ID_1729121,Human_RBP_ID_5544802,Human_RBP_ID_5712667,Human_RBP_ID_8228062,Human_RBP_ID_8737887,Human_RBP_ID_9466668,Human_RBP_ID_10652631,Human_RBP_ID_17675686,Human_RBP_ID_22131172,Human_RBP_ID_22781138,Human_RBP_ID_22850066,Human_RBP_ID_24754221,Human_RBP_ID_26312191 RMVar_hsa_circ_3751,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_58235,RMVar_hsa_circ_137539,RMVar_hsa_circ_97212,RMVar_hsa_circ_356800,RMVar_hsa_circ_137544,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_366300,RMVar_hsa_circ_373034,RMVar_hsa_circ_137543,RMVar_hsa_circ_373292,RMVar_hsa_circ_369535,RMVar_hsa_circ_361698,RMVar_hsa_circ_364102,RMVar_hsa_circ_360353,RMVar_hsa_circ_122977,RMVar_hsa_circ_319804,RMVar_hsa_circ_137547,RMVar_hsa_circ_137549,RMVar_hsa_circ_118603,RMVar_hsa_circ_137550,RMVar_hsa_circ_137548,RMVar_hsa_circ_137546,RMVar_hsa_circ_62551,RMVar_hsa_circ_120034,RMVar_hsa_circ_137551 110609 RMVar_ID_110609 Human_SNP_ID_802793942 m1A Human chr1 - 156009550 156009550 156009550 CAGCAAGAGGAAATATGACACTCCCAAAACGAAGAAGAACTGATTGGGGCTTCCACAGCCCTCCT CAGCAAGAGGAAATATGACACTCCCAAAACGAGGAAGAACTGATTGGGGCTTCCACAGCCCTCCT T C SSR2 Ensembl:ENSG00000163479 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156009526..156009550 26863196 MeRIP-seq:(Medium) rs200258821 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22873,Human_RBP_ID_1413159,Human_RBP_ID_1726802,Human_RBP_ID_3282961,Human_RBP_ID_8287046,Human_RBP_ID_18187296,Human_RBP_ID_18553063,Human_RBP_ID_19199620,Human_RBP_ID_22429721,Human_RBP_ID_22749481,Human_RBP_ID_26843601 Human_miRNA_ID_3003059 RMVar_hsa_circ_77498,RMVar_hsa_circ_87891,RMVar_hsa_circ_120703,RMVar_hsa_circ_136754,RMVar_hsa_circ_136755,RMVar_hsa_circ_136753 110610 RMVar_ID_110610 Human_SNP_ID_802809944 m1A Human chr1 - 8360707 8360707 8360707 TGGCCATGCCCCACATCAAGCCCCCGCCTACCACTCCCATCCCCCAGCTGCCGGCGCCACAGGCC TGGCCATGCCCCACATCAAGCCCCCGCCTACCCCTCCCATCCCCCAGCTGCCGGCGCCACAGGCC T G RERE Ensembl:ENSG00000142599 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:8360497..8360829 26863196 MeRIP-seq:(Medium) rs1168686058 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5125133,Human_RBP_ID_17070987,Human_RBP_ID_17337933,Human_RBP_ID_18929204 RMVar_hsa_circ_128715,RMVar_hsa_circ_94155,RMVar_hsa_circ_114520,RMVar_hsa_circ_110315,RMVar_hsa_circ_128717,RMVar_hsa_circ_128716 110611 RMVar_ID_110611 Human_SNP_ID_802825306 m1A Human chr1 + 108699518 108699518 108699518 CTATGATAAGGAAAGAGGAAATGAACGAGAAAAAGAGAGAGAGCGATCAAGAGAAAGGTCCAAGG CTATGATAAGGAAAGAGGAAATGAACGAGAAAGAGAGAGAGAGCGATCAAGAGAAAGGTCCAAGG A G PRPF38B Ensembl:ENSG00000134186 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:108699335..108699680 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_531,Human_RBP_ID_190433,Human_RBP_ID_5665041,Human_RBP_ID_10503080,Human_RBP_ID_22520367,Human_RBP_ID_23320326 110612 RMVar_ID_110612 Human_SNP_ID_802839086 m1A Human chr1 - 31059253 31059253 31059253 GGGAGGAGGAAGTGGAGGAGGCGGCTATAATAATAGCAAACATCGATGGCCTACTGGGGATAACA GGGAGGAGGAAGTGGAGGAGGCGGCTATAATACTAGCAAACATCGATGGCCTACTGGGGATAACA T G PUM1 Ensembl:ENSG00000134644 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:31007081..31059327;chr1:31007081..31059300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 mouth squamous_cell_carcinoma,RECA,large_intestine adenocarcinoma 22 head and neck,large intestine Human_RBP_ID_1745213,Human_RBP_ID_2142794,Human_RBP_ID_3309718,Human_RBP_ID_3933136,Human_RBP_ID_4093894,Human_RBP_ID_5518753,Human_RBP_ID_9562932,Human_RBP_ID_10930842,Human_RBP_ID_17748457,Human_RBP_ID_18430141,Human_RBP_ID_18967797,Human_RBP_ID_22874839,Human_RBP_ID_24763952,Human_RBP_ID_26310720,Human_RBP_ID_26861953,Human_RBP_ID_27797707 Human_Splice_Rec_39917,Human_Splice_Rec_39951,Human_Splice_Rec_39993,Human_Splice_Rec_40035,Human_Splice_Rec_40075,Human_Splice_Rec_40149,Human_Splice_Rec_40191,Human_Splice_Rec_40233,Human_Splice_Rec_40359,Human_Splice_Rec_40371 Human_miRNA_ID_1976370,Human_miRNA_ID_1976371 RMVar_hsa_circ_83915,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_131001,RMVar_hsa_circ_53855,RMVar_hsa_circ_82449,RMVar_hsa_circ_118532,RMVar_hsa_circ_131026,RMVar_hsa_circ_131027,RMVar_hsa_circ_116734,RMVar_hsa_circ_355888,RMVar_hsa_circ_131034,RMVar_hsa_circ_131035,RMVar_hsa_circ_64820,RMVar_hsa_circ_329239,RMVar_hsa_circ_131040,RMVar_hsa_circ_41241,RMVar_hsa_circ_298085,RMVar_hsa_circ_131042,RMVar_hsa_circ_131041,RMVar_hsa_circ_271456,RMVar_hsa_circ_131043,RMVar_hsa_circ_271730 110613 RMVar_ID_110613 Human_SNP_ID_802839591 m1A Human chr1 + 31296731 31296731 31296731 TTGACTGGAACCAGCGGCAACTCTGGGCCCTTACGCTTCTGCTGTTCTATCATGGCGGCAACCGG TTGACTGGAACCAGCGGCAACTCTGGGCCCTTTCGCTTCTGCTGTTCTATCATGGCGGCAACCGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr1:31296601..31296800;chr1:31293226..31296800 26863196 MeRIP-seq:(Medium) rs769245953 Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 2 lung 110614 RMVar_ID_110614 Human_SNP_ID_802842017 m1A Human chr1 - 143735935 143735935 143735935 GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGAGCCCATCCAGGGACGCTGATTGCAACTTTTAA GTTCGGCTGTTAACCGAAAGGTTGGTGGTTCGGGCCCATCCAGGGACGCTGATTGCAACTTTTAA T C piR-37182,piR-59260,piR-37183,piR-59259,tRNA-Asn-GTT-6-1,piR-36706,piR-36705 RNACentral:URS00003B4A72,RNACentral:URS00005F0138,RNACentral:URS00003905DB,RNACentral:URS00000E6438,RNACentral:URS00005A1E0D,RNACentral:URS000020012B,RNACentral:URS00004F59A9 piRNA,piRNA,piRNA,piRNA,tRNA,piRNA,piRNA intron,intron,intron,intron,exon,intron,exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_324993,Human_RBP_ID_1410947,Human_RBP_ID_1724735,Human_RBP_ID_5273213,Human_RBP_ID_5432830,Human_RBP_ID_5484236,Human_RBP_ID_5684977,Human_RBP_ID_8240144,Human_RBP_ID_8284271,Human_RBP_ID_8955514,Human_RBP_ID_18524459,Human_RBP_ID_19185928,Human_RBP_ID_22779711,Human_RBP_ID_23121331,Human_RBP_ID_23330044 110615 RMVar_ID_110615 Human_SNP_ID_802849217 m1A Human chr1 + 26864098 26864098 26864098 CTCCAAAGGGCTCCGTGGAGAGGGACTGGCAGAGCTGAGGCCACCTGGGGCTGGGGATCCCACTC CTCCAAAGGGCTCCGTGGAGAGGGACTGGCAGGGCTGAGGCCACCTGGGGCTGGGGATCCCACTC A G SFN Ensembl:ENSG00000175793 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26864047..26864387 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 110616 RMVar_ID_110616 Human_SNP_ID_802861234 m1A Human chr1 + 119623971 119623971 119623971 TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCAGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG TGCTCCTCTTCCTCCTCCAGCCGGTTCTCCCCGGCACTCTCGTCGTCGTCCTCCCGGAGGCTCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119623923..119624034 26863196 MeRIP-seq:(Medium) rs772380695 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 110617 RMVar_ID_110617 Human_SNP_ID_802863979 m1A Human chr1 - 149070991 149070991 149070991 AAATCACATTTGAGGAAGACAAAGTCGACTCAACTCTCATTGGCTCATCCTCTCATGTTGAACGG AAATCACATTTGAGGAAGACAAAGTCGACTCAGCTCTCATTGGCTCATCCTCTCATGTTGAACGG T C NBPF9 Ensembl:ENSG00000269713 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs797023053 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,kidney clear_cell_renal_cell_carcinoma,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,liver hepatocellular_carcinoma 224 biliary tract,kidney,gallbladder,liver,head and neck,prostate,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_2091205 Human_Splice_Rec_124161,Human_Splice_Rec_124209,Human_Splice_Rec_124257,Human_Splice_Rec_124297,Human_Splice_Rec_124331,Human_Splice_Rec_124413,Human_Splice_Rec_124451 RMVar_hsa_circ_12213,RMVar_hsa_circ_60860 110618 RMVar_ID_110618 Human_SNP_ID_802864154 m1A Human chr1 + 154932413 154932413 154932413 AGAGCCGGAGGACAGCACAGACATCAGCTCCAAGTCTGCAGGACAGGGAGATCAGAATCCAGTTA AGAGCCGGAGGACAGCACAGACATCAGCTCCATGTCTGCAGGACAGGGAGATCAGAATCCAGTTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:154932351..154932425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney 110619 RMVar_ID_110619 Human_SNP_ID_802867058 m1A Human chr1 + 227971424 227971424 227971424 AATGGTCTCCGGTCGGTGGGCTCCTCCACGCCAAGCTTGGGCCTCCCGGCGACCTCTGCAGACCC AATGGTCTCCGGTCGGTGGGCTCCTCCACGCCCAGCTTGGGCCTCCCGGCGACCTCTGCAGACCC A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200489028 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110620 RMVar_ID_110620 Human_SNP_ID_802904861 m1A Human chr1 - 156207952 156207952 156207952 GATTGGTGAGGATGGAGGCAGTGGCTGCAGCCAGGGGCCCCGAGACAGCTTGAAAGACAATGTGA GATTGGTGAGGATGGAGGCAGTGGCTGCAGCCGGGGGCCCCGAGACAGCTTGAAAGACAATGTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156207922..156210249 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 110621 RMVar_ID_110621 Human_SNP_ID_802905208 m1A Human chr1 + 21823704 21823704 21823704 CTGACCAGCTCCTCACCGTCGACTTGGATGGAACCTCTGCGGCCCTCCCTGCAGTGGAACTGGGT CTGACCAGCTCCTCACCGTCGACTTGGATGGAGCCTCTGCGGCCCTCCCTGCAGTGGAACTGGGT A G LDLRAD2 Ensembl:ENSG00000187942 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:21823701..21823725 26863196 MeRIP-seq:(Medium) rs1209865019 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 110622 RMVar_ID_110622 Human_SNP_ID_802905716 m1A Human chr1 + 59321577 59321577 59321577 CTGCAATGTCTGGTGGAGAACAGAAACCAGAGAGGTACTATGTGGGTGTGGACGTTGGAACAGGC CTGCAATGTCTGGTGGAGAACAGAAACCAGAGTGGTACTATGTGGGTGTGGACGTTGGAACAGGC A T FGGY Ensembl:ENSG00000172456 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:59321488..59321661 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_359170 Human_Splice_Rec_76988,Human_Splice_Rec_76990,Human_Splice_Rec_77046,Human_Splice_Rec_77054,Human_Splice_Rec_77086,Human_Splice_Rec_77108,Human_Splice_Rec_77138,Human_Splice_Rec_77174,Human_Splice_Rec_77232,Human_Splice_Rec_77270,Human_Splice_Rec_77302,Human_Splice_Rec_77326 RMVar_hsa_circ_281449,RMVar_hsa_circ_341485,RMVar_hsa_circ_65873,RMVar_hsa_circ_133353,RMVar_hsa_circ_100543,RMVar_hsa_circ_125195,RMVar_hsa_circ_133354,RMVar_hsa_circ_7180,RMVar_hsa_circ_14673,RMVar_hsa_circ_299261,RMVar_hsa_circ_280204,RMVar_hsa_circ_354895,RMVar_hsa_circ_361757,RMVar_hsa_circ_68050,RMVar_hsa_circ_55991,RMVar_hsa_circ_364643,RMVar_hsa_circ_365520,RMVar_hsa_circ_75161,RMVar_hsa_circ_358405,RMVar_hsa_circ_358652,RMVar_hsa_circ_358948,RMVar_hsa_circ_350613,RMVar_hsa_circ_299886,RMVar_hsa_circ_334854,RMVar_hsa_circ_339788,RMVar_hsa_circ_330935,RMVar_hsa_circ_287407,RMVar_hsa_circ_297496,RMVar_hsa_circ_283465,RMVar_hsa_circ_48691,RMVar_hsa_circ_102782,RMVar_hsa_circ_280605,RMVar_hsa_circ_69642,RMVar_hsa_circ_133357,RMVar_hsa_circ_133359,RMVar_hsa_circ_133361,RMVar_hsa_circ_133362,RMVar_hsa_circ_133360,RMVar_hsa_circ_133358,RMVar_hsa_circ_133355,RMVar_hsa_circ_133356 110623 RMVar_ID_110623 Human_SNP_ID_802915281 m1A Human chr1 - 52772270 52772270 52772270 TCTGATAGAGAGCCAGATTCACCGTTTGGCTCAATATTATAAGACCAAGCGAGTCCTCCCTCCCA TCTGATAGAGAGCCAGATTCACCGTTTGGCTCGATATTATAAGACCAAGCGAGTCCTCCCTCCCA T C RPS13P2 Ensembl:ENSG00000228929 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879182143 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_miRNA_ID_1866130,Human_miRNA_ID_1866339 110624 RMVar_ID_110624 Human_SNP_ID_802942248 m1A Human chr1 + 44739933 44739933 44739933 TTGCGCGTTTCTCTTCCTTGCTGACTCTCCGAATGGCCATGGACTCGTCGCTTCAGGCCCGCCTG TTGCGCGTTTCTCTTCCTTGCTGACTCTCCGACTGGCCATGGACTCGTCGCTTCAGGCCCGCCTG A C KIF2C Ensembl:ENSG00000142945 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:44739882..44739951 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_356214,Human_RBP_ID_3314233,Human_RBP_ID_5414554,Human_RBP_ID_5458666,Human_RBP_ID_5486417,Human_RBP_ID_5829734,Human_RBP_ID_8312437,Human_RBP_ID_8754960,Human_RBP_ID_9270115,Human_RBP_ID_22023305 Human_Splice_Rec_61957,Human_Splice_Rec_61977,Human_Splice_Rec_61995 110625 RMVar_ID_110625 Human_SNP_ID_802948669 m1A Human chr1 - 44644762 44644762 44644762 TGTGGCTTCCCATACTCCAGAGTGTCATCCCCATCCACATCCAAGTCAGCATCACTGTCCGGGTT TGTGGCTTCCCATACTCCAGAGTGTCATCCCCGTCCACATCCAAGTCAGCATCACTGTCCGGGTT T C TMEM53 Ensembl:ENSG00000126106 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:44644676..44644800;chr1:44644674..44644800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 110626 RMVar_ID_110626 Human_SNP_ID_802957806 m1A Human chr1 + 224189583 224189583 224189583 CCTGTTTTTTTGTTTTTTCTTTACAGCAAAGTATCCAGAGATAAAGTCCTTGATGAAACCTGATC CCTGTTTTTTTGTTTTTTCTTTACAGCAAAGTGTCCAGAGATAAAGTCCTTGATGAAACCTGATC A G DEGS1 Ensembl:ENSG00000143753 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:224189576..224189625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_1421701,Human_RBP_ID_1737529,Human_RBP_ID_4077166,Human_RBP_ID_8299502,Human_RBP_ID_9489770,Human_RBP_ID_10792655,Human_RBP_ID_18563827,Human_RBP_ID_22855187,Human_RBP_ID_27176288 Human_Splice_Rec_190978,Human_Splice_Rec_190982,Human_Splice_Rec_190986,Human_Splice_Rec_190990 RMVar_hsa_circ_139842,RMVar_hsa_circ_270810,RMVar_hsa_circ_139843,RMVar_hsa_circ_139841 110627 RMVar_ID_110627 Human_SNP_ID_802968211 m1A Human chr1 - 100213390 100213390 100213390 AGGAGTAGGGCGGCTGCGGGGGCGCGGCGGGGATGGCGCCGTAGCCGTGCGGGCCTCACGCGTAG AGGAGTAGGGCGGCTGCGGGGGCGCGGCGGGGGTGGCGCCGTAGCCGTGCGGGCCTCACGCGTAG T C DBT Ensembl:ENSG00000137992 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:100213353..100213489;chr1:100213300..100213544 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_27835265 RMVar_hsa_circ_12161,RMVar_hsa_circ_32764,RMVar_hsa_circ_134929,RMVar_hsa_circ_295112,RMVar_hsa_circ_134930,RMVar_hsa_circ_15447,RMVar_hsa_circ_134931,RMVar_hsa_circ_308498,RMVar_hsa_circ_329925,RMVar_hsa_circ_35899,RMVar_hsa_circ_10769 110628 RMVar_ID_110628 Human_SNP_ID_802972296 m1A Human chr1 + 19141483 19141483 19141483 GCCAGCAGGGCCTCCAGGGGAGAGGGGTTGCCATTGTTGACATTTTCAGCTGTCTCCAGGACCAT GCCAGCAGGGCCTCCAGGGGAGAGGGGTTGCCGTTGTTGACATTTTCAGCTGTCTCCAGGACCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19141315..19141546 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung 110629 RMVar_ID_110629 Human_SNP_ID_802984571 m1A Human chr1 - 162069869 162069869 162069869 CGGGCTGCGCGGCGCCCCTGCCCGGGGAGGGGAGCGGTGGGGCTTGCGGCCCGAAGCGGGACTGG CGGGCTGCGCGGCGCCCCTGCCCGGGGAGGGGGGCGGTGGGGCTTGCGGCCCGAAGCGGGACTGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:162069775..162069900 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110630 RMVar_ID_110630 Human_SNP_ID_802990921 m1A Human chr1 + 67791710 67791710 67791710 CATCTCCTCTGCTCCCATCTGGGCAAACTAGCAGCATCTCTCGCCTGGATGACTTAAAGAGTTCC CATCTCCTCTGCTCCCATCTGGGCAAACTAGCTGCATCTCTCGCCTGGATGACTTAAAGAGTTCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:67791707..67792037 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 110631 RMVar_ID_110631 Human_SNP_ID_802993522 m1A Human chr1 - 155763466 155763466 155763466 GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCAGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT GAAGAGAATTCTCAGGAGGAGAACTCTGAGCCGGAAGAAGAGGAGGAAGAAGAAGCAGAAGGAAT T C GON4L Ensembl:ENSG00000116580 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155763424..155763509 26863196 MeRIP-seq:(Medium) rs607834 Functional Loss SNV ICGC,COSMIC 33..33 33 skin seborrhoeic_keratosis,thyroid neoplasm,COCA,oesophagus squamous_cell_carcinoma,liver neoplasm,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,endometrium endometrioid_carcinoma 66 uterus,liver,oesophagus,skin,head and neck,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_5536619,Human_RBP_ID_24541699,Human_RBP_ID_26311926,Human_RBP_ID_27798605 Human_Splice_Rec_140052,Human_Splice_Rec_140114,Human_Splice_Rec_140176,Human_Splice_Rec_140240,Human_Splice_Rec_140302 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668,RMVar_hsa_circ_6614,RMVar_hsa_circ_62122,RMVar_hsa_circ_53480,RMVar_hsa_circ_268558,RMVar_hsa_circ_72995,RMVar_hsa_circ_62364,RMVar_hsa_circ_67549,RMVar_hsa_circ_104870,RMVar_hsa_circ_98494,RMVar_hsa_circ_136689,RMVar_hsa_circ_136690,RMVar_hsa_circ_101015,RMVar_hsa_circ_136691,RMVar_hsa_circ_367638,RMVar_hsa_circ_13676,RMVar_hsa_circ_67152,RMVar_hsa_circ_108586,RMVar_hsa_circ_136692 110632 RMVar_ID_110632 Human_SNP_ID_802994619 m1A Human chr1 - 225567358 225567358 225567358 AGCTGCTGTGATGGTTTATGATGATGCCAATAAGAAGTGGGTGCCAGCTGGTGGCTCAACTGGAT AGCTGCTGTGATGGTTTATGATGATGCCAATATGAAGTGGGTGCCAGCTGGTGGCTCAACTGGAT T A ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:225567307..225567454 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 KICH,kidney chromophobe_renal_cell_carcinoma 4 kidney Human_RBP_ID_21795,Human_RBP_ID_856943,Human_RBP_ID_1422179,Human_RBP_ID_1738389,Human_RBP_ID_4089790,Human_RBP_ID_9357577,Human_RBP_ID_17676706,Human_RBP_ID_22855986,Human_RBP_ID_23368272,Human_RBP_ID_27176580 Human_Splice_Rec_192582,Human_Splice_Rec_192626,Human_Splice_Rec_192654,Human_Splice_Rec_192698,Human_Splice_Rec_192706 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_365726,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688,RMVar_hsa_circ_285345,RMVar_hsa_circ_140048,RMVar_hsa_circ_140045,RMVar_hsa_circ_140047,RMVar_hsa_circ_292308,RMVar_hsa_circ_375143 110633 RMVar_ID_110633 Human_SNP_ID_803003796 m1A Human chr1 - 215573788 215573788 215573788 GAATCCACATAAGAGTTTGTCTTGAGGTACTAAATCTGCAATTAAAAATCATCTGGTATTATAAG GAATCCACATAAGAGTTTGTCTTGAGGTACTACATCTGCAATTAAAAATCATCTGGTATTATAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:215573776..215573850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary 110634 RMVar_ID_110634 Human_SNP_ID_803010124 m1A Human chr1 + 154963201 154963201 154963201 GCAATCTCTAAGGGTTGCATATCCCCAGGGAGAGGGGACAGCTGCCACTCCTGCCTCTGTTATCC GCAATCTCTAAGGGTTGCATATCCCCAGGGAGGGGGGACAGCTGCCACTCCTGCCTCTGTTATCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:154963151..154963225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110635 RMVar_ID_110635 Human_SNP_ID_803010666 m1A Human chr1 - 111763009 111763009 111763009 ATTATTTTGAAATAATGAAACAGATGAAATGTACCTGGTAAAGGGAGAAGGTTGATATTACATTT ATTATTTTGAAATAATGAAACAGATGAAATGTGCCTGGTAAAGGGAGAAGGTTGATATTACATTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111762849..111765828 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 110636 RMVar_ID_110636 Human_SNP_ID_803010828 m1A Human chr1 - 150223239 150223239 150223239 CAATCTTCAAACTGAATATTTGAATTTCAAGGATGAAGAAGATGATGATGACTATGTTGAAGAAG CAATCTTCAAACTGAATATTTGAATTTCAAGGTTGAAGAAGATGATGATGACTATGTTGAAGAAG T A ANP32E Ensembl:ENSG00000143401 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:150223176..150223250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_21086,Human_RBP_ID_190457,Human_RBP_ID_325346,Human_RBP_ID_1411214,Human_RBP_ID_1724899,Human_RBP_ID_2180491,Human_RBP_ID_3933906,Human_RBP_ID_5686198,Human_RBP_ID_9340454,Human_RBP_ID_9356770,Human_RBP_ID_10567561,Human_RBP_ID_21963146,Human_RBP_ID_22870934,Human_RBP_ID_23112452,Human_RBP_ID_23330706,Human_RBP_ID_24541510,Human_RBP_ID_26309802,Human_RBP_ID_27800731 Human_Splice_Rec_125924,Human_Splice_Rec_125925,Human_Splice_Rec_125932,Human_Splice_Rec_125933,Human_Splice_Rec_125944,Human_Splice_Rec_125945,Human_Splice_Rec_125954,Human_Splice_Rec_125955,Human_Splice_Rec_125958,Human_Splice_Rec_125959,Human_Splice_Rec_125966,Human_Splice_Rec_125967,Human_Splice_Rec_125976,Human_Splice_Rec_125977 RMVar_hsa_circ_368933 110637 RMVar_ID_110637 Human_SNP_ID_803014738 m1A Human chr1 + 2193689 2193689 2193689 TGGCACATGGGGCAGCTGCGCAGGGCCGCGGCACCCTCCACAGACGGCTGCTGCTCCACCCTGGG TGGCACATGGGGCAGCTGCGCAGGGCCGCGGCCCCCTCCACAGACGGCTGCTGCTCCACCCTGGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:2193589..2193921;chr1:2193607..2193942 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 STAD 1 - 110638 RMVar_ID_110638 Human_SNP_ID_803025522 m1A Human chr1 - 67409731 67409731 67409731 CAGCTTCCCAGAAATTTGGGTTATTTGGCCTAAGCTGTGCCCTGGGATTACCTCTTCATCTTCCT CAGCTTCCCAGAAATTTGGGTTATTTGGCCTAGGCTGTGCCCTGGGATTACCTCTTCATCTTCCT T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4655707 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_224013,Human_RBP_ID_979528,Human_RBP_ID_5856297,Human_RBP_ID_8751524,Human_RBP_ID_8973498,Human_RBP_ID_11084570,Human_RBP_ID_23409591,Human_RBP_ID_26382581 Human_miRNA_ID_574253 GWAS_ID_8216,GWAS_ID_8217 110639 RMVar_ID_110639 Human_SNP_ID_803041017 m1A Human chr1 + 21614084 21614084 21614084 CCGAGGGCAGCGTCCAGTGAGTAGTAATTGAAATGCTCCTGCAGTGGGAGGTGGGGGCCAGGGGA CCGAGGGCAGCGTCCAGTGAGTAGTAATTGAAGTGCTCCTGCAGTGGGAGGTGGGGGCCAGGGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:21614037..21614123 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 6 liver 110640 RMVar_ID_110640 Human_SNP_ID_803047962 m1A Human chr1 - 206696095 206696095 206696095 CTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAAGGTGAAGGCAGGTGAGATGAATCCT CTGGCAAAGAAATCATCTGCCGTGTGACTGGTGGGATGAAGGTGAAGGCAGGTGAGATGAATCCT T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879954703 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_miRNA_ID_1839027 110641 RMVar_ID_110641 Human_SNP_ID_803051251 m1A Human chr1 + 220787105 220787105 220787105 ATGGCCCACGCGGCGCCGGCGGCTGCTGCAGCAGGTGGGCACAGTGGCGCAGCTCTGGATCTACC ATGGCCCACGCGGCGCCGGCGGCTGCTGCAGCCGGTGGGCACAGTGGCGCAGCTCTGGATCTACC A C AL445423.3,MTARC1 Ensembl:ENSG00000286231,Ensembl:ENSG00000186205 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:220786926..220787125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_4076385,Human_RBP_ID_17739457,Human_RBP_ID_22428801 110642 RMVar_ID_110642 Human_SNP_ID_803056320 m1A Human chr1 - 45659098 45659098 45659098 AGGTTGGATGCCTCACCTTACTGAAAGGAGACACTGGACCTAAATGGCGCAGCATGATTTTGTTC AGGTTGGATGCCTCACCTTACTGAAAGGAGACGCTGGACCTAAATGGCGCAGCATGATTTTGTTC T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:45659009..45660550 32194978 MeRIP-seq:(Medium) rs1340804810 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_356572,Human_RBP_ID_1432231,Human_RBP_ID_1749077,Human_RBP_ID_4056124,Human_RBP_ID_5414061,Human_RBP_ID_5831175,Human_RBP_ID_8312881,Human_RBP_ID_8749820,Human_RBP_ID_11008075,Human_RBP_ID_17218858,Human_RBP_ID_22870838 Human_Splice_Rec_64602,Human_Splice_Rec_64603,Human_Splice_Rec_64624,Human_Splice_Rec_64625,Human_Splice_Rec_64662 Human_miRNA_ID_2174188,Human_miRNA_ID_2174189,Human_miRNA_ID_2177632,Human_miRNA_ID_2177633 RMVar_hsa_circ_108892,RMVar_hsa_circ_87077,RMVar_hsa_circ_132544,RMVar_hsa_circ_132545,RMVar_hsa_circ_283999,RMVar_hsa_circ_88773,RMVar_hsa_circ_117168,RMVar_hsa_circ_132549,RMVar_hsa_circ_360601,RMVar_hsa_circ_305521,RMVar_hsa_circ_132553,RMVar_hsa_circ_336735,RMVar_hsa_circ_132557,RMVar_hsa_circ_132561,RMVar_hsa_circ_372844,RMVar_hsa_circ_300598,RMVar_hsa_circ_80147,RMVar_hsa_circ_132562,RMVar_hsa_circ_132560,RMVar_hsa_circ_306659,RMVar_hsa_circ_356528,RMVar_hsa_circ_269907,RMVar_hsa_circ_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564,RMVar_hsa_circ_132565 110643 RMVar_ID_110643 Human_SNP_ID_803057560 m1A Human chr1 + 225653011 225653011 225653011 CCTCCTCCCGGAGCTTCCTCGGCCGCCCTCTGAGGGGTGCCCGCCGGGGCCGCGCGCCCGGCCGC CCTCCTCCCGGAGCTTCCTCGGCCGCCCTCTGGGGGGTGCCCGCCGGGGCCGCGCGCCCGGCCGC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:225652912..225653100 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110644 RMVar_ID_110644 Human_SNP_ID_803058964 m1A Human chr1 + 39034445 39034445 39034445 AGGAAGCAGCGGGATAAGCTGATAAAGGAAGGAAAGTACACCCCTCCACCTCACCACATTGGCAA AGGAAGCAGCGGGATAAGCTGATAAAGGAAGGGAAGTACACCCCTCCACCTCACCACATTGGCAA A G NDUFS5 Ensembl:ENSG00000168653 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:39034390..39034491;chr1:39034375..39034536;chr1:39034369..39034468 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_354873,Human_RBP_ID_5109088,Human_RBP_ID_5136208,Human_RBP_ID_17646947,Human_RBP_ID_23393370,Human_RBP_ID_26390940,Human_RBP_ID_26864323 Human_Splice_Rec_49806,Human_Splice_Rec_49810 Human_miRNA_ID_2152694,Human_miRNA_ID_2800565,Human_miRNA_ID_3008693 RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 110645 RMVar_ID_110645 Human_SNP_ID_803071985 m1A Human chr1 - 100133253 100133253 100133253 TCTTTTCCCTGCGGCCACCACCATCCTGCAGAACCGTTTCTTCTTTTCCACATAGTAACCGCATC TCTTTTCCCTGCGGCCACCACCATCCTGCAGAGCCGTTTCTTCTTTTCCACATAGTAACCGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:100133203..100133342 26863196 MeRIP-seq:(Medium) rs757056954 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 110646 RMVar_ID_110646 Human_SNP_ID_803072660 m1A Human chr1 - 116392954 116392954 116392954 GGTACTTGTTGGTGGAGTTGAAGGGTATCTCGACGATTTTGGCGTATCTTTCTCTCATCTCCTTC GGTACTTGTTGGTGGAGTTGAAGGGTATCTCGGCGATTTTGGCGTATCTTTCTCTCATCTCCTTC T C ATP1A1-AS1 Ensembl:ENSG00000203865 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:116392904..116393028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma 3 kidney Human_Splice_Rec_113978 110647 RMVar_ID_110647 Human_SNP_ID_803085839 m1A Human chr1 - 44213759 44213759 44213759 AGTTCTAGAATGTCCCGTACATCCGCGCCCGTAGCCATCGCGCCTGAGAGATGGGGGAGCCACCG AGTTCTAGAATGTCCCGTACATCCGCGCCCGTTGCCATCGCGCCTGAGAGATGGGGGAGCCACCG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:44213559..44213775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110648 RMVar_ID_110648 Human_SNP_ID_803118168 m1A Human chr1 + 151117986 151117986 151117986 CAGGAAGGCAATGAAAGAGAGCTACTACAGCAACAACTCCAGGAGGCCAATCGAAGAGCCCAGGA CAGGAAGGCAATGAAAGAGAGCTACTACAGCAGCAACTCCAGGAGGCCAATCGAAGAGCCCAGGA A G GABPB2 Ensembl:ENSG00000143458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151117958..151118049 26863196 MeRIP-seq:(Medium) rs1264066022 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_Splice_Rec_128296,Human_Splice_Rec_128330,Human_Splice_Rec_128336 RMVar_hsa_circ_19016,RMVar_hsa_circ_288996,RMVar_hsa_circ_267228,RMVar_hsa_circ_136021,RMVar_hsa_circ_340094,RMVar_hsa_circ_300384,RMVar_hsa_circ_136030,RMVar_hsa_circ_136033,RMVar_hsa_circ_136034,RMVar_hsa_circ_330561,RMVar_hsa_circ_309381,RMVar_hsa_circ_136035 110649 RMVar_ID_110649 Human_SNP_ID_803131153 m1A Human chr1 - 153949326 153949326 153949326 GTCCACTGACCAGCGGTTACCCCCATACCCATACAGCTCCCCAAGTCTGGTTCTGCCTACCCAGC GTCCACTGACCAGCGGTTACCCCCATACCCATTCAGCTCCCCAAGTCTGGTTCTGCCTACCCAGC T A CRTC2 Ensembl:ENSG00000160741 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:153949301..153949325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_17071973,Human_RBP_ID_17223499,Human_RBP_ID_17338431,Human_RBP_ID_18552014,Human_RBP_ID_18930006,Human_RBP_ID_27388458 Human_Splice_Rec_132838,Human_Splice_Rec_132858,Human_Splice_Rec_132866,Human_Splice_Rec_132890,Human_Splice_Rec_132910,Human_Splice_Rec_132916 Human_miRNA_ID_690851,Human_miRNA_ID_841220 RMVar_hsa_circ_30288 110650 RMVar_ID_110650 Human_SNP_ID_803133906 m1A Human chr1 + 207331295 207331295 207331295 GGAGAGTGGAGTGGCCCACCACCTGAATGCAGAGGTAATCACTTTGGATAGTTATATTTTTGCTT GGAGAGTGGAGTGGCCCACCACCTGAATGCAGGGGTAATCACTTTGGATAGTTATATTTTTGCTT A G CD55 Ensembl:ENSG00000196352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:207331086..207331336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_2117856,Human_RBP_ID_17221958,Human_RBP_ID_17763094,Human_RBP_ID_22750454,Human_RBP_ID_24626923 Human_Splice_Rec_181865,Human_Splice_Rec_181881,Human_Splice_Rec_181899,Human_Splice_Rec_181919,Human_Splice_Rec_181937,Human_Splice_Rec_181957,Human_Splice_Rec_181973,Human_Splice_Rec_181995,Human_Splice_Rec_182003,Human_Splice_Rec_182013,Human_Splice_Rec_182027,Human_Splice_Rec_182037,Human_Splice_Rec_182047 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296,RMVar_hsa_circ_357447,RMVar_hsa_circ_139298 110651 RMVar_ID_110651 Human_SNP_ID_803134863 m1A Human chr1 + 37978781 37978781 37978781 GGCAAACAAAGAGGTATCAAGTGACTCCAGGGACTTTCCTTTGGTACTGAATAGTCTCTGGGCTC GGCAAACAAAGAGGTATCAAGTGACTCCAGGGCCTTTCCTTTGGTACTGAATAGTCTCTGGGCTC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:37968076..37978814 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - 110652 RMVar_ID_110652 Human_SNP_ID_803137058 m1A Human chr1 + 116390377 116390377 116390377 ATGACAGTGGCCCACATGTGGTTTGACAATCAAATCCATGAAGCTGATACGACAGAGAATCAGAG ATGACAGTGGCCCACATGTGGTTTGACAATCACATCCATGAAGCTGATACGACAGAGAATCAGAG A C ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_22799,Human_RBP_ID_322786,Human_RBP_ID_1409239,Human_RBP_ID_1723208,Human_RBP_ID_17221537,Human_RBP_ID_22749372 Human_Splice_Rec_113827,Human_Splice_Rec_113875,Human_Splice_Rec_113929 RMVar_hsa_circ_12349,RMVar_hsa_circ_358341,RMVar_hsa_circ_374099,RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_85489,RMVar_hsa_circ_78811,RMVar_hsa_circ_135610,RMVar_hsa_circ_135609,RMVar_hsa_circ_135612,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_135614,RMVar_hsa_circ_64344,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_104205,RMVar_hsa_circ_42533,RMVar_hsa_circ_135617,RMVar_hsa_circ_135618,RMVar_hsa_circ_135620,RMVar_hsa_circ_135619,RMVar_hsa_circ_371218 110653 RMVar_ID_110653 Human_SNP_ID_803144903 m1A Human chr1 - 156814009 156814009 156814009 TCTGATCCCTAACGGCGCCCTCCAGGAGCCGGACTTGCTGCCGCCACTTCCTGCTGGCCCAGCTC TCTGATCCCTAACGGCGCCCTCCAGGAGCCGGGCTTGCTGCCGCCACTTCCTGCTGGCCCAGCTC T C SH2D2A Ensembl:ENSG00000027869 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156813974..156814085 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_Splice_Rec_143742,Human_Splice_Rec_143758,Human_Splice_Rec_143774,Human_Splice_Rec_143790 110654 RMVar_ID_110654 Human_SNP_ID_803155668 m1A Human chr1 + 153670931 153670930 153670931 ACCGCTTCGACCCACTTACCTCATGGCGCCTTAAAACACGAACAATGGAGGCCGCACCAACCGCC ACCGCTTCGACCCACTTACCTCATGGCGCCTT_AAACACGAACAATGGAGGCCGCACCAACCGCC TA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:153668526..153671000 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 COAD 1 - 110655 RMVar_ID_110655 Human_SNP_ID_803176019 m1A Human chr1 + 110341295 110341295 110341295 GGTTGGTCCTTGGACCGGGACAGAGGTGATCGAGATCTGCCCAGCAGCAGAGACCAGCCTAGGAA GGTTGGTCCTTGGACCGGGACAGAGGTGATCGGGATCTGCCCAGCAGCAGAGACCAGCCTAGGAA A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:110341187..110341300 32194978 MeRIP-seq:(Medium) rs3738751 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_RBP_ID_5519112,Human_RBP_ID_10513096,Human_RBP_ID_18547123,Human_RBP_ID_22707131,Human_RBP_ID_26311609,Human_RBP_ID_27385687 GWAS_ID_8436,GWAS_ID_8437,GWAS_ID_8438 110656 RMVar_ID_110656 Human_SNP_ID_803184561 m1A Human chr1 + 6554466 6554466 6554466 GGCCTTGCGGACCCGCAGCCAAGTGGAACGGCAGGAACCCCGCTTTAGCAGCAGTCCCGAGTCCG GGCCTTGCGGACCCGCAGCCAAGTGGAACGGCGGGAACCCCGCTTTAGCAGCAGTCCCGAGTCCG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:6554336..6554465 26863196 MeRIP-seq:(Medium) rs12742808 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver 110657 RMVar_ID_110657 Human_SNP_ID_803207263 m1A Human chr1 - 179889371 179889371 179889371 ACAAAGGTAAACCAACAGACAAACAATCTCTTACCATATCTTGGGTATCTTAGAGGGGGTCGACG ACAAAGGTAAACCAACAGACAAACAATCTCTTGCCATATCTTGGGTATCTTAGAGGGGGTCGACG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:179889362..179903980 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 110658 RMVar_ID_110658 Human_SNP_ID_803208848 m1A Human chr1 - 67753901 67753901 67753901 TGGCAGAGTGCTCACATACACTGCCACACTTAACGCCCGCCACCTGTCCTGCTGGGCAGGCATTC TGGCAGAGTGCTCACATACACTGCCACACTTATCGCCCGCCACCTGTCCTGCTGGGCAGGCATTC T A GNG12 Ensembl:ENSG00000172380 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:67753894..67754010 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 110659 RMVar_ID_110659 Human_SNP_ID_803210245 m1A Human chr1 - 12568159 12568159 12568159 AGTCCCAGGACCTTTGCACAGGACTGATGGGTATAACTGACCCCCACAGGGAGGCAGGAAAACAG AGTCCCAGGACCTTTGCACAGGACTGATGGGTGTAACTGACCCCCACAGGGAGGCAGGAAAACAG T C DHRS3 Ensembl:ENSG00000162496 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:12568108..12568358 32194978 MeRIP-seq:(Medium) rs4580 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_1410041,Human_RBP_ID_3988478,Human_RBP_ID_18157477,Human_RBP_ID_22022761,Human_RBP_ID_27554291 Human_miRNA_ID_2244806 GWAS_ID_8029,GWAS_ID_8030,GWAS_ID_8031,GWAS_ID_8032,GWAS_ID_8033 RMVar_hsa_circ_98104,RMVar_hsa_circ_129345 110660 RMVar_ID_110660 Human_SNP_ID_803227502 m1A Human chr1 - 39565227 39565226 39565227 TGTTGCCCTGGCCCAGAGGAAGGAAGAGAGAAAGGCTCACCTGACCAACCAGTATATGCAACGAG TGTTGCCCTGGCCCAGAGGAAGGAAGAGAGAA_GGCTCACCTGACCAACCAGTATATGCAACGAG CT C PABPC4 Ensembl:ENSG00000090621 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:39565176..39565307 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - Human_RBP_ID_1431383,Human_RBP_ID_1747734,Human_RBP_ID_3312682,Human_RBP_ID_4051850,Human_RBP_ID_8310870,Human_RBP_ID_18574659,Human_RBP_ID_22023233,Human_RBP_ID_22558783,Human_RBP_ID_26311056 RMVar_hsa_circ_75969,RMVar_hsa_circ_116806,RMVar_hsa_circ_31319,RMVar_hsa_circ_131960,RMVar_hsa_circ_131961,RMVar_hsa_circ_66255,RMVar_hsa_circ_33954,RMVar_hsa_circ_46272,RMVar_hsa_circ_113925,RMVar_hsa_circ_93050,RMVar_hsa_circ_131965,RMVar_hsa_circ_371868,RMVar_hsa_circ_131966,RMVar_hsa_circ_97399,RMVar_hsa_circ_131967,RMVar_hsa_circ_131968 110661 RMVar_ID_110661 Human_SNP_ID_803229480 m1A Human chr1 - 236012024 236012024 236012024 GGCTGTTTTACAGATGTAGATGAATGCCAGCCAAGCCGATGTCACCCTGACGCCTTCTGCTACAA GGCTGTTTTACAGATGTAGATGAATGCCAGCCCAGCCGATGTCACCCTGACGCCTTCTGCTACAA T G NID1 Ensembl:ENSG00000116962 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:236011926..236012025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_lower_lobe adenocarcinoma,LUAD 4 lung Human_Splice_Rec_202724 Human_miRNA_ID_2721158 RMVar_hsa_circ_67934,RMVar_hsa_circ_120115,RMVar_hsa_circ_86693,RMVar_hsa_circ_140787,RMVar_hsa_circ_140788,RMVar_hsa_circ_118732,RMVar_hsa_circ_140789,RMVar_hsa_circ_118914,RMVar_hsa_circ_73961,RMVar_hsa_circ_140792,RMVar_hsa_circ_368978,RMVar_hsa_circ_10240,RMVar_hsa_circ_273359,RMVar_hsa_circ_15781,RMVar_hsa_circ_13797,RMVar_hsa_circ_335665,RMVar_hsa_circ_360744,RMVar_hsa_circ_303845,RMVar_hsa_circ_73602,RMVar_hsa_circ_103529,RMVar_hsa_circ_26843,RMVar_hsa_circ_140793,RMVar_hsa_circ_6065,RMVar_hsa_circ_140794 110662 RMVar_ID_110662 Human_SNP_ID_803231231 m1A Human chr1 + 16678268 16678268 16678268 AGTAAAGAGCCATAGCGAAGTGAAAAACAACCACGTGCAGTGGCCGGGAATTGAACCCGGGTCTC AGTAAAGAGCCATAGCGAAGTGAAAAACAACCGCGTGCAGTGGCCGGGAATTGAACCCGGGTCTC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:16678259..16678346 26863410 MeRIP-seq:(Medium) rs771367393 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110663 RMVar_ID_110663 Human_SNP_ID_803246998 m1A Human chr1 - 31756049 31756049 31756049 GCCCGGGGGCCCAGCCCCACCTGCTGAGGCCGATTTGCACTCGGGGAGCAGCAATGATCTGTTCA GCCCGGGGGCCCAGCCCCACCTGCTGAGGCCGGTTTGCACTCGGGGAGCAGCAATGATCTGTTCA T C ADGRB2 Ensembl:ENSG00000121753 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:31744250..31756106 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_41695,Human_Splice_Rec_41749,Human_Splice_Rec_41807,Human_Splice_Rec_41865,Human_Splice_Rec_41939,Human_Splice_Rec_42013,Human_Splice_Rec_42067,Human_Splice_Rec_42125,Human_Splice_Rec_42151,Human_Splice_Rec_42167 Human_miRNA_ID_2018346,Human_miRNA_ID_2023441,Human_miRNA_ID_2179684,Human_miRNA_ID_2181789,Human_miRNA_ID_2310062,Human_miRNA_ID_2312082,Human_miRNA_ID_2498171,Human_miRNA_ID_2605953,Human_miRNA_ID_2653857 RMVar_hsa_circ_90613,RMVar_hsa_circ_131113,RMVar_hsa_circ_131116,RMVar_hsa_circ_107525,RMVar_hsa_circ_131114,RMVar_hsa_circ_122293,RMVar_hsa_circ_30044,RMVar_hsa_circ_111378,RMVar_hsa_circ_131118,RMVar_hsa_circ_77531,RMVar_hsa_circ_131120 110664 RMVar_ID_110664 Human_SNP_ID_803249595 m1A Human chr1 + 23392605 23392605 23392605 CACTCCACACATCATACACACACACTCCACACATCATACACACACACACACACTCCACACATCAT CACTCCACACATCATACACACACACTCCACACGTCATACACACACACACACACTCCACACATCAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:23392539..23392650 26863196 MeRIP-seq:(Medium) rs62642604 Functional Loss SNV ICGC 33..33 33 MELA 1 - 110665 RMVar_ID_110665 Human_SNP_ID_803250277 m1A Human chr1 + 120341821 120341821 120341821 TTGAACACATCCCCATTAAATAAGTCCTTGGAAAAGAAGCAGCCGCTATTTCCACCCCACCCCCC TTGAACACATCCCCATTAAATAAGTCCTTGGAGAAGAAGCAGCCGCTATTTCCACCCCACCCCCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:120341770..120341866 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 110666 RMVar_ID_110666 Human_SNP_ID_803256195 m1A Human chr1 - 205810257 205810257 205810257 TGAGTCTCGGGCCAACGCCAAGGGGGTTCGGGAGGAGGACGCCCTGCTGGAGAACGGGAGCCAGA TGAGTCTCGGGCCAACGCCAAGGGGGTTCGGGGGGAGGACGCCCTGCTGGAGAACGGGAGCCAGA T C SLC41A1 Ensembl:ENSG00000133065 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205810210..205810286 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_108516,RMVar_hsa_circ_139241 110667 RMVar_ID_110667 Human_SNP_ID_803266592 m1A Human chr1 - 26780951 26780951 26780951 TGAGGGGAGTAAGGTGAGGACAAGGAACAGAAAGGCGTGAGGTGATGGAGGGAGGGGAGGTGGAA TGAGGGGAGTAAGGTGAGGACAAGGAACAGAACGGCGTGAGGTGATGGAGGGAGGGGAGGTGGAA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:26780926..26780950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 110668 RMVar_ID_110668 Human_SNP_ID_803278537 m1A Human chr1 - 27668508 27668508 27668508 TGCAGGTAAGAAAAAGTGCTCGGAGAGCTCGGACAGCGGCTCCGGGTTCTGGAAGGCCCTGACCT TGCAGGTAAGAAAAAGTGCTCGGAGAGCTCGGGCAGCGGCTCCGGGTTCTGGAAGGCCCTGACCT T C IFI6 Ensembl:ENSG00000126709 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:27668178..27668570 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 6 brain Human_RBP_ID_350649,Human_RBP_ID_4042243 Human_Splice_Rec_36530,Human_Splice_Rec_36531,Human_Splice_Rec_36538,Human_Splice_Rec_36539,Human_Splice_Rec_36546,Human_Splice_Rec_36547 RMVar_hsa_circ_110208,RMVar_hsa_circ_119380,RMVar_hsa_circ_85756,RMVar_hsa_circ_130752,RMVar_hsa_circ_130753,RMVar_hsa_circ_130754,RMVar_hsa_circ_130755,RMVar_hsa_circ_283466 110669 RMVar_ID_110669 Human_SNP_ID_803288209 m1A Human chr1 + 32650499 32650499 32650499 CTTGATCGCCTTCTGTTCTTCAGTCAAATTGTAATCTCTAACATCTTCCTCTTCCTGCGCCATGA CTTGATCGCCTTCTGTTCTTCAGTCAAATTGTCATCTCTAACATCTTCCTCTTCCTGCGCCATGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:32650451..32650525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110670 RMVar_ID_110670 Human_SNP_ID_803288278 m1A Human chr1 + 236900204 236900204 236900204 CTACAGGAAAATAGGTGAATAATTAGATATATATATTCATTCTACGGGATATTATTCAGTAGTGG CTACAGGAAAATAGGTGAATAATTAGATATATGTATTCATTCTACGGGATATTATTCAGTAGTGG A G MTR Ensembl:ENSG00000116984 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9779 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_347687,Human_RBP_ID_2135032,Human_RBP_ID_26390671,Human_RBP_ID_27178886,Human_RBP_ID_27590812 Human_miRNA_ID_149554 Clinvar_Rec_463 110671 RMVar_ID_110671 Human_SNP_ID_803301088 m1A Human chr1 - 211382892 211382892 211382892 GGAAACTGCAGAGAAACAACCTGTTTGGTCCGACTTGACAACCTCAACCGGACCGAAGGTGCTGA GGAAACTGCAGAGAAACAACCTGTTTGGTCCGCCTTGACAACCTCAACCGGACCGAAGGTGCTGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211382847..211382940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 110672 RMVar_ID_110672 Human_SNP_ID_803301089 m1A Human chr1 - 211382892 211382892 211382892 GGAAACTGCAGAGAAACAACCTGTTTGGTCCGACTTGACAACCTCAACCGGACCGAAGGTGCTGA GGAAACTGCAGAGAAACAACCTGTTTGGTCCGGCTTGACAACCTCAACCGGACCGAAGGTGCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211382847..211382940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 110673 RMVar_ID_110673 Human_SNP_ID_803304142 m1A Human chr1 - 21176270 21176270 21176270 GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCAGCGGTACCGCCTCCTCACCCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:21176176..21176375;chr1:21176176..21176350 26863410 MeRIP-seq:(Medium) rs749796228 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,oesophagus adenocarcinoma 5 oesophagus Human_RBP_ID_95834,Human_RBP_ID_5457008 Human_Splice_Rec_26848,Human_Splice_Rec_26849,Human_Splice_Rec_26972,Human_Splice_Rec_26973,Human_Splice_Rec_27040,Human_Splice_Rec_27041,Human_Splice_Rec_27108,Human_Splice_Rec_27109,Human_Splice_Rec_27218,Human_Splice_Rec_27219,Human_Splice_Rec_27236,Human_Splice_Rec_27237,Human_Splice_Rec_27264 RMVar_hsa_circ_125099,RMVar_hsa_circ_129928,RMVar_hsa_circ_130011,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_130010 110674 RMVar_ID_110674 Human_SNP_ID_803311347 m1A Human chr1 - 151600318 151600318 151600318 GGCAGAGGGTTTCCTCACTTCTCAGACGGGGCAGCCGGGCAGAGACGCTCCTCACCTCCCAGACA GGCAGAGGGTTTCCTCACTTCTCAGACGGGGCGGCCGGGCAGAGACGCTCCTCACCTCCCAGACA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:151600295..151600419 26863196 MeRIP-seq:(Medium) rs1407254743 Functional Loss SNV ICGC 33..33 33 LUSC 2 - 110675 RMVar_ID_110675 Human_SNP_ID_803317172 m1A Human chr1 - 209676019 209676019 209676019 CGGTCTGTCTCTGTCTACTGCGTCTCCCTCCCACTCCGCTGGTCTCCCACAGTTCCTAGGAGGCG CGGTCTGTCTCTGTCTACTGCGTCTCCCTCCCCCTCCGCTGGTCTCCCACAGTTCCTAGGAGGCG T G HSD11B1-AS1 Ensembl:ENSG00000227591 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:209675467..209676100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 110676 RMVar_ID_110676 Human_SNP_ID_803319933 m1A Human chr1 - 149887040 149887040 149887040 CGGTGCACTCGCCCTACCGGGAACTGGAGGCCAGCGCGGGACGAGCGCGACTTGGCCTTGGCGCG CGGTGCACTCGCCCTACCGGGAACTGGAGGCCTGCGCGGGACGAGCGCGACTTGGCCTTGGCGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149886989..149887063 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 110677 RMVar_ID_110677 Human_SNP_ID_803328342 m1A Human chr1 + 150344256 150344256 150344256 GAAGCCCACGTCAGAGCTCAGATGGCAAAAAGACAGAAGTAAGTGCCATGGGATTGGGTGGAAAC GAAGCCCACGTCAGAGCTCAGATGGCAAAAAGGCAGAAGTAAGTGCCATGGGATTGGGTGGAAAC A G PRPF3 Ensembl:ENSG00000117360 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:150343449..150344308 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_27798489 Human_Splice_Rec_126264,Human_Splice_Rec_126265,Human_Splice_Rec_126288,Human_Splice_Rec_126289,Human_Splice_Rec_126306 RMVar_hsa_circ_88682,RMVar_hsa_circ_19437,RMVar_hsa_circ_60201,RMVar_hsa_circ_60325,RMVar_hsa_circ_329976,RMVar_hsa_circ_28073,RMVar_hsa_circ_48925,RMVar_hsa_circ_27171,RMVar_hsa_circ_135877,RMVar_hsa_circ_59451 110678 RMVar_ID_110678 Human_SNP_ID_803336098 m1A Human chr1 + 119915441 119915441 119915441 TCTGACCAGTCAGAAGCAGAGTGGGGTGATGAACTTGACCACTGGTCAGGAGACTCTGGGGATGG TCTGACCAGTCAGAAGCAGAGTGGGGTGATGACCTTGACCACTGGTCAGGAGACTCTGGGGATGG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:119915363..119915622 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 110679 RMVar_ID_110679 Human_SNP_ID_803341731 m1A Human chr1 - 1035666 1035666 1035666 CCACCCCTTGCTGAACAGGGAGAAGGGAGGACAATAGAGCGGAGCCCCCTGACCGGACTCTGGCC CCACCCCTTGCTGAACAGGGAGAAGGGAGGACTATAGAGCGGAGCCCCCTGACCGGACTCTGGCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1035663..1036460 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 110680 RMVar_ID_110680 Human_SNP_ID_803345941 m1A Human chr1 - 1623947 1623947 1623947 CGCCGCACAGGAGCCGGTGCGGCCCGGGACTCACGGGCGCGAGTGAGCGGTCTCGTAGCGGTCGA CGCCGCACAGGAGCCGGTGCGGCCCGGGACTCCCGGGCGCGAGTGAGCGGTCTCGTAGCGGTCGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1623901..1624151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable 7 stomach 110681 RMVar_ID_110681 Human_SNP_ID_803349989 m1A Human chr1 + 155014874 155014874 155014874 AGCTTTTCACTGAGGGCGGTGGCGGAGCTGTCATGGGGGCCGGGGGTAGCGGGACGGCCACTGGG AGCTTTTCACTGAGGGCGGTGGCGGAGCTGTCGTGGGGGCCGGGGGTAGCGGGACGGCCACTGGG A G ZBTB7B Ensembl:ENSG00000160685 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155014828..155015014 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_851784,Human_RBP_ID_3934093,Human_RBP_ID_3996980,Human_RBP_ID_5234364,Human_RBP_ID_5519192,Human_RBP_ID_22023862,Human_RBP_ID_27388855 110682 RMVar_ID_110682 Human_SNP_ID_803355641 m1A Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCGAAGGACCATTGCGTGGCCCACAAACTCTTTAA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10722 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,LAML,oesophagus adenocarcinoma,gastroesophageal_junction adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 oesophagus,stomach,haematopoietic and lymphoid tissue 110683 RMVar_ID_110683 Human_SNP_ID_803379271 m1A Human chr1 - 37482841 37482841 37482841 ATTTTTGTCCTTGCTTGGGGCTCTGGGGGGTGAGAGGAGAGCATTGGCACGGAGCTCATCTGCCA ATTTTTGTCCTTGCTTGGGGCTCTGGGGGGTGGGAGGAGAGCATTGGCACGGAGCTCATCTGCCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:37482829..37483069 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 110684 RMVar_ID_110684 Human_SNP_ID_803379733 m1A Human chr1 + 25901068 25901068 25901068 CAGCAGGGTCTTTGGATTCTTTGTTCTTCCGCACTTCTTCAATGTGCTTATCCTGTAAAGGAAGG CAGCAGGGTCTTTGGATTCTTTGTTCTTCCGCGCTTCTTCAATGTGCTTATCCTGTAAAGGAAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25900911..25901115 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 110685 RMVar_ID_110685 Human_SNP_ID_803384358 m1A Human chr1 + 203861676 203861676 203861676 TTTGTGAAATTCCACCATGGCGTACCGTGGCCAGGGTCAGAAAGTGCAGAAGGTTATGGTGCAGC TTTGTGAAATTCCACCATGGCGTACCGTGGCCGGGGTCAGAAAGTGCAGAAGGTTATGGTGCAGC A G SNRPE Ensembl:ENSG00000182004 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:203861626..203861725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_338430,Human_RBP_ID_744226,Human_RBP_ID_1419059,Human_RBP_ID_4074711,Human_RBP_ID_5311938,Human_RBP_ID_5741322,Human_RBP_ID_8961389,Human_RBP_ID_9319321,Human_RBP_ID_10732781,Human_RBP_ID_18560342,Human_RBP_ID_22431227,Human_RBP_ID_23205520,Human_RBP_ID_23356823 Human_Splice_Rec_176835,Human_Splice_Rec_176849,Human_Splice_Rec_176857 Human_miRNA_ID_2673970,Human_miRNA_ID_2924726 RMVar_hsa_circ_96625,RMVar_hsa_circ_139093 110686 RMVar_ID_110686 Human_SNP_ID_803385378 m1A Human chr1 - 154212368 154212368 154212368 CTCTTCCTTTCTCTTTCCTAAGGTCTTTGGCCAGAATGAGTACCTACGCTATCAGGAGGCCCTGA CTCTTCCTTTCTCTTTCCTAAGGTCTTTGGCCCGAATGAGTACCTACGCTATCAGGAGGCCCTGA T G C1orf43 Ensembl:ENSG00000143612 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154212301..154212400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_855280,Human_RBP_ID_5333708,Human_RBP_ID_8956342,Human_RBP_ID_19039236,Human_RBP_ID_22427530,Human_RBP_ID_26386446,Human_RBP_ID_26798923 Human_Splice_Rec_133786,Human_Splice_Rec_133787,Human_Splice_Rec_133798,Human_Splice_Rec_133799,Human_Splice_Rec_133812,Human_Splice_Rec_133813,Human_Splice_Rec_133820,Human_Splice_Rec_133821,Human_Splice_Rec_133830,Human_Splice_Rec_133831,Human_Splice_Rec_133850,Human_Splice_Rec_133851,Human_Splice_Rec_133856,Human_Splice_Rec_133857,Human_Splice_Rec_133868,Human_Splice_Rec_133876 RMVar_hsa_circ_136362,RMVar_hsa_circ_136359,RMVar_hsa_circ_121933,RMVar_hsa_circ_270644,RMVar_hsa_circ_314962,RMVar_hsa_circ_274629,RMVar_hsa_circ_136363,RMVar_hsa_circ_136361 110687 RMVar_ID_110687 Human_SNP_ID_803391521 m1A Human chr1 + 150629539 150629539 150629539 AAGGCAACCGGAGAAGGGAAGGGGGAGGGGAAACGGGGACAACCTGCGCTGCTGCTTCGGCTCCT AAGGCAACCGGAGAAGGGAAGGGGGAGGGGAATCGGGGACAACCTGCGCTGCTGCTTCGGCTCCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:150627526..150629600;chr1:150629362..150629625;chr1:150627501..150629625;chr1:150629349..150629625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 10 brain 110688 RMVar_ID_110688 Human_SNP_ID_803392459 m1A Human chr1 - 98661836 98661836 98661836 AGCACCTCCGCCTGCAGCAGGGCGGAAGAGCCACTGCTGCCCGGAAAGGGGGCGCCGCCCCCCGG AGCACCTCCGCCTGCAGCAGGGCGGAAGAGCCGCTGCTGCCCGGAAAGGGGGCGCCGCCCCCCGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:98661747..98661877 26863410 MeRIP-seq:(Medium) rs9728148 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma 11 head and neck 110689 RMVar_ID_110689 Human_SNP_ID_803401972 m1A Human chr1 + 181089450 181089450 181089450 GCGCCGCCCCTGCGGCTGCCCCCTAGGCGGGGAGGACCCGCCGGGTACACCGGCCGCGACCCCCC GCGCCGCCCCTGCGGCTGCCCCCTAGGCGGGGGGGACCCGCCGGGTACACCGGCCGCGACCCCCC A G IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:181089359..181089615 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_9270498 110690 RMVar_ID_110690 Human_SNP_ID_803429316 m1A Human chr1 - 70250505 70250505 70250505 CCAAATATAAAAATAAATCAATTTGTAAACATACTTTTACATCTTTATCACTCTCTGATTTTCTT CCAAATATAAAAATAAATCAATTTGTAAACATGCTTTTACATCTTTATCACTCTCTGATTTTCTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:70250476..70250525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 110691 RMVar_ID_110691 Human_SNP_ID_803449553 m1A Human chr1 - 150346428 150346428 150346428 CCACTTTATCCGATGCAGCATAAGACGCTTAAATTTCTTCTGGGCCTTGGGGCCTGGAAACAGAG CCACTTTATCCGATGCAGCATAAGACGCTTAACTTTCTTCTGGGCCTTGGGGCCTGGAAACAGAG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150346426..150346450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 110692 RMVar_ID_110692 Human_SNP_ID_803464204 m1A Human chr1 - 206696120 206696120 206696120 ACTTTTGTCCATGTCACTGATCTTTCTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAA ACTTTTGTCCATGTCACTGATCTTTCTGGCAAGGAAATCATCTGCCGTGTGACTGGTAGGATGAA T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:206696101..206696175 32194978 MeRIP-seq:(Medium) rs782188132 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue 110693 RMVar_ID_110693 Human_SNP_ID_803464296 m1A Human chr1 + 54715916 54715916 54715916 CGGGCTGGAAGGCAGGGCATCAGCTATGGAACAACCTGGGCAGGATCCCACCTCAGACGACGTCA CGGGCTGGAAGGCAGGGCATCAGCTATGGAACGACCTGGGCAGGATCCCACCTCAGACGACGTCA A G TTC4,MROH7-TTC4 Ensembl:ENSG00000243725,Ensembl:ENSG00000271723 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:54715866..54715992 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_1256672,Human_RBP_ID_1432819,Human_RBP_ID_1750742,Human_RBP_ID_4074082,Human_RBP_ID_5842599,Human_RBP_ID_8315010,Human_RBP_ID_11039459,Human_RBP_ID_17754571,Human_RBP_ID_26311326 RMVar_hsa_circ_133203,RMVar_hsa_circ_268827 110694 RMVar_ID_110694 Human_SNP_ID_803477494 m1A Human chr1 + 165827844 165827844 165827844 GGGAGGAGGGGCGGCGCGAACCATGGCCGGGGACAGCGAGCAGACCCTGCAGAACCACCAGCAGC GGGAGGAGGGGCGGCGCGAACCATGGCCGGGGGCAGCGAGCAGACCCTGCAGAACCACCAGCAGC A G UCK2 Ensembl:ENSG00000143179 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:165827626..165827952 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain Human_RBP_ID_25014,Human_RBP_ID_4005296,Human_RBP_ID_5705560,Human_RBP_ID_10631965 Human_Splice_Rec_153449,Human_Splice_Rec_153461 110695 RMVar_ID_110695 Human_SNP_ID_803490049 m1A Human chr1 + 1050561 1050561 1050561 GGCACTGCGGGACCGCCGCCTGGAGTTCCGCTACGACCTGGGCAAGGGGGCAGCGGTCATCAGGT GGCACTGCGGGACCGCCGCCTGGAGTTCCGCTGCGACCTGGGCAAGGGGGCAGCGGTCATCAGGT A G AGRN Ensembl:ENSG00000188157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1050426..1050617 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_223032,Human_RBP_ID_3932416,Human_RBP_ID_18966689,Human_RBP_ID_22557421,Human_RBP_ID_22750583 Human_Splice_Rec_1387,Human_Splice_Rec_1457,Human_Splice_Rec_1531,Human_Splice_Rec_1599 RMVar_hsa_circ_18675,RMVar_hsa_circ_35521,RMVar_hsa_circ_88386,RMVar_hsa_circ_128265,RMVar_hsa_circ_115507,RMVar_hsa_circ_128268,RMVar_hsa_circ_110165,RMVar_hsa_circ_128273,RMVar_hsa_circ_87140,RMVar_hsa_circ_110757,RMVar_hsa_circ_128275,RMVar_hsa_circ_128279 110696 RMVar_ID_110696 Human_SNP_ID_803494344 m1A Human chr1 - 156550348 156550348 156550348 CATCTTTTTTTTCTCCCTCAATCTGCCAGGTGACAGGGGATCCTGGAGCTGTGCTGTGGCTTGAG CATCTTTTTTTTCTCCCTCAATCTGCCAGGTGGCAGGGGATCCTGGAGCTGTGCTGTGGCTTGAG T C IQGAP3 Ensembl:ENSG00000183856 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156550301..156550350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18428725,Human_RBP_ID_22634483,Human_RBP_ID_24556570 Human_Splice_Rec_142974,Human_Splice_Rec_142975,Human_Splice_Rec_143044,Human_Splice_Rec_143045 RMVar_hsa_circ_5204,RMVar_hsa_circ_98213,RMVar_hsa_circ_136857,RMVar_hsa_circ_48002,RMVar_hsa_circ_63875,RMVar_hsa_circ_105275,RMVar_hsa_circ_98789,RMVar_hsa_circ_136863,RMVar_hsa_circ_80838,RMVar_hsa_circ_136864,RMVar_hsa_circ_136862,RMVar_hsa_circ_92144,RMVar_hsa_circ_110954,RMVar_hsa_circ_136866,RMVar_hsa_circ_128164,RMVar_hsa_circ_136867,RMVar_hsa_circ_38439,RMVar_hsa_circ_126915,RMVar_hsa_circ_84971,RMVar_hsa_circ_136869,RMVar_hsa_circ_111007,RMVar_hsa_circ_136870,RMVar_hsa_circ_136871,RMVar_hsa_circ_78813,RMVar_hsa_circ_360707,RMVar_hsa_circ_136872,RMVar_hsa_circ_120953,RMVar_hsa_circ_19393,RMVar_hsa_circ_136873,RMVar_hsa_circ_136874 110697 RMVar_ID_110697 Human_SNP_ID_803495542 m1A Human chr1 + 54225681 54225681 54225681 GGAGGGAGTAAAACAAAGACCAGCTACAGGGGAGGGAGGAAGGAGAAGGGCATGTCAATGTACAA GGAGGGAGTAAAACAAAGACCAGCTACAGGGGGGGGAGGAAGGAGAAGGGCATGTCAATGTACAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:54225630..54225958 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110698 RMVar_ID_110698 Human_SNP_ID_803521122 m1A Human chr1 + 988912 988912 988912 TTCAGGGTTGATTATTTCTGGTGTTCTGGGTTAATTGTTTCTGGAGTTCAGGGTTGATTGTTTCT TTCAGGGTTGATTATTTCTGGTGTTCTGGGTTGATTGTTTCTGGAGTTCAGGGTTGATTGTTTCT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:988894..989031 26863196 MeRIP-seq:(Medium) rs1181032059 Functional Loss SNV ICGC 33..33 33 COCA 1 - 110699 RMVar_ID_110699 Human_SNP_ID_803522467 m1A Human chr1 - 153670232 153670232 153670232 TTCAATGAGGTCAAAATAAAATCTGCATTTCTAGGGGTGACAGAGGCCGTGGTCGTGGTGGGCGC TTCAATGAGGTCAAAATAAAATCTGCATTTCTGGGGGTGACAGAGGCCGTGGTCGTGGTGGGCGC T C ILF2 Ensembl:ENSG00000143621 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:153670122..153670275;chr1:153670151..153670250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_326867,Human_RBP_ID_5691398,Human_RBP_ID_23206111 Human_Splice_Rec_131981,Human_Splice_Rec_132007,Human_Splice_Rec_132039,Human_Splice_Rec_132051 RMVar_hsa_circ_84560,RMVar_hsa_circ_136226,RMVar_hsa_circ_82146,RMVar_hsa_circ_136243 110700 RMVar_ID_110700 Human_SNP_ID_803522666 m1A Human chr1 - 75743072 75743072 75743072 CCTAGTGCTGGTATACTATAGAGAAACCCCCGAGGACCATGTGATTAAGTTCCTATCTTTTGAAA CCTAGTGCTGGTATACTATAGAGAAACCCCCGGGGACCATGTGATTAAGTTCCTATCTTTTGAAA T C - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs755963300 Functional Loss SNV ICGC 33..33 33 PBCA 2 - 110701 RMVar_ID_110701 Human_SNP_ID_803529097 m1A Human chr1 - 244862715 244862714 244862716 GCTCGTGTGTGTTTTAGGGGACGGCAAAACAGAACAGAAAGGCGGAGATAAAAAGAGGGGTGTTA GCTCGTGTGTGTTTTAGGGGACGGCAAAACA__ACAGAAAGGCGGAGATAAAAAGAGGGGTGTTA TTC T HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:244862704..244862788 26863410 MeRIP-seq:(Medium) rs770849021 Functional Loss DEL ICGC 32..33 33 LICA 1 - Human_RBP_ID_745159,Human_RBP_ID_4038806,Human_RBP_ID_5537587,Human_RBP_ID_10884133,Human_RBP_ID_17102550,Human_RBP_ID_22871669,Human_RBP_ID_23380421,Human_RBP_ID_24673718,Human_RBP_ID_26313008,Human_RBP_ID_26859435 Human_Splice_Rec_207222,Human_Splice_Rec_207223,Human_Splice_Rec_207274,Human_Splice_Rec_207275,Human_Splice_Rec_207312,Human_Splice_Rec_207313,Human_Splice_Rec_207334,Human_Splice_Rec_207335,Human_Splice_Rec_207355,Human_Splice_Rec_207408,Human_Splice_Rec_207409,Human_Splice_Rec_207478,Human_Splice_Rec_207479,Human_Splice_Rec_207512,Human_Splice_Rec_207513,Human_Splice_Rec_207548,Human_Splice_Rec_207549 RMVar_hsa_circ_71397,RMVar_hsa_circ_351017,RMVar_hsa_circ_53867,RMVar_hsa_circ_141264,RMVar_hsa_circ_68419,RMVar_hsa_circ_266514,RMVar_hsa_circ_55101,RMVar_hsa_circ_267436,RMVar_hsa_circ_48637,RMVar_hsa_circ_141276,RMVar_hsa_circ_295098 110702 RMVar_ID_110702 Human_SNP_ID_803531566 m1A Human chr1 + 202012690 202012690 202012690 CCCAGGAGCTGCTGGACGACGGTCAGCAAGCCAGCCCCTACCACCCCGGCAGCTGTGGCGCAGGA CCCAGGAGCTGCTGGACGACGGTCAGCAAGCCCGCCCCTACCACCCCGGCAGCTGTGGCGCAGGA A C AL691482.4,ELF3 Ensembl:ENSG00000249007,Ensembl:ENSG00000163435 lincRNA,Protein coding intron,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:202012642..202012774 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_5092341 Human_Splice_Rec_173560,Human_Splice_Rec_173561,Human_Splice_Rec_173576,Human_Splice_Rec_173577,Human_Splice_Rec_173592,Human_Splice_Rec_173593,Human_Splice_Rec_173608,Human_Splice_Rec_173609,Human_Splice_Rec_173622,Human_Splice_Rec_173623,Human_Splice_Rec_173627,Human_Splice_Rec_173631 RMVar_hsa_circ_138912,RMVar_hsa_circ_138911,RMVar_hsa_circ_373306,RMVar_hsa_circ_127473,RMVar_hsa_circ_364995 110703 RMVar_ID_110703 Human_SNP_ID_803534707 m1A Human chr1 - 26281168 26281168 26281168 AGGTCCTTCATGGCCAGGTGAAGGCTGGGGGGAGTGTGGTGATGGAGTCCAGCAGGGGAACTCTG AGGTCCTTCATGGCCAGGTGAAGGCTGGGGGGGGTGTGGTGATGGAGTCCAGCAGGGGAACTCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:26281119..26281318 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 110704 RMVar_ID_110704 Human_SNP_ID_803548845 m1A Human chr1 - 2391512 2391512 2391512 TCGGCGGCAAGATGGCAGCGGCGGGCGAGGGCACCCCGAGCTCCCGCGGGCCGCGTCGGGACCCG TCGGCGGCAAGATGGCAGCGGCGGGCGAGGGCCCCCCGAGCTCCCGCGGGCCGCGTCGGGACCCG T G MORN1 Ensembl:ENSG00000116151 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:2391455..2391527 26863196 MeRIP-seq:(Medium) rs986038009 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_223636 Human_Splice_Rec_7261,Human_Splice_Rec_7287,Human_Splice_Rec_7309,Human_Splice_Rec_7357 110705 RMVar_ID_110705 Human_SNP_ID_803550857 m1A Human chr1 - 952516 952516 952516 TCCCCTTCATCAGTTTCATGCAGTGGACCTTGACGGAGCTGCTGGCCCTGGAGCCGGGTGTGGCC TCCCCTTCATCAGTTTCATGCAGTGGACCTTGTCGGAGCTGCTGGCCCTGGAGCCGGGTGTGGCC T A NOC2L Ensembl:ENSG00000188976 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:952370..952527 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_23432,Human_RBP_ID_364562,Human_RBP_ID_3934748,Human_RBP_ID_4068358,Human_RBP_ID_5876074,Human_RBP_ID_8752583,Human_RBP_ID_9357776,Human_RBP_ID_11136031,Human_RBP_ID_18186692,Human_RBP_ID_23204878,Human_RBP_ID_26870943 Human_Splice_Rec_1070,Human_Splice_Rec_1110 Human_miRNA_ID_2571639,Human_miRNA_ID_2660716,Human_miRNA_ID_2679171 RMVar_hsa_circ_4241,RMVar_hsa_circ_118999,RMVar_hsa_circ_128238,RMVar_hsa_circ_113710,RMVar_hsa_circ_128239,RMVar_hsa_circ_128242,RMVar_hsa_circ_81243,RMVar_hsa_circ_104604,RMVar_hsa_circ_128243 110706 RMVar_ID_110706 Human_SNP_ID_803555566 m1A Human chr1 - 224015456 224015456 224015456 AGTCCATTCCATTGCATTCCATTCCATTCGAGACCATTCCATTGTATTCCATCCCAATCCTTTCG AGTCCATTCCATTGCATTCCATTCCATTCGAGTCCATTCCATTGTATTCCATCCCAATCCTTTCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:224015411..224015607 26863196 MeRIP-seq:(Medium) rs62652751 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110707 RMVar_ID_110707 Human_SNP_ID_803557626 m1A Human chr1 + 220046461 220046461 220046461 CGTGCCAGAACTACGGAGGACCCCGCGAAAGGAAGAAGATGCAACGTGTGCGCGTACCCGACGCC CGTGCCAGAACTACGGAGGACCCCGCGAAAGGCAGAAGATGCAACGTGTGCGCGTACCCGACGCC A C lnc-IARS2-2 RNACentral:URS00008C0502 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:220046351..220046572 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 110708 RMVar_ID_110708 Human_SNP_ID_803558219 m1A Human chr1 + 211341617 211341617 211341617 ATAAAGGACACAGGTCTGTGGGTGCCACCTGGAAGGTGTGTTTCCATCGGGCATTGCTCTGGAGC ATAAAGGACACAGGTCTGTGGGTGCCACCTGGGAGGTGTGTTTCCATCGGGCATTGCTCTGGAGC A G TRAF5 Ensembl:ENSG00000082512 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:211341615..211341698 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110709 RMVar_ID_110709 Human_SNP_ID_803569764 m1A Human chr1 - 109426367 109426367 109426367 TTGGGTGCCGGTGGAGTCGTGTTGGTCCTCAGAATCCCCGCGTAGCCGCTGCCTCCTCCTACCCT TTGGGTGCCGGTGGAGTCGTGTTGGTCCTCAGTATCCCCGCGTAGCCGCTGCCTCCTCCTACCCT T A PSMA5 Ensembl:ENSG00000143106 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109426108..109426377 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_25976,Human_RBP_ID_320300,Human_RBP_ID_858184,Human_RBP_ID_4074239,Human_RBP_ID_5311787,Human_RBP_ID_9270248,Human_RBP_ID_9319059,Human_RBP_ID_18546817,Human_RBP_ID_22427356,Human_RBP_ID_23205256,Human_RBP_ID_23321206,Human_RBP_ID_26836829,Human_RBP_ID_27385505 Human_Splice_Rec_105949,Human_Splice_Rec_105999 RMVar_hsa_circ_135214,RMVar_hsa_circ_121549 110710 RMVar_ID_110710 Human_SNP_ID_803571299 m1A Human chr1 + 206685302 206685302 206685302 TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCACCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG TCCCCGCCCCGGCCCCGCCGCCGCAGCCCCCCCCCCCTGCCCTGCCGCACCCCCCGGCGCAGCCG A C MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:206684876..206685493 26863410 MeRIP-seq:(Medium) rs181345810 Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_22532177 RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 110711 RMVar_ID_110711 Human_SNP_ID_803579311 m1A Human chr1 + 113653873 113653873 113653873 GAGGACGACAGCTCTCAGGCCTTCATTTCAACACAGAATGGATCTCCCCGCCTGAACCGGGCAGA GAGGACGACAGCTCTCAGGCCTTCATTTCAACGCAGAATGGATCTCCCCGCCTGAACCGGGCAGA A G MAGI3 Ensembl:ENSG00000081026 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2359173 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_17761 Human_Splice_Rec_111142,Human_Splice_Rec_111184,Human_Splice_Rec_111224,Human_Splice_Rec_111266 GWAS_ID_8442,GWAS_ID_8443,GWAS_ID_8444,GWAS_ID_8445,GWAS_ID_8446 RMVar_hsa_circ_4433,RMVar_hsa_circ_43524,RMVar_hsa_circ_65814,RMVar_hsa_circ_360372,RMVar_hsa_circ_55520,RMVar_hsa_circ_268019,RMVar_hsa_circ_69227,RMVar_hsa_circ_135455,RMVar_hsa_circ_59122,RMVar_hsa_circ_353328,RMVar_hsa_circ_373254,RMVar_hsa_circ_135456,RMVar_hsa_circ_316166,RMVar_hsa_circ_321292,RMVar_hsa_circ_135457,RMVar_hsa_circ_367407,RMVar_hsa_circ_61981,RMVar_hsa_circ_135460,RMVar_hsa_circ_29378,RMVar_hsa_circ_322177,RMVar_hsa_circ_287940,RMVar_hsa_circ_135462,RMVar_hsa_circ_135463,RMVar_hsa_circ_135461,RMVar_hsa_circ_357993,RMVar_hsa_circ_351711,RMVar_hsa_circ_135464,RMVar_hsa_circ_328130,RMVar_hsa_circ_284049 110712 RMVar_ID_110712 Human_SNP_ID_803580344 m1A Human chr1 + 3796004 3796004 3796004 GAAAGGAGTCTAGGCAATTGCCGGTGAGGTTGAGGCTCTGCAGGCGCGGGGCGCAGCGCGCCAGG GAAAGGAGTCTAGGCAATTGCCGGTGAGGTTGTGGCTCTGCAGGCGCGGGGCGCAGCGCGCCAGG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:3795953..3796083 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine 110713 RMVar_ID_110713 Human_SNP_ID_803595338 m1A Human chr1 - 45511279 45511279 45511279 TGCCAGGCTGCGGTGGGCAGCCATGAGAACAAAACCTCTTCTGTATTTTTTTTTTCCATTAGTAA TGCCAGGCTGCGGTGGGCAGCCATGAGAACAACACCTCTTCTGTATTTTTTTTTTCCATTAGTAA T G PRDX1 Ensembl:ENSG00000117450 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:45511228..45511342 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_356409,Human_RBP_ID_1256139,Human_RBP_ID_1348831,Human_RBP_ID_1748864,Human_RBP_ID_2149855,Human_RBP_ID_3314530,Human_RBP_ID_4096718,Human_RBP_ID_5830504,Human_RBP_ID_11005739,Human_RBP_ID_17218825,Human_RBP_ID_17336029,Human_RBP_ID_17453337,Human_RBP_ID_17646399,Human_RBP_ID_17752455,Human_RBP_ID_18576208,Human_RBP_ID_19154289,Human_RBP_ID_21878379,Human_RBP_ID_22427226,Human_RBP_ID_23398310,Human_RBP_ID_24397525,Human_RBP_ID_24455672,Human_RBP_ID_26391012,Human_RBP_ID_27184036 110714 RMVar_ID_110714 Human_SNP_ID_803603539 m1A Human chr1 - 148522708 148522708 148522708 CCACTATCACAAATTATGCAGTCGAGTTTCCCACATTTGGGGAAATCGCAGAGGTCAGCACATCT CCACTATCACAAATTATGCAGTCGAGTTTCCCTCATTTGGGGAAATCGCAGAGGTCAGCACATCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:148522659..148522736 26863196 MeRIP-seq:(Medium) rs1446871818 Functional Loss SNV ICGC 33..33 33 MALY 1 - 110715 RMVar_ID_110715 Human_SNP_ID_803605861 m1A Human chr1 + 227735185 227735163 227735185 AGGAGAAGGCGCCCGGCTCCGAGACGAAGGCTACCCGGCCCGGAGCCTGGCCGACGCCGGGGACA AGGAGAAGGCG______________________CCCGGCCCGGAGCCTGGCCGACGCCGGGGACA GCCCGGCTCCGAGACGAAGGCTA G SNAP47 Ensembl:ENSG00000143740 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:227735144..227735241 26863196 MeRIP-seq:(Medium) rs751658546 Functional Loss DEL ICGC 12..33 33 LICA 1 - RMVar_hsa_circ_99439,RMVar_hsa_circ_140207 110716 RMVar_ID_110716 Human_SNP_ID_803608599 m1A Human chr1 - 25229122 25229122 25229122 AGCTGACAGACTTCTTGTGTTACGGTTTTAGAATGAAGCTCGTAAATTAAATCACCAGGAAGTTG AGCTGACAGACTTCTTGTGTTACGGTTTTAGAGTGAAGCTCGTAAATTAAATCACCAGGAAGTTG T C SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25228944..25229176 26863196 MeRIP-seq:(Medium) rs764065825 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma,lung non_small_cell_carcinoma 6 lung Human_Splice_Rec_31970,Human_Splice_Rec_31990 RMVar_hsa_circ_52219,RMVar_hsa_circ_67009 110717 RMVar_ID_110717 Human_SNP_ID_803611200 m1A Human chr1 + 68232446 68232446 68232446 CTTCAGAGGTGCTGGAGCGCGGCGAGGATGGGACCGGGACGGAAGGCGCCCGCACGGATTCCCCC CTTCAGAGGTGCTGGAGCGCGGCGAGGATGGGGCCGGGACGGAAGGCGCCCGCACGGATTCCCCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:68232395..68232509 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 110718 RMVar_ID_110718 Human_SNP_ID_803629153 m1A Human chr1 - 230279355 230279355 230279355 CCCCGCTCTTGGCCGTGCGACTGTCCAGGCACAGGTTGCTGCCCACGTGCCTCAGCTTGGAGTTG CCCCGCTCTTGGCCGTGCGACTGTCCAGGCACGGGTTGCTGCCCACGTGCCTCAGCTTGGAGTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:230279275..230279413 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 110719 RMVar_ID_110719 Human_SNP_ID_803636392 m1A Human chr1 + 109421914 109421914 109421914 TCCACTTGAAATAATCTTCCTTCGGGAGAAAAAGTATTCACGCCCCTATAATTTAAAAAAAAATT TCCACTTGAAATAATCTTCCTTCGGGAGAAAACGTATTCACGCCCCTATAATTTAAAAAAAAATT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:109421851..109421950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110720 RMVar_ID_110720 Human_SNP_ID_803648655 m1A Human chr1 - 16960919 16960919 16960919 TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCAGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC TCGGCTGCGCTCAGCCGCAGGCCCAGCTCTGCGGCCTCGGCCCGCGCCGCCTCCAGCTTCAGCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16960870..16960971 26863196 MeRIP-seq:(Medium) rs2273113 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 2 head and neck GWAS_ID_7725,GWAS_ID_7726 110721 RMVar_ID_110721 Human_SNP_ID_803662486 m1A Human chr1 + 26827009 26827009 26827009 GGAGCGGGAGCCTCGGCCGCCGCCCACGGCGCAAGTGGGAGGTGTTCCCGGGTCGCAATCGCTTC GGAGCGGGAGCCTCGGCCGCCGCCCACGGCGCTAGTGGGAGGTGTTCCCGGGTCGCAATCGCTTC A T ZDHHC18 Ensembl:ENSG00000204160 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:26826958..26827059 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_350358,Human_RBP_ID_4093207 110722 RMVar_ID_110722 Human_SNP_ID_803674056 m1A Human chr1 + 85259608 85259608 85259608 AGCTGCTGCTCCCGTATGCCGCAAAATAGCTCAGAGGGTCCTTCTCCTCCGCTGCCATGACGGCT AGCTGCTGCTCCCGTATGCCGCAAAATAGCTCCGAGGGTCCTTCTCCTCCGCTGCCATGACGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:85259486..85259628 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 110723 RMVar_ID_110723 Human_SNP_ID_803678175 m1A Human chr1 - 53255150 53255150 53255150 CAAATGAAGACAGTAAGATGGGCTCAACAGTCACTGCCGCTGTTATCGGGATCATCGTGCCCATA CAAATGAAGACAGTAAGATGGGCTCAACAGTCGCTGCCGCTGTTATCGGGATCATCGTGCCCATA T C LRP8 Ensembl:ENSG00000157193 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:53255126..53255150 26863196 MeRIP-seq:(Medium) rs1162864808 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_RBP_ID_854756,Human_RBP_ID_26314261,Human_RBP_ID_26800569 Human_Splice_Rec_72178,Human_Splice_Rec_72179,Human_Splice_Rec_72212,Human_Splice_Rec_72213,Human_Splice_Rec_72218,Human_Splice_Rec_72219,Human_Splice_Rec_72246,Human_Splice_Rec_72247,Human_Splice_Rec_72274,Human_Splice_Rec_72275,Human_Splice_Rec_72310,Human_Splice_Rec_72311,Human_Splice_Rec_72342,Human_Splice_Rec_72343,Human_Splice_Rec_72374,Human_Splice_Rec_72375,Human_Splice_Rec_72408,Human_Splice_Rec_72409,Human_Splice_Rec_72416,Human_Splice_Rec_72417,Human_Splice_Rec_72450,Human_Splice_Rec_72451,Human_Splice_Rec_72482,Human_Splice_Rec_72483,Human_Splice_Rec_72506,Human_Splice_Rec_72507,Human_Splice_Rec_72536,Human_Splice_Rec_72537,Human_Splice_Rec_72569,Human_Splice_Rec_72576,Human_Splice_Rec_72577,Human_Splice_Rec_72614,Human_Splice_Rec_72615,Human_Splice_Rec_72650,Human_Splice_Rec_72651,Human_Splice_Rec_72680,Human_Splice_Rec_72681,Human_Splice_Rec_72710,Human_Splice_Rec_72711,Human_Splice_Rec_72740,Human_Splice_Rec_72741,Human_Splice_Rec_72774,Human_Splice_Rec_72775,Human_Splice_Rec_72800,Human_Splice_Rec_72801,Human_Splice_Rec_72808,Human_Splice_Rec_72809,Human_Splice_Rec_72840,Human_Splice_Rec_72841,Human_Splice_Rec_72876,Human_Splice_Rec_72877,Human_Splice_Rec_72894,Human_Splice_Rec_72895,Human_Splice_Rec_72926,Human_Splice_Rec_72927,Human_Splice_Rec_72940,Human_Splice_Rec_72952 RMVar_hsa_circ_10376,RMVar_hsa_circ_321133,RMVar_hsa_circ_47119,RMVar_hsa_circ_330103,RMVar_hsa_circ_377245,RMVar_hsa_circ_317086,RMVar_hsa_circ_133097,RMVar_hsa_circ_3041,RMVar_hsa_circ_360124,RMVar_hsa_circ_371160,RMVar_hsa_circ_133098 110724 RMVar_ID_110724 Human_SNP_ID_803686307 m1A Human chr1 + 65420739 65420739 65420739 GGCCCCAGTTCGGGAGACATGGCGGGCGTTAAAGGTACATCGCGGTCCCCGGCTCGCTTGTCGTG GGCCCCAGTTCGGGAGACATGGCGGGCGTTAATGGTACATCGCGGTCCCCGGCTCGCTTGTCGTG A T LEPROT,LEPR Ensembl:ENSG00000213625,Ensembl:ENSG00000116678 Protein coding,Protein coding CDS,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:65420717..65420792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 5 lung Human_RBP_ID_4074107,Human_RBP_ID_19034985,Human_RBP_ID_22871317 Human_Splice_Rec_82809,Human_Splice_Rec_82813,Human_Splice_Rec_82817,Human_Splice_Rec_82823,Human_Splice_Rec_82829,Human_Splice_Rec_82833,Human_Splice_Rec_82841,Human_Splice_Rec_82879,Human_Splice_Rec_82917 RMVar_hsa_circ_84010,RMVar_hsa_circ_133702 110725 RMVar_ID_110725 Human_SNP_ID_803698958 m1A Human chr1 + 109269183 109269183 109269183 CAGGAGCCAGAGGAGCTGGCACGGCGACAGCGACGGCACCCGGAGCTGAGCCAGGGTGAGGCTGT CAGGAGCCAGAGGAGCTGGCACGGCGACAGCGTCGGCACCCGGAGCTGAGCCAGGGTGAGGCTGT A T CELSR2 Ensembl:ENSG00000143126 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109269133..109269234 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_17763895 Human_Splice_Rec_105628 Human_miRNA_ID_2082136,Human_miRNA_ID_2268196 RMVar_hsa_circ_28435,RMVar_hsa_circ_127397,RMVar_hsa_circ_80736,RMVar_hsa_circ_124530,RMVar_hsa_circ_135155,RMVar_hsa_circ_135157,RMVar_hsa_circ_91089,RMVar_hsa_circ_94158,RMVar_hsa_circ_135158,RMVar_hsa_circ_135159,RMVar_hsa_circ_103760,RMVar_hsa_circ_135160,RMVar_hsa_circ_135161,RMVar_hsa_circ_116694,RMVar_hsa_circ_135163,RMVar_hsa_circ_89540,RMVar_hsa_circ_135164,RMVar_hsa_circ_94875,RMVar_hsa_circ_135165 110726 RMVar_ID_110726 Human_SNP_ID_803707353 m1A Human chr1 - 1043876 1043874 1043876 GGGCGGGGGGTGCTCACACCGGGGACACACACACTGCCCTGCGGAGCACACAGCCCCAAAAGCAC GGGCGGGGGGTGCTCACACCGGGGACACACAC__TGCCCTGCGGAGCACACAGCCCCAAAAGCAC AGT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1043826..1044000 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..34 33 COAD,STAD 3 - 110727 RMVar_ID_110727 Human_SNP_ID_803717629 m1A Human chr1 - 153986303 153986303 153986303 CTGGCCTGGGCTCCGTGCCGCTCTGTTTGCCAACCGTCCAGTCCCGCCTACCAGTGCCGGGCGCT CTGGCCTGGGCTCCGTGCCGCTCTGTTTGCCACCCGTCCAGTCCCGCCTACCAGTGCCGGGCGCT T G RAB13 Ensembl:ENSG00000143545 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:153986266..153986348 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_4073041,Human_RBP_ID_26801028 Human_miRNA_ID_137703,Human_miRNA_ID_423192,Human_miRNA_ID_1146973,Human_miRNA_ID_1149695,Human_miRNA_ID_1151005,Human_miRNA_ID_1152402,Human_miRNA_ID_1153680,Human_miRNA_ID_1154988,Human_miRNA_ID_1160221,Human_miRNA_ID_1161551,Human_miRNA_ID_2131064 RMVar_hsa_circ_136344,RMVar_hsa_circ_124620,RMVar_hsa_circ_136346,RMVar_hsa_circ_76770 110728 RMVar_ID_110728 Human_SNP_ID_803718407 m1A Human chr1 - 43530923 43530923 43530923 CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGAAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG CGGAGCCGGAGCCCGAGCCCGAGCCGGAGCCGGAGCTGGAGCCGCCGCCTCTGCCGCCGCCACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:43530876..43538315;chr1:43530842..43531123;chr1:43530826..43545125;chr1:43530876..43545068 26863196 MeRIP-seq:(Medium) rs1239474344 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast 110729 RMVar_ID_110729 Human_SNP_ID_803718539 m1A Human chr1 - 51840366 51840365 51840366 AAGAAGATGATGATGAAGATTCTGGAGCTGAAATAGAAGATGACGATGAAGAGGGTTTTGATGAT AAGAAGATGATGATGAAGATTCTGGAGCTGAA_TAGAAGATGACGATGAAGAGGGTTTTGATGAT AT A NRDC Ensembl:ENSG00000078618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51840276..51840475 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_854732,Human_RBP_ID_1438147,Human_RBP_ID_1750070,Human_RBP_ID_5537949,Human_RBP_ID_5838054,Human_RBP_ID_18410167,Human_RBP_ID_22735128,Human_RBP_ID_22865660,Human_RBP_ID_23112542,Human_RBP_ID_23117553,Human_RBP_ID_23401270,Human_RBP_ID_24541120,Human_RBP_ID_26311273,Human_RBP_ID_27798036 RMVar_hsa_circ_11979,RMVar_hsa_circ_132887,RMVar_hsa_circ_356702,RMVar_hsa_circ_62314,RMVar_hsa_circ_62713,RMVar_hsa_circ_60868,RMVar_hsa_circ_359022,RMVar_hsa_circ_121225,RMVar_hsa_circ_354092,RMVar_hsa_circ_307241,RMVar_hsa_circ_132912,RMVar_hsa_circ_132913,RMVar_hsa_circ_132914,RMVar_hsa_circ_355831,RMVar_hsa_circ_350303 110730 RMVar_ID_110730 Human_SNP_ID_803726471 m1A Human chr1 + 1108156 1108156 1108156 ACAGCCACCATGTCTCAGCAGCACCGTCCACCACAGCCACCATGTCTCAGCACCGTTCACCACAG ACAGCCACCATGTCTCAGCAGCACCGTCCACCGCAGCCACCATGTCTCAGCACCGTTCACCACAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1108107..1108216 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 110731 RMVar_ID_110731 Human_SNP_ID_803781061 m1A Human chr1 - 51878697 51878697 51878697 TCAGGCCTGTTCCCCGCGGCTGCGGCAGCACCAGGGCCGGCCGCCACCGCCTCTAGAACGCGGAG TCAGGCCTGTTCCCCGCGGCTGCGGCAGCACCGGGGCCGGCCGCCACCGCCTCTAGAACGCGGAG T C NRDC Ensembl:ENSG00000078618 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:51878326..51878775 26863196 MeRIP-seq:(Medium) rs971483887 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17711,Human_RBP_ID_741646,Human_RBP_ID_858817,Human_RBP_ID_4058275,Human_RBP_ID_5519004,Human_RBP_ID_9270148,Human_RBP_ID_18414962,Human_RBP_ID_18468577,Human_RBP_ID_22023374,Human_RBP_ID_26311280,Human_RBP_ID_26866394,Human_RBP_ID_27798039 RMVar_hsa_circ_121225,RMVar_hsa_circ_132913 110732 RMVar_ID_110732 Human_SNP_ID_803783742 m1A Human chr1 + 116395108 116395108 116395108 CTGAAATTTTCAAAGGCTCCTGTCCTCCTCGCAGGTTTCTGCCACCTCTTTCTGCCAGATGAACA CTGAAATTTTCAAAGGCTCCTGTCCTCCTCGCTGGTTTCTGCCACCTCTTTCTGCCAGATGAACA A T ATP1A1 Ensembl:ENSG00000163399 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:116395101..116395125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung RMVar_hsa_circ_12349,RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_78811,RMVar_hsa_circ_135609,RMVar_hsa_circ_135612,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_64344,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_135618,RMVar_hsa_circ_135619,RMVar_hsa_circ_112954,RMVar_hsa_circ_69417,RMVar_hsa_circ_5028,RMVar_hsa_circ_135621,RMVar_hsa_circ_109389,RMVar_hsa_circ_79272,RMVar_hsa_circ_135622 110733 RMVar_ID_110733 Human_SNP_ID_803824259 m1A Human chr1 - 1471992 1471992 1471992 CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAAACCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG CATTTGTCCTTGGGCGCCGGCCGGTCTCCCAAGCCGCGGTCCCCGCCGCCCTCGGCCCCGGGCTG T C lnc-TMEM240-2 RNACentral:URS0000D5CEEB lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1471794..1472050 26863196 MeRIP-seq:(Medium) rs188574574 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 5 head and neck 110734 RMVar_ID_110734 Human_SNP_ID_803827434 m1A Human chr1 - 16621161 16621161 16621161 AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCATGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG AAGCTCTTTCCGAAAGTGCTGGGATTCCAGGCGTGAGCTATGGTGAAGCTCTTAAAGAAGGGGTG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs11260839 Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_5711081,Human_RBP_ID_8051634,Human_RBP_ID_8242521,Human_RBP_ID_9410452,Human_RBP_ID_18930564,Human_RBP_ID_21963551 RMVar_hsa_circ_56321 110735 RMVar_ID_110735 Human_SNP_ID_803837326 m1A Human chr1 - 234373612 234373612 234373612 GTCGACGGGAGGAAACTGTCACGCAGGCCACCAACCGGCGGTGGAGGGCGCGGTGCCGAGTCCTG GTCGACGGGAGGAAACTGTCACGCAGGCCACCCACCGGCGGTGGAGGGCGCGGTGCCGAGTCCTG T G COA6-AS1,COA6-AS1:2,COA6-AS1:3,COA6-AS1:4 RNACentral:URS0000D57BF2,RNACentral:URS0000D5A78E,RNACentral:URS0000D5CAC3,RNACentral:URS0000D5DD6B lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:234373503..234373750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110736 RMVar_ID_110736 Human_SNP_ID_803841192 m1A Human chr1 + 149886407 149886407 149886407 GTGGAGCGCTTGTTGTAGTGCGCCAGGCGGGAAGCCTCTCCCGCGATGCGCTCGAAGATGTCGTT GTGGAGCGCTTGTTGTAGTGCGCCAGGCGGGAGGCCTCTCCCGCGATGCGCTCGAAGATGTCGTT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:149886309..149886675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 110737 RMVar_ID_110737 Human_SNP_ID_803841310 m1A Human chr1 + 63962589 63962589 63962589 AGAAAAGCCTCCCTGGAGTTGGTGATGATTTAACTGCATCTCAAATAATGATCAGACATCCATCA AGAAAAGCCTCCCTGGAGTTGGTGATGATTTAGCTGCATCTCAAATAATGATCAGACATCCATCA A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:63962583..63962876 26863196 MeRIP-seq:(Medium) rs1048044400 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110738 RMVar_ID_110738 Human_SNP_ID_803857610 m1A Human chr1 - 1320531 1320531 1320531 ACTGTGCAACCTGAAACCCCCACATCCTTCCTAGCGACGCTTCCCTGACTTCTCCTACATCACCC ACTGTGCAACCTGAAACCCCCACATCCTTCCTTGCGACGCTTCCCTGACTTCTCCTACATCACCC T A INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr1:1320451..1320603;chr1:1320451..1320700;chr1:1320455..1320755 26863410,26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin Merkel_cell_carcinoma 10 skin Human_RBP_ID_19040654,Human_RBP_ID_22786763 Human_Splice_Rec_2825,Human_Splice_Rec_2859,Human_Splice_Rec_2917,Human_Splice_Rec_2937,Human_Splice_Rec_2969,Human_Splice_Rec_3091,Human_Splice_Rec_3175,Human_Splice_Rec_3209,Human_Splice_Rec_3267,Human_Splice_Rec_3341,Human_Splice_Rec_3361,Human_Splice_Rec_3373,Human_Splice_Rec_3397,Human_Splice_Rec_3411,Human_Splice_Rec_3425,Human_Splice_Rec_3439,Human_Splice_Rec_3447,Human_Splice_Rec_3451,Human_Splice_Rec_3459,Human_Splice_Rec_3465,Human_Splice_Rec_3471,Human_Splice_Rec_3477,Human_Splice_Rec_3483,Human_Splice_Rec_3493,Human_Splice_Rec_3499 RMVar_hsa_circ_25202,RMVar_hsa_circ_55849,RMVar_hsa_circ_332407 110739 RMVar_ID_110739 Human_SNP_ID_803859814 m1A Human chr1 + 54728354 54728354 54728354 GATGCATCTAAATTTCATTTTTAGCGAATTGAACAGAGGGATGTGAGGAAAGCCAACTTGAAAGA GATGCATCTAAATTTCATTTTTAGCGAATTGAGCAGAGGGATGTGAGGAAAGCCAACTTGAAAGA A G TTC4,MROH7-TTC4 Ensembl:ENSG00000243725,Ensembl:ENSG00000271723 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:54722715..54728370 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_26314270,Human_RBP_ID_27185018,Human_RBP_ID_27798091 Human_Splice_Rec_74634,Human_Splice_Rec_74635,Human_Splice_Rec_74700,Human_Splice_Rec_74701,Human_Splice_Rec_74764,Human_Splice_Rec_74765,Human_Splice_Rec_74796,Human_Splice_Rec_74797,Human_Splice_Rec_74814,Human_Splice_Rec_74815,Human_Splice_Rec_74834,Human_Splice_Rec_74835 RMVar_hsa_circ_268827,RMVar_hsa_circ_57812,RMVar_hsa_circ_351382,RMVar_hsa_circ_348470,RMVar_hsa_circ_96740,RMVar_hsa_circ_347901,RMVar_hsa_circ_133207 110740 RMVar_ID_110740 Human_SNP_ID_803860000 m1A Human chr1 - 37692607 37692607 37692607 AAACTGGGTAGGGACGAGGAGGGCGGACGGGGACCACCCGAAGAAGTCGCCAGGCACGTACCTGC AAACTGGGTAGGGACGAGGAGGGCGGACGGGGGCCACCCGAAGAAGTCGCCAGGCACGTACCTGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:37692568..37692745 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110741 RMVar_ID_110741 Human_SNP_ID_803875440 m1A Human chr1 + 228256809 228256803 228256809 GGAAGAAGCTGAGCTTCAGCTCGAAAGTGCGCATGGAGGCTGTGGGCTGCACACGGAGGCTGGTG GGAAGAAGCTGAGCTTCAGCTCGAAAG______TGGAGGCTGTGGGCTGCACACGGAGGCTGGTG GTGCGCA G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:228256761..228256928 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 28..33 33 LIHC 2 - RMVar_hsa_circ_32576,RMVar_hsa_circ_10774,RMVar_hsa_circ_68043,RMVar_hsa_circ_363380,RMVar_hsa_circ_75212,RMVar_hsa_circ_67854,RMVar_hsa_circ_31451,RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_64814,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225 110742 RMVar_ID_110742 Human_SNP_ID_803877045 m1A Human chr1 - 228219464 228219464 228219464 GCCCACAGCCTCCACGTGCACTTTCGAGCTGGAGCTCAACTTCTTCCCGTCCTTGTACCACGTCA GCCCACAGCCTCCACGTGCACTTTCGAGCTGGTGCTCAACTTCTTCCCGTCCTTGTACCACGTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228219355..228219536 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110743 RMVar_ID_110743 Human_SNP_ID_803895110 m1A Human chr1 + 107505306 107505306 107505306 TGGAGCTTCTGGAGCAACACTGTATCTCTTGCATCTGGCATTGTTCAATCCAGATGTTTGTTGGG TGGAGCTTCTGGAGCAACACTGTATCTCTTGCGTCTGGCATTGTTCAATCCAGATGTTTGTTGGG A G AC114491.1 Ensembl:ENSG00000224550 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs529972278 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_22778750,Human_RBP_ID_26389489,Human_RBP_ID_26836494 110744 RMVar_ID_110744 Human_SNP_ID_803896441 m1A Human chr1 - 156595295 156595295 156595295 CAGCCGAAGAAAGAAGAGGCAGCAACAGGAGGAGGAGGACTTGAACCTAGAAGATAGAGGTGAGG CAGCCGAAGAAAGAAGAGGCAGCAACAGGAGGCGGAGGACTTGAACCTAGAAGATAGAGGTGAGG T G GPATCH4 Ensembl:ENSG00000160818 Protein coding CDS GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_2180709,Human_RBP_ID_5697331,Human_RBP_ID_22486119 110745 RMVar_ID_110745 Human_SNP_ID_803898124 m1A Human chr1 - 224114205 224114205 224114205 GGGCGGTGGAGGCTGTCGCTGGGTAGAGCCGGAGGCCAAAGAGGAACCGCCGTCGCCTTGGCCGC GGGCGGTGGAGGCTGTCGCTGGGTAGAGCCGGCGGCCAAAGAGGAACCGCCGTCGCCTTGGCCGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:224114154..224114288 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 110746 RMVar_ID_110746 Human_SNP_ID_803914175 m1A Human chr1 - 19383769 19383769 19383769 AGGAGCAGGCATAGGGACACTTTAAGCTTGAGAGGCCCATTAGATCAAAGTGGAGATACCAGGTA AGGAGCAGGCATAGGGACACTTTAAGCTTGAGTGGCCCATTAGATCAAAGTGGAGATACCAGGTA T A CAPZB Ensembl:ENSG00000077549 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:19383764..19383938 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_5926,RMVar_hsa_circ_61484,RMVar_hsa_circ_72794,RMVar_hsa_circ_330593,RMVar_hsa_circ_91800,RMVar_hsa_circ_275937,RMVar_hsa_circ_129828,RMVar_hsa_circ_310208,RMVar_hsa_circ_129829 110747 RMVar_ID_110747 Human_SNP_ID_803956175 m1A Human chr1 + 65395004 65395004 65395004 TCCAGTGCTTCCAGTGACCCCTTTCTCCAGCCAACAAGAAGTCCTTCGCCCACAGTACATGGTAA TCCAGTGCTTCCAGTGACCCCTTTCTCCAGCCCACAAGAAGTCCTTCGCCCACAGTACATGGTAA A C DNAJC6 Ensembl:ENSG00000116675 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4582839 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_3933625,Human_RBP_ID_22559424 Human_Splice_Rec_82711,Human_Splice_Rec_82747,Human_Splice_Rec_82787 GWAS_ID_8128,GWAS_ID_8129,GWAS_ID_8130,GWAS_ID_8131 RMVar_hsa_circ_314738,RMVar_hsa_circ_348663,RMVar_hsa_circ_319680,RMVar_hsa_circ_314537,RMVar_hsa_circ_117635,RMVar_hsa_circ_133691,RMVar_hsa_circ_133692,RMVar_hsa_circ_133690,RMVar_hsa_circ_43617,RMVar_hsa_circ_343019,RMVar_hsa_circ_29406,RMVar_hsa_circ_42839 110748 RMVar_ID_110748 Human_SNP_ID_803974651 m1A Human chr1 + 121374827 121374827 121374827 AGGTAAAAGTGAACTTCTGTTTCCTTTTCAGCACCAAGCCAAGTACACGGAGAATAAGCTGAAGG AGGTAAAAGTGAACTTCTGTTTCCTTTTCAGCGCCAAGCCAAGTACACGGAGAATAAGCTGAAGG A G SRGAP2C Ensembl:ENSG00000171943 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs61806690 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 38 head and neck Human_RBP_ID_18158548,Human_RBP_ID_18523707,Human_RBP_ID_27800681 Human_Splice_Rec_116716,Human_Splice_Rec_116730 Human_miRNA_ID_1861242,Human_miRNA_ID_2464533,Human_miRNA_ID_2464534 RMVar_hsa_circ_297478,RMVar_hsa_circ_308833,RMVar_hsa_circ_9042,RMVar_hsa_circ_287284,RMVar_hsa_circ_135771 110749 RMVar_ID_110749 Human_SNP_ID_803985479 m1A Human chr1 - 212445930 212445930 212445930 TGAAGTCCAGGTTAGGGCTGCCATCCTCATTGAGAATTCTCCGGGCAGTGTAGCCGACGATGGGG TGAAGTCCAGGTTAGGGCTGCCATCCTCATTGTGAATTCTCCGGGCAGTGTAGCCGACGATGGGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:212445880..212446062 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney 110750 RMVar_ID_110750 Human_SNP_ID_803991097 m1A Human chr1 + 201829297 201829297 201829297 AAGGATTAAAGGAAGCGTTAGTGGATACGCTCACCGGGATCCTATCCCCAGTACAGGAGGTGCGG AAGGATTAAAGGAAGCGTTAGTGGATACGCTCGCCGGGATCCTATCCCCAGTACAGGAGGTGCGG A G IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:201829203..201829412;chr1:201829201..201829363 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_272207,Human_RBP_ID_337606,Human_RBP_ID_4077119,Human_RBP_ID_9271695,Human_RBP_ID_9357380,Human_RBP_ID_18559786,Human_RBP_ID_18966302,Human_RBP_ID_22871877,Human_RBP_ID_26309875,Human_RBP_ID_27799083 Human_Splice_Rec_173275,Human_Splice_Rec_173285 RMVar_hsa_circ_84187,RMVar_hsa_circ_138839 110751 RMVar_ID_110751 Human_SNP_ID_803995245 m1A Human chr1 - 114720647 114720646 114720647 GGGATGGCCAACAAAGGGGATTGCCTGCAGAAAGGGGAGAGCGTCAAGTTCCAATTGTGTGTCCT GGGATGGCCAACAAAGGGGATTGCCTGCAGAA_GGGGAGAGCGTCAAGTTCCAATTGTGTGTCCT CT C CSDE1 Ensembl:ENSG00000009307 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:114720505..114720712 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_220963,Human_RBP_ID_322399,Human_RBP_ID_741294,Human_RBP_ID_800870,Human_RBP_ID_858280,Human_RBP_ID_1723015,Human_RBP_ID_5675990,Human_RBP_ID_8281918,Human_RBP_ID_8733149,Human_RBP_ID_8954397,Human_RBP_ID_9252960,Human_RBP_ID_17211517,Human_RBP_ID_17763970,Human_RBP_ID_22373168,Human_RBP_ID_22430795,Human_RBP_ID_22779201,Human_RBP_ID_23325250,Human_RBP_ID_26800811,Human_RBP_ID_26838350 Human_Splice_Rec_112860,Human_Splice_Rec_112898,Human_Splice_Rec_112934,Human_Splice_Rec_112970,Human_Splice_Rec_113002,Human_Splice_Rec_113034,Human_Splice_Rec_113070,Human_Splice_Rec_113106,Human_Splice_Rec_113118,Human_Splice_Rec_113120 RMVar_hsa_circ_1908,RMVar_hsa_circ_114327,RMVar_hsa_circ_307152,RMVar_hsa_circ_135556,RMVar_hsa_circ_316681,RMVar_hsa_circ_352189,RMVar_hsa_circ_340809,RMVar_hsa_circ_307470,RMVar_hsa_circ_276222,RMVar_hsa_circ_278572,RMVar_hsa_circ_19221,RMVar_hsa_circ_18439,RMVar_hsa_circ_135558,RMVar_hsa_circ_135560,RMVar_hsa_circ_135561,RMVar_hsa_circ_135562,RMVar_hsa_circ_135559,RMVar_hsa_circ_58281,RMVar_hsa_circ_372518,RMVar_hsa_circ_135563,RMVar_hsa_circ_92351,RMVar_hsa_circ_57169,RMVar_hsa_circ_135564,RMVar_hsa_circ_135565 110752 RMVar_ID_110752 Human_SNP_ID_804016885 m1A Human chr1 + 171535381 171535381 171535381 ACCTCAGTCTTTGTAAAAATCCTGTGTTTGATAAGTGTCATAGATGAATACTATTACCTTTCACC ACCTCAGTCTTTGTAAAAATCCTGTGTTTGATGAGTGTCATAGATGAATACTATTACCTTTCACC A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:171535378..171535542 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1729098,Human_RBP_ID_17589631,Human_RBP_ID_22634627 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_62597,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137527,RMVar_hsa_circ_93871,RMVar_hsa_circ_96232,RMVar_hsa_circ_137528,RMVar_hsa_circ_2974,RMVar_hsa_circ_24339,RMVar_hsa_circ_273818,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_137540,RMVar_hsa_circ_97212,RMVar_hsa_circ_137544,RMVar_hsa_circ_57086,RMVar_hsa_circ_84063,RMVar_hsa_circ_137545,RMVar_hsa_circ_137543 110753 RMVar_ID_110753 Human_SNP_ID_804017638 m1A Human chr1 + 43360783 43360783 43360783 CATCCACCACCATGATGTTCGGGTAGCAGAACACCATGTGGCCACACTGAGTGGCCACAGCCAGG CATCCACCACCATGATGTTCGGGTAGCAGAACTCCATGTGGCCACACTGAGTGGCCACAGCCAGG A T CDC20 Ensembl:ENSG00000117399 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43360726..43360800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_978465,Human_RBP_ID_9268798,Human_RBP_ID_22429324,Human_RBP_ID_22488228,Human_RBP_ID_22633559,Human_RBP_ID_27399033 Human_Splice_Rec_57508,Human_Splice_Rec_57526,Human_Splice_Rec_57538 Human_miRNA_ID_2673805,Human_miRNA_ID_2924562 RMVar_hsa_circ_106802,RMVar_hsa_circ_82216,RMVar_hsa_circ_125335,RMVar_hsa_circ_132236,RMVar_hsa_circ_132237,RMVar_hsa_circ_127354,RMVar_hsa_circ_132241,RMVar_hsa_circ_2646,RMVar_hsa_circ_116176,RMVar_hsa_circ_132242,RMVar_hsa_circ_132243 110754 RMVar_ID_110754 Human_SNP_ID_804020428 m1A Human chr1 + 7777252 7777252 7777252 GAGTTAGACGACCGTGCAGACGCACTGCAGGCAGGCGCTTCTCAATTTGAAACGAGCGCAGCCAA GAGTTAGACGACCGTGCAGACGCACTGCAGGCGGGCGCTTCTCAATTTGAAACGAGCGCAGCCAA A G VAMP3 Ensembl:ENSG00000049245 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:7777205..7778153 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_5866512,Human_RBP_ID_8975275,Human_RBP_ID_17337929 Human_Splice_Rec_13440,Human_Splice_Rec_13441,Human_Splice_Rec_13448,Human_Splice_Rec_13449,Human_Splice_Rec_13453 RMVar_hsa_circ_128694,RMVar_hsa_circ_99187,RMVar_hsa_circ_98071,RMVar_hsa_circ_128695,RMVar_hsa_circ_75740,RMVar_hsa_circ_128696,RMVar_hsa_circ_106270,RMVar_hsa_circ_311681,RMVar_hsa_circ_270541,RMVar_hsa_circ_128697,RMVar_hsa_circ_128698 110755 RMVar_ID_110755 Human_SNP_ID_804033084 m1A Human chr1 + 150578476 150578476 150578476 ACGATTTCACATCGTCTTCGTTTTTGATGTCCAGTTTCCGAAGCATGCCTGAGAAAGAAAAGCAT ACGATTTCACATCGTCTTCGTTTTTGATGTCCTGTTTCCGAAGCATGCCTGAGAAAGAAAAGCAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:150578426..150578500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 110756 RMVar_ID_110756 Human_SNP_ID_804038844 m1A Human chr1 + 220786945 220786945 220786945 CTTGCCGCCGCCACCTCGCGGAGAAGCCAGCCATGGGCGCCGCCGGCTCCTCCGCGCTGGCGCGC CTTGCCGCCGCCACCTCGCGGAGAAGCCAGCCTTGGGCGCCGCCGGCTCCTCCGCGCTGGCGCGC A T MTARC1 Ensembl:ENSG00000186205 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:220786901..220787125 26863196 MeRIP-seq:(Medium) rs905438821 Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 1 pancreas Human_RBP_ID_4025574,Human_RBP_ID_8298891 110757 RMVar_ID_110757 Human_SNP_ID_804041959 m1A Human chr1 - 21872762 21872762 21872762 TCCCCTGCCTGCCTCCTTCCATCCGTCTACCCAGGCCCAGGTGGAAGGCCTCACTTGCAGCCACT TCCCCTGCCTGCCTCCTTCCATCCGTCTACCCGGGCCCAGGTGGAAGGCCTCACTTGCAGCCACT T C HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:21872751..21872775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_77542,RMVar_hsa_circ_130113,RMVar_hsa_circ_86448,RMVar_hsa_circ_102515,RMVar_hsa_circ_110093,RMVar_hsa_circ_130115,RMVar_hsa_circ_130114,RMVar_hsa_circ_103955,RMVar_hsa_circ_130120,RMVar_hsa_circ_107661,RMVar_hsa_circ_115799,RMVar_hsa_circ_126118,RMVar_hsa_circ_130137,RMVar_hsa_circ_83177,RMVar_hsa_circ_79396,RMVar_hsa_circ_88294,RMVar_hsa_circ_107184,RMVar_hsa_circ_130141,RMVar_hsa_circ_130142,RMVar_hsa_circ_130139,RMVar_hsa_circ_130140,RMVar_hsa_circ_130138,RMVar_hsa_circ_104481,RMVar_hsa_circ_130150,RMVar_hsa_circ_127734,RMVar_hsa_circ_109194,RMVar_hsa_circ_96196,RMVar_hsa_circ_98813,RMVar_hsa_circ_98645,RMVar_hsa_circ_92297,RMVar_hsa_circ_91062,RMVar_hsa_circ_130163,RMVar_hsa_circ_85440,RMVar_hsa_circ_130165,RMVar_hsa_circ_130166,RMVar_hsa_circ_130164,RMVar_hsa_circ_130159,RMVar_hsa_circ_130161,RMVar_hsa_circ_130162,RMVar_hsa_circ_130160,RMVar_hsa_circ_130157,RMVar_hsa_circ_130158,RMVar_hsa_circ_106262,RMVar_hsa_circ_123609,RMVar_hsa_circ_114030,RMVar_hsa_circ_97779,RMVar_hsa_circ_92999,RMVar_hsa_circ_130185,RMVar_hsa_circ_130183,RMVar_hsa_circ_130184,RMVar_hsa_circ_130182,RMVar_hsa_circ_113529,RMVar_hsa_circ_103641,RMVar_hsa_circ_88033,RMVar_hsa_circ_91121,RMVar_hsa_circ_79093,RMVar_hsa_circ_130202,RMVar_hsa_circ_130206,RMVar_hsa_circ_130204,RMVar_hsa_circ_130205,RMVar_hsa_circ_130203,RMVar_hsa_circ_114680,RMVar_hsa_circ_130201,RMVar_hsa_circ_130221,RMVar_hsa_circ_118438,RMVar_hsa_circ_130223,RMVar_hsa_circ_102644,RMVar_hsa_circ_130224,RMVar_hsa_circ_119604,RMVar_hsa_circ_130231,RMVar_hsa_circ_123757,RMVar_hsa_circ_130232,RMVar_hsa_circ_85332,RMVar_hsa_circ_85524,RMVar_hsa_circ_130247,RMVar_hsa_circ_7703,RMVar_hsa_circ_87462,RMVar_hsa_circ_106371,RMVar_hsa_circ_130261,RMVar_hsa_circ_130262,RMVar_hsa_circ_109266,RMVar_hsa_circ_130273,RMVar_hsa_circ_130283,RMVar_hsa_circ_108100,RMVar_hsa_circ_99848,RMVar_hsa_circ_77075,RMVar_hsa_circ_130286,RMVar_hsa_circ_100811,RMVar_hsa_circ_130289,RMVar_hsa_circ_112020,RMVar_hsa_circ_130290,RMVar_hsa_circ_14998,RMVar_hsa_circ_104450,RMVar_hsa_circ_130291,RMVar_hsa_circ_130292,RMVar_hsa_circ_130294,RMVar_hsa_circ_127671,RMVar_hsa_circ_130296,RMVar_hsa_circ_105126,RMVar_hsa_circ_105497,RMVar_hsa_circ_130297,RMVar_hsa_circ_130298,RMVar_hsa_circ_124401,RMVar_hsa_circ_81313,RMVar_hsa_circ_85041,RMVar_hsa_circ_95249,RMVar_hsa_circ_127506,RMVar_hsa_circ_130299,RMVar_hsa_circ_130300,RMVar_hsa_circ_117100,RMVar_hsa_circ_130301,RMVar_hsa_circ_111690,RMVar_hsa_circ_126512,RMVar_hsa_circ_130303,RMVar_hsa_circ_130304,RMVar_hsa_circ_130302,RMVar_hsa_circ_112358,RMVar_hsa_circ_115274,RMVar_hsa_circ_130308,RMVar_hsa_circ_130309,RMVar_hsa_circ_130307,RMVar_hsa_circ_130310,RMVar_hsa_circ_116992,RMVar_hsa_circ_126705,RMVar_hsa_circ_130312,RMVar_hsa_circ_97024,RMVar_hsa_circ_130313,RMVar_hsa_circ_130314,RMVar_hsa_circ_104140,RMVar_hsa_circ_17516,RMVar_hsa_circ_102017,RMVar_hsa_circ_106377,RMVar_hsa_circ_130315,RMVar_hsa_circ_130316,RMVar_hsa_circ_81525,RMVar_hsa_circ_115015,RMVar_hsa_circ_130318,RMVar_hsa_circ_104207,RMVar_hsa_circ_130319,RMVar_hsa_circ_130320,RMVar_hsa_circ_130321 110758 RMVar_ID_110758 Human_SNP_ID_804079345 m1A Human chr1 + 151008590 151008590 151008590 TTCGTCGGGGAAACCTCTCCTCGACCAGGGGCACCTCTACTCGACCAGGGGCGACGGCGTACTTT TTCGTCGGGGAAACCTCTCCTCGACCAGGGGCTCCTCTACTCGACCAGGGGCGACGGCGTACTTT A T PRUNE1 Ensembl:ENSG00000143363 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr1:151008461..151008685;chr1:151008451..151008650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_3992693 Human_Splice_Rec_128005,Human_Splice_Rec_128017,Human_Splice_Rec_128031,Human_Splice_Rec_128041,Human_Splice_Rec_128057,Human_Splice_Rec_128067,Human_Splice_Rec_128077,Human_Splice_Rec_128083,Human_Splice_Rec_128091,Human_Splice_Rec_128103 110759 RMVar_ID_110759 Human_SNP_ID_804079538 m1A Human chr1 + 16393272 16393272 16393272 ATCTCCTCCCAAAGTGCCCATTGTGATTCAGGACGATAGCCTTCCCGCGGGGCCCCCTCCACAGA ATCTCCTCCCAAAGTGCCCATTGTGATTCAGGGCGATAGCCTTCCCGCGGGGCCCCCTCCACAGA A G SZRD1 Ensembl:ENSG00000055070 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:16391351..16393426 26863196 MeRIP-seq:(Medium) rs1212506179 Functional Loss SNV TCGA 33..33 33 UCS 1 - Human_RBP_ID_331541,Human_RBP_ID_1414892,Human_RBP_ID_3285328,Human_RBP_ID_4084329,Human_RBP_ID_5707000,Human_RBP_ID_8289345,Human_RBP_ID_10637738,Human_RBP_ID_18186861,Human_RBP_ID_18555250,Human_RBP_ID_22486316,Human_RBP_ID_26310315,Human_RBP_ID_26846098,Human_RBP_ID_27171112 Human_Splice_Rec_22112,Human_Splice_Rec_22116,Human_Splice_Rec_22120,Human_Splice_Rec_22128,Human_Splice_Rec_22134,Human_Splice_Rec_22142,Human_Splice_Rec_22148,Human_Splice_Rec_22156,Human_Splice_Rec_22160,Human_Splice_Rec_22166 RMVar_hsa_circ_46115,RMVar_hsa_circ_24913 110760 RMVar_ID_110760 Human_SNP_ID_804095031 m1A Human chr1 + 154328052 154328052 154328052 AAGAGGGTCTTCAAAAGAGGTCTCATGAGGGGAGGGAAGGGTTATCCTCAGCTTCCTGACCTCAT AAGAGGGTCTTCAAAAGAGGTCTCATGAGGGGCGGGAAGGGTTATCCTCAGCTTCCTGACCTCAT A C ATP8B2 Ensembl:ENSG00000143515 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154328051..154328122 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110761 RMVar_ID_110761 Human_SNP_ID_804110919 m1A Human chr1 - 25228999 25228998 25228999 GGAGTGGGAACTAAAGGAAGAGGAAAAGAAAAAGGTTAGGAACTATTCTATCTTCATAAGTGATT GGAGTGGGAACTAAAGGAAGAGGAAAAGAAAA_GGTTAGGAACTATTCTATCTTCATAAGTGATT CT C SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:25227451..25230361 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_22874682,Human_RBP_ID_24541774,Human_RBP_ID_26310544,Human_RBP_ID_27797601 Human_Splice_Rec_31971 RMVar_hsa_circ_52219,RMVar_hsa_circ_67009 110762 RMVar_ID_110762 Human_SNP_ID_804128586 m1A Human chr1 - 178542955 178542931 178542955 TGGGTGGGCCTCTCACCCCAGACGGCGGCCGCAGCCCGTCCCTGATCACCGGCCGCCTGAGCCCT TGGGTGGGCCTCTCACCCCAGACGGCGGCCGC________________________CTGAGCCCT GGCGGCCGGTGATCAGGGACGGGCT G lnc-CLEC20A-8 RNACentral:URS00008B98C7 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:178542915..178542986 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..56 33 OV 1 - 110763 RMVar_ID_110763 Human_SNP_ID_804154863 m1A Human chr1 + 65592830 65592830 65592830 TTTGAAAATCACATCTGGTGGAGTAATTTTCCAGTCACCTCTAATGTCAGTTCAGCCCATAAATA TTTGAAAATCACATCTGGTGGAGTAATTTTCCGGTCACCTCTAATGTCAGTTCAGCCCATAAATA A G LEPR Ensembl:ENSG00000116678 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137101 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,pancreas ductal_carcinoma,COCA,large_intestine adenocarcinoma 29 pancreas,head and neck,large intestine Human_RBP_ID_979450 Human_Splice_Rec_82851,Human_Splice_Rec_82889,Human_Splice_Rec_82927,Human_Splice_Rec_82963,Human_Splice_Rec_82987,Human_Splice_Rec_83023,Human_Splice_Rec_83057 Human_miRNA_ID_250040,Human_miRNA_ID_820188,Human_miRNA_ID_2346835 Clinvar_Rec_275 GWAS_ID_8132,GWAS_ID_8133,GWAS_ID_8134,GWAS_ID_8135,GWAS_ID_8136,GWAS_ID_8137,GWAS_ID_8138,GWAS_ID_8139,GWAS_ID_8140,GWAS_ID_8141,GWAS_ID_8142,GWAS_ID_8143,GWAS_ID_8144,GWAS_ID_8145,GWAS_ID_8146,GWAS_ID_8147,GWAS_ID_8148,GWAS_ID_8149,GWAS_ID_8150,GWAS_ID_8151,GWAS_ID_8152,GWAS_ID_8153,GWAS_ID_8154,GWAS_ID_8155,GWAS_ID_8156,GWAS_ID_8157,GWAS_ID_8158,GWAS_ID_8159,GWAS_ID_8160,GWAS_ID_8161,GWAS_ID_8162,GWAS_ID_8163,GWAS_ID_8164,GWAS_ID_8165,GWAS_ID_8166,GWAS_ID_8167,GWAS_ID_8168,GWAS_ID_8169,GWAS_ID_8170,GWAS_ID_8171,GWAS_ID_8172,GWAS_ID_8173,GWAS_ID_8174,GWAS_ID_8175,GWAS_ID_8176,GWAS_ID_8177,GWAS_ID_8178,GWAS_ID_8179,GWAS_ID_8180,GWAS_ID_8181,GWAS_ID_8182,GWAS_ID_8183,GWAS_ID_8184,GWAS_ID_8185,GWAS_ID_8186,GWAS_ID_8187,GWAS_ID_8188,GWAS_ID_8189,GWAS_ID_8190,GWAS_ID_8191,GWAS_ID_8192,GWAS_ID_8193,GWAS_ID_8194,GWAS_ID_8195,GWAS_ID_8196,GWAS_ID_8197,GWAS_ID_8198,GWAS_ID_8199,GWAS_ID_8200,GWAS_ID_8201,GWAS_ID_8202,GWAS_ID_8203,GWAS_ID_8204,GWAS_ID_8205,GWAS_ID_8206,GWAS_ID_8207,GWAS_ID_8208,GWAS_ID_8209,GWAS_ID_8210,GWAS_ID_8211,GWAS_ID_8212,GWAS_ID_8213,GWAS_ID_8214,GWAS_ID_8215 RMVar_hsa_circ_106328,RMVar_hsa_circ_133704,RMVar_hsa_circ_6206,RMVar_hsa_circ_10323,RMVar_hsa_circ_331632,RMVar_hsa_circ_120263,RMVar_hsa_circ_60486,RMVar_hsa_circ_356016,RMVar_hsa_circ_133709,RMVar_hsa_circ_61633,RMVar_hsa_circ_14004,RMVar_hsa_circ_68766,RMVar_hsa_circ_350358,RMVar_hsa_circ_356483,RMVar_hsa_circ_366373,RMVar_hsa_circ_91754,RMVar_hsa_circ_133710 110764 RMVar_ID_110764 Human_SNP_ID_804162385 m1A Human chr1 + 119177816 119177816 119177816 ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGAGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT ACAGAGAAAGAGACAGAGAGAGGAAGAAACAGGGAGTCAAAGAGAAAGAGACAAAGAGAAGGAGT A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:119177716..119177863 26863196 MeRIP-seq:(Medium) rs12067751 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5245402 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 110765 RMVar_ID_110765 Human_SNP_ID_804164412 m1A Human chr1 - 226186655 226186655 226186655 CAGCAGCCGGAGATGGCGGCGGTGCTGAACGCAGAGCGACTCGAGGTGTCCGTCGACGGCCTCAC CAGCAGCCGGAGATGGCGGCGGTGCTGAACGCGGAGCGACTCGAGGTGTCCGTCGACGGCCTCAC T C ACBD3 Ensembl:ENSG00000182827 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:226165943..226186750;chr1:226186357..226186730;chr1:226186526..226186750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_1422500,Human_RBP_ID_4028521,Human_RBP_ID_8744171,Human_RBP_ID_9270671,Human_RBP_ID_9359907,Human_RBP_ID_22871069 110766 RMVar_ID_110766 Human_SNP_ID_804167051 m1A Human chr1 + 200409658 200409658 200409658 CTACCACCGCCGCCGGAGCCGCTACCACCGCTACTGCCGGTACCTCCGCCGCCACTCAGGAACCC CTACCACCGCCGCCGGAGCCGCTACCACCGCTTCTGCCGGTACCTCCGCCGCCACTCAGGAACCC A T AC104461.1 Ensembl:ENSG00000230623 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr1:200409583..200409684 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 110767 RMVar_ID_110767 Human_SNP_ID_804177091 m1A Human chr1 + 23787376 23787376 23787376 CAGGTTACCCCACAGACACACTTTATTTCCTAAGGGCTGGCCAAGGCTCCCATAGAGGCGCTGTG CAGGTTACCCCACAGACACACTTTATTTCCTATGGGCTGGCCAAGGCTCCCATAGAGGCGCTGTG A T PITHD1 Ensembl:ENSG00000057757 Protein coding stop codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:23787326..23787375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_17114,Human_RBP_ID_347936,Human_RBP_ID_976557,Human_RBP_ID_5790865,Human_RBP_ID_8304429,Human_RBP_ID_8746464,Human_RBP_ID_9355721,Human_RBP_ID_10867889,Human_RBP_ID_17216998,Human_RBP_ID_17745169,Human_RBP_ID_22427001,Human_RBP_ID_24666182,Human_RBP_ID_27396008,Human_RBP_ID_27591095 Human_miRNA_ID_2001053,Human_miRNA_ID_2002438,Human_miRNA_ID_2216580,Human_miRNA_ID_2396616 RMVar_hsa_circ_106493,RMVar_hsa_circ_88041,RMVar_hsa_circ_130497,RMVar_hsa_circ_76190,RMVar_hsa_circ_130498,RMVar_hsa_circ_130499 110768 RMVar_ID_110768 Human_SNP_ID_804186532 m1A Human chr1 - 1534019 1534019 1534019 CCCACGCCCAGGCCCTTCCGCCTTCAGCCAGCACATCTTCTGCTGGTGCTGCTGGACAGCATCTT CCCACGCCCAGGCCCTTCCGCCTTCAGCCAGCGCATCTTCTGCTGGTGCTGCTGGACAGCATCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1533981..1534124 26863196 MeRIP-seq:(Medium) rs41285842 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 6 lung Human_RBP_ID_1249970 110769 RMVar_ID_110769 Human_SNP_ID_804191282 m1A Human chr1 + 151118021 151118021 151118021 ACTCCAGGAGGCCAATCGAAGAGCCCAGGAATACCGACACCAGCTCCTAAAGAAAGAGCAGGAAG ACTCCAGGAGGCCAATCGAAGAGCCCAGGAATGCCGACACCAGCTCCTAAAGAAAGAGCAGGAAG A G GABPB2 Ensembl:ENSG00000143458 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:151117940..151118032 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_Splice_Rec_128296,Human_Splice_Rec_128330,Human_Splice_Rec_128336 RMVar_hsa_circ_19016,RMVar_hsa_circ_288996,RMVar_hsa_circ_267228,RMVar_hsa_circ_136021,RMVar_hsa_circ_340094,RMVar_hsa_circ_300384,RMVar_hsa_circ_136030,RMVar_hsa_circ_136033,RMVar_hsa_circ_136034,RMVar_hsa_circ_330561,RMVar_hsa_circ_309381,RMVar_hsa_circ_136035 110770 RMVar_ID_110770 Human_SNP_ID_804201787 m1A Human chr1 - 20715538 20715538 20715538 ATGCAGGGCCTGCCGGATCCGCCCTCCCAGAGAGGCATCATCCCCAGGGCCTTCGAGCACGTGTT ATGCAGGGCCTGCCGGATCCGCCCTCCCAGAGGGGCATCATCCCCAGGGCCTTCGAGCACGTGTT T C KIF17 Ensembl:ENSG00000117245 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:20715534..20715621 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THYM 1 - Human_Splice_Rec_26535,Human_Splice_Rec_26563,Human_Splice_Rec_26591 RMVar_hsa_circ_31788,RMVar_hsa_circ_12100,RMVar_hsa_circ_285825,RMVar_hsa_circ_129870 110771 RMVar_ID_110771 Human_SNP_ID_804204925 m1A Human chr1 + 211207859 211207859 211207859 ACAGAGAAGGCCAAGGACCTCGCCAGCAAGGCAGCCACCAAGAAGCAGCAGCAGCAGCAACAGTT ACAGAGAAGGCCAAGGACCTCGCCAGCAAGGCGGCCACCAAGAAGCAGCAGCAGCAGCAACAGTT A G AC092017.1 Ensembl:ENSG00000226986 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 110772 RMVar_ID_110772 Human_SNP_ID_804228596 m1A Human chr1 - 62253162 62253162 62253162 ACCATCAGAACAAAGCTGGCTACACTGCCGTAATGATCACTCCCTTGGCTTCCGCAGAGACCAAT ACCATCAGAACAAAGCTGGCTACACTGCCGTAGTGATCACTCCCTTGGCTTCCGCAGAGACCAAT T C KANK4 Ensembl:ENSG00000132854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62253116..62253247 26863196 MeRIP-seq:(Medium) rs755326990 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 6 lung Human_Splice_Rec_79262,Human_Splice_Rec_79263,Human_Splice_Rec_79268,Human_Splice_Rec_79269,Human_Splice_Rec_79280,Human_Splice_Rec_79281,Human_Splice_Rec_79296,Human_Splice_Rec_79297 RMVar_hsa_circ_18709,RMVar_hsa_circ_373374,RMVar_hsa_circ_374370,RMVar_hsa_circ_335173,RMVar_hsa_circ_133482,RMVar_hsa_circ_133483,RMVar_hsa_circ_133484,RMVar_hsa_circ_13068 110773 RMVar_ID_110773 Human_SNP_ID_804246192 m1A Human chr1 + 214334294 214334294 214334294 ACATGGGCCTGGAACACAAAGCCGCAGGGGAGAAAGCCCTGAAGAAGGTATGTCTGTAACTCGGC ACATGGGCCTGGAACACAAAGCCGCAGGGGAGGAAGCCCTGAAGAAGGTATGTCTGTAACTCGGC A G SMYD2 Ensembl:ENSG00000143499 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:214334191..214336782 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_18966407 Human_Splice_Rec_187245,Human_Splice_Rec_187263,Human_Splice_Rec_187282,Human_Splice_Rec_187283,Human_Splice_Rec_187300,Human_Splice_Rec_187301 RMVar_hsa_circ_335993,RMVar_hsa_circ_110312,RMVar_hsa_circ_139550,RMVar_hsa_circ_139548,RMVar_hsa_circ_139547,RMVar_hsa_circ_139553,RMVar_hsa_circ_139554,RMVar_hsa_circ_139555 110774 RMVar_ID_110774 Human_SNP_ID_804254623 m1A Human chr1 - 153561590 153561590 153561590 TGGTGATGAGTGTATTTCCTGTCACTTTCAGGAGAAAGTGGATGAGGAGGGGCTGAAGAAGCTGA TGGTGATGAGTGTATTTCCTGTCACTTTCAGGTGAAAGTGGATGAGGAGGGGCTGAAGAAGCTGA T A S100A2 Ensembl:ENSG00000196754 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153561563..153561628 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 13 oesophagus Human_Splice_Rec_131756,Human_Splice_Rec_131758,Human_Splice_Rec_131762,Human_Splice_Rec_131766,Human_Splice_Rec_131770 RMVar_hsa_circ_95455,RMVar_hsa_circ_136214,RMVar_hsa_circ_81760,RMVar_hsa_circ_136213 110775 RMVar_ID_110775 Human_SNP_ID_804287960 m1A Human chr1 + 23310675 23310675 23310675 GCCTCCTACATTGCCCCCACGATTGCCCCGAGATCCACGGGAACCACGGCCTCTCTGCTGTTGAG GCCTCCTACATTGCCCCCACGATTGCCCCGAGCTCCACGGGAACCACGGCCTCTCTGCTGTTGAG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:23310590..23310951 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma,large_intestine adenocarcinoma 12 head and neck,large intestine 110776 RMVar_ID_110776 Human_SNP_ID_804293588 m1A Human chr1 + 161120525 161120525 161120525 GCCCAGGTGTTGCTGCGGGCCCGTGCTATCGAAACCCAGTGCTATGTAGTGGCAGCAGCACAGTG GCCCAGGTGTTGCTGCGGGCCCGTGCTATCGACACCCAGTGCTATGTAGTGGCAGCAGCACAGTG A C NIT1 Ensembl:ENSG00000158793 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:161119508..161120534 32194978 MeRIP-seq:(Medium) rs1456915436 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 4 oesophagus Human_Splice_Rec_149580,Human_Splice_Rec_149602,Human_Splice_Rec_149624,Human_Splice_Rec_149652,Human_Splice_Rec_149666 110777 RMVar_ID_110777 Human_SNP_ID_804305798 m1A Human chr1 - 9734903 9734903 9734903 GTGGGGCGCGGGCTCCCTCGCCTCGGCCGGAAACCCCATTGTCCCCATGTACTTGGCGGGGCTCT GTGGGGCGCGGGCTCCCTCGCCTCGGCCGGAAGCCCCATTGTCCCCATGTACTTGGCGGGGCTCT T C CLSTN1 Ensembl:ENSG00000171603 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:9734901..9735059 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_85258,RMVar_hsa_circ_121065,RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_128821,RMVar_hsa_circ_128822,RMVar_hsa_circ_15648,RMVar_hsa_circ_91160,RMVar_hsa_circ_15408,RMVar_hsa_circ_128824 110778 RMVar_ID_110778 Human_SNP_ID_804310349 m1A Human chr1 + 227924297 227924297 227924297 CAGGCCTCACGGTTCTCCAGGTCGGGTGCCTCATCGCAGGTACAGCGCTCCATGCGGCCCGCGCT CAGGCCTCACGGTTCTCCAGGTCGGGTGCCTCGTCGCAGGTACAGCGCTCCATGCGGCCCGCGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:227924247..227924320 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine 110779 RMVar_ID_110779 Human_SNP_ID_804339631 m1A Human chr1 + 44777650 44777650 44777650 TACTCGTAAAACAAGGATCATCGATGTTGTCTACAATGCATCTAATAACGAGCTGGTTCGTACCA TACTCGTAAAACAAGGATCATCGATGTTGTCTGCAATGCATCTAATAACGAGCTGGTTCGTACCA A G RPS8 Ensembl:ENSG00000142937 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:44777616..44777930 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_356244,Human_RBP_ID_1432074,Human_RBP_ID_1748761,Human_RBP_ID_2149544,Human_RBP_ID_3314276,Human_RBP_ID_4096631,Human_RBP_ID_8312486,Human_RBP_ID_8980889,Human_RBP_ID_17678042,Human_RBP_ID_18576049,Human_RBP_ID_22144094,Human_RBP_ID_22785168,Human_RBP_ID_24452963,Human_RBP_ID_26380745,Human_RBP_ID_26798305,Human_RBP_ID_26865589,Human_RBP_ID_27183941,Human_RBP_ID_27399296 Human_Splice_Rec_62124,Human_Splice_Rec_62132,Human_Splice_Rec_62142,Human_Splice_Rec_62154,Human_Splice_Rec_62163 Human_miRNA_ID_2444761,Human_miRNA_ID_2446144 RMVar_hsa_circ_97389,RMVar_hsa_circ_115120,RMVar_hsa_circ_117122,RMVar_hsa_circ_132426,RMVar_hsa_circ_132427,RMVar_hsa_circ_354694,RMVar_hsa_circ_114196,RMVar_hsa_circ_132428,RMVar_hsa_circ_50883,RMVar_hsa_circ_75992,RMVar_hsa_circ_103338,RMVar_hsa_circ_132430,RMVar_hsa_circ_92960,RMVar_hsa_circ_132432,RMVar_hsa_circ_132433,RMVar_hsa_circ_132431 110780 RMVar_ID_110780 Human_SNP_ID_804380651 m1A Human chr1 - 234478574 234478574 234478574 CGCCGTCGCCCTGGCGCTGGGCGGGGGCGGGGACGGGGATGAGGCCGGGCCTGCCGAGGACGCGG CGCCGTCGCCCTGGCGCTGGGCGGGGGCGGGGGCGGGGATGAGGCCGGGCCTGCCGAGGACGCGG T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr1:234478275..234478625;chr1:234478151..234479140 26863196 MeRIP-seq:(Medium) rs1469394116 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_223537,Human_RBP_ID_801745,Human_RBP_ID_3328920,Human_RBP_ID_5312023,Human_RBP_ID_8724708,Human_RBP_ID_8754482,Human_RBP_ID_9319464,Human_RBP_ID_9410742,Human_RBP_ID_17099952,Human_RBP_ID_18455759,Human_RBP_ID_18474426,Human_RBP_ID_22026568 110781 RMVar_ID_110781 Human_SNP_ID_804380710 m1A Human chr1 + 113940394 113940394 113940394 CTTCCTTTCTCTCAATATAGGTATGGCATCACAGCTGCAAGTGTTTTCGCCCCCATCAGTGTCGT CTTCCTTTCTCTCAATATAGGTATGGCATCACTGCTGCAAGTGTTTTCGCCCCCATCAGTGTCGT A T HIPK1 Ensembl:ENSG00000163349 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:113940376..113940400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_18187768 Human_Splice_Rec_112060,Human_Splice_Rec_112086,Human_Splice_Rec_112110,Human_Splice_Rec_112134,Human_Splice_Rec_112160,Human_Splice_Rec_112186,Human_Splice_Rec_112212,Human_Splice_Rec_112218 Human_miRNA_ID_2011139,Human_miRNA_ID_2757491 RMVar_hsa_circ_81168,RMVar_hsa_circ_21870,RMVar_hsa_circ_100526,RMVar_hsa_circ_345619,RMVar_hsa_circ_135511,RMVar_hsa_circ_275186,RMVar_hsa_circ_43393,RMVar_hsa_circ_135512,RMVar_hsa_circ_135513,RMVar_hsa_circ_135514 110782 RMVar_ID_110782 Human_SNP_ID_804397815 m1A Human chr1 - 36177934 36177934 36177934 AGGCAGAGTGTGGCCTGGCCCTGGGCTGGGGCAGGGGGAGGCAGGCCTGTGCCAGGATGTGGAGG AGGCAGAGTGTGGCCTGGCCCTGGGCTGGGGCTGGGGGAGGCAGGCCTGTGCCAGGATGTGGAGG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:36177856..36177982 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 110783 RMVar_ID_110783 Human_SNP_ID_804401520 m1A Human chr1 - 26729851 26729850 26729852 TAATCACAATCACCATCTACCTGCTGTGTATAAGAGAGGCCGCCCATGGCACTCTGCGCCCGGCC TAATCACAATCACCATCTACCTGCTGTGTAT__GAGAGGCCGCCCATGGCACTCTGCGCCCGGCC CTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:26729611..26729909 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 LICA 1 - 110784 RMVar_ID_110784 Human_SNP_ID_804408118 m1A Human chr1 + 156077366 156077366 156077366 AACACGGGGTCGCGGTCACGGCTTGGTGTGATAATGTATGTGTTGGTTTGCTGCTGGATGCGCTT AACACGGGGTCGCGGTCACGGCTTGGTGTGATCATGTATGTGTTGGTTTGCTGCTGGATGCGCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156077357..156077425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110785 RMVar_ID_110785 Human_SNP_ID_804410117 m1A Human chr1 + 206728806 206728806 206728806 CGCACATCGTACGGATCGTGGATGTGTACGAGAATCTGTACGCAGGGAGGAAGTGCCTGCTGATT CGCACATCGTACGGATCGTGGATGTGTACGAGTATCTGTACGCAGGGAGGAAGTGCCTGCTGATT A T MAPKAPK2 Ensembl:ENSG00000162889 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:206728756..206728889 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_272261,Human_RBP_ID_1734197,Human_RBP_ID_17223076,Human_RBP_ID_23358901,Human_RBP_ID_26312601 Human_Splice_Rec_181166,Human_Splice_Rec_181167,Human_Splice_Rec_181184,Human_Splice_Rec_181185 RMVar_hsa_circ_11824,RMVar_hsa_circ_42935,RMVar_hsa_circ_99465,RMVar_hsa_circ_139257,RMVar_hsa_circ_370178,RMVar_hsa_circ_38006,RMVar_hsa_circ_139258 110786 RMVar_ID_110786 Human_SNP_ID_804415162 m1A Human chr1 + 108808879 108808879 108808879 GGATAAAGTCTCCTTAATTAAAGATGAATAGCATTTCTTTTTGGAGGGTTTAGAGATTCTTACTA GGATAAAGTCTCCTTAATTAAAGATGAATAGCGTTTCTTTTTGGAGGGTTTAGAGATTCTTACTA A G STXBP3 Ensembl:ENSG00000116266 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1149154 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_Splice_Rec_104578 110787 RMVar_ID_110787 Human_SNP_ID_804416298 m1A Human chr1 + 20969567 20969567 20969567 CCTCCAGACATAATCTCCTCTGTTATGTCTTTACCTCCCTGGTTTGGATCCCGAATTCTTATCTA CCTCCAGACATAATCTCCTCTGTTATGTCTTTGCCTCCCTGGTTTGGATCCCGAATTCTTATCTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:20969427..20969641 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 8 uterus 110788 RMVar_ID_110788 Human_SNP_ID_804422473 m1A Human chr1 + 201829227 201829227 201829227 CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCAGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT CTGAGGGGAGAAAAGATGGCGGCGGCGGCGGCGGCTGGTGCGGCCTCCGGGCTGCCGGGTCCAGT A G IPO9 Ensembl:ENSG00000198700 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:201829151..201829563;chr1:201829140..201829510 26863196 MeRIP-seq:(Medium) rs1042568436 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_223155,Human_RBP_ID_744423,Human_RBP_ID_803537,Human_RBP_ID_4016664,Human_RBP_ID_9320307,Human_RBP_ID_18415128 Human_miRNA_ID_2240141,Human_miRNA_ID_2576970 RMVar_hsa_circ_84187,RMVar_hsa_circ_138839 110789 RMVar_ID_110789 Human_SNP_ID_804427568 m1A Human chr1 + 241866849 241866849 241866849 TTTCCTTTTCTAGCCTGCCCATTCAAGAAGTCATAGTTGGGATGACAAAACATGTCAAAAGTCAG TTTCCTTTTCTAGCCTGCCCATTCAAGAAGTCGTAGTTGGGATGACAAAACATGTCAAAAGTCAG A G EXO1 Ensembl:ENSG00000174371 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs735943 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,pancreas ductal_carcinoma,COCA,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 13 pancreas,haematopoietic and lymphoid tissue,breast Human_RBP_ID_1426131,Human_RBP_ID_8746666,Human_RBP_ID_10869628,Human_RBP_ID_18568676,Human_RBP_ID_21908409,Human_RBP_ID_22783236,Human_RBP_ID_23378084,Human_RBP_ID_27591280,Human_RBP_ID_27799423 Human_Splice_Rec_205866,Human_Splice_Rec_205908,Human_Splice_Rec_205934 GWAS_ID_12778,GWAS_ID_12779,GWAS_ID_12780,GWAS_ID_12781,GWAS_ID_12782,GWAS_ID_12783,GWAS_ID_12784 RMVar_hsa_circ_141087,RMVar_hsa_circ_95280,RMVar_hsa_circ_365720,RMVar_hsa_circ_51137,RMVar_hsa_circ_37847,RMVar_hsa_circ_4424,RMVar_hsa_circ_141088,RMVar_hsa_circ_365825,RMVar_hsa_circ_68461,RMVar_hsa_circ_312008 110790 RMVar_ID_110790 Human_SNP_ID_804436912 m1A Human chr1 + 26731360 26731360 26731360 ACAGCTCCAGTCCTCTCAGCCTCCATACTCCCAGCAGCCATCCCAGCCTCCACATCAGCAGTCCC ACAGCTCCAGTCCTCTCAGCCTCCATACTCCCGGCAGCCATCCCAGCCTCCACATCAGCAGTCCC A G ARID1A Ensembl:ENSG00000117713 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:26731186..26732708 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_5125224,Human_RBP_ID_17217577,Human_RBP_ID_17338003,Human_RBP_ID_17456205,Human_RBP_ID_18928128,Human_RBP_ID_22140266,Human_RBP_ID_22532083,Human_RBP_ID_26313681,Human_RBP_ID_27396804 Human_miRNA_ID_2712099,Human_miRNA_ID_3048087 RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_268846,RMVar_hsa_circ_272963,RMVar_hsa_circ_130681,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_116238,RMVar_hsa_circ_130683 110791 RMVar_ID_110791 Human_SNP_ID_804440378 m1A Human chr1 + 244855917 244855917 244855917 ACACTCAAAATTAACTTGCCTCCTCCTCTGAAATTTCCACCACGCATATTGAATCCTCCACGTCC ACACTCAAAATTAACTTGCCTCCTCCTCTGAAGTTTCCACCACGCATATTGAATCCTCCACGTCC A G NONHSAG004867.2 RNACentral:URS00009B46E1 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:244855901..244856000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 15 pancreas 110792 RMVar_ID_110792 Human_SNP_ID_804442607 m1A Human chr1 - 218302552 218302552 218302552 CTACAAGAGAACTGGTGGAACATACCTGTTTTATTTTCTCTAGTCTTTCTTGCTTTAACTTTTCT CTACAAGAGAACTGGTGGAACATACCTGTTTTCTTTTCTCTAGTCTTTCTTGCTTTAACTTTTCT T G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:218302513..218302642 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - 110793 RMVar_ID_110793 Human_SNP_ID_804445707 m1A Human chr1 - 156744224 156744223 156744224 CAGCGACGAGGAAGGGAAGCTGGTCATTGATGAGCCAGCCAAGGAGAAGAACGAGAAAGGAGCGT CAGCGACGAGGAAGGGAAGCTGGTCATTGATG_GCCAGCCAAGGAGAAGAACGAGAAAGGAGCGT CT C HDGF Ensembl:ENSG00000143321 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156744151..156744225 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LICA 1 - Human_RBP_ID_20979,Human_RBP_ID_329083,Human_RBP_ID_801780,Human_RBP_ID_971826,Human_RBP_ID_1413615,Human_RBP_ID_1727102,Human_RBP_ID_2097227,Human_RBP_ID_4000240,Human_RBP_ID_5697614,Human_RBP_ID_8287621,Human_RBP_ID_8956848,Human_RBP_ID_10609777,Human_RBP_ID_18966129,Human_RBP_ID_23336953,Human_RBP_ID_24541524,Human_RBP_ID_26312031,Human_RBP_ID_26386576,Human_RBP_ID_26844135 Human_Splice_Rec_143605,Human_Splice_Rec_143615,Human_Splice_Rec_143625,Human_Splice_Rec_143639,Human_Splice_Rec_143649,Human_Splice_Rec_143653,Human_Splice_Rec_143661,Human_Splice_Rec_143673,Human_Splice_Rec_143683,Human_Splice_Rec_143689 Human_miRNA_ID_2082216,Human_miRNA_ID_2216724 RMVar_hsa_circ_82179,RMVar_hsa_circ_117608,RMVar_hsa_circ_108690,RMVar_hsa_circ_115770,RMVar_hsa_circ_99168,RMVar_hsa_circ_62751,RMVar_hsa_circ_136902,RMVar_hsa_circ_136904,RMVar_hsa_circ_136905,RMVar_hsa_circ_136903,RMVar_hsa_circ_136901,RMVar_hsa_circ_361976,RMVar_hsa_circ_65078 110794 RMVar_ID_110794 Human_SNP_ID_804451547 m1A Human chr1 + 154259027 154259027 154259027 GATGACTTGCAGATGCTTCAGACAAGATTTCCATTGGTGAGTATGTGGGATAGAGCTTTGGAAAA GATGACTTGCAGATGCTTCAGACAAGATTTCCCTTGGTGAGTATGTGGGATAGAGCTTTGGAAAA A C UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154258964..154259769 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THYM 1 - Human_RBP_ID_1726159,Human_RBP_ID_10591842,Human_RBP_ID_19039253,Human_RBP_ID_22847381 Human_Splice_Rec_133914,Human_Splice_Rec_133915,Human_Splice_Rec_133960,Human_Splice_Rec_133961,Human_Splice_Rec_134006,Human_Splice_Rec_134007,Human_Splice_Rec_134102,Human_Splice_Rec_134103,Human_Splice_Rec_134182,Human_Splice_Rec_134183,Human_Splice_Rec_134208,Human_Splice_Rec_134209,Human_Splice_Rec_134224,Human_Splice_Rec_134225,Human_Splice_Rec_134240,Human_Splice_Rec_134241,Human_Splice_Rec_134257,Human_Splice_Rec_134263 RMVar_hsa_circ_356443,RMVar_hsa_circ_50165,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_11572,RMVar_hsa_circ_49077,RMVar_hsa_circ_89708,RMVar_hsa_circ_82305,RMVar_hsa_circ_136379,RMVar_hsa_circ_136381,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_106731,RMVar_hsa_circ_136389,RMVar_hsa_circ_85902,RMVar_hsa_circ_136392,RMVar_hsa_circ_98499,RMVar_hsa_circ_106489,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_324255,RMVar_hsa_circ_136398,RMVar_hsa_circ_136400,RMVar_hsa_circ_136401,RMVar_hsa_circ_86658,RMVar_hsa_circ_83774,RMVar_hsa_circ_126027,RMVar_hsa_circ_118289,RMVar_hsa_circ_136404,RMVar_hsa_circ_136406,RMVar_hsa_circ_127313,RMVar_hsa_circ_106934,RMVar_hsa_circ_136407,RMVar_hsa_circ_371668,RMVar_hsa_circ_136408,RMVar_hsa_circ_136409,RMVar_hsa_circ_272021,RMVar_hsa_circ_101381,RMVar_hsa_circ_111655,RMVar_hsa_circ_96950,RMVar_hsa_circ_136411,RMVar_hsa_circ_136413,RMVar_hsa_circ_136415,RMVar_hsa_circ_66134,RMVar_hsa_circ_136414,RMVar_hsa_circ_136412,RMVar_hsa_circ_136410 110795 RMVar_ID_110795 Human_SNP_ID_804456349 m1A Human chr1 - 150811479 150811459 150811479 ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGCGCACACATGCT ACATGTGAGTAAGTGAGAGAGAGTGTGTGTGT____________________GCGCACACATGCT CACACACACACACACACACAT C ARNT Ensembl:ENSG00000143437 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..52 33 LICA 1 - Human_RBP_ID_325807,Human_RBP_ID_1071435,Human_RBP_ID_5136352,Human_RBP_ID_5278532,Human_RBP_ID_22779913,Human_RBP_ID_23205328,Human_RBP_ID_23331604,Human_RBP_ID_26368095 110796 RMVar_ID_110796 Human_SNP_ID_804464740 m1A Human chr1 + 114510877 114510877 114510877 CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCACCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC CAGCCTGGGCCGAGCCCGAGGAGGCCGCGGCCGCCCCCCCGTCGTCGGGCCCGGCCGCGCCGCCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:114510826..114511048 26863196 MeRIP-seq:(Medium) rs6691166 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia 3 haematopoietic and lymphoid tissue 110797 RMVar_ID_110797 Human_SNP_ID_804464912 m1A Human chr1 + 50970411 50970411 50970411 CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCCAGGGGGGACCTAGAGCAACTTACTAGTTTGTTG CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCCTGGGGGGACCTAGAGCAACTTACTAGTTTGTTG A T CDKN2C Ensembl:ENSG00000123080 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:50970251..50970455 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_5836072,Human_RBP_ID_17753373,Human_RBP_ID_26388203 Human_Splice_Rec_68556,Human_Splice_Rec_68557,Human_Splice_Rec_68560,Human_Splice_Rec_68561,Human_Splice_Rec_68563 RMVar_hsa_circ_11687 110798 RMVar_ID_110798 Human_SNP_ID_804464918 m1A Human chr1 + 50970411 50970411 50970411 CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCCAGGGGGGACCTAGAGCAACTTACTAGTTTGTTG CTTGGGGGAACGAGTTGGCGTCCGCAGCTGCCCGGGGGGACCTAGAGCAACTTACTAGTTTGTTG A C CDKN2C Ensembl:ENSG00000123080 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:50970251..50970455 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_5836072,Human_RBP_ID_17753373,Human_RBP_ID_26388203 Human_Splice_Rec_68556,Human_Splice_Rec_68557,Human_Splice_Rec_68560,Human_Splice_Rec_68561,Human_Splice_Rec_68563 RMVar_hsa_circ_11687 110799 RMVar_ID_110799 Human_SNP_ID_804471443 m1A Human chr1 - 225519316 225519312 225519316 CGGCAGGAACGCCTGGATCGGGAGAGGCAAGAAAGACAAGAACGAGAGAGGCTGGAGAGACTGGA CGGCAGGAACGCCTGGATCGGGAGAGGCAAGA____CAAGAACGAGAGAGGCTGGAGAGACTGGA GTCTT G ENAH Ensembl:ENSG00000154380 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:225519201..225519575 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..36 33 LIHC 1 - Human_RBP_ID_21787,Human_RBP_ID_222446,Human_RBP_ID_1122853,Human_RBP_ID_8300132,Human_RBP_ID_9357575,Human_RBP_ID_10804460,Human_RBP_ID_18966443,Human_RBP_ID_22855967,Human_RBP_ID_23117582,Human_RBP_ID_23368192,Human_RBP_ID_24646126 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039,RMVar_hsa_circ_58926,RMVar_hsa_circ_365726,RMVar_hsa_circ_15278,RMVar_hsa_circ_358888,RMVar_hsa_circ_357389,RMVar_hsa_circ_120961,RMVar_hsa_circ_140042,RMVar_hsa_circ_94840,RMVar_hsa_circ_140043,RMVar_hsa_circ_373746,RMVar_hsa_circ_140044,RMVar_hsa_circ_67732,RMVar_hsa_circ_354688 110800 RMVar_ID_110800 Human_SNP_ID_804497183 m1A Human chr1 + 27914501 27914500 27914501 GCCGAGAAGGTGCGGGTCTGGGGGAATAGCGGAAAACCACAGAACGCGGCCGCCACTGCGCCGCT GCCGAGAAGGTGCGGGTCTGGGGGAATAGCGG_AAACCACAGAACGCGGCCGCCACTGCGCCGCT GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:27914186..27914550 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - 110801 RMVar_ID_110801 Human_SNP_ID_804508535 m1A Human chr1 + 32898199 32898199 32898199 ACTGCAGAGCCACCGCATCTTGAGGGGTGCCCACGTAGCGCAGCACTGTGCCATGGAACAGGGCA ACTGCAGAGCCACCGCATCTTGAGGGGTGCCCCCGTAGCGCAGCACTGTGCCATGGAACAGGGCA A C HPCA Ensembl:ENSG00000121905 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:32898126..32898325;chr1:32898126..32901243 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 110802 RMVar_ID_110802 Human_SNP_ID_804539289 m1A Human chr1 + 149977575 149977575 149977575 TAGGTAGAACATAGATCAAAATTCAGGCCTCCACCTGAGGAATAAATAAATACATAAGGCTCAAA TAGGTAGAACATAGATCAAAATTCAGGCCTCCTCCTGAGGAATAAATAAATACATAAGGCTCAAA A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:149971241..150010626 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - 110803 RMVar_ID_110803 Human_SNP_ID_804543571 m1A Human chr1 + 19311946 19311946 19311946 GTTCGGTGTGGCCGCGCTCCAGAAAGGCGCGCACGGCCGCGGCGCTGGCGGGCGCGTCCATGCGG GTTCGGTGTGGCCGCGCTCCAGAAAGGCGCGCGCGGCCGCGGCGCTGGCGGGCGCGTCCATGCGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:19311901..19312075 26863196 MeRIP-seq:(Medium) rs773343655 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 110804 RMVar_ID_110804 Human_SNP_ID_804543848 m1A Human chr1 - 171670653 171670653 171670653 CATGGATCTTCGTATACCAAGAGTACCGGTGGAGCCCCCACCTTCAATGTCACTGTCACCAAGAC CATGGATCTTCGTATACCAAGAGTACCGGTGGGGCCCCCACCTTCAATGTCACTGTCACCAAGAC T C PFN1P1 Ensembl:ENSG00000233328 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879022697 Functional Loss SNV ICGC 33..33 33 STAD 1 - 110805 RMVar_ID_110805 Human_SNP_ID_804558858 m1A Human chr1 - 186323768 186323768 186323768 AGCATCTGAAAGACAGGCCCCTCGAGCACCTCAGTCACCGAGACGCCCACCACATCCACTTCCCC AGCATCTGAAAGACAGGCCCCTCGAGCACCTCCGTCACCGAGACGCCCACCACATCCACTTCCCC T G TPR Ensembl:ENSG00000047410 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:186323718..186323800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_221009,Human_RBP_ID_9270513,Human_RBP_ID_18558360,Human_RBP_ID_24541296 Human_Splice_Rec_167151 Human_miRNA_ID_2036216,Human_miRNA_ID_2346915,Human_miRNA_ID_2872431,Human_miRNA_ID_2980397 RMVar_hsa_circ_3700,RMVar_hsa_circ_78732,RMVar_hsa_circ_99079,RMVar_hsa_circ_103104,RMVar_hsa_circ_75260,RMVar_hsa_circ_138425,RMVar_hsa_circ_138427,RMVar_hsa_circ_64852,RMVar_hsa_circ_138426,RMVar_hsa_circ_105287,RMVar_hsa_circ_123634,RMVar_hsa_circ_138430,RMVar_hsa_circ_365187,RMVar_hsa_circ_98048,RMVar_hsa_circ_120750,RMVar_hsa_circ_49811,RMVar_hsa_circ_93366,RMVar_hsa_circ_109808,RMVar_hsa_circ_115367,RMVar_hsa_circ_138432,RMVar_hsa_circ_138433,RMVar_hsa_circ_138434,RMVar_hsa_circ_114854,RMVar_hsa_circ_138438,RMVar_hsa_circ_94228,RMVar_hsa_circ_106047,RMVar_hsa_circ_27712,RMVar_hsa_circ_138439,RMVar_hsa_circ_138436,RMVar_hsa_circ_138437,RMVar_hsa_circ_138435,RMVar_hsa_circ_361923,RMVar_hsa_circ_123351,RMVar_hsa_circ_27630,RMVar_hsa_circ_82197,RMVar_hsa_circ_138440,RMVar_hsa_circ_138441,RMVar_hsa_circ_353475,RMVar_hsa_circ_59013,RMVar_hsa_circ_72903,RMVar_hsa_circ_19011,RMVar_hsa_circ_138442,RMVar_hsa_circ_138443 110806 RMVar_ID_110806 Human_SNP_ID_804561434 m1A Human chr1 - 12022262 12022262 12022262 GACTCCTGGTGCTGGCATTTGGCAGGTGGGAGAGAGGCCACCCCCGATCTGGCCACATCACGGAG GACTCCTGGTGCTGGCATTTGGCAGGTGGGAGGGAGGCCACCCCCGATCTGGCCACATCACGGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:12022211..12022379 26863196 MeRIP-seq:(Medium) rs745592384 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 110807 RMVar_ID_110807 Human_SNP_ID_804567027 m1A Human chr1 - 184754646 184754646 184754646 TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCATGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC TAGCAGCTGCGCGTGCGCGGAACCGCGGGGCCGTGAGCGAAGCCGGCGGCCGGGGCTGTGGGTCC T C EDEM3 Ensembl:ENSG00000116406 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:184754599..184754808 26863196 MeRIP-seq:(Medium) rs1234630372 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_223664,Human_RBP_ID_4073206,Human_RBP_ID_9270506,Human_RBP_ID_22428761 110808 RMVar_ID_110808 Human_SNP_ID_804574994 m1A Human chr1 + 2408825 2408825 2408825 GCACATGTATCCGCGATGGGTCCACCTGGATGATGCTGACGTACTCCTCCCCCAGGGTCTGGTAG GCACATGTATCCGCGATGGGTCCACCTGGATGTTGCTGACGTACTCCTCCCCCAGGGTCTGGTAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:2408776..2408885 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 3 stomach 110809 RMVar_ID_110809 Human_SNP_ID_804576086 m1A Human chr1 + 32770050 32770050 32770050 CGGAGGCGGAGGCTGGCGCTGAGACAGAGGCCATGCTGCAGCGCCACATTGACCGTGTCTACCGG CGGAGGCGGAGGCTGGCGCTGAGACAGAGGCCGTGCTGCAGCGCCACATTGACCGTGTCTACCGG A G KIAA1522 Ensembl:ENSG00000162522 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12730560 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,ESCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_27555332 GWAS_ID_11152,GWAS_ID_11153,GWAS_ID_11154,GWAS_ID_11155,GWAS_ID_11156,GWAS_ID_11157 110810 RMVar_ID_110810 Human_SNP_ID_804577324 m1A Human chr1 - 43452254 43452254 43452254 AGCTGATCGAATAGCAGTCAAGGCTGAGATGGAGGCCGTTTTTCTGGAGAACCTGAGGCATGCAG AGCTGATCGAATAGCAGTCAAGGCTGAGATGGTGGCCGTTTTTCTGGAGAACCTGAGGCATGCAG T A HYI Ensembl:ENSG00000178922 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43452195..43452445 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - Human_Splice_Rec_58356,Human_Splice_Rec_58357,Human_Splice_Rec_58372,Human_Splice_Rec_58373,Human_Splice_Rec_58388,Human_Splice_Rec_58389,Human_Splice_Rec_58404,Human_Splice_Rec_58405,Human_Splice_Rec_58416,Human_Splice_Rec_58417,Human_Splice_Rec_58428,Human_Splice_Rec_58429,Human_Splice_Rec_58442,Human_Splice_Rec_58443,Human_Splice_Rec_58456,Human_Splice_Rec_58457,Human_Splice_Rec_58467,Human_Splice_Rec_58480,Human_Splice_Rec_58481 RMVar_hsa_circ_341767 110811 RMVar_ID_110811 Human_SNP_ID_804586212 m1A Human chr1 - 212365067 212365067 212365067 GGGAGGAACAGCATGTAAAACTGGAACTTCTAACCCCGTCCCAAAAGAGGCGGTGTAGAGCCTAA GGGAGGAACAGCATGTAAAACTGGAACTTCTAGCCCCGTCCCAAAAGAGGCGGTGTAGAGCCTAA T C PACC1 Ensembl:ENSG00000065600 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:212365016..212365116 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_340680,Human_RBP_ID_27393637 RMVar_hsa_circ_139466,RMVar_hsa_circ_92209 110812 RMVar_ID_110812 Human_SNP_ID_804591749 m1A Human chr1 + 149886622 149886622 149886622 TTTCTTGGAGCCCTTTTTAGGGGCCGGAGCGGATTTTGCCGGTTCAGGCATGGTAAGACACAGTA TTTCTTGGAGCCCTTTTTAGGGGCCGGAGCGGTTTTTGCCGGTTCAGGCATGGTAAGACACAGTA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149886476..149886675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 110813 RMVar_ID_110813 Human_SNP_ID_804593955 m1A Human chr1 - 11681028 11681028 11681028 GCGGGAACCGAGCGCAGAGCCGGTACTGGGGGAGGGGAGAGGGGGCGGGATTCCCGCCGGGAGGG GCGGGAACCGAGCGCAGAGCCGGTACTGGGGGGGGGGAGAGGGGGCGGGATTCCCGCCGGGAGGG T C MAD2L2 Ensembl:ENSG00000116670 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:11681026..11681150 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5311525,Human_RBP_ID_8940110,Human_RBP_ID_19033905 110814 RMVar_ID_110814 Human_SNP_ID_804601183 m1A Human chr1 - 169106643 169106643 169106643 GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGAGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC GGAGGAGCCAAGGCAGGAGCAGGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGGCGGGGGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:169106326..169106802 26863196 MeRIP-seq:(Medium) rs1464228568 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110815 RMVar_ID_110815 Human_SNP_ID_804603892 m1A Human chr1 + 231020110 231020110 231020110 GGCTGTACAGTTGGCAGAGCAAGGACATGTCCAGCTGGCGGAGACCAACCTTGAGGGAAGGGGTG GGCTGTACAGTTGGCAGAGCAAGGACATGTCCTGCTGGCGGAGACCAACCTTGAGGGAAGGGGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:231020059..231020140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 110816 RMVar_ID_110816 Human_SNP_ID_804612450 m1A Human chr1 + 33277566 33277566 33277566 GAGTCTGGCTGCTAGGTGGAGACCCGGTTGTCAGGGGGTAAGCATGGAAGCAGGGAGACCTTCAG GAGTCTGGCTGCTAGGTGGAGACCCGGTTGTCGGGGGGTAAGCATGGAAGCAGGGAGACCTTCAG A G ZNF362 Ensembl:ENSG00000160094 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:33277564..33277766 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_66022,RMVar_hsa_circ_123326,RMVar_hsa_circ_131335,RMVar_hsa_circ_306184,RMVar_hsa_circ_125296,RMVar_hsa_circ_131341,RMVar_hsa_circ_131338,RMVar_hsa_circ_131339,RMVar_hsa_circ_307295,RMVar_hsa_circ_349056,RMVar_hsa_circ_327414 110817 RMVar_ID_110817 Human_SNP_ID_804628483 m1A Human chr1 - 29203187 29203187 29203187 CAGAATGCATCCAACAGCGGAGTGGGGCAAGCAGTCATCCAGATCGCCGCAGCCCTGGGCCTAAG CAGAATGCATCCAACAGCGGAGTGGGGCAAGCGGTCATCCAGATCGCCGCAGCCCTGGGCCTAAG T C MECR Ensembl:ENSG00000116353 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1062924 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 7 bladder,urinary tract Human_RBP_ID_849752,Human_RBP_ID_3935627 Human_Splice_Rec_39206,Human_Splice_Rec_39207,Human_Splice_Rec_39224,Human_Splice_Rec_39225,Human_Splice_Rec_39235,Human_Splice_Rec_39268,Human_Splice_Rec_39269,Human_Splice_Rec_39278,Human_Splice_Rec_39279,Human_Splice_Rec_39296,Human_Splice_Rec_39297,Human_Splice_Rec_39317,Human_Splice_Rec_39344,Human_Splice_Rec_39354 GWAS_ID_7756,GWAS_ID_7757,GWAS_ID_7758,GWAS_ID_7759,GWAS_ID_7760,GWAS_ID_7761,GWAS_ID_7762,GWAS_ID_7763,GWAS_ID_7764,GWAS_ID_7765,GWAS_ID_7766,GWAS_ID_7767,GWAS_ID_7768,GWAS_ID_7769,GWAS_ID_7770,GWAS_ID_7771,GWAS_ID_7772,GWAS_ID_7773,GWAS_ID_7774,GWAS_ID_7775,GWAS_ID_7776,GWAS_ID_7777,GWAS_ID_7778,GWAS_ID_7779,GWAS_ID_7780,GWAS_ID_7781,GWAS_ID_7782,GWAS_ID_7783,GWAS_ID_7784,GWAS_ID_7785,GWAS_ID_7786,GWAS_ID_7787,GWAS_ID_7788,GWAS_ID_7789,GWAS_ID_7790,GWAS_ID_7791,GWAS_ID_7792,GWAS_ID_7793,GWAS_ID_7794,GWAS_ID_7795,GWAS_ID_7796,GWAS_ID_7797,GWAS_ID_7798,GWAS_ID_7799,GWAS_ID_7800,GWAS_ID_7801,GWAS_ID_7802,GWAS_ID_7803,GWAS_ID_7804,GWAS_ID_7805,GWAS_ID_7806,GWAS_ID_7807,GWAS_ID_7808,GWAS_ID_7809,GWAS_ID_7810,GWAS_ID_7811,GWAS_ID_7812,GWAS_ID_7813,GWAS_ID_7814,GWAS_ID_7815,GWAS_ID_7816,GWAS_ID_7817,GWAS_ID_7818,GWAS_ID_7819,GWAS_ID_7820,GWAS_ID_7821,GWAS_ID_7822,GWAS_ID_7823,GWAS_ID_7824,GWAS_ID_7825,GWAS_ID_7826,GWAS_ID_7827,GWAS_ID_7828,GWAS_ID_7829,GWAS_ID_7830,GWAS_ID_7831,GWAS_ID_7832,GWAS_ID_7833,GWAS_ID_7834,GWAS_ID_7835,GWAS_ID_7836,GWAS_ID_7837,GWAS_ID_7838,GWAS_ID_7839,GWAS_ID_7840,GWAS_ID_7841,GWAS_ID_7842,GWAS_ID_7843,GWAS_ID_7844 RMVar_hsa_circ_26754,RMVar_hsa_circ_353558,RMVar_hsa_circ_17719,RMVar_hsa_circ_79279,RMVar_hsa_circ_6218,RMVar_hsa_circ_130945,RMVar_hsa_circ_318371,RMVar_hsa_circ_130947,RMVar_hsa_circ_370288,RMVar_hsa_circ_55808,RMVar_hsa_circ_130948 110818 RMVar_ID_110818 Human_SNP_ID_804629616 m1A Human chr1 - 1789054 1789054 1789054 AACGTCTGGGATGCACTCAAAGCCGACCGGGCAGGTACGTGGCCATGGGGCCTTTCTGTGTCTTG AACGTCTGGGATGCACTCAAAGCCGACCGGGCGGGTACGTGGCCATGGGGCCTTTCTGTGTCTTG T C GNB1 Ensembl:ENSG00000078369 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1789051..1789100 32194978 MeRIP-seq:(Medium) rs779971509 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_17223644,Human_RBP_ID_19033649,Human_RBP_ID_26797482 Human_Splice_Rec_6153,Human_Splice_Rec_6171,Human_Splice_Rec_6193 RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_98241,RMVar_hsa_circ_96576,RMVar_hsa_circ_128390,RMVar_hsa_circ_86973,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_128391,RMVar_hsa_circ_128388,RMVar_hsa_circ_128389,RMVar_hsa_circ_128397,RMVar_hsa_circ_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_376755,RMVar_hsa_circ_369314,RMVar_hsa_circ_94091,RMVar_hsa_circ_104378,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_128398,RMVar_hsa_circ_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_128396,RMVar_hsa_circ_320759,RMVar_hsa_circ_279629,RMVar_hsa_circ_89721,RMVar_hsa_circ_128401,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402 110819 RMVar_ID_110819 Human_SNP_ID_804632347 m1A Human chr1 + 120069545 120069545 120069545 TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGAAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC TTCAAAGGCTCAGGCCCTGGCGCTACGCTCCGCAGCCCAGGCGCAAATGCCTCGACTCCCCGCGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr1:120069399..120069625 26863196 MeRIP-seq:(Medium) rs587606395 Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 2 head and neck 110820 RMVar_ID_110820 Human_SNP_ID_804633926 m1A Human chr1 + 1627182 1627182 1627182 GGTGGCGCTGGGTAACGCAGCCCGGGCTCTGGACCTGCTGCGGAGGCGCCCAGAGCAGGCAAGCT GGTGGCGCTGGGTAACGCAGCCCGGGCTCTGGGCCTGCTGCGGAGGCGCCCAGAGCAGGCAAGCT A G MIB2 Ensembl:ENSG00000197530 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1626590..1627509 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 8 ovary Human_RBP_ID_223454,Human_RBP_ID_745793,Human_RBP_ID_851100,Human_RBP_ID_3934916,Human_RBP_ID_9269549,Human_RBP_ID_9355326,Human_RBP_ID_18964485,Human_RBP_ID_26310018 110821 RMVar_ID_110821 Human_SNP_ID_804654449 m1A Human chr1 - 115976613 115976613 115976613 CGCCTCCTCCACCTCCATGGCGGGCCGCGCGCAGGAACCCCGCCACCCCACCGCCCTCTCAGGCG CGCCTCCTCCACCTCCATGGCGGGCCGCGCGCGGGAACCCCGCCACCCCACCGCCCTCTCAGGCG T C LOC101928977,LOC101928977:2,LOC101928977:3,LOC101928977:4 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731,RNACentral:URS0000D5DBEE lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:115976564..115976666 26863196 MeRIP-seq:(Medium) rs1163423111 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 110822 RMVar_ID_110822 Human_SNP_ID_804656456 m1A Human chr1 + 205595282 205595282 205595282 CACGAATTACATGCTATTCCCTGATGGCACAAAAACTGTTCTGTACCTCCCTACTTTGGCACGTG CACGAATTACATGCTATTCCCTGATGGCACAAGAACTGTTCTGTACCTCCCTACTTTGGCACGTG A G MFSD4A Ensembl:ENSG00000174514 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:205595280..205595471 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver 110823 RMVar_ID_110823 Human_SNP_ID_804661437 m1A Human chr1 + 181049100 181049100 181049100 ATATTTTCGCCTGGGCGTTTCGGATCCCATCCATGGGGTCCCTGAATTTATTTCGGTTGGGTACG ATATTTTCGCCTGGGCGTTTCGGATCCCATCCTTGGGGTCCCTGAATTTATTTCGGTTGGGTACG A T MR1 Ensembl:ENSG00000153029 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_Splice_Rec_163184,Human_Splice_Rec_163194,Human_Splice_Rec_163206,Human_Splice_Rec_163212,Human_Splice_Rec_163214,Human_Splice_Rec_163224,Human_Splice_Rec_163232,Human_Splice_Rec_163244,Human_Splice_Rec_163252 RMVar_hsa_circ_73740,RMVar_hsa_circ_9771 110824 RMVar_ID_110824 Human_SNP_ID_804661440 m1A Human chr1 + 181049100 181049100 181049100 ATATTTTCGCCTGGGCGTTTCGGATCCCATCCATGGGGTCCCTGAATTTATTTCGGTTGGGTACG ATATTTTCGCCTGGGCGTTTCGGATCCCATCCGTGGGGTCCCTGAATTTATTTCGGTTGGGTACG A G MR1 Ensembl:ENSG00000153029 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2236410 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 17 stomach,haematopoietic and lymphoid tissue Human_Splice_Rec_163184,Human_Splice_Rec_163194,Human_Splice_Rec_163206,Human_Splice_Rec_163212,Human_Splice_Rec_163214,Human_Splice_Rec_163224,Human_Splice_Rec_163232,Human_Splice_Rec_163244,Human_Splice_Rec_163252 GWAS_ID_8382 RMVar_hsa_circ_73740,RMVar_hsa_circ_9771 110825 RMVar_ID_110825 Human_SNP_ID_804671446 m1A Human chr1 - 159920525 159920525 159920525 CGGGTGTGTCCTCTCCCTAGCTCCCCGCAGCCACCGCCACCCATTGGAATGGCCAACAGGGGACC CGGGTGTGTCCTCTCCCTAGCTCCCCGCAGCCCCCGCCACCCATTGGAATGGCCAACAGGGGACC T G TAGLN2 Ensembl:ENSG00000158710 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:159920475..159923473 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_222514,Human_RBP_ID_4074532,Human_RBP_ID_9319220 Human_Splice_Rec_146428,Human_Splice_Rec_146436,Human_Splice_Rec_146444,Human_Splice_Rec_146450,Human_Splice_Rec_146458 RMVar_hsa_circ_136988,RMVar_hsa_circ_113441,RMVar_hsa_circ_90034,RMVar_hsa_circ_136989,RMVar_hsa_circ_136990,RMVar_hsa_circ_378704,RMVar_hsa_circ_289074,RMVar_hsa_circ_118809,RMVar_hsa_circ_109388,RMVar_hsa_circ_323290,RMVar_hsa_circ_136991,RMVar_hsa_circ_136992 110826 RMVar_ID_110826 Human_SNP_ID_804673535 m1A Human chr1 + 231338544 231338544 231338544 GGACTTGCAGGCACTGTTTGTTCAGTTTAACGACCAATTCTTCTGGGGCCAGCTGGAGGCCGTCG GGACTTGCAGGCACTGTTTGTTCAGTTTAACGGCCAATTCTTCTGGGGCCAGCTGGAGGCCGTCG A G SPRTN Ensembl:ENSG00000010072 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:231338393..231338543 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_345786,Human_RBP_ID_1423831,Human_RBP_ID_22782781,Human_RBP_ID_26856729,Human_RBP_ID_27177986 Human_Splice_Rec_198381,Human_Splice_Rec_198387,Human_Splice_Rec_198391,Human_Splice_Rec_198399 110827 RMVar_ID_110827 Human_SNP_ID_804691815 m1A Human chr1 - 111619936 111619936 111619936 TGGGGCCGTCTGGAGCTCCCCGCCCCTTACTCACCCCCCCGGTCCGGCGCCTCCTCCACCTCCTC TGGGGCCGTCTGGAGCTCCCCGCCCCTTACTCCCCCCCCCGGTCCGGCGCCTCCTCCACCTCCTC T G LOC107985184-001 RNACentral:URS0000E60A45 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr1:111619859..111619999;chr1:111619844..111620006 26863410 MeRIP-seq:(Medium) rs1030124422 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110828 RMVar_ID_110828 Human_SNP_ID_804695975 m1A Human chr1 - 229625977 229625977 229625977 GGGCGCGGGGGCCCAGCTGAGCCGGCCGTCGGAGTGAGACCCTGCGGCAGAGACGACGGAGGCGG GGGCGCGGGGGCCCAGCTGAGCCGGCCGTCGGGGTGAGACCCTGCGGCAGAGACGACGGAGGCGG T C TAF5L Ensembl:ENSG00000135801 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:229625862..229626133 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_860414,Human_RBP_ID_9319443 Human_Splice_Rec_197355,Human_Splice_Rec_197363,Human_Splice_Rec_197369,Human_Splice_Rec_197377 RMVar_hsa_circ_114915,RMVar_hsa_circ_140339 110829 RMVar_ID_110829 Human_SNP_ID_804696055 m1A Human chr1 + 220253557 220253557 220253557 AGTCGGGGGTGGTGGGAGAAGGAGGAGGCGGCAAATCACTTATAAATGGCGCGGAAGCAGGACCC AGTCGGGGGTGGTGGGAGAAGGAGGAGGCGGCGAATCACTTATAAATGGCGCGGAAGCAGGACCC A G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879135241 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 110830 RMVar_ID_110830 Human_SNP_ID_804701658 m1A Human chr1 - 71080989 71080989 71080989 GGGTGGCTGTGCTGGTGGCGTTCAAGATGTCGACCAAGAATTTCCGAGTCAGTGACGGGGACTGG GGGTGGCTGTGCTGGTGGCGTTCAAGATGTCGTCCAAGAATTTCCGAGTCAGTGACGGGGACTGG T A ZRANB2 Ensembl:ENSG00000132485 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:71080880..71081050;chr1:71080874..71081005;chr1:71080863..71081025;chr1:71080885..71081025;chr1:71072101..71081025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_19778,Human_RBP_ID_742714,Human_RBP_ID_979753,Human_RBP_ID_1434892,Human_RBP_ID_1753692,Human_RBP_ID_3321399,Human_RBP_ID_4074127,Human_RBP_ID_5108664,Human_RBP_ID_8974239,Human_RBP_ID_11100422,Human_RBP_ID_24541163,Human_RBP_ID_26311453,Human_RBP_ID_26869227,Human_RBP_ID_27798219 Human_Splice_Rec_85643,Human_Splice_Rec_85663,Human_Splice_Rec_85693 RMVar_hsa_circ_82783,RMVar_hsa_circ_133922,RMVar_hsa_circ_133928,RMVar_hsa_circ_124017 110831 RMVar_ID_110831 Human_SNP_ID_804713128 m1A Human chr1 - 55056094 55056094 55056094 CAGCACGACCCCAGCCCTCGCCAGGCGCTGGCAGGCGGCGTTGAGGACGCGGCTGTACCCACCCG CAGCACGACCCCAGCCCTCGCCAGGCGCTGGCCGGCGGCGTTGAGGACGCGGCTGTACCCACCCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55056043..55056127 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 110832 RMVar_ID_110832 Human_SNP_ID_804744324 m1A Human chr1 - 226982084 226982084 226982084 CCGCACCACGCACCTTGCAGAGCGTGCGCACGATCCGCTCTGCATTGGCCTCGGACAGGAAAGGA CCGCACCACGCACCTTGCAGAGCGTGCGCACGTTCCGCTCTGCATTGGCCTCGGACAGGAAAGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:226982026..226982193 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 3 breast 110833 RMVar_ID_110833 Human_SNP_ID_804746723 m1A Human chr1 - 153943073 153943073 153943073 CCCAAGCCTGGCTTCCAAGTGCTTGACACGACACCCTACAGCCACTCAGCAAACCTGGCCCCTCC CCCAAGCCTGGCTTCCAAGTGCTTGACACGACGCCCTACAGCCACTCAGCAAACCTGGCCCCTCC T C DENND4B Ensembl:ENSG00000198837 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:153942951..153943154 26863196 MeRIP-seq:(Medium) rs754892693 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18187270,Human_RBP_ID_18552001 Human_Splice_Rec_132694,Human_Splice_Rec_132768,Human_Splice_Rec_132818 RMVar_hsa_circ_28451,RMVar_hsa_circ_124737,RMVar_hsa_circ_136323,RMVar_hsa_circ_99777,RMVar_hsa_circ_136337 110834 RMVar_ID_110834 Human_SNP_ID_804758119 m1A Human chr1 + 228635618 228635618 228635618 GCGCGCTCGCACGCGCGCGCGCGGACACACACACACACAGACACACACGCACACACGCACGCGCA GCGCGCTCGCACGCGCGCGCGCGGACACACACGCACACAGACACACACGCACACACGCACGCGCA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr1:228635551..228635650;chr1:228635576..228635650;chr1:228635513..228635701 26863196 MeRIP-seq:(Medium) rs199818102 Functional Loss SNV ICGC 33..33 33 SKCA 4 - 110835 RMVar_ID_110835 Human_SNP_ID_804761662 m1A Human chr1 - 236566007 236566007 236566007 ATTTTAGAAGCAGACACTGAATTTTGGTTTTCAGTCTGTTGTGAGTTTAGTGTCCAGCATCAGAT ATTTTAGAAGCAGACACTGAATTTTGGTTTTCGGTCTGTTGTGAGTTTAGTGTCCAGCATCAGAT T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:236564613..236566821 32194978 MeRIP-seq:(Medium) rs375051087 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_19053,Human_RBP_ID_1741708,Human_RBP_ID_3304432,Human_RBP_ID_18567897,Human_RBP_ID_23376561 Human_Splice_Rec_203312,Human_Splice_Rec_203313,Human_Splice_Rec_203398,Human_Splice_Rec_203399 RMVar_hsa_circ_275,RMVar_hsa_circ_4051,RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840,RMVar_hsa_circ_120373,RMVar_hsa_circ_17969,RMVar_hsa_circ_140845,RMVar_hsa_circ_21340,RMVar_hsa_circ_64336,RMVar_hsa_circ_140846,RMVar_hsa_circ_316425,RMVar_hsa_circ_336589,RMVar_hsa_circ_27638,RMVar_hsa_circ_4802 110836 RMVar_ID_110836 Human_SNP_ID_804765711 m1A Human chr1 - 110339999 110339999 110339999 CCCGACAGATGACTGATTTTCACACTTACATCACCGAAGCGTTTGAACTCATGAAACAGGCCGTC CCCGACAGATGACTGATTTTCACACTTACATCGCCGAAGCGTTTGAACTCATGAAACAGGCCGTC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:110339976..110340000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 5 lung 110837 RMVar_ID_110837 Human_SNP_ID_804771942 m1A Human chr1 + 156312148 156312148 156312148 AAAGTATTCATCTCCAATTTTCTTGATTTCCAACAGGCCTGCTCCTGTTCCAACATCATCTTCTC AAAGTATTCATCTCCAATTTTCTTGATTTCCATCAGGCCTGCTCCTGTTCCAACATCATCTTCTC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156312098..156312175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 110838 RMVar_ID_110838 Human_SNP_ID_804774234 m1A Human chr1 - 16643134 16643133 16643134 CAGGCTCTGTGTCTGCCTCAGCCTCCAGGACCACTGGCTGCCCATGAGAGACGAAGGATGGCATC CAGGCTCTGTGTCTGCCTCAGCCTCCAGGACC_CTGGCTGCCCATGAGAGACGAAGGATGGCATC GT G CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:16643035..16644685 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUAD 1 - Human_RBP_ID_849507,Human_RBP_ID_4072570,Human_RBP_ID_17730642,Human_RBP_ID_22871177 Human_Splice_Rec_22678,Human_Splice_Rec_22734,Human_Splice_Rec_22752 RMVar_hsa_circ_80199,RMVar_hsa_circ_11074,RMVar_hsa_circ_18591,RMVar_hsa_circ_129558,RMVar_hsa_circ_53215,RMVar_hsa_circ_316214 110839 RMVar_ID_110839 Human_SNP_ID_804775841 m1A Human chr1 - 220057933 220057933 220057933 GACATCGTGATCTGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACC GACATCGTGATCTGTCTGCCTCGGACTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGCACC T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878938199 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_341873 110840 RMVar_ID_110840 Human_SNP_ID_804785492 m1A Human chr1 - 155933786 155933786 155933786 GCCCCACTTCTCTTCCTCCCGCCAGCGGCCCCAGGTGGGGAGGTCACCAGCAGTGGGGGAAGTCC GCCCCACTTCTCTTCCTCCCGCCAGCGGCCCCCGGTGGGGAGGTCACCAGCAGTGGGGGAAGTCC T G KHDC4 Ensembl:ENSG00000132680 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:155933740..155933870 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_19837,Human_RBP_ID_221878,Human_RBP_ID_273346,Human_RBP_ID_18415647,Human_RBP_ID_18969095,Human_RBP_ID_23206138 Human_Splice_Rec_140582,Human_Splice_Rec_140606,Human_Splice_Rec_140654,Human_Splice_Rec_140672,Human_Splice_Rec_140690,Human_Splice_Rec_140700 RMVar_hsa_circ_117053,RMVar_hsa_circ_136725,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_62977 110841 RMVar_ID_110841 Human_SNP_ID_804787367 m1A Human chr1 + 110340216 110340216 110340216 CTTTAGACAAAGATACTTATCCTCCATCAGCCAGTGTGGTCGGGGCCTCTGTAGGTGGTCACCGG CTTTAGACAAAGATACTTATCCTCCATCAGCCGGTGTGGTCGGGGCCTCTGTAGGTGGTCACCGG A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:110340176..110340300 26863196 MeRIP-seq:(Medium) rs769664209 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_1407921,Human_RBP_ID_5519107,Human_RBP_ID_8280560,Human_RBP_ID_8732376,Human_RBP_ID_9252956,Human_RBP_ID_22014750,Human_RBP_ID_22124406,Human_RBP_ID_26837089,Human_RBP_ID_27164733 110842 RMVar_ID_110842 Human_SNP_ID_804791682 m1A Human chr1 + 42697242 42697242 42697242 GGTAGACCAGTGAGGCAGAATATGTATCGGGGATATAGACCACGATTCCGCAGGTATGGTCCACG GGTAGACCAGTGAGGCAGAATATGTATCGGGGCTATAGACCACGATTCCGCAGGTATGGTCCACG A C YBX1 Ensembl:ENSG00000065978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:42697226..42697275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_24699407 Human_Splice_Rec_56422,Human_Splice_Rec_56423,Human_Splice_Rec_56434,Human_Splice_Rec_56442,Human_Splice_Rec_56443,Human_Splice_Rec_56454 RMVar_hsa_circ_58394,RMVar_hsa_circ_118671,RMVar_hsa_circ_132186,RMVar_hsa_circ_71356,RMVar_hsa_circ_300896,RMVar_hsa_circ_132190,RMVar_hsa_circ_118994,RMVar_hsa_circ_124394,RMVar_hsa_circ_132192 110843 RMVar_ID_110843 Human_SNP_ID_804803229 m1A Human chr1 + 44645460 44645460 44645460 ATGGTGAAAGCAGCAAGCAGGAGGCCATGCAGAAGACCTGCAAGAACAGCGACATCGAGAAGTAA ATGGTGAAAGCAGCAAGCAGGAGGCCATGCAGGAGACCTGCAAGAACAGCGACATCGAGAAGTAA A G RNF220 Ensembl:ENSG00000187147 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:44645401..44645475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 8 liver Human_RBP_ID_9358772,Human_RBP_ID_18968241,Human_RBP_ID_22350441,Human_RBP_ID_26314112 Human_Splice_Rec_61526,Human_Splice_Rec_61527,Human_Splice_Rec_61552,Human_Splice_Rec_61553,Human_Splice_Rec_61576,Human_Splice_Rec_61577,Human_Splice_Rec_61610,Human_Splice_Rec_61611,Human_Splice_Rec_61624,Human_Splice_Rec_61625,Human_Splice_Rec_61640,Human_Splice_Rec_61641,Human_Splice_Rec_61678,Human_Splice_Rec_61679,Human_Splice_Rec_61694,Human_Splice_Rec_61695,Human_Splice_Rec_61704,Human_Splice_Rec_61705,Human_Splice_Rec_61714,Human_Splice_Rec_61715 RMVar_hsa_circ_14630,RMVar_hsa_circ_62880,RMVar_hsa_circ_18314 110844 RMVar_ID_110844 Human_SNP_ID_804857315 m1A Human chr1 - 205720577 205720577 205720577 CAACGGCAGGCGGCATCTAAAGCAGCTTCTAAACAGAGAGAGATGCTCATGGAAGATGTGGGCAG CAACGGCAGGCGGCATCTAAAGCAGCTTCTAATCAGAGAGAGATGCTCATGGAAGATGTGGGCAG T A NUCKS1 Ensembl:ENSG00000069275 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:205720526..205720625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_RBP_ID_221145,Human_RBP_ID_339192,Human_RBP_ID_801127,Human_RBP_ID_974285,Human_RBP_ID_1438352,Human_RBP_ID_1734000,Human_RBP_ID_4087700,Human_RBP_ID_5744151,Human_RBP_ID_9357428,Human_RBP_ID_17449032,Human_RBP_ID_17736429,Human_RBP_ID_18222802,Human_RBP_ID_18429333,Human_RBP_ID_22026532,Human_RBP_ID_22871881,Human_RBP_ID_23424777,Human_RBP_ID_24541341,Human_RBP_ID_26312579,Human_RBP_ID_27585366,Human_RBP_ID_27799162 Human_Splice_Rec_179900,Human_Splice_Rec_179901 RMVar_hsa_circ_100041,RMVar_hsa_circ_67551,RMVar_hsa_circ_373543,RMVar_hsa_circ_347275,RMVar_hsa_circ_139227,RMVar_hsa_circ_109624,RMVar_hsa_circ_139228,RMVar_hsa_circ_139229 110845 RMVar_ID_110845 Human_SNP_ID_804858329 m1A Human chr1 - 156671350 156671350 156671350 GAGGAGGAGGGACAGGAGCTGCCGCAGTCTGCAGATGTGCAGAGGTGGGAAGATACGGTGGAGAA GAGGAGGAGGGACAGGAGCTGCCGCAGTCTGCTGATGTGCAGAGGTGGGAAGATACGGTGGAGAA T A NES Ensembl:ENSG00000132688 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:156671251..156671390 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_22871863,Human_RBP_ID_23117574 RMVar_hsa_circ_136883,RMVar_hsa_circ_113100,RMVar_hsa_circ_122426,RMVar_hsa_circ_85602,RMVar_hsa_circ_136884,RMVar_hsa_circ_136882 110846 RMVar_ID_110846 Human_SNP_ID_804865626 m1A Human chr1 - 207044014 207044014 207044014 TTTGCCTATTTGCCAGCATTTTTTGAAGTAATACACTGCTGCTACCTGGAAGATGTCTAACTTCA TTTGCCTATTTGCCAGCATTTTTTGAAGTAATGCACTGCTGCTACCTGGAAGATGTCTAACTTCA T C YOD1 Ensembl:ENSG00000180667 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044145 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 3 oesophagus Human_RBP_ID_339451,Human_RBP_ID_5745232,Human_RBP_ID_23358982 Human_miRNA_ID_1740664,Human_miRNA_ID_2097677,Human_miRNA_ID_2103620,Human_miRNA_ID_2109575,Human_miRNA_ID_2162123,Human_miRNA_ID_2593329,Human_miRNA_ID_2649035,Human_miRNA_ID_2650981,Human_miRNA_ID_2736291,Human_miRNA_ID_3036890 GWAS_ID_9207,GWAS_ID_9208,GWAS_ID_9209,GWAS_ID_9210,GWAS_ID_9211 RMVar_hsa_circ_76858,RMVar_hsa_circ_98794,RMVar_hsa_circ_119330,RMVar_hsa_circ_82638,RMVar_hsa_circ_139272,RMVar_hsa_circ_139273,RMVar_hsa_circ_139274,RMVar_hsa_circ_139271 110847 RMVar_ID_110847 Human_SNP_ID_804865734 m1A Human chr1 + 11658828 11658828 11658828 CGCGCACGCGCCTCTGGGGACCTTCCAGCCAGACCCGGCGACCATCCAGCAGAAGAGCGATGCCA CGCGCACGCGCCTCTGGGGACCTTCCAGCCAGGCCCGGCGACCATCCAGCAGAAGAGCGATGCCA A G FBXO44 Ensembl:ENSG00000132879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11658779..11658850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_9358075,Human_RBP_ID_24747917 Human_Splice_Rec_17346,Human_Splice_Rec_17347,Human_Splice_Rec_17356,Human_Splice_Rec_17366,Human_Splice_Rec_17367,Human_Splice_Rec_17376,Human_Splice_Rec_17377,Human_Splice_Rec_17386,Human_Splice_Rec_17387,Human_Splice_Rec_17396,Human_Splice_Rec_17397,Human_Splice_Rec_17404,Human_Splice_Rec_17405,Human_Splice_Rec_17410,Human_Splice_Rec_17411,Human_Splice_Rec_17416,Human_Splice_Rec_17417 RMVar_hsa_circ_129170,RMVar_hsa_circ_312251,RMVar_hsa_circ_70464 110848 RMVar_ID_110848 Human_SNP_ID_804883802 m1A Human chr1 - 3469503 3469503 3469503 GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCAGGAACTCCTCCACCAGGATGCTCAGGCTGTGC GGGTCACGGTCGCCCGCAGCTCCTTGGACTGCCGGAACTCCTCCACCAGGATGCTCAGGCTGTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:3468931..3469527 32194978 MeRIP-seq:(Medium) rs553627615 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 9 head and neck 110849 RMVar_ID_110849 Human_SNP_ID_804911570 m1A Human chr1 + 178093801 178093801 178093801 CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCACCGCCACCGCCACCGCCGTGGCTGCC CCGCTGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCACCGCCACCGCCACCGCCGTGGCTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:178093752..178094213 26863196 MeRIP-seq:(Medium) rs557601483 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 110850 RMVar_ID_110850 Human_SNP_ID_804921609 m1A Human chr1 + 32231122 32231122 32231122 CTGGTGCCTGGCTATCTTTTTCCAGCTACAGCAGCGGCGGCGAAGATGGTTACGTCCGTATCCAT CTGGTGCCTGGCTATCTTTTTCCAGCTACAGCGGCGGCGGCGAAGATGGTTACGTCCGTATCCAT A G EIF3I Ensembl:ENSG00000084623 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:32231101..32231225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_741710,Human_RBP_ID_859217,Human_RBP_ID_4094267,Human_RBP_ID_8968955 Human_Splice_Rec_43016 RMVar_hsa_circ_84932,RMVar_hsa_circ_131200,RMVar_hsa_circ_83976,RMVar_hsa_circ_131214,RMVar_hsa_circ_131223,RMVar_hsa_circ_97501,RMVar_hsa_circ_117717,RMVar_hsa_circ_131220,RMVar_hsa_circ_131222,RMVar_hsa_circ_108423 110851 RMVar_ID_110851 Human_SNP_ID_804926242 m1A Human chr1 + 46278837 46278837 46278837 CATGCTTCAGCCCCTGCAAGCTGATGGTACCGAGCATGAGACTGTGAGGTACGGGCCCCATCACA CATGCTTCAGCCCCTGCAAGCTGATGGTACCGGGCATGAGACTGTGAGGTACGGGCCCCATCACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:46278511..46279025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_11011157,Human_RBP_ID_22785261 110852 RMVar_ID_110852 Human_SNP_ID_804937910 m1A Human chr1 + 46363028 46363028 46363028 TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTATATAATTTTAGAATACCTGAAGGCTTCTTGGC TTTCCTGGAAAACATCCTGTGCAGAAAAGGGTGTATAATTTTAGAATACCTGAAGGCTTCTTGGC A G NSUN4 Ensembl:ENSG00000117481 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17361833 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_11012630,Human_RBP_ID_19373009,Human_RBP_ID_26386039,Human_RBP_ID_27595369 GWAS_ID_13371,GWAS_ID_13372,GWAS_ID_13373,GWAS_ID_13374 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649 110853 RMVar_ID_110853 Human_SNP_ID_804958473 m1A Human chr1 - 112849937 112849937 112849937 GTGGCGGCGACGCTCCCGGGAGACGCGGGGGGAGAACCAGTCTGTGCGCGCGGCTGTGAGAAGCC GTGGCGGCGACGCTCCCGGGAGACGCGGGGGGGGAACCAGTCTGTGCGCGCGGCTGTGAGAAGCC T C LINC01356 Ensembl:ENSG00000215866 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:112849889..112849985 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110854 RMVar_ID_110854 Human_SNP_ID_804971439 m1A Human chr1 - 109494172 109494172 109494172 AGCCAGCGGGTCAGTCTCGGCTCCCCAGCTGGAGCGGGAACCAGACCTACCTCCAGGGGCTGCAT AGCCAGCGGGTCAGTCTCGGCTCCCCAGCTGGGGCGGGAACCAGACCTACCTCCAGGGGCTGCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:109494126..109494230 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 9 head and neck 110855 RMVar_ID_110855 Human_SNP_ID_804971577 m1A Human chr1 - 168085608 168085608 168085608 TCCCGGGGGGCGGCTTCGGGGGCCGCCGAGGCAGCAGAACTCTTGTGAGCCAGAGGCTGCAGTTG TCCCGGGGGGCGGCTTCGGGGGCCGCCGAGGCGGCAGAACTCTTGTGAGCCAGAGGCTGCAGTTG T C GPR161 Ensembl:ENSG00000143147 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:168085559..168085652 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach Human_RBP_ID_332079 RMVar_hsa_circ_137398,RMVar_hsa_circ_137399 110856 RMVar_ID_110856 Human_SNP_ID_804979458 m1A Human chr1 - 151874373 151874373 151874373 AAGAACCCATCTCAAACAAACAAACAAACAAAAAAAAAAAACTCTTGTCTCCTTAGGATATGTTA AAGAACCCATCTCAAACAAACAAACAAACAAACAAAAAAAACTCTTGTCTCCTTAGGATATGTTA T G THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3180671 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_27388283 Human_miRNA_ID_179613 110857 RMVar_ID_110857 Human_SNP_ID_804990251 m1A Human chr1 - 112703799 112703799 112703799 ATCCCCAATACGTCTTTCCTGGCAGCCCCACCATGGCTGCAATCCGAAAGAAGCTGGTGATCGTT ATCCCCAATACGTCTTTCCTGGCAGCCCCACCCTGGCTGCAATCCGAAAGAAGCTGGTGATCGTT T G RHOC,AL603832.3 Ensembl:ENSG00000155366,Ensembl:ENSG00000271810 Protein coding,Protein coding start codon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:112703613..112710468 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 10 brain Human_RBP_ID_851673,Human_RBP_ID_3982995,Human_RBP_ID_5109174,Human_RBP_ID_5312641,Human_RBP_ID_18187212,Human_RBP_ID_24541688,Human_RBP_ID_24573432 Human_Splice_Rec_110608,Human_Splice_Rec_110618,Human_Splice_Rec_110626,Human_Splice_Rec_110636,Human_Splice_Rec_110646,Human_Splice_Rec_110658,Human_Splice_Rec_110668,Human_Splice_Rec_110676,Human_Splice_Rec_110688,Human_Splice_Rec_110700,Human_Splice_Rec_110710,Human_Splice_Rec_110718,Human_Splice_Rec_110728,Human_Splice_Rec_110734,Human_Splice_Rec_110746,Human_Splice_Rec_110752,Human_Splice_Rec_110758,Human_Splice_Rec_110766,Human_Splice_Rec_110776,Human_Splice_Rec_110790,Human_Splice_Rec_110802,Human_Splice_Rec_110812 RMVar_hsa_circ_80904,RMVar_hsa_circ_8503,RMVar_hsa_circ_110082,RMVar_hsa_circ_112194,RMVar_hsa_circ_135387,RMVar_hsa_circ_104408,RMVar_hsa_circ_84742,RMVar_hsa_circ_135385,RMVar_hsa_circ_135386,RMVar_hsa_circ_135384,RMVar_hsa_circ_54846,RMVar_hsa_circ_101563,RMVar_hsa_circ_84521,RMVar_hsa_circ_104091,RMVar_hsa_circ_135393,RMVar_hsa_circ_135394,RMVar_hsa_circ_90166,RMVar_hsa_circ_135396,RMVar_hsa_circ_135397,RMVar_hsa_circ_135395 110858 RMVar_ID_110858 Human_SNP_ID_804990579 m1A Human chr1 + 33036767 33036767 33036767 CCTGGGTCCCTTTACCGGCCCCGGGAGGCCCCAGCAGCACGGCCCGGATGCCTTTAGGATACTCG CCTGGGTCCCTTTACCGGCCCCGGGAGGCCCCGGCAGCACGGCCCGGATGCCTTTAGGATACTCG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:33036726..33036850 26863410 MeRIP-seq:(Medium) rs915278688 Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 8 lung 110859 RMVar_ID_110859 Human_SNP_ID_804996978 m1A Human chr1 - 116517648 116517648 116517648 GAGGCGGGACTGGGGAAGCAAAGTCCAGGATCAGAGCCAGGGTAGCCCCGGGTTAGAGACTCGAG GAGGCGGGACTGGGGAAGCAAAGTCCAGGATCTGAGCCAGGGTAGCCCCGGGTTAGAGACTCGAG T A CD58 Ensembl:ENSG00000116815 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116516993..116517797 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_127652,RMVar_hsa_circ_135629 110860 RMVar_ID_110860 Human_SNP_ID_804998861 m1A Human chr1 + 244835731 244835731 244835731 TCGCGGAGTAGTCCTCATGGCCGCCCCGCCGGAGCCCGGTGAGCCCGAGGAGAGGAAGGTAACCT TCGCGGAGTAGTCCTCATGGCCGCCCCGCCGGGGCCCGGTGAGCCCGAGGAGAGGAAGGTAACCT A G COX20 Ensembl:ENSG00000203667 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:244835697..244835908 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_976856,Human_RBP_ID_4074894,Human_RBP_ID_5339033,Human_RBP_ID_22427895,Human_RBP_ID_22871666,Human_RBP_ID_23380147 Human_Splice_Rec_207183,Human_Splice_Rec_207191,Human_Splice_Rec_207195,Human_Splice_Rec_207201 110861 RMVar_ID_110861 Human_SNP_ID_804999017 m1A Human chr1 - 247329538 247329538 247329538 AGCCCTGTGCCCCCGAGTCTTGGCTCCGAAGGAAAGTGAGGAGCCCAGGAAAATGAGGAGCCCAC AGCCCTGTGCCCCCGAGTCTTGGCTCCGAAGGCAAGTGAGGAGCCCAGGAAAATGAGGAGCCCAC T G ZNF496 Ensembl:ENSG00000162714 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:247329487..247329553 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_851036,Human_RBP_ID_9357768 Human_Splice_Rec_208726,Human_Splice_Rec_208758,Human_Splice_Rec_208766 RMVar_hsa_circ_73657,RMVar_hsa_circ_351460 110862 RMVar_ID_110862 Human_SNP_ID_805000417 m1A Human chr1 + 53940060 53940060 53940060 TAGCTAAAATCACTTCGGACCCTTCAGAGCTCAGACAGAGATCAATTTTTCTCATCTTAAAGTGT TAGCTAAAATCACTTCGGACCCTTCAGAGCTCTGACAGAGATCAATTTTTCTCATCTTAAAGTGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:53940001..53940100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 6 kidney 110863 RMVar_ID_110863 Human_SNP_ID_805004711 m1A Human chr1 - 23318572 23318572 23318572 ACAAGTCAGCAGCACAAGCCAGACGCCGGCTGATGAGTGGAAAAGTAAAAGTGTGGGGAAATGTA ACAAGTCAGCAGCACAAGCCAGACGCCGGCTGGTGAGTGGAAAAGTAAAAGTGTGGGGAAATGTA T C HNRNPR Ensembl:ENSG00000125944 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23318522..23318600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 6 oesophagus Human_RBP_ID_347539,Human_RBP_ID_3304251,Human_RBP_ID_9355680,Human_RBP_ID_10859079,Human_RBP_ID_22783069,Human_RBP_ID_23376364,Human_RBP_ID_26310477,Human_RBP_ID_26857802,Human_RBP_ID_27797540 Human_Splice_Rec_29761,Human_Splice_Rec_29777,Human_Splice_Rec_29795,Human_Splice_Rec_29819,Human_Splice_Rec_29835,Human_Splice_Rec_29851,Human_Splice_Rec_29865,Human_Splice_Rec_29871 RMVar_hsa_circ_67146,RMVar_hsa_circ_61314,RMVar_hsa_circ_55947,RMVar_hsa_circ_55437,RMVar_hsa_circ_57520,RMVar_hsa_circ_356207 110864 RMVar_ID_110864 Human_SNP_ID_805007757 m1A Human chr1 + 161366317 161366316 161366317 TACAAGTGGGAGAGATAAAGGTTTGTGAGGGGAAAAAGGGAAGTATTTGGGGAGCTTGGTCAGAG TACAAGTGGGAGAGATAAAGGTTTGTGAGGGG_AAAAGGGAAGTATTTGGGGAGCTTGGTCAGAG GA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:161366227..161366418 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_5700698,Human_RBP_ID_18218212 110865 RMVar_ID_110865 Human_SNP_ID_805012196 m1A Human chr1 + 16608775 16608775 16608775 TTCGCCTGGGTCTAAACAGGATTTGCCTTCAGATTGCCTGTGAGATAAAAGAGAGAAATCAAGGT TTCGCCTGGGTCTAAACAGGATTTGCCTTCAGGTTGCCTGTGAGATAAAAGAGAGAAATCAAGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16608701..16608820 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 110866 RMVar_ID_110866 Human_SNP_ID_805013117 m1A Human chr1 + 160092604 160092604 160092604 CAGCTGGCGGCCAGCCGCAGTCCTGGGGGGCCACCCCGCACAGAGATGTTGCACAGCAGGGAGGC CAGCTGGCGGCCAGCCGCAGTCCTGGGGGGCCGCCCCGCACAGAGATGTTGCACAGCAGGGAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:160091864..160094010 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 110867 RMVar_ID_110867 Human_SNP_ID_805018209 m1A Human chr1 + 31653958 31653958 31653958 GACCCTGGAGCACCTGGCCTGCCCGGAGCACCATCCTTCCCTGGAGGCCCTGGTCGTCCCGGAGC GACCCTGGAGCACCTGGCCTGCCCGGAGCACCGTCCTTCCCTGGAGGCCCTGGTCGTCCCGGAGC A G PEF1-AS1 Ensembl:ENSG00000235790 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:31653910..31654042 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110868 RMVar_ID_110868 Human_SNP_ID_805018718 m1A Human chr1 - 151524771 151524771 151524771 GGGAGGCTACCTCCTCTTTCAGGGCCCCCTTCAGGGCTGTCAACTCCCGCTCCCGCAGCCTCAGC GGGAGGCTACCTCCTCTTTCAGGGCCCCCTTCGGGGCTGTCAACTCCCGCTCCCGCAGCCTCAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:151524722..151524842 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110869 RMVar_ID_110869 Human_SNP_ID_805022055 m1A Human chr1 + 16149047 16149047 16149047 CATGTCATTCATGATGTTCTGCATCAGGTCCCACTGTGGGGGGAAGATACAGGTTAGTGTGGGCA CATGTCATTCATGATGTTCTGCATCAGGTCCCCCTGTGGGGGGAAGATACAGGTTAGTGTGGGCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16148783..16149080 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 2 head and neck 110870 RMVar_ID_110870 Human_SNP_ID_805033359 m1A Human chr1 + 54887052 54887052 54887052 ACACCCAGCGCTGGTGGATGAGCACGAACTCCAGCCCCTTCAGGCGCACCCACAGCAGGAAGAGC ACACCCAGCGCTGGTGGATGAGCACGAACTCCTGCCCCTTCAGGCGCACCCACAGCAGGAAGAGC A T AC096536.2 Ensembl:ENSG00000242396 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:54887001..54887114 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_75093 110871 RMVar_ID_110871 Human_SNP_ID_805040989 m1A Human chr1 - 151033891 151033891 151033891 GTTTCTTTCGAGAGACCTGGGTGTTGCCTTGAAGATAGGCATGGAGGTTAGGGTGGGTACTTGAG GTTTCTTTCGAGAGACCTGGGTGTTGCCTTGACGATAGGCATGGAGGTTAGGGTGGGTACTTGAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:151033841..151033929 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 110872 RMVar_ID_110872 Human_SNP_ID_805056068 m1A Human chr1 - 153747072 153747072 153747072 TGAGCTGGATCTTGTCTTTTCTTTCTGGCCTTACCTGAGTACGGCAGGTATCCTGCAGCTTCAGG TGAGCTGGATCTTGTCTTTTCTTTCTGGCCTTGCCTGAGTACGGCAGGTATCCTGCAGCTTCAGG T C AL513523.6 Ensembl:ENSG00000243613 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153747070..153747171 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 110873 RMVar_ID_110873 Human_SNP_ID_805059961 m1A Human chr1 + 23019847 23019847 23019847 CCTGGCGGAACCGCCGGGGTCCGCAGGGCCTCAGGCCGGCCCTACTGTCGTGCCTGGGTCTGCGA CCTGGCGGAACCGCCGGGGTCCGCAGGGCCTCGGGCCGGCCCTACTGTCGTGCCTGGGTCTGCGA A G KDM1A Ensembl:ENSG00000004487 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:23019746..23019897 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_4075256,Human_RBP_ID_5312371,Human_RBP_ID_8302617,Human_RBP_ID_8753744,Human_RBP_ID_9269945,Human_RBP_ID_9318694,Human_RBP_ID_18415794,Human_RBP_ID_18566745,Human_RBP_ID_22428206 Human_miRNA_ID_2008334 RMVar_hsa_circ_130376,RMVar_hsa_circ_84363,RMVar_hsa_circ_122955,RMVar_hsa_circ_130377 110874 RMVar_ID_110874 Human_SNP_ID_805066231 m1A Human chr1 + 22091494 22091494 22091494 TGGCTGCCCTGGAGCCTCCAGAACCGAAGAAGAGCCGCAGGTGTGTGCTGCTATGAACATCTCTC TGGCTGCCCTGGAGCCTCCAGAACCGAAGAAGTGCCGCAGGTGTGTGCTGCTATGAACATCTCTC A T CDC42 Ensembl:ENSG00000070831 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_342776,Human_RBP_ID_1421606,Human_RBP_ID_5762151,Human_RBP_ID_10790508 Human_Splice_Rec_29062,Human_Splice_Rec_29072,Human_Splice_Rec_29084,Human_Splice_Rec_29116,Human_Splice_Rec_29164 Human_miRNA_ID_941748,Human_miRNA_ID_1049691,Human_miRNA_ID_2097261,Human_miRNA_ID_2103204,Human_miRNA_ID_2109165,Human_miRNA_ID_2161710,Human_miRNA_ID_2427989,Human_miRNA_ID_2487787,Human_miRNA_ID_2592914,Human_miRNA_ID_2648882,Human_miRNA_ID_2735876,Human_miRNA_ID_3036479 RMVar_hsa_circ_97695,RMVar_hsa_circ_378086,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_95831,RMVar_hsa_circ_105385,RMVar_hsa_circ_130362,RMVar_hsa_circ_130364,RMVar_hsa_circ_130365 110875 RMVar_ID_110875 Human_SNP_ID_805068182 m1A Human chr1 + 220768619 220768619 220768619 TCAGGTCATTTGGCAAACCTGTATAGGGCCCCAGTCACTGTGGATGGGCTGGGGGGTCATGGGTG TCAGGTCATTTGGCAAACCTGTATAGGGCCCCGGTCACTGTGGATGGGCTGGGGGGTCATGGGTG A G MTARC2 Ensembl:ENSG00000117791 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:220768613..220768717 26863196 MeRIP-seq:(Medium) rs75742660 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_139749,RMVar_hsa_circ_338300,RMVar_hsa_circ_139751 110876 RMVar_ID_110876 Human_SNP_ID_805071346 m1A Human chr1 - 55052747 55052747 55052747 CGCTAACCGTGCCCTTCCCTTGGCAGTTGAGCACGCGCAGGCTGCGCATGCTGGCACCCTTGGCC CGCTAACCGTGCCCTTCCCTTGGCAGTTGAGCGCGCGCAGGCTGCGCATGCTGGCACCCTTGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:55052697..55052807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 110877 RMVar_ID_110877 Human_SNP_ID_805073618 m1A Human chr1 + 41241439 41241439 41241439 GCACTGGGGCAGGCGGCACACGTGAGTCGGCCAGCCGGGGCCCAGCCCCCAGGACGCTGCTGACA GCACTGGGGCAGGCGGCACACGTGAGTCGGCCGGCCGGGGCCCAGCCCCCAGGACGCTGCTGACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:41241431..41241515 26863196 MeRIP-seq:(Medium) rs12125555 Functional Loss SNV ICGC 33..33 33 LAML 1 - 110878 RMVar_ID_110878 Human_SNP_ID_805076648 m1A Human chr1 + 152032647 152032647 152032647 GGCTGGAAGGAAAGGGGGTGGGTTTGAAGGCCAGGGCCAAGGGGTCCTCAGGTCCGCTTCTGGGA GGCTGGAAGGAAAGGGGGTGGGTTTGAAGGCCTGGGCCAAGGGGTCCTCAGGTCCGCTTCTGGGA A T AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T cell line,total RNA;HTR8/Svneo,Hypoxia IP chr1:152032601..152032714;chr1:152032601..152032800 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 2 kidney 110879 RMVar_ID_110879 Human_SNP_ID_805084425 m1A Human chr1 + 156744961 156744961 156744961 TCATCTGTGGGCCGGGGGCTGCCAGAGCCCACAGCCACATCTGCTTTCCAGGGGGTCTCTGGGGC TCATCTGTGGGCCGGGGGCTGCCAGAGCCCACCGCCACATCTGCTTTCCAGGGGGTCTCTGGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:156744958..156745188 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus 110880 RMVar_ID_110880 Human_SNP_ID_805098111 m1A Human chr1 + 155688196 155688196 155688196 CCTCCCGCTTGTCAGGAGGCGGCCAGCGGGTAAGCCGACTGGCGGAAATGCGAGAGAGGAGAAGG CCTCCCGCTTGTCAGGAGGCGGCCAGCGGGTACGCCGACTGGCGGAAATGCGAGAGAGGAGAAGG A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:155688145..155688294 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110881 RMVar_ID_110881 Human_SNP_ID_805107184 m1A Human chr1 + 36301001 36301001 36301001 CTGAAGAGACAGAGGAAAGAGAGGAGAGCACCACGGGCTTTGACAAATCAAGACTGGGGACCAAA CTGAAGAGACAGAGGAAAGAGAGGAGAGCACCGCGGGCTTTGACAAATCAAGACTGGGGACCAAA A G THRAP3 Ensembl:ENSG00000054118 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:36300953..36301122 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_17008,Human_RBP_ID_978016,Human_RBP_ID_1430739,Human_RBP_ID_1747072,Human_RBP_ID_2145851,Human_RBP_ID_5156100,Human_RBP_ID_5819162,Human_RBP_ID_8310085,Human_RBP_ID_8748719,Human_RBP_ID_9270064,Human_RBP_ID_9356038,Human_RBP_ID_10968072,Human_RBP_ID_17452840,Human_RBP_ID_18573814,Human_RBP_ID_22784849,Human_RBP_ID_24541084,Human_RBP_ID_26309724,Human_RBP_ID_27182525,Human_RBP_ID_27797821 Human_Splice_Rec_47691,Human_Splice_Rec_47713,Human_Splice_Rec_47735 Human_miRNA_ID_656545 RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673,RMVar_hsa_circ_127926,RMVar_hsa_circ_111248,RMVar_hsa_circ_131676,RMVar_hsa_circ_71646,RMVar_hsa_circ_131677,RMVar_hsa_circ_54612,RMVar_hsa_circ_369463,RMVar_hsa_circ_131682,RMVar_hsa_circ_69610,RMVar_hsa_circ_84472,RMVar_hsa_circ_120693,RMVar_hsa_circ_131683,RMVar_hsa_circ_116242,RMVar_hsa_circ_131684,RMVar_hsa_circ_80250,RMVar_hsa_circ_131685,RMVar_hsa_circ_365466,RMVar_hsa_circ_131686 110882 RMVar_ID_110882 Human_SNP_ID_805108372 m1A Human chr1 + 228321558 228321558 228321558 GGAAGGGCCCATGTTCTCCCACACATTTGGGGACACCGAGGCACAGGTGGGGGATGCCCTGCGGC GGAAGGGCCCATGTTCTCCCACACATTTGGGGGCACCGAGGCACAGGTGGGGGATGCCCTGCGGC A G OBSCN Ensembl:ENSG00000154358 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228321507..228321624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus RMVar_hsa_circ_268044,RMVar_hsa_circ_267468,RMVar_hsa_circ_268744,RMVar_hsa_circ_100633,RMVar_hsa_circ_140242 110883 RMVar_ID_110883 Human_SNP_ID_805111172 m1A Human chr1 - 1605668 1605648 1605669 CCTGACCAGCCCAGCCCACACCTGACCAGCCGACCCCACACCTGACCAGCCCAGCCCAGCCCACA CCTGACCAGCCCAGCCCACACCTGACCAGCC_____________________AGCCCAGCCCACA TGGGCTGGTCAGGTGTGGGGTC T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:1605664..1605798 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..52 33 SKCA 4 - 110884 RMVar_ID_110884 Human_SNP_ID_805132129 m1A Human chr1 + 62273944 62273944 62273944 ACTGTCCTTCCAGTTGGGCTACAGTGAACTCCAGCTCTCGAATTCTTTGCTCCCTAGCTTTGATT ACTGTCCTTCCAGTTGGGCTACAGTGAACTCCGGCTCTCGAATTCTTTGCTCCCTAGCTTTGATT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:62273897..62274028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 3 bladder,urinary tract 110885 RMVar_ID_110885 Human_SNP_ID_805140061 m1A Human chr1 - 156009449 156009449 156009449 AGGTGCTTTCCAGACTCCAAAGGGTATCTTAAATGCAATCTCTTCTCTCTTAGCCCTTGGCCACT AGGTGCTTTCCAGACTCCAAAGGGTATCTTAAGTGCAATCTCTTCTCTCTTAGCCCTTGGCCACT T C SSR2 Ensembl:ENSG00000163479 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:156009401..156009475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_22873,Human_RBP_ID_328428,Human_RBP_ID_971682,Human_RBP_ID_3282960,Human_RBP_ID_4082593,Human_RBP_ID_5108795,Human_RBP_ID_5484543,Human_RBP_ID_8287043,Human_RBP_ID_17212828,Human_RBP_ID_17330656,Human_RBP_ID_17446615,Human_RBP_ID_17727151,Human_RBP_ID_18553061,Human_RBP_ID_24395535,Human_RBP_ID_26369471,Human_RBP_ID_27389206 Human_miRNA_ID_977960,Human_miRNA_ID_982693 RMVar_hsa_circ_77498,RMVar_hsa_circ_87891,RMVar_hsa_circ_120703,RMVar_hsa_circ_136754,RMVar_hsa_circ_136755,RMVar_hsa_circ_136753 110886 RMVar_ID_110886 Human_SNP_ID_805158076 m1A Human chr1 - 37692626 37692626 37692626 GATGGGGCAGGGAAGCAAGAAACTGGGTAGGGACGAGGAGGGCGGACGGGGACCACCCGAAGAAG GATGGGGCAGGGAAGCAAGAAACTGGGTAGGGGCGAGGAGGGCGGACGGGGACCACCCGAAGAAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:37692576..37692675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 110887 RMVar_ID_110887 Human_SNP_ID_805163403 m1A Human chr1 - 155834254 155834254 155834254 ACAAGGTACTTTAAAATGTAAATTTAAAATTTAGTAGCAAAGGAGGGATAAGGATAATACCTGAG ACAAGGTACTTTAAAATGTAAATTTAAAATTTGGTAGCAAAGGAGGGATAAGGATAATACCTGAG T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:155834252..155834394 26863196 MeRIP-seq:(Medium) rs1377417510 Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_348477,RMVar_hsa_circ_136712,RMVar_hsa_circ_71077,RMVar_hsa_circ_360729 110888 RMVar_ID_110888 Human_SNP_ID_805167243 m1A Human chr1 - 156594002 156594002 156594002 GCTGGTACTTCTTCTCCAGAGCAGGTGGCACAAAACGACCCCCCAGGTAATGGTAGCGACCGGTA GCTGGTACTTCTTCTCCAGAGCAGGTGGCACACAACGACCCCCCAGGTAATGGTAGCGACCGGTA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:156593951..156594125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - 110889 RMVar_ID_110889 Human_SNP_ID_805174022 m1A Human chr1 - 16623287 16623287 16623287 GATGGTTTTTAGATGATGGCTATACCATTTCCATTCCCTGTAGTCGTTTCCATTAATGCTGATAG GATGGTTTTTAGATGATGGCTATACCATTTCCGTTCCCTGTAGTCGTTTCCATTAATGCTGATAG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs9663022 Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_1073995,Human_RBP_ID_1728842,Human_RBP_ID_3286186,Human_RBP_ID_5092196,Human_RBP_ID_8979439,Human_RBP_ID_10648524,Human_RBP_ID_17072771,Human_RBP_ID_17339878,Human_RBP_ID_18219558 RMVar_hsa_circ_56321 110890 RMVar_ID_110890 Human_SNP_ID_805177582 m1A Human chr1 - 26863321 26863319 26863322 GGCTACTGAGAGCAGGTTTCGCTCTTCGCAGGAGAGCTCCTCGCCCTTCTCCACGGCGCCTTTCA GGCTACTGAGAGCAGGTTTCGCTCTTCGCAG___AGCTCCTCGCCCTTCTCCACGGCGCCTTTCA TCTC T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:26863151..26863536 26863196 MeRIP-seq:(Medium) rs1314504941 Functional Loss DEL TCGA 32..34 33 UCEC 1 - 110891 RMVar_ID_110891 Human_SNP_ID_805181810 m1A Human chr1 - 154597963 154597963 154597963 TGTCTCTCATTTTCTCTAGACTGCAGAGTCCCAGACCCCCACCCCTTCAGCCACATCCTTCTTTT TGTCTCTCATTTTCTCTAGACTGCAGAGTCCCGGACCCCCACCCCTTCAGCCACATCCTTCTTTT T C ADAR Ensembl:ENSG00000160710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:154597845..154598001 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_743718,Human_RBP_ID_802666,Human_RBP_ID_18552326,Human_RBP_ID_24591631 Human_Splice_Rec_134876,Human_Splice_Rec_134904,Human_Splice_Rec_134932,Human_Splice_Rec_134958,Human_Splice_Rec_134984,Human_Splice_Rec_135012,Human_Splice_Rec_135040,Human_Splice_Rec_135068,Human_Splice_Rec_135096,Human_Splice_Rec_135120,Human_Splice_Rec_135146,Human_Splice_Rec_135198,Human_Splice_Rec_135210 Human_miRNA_ID_2383581 RMVar_hsa_circ_127324,RMVar_hsa_circ_23411,RMVar_hsa_circ_105169,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_118402,RMVar_hsa_circ_136444,RMVar_hsa_circ_136446,RMVar_hsa_circ_136445,RMVar_hsa_circ_43148,RMVar_hsa_circ_301693,RMVar_hsa_circ_363758 110892 RMVar_ID_110892 Human_SNP_ID_805184299 m1A Human chr1 - 21176593 21176593 21176593 GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG GCGGCTGCTGCTGCCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGTCGGGCG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:21176440..21176768 26863196 MeRIP-seq:(Medium) rs1443808873 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 5 haematopoietic and lymphoid tissue Human_RBP_ID_95835,Human_RBP_ID_220805,Human_RBP_ID_4023942,Human_RBP_ID_5162058,Human_RBP_ID_8725021,Human_RBP_ID_21963894,Human_RBP_ID_24749305,Human_RBP_ID_26774119 RMVar_hsa_circ_93947,RMVar_hsa_circ_130010 110893 RMVar_ID_110893 Human_SNP_ID_805185697 m1A Human chr1 + 228298111 228298111 228298111 CTGTATGAGAATGGGAAGCAGGTGTCAGGACAAGGAGGTGCCTCCTGTGAGGCTGGAGAAAGAGA CTGTATGAGAATGGGAAGCAGGTGTCAGGACACGGAGGTGCCTCCTGTGAGGCTGGAGAAAGAGA A C OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:228297792..228298149 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 6 breast Human_miRNA_ID_2014786,Human_miRNA_ID_2254006,Human_miRNA_ID_2474139,Human_miRNA_ID_2959927 RMVar_hsa_circ_125472,RMVar_hsa_circ_140223,RMVar_hsa_circ_114219,RMVar_hsa_circ_76650,RMVar_hsa_circ_82487,RMVar_hsa_circ_140225,RMVar_hsa_circ_119575,RMVar_hsa_circ_140227,RMVar_hsa_circ_140228,RMVar_hsa_circ_102932,RMVar_hsa_circ_269226,RMVar_hsa_circ_268044,RMVar_hsa_circ_269610,RMVar_hsa_circ_140229,RMVar_hsa_circ_267468,RMVar_hsa_circ_10026,RMVar_hsa_circ_11932,RMVar_hsa_circ_140230,RMVar_hsa_circ_140231,RMVar_hsa_circ_123534,RMVar_hsa_circ_140232,RMVar_hsa_circ_115041,RMVar_hsa_circ_268744,RMVar_hsa_circ_26719,RMVar_hsa_circ_140233,RMVar_hsa_circ_26892,RMVar_hsa_circ_16610,RMVar_hsa_circ_15849,RMVar_hsa_circ_61789,RMVar_hsa_circ_140234 110894 RMVar_ID_110894 Human_SNP_ID_805214702 m1A Human chr1 - 228106821 228106821 228106821 TCAGCTCCAGTCGAGGAAGGAGTACGAGCAGGAGCTCAGTGATGACTTGCATGTGGAGCGCTACC TCAGCTCCAGTCGAGGAAGGAGTACGAGCAGGTGCTCAGTGATGACTTGCATGTGGAGCGCTACC T A MRPL55 Ensembl:ENSG00000162910 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:228106772..228106861 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 21 lung Human_RBP_ID_1739275,Human_RBP_ID_18565434,Human_RBP_ID_22871896 Human_Splice_Rec_194618,Human_Splice_Rec_194624,Human_Splice_Rec_194628,Human_Splice_Rec_194634,Human_Splice_Rec_194640,Human_Splice_Rec_194644,Human_Splice_Rec_194652,Human_Splice_Rec_194660,Human_Splice_Rec_194666,Human_Splice_Rec_194674,Human_Splice_Rec_194682,Human_Splice_Rec_194688,Human_Splice_Rec_194696,Human_Splice_Rec_194702,Human_Splice_Rec_194710,Human_Splice_Rec_194716,Human_Splice_Rec_194726,Human_Splice_Rec_194734,Human_Splice_Rec_194742,Human_Splice_Rec_194752,Human_Splice_Rec_194760,Human_Splice_Rec_194770 110895 RMVar_ID_110895 Human_SNP_ID_805242207 m1A Human chr1 + 225999293 225999293 225999293 TGCACCCGAAGCCAGGGCCGCGAATCCACACCAGCGCCGCGGCCTCCGCCATGTCACCGACTACC TGCACCCGAAGCCAGGGCCGCGAATCCACACCGGCGCCGCGGCCTCCGCCATGTCACCGACTACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:225999247..225999323 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 110896 RMVar_ID_110896 Human_SNP_ID_805246143 m1A Human chr1 - 84996982 84996982 84996982 AGAAAGGGTAAGAGAAGGGAACCCCGCTTTGCAGGGCTCCAACTTCGGCGGACGCGTTACGGCGA AGAAAGGGTAAGAGAAGGGAACCCCGCTTTGCCGGGCTCCAACTTCGGCGGACGCGTTACGGCGA T G MCOLN2 Ensembl:ENSG00000153898 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11161505 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LUSC 2 prostate GWAS_ID_7919,GWAS_ID_7920,GWAS_ID_7921,GWAS_ID_7922,GWAS_ID_7923,GWAS_ID_7924,GWAS_ID_7925,GWAS_ID_7926,GWAS_ID_7927 110897 RMVar_ID_110897 Human_SNP_ID_805251270 m1A Human chr1 - 207321827 207321827 207321827 CGGCCGGCAGGCACAACAGCACCAGCAGCAGCAGCCGGGGCAGCTCCCCGAGGAGGGGCAGCGCC CGGCCGGCAGGCACAACAGCACCAGCAGCAGCCGCCGGGGCAGCTCCCCGAGGAGGGGCAGCGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:207321776..207321875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 110898 RMVar_ID_110898 Human_SNP_ID_805263191 m1A Human chr1 - 154601491 154601491 154601491 TGAAACCGCTCCAGCTGCAATCCCTGAGACCAAAAGAAACGCAGAGTTCCTCACCTGTAATATAC TGAAACCGCTCCAGCTGCAATCCCTGAGACCAGAAGAAACGCAGAGTTCCTCACCTGTAATATAC T C ADAR Ensembl:ENSG00000160710 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2229857 Functional Loss SNV ICGC 33..33 33 COCA 6 - Human_RBP_ID_858053,Human_RBP_ID_8754143,Human_RBP_ID_17221650,Human_RBP_ID_19151593,Human_RBP_ID_21879230,Human_RBP_ID_26311876 Human_miRNA_ID_247398 Clinvar_Rec_531 GWAS_ID_12199,GWAS_ID_12200,GWAS_ID_12201,GWAS_ID_12202,GWAS_ID_12203,GWAS_ID_12204 RMVar_hsa_circ_127324,RMVar_hsa_circ_127688,RMVar_hsa_circ_136441,RMVar_hsa_circ_136446,RMVar_hsa_circ_301693,RMVar_hsa_circ_136454,RMVar_hsa_circ_324203,RMVar_hsa_circ_136455 110899 RMVar_ID_110899 Human_SNP_ID_805265678 m1A Human chr1 + 116570964 116570964 116570964 AGGACCCCCAGGGCCCGCCCCGCGTCGCTCCCAGCAACCATGGCTCGTCGGGCCGGCCTCTGCGC AGGACCCCCAGGGCCCGCCCCGCGTCGCTCCCGGCAACCATGGCTCGTCGGGCCGGCCTCTGCGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:116570758..116570965 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 110900 RMVar_ID_110900 Human_SNP_ID_805284074 m1A Human chr1 + 148522666 148522666 148522666 GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCATTGCGTTCCAGATGTGCTGACCTCTGCGATTT GAAGGCGCTTTTCTCATGGTCGCGGCTTATCCGTTGCGTTCCAGATGTGCTGACCTCTGCGATTT A G RNVU1-27 Ensembl:ENSG00000274210 snRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:148522601..148522750 26863196 MeRIP-seq:(Medium) rs1192439688 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_800737,Human_RBP_ID_1438979,Human_RBP_ID_1724708,Human_RBP_ID_2092181,Human_RBP_ID_5253989,Human_RBP_ID_8171179,Human_RBP_ID_8955497,Human_RBP_ID_9455487,Human_RBP_ID_10564040,Human_RBP_ID_17066651,Human_RBP_ID_17072900,Human_RBP_ID_17180773,Human_RBP_ID_17667605,Human_RBP_ID_17674908,Human_RBP_ID_17762845,Human_RBP_ID_18198321,Human_RBP_ID_18205224,Human_RBP_ID_18415047,Human_RBP_ID_18509888,Human_RBP_ID_18550575,Human_RBP_ID_19444789,Human_RBP_ID_21913510,Human_RBP_ID_22015540,Human_RBP_ID_22779667,Human_RBP_ID_22846371,Human_RBP_ID_23110089,Human_RBP_ID_23263638,Human_RBP_ID_23329922,Human_RBP_ID_24395306,Human_RBP_ID_26747257,Human_RBP_ID_26840581 110901 RMVar_ID_110901 Human_SNP_ID_805286780 m1A Human chr1 + 116392883 116392883 116392883 CAGCGGGCAGTTGCAGGAGATGCCTCTGAGTCAGCACTCTTAAAGTGCATAGAGCTGTGCTGTGG CAGCGGGCAGTTGCAGGAGATGCCTCTGAGTCCGCACTCTTAAAGTGCATAGAGCTGTGCTGTGG A C ATP1A1 Ensembl:ENSG00000163399 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:116390401..116392884 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 9 lung Human_RBP_ID_322792,Human_RBP_ID_744035,Human_RBP_ID_802573,Human_RBP_ID_857869,Human_RBP_ID_970312,Human_RBP_ID_1409247,Human_RBP_ID_1723216,Human_RBP_ID_3278008,Human_RBP_ID_5677021,Human_RBP_ID_8282161,Human_RBP_ID_8954534,Human_RBP_ID_9266124,Human_RBP_ID_17338348,Human_RBP_ID_17456526,Human_RBP_ID_17722555,Human_RBP_ID_18187227,Human_RBP_ID_18548546,Human_RBP_ID_19151226,Human_RBP_ID_22430809,Human_RBP_ID_22749377,Human_RBP_ID_22779267,Human_RBP_ID_22872400,Human_RBP_ID_23325829,Human_RBP_ID_26838566,Human_RBP_ID_27165702 Human_Splice_Rec_113830,Human_Splice_Rec_113878,Human_Splice_Rec_113932 Human_miRNA_ID_2453175,Human_miRNA_ID_2773103,Human_miRNA_ID_2948237 RMVar_hsa_circ_12349,RMVar_hsa_circ_358341,RMVar_hsa_circ_352627,RMVar_hsa_circ_108021,RMVar_hsa_circ_26347,RMVar_hsa_circ_6438,RMVar_hsa_circ_85489,RMVar_hsa_circ_78811,RMVar_hsa_circ_135609,RMVar_hsa_circ_135612,RMVar_hsa_circ_81548,RMVar_hsa_circ_85431,RMVar_hsa_circ_135615,RMVar_hsa_circ_135616,RMVar_hsa_circ_135614,RMVar_hsa_circ_64344,RMVar_hsa_circ_26648,RMVar_hsa_circ_79949,RMVar_hsa_circ_83686,RMVar_hsa_circ_104205,RMVar_hsa_circ_135617,RMVar_hsa_circ_135618,RMVar_hsa_circ_135620,RMVar_hsa_circ_135619,RMVar_hsa_circ_371218,RMVar_hsa_circ_112954,RMVar_hsa_circ_5028,RMVar_hsa_circ_135621 110902 RMVar_ID_110902 Human_SNP_ID_805317896 m1A Human chr1 - 156811891 156811891 156811891 TTGAGAGTCACCAGCACTTAGATGGACTCTAAAACCTTTAGGAGGGGAGAAATCTCACTCGGAAG TTGAGAGTCACCAGCACTTAGATGGACTCTAACACCTTTAGGAGGGGAGAAATCTCACTCGGAAG T G SH2D2A Ensembl:ENSG00000027869 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:156811889..156811997 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 110903 RMVar_ID_110903 Human_SNP_ID_805322335 m1A Human chr1 - 149967425 149967425 149967425 TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCAATGAGCACCCCCTGGAAATGCCCATCTGTGCCT TGTCTCCTCCAATGGTGGGGGTGGGGGGAGCAGTGAGCACCCCCTGGAAATGCCCATCTGTGCCT T C OTUD7B Ensembl:ENSG00000264522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:149967376..149967458 26863196 MeRIP-seq:(Medium) rs1553776847 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma,large_intestine adenocarcinoma 2 head and neck,large intestine Human_RBP_ID_223296 Human_Splice_Rec_125498,Human_Splice_Rec_125520 RMVar_hsa_circ_135866,RMVar_hsa_circ_335443,RMVar_hsa_circ_359311,RMVar_hsa_circ_289132,RMVar_hsa_circ_337125,RMVar_hsa_circ_102415,RMVar_hsa_circ_44952,RMVar_hsa_circ_308460,RMVar_hsa_circ_346535,RMVar_hsa_circ_276934 110904 RMVar_ID_110904 Human_SNP_ID_805334424 m1A Human chr1 + 152036963 152036961 152036963 GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCTGAGAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG GGCGCGGGAGGCTGTGGCTGGGAGCGGCGCT__GAGCTCTGTGCGCGCGGCGTGCGGGTCTGGAG TGA T AL450992.2 Ensembl:ENSG00000229021 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr1:152036818..152037025;chr1:152036870..152037025 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 CHOL 1 - 110905 RMVar_ID_110905 Human_SNP_ID_805334784 m1A Human chr1 - 89104519 89104519 89104519 ATTTTATGTTGTTTACGAAAAGGAGAATCTGGACAGTCATGGCCAAGGTTAACAAAAGAAAGGGC ATTTTATGTTGTTTACGAAAAGGAGAATCTGGCCAGTCATGGCCAAGGTTAACAAAAGAAAGGGC T G PTGES3P1 Ensembl:ENSG00000234518 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879140598 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_miRNA_ID_1840880,Human_miRNA_ID_1855136 110906 RMVar_ID_110906 Human_SNP_ID_805341740 m1A Human chr1 - 23825310 23825306 23825310 GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTGACTGTCAGGGTTGGGGGCTTGGCCCGTGGTGAC GCCGCCGAGGCGGCGGCCCTGCAGGCACTCTG____TCAGGGTTGGGGGCTTGGCCCGTGGTGAC ACAGT A HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:23825308..23825401 26863196 MeRIP-seq:(Medium) rs1445836005 Functional Loss DEL ICGC 33..36 33 STAD 1 - Human_RBP_ID_100637 RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 110907 RMVar_ID_110907 Human_SNP_ID_805345235 m1A Human chr1 + 205228009 205228009 205228009 CGGCTTTGCGGCAGGCTGCGCGTCAGGCGGGGAGCGGGGCGCGCGGGCCGGGGAGGGGGCCGGGC CGGCTTTGCGGCAGGCTGCGCGTCAGGCGGGGGGCGGGGCGCGCGGGCCGGGGAGGGGGCCGGGC A G TMCC2 Ensembl:ENSG00000133069 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:205227968..205228061 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110908 RMVar_ID_110908 Human_SNP_ID_805352025 m1A Human chr1 + 26189373 26189373 26189373 GAAGTTCCGCCAGTGGAAGGAGCAGAACCGGGAGCTGTACTCAGAGGGCCTGGGGGCCTGGGGAG GAAGTTCCGCCAGTGGAAGGAGCAGAACCGGGGGCTGTACTCAGAGGGCCTGGGGGCCTGGGGAG A G CNKSR1 Ensembl:ENSG00000142675 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:26189322..26189431 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 colon adenocarcinoma,UCEC,large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_33348,Human_Splice_Rec_33392,Human_Splice_Rec_33456,Human_Splice_Rec_33494 110909 RMVar_ID_110909 Human_SNP_ID_805359373 m1A Human chr1 - 220528400 220528399 220528400 GGCTCGTCCTGGCGAGCGCCTGGGCGTCAGGAACCGCGGCCCTGACAGCGTCACCCGCGCCGCGC GGCTCGTCCTGGCGAGCGCCTGGGCGTCAGGA_CCGCGGCCCTGACAGCGTCACCCGCGCCGCGC GT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:220528232..220528431 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 RECA 1 - 110910 RMVar_ID_110910 Human_SNP_ID_805373979 m1A Human chr1 - 241504132 241504132 241504132 ACACTACTGCCTGCAGTCTGATGAAGATAGCAAATGATATTCGATTTTTGGGTTCTGGTCCTCGG ACACTACTGCCTGCAGTCTGATGAAGATAGCAGATGATATTCGATTTTTGGGTTCTGGTCCTCGG T C FH Ensembl:ENSG00000091483 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:241504013..241504160 26863196 MeRIP-seq:(Medium) rs775639021 Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 1 breast Human_Splice_Rec_205437 Human_miRNA_ID_1782120,Human_miRNA_ID_2915360,Human_miRNA_ID_2989355 RMVar_hsa_circ_62661,RMVar_hsa_circ_62778,RMVar_hsa_circ_268703,RMVar_hsa_circ_312676,RMVar_hsa_circ_92290,RMVar_hsa_circ_105614,RMVar_hsa_circ_141076,RMVar_hsa_circ_23884,RMVar_hsa_circ_365166,RMVar_hsa_circ_101299,RMVar_hsa_circ_141078,RMVar_hsa_circ_141080,RMVar_hsa_circ_88521,RMVar_hsa_circ_141079,RMVar_hsa_circ_141077 110911 RMVar_ID_110911 Human_SNP_ID_805392132 m1A Human chr1 + 1232799 1232791 1232799 GGACGCGCTGCTGGCCGAGCTGCGCGCCCGCGAGCCCGCGCGCCGCCGCCGCCTCTACTGGGGCT GGACGCGCTGCTGGCCGAGCTGCGC________GCCCGCGCGCCGCCGCCGCCTCTACTGGGGCT CGCCCGCGA C B3GALT6 Ensembl:ENSG00000176022 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1232767..1232885 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 26..33 33 ESCA 1 - 110912 RMVar_ID_110912 Human_SNP_ID_805400058 m1A Human chr1 - 167787891 167787891 167787891 TCTTAATTCTTTCGGATATCCGCATACACCACAGACTCTGACTTGTTAATCTTGTCACTGTGATG TCTTAATTCTTTCGGATATCCGCATACACCACGGACTCTGACTTGTTAATCTTGTCACTGTGATG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:167787840..167787941 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 110913 RMVar_ID_110913 Human_SNP_ID_805401948 m1A Human chr1 - 234610001 234610001 234610001 GCGCCCGAGCTCCACGCCGCCCGGCCGCCGCCACCCCGGCGCGGCATGCCCCGCCGCTCGGGCTG GCGCCCGAGCTCCACGCCGCCCGGCCGCCGCCCCCCCGGCGCGGCATGCCCCGCCGCTCGGGCTG T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,untreat control chr1:234609401..234610175;chr1:234609736..234610126 26863410 MeRIP-seq:(Medium) rs911639353 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110914 RMVar_ID_110914 Human_SNP_ID_805418828 m1A Human chr1 - 170074526 170074526 170074526 GGTGTGAGGGTACTTTGGCCACCGTCCCCGGAAATAACCGCGCCTGCCTCTCAAGATACCCCATC GGTGTGAGGGTACTTTGGCCACCGTCCCCGGAGATAACCGCGCCTGCCTCTCAAGATACCCCATC T C KIFAP3 Ensembl:ENSG00000075945 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:170074476..170074669 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4084765,Human_RBP_ID_26801268 Human_Splice_Rec_156497,Human_Splice_Rec_156531,Human_Splice_Rec_156567 110915 RMVar_ID_110915 Human_SNP_ID_805428234 m1A Human chr1 + 6142598 6142598 6142598 AGTCGATGTACCATGGCTGCTTGTCGAACTTGACCGTGGGCTGCAGGGGAGGCAGCGGTTCAGAC AGTCGATGTACCATGGCTGCTTGTCGAACTTGGCCGTGGGCTGCAGGGGAGGCAGCGGTTCAGAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:6142549..6143867 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 110916 RMVar_ID_110916 Human_SNP_ID_805442349 m1A Human chr1 + 6857178 6857178 6857178 TGGGTGCAATTTGCAGGAATCCAGTGAAAGTTAACGGTGGAGGTGGCGCCAAGGCCCAGCAGTGG TGGGTGCAATTTGCAGGAATCCAGTGAAAGTTCACGGTGGAGGTGGCGCCAAGGCCCAGCAGTGG A C CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:6857176..6857247 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_64611,RMVar_hsa_circ_128681,RMVar_hsa_circ_86544,RMVar_hsa_circ_128682,RMVar_hsa_circ_110317,RMVar_hsa_circ_82278,RMVar_hsa_circ_61652,RMVar_hsa_circ_128685,RMVar_hsa_circ_128686 110917 RMVar_ID_110917 Human_SNP_ID_805451931 m1A Human chr1 + 822829 822829 822829 CTGTCTACACTACCTGCTTGCCCAGCAGGTCCACCCTATCTACACTACCTGCCTGCCCAGCAGAT CTGTCTACACTACCTGCTTGCCCAGCAGGTCCGCCCTATCTACACTACCTGCCTGCCCAGCAGAT A G lnc-SAMD11-4,FAM87B RNACentral:URS00008BAC85,RNACentral:URS00008B5E4E lincRNA,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr1:822795..822924 26863196 MeRIP-seq:(Medium) rs1404788698 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110918 RMVar_ID_110918 Human_SNP_ID_805475408 m1A Human chr1 + 156935843 156935843 156935843 GAAACCTGACTCCGACTTGAGCAGACCAAGCAACATGCGGGTCTCCCCCCGGGCCTTGGCTGGAT GAAACCTGACTCCGACTTGAGCAGACCAAGCAGCATGCGGGTCTCCCCCCGGGCCTTGGCTGGAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:156935793..156935902 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 face Merkel_cell_carcinoma,COCA,skin Merkel_cell_carcinoma 3 skin,head and neck 110919 RMVar_ID_110919 Human_SNP_ID_805482594 m1A Human chr1 + 21830041 21830041 21830041 CCCCGAGCGGCCCAGGTGGCAGCGGCAGGTGTAGCCTCGACCGTCAGGCCGGTTCACACAGGTGG CCCCGAGCGGCCCAGGTGGCAGCGGCAGGTGTTGCCTCGACCGTCAGGCCGGTTCACACAGGTGG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:21829976..21830100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110920 RMVar_ID_110920 Human_SNP_ID_805484464 m1A Human chr1 + 40097198 40097198 40097198 GCAGCGCCCGAGAAGCGCAGGTCCATGGCAGGAGAGCCACAGCCAAGAGCCACAGGCAGCCGGGC GCAGCGCCCGAGAAGCGCAGGTCCATGGCAGGGGAGCCACAGCCAAGAGCCACAGGCAGCCGGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:40097067..40097250;chr1:40097075..40097250;chr1:40097058..40097250;chr1:40097074..40097250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 110921 RMVar_ID_110921 Human_SNP_ID_805488175 m1A Human chr1 + 150472250 150472250 150472250 TCACAGTGCATCCAATAGGAGGATGTCAGGGGAGCCGATCCAGACCGTAGAGTCCATCCGAGTTC TCACAGTGCATCCAATAGGAGGATGTCAGGGGTGCCGATCCAGACCGTAGAGTCCATCCGAGTTC A T RPRD2 Ensembl:ENSG00000163125 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:150472201..150472394 26863196 MeRIP-seq:(Medium) rs1156611385 Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_2093074,Human_RBP_ID_5686950,Human_RBP_ID_22023760 110922 RMVar_ID_110922 Human_SNP_ID_805488370 m1A Human chr1 - 155250448 155250448 155250448 TTCCCCGAGCTGAGGCGGCGGGTCCCCCGGGGAGGGGGCCGCCCAGCCGCAGCCCCGCCCACCCG TTCCCCGAGCTGAGGCGGCGGGTCCCCCGGGGGGGGGGCCGCCCAGCCGCAGCCCCGCCCACCCG T C FAM189B Ensembl:ENSG00000160767 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:155250276..155250700 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_803577 RMVar_hsa_circ_87969,RMVar_hsa_circ_124894,RMVar_hsa_circ_136533,RMVar_hsa_circ_136534 110923 RMVar_ID_110923 Human_SNP_ID_805492035 m1A Human chr1 - 1341782 1341782 1341782 CCCCCACAGCCGCCCGGACCAATGGGCACCCAAGGGGAGACCGACGGCGGGATGTGGGGCTGCCC CCCCCACAGCCGCCCGGACCAATGGGCACCCAGGGGGAGACCGACGGCGGGATGTGGGGCTGCCC T C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:1341672..1341834 26863196 MeRIP-seq:(Medium) rs376205129 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_myelomonocytic_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_3988689,Human_RBP_ID_5432789,Human_RBP_ID_5484170 Human_Splice_Rec_3536,Human_Splice_Rec_3564,Human_Splice_Rec_3592 RMVar_hsa_circ_26266,RMVar_hsa_circ_120031,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_121380,RMVar_hsa_circ_32455,RMVar_hsa_circ_128317,RMVar_hsa_circ_23178,RMVar_hsa_circ_372589,RMVar_hsa_circ_128321,RMVar_hsa_circ_128322 110924 RMVar_ID_110924 Human_SNP_ID_805510849 m1A Human chr1 - 215567351 215567351 215567351 AGCCTGCCTGGGAGGAGGGGTCACCGTTCGGGACAAAATACCGCAGCGCTCACGCTTCGCCCGCC AGCCTGCCTGGGAGGAGGGGTCACCGTTCGGGGCAAAATACCGCAGCGCTCACGCTTCGCCCGCC T C lnc-USH2A-1 RNACentral:URS00008BE2D0 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:215567301..215567457 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 110925 RMVar_ID_110925 Human_SNP_ID_805522237 m1A Human chr1 - 109411065 109411065 109411065 TCTGGGACCTTTGTACAGTGTGATGCTCGAGCAATTGGCTCTGCTTCAGAGGGTGCCCAGAGCTC TCTGGGACCTTTGTACAGTGTGATGCTCGAGCTATTGGCTCTGCTTCAGAGGGTGCCCAGAGCTC T A PSMA5 Ensembl:ENSG00000143106 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:109410002..109411971 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 2 head and neck Human_RBP_ID_320289,Human_RBP_ID_1407671,Human_RBP_ID_3936378,Human_RBP_ID_5666584,Human_RBP_ID_8280220,Human_RBP_ID_8953563,Human_RBP_ID_10507835,Human_RBP_ID_18965768,Human_RBP_ID_22427351,Human_RBP_ID_22870914,Human_RBP_ID_23321149,Human_RBP_ID_26767540 Human_Splice_Rec_105960,Human_Splice_Rec_105961,Human_Splice_Rec_105976,Human_Splice_Rec_105977,Human_Splice_Rec_105992,Human_Splice_Rec_105993 RMVar_hsa_circ_104745,RMVar_hsa_circ_135214,RMVar_hsa_circ_282746,RMVar_hsa_circ_348759,RMVar_hsa_circ_370671,RMVar_hsa_circ_301761,RMVar_hsa_circ_121549,RMVar_hsa_circ_135212,RMVar_hsa_circ_135213,RMVar_hsa_circ_135211,RMVar_hsa_circ_135215 110926 RMVar_ID_110926 Human_SNP_ID_805522911 m1A Human chr1 + 6633037 6633037 6633037 GTCCAGCCGCCTCCGTGCTTGCAAAGGGCACCAGGGACTCCAGGCCAGACTTGGGCCAGAGCAGC GTCCAGCCGCCTCCGTGCTTGCAAAGGGCACCGGGGACTCCAGGCCAGACTTGGGCCAGAGCAGC A G THAP3 Ensembl:ENSG00000041988 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3174820 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue GWAS_ID_7969,GWAS_ID_7970,GWAS_ID_7971,GWAS_ID_7972,GWAS_ID_7973,GWAS_ID_7974,GWAS_ID_7975,GWAS_ID_7976,GWAS_ID_7977,GWAS_ID_7978,GWAS_ID_7979,GWAS_ID_7980,GWAS_ID_7981,GWAS_ID_7982,GWAS_ID_7983,GWAS_ID_7984,GWAS_ID_7985,GWAS_ID_7986,GWAS_ID_7987,GWAS_ID_7988,GWAS_ID_7989,GWAS_ID_7990,GWAS_ID_7991,GWAS_ID_7992,GWAS_ID_7993,GWAS_ID_7994,GWAS_ID_7995,GWAS_ID_7996,GWAS_ID_7997,GWAS_ID_7998,GWAS_ID_7999,GWAS_ID_8000,GWAS_ID_8001,GWAS_ID_8002,GWAS_ID_8003,GWAS_ID_8004,GWAS_ID_8005,GWAS_ID_8006,GWAS_ID_8007,GWAS_ID_8008,GWAS_ID_8009,GWAS_ID_8010,GWAS_ID_8011,GWAS_ID_8012,GWAS_ID_8013,GWAS_ID_8014,GWAS_ID_8015,GWAS_ID_8016,GWAS_ID_8017,GWAS_ID_8018,GWAS_ID_8019,GWAS_ID_8020 110927 RMVar_ID_110927 Human_SNP_ID_805527401 m1A Human chr1 - 153728697 153728697 153728697 CCTGGGGCTCCTGCTCCCGCTCCTCCTCCTCCACCTCCCGCTGCTCCCGAAGCAGCTGCTGCTGC CCTGGGGCTCCTGCTCCCGCTCCTCCTCCTCCCCCTCCCGCTGCTCCCGAAGCAGCTGCTGCTGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:153728648..153728748 26863196 MeRIP-seq:(Medium) rs1557982839 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung 110928 RMVar_ID_110928 Human_SNP_ID_805530570 m1A Human chr1 - 15944406 15944406 15944406 GCACAGCGGCGAGAAGCCCTACCAGTGCGACTACTGCGGCCGCTCCTTCTCCGACCCCACTTCCA GCACAGCGGCGAGAAGCCCTACCAGTGCGACTGCTGCGGCCGCTCCTTCTCCGACCCCACTTCCA T C ZBTB17 Ensembl:ENSG00000116809 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:15944355..15944437 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_27390488 RMVar_hsa_circ_13802,RMVar_hsa_circ_57754,RMVar_hsa_circ_129502,RMVar_hsa_circ_21769,RMVar_hsa_circ_272315 110929 RMVar_ID_110929 Human_SNP_ID_805532869 m1A Human chr1 - 23559343 23559343 23559343 TCGGAACGCAGTCTGGCCATCGCCCGGGGCCGAGGGAAGGGCCCGGCAGCTGAGGAGCCGCTGAG TCGGAACGCAGTCTGGCCATCGCCCGGGGCCGCGGGAAGGGCCCGGCAGCTGAGGAGCCGCTGAG T G ID3 Ensembl:ENSG00000117318 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr1:23558944..23559500;chr1:23559126..23559475 32194978 MeRIP-seq:(Medium) rs761142520 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_1154,Human_RBP_ID_347768,Human_RBP_ID_1254178,Human_RBP_ID_4073670,Human_RBP_ID_18967605,Human_RBP_ID_22428210,Human_RBP_ID_22750862,Human_RBP_ID_22871728,Human_RBP_ID_27178965 Human_miRNA_ID_2239960 RMVar_hsa_circ_124280,RMVar_hsa_circ_130477 110930 RMVar_ID_110930 Human_SNP_ID_805543523 m1A Human chr1 - 236555835 236555835 236555835 CATCAGTCTCAGCTAACCGCCTTTTTCCTGGAAGCCCTGGACTTCCGAGCCCAGCACTCTGAGGT CATCAGTCTCAGCTAACCGCCTTTTTCCTGGAGGCCCTGGACTTCCGAGCCCAGCACTCTGAGGT T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1885532 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_221621,Human_RBP_ID_3937516,Human_RBP_ID_8754489,Human_RBP_ID_9271869,Human_RBP_ID_9357684,Human_RBP_ID_18966545,Human_RBP_ID_26767646 Human_Splice_Rec_203329,Human_Splice_Rec_203415 RMVar_hsa_circ_4051,RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_61188,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840,RMVar_hsa_circ_336753,RMVar_hsa_circ_374278,RMVar_hsa_circ_120373,RMVar_hsa_circ_140843,RMVar_hsa_circ_140844,RMVar_hsa_circ_140845 110931 RMVar_ID_110931 Human_SNP_ID_805546670 m1A Human chr1 - 11806272 11806272 11806272 CCACCTGCAGCAGCAGCACAGAGACCCCCTGCACCCCGCCATCTTCCTCCTTTACTGCCACTCTG CCACCTGCAGCAGCAGCACAGAGACCCCCTGCCCCCCGCCATCTTCCTCCTTTACTGCCACTCTG T G MTHFR Ensembl:ENSG00000177000 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:11806223..11807200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110932 RMVar_ID_110932 Human_SNP_ID_805548233 m1A Human chr1 - 16914139 16914129 16914139 GCCCCCGCGCACGCGCGCGCCCCCGGCCACCTACCTTCGCGCGCCTTCGCCGCAGCCGCTGCTGC GCCCCCGCGCACGCGCGCGCCCCCGGCCACCT__________GCCTTCGCCGCAGCCGCTGCTGC CGCGCGAAGGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:16914092..16914324;chr1:16914090..16914260 26863196 MeRIP-seq:(Medium) rs149234723 Functional Loss DEL ICGC 33..42 33 MELA 1 - 110933 RMVar_ID_110933 Human_SNP_ID_805576309 m1A Human chr1 - 632981 632981 632981 ATGTAAAGGATGCGTAGGGATGGGAGGGCGATAAGGACTAGGATGATGGCGGGCAGGATAGTTCA ATGTAAAGGATGCGTAGGGATGGGAGGGCGATGAGGACTAGGATGATGGCGGGCAGGATAGTTCA T C AL669831.3 Ensembl:ENSG00000230021 Pseudogene intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:632902..633049 26863196 MeRIP-seq:(Medium) rs4098613 Functional Loss SNV ICGC 33..33 33 LMS 3 - Human_RBP_ID_4077356,Human_RBP_ID_5843547,Human_RBP_ID_17340733,Human_RBP_ID_18509609,Human_RBP_ID_18523586,Human_RBP_ID_23255425 110934 RMVar_ID_110934 Human_SNP_ID_805576590 m1A Human chr1 - 156572515 156572515 156572515 CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCAGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG CCTGGAAGAAGGAGGAACATGGAGAGGAGAGCTGCGGGCCCAGGCTGGGCAGCCTGTGAGTGCGG T A IQGAP3 Ensembl:ENSG00000183856 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr1:156566376..156572586;chr1:156566395..156572575 26863196 MeRIP-seq:(Medium) rs140461633 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_222985,Human_RBP_ID_18415655,Human_RBP_ID_18969179,Human_RBP_ID_22637656,Human_RBP_ID_24541229,Human_RBP_ID_26312017,Human_RBP_ID_27798663 Human_Splice_Rec_142945,Human_Splice_Rec_143017 RMVar_hsa_circ_128164,RMVar_hsa_circ_136869 110935 RMVar_ID_110935 Human_SNP_ID_805576636 m1A Human chr1 - 117077992 117077992 117077992 TCTGCCACAACCGTCTCACCAGGACATGACTCAAGTGAGCGATGCAGTTGACCGATGGCTTCACT TCTGCCACAACCGTCTCACCAGGACATGACTCGAGTGAGCGATGCAGTTGACCGATGGCTTCACT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:117077946..117081848 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 110936 RMVar_ID_110936 Human_SNP_ID_805576671 m1A Human chr1 + 923980 923980 923980 CCGGGCGGGCGCGCGCCAGTGGACGCGGGTGCACGACTGACGCGGCCCGGGCGGCGGGGCGGGGG CCGGGCGGGCGCGCGCCAGTGGACGCGGGTGCTCGACTGACGCGGCCCGGGCGGCGGGGCGGGGG A T SAMD11 Ensembl:ENSG00000187634 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:923926..924450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 110937 RMVar_ID_110937 Human_SNP_ID_805630395 m1A Human chr1 + 42766633 42766633 42766633 AGGCAGCGGCGCAGGCAGGCAGCGCGACGCAGAAGGCCCCCGAAGAAGCTCAGGTCGCGCAGGGC AGGCAGCGGCGCAGGCAGGCAGCGCGACGCAGTAGGCCCCCGAAGAAGCTCAGGTCGCGCAGGGC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:42766501..42766934 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary 110938 RMVar_ID_110938 Human_SNP_ID_805657580 m1A Human chr1 - 31059253 31059250 31059253 GGGAGGAGGAAGTGGAGGAGGCGGCTATAATAATAGCAAACATCGATGGCCTACTGGGGATAACA GGGAGGAGGAAGTGGAGGAGGCGGCTATAATA___GCAAACATCGATGGCCTACTGGGGATAACA CTAT C PUM1 Ensembl:ENSG00000134644 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:31007081..31059327;chr1:31007081..31059300 26863196 MeRIP-seq:(Medium) rs1378499024 Functional Loss DEL TCGA 33..35 33 STAD 1 - Human_RBP_ID_1745213,Human_RBP_ID_2142794,Human_RBP_ID_3309718,Human_RBP_ID_3933136,Human_RBP_ID_4093894,Human_RBP_ID_5518753,Human_RBP_ID_9562932,Human_RBP_ID_10930842,Human_RBP_ID_17748457,Human_RBP_ID_18430141,Human_RBP_ID_18967797,Human_RBP_ID_22874839,Human_RBP_ID_24763952,Human_RBP_ID_26310720,Human_RBP_ID_26861953,Human_RBP_ID_27797707 Human_Splice_Rec_39917,Human_Splice_Rec_39951,Human_Splice_Rec_39993,Human_Splice_Rec_40035,Human_Splice_Rec_40075,Human_Splice_Rec_40149,Human_Splice_Rec_40191,Human_Splice_Rec_40233,Human_Splice_Rec_40359,Human_Splice_Rec_40371 Human_miRNA_ID_1976370,Human_miRNA_ID_1976371 RMVar_hsa_circ_83915,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_131001,RMVar_hsa_circ_53855,RMVar_hsa_circ_82449,RMVar_hsa_circ_118532,RMVar_hsa_circ_131026,RMVar_hsa_circ_131027,RMVar_hsa_circ_116734,RMVar_hsa_circ_355888,RMVar_hsa_circ_131034,RMVar_hsa_circ_131035,RMVar_hsa_circ_64820,RMVar_hsa_circ_329239,RMVar_hsa_circ_131040,RMVar_hsa_circ_41241,RMVar_hsa_circ_298085,RMVar_hsa_circ_131042,RMVar_hsa_circ_131041,RMVar_hsa_circ_271456,RMVar_hsa_circ_131043,RMVar_hsa_circ_271730 110939 RMVar_ID_110939 Human_SNP_ID_805667647 m1A Human chr1 - 145927053 145927053 145927053 GGTTCCAGAGAGCATTCACAAACTGAAAGAAAAAGCGAAGAAACGGAAGGGTCGCGGCTTTGGCT GGTTCCAGAGAGCATTCACAAACTGAAAGAAACAGCGAAGAAACGGAAGGGTCGCGGCTTTGGCT T G RBM8A Ensembl:ENSG00000265241 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:145926986..145927125 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_855112,Human_RBP_ID_5136337,Human_RBP_ID_5331874,Human_RBP_ID_9356738,Human_RBP_ID_18415041,Human_RBP_ID_18968772,Human_RBP_ID_22429625,Human_RBP_ID_22871370,Human_RBP_ID_23329143,Human_RBP_ID_24541825,Human_RBP_ID_26309796 Human_Splice_Rec_118872,Human_Splice_Rec_118873,Human_Splice_Rec_118882,Human_Splice_Rec_118883,Human_Splice_Rec_118894,Human_Splice_Rec_118895,Human_Splice_Rec_118904,Human_Splice_Rec_118908,Human_Splice_Rec_118914 RMVar_hsa_circ_49099 110940 RMVar_ID_110940 Human_SNP_ID_805670896 m1A Human chr1 + 167776129 167776129 167776129 GCAGGCTCCTCGGAAGTCCCCCTCCGACACTGAGGGTCTTGTAAAGAGTCTGCCTTCTGGATCTC GCAGGCTCCTCGGAAGTCCCCCTCCGACACTGGGGGTCTTGTAAAGAGTCTGCCTTCTGGATCTC A G MPZL1 Ensembl:ENSG00000197965 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:167776101..167776175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_22750387,Human_RBP_ID_24746100 Human_Splice_Rec_154466,Human_Splice_Rec_154467,Human_Splice_Rec_154474,Human_Splice_Rec_154475,Human_Splice_Rec_154500,Human_Splice_Rec_154501,Human_Splice_Rec_154510,Human_Splice_Rec_154511 Human_miRNA_ID_2930779,Human_miRNA_ID_2930780 RMVar_hsa_circ_269973,RMVar_hsa_circ_377373,RMVar_hsa_circ_137351,RMVar_hsa_circ_137352,RMVar_hsa_circ_137350,RMVar_hsa_circ_376544,RMVar_hsa_circ_270834,RMVar_hsa_circ_137357,RMVar_hsa_circ_137358,RMVar_hsa_circ_377237 110941 RMVar_ID_110941 Human_SNP_ID_805672430 m1A Human chr1 - 156137030 156137030 156137030 GCCTCCCCAGAGTCCCAAGCGCCCTGCCACTCACCGTCACCACCTGCCCAGCCTTCAGGGTGAAC GCCTCCCCAGAGTCCCAAGCGCCCTGCCACTCCCCGTCACCACCTGCCCAGCCTTCAGGGTGAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156137001..156137122 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 10 stomach 110942 RMVar_ID_110942 Human_SNP_ID_805689625 m1A Human chr1 + 63634928 63634928 63634928 CTGCGTTCCTCTGGAGGACTTTGGAGGCCACCACCCTGACCCCAACCTCACCTATGCAGCTGACC CTGCGTTCCTCTGGAGGACTTTGGAGGCCACCGCCCTGACCCCAACCTCACCTATGCAGCTGACC A G PGM1 Ensembl:ENSG00000079739 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:63634879..63635047 26863196 MeRIP-seq:(Medium) rs1164462551 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 3 head and neck Human_RBP_ID_18968505 Human_Splice_Rec_81166,Human_Splice_Rec_81167,Human_Splice_Rec_81184,Human_Splice_Rec_81185,Human_Splice_Rec_81202,Human_Splice_Rec_81203,Human_Splice_Rec_81222,Human_Splice_Rec_81223 Human_miRNA_ID_2006168,Human_miRNA_ID_2006169 RMVar_hsa_circ_85104,RMVar_hsa_circ_88997,RMVar_hsa_circ_133611,RMVar_hsa_circ_133609,RMVar_hsa_circ_133610,RMVar_hsa_circ_299954,RMVar_hsa_circ_310052,RMVar_hsa_circ_369039,RMVar_hsa_circ_133612,RMVar_hsa_circ_65619,RMVar_hsa_circ_22049,RMVar_hsa_circ_72555 110943 RMVar_ID_110943 Human_SNP_ID_805700863 m1A Human chr1 - 244864411 244864411 244864411 TGCAGCACGAACCCATCTCCAGCCGCAGCCGCAGCCGCCGCCCGGGCCGAGGAGCAGCCGCAGCA TGCAGCACGAACCCATCTCCAGCCGCAGCCGCCGCCGCCGCCCGGGCCGAGGAGCAGCCGCAGCA T G HNRNPU Ensembl:ENSG00000153187 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:244864176..244864525 26863410 MeRIP-seq:(Medium) rs1033668812 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_25253,Human_RBP_ID_224241,Human_RBP_ID_1743560,Human_RBP_ID_4074898,Human_RBP_ID_5797486,Human_RBP_ID_9357746,Human_RBP_ID_17746350,Human_RBP_ID_18569640,Human_RBP_ID_22532007,Human_RBP_ID_24541403,Human_RBP_ID_26309920,Human_RBP_ID_26859465,Human_RBP_ID_27179600,Human_RBP_ID_27801782 110944 RMVar_ID_110944 Human_SNP_ID_805702818 m1A Human chr1 + 65067681 65067681 65067681 CTATTTGCATGAGGATTATCTAATGACGCAGCAAGGCTCGCCACAACGTGACCGTCGCCATTTTT CTATTTGCATGAGGATTATCTAATGACGCAGCGAGGCTCGCCACAACGTGACCGTCGCCATTTTT A G lnc-AK4-1 RNACentral:URS0000D5D7C7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:65067228..65067721 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 110945 RMVar_ID_110945 Human_SNP_ID_805713936 m1A Human chr1 - 220058802 220058802 220058802 TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs3201546 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 110946 RMVar_ID_110946 Human_SNP_ID_805715872 m1A Human chr1 + 228140356 228140355 228140356 GGGCTGGCTGCGGCCGCCCTGGGCCGGGCCCCACCGGACGGTGAGTACGACAAGCGCGATCGCGA GGGCTGGCTGCGGCCGCCCTGGGCCGGGCCCC_CCGGACGGTGAGTACGACAAGCGCGATCGCGA CA C GUK1 Ensembl:ENSG00000143774 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr1:228140251..228141187 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LIHC 1 - Human_RBP_ID_4073308,Human_RBP_ID_5109818,Human_RBP_ID_5136505,Human_RBP_ID_18415724,Human_RBP_ID_19040362,Human_RBP_ID_22024321,Human_RBP_ID_22871070 Human_Splice_Rec_194835,Human_Splice_Rec_194845,Human_Splice_Rec_194859,Human_Splice_Rec_194869,Human_Splice_Rec_194881,Human_Splice_Rec_194883,Human_Splice_Rec_194889,Human_Splice_Rec_194903,Human_Splice_Rec_194919,Human_Splice_Rec_194935,Human_Splice_Rec_194947,Human_Splice_Rec_194961,Human_Splice_Rec_194975,Human_Splice_Rec_194987,Human_Splice_Rec_195001,Human_Splice_Rec_195013,Human_Splice_Rec_195027 110947 RMVar_ID_110947 Human_SNP_ID_805728573 m1A Human chr1 - 39883443 39883443 39883443 CTGCACGAGCAGTTCCCGTGGGCAGTGGGCTCAGGGGCCTGCAACGGACCCTACCTCTTGTAGTG CTGCACGAGCAGTTCCCGTGGGCAGTGGGCTCTGGGGCCTGCAACGGACCCTACCTCTTGTAGTG T A TRIT1 Ensembl:ENSG00000043514 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:39883378..39883446 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_355084,Human_RBP_ID_4073919,Human_RBP_ID_9271366,Human_RBP_ID_18415513,Human_RBP_ID_22430478,Human_RBP_ID_22488155 110948 RMVar_ID_110948 Human_SNP_ID_805736851 m1A Human chr1 - 77978898 77978890 77978898 AGGAGTTAACGACGCTTTCAAAGATGCACTGCAGAGAGCCCGGCAGGTAAGTGTGGACCGCGCGG AGGAGTTAACGACGCTTTCAAAGATGCACTGC________CGGCAGGTAAGTGTGGACCGCGCGG GGGCTCTCT G FUBP1 Ensembl:ENSG00000162613 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:77967637..77978961 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..40 33 MALY 1 - Human_RBP_ID_222739,Human_RBP_ID_743896,Human_RBP_ID_3322546,Human_RBP_ID_3933674,Human_RBP_ID_17338251,Human_RBP_ID_18414989,Human_RBP_ID_19035035,Human_RBP_ID_26309781 Human_Splice_Rec_88979,Human_Splice_Rec_89017,Human_Splice_Rec_89053,Human_Splice_Rec_89097 RMVar_hsa_circ_134177 110949 RMVar_ID_110949 Human_SNP_ID_805737754 m1A Human chr1 - 44214501 44214501 44214501 GAGGAGAAAATTGTTAGAGAAAACTAGGAGTTAGGGGCATGGCAGGTGAATCAGGGGCCAAAACC GAGGAGAAAATTGTTAGAGAAAACTAGGAGTTCGGGGCATGGCAGGTGAATCAGGGGCCAAAACC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:44214495..44214596 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast 110950 RMVar_ID_110950 Human_SNP_ID_805740453 m1A Human chr1 + 1490391 1490391 1490391 GCGGGAGCGCCTGGTGAGACTGCATTTTGACAACTGTGTTCTTAAGCCGGCCACAGAAGGAAAAC GCGGGAGCGCCTGGTGAGACTGCATTTTGACATCTGTGTTCTTAAGCCGGCCACAGAAGGAAAAC A T ATAD3B Ensembl:ENSG00000160072 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1490341..1490441 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_22044,Human_RBP_ID_9355318,Human_RBP_ID_18216080,Human_RBP_ID_18966836,Human_RBP_ID_22126423,Human_RBP_ID_22779559,Human_RBP_ID_22871131,Human_RBP_ID_27799537 Human_Splice_Rec_4151,Human_Splice_Rec_4177,Human_Splice_Rec_4203,Human_Splice_Rec_4227 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_125206,RMVar_hsa_circ_109226,RMVar_hsa_circ_128334,RMVar_hsa_circ_92990,RMVar_hsa_circ_128333,RMVar_hsa_circ_128340,RMVar_hsa_circ_99389,RMVar_hsa_circ_128342,RMVar_hsa_circ_128343,RMVar_hsa_circ_104837,RMVar_hsa_circ_128344,RMVar_hsa_circ_323510,RMVar_hsa_circ_128345,RMVar_hsa_circ_128346 110951 RMVar_ID_110951 Human_SNP_ID_805758272 m1A Human chr1 + 205121910 205121910 205121910 GCGGACTGTGGCCGCCCGGTCTCAGCTCCGGCAACAACACCTTCTCCCCGGCCGGCTTCAGCAAC GCGGACTGTGGCCGCCCGGTCTCAGCTCCGGCCACAACACCTTCTCCCCGGCCGGCTTCAGCAAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr1:205121857..205121934;chr1:205121800..205121925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 110952 RMVar_ID_110952 Human_SNP_ID_805758718 m1A Human chr1 + 1625322 1625322 1625322 GCCGGCGGAGCTGCAGCGCAGGGTGAGTGCTGACAGCCAGCCCTTCCAGCACGGGGACAAGGTCA GCCGGCGGAGCTGCAGCGCAGGGTGAGTGCTGGCAGCCAGCCCTTCCAGCACGGGGACAAGGTCA A G MIB2 Ensembl:ENSG00000197530 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:1625301..1625600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 14 brain Human_RBP_ID_3998921,Human_RBP_ID_9352456,Human_RBP_ID_9357873,Human_RBP_ID_18966844 Human_Splice_Rec_4462,Human_Splice_Rec_4498,Human_Splice_Rec_4532,Human_Splice_Rec_4568,Human_Splice_Rec_4604,Human_Splice_Rec_4638,Human_Splice_Rec_4674,Human_Splice_Rec_4720,Human_Splice_Rec_4762,Human_Splice_Rec_4806,Human_Splice_Rec_4840,Human_Splice_Rec_4870,Human_Splice_Rec_4902,Human_Splice_Rec_4934,Human_Splice_Rec_4960,Human_Splice_Rec_4964 110953 RMVar_ID_110953 Human_SNP_ID_805759550 m1A Human chr1 - 1313911 1313911 1313911 TGACTGGGCCGGTGGTCCCCAGGGAGCGCATGAACCTGAAGGTGCCCATCTACTTCTCCACGGGG TGACTGGGCCGGTGGTCCCCAGGGAGCGCATGGACCTGAAGGTGCCCATCTACTTCTCCACGGGG T C INTS11 Ensembl:ENSG00000127054 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:1313826..1313987 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 9 stomach Human_RBP_ID_3932469,Human_RBP_ID_19033542,Human_RBP_ID_22022552,Human_RBP_ID_22534689,Human_RBP_ID_22635317 Human_Splice_Rec_2802,Human_Splice_Rec_2836,Human_Splice_Rec_2870,Human_Splice_Rec_2896,Human_Splice_Rec_2920,Human_Splice_Rec_2948,Human_Splice_Rec_2980,Human_Splice_Rec_3008,Human_Splice_Rec_3032,Human_Splice_Rec_3102,Human_Splice_Rec_3130,Human_Splice_Rec_3154,Human_Splice_Rec_3186,Human_Splice_Rec_3220,Human_Splice_Rec_3276,Human_Splice_Rec_3304,Human_Splice_Rec_3316,Human_Splice_Rec_3324,Human_Splice_Rec_3334,Human_Splice_Rec_3348 RMVar_hsa_circ_7958,RMVar_hsa_circ_28672,RMVar_hsa_circ_117602,RMVar_hsa_circ_128309 110954 RMVar_ID_110954 Human_SNP_ID_805768769 m1A Human chr1 + 111449113 111449113 111449113 TGCCGTTCCATGCAGGCGGGCGCATTTGGGGGAAGATTCCACTCCCGGGCCGCCGGGGGCACTAG TGCCGTTCCATGCAGGCGGGCGCATTTGGGGGGAGATTCCACTCCCGGGCCGCCGGGGGCACTAG A G ATP5PB Ensembl:ENSG00000116459 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:111449062..111449179 32194978 MeRIP-seq:(Medium) rs992607622 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus 110955 RMVar_ID_110955 Human_SNP_ID_805769231 m1A Human chr1 + 111449529 111449529 111449529 GGGGTCACAGGGACGCTAAGATTGCTACCTGGACTTTCGTTGACCATGCTGTCCCGGGTGGTACT GGGGTCACAGGGACGCTAAGATTGCTACCTGGGCTTTCGTTGACCATGCTGTCCCGGGTGGTACT A G ATP5PB Ensembl:ENSG00000116459 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:111449451..111449622 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_321108,Human_RBP_ID_1408345,Human_RBP_ID_1722172,Human_RBP_ID_3982376,Human_RBP_ID_5311795,Human_RBP_ID_5483983,Human_RBP_ID_8281022,Human_RBP_ID_8953896,Human_RBP_ID_9320102,Human_RBP_ID_10520546,Human_RBP_ID_18547554,Human_RBP_ID_22427380,Human_RBP_ID_22779034,Human_RBP_ID_23322925,Human_RBP_ID_26798651,Human_RBP_ID_26837539,Human_RBP_ID_27164966 Human_Splice_Rec_109447,Human_Splice_Rec_109453,Human_Splice_Rec_109465,Human_Splice_Rec_109475,Human_Splice_Rec_109483 110956 RMVar_ID_110956 Human_SNP_ID_805770559 m1A Human chr1 - 10672210 10672210 10672210 TTATAGTGCGGAGGGGAGGGGGTGGCGGGGGGAGGGGGGAGAAGGTTAAACAGTATTTACAGCTC TTATAGTGCGGAGGGGAGGGGGTGGCGGGGGGGGGGGGGAGAAGGTTAAACAGTATTTACAGCTC T C CASZ1 Ensembl:ENSG00000130940 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:10672201..10672250 26863196 MeRIP-seq:(Medium) rs1202580993 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 110957 RMVar_ID_110957 Human_SNP_ID_805779621 m1A Human chr1 + 153661327 153661327 153661327 CAAATAACAGATGAGCCTATGGACTCAGTAGCACAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC CAAATAACAGATGAGCCTATGGACTCAGTAGCGCAAGTACTGTTCCCCAGCTGCCTTGTTTCAAC A G SNAPIN Ensembl:ENSG00000143553 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:153661281..153661432 32194978 MeRIP-seq:(Medium) rs16835489 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_326805,Human_RBP_ID_10583756,Human_RBP_ID_22127952 Human_miRNA_ID_623319 110958 RMVar_ID_110958 Human_SNP_ID_805791119 m1A Human chr1 - 1338371 1338371 1338371 TGGAGGGCTTCAAGGAGCGGCGGGAGGCCCGGAAGTACGCCAGCAGCTTGCTGAAGCACGGCTTC TGGAGGGCTTCAAGGAGCGGCGGGAGGCCCGGGAGTACGCCAGCAGCTTGCTGAAGCACGGCTTC T C DVL1 Ensembl:ENSG00000107404 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:1338251..1338512 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_3934863,Human_RBP_ID_18966777,Human_RBP_ID_22871120 Human_Splice_Rec_3552,Human_Splice_Rec_3580,Human_Splice_Rec_3602,Human_Splice_Rec_3618,Human_Splice_Rec_3630 RMVar_hsa_circ_26266,RMVar_hsa_circ_98157,RMVar_hsa_circ_120031,RMVar_hsa_circ_128315,RMVar_hsa_circ_128316,RMVar_hsa_circ_311238,RMVar_hsa_circ_317831,RMVar_hsa_circ_35273,RMVar_hsa_circ_35300,RMVar_hsa_circ_88949,RMVar_hsa_circ_128317,RMVar_hsa_circ_128318 110959 RMVar_ID_110959 Human_SNP_ID_805804274 m1A Human chr1 - 43975850 43975850 43975850 CTTCAAGGGGAATCCTCCCCCTGCCCTCCCTTACCATGCCACATCAAAGCGGAAGCCCAAATCAA CTTCAAGGGGAATCCTCCCCCTGCCCTCCCTTGCCATGCCACATCAAAGCGGAAGCCCAAATCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:43975714..43975864 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine 110960 RMVar_ID_110960 Human_SNP_ID_805816062 m1A Human chr1 - 1115830 1115830 1115830 CGCCGCCTCCCAACGAGCCTGGCCGCGGTCCTATGGGGGAAAGGCGCCCGGGCTGAGCGGGACGC CGCCGCCTCCCAACGAGCCTGGCCGCGGTCCTTTGGGGGAAAGGCGCCCGGGCTGAGCGGGACGC T A C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:1115828..1115965 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5336444 110961 RMVar_ID_110961 Human_SNP_ID_805844211 m1A Human chr1 - 43386066 43386066 43386066 CCAGGAGCTGGGACGATCCTTGCAGGAACCTCAGGATTACAGCAGGTGCAGATGGCAGGAGCTCC CCAGGAGCTGGGACGATCCTTGCAGGAACCTCGGGATTACAGCAGGTGCAGATGGCAGGAGCTCC T C MED8 Ensembl:ENSG00000159479 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:43385976..43386150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_1431828,Human_RBP_ID_1748522,Human_RBP_ID_5136718,Human_RBP_ID_17762576,Human_RBP_ID_22430530,Human_RBP_ID_26314089 Human_Splice_Rec_57737,Human_Splice_Rec_57749,Human_Splice_Rec_57763 110962 RMVar_ID_110962 Human_SNP_ID_805864910 m1A Human chr1 - 46303822 46303818 46303823 AGAGAAGAGGGCCGAGTGGATCGCCTTGCCTTACCTCCTCAGGATCTCCGGATTCGGTAAGCATC AGAGAAGAGGGCCGAGTGGATCGCCTTGCCT_____CCTCAGGATCTCCGGATTCGGTAAGCATC GAGGTA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:46303786..46303910 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..36 33 STAD 1 - 110963 RMVar_ID_110963 Human_SNP_ID_805869615 m1A Human chr1 + 92833598 92833597 92833599 CTCGGAAACGCTTGGTGATACAAGATAAAAATAAATACAACACACCCAAATACAGGATGATAGTT CTCGGAAACGCTTGGTGATACAAGATAAAAAT__ATACAACACACCCAAATACAGGATGATAGTT TAA T RPL5 Ensembl:ENSG00000122406 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:92833479..92833625 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_189788,Human_RBP_ID_365511,Human_RBP_ID_856828,Human_RBP_ID_1437084,Human_RBP_ID_1756987,Human_RBP_ID_2174501,Human_RBP_ID_3326274,Human_RBP_ID_8241041,Human_RBP_ID_8322040,Human_RBP_ID_8977331,Human_RBP_ID_17220607,Human_RBP_ID_17455818,Human_RBP_ID_17761128,Human_RBP_ID_18523453,Human_RBP_ID_18583354,Human_RBP_ID_22025975,Human_RBP_ID_22148430,Human_RBP_ID_22786539,Human_RBP_ID_22869993,Human_RBP_ID_23205231,Human_RBP_ID_23420943,Human_RBP_ID_24454788,Human_RBP_ID_26592367,Human_RBP_ID_26871845,Human_RBP_ID_27187746 Human_Splice_Rec_96176,Human_Splice_Rec_96177,Human_Splice_Rec_96190,Human_Splice_Rec_96191,Human_Splice_Rec_96204,Human_Splice_Rec_96205,Human_Splice_Rec_96214,Human_Splice_Rec_96215,Human_Splice_Rec_96224,Human_Splice_Rec_96225,Human_Splice_Rec_96230,Human_Splice_Rec_96231,Human_Splice_Rec_96237 RMVar_hsa_circ_51739,RMVar_hsa_circ_83856,RMVar_hsa_circ_104760,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_134578,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_53523,RMVar_hsa_circ_295226,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_134582 110964 RMVar_ID_110964 Human_SNP_ID_805877708 m1A Human chr1 + 9588868 9588868 9588868 GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCGCCTACCCCCCTG GCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTGCCCGCCTACCCGCCTACCCGCCTACCCCCCTG A G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr1:9588767..9588871 26863410 MeRIP-seq:(Medium) rs867507444 Functional Loss SNV ICGC 33..33 33 STAD 1 - 110965 RMVar_ID_110965 Human_SNP_ID_805881725 m1A Human chr1 - 229326967 229326965 229326968 AGTGAAAGATGTAGAAGATAAACCTGAACAACAAACCAGAACAAGAGAGACTGACAAATCACCCA AGTGAAAGATGTAGAAGATAAACCTGAACAA___ACCAGAACAAGAGAGACTGACAAATCACCCA TTTG T CCSAP Ensembl:ENSG00000154429 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:229326916..229327052 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 ESCA 1 - Human_RBP_ID_1739441,Human_RBP_ID_9357647,Human_RBP_ID_10827312,Human_RBP_ID_18410307 Human_Splice_Rec_197204,Human_Splice_Rec_197210,Human_Splice_Rec_197214 110966 RMVar_ID_110966 Human_SNP_ID_805883645 m1A Human chr1 - 220267082 220267082 220267082 AGAGCTTGAAATTGCAAATTTTGGGTGGTCAGAACATGCTCCATCTTCCAGGAGGACCACTCTCT AGAGCTTGAAATTGCAAATTTTGGGTGGTCAGTACATGCTCCATCTTCCAGGAGGACCACTCTCT T A AURKAP1,RAB3GAP2 Ensembl:ENSG00000213033,Ensembl:ENSG00000118873 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_5091391,Human_RBP_ID_17456679 110967 RMVar_ID_110967 Human_SNP_ID_805884101 m1A Human chr1 + 37552690 37552690 37552690 ACTGTTGAGTGGTGAGGACTTCGGTTTCTCTTACTGCGAGGAGACTTGCTTCTTCTCCCTGAGGC ACTGTTGAGTGGTGAGGACTTCGGTTTCTCTTCCTGCGAGGAGACTTGCTTCTTCTCCCTGAGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:37552589..37554046 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 110968 RMVar_ID_110968 Human_SNP_ID_805899664 m1A Human chr1 - 115976609 115976609 115976609 TCCTCCACCTCCATGGCGGGCCGCGCGCAGGAACCCCGCCACCCCACCGCCCTCTCAGGCGCTGC TCCTCCACCTCCATGGCGGGCCGCGCGCAGGAGCCCCGCCACCCCACCGCCCTCTCAGGCGCTGC T C LOC101928977,LOC101928977:2,LOC101928977:3,LOC101928977:4 RNACentral:URS00007E5084,RNACentral:URS0000D5C315,RNACentral:URS0000D5D731,RNACentral:URS0000D5DBEE lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:115976558..115976709 26863196 MeRIP-seq:(Medium) rs1366197876 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 110969 RMVar_ID_110969 Human_SNP_ID_805919646 m1A Human chr1 - 236554626 236554626 236554626 TACCCAGCATTTTATAAGTAAAGAGAGAGCAGAAGCCTTGATGATGCCTCTGGTGGATCAGGTAA TACCCAGCATTTTATAAGTAAAGAGAGAGCAGGAGCCTTGATGATGCCTCTGGTGGATCAGGTAA T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2275687 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 15 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_853321,Human_RBP_ID_9271868 Human_Splice_Rec_203335,Human_Splice_Rec_203421 GWAS_ID_10328,GWAS_ID_10329,GWAS_ID_10330,GWAS_ID_10331,GWAS_ID_10332,GWAS_ID_10333,GWAS_ID_10334,GWAS_ID_10335,GWAS_ID_10336,GWAS_ID_10337,GWAS_ID_10338,GWAS_ID_10339,GWAS_ID_10340,GWAS_ID_10341,GWAS_ID_10342,GWAS_ID_10343,GWAS_ID_10344,GWAS_ID_10345,GWAS_ID_10346,GWAS_ID_10347,GWAS_ID_10348,GWAS_ID_10349,GWAS_ID_10350,GWAS_ID_10351,GWAS_ID_10352,GWAS_ID_10353,GWAS_ID_10354,GWAS_ID_10355,GWAS_ID_10356,GWAS_ID_10357,GWAS_ID_10358,GWAS_ID_10359,GWAS_ID_10360,GWAS_ID_10361,GWAS_ID_10362,GWAS_ID_10363,GWAS_ID_10364,GWAS_ID_10365,GWAS_ID_10366,GWAS_ID_10367,GWAS_ID_10368,GWAS_ID_10369,GWAS_ID_10370,GWAS_ID_10371,GWAS_ID_10372,GWAS_ID_10373,GWAS_ID_10374,GWAS_ID_10375,GWAS_ID_10376,GWAS_ID_10377,GWAS_ID_10378,GWAS_ID_10379,GWAS_ID_10380,GWAS_ID_10381,GWAS_ID_10382,GWAS_ID_10383,GWAS_ID_10384,GWAS_ID_10385,GWAS_ID_10386,GWAS_ID_10387,GWAS_ID_10388,GWAS_ID_10389,GWAS_ID_10390,GWAS_ID_10391,GWAS_ID_10392,GWAS_ID_10393,GWAS_ID_10394,GWAS_ID_10395,GWAS_ID_10396,GWAS_ID_10397,GWAS_ID_10398,GWAS_ID_10399,GWAS_ID_10400,GWAS_ID_10401,GWAS_ID_10402,GWAS_ID_10403,GWAS_ID_10404,GWAS_ID_10405,GWAS_ID_10406,GWAS_ID_10407,GWAS_ID_10408,GWAS_ID_10409,GWAS_ID_10410,GWAS_ID_10411,GWAS_ID_10412,GWAS_ID_10413,GWAS_ID_10414,GWAS_ID_10415,GWAS_ID_10416,GWAS_ID_10417,GWAS_ID_10418,GWAS_ID_10419,GWAS_ID_10420,GWAS_ID_10421,GWAS_ID_10422,GWAS_ID_10423,GWAS_ID_10424,GWAS_ID_10425,GWAS_ID_10426,GWAS_ID_10427,GWAS_ID_10428,GWAS_ID_10429,GWAS_ID_10430,GWAS_ID_10431,GWAS_ID_10432,GWAS_ID_10433,GWAS_ID_10434,GWAS_ID_10435,GWAS_ID_10436,GWAS_ID_10437,GWAS_ID_10438,GWAS_ID_10439,GWAS_ID_10440,GWAS_ID_10441,GWAS_ID_10442,GWAS_ID_10443,GWAS_ID_10444,GWAS_ID_10445,GWAS_ID_10446,GWAS_ID_10447,GWAS_ID_10448,GWAS_ID_10449,GWAS_ID_10450,GWAS_ID_10451,GWAS_ID_10452,GWAS_ID_10453,GWAS_ID_10454,GWAS_ID_10455,GWAS_ID_10456,GWAS_ID_10457,GWAS_ID_10458,GWAS_ID_10459,GWAS_ID_10460,GWAS_ID_10461,GWAS_ID_10462,GWAS_ID_10463,GWAS_ID_10464,GWAS_ID_10465,GWAS_ID_10466,GWAS_ID_10467,GWAS_ID_10468,GWAS_ID_10469,GWAS_ID_10470,GWAS_ID_10471,GWAS_ID_10472,GWAS_ID_10473,GWAS_ID_10474,GWAS_ID_10475,GWAS_ID_10476,GWAS_ID_10477,GWAS_ID_10478,GWAS_ID_10479,GWAS_ID_10480,GWAS_ID_10481,GWAS_ID_10482,GWAS_ID_10483,GWAS_ID_10484,GWAS_ID_10485,GWAS_ID_10486,GWAS_ID_10487,GWAS_ID_10488,GWAS_ID_10489,GWAS_ID_10490,GWAS_ID_10491,GWAS_ID_10492,GWAS_ID_10493,GWAS_ID_10494,GWAS_ID_10495,GWAS_ID_10496,GWAS_ID_10497,GWAS_ID_10498,GWAS_ID_10499,GWAS_ID_10500,GWAS_ID_10501,GWAS_ID_10502,GWAS_ID_10503,GWAS_ID_10504,GWAS_ID_10505,GWAS_ID_10506,GWAS_ID_10507,GWAS_ID_10508,GWAS_ID_10509,GWAS_ID_10510,GWAS_ID_10511,GWAS_ID_10512,GWAS_ID_10513,GWAS_ID_10514,GWAS_ID_10515,GWAS_ID_10516,GWAS_ID_10517,GWAS_ID_10518,GWAS_ID_10519,GWAS_ID_10520,GWAS_ID_10521,GWAS_ID_10522,GWAS_ID_10523,GWAS_ID_10524,GWAS_ID_10525,GWAS_ID_10526,GWAS_ID_10527,GWAS_ID_10528,GWAS_ID_10529,GWAS_ID_10530,GWAS_ID_10531,GWAS_ID_10532,GWAS_ID_10533,GWAS_ID_10534,GWAS_ID_10535,GWAS_ID_10536,GWAS_ID_10537,GWAS_ID_10538,GWAS_ID_10539,GWAS_ID_10540,GWAS_ID_10541,GWAS_ID_10542,GWAS_ID_10543,GWAS_ID_10544,GWAS_ID_10545,GWAS_ID_10546,GWAS_ID_10547,GWAS_ID_10548,GWAS_ID_10549 RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_61188,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840 110970 RMVar_ID_110970 Human_SNP_ID_805928551 m1A Human chr1 - 30995178 30995178 30995178 ATGCAGACAGTGATGAAAACGACAAAGGTGAAAAGAAGAACAAGGGTACGTTTGATGGAGATAAG ATGCAGACAGTGATGAAAACGACAAAGGTGAAGAGAAGAACAAGGGTACGTTTGATGGAGATAAG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:30995076..31005883 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 14 kidney,skin,head and neck Human_RBP_ID_1745142,Human_RBP_ID_3935642,Human_RBP_ID_8754878,Human_RBP_ID_9443797,Human_RBP_ID_10928282,Human_RBP_ID_17646324,Human_RBP_ID_18571716,Human_RBP_ID_22784206,Human_RBP_ID_23386766 Human_Splice_Rec_39958,Human_Splice_Rec_40000,Human_Splice_Rec_40042,Human_Splice_Rec_40082,Human_Splice_Rec_40156,Human_Splice_Rec_40198,Human_Splice_Rec_40236,Human_Splice_Rec_40354,Human_Splice_Rec_40368 RMVar_hsa_circ_83915,RMVar_hsa_circ_372758,RMVar_hsa_circ_130987,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_67706,RMVar_hsa_circ_131001,RMVar_hsa_circ_111157,RMVar_hsa_circ_45672,RMVar_hsa_circ_131002,RMVar_hsa_circ_296277,RMVar_hsa_circ_71922,RMVar_hsa_circ_53855,RMVar_hsa_circ_131013,RMVar_hsa_circ_116197,RMVar_hsa_circ_346734,RMVar_hsa_circ_307848,RMVar_hsa_circ_131014,RMVar_hsa_circ_46483,RMVar_hsa_circ_131019,RMVar_hsa_circ_273051,RMVar_hsa_circ_303728,RMVar_hsa_circ_82449,RMVar_hsa_circ_118532,RMVar_hsa_circ_131026,RMVar_hsa_circ_60205,RMVar_hsa_circ_47681,RMVar_hsa_circ_131027,RMVar_hsa_circ_131024,RMVar_hsa_circ_131025,RMVar_hsa_circ_354236,RMVar_hsa_circ_131030,RMVar_hsa_circ_116734,RMVar_hsa_circ_131029,RMVar_hsa_circ_275323,RMVar_hsa_circ_355888,RMVar_hsa_circ_379111,RMVar_hsa_circ_281339,RMVar_hsa_circ_274609,RMVar_hsa_circ_131032,RMVar_hsa_circ_131034,RMVar_hsa_circ_131035,RMVar_hsa_circ_131033,RMVar_hsa_circ_131031,RMVar_hsa_circ_64658,RMVar_hsa_circ_64820 110971 RMVar_ID_110971 Human_SNP_ID_805933093 m1A Human chr1 + 234607676 234607676 234607676 CTGGGCCGCTTCAGGCGGTGTGGTCCGGTTGGAATGAGGTGAGGCAGTGGGTGGTGGCGGAGACA CTGGGCCGCTTCAGGCGGTGTGGTCCGGTTGGGATGAGGTGAGGCAGTGGGTGGTGGCGGAGACA A G AL160408.2 Ensembl:ENSG00000228830 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:234607651..234607675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach 110972 RMVar_ID_110972 Human_SNP_ID_805934978 m1A Human chr1 + 228495438 228495438 228495438 AGGGCAAAGAGGGCCCTAGGAGAAGATTCCAGAGCCTGGCCAGAGTTTGGCCAAGTAGAGAATCT AGGGCAAAGAGGGCCCTAGGAGAAGATTCCAGGGCCTGGCCAGAGTTTGGCCAAGTAGAGAATCT A G RNF187 Ensembl:ENSG00000168159 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10916331 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_10324,GWAS_ID_10325,GWAS_ID_10326 110973 RMVar_ID_110973 Human_SNP_ID_805936163 m1A Human chr1 + 110339499 110339499 110339499 CGCTGTGTGAAACGAGCGCGGGGCGGCGGGTTACTCAGCTCCGCGGAGACGACCTCCGACGACCC CGCTGTGTGAAACGAGCGCGGGGCGGCGGGTTGCTCAGCTCCGCGGAGACGACCTCCGACGACCC A G RBM15 Ensembl:ENSG00000162775 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:110339449..110339599 26863196 MeRIP-seq:(Medium) rs1557890295 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_224477,Human_RBP_ID_3981604 110974 RMVar_ID_110974 Human_SNP_ID_805938738 m1A Human chr1 + 154966321 154966321 154966321 CCCCAGCCCGCCTCCATCCAAGCAACTTACCAATGTAGCTCCCAAGTGGCTGGGGGTCTGGGCAT CCCCAGCCCGCCTCCATCCAAGCAACTTACCAGTGTAGCTCCCAAGTGGCTGGGGGTCTGGGCAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr1:154966301..154966350 26863196 MeRIP-seq:(Medium) rs77859168 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate 110975 RMVar_ID_110975 Human_SNP_ID_805942205 m1A Human chr1 - 16589030 16589030 16589030 CAATATAAAGTCCTGGTTCACTCTCAGGAACGAGAGCTGACCCAGTTAAGGGAGAAGTTACGGGA CAATATAAAGTCCTGGTTCACTCTCAGGAACGGGAGCTGACCCAGTTAAGGGAGAAGTTACGGGA T C NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs201237274 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 2 head and neck Human_Splice_Rec_22506,Human_Splice_Rec_22560 RMVar_hsa_circ_55378,RMVar_hsa_circ_67715,RMVar_hsa_circ_122744,RMVar_hsa_circ_125516,RMVar_hsa_circ_129552,RMVar_hsa_circ_129553 110976 RMVar_ID_110976 Human_SNP_ID_805946763 m1A Human chr1 - 23796621 23796621 23796621 CAGGCAGAGCGGCCCAGAGGCGTGGTCAGTCCAGCCCGCTCCATAAACCCTGTTCTCCGTGGGCC CAGGCAGAGCGGCCCAGAGGCGTGGTCAGTCCGGCCCGCTCCATAAACCCTGTTCTCCGTGGGCC T C GALE Ensembl:ENSG00000117308 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:23796608..23796699 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_746320,Human_RBP_ID_5331274,Human_RBP_ID_19042905,Human_RBP_ID_22413995,Human_RBP_ID_22633163 110977 RMVar_ID_110977 Human_SNP_ID_805963863 m1A Human chr1 + 25817043 25817043 25817043 TTAAGGTCTTGAAGTCAGGCTGCCCCCTCCCCAGCCCCCAGTTCTCTCCCCACCCCCTCACCCCA TTAAGGTCTTGAAGTCAGGCTGCCCCCTCCCCCGCCCCCAGTTCTCTCCCCACCCCCTCACCCCA A C SELENON,AL020996.2 Ensembl:ENSG00000162430,Ensembl:ENSG00000255054 Protein coding,Protein coding 3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25816997..25817142 26863196 MeRIP-seq:(Medium) rs1372816667 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_350006,Human_RBP_ID_5136133,Human_RBP_ID_5801152,Human_RBP_ID_10899821,Human_RBP_ID_17072299,Human_RBP_ID_17217506 Human_miRNA_ID_841305,Human_miRNA_ID_1355181,Human_miRNA_ID_2071751,Human_miRNA_ID_2073431,Human_miRNA_ID_2135309,Human_miRNA_ID_2365679,Human_miRNA_ID_2365680,Human_miRNA_ID_2664111,Human_miRNA_ID_2682635,Human_miRNA_ID_2724593,Human_miRNA_ID_3013485,Human_miRNA_ID_3063592 RMVar_hsa_circ_114934,RMVar_hsa_circ_130585,RMVar_hsa_circ_85638,RMVar_hsa_circ_130591,RMVar_hsa_circ_103238,RMVar_hsa_circ_130595 110978 RMVar_ID_110978 Human_SNP_ID_805972732 m1A Human chr1 + 9269047 9269046 9269047 TGGGGCTCCCTTAGAACTTACTCCACTGATTTAAAAAAAAAAAACTGCCTGGCAGCATCTCAGTG TGGGGCTCCCTTAGAACTTACTCCACTGATTT_AAAAAAAAAAACTGCCTGGCAGCATCTCAGTG TA T H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..33 33 CHOL 2 - Human_RBP_ID_27401788 Human_miRNA_ID_2278672,Human_miRNA_ID_2458734,Human_miRNA_ID_2638982 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 110979 RMVar_ID_110979 Human_SNP_ID_805973812 m1A Human chr1 - 45340249 45340249 45340249 ACTGCGCCATCGTCACTGTCGGCGGCCATGACACCGCTCGTCTCCCGCCTGAGTCGTCTGTGGGT ACTGCGCCATCGTCACTGTCGGCGGCCATGACGCCGCTCGTCTCCCGCCTGAGTCGTCTGTGGGT T C MUTYH,AL451136.1 Ensembl:ENSG00000132781,Ensembl:ENSG00000288208 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:45340198..45340392 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_62977,Human_Splice_Rec_63161,Human_Splice_Rec_63189,Human_Splice_Rec_63217,Human_Splice_Rec_63245,Human_Splice_Rec_63273,Human_Splice_Rec_63311,Human_Splice_Rec_63343,Human_Splice_Rec_63529,Human_Splice_Rec_63569,Human_Splice_Rec_63605,Human_Splice_Rec_63631,Human_Splice_Rec_63659,Human_Splice_Rec_63671,Human_Splice_Rec_63679,Human_Splice_Rec_63693,Human_Splice_Rec_63701 110980 RMVar_ID_110980 Human_SNP_ID_805980559 m1A Human chr1 + 181089645 181089645 181089645 CCCGCTCAAGAAGCCCCGCCGGAACTTAGAGCAGCCGCCGAGTGGAGGAGAGGACGACGACGCGG CCCGCTCAAGAAGCCCCGCCGGAACTTAGAGCCGCCGCCGAGTGGAGGAGAGGACGACGACGCGG A C IER5 Ensembl:ENSG00000162783 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:181088761..181089908 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_10686913,Human_RBP_ID_22486540 110981 RMVar_ID_110981 Human_SNP_ID_805985648 m1A Human chr1 + 21573678 21573678 21573678 CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCAGGGGACATGCAGTACGAGCTGAACAGGAACAA CTCCTGGCGTCCTCCTCAGGTCTCTTCGAGCCGGGGGACATGCAGTACGAGCTGAACAGGAACAA A G ALPL Ensembl:ENSG00000162551 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3200255 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_Splice_Rec_27804,Human_Splice_Rec_27822,Human_Splice_Rec_27842,Human_Splice_Rec_27864 Clinvar_Rec_237,Clinvar_Rec_238 GWAS_ID_7750,GWAS_ID_7751,GWAS_ID_7752,GWAS_ID_7753,GWAS_ID_7754 RMVar_hsa_circ_12620 110982 RMVar_ID_110982 Human_SNP_ID_805994856 m1A Human chr1 + 32332192 32332191 32332193 CCGCAAGAACTCTTCCAACTTCAAAAAAGCCAAGAGAGTCAAAACAGAGGATGAAAAAGAGAAAG CCGCAAGAACTCTTCCAACTTCAAAAAAGCCA__AGAGTCAAAACAGAGGATGAAAAAGAGAAAG AAG A HDAC1 Ensembl:ENSG00000116478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:32332141..32332261 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_18128,Human_RBP_ID_191360,Human_RBP_ID_859562,Human_RBP_ID_2143434,Human_RBP_ID_3935677,Human_RBP_ID_5518769,Human_RBP_ID_8227977,Human_RBP_ID_9355936,Human_RBP_ID_17646330,Human_RBP_ID_18965168,Human_RBP_ID_22870800,Human_RBP_ID_24541447,Human_RBP_ID_26310756,Human_RBP_ID_26862530,Human_RBP_ID_27797738 Human_Splice_Rec_43309,Human_Splice_Rec_43379,Human_Splice_Rec_43389 RMVar_hsa_circ_116794,RMVar_hsa_circ_131229,RMVar_hsa_circ_110997,RMVar_hsa_circ_91934,RMVar_hsa_circ_131231,RMVar_hsa_circ_131233,RMVar_hsa_circ_81817,RMVar_hsa_circ_109004,RMVar_hsa_circ_131234,RMVar_hsa_circ_116341,RMVar_hsa_circ_131235,RMVar_hsa_circ_131237,RMVar_hsa_circ_80184,RMVar_hsa_circ_101227,RMVar_hsa_circ_90365,RMVar_hsa_circ_131238,RMVar_hsa_circ_131239,RMVar_hsa_circ_131240 110983 RMVar_ID_110983 Human_SNP_ID_805997139 m1A Human chr1 - 6356393 6356384 6356393 GCTGAGGGTGCTGGGCAGGGCTGAGGGTGCTGAGGGTGCTGCCGCTGCTGCCTCGGGGCTCCCCT GCTGAGGGTGCTGGGCAGGGCTGAGGGTGCTG_________CCGCTGCTGCCTCGGGGCTCCCCT GCAGCACCCT G ACOT7 Ensembl:ENSG00000097021 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:6356391..6356637 26863196 MeRIP-seq:(Medium) rs796908651 Functional Loss DEL ICGC 33..41 33 MALY 1 - RMVar_hsa_circ_112671,RMVar_hsa_circ_106361,RMVar_hsa_circ_128631,RMVar_hsa_circ_128630 110984 RMVar_ID_110984 Human_SNP_ID_806011949 m1A Human chr1 + 24535182 24535182 24535182 TCTGTGAAAGTGAAACTGAAGAGGAAGAAGAGACAAAAAACCCCAAACAGAAAATTGCCCAGACG TCTGTGAAAGTGAAACTGAAGAGGAAGAAGAGTCAAAAAACCCCAAACAGAAAATTGCCCAGACG A T RCAN3 Ensembl:ENSG00000117602 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:24535132..24535251 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_myelomonocytic_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_18523100,Human_RBP_ID_18569970 Human_Splice_Rec_31538,Human_Splice_Rec_31544,Human_Splice_Rec_31552,Human_Splice_Rec_31558,Human_Splice_Rec_31564,Human_Splice_Rec_31572,Human_Splice_Rec_31580,Human_Splice_Rec_31584,Human_Splice_Rec_31588,Human_Splice_Rec_31590,Human_Splice_Rec_31592 RMVar_hsa_circ_266968 110985 RMVar_ID_110985 Human_SNP_ID_806027044 m1A Human chr1 + 150159255 150159255 150159255 CCTGGTAGCAAGGAAACTGGAGGAGACTCAGGAGCTTCTGGCAGAGGTTCAGGGACTGGGAGATG CCTGGTAGCAAGGAAACTGGAGGAGACTCAGGGGCTTCTGGCAGAGGTTCAGGGACTGGGAGATG A G PLEKHO1 Ensembl:ENSG00000023902 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:150159151..150159475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8284466,Human_RBP_ID_8734450,Human_RBP_ID_23330637 110986 RMVar_ID_110986 Human_SNP_ID_806027697 m1A Human chr1 + 92833614 92833614 92833614 GATACAAGATAAAAATAAATACAACACACCCAAATACAGGATGATAGTTCGTGTGACAAACAGAG GATACAAGATAAAAATAAATACAACACACCCACATACAGGATGATAGTTCGTGTGACAAACAGAG A C RPL5 Ensembl:ENSG00000122406 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:92833478..92833646 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_RBP_ID_365511,Human_RBP_ID_1437084,Human_RBP_ID_1756987,Human_RBP_ID_2174502,Human_RBP_ID_3326274,Human_RBP_ID_4070262,Human_RBP_ID_5162311,Human_RBP_ID_5883208,Human_RBP_ID_8322040,Human_RBP_ID_8977331,Human_RBP_ID_11156308,Human_RBP_ID_17220607,Human_RBP_ID_17679148,Human_RBP_ID_17761128,Human_RBP_ID_18523454,Human_RBP_ID_18583354,Human_RBP_ID_22022372,Human_RBP_ID_22148430,Human_RBP_ID_22488979,Human_RBP_ID_22869993,Human_RBP_ID_23420946,Human_RBP_ID_26391300,Human_RBP_ID_26592367,Human_RBP_ID_26798573,Human_RBP_ID_26871845,Human_RBP_ID_27600780 Human_Splice_Rec_96176,Human_Splice_Rec_96177,Human_Splice_Rec_96190,Human_Splice_Rec_96191,Human_Splice_Rec_96204,Human_Splice_Rec_96205,Human_Splice_Rec_96214,Human_Splice_Rec_96215,Human_Splice_Rec_96224,Human_Splice_Rec_96225,Human_Splice_Rec_96230,Human_Splice_Rec_96231,Human_Splice_Rec_96237 Human_miRNA_ID_1398473 RMVar_hsa_circ_51739,RMVar_hsa_circ_83856,RMVar_hsa_circ_104760,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_134578,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_53523,RMVar_hsa_circ_295226,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_134582 110987 RMVar_ID_110987 Human_SNP_ID_806035609 m1A Human chr1 + 33013341 33013341 33013341 TGAGTGGGGTGGTTTGAGTGTGGTAGGCTTGCAGGCGGATTTTCAAGGCCTTTTCATTATCATCT TGAGTGGGGTGGTTTGAGTGTGGTAGGCTTGCGGGCGGATTTTCAAGGCCTTTTCATTATCATCT A G AL020995.1 Ensembl:ENSG00000236065 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr1:33013244..33013407 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 110988 RMVar_ID_110988 Human_SNP_ID_806042470 m1A Human chr1 + 67686391 67686391 67686391 TAACGTGGTGTTGTGCCTGCTGGCGGCGGACGAGGACGACGACAGAGATGTGGCTCTGCAGATCC TAACGTGGTGTTGTGCCTGCTGGCGGCGGACGTGGACGACGACAGAGATGTGGCTCTGCAGATCC A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 110989 RMVar_ID_110989 Human_SNP_ID_806053313 m1A Human chr1 + 25805243 25805243 25805243 TAGAAGCCCGATTCCAGCCTCTGCTCCCGGAGACCATGACCAAGAGCAAAGATGGCTTCCTAGGG TAGAAGCCCGATTCCAGCCTCTGCTCCCGGAGGCCATGACCAAGAGCAAAGATGGCTTCCTAGGG A G SELENON Ensembl:ENSG00000162430 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25805195..25805324 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_32669,Human_Splice_Rec_32695,Human_Splice_Rec_32717 RMVar_hsa_circ_6205,RMVar_hsa_circ_35596,RMVar_hsa_circ_105872,RMVar_hsa_circ_114934,RMVar_hsa_circ_364975,RMVar_hsa_circ_130585,RMVar_hsa_circ_322366,RMVar_hsa_circ_49070,RMVar_hsa_circ_17014,RMVar_hsa_circ_18474,RMVar_hsa_circ_92812,RMVar_hsa_circ_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586,RMVar_hsa_circ_44592,RMVar_hsa_circ_130588 110990 RMVar_ID_110990 Human_SNP_ID_806058782 m1A Human chr1 + 223712848 223712848 223712848 GCTTCAAGGAGTTGGGGCCCTACTCCAGCAAAACCCGGGGCATCGAGTGGAAGCGCCCCACGGTA GCTTCAAGGAGTTGGGGCCCTACTCCAGCAAAGCCCGGGGCATCGAGTGGAAGCGCCCCACGGTA A G CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:223712801..223712900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_222782,Human_RBP_ID_342614,Human_RBP_ID_9270655 Human_Splice_Rec_190627 RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 110991 RMVar_ID_110991 Human_SNP_ID_806072019 m1A Human chr1 - 41623780 41623780 41623780 TCAGCTTGCCAAACCAGGGCTGGCACAGGAGGAGGAGGGCCTGGAGCATGGGCCGTGTTTGTGAG TCAGCTTGCCAAACCAGGGCTGGCACAGGAGGGGGAGGGCCTGGAGCATGGGCCGTGTTTGTGAG T C HIVEP3,AC119676.1 Ensembl:ENSG00000127124,Ensembl:ENSG00000284895 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:41623729..41623818 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_67575 110992 RMVar_ID_110992 Human_SNP_ID_806078687 m1A Human chr1 + 173477372 173477372 173477372 TTCGCCAGAACCAACCGGTTGCTTGCTGTCCCAGCGGCGCCCCCTCATCACCGTCGCCATGCCCG TTCGCCAGAACCAACCGGTTGCTTGCTGTCCCGGCGGCGCCCCCTCATCACCGTCGCCATGCCCG A G PRDX6 Ensembl:ENSG00000117592 Protein coding exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr1:173477326..173477565;chr1:173477301..173477621;chr1:173477301..173477572;chr1:173477301..173477631 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_223775,Human_RBP_ID_333193,Human_RBP_ID_803319,Human_RBP_ID_1345500,Human_RBP_ID_3287033,Human_RBP_ID_4008652,Human_RBP_ID_5433211,Human_RBP_ID_5456636,Human_RBP_ID_8290600,Human_RBP_ID_17456345,Human_RBP_ID_22026090,Human_RBP_ID_26799180,Human_RBP_ID_26847159,Human_RBP_ID_27171773 RMVar_hsa_circ_110680,RMVar_hsa_circ_137631 110993 RMVar_ID_110993 Human_SNP_ID_806081505 m1A Human chr1 - 19345237 19345236 19345237 GTTTCTGTCTTTTGCAGATGGAGAAGGATGAAACTGTGAGTGACTGCTCCCCACACATAGCCAAC GTTTCTGTCTTTTGCAGATGGAGAAGGATGAA_CTGTGAGTGACTGCTCCCCACACATAGCCAAC GT G CAPZB Ensembl:ENSG00000077549 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:19345145..19345302 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_10713598,Human_RBP_ID_22426951,Human_RBP_ID_22633029,Human_RBP_ID_22734625,Human_RBP_ID_23353951,Human_RBP_ID_27392227 Human_Splice_Rec_25330,Human_Splice_Rec_25331,Human_Splice_Rec_25348,Human_Splice_Rec_25349,Human_Splice_Rec_25362,Human_Splice_Rec_25363,Human_Splice_Rec_25369,Human_Splice_Rec_25386,Human_Splice_Rec_25387,Human_Splice_Rec_25402,Human_Splice_Rec_25416,Human_Splice_Rec_25432,Human_Splice_Rec_25433,Human_Splice_Rec_25446,Human_Splice_Rec_25447,Human_Splice_Rec_25462,Human_Splice_Rec_25463,Human_Splice_Rec_25474,Human_Splice_Rec_25475 Human_miRNA_ID_2284037,Human_miRNA_ID_2287035,Human_miRNA_ID_2365657,Human_miRNA_ID_2995789 RMVar_hsa_circ_61484,RMVar_hsa_circ_265503,RMVar_hsa_circ_296140,RMVar_hsa_circ_368127,RMVar_hsa_circ_72794,RMVar_hsa_circ_129825,RMVar_hsa_circ_367286 110994 RMVar_ID_110994 Human_SNP_ID_806091805 m1A Human chr1 - 43172465 43172465 43172465 CTGCTACCAGCTCCTTCTGGCGACCCCCAGGTACCCCCTCCCACCTTTCGTTTCTCTCTGGGTCA CTGCTACCAGCTCCTTCTGGCGACCCCCAGGTGCCCCCTCCCACCTTTCGTTTCTCTCTGGGTCA T C EBNA1BP2 Ensembl:ENSG00000117395 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:43172420..43172520 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THYM 1 - 110995 RMVar_ID_110995 Human_SNP_ID_806101221 m1A Human chr1 - 204411227 204411227 204411227 TTCCTCTGCCCAGCCCGAGACTCGGGTCAGTTACTGGACGAAACTGCTCTCCCAGCTCCTTGCGC TTCCTCTGCCCAGCCCGAGACTCGGGTCAGTTGCTGGACGAAACTGCTCTCCCAGCTCCTTGCGC T C PPP1R15B Ensembl:ENSG00000158615 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr1:204411176..204411394;chr1:204411176..204411250 26863196 MeRIP-seq:(Medium) rs751708347 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 1 head and neck Human_RBP_ID_272229,Human_RBP_ID_338588,Human_RBP_ID_1419257,Human_RBP_ID_4087449,Human_RBP_ID_8295599,Human_RBP_ID_8741175,Human_RBP_ID_10735742,Human_RBP_ID_17338614,Human_RBP_ID_22024133,Human_RBP_ID_23357312,Human_RBP_ID_27174066,Human_RBP_ID_27392867,Human_RBP_ID_27584954 110996 RMVar_ID_110996 Human_SNP_ID_806104412 m1A Human chr1 - 247329536 247329536 247329536 CCCTGTGCCCCCGAGTCTTGGCTCCGAAGGAAAGTGAGGAGCCCAGGAAAATGAGGAGCCCACCT CCCTGTGCCCCCGAGTCTTGGCTCCGAAGGAATGTGAGGAGCCCAGGAAAATGAGGAGCCCACCT T A ZNF496 Ensembl:ENSG00000162714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:247329485..247329639 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_9357768 Human_Splice_Rec_208726,Human_Splice_Rec_208758,Human_Splice_Rec_208766 RMVar_hsa_circ_73657,RMVar_hsa_circ_351460 110997 RMVar_ID_110997 Human_SNP_ID_806107153 m1A Human chr1 - 16206995 16206995 16206995 CGCTGTGGCAGGATATCCCCGACGTACGCGGCAGCGGCGTCCTGGCCACGCTGAGCCTGCGGGAC CGCTGTGGCAGGATATCCCCGACGTACGCGGCTGCGGCGTCCTGGCCACGCTGAGCCTGCGGGAC T A ARHGEF19 Ensembl:ENSG00000142632 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:16206871..16206997 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_Splice_Rec_21971,Human_Splice_Rec_22001,Human_Splice_Rec_22039 RMVar_hsa_circ_94790,RMVar_hsa_circ_98742,RMVar_hsa_circ_90184,RMVar_hsa_circ_129523,RMVar_hsa_circ_129524,RMVar_hsa_circ_129525,RMVar_hsa_circ_129526,RMVar_hsa_circ_97587 110998 RMVar_ID_110998 Human_SNP_ID_806107671 m1A Human chr1 - 156134764 156134764 156134764 GTTGGAGGAAGGACACAGAAACCAAAATCAGAATTAGTTCCTGGGAGGCCAAGACCCAGGGGCGG GTTGGAGGAAGGACACAGAAACCAAAATCAGAGTTAGTTCCTGGGAGGCCAAGACCCAGGGGCGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr1:156134758..156134911 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 110999 RMVar_ID_110999 Human_SNP_ID_806107672 m1A Human chr1 - 154170467 154170467 154170467 TGGTTCTGACTAATTTCATATTTCCCCCAGGCAGAGACCCGTGCTGAGTTTGCTGAGAGATCGGT TGGTTCTGACTAATTTCATATTTCCCCCAGGCGGAGACCCGTGCTGAGTTTGCTGAGAGATCGGT T C TPM3 Ensembl:ENSG00000143549 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr1:154170401..154170475 32194978 MeRIP-seq:(Medium) rs373670110 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 13 lung Human_RBP_ID_222251,Human_RBP_ID_1064554,Human_RBP_ID_3995735,Human_RBP_ID_9356872,Human_RBP_ID_22634345,Human_RBP_ID_22735160,Human_RBP_ID_26311839,Human_RBP_ID_27800819 Human_Splice_Rec_133478,Human_Splice_Rec_133479,Human_Splice_Rec_133492,Human_Splice_Rec_133493,Human_Splice_Rec_133498,Human_Splice_Rec_133499,Human_Splice_Rec_133506,Human_Splice_Rec_133507,Human_Splice_Rec_133520,Human_Splice_Rec_133521,Human_Splice_Rec_133534,Human_Splice_Rec_133535,Human_Splice_Rec_133548,Human_Splice_Rec_133549,Human_Splice_Rec_133560,Human_Splice_Rec_133561,Human_Splice_Rec_133566,Human_Splice_Rec_133567,Human_Splice_Rec_133584,Human_Splice_Rec_133585,Human_Splice_Rec_133598,Human_Splice_Rec_133599,Human_Splice_Rec_133612,Human_Splice_Rec_133613,Human_Splice_Rec_133628,Human_Splice_Rec_133629,Human_Splice_Rec_133634,Human_Splice_Rec_133635,Human_Splice_Rec_133648,Human_Splice_Rec_133649,Human_Splice_Rec_133662,Human_Splice_Rec_133663,Human_Splice_Rec_133676,Human_Splice_Rec_133677,Human_Splice_Rec_133692,Human_Splice_Rec_133693,Human_Splice_Rec_133710,Human_Splice_Rec_133711,Human_Splice_Rec_133716,Human_Splice_Rec_133724 RMVar_hsa_circ_136356,RMVar_hsa_circ_285478,RMVar_hsa_circ_369627,RMVar_hsa_circ_279851,RMVar_hsa_circ_320725 111000 RMVar_ID_111000 Human_SNP_ID_806117191 m1A Human chr1 + 155978084 155978084 155978084 CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCAAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG CGCTCCGTCCCTTACCGGAGCAACTTTCTTTCGAGCGGCCTAAAGCACTCGGTCCCGCCGGCTTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155978082..155978160 26863196 MeRIP-seq:(Medium) rs928596 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,liver hepatocellular_carcinoma 5 liver GWAS_ID_12214,GWAS_ID_12215,GWAS_ID_12216,GWAS_ID_12217 111001 RMVar_ID_111001 Human_SNP_ID_806132879 m1A Human chr1 - 16619912 16619912 16619912 CCGGCGGAAGGCTGAGAAGGAACAGCTGAGTGAGGAGATTGCTGCCCTGCAGCAGGAGCATGACG CCGGCGGAAGGCTGAGAAGGAACAGCTGAGTGCGGAGATTGCTGCCCTGCAGCAGGAGCATGACG T G CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:16619095..16620036 26863196 MeRIP-seq:(Medium) rs10796418 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_332624,Human_RBP_ID_5538484,Human_RBP_ID_18415924 Human_Splice_Rec_22653,Human_Splice_Rec_22663,Human_Splice_Rec_22675,Human_Splice_Rec_22731 RMVar_hsa_circ_56321 111002 RMVar_ID_111002 Human_SNP_ID_806138027 m1A Human chr1 - 16545943 16545943 16545943 CACGCGGGAGACCCGGGTTCAATTCCCGGCCAATGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT CACGCGGGAGACCCGGGTTCAATTCCCGGCCAGTGCAAGAGGGTCTTTTTCACCCCGCTGTTGCT T C tRNA-Gly-CCC-1-1 RNACentral:URS00004BF687 tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:16545899..16546003 26863196 MeRIP-seq:(Medium) rs188712584 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_972707,Human_RBP_ID_1232906,Human_RBP_ID_1415120,Human_RBP_ID_1728729,Human_RBP_ID_5252964,Human_RBP_ID_5273284,Human_RBP_ID_5710283,Human_RBP_ID_8289877,Human_RBP_ID_9556180,Human_RBP_ID_10647175,Human_RBP_ID_17072885,Human_RBP_ID_17730443,Human_RBP_ID_18555621,Human_RBP_ID_19446038,Human_RBP_ID_21999636,Human_RBP_ID_22130935,Human_RBP_ID_22786833,Human_RBP_ID_22849846,Human_RBP_ID_23112693,Human_RBP_ID_23121724,Human_RBP_ID_23343520,Human_RBP_ID_24754056,Human_RBP_ID_26579402,Human_RBP_ID_26846451,Human_RBP_ID_27171396 111003 RMVar_ID_111003 Human_SNP_ID_806151404 m1A Human chr1 + 46248096 46248096 46248096 CTCCCTTCACCCGGACTGGGACCATCATCCCCACTCCACTCCGCCCAGTCTGGGACTCCACCTGC CTCCCTTCACCCGGACTGGGACCATCATCCCCCCTCCACTCCGCCCAGTCTGGGACTCCACCTGC A C RAD54L Ensembl:ENSG00000085999 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr1:46248072..46248176 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_1154895,Human_RBP_ID_4056546,Human_RBP_ID_5125260,Human_RBP_ID_5312523,Human_RBP_ID_5414074,Human_RBP_ID_5434209,Human_RBP_ID_5486480,Human_RBP_ID_17071157,Human_RBP_ID_18928348,Human_RBP_ID_19372073,Human_RBP_ID_22865019,Human_RBP_ID_24766357,Human_RBP_ID_27184180,Human_RBP_ID_27402853 111004 RMVar_ID_111004 Human_SNP_ID_806155777 m1A Human chr1 - 39563604 39563604 39563604 ATCCTGCCATACAGCCTCTGCAGGTGAGGTTCACCAGACAGAATGCTTAAAAGGATTTCCCCCAT ATCCTGCCATACAGCCTCTGCAGGTGAGGTTCGCCAGACAGAATGCTTAAAAGGATTTCCCCCAT T C PABPC4 Ensembl:ENSG00000090621 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr1:39563601..39563727 32194978 MeRIP-seq:(Medium) rs757048030 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_2183221,Human_RBP_ID_18968062,Human_RBP_ID_19034619 RMVar_hsa_circ_75969,RMVar_hsa_circ_116806,RMVar_hsa_circ_113357,RMVar_hsa_circ_31319,RMVar_hsa_circ_131960,RMVar_hsa_circ_131961,RMVar_hsa_circ_131959,RMVar_hsa_circ_26878 111005 RMVar_ID_111005 Human_SNP_ID_806160763 m1A Human chr1 - 173688609 173688605 173688609 AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAGAGAGGAAGAGGCAGAGAGAGAGAGAGGAAGCGG AGGCAGAAAGAGGAAGAGGCGGAGAGAGAGAG____GAAGAGGCAGAGAGAGAGAGAGGAAGCGG CCTCT C lnc-ANKRD45-3 RNACentral:URS0000D57E23 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:173688559..173688642 26863196 MeRIP-seq:(Medium) rs771296140 Functional Loss DEL ICGC 33..36 33 BRCA 1 - 111006 RMVar_ID_111006 Human_SNP_ID_806176128 m1A Human chr1 + 205187603 205187603 205187603 GAGCGCCAGGCTGACCCGAGTCTGAGTCCCATAGGTGAAGCGGAGGCGCCGAAGCTTACAGCTCT GAGCGCCAGGCTGACCCGAGTCTGAGTCCCATGGGTGAAGCGGAGGCGCCGAAGCTTACAGCTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:205187552..205187703 26863196 MeRIP-seq:(Medium) rs1282285757 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 111007 RMVar_ID_111007 Human_SNP_ID_806213457 m1A Human chr1 + 220136911 220136911 220136911 ATTCATCCTGATGTTGTCGTTAATGGAGGACAAGTAGGTGATTCTCTAAAATGTATTTTATTTTC ATTCATCCTGATGTTGTCGTTAATGGAGGACACGTAGGTGATTCTCTAAAATGTATTTTATTTTC A C IARS2 Ensembl:ENSG00000067704 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:220136862..220136950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_341949,Human_RBP_ID_26799478 Human_Splice_Rec_188997 RMVar_hsa_circ_121447,RMVar_hsa_circ_89771,RMVar_hsa_circ_139673,RMVar_hsa_circ_12197,RMVar_hsa_circ_139674,RMVar_hsa_circ_312606,RMVar_hsa_circ_45758,RMVar_hsa_circ_18074,RMVar_hsa_circ_52944,RMVar_hsa_circ_139679,RMVar_hsa_circ_281003,RMVar_hsa_circ_312339,RMVar_hsa_circ_62281,RMVar_hsa_circ_300087,RMVar_hsa_circ_272153,RMVar_hsa_circ_139681,RMVar_hsa_circ_139680,RMVar_hsa_circ_61738,RMVar_hsa_circ_279723,RMVar_hsa_circ_336267,RMVar_hsa_circ_139678,RMVar_hsa_circ_288878,RMVar_hsa_circ_279357,RMVar_hsa_circ_139683,RMVar_hsa_circ_139684,RMVar_hsa_circ_139685,RMVar_hsa_circ_117805,RMVar_hsa_circ_139687,RMVar_hsa_circ_116603,RMVar_hsa_circ_348858,RMVar_hsa_circ_139686,RMVar_hsa_circ_340830,RMVar_hsa_circ_139688,RMVar_hsa_circ_139689,RMVar_hsa_circ_139691,RMVar_hsa_circ_275856,RMVar_hsa_circ_305920,RMVar_hsa_circ_328570,RMVar_hsa_circ_297305,RMVar_hsa_circ_139692,RMVar_hsa_circ_139690 111008 RMVar_ID_111008 Human_SNP_ID_806224058 m1A Human chr1 - 202880642 202880642 202880642 GCCCAGGGGCTCCCGCTTTTTCTTGCTCTAGAAGAGCAGTATTCAACCTTTTAGCTATGATGACA GCCCAGGGGCTCCCGCTTTTTCTTGCTCTAGATGAGCAGTATTCAACCTTTTAGCTATGATGACA T A RABIF Ensembl:ENSG00000183155 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_338013,Human_RBP_ID_18930337 111009 RMVar_ID_111009 Human_SNP_ID_806226423 m1A Human chr1 + 201209945 201209945 201209945 TATAGGAAGAATTTGGGGGCTCCTGAGGGAATAGGTTCAGGGAGTAAGGCAGGTTTTAGGGATGG TATAGGAAGAATTTGGGGGCTCCTGAGGGAATGGGTTCAGGGAGTAAGGCAGGTTTTAGGGATGG A G IGFN1 Ensembl:ENSG00000163395 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:201209842..201209973 26863196 MeRIP-seq:(Medium) rs374391246 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 111010 RMVar_ID_111010 Human_SNP_ID_806229278 m1A Human chr1 + 206635598 206635598 206635598 AGTGCGCTGAGCTGCAGTGTCTGGTCGAGAGTACCCGTGGGAGCGTCGCGCCGCGGAGGCAGCCG AGTGCGCTGAGCTGCAGTGTCTGGTCGAGAGTGCCCGTGGGAGCGTCGCGCCGCGGAGGCAGCCG A G DYRK3 Ensembl:ENSG00000143479 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr1:206635551..206635784 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_4074723,Human_RBP_ID_9270577,Human_RBP_ID_18416034 111011 RMVar_ID_111011 Human_SNP_ID_806235268 m1A Human chr1 + 173477398 173477398 173477398 TGTCCCAGCGGCGCCCCCTCATCACCGTCGCCATGCCCGGAGGTCTGCTTCTCGGGGACGTGGCT TGTCCCAGCGGCGCCCCCTCATCACCGTCGCCGTGCCCGGAGGTCTGCTTCTCGGGGACGTGGCT A G PRDX6 Ensembl:ENSG00000117592 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr1:173477301..173477584 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_333193,Human_RBP_ID_803319,Human_RBP_ID_4008652,Human_RBP_ID_5456637,Human_RBP_ID_5484873,Human_RBP_ID_10655858,Human_RBP_ID_17456345,Human_RBP_ID_22026090,Human_RBP_ID_22532173,Human_RBP_ID_23345459,Human_RBP_ID_26390096,Human_RBP_ID_26799182,Human_RBP_ID_26847159,Human_RBP_ID_27171773,Human_RBP_ID_27391191 Human_Splice_Rec_158337,Human_Splice_Rec_158339 Human_miRNA_ID_2492198 RMVar_hsa_circ_110680,RMVar_hsa_circ_137631 111012 RMVar_ID_111012 Human_SNP_ID_806246517 m1A Human chr1 - 16624385 16624385 16624385 GGAGGCCCAGTGACAGGTGGAGACGCTGGGGCAAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGG GGAGGCCCAGTGACAGGTGGAGACGCTGGGGCGAGTGGCCCGGGAGAAGGAGGCGCTAGCCAAGG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1629127 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_RBP_ID_224886,Human_RBP_ID_3335036,Human_RBP_ID_5160911,Human_RBP_ID_8171564,Human_RBP_ID_9271990,Human_RBP_ID_9412782,Human_RBP_ID_10648547,Human_RBP_ID_17182579,Human_RBP_ID_17204356,Human_RBP_ID_17224440,Human_RBP_ID_17668418,Human_RBP_ID_18475703,Human_RBP_ID_18926135,Human_RBP_ID_21959340,Human_RBP_ID_21963756,Human_RBP_ID_22849914 Human_Splice_Rec_22724 RMVar_hsa_circ_56321 111013 RMVar_ID_111013 Human_SNP_ID_806248486 m1A Human chr1 + 44636084 44636075 44636084 AGGATGATGCTGTGGACATCGAGCATGAGAACAACAACCGCTTTGAGGAGTATGAGTGGTGTGGA AGGATGATGCTGTGGACATCGAGC_________ACAACCGCTTTGAGGAGTATGAGTGGTGTGGA CATGAGAACA C RNF220 Ensembl:ENSG00000187147 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:44635988..44636158 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 25..33 33 OV 1 - Human_RBP_ID_1432015,Human_RBP_ID_1748707,Human_RBP_ID_9358771,Human_RBP_ID_11002642,Human_RBP_ID_18968239,Human_RBP_ID_21878918,Human_RBP_ID_26314111 Human_Splice_Rec_61520,Human_Splice_Rec_61521,Human_Splice_Rec_61546,Human_Splice_Rec_61547,Human_Splice_Rec_61570,Human_Splice_Rec_61571,Human_Splice_Rec_61598,Human_Splice_Rec_61604,Human_Splice_Rec_61605,Human_Splice_Rec_61618,Human_Splice_Rec_61619,Human_Splice_Rec_61634,Human_Splice_Rec_61635,Human_Splice_Rec_61650,Human_Splice_Rec_61651,Human_Splice_Rec_61660,Human_Splice_Rec_61664,Human_Splice_Rec_61665,Human_Splice_Rec_61672,Human_Splice_Rec_61673,Human_Splice_Rec_61688,Human_Splice_Rec_61689 RMVar_hsa_circ_15965,RMVar_hsa_circ_62880,RMVar_hsa_circ_334205,RMVar_hsa_circ_105978,RMVar_hsa_circ_43671,RMVar_hsa_circ_132405 111014 RMVar_ID_111014 Human_SNP_ID_806256171 m1A Human chr1 - 220058801 220058801 220058801 CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137752 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 111015 RMVar_ID_111015 Human_SNP_ID_806265284 m1A Human chr1 + 25826399 25826399 25826399 CGCCTGGATTGCTGCGGATGAAGAGGAGACATATGCCCGGGTCAGGTAGTTGAGGCAGTAGCTGG CGCCTGGATTGCTGCGGATGAAGAGGAGACATGTGCCCGGGTCAGGTAGTTGAGGCAGTAGCTGG A G MTFR1L Ensembl:ENSG00000117640 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:25826350..25826438 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 10 stomach Human_RBP_ID_3935558,Human_RBP_ID_18965042,Human_RBP_ID_22871207 Human_Splice_Rec_32776,Human_Splice_Rec_32777,Human_Splice_Rec_32788,Human_Splice_Rec_32789,Human_Splice_Rec_32796,Human_Splice_Rec_32797,Human_Splice_Rec_32804,Human_Splice_Rec_32805,Human_Splice_Rec_32814,Human_Splice_Rec_32815,Human_Splice_Rec_32820,Human_Splice_Rec_32821,Human_Splice_Rec_32830,Human_Splice_Rec_32831,Human_Splice_Rec_32850,Human_Splice_Rec_32851,Human_Splice_Rec_32862,Human_Splice_Rec_32863,Human_Splice_Rec_32872,Human_Splice_Rec_32873,Human_Splice_Rec_32884,Human_Splice_Rec_32885,Human_Splice_Rec_32898,Human_Splice_Rec_32904,Human_Splice_Rec_32905,Human_Splice_Rec_32912,Human_Splice_Rec_32913,Human_Splice_Rec_32926,Human_Splice_Rec_32927,Human_Splice_Rec_32936,Human_Splice_Rec_32937,Human_Splice_Rec_32948,Human_Splice_Rec_32949,Human_Splice_Rec_32956,Human_Splice_Rec_32957,Human_Splice_Rec_32966,Human_Splice_Rec_32967,Human_Splice_Rec_32976,Human_Splice_Rec_32977 RMVar_hsa_circ_317241,RMVar_hsa_circ_365084 111016 RMVar_ID_111016 Human_SNP_ID_806275527 m1A Human chr1 + 25808649 25808649 25808649 CAGCCGCCGCCTCACCAAGTGCAGTGTTTGCCACCCGCCACTTCCAGCCCTTCCTTCCCCCGCCA CAGCCGCCGCCTCACCAAGTGCAGTGTTTGCCCCCCGCCACTTCCAGCCCTTCCTTCCCCCGCCA A C SELENON Ensembl:ENSG00000162430 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:25808576..25808736;chr1:25808574..25808726 26863196 MeRIP-seq:(Medium) rs752463295 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_4040304,Human_RBP_ID_23382945 Human_Splice_Rec_32670,Human_Splice_Rec_32696,Human_Splice_Rec_32718 RMVar_hsa_circ_6205,RMVar_hsa_circ_35596,RMVar_hsa_circ_105872,RMVar_hsa_circ_114934,RMVar_hsa_circ_364975,RMVar_hsa_circ_130585,RMVar_hsa_circ_322366,RMVar_hsa_circ_17014,RMVar_hsa_circ_18474,RMVar_hsa_circ_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586,RMVar_hsa_circ_44592,RMVar_hsa_circ_130590,RMVar_hsa_circ_102700,RMVar_hsa_circ_331113,RMVar_hsa_circ_85638,RMVar_hsa_circ_130591,RMVar_hsa_circ_130589 111017 RMVar_ID_111017 Human_SNP_ID_806281630 m1A Human chr1 - 161749944 161749944 161749944 CTGTTAGCACGGCCGTGATGCCCGCTTCCCTCAGGTGATCTGGCTCCGCGACGGCCGCGGCCCCA CTGTTAGCACGGCCGTGATGCCCGCTTCCCTCGGGTGATCTGGCTCCGCGACGGCCGCGGCCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr1:161749801..161750075;chr1:161749801..161750019 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111018 RMVar_ID_111018 Human_SNP_ID_806305800 m1A Human chr1 - 155268816 155268816 155268816 CCGGCCCCCGCTCCGACACCTGGCTTGCTCCGACCCCCCCTGCCCCCCGACAGCAGCACAGCAGC CCGGCCCCCGCTCCGACACCTGGCTTGCTCCGGCCCCCCCTGCCCCCCGACAGCAGCACAGCAGC T C CLK2 Ensembl:ENSG00000176444 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:155268680..155268975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_23094,Human_RBP_ID_10595149 RMVar_hsa_circ_136546,RMVar_hsa_circ_108543,RMVar_hsa_circ_291123,RMVar_hsa_circ_113999,RMVar_hsa_circ_101046,RMVar_hsa_circ_136550,RMVar_hsa_circ_136551,RMVar_hsa_circ_88657,RMVar_hsa_circ_136553,RMVar_hsa_circ_98497,RMVar_hsa_circ_136554,RMVar_hsa_circ_136555 111019 RMVar_ID_111019 Human_SNP_ID_806308037 m1A Human chr1 + 231338394 231338394 231338394 CCCGCCTGTGATCCTGGCAACGATGGATGATGACTTGATGTTGGCACTGCGGCTTCAGGAGGAGT CCCGCCTGTGATCCTGGCAACGATGGATGATGCCTTGATGTTGGCACTGCGGCTTCAGGAGGAGT A C SPRTN Ensembl:ENSG00000010072 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr1:231338344..231338593 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mantle_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_RBP_ID_345784,Human_RBP_ID_1423826,Human_RBP_ID_1739942,Human_RBP_ID_4032398,Human_RBP_ID_5777582,Human_RBP_ID_10836559,Human_RBP_ID_23372675 111020 RMVar_ID_111020 Human_SNP_ID_806308518 m1A Human chr1 + 156676658 156676658 156676658 CCGGCCCAGCCGCTCGCGGGCCTGGCCCAGCGACGTCTCCATGTGTGCCACGCGCTCCTGGTAGC CCGGCCCAGCCGCTCGCGGGCCTGGCCCAGCGTCGTCTCCATGTGTGCCACGCGCTCCTGGTAGC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr1:156676476..156676694 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111021 RMVar_ID_111021 Human_SNP_ID_806317093 m1A Human chr1 + 110246815 110246815 110246815 ACACATTTATTGGGTACAAGTGCAATTTTGCCACATGCCTAGTTGCACAGTAGTTATATCAGGGC ACACATTTATTGGGTACAAGTGCAATTTTGCCTCATGCCTAGTTGCACAGTAGTTATATCAGGGC A T KCNC4 Ensembl:ENSG00000116396 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr1:110246777..110246887 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111022 RMVar_ID_111022 Human_SNP_ID_850742678 m1A Human chr4 - 182144760 182144760 182144760 AAGGAAGGAGGGCGCGCCGGCGGCGGCGCCGCACTTACCGCGCTCGGCTCGCCCGCGCCGCCGGC AAGGAAGGAGGGCGCGCCGGCGGCGGCGCCGCCCTTACCGCGCTCGGCTCGCCCGCGCCGCCGGC T G TENM3-AS1 Ensembl:ENSG00000177822 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:182144755..182144917 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111023 RMVar_ID_111023 Human_SNP_ID_850768604 m1A Human chr4 - 152780036 152780036 152780036 CAACTGCAGCTGTCACAAATTCACACTGACCAACCGCCGAGGACAGTCGGACCGGCGACCTCTCA CAACTGCAGCTGTCACAAATTCACACTGACCAGCCGCCGAGGACAGTCGGACCGGCGACCTCTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:152779986..152807212 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 111024 RMVar_ID_111024 Human_SNP_ID_850817334 m1A Human chr4 - 25234069 25234069 25234069 CTCTGCATGGCGCGGAACGGGAGCGACCGGGTAGAACGGACGCCACCTCACCAGCGCACGGGCAC CTCTGCATGGCGCGGAACGGGAGCGACCGGGTTGAACGGACGCCACCTCACCAGCGCACGGGCAC T A - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 111025 RMVar_ID_111025 Human_SNP_ID_850817845 m1A Human chr4 - 1249514 1249514 1249514 CGGGAGGGCGGCAGCTGGCGGAGCGGGAAGGGAGCGGGGCGGCTGCGGCTGCGGCGCGGAGGAGC CGGGAGGGCGGCAGCTGGCGGAGCGGGAAGGGTGCGGGGCGGCTGCGGCTGCGGCGCGGAGGAGC T A CTBP1 Ensembl:ENSG00000159692 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:1249278..1249949;chr4:1249270..1249744;chr4:1249218..1249723;chr4:1249299..1249693 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 111026 RMVar_ID_111026 Human_SNP_ID_850919630 m1A Human chr4 - 82355381 82355381 82355381 GTTTTATTTTAGACCAGCAGAGTGGTTATGGGAAGGTATCCAGGCGAGGTGGTCATCAAAATAGC GTTTTATTTTAGACCAGCAGAGTGGTTATGGGTAGGTATCCAGGCGAGGTGGTCATCAAAATAGC T A HNRNPD Ensembl:ENSG00000138668 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:82355239..82355440 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 3 head and neck Human_RBP_ID_71398,Human_RBP_ID_249002,Human_RBP_ID_625352,Human_RBP_ID_785970,Human_RBP_ID_1389086,Human_RBP_ID_1981400,Human_RBP_ID_3744386,Human_RBP_ID_7331649,Human_RBP_ID_8236525,Human_RBP_ID_9163353,Human_RBP_ID_15208158,Human_RBP_ID_18032402,Human_RBP_ID_22458340,Human_RBP_ID_24547881,Human_RBP_ID_26350129,Human_RBP_ID_27824237 Human_Splice_Rec_573820,Human_Splice_Rec_573821,Human_Splice_Rec_573836,Human_Splice_Rec_573837,Human_Splice_Rec_573846,Human_Splice_Rec_573847,Human_Splice_Rec_573862,Human_Splice_Rec_573863,Human_Splice_Rec_573868,Human_Splice_Rec_573878 RMVar_hsa_circ_3832,RMVar_hsa_circ_226956,RMVar_hsa_circ_320661,RMVar_hsa_circ_226957,RMVar_hsa_circ_344031,RMVar_hsa_circ_30856,RMVar_hsa_circ_226958 111027 RMVar_ID_111027 Human_SNP_ID_850986783 m1A Human chr4 - 98901950 98901950 98901950 GAAACCACCCCTACTCCTAATCCCCCGACTACAGAAGAGGAGAAAACGGAATCTAATCAGGAGGT GAAACCACCCCTACTCCTAATCCCCCGACTACGGAAGAGGAGAAAACGGAATCTAATCAGGAGGT T C EIF4E Ensembl:ENSG00000151247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:98901901..98902000;chr4:98901839..98901978;chr4:98901847..98902023;chr4:98901880..98902027 26863196 MeRIP-seq:(Medium) rs538537081 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,STAD,stomach adenocarcinoma,colon adenocarcinoma,large_intestine adenocarcinoma 11 stomach,large intestine Human_RBP_ID_1641541,Human_RBP_ID_4794375,Human_RBP_ID_5210569,Human_RBP_ID_7342193,Human_RBP_ID_17409308,Human_RBP_ID_26349471 Human_Splice_Rec_584906,Human_Splice_Rec_584907,Human_Splice_Rec_584918,Human_Splice_Rec_584919,Human_Splice_Rec_584930,Human_Splice_Rec_584931,Human_Splice_Rec_584938,Human_Splice_Rec_584939,Human_Splice_Rec_584950,Human_Splice_Rec_584951,Human_Splice_Rec_584962,Human_Splice_Rec_584963,Human_Splice_Rec_584982,Human_Splice_Rec_584983,Human_Splice_Rec_584994,Human_Splice_Rec_584995 RMVar_hsa_circ_35056,RMVar_hsa_circ_39129,RMVar_hsa_circ_29622,RMVar_hsa_circ_41106 111028 RMVar_ID_111028 Human_SNP_ID_851004086 m1A Human chr4 - 3767777 3767777 3767777 GCTGAAGAAGAAGGGGAACCAGCAGAGCACGAACACGCCCATGACCACAGCCAGCACAAAGGTGA GCTGAAGAAGAAGGGGAACCAGCAGAGCACGAGCACGCCCATGACCACAGCCAGCACAAAGGTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:3767585..3768075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 111029 RMVar_ID_111029 Human_SNP_ID_851023826 m1A Human chr4 - 82426621 82426621 82426621 ATCATTGTGCATTGTTTCAGGTCAGGGCCAAAACTGGAACCAAGGATTTAATAACTATTATGATC ATCATTGTGCATTGTTTCAGGTCAGGGCCAAAGCTGGAACCAAGGATTTAATAACTATTATGATC T C HNRNPDL Ensembl:ENSG00000152795 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:82426451..82426650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_RBP_ID_837788,Human_RBP_ID_1037459,Human_RBP_ID_1069314,Human_RBP_ID_1981532,Human_RBP_ID_7332152,Human_RBP_ID_9396492,Human_RBP_ID_15209392,Human_RBP_ID_18413549,Human_RBP_ID_18826959,Human_RBP_ID_19014492,Human_RBP_ID_26349427,Human_RBP_ID_27824251 Human_Splice_Rec_573930,Human_Splice_Rec_573944,Human_Splice_Rec_573970,Human_Splice_Rec_573982,Human_Splice_Rec_573996,Human_Splice_Rec_574012,Human_Splice_Rec_574030,Human_Splice_Rec_574048,Human_Splice_Rec_574058 Human_miRNA_ID_2489844,Human_miRNA_ID_2751929 RMVar_hsa_circ_286669,RMVar_hsa_circ_366678,RMVar_hsa_circ_5743,RMVar_hsa_circ_95870,RMVar_hsa_circ_226963,RMVar_hsa_circ_60593 111030 RMVar_ID_111030 Human_SNP_ID_851082120 m1A Human chr4 + 82359567 82359567 82359567 GGATCTAACTTCAGAGTGCAGTCTACAACTTCACCAAATTTGGAAAAGTAGTCCTTCAGATCTTT GGATCTAACTTCAGAGTGCAGTCTACAACTTCCCCAAATTTGGAAAAGTAGTCCTTCAGATCTTT A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:82359551..82359575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 111031 RMVar_ID_111031 Human_SNP_ID_851104367 m1A Human chr4 - 24549024 24549024 24549024 AGTATTCGTTTTTAGACTCACTTTTATTTTGTAGGAAATTGATGAAGCCTGTAAGAGAATAAAGC AGTATTCGTTTTTAGACTCACTTTTATTTTGTTGGAAATTGATGAAGCCTGTAAGAGAATAAAGC T A DHX15 Ensembl:ENSG00000109606 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:24548988..24554790 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_72543,Human_RBP_ID_1977385,Human_RBP_ID_22679076 RMVar_hsa_circ_7805,RMVar_hsa_circ_65157,RMVar_hsa_circ_73969,RMVar_hsa_circ_361475,RMVar_hsa_circ_28349,RMVar_hsa_circ_332433,RMVar_hsa_circ_342014,RMVar_hsa_circ_319933 111032 RMVar_ID_111032 Human_SNP_ID_851104369 m1A Human chr4 - 24549024 24549024 24549024 AGTATTCGTTTTTAGACTCACTTTTATTTTGTAGGAAATTGATGAAGCCTGTAAGAGAATAAAGC AGTATTCGTTTTTAGACTCACTTTTATTTTGTGGGAAATTGATGAAGCCTGTAAGAGAATAAAGC T C DHX15 Ensembl:ENSG00000109606 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:24548988..24554790 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_72543,Human_RBP_ID_1977385,Human_RBP_ID_22679076 RMVar_hsa_circ_7805,RMVar_hsa_circ_65157,RMVar_hsa_circ_73969,RMVar_hsa_circ_361475,RMVar_hsa_circ_28349,RMVar_hsa_circ_332433,RMVar_hsa_circ_342014,RMVar_hsa_circ_319933 111033 RMVar_ID_111033 Human_SNP_ID_851155028 m1A Human chr4 - 151665595 151665595 151665595 GCAGGATTTGCTCTTCTCCCGTGGATAGACTCAGTTCTCTGCTGTTTTTCTTTGGCATGTCCACG GCAGGATTTGCTCTTCTCCCGTGGATAGACTCCGTTCTCTGCTGTTTTTCTTTGGCATGTCCACG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:151665546..151665724 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111034 RMVar_ID_111034 Human_SNP_ID_851172234 m1A Human chr4 - 127965092 127965092 127965092 CTGCGGAACGAAAGTGAACAGGAGCCGCTCTTAGGCGACACACCTGGAAGCAGGTGAGCGGATCC CTGCGGAACGAAAGTGAACAGGAGCCGCTCTTGGGCGACACACCTGGAAGCAGGTGAGCGGATCC T C MFSD8 Ensembl:ENSG00000164073 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:127965063..127965154 26863196 MeRIP-seq:(Medium) rs1160479250 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 19 large intestine Human_RBP_ID_9397435,Human_RBP_ID_18424636,Human_RBP_ID_19014583 Human_Splice_Rec_605291,Human_Splice_Rec_605317,Human_Splice_Rec_605339,Human_Splice_Rec_605359,Human_Splice_Rec_605377,Human_Splice_Rec_605397,Human_Splice_Rec_605421,Human_Splice_Rec_605473,Human_Splice_Rec_605489,Human_Splice_Rec_605503,Human_Splice_Rec_605523,Human_Splice_Rec_605555,Human_Splice_Rec_605573,Human_Splice_Rec_605633,Human_Splice_Rec_605657,Human_Splice_Rec_605675,Human_Splice_Rec_605725,Human_Splice_Rec_605745,Human_Splice_Rec_605765,Human_Splice_Rec_605783,Human_Splice_Rec_605793,Human_Splice_Rec_605807,Human_Splice_Rec_605839,Human_Splice_Rec_605857,Human_Splice_Rec_605875,Human_Splice_Rec_605915,Human_Splice_Rec_605945,Human_Splice_Rec_605963,Human_Splice_Rec_605983,Human_Splice_Rec_606031,Human_Splice_Rec_606043,Human_Splice_Rec_606081,Human_Splice_Rec_606095,Human_Splice_Rec_606107,Human_Splice_Rec_606121,Human_Splice_Rec_606133,Human_Splice_Rec_606151,Human_Splice_Rec_606161,Human_Splice_Rec_606169,Human_Splice_Rec_606177 RMVar_hsa_circ_95675,RMVar_hsa_circ_264921,RMVar_hsa_circ_228535,RMVar_hsa_circ_79581,RMVar_hsa_circ_228536 111035 RMVar_ID_111035 Human_SNP_ID_851218819 m1A Human chr4 - 56467698 56467698 56467698 TTGAGAGCGCGCGTGAAGTCGCCGTTCTGGCCATACCGGTTCACTTCACTCCACAGCGCAGGTAC TTGAGAGCGCGCGTGAAGTCGCCGTTCTGGCCGTACCGGTTCACTTCACTCCACAGCGCAGGTAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:56467651..56467782 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111036 RMVar_ID_111036 Human_SNP_ID_851241267 m1A Human chr4 + 1354801 1354801 1354801 TGCTCTCATCCACGCCGCCCGCGACACACTCAAGCTCATCCGGAACAAGTTCCTGCCGGCTGTGT TGCTCTCATCCACGCCGCCCGCGACACACTCAGGCTCATCCGGAACAAGTTCCTGCCGGCTGTGT A G UVSSA Ensembl:ENSG00000163945 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1353103..1355104 32194978 MeRIP-seq:(Medium) rs1325045818 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_RBP_ID_9396895 Human_Splice_Rec_537434,Human_Splice_Rec_537435,Human_Splice_Rec_537456,Human_Splice_Rec_537457,Human_Splice_Rec_537480,Human_Splice_Rec_537481,Human_Splice_Rec_537497 RMVar_hsa_circ_24148,RMVar_hsa_circ_92661,RMVar_hsa_circ_324613,RMVar_hsa_circ_119583,RMVar_hsa_circ_353663,RMVar_hsa_circ_224243,RMVar_hsa_circ_335689,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244,RMVar_hsa_circ_31335 111037 RMVar_ID_111037 Human_SNP_ID_851252444 m1A Human chr4 - 173332789 173332789 173332789 GGTACAGTGTCATCTTTTTTAAAGCCGTGGATAAGACTAGGTATAGGTAATAACTGTAGAAAACC GGTACAGTGTCATCTTTTTTAAAGCCGTGGATGAGACTAGGTATAGGTAATAACTGTAGAAAACC T C HMGB2 Ensembl:ENSG00000164104 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:173332787..173332926 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_2832972,Human_RBP_ID_19123186,Human_RBP_ID_27842012 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578 111038 RMVar_ID_111038 Human_SNP_ID_851293062 m1A Human chr4 + 162712294 162712294 162712294 TGCCTATCCACCCTGTGGTGCCCAACCCGTACACTCTTTCATCCTCAATACCTTCCTCCACAACT TGCCTATCCACCCTGTGGTGCCCAACCCGTACTCTCTTTCATCCTCAATACCTTCCTCCACAACT A T AC021134.1 Ensembl:ENSG00000248431 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:162712261..162712349 26863196 MeRIP-seq:(Medium) rs544603862 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111039 RMVar_ID_111039 Human_SNP_ID_851295340 m1A Human chr4 + 83035244 83035244 83035244 AGCTGGGAGAAAGATGGCGGCAGCCGTGCGACAGGATTTGGCCCAGCTCATGAATTCGAGCGGCT AGCTGGGAGAAAGATGGCGGCAGCCGTGCGACCGGATTTGGCCCAGCTCATGAATTCGAGCGGCT A C COPS4 Ensembl:ENSG00000138663 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:83035105..83035334 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 12 large intestine Human_RBP_ID_4792328,Human_RBP_ID_9163581 Human_Splice_Rec_575379,Human_Splice_Rec_575395,Human_Splice_Rec_575399,Human_Splice_Rec_575411,Human_Splice_Rec_575415,Human_Splice_Rec_575433,Human_Splice_Rec_575441,Human_Splice_Rec_575447,Human_Splice_Rec_575467 111040 RMVar_ID_111040 Human_SNP_ID_851336217 m1A Human chr4 - 39698288 39698288 39698288 CCCGCAGCTGATTCGTACCCGCCTCCTCCGCCACCGCTACGACCACCGCCACCGCCGCCACCTCT CCCGCAGCTGATTCGTACCCGCCTCCTCCGCCGCCGCTACGACCACCGCCACCGCCGCCACCTCT T C lnc-SMIM14-7 RNACentral:URS00008B6C4F lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:39698176..39737423 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 STAD 1 - 111041 RMVar_ID_111041 Human_SNP_ID_851383590 m1A Human chr4 + 108622195 108622195 108622195 CCAAAATCTGCATGTGGTGTGTGCCCAGGCAGACTTCGAGGGGTAAGTGTACCTTTTACTGTGTG CCAAAATCTGCATGTGGTGTGTGCCCAGGCAGGCTTCGAGGGGTAAGTGTACCTTTTACTGTGTG A G RPL34 Ensembl:ENSG00000109475 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:108621951..108622230 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung bronchioloalveolar_adenocarcinoma 5 lung Human_RBP_ID_249332,Human_RBP_ID_611186,Human_RBP_ID_786982,Human_RBP_ID_838193,Human_RBP_ID_1971655,Human_RBP_ID_9334765,Human_RBP_ID_17662121,Human_RBP_ID_18195033,Human_RBP_ID_22458412,Human_RBP_ID_23214042,Human_RBP_ID_24030040,Human_RBP_ID_26825576 Human_Splice_Rec_591180,Human_Splice_Rec_591181,Human_Splice_Rec_591188,Human_Splice_Rec_591189,Human_Splice_Rec_591198,Human_Splice_Rec_591199,Human_Splice_Rec_591204,Human_Splice_Rec_591210,Human_Splice_Rec_591211,Human_Splice_Rec_591218,Human_Splice_Rec_591219 Human_miRNA_ID_2455070 RMVar_hsa_circ_23435,RMVar_hsa_circ_372800,RMVar_hsa_circ_227920,RMVar_hsa_circ_356074 111042 RMVar_ID_111042 Human_SNP_ID_851461070 m1A Human chr4 - 141636713 141636713 141636713 CATCGAGTCCTGGCTGCAGGGTGGGGGGCGACAGCCACCGCAGCCGGGAGGGTGCGGCCACCCAG CATCGAGTCCTGGCTGCAGGGTGGGGGGCGACCGCCACCGCAGCCGGGAGGGTGCGGCCACCCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:141636604..141636748 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - 111043 RMVar_ID_111043 Human_SNP_ID_851464422 m1A Human chr4 - 49118563 49118563 49118563 AGTGGAATGGAATGGAATGGAATGGAATGGAAAGGAATCAACTCGAAGGGAATGGAATGGAATGG AGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATCAACTCGAAGGGAATGGAATGGAATGG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49118561..49118752 26863196 MeRIP-seq:(Medium) rs201173269 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111044 RMVar_ID_111044 Human_SNP_ID_851466787 m1A Human chr4 + 118752703 118752703 118752703 TAAATTATAAAACACTTGATATTTACTTATGAATCACAGATTGGGATTCTTGATAGTTGACAAGG TAAATTATAAAACACTTGATATTTACTTATGACTCACAGATTGGGATTCTTGATAGTTGACAAGG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:118741030..118752706 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111045 RMVar_ID_111045 Human_SNP_ID_851475759 m1A Human chr4 + 182346591 182346589 182346591 TTCTGAAAGACATTCTTAAAAAAAAAAAAAAGAAAAGAAACTAACACTGAACATATACTCACTAG TTCTGAAAGACATTCTTAAAAAAAAAAAAAA__AAAGAAACTAACACTGAACATATACTCACTAG AGA A TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182346590..182346721 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 LMS 1 - RMVar_hsa_circ_96182,RMVar_hsa_circ_282218,RMVar_hsa_circ_119113,RMVar_hsa_circ_229672,RMVar_hsa_circ_14204,RMVar_hsa_circ_47790,RMVar_hsa_circ_229673,RMVar_hsa_circ_229674 111046 RMVar_ID_111046 Human_SNP_ID_851514603 m1A Human chr4 - 25802425 25802425 25802425 GTTGTATAGTTTGGTTGGAGGCCAGGGGAGTGAGAGGCTGTCTTCAATGAATCTTGGGTATAAAC GTTGTATAGTTTGGTTGGAGGCCAGGGGAGTGGGAGGCTGTCTTCAATGAATCTTGGGTATAAAC T C SEL1L3 Ensembl:ENSG00000091490 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:25802390..25804619 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_3966669,Human_RBP_ID_18447499,Human_RBP_ID_18822983 Human_Splice_Rec_551550,Human_Splice_Rec_551596,Human_Splice_Rec_551652 RMVar_hsa_circ_1064,RMVar_hsa_circ_91944,RMVar_hsa_circ_225171,RMVar_hsa_circ_291101,RMVar_hsa_circ_353211,RMVar_hsa_circ_300667,RMVar_hsa_circ_29009,RMVar_hsa_circ_55676,RMVar_hsa_circ_61893,RMVar_hsa_circ_225172,RMVar_hsa_circ_225174,RMVar_hsa_circ_225173,RMVar_hsa_circ_305199,RMVar_hsa_circ_9054,RMVar_hsa_circ_83893,RMVar_hsa_circ_225182,RMVar_hsa_circ_326008,RMVar_hsa_circ_352818,RMVar_hsa_circ_290930,RMVar_hsa_circ_225184,RMVar_hsa_circ_225185,RMVar_hsa_circ_298383,RMVar_hsa_circ_355128,RMVar_hsa_circ_225183,RMVar_hsa_circ_323607,RMVar_hsa_circ_320667,RMVar_hsa_circ_11178,RMVar_hsa_circ_56388,RMVar_hsa_circ_225194,RMVar_hsa_circ_225192,RMVar_hsa_circ_225193,RMVar_hsa_circ_225191,RMVar_hsa_circ_354916,RMVar_hsa_circ_345882,RMVar_hsa_circ_285300,RMVar_hsa_circ_350405,RMVar_hsa_circ_274460,RMVar_hsa_circ_40829,RMVar_hsa_circ_225196,RMVar_hsa_circ_68134,RMVar_hsa_circ_269540,RMVar_hsa_circ_268329,RMVar_hsa_circ_225204,RMVar_hsa_circ_317434,RMVar_hsa_circ_23016,RMVar_hsa_circ_110703,RMVar_hsa_circ_225197,RMVar_hsa_circ_353273,RMVar_hsa_circ_23279,RMVar_hsa_circ_347855,RMVar_hsa_circ_225198,RMVar_hsa_circ_369149,RMVar_hsa_circ_318305,RMVar_hsa_circ_285048,RMVar_hsa_circ_295516,RMVar_hsa_circ_284105,RMVar_hsa_circ_225200,RMVar_hsa_circ_225202,RMVar_hsa_circ_225203,RMVar_hsa_circ_225201,RMVar_hsa_circ_225199 111047 RMVar_ID_111047 Human_SNP_ID_851537018 m1A Human chr4 + 1804434 1804434 1804434 TCTTCCTGTTCATCCTGGTGGTGGCGGCTGTGACGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAA TCTTCCTGTTCATCCTGGTGGTGGCGGCTGTGGCGCTCTGCCGCCTGCGCAGCCCCCCCAAGAAA A G FGFR3 Ensembl:ENSG00000068078 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1803806..1804599 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_9396923,Human_RBP_ID_26771321 Human_Splice_Rec_537979,Human_Splice_Rec_538013,Human_Splice_Rec_538045,Human_Splice_Rec_538111,Human_Splice_Rec_538173 RMVar_hsa_circ_82815,RMVar_hsa_circ_119196,RMVar_hsa_circ_224274,RMVar_hsa_circ_224275 111048 RMVar_ID_111048 Human_SNP_ID_851562487 m1A Human chr4 + 1289981 1289981 1289981 GACCCTGAAGGTCCAGGAGTACCCGACCCTCAAGGTGGGCGCCTGCGCCGCGCAGGCTGAGGGCA GACCCTGAAGGTCCAGGAGTACCCGACCCTCAGGGTGGGCGCCTGCGCCGCGCAGGCTGAGGGCA A G MAEA Ensembl:ENSG00000090316 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1289932..1290023 26863196 MeRIP-seq:(Medium) rs773549747 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas Human_RBP_ID_4794808,Human_RBP_ID_19014105,Human_RBP_ID_19122000,Human_RBP_ID_23034775,Human_RBP_ID_26349009 Human_Splice_Rec_537245,Human_Splice_Rec_537263,Human_Splice_Rec_537267,Human_Splice_Rec_537277,Human_Splice_Rec_537287,Human_Splice_Rec_537301,Human_Splice_Rec_537317,Human_Splice_Rec_537323,Human_Splice_Rec_537331,Human_Splice_Rec_537343,Human_Splice_Rec_537345,Human_Splice_Rec_537353 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238 111049 RMVar_ID_111049 Human_SNP_ID_851562730 m1A Human chr4 + 83012752 83012745 83012753 CTCGCAGCGGGGGCCGGTTCCCCCTTCCCGCCAGCCCGCCCAGGAGCCCCCATCCCGGGGGCTGA CTCGCAGCGGGGGCCGGTTCCCCCTT________CCCGCCCAGGAGCCCCCATCCCGGGGGCTGA TCCCGCCAG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:83012751..83012909 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 27..34 33 PRAD 1 - 111050 RMVar_ID_111050 Human_SNP_ID_851563421 m1A Human chr4 - 2747837 2747837 2747837 AGCGAGAGAAGGAAGTCGTCCTGCTACGGAGGAGCATGGCAGAAGGGGAGCGCGCCCGGGCCGCC AGCGAGAGAAGGAAGTCGTCCTGCTACGGAGGCGCATGGCAGAAGGGGAGCGCGCCCGGGCCGCC T G TNIP2 Ensembl:ENSG00000168884 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2747787..2756090 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THYM 1 - RMVar_hsa_circ_347174,RMVar_hsa_circ_224391,RMVar_hsa_circ_85395 111051 RMVar_ID_111051 Human_SNP_ID_851609907 m1A Human chr4 - 1026366 1026366 1026366 GCAGGGAAAGTCCCTCATCAACTATGAGCCTCACGGCACACGTACTGCAGGCTTCACGGCACACC GCAGGGAAAGTCCCTCATCAACTATGAGCCTCGCGGCACACGTACTGCAGGCTTCACGGCACACC T C lnc-RNF212-3,lnc-RNF212-3:2,lnc-RNF212-3:3 RNACentral:URS00008C2DE4,RNACentral:URS00008C1F26,RNACentral:URS00009B8989 lincRNA,lincRNA,lincRNA intron,exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1026247..1026597 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111052 RMVar_ID_111052 Human_SNP_ID_851619309 m1A Human chr4 - 122922561 122922561 122922561 GACGAATTAAGCGGCGTGGAGATGCGGCAGCCACTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC GACGAATTAAGCGGCGTGGAGATGCGGCAGCCGCTGAGCTGGGGCCGCTGGCGCGCGATGCTTGC T C NUDT6 Ensembl:ENSG00000170917 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:122922362..122922577 26863196 MeRIP-seq:(Medium) rs13134412 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,colon adenocarcinoma,COCA,rectum adenocarcinoma,large_intestine adenocarcinoma,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 15 caecum,bladder,urinary tract,head and neck,large intestine GWAS_ID_9074,GWAS_ID_9075,GWAS_ID_9076 111053 RMVar_ID_111053 Human_SNP_ID_851623533 m1A Human chr4 + 183851045 183851045 183851045 AGGATGAGAGAAACGATGAGGGAAAGGATGAGAGAAACGATGAGAGAAAGGATGAGGGAAAGGAT AGGATGAGAGAAACGATGAGGGAAAGGATGAGGGAAACGATGAGAGAAAGGATGAGGGAAAGGAT A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:183850891..183851301 26863196 MeRIP-seq:(Medium) rs376506542 Functional Loss SNV ICGC 33..33 33 MELA 1 - 111054 RMVar_ID_111054 Human_SNP_ID_851697075 m1A Human chr4 - 99949742 99949742 99949742 TCCTCCTCCGCTCGCGGGCGTGTGCGCGCCGCAGGCTGGCGGTAAGGCTGGAAAGGACTCCGGAA TCCTCCTCCGCTCGCGGGCGTGTGCGCGCCGCTGGCTGGCGGTAAGGCTGGAAAGGACTCCGGAA T A H2AZ1 Ensembl:ENSG00000164032 Protein coding intron GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr4:99949701..99949750;chr4:99949626..99949849;chr4:99949718..99949798;chr4:99949651..99949750 26863196,26863410,26863196,32194978 MeRIP-seq:(Medium) rs113550334 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_940952,Human_RBP_ID_4796078,Human_RBP_ID_5150652,Human_RBP_ID_18195028,Human_RBP_ID_19121758,Human_RBP_ID_22458672,Human_RBP_ID_22679329,Human_RBP_ID_25829847,Human_RBP_ID_27159983,Human_RBP_ID_27721981 Human_Splice_Rec_586243,Human_Splice_Rec_586251,Human_Splice_Rec_586259,Human_Splice_Rec_586267,Human_Splice_Rec_586275 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 111055 RMVar_ID_111055 Human_SNP_ID_851705668 m1A Human chr4 + 82429388 82429388 82429388 GGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCAGCGGCGGCGGAGCGTTGTATGGAGCTGGATTT GGGTGCTGGCGCGCAGTCCGGGTCGCGGCAGCGGCGGCGGCGGAGCGTTGTATGGAGCTGGATTT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:82429293..82429450 26863196 MeRIP-seq:(Medium) rs750185803 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 8 stomach 111056 RMVar_ID_111056 Human_SNP_ID_851734267 m1A Human chr4 - 25312889 25312889 25312889 GGGCGGGGACGGCAGGATCCAAAGGAAGCACCACCTCCATTCCCGAGCTTCCCCGGCACCCTGCG GGGCGGGGACGGCAGGATCCAAAGGAAGCACCGCCTCCATTCCCGAGCTTCCCCGGCACCCTGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:25312812..25312935 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 111057 RMVar_ID_111057 Human_SNP_ID_851771735 m1A Human chr4 - 73177498 73177498 73177498 GAGTCTTTCATTTTGGATCAGGATGATTTGGAAAATCCAATGCTGGAAACAGCTTCCAAGTTGCT GAGTCTTTCATTTTGGATCAGGATGATTTGGATAATCCAATGCTGGAAACAGCTTCCAAGTTGCT T A ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:73177447..73222987 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_71340,Human_RBP_ID_1980659,Human_RBP_ID_3966826,Human_RBP_ID_5150837,Human_RBP_ID_5531627,Human_RBP_ID_9396391,Human_RBP_ID_15194239,Human_RBP_ID_19013769,Human_RBP_ID_21082243,Human_RBP_ID_22826421,Human_RBP_ID_23034811,Human_RBP_ID_24063406,Human_RBP_ID_24561804,Human_RBP_ID_25829218,Human_RBP_ID_26349359,Human_RBP_ID_27824196 Human_Splice_Rec_568430,Human_Splice_Rec_568646 Human_miRNA_ID_972694,Human_miRNA_ID_2440720 RMVar_hsa_circ_8226,RMVar_hsa_circ_91835,RMVar_hsa_circ_11946,RMVar_hsa_circ_226542,RMVar_hsa_circ_341602,RMVar_hsa_circ_363535,RMVar_hsa_circ_45419,RMVar_hsa_circ_314730,RMVar_hsa_circ_47569,RMVar_hsa_circ_226563,RMVar_hsa_circ_115715,RMVar_hsa_circ_334470,RMVar_hsa_circ_226565,RMVar_hsa_circ_226566,RMVar_hsa_circ_3611,RMVar_hsa_circ_4811,RMVar_hsa_circ_301400,RMVar_hsa_circ_226575,RMVar_hsa_circ_226573,RMVar_hsa_circ_280586,RMVar_hsa_circ_226574 111058 RMVar_ID_111058 Human_SNP_ID_851771738 m1A Human chr4 - 73177498 73177498 73177498 GAGTCTTTCATTTTGGATCAGGATGATTTGGAAAATCCAATGCTGGAAACAGCTTCCAAGTTGCT GAGTCTTTCATTTTGGATCAGGATGATTTGGACAATCCAATGCTGGAAACAGCTTCCAAGTTGCT T G ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:73177447..73222987 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_71340,Human_RBP_ID_1980659,Human_RBP_ID_3966826,Human_RBP_ID_5150837,Human_RBP_ID_5531627,Human_RBP_ID_9396391,Human_RBP_ID_15194239,Human_RBP_ID_19013769,Human_RBP_ID_21082243,Human_RBP_ID_22826421,Human_RBP_ID_23034811,Human_RBP_ID_24063406,Human_RBP_ID_24561804,Human_RBP_ID_25829218,Human_RBP_ID_26349359,Human_RBP_ID_27824196 Human_Splice_Rec_568430,Human_Splice_Rec_568646 Human_miRNA_ID_972694,Human_miRNA_ID_2440720 RMVar_hsa_circ_8226,RMVar_hsa_circ_91835,RMVar_hsa_circ_11946,RMVar_hsa_circ_226542,RMVar_hsa_circ_341602,RMVar_hsa_circ_363535,RMVar_hsa_circ_45419,RMVar_hsa_circ_314730,RMVar_hsa_circ_47569,RMVar_hsa_circ_226563,RMVar_hsa_circ_115715,RMVar_hsa_circ_334470,RMVar_hsa_circ_226565,RMVar_hsa_circ_226566,RMVar_hsa_circ_3611,RMVar_hsa_circ_4811,RMVar_hsa_circ_301400,RMVar_hsa_circ_226575,RMVar_hsa_circ_226573,RMVar_hsa_circ_280586,RMVar_hsa_circ_226574 111059 RMVar_ID_111059 Human_SNP_ID_851792951 m1A Human chr4 + 1978701 1978701 1978701 CGTGTGTGGCAAACCTTCGACTTCATTTTGCCACCTCTGCCCCAATTCGTTCTGTAAGGAGCACC CGTGTGTGGCAAACCTTCGACTTCATTTTGCCCCCTCTGCCCCAATTCGTTCTGTAAGGAGCACC A C NSD2 Ensembl:ENSG00000109685 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1978626..1978700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_618401,Human_RBP_ID_941593,Human_RBP_ID_1975922,Human_RBP_ID_3735488,Human_RBP_ID_5150923,Human_RBP_ID_5326272,Human_RBP_ID_9334570,Human_RBP_ID_18023777,Human_RBP_ID_18447444,Human_RBP_ID_18822085,Human_RBP_ID_22095381,Human_RBP_ID_22289813,Human_RBP_ID_27065044 Human_Splice_Rec_538306,Human_Splice_Rec_538384,Human_Splice_Rec_538426,Human_Splice_Rec_538466,Human_Splice_Rec_538532,Human_Splice_Rec_538576,Human_Splice_Rec_538666,Human_Splice_Rec_538708,Human_Splice_Rec_538724 Human_miRNA_ID_2271719,Human_miRNA_ID_2271720 RMVar_hsa_circ_119169,RMVar_hsa_circ_224294,RMVar_hsa_circ_377664,RMVar_hsa_circ_224319 111060 RMVar_ID_111060 Human_SNP_ID_851855321 m1A Human chr4 - 76195866 76195866 76195866 CATTTTTGTAAATCTCCTTTTGGTTTTTTCCTAGAAAATTGTGTTAAGGAATGGTACTGAGGCAT CATTTTTGTAAATCTCCTTTTGGTTTTTTCCTCGAAAATTGTGTTAAGGAATGGTACTGAGGCAT T G SCARB2 Ensembl:ENSG00000138760 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:76195826..76195875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_104275,RMVar_hsa_circ_226692 111061 RMVar_ID_111061 Human_SNP_ID_851937207 m1A Human chr4 + 1767824 1767824 1767824 CCAGCAGCGGCCCGGAGCTGCCCTTTGTGCAGAGCTGGGGCGGCCCGTACCGTCGTGCCCTTCGG CCAGCAGCGGCCCGGAGCTGCCCTTTGTGCAGGGCTGGGGCGGCCCGTACCGTCGTGCCCTTCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1767775..1767879 26863196 MeRIP-seq:(Medium) rs543504821 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111062 RMVar_ID_111062 Human_SNP_ID_852019640 m1A Human chr4 + 108762955 108762955 108762955 AAGGTGCAAGGTGCAAGGTCTGCGCGCCTCCTACGCGAGCCTGGGACTGCCTTGGCGGCCCCGGC AAGGTGCAAGGTGCAAGGTCTGCGCGCCTCCTGCGCGAGCCTGGGACTGCCTTGGCGGCCCCGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:108762908..108763060 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 111063 RMVar_ID_111063 Human_SNP_ID_852034400 m1A Human chr4 - 1171379 1171379 1171379 AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGATCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG AGCGCGGCGAGGCCTGGGCGCTGATGAAGGAGTTCGAGGCGGCGGGGGAGGCGCTGCAGAGCGTG T A SPON2 Ensembl:ENSG00000159674 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:1171331..1171411;chr4:1171328..1171422 26863196 MeRIP-seq:(Medium) rs749838094 Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_22770925 RMVar_hsa_circ_80155,RMVar_hsa_circ_224229 111064 RMVar_ID_111064 Human_SNP_ID_852183887 m1A Human chr4 - 169753837 169753837 169753837 TTTGGAGAACTAAAGTTTGTGTGCCAATTTTCAGTGTGAAAAAACAACTGATGTGAAGAAAAGTA TTTGGAGAACTAAAGTTTGTGTGCCAATTTTCTGTGTGAAAAAACAACTGATGTGAAGAAAAGTA T A HPF1 Ensembl:ENSG00000056050 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:169753792..169753890 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain 111065 RMVar_ID_111065 Human_SNP_ID_852211914 m1A Human chr4 + 15703885 15703885 15703885 GAGGGGTGTGTGCATGTGTGTTCTAGAGGTGAAGGGGGTGTGTGTGCGTGCGCTCTAGAGGTGAG GAGGGGTGTGTGCATGTGTGTTCTAGAGGTGAGGGGGGTGTGTGTGCGTGCGCTCTAGAGGTGAG A G FAM200B,BST1 Ensembl:ENSG00000237765,Ensembl:ENSG00000109743 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:15703802..15703965 26863196 MeRIP-seq:(Medium) rs1301492883 Functional Loss SNV ICGC 33..33 33 CLLE 1 - 111066 RMVar_ID_111066 Human_SNP_ID_852249523 m1A Human chr4 + 2262059 2262059 2262059 CGGCCCGCTCCGGCCGGCTCCGCTCGCCGCCCACCCCGCGCGCCCGGCCGCCGCACTTCCAGACT CGGCCCGCTCCGGCCGGCTCCGCTCGCCGCCCCCCCCGCGCGCCCGGCCGCCGCACTTCCAGACT A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Starvation treatment;HEK293T,untreat control chr4:2261901..2262125;chr4:2261726..2262125;chr4:2261970..2262100;chr4:2261964..2262078 26863196,26863410,26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,ovary mixed_adenosquamous_carcinoma 2 ovary 111067 RMVar_ID_111067 Human_SNP_ID_852276452 m1A Human chr4 - 2950104 2950102 2950104 AGAAGGTGACAGTTCAGGCGGGGAGGACACAGAGGAGAGCGACAGCCCAGATAGCCACTTGGACC AGAAGGTGACAGTTCAGGCGGGGAGGACACAG__GAGAGCGACAGCCCAGATAGCCACTTGGACC CCT C NOP14 Ensembl:ENSG00000087269 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:2949926..2950200;chr4:2949926..2951250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 COCA 1 - Human_RBP_ID_70853,Human_RBP_ID_248843,Human_RBP_ID_7304257,Human_RBP_ID_8881900,Human_RBP_ID_9304305,Human_RBP_ID_9396118,Human_RBP_ID_21989272,Human_RBP_ID_24547644,Human_RBP_ID_26348875,Human_RBP_ID_27823967 Human_miRNA_ID_2552996 RMVar_hsa_circ_55392,RMVar_hsa_circ_55693,RMVar_hsa_circ_57701,RMVar_hsa_circ_62093,RMVar_hsa_circ_321141,RMVar_hsa_circ_326899,RMVar_hsa_circ_224425,RMVar_hsa_circ_286541,RMVar_hsa_circ_8626,RMVar_hsa_circ_363609,RMVar_hsa_circ_366233,RMVar_hsa_circ_324337,RMVar_hsa_circ_224427,RMVar_hsa_circ_65279,RMVar_hsa_circ_224426 111068 RMVar_ID_111068 Human_SNP_ID_852279130 m1A Human chr4 - 103198349 103198349 103198349 CCCTGAAGTGCCGGCCGCGGAGGGTCCTGGCCATTTTCCTGGGACCAGTTCAGCCTGATAGGATG CCCTGAAGTGCCGGCCGCGGAGGGTCCTGGCCTTTTTCCTGGGACCAGTTCAGCCTGATAGGATG T A CENPE Ensembl:ENSG00000138778 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:103198236..103198371 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_8882172,Human_RBP_ID_9304207,Human_RBP_ID_18424617 Human_Splice_Rec_588341,Human_Splice_Rec_588433,Human_Splice_Rec_588529,Human_Splice_Rec_588633 111069 RMVar_ID_111069 Human_SNP_ID_852296189 m1A Human chr4 + 184010872 184010872 184010872 TCGGGAGGAGTGGCTGAAGGGATCGCCAACGGACGCCTCGTCCAGCACCATGGTGCCGAGCCCAG TCGGGAGGAGTGGCTGAAGGGATCGCCAACGGCCGCCTCGTCCAGCACCATGGTGCCGAGCCCAG A C STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:184010822..184010922 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary RMVar_hsa_circ_229755,RMVar_hsa_circ_229754,RMVar_hsa_circ_294964,RMVar_hsa_circ_277715 111070 RMVar_ID_111070 Human_SNP_ID_852307608 m1A Human chr4 - 173332083 173332083 173332083 GAAGATGAGGAGGAAGAGGATGAAGATGAAGAATAAATGGCTATCCTTTAATGATGCGTGTGGAA GAAGATGAGGAGGAAGAGGATGAAGATGAAGATTAAATGGCTATCCTTTAATGATGCGTGTGGAA T A HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:173331926..173332259 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_12198,Human_RBP_ID_71960,Human_RBP_ID_213212,Human_RBP_ID_616761,Human_RBP_ID_941783,Human_RBP_ID_1636466,Human_RBP_ID_1974756,Human_RBP_ID_3733074,Human_RBP_ID_4798048,Human_RBP_ID_5210755,Human_RBP_ID_5475893,Human_RBP_ID_5531486,Human_RBP_ID_7287802,Human_RBP_ID_8265740,Human_RBP_ID_9152988,Human_RBP_ID_9396781,Human_RBP_ID_15096335,Human_RBP_ID_17296123,Human_RBP_ID_17662031,Human_RBP_ID_18022065,Human_RBP_ID_18413494,Human_RBP_ID_18536957,Human_RBP_ID_18544846,Human_RBP_ID_18820806,Human_RBP_ID_21989364,Human_RBP_ID_22095735,Human_RBP_ID_22510448,Human_RBP_ID_23034743,Human_RBP_ID_23116061,Human_RBP_ID_23120106,Human_RBP_ID_24045074,Human_RBP_ID_24547740,Human_RBP_ID_25791673,Human_RBP_ID_26348932,Human_RBP_ID_27064096,Human_RBP_ID_27507169,Human_RBP_ID_27824529 RMVar_hsa_circ_86542,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577,RMVar_hsa_circ_229578 111071 RMVar_ID_111071 Human_SNP_ID_852310015 m1A Human chr4 + 102826625 102826625 102826625 GCAGGATTGTCTCGTCTCACACCAGCTCTGCCAGACACAGGCGCCTTTTGCAAAAACGGAGCAGA GCAGGATTGTCTCGTCTCACACCAGCTCTGCCTGACACAGGCGCCTTTTGCAAAAACGGAGCAGA A T UBE2D3-AS1,UBE2D3-AS1:2 RNACentral:URS00009B2292,RNACentral:URS00008C092D lincRNA,lincRNA exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:102826501..102826685 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 11 stomach 111072 RMVar_ID_111072 Human_SNP_ID_852321891 m1A Human chr4 - 82356852 82356852 82356852 AGTAGCCATGTCGAAGGAACAATATCAGCAACAGCAACAGTGGGGATCTAGAGGAGGATTTGCAG AGTAGCCATGTCGAAGGAACAATATCAGCAACTGCAACAGTGGGGATCTAGAGGAGGATTTGCAG T A HNRNPD Ensembl:ENSG00000138668 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:82356589..82356915;chr4:82356651..82356900;chr4:82356776..82356900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_249004,Human_RBP_ID_625354,Human_RBP_ID_1037412,Human_RBP_ID_1981403,Human_RBP_ID_2860787,Human_RBP_ID_3744388,Human_RBP_ID_7331669,Human_RBP_ID_9396486,Human_RBP_ID_15208229,Human_RBP_ID_17030756,Human_RBP_ID_17295453,Human_RBP_ID_17408975,Human_RBP_ID_17706272,Human_RBP_ID_18537053,Human_RBP_ID_18826891,Human_RBP_ID_22826548,Human_RBP_ID_26349410,Human_RBP_ID_26517353,Human_RBP_ID_27070612,Human_RBP_ID_27824242 Human_Splice_Rec_573816,Human_Splice_Rec_573817,Human_Splice_Rec_573824,Human_Splice_Rec_573834,Human_Splice_Rec_573835,Human_Splice_Rec_573844,Human_Splice_Rec_573845,Human_Splice_Rec_573858,Human_Splice_Rec_573859,Human_Splice_Rec_573866,Human_Splice_Rec_573867,Human_Splice_Rec_573874,Human_Splice_Rec_573875,Human_Splice_Rec_573888,Human_Splice_Rec_573889 RMVar_hsa_circ_3832,RMVar_hsa_circ_226956,RMVar_hsa_circ_320661,RMVar_hsa_circ_226957,RMVar_hsa_circ_344031,RMVar_hsa_circ_30856,RMVar_hsa_circ_226958,RMVar_hsa_circ_305869 111073 RMVar_ID_111073 Human_SNP_ID_852351554 m1A Human chr4 + 898068 898068 898068 TTCCTCCACCAGGGCTCGCCTCTGGGCGCTCCAGCTGTAGTCAGGGTAGTGCGAGATGGTCGTGG TTCCTCCACCAGGGCTCGCCTCTGGGCGCTCCGGCTGTAGTCAGGGTAGTGCGAGATGGTCGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:896543..898070 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 111074 RMVar_ID_111074 Human_SNP_ID_852468418 m1A Human chr4 - 163166378 163166378 163166378 GGCGCCGGACTCCTTGGAGACCTCGGACTCGGATTCGGACTCGGACAGGTCGGGTGCCTAAGGGA GGCGCCGGACTCCTTGGAGACCTCGGACTCGGGTTCGGACTCGGACAGGTCGGGTGCCTAAGGGA T C NAF1 Ensembl:ENSG00000145414 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:163166375..163166772 32194978 MeRIP-seq:(Medium) rs1173616911 Functional Loss SNV ICGC,COSMIC 33..33 33 LUAD,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_1636148,Human_RBP_ID_8878005 Human_Splice_Rec_619903,Human_Splice_Rec_619917,Human_Splice_Rec_619933,Human_Splice_Rec_619945 111075 RMVar_ID_111075 Human_SNP_ID_852543254 m1A Human chr4 + 153344738 153344738 153344738 GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCATGGTAAGGACTGAGGCTACGGTCCCGCGTCTT GCCCGGCCAGCGGAAGCCCCTGCGCCCGCGCCTTGGTAAGGACTGAGGCTACGGTCCCGCGTCTT A T MND1 Ensembl:ENSG00000121211 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:153344673..153344795 26863196 MeRIP-seq:(Medium) rs750080695 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_4795166,Human_RBP_ID_18424821,Human_RBP_ID_19121868 Human_Splice_Rec_616341,Human_Splice_Rec_616353,Human_Splice_Rec_616357,Human_Splice_Rec_616375 111076 RMVar_ID_111076 Human_SNP_ID_852565876 m1A Human chr4 + 13601197 13601197 13601197 ACCACAGTACCAATCTGACTGTCCCCTTCTGCACTTTCACAAATCAAGACCCCTTCACTTTCTTC ACCACAGTACCAATCTGACTGTCCCCTTCTGCCCTTTCACAAATCAAGACCCCTTCACTTTCTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:13601146..13601374 26863196 MeRIP-seq:(Medium) rs763935230 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue 111077 RMVar_ID_111077 Human_SNP_ID_852627600 m1A Human chr4 - 967804 967804 967804 CACTGAATGAGGGGTCCGTGTGCCCGACCCGCAGGCGAGGGGGGCGACGGCGCCGACGGGAGCGC CACTGAATGAGGGGTCCGTGTGCCCGACCCGCCGGCGAGGGGGGCGACGGCGCCGACGGGAGCGC T G DGKQ Ensembl:ENSG00000145214 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:967791..967881 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_19121979 Human_Splice_Rec_536491,Human_Splice_Rec_536535 RMVar_hsa_circ_38065,RMVar_hsa_circ_224219 111078 RMVar_ID_111078 Human_SNP_ID_852635207 m1A Human chr4 - 49092882 49092882 49092882 AATGGAATGGAATGGAATGGAGTGGAATCAACACGAATGGAAAGGAACGGAATGGAATGGAATGC AATGGAATGGAATGGAATGGAGTGGAATCAACCCGAATGGAAAGGAACGGAATGGAATGGAATGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49092817..49092946 26863196 MeRIP-seq:(Medium) rs371292158 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111079 RMVar_ID_111079 Human_SNP_ID_852646269 m1A Human chr4 - 40816261 40816261 40816261 TAATTACCTTAAAACACGTTTTGTTTTATTTCAGTTACGATATCAGAAGTGCTTGGTAGCCAGGC TAATTACCTTAAAACACGTTTTGTTTTATTTCTGTTACGATATCAGAAGTGCTTGGTAGCCAGGC T A APBB2 Ensembl:ENSG00000163697 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:40816226..40816275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111080 RMVar_ID_111080 Human_SNP_ID_852660979 m1A Human chr4 - 10116544 10116544 10116544 TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGAGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG TGCGGGTGGCGGGGGAGTCCTCGGCGCGGGGGGGGGGTGCGGGCGCCGGCCGGAGGCGTGGCGGG T C WDR1 Ensembl:ENSG00000071127 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:10116542..10116800 26863196 MeRIP-seq:(Medium) rs908488610 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_939606,Human_RBP_ID_5326356,Human_RBP_ID_5394002,Human_RBP_ID_9334641,Human_RBP_ID_19122297,Human_RBP_ID_22679053,Human_RBP_ID_26791217 RMVar_hsa_circ_122269,RMVar_hsa_circ_224834,RMVar_hsa_circ_77371,RMVar_hsa_circ_224841,RMVar_hsa_circ_112385,RMVar_hsa_circ_224847,RMVar_hsa_circ_83464,RMVar_hsa_circ_224850 111081 RMVar_ID_111081 Human_SNP_ID_852734473 m1A Human chr4 + 6783601 6783600 6783601 CCAGCATTGTCCTTTTGGGGCCCCGGGAAGGGAAAACCGCCGGGCGGGGGAGGAGGGCCGCAGGC CCAGCATTGTCCTTTTGGGGCCCCGGGAAGGG_AAACCGCCGGGCGGGGGAGGAGGGCCGCAGGC GA G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:6783593..6783745 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 MALY 1 - Human_RBP_ID_3747313,Human_RBP_ID_5089918,Human_RBP_ID_8129871 111082 RMVar_ID_111082 Human_SNP_ID_852737969 m1A Human chr4 - 176320110 176320110 176320110 GAGCGCCGCCATCACGCTCAGCGAGAAGGCGAACAGTGAGTTCGCCCGCGACAGCACCGTGTTCA GAGCGCCGCCATCACGCTCAGCGAGAAGGCGATCAGTGAGTTCGCCCGCGACAGCACCGTGTTCA T A AC019163.1 Ensembl:ENSG00000248980 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:176320009..176320113 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 111083 RMVar_ID_111083 Human_SNP_ID_852744545 m1A Human chr4 + 56316101 56316098 56316101 TGCGCTTCAACTGCGACCAACAGGCAGAACAGAAGAAGAAGAAGAGGCACAGCAGCACCGGAGAC TGCGCTTCAACTGCGACCAACAGGCAGAAC___AGAAGAAGAAGAGGCACAGCAGCACCGGAGAC CAGA C CRACD Ensembl:ENSG00000109265 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:56316050..56316484 26863196 MeRIP-seq:(Medium) rs748490494 Functional Loss DEL TCGA,ICGC 31..33 33 STAD,UCEC 2 - RMVar_hsa_circ_302627,RMVar_hsa_circ_266430,RMVar_hsa_circ_30363,RMVar_hsa_circ_226214,RMVar_hsa_circ_226215 111084 RMVar_ID_111084 Human_SNP_ID_852787616 m1A Human chr4 + 99076472 99076472 99076472 TTATTGATGTCCACACCAATGATCCGGGAAGCACCAGCCACTTTACAGCCCATGATAACTGCCAA TTATTGATGTCCACACCAATGATCCGGGAAGCCCCAGCCACTTTACAGCCCATGATAACTGCCAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99076351..99076831 32194978 MeRIP-seq:(Medium) rs199508117 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,oesophagus squamous_cell_carcinoma 4 oesophagus 111085 RMVar_ID_111085 Human_SNP_ID_852865031 m1A Human chr4 + 169122262 169122261 169122263 CCAGGAGAGGGGGTGGTGGAAGAGGAGGATTCAAAGTCTAGTATAGGAAAAACATAAAGAGAAAG CCAGGAGAGGGGGTGGTGGAAGAGGAGGATTC__AGTCTAGTATAGGAAAAACATAAAGAGAAAG CAA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:169122220..169122307 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 UCEC 1 - 111086 RMVar_ID_111086 Human_SNP_ID_852927832 m1A Human chr4 - 56315808 56315808 56315808 GGTGCATCTCCGACTTCTCCGGACCCTTCCCGAGCTCGCGAACACCAGCAGGAGGAGGCTGGGGG GGTGCATCTCCGACTTCTCCGGACCCTTCCCGGGCTCGCGAACACCAGCAGGAGGAGGCTGGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:56315758..56315849 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung 111087 RMVar_ID_111087 Human_SNP_ID_852987633 m1A Human chr4 + 1822306 1822306 1822306 TTGGGGAGCAGCTACCACACGTTCGGGCTCAAAATCCTTCTGAAAGGCAAGGCGACACCAGCCCA TTGGGGAGCAGCTACCACACGTTCGGGCTCAACATCCTTCTGAAAGGCAAGGCGACACCAGCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:1822201..1822347 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 111088 RMVar_ID_111088 Human_SNP_ID_852996991 m1A Human chr4 - 8592847 8592847 8592847 CGACGACCAGGACTGTAAGGAGCAGCAGCGGCAGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG CGACGACCAGGACTGTAAGGAGCAGCAGCGGCGGCGGGGGCGGCATGGTGGGGCGGCGGACCTTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:8592800..8592910 26863196 MeRIP-seq:(Medium) rs2302583 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,caecum adenocarcinoma,COCA,central_nervous_system oligodendroglioma_Grade_III,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma,frontal_lobe oligodendroglioma_Grade_III 77 caecum,head and neck,large intestine,brain 111089 RMVar_ID_111089 Human_SNP_ID_852999688 m1A Human chr4 - 99082017 99082017 99082017 TTCCAGTGATCTTGGGACATGAAGGTGCTGGAATTGTGGAAAGTGTTGGTGAGGGAGTTACTAAG TTCCAGTGATCTTGGGACATGAAGGTGCTGGACTTGTGGAAAGTGTTGGTGAGGGAGTTACTAAG T G ADH5 Ensembl:ENSG00000197894 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:99081954..99085201 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_609848,Human_RBP_ID_941408,Human_RBP_ID_1971004,Human_RBP_ID_5121051,Human_RBP_ID_5394402,Human_RBP_ID_9147909,Human_RBP_ID_18032681,Human_RBP_ID_19013871,Human_RBP_ID_22457720 Human_Splice_Rec_585136,Human_Splice_Rec_585137,Human_Splice_Rec_585164,Human_Splice_Rec_585165,Human_Splice_Rec_585188,Human_Splice_Rec_585189,Human_Splice_Rec_585196,Human_Splice_Rec_585197,Human_Splice_Rec_585206,Human_Splice_Rec_585207,Human_Splice_Rec_585216,Human_Splice_Rec_585217,Human_Splice_Rec_585228,Human_Splice_Rec_585229,Human_Splice_Rec_585238,Human_Splice_Rec_585239,Human_Splice_Rec_585246,Human_Splice_Rec_585252 RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 111090 RMVar_ID_111090 Human_SNP_ID_853007992 m1A Human chr4 + 24325718 24325718 24325718 CCGATCGCCTCGGAAGCCCCGTAGACCACCACAGATGCCGAGCTTTGAGTAACTCTCACAGTGGA CCGATCGCCTCGGAAGCCCCGTAGACCACCACGGATGCCGAGCTTTGAGTAACTCTCACAGTGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:24325620..24325724 26863196 MeRIP-seq:(Medium) rs538183543 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_2843053 111091 RMVar_ID_111091 Human_SNP_ID_853051616 m1A Human chr4 + 41935472 41935472 41935472 TCTCTCTTCGCGGTTGCGGCGTCGCAGACGCTAGTGTGAGCCCCCATGGCAGATACGACCCCGAA TCTCTCTTCGCGGTTGCGGCGTCGCAGACGCTCGTGTGAGCCCCCATGGCAGATACGACCCCGAA A C TMEM33 Ensembl:ENSG00000109133 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr4:41935151..41938641;chr4:41935183..41935474 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_70874,Human_RBP_ID_4794597,Human_RBP_ID_9334682,Human_RBP_ID_18026376,Human_RBP_ID_22457677,Human_RBP_ID_24055652,Human_RBP_ID_24430634 Human_Splice_Rec_557285,Human_Splice_Rec_557298,Human_Splice_Rec_557299,Human_Splice_Rec_557311,Human_Splice_Rec_557321,Human_Splice_Rec_557333,Human_Splice_Rec_557337,Human_Splice_Rec_557349 Human_miRNA_ID_2449814 RMVar_hsa_circ_9786,RMVar_hsa_circ_77638,RMVar_hsa_circ_225689 111092 RMVar_ID_111092 Human_SNP_ID_853083737 m1A Human chr4 + 13627540 13627540 13627540 GGCGGTGGCTGCGGCTGCGGCTGCGGCGGGGGAGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG GGCGGTGGCTGCGGCTGCGGCTGCGGCGGGGGGGGCGGCGGCGCCGGAGGAGGCGGCTGCGGCTG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:13627476..13627700 26863196 MeRIP-seq:(Medium) rs945329219 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111093 RMVar_ID_111093 Human_SNP_ID_853095581 m1A Human chr4 - 25914387 25914387 25914387 ACTCCTCCAATCTCATTAGGGGCCGGAAGTAGATGGGATAGAAGGCGGCGCCGATCAGGGAGATG ACTCCTCCAATCTCATTAGGGGCCGGAAGTAGGTGGGATAGAAGGCGGCGCCGATCAGGGAGATG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:25914249..25914401 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney 111094 RMVar_ID_111094 Human_SNP_ID_853102462 m1A Human chr4 + 1671385 1671385 1671385 CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCACCAGCTCACAGCCACGGCCCGGACTCACCTCT CCCGGACTCACCTCTGTCCCAGCGTCAGAGCCCCCAGCTCACAGCCACGGCCCGGACTCACCTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:1670835..1671435;chr4:1670890..1671458 26863196 MeRIP-seq:(Medium) rs28458319 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111095 RMVar_ID_111095 Human_SNP_ID_853140748 m1A Human chr4 - 49648693 49648683 49648693 CCGTTCCTTTCCATTCCATTCCATTCCATTCCATTCCGTTCCGTTCCATTCCATTCGTGTTGATT CCGTTCCTTTCCATTCCATTCCATTCCATTCC__________GTTCCATTCCATTCGTGTTGATT CGGAACGGAAT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49648613..49648770 26863196 MeRIP-seq:(Medium) rs202099456 Functional Loss DEL ICGC 33..42 33 PBCA 1 - 111096 RMVar_ID_111096 Human_SNP_ID_853290888 m1A Human chr4 + 2831975 2831975 2831975 CTTCGTCAACACCACGGAGTCCTGCGAAGTGGAAAGGTCAGCACAAAGCCCTGTGTGTGCTGGGT CTTCGTCAACACCACGGAGTCCTGCGAAGTGGGAAGGTCAGCACAAAGCCCTGTGTGTGCTGGGT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2831598..2831991 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 8 kidney Human_RBP_ID_19121430 Human_Splice_Rec_540055,Human_Splice_Rec_540161,Human_Splice_Rec_540193,Human_Splice_Rec_540223,Human_Splice_Rec_540245,Human_Splice_Rec_540285,Human_Splice_Rec_540295 RMVar_hsa_circ_9936,RMVar_hsa_circ_89980,RMVar_hsa_circ_96867,RMVar_hsa_circ_112687,RMVar_hsa_circ_224396,RMVar_hsa_circ_224397,RMVar_hsa_circ_224398 111097 RMVar_ID_111097 Human_SNP_ID_853360511 m1A Human chr4 + 13603704 13603704 13603704 TCCTCTCCGATTTTCGCACAACCTTCTACTTAATTTCTTTTCCATGAGTGAACTATTACCTCTGG TCCTCTCCGATTTTCGCACAACCTTCTACTTACTTTCTTTTCCATGAGTGAACTATTACCTCTGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:13603653..13603742 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 111098 RMVar_ID_111098 Human_SNP_ID_853402986 m1A Human chr4 - 56068151 56068151 56068151 TCTCAGAGACGCTGTTCCTGACCATCCTATCCAAAGCCACCACCACCACCATCTTCCCAACCTCC TCTCAGAGACGCTGTTCCTGACCATCCTATCCTAAGCCACCACCACCACCATCTTCCCAACCTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:56068150..56068274 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 111099 RMVar_ID_111099 Human_SNP_ID_853403269 m1A Human chr4 - 107989924 107989924 107989924 GAACTGCCTGGTGACGAAGGCCATGGTGTGGCAGCGGCGGCGACAGCGAGGAGACCCGGGCAGGG GAACTGCCTGGTGACGAAGGCCATGGTGTGGCGGCGGCGGCGACAGCGAGGAGACCCGGGCAGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:107989873..107990008 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 111100 RMVar_ID_111100 Human_SNP_ID_853437394 m1A Human chr4 - 108009761 108009761 108009761 ACCAACACTACTGTGTGACCAGTTGCTGCAGCAACCTAGAGCAACAAAAGAACAATTTCTTTTTA ACCAACACTACTGTGTGACCAGTTGCTGCAGCTACCTAGAGCAACAAAAGAACAATTTCTTTTTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:108009751..108009775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 8 stomach 111101 RMVar_ID_111101 Human_SNP_ID_853505297 m1A Human chr4 - 73258325 73258325 73258325 CGGAGGTGGCGGCGGCGGCACCAGCAGTAACAACAGCGAGGAAGAAGAGGACGACGACGACGAGG CGGAGGTGGCGGCGGCGGCACCAGCAGTAACAGCAGCGAGGAAGAAGAGGACGACGACGACGAGG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:73258205..73258800 26863196 MeRIP-seq:(Medium) rs906955660 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_71358,Human_RBP_ID_248983,Human_RBP_ID_838045,Human_RBP_ID_2856240,Human_RBP_ID_4789930,Human_RBP_ID_9396394,Human_RBP_ID_23034914,Human_RBP_ID_25835636,Human_RBP_ID_26349363,Human_RBP_ID_27824200 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 111102 RMVar_ID_111102 Human_SNP_ID_853509348 m1A Human chr4 + 56441664 56441664 56441664 ATTTTGGTCTATTTCCATTTTATTTCCACAGTACTGAACATTGGTAAAAAATTATATGAGGGTAA ATTTTGGTCTATTTCCATTTTATTTCCACAGTGCTGAACATTGGTAAAAAATTATATGAGGGTAA A G PAICS Ensembl:ENSG00000128050 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:56441651..56441675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_4794971,Human_RBP_ID_22458595,Human_RBP_ID_23033026 Human_Splice_Rec_563294,Human_Splice_Rec_563312,Human_Splice_Rec_563330,Human_Splice_Rec_563346,Human_Splice_Rec_563348,Human_Splice_Rec_563350,Human_Splice_Rec_563368 RMVar_hsa_circ_55288,RMVar_hsa_circ_336530 111103 RMVar_ID_111103 Human_SNP_ID_853534494 m1A Human chr4 - 1801686 1801686 1801686 CCGGATGCTGCCAAACTTGTTCTCCACGACGCAGGTGTAGTTGCCGCGGTCCGAGGGCACCACGC CCGGATGCTGCCAAACTTGTTCTCCACGACGCGGGTGTAGTTGCCGCGGTCCGAGGGCACCACGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1793951..1801931 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 12 large intestine 111104 RMVar_ID_111104 Human_SNP_ID_853725658 m1A Human chr4 - 139124151 139124151 139124151 CAGCCAAGCTGGGTGTGGTGGTGTGCATCTGTACTCCCAGCTACTTGGGAGACTGGGGCAGGTGG CAGCCAAGCTGGGTGTGGTGGTGTGCATCTGTGCTCCCAGCTACTTGGGAGACTGGGGCAGGTGG T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:139124146..139124225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_228676,RMVar_hsa_circ_12262,RMVar_hsa_circ_96628,RMVar_hsa_circ_228670,RMVar_hsa_circ_228667,RMVar_hsa_circ_365851,RMVar_hsa_circ_228674,RMVar_hsa_circ_288745,RMVar_hsa_circ_366492,RMVar_hsa_circ_228682,RMVar_hsa_circ_81011,RMVar_hsa_circ_47514,RMVar_hsa_circ_269030,RMVar_hsa_circ_318390,RMVar_hsa_circ_228680,RMVar_hsa_circ_228684,RMVar_hsa_circ_278299,RMVar_hsa_circ_333983,RMVar_hsa_circ_228681,RMVar_hsa_circ_296032,RMVar_hsa_circ_228685,RMVar_hsa_circ_228683 111105 RMVar_ID_111105 Human_SNP_ID_853733095 m1A Human chr4 - 109816195 109816195 109816195 GTTGAAGCCGCCACCTCCACCACCTCGATTAAAGCCTCCACGACCTCCGCCTCGAAAAGACATTC GTTGAAGCCGCCACCTCCACCACCTCGATTAACGCCTCCACGACCTCCGCCTCGAAAAGACATTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:109815701..109816350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 111106 RMVar_ID_111106 Human_SNP_ID_853741846 m1A Human chr4 + 2251182 2251182 2251182 GCACCGACAGCTGCTCCAGGCGCCGCTTCAGGAAACGATGCTCCTGCTGCAGCTGCTCCTTGATG GCACCGACAGCTGCTCCAGGCGCCGCTTCAGGGAACGATGCTCCTGCTGCAGCTGCTCCTTGATG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:2250661..2252553 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111107 RMVar_ID_111107 Human_SNP_ID_853772762 m1A Human chr4 + 759952 759952 759952 CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCACGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC CTTCTCCTTCCGGACTCCGGGTCTTTCTCCCCGCGGCCTCTCTCCCGAGTTCTCTCTCCAGACTC A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:759947..760077 26863196 MeRIP-seq:(Medium) rs796077687 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_18955021,Human_RBP_ID_21064190 RMVar_hsa_circ_31864,RMVar_hsa_circ_37697,RMVar_hsa_circ_345456,RMVar_hsa_circ_319968,RMVar_hsa_circ_323026,RMVar_hsa_circ_345788 111108 RMVar_ID_111108 Human_SNP_ID_853776524 m1A Human chr4 - 118279068 118279068 118279068 CACAAGAGCGACAGAGTAGACTCAAGATGGCCACATGACACAGACGGCTGAACAGGCTTCACCGG CACAAGAGCGACAGAGTAGACTCAAGATGGCCGCATGACACAGACGGCTGAACAGGCTTCACCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:118278805..118279125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_228190,RMVar_hsa_circ_228191 111109 RMVar_ID_111109 Human_SNP_ID_853825375 m1A Human chr4 - 183495364 183495364 183495364 CTGACATGAATAATGGCCTGGGGGAGAGGGGGAGAGAAGCAAGAGAAAGGAGCAGTTAAGAGGAA CTGACATGAATAATGGCCTGGGGGAGAGGGGGTGAGAAGCAAGAGAAAGGAGCAGTTAAGAGGAA T A AC107214.1 Ensembl:ENSG00000232648 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:183495315..183495401 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111110 RMVar_ID_111110 Human_SNP_ID_853841564 m1A Human chr4 + 70689270 70689270 70689270 GGCCTTTGCAAAACCAGTGCCTCAGGTAGATGAGGCTGAGACACGGGTCGTGAAGGATTTGGCTA GGCCTTTGCAAAACCAGTGCCTCAGGTAGATGGGGCTGAGACACGGGTCGTGAAGGATTTGGCTA A G UTP3 Ensembl:ENSG00000132467 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr4:70689169..70689318 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_1640046,Human_RBP_ID_8880756 RMVar_hsa_circ_226451 111111 RMVar_ID_111111 Human_SNP_ID_853855222 m1A Human chr4 + 147481200 147481200 147481200 GGGGATTGGGGTCCCAGCGAGACCTCCCCGGGAGAAGCAGTGCCCAGGAGGTTTTCTGAAGCCGG GGGGATTGGGGTCCCAGCGAGACCTCCCCGGGTGAAGCAGTGCCCAGGAGGTTTTCTGAAGCCGG A T EDNRA Ensembl:ENSG00000151617 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:147481028..147481285 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 111112 RMVar_ID_111112 Human_SNP_ID_853885413 m1A Human chr4 - 342939 342939 342939 AAAAATAAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT AAAAATAAGGTCTCAGCCTTGGATCAGGAGATTATTGAAGTAGATCCTGACACTAAGGAAATGCT T A AC079140.2 Ensembl:ENSG00000250321 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879960082 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_18408892 111113 RMVar_ID_111113 Human_SNP_ID_853947591 m1A Human chr4 - 169561556 169561556 169561556 GAAATGGTGTTTTGTTTATTTCTTTTCCCCAAAGTTGGAAAGAATAAATAGGGCCAGGGAACAAG GAAATGGTGTTTTGTTTATTTCTTTTCCCCAACGTTGGAAAGAATAAATAGGGCCAGGGAACAAG T G NEK1 Ensembl:ENSG00000137601 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr4:169561531..169561599;chr4:169561522..169561693 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_2832438,Human_RBP_ID_3732810 Human_Splice_Rec_622013,Human_Splice_Rec_622103,Human_Splice_Rec_622169,Human_Splice_Rec_622233,Human_Splice_Rec_622351 RMVar_hsa_circ_66227,RMVar_hsa_circ_57562,RMVar_hsa_circ_66616,RMVar_hsa_circ_122853,RMVar_hsa_circ_229505,RMVar_hsa_circ_18632,RMVar_hsa_circ_69567,RMVar_hsa_circ_365739,RMVar_hsa_circ_73308,RMVar_hsa_circ_354376,RMVar_hsa_circ_69461,RMVar_hsa_circ_324547,RMVar_hsa_circ_326220,RMVar_hsa_circ_10925,RMVar_hsa_circ_38601,RMVar_hsa_circ_29311,RMVar_hsa_circ_229524,RMVar_hsa_circ_229525,RMVar_hsa_circ_266448,RMVar_hsa_circ_352779,RMVar_hsa_circ_360661,RMVar_hsa_circ_367972,RMVar_hsa_circ_83241,RMVar_hsa_circ_104294,RMVar_hsa_circ_229527,RMVar_hsa_circ_229528,RMVar_hsa_circ_229529,RMVar_hsa_circ_265548,RMVar_hsa_circ_57536,RMVar_hsa_circ_70128,RMVar_hsa_circ_53315,RMVar_hsa_circ_229530 111114 RMVar_ID_111114 Human_SNP_ID_853972132 m1A Human chr4 - 49643589 49643589 49643589 CCATTCCATTCCATTGCATTGCATTTCCTTCCATTCCAGTTGATTCCATTCCATTCCATTCCATT CCATTCCATTCCATTGCATTGCATTTCCTTCCTTTCCAGTTGATTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49643575..49643659 26863196 MeRIP-seq:(Medium) rs1344024133 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111115 RMVar_ID_111115 Human_SNP_ID_854014150 m1A Human chr4 - 183700574 183700574 183700574 CAATTTTATAGCAAATTCCCTGATGACAAGATAAGCGCCCATTCAAACCAAGTCTCCTCCACCTT CAATTTTATAGCAAATTCCCTGATGACAAGATGAGCGCCCATTCAAACCAAGTCTCCTCCACCTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:183700527..183700674 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111116 RMVar_ID_111116 Human_SNP_ID_854022901 m1A Human chr4 + 674224 674224 674224 GGCTGCAAAGCCTGGATCACCTTGATGAGCGGAGAGACCTGCACCGGTGGCACCATCTTGTCCCT GGCTGCAAAGCCTGGATCACCTTGATGAGCGGTGAGACCTGCACCGGTGGCACCATCTTGTCCCT A T MYL5 Ensembl:ENSG00000215375 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:673871..674325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_19121288,Human_RBP_ID_22745637 111117 RMVar_ID_111117 Human_SNP_ID_854104286 m1A Human chr4 + 38014602 38014602 38014602 ACTGCCCGTCCGAGTTCGACGACACGTTTTCCAAGAAGTTCGAGGTGCTCTTCTGCGGCCGCGTG ACTGCCCGTCCGAGTTCGACGACACGTTTTCCGAGAAGTTCGAGGTGCTCTTCTGCGGCCGCGTG A G TBC1D1 Ensembl:ENSG00000065882 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:38014551..38014675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_RBP_ID_4784620,Human_RBP_ID_5475915,Human_RBP_ID_18823823 Human_Splice_Rec_553468,Human_Splice_Rec_553506,Human_Splice_Rec_553564 RMVar_hsa_circ_55582,RMVar_hsa_circ_118649,RMVar_hsa_circ_225338,RMVar_hsa_circ_291800,RMVar_hsa_circ_292011,RMVar_hsa_circ_68161,RMVar_hsa_circ_225339 111118 RMVar_ID_111118 Human_SNP_ID_854109549 m1A Human chr4 - 49648693 49648682 49648693 CCGTTCCTTTCCATTCCATTCCATTCCATTCCATTCCGTTCCGTTCCATTCCATTCGTGTTGATT CCGTTCCTTTCCATTCCATTCCATTCCATTCC___________TTCCATTCCATTCGTGTTGATT ACGGAACGGAAT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49648613..49648770 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..43 33 SKCA 1 - 111119 RMVar_ID_111119 Human_SNP_ID_854125505 m1A Human chr4 - 1918427 1918427 1918427 GGTGACTCTCCAGGGTCTCTGCAGAGCTACACAGTTTGGCCCTCCGCCTTCTCTTCATGGGAATG GGTGACTCTCCAGGGTCTCTGCAGAGCTACACCGTTTGGCCCTCCGCCTTCTCTTCATGGGAATG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1918376..1918575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 16 large intestine 111120 RMVar_ID_111120 Human_SNP_ID_854132723 m1A Human chr4 - 10075034 10075034 10075034 ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTATCTGTCAGGGGAGGTTGTACAGGTGAATGAGC ACAGAGCCCCTGGCCCCGCCGCGGCTCTCACTGTCTGTCAGGGGAGGTTGTACAGGTGAATGAGC T C WDR1 Ensembl:ENSG00000071127 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9732 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_24384755,Human_RBP_ID_26512251 Human_miRNA_ID_1268130 GWAS_ID_9234,GWAS_ID_9235,GWAS_ID_9236,GWAS_ID_9237,GWAS_ID_9238,GWAS_ID_9239,GWAS_ID_9240,GWAS_ID_9241,GWAS_ID_9242,GWAS_ID_9243,GWAS_ID_9244 RMVar_hsa_circ_94689,RMVar_hsa_circ_117277,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224832,RMVar_hsa_circ_224829 111121 RMVar_ID_111121 Human_SNP_ID_854133275 m1A Human chr4 - 164197077 164197077 164197077 AGGGGACGAGGAGGATGAAGAAGGTTATAACGATGGAGAGGTAGATGGCGAGGAAGATGAAGAAG AGGGGACGAGGAGGATGAAGAAGGTTATAACGGTGGAGAGGTAGATGGCGAGGAAGATGAAGAAG T C MARCHF1,ANP32C Ensembl:ENSG00000145416,Ensembl:ENSG00000248546 Protein coding,Pseudogene intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:164197005..164197226 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_1035648 RMVar_hsa_circ_17408 111122 RMVar_ID_111122 Human_SNP_ID_854214873 m1A Human chr4 - 113902981 113902981 113902981 GGGCTGTAGGCTTTGTGCATAGCCCACTTCTGAAAAACAAGGGAACAGTGTGTAAGGAACTTGTG GGGCTGTAGGCTTTGTGCATAGCCCACTTCTGGAAAACAAGGGAACAGTGTGTAAGGAACTTGTG T C ARSJ Ensembl:ENSG00000180801 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:113902930..113903131 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 1 skin,head and neck 111123 RMVar_ID_111123 Human_SNP_ID_854244017 m1A Human chr4 + 38932290 38932290 38932290 AAGTCTGGCGGAGGTAACAGCGCGCTGTATTGAGCAGCTTCATAAAGTAGCAGAATTAATTCTTC AAGTCTGGCGGAGGTAACAGCGCGCTGTATTGGGCAGCTTCATAAAGTAGCAGAATTAATTCTTC A G FAM114A1 Ensembl:ENSG00000197712 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:38929251..38932289 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_213178,Human_RBP_ID_9396253,Human_RBP_ID_26349950 Human_Splice_Rec_554056,Human_Splice_Rec_554057,Human_Splice_Rec_554084,Human_Splice_Rec_554085,Human_Splice_Rec_554098,Human_Splice_Rec_554099 RMVar_hsa_circ_4204,RMVar_hsa_circ_72043,RMVar_hsa_circ_361186,RMVar_hsa_circ_69362,RMVar_hsa_circ_125537,RMVar_hsa_circ_367600,RMVar_hsa_circ_359088,RMVar_hsa_circ_365247,RMVar_hsa_circ_377198,RMVar_hsa_circ_353090,RMVar_hsa_circ_350454,RMVar_hsa_circ_359157,RMVar_hsa_circ_321084,RMVar_hsa_circ_225384,RMVar_hsa_circ_69452,RMVar_hsa_circ_225383 111124 RMVar_ID_111124 Human_SNP_ID_854274459 m1A Human chr4 + 49510607 49510607 49510607 TTCTCTCTTACTCCTTCTGCCCTCTCTCTTTCATATGCCTTAGGTGCATCCCACATTCTGCGTTT TTCTCTCTTACTCCTTCTGCCCTCTCTCTTTCCTATGCCTTAGGTGCATCCCACATTCTGCGTTT A C HSALNG0034347-001 RNACentral:URS0000EBF1A5 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2313294 Functional Loss SNV ICGC 33..33 33 COCA 3 - 111125 RMVar_ID_111125 Human_SNP_ID_854277891 m1A Human chr4 + 182487947 182487947 182487947 TTATAACAGGAATTCTAGAATATGGTGGGTTAAAATAGGAAGTTATGTATGGCAATAATGAGTTT TTATAACAGGAATTCTAGAATATGGTGGGTTACAATAGGAAGTTATGTATGGCAATAATGAGTTT A C TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:182487928..182488011 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_96182,RMVar_hsa_circ_119113,RMVar_hsa_circ_14204,RMVar_hsa_circ_47790,RMVar_hsa_circ_229673,RMVar_hsa_circ_229674,RMVar_hsa_circ_47100,RMVar_hsa_circ_341078,RMVar_hsa_circ_25767 111126 RMVar_ID_111126 Human_SNP_ID_854306438 m1A Human chr4 + 139370313 139370313 139370313 AGAAGAAGAGAAAAAAAATGCAGAAAAAGAAAAGCAGCAGAGAAATCAGAAAAAGAAGAAGGATG AGAAGAAGAGAAAAAAAATGCAGAAAAAGAAAGGCAGCAGAGAAATCAGAAAAAGAAGAAGGATG A G NAA15 Ensembl:ENSG00000164134 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:139370264..139370361 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_72010,Human_RBP_ID_213524,Human_RBP_ID_941024,Human_RBP_ID_17662017,Human_RBP_ID_18818814,Human_RBP_ID_19014591,Human_RBP_ID_24547728,Human_RBP_ID_26350328 Human_Splice_Rec_609517,Human_Splice_Rec_609555 RMVar_hsa_circ_121784,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_22637,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_51640,RMVar_hsa_circ_376577,RMVar_hsa_circ_27237,RMVar_hsa_circ_45370,RMVar_hsa_circ_102608,RMVar_hsa_circ_54256,RMVar_hsa_circ_228706,RMVar_hsa_circ_77949,RMVar_hsa_circ_228705,RMVar_hsa_circ_228707,RMVar_hsa_circ_311357,RMVar_hsa_circ_350026,RMVar_hsa_circ_355480,RMVar_hsa_circ_335029,RMVar_hsa_circ_228708 111127 RMVar_ID_111127 Human_SNP_ID_854424665 m1A Human chr4 - 10087940 10087940 10087940 TGGCACATGACACACTGCTTTTTTCTGAATAGATTAGTTGGAGTCCCGACAGCACCCATTTGCTT TGGCACATGACACACTGCTTTTTTCTGAATAGGTTAGTTGGAGTCCCGACAGCACCCATTTGCTT T C WDR1 Ensembl:ENSG00000071127 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:10087926..10087950 32194978 MeRIP-seq:(Medium) rs763221944 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_22679749 Human_Splice_Rec_545816,Human_Splice_Rec_545836,Human_Splice_Rec_545862,Human_Splice_Rec_545902,Human_Splice_Rec_545920,Human_Splice_Rec_545938,Human_Splice_Rec_545946,Human_Splice_Rec_545954,Human_Splice_Rec_545960,Human_Splice_Rec_545966 RMVar_hsa_circ_8901,RMVar_hsa_circ_127946,RMVar_hsa_circ_122269,RMVar_hsa_circ_224829,RMVar_hsa_circ_16319,RMVar_hsa_circ_71998,RMVar_hsa_circ_224834,RMVar_hsa_circ_48704,RMVar_hsa_circ_113284,RMVar_hsa_circ_224838,RMVar_hsa_circ_336483,RMVar_hsa_circ_358797,RMVar_hsa_circ_377849,RMVar_hsa_circ_92567,RMVar_hsa_circ_224839,RMVar_hsa_circ_224840 111128 RMVar_ID_111128 Human_SNP_ID_854474317 m1A Human chr4 - 163494719 163494719 163494719 TCTCACCAACCGCAGGAGCAGCAGCTCACAAGAGCACCCGGGCCGAATCCCACGTGGCGCCTGAG TCTCACCAACCGCAGGAGCAGCAGCTCACAAGCGCACCCGGGCCGAATCCCACGTGGCGCCTGAG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr4:163494676..163494824;chr4:163494678..163494827 26863196 MeRIP-seq:(Medium) rs561867134 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 111129 RMVar_ID_111129 Human_SNP_ID_854474832 m1A Human chr4 + 39521502 39521502 39521502 CATAGCCTGCACCGATGCAACAGATCTTCTTAATTTCAAACATGATTGTACTAGAAGGAAAACAG CATAGCCTGCACCGATGCAACAGATCTTCTTATTTTCAAACATGATTGTACTAGAAGGAAAACAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:39521451..39526425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111130 RMVar_ID_111130 Human_SNP_ID_854523317 m1A Human chr4 + 2059679 2059679 2059679 CCCGGGCCGGCCGCCGCGCCCCCCGCGCCCCCACCTGCCCCGGTGGCTCAGCCTCACGGCGGGGC CCCGGGCCGGCCGCCGCGCCCCCCGCGCCCCCCCCTGCCCCGGTGGCTCAGCCTCACGGCGGGGC A C NAT8L Ensembl:ENSG00000185818 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr4:2059462..2059772 26863196 MeRIP-seq:(Medium) rs900199956 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung RMVar_hsa_circ_264920 111131 RMVar_ID_111131 Human_SNP_ID_854553329 m1A Human chr4 - 705867 705867 705867 CCCTCTGGGTCCCCCCCAAGAGGAGGAGAAAAAAGCCCGTCCGGAGTTTAAAACAAAGAGGCGGA CCCTCTGGGTCCCCCCCAAGAGGAGGAGAAAATAGCCCGTCCGGAGTTTAAAACAAAGAGGCGGA T A - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr4:705834..705978;chr4:705824..706063 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 111132 RMVar_ID_111132 Human_SNP_ID_854565377 m1A Human chr4 + 1336926 1336926 1336926 ATCCAGCAGTTCCGGTACGACAACTACCGACTACACCAGCTGGGAAACAATTCTGTGTTCACCCT ATCCAGCAGTTCCGGTACGACAACTACCGACTCCACCAGCTGGGAAACAATTCTGTGTTCACCCT A C MAEA Ensembl:ENSG00000090316 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1336876..1336975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_22458086 Human_Splice_Rec_537258,Human_Splice_Rec_537259,Human_Splice_Rec_537286,Human_Splice_Rec_537296,Human_Splice_Rec_537297,Human_Splice_Rec_537312,Human_Splice_Rec_537313,Human_Splice_Rec_537338,Human_Splice_Rec_537339,Human_Splice_Rec_537360,Human_Splice_Rec_537361,Human_Splice_Rec_537378,Human_Splice_Rec_537379,Human_Splice_Rec_537400,Human_Splice_Rec_537401,Human_Splice_Rec_537408,Human_Splice_Rec_537409,Human_Splice_Rec_537414,Human_Splice_Rec_537415,Human_Splice_Rec_537418,Human_Splice_Rec_537419,Human_Splice_Rec_537424 Human_miRNA_ID_273480,Human_miRNA_ID_2050806,Human_miRNA_ID_2238288 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238 111133 RMVar_ID_111133 Human_SNP_ID_854676481 m1A Human chr4 + 18021722 18021701 18021722 GCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GCGGCGGCGGCG_____________________GCGGCCATTCTCTCTCTTCCCTTGTCCATCTG GGCGGCAGCAGCGGCGGCGGCA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:18021620..18021727 26863196 MeRIP-seq:(Medium) rs777073080 Functional Loss DEL ICGC 13..33 33 KICH 1 - 111134 RMVar_ID_111134 Human_SNP_ID_854681951 m1A Human chr4 + 1025622 1025622 1025622 CGCACATGCACAGATATGCCGCCTGGGCACACAGATAAGCTGCCCAAATGCACGCACACGCACAG CGCACATGCACAGATATGCCGCCTGGGCACACTGATAAGCTGCCCAAATGCACGCACACGCACAG A T FGFRL1 Ensembl:ENSG00000127418 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1025571..1025700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_213246,Human_RBP_ID_610159,Human_RBP_ID_17409397 Human_miRNA_ID_323931,Human_miRNA_ID_2204964,Human_miRNA_ID_2928697 RMVar_hsa_circ_97374,RMVar_hsa_circ_115423,RMVar_hsa_circ_75612,RMVar_hsa_circ_224221,RMVar_hsa_circ_224222,RMVar_hsa_circ_95312,RMVar_hsa_circ_224223,RMVar_hsa_circ_224224 111135 RMVar_ID_111135 Human_SNP_ID_854686726 m1A Human chr4 - 168877830 168877830 168877830 CCGCGAGCTCGGGGAAGGCGGGCGGCGGCGGGAAGGGGGGCGAGGGCGGCGCGCTGCGCGGGGCT CCGCGAGCTCGGGGAAGGCGGGCGGCGGCGGGGAGGGGGGCGAGGGCGGCGCGCTGCGCGGGGCT T C CBR4 Ensembl:ENSG00000145439 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:168877779..168878025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_229479 111136 RMVar_ID_111136 Human_SNP_ID_854721413 m1A Human chr4 + 8228023 8228023 8228023 CCCACTACCTCAGGCAAGCGCTGGCCTCCCTGACCCCGGGCACAGGCCAGGCGCTGCGCGGCCCC CCCACTACCTCAGGCAAGCGCTGGCCTCCCTGTCCCCGGGCACAGGCCAGGCGCTGCGCGGCCCC A T SH3TC1 Ensembl:ENSG00000125089 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:8227894..8228073 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_22096242 RMVar_hsa_circ_80135,RMVar_hsa_circ_104979,RMVar_hsa_circ_224785,RMVar_hsa_circ_88219,RMVar_hsa_circ_105322,RMVar_hsa_circ_224786,RMVar_hsa_circ_224787,RMVar_hsa_circ_224789,RMVar_hsa_circ_77571,RMVar_hsa_circ_224790 111137 RMVar_ID_111137 Human_SNP_ID_854754571 m1A Human chr4 - 7042790 7042790 7042790 ACCCGGGGAGCTGGAGTCGGAGCCGGAGGAGGAGGAGGAGGAGCAAGCGGCTTCGCAGGGAGGCA ACCCGGGGAGCTGGAGTCGGAGCCGGAGGAGGTGGAGGAGGAGCAAGCGGCTTCGCAGGGAGGCA T A AC097382.2,CCDC96 Ensembl:ENSG00000245748,Ensembl:ENSG00000173013 lincRNA,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7042288..7042915 26863196 MeRIP-seq:(Medium) rs1222988578 Functional Loss SNV ICGC 33..33 33 THCA 1 - 111138 RMVar_ID_111138 Human_SNP_ID_854764260 m1A Human chr4 - 2409302 2409302 2409302 GCTGGGACTGGTGGGTGGCGGGGATTCCAGCGAGAGGATGGCAGCAGGCGACTCTGGATGGAGAA GCTGGGACTGGTGGGTGGCGGGGATTCCAGCGGGAGGATGGCAGCAGGCGACTCTGGATGGAGAA T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:2409200..2409435;chr4:2409057..2409587;chr4:2409071..2409547 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 111139 RMVar_ID_111139 Human_SNP_ID_854988364 m1A Human chr4 - 73258319 73258319 73258319 TGGCGGCGGCGGCACCAGCAGTAACAACAGCGAGGAAGAAGAGGACGACGACGACGAGGAAGAGG TGGCGGCGGCGGCACCAGCAGTAACAACAGCGGGGAAGAAGAGGACGACGACGACGAGGAAGAGG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:73258276..73258450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_71358,Human_RBP_ID_248983,Human_RBP_ID_838045,Human_RBP_ID_2856240,Human_RBP_ID_9396394,Human_RBP_ID_23034914,Human_RBP_ID_26349363,Human_RBP_ID_27824200 Human_Splice_Rec_568559 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_94797,RMVar_hsa_circ_226578 111140 RMVar_ID_111140 Human_SNP_ID_855024763 m1A Human chr4 + 8227970 8227970 8227970 GAACCTGGTGCTCCAGAACGCCCCCCAGCCCCACAGCCTCCCTGCCCAAACTTCCCACTACCTCA GAACCTGGTGCTCCAGAACGCCCCCCAGCCCCCCAGCCTCCCTGCCCAAACTTCCCACTACCTCA A C SH3TC1 Ensembl:ENSG00000125089 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:8227919..8228018 26863196 MeRIP-seq:(Medium) rs780192982 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_27509572 Human_miRNA_ID_1036887,Human_miRNA_ID_1371338,Human_miRNA_ID_2028528,Human_miRNA_ID_2689068,Human_miRNA_ID_2692251,Human_miRNA_ID_2713077,Human_miRNA_ID_3049055 RMVar_hsa_circ_80135,RMVar_hsa_circ_104979,RMVar_hsa_circ_224785,RMVar_hsa_circ_88219,RMVar_hsa_circ_105322,RMVar_hsa_circ_224786,RMVar_hsa_circ_224787,RMVar_hsa_circ_224789,RMVar_hsa_circ_77571,RMVar_hsa_circ_224790 111141 RMVar_ID_111141 Human_SNP_ID_855038772 m1A Human chr4 + 1723846 1723846 1723846 TCAGGATGACACCCTTGGACTGGAAAACTCACACCCGGTCTGGACACAGAAAGAGAAGTAAGTGT TCAGGATGACACCCTTGGACTGGAAAACTCACGCCCGGTCTGGACACAGAAAGAGAAGTAAGTGT A G TACC3 Ensembl:ENSG00000013810 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1723798..1723905 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1636327,Human_RBP_ID_5448464,Human_RBP_ID_8878126,Human_RBP_ID_9304267,Human_RBP_ID_9396906,Human_RBP_ID_15094638,Human_RBP_ID_17294076,Human_RBP_ID_17407592,Human_RBP_ID_18021911,Human_RBP_ID_22095342,Human_RBP_ID_27507131 Human_Splice_Rec_537657,Human_Splice_Rec_537663,Human_Splice_Rec_537693,Human_Splice_Rec_537723,Human_Splice_Rec_537735,Human_Splice_Rec_537753,Human_Splice_Rec_537783,Human_Splice_Rec_537815,Human_Splice_Rec_537821,Human_Splice_Rec_537851 RMVar_hsa_circ_368001,RMVar_hsa_circ_370336,RMVar_hsa_circ_115555,RMVar_hsa_circ_105378,RMVar_hsa_circ_224257,RMVar_hsa_circ_224258,RMVar_hsa_circ_224256,RMVar_hsa_circ_224259 111142 RMVar_ID_111142 Human_SNP_ID_855096455 m1A Human chr4 + 65573519 65573519 65573519 ATACTAAAGAGAAGAAACCCGAAGCCAAGAAGACTGATGCTGGTGGCAAGGTGAAAAAGGGTAAC ATACTAAAGAGAAGAAACCCGAAGCCAAGAAGGCTGATGCTGGTGGCAAGGTGAAAAAGGGTAAC A G AC115223.1 Ensembl:ENSG00000243199 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_miRNA_ID_1855996,Human_miRNA_ID_1858985 111143 RMVar_ID_111143 Human_SNP_ID_855122130 m1A Human chr4 + 56451987 56451987 56451987 GAAGGCCTGTGGAAATTTTGGCATTCCATGTGAACTTCGAGTAACATCTGCGCATAAAGGACCAG GAAGGCCTGTGGAAATTTTGGCATTCCATGTGGACTTCGAGTAACATCTGCGCATAAAGGACCAG A G PAICS Ensembl:ENSG00000128050 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 4 kidney Human_RBP_ID_622468,Human_RBP_ID_941642,Human_RBP_ID_1036848,Human_RBP_ID_1639497,Human_RBP_ID_1979898,Human_RBP_ID_7319595,Human_RBP_ID_8880408,Human_RBP_ID_9161520,Human_RBP_ID_15178650,Human_RBP_ID_18032114,Human_RBP_ID_22094664,Human_RBP_ID_22458603,Human_RBP_ID_23034802,Human_RBP_ID_23213989,Human_RBP_ID_24059642,Human_RBP_ID_27068797,Human_RBP_ID_27729047 Human_Splice_Rec_563305,Human_Splice_Rec_563323,Human_Splice_Rec_563341,Human_Splice_Rec_563363,Human_Splice_Rec_563379 RMVar_hsa_circ_336530,RMVar_hsa_circ_85946,RMVar_hsa_circ_110670,RMVar_hsa_circ_226228,RMVar_hsa_circ_372952,RMVar_hsa_circ_88685,RMVar_hsa_circ_226227,RMVar_hsa_circ_88998,RMVar_hsa_circ_226229,RMVar_hsa_circ_226230,RMVar_hsa_circ_226231,RMVar_hsa_circ_226232,RMVar_hsa_circ_314821 111144 RMVar_ID_111144 Human_SNP_ID_855131193 m1A Human chr4 - 6693943 6693943 6693943 AGACGTCTATGATCATGCCCATGGCTGTCTCTAGTTCCGTCATGGTGCTAGATTCAGACCCACCT AGACGTCTATGATCATGCCCATGGCTGTCTCTCGTTCCGTCATGGTGCTAGATTCAGACCCACCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6693851..6694234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 meninges anaplastic 1 brain 111145 RMVar_ID_111145 Human_SNP_ID_855152279 m1A Human chr4 + 6709341 6709341 6709341 AATCTCCTTGGCTTTCTCCTCAGCCTTCTCGCACAACTCCGACACTCTCTCGTCGGCTTCGCCAC AATCTCCTTGGCTTTCTCCTCAGCCTTCTCGCGCAACTCCGACACTCTCTCGTCGGCTTCGCCAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr4:6709226..6709820;chr4:6709226..6709875 26863196 MeRIP-seq:(Medium) rs759990042 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111146 RMVar_ID_111146 Human_SNP_ID_855197844 m1A Human chr4 - 82423591 82423591 82423591 TACGTGTTCACAGGCAGAGTAGTTGATCTCACACAACGGGTGATCTCACAAAACTGGTAAGTTTC TACGTGTTCACAGGCAGAGTAGTTGATCTCACGCAACGGGTGATCTCACAAAACTGGTAAGTTTC T C HNRNPDL Ensembl:ENSG00000152795 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9316 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_7332076,Human_RBP_ID_15245379,Human_RBP_ID_17296314,Human_RBP_ID_18032409 Human_miRNA_ID_323881 GWAS_ID_8923,GWAS_ID_8924 111147 RMVar_ID_111147 Human_SNP_ID_855233139 m1A Human chr4 + 49635526 49635526 49635526 TGAATGGAATGGAATCAACACGAGTGGAAAGGAATGGAATGGAATGGAATGGAATGGAATGGAAT TGAATGGAATGGAATCAACACGAGTGGAAAGGCATGGAATGGAATGGAATGGAATGGAATGGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49635476..49635584 26863196 MeRIP-seq:(Medium) rs796542969 Functional Loss SNV ICGC 33..33 33 COCA 1 - 111148 RMVar_ID_111148 Human_SNP_ID_855241498 m1A Human chr4 - 57109937 57109937 57109937 CGAGCGGCTGCCAGCTGCGCGCCGCCAGCCAGAGGGCCGAGAGCCGCGGGGAGAAGGCCATCACC CGAGCGGCTGCCAGCTGCGCGCCGCCAGCCAGTGGGCCGAGAGCCGCGGGGAGAAGGCCATCACC T A IGFBP7 Ensembl:ENSG00000163453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:57109811..57179184 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_563965,Human_Splice_Rec_563973 RMVar_hsa_circ_265476 111149 RMVar_ID_111149 Human_SNP_ID_855272471 m1A Human chr4 + 18021710 18021698 18021710 CGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC CGGCACTGAGCGGCGGCGGCG____________GCGGCGGCGGCAGCGGCCATTCTCTCTCTTCC GGCGGCGGCAGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr4:18021615..18021731;chr4:18021612..18021849 26863196 MeRIP-seq:(Medium) rs769142181 Functional Loss DEL ICGC 22..33 33 ESCA 1 - 111150 RMVar_ID_111150 Human_SNP_ID_855277301 m1A Human chr4 - 48906719 48906719 48906719 GCTGGAGCGGGCCGGCGGTGCAGTCACGGGGGAGCGAGGCCTGCTGGGCTTGGCAACGAGGGACT GCTGGAGCGGGCCGGCGGTGCAGTCACGGGGGGGCGAGGCCTGCTGGGCTTGGCAACGAGGGACT T C OCIAD2 Ensembl:ENSG00000145247 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:48904576..48906788 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 3 - Human_Splice_Rec_560375,Human_Splice_Rec_560387,Human_Splice_Rec_560397,Human_Splice_Rec_560407,Human_Splice_Rec_560417,Human_Splice_Rec_560427,Human_Splice_Rec_560433,Human_Splice_Rec_560447 111151 RMVar_ID_111151 Human_SNP_ID_855305072 m1A Human chr4 - 140154130 140154130 140154130 GGAGGAGGTGGAGGAGCGAGAGGAGGAGGAGGAGGCGGCGGCGGCGGCGGCGGCGAGCAGTTGAT GGAGGAGGTGGAGGAGCGAGAGGAGGAGGAGGCGGCGGCGGCGGCGGCGGCGGCGAGCAGTTGAT T G MAML3 Ensembl:ENSG00000196782 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:140154004..140154217 26863196 MeRIP-seq:(Medium) rs868585487 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,STAD 3 lung 111152 RMVar_ID_111152 Human_SNP_ID_855344638 m1A Human chr4 - 128287474 128287474 128287474 GCCTCGCATGAAGAAGCGGGACTTCAGCTTGGAGCAGCTGCGCCAGTACGACGGCTCCCGCAACC GCCTCGCATGAAGAAGCGGGACTTCAGCTTGGCGCAGCTGCGCCAGTACGACGGCTCCCGCAACC T G PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:128287351..128287500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_613268,Human_RBP_ID_1634972,Human_RBP_ID_5121264,Human_RBP_ID_5150866,Human_RBP_ID_7267208,Human_RBP_ID_9335073,Human_RBP_ID_9354509,Human_RBP_ID_15044553,Human_RBP_ID_22510227,Human_RBP_ID_27062393 111153 RMVar_ID_111153 Human_SNP_ID_855373528 m1A Human chr4 - 70688651 70688651 70688651 CACCATGGCTCACAATCTCAGGTTTTACAGCGACTCCGGACTTTCGGCCACCACTGACTTCGGCG CACCATGGCTCACAATCTCAGGTTTTACAGCGGCTCCGGACTTTCGGCCACCACTGACTTCGGCG T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr4:70688558..70688713 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111154 RMVar_ID_111154 Human_SNP_ID_855383848 m1A Human chr4 + 3316290 3316290 3316290 GCCGGCTACGGATTCACGCTTTCGGGACAGGCACCCTGTGTGCTCAGCTGCGTCATGAGAGGGAG GCCGGCTACGGATTCACGCTTTCGGGACAGGCGCCCTGTGTGCTCAGCTGCGTCATGAGAGGGAG A G RGS12 Ensembl:ENSG00000159788 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:3316141..3316292 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_942197,Human_RBP_ID_5531180,Human_RBP_ID_19013591 Human_miRNA_ID_2224981 RMVar_hsa_circ_285099,RMVar_hsa_circ_224551,RMVar_hsa_circ_377810,RMVar_hsa_circ_314583,RMVar_hsa_circ_224553,RMVar_hsa_circ_273907,RMVar_hsa_circ_224552 111155 RMVar_ID_111155 Human_SNP_ID_855429683 m1A Human chr4 - 41360938 41360938 41360938 AGTGCAAGGCCGCCCGCCAGCCACCCGCACCTACCTCAATCCACTTCTGCGCCTCGGAGAAGGCG AGTGCAAGGCCGCCCGCCAGCCACCCGCACCTGCCTCAATCCACTTCTGCGCCTCGGAGAAGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:41360770..41360981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111156 RMVar_ID_111156 Human_SNP_ID_855466209 m1A Human chr4 - 11372839 11372839 11372839 GGAGCGGCTCCTGTGGCGGCGGCGGCCCGGGGACCGTGATCTCCGGCGCACGGGGGACCTGCGCC GGAGCGGCTCCTGTGGCGGCGGCGGCCCGGGGGCCGTGATCTCCGGCGCACGGGGGACCTGCGCC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr4:11372746..11372892 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111157 RMVar_ID_111157 Human_SNP_ID_855478228 m1A Human chr4 - 673374 673374 673374 AACAGATTACCTAAAACCTCGGGCAGAAGAGGAGAGGAGGATAGCAGCAGAAGAGAAGAAGAAGC AACAGATTACCTAAAACCTCGGGCAGAAGAGGGGAGGAGGATAGCAGCAGAAGAGAAGAAGAAGC T C ATP5ME Ensembl:ENSG00000169020 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:673273..673466;chr4:672426..673466 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_786280,Human_RBP_ID_837951,Human_RBP_ID_7321361,Human_RBP_ID_9395973,Human_RBP_ID_17662039,Human_RBP_ID_17671439,Human_RBP_ID_19121285,Human_RBP_ID_22458535,Human_RBP_ID_24072666,Human_RBP_ID_24547758,Human_RBP_ID_26348858,Human_RBP_ID_27823907 Human_Splice_Rec_535520,Human_Splice_Rec_535521,Human_Splice_Rec_535526,Human_Splice_Rec_535527,Human_Splice_Rec_535530,Human_Splice_Rec_535531,Human_Splice_Rec_535534,Human_Splice_Rec_535535,Human_Splice_Rec_535537 RMVar_hsa_circ_83130,RMVar_hsa_circ_103935,RMVar_hsa_circ_224182,RMVar_hsa_circ_224183 111158 RMVar_ID_111158 Human_SNP_ID_855566502 m1A Human chr4 - 48710695 48710695 48710695 ACCATATTTCCTATTTTTTAATCTTCCAGCCTAGAACATTCCATATTCTGCTTCACACACGGTGA ACCATATTTCCTATTTTTTAATCTTCCAGCCTTGAACATTCCATATTCTGCTTCACACACGGTGA T A FRYL Ensembl:ENSG00000075539 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:48710604..48727437 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_559406,Human_Splice_Rec_559596,Human_Splice_Rec_559884,Human_Splice_Rec_560040,Human_Splice_Rec_560058 Human_miRNA_ID_1933080,Human_miRNA_ID_2196887,Human_miRNA_ID_2935892 RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_84281,RMVar_hsa_circ_225958,RMVar_hsa_circ_93802,RMVar_hsa_circ_225962,RMVar_hsa_circ_24962,RMVar_hsa_circ_2546,RMVar_hsa_circ_225970,RMVar_hsa_circ_225971,RMVar_hsa_circ_276310,RMVar_hsa_circ_358340,RMVar_hsa_circ_100943,RMVar_hsa_circ_225979,RMVar_hsa_circ_225977,RMVar_hsa_circ_225978,RMVar_hsa_circ_225976,RMVar_hsa_circ_103285,RMVar_hsa_circ_337869,RMVar_hsa_circ_297780,RMVar_hsa_circ_225980 111159 RMVar_ID_111159 Human_SNP_ID_855582069 m1A Human chr4 - 170072300 170072299 170072301 AAGACCCCAACTCTAAATATATATATATATATACACACACACATATATATACACACACACACATA AAGACCCCAACTCTAAATATATATATATATA__CACACACACATATATATACACACACACACATA GTA G AADAT Ensembl:ENSG00000109576 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr4:170072293..170072375 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 PBCA 1 - RMVar_hsa_circ_1471,RMVar_hsa_circ_63563,RMVar_hsa_circ_62645,RMVar_hsa_circ_229554,RMVar_hsa_circ_81680,RMVar_hsa_circ_34080 111160 RMVar_ID_111160 Human_SNP_ID_855595241 m1A Human chr4 - 151760947 151760947 151760947 GCGGCGCCCATGCTGCGCTGGGGCTGCCGTGGAAGACGTTGGGCTTTCGCCCGGGTTGACGGTGG GCGGCGCCCATGCTGCGCTGGGGCTGCCGTGGGAGACGTTGGGCTTTCGCCCGGGTTGACGGTGG T C GATB Ensembl:ENSG00000059691 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:151760777..151760959 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary Human_RBP_ID_786864,Human_RBP_ID_4795669,Human_RBP_ID_9396741 111161 RMVar_ID_111161 Human_SNP_ID_855620925 m1A Human chr4 - 141105435 141105435 141105435 AAAACAAGTTAAATTATGGAAACCTAGGAATGAGAGAATTTCAGTAAAGATGTATATTACAGTGC AAAACAAGTTAAATTATGGAAACCTAGGAATGGGAGAATTTCAGTAAAGATGTATATTACAGTGC T C RNF150 Ensembl:ENSG00000170153 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:141105428..141105690 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_15060449 RMVar_hsa_circ_228759 111162 RMVar_ID_111162 Human_SNP_ID_855622612 m1A Human chr4 - 6696879 6696877 6696879 CATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CATCCTTGTCTTTTCCACTCTAGAGGAGAGAG__GCTCAAGGTCAGCAGTGAGGGTGCCTGTGCA CCT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:6696876..6696925 26863196 MeRIP-seq:(Medium) rs753257885 Functional Loss DEL ICGC 33..34 33 STAD 1 - 111163 RMVar_ID_111163 Human_SNP_ID_855645344 m1A Human chr4 - 1849197 1849197 1849197 TTCCCCTGTTCCTGTTACAGGTAGTCCAGGGGATCCTGCTCATCTCAGCTGTGCCAGCACCCTGG TTCCCCTGTTCCTGTTACAGGTAGTCCAGGGGGTCCTGCTCATCTCAGCTGTGCCAGCACCCTGG T C LETM1 Ensembl:ENSG00000168924 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1849188..1856047 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_939877,Human_RBP_ID_4795257,Human_RBP_ID_5395082,Human_RBP_ID_22457795 Human_Splice_Rec_538212,Human_Splice_Rec_538213,Human_Splice_Rec_538252,Human_Splice_Rec_538253,Human_Splice_Rec_538264,Human_Splice_Rec_538265 Human_miRNA_ID_2064610,Human_miRNA_ID_2702485,Human_miRNA_ID_2933790 RMVar_hsa_circ_111913,RMVar_hsa_circ_224284,RMVar_hsa_circ_51890,RMVar_hsa_circ_344040 111164 RMVar_ID_111164 Human_SNP_ID_855681019 m1A Human chr4 - 2747913 2747913 2747913 GAAATTGAGAGGCTGACTGAGCGACTAGAAGAAAAAGAGAGGGAGATGCAGCAGCTGCTGAGCCA GAAATTGAGAGGCTGACTGAGCGACTAGAAGAGAAAGAGAGGGAGATGCAGCAGCTGCTGAGCCA T C TNIP2 Ensembl:ENSG00000168884 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:2747782..2747989 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_3737782,Human_RBP_ID_4783238,Human_RBP_ID_18447508 Human_Splice_Rec_539980,Human_Splice_Rec_539990,Human_Splice_Rec_540000,Human_Splice_Rec_540018,Human_Splice_Rec_540022 Human_miRNA_ID_2955229 RMVar_hsa_circ_347174,RMVar_hsa_circ_224391,RMVar_hsa_circ_85395 111165 RMVar_ID_111165 Human_SNP_ID_855730543 m1A Human chr4 - 170026087 170026087 170026087 GGCTGAGACTGCGGCGGAGGCTGCGCTGCGAGACGCCGCAGGGTCCGGGCAGCGGGCTCCAGGGG GGCTGAGACTGCGGCGGAGGCTGCGCTGCGAGCCGCCGCAGGGTCCGGGCAGCGGGCTCCAGGGG T G MFAP3L Ensembl:ENSG00000198948 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:170026070..170026363 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 111166 RMVar_ID_111166 Human_SNP_ID_855734243 m1A Human chr4 - 173333165 173333165 173333165 GAAGTCGAAGTTTGAAGATATGGCAAAAAGTGACAAAGCTCGCTATGACAGGGAGATGAAAAATT GAAGTCGAAGTTTGAAGATATGGCAAAAAGTGGCAAAGCTCGCTATGACAGGGAGATGAAAAATT T C HMGB2 Ensembl:ENSG00000164104 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_283217,Human_RBP_ID_941099,Human_RBP_ID_1636481,Human_RBP_ID_1974764,Human_RBP_ID_4777966,Human_RBP_ID_7287824,Human_RBP_ID_8587299,Human_RBP_ID_8878207,Human_RBP_ID_9152993,Human_RBP_ID_9396791,Human_RBP_ID_15096379,Human_RBP_ID_17294130,Human_RBP_ID_18032232,Human_RBP_ID_18447357,Human_RBP_ID_24045099,Human_RBP_ID_25829920,Human_RBP_ID_26348936,Human_RBP_ID_27825180 Human_Splice_Rec_623120,Human_Splice_Rec_623121,Human_Splice_Rec_623126,Human_Splice_Rec_623127,Human_Splice_Rec_623134,Human_Splice_Rec_623135,Human_Splice_Rec_623140,Human_Splice_Rec_623144,Human_Splice_Rec_623145 Human_miRNA_ID_2443625 RMVar_hsa_circ_44926,RMVar_hsa_circ_94472,RMVar_hsa_circ_229577 111167 RMVar_ID_111167 Human_SNP_ID_855746653 m1A Human chr4 + 82358819 82358819 82358819 TCCCATTCAATTTATGTTCTTTTTGATCCATGACCTAAGGAAATTGAAGTTTTCATTTAAAAAAT TCCCATTCAATTTATGTTCTTTTTGATCCATGGCCTAAGGAAATTGAAGTTTTCATTTAAAAAAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:82358776..82358825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111168 RMVar_ID_111168 Human_SNP_ID_855767165 m1A Human chr4 - 8619564 8619564 8619564 TGGCCTGTGGGTGCTCAGCGATGTGAAGTAGGACCACCACCAGGGCTTACTCCCGTCGGCCGAGG TGGCCTGTGGGTGCTCAGCGATGTGAAGTAGGGCCACCACCAGGGCTTACTCCCGTCGGCCGAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:8619408..8619711 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_15217507 111169 RMVar_ID_111169 Human_SNP_ID_855790372 m1A Human chr4 - 120060974 120060974 120060974 AATTAATTGATTTGATTTTTTTTTGACAGTGCACCCAGAGAAAAGTCTCAGAAAGCTATCCAGGA AATTAATTGATTTGATTTTTTTTTGACAGTGCGCCCAGAGAAAAGTCTCAGAAAGCTATCCAGGA T C MAD2L1 Ensembl:ENSG00000164109 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs778506790 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_939765,Human_RBP_ID_22458711 Human_Splice_Rec_602272,Human_Splice_Rec_602278,Human_Splice_Rec_602284 RMVar_hsa_circ_95520,RMVar_hsa_circ_228319 111170 RMVar_ID_111170 Human_SNP_ID_855811719 m1A Human chr4 - 2933896 2933896 2933896 CCACCATGGGATGGGGAGGGGGTGGAGGCTGCACCCCGCGCCCACCCATCCACCAGCAGCCGCCG CCACCATGGGATGGGGAGGGGGTGGAGGCTGCGCCCCGCGCCCACCCATCCACCAGCAGCCGCCG T C MFSD10 Ensembl:ENSG00000109736 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:2933776..2934442 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_4794544,Human_RBP_ID_8130405,Human_RBP_ID_8212530,Human_RBP_ID_9334614,Human_RBP_ID_9435965,Human_RBP_ID_22457799 Human_Splice_Rec_540748,Human_Splice_Rec_540794,Human_Splice_Rec_540818,Human_Splice_Rec_540858,Human_Splice_Rec_540890 RMVar_hsa_circ_7810 111171 RMVar_ID_111171 Human_SNP_ID_855824371 m1A Human chr4 - 3953151 3953151 3953151 CTCCACACAGAGCTTAGAAGCAAAGTTAAGAGACTCATCAGATTCTGAGCTGCGGCGGGATATTT CTCCACACAGAGCTTAGAAGCAAAGTTAAGAGGCTCATCAGATTCTGAGCTGCGGCGGGATATTT T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs58515458 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5607578 Human_Splice_Rec_542142,Human_Splice_Rec_542143,Human_Splice_Rec_542172,Human_Splice_Rec_542173,Human_Splice_Rec_542180,Human_Splice_Rec_542181,Human_Splice_Rec_542188,Human_Splice_Rec_542189,Human_Splice_Rec_542192,Human_Splice_Rec_542193,Human_Splice_Rec_542198,Human_Splice_Rec_542199,Human_Splice_Rec_542211,Human_Splice_Rec_542215,Human_Splice_Rec_542222,Human_Splice_Rec_542223,Human_Splice_Rec_542230,Human_Splice_Rec_542231 111172 RMVar_ID_111172 Human_SNP_ID_855857093 m1A Human chr4 - 164196971 164196971 164196971 CCTGAAGATGAGGGAGAAGATGATGACTAAGTAGAATAACCTATTTTGAAAAATTCCTATTGTGA CCTGAAGATGAGGGAGAAGATGATGACTAAGTGGAATAACCTATTTTGAAAAATTCCTATTGTGA T C MARCHF1 Ensembl:ENSG00000145416 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1484609627 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_17408 111173 RMVar_ID_111173 Human_SNP_ID_855883622 m1A Human chr4 + 112232135 112232135 112232135 CTGCTGGACGCAGTGCTTCGGACTGCTTCGCAAGGAAGCGGGGCGGCTGCAGCGAGTAGGCGGCG CTGCTGGACGCAGTGCTTCGGACTGCTTCGCAGGGAAGCGGGGCGGCTGCAGCGAGTAGGCGGCG A G AP1AR Ensembl:ENSG00000138660 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:112232085..112253269 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney Human_RBP_ID_611666,Human_RBP_ID_4795597,Human_RBP_ID_23120141 Human_Splice_Rec_592877,Human_Splice_Rec_592889,Human_Splice_Rec_592907,Human_Splice_Rec_592911,Human_Splice_Rec_592927 111174 RMVar_ID_111174 Human_SNP_ID_855927303 m1A Human chr4 - 25377340 25377340 25377340 CCACGAGGAGCCCCGACCGCGCCTGTACCTGCAAGAGTCCCCACCGGCAGACTAACACGGCCCCA CCACGAGGAGCCCCGACCGCGCCTGTACCTGCTAGAGTCCCCACCGGCAGACTAACACGGCCCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:25377235..25377418 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 111175 RMVar_ID_111175 Human_SNP_ID_855940525 m1A Human chr4 + 56314527 56314527 56314527 GAGGCGGCGGCTGGAGGAGGACGCCAGGCTGGAGGAGCGGAGGCGGCAGGAGGAGGAGGAAGGAA GAGGCGGCGGCTGGAGGAGGACGCCAGGCTGGGGGAGCGGAGGCGGCAGGAGGAGGAGGAAGGAA A G CRACD Ensembl:ENSG00000109265 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:56314399..56314820 26863196 MeRIP-seq:(Medium) rs1305564060 Functional Loss SNV ICGC 33..33 33 THCA 1 - RMVar_hsa_circ_302627,RMVar_hsa_circ_266430,RMVar_hsa_circ_30363,RMVar_hsa_circ_226214 111176 RMVar_ID_111176 Human_SNP_ID_855971319 m1A Human chr4 - 140657800 140657800 140657800 TGTATACATCGCTGCCACAGGTGCACTGGTGGACCAAGGTGTCTTTGAGGAGCTAGCACGAGACT TGTATACATCGCTGCCACAGGTGCACTGGTGGGCCAAGGTGTCTTTGAGGAGCTAGCACGAGACT T C TBC1D9 Ensembl:ENSG00000109436 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr4:140657768..140658015 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_941030,Human_RBP_ID_8877574 Human_Splice_Rec_610130 RMVar_hsa_circ_80093,RMVar_hsa_circ_92618,RMVar_hsa_circ_122876,RMVar_hsa_circ_85492,RMVar_hsa_circ_228742,RMVar_hsa_circ_76160,RMVar_hsa_circ_228744,RMVar_hsa_circ_228743,RMVar_hsa_circ_228740,RMVar_hsa_circ_228741,RMVar_hsa_circ_23328,RMVar_hsa_circ_328600,RMVar_hsa_circ_12633,RMVar_hsa_circ_30178,RMVar_hsa_circ_346206,RMVar_hsa_circ_306597,RMVar_hsa_circ_228746,RMVar_hsa_circ_15747,RMVar_hsa_circ_228747 111177 RMVar_ID_111177 Human_SNP_ID_855997211 m1A Human chr4 + 78551760 78551760 78551760 GGGCAGGAGGAAGGGGTGCGGTCGCGATCCGGACCCGGAGCCAGCGCGGAGCACCTGCGCCCGCG GGGCAGGAGGAAGGGGTGCGGTCGCGATCCGGGCCCGGAGCCAGCGCGGAGCACCTGCGCCCGCG A G ANXA3 Ensembl:ENSG00000138772 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr4:78551562..78551887;chr4:78551596..78551974 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_4795011 Human_Splice_Rec_572407,Human_Splice_Rec_572429,Human_Splice_Rec_572435,Human_Splice_Rec_572461,Human_Splice_Rec_572469,Human_Splice_Rec_572493 111178 RMVar_ID_111178 Human_SNP_ID_855997448 m1A Human chr4 - 128272477 128272477 128272477 TATGGAATATTTGCTGGTAGGGATGCCTCCAGAGGACTGGCCACATTTTGCCTAGATAAAGATGC TATGGAATATTTGCTGGTAGGGATGCCTCCAGGGGACTGGCCACATTTTGCCTAGATAAAGATGC T C PGRMC2 Ensembl:ENSG00000164040 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:128272426..128272525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver Human_RBP_ID_72888,Human_RBP_ID_613263,Human_RBP_ID_786632,Human_RBP_ID_941015,Human_RBP_ID_1387506,Human_RBP_ID_1634967,Human_RBP_ID_1972673,Human_RBP_ID_4772833,Human_RBP_ID_5266717,Human_RBP_ID_7267056,Human_RBP_ID_15044093,Human_RBP_ID_18032482,Human_RBP_ID_18343822,Human_RBP_ID_18818319,Human_RBP_ID_22770803,Human_RBP_ID_24035021,Human_RBP_ID_27506211 Human_Splice_Rec_606562,Human_Splice_Rec_606566,Human_Splice_Rec_606570,Human_Splice_Rec_606576,Human_Splice_Rec_606580,Human_Splice_Rec_606584,Human_Splice_Rec_606590 111179 RMVar_ID_111179 Human_SNP_ID_856033231 m1A Human chr4 + 1251091 1251091 1251091 TTCCCCATCGTCACTCTCCATGGCCTCCGTCTACACACAGTGTTCGTCTGCACAGCTTGTCAGCG TTCCCCATCGTCACTCTCCATGGCCTCCGTCTGCACACAGTGTTCGTCTGCACAGCTTGTCAGCG A G CTBP1-DT Ensembl:ENSG00000196810 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:1251043..1251155 26863196 MeRIP-seq:(Medium) rs1564508 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_RBP_ID_4795966,Human_RBP_ID_5102948,Human_RBP_ID_8266138 Human_miRNA_ID_3153296,Human_miRNA_ID_3160651 GWAS_ID_9212,GWAS_ID_9213,GWAS_ID_9214,GWAS_ID_9215,GWAS_ID_9216,GWAS_ID_9217,GWAS_ID_9218,GWAS_ID_9219,GWAS_ID_9220,GWAS_ID_9221,GWAS_ID_9222,GWAS_ID_9223,GWAS_ID_9224,GWAS_ID_9225,GWAS_ID_9226,GWAS_ID_9227,GWAS_ID_9228,GWAS_ID_9229,GWAS_ID_9230 111180 RMVar_ID_111180 Human_SNP_ID_856037889 m1A Human chr4 + 146182967 146182967 146182967 AGCAAACCCCTAGTGACTTCTTAAAGCAAATCATCGGACGACCAGTTGTGGTAAAATTAAATTCT AGCAAACCCCTAGTGACTTCTTAAAGCAAATCGTCGGACGACCAGTTGTGGTAAAATTAAATTCT A G LSM6 Ensembl:ENSG00000164167 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr4:146182901..146182975;chr4:146182873..146183025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_614740,Human_RBP_ID_1035423,Human_RBP_ID_1387671,Human_RBP_ID_1635673,Human_RBP_ID_1973518,Human_RBP_ID_3729976,Human_RBP_ID_4775108,Human_RBP_ID_5475158,Human_RBP_ID_15066187,Human_RBP_ID_18819281 Human_Splice_Rec_613012,Human_Splice_Rec_613013,Human_Splice_Rec_613020,Human_Splice_Rec_613021,Human_Splice_Rec_613026,Human_Splice_Rec_613027,Human_Splice_Rec_613032,Human_Splice_Rec_613033,Human_Splice_Rec_613038,Human_Splice_Rec_613039,Human_Splice_Rec_613047 RMVar_hsa_circ_43647,RMVar_hsa_circ_64106 111181 RMVar_ID_111181 Human_SNP_ID_856110962 m1A Human chr4 - 82426622 82426622 82426622 AATCATTGTGCATTGTTTCAGGTCAGGGCCAAAACTGGAACCAAGGATTTAATAACTATTATGAT AATCATTGTGCATTGTTTCAGGTCAGGGCCAATACTGGAACCAAGGATTTAATAACTATTATGAT T A HNRNPDL Ensembl:ENSG00000152795 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:82426433..82426659 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_837788,Human_RBP_ID_1037459,Human_RBP_ID_1069314,Human_RBP_ID_1981532,Human_RBP_ID_7332152,Human_RBP_ID_9396492,Human_RBP_ID_15209392,Human_RBP_ID_18413549,Human_RBP_ID_18826959,Human_RBP_ID_19014492,Human_RBP_ID_26349427,Human_RBP_ID_27824251 Human_Splice_Rec_573930,Human_Splice_Rec_573944,Human_Splice_Rec_573970,Human_Splice_Rec_573982,Human_Splice_Rec_573996,Human_Splice_Rec_574012,Human_Splice_Rec_574030,Human_Splice_Rec_574048,Human_Splice_Rec_574058 Human_miRNA_ID_2489844,Human_miRNA_ID_2751929 RMVar_hsa_circ_286669,RMVar_hsa_circ_366678,RMVar_hsa_circ_5743,RMVar_hsa_circ_95870,RMVar_hsa_circ_226963,RMVar_hsa_circ_60593 111182 RMVar_ID_111182 Human_SNP_ID_856113943 m1A Human chr4 - 99950245 99950245 99950245 GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTAGGTGGTGGGATCTCACCGTGGGTCCGATTAGC GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTTGGTGGTGGGATCTCACCGTGGGTCCGATTAGC T A H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:99950201..99950275 26863196 MeRIP-seq:(Medium) rs1263536050 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_12154,Human_RBP_ID_249138,Human_RBP_ID_283004,Human_RBP_ID_610129,Human_RBP_ID_786238,Human_RBP_ID_837765,Human_RBP_ID_1034584,Human_RBP_ID_1387144,Human_RBP_ID_1633766,Human_RBP_ID_1971068,Human_RBP_ID_3724441,Human_RBP_ID_4795069,Human_RBP_ID_5475863,Human_RBP_ID_5507142,Human_RBP_ID_7250988,Human_RBP_ID_8581262,Human_RBP_ID_9147974,Human_RBP_ID_9334756,Human_RBP_ID_15009286,Human_RBP_ID_18816461,Human_RBP_ID_22095603,Human_RBP_ID_22457730,Human_RBP_ID_22510051,Human_RBP_ID_23213841,Human_RBP_ID_24027302,Human_RBP_ID_24499635 Human_Splice_Rec_586239,Human_Splice_Rec_586241,Human_Splice_Rec_586249,Human_Splice_Rec_586273 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 111183 RMVar_ID_111183 Human_SNP_ID_856113947 m1A Human chr4 - 99950245 99950245 99950245 GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTAGGTGGTGGGATCTCACCGTGGGTCCGATTAGC GCGCAGTTTGAATCGCGGTGCGACGAAGGAGTGGGTGGTGGGATCTCACCGTGGGTCCGATTAGC T C H2AZ1 Ensembl:ENSG00000164032 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr4:99950201..99950275 26863196 MeRIP-seq:(Medium) rs1263536050 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_12154,Human_RBP_ID_249138,Human_RBP_ID_283004,Human_RBP_ID_610129,Human_RBP_ID_786238,Human_RBP_ID_837765,Human_RBP_ID_1034584,Human_RBP_ID_1387144,Human_RBP_ID_1633766,Human_RBP_ID_1971068,Human_RBP_ID_3724441,Human_RBP_ID_4795069,Human_RBP_ID_5475863,Human_RBP_ID_5507142,Human_RBP_ID_7250988,Human_RBP_ID_8581262,Human_RBP_ID_9147974,Human_RBP_ID_9334756,Human_RBP_ID_15009286,Human_RBP_ID_18816461,Human_RBP_ID_22095603,Human_RBP_ID_22457730,Human_RBP_ID_22510051,Human_RBP_ID_23213841,Human_RBP_ID_24027302,Human_RBP_ID_24499635 Human_Splice_Rec_586239,Human_Splice_Rec_586241,Human_Splice_Rec_586249,Human_Splice_Rec_586273 RMVar_hsa_circ_84416,RMVar_hsa_circ_227656 111184 RMVar_ID_111184 Human_SNP_ID_856124620 m1A Human chr4 + 38944865 38944865 38944865 CCCGAGTCCGTGAAAAAATTGTCTTCCATGAAACCGGTCCCTGGTACCAGAAAGGTTGGGGACCA CCCGAGTCCGTGAAAAAATTGTCTTCCATGAAGCCGGTCCCTGGTACCAGAAAGGTTGGGGACCA A G FAM114A1 Ensembl:ENSG00000197712 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:38944844..38944944 32194978 MeRIP-seq:(Medium) rs1139089 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8212345 RMVar_hsa_circ_125537,RMVar_hsa_circ_225384 111185 RMVar_ID_111185 Human_SNP_ID_856125562 m1A Human chr4 - 53372 53372 53372 GGCTGAATCACCGAGGCCTCCCGGAGCCGAGAACGCAGAGAGCTGAAGCCCTAAACCAAGCCCTC GGCTGAATCACCGAGGCCTCCCGGAGCCGAGAGCGCAGAGAGCTGAAGCCCTAAACCAAGCCCTC T C lnc-ZNF732-9 RNACentral:URS00009BED6A lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:53334..53434 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111186 RMVar_ID_111186 Human_SNP_ID_856178544 m1A Human chr4 + 68314174 68314174 68314174 TCACATAATCGCTCTCTTTCTCTTTCTCTATCACGTCCTCTATCTCGCTCTCTGTCTCGTCTGTT TCACATAATCGCTCTCTTTCTCTTTCTCTATCGCGTCCTCTATCTCGCTCTCTGTCTCGTCTGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:68314124..68314284 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111187 RMVar_ID_111187 Human_SNP_ID_856195577 m1A Human chr4 - 173169112 173169112 173169112 GGCCAGGGAGGTCGGAGTGCGCGGGGCTCGGCACCCCCTCGGCCCGCGCTGCGCCAGCACCACCT GGCCAGGGAGGTCGGAGTGCGCGGGGCTCGGCCCCCCCTCGGCCCGCGCTGCGCCAGCACCACCT T G AC105285.1 Ensembl:ENSG00000245213 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:173169106..173169405 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111188 RMVar_ID_111188 Human_SNP_ID_856199533 m1A Human chr4 + 49098823 49098823 49098823 CCATTCCATTTCATTCCATTCCTTTCCATTCCATTCCACTCGGGTTGATTCCGTTGCATTCCATT CCATTCCATTTCATTCCATTCCTTTCCATTCCCTTCCACTCGGGTTGATTCCGTTGCATTCCATT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49098811..49098898 26863196 MeRIP-seq:(Medium) rs1057029391 Functional Loss SNV ICGC 33..33 33 LUSC 2 - 111189 RMVar_ID_111189 Human_SNP_ID_856226766 m1A Human chr4 - 947788 947788 947788 CCCAGCGTCCTCGTCTCTCCTGCCTGGGGGGCAGTCCCCCGGTGTATCCAGTGCCTGCTCTGGGG CCCAGCGTCCTCGTCTCTCCTGCCTGGGGGGCCGTCCCCCGGTGTATCCAGTGCCTGCTCTGGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:947742..947813 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 111190 RMVar_ID_111190 Human_SNP_ID_856233655 m1A Human chr4 - 75645520 75645520 75645520 GGTGGAATGATGCGTGATCGTGATGGAAGAGGACCTCCTCCAAGGGGTGGCATGGCACAGAAACT GGTGGAATGATGCGTGATCGTGATGGAAGAGGGCCTCCTCCAAGGGGTGGCATGGCACAGAAACT T C G3BP2 Ensembl:ENSG00000138757 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:75645469..75645675 26863196 MeRIP-seq:(Medium) rs1025359506 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_786481,Human_RBP_ID_1980927,Human_RBP_ID_5150639,Human_RBP_ID_7327476,Human_RBP_ID_8881041,Human_RBP_ID_9304178,Human_RBP_ID_9396401,Human_RBP_ID_15199635,Human_RBP_ID_22457696,Human_RBP_ID_24064268,Human_RBP_ID_26349367 111191 RMVar_ID_111191 Human_SNP_ID_856294709 m1A Human chr4 + 55546520 55546520 55546520 GCTTGCGGCGGCTCCGGCTTCTTCCCTCCCCCACCCAGGTCTCCCGCTGCGGTGACTCGGAACCA GCTTGCGGCGGCTCCGGCTTCTTCCCTCCCCCCCCCAGGTCTCCCGCTGCGGTGACTCGGAACCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:55546514..55546615 26863196 MeRIP-seq:(Medium) rs1022095596 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111192 RMVar_ID_111192 Human_SNP_ID_856354439 m1A Human chr4 + 150078524 150078524 150078524 GGATCCGGGCGCGGCCGAGGCGGCGGCGCTGCACCCCGGGCCTGGGCCCGCGCGACTCCCCCGGG GGATCCGGGCGCGGCCGAGGCGGCGGCGCTGCCCCCCGGGCCTGGGCCCGCGCGACTCCCCCGGG A C DCLK2 Ensembl:ENSG00000170390 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:150078478..150078551 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111193 RMVar_ID_111193 Human_SNP_ID_856365318 m1A Human chr4 + 74158208 74158208 74158208 GCCGCCTTGGCCGAGCGCCGGCGTTGGGCAGAAGCACAGCACCCTCCGTAAGGGCACCGGGAGAG GCCGCCTTGGCCGAGCGCCGGCGTTGGGCAGAGGCACAGCACCCTCCGTAAGGGCACCGGGAGAG A G MTHFD2L Ensembl:ENSG00000163738 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:74158161..74158310 26863196 MeRIP-seq:(Medium) rs1353574820 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 3 liver Human_RBP_ID_837654,Human_RBP_ID_4794994,Human_RBP_ID_19014459,Human_RBP_ID_23034700,Human_RBP_ID_24063768 Human_Splice_Rec_569285,Human_Splice_Rec_569297,Human_Splice_Rec_569311,Human_Splice_Rec_569313,Human_Splice_Rec_569327,Human_Splice_Rec_569341 Human_miRNA_ID_2236340 RMVar_hsa_circ_100789,RMVar_hsa_circ_226587 111194 RMVar_ID_111194 Human_SNP_ID_856365334 m1A Human chr4 + 3520126 3520126 3520126 CTGGGGTCATCCAGCCCGTCTTCCTGGGTGCCACTGAGGGAGTTGCTGGTCACCTGCCGAGCGTC CTGGGGTCATCCAGCCCGTCTTCCTGGGTGCCTCTGAGGGAGTTGCTGGTCACCTGCCGAGCGTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:3520036..3520229 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung 111195 RMVar_ID_111195 Human_SNP_ID_856377992 m1A Human chr4 + 107614384 107614384 107614384 ATTCGTGTTCCTGAAATAAATTCAAAGTCTTCATGGCTAAAGGAGAGGAAAAAAAGAAAATTATT ATTCGTGTTCCTGAAATAAATTCAAAGTCTTCGTGGCTAAAGGAGAGGAAAAAAAGAAAATTATT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:107614238..107631631 32194978 MeRIP-seq:(Medium) rs768649817 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111196 RMVar_ID_111196 Human_SNP_ID_856378216 m1A Human chr4 - 1046574 1046562 1046574 CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGGACTCGGGAATGGCTCGGGAAGGGCTCGGGAAGG CTGGGGAAAGGCTCGGGAAGGGCTCTGGAAGG____________CTCGGGAAGGGCTCGGGAAGG GCCATTCCCGAGT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:1046566..1046650 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..44 33 SKCA 1 - 111197 RMVar_ID_111197 Human_SNP_ID_856421874 m1A Human chr4 - 41655834 41655834 41655834 GAGGGAACAAAAGGAGAGGCAAAAAGAGCTGCAGGAAGGGCCAGGCATGGTGGCTCATGCCTATA GAGGGAACAAAAGGAGAGGCAAAAAGAGCTGCCGGAAGGGCCAGGCATGGTGGCTCATGCCTATA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr4:41655824..41655956 26863196 MeRIP-seq:(Medium) rs78977830 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_6639,GWAS_ID_6640,GWAS_ID_6641,GWAS_ID_6642,GWAS_ID_6643,GWAS_ID_6644,GWAS_ID_6645,GWAS_ID_6646,GWAS_ID_6647,GWAS_ID_6648,GWAS_ID_6649,GWAS_ID_6650,GWAS_ID_6651,GWAS_ID_6652,GWAS_ID_6653,GWAS_ID_6654,GWAS_ID_6655,GWAS_ID_6656,GWAS_ID_6657 111198 RMVar_ID_111198 Human_SNP_ID_856440371 m1A Human chr4 - 1025398 1025398 1025398 CCTTCGTCTGCAGCTCCGTCCTCCATCCTCCCAGTCTGCCTGTCTGGCCGGCCCCCCCGTGCCCA CCTTCGTCTGCAGCTCCGTCCTCCATCCTCCCGGTCTGCCTGTCTGGCCGGCCCCCCCGTGCCCA T C lnc-RNF212-3,lnc-RNF212-3:2,lnc-RNF212-3:3 RNACentral:URS00008C2DE4,RNACentral:URS00008C1F26,RNACentral:URS00009B8989 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:1025348..1025499 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111199 RMVar_ID_111199 Human_SNP_ID_856469633 m1A Human chr4 - 155375912 155375912 155375912 GCGAAGTCTGATTTGTTTTGTATATTTCAGCTACTATCAGAAGTTGAATTCTAATAATTAGCTAT GCGAAGTCTGATTTGTTTTGTATATTTCAGCTCCTATCAGAAGTTGAATTCTAATAATTAGCTAT T G MAP9 Ensembl:ENSG00000164114 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:155375874..155375967 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_Splice_Rec_617624,Human_Splice_Rec_617676,Human_Splice_Rec_617704,Human_Splice_Rec_617726,Human_Splice_Rec_617752,Human_Splice_Rec_617758 111200 RMVar_ID_111200 Human_SNP_ID_856502780 m1A Human chr4 + 18021707 18021707 18021707 CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT CTCCGGCACTGAGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCAGCGGCCATTCTCTCTCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:18021625..18021734 26863196 MeRIP-seq:(Medium) rs748344642 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COCA,ESCA,large_intestine adenocarcinoma 5 large intestine 111201 RMVar_ID_111201 Human_SNP_ID_856521916 m1A Human chr4 - 13601576 13601576 13601576 TAATGATGCACCACCAGGAACAAGTGCCAGCCAAGAAGGAGATGGTTCTGTGAATGATGGTACAG TAATGATGCACCACCAGGAACAAGTGCCAGCCCAGAAGGAGATGGTTCTGTGAATGATGGTACAG T G BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr4:13601527..13601634 32194978 MeRIP-seq:(Medium) rs61995954 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_91864,RMVar_hsa_circ_224876,RMVar_hsa_circ_101305,RMVar_hsa_circ_224880,RMVar_hsa_circ_265090 111202 RMVar_ID_111202 Human_SNP_ID_856533191 m1A Human chr4 - 3525001 3525001 3525001 AGGCTGGCCGAGCTCCACGCTGATCTGAAGATACAGGAGAGGGACGAACTCGCCTGGAAGAAACT AGGCTGGCCGAGCTCCACGCTGATCTGAAGATGCAGGAGAGGGACGAACTCGCCTGGAAGAAACT T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:3524951..3525000 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4799322,Human_RBP_ID_9396156,Human_RBP_ID_18823739,Human_RBP_ID_22457812,Human_RBP_ID_22770229,Human_RBP_ID_25808564,Human_RBP_ID_26349140 Human_Splice_Rec_542046,Human_Splice_Rec_542047,Human_Splice_Rec_542060,Human_Splice_Rec_542061,Human_Splice_Rec_542074,Human_Splice_Rec_542075,Human_Splice_Rec_542089,Human_Splice_Rec_542098,Human_Splice_Rec_542099,Human_Splice_Rec_542106,Human_Splice_Rec_542107 RMVar_hsa_circ_366215,RMVar_hsa_circ_41357 111203 RMVar_ID_111203 Human_SNP_ID_856543812 m1A Human chr4 + 49657632 49657632 49657632 GAATGAATCCGGGTGGAATGGAATGGAATGTAATGGAGTGGAATGGATTGGATTGGAGTGGAGTG GAATGAATCCGGGTGGAATGGAATGGAATGTATTGGAGTGGAATGGATTGGATTGGAGTGGAGTG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49657507..49657793 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111204 RMVar_ID_111204 Human_SNP_ID_856556476 m1A Human chr4 + 145180356 145180356 145180356 TTTCCTCCTCCGTACCGGTGTGAAGCGAGAAAACCCCCGCCCCTGGCGCGCACGCTGGGCCGGCT TTTCCTCCTCCGTACCGGTGTGAAGCGAGAAACCCCCCGCCCCTGGCGCGCACGCTGGGCCGGCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:145180310..145180532 26863196 MeRIP-seq:(Medium) rs977959034 Functional Loss SNV ICGC 33..33 33 SKCA 3 - 111205 RMVar_ID_111205 Human_SNP_ID_856562918 m1A Human chr4 - 1841799 1841799 1841799 TCTTACTACTGTTTTCCACTCTTCCCTTTTCAAGGAATGTTCCATTTGGCTGCTGCACTCCCATC TCTTACTACTGTTTTCCACTCTTCCCTTTTCACGGAATGTTCCATTTGGCTGCTGCACTCCCATC T G LETM1 Ensembl:ENSG00000168924 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr4:1841750..1843059 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_22678995 RMVar_hsa_circ_111913,RMVar_hsa_circ_224284,RMVar_hsa_circ_51890,RMVar_hsa_circ_344040 111206 RMVar_ID_111206 Human_SNP_ID_856579288 m1A Human chr4 - 75645526 75645526 75645526 GTGGGTGGTGGAATGATGCGTGATCGTGATGGAAGAGGACCTCCTCCAAGGGGTGGCATGGCACA GTGGGTGGTGGAATGATGCGTGATCGTGATGGGAGAGGACCTCCTCCAAGGGGTGGCATGGCACA T C G3BP2 Ensembl:ENSG00000138757 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr4:75645476..75645675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach Human_RBP_ID_786481,Human_RBP_ID_1980927,Human_RBP_ID_5150639,Human_RBP_ID_7327476,Human_RBP_ID_8881041,Human_RBP_ID_9304178,Human_RBP_ID_9396401,Human_RBP_ID_15199635,Human_RBP_ID_22457696,Human_RBP_ID_24064268,Human_RBP_ID_26349367 111207 RMVar_ID_111207 Human_SNP_ID_856607352 m1A Human chr4 + 165342967 165342967 165342967 AGCTTTATTTCTATTTACCCTTCCATTTTTGTATATCAAATTTCCATTGTCATTAAAAACTGTAT AGCTTTATTTCTATTTACCCTTCCATTTTTGTGTATCAAATTTCCATTGTCATTAAAAACTGTAT A G MSMO1 Ensembl:ENSG00000052802 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8733 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1641675,Human_RBP_ID_5475293,Human_RBP_ID_7285229,Human_RBP_ID_8212761,Human_RBP_ID_8950290,Human_RBP_ID_15237758,Human_RBP_ID_17296111,Human_RBP_ID_18345328,Human_RBP_ID_24431347,Human_RBP_ID_24500621,Human_RBP_ID_26518190,Human_RBP_ID_26691061 Human_miRNA_ID_756040,Human_miRNA_ID_1178568,Human_miRNA_ID_1632164,Human_miRNA_ID_1672663 RMVar_hsa_circ_100844,RMVar_hsa_circ_229435,RMVar_hsa_circ_110729,RMVar_hsa_circ_229437 111208 RMVar_ID_111208 Human_SNP_ID_856626975 m1A Human chr4 - 7789664 7789664 7789664 TGGATGGGGTGGTGAGGATAAAGAGGATGGAAAGCGGGCTGGTGCAGAGTGTGGGGAGATGCACG TGGATGGGGTGGTGAGGATAAAGAGGATGGAAGGCGGGCTGGTGCAGAGTGTGGGGAGATGCACG T C AFAP1 Ensembl:ENSG00000196526 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr4:7789334..7789822 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_5040,RMVar_hsa_circ_84246,RMVar_hsa_circ_105115,RMVar_hsa_circ_224743,RMVar_hsa_circ_82329,RMVar_hsa_circ_45455,RMVar_hsa_circ_224756,RMVar_hsa_circ_97678,RMVar_hsa_circ_31516,RMVar_hsa_circ_224746,RMVar_hsa_circ_224747,RMVar_hsa_circ_224748,RMVar_hsa_circ_101279,RMVar_hsa_circ_295472,RMVar_hsa_circ_371503,RMVar_hsa_circ_336675,RMVar_hsa_circ_116699,RMVar_hsa_circ_224749,RMVar_hsa_circ_224750,RMVar_hsa_circ_374508,RMVar_hsa_circ_224751,RMVar_hsa_circ_342172,RMVar_hsa_circ_332615,RMVar_hsa_circ_335664,RMVar_hsa_circ_318146,RMVar_hsa_circ_224752,RMVar_hsa_circ_224754,RMVar_hsa_circ_224755,RMVar_hsa_circ_224753 111209 RMVar_ID_111209 Human_SNP_ID_856629540 m1A Human chr4 + 49151034 49151034 49151034 TCCATTCCATTCCATTCCACTCGGGTTGATTCAATTCCGTTCCTTTCCATTCCATTCCATTCTAT TCCATTCCATTCCATTCCACTCGGGTTGATTCCATTCCGTTCCTTTCCATTCCATTCCATTCTAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49150870..49151040 26863196 MeRIP-seq:(Medium) rs61794768 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111210 RMVar_ID_111210 Human_SNP_ID_856663716 m1A Human chr4 + 173371121 173371121 173371121 GTGCAGAGTGAATTGCCGCTGCCGGAGCGGAGAGAGGCGGAGCGGCCAGGAGAGAGGGGATTTCT GTGCAGAGTGAATTGCCGCTGCCGGAGCGGAGGGAGGCGGAGCGGCCAGGAGAGAGGGGATTTCT A G SAP30 Ensembl:ENSG00000164105 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:173370987..173371500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_4795185,Human_RBP_ID_8943706,Human_RBP_ID_26350410 Human_Splice_Rec_623166 111211 RMVar_ID_111211 Human_SNP_ID_856670673 m1A Human chr4 - 49648693 49648693 49648693 CCGTTCCTTTCCATTCCATTCCATTCCATTCCATTCCGTTCCGTTCCATTCCATTCGTGTTGATT CCGTTCCTTTCCATTCCATTCCATTCCATTCCGTTCCGTTCCGTTCCATTCCATTCGTGTTGATT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr4:49648613..49648770 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 111212 RMVar_ID_111212 Human_SNP_ID_856685898 m1A Human chr4 + 145542630 145542630 145542630 TGCTTACCTGCCTCCTGAAGACCCCATGACCCAGGATGGCTCTCAGCCGATGGACACAAACATGA TGCTTACCTGCCTCCTGAAGACCCCATGACCCGGGATGGCTCTCAGCCGATGGACACAAACATGA A G SMAD1 Ensembl:ENSG00000170365 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr4:145542546..145542632 26863196 MeRIP-seq:(Medium) rs746555376 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_Splice_Rec_612402,Human_Splice_Rec_612403,Human_Splice_Rec_612426,Human_Splice_Rec_612427,Human_Splice_Rec_612438,Human_Splice_Rec_612439 Human_miRNA_ID_2039091,Human_miRNA_ID_3018071 RMVar_hsa_circ_228858,RMVar_hsa_circ_81302,RMVar_hsa_circ_358346,RMVar_hsa_circ_110653,RMVar_hsa_circ_228859,RMVar_hsa_circ_228860 111213 RMVar_ID_111213 Human_SNP_ID_856711761 m1A Human chr4 + 112644718 112644718 112644718 GAAATCAGGAAAAGGTAATGGAAGAAGAAAGCACTGAAAAGAAAAAAGAAGTTGAAAAAAAGAAA GAAATCAGGAAAAGGTAATGGAAGAAGAAAGCGCTGAAAAGAAAAAAGAAGTTGAAAAAAAGAAA A G LARP7 Ensembl:ENSG00000174720 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:112644637..112644725;chr4:112644634..112644775;chr4:112644616..112644800;chr4:112644618..112644774 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_72148,Human_RBP_ID_1971949,Human_RBP_ID_2814133,Human_RBP_ID_4770538,Human_RBP_ID_9148983,Human_RBP_ID_9349224,Human_RBP_ID_24547723,Human_RBP_ID_26349508,Human_RBP_ID_27824348 Human_Splice_Rec_593492,Human_Splice_Rec_593502,Human_Splice_Rec_593526,Human_Splice_Rec_593527,Human_Splice_Rec_593550,Human_Splice_Rec_593576,Human_Splice_Rec_593582,Human_Splice_Rec_593594,Human_Splice_Rec_593606,Human_Splice_Rec_593630,Human_Splice_Rec_593631,Human_Splice_Rec_593640 RMVar_hsa_circ_61736,RMVar_hsa_circ_228045,RMVar_hsa_circ_106189,RMVar_hsa_circ_228047,RMVar_hsa_circ_228046,RMVar_hsa_circ_69504 111214 RMVar_ID_111214 Human_SNP_ID_856711765 m1A Human chr4 + 112644718 112644718 112644718 GAAATCAGGAAAAGGTAATGGAAGAAGAAAGCACTGAAAAGAAAAAAGAAGTTGAAAAAAAGAAA GAAATCAGGAAAAGGTAATGGAAGAAGAAAGCCCTGAAAAGAAAAAAGAAGTTGAAAAAAAGAAA A C LARP7 Ensembl:ENSG00000174720 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr4:112644637..112644725;chr4:112644634..112644775;chr4:112644616..112644800;chr4:112644618..112644774 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_72148,Human_RBP_ID_1971949,Human_RBP_ID_2814133,Human_RBP_ID_4770538,Human_RBP_ID_9148983,Human_RBP_ID_9349224,Human_RBP_ID_24547723,Human_RBP_ID_26349508,Human_RBP_ID_27824348 Human_Splice_Rec_593492,Human_Splice_Rec_593502,Human_Splice_Rec_593526,Human_Splice_Rec_593527,Human_Splice_Rec_593550,Human_Splice_Rec_593576,Human_Splice_Rec_593582,Human_Splice_Rec_593594,Human_Splice_Rec_593606,Human_Splice_Rec_593630,Human_Splice_Rec_593631,Human_Splice_Rec_593640 RMVar_hsa_circ_61736,RMVar_hsa_circ_228045,RMVar_hsa_circ_106189,RMVar_hsa_circ_228047,RMVar_hsa_circ_228046,RMVar_hsa_circ_69504 111215 RMVar_ID_111215 Human_SNP_ID_832235277 m1A Human chr19 - 3762765 3762765 3762765 GGGCCAGGAGTCTTCCGGAAGTGGCGGGGTTTAGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTC GGGCCAGGAGTCTTCCGGAAGTGGCGGGGTTTCGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:3762687..3762833 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - 111216 RMVar_ID_111216 Human_SNP_ID_832236066 m1A Human chr19 + 53441815 53441815 53441815 TTCATAATCACAGAGAGGAGTCTGCAATGCCGAGTGGAGGAAGGAGGAACCGGAGTGTGAGCAGT TTCATAATCACAGAGAGGAGTCTGCAATGCCGTGTGGAGGAAGGAGGAACCGGAGTGTGAGCAGT A T TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:53441795..53441998 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_1575477,Human_RBP_ID_3589220,Human_RBP_ID_5099463,Human_RBP_ID_5586484,Human_RBP_ID_5651176,Human_RBP_ID_6782752,Human_RBP_ID_8728462,Human_RBP_ID_13543291,Human_RBP_ID_17387759,Human_RBP_ID_17502755,Human_RBP_ID_18533050,Human_RBP_ID_21960176,Human_RBP_ID_23806409,Human_RBP_ID_26338222 Human_Splice_Rec_2041110 RMVar_hsa_circ_311675 111217 RMVar_ID_111217 Human_SNP_ID_832238328 m1A Human chr19 + 52222221 52222221 52222221 CGCTTCAATGTGGCCAAGTCTCTGCAGAAGATAGGGCCCATCCTGGACAACAGGTGAGGTCTGGA CGCTTCAATGTGGCCAAGTCTCTGCAGAAGATTGGGCCCATCCTGGACAACAGGTGAGGTCTGGA A T PPP2R1A Ensembl:ENSG00000105568 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:52222176..52225840 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_279898,Human_RBP_ID_526272,Human_RBP_ID_1017898,Human_RBP_ID_1891409,Human_RBP_ID_6781576,Human_RBP_ID_9089458,Human_RBP_ID_13504270,Human_RBP_ID_17270453,Human_RBP_ID_22449644,Human_RBP_ID_27473616 Human_Splice_Rec_2039281,Human_Splice_Rec_2039319,Human_Splice_Rec_2039349 RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_127662,RMVar_hsa_circ_127787,RMVar_hsa_circ_97176,RMVar_hsa_circ_196085,RMVar_hsa_circ_369728,RMVar_hsa_circ_196084,RMVar_hsa_circ_372981,RMVar_hsa_circ_122127,RMVar_hsa_circ_196091,RMVar_hsa_circ_196092,RMVar_hsa_circ_196093,RMVar_hsa_circ_122250,RMVar_hsa_circ_196094,RMVar_hsa_circ_196096,RMVar_hsa_circ_322193,RMVar_hsa_circ_196098,RMVar_hsa_circ_196102,RMVar_hsa_circ_309744,RMVar_hsa_circ_279840,RMVar_hsa_circ_196101,RMVar_hsa_circ_126910,RMVar_hsa_circ_77928,RMVar_hsa_circ_196104,RMVar_hsa_circ_324394,RMVar_hsa_circ_196105,RMVar_hsa_circ_196106,RMVar_hsa_circ_196109,RMVar_hsa_circ_112824,RMVar_hsa_circ_292359,RMVar_hsa_circ_196108 111218 RMVar_ID_111218 Human_SNP_ID_832242007 m1A Human chr19 - 10319242 10319242 10319242 TCCAACCCAATGTGCTTCTCCCGCTTTCATTCAGGACATGGGACCTCGGCGGCTCTTCTCCCACC TCCAACCCAATGTGCTTCTCCCGCTTTCATTCGGGACATGGGACCTCGGCGGCTCTTCTCCCACC T C RAVER1,AC011511.4 Ensembl:ENSG00000161847,Ensembl:ENSG00000267303 Protein coding,Protein coding intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:10319226..10319250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_4498176,Human_RBP_ID_9328584,Human_RBP_ID_19092131 Human_Splice_Rec_1954179,Human_Splice_Rec_1954209,Human_Splice_Rec_1954227,Human_Splice_Rec_1954251,Human_Splice_Rec_1954279,Human_Splice_Rec_1954291 RMVar_hsa_circ_38589 111219 RMVar_ID_111219 Human_SNP_ID_832242971 m1A Human chr19 + 3530455 3530455 3530455 CATGGGAGAGCGGATGGGAGAGCGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGG CATGGGAGAGCGGATGGGAGAGCGCATGGGAGGGCGCATGGATGAGCGCATGGGAGAGCGCATGG A G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3530451..3530525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_5292615,Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 111220 RMVar_ID_111220 Human_SNP_ID_832244040 m1A Human chr19 - 3404335 3404335 3404335 GCAAGGTTAAAAATACCCGCACGCACACCCTCACCCCCACCCCCTCCCGGTCCCGCCAATGTCAA GCAAGGTTAAAAATACCCGCACGCACACCCTCCCCCCCACCCCCTCCCGGTCCCGCCAATGTCAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:3404332..3404533;chr19:3404329..3404640 26863196 MeRIP-seq:(Medium) rs955085827 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 111221 RMVar_ID_111221 Human_SNP_ID_832251217 m1A Human chr19 - 1650241 1650241 1650241 AGGTGCCCGCCCTGGCCCCAGGAGAATGAACCAGCCGCAGAGGATGGCGCCTGTGGGCACAGACA AGGTGCCCGCCCTGGCCCCAGGAGAATGAACCGGCCGCAGAGGATGGCGCCTGTGGGCACAGACA T C TCF3 Ensembl:ENSG00000071564 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1650135..1650333 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_515207,Human_RBP_ID_3955823,Human_RBP_ID_4507943,Human_RBP_ID_9293153 Human_Splice_Rec_1933497,Human_Splice_Rec_1933534,Human_Splice_Rec_1933535,Human_Splice_Rec_1933574,Human_Splice_Rec_1933575,Human_Splice_Rec_1933610,Human_Splice_Rec_1933611,Human_Splice_Rec_1933664,Human_Splice_Rec_1933665,Human_Splice_Rec_1933738,Human_Splice_Rec_1933739,Human_Splice_Rec_1933813,Human_Splice_Rec_1933823 RMVar_hsa_circ_32582,RMVar_hsa_circ_99682,RMVar_hsa_circ_191107,RMVar_hsa_circ_191113,RMVar_hsa_circ_355282,RMVar_hsa_circ_191115,RMVar_hsa_circ_286176 111222 RMVar_ID_111222 Human_SNP_ID_832259548 m1A Human chr19 + 55083408 55083408 55083408 AGGCTGGAGCTGTCCCCGGAGGAGGGACCCCCATACAGACCCGAGTTCTTCAGCGGCTGGGAGCC AGGCTGGAGCTGTCCCCGGAGGAGGGACCCCCGTACAGACCCGAGTTCTTCAGCGGCTGGGAGCC A G EPS8L1 Ensembl:ENSG00000131037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55083400..55083600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine Human_Splice_Rec_2045686,Human_Splice_Rec_2045714,Human_Splice_Rec_2045742,Human_Splice_Rec_2045786,Human_Splice_Rec_2045820,Human_Splice_Rec_2045830,Human_Splice_Rec_2045856,Human_Splice_Rec_2045882,Human_Splice_Rec_2045888,Human_Splice_Rec_2045894,Human_Splice_Rec_2045912 111223 RMVar_ID_111223 Human_SNP_ID_832260329 m1A Human chr19 + 33302359 33302359 33302359 CGGCGCTGCTGGGCGCGTGCGGGGGGCTCTGCAGGTGGCTGCTCATCGGGGGCCGCGGCTCCGCC CGGCGCTGCTGGGCGCGTGCGGGGGGCTCTGCTGGTGGCTGCTCATCGGGGGCCGCGGCTCCGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:33302113..33302492 26863196 MeRIP-seq:(Medium) rs1315626965 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 111224 RMVar_ID_111224 Human_SNP_ID_832262879 m1A Human chr19 + 4012932 4012932 4012932 TGTGTGTGCTTGCTCCTCCTCAGAACATGGTGATGAGTTTTCGAGTCTCCGACCTTCAGATGCTC TGTGTGTGCTTGCTCCTCCTCAGAACATGGTGCTGAGTTTTCGAGTCTCCGACCTTCAGATGCTC A C PIAS4 Ensembl:ENSG00000105229 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4012928..4013153 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_4557923,Human_RBP_ID_18732590 Human_Splice_Rec_1938868,Human_Splice_Rec_1938888,Human_Splice_Rec_1938894,Human_Splice_Rec_1938900 RMVar_hsa_circ_44291,RMVar_hsa_circ_376796,RMVar_hsa_circ_48372,RMVar_hsa_circ_191488 111225 RMVar_ID_111225 Human_SNP_ID_832268383 m1A Human chr19 - 42248778 42248778 42248778 GTCGGAGGAGGTAGAGGTGACTGACATCAGTGATGAGGATGAGGAAGACGGGGAGGTGTTCAAGA GTCGGAGGAGGTAGAGGTGACTGACATCAGTGCTGAGGATGAGGAAGACGGGGAGGTGTTCAAGA T G ERF,AC006486.1 Ensembl:ENSG00000105722,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:42248776..42248875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_6766966,Human_RBP_ID_13463680,Human_RBP_ID_23799401,Human_RBP_ID_27468676 Human_miRNA_ID_208481 111226 RMVar_ID_111226 Human_SNP_ID_832271327 m1A Human chr19 + 1419807 1419807 1419807 TCACCCCACGCACACACTCATGAAACCATCCCAACCGTCACGGCAGCGAGCACTCACCCCACGCA TCACCCCACGCACACACTCATGAAACCATCCCGACCGTCACGGCAGCGAGCACTCACCCCACGCA A G DAZAP1 Ensembl:ENSG00000071626 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1419804..1419934 26863196 MeRIP-seq:(Medium) rs1212828228 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_202987,Human_RBP_ID_9425058,Human_RBP_ID_13375805,Human_RBP_ID_24532727 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_331845,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_369637,RMVar_hsa_circ_107704,RMVar_hsa_circ_191054,RMVar_hsa_circ_191056,RMVar_hsa_circ_191057,RMVar_hsa_circ_191058,RMVar_hsa_circ_191055,RMVar_hsa_circ_85965,RMVar_hsa_circ_106290,RMVar_hsa_circ_121986,RMVar_hsa_circ_191059,RMVar_hsa_circ_191060,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_191061 111227 RMVar_ID_111227 Human_SNP_ID_832272253 m1A Human chr19 - 19305878 19305878 19305878 TGTCTTCCAGTCCCCTGACGAGGACGAGGAGGAGGACTATGAGCAGTGGCTGGAGATCAAAGGTA TGTCTTCCAGTCCCCTGACGAGGACGAGGAGGTGGACTATGAGCAGTGGCTGGAGATCAAAGGTA T A SUGP1 Ensembl:ENSG00000105705 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:19305867..19310185 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_911073,Human_RBP_ID_18440804,Human_RBP_ID_18994708,Human_RBP_ID_19089805,Human_RBP_ID_22977710,Human_RBP_ID_27815332 Human_Splice_Rec_1983009,Human_Splice_Rec_1983049,Human_Splice_Rec_1983073,Human_Splice_Rec_1983109,Human_Splice_Rec_1983123,Human_Splice_Rec_1983135,Human_Splice_Rec_1983145,Human_Splice_Rec_1983155,Human_Splice_Rec_1983161 111228 RMVar_ID_111228 Human_SNP_ID_832272895 m1A Human chr19 + 3981963 3981963 3981963 CGCAGCCCTCACTCACCTTGAAGATGGGGTCCAGGATCAGCTGGCAGAAGGTGCGTGGCAGCTTC CGCAGCCCTCACTCACCTTGAAGATGGGGTCCGGGATCAGCTGGCAGAAGGTGCGTGGCAGCTTC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:3981951..3982000 26863196 MeRIP-seq:(Medium) rs1204833430 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck 111229 RMVar_ID_111229 Human_SNP_ID_832274906 m1A Human chr19 + 10500059 10500059 10500059 GCTGCATGGGGTTCCAGAAGATAAGCAACACCACCACCTCTGGCACTCAGGGACCTGGAGGGGAG GCTGCATGGGGTTCCAGAAGATAAGCAACACCGCCACCTCTGGCACTCAGGGACCTGGAGGGGAG A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:10499959..10500100 26863410 MeRIP-seq:(Medium) rs966252738 Functional Loss SNV ICGC,COSMIC 33..33 33 READ,large_intestine adenocarcinoma 3 large intestine 111230 RMVar_ID_111230 Human_SNP_ID_832282737 m1A Human chr19 + 49658435 49658434 49658435 CCCTGGCCAGCTCTTCGCCCCTCACCTCTTTGAAACTCTGGACGTATTTATGGCTCCACCTCCCC CCCTGGCCAGCTCTTCGCCCCTCACCTCTTTG_AACTCTGGACGTATTTATGGCTCCACCTCCCC GA G SCAF1 Ensembl:ENSG00000126461 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49658384..49658569 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 MALY 1 - Human_RBP_ID_525447,Human_RBP_ID_1890987,Human_RBP_ID_3575174,Human_RBP_ID_5117059,Human_RBP_ID_5469065,Human_RBP_ID_17657298,Human_RBP_ID_18947244,Human_RBP_ID_23804653,Human_RBP_ID_27277187,Human_RBP_ID_27470473 111231 RMVar_ID_111231 Human_SNP_ID_832284842 m1A Human chr19 - 29812097 29812076 29812097 GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCGACGGCAGTGGCGGCGGCGGCGCCGGGAGTCGGC GCGCGCTCCAGTCCCGGCAGGCGGCGGCGGCG_____________________CCGGGAGTCGGC GCGCCGCCGCCGCCACTGCCGT G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:29811947..29812577 26863410 MeRIP-seq:(Medium) rs998974050 Functional Loss DEL ICGC 33..53 33 PBCA 1 - 111232 RMVar_ID_111232 Human_SNP_ID_832287906 m1A Human chr19 + 49101463 49101463 49101463 CTATGCCTTCATCGAGTACGAACACGAGCGAGACATGCACTGTGAGTACCTCCCGCCGAGCCCTG CTATGCCTTCATCGAGTACGAACACGAGCGAGGCATGCACTGTGAGTACCTCCCGCCGAGCCCTG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1569549,Human_RBP_ID_1890862,Human_RBP_ID_3957312,Human_RBP_ID_13494335,Human_RBP_ID_19090640,Human_RBP_ID_22975167,Human_RBP_ID_23114782,Human_RBP_ID_26338423,Human_RBP_ID_27276913 Human_Splice_Rec_2028572,Human_Splice_Rec_2028573,Human_Splice_Rec_2028590,Human_Splice_Rec_2028591,Human_Splice_Rec_2028610,Human_Splice_Rec_2028611,Human_Splice_Rec_2028628,Human_Splice_Rec_2028629,Human_Splice_Rec_2028648,Human_Splice_Rec_2028649,Human_Splice_Rec_2028666,Human_Splice_Rec_2028667,Human_Splice_Rec_2028692 RMVar_hsa_circ_94057,RMVar_hsa_circ_195804,RMVar_hsa_circ_333511,RMVar_hsa_circ_195805 111233 RMVar_ID_111233 Human_SNP_ID_832296791 m1A Human chr19 + 4792728 4792728 4792728 TGAACGGGGAATCTTACGAAAGCTGCTGTCCCACCAGCCGGGAAGCTGCCGTGGAAGCCTTGGAA TGAACGGGGAATCTTACGAAAGCTGCTGTCCCGCCAGCCGGGAAGCTGCCGTGGAAGCCTTGGAA A G FEM1A Ensembl:ENSG00000141965 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:4792679..4792880 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4539840,Human_RBP_ID_8838948,Human_RBP_ID_22069545 111234 RMVar_ID_111234 Human_SNP_ID_832303141 m1A Human chr19 - 2431872 2431872 2431872 AGGTGTGGGCAGCTGGTGCGGGGGTGGCCCACAGCCCCCCCTCGACGCTGGTGTGGAAGGGCCAG AGGTGTGGGCAGCTGGTGCGGGGGTGGCCCACGGCCCCCCCTCGACGCTGGTGTGGAAGGGCCAG T C LMNB2 Ensembl:ENSG00000176619 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2431851..2431875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_518238,Human_RBP_ID_1239760,Human_RBP_ID_9293191,Human_RBP_ID_17918862 Human_Splice_Rec_1935832,Human_Splice_Rec_1935833,Human_Splice_Rec_1935854,Human_Splice_Rec_1935855,Human_Splice_Rec_1935859 RMVar_hsa_circ_79017,RMVar_hsa_circ_97104,RMVar_hsa_circ_115714,RMVar_hsa_circ_120423,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191264,RMVar_hsa_circ_191263,RMVar_hsa_circ_191261,RMVar_hsa_circ_378009,RMVar_hsa_circ_191259,RMVar_hsa_circ_191266 111235 RMVar_ID_111235 Human_SNP_ID_832303144 m1A Human chr19 - 2431872 2431872 2431872 AGGTGTGGGCAGCTGGTGCGGGGGTGGCCCACAGCCCCCCCTCGACGCTGGTGTGGAAGGGCCAG AGGTGTGGGCAGCTGGTGCGGGGGTGGCCCACTGCCCCCCCTCGACGCTGGTGTGGAAGGGCCAG T A LMNB2 Ensembl:ENSG00000176619 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:2431851..2431875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_518238,Human_RBP_ID_1239760,Human_RBP_ID_9293191,Human_RBP_ID_17918862 Human_Splice_Rec_1935832,Human_Splice_Rec_1935833,Human_Splice_Rec_1935854,Human_Splice_Rec_1935855,Human_Splice_Rec_1935859 RMVar_hsa_circ_79017,RMVar_hsa_circ_97104,RMVar_hsa_circ_115714,RMVar_hsa_circ_120423,RMVar_hsa_circ_97984,RMVar_hsa_circ_96966,RMVar_hsa_circ_191260,RMVar_hsa_circ_191262,RMVar_hsa_circ_191264,RMVar_hsa_circ_191263,RMVar_hsa_circ_191261,RMVar_hsa_circ_378009,RMVar_hsa_circ_191259,RMVar_hsa_circ_191266 111236 RMVar_ID_111236 Human_SNP_ID_832303371 m1A Human chr19 - 57571767 57571767 57571767 TAAGGGGAATTCCTTCCCTTTTCTGACTGATTACAGCATACATCTGACCAGTTTTGGCCAGAAGG TAAGGGGAATTCCTTCCCTTTTCTGACTGATTGCAGCATACATCTGACCAGTTTTGGCCAGAAGG T C ZNF416 Ensembl:ENSG00000083817 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:57571708..57571807 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_8495052 111237 RMVar_ID_111237 Human_SNP_ID_832303524 m1A Human chr19 - 51345365 51345362 51345365 GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGAAGATCGAGGTGATCAAGCCTGGGGACCTGGGTG GGCTTCCCATGTGCAGAAAGCCAAGAAGAAGA___TCGAGGTGATCAAGCCTGGGGACCTGGGTG ATCT A ETFB Ensembl:ENSG00000105379 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:51345237..51345440 26863196 MeRIP-seq:(Medium) rs767519060 Functional Loss DEL ICGC 33..35 33 STAD 1 - Human_RBP_ID_17656339,Human_RBP_ID_18738281,Human_RBP_ID_18998656,Human_RBP_ID_22447974,Human_RBP_ID_22763127,Human_RBP_ID_26336676 Human_Splice_Rec_2037910,Human_Splice_Rec_2037920,Human_Splice_Rec_2037928 111238 RMVar_ID_111238 Human_SNP_ID_832304145 m1A Human chr19 - 38900043 38900043 38900043 CATCTGCGTCGGCAGCTTTTCCCAAGCACGCGACCCCAGCCATGGCCCCCGCCGCCTCAGGGGCC CATCTGCGTCGGCAGCTTTTCCCAAGCACGCGCCCCCAGCCATGGCCCCCGCCGCCTCAGGGGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38899995..38900143 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111239 RMVar_ID_111239 Human_SNP_ID_832304413 m1A Human chr19 + 8445027 8445027 8445027 GAAAATGGCGGCAGGGGTCGAAGCGGCGGCGGAGGTGGCGGCGACGGAGATCAAAATGGAGGAAG GAAAATGGCGGCAGGGGTCGAAGCGGCGGCGGGGGTGGCGGCGACGGAGATCAAAATGGAGGAAG A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:8444976..8445149 26863196 MeRIP-seq:(Medium) rs767113114 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 12 haematopoietic and lymphoid tissue Human_RBP_ID_54991,Human_RBP_ID_4555679,Human_RBP_ID_9380263,Human_RBP_ID_18165939,Human_RBP_ID_23114716,Human_RBP_ID_26335442,Human_RBP_ID_27815014 Human_Splice_Rec_1950135,Human_Splice_Rec_1950167,Human_Splice_Rec_1950173,Human_Splice_Rec_1950199,Human_Splice_Rec_1950229,Human_Splice_Rec_1950255,Human_Splice_Rec_1950281,Human_Splice_Rec_1950301,Human_Splice_Rec_1950315 111240 RMVar_ID_111240 Human_SNP_ID_832306199 m1A Human chr19 + 12734364 12734364 12734364 GGACCGCCCTTCCTCTTCGGATCCCCGGGGCCAGCGGCGGCGGCCGACTGGTCGGGTCGCTGCGG GGACCGCCCTTCCTCTTCGGATCCCCGGGGCCGGCGGCGGCGGCCGACTGGTCGGGTCGCTGCGG A G RF00017-1166,RF00017-1304 RNACentral:URS00009832A9,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12734301..12734650 32194978 MeRIP-seq:(Medium) rs1201211736 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 111241 RMVar_ID_111241 Human_SNP_ID_832308590 m1A Human chr19 + 52143209 52143209 52143209 AAAGTATAACTGGAGTGCCAAGGCTAAAAGACAAAATACCACCGGAACTGGTGGAATGAGGCACC AAAGTATAACTGGAGTGCCAAGGCTAAAAGACGAAATACCACCGGAACTGGTGGAATGAGGCACC A G AC011468.3,RPL37P23 Ensembl:ENSG00000268458,Ensembl:ENSG00000243680 lincRNA,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs756302885 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_26475143 Human_miRNA_ID_1877777 111242 RMVar_ID_111242 Human_SNP_ID_832309224 m1A Human chr19 - 50480217 50480217 50480217 GGGAGAAGGGGGCTCATCCCCGACACCAACTCACCGCAGGGACAAAGGAGGAGACATAGCCACCA GGGAGAAGGGGGCTCATCCCCGACACCAACTCGCCGCAGGGACAAAGGAGGAGACATAGCCACCA T C AC020909.3 Ensembl:ENSG00000268854 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:50480201..50480225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111243 RMVar_ID_111243 Human_SNP_ID_832315616 m1A Human chr19 + 7099006 7099006 7099006 CTGGGCGAGGGGAGCCAAAGACGGGTGGTGGGAGCCGAGGTCGGCCGAGAGGAACCGGAAAAGCC CTGGGCGAGGGGAGCCAAAGACGGGTGGTGGGTGCCGAGGTCGGCCGAGAGGAACCGGAAAAGCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7098957..7099711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111244 RMVar_ID_111244 Human_SNP_ID_832316141 m1A Human chr19 + 34227830 34227822 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTG________TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1438954605 Functional Loss DEL TCGA 26..33 33 UCEC 1 - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 111245 RMVar_ID_111245 Human_SNP_ID_832322058 m1A Human chr19 + 37469483 37469483 37469483 GATCTTCCACCAGTTCTGTTCTGCAGGTCGGGAGTGGGCTGAGGAGTGGCGTGTGGGTCTCCGGA GATCTTCCACCAGTTCTGTTCTGCAGGTCGGGGGTGGGCTGAGGAGTGGCGTGTGGGTCTCCGGA A G ZNF570 Ensembl:ENSG00000171827 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:37469388..37469501 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_520906,Human_RBP_ID_6756571 Human_Splice_Rec_1999914,Human_Splice_Rec_1999915,Human_Splice_Rec_1999918,Human_Splice_Rec_1999919,Human_Splice_Rec_1999927,Human_Splice_Rec_1999929,Human_Splice_Rec_1999937,Human_Splice_Rec_1999943 111246 RMVar_ID_111246 Human_SNP_ID_832322659 m1A Human chr19 - 12699464 12699464 12699464 TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTAAAAAAAAACTATTTAATTTTTTAATTTATTTT TTCTTCTCGTTTTCCTTTTTTTTTTTTTTTTTTAAAAAAAACTATTTAATTTTTTAATTTATTTT T A TNPO2 Ensembl:ENSG00000105576 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs868115219 Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_6720738,Human_RBP_ID_22966817 111247 RMVar_ID_111247 Human_SNP_ID_832324800 m1A Human chr19 - 3192611 3192611 3192611 GCACGGCGGCCATGGCCCTGGGCAGGATGATGACCACGGCGCCCGCCGACTGCCGCAGGGCCTTC GCACGGCGGCCATGGCCCTGGGCAGGATGATGCCCACGGCGCCCGCCGACTGCCGCAGGGCCTTC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:3192513..3193400 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 111248 RMVar_ID_111248 Human_SNP_ID_832331841 m1A Human chr19 - 48390510 48390510 48390510 TCTGTCTCTGGACCACAGGAATTTCAGGGAAGAGCCAGGTCCTGTTTGCTGTGGTGTTCACTGCC TCTGTCTCTGGACCACAGGAATTTCAGGGAAGCGCCAGGTCCTGTTTGCTGTGGTGTTCACTGCC T G KDELR1 Ensembl:ENSG00000105438 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:48390426..48390577 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_53342,Human_RBP_ID_524856,Human_RBP_ID_4559780,Human_RBP_ID_6777596,Human_RBP_ID_17271917,Human_RBP_ID_17386947,Human_RBP_ID_17928945,Human_RBP_ID_20431908,Human_RBP_ID_22446905 Human_Splice_Rec_2026484,Human_Splice_Rec_2026485,Human_Splice_Rec_2026491,Human_Splice_Rec_2026498,Human_Splice_Rec_2026499,Human_Splice_Rec_2026504,Human_Splice_Rec_2026505,Human_Splice_Rec_2026508 Human_miRNA_ID_2084429,Human_miRNA_ID_2883513 RMVar_hsa_circ_6494,RMVar_hsa_circ_195681,RMVar_hsa_circ_102908,RMVar_hsa_circ_195682 111249 RMVar_ID_111249 Human_SNP_ID_832332349 m1A Human chr19 + 54453655 54453655 54453655 ATCCGCACCCCAACACCAAGGGACTCTGAACCAGGTAACATCCTAGCCCAGCTCCCATACCCTGC ATCCGCACCCCAACACCAAGGGACTCTGAACCCGGTAACATCCTAGCCCAGCTCCCATACCCTGC A C LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54453568..54453692 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_3957481,Human_RBP_ID_13507684 Human_Splice_Rec_2043811,Human_Splice_Rec_2043841,Human_Splice_Rec_2043889 111250 RMVar_ID_111250 Human_SNP_ID_832332407 m1A Human chr19 + 55401601 55401601 55401601 GAGGAAGCTTCAGTGCCACTGGCCAGGGCCCGACCGGCTTCGGCCCTGCCGCTGGGCCCGCCGGC GAGGAAGCTTCAGTGCCACTGGCCAGGGCCCGCCCGGCTTCGGCCCTGCCGCTGGGCCCGCCGGC A C RPL28 Ensembl:ENSG00000108107 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:55401501..55401646 26863410 MeRIP-seq:(Medium) rs111954966 Functional Loss SNV ICGC 33..33 33 COCA 1 - 111251 RMVar_ID_111251 Human_SNP_ID_832332627 m1A Human chr19 - 44878315 44878315 44878315 CCTCCTCACCCTCAGCAGGATGAAGGCCAAGGACCCCCCAGCCAGAAGCAGCAGCACCAGCAGTG CCTCCTCACCCTCAGCAGGATGAAGGCCAAGGCCCCCCCAGCCAGAAGCAGCAGCACCAGCAGTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:44878266..44878367 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111252 RMVar_ID_111252 Human_SNP_ID_832336137 m1A Human chr19 + 2353208 2353208 2353208 GTCCCCGGTAACCCAGCCTGGCGCCTCGGCCTAGGGGAGGGGTGAGACGCTCGCTGCCGTGCCCG GTCCCCGGTAACCCAGCCTGGCGCCTCGGCCTGGGGGAGGGGTGAGACGCTCGCTGCCGTGCCCG A G SPPL2B Ensembl:ENSG00000005206 Protein coding stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2353160..2353909 32194978 MeRIP-seq:(Medium) rs888585423 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 20 head and neck,large intestine Human_RBP_ID_4514347,Human_RBP_ID_26471678 RMVar_hsa_circ_84366,RMVar_hsa_circ_94701,RMVar_hsa_circ_191257,RMVar_hsa_circ_191258 111253 RMVar_ID_111253 Human_SNP_ID_832337801 m1A Human chr19 + 48965471 48965471 48965471 TCGGCCATCTCCTGCTTCTGGGACCTGCCAGCACCGTTTTTGTGGTTAGCTCCTTCTTGCCAACC TCGGCCATCTCCTGCTTCTGGGACCTGCCAGCGCCGTTTTTGTGGTTAGCTCCTTCTTGCCAACC A G FTL Ensembl:ENSG00000087086 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:48965370..48965483 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_525123,Human_RBP_ID_17272740,Human_RBP_ID_17386989,Human_RBP_ID_27470192 Human_miRNA_ID_2358391,Human_miRNA_ID_3060827 RMVar_hsa_circ_76881,RMVar_hsa_circ_123826,RMVar_hsa_circ_113700,RMVar_hsa_circ_195753,RMVar_hsa_circ_195754,RMVar_hsa_circ_195752 111254 RMVar_ID_111254 Human_SNP_ID_832339081 m1A Human chr19 + 50506240 50506240 50506240 CCTCCTTGGTCACTACCAGCAGCACCTCGCACAGGCCCTGGGCCAGCGCAGCCGCCAGGAAGGCC CCTCCTTGGTCACTACCAGCAGCACCTCGCACCGGCCCTGGGCCAGCGCAGCCGCCAGGAAGGCC A C lnc-EMC10-4 RNACentral:URS00009B4BE6 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50506070..50506275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 111255 RMVar_ID_111255 Human_SNP_ID_832343984 m1A Human chr19 - 54461629 54461629 54461629 AAGAATGCGGAGAGGGAGGGAGGGAAAGGGGAAAAAAAAATCAGAAGAAACACTGGGGGCAGAGG AAGAATGCGGAGAGGGAGGGAGGGAAAGGGGAGAAAAAAATCAGAAGAAACACTGGGGGCAGAGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:54461530..54461756 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 111256 RMVar_ID_111256 Human_SNP_ID_832347881 m1A Human chr19 + 4099269 4099260 4099269 AGATGCTGTGAGGCTCTCCTTCTTCCCCGTCGACCACGGGCCGGCCAAAGATGGCCTCCAGCTCT AGATGCTGTGAGGCTCTCCTTCTT_________CCACGGGCCGGCCAAAGATGGCCTCCAGCTCT TCCCCGTCGA T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4097276..4099400 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 25..33 33 BOCA 1 - 111257 RMVar_ID_111257 Human_SNP_ID_832350879 m1A Human chr19 + 3976488 3976488 3976488 GTGTCGGGACAGTCTCCAGGTGTCGTCTGAGAATTCGAGGACGTGGTGCTGTGGGTGCTGCGAGT GTGTCGGGACAGTCTCCAGGTGTCGTCTGAGATTTCGAGGACGTGGTGCTGTGGGTGCTGCGAGT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3976094..3976773 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 2 kidney RMVar_hsa_circ_191443,RMVar_hsa_circ_191445 111258 RMVar_ID_111258 Human_SNP_ID_832360145 m1A Human chr19 + 40280616 40280616 40280616 CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCAGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC CAGTGAAAGGGCCCTGCCTGCCCCGCAGCCCCCGGACTCATCTCCTCCCTGCTCCCTCGCTCTGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40280613..40280801 26863196 MeRIP-seq:(Medium) rs8102171 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 3 brain GWAS_ID_10097,GWAS_ID_10098,GWAS_ID_10099,GWAS_ID_10100,GWAS_ID_10101,GWAS_ID_10102,GWAS_ID_10103,GWAS_ID_10104,GWAS_ID_10105,GWAS_ID_10106,GWAS_ID_10107,GWAS_ID_10108,GWAS_ID_10109,GWAS_ID_10110 111259 RMVar_ID_111259 Human_SNP_ID_832360146 m1A Human chr19 + 2802475 2802475 2802475 ACACCTCCCGACACCCCCACCTCCCGACACCAACACCTCCCGACACCAACACCTCCCGACACCAA ACACCTCCCGACACCCCCACCTCCCGACACCACCACCTCCCGACACCAACACCTCCCGACACCAA A C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2802473..2802624 26863196 MeRIP-seq:(Medium) rs1254390591 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 haematopoietic and lymphoid tissue Human_RBP_ID_26784984 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 111260 RMVar_ID_111260 Human_SNP_ID_832361489 m1A Human chr19 - 984390 984390 984390 CCACACGATGCAGCTCCACATCGGGGCCGCCGAGTCCGTACACACGGCCACCTCCATGGGCGCCG CCACACGATGCAGCTCCACATCGGGGCCGCCGTGTCCGTACACACGGCCACCTCCATGGGCGCCG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:984326..984550;chr19:984326..984575 26863196 MeRIP-seq:(Medium) rs1240900377 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 111261 RMVar_ID_111261 Human_SNP_ID_832361885 m1A Human chr19 - 829278 829278 829278 GTCCCTTCCCTTCTCTGAGCCTCCTCCATCTGACCCCCTCCCCTTCTCTGCACCTCCTCCATCTG GTCCCTTCCCTTCTCTGAGCCTCCTCCATCTGCCCCCCTCCCCTTCTCTGCACCTCCTCCATCTG T G HSALNG0122936 RNACentral:URS0000EA9395 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:828988..829580 26863196 MeRIP-seq:(Medium) rs1389925639 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111262 RMVar_ID_111262 Human_SNP_ID_832363373 m1A Human chr19 + 49595043 49595043 49595043 CCTTACCGCCCTGGCCCCCCAGACCCACCACCACCTCCTCGCCACCTCCCAACTCAGTTCAACCT CCTTACCGCCCTGGCCCCCCAGACCCACCACCCCCTCCTCGCCACCTCCCAACTCAGTTCAACCT A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49594993..49595190 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_miRNA_ID_2089251,Human_miRNA_ID_2090123 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111263 RMVar_ID_111263 Human_SNP_ID_832363376 m1A Human chr19 + 49595043 49595043 49595043 CCTTACCGCCCTGGCCCCCCAGACCCACCACCACCTCCTCGCCACCTCCCAACTCAGTTCAACCT CCTTACCGCCCTGGCCCCCCAGACCCACCACCGCCTCCTCGCCACCTCCCAACTCAGTTCAACCT A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49594993..49595190 26863196 MeRIP-seq:(Medium) rs1311260696 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_miRNA_ID_2089251,Human_miRNA_ID_2090123 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111264 RMVar_ID_111264 Human_SNP_ID_832365456 m1A Human chr19 - 11002975 11002975 11002975 GACACTGAGGTTGCAGGGCCTCCAGACCAAACACTTACAGAGGCCAAGGTGGGAAGCACCCACTC GACACTGAGGTTGCAGGGCCTCCAGACCAAACGCTTACAGAGGCCAAGGTGGGAAGCACCCACTC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11002973..11003215 26863196 MeRIP-seq:(Medium) rs17001078 Functional Loss SNV ICGC,COSMIC 33..33 33 meninges atypical,meninges choroid,meninges anaplastic,meninges meningothelial,meninges transitional,ESCA,meninges fibroblastic 542 brain GWAS_ID_9608,GWAS_ID_9609,GWAS_ID_9610,GWAS_ID_9611,GWAS_ID_9612,GWAS_ID_9613,GWAS_ID_9614,GWAS_ID_9615,GWAS_ID_9616,GWAS_ID_9617 111265 RMVar_ID_111265 Human_SNP_ID_832365769 m1A Human chr19 + 808642 808642 808642 CCAGAACGTGCAGCTGCCCCGCGAGGGCCAGGAGGACCAGGGCCTGACCAAGGACTACGGCAACT CCAGAACGTGCAGCTGCCCCGCGAGGGCCAGGTGGACCAGGGCCTGACCAAGGACTACGGCAACT A T PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:808601..808650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 30 liver Human_RBP_ID_1893729,Human_RBP_ID_5190861,Human_RBP_ID_8496906,Human_RBP_ID_13535154,Human_RBP_ID_18532677,Human_RBP_ID_20349825,Human_RBP_ID_22446263,Human_RBP_ID_22533053,Human_RBP_ID_26997777,Human_RBP_ID_27472819,Human_RBP_ID_27815715 Human_Splice_Rec_1928970,Human_Splice_Rec_1928982,Human_Splice_Rec_1929016,Human_Splice_Rec_1929046,Human_Splice_Rec_1929074,Human_Splice_Rec_1929102,Human_Splice_Rec_1929126,Human_Splice_Rec_1929154,Human_Splice_Rec_1929182,Human_Splice_Rec_1929198,Human_Splice_Rec_1929212,Human_Splice_Rec_1929220 RMVar_hsa_circ_24441,RMVar_hsa_circ_361069,RMVar_hsa_circ_27836,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_926,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 111266 RMVar_ID_111266 Human_SNP_ID_832366536 m1A Human chr19 + 1881581 1881581 1881581 CAGCGACAGCCCATTCATGGCGGGCGCCGCCCAGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA CAGCGACAGCCCATTCATGGCGGGCGCCGCCCGGGCCGGGCCTCCACCGGGGCCCCCGCCAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1881500..1881700;chr19:1881523..1881681;chr19:1881507..1881682;chr19:1881516..1881689 26863196 MeRIP-seq:(Medium) rs1358651175 Functional Loss SNV ICGC 33..33 33 COCA 1 - 111267 RMVar_ID_111267 Human_SNP_ID_832373307 m1A Human chr19 + 6212969 6212969 6212969 GCTAAGGCAGTGCTGCGGGCAGGCGAGACGGGAGAGGAGGGCAGGCGAGGCCTGGCTGCAGCCTC GCTAAGGCAGTGCTGCGGGCAGGCGAGACGGGGGAGGAGGGCAGGCGAGGCCTGGCTGCAGCCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:6212918..6213125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 111268 RMVar_ID_111268 Human_SNP_ID_832377907 m1A Human chr19 + 45778607 45778607 45778607 TCCGCTCCCCAAACTTGCTCAGCAGTGTCAGCAGGTCCCCGCCCACGTAATACTCCATGACCAGG TCCGCTCCCCAAACTTGCTCAGCAGTGTCAGCGGGTCCCCGCCCACGTAATACTCCATGACCAGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45778557..45778671 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 7 head and neck Human_RBP_ID_1132983 111269 RMVar_ID_111269 Human_SNP_ID_832384464 m1A Human chr19 - 55621184 55621184 55621184 AAGAGACTCTGGGATCCCATCACCTCAAAGCCAGAGGGTCCCCAAGTCACCGCTGAGAGCACTTG AAGAGACTCTGGGATCCCATCACCTCAAAGCCTGAGGGTCCCCAAGTCACCGCTGAGAGCACTTG T A ZNF784 Ensembl:ENSG00000179922 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55621133..55621232 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_108860,RMVar_hsa_circ_196348,RMVar_hsa_circ_95286,RMVar_hsa_circ_196347 111270 RMVar_ID_111270 Human_SNP_ID_832388121 m1A Human chr19 + 6767463 6767463 6767463 AAGCTGAGGCTCCGCGGCTCCGGGCTGCTGTCACCCCCGCCCTCCACCTTGCCACCGCCCCAGCC AAGCTGAGGCTCCGCGGCTCCGGGCTGCTGTCCCCCCCGCCCTCCACCTTGCCACCGCCCCAGCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6767354..6767491 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111271 RMVar_ID_111271 Human_SNP_ID_832389249 m1A Human chr19 + 5077456 5077456 5077456 TCATCTCGCCCATCATCCTGAAGAAGTACGGGATCCCCTTCAGCCGGGTGCGTACGGGTGGGGCC TCATCTCGCCCATCATCCTGAAGAAGTACGGGTTCCCCTTCAGCCGGGTGCGTACGGGTGGGGCC A T KDM4B Ensembl:ENSG00000127663 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5077365..5077570 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 8 haematopoietic and lymphoid tissue Human_RBP_ID_910309,Human_RBP_ID_5371099,Human_RBP_ID_8233582,Human_RBP_ID_9381718,Human_RBP_ID_18996125,Human_RBP_ID_22503545 Human_Splice_Rec_1941556,Human_Splice_Rec_1941557,Human_Splice_Rec_1941602,Human_Splice_Rec_1941603,Human_Splice_Rec_1941652,Human_Splice_Rec_1941653,Human_Splice_Rec_1941670,Human_Splice_Rec_1941671,Human_Splice_Rec_1941708,Human_Splice_Rec_1941709,Human_Splice_Rec_1941712,Human_Splice_Rec_1941713 RMVar_hsa_circ_8177,RMVar_hsa_circ_24338,RMVar_hsa_circ_126656,RMVar_hsa_circ_191620,RMVar_hsa_circ_294963,RMVar_hsa_circ_99491,RMVar_hsa_circ_81306,RMVar_hsa_circ_191626,RMVar_hsa_circ_191627,RMVar_hsa_circ_313613,RMVar_hsa_circ_103299,RMVar_hsa_circ_191630,RMVar_hsa_circ_123207,RMVar_hsa_circ_270787,RMVar_hsa_circ_106774,RMVar_hsa_circ_78325,RMVar_hsa_circ_191644,RMVar_hsa_circ_191632,RMVar_hsa_circ_191633,RMVar_hsa_circ_121247,RMVar_hsa_circ_191631,RMVar_hsa_circ_191638,RMVar_hsa_circ_116647,RMVar_hsa_circ_276414,RMVar_hsa_circ_372477,RMVar_hsa_circ_376208,RMVar_hsa_circ_350586,RMVar_hsa_circ_117265,RMVar_hsa_circ_82558,RMVar_hsa_circ_93647,RMVar_hsa_circ_191646,RMVar_hsa_circ_29472,RMVar_hsa_circ_191645,RMVar_hsa_circ_191640,RMVar_hsa_circ_191642,RMVar_hsa_circ_191643,RMVar_hsa_circ_191641,RMVar_hsa_circ_124532,RMVar_hsa_circ_191639,RMVar_hsa_circ_289757,RMVar_hsa_circ_121383,RMVar_hsa_circ_191654,RMVar_hsa_circ_102682,RMVar_hsa_circ_125046,RMVar_hsa_circ_191650,RMVar_hsa_circ_191651,RMVar_hsa_circ_191652,RMVar_hsa_circ_375581,RMVar_hsa_circ_191649,RMVar_hsa_circ_315667,RMVar_hsa_circ_105477,RMVar_hsa_circ_191656,RMVar_hsa_circ_69307,RMVar_hsa_circ_191657,RMVar_hsa_circ_191655,RMVar_hsa_circ_191653 111272 RMVar_ID_111272 Human_SNP_ID_832389349 m1A Human chr19 + 867627 867607 867628 GGGACAGAGTCAGGCAGAGACACAGAAACAGCATGCAGAGACACAGAGACCATACACAGAGAAGT GGGACAGAGTCAG_____________________GCAGAGACACAGAGACCATACACAGAGAAGT GGCAGAGACACAGAAACAGCAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:867373..867801 26863196 MeRIP-seq:(Medium) rs575915108 Functional Loss DEL ICGC 14..34 33 PBCA 1 - 111273 RMVar_ID_111273 Human_SNP_ID_832392180 m1A Human chr19 - 49101466 49101466 49101466 GGGCAGGGCTCGGCGGGAGGTACTCACAGTGCATGTCTCGCTCGTGTTCGTACTCGATGAAGGCA GGGCAGGGCTCGGCGGGAGGTACTCACAGTGCCTGTCTCGCTCGTGTTCGTACTCGATGAAGGCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:49101366..49101543;chr19:49101366..49101531;chr19:49098426..49101538;chr19:49101376..49101475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 111274 RMVar_ID_111274 Human_SNP_ID_832393021 m1A Human chr19 + 45396747 45396747 45396747 GCGCGGCCCAGGAAGTCGAAAGGCGTGGGGGGACCCTGCTGGCGGAGCGGGCCTGGCCCGGGCCG GCGCGGCCCAGGAAGTCGAAAGGCGTGGGGGGGCCCTGCTGGCGGAGCGGGCCTGGCCCGGGCCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45396615..45397070 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111275 RMVar_ID_111275 Human_SNP_ID_832393162 m1A Human chr19 + 50488871 50488871 50488871 AGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACAGAGAGGACAGCGAGAAAAAGAGAACAGGAAGA AGAGCAGAAGTGAGAAAAAGGAGGGTGGCCACTGAGAGGACAGCGAGAAAAAGAGAACAGGAAGA A T EMC10 Ensembl:ENSG00000161671 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:50488595..50488936 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17068565 111276 RMVar_ID_111276 Human_SNP_ID_832396126 m1A Human chr19 - 2811814 2811814 2811814 CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCCATTCAGGACGCCCTCCCTGTCCCCAGTCCCCGC CCTCCCTGTCCCCAGTCCCCGCGTACCTTGCCGTTCAGGACGCCCTCCCTGTCCCCAGTCCCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:2811751..2811875;chr19:2811751..2812016;chr19:2811727..2812001;chr19:2811745..2811875 26863196 MeRIP-seq:(Medium) rs8109048 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 14 prostate,haematopoietic and lymphoid tissue 111277 RMVar_ID_111277 Human_SNP_ID_832399034 m1A Human chr19 + 5903723 5903723 5903723 AAAAACCTTCGGCGCCATAGCCCGCAATCTCGATCCCGCACCACGGACCCCGCCAGCTCGGGAAG AAAAACCTTCGGCGCCATAGCCCGCAATCTCGCTCCCGCACCACGGACCCCGCCAGCTCGGGAAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:5903295..5903787 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 111278 RMVar_ID_111278 Human_SNP_ID_832400628 m1A Human chr19 - 6230623 6230623 6230623 CGCCCGTGAACCACCTGCGCTGCGAGAAGCTCACCTTCAACAACCCCACCACGGAGTTCCGGTAC CGCCCGTGAACCACCTGCGCTGCGAGAAGCTCGCCTTCAACAACCCCACCACGGAGTTCCGGTAC T C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6230495..6230725 26863196 MeRIP-seq:(Medium) rs1470610088 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1019058,Human_RBP_ID_6792810,Human_RBP_ID_9292978,Human_RBP_ID_17271270,Human_RBP_ID_17386178,Human_RBP_ID_17696596,Human_RBP_ID_17933443,Human_RBP_ID_26997177 Human_Splice_Rec_1944320,Human_Splice_Rec_1944321 RMVar_hsa_circ_103247,RMVar_hsa_circ_124471,RMVar_hsa_circ_191792,RMVar_hsa_circ_106203,RMVar_hsa_circ_191794,RMVar_hsa_circ_79495,RMVar_hsa_circ_191793,RMVar_hsa_circ_191795,RMVar_hsa_circ_123437,RMVar_hsa_circ_17517,RMVar_hsa_circ_373252,RMVar_hsa_circ_116392,RMVar_hsa_circ_191799,RMVar_hsa_circ_191797,RMVar_hsa_circ_320665,RMVar_hsa_circ_291229,RMVar_hsa_circ_110627,RMVar_hsa_circ_191800,RMVar_hsa_circ_191802,RMVar_hsa_circ_191803,RMVar_hsa_circ_191801,RMVar_hsa_circ_191804 111279 RMVar_ID_111279 Human_SNP_ID_832404652 m1A Human chr19 + 38817056 38817056 38817056 CACTGCCCAGCTCTAAGCAGGAGCTCGGGAGGATGACTCACCTTCACCTGGAAGAAAGCATCCTG CACTGCCCAGCTCTAAGCAGGAGCTCGGGAGGTTGACTCACCTTCACCTGGAAGAAAGCATCCTG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38817054..38817154 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRC 1 - 111280 RMVar_ID_111280 Human_SNP_ID_832407232 m1A Human chr19 - 806546 806546 806546 CGCGGAGGAAAAGCCCACGTACCTCTGGGTTGAGGTTGCTGACCAGCAATACAGAATTTCCTGCC CGCGGAGGAAAAGCCCACGTACCTCTGGGTTGCGGTTGCTGACCAGCAATACAGAATTTCCTGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:806365..806603 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111281 RMVar_ID_111281 Human_SNP_ID_832408716 m1A Human chr19 - 12650200 12650200 12650200 GTGCCCGCAGACACCCTTGGTGCAGGAGGTGCACCAGAACTTCTCAGCTTGGTGTTCCCAGGTGG GTGCCCGCAGACACCCTTGGTGCAGGAGGTGCGCCAGAACTTCTCAGCTTGGTGTTCCCAGGTGG T C MAN2B1 Ensembl:ENSG00000104774 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12650101..12650200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung mixed_small_cell_carcinoma-adenocarcinoma,lung small_cell_carcinoma 4 lung Human_Splice_Rec_1962232,Human_Splice_Rec_1962233,Human_Splice_Rec_1962284,Human_Splice_Rec_1962285,Human_Splice_Rec_1962326,Human_Splice_Rec_1962327 RMVar_hsa_circ_46947,RMVar_hsa_circ_109163,RMVar_hsa_circ_116609,RMVar_hsa_circ_113679,RMVar_hsa_circ_192702,RMVar_hsa_circ_95806,RMVar_hsa_circ_106184,RMVar_hsa_circ_192703,RMVar_hsa_circ_192704,RMVar_hsa_circ_192700,RMVar_hsa_circ_192701,RMVar_hsa_circ_319035,RMVar_hsa_circ_192706,RMVar_hsa_circ_95049,RMVar_hsa_circ_311520,RMVar_hsa_circ_344180,RMVar_hsa_circ_192707 111282 RMVar_ID_111282 Human_SNP_ID_832412534 m1A Human chr19 + 7500929 7500929 7500929 CTTCTCGCTGGGGCCTGACCTGCGGCTGCACGAGGGCACCATGCGCACCACGTCGCACCGGGACT CTTCTCGCTGGGGCCTGACCTGCGGCTGCACGGGGGCACCATGCGCACCACGTCGCACCGGGACT A G TEX45 Ensembl:ENSG00000198723 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:7500878..7500989 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111283 RMVar_ID_111283 Human_SNP_ID_832412847 m1A Human chr19 - 48469528 48469528 48469528 AACTCCCAGCCGACCCCGCCCCTCCCCGACCTACCATAGACGCCGTCCTCCATGGCGGCTAGGAA AACTCCCAGCCGACCCCGCCCCTCCCCGACCTGCCATAGACGCCGTCCTCCATGGCGGCTAGGAA T C AC008403.2 Ensembl:ENSG00000268530 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48469429..48469687 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_Splice_Rec_2026571 111284 RMVar_ID_111284 Human_SNP_ID_832416273 m1A Human chr19 + 3444136 3444136 3444136 AATACAAAGAGGAGGTCAGATGGGCGTGTGTGACAAATGGCTGCTCCGACGGGGTGATGAGGGCC AATACAAAGAGGAGGTCAGATGGGCGTGTGTGTCAAATGGCTGCTCCGACGGGGTGATGAGGGCC A T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3444133..3444317 26863196 MeRIP-seq:(Medium) rs1160345963 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_17920733 RMVar_hsa_circ_335847,RMVar_hsa_circ_317934,RMVar_hsa_circ_331685,RMVar_hsa_circ_322152,RMVar_hsa_circ_191338,RMVar_hsa_circ_191339,RMVar_hsa_circ_331629,RMVar_hsa_circ_368482 111285 RMVar_ID_111285 Human_SNP_ID_832423719 m1A Human chr19 - 33463043 33463043 33463043 ATACAAATGTCTTTGCTTAATATCCGTCCTCCAGGTAATGAAGGCTGTAAAAGTGGGAATGAAAG ATACAAATGTCTTTGCTTAATATCCGTCCTCCGGGTAATGAAGGCTGTAAAAGTGGGAATGAAAG T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:33462976..33463050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_8483290 Human_Splice_Rec_1990107,Human_Splice_Rec_1990135,Human_Splice_Rec_1990191,Human_Splice_Rec_1990219,Human_Splice_Rec_1990239,Human_Splice_Rec_1990257,Human_Splice_Rec_1990269 RMVar_hsa_circ_114883,RMVar_hsa_circ_194022,RMVar_hsa_circ_194024,RMVar_hsa_circ_353639,RMVar_hsa_circ_374786 111286 RMVar_ID_111286 Human_SNP_ID_832424824 m1A Human chr19 - 11397513 11397513 11397513 GCAGCCCTCGAATCCCCCTCCCGGCGCAGCAGAGCTCGGAGGCCCGTGTCATCCGCGTCAGCATC GCAGCCCTCGAATCCCCCTCCCGGCGCAGCAGTGCTCGGAGGCCCGTGTCATCCGCGTCAGCATC T A RGL3 Ensembl:ENSG00000205517 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:11397394..11397539 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_825458 Human_Splice_Rec_1960342,Human_Splice_Rec_1960343,Human_Splice_Rec_1960380,Human_Splice_Rec_1960381,Human_Splice_Rec_1960404,Human_Splice_Rec_1960405,Human_Splice_Rec_1960440,Human_Splice_Rec_1960441,Human_Splice_Rec_1960445,Human_Splice_Rec_1960482,Human_Splice_Rec_1960483,Human_Splice_Rec_1960487 Human_miRNA_ID_2396206,Human_miRNA_ID_2600176 RMVar_hsa_circ_8935,RMVar_hsa_circ_329168,RMVar_hsa_circ_192592 111287 RMVar_ID_111287 Human_SNP_ID_832425566 m1A Human chr19 - 18388388 18388388 18388388 TCACGTCCCACGACCTTGACGCCGTCGGGGACAGCCGGAACAGAGCCCGGTGAAGGCGGGAGGCC TCACGTCCCACGACCTTGACGCCGTCGGGGACCGCCGGAACAGAGCCCGGTGAAGGCGGGAGGCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18387010..18388729 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 111288 RMVar_ID_111288 Human_SNP_ID_832425991 m1A Human chr19 + 1244360 1244360 1244360 ACTTGGAGAAGGCCCAGGCGGAGCTGGTGGGGACAGCTGACGAGGCCACGCGGGCAGAGATCCAG ACTTGGAGAAGGCCCAGGCGGAGCTGGTGGGGGCAGCTGACGAGGCCACGCGGGCAGAGATCCAG A G ATP5F1D Ensembl:ENSG00000099624 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1244053..1244794;chr19:1244076..1244550;chr19:1244076..1244535 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_513088,Human_RBP_ID_770392,Human_RBP_ID_909983,Human_RBP_ID_4561702,Human_RBP_ID_5115924,Human_RBP_ID_9328034,Human_RBP_ID_17655738,Human_RBP_ID_18995730,Human_RBP_ID_22447115,Human_RBP_ID_22533246,Human_RBP_ID_27463346 Human_Splice_Rec_1931442,Human_Splice_Rec_1931443,Human_Splice_Rec_1931450,Human_Splice_Rec_1931454,Human_Splice_Rec_1931455,Human_Splice_Rec_1931460,Human_Splice_Rec_1931466,Human_Splice_Rec_1931467,Human_Splice_Rec_1931472,Human_Splice_Rec_1931473,Human_Splice_Rec_1931476,Human_Splice_Rec_1931478,Human_Splice_Rec_1931479 RMVar_hsa_circ_108168,RMVar_hsa_circ_85255,RMVar_hsa_circ_191023,RMVar_hsa_circ_102521,RMVar_hsa_circ_191024,RMVar_hsa_circ_191025 111289 RMVar_ID_111289 Human_SNP_ID_832439700 m1A Human chr19 + 34227830 34227828 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG__TGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTA G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1491413946 Functional Loss DEL TCGA 32..33 33 ESCA 1 - Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 111290 RMVar_ID_111290 Human_SNP_ID_832440754 m1A Human chr19 - 47380978 47380978 47380978 AGGAGGGTTCATGCTTACCGTGAGGCAGTTGTAGGTGAGGAAGTCAGTGACTGCGTAGCCCCCCT AGGAGGGTTCATGCTTACCGTGAGGCAGTTGTGGGTGAGGAAGTCAGTGACTGCGTAGCCCCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47380928..47381005 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111291 RMVar_ID_111291 Human_SNP_ID_832441928 m1A Human chr19 + 49497273 49497273 49497273 GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGAAGCTCCCGCGGTACTACAAGAACATCGGTCTGG GAGGGTCCTGCTGGGAGAAACTGGCAAGGAGACGCTCCCGCGGTACTACAAGAACATCGGTCTGG A C RPS11 Ensembl:ENSG00000142534 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49496426..49497375 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate Human_RBP_ID_525368,Human_RBP_ID_1133000,Human_RBP_ID_1569681,Human_RBP_ID_1890935,Human_RBP_ID_3575098,Human_RBP_ID_4571896,Human_RBP_ID_5194270,Human_RBP_ID_5585851,Human_RBP_ID_8256284,Human_RBP_ID_8492049,Human_RBP_ID_9089257,Human_RBP_ID_9381288,Human_RBP_ID_13495622,Human_RBP_ID_17385140,Human_RBP_ID_17502490,Human_RBP_ID_18737484,Human_RBP_ID_22811767,Human_RBP_ID_23131668,Human_RBP_ID_26816188,Human_RBP_ID_26993554 Human_Splice_Rec_2030778,Human_Splice_Rec_2030779,Human_Splice_Rec_2030784,Human_Splice_Rec_2030788,Human_Splice_Rec_2030794,Human_Splice_Rec_2030795,Human_Splice_Rec_2030801,Human_Splice_Rec_2030808,Human_Splice_Rec_2030809,Human_Splice_Rec_2030816,Human_Splice_Rec_2030820,Human_Splice_Rec_2030821,Human_Splice_Rec_2030828,Human_Splice_Rec_2030829 RMVar_hsa_circ_111118,RMVar_hsa_circ_112495,RMVar_hsa_circ_195871,RMVar_hsa_circ_195872,RMVar_hsa_circ_195873,RMVar_hsa_circ_89688 111292 RMVar_ID_111292 Human_SNP_ID_832442539 m1A Human chr19 - 52190176 52190176 52190176 CGCGTCTTCCCCAAGTCCCCCGTAGCCTCCGGACCTGAACGTCCTCATTGCGGAGTTCGTCTATG CGCGTCTTCCCCAAGTCCCCCGTAGCCTCCGGGCCTGAACGTCCTCATTGCGGAGTTCGTCTATG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:52190093..52190191 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 111293 RMVar_ID_111293 Human_SNP_ID_832443390 m1A Human chr19 - 42239998 42239998 42239998 CGTGTACCAGGCACGGCTGGCAGAGACCAGGGAACTAGTCGCCATCAAGAAGGTTCTCCAGGACA CGTGTACCAGGCACGGCTGGCAGAGACCAGGGGACTAGTCGCCATCAAGAAGGTTCTCCAGGACA T C GSK3A,AC006486.1 Ensembl:ENSG00000105723,Ensembl:ENSG00000268643 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42236936..42254986 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_773103 Human_Splice_Rec_2013641,Human_Splice_Rec_2013661,Human_Splice_Rec_2013681,Human_Splice_Rec_2013707 RMVar_hsa_circ_12496,RMVar_hsa_circ_3786,RMVar_hsa_circ_59626,RMVar_hsa_circ_280591,RMVar_hsa_circ_195081,RMVar_hsa_circ_21518 111294 RMVar_ID_111294 Human_SNP_ID_832450508 m1A Human chr19 - 12875709 12875708 12875709 GGTCACATAGCAAGACTCTGTTTCAAAAAAAAAGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT GGTCACATAGCAAGACTCTGTTTCAAAAAAAA_GGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT CT C DNASE2 Ensembl:ENSG00000105612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs113410270 Functional Loss DEL ICGC 33..33 33 BRCA 1 - Human_RBP_ID_5145671,Human_RBP_ID_8198599,Human_RBP_ID_17386683,Human_RBP_ID_26472078 Human_miRNA_ID_1967484 RMVar_hsa_circ_82172,RMVar_hsa_circ_192813 111295 RMVar_ID_111295 Human_SNP_ID_832451472 m1A Human chr19 - 3382076 3382076 3382076 GCGGGATGCCCTTGAACAGGATGACCATGACCAGGTCCAGCCGCCACACCTTGTCCGCCTGCCGG GCGGGATGCCCTTGAACAGGATGACCATGACCGGGTCCAGCCGCCACACCTTGTCCGCCTGCCGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3382051..3382075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111296 RMVar_ID_111296 Human_SNP_ID_832451735 m1A Human chr19 + 13912407 13912407 13912407 CCCGGATGAGGATGAGGAGGAGGGGACGGATGAGGACGACTTGGAGGCTGATGATGACCTGCTGG CCCGGATGAGGATGAGGAGGAGGGGACGGATGGGGACGACTTGGAGGCTGATGATGACCTGCTGG A G CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13912301..13912537 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_5585394,Human_RBP_ID_18994463,Human_RBP_ID_27816170 Human_Splice_Rec_1967352,Human_Splice_Rec_1967353,Human_Splice_Rec_1967426,Human_Splice_Rec_1967427 RMVar_hsa_circ_5050,RMVar_hsa_circ_192940,RMVar_hsa_circ_294116,RMVar_hsa_circ_330538,RMVar_hsa_circ_55614 111297 RMVar_ID_111297 Human_SNP_ID_832455469 m1A Human chr19 + 4043706 4043706 4043706 GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCACCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC GGCGAGGGATGGGGGTCTCCCTGGCCCCCTCCCCCCCCTGGGCCCGGCCCCCCCCCCCCCCCCCC A C HSALNG0123335 RNACentral:URS0000E98386 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:4043696..4043825 26863196 MeRIP-seq:(Medium) rs866300187 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111298 RMVar_ID_111298 Human_SNP_ID_832455750 m1A Human chr19 + 45409233 45409230 45409233 CCTTGAGCCTCAGGCAGCTCCCACATCCACCAAGAAGAAGAAGAAGAAGAAAGAGAGAGGTCACA CCTTGAGCCTCAGGCAGCTCCCACATCCAC___GAAGAAGAAGAAGAAGAAAGAGAGAGGTCACA CCAA C CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45409182..45409282 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 LMS 1 - Human_RBP_ID_53484,Human_RBP_ID_914969,Human_RBP_ID_17936509,Human_RBP_ID_26336413 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 111299 RMVar_ID_111299 Human_SNP_ID_832456249 m1A Human chr19 + 49090474 49090474 49090474 TCCACCTCCCCTTTCTCCTGACAGAGACGGGAAAAGATTGAGCGGCGACAGCAAGAAGTGGAGAC TCCACCTCCCCTTTCTCCTGACAGAGACGGGATAAGATTGAGCGGCGACAGCAAGAAGTGGAGAC A T SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49090236..49090563 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas insulinoma 2 pancreas Human_RBP_ID_52978,Human_RBP_ID_825775,Human_RBP_ID_1191077,Human_RBP_ID_1569533,Human_RBP_ID_1890851,Human_RBP_ID_3955356,Human_RBP_ID_4541745,Human_RBP_ID_5585840,Human_RBP_ID_6778473,Human_RBP_ID_8491837,Human_RBP_ID_9089177,Human_RBP_ID_9381278,Human_RBP_ID_13494102,Human_RBP_ID_18995257,Human_RBP_ID_22594314,Human_RBP_ID_22811641,Human_RBP_ID_22975158,Human_RBP_ID_23114731 Human_Splice_Rec_2028566,Human_Splice_Rec_2028567,Human_Splice_Rec_2028584,Human_Splice_Rec_2028585,Human_Splice_Rec_2028598,Human_Splice_Rec_2028604,Human_Splice_Rec_2028605,Human_Splice_Rec_2028622,Human_Splice_Rec_2028623,Human_Splice_Rec_2028642,Human_Splice_Rec_2028643,Human_Splice_Rec_2028660,Human_Splice_Rec_2028661,Human_Splice_Rec_2028680,Human_Splice_Rec_2028681,Human_Splice_Rec_2028686,Human_Splice_Rec_2028687 RMVar_hsa_circ_369857,RMVar_hsa_circ_195801,RMVar_hsa_circ_299522,RMVar_hsa_circ_369069,RMVar_hsa_circ_195802 111300 RMVar_ID_111300 Human_SNP_ID_832456640 m1A Human chr19 + 47266708 47266708 47266708 GGAGTACCTGCGCTGGAAGCAGGAGAGGGAGAAGATCGACCAGGAGCGGCTGCAGAGGCACCGCA GGAGTACCTGCGCTGGAAGCAGGAGAGGGAGATGATCGACCAGGAGCGGCTGCAGAGGCACCGCA A T CCDC9 Ensembl:ENSG00000105321 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47266659..47270432 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_22977491 Human_Splice_Rec_2023614,Human_Splice_Rec_2023615,Human_Splice_Rec_2023640,Human_Splice_Rec_2023641,Human_Splice_Rec_2023667 RMVar_hsa_circ_76127,RMVar_hsa_circ_355333,RMVar_hsa_circ_195574 111301 RMVar_ID_111301 Human_SNP_ID_832456793 m1A Human chr19 - 14567715 14567715 14567715 TCACTTGCGCAGATGGGAAGGAGCTGGGACCGAGAAAGATGTGGTGGACGTCAGGAGGGCTAGGG TCACTTGCGCAGATGGGAAGGAGCTGGGACCGCGAAAGATGTGGTGGACGTCAGGAGGGCTAGGG T G NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14567713..14568003 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 2 uterus Human_RBP_ID_6722977 111302 RMVar_ID_111302 Human_SNP_ID_832460819 m1A Human chr19 - 46839580 46839580 46839580 AATCTCCGTTGCTGACAGCCTCTCTGTTCTGCAGTTCCGGAACTTTAAGATCATTTACCGCCGCT AATCTCCGTTGCTGACAGCCTCTCTGTTCTGCGGTTCCGGAACTTTAAGATCATTTACCGCCGCT T C AP2S1 Ensembl:ENSG00000042753 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:46839549..46839627;chr19:46839550..46839648 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_18192346,Human_RBP_ID_23802358 Human_Splice_Rec_2023134 RMVar_hsa_circ_124807,RMVar_hsa_circ_195523,RMVar_hsa_circ_114536,RMVar_hsa_circ_118415,RMVar_hsa_circ_195527,RMVar_hsa_circ_195528,RMVar_hsa_circ_195530,RMVar_hsa_circ_293767,RMVar_hsa_circ_195529 111303 RMVar_ID_111303 Human_SNP_ID_832463351 m1A Human chr19 - 48195793 48195793 48195793 TAGCGCCTGGTCCTCCAACTGGGACCCCCTCCAGACATAACCTTCCAGTCCCCAATCTTTCTCAC TAGCGCCTGGTCCTCCAACTGGGACCCCCTCCTGACATAACCTTCCAGTCCCCAATCTTTCTCAC T A CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48195744..48195992 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic 2 skin 111304 RMVar_ID_111304 Human_SNP_ID_832465855 m1A Human chr19 - 52221102 52221102 52221102 CATTGATGCAGAAGAGCGTAGTCATGCGGTGCAGGTAGTTGGGGTCTCCGGACATGGCCAAGACC CATTGATGCAGAAGAGCGTAGTCATGCGGTGCGGGTAGTTGGGGTCTCCGGACATGGCCAAGACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52220952..52221176 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 111305 RMVar_ID_111305 Human_SNP_ID_832465857 m1A Human chr19 - 52221102 52221102 52221102 CATTGATGCAGAAGAGCGTAGTCATGCGGTGCAGGTAGTTGGGGTCTCCGGACATGGCCAAGACC CATTGATGCAGAAGAGCGTAGTCATGCGGTGCCGGTAGTTGGGGTCTCCGGACATGGCCAAGACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52220952..52221176 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 111306 RMVar_ID_111306 Human_SNP_ID_832470552 m1A Human chr19 + 1605408 1605408 1605408 CCCGGTAGCGTGGGCCCAGGAACCGGGTCACCATCGCGGCGGAGTCGCACCCTCAGGATGACCCT CCCGGTAGCGTGGGCCCAGGAACCGGGTCACCGTCGCGGCGGAGTCGCACCCTCAGGATGACCCT A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1605351..1605425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung 111307 RMVar_ID_111307 Human_SNP_ID_832473128 m1A Human chr19 + 13115732 13115732 13115732 CCTTTTCCTCCTCTTGCTCTGACAAGTCCACGACCACTTTTTGCGTGTCCTTCTCTCCTGGAACC CCTTTTCCTCCTCTTGCTCTGACAAGTCCACGGCCACTTTTTGCGTGTCCTTCTCTCCTGGAACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13115608..13115749 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 111308 RMVar_ID_111308 Human_SNP_ID_832473981 m1A Human chr19 - 58380968 58380968 58380968 GACGGCTCCGCGCTGCATGCGGGGCGGGGACCAGGGACCCGTGCGGGCCGCCTCCAGAGAGTAAG GACGGCTCCGCGCTGCATGCGGGGCGGGGACCGGGGACCCGTGCGGGCCGCCTCCAGAGAGTAAG T C ZNF837 Ensembl:ENSG00000152475 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:58380870..58381004 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_8581 Human_Splice_Rec_2051819,Human_Splice_Rec_2051823 111309 RMVar_ID_111309 Human_SNP_ID_832474702 m1A Human chr19 + 11553809 11553809 11553809 CAATCACTGTACACATCCACGGGTTCTGACAGATCTGGGCCACTTAGGTCAAGGGCGATCATTGG CAATCACTGTACACATCCACGGGTTCTGACAGTTCTGGGCCACTTAGGTCAAGGGCGATCATTGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:11553629..11553829 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 10 uterus 111310 RMVar_ID_111310 Human_SNP_ID_832477292 m1A Human chr19 - 14054438 14054438 14054438 GAGGCGAGGAGACCTGGGAGGCAGAGAAGAGAAAAGCGGAAGAATCCATGGGAATAGGAAGTGAG GAGGCGAGGAGACCTGGGAGGCAGAGAAGAGATAAGCGGAAGAATCCATGGGAATAGGAAGTGAG T A PALM3 Ensembl:ENSG00000187867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:14054387..14054558 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_192969,RMVar_hsa_circ_86826 111311 RMVar_ID_111311 Human_SNP_ID_832477461 m1A Human chr19 - 9849123 9849123 9849123 CGGGCCCGCTCATCTCCCCCGTCCGCAGCGCAAACGAGGCGTCTTCAAATGGCTTCTGCATCTGA CGGGCCCGCTCATCTCCCCCGTCCGCAGCGCAGACGAGGCGTCTTCAAATGGCTTCTGCATCTGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:9849101..9849325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 4 uterus 111312 RMVar_ID_111312 Human_SNP_ID_832479587 m1A Human chr19 - 58388230 58388230 58388230 CACCAAGTTCCCCTCACCTGCAGGGAAATGTCATTGATCTGCACATCATCGGTGCTCCACTTCCC CACCAAGTTCCCCTCACCTGCAGGGAAATGTCTTTGATCTGCACATCATCGGTGCTCCACTTCCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58388126..58388295 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111313 RMVar_ID_111313 Human_SNP_ID_832480896 m1A Human chr19 + 45768937 45768937 45768937 TCCTCCCCCACCTGTCCCCCCTTTTCGCCCCCACTCCCCGCTCTTCTCGATCTTCTTTCTGGCCG TCCTCCCCCACCTGTCCCCCCTTTTCGCCCCCCCTCCCCGCTCTTCTCGATCTTCTTTCTGGCCG A C DM1-AS,AC074212.1 Ensembl:ENSG00000267395,Ensembl:ENSG00000259605 lincRNA,lincRNA intron,exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:45768676..45769061 26863196 MeRIP-seq:(Medium) rs1285785204 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_18947092 111314 RMVar_ID_111314 Human_SNP_ID_832481020 m1A Human chr19 - 39398842 39398842 39398842 CCTAGGGTTTCCTTGCAGACGTGGGGTCCAGGACAGGAGGCCATGGAGTGCGAATGTGGGAACCA CCTAGGGTTTCCTTGCAGACGTGGGGTCCAGGCCAGGAGGCCATGGAGTGCGAATGTGGGAACCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39398800..39398901 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111315 RMVar_ID_111315 Human_SNP_ID_832481168 m1A Human chr19 + 40613802 40613802 40613802 CGGTGTTTGCAGGGAGGGAAGTAGCGTGAGGCAGGTTGGGGAAGGCGTGAGAGGCCTAGGAGAGC CGGTGTTTGCAGGGAGGGAAGTAGCGTGAGGCCGGTTGGGGAAGGCGTGAGAGGCCTAGGAGAGC A C LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:40613696..40613893 26863196 MeRIP-seq:(Medium) rs1042376545 Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_8390,Human_RBP_ID_263270,Human_RBP_ID_907789,Human_RBP_ID_3588264,Human_RBP_ID_3955086,Human_RBP_ID_8233155,Human_RBP_ID_9426176,Human_RBP_ID_21979919,Human_RBP_ID_22426374,Human_RBP_ID_26336317,Human_RBP_ID_26783777,Human_RBP_ID_27815454,Human_RBP_ID_27839554 RMVar_hsa_circ_4906 111316 RMVar_ID_111316 Human_SNP_ID_832481265 m1A Human chr19 + 40465692 40465692 40465692 CCGAAGATCGCGATCTTCTTGACGGCCATCGTACGGGATCGTGGGGGTGCAAGGCCTCAGAGTCT CCGAAGATCGCGATCTTCTTGACGGCCATCGTGCGGGATCGTGGGGGTGCAAGGCCTCAGAGTCT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:40465606..40465750;chr19:40465571..40465750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 111317 RMVar_ID_111317 Human_SNP_ID_832484455 m1A Human chr19 - 39840491 39840491 39840491 CTTTATAGGTGGAGGCTTCCATTCTGGTGGCAACCGGGGTCGTGGTCGGGGAGGAAAAAGAGGAA CTTTATAGGTGGAGGCTTCCATTCTGGTGGCATCCGGGGTCGTGGTCGGGGAGGAAAAAGAGGAA T A FBL Ensembl:ENSG00000105202 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T cell line,total RNA;HEK293T,Wild Type chr19:39840304..39846317;chr19:39840303..39840645 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_53141,Human_RBP_ID_521897,Human_RBP_ID_770678,Human_RBP_ID_825600,Human_RBP_ID_907750,Human_RBP_ID_1016112,Human_RBP_ID_3955029,Human_RBP_ID_4568630,Human_RBP_ID_5116884,Human_RBP_ID_5320367,Human_RBP_ID_6762698,Human_RBP_ID_8834185,Human_RBP_ID_8942446,Human_RBP_ID_9087920,Human_RBP_ID_9353597,Human_RBP_ID_17655353,Human_RBP_ID_18441384,Human_RBP_ID_18470727,Human_RBP_ID_18997822,Human_RBP_ID_22071972,Human_RBP_ID_22446751,Human_RBP_ID_22502900,Human_RBP_ID_22531591,Human_RBP_ID_22591893,Human_RBP_ID_22978107,Human_RBP_ID_23797431,Human_RBP_ID_26336289,Human_RBP_ID_26472530 Human_Splice_Rec_2006745,Human_Splice_Rec_2006758,Human_Splice_Rec_2006759,Human_Splice_Rec_2006780,Human_Splice_Rec_2006781,Human_Splice_Rec_2006793,Human_Splice_Rec_2006805,Human_Splice_Rec_2006817,Human_Splice_Rec_2006828,Human_Splice_Rec_2006829,Human_Splice_Rec_2006838,Human_Splice_Rec_2006839,Human_Splice_Rec_2006846,Human_Splice_Rec_2006847,Human_Splice_Rec_2006854,Human_Splice_Rec_2006855 RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_30690,RMVar_hsa_circ_352928,RMVar_hsa_circ_194797,RMVar_hsa_circ_194801,RMVar_hsa_circ_375114,RMVar_hsa_circ_194802,RMVar_hsa_circ_376972 111318 RMVar_ID_111318 Human_SNP_ID_832485446 m1A Human chr19 + 48873951 48873951 48873951 ATCAAGCCACGGAGGATAAAAGAACAGAAAGAAGTAAAGGAGCCAGGAAGACCTCCGTGTCCCCC ATCAAGCCACGGAGGATAAAAGAACAGAAAGAGGTAAAGGAGCCAGGAAGACCTCCGTGTCCCCC A G PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48873576..48874810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney Human_RBP_ID_52796,Human_RBP_ID_1569445,Human_RBP_ID_4541270,Human_RBP_ID_5145358,Human_RBP_ID_8491721,Human_RBP_ID_26338091,Human_RBP_ID_26472782,Human_RBP_ID_27815560 RMVar_hsa_circ_89556,RMVar_hsa_circ_195728 111319 RMVar_ID_111319 Human_SNP_ID_832488237 m1A Human chr19 + 57487814 57487814 57487814 CTGCGAGAAGCTGGTTGTGCGCTGAGGCGACCAGCGCCGGAAGGCACGGTGGCGACTCACGCTGT CTGCGAGAAGCTGGTTGTGCGCTGAGGCGACCGGCGCCGGAAGGCACGGTGGCGACTCACGCTGT A G ZNF419,AC003005.1 Ensembl:ENSG00000105136,Ensembl:ENSG00000268107 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:57487763..57487946 26863196 MeRIP-seq:(Medium) rs8113039 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_18740467 111320 RMVar_ID_111320 Human_SNP_ID_832494404 m1A Human chr19 + 35784602 35784602 35784602 TGGGGCCATGGGTCCACCTGGGAGGAGGTGGGAGGTCCCCAGACTTGACCCCGCCCCGGCCCCAC TGGGGCCATGGGTCCACCTGGGAGGAGGTGGGGGGTCCCCAGACTTGACCCCGCCCCGGCCCCAC A G ARHGAP33 Ensembl:ENSG00000004777 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35784511..35784623 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_909562 111321 RMVar_ID_111321 Human_SNP_ID_832498365 m1A Human chr19 - 49557245 49557245 49557245 GATGCTCAGCCCACTTTCCCCGACGCAGGCCTACGAGAAGCAGCGGGGCACCCGGCGCGAGGAGC GATGCTCAGCCCACTTTCCCCGACGCAGGCCTGCGAGAAGCAGCGGGGCACCCGGCGCGAGGAGC T C NOSIP Ensembl:ENSG00000142546 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49557101..49557291 26863196 MeRIP-seq:(Medium) rs1367188779 Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_826515,Human_RBP_ID_4542290,Human_RBP_ID_9381300,Human_RBP_ID_19094002,Human_RBP_ID_22070436,Human_RBP_ID_26338141,Human_RBP_ID_27815588 Human_Splice_Rec_2030988,Human_Splice_Rec_2031002,Human_Splice_Rec_2031030,Human_Splice_Rec_2031062,Human_Splice_Rec_2031076,Human_Splice_Rec_2031086,Human_Splice_Rec_2031098,Human_Splice_Rec_2031120 RMVar_hsa_circ_195879,RMVar_hsa_circ_79136,RMVar_hsa_circ_109332,RMVar_hsa_circ_195880 111322 RMVar_ID_111322 Human_SNP_ID_832500745 m1A Human chr19 - 58517060 58517060 58517060 TGCTGACCCCTCACTGTCCGCGGCCCCTGATGACCGAGGTGACGAGGATGACGAGGAAAGTGACG TGCTGACCCCTCACTGTCCGCGGCCCCTGATGTCCGAGGTGACGAGGATGACGAGGAAAGTGACG T A ZBTB45 Ensembl:ENSG00000119574 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58517010..58517326 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium serous_carcinoma 3 uterus 111323 RMVar_ID_111323 Human_SNP_ID_832515869 m1A Human chr19 - 10115811 10115809 10115812 GCCACCTCCCCTCTCCCACACAGCCGACGACAACGCCACCATCCGTGTCACCAACTTGTCAGAGG GCCACCTCCCCTCTCCCACACAGCCGACGAC___GCCACCATCCGTGTCACCAACTTGTCAGAGG CGTT C EIF3G Ensembl:ENSG00000130811 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:10115667..10115852;chr19:10115804..10115930 26863196 MeRIP-seq:(Medium) rs758688972 Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_240288,Human_RBP_ID_5421096,Human_RBP_ID_18192850,Human_RBP_ID_26815217 Human_Splice_Rec_1953282,Human_Splice_Rec_1953296,Human_Splice_Rec_1953314,Human_Splice_Rec_1953330,Human_Splice_Rec_1953346 Human_miRNA_ID_1957681 RMVar_hsa_circ_102942,RMVar_hsa_circ_124534,RMVar_hsa_circ_192266,RMVar_hsa_circ_87997,RMVar_hsa_circ_192267,RMVar_hsa_circ_192265,RMVar_hsa_circ_192268 111324 RMVar_ID_111324 Human_SNP_ID_832516162 m1A Human chr19 + 1407584 1407584 1407584 GTGCGCAGGGGCGGCGGCGCGGCGGCGCGGGGACGCGCGGTGACCGTTGGCGCCGAGGGGAGGAG GTGCGCAGGGGCGGCGGCGCGGCGGCGCGGGGGCGCGCGGTGACCGTTGGCGCCGAGGGGAGGAG A G DAZAP1 Ensembl:ENSG00000071626 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:1407576..1407858;chr19:1407576..1407826 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4504401 RMVar_hsa_circ_101096,RMVar_hsa_circ_191053 111325 RMVar_ID_111325 Human_SNP_ID_832518516 m1A Human chr19 + 48121276 48121276 48121276 GCTTCCCCCGGCCCAGGTAGGCGCCGATCACCACCAGGTCCAGGGTGTCACCCACGCCATCAAGG GCTTCCCCCGGCCCAGGTAGGCGCCGATCACCGCCAGGTCCAGGGTGTCACCCACGCCATCAAGG A G AC011466.3 Ensembl:ENSG00000269534 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48121226..48121356 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 111326 RMVar_ID_111326 Human_SNP_ID_832521093 m1A Human chr19 - 10259777 10259777 10259777 CAGTGGTACGGGGTGGCCGCTGGGCCCTGGGTAGCGTGGGGTAGGGGTCGGGGGAAGTCGCTGTA CAGTGGTACGGGGTGGCCGCTGGGCCCTGGGTGGCGTGGGGTAGGGGTCGGGGGAAGTCGCTGTA T C AC011511.2,AC011511.3 Ensembl:ENSG00000266978,Ensembl:ENSG00000267105 lincRNA,lincRNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:10259626..10259946;chr19:10259726..10259875 26863196 MeRIP-seq:(Medium) rs1195546337 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 111327 RMVar_ID_111327 Human_SNP_ID_832522486 m1A Human chr19 + 39342743 39342743 39342743 TGCGGAACGCGGGCCTCGGGGGGCCGGGCCCCACGGGAGAAGCCCCGCGCCCGTCCCCAGTCTCC TGCGGAACGCGGGCCTCGGGGGGCCGGGCCCCCCGGGAGAAGCCCCGCGCCCGTCCCCAGTCTCC A C SAMD4B Ensembl:ENSG00000179134 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:39342735..39342809;chr19:39342734..39342839 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5373863,Human_RBP_ID_9425325,Human_RBP_ID_17657053,Human_RBP_ID_22234800,Human_RBP_ID_22546015,Human_RBP_ID_26783768 111328 RMVar_ID_111328 Human_SNP_ID_832527031 m1A Human chr19 + 12943783 12943783 12943783 GCAGAGGCTTAAGGAGGAGGAAGAAGACAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGACAAGG GCAGAGGCTTAAGGAGGAGGAAGAAGACAAGAGACGCAAAGAGGAGGAGGAGGCAGAGGACAAGG A G CALR Ensembl:ENSG00000179218 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:12943526..12944084;chr19:12943551..12944351 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue essential_thrombocythaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_825947,Human_RBP_ID_2556494,Human_RBP_ID_5116727,Human_RBP_ID_5585366,Human_RBP_ID_6721337,Human_RBP_ID_9380617,Human_RBP_ID_13372465,Human_RBP_ID_22391076,Human_RBP_ID_22966984,Human_RBP_ID_23783075,Human_RBP_ID_24545579,Human_RBP_ID_24552816,Human_RBP_ID_26335808,Human_RBP_ID_26983149,Human_RBP_ID_27463687,Human_RBP_ID_27815187 Human_Splice_Rec_1964392,Human_Splice_Rec_1964416,Human_Splice_Rec_1964418 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_110485,RMVar_hsa_circ_192843,RMVar_hsa_circ_192844,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_81328,RMVar_hsa_circ_192849,RMVar_hsa_circ_192851,RMVar_hsa_circ_76392,RMVar_hsa_circ_192853,RMVar_hsa_circ_192854,RMVar_hsa_circ_110866,RMVar_hsa_circ_192855,RMVar_hsa_circ_378042 111329 RMVar_ID_111329 Human_SNP_ID_832536535 m1A Human chr19 - 4064823 4064823 4064823 ATGCAGCCAGGAGTTGGCGGCGAGGCGGGGGGAGGCAGCAACTCCTCTCCCCCCAGTCAGGCGGC ATGCAGCCAGGAGTTGGCGGCGAGGCGGGGGGGGGCAGCAACTCCTCTCCCCCCAGTCAGGCGGC T C ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4064822..4065005 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3580550,Human_RBP_ID_8195805,Human_RBP_ID_8728028,Human_RBP_ID_22719866 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 111330 RMVar_ID_111330 Human_SNP_ID_832537087 m1A Human chr19 - 3366564 3366564 3366564 GCGCTGAACTTACTGAGTCATTTTTCCAAACCACCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC GCGCTGAACTTACTGAGTCATTTTTCCAAACCCCCCCCCCGCCCCCCCCAACCCCCCCCCCCGCC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:3366526..3366575;chr19:3366551..3366806 26863196 MeRIP-seq:(Medium) rs866086214 Functional Loss SNV ICGC 33..33 33 STAD 1 - 111331 RMVar_ID_111331 Human_SNP_ID_832537218 m1A Human chr19 - 45730862 45730862 45730862 GTGGGGGAAACCCGCGTAGCCGAGGGAGATGCAGCGCGCGGCGATGGTGAGAGCCCAGGCGCGGG GTGGGGGAAACCCGCGTAGCCGAGGGAGATGCCGCGCGCGGCGATGGTGAGAGCCCAGGCGCGGG T G FBXO46 Ensembl:ENSG00000177051 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:45730665..45730900;chr19:45730139..45730900;chr19:45730186..45730900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_Splice_Rec_2020583 111332 RMVar_ID_111332 Human_SNP_ID_832538954 m1A Human chr19 + 11417004 11417004 11417004 CCACCAGCCGCTCCAGGCGCGCTGCCCTCAGCACCCTCACCTTGCTGGTTCGATAGTGGAGGAAG CCACCAGCCGCTCCAGGCGCGCTGCCCTCAGCCCCCTCACCTTGCTGGTTCGATAGTGGAGGAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11416792..11417061 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111333 RMVar_ID_111333 Human_SNP_ID_832541607 m1A Human chr19 - 18279927 18279927 18279927 GTTGGTTTTTTAAAGAAATGGGAAGAAGAAAAAAAAATTCTCCGCCCCTTTCCTCGATCTCGCTC GTTGGTTTTTTAAAGAAATGGGAAGAAGAAAACAAAATTCTCCGCCCCTTTCCTCGATCTCGCTC T G JUND Ensembl:ENSG00000130522 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18279876..18280000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_516083,Human_RBP_ID_1556442,Human_RBP_ID_1881168,Human_RBP_ID_2559128,Human_RBP_ID_3564531,Human_RBP_ID_8948205,Human_RBP_ID_18945223,Human_RBP_ID_22978529,Human_RBP_ID_23786500 111334 RMVar_ID_111334 Human_SNP_ID_832543133 m1A Human chr19 + 9621174 9621174 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGCCGACTCCACCACCATAAAGGCGAAACCGCACTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs10401707 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,ESCA 4 ovary GWAS_ID_9603,GWAS_ID_9604,GWAS_ID_9605 111335 RMVar_ID_111335 Human_SNP_ID_832543134 m1A Human chr19 + 9621174 9621174 9621174 GCCAAGGAGGTGGAACTCACCACAGCCTGGGCAGACTCCACCACCATAAAGGCGAAACCGCACTG GCCAAGGAGGTGGAACTCACCACAGCCTGGGCGGACTCCACCACCATAAAGGCGAAACCGCACTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:9621007..9621173 26863196 MeRIP-seq:(Medium) rs10401707 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_9603,GWAS_ID_9604,GWAS_ID_9605 111336 RMVar_ID_111336 Human_SNP_ID_832544633 m1A Human chr19 - 17273999 17273999 17273999 GCCTCACCCAGGCCGTGTCATCGTTCACCACCACCAGTGCAAACTCGTGGCTTTTGTCGATCTTG GCCTCACCCAGGCCGTGTCATCGTTCACCACCCCCAGTGCAAACTCGTGGCTTTTGTCGATCTTG T G USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:17273951..17274282 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 111337 RMVar_ID_111337 Human_SNP_ID_832545705 m1A Human chr19 + 38840222 38840222 38840222 TCGGCGTGAGGGCCATACTCGGGTGGTGGGGGAGGGGGTGGGGGGTGCCCATACTGGGGGCCGTA TCGGCGTGAGGGCCATACTCGGGTGGTGGGGGGGGGGGTGGGGGGTGCCCATACTGGGGGCCGTA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:38840201..38840225;chr19:38840176..38840225 26863196 MeRIP-seq:(Medium) rs747010552 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,thyroid neoplasm,haematopoietic_and_lymphoid_tissue chronic_myelomonocytic_leukaemia,head_neck squamous_cell_carcinoma,CHOL 17 lung,head and neck,haematopoietic and lymphoid tissue 111338 RMVar_ID_111338 Human_SNP_ID_832547283 m1A Human chr19 - 38836537 38836537 38836537 CCTTAATGGAAACGCTGGAAATCTGCAGGGGGAGGGAGAGGGGAACTGTTATCTCCCAAGATTAA CCTTAATGGAAACGCTGGAAATCTGCAGGGGGGGGGAGAGGGGAACTGTTATCTCCCAAGATTAA T C AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding intron,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:38836487..38836587 32194978 MeRIP-seq:(Medium) rs1478060173 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_239442,Human_RBP_ID_521222,Human_RBP_ID_770490,Human_RBP_ID_1564180,Human_RBP_ID_1887094,Human_RBP_ID_2565145,Human_RBP_ID_3571344,Human_RBP_ID_5116243,Human_RBP_ID_5145200,Human_RBP_ID_6759944,Human_RBP_ID_8486665,Human_RBP_ID_13450505,Human_RBP_ID_17068332,Human_RBP_ID_17657040,Human_RBP_ID_18731793,Human_RBP_ID_20349376,Human_RBP_ID_22810664,Human_RBP_ID_22971860,Human_RBP_ID_23131148,Human_RBP_ID_23210950,Human_RBP_ID_23796500,Human_RBP_ID_24420049,Human_RBP_ID_24484315,Human_RBP_ID_26474905 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_194675 111339 RMVar_ID_111339 Human_SNP_ID_832548211 m1A Human chr19 + 49461291 49461291 49461291 GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGACCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT GGACTCCTGGGTCTGAGGGAGGAGGGGCTGGGGCCTGGACTCCTGGGTCTGAGGGAGGAGGGGCT A G ALDH16A1 Ensembl:ENSG00000161618 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:49461284..49461427;chr19:49461276..49461451 26863196 MeRIP-seq:(Medium) rs559858125 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_263338,Human_RBP_ID_826988,Human_RBP_ID_3583940,Human_RBP_ID_3955386,Human_RBP_ID_5321832,Human_RBP_ID_8100778,Human_RBP_ID_8196785,Human_RBP_ID_8233206,Human_RBP_ID_8942486,Human_RBP_ID_9426363,Human_RBP_ID_17190782,Human_RBP_ID_21979375 RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 111340 RMVar_ID_111340 Human_SNP_ID_832549461 m1A Human chr19 - 14120593 14120593 14120593 GCTTCCATATCAACTGGGACAACAACATGGACAGGCTGGAGGCCATAGAGACCCAGGACCCCTCC GCTTCCATATCAACTGGGACAACAACATGGACGGGCTGGAGGCCATAGAGACCCAGGACCCCTCC T C ASF1B Ensembl:ENSG00000105011 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_1013285,Human_RBP_ID_1555288,Human_RBP_ID_17266797,Human_RBP_ID_17382194,Human_RBP_ID_26817130 Human_Splice_Rec_1968082,Human_Splice_Rec_1968086,Human_Splice_Rec_1968092,Human_Splice_Rec_1968096 Human_miRNA_ID_2225817,Human_miRNA_ID_2974964,Human_miRNA_ID_3008160 RMVar_hsa_circ_92962,RMVar_hsa_circ_112658,RMVar_hsa_circ_95845,RMVar_hsa_circ_192976,RMVar_hsa_circ_192977,RMVar_hsa_circ_192975 111341 RMVar_ID_111341 Human_SNP_ID_832551835 m1A Human chr19 + 12922791 12922791 12922791 CCTGTGTGGGAGGGGGCCTCGGCTCGGCATCCAGGCGGCACAGGGGACTGTCATACACCATCTGC CCTGTGTGGGAGGGGGCCTCGGCTCGGCATCCGGGCGGCACAGGGGACTGTCATACACCATCTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12922746..12922919 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111342 RMVar_ID_111342 Human_SNP_ID_832560947 m1A Human chr19 + 55112681 55112681 55112681 CCCTCCCTTGCCTCACCTGGCGATATCTAGGTAGCCACAGGAGGCGGCCACGTGCAGTGGCGTCC CCCTCCCTTGCCTCACCTGGCGATATCTAGGTGGCCACAGGAGGCGGCCACGTGCAGTGGCGTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55112463..55112863 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 111343 RMVar_ID_111343 Human_SNP_ID_832562085 m1A Human chr19 + 892684 892654 892685 TCCCTCTCCAGGCCCCGCACCGATAACCCCGCAGTCTCCAGGCCCTGCCTCTACAGCCCCCCAGT TCC_______________________________TCTCCAGGCCCTGCCTCTACAGCCCCCCAGT CCTCTCCAGGCCCCGCACCGATAACCCCGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:892653..892965 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 4..34 33 SKCA 1 - 111344 RMVar_ID_111344 Human_SNP_ID_832565056 m1A Human chr19 + 44909194 44909194 44909194 ACATGCAGCGCCAGTGGGCCGGGCTGGTGGAGAAGGTGCAGGCTGCCGTGGGCACCAGCGCCGCC ACATGCAGCGCCAGTGGGCCGGGCTGGTGGAGTAGGTGCAGGCTGCCGTGGGCACCAGCGCCGCC A T APOE Ensembl:ENSG00000130203 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:44909093..44909194 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_914731,Human_RBP_ID_5117528,Human_RBP_ID_5145788,Human_RBP_ID_8840127,Human_RBP_ID_9293801,Human_RBP_ID_17656212,Human_RBP_ID_17935011,Human_RBP_ID_18735608,Human_RBP_ID_22447852,Human_RBP_ID_22763032 Human_miRNA_ID_2751249 RMVar_hsa_circ_80434,RMVar_hsa_circ_83394,RMVar_hsa_circ_195253,RMVar_hsa_circ_195254 111345 RMVar_ID_111345 Human_SNP_ID_832567903 m1A Human chr19 - 4065003 4065003 4065003 GGAGCCTGGCTGGGGGCTGAGCGGAGCGGAGGAGCGGGTGCCCCCCCAGGGACCGGGCCTCTGCG GGAGCCTGGCTGGGGGCTGAGCGGAGCGGAGGTGCGGGTGCCCCCCCAGGGACCGGGCCTCTGCG T A ZBTB7A Ensembl:ENSG00000178951 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:4064989..4065134 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_5375190,Human_RBP_ID_8195808,Human_RBP_ID_9426904,Human_RBP_ID_18461742 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 111346 RMVar_ID_111346 Human_SNP_ID_832569893 m1A Human chr19 - 49130528 49130528 49130528 TGCCTTGCCCAGCTCACGGTGCGCGGTGCCCAACTCCTCCTCCAGCTGGCTCATCTGACGGCACA TGCCTTGCCCAGCTCACGGTGCGCGGTGCCCAGCTCCTCCTCCAGCTGGCTCATCTGACGGCACA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49130401..49130575 26863196 MeRIP-seq:(Medium) rs780338052 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 111347 RMVar_ID_111347 Human_SNP_ID_832570320 m1A Human chr19 + 10921126 10921126 10921126 TCCAGCGTGGGCCACAACAACCTGATTCCTTTAGGTGAGTGTCCCCCAGGGCCAGGGGCAGCAGG TCCAGCGTGGGCCACAACAACCTGATTCCTTTTGGTGAGTGTCCCCCAGGGCCAGGGGCAGCAGG A T CARM1 Ensembl:ENSG00000142453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10921090..10921437 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 2 lung Human_RBP_ID_17387225,Human_RBP_ID_19089273,Human_RBP_ID_27561937 Human_Splice_Rec_1956594,Human_Splice_Rec_1956595,Human_Splice_Rec_1956628,Human_Splice_Rec_1956629,Human_Splice_Rec_1956656,Human_Splice_Rec_1956657,Human_Splice_Rec_1956684,Human_Splice_Rec_1956685,Human_Splice_Rec_1956724,Human_Splice_Rec_1956725,Human_Splice_Rec_1956731 RMVar_hsa_circ_10779,RMVar_hsa_circ_347974,RMVar_hsa_circ_192456,RMVar_hsa_circ_40682,RMVar_hsa_circ_192470,RMVar_hsa_circ_83729,RMVar_hsa_circ_315594 111348 RMVar_ID_111348 Human_SNP_ID_832576056 m1A Human chr19 + 1012532 1012532 1012532 GCGGGTGGCCTGCGACAGGCGAAGGAAGCCATACTCTAGTGAGTACTCCACGATGTACTCGTCCT GCGGGTGGCCTGCGACAGGCGAAGGAAGCCATTCTCTAGTGAGTACTCCACGATGTACTCGTCCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1012460..1012575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 111349 RMVar_ID_111349 Human_SNP_ID_832576134 m1A Human chr19 + 33204704 33204685 33204704 TGCTCCCTGGACTGGCTCCTGCTGGGCCCAGCAGCCCCACCCCGCCAGGAGGCCTTCCGCCTCTG TGCTCCCTGGACTG___________________GCCCCACCCCGCCAGGAGGCCTTCCGCCTCTG GGCTCCTGCTGGGCCCAGCA G LRP3 Ensembl:ENSG00000130881 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:33204620..33204779 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 15..33 33 ESCA 1 - Human_RBP_ID_18997420,Human_RBP_ID_27466790 Human_Splice_Rec_1989980,Human_Splice_Rec_1989988,Human_Splice_Rec_1989998 111350 RMVar_ID_111350 Human_SNP_ID_832584061 m1A Human chr19 - 48902699 48902699 48902699 TTGACTTAACATATCTCTCCAGTTCAGAACTCAGTGGCTCACACCTATTATCCCAGCACTTTGGG TTGACTTAACATATCTCTCCAGTTCAGAACTCGGTGGCTCACACCTATTATCCCAGCACTTTGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48902695..48902860 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111351 RMVar_ID_111351 Human_SNP_ID_832587749 m1A Human chr19 + 50413520 50413520 50413520 CACAGTGGAGAATGGCTACAGCACCAGTGCCAAGGTCGGGGGCTGCCCACCGCTGCCCTGAGATG CACAGTGGAGAATGGCTACAGCACCAGTGCCAGGGTCGGGGGCTGCCCACCGCTGCCCTGAGATG A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50413484..50413568 26863196 MeRIP-seq:(Medium) rs771176744 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 4 kidney Human_RBP_ID_3955487,Human_RBP_ID_19094143 Human_Splice_Rec_2035480,Human_Splice_Rec_2035481,Human_Splice_Rec_2035530,Human_Splice_Rec_2035531,Human_Splice_Rec_2035582,Human_Splice_Rec_2035583,Human_Splice_Rec_2035636,Human_Splice_Rec_2035637,Human_Splice_Rec_2035692,Human_Splice_Rec_2035693,Human_Splice_Rec_2035736,Human_Splice_Rec_2035737,Human_Splice_Rec_2035788,Human_Splice_Rec_2035789,Human_Splice_Rec_2035844,Human_Splice_Rec_2035845,Human_Splice_Rec_2035849 RMVar_hsa_circ_100166,RMVar_hsa_circ_195997,RMVar_hsa_circ_46238,RMVar_hsa_circ_75880,RMVar_hsa_circ_195999,RMVar_hsa_circ_122704,RMVar_hsa_circ_196001 111352 RMVar_ID_111352 Human_SNP_ID_832588915 m1A Human chr19 + 55347451 55347451 55347451 CGACCTGGATGTCGGCGGTGAAGAGCTGTGACAGGCCGGACGGGGAGGCCCAGCAGGGAGAGAGG CGACCTGGATGTCGGCGGTGAAGAGCTGTGACTGGCCGGACGGGGAGGCCCAGCAGGGAGAGAGG A T KMT5C Ensembl:ENSG00000133247 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55347401..55347469 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_93230,RMVar_hsa_circ_196324 111353 RMVar_ID_111353 Human_SNP_ID_832590714 m1A Human chr19 + 35158378 35158378 35158378 GCAGTCTACACAGAACTCCAGCCCACCTCTCCAACCCCAACCTGGCCTGCTGATGGTGAGTAGTG GCAGTCTACACAGAACTCCAGCCCACCTCTCCGACCCCAACCTGGCCTGCTGATGGTGAGTAGTG A G FXYD5 Ensembl:ENSG00000089327 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:35157365..35159546;chr19:35155483..35159546 26863196 MeRIP-seq:(Medium) rs1128882 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_770258,Human_RBP_ID_17268023,Human_RBP_ID_17386794,Human_RBP_ID_18728925,Human_RBP_ID_26817396 Human_Splice_Rec_1992614,Human_Splice_Rec_1992615,Human_Splice_Rec_1992622,Human_Splice_Rec_1992623,Human_Splice_Rec_1992636,Human_Splice_Rec_1992637,Human_Splice_Rec_1992652,Human_Splice_Rec_1992653,Human_Splice_Rec_1992668,Human_Splice_Rec_1992669,Human_Splice_Rec_1992684,Human_Splice_Rec_1992685,Human_Splice_Rec_1992702,Human_Splice_Rec_1992703,Human_Splice_Rec_1992716,Human_Splice_Rec_1992717,Human_Splice_Rec_1992732,Human_Splice_Rec_1992733,Human_Splice_Rec_1992748,Human_Splice_Rec_1992749 Human_miRNA_ID_2223908,Human_miRNA_ID_2223909,Human_miRNA_ID_2486978,Human_miRNA_ID_2486979,Human_miRNA_ID_3075343,Human_miRNA_ID_3075344 RMVar_hsa_circ_77352,RMVar_hsa_circ_122291,RMVar_hsa_circ_105676,RMVar_hsa_circ_194214,RMVar_hsa_circ_194215,RMVar_hsa_circ_194216 111354 RMVar_ID_111354 Human_SNP_ID_832591448 m1A Human chr19 - 1440408 1440408 1440408 GAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCATGCTTTACGGGCTTGTAGGTGATGGAGAACTC GAGGAGTGGGTGGCCCCGATGCCGGGCCGGCCGTGCTTTACGGGCTTGTAGGTGATGGAGAACTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEK293T,Wild Type;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:1440362..1440456;chr19:1440220..1440500;chr19:1440376..1440475;chr19:1440361..1440450;chr19:1440344..1440475 26863196,26863410,26863196,26863196,32194978,32194978 MeRIP-seq:(Medium) rs767434466 Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 10 uterus 111355 RMVar_ID_111355 Human_SNP_ID_832593142 m1A Human chr19 + 1220450 1220450 1220450 GGGCATTGTGCACAAGGACATCAAGCCGGGGAACCTGCTGCTCACCACCGGTGGCACCCTCAAAA GGGCATTGTGCACAAGGACATCAAGCCGGGGAGCCTGCTGCTCACCACCGGTGGCACCCTCAAAA A G STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1220401..1220500 32194978 MeRIP-seq:(Medium) rs886037859 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma,lung adenocarcinoma 4 lung,biliary tract,gallbladder Human_RBP_ID_906931,Human_RBP_ID_1554255,Human_RBP_ID_1879949,Human_RBP_ID_6719374,Human_RBP_ID_9329341 Human_Splice_Rec_1931252,Human_Splice_Rec_1931253,Human_Splice_Rec_1931268,Human_Splice_Rec_1931269,Human_Splice_Rec_1931284,Human_Splice_Rec_1931285,Human_Splice_Rec_1931302,Human_Splice_Rec_1931303,Human_Splice_Rec_1931312,Human_Splice_Rec_1931313,Human_Splice_Rec_1931318 Human_miRNA_ID_599651,Human_miRNA_ID_1240306,Human_miRNA_ID_2102265,Human_miRNA_ID_2108220,Human_miRNA_ID_2114160,Human_miRNA_ID_2166704,Human_miRNA_ID_2223691,Human_miRNA_ID_2486763,Human_miRNA_ID_2597962,Human_miRNA_ID_2740868,Human_miRNA_ID_3041454,Human_miRNA_ID_3075126 Clinvar_Rec_371 RMVar_hsa_circ_77058,RMVar_hsa_circ_26746,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017 111356 RMVar_ID_111356 Human_SNP_ID_832593144 m1A Human chr19 + 1220450 1220450 1220450 GGGCATTGTGCACAAGGACATCAAGCCGGGGAACCTGCTGCTCACCACCGGTGGCACCCTCAAAA GGGCATTGTGCACAAGGACATCAAGCCGGGGACCCTGCTGCTCACCACCGGTGGCACCCTCAAAA A C STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1220401..1220500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_906931,Human_RBP_ID_1554255,Human_RBP_ID_1879949,Human_RBP_ID_6719374,Human_RBP_ID_9329341 Human_Splice_Rec_1931252,Human_Splice_Rec_1931253,Human_Splice_Rec_1931268,Human_Splice_Rec_1931269,Human_Splice_Rec_1931284,Human_Splice_Rec_1931285,Human_Splice_Rec_1931302,Human_Splice_Rec_1931303,Human_Splice_Rec_1931312,Human_Splice_Rec_1931313,Human_Splice_Rec_1931318 Human_miRNA_ID_599651,Human_miRNA_ID_1240306,Human_miRNA_ID_2102265,Human_miRNA_ID_2108220,Human_miRNA_ID_2114160,Human_miRNA_ID_2166704,Human_miRNA_ID_2223691,Human_miRNA_ID_2486763,Human_miRNA_ID_2597962,Human_miRNA_ID_2740868,Human_miRNA_ID_3041454,Human_miRNA_ID_3075126 RMVar_hsa_circ_77058,RMVar_hsa_circ_26746,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017 111357 RMVar_ID_111357 Human_SNP_ID_832593149 m1A Human chr19 + 1220450 1220450 1220450 GGGCATTGTGCACAAGGACATCAAGCCGGGGAACCTGCTGCTCACCACCGGTGGCACCCTCAAAA GGGCATTGTGCACAAGGACATCAAGCCGGGGATCCTGCTGCTCACCACCGGTGGCACCCTCAAAA A T STK11 Ensembl:ENSG00000118046 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1220401..1220500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_906931,Human_RBP_ID_1554255,Human_RBP_ID_1879949,Human_RBP_ID_6719374,Human_RBP_ID_9329341 Human_Splice_Rec_1931252,Human_Splice_Rec_1931253,Human_Splice_Rec_1931268,Human_Splice_Rec_1931269,Human_Splice_Rec_1931284,Human_Splice_Rec_1931285,Human_Splice_Rec_1931302,Human_Splice_Rec_1931303,Human_Splice_Rec_1931312,Human_Splice_Rec_1931313,Human_Splice_Rec_1931318 Human_miRNA_ID_599651,Human_miRNA_ID_1240306,Human_miRNA_ID_2102265,Human_miRNA_ID_2108220,Human_miRNA_ID_2114160,Human_miRNA_ID_2166704,Human_miRNA_ID_2223691,Human_miRNA_ID_2486763,Human_miRNA_ID_2597962,Human_miRNA_ID_2740868,Human_miRNA_ID_3041454,Human_miRNA_ID_3075126 RMVar_hsa_circ_77058,RMVar_hsa_circ_26746,RMVar_hsa_circ_333282,RMVar_hsa_circ_328917,RMVar_hsa_circ_48030,RMVar_hsa_circ_191013,RMVar_hsa_circ_80952,RMVar_hsa_circ_113229,RMVar_hsa_circ_191014,RMVar_hsa_circ_79244,RMVar_hsa_circ_191015,RMVar_hsa_circ_191016,RMVar_hsa_circ_191017 111358 RMVar_ID_111358 Human_SNP_ID_832596008 m1A Human chr19 + 39971230 39971230 39971230 TCACTATGGAGGAGATAGGCATCTTGGTGGAGAAGGCTCAGGTACAGTGGGGACTTGGGCTTTTT TCACTATGGAGGAGATAGGCATCTTGGTGGAGGAGGCTCAGGTACAGTGGGGACTTGGGCTTTTT A G PSMC4 Ensembl:ENSG00000013275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:39971176..39971296;chr19:39971176..39971364 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_1565358,Human_RBP_ID_1887735,Human_RBP_ID_4558446,Human_RBP_ID_5320372,Human_RBP_ID_6762911,Human_RBP_ID_8840038,Human_RBP_ID_22446753,Human_RBP_ID_26336291 Human_Splice_Rec_2006935,Human_Splice_Rec_2006955,Human_Splice_Rec_2006973,Human_Splice_Rec_2006993,Human_Splice_Rec_2007011 111359 RMVar_ID_111359 Human_SNP_ID_832596574 m1A Human chr19 - 5600180 5600180 5600180 GCCTGAAGACATTAAGAAGGAAGAAAAAGACCAGGATGAGCTGAAACCCGGACCTACAAATCGGT GCCTGAAGACATTAAGAAGGAAGAAAAAGACCTGGATGAGCTGAAACCCGGACCTACAAATCGGT T A SAFB2 Ensembl:ENSG00000130254 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5600076..5600206 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_53883,Human_RBP_ID_908343,Human_RBP_ID_1575206,Human_RBP_ID_1891810,Human_RBP_ID_3954248,Human_RBP_ID_6784091,Human_RBP_ID_8493905,Human_RBP_ID_9380150,Human_RBP_ID_13510179,Human_RBP_ID_18532643,Human_RBP_ID_24545394,Human_RBP_ID_26335295,Human_RBP_ID_27814949 Human_Splice_Rec_1942138,Human_Splice_Rec_1942139,Human_Splice_Rec_1942173,Human_Splice_Rec_1942188,Human_Splice_Rec_1942189,Human_Splice_Rec_1942198,Human_Splice_Rec_1942204,Human_Splice_Rec_1942212 RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_12752,RMVar_hsa_circ_265514,RMVar_hsa_circ_191705,RMVar_hsa_circ_18988,RMVar_hsa_circ_116787,RMVar_hsa_circ_339050,RMVar_hsa_circ_191704,RMVar_hsa_circ_358881,RMVar_hsa_circ_303503,RMVar_hsa_circ_266814 111360 RMVar_ID_111360 Human_SNP_ID_832598269 m1A Human chr19 + 11021801 11021801 11021801 GAACCACCACTGCAAGCTGACGCAGGTGCTCAACACGCACTATGTGGCACCCCGCCGCCTGCTGC GAACCACCACTGCAAGCTGACGCAGGTGCTCAGCACGCACTATGTGGCACCCCGCCGCCTGCTGC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11021751..11021800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 18 lung Human_RBP_ID_53723,Human_RBP_ID_9382013 Human_Splice_Rec_1956900,Human_Splice_Rec_1956968,Human_Splice_Rec_1957034,Human_Splice_Rec_1957104,Human_Splice_Rec_1957172,Human_Splice_Rec_1957238,Human_Splice_Rec_1957302,Human_Splice_Rec_1957370,Human_Splice_Rec_1957434,Human_Splice_Rec_1957502,Human_Splice_Rec_1957570,Human_Splice_Rec_1957646,Human_Splice_Rec_1957714,Human_Splice_Rec_1957780,Human_Splice_Rec_1957846,Human_Splice_Rec_1957912,Human_Splice_Rec_1957978,Human_Splice_Rec_1958040,Human_Splice_Rec_1958108,Human_Splice_Rec_1958150,Human_Splice_Rec_1958204,Human_Splice_Rec_1958258,Human_Splice_Rec_1958308,Human_Splice_Rec_1958358,Human_Splice_Rec_1958410,Human_Splice_Rec_1958460,Human_Splice_Rec_1958512,Human_Splice_Rec_1958542,Human_Splice_Rec_1958590,Human_Splice_Rec_1958630,Human_Splice_Rec_1958676,Human_Splice_Rec_1958726,Human_Splice_Rec_1958776,Human_Splice_Rec_1958816,Human_Splice_Rec_1958838,Human_Splice_Rec_1958878,Human_Splice_Rec_1958916,Human_Splice_Rec_1958950,Human_Splice_Rec_1958956,Human_Splice_Rec_1958960,Human_Splice_Rec_1958992 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_29226,RMVar_hsa_circ_50691,RMVar_hsa_circ_58707 111361 RMVar_ID_111361 Human_SNP_ID_832598593 m1A Human chr19 + 41276261 41276261 41276261 TGCATACCTGTGGTCAGGAGCCCGTGCCAGCTATGGGGTCAGAAGGGGCCGTGTATGCTTCGAGA TGCATACCTGTGGTCAGGAGCCCGTGCCAGCTGTGGGGTCAGAAGGGGCCGTGTATGCTTCGAGA A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41276211..41276344 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 10 liver Human_RBP_ID_522419,Human_RBP_ID_1016325,Human_RBP_ID_1566187,Human_RBP_ID_1888397,Human_RBP_ID_4531047,Human_RBP_ID_5371818,Human_RBP_ID_6765840,Human_RBP_ID_8488373,Human_RBP_ID_8834433,Human_RBP_ID_9294434,Human_RBP_ID_17269403,Human_RBP_ID_17695824,Human_RBP_ID_17925746,Human_RBP_ID_18441477,Human_RBP_ID_26334927 Human_Splice_Rec_2010775,Human_Splice_Rec_2010803,Human_Splice_Rec_2010829,Human_Splice_Rec_2010841,Human_Splice_Rec_2010867,Human_Splice_Rec_2010891,Human_Splice_Rec_2010919,Human_Splice_Rec_2010951,Human_Splice_Rec_2010989,Human_Splice_Rec_2011017,Human_Splice_Rec_2011029,Human_Splice_Rec_2011057,Human_Splice_Rec_2011077 RMVar_hsa_circ_194998,RMVar_hsa_circ_348795,RMVar_hsa_circ_351270,RMVar_hsa_circ_331084,RMVar_hsa_circ_276078,RMVar_hsa_circ_308631,RMVar_hsa_circ_311027,RMVar_hsa_circ_306334,RMVar_hsa_circ_195000,RMVar_hsa_circ_194999,RMVar_hsa_circ_195004,RMVar_hsa_circ_354097,RMVar_hsa_circ_375137,RMVar_hsa_circ_195002,RMVar_hsa_circ_277653,RMVar_hsa_circ_47888,RMVar_hsa_circ_274661 111362 RMVar_ID_111362 Human_SNP_ID_832598956 m1A Human chr19 + 12943810 12943810 12943810 CAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGACAAGGAGGATGATGAGGACAAAGATGAGGATG CAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGCCAAGGAGGATGATGAGGACAAAGATGAGGATG A C CALR Ensembl:ENSG00000179218 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:12943647..12943977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_513626,Human_RBP_ID_825947,Human_RBP_ID_1880274,Human_RBP_ID_2556495,Human_RBP_ID_3563361,Human_RBP_ID_4562194,Human_RBP_ID_5116727,Human_RBP_ID_5145674,Human_RBP_ID_5190510,Human_RBP_ID_5585366,Human_RBP_ID_6721337,Human_RBP_ID_8198600,Human_RBP_ID_8477509,Human_RBP_ID_9346687,Human_RBP_ID_13372468,Human_RBP_ID_17655531,Human_RBP_ID_17694632,Human_RBP_ID_17915376,Human_RBP_ID_18208591,Human_RBP_ID_18532274,Human_RBP_ID_18722846,Human_RBP_ID_22966984,Human_RBP_ID_23130708,Human_RBP_ID_23174156,Human_RBP_ID_23783076,Human_RBP_ID_24483541,Human_RBP_ID_24545443,Human_RBP_ID_24552816,Human_RBP_ID_26335809,Human_RBP_ID_26464659,Human_RBP_ID_26983149,Human_RBP_ID_27463687,Human_RBP_ID_27815188 Human_Splice_Rec_1964392,Human_Splice_Rec_1964416,Human_Splice_Rec_1964418 Human_miRNA_ID_2255656,Human_miRNA_ID_2255657,Human_miRNA_ID_2571379,Human_miRNA_ID_2571380,Human_miRNA_ID_3045115,Human_miRNA_ID_3045116 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_110485,RMVar_hsa_circ_192843,RMVar_hsa_circ_192844,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_81328,RMVar_hsa_circ_192849,RMVar_hsa_circ_192851,RMVar_hsa_circ_76392,RMVar_hsa_circ_192853,RMVar_hsa_circ_192854,RMVar_hsa_circ_110866,RMVar_hsa_circ_192855,RMVar_hsa_circ_378042 111363 RMVar_ID_111363 Human_SNP_ID_832598968 m1A Human chr19 + 12943810 12943810 12943810 CAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGACAAGGAGGATGATGAGGACAAAGATGAGGATG CAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGGCAAGGAGGATGATGAGGACAAAGATGAGGATG A G CALR Ensembl:ENSG00000179218 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:12943647..12943977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus Human_RBP_ID_513626,Human_RBP_ID_825947,Human_RBP_ID_1880274,Human_RBP_ID_2556495,Human_RBP_ID_3563361,Human_RBP_ID_4562194,Human_RBP_ID_5116727,Human_RBP_ID_5145674,Human_RBP_ID_5190510,Human_RBP_ID_5585366,Human_RBP_ID_6721337,Human_RBP_ID_8198600,Human_RBP_ID_8477509,Human_RBP_ID_9346687,Human_RBP_ID_13372468,Human_RBP_ID_17655531,Human_RBP_ID_17694632,Human_RBP_ID_17915376,Human_RBP_ID_18208591,Human_RBP_ID_18532274,Human_RBP_ID_18722846,Human_RBP_ID_22966984,Human_RBP_ID_23130708,Human_RBP_ID_23174156,Human_RBP_ID_23783076,Human_RBP_ID_24483541,Human_RBP_ID_24545443,Human_RBP_ID_24552816,Human_RBP_ID_26335809,Human_RBP_ID_26464659,Human_RBP_ID_26983149,Human_RBP_ID_27463687,Human_RBP_ID_27815188 Human_Splice_Rec_1964392,Human_Splice_Rec_1964416,Human_Splice_Rec_1964418 Human_miRNA_ID_2255656,Human_miRNA_ID_2255657,Human_miRNA_ID_2571379,Human_miRNA_ID_2571380,Human_miRNA_ID_3045115,Human_miRNA_ID_3045116 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_110485,RMVar_hsa_circ_192843,RMVar_hsa_circ_192844,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_81328,RMVar_hsa_circ_192849,RMVar_hsa_circ_192851,RMVar_hsa_circ_76392,RMVar_hsa_circ_192853,RMVar_hsa_circ_192854,RMVar_hsa_circ_110866,RMVar_hsa_circ_192855,RMVar_hsa_circ_378042 111364 RMVar_ID_111364 Human_SNP_ID_832603602 m1A Human chr19 - 55456491 55456491 55456491 GGGCCTGACCCACCGTCCCTCTGCCCACCCCCAGAAAATGGCGGCTGCCAGGCCCAGCCTGGGCC GGGCCTGACCCACCGTCCCTCTGCCCACCCCCGGAAAATGGCGGCTGCCAGGCCCAGCCTGGGCC T C ISOC2 Ensembl:ENSG00000063241 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:55456450..55456535 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_4559894,Human_RBP_ID_5116425 111365 RMVar_ID_111365 Human_SNP_ID_832605944 m1A Human chr19 - 49670261 49670261 49670261 GAACAGCTCCACCAGGCGGGCGAAAGAGTCGGAGGACAGGCGGACCAGCTTGCTGCGCAGGGCGG GAACAGCTCCACCAGGCGGGCGAAAGAGTCGGGGGACAGGCGGACCAGCTTGCTGCGCAGGGCGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49670251..49670400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 111366 RMVar_ID_111366 Human_SNP_ID_832611475 m1A Human chr19 + 48629248 48629248 48629248 CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCAGCTCTACACTCACCCGTCTCCGAAGGGGCCCC CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCCGCTCTACACTCACCCGTCTCCGAAGGGGCCCC A C SPHK2 Ensembl:ENSG00000063176 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48629199..48629349 26863196 MeRIP-seq:(Medium) rs747894513 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_27470099 111367 RMVar_ID_111367 Human_SNP_ID_832611537 m1A Human chr19 + 48629248 48629248 48629248 CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCAGCTCTACACTCACCCGTCTCCGAAGGGGCCCC CTGCTGTCTTCACCTCCTGGCTCTCCCAAGGCGGCTCTACACTCACCCGTCTCCGAAGGGGCCCC A G SPHK2 Ensembl:ENSG00000063176 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48629199..48629349 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_27470099 111368 RMVar_ID_111368 Human_SNP_ID_832615730 m1A Human chr19 - 42370883 42370883 42370883 GCTCCAGAGCTACTCCCAGTGAGAAGGGTGGGATCCCCGGCCTCCCCCCCCCCCCCCCCCCCCCC GCTCCAGAGCTACTCCCAGTGAGAAGGGTGGGGTCCCCGGCCTCCCCCCCCCCCCCCCCCCCCCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:42370747..42370900;chr19:42370826..42370900 26863196 MeRIP-seq:(Medium) rs1214416279 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 3 oesophagus 111369 RMVar_ID_111369 Human_SNP_ID_832616071 m1A Human chr19 - 49595075 49595075 49595075 CAGCGGCGGCGGCAGCGGAAGAGGAAGCCAGCAGGTTGAACTGAGTTGGGAGGTGGCGAGGAGGT CAGCGGCGGCGGCAGCGGAAGAGGAAGCCAGCGGGTTGAACTGAGTTGGGAGGTGGCGAGGAGGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49595051..49595075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 111370 RMVar_ID_111370 Human_SNP_ID_832619449 m1A Human chr19 - 14469475 14469474 14469475 GCTCAGAGAACACGTCGCTGTGGATGTGCAGCATCAGGTCCCCACCGGCCGAGTACTCCATCACG GCTCAGAGAACACGTCGCTGTGGATGTGCAGC_TCAGGTCCCCACCGGCCGAGTACTCCATCACG AT A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14469426..14469500 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 OV 1 - 111371 RMVar_ID_111371 Human_SNP_ID_832620886 m1A Human chr19 - 34400147 34400147 34400147 CCTTCCCTGCTAAGGGCTCGTGGTCCAAGCCCACAACCAGAGGGTGCTCTGGGTGGTGTCCAGGA CCTTCCCTGCTAAGGGCTCGTGGTCCAAGCCCGCAACCAGAGGGTGCTCTGGGTGGTGTCCAGGA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:34400100..34400213 26863196 MeRIP-seq:(Medium) rs980518904 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 111372 RMVar_ID_111372 Human_SNP_ID_832621809 m1A Human chr19 + 40192612 40192612 40192612 CAGGGTGCTGGCAGGTCGCCGGGTGCCACCTCACGTGCTGGTCAACTGGGCTGTGCAGGTGGCCC CAGGGTGCTGGCAGGTCGCCGGGTGCCACCTCGCGTGCTGGTCAACTGGGCTGTGCAGGTGGCCC A G MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40191941..40204624 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_82002,RMVar_hsa_circ_194828 111373 RMVar_ID_111373 Human_SNP_ID_832625304 m1A Human chr19 - 1615679 1615679 1615679 CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAACCCACCCCTCGGCACTCCCCACCCTCACCCCA CTGAAGGCCCCCCGGGCCCGGACCAGGTGCCAGCCCACCCCTCGGCACTCCCCACCCTCACCCCA T C TCF3 Ensembl:ENSG00000071564 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1615676..1615825 26863196 MeRIP-seq:(Medium) rs773006419 Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_99682,RMVar_hsa_circ_267745,RMVar_hsa_circ_34083,RMVar_hsa_circ_117817,RMVar_hsa_circ_376315,RMVar_hsa_circ_110050,RMVar_hsa_circ_191105,RMVar_hsa_circ_191107,RMVar_hsa_circ_20287,RMVar_hsa_circ_191106,RMVar_hsa_circ_191104 111374 RMVar_ID_111374 Human_SNP_ID_832627128 m1A Human chr19 - 15264648 15264648 15264648 GCCCAAGACCACCAAGCTGGGCCAGCGGCGGGAGAGCAGCCGGCCTGTGAAACCTCCAAAGAAGG GCCCAAGACCACCAAGCTGGGCCAGCGGCGGGGGAGCAGCCGGCCTGTGAAACCTCCAAAGAAGG T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:15264601..15265650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_240369,Human_RBP_ID_9293489,Human_RBP_ID_17387274,Human_RBP_ID_22230436,Human_RBP_ID_26335908,Human_RBP_ID_27816226 Human_miRNA_ID_2778433 RMVar_hsa_circ_107707,RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 111375 RMVar_ID_111375 Human_SNP_ID_832630981 m1A Human chr19 + 3530477 3530475 3530477 CGCATGGGAGAGCGCATGGATGAGCGCATGGGAGAGCGCATGGGTGAGCGGATGCAAGAGTGGAT CGCATGGGAGAGCGCATGGATGAGCGCATGG__GAGCGCATGGGTGAGCGGATGCAAGAGTGGAT GGA G FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:3529926..3530743 26863196 MeRIP-seq:(Medium) rs200953287 Functional Loss DEL ICGC 32..33 33 PBCA 1 - Human_RBP_ID_23793151 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 111376 RMVar_ID_111376 Human_SNP_ID_832631708 m1A Human chr19 - 40447971 40447971 40447971 ACGAGGGCCCTCAAGGGTCATCTCCAAACATGACCTGGGCCATTTCATGCTGCGCTGCCTCACCA ACGAGGGCCCTCAAGGGTCATCTCCAAACATGGCCTGGGCCATTTCATGCTGCGCTGCCTCACCA T C BLVRB Ensembl:ENSG00000090013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40447923..40447994 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_137324,Human_RBP_ID_4529972 Human_Splice_Rec_2008228,Human_Splice_Rec_2008234,Human_Splice_Rec_2008238,Human_Splice_Rec_2008244,Human_Splice_Rec_2008248,Human_Splice_Rec_2008254 Human_miRNA_ID_1938494,Human_miRNA_ID_1949594 RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_114022,RMVar_hsa_circ_194861 111377 RMVar_ID_111377 Human_SNP_ID_832634579 m1A Human chr19 - 49665675 49665675 49665675 TCGAGTTTGAGAGCTACCCGGAGCTCCAAGACAGGGGTGGGTTCCAGCTGCCCGCACGCCCCGAC TCGAGTTTGAGAGCTACCCGGAGCTCCAAGACGGGGGTGGGTTCCAGCTGCCCGCACGCCCCGAC T C IRF3 Ensembl:ENSG00000126456 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49665624..49665733 32194978 MeRIP-seq:(Medium) rs563734774 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1017565 Human_Splice_Rec_2031297,Human_Splice_Rec_2031331,Human_Splice_Rec_2031339,Human_Splice_Rec_2031353,Human_Splice_Rec_2031395,Human_Splice_Rec_2031407,Human_Splice_Rec_2031421,Human_Splice_Rec_2031431,Human_Splice_Rec_2031439,Human_Splice_Rec_2031449,Human_Splice_Rec_2031477,Human_Splice_Rec_2031487,Human_Splice_Rec_2031495,Human_Splice_Rec_2031505,Human_Splice_Rec_2031513,Human_Splice_Rec_2031529,Human_Splice_Rec_2031535,Human_Splice_Rec_2031559 111378 RMVar_ID_111378 Human_SNP_ID_832646027 m1A Human chr19 - 18280831 18280831 18280831 GGGGGCGCCGCGACGGTCGCCTTCGCTGCCGAACCTGTGCCCTTCCCGCCGCCGCCACCCCCAGG GGGGGCGCCGCGACGGTCGCCTTCGCTGCCGATCCTGTGCCCTTCCCGCCGCCGCCACCCCCAGG T A JUND Ensembl:ENSG00000130522 Protein coding CDS GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:18280739..18280993 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_516101,Human_RBP_ID_5421263,Human_RBP_ID_6726593,Human_RBP_ID_8830507,Human_RBP_ID_22070001,Human_RBP_ID_22533137,Human_RBP_ID_27270103,Human_RBP_ID_27465326,Human_RBP_ID_27562160 111379 RMVar_ID_111379 Human_SNP_ID_832647366 m1A Human chr19 - 14120450 14120450 14120450 GAGAACTCCATGGACTGCATCTAACTGCAGGAACCCAGAGTGTCCCAGCACGCCGGGAGGGGCAA GAGAACTCCATGGACTGCATCTAACTGCAGGAGCCCAGAGTGTCCCAGCACGCCGGGAGGGGCAA T C ASF1B Ensembl:ENSG00000105011 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:14120194..14120675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_514114,Human_RBP_ID_1555284,Human_RBP_ID_5146216,Human_RBP_ID_17266794 Human_miRNA_ID_935841,Human_miRNA_ID_955819,Human_miRNA_ID_2425600,Human_miRNA_ID_2435268,Human_miRNA_ID_2784717 RMVar_hsa_circ_92962,RMVar_hsa_circ_112658,RMVar_hsa_circ_95845,RMVar_hsa_circ_192976,RMVar_hsa_circ_192977,RMVar_hsa_circ_192975 111380 RMVar_ID_111380 Human_SNP_ID_832650612 m1A Human chr19 + 5787202 5787202 5787202 ACCTACAGGACGGTGGTGGGAGGTGGTGGGAGATGGTGGGAGGTGGTGGGAGACGGTGGGAGGTG ACCTACAGGACGGTGGTGGGAGGTGGTGGGAGGTGGTGGGAGGTGGTGGGAGACGGTGGGAGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5787173..5787257 26863196 MeRIP-seq:(Medium) rs796405103 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 111381 RMVar_ID_111381 Human_SNP_ID_832650674 m1A Human chr19 + 6591001 6591001 6591001 GCCGCACCGAGCAGCCCGAACCCTCCTCCGGCATCGCCGCGGCGATCACCTCCGCTAGCGCAGGA GCCGCACCGAGCAGCCCGAACCCTCCTCCGGCTTCGCCGCGGCGATCACCTCCGCTAGCGCAGGA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6590951..6591150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 4 haematopoietic and lymphoid tissue 111382 RMVar_ID_111382 Human_SNP_ID_832650908 m1A Human chr19 + 38723696 38723696 38723696 TCTGTGACCAGTGGGACGCCCTCGGCTCTCTGACACATAGTCGCAGGGAAGCCCTGGAGGTGAGG TCTGTGACCAGTGGGACGCCCTCGGCTCTCTGGCACATAGTCGCAGGGAAGCCCTGGAGGTGAGG A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:38723601..38723725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_1015686,Human_RBP_ID_6759830,Human_RBP_ID_8833549,Human_RBP_ID_9293651,Human_RBP_ID_22446700,Human_RBP_ID_22971831 Human_Splice_Rec_2003482,Human_Splice_Rec_2003483,Human_Splice_Rec_2003508,Human_Splice_Rec_2003509,Human_Splice_Rec_2003531 RMVar_hsa_circ_194638,RMVar_hsa_circ_77110,RMVar_hsa_circ_62920,RMVar_hsa_circ_124795,RMVar_hsa_circ_194648,RMVar_hsa_circ_117529,RMVar_hsa_circ_194651,RMVar_hsa_circ_52375,RMVar_hsa_circ_356791,RMVar_hsa_circ_124372,RMVar_hsa_circ_194657 111383 RMVar_ID_111383 Human_SNP_ID_832651431 m1A Human chr19 + 48999370 48999370 48999370 CGGAGATCCGTGATGTAACAAGGATTGAGCGAATCGGTGAGTGAGTTGGGTCAGGAATAGGACCT CGGAGATCCGTGATGTAACAAGGATTGAGCGATTCGGTGAGTGAGTTGGGTCAGGAATAGGACCT A T RUVBL2 Ensembl:ENSG00000183207 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48999301..48999435 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 4 breast Human_RBP_ID_3957299,Human_RBP_ID_4558657,Human_RBP_ID_5370583,Human_RBP_ID_19093931,Human_RBP_ID_23804096 Human_Splice_Rec_2028242,Human_Splice_Rec_2028243,Human_Splice_Rec_2028276,Human_Splice_Rec_2028277,Human_Splice_Rec_2028308,Human_Splice_Rec_2028309,Human_Splice_Rec_2028314,Human_Splice_Rec_2028315,Human_Splice_Rec_2028330,Human_Splice_Rec_2028332,Human_Splice_Rec_2028333,Human_Splice_Rec_2028360,Human_Splice_Rec_2028361,Human_Splice_Rec_2028388,Human_Splice_Rec_2028389,Human_Splice_Rec_2028401,Human_Splice_Rec_2028403,Human_Splice_Rec_2028407 RMVar_hsa_circ_97413,RMVar_hsa_circ_102952,RMVar_hsa_circ_195775,RMVar_hsa_circ_99196,RMVar_hsa_circ_195774,RMVar_hsa_circ_195776 111384 RMVar_ID_111384 Human_SNP_ID_832655787 m1A Human chr19 - 1269409 1269409 1269409 TCCTCGGAGCCGGTGCAGCCAGGGCCCTCACCACTGAGTCGGGCAGGTCCCTGACGCAAGCGGGA TCCTCGGAGCCGGTGCAGCCAGGGCCCTCACCGCTGAGTCGGGCAGGTCCCTGACGCAAGCGGGA T C CIRBP-AS1 Ensembl:ENSG00000267493 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:1269398..1270950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 28 large intestine Human_RBP_ID_5587813 111385 RMVar_ID_111385 Human_SNP_ID_832656272 m1A Human chr19 + 46757057 46757055 46757058 GCGGAGAGGGGAAGGGGGAAACTGACCAAGAAAGAAATTCTAAGGAGAGCATGAGAGAAGGCTGG GCGGAGAGGGGAAGGGGGAAACTGACCAAGA___AAATTCTAAGGAGAGCATGAGAGAAGGCTGG AAAG A FKRP Ensembl:ENSG00000181027 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:46757007..46757141 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 ACC 1 - Human_RBP_ID_5527063,Human_RBP_ID_22072038 111386 RMVar_ID_111386 Human_SNP_ID_832656358 m1A Human chr19 + 49107878 49107878 49107878 GGAGCGCAGAGAGCGGAGCCGGGAGCGAGACAAGGAGCGAGAACGGCGACGCTCCCGCTCCCGGG GGAGCGCAGAGAGCGGAGCCGGGAGCGAGACACGGAGCGAGAACGGCGACGCTCCCGCTCCCGGG A C SNRNP70 Ensembl:ENSG00000104852 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49104548..49108400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 READ 1 - Human_RBP_ID_22446939,Human_RBP_ID_22977502 Human_Splice_Rec_2028580,Human_Splice_Rec_2028616,Human_Splice_Rec_2028636,Human_Splice_Rec_2028654,Human_Splice_Rec_2028674,Human_Splice_Rec_2028696 111387 RMVar_ID_111387 Human_SNP_ID_832656871 m1A Human chr19 - 14496076 14496076 14496076 GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC GCCGAGCCGGGTGCGCACGGGGAGGCGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C GIPC1 Ensembl:ENSG00000123159 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr19:14491651..14496149;chr19:14491613..14496125;chr19:14491578..14496150 26863410,26863196 MeRIP-seq:(Medium) rs540479273 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_239973,Human_RBP_ID_771112,Human_RBP_ID_4557281 Human_Splice_Rec_1968831,Human_Splice_Rec_1968841,Human_Splice_Rec_1968857,Human_Splice_Rec_1968879,Human_Splice_Rec_1968893,Human_Splice_Rec_1968905,Human_Splice_Rec_1968917 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026 111388 RMVar_ID_111388 Human_SNP_ID_832667450 m1A Human chr19 + 50398961 50398961 50398961 TGATGCACCTCGGCCATCCCAATTCGAGGAGGACCTGGCACTGATGGAGGAGATGGAGGCAGAAC TGATGCACCTCGGCCATCCCAATTCGAGGAGGGCCTGGCACTGATGGAGGAGATGGAGGCAGAAC A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:50398851..50398991 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas insulinoma 4 pancreas Human_RBP_ID_1570071,Human_RBP_ID_1891155,Human_RBP_ID_5585865,Human_RBP_ID_6779819,Human_RBP_ID_8492564,Human_RBP_ID_8840186,Human_RBP_ID_9294536,Human_RBP_ID_17935080,Human_RBP_ID_18998621,Human_RBP_ID_22975541,Human_RBP_ID_23805224 Human_Splice_Rec_2035449,Human_Splice_Rec_2035499,Human_Splice_Rec_2035551,Human_Splice_Rec_2035605,Human_Splice_Rec_2035659,Human_Splice_Rec_2035705,Human_Splice_Rec_2035757,Human_Splice_Rec_2035809,Human_Splice_Rec_2035825 Human_miRNA_ID_2769381 RMVar_hsa_circ_76877,RMVar_hsa_circ_195993,RMVar_hsa_circ_195992,RMVar_hsa_circ_287397,RMVar_hsa_circ_195994,RMVar_hsa_circ_280249 111389 RMVar_ID_111389 Human_SNP_ID_832668428 m1A Human chr19 + 12948333 12948333 12948333 AGGACAAGAGCCCATCAGAGGAATCCGCCCCCACGACGTCCCCAGAGTCTGTGTCAGGGTAAGGC AGGACAAGAGCCCATCAGAGGAATCCGCCCCCGCGACGTCCCCAGAGTCTGTGTCAGGGTAAGGC A G RAD23A Ensembl:ENSG00000179262 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12948282..12948444 26863196 MeRIP-seq:(Medium) rs11558955 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_513663,Human_RBP_ID_772193,Human_RBP_ID_826039,Human_RBP_ID_3954555,Human_RBP_ID_17915393 Human_Splice_Rec_1964427,Human_Splice_Rec_1964441,Human_Splice_Rec_1964457,Human_Splice_Rec_1964473,Human_Splice_Rec_1964483,Human_Splice_Rec_1964499,Human_Splice_Rec_1964513,Human_Splice_Rec_1964529 Human_miRNA_ID_2425597,Human_miRNA_ID_2435265,Human_miRNA_ID_2784715 GWAS_ID_9621,GWAS_ID_9622,GWAS_ID_9623,GWAS_ID_9624 RMVar_hsa_circ_425,RMVar_hsa_circ_192856,RMVar_hsa_circ_315860 111390 RMVar_ID_111390 Human_SNP_ID_832670298 m1A Human chr19 - 13961107 13961106 13961108 CCCTGCCCAGCCCCGTTCCGCAGGCTAACACTAGTGCCGGTCATCAGTCGGTGGGCCAGCCGGCC CCCTGCCCAGCCCCGTTCCGCAGGCTAACAC__GTGCCGGTCATCAGTCGGTGGGCCAGCCGGCC CTA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13961057..13961132 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 HNSC 1 - 111391 RMVar_ID_111391 Human_SNP_ID_832673199 m1A Human chr19 + 6750552 6750552 6750552 AGCCTCCCTCAGAAGAGAGCCAGGACACCCCCATTTACACGGAGTTTGATGAGGATTTCGAGGAG AGCCTCCCTCAGAAGAGAGCCAGGACACCCCCGTTTACACGGAGTTTGATGAGGATTTCGAGGAG A G TRIP10 Ensembl:ENSG00000125733 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:6750276..6750608 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_23211155,Human_RBP_ID_27562928 Human_Splice_Rec_1945724,Human_Splice_Rec_1945725,Human_Splice_Rec_1945756,Human_Splice_Rec_1945757,Human_Splice_Rec_1945784,Human_Splice_Rec_1945785,Human_Splice_Rec_1945812,Human_Splice_Rec_1945813,Human_Splice_Rec_1945837,Human_Splice_Rec_1945862,Human_Splice_Rec_1945863 Human_miRNA_ID_2465222 RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_191915,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_77437,RMVar_hsa_circ_191913,RMVar_hsa_circ_293256,RMVar_hsa_circ_317844,RMVar_hsa_circ_191914,RMVar_hsa_circ_337150 111392 RMVar_ID_111392 Human_SNP_ID_832674598 m1A Human chr19 - 3977503 3977503 3977503 CACCGCGGAGGGGGCCAGATCATCCCCACAGCACGGCGCTGCCTCTATGCCAGTGTGCTGACCGC CACCGCGGAGGGGGCCAGATCATCCCCACAGCTCGGCGCTGCCTCTATGCCAGTGTGCTGACCGC T A EEF2 Ensembl:ENSG00000167658 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3977197..3977630 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_521437,Human_RBP_ID_771946,Human_RBP_ID_1015832,Human_RBP_ID_1564594,Human_RBP_ID_3571501,Human_RBP_ID_4527006,Human_RBP_ID_6760958,Human_RBP_ID_8486979,Human_RBP_ID_8833715,Human_RBP_ID_13452329,Human_RBP_ID_17695621,Human_RBP_ID_18191780,Human_RBP_ID_18732111,Human_RBP_ID_22810715,Human_RBP_ID_26989637,Human_RBP_ID_27273964,Human_RBP_ID_27467877 Human_Splice_Rec_1938843 RMVar_hsa_circ_76099,RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_79883,RMVar_hsa_circ_88674,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191439,RMVar_hsa_circ_191440,RMVar_hsa_circ_191438,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_370612,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_191449,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_281483,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452 111393 RMVar_ID_111393 Human_SNP_ID_832674833 m1A Human chr19 + 55347034 55347034 55347034 CACCTCACCCCTCTGGCTCCAGTGGCTGCCTCAGCCCCAGCCCCGAGTGCGGCCCCGGAAGCGCC CACCTCACCCCTCTGGCTCCAGTGGCTGCCTCGGCCCCAGCCCCGAGTGCGGCCCCGGAAGCGCC A G KMT5C Ensembl:ENSG00000133247 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55346562..55347482 26863196 MeRIP-seq:(Medium) rs1324240717 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_2047350,Human_Splice_Rec_2047368,Human_Splice_Rec_2047384,Human_Splice_Rec_2047420 Human_miRNA_ID_1358605 RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_93230,RMVar_hsa_circ_196324 111394 RMVar_ID_111394 Human_SNP_ID_832677748 m1A Human chr19 + 47701788 47701788 47701788 GTGGCCGAGCCCCCGCCACGGCCGCCACCACCACCGCCGCCCACGGGCCAGATGAACGGCACGGT GTGGCCGAGCCCCCGCCACGGCCGCCACCACCGCCGCCGCCCACGGGCCAGATGAACGGCACGGT A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:47701745..47701993 26863196 MeRIP-seq:(Medium) rs1568581830 Functional Loss SNV ICGC 33..33 33 STAD 1 - 111395 RMVar_ID_111395 Human_SNP_ID_832678949 m1A Human chr19 - 4653363 4653363 4653363 AATCTTCCTGCCTCGGCCTCCCAAAGTGCTGGAATTAGAGTAGTGAGCCACTGCACGTGGCCTCA AATCTTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTAGAGTAGTGAGCCACTGCACGTGGCCTCA T C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4653313..4653382 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_13477935 111396 RMVar_ID_111396 Human_SNP_ID_832681556 m1A Human chr19 - 36114390 36114390 36114390 CCTCTCGTAGTGCCGGAACTGTGATTACCAGCAGGAGGCCGACAACAGCTGCATCTATGTCAACA CCTCTCGTAGTGCCGGAACTGTGATTACCAGCCGGAGGCCGACAACAGCTGCATCTATGTCAACA T G POLR2I Ensembl:ENSG00000105258 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr19:36114176..36114468;chr19:36114326..36114442;chr19:36114326..36114425 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_520379,Human_RBP_ID_1561614,Human_RBP_ID_1884895,Human_RBP_ID_9380945,Human_RBP_ID_18946784,Human_RBP_ID_19090010,Human_RBP_ID_23793811,Human_RBP_ID_26815728 Human_Splice_Rec_1997760,Human_Splice_Rec_1997761,Human_Splice_Rec_1997768,Human_Splice_Rec_1997769,Human_Splice_Rec_1997776,Human_Splice_Rec_1997777,Human_Splice_Rec_1997786,Human_Splice_Rec_1997787,Human_Splice_Rec_1997795,Human_Splice_Rec_1997804,Human_Splice_Rec_1997805,Human_Splice_Rec_1997811 Human_miRNA_ID_2013998,Human_miRNA_ID_2513241,Human_miRNA_ID_3056059 RMVar_hsa_circ_101538,RMVar_hsa_circ_123799,RMVar_hsa_circ_194362,RMVar_hsa_circ_194363,RMVar_hsa_circ_297221 111397 RMVar_ID_111397 Human_SNP_ID_832682378 m1A Human chr19 - 4502118 4502118 4502118 TAGGCAGGAAAAAAAAACCCAAGGGAACAAATACAAACAGCACAGCGTTCCCCACAGTTCTCTGC TAGGCAGGAAAAAAAAACCCAAGGGAACAAATGCAAACAGCACAGCGTTCCCCACAGTTCTCTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4501560..4502175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111398 RMVar_ID_111398 Human_SNP_ID_832686376 m1A Human chr19 + 42419520 42419520 42419520 GAATCCCTGGCAGAGGGCACTGGGGCAGGGGTAGGCCCACTGGGGCCGTGGGTAAGGACTAGGGG GAATCCCTGGCAGAGGGCACTGGGGCAGGGGTGGGCCCACTGGGGCCGTGGGTAAGGACTAGGGG A G LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:42419506..42419582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_5248998 111399 RMVar_ID_111399 Human_SNP_ID_832695348 m1A Human chr19 + 48473377 48473377 48473377 AGTTCACCGACCTCAATCTGGTGCAGGCCCTCAGGTGAGTGAGGGGGAGGGGTTTGGAACGCCAG AGTTCACCGACCTCAATCTGGTGCAGGCCCTCGGGTGAGTGAGGGGGAGGGGTTTGGAACGCCAG A G CYTH2 Ensembl:ENSG00000105443 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48473226..48473426 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_3955331,Human_RBP_ID_18995241,Human_RBP_ID_19090586,Human_RBP_ID_27816591 Human_Splice_Rec_2026592,Human_Splice_Rec_2026593,Human_Splice_Rec_2026612,Human_Splice_Rec_2026613,Human_Splice_Rec_2026624,Human_Splice_Rec_2026625,Human_Splice_Rec_2026646,Human_Splice_Rec_2026647,Human_Splice_Rec_2026676,Human_Splice_Rec_2026677,Human_Splice_Rec_2026698,Human_Splice_Rec_2026699,Human_Splice_Rec_2026722,Human_Splice_Rec_2026723,Human_Splice_Rec_2026728,Human_Splice_Rec_2026729,Human_Splice_Rec_2026735 RMVar_hsa_circ_195693,RMVar_hsa_circ_301198 111400 RMVar_ID_111400 Human_SNP_ID_832698218 m1A Human chr19 + 17517778 17517778 17517778 CCGAAGCCACCGCCACAGCGTGTGACCCTCACACTACCTGTCCTGAATGCAGCACGAACTGTCAT CCGAAGCCACCGCCACAGCGTGTGACCCTCACGCTACCTGTCCTGAATGCAGCACGAACTGTCAT A G PGLS Ensembl:ENSG00000130313 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6743 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 4 head and neck Human_RBP_ID_18192086,Human_RBP_ID_26817200 Human_Splice_Rec_1977152,Human_Splice_Rec_1977153,Human_Splice_Rec_1977160,Human_Splice_Rec_1977161,Human_Splice_Rec_1977170,Human_Splice_Rec_1977180,Human_Splice_Rec_1977181 Human_miRNA_ID_2061770,Human_miRNA_ID_2168887,Human_miRNA_ID_2170410,Human_miRNA_ID_2627676,Human_miRNA_ID_2748512,Human_miRNA_ID_2766094 RMVar_hsa_circ_193325,RMVar_hsa_circ_80786,RMVar_hsa_circ_295626,RMVar_hsa_circ_193329,RMVar_hsa_circ_92242,RMVar_hsa_circ_193328,RMVar_hsa_circ_321938,RMVar_hsa_circ_193330,RMVar_hsa_circ_78216 111401 RMVar_ID_111401 Human_SNP_ID_832700044 m1A Human chr19 - 43772071 43772071 43772071 ACACACTTTGGCTGATCCCCATCACATTCCTGACCATCGGCTATGGTGACGTGGTGCCGGGCACC ACACACTTTGGCTGATCCCCATCACATTCCTGGCCATCGGCTATGGTGACGTGGTGCCGGGCACC T C KCNN4 Ensembl:ENSG00000104783 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43772008..43774215 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_22763003 Human_Splice_Rec_2016024,Human_Splice_Rec_2016025,Human_Splice_Rec_2016040,Human_Splice_Rec_2016041,Human_Splice_Rec_2016052,Human_Splice_Rec_2016053,Human_Splice_Rec_2016076,Human_Splice_Rec_2016077,Human_Splice_Rec_2016088,Human_Splice_Rec_2016089,Human_Splice_Rec_2016095 RMVar_hsa_circ_34007,RMVar_hsa_circ_325025 111402 RMVar_ID_111402 Human_SNP_ID_832705595 m1A Human chr19 - 798449 798449 798449 ACTGCACGGACCACGTTTAACAGACTTTTAAAAGTGACTGAACCCAAGAAAAACTTCTCAGGAAA ACTGCACGGACCACGTTTAACAGACTTTTAAAGGTGACTGAACCCAAGAAAAACTTCTCAGGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:798445..803572 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine 111403 RMVar_ID_111403 Human_SNP_ID_832708739 m1A Human chr19 - 48327569 48327569 48327569 GGCCCATGTTTTGGTGTCGTTGTTCCACGTGCAGTCGTACCAGAGATTCAGGGACTCTTTCCCAG GGCCCATGTTTTGGTGTCGTTGTTCCACGTGCGGTCGTACCAGAGATTCAGGGACTCTTTCCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:48327501..48327600;chr19:48327501..48327575 26863196 MeRIP-seq:(Medium) rs1476209533 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 111404 RMVar_ID_111404 Human_SNP_ID_832715910 m1A Human chr19 - 48617814 48617814 48617814 AGGTTCGGCGCAAGGAGCCCAAGAGCCAGGATATCTACCTGAGGCTGTTGGTCAAGGTGAGGCTG AGGTTCGGCGCAAGGAGCCCAAGAGCCAGGATGTCTACCTGAGGCTGTTGGTCAAGGTGAGGCTG T C RPL18 Ensembl:ENSG00000063177 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:48617801..48617900 26863410 MeRIP-seq:(Medium) rs561664573 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 4 lung Human_RBP_ID_3955344,Human_RBP_ID_4558635,Human_RBP_ID_17386960,Human_RBP_ID_17656290,Human_RBP_ID_19090600,Human_RBP_ID_26816114 Human_Splice_Rec_2026958,Human_Splice_Rec_2026959,Human_Splice_Rec_2026966,Human_Splice_Rec_2026967,Human_Splice_Rec_2026975,Human_Splice_Rec_2026986,Human_Splice_Rec_2026987,Human_Splice_Rec_2026996,Human_Splice_Rec_2026997,Human_Splice_Rec_2027018,Human_Splice_Rec_2027019,Human_Splice_Rec_2027023,Human_Splice_Rec_2027034,Human_Splice_Rec_2027035,Human_Splice_Rec_2027046,Human_Splice_Rec_2027047,Human_Splice_Rec_2027056,Human_Splice_Rec_2027057,Human_Splice_Rec_2027068,Human_Splice_Rec_2027069,Human_Splice_Rec_2027078 RMVar_hsa_circ_195699,RMVar_hsa_circ_79282,RMVar_hsa_circ_89776,RMVar_hsa_circ_39397,RMVar_hsa_circ_54771,RMVar_hsa_circ_195698,RMVar_hsa_circ_128150,RMVar_hsa_circ_344171,RMVar_hsa_circ_195705 111405 RMVar_ID_111405 Human_SNP_ID_832716186 m1A Human chr19 + 20125363 20125363 20125363 CCAGAAATATGTGGATGAGGCTTCCAAGAAGGAGATCAAAGACATCCTCATCCAGTATGACCGGA CCAGAAATATGTGGATGAGGCTTCCAAGAAGGGGATCAAAGACATCCTCATCCAGTATGACCGGA A G AC011447.1,ZNF90 Ensembl:ENSG00000224864,Ensembl:ENSG00000213988 Pseudogene,Protein coding exon,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:20125325..20125420 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 KIRP 2 - Human_RBP_ID_1556959,Human_RBP_ID_9085228,Human_RBP_ID_17387663,Human_RBP_ID_17696762,Human_RBP_ID_17935985,Human_RBP_ID_26815613 Human_miRNA_ID_1024613,Human_miRNA_ID_1861491 RMVar_hsa_circ_58316 111406 RMVar_ID_111406 Human_SNP_ID_832716885 m1A Human chr19 + 48961626 48961626 48961626 AGTGCTCACCGCCTCACTCACCATCTGGAAGAAGATGGGCTGAGGCCCCCAGCTGCCTTGGACTG AGTGCTCACCGCCTCACTCACCATCTGGAAGAGGATGGGCTGAGGCCCCCAGCTGCCTTGGACTG A G BAX Ensembl:ENSG00000087088 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48961601..48961625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas Human_RBP_ID_525110,Human_RBP_ID_1890815,Human_RBP_ID_6778340,Human_RBP_ID_13493392,Human_RBP_ID_17387468,Human_RBP_ID_17656303,Human_RBP_ID_22978142,Human_RBP_ID_23804054,Human_RBP_ID_27470189 Human_Splice_Rec_2028066,Human_Splice_Rec_2028076,Human_Splice_Rec_2028084,Human_Splice_Rec_2028104,Human_Splice_Rec_2028114,Human_Splice_Rec_2028122,Human_Splice_Rec_2028128,Human_Splice_Rec_2028134 111407 RMVar_ID_111407 Human_SNP_ID_832722054 m1A Human chr19 - 49908550 49908550 49908550 CACTGGAGGAGTTGGTCAAGGAGCAGAGCGGGACCATCTACCTGCAGCACGCGGATGAGGAGCGT CACTGGAGGAGTTGGTCAAGGAGCAGAGCGGGTCCATCTACCTGCAGCACGCGGATGAGGAGCGT T A IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49908501..49908575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_1017645,Human_RBP_ID_3955473,Human_RBP_ID_5527112,Human_RBP_ID_6779455,Human_RBP_ID_22070465,Human_RBP_ID_22449614,Human_RBP_ID_26338169,Human_RBP_ID_27277373 111408 RMVar_ID_111408 Human_SNP_ID_832722503 m1A Human chr19 + 13918790 13918790 13918790 CAGACCCACCGTCACCACCGTCGCAGCCTCCGACCCCCGCTACGGCGCCCTCCACAACAGGTAGG CAGACCCACCGTCACCACCGTCGCAGCCTCCGCCCCCCGCTACGGCGCCCTCCACAACAGGTAGG A C CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:13918501..13919001;chr19:13918726..13918921 26863196 MeRIP-seq:(Medium) rs547816872 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_240337 Human_Splice_Rec_1967364,Human_Splice_Rec_1967365,Human_Splice_Rec_1967416,Human_Splice_Rec_1967417,Human_Splice_Rec_1967438,Human_Splice_Rec_1967439,Human_Splice_Rec_1967486,Human_Splice_Rec_1967487,Human_Splice_Rec_1967526,Human_Splice_Rec_1967527 RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 111409 RMVar_ID_111409 Human_SNP_ID_832722510 m1A Human chr19 + 13918790 13918790 13918790 CAGACCCACCGTCACCACCGTCGCAGCCTCCGACCCCCGCTACGGCGCCCTCCACAACAGGTAGG CAGACCCACCGTCACCACCGTCGCAGCCTCCGTCCCCCGCTACGGCGCCCTCCACAACAGGTAGG A T CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr19:13918501..13919001;chr19:13918726..13918921 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_240337 Human_Splice_Rec_1967364,Human_Splice_Rec_1967365,Human_Splice_Rec_1967416,Human_Splice_Rec_1967417,Human_Splice_Rec_1967438,Human_Splice_Rec_1967439,Human_Splice_Rec_1967486,Human_Splice_Rec_1967487,Human_Splice_Rec_1967526,Human_Splice_Rec_1967527 RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 111410 RMVar_ID_111410 Human_SNP_ID_832727750 m1A Human chr19 + 38836776 38836776 38836776 GAGAAACACAACTTCAGAGTGTAAGGGTATGGACCATCTGCAAAGGAGAGACAAGTTTGGTTGGT GAGAAACACAACTTCAGAGTGTAAGGGTATGGGCCATCTGCAAAGGAGAGACAAGTTTGGTTGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38836727..38836815 26863196 MeRIP-seq:(Medium) rs1461394671 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 111411 RMVar_ID_111411 Human_SNP_ID_832729749 m1A Human chr19 + 53873551 53873551 53873551 TTTTTGCAGCCATGCCAGTGACGGTAACCCGCACCACCATCACAACCACCACGACGTCATCTTCG TTTTTGCAGCCATGCCAGTGACGGTAACCCGCGCCACCATCACAACCACCACGACGTCATCTTCG A G MYADM Ensembl:ENSG00000179820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:53873526..53873597 26863196 MeRIP-seq:(Medium) rs781704036 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_912741,Human_RBP_ID_4558726,Human_RBP_ID_17387043,Human_RBP_ID_20417304,Human_RBP_ID_26816295 Human_Splice_Rec_2041532,Human_Splice_Rec_2041536,Human_Splice_Rec_2041540,Human_Splice_Rec_2041544,Human_Splice_Rec_2041546,Human_Splice_Rec_2041550,Human_Splice_Rec_2041554,Human_Splice_Rec_2041558,Human_Splice_Rec_2041560 RMVar_hsa_circ_104567,RMVar_hsa_circ_196212 111412 RMVar_ID_111412 Human_SNP_ID_832736998 m1A Human chr19 + 15113806 15113801 15113807 AGACTACGACCACGTGACGGGCAGTGACAGCGAGGACGAGGACGAGGAGGTCGGCGAGCCGAGGG AGACTACGACCACGTGACGGGCAGTGAC______GACGAGGACGAGGAGGTCGGCGAGCCGAGGG CAGCGAG C SYDE1 Ensembl:ENSG00000105137 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15113563..15114002 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 29..34 33 SARC 1 - Human_RBP_ID_27464305 RMVar_hsa_circ_76187,RMVar_hsa_circ_193081,RMVar_hsa_circ_193084,RMVar_hsa_circ_122544 111413 RMVar_ID_111413 Human_SNP_ID_832738011 m1A Human chr19 - 58550597 58550597 58550597 GGCCACCAGGGGAGTGGGGATGGGGTGACAGGACAGAGAACAGAGCCAGGCTGGGCTGGCCATGG GGCCACCAGGGGAGTGGGGATGGGGTGACAGGGCAGAGAACAGAGCCAGGCTGGGCTGGCCATGG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:58550401..58550675 26863196 MeRIP-seq:(Medium) rs1202777563 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 111414 RMVar_ID_111414 Human_SNP_ID_832738340 m1A Human chr19 - 43546543 43546543 43546543 GGGGCTGGGGCCTGGGCTCCTGAGTCTGAGGGAGGAGGGCCTGCGGCCTGGGCTCCTGAGTCTGA GGGGCTGGGGCCTGGGCTCCTGAGTCTGAGGGTGGAGGGCCTGCGGCCTGGGCTCCTGAGTCTGA T A XRCC1 Ensembl:ENSG00000073050 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:43546542..43546780 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_5376826 RMVar_hsa_circ_108246,RMVar_hsa_circ_103850,RMVar_hsa_circ_195156,RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195155,RMVar_hsa_circ_195159,RMVar_hsa_circ_195158,RMVar_hsa_circ_326144 111415 RMVar_ID_111415 Human_SNP_ID_832741505 m1A Human chr19 - 616828 616828 616828 AAAACGATCCTCCTCGGACGGGGGCCACCTAGAGGGTGGGGGGCGGGCGGGGCTCCACAGCCGGC AAAACGATCCTCCTCGGACGGGGGCCACCTAGGGGGTGGGGGGCGGGCGGGGCTCCACAGCCGGC T C lnc-POLRMT-2 RNACentral:URS00001BBA2A lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:616822..617150 26863196 MeRIP-seq:(Medium) rs1480419782 Functional Loss SNV ICGC 33..33 33 LAML 1 - 111416 RMVar_ID_111416 Human_SNP_ID_832742276 m1A Human chr19 - 12771220 12771220 12771220 GCCGGCCTGAAGGCGAGGGTACCCCAGGTCTCACTGCCAAGAAGCTGCTGCTGCTGCAATCCCAG GCCGGCCTGAAGGCGAGGGTACCCCAGGTCTCGCTGCCAAGAAGCTGCTGCTGCTGCAATCCCAG T C HOOK2 Ensembl:ENSG00000095066 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12771172..12771317 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_Splice_Rec_1963348,Human_Splice_Rec_1963349,Human_Splice_Rec_1963392,Human_Splice_Rec_1963393,Human_Splice_Rec_1963470,Human_Splice_Rec_1963471,Human_Splice_Rec_1963490,Human_Splice_Rec_1963491,Human_Splice_Rec_1963506,Human_Splice_Rec_1963522,Human_Splice_Rec_1963538 RMVar_hsa_circ_75656,RMVar_hsa_circ_192784,RMVar_hsa_circ_326967 111417 RMVar_ID_111417 Human_SNP_ID_832744880 m1A Human chr19 - 40242574 40242574 40242574 GTGTGGCTCCCCCAGTGACTCCTCCACGACTGAGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG GTGTGGCTCCCCCAGTGACTCCTCCACGACTGGGGAGATGGAAGTGGCGGTCAGCAAGGCACGGG T C AKT2 Ensembl:ENSG00000105221 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:40242473..40242574 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_239645,Human_RBP_ID_3955044,Human_RBP_ID_9346745,Human_RBP_ID_18733132,Human_RBP_ID_18994984,Human_RBP_ID_22977760,Human_RBP_ID_26336304,Human_RBP_ID_26770045,Human_RBP_ID_27815446 Human_Splice_Rec_2007401,Human_Splice_Rec_2007427,Human_Splice_Rec_2007453,Human_Splice_Rec_2007483,Human_Splice_Rec_2007523,Human_Splice_Rec_2007547,Human_Splice_Rec_2007577,Human_Splice_Rec_2007597,Human_Splice_Rec_2007653,Human_Splice_Rec_2007667,Human_Splice_Rec_2007681,Human_Splice_Rec_2007689,Human_Splice_Rec_2007699,Human_Splice_Rec_2007709,Human_Splice_Rec_2007717,Human_Splice_Rec_2007727,Human_Splice_Rec_2007735 RMVar_hsa_circ_2264,RMVar_hsa_circ_112632,RMVar_hsa_circ_369843,RMVar_hsa_circ_194834,RMVar_hsa_circ_194835,RMVar_hsa_circ_324315,RMVar_hsa_circ_372277,RMVar_hsa_circ_194838,RMVar_hsa_circ_194839,RMVar_hsa_circ_100928,RMVar_hsa_circ_77340,RMVar_hsa_circ_194840,RMVar_hsa_circ_194841,RMVar_hsa_circ_194843,RMVar_hsa_circ_291433,RMVar_hsa_circ_291922,RMVar_hsa_circ_126465,RMVar_hsa_circ_194844,RMVar_hsa_circ_194845 111418 RMVar_ID_111418 Human_SNP_ID_832744915 m1A Human chr19 - 58514259 58514259 58514259 CGCCGTGTGCTGGCGATCCTTCTCTCTACGCGACTACCTGCTCAAACACATGGTCACGCACACCG CGCCGTGTGCTGGCGATCCTTCTCTCTACGCGGCTACCTGCTCAAACACATGGTCACGCACACCG T C ZBTB45 Ensembl:ENSG00000119574 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:58514211..58516812 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_18741459 Human_Splice_Rec_2052138,Human_Splice_Rec_2052142,Human_Splice_Rec_2052146 111419 RMVar_ID_111419 Human_SNP_ID_832745586 m1A Human chr19 + 12807206 12807206 12807206 CTGTTCCCCTTCTCTTCCAAACCTCCTCCCAGACTCAAAGACCCTATTGGAGAGCGAGCGGGAAA CTGTTCCCCTTCTCTTCCAAACCTCCTCCCAGGCTCAAAGACCCTATTGGAGAGCGAGCGGGAAA A G THSD8,RNASEH2A Ensembl:ENSG00000284491,Ensembl:ENSG00000104889 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12807201..12807350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_910739,Human_RBP_ID_4562071,Human_RBP_ID_18996786 Human_Splice_Rec_1963638,Human_Splice_Rec_1963652,Human_Splice_Rec_1963680,Human_Splice_Rec_1963684,Human_Splice_Rec_1963694 Human_miRNA_ID_2819938 RMVar_hsa_circ_108452,RMVar_hsa_circ_358412,RMVar_hsa_circ_192795 111420 RMVar_ID_111420 Human_SNP_ID_832746559 m1A Human chr19 + 11361485 11361485 11361485 GCGGCCCTCTGCGCCTACGCGGTCACCTACACAGCGGTGAGCTTCGGGAGCTTCGGGGTCGGAAA GCGGCCCTCTGCGCCTACGCGGTCACCTACACGGCGGTGAGCTTCGGGAGCTTCGGGGTCGGAAA A G PLPPR2 Ensembl:ENSG00000105520 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11361437..11362561 32194978 MeRIP-seq:(Medium) rs764064012 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_512822,Human_RBP_ID_27463177 Human_Splice_Rec_1960145,Human_Splice_Rec_1960183,Human_Splice_Rec_1960195,Human_Splice_Rec_1960199 RMVar_hsa_circ_116024,RMVar_hsa_circ_114982,RMVar_hsa_circ_192588,RMVar_hsa_circ_9843,RMVar_hsa_circ_192590 111421 RMVar_ID_111421 Human_SNP_ID_832747950 m1A Human chr19 - 55303748 55303748 55303748 GGGAGCCACCACCCCCGGCATCGGTGATGCTCAGGACTTCCATGGACTTCCGCTCTGGTCGCCGC GGGAGCCACCACCCCCGGCATCGGTGATGCTCGGGACTTCCATGGACTTCCGCTCTGGTCGCCGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55303697..55305501 32194978 MeRIP-seq:(Medium) rs1164458618 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 5 lung 111422 RMVar_ID_111422 Human_SNP_ID_832761964 m1A Human chr19 - 16535507 16535507 16535507 CCAGGGCGCGCCATCCATGGACGAGCTCATCCAGCAGAGCCAGTGGAACCTCCAGCAGCAGGAGC CCAGGGCGCGCCATCCATGGACGAGCTCATCCGGCAGAGCCAGTGGAACCTCCAGCAGCAGGAGC T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:16535410..16535647 26863196 MeRIP-seq:(Medium) rs942072981 Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 2 stomach Human_RBP_ID_54946,Human_RBP_ID_1880954,Human_RBP_ID_3564195,Human_RBP_ID_8479107,Human_RBP_ID_18440707 Human_Splice_Rec_1973957,Human_Splice_Rec_1973989,Human_Splice_Rec_1974041 RMVar_hsa_circ_267066,RMVar_hsa_circ_378968 111423 RMVar_ID_111423 Human_SNP_ID_832763974 m1A Human chr19 + 50403551 50403551 50403551 GGACCCCGACGTGATCACCGGTTACAACATCCAGAACTTCGACCTTCCGTACCTCATCTCTCGGG GGACCCCGACGTGATCACCGGTTACAACATCCGGAACTTCGACCTTCCGTACCTCATCTCTCGGG A G POLD1 Ensembl:ENSG00000062822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50403464..50403593 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_3575401,Human_RBP_ID_8836566,Human_RBP_ID_13499792,Human_RBP_ID_17270344,Human_RBP_ID_17501239 Human_Splice_Rec_2035464,Human_Splice_Rec_2035465,Human_Splice_Rec_2035514,Human_Splice_Rec_2035515,Human_Splice_Rec_2035566,Human_Splice_Rec_2035567,Human_Splice_Rec_2035620,Human_Splice_Rec_2035621,Human_Splice_Rec_2035674,Human_Splice_Rec_2035675,Human_Splice_Rec_2035720,Human_Splice_Rec_2035721,Human_Splice_Rec_2035772,Human_Splice_Rec_2035773,Human_Splice_Rec_2035828,Human_Splice_Rec_2035829 Human_miRNA_ID_2728390 RMVar_hsa_circ_29385,RMVar_hsa_circ_76877,RMVar_hsa_circ_195992,RMVar_hsa_circ_103948,RMVar_hsa_circ_83318,RMVar_hsa_circ_195996,RMVar_hsa_circ_100166,RMVar_hsa_circ_195998,RMVar_hsa_circ_42164,RMVar_hsa_circ_195997,RMVar_hsa_circ_264883 111424 RMVar_ID_111424 Human_SNP_ID_832765173 m1A Human chr19 + 994324 994324 994324 ATCGGGACCTGTTCGACTTCTCCACGCGCTTCATCACGCGGCCGGCCAAGTGAGGCCCGGAGACC ATCGGGACCTGTTCGACTTCTCCACGCGCTTCGTCACGCGGCCGGCCAAGTGAGGCCCGGAGACC A G WDR18 Ensembl:ENSG00000065268 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:994274..994357 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_3579594,Human_RBP_ID_4556850,Human_RBP_ID_17934702 111425 RMVar_ID_111425 Human_SNP_ID_832765645 m1A Human chr19 + 38383338 38383338 38383338 GAAGCCGGAAGACACCACCATTCCCTCCACAGAACTGGCCAAACAGGTCATCGAGTATGCCCGGC GAAGCCGGAAGACACCACCATTCCCTCCACAGTACTGGCCAAACAGGTCATCGAGTATGCCCGGC A T PSMD8 Ensembl:ENSG00000099341 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 THCA 1 - Human_RBP_ID_521107,Human_RBP_ID_773448,Human_RBP_ID_1015648,Human_RBP_ID_1563885,Human_RBP_ID_2564913,Human_RBP_ID_17268857,Human_RBP_ID_17383958,Human_RBP_ID_17499789,Human_RBP_ID_18532433,Human_RBP_ID_22234465,Human_RBP_ID_22448662,Human_RBP_ID_26815770,Human_RBP_ID_26989312,Human_RBP_ID_27273729 Human_Splice_Rec_2001632,Human_Splice_Rec_2001644,Human_Splice_Rec_2001660,Human_Splice_Rec_2001704 111426 RMVar_ID_111426 Human_SNP_ID_832766520 m1A Human chr19 + 1854558 1854558 1854558 AGCGAGTCGCTGGGGGAGGTACTGCGGGCACCAGGGCGCCGGAGCAGGTCCGGGTGGAAGCCGGG AGCGAGTCGCTGGGGGAGGTACTGCGGGCACCGGGGCGCCGGAGCAGGTCCGGGTGGAAGCCGGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1854324..1854665 26863196 MeRIP-seq:(Medium) rs3746045 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,COCA,large_intestine adenocarcinoma 16 caecum,head and neck,large intestine 111427 RMVar_ID_111427 Human_SNP_ID_832772101 m1A Human chr19 - 49679848 49679847 49679848 TACAAAATTCTAGGAGAGAGTAACAGGGAAAAAGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC TACAAAATTCTAGGAGAGAGTAACAGGGAAAA_GGATTAGCTACTGGGAGTGGCTGTGGGAGGGC CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49679845..49679995;chr19:49679845..49679953 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 BRCA 1 - 111428 RMVar_ID_111428 Human_SNP_ID_832772183 m1A Human chr19 + 14563251 14563251 14563251 CCACCATTGCGGAGATCAAGAACCTCTTCACTAAGACCCGTGAGTTCTAGTCCCGGCCACACTGC CCACCATTGCGGAGATCAAGAACCTCTTCACTGAGACCCGTGAGTTCTAGTCCCGGCCACACTGC A G TECR Ensembl:ENSG00000099797 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14562120..14563289 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_5116758,Human_RBP_ID_18421557 Human_Splice_Rec_1968978,Human_Splice_Rec_1968979,Human_Splice_Rec_1968988,Human_Splice_Rec_1968989,Human_Splice_Rec_1969004,Human_Splice_Rec_1969005,Human_Splice_Rec_1969028,Human_Splice_Rec_1969029,Human_Splice_Rec_1969053,Human_Splice_Rec_1969078,Human_Splice_Rec_1969079,Human_Splice_Rec_1969106,Human_Splice_Rec_1969107,Human_Splice_Rec_1969120,Human_Splice_Rec_1969121,Human_Splice_Rec_1969128,Human_Splice_Rec_1969129,Human_Splice_Rec_1969150,Human_Splice_Rec_1969151,Human_Splice_Rec_1969164,Human_Splice_Rec_1969165,Human_Splice_Rec_1969186,Human_Splice_Rec_1969187,Human_Splice_Rec_1969194,Human_Splice_Rec_1969195,Human_Splice_Rec_1969204,Human_Splice_Rec_1969205,Human_Splice_Rec_1969212,Human_Splice_Rec_1969213,Human_Splice_Rec_1969228,Human_Splice_Rec_1969229,Human_Splice_Rec_1969240,Human_Splice_Rec_1969241 RMVar_hsa_circ_1359,RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_96663,RMVar_hsa_circ_193035,RMVar_hsa_circ_7801,RMVar_hsa_circ_7258,RMVar_hsa_circ_193037 111429 RMVar_ID_111429 Human_SNP_ID_832775466 m1A Human chr19 + 48382749 48382748 48382749 CAGGAGAAGACCAAAAAATTCAAACTCTGGGGAAAAAAATTACTATGAAAAAAAATCAGGGGAGA CAGGAGAAGACCAAAAAATTCAAACTCTGGGG_AAAAAATTACTATGAAAAAAAATCAGGGGAGA GA G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:48382699..48382937 26863196 MeRIP-seq:(Medium) rs889036713 Functional Loss DEL ICGC 33..33 33 ESCA 1 - 111430 RMVar_ID_111430 Human_SNP_ID_832776524 m1A Human chr19 - 38840228 38840228 38840228 AGTCGCTACGGCCCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCA AGTCGCTACGGCCCCCAGTATGGGCACCCCCCCCCCCCTCCCCCACCACCCGAGTATGGCCCTCA T G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs757247424 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,central_nervous_system astrocytoma_Grade_IV,lung adenocarcinoma,head_neck squamous_cell_carcinoma,brain astrocytoma_Grade_IV,CHOL,right_upper_lobe adenocarcinoma,liver hepatocellular_carcinoma 23 lung,liver,head and neck,brain Human_miRNA_ID_1560578,Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 111431 RMVar_ID_111431 Human_SNP_ID_832777222 m1A Human chr19 - 879659 879659 879659 GCACGTGGGGCTGGGGCTGGTGGGCATTGACAACCAGGGGAACGTGAGCTGCTGGGGCACGTGGG GCACGTGGGGCTGGGGCTGGTGGGCATTGACAGCCAGGGGAACGTGAGCTGCTGGGGCACGTGGG T C MED16 Ensembl:ENSG00000175221 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:879656..879808 26863196 MeRIP-seq:(Medium) rs28414042 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,PBCA,skin mycosis_fungoides-Sezary_syndrome 8 skin,haematopoietic and lymphoid tissue Human_RBP_ID_5320694 RMVar_hsa_circ_94288,RMVar_hsa_circ_190923 111432 RMVar_ID_111432 Human_SNP_ID_832779157 m1A Human chr19 - 18531829 18531829 18531829 CTGCCTAGTCCCCGCCTGAGTGCCAGCCCCCCACCCCGCCTGCCGCCCCCTGTCCAGGTTCCCTC CTGCCTAGTCCCCGCCTGAGTGCCAGCCCCCCCCCCCGCCTGCCGCCCCCTGTCCAGGTTCCCTC T G FKBP8 Ensembl:ENSG00000105701 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs867183065 Functional Loss SNV ICGC 33..33 33 MALY 2 - Human_RBP_ID_516263,Human_RBP_ID_4510671,Human_RBP_ID_9328827,Human_RBP_ID_17082378,Human_RBP_ID_17387309,Human_RBP_ID_17568512,Human_RBP_ID_18945241 Human_miRNA_ID_1703573 111433 RMVar_ID_111433 Human_SNP_ID_832779323 m1A Human chr19 - 45396978 45396978 45396978 GGGTCCCCCCGGAAGGCGGCCACCGACGGCGCAGACACCCCGTTCGGACGATCAGAGAGTGCCCC GGGTCCCCCCGGAAGGCGGCCACCGACGGCGCTGACACCCCGTTCGGACGATCAGAGAGTGCCCC T A PPP1R13L Ensembl:ENSG00000104881 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:45396526..45398075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 8 liver Human_Splice_Rec_2019284,Human_Splice_Rec_2019308,Human_Splice_Rec_2019336,Human_Splice_Rec_2019350 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 111434 RMVar_ID_111434 Human_SNP_ID_832780558 m1A Human chr19 - 2339959 2339959 2339959 GGCCCACCCGCCCGGGGCCGCGCACCGAGGAGATCGTAGAAATAGTAGAGCAGCACCAGCATGGA GGCCCACCCGCCCGGGGCCGCGCACCGAGGAGGTCGTAGAAATAGTAGAGCAGCACCAGCATGGA T C lnc-LSM7-3 RNACentral:URS00008B59FE lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:2339940..2340066 26863196 MeRIP-seq:(Medium) rs1609752 Functional Loss SNV ICGC 33..33 33 COCA 5 - 111435 RMVar_ID_111435 Human_SNP_ID_832783015 m1A Human chr19 - 39386352 39386352 39386352 CAGCAGCAGTGAGAAGGAGGGCAGTGAAGATGAGCACTCGGGCAGCGAGAGTGAACGGGAGGAAG CAGCAGCAGTGAGAAGGAGGGCAGTGAAGATGGGCACTCGGGCAGCGAGAGTGAACGGGAGGAAG T C PAF1 Ensembl:ENSG00000006712 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:39386076..39386775;chr19:39386051..39386803;chr19:39385936..39388700;chr19:39386051..39386800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach Human_RBP_ID_823870,Human_RBP_ID_1015930,Human_RBP_ID_3954994,Human_RBP_ID_4527459,Human_RBP_ID_6761538,Human_RBP_ID_13453461,Human_RBP_ID_23797027,Human_RBP_ID_24545478,Human_RBP_ID_26336242 Human_Splice_Rec_2005486 RMVar_hsa_circ_96937,RMVar_hsa_circ_194731,RMVar_hsa_circ_93122,RMVar_hsa_circ_194730 111436 RMVar_ID_111436 Human_SNP_ID_832783480 m1A Human chr19 + 37792613 37792613 37792613 TATCCATCTCAGATACCAGCAACTCCCCCATCATATGAATCTGTAGATGACATTAATGCTGATAA TATCCATCTCAGATACCAGCAACTCCCCCATCGTATGAATCTGTAGATGACATTAATGCTGATAA A G AC016582.2 Ensembl:ENSG00000267422 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879202738 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_23796028 111437 RMVar_ID_111437 Human_SNP_ID_832793312 m1A Human chr19 + 55695306 55695306 55695306 CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCATGATGCCCCCGGGCCCCCCGGCCCCCAACACT CTCCCCTTGGCGGGGGCCCTGGCCTGCCCCCCCTGATGCCCCCGGGCCCCCCGGCCCCCAACACT A C EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:55695106..55695725 26863196 MeRIP-seq:(Medium) rs755464988 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_527293,Human_RBP_ID_4548250,Human_RBP_ID_17387062,Human_RBP_ID_17657381,Human_RBP_ID_18192518,Human_RBP_ID_18947391,Human_RBP_ID_22976225 Human_miRNA_ID_2277236 RMVar_hsa_circ_100870,RMVar_hsa_circ_196367 111438 RMVar_ID_111438 Human_SNP_ID_832796133 m1A Human chr19 + 7559015 7559015 7559015 GGCTGACAAGGTAAAGGTTCCAGACATGGCTGAAATCCAGTCCCGCCTGGCCTACGTGTCCTGTG GGCTGACAAGGTAAAGGTTCCAGACATGGCTGTAATCCAGTCCCGCCTGGCCTACGTGTCCTGTG A T PNPLA6 Ensembl:ENSG00000032444 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7558964..7559114 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_529298 Human_miRNA_ID_2378673,Human_miRNA_ID_3093743 RMVar_hsa_circ_94926,RMVar_hsa_circ_191995,RMVar_hsa_circ_191997,RMVar_hsa_circ_116972 111439 RMVar_ID_111439 Human_SNP_ID_832797621 m1A Human chr19 + 757412 757412 757412 CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCAGCACCGTGGCCACGCTCCAGGGCACTCCTGAC CCGTCATCCAGGGCCAGGCAGTCAGGAAGAGCGGCACCGTGGCCACGCTCCAGGGCACTCCTGAC A G MISP Ensembl:ENSG00000099812 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:757150..757614 26863196 MeRIP-seq:(Medium) rs3746173 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,mouth squamous_cell_carcinoma,liver hepatocellular_carcinoma 5 liver,head and neck RMVar_hsa_circ_314961 111440 RMVar_ID_111440 Human_SNP_ID_832798051 m1A Human chr19 + 18168527 18168527 18168527 CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGATTAAAAATGAGACTGAGGAGTGAGTGACCGTC CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGCTTAAAAATGAGACTGAGGAGTGAGTGACCGTC A C PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18168439..18168582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 2 head and neck Human_Splice_Rec_1979306,Human_Splice_Rec_1979307,Human_Splice_Rec_1979354,Human_Splice_Rec_1979355,Human_Splice_Rec_1979382,Human_Splice_Rec_1979383,Human_Splice_Rec_1979430,Human_Splice_Rec_1979431,Human_Splice_Rec_1979450,Human_Splice_Rec_1979451,Human_Splice_Rec_1979456,Human_Splice_Rec_1979457 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445 111441 RMVar_ID_111441 Human_SNP_ID_832798068 m1A Human chr19 + 18168527 18168527 18168527 CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGATTAAAAATGAGACTGAGGAGTGAGTGACCGTC CCCGGCAGAAGAAAATCAACGAGTGGCTGGGGGTTAAAAATGAGACTGAGGAGTGAGTGACCGTC A G PIK3R2,AC007192.1 Ensembl:ENSG00000105647,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18168439..18168582 26863196 MeRIP-seq:(Medium) rs767446008 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_Splice_Rec_1979306,Human_Splice_Rec_1979307,Human_Splice_Rec_1979354,Human_Splice_Rec_1979355,Human_Splice_Rec_1979382,Human_Splice_Rec_1979383,Human_Splice_Rec_1979430,Human_Splice_Rec_1979431,Human_Splice_Rec_1979450,Human_Splice_Rec_1979451,Human_Splice_Rec_1979456,Human_Splice_Rec_1979457 RMVar_hsa_circ_78293,RMVar_hsa_circ_103306,RMVar_hsa_circ_78260,RMVar_hsa_circ_193435,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_84194,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193439,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445 111442 RMVar_ID_111442 Human_SNP_ID_832800241 m1A Human chr19 - 4099163 4099163 4099163 GCCTGAATCTGCAACTTCCGGTCTGGACGCGCAGTGCCCTGCGCGGGGCCTGCTGTGCCAGGGTC GCCTGAATCTGCAACTTCCGGTCTGGACGCGCGGTGCCCTGCGCGGGGCCTGCTGTGCCAGGGTC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4099162..4099399 26863196 MeRIP-seq:(Medium) rs760344244 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 111443 RMVar_ID_111443 Human_SNP_ID_832800536 m1A Human chr19 + 49596754 49596754 49596754 CGCCTCCCCCCCAGCTGCTCCCCTCGGTCCTCAGCCATGCCCCCAGTCCCTCTCCCAGCGCCTCC CGCCTCCCCCCCAGCTGCTCCCCTCGGTCCTCCGCCATGCCCCCAGTCCCTCTCCCAGCGCCTCC A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49596706..49596828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_18945839,Human_RBP_ID_22072058,Human_RBP_ID_27470362 Human_miRNA_ID_1962835,Human_miRNA_ID_2352273,Human_miRNA_ID_2494002,Human_miRNA_ID_3047818 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111444 RMVar_ID_111444 Human_SNP_ID_832803419 m1A Human chr19 + 38383350 38383350 38383350 CACCACCATTCCCTCCACAGAACTGGCCAAACAGGTCATCGAGTATGCCCGGCAGCTGGAGATGA CACCACCATTCCCTCCACAGAACTGGCCAAACTGGTCATCGAGTATGCCCGGCAGCTGGAGATGA A T PSMD8 Ensembl:ENSG00000099341 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38383300..38383382 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 5 lung Human_RBP_ID_521107,Human_RBP_ID_1015648,Human_RBP_ID_1563886,Human_RBP_ID_1886947,Human_RBP_ID_9380959,Human_RBP_ID_17271848,Human_RBP_ID_17655345,Human_RBP_ID_22448662,Human_RBP_ID_26815770 Human_Splice_Rec_2001632,Human_Splice_Rec_2001644,Human_Splice_Rec_2001660,Human_Splice_Rec_2001704 111445 RMVar_ID_111445 Human_SNP_ID_832804368 m1A Human chr19 + 1429993 1429993 1429993 ATCTAGGAATGTGGGTGCCGGCAGGACAGGCGATTGGTAAGTCCTTGTTTATAGAGCAAAGGCGG ATCTAGGAATGTGGGTGCCGGCAGGACAGGCGGTTGGTAAGTCCTTGTTTATAGAGCAAAGGCGG A G DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1428823..1432106 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 WT 1 - Human_RBP_ID_514241,Human_RBP_ID_908225,Human_RBP_ID_5372545,Human_RBP_ID_8101450,Human_RBP_ID_18165898,Human_RBP_ID_19088448,Human_RBP_ID_22370999,Human_RBP_ID_22661531 Human_Splice_Rec_1932442,Human_Splice_Rec_1932443,Human_Splice_Rec_1932466,Human_Splice_Rec_1932467,Human_Splice_Rec_1932488,Human_Splice_Rec_1932489,Human_Splice_Rec_1932522,Human_Splice_Rec_1932523,Human_Splice_Rec_1932542,Human_Splice_Rec_1932543,Human_Splice_Rec_1932572,Human_Splice_Rec_1932573,Human_Splice_Rec_1932580,Human_Splice_Rec_1932581 RMVar_hsa_circ_56402,RMVar_hsa_circ_101096,RMVar_hsa_circ_294232,RMVar_hsa_circ_374085,RMVar_hsa_circ_191053,RMVar_hsa_circ_60808,RMVar_hsa_circ_191054,RMVar_hsa_circ_191055,RMVar_hsa_circ_191062,RMVar_hsa_circ_77574,RMVar_hsa_circ_126606,RMVar_hsa_circ_98670,RMVar_hsa_circ_57492,RMVar_hsa_circ_191063,RMVar_hsa_circ_125272,RMVar_hsa_circ_191064,RMVar_hsa_circ_76519,RMVar_hsa_circ_93413,RMVar_hsa_circ_191065,RMVar_hsa_circ_191066,RMVar_hsa_circ_108515,RMVar_hsa_circ_191067,RMVar_hsa_circ_191068 111446 RMVar_ID_111446 Human_SNP_ID_832807232 m1A Human chr19 - 38736816 38736811 38736816 GGACAGACAGAGGGACGAGGTTAGGGACAGAGAGAGGCTGGGGGTTAGAAGGGCCAGAGGGGACC GGACAGACAGAGGGACGAGGTTAGGGACAGAG_____CTGGGGGTTAGAAGGGCCAGAGGGGACC GCCTCT G CAPN12 Ensembl:ENSG00000182472 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38736671..38736970 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..37 33 SKCA 1 - Human_RBP_ID_3581176,Human_RBP_ID_5320347,Human_RBP_ID_8196449,Human_RBP_ID_8942214,Human_RBP_ID_9425310,Human_RBP_ID_9929733,Human_RBP_ID_18421371,Human_RBP_ID_21979232,Human_RBP_ID_26472467 111447 RMVar_ID_111447 Human_SNP_ID_832808142 m1A Human chr19 - 10489743 10489743 10489743 CAATCGTCTCCTTTATGCCGTGGGGGGCTTTGACGGGACAAACCGCCTTAATTCAGCTGAGTGTT CAATCGTCTCCTTTATGCCGTGGGGGGCTTTGGCGGGACAAACCGCCTTAATTCAGCTGAGTGTT T C KEAP1 Ensembl:ENSG00000079999 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:10489651..10489800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_17914236 Human_Splice_Rec_1954867,Human_Splice_Rec_1954875,Human_Splice_Rec_1954885 RMVar_hsa_circ_192369,RMVar_hsa_circ_291691,RMVar_hsa_circ_306319,RMVar_hsa_circ_192370,RMVar_hsa_circ_192371,RMVar_hsa_circ_368444 111448 RMVar_ID_111448 Human_SNP_ID_832812598 m1A Human chr19 - 48150209 48150209 48150209 TTGCATCACCGTCTGAGCTCTCTCACCGCAGAAGCAGAGACCCCGACGGAAAGCGTTTCAGAGCC TTGCATCACCGTCTGAGCTCTCTCACCGCAGACGCAGAGACCCCGACGGAAAGCGTTTCAGAGCC T G LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:48150159..48150307 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_Splice_Rec_2025188,Human_Splice_Rec_2025238,Human_Splice_Rec_2025294,Human_Splice_Rec_2025344,Human_Splice_Rec_2025388,Human_Splice_Rec_2025440,Human_Splice_Rec_2025492,Human_Splice_Rec_2025572,Human_Splice_Rec_2025590,Human_Splice_Rec_2025598,Human_Splice_Rec_2025606,Human_Splice_Rec_2025616 RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_376509,RMVar_hsa_circ_119674,RMVar_hsa_circ_95771,RMVar_hsa_circ_103030,RMVar_hsa_circ_86212,RMVar_hsa_circ_4035,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,RMVar_hsa_circ_195644,RMVar_hsa_circ_195643,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652,RMVar_hsa_circ_3893,RMVar_hsa_circ_48843,RMVar_hsa_circ_34463,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_83444,RMVar_hsa_circ_195654,RMVar_hsa_circ_295820,RMVar_hsa_circ_304632,RMVar_hsa_circ_317913,RMVar_hsa_circ_62852,RMVar_hsa_circ_195655,RMVar_hsa_circ_195656,RMVar_hsa_circ_195657 111449 RMVar_ID_111449 Human_SNP_ID_832814835 m1A Human chr19 + 41305744 41305744 41305744 TACAGCCAGGGCTACACAGCCCCACCGCCTCCACCTCCACCACCACCTGCCTACAACTATGGGAG TACAGCCAGGGCTACACAGCCCCACCGCCTCCGCCTCCACCACCACCTGCCTACAACTATGGGAG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:41305658..41305797 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5131253,Human_RBP_ID_6766023,Human_RBP_ID_17269420,Human_RBP_ID_17384386,Human_RBP_ID_17500392 Human_Splice_Rec_2010792,Human_Splice_Rec_2010820,Human_Splice_Rec_2010880,Human_Splice_Rec_2010908,Human_Splice_Rec_2010936,Human_Splice_Rec_2010942,Human_Splice_Rec_2011006,Human_Splice_Rec_2011046,Human_Splice_Rec_2011090 Human_miRNA_ID_1016721,Human_miRNA_ID_1302993 RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 111450 RMVar_ID_111450 Human_SNP_ID_832815258 m1A Human chr19 + 13972896 13972896 13972896 CCCCCGCCACCGCCTCCCCCGCCGCCGCCGCCACCACCACTGCCACCACCTCCGCTGCTGTTGCT CCCCCGCCACCGCCTCCCCCGCCGCCGCCGCCGCCACCACTGCCACCACCTCCGCTGCTGTTGCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:13972859..13972980 26863196 MeRIP-seq:(Medium) rs766666783 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 4 uterus,large intestine 111451 RMVar_ID_111451 Human_SNP_ID_832815470 m1A Human chr19 - 49679848 49679848 49679848 TACAAAATTCTAGGAGAGAGTAACAGGGAAAAAGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC TACAAAATTCTAGGAGAGAGTAACAGGGAAAAGGGATTAGCTACTGGGAGTGGCTGTGGGAGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49679845..49679995;chr19:49679845..49679953 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 111452 RMVar_ID_111452 Human_SNP_ID_832816499 m1A Human chr19 + 14471650 14471650 14471650 CACCGCCCTTTGTGCCCACGCTGTCCGGCCGCACCGACGTCAGCAACTTCGACGAGGAGTTCACC CACCGCCCTTTGTGCCCACGCTGTCCGGCCGCGCCGACGTCAGCAACTTCGACGAGGAGTTCACC A G PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:14471576..14471800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_514375,Human_RBP_ID_8478261,Human_RBP_ID_9293471,Human_RBP_ID_18192065,Human_RBP_ID_18412305 Human_Splice_Rec_1968674,Human_Splice_Rec_1968710,Human_Splice_Rec_1968780,Human_Splice_Rec_1968798,Human_Splice_Rec_1968818,Human_Splice_Rec_1968822,Human_Splice_Rec_1968826 111453 RMVar_ID_111453 Human_SNP_ID_832820854 m1A Human chr19 - 35733869 35733869 35733869 AGGAGGGAGAGGGCAAGGCCGGTCCCTACCTGAATAGTGGTGCCACTGGGACTCAAGCAGCAGGT AGGAGGGAGAGGGCAAGGCCGGTCCCTACCTGGATAGTGGTGCCACTGGGACTCAAGCAGCAGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35733634..35735257 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111454 RMVar_ID_111454 Human_SNP_ID_832824284 m1A Human chr19 + 46978705 46978705 46978705 GTTTGTGTGGTGGGATGTGTGTGTGGTGGGGCATGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC GTTTGTGTGGTGGGATGTGTGTGTGGTGGGGCGTGTGTGTGGTGGGATGTGTGTGTGGTGGAGTC A G ARHGAP35 Ensembl:ENSG00000160007 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46978695..46978760 26863196 MeRIP-seq:(Medium) rs987870909 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_3583836,Human_RBP_ID_5293018,Human_RBP_ID_5650264,Human_RBP_ID_8103123,Human_RBP_ID_8196695,Human_RBP_ID_8233179,Human_RBP_ID_17272442,Human_RBP_ID_21979318 111455 RMVar_ID_111455 Human_SNP_ID_832826148 m1A Human chr19 - 531836 531836 531836 AGACGGGCCGGGCCGCGCACCGTCCGGGGGGGAGCCACCGGGGCCGCCGCCTGCCTCCTCCTCTG AGACGGGCCGGGCCGCGCACCGTCCGGGGGGGGGCCACCGGGGCCGCCGCCTGCCTCCTCCTCTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:531738..532025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111456 RMVar_ID_111456 Human_SNP_ID_832827796 m1A Human chr19 - 39388669 39388669 39388669 TTGCTACTCCTTTTCCCCCAACCAGGGGCATGATGGATGAGGAAGGGAACCAGTTTGTGGCCTAT TTGCTACTCCTTTTCCCCCAACCAGGGGCATGGTGGATGAGGAAGGGAACCAGTTTGTGGCCTAT T C PAF1 Ensembl:ENSG00000006712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39388541..39388675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_8833898,Human_RBP_ID_13453490,Human_RBP_ID_18997753,Human_RBP_ID_22972440 Human_Splice_Rec_2005478,Human_Splice_Rec_2005502,Human_Splice_Rec_2005528 Human_miRNA_ID_2959464 RMVar_hsa_circ_12555,RMVar_hsa_circ_96937,RMVar_hsa_circ_194731,RMVar_hsa_circ_93122,RMVar_hsa_circ_194730,RMVar_hsa_circ_69767 111457 RMVar_ID_111457 Human_SNP_ID_832828030 m1A Human chr19 + 808411 808411 808411 GCGCGTGAAGATCCTGTTCAATAAGAAGGAGAACGCCCTAGTGCAGATGGCGGACGGCAACCAGG GCGCGTGAAGATCCTGTTCAATAAGAAGGAGAGCGCCCTAGTGCAGATGGCGGACGGCAACCAGG A G PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:808329..808468 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 6 skin,head and neck Human_RBP_ID_529577,Human_RBP_ID_4555324,Human_RBP_ID_5585982,Human_RBP_ID_13535146,Human_RBP_ID_17271438,Human_RBP_ID_18995572,Human_RBP_ID_22590330,Human_RBP_ID_23811655 Human_Splice_Rec_1928968,Human_Splice_Rec_1928969,Human_Splice_Rec_1928980,Human_Splice_Rec_1928981,Human_Splice_Rec_1929014,Human_Splice_Rec_1929015,Human_Splice_Rec_1929044,Human_Splice_Rec_1929045,Human_Splice_Rec_1929072,Human_Splice_Rec_1929073,Human_Splice_Rec_1929100,Human_Splice_Rec_1929101,Human_Splice_Rec_1929124,Human_Splice_Rec_1929125,Human_Splice_Rec_1929152,Human_Splice_Rec_1929153,Human_Splice_Rec_1929180,Human_Splice_Rec_1929181,Human_Splice_Rec_1929196,Human_Splice_Rec_1929197,Human_Splice_Rec_1929210,Human_Splice_Rec_1929211,Human_Splice_Rec_1929219 RMVar_hsa_circ_24441,RMVar_hsa_circ_361069,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_93785,RMVar_hsa_circ_96776,RMVar_hsa_circ_190908,RMVar_hsa_circ_190912,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_89521,RMVar_hsa_circ_190917,RMVar_hsa_circ_926,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 111458 RMVar_ID_111458 Human_SNP_ID_832835607 m1A Human chr19 + 14562574 14562574 14562574 AAAGACAAGGGAGAAGCTGTGTTTCTTGGACAAGGTAGGACTGGGGCGTGGGCTGCACTGGGCCA AAAGACAAGGGAGAAGCTGTGTTTCTTGGACATGGTAGGACTGGGGCGTGGGCTGCACTGGGCCA A T TECR Ensembl:ENSG00000099797 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Normoxia chr19:14562120..14563275;chr19:14562120..14563189 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_238912,Human_RBP_ID_825825,Human_RBP_ID_5116756,Human_RBP_ID_17655990,Human_RBP_ID_18421644,Human_RBP_ID_22447494 Human_Splice_Rec_1968976,Human_Splice_Rec_1968977,Human_Splice_Rec_1968986,Human_Splice_Rec_1968987,Human_Splice_Rec_1969002,Human_Splice_Rec_1969003,Human_Splice_Rec_1969026,Human_Splice_Rec_1969027,Human_Splice_Rec_1969050,Human_Splice_Rec_1969051,Human_Splice_Rec_1969076,Human_Splice_Rec_1969077,Human_Splice_Rec_1969100,Human_Splice_Rec_1969101,Human_Splice_Rec_1969104,Human_Splice_Rec_1969105,Human_Splice_Rec_1969118,Human_Splice_Rec_1969119,Human_Splice_Rec_1969126,Human_Splice_Rec_1969127,Human_Splice_Rec_1969148,Human_Splice_Rec_1969149,Human_Splice_Rec_1969162,Human_Splice_Rec_1969163,Human_Splice_Rec_1969184,Human_Splice_Rec_1969185,Human_Splice_Rec_1969192,Human_Splice_Rec_1969193,Human_Splice_Rec_1969202,Human_Splice_Rec_1969203,Human_Splice_Rec_1969210,Human_Splice_Rec_1969211,Human_Splice_Rec_1969226,Human_Splice_Rec_1969227,Human_Splice_Rec_1969239 RMVar_hsa_circ_1359,RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_93654,RMVar_hsa_circ_96663,RMVar_hsa_circ_193035,RMVar_hsa_circ_7801,RMVar_hsa_circ_193036,RMVar_hsa_circ_193037 111459 RMVar_ID_111459 Human_SNP_ID_832839012 m1A Human chr19 - 12838527 12838527 12838527 CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGAGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG CGACATGGTGGCAGGTGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGCGGGGAGCAAGCG T G HOOK2 Ensembl:ENSG00000095066 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12838512..12838620 26863196 MeRIP-seq:(Medium) rs746538311 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 111460 RMVar_ID_111460 Human_SNP_ID_832840725 m1A Human chr19 - 17232423 17232423 17232423 TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCATTGAGACACTGATCAGAGACATGCTGCTGTCG TGTTCTTCATGCGCCTGGTGGGGAAGACGCCCGTTGAGACACTGATCAGAGACATGCTGCTGTCG T C NR2F6 Ensembl:ENSG00000160113 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:17232376..17232575 26863196 MeRIP-seq:(Medium) rs765130843 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_54286,Human_RBP_ID_515577,Human_RBP_ID_1881066,Human_RBP_ID_4563523,Human_RBP_ID_8839204,Human_RBP_ID_9293516,Human_RBP_ID_13390884,Human_RBP_ID_17916809,Human_RBP_ID_18440730,Human_RBP_ID_22071011,Human_RBP_ID_26984938,Human_RBP_ID_27269735 Human_miRNA_ID_2769358 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_94273,RMVar_hsa_circ_193286,RMVar_hsa_circ_193284 111461 RMVar_ID_111461 Human_SNP_ID_832841302 m1A Human chr19 - 49491847 49491847 49491847 CATTCCAGGGCAACAATGGAGGAAGGGCAGGCAACGCATGAGGAATTAACAGTCTTTATTGGGCT CATTCCAGGGCAACAATGGAGGAAGGGCAGGCCACGCATGAGGAATTAACAGTCTTTATTGGGCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr19:49491776..49492210;chr19:49491776..49492188;chr19:49491776..49492219;chr19:49491799..49492218;chr19:49491740..49491919 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 111462 RMVar_ID_111462 Human_SNP_ID_832844704 m1A Human chr19 - 54146008 54146008 54146008 GGTACAGTTGGCTGGGCTGGGCGGGATGGGAGAGCTGGAGGTGGTTGAGGTGGGCGTGCTGCTGG GGTACAGTTGGCTGGGCTGGGCGGGATGGGAGGGCTGGAGGTGGTTGAGGTGGGCGTGCTGCTGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54145958..54146073 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 4 head and neck 111463 RMVar_ID_111463 Human_SNP_ID_832847025 m1A Human chr19 - 18900435 18900435 18900435 GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCAGAGACGCTGGTCAACCTCATCGTCCTGTCCCA GTCTGCCTGTGTCTCCAGGATAGTGGCTACCCGGAGACGCTGGTCAACCTCATCGTCCTGTCCCA T C COPE Ensembl:ENSG00000105669 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18899957..18903468 26863196 MeRIP-seq:(Medium) rs1127821 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 17 lung,head and neck,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_53434,Human_RBP_ID_22476571,Human_RBP_ID_22762897 Human_Splice_Rec_1981398,Human_Splice_Rec_1981399,Human_Splice_Rec_1981414,Human_Splice_Rec_1981415,Human_Splice_Rec_1981420,Human_Splice_Rec_1981421,Human_Splice_Rec_1981440,Human_Splice_Rec_1981441,Human_Splice_Rec_1981454,Human_Splice_Rec_1981455,Human_Splice_Rec_1981470,Human_Splice_Rec_1981471,Human_Splice_Rec_1981482,Human_Splice_Rec_1981483 GWAS_ID_6631 RMVar_hsa_circ_193546,RMVar_hsa_circ_109918,RMVar_hsa_circ_86189,RMVar_hsa_circ_96801,RMVar_hsa_circ_193545,RMVar_hsa_circ_344320,RMVar_hsa_circ_193547,RMVar_hsa_circ_62378 111464 RMVar_ID_111464 Human_SNP_ID_832847720 m1A Human chr19 - 40576962 40576962 40576962 CACACTCACCTCTTGCCTCCCACATTCAGATGAATGACTTCCCCGGGAGGCCCCCGACTGGGGAC CACACTCACCTCTTGCCTCCCACATTCAGATGGATGACTTCCCCGGGAGGCCCCCGACTGGGGAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40576912..40577014 26863196 MeRIP-seq:(Medium) rs16974365 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue GWAS_ID_10111 111465 RMVar_ID_111465 Human_SNP_ID_832848015 m1A Human chr19 - 406485 406485 406485 TCCCAGGCTCCGGTGGGGAGTGGGGCCAGGCGAGGGTGCCCTGACGAGGGTGGGCGCGGAGGGAG TCCCAGGCTCCGGTGGGGAGTGGGGCCAGGCGGGGGTGCCCTGACGAGGGTGGGCGCGGAGGGAG T C C2CD4C Ensembl:ENSG00000183186 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:406231..406580 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111466 RMVar_ID_111466 Human_SNP_ID_832857817 m1A Human chr19 + 44812516 44812516 44812516 CAGAGGCCACTGAGGTCTCCCCCAACAAAGGGACACTGTCTGTGATGGAGGACTCTGCCCAGGAG CAGAGGCCACTGAGGTCTCCCCCAACAAAGGGGCACTGTCTGTGATGGAGGACTCTGCCCAGGAG A G BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:44812187..44812572 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain Human_RBP_ID_18998038 Human_Splice_Rec_2017706,Human_Splice_Rec_2017707,Human_Splice_Rec_2017732,Human_Splice_Rec_2017733,Human_Splice_Rec_2017762,Human_Splice_Rec_2017763,Human_Splice_Rec_2017774 111467 RMVar_ID_111467 Human_SNP_ID_832858879 m1A Human chr19 - 12801261 12801261 12801261 CACTGACCGGGCGGGGGTCTCAGCTTTCAGTCATGGCCTCCGGTAACGCGCGCATCGGAAAGCCA CACTGACCGGGCGGGGGTCTCAGCTTTCAGTCTTGGCCTCCGGTAACGCGCGCATCGGAAAGCCA T A PRDX2,HOOK2 Ensembl:ENSG00000167815,Ensembl:ENSG00000095066 Protein coding,Protein coding start codon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12801210..12801305 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_54500,Human_RBP_ID_772019,Human_RBP_ID_914496,Human_RBP_ID_1554751,Human_RBP_ID_4558115,Human_RBP_ID_5320180,Human_RBP_ID_9328657,Human_RBP_ID_18192010,Human_RBP_ID_22448422 Human_Splice_Rec_1963592,Human_Splice_Rec_1963600,Human_Splice_Rec_1963606,Human_Splice_Rec_1963620 RMVar_hsa_circ_115238,RMVar_hsa_circ_112810,RMVar_hsa_circ_192788,RMVar_hsa_circ_192787,RMVar_hsa_circ_331336,RMVar_hsa_circ_192794 111468 RMVar_ID_111468 Human_SNP_ID_832860868 m1A Human chr19 + 55678773 55678773 55678773 CCTCATGTCAGAGATTGCCGACCTCACCTACAACGTTGTCGCCTTCTCGGAGATCATGAGCATGA CCTCATGTCAGAGATTGCCGACCTCACCTACAGCGTTGTCGCCTTCTCGGAGATCATGAGCATGA A G EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:55678526..55678850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_52604,Human_RBP_ID_4548177,Human_RBP_ID_8840249,Human_RBP_ID_26816344,Human_RBP_ID_27471583 Human_Splice_Rec_2048015,Human_Splice_Rec_2048035,Human_Splice_Rec_2048055 RMVar_hsa_circ_89787,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196363,RMVar_hsa_circ_332992,RMVar_hsa_circ_196364,RMVar_hsa_circ_196365 111469 RMVar_ID_111469 Human_SNP_ID_832861560 m1A Human chr19 + 39370055 39370055 39370055 GGCTGGCAGGACAAGCCACCCCGGGAAAATGGACACGTGCCCTTCCACCCATCCAGCTCAGTGCC GGCTGGCAGGACAAGCCACCCCGGGAAAATGGGCACGTGCCCTTCCACCCATCCAGCTCAGTGCC A G SAMD4B Ensembl:ENSG00000179134 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39370004..39370150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_8833856,Human_RBP_ID_17924442,Human_RBP_ID_20349394,Human_RBP_ID_26468084,Human_RBP_ID_27274074 Human_Splice_Rec_2005341,Human_Splice_Rec_2005371,Human_Splice_Rec_2005397,Human_Splice_Rec_2005419,Human_Splice_Rec_2005443,Human_Splice_Rec_2005447,Human_Splice_Rec_2005449 RMVar_hsa_circ_2889,RMVar_hsa_circ_333351,RMVar_hsa_circ_310231,RMVar_hsa_circ_49018,RMVar_hsa_circ_93073,RMVar_hsa_circ_22957,RMVar_hsa_circ_40388,RMVar_hsa_circ_338453,RMVar_hsa_circ_194721,RMVar_hsa_circ_65374,RMVar_hsa_circ_76727,RMVar_hsa_circ_194722 111470 RMVar_ID_111470 Human_SNP_ID_832861810 m1A Human chr19 + 7921523 7921523 7921523 TGGCCTTCAGGGACCAAGGCGCCGGGAGGCACAGCCCCCAGCCCCCATAGAGGTGAGGCAGATGA TGGCCTTCAGGGACCAAGGCGCCGGGAGGCACGGCCCCCAGCCCCCATAGAGGTGAGGCAGATGA A G SNAPC2 Ensembl:ENSG00000104976 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7921477..7922151 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 4 lung Human_Splice_Rec_1948873,Human_Splice_Rec_1948881,Human_Splice_Rec_1948887,Human_Splice_Rec_1948891,Human_Splice_Rec_1948897,Human_Splice_Rec_1948903 111471 RMVar_ID_111471 Human_SNP_ID_832862546 m1A Human chr19 - 38408880 38408880 38408880 GACCCCCCGCCCCCGACCACCAGTCCCCCTTTACTTCTTCTTCTTCTTCTTGCGACCCCAACACT GACCCCCCGCCCCCGACCACCAGTCCCCCTTTTCTTCTTCTTCTTCTTCTTGCGACCCCAACACT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:38408837..38408988 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 111472 RMVar_ID_111472 Human_SNP_ID_832863323 m1A Human chr19 - 58548912 58548912 58548912 TCCACCTCACCCCCAGGGGAGGTGCCATACTTACCGTTTCACACCTGACACATGGGGCTCTGCAC TCCACCTCACCCCCAGGGGAGGTGCCATACTTGCCGTTTCACACCTGACACATGGGGCTCTGCAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:58548799..58549167;chr19:58548797..58549161 26863196 MeRIP-seq:(Medium) rs111630223 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 111473 RMVar_ID_111473 Human_SNP_ID_832863849 m1A Human chr19 - 18924959 18924959 18924959 TCCACTGCTCACCTGCACGGGCCGTCCGGCCGACTCGGTGGATGTAGATCTTGGGGAGCCCGGGG TCCACTGCTCACCTGCACGGGCCGTCCGGCCGGCTCGGTGGATGTAGATCTTGGGGAGCCCGGGG T C AC002985.1 Ensembl:ENSG00000268193 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18924909..18925009 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111474 RMVar_ID_111474 Human_SNP_ID_832865312 m1A Human chr19 - 6416832 6416832 6416832 CCAGGGGGTCCAGGCATGCCCCCGGGGGGCCGAGGCCGAGGAAGAGGCCAAGGCAATTGGGGTCC CCAGGGGGTCCAGGCATGCCCCCGGGGGGCCGTGGCCGAGGAAGAGGCCAAGGCAATTGGGGTCC T A KHSRP Ensembl:ENSG00000088247 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:6416710..6417100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_5372990,Human_RBP_ID_6793095,Human_RBP_ID_8838365,Human_RBP_ID_17933561,Human_RBP_ID_19088914,Human_RBP_ID_22446362,Human_RBP_ID_24559683 Human_Splice_Rec_1944564,Human_Splice_Rec_1944565,Human_Splice_Rec_1944604,Human_Splice_Rec_1944605,Human_Splice_Rec_1944619 111475 RMVar_ID_111475 Human_SNP_ID_832866449 m1A Human chr19 - 35270482 35270482 35270482 CGTGCCTCCCCGCTGACAGCCTCGGCCGCCGGACTGCCACCATTGCTGAAGGGATTTTGGATCAC CGTGCCTCCCCGCTGACAGCCTCGGCCGCCGGGCTGCCACCATTGCTGAAGGGATTTTGGATCAC T C lnc-FAM187B-3 RNACentral:URS00009BF8ED lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:35270476..35270500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111476 RMVar_ID_111476 Human_SNP_ID_832867484 m1A Human chr19 + 7933556 7933556 7933556 GCTGGTACCACTTGGAGTCCTTGTGCAGCACGACCCCCAGGGCCTCCCTGGGGAAGAGGGTGGGC GCTGGTACCACTTGGAGTCCTTGTGCAGCACGCCCCCCAGGGCCTCCCTGGGGAAGAGGGTGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:7933505..7933600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111477 RMVar_ID_111477 Human_SNP_ID_832868609 m1A Human chr19 - 48396194 48396194 48396194 CCTCAGGGATCACAGAGTCCAGCCTCTGGACAACCCCCCGCTCCCCCCGCCTCCATCTCTACCTC CCTCAGGGATCACAGAGTCCAGCCTCTGGACACCCCCCCGCTCCCCCCGCCTCCATCTCTACCTC T G lnc-KDELR1-2 RNACentral:URS0000D5D5E9 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:48396108..48396284 26863196 MeRIP-seq:(Medium) rs886805960 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111478 RMVar_ID_111478 Human_SNP_ID_832868788 m1A Human chr19 - 35871704 35871704 35871704 GTCCCAGATGGGTCGGGGGTCCCTGGAGGGGGACAGCACACATACTCCACACCACGGAACCGATC GTCCCAGATGGGTCGGGGGTCCCTGGAGGGGGGCAGCACACATACTCCACACCACGGAACCGATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:35871655..35871776 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111479 RMVar_ID_111479 Human_SNP_ID_832870892 m1A Human chr19 + 16129598 16129598 16129598 CTCGCCAGAGATATCAAAGCAAAAATGGACAAAAAATTGGTGAGTGTGTGTCCTTCCGAGATCCC CTCGCCAGAGATATCAAAGCAAAAATGGACAACAAATTGGTGAGTGTGTGTCCTTCCGAGATCCC A C RAB8A Ensembl:ENSG00000167461 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:16128018..16129625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_Splice_Rec_1973124,Human_Splice_Rec_1973125,Human_Splice_Rec_1973152,Human_Splice_Rec_1973153,Human_Splice_Rec_1973162,Human_Splice_Rec_1973163 RMVar_hsa_circ_72330,RMVar_hsa_circ_103403,RMVar_hsa_circ_193169,RMVar_hsa_circ_108728,RMVar_hsa_circ_193172 111480 RMVar_ID_111480 Human_SNP_ID_832871376 m1A Human chr19 - 4663295 4663295 4663295 GTAGATTGGAGGCTGTGTAGAATGAGGATGGGATGGGTGGAGAGGGCACAGATTGGAGGCTGTAG GTAGATTGGAGGCTGTGTAGAATGAGGATGGGGTGGGTGGAGAGGGCACAGATTGGAGGCTGTAG T C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4663294..4663407 26863196 MeRIP-seq:(Medium) rs1196305420 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,skin mycosis_fungoides-Sezary_syndrome 2 skin,haematopoietic and lymphoid tissue RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 111481 RMVar_ID_111481 Human_SNP_ID_832871928 m1A Human chr19 + 868351 868340 868351 CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGAGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC CGGGCTCAGGGGCAGCTGAGGG___________GTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC GGTAGCTGAGGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868210..868452 26863196 MeRIP-seq:(Medium) rs3217342 Functional Loss DEL ICGC 23..33 33 CHOL 1 - 111482 RMVar_ID_111482 Human_SNP_ID_832875359 m1A Human chr19 + 3618976 3618976 3618976 CCCGCCAGAAGTCGGCGTTCTTGCCCTGCTCCAGCTCCATGTAGACCTGGGGGCAGGGGGCAGGG CCCGCCAGAAGTCGGCGTTCTTGCCCTGCTCCTGCTCCATGTAGACCTGGGGGCAGGGGGCAGGG A T CACTIN-AS1 RNACentral:URS00008C2E2F lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3618925..3620830 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111483 RMVar_ID_111483 Human_SNP_ID_832877325 m1A Human chr19 - 10554199 10554199 10554199 GCCCACAGAGGCAGCTGCCAGCCCTTGATGGCAGCTTGATGGGGCCGGAGAGTCCCCCAGCACAG GCCCACAGAGGCAGCTGCCAGCCCTTGATGGCGGCTTGATGGGGCCGGAGAGTCCCCCAGCACAG T C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10554149..10554219 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_17914265,Human_RBP_ID_23781006 Human_Splice_Rec_1955074,Human_Splice_Rec_1955110,Human_Splice_Rec_1955146,Human_Splice_Rec_1955162,Human_Splice_Rec_1955198,Human_Splice_Rec_1955232 111484 RMVar_ID_111484 Human_SNP_ID_832881072 m1A Human chr19 - 49490250 49490250 49490250 AATTGCCAGAAATGTTGATGCCTTCACAGCGTACGACCACCACCTTCCGGCCTAGAGGGAGGGAA AATTGCCAGAAATGTTGATGCCTTCACAGCGTTCGACCACCACCTTCCGGCCTAGAGGGAGGGAA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49490226..49490300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111485 RMVar_ID_111485 Human_SNP_ID_832891072 m1A Human chr19 - 43526628 43526628 43526628 GATGTTCGAGCCTGTGAGCTGCACCTTCACGTACCTGCTGGGTGACAGAGAGTCCCGGGAGGCCG GATGTTCGAGCCTGTGAGCTGCACCTTCACGTTCCTGCTGGGTGACAGAGAGTCCCGGGAGGCCG T A ETHE1 Ensembl:ENSG00000105755 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:43526577..43526953 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4558518 Human_Splice_Rec_2015446,Human_Splice_Rec_2015458,Human_Splice_Rec_2015468,Human_Splice_Rec_2015478,Human_Splice_Rec_2015486,Human_Splice_Rec_2015492 Human_miRNA_ID_2223976,Human_miRNA_ID_2487046,Human_miRNA_ID_3075412 RMVar_hsa_circ_8764,RMVar_hsa_circ_112439,RMVar_hsa_circ_122257,RMVar_hsa_circ_195146,RMVar_hsa_circ_195145,RMVar_hsa_circ_273510,RMVar_hsa_circ_90710,RMVar_hsa_circ_195152,RMVar_hsa_circ_195153 111486 RMVar_ID_111486 Human_SNP_ID_832892604 m1A Human chr19 + 45770987 45770987 45770987 GGGCAGCCGGACGTACCCTGGCAGGGAGCAGCAGGTGGCGGCGGTGCATGGGGCCTGGCCCCACC GGGCAGCCGGACGTACCCTGGCAGGGAGCAGCGGGTGGCGGCGGTGCATGGGGCCTGGCCCCACC A G DM1-AS Ensembl:ENSG00000267395 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45770955..45771164 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_263986,Human_RBP_ID_5191649,Human_RBP_ID_18490825 Human_Splice_Rec_2020627,Human_Splice_Rec_2020631,Human_Splice_Rec_2020635 111487 RMVar_ID_111487 Human_SNP_ID_832893480 m1A Human chr19 - 45346641 45346641 45346641 GCCGCCGCTGCGTCTCCTCCAGTTCCTCCCGCAGCCACACGTTCTCCTGGGCCAGCCGCCGGGCC GCCGCCGCTGCGTCTCCTCCAGTTCCTCCCGCTGCCACACGTTCTCCTGGGCCAGCCGCCGGGCC T A lnc-ERCC2-1 RNACentral:URS00009C2807 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45346592..45346746 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver 111488 RMVar_ID_111488 Human_SNP_ID_832896955 m1A Human chr19 - 5047627 5047627 5047627 GCTCCCCAAAGTGCAGGTAGTTGATGCTGTACAGGTCCATGTCCTCGGTGTGCCAGGCGAAGGTG GCTCCCCAAAGTGCAGGTAGTTGATGCTGTACTGGTCCATGTCCTCGGTGTGCCAGGCGAAGGTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:5047570..5047742 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 6 uterus 111489 RMVar_ID_111489 Human_SNP_ID_832897196 m1A Human chr19 - 24001321 24001317 24001322 GTCCCAGGTGCAGATCTTGGTGGTAGTAGCAAATATTCAAATGAGAACTTTGAAGGCCGAAGTGG GTCCCAGGTGCAGATCTTGGTGGTAGTAGCA_____TCAAATGAGAACTTTGAAGGCCGAAGTGG AATATT A RF02543-023 RNACentral:URS00009843EB rRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr19:24001233..24001406;chr19:24001219..24001412;chr19:24001263..24001382 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..36 33 NKTL 1 - Human_RBP_ID_270072,Human_RBP_ID_279375,Human_RBP_ID_518086,Human_RBP_ID_1014135,Human_RBP_ID_1094780,Human_RBP_ID_1132841,Human_RBP_ID_1188168,Human_RBP_ID_1239750,Human_RBP_ID_1292815,Human_RBP_ID_1372380,Human_RBP_ID_1557954,Human_RBP_ID_1882124,Human_RBP_ID_2561366,Human_RBP_ID_3566047,Human_RBP_ID_4564900,Human_RBP_ID_5190587,Human_RBP_ID_5261363,Human_RBP_ID_5275391,Human_RBP_ID_5421334,Human_RBP_ID_5442854,Human_RBP_ID_5468507,Human_RBP_ID_5499232,Human_RBP_ID_5585542,Human_RBP_ID_6733694,Human_RBP_ID_8096251,Human_RBP_ID_8255913,Human_RBP_ID_8481574,Human_RBP_ID_8831124,Human_RBP_ID_9085570,Human_RBP_ID_9258564,Human_RBP_ID_9291618,Human_RBP_ID_9910911,Human_RBP_ID_13415437,Human_RBP_ID_17009952,Human_RBP_ID_17068497,Human_RBP_ID_17190606,Human_RBP_ID_17267464,Human_RBP_ID_17382686,Human_RBP_ID_17498497,Human_RBP_ID_17695026,Human_RBP_ID_17918675,Human_RBP_ID_18179856,Human_RBP_ID_18200508,Human_RBP_ID_18208356,Human_RBP_ID_18302601,Human_RBP_ID_18440902,Human_RBP_ID_18514808,Human_RBP_ID_18533155,Human_RBP_ID_18726173,Human_RBP_ID_19031282,Human_RBP_ID_20368619,Human_RBP_ID_21891623,Human_RBP_ID_21929794,Human_RBP_ID_22005118,Human_RBP_ID_22391142,Human_RBP_ID_22422473,Human_RBP_ID_22502094,Human_RBP_ID_22810214,Human_RBP_ID_22968254,Human_RBP_ID_23130899,Human_RBP_ID_23277842,Human_RBP_ID_23309457,Human_RBP_ID_23789419,Human_RBP_ID_24418599,Human_RBP_ID_24484013,Human_RBP_ID_24532605,Human_RBP_ID_24538893,Human_RBP_ID_24540133,Human_RBP_ID_25392853,Human_RBP_ID_26474702,Human_RBP_ID_26651774,Human_RBP_ID_26749436,Human_RBP_ID_26987262,Human_RBP_ID_27157449,Human_RBP_ID_27271556,Human_RBP_ID_27466231,Human_RBP_ID_27562296,Human_RBP_ID_27675952 111490 RMVar_ID_111490 Human_SNP_ID_832898034 m1A Human chr19 - 11176805 11176805 11176805 CCCCGCTCGTTCCTCCCCAGGTATGAGTCGTCATCCGAGGACTCCAGCACAGCAGAGAACATCTC CCCCGCTCGTTCCTCCCCAGGTATGAGTCGTCCTCCGAGGACTCCAGCACAGCAGAGAACATCTC T G KANK2 Ensembl:ENSG00000197256 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11176755..11178564 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_Splice_Rec_1959468,Human_Splice_Rec_1959504,Human_Splice_Rec_1959524 RMVar_hsa_circ_77650,RMVar_hsa_circ_192534,RMVar_hsa_circ_353819,RMVar_hsa_circ_334841,RMVar_hsa_circ_47942,RMVar_hsa_circ_192536,RMVar_hsa_circ_192537,RMVar_hsa_circ_325416,RMVar_hsa_circ_192542,RMVar_hsa_circ_192538,RMVar_hsa_circ_84640,RMVar_hsa_circ_286033,RMVar_hsa_circ_47952,RMVar_hsa_circ_192541 111491 RMVar_ID_111491 Human_SNP_ID_832902933 m1A Human chr19 - 4817354 4817354 4817354 AGACGCCACTCCAACTTTCTGTAGAAGATACCACCTCTCCAAATACCAAGCCGTGCCCACCTACT AGACGCCACTCCAACTTTCTGTAGAAGATACCGCCTCTCCAAATACCAAGCCGTGCCCACCTACT T C TICAM1 Ensembl:ENSG00000127666 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4817304..4817387 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_27276576,Human_RBP_ID_27469894 111492 RMVar_ID_111492 Human_SNP_ID_832911763 m1A Human chr19 - 41292374 41292374 41292374 TGCTCTCTGTCCGAAGTTGAACTCCACTGCGCAATTCTTCACCAGGACATGAGGATAGAGGGCCT TGCTCTCTGTCCGAAGTTGAACTCCACTGCGCGATTCTTCACCAGGACATGAGGATAGAGGGCCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:41292324..41292425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 11 large intestine RMVar_hsa_circ_195005 111493 RMVar_ID_111493 Human_SNP_ID_832911926 m1A Human chr19 + 12801263 12801260 12801264 GCTTTCCGATGCGCGCGTTACCGGAGGCCATGACTGAAAGCTGAGACCCCCGCCCGGTCAGTGCG GCTTTCCGATGCGCGCGTTACCGGAGGCCA____TGAAAGCTGAGACCCCCGCCCGGTCAGTGCG ATGAC A AC018761.2 Ensembl:ENSG00000267062 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:12801001..12801875 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 PBCA 1 - 111494 RMVar_ID_111494 Human_SNP_ID_832913151 m1A Human chr19 + 45584749 45584749 45584749 GATGCCCAAGTATAGCAGCTTCGCCATAGGGAACGCGCCCACCACCATCTTGGCGGTCTCACAGG GATGCCCAAGTATAGCAGCTTCGCCATAGGGACCGCGCCCACCACCATCTTGGCGGTCTCACAGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45584579..45584804 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 111495 RMVar_ID_111495 Human_SNP_ID_832915189 m1A Human chr19 - 55385955 55385955 55385955 CGCGAGGAAGACGAACGCTCACCTCCCTTCGCAGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG CGCGAGGAAGACGAACGCTCACCTCCCTTCGCTGCGGCGACCTGAGACGGAAAGAGGAAGGCGAG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:55385926..55385975 26863196 MeRIP-seq:(Medium) rs562997171 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111496 RMVar_ID_111496 Human_SNP_ID_832916136 m1A Human chr19 + 2802442 2802442 2802442 CCCACCTCCCGACACCCCCACCTCCCAACACCAACACCTCCCGACACCCCCACCTCCCGACACCA CCCACCTCCCGACACCCCCACCTCCCAACACCCACACCTCCCGACACCCCCACCTCCCGACACCA A C THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:2802435..2802614 26863196 MeRIP-seq:(Medium) rs1347747747 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_111400,RMVar_hsa_circ_191285,RMVar_hsa_circ_191286 111497 RMVar_ID_111497 Human_SNP_ID_832916686 m1A Human chr19 + 55689356 55689354 55689356 GCCCAGCTCCAGCTGGCCCTTAGTTTGAGCCGAGAAGAGCATGATAAGGTCAGAGCAGCCTCCCT GCCCAGCTCCAGCTGGCCCTTAGTTTGAGCC__GAAGAGCATGATAAGGTCAGAGCAGCCTCCCT CGA C EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55689276..55689375 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 CHOL 1 - Human_RBP_ID_5117620 Human_Splice_Rec_2048020,Human_Splice_Rec_2048021,Human_Splice_Rec_2048076,Human_Splice_Rec_2048077 RMVar_hsa_circ_9292,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196364,RMVar_hsa_circ_331802 111498 RMVar_ID_111498 Human_SNP_ID_832917766 m1A Human chr19 + 10310935 10310935 10310935 ATGGCAGGTGGAGCAGGCCAGGGAGGCTTCACAGGCCCCTAGGGGTGGGAAGTGAAGGGGGCGCA ATGGCAGGTGGAGCAGGCCAGGGAGGCTTCACTGGCCCCTAGGGGTGGGAAGTGAAGGGGGCGCA A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10310890..10315379 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111499 RMVar_ID_111499 Human_SNP_ID_832919211 m1A Human chr19 + 47067263 47067263 47067263 GCAGCCGGGGGTCCAGGGTGGGCATGGATTGCAGGGCCGCGGGCACGGGGGGCACTGCGTCCTGC GCAGCCGGGGGTCCAGGGTGGGCATGGATTGCTGGGCCGCGGGCACGGGGGGCACTGCGTCCTGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:47067124..47067300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 111500 RMVar_ID_111500 Human_SNP_ID_832924173 m1A Human chr19 + 18759586 18759564 18759587 GGGTCCAGGCCCAAGTCCTGTGAGGTCCCCGGAATCAAGTAAGTCTCCACAGGGCCCACCCCGCA GGGTCCAGGCC_______________________TCAAGTAAGTCTCCACAGGGCCCACCCCGCA CCAAGTCCTGTGAGGTCCCCGGAA C CRTC1 Ensembl:ENSG00000105662 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18753499..18760080 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 12..34 33 KIRP 1 - Human_Splice_Rec_1980964,Human_Splice_Rec_1980965,Human_Splice_Rec_1980988,Human_Splice_Rec_1980989,Human_Splice_Rec_1981012,Human_Splice_Rec_1981013,Human_Splice_Rec_1981034,Human_Splice_Rec_1981035 RMVar_hsa_circ_5218 111501 RMVar_ID_111501 Human_SNP_ID_832926780 m1A Human chr19 - 1612365 1612365 1612365 CCTGAGGGACCGGGAGAGGCGCATGGCCAATAACGCGCGGGAGCGGGTGCGCGTGCGGGATATTA CCTGAGGGACCGGGAGAGGCGCATGGCCAATACCGCGCGGGAGCGGGTGCGCGTGCGGGATATTA T G TCF3 Ensembl:ENSG00000071564 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:1612226..1615288;chr19:1612201..1612474 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4507533,Human_RBP_ID_17916416 Human_Splice_Rec_1933528,Human_Splice_Rec_1933562,Human_Splice_Rec_1933568,Human_Splice_Rec_1933642,Human_Splice_Rec_1933694,Human_Splice_Rec_1933706,Human_Splice_Rec_1933714,Human_Splice_Rec_1933722,Human_Splice_Rec_1933732,Human_Splice_Rec_1933772 RMVar_hsa_circ_267745,RMVar_hsa_circ_34083 111502 RMVar_ID_111502 Human_SNP_ID_832930905 m1A Human chr19 - 18598845 18598845 18598845 TCAGCTGCTGGTCCAAGAACATGAAGGACTTGACCTGCCGCTGGACGCCAGGGGCCCACGGGGAG TCAGCTGCTGGTCCAAGAACATGAAGGACTTGCCCTGCCGCTGGACGCCAGGGGCCCACGGGGAG T G CRLF1 Ensembl:ENSG00000006016 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18598745..18598938 26863196 MeRIP-seq:(Medium) rs758469818 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_22447592,Human_RBP_ID_22764006 Human_Splice_Rec_1980808,Human_Splice_Rec_1980809 RMVar_hsa_circ_126318,RMVar_hsa_circ_193509,RMVar_hsa_circ_89748,RMVar_hsa_circ_193511,RMVar_hsa_circ_118825,RMVar_hsa_circ_362274,RMVar_hsa_circ_193512 111503 RMVar_ID_111503 Human_SNP_ID_832931777 m1A Human chr19 + 13929420 13929420 13929420 GCCCCTGCATAGCCTCAGTGTGCTGGCGTTTGACCAAGAGCGTCTGGAGCGGAAGGTGGGTATCC GCCCCTGCATAGCCTCAGTGTGCTGGCGTTTGGCCAAGAGCGTCTGGAGCGGAAGGTGGGTATCC A G CC2D1A Ensembl:ENSG00000132024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:13927814..13930108 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_240344,Human_RBP_ID_5585399 Human_Splice_Rec_1967396,Human_Splice_Rec_1967397,Human_Splice_Rec_1967470,Human_Splice_Rec_1967471,Human_Splice_Rec_1967516,Human_Splice_Rec_1967517,Human_Splice_Rec_1967554,Human_Splice_Rec_1967555,Human_Splice_Rec_1967590,Human_Splice_Rec_1967591 Human_miRNA_ID_1604447,Human_miRNA_ID_1678697 RMVar_hsa_circ_101859,RMVar_hsa_circ_192946 111504 RMVar_ID_111504 Human_SNP_ID_832933865 m1A Human chr19 + 1043424 1043424 1043424 CTGGAGACGCCTGAAGCCTCTGATCCTCGGGAAGCTACTCTTTGCACCAGATACACCTTTTACCC CTGGAGACGCCTGAAGCCTCTGATCCTCGGGATGCTACTCTTTGCACCAGATACACCTTTTACCC A T ABCA7 Ensembl:ENSG00000064687 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1043374..1043509 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_27815729 Human_Splice_Rec_1930044,Human_Splice_Rec_1930045,Human_Splice_Rec_1930142,Human_Splice_Rec_1930143 111505 RMVar_ID_111505 Human_SNP_ID_832941653 m1A Human chr19 - 1605409 1605409 1605409 CAGGGTCATCCTGAGGGTGCGACTCCGCCGCGATGGTGACCCGGTTCCTGGGCCCACGCTACCGG CAGGGTCATCCTGAGGGTGCGACTCCGCCGCGGTGGTGACCCGGTTCCTGGGCCCACGCTACCGG T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding start codon,start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:1602409..1605475;chr19:1605297..1605475 26863196 MeRIP-seq:(Medium) rs1487630794 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_240109,Human_RBP_ID_514972,Human_RBP_ID_771385,Human_RBP_ID_826240,Human_RBP_ID_1555993,Human_RBP_ID_4557014,Human_RBP_ID_5144847,Human_RBP_ID_5319822,Human_RBP_ID_8478845,Human_RBP_ID_9328115,Human_RBP_ID_17655287,Human_RBP_ID_18421519,Human_RBP_ID_22446293,Human_RBP_ID_22501826,Human_RBP_ID_23130784,Human_RBP_ID_23784745,Human_RBP_ID_26984481 Human_Splice_Rec_1933465,Human_Splice_Rec_1933477,Human_Splice_Rec_1933485,Human_Splice_Rec_1933489,Human_Splice_Rec_1933495 Human_miRNA_ID_3089116 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 111506 RMVar_ID_111506 Human_SNP_ID_832945820 m1A Human chr19 + 17338105 17338105 17338105 GCTCTGGCCAAGGCCGCTGCGGCATCGCAGTGATCCGGACCAGCGGCCCCGCCAGCGGCCACGCC GCTCTGGCCAAGGCCGCTGCGGCATCGCAGTGGTCCGGACCAGCGGCCCCGCCAGCGGCCACGCC A G GTPBP3 Ensembl:ENSG00000130299 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17338059..17338174 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4509153,Human_RBP_ID_13392153,Human_RBP_ID_18724295,Human_RBP_ID_22967658,Human_RBP_ID_23786145,Human_RBP_ID_26815482 Human_Splice_Rec_1976562,Human_Splice_Rec_1976578,Human_Splice_Rec_1976586,Human_Splice_Rec_1976606,Human_Splice_Rec_1976612,Human_Splice_Rec_1976618,Human_Splice_Rec_1976624,Human_Splice_Rec_1976626,Human_Splice_Rec_1976640,Human_Splice_Rec_1976652,Human_Splice_Rec_1976682,Human_Splice_Rec_1976712 111507 RMVar_ID_111507 Human_SNP_ID_832950088 m1A Human chr19 + 10254637 10254637 10254637 CAGGTTGCTATGTGGCAGAAGAACTTCAAGAGAATTGTGAGTGCCTAAATGGAGCAAGGTGGTGG CAGGTTGCTATGTGGCAGAAGAACTTCAAGAGGATTGTGAGTGCCTAAATGGAGCAAGGTGGTGG A G MRPL4 Ensembl:ENSG00000105364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:10254536..10254691;chr19:10254576..10254650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 6 liver Human_RBP_ID_1553532,Human_RBP_ID_1879441,Human_RBP_ID_4560084,Human_RBP_ID_5371262,Human_RBP_ID_13357502,Human_RBP_ID_18996482 Human_Splice_Rec_1953878,Human_Splice_Rec_1953879,Human_Splice_Rec_1953896,Human_Splice_Rec_1953897,Human_Splice_Rec_1953910,Human_Splice_Rec_1953911,Human_Splice_Rec_1953926,Human_Splice_Rec_1953927,Human_Splice_Rec_1953936,Human_Splice_Rec_1953937,Human_Splice_Rec_1953950,Human_Splice_Rec_1953951,Human_Splice_Rec_1953966,Human_Splice_Rec_1953967,Human_Splice_Rec_1953980,Human_Splice_Rec_1953984,Human_Splice_Rec_1953985,Human_Splice_Rec_1953995 RMVar_hsa_circ_116491,RMVar_hsa_circ_98538,RMVar_hsa_circ_192329,RMVar_hsa_circ_192330 111508 RMVar_ID_111508 Human_SNP_ID_832951520 m1A Human chr19 - 6459696 6459696 6459696 CGGGAGCTGACCCTGCGGGGTCCCGGGGGGGGAGGGGGAGCCGCGAAGCCCCCACTGAGGCCGCC CGGGAGCTGACCCTGCGGGGTCCCGGGGGGGGGGGGGGAGCCGCGAAGCCCCCACTGAGGCCGCC T C SLC25A23 Ensembl:ENSG00000125648 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:6459526..6459775 26863410 MeRIP-seq:(Medium) rs537137506 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4557158,Human_RBP_ID_5239221 RMVar_hsa_circ_79615,RMVar_hsa_circ_191830,RMVar_hsa_circ_266857 111509 RMVar_ID_111509 Human_SNP_ID_832954043 m1A Human chr19 + 48501551 48501551 48501551 CGGTCAGGTCAGAGGTCAGCAGGCAGTTGCGCAGGGCCAGGTCGCTGCGGGAAGAACGCGAGGAG CGGTCAGGTCAGAGGTCAGCAGGCAGTTGCGCTGGGCCAGGTCGCTGCGGGAAGAACGCGAGGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48501369..48501847 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111510 RMVar_ID_111510 Human_SNP_ID_832958032 m1A Human chr19 - 19647491 19647491 19647491 CCTGAGCCAGGTGCTGCGAGACCTCGAGGACGAGAGTACGCCCATTGTGAAACTGGGGGATGCCA CCTGAGCCAGGTGCTGCGAGACCTCGAGGACGGGAGTACGCCCATTGTGAAACTGGGGGATGCCA T C ATP13A1 Ensembl:ENSG00000105726 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19647440..19649647 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 6 ovary Human_RBP_ID_907611,Human_RBP_ID_3954799,Human_RBP_ID_5371575,Human_RBP_ID_18165721,Human_RBP_ID_22742474 Human_Splice_Rec_1983874,Human_Splice_Rec_1983875,Human_Splice_Rec_1983924,Human_Splice_Rec_1983925,Human_Splice_Rec_1983942,Human_Splice_Rec_1983943,Human_Splice_Rec_1983968,Human_Splice_Rec_1983969,Human_Splice_Rec_1984001 Human_miRNA_ID_2924430 RMVar_hsa_circ_117158,RMVar_hsa_circ_320198,RMVar_hsa_circ_119863,RMVar_hsa_circ_115848,RMVar_hsa_circ_193668,RMVar_hsa_circ_193670,RMVar_hsa_circ_193672,RMVar_hsa_circ_76597,RMVar_hsa_circ_193671,RMVar_hsa_circ_193669,RMVar_hsa_circ_58241,RMVar_hsa_circ_193675,RMVar_hsa_circ_101579,RMVar_hsa_circ_265481,RMVar_hsa_circ_80617,RMVar_hsa_circ_5251,RMVar_hsa_circ_273296,RMVar_hsa_circ_193676,RMVar_hsa_circ_193677 111511 RMVar_ID_111511 Human_SNP_ID_832971863 m1A Human chr19 - 16528150 16528150 16528150 AGCTGCCGGCCCCCGGGGCCCCGGGCCACACGACCAGATCCCACCAAACAAGCCCCCTTGGTTTG AGCTGCCGGCCCCCGGGGCCCCGGGCCACACGGCCAGATCCCACCAAACAAGCCCCCTTGGTTTG T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:16528046..16528303;chr19:16528101..16528275;chr19:16528041..16528275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_54929,Human_RBP_ID_240945,Human_RBP_ID_17387300 Human_Splice_Rec_1973969,Human_Splice_Rec_1974001 111512 RMVar_ID_111512 Human_SNP_ID_832972117 m1A Human chr19 - 8511811 8511811 8511811 GCCGCCCGCGCCGGAGCGCCCCCCGGAGGTTGACCCCGCATCAGCGCCGGGCCTGCCGTTCCCGC GCCGCCCGCGCCGGAGCGCCCCCCGGAGGTTGGCCCCGCATCAGCGCCGGGCCTGCCGTTCCCGC T C ZNF414 Ensembl:ENSG00000133250 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr19:8511759..8511859 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_4555812 111513 RMVar_ID_111513 Human_SNP_ID_832972179 m1A Human chr19 - 43798928 43798928 43798928 GAAGGGCTGCTGGACCGGGCCTCCTGCGGGCCAGACGCAATCGAACGCGGACGCGCTGCCGCCAG GAAGGGCTGCTGGACCGGGCCTCCTGCGGGCCGGACGCAATCGAACGCGGACGCGCTGCCGCCAG T C LYPD5 Ensembl:ENSG00000159871 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43798888..43799010 32194978 MeRIP-seq:(Medium) rs536675872 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_2016108,Human_Splice_Rec_2016118,Human_Splice_Rec_2016126,Human_Splice_Rec_2016132,Human_Splice_Rec_2016146,Human_Splice_Rec_2016152 111514 RMVar_ID_111514 Human_SNP_ID_832974396 m1A Human chr19 - 17327257 17327257 17327257 CTGGGTGGCCGAGGAAATGGCCAAGCTGGAGTACCAGCGCCGCGAGGCCTTTAAGGTAGGGGGGC CTGGGTGGCCGAGGAAATGGCCAAGCTGGAGTGCCAGCGCCGCGAGGCCTTTAAGGTAGGGGGGC T C ANO8 Ensembl:ENSG00000074855 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17324900..17328336 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_1976500,Human_Splice_Rec_1976501,Human_Splice_Rec_1976532,Human_Splice_Rec_1976533 RMVar_hsa_circ_8490,RMVar_hsa_circ_102865,RMVar_hsa_circ_349484,RMVar_hsa_circ_193306,RMVar_hsa_circ_16443 111515 RMVar_ID_111515 Human_SNP_ID_832974508 m1A Human chr19 - 45854499 45854499 45854499 ATCCTCTTCTTTCCTGGGGACAAGCTGACAGCAGCCATGGCGAGCGGCAGTGGAGACAGCGTCAC ATCCTCTTCTTTCCTGGGGACAAGCTGACAGCTGCCATGGCGAGCGGCAGTGGAGACAGCGTCAC T A SYMPK Ensembl:ENSG00000125755 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:45854441..45854547 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_523867,Human_RBP_ID_911615,Human_RBP_ID_1568479,Human_RBP_ID_3957201,Human_RBP_ID_5376994,Human_RBP_ID_8840145,Human_RBP_ID_9294467,Human_RBP_ID_18998224,Human_RBP_ID_19090463,Human_RBP_ID_22546877,Human_RBP_ID_22665632,Human_RBP_ID_22978124,Human_RBP_ID_23114779,Human_RBP_ID_23257557 Human_Splice_Rec_2021050,Human_Splice_Rec_2021102,Human_Splice_Rec_2021226,Human_Splice_Rec_2021308,Human_Splice_Rec_2021342,Human_Splice_Rec_2021352,Human_Splice_Rec_2021364,Human_Splice_Rec_2021374,Human_Splice_Rec_2021380 RMVar_hsa_circ_346786,RMVar_hsa_circ_127715,RMVar_hsa_circ_79946,RMVar_hsa_circ_195422,RMVar_hsa_circ_105011,RMVar_hsa_circ_195423,RMVar_hsa_circ_195424,RMVar_hsa_circ_76710,RMVar_hsa_circ_195425,RMVar_hsa_circ_93866,RMVar_hsa_circ_331450,RMVar_hsa_circ_195426,RMVar_hsa_circ_195433,RMVar_hsa_circ_355438,RMVar_hsa_circ_12162,RMVar_hsa_circ_97712,RMVar_hsa_circ_195438,RMVar_hsa_circ_308553,RMVar_hsa_circ_344501,RMVar_hsa_circ_195440,RMVar_hsa_circ_291775,RMVar_hsa_circ_195442,RMVar_hsa_circ_92180,RMVar_hsa_circ_270494,RMVar_hsa_circ_314251,RMVar_hsa_circ_195445,RMVar_hsa_circ_195446,RMVar_hsa_circ_195447 111516 RMVar_ID_111516 Human_SNP_ID_832978000 m1A Human chr19 - 19633888 19633888 19633888 ACCGCCACCCCCGCACCTTGACCCAGACTCCCAGCCCCCAGTCCTAGCCTCAGACCCCGGCCCAG ACCGCCACCCCCGCACCTTGACCCAGACTCCCGGCCCCCAGTCCTAGCCTCAGACCCCGGCCCAG T C GMIP Ensembl:ENSG00000089639 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:19633839..19633961 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_17082402 Human_Splice_Rec_1983721,Human_Splice_Rec_1983759 RMVar_hsa_circ_103925,RMVar_hsa_circ_115029,RMVar_hsa_circ_193660,RMVar_hsa_circ_193661 111517 RMVar_ID_111517 Human_SNP_ID_832984489 m1A Human chr19 - 54115490 54115490 54115490 CGTTGGCAACTCAGAGGACTGGTTGCGGCGTTAGACAAGAAAGCAAGGCCTTTAAGCAGGGATTC CGTTGGCAACTCAGAGGACTGGTTGCGGCGTTGGACAAGAAAGCAAGGCCTTTAAGCAGGGATTC T C TFPT Ensembl:ENSG00000105619 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:54115440..54115582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4572763 111518 RMVar_ID_111518 Human_SNP_ID_832984761 m1A Human chr19 + 1853206 1853206 1853206 CACCCCACCCAAGTTCAGCTCAGAGACCCCCCACACACACTCACACCCCCTGAGGATGCCGGACC CACCCCACCCAAGTTCAGCTCAGAGACCCCCCCCACACACTCACACCCCCTGAGGATGCCGGACC A C AC012615.3 Ensembl:ENSG00000267125 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1853155..1853234 26863196 MeRIP-seq:(Medium) rs550342319 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 111519 RMVar_ID_111519 Human_SNP_ID_832985824 m1A Human chr19 - 45402694 45402694 45402694 AGCTAGAGGGGAGCACATGGGAGAGGACTCGGAGGCAGAGGTCAGGGGCAGAGGCCTGGGAACAG AGCTAGAGGGGAGCACATGGGAGAGGACTCGGTGGCAGAGGTCAGGGGCAGAGGCCTGGGAACAG T A PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45402691..45402799 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 111520 RMVar_ID_111520 Human_SNP_ID_832987470 m1A Human chr19 + 49836350 49836350 49836350 GGGGCAGCCCCAGTTGGGGCCCCCACTCCTGCATCCACCACCTGCCCAGTCCTGGCCCGCACAAC GGGGCAGCCCCAGTTGGGGCCCCCACTCCTGCCTCCACCACCTGCCCAGTCCTGGCCCGCACAAC A C MED25 Ensembl:ENSG00000104973 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49835016..49836471 32194978 MeRIP-seq:(Medium) rs564170396 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 8 lung Human_RBP_ID_525610 Human_Splice_Rec_2032643,Human_Splice_Rec_2032661,Human_Splice_Rec_2032669,Human_Splice_Rec_2032679,Human_Splice_Rec_2032719,Human_Splice_Rec_2032753,Human_Splice_Rec_2032789,Human_Splice_Rec_2032821 111521 RMVar_ID_111521 Human_SNP_ID_832988739 m1A Human chr19 + 10829150 10829150 10829150 ACCAGGCACAGCGGCGGGACGACATGCTGCGCATGTACCATGCCCTCAAGGAGGCGCTCAACATC ACCAGGCACAGCGGCGGGACGACATGCTGCGCGTGTACCATGCCCTCAAGGAGGCGCTCAACATC A G DNM2 Ensembl:ENSG00000079805 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10829100..10829304 26863196 MeRIP-seq:(Medium) rs757876109 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_22809037 Human_miRNA_ID_2493940,Human_miRNA_ID_2696240 RMVar_hsa_circ_80209,RMVar_hsa_circ_192444,RMVar_hsa_circ_52653 111522 RMVar_ID_111522 Human_SNP_ID_832991134 m1A Human chr19 + 46697251 46697250 46697252 AATAGTGCCGCTTTCTCTGCAGAGATGTTTGAAGAGTCACGTGAACCGCCAGACTTTCCTGCCCA AATAGTGCCGCTTTCTCTGCAGAGATGTTTGA__AGTCACGTGAACCGCCAGACTTTCCTGCCCA AAG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46697249..46697377 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 PBCA 1 - 111523 RMVar_ID_111523 Human_SNP_ID_832995659 m1A Human chr19 + 48616775 48616775 48616775 CCTGAACCCGCACATCATCAGTTATGGTCCCCACAACCACGGCCGTCTTGTTTTCCCGGCCAGGA CCTGAACCCGCACATCATCAGTTATGGTCCCCCCAACCACGGCCGTCTTGTTTTCCCGGCCAGGA A C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr19:48616674..48616841;chr19:48616672..48616867;chr19:48616614..48616800 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - 111524 RMVar_ID_111524 Human_SNP_ID_833000496 m1A Human chr19 + 7924943 7924943 7924943 GAGGAGGGACAAGGGGGTCCCCACTTCCAGGGACGCACAATAGCAGAGCCACTTACACGCTGGGG GAGGAGGGACAAGGGGGTCCCCACTTCCAGGGGCGCACAATAGCAGAGCCACTTACACGCTGGGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7924582..7925024 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 111525 RMVar_ID_111525 Human_SNP_ID_833002324 m1A Human chr19 - 36141155 36141155 36141155 ATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC ATGGCCGTTCCACCGCCACCGCCGCCTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEPG2 cell line,total RNA rearranged at 50c;HEK293T,Starvation treatment chr19:36140959..36141296;chr19:36140976..36141339 26863196,26863410 MeRIP-seq:(Medium) rs538969591 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 9 head and neck 111526 RMVar_ID_111526 Human_SNP_ID_833005815 m1A Human chr19 - 12721452 12721452 12721452 TCTGGCAGAAGTTAAGGGCAGAGTGTCGGGGGAAGGGGACTCTTCAGGGACTGTGCCTGCATAGA TCTGGCAGAAGTTAAGGGCAGAGTGTCGGGGGGAGGGGACTCTTCAGGGACTGTGCCTGCATAGA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12721443..12722300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_825385,Human_RBP_ID_3580876,Human_RBP_ID_6720934,Human_RBP_ID_13371363,Human_RBP_ID_17190812,Human_RBP_ID_23782766 RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192741,RMVar_hsa_circ_192763,RMVar_hsa_circ_102292,RMVar_hsa_circ_101720,RMVar_hsa_circ_192764,RMVar_hsa_circ_192765,RMVar_hsa_circ_192772,RMVar_hsa_circ_116785,RMVar_hsa_circ_192774,RMVar_hsa_circ_372945 111527 RMVar_ID_111527 Human_SNP_ID_833006886 m1A Human chr19 + 44813340 44813340 44813340 ACGGGCAGCGCCTGGAGGTGCCCGTAGAGATGAACCCAGGTGAGCAGCGCAGGAGCGCGGCGGGA ACGGGCAGCGCCTGGAGGTGCCCGTAGAGATGGACCCAGGTGAGCAGCGCAGGAGCGCGGCGGGA A G BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:44813327..44813424 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_18998039 Human_Splice_Rec_2017708,Human_Splice_Rec_2017709,Human_Splice_Rec_2017734,Human_Splice_Rec_2017735,Human_Splice_Rec_2017764,Human_Splice_Rec_2017765,Human_Splice_Rec_2017775 111528 RMVar_ID_111528 Human_SNP_ID_833017673 m1A Human chr19 - 13913517 13913517 13913517 GACGCGATTCTAGGGGCCGGCTGGGTGGGTGCAGGGCTGTAGGTAGGCGTGGACGCCGGGCCTTT GACGCGATTCTAGGGGCCGGCTGGGTGGGTGCGGGGCTGTAGGTAGGCGTGGACGCCGGGCCTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:13913472..13913649 26863196 MeRIP-seq:(Medium) rs753037271 Functional Loss SNV ICGC 33..33 33 COCA 1 - Clinvar_Rec_424 111529 RMVar_ID_111529 Human_SNP_ID_833024227 m1A Human chr19 - 2213637 2213637 2213637 CCTGCCACCTGCCCTCTGGGGTCCACTACCTCATCCAATTTTTGCTGAAACAGCCTCCTGATCTC CCTGCCACCTGCCCTCTGGGGTCCACTACCTCCTCCAATTTTTGCTGAAACAGCCTCCTGATCTC T G AC004490.1 Ensembl:ENSG00000267122 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2213607..2214156 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 1 breast 111530 RMVar_ID_111530 Human_SNP_ID_833025946 m1A Human chr19 - 10333482 10333482 10333482 TCCCAAGATGGCGGCGGACGTGTCCGTTACTCACCGGCCCCCGCTGAGCCCTAAGTCTGGGGCCG TCCCAAGATGGCGGCGGACGTGTCCGTTACTCGCCGGCCCCCGCTGAGCCCTAAGTCTGGGGCCG T C RAVER1 Ensembl:ENSG00000161847 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:10333301..10333525;chr19:10333276..10333525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_55490,Human_RBP_ID_512101,Human_RBP_ID_4558053,Human_RBP_ID_8839745,Human_RBP_ID_9293364,Human_RBP_ID_22069689,Human_RBP_ID_22446414 111531 RMVar_ID_111531 Human_SNP_ID_833026614 m1A Human chr19 - 48473778 48473778 48473778 CCGACCTTCCGGCCTCAGCAGTTGTTTCAGGTATGGTCACATGATCCAGTCTCACCAATGGGCAT CCGACCTTCCGGCCTCAGCAGTTGTTTCAGGTGTGGTCACATGATCCAGTCTCACCAATGGGCAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48473773..48473874 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111532 RMVar_ID_111532 Human_SNP_ID_833028785 m1A Human chr19 + 1010462 1010462 1010462 TTGTGTCAGAAGCTGCGGAGTCACTCGGGGGGACACTGTCCTGGGGGGCGTGGGGGAGGCCCCCA TTGTGTCAGAAGCTGCGGAGTCACTCGGGGGGGCACTGTCCTGGGGGGCGTGGGGGAGGCCCCCA A G AC004528.2 Ensembl:ENSG00000274177 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:1010451..1010646 26863196 MeRIP-seq:(Medium) rs1190761786 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111533 RMVar_ID_111533 Human_SNP_ID_833028881 m1A Human chr19 - 48806633 48806633 48806633 CCGGCGAGCCCCTGGTGTTTGGGAAGACATTTACCGACCACATGCTGATGGTGGAATGGAATGAC CCGGCGAGCCCCTGGTGTTTGGGAAGACATTTTCCGACCACATGCTGATGGTGGAATGGAATGAC T A BCAT2 Ensembl:ENSG00000105552 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48806583..48807035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_4571572,Human_RBP_ID_18441780,Human_RBP_ID_18737162,Human_RBP_ID_22449570 Human_Splice_Rec_2027508,Human_Splice_Rec_2027530,Human_Splice_Rec_2027548,Human_Splice_Rec_2027570,Human_Splice_Rec_2027610,Human_Splice_Rec_2027626,Human_Splice_Rec_2027638 RMVar_hsa_circ_10100,RMVar_hsa_circ_195722 111534 RMVar_ID_111534 Human_SNP_ID_833031159 m1A Human chr19 + 40192216 40192216 40192216 GGTGTCCGGCGACGAGGGCTGGTGGACCGGGCAGCTCCCCAGCGGCCGCGTGGGCGTCTTCCCCA GGTGTCCGGCGACGAGGGCTGGTGGACCGGGCTGCTCCCCAGCGGCCGCGTGGGCGTCTTCCCCA A T MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:40192096..40192223 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_825691,Human_RBP_ID_5527011 RMVar_hsa_circ_82002,RMVar_hsa_circ_194828 111535 RMVar_ID_111535 Human_SNP_ID_833031204 m1A Human chr19 + 582775 582775 582775 TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCACGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT TCCACAGGTGGCCCGAGGACGCTCCCTGCTCCGCGTCTGCGCCGCCGCCGGAGTCCACTCCCAGT A G BSG Ensembl:ENSG00000172270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8637 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_528158,Human_RBP_ID_772100,Human_RBP_ID_825640,Human_RBP_ID_913671,Human_RBP_ID_4550772,Human_RBP_ID_8495199,Human_RBP_ID_17386490,Human_RBP_ID_17655277,Human_RBP_ID_18740724,Human_RBP_ID_22446254,Human_RBP_ID_22533230,Human_RBP_ID_22763533,Human_RBP_ID_26475210 Human_Splice_Rec_1928476,Human_Splice_Rec_1928488,Human_Splice_Rec_1928512,Human_Splice_Rec_1928528,Human_Splice_Rec_1928544,Human_Splice_Rec_1928562,Human_Splice_Rec_1928568,Human_Splice_Rec_1928598 GWAS_ID_9600,GWAS_ID_9601 RMVar_hsa_circ_190864,RMVar_hsa_circ_123784 111536 RMVar_ID_111536 Human_SNP_ID_833031501 m1A Human chr19 + 46202887 46202887 46202887 TGAGAAGTTCCTTCGGCTGGGCTGAGGACCCGAGGTCATGGGTGGATCTCATGGAGAGAGGGCGA TGAGAAGTTCCTTCGGCTGGGCTGAGGACCCGGGGTCATGGGTGGATCTCATGGAGAGAGGGCGA A G AC006262.1 Ensembl:ENSG00000268460 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr19:46202823..46202979;chr19:46202791..46203112 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111537 RMVar_ID_111537 Human_SNP_ID_833031807 m1A Human chr19 + 49873135 49873135 49873135 TGTCGTGGAGGCAACGGCGCGCTGCCTCCGCCAGGGCTCCTCGACCATGGGCAGCATAGGCACAG TGTCGTGGAGGCAACGGCGCGCTGCCTCCGCCGGGGCTCCTCGACCATGGGCAGCATAGGCACAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:49873033..49873300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 111538 RMVar_ID_111538 Human_SNP_ID_833033233 m1A Human chr19 + 49004309 49004309 49004309 GCTTCGCAAGGCATGGTGGGTCAGCTGGCGGCACGGCGGGCGGCTGGCGTGGTGCTGGAGATGAT GCTTCGCAAGGCATGGTGGGTCAGCTGGCGGCTCGGCGGGCGGCTGGCGTGGTGCTGGAGATGAT A T RUVBL2 Ensembl:ENSG00000183207 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49003243..49004467 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_54624,Human_RBP_ID_772229,Human_RBP_ID_914967,Human_RBP_ID_3955351,Human_RBP_ID_17935052,Human_RBP_ID_18192392,Human_RBP_ID_18995253,Human_RBP_ID_22446925 Human_Splice_Rec_2028246,Human_Splice_Rec_2028270,Human_Splice_Rec_2028280,Human_Splice_Rec_2028312,Human_Splice_Rec_2028318,Human_Splice_Rec_2028364,Human_Splice_Rec_2028394,Human_Splice_Rec_2028410 Human_miRNA_ID_2398570,Human_miRNA_ID_3011041 RMVar_hsa_circ_97413,RMVar_hsa_circ_102952,RMVar_hsa_circ_195775,RMVar_hsa_circ_99196,RMVar_hsa_circ_195774,RMVar_hsa_circ_87747,RMVar_hsa_circ_119600,RMVar_hsa_circ_195776,RMVar_hsa_circ_195778,RMVar_hsa_circ_91489,RMVar_hsa_circ_195777,RMVar_hsa_circ_85789,RMVar_hsa_circ_195779,RMVar_hsa_circ_318708,RMVar_hsa_circ_195780 111539 RMVar_ID_111539 Human_SNP_ID_833033594 m1A Human chr19 - 49933144 49933144 49933144 GAGGGGTTTGGAATGAAGGTAGAGGCAGGGGGATGAAGGCGCCAGAGCTGAAGACCAGCCCCCAG GAGGGGTTTGGAATGAAGGTAGAGGCAGGGGGGTGAAGGCGCCAGAGCTGAAGACCAGCCCCCAG T C AC011452.2 Ensembl:ENSG00000269179 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49933097..49933197 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - 111540 RMVar_ID_111540 Human_SNP_ID_833034176 m1A Human chr19 + 804397 804397 804397 TGCGCGGCCAGCCCATCTACATCCAGTTCTCCAACCACAAGGAGCTGAAGACCGACAGCTCTCCC TGCGCGGCCAGCCCATCTACATCCAGTTCTCCTACCACAAGGAGCTGAAGACCGACAGCTCTCCC A T PTBP1 Ensembl:ENSG00000011304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:804263..804443 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid medullary_carcinoma 6 head and neck Human_RBP_ID_52502,Human_RBP_ID_9381493,Human_RBP_ID_22812974,Human_RBP_ID_22977100,Human_RBP_ID_26997689,Human_RBP_ID_27280353 Human_Splice_Rec_1928993,Human_Splice_Rec_1929003,Human_Splice_Rec_1929027,Human_Splice_Rec_1929037,Human_Splice_Rec_1929059,Human_Splice_Rec_1929087,Human_Splice_Rec_1929115,Human_Splice_Rec_1929139,Human_Splice_Rec_1929171 Human_miRNA_ID_135150 RMVar_hsa_circ_24441,RMVar_hsa_circ_117637,RMVar_hsa_circ_190902,RMVar_hsa_circ_310732,RMVar_hsa_circ_361069,RMVar_hsa_circ_10537,RMVar_hsa_circ_366009,RMVar_hsa_circ_317702,RMVar_hsa_circ_62801,RMVar_hsa_circ_27836,RMVar_hsa_circ_96776,RMVar_hsa_circ_75523,RMVar_hsa_circ_190904,RMVar_hsa_circ_190905,RMVar_hsa_circ_372992,RMVar_hsa_circ_44569,RMVar_hsa_circ_68621,RMVar_hsa_circ_119201,RMVar_hsa_circ_190906,RMVar_hsa_circ_190907,RMVar_hsa_circ_190908 111541 RMVar_ID_111541 Human_SNP_ID_833034949 m1A Human chr19 + 7926090 7926090 7926090 CGGCGGCGGCGGCCCGGGCTCCGGCTCAGCCCACCCCACCCGCCCCTGGAGCGGCGGAGACCGAG CGGCGGCGGCGGCCCGGGCTCCGGCTCAGCCCCCCCCACCCGCCCCTGGAGCGGCGGAGACCGAG A C AC010336.5 Ensembl:ENSG00000269139 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:7925997..7926112 26863410 MeRIP-seq:(Medium) rs973803640 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111542 RMVar_ID_111542 Human_SNP_ID_833036675 m1A Human chr19 + 47152934 47152932 47152934 GTCTGACTTGCTGCTCCAGGGATGTCATAGTTAAAGTTGACCAGATCTGTCACAAAAATAGCATC GTCTGACTTGCTGCTCCAGGGATGTCATAGT__AAGTTGACCAGATCTGTCACAAAAATAGCATC TTA T SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:47152901..47153000 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 BRCA 1 - Human_RBP_ID_1017311,Human_RBP_ID_1568925,Human_RBP_ID_1890501,Human_RBP_ID_3574387,Human_RBP_ID_4539466,Human_RBP_ID_8490971,Human_RBP_ID_17928570,Human_RBP_ID_18736515,Human_RBP_ID_22236993,Human_RBP_ID_22811425,Human_RBP_ID_27681860 Human_Splice_Rec_2023402,Human_Splice_Rec_2023414,Human_Splice_Rec_2023420,Human_Splice_Rec_2023428,Human_Splice_Rec_2023442,Human_Splice_Rec_2023452,Human_Splice_Rec_2023480,Human_Splice_Rec_2023496,Human_Splice_Rec_2023502,Human_Splice_Rec_2023520,Human_Splice_Rec_2023536,Human_Splice_Rec_2023554,Human_Splice_Rec_2023568 Human_miRNA_ID_1710080,Human_miRNA_ID_2878206,Human_miRNA_ID_3067513 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_338592,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_317076,RMVar_hsa_circ_299077,RMVar_hsa_circ_195560,RMVar_hsa_circ_195561,RMVar_hsa_circ_363271,RMVar_hsa_circ_356999 111543 RMVar_ID_111543 Human_SNP_ID_833038517 m1A Human chr19 + 3983211 3983211 3983211 AGTCGACATGCCCGGGGGAGTCAATGAGGTTGATGAGGAAGCCGGCACCGTCCTTGCTCTGCTTG AGTCGACATGCCCGGGGGAGTCAATGAGGTTGCTGAGGAAGCCGGCACCGTCCTTGCTCTGCTTG A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:3982779..3983337 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111544 RMVar_ID_111544 Human_SNP_ID_833043367 m1A Human chr19 + 11033404 11033404 11033404 TGGAGGAGAAGATCCTAGCTGCAGCCAAGTACAAGCTCAACGTGGACCAGAAGGTGATCCAGGCC TGGAGGAGAAGATCCTAGCTGCAGCCAAGTACGAGCTCAACGTGGACCAGAAGGTGATCCAGGCC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11033354..11033453 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 18 bladder,urinary tract Human_RBP_ID_1879836,Human_RBP_ID_8829482,Human_RBP_ID_9380515,Human_RBP_ID_18191976,Human_RBP_ID_27573098 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_283144,RMVar_hsa_circ_14259,RMVar_hsa_circ_74005,RMVar_hsa_circ_325575,RMVar_hsa_circ_367421,RMVar_hsa_circ_61001 111545 RMVar_ID_111545 Human_SNP_ID_833047641 m1A Human chr19 + 580705 580705 580705 CGTCAGAACACATCAACGAGGGGGAGACGGCCATGCTGGTCTGCAAGTCAGAGTCCGTGCCACCT CGTCAGAACACATCAACGAGGGGGAGACGGCCGTGCTGGTCTGCAAGTCAGAGTCCGTGCCACCT A G BSG Ensembl:ENSG00000172270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:580608..580816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_54537,Human_RBP_ID_240640,Human_RBP_ID_528087,Human_RBP_ID_913665,Human_RBP_ID_4550318,Human_RBP_ID_18192564,Human_RBP_ID_18470337,Human_RBP_ID_22446243,Human_RBP_ID_22762634,Human_RBP_ID_22812634,Human_RBP_ID_26470521,Human_RBP_ID_26996219,Human_RBP_ID_27471884 Human_Splice_Rec_1928468,Human_Splice_Rec_1928469,Human_Splice_Rec_1928480,Human_Splice_Rec_1928481,Human_Splice_Rec_1928496,Human_Splice_Rec_1928497,Human_Splice_Rec_1928504,Human_Splice_Rec_1928505,Human_Splice_Rec_1928536,Human_Splice_Rec_1928537,Human_Splice_Rec_1928550,Human_Splice_Rec_1928551,Human_Splice_Rec_1928554,Human_Splice_Rec_1928555,Human_Splice_Rec_1928574,Human_Splice_Rec_1928575,Human_Splice_Rec_1928586,Human_Splice_Rec_1928590,Human_Splice_Rec_1928591 Human_miRNA_ID_2442303,Human_miRNA_ID_2442304 RMVar_hsa_circ_10111,RMVar_hsa_circ_111780,RMVar_hsa_circ_120957,RMVar_hsa_circ_190861,RMVar_hsa_circ_190862,RMVar_hsa_circ_373981,RMVar_hsa_circ_190864,RMVar_hsa_circ_123784,RMVar_hsa_circ_190863 111546 RMVar_ID_111546 Human_SNP_ID_833047979 m1A Human chr19 - 1074437 1074437 1074437 AATGGGGCTGAGACTCACACCCGGGCCCAGGGACCCCCGCCCCGTGCCCGCGGGGCCCCCACCTC AATGGGGCTGAGACTCACACCCGGGCCCAGGGCCCCCCGCCCCGTGCCCGCGGGGCCCCCACCTC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:1074426..1074450 26863196 MeRIP-seq:(Medium) rs942226123 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111547 RMVar_ID_111547 Human_SNP_ID_833049572 m1A Human chr19 - 49869318 49869318 49869318 TCCCGACAACTTGTTCCCTGACCCCCTCAGGGATGGCCCCAAACTGTCCCTGCCTCTGGCACCCC TCCCGACAACTTGTTCCCTGACCCCCTCAGGGGTGGCCCCAAACTGTCCCTGCCTCTGGCACCCC T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49869267..49869363 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_525676,Human_RBP_ID_1017619,Human_RBP_ID_5116396,Human_RBP_ID_17083342,Human_RBP_ID_17385170,Human_RBP_ID_17501211,Human_RBP_ID_17657311,Human_RBP_ID_17929606,Human_RBP_ID_18945884,Human_RBP_ID_24484750 Human_miRNA_ID_444780,Human_miRNA_ID_1267624,Human_miRNA_ID_1973898,Human_miRNA_ID_1976077,Human_miRNA_ID_2613868,Human_miRNA_ID_3002194 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 111548 RMVar_ID_111548 Human_SNP_ID_833055026 m1A Human chr19 + 42233290 42233290 42233290 CCCTGCCCAGCCCAGCCCCGCCCCTCACCTTGATGATCTCCACCAGCTGGTCCACCCCACTGTCC CCCTGCCCAGCCCAGCCCCGCCCCTCACCTTGGTGATCTCCACCAGCTGGTCCACCCCACTGTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42232813..42234621 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 111549 RMVar_ID_111549 Human_SNP_ID_833057685 m1A Human chr19 + 4695502 4695499 4695502 TCTCTGTGCTCGGGATGAACAGGGCCGGGGGGAGGAGGACGAGCTGGAGCCACTGCTGGGGCCGG TCTCTGTGCTCGGGATGAACAGGGCCGGGG___GGAGGACGAGCTGGAGCCACTGCTGGGGCCGG GGGA G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4695384..4695525 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 COCA 1 - 111550 RMVar_ID_111550 Human_SNP_ID_833059950 m1A Human chr19 + 18575134 18575132 18575135 GAAGTGTGGTCACACCAACAACCTGCGTCCCAAGAAGAAGGTCAAATAAGGTGGTTCTTTCCTTG GAAGTGTGGTCACACCAACAACCTGCGTCCC___AAGAAGGTCAAATAAGGTGGTTCTTTCCTTG CAAG C UBA52 Ensembl:ENSG00000221983 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:18575009..18575250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 HNSC 1 - Human_RBP_ID_516356,Human_RBP_ID_825215,Human_RBP_ID_912813,Human_RBP_ID_1556544,Human_RBP_ID_1881229,Human_RBP_ID_3564618,Human_RBP_ID_4510844,Human_RBP_ID_8479898,Human_RBP_ID_9085068,Human_RBP_ID_17267175,Human_RBP_ID_17502429,Human_RBP_ID_17656036,Human_RBP_ID_18192143,Human_RBP_ID_22449311,Human_RBP_ID_23786776,Human_RBP_ID_26466111,Human_RBP_ID_26817295,Human_RBP_ID_26985508,Human_RBP_ID_27270294 Human_Splice_Rec_1980714,Human_Splice_Rec_1980722,Human_Splice_Rec_1980730,Human_Splice_Rec_1980738,Human_Splice_Rec_1980748,Human_Splice_Rec_1980758,Human_Splice_Rec_1980766,Human_Splice_Rec_1980774,Human_Splice_Rec_1980780,Human_Splice_Rec_1980786,Human_Splice_Rec_1980787,Human_Splice_Rec_1980798 RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_75863,RMVar_hsa_circ_193499,RMVar_hsa_circ_88418,RMVar_hsa_circ_326866,RMVar_hsa_circ_98132,RMVar_hsa_circ_193507,RMVar_hsa_circ_193508 111551 RMVar_ID_111551 Human_SNP_ID_833061337 m1A Human chr19 + 58477325 58477325 58477325 CCGCCTCCGCTTCCGAGGGTTCTGCTACCAGGAGGTGGCAGGTCCCCGAGAAGCCCTGGCCCGGC CCGCCTCCGCTTCCGAGGGTTCTGCTACCAGGGGGTGGCAGGTCCCCGAGAAGCCCTGGCCCGGC A G ZNF446 Ensembl:ENSG00000083838 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58477275..58477425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine 111552 RMVar_ID_111552 Human_SNP_ID_833061783 m1A Human chr19 + 44973162 44973162 44973162 CCGGCCCCTCAGGACCAGGCGGGCCCCGGAGGAGCTCCACGCGTCGCCAGCCGCAACCTGTTCCC CCGGCCCCTCAGGACCAGGCGGGCCCCGGAGGGGCTCCACGCGTCGCCAGCCGCAACCTGTTCCC A G CLPTM1 Ensembl:ENSG00000104853 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44973040..44973256 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_8427,Human_RBP_ID_239463,Human_RBP_ID_1294970,Human_RBP_ID_22447867,Human_RBP_ID_26468925 Human_Splice_Rec_2018068,Human_Splice_Rec_2018069,Human_Splice_Rec_2018082,Human_Splice_Rec_2018083,Human_Splice_Rec_2018106,Human_Splice_Rec_2018107,Human_Splice_Rec_2018132,Human_Splice_Rec_2018133,Human_Splice_Rec_2018158,Human_Splice_Rec_2018159,Human_Splice_Rec_2018166,Human_Splice_Rec_2018167 RMVar_hsa_circ_7756,RMVar_hsa_circ_59809,RMVar_hsa_circ_374212,RMVar_hsa_circ_57961,RMVar_hsa_circ_320125,RMVar_hsa_circ_195257,RMVar_hsa_circ_195258 111553 RMVar_ID_111553 Human_SNP_ID_833063898 m1A Human chr19 - 14529651 14529651 14529651 GGCGGCTACTGCTCCGCGGCTGCTGCTGCCTAACTGCGCGGCACAGCACAGGCTCCCTACAGCGC GGCGGCTACTGCTCCGCGGCTGCTGCTGCCTATCTGCGCGGCACAGCACAGGCTCCCTACAGCGC T A DNAJB1 Ensembl:ENSG00000132002 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:14529576..14529770;chr19:14529576..14529783 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 111554 RMVar_ID_111554 Human_SNP_ID_833064389 m1A Human chr19 + 17276504 17276504 17276504 GCTCCCTCCTCCCGGGTATGCAGCCAGCAGAAAACTGAGCTTCCGGTCACAGAGAACGTGCAGAC GCTCCCTCCTCCCGGGTATGCAGCCAGCAGAACACTGAGCTTCCGGTCACAGAGAACGTGCAGAC A C AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17276501..17276625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_515595,Human_RBP_ID_907521,Human_RBP_ID_1013626,Human_RBP_ID_18724253,Human_RBP_ID_22665096 Human_Splice_Rec_1976078,Human_Splice_Rec_1976092,Human_Splice_Rec_1976110,Human_Splice_Rec_1976126,Human_Splice_Rec_1976140,Human_Splice_Rec_1976152,Human_Splice_Rec_1976168,Human_Splice_Rec_1976194,Human_Splice_Rec_1976212,Human_Splice_Rec_1976218,Human_Splice_Rec_1976234,Human_Splice_Rec_1976244,Human_Splice_Rec_1976266 RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_322263,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_111991,RMVar_hsa_circ_115721,RMVar_hsa_circ_295755,RMVar_hsa_circ_193297,RMVar_hsa_circ_270986,RMVar_hsa_circ_193298,RMVar_hsa_circ_193299 111555 RMVar_ID_111555 Human_SNP_ID_833067962 m1A Human chr19 + 11033366 11033366 11033366 CGAGGTGCGTGTGCTCCGCCTCTGCACCGTCAACAGCGTGGAGGAGAAGATCCTAGCTGCAGCCA CGAGGTGCGTGTGCTCCGCCTCTGCACCGTCAGCAGCGTGGAGGAGAAGATCCTAGCTGCAGCCA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11033276..11033400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 18 head and neck Human_RBP_ID_53734,Human_RBP_ID_1879836,Human_RBP_ID_9380515,Human_RBP_ID_18191976 Human_Splice_Rec_1956914,Human_Splice_Rec_1956982,Human_Splice_Rec_1957048,Human_Splice_Rec_1957118,Human_Splice_Rec_1957186,Human_Splice_Rec_1957252,Human_Splice_Rec_1957316,Human_Splice_Rec_1957384,Human_Splice_Rec_1957448,Human_Splice_Rec_1957516,Human_Splice_Rec_1957584,Human_Splice_Rec_1957660,Human_Splice_Rec_1957728,Human_Splice_Rec_1957794,Human_Splice_Rec_1957860,Human_Splice_Rec_1957926,Human_Splice_Rec_1957992,Human_Splice_Rec_1958054,Human_Splice_Rec_1958164,Human_Splice_Rec_1958218,Human_Splice_Rec_1958272,Human_Splice_Rec_1958322,Human_Splice_Rec_1958372,Human_Splice_Rec_1958424,Human_Splice_Rec_1958474,Human_Splice_Rec_1958556,Human_Splice_Rec_1958604,Human_Splice_Rec_1958644,Human_Splice_Rec_1958690,Human_Splice_Rec_1958740,Human_Splice_Rec_1958790,Human_Splice_Rec_1958852,Human_Splice_Rec_1958892,Human_Splice_Rec_1958930,Human_Splice_Rec_1958974,Human_Splice_Rec_1959006,Human_Splice_Rec_1959028,Human_Splice_Rec_1959056,Human_Splice_Rec_1959078 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_283144,RMVar_hsa_circ_14259,RMVar_hsa_circ_74005,RMVar_hsa_circ_325575,RMVar_hsa_circ_367421,RMVar_hsa_circ_61001 111556 RMVar_ID_111556 Human_SNP_ID_833067990 m1A Human chr19 + 11033366 11033366 11033366 CGAGGTGCGTGTGCTCCGCCTCTGCACCGTCAACAGCGTGGAGGAGAAGATCCTAGCTGCAGCCA CGAGGTGCGTGTGCTCCGCCTCTGCACCGTCACCAGCGTGGAGGAGAAGATCCTAGCTGCAGCCA A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11033276..11033400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_53734,Human_RBP_ID_1879836,Human_RBP_ID_9380515,Human_RBP_ID_18191976 Human_Splice_Rec_1956914,Human_Splice_Rec_1956982,Human_Splice_Rec_1957048,Human_Splice_Rec_1957118,Human_Splice_Rec_1957186,Human_Splice_Rec_1957252,Human_Splice_Rec_1957316,Human_Splice_Rec_1957384,Human_Splice_Rec_1957448,Human_Splice_Rec_1957516,Human_Splice_Rec_1957584,Human_Splice_Rec_1957660,Human_Splice_Rec_1957728,Human_Splice_Rec_1957794,Human_Splice_Rec_1957860,Human_Splice_Rec_1957926,Human_Splice_Rec_1957992,Human_Splice_Rec_1958054,Human_Splice_Rec_1958164,Human_Splice_Rec_1958218,Human_Splice_Rec_1958272,Human_Splice_Rec_1958322,Human_Splice_Rec_1958372,Human_Splice_Rec_1958424,Human_Splice_Rec_1958474,Human_Splice_Rec_1958556,Human_Splice_Rec_1958604,Human_Splice_Rec_1958644,Human_Splice_Rec_1958690,Human_Splice_Rec_1958740,Human_Splice_Rec_1958790,Human_Splice_Rec_1958852,Human_Splice_Rec_1958892,Human_Splice_Rec_1958930,Human_Splice_Rec_1958974,Human_Splice_Rec_1959006,Human_Splice_Rec_1959028,Human_Splice_Rec_1959056,Human_Splice_Rec_1959078 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_283144,RMVar_hsa_circ_14259,RMVar_hsa_circ_74005,RMVar_hsa_circ_325575,RMVar_hsa_circ_367421,RMVar_hsa_circ_61001 111557 RMVar_ID_111557 Human_SNP_ID_833069011 m1A Human chr19 - 10991263 10991263 10991263 TGCTCGATCTTCTGCTGCTTCTCCAGCTTCTCAGTGATGCGGGCCTCGCGCAGGGACTGGCGCTT TGCTCGATCTTCTGCTGCTTCTCCAGCTTCTCGGTGATGCGGGCCTCGCGCAGGGACTGGCGCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10991213..10991366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 20 uterus 111558 RMVar_ID_111558 Human_SNP_ID_833073523 m1A Human chr19 - 2111798 2111798 2111798 AGAAATCTCCCAAGCCTAAGAAGAAGAAGCACAGGAAGGAGAAGGAGGAGCGGACCAAAGGCAAG AGAAATCTCCCAAGCCTAAGAAGAAGAAGCACGGGAAGGAGAAGGAGGAGCGGACCAAAGGCAAG T C AP3D1 Ensembl:ENSG00000065000 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2111647..2111865 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_52665,Human_RBP_ID_910084,Human_RBP_ID_1881530,Human_RBP_ID_4564615,Human_RBP_ID_9379996,Human_RBP_ID_22810069,Human_RBP_ID_22977332,Human_RBP_ID_24545379,Human_RBP_ID_26335084,Human_RBP_ID_26986489,Human_RBP_ID_27814878 Human_Splice_Rec_1934878,Human_Splice_Rec_1934936,Human_Splice_Rec_1935000,Human_Splice_Rec_1935052 RMVar_hsa_circ_24503,RMVar_hsa_circ_104689,RMVar_hsa_circ_103350,RMVar_hsa_circ_80576,RMVar_hsa_circ_114869,RMVar_hsa_circ_191145,RMVar_hsa_circ_191146,RMVar_hsa_circ_191147,RMVar_hsa_circ_107745,RMVar_hsa_circ_61263,RMVar_hsa_circ_191148,RMVar_hsa_circ_88060,RMVar_hsa_circ_98523,RMVar_hsa_circ_191150,RMVar_hsa_circ_191151,RMVar_hsa_circ_265929,RMVar_hsa_circ_191152 111559 RMVar_ID_111559 Human_SNP_ID_833080480 m1A Human chr19 - 15256080 15256080 15256080 CTCCTCCTAAAAAGACGAAGAAAAATAATAGCAGCAACAGCAATGTGAGGTCTGTGTCCCCTGAA CTCCTCCTAAAAAGACGAAGAAAAATAATAGCCGCAACAGCAATGTGAGGTCTGTGTCCCCTGAA T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:15255330..15256215 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_910819,Human_RBP_ID_9380700,Human_RBP_ID_18412503,Human_RBP_ID_18532279,Human_RBP_ID_22230426,Human_RBP_ID_24545455,Human_RBP_ID_26335905,Human_RBP_ID_27815237 Human_Splice_Rec_1970619,Human_Splice_Rec_1970657,Human_Splice_Rec_1970679 Human_miRNA_ID_2022900,Human_miRNA_ID_2261440,Human_miRNA_ID_2264488,Human_miRNA_ID_2267554 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 111560 RMVar_ID_111560 Human_SNP_ID_833081946 m1A Human chr19 + 12943782 12943782 12943782 AGCAGAGGCTTAAGGAGGAGGAAGAAGACAAGAAACGCAAAGAGGAGGAGGAGGCAGAGGACAAG AGCAGAGGCTTAAGGAGGAGGAAGAAGACAAGGAACGCAAAGAGGAGGAGGAGGCAGAGGACAAG A G CALR Ensembl:ENSG00000179218 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:12943576..12944075;chr19:12943576..12944385 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue myelofibrosis 1 haematopoietic and lymphoid tissue Human_RBP_ID_825947,Human_RBP_ID_1880272,Human_RBP_ID_2556494,Human_RBP_ID_5116727,Human_RBP_ID_5585366,Human_RBP_ID_6721337,Human_RBP_ID_9380617,Human_RBP_ID_13372465,Human_RBP_ID_22391076,Human_RBP_ID_22966984,Human_RBP_ID_23783075,Human_RBP_ID_24545579,Human_RBP_ID_24552816,Human_RBP_ID_26335807,Human_RBP_ID_26983149,Human_RBP_ID_27463687,Human_RBP_ID_27815187 Human_Splice_Rec_1964392,Human_Splice_Rec_1964416,Human_Splice_Rec_1964418 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_110485,RMVar_hsa_circ_192843,RMVar_hsa_circ_192844,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_81328,RMVar_hsa_circ_192849,RMVar_hsa_circ_192851,RMVar_hsa_circ_76392,RMVar_hsa_circ_192853,RMVar_hsa_circ_192854,RMVar_hsa_circ_110866,RMVar_hsa_circ_192855,RMVar_hsa_circ_378042 111561 RMVar_ID_111561 Human_SNP_ID_833088907 m1A Human chr19 - 47094480 47094478 47094481 GGGGGAGAAGCATCACAGTGATTCGGATGAGGAGAAGTCCCACAGGAGACTGAAGCGGAAACGGA GGGGGAGAAGCATCACAGTGATTCGGATGAG___AAGTCCCACAGGAGACTGAAGCGGAAACGGA TCTC T ZC3H4 Ensembl:ENSG00000130749 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47094365..47094575 26863196 MeRIP-seq:(Medium) rs748255221 Functional Loss DEL TCGA,ICGC 32..34 33 PRAD,STAD 2 - Human_RBP_ID_54035,Human_RBP_ID_911661,Human_RBP_ID_4539382,Human_RBP_ID_8835964,Human_RBP_ID_9381210,Human_RBP_ID_13482512,Human_RBP_ID_17928548,Human_RBP_ID_18441703,Human_RBP_ID_18532573,Human_RBP_ID_26338031,Human_RBP_ID_27815519 Human_Splice_Rec_2023343,Human_Splice_Rec_2023377,Human_Splice_Rec_2023389,Human_Splice_Rec_2023393 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_58958,RMVar_hsa_circ_2929,RMVar_hsa_circ_70973,RMVar_hsa_circ_195550,RMVar_hsa_circ_63333,RMVar_hsa_circ_40571,RMVar_hsa_circ_195555,RMVar_hsa_circ_345662,RMVar_hsa_circ_105192 111562 RMVar_ID_111562 Human_SNP_ID_833093483 m1A Human chr19 + 58556340 58556340 58556340 CTACTCACCAAGAAGAGATACTGCAGGCCATAAATTATGGAGTTTATCGTAAGGACTGGCTTCCA CTACTCACCAAGAAGAGATACTGCAGGCCATACATTATGGAGTTTATCGTAAGGACTGGCTTCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:58556326..58556350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - 111563 RMVar_ID_111563 Human_SNP_ID_833093691 m1A Human chr19 - 35277165 35277165 35277165 GTGCGCTGAACCTTCCCACCAAAGACAACCACACCCGCCTTTGGGAACTCTGGCCAAAAGCAGCA GTGCGCTGAACCTTCCCACCAAAGACAACCACCCCCGCCTTTGGGAACTCTGGCCAAAAGCAGCA T G lnc-FAM187B-3 RNACentral:URS00009BF8ED lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:35277158..35277511;chr19:35277160..35277428 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary 111564 RMVar_ID_111564 Human_SNP_ID_833096587 m1A Human chr19 + 39391577 39391577 39391577 TGCCCAGAGCGGCCTCCTGCAGCAACAGCAACAGGACTTCGATCCTGTGCAGCGTTATAAGATGC TGCCCAGAGCGGCCTCCTGCAGCAACAGCAACGGGACTTCGATCCTGTGCAGCGTTATAAGATGC A G MED29 Ensembl:ENSG00000063322 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:39391526..39391600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4527523 Human_Splice_Rec_2005553,Human_Splice_Rec_2005557,Human_Splice_Rec_2005563,Human_Splice_Rec_2005569,Human_Splice_Rec_2005575,Human_Splice_Rec_2005581 111565 RMVar_ID_111565 Human_SNP_ID_833100446 m1A Human chr19 - 49449643 49449643 49449643 TGACTAACCCACTCCCACCAGGTTTCTGCATAAAGACCAACTCCTCGGAAGGGAAGGTTTTCATC TGACTAACCCACTCCCACCAGGTTTCTGCATAGAGACCAACTCCTCGGAAGGGAAGGTTTTCATC T C PIH1D1 Ensembl:ENSG00000104872 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49449634..49449749 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 2 breast Human_RBP_ID_4571836,Human_RBP_ID_26817837 Human_Splice_Rec_2030100,Human_Splice_Rec_2030114,Human_Splice_Rec_2030212,Human_Splice_Rec_2030228,Human_Splice_Rec_2030244,Human_Splice_Rec_2030258,Human_Splice_Rec_2030270,Human_Splice_Rec_2030282,Human_Splice_Rec_2030292,Human_Splice_Rec_2030300,Human_Splice_Rec_2030304,Human_Splice_Rec_2030310 RMVar_hsa_circ_96360,RMVar_hsa_circ_195834,RMVar_hsa_circ_74117,RMVar_hsa_circ_7003,RMVar_hsa_circ_75727,RMVar_hsa_circ_113228,RMVar_hsa_circ_81002,RMVar_hsa_circ_195839,RMVar_hsa_circ_195840,RMVar_hsa_circ_195841,RMVar_hsa_circ_117349,RMVar_hsa_circ_297276,RMVar_hsa_circ_195842,RMVar_hsa_circ_195843 111566 RMVar_ID_111566 Human_SNP_ID_833100447 m1A Human chr19 - 49449643 49449643 49449643 TGACTAACCCACTCCCACCAGGTTTCTGCATAAAGACCAACTCCTCGGAAGGGAAGGTTTTCATC TGACTAACCCACTCCCACCAGGTTTCTGCATATAGACCAACTCCTCGGAAGGGAAGGTTTTCATC T A PIH1D1 Ensembl:ENSG00000104872 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49449634..49449749 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_4571836,Human_RBP_ID_26817837 Human_Splice_Rec_2030100,Human_Splice_Rec_2030114,Human_Splice_Rec_2030212,Human_Splice_Rec_2030228,Human_Splice_Rec_2030244,Human_Splice_Rec_2030258,Human_Splice_Rec_2030270,Human_Splice_Rec_2030282,Human_Splice_Rec_2030292,Human_Splice_Rec_2030300,Human_Splice_Rec_2030304,Human_Splice_Rec_2030310 RMVar_hsa_circ_96360,RMVar_hsa_circ_195834,RMVar_hsa_circ_74117,RMVar_hsa_circ_7003,RMVar_hsa_circ_75727,RMVar_hsa_circ_113228,RMVar_hsa_circ_81002,RMVar_hsa_circ_195839,RMVar_hsa_circ_195840,RMVar_hsa_circ_195841,RMVar_hsa_circ_117349,RMVar_hsa_circ_297276,RMVar_hsa_circ_195842,RMVar_hsa_circ_195843 111567 RMVar_ID_111567 Human_SNP_ID_833104776 m1A Human chr19 - 6420146 6420146 6420146 CACGCTTTGCTTTTCTCCTTCTTTCTCCATCCAGTCATTGGCAGAGGAGGTGAACAAATTAACAA CACGCTTTGCTTTTCTCCTTCTTTCTCCATCCGGTCATTGGCAGAGGAGGTGAACAAATTAACAA T C KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6420031..6420506 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach Human_RBP_ID_52809,Human_RBP_ID_1574282,Human_RBP_ID_9090429,Human_RBP_ID_13531646,Human_RBP_ID_20427569,Human_RBP_ID_22005505,Human_RBP_ID_24559809,Human_RBP_ID_25438139 Human_Splice_Rec_1944551,Human_Splice_Rec_1944591,Human_Splice_Rec_1944647,Human_Splice_Rec_1944685,Human_Splice_Rec_1944701 RMVar_hsa_circ_11722,RMVar_hsa_circ_16929,RMVar_hsa_circ_114390,RMVar_hsa_circ_191824,RMVar_hsa_circ_339759,RMVar_hsa_circ_47098,RMVar_hsa_circ_23523,RMVar_hsa_circ_58290 111568 RMVar_ID_111568 Human_SNP_ID_833109492 m1A Human chr19 - 868930 868930 868930 TCCCCTCTCCCGCCAGGGCCCCAGGCCAGCCCAAGATCGACCACCTGCGGAGGCTGCACCTTGGC TCCCCTCTCCCGCCAGGGCCCCAGGCCAGCCCGAGATCGACCACCTGCGGAGGCTGCACCTTGGC T C MED16 Ensembl:ENSG00000175221 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868923..869272 26863196 MeRIP-seq:(Medium) rs754553007 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_22661422 Human_Splice_Rec_1929348,Human_Splice_Rec_1929349,Human_Splice_Rec_1929376,Human_Splice_Rec_1929377,Human_Splice_Rec_1929380,Human_Splice_Rec_1929381,Human_Splice_Rec_1929400,Human_Splice_Rec_1929401,Human_Splice_Rec_1929428,Human_Splice_Rec_1929429,Human_Splice_Rec_1929441,Human_Splice_Rec_1929470,Human_Splice_Rec_1929471 RMVar_hsa_circ_94288,RMVar_hsa_circ_78081,RMVar_hsa_circ_190922,RMVar_hsa_circ_190923 111569 RMVar_ID_111569 Human_SNP_ID_833111424 m1A Human chr19 - 43527075 43527075 43527075 TCCTGCGGCAGGTGCGGGTGGCTGGACCTAGGAGGGGACTGCTGGGCACTAGGCGGCAGCAAGGA TCCTGCGGCAGGTGCGGGTGGCTGGACCTAGGGGGGGACTGCTGGGCACTAGGCGGCAGCAAGGA T C ETHE1 Ensembl:ENSG00000105755 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:43527072..43527159 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_914788 RMVar_hsa_circ_8764,RMVar_hsa_circ_122257,RMVar_hsa_circ_195145 111570 RMVar_ID_111570 Human_SNP_ID_833112784 m1A Human chr19 + 6454648 6454648 6454648 TGCCACTGCGCCGGCCACCAGCTGTTTCCACCACATGCCCGTCAGCTTCTCTTGCTTTGAGAACT TGCCACTGCGCCGGCCACCAGCTGTTTCCACCCCATGCCCGTCAGCTTCTCTTGCTTTGAGAACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6454598..6454705 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck 111571 RMVar_ID_111571 Human_SNP_ID_833114840 m1A Human chr19 - 49818341 49818341 49818341 GCGCGGGCCGGGCCCTCGGACCCGGGGACCATACCCCGTGCGGTACCCGCCACCACCACTGCAGC GCGCGGGCCGGGCCCTCGGACCCGGGGACCATCCCCCGTGCGGTACCCGCCACCACCACTGCAGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49818276..49818573 26863196 MeRIP-seq:(Medium) rs756977834 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary 111572 RMVar_ID_111572 Human_SNP_ID_833122445 m1A Human chr19 + 52225770 52225770 52225770 GCCCATCCTAGAGAAGCTGACCCAGGACCAGGATGTGGACGTCAAATACTTTGCCCAGGAGGCTC GCCCATCCTAGAGAAGCTGACCCAGGACCAGGGTGTGGACGTCAAATACTTTGCCCAGGAGGCTC A G PPP2R1A Ensembl:ENSG00000105568 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:52225684..52225835 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 2 uterus Human_RBP_ID_526273,Human_RBP_ID_1017899,Human_RBP_ID_1570501,Human_RBP_ID_1891411,Human_RBP_ID_3575820,Human_RBP_ID_3955507,Human_RBP_ID_6781582,Human_RBP_ID_8493050,Human_RBP_ID_8836853,Human_RBP_ID_9293935,Human_RBP_ID_13504286,Human_RBP_ID_17270455,Human_RBP_ID_17501330,Human_RBP_ID_17930317,Human_RBP_ID_18738544,Human_RBP_ID_18995385,Human_RBP_ID_26816290,Human_RBP_ID_26994743,Human_RBP_ID_27157849 Human_Splice_Rec_2039282,Human_Splice_Rec_2039283,Human_Splice_Rec_2039320,Human_Splice_Rec_2039321,Human_Splice_Rec_2039350 RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_127662,RMVar_hsa_circ_127787,RMVar_hsa_circ_97176,RMVar_hsa_circ_196085,RMVar_hsa_circ_196084,RMVar_hsa_circ_372981,RMVar_hsa_circ_122127,RMVar_hsa_circ_196092,RMVar_hsa_circ_196093,RMVar_hsa_circ_122250,RMVar_hsa_circ_196094,RMVar_hsa_circ_196096,RMVar_hsa_circ_196102,RMVar_hsa_circ_279840,RMVar_hsa_circ_126910,RMVar_hsa_circ_77928,RMVar_hsa_circ_196104,RMVar_hsa_circ_324394,RMVar_hsa_circ_196105,RMVar_hsa_circ_196106,RMVar_hsa_circ_196109,RMVar_hsa_circ_112824,RMVar_hsa_circ_292359,RMVar_hsa_circ_370226,RMVar_hsa_circ_196108,RMVar_hsa_circ_196110 111573 RMVar_ID_111573 Human_SNP_ID_833125049 m1A Human chr19 - 282216 282216 282216 CTTCCTGGTGGCCTTTGCCCTCTACGTGGGCTACACCCGCGTGTCTGATTACAAACACCACTGGA CTTCCTGGTGGCCTTTGCCCTCTACGTGGGCTGCACCCGCGTGTCTGATTACAAACACCACTGGA T C PLPP2 Ensembl:ENSG00000141934 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:282126..282250 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_Splice_Rec_1928086,Human_Splice_Rec_1928087,Human_Splice_Rec_1928096,Human_Splice_Rec_1928097,Human_Splice_Rec_1928106,Human_Splice_Rec_1928107,Human_Splice_Rec_1928110,Human_Splice_Rec_1928111,Human_Splice_Rec_1928120,Human_Splice_Rec_1928121,Human_Splice_Rec_1928126 111574 RMVar_ID_111574 Human_SNP_ID_833125189 m1A Human chr19 - 3538485 3538482 3538485 GAAATGTCCAGGACAGACCAATCCACAGAATCAGGGAGAGGATTCGTGGGTGCCGGGACTGGGGA GAAATGTCCAGGACAGACCAATCCACAGAATC___GAGAGGATTCGTGGGTGCCGGGACTGGGGA CCCT C MFSD12 Ensembl:ENSG00000161091 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3538476..3538525 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..35 33 SKCA 1 - Human_RBP_ID_55458,Human_RBP_ID_519787,Human_RBP_ID_26335169 Human_miRNA_ID_120325,Human_miRNA_ID_124140 111575 RMVar_ID_111575 Human_SNP_ID_833125980 m1A Human chr19 - 12925141 12925139 12925141 TCCAGCGGAGGCCCTGCAGCTCCCAATGGACTATGTCCAGCGGGTCAAGCGGACCCACTCTCAGG TCCAGCGGAGGCCCTGCAGCTCCCAATGGACT__GTCCAGCGGGTCAAGCGGACCCACTCTCAGG CAT C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:12925076..12925150 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_772168,Human_RBP_ID_4562134,Human_RBP_ID_22446483,Human_RBP_ID_25384480,Human_RBP_ID_26983105 Human_Splice_Rec_1964216,Human_Splice_Rec_1964217,Human_Splice_Rec_1964242,Human_Splice_Rec_1964243,Human_Splice_Rec_1964264,Human_Splice_Rec_1964265,Human_Splice_Rec_1964288,Human_Splice_Rec_1964289,Human_Splice_Rec_1964312,Human_Splice_Rec_1964313,Human_Splice_Rec_1964322,Human_Splice_Rec_1964323,Human_Splice_Rec_1964336,Human_Splice_Rec_1964337 RMVar_hsa_circ_109494,RMVar_hsa_circ_192819,RMVar_hsa_circ_77885,RMVar_hsa_circ_114698,RMVar_hsa_circ_326312,RMVar_hsa_circ_192820,RMVar_hsa_circ_98841,RMVar_hsa_circ_192822,RMVar_hsa_circ_106605,RMVar_hsa_circ_192821,RMVar_hsa_circ_82781,RMVar_hsa_circ_192826,RMVar_hsa_circ_85645,RMVar_hsa_circ_192823,RMVar_hsa_circ_192824,RMVar_hsa_circ_378140,RMVar_hsa_circ_192827 111576 RMVar_ID_111576 Human_SNP_ID_833127502 m1A Human chr19 - 5664074 5664074 5664074 GAAGCGGTCCTGGCGGTTAAAGTCAGAATGGTAGCGCTCATCCAGGGCGGCCCGCTTGGCTTCCG GAAGCGGTCCTGGCGGTTAAAGTCAGAATGGTGGCGCTCATCCAGGGCGGCCCGCTTGGCTTCCG T C RF00017-1299 RNACentral:URS000098668F SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5663977..5664234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney 111577 RMVar_ID_111577 Human_SNP_ID_833129240 m1A Human chr19 - 36141158 36141158 36141158 CGCATGGCCGTTCCACCGCCACCGCCGCCTCCACCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC CGCATGGCCGTTCCACCGCCACCGCCGCCTCCTCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEK293T,Wild Type;HEK293T,H2O2 treatment;HEK293T,untreat control chr19:36140976..36141302;chr19:36140976..36141339;chr19:36141001..36141236;chr19:36141058..36141158;chr19:36141046..36141250 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs11084845 Functional Loss SNV ICGC 33..33 33 COCA 1 - 111578 RMVar_ID_111578 Human_SNP_ID_833130616 m1A Human chr19 + 3983115 3983115 3983115 CGTGCCTCAGGGGGACCCACTGCTTACCTGACACGCAGTCCACCACCACCAATGCGCCATCGGTG CGTGCCTCAGGGGGACCCACTGCTTACCTGACGCGCAGTCCACCACCACCAATGCGCCATCGGTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3982789..3983118 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 111579 RMVar_ID_111579 Human_SNP_ID_833136104 m1A Human chr19 + 49108002 49108002 49108002 AGCAAGGACAAGGACCGGGACCGGAAGCGGCGAAGCAGCCGGAGTCGGGAGCGGGCCCGGCGGGA AGCAAGGACAAGGACCGGGACCGGAAGCGGCGGAGCAGCCGGAGTCGGGAGCGGGCCCGGCGGGA A G SNRNP70 Ensembl:ENSG00000104852 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_22977933 111580 RMVar_ID_111580 Human_SNP_ID_833136189 m1A Human chr19 + 18427932 18427932 18427932 TCTTCTGGGACCTGTACTGCGCGGCGCCTGACAGAAGAGAGGCCTGCGAGCACTCCGGCGAGGCC TCTTCTGGGACCTGTACTGCGCGGCGCCTGACCGAAGAGAGGCCTGCGAGCACTCCGGCGAGGCC A C SSBP4 Ensembl:ENSG00000130511 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18427797..18428022 26863196 MeRIP-seq:(Medium) rs10405636 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 7 head and neck,large intestine Human_Splice_Rec_1980004,Human_Splice_Rec_1980005,Human_Splice_Rec_1980020,Human_Splice_Rec_1980021,Human_Splice_Rec_1980052,Human_Splice_Rec_1980053,Human_Splice_Rec_1980086,Human_Splice_Rec_1980087,Human_Splice_Rec_1980098,Human_Splice_Rec_1980099,Human_Splice_Rec_1980110,Human_Splice_Rec_1980111,Human_Splice_Rec_1980126,Human_Splice_Rec_1980127,Human_Splice_Rec_1980138,Human_Splice_Rec_1980139,Human_Splice_Rec_1980156,Human_Splice_Rec_1980157 GWAS_ID_6625,GWAS_ID_6626,GWAS_ID_6627,GWAS_ID_6628,GWAS_ID_6629,GWAS_ID_6630 RMVar_hsa_circ_82466,RMVar_hsa_circ_193469 111581 RMVar_ID_111581 Human_SNP_ID_833142470 m1A Human chr19 + 49712821 49712821 49712821 GCATCTGTTTGACGTCCACAATTACCCGGACTATGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA GCATCTGTTTGACGTCCACAATTACCCGGACTGTGTTTCCTCAGGCGGTGGATTCGGGCCTGTGA A G CPT1C Ensembl:ENSG00000169169 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49712733..49712834 26863410 MeRIP-seq:(Medium) rs1161252718 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 13 pancreas Human_RBP_ID_1017580 Human_Splice_Rec_2031908,Human_Splice_Rec_2031909,Human_Splice_Rec_2031948,Human_Splice_Rec_2031949,Human_Splice_Rec_2032010,Human_Splice_Rec_2032011,Human_Splice_Rec_2032062,Human_Splice_Rec_2032063,Human_Splice_Rec_2032106,Human_Splice_Rec_2032107,Human_Splice_Rec_2032222,Human_Splice_Rec_2032223,Human_Splice_Rec_2032227,Human_Splice_Rec_2032231 RMVar_hsa_circ_195924,RMVar_hsa_circ_123917,RMVar_hsa_circ_367328,RMVar_hsa_circ_195925,RMVar_hsa_circ_78674,RMVar_hsa_circ_195929,RMVar_hsa_circ_195935 111582 RMVar_ID_111582 Human_SNP_ID_833145194 m1A Human chr19 + 46738830 46738830 46738830 GCGCATACTCTAGCATCTTGATCCGCCGCACCAGGTCCGTCTTTAGATTCTCCTGCCCTTTCCTC GCGCATACTCTAGCATCTTGATCCGCCGCACCGGGTCCGTCTTTAGATTCTCCTGCCCTTTCCTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46738232..46739351 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 111583 RMVar_ID_111583 Human_SNP_ID_833145563 m1A Human chr19 - 8426693 8426693 8426693 AGCCACTTCTCCAGACAGCTCTTATGCACGGCACCCAGCGTGCCGGTGCAGCCACACGGGGACAG AGCCACTTCTCCAGACAGCTCTTATGCACGGCGCCCAGCGTGCCGGTGCAGCCACACGGGGACAG T C AC136469.1 Ensembl:ENSG00000268931 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8418766..8430833 32194978 MeRIP-seq:(Medium) rs1383667084 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111584 RMVar_ID_111584 Human_SNP_ID_833146329 m1A Human chr19 - 11419291 11419291 11419291 TTCCGCCTCACTCAGCGGCGCCACTGAGAGGGACGGGCGCCGGCCATGGAGCGCACAGCAGGCAA TTCCGCCTCACTCAGCGGCGCCACTGAGAGGGGCGGGCGCCGGCCATGGAGCGCACAGCAGGCAA T C RGL3 Ensembl:ENSG00000205517 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:11419181..11419299 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_18421270 Human_Splice_Rec_1960311,Human_Splice_Rec_1960347,Human_Splice_Rec_1960409,Human_Splice_Rec_1960451,Human_Splice_Rec_1960499,Human_Splice_Rec_1960521,Human_Splice_Rec_1960543,Human_Splice_Rec_1960551,Human_Splice_Rec_1960555 111585 RMVar_ID_111585 Human_SNP_ID_833150057 m1A Human chr19 + 1508024 1508024 1508024 AGTCACCGGCGTCACGAAACACGCGCTGCACGAAAAGGCACGAGTCGTTGGCGCCTCCGCAGCGG AGTCACCGGCGTCACGAAACACGCGCTGCACGCAAAGGCACGAGTCGTTGGCGCCTCCGCAGCGG A C PLK5 Ensembl:ENSG00000185988 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:1507981..1508133 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_Splice_Rec_1933199 111586 RMVar_ID_111586 Human_SNP_ID_833150384 m1A Human chr19 + 13149784 13149784 13149784 GGTCCCACTCGATGCTGCGCAGGCCATTCCGCAGCTCATTGGTCGTCCAGTCCAGCTCCTCGCGT GGTCCCACTCGATGCTGCGCAGGCCATTCCGCGGCTCATTGGTCGTCCAGTCCAGCTCCTCGCGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:13149726..13149978 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain 111587 RMVar_ID_111587 Human_SNP_ID_833150946 m1A Human chr19 - 39488617 39488617 39488617 CAACCTGCTCTAGCCGGCTTTGCCGCTGTTTGAAAGCCGCCAGCGGGTCATCCTCCAGGGCATAG CAACCTGCTCTAGCCGGCTTTGCCGCTGTTTGGAAGCCGCCAGCGGGTCATCCTCCAGGGCATAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39488566..39488670 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 111588 RMVar_ID_111588 Human_SNP_ID_833165937 m1A Human chr19 + 18437029 18437029 18437029 CCACCATGGGCAGCACCGCGCTGAAGGGTACGAACACCTCCTGGCCCTCGGCGTCCAGGCCCAGG CCACCATGGGCAGCACCGCGCTGAAGGGTACGGACACCTCCTGGCCCTCGGCGTCCAGGCCCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18436951..18437100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 111589 RMVar_ID_111589 Human_SNP_ID_833166537 m1A Human chr19 - 49498033 49498033 49498033 GATGGGCCACTGCGCTCACCTGAAGCAGGGGGACAGGTGTACAGACATGTTCTTGTGGCGCTTCT GATGGGCCACTGCGCTCACCTGAAGCAGGGGGGCAGGTGTACAGACATGTTCTTGTGGCGCTTCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:49497901..49498082;chr19:49497976..49498082 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 111590 RMVar_ID_111590 Human_SNP_ID_833169703 m1A Human chr19 - 12769977 12769977 12769977 GAGCTGCGGCGGCAGGTGCGGCAGCTGGAGGAACGCAACGCCGGCCACGCCGAGCGCACGCGACA GAGCTGCGGCGGCAGGTGCGGCAGCTGGAGGAGCGCAACGCCGGCCACGCCGAGCGCACGCGACA T C HOOK2 Ensembl:ENSG00000095066 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12769931..12770007 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_18996773,Human_RBP_ID_22977416,Human_RBP_ID_27816131 Human_Splice_Rec_1963353,Human_Splice_Rec_1963397 RMVar_hsa_circ_75656,RMVar_hsa_circ_192784,RMVar_hsa_circ_326967 111591 RMVar_ID_111591 Human_SNP_ID_833171631 m1A Human chr19 + 35157500 35157500 35157500 ATCATGGACATTCAGGTCCCGACACGAGCCCCAGGTGAGGAAAGGGACACATCTATCAAGATCCT ATCATGGACATTCAGGTCCCGACACGAGCCCCGGGTGAGGAAAGGGACACATCTATCAAGATCCT A G FXYD5 Ensembl:ENSG00000089327 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:35157476..35157525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 10 uterus Human_RBP_ID_770257,Human_RBP_ID_18728924,Human_RBP_ID_26815690 Human_Splice_Rec_1992612,Human_Splice_Rec_1992613,Human_Splice_Rec_1992620,Human_Splice_Rec_1992621,Human_Splice_Rec_1992634,Human_Splice_Rec_1992635,Human_Splice_Rec_1992650,Human_Splice_Rec_1992666,Human_Splice_Rec_1992667,Human_Splice_Rec_1992682,Human_Splice_Rec_1992683,Human_Splice_Rec_1992700,Human_Splice_Rec_1992701,Human_Splice_Rec_1992714,Human_Splice_Rec_1992715,Human_Splice_Rec_1992730,Human_Splice_Rec_1992731,Human_Splice_Rec_1992746,Human_Splice_Rec_1992747 RMVar_hsa_circ_77352,RMVar_hsa_circ_105676,RMVar_hsa_circ_194214,RMVar_hsa_circ_194215 111592 RMVar_ID_111592 Human_SNP_ID_833176187 m1A Human chr19 + 45076414 45076414 45076414 GGCCGGGCGAGCGAGCGGGCGGGCAGGCAGGCAGGCGGGCGGGCGGAGGACGCACGAGCGGAGGA GGCCGGGCGAGCGAGCGGGCGGGCAGGCAGGCGGGCGGGCGGGCGGAGGACGCACGAGCGGAGGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:45075826..45076463;chr19:45076222..45076453 26863196 MeRIP-seq:(Medium) rs1450502888 Functional Loss SNV ICGC 33..33 33 STAD 1 - 111593 RMVar_ID_111593 Human_SNP_ID_833178188 m1A Human chr19 - 15185278 15185278 15185278 CATGCAGCAGCGATGGAATGGGTTTCCACTGCACCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC CATGCAGCAGCGATGGAATGGGTTTCCACTGCTCCTGCCCGCCTGGTGTCCAGGGTGTGTACCTC T A NOTCH3 Ensembl:ENSG00000074181 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15184992..15185508 32194978 MeRIP-seq:(Medium) rs1442324683 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_514609 Human_Splice_Rec_1970453,Human_Splice_Rec_1970529 RMVar_hsa_circ_109200,RMVar_hsa_circ_111070,RMVar_hsa_circ_193094,RMVar_hsa_circ_108034,RMVar_hsa_circ_104390,RMVar_hsa_circ_193095,RMVar_hsa_circ_115610,RMVar_hsa_circ_193101,RMVar_hsa_circ_105182,RMVar_hsa_circ_193103,RMVar_hsa_circ_193106,RMVar_hsa_circ_266410,RMVar_hsa_circ_4986,RMVar_hsa_circ_94590,RMVar_hsa_circ_112719,RMVar_hsa_circ_193110,RMVar_hsa_circ_193111,RMVar_hsa_circ_324145,RMVar_hsa_circ_76833,RMVar_hsa_circ_4681,RMVar_hsa_circ_111564,RMVar_hsa_circ_193112,RMVar_hsa_circ_193113,RMVar_hsa_circ_38746,RMVar_hsa_circ_82699,RMVar_hsa_circ_193114,RMVar_hsa_circ_193115 111594 RMVar_ID_111594 Human_SNP_ID_833182082 m1A Human chr19 - 47780919 47780919 47780919 GTGCTCAAGTCTTTCTCCCCATCCCAAGACTCACGATGTCCAGGCGGCCGGGGAACTCATCTTCT GTGCTCAAGTCTTTCTCCCCATCCCAAGACTCGCGATGTCCAGGCGGCCGGGGAACTCATCTTCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:47779731..47780986 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111595 RMVar_ID_111595 Human_SNP_ID_833184914 m1A Human chr19 + 49487643 49487643 49487643 TTCCAAGCGGCTGCCGAAGATGGCGGAGGTGCAGGTATGGGCTCCGCGCGGGCCGGGGCGGCAAG TTCCAAGCGGCTGCCGAAGATGGCGGAGGTGCCGGTATGGGCTCCGCGCGGGCCGGGGCGGCAAG A C RPL13A Ensembl:ENSG00000142541 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49487631..49487758 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_240408,Human_RBP_ID_771810,Human_RBP_ID_826295,Human_RBP_ID_915165,Human_RBP_ID_4559811,Human_RBP_ID_13495419,Human_RBP_ID_18192402,Human_RBP_ID_18421672,Human_RBP_ID_27277017 Human_Splice_Rec_2030649,Human_Splice_Rec_2030661,Human_Splice_Rec_2030675,Human_Splice_Rec_2030683,Human_Splice_Rec_2030697,Human_Splice_Rec_2030701,Human_Splice_Rec_2030715,Human_Splice_Rec_2030727,Human_Splice_Rec_2030733,Human_Splice_Rec_2030747 Human_miRNA_ID_2751256 RMVar_hsa_circ_81809,RMVar_hsa_circ_121194,RMVar_hsa_circ_370369,RMVar_hsa_circ_117654,RMVar_hsa_circ_195849,RMVar_hsa_circ_195851,RMVar_hsa_circ_195852,RMVar_hsa_circ_195850 111596 RMVar_ID_111596 Human_SNP_ID_833190217 m1A Human chr19 - 48150202 48150202 48150202 ACCGTCTGAGCTCTCTCACCGCAGAAGCAGAGACCCCGACGGAAAGCGTTTCAGAGCCTGAGGTG ACCGTCTGAGCTCTCTCACCGCAGAAGCAGAGGCCCCGACGGAAAGCGTTTCAGAGCCTGAGGTG T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:48150151..48150225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_914964,Human_RBP_ID_18998328 Human_Splice_Rec_2025188,Human_Splice_Rec_2025238,Human_Splice_Rec_2025294,Human_Splice_Rec_2025344,Human_Splice_Rec_2025388,Human_Splice_Rec_2025440,Human_Splice_Rec_2025492,Human_Splice_Rec_2025572,Human_Splice_Rec_2025590,Human_Splice_Rec_2025598,Human_Splice_Rec_2025606,Human_Splice_Rec_2025616 RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_376509,RMVar_hsa_circ_119674,RMVar_hsa_circ_95771,RMVar_hsa_circ_103030,RMVar_hsa_circ_86212,RMVar_hsa_circ_4035,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,RMVar_hsa_circ_195644,RMVar_hsa_circ_195643,RMVar_hsa_circ_195640,RMVar_hsa_circ_195641,RMVar_hsa_circ_91105,RMVar_hsa_circ_195649,RMVar_hsa_circ_126783,RMVar_hsa_circ_195651,RMVar_hsa_circ_195652,RMVar_hsa_circ_3893,RMVar_hsa_circ_48843,RMVar_hsa_circ_34463,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_83444,RMVar_hsa_circ_195654,RMVar_hsa_circ_295820,RMVar_hsa_circ_304632,RMVar_hsa_circ_317913,RMVar_hsa_circ_62852,RMVar_hsa_circ_195655,RMVar_hsa_circ_195656,RMVar_hsa_circ_195657 111597 RMVar_ID_111597 Human_SNP_ID_833191187 m1A Human chr19 + 41265151 41265151 41265151 GAGGTTTTCCGTTTGGGTTGGGGAGGGTCTCGAAAATGGGGATCCTAGGGTACGGAGCTCCGTGG GAGGTTTTCCGTTTGGGTTGGGGAGGGTCTCGGAAATGGGGATCCTAGGGTACGGAGCTCCGTGG A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:41265105..41265350 26863196 MeRIP-seq:(Medium) rs117710350 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_3581265,Human_RBP_ID_5320406,Human_RBP_ID_6765730,Human_RBP_ID_8100664,Human_RBP_ID_8196508,Human_RBP_ID_9425339,Human_RBP_ID_17190832,Human_RBP_ID_18490715,Human_RBP_ID_18945484,Human_RBP_ID_21977982 Human_Splice_Rec_2010981 111598 RMVar_ID_111598 Human_SNP_ID_833191675 m1A Human chr19 + 11060125 11060125 11060125 AGGACCGGCTGAAGGGCGGCCGGCGGCGGCCGAGCCGAGGGTCCCGAGCCAAGCCGGTCGTGAGT AGGACCGGCTGAAGGGCGGCCGGCGGCGGCCGGGCCGAGGGTCCCGAGCCAAGCCGGTCGTGAGT A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11060101..11060125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 18 large intestine Human_RBP_ID_8839792,Human_RBP_ID_17935244,Human_RBP_ID_18412498,Human_RBP_ID_26335720,Human_RBP_ID_27815140 Human_Splice_Rec_1956930,Human_Splice_Rec_1956931,Human_Splice_Rec_1956996,Human_Splice_Rec_1956997,Human_Splice_Rec_1957066,Human_Splice_Rec_1957067,Human_Splice_Rec_1957134,Human_Splice_Rec_1957135,Human_Splice_Rec_1957200,Human_Splice_Rec_1957201,Human_Splice_Rec_1957264,Human_Splice_Rec_1957265,Human_Splice_Rec_1957332,Human_Splice_Rec_1957333,Human_Splice_Rec_1957396,Human_Splice_Rec_1957397,Human_Splice_Rec_1957462,Human_Splice_Rec_1957463,Human_Splice_Rec_1957530,Human_Splice_Rec_1957531,Human_Splice_Rec_1957600,Human_Splice_Rec_1957601,Human_Splice_Rec_1957674,Human_Splice_Rec_1957675,Human_Splice_Rec_1957740,Human_Splice_Rec_1957741,Human_Splice_Rec_1957806,Human_Splice_Rec_1957807,Human_Splice_Rec_1957874,Human_Splice_Rec_1957875,Human_Splice_Rec_1957940,Human_Splice_Rec_1957941,Human_Splice_Rec_1958004,Human_Splice_Rec_1958005,Human_Splice_Rec_1958072,Human_Splice_Rec_1958073,Human_Splice_Rec_1958178,Human_Splice_Rec_1958179,Human_Splice_Rec_1958234,Human_Splice_Rec_1958235,Human_Splice_Rec_1958284,Human_Splice_Rec_1958285,Human_Splice_Rec_1958336,Human_Splice_Rec_1958337,Human_Splice_Rec_1958388,Human_Splice_Rec_1958389,Human_Splice_Rec_1958438,Human_Splice_Rec_1958439,Human_Splice_Rec_1958492,Human_Splice_Rec_1958493,Human_Splice_Rec_1958570,Human_Splice_Rec_1958571,Human_Splice_Rec_1958656,Human_Splice_Rec_1958657,Human_Splice_Rec_1958706,Human_Splice_Rec_1958707,Human_Splice_Rec_1958756,Human_Splice_Rec_1958757,Human_Splice_Rec_1958804,Human_Splice_Rec_1958805,Human_Splice_Rec_1958868,Human_Splice_Rec_1958869,Human_Splice_Rec_1958908,Human_Splice_Rec_1958909,Human_Splice_Rec_1958942,Human_Splice_Rec_1958943,Human_Splice_Rec_1958988,Human_Splice_Rec_1958989,Human_Splice_Rec_1959040,Human_Splice_Rec_1959041,Human_Splice_Rec_1959074,Human_Splice_Rec_1959075,Human_Splice_Rec_1959094,Human_Splice_Rec_1959095,Human_Splice_Rec_1959110,Human_Splice_Rec_1959111,Human_Splice_Rec_1959124,Human_Splice_Rec_1959125,Human_Splice_Rec_1959140,Human_Splice_Rec_1959141,Human_Splice_Rec_1959150,Human_Splice_Rec_1959151 RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_192489,RMVar_hsa_circ_8398,RMVar_hsa_circ_192495,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_192494,RMVar_hsa_circ_277811,RMVar_hsa_circ_308346,RMVar_hsa_circ_192496,RMVar_hsa_circ_301128 111599 RMVar_ID_111599 Human_SNP_ID_833193545 m1A Human chr19 - 15238255 15238255 15238255 CCAGGGGATGCCTCAGGGCCTGGCCCTCCTGCATGCTATGCCCGGGGCAGGCCTGACGGGCAGCT CCAGGGGATGCCTCAGGGCCTGGCCCTCCTGCGTGCTATGCCCGGGGCAGGCCTGACGGGCAGCT T C BRD4 Ensembl:ENSG00000141867 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:15238205..15238290 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4506374,Human_RBP_ID_5320222,Human_RBP_ID_8839853,Human_RBP_ID_9293475,Human_RBP_ID_17271780,Human_RBP_ID_18192071,Human_RBP_ID_18470530,Human_RBP_ID_20432788,Human_RBP_ID_21977746,Human_RBP_ID_22719136,Human_RBP_ID_26472150,Human_RBP_ID_27269010 111600 RMVar_ID_111600 Human_SNP_ID_833196488 m1A Human chr19 - 46229776 46229776 46229776 CCTCCTTACCTACGATGCAGCCTCGGGGAGCCATGGCTCTGGGTGGTTGCAGTGGAGTGAGGAGG CCTCCTTACCTACGATGCAGCCTCGGGGAGCCTTGGCTCTGGGTGGTTGCAGTGGAGTGAGGAGG T A AC006262.3 Ensembl:ENSG00000269745 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46229759..46229833 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 111601 RMVar_ID_111601 Human_SNP_ID_833198841 m1A Human chr19 - 12922871 12922871 12922871 GTTCCCTCCCCCACAAGCCCAACGATGATCAAATATGGCATCAACAATATCCGGGAGCTGGTGGG GTTCCCTCCCCCACAAGCCCAACGATGATCAAGTATGGCATCAACAATATCCGGGAGCTGGTGGG T C FARSA Ensembl:ENSG00000179115 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:12922626..12922900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 3 bladder,urinary tract Human_RBP_ID_909396,Human_RBP_ID_1554836,Human_RBP_ID_3563337,Human_RBP_ID_17915352,Human_RBP_ID_25384472,Human_RBP_ID_26464630 Human_Splice_Rec_1964226,Human_Splice_Rec_1964252,Human_Splice_Rec_1964274,Human_Splice_Rec_1964298,Human_Splice_Rec_1964320 RMVar_hsa_circ_192819,RMVar_hsa_circ_77885 111602 RMVar_ID_111602 Human_SNP_ID_833199853 m1A Human chr19 + 2431631 2431631 2431631 CTCCCCATTCTCATTCTCACGCATCACCGAGGACTTCTTCACAGTCCTCATGGCCACTTCCTGTG CTCCCCATTCTCATTCTCACGCATCACCGAGGGCTTCTTCACAGTCCTCATGGCCACTTCCTGTG A G lnc-GADD45B-1 RNACentral:URS00008B2542 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2431543..2431692 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 111603 RMVar_ID_111603 Human_SNP_ID_833202263 m1A Human chr19 - 18745916 18745916 18745916 TTTGTCCACTGACAGGGGCCGGCGGTGTGGGGAGCCGAGCCGGCCACGCTCCCGGTACACCCTGT TTTGTCCACTGACAGGGGCCGGCGGTGTGGGGGGCCGAGCCGGCCACGCTCCCGGTACACCCTGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:18745868..18747060 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 9 ovary 111604 RMVar_ID_111604 Human_SNP_ID_833203428 m1A Human chr19 + 55685511 55685511 55685511 GACGCTGAAGGACTTCCAGTACGTGGACCGCGACGGCAAGGACCAGGGCGTGAACGTGCGTGAGA GACGCTGAAGGACTTCCAGTACGTGGACCGCGGCGGCAAGGACCAGGGCGTGAACGTGCGTGAGA A G EPN1 Ensembl:ENSG00000063245 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55685359..55691981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_527285,Human_RBP_ID_1571344,Human_RBP_ID_1891914,Human_RBP_ID_6784500,Human_RBP_ID_8837281,Human_RBP_ID_18192516 RMVar_hsa_circ_9292,RMVar_hsa_circ_89787,RMVar_hsa_circ_57284,RMVar_hsa_circ_375242,RMVar_hsa_circ_196363,RMVar_hsa_circ_332992,RMVar_hsa_circ_196364,RMVar_hsa_circ_196365,RMVar_hsa_circ_331802 111605 RMVar_ID_111605 Human_SNP_ID_833206365 m1A Human chr19 - 863295 863295 863295 CAATAAAGACCAACCAGATGCAGGAGTGGATGACTTCATTGCTCGGGACTTTGTTGCTTGGGTGA CAATAAAGACCAACCAGATGCAGGAGTGGATGGCTTCATTGCTCGGGACTTTGTTGCTTGGGTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:863245..863501 26863196 MeRIP-seq:(Medium) rs943735680 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_2572684,Human_RBP_ID_3579165,Human_RBP_ID_5500409,Human_RBP_ID_13537976 111606 RMVar_ID_111606 Human_SNP_ID_833211292 m1A Human chr19 + 47152968 47152968 47152968 AGTTGACCAGATCTGTCACAAAAATAGCATCAAGTTCTTTACAGGAGATGTTTTTGGCTACCATG AGTTGACCAGATCTGTCACAAAAATAGCATCACGTTCTTTACAGGAGATGTTTTTGGCTACCATG A C SAE1 Ensembl:ENSG00000142230 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47152857..47153000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 colon adenocarcinoma,UCEC,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_1017312,Human_RBP_ID_1568927,Human_RBP_ID_1890501,Human_RBP_ID_17501057,Human_RBP_ID_18736516,Human_RBP_ID_23802627 Human_Splice_Rec_2023402,Human_Splice_Rec_2023403,Human_Splice_Rec_2023414,Human_Splice_Rec_2023420,Human_Splice_Rec_2023421,Human_Splice_Rec_2023428,Human_Splice_Rec_2023429,Human_Splice_Rec_2023442,Human_Splice_Rec_2023443,Human_Splice_Rec_2023452,Human_Splice_Rec_2023453,Human_Splice_Rec_2023480,Human_Splice_Rec_2023481,Human_Splice_Rec_2023496,Human_Splice_Rec_2023502,Human_Splice_Rec_2023503,Human_Splice_Rec_2023520,Human_Splice_Rec_2023521,Human_Splice_Rec_2023536,Human_Splice_Rec_2023537,Human_Splice_Rec_2023554,Human_Splice_Rec_2023555,Human_Splice_Rec_2023568,Human_Splice_Rec_2023569 RMVar_hsa_circ_9265,RMVar_hsa_circ_195557,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_338592,RMVar_hsa_circ_272792,RMVar_hsa_circ_195558,RMVar_hsa_circ_317076,RMVar_hsa_circ_299077,RMVar_hsa_circ_195560,RMVar_hsa_circ_195561,RMVar_hsa_circ_363271,RMVar_hsa_circ_356999 111607 RMVar_ID_111607 Human_SNP_ID_833212582 m1A Human chr19 - 6750032 6750032 6750032 CATACTTCTGCACTTCCAATTTCAGCCGTTCAATGTTGCTCAGGGTTTCAGCGATCTGGGGCTCC CATACTTCTGCACTTCCAATTTCAGCCGTTCAGTGTTGCTCAGGGTTTCAGCGATCTGGGGCTCC T C AC008760.1 Ensembl:ENSG00000269680 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:6749982..6750101 26863196 MeRIP-seq:(Medium) rs544311636 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 6 kidney 111608 RMVar_ID_111608 Human_SNP_ID_833216753 m1A Human chr19 - 45052798 45052798 45052798 TCGGTCAATCATGTTGTTGGTGTCCCCCTGCCAGGGCATCCTGAAGTGGGAGGGGAGCAAGAAAG TCGGTCAATCATGTTGTTGGTGTCCCCCTGCCGGGGCATCCTGAAGTGGGAGGGGAGCAAGAAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45040746..45053090 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111609 RMVar_ID_111609 Human_SNP_ID_833217676 m1A Human chr19 + 8455340 8455340 8455340 TTGTGTGGAATTGTAAACCTGGCAAATCAAATAATTATCTTTCACATTGTGCTGACATATAAACC TTGTGTGGAATTGTAAACCTGGCAAATCAAATTATTATCTTTCACATTGTGCTGACATATAAACC A T HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:8455337..8455550 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_9090561 111610 RMVar_ID_111610 Human_SNP_ID_833219462 m1A Human chr19 - 48714028 48714028 48714028 TCTTGGCTGCTCTAGGTCAAGCCCAGCGCAGCATCTCACAGGCCACCTCTTCCACGTGCCGCGGA TCTTGGCTGCTCTAGGTCAAGCCCAGCGCAGCGTCTCACAGGCCACCTCTTCCACGTGCCGCGGA T C MAMSTR Ensembl:ENSG00000176909 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48713977..48714060 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_Splice_Rec_2027302,Human_Splice_Rec_2027316,Human_Splice_Rec_2027328 RMVar_hsa_circ_101482,RMVar_hsa_circ_119554,RMVar_hsa_circ_195711,RMVar_hsa_circ_88904,RMVar_hsa_circ_195710,RMVar_hsa_circ_195712 111611 RMVar_ID_111611 Human_SNP_ID_833220755 m1A Human chr19 + 1105767 1105767 1105767 CGTGAACGGGGACGACGCCCACCCGCTGTGGAAGTGGATGAAGATCCAACCCAAGGGCAAGGGCA CGTGAACGGGGACGACGCCCACCCGCTGTGGAGGTGGATGAAGATCCAACCCAAGGGCAAGGGCA A G GPX4 Ensembl:ENSG00000167468 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1105717..1105828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 6 oesophagus Human_RBP_ID_512678,Human_RBP_ID_5115921,Human_RBP_ID_9084333,Human_RBP_ID_17655734,Human_RBP_ID_23210769,Human_RBP_ID_23781446,Human_RBP_ID_26814788 Human_Splice_Rec_1930879,Human_Splice_Rec_1930891,Human_Splice_Rec_1930903,Human_Splice_Rec_1930913,Human_Splice_Rec_1930925,Human_Splice_Rec_1930935,Human_Splice_Rec_1930953,Human_Splice_Rec_1930967,Human_Splice_Rec_1930985 RMVar_hsa_circ_82082,RMVar_hsa_circ_88406,RMVar_hsa_circ_87071,RMVar_hsa_circ_190989,RMVar_hsa_circ_370246,RMVar_hsa_circ_190991,RMVar_hsa_circ_81395,RMVar_hsa_circ_190992,RMVar_hsa_circ_190990,RMVar_hsa_circ_190993 111612 RMVar_ID_111612 Human_SNP_ID_833229636 m1A Human chr19 - 1091842 1091842 1091842 TGTACTGCCAGCGCATGCAGGAGGAGAACATCACACGGGCTCTCATCGTGGTGCAGCAGGGCATG TGTACTGCCAGCGCATGCAGGAGGAGAACATCTCACGGGCTCTCATCGTGGTGCAGCAGGGCATG T A POLR2E Ensembl:ENSG00000099817 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1091753..1091878 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung Human_RBP_ID_770422,Human_RBP_ID_13361786,Human_RBP_ID_17266585,Human_RBP_ID_22228892,Human_RBP_ID_22448102,Human_RBP_ID_26464142,Human_RBP_ID_26814783 Human_Splice_Rec_1930726,Human_Splice_Rec_1930727,Human_Splice_Rec_1930740,Human_Splice_Rec_1930741,Human_Splice_Rec_1930752,Human_Splice_Rec_1930753,Human_Splice_Rec_1930768,Human_Splice_Rec_1930769,Human_Splice_Rec_1930782,Human_Splice_Rec_1930783,Human_Splice_Rec_1930794,Human_Splice_Rec_1930795,Human_Splice_Rec_1930808,Human_Splice_Rec_1930809,Human_Splice_Rec_1930820,Human_Splice_Rec_1930821,Human_Splice_Rec_1930834,Human_Splice_Rec_1930835,Human_Splice_Rec_1930846,Human_Splice_Rec_1930847,Human_Splice_Rec_1930860,Human_Splice_Rec_1930861,Human_Splice_Rec_1930870 Human_miRNA_ID_1093868 RMVar_hsa_circ_81258,RMVar_hsa_circ_84576,RMVar_hsa_circ_104627,RMVar_hsa_circ_29423,RMVar_hsa_circ_190977,RMVar_hsa_circ_125341,RMVar_hsa_circ_375778,RMVar_hsa_circ_190981,RMVar_hsa_circ_190982,RMVar_hsa_circ_11738,RMVar_hsa_circ_109467,RMVar_hsa_circ_126742,RMVar_hsa_circ_344438,RMVar_hsa_circ_190984,RMVar_hsa_circ_272878,RMVar_hsa_circ_190986,RMVar_hsa_circ_92578,RMVar_hsa_circ_190987,RMVar_hsa_circ_190985,RMVar_hsa_circ_190988 111613 RMVar_ID_111613 Human_SNP_ID_833229842 m1A Human chr19 + 1840637 1840637 1840637 CCAGTAATCCTGTGTTTGGAAACACTCGCCCCACCCCCCTGCAACTCTGAGTGACACCCGGGCCC CCAGTAATCCTGTGTTTGGAAACACTCGCCCCCCCCCCCTGCAACTCTGAGTGACACCCGGGCCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1840590..1840756 26863196 MeRIP-seq:(Medium) rs971410943 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111614 RMVar_ID_111614 Human_SNP_ID_833233407 m1A Human chr19 + 17516246 17516246 17516246 GATCACCATTAACCCCGAGCTGCCTGTGGAGGAGGCGGCTGAGGACTACGCCAAGAAGCTGAGAC GATCACCATTAACCCCGAGCTGCCTGTGGAGGCGGCGGCTGAGGACTACGCCAAGAAGCTGAGAC A C PGLS Ensembl:ENSG00000130313 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17516134..17516300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_240233,Human_RBP_ID_515800,Human_RBP_ID_771603,Human_RBP_ID_17916928,Human_RBP_ID_18192085,Human_RBP_ID_19089654 Human_Splice_Rec_1977146,Human_Splice_Rec_1977147,Human_Splice_Rec_1977156,Human_Splice_Rec_1977157,Human_Splice_Rec_1977166,Human_Splice_Rec_1977167,Human_Splice_Rec_1977172,Human_Splice_Rec_1977173,Human_Splice_Rec_1977177 Human_miRNA_ID_3010997 RMVar_hsa_circ_124206,RMVar_hsa_circ_193325,RMVar_hsa_circ_80786,RMVar_hsa_circ_295626,RMVar_hsa_circ_367593,RMVar_hsa_circ_274157,RMVar_hsa_circ_193327,RMVar_hsa_circ_193329,RMVar_hsa_circ_92242,RMVar_hsa_circ_193328,RMVar_hsa_circ_193326 111615 RMVar_ID_111615 Human_SNP_ID_833234069 m1A Human chr19 + 35267732 35267732 35267732 ACTCGCAGGCGTCCCGAGAGCGCAGGCTCAAGAAGGTGAGGGCCGCCCTCCCTGGCGTCCAGACC ACTCGCAGGCGTCCCGAGAGCGCAGGCTCAAGCAGGTGAGGGCCGCCCTCCCTGGCGTCCAGACC A C LSR Ensembl:ENSG00000105699 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35267728..35267850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 10 large intestine Human_Splice_Rec_1992799,Human_Splice_Rec_1992817,Human_Splice_Rec_1992835,Human_Splice_Rec_1992851,Human_Splice_Rec_1992867,Human_Splice_Rec_1992883,Human_Splice_Rec_1992895,Human_Splice_Rec_1992913 RMVar_hsa_circ_113935,RMVar_hsa_circ_125886,RMVar_hsa_circ_194221,RMVar_hsa_circ_194222 111616 RMVar_ID_111616 Human_SNP_ID_833235166 m1A Human chr19 - 39507393 39507385 39507393 GCAAAAGGTAGCGCTGAGGGTCCCCGGGCCTGAGGCCCGGCGGGGCCGCGGGCAAGGCGCTTGCG GCAAAAGGTAGCGCTGAGGGTCCCCGGGCCTG________CGGGGCCGCGGGCAAGGCGCTTGCG GCCGGGCCT G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:39507209..39507600 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..40 33 PAAD 1 - 111617 RMVar_ID_111617 Human_SNP_ID_833235765 m1A Human chr19 - 1599553 1599553 1599553 CTGACCATCCCCTCTCCTCTCGCAGGGTCCCGACGGCCTACACATGGGGCGCTGTGGGCGCCGTG CTGACCATCCCCTCTCCTCTCGCAGGGTCCCGGCGGCCTACACATGGGGCGCTGTGGGCGCCGTG T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:1585126..1605475 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_514965,Human_RBP_ID_914861,Human_RBP_ID_4557013,Human_RBP_ID_5319821,Human_RBP_ID_5469517,Human_RBP_ID_8942117,Human_RBP_ID_17655286,Human_RBP_ID_22446292,Human_RBP_ID_22661540,Human_RBP_ID_26814842,Human_RBP_ID_27269310 Human_Splice_Rec_1933466,Human_Splice_Rec_1933478,Human_Splice_Rec_1933482,Human_Splice_Rec_1933486,Human_Splice_Rec_1933492,Human_Splice_Rec_1933496 Human_miRNA_ID_2772773 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 111618 RMVar_ID_111618 Human_SNP_ID_833239205 m1A Human chr19 + 16871301 16871301 16871301 CATGGTGCGGAGCCTGCTGGAGGGCAGCATCGACCCCACGCAGTACGAGGACACCCTACGCGAGA CATGGTGCGGAGCCTGCTGGAGGGCAGCATCGGCCCCACGCAGTACGAGGACACCCTACGCGAGA A G SIN3B Ensembl:ENSG00000127511 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16869701..16871504 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_5526889,Human_RBP_ID_9382262,Human_RBP_ID_18994558,Human_RBP_ID_22977435,Human_RBP_ID_27816276 Human_Splice_Rec_1974762,Human_Splice_Rec_1974763,Human_Splice_Rec_1974814,Human_Splice_Rec_1974815,Human_Splice_Rec_1974848,Human_Splice_Rec_1974849,Human_Splice_Rec_1974864,Human_Splice_Rec_1974865,Human_Splice_Rec_1974868 RMVar_hsa_circ_77626,RMVar_hsa_circ_373268,RMVar_hsa_circ_193214,RMVar_hsa_circ_193218,RMVar_hsa_circ_48791,RMVar_hsa_circ_269527,RMVar_hsa_circ_307803,RMVar_hsa_circ_193223 111619 RMVar_ID_111619 Human_SNP_ID_833239436 m1A Human chr19 - 648142 648142 648142 CCTCCTCCAGCTCGCCCAGCAACGAGAACGCCACAAGCAACTCGTGAGCCCACGTCGGCCGTCGG CCTCCTCCAGCTCGCCCAGCAACGAGAACGCCGCAAGCAACTCGTGAGCCCACGTCGGCCGTCGG T C RNF126 Ensembl:ENSG00000070423 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:648117..648282 26863196 MeRIP-seq:(Medium) rs1391849051 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_26470882,Human_RBP_ID_27472576 111620 RMVar_ID_111620 Human_SNP_ID_833242725 m1A Human chr19 + 9828338 9828338 9828338 CCCACCCCCCGCTTTGTGTAGCTCCAGCTAGGATGATCGAGGTTGTTTGCAACGACCGTCTGGGG CCCACCCCCCGCTTTGTGTAGCTCCAGCTAGGGTGATCGAGGTTGTTTGCAACGACCGTCTGGGG A G UBL5 Ensembl:ENSG00000198258 Protein coding start codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:9827926..9828352 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_240803,Human_RBP_ID_530235,Human_RBP_ID_909295,Human_RBP_ID_4557201,Human_RBP_ID_5116043,Human_RBP_ID_5144997,Human_RBP_ID_5320135,Human_RBP_ID_9328564,Human_RBP_ID_9380315,Human_RBP_ID_17655915,Human_RBP_ID_22448342 Human_Splice_Rec_1952566,Human_Splice_Rec_1952567,Human_Splice_Rec_1952574,Human_Splice_Rec_1952575,Human_Splice_Rec_1952582,Human_Splice_Rec_1952583,Human_Splice_Rec_1952590,Human_Splice_Rec_1952591,Human_Splice_Rec_1952594,Human_Splice_Rec_1952598,Human_Splice_Rec_1952600,Human_Splice_Rec_1952604,Human_Splice_Rec_1952605 RMVar_hsa_circ_109466,RMVar_hsa_circ_119094,RMVar_hsa_circ_90646,RMVar_hsa_circ_192244,RMVar_hsa_circ_192245,RMVar_hsa_circ_267797,RMVar_hsa_circ_192247,RMVar_hsa_circ_100648,RMVar_hsa_circ_192246 111621 RMVar_ID_111621 Human_SNP_ID_833242787 m1A Human chr19 - 851482 851482 851482 GCCCCGTGATACCGGCCACATGCAGCTGTGTCACCTGCCTCAGTTTACCCAGGGCCCTGTGATAC GCCCCGTGATACCGGCCACATGCAGCTGTGTCGCCTGCCTCAGTTTACCCAGGGCCCTGTGATAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:851465..851536 26863196 MeRIP-seq:(Medium) rs1373463131 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 111622 RMVar_ID_111622 Human_SNP_ID_833244293 m1A Human chr19 + 4402799 4402799 4402799 TGGAGGAGCTGGAGTGCGGGGCGCCCGGCGCCAGGGGAGCCGCCACAGGTCGGTTCGGGCCCGCG TGGAGGAGCTGGAGTGCGGGGCGCCCGGCGCCGGGGGAGCCGCCACAGGTCGGTTCGGGCCCGCG A G CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:4402626..4409015;chr19:4402626..4402872;chr19:4402626..4402890 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_771974,Human_RBP_ID_914415,Human_RBP_ID_3954205,Human_RBP_ID_4557105,Human_RBP_ID_5145612,Human_RBP_ID_5321208,Human_RBP_ID_5372869,Human_RBP_ID_5526773,Human_RBP_ID_8838933,Human_RBP_ID_8942164,Human_RBP_ID_18420834,Human_RBP_ID_18470402,Human_RBP_ID_22977985,Human_RBP_ID_24552769,Human_RBP_ID_26335206 Human_Splice_Rec_1940011,Human_Splice_Rec_1940039,Human_Splice_Rec_1940043 RMVar_hsa_circ_117327,RMVar_hsa_circ_191530 111623 RMVar_ID_111623 Human_SNP_ID_833249273 m1A Human chr19 + 19516303 19516303 19516303 TCCGCCGGGGGGCTATGGGCCCATCGACTACAAACGGAACTTGCCGCGTCGAGGACTGTCGGGTC TCCGCCGGGGGGCTATGGGCCCATCGACTACACACGGAACTTGCCGCGTCGAGGACTGTCGGGTC A C NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding CDS,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_138703,Human_RBP_ID_240752,Human_RBP_ID_1556827,Human_RBP_ID_3564946,Human_RBP_ID_4512358,Human_RBP_ID_5116830,Human_RBP_ID_9085183,Human_RBP_ID_9328860,Human_RBP_ID_9382349,Human_RBP_ID_13404629,Human_RBP_ID_22447620,Human_RBP_ID_23114768,Human_RBP_ID_23787743,Human_RBP_ID_26336088,Human_RBP_ID_27815333 Human_Splice_Rec_1983479,Human_Splice_Rec_1983487,Human_Splice_Rec_1983495,Human_Splice_Rec_1983503,Human_Splice_Rec_1983505,Human_Splice_Rec_1983511,Human_Splice_Rec_1983515,Human_Splice_Rec_1983523,Human_Splice_Rec_1983535 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 111624 RMVar_ID_111624 Human_SNP_ID_833249813 m1A Human chr19 - 39356901 39356901 39356901 ACCAGCCAGCGAGGATGCCCACCTGGTCTCGGAACATCATGGTGCCGGGCCTGGGGCCAGGGTCG ACCAGCCAGCGAGGATGCCCACCTGGTCTCGGGACATCATGGTGCCGGGCCTGGGGCCAGGGTCG T C lnc-LRFN1-2 RNACentral:URS00008BA9A0 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39356852..39356917 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 111625 RMVar_ID_111625 Human_SNP_ID_833251171 m1A Human chr19 + 49867157 49867143 49867157 TCCGAGGGCAGGAAGATGGGGGGCGCTCCCCCAGGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC TCCGAGGGCAGGAAGATGG______________GGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC GGGGGCGCTCCCCCA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49867112..49867250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 20..33 33 MELA 1 - 111626 RMVar_ID_111626 Human_SNP_ID_833253717 m1A Human chr19 - 39406912 39406912 39406912 TGCGGCGGGGACTCACCTCGTAGATGGCAGTCAGATCCATGGTGTAACGGTTGGCCATGAGGGGT TGCGGCGGGGACTCACCTCGTAGATGGCAGTCTGATCCATGGTGTAACGGTTGGCCATGAGGGGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:39406861..39407844 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 111627 RMVar_ID_111627 Human_SNP_ID_833255877 m1A Human chr19 - 3535064 3535062 3535064 ATGTGGTTCTCGCCCTTTGGGAAGGGAGACAGAGCCCCTGCTGCTGAGGGTCCCCGACCACGTGC ATGTGGTTCTCGCCCTTTGGGAAGGGAGACAG__CCCCTGCTGCTGAGGGTCCCCGACCACGTGC GCT G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3535051..3535075 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 PBCA 1 - 111628 RMVar_ID_111628 Human_SNP_ID_833259180 m1A Human chr19 + 40780477 40780477 40780477 GTGGGAAGACTGTGAAGCTACAGATTTGGGACACGGCTGGCCAGGAGCGGTTTCGGTAGGTGGGC GTGGGAAGACTGTGAAGCTACAGATTTGGGACCCGGCTGGCCAGGAGCGGTTTCGGTAGGTGGGC A C RAB4B,RAB4B-EGLN2,MIA-RAB4B Ensembl:ENSG00000167578,Ensembl:ENSG00000171570,Ensembl:ENSG00000268975 Protein coding,Protein coding,Protein coding CDS,intron,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40780427..40780629 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_17925669,Human_RBP_ID_19090201 Human_Splice_Rec_2010044,Human_Splice_Rec_2010045,Human_Splice_Rec_2010058,Human_Splice_Rec_2010059,Human_Splice_Rec_2010072,Human_Splice_Rec_2010073,Human_Splice_Rec_2010086,Human_Splice_Rec_2010087,Human_Splice_Rec_2010093,Human_Splice_Rec_2010100,Human_Splice_Rec_2010101,Human_Splice_Rec_2010112,Human_Splice_Rec_2010113,Human_Splice_Rec_2010120,Human_Splice_Rec_2010121,Human_Splice_Rec_2010144,Human_Splice_Rec_2010145,Human_Splice_Rec_2010163 Human_miRNA_ID_2398540 RMVar_hsa_circ_194931,RMVar_hsa_circ_325843,RMVar_hsa_circ_324458,RMVar_hsa_circ_194930 111629 RMVar_ID_111629 Human_SNP_ID_833265097 m1A Human chr19 + 34227830 34227830 34227830 GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTTTTTCCTCCTTTCTTTTGGGG A G LSM14A Ensembl:ENSG00000257103 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs74404860 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LUSC 4 prostate Human_RBP_ID_519476,Human_RBP_ID_3568106,Human_RBP_ID_4519079,Human_RBP_ID_5292781,Human_RBP_ID_5650079,Human_RBP_ID_6743499,Human_RBP_ID_17267881,Human_RBP_ID_23792533,Human_RBP_ID_26652464,Human_RBP_ID_27839838 111630 RMVar_ID_111630 Human_SNP_ID_833266020 m1A Human chr19 + 10559907 10559907 10559907 GAAACAGCTCCCCTTCGTCTGAGGAGTCGTCCACAGCCAGCTGGACTGGGGGACCGTGGACCCTG GAAACAGCTCCCCTTCGTCTGAGGAGTCGTCCTCAGCCAGCTGGACTGGGGGACCGTGGACCCTG A T lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10559858..10561823 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 111631 RMVar_ID_111631 Human_SNP_ID_833266550 m1A Human chr19 + 10293176 10293176 10293176 GGCCTGCTGGGTCCAGTCACTCGGGCGCTCTCAGGCACTTACCGCTGCAAGGCGGCCAATGATCA GGCCTGCTGGGTCCAGTCACTCGGGCGCTCTCGGGCACTTACCGCTGCAAGGCGGCCAATGATCA A G ICAM5 Ensembl:ENSG00000105376 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10293126..10293225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_Splice_Rec_1954057,Human_Splice_Rec_1954077 111632 RMVar_ID_111632 Human_SNP_ID_833266961 m1A Human chr19 + 291347 291347 291347 CGAAGACCCACCTCCGCTGCATGGTCCCCGCGACCCCCGACGCCGGTCCCAGCGCGTCCCGTCGC CGAAGACCCACCTCCGCTGCATGGTCCCCGCGGCCCCCGACGCCGGTCCCAGCGCGTCCCGTCGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr19:291210..291461;chr19:291232..291358 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver 111633 RMVar_ID_111633 Human_SNP_ID_833269467 m1A Human chr19 + 19133200 19133200 19133200 GGCCCGAAGCTCCTCCTCAGACGGGTGCTTGTATCGGAACAAACTGAGAGCAAGGACGGGCAGTC GGCCCGAAGCTCCTCCTCAGACGGGTGCTTGTCTCGGAACAAACTGAGAGCAAGGACGGGCAGTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:19133151..19133225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111634 RMVar_ID_111634 Human_SNP_ID_833276196 m1A Human chr19 - 48874728 48874728 48874728 CACTCGGAAGGGGCAGGGCTCAGCTTCTCCCCAGTCCTCAGCAGCTTCCTCTTCCTCTGTCTCTT CACTCGGAAGGGGCAGGGCTCAGCTTCTCCCCTGTCCTCAGCAGCTTCCTCTTCCTCTGTCTCTT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:48874679..48874838 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 111635 RMVar_ID_111635 Human_SNP_ID_833277428 m1A Human chr19 - 45056536 45056536 45056536 TCCTCAACCCCCTGCACCCCAGACCCCGACTCACTTCTTCTTCTCATCTTCGCTGGGTCTCTGGA TCCTCAACCCCCTGCACCCCAGACCCCGACTCTCTTCTTCTTCTCATCTTCGCTGGGTCTCTGGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45056507..45056586 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 111636 RMVar_ID_111636 Human_SNP_ID_833282222 m1A Human chr19 - 1241897 1241897 1241897 CGGCGGCCTCGGCATAGGCACGGGCGTGGCGGACGAGGCGGCCAAGTCCCGGGCGGCGGAGCAGC CGGCGGCCTCGGCATAGGCACGGGCGTGGCGGCCGAGGCGGCCAAGTCCCGGGCGGCGGAGCAGC T G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr19:1241751..1242000 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine RMVar_hsa_circ_191022 111637 RMVar_ID_111637 Human_SNP_ID_833292019 m1A Human chr19 - 1108844 1108844 1108844 CGTGTGGGGCCGCATCGCCGCCGTCATGGCCGACGTCAGCAGCAGCAGCTACCTGCAGATCGTGC CGTGTGGGGCCGCATCGCCGCCGTCATGGCCGGCGTCAGCAGCAGCAGCTACCTGCAGATCGTGC T C SBNO2 Ensembl:ENSG00000064932 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:1108726..1108912 26863196 MeRIP-seq:(Medium) rs1327000840 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_9293108,Human_RBP_ID_18191550 Human_Splice_Rec_1931045,Human_Splice_Rec_1931107,Human_Splice_Rec_1931169,Human_Splice_Rec_1931181 RMVar_hsa_circ_31583,RMVar_hsa_circ_97372,RMVar_hsa_circ_121696,RMVar_hsa_circ_116073,RMVar_hsa_circ_121503,RMVar_hsa_circ_190996,RMVar_hsa_circ_190998,RMVar_hsa_circ_80337,RMVar_hsa_circ_190997,RMVar_hsa_circ_190995,RMVar_hsa_circ_265145,RMVar_hsa_circ_110593,RMVar_hsa_circ_119630,RMVar_hsa_circ_104909,RMVar_hsa_circ_190999,RMVar_hsa_circ_191001,RMVar_hsa_circ_191002,RMVar_hsa_circ_191000 111638 RMVar_ID_111638 Human_SNP_ID_833293760 m1A Human chr19 + 45040276 45040276 45040276 AGCTTCGAGGCATGATGGTCGACTACAAGAAGAGGGCGGAGCGGAGACGGGAGTATTATGAAAAG AGCTTCGAGGCATGATGGTCGACTACAAGAAGGGGGCGGAGCGGAGACGGGAGTATTATGAAAAG A G CLASRP Ensembl:ENSG00000104859 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45040176..45040325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_52989,Human_RBP_ID_5585769,Human_RBP_ID_6773065,Human_RBP_ID_9381103,Human_RBP_ID_18441617,Human_RBP_ID_18998062,Human_RBP_ID_22977768,Human_RBP_ID_25424557,Human_RBP_ID_26336380,Human_RBP_ID_27816499 Human_Splice_Rec_2018282,Human_Splice_Rec_2018283,Human_Splice_Rec_2018322,Human_Splice_Rec_2018323,Human_Splice_Rec_2018360,Human_Splice_Rec_2018361,Human_Splice_Rec_2018366,Human_Splice_Rec_2018367,Human_Splice_Rec_2018376,Human_Splice_Rec_2018377,Human_Splice_Rec_2018416,Human_Splice_Rec_2018419,Human_Splice_Rec_2018423,Human_Splice_Rec_2018459 RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 111639 RMVar_ID_111639 Human_SNP_ID_833295203 m1A Human chr19 + 1106691 1106691 1106691 GCTGGTGGGGCAGACCCGAAAATCCAGCGTGCACCCCGCCGGAGGAAGGTCCCATGGCCTGCTGG GCTGGTGGGGCAGACCCGAAAATCCAGCGTGCGCCCCGCCGGAGGAAGGTCCCATGGCCTGCTGG A G GPX4 Ensembl:ENSG00000167468 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1106642..1106742 32194978 MeRIP-seq:(Medium) rs948854873 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_512692,Human_RBP_ID_4561369,Human_RBP_ID_5421135,Human_RBP_ID_5498873,Human_RBP_ID_17914562,Human_RBP_ID_18208582,Human_RBP_ID_18721909,Human_RBP_ID_22592812,Human_RBP_ID_23781448,Human_RBP_ID_24374740,Human_RBP_ID_26464223,Human_RBP_ID_26982078,Human_RBP_ID_27267301,Human_RBP_ID_27463033 Human_miRNA_ID_2147283,Human_miRNA_ID_2988710,Human_miRNA_ID_3022409 RMVar_hsa_circ_82082,RMVar_hsa_circ_88406,RMVar_hsa_circ_190992,RMVar_hsa_circ_190993 111640 RMVar_ID_111640 Human_SNP_ID_833296040 m1A Human chr19 - 4325519 4325519 4325519 CATCAGGTCCTGCACCCTGCACAGGTGGCCCCAAGCCGCTGTCACCTGCGTCTAGCCAGGACAAG CATCAGGTCCTGCACCCTGCACAGGTGGCCCCTAGCCGCTGTCACCTGCGTCTAGCCAGGACAAG T A STAP2 Ensembl:ENSG00000178078 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:4325238..4325523 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_Splice_Rec_1939650,Human_Splice_Rec_1939682,Human_Splice_Rec_1939706,Human_Splice_Rec_1939734,Human_Splice_Rec_1939748,Human_Splice_Rec_1939762,Human_Splice_Rec_1939772,Human_Splice_Rec_1939788 Human_miRNA_ID_2878116 RMVar_hsa_circ_100802,RMVar_hsa_circ_191515 111641 RMVar_ID_111641 Human_SNP_ID_833301843 m1A Human chr19 + 3980977 3980977 3980977 GCGTCTCCGGCAGGCAGCCAGCGGCGCATCACAGCCTGCGGGGGCAGAGAGCGGTGCATGAGACA GCGTCTCCGGCAGGCAGCCAGCGGCGCATCACGGCCTGCGGGGGCAGAGAGCGGTGCATGAGACA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:3980699..3981045;chr19:3980825..3981010;chr19:3980821..3981012 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - 111642 RMVar_ID_111642 Human_SNP_ID_833305584 m1A Human chr19 + 892684 892655 892685 TCCCTCTCCAGGCCCCGCACCGATAACCCCGCAGTCTCCAGGCCCTGCCTCTACAGCCCCCCAGT TCCC______________________________TCTCCAGGCCCTGCCTCTACAGCCCCCCAGT CTCTCCAGGCCCCGCACCGATAACCCCGCAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:892653..892965 26863196 MeRIP-seq:(Medium) rs72298146 Functional Loss DEL ICGC 5..34 33 PAAD 3 - 111643 RMVar_ID_111643 Human_SNP_ID_833306169 m1A Human chr19 - 35745982 35745982 35745982 GGGACCCTAGCGATCTGCCTTACCCAGGTAGTACTTCCGGCACAGGTTCAATTTCTCCTCATTGG GGGACCCTAGCGATCTGCCTTACCCAGGTAGTGCTTCCGGCACAGGTTCAATTTCTCCTCATTGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:35745895..35746423 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 111644 RMVar_ID_111644 Human_SNP_ID_833307865 m1A Human chr19 - 47681080 47681080 47681080 GGGGCTGCTGCGCCTGCGGCTGCTGGAGGCCCAGGGGCAGGGGTGTGCTGACCGCGGGGGGCGCC GGGGCTGCTGCGCCTGCGGCTGCTGGAGGCCCCGGGGCAGGGGTGTGCTGACCGCGGGGGGCGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:47680824..47681161 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - 111645 RMVar_ID_111645 Human_SNP_ID_833313254 m1A Human chr19 + 19618339 19618339 19618339 GAAAATCCTTCACGCCACTGCTCGGCCCCATAAGGCCTATCCAGCCCGTTCCGTTTGAACCCCAT GAAAATCCTTCACGCCACTGCTCGGCCCCATACGGCCTATCCAGCCCGTTCCGTTTGAACCCCAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19618256..19618340 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111646 RMVar_ID_111646 Human_SNP_ID_833313870 m1A Human chr19 + 58393034 58393034 58393034 TGCCAAGTACCTGCCTCACAGTGCAGGGCGGTATGCCGCCAAACGCTTCCGCAAAGCTCAGTGTC TGCCAAGTACCTGCCTCACAGTGCAGGGCGGTGTGCCGCCAAACGCTTCCGCAAAGCTCAGTGTC A G RPS5 Ensembl:ENSG00000083845 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:58392941..58393169;chr19:58392930..58393208 26863196 MeRIP-seq:(Medium) rs759592801 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 5 liver Human_RBP_ID_528382,Human_RBP_ID_823843,Human_RBP_ID_1573697,Human_RBP_ID_4551785,Human_RBP_ID_8495807,Human_RBP_ID_9090339,Human_RBP_ID_17933140,Human_RBP_ID_18192528,Human_RBP_ID_22448039,Human_RBP_ID_22812677,Human_RBP_ID_23211049,Human_RBP_ID_23810058,Human_RBP_ID_26818029,Human_RBP_ID_27279374 Human_Splice_Rec_2051832,Human_Splice_Rec_2051842,Human_Splice_Rec_2051862,Human_Splice_Rec_2051872,Human_Splice_Rec_2051884,Human_Splice_Rec_2051888 RMVar_hsa_circ_119921,RMVar_hsa_circ_109868,RMVar_hsa_circ_92126,RMVar_hsa_circ_196514,RMVar_hsa_circ_105536,RMVar_hsa_circ_196511,RMVar_hsa_circ_196512,RMVar_hsa_circ_196510,RMVar_hsa_circ_88518,RMVar_hsa_circ_89509,RMVar_hsa_circ_196516,RMVar_hsa_circ_41293,RMVar_hsa_circ_196515,RMVar_hsa_circ_122772,RMVar_hsa_circ_274880,RMVar_hsa_circ_196518,RMVar_hsa_circ_99562,RMVar_hsa_circ_196519,RMVar_hsa_circ_196517 111647 RMVar_ID_111647 Human_SNP_ID_833316290 m1A Human chr19 - 8005597 8005597 8005597 GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCACCGCCGCCACCGCTACCGAGGCCGAGCGGAGC GAGGAGCCGCTGCCGCCGTCGCCGTCGCCGCCGCCGCCGCCACCGCTACCGAGGCCGAGCGGAGC T C ELAVL1 Ensembl:ENSG00000066044 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8005445..8005650 26863196 MeRIP-seq:(Medium) rs189171866 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_241088,Human_RBP_ID_529572,Human_RBP_ID_4555315,Human_RBP_ID_9293310,Human_RBP_ID_9328556,Human_RBP_ID_22533319 111648 RMVar_ID_111648 Human_SNP_ID_833320014 m1A Human chr19 - 50401891 50401891 50401891 AGGGGGCGCTGGGGTGTAGAAGTAGGGAGCGAAGCCGTGGATGTGGCAGCAGACAGAGAACCCCT AGGGGGCGCTGGGGTGTAGAAGTAGGGAGCGAGGCCGTGGATGTGGCAGCAGACAGAGAACCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50401776..50401932 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 111649 RMVar_ID_111649 Human_SNP_ID_833322054 m1A Human chr19 - 46196393 46196393 46196393 GACCCAGGGGCTGTGGATGGGGAATTGCTGTGATGGAGCCATGTCTGAGGAGGAGGCCAGGCATG GACCCAGGGGCTGTGGATGGGGAATTGCTGTGTTGGAGCCATGTCTGAGGAGGAGGCCAGGCATG T A IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:46196142..46196750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5588000 RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 111650 RMVar_ID_111650 Human_SNP_ID_833325005 m1A Human chr19 - 58548410 58548410 58548410 GTAATAACAGAGTGAGGTAAAGCTGGGGACCCACCAAAGGCCTCGGCACTCTTGGTCCAGGCATT GTAATAACAGAGTGAGGTAAAGCTGGGGACCCTCCAAAGGCCTCGGCACTCTTGGTCCAGGCATT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:58548276..58548425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung 111651 RMVar_ID_111651 Human_SNP_ID_833325127 m1A Human chr19 - 15264740 15264740 15264740 TGGCAGACAAAGAAGGGAGTGAAGAGGAAAGCAGACACCACCACCCCCACCACCATTGACCCCAT TGGCAGACAAAGAAGGGAGTGAAGAGGAAAGCGGACACCACCACCCCCACCACCATTGACCCCAT T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:15264639..15264824 26863196 MeRIP-seq:(Medium) rs1387038446 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_54216,Human_RBP_ID_910823,Human_RBP_ID_1067483,Human_RBP_ID_9382157,Human_RBP_ID_27816227 Human_Splice_Rec_1970612,Human_Splice_Rec_1970650,Human_Splice_Rec_1970672,Human_Splice_Rec_1970696 RMVar_hsa_circ_107707,RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193126,RMVar_hsa_circ_74882,RMVar_hsa_circ_193127,RMVar_hsa_circ_371297 111652 RMVar_ID_111652 Human_SNP_ID_833325162 m1A Human chr19 - 5221096 5221096 5221096 CCAGCAGACGGTCACCGCCTGGACTGCCTTCAACCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA CCAGCAGACGGTCACCGCCTGGACTGCCTTCAGCCTGCTCAACGGCAAGCCCAGCGTCGCCCCCA T C PTPRS Ensembl:ENSG00000105426 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:5221045..5221203 26863196 MeRIP-seq:(Medium) rs372506721 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 12 brain Human_RBP_ID_5443402,Human_RBP_ID_9292640,Human_RBP_ID_17930037,Human_RBP_ID_27470814 Human_Splice_Rec_1941803,Human_Splice_Rec_1941877,Human_Splice_Rec_1941933,Human_Splice_Rec_1941995,Human_Splice_Rec_1942049 RMVar_hsa_circ_2647,RMVar_hsa_circ_86589,RMVar_hsa_circ_107000,RMVar_hsa_circ_111781,RMVar_hsa_circ_109409,RMVar_hsa_circ_191668,RMVar_hsa_circ_191666,RMVar_hsa_circ_191667,RMVar_hsa_circ_191665,RMVar_hsa_circ_17605,RMVar_hsa_circ_3453,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_191678,RMVar_hsa_circ_100274,RMVar_hsa_circ_346716,RMVar_hsa_circ_95070,RMVar_hsa_circ_191683,RMVar_hsa_circ_96530,RMVar_hsa_circ_191686,RMVar_hsa_circ_191687,RMVar_hsa_circ_341630,RMVar_hsa_circ_298835,RMVar_hsa_circ_191688 111653 RMVar_ID_111653 Human_SNP_ID_833325374 m1A Human chr19 + 49594542 49594542 49594542 GCCTCCGTCATGAACCTTATCTCGGCCCTGGAATCCCGGGGCCCCCAGCCTGGCCCCTCCGCCTC GCCTCCGTCATGAACCTTATCTCGGCCCTGGAGTCCCGGGGCCCCCAGCCTGGCCCCTCCGCCTC A G PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49594501..49594550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus Human_RBP_ID_525428,Human_RBP_ID_4542338,Human_RBP_ID_17501185,Human_RBP_ID_27277094,Human_RBP_ID_27470353 Human_Splice_Rec_2031186,Human_Splice_Rec_2031187 Human_miRNA_ID_1233971,Human_miRNA_ID_2296392,Human_miRNA_ID_2682156,Human_miRNA_ID_2686338 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111654 RMVar_ID_111654 Human_SNP_ID_833328088 m1A Human chr19 - 18994426 18994426 18994426 GGTGCTGACGGGCAGGAGCACAAAGAAGACACATTCGATGTGTTCCGACAGAGGATGATGCAGAT GGTGCTGACGGGCAGGAGCACAAAGAAGACACGTTCGATGTGTTCCGACAGAGGATGATGCAGAT T C SUGP2 Ensembl:ENSG00000064607 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:18994401..18994425 32194978 MeRIP-seq:(Medium) rs1443942341 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_54858,Human_RBP_ID_1881305,Human_RBP_ID_4511496,Human_RBP_ID_9380824,Human_RBP_ID_13398297,Human_RBP_ID_25440734 Human_Splice_Rec_1981854,Human_Splice_Rec_1981855,Human_Splice_Rec_1981877,Human_Splice_Rec_1981904,Human_Splice_Rec_1981905,Human_Splice_Rec_1981926,Human_Splice_Rec_1981927,Human_Splice_Rec_1981946,Human_Splice_Rec_1981947,Human_Splice_Rec_1981971,Human_Splice_Rec_1981990,Human_Splice_Rec_1982008,Human_Splice_Rec_1982016,Human_Splice_Rec_1982017 RMVar_hsa_circ_47792,RMVar_hsa_circ_54514,RMVar_hsa_circ_73962,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_46519,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 111655 RMVar_ID_111655 Human_SNP_ID_833335299 m1A Human chr19 - 17274026 17274026 17274026 ACCCCAGGGCACCCAGCGCCTGCCGCAGCCTCACCCAGGCCGTGTCATCGTTCACCACCACCAGT ACCCCAGGGCACCCAGCGCCTGCCGCAGCCTCGCCCAGGCCGTGTCATCGTTCACCACCACCAGT T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:17273976..17276537 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine 111656 RMVar_ID_111656 Human_SNP_ID_833337058 m1A Human chr19 + 1612410 1612410 1612410 GCCTCTCCCGGTCCCTCAGGTCTTTCTCCTCCAGGGACAGCACCTCGTCCGTACTGCTGGGTCAC GCCTCTCCCGGTCCCTCAGGTCTTTCTCCTCCCGGGACAGCACCTCGTCCGTACTGCTGGGTCAC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:1612326..1612450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 111657 RMVar_ID_111657 Human_SNP_ID_833337656 m1A Human chr19 - 49086453 49086453 49086453 GGTGGCAGGTATGGAATAGGGTCACGGGGGGCAAAGAGGGCCAGAAGGTTGGGCGGCAGGAACTG GGTGGCAGGTATGGAATAGGGTCACGGGGGGCGAAGAGGGCCAGAAGGTTGGGCGGCAGGAACTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr19:49086401..49086575;chr19:49086401..49086500 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 111658 RMVar_ID_111658 Human_SNP_ID_833337867 m1A Human chr19 + 10682595 10682595 10682595 GGGTGCTGAAGGCAGGGACTCGAGCAAGGGGGAGGACTCGGCTGAGGAGACCGAGGCGAAGCCAG GGGTGCTGAAGGCAGGGACTCGAGCAAGGGGGGGGACTCGGCTGAGGAGACCGAGGCGAAGCCAG A G ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10682524..10682742 26863196 MeRIP-seq:(Medium) rs1422037785 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_53783,Human_RBP_ID_240135,Human_RBP_ID_771435,Human_RBP_ID_825410,Human_RBP_ID_913243,Human_RBP_ID_1879633,Human_RBP_ID_3562400,Human_RBP_ID_3954450,Human_RBP_ID_4499016,Human_RBP_ID_5375661,Human_RBP_ID_6717628,Human_RBP_ID_9293377,Human_RBP_ID_9380465,Human_RBP_ID_13359958,Human_RBP_ID_17914320,Human_RBP_ID_18994317,Human_RBP_ID_22977648,Human_RBP_ID_26335652,Human_RBP_ID_27462837 Human_Splice_Rec_1955734,Human_Splice_Rec_1955770,Human_Splice_Rec_1955810,Human_Splice_Rec_1955844,Human_Splice_Rec_1955930,Human_Splice_Rec_1955962,Human_Splice_Rec_1955992,Human_Splice_Rec_1956028 RMVar_hsa_circ_50296,RMVar_hsa_circ_92401,RMVar_hsa_circ_192412,RMVar_hsa_circ_93559,RMVar_hsa_circ_100977,RMVar_hsa_circ_192416,RMVar_hsa_circ_192415,RMVar_hsa_circ_5258,RMVar_hsa_circ_14614,RMVar_hsa_circ_362879,RMVar_hsa_circ_192418,RMVar_hsa_circ_98084 111659 RMVar_ID_111659 Human_SNP_ID_833338731 m1A Human chr19 + 18175190 18175190 18175190 TCCCAACATGGCTGTTGGTCATGGAGATCCTCAATGTCACGCTGGTGCCCTACGGAAACGCACAG TCCCAACATGGCTGTTGGTCATGGAGATCCTCCATGTCACGCTGGTGCCCTACGGAAACGCACAG A C IFI30,AC007192.1 Ensembl:ENSG00000216490,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18175142..18177190 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_516042,Human_RBP_ID_9329901,Human_RBP_ID_18724433,Human_RBP_ID_22762876,Human_RBP_ID_26815508 Human_Splice_Rec_1979319,Human_Splice_Rec_1979469,Human_Splice_Rec_1979479 RMVar_hsa_circ_78293,RMVar_hsa_circ_78260,RMVar_hsa_circ_193436,RMVar_hsa_circ_127358,RMVar_hsa_circ_120660,RMVar_hsa_circ_193438,RMVar_hsa_circ_193440,RMVar_hsa_circ_91583,RMVar_hsa_circ_193441,RMVar_hsa_circ_79824,RMVar_hsa_circ_84904,RMVar_hsa_circ_102905,RMVar_hsa_circ_193442,RMVar_hsa_circ_193446,RMVar_hsa_circ_79374,RMVar_hsa_circ_193445,RMVar_hsa_circ_88153,RMVar_hsa_circ_104394,RMVar_hsa_circ_114247,RMVar_hsa_circ_193447,RMVar_hsa_circ_193448,RMVar_hsa_circ_193450,RMVar_hsa_circ_85983,RMVar_hsa_circ_193449,RMVar_hsa_circ_116562,RMVar_hsa_circ_288218,RMVar_hsa_circ_193451,RMVar_hsa_circ_124717,RMVar_hsa_circ_96104,RMVar_hsa_circ_193453,RMVar_hsa_circ_193455,RMVar_hsa_circ_16923,RMVar_hsa_circ_193456,RMVar_hsa_circ_193454,RMVar_hsa_circ_193452 111660 RMVar_ID_111660 Human_SNP_ID_833338779 m1A Human chr19 + 7643773 7643773 7643773 CTTGGAGAGGTGGGACCTGGGTGAGGGGTGGAACCTTGGAGAGGTGGGACCTGGATGAGGGGTGG CTTGGAGAGGTGGGACCTGGGTGAGGGGTGGAGCCTTGGAGAGGTGGGACCTGGATGAGGGGTGG A G STXBP2 Ensembl:ENSG00000076944 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:7643401..7643918 26863196 MeRIP-seq:(Medium) rs968114861 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 liver,haematopoietic and lymphoid tissue Human_RBP_ID_7484,Human_RBP_ID_263170,Human_RBP_ID_769481,Human_RBP_ID_3580769,Human_RBP_ID_3954336,Human_RBP_ID_5321351,Human_RBP_ID_5369874,Human_RBP_ID_8100310,Human_RBP_ID_8196041,Human_RBP_ID_8233068,Human_RBP_ID_8942409,Human_RBP_ID_9346669,Human_RBP_ID_9425928,Human_RBP_ID_19091959,Human_RBP_ID_21977609,Human_RBP_ID_22426326,Human_RBP_ID_22591014,Human_RBP_ID_22718311,Human_RBP_ID_26335422,Human_RBP_ID_27839249 RMVar_hsa_circ_126911,RMVar_hsa_circ_192017 111661 RMVar_ID_111661 Human_SNP_ID_833339028 m1A Human chr19 + 46922262 46922262 46922262 CATCCGGAAGAAAGAGGAGGATCAGGCATCCCAGGGTTATAAAGGGGACAATGCTGTCATTCCAT CATCCGGAAGAAAGAGGAGGATCAGGCATCCCTGGGTTATAAAGGGGACAATGCTGTCATTCCAT A T ARHGAP35 Ensembl:ENSG00000160007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46922213..46922278 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_6775423,Human_RBP_ID_22359063 Human_Splice_Rec_2023191,Human_Splice_Rec_2023201,Human_Splice_Rec_2023211 RMVar_hsa_circ_90622,RMVar_hsa_circ_195532,RMVar_hsa_circ_195533 111662 RMVar_ID_111662 Human_SNP_ID_833339197 m1A Human chr19 - 48993925 48993925 48993925 GCTCGCTCCTCACCCTCCATGCACCCACACTTACAACGGTTGCCATGATGCTCACCAACTGCCAG GCTCGCTCCTCACCCTCCATGCACCCACACTTCCAACGGTTGCCATGATGCTCACCAACTGCCAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48993876..48994245;chr19:48993876..48994149;chr19:48993851..48994076 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 111663 RMVar_ID_111663 Human_SNP_ID_833343451 m1A Human chr19 + 48872610 48872610 48872610 GTCCGGACCTGTGATCGCTTCTGGCAGACCGAACCGGCGCTCCTGCCCCCGGGGTGACGCGCAGC GTCCGGACCTGTGATCGCTTCTGGCAGACCGACCCGGCGCTCCTGCCCCCGGGGTGACGCGCAGC A C PPP1R15A Ensembl:ENSG00000087074 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:48872426..48872650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4541240,Human_RBP_ID_9382742 Human_Splice_Rec_2027831 111664 RMVar_ID_111664 Human_SNP_ID_833343533 m1A Human chr19 - 45815948 45815948 45815948 GGAAGCCATGGATTTCCGGGAGGAGGGGCCTGAGTGCGAGACCCCGGGCATCTTCATCAGCATGG GGAAGCCATGGATTTCCGGGAGGAGGGGCCTGTGTGCGAGACCCCGGGCATCTTCATCAGCATGG T A SYMPK Ensembl:ENSG00000125755 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45815926..45815950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_5117760,Human_RBP_ID_6774003,Human_RBP_ID_8835511,Human_RBP_ID_17928024,Human_RBP_ID_18166078,Human_RBP_ID_18735988,Human_RBP_ID_18995153,Human_RBP_ID_23131495 Human_Splice_Rec_2021047,Human_Splice_Rec_2021099,Human_Splice_Rec_2021149,Human_Splice_Rec_2021199,Human_Splice_Rec_2021205 RMVar_hsa_circ_266027 111665 RMVar_ID_111665 Human_SNP_ID_833353948 m1A Human chr19 + 47417345 47417345 47417345 CCATCCACGATGCCTGGGTAGTGCGGCAGCTCATCATACTGGGGGAAGGTGAGAAGAGAAGGGCG CCATCCACGATGCCTGGGTAGTGCGGCAGCTCGTCATACTGGGGGAAGGTGAGAAGAGAAGGGCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47416929..47417393 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 6 pancreas 111666 RMVar_ID_111666 Human_SNP_ID_833357789 m1A Human chr19 - 47209211 47209211 47209211 GGCCAAGGCACTCCACAATCCCATTCCCCTTCATGCCATCGAAGAAGAAGAAGTTGTTGTGAGGA GGCCAAGGCACTCCACAATCCCATTCCCCTTCGTGCCATCGAAGAAGAAGAAGTTGTTGTGAGGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47197226..47209375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 111667 RMVar_ID_111667 Human_SNP_ID_833362413 m1A Human chr19 - 17395367 17395367 17395367 GGCCCTGCGATGGGAATGCACTTGGTGGAAGAACCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA GGCCCTGCGATGGGAATGCACTTGGTGGAAGAGCCTTGGGGAGGCTACAGGAAGGAGTGAAAAGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:17395250..17395453;chr19:17395001..17395549 26863196 MeRIP-seq:(Medium) rs8106139 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_6618,GWAS_ID_6619,GWAS_ID_6620,GWAS_ID_6621,GWAS_ID_6622,GWAS_ID_6623,GWAS_ID_6624 111668 RMVar_ID_111668 Human_SNP_ID_833364681 m1A Human chr19 - 984453 984453 984453 CAGGCCGCGGGGTCCCGCCTGGCCGCCGCGGTAGGTGAGCAGGTTGGCGCCCGAGTGAAGTTCCC CAGGCCGCGGGGTCCCGCCTGGCCGCCGCGGTGGGTGAGCAGGTTGGCGCCCGAGTGAAGTTCCC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:984351..985916 26863410 MeRIP-seq:(Medium) rs748069476 Functional Loss SNV ICGC 33..33 33 THCA 1 - 111669 RMVar_ID_111669 Human_SNP_ID_833368569 m1A Human chr19 - 39470492 39470492 39470492 CCTGGAAGGTCTCCCGTTCTAGTCGCACGATGACACCCACAGTCTGGGGATCCAGCTGCACCAGC CCTGGAAGGTCTCCCGTTCTAGTCGCACGATGGCACCCACAGTCTGGGGATCCAGCTGCACCAGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:39470442..39470562 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 111670 RMVar_ID_111670 Human_SNP_ID_833371054 m1A Human chr19 - 10308182 10308182 10308182 CTCCAGCCTGCAGATCATCCCCACGTACAGGTAGGGGCCGGCTGGGGCCAGGCCGCCCTTTCTCC CTCCAGCCTGCAGATCATCCCCACGTACAGGTTGGGGCCGGCTGGGGCCAGGCCGCCCTTTCTCC T A AC011511.1,ZGLP1 Ensembl:ENSG00000167807,Ensembl:ENSG00000220201 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10308179..10308259 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 6 ovary 111671 RMVar_ID_111671 Human_SNP_ID_833374550 m1A Human chr19 - 43592858 43592858 43592858 GGATCCGGAGTGTCTGGGAGAAGGCAAGATGGAGAATCCCAAGGGCGAGAGCTTAAAGAACGCAG GGATCCGGAGTGTCTGGGAGAAGGCAAGATGGTGAATCCCAAGGGCGAGAGCTTAAAGAACGCAG T A IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding CDS,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:43592791..43593240 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_6767993 111672 RMVar_ID_111672 Human_SNP_ID_833374782 m1A Human chr19 - 10681050 10681050 10681050 AAGGCAGAGGGTCCATGCCTAGGACTTTATGGAGCTGGCCGAAGGCAGCGAGCCGCAGTGCGTGC AAGGCAGAGGGTCCATGCCTAGGACTTTATGGGGCTGGCCGAAGGCAGCGAGCCGCAGTGCGTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10681001..10681050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 7 brain 111673 RMVar_ID_111673 Human_SNP_ID_833377334 m1A Human chr19 + 49158228 49158228 49158228 GGATCCCCAAGATCTTCAAGAAGAAGACCTGCACGACGTTCATAGTTGACTCCACAGATCCGGGG GGATCCCCAAGATCTTCAAGAAGAAGACCTGCGCGACGTTCATAGTTGACTCCACAGATCCGGGG A G TRPM4 Ensembl:ENSG00000130529 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49158156..49158228 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck superficial_spreading,skin superficial_spreading 3 skin,head and neck Human_Splice_Rec_2029054,Human_Splice_Rec_2029055,Human_Splice_Rec_2029062,Human_Splice_Rec_2029063,Human_Splice_Rec_2029100,Human_Splice_Rec_2029102,Human_Splice_Rec_2029103,Human_Splice_Rec_2029150,Human_Splice_Rec_2029151,Human_Splice_Rec_2029194,Human_Splice_Rec_2029195,Human_Splice_Rec_2029240,Human_Splice_Rec_2029241,Human_Splice_Rec_2029286,Human_Splice_Rec_2029287 111674 RMVar_ID_111674 Human_SNP_ID_833378154 m1A Human chr19 - 33493339 33493339 33493339 CCTCTAAAGTGGGTTTTTCTTTCCGACCTTCTAGATTGCCAGCGTCCTGACGTCACAGAAGCCCT CCTCTAAAGTGGGTTTTTCTTTCCGACCTTCTGGATTGCCAGCGTCCTGACGTCACAGAAGCCCT T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:33493276..33493350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_Splice_Rec_1990099,Human_Splice_Rec_1990127,Human_Splice_Rec_1990163,Human_Splice_Rec_1990183,Human_Splice_Rec_1990211,Human_Splice_Rec_1990249,Human_Splice_Rec_1990283,Human_Splice_Rec_1990291,Human_Splice_Rec_1990303 RMVar_hsa_circ_105045,RMVar_hsa_circ_194024,RMVar_hsa_circ_353639,RMVar_hsa_circ_374786,RMVar_hsa_circ_359445,RMVar_hsa_circ_375369,RMVar_hsa_circ_194026,RMVar_hsa_circ_194027 111675 RMVar_ID_111675 Human_SNP_ID_833385784 m1A Human chr19 + 10671158 10671158 10671158 GGAAAAGGGTAGCAGCGAGCAGGCAGAGTCCGATAACATGGATGTGCCCCCAGAGGACGACAGTA GGAAAAGGGTAGCAGCGAGCAGGCAGAGTCCGGTAACATGGATGTGCCCCCAGAGGACGACAGTA A G ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10671107..10671454 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_53760,Human_RBP_ID_512308,Human_RBP_ID_771421,Human_RBP_ID_825395,Human_RBP_ID_913225,Human_RBP_ID_1553700,Human_RBP_ID_1879580,Human_RBP_ID_3954438,Human_RBP_ID_6717491,Human_RBP_ID_8476299,Human_RBP_ID_8839082,Human_RBP_ID_9084273,Human_RBP_ID_9258953,Human_RBP_ID_9380441,Human_RBP_ID_13359455,Human_RBP_ID_18165956,Human_RBP_ID_18440443,Human_RBP_ID_22501520,Human_RBP_ID_22808923,Human_RBP_ID_22966372,Human_RBP_ID_23781114,Human_RBP_ID_24545707,Human_RBP_ID_26334834 Human_Splice_Rec_1955715,Human_Splice_Rec_1955753,Human_Splice_Rec_1955791,Human_Splice_Rec_1955825,Human_Splice_Rec_1955861,Human_Splice_Rec_1955869,Human_Splice_Rec_1955875,Human_Splice_Rec_1955891,Human_Splice_Rec_1955903,Human_Splice_Rec_1955911,Human_Splice_Rec_1955943,Human_Splice_Rec_1955973,Human_Splice_Rec_1956009,Human_Splice_Rec_1956043,Human_Splice_Rec_1956057 RMVar_hsa_circ_4376,RMVar_hsa_circ_302792,RMVar_hsa_circ_362795,RMVar_hsa_circ_50296,RMVar_hsa_circ_14966,RMVar_hsa_circ_92401,RMVar_hsa_circ_108280,RMVar_hsa_circ_192411,RMVar_hsa_circ_192412 111676 RMVar_ID_111676 Human_SNP_ID_833385958 m1A Human chr19 - 1242421 1242421 1242421 GCAGACAACAGCGTGGGGAATGATGGCGGGGCAGGCCGGCCCCGCGCCCACCGGGCACTCGGCCT GCAGACAACAGCGTGGGGAATGATGGCGGGGCCGGCCGGCCCCGCGCCCACCGGGCACTCGGCCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:1242406..1242657 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas RMVar_hsa_circ_191022 111677 RMVar_ID_111677 Human_SNP_ID_833393175 m1A Human chr19 - 40682918 40682918 40682918 GTAGAGGAGTCCCGGGGAATGCACGTGTGTGAAGATGCGGTGAAGAAGCTGAAGGCGGTGAGTGA GTAGAGGAGTCCCGGGGAATGCACGTGTGTGACGATGCGGTGAAGAAGCTGAAGGCGGTGAGTGA T G NUMBL Ensembl:ENSG00000105245 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:40681049..40684106 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_3957004,Human_RBP_ID_23798264,Human_RBP_ID_26336319 Human_Splice_Rec_2009510,Human_Splice_Rec_2009511,Human_Splice_Rec_2009526,Human_Splice_Rec_2009527,Human_Splice_Rec_2009542,Human_Splice_Rec_2009543,Human_Splice_Rec_2009555,Human_Splice_Rec_2009574,Human_Splice_Rec_2009575,Human_Splice_Rec_2009586,Human_Splice_Rec_2009587,Human_Splice_Rec_2009592,Human_Splice_Rec_2009593,Human_Splice_Rec_2009602,Human_Splice_Rec_2009603 RMVar_hsa_circ_24238,RMVar_hsa_circ_57324 111678 RMVar_ID_111678 Human_SNP_ID_833397086 m1A Human chr19 + 19009958 19009958 19009958 GGGCCTGAGGCTTCTAAGCTGGGGTCCTGAGGAGAAGGTCCAACTGGGTCTGGCGGGCAGTCCTT GGGCCTGAGGCTTCTAAGCTGGGGTCCTGAGGTGAAGGTCCAACTGGGTCTGGCGGGCAGTCCTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:19009855..19010269 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111679 RMVar_ID_111679 Human_SNP_ID_833398168 m1A Human chr19 - 41310306 41310306 41310306 CCGCCGTCGCCGTCGCCACGGCCTCCATCCTGATTCTCTCGGACTTTTCAACCGCCCGGCGGGCC CCGCCGTCGCCGTCGCCACGGCCTCCATCCTGTTTCTCTCGGACTTTTCAACCGCCCGGCGGGCC T A AC011462.5,TGFB1 Ensembl:ENSG00000286177,Ensembl:ENSG00000105329 lincRNA,Protein coding exon,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:41310201..41310394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 111680 RMVar_ID_111680 Human_SNP_ID_833408418 m1A Human chr19 - 49650975 49650975 49650975 AGGGGAGGAAGATGAGGGAGAAGGGGAAGGGGAGGAGGATGCAGAGGAGGGGGCAGGGGGTGGGG AGGGGAGGAAGATGAGGGAGAAGGGGAAGGGGGGGAGGATGCAGAGGAGGGGGCAGGGGGTGGGG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:49650886..49650974 26863410 MeRIP-seq:(Medium) rs1328484150 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 2 oesophagus 111681 RMVar_ID_111681 Human_SNP_ID_833412633 m1A Human chr19 + 49682245 49682242 49682245 CTCTGATTATGCGGTGAAGATCGTCAAAGCCAACAAGTTAGACCACGGTGAGCCCAGAAAGAGGA CTCTGATTATGCGGTGAAGATCGTCAAAGC___CAAGTTAGACCACGGTGAGCCCAGAAAGAGGA CCAA C PRMT1 Ensembl:ENSG00000126457 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:49682176..49682275 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 COCA 1 - Human_RBP_ID_525502,Human_RBP_ID_1569790,Human_RBP_ID_1890998,Human_RBP_ID_3957367,Human_RBP_ID_13496847,Human_RBP_ID_18737649,Human_RBP_ID_18995300,Human_RBP_ID_22448957,Human_RBP_ID_23211356 Human_Splice_Rec_2031672,Human_Splice_Rec_2031673,Human_Splice_Rec_2031684,Human_Splice_Rec_2031685,Human_Splice_Rec_2031702,Human_Splice_Rec_2031703,Human_Splice_Rec_2031720,Human_Splice_Rec_2031721,Human_Splice_Rec_2031732,Human_Splice_Rec_2031733,Human_Splice_Rec_2031750,Human_Splice_Rec_2031751,Human_Splice_Rec_2031766,Human_Splice_Rec_2031767,Human_Splice_Rec_2031774,Human_Splice_Rec_2031775,Human_Splice_Rec_2031790,Human_Splice_Rec_2031791,Human_Splice_Rec_2031808,Human_Splice_Rec_2031809,Human_Splice_Rec_2031820,Human_Splice_Rec_2031821,Human_Splice_Rec_2031834,Human_Splice_Rec_2031840,Human_Splice_Rec_2031841,Human_Splice_Rec_2031850 RMVar_hsa_circ_104811,RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,RMVar_hsa_circ_195904,RMVar_hsa_circ_127875,RMVar_hsa_circ_102156,RMVar_hsa_circ_195911,RMVar_hsa_circ_195906,RMVar_hsa_circ_195908,RMVar_hsa_circ_195909,RMVar_hsa_circ_195907,RMVar_hsa_circ_297570,RMVar_hsa_circ_317798,RMVar_hsa_circ_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_304264,RMVar_hsa_circ_195912,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 111682 RMVar_ID_111682 Human_SNP_ID_833414632 m1A Human chr19 - 49720053 49720053 49720053 CAACATGCCAGTGGCCCGGAGCTGGGTTTGTCACAAAACTTATGTGACCCCGCGGAGACCCTTCG CAACATGCCAGTGGCCCGGAGCTGGGTTTGTCGCAAAACTTATGTGACCCCGCGGAGACCCTTCG T C AC011495.1 Ensembl:ENSG00000243829 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879196815 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_21892354 Human_miRNA_ID_1908237 111683 RMVar_ID_111683 Human_SNP_ID_833416972 m1A Human chr19 - 38846043 38846043 38846043 GCCTAAAAAGAGACAAGCACTGGTGGAGTTTGAAGATGTGTTGGGGGCTTGCAACGCAGTGAACT GCCTAAAAAGAGACAAGCACTGGTGGAGTTTGGAGATGTGTTGGGGGCTTGCAACGCAGTGAACT T C HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:38846001..38846075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_52973,Human_RBP_ID_1887165,Human_RBP_ID_9380984,Human_RBP_ID_24484334,Human_RBP_ID_26334914 Human_Splice_Rec_2003974,Human_Splice_Rec_2003994,Human_Splice_Rec_2004024,Human_Splice_Rec_2004046,Human_Splice_Rec_2004092,Human_Splice_Rec_2004116,Human_Splice_Rec_2004126,Human_Splice_Rec_2004134,Human_Splice_Rec_2004142,Human_Splice_Rec_2004146 RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_58914,RMVar_hsa_circ_313839,RMVar_hsa_circ_322096,RMVar_hsa_circ_194683,RMVar_hsa_circ_194684,RMVar_hsa_circ_372195,RMVar_hsa_circ_194685 111684 RMVar_ID_111684 Human_SNP_ID_833417996 m1A Human chr19 + 3529709 3529697 3529709 TGGTTGAGGGAGTGGATGGTTGAGCGGATGGGAGAGCGGATGGGAGAGTGGATGGGAGAGTGGAT TGGTTGAGGGAGTGGATGGTT____________GAGCGGATGGGAGAGTGGATGGGAGAGTGGAT TGAGCGGATGGGA T FZR1 Ensembl:ENSG00000105325 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3529701..3529725 26863196 MeRIP-seq:(Medium) rs1187922209 Functional Loss DEL ICGC 22..33 33 PBCA 1 - Human_RBP_ID_5292613,Human_RBP_ID_5649712,Human_RBP_ID_23793145 RMVar_hsa_circ_191347,RMVar_hsa_circ_90867,RMVar_hsa_circ_364580,RMVar_hsa_circ_105969,RMVar_hsa_circ_265827,RMVar_hsa_circ_191351 111685 RMVar_ID_111685 Human_SNP_ID_833419407 m1A Human chr19 - 12769981 12769981 12769981 GAGGGAGCTGCGGCGGCAGGTGCGGCAGCTGGAGGAACGCAACGCCGGCCACGCCGAGCGCACGC GAGGGAGCTGCGGCGGCAGGTGCGGCAGCTGGTGGAACGCAACGCCGGCCACGCCGAGCGCACGC T A HOOK2 Ensembl:ENSG00000095066 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12769930..12770024 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_18996773,Human_RBP_ID_22977416,Human_RBP_ID_27816131 RMVar_hsa_circ_75656,RMVar_hsa_circ_192784,RMVar_hsa_circ_326967 111686 RMVar_ID_111686 Human_SNP_ID_833426554 m1A Human chr19 + 49867157 49867157 49867157 TCCGAGGGCAGGAAGATGGGGGGCGCTCCCCCAGGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC TCCGAGGGCAGGAAGATGGGGGGCGCTCCCCCGGGGGGGCTCTCGAGCCACAAGCGGCCCGGGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49867112..49867250 26863196 MeRIP-seq:(Medium) rs765919999 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,lung squamous_cell_carcinoma,breast metaplastic_carcinoma,lung adenocarcinoma,right_upper_lobe adenocarcinoma 31 lung,breast 111687 RMVar_ID_111687 Human_SNP_ID_833428866 m1A Human chr19 + 15432408 15432408 15432408 CCGGCAGGCGGGATTCCGACCTTCCCCTCCCCACACCCTCCCAAGCGCGGGCTCTTACCGGGCGC CCGGCAGGCGGGATTCCGACCTTCCCCTCCCCCCACCCTCCCAAGCGCGGGCTCTTACCGGGCGC A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:15432403..15432656 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111688 RMVar_ID_111688 Human_SNP_ID_833429334 m1A Human chr19 + 572628 572628 572628 AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATAGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT AGCGGTTGGAGGTTGTAGGACCGGCGAGGAATGGGAATCATGGCGGCTGCGCTGTTCGTGCTGCT A G BSG Ensembl:ENSG00000172270 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:572601..572814 26863196 MeRIP-seq:(Medium) rs12609610 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_RBP_ID_527547,Human_RBP_ID_1572151,Human_RBP_ID_4549119,Human_RBP_ID_5319662,Human_RBP_ID_5500220,Human_RBP_ID_6786275,Human_RBP_ID_8494652,Human_RBP_ID_9327907,Human_RBP_ID_13516791,Human_RBP_ID_18191511,Human_RBP_ID_22069333,Human_RBP_ID_22446237,Human_RBP_ID_25435042,Human_RBP_ID_26470397,Human_RBP_ID_26769705,Human_RBP_ID_26995957,Human_RBP_ID_27471685 Human_Splice_Rec_1928489,Human_Splice_Rec_1928491,Human_Splice_Rec_1928499,Human_Splice_Rec_1928513,Human_Splice_Rec_1928517,Human_Splice_Rec_1928519,Human_Splice_Rec_1928529,Human_Splice_Rec_1928545,Human_Splice_Rec_1928553,Human_Splice_Rec_1928563 GWAS_ID_9598,GWAS_ID_9599 RMVar_hsa_circ_111780,RMVar_hsa_circ_190861 111689 RMVar_ID_111689 Human_SNP_ID_833431049 m1A Human chr19 - 1918280 1918280 1918280 TGCAGACGGCCCCCGGCAGCTCTGCTCACCGGAAGGCCTTGTAGACAGGCCGGAACCAGCACACG TGCAGACGGCCCCCGGCAGCTCTGCTCACCGGCAGGCCTTGTAGACAGGCCGGAACCAGCACACG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1918239..1919127 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 111690 RMVar_ID_111690 Human_SNP_ID_833433127 m1A Human chr19 + 4408880 4408880 4408880 TGAGTGGTTGTAACTTTAAACGTTCACTAGAGATGGCTTTCTGTCTTTGTTTCAGCCCGTCTGCC TGAGTGGTTGTAACTTTAAACGTTCACTAGAGTTGGCTTTCTGTCTTTGTTTCAGCCCGTCTGCC A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4408877..4409122 26863196 MeRIP-seq:(Medium) rs1278992706 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas Human_Splice_Rec_1940042 RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_117327,RMVar_hsa_circ_294806,RMVar_hsa_circ_191530,RMVar_hsa_circ_291666,RMVar_hsa_circ_89465,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_191531 111691 RMVar_ID_111691 Human_SNP_ID_833435214 m1A Human chr19 - 9044045 9044044 9044045 GCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAGGAAGGGAAAAAAAAAGCTCAGTTTCGGAGGT GCGACAGAGTGAGACTCTGTCTCAAAAAAAAA_GGAAGGGAAAAAAAAAGCTCAGTTTCGGAGGT CT C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:9044019..9044106 26863410 MeRIP-seq:(Medium) rs991693169 Functional Loss DEL ICGC 33..33 33 COCA 1 - 111692 RMVar_ID_111692 Human_SNP_ID_833436490 m1A Human chr19 - 15255422 15255422 15255422 GGGCCGCGTGGTGCACATCATCCAGTCACGGGAGCCCTCCCTGAAGAATTCCAACCCCGACGAGA GGGCCGCGTGGTGCACATCATCCAGTCACGGGCGCCCTCCCTGAAGAATTCCAACCCCGACGAGA T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15254146..15255581 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_54211,Human_RBP_ID_5131089,Human_RBP_ID_9380697,Human_RBP_ID_24545453,Human_RBP_ID_26334883 Human_miRNA_ID_1370328,Human_miRNA_ID_2030593,Human_miRNA_ID_2691039,Human_miRNA_ID_2694361 RMVar_hsa_circ_45550,RMVar_hsa_circ_352477,RMVar_hsa_circ_9407,RMVar_hsa_circ_193124,RMVar_hsa_circ_372033 111693 RMVar_ID_111693 Human_SNP_ID_833437101 m1A Human chr19 - 5719748 5719748 5719748 CCGATGTGTTTCCGCACCTGCCGCTCATCGCCATCACCCGCAACCCGGTGTTCCCGCGCTTTATC CCGATGTGTTTCCGCACCTGCCGCTCATCGCCGTCACCCGCAACCCGGTGTTCCCGCGCTTTATC T C LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:5719726..5719750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 5 lung Human_RBP_ID_4549093,Human_RBP_ID_18740147,Human_RBP_ID_22070775,Human_RBP_ID_27471682 Human_Splice_Rec_1942781,Human_Splice_Rec_1942811,Human_Splice_Rec_1942845,Human_Splice_Rec_1942880,Human_Splice_Rec_1942881,Human_Splice_Rec_1942915,Human_Splice_Rec_1942983,Human_Splice_Rec_1943037,Human_Splice_Rec_1943055,Human_Splice_Rec_1943057 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 111694 RMVar_ID_111694 Human_SNP_ID_833442628 m1A Human chr19 - 48999375 48999375 48999375 GGCTTAGGTCCTATTCCTGACCCAACTCACTCACCGATTCGCTCAATCCTTGTTACATCACGGAT GGCTTAGGTCCTATTCCTGACCCAACTCACTCGCCGATTCGCTCAATCCTTGTTACATCACGGAT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48999326..48999375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111695 RMVar_ID_111695 Human_SNP_ID_833444134 m1A Human chr19 + 49560034 49560018 49560034 GCTCAGTCGAATGTTCTGGGTCCCATAGCCCGAGGCCGCTGGGGACAGAGATGGGCAGAGTGATG GCTCAGTCGAATGTTCT________________GGCCGCTGGGGACAGAGATGGGCAGAGTGATG TGGGTCCCATAGCCCGA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:49559884..49560092;chr19:49559882..49560081;chr19:49559874..49560103 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 18..33 33 LIHC 1 - 111696 RMVar_ID_111696 Human_SNP_ID_833445958 m1A Human chr19 + 42294913 42294910 42294913 GTCTGCAGTTGAAGATCCGTGAGGTGCGCCAGAAGATCATGCAGGCTGCCACTCCCACGGAGCAG GTCTGCAGTTGAAGATCCGTGAGGTGCGCC___AGATCATGCAGGCTGCCACTCCCACGGAGCAG CAGA C CIC Ensembl:ENSG00000079432 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:42294904..42295124 26863196 MeRIP-seq:(Medium) rs751580245 Functional Loss DEL TCGA 31..33 33 LGG 1 - Human_RBP_ID_522775 Human_Splice_Rec_2013782,Human_Splice_Rec_2013822,Human_Splice_Rec_2013860,Human_Splice_Rec_2013868,Human_Splice_Rec_2013876,Human_Splice_Rec_2013884,Human_Splice_Rec_2013886 RMVar_hsa_circ_109072,RMVar_hsa_circ_195085,RMVar_hsa_circ_119989,RMVar_hsa_circ_195091 111697 RMVar_ID_111697 Human_SNP_ID_833451263 m1A Human chr19 + 58516531 58516507 58516531 GGGGTGCCTGAGGGGGCCGTGGTGGGAGCAGCAGAGGGAGCCGGGACCTCCCCCAGCTGAGTACT GGGGTGCCT________________________GAGGGAGCCGGGACCTCCCCCAGCTGAGTACT TGAGGGGGCCGTGGTGGGAGCAGCA T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:58516480..58516564 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 10..33 33 BLCA 1 - 111698 RMVar_ID_111698 Human_SNP_ID_833451993 m1A Human chr19 - 38840216 38840216 38840216 CCCCAGTATGGGCACCCCCCACCCCCTCCCCCACCACCCGAGTATGGCCCTCACGCCGACAGCCC CCCCAGTATGGGCACCCCCCACCCCCTCCCCCCCCACCCGAGTATGGCCCTCACGCCGACAGCCC T G HNRNPL Ensembl:ENSG00000104824 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1441410370 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,liver hepatocellular_carcinoma 4 liver,head and neck Human_miRNA_ID_1703594 RMVar_hsa_circ_12312,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_107929,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676,RMVar_hsa_circ_194678,RMVar_hsa_circ_358577 111699 RMVar_ID_111699 Human_SNP_ID_833452366 m1A Human chr19 + 39386354 39386354 39386354 TCCTCCCGTTCACTCTCGCTGCCCGAGTGCTCATCTTCACTGCCCTCCTTCTCACTGCTGCTGCC TCCTCCCGTTCACTCTCGCTGCCCGAGTGCTCGTCTTCACTGCCCTCCTTCTCACTGCTGCTGCC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA chr19:39386201..39386575;chr19:39386253..39386500 26863196 MeRIP-seq:(Medium) rs769715236 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 111700 RMVar_ID_111700 Human_SNP_ID_833454571 m1A Human chr19 - 48875894 48875894 48875894 ACGAGCGGGAAGGTGTGGCCACAGCTTGGCTCAAGGGCGTGGTCTGGACTGGGGACGAAGGGACA ACGAGCGGGAAGGTGTGGCCACAGCTTGGCTCCAGGGCGTGGTCTGGACTGGGGACGAAGGGACA T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:48875810..48875964 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 111701 RMVar_ID_111701 Human_SNP_ID_833454835 m1A Human chr19 - 55661191 55661191 55661191 AAGGGAGAGGGTAGGGGGCAGGGGAGGGCAGTACCTCAGTGATGCCAAAGGGGATGTTGCCCACG AAGGGAGAGGGTAGGGGGCAGGGGAGGGCAGTGCCTCAGTGATGCCAAAGGGGATGTTGCCCACG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55661182..55661404 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 111702 RMVar_ID_111702 Human_SNP_ID_833466622 m1A Human chr19 + 3544612 3544611 3544613 GCTGGGTGAGGATGGAGGGTGGGGGTCCAGAGAAGAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG GCTGGGTGAGGATGGAGGGTGGGGGTCCAGAG__GAGTGAGGGGCAGTGGGGGCTTTTCCCCAAG GAA G AC005786.3 Ensembl:ENSG00000267436 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3544598..3544755 26863196 MeRIP-seq:(Medium) rs143698298 Functional Loss DEL ICGC 33..34 33 ESCA 1 - 111703 RMVar_ID_111703 Human_SNP_ID_833468438 m1A Human chr19 - 8320860 8320860 8320860 GAAGCTGCAGCTACGCTACCAGGAGATCTCCAAGCGGTGAGCAGGCCCCGCTCGCTGCCCAGCCT GAAGCTGCAGCTACGCTACCAGGAGATCTCCAGGCGGTGAGCAGGCCCCGCTCGCTGCCCAGCCT T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr19:8320851..8320925;chr19:8320851..8321396 26863196,26863410 MeRIP-seq:(Medium) rs780963864 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_4555538,Human_RBP_ID_9090556,Human_RBP_ID_9381848,Human_RBP_ID_19091999,Human_RBP_ID_26815184 Human_Splice_Rec_1949856,Human_Splice_Rec_1949857,Human_Splice_Rec_1949864,Human_Splice_Rec_1949865,Human_Splice_Rec_1949872,Human_Splice_Rec_1949873,Human_Splice_Rec_1949878,Human_Splice_Rec_1949879,Human_Splice_Rec_1949890,Human_Splice_Rec_1949891 111704 RMVar_ID_111704 Human_SNP_ID_833469378 m1A Human chr19 - 48165607 48165607 48165607 TGGATTTCTGTTCCAGGAGCAGCTGACAGACGAAGAAAAGTGCTGGACAGGAAGGGAGAATTCTG TGGATTTCTGTTCCAGGAGCAGCTGACAGACGTAGAAAAGTGCTGGACAGGAAGGGAGAATTCTG T A LIG1 Ensembl:ENSG00000105486 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48161401..48169709;chr19:48161327..48169750;chr19:48161401..48169639 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate Human_RBP_ID_4540303,Human_RBP_ID_13490167,Human_RBP_ID_22978135,Human_RBP_ID_27815544 Human_Splice_Rec_2025177,Human_Splice_Rec_2025231,Human_Splice_Rec_2025283,Human_Splice_Rec_2025335,Human_Splice_Rec_2025429,Human_Splice_Rec_2025481,Human_Splice_Rec_2025563,Human_Splice_Rec_2025601,Human_Splice_Rec_2025609,Human_Splice_Rec_2025618,Human_Splice_Rec_2025619,Human_Splice_Rec_2025627,Human_Splice_Rec_2025632,Human_Splice_Rec_2025633 RMVar_hsa_circ_319606,RMVar_hsa_circ_195660 111705 RMVar_ID_111705 Human_SNP_ID_833472770 m1A Human chr19 + 10871640 10871628 10871640 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GCGGCGGCGGCGGCGGCGGCG____________GCGGCGGCGGCCTGGGCCCGGGCGCAGCGGCG GGCGGCGGCGGCA G CARM1 Ensembl:ENSG00000142453 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10871591..10871789 26863196 MeRIP-seq:(Medium) rs1418288852 Functional Loss DEL ICGC 22..33 33 PRAD 1 - Human_RBP_ID_140280,Human_RBP_ID_4557219 111706 RMVar_ID_111706 Human_SNP_ID_833476373 m1A Human chr19 + 10681306 10681304 10681307 GGAGGACGGGGAGGAGAAGTCGCCCAGCAAAAAGAAGAAGAAGATTCAGAAGAAAGGTACAGGCC GGAGGACGGGGAGGAGAAGTCGCCCAGCAAA___AAGAAGAAGATTCAGAAGAAAGGTACAGGCC AAAG A ILF3 Ensembl:ENSG00000129351 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10681256..10681456 32194978 MeRIP-seq:(Medium) rs747091167 Functional Loss DEL ICGC 32..34 33 STAD 1 - Human_RBP_ID_53775,Human_RBP_ID_240133,Human_RBP_ID_825405,Human_RBP_ID_913237,Human_RBP_ID_1067468,Human_RBP_ID_1879617,Human_RBP_ID_3956264,Human_RBP_ID_8255757,Human_RBP_ID_9380455,Human_RBP_ID_18532249,Human_RBP_ID_24545426,Human_RBP_ID_26334841,Human_RBP_ID_26981698,Human_RBP_ID_27815110 Human_Splice_Rec_1955730,Human_Splice_Rec_1955731,Human_Splice_Rec_1955768,Human_Splice_Rec_1955806,Human_Splice_Rec_1955807,Human_Splice_Rec_1955840,Human_Splice_Rec_1955841,Human_Splice_Rec_1955926,Human_Splice_Rec_1955927,Human_Splice_Rec_1955958,Human_Splice_Rec_1955959,Human_Splice_Rec_1955988,Human_Splice_Rec_1955989,Human_Splice_Rec_1956024,Human_Splice_Rec_1956025,Human_Splice_Rec_1956056,Human_Splice_Rec_1956068,Human_Splice_Rec_1956080,Human_Splice_Rec_1956081,Human_Splice_Rec_1956092,Human_Splice_Rec_1956098 Human_miRNA_ID_2005838,Human_miRNA_ID_2005839 RMVar_hsa_circ_362795,RMVar_hsa_circ_50296,RMVar_hsa_circ_23678,RMVar_hsa_circ_92401,RMVar_hsa_circ_192412,RMVar_hsa_circ_93559,RMVar_hsa_circ_192414,RMVar_hsa_circ_100977,RMVar_hsa_circ_192416,RMVar_hsa_circ_192415 111707 RMVar_ID_111707 Human_SNP_ID_833476917 m1A Human chr19 + 55456485 55456485 55456485 GGACTCGGCCCAGGCTGGGCCTGGCAGCCGCCATTTTCTGGGGGTGGGCAGAGGGACGGTGGGTC GGACTCGGCCCAGGCTGGGCCTGGCAGCCGCCTTTTTCTGGGGGTGGGCAGAGGGACGGTGGGTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55456385..55456543 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 111708 RMVar_ID_111708 Human_SNP_ID_833479290 m1A Human chr19 - 55675257 55675257 55675257 GCCCAGAAGGGGCGCGGAGAGCCGGGCGGGGGAGGGGAGCCGCCGAGGAGACGGGAAGCAACAGA GCCCAGAAGGGGCGCGGAGAGCCGGGCGGGGGGGGGGAGCCGCCGAGGAGACGGGAAGCAACAGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:55675201..55675450 26863196 MeRIP-seq:(Medium) rs891767498 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111709 RMVar_ID_111709 Human_SNP_ID_833479529 m1A Human chr19 - 3762746 3762746 3762746 AGTGGCGGGGTTTAGGAGCTCCCAGGCCCCCCAGCCGGCCCACGTCCGGGTAGCCCCGAAAAGGC AGTGGCGGGGTTTAGGAGCTCCCAGGCCCCCCCGCCGGCCCACGTCCGGGTAGCCCCGAAAAGGC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:3762701..3762807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111710 RMVar_ID_111710 Human_SNP_ID_833480757 m1A Human chr19 - 16132985 16132985 16132985 TGATGCTCGATGGGGACCGCAGACGGGCCTGCAGACCTAACCCCTGGCTGTGGACAGGAGAGGCT TGATGCTCGATGGGGACCGCAGACGGGCCTGCGGACCTAACCCCTGGCTGTGGACAGGAGAGGCT T C AC008894.2 Ensembl:ENSG00000269243 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:16132936..16133036 32194978 MeRIP-seq:(Medium) rs17722795 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111711 RMVar_ID_111711 Human_SNP_ID_833481636 m1A Human chr19 - 47741081 47741081 47741081 GAGCCCTCCTCGCCGTCCTCCATGGCCTCGTCAGGTCCCCGCTCCACAAACGGGCCCATGTGGGT GAGCCCTCCTCGCCGTCCTCCATGGCCTCGTCGGGTCCCCGCTCCACAAACGGGCCCATGTGGGT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:47741031..47741160 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 111712 RMVar_ID_111712 Human_SNP_ID_833484674 m1A Human chr19 + 40610241 40610241 40610241 CAACCAATCTCCTGACCGCGACCCCGATTCCAACCCTGCCACACCAGAGCCCTATCCCCAAACTG CAACCAATCTCCTGACCGCGACCCCGATTCCACCCCTGCCACACCAGAGCCCTATCCCCAAACTG A C LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40610203..40610515 26863196 MeRIP-seq:(Medium) rs899257195 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_17082477 111713 RMVar_ID_111713 Human_SNP_ID_833485216 m1A Human chr19 + 1085579 1085579 1085579 CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCATCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC CCATCTCTCTCCCCCCTCTCCTGTCTCTCCCCCTCTCTCCTGTCTGTCCCTCCCCTTGTCTCTCC A C ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1085430..1085668 26863196 MeRIP-seq:(Medium) rs1489039298 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_20433160 RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 111714 RMVar_ID_111714 Human_SNP_ID_833486524 m1A Human chr19 - 18919296 18919296 18919296 CCCGGCCTCCGGCGGCTCCGGGGAGGTAGACGAGCTGTTCGACGTAAAGAACGCCTTCTACATCG CCCGGCCTCCGGCGGCTCCGGGGAGGTAGACGGGCTGTTCGACGTAAAGAACGCCTTCTACATCG T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr19:18919201..18919397;chr19:18919273..18919356 26863410 MeRIP-seq:(Medium) rs555628077 Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_1556634,Human_RBP_ID_4511404,Human_RBP_ID_5145719,Human_RBP_ID_5320292,Human_RBP_ID_5499132,Human_RBP_ID_9329939,Human_RBP_ID_22448566,Human_RBP_ID_23787136,Human_RBP_ID_26985735 Human_Splice_Rec_1981385,Human_Splice_Rec_1981403,Human_Splice_Rec_1981425,Human_Splice_Rec_1981459,Human_Splice_Rec_1981475,Human_Splice_Rec_1981489,Human_Splice_Rec_1981493 RMVar_hsa_circ_193546,RMVar_hsa_circ_86189 111715 RMVar_ID_111715 Human_SNP_ID_833486634 m1A Human chr19 + 54106010 54106010 54106010 ATGATCAACAAGGCCACGCCCTACAACTACCCAGGTGAGTGGGGGCCAGGCAGGGATCCCCGGAA ATGATCAACAAGGCCACGCCCTACAACTACCCCGGTGAGTGGGGGCCAGGCAGGGATCCCCGGAA A C NDUFA3 Ensembl:ENSG00000170906 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:54105976..54106025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 8 brain Human_RBP_ID_772037,Human_RBP_ID_914268,Human_RBP_ID_1018012,Human_RBP_ID_17271964,Human_RBP_ID_17656354,Human_RBP_ID_23114827,Human_RBP_ID_26816303 Human_Splice_Rec_2041860,Human_Splice_Rec_2041861,Human_Splice_Rec_2041868,Human_Splice_Rec_2041869,Human_Splice_Rec_2041876,Human_Splice_Rec_2041877,Human_Splice_Rec_2041884,Human_Splice_Rec_2041890,Human_Splice_Rec_2041891,Human_Splice_Rec_2041896,Human_Splice_Rec_2041897,Human_Splice_Rec_2041902,Human_Splice_Rec_2041903,Human_Splice_Rec_2041908,Human_Splice_Rec_2041909,Human_Splice_Rec_2041912,Human_Splice_Rec_2041913,Human_Splice_Rec_2041918,Human_Splice_Rec_2041919,Human_Splice_Rec_2041922,Human_Splice_Rec_2041923,Human_Splice_Rec_2041929 RMVar_hsa_circ_120853,RMVar_hsa_circ_196219 111716 RMVar_ID_111716 Human_SNP_ID_833487035 m1A Human chr19 + 49624258 49624258 49624258 GGGGTAGGTGGTTAGGATGGGGCCGAGCATTCAGGGATAGGTGGTTAGGATGGGGCTGAGAATTC GGGGTAGGTGGTTAGGATGGGGCCGAGCATTCTGGGATAGGTGGTTAGGATGGGGCTGAGAATTC A T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49623970..49624621 26863196 MeRIP-seq:(Medium) rs1264776323 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_290998 111717 RMVar_ID_111717 Human_SNP_ID_833490985 m1A Human chr19 + 2273095 2273093 2273096 GGCCTACACGTTCGAGAGAGAGTCTTCGGGAGAGGAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC GGCCTACACGTTCGAGAGAGAGTCTTCGGGA___GAGGAGGAGTAGGGCCGCCTCGGGGCTGGGC AGAG A AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:2273026..2273250 26863196 MeRIP-seq:(Medium) rs367654384 Functional Loss DEL ICGC 32..34 33 CHOL 1 - Human_RBP_ID_53041,Human_RBP_ID_239518,Human_RBP_ID_517842,Human_RBP_ID_1557688,Human_RBP_ID_1881976,Human_RBP_ID_3565770,Human_RBP_ID_4514093,Human_RBP_ID_5499203,Human_RBP_ID_6732081,Human_RBP_ID_8481367,Human_RBP_ID_8831019,Human_RBP_ID_13413348,Human_RBP_ID_17655771,Human_RBP_ID_22533274,Human_RBP_ID_22968209,Human_RBP_ID_23130877,Human_RBP_ID_23175383,Human_RBP_ID_23788966,Human_RBP_ID_27271421 RMVar_hsa_circ_123026,RMVar_hsa_circ_191248,RMVar_hsa_circ_120771,RMVar_hsa_circ_85488,RMVar_hsa_circ_191249,RMVar_hsa_circ_102385,RMVar_hsa_circ_191252,RMVar_hsa_circ_191253 111718 RMVar_ID_111718 Human_SNP_ID_833491044 m1A Human chr19 + 10148969 10148969 10148969 GTAGTCTTGATCATACCACAGCTGGTAGAAGTAGGTCTTCCCGTCGTCCCCCTCCAGCAGGGACT GTAGTCTTGATCATACCACAGCTGGTAGAAGTGGGTCTTCCCGTCGTCCCCCTCCAGCAGGGACT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10146351..10151840 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 111719 RMVar_ID_111719 Human_SNP_ID_833492381 m1A Human chr19 - 41332228 41332228 41332228 CGTGCGGCAGCTGTACATTGACTTCCGCAAGGACCTCGGCTGGAAGTGGATCCACGAGCCCAAGG CGTGCGGCAGCTGTACATTGACTTCCGCAAGGGCCTCGGCTGGAAGTGGATCCACGAGCCCAAGG T C TGFB1 Ensembl:ENSG00000105329 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:41332179..41332308 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_53248,Human_RBP_ID_1566318,Human_RBP_ID_8840095,Human_RBP_ID_9330081,Human_RBP_ID_18997903,Human_RBP_ID_21892270,Human_RBP_ID_23210971,Human_RBP_ID_26815905 Human_Splice_Rec_2011094,Human_Splice_Rec_2011108,Human_Splice_Rec_2011114 Human_miRNA_ID_2975042,Human_miRNA_ID_3008239 RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 111720 RMVar_ID_111720 Human_SNP_ID_833494555 m1A Human chr19 - 3979858 3979858 3979858 CCGTGGAGGCCAAGAACCCGGCTGACCTGCCCAAGCTGGTGGAGGGGCTGAAGCGGCTGGCCAAG CCGTGGAGGCCAAGAACCCGGCTGACCTGCCCTAGCTGGTGGAGGGGCTGAAGCGGCTGGCCAAG T A EEF2 Ensembl:ENSG00000167658 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:3979757..3980091;chr19:3979764..3980021 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 2 bladder,urinary tract Human_RBP_ID_54433,Human_RBP_ID_521476,Human_RBP_ID_1564637,Human_RBP_ID_1887324,Human_RBP_ID_3571523,Human_RBP_ID_4568163,Human_RBP_ID_6761001,Human_RBP_ID_8487007,Human_RBP_ID_8833740,Human_RBP_ID_9087806,Human_RBP_ID_9292171,Human_RBP_ID_13452438,Human_RBP_ID_17268967,Human_RBP_ID_18441295,Human_RBP_ID_18732153,Human_RBP_ID_20389826,Human_RBP_ID_22448169,Human_RBP_ID_22533076,Human_RBP_ID_22810731,Human_RBP_ID_23131210,Human_RBP_ID_26769763,Human_RBP_ID_26989668,Human_RBP_ID_27157605,Human_RBP_ID_27273986 Human_Splice_Rec_1938837 RMVar_hsa_circ_9801,RMVar_hsa_circ_91251,RMVar_hsa_circ_101398,RMVar_hsa_circ_113815,RMVar_hsa_circ_116544,RMVar_hsa_circ_124255,RMVar_hsa_circ_97804,RMVar_hsa_circ_94268,RMVar_hsa_circ_94828,RMVar_hsa_circ_93217,RMVar_hsa_circ_78875,RMVar_hsa_circ_109348,RMVar_hsa_circ_191429,RMVar_hsa_circ_191433,RMVar_hsa_circ_191437,RMVar_hsa_circ_191435,RMVar_hsa_circ_191436,RMVar_hsa_circ_191434,RMVar_hsa_circ_191431,RMVar_hsa_circ_191432,RMVar_hsa_circ_191430,RMVar_hsa_circ_125962,RMVar_hsa_circ_191428,RMVar_hsa_circ_296639,RMVar_hsa_circ_191447,RMVar_hsa_circ_84758,RMVar_hsa_circ_191448,RMVar_hsa_circ_191446,RMVar_hsa_circ_111532,RMVar_hsa_circ_191451,RMVar_hsa_circ_92462,RMVar_hsa_circ_191452,RMVar_hsa_circ_119387,RMVar_hsa_circ_120799,RMVar_hsa_circ_112221,RMVar_hsa_circ_191455,RMVar_hsa_circ_91044,RMVar_hsa_circ_110122,RMVar_hsa_circ_191457,RMVar_hsa_circ_191459,RMVar_hsa_circ_191460,RMVar_hsa_circ_191458,RMVar_hsa_circ_191456,RMVar_hsa_circ_100331,RMVar_hsa_circ_333123,RMVar_hsa_circ_334595,RMVar_hsa_circ_340763,RMVar_hsa_circ_123266,RMVar_hsa_circ_41563,RMVar_hsa_circ_114037,RMVar_hsa_circ_191462,RMVar_hsa_circ_191464,RMVar_hsa_circ_191463,RMVar_hsa_circ_191461,RMVar_hsa_circ_371516,RMVar_hsa_circ_191467,RMVar_hsa_circ_77228,RMVar_hsa_circ_91448,RMVar_hsa_circ_191468,RMVar_hsa_circ_191469,RMVar_hsa_circ_191466 111721 RMVar_ID_111721 Human_SNP_ID_833510062 m1A Human chr19 - 681531 681531 681531 CACCTGCGCAGCTGCCCGCGTGGCGCACGCCGATGGAGCGGCCCAGGAAGCAGGTGGCCTGGCGC CACCTGCGCAGCTGCCCGCGTGGCGCACGCCGTTGGAGCGGCCCAGGAAGCAGGTGGCCTGGCGC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:681501..681757 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111722 RMVar_ID_111722 Human_SNP_ID_833515696 m1A Human chr19 - 14136416 14136416 14136416 GGTGTCGGTGCTGAACGTGGCGGTCCTGGAGAACCCGAGCCCTTTCCACAGCCCCTTCCGGTTCG GGTGTCGGTGCTGAACGTGGCGGTCCTGGAGATCCCGAGCCCTTTCCACAGCCCCTTCCGGTTCG T A ASF1B Ensembl:ENSG00000105011 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:14136351..14136575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 5 lung Human_RBP_ID_1555330,Human_RBP_ID_4558163,Human_RBP_ID_5469574,Human_RBP_ID_5498970,Human_RBP_ID_13376328,Human_RBP_ID_17915750,Human_RBP_ID_18723210,Human_RBP_ID_23783710,Human_RBP_ID_27464037 Human_Splice_Rec_1968077,Human_Splice_Rec_1968083,Human_Splice_Rec_1968087,Human_Splice_Rec_1968093,Human_Splice_Rec_1968097 111723 RMVar_ID_111723 Human_SNP_ID_833516286 m1A Human chr19 + 47514858 47514855 47514858 CTCAGCCCGGTTCTCACCCAAAGAGGCCAGAGAAGAAGGACTGCGAGTTCTTCACTTTGCGCTCC CTCAGCCCGGTTCTCACCCAAAGAGGCCAG___AGAAGGACTGCGAGTTCTTCACTTTGCGCTCC GAGA G lnc-BICRA-4 RNACentral:URS00008B6A7E lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:47514851..47515000 32194978 MeRIP-seq:(Medium) rs760353871 Functional Loss DEL TCGA 31..33 33 COAD 2 - 111724 RMVar_ID_111724 Human_SNP_ID_833517996 m1A Human chr19 - 16528137 16528137 16528137 CGGGGCCCCGGGCCACACGACCAGATCCCACCAAACAAGCCCCCTTGGTTTGACCAGCCTCACCC CGGGGCCCCGGGCCACACGACCAGATCCCACCGAACAAGCCCCCTTGGTTTGACCAGCCTCACCC T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:16528076..16528250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_54929,Human_RBP_ID_8479102,Human_RBP_ID_17387300 Human_Splice_Rec_1973969,Human_Splice_Rec_1974001 111725 RMVar_ID_111725 Human_SNP_ID_833519646 m1A Human chr19 - 49537085 49537085 49537085 TGGTCGGCCACCCGGAAACGCCGCTCGTCCCGAGCCAGCATCTTTTTGTAGGTCTCTGCATCCTC TGGTCGGCCACCCGGAAACGCCGCTCGTCCCGGGCCAGCATCTTTTTGTAGGTCTCTGCATCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49536992..49537247 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRC 1 - 111726 RMVar_ID_111726 Human_SNP_ID_833520277 m1A Human chr19 + 11416635 11416635 11416635 GAAGGACCCACCTCAGGTTCTTGTTGAAGCTCAGATCTTGTACCGCTGTCTTCTTGATCTCTACC GAAGGACCCACCTCAGGTTCTTGTTGAAGCTCGGATCTTGTACCGCTGTCTTCTTGATCTCTACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11416602..11416752 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 111727 RMVar_ID_111727 Human_SNP_ID_833520343 m1A Human chr19 + 12940772 12940772 12940772 GCAGGGTGAGTGGAAGCCCCGGCAGATCGACAACCCAGATTACAAGGGCACTTGGATCCACCCAG GCAGGGTGAGTGGAAGCCCCGGCAGATCGACAGCCCAGATTACAAGGGCACTTGGATCCACCCAG A G CALR Ensembl:ENSG00000179218 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:12940635..12940775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1554877,Human_RBP_ID_1880266,Human_RBP_ID_3563355,Human_RBP_ID_4503164,Human_RBP_ID_5370042,Human_RBP_ID_6721323,Human_RBP_ID_8477497,Human_RBP_ID_9380605,Human_RBP_ID_13544584,Human_RBP_ID_17694630,Human_RBP_ID_18722839,Human_RBP_ID_20348957,Human_RBP_ID_22763308,Human_RBP_ID_22809299,Human_RBP_ID_22966976,Human_RBP_ID_23309260,Human_RBP_ID_26983138,Human_RBP_ID_27463677,Human_RBP_ID_27816143 Human_Splice_Rec_1964388,Human_Splice_Rec_1964408,Human_Splice_Rec_1964412 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_77416,RMVar_hsa_circ_192836,RMVar_hsa_circ_369902,RMVar_hsa_circ_106916,RMVar_hsa_circ_192839,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_88629,RMVar_hsa_circ_110485,RMVar_hsa_circ_192842,RMVar_hsa_circ_192843,RMVar_hsa_circ_331796,RMVar_hsa_circ_192844,RMVar_hsa_circ_192845,RMVar_hsa_circ_361141,RMVar_hsa_circ_64986,RMVar_hsa_circ_107375,RMVar_hsa_circ_126260,RMVar_hsa_circ_192847,RMVar_hsa_circ_103183,RMVar_hsa_circ_81328,RMVar_hsa_circ_192848,RMVar_hsa_circ_192849,RMVar_hsa_circ_95523,RMVar_hsa_circ_192851,RMVar_hsa_circ_16575,RMVar_hsa_circ_192850 111728 RMVar_ID_111728 Human_SNP_ID_833521340 m1A Human chr19 + 33373886 33373886 33373886 CGGAGTGGAGGCCGCCTGGGGGCAGGCGGGCTAGAGGAGCAGGTAAGGAGGCTGCGGCGGGCGCC CGGAGTGGAGGCCGCCTGGGGGCAGGCGGGCTTGAGGAGCAGGTAAGGAGGCTGCGGCGGGCGCC A T CEBPG Ensembl:ENSG00000153879 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:33373701..33373900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_519223,Human_RBP_ID_774034,Human_RBP_ID_4558336,Human_RBP_ID_5088817,Human_RBP_ID_6741570,Human_RBP_ID_8942206,Human_RBP_ID_17920514 Human_Splice_Rec_1990083,Human_Splice_Rec_1990085 111729 RMVar_ID_111729 Human_SNP_ID_833527333 m1A Human chr19 + 35786979 35786979 35786979 TCAGCCCCGGCCGGAGCCTGCGCCCCCATCTCATACCCCTGCTGCTGCGAGGAGCCGAGGCCCCG TCAGCCCCGGCCGGAGCCTGCGCCCCCATCTCTTACCCCTGCTGCTGCGAGGAGCCGAGGCCCCG A T ARHGAP33 Ensembl:ENSG00000004777 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35786940..35787185 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_23793687 Human_Splice_Rec_1996173,Human_Splice_Rec_1996226,Human_Splice_Rec_1996227,Human_Splice_Rec_1996299,Human_Splice_Rec_1996325 111730 RMVar_ID_111730 Human_SNP_ID_833528096 m1A Human chr19 + 45584760 45584760 45584760 ATAGCAGCTTCGCCATAGGGAACGCGCCCACCACCATCTTGGCGGTCTCACAGGGCACGCGCAAC ATAGCAGCTTCGCCATAGGGAACGCGCCCACCGCCATCTTGGCGGTCTCACAGGGCACGCGCAAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45584658..45584815 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 111731 RMVar_ID_111731 Human_SNP_ID_833529449 m1A Human chr19 + 7542066 7542066 7542066 AGCCGCTGCGTCTCCATGCCAGGGGACATCTCAGGTTTGGAGCACTGGGTCTGCGGGGAGGGCCA AGCCGCTGCGTCTCCATGCCAGGGGACATCTCGGGTTTGGAGCACTGGGTCTGCGGGGAGGGCCA A G PNPLA6 Ensembl:ENSG00000032444 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:7542051..7542075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_19089014 Human_Splice_Rec_1947186,Human_Splice_Rec_1947187,Human_Splice_Rec_1947288,Human_Splice_Rec_1947289,Human_Splice_Rec_1947354,Human_Splice_Rec_1947355,Human_Splice_Rec_1947420,Human_Splice_Rec_1947421,Human_Splice_Rec_1947502,Human_Splice_Rec_1947503,Human_Splice_Rec_1947582,Human_Splice_Rec_1947583,Human_Splice_Rec_1947592,Human_Splice_Rec_1947593 RMVar_hsa_circ_17569,RMVar_hsa_circ_110921,RMVar_hsa_circ_191992 111732 RMVar_ID_111732 Human_SNP_ID_833531098 m1A Human chr19 + 55651312 55651312 55651312 CAGAGGACCACTGCCGGATGAAGCCTGGGCCCAGGCGGATGGAGGGGGACAGCCGTGGTGGGGCT CAGAGGACCACTGCCGGATGAAGCCTGGGCCCGGGCGGATGGAGGGGGACAGCCGTGGTGGGGCT A G CCDC106 Ensembl:ENSG00000173581 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55649565..55651439 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney Human_RBP_ID_18995478 Human_Splice_Rec_2047866,Human_Splice_Rec_2047878,Human_Splice_Rec_2047890,Human_Splice_Rec_2047900,Human_Splice_Rec_2047910,Human_Splice_Rec_2047916 111733 RMVar_ID_111733 Human_SNP_ID_833534193 m1A Human chr19 + 15264694 15264694 15264694 CAGCTTGGTGGTCTTGGGCTCCGGGGGCAGCGAGGGTGGCTCGTGAATGGGGTCAATGGTGGTGG CAGCTTGGTGGTCTTGGGCTCCGGGGGCAGCGCGGGTGGCTCGTGAATGGGGTCAATGGTGGTGG A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:15264676..15264700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111734 RMVar_ID_111734 Human_SNP_ID_833534362 m1A Human chr19 - 4400368 4400368 4400368 TCCGGGCGGGAGGCTCGGCGGCGGGCGGCAGCATGTCGGTGGCGGGGCTGAAGAAGCAGTTCTAC TCCGGGCGGGAGGCTCGGCGGCGGGCGGCAGCGTGTCGGTGGCGGGGCTGAAGAAGCAGTTCTAC T C SH3GL1 Ensembl:ENSG00000141985 Protein coding start codon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:4400262..4400525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_240381,Human_RBP_ID_3956000,Human_RBP_ID_4533338,Human_RBP_ID_5321207,Human_RBP_ID_9328406,Human_RBP_ID_13466130,Human_RBP_ID_26335205,Human_RBP_ID_26471817 Human_Splice_Rec_1939933,Human_Splice_Rec_1939951,Human_Splice_Rec_1939969 RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 111735 RMVar_ID_111735 Human_SNP_ID_833535060 m1A Human chr19 + 39314963 39314963 39314963 GGCCGCGGAGCTGGTCGCCGCGCACCTCCGCCAGGCGGTTGCTGTCCAGGTGCAGGGCCCGGAGG GGCCGCGGAGCTGGTCGCCGCGCACCTCCGCCTGGCGGTTGCTGTCCAGGTGCAGGGCCCGGAGG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:39314915..39315044 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - 111736 RMVar_ID_111736 Human_SNP_ID_833535357 m1A Human chr19 - 48391412 48391412 48391412 GCTACCCGTTCAGACCAGCAGCCTCGGGGGGCACCCCCCCGCCAGCCTGCCTCCCTCCCGCTCAG GCTACCCGTTCAGACCAGCAGCCTCGGGGGGCCCCCCCCCGCCAGCCTGCCTCCCTCCCGCTCAG T G KDELR1 Ensembl:ENSG00000105438 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr19:48391238..48391575;chr19:48391251..48391575;chr19:48391321..48391542 26863410 MeRIP-seq:(Medium) rs969804610 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_241380,Human_RBP_ID_524863,Human_RBP_ID_773684,Human_RBP_ID_4558629,Human_RBP_ID_5130553,Human_RBP_ID_17271920,Human_RBP_ID_17386954,Human_RBP_ID_18947177,Human_RBP_ID_22447916,Human_RBP_ID_22533187,Human_RBP_ID_27276669 111737 RMVar_ID_111737 Human_SNP_ID_833535403 m1A Human chr19 + 4442309 4442309 4442309 AGACACGGAGGAGGAGGAAGAGGAGGAGGGCGACTGTATGATCGTGGATGTCCCGGATGCTGCGG AGACACGGAGGAGGAGGAAGAGGAGGAGGGCGCCTGTATGATCGTGGATGTCCCGGATGCTGCGG A C CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:4442210..4442745 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_18996079,Human_RBP_ID_22977989,Human_RBP_ID_23800266 Human_Splice_Rec_1940036,Human_Splice_Rec_1940037,Human_Splice_Rec_1940065 Human_miRNA_ID_2094628,Human_miRNA_ID_2711774,Human_miRNA_ID_2718694,Human_miRNA_ID_2872021 RMVar_hsa_circ_91068,RMVar_hsa_circ_87365,RMVar_hsa_circ_113152,RMVar_hsa_circ_191538,RMVar_hsa_circ_119539,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540,RMVar_hsa_circ_191541,RMVar_hsa_circ_191543 111738 RMVar_ID_111738 Human_SNP_ID_833538562 m1A Human chr19 + 11449286 11449286 11449286 GCCCATCCCCAGGTGCGCCTCCTGTGCGGGAAAGAGACCATGGTGACCAGCACCACAGAGCCCAG GCCCATCCCCAGGTGCGCCTCCTGTGCGGGAAGGAGACCATGGTGACCAGCACCACAGAGCCCAG A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11448526..11449500 32194978 MeRIP-seq:(Medium) rs369863173 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung Human_RBP_ID_913830,Human_RBP_ID_8476847,Human_RBP_ID_13365985,Human_RBP_ID_18191984,Human_RBP_ID_22447430,Human_RBP_ID_22762784 Human_Splice_Rec_1960690,Human_Splice_Rec_1960774,Human_Splice_Rec_1960816,Human_Splice_Rec_1960848,Human_Splice_Rec_1960878,Human_Splice_Rec_1960886,Human_Splice_Rec_1960894 RMVar_hsa_circ_112721,RMVar_hsa_circ_41607,RMVar_hsa_circ_370034,RMVar_hsa_circ_192599,RMVar_hsa_circ_192600 111739 RMVar_ID_111739 Human_SNP_ID_833539286 m1A Human chr19 - 15239977 15239977 15239977 AGCCCCCTCCCCGCTTATGATACATTCCCCCCAGATGTCACAGTTCCAGAGCCTGACCCACCAGT AGCCCCCTCCCCGCTTATGATACATTCCCCCCTGATGTCACAGTTCCAGAGCCTGACCCACCAGT T A BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:15239926..15240025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_54191,Human_RBP_ID_5130291,Human_RBP_ID_13378834,Human_RBP_ID_17082349,Human_RBP_ID_17266869,Human_RBP_ID_17386707,Human_RBP_ID_17502420,Human_RBP_ID_17916060,Human_RBP_ID_18723540,Human_RBP_ID_18946625,Human_RBP_ID_24375538,Human_RBP_ID_27464372 Human_Splice_Rec_1970630,Human_Splice_Rec_1970631 Human_miRNA_ID_955825,Human_miRNA_ID_2722718 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 111740 RMVar_ID_111740 Human_SNP_ID_833541243 m1A Human chr19 - 45854196 45854196 45854196 CTGAACCAGGCGGCGCTGATCACCAATGACTCAAAGATCACAGTGCTCAAACAGGTGAGGGCCCG CTGAACCAGGCGGCGCTGATCACCAATGACTCCAAGATCACAGTGCTCAAACAGGTGAGGGCCCG T G SYMPK Ensembl:ENSG00000125755 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45852352..45854287 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_826001,Human_RBP_ID_3955262,Human_RBP_ID_9381160,Human_RBP_ID_13477093,Human_RBP_ID_27815509 Human_Splice_Rec_2021052,Human_Splice_Rec_2021053,Human_Splice_Rec_2021104,Human_Splice_Rec_2021105,Human_Splice_Rec_2021152,Human_Splice_Rec_2021153,Human_Splice_Rec_2021228,Human_Splice_Rec_2021229,Human_Splice_Rec_2021268,Human_Splice_Rec_2021269,Human_Splice_Rec_2021310,Human_Splice_Rec_2021311,Human_Splice_Rec_2021344,Human_Splice_Rec_2021345,Human_Splice_Rec_2021354,Human_Splice_Rec_2021355,Human_Splice_Rec_2021366,Human_Splice_Rec_2021367,Human_Splice_Rec_2021375,Human_Splice_Rec_2021382 RMVar_hsa_circ_346786,RMVar_hsa_circ_127715,RMVar_hsa_circ_79946,RMVar_hsa_circ_195422,RMVar_hsa_circ_105011,RMVar_hsa_circ_195423,RMVar_hsa_circ_195424,RMVar_hsa_circ_76710,RMVar_hsa_circ_195425,RMVar_hsa_circ_93866,RMVar_hsa_circ_331450,RMVar_hsa_circ_195426,RMVar_hsa_circ_195433,RMVar_hsa_circ_355438,RMVar_hsa_circ_195443,RMVar_hsa_circ_12162,RMVar_hsa_circ_97712,RMVar_hsa_circ_195438,RMVar_hsa_circ_308553,RMVar_hsa_circ_344501,RMVar_hsa_circ_92093,RMVar_hsa_circ_195440,RMVar_hsa_circ_291775,RMVar_hsa_circ_195441,RMVar_hsa_circ_195442,RMVar_hsa_circ_92180,RMVar_hsa_circ_270494,RMVar_hsa_circ_314251,RMVar_hsa_circ_122025,RMVar_hsa_circ_195445,RMVar_hsa_circ_195446,RMVar_hsa_circ_195447,RMVar_hsa_circ_195444 111741 RMVar_ID_111741 Human_SNP_ID_833545245 m1A Human chr19 + 54187237 54187237 54187237 GAGTGGGCAGGCCCAGGAGGCTGAGGGCTCGGAAGAACAGGAGATAGGAGAAAGTCCAGGCCAGA GAGTGGGCAGGCCCAGGAGGCTGAGGGCTCGGGAGAACAGGAGATAGGAGAAAGTCCAGGCCAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54187120..54187300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111742 RMVar_ID_111742 Human_SNP_ID_833553925 m1A Human chr19 + 8485674 8485674 8485674 GTCCTGGCATTGACCGCCTCGGGGGTGCCGGCATGGAGCGCATGGGCGCGGGCCTGGGCCACGGC GTCCTGGCATTGACCGCCTCGGGGGTGCCGGCGTGGAGCGCATGGGCGCGGGCCTGGGCCACGGC A G HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:8483156..8485796 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_238905,Human_RBP_ID_529803,Human_RBP_ID_770397,Human_RBP_ID_907255,Human_RBP_ID_1067221,Human_RBP_ID_3954358,Human_RBP_ID_4575040,Human_RBP_ID_6794939,Human_RBP_ID_8233602,Human_RBP_ID_8839011,Human_RBP_ID_9258949,Human_RBP_ID_9353688,Human_RBP_ID_9380303,Human_RBP_ID_17131629,Human_RBP_ID_18994232,Human_RBP_ID_22069623,Human_RBP_ID_22446383,Human_RBP_ID_22504104,Human_RBP_ID_22664753,Human_RBP_ID_22742397,Human_RBP_ID_22977396,Human_RBP_ID_23131969,Human_RBP_ID_23812030,Human_RBP_ID_24374811,Human_RBP_ID_26334812 Human_Splice_Rec_1950162,Human_Splice_Rec_1950198,Human_Splice_Rec_1950224,Human_Splice_Rec_1950250,Human_Splice_Rec_1950276,Human_Splice_Rec_1950300,Human_Splice_Rec_1950360,Human_Splice_Rec_1950364,Human_Splice_Rec_1950368 Human_miRNA_ID_2897238 RMVar_hsa_circ_266612,RMVar_hsa_circ_118381,RMVar_hsa_circ_269338,RMVar_hsa_circ_192128 111743 RMVar_ID_111743 Human_SNP_ID_833561042 m1A Human chr19 - 3964732 3964729 3964732 CTGGCGGGGAGCTCTTTGACTTCCTGGCGGAGAAGGAGTCGCTGACGGAGGACGAGGCCACCCAG CTGGCGGGGAGCTCTTTGACTTCCTGGCGGAG___GAGTCGCTGACGGAGGACGAGGCCACCCAG CCTT C DAPK3 Ensembl:ENSG00000167657 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:3964626..3969822 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 UCEC 1 - Human_RBP_ID_5261522,Human_RBP_ID_5421514,Human_RBP_ID_5443082,Human_RBP_ID_5468753,Human_RBP_ID_5499540 RMVar_hsa_circ_41242,RMVar_hsa_circ_16480,RMVar_hsa_circ_191422,RMVar_hsa_circ_77341,RMVar_hsa_circ_310796,RMVar_hsa_circ_191427 111744 RMVar_ID_111744 Human_SNP_ID_833563472 m1A Human chr19 - 55655155 55655155 55655155 CCACACCTCCGCCCCGCGACCCCGGTGCCCTCACCTTGTTTATTCTCGTTGAGCTGCCGCTCGAA CCACACCTCCGCCCCGCGACCCCGGTGCCCTCGCCTTGTTTATTCTCGTTGAGCTGCCGCTCGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55654422..55655186 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 111745 RMVar_ID_111745 Human_SNP_ID_833570856 m1A Human chr19 + 41305735 41305735 41305735 CAGGGAGGTTACAGCCAGGGCTACACAGCCCCACCGCCTCCACCTCCACCACCACCTGCCTACAA CAGGGAGGTTACAGCCAGGGCTACACAGCCCCGCCGCCTCCACCTCCACCACCACCTGCCTACAA A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:41305650..41305839 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 9 large intestine Human_RBP_ID_4531140,Human_RBP_ID_6766023,Human_RBP_ID_8488436,Human_RBP_ID_17269419,Human_RBP_ID_17384386,Human_RBP_ID_22973410,Human_RBP_ID_26468449,Human_RBP_ID_27815463 Human_Splice_Rec_2010792,Human_Splice_Rec_2010820,Human_Splice_Rec_2010880,Human_Splice_Rec_2010908,Human_Splice_Rec_2010936,Human_Splice_Rec_2010942,Human_Splice_Rec_2011006,Human_Splice_Rec_2011046,Human_Splice_Rec_2011090 RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 111746 RMVar_ID_111746 Human_SNP_ID_833577454 m1A Human chr19 - 49004371 49004371 49004371 TCTTCCCCGTGCCCGGCTGGCCAGCAATAAGGACTGCCCGACCGGCAATCTTCCCTTCCCGGATC TCTTCCCCGTGCCCGGCTGGCCAGCAATAAGGTCTGCCCGACCGGCAATCTTCCCTTCCCGGATC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:49004326..49004375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 111747 RMVar_ID_111747 Human_SNP_ID_833579783 m1A Human chr19 + 29812733 29812733 29812733 GCGGGACACCATGAAGGAGGACGGCGGCGCGGAGTTCTCGGCTCGCTCCAGGAAGAGGAAGGCAA GCGGGACACCATGAAGGAGGACGGCGGCGCGGGGTTCTCGGCTCGCTCCAGGAAGAGGAAGGCAA A G CCNE1 Ensembl:ENSG00000105173 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:29811982..29812994 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 3 head and neck Human_RBP_ID_4516042,Human_RBP_ID_8831460,Human_RBP_ID_17919458,Human_RBP_ID_22978704,Human_RBP_ID_26784042,Human_RBP_ID_27816355 Human_Splice_Rec_1987748,Human_Splice_Rec_1987749,Human_Splice_Rec_1987770,Human_Splice_Rec_1987771,Human_Splice_Rec_1987781,Human_Splice_Rec_1987799,Human_Splice_Rec_1987815 111748 RMVar_ID_111748 Human_SNP_ID_833581474 m1A Human chr19 - 17276540 17276540 17276540 ACAAGGATGGTGCGGACCACATATGGCGGGGGAATCGTCTGCACGTTCTCTGTGACCGGAAGCTC ACAAGGATGGTGCGGACCACATATGGCGGGGGGATCGTCTGCACGTTCTCTGTGACCGGAAGCTC T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:17276476..17276625 32194978 MeRIP-seq:(Medium) rs751745605 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 111749 RMVar_ID_111749 Human_SNP_ID_833582031 m1A Human chr19 + 51366310 51366310 51366310 CGTAGTCGATGACCCTCTTGACAGCTACGAGCACGCGCAGCTCCGCCATCTTCCCGCCGCAGCCA CGTAGTCGATGACCCTCTTGACAGCTACGAGCCCGCGCAGCTCCGCCATCTTCCCGCCGCAGCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:51354093..51368474 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate 111750 RMVar_ID_111750 Human_SNP_ID_833584876 m1A Human chr19 - 4839177 4839177 4839177 CCGGAGGAGAAGAAGTAGGGGGAGAGGAGAGGACTCAGCGGGCCCCGTCTCTATAATGCAGCTGT CCGGAGGAGAAGAAGTAGGGGGAGAGGAGAGGGCTCAGCGGGCCCCGTCTCTATAATGCAGCTGT T C PLIN3 Ensembl:ENSG00000105355 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:4839126..4839200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_524654,Human_RBP_ID_770793,Human_RBP_ID_5116594,Human_RBP_ID_5144964,Human_RBP_ID_17656632,Human_RBP_ID_22448191 Human_miRNA_ID_2571345,Human_miRNA_ID_2710166,Human_miRNA_ID_3045082 RMVar_hsa_circ_92029,RMVar_hsa_circ_92973,RMVar_hsa_circ_100935,RMVar_hsa_circ_191600,RMVar_hsa_circ_191602,RMVar_hsa_circ_84442,RMVar_hsa_circ_191601,RMVar_hsa_circ_191599 111751 RMVar_ID_111751 Human_SNP_ID_833588491 m1A Human chr19 - 58563843 58563843 58563843 TCTGTTGGCTCCACCTCCAGCCTCCGAGACCCACCCACTTCCCTGCATTTGCTGAGACCATCATT TCTGTTGGCTCCACCTCCAGCCTCCGAGACCCGCCCACTTCCCTGCATTTGCTGAGACCATCATT T C MZF1 Ensembl:ENSG00000099326 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:58563805..58563926;chr19:58563792..58563989 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 3 breast Human_RBP_ID_17082681 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 111752 RMVar_ID_111752 Human_SNP_ID_833589118 m1A Human chr19 + 55343777 55343777 55343777 GGCTGCTGAGGGCCGGTGAGAATGACTTCAGCATCATGTACTCAACCCGCAAGCGGAGTGCTCAG GGCTGCTGAGGGCCGGTGAGAATGACTTCAGCTTCATGTACTCAACCCGCAAGCGGAGTGCTCAG A T KMT5C Ensembl:ENSG00000133247 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:55343636..55343838 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_9381402,Human_RBP_ID_27816747 Human_Splice_Rec_2047342,Human_Splice_Rec_2047343,Human_Splice_Rec_2047360,Human_Splice_Rec_2047361,Human_Splice_Rec_2047376,Human_Splice_Rec_2047377,Human_Splice_Rec_2047388,Human_Splice_Rec_2047389,Human_Splice_Rec_2047398,Human_Splice_Rec_2047402,Human_Splice_Rec_2047403,Human_Splice_Rec_2047410,Human_Splice_Rec_2047411 RMVar_hsa_circ_196319,RMVar_hsa_circ_99851,RMVar_hsa_circ_292301,RMVar_hsa_circ_196322,RMVar_hsa_circ_89617,RMVar_hsa_circ_196323 111753 RMVar_ID_111753 Human_SNP_ID_833595320 m1A Human chr19 - 18637090 18637090 18637090 GGGCCCGGGCCCGCGCCGAAAGCGCCGCCGCCACCAGCACCACCGCTGCTACCGCCGGACTCCGC GGGCCCGGGCCCGCGCCGAAAGCGCCGCCGCCCCCAGCACCACCGCTGCTACCGCCGGACTCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18637057..18637189 26863196 MeRIP-seq:(Medium) rs995387678 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary 111754 RMVar_ID_111754 Human_SNP_ID_833596851 m1A Human chr19 - 10141191 10141191 10141191 CTCTCCCAAACGATTGCAGTTCTCTCCTTTTCAGGCCTATAATGCAAAGAGCAAAAGCTTTGAAG CTCTCCCAAACGATTGCAGTTCTCTCCTTTTCGGGCCTATAATGCAAAGAGCAAAAGCTTTGAAG T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10141151..10141200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon medullary_carcinoma,large_intestine medullary_carcinoma 2 large intestine Human_RBP_ID_907274,Human_RBP_ID_1553312,Human_RBP_ID_2555295,Human_RBP_ID_3562169,Human_RBP_ID_13355822 Human_Splice_Rec_1953423,Human_Splice_Rec_1953503,Human_Splice_Rec_1953583,Human_Splice_Rec_1953661,Human_Splice_Rec_1953711,Human_Splice_Rec_1953715,Human_Splice_Rec_1953723,Human_Splice_Rec_1953729,Human_Splice_Rec_1953731 RMVar_hsa_circ_111275,RMVar_hsa_circ_100828,RMVar_hsa_circ_103673,RMVar_hsa_circ_192273,RMVar_hsa_circ_192274,RMVar_hsa_circ_192275,RMVar_hsa_circ_103648,RMVar_hsa_circ_192276,RMVar_hsa_circ_33091,RMVar_hsa_circ_85743,RMVar_hsa_circ_123671,RMVar_hsa_circ_192281,RMVar_hsa_circ_192282,RMVar_hsa_circ_192284,RMVar_hsa_circ_192283,RMVar_hsa_circ_87257,RMVar_hsa_circ_126435,RMVar_hsa_circ_118627,RMVar_hsa_circ_323366,RMVar_hsa_circ_338915,RMVar_hsa_circ_265839,RMVar_hsa_circ_102895,RMVar_hsa_circ_192287,RMVar_hsa_circ_90160,RMVar_hsa_circ_192285,RMVar_hsa_circ_192286,RMVar_hsa_circ_48102 111755 RMVar_ID_111755 Human_SNP_ID_833597550 m1A Human chr19 + 8483159 8483159 8483159 GCTAATTTTTTTTTCTTCCTGATTTCCTTAGAAATCCTAAGTAATGCACTGAAGAGAGGAGAGAT GCTAATTTTTTTTTCTTCCTGATTTCCTTAGACATCCTAAGTAATGCACTGAAGAGAGGAGAGAT A C HNRNPM Ensembl:ENSG00000099783 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8483151..8483225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_RBP_ID_54995,Human_RBP_ID_2572663,Human_RBP_ID_3956167,Human_RBP_ID_4575036,Human_RBP_ID_22661969,Human_RBP_ID_23812021,Human_RBP_ID_26335472,Human_RBP_ID_26997915 Human_Splice_Rec_1950160,Human_Splice_Rec_1950161,Human_Splice_Rec_1950196,Human_Splice_Rec_1950197,Human_Splice_Rec_1950222,Human_Splice_Rec_1950223,Human_Splice_Rec_1950248,Human_Splice_Rec_1950249,Human_Splice_Rec_1950274,Human_Splice_Rec_1950275,Human_Splice_Rec_1950298,Human_Splice_Rec_1950299,Human_Splice_Rec_1950362,Human_Splice_Rec_1950363,Human_Splice_Rec_1950367 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 111756 RMVar_ID_111756 Human_SNP_ID_833598453 m1A Human chr19 + 4352952 4352952 4352952 GGAGGAGTTGCTGATGGAAGAGGAGGAGGAGGACGTTCTGGCAGGGGTCTCAGCAGAGGACAAGA GGAGGAGTTGCTGATGGAAGAGGAGGAGGAGGGCGTTCTGGCAGGGGTCTCAGCAGAGGACAAGA A G MPND Ensembl:ENSG00000008382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:4345780..4352995 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRC 1 - Human_RBP_ID_18996060,Human_RBP_ID_22593074 Human_Splice_Rec_1939796,Human_Splice_Rec_1939797,Human_Splice_Rec_1939818,Human_Splice_Rec_1939819,Human_Splice_Rec_1939838,Human_Splice_Rec_1939839,Human_Splice_Rec_1939862,Human_Splice_Rec_1939863,Human_Splice_Rec_1939882,Human_Splice_Rec_1939883,Human_Splice_Rec_1939902,Human_Splice_Rec_1939903,Human_Splice_Rec_1939921 RMVar_hsa_circ_272821,RMVar_hsa_circ_338556,RMVar_hsa_circ_322480,RMVar_hsa_circ_191520,RMVar_hsa_circ_191521,RMVar_hsa_circ_191519 111757 RMVar_ID_111757 Human_SNP_ID_833600100 m1A Human chr19 - 49451550 49451550 49451550 CCAGGGCCATGGCGAACCCGAAGCTGCTGGGAATGGGGCTAAGCGAGGCGGAGGCGATCGGTGCT CCAGGGCCATGGCGAACCCGAAGCTGCTGGGACTGGGGCTAAGCGAGGCGGAGGCGATCGGTGCT T G PIH1D1 Ensembl:ENSG00000104872 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:49451476..49451550 32194978 MeRIP-seq:(Medium) rs2293012 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,salivary_gland mucinous_adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_22977799,Human_RBP_ID_26474267 Human_Splice_Rec_2030111,Human_Splice_Rec_2030208,Human_Splice_Rec_2030209,Human_Splice_Rec_2030241,Human_Splice_Rec_2030255,Human_Splice_Rec_2030266,Human_Splice_Rec_2030267,Human_Splice_Rec_2030278,Human_Splice_Rec_2030289,Human_Splice_Rec_2030297,Human_Splice_Rec_2030301,Human_Splice_Rec_2030306,Human_Splice_Rec_2030307 GWAS_ID_8418,GWAS_ID_8419,GWAS_ID_8420,GWAS_ID_8421,GWAS_ID_8422,GWAS_ID_8423,GWAS_ID_8424,GWAS_ID_8425,GWAS_ID_8426,GWAS_ID_8427,GWAS_ID_8428,GWAS_ID_8429,GWAS_ID_8430,GWAS_ID_8431,GWAS_ID_8432,GWAS_ID_8433,GWAS_ID_8434,GWAS_ID_8435 RMVar_hsa_circ_96360,RMVar_hsa_circ_195834,RMVar_hsa_circ_113228,RMVar_hsa_circ_195841 111758 RMVar_ID_111758 Human_SNP_ID_833602547 m1A Human chr19 + 54207341 54207341 54207341 CGGGGTGGGTGGAGAGGAAAGAGTGGTGCGGTAGCTGGGGTTAGCGTCCGTTTCTCCTCCAGTCC CGGGGTGGGTGGAGAGGAAAGAGTGGTGCGGTGGCTGGGGTTAGCGTCCGTTTCTCCTCCAGTCC A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:54207339..54207617 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_526711,Human_RBP_ID_5146437,Human_RBP_ID_17655678,Human_RBP_ID_22546318 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236,RMVar_hsa_circ_111374,RMVar_hsa_circ_87789,RMVar_hsa_circ_196231,RMVar_hsa_circ_196232 111759 RMVar_ID_111759 Human_SNP_ID_833604043 m1A Human chr19 - 1555381 1555381 1555381 GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGACGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC GATGAGCTTTAACTGCCGCCTCAGGCGTGGAGCCGGAGACCCCGCAGCCCGGCGGCGCCTCAGCC T G MEX3D Ensembl:ENSG00000181588 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:1555068..1555408 26863196 MeRIP-seq:(Medium) rs756753498 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_5144840,Human_RBP_ID_6724215,Human_RBP_ID_8197190,Human_RBP_ID_8830121,Human_RBP_ID_9425646,Human_RBP_ID_17916220,Human_RBP_ID_18191609,Human_RBP_ID_24483738 Human_miRNA_ID_1541041 RMVar_hsa_circ_108671,RMVar_hsa_circ_191093,RMVar_hsa_circ_191092 111760 RMVar_ID_111760 Human_SNP_ID_833605171 m1A Human chr19 - 18532758 18532746 18532758 CCACGCAGAGCTCTCAAAGCTGGTGAAGAAGCATGCGGCGCAGCGGAGCACGGAGACCGCCTTGT CCACGCAGAGCTCTCAAAGCTGGTGAAGAAGC____________GGAGCACGGAGACCGCCTTGT CGCTGCGCCGCAT C FKBP8 Ensembl:ENSG00000105701 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:18532634..18532822 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..44 33 COCA 1 - Human_RBP_ID_1881205,Human_RBP_ID_4564085 Human_Splice_Rec_1980470,Human_Splice_Rec_1980471,Human_Splice_Rec_1980478,Human_Splice_Rec_1980479,Human_Splice_Rec_1980494,Human_Splice_Rec_1980495,Human_Splice_Rec_1980508,Human_Splice_Rec_1980509,Human_Splice_Rec_1980522,Human_Splice_Rec_1980523,Human_Splice_Rec_1980536,Human_Splice_Rec_1980537,Human_Splice_Rec_1980542,Human_Splice_Rec_1980543,Human_Splice_Rec_1980548,Human_Splice_Rec_1980549 RMVar_hsa_circ_45679,RMVar_hsa_circ_45041 111761 RMVar_ID_111761 Human_SNP_ID_833607780 m1A Human chr19 + 3198779 3198779 3198779 TCTCCAAGCCCCACACACGGGTCACCTGCCCCAGGAACAGCCAGGCCATTCCCCTGCTCTCTATC TCTCCAAGCCCCACACACGGGTCACCTGCCCCGGGAACAGCCAGGCCATTCCCCTGCTCTCTATC A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3198775..3198936 26863196 MeRIP-seq:(Medium) rs311621 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,liver hepatocellular_carcinoma 7 liver Human_RBP_ID_22661698 GWAS_ID_9602 RMVar_hsa_circ_1690,RMVar_hsa_circ_104705,RMVar_hsa_circ_191318,RMVar_hsa_circ_326247,RMVar_hsa_circ_191315,RMVar_hsa_circ_347628,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_67085,RMVar_hsa_circ_337361,RMVar_hsa_circ_191319,RMVar_hsa_circ_372618,RMVar_hsa_circ_96669,RMVar_hsa_circ_191320,RMVar_hsa_circ_191321,RMVar_hsa_circ_191322 111762 RMVar_ID_111762 Human_SNP_ID_833608030 m1A Human chr19 - 15242985 15242985 15242985 CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCACCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT CAGCCCCCCCATCCGCCCCCAGGCCAGCAGCCCCCCCCGCCGCAGCCTGCCAAGCCTCAGCAAGT T G BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr19:15242976..15243184;chr19:15242860..15243000 26863196 MeRIP-seq:(Medium) rs930035134 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_514693,Human_RBP_ID_5130294,Human_RBP_ID_17082350,Human_RBP_ID_17271784,Human_RBP_ID_17386710,Human_RBP_ID_17502601,Human_RBP_ID_17656857,Human_RBP_ID_18945161 Human_Splice_Rec_1970629 Human_miRNA_ID_2147363,Human_miRNA_ID_2988789,Human_miRNA_ID_3022490 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 111763 RMVar_ID_111763 Human_SNP_ID_833611116 m1A Human chr19 - 2164240 2164240 2164240 CACTCACGTAGACCGGCAGCGGCCACGGGTAGACGGCGGGCTCAGCCCCCACGGGCGACTTCAGT CACTCACGTAGACCGGCAGCGGCCACGGGTAGCCGGCGGGCTCAGCCCCCACGGGCGACTTCAGT T G AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2163962..2164314 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 1 breast 111764 RMVar_ID_111764 Human_SNP_ID_833613330 m1A Human chr19 - 48162317 48162317 48162317 CATTTTTCCACCCCAAGAAAGAGGGTAAAGCAAAGAAGCCTGAGAAGGAGGCATCCAATAGCAGC CATTTTTCCACCCCAAGAAAGAGGGTAAAGCAGAGAAGCCTGAGAAGGAGGCATCCAATAGCAGC T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:48162216..48162399 26863196 MeRIP-seq:(Medium) rs773651278 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach diffuse_adenocarcinoma 5 stomach Human_RBP_ID_3955320,Human_RBP_ID_4540298,Human_RBP_ID_9381238,Human_RBP_ID_18998334,Human_RBP_ID_22974932,Human_RBP_ID_26334941,Human_RBP_ID_26992911,Human_RBP_ID_27815543 Human_Splice_Rec_2025178,Human_Splice_Rec_2025179,Human_Splice_Rec_2025232,Human_Splice_Rec_2025233,Human_Splice_Rec_2025284,Human_Splice_Rec_2025285,Human_Splice_Rec_2025430,Human_Splice_Rec_2025431,Human_Splice_Rec_2025482,Human_Splice_Rec_2025483,Human_Splice_Rec_2025564,Human_Splice_Rec_2025565,Human_Splice_Rec_2025602,Human_Splice_Rec_2025603,Human_Splice_Rec_2025610,Human_Splice_Rec_2025611,Human_Splice_Rec_2025620,Human_Splice_Rec_2025621,Human_Splice_Rec_2025628,Human_Splice_Rec_2025629,Human_Splice_Rec_2025634 RMVar_hsa_circ_95771,RMVar_hsa_circ_195640,RMVar_hsa_circ_331650,RMVar_hsa_circ_301176,RMVar_hsa_circ_319606,RMVar_hsa_circ_195660 111765 RMVar_ID_111765 Human_SNP_ID_833613631 m1A Human chr19 + 49086512 49086512 49086512 GCCACCCCTGGAGAAACTGCCACATGAAAAACACCACAATCAACCTTATTGTGGCATTGCGCCGT GCCACCCCTGGAGAAACTGCCACATGAAAAACCCCACAATCAACCTTATTGTGGCATTGCGCCGT A C SNRNP70 Ensembl:ENSG00000104852 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_1017491,Human_RBP_ID_1569532,Human_RBP_ID_1890846,Human_RBP_ID_2568584,Human_RBP_ID_3574970,Human_RBP_ID_8098045,Human_RBP_ID_9089176,Human_RBP_ID_9381274,Human_RBP_ID_17696192,Human_RBP_ID_17929218,Human_RBP_ID_27681986 Human_Splice_Rec_2028563,Human_Splice_Rec_2028595,Human_Splice_Rec_2028601,Human_Splice_Rec_2028619,Human_Splice_Rec_2028639,Human_Splice_Rec_2028657,Human_Splice_Rec_2028675,Human_Splice_Rec_2028683 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_314698,RMVar_hsa_circ_195800,RMVar_hsa_circ_195801 111766 RMVar_ID_111766 Human_SNP_ID_833613649 m1A Human chr19 + 11034974 11034974 11034974 AGGCCCGCAACCCCAAGCGGAAGCCGCGCCTCATGGAGGAGGACGAGCTCCCCTCGTGGATCATC AGGCCCGCAACCCCAAGCGGAAGCCGCGCCTCGTGGAGGAGGACGAGCTCCCCTCGTGGATCATC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11034901..11034975 26863196 MeRIP-seq:(Medium) rs1555785383 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 18 lung Human_RBP_ID_4500194,Human_RBP_ID_8839123,Human_RBP_ID_9293416 Human_Splice_Rec_1956920,Human_Splice_Rec_1956986,Human_Splice_Rec_1957054,Human_Splice_Rec_1957122,Human_Splice_Rec_1957190,Human_Splice_Rec_1957256,Human_Splice_Rec_1957320,Human_Splice_Rec_1957388,Human_Splice_Rec_1957452,Human_Splice_Rec_1957520,Human_Splice_Rec_1957590,Human_Splice_Rec_1957664,Human_Splice_Rec_1957732,Human_Splice_Rec_1957798,Human_Splice_Rec_1957864,Human_Splice_Rec_1957930,Human_Splice_Rec_1957996,Human_Splice_Rec_1958060,Human_Splice_Rec_1958170,Human_Splice_Rec_1958222,Human_Splice_Rec_1958276,Human_Splice_Rec_1958328,Human_Splice_Rec_1958378,Human_Splice_Rec_1958430,Human_Splice_Rec_1958480,Human_Splice_Rec_1958560,Human_Splice_Rec_1958610,Human_Splice_Rec_1958650,Human_Splice_Rec_1958694,Human_Splice_Rec_1958746,Human_Splice_Rec_1958796,Human_Splice_Rec_1958858,Human_Splice_Rec_1958898,Human_Splice_Rec_1958934,Human_Splice_Rec_1958978,Human_Splice_Rec_1959012,Human_Splice_Rec_1959032,Human_Splice_Rec_1959062,Human_Splice_Rec_1959084,Human_Splice_Rec_1959104,Human_Splice_Rec_1959114 Clinvar_Rec_397 RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_50691,RMVar_hsa_circ_283144,RMVar_hsa_circ_14259,RMVar_hsa_circ_74005,RMVar_hsa_circ_325575,RMVar_hsa_circ_367421,RMVar_hsa_circ_82983,RMVar_hsa_circ_192492,RMVar_hsa_circ_192491 111767 RMVar_ID_111767 Human_SNP_ID_833616952 m1A Human chr19 - 10320791 10320791 10320791 AAGCCGCCGCCCAGCTGAGGGCCCCCCAACTAACCCCCCAGCCCCTGGAGGTGGCAGCAGCAGCA AAGCCGCCGCCCAGCTGAGGGCCCCCCAACTACCCCCCCAGCCCCTGGAGGTGGCAGCAGCAGCA T G RAVER1 Ensembl:ENSG00000161847 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:10320740..10320838 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_910552,Human_RBP_ID_4498180 Human_miRNA_ID_1358086,Human_miRNA_ID_2017113,Human_miRNA_ID_2686095 RMVar_hsa_circ_38589,RMVar_hsa_circ_51169,RMVar_hsa_circ_86550,RMVar_hsa_circ_4985,RMVar_hsa_circ_192342 111768 RMVar_ID_111768 Human_SNP_ID_833621682 m1A Human chr19 - 16628069 16628069 16628069 CGGCTCCCCTCTCCGCCACCCCGCGCGCCCCCAACCCCCCGGCGCCGCGGGGAACATGCGGCTCC CGGCTCCCCTCTCCGCCACCCCGCGCGCCCCCCACCCCCCGGCGCCGCGGGGAACATGCGGCTCC T G AC008764.4,AC008764.1,MED26 Ensembl:ENSG00000268790,Ensembl:ENSG00000141979,Ensembl:ENSG00000105085 Protein coding,Protein coding,Protein coding intron,5'UTR,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972533,GSM1972534 HEK293T,ALKBH3 KO;HEPG2 cell line,total RNA Untreated chr19:16627876..16628200;chr19:16627907..16628133 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_4558191 111769 RMVar_ID_111769 Human_SNP_ID_833623862 m1A Human chr19 + 4695502 4695502 4695502 TCTCTGTGCTCGGGATGAACAGGGCCGGGGGGAGGAGGACGAGCTGGAGCCACTGCTGGGGCCGG TCTCTGTGCTCGGGATGAACAGGGCCGGGGGGGGGAGGACGAGCTGGAGCCACTGCTGGGGCCGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:4695384..4695525 26863196 MeRIP-seq:(Medium) rs1189248355 Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_lower_lobe adenocarcinoma,LUAD 5 lung 111770 RMVar_ID_111770 Human_SNP_ID_833627326 m1A Human chr19 - 7933975 7933975 7933975 GCAGGGGGTGGAGTCCGTGAAGAAGGAAATTGACGACAGCGTCCTGGGACAGACCGGGCCCTACC GCAGGGGGTGGAGTCCGTGAAGAAGGAAATTGGCGACAGCGTCCTGGGACAGACCGGGCCCTACC T C TIMM44 Ensembl:ENSG00000104980 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:7933951..7933975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_1574525,Human_RBP_ID_9380253,Human_RBP_ID_13533624,Human_RBP_ID_18742143,Human_RBP_ID_18994223,Human_RBP_ID_23811499 Human_Splice_Rec_1948918,Human_Splice_Rec_1948948,Human_Splice_Rec_1948986,Human_Splice_Rec_1949010,Human_Splice_Rec_1949026 RMVar_hsa_circ_86543,RMVar_hsa_circ_8745,RMVar_hsa_circ_192033,RMVar_hsa_circ_121957,RMVar_hsa_circ_352099,RMVar_hsa_circ_15771,RMVar_hsa_circ_19143,RMVar_hsa_circ_192040,RMVar_hsa_circ_192041,RMVar_hsa_circ_119069 111771 RMVar_ID_111771 Human_SNP_ID_833628706 m1A Human chr19 + 45093233 45093233 45093233 GCGGACGGAGGCGGCGCCTGAAGCGGCGGCGGAGCCCATGCCCCGGGACGGCGGGCGGACCCGGA GCGGACGGAGGCGGCGCCTGAAGCGGCGGCGGGGCCCATGCCCCGGGACGGCGGGCGGACCCGGA A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:45093160..45093509 26863196 MeRIP-seq:(Medium) rs1237837677 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_824422,Human_RBP_ID_4557591,Human_RBP_ID_5527045,Human_RBP_ID_18421419,Human_RBP_ID_18995105,Human_RBP_ID_23119207,Human_RBP_ID_27816522 RMVar_hsa_circ_267348 111772 RMVar_ID_111772 Human_SNP_ID_833630352 m1A Human chr19 + 15239926 15239926 15239926 CAGCCCTGCCAGTTACCTGTTTCTTAGGCTGGACGTTTTGCTGGGGTGGAGACTGGTGGGTCAGG CAGCCCTGCCAGTTACCTGTTTCTTAGGCTGGGCGTTTTGCTGGGGTGGAGACTGGTGGGTCAGG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:15239901..15239975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 111773 RMVar_ID_111773 Human_SNP_ID_833630724 m1A Human chr19 - 8512708 8512708 8512708 CAGTGACCACTGTTCTGTGCGTCCTGCAGGGAAGCAAATCCCTTGCTCCAGCCCTGGCTGCTGCC CAGTGACCACTGTTCTGTGCGTCCTGCAGGGATGCAAATCCCTTGCTCCAGCCCTGGCTGCTGCC T A ZNF414 Ensembl:ENSG00000133250 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:8512685..8514115 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - Human_RBP_ID_22545553 Human_Splice_Rec_1950414,Human_Splice_Rec_1950448,Human_Splice_Rec_1950458 RMVar_hsa_circ_314263 111774 RMVar_ID_111774 Human_SNP_ID_833634609 m1A Human chr19 + 14198610 14198610 14198610 GATCCTGACGCAAACCCCCTACCTCTACCCCCACCCCTGCCACAGGCCCTGGCAGCCCCACAGTC GATCCTGACGCAAACCCCCTACCTCTACCCCCCCCCCTGCCACAGGCCCTGGCAGCCCCACAGTC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:14198605..14198717 26863196 MeRIP-seq:(Medium) rs1040775675 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111775 RMVar_ID_111775 Human_SNP_ID_833636172 m1A Human chr19 - 50402271 50402253 50402271 CCTGTTCCAGGAGACGGCGGGCCGGGGCCACGAGGCGCGGCAGCGCCACGGTGATGCGCAGGAAC CCTGTTCCAGGAGACGGCGGGCCGGGGCCACG__________________GTGATGCGCAGGAAC CCGTGGCGCTGCCGCGCCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:50402210..50402305 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..50 33 LUSC 1 - 111776 RMVar_ID_111776 Human_SNP_ID_833642016 m1A Human chr19 - 4366974 4366974 4366974 TCTGTCCTCTAGCTGGTCAGTGAGAAGGTCGGAGGGGCCGAGGGGACCAAGCTGGATGATGACTT TCTGTCCTCTAGCTGGTCAGTGAGAAGGTCGGTGGGGCCGAGGGGACCAAGCTGGATGATGACTT T A SH3GL1 Ensembl:ENSG00000141985 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:4366868..4367052 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_908312,Human_RBP_ID_4533325,Human_RBP_ID_6767425,Human_RBP_ID_9381688,Human_RBP_ID_18470401,Human_RBP_ID_22590824,Human_RBP_ID_26471816 Human_Splice_Rec_1939934,Human_Splice_Rec_1939935,Human_Splice_Rec_1939952,Human_Splice_Rec_1939953,Human_Splice_Rec_1939970,Human_Splice_Rec_1939971,Human_Splice_Rec_1939986,Human_Splice_Rec_1939987,Human_Splice_Rec_1939996,Human_Splice_Rec_1939997,Human_Splice_Rec_1940006,Human_Splice_Rec_1940007 RMVar_hsa_circ_92594,RMVar_hsa_circ_16881,RMVar_hsa_circ_191524,RMVar_hsa_circ_191529,RMVar_hsa_circ_376080 111777 RMVar_ID_111777 Human_SNP_ID_833642709 m1A Human chr19 + 39178528 39178528 39178528 GAGCTGCTGAAGCACCCATTCCTGGCCAAGGCAGGGCCGCCTGCCAGCATCGTGCCCCTCATGCG GAGCTGCTGAAGCACCCATTCCTGGCCAAGGCGGGGCCGCCTGCCAGCATCGTGCCCCTCATGCG A G PAK4 Ensembl:ENSG00000130669 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:39178480..39178766 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_RBP_ID_1015799,Human_RBP_ID_18997741 111778 RMVar_ID_111778 Human_SNP_ID_833644524 m1A Human chr19 + 10987787 10987787 10987787 GCCGTCCCACCCGCCGCCTCGCCCGTGATGCCACCGCAGACCCAGTCCCCCGGGCAGCCGGCCCA GCCGTCCCACCCGCCGCCTCGCCCGTGATGCCCCCGCAGACCCAGTCCCCCGGGCAGCCGGCCCA A C SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:10987651..10987841 26863196 MeRIP-seq:(Medium) rs547268941 Functional Loss SNV COSMIC 33..33 33 meninges fibroblastic 18 brain Human_RBP_ID_9382001,Human_RBP_ID_18945050 Clinvar_Rec_391 RMVar_hsa_circ_53263,RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_51785 111779 RMVar_ID_111779 Human_SNP_ID_833648830 m1A Human chr19 - 16523148 16523148 16523148 GGCTTCAACGGGCAGCCCCCACACATGCGGCGACAGGGCCCACCCCACATCAACCACGATGACCC GGCTTCAACGGGCAGCCCCCACACATGCGGCGCCAGGGCCCACCCCACATCAACCACGATGACCC T G CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:16523053..16523194;chr19:16523098..16523320;chr19:16523101..16523250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_54924,Human_RBP_ID_17387298 Human_Splice_Rec_1973973,Human_Splice_Rec_1974005,Human_Splice_Rec_1974023 111780 RMVar_ID_111780 Human_SNP_ID_833650744 m1A Human chr19 - 17294751 17294751 17294751 TCAATGGCGGGGGCCCTACGGCGCTGGAGCCCAGCTTCTGCTCAATCTTCAACATGCCCACCTGC TCAATGGCGGGGGCCCTACGGCGCTGGAGCCCGGCTTCTGCTCAATCTTCAACATGCCCACCTGC T C ABHD8 Ensembl:ENSG00000127220 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17294700..17294828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_240094,Human_RBP_ID_27465031 Human_Splice_Rec_1976410,Human_Splice_Rec_1976411 RMVar_hsa_circ_78641,RMVar_hsa_circ_193301 111781 RMVar_ID_111781 Human_SNP_ID_833652374 m1A Human chr19 - 39836635 39836635 39836635 AATGGTGGATGTGATCTTTGCTGATGTGGCCCAGCCAGACCAGACCCGGATTGTGGCCCTGAATG AATGGTGGATGTGATCTTTGCTGATGTGGCCCTGCCAGACCAGACCCGGATTGTGGCCCTGAATG T A FBL Ensembl:ENSG00000105202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr19:39836509..39836695;chr19:39836551..39836714 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_521880,Human_RBP_ID_913603,Human_RBP_ID_1016102,Human_RBP_ID_1565288,Human_RBP_ID_1887704,Human_RBP_ID_3571811,Human_RBP_ID_4528409,Human_RBP_ID_6762639,Human_RBP_ID_8256130,Human_RBP_ID_8487543,Human_RBP_ID_13455245,Human_RBP_ID_17924888,Human_RBP_ID_18732723,Human_RBP_ID_18997819,Human_RBP_ID_22446747,Human_RBP_ID_22810903,Human_RBP_ID_23797409 Human_Splice_Rec_2006752,Human_Splice_Rec_2006753,Human_Splice_Rec_2006766,Human_Splice_Rec_2006767,Human_Splice_Rec_2006774,Human_Splice_Rec_2006775,Human_Splice_Rec_2006786,Human_Splice_Rec_2006787,Human_Splice_Rec_2006800,Human_Splice_Rec_2006801,Human_Splice_Rec_2006812,Human_Splice_Rec_2006813,Human_Splice_Rec_2006824 Human_miRNA_ID_2333361,Human_miRNA_ID_2966445 RMVar_hsa_circ_112647,RMVar_hsa_circ_89668,RMVar_hsa_circ_126403,RMVar_hsa_circ_114170,RMVar_hsa_circ_102556,RMVar_hsa_circ_92207,RMVar_hsa_circ_194786,RMVar_hsa_circ_194790,RMVar_hsa_circ_82483,RMVar_hsa_circ_85011,RMVar_hsa_circ_194788,RMVar_hsa_circ_194789,RMVar_hsa_circ_194787,RMVar_hsa_circ_194784,RMVar_hsa_circ_194785,RMVar_hsa_circ_125303,RMVar_hsa_circ_80056,RMVar_hsa_circ_109662,RMVar_hsa_circ_194795,RMVar_hsa_circ_194796,RMVar_hsa_circ_194794,RMVar_hsa_circ_352928,RMVar_hsa_circ_285971,RMVar_hsa_circ_194797,RMVar_hsa_circ_194798,RMVar_hsa_circ_194799 111782 RMVar_ID_111782 Human_SNP_ID_833654939 m1A Human chr19 + 49651647 49651647 49651647 TCTTCCGCCCCGGCGGCCGGGCCGCCCGGCCTACACCGGCCGCCTCGGCCACCCCCACGGCCCAG TCTTCCGCCCCGGCGGCCGGGCCGCCCGGCCTCCACCGGCCGCCTCGGCCACCCCCACGGCCCAG A C SCAF1 Ensembl:ENSG00000126461 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:49651322..49652225 26863410 MeRIP-seq:(Medium) rs7251334 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,COCA,large_intestine adenocarcinoma 8 caecum,head and neck,large intestine RMVar_hsa_circ_102120,RMVar_hsa_circ_73660,RMVar_hsa_circ_195896,RMVar_hsa_circ_23576,RMVar_hsa_circ_46958 111783 RMVar_ID_111783 Human_SNP_ID_833666880 m1A Human chr19 + 11447525 11447525 11447525 GAGGAGCAGCCGCCAGTGCCCTCGTCGCCCACAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGA GAGGAGCAGCCGCCAGTGCCCTCGTCGCCCACGGAGGAGGAGGAGGAGGAGGAGGAGGAGGAGGA A G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:11447476..11447525 26863196 MeRIP-seq:(Medium) rs1294882349 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_22762772,Human_RBP_ID_25382967 Human_Splice_Rec_1960678,Human_Splice_Rec_1960679,Human_Splice_Rec_1960762,Human_Splice_Rec_1960763,Human_Splice_Rec_1960804,Human_Splice_Rec_1960805,Human_Splice_Rec_1960836,Human_Splice_Rec_1960837,Human_Splice_Rec_1960856,Human_Splice_Rec_1960857,Human_Splice_Rec_1960860,Human_Splice_Rec_1960862,Human_Splice_Rec_1960863,Human_Splice_Rec_1960867 RMVar_hsa_circ_21009,RMVar_hsa_circ_192598,RMVar_hsa_circ_371287,RMVar_hsa_circ_59117 111784 RMVar_ID_111784 Human_SNP_ID_833670727 m1A Human chr19 + 10291551 10291551 10291551 TGCCTCCCTGGCAGCCGGTGGGCGAGAACTTCACCCTGAGCTGTAGGGTCCCCGGCGCCGGGCCC TGCCTCCCTGGCAGCCGGTGGGCGAGAACTTCCCCCTGAGCTGTAGGGTCCCCGGCGCCGGGCCC A C ICAM5 Ensembl:ENSG00000105376 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:10291501..10291600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_1954050,Human_Splice_Rec_1954070 111785 RMVar_ID_111785 Human_SNP_ID_833672542 m1A Human chr19 + 17425030 17425030 17425030 TCACCCTTCCGCGGAAAGAGCCCCCTTACTCCACCTCCCCGCCAGCCTGGGGCCACCCCCCCTCA TCACCCTTCCGCGGAAAGAGCCCCCTTACTCCCCCTCCCCGCCAGCCTGGGGCCACCCCCCCTCA A C MVB12A Ensembl:ENSG00000141971 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:17424926..17425290 26863196 MeRIP-seq:(Medium) rs776799800 Functional Loss SNV COSMIC 33..33 33 meninges atypical 3 brain Human_RBP_ID_515773,Human_RBP_ID_5116779,Human_RBP_ID_17386746,Human_RBP_ID_22446545,Human_RBP_ID_26817194 Human_Splice_Rec_1976910,Human_Splice_Rec_1976950,Human_Splice_Rec_1976998,Human_Splice_Rec_1977014,Human_Splice_Rec_1977022 Human_miRNA_ID_2147375,Human_miRNA_ID_2988801,Human_miRNA_ID_3022502 RMVar_hsa_circ_77474,RMVar_hsa_circ_110080,RMVar_hsa_circ_193320,RMVar_hsa_circ_193321 111786 RMVar_ID_111786 Human_SNP_ID_833677390 m1A Human chr19 + 36115603 36115603 36115603 CGGGGGTGTCGGCACCCACGGTGACCGTTTTCATCAGCAGCTCCCTCAACACCTTCCGCTCCGAG CGGGGGTGTCGGCACCCACGGTGACCGTTTTCTTCAGCAGCTCCCTCAACACCTTCCGCTCCGAG A T TBCB Ensembl:ENSG00000105254 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:36115501..36115625 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cerebellum astrocytoma_Grade_IV,central_nervous_system astrocytoma_Grade_IV 3 brain Human_RBP_ID_1561627,Human_RBP_ID_4522651,Human_RBP_ID_8484777,Human_RBP_ID_17921814,Human_RBP_ID_22234219,Human_RBP_ID_22448638,Human_RBP_ID_22970897,Human_RBP_ID_24484243,Human_RBP_ID_26815731 Human_Splice_Rec_1997815,Human_Splice_Rec_1997819,Human_Splice_Rec_1997829,Human_Splice_Rec_1997831,Human_Splice_Rec_1997837,Human_Splice_Rec_1997849,Human_Splice_Rec_1997859 RMVar_hsa_circ_103645,RMVar_hsa_circ_106961,RMVar_hsa_circ_194364,RMVar_hsa_circ_194365 111787 RMVar_ID_111787 Human_SNP_ID_833677624 m1A Human chr19 - 47039451 47039451 47039451 GGGGCCGGGGGCAACGTGTGCCCGAGGGCCACAAGGCCCAGGGCGTGGGCCCGAAGGCGCCCAGT GGGGCCGGGGGCAACGTGTGCCCGAGGGCCACGAGGCCCAGGGCGTGGGCCCGAAGGCGCCCAGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:47039064..47040544 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 111788 RMVar_ID_111788 Human_SNP_ID_833681208 m1A Human chr19 - 19182160 19182160 19182160 GGGCAGACGGAGTTCCATGTGGGGCAGTGGTGAGGGCAGACGCTCTGGGGCTGGGATCCCTGGGA GGGCAGACGGAGTTCCATGTGGGGCAGTGGTGGGGGCAGACGCTCTGGGGCTGGGATCCCTGGGA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:19182109..19182223 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_516760,Human_RBP_ID_6727623 RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596,RMVar_hsa_circ_193598,RMVar_hsa_circ_363578,RMVar_hsa_circ_367960,RMVar_hsa_circ_126091 111789 RMVar_ID_111789 Human_SNP_ID_833681845 m1A Human chr19 - 46610289 46610289 46610289 AGGTGGGCGAGGGAAGAGGCAGGGAAGAGGGCACGGAGCACAGATGTGAGGAAGCGGCGCCAAGT AGGTGGGCGAGGGAAGAGGCAGGGAAGAGGGCTCGGAGCACAGATGTGAGGAAGCGGCGCCAAGT T A AC093503.2 Ensembl:ENSG00000269292 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr19:46610126..46610400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 111790 RMVar_ID_111790 Human_SNP_ID_833685287 m1A Human chr19 - 14566239 14566239 14566239 CCCCAGCTATGTGATGCGCATGAAGGAGTTTGAGCGGGAGCGGAGGCTGCTCCAGCGGAAGAAGC CCCCAGCTATGTGATGCGCATGAAGGAGTTTGGGCGGGAGCGGAGGCTGCTCCAGCGGAAGAAGC T C NDUFB7 Ensembl:ENSG00000099795 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr19:14566131..14566308;chr19:14566151..14566300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_514452,Human_RBP_ID_1555604,Human_RBP_ID_1880586,Human_RBP_ID_3563740,Human_RBP_ID_5116138,Human_RBP_ID_17655993,Human_RBP_ID_17935270,Human_RBP_ID_18723470,Human_RBP_ID_23784071,Human_RBP_ID_26817147 Human_Splice_Rec_1969318,Human_Splice_Rec_1969322 Human_miRNA_ID_2517692 RMVar_hsa_circ_81357,RMVar_hsa_circ_193049 111791 RMVar_ID_111791 Human_SNP_ID_833687633 m1A Human chr19 - 18568405 18568405 18568405 CATCCTCTTCCTCCAGGAAGGATGCCTCTGGGATATCTGGGGGAAGGAGGCCCAAGAGTTGGTTT CATCCTCTTCCTCCAGGAAGGATGCCTCTGGGCTATCTGGGGGAAGGAGGCCCAAGAGTTGGTTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:18568401..18568500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 16 brain 111792 RMVar_ID_111792 Human_SNP_ID_833688030 m1A Human chr19 + 53089787 53089787 53089787 TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTACATATCTCATCCTCACCTTCCCTCCCTGGCTC TCCTTCCTGTGTGTTTCCCTCTCTCATTCTGTGCATATCTCATCCTCACCTTCCCTCCCTGGCTC A G NONHSAG026435.2 RNACentral:URS00008B32DF lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:53089738..53089910 26863196 MeRIP-seq:(Medium) rs7258975 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 8 brain 111793 RMVar_ID_111793 Human_SNP_ID_833689881 m1A Human chr19 + 29608655 29608655 29608655 AAGAATTGATCATTTCTTTTTTTTAATCCCCCAGGTGTGATCTACCATGCATTGTCTCAGAAAGA AAGAATTGATCATTTCTTTTTTTTAATCCCCCGGGTGTGATCTACCATGCATTGTCTCAGAAAGA A G POP4 Ensembl:ENSG00000105171 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:29608651..29608725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_22968784 Human_Splice_Rec_1987603,Human_Splice_Rec_1987615,Human_Splice_Rec_1987623,Human_Splice_Rec_1987635,Human_Splice_Rec_1987645,Human_Splice_Rec_1987655,Human_Splice_Rec_1987667,Human_Splice_Rec_1987671,Human_Splice_Rec_1987679 111794 RMVar_ID_111794 Human_SNP_ID_833697165 m1A Human chr19 - 334474 334474 334474 TCGCAGAGATCCTGTCACAGAACTACAGTGTTAGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA TCGCAGAGATCCTGTCACAGAACTACAGTGTTCGGGGGGAGTGCGAGGAGGCCTCGAGGTGCCCA T G MIER2 Ensembl:ENSG00000105556 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:334382..336172 26863196 MeRIP-seq:(Medium) rs11084956 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_4517652,Human_RBP_ID_18995527 Human_Splice_Rec_1928138,Human_Splice_Rec_1928139,Human_Splice_Rec_1928168,Human_Splice_Rec_1928169,Human_Splice_Rec_1928178,Human_Splice_Rec_1928179,Human_Splice_Rec_1928184,Human_Splice_Rec_1928185,Human_Splice_Rec_1928192,Human_Splice_Rec_1928193,Human_Splice_Rec_1928198 GWAS_ID_9595,GWAS_ID_9596,GWAS_ID_9597 RMVar_hsa_circ_104451,RMVar_hsa_circ_127778,RMVar_hsa_circ_94170,RMVar_hsa_circ_190834,RMVar_hsa_circ_190835,RMVar_hsa_circ_190836,RMVar_hsa_circ_111371,RMVar_hsa_circ_373631,RMVar_hsa_circ_190837,RMVar_hsa_circ_190838,RMVar_hsa_circ_44489,RMVar_hsa_circ_120898,RMVar_hsa_circ_371510,RMVar_hsa_circ_377053,RMVar_hsa_circ_81506,RMVar_hsa_circ_190842,RMVar_hsa_circ_190843,RMVar_hsa_circ_289245,RMVar_hsa_circ_315872,RMVar_hsa_circ_190847,RMVar_hsa_circ_190848,RMVar_hsa_circ_190849,RMVar_hsa_circ_100751,RMVar_hsa_circ_116672,RMVar_hsa_circ_340859,RMVar_hsa_circ_190850,RMVar_hsa_circ_190851,RMVar_hsa_circ_270394 111795 RMVar_ID_111795 Human_SNP_ID_833698478 m1A Human chr19 - 38837476 38837476 38837476 CTTTACTTTTCCCCTTGGTTTGCAATCAGGTGAGCGCAGCTCCTCTGGACTGCTGGAGTGGGAAT CTTTACTTTTCCCCTTGGTTTGCAATCAGGTGGGCGCAGCTCCTCTGGACTGCTGGAGTGGGAAT T C AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:38837471..38837571 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_911323,Human_RBP_ID_1564212,Human_RBP_ID_1887104,Human_RBP_ID_6759980,Human_RBP_ID_8840018,Human_RBP_ID_22662639,Human_RBP_ID_22762951,Human_RBP_ID_22977916,Human_RBP_ID_26815814 Human_Splice_Rec_2003958,Human_Splice_Rec_2003959,Human_Splice_Rec_2003968,Human_Splice_Rec_2003969,Human_Splice_Rec_2003988,Human_Splice_Rec_2003989,Human_Splice_Rec_2004010,Human_Splice_Rec_2004011,Human_Splice_Rec_2004018,Human_Splice_Rec_2004019,Human_Splice_Rec_2004040,Human_Splice_Rec_2004041,Human_Splice_Rec_2004064,Human_Splice_Rec_2004065,Human_Splice_Rec_2004076,Human_Splice_Rec_2004077,Human_Splice_Rec_2004086,Human_Splice_Rec_2004087,Human_Splice_Rec_2004108,Human_Splice_Rec_2004109 Human_miRNA_ID_2293017,Human_miRNA_ID_2358366,Human_miRNA_ID_2657757,Human_miRNA_ID_2826100,Human_miRNA_ID_2860073,Human_miRNA_ID_3060804 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_100731,RMVar_hsa_circ_117473,RMVar_hsa_circ_194675,RMVar_hsa_circ_194677,RMVar_hsa_circ_69090,RMVar_hsa_circ_194676 111796 RMVar_ID_111796 Human_SNP_ID_833699625 m1A Human chr19 - 58554145 58554145 58554145 GGAGCTACTGCGGCAGAACCAGAGGGCCCTGAACCGTGCCATGCGGGAGCTGGACCGCGAGCGAC GGAGCTACTGCGGCAGAACCAGAGGGCCCTGAGCCGTGCCATGCGGGAGCTGGACCGCGAGCGAC T C CHMP2A Ensembl:ENSG00000130724 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:58554026..58554250 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney Human_RBP_ID_1573905,Human_RBP_ID_4558844,Human_RBP_ID_9381476,Human_RBP_ID_13527515,Human_RBP_ID_22449696,Human_RBP_ID_23114787,Human_RBP_ID_27815705 Human_Splice_Rec_2052324,Human_Splice_Rec_2052334,Human_Splice_Rec_2052344,Human_Splice_Rec_2052350,Human_Splice_Rec_2052354,Human_Splice_Rec_2052356 Human_miRNA_ID_2134660,Human_miRNA_ID_2354464 RMVar_hsa_circ_101179,RMVar_hsa_circ_196576,RMVar_hsa_circ_79905,RMVar_hsa_circ_196575,RMVar_hsa_circ_89704,RMVar_hsa_circ_196577 111797 RMVar_ID_111797 Human_SNP_ID_833700781 m1A Human chr19 - 624790 624790 624790 CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCACCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG CTGTTCTGAAGGCCGTGCACAAGGTGAAGCCCGCCTTCAGCCTCCCGCCGCAGCTGCCGCCCCCG T C POLRMT Ensembl:ENSG00000099821 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:624788..624875 26863196 MeRIP-seq:(Medium) rs770914181 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_9293089,Human_RBP_ID_9327915,Human_RBP_ID_22533048 Human_Splice_Rec_1928621,Human_Splice_Rec_1928685,Human_Splice_Rec_1928695 RMVar_hsa_circ_190870,RMVar_hsa_circ_82052,RMVar_hsa_circ_116116,RMVar_hsa_circ_87843,RMVar_hsa_circ_85833,RMVar_hsa_circ_190871,RMVar_hsa_circ_6215,RMVar_hsa_circ_190868,RMVar_hsa_circ_190869,RMVar_hsa_circ_123486,RMVar_hsa_circ_87880,RMVar_hsa_circ_190885,RMVar_hsa_circ_190886,RMVar_hsa_circ_54408 111798 RMVar_ID_111798 Human_SNP_ID_833704134 m1A Human chr19 - 4361596 4361596 4361596 TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCACCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC TGGAGGTGCTTGTGCCCCTGCCGCAGTGACTCCCCCGTGTCCCCGCCCCGCCCCTCCGTCCACAC T G SH3GL1 Ensembl:ENSG00000141985 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4361226..4361812;chr19:4361426..4362622 26863196 MeRIP-seq:(Medium) rs552613793 Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 3 stomach Human_RBP_ID_240380,Human_RBP_ID_522932,Human_RBP_ID_17387166,Human_RBP_ID_22069530 Human_miRNA_ID_2147318,Human_miRNA_ID_2387343,Human_miRNA_ID_2388816,Human_miRNA_ID_2988744,Human_miRNA_ID_3022444,Human_miRNA_ID_3066344 RMVar_hsa_circ_92594,RMVar_hsa_circ_106560,RMVar_hsa_circ_99436,RMVar_hsa_circ_191525,RMVar_hsa_circ_191527,RMVar_hsa_circ_78251,RMVar_hsa_circ_191526,RMVar_hsa_circ_191524 111799 RMVar_ID_111799 Human_SNP_ID_833706662 m1A Human chr19 + 40601556 40601556 40601556 TCCATGGGCCGACCGGCTCCCGCTGTACCCCGACCTGCGCGCCCCGCAACGCCACCAGCGTGGAC TCCATGGGCCGACCGGCTCCCGCTGTACCCCGGCCTGCGCGCCCCGCAACGCCACCAGCGTGGAC A G LTBP4 Ensembl:ENSG00000090006 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:40601431..40601637 26863196 MeRIP-seq:(Medium) rs1049456552 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4560220 Human_Splice_Rec_2009183 RMVar_hsa_circ_116068,RMVar_hsa_circ_194894 111800 RMVar_ID_111800 Human_SNP_ID_833708280 m1A Human chr19 + 40214110 40214110 40214110 AGAGCTTCAAGAAGGACCCCCGCCAGTCGCTCACGCCCACCCACGTCACGGCTGCATGCGCTGTG AGAGCTTCAAGAAGGACCCCCGCCAGTCGCTCGCGCCCACCCACGTCACGGCTGCATGCGCTGTG A G MAP3K10 Ensembl:ENSG00000130758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:40214062..40214204 26863196 MeRIP-seq:(Medium) rs1338533135 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1373407,Human_RBP_ID_17925260 RMVar_hsa_circ_127469,RMVar_hsa_circ_194832,RMVar_hsa_circ_125234,RMVar_hsa_circ_194831 111801 RMVar_ID_111801 Human_SNP_ID_833708778 m1A Human chr19 - 3366615 3366594 3366615 GACGAATACATCCCGGGCGCGGCGGGAGGCGCAGGGCCGGCCGGAGCGGGCGCGCTGAACTTACT GACGAATACATCCCGGGCGCGGCGGGAGGCGC_____________________GCTGAACTTACT CGCGCCCGCTCCGGCCGGCCCT C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:3366601..3366788 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..53 33 BLCA 1 - 111802 RMVar_ID_111802 Human_SNP_ID_833710811 m1A Human chr19 + 49595559 49595559 49595559 GCAGCTGCCGGGGGTGCCACCAGGCCCCCCCCACCCCGTTCGACCGCCACCCCCAAATGTCAGAG GCAGCTGCCGGGGGTGCCACCAGGCCCCCCCCCCCCCGTTCGACCGCCACCCCCAAATGTCAGAG A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49595509..49595601 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111803 RMVar_ID_111803 Human_SNP_ID_833711735 m1A Human chr19 + 52215785 52215785 52215785 CTCCCCCTCCTCCTTCCTGTCTGCAGCTCCAGAAAGCAGTGGGGCCTGAGATCACCAAGACAGAC CTCCCCCTCCTCCTTCCTGTCTGCAGCTCCAGCAAGCAGTGGGGCCTGAGATCACCAAGACAGAC A C PPP2R1A Ensembl:ENSG00000105568 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_911925,Human_RBP_ID_8840218,Human_RBP_ID_9293924,Human_RBP_ID_22448997 Human_Splice_Rec_2039252,Human_Splice_Rec_2039268,Human_Splice_Rec_2039306,Human_Splice_Rec_2039338,Human_Splice_Rec_2039340 RMVar_hsa_circ_25465,RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_88534,RMVar_hsa_circ_196082,RMVar_hsa_circ_127662,RMVar_hsa_circ_76603,RMVar_hsa_circ_126392,RMVar_hsa_circ_127544,RMVar_hsa_circ_127787,RMVar_hsa_circ_97176,RMVar_hsa_circ_81161,RMVar_hsa_circ_196085,RMVar_hsa_circ_196087,RMVar_hsa_circ_196089,RMVar_hsa_circ_196088,RMVar_hsa_circ_196086,RMVar_hsa_circ_369728,RMVar_hsa_circ_196084,RMVar_hsa_circ_372981,RMVar_hsa_circ_122127,RMVar_hsa_circ_196091,RMVar_hsa_circ_196092,RMVar_hsa_circ_196093,RMVar_hsa_circ_122250,RMVar_hsa_circ_196094,RMVar_hsa_circ_196097,RMVar_hsa_circ_196096,RMVar_hsa_circ_78728,RMVar_hsa_circ_196095,RMVar_hsa_circ_196099,RMVar_hsa_circ_315901,RMVar_hsa_circ_322193,RMVar_hsa_circ_196098,RMVar_hsa_circ_196100,RMVar_hsa_circ_196102,RMVar_hsa_circ_299965,RMVar_hsa_circ_309744,RMVar_hsa_circ_279840,RMVar_hsa_circ_196101 111804 RMVar_ID_111804 Human_SNP_ID_833713833 m1A Human chr19 + 47745662 47745662 47745662 GGCTGCGGCCCACTTCGGTGGACCCAGCGCTGAGGCGGCGGCGGCGAGGCCCAAGAAATAAGAAG GGCTGCGGCCCACTTCGGTGGACCCAGCGCTGCGGCGGCGGCGGCGAGGCCCAAGAAATAAGAAG A C NOP53 Ensembl:ENSG00000105373 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:47745551..47745825 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney Human_RBP_ID_55126,Human_RBP_ID_524579,Human_RBP_ID_4571310,Human_RBP_ID_22974836 RMVar_hsa_circ_195620,RMVar_hsa_circ_378403 111805 RMVar_ID_111805 Human_SNP_ID_833713943 m1A Human chr19 - 12875709 12875709 12875709 GGTCACATAGCAAGACTCTGTTTCAAAAAAAAAGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT GGTCACATAGCAAGACTCTGTTTCAAAAAAAAGGGGGGGGCGGGGGACGGGTGGGTGCAGTGGCT T C DNASE2 Ensembl:ENSG00000105612 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs537971974 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_5145671,Human_RBP_ID_8198599,Human_RBP_ID_17386683,Human_RBP_ID_26472078 Human_miRNA_ID_1967484 RMVar_hsa_circ_82172,RMVar_hsa_circ_192813 111806 RMVar_ID_111806 Human_SNP_ID_833715419 m1A Human chr19 - 35629579 35629579 35629579 CTTCTACTGTGGGGACCGTGGGGACAGTGGGCACCGCAGGCACAGCAGTTGGGATTCCAGGTACT CTTCTACTGTGGGGACCGTGGGGACAGTGGGCGCCGCAGGCACAGCAGTTGGGATTCCAGGTACT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:35629501..35629660 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111807 RMVar_ID_111807 Human_SNP_ID_833715789 m1A Human chr19 + 42300190 42300190 42300190 AAGCCCCGCTCACCTTGGGCCGGATGTGTTCCAGCTCCCCATTCTCCAGCCGCCACAGTACATGC AAGCCCCGCTCACCTTGGGCCGGATGTGTTCCGGCTCCCCATTCTCCAGCCGCCACAGTACATGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:42299925..42300225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 111808 RMVar_ID_111808 Human_SNP_ID_833717354 m1A Human chr19 + 48170291 48170291 48170291 GCCGCTGCCCGGGCAACACACTCAGATCCGCCAGGCGCGCCTCTGCAGTCCCAAGTTCGCGCCAC GCCGCTGCCCGGGCAACACACTCAGATCCGCCCGGCGCGCCTCTGCAGTCCCAAGTTCGCGCCAC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:48170183..48170350;chr19:48169972..48170350;chr19:48169965..48170350;chr19:48170060..48170350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 111809 RMVar_ID_111809 Human_SNP_ID_833719572 m1A Human chr19 - 18561978 18561978 18561978 CTGCACTAGTCACCAGGTGAGGTGGGACCAAGAGGCCAGGCCGGGACCGCCATGTGCTGGAACCT CTGCACTAGTCACCAGGTGAGGTGGGACCAAGTGGCCAGGCCGGGACCGCCATGTGCTGGAACCT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:18561972..18562082 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111810 RMVar_ID_111810 Human_SNP_ID_833719896 m1A Human chr19 + 11447575 11447573 11447576 GGAGGAGGAGGAGGAAGAAGAGGCTGAAGAAGAGGAGGAGGAGGAGGATTCCGAGGTGCAGGGGG GGAGGAGGAGGAGGAAGAAGAGGCTGAAGAA___GAGGAGGAGGAGGATTCCGAGGTGCAGGGGG AGAG A PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:11447526..11447600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 COAD 1 - Human_RBP_ID_240182,Human_RBP_ID_771515,Human_RBP_ID_825097,Human_RBP_ID_912569,Human_RBP_ID_3954517,Human_RBP_ID_4500905,Human_RBP_ID_6718716,Human_RBP_ID_18470510,Human_RBP_ID_22447423,Human_RBP_ID_22762773,Human_RBP_ID_24545577,Human_RBP_ID_26335754 Human_Splice_Rec_1960679,Human_Splice_Rec_1960763,Human_Splice_Rec_1960805,Human_Splice_Rec_1960837,Human_Splice_Rec_1960857,Human_Splice_Rec_1960863,Human_Splice_Rec_1960867 RMVar_hsa_circ_21009,RMVar_hsa_circ_192598,RMVar_hsa_circ_371287,RMVar_hsa_circ_59117 111811 RMVar_ID_111811 Human_SNP_ID_833729280 m1A Human chr19 + 10996375 10996375 10996375 AGGTCGCCAAGGAGAAAAAGAAGAAAAAGAAAAAGAAGGTGTGCTGGGCCTGGCATGGTGCCCGC AGGTCGCCAAGGAGAAAAAGAAGAAAAAGAAATAGAAGGTGTGCTGGGCCTGGCATGGTGCCCGC A T SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:10996162..11007950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 18 lung Human_RBP_ID_18412493,Human_RBP_ID_24545573 Human_Splice_Rec_1956883,Human_Splice_Rec_1956951,Human_Splice_Rec_1957017,Human_Splice_Rec_1957087,Human_Splice_Rec_1957155,Human_Splice_Rec_1957221,Human_Splice_Rec_1957285,Human_Splice_Rec_1957353,Human_Splice_Rec_1957417,Human_Splice_Rec_1957485,Human_Splice_Rec_1957553,Human_Splice_Rec_1957629,Human_Splice_Rec_1957697,Human_Splice_Rec_1957763,Human_Splice_Rec_1957829,Human_Splice_Rec_1957895,Human_Splice_Rec_1957961,Human_Splice_Rec_1958023,Human_Splice_Rec_1958091,Human_Splice_Rec_1958133,Human_Splice_Rec_1958187,Human_Splice_Rec_1958241,Human_Splice_Rec_1958291,Human_Splice_Rec_1958341,Human_Splice_Rec_1958393,Human_Splice_Rec_1958443,Human_Splice_Rec_1958497,Human_Splice_Rec_1958525,Human_Splice_Rec_1958573,Human_Splice_Rec_1958613,Human_Splice_Rec_1958659,Human_Splice_Rec_1958709,Human_Splice_Rec_1958759 RMVar_hsa_circ_39568,RMVar_hsa_circ_366290,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_21716,RMVar_hsa_circ_66121,RMVar_hsa_circ_7395,RMVar_hsa_circ_51785,RMVar_hsa_circ_80212,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192481,RMVar_hsa_circ_304210,RMVar_hsa_circ_20169,RMVar_hsa_circ_192482 111812 RMVar_ID_111812 Human_SNP_ID_833729645 m1A Human chr19 - 41958850 41958850 41958850 CATCCGGCCCTGGAGCACCTTCGTGGACCAGCAGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC CATCCGGCCCTGGAGCACCTTCGTGGACCAGCGGCGCTTCTCACGGCCCCGCAACCTGGGAGAGC T C RABAC1,AC010616.1 Ensembl:ENSG00000105404,Ensembl:ENSG00000285505 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr19:41958801..41958989;chr19:41958801..41958990 26863196 MeRIP-seq:(Medium) rs112970995 Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 3 breast Human_RBP_ID_137626,Human_RBP_ID_522641,Human_RBP_ID_1566407,Human_RBP_ID_8488705,Human_RBP_ID_9088231,Human_RBP_ID_22447786 Human_Splice_Rec_2012678,Human_Splice_Rec_2012686,Human_Splice_Rec_2012692,Human_Splice_Rec_2012706,Human_Splice_Rec_2012718,Human_Splice_Rec_2012766 Human_miRNA_ID_3066403 RMVar_hsa_circ_195046,RMVar_hsa_circ_118102,RMVar_hsa_circ_97143,RMVar_hsa_circ_195050,RMVar_hsa_circ_103642,RMVar_hsa_circ_195052 111813 RMVar_ID_111813 Human_SNP_ID_833729924 m1A Human chr19 + 55096747 55096747 55096747 TCCTTCCCCGCGCAGTTCACCACCGTCTTCACACCTTCCCCGCAGTTCACCACCGTCTTCGCCCC TCCTTCCCCGCGCAGTTCACCACCGTCTTCACCCCTTCCCCGCAGTTCACCACCGTCTTCGCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55096673..55096783 26863196 MeRIP-seq:(Medium) rs942738046 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 111814 RMVar_ID_111814 Human_SNP_ID_833731757 m1A Human chr19 - 49908967 49908967 49908967 CAACATCCACCGCTGCCACCGCCACCGCCACCACCACCAGCAGCAGCAGCACCACCGGCTTTGCC CAACATCCACCGCTGCCACCGCCACCGCCACCGCCACCAGCAGCAGCAGCACCACCGGCTTTGCC T C IL4I1,NUP62 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:49908918..49909320 26863196 MeRIP-seq:(Medium) rs140091070 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_17387489,Human_RBP_ID_22068144,Human_RBP_ID_26475134 Human_miRNA_ID_272474 111815 RMVar_ID_111815 Human_SNP_ID_833732857 m1A Human chr19 + 1089493 1089493 1089493 GGCCGTCTCACCTGTCAGGCGGTAGCTACTGCACCAGCCGGTAGGTGATGTACCTGCCAGCCGTC GGCCGTCTCACCTGTCAGGCGGTAGCTACTGCCCCAGCCGGTAGGTGATGTACCTGCCAGCCGTC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:1088216..1091000 32194978 MeRIP-seq:(Medium) rs753834886 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,thyroid neoplasm,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 13 head and neck,large intestine 111816 RMVar_ID_111816 Human_SNP_ID_833734026 m1A Human chr19 - 808450 808450 808450 CTCCACCCCGGGGCCGCCCCGGCCTCTTACCCAGCTGGGCCTGGTTGCCGTCCGCCATCTGCACT CTCCACCCCGGGGCCGCCCCGGCCTCTTACCCGGCTGGGCCTGGTTGCCGTCCGCCATCTGCACT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:808432..808764 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 111817 RMVar_ID_111817 Human_SNP_ID_833735023 m1A Human chr19 - 18571911 18571911 18571911 GCAGCCCCCAACCCGCTCTCGGCCCGGCGCGAACCCGCACGACCGCCGCCACCAACCAGCTCGGC GCAGCCCCCAACCCGCTCTCGGCCCGGCGCGACCCCGCACGACCGCCGCCACCAACCAGCTCGGC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr19:18571826..18572076;chr19:18571876..18571977 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111818 RMVar_ID_111818 Human_SNP_ID_833741231 m1A Human chr19 + 40608339 40608339 40608339 AGCCACCCCGAGTGTCACTCAGCCAGCCTCGTACCCTGCCAGCCACCTCTCGGCCATCTGCAGGT AGCCACCCCGAGTGTCACTCAGCCAGCCTCGTTCCCTGCCAGCCACCTCTCGGCCATCTGCAGGT A T LTBP4 Ensembl:ENSG00000090006 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40608217..40608396 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_3955072,Human_RBP_ID_22533171 Human_Splice_Rec_2009049,Human_Splice_Rec_2009123,Human_Splice_Rec_2009197,Human_Splice_Rec_2009245 RMVar_hsa_circ_311235,RMVar_hsa_circ_194895 111819 RMVar_ID_111819 Human_SNP_ID_833743587 m1A Human chr19 + 41305750 41305750 41305750 CAGGGCTACACAGCCCCACCGCCTCCACCTCCACCACCACCTGCCTACAACTATGGGAGCTACGG CAGGGCTACACAGCCCCACCGCCTCCACCTCCTCCACCACCTGCCTACAACTATGGGAGCTACGG A T HNRNPUL1 Ensembl:ENSG00000105323 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:41305714..41305850 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 11 large intestine Human_RBP_ID_5131253,Human_RBP_ID_6766023,Human_RBP_ID_17269420,Human_RBP_ID_17384386,Human_RBP_ID_17500392 Human_Splice_Rec_2010820,Human_Splice_Rec_2010908,Human_Splice_Rec_2010936,Human_Splice_Rec_2010942,Human_Splice_Rec_2011006,Human_Splice_Rec_2011046 Human_miRNA_ID_1016721,Human_miRNA_ID_1302993 RMVar_hsa_circ_115787,RMVar_hsa_circ_195007 111820 RMVar_ID_111820 Human_SNP_ID_833744662 m1A Human chr19 + 6416400 6416400 6416400 CTGGGCCACCTGGGCCTGGTCCAACTGGGCAGAGAGGACCCTAGAAGGAAGGAGAGTAACCAAGG CTGGGCCACCTGGGCCTGGTCCAACTGGGCAGGGAGGACCCTAGAAGGAAGGAGAGTAACCAAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:6416376..6416400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 111821 RMVar_ID_111821 Human_SNP_ID_833745445 m1A Human chr19 + 17863020 17863020 17863020 GGCCAGCAAGTGCCGCCGGCCGGCTGTCAAGCAGTTCCACGTGAGTGCCCTGGGGGACTCCCCTG GGCCAGCAAGTGCCGCCGGCCGGCTGTCAAGCTGTTCCACGTGAGTGCCCTGGGGGACTCCCCTG A T RPL18A Ensembl:ENSG00000105640 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr19:17862870..17863250;chr19:17863003..17863177 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver Human_RBP_ID_17656015,Human_RBP_ID_18192098,Human_RBP_ID_19089678 Human_Splice_Rec_1978885,Human_Splice_Rec_1978901,Human_Splice_Rec_1978911,Human_Splice_Rec_1978917 RMVar_hsa_circ_108201,RMVar_hsa_circ_102454,RMVar_hsa_circ_123110,RMVar_hsa_circ_193396,RMVar_hsa_circ_193397,RMVar_hsa_circ_98959,RMVar_hsa_circ_77733,RMVar_hsa_circ_193398,RMVar_hsa_circ_193399,RMVar_hsa_circ_126749,RMVar_hsa_circ_193401,RMVar_hsa_circ_193402 111822 RMVar_ID_111822 Human_SNP_ID_833748547 m1A Human chr19 + 4431968 4431968 4431968 CTTTCTAAACCACAAGGAGTGTGCCGACCCTGAGAACCATAAGGTCCGCCAGAAACTGAAGGCCA CTTTCTAAACCACAAGGAGTGTGCCGACCCTGTGAACCATAAGGTCCGCCAGAAACTGAAGGCCA A T CHAF1A Ensembl:ENSG00000167670 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4431951..4432000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_909198,Human_RBP_ID_3954207,Human_RBP_ID_5526777,Human_RBP_ID_9380108,Human_RBP_ID_18996075,Human_RBP_ID_23800142,Human_RBP_ID_27814922 Human_Splice_Rec_1940032,Human_Splice_Rec_1940062 RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191534,RMVar_hsa_circ_87365,RMVar_hsa_circ_191537,RMVar_hsa_circ_113152,RMVar_hsa_circ_329897,RMVar_hsa_circ_191538,RMVar_hsa_circ_119539,RMVar_hsa_circ_85230,RMVar_hsa_circ_191539,RMVar_hsa_circ_191540,RMVar_hsa_circ_279390,RMVar_hsa_circ_191541,RMVar_hsa_circ_329098,RMVar_hsa_circ_191542 111823 RMVar_ID_111823 Human_SNP_ID_833748811 m1A Human chr19 - 44213072 44213071 44213072 CCCGATGACTCAATCCTTCTTAAAAAAAAAAAAGATCTGTAAAAGTTCGGGAAGAGCTCGGTCTC CCCGATGACTCAATCCTTCTTAAAAAAAAAAA_GATCTGTAAAAGTTCGGGAAGAGCTCGGTCTC CT C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:44213069..44213186 26863196 MeRIP-seq:(Medium) rs113556930 Functional Loss DEL ICGC 33..33 33 CHOL 5 - 111824 RMVar_ID_111824 Human_SNP_ID_833752342 m1A Human chr19 - 36114834 36114834 36114834 GCGCGTCGCCATGGAGCCCGACGGGACTTACGAGCCGGGCTTCGTGGGTATTCGCTTCTGCCAGG GCGCGTCGCCATGGAGCCCGACGGGACTTACGTGCCGGGCTTCGTGGGTATTCGCTTCTGCCAGG T A POLR2I Ensembl:ENSG00000105258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:36114701..36114900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_520383,Human_RBP_ID_1561618,Human_RBP_ID_1884898,Human_RBP_ID_4522622,Human_RBP_ID_5320331,Human_RBP_ID_8832685,Human_RBP_ID_9328909,Human_RBP_ID_17695383,Human_RBP_ID_18729675,Human_RBP_ID_23793813 Human_Splice_Rec_1997757,Human_Splice_Rec_1997775,Human_Splice_Rec_1997783,Human_Splice_Rec_1997793,Human_Splice_Rec_1997801 Human_miRNA_ID_2577642 RMVar_hsa_circ_123799,RMVar_hsa_circ_194363 111825 RMVar_ID_111825 Human_SNP_ID_833752592 m1A Human chr19 + 48875770 48875759 48875771 CCCAGGCCCAGGAGGAGCTGAGCCCCTGCCTCACCCCTGCTGCCCGGGCCAGAGCCTGGGCACGC CCCAGGCCCAGGAGGAGCTGAG____________CCCTGCTGCCCGGGCCAGAGCCTGGGCACGC GCCCCTGCCTCAC G PPP1R15A Ensembl:ENSG00000087074 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:48875743..48875869 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 23..34 33 BRCA 1 - Human_RBP_ID_770228,Human_RBP_ID_5117037 RMVar_hsa_circ_89556,RMVar_hsa_circ_99949,RMVar_hsa_circ_195728,RMVar_hsa_circ_195729 111826 RMVar_ID_111826 Human_SNP_ID_833756607 m1A Human chr19 + 44813345 44813345 44813345 CAGCGCCTGGAGGTGCCCGTAGAGATGAACCCAGGTGAGCAGCGCAGGAGCGCGGCGGGACGTGG CAGCGCCTGGAGGTGCCCGTAGAGATGAACCCGGGTGAGCAGCGCAGGAGCGCGGCGGGACGTGG A G BCAM Ensembl:ENSG00000187244 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:44813334..44813420 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_18998039 Human_Splice_Rec_2017708,Human_Splice_Rec_2017709,Human_Splice_Rec_2017734,Human_Splice_Rec_2017735,Human_Splice_Rec_2017764,Human_Splice_Rec_2017765,Human_Splice_Rec_2017775 111827 RMVar_ID_111827 Human_SNP_ID_833759521 m1A Human chr19 - 11437895 11437895 11437895 TTATAGCCAGTGTTGGTGCAGTGGAAGCTGCCATTAGGACAGGCAGCCGTGCCTGTGAGGAAGAA TTATAGCCAGTGTTGGTGCAGTGGAAGCTGCCGTTAGGACAGGCAGCCGTGCCTGTGAGGAAGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:11437876..11437950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 111828 RMVar_ID_111828 Human_SNP_ID_833761262 m1A Human chr19 + 868351 868351 868351 CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGAGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC CGGGCTCAGGGGCAGCTGAGGGGTAGCTGAGGGGTAGCTGAGGGGCAGCTGGGCTCAGGGGTAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:868210..868452 26863196 MeRIP-seq:(Medium) rs981655742 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 111829 RMVar_ID_111829 Human_SNP_ID_833764645 m1A Human chr19 + 45409233 45409231 45409234 CCTTGAGCCTCAGGCAGCTCCCACATCCACCAAGAAGAAGAAGAAGAAGAAAGAGAGAGGTCACA CCTTGAGCCTCAGGCAGCTCCCACATCCACC___AAGAAGAAGAAGAAGAAAGAGAGAGGTCACA CAAG C CD3EAP Ensembl:ENSG00000117877 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:45409182..45409282 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 ESCA 1 - Human_RBP_ID_53484,Human_RBP_ID_914969,Human_RBP_ID_17936509,Human_RBP_ID_26336413 RMVar_hsa_circ_195342,RMVar_hsa_circ_112799 111830 RMVar_ID_111830 Human_SNP_ID_833764993 m1A Human chr19 - 12801071 12801071 12801071 TGGGCCCTAACTCCTCTGTGTCCCTCCTCCCCAGGGAAGTACGTGGTCCTCTTTTTCTACCCTCT TGGGCCCTAACTCCTCTGTGTCCCTCCTCCCCGGGGAAGTACGTGGTCCTCTTTTTCTACCCTCT T C PRDX2,HOOK2 Ensembl:ENSG00000167815,Ensembl:ENSG00000095066 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:12801057..12801143 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_5375807,Human_RBP_ID_22593446 RMVar_hsa_circ_115238,RMVar_hsa_circ_112810,RMVar_hsa_circ_192788,RMVar_hsa_circ_192787,RMVar_hsa_circ_331336,RMVar_hsa_circ_192794 111831 RMVar_ID_111831 Human_SNP_ID_833765114 m1A Human chr19 - 13960524 13960524 13960524 TCCTGTTGACGTAGCGGCCGCTGCTCTCCGGCACCAGCCACTTCATGACCATGTCCACGCAGCTC TCCTGTTGACGTAGCGGCCGCTGCTCTCCGGCCCCAGCCACTTCATGACCATGTCCACGCAGCTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13960476..13960575 32194978 MeRIP-seq:(Medium) rs202218518 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,THCA 2 head and neck 111832 RMVar_ID_111832 Human_SNP_ID_833765541 m1A Human chr19 - 648226 648226 648226 GCCGAAAAAGCCTCACGGGACAGAACACGGCCACGAACCCCCCTGGCCTCACTGGGGTGAGCTTC GCCGAAAAAGCCTCACGGGACAGAACACGGCCCCGAACCCCCCTGGCCTCACTGGGGTGAGCTTC T G RNF126 Ensembl:ENSG00000070423 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:648002..648990 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_Splice_Rec_1928724,Human_Splice_Rec_1928740,Human_Splice_Rec_1928756,Human_Splice_Rec_1928762,Human_Splice_Rec_1928778 111833 RMVar_ID_111833 Human_SNP_ID_833767796 m1A Human chr19 - 7910327 7910327 7910327 CGTGGCCGGTCTTCCGGAAGCGCATCTTCCACACCTGGCCGCAGGTGCCGCTGCCCATCTCGCCC CGTGGCCGGTCTTCCGGAAGCGCATCTTCCACGCCTGGCCGCAGGTGCCGCTGCCCATCTCGCCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7910276..7910375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111834 RMVar_ID_111834 Human_SNP_ID_833774907 m1A Human chr19 - 21359145 21359145 21359145 CCCTCTCTCGGGATGTTGGACCCCGCACTCTCACCATTTCTAGGCTTCCAGGGTGTCCCGGCGTC CCCTCTCTCGGGATGTTGGACCCCGCACTCTCGCCATTTCTAGGCTTCCAGGGTGTCCCGGCGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:21359107..21359215 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111835 RMVar_ID_111835 Human_SNP_ID_833775405 m1A Human chr19 - 18574919 18574919 18574919 CAGTTGTATTTCTGGGCAAGCTGGCGGAGAGAAGGCTCAATAATGCCACCTCGCAGGCGCAACAC CAGTTGTATTTCTGGGCAAGCTGGCGGAGAGACGGCTCAATAATGCCACCTCGCAGGCGCAACAC T G CRLF1 Ensembl:ENSG00000006016 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr19:18574851..18575224 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 12 large intestine 111836 RMVar_ID_111836 Human_SNP_ID_833778642 m1A Human chr19 + 49596409 49596409 49596409 GGGGACCACCGGGTACACCCTACGAGTTGGCCAAGGAAGACCCCCAGAGGTACCACCTGCAGAGT GGGGACCACCGGGTACACCCTACGAGTTGGCCCAGGAAGACCCCCAGAGGTACCACCTGCAGAGT A C PRR12 Ensembl:ENSG00000126464 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:49596358..49596450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_240081,Human_RBP_ID_826754,Human_RBP_ID_3957354,Human_RBP_ID_5527101,Human_RBP_ID_18412568,Human_RBP_ID_22068003,Human_RBP_ID_22718388,Human_RBP_ID_26336614,Human_RBP_ID_27573114 RMVar_hsa_circ_195887,RMVar_hsa_circ_115272 111837 RMVar_ID_111837 Human_SNP_ID_833790445 m1A Human chr19 + 45885152 45885151 45885153 CCCGGCCTCGCATGGCCTCGTTCAGTTCTGCCAGACAGTCCGCATTCCTCTGCTGCTTCTCTTTC CCCGGCCTCGCATGGCCTCGTTCAGTTCTGCC__ACAGTCCGCATTCCTCTGCTGCTTCTCTTTC CAG C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:45885102..45885194 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - 111838 RMVar_ID_111838 Human_SNP_ID_833794778 m1A Human chr19 - 5131283 5131283 5131283 CTAGCTCCTCACTGGGCACCTCAGGGGGCACGACATTAAGGGGTGCCGGCAGGGGGCTCTCCTCC CTAGCTCCTCACTGGGCACCTCAGGGGGCACGGCATTAAGGGGTGCCGGCAGGGGGCTCTCCTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5113326..5135450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111839 RMVar_ID_111839 Human_SNP_ID_833796853 m1A Human chr19 + 46201914 46201905 46201914 CCAGCCACCTCTCTAAGAGGAAATTGTTGGGCAGGTTGGGGAGGGCTAGTCACGGAACAAAACTG CCAGCCACCTCTCTAAGAGGAAAT_________GGTTGGGGAGGGCTAGTCACGGAACAAAACTG TTGTTGGGCA T AC006262.1 Ensembl:ENSG00000268460 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46201911..46202186 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 25..33 33 LMS 2 - 111840 RMVar_ID_111840 Human_SNP_ID_833797924 m1A Human chr19 - 4947188 4947188 4947188 TCCACAAACCTGTTGGTGTTGGTGAGTTTCTGATCACAAGACTGTTCCGCGGTCCTCTTGTTGCC TCCACAAACCTGTTGGTGTTGGTGAGTTTCTGGTCACAAGACTGTTCCGCGGTCCTCTTGTTGCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:4947176..4947200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111841 RMVar_ID_111841 Human_SNP_ID_833800380 m1A Human chr19 + 54461268 54461268 54461268 CTCTCTCTTTCGAGCTTGCACTCCGGTACCCGACCCGGCGCCCTGGCCCATCCCATGCCGGGGGG CTCTCTCTTTCGAGCTTGCACTCCGGTACCCGTCCCGGCGCCCTGGCCCATCCCATGCCGGGGGG A T LENG8 Ensembl:ENSG00000167615 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:54461226..54461375 32194978 MeRIP-seq:(Medium) rs1411576958 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_55511,Human_RBP_ID_526760,Human_RBP_ID_772771,Human_RBP_ID_1570941,Human_RBP_ID_5117113,Human_RBP_ID_5145884,Human_RBP_ID_8256339,Human_RBP_ID_13507909,Human_RBP_ID_18166458,Human_RBP_ID_18739087,Human_RBP_ID_22070546,Human_RBP_ID_22663183,Human_RBP_ID_24559722,Human_RBP_ID_25440859,Human_RBP_ID_27839656 Human_Splice_Rec_2043914 111842 RMVar_ID_111842 Human_SNP_ID_833803562 m1A Human chr19 - 43592224 43592224 43592224 CCAGGCCCGGTGACGCGCGCCGAGGTGGAAGCAAGACTGGGCGCCTGGGCGGGCGAGGGCACTGC CCAGGCCCGGTGACGCGCGCCGAGGTGGAAGCGAGACTGGGCGCCTGGGCGGGCGAGGGCACTGC T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding CDS,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:43592099..43592464 26863196 MeRIP-seq:(Medium) rs1568527358 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_773088,Human_RBP_ID_4533641,Human_RBP_ID_5088824,Human_RBP_ID_18461969 Human_miRNA_ID_1265203 111843 RMVar_ID_111843 Human_SNP_ID_833803712 m1A Human chr19 + 11394393 11394393 11394393 TGCCTGTGGGACTTGTGTCTTGTGGAGAGGACAGGGCTGCCTCAGCTTGGGGAGACAGACAGAGT TGCCTGTGGGACTTGTGTCTTGTGGAGAGGACTGGGCTGCCTCAGCTTGGGGAGACAGACAGAGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11394345..11394495 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 111844 RMVar_ID_111844 Human_SNP_ID_833807627 m1A Human chr19 + 38945340 38945340 38945340 GGTCCTGGGGAGGAGCCAGAGCCTGGGGGAGGAGCCTGGGTGGTCCTGGGGTGGAGCCAGAGCCT GGTCCTGGGGAGGAGCCAGAGCCTGGGGGAGGGGCCTGGGTGGTCCTGGGGTGGAGCCAGAGCCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:38945318..38945502 26863196 MeRIP-seq:(Medium) rs1231826466 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111845 RMVar_ID_111845 Human_SNP_ID_833808557 m1A Human chr19 - 55518188 55518188 55518188 GTGGTGGGGTAAGGGGTCGTGGTGGGGTCAGGAGTCATGGTGGGGTGAGGGGTTGTGGTGGGGTG GTGGTGGGGTAAGGGGTCGTGGTGGGGTCAGGGGTCATGGTGGGGTGAGGGGTTGTGGTGGGGTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:55518145..55518451 26863196 MeRIP-seq:(Medium) rs1472186933 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 111846 RMVar_ID_111846 Human_SNP_ID_833808901 m1A Human chr19 - 39125881 39125881 39125881 GGCGCCGCAGTCGCTCGCGGCCTAACTGCTCGACCTGGAACTCCGCGCCCTCGCGCCTCCCTCAG GGCGCCGCAGTCGCTCGCGGCCTAACTGCTCGGCCTGGAACTCCGCGCCCTCGCGCCTCCCTCAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:39125801..39125943 26863410 MeRIP-seq:(Medium) rs4803206 Functional Loss SNV ICGC 33..33 33 LAML 1 - 111847 RMVar_ID_111847 Human_SNP_ID_833814715 m1A Human chr19 - 41906790 41906790 41906790 CCCCAGGTGCCCCACTCACCTTCCTGGGCGGGAACCTCAAGTGCAGCCAGGCTGGGGGACAGAGT CCCCAGGTGCCCCACTCACCTTCCTGGGCGGGCACCTCAAGTGCAGCCAGGCTGGGGGACAGAGT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:41906742..41907394 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney 111848 RMVar_ID_111848 Human_SNP_ID_833817587 m1A Human chr19 - 38831414 38831414 38831414 GGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGACCACAGCTATGAGTCCCTTCGTGTGACGTCTG GGCTTCCGGAGTAGCCCTCGGTGAAGCCCCAGGCCACAGCTATGAGTCCCTTCGTGTGACGTCTG T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:38831363..38831512 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_770489,Human_RBP_ID_825575,Human_RBP_ID_1564173,Human_RBP_ID_1887091,Human_RBP_ID_4567855,Human_RBP_ID_8486653,Human_RBP_ID_8839344,Human_RBP_ID_18731783,Human_RBP_ID_22446719 Human_Splice_Rec_2003937 RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 111849 RMVar_ID_111849 Human_SNP_ID_833817877 m1A Human chr19 - 7916758 7916758 7916758 CGGCACCCGGGCTCGGCGGCGGCGGTGGCGGGAAGGCGACAGAGGTGTCGGCGGGGCAGCCCTCA CGGCACCCGGGCTCGGCGGCGGCGGTGGCGGGGAGGCGACAGAGGTGTCGGCGGGGCAGCCCTCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:7916339..7917761 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111850 RMVar_ID_111850 Human_SNP_ID_833820453 m1A Human chr19 - 12939628 12939628 12939628 GAGATCAGCACCAGGAAGCAGGCCCTCACCAAACATGATGTTGTATTCTGAGTCTCCGTGCATGT GAGATCAGCACCAGGAAGCAGGCCCTCACCAAGCATGATGTTGTATTCTGAGTCTCCGTGCATGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:12939398..12939657 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 stomach adenocarcinoma,UCEC,endometrium endometrioid_carcinoma 4 uterus,stomach 111851 RMVar_ID_111851 Human_SNP_ID_833821268 m1A Human chr19 + 13805041 13805041 13805041 GCTCTCCCAGATGAACCGGGACCAGCTGCAGAAGTTCGTGCAGTACCTCATCAGCGCCCATCACA GCTCTCCCAGATGAACCGGGACCAGCTGCAGACGTTCGTGCAGTACCTCATCAGCGCCCATCACA A C ZSWIM4 Ensembl:ENSG00000132003 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:13804991..13814535 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_38419,RMVar_hsa_circ_72822,RMVar_hsa_circ_192928,RMVar_hsa_circ_21621,RMVar_hsa_circ_333963,RMVar_hsa_circ_336137,RMVar_hsa_circ_192929 111852 RMVar_ID_111852 Human_SNP_ID_833822789 m1A Human chr19 - 17831327 17831327 17831327 CCTGGCCGCCCGAAACATCCTCGTGGAGAGCGAGGCACACGTCAAGATCGCTGACTTCGGCCTAG CCTGGCCGCCCGAAACATCCTCGTGGAGAGCGCGGCACACGTCAAGATCGCTGACTTCGGCCTAG T G JAK3 Ensembl:ENSG00000105639 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17831325..17831416 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia 3 haematopoietic and lymphoid tissue Human_Splice_Rec_1978746,Human_Splice_Rec_1978747,Human_Splice_Rec_1978792,Human_Splice_Rec_1978793,Human_Splice_Rec_1978838,Human_Splice_Rec_1978839 RMVar_hsa_circ_85677,RMVar_hsa_circ_266365,RMVar_hsa_circ_122321,RMVar_hsa_circ_193390,RMVar_hsa_circ_193391,RMVar_hsa_circ_58783 111853 RMVar_ID_111853 Human_SNP_ID_833823460 m1A Human chr19 + 5587725 5587725 5587725 CACCTTACCCCGCCACTCCACCGCGGCTTGCCATGTGCCCCGGCCCCGAGGGCCCAGACAGGCCC CACCTTACCCCGCCACTCCACCGCGGCTTGCCTTGTGCCCCGGCCCCGAGGGCCCAGACAGGCCC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:5587138..5588000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 111854 RMVar_ID_111854 Human_SNP_ID_833823833 m1A Human chr19 + 11025449 11025449 11025449 TCCAGGGCAAAGGCGGCACCAAGACCCTGATGAACACCATCATGCAGCTGCGGAAGATCTGCAAC TCCAGGGCAAAGGCGGCACCAAGACCCTGATGTACACCATCATGCAGCTGCGGAAGATCTGCAAC A T SMARCA4 Ensembl:ENSG00000127616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:11024353..11025475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lymph_node mantle_cell_lymphoma,haematopoietic_and_lymphoid_tissue mantle_cell_lymphoma 18 haematopoietic and lymphoid tissue Human_RBP_ID_1012901,Human_RBP_ID_1879827,Human_RBP_ID_13363970,Human_RBP_ID_17694512,Human_RBP_ID_18721957,Human_RBP_ID_26816998 Human_Splice_Rec_1956906,Human_Splice_Rec_1956907,Human_Splice_Rec_1956974,Human_Splice_Rec_1956975,Human_Splice_Rec_1957040,Human_Splice_Rec_1957041,Human_Splice_Rec_1957110,Human_Splice_Rec_1957111,Human_Splice_Rec_1957178,Human_Splice_Rec_1957179,Human_Splice_Rec_1957244,Human_Splice_Rec_1957245,Human_Splice_Rec_1957308,Human_Splice_Rec_1957309,Human_Splice_Rec_1957376,Human_Splice_Rec_1957377,Human_Splice_Rec_1957440,Human_Splice_Rec_1957441,Human_Splice_Rec_1957508,Human_Splice_Rec_1957509,Human_Splice_Rec_1957576,Human_Splice_Rec_1957577,Human_Splice_Rec_1957652,Human_Splice_Rec_1957653,Human_Splice_Rec_1957720,Human_Splice_Rec_1957721,Human_Splice_Rec_1957786,Human_Splice_Rec_1957787,Human_Splice_Rec_1957852,Human_Splice_Rec_1957853,Human_Splice_Rec_1957918,Human_Splice_Rec_1957919,Human_Splice_Rec_1957984,Human_Splice_Rec_1957985,Human_Splice_Rec_1958046,Human_Splice_Rec_1958047,Human_Splice_Rec_1958114,Human_Splice_Rec_1958115,Human_Splice_Rec_1958156,Human_Splice_Rec_1958157,Human_Splice_Rec_1958210,Human_Splice_Rec_1958211,Human_Splice_Rec_1958264,Human_Splice_Rec_1958265,Human_Splice_Rec_1958314,Human_Splice_Rec_1958315,Human_Splice_Rec_1958364,Human_Splice_Rec_1958365,Human_Splice_Rec_1958416,Human_Splice_Rec_1958417,Human_Splice_Rec_1958466,Human_Splice_Rec_1958467,Human_Splice_Rec_1958518,Human_Splice_Rec_1958519,Human_Splice_Rec_1958548,Human_Splice_Rec_1958549,Human_Splice_Rec_1958596,Human_Splice_Rec_1958597,Human_Splice_Rec_1958636,Human_Splice_Rec_1958637,Human_Splice_Rec_1958682,Human_Splice_Rec_1958683,Human_Splice_Rec_1958732,Human_Splice_Rec_1958733,Human_Splice_Rec_1958782,Human_Splice_Rec_1958783,Human_Splice_Rec_1958822,Human_Splice_Rec_1958823,Human_Splice_Rec_1958844,Human_Splice_Rec_1958845,Human_Splice_Rec_1958884,Human_Splice_Rec_1958885,Human_Splice_Rec_1958922,Human_Splice_Rec_1958923,Human_Splice_Rec_1958966,Human_Splice_Rec_1958967,Human_Splice_Rec_1958998,Human_Splice_Rec_1959020,Human_Splice_Rec_1959021,Human_Splice_Rec_1959048,Human_Splice_Rec_1959049 RMVar_hsa_circ_15608,RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_38789,RMVar_hsa_circ_192489,RMVar_hsa_circ_29226,RMVar_hsa_circ_50691 111855 RMVar_ID_111855 Human_SNP_ID_833831306 m1A Human chr19 + 38729392 38729392 38729392 CCCTGACGCCGTGCCCGGTGCCCTCGACTACAAGTCCTTCTCCACGGCCTTGTATGGCGAGAGCG CCCTGACGCCGTGCCCGGTGCCCTCGACTACAGGTCCTTCTCCACGGCCTTGTATGGCGAGAGCG A G ACTN4 Ensembl:ENSG00000130402 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr19:38729341..38729525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_521175,Human_RBP_ID_1189510,Human_RBP_ID_5191533,Human_RBP_ID_8486605,Human_RBP_ID_8833575,Human_RBP_ID_18193049,Human_RBP_ID_22446711,Human_RBP_ID_22810661,Human_RBP_ID_27467724 RMVar_hsa_circ_101860,RMVar_hsa_circ_89445,RMVar_hsa_circ_194658,RMVar_hsa_circ_194661 111856 RMVar_ID_111856 Human_SNP_ID_833832001 m1A Human chr19 - 35720256 35720256 35720256 ACTTTTTTGGCCCTTGAAACAAACTTGATCACAAAGGGGAGCCCACCACCTCGGCCGCGGCCCCT ACTTTTTTGGCCCTTGAAACAAACTTGATCACTAAGGGGAGCCCACCACCTCGGCCGCGGCCCCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:35719946..35720795 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 111857 RMVar_ID_111857 Human_SNP_ID_833835246 m1A Human chr19 - 45688525 45688525 45688525 CAACAAGCCCAAGAGTGAGATGACCCCAGAGGAGCTGCAGAAGCGAGAGGAGGAGGAATTTAACA CAACAAGCCCAAGAGTGAGATGACCCCAGAGGCGCTGCAGAAGCGAGAGGAGGAGGAATTTAACA T G SNRPD2 Ensembl:ENSG00000125743 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:45688426..45688600 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_240017,Human_RBP_ID_523730,Human_RBP_ID_1568342,Human_RBP_ID_1890103,Human_RBP_ID_4570472,Human_RBP_ID_8490257,Human_RBP_ID_9088811,Human_RBP_ID_9381146,Human_RBP_ID_17657210,Human_RBP_ID_26334935,Human_RBP_ID_26816027,Human_RBP_ID_26991759 Human_Splice_Rec_2020514,Human_Splice_Rec_2020524,Human_Splice_Rec_2020528,Human_Splice_Rec_2020534,Human_Splice_Rec_2020540,Human_Splice_Rec_2020544 Human_miRNA_ID_2014032,Human_miRNA_ID_2760430 RMVar_hsa_circ_121142,RMVar_hsa_circ_123868,RMVar_hsa_circ_113835,RMVar_hsa_circ_195409,RMVar_hsa_circ_195410,RMVar_hsa_circ_195408,RMVar_hsa_circ_195411,RMVar_hsa_circ_310432 111858 RMVar_ID_111858 Human_SNP_ID_833839000 m1A Human chr19 + 572688 572688 572688 CTGCTGGGATTCGCGCTGCTGGGCACCCACGGAGCCTCCGGGGCTGGTGAGGAGCGGGTAGGGGG CTGCTGGGATTCGCGCTGCTGGGCACCCACGGCGCCTCCGGGGCTGGTGAGGAGCGGGTAGGGGG A C BSG Ensembl:ENSG00000172270 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr19:572576..575104;chr19:572601..575104;chr19:572576..572725 26863410,32194978,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_240634,Human_RBP_ID_772085,Human_RBP_ID_826241,Human_RBP_ID_1572154,Human_RBP_ID_4556913,Human_RBP_ID_5144745,Human_RBP_ID_5319662,Human_RBP_ID_8494654,Human_RBP_ID_8837378,Human_RBP_ID_9327908,Human_RBP_ID_18191511,Human_RBP_ID_18740151,Human_RBP_ID_22446238,Human_RBP_ID_22764291,Human_RBP_ID_26769705 Human_Splice_Rec_1928489,Human_Splice_Rec_1928491,Human_Splice_Rec_1928499,Human_Splice_Rec_1928513,Human_Splice_Rec_1928517,Human_Splice_Rec_1928519,Human_Splice_Rec_1928529,Human_Splice_Rec_1928545,Human_Splice_Rec_1928553,Human_Splice_Rec_1928563 RMVar_hsa_circ_111780,RMVar_hsa_circ_190861 111859 RMVar_ID_111859 Human_SNP_ID_833842030 m1A Human chr19 + 10395103 10395103 10395103 GGCTCTTGGCCAGCTCCAGGATAAATTGCATGACGATTGTCTGGTGGGCCACCTGCTCCATGAGT GGCTCTTGGCCAGCTCCAGGATAAATTGCATGGCGATTGTCTGGTGGGCCACCTGCTCCATGAGT A G lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:10395001..10395224 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus 111860 RMVar_ID_111860 Human_SNP_ID_833842262 m1A Human chr19 + 15110041 15110041 15110041 ACCTCCTTCCGGCCCTACGAGGTGGGTCCCGCAGCCCGGGCACCCCCGGCCGCACTCTGGGGCCG ACCTCCTTCCGGCCCTACGAGGTGGGTCCCGCCGCCCGGGCACCCCCGGCCGCACTCTGGGGCCG A C SYDE1 Ensembl:ENSG00000105137 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:15109689..15110187 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_79995,RMVar_hsa_circ_76187,RMVar_hsa_circ_193081,RMVar_hsa_circ_193082 111861 RMVar_ID_111861 Human_SNP_ID_833844270 m1A Human chr19 - 804886 804886 804886 CACGGGGTCCGCATACTGCAGCAGGGCCTGGAACTGGTTGTTCTTGGTGAAGGTGATGATCTTCA CACGGGGTCCGCATACTGCAGCAGGGCCTGGAGCTGGTTGTTCTTGGTGAAGGTGATGATCTTCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:804876..804900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 7 haematopoietic and lymphoid tissue 111862 RMVar_ID_111862 Human_SNP_ID_833845898 m1A Human chr19 + 17721006 17721006 17721006 CTTGATGAACAGCTCAAGGTCTTTGTGTCCCGACACTCTGCCACCTTCTCCAGCATTGTGAAAGG CTTGATGAACAGCTCAAGGTCTTTGTGTCCCGGCACTCTGCCACCTTCTCCAGCATTGTGAAAGG A G MAP1S Ensembl:ENSG00000130479 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:17720941..17721305 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_8830428,Human_RBP_ID_9084977,Human_RBP_ID_9291370 Human_Splice_Rec_1977874,Human_Splice_Rec_1977875,Human_Splice_Rec_1977882,Human_Splice_Rec_1977883,Human_Splice_Rec_1977894,Human_Splice_Rec_1977895,Human_Splice_Rec_1977902,Human_Splice_Rec_1977903,Human_Splice_Rec_1977910,Human_Splice_Rec_1977911,Human_Splice_Rec_1977922,Human_Splice_Rec_1977923,Human_Splice_Rec_1977932,Human_Splice_Rec_1977933,Human_Splice_Rec_1977940,Human_Splice_Rec_1977941,Human_Splice_Rec_1977948,Human_Splice_Rec_1977949,Human_Splice_Rec_1977956,Human_Splice_Rec_1977957,Human_Splice_Rec_1977968,Human_Splice_Rec_1977969,Human_Splice_Rec_1977976,Human_Splice_Rec_1977977,Human_Splice_Rec_1977982,Human_Splice_Rec_1977983,Human_Splice_Rec_1977986,Human_Splice_Rec_1977987,Human_Splice_Rec_1977993,Human_Splice_Rec_1978000,Human_Splice_Rec_1978001 RMVar_hsa_circ_114723,RMVar_hsa_circ_370294,RMVar_hsa_circ_193371,RMVar_hsa_circ_193372 111863 RMVar_ID_111863 Human_SNP_ID_833846363 m1A Human chr19 + 16878621 16878621 16878621 CCTGGTGCAGGACTGGCTGATGGGTGAGGAGGACGAGGACATGGTACCCTGCAAGACGCTGTGTG CCTGGTGCAGGACTGGCTGATGGGTGAGGAGGTCGAGGACATGGTACCCTGCAAGACGCTGTGTG A T SIN3B Ensembl:ENSG00000127511 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:16878570..16878688 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_5526894,Human_RBP_ID_8830357 111864 RMVar_ID_111864 Human_SNP_ID_833848428 m1A Human chr19 + 48813265 48813265 48813265 CCCAGCTCTGCACCCCCCGTCACGAGCAGTTCAATGCCCGTGCAGAAGTTGGCTTCGGAGGCCAG CCCAGCTCTGCACCCCCCGTCACGAGCAGTTCGATGCCCGTGCAGAAGTTGGCTTCGGAGGCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:48813164..48836333 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 111865 RMVar_ID_111865 Human_SNP_ID_833851161 m1A Human chr19 - 2733319 2733319 2733319 CATCGACCTGGAGACCTTCAACGCCGGATCGGACGTGGGCAGCGACTCGGAGTATGAGAGCCCCT CATCGACCTGGAGACCTTCAACGCCGGATCGGCCGTGGGCAGCGACTCGGAGTATGAGAGCCCCT T G AC006538.2,SLC39A3 Ensembl:ENSG00000267001,Ensembl:ENSG00000141873 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2733268..2733425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_13417666,Human_RBP_ID_22590678,Human_RBP_ID_27466390 RMVar_hsa_circ_89042,RMVar_hsa_circ_106069,RMVar_hsa_circ_191274,RMVar_hsa_circ_191275 111866 RMVar_ID_111866 Human_SNP_ID_833853108 m1A Human chr19 - 34399322 34399322 34399322 CAAATGCAGAAGTGCTGACCTTATGTGGCAGCAGCCTCTCAAGGTCCTCTGGACTCTTGCCCGCA CAAATGCAGAAGTGCTGACCTTATGTGGCAGCGGCCTCTCAAGGTCCTCTGGACTCTTGCCCGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:34399226..34399350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 111867 RMVar_ID_111867 Human_SNP_ID_833855383 m1A Human chr19 - 17323448 17323448 17323448 TCAGTCATTCACAGGGGCGGCCGGTCTCCAAAATGCAAAATGCGCTTCAGCCCCCGAGGGCCCCC TCAGTCATTCACAGGGGCGGCCGGTCTCCAAACTGCAAAATGCGCTTCAGCCCCCGAGGGCCCCC T G ANO8 Ensembl:ENSG00000074855 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17323397..17323488 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18724275 Human_miRNA_ID_979902,Human_miRNA_ID_984630 111868 RMVar_ID_111868 Human_SNP_ID_833864768 m1A Human chr19 + 45287634 45287634 45287634 AGCGCCCACAACCCCAACAAGGCAGAGATCCCAGAGCGGCGGAAGGACAGCACGAGCACCCCCGT AGCGCCCACAACCCCAACAAGGCAGAGATCCCCGAGCGGCGGAAGGACAGCACGAGCACCCCCGT A C MARK4 Ensembl:ENSG00000007047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:45287414..45287706 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas Human_Splice_Rec_2018585,Human_Splice_Rec_2018617 RMVar_hsa_circ_93983,RMVar_hsa_circ_9377,RMVar_hsa_circ_114875,RMVar_hsa_circ_195297,RMVar_hsa_circ_88830,RMVar_hsa_circ_195308,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_195307,RMVar_hsa_circ_26071,RMVar_hsa_circ_195317,RMVar_hsa_circ_101057,RMVar_hsa_circ_304047,RMVar_hsa_circ_375992,RMVar_hsa_circ_121313,RMVar_hsa_circ_195318,RMVar_hsa_circ_195316,RMVar_hsa_circ_358665,RMVar_hsa_circ_42346 111869 RMVar_ID_111869 Human_SNP_ID_833865802 m1A Human chr19 - 281476 281476 281476 CCGACCCCCACAGCACTGTCTGAAGGAGGAGGAGCTGGAACGGAAGCCCAGCCTGTCACTGACGT CCGACCCCCACAGCACTGTCTGAAGGAGGAGGTGCTGGAACGGAAGCCCAGCCTGTCACTGACGT T A PLPP2 Ensembl:ENSG00000141934 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:281426..281550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung mixed_adenosquamous_carcinoma 3 lung Human_Splice_Rec_1928088,Human_Splice_Rec_1928098,Human_Splice_Rec_1928108,Human_Splice_Rec_1928112,Human_Splice_Rec_1928122 111870 RMVar_ID_111870 Human_SNP_ID_833867269 m1A Human chr19 - 5131135 5131135 5131135 CGGGGGCGGCAGCTGTGGGGGCAGCAGGCCGAAGCTCTTCTTCTTCCGCTCGCTCTTGGCCTTGG CGGGGGCGGCAGCTGTGGGGGCAGCAGGCCGACGCTCTTCTTCTTCCGCTCGCTCTTGGCCTTGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:5131031..5131268;chr19:5131034..5131296 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine 111871 RMVar_ID_111871 Human_SNP_ID_833868826 m1A Human chr19 + 40717170 40717170 40717170 GAGGCGCTGCCCGTGCCGTGGGAGCCTGAACGAGGCGGAGGCCGGGGCGCTGCCCGCGGCGGCCC GAGGCGCTGCCCGTGCCGTGGGAGCCTGAACGCGGCGGAGGCCGGGGCGCTGCCCGCGGCGGCCC A C ITPKC Ensembl:ENSG00000086544 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:40717052..40717318 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_121327,RMVar_hsa_circ_194911 111872 RMVar_ID_111872 Human_SNP_ID_833870275 m1A Human chr19 - 54201258 54201258 54201258 GCCACTCACCGATCAGCTTCAGCTCTTGGTCGAGACGAGATTTCTCGAAGGGTCTCCGCGGGGTC GCCACTCACCGATCAGCTTCAGCTCTTGGTCGTGACGAGATTTCTCGAAGGGTCTCCGCGGGGTC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:54201151..54201325 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 77 kidney 111873 RMVar_ID_111873 Human_SNP_ID_833870390 m1A Human chr19 - 45478617 45478617 45478617 AACCTGTAGCTGTCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGGTAGTAACTAAGCGCC AACCTGTAGCTGTCTAGCGACAGAGTGGTTCATTTCCACCTTTCGGGCGGTAGTAACTAAGCGCC T A ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs111386994 Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_7748,Human_RBP_ID_239023,Human_RBP_ID_270107,Human_RBP_ID_523637,Human_RBP_ID_1133471,Human_RBP_ID_1190640,Human_RBP_ID_1295015,Human_RBP_ID_1373764,Human_RBP_ID_1568313,Human_RBP_ID_1890082,Human_RBP_ID_2567342,Human_RBP_ID_3573811,Human_RBP_ID_4536879,Human_RBP_ID_5145298,Human_RBP_ID_5190724,Human_RBP_ID_5238821,Human_RBP_ID_5275323,Human_RBP_ID_5421647,Human_RBP_ID_5468928,Human_RBP_ID_5499779,Human_RBP_ID_5641073,Human_RBP_ID_6773587,Human_RBP_ID_8256218,Human_RBP_ID_8490195,Human_RBP_ID_8728084,Human_RBP_ID_8835465,Human_RBP_ID_9088798,Human_RBP_ID_9292466,Human_RBP_ID_9329027,Human_RBP_ID_9341102,Human_RBP_ID_13475392,Human_RBP_ID_17068374,Human_RBP_ID_17084371,Human_RBP_ID_17131947,Human_RBP_ID_17927876,Human_RBP_ID_18179875,Human_RBP_ID_18208434,Human_RBP_ID_18441635,Human_RBP_ID_18514969,Human_RBP_ID_18532560,Human_RBP_ID_18735805,Human_RBP_ID_18947483,Human_RBP_ID_20404038,Human_RBP_ID_21892296,Human_RBP_ID_21908725,Human_RBP_ID_22005467,Human_RBP_ID_22067440,Human_RBP_ID_22236292,Human_RBP_ID_22391290,Human_RBP_ID_22546138,Human_RBP_ID_22592120,Human_RBP_ID_22742533,Human_RBP_ID_22763045,Human_RBP_ID_22811245,Human_RBP_ID_23131472,Human_RBP_ID_23279446,Human_RBP_ID_23801248,Human_RBP_ID_24374707,Human_RBP_ID_24418805,Human_RBP_ID_24484510,Human_RBP_ID_24533195,Human_RBP_ID_24559934,Human_RBP_ID_26749637,Human_RBP_ID_26760159,Human_RBP_ID_26769840,Human_RBP_ID_26991727,Human_RBP_ID_27157685,Human_RBP_ID_27275701,Human_RBP_ID_27469116 RMVar_hsa_circ_122004,RMVar_hsa_circ_195351 111874 RMVar_ID_111874 Human_SNP_ID_833871088 m1A Human chr19 - 15243277 15243277 15243277 CCCACCCCTCACCTCCATGCAGATGCAGCTGTACCTGCAGCAGCTGCAGAAGGTGCAGCCCCCTA CCCACCCCTCACCTCCATGCAGATGCAGCTGTGCCTGCAGCAGCTGCAGAAGGTGCAGCCCCCTA T C BRD4 Ensembl:ENSG00000141867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:15243068..15243319 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_54194,Human_RBP_ID_514695,Human_RBP_ID_5130297,Human_RBP_ID_5320224,Human_RBP_ID_17081742,Human_RBP_ID_17656858,Human_RBP_ID_18946631,Human_RBP_ID_26335892 Human_miRNA_ID_1489732,Human_miRNA_ID_2013962,Human_miRNA_ID_2760361 RMVar_hsa_circ_116984,RMVar_hsa_circ_193122 111875 RMVar_ID_111875 Human_SNP_ID_833874144 m1A Human chr19 - 4343722 4343722 4343722 CGGCGCCTCCTCGCCCGCACCGCCCGCCGGGGACAGCGGCTCCGGAGCTGCGGACAGCGAGAGGC CGGCGCCTCCTCGCCCGCACCGCCCGCCGGGGGCAGCGGCTCCGGAGCTGCGGACAGCGAGAGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr19:4343575..4354127;chr19:4343576..4353017 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 111876 RMVar_ID_111876 Human_SNP_ID_833882205 m1A Human chr19 - 2418226 2418225 2418226 GAAGGAGGGGGGGAAGGAAAGAAAGGAAAAAAATCTAGGTCTGCACACAAAGAACTGCTGGGTGA GAAGGAGGGGGGGAAGGAAAGAAAGGAAAAAA_TCTAGGTCTGCACACAAAGAACTGCTGGGTGA AT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:2418118..2422034 26863196 MeRIP-seq:(Medium) rs984350108 Functional Loss DEL ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1188161,Human_RBP_ID_17068493,Human_RBP_ID_22978622,Human_RBP_ID_25442958 111877 RMVar_ID_111877 Human_SNP_ID_833884934 m1A Human chr19 - 40442062 40442062 40442062 CTCTACAGGGCATCATGGTGGGAGGCTTGAAGAGGAAACACTCTGATTTGGAAGAGGAGGAGGAG CTCTACAGGGCATCATGGTGGGAGGCTTGAAGTGGAAACACTCTGATTTGGAAGAGGAGGAGGAG T A SERTAD3 Ensembl:ENSG00000167565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr19:40441741..40442361;chr19:40441878..40442361;chr19:40441681..40442361 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_907772,Human_RBP_ID_8942449,Human_RBP_ID_9328941,Human_RBP_ID_19096288 Human_Splice_Rec_2008214,Human_Splice_Rec_2008218,Human_Splice_Rec_2008222 111878 RMVar_ID_111878 Human_SNP_ID_833884968 m1A Human chr19 + 48450371 48450371 48450371 GGCTGGGGTGTGGTCAGAGAAGGGCCAGGTGGAGGTGTTTGCGCTGCGGCGGCTTCTGCAGGTGG GGCTGGGGTGTGGTCAGAGAAGGGCCAGGTGGCGGTGTTTGCGCTGCGGCGGCTTCTGCAGGTGG A C GRWD1 Ensembl:ENSG00000105447 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:48450301..48450469;chr19:48450276..48450450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_55144,Human_RBP_ID_772469,Human_RBP_ID_9381248,Human_RBP_ID_18995231,Human_RBP_ID_22448899 Human_Splice_Rec_2026538,Human_Splice_Rec_2026548 RMVar_hsa_circ_348134 111879 RMVar_ID_111879 Human_SNP_ID_833885918 m1A Human chr19 - 42388711 42388711 42388711 GATACTACCTCATGCCTTCCCACACTCAACTTATCAGGCCCTCAACCTCCCCTTTGCATGCTCAG GATACTACCTCATGCCTTCCCACACTCAACTTCTCAGGCCCTCAACCTCCCCTTTGCATGCTCAG T G CNFN Ensembl:ENSG00000105427 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:42388662..42388772 26863196 MeRIP-seq:(Medium) rs12165114 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_10112,GWAS_ID_10113,GWAS_ID_10114 111880 RMVar_ID_111880 Human_SNP_ID_833892383 m1A Human chr19 + 12611007 12611007 12611007 CCCCTTGACGCGTCAGGTTGCTGTACCCCTGCATCGGATGCGCTGTACCCTGCGCTGGCTCCGTG CCCCTTGACGCGTCAGGTTGCTGTACCCCTGCGTCGGATGCGCTGTACCCTGCGCTGGCTCCGTG A G ZNF791 Ensembl:ENSG00000173875 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12610958..12611069 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - Human_RBP_ID_4501927,Human_RBP_ID_13369547,Human_RBP_ID_18420861,Human_RBP_ID_26335767 Human_Splice_Rec_1962161,Human_Splice_Rec_1962165,Human_Splice_Rec_1962173,Human_Splice_Rec_1962179,Human_Splice_Rec_1962185,Human_Splice_Rec_1962189 111881 RMVar_ID_111881 Human_SNP_ID_833893120 m1A Human chr19 + 16190951 16190951 16190951 GCATTACGACATTCCCAAAGTCAGCTGGACGAAGTAGCCGCCTGCCCCCAGTATGGAGCAGCATC GCATTACGACATTCCCAAAGTCAGCTGGACGAGGTAGCCGCCTGCCCCCAGTATGGAGCAGCATC A G FAM32A Ensembl:ENSG00000105058 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr19:16190901..16191050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_6724831,Human_RBP_ID_9380752,Human_RBP_ID_18994534,Human_RBP_ID_26335946,Human_RBP_ID_27464668 Human_Splice_Rec_1973280,Human_Splice_Rec_1973286,Human_Splice_Rec_1973290,Human_Splice_Rec_1973298 111882 RMVar_ID_111882 Human_SNP_ID_833898162 m1A Human chr19 + 2216764 2216764 2216764 CCGGCAGGCCGGCTGCCAGTGAGCTGCATTCGAGGTGAGTGCCCTGGTGGGGCTGGGGGTCTGCA CCGGCAGGCCGGCTGCCAGTGAGCTGCATTCGTGGTGAGTGCCCTGGTGGGGCTGGGGGTCTGCA A T DOT1L Ensembl:ENSG00000104885 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:2216354..2220262 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_3954098,Human_RBP_ID_8839621,Human_RBP_ID_19088565,Human_RBP_ID_23257660 Human_Splice_Rec_1935153,Human_Splice_Rec_1935207 RMVar_hsa_circ_268586,RMVar_hsa_circ_119718,RMVar_hsa_circ_120678,RMVar_hsa_circ_102769,RMVar_hsa_circ_109532,RMVar_hsa_circ_101110,RMVar_hsa_circ_191188,RMVar_hsa_circ_191189,RMVar_hsa_circ_191186,RMVar_hsa_circ_191187,RMVar_hsa_circ_191185,RMVar_hsa_circ_123413,RMVar_hsa_circ_115808,RMVar_hsa_circ_191206,RMVar_hsa_circ_127010,RMVar_hsa_circ_107867,RMVar_hsa_circ_85658,RMVar_hsa_circ_77176,RMVar_hsa_circ_111617,RMVar_hsa_circ_191219,RMVar_hsa_circ_191220,RMVar_hsa_circ_191217,RMVar_hsa_circ_191218,RMVar_hsa_circ_191216,RMVar_hsa_circ_51545,RMVar_hsa_circ_191231,RMVar_hsa_circ_39463,RMVar_hsa_circ_7333,RMVar_hsa_circ_126584,RMVar_hsa_circ_191232,RMVar_hsa_circ_104042,RMVar_hsa_circ_78107,RMVar_hsa_circ_191234,RMVar_hsa_circ_191236 111883 RMVar_ID_111883 Human_SNP_ID_833899021 m1A Human chr19 - 54158330 54158330 54158330 CTGTTTCGGGAGCTGCTGGAGGAAGGGAAAGGAGTGATCAGAGGCAATAAAGAGTACAAGGAAGA CTGTTTCGGGAGCTGCTGGAGGAAGGGAAAGGTGTGATCAGAGGCAATAAAGAGTACAAGGAAGA T A LENG1 Ensembl:ENSG00000105617 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54158250..54158343 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_4546315 Human_Splice_Rec_2042395 111884 RMVar_ID_111884 Human_SNP_ID_833899822 m1A Human chr19 + 49157889 49157889 49157889 CCGCGGCAGCATGGTGGTGCCGGAGAAGGAGCAGGTGAGCGCCGGACCAGGGTCTGCGGGAGCGC CCGCGGCAGCATGGTGGTGCCGGAGAAGGAGCGGGTGAGCGCCGGACCAGGGTCTGCGGGAGCGC A G TRPM4 Ensembl:ENSG00000130529 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:49157839..49158390 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5145858,Human_RBP_ID_5320518,Human_RBP_ID_18420964,Human_RBP_ID_19093953 Human_Splice_Rec_2029053,Human_Splice_Rec_2029061,Human_Splice_Rec_2029099,Human_Splice_Rec_2029101,Human_Splice_Rec_2029149,Human_Splice_Rec_2029193,Human_Splice_Rec_2029239,Human_Splice_Rec_2029285 111885 RMVar_ID_111885 Human_SNP_ID_833902850 m1A Human chr19 - 10927821 10927821 10927821 AGGTGGCAGCTATGGAGCCGAGGATGAGGTGGAGGAGGAGAGTGACAAGGCCGCGGTGAGTCCCT AGGTGGCAGCTATGGAGCCGAGGATGAGGTGGTGGAGGAGAGTGACAAGGCCGCGGTGAGTCCCT T A YIPF2 Ensembl:ENSG00000130733 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:10927689..10927867 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus Human_RBP_ID_6718236,Human_RBP_ID_23781435,Human_RBP_ID_26337417 Human_Splice_Rec_1956737,Human_Splice_Rec_1956755,Human_Splice_Rec_1956791,Human_Splice_Rec_1956803,Human_Splice_Rec_1956829,Human_Splice_Rec_1956841,Human_Splice_Rec_1956851 RMVar_hsa_circ_84716,RMVar_hsa_circ_192472,RMVar_hsa_circ_192476,RMVar_hsa_circ_104361,RMVar_hsa_circ_122657,RMVar_hsa_circ_192477 111886 RMVar_ID_111886 Human_SNP_ID_833905399 m1A Human chr19 + 54191883 54191881 54191884 AGAAACTAGAACAGGCTTCAGGGGCCAGCTCAAGCCAGGAGGCCGGCTCGAGCCAGGCTGCCAAA AGAAACTAGAACAGGCTTCAGGGGCCAGCTC___CCAGGAGGCCGGCTCGAGCCAGGCTGCCAAA CAAG C TSEN34 Ensembl:ENSG00000170892 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:54191731..54191931 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 KIRC 1 - Human_RBP_ID_22449015 Human_Splice_Rec_2042625,Human_Splice_Rec_2042631,Human_Splice_Rec_2042637,Human_Splice_Rec_2042645,Human_Splice_Rec_2042655,Human_Splice_Rec_2042661,Human_Splice_Rec_2042669,Human_Splice_Rec_2042677,Human_Splice_Rec_2042681,Human_Splice_Rec_2042687 111887 RMVar_ID_111887 Human_SNP_ID_833908587 m1A Human chr19 + 47221527 47221527 47221527 GGTGGGCGGCAGAGGCGGGCGGCTCAGTCCCCACCCCCTCGGTCACCGCCACCTTCCGATGCTGA GGTGGGCGGCAGAGGCGGGCGGCTCAGTCCCCCCCCCCTCGGTCACCGCCACCTTCCGATGCTGA A C lnc-C5AR1-3 RNACentral:URS00008BE256 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:47221479..47221655 26863196 MeRIP-seq:(Medium) rs1038132968 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111888 RMVar_ID_111888 Human_SNP_ID_833911631 m1A Human chr19 + 46722063 46722063 46722063 TGACTGCGTCCAGGTGTGCAACCATGGAGTGCACCGGCTTACCTGAGGCGAGAAGGGCGGGTGGC TGACTGCGTCCAGGTGTGCAACCATGGAGTGCGCCGGCTTACCTGAGGCGAGAAGGGCGGGTGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:46721976..46722137 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 111889 RMVar_ID_111889 Human_SNP_ID_833919170 m1A Human chr19 - 35651294 35651294 35651294 CTAGTCTGGTTCTGGTTGGGGAAGCGGCTGTCAAAAGGGGCGGTCTTGTAGTTCTTGATTTTGGT CTAGTCTGGTTCTGGTTGGGGAAGCGGCTGTCGAAAGGGGCGGTCTTGTAGTTCTTGATTTTGGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr19:35651226..35651300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 6 kidney 111890 RMVar_ID_111890 Human_SNP_ID_833919282 m1A Human chr19 + 3585565 3585565 3585565 TGCAGGAAGCGGCGGATCCGGCGGCGGCGGCGAGGGCCCGGGTGGGTGGCCGAACTTCTCCCGCC TGCAGGAAGCGGCGGATCCGGCGGCGGCGGCGGGGGCCCGGGTGGGTGGCCGAACTTCTCCCGCC A G GIPC3 Ensembl:ENSG00000179855 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:3585533..3585763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 111891 RMVar_ID_111891 Human_SNP_ID_833919330 m1A Human chr19 + 8316599 8316599 8316599 GCGGCCATCGCGAGTGCAATAGTAATTGTTGGAGAGCTTGTGGCTAGGACCCACAGGGAGCTTGG GCGGCCATCGCGAGTGCAATAGTAATTGTTGGGGAGCTTGTGGCTAGGACCCACAGGGAGCTTGG A G lnc-RPS28-1,lnc-RPS28-1:2 RNACentral:URS00008C1243,RNACentral:URS00009BFB7E lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:8316548..8316687 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 111892 RMVar_ID_111892 Human_SNP_ID_833921665 m1A Human chr19 - 1236055 1236055 1236055 CCACCATGGCCACAGCCGCCACCACCACCACCACCACCACTGCCACAGTAGCCCTGACGACGTCG CCACCATGGCCACAGCCGCCACCACCACCACCTCCACCACTGCCACAGTAGCCCTGACGACGTCG T A CBARP Ensembl:ENSG00000099625 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:1236043..1237987 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_Splice_Rec_1931334,Human_Splice_Rec_1931335,Human_Splice_Rec_1931350,Human_Splice_Rec_1931351,Human_Splice_Rec_1931368,Human_Splice_Rec_1931369,Human_Splice_Rec_1931388,Human_Splice_Rec_1931389,Human_Splice_Rec_1931416,Human_Splice_Rec_1931417,Human_Splice_Rec_1931426,Human_Splice_Rec_1931427 RMVar_hsa_circ_53087 111893 RMVar_ID_111893 Human_SNP_ID_833926378 m1A Human chr19 + 45297727 45297727 45297727 CCCCCTGCCTCCCCCTCCAGTCACAGCCTGGCACCCCCATCAGGGGAGCGGAGCCGCCTGGCACG CCCCCTGCCTCCCCCTCCAGTCACAGCCTGGCGCCCCCATCAGGGGAGCGGAGCCGCCTGGCACG A G MARK4 Ensembl:ENSG00000007047 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:45297638..45297762 26863196 MeRIP-seq:(Medium) rs939611678 Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_21892762 Human_Splice_Rec_2018588,Human_Splice_Rec_2018620 RMVar_hsa_circ_93983,RMVar_hsa_circ_195297,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_121313,RMVar_hsa_circ_195318,RMVar_hsa_circ_42346 111894 RMVar_ID_111894 Human_SNP_ID_833933440 m1A Human chr19 - 18193334 18193334 18193334 TAGTGACGAGCAGCGCGCGGCCCTGGAATAGAAGCTGCCCCGCGGATAACAGGCGGCGTAGCCGG TAGTGACGAGCAGCGCGCGGCCCTGGAATAGACGCTGCCCCGCGGATAACAGGCGGCGTAGCCGG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr19:18193251..18193475 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 111895 RMVar_ID_111895 Human_SNP_ID_833933442 m1A Human chr19 - 46784584 46784584 46784584 ACAATGCTGCCCTCCCACTATGGTATCTAATAACCCTCTGTGTGTCTGTCTCTGCAGAAATATCT ACAATGCTGCCCTCCCACTATGGTATCTAATATCCCTCTGTGTGTCTGTCTCTGCAGAAATATCT T A SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:46784582..46784672 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_8490767,Human_RBP_ID_17928390,Human_RBP_ID_22665664,Human_RBP_ID_23802324 Human_Splice_Rec_2023067,Human_Splice_Rec_2023091,Human_Splice_Rec_2023105,Human_Splice_Rec_2023117,Human_Splice_Rec_2023127 RMVar_hsa_circ_106498,RMVar_hsa_circ_90411,RMVar_hsa_circ_195503,RMVar_hsa_circ_195502,RMVar_hsa_circ_80819,RMVar_hsa_circ_195515,RMVar_hsa_circ_99587,RMVar_hsa_circ_195522 111896 RMVar_ID_111896 Human_SNP_ID_833935724 m1A Human chr19 - 48497638 48497638 48497638 AAAGGCCGGATGGGTAGACAACACGAGGCCGCAGCCACCGCCGCCACCGCTGCCACCGCCACCGG AAAGGCCGGATGGGTAGACAACACGAGGCCGCCGCCACCGCCGCCACCGCTGCCACCGCCACCGG T G LMTK3 Ensembl:ENSG00000142235 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48497334..48497829 26863196 MeRIP-seq:(Medium) rs972769621 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5146024 RMVar_hsa_circ_103835,RMVar_hsa_circ_195696 111897 RMVar_ID_111897 Human_SNP_ID_833941020 m1A Human chr19 - 17324718 17324718 17324718 CTGGAAGCCCCCCGGCCCGAAGAGGAAGGCTCAGGTCACAAGCTTTAACTCGGGGGTGGGGACGC CTGGAAGCCCCCCGGCCCGAAGAGGAAGGCTCGGGTCACAAGCTTTAACTCGGGGGTGGGGACGC T C ANO8 Ensembl:ENSG00000074855 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:17323680..17324793 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 2 haematopoietic and lymphoid tissue Human_Splice_Rec_1976503,Human_Splice_Rec_1976535 RMVar_hsa_circ_102865,RMVar_hsa_circ_193306 111898 RMVar_ID_111898 Human_SNP_ID_833945463 m1A Human chr19 - 2419201 2419190 2419202 AGACTCCGTCAGAAAGAAAGAAACAGAGAGAAAGACAGAGAGAGAGAGAGAAGGAAAGGAAAGGA AGACTCCGTCAGAAAGAAAGAAACAGAGAGA____________GAGAGAGAAGGAAAGGAAAGGA CTCTCTCTGTCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:2419127..2419262 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..43 33 PAAD 1 - 111899 RMVar_ID_111899 Human_SNP_ID_833945634 m1A Human chr19 - 11384252 11384252 11384252 GACCCAGCTGTGGACTGTGCCGGGGGCGGGGGACGGAGGGGCAGGAGCCCTGGGCTCCCCGTGGC GACCCAGCTGTGGACTGTGCCGGGGGCGGGGGGCGGAGGGGCAGGAGCCCTGGGCTCCCCGTGGC T C EPOR Ensembl:ENSG00000187266 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:11384209..11384293 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4560095,Human_RBP_ID_21977709 111900 RMVar_ID_111900 Human_SNP_ID_833951404 m1A Human chr19 + 3207702 3207702 3207702 GAAGGCCAAGACACAGTGACACAGCCACCCCCACAGCCGGAGCCCCCGCCGCTCCACAGTCCCTG GAAGGCCAAGACACAGTGACACAGCCACCCCCGCAGCCGGAGCCCCCGCCGCTCCACAGTCCCTG A G NCLN Ensembl:ENSG00000125912 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:3207630..3207825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8255951,Human_RBP_ID_9380073 Human_Splice_Rec_1936938,Human_Splice_Rec_1936966,Human_Splice_Rec_1937002,Human_Splice_Rec_1937003,Human_Splice_Rec_1937020,Human_Splice_Rec_1937038,Human_Splice_Rec_1937040,Human_Splice_Rec_1937041 Human_miRNA_ID_2147304,Human_miRNA_ID_2988731,Human_miRNA_ID_3022430 RMVar_hsa_circ_23096,RMVar_hsa_circ_78683,RMVar_hsa_circ_78192,RMVar_hsa_circ_191326,RMVar_hsa_circ_191329 111901 RMVar_ID_111901 Human_SNP_ID_833954995 m1A Human chr19 + 17340378 17340378 17340378 GTTCTGATTAAGTCCTGCCCCCGGCCCTCCGGACATGTTTCTCATCCCTAAGCCCTCCGCCCAGC GTTCTGATTAAGTCCTGCCCCCGGCCCTCCGGGCATGTTTCTCATCCCTAAGCCCTCCGCCCAGC A G GTPBP3 Ensembl:ENSG00000130299 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:17340365..17340805;chr19:17340374..17340819 26863196 MeRIP-seq:(Medium) rs11666309 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1187732,Human_RBP_ID_13392209 RMVar_hsa_circ_106899,RMVar_hsa_circ_193311 111902 RMVar_ID_111902 Human_SNP_ID_833958233 m1A Human chr19 + 54145996 54145996 54145996 TCTTCAACCAGTCCAGCAGCACGCCCACCTCAACCACCTCCAGCTCTCCCATCCCGCCCAGCCCA TCTTCAACCAGTCCAGCAGCACGCCCACCTCACCCACCTCCAGCTCTCCCATCCCGCCCAGCCCA A C CNOT3 Ensembl:ENSG00000088038 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:54145890..54145996 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 4 head and neck Human_RBP_ID_9382870,Human_RBP_ID_22812074,Human_RBP_ID_26336757,Human_RBP_ID_26817965,Human_RBP_ID_27816694 Human_Splice_Rec_2042166,Human_Splice_Rec_2042167,Human_Splice_Rec_2042198,Human_Splice_Rec_2042199,Human_Splice_Rec_2042232,Human_Splice_Rec_2042233,Human_Splice_Rec_2042258,Human_Splice_Rec_2042259,Human_Splice_Rec_2042288,Human_Splice_Rec_2042289,Human_Splice_Rec_2042314,Human_Splice_Rec_2042315,Human_Splice_Rec_2042340,Human_Splice_Rec_2042341 111903 RMVar_ID_111903 Human_SNP_ID_833961741 m1A Human chr19 + 12952795 12952795 12952795 TGTGGAGGGGGAGGTGGGCGCCATAGGAGAGGAGGCCCCGCAGATGAACTACATCCAGGTGACGC TGTGGAGGGGGAGGTGGGCGCCATAGGAGAGGCGGCCCCGCAGATGAACTACATCCAGGTGACGC A C RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:12952744..12953023 26863196 MeRIP-seq:(Medium) rs1401343234 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_55567,Human_RBP_ID_513673,Human_RBP_ID_772891,Human_RBP_ID_1013189,Human_RBP_ID_5320188,Human_RBP_ID_5585375,Human_RBP_ID_22977670,Human_RBP_ID_23114764,Human_RBP_ID_23130714,Human_RBP_ID_23783111 Human_Splice_Rec_1964435,Human_Splice_Rec_1964451,Human_Splice_Rec_1964467,Human_Splice_Rec_1964493,Human_Splice_Rec_1964523,Human_Splice_Rec_1964543,Human_Splice_Rec_1964549,Human_Splice_Rec_1964551 Human_miRNA_ID_1091017 RMVar_hsa_circ_41260 111904 RMVar_ID_111904 Human_SNP_ID_833963622 m1A Human chr19 - 7519547 7519547 7519547 GGGTGTCGCTGTTAGGATCGAGAATCAGGGGTACGGGGCCAATCACATCTGGATCGAGGTCGAAA GGGTGTCGCTGTTAGGATCGAGAATCAGGGGTGCGGGGCCAATCACATCTGGATCGAGGTCGAAA T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:7519426..7519622 26863410 MeRIP-seq:(Medium) rs1214676315 Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 111905 RMVar_ID_111905 Human_SNP_ID_833966937 m1A Human chr19 - 40613927 40613927 40613927 GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCACTCGTCAACGTCTGCGGGACAGGGCGTCCGAA GATGCCGCTCTGGCAAAGGTCCTCCTCGCTGCGCTCGTCAACGTCTGCGGGACAGGGCGTCCGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr19:40613377..40613955 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 111906 RMVar_ID_111906 Human_SNP_ID_833968023 m1A Human chr19 + 6415100 6415100 6415100 CTAAGGCAGGATGGACGGTGGCCGGGGGTTGGAAGGAGAAAGGAGGAGGAGGAGGGTGGCAATTC CTAAGGCAGGATGGACGGTGGCCGGGGGTTGGGAGGAGAAAGGAGGAGGAGGAGGGTGGCAATTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:6415051..6415100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 111907 RMVar_ID_111907 Human_SNP_ID_833980282 m1A Human chr19 - 49615879 49615879 49615879 TCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCAGGAGTCTGCTCTGGGGGCTTCTCAGATGTCGT TCGGGGGCAGGGGGCTCAGGCATGGCCGTCTCGGGAGTCTGCTCTGGGGGCTTCTCAGATGTCGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:49615749..49616095 26863196 MeRIP-seq:(Medium) rs778558246 Functional Loss SNV ICGC 33..33 33 STAD 1 - 111908 RMVar_ID_111908 Human_SNP_ID_833980823 m1A Human chr19 + 12940403 12940403 12940403 GATAAAGGATCCTGATGCTTCAAAACCGGAAGACTGGGATGAGCGGGCCAAGATCGATGATCCCA GATAAAGGATCCTGATGCTTCAAAACCGGAAGTCTGGGATGAGCGGGCCAAGATCGATGATCCCA A T CALR Ensembl:ENSG00000179218 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_772182,Human_RBP_ID_914234,Human_RBP_ID_1554869,Human_RBP_ID_1880261,Human_RBP_ID_4562177,Human_RBP_ID_5194164,Human_RBP_ID_5585363,Human_RBP_ID_6721312,Human_RBP_ID_8477492,Human_RBP_ID_9380595,Human_RBP_ID_13372368,Human_RBP_ID_17694627,Human_RBP_ID_18440574,Human_RBP_ID_18532272,Human_RBP_ID_18722832,Human_RBP_ID_22447472,Human_RBP_ID_22762818,Human_RBP_ID_22809293,Human_RBP_ID_22978416,Human_RBP_ID_23783067,Human_RBP_ID_26334871,Human_RBP_ID_27463669 Human_Splice_Rec_1964385,Human_Splice_Rec_1964405,Human_Splice_Rec_1964409 RMVar_hsa_circ_75759,RMVar_hsa_circ_192837,RMVar_hsa_circ_127216,RMVar_hsa_circ_77416,RMVar_hsa_circ_192836,RMVar_hsa_circ_369902,RMVar_hsa_circ_106916,RMVar_hsa_circ_192839,RMVar_hsa_circ_192840,RMVar_hsa_circ_108819,RMVar_hsa_circ_83331,RMVar_hsa_circ_88629,RMVar_hsa_circ_110485,RMVar_hsa_circ_192842,RMVar_hsa_circ_192843,RMVar_hsa_circ_192841,RMVar_hsa_circ_105835,RMVar_hsa_circ_331796,RMVar_hsa_circ_192844,RMVar_hsa_circ_192845,RMVar_hsa_circ_192846,RMVar_hsa_circ_361141,RMVar_hsa_circ_364158,RMVar_hsa_circ_64986,RMVar_hsa_circ_107375,RMVar_hsa_circ_192847 111909 RMVar_ID_111909 Human_SNP_ID_833981032 m1A Human chr19 + 19516293 19516293 19516293 AGGACATGCCTCCGCCGGGGGGCTATGGGCCCATCGACTACAAACGGAACTTGCCGCGTCGAGGA AGGACATGCCTCCGCCGGGGGGCTATGGGCCCGTCGACTACAAACGGAACTTGCCGCGTCGAGGA A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:19516226..19526275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung Human_RBP_ID_138703,Human_RBP_ID_240752,Human_RBP_ID_1556827,Human_RBP_ID_4512358,Human_RBP_ID_5116830,Human_RBP_ID_9085183,Human_RBP_ID_9328860,Human_RBP_ID_17656050,Human_RBP_ID_17917580,Human_RBP_ID_22446620,Human_RBP_ID_26336088,Human_RBP_ID_27815333 Human_Splice_Rec_1983479,Human_Splice_Rec_1983487,Human_Splice_Rec_1983495,Human_Splice_Rec_1983503,Human_Splice_Rec_1983505,Human_Splice_Rec_1983511,Human_Splice_Rec_1983515,Human_Splice_Rec_1983523,Human_Splice_Rec_1983535 RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 111910 RMVar_ID_111910 Human_SNP_ID_833987079 m1A Human chr19 - 48391500 48391500 48391500 CCGCCAGCTCCAGCCTTTGCTCCCCCTCCCAAAGTCCCCTCCCCGGAGCGGAGCGCACCTAGGGT CCGCCAGCTCCAGCCTTTGCTCCCCCTCCCAACGTCCCCTCCCCGGAGCGGAGCGCACCTAGGGT T G KDELR1 Ensembl:ENSG00000105438 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr19:48391245..48391557;chr19:48391301..48391550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_55142,Human_RBP_ID_241380,Human_RBP_ID_524865,Human_RBP_ID_773685,Human_RBP_ID_4540636,Human_RBP_ID_5421726,Human_RBP_ID_5443320,Human_RBP_ID_5469015,Human_RBP_ID_5499909,Human_RBP_ID_17386956,Human_RBP_ID_18947179,Human_RBP_ID_22237284,Human_RBP_ID_22533187,Human_RBP_ID_23803732,Human_RBP_ID_26993028,Human_RBP_ID_27276671 111911 RMVar_ID_111911 Human_SNP_ID_833987650 m1A Human chr19 + 39433568 39433568 39433568 GCCACCAGGGCTTTGGAGATGGACTGACGGATAGCTGTGAGAAAGACACACAATTAAAGGGTACA GCCACCAGGGCTTTGGAGATGGACTGACGGATGGCTGTGAGAAAGACACACAATTAAAGGGTACA A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr19:39433501..39433575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111912 RMVar_ID_111912 Human_SNP_ID_833988131 m1A Human chr19 - 12721435 12721435 12721435 GCAGAGTGTCGGGGGAAGGGGACTCTTCAGGGACTGTGCCTGCATAGAAGAGACCACGGGGGCCG GCAGAGTGTCGGGGGAAGGGGACTCTTCAGGGTCTGTGCCTGCATAGAAGAGACCACGGGGGCCG T A TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:12721432..12722035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 5 biliary tract,gallbladder Human_RBP_ID_825385,Human_RBP_ID_3580876,Human_RBP_ID_6720934,Human_RBP_ID_17190812,Human_RBP_ID_23782766 RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192741,RMVar_hsa_circ_192763,RMVar_hsa_circ_102292,RMVar_hsa_circ_101720,RMVar_hsa_circ_192764,RMVar_hsa_circ_192765,RMVar_hsa_circ_192772,RMVar_hsa_circ_116785,RMVar_hsa_circ_192774,RMVar_hsa_circ_372945 111913 RMVar_ID_111913 Human_SNP_ID_833989919 m1A Human chr19 - 55262651 55262651 55262651 GGAGGAGCTGGAGTTCTGTGAAAAGCTGCTACAGACCTGTTTCTCCAGCCCAGCGGACGACAGCA GGAGGAGCTGGAGTTCTGTGAAAAGCTGCTACGGACCTGTTTCTCCAGCCCAGCGGACGACAGCA T C HSPBP1 Ensembl:ENSG00000133265 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:55262600..55262725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_1891747,Human_RBP_ID_17657351 Human_Splice_Rec_2047046,Human_Splice_Rec_2047062,Human_Splice_Rec_2047074,Human_Splice_Rec_2047080 RMVar_hsa_circ_112241,RMVar_hsa_circ_196311,RMVar_hsa_circ_110233,RMVar_hsa_circ_196310 111914 RMVar_ID_111914 Human_SNP_ID_833990008 m1A Human chr19 - 1592715 1592710 1592716 CAGCCGCGGCAAGTGGCGGCGGCGGCAGCGGCAGCGGAGGCAGCTGAGGCGGCGGCGGCGAGTGG CAGCCGCGGCAAGTGGCGGCGGCGGCAGCGG______AGGCAGCTGAGGCGGCGGCGGCGAGTGG TCCGCTG T MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr19:1592601..1592800 26863410 MeRIP-seq:(Medium) rs1012473361 Functional Loss DEL ICGC 32..37 33 STAD 1 - Human_RBP_ID_4557010,Human_RBP_ID_5320900,Human_RBP_ID_8942116,Human_RBP_ID_9328113,Human_RBP_ID_9425653,Human_RBP_ID_13383927,Human_RBP_ID_26471600 Human_Splice_Rec_1933381 111915 RMVar_ID_111915 Human_SNP_ID_833991218 m1A Human chr19 - 48171933 48171933 48171933 GCGCCAGGTGCATGGAGCTCTTGACGAAGAAGAGCGCCAGCCGCTGCTGGCACCACGCGTCGAAG GCGCCAGGTGCATGGAGCTCTTGACGAAGAAGGGCGCCAGCCGCTGCTGGCACCACGCGTCGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:48171744..48171964 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111916 RMVar_ID_111916 Human_SNP_ID_833994242 m1A Human chr19 - 7620656 7620656 7620656 CCCCAACCCCGGTGTCCAGGTGCTGTCGGACGAGCACGCGCGTGAGATGTGCCTGCGGTTTGCAG CCCCAACCCCGGTGTCCAGGTGCTGTCGGACGTGCACGCGCGTGAGATGTGCCTGCGGTTTGCAG T A XAB2 Ensembl:ENSG00000076924 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:7620607..7621033 32194978 MeRIP-seq:(Medium) rs1168841877 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_770086,Human_RBP_ID_8839684,Human_RBP_ID_9293286 Human_Splice_Rec_1947754,Human_Splice_Rec_1947778,Human_Splice_Rec_1947786 RMVar_hsa_circ_91906,RMVar_hsa_circ_113541,RMVar_hsa_circ_192004,RMVar_hsa_circ_97638,RMVar_hsa_circ_192005,RMVar_hsa_circ_112031,RMVar_hsa_circ_82042,RMVar_hsa_circ_192006,RMVar_hsa_circ_95608,RMVar_hsa_circ_192007,RMVar_hsa_circ_192008,RMVar_hsa_circ_192009 111917 RMVar_ID_111917 Human_SNP_ID_834000365 m1A Human chr19 - 18532717 18532717 18532717 AGCGGAGCACGGAGACCGCCTTGTACCGGAAAATGCTGGGCAACCCCAGCCGGCTGCCTGCTAAG AGCGGAGCACGGAGACCGCCTTGTACCGGAAAGTGCTGGGCAACCCCAGCCGGCTGCCTGCTAAG T C FKBP8 Ensembl:ENSG00000105701 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:18532637..18532736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_516278,Human_RBP_ID_17267159 Human_Splice_Rec_1980470,Human_Splice_Rec_1980471,Human_Splice_Rec_1980478,Human_Splice_Rec_1980479,Human_Splice_Rec_1980494,Human_Splice_Rec_1980495,Human_Splice_Rec_1980508,Human_Splice_Rec_1980509,Human_Splice_Rec_1980522,Human_Splice_Rec_1980523,Human_Splice_Rec_1980536,Human_Splice_Rec_1980537,Human_Splice_Rec_1980542,Human_Splice_Rec_1980543,Human_Splice_Rec_1980548,Human_Splice_Rec_1980549 RMVar_hsa_circ_45679,RMVar_hsa_circ_45041 111918 RMVar_ID_111918 Human_SNP_ID_834000780 m1A Human chr19 - 55685502 55685502 55685502 CGTTCACGCCCTGGTCCTTGCCGTCGCGGTCCACGTACTGGAAGTCCTTCAGCGTCTGCACGGCG CGTTCACGCCCTGGTCCTTGCCGTCGCGGTCCGCGTACTGGAAGTCCTTCAGCGTCTGCACGGCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55685451..55685682 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 111919 RMVar_ID_111919 Human_SNP_ID_834011666 m1A Human chr19 + 35575732 35575732 35575732 TGCCGAATCAACTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCC TGCCGAATCAACTAGCCCTGAAAATGGATGGCGCTGGAGCATCAGGCCCATACCCGGCCATCGCC A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62109965 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_1064019,Human_RBP_ID_5190631,Human_RBP_ID_5293555,Human_RBP_ID_5421445,Human_RBP_ID_5443003,Human_RBP_ID_5499418,Human_RBP_ID_8096729,Human_RBP_ID_17063375,Human_RBP_ID_17921490,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26467462,Human_RBP_ID_26749474,Human_RBP_ID_27157562 111920 RMVar_ID_111920 Human_SNP_ID_834012342 m1A Human chr19 - 45770199 45770199 45770199 CTGCTGCTGCTGCTGCTGCTGCTGCTGGGGGGATCACAGACCATTTCTTTCTTTCGGCCAGGCTG CTGCTGCTGCTGCTGCTGCTGCTGCTGGGGGGCTCACAGACCATTTCTTTCTTTCGGCCAGGCTG T G DMPK Ensembl:ENSG00000104936 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:45770163..45770660 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5321745,Human_RBP_ID_22666753,Human_RBP_ID_26472655 111921 RMVar_ID_111921 Human_SNP_ID_834013346 m1A Human chr19 + 5679728 5679728 5679728 GCCCCAGCAGCTCCTGGTCGTACACCAGGTAGACGGCGCCCCCAGCCACACTTCCCTTGATGAGG GCCCCAGCAGCTCCTGGTCGTACACCAGGTAGGCGGCGCCCCCAGCCACACTTCCCTTGATGAGG A G RPL36 Ensembl:ENSG00000130255 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:5679570..5680057 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111922 RMVar_ID_111922 Human_SNP_ID_834016857 m1A Human chr19 - 17226948 17226948 17226948 CGTGGTCTGGAGTTAAATCGGGGTGTCGGGAAACCGGAGTCCCTCAAACTGGAGGGGCTAAATCT CGTGGTCTGGAGTTAAATCGGGGTGTCGGGAATCCGGAGTCCCTCAAACTGGAGGGGCTAAATCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr19:17226943..17227075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 111923 RMVar_ID_111923 Human_SNP_ID_834018037 m1A Human chr19 - 55112752 55112752 55112752 TGAGAACCTGGAGGTGGTGCGCTTCTTGGTGGAGCAGGGCGCCACTGTGAACCAGGCAGACAACG TGAGAACCTGGAGGTGGTGCGCTTCTTGGTGGTGCAGGGCGCCACTGTGAACCAGGCAGACAACG T A PPP1R12C Ensembl:ENSG00000125503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr19:55112701..55112832 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_8560,Human_RBP_ID_3955587,Human_RBP_ID_9382903,Human_RBP_ID_17930882,Human_RBP_ID_18739165,Human_RBP_ID_18995452 Human_Splice_Rec_2045954,Human_Splice_Rec_2045955,Human_Splice_Rec_2046002,Human_Splice_Rec_2046003,Human_Splice_Rec_2046044,Human_Splice_Rec_2046045 Human_miRNA_ID_2381580,Human_miRNA_ID_3024590 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_330329,RMVar_hsa_circ_121044,RMVar_hsa_circ_52214,RMVar_hsa_circ_196271 111924 RMVar_ID_111924 Human_SNP_ID_834018877 m1A Human chr19 - 40765199 40765199 40765199 TGAGCCAAGGGGGAAAGGGGTGGCCCCAGAACAGGGGAAGGGGCAGGCATGGGGGGAAAAGGTGC TGAGCCAAGGGGGAAAGGGGTGGCCCCAGAACGGGGGAAGGGGCAGGCATGGGGGGAAAAGGTGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr19:40765176..40765200 26863196 MeRIP-seq:(Medium) rs13108 Functional Loss SNV ICGC 33..33 33 COCA 5 - 111925 RMVar_ID_111925 Human_SNP_ID_834021401 m1A Human chr19 - 46727478 46727478 46727478 TGAGCCTGGGGGACTTGGCAGATCTCACCGTCACCAACGACAACGACCTCAGCTGCGATGTAAGT TGAGCCTGGGGGACTTGGCAGATCTCACCGTCTCCAACGACAACGACCTCAGCTGCGATGTAAGT T A STRN4 Ensembl:ENSG00000090372 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr19:46727451..46727550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_52837,Human_RBP_ID_907922,Human_RBP_ID_8490673,Human_RBP_ID_8835650,Human_RBP_ID_13480134 Human_Splice_Rec_2022628,Human_Splice_Rec_2022629,Human_Splice_Rec_2022662,Human_Splice_Rec_2022663,Human_Splice_Rec_2022712,Human_Splice_Rec_2022713,Human_Splice_Rec_2022744,Human_Splice_Rec_2022745,Human_Splice_Rec_2022761,Human_Splice_Rec_2022774,Human_Splice_Rec_2022775,Human_Splice_Rec_2022790,Human_Splice_Rec_2022791,Human_Splice_Rec_2022813,Human_Splice_Rec_2022836,Human_Splice_Rec_2022837,Human_Splice_Rec_2022845,Human_Splice_Rec_2022852 RMVar_hsa_circ_82942,RMVar_hsa_circ_93181,RMVar_hsa_circ_125207,RMVar_hsa_circ_195495,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195497,RMVar_hsa_circ_195499 111926 RMVar_ID_111926 Human_SNP_ID_834030948 m1A Human chr19 - 9838591 9838590 9838591 CTTGGTCCGGGTGATCTTCTCCTGCCGCCAGGACGAGGGCCGCCGTGACTGGCTGTGCTTCACCA CTTGGTCCGGGTGATCTTCTCCTGCCGCCAGG_CGAGGGCCGCCGTGACTGGCTGTGCTTCACCA GT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr19:9838426..9848164 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 SARC 1 - 111927 RMVar_ID_111927 Human_SNP_ID_834032883 m1A Human chr19 + 13772567 13772567 13772567 ATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ATGTGGATAACAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1376233591 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_miRNA_ID_1358389,Human_miRNA_ID_1694158,Human_miRNA_ID_2320072,Human_miRNA_ID_2326405,Human_miRNA_ID_2520781,Human_miRNA_ID_2523948,Human_miRNA_ID_2775777,Human_miRNA_ID_2836545,Human_miRNA_ID_2891200 RMVar_hsa_circ_192922,RMVar_hsa_circ_192921,RMVar_hsa_circ_88611,RMVar_hsa_circ_110431,RMVar_hsa_circ_89922,RMVar_hsa_circ_114914,RMVar_hsa_circ_192925,RMVar_hsa_circ_192927 111928 RMVar_ID_111928 Human_SNP_ID_823434691 m1A Human chr15 - 70832777 70832777 70832777 CCCCTGACATCCGGAGGATCAGCAGCCGCTACAGCCAAGTGGGGACCCAGGAGTGCGCCATCGTG CCCCTGACATCCGGAGGATCAGCAGCCGCTACTGCCAAGTGGGGACCCAGGAGTGCGCCATCGTG T A LARP6 Ensembl:ENSG00000166173 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70832726..70832875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver RMVar_hsa_circ_118230,RMVar_hsa_circ_173516 111929 RMVar_ID_111929 Human_SNP_ID_823466202 m1A Human chr15 - 51966082 51966082 51966082 AAAGTGACCAGTCAGATGATGAAAAGATACAAAATTCTGATGATGAGGAGAGGGCACAAGGATCT AAAGTGACCAGTCAGATGATGAAAAGATACAACATTCTGATGATGAGGAGAGGGCACAAGGATCT T G LEO1 Ensembl:ENSG00000166477 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:51965926..51966226 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_43318,Human_RBP_ID_2444160,Human_RBP_ID_8080275,Human_RBP_ID_9283058,Human_RBP_ID_17861968 Human_miRNA_ID_584012 RMVar_hsa_circ_71926,RMVar_hsa_circ_30577,RMVar_hsa_circ_74964,RMVar_hsa_circ_367935 111930 RMVar_ID_111930 Human_SNP_ID_823481228 m1A Human chr15 + 31327715 31327715 31327715 CGCCGACCTCGAGTCCCCGCAGAGGAAGCACAAGTGCCACTACGCGGGCTGCGAGAAAGTTTACG CGCCGACCTCGAGTCCCCGCAGAGGAAGCACACGTGCCACTACGCGGGCTGCGAGAAAGTTTACG A C KLF13 Ensembl:ENSG00000169926 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:31327598..31327717 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_Splice_Rec_1577129,Human_Splice_Rec_1577131 Human_miRNA_ID_2237356 RMVar_hsa_circ_127198,RMVar_hsa_circ_170460 111931 RMVar_ID_111931 Human_SNP_ID_823486779 m1A Human chr15 + 44711582 44711567 44711583 TCTCGCTCCGTGGCCTTAGCTGTGCTCGCGCTACTCTCTCTTTCTGGCCTGGAGGCTATCCAGCG TCTCGCTCCGTGGCCTTA________________TCTCTCTTTCTGGCCTGGAGGCTATCCAGCG AGCTGTGCTCGCGCTAC A B2M Ensembl:ENSG00000166710 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:44711501..44711679;chr15:44711501..44711664 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 19..34 33 DLBC 2 - Human_RBP_ID_42487,Human_RBP_ID_232273,Human_RBP_ID_298354,Human_RBP_ID_458100,Human_RBP_ID_759128,Human_RBP_ID_815149,Human_RBP_ID_887565,Human_RBP_ID_1000773,Human_RBP_ID_1504960,Human_RBP_ID_3475157,Human_RBP_ID_4323350,Human_RBP_ID_5316071,Human_RBP_ID_5494390,Human_RBP_ID_6429621,Human_RBP_ID_8417302,Human_RBP_ID_9324257,Human_RBP_ID_17187745,Human_RBP_ID_17482241,Human_RBP_ID_18663312,Human_RBP_ID_20003791,Human_RBP_ID_22439776,Human_RBP_ID_22759583,Human_RBP_ID_23653066,Human_RBP_ID_24473603,Human_RBP_ID_25142108,Human_RBP_ID_26931775,Human_RBP_ID_27435378,Human_RBP_ID_27559415 Human_Splice_Rec_1596093,Human_Splice_Rec_1596097,Human_Splice_Rec_1596103,Human_Splice_Rec_1596111,Human_Splice_Rec_1596119,Human_Splice_Rec_1596125 RMVar_hsa_circ_171696,RMVar_hsa_circ_121594 111932 RMVar_ID_111932 Human_SNP_ID_823494528 m1A Human chr15 - 60382401 60382401 60382401 ACCCCCAAGTGCATATGGGTCTGTCAAAGCCTATACTAACTTTGATGCTGAGCGGGATGCTTTGA ACCCCCAAGTGCATATGGGTCTGTCAAAGCCTGTACTAACTTTGATGCTGAGCGGGATGCTTTGA T C ANXA2 Ensembl:ENSG00000182718 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:60382360..60382431 26863196 MeRIP-seq:(Medium) rs747064927 Functional Loss SNV ICGC,COSMIC 33..33 33 OV,lung adenocarcinoma,ovary serous_carcinoma 9 lung,ovary Human_RBP_ID_4326687,Human_RBP_ID_18189562,Human_RBP_ID_22440634,Human_RBP_ID_27435841 Human_Splice_Rec_1608742,Human_Splice_Rec_1608743,Human_Splice_Rec_1608766,Human_Splice_Rec_1608767,Human_Splice_Rec_1608790,Human_Splice_Rec_1608791,Human_Splice_Rec_1608811,Human_Splice_Rec_1608830,Human_Splice_Rec_1608831,Human_Splice_Rec_1608854,Human_Splice_Rec_1608855,Human_Splice_Rec_1608926,Human_Splice_Rec_1608927,Human_Splice_Rec_1608958,Human_Splice_Rec_1608959,Human_Splice_Rec_1608978,Human_Splice_Rec_1608979,Human_Splice_Rec_1608998,Human_Splice_Rec_1608999,Human_Splice_Rec_1609024,Human_Splice_Rec_1609025,Human_Splice_Rec_1609036,Human_Splice_Rec_1609037,Human_Splice_Rec_1609050,Human_Splice_Rec_1609051,Human_Splice_Rec_1609078,Human_Splice_Rec_1609079,Human_Splice_Rec_1609104,Human_Splice_Rec_1609105,Human_Splice_Rec_1609116,Human_Splice_Rec_1609117,Human_Splice_Rec_1609128,Human_Splice_Rec_1609129,Human_Splice_Rec_1609144,Human_Splice_Rec_1609145,Human_Splice_Rec_1609154,Human_Splice_Rec_1609155,Human_Splice_Rec_1609164,Human_Splice_Rec_1609165,Human_Splice_Rec_1609174,Human_Splice_Rec_1609175,Human_Splice_Rec_1609190,Human_Splice_Rec_1609191,Human_Splice_Rec_1609198,Human_Splice_Rec_1609199,Human_Splice_Rec_1609208,Human_Splice_Rec_1609209,Human_Splice_Rec_1609218 RMVar_hsa_circ_93056,RMVar_hsa_circ_51075,RMVar_hsa_circ_111674,RMVar_hsa_circ_124678,RMVar_hsa_circ_374625,RMVar_hsa_circ_172543,RMVar_hsa_circ_96765,RMVar_hsa_circ_172549,RMVar_hsa_circ_6297,RMVar_hsa_circ_172550,RMVar_hsa_circ_172551,RMVar_hsa_circ_2198,RMVar_hsa_circ_105218,RMVar_hsa_circ_52898,RMVar_hsa_circ_172552,RMVar_hsa_circ_322584,RMVar_hsa_circ_282085,RMVar_hsa_circ_325479,RMVar_hsa_circ_172559,RMVar_hsa_circ_172560,RMVar_hsa_circ_326773,RMVar_hsa_circ_367664,RMVar_hsa_circ_172561,RMVar_hsa_circ_172563,RMVar_hsa_circ_47446,RMVar_hsa_circ_273183,RMVar_hsa_circ_172562,RMVar_hsa_circ_292240,RMVar_hsa_circ_172564,RMVar_hsa_circ_114795,RMVar_hsa_circ_172567,RMVar_hsa_circ_307579,RMVar_hsa_circ_346419,RMVar_hsa_circ_172568,RMVar_hsa_circ_292600,RMVar_hsa_circ_277326,RMVar_hsa_circ_117179,RMVar_hsa_circ_91465,RMVar_hsa_circ_172570,RMVar_hsa_circ_172571,RMVar_hsa_circ_172572,RMVar_hsa_circ_172569 111933 RMVar_ID_111933 Human_SNP_ID_823512381 m1A Human chr15 + 90530021 90530021 90530021 GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTACAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC GGCGGCCTGTGGACGGACGGGTGGGCCGAGGTGCAGGCCCCACGGCCGCCGTCTCCCGCTTCTGC A G CRTC3 Ensembl:ENSG00000140577 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:90529901..90530175 26863196 MeRIP-seq:(Medium) rs910957497 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4340052,Human_RBP_ID_17367011 111934 RMVar_ID_111934 Human_SNP_ID_823520616 m1A Human chr15 + 63121884 63121884 63121884 GCCGGCTGTGCAGAGACGCCATGTACCGGCTCATGTCAGCAGTGACTGCCCGGGCTGCCGCCCCC GCCGGCTGTGCAGAGACGCCATGTACCGGCTCCTGTCAGCAGTGACTGCCCGGGCTGCCGCCCCC A C LACTB Ensembl:ENSG00000103642 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:63121850..63122123 26863196 MeRIP-seq:(Medium) rs34317102 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_4342721,Human_RBP_ID_8804078,Human_RBP_ID_9283659 GWAS_ID_12660,GWAS_ID_12661,GWAS_ID_12662,GWAS_ID_12663,GWAS_ID_12664,GWAS_ID_12665,GWAS_ID_12666,GWAS_ID_12667,GWAS_ID_12668,GWAS_ID_12669,GWAS_ID_12670,GWAS_ID_12671,GWAS_ID_12672,GWAS_ID_12673,GWAS_ID_12674,GWAS_ID_12675,GWAS_ID_12676,GWAS_ID_12677,GWAS_ID_12678,GWAS_ID_12679,GWAS_ID_12680,GWAS_ID_12681,GWAS_ID_12682,GWAS_ID_12683,GWAS_ID_12684,GWAS_ID_12685,GWAS_ID_12686,GWAS_ID_12687,GWAS_ID_12688,GWAS_ID_12689,GWAS_ID_12690,GWAS_ID_12691,GWAS_ID_12692,GWAS_ID_12693,GWAS_ID_12694,GWAS_ID_12695,GWAS_ID_12696,GWAS_ID_12697,GWAS_ID_12698,GWAS_ID_12699,GWAS_ID_12700,GWAS_ID_12701,GWAS_ID_12702,GWAS_ID_12703,GWAS_ID_12704,GWAS_ID_12705,GWAS_ID_12706,GWAS_ID_12707,GWAS_ID_12708,GWAS_ID_12709,GWAS_ID_12710,GWAS_ID_12711,GWAS_ID_12712,GWAS_ID_12713,GWAS_ID_12714,GWAS_ID_12715,GWAS_ID_12716,GWAS_ID_12717,GWAS_ID_12718,GWAS_ID_12719 111935 RMVar_ID_111935 Human_SNP_ID_823522013 m1A Human chr15 + 41847419 41847419 41847419 ACCCATCTCGCCCAGCCCCGAAGAGCAGCTCCAGCCTCGGGAGTGCCACACCTTCTCCGACCCCA ACCCATCTCGCCCAGCCCCGAAGAGCAGCTCCGGCCTCGGGAGTGCCACACCTTCTCCGACCCCA A G JMJD7-PLA2G4B,PLA2G4B Ensembl:ENSG00000168970,Ensembl:ENSG00000243708 Protein coding,Protein coding exon,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:41847394..41847533 26863196 MeRIP-seq:(Medium) rs776135432 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver Human_Splice_Rec_1588102,Human_Splice_Rec_1588148,Human_Splice_Rec_1588192,Human_Splice_Rec_1588280,Human_Splice_Rec_1588318,Human_Splice_Rec_1588370,Human_Splice_Rec_1588392 RMVar_hsa_circ_113092,RMVar_hsa_circ_116729,RMVar_hsa_circ_171155,RMVar_hsa_circ_171156 111936 RMVar_ID_111936 Human_SNP_ID_823527477 m1A Human chr15 + 64848504 64848504 64848504 CACATATTATGATGTCATTAGGTACTTAGCCTAGGGACACATCCCTTGTGTGACCTATGAACCTG CACATATTATGATGTCATTAGGTACTTAGCCTGGGGACACATCCCTTGTGTGACCTATGAACCTG A G AC069368.1,PLEKHO2 Ensembl:ENSG00000249240,Ensembl:ENSG00000241839 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:64848486..64848650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 2 - 111937 RMVar_ID_111937 Human_SNP_ID_823550665 m1A Human chr15 + 69455250 69455250 69455250 GGTGGACCTGCTCCAGCAGCTGGTGCTGCACCAGCAGGAGGTCCTGCCCCCTCCACTGCTGCTGC GGTGGACCTGCTCCAGCAGCTGGTGCTGCACCGGCAGGAGGTCCTGCCCCCTCCACTGCTGCTGC A G RPLP1 Ensembl:ENSG00000137818 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:69455199..69455408 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_232117,Human_RBP_ID_462541,Human_RBP_ID_814831,Human_RBP_ID_886604,Human_RBP_ID_1507541,Human_RBP_ID_4343238,Human_RBP_ID_8421561,Human_RBP_ID_9055739,Human_RBP_ID_9324559,Human_RBP_ID_17652167,Human_RBP_ID_18666979,Human_RBP_ID_22440364,Human_RBP_ID_23162220,Human_RBP_ID_26933733 Human_Splice_Rec_1618846,Human_Splice_Rec_1618847,Human_Splice_Rec_1618852,Human_Splice_Rec_1618853,Human_Splice_Rec_1618857,Human_Splice_Rec_1618862,Human_Splice_Rec_1618863 Human_miRNA_ID_1998567,Human_miRNA_ID_2052145,Human_miRNA_ID_2512578,Human_miRNA_ID_3055401 RMVar_hsa_circ_92534,RMVar_hsa_circ_109341,RMVar_hsa_circ_114312,RMVar_hsa_circ_173479,RMVar_hsa_circ_173480,RMVar_hsa_circ_93094,RMVar_hsa_circ_173481,RMVar_hsa_circ_173482 111938 RMVar_ID_111938 Human_SNP_ID_823552734 m1A Human chr15 - 90629415 90629415 90629415 GTGAGAGGGCTGACGGGAGGCTGCCGACGCCGAGACGGGCCGCTCAGGTTTGTGGTGGAAAGAGA GTGAGAGGGCTGACGGGAGGCTGCCGACGCCGGGACGGGCCGCTCAGGTTTGTGGTGGAAAGAGA T C CRTC3-AS1 Ensembl:ENSG00000259736 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr15:90629294..90637901;chr15:90629276..90629550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 111939 RMVar_ID_111939 Human_SNP_ID_823560405 m1A Human chr15 + 75658320 75658320 75658320 TCTTCCCAAGATCCTTCCTGTTGCACAATGGGAAACCTAAGAGGAAAAAGACAGGGGCCTGCTTG TCTTCCCAAGATCCTTCCTGTTGCACAATGGGGAACCTAAGAGGAAAAAGACAGGGGCCTGCTTG A G SNX33 Ensembl:ENSG00000173548 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75658272..75658571 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_26437783 RMVar_hsa_circ_94621,RMVar_hsa_circ_90405,RMVar_hsa_circ_173992,RMVar_hsa_circ_110616,RMVar_hsa_circ_173993,RMVar_hsa_circ_173994 111940 RMVar_ID_111940 Human_SNP_ID_823584253 m1A Human chr15 + 40386324 40386324 40386324 TCTGTTTGTTACAGGGTTGCAACTGTCGGGTCATGATGCCAGAAGCTTTACCTCTCATTTTCCTT TCTGTTTGTTACAGGGTTGCAACTGTCGGGTCTTGATGCCAGAAGCTTTACCTCTCATTTTCCTT A T KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40386322..40386450 26863196 MeRIP-seq:(Medium) rs367716458 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_8803788,Human_RBP_ID_25135637 RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889 111941 RMVar_ID_111941 Human_SNP_ID_823626262 m1A Human chr15 - 90265726 90265726 90265726 CGGCGCAAACGCGCCCGCCCAGCAAGAGACTCAGGGTAACCGCCATGTCGACGCAAACCAGCCTT CGGCGCAAACGCGCCCGCCCAGCAAGAGACTCGGGGTAACCGCCATGTCGACGCAAACCAGCCTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr15:90265676..90265875;chr15:90265676..90265927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111942 RMVar_ID_111942 Human_SNP_ID_823646562 m1A Human chr15 - 64387906 64387906 64387906 GCCGAAAGTCTTCCGCAACTGCTGGGTGCACCAGTGCACCAGCGGCTCCCCGGACACCGCCCCAG GCCGAAAGTCTTCCGCAACTGCTGGGTGCACCGGTGCACCAGCGGCTCCCCGGACACCGCCCCAG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64387851..64393353 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 111943 RMVar_ID_111943 Human_SNP_ID_823651912 m1A Human chr15 + 40751561 40751561 40751561 TTCGCCGCCGAGCCACTCTCTGGTTCTCTTCCATGTGGCATCTGGAAAGCAGGCCCCATCCCGAA TTCGCCGCCGAGCCACTCTCTGGTTCTCTTCCGTGTGGCATCTGGAAAGCAGGCCCCATCCCGAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40751512..40752125 26863196 MeRIP-seq:(Medium) rs1165844191 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 111944 RMVar_ID_111944 Human_SNP_ID_823683130 m1A Human chr15 + 40386313 40386313 40386313 TCGAATGGGGCTCTGTTTGTTACAGGGTTGCAACTGTCGGGTCATGATGCCAGAAGCTTTACCTC TCGAATGGGGCTCTGTTTGTTACAGGGTTGCAGCTGTCGGGTCATGATGCCAGAAGCTTTACCTC A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40386310..40386475 26863196 MeRIP-seq:(Medium) rs199948606 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3473476,Human_RBP_ID_8803788 RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889 111945 RMVar_ID_111945 Human_SNP_ID_823687959 m1A Human chr15 - 44711575 44711575 44711575 TAGCCTCCAGGCCAGAAAGAGAGAGTAGCGCGAGCACAGCTAAGGCCACGGAGCGAGACATCTCG TAGCCTCCAGGCCAGAAAGAGAGAGTAGCGCGCGCACAGCTAAGGCCACGGAGCGAGACATCTCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:44711526..44711799;chr15:44711526..44711575;chr15:44711526..44711862;chr15:44711501..44711684;chr15:44711526..44711670 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 spleen diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 7 spleen,haematopoietic and lymphoid tissue 111946 RMVar_ID_111946 Human_SNP_ID_823695353 m1A Human chr15 + 74022902 74022902 74022902 CGCGCTCCTTGACAGCAGCCACAGTGAGCTCAAGTGCGACATCAGCGCAGAGATCCAGCAGCGAC CGCGCTCCTTGACAGCAGCCACAGTGAGCTCATGTGCGACATCAGCGCAGAGATCCAGCAGCGAC A T PML Ensembl:ENSG00000140464 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74022852..74022924 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 14 lung Human_RBP_ID_1001985,Human_RBP_ID_9283310,Human_RBP_ID_22496746 Human_Splice_Rec_1624366,Human_Splice_Rec_1624380,Human_Splice_Rec_1624396,Human_Splice_Rec_1624404,Human_Splice_Rec_1624418,Human_Splice_Rec_1624430,Human_Splice_Rec_1624444,Human_Splice_Rec_1624458,Human_Splice_Rec_1624472,Human_Splice_Rec_1624480,Human_Splice_Rec_1624494,Human_Splice_Rec_1624506,Human_Splice_Rec_1624518,Human_Splice_Rec_1624528,Human_Splice_Rec_1624534 RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 111947 RMVar_ID_111947 Human_SNP_ID_823711584 m1A Human chr15 + 78274242 78274242 78274242 GAAGGGATCGGTGGAGAAGTGCCCGCTGTGCAAGGGGCGGGGGATGCAGATCCACATCCAGCAGA GAAGGGATCGGTGGAGAAGTGCCCGCTGTGCAGGGGGCGGGGGATGCAGATCCACATCCAGCAGA A G DNAJA4 Ensembl:ENSG00000140403 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:78273198..78274400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_Splice_Rec_1631792,Human_Splice_Rec_1631810,Human_Splice_Rec_1631824,Human_Splice_Rec_1631832,Human_Splice_Rec_1631846,Human_Splice_Rec_1631858,Human_Splice_Rec_1631868,Human_Splice_Rec_1631878,Human_Splice_Rec_1631888 RMVar_hsa_circ_20705,RMVar_hsa_circ_23270,RMVar_hsa_circ_269169,RMVar_hsa_circ_356113 111948 RMVar_ID_111948 Human_SNP_ID_823723539 m1A Human chr15 - 75354721 75354721 75354721 TGGAGGCTGGTCCCCTCAGGCCGCTGGGTTGCAGTCCTCTTAGGAAGGTCTCTCTTTGCCCTTCG TGGAGGCTGGTCCCCTCAGGCCGCTGGGTTGCTGTCCTCTTAGGAAGGTCTCTCTTTGCCCTTCG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75354672..75354968 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_1364207 111949 RMVar_ID_111949 Human_SNP_ID_823725579 m1A Human chr15 + 66356501 66356501 66356501 GCCTCTCCAGGCCGGGTCAGGTCGACCCCCCAACCTCCTGACCCCCTTCCTGCGACAATTAGGCT GCCTCTCCAGGCCGGGTCAGGTCGACCCCCCAGCCTCCTGACCCCCTTCCTGCGACAATTAGGCT A G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:66356490..66356675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111950 RMVar_ID_111950 Human_SNP_ID_823744845 m1A Human chr15 - 57591983 57591983 57591983 GCGGGCTGGACGCCGGCGTTCCTCCCGGGCAGAATAAGCGTGCGGGGCCCGCCCTGCGCGGGGGC GCGGGCTGGACGCCGGCGTTCCTCCCGGGCAGGATAAGCGTGCGGGGCCCGCCCTGCGCGGGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:57591948..57592054 26863196 MeRIP-seq:(Medium) rs1690328 Functional Loss SNV ICGC 33..33 33 COCA 4 - 111951 RMVar_ID_111951 Human_SNP_ID_823747328 m1A Human chr15 - 24978474 24978474 24978474 TCTACACAATTTCACAAGACGCATTGCAGGGGAAAAAGTGACTGAGATGGATCAACAGTATGCTA TCTACACAATTTCACAAGACGCATTGCAGGGGGAAAAGTGACTGAGATGGATCAACAGTATGCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:24978163..24979541 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 10 lung 111952 RMVar_ID_111952 Human_SNP_ID_823750527 m1A Human chr15 - 72200603 72200602 72200603 GATACCGCCCACGTGCCCCCATCATTGCTGTGACCCGGAATCCCCAGACAGCTCGTCAGGCCCAC GATACCGCCCACGTGCCCCCATCATTGCTGTG_CCCGGAATCCCCAGACAGCTCGTCAGGCCCAC GT G PKM Ensembl:ENSG00000067225 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:72200553..72200677 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BRCA 1 - Human_RBP_ID_41146,Human_RBP_ID_462832,Human_RBP_ID_1001899,Human_RBP_ID_1507833,Human_RBP_ID_1833417,Human_RBP_ID_3481647,Human_RBP_ID_6458257,Human_RBP_ID_8421877,Human_RBP_ID_8801989,Human_RBP_ID_17250963,Human_RBP_ID_18667384,Human_RBP_ID_22046298,Human_RBP_ID_22439846,Human_RBP_ID_22532625,Human_RBP_ID_22759282,Human_RBP_ID_22799173,Human_RBP_ID_27233682 Human_Splice_Rec_1621758,Human_Splice_Rec_1621774,Human_Splice_Rec_1621790,Human_Splice_Rec_1621804,Human_Splice_Rec_1621818,Human_Splice_Rec_1621834,Human_Splice_Rec_1621842,Human_Splice_Rec_1621860,Human_Splice_Rec_1621878,Human_Splice_Rec_1621894,Human_Splice_Rec_1621910 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_101849,RMVar_hsa_circ_103902,RMVar_hsa_circ_100071,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_93888,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173687,RMVar_hsa_circ_173689,RMVar_hsa_circ_173688,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173691 111953 RMVar_ID_111953 Human_SNP_ID_823757744 m1A Human chr15 - 66435202 66435202 66435202 TCTGGCCATGACCAGGCCAGAAGGCTTGTGGGAGACCTTGAACACCACACCGCCATTGCCAGCCC TCTGGCCATGACCAGGCCAGAAGGCTTGTGGGCGACCTTGAACACCACACCGCCATTGCCAGCCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:66435151..66444746 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 111954 RMVar_ID_111954 Human_SNP_ID_823788954 m1A Human chr15 + 70667731 70667731 70667731 CTCGCACTCCTCAAAGCTGACAATTGGGGCGTATTTTACCTTAATGCATTCTTGTATTGTGTCGA CTCGCACTCCTCAAAGCTGACAATTGGGGCGTCTTTTACCTTAATGCATTCTTGTATTGTGTCGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:70667681..70667769 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 111955 RMVar_ID_111955 Human_SNP_ID_823794961 m1A Human chr15 + 64691551 64691551 64691551 GCACCACAGAGGCCCTGGAACAATGTGCCTGCAGCACTGGAGCTGGGGACAGTTACTCAAAGGCA GCACCACAGAGGCCCTGGAACAATGTGCCTGCGGCACTGGAGCTGGGGACAGTTACTCAAAGGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:64691501..64691644 26863196 MeRIP-seq:(Medium) rs907476653 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 3 stomach 111956 RMVar_ID_111956 Human_SNP_ID_823814776 m1A Human chr15 - 70058236 70058236 70058236 GCTCAAGTCCAACACACCAACCCCAAGGAACGACGCCCCAACTCCAGGCACCAGCACGACCCCAG GCTCAAGTCCAACACACCAACCCCAAGGAACGGCGCCCCAACTCCAGGCACCAGCACGACCCCAG T C TLE3 Ensembl:ENSG00000140332 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:70058151..70058250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 15 large intestine Human_RBP_ID_9284107,Human_RBP_ID_17250915,Human_RBP_ID_27436574 Human_Splice_Rec_1619528,Human_Splice_Rec_1619529,Human_Splice_Rec_1619566,Human_Splice_Rec_1619567,Human_Splice_Rec_1619600,Human_Splice_Rec_1619601,Human_Splice_Rec_1619638,Human_Splice_Rec_1619639,Human_Splice_Rec_1619676,Human_Splice_Rec_1619677,Human_Splice_Rec_1619714,Human_Splice_Rec_1619715,Human_Splice_Rec_1619752,Human_Splice_Rec_1619753,Human_Splice_Rec_1619790,Human_Splice_Rec_1619791,Human_Splice_Rec_1619826,Human_Splice_Rec_1619827,Human_Splice_Rec_1619862,Human_Splice_Rec_1619863,Human_Splice_Rec_1619900,Human_Splice_Rec_1619901,Human_Splice_Rec_1619938,Human_Splice_Rec_1619939,Human_Splice_Rec_1619974,Human_Splice_Rec_1619975,Human_Splice_Rec_1620010,Human_Splice_Rec_1620011,Human_Splice_Rec_1620048,Human_Splice_Rec_1620049,Human_Splice_Rec_1620102,Human_Splice_Rec_1620103,Human_Splice_Rec_1620140,Human_Splice_Rec_1620141,Human_Splice_Rec_1620162 RMVar_hsa_circ_40774,RMVar_hsa_circ_33823 111957 RMVar_ID_111957 Human_SNP_ID_823838141 m1A Human chr15 + 43370975 43370975 43370975 GGCCAGCCTCACCCACTCGGGGTCCGACCCTGACCCCGGCCCCGGCCCCGGCCCCGGCCCCGGCT GGCCAGCCTCACCCACTCGGGGTCCGACCCTGGCCCCGGCCCCGGCCCCGGCCCCGGCCCCGGCT A G TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:43370857..43371027 26863196 MeRIP-seq:(Medium) rs3840834 Functional Loss SNV ICGC 33..33 33 MELA 1 - 111958 RMVar_ID_111958 Human_SNP_ID_823861521 m1A Human chr15 + 41285231 41285230 41285231 TGTTTTTTTGTCTTTGTCTCATCCAGGAGAAGAAAAAAAATATCGGCCAGAGGAGAGGAACTAAC TGTTTTTTTGTCTTTGTCTCATCCAGGAGAAG_AAAAAAATATCGGCCAGAGGAGAGGAACTAAC GA G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:41285226..41285275 26863410 MeRIP-seq:(Medium) rs1230954315 Functional Loss DEL ICGC 33..33 33 STAD 2 - Human_RBP_ID_886346,Human_RBP_ID_1511667,Human_RBP_ID_4342590,Human_RBP_ID_5180484,Human_RBP_ID_5568898,Human_RBP_ID_5646575,Human_RBP_ID_8183611,Human_RBP_ID_9345360,Human_RBP_ID_9370735,Human_RBP_ID_17859854,Human_RBP_ID_22048091,Human_RBP_ID_22540800,Human_RBP_ID_25183695,Human_RBP_ID_26326525,Human_RBP_ID_26808819,Human_RBP_ID_27809351 Human_Splice_Rec_1586362,Human_Splice_Rec_1586366,Human_Splice_Rec_1586372,Human_Splice_Rec_1586378,Human_Splice_Rec_1586384,Human_Splice_Rec_1586390,Human_Splice_Rec_1586398,Human_Splice_Rec_1586400,Human_Splice_Rec_1586406,Human_Splice_Rec_1586412,Human_Splice_Rec_1586420,Human_Splice_Rec_1586448 Human_miRNA_ID_2364488,Human_miRNA_ID_2364489 RMVar_hsa_circ_121853,RMVar_hsa_circ_171045,RMVar_hsa_circ_118405,RMVar_hsa_circ_171044 111959 RMVar_ID_111959 Human_SNP_ID_823869135 m1A Human chr15 + 39934258 39934258 39934258 GGCCGGGACGAGCCTCCGGAGAGCTACCCGCAACGACAGGACCACGAGCTACAGGCCCTGGAGGC GGCCGGGACGAGCCTCCGGAGAGCTACCCGCAGCGACAGGACCACGAGCTACAGGCCCTGGAGGC A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr15:39934173..39934325;chr15:39934147..39934325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LIHC 1 - Human_RBP_ID_4342554,Human_RBP_ID_9283581 Human_Splice_Rec_1583067,Human_Splice_Rec_1583143,Human_Splice_Rec_1583163 RMVar_hsa_circ_105405,RMVar_hsa_circ_170835 111960 RMVar_ID_111960 Human_SNP_ID_823899102 m1A Human chr15 - 75364647 75364647 75364647 CCCCATCTTTGTAGCCTCACTCTCTATGTGGAAGTAGCCTGCAATGGGCTCCTGGGGGCCGGGAA CCCCATCTTTGTAGCCTCACTCTCTATGTGGATGTAGCCTGCAATGGGCTCCTGGGGGCCGGGAA T A MAN2C1 Ensembl:ENSG00000140400 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:75363289..75364649 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_884409,Human_RBP_ID_3946602,Human_RBP_ID_5523456,Human_RBP_ID_18981711 Human_Splice_Rec_1628176,Human_Splice_Rec_1628224,Human_Splice_Rec_1628272,Human_Splice_Rec_1628316,Human_Splice_Rec_1628436,Human_Splice_Rec_1628560,Human_Splice_Rec_1628572,Human_Splice_Rec_1628604,Human_Splice_Rec_1628618,Human_Splice_Rec_1628626,Human_Splice_Rec_1628636,Human_Splice_Rec_1628646,Human_Splice_Rec_1628654,Human_Splice_Rec_1628664 RMVar_hsa_circ_86117,RMVar_hsa_circ_173935,RMVar_hsa_circ_66404 111961 RMVar_ID_111961 Human_SNP_ID_823906377 m1A Human chr15 + 66293633 66293633 66293633 TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGACCTTCCAGGGCCGCACGCTGCGGATCGTGCGC TGCAGAAGCGGGAGAAGGTGCTGCTGCTGAGGTCCTTCCAGGGCCGCACGCTGCGGATCGTGCGC A T DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66293584..66293680 26863196 MeRIP-seq:(Medium) rs902503635 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 haematopoietic and lymphoid tissue Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 111962 RMVar_ID_111962 Human_SNP_ID_823926476 m1A Human chr15 + 66703337 66703337 66703337 GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCAGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG GTCGTGTGGTCCCCGACCGGGAGGAAGGCGGCGGCGGCGGCGGCGGTGGCGGCGACGAGGATGGG A G SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66703226..66703500 26863196 MeRIP-seq:(Medium) rs374058045 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_3489128,Human_RBP_ID_18481000,Human_RBP_ID_22192621,Human_RBP_ID_22712033 111963 RMVar_ID_111963 Human_SNP_ID_823931436 m1A Human chr15 - 44715552 44715552 44715552 TGAAAGACAAGTCTGAATGCTCCACTTTTTCAATTCTCTCTCCATTCTTCAGTAAGTCAACTTCA TGAAAGACAAGTCTGAATGCTCCACTTTTTCATTTCTCTCTCCATTCTTCAGTAAGTCAACTTCA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:44715401..44715700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 111964 RMVar_ID_111964 Human_SNP_ID_823941057 m1A Human chr15 - 58883782 58883782 58883782 AGTGACTTTTCATATGCTATTCTTTTAGCACTATCCTGAGGAGCGACATGTGGTTGAACGCCATG AGTGACTTTTCATATGCTATTCTTTTAGCACTTTCCTGAGGAGCGACATGTGGTTGAACGCCATG T A SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:58883626..58883841 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_232099,Human_RBP_ID_885589,Human_RBP_ID_2447440,Human_RBP_ID_8803856,Human_RBP_ID_9283652,Human_RBP_ID_9371633,Human_RBP_ID_18982275,Human_RBP_ID_19068257,Human_RBP_ID_24544087,Human_RBP_ID_26326766,Human_RBP_ID_27809606 Human_Splice_Rec_1607918,Human_Splice_Rec_1607942,Human_Splice_Rec_1607946,Human_Splice_Rec_1607984,Human_Splice_Rec_1607988,Human_Splice_Rec_1608024,Human_Splice_Rec_1608032 RMVar_hsa_circ_350062,RMVar_hsa_circ_366512,RMVar_hsa_circ_376047,RMVar_hsa_circ_358913,RMVar_hsa_circ_94624,RMVar_hsa_circ_126659,RMVar_hsa_circ_335055,RMVar_hsa_circ_124260,RMVar_hsa_circ_172432,RMVar_hsa_circ_63224,RMVar_hsa_circ_73676,RMVar_hsa_circ_172433,RMVar_hsa_circ_172434,RMVar_hsa_circ_172430,RMVar_hsa_circ_172431 111965 RMVar_ID_111965 Human_SNP_ID_823947433 m1A Human chr15 + 66293673 66293673 66293673 GGGCCGCACGCTGCGGATCGTGCGCGAGCACTACCTGCGGCCCTGCGTGCCCTGCCACAGCCCGC GGGCCGCACGCTGCGGATCGTGCGCGAGCACTGCCTGCGGCCCTGCGTGCCCTGCCACAGCCCGC A G DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:66293624..66293689 26863196 MeRIP-seq:(Medium) rs1162761758 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_4342341,Human_RBP_ID_18982342,Human_RBP_ID_23113803 Human_Splice_Rec_1615779,Human_Splice_Rec_1615801,Human_Splice_Rec_1615833,Human_Splice_Rec_1615855 111966 RMVar_ID_111966 Human_SNP_ID_823956207 m1A Human chr15 + 23565761 23565761 23565761 TAAAGAAAAAATACCGGAGAGGTTCTGGCACCATTTCGGGGTGCCAAAGCAGCCATGGAAGAGCC TAAAGAAAAAATACCGGAGAGGTTCTGGCACCGTTTCGGGGTGCCAAAGCAGCCATGGAAGAGCC A G MKRN3 Ensembl:ENSG00000179455 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:23565710..23565852 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_17858088 111967 RMVar_ID_111967 Human_SNP_ID_823956733 m1A Human chr15 + 60478039 60478039 60478039 ACAGTTCACAGCTGCCTGGCTGCGAAGGCTCCAAGAGGCAGGATCCCTCCAGAACTTACTCAGCT ACAGTTCACAGCTGCCTGGCTGCGAAGGCTCCCAGAGGCAGGATCCCTCCAGAACTTACTCAGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:60477988..60478115 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 111968 RMVar_ID_111968 Human_SNP_ID_823973262 m1A Human chr15 - 85568446 85568446 85568446 AACTGTAAATGTGCATTCCTCAAAGACACCTCATCATCCAGGGATTCCAGACTATCCAAAACCCA AACTGTAAATGTGCATTCCTCAAAGACACCTCTTCATCCAGGGATTCCAGACTATCCAAAACCCA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:85568348..85568532 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 111969 RMVar_ID_111969 Human_SNP_ID_824001986 m1A Human chr15 + 39934233 39934233 39934233 TGGGGGCCGTGGGGCCCCCGGGCGCGGCCGGGACGAGCCTCCGGAGAGCTACCCGCAACGACAGG TGGGGGCCGTGGGGCCCCCGGGCGCGGCCGGGGCGAGCCTCCGGAGAGCTACCCGCAACGACAGG A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:39934183..39934277;chr15:39934183..39934270 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney Human_RBP_ID_232049,Human_RBP_ID_4318824,Human_RBP_ID_8803778,Human_RBP_ID_9283581,Human_RBP_ID_9324215,Human_RBP_ID_27810066 RMVar_hsa_circ_105405,RMVar_hsa_circ_170835 111970 RMVar_ID_111970 Human_SNP_ID_824022986 m1A Human chr15 - 44289106 44289106 44289106 AGGAGATGCTCCAGTAGTTGAAGGCGAGGACGACGATCACCACCAGCAGCACCACCAGCACGAGA AGGAGATGCTCCAGTAGTTGAAGGCGAGGACGGCGATCACCACCAGCAGCACCACCAGCACGAGA T C lnc-FRMD5-1,lnc-FRMD5-1:2 RNACentral:URS00008C113C,RNACentral:URS00008BBD75 lincRNA,lincRNA exon,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:44289019..44289187 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 111971 RMVar_ID_111971 Human_SNP_ID_824039564 m1A Human chr15 - 43746601 43746601 43746601 CCGTGAGTTCTAGCACGTCGGAGGCAGCGGCGAGGCGGGCCGCGGCAAGAAGCAGCGCCACACCC CCGTGAGTTCTAGCACGTCGGAGGCAGCGGCGTGGCGGGCCGCGGCAAGAAGCAGCGCCACACCC T A CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:43746426..43746725 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_5567364 Human_Splice_Rec_1594541 111972 RMVar_ID_111972 Human_SNP_ID_824045667 m1A Human chr15 - 51851055 51851055 51851055 TGACTGTGTCTCTCTGGAACTCCTCTGGCAAAACCCCACATCTGGTTAAAACTAACTCTTCCGGC TGACTGTGTCTCTCTGGAACTCCTCTGGCAAACCCCCACATCTGGTTAAAACTAACTCTTCCGGC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:51851053..51851137 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 111973 RMVar_ID_111973 Human_SNP_ID_824046616 m1A Human chr15 - 43792378 43792378 43792378 GCAAGGAGAAGGGGGCTCGGTGCTCACGGGTCATGGCGACGGCAGCGGCTCCAACCTGCCTCCGT GCAAGGAGAAGGGGGCTCGGTGCTCACGGGTCGTGGCGACGGCAGCGGCTCCAACCTGCCTCCGT T C AC018512.1 Ensembl:ENSG00000262560 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:43792326..43792499 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 9 prostate 111974 RMVar_ID_111974 Human_SNP_ID_824057571 m1A Human chr15 - 90388327 90388327 90388327 CTCGTCTGCGGCGGACATGGCGGACGAGCCCGAGTCTCTGCTGAGGAAGCCGTGAAACCTTGGAG CTCGTCTGCGGCGGACATGGCGGACGAGCCCGTGTCTCTGCTGAGGAAGCCGTGAAACCTTGGAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:90388276..90388456 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_23127709 111975 RMVar_ID_111975 Human_SNP_ID_824058215 m1A Human chr15 - 45200418 45200418 45200418 TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCACGGCATTGTGAGGACAATGGCACGGCAAGGGG TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCGCGGCATTGTGAGGACAATGGCACGGCAAGGGG T C SHF,AC051619.7 Ensembl:ENSG00000138606,Ensembl:ENSG00000260035 Protein coding,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:45200376..45200514 26863196 MeRIP-seq:(Medium) rs917822614 Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_42941,Human_RBP_ID_232454,Human_RBP_ID_759457,Human_RBP_ID_814632,Human_RBP_ID_1504982,Human_RBP_ID_1829906,Human_RBP_ID_3475187,Human_RBP_ID_4343758,Human_RBP_ID_5087817,Human_RBP_ID_5180441,Human_RBP_ID_5258953,Human_RBP_ID_5646558,Human_RBP_ID_6429741,Human_RBP_ID_8183641,Human_RBP_ID_8250989,Human_RBP_ID_8417355,Human_RBP_ID_8800338,Human_RBP_ID_12518933,Human_RBP_ID_17077271,Human_RBP_ID_18480899,Human_RBP_ID_18545367,Human_RBP_ID_18663335,Human_RBP_ID_20025571,Human_RBP_ID_22531515,Human_RBP_ID_22798868,Human_RBP_ID_23113772,Human_RBP_ID_23127380,Human_RBP_ID_23653131,Human_RBP_ID_24473636,Human_RBP_ID_24531025,Human_RBP_ID_25184368,Human_RBP_ID_27651144 Human_miRNA_ID_3164675 111976 RMVar_ID_111976 Human_SNP_ID_824058218 m1A Human chr15 - 45200418 45200418 45200418 TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCACGGCATTGTGAGGACAATGGCACGGCAAGGGG TGGCCGCAGCAACCTCGGTTCGAATCCGAGTCTCGGCATTGTGAGGACAATGGCACGGCAAGGGG T A SHF,AC051619.7 Ensembl:ENSG00000138606,Ensembl:ENSG00000260035 Protein coding,lincRNA intron,exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:45200376..45200514 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_42941,Human_RBP_ID_232454,Human_RBP_ID_759457,Human_RBP_ID_814632,Human_RBP_ID_1504982,Human_RBP_ID_1829906,Human_RBP_ID_3475187,Human_RBP_ID_4343758,Human_RBP_ID_5087817,Human_RBP_ID_5180441,Human_RBP_ID_5258953,Human_RBP_ID_5646558,Human_RBP_ID_6429741,Human_RBP_ID_8183641,Human_RBP_ID_8250989,Human_RBP_ID_8417355,Human_RBP_ID_8800338,Human_RBP_ID_12518933,Human_RBP_ID_17077271,Human_RBP_ID_18480899,Human_RBP_ID_18545367,Human_RBP_ID_18663335,Human_RBP_ID_20025571,Human_RBP_ID_22531515,Human_RBP_ID_22798868,Human_RBP_ID_23113772,Human_RBP_ID_23127380,Human_RBP_ID_23653131,Human_RBP_ID_24473636,Human_RBP_ID_24531025,Human_RBP_ID_25184368,Human_RBP_ID_27651144 Human_miRNA_ID_3164675 111977 RMVar_ID_111977 Human_SNP_ID_824072322 m1A Human chr15 - 34969639 34969639 34969639 TTGCCGCTGCCCAGAGCGGTCCTTTAGTTTCCACTGGAGTGGAGGGAAGAGTGCTGCCATGGCAG TTGCCGCTGCCCAGAGCGGTCCTTTAGTTTCCGCTGGAGTGGAGGGAAGAGTGCTGCCATGGCAG T C AQR Ensembl:ENSG00000021776 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34969588..34969689 32194978 MeRIP-seq:(Medium) rs759283394 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_41117,Human_RBP_ID_4318338,Human_RBP_ID_8803771,Human_RBP_ID_9283576,Human_RBP_ID_9370668,Human_RBP_ID_18661592,Human_RBP_ID_22934639,Human_RBP_ID_26327979 RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_82898,RMVar_hsa_circ_170616 111978 RMVar_ID_111978 Human_SNP_ID_824088045 m1A Human chr15 - 90974636 90974636 90974636 GTGAATGGGCAGAAATTCATGGAGTATGTGGCAGAACAATGGGAGATGCATCGATTGGAGAAAGA GTGAATGGGCAGAAATTCATGGAGTATGTGGCGGAACAATGGGAGATGCATCGATTGGAGAAAGA T C AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr15:90974539..90974678;chr15:90974532..90974675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_42899,Human_RBP_ID_232430,Human_RBP_ID_1130174,Human_RBP_ID_1511040,Human_RBP_ID_1837135,Human_RBP_ID_3487604,Human_RBP_ID_5566862,Human_RBP_ID_6480266,Human_RBP_ID_8426106,Human_RBP_ID_8803370,Human_RBP_ID_9371282,Human_RBP_ID_12639767,Human_RBP_ID_22933953,Human_RBP_ID_23113780,Human_RBP_ID_23674641,Human_RBP_ID_24544143,Human_RBP_ID_26327077,Human_RBP_ID_27809891 Human_Splice_Rec_1645878,Human_Splice_Rec_1645879,Human_Splice_Rec_1645910,Human_Splice_Rec_1645911,Human_Splice_Rec_1645920,Human_Splice_Rec_1645921,Human_Splice_Rec_1645952,Human_Splice_Rec_1645953,Human_Splice_Rec_1645966,Human_Splice_Rec_1645967,Human_Splice_Rec_1645972,Human_Splice_Rec_1645973,Human_Splice_Rec_1645980,Human_Splice_Rec_1646100,Human_Splice_Rec_1646101,Human_Splice_Rec_1646166 Human_miRNA_ID_2214646 RMVar_hsa_circ_75163,RMVar_hsa_circ_49308,RMVar_hsa_circ_106428,RMVar_hsa_circ_114313,RMVar_hsa_circ_121413,RMVar_hsa_circ_109536,RMVar_hsa_circ_90798,RMVar_hsa_circ_174908,RMVar_hsa_circ_174910,RMVar_hsa_circ_174911,RMVar_hsa_circ_174912,RMVar_hsa_circ_174909,RMVar_hsa_circ_114358,RMVar_hsa_circ_116418,RMVar_hsa_circ_375970,RMVar_hsa_circ_99176,RMVar_hsa_circ_174915,RMVar_hsa_circ_174916,RMVar_hsa_circ_174917,RMVar_hsa_circ_174914,RMVar_hsa_circ_61093,RMVar_hsa_circ_104298,RMVar_hsa_circ_30689,RMVar_hsa_circ_370843,RMVar_hsa_circ_174918,RMVar_hsa_circ_174919,RMVar_hsa_circ_98695,RMVar_hsa_circ_174920,RMVar_hsa_circ_62368,RMVar_hsa_circ_174921,RMVar_hsa_circ_81400 111979 RMVar_ID_111979 Human_SNP_ID_824096451 m1A Human chr15 - 34793545 34793545 34793545 TCTCATAGGGAGTTATGGTGGGTATGGGTCAGAAGGACTCCTACGTAGGTGATGAAGCCCAGAGC TCTCATAGGGAGTTATGGTGGGTATGGGTCAGCAGGACTCCTACGTAGGTGATGAAGCCCAGAGC T G ACTC1 Ensembl:ENSG00000159251 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:34793429..34793624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_RBP_ID_26748578 Human_Splice_Rec_1581108,Human_Splice_Rec_1581118,Human_Splice_Rec_1581130,Human_Splice_Rec_1581148 RMVar_hsa_circ_107513,RMVar_hsa_circ_170553 111980 RMVar_ID_111980 Human_SNP_ID_824109558 m1A Human chr15 - 78878149 78878131 78878149 TTTCTTCTCATATATAAAAAGATTAACATCTTAGAGAGTCATCACACTTTTATTAAGGTATTCCT TTTCTTCTCATATATAAAAAGATTAACATCTT__________________TATTAAGGTATTCCT AAAAGTGTGATGACTCTCT A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:78878146..78878314 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..50 33 LICA 1 - 111981 RMVar_ID_111981 Human_SNP_ID_824133247 m1A Human chr15 + 65879673 65879673 65879673 ACAAGACTGAACTTTTGTGTCTCCCCTCAGAAAAGAATGGTTTGTCATTCATTGAAACTTCGGCC ACAAGACTGAACTTTTGTGTCTCCCCTCAGAACAGAATGGTTTGTCATTCATTGAAACTTCGGCC A C RAB11A Ensembl:ENSG00000103769 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_885690,Human_RBP_ID_1506621,Human_RBP_ID_1832154,Human_RBP_ID_9345470,Human_RBP_ID_22650771,Human_RBP_ID_22758871,Human_RBP_ID_23661349 Human_Splice_Rec_1615404,Human_Splice_Rec_1615405,Human_Splice_Rec_1615419,Human_Splice_Rec_1615426,Human_Splice_Rec_1615427,Human_Splice_Rec_1615434,Human_Splice_Rec_1615435,Human_Splice_Rec_1615442,Human_Splice_Rec_1615443 RMVar_hsa_circ_310464,RMVar_hsa_circ_173276,RMVar_hsa_circ_173278 111982 RMVar_ID_111982 Human_SNP_ID_824144720 m1A Human chr15 + 66781297 66781297 66781297 GCACCCCATCTTCGTCAACTCCCCGACGCTGGACGCGCCCGGCGGCCGCGCCCTGGTCGTGCGCA GCACCCCATCTTCGTCAACTCCCCGACGCTGGTCGCGCCCGGCGGCCGCGCCCTGGTCGTGCGCA A T SMAD6 Ensembl:ENSG00000137834 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:66781151..66781550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_18189577,Human_RBP_ID_26809037 RMVar_hsa_circ_98331,RMVar_hsa_circ_173347 111983 RMVar_ID_111983 Human_SNP_ID_824151818 m1A Human chr15 + 85741278 85741278 85741278 TGAGTGGGAAGCTCGTGAGAGGGAGCTGCGGGAGCGGGAGGCCCTCCTGGCCCAGCGCGAGGAGG TGAGTGGGAAGCTCGTGAGAGGGAGCTGCGGGGGCGGGAGGCCCTCCTGGCCCAGCGCGAGGAGG A G AKAP13 Ensembl:ENSG00000170776 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:85741227..85741363 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_43404 RMVar_hsa_circ_58355,RMVar_hsa_circ_57898,RMVar_hsa_circ_356246,RMVar_hsa_circ_58374,RMVar_hsa_circ_348997 111984 RMVar_ID_111984 Human_SNP_ID_824155917 m1A Human chr15 - 34341990 34341990 34341990 CATCAAGAAACGCTTCAAGGTGCTCATGACCCAGCAACCGCGCCCTGTCCTCTGAGGGTCCCTTA CATCAAGAAACGCTTCAAGGTGCTCATGACCCTGCAACCGCGCCCTGTCCTCTGAGGGTCCCTTA T A NOP10 Ensembl:ENSG00000182117 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34341843..34342153 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_456038,Human_RBP_ID_17187697,Human_RBP_ID_22532597,Human_RBP_ID_26930467,Human_RBP_ID_27230880 Human_Splice_Rec_1580622 Human_miRNA_ID_2917522 RMVar_hsa_circ_170545,RMVar_hsa_circ_102468,RMVar_hsa_circ_118453,RMVar_hsa_circ_170546 111985 RMVar_ID_111985 Human_SNP_ID_824172205 m1A Human chr15 + 52568952 52568952 52568952 GGAAAAGATGCAATTAGCGGGTGGCCGAGGCCACCCGGCCGCCGCCCGTCCCAGCTCTCCCAGGG GGAAAAGATGCAATTAGCGGGTGGCCGAGGCCCCCCGGCCGCCGCCCGTCCCAGCTCTCCCAGGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:52568826..52569025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 10 pancreas 111986 RMVar_ID_111986 Human_SNP_ID_824182217 m1A Human chr15 - 44711599 44711599 44711599 AGGGTAGGAGAGACTCACGCTGGATAGCCTCCAGGCCAGAAAGAGAGAGTAGCGCGAGCACAGCT AGGGTAGGAGAGACTCACGCTGGATAGCCTCCCGGCCAGAAAGAGAGAGTAGCGCGAGCACAGCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T,ALKBH3 KO;HTR8/Svneo,Normoxia chr15:44711501..44711650;chr15:44711526..44711625 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 3 head and neck 111987 RMVar_ID_111987 Human_SNP_ID_824225390 m1A Human chr15 - 40458751 40458751 40458751 CACTGGATGGGGCCGGGCTGGGGGGCTTGGGCAGGTCAGGCGGTAGCTCATCAGCCTCATCTGCA CACTGGATGGGGCCGGGCTGGGGGGCTTGGGCCGGTCAGGCGGTAGCTCATCAGCCTCATCTGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:40458700..40458845 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 3 haematopoietic and lymphoid tissue 111988 RMVar_ID_111988 Human_SNP_ID_824226266 m1A Human chr15 - 43441559 43441558 43441559 TTATTCAGAGCCTGCAACTGGTGAAAGAAAAAATGGATCTACTGCTGTTGCTGAGTCTGTTGCCA TTATTCAGAGCCTGCAACTGGTGAAAGAAAAA_TGGATCTACTGCTGTTGCTGAGTCTGTTGCCA AT A TP53BP1 Ensembl:ENSG00000067369 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43441523..43446802 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 PRAD,STAD,COCA,HNSC,UCEC 7 - Human_RBP_ID_885007,Human_RBP_ID_3945455,Human_RBP_ID_8800187,Human_RBP_ID_25139753 Human_Splice_Rec_1592694,Human_Splice_Rec_1592695,Human_Splice_Rec_1592748,Human_Splice_Rec_1592749,Human_Splice_Rec_1592794,Human_Splice_Rec_1592795,Human_Splice_Rec_1592848,Human_Splice_Rec_1592849,Human_Splice_Rec_1592900,Human_Splice_Rec_1592901,Human_Splice_Rec_1592968,Human_Splice_Rec_1592969,Human_Splice_Rec_1593024,Human_Splice_Rec_1593025,Human_Splice_Rec_1593030 Human_miRNA_ID_1044800 RMVar_hsa_circ_107044,RMVar_hsa_circ_171466,RMVar_hsa_circ_104974,RMVar_hsa_circ_127231,RMVar_hsa_circ_171467,RMVar_hsa_circ_889,RMVar_hsa_circ_171468,RMVar_hsa_circ_53912,RMVar_hsa_circ_86730,RMVar_hsa_circ_171470,RMVar_hsa_circ_126188,RMVar_hsa_circ_13589,RMVar_hsa_circ_16999,RMVar_hsa_circ_24634,RMVar_hsa_circ_171472,RMVar_hsa_circ_76379,RMVar_hsa_circ_171473,RMVar_hsa_circ_171471,RMVar_hsa_circ_34296,RMVar_hsa_circ_93271,RMVar_hsa_circ_171476,RMVar_hsa_circ_171477,RMVar_hsa_circ_266969,RMVar_hsa_circ_310538,RMVar_hsa_circ_319384,RMVar_hsa_circ_271743,RMVar_hsa_circ_171480,RMVar_hsa_circ_171481,RMVar_hsa_circ_372782,RMVar_hsa_circ_171484,RMVar_hsa_circ_84840,RMVar_hsa_circ_374300,RMVar_hsa_circ_41349,RMVar_hsa_circ_171488,RMVar_hsa_circ_171485,RMVar_hsa_circ_171486,RMVar_hsa_circ_294938,RMVar_hsa_circ_310153,RMVar_hsa_circ_171487,RMVar_hsa_circ_300810,RMVar_hsa_circ_171489 111989 RMVar_ID_111989 Human_SNP_ID_824235204 m1A Human chr15 - 99708852 99708852 99708852 CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACAGGCACACCCTCTCCCAAGAGCACTCTGCCTCC CCGTCCCGCCCGCAAACTCCTAGCCTTTGTACGGGCACACCCTCTCCCAAGAGCACTCTGCCTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:99708828..99708934 26863196 MeRIP-seq:(Medium) rs167805 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_12475,GWAS_ID_12476,GWAS_ID_12477 111990 RMVar_ID_111990 Human_SNP_ID_824253906 m1A Human chr15 - 72686253 72686253 72686253 CGGCCGGGCAACTAAAGAGAATCTCGGCGCTCACCGTCGCGACTCTCTCCTCAGCCATTTTAGCT CGGCCGGGCAACTAAAGAGAATCTCGGCGCTCTCCGTCGCGACTCTCTCCTCAGCCATTTTAGCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:72686242..72686441 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 2 head and neck Human_RBP_ID_5494679,Human_RBP_ID_23127806 111991 RMVar_ID_111991 Human_SNP_ID_824262778 m1A Human chr15 + 73592110 73592110 73592110 TGACAGGGAGAACAGGGCTGTCTCGAATAATGACCTCTTCACTGGTGACAATCCTTGGCTCTGTA TGACAGGGAGAACAGGGCTGTCTCGAATAATGGCCTCTTCACTGGTGACAATCCTTGGCTCTGTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:73592059..73592178 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 4 stomach 111992 RMVar_ID_111992 Human_SNP_ID_824285299 m1A Human chr15 + 39934251 39934251 39934251 CGGGCGCGGCCGGGACGAGCCTCCGGAGAGCTACCCGCAACGACAGGACCACGAGCTACAGGCCC CGGGCGCGGCCGGGACGAGCCTCCGGAGAGCTGCCCGCAACGACAGGACCACGAGCTACAGGCCC A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr15:39934151..39934300 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 8 uterus,large intestine Human_RBP_ID_4342554,Human_RBP_ID_8803778,Human_RBP_ID_9283581,Human_RBP_ID_27810066 Human_Splice_Rec_1583067,Human_Splice_Rec_1583143,Human_Splice_Rec_1583163 RMVar_hsa_circ_105405,RMVar_hsa_circ_170835 111993 RMVar_ID_111993 Human_SNP_ID_824295948 m1A Human chr15 - 64953547 64953547 64953547 GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAAGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG GAACTAAGAAGAAGGAGGAAGAAAGAAGGAGAGGGAAGAAGGAGAGGAGAAGAAGGAAGAAGGAG T C NONHSAG017175.2 RNACentral:URS00009B00E0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:64953498..64953599 26863196 MeRIP-seq:(Medium) rs1482170944 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 111994 RMVar_ID_111994 Human_SNP_ID_824297471 m1A Human chr15 - 72207157 72207157 72207157 GCTCAGAAGATGATGATTGGACGGTGCAACCGAGCTGGGAAGCCTGTCATCTGTGCTACTCAGGC GCTCAGAAGATGATGATTGGACGGTGCAACCGGGCTGGGAAGCCTGTCATCTGTGCTACTCAGGC T C PKM Ensembl:ENSG00000067225 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72207151..72207175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 10 stomach Human_RBP_ID_462846,Human_RBP_ID_758601,Human_RBP_ID_814307,Human_RBP_ID_887145,Human_RBP_ID_1001906,Human_RBP_ID_1507871,Human_RBP_ID_1833445,Human_RBP_ID_3481673,Human_RBP_ID_3946514,Human_RBP_ID_4331857,Human_RBP_ID_5180553,Human_RBP_ID_6458337,Human_RBP_ID_8421910,Human_RBP_ID_8801997,Human_RBP_ID_9283706,Human_RBP_ID_9371129,Human_RBP_ID_12577054,Human_RBP_ID_17250966,Human_RBP_ID_17688965,Human_RBP_ID_17870196,Human_RBP_ID_18469541,Human_RBP_ID_18667415,Human_RBP_ID_18982372,Human_RBP_ID_19067388,Human_RBP_ID_22426214,Human_RBP_ID_22439853,Human_RBP_ID_22799185,Human_RBP_ID_23664668,Human_RBP_ID_26934070,Human_RBP_ID_27155659,Human_RBP_ID_27233703,Human_RBP_ID_27436692 Human_miRNA_ID_2590216,Human_miRNA_ID_2590217,Human_miRNA_ID_2590218 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_36554,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173692,RMVar_hsa_circ_125575,RMVar_hsa_circ_173691,RMVar_hsa_circ_369302,RMVar_hsa_circ_173693,RMVar_hsa_circ_122708,RMVar_hsa_circ_298450,RMVar_hsa_circ_326039,RMVar_hsa_circ_295113,RMVar_hsa_circ_47385,RMVar_hsa_circ_173698,RMVar_hsa_circ_110471,RMVar_hsa_circ_173695,RMVar_hsa_circ_173696,RMVar_hsa_circ_173694,RMVar_hsa_circ_103356,RMVar_hsa_circ_173697 111995 RMVar_ID_111995 Human_SNP_ID_824297476 m1A Human chr15 - 72207157 72207157 72207157 GCTCAGAAGATGATGATTGGACGGTGCAACCGAGCTGGGAAGCCTGTCATCTGTGCTACTCAGGC GCTCAGAAGATGATGATTGGACGGTGCAACCGTGCTGGGAAGCCTGTCATCTGTGCTACTCAGGC T A PKM Ensembl:ENSG00000067225 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:72207151..72207175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 10 lung Human_RBP_ID_462846,Human_RBP_ID_758601,Human_RBP_ID_814307,Human_RBP_ID_887145,Human_RBP_ID_1001906,Human_RBP_ID_1507871,Human_RBP_ID_1833445,Human_RBP_ID_3481673,Human_RBP_ID_3946514,Human_RBP_ID_4331857,Human_RBP_ID_5180553,Human_RBP_ID_6458337,Human_RBP_ID_8421910,Human_RBP_ID_8801997,Human_RBP_ID_9283706,Human_RBP_ID_9371129,Human_RBP_ID_12577054,Human_RBP_ID_17250966,Human_RBP_ID_17688965,Human_RBP_ID_17870196,Human_RBP_ID_18469541,Human_RBP_ID_18667415,Human_RBP_ID_18982372,Human_RBP_ID_19067388,Human_RBP_ID_22426214,Human_RBP_ID_22439853,Human_RBP_ID_22799185,Human_RBP_ID_23664668,Human_RBP_ID_26934070,Human_RBP_ID_27155659,Human_RBP_ID_27233703,Human_RBP_ID_27436692 Human_miRNA_ID_2590216,Human_miRNA_ID_2590217,Human_miRNA_ID_2590218 RMVar_hsa_circ_95588,RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_36554,RMVar_hsa_circ_173681,RMVar_hsa_circ_79654,RMVar_hsa_circ_87889,RMVar_hsa_circ_173685,RMVar_hsa_circ_76441,RMVar_hsa_circ_78497,RMVar_hsa_circ_173686,RMVar_hsa_circ_173683,RMVar_hsa_circ_173684,RMVar_hsa_circ_173682,RMVar_hsa_circ_123928,RMVar_hsa_circ_173679,RMVar_hsa_circ_173680,RMVar_hsa_circ_173678,RMVar_hsa_circ_173692,RMVar_hsa_circ_125575,RMVar_hsa_circ_173691,RMVar_hsa_circ_369302,RMVar_hsa_circ_173693,RMVar_hsa_circ_122708,RMVar_hsa_circ_298450,RMVar_hsa_circ_326039,RMVar_hsa_circ_295113,RMVar_hsa_circ_47385,RMVar_hsa_circ_173698,RMVar_hsa_circ_110471,RMVar_hsa_circ_173695,RMVar_hsa_circ_173696,RMVar_hsa_circ_173694,RMVar_hsa_circ_103356,RMVar_hsa_circ_173697 111996 RMVar_ID_111996 Human_SNP_ID_824305598 m1A Human chr15 + 43795034 43795034 43795034 AGACTGGAGGATATTTGTTATCTGGGGATATGATGCGGTGGCGGCGGCGCCTCAAGATAAGGGGC AGACTGGAGGATATTTGTTATCTGGGGATATGTTGCGGTGGCGGCGGCGCCTCAAGATAAGGGGC A T SERF2 Ensembl:ENSG00000140264 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:43794983..43795050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue 111997 RMVar_ID_111997 Human_SNP_ID_824306776 m1A Human chr15 - 65133746 65133746 65133746 GCCCTGCCACCATTCTTCGGCCAGGGTCGCCCAGGCCCACCGCCCCCGCAGCCGCCGCCTCCTGC GCCCTGCCACCATTCTTCGGCCAGGGTCGCCCGGGCCCACCGCCCCCGCAGCCGCCGCCTCCTGC T C PDCD7 Ensembl:ENSG00000090470 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr15:65133629..65133800;chr15:65133584..65133796 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_232519,Human_RBP_ID_9324298 111998 RMVar_ID_111998 Human_SNP_ID_824316705 m1A Human chr15 + 88630138 88630138 88630138 GAGCTCTACCGGCTGGTGGAGGTGCAGTGGGAACAGCAGGAGGCCCGCAGCCTCTGGACCTGCCC GAGCTCTACCGGCTGGTGGAGGTGCAGTGGGAGCAGCAGGAGGCCCGCAGCCTCTGGACCTGCCC A G AEN Ensembl:ENSG00000181026 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:88629213..88630144 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck Human_RBP_ID_232387,Human_RBP_ID_6476984,Human_RBP_ID_8802881,Human_RBP_ID_12628188,Human_RBP_ID_23127680 Human_Splice_Rec_1640794,Human_Splice_Rec_1640802 Human_miRNA_ID_2512604,Human_miRNA_ID_3055426 RMVar_hsa_circ_90240,RMVar_hsa_circ_124659,RMVar_hsa_circ_121013,RMVar_hsa_circ_174597,RMVar_hsa_circ_174598,RMVar_hsa_circ_174599 111999 RMVar_ID_111999 Human_SNP_ID_824318298 m1A Human chr15 - 56443705 56443705 56443705 AAAAATCATAGAGTTTGCTAACATGCAGCAGCAAAGAGAAGAAGATCGGATGGCAAAAGTTCAAG AAAAATCATAGAGTTTGCTAACATGCAGCAGCCAAGAGAAGAAGATCGGATGGCAAAAGTTCAAG T G MNS1 Ensembl:ENSG00000138587 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:56434295..56456459 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_Splice_Rec_1605869 RMVar_hsa_circ_172314,RMVar_hsa_circ_365475 112000 RMVar_ID_112000 Human_SNP_ID_824343827 m1A Human chr15 + 78162313 78162313 78162313 GAGCAAGCGCATTGCTGAGTTTGCCTTTGAGTATGCCCGGAACAACCACCGGAGCAACGTCACGG GAGCAAGCGCATTGCTGAGTTTGCCTTTGAGTGTGCCCGGAACAACCACCGGAGCAACGTCACGG A G IDH3A Ensembl:ENSG00000166411 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:78162223..78162375 26863196 MeRIP-seq:(Medium) rs1303775777 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_42475,Human_RBP_ID_232269,Human_RBP_ID_8423649,Human_RBP_ID_9056732,Human_RBP_ID_23668697 Human_Splice_Rec_1631400,Human_Splice_Rec_1631401,Human_Splice_Rec_1631418,Human_Splice_Rec_1631419,Human_Splice_Rec_1631440,Human_Splice_Rec_1631441,Human_Splice_Rec_1631466,Human_Splice_Rec_1631476,Human_Splice_Rec_1631477,Human_Splice_Rec_1631530,Human_Splice_Rec_1631538,Human_Splice_Rec_1631539,Human_Splice_Rec_1631551,Human_Splice_Rec_1631568,Human_Splice_Rec_1631569,Human_Splice_Rec_1631604,Human_Splice_Rec_1631605,Human_Splice_Rec_1631616,Human_Splice_Rec_1631617 RMVar_hsa_circ_26221,RMVar_hsa_circ_332699,RMVar_hsa_circ_296820,RMVar_hsa_circ_65626,RMVar_hsa_circ_305295,RMVar_hsa_circ_353367,RMVar_hsa_circ_174151,RMVar_hsa_circ_325525,RMVar_hsa_circ_174154,RMVar_hsa_circ_303886,RMVar_hsa_circ_174153,RMVar_hsa_circ_331170 112001 RMVar_ID_112001 Human_SNP_ID_824357924 m1A Human chr15 - 40776606 40776606 40776606 CTTGTGTCTAGACCTGGAGGCCCGGGAGCGGCAGGCCCAGGCCCAGGAGAGTGAGGAGGAAGAGG CTTGTGTCTAGACCTGGAGGCCCGGGAGCGGCCGGCCCAGGCCCAGGAGAGTGAGGAGGAAGAGG T G DNAJC17 Ensembl:ENSG00000104129 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:40776496..40776664 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_814769,Human_RBP_ID_885409,Human_RBP_ID_18982082,Human_RBP_ID_26327342,Human_RBP_ID_27809339 Human_Splice_Rec_1585308,Human_Splice_Rec_1585309,Human_Splice_Rec_1585338,Human_Splice_Rec_1585339,Human_Splice_Rec_1585360,Human_Splice_Rec_1585361,Human_Splice_Rec_1585392,Human_Splice_Rec_1585393,Human_Splice_Rec_1585408,Human_Splice_Rec_1585409,Human_Splice_Rec_1585424,Human_Splice_Rec_1585425,Human_Splice_Rec_1585429,Human_Splice_Rec_1585440,Human_Splice_Rec_1585441 RMVar_hsa_circ_170953,RMVar_hsa_circ_102200,RMVar_hsa_circ_108598,RMVar_hsa_circ_170954,RMVar_hsa_circ_279175,RMVar_hsa_circ_322385,RMVar_hsa_circ_324364,RMVar_hsa_circ_125059,RMVar_hsa_circ_170957,RMVar_hsa_circ_170958,RMVar_hsa_circ_170959,RMVar_hsa_circ_170956 112002 RMVar_ID_112002 Human_SNP_ID_824364369 m1A Human chr15 - 76340233 76340233 76340233 AGGGTGAGGCCAGAGGTTAGCGAGGGGCCGCCACCCACCCGCCCCGAGCCCAACCTCCGGGTGGC AGGGTGAGGCCAGAGGTTAGCGAGGGGCCGCCCCCCACCCGCCCCGAGCCCAACCTCCGGGTGGC T G AC027243.2 Ensembl:ENSG00000259514 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:76340139..76340253 26863196 MeRIP-seq:(Medium) rs757231186 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5287860 112003 RMVar_ID_112003 Human_SNP_ID_824379634 m1A Human chr15 + 92162902 92162902 92162902 GATACCTGTATGTCAGCATCGCCATCGCGCTCAAATCCTTCGCCTTCATCCTGTACACCACCACG GATACCTGTATGTCAGCATCGCCATCGCGCTCGAATCCTTCGCCTTCATCCTGTACACCACCACG A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:92162776..92172045 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_27438341 Human_Splice_Rec_1646565 Human_miRNA_ID_2875792 RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 112004 RMVar_ID_112004 Human_SNP_ID_824393743 m1A Human chr15 + 72474923 72474923 72474923 CGGCGGTGGTGGTGGCGGGCCGGGGCATGAGCAGGAGGAGGATTACCGCTACGAGGTGCTCACGG CGGCGGTGGTGGTGGCGGGCCGGGGCATGAGCGGGAGGAGGATTACCGCTACGAGGTGCTCACGG A G ARIH1 Ensembl:ENSG00000166233 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr15:72474821..72475025;chr15:72474870..72474970 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3945695,Human_RBP_ID_9324344,Human_RBP_ID_18411250,Human_RBP_ID_18436777,Human_RBP_ID_22047562,Human_RBP_ID_26778691 Human_Splice_Rec_1622933,Human_Splice_Rec_1622959,Human_Splice_Rec_1622967,Human_Splice_Rec_1622973 RMVar_hsa_circ_173735 112005 RMVar_ID_112005 Human_SNP_ID_824400899 m1A Human chr15 + 30904475 30904475 30904475 TCAGAGTTCGCTTTTCCCCTTGCTGAATTCATAAAAATGTTTTTAATTTATATGTGTTTCTTCTT TCAGAGTTCGCTTTTCCCCTTGCTGAATTCATTAAAATGTTTTTAATTTATATGTGTTTCTTCTT A T FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:30904472..30904598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1277893 112006 RMVar_ID_112006 Human_SNP_ID_824442403 m1A Human chr15 + 100893992 100893992 100893992 TTCCCCCTGCTGATGCTGGTGTGGAAGCTGGCACCCGCCCTCTGCTGTGGGAACACCATGGTCCT TTCCCCCTGCTGATGCTGGTGTGGAAGCTGGCGCCCGCCCTCTGCTGTGGGAACACCATGGTCCT A G ALDH1A3 Ensembl:ENSG00000184254 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:100892593..100893995 32194978 MeRIP-seq:(Medium) rs1436859231 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_Splice_Rec_1650846,Human_Splice_Rec_1650847,Human_Splice_Rec_1650858,Human_Splice_Rec_1650859 112007 RMVar_ID_112007 Human_SNP_ID_824443156 m1A Human chr15 - 74937975 74937975 74937975 GCGCCGCTCTCCGCCGCTGCGCTGTGGCCGCAACCACCCGGGCCGACCCTCGAGGCCTCCTGCAC GCGCCGCTCTCCGCCGCTGCGCTGTGGCCGCACCCACCCGGGCCGACCCTCGAGGCCTCCTGCAC T G COX5A Ensembl:ENSG00000178741 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 50c;HTR8/Svneo,Normoxia chr15:74929151..74938100;chr15:74937924..74938071 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_232366,Human_RBP_ID_463768,Human_RBP_ID_759268,Human_RBP_ID_815166,Human_RBP_ID_887597,Human_RBP_ID_4333849,Human_RBP_ID_9056410,Human_RBP_ID_9324355,Human_RBP_ID_22532611,Human_RBP_ID_26435975,Human_RBP_ID_26809107 Human_Splice_Rec_1627411,Human_Splice_Rec_1627419,Human_Splice_Rec_1627423,Human_Splice_Rec_1627429,Human_Splice_Rec_1627443 RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 112008 RMVar_ID_112008 Human_SNP_ID_824444344 m1A Human chr15 + 43824568 43824568 43824568 GCGGTTGCTTCATGAGAGCGCTTGGGACCGACATGTTGATGGCAGCGACGGTGATTCCCGAAACT GCGGTTGCTTCATGAGAGCGCTTGGGACCGACTTGTTGATGGCAGCGACGGTGATTCCCGAAACT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43824490..43824656 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck 112009 RMVar_ID_112009 Human_SNP_ID_824469817 m1A Human chr15 - 34904487 34904487 34904487 TTCAAATTGTCCAGGACCTGAACCCAGACCCAATCTTAGAGGAGAATCAAGGACATTTAGAGTGT TTCAAATTGTCCAGGACCTGAACCCAGACCCATTCTTAGAGGAGAATCAAGGACATTTAGAGTGT T A AQR Ensembl:ENSG00000021776 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:34904384..34906598 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_888110,Human_RBP_ID_12490790 Human_Splice_Rec_1581188,Human_Splice_Rec_1581256 RMVar_hsa_circ_108498,RMVar_hsa_circ_78233,RMVar_hsa_circ_170555,RMVar_hsa_circ_78892,RMVar_hsa_circ_170558,RMVar_hsa_circ_114293,RMVar_hsa_circ_170561,RMVar_hsa_circ_84856,RMVar_hsa_circ_170562,RMVar_hsa_circ_170559,RMVar_hsa_circ_170560,RMVar_hsa_circ_37484,RMVar_hsa_circ_14096,RMVar_hsa_circ_22603,RMVar_hsa_circ_2164,RMVar_hsa_circ_2677,RMVar_hsa_circ_4028,RMVar_hsa_circ_39524,RMVar_hsa_circ_72643,RMVar_hsa_circ_117097,RMVar_hsa_circ_35893,RMVar_hsa_circ_80628,RMVar_hsa_circ_170567,RMVar_hsa_circ_121343,RMVar_hsa_circ_170568,RMVar_hsa_circ_368757,RMVar_hsa_circ_307777,RMVar_hsa_circ_89078,RMVar_hsa_circ_79367,RMVar_hsa_circ_23784,RMVar_hsa_circ_8730,RMVar_hsa_circ_170571,RMVar_hsa_circ_170572,RMVar_hsa_circ_170569,RMVar_hsa_circ_170570,RMVar_hsa_circ_170577,RMVar_hsa_circ_36603,RMVar_hsa_circ_170578,RMVar_hsa_circ_113132,RMVar_hsa_circ_315239,RMVar_hsa_circ_170579,RMVar_hsa_circ_328360,RMVar_hsa_circ_30848,RMVar_hsa_circ_21505,RMVar_hsa_circ_31574,RMVar_hsa_circ_170581,RMVar_hsa_circ_8649,RMVar_hsa_circ_9712,RMVar_hsa_circ_368235,RMVar_hsa_circ_170580,RMVar_hsa_circ_268147,RMVar_hsa_circ_60365,RMVar_hsa_circ_267427,RMVar_hsa_circ_377691,RMVar_hsa_circ_115011,RMVar_hsa_circ_293486,RMVar_hsa_circ_170586,RMVar_hsa_circ_372596,RMVar_hsa_circ_373182,RMVar_hsa_circ_371808,RMVar_hsa_circ_318789,RMVar_hsa_circ_117779,RMVar_hsa_circ_121392,RMVar_hsa_circ_84278,RMVar_hsa_circ_170587,RMVar_hsa_circ_170591,RMVar_hsa_circ_170593,RMVar_hsa_circ_26436,RMVar_hsa_circ_170594,RMVar_hsa_circ_170592,RMVar_hsa_circ_170589,RMVar_hsa_circ_170590,RMVar_hsa_circ_170588,RMVar_hsa_circ_32035,RMVar_hsa_circ_106178,RMVar_hsa_circ_170595 112010 RMVar_ID_112010 Human_SNP_ID_824484116 m1A Human chr15 - 64688519 64688519 64688519 GTTGAAATTGTTTTCCATAAAGAACAGTATAAACATATTATTCACATGTAATCACCAATAGTAAA GTTGAAATTGTTTTCCATAAAGAACAGTATAAGCATATTATTCACATGTAATCACCAATAGTAAA T C OAZ2 Ensembl:ENSG00000180304 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64688468..64688719 32194978 MeRIP-seq:(Medium) rs942660779 Functional Loss SNV COSMIC 33..33 33 meninges atypical 3 brain Human_RBP_ID_1001391,Human_RBP_ID_1506365,Human_RBP_ID_1831758,Human_RBP_ID_6448126,Human_RBP_ID_8080752,Human_RBP_ID_17250576,Human_RBP_ID_17483110,Human_RBP_ID_17864025,Human_RBP_ID_26633156,Human_RBP_ID_27436019,Human_RBP_ID_27653162 RMVar_hsa_circ_173059,RMVar_hsa_circ_80160,RMVar_hsa_circ_121624,RMVar_hsa_circ_173060 112011 RMVar_ID_112011 Human_SNP_ID_824494887 m1A Human chr15 - 64749495 64749495 64749495 GAGATATAAGGGTGTTCTCTCTTTTTCCTACTAGCCTGTTGGTTTTGTGATCTTTGACAGCCGTG GAGATATAAGGGTGTTCTCTCTTTTTCCTACTTGCCTGTTGGTTTTGTGATCTTTGACAGCCGTG T A RBPMS2 Ensembl:ENSG00000166831 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:64749465..64751592 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_Splice_Rec_1613473,Human_Splice_Rec_1613487 RMVar_hsa_circ_293303,RMVar_hsa_circ_346091,RMVar_hsa_circ_376611 112012 RMVar_ID_112012 Human_SNP_ID_824498828 m1A Human chr15 + 66387043 66387041 66387043 GTGCCGCCCGAGCCGGAGGGACTGGTTGGTTGAGAGAGAGAGAGGAAGGGAATCCCGGGCTGCCG GTGCCGCCCGAGCCGGAGGGACTGGTTGGTT__GAGAGAGAGAGGAAGGGAATCCCGGGCTGCCG TGA T MAP2K1 Ensembl:ENSG00000169032 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66386926..66387125 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 ESCA 1 - Human_RBP_ID_461733,Human_RBP_ID_4329404,Human_RBP_ID_5141276,Human_RBP_ID_5316092,Human_RBP_ID_5495046,Human_RBP_ID_8804093,Human_RBP_ID_8941196,Human_RBP_ID_9324300,Human_RBP_ID_9418462,Human_RBP_ID_18418488,Human_RBP_ID_22440047,Human_RBP_ID_23661664 RMVar_hsa_circ_126868,RMVar_hsa_circ_173294 112013 RMVar_ID_112013 Human_SNP_ID_824501196 m1A Human chr15 - 101277406 101277406 101277406 GCGGCGGCGGCGGCGGCGGTCATGGAACGCCAAGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA GCGGCGGCGGCGGCGGCGGTCATGGAACGCCATGAGGAGTCTCTGTCCGCGCGGCCGGCCCTGGA T A SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:101277323..101277454 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_759941,Human_RBP_ID_1129685,Human_RBP_ID_1503288,Human_RBP_ID_4315916,Human_RBP_ID_5464618,Human_RBP_ID_9371963 Human_Splice_Rec_1651193,Human_Splice_Rec_1651223,Human_Splice_Rec_1651243,Human_Splice_Rec_1651249,Human_Splice_Rec_1651253 112014 RMVar_ID_112014 Human_SNP_ID_824538846 m1A Human chr15 + 74620059 74620051 74620059 CCAGAGGAGGTACCGGGAGCGCCGTGACAGCGATACATACCGGTGTGAAGAGCGGAGCCCATCCT CCAGAGGAGGTACCGGGAGCGCCGT________TACATACCGGTGTGAAGAGCGGAGCCCATCCT TGACAGCGA T CLK3 Ensembl:ENSG00000179335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:74619974..74620174 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 26..33 33 ESCA 1 - Human_RBP_ID_885773,Human_RBP_ID_9371138,Human_RBP_ID_17870212,Human_RBP_ID_18982407,Human_RBP_ID_26327720 Human_Splice_Rec_1625752,Human_Splice_Rec_1625776,Human_Splice_Rec_1625798,Human_Splice_Rec_1625802,Human_Splice_Rec_1625826,Human_Splice_Rec_1625848,Human_Splice_Rec_1625860,Human_Splice_Rec_1625870,Human_Splice_Rec_1625880,Human_Splice_Rec_1625886,Human_Splice_Rec_1625896,Human_Splice_Rec_1625908,Human_Splice_Rec_1625910,Human_Splice_Rec_1625914 Human_miRNA_ID_2576612 RMVar_hsa_circ_320709,RMVar_hsa_circ_361241,RMVar_hsa_circ_370113,RMVar_hsa_circ_346961,RMVar_hsa_circ_281818,RMVar_hsa_circ_50702,RMVar_hsa_circ_173873,RMVar_hsa_circ_173874,RMVar_hsa_circ_79814,RMVar_hsa_circ_173875 112015 RMVar_ID_112015 Human_SNP_ID_824542832 m1A Human chr15 + 84797952 84797952 84797952 CATCCAGGAGCGACACTGCCAGGTTTTCCACAAATGTGCATTCTGCCCCATGGCCTTCAAGACTG CATCCAGGAGCGACACTGCCAGGTTTTCCACAGATGTGCATTCTGCCCCATGGCCTTCAAGACTG A G ZNF592 Ensembl:ENSG00000166716 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:84797851..84798050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_6475192 Human_Splice_Rec_1638616,Human_Splice_Rec_1638617,Human_Splice_Rec_1638632,Human_Splice_Rec_1638633,Human_Splice_Rec_1638646,Human_Splice_Rec_1638647 RMVar_hsa_circ_120468,RMVar_hsa_circ_174467,RMVar_hsa_circ_124655,RMVar_hsa_circ_174466,RMVar_hsa_circ_376202,RMVar_hsa_circ_174468,RMVar_hsa_circ_320721 112016 RMVar_ID_112016 Human_SNP_ID_824570509 m1A Human chr15 + 67164997 67164997 67164997 CGATGGCCAGACCTGCACAGCCACCACGAGCTACGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA CGATGGCCAGACCTGCACAGCCACCACGAGCTGCGGGCCATGGAGCTGTGTGAGTTCGCCTTCAA A G SMAD3 Ensembl:ENSG00000166949 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1065080 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_18981608,Human_RBP_ID_26809038,Human_RBP_ID_27810465 Human_Splice_Rec_1616591,Human_Splice_Rec_1616597,Human_Splice_Rec_1616613,Human_Splice_Rec_1616621,Human_Splice_Rec_1616629,Human_Splice_Rec_1616645,Human_Splice_Rec_1616657,Human_Splice_Rec_1616673 Human_miRNA_ID_2450745,Human_miRNA_ID_2450746,Human_miRNA_ID_2540206,Human_miRNA_ID_2540207 Clinvar_Rec_569 GWAS_ID_12729,GWAS_ID_12730,GWAS_ID_12731,GWAS_ID_12732,GWAS_ID_12733,GWAS_ID_12734,GWAS_ID_12735 RMVar_hsa_circ_173349,RMVar_hsa_circ_27493,RMVar_hsa_circ_173348,RMVar_hsa_circ_121746,RMVar_hsa_circ_270136,RMVar_hsa_circ_276738,RMVar_hsa_circ_43918,RMVar_hsa_circ_173350 112017 RMVar_ID_112017 Human_SNP_ID_824578992 m1A Human chr15 + 58883781 58883781 58883781 CCATGGCGTTCAACCACATGTCGCTCCTCAGGATAGTGCTAAAAGAATAGCATATGAAAAGTCAC CCATGGCGTTCAACCACATGTCGCTCCTCAGGGTAGTGCTAAAAGAATAGCATATGAAAAGTCAC A G RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:58883626..58883824 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112018 RMVar_ID_112018 Human_SNP_ID_824595004 m1A Human chr15 - 40767998 40767998 40767998 CCTCGTCATGATGCGCATGCGCCAGGCGGCCGAGCGGCAACAGCTGATCGCACGGATGCAGCAGG CCTCGTCATGATGCGCATGCGCCAGGCGGCCGTGCGGCAACAGCTGATCGCACGGATGCAGCAGG T A DNAJC17 Ensembl:ENSG00000104129 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:40767954..40768028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_1585320,Human_Splice_Rec_1585328,Human_Splice_Rec_1585350,Human_Splice_Rec_1585352 RMVar_hsa_circ_170953,RMVar_hsa_circ_102200,RMVar_hsa_circ_108598,RMVar_hsa_circ_170955,RMVar_hsa_circ_76681,RMVar_hsa_circ_170954 112019 RMVar_ID_112019 Human_SNP_ID_824622463 m1A Human chr15 - 66499620 66499620 66499620 CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACAAGCCAAATCAGATGAGAA CACAAGCTCCGGGTGGATAAGGCAGCTGCTGCCGCAGCGGCACTACAAGCCAAATCAGATGAGAA T G RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:66499376..66499675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_42787,Human_RBP_ID_232351,Human_RBP_ID_461801,Human_RBP_ID_759245,Human_RBP_ID_886567,Human_RBP_ID_1506795,Human_RBP_ID_4346396,Human_RBP_ID_5178946,Human_RBP_ID_6451390,Human_RBP_ID_9371730,Human_RBP_ID_17252004,Human_RBP_ID_17366920,Human_RBP_ID_17484538,Human_RBP_ID_17864627,Human_RBP_ID_22192565,Human_RBP_ID_22496568,Human_RBP_ID_22930240,Human_RBP_ID_25186847,Human_RBP_ID_26435386,Human_RBP_ID_26933045,Human_RBP_ID_27233033 Human_Splice_Rec_1616072,Human_Splice_Rec_1616086,Human_Splice_Rec_1616088,Human_Splice_Rec_1616108,Human_Splice_Rec_1616124,Human_Splice_Rec_1616134 Human_miRNA_ID_2515870 RMVar_hsa_circ_82571,RMVar_hsa_circ_124192,RMVar_hsa_circ_104067,RMVar_hsa_circ_110354,RMVar_hsa_circ_88176,RMVar_hsa_circ_173307,RMVar_hsa_circ_173309,RMVar_hsa_circ_173310,RMVar_hsa_circ_173311,RMVar_hsa_circ_173308 112020 RMVar_ID_112020 Human_SNP_ID_824628185 m1A Human chr15 + 44459055 44459055 44459055 GAGAACACGGAAAGCTTCTCAGCAGTCAAATCAAATCCAAACACAACGCACTGCCAGAGCAAAGA GAGAACACGGAAAGCTTCTCAGCAGTCAAATCTAATCCAAACACAACGCACTGCCAGAGCAAAGA A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:44458952..44459061 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 salivary_gland salivary_duct_carcinoma 3 head and neck Human_RBP_ID_1000742,Human_RBP_ID_9282994,Human_RBP_ID_17249981,Human_RBP_ID_17365248,Human_RBP_ID_17482187,Human_RBP_ID_17860811,Human_RBP_ID_26326648,Human_RBP_ID_27809455 Human_Splice_Rec_1595368,Human_Splice_Rec_1595376,Human_Splice_Rec_1595400,Human_Splice_Rec_1595406,Human_Splice_Rec_1595430,Human_Splice_Rec_1595436 RMVar_hsa_circ_69757,RMVar_hsa_circ_171584,RMVar_hsa_circ_92000,RMVar_hsa_circ_303487,RMVar_hsa_circ_354023,RMVar_hsa_circ_327814,RMVar_hsa_circ_278698,RMVar_hsa_circ_171587,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_12303,RMVar_hsa_circ_171588,RMVar_hsa_circ_171586 112021 RMVar_ID_112021 Human_SNP_ID_824640186 m1A Human chr15 + 29105476 29105476 29105476 CAATGGCATCAACCCCGAAGACTTGAGCCAGAAGGAATACAGCGACATCATCAACACCCAGGAGA CAATGGCATCAACCCCGAAGACTTGAGCCAGATGGAATACAGCGACATCATCAACACCCAGGAGA A T APBA2 Ensembl:ENSG00000034053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr15:29105426..29105526;chr15:29105426..29108472 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_27810032 Human_Splice_Rec_1574880,Human_Splice_Rec_1574881,Human_Splice_Rec_1574910,Human_Splice_Rec_1574911,Human_Splice_Rec_1574938,Human_Splice_Rec_1574939,Human_Splice_Rec_1574964,Human_Splice_Rec_1574965,Human_Splice_Rec_1575002,Human_Splice_Rec_1575003,Human_Splice_Rec_1575026,Human_Splice_Rec_1575027 112022 RMVar_ID_112022 Human_SNP_ID_824664550 m1A Human chr15 - 34228553 34228553 34228553 GGGGGCTCAATGAAGGCTAACCAATCCGATGCATGTGTAGGTAACAGTCCCATGGACTGGCACTT GGGGGCTCAATGAAGGCTAACCAATCCGATGCTTGTGTAGGTAACAGTCCCATGGACTGGCACTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:34228502..34228613 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112023 RMVar_ID_112023 Human_SNP_ID_824682801 m1A Human chr15 + 74803070 74803070 74803070 CTTGACCATGTTGCACTGTTTGCATGCGCCCGAGGCAGACGTCTGTCAGGGGCTTGGATTTCGTG CTTGACCATGTTGCACTGTTTGCATGCGCCCGGGGCAGACGTCTGTCAGGGGCTTGGATTTCGTG A G CSK Ensembl:ENSG00000103653 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:74802998..74803099 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_463541,Human_RBP_ID_758663,Human_RBP_ID_1175827,Human_RBP_ID_1508384,Human_RBP_ID_5112940,Human_RBP_ID_5141675,Human_RBP_ID_6463393,Human_RBP_ID_8183162,Human_RBP_ID_12590995,Human_RBP_ID_17866521,Human_RBP_ID_21970285,Human_RBP_ID_23666568 Human_miRNA_ID_2455659 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891,RMVar_hsa_circ_124453,RMVar_hsa_circ_173893,RMVar_hsa_circ_94074,RMVar_hsa_circ_103756,RMVar_hsa_circ_173895,RMVar_hsa_circ_173897 112024 RMVar_ID_112024 Human_SNP_ID_824689683 m1A Human chr15 - 66493073 66493073 66493073 GTTATTTTGAGCTGCTTTTAGAGGAAACAGCCAGAAGTTTAAATGAGCATGTTCCTTAGAACACA GTTATTTTGAGCTGCTTTTAGAGGAAACAGCCGGAAGTTTAAATGAGCATGTTCCTTAGAACACA T C SNAPC5 Ensembl:ENSG00000174446 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12594835 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1001562 GWAS_ID_12723,GWAS_ID_12724,GWAS_ID_12725,GWAS_ID_12726,GWAS_ID_12727,GWAS_ID_12728 112025 RMVar_ID_112025 Human_SNP_ID_824702412 m1A Human chr15 - 41972428 41972428 41972428 GCGAACGCGCTGGCGGCGCGGACGCGGTGCAGACGGTGACGGGCGGGCTGCGCTCGCTCTACCTG GCGAACGCGCTGGCGGCGCGGACGCGGTGCAGGCGGTGACGGGCGGGCTGCGCTCGCTCTACCTG T C EHD4 Ensembl:ENSG00000103966 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:41972378..41972528 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 1 skin,head and neck 112026 RMVar_ID_112026 Human_SNP_ID_824725048 m1A Human chr15 - 33999549 33999549 33999549 GATGACACTAGGTTTTGGGTCTGAACAGTGAGAAGAAGGGAGTTGCCCTTAACTGAGGTGTGTAA GATGACACTAGGTTTTGGGTCTGAACAGTGAGTAGAAGGGAGTTGCCCTTAACTGAGGTGTGTAA T A AVEN Ensembl:ENSG00000169857 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:33999543..33999634 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_170517,RMVar_hsa_circ_100574,RMVar_hsa_circ_170516,RMVar_hsa_circ_84374 112027 RMVar_ID_112027 Human_SNP_ID_824765321 m1A Human chr15 - 70891882 70891882 70891882 ATTCTGAGGCTGCCCCAGGTCCAGTCTCCTGTACACGCCCCCGAGCTGGGAAGCAGGCTGCAGCT ATTCTGAGGCTGCCCCAGGTCCAGTCTCCTGTGCACGCCCCCGAGCTGGGAAGCAGGCTGCAGCT T C THAP10 Ensembl:ENSG00000129028 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:70882900..70891986 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_1620887 112028 RMVar_ID_112028 Human_SNP_ID_824772698 m1A Human chr15 - 66435104 66435104 66435104 TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGAAAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGATAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66435053..66435135 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic,face desmoplastic 1 skin,head and neck 112029 RMVar_ID_112029 Human_SNP_ID_824772711 m1A Human chr15 - 66435104 66435104 66435104 TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGAAAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA TCAGTTCTCCCACCTTCTGCTTCTGGGTAAGACAGGCCTCAAGGCGCTTTCGCTGCTGCTCATCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66435053..66435135 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 lung,haematopoietic and lymphoid tissue 112030 RMVar_ID_112030 Human_SNP_ID_824775793 m1A Human chr15 + 44288834 44288834 44288834 GGTTCAAAGCCTCCGGAACGCGTTTTGGCCTGATTTGAGGAGGGGGGCGGGGAGGGACCTGCGGC GGTTCAAAGCCTCCGGAACGCGTTTTGGCCTGCTTTGAGGAGGGGGGCGGGGAGGGACCTGCGGC A C CASC4 Ensembl:ENSG00000166734 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:44288783..44288879 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4322995,Human_RBP_ID_18663180,Human_RBP_ID_22439773 Human_Splice_Rec_1595275,Human_Splice_Rec_1595295 112031 RMVar_ID_112031 Human_SNP_ID_824790140 m1A Human chr15 + 78162282 78162282 78162282 TGCAGAGTATCAAGCTCATCACCGAGGGGGCGAGCAAGCGCATTGCTGAGTTTGCCTTTGAGTAT TGCAGAGTATCAAGCTCATCACCGAGGGGGCGCGCAAGCGCATTGCTGAGTTTGCCTTTGAGTAT A C IDH3A Ensembl:ENSG00000166411 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:78162226..78162381 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 3 liver Human_RBP_ID_464645,Human_RBP_ID_1002246 Human_Splice_Rec_1631400,Human_Splice_Rec_1631401,Human_Splice_Rec_1631418,Human_Splice_Rec_1631419,Human_Splice_Rec_1631440,Human_Splice_Rec_1631441,Human_Splice_Rec_1631466,Human_Splice_Rec_1631476,Human_Splice_Rec_1631477,Human_Splice_Rec_1631530,Human_Splice_Rec_1631538,Human_Splice_Rec_1631539,Human_Splice_Rec_1631550,Human_Splice_Rec_1631551,Human_Splice_Rec_1631568,Human_Splice_Rec_1631569,Human_Splice_Rec_1631604,Human_Splice_Rec_1631605,Human_Splice_Rec_1631616,Human_Splice_Rec_1631617 RMVar_hsa_circ_26221,RMVar_hsa_circ_332699,RMVar_hsa_circ_296820,RMVar_hsa_circ_65626,RMVar_hsa_circ_305295,RMVar_hsa_circ_353367,RMVar_hsa_circ_174151,RMVar_hsa_circ_325525,RMVar_hsa_circ_174154,RMVar_hsa_circ_303886,RMVar_hsa_circ_174153,RMVar_hsa_circ_331170 112032 RMVar_ID_112032 Human_SNP_ID_824796356 m1A Human chr15 - 72230999 72230999 72230999 CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCAGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA CCCGGGCACGCAGGCAGGGCGGCGCAGGATCCGGGGCGTCTGGGATGCAGTGGAGCTCAGAGAGA T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:72230997..72231225 26863196 MeRIP-seq:(Medium) rs890312 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_12577639 GWAS_ID_12737,GWAS_ID_12738,GWAS_ID_12739,GWAS_ID_12740,GWAS_ID_12741,GWAS_ID_12742,GWAS_ID_12743,GWAS_ID_12744,GWAS_ID_12745,GWAS_ID_12746,GWAS_ID_12747,GWAS_ID_12748,GWAS_ID_12749,GWAS_ID_12750,GWAS_ID_12751,GWAS_ID_12752,GWAS_ID_12753,GWAS_ID_12754,GWAS_ID_12755,GWAS_ID_12756,GWAS_ID_12757 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_127337,RMVar_hsa_circ_173704 112033 RMVar_ID_112033 Human_SNP_ID_824801365 m1A Human chr15 - 73983447 73983447 73983447 TGGCGAAGTTACCTGGGGATCCTGGCTGGCCCACCTTCCTGGCTGCAGTCCAGGCCCGTGCTGGC TGGCGAAGTTACCTGGGGATCCTGGCTGGCCCGCCTTCCTGGCTGCAGTCCAGGCCCGTGCTGGC T C STOML1 Ensembl:ENSG00000067221 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2289411 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_26437717 112034 RMVar_ID_112034 Human_SNP_ID_824813041 m1A Human chr15 - 52179705 52179705 52179705 AGCCGGACCGGCTCGCCACTTCCCGGGCGGGGACGGCGGGGGCGGTGGGGGCGGTCGTGGCTGCG AGCCGGACCGGCTCGCCACTTCCCGGGCGGGGGCGGCGGGGGCGGTGGGGGCGGTCGTGGCTGCG T C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:52179698..52179946 26863196 MeRIP-seq:(Medium) rs1033291614 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5354961 RMVar_hsa_circ_114898,RMVar_hsa_circ_172134 112035 RMVar_ID_112035 Human_SNP_ID_824823010 m1A Human chr15 + 92924460 92924460 92924460 CTGAATCTTCTGAGAGTCAGTCGGAATCTGAGAGCGAATCAGCAGGTTCCAAATCCCAGCCAGTC CTGAATCTTCTGAGAGTCAGTCGGAATCTGAGCGCGAATCAGCAGGTTCCAAATCCCAGCCAGTC A C CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:92924329..92939646 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_5023,Human_RBP_ID_42669,Human_RBP_ID_1511250,Human_RBP_ID_9371295,Human_RBP_ID_12642778,Human_RBP_ID_18672106,Human_RBP_ID_24544153,Human_RBP_ID_26327888,Human_RBP_ID_27809920 Human_Splice_Rec_1646845,Human_Splice_Rec_1646853,Human_Splice_Rec_1646873,Human_Splice_Rec_1646953,Human_Splice_Rec_1646973,Human_Splice_Rec_1646997,Human_Splice_Rec_1647053,Human_Splice_Rec_1647127,Human_Splice_Rec_1647161,Human_Splice_Rec_1647183,Human_Splice_Rec_1647191 RMVar_hsa_circ_50134,RMVar_hsa_circ_62518,RMVar_hsa_circ_28480,RMVar_hsa_circ_74200,RMVar_hsa_circ_98654,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982,RMVar_hsa_circ_174984,RMVar_hsa_circ_79895,RMVar_hsa_circ_174985,RMVar_hsa_circ_268815,RMVar_hsa_circ_360648,RMVar_hsa_circ_363239,RMVar_hsa_circ_359197,RMVar_hsa_circ_126848,RMVar_hsa_circ_61545,RMVar_hsa_circ_66951,RMVar_hsa_circ_32807,RMVar_hsa_circ_75240,RMVar_hsa_circ_292262,RMVar_hsa_circ_323411,RMVar_hsa_circ_357151,RMVar_hsa_circ_362938,RMVar_hsa_circ_174986,RMVar_hsa_circ_371539,RMVar_hsa_circ_359930,RMVar_hsa_circ_341090,RMVar_hsa_circ_345255,RMVar_hsa_circ_328168,RMVar_hsa_circ_320578,RMVar_hsa_circ_321640,RMVar_hsa_circ_312312,RMVar_hsa_circ_269937,RMVar_hsa_circ_272089,RMVar_hsa_circ_88004,RMVar_hsa_circ_63727,RMVar_hsa_circ_64882,RMVar_hsa_circ_69369,RMVar_hsa_circ_64646,RMVar_hsa_circ_61324,RMVar_hsa_circ_63270,RMVar_hsa_circ_57571,RMVar_hsa_circ_174988,RMVar_hsa_circ_174992,RMVar_hsa_circ_174994,RMVar_hsa_circ_174996,RMVar_hsa_circ_174997,RMVar_hsa_circ_174995,RMVar_hsa_circ_174993,RMVar_hsa_circ_174990,RMVar_hsa_circ_174991,RMVar_hsa_circ_174989,RMVar_hsa_circ_174987 112036 RMVar_ID_112036 Human_SNP_ID_824826281 m1A Human chr15 - 74906702 74906702 74906702 GCTCGGGACCGCGCGCCGGGAGCTGCGGGGCCACCCTCCGGGCAGATCGGTAATAGAGCCCTCCG GCTCGGGACCGCGCGCCGGGAGCTGCGGGGCCCCCCTCCGGGCAGATCGGTAATAGAGCCCTCCG T G FAM219B Ensembl:ENSG00000178761 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:74906657..74906790 26863196 MeRIP-seq:(Medium) rs145289460 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_463733,Human_RBP_ID_4342824,Human_RBP_ID_18418395 112037 RMVar_ID_112037 Human_SNP_ID_824839876 m1A Human chr15 + 74787990 74787990 74787990 GCGGGTAGAGGAGACGAGGAGTCAGTGAGGGGAGGCCTGTGGTTCTCACTTCCTGGCAGAGCTGG GCGGGTAGAGGAGACGAGGAGTCAGTGAGGGGGGGCCTGTGGTTCTCACTTCCTGGCAGAGCTGG A G CSK Ensembl:ENSG00000103653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74787986..74788081 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_6463321 RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 112038 RMVar_ID_112038 Human_SNP_ID_824863185 m1A Human chr15 + 93002274 93002274 93002274 GGAGAAACAAATGAGTTCTAGGAAAGACAAAGAAGGGGACAAGGAAAGAAAGAAGTCAAAAGATA GGAGAAACAAATGAGTTCTAGGAAAGACAAAGCAGGGGACAAGGAAAGAAAGAAGTCAAAAGATA A C CHD2 Ensembl:ENSG00000173575 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:93002152..93002368 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_887249,Human_RBP_ID_2462184,Human_RBP_ID_3945935,Human_RBP_ID_5523558,Human_RBP_ID_9345324,Human_RBP_ID_24544186,Human_RBP_ID_26327145,Human_RBP_ID_27809960 Human_Splice_Rec_1646932,Human_Splice_Rec_1646933,Human_Splice_Rec_1647112,Human_Splice_Rec_1647113,Human_Splice_Rec_1647368,Human_Splice_Rec_1647394,Human_Splice_Rec_1647395,Human_Splice_Rec_1647414,Human_Splice_Rec_1647415 RMVar_hsa_circ_22375,RMVar_hsa_circ_98654,RMVar_hsa_circ_174984,RMVar_hsa_circ_362938,RMVar_hsa_circ_88004,RMVar_hsa_circ_63270,RMVar_hsa_circ_174987,RMVar_hsa_circ_60206,RMVar_hsa_circ_88492,RMVar_hsa_circ_175022,RMVar_hsa_circ_53788,RMVar_hsa_circ_175023,RMVar_hsa_circ_70647,RMVar_hsa_circ_19468,RMVar_hsa_circ_72524,RMVar_hsa_circ_56036,RMVar_hsa_circ_16759,RMVar_hsa_circ_365470,RMVar_hsa_circ_175038,RMVar_hsa_circ_94734,RMVar_hsa_circ_55449,RMVar_hsa_circ_74275,RMVar_hsa_circ_119721,RMVar_hsa_circ_175041,RMVar_hsa_circ_356133,RMVar_hsa_circ_103601,RMVar_hsa_circ_175048,RMVar_hsa_circ_175043,RMVar_hsa_circ_265214,RMVar_hsa_circ_283661,RMVar_hsa_circ_369031,RMVar_hsa_circ_302819,RMVar_hsa_circ_175045,RMVar_hsa_circ_175046,RMVar_hsa_circ_122989,RMVar_hsa_circ_277927,RMVar_hsa_circ_353321,RMVar_hsa_circ_364817,RMVar_hsa_circ_334097,RMVar_hsa_circ_271889,RMVar_hsa_circ_175050,RMVar_hsa_circ_175051,RMVar_hsa_circ_175049,RMVar_hsa_circ_72838,RMVar_hsa_circ_336105,RMVar_hsa_circ_352757,RMVar_hsa_circ_363894,RMVar_hsa_circ_296564 112039 RMVar_ID_112039 Human_SNP_ID_824865707 m1A Human chr15 - 75339081 75339081 75339081 AACCCGTACCTTTGGGCAGCCCCAGCTGCTGCAGTTCACTGGACAAGGATTCGCCATCGACACTG AACCCGTACCTTTGGGCAGCCCCAGCTGCTGCTGTTCACTGGACAAGGATTCGCCATCGACACTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:75339033..75339114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 7 ovary 112040 RMVar_ID_112040 Human_SNP_ID_824882821 m1A Human chr15 - 44715552 44715548 44715553 TGAAAGACAAGTCTGAATGCTCCACTTTTTCAATTCTCTCTCCATTCTTCAGTAAGTCAACTTCA TGAAAGACAAGTCTGAATGCTCCACTTTTTC_____TCTCTCCATTCTTCAGTAAGTCAACTTCA AGAATT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:44715401..44715700 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 32..36 33 STAD 2 - 112041 RMVar_ID_112041 Human_SNP_ID_824897113 m1A Human chr15 - 75617551 75617551 75617551 ATATGTCCTTATGCCTTTTTTTTCCTTCCAGCAAGCGGCTGGATTATGTGAACCATGCCAGAAGA ATATGTCCTTATGCCTTTTTTTTCCTTCCAGCTAGCGGCTGGATTATGTGAACCATGCCAGAAGA T A SNUPN Ensembl:ENSG00000169371 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:75617523..75617615 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_Splice_Rec_1628940,Human_Splice_Rec_1628956,Human_Splice_Rec_1628974,Human_Splice_Rec_1628990,Human_Splice_Rec_1629020,Human_Splice_Rec_1629032,Human_Splice_Rec_1629040,Human_Splice_Rec_1629044 RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173983,RMVar_hsa_circ_323168,RMVar_hsa_circ_294643,RMVar_hsa_circ_173987,RMVar_hsa_circ_173988,RMVar_hsa_circ_329643,RMVar_hsa_circ_349293,RMVar_hsa_circ_281110,RMVar_hsa_circ_359037,RMVar_hsa_circ_173990 112042 RMVar_ID_112042 Human_SNP_ID_824899104 m1A Human chr15 - 90232329 90232320 90232330 CTGAGAACACCGACAGTTCCCCTCTCTCTACCAGAGCCCACAGGCGGTTTTGTGAGCTGCTTCCC CTGAGAACACCGACAGTTCCCCTCTCTCTAC__________AGGCGGTTTTGTGAGCTGCTTCCC TGTGGGCTCTG T CIB1 Ensembl:ENSG00000185043 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:90232301..90232390 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..41 33 PRAD 1 - RMVar_hsa_circ_102799,RMVar_hsa_circ_85101,RMVar_hsa_circ_174747,RMVar_hsa_circ_174748 112043 RMVar_ID_112043 Human_SNP_ID_824900412 m1A Human chr15 - 65551681 65551681 65551681 AAATGCAGCACGTTTTCAGTGATGCTGATGGCAGGGTTCTGTGAAAAGAGACCAAGGATGCAAGA AAATGCAGCACGTTTTCAGTGATGCTGATGGCGGGGTTCTGTGAAAAGAGACCAAGGATGCAAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:65551676..65551725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 9 large intestine 112044 RMVar_ID_112044 Human_SNP_ID_824904425 m1A Human chr15 + 43535152 43535152 43535152 TGATGTCAGGGACCTTCTGACATGGCTGGCTGAGCGCCTCAGAAATGTCCTGGCATGGCTGGCTG TGATGTCAGGGACCTTCTGACATGGCTGGCTGGGCGCCTCAGAAATGTCCTGGCATGGCTGGCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:43535106..43535206 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine 112045 RMVar_ID_112045 Human_SNP_ID_824905745 m1A Human chr15 + 72217482 72217482 72217482 TTCCAGACTTAATCATCTCCTTCAACGTCTCCACTGATCGGGAAGCTGGGCCTATTAGGAAAAGT TTCCAGACTTAATCATCTCCTTCAACGTCTCCGCTGATCGGGAAGCTGGGCCTATTAGGAAAAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:72217356..72217556 26863196 MeRIP-seq:(Medium) rs201533100 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 8 lung 112046 RMVar_ID_112046 Human_SNP_ID_824911392 m1A Human chr15 - 66490557 66490557 66490557 TGCTGGGCTGGTTAAGGCCGATGGTGGAGCAGAGCCAACCTGCAAAATCCACTTCCTCAGCATCA TGCTGGGCTGGTTAAGGCCGATGGTGGAGCAGGGCCAACCTGCAAAATCCACTTCCTCAGCATCA T C SNAPC5,AC116913.1 Ensembl:ENSG00000174446,Ensembl:ENSG00000261351 Protein coding,lincRNA 3'UTR,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:66489253..66493475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine ulcerative_colitis 4 large intestine Human_RBP_ID_6486879 112047 RMVar_ID_112047 Human_SNP_ID_824919834 m1A Human chr15 - 89293994 89293994 89293994 TGTCTTTAAGCACTCTAGCAGAACCTTACCTGAAAAGAGCAGTGAGAAGACTGGACACAAATTTC TGTCTTTAAGCACTCTAGCAGAACCTTACCTGCAAAGAGCAGTGAGAAGACTGGACACAAATTTC T G RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:89293975..89295042 32194978 MeRIP-seq:(Medium) rs1427712731 Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_12630610 112048 RMVar_ID_112048 Human_SNP_ID_824920106 m1A Human chr15 + 89333587 89333587 89333587 CCGCCCTCCGAGGATAGCACTTGCGGCTGCTGAGGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTG CCGCCCTCCGAGGATAGCACTTGCGGCTGCTGTGGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:89333539..89333628 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 112049 RMVar_ID_112049 Human_SNP_ID_824920688 m1A Human chr15 + 80596442 80596442 80596442 GGGGGAGAAGCCCAGGACTGGGAGAATCGCACATGCCCCAGGGGTTTTCACCAAGGATTTTCAAG GGGGGAGAAGCCCAGGACTGGGAGAATCGCACGTGCCCCAGGGGTTTTCACCAAGGATTTTCAAG A G ARNT2 Ensembl:ENSG00000172379 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6495511 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_14569,GWAS_ID_14570,GWAS_ID_14571 112050 RMVar_ID_112050 Human_SNP_ID_824930789 m1A Human chr15 - 70655349 70655349 70655349 GTGGCAGGTGCCTGTAGTCCCAGGTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACCTGGGA GTGGCAGGTGCCTGTAGTCCCAGGTACTCGGGGGGCTGAGACAGGAGAATCGCTTGAACCTGGGA T C UACA Ensembl:ENSG00000137831 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs567189507 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112051 RMVar_ID_112051 Human_SNP_ID_824954416 m1A Human chr15 + 65185204 65185204 65185204 GGGGCTTCGCCCCCTGAGGACCTCCGGGTCACAGCGGCGTGAATCCTGCCCGCAAGGCGCGCTGA GGGGCTTCGCCCCCTGAGGACCTCCGGGTCACGGCGGCGTGAATCCTGCCCGCAAGGCGCGCTGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:65185158..65185350 26863196 MeRIP-seq:(Medium) rs1156856978 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112052 RMVar_ID_112052 Human_SNP_ID_824967814 m1A Human chr15 + 28163194 28163194 28163194 GGCTGCACACTGACAGCTTGAGCAGGTCTACCACCACACGAGTGTCATCCGCAATCAGCAGACTG GGCTGCACACTGACAGCTTGAGCAGGTCTACCGCCACACGAGTGTCATCCGCAATCAGCAGACTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:28163143..28163225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 KICH,kidney chromophobe_renal_cell_carcinoma 2 kidney 112053 RMVar_ID_112053 Human_SNP_ID_824974901 m1A Human chr15 - 40458649 40458649 40458649 GCACTTTGCAGGCCTTGGGCTTCTCAGGAACCAATGGGCGCTTACGAAGTGGGTAATTCTTGCGG GCACTTTGCAGGCCTTGGGCTTCTCAGGAACCGATGGGCGCTTACGAAGTGGGTAATTCTTGCGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:40458598..40459348 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 112054 RMVar_ID_112054 Human_SNP_ID_824980050 m1A Human chr15 + 93002274 93002271 93002275 GGAGAAACAAATGAGTTCTAGGAAAGACAAAGAAGGGGACAAGGAAAGAAAGAAGTCAAAAGATA GGAGAAACAAATGAGTTCTAGGAAAGACAA____GGGGACAAGGAAAGAAAGAAGTCAAAAGATA AAGAA A CHD2 Ensembl:ENSG00000173575 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:93002152..93002368 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 CLLE 1 - Human_RBP_ID_887249,Human_RBP_ID_2462184,Human_RBP_ID_3945935,Human_RBP_ID_5523558,Human_RBP_ID_9345324,Human_RBP_ID_24544186,Human_RBP_ID_26327145,Human_RBP_ID_27809960 Human_Splice_Rec_1646932,Human_Splice_Rec_1646933,Human_Splice_Rec_1647112,Human_Splice_Rec_1647113,Human_Splice_Rec_1647368,Human_Splice_Rec_1647394,Human_Splice_Rec_1647395,Human_Splice_Rec_1647414,Human_Splice_Rec_1647415 RMVar_hsa_circ_22375,RMVar_hsa_circ_98654,RMVar_hsa_circ_174984,RMVar_hsa_circ_362938,RMVar_hsa_circ_88004,RMVar_hsa_circ_63270,RMVar_hsa_circ_174987,RMVar_hsa_circ_60206,RMVar_hsa_circ_88492,RMVar_hsa_circ_175022,RMVar_hsa_circ_53788,RMVar_hsa_circ_175023,RMVar_hsa_circ_70647,RMVar_hsa_circ_19468,RMVar_hsa_circ_72524,RMVar_hsa_circ_56036,RMVar_hsa_circ_16759,RMVar_hsa_circ_365470,RMVar_hsa_circ_175038,RMVar_hsa_circ_94734,RMVar_hsa_circ_55449,RMVar_hsa_circ_74275,RMVar_hsa_circ_119721,RMVar_hsa_circ_175041,RMVar_hsa_circ_356133,RMVar_hsa_circ_103601,RMVar_hsa_circ_175048,RMVar_hsa_circ_175043,RMVar_hsa_circ_265214,RMVar_hsa_circ_283661,RMVar_hsa_circ_369031,RMVar_hsa_circ_302819,RMVar_hsa_circ_175045,RMVar_hsa_circ_175046,RMVar_hsa_circ_122989,RMVar_hsa_circ_277927,RMVar_hsa_circ_353321,RMVar_hsa_circ_364817,RMVar_hsa_circ_334097,RMVar_hsa_circ_271889,RMVar_hsa_circ_175050,RMVar_hsa_circ_175051,RMVar_hsa_circ_175049,RMVar_hsa_circ_72838,RMVar_hsa_circ_336105,RMVar_hsa_circ_352757,RMVar_hsa_circ_363894,RMVar_hsa_circ_296564 112055 RMVar_ID_112055 Human_SNP_ID_825026420 m1A Human chr15 - 66379387 66379387 66379387 CAGTTTAAAACAAGGATATCAGGAAATTTTTGAATGGTATCTATGTCTCTGAAAAAGGAACTGTT CAGTTTAAAACAAGGATATCAGGAAATTTTTGGATGGTATCTATGTCTCTGAAAAAGGAACTGTT T C RPL9P25,TIPIN Ensembl:ENSG00000240821,Ensembl:ENSG00000075131 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_17870949 Human_miRNA_ID_1867158 112056 RMVar_ID_112056 Human_SNP_ID_825034049 m1A Human chr15 - 83067023 83067023 83067023 TCTCTGGGGCCCCTGCTCCCCCTGCAGCGGGAACCTCTCTACAACTGGCAGGCGACCAAGGCGTC TCTCTGGGGCCCCTGCTCCCCCTGCAGCGGGAGCCTCTCTACAACTGGCAGGCGACCAAGGCGTC T C BTBD1 Ensembl:ENSG00000064726 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr15:83066926..83067180;chr15:83066942..83067226 26863410,26863196 MeRIP-seq:(Medium) rs774930502 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_465842,Human_RBP_ID_814520,Human_RBP_ID_4342907,Human_RBP_ID_5464330,Human_RBP_ID_17868168 112057 RMVar_ID_112057 Human_SNP_ID_825034101 m1A Human chr15 - 31503789 31503789 31503789 CAGTGTGGACAACTCTGAGGACCCCGTGTACGAGAGCCTGGAAGAGTTCCACGTTTTTGTCCTAG CAGTGTGGACAACTCTGAGGACCCCGTGTACGTGAGCCTGGAAGAGTTCCACGTTTTTGTCCTAG T A OTUD7A Ensembl:ENSG00000169918 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:31503738..31503869 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_Splice_Rec_1577156,Human_Splice_Rec_1577157 RMVar_hsa_circ_267462 112058 RMVar_ID_112058 Human_SNP_ID_825062430 m1A Human chr15 - 79311281 79311281 79311281 CGGCCCGGCGCAGGAGCAGCAGCAGAAGCAGCACGGAGGCGGAGCGCGGGACAGTGCTGCCCATG CGGCCCGGCGCAGGAGCAGCAGCAGAAGCAGCTCGGAGGCGGAGCGCGGGACAGTGCTGCCCATG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr15:79311191..79311280 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast HER-positive_carcinoma 3 breast 112059 RMVar_ID_112059 Human_SNP_ID_825063927 m1A Human chr15 - 31634511 31634511 31634511 CAGACAGAGGCATGGTGGGTGGAGACGGGTGGAGAACATCCCGGCAGAACACAGAGCACGTGCTG CAGACAGAGGCATGGTGGGTGGAGACGGGTGGGGAACATCCCGGCAGAACACAGAGCACGTGCTG T C OTUD7A Ensembl:ENSG00000169918 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:31634509..31634574 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112060 RMVar_ID_112060 Human_SNP_ID_825086383 m1A Human chr15 + 84802275 84802275 84802275 GGAAGAATGTGCCGGTGAGCCTTTGTCAGCTGACCCAGAGGCGAGGAGATTGCTGGGCCCGGCCC GGAAGAATGTGCCGGTGAGCCTTTGTCAGCTGGCCCAGAGGCGAGGAGATTGCTGGGCCCGGCCC A G ZNF592 Ensembl:ENSG00000166716 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:84802226..84802375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_277104,Human_RBP_ID_759651,Human_RBP_ID_18189600,Human_RBP_ID_22047667,Human_RBP_ID_23672045 112061 RMVar_ID_112061 Human_SNP_ID_825113754 m1A Human chr15 - 43330477 43330477 43330477 TTCCTGAGTCTCTTCTGGCCATGGGCCCCCGGAGCCGTGAGCGTCGGGCAGGCGCGGTACAGAAC TTCCTGAGTCTCTTCTGGCCATGGGCCCCCGGGGCCGTGAGCGTCGGGCAGGCGCGGTACAGAAC T C LCMT2 Ensembl:ENSG00000168806 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:43330430..43330582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach Human_RBP_ID_4322325 Human_Splice_Rec_1592349 112062 RMVar_ID_112062 Human_SNP_ID_825117498 m1A Human chr15 - 40462231 40462231 40462231 CCAACAGGTACCCAGCCATTAGTGCGGCGGCGACGGCGGCGGCGAGGGCGTGGGCGCTGGACACG CCAACAGGTACCCAGCCATTAGTGCGGCGGCGGCGGCGGCGGCGAGGGCGTGGGCGCTGGACACG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40461990..40462234 26863196 MeRIP-seq:(Medium) rs762888298 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 BRCA,HNSC,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 8 head and neck,large intestine 112063 RMVar_ID_112063 Human_SNP_ID_825148314 m1A Human chr15 - 78149427 78149427 78149427 CTGCCACACGCCGGCCTGCCAGCGCTCACCTTAGAGATCCACGCGGGCCCAGCCATCGCTTCCCC CTGCCACACGCCGGCCTGCCAGCGCTCACCTTGGAGATCCACGCGGGCCCAGCCATCGCTTCCCC T C lnc-ACSBG1-3 RNACentral:URS00008BFDDE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr15:78149376..78149536;chr15:78149414..78149639;chr15:78149418..78149654 26863196 MeRIP-seq:(Medium) rs11555541 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,colon adenocarcinoma,COCA,rectum adenocarcinoma,mouth squamous_cell_carcinoma,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 74 caecum,liver,head and neck,large intestine 112064 RMVar_ID_112064 Human_SNP_ID_825162348 m1A Human chr15 + 38454195 38454195 38454195 TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGATGGAGGGAGACGTGCTGGACACACTGGAGGCG TGAGAGGGCCGGAGCCGGGTCCCCAACCGACGGTGGAGGGAGACGTGCTGGACACACTGGAGGCG A G FAM98B Ensembl:ENSG00000171262 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr15:38454144..38464108 26863196 MeRIP-seq:(Medium) rs750510877 Functional Loss SNV ICGC 33..33 33 PEME 1 - Human_RBP_ID_456325,Human_RBP_ID_4318686,Human_RBP_ID_6421050,Human_RBP_ID_18661780 Human_Splice_Rec_1582357,Human_Splice_Rec_1582371 112065 RMVar_ID_112065 Human_SNP_ID_825195055 m1A Human chr15 + 74036235 74036235 74036235 AAGAAACTTCTGTCACCCTTGCACTCTCCTGTATTCTGAGTCCCTGGCCAATAGCACAGCCTTCC AAGAAACTTCTGTCACCCTTGCACTCTCCTGTGTTCTGAGTCCCTGGCCAATAGCACAGCCTTCC A G PML Ensembl:ENSG00000140464 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9479 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 13 large intestine Human_RBP_ID_12588274,Human_RBP_ID_17077044,Human_RBP_ID_18938326,Human_RBP_ID_26435877 GWAS_ID_12758,GWAS_ID_12759,GWAS_ID_12760,GWAS_ID_12761,GWAS_ID_12762,GWAS_ID_12763,GWAS_ID_12764,GWAS_ID_12765,GWAS_ID_12766,GWAS_ID_12767,GWAS_ID_12768,GWAS_ID_12769,GWAS_ID_12770,GWAS_ID_12771,GWAS_ID_12772,GWAS_ID_12773,GWAS_ID_12774 RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 112066 RMVar_ID_112066 Human_SNP_ID_825239744 m1A Human chr15 - 69452893 69452893 69452893 CGCTGCCGGACGCGGTGCTAGTCGCCGGATGAAGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT CGCTGCCGGACGCGGTGCTAGTCGCCGGATGACGTGAGGGCCTCACCCCAACGCAGCCTTAGCTT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:69452826..69453230 32194978 MeRIP-seq:(Medium) rs552626514 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 112067 RMVar_ID_112067 Human_SNP_ID_825247788 m1A Human chr15 - 67184799 67184799 67184799 AGCCATAGCGCTGGTTACAGTTGGGAGACTGGACAAAAATAGCGCTGTCACTGAGGCACTCTGCG AGCCATAGCGCTGGTTACAGTTGGGAGACTGGCCAAAAATAGCGCTGTCACTGAGGCACTCTGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:67181246..67186715 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 8 large intestine 112068 RMVar_ID_112068 Human_SNP_ID_825249064 m1A Human chr15 - 80989634 80989632 80989635 CGAGTCTACCCCACCTCCCCGGAAGAAGAAGAAGGATATTCGCGATTACAATGATGCAGACATGG CGAGTCTACCCCACCTCCCCGGAAGAAGAAG___GATATTCGCGATTACAATGATGCAGACATGG CCTT C MESD Ensembl:ENSG00000117899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:80989528..80989828 26863196 MeRIP-seq:(Medium) rs756097775 Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_1835652,Human_RBP_ID_4348204,Human_RBP_ID_9371199,Human_RBP_ID_18669862,Human_RBP_ID_22759451 Human_Splice_Rec_1634551,Human_Splice_Rec_1634559,Human_Splice_Rec_1634567,Human_Splice_Rec_1634581,Human_Splice_Rec_1634585 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 112069 RMVar_ID_112069 Human_SNP_ID_825256409 m1A Human chr15 + 88467994 88467994 88467994 CCAAGACGCTGCGGCCAAGCAGAAAGTTGAACAGAACGCGGCTCCCAGCCACACCAAGTTCAGGT CCAAGACGCTGCGGCCAAGCAGAAAGTTGAACGGAACGCGGCTCCCAGCCACACCAAGTTCAGGT A G MRPS11 Ensembl:ENSG00000181991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:88467901..88468073 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4338117,Human_RBP_ID_12627614,Human_RBP_ID_19067556 Human_Splice_Rec_1640652,Human_Splice_Rec_1640653,Human_Splice_Rec_1640662,Human_Splice_Rec_1640664,Human_Splice_Rec_1640665,Human_Splice_Rec_1640672,Human_Splice_Rec_1640682,Human_Splice_Rec_1640683,Human_Splice_Rec_1640686,Human_Splice_Rec_1640687,Human_Splice_Rec_1640696,Human_Splice_Rec_1640697,Human_Splice_Rec_1640703,Human_Splice_Rec_1640711 RMVar_hsa_circ_31117 112070 RMVar_ID_112070 Human_SNP_ID_825269404 m1A Human chr15 - 48878297 48878297 48878297 CTGTTGGGCCCCGCTGCGGGAGGGACGCAGGGATAGCTCCCGGCTCCCGCTGCCTACCTCCATCT CTGTTGGGCCCCGCTGCGGGAGGGACGCAGGGCTAGCTCCCGGCTCCCGCTGCCTACCTCCATCT T G SHC4 Ensembl:ENSG00000185634 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr15:48878250..48878425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 112071 RMVar_ID_112071 Human_SNP_ID_825287232 m1A Human chr15 - 101274639 101274639 101274639 AAAAAAGGAGACAGAAGATTGAAATGTGGGACAGCATGCAAGAAGGAAAAAGTTACAAAGGAAAT AAAAAAGGAGACAGAAGATTGAAATGTGGGACCGCATGCAAGAAGGAAAAAGTTACAAAGGAAAT T G SELENOS Ensembl:ENSG00000131871 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:101274492..101274721 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_455072,Human_RBP_ID_886082,Human_RBP_ID_1503283,Human_RBP_ID_1827649,Human_RBP_ID_2434534,Human_RBP_ID_6413011,Human_RBP_ID_9048816,Human_RBP_ID_9371334,Human_RBP_ID_18411281,Human_RBP_ID_23645543,Human_RBP_ID_24544241,Human_RBP_ID_26327173,Human_RBP_ID_27809980 Human_Splice_Rec_1651198,Human_Splice_Rec_1651199,Human_Splice_Rec_1651210,Human_Splice_Rec_1651211,Human_Splice_Rec_1651219,Human_Splice_Rec_1651228,Human_Splice_Rec_1651229,Human_Splice_Rec_1651238,Human_Splice_Rec_1651239,Human_Splice_Rec_1651248 RMVar_hsa_circ_81892,RMVar_hsa_circ_91652,RMVar_hsa_circ_175222,RMVar_hsa_circ_175223,RMVar_hsa_circ_363651 112072 RMVar_ID_112072 Human_SNP_ID_825299789 m1A Human chr15 + 58717726 58717726 58717726 CTGATATATTTATTTAAAGGATTCCCATACTGACCTATAAAAAAAAAACAACATTCTGAATTAGT CTGATATATTTATTTAAAGGATTCCCATACTGTCCTATAAAAAAAAAACAACATTCTGAATTAGT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:58717687..58717785 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 112073 RMVar_ID_112073 Human_SNP_ID_825314393 m1A Human chr15 + 41417253 41417253 41417253 AGCCGGGGGACCACCATGGTAAAGAAGCGGAAAGGCCGCGTCGTGATCGACTCGGACACAGAGGA AGCCGGGGGACCACCATGGTAAAGAAGCGGAAGGGCCGCGTCGTGATCGACTCGGACACAGAGGA A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:41417134..41417300 26863196 MeRIP-seq:(Medium) rs1210479028 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_759955,Human_RBP_ID_4342596,Human_RBP_ID_5566307,Human_RBP_ID_8804051,Human_RBP_ID_9370750,Human_RBP_ID_18418339,Human_RBP_ID_26326318,Human_RBP_ID_27810112 Human_Splice_Rec_1586735,Human_Splice_Rec_1586767 112074 RMVar_ID_112074 Human_SNP_ID_825332646 m1A Human chr15 - 73942964 73942964 73942964 CCCAACACTCTACACTTCTGCCTCAGCTCCTTACCTGGCCAGACACTTCTCCTCCGCAGCACAGC CCCAACACTCTACACTTCTGCCTCAGCTCCTTGCCTGGCCAGACACTTCTCCTCCGCAGCACAGC T C LOXL1-AS1,LOXL1-AS1:2,LOXL1-AS1:3 RNACentral:URS0000D5B0A7,RNACentral:URS0000D58EE7,RNACentral:URS0000D56F66 lincRNA,lincRNA,lincRNA exon,exon,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr15:73942914..73947081 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 2 oesophagus 112075 RMVar_ID_112075 Human_SNP_ID_825336750 m1A Human chr15 - 44715435 44715435 44715435 CATTCTCTGCTGGATGACGTGAGTAAACCTGAATCTTTGGAGTACCTGAGGAATATCGGGAAAAG CATTCTCTGCTGGATGACGTGAGTAAACCTGAGTCTTTGGAGTACCTGAGGAATATCGGGAAAAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:44715426..44715450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 112076 RMVar_ID_112076 Human_SNP_ID_825336753 m1A Human chr15 - 44715435 44715435 44715435 CATTCTCTGCTGGATGACGTGAGTAAACCTGAATCTTTGGAGTACCTGAGGAATATCGGGAAAAG CATTCTCTGCTGGATGACGTGAGTAAACCTGATTCTTTGGAGTACCTGAGGAATATCGGGAAAAG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr15:44715426..44715450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 112077 RMVar_ID_112077 Human_SNP_ID_825400279 m1A Human chr15 - 84687751 84687751 84687751 CCCTTCCAGTGGCAGCATGGAACCTGCATTTCATAGAGGAGATCTTCTCTTTCTAACAAATCGAG CCCTTCCAGTGGCAGCATGGAACCTGCATTTCGTAGAGGAGATCTTCTCTTTCTAACAAATCGAG T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:84687701..84687775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_466131,Human_RBP_ID_1510068,Human_RBP_ID_3486001,Human_RBP_ID_4337565,Human_RBP_ID_18670390,Human_RBP_ID_23208985,Human_RBP_ID_23671894,Human_RBP_ID_25188860 Human_Splice_Rec_1638534,Human_Splice_Rec_1638542,Human_Splice_Rec_1638554,Human_Splice_Rec_1638564,Human_Splice_Rec_1638576,Human_Splice_Rec_1638586,Human_Splice_Rec_1638600 RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_77057,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_300525,RMVar_hsa_circ_174461,RMVar_hsa_circ_277529,RMVar_hsa_circ_174464,RMVar_hsa_circ_174462,RMVar_hsa_circ_174463,RMVar_hsa_circ_301010,RMVar_hsa_circ_363353 112078 RMVar_ID_112078 Human_SNP_ID_825405273 m1A Human chr15 - 40955518 40955518 40955518 TCTGTGGGGTGGCCACATAGGCCAATGCCTTCAGTGGTTGGTCAGGAGCATCTTGGGGATAGAAG TCTGTGGGGTGGCCACATAGGCCAATGCCTTCGGTGGTTGGTCAGGAGCATCTTGGGGATAGAAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:40955467..40955640 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine 112079 RMVar_ID_112079 Human_SNP_ID_825422900 m1A Human chr15 - 66503362 66503362 66503362 AACAACAGACAGCCCTATGCTGTCAGTGAATTAGCAGGTATGGATTTATATCTTCTGCAGATATT AACAACAGACAGCCCTATGCTGTCAGTGAATTTGCAGGTATGGATTTATATCTTCTGCAGATATT T A RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:66503006..66503395 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_886580,Human_RBP_ID_1832364,Human_RBP_ID_17252013,Human_RBP_ID_22799054,Human_RBP_ID_23208930,Human_RBP_ID_26933085,Human_RBP_ID_27233063 Human_Splice_Rec_1616057,Human_Splice_Rec_1616075,Human_Splice_Rec_1616093,Human_Splice_Rec_1616111,Human_Splice_Rec_1616127,Human_Splice_Rec_1616153,Human_Splice_Rec_1616163,Human_Splice_Rec_1616171,Human_Splice_Rec_1616179,Human_Splice_Rec_1616187 RMVar_hsa_circ_82571,RMVar_hsa_circ_70834,RMVar_hsa_circ_173307,RMVar_hsa_circ_113031,RMVar_hsa_circ_173314,RMVar_hsa_circ_34075,RMVar_hsa_circ_100348,RMVar_hsa_circ_173320 112080 RMVar_ID_112080 Human_SNP_ID_825423037 m1A Human chr15 + 56465017 56465017 56465017 AAAATACCCCCTCTCGTGGGACCGCGGCCACCACCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC AAAATACCCCCTCTCGTGGGACCGCGGCCACCCCCTCCCGCCGCAAACGCAGCAGCCAGCAGCCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:56464927..56465075 26863196 MeRIP-seq:(Medium) rs755806825 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue 112081 RMVar_ID_112081 Human_SNP_ID_825425572 m1A Human chr15 - 66503166 66503166 66503166 AGCAGCTACAACTTTTATCTCTTCTCAATTTTAGGTCATCAGACTAGTGCTGAGTCTTGGGGTAC AGCAGCTACAACTTTTATCTCTTCTCAATTTTTGGTCATCAGACTAGTGCTGAGTCTTGGGGTAC T A RPL4 Ensembl:ENSG00000174444 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr15:66503149..66503359 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_461829,Human_RBP_ID_886579,Human_RBP_ID_2451244,Human_RBP_ID_5274576,Human_RBP_ID_6451437,Human_RBP_ID_8082504,Human_RBP_ID_9055315,Human_RBP_ID_12562853,Human_RBP_ID_17000201,Human_RBP_ID_17864643,Human_RBP_ID_18281316,Human_RBP_ID_23273216,Human_RBP_ID_25156224,Human_RBP_ID_26633412 RMVar_hsa_circ_82571,RMVar_hsa_circ_70834,RMVar_hsa_circ_173307,RMVar_hsa_circ_113031,RMVar_hsa_circ_173314,RMVar_hsa_circ_34075,RMVar_hsa_circ_100348,RMVar_hsa_circ_173320 112082 RMVar_ID_112082 Human_SNP_ID_825428152 m1A Human chr15 + 78787909 78787909 78787909 CTCCCGCTCCTTTACCGCTACAGGCCTTTCTCAGGCTTCCTCTACCAAGAACACCATTCTTCTCC CTCCCGCTCCTTTACCGCTACAGGCCTTTCTCGGGCTTCCTCTACCAAGAACACCATTCTTCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:78787900..78788016 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112083 RMVar_ID_112083 Human_SNP_ID_825434844 m1A Human chr15 + 44537223 44537223 44537223 CGAGATGGCGGCGGCGGCGGCGGCGGCGGGGGACTCGGACTCCTGGGGTGAGGAGAAGTTGCTGG CGAGATGGCGGCGGCGGCGGCGGCGGCGGGGGGCTCGGACTCCTGGGGTGAGGAGAAGTTGCTGG A G EIF3J Ensembl:ENSG00000104131 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr15:44537126..44537450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,COCA,large_intestine adenocarcinoma 7 ovary,large intestine Human_RBP_ID_232541,Human_RBP_ID_4342643,Human_RBP_ID_9324254,Human_RBP_ID_22934714,Human_RBP_ID_27435356 Human_Splice_Rec_1595507,Human_Splice_Rec_1595517,Human_Splice_Rec_1595531 112084 RMVar_ID_112084 Human_SNP_ID_825437145 m1A Human chr15 + 64093720 64093720 64093720 GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCACAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC GGCAGCTCCCGGCTCAGAGAGGCCGGAGAGCCTCAGGACTCTGCTCAGCGTCCAGGAGAGCAGCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:64093670..64093770 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain 112085 RMVar_ID_112085 Human_SNP_ID_825452586 m1A Human chr15 - 100786385 100786383 100786385 TCACACACACATACACACGCACACTCACACACACGACACACACTCACACACATTCACACACATAA TCACACACACATACACACGCACACTCACACAC__GACACACACTCACACACATTCACACACATAA CGT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:100786166..100786441 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 PBCA 1 - 112086 RMVar_ID_112086 Human_SNP_ID_825456821 m1A Human chr15 + 74409761 74409761 74409761 CCGTTTCCCTCACCCCACCCCCTCCCATAACCACCCCCAACACTAGGGGCTCCAACAACGTCCCC CCGTTTCCCTCACCCCACCCCCTCCCATAACCCCCCCCAACACTAGGGGCTCCAACAACGTCCCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr15:74409710..74409891 26863196 MeRIP-seq:(Medium) rs1481070852 Functional Loss SNV ICGC 33..33 33 MALY 1 - 112087 RMVar_ID_112087 Human_SNP_ID_825460292 m1A Human chr15 + 90228586 90228586 90228586 AGCATCCAAGACAGCTTCGTGGAGGTATCCCCAGTGTGCCCCCGGCCCCGGGTCCGCCTTGGCTC AGCATCCAAGACAGCTTCGTGGAGGTATCCCCCGTGTGCCCCCGGCCCCGGGTCCGCCTTGGCTC A C SEMA4B Ensembl:ENSG00000185033 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr15:90228537..90228608 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_22440187 RMVar_hsa_circ_107082,RMVar_hsa_circ_174742 112088 RMVar_ID_112088 Human_SNP_ID_825467089 m1A Human chr15 - 45156825 45156825 45156825 GCCGATGAGAAACCCAGGGGAGGGTGAAGGGAACATGAGAAGGGAGGCAACATGGAGAGAGGGAG GCCGATGAGAAACCCAGGGGAGGGTGAAGGGACCATGAGAAGGGAGGCAACATGGAGAGAGGGAG T G AC051619.5 Ensembl:ENSG00000259539 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr15:45156774..45156883 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 112089 RMVar_ID_112089 Human_SNP_ID_825504489 m1A Human chr15 + 90970428 90970428 90970428 ATACTAACCTTGCTGCCAGAAGGAGGAAGTCGAGACACGGGGGAGTGGTAGACTGTCCCTCCAAA ATACTAACCTTGCTGCCAGAAGGAGGAAGTCGTGACACGGGGGAGTGGTAGACTGTCCCTCCAAA A T PRC1-AS1 Ensembl:ENSG00000258725 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr15:90966236..90974059 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_5568079 112090 RMVar_ID_112090 Human_SNP_ID_844009990 m1A Human chr22 + 37241642 37241642 37241642 AAAGGCGTTGGTGGTGTAGCTGATGAGAAGGCAGGTCTTGCCCACGGCCCTGAAAGACAGGAAGT AAAGGCGTTGGTGGTGTAGCTGATGAGAAGGCGGGTCTTGCCCACGGCCCTGAAAGACAGGAAGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37241553..37241710 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 112091 RMVar_ID_112091 Human_SNP_ID_844013986 m1A Human chr22 + 31754887 31754887 31754887 GTGGCAGGGAGGCAAGATGACTTCTCTGCCCCAAGCTTGGAACAGCTAAAGGGAAAAACAGTGCA GTGGCAGGGAGGCAAGATGACTTCTCTGCCCCCAGCTTGGAACAGCTAAAGGGAAAAACAGTGCA A C DEPDC5 Ensembl:ENSG00000100150 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31753895..31754949 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 19 kidney Human_Splice_Rec_2156832,Human_Splice_Rec_2156833,Human_Splice_Rec_2156910,Human_Splice_Rec_2156911,Human_Splice_Rec_2156956,Human_Splice_Rec_2156957,Human_Splice_Rec_2157006,Human_Splice_Rec_2157007,Human_Splice_Rec_2157090,Human_Splice_Rec_2157091,Human_Splice_Rec_2157172,Human_Splice_Rec_2157173,Human_Splice_Rec_2157252,Human_Splice_Rec_2157253,Human_Splice_Rec_2157268,Human_Splice_Rec_2157269,Human_Splice_Rec_2157280,Human_Splice_Rec_2157281,Human_Splice_Rec_2157360,Human_Splice_Rec_2157361,Human_Splice_Rec_2157442,Human_Splice_Rec_2157443,Human_Splice_Rec_2157522,Human_Splice_Rec_2157523,Human_Splice_Rec_2157564,Human_Splice_Rec_2157565,Human_Splice_Rec_2157644,Human_Splice_Rec_2157646,Human_Splice_Rec_2157647,Human_Splice_Rec_2157730,Human_Splice_Rec_2157731,Human_Splice_Rec_2157770,Human_Splice_Rec_2157771,Human_Splice_Rec_2157852,Human_Splice_Rec_2157853,Human_Splice_Rec_2157934,Human_Splice_Rec_2157935,Human_Splice_Rec_2158018,Human_Splice_Rec_2158019,Human_Splice_Rec_2158032,Human_Splice_Rec_2158033,Human_Splice_Rec_2158110,Human_Splice_Rec_2158111,Human_Splice_Rec_2158190,Human_Splice_Rec_2158191,Human_Splice_Rec_2158272,Human_Splice_Rec_2158273,Human_Splice_Rec_2158354,Human_Splice_Rec_2158355,Human_Splice_Rec_2158436,Human_Splice_Rec_2158437,Human_Splice_Rec_2158478,Human_Splice_Rec_2158479,Human_Splice_Rec_2158562,Human_Splice_Rec_2158563,Human_Splice_Rec_2158578,Human_Splice_Rec_2158579,Human_Splice_Rec_2158658,Human_Splice_Rec_2158659,Human_Splice_Rec_2158700,Human_Splice_Rec_2158701,Human_Splice_Rec_2158782,Human_Splice_Rec_2158783,Human_Splice_Rec_2158830,Human_Splice_Rec_2158831,Human_Splice_Rec_2158910,Human_Splice_Rec_2158911,Human_Splice_Rec_2158986,Human_Splice_Rec_2158987,Human_Splice_Rec_2159067,Human_Splice_Rec_2159105,Human_Splice_Rec_2159185,Human_Splice_Rec_2159691 RMVar_hsa_circ_18781,RMVar_hsa_circ_47860 112092 RMVar_ID_112092 Human_SNP_ID_844015968 m1A Human chr22 + 17107754 17107754 17107754 TCCAGGGCCTGGAAGTGAAAAATACAGTGATGACACCAAATACACCGGTCAGTATTTCCTGGTTT TCCAGGGCCTGGAAGTGAAAAATACAGTGATGGCACCAAATACACCGGTCAGTATTTCCTGGTTT A G IL17RA Ensembl:ENSG00000177663 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17104766..17109854 32194978 MeRIP-seq:(Medium) rs150618101 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_2134142,Human_Splice_Rec_2134143,Human_Splice_Rec_2134166,Human_Splice_Rec_2134167 RMVar_hsa_circ_91856,RMVar_hsa_circ_212816 112093 RMVar_ID_112093 Human_SNP_ID_844021585 m1A Human chr22 + 37940832 37940832 37940832 CAAGAGCAAGTCCCCCAGAGACAAGAGCTAACAGCACGAGAAGCCAGTTGGGGACTGCCCCCTCC CAAGAGCAAGTCCCCCAGAGACAAGAGCTAACGGCACGAGAAGCCAGTTGGGGACTGCCCCCTCC A G MICALL1 Ensembl:ENSG00000100139 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37940782..37941281 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_579783,Human_RBP_ID_1611238,Human_RBP_ID_9392355,Human_RBP_ID_27307744 RMVar_hsa_circ_120352,RMVar_hsa_circ_214248 112094 RMVar_ID_112094 Human_SNP_ID_844035835 m1A Human chr22 - 50278660 50278660 50278660 GCGTCCGGGCTCCACAGCGCAGATCCTGTCGGACCTGGACCTGACGTCACAGCGGGAGGGCCGGT GCGTCCGGGCTCCACAGCGCAGATCCTGTCGGGCCTGGACCTGACGTCACAGCGGGAGGGCCGGT T C PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50278576..50278700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_65643,Human_RBP_ID_8865351,Human_RBP_ID_22454781 Human_Splice_Rec_2179804,Human_Splice_Rec_2179805,Human_Splice_Rec_2179844,Human_Splice_Rec_2179845,Human_Splice_Rec_2179916,Human_Splice_Rec_2179917,Human_Splice_Rec_2179988,Human_Splice_Rec_2179989,Human_Splice_Rec_2180020,Human_Splice_Rec_2180021,Human_Splice_Rec_2180046,Human_Splice_Rec_2180047,Human_Splice_Rec_2180057 RMVar_hsa_circ_84415,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_97641,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267,RMVar_hsa_circ_215268 112095 RMVar_ID_112095 Human_SNP_ID_844044503 m1A Human chr22 - 36476797 36476797 36476797 GCCGAGGTTAGAGAAGATGGTGGCCAAGCAGCACGGGAAGGTGGTGATGGCCAAGGTGGATATTG GCCGAGGTTAGAGAAGATGGTGGCCAAGCAGCGCGGGAAGGTGGTGATGGCCAAGGTGGATATTG T C TXN2 Ensembl:ENSG00000100348 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36476696..36476884 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_579237,Human_RBP_ID_17989210,Human_RBP_ID_23946057 Human_Splice_Rec_2162590,Human_Splice_Rec_2162591,Human_Splice_Rec_2162596,Human_Splice_Rec_2162597,Human_Splice_Rec_2162602,Human_Splice_Rec_2162603,Human_Splice_Rec_2162608,Human_Splice_Rec_2162609,Human_Splice_Rec_2162614,Human_Splice_Rec_2162615 Human_miRNA_ID_2172669 RMVar_hsa_circ_108869,RMVar_hsa_circ_88075,RMVar_hsa_circ_124335,RMVar_hsa_circ_107069,RMVar_hsa_circ_214109,RMVar_hsa_circ_214110,RMVar_hsa_circ_214111,RMVar_hsa_circ_334445,RMVar_hsa_circ_317084,RMVar_hsa_circ_214112,RMVar_hsa_circ_214113,RMVar_hsa_circ_214114 112096 RMVar_ID_112096 Human_SNP_ID_844044584 m1A Human chr22 - 31345634 31345634 31345634 TGCTGAGGGGAAGGGAGGGGGCGGGCAGGTGCAGCGGCCGGGCTAGTGGGAGGGGGCGGCGGCCA TGCTGAGGGGAAGGGAGGGGGCGGGCAGGTGCCGCGGCCGGGCTAGTGGGAGGGGGCGGCGGCCA T G PATZ1 Ensembl:ENSG00000100105 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:31345241..31345882;chr22:31345257..31345932 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_833601,Human_RBP_ID_5149489,Human_RBP_ID_18463940,Human_RBP_ID_19007899,Human_RBP_ID_22087146,Human_RBP_ID_22725114 RMVar_hsa_circ_79834,RMVar_hsa_circ_213800 112097 RMVar_ID_112097 Human_SNP_ID_844045299 m1A Human chr22 - 41339916 41339916 41339916 GCAGTGGGCTGGAGACAGGGATGGAGCCACCCACCACAGGTGGTAGCAGTGGGGTCCCGCCGGGG GCAGTGGGCTGGAGACAGGGATGGAGCCACCCTCCACAGGTGGTAGCAGTGGGGTCCCGCCGGGG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:41339865..41340153 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - RMVar_hsa_circ_214651 112098 RMVar_ID_112098 Human_SNP_ID_844052592 m1A Human chr22 + 37608883 37608883 37608883 CCGGTGGCGGATGGAGCCCGCGATGGAGCCGGAGACTCTGGAGGCGCGAATCAGTGAGTGTCCGG CCGGTGGCGGATGGAGCCCGCGATGGAGCCGGTGACTCTGGAGGCGCGAATCAGTGAGTGTCCGG A T GGA1 Ensembl:ENSG00000100083 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37608843..37608943 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_4708198,Human_RBP_ID_19009126,Human_RBP_ID_23015421 Human_Splice_Rec_2164091,Human_Splice_Rec_2164121,Human_Splice_Rec_2164125,Human_Splice_Rec_2164133,Human_Splice_Rec_2164165,Human_Splice_Rec_2164177 112099 RMVar_ID_112099 Human_SNP_ID_844057507 m1A Human chr22 - 28800347 28800347 28800347 AGGCAGCGAGCGGGGGGCTGCCCCAGGCGCGCAAGCGACAGCGCCTCACGCACCTGAGCCCCGAG AGGCAGCGAGCGGGGGGCTGCCCCAGGCGCGCGAGCGACAGCGCCTCACGCACCTGAGCCCCGAG T C XBP1 Ensembl:ENSG00000100219 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:28800301..28800550;chr22:28800122..28800575;chr22:28800123..28800600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_245861,Human_RBP_ID_4690749,Human_RBP_ID_5149177,Human_RBP_ID_8865912 Human_Splice_Rec_2150043,Human_Splice_Rec_2150051,Human_Splice_Rec_2150061,Human_Splice_Rec_2150077,Human_Splice_Rec_2150085 RMVar_hsa_circ_100890,RMVar_hsa_circ_213581 112100 RMVar_ID_112100 Human_SNP_ID_844062209 m1A Human chr22 + 20862433 20862433 20862433 GACAGGAAAATATGCAAATGCACTGGCCCAGCAACAGAGCTCCTGGGTCCAGAGGAGGGACATGA GACAGGAAAATATGCAAATGCACTGGCCCAGCTACAGAGCTCCTGGGTCCAGAGGAGGGACATGA A T SNAP29 Ensembl:ENSG00000099940 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20862428..20862587 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_112623,RMVar_hsa_circ_213126 112101 RMVar_ID_112101 Human_SNP_ID_844064945 m1A Human chr22 + 17980736 17980734 17980736 ACTCCAGCCACACCCACTTTCTCCAGAGTGCCACAGTTTCCGTCTTATCATTCCGCCCGTCTTAT ACTCCAGCCACACCCACTTTCTCCAGAGTGC__CAGTTTCCGTCTTATCATTCCGCCCGTCTTAT CCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:17980734..17980934 26863196 MeRIP-seq:(Medium) rs755969657 Functional Loss DEL ICGC 32..33 33 ESCA 1 - 112102 RMVar_ID_112102 Human_SNP_ID_844070518 m1A Human chr22 - 20551450 20551450 20551450 TCTCGAAAATGGATAATGAGCCTGGCCACGAGAGAAAGGTATTCGTCCTAAAAGTAAAAACAGGA TCTCGAAAATGGATAATGAGCCTGGCCACGAGTGAAAGGTATTCGTCCTAAAAGTAAAAACAGGA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20551445..20551546 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 112103 RMVar_ID_112103 Human_SNP_ID_844070639 m1A Human chr22 - 45577069 45577069 45577069 CATGCCGTCCATGTAACGCTTGATGATGTCAAAAGAGTCCCGCAGGTTCCCTTCCGTGATGTCGA CATGCCGTCCATGTAACGCTTGATGATGTCAATAGAGTCCCGCAGGTTCCCTTCCGTGATGTCGA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:45577018..45577916 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 112104 RMVar_ID_112104 Human_SNP_ID_844070917 m1A Human chr22 + 37019851 37019851 37019851 CGCCGCGCCGCGGGGGCCATGGCGGAGCCAGGAAGCCGGGAGTCCGAGACCCGGGTAACTGCCGC CGCCGCGCCGCGGGGGCCATGGCGGAGCCAGGCAGCCGGGAGTCCGAGACCCGGGTAACTGCCGC A C MPST Ensembl:ENSG00000128309 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37019801..37019945 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_246685,Human_RBP_ID_782377,Human_RBP_ID_4708184,Human_RBP_ID_9432881 Human_Splice_Rec_2163197,Human_Splice_Rec_2163203,Human_Splice_Rec_2163213 112105 RMVar_ID_112105 Human_SNP_ID_844075276 m1A Human chr22 - 28772767 28772767 28772767 CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCAAAACCCGCCAGCCTCGGATCCCGCTCTCGACC CAGGCCCGGCAGCCGCAGCCACAGCTACTGCCGAAACCCGCCAGCCTCGGATCCCGCTCTCGACC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:28772717..28772842 26863196 MeRIP-seq:(Medium) rs11556025 Functional Loss SNV ICGC 33..33 33 LUSC 2 - 112106 RMVar_ID_112106 Human_SNP_ID_844081164 m1A Human chr22 - 29789027 29789027 29789027 GAACCATGGCCGACCGCAAGAGGAGCAAAGGCATGATCCCATCCTGAGACCTGGTGCAGGGCCAG GAACCATGGCCGACCGCAAGAGGAGCAAAGGCGTGATCCCATCCTGAGACCTGGTGCAGGGCCAG T C ASCC2 Ensembl:ENSG00000100325 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29788976..29789121 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 112107 RMVar_ID_112107 Human_SNP_ID_844084169 m1A Human chr22 - 30580122 30580122 30580122 GGACAAATCTTTGTGCATTGGGGCCACCTATGACGTCACAGACTCCCGCATCACCCATCAGATTG GGACAAATCTTTGTGCATTGGGGCCACCTATGTCGTCACAGACTCCCGCATCACCCATCAGATTG T A PES1 Ensembl:ENSG00000100029 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30580038..30580200 26863196 MeRIP-seq:(Medium) rs140230829 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_RBP_ID_64947,Human_RBP_ID_1028953,Human_RBP_ID_1201297,Human_RBP_ID_3671106,Human_RBP_ID_7074488,Human_RBP_ID_8548409,Human_RBP_ID_8862659,Human_RBP_ID_9392175,Human_RBP_ID_14453639,Human_RBP_ID_17984578 Human_Splice_Rec_2153940,Human_Splice_Rec_2153941,Human_Splice_Rec_2153972,Human_Splice_Rec_2153973,Human_Splice_Rec_2154010,Human_Splice_Rec_2154011,Human_Splice_Rec_2154040,Human_Splice_Rec_2154041,Human_Splice_Rec_2154068,Human_Splice_Rec_2154069 RMVar_hsa_circ_89543,RMVar_hsa_circ_117272,RMVar_hsa_circ_29528,RMVar_hsa_circ_44901,RMVar_hsa_circ_213751,RMVar_hsa_circ_79229,RMVar_hsa_circ_213752,RMVar_hsa_circ_213750,RMVar_hsa_circ_51657 112108 RMVar_ID_112108 Human_SNP_ID_844090616 m1A Human chr22 + 41205381 41205381 41205381 GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTATTGAGGTGAGAAGGCGAGGACTTAGCGTGACT GAAACTGAGGTCTCATGGAGAAGCCCCGGAGTGTTGAGGTGAGAAGGCGAGGACTTAGCGTGACT A G L3MBTL2 Ensembl:ENSG00000100395 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:41205342..41205444;chr22:41205340..41205452 26863196 MeRIP-seq:(Medium) rs3804097 Functional Loss SNV ICGC,COSMIC 33..33 33 LUSC,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_246062,Human_RBP_ID_4708682,Human_RBP_ID_19113495 Human_Splice_Rec_2170337,Human_Splice_Rec_2170363,Human_Splice_Rec_2170371,Human_Splice_Rec_2170401,Human_Splice_Rec_2170405,Human_Splice_Rec_2170437,Human_Splice_Rec_2170465 RMVar_hsa_circ_107484,RMVar_hsa_circ_214598 112109 RMVar_ID_112109 Human_SNP_ID_844091704 m1A Human chr22 - 50201099 50201099 50201099 GTAGAGCGGGGCGCCGGCGACGGGGAACAGCGACCGAGGGGCAAGAGTCGGGCAGCCGCGAGCGA GTAGAGCGGGGCGCCGGCGACGGGGAACAGCGGCCGAGGGGCAAGAGTCGGGCAGCCGCGAGCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:50201064..50201197 26863196 MeRIP-seq:(Medium) rs5771226 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ER-positive_carcinoma,COCA,large_intestine adenocarcinoma 8 large intestine,breast 112110 RMVar_ID_112110 Human_SNP_ID_844092442 m1A Human chr22 - 46095919 46095919 46095919 GGGCTGGGACCACCCCAATGCCCTCACCTGCCACCCTGGGCTGGCTGGGACCACCCTAATGCCCT GGGCTGGGACCACCCCAATGCCCTCACCTGCCGCCCTGGGCTGGCTGGGACCACCCTAATGCCCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:46095877..46096289;chr22:46095881..46096225 26863196 MeRIP-seq:(Medium) rs13055228 Functional Loss SNV ICGC 33..33 33 LAML 1 - 112111 RMVar_ID_112111 Human_SNP_ID_844097844 m1A Human chr22 + 29838229 29838229 29838229 GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGACCACGGTGACAGCTCCCTGAGCGCCCGCACTT GCTCTGTGCCGCCGCCGCCGCCGCCGCCGCCGTCCACGGTGACAGCTCCCTGAGCGCCCGCACTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29838118..29838250;chr22:29838106..29838275 26863196 MeRIP-seq:(Medium) rs7289250 Functional Loss SNV ICGC 33..33 33 COCA 1 - 112112 RMVar_ID_112112 Human_SNP_ID_844106586 m1A Human chr22 - 40178007 40178007 40178007 TTTTTTTGTATTTTAAATATTCAGAAACCAGCAGAGACTCTGTCGGCCATTTTGGCTTGAACTAA TTTTTTTGTATTTTAAATATTCAGAAACCAGCGGAGACTCTGTCGGCCATTTTGGCTTGAACTAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40177965..40178126 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver 112113 RMVar_ID_112113 Human_SNP_ID_844106809 m1A Human chr22 + 37018564 37018564 37018564 CGTGTCCCGGCACTCTTCTATGTCAAAGAAAGAGGCGCCGGGTACGTGGCGCTCGAGGTACTCCT CGTGTCCCGGCACTCTTCTATGTCAAAGAAAGGGGCGCCGGGTACGTGGCGCTCGAGGTACTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37018519..37018604 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver 112114 RMVar_ID_112114 Human_SNP_ID_844112576 m1A Human chr22 - 17104291 17104291 17104291 CACACCACTCTCTCCACCTGTGCACGCTCCCCACTCCAGCCACACCACACTCTCCACCTGTGCAC CACACCACTCTCTCCACCTGTGCACGCTCCCCCCTCCAGCCACACCACACTCTCCACCTGTGCAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17104249..17104318 26863196 MeRIP-seq:(Medium) rs1177346246 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 112115 RMVar_ID_112115 Human_SNP_ID_844114681 m1A Human chr22 + 35406701 35406701 35406701 CAACATTGCCATGCGCCCTGGCCTCGAGGGCTATGCCCTGCCCAGGAAGTGCAACACGTGAGTCT CAACATTGCCATGCGCCCTGGCCTCGAGGGCTGTGCCCTGCCCAGGAAGTGCAACACGTGAGTCT A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:35406651..35406750 26863196 MeRIP-seq:(Medium) rs748716384 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_245935,Human_RBP_ID_578938,Human_RBP_ID_781312,Human_RBP_ID_3963212,Human_RBP_ID_5388210,Human_RBP_ID_8865699,Human_RBP_ID_9348378,Human_RBP_ID_18194081,Human_RBP_ID_18788057,Human_RBP_ID_19009057 Human_Splice_Rec_2161647,Human_Splice_Rec_2161679,Human_Splice_Rec_2161717 Human_miRNA_ID_2041835,Human_miRNA_ID_2696378,Human_miRNA_ID_3020812 RMVar_hsa_circ_16862,RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000,RMVar_hsa_circ_112165,RMVar_hsa_circ_327159,RMVar_hsa_circ_338679,RMVar_hsa_circ_38725,RMVar_hsa_circ_11891,RMVar_hsa_circ_214001,RMVar_hsa_circ_9546,RMVar_hsa_circ_15179,RMVar_hsa_circ_214002,RMVar_hsa_circ_214003,RMVar_hsa_circ_336871,RMVar_hsa_circ_369922,RMVar_hsa_circ_90139,RMVar_hsa_circ_110329,RMVar_hsa_circ_214004,RMVar_hsa_circ_214005,RMVar_hsa_circ_267908,RMVar_hsa_circ_268345,RMVar_hsa_circ_214006 112116 RMVar_ID_112116 Human_SNP_ID_844125430 m1A Human chr22 - 39313900 39313900 39313900 AGAAGTGGGGTCTCAGGCTCAGCTGTTCAGTGATGAGGCCTGGAATGTGCGCTGGGCACAGCGCC AGAAGTGGGGTCTCAGGCTCAGCTGTTCAGTGCTGAGGCCTGGAATGTGCGCTGGGCACAGCGCC T G SNORD83B,RPL3 Ensembl:ENSG00000209480,Ensembl:ENSG00000100316 snoRNA,Protein coding exon,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39313629..39313929 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_64784,Human_RBP_ID_780833,Human_RBP_ID_833084,Human_RBP_ID_931329,Human_RBP_ID_1136864,Human_RBP_ID_1382713,Human_RBP_ID_1612041,Human_RBP_ID_1943040,Human_RBP_ID_2718998,Human_RBP_ID_3673043,Human_RBP_ID_5101851,Human_RBP_ID_5298807,Human_RBP_ID_5601716,Human_RBP_ID_7082851,Human_RBP_ID_8262362,Human_RBP_ID_8550553,Human_RBP_ID_8866271,Human_RBP_ID_9128508,Human_RBP_ID_9260802,Human_RBP_ID_9299954,Human_RBP_ID_9341365,Human_RBP_ID_9434508,Human_RBP_ID_14489464,Human_RBP_ID_17088483,Human_RBP_ID_17149042,Human_RBP_ID_17287432,Human_RBP_ID_17515270,Human_RBP_ID_17573348,Human_RBP_ID_17583821,Human_RBP_ID_17671192,Human_RBP_ID_17702370,Human_RBP_ID_17986500,Human_RBP_ID_18201462,Human_RBP_ID_18445499,Human_RBP_ID_18544761,Human_RBP_ID_18789493,Human_RBP_ID_20782783,Human_RBP_ID_22007485,Human_RBP_ID_22371887,Human_RBP_ID_22425761,Human_RBP_ID_22508384,Human_RBP_ID_22526265,Human_RBP_ID_22531690,Human_RBP_ID_22551265,Human_RBP_ID_22675897,Human_RBP_ID_22705945,Human_RBP_ID_22725550,Human_RBP_ID_22744362,Human_RBP_ID_22768493,Human_RBP_ID_23111765,Human_RBP_ID_23115780,Human_RBP_ID_23119905,Human_RBP_ID_23134434,Human_RBP_ID_23286160,Human_RBP_ID_23948226,Human_RBP_ID_24547154,Human_RBP_ID_24553887,Human_RBP_ID_24561191,Human_RBP_ID_26501321,Human_RBP_ID_26750410,Human_RBP_ID_26790067,Human_RBP_ID_27159483,Human_RBP_ID_27708526 RMVar_hsa_circ_92264,RMVar_hsa_circ_101826,RMVar_hsa_circ_214388,RMVar_hsa_circ_110607,RMVar_hsa_circ_214385,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_76609,RMVar_hsa_circ_214387,RMVar_hsa_circ_214390 112117 RMVar_ID_112117 Human_SNP_ID_844134872 m1A Human chr22 + 20145495 20145495 20145495 CTCCCCACCAACTTCTCTGCCCCAGGGACCCGAGGCCACCCCAGCCTGGTGTGGACCCATCGGCG CTCCCCACCAACTTCTCTGCCCCAGGGACCCGCGGCCACCCCAGCCTGGTGTGGACCCATCGGCG A C ZDHHC8 Ensembl:ENSG00000099904 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20145310..20146360 32194978 MeRIP-seq:(Medium) rs545639855 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_929720,Human_RBP_ID_5119878 112118 RMVar_ID_112118 Human_SNP_ID_844135966 m1A Human chr22 + 17891825 17891823 17891826 TTATGCAAATGGTATCATGACAGCGAATTCTAAGAAAAGAAACTACTAGTTTATCCAGACTCTAA TTATGCAAATGGTATCATGACAGCGAATTCT___AAAAGAAACTACTAGTTTATCCAGACTCTAA TAAG T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:17891804..17891915 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 LICA 1 - 112119 RMVar_ID_112119 Human_SNP_ID_844136984 m1A Human chr22 - 20717719 20717719 20717719 GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGAAGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG GAAGGCTTGTCTGTCGGCCCTGTCTGAAGTGACGGTGCAGCCGGGTGAGCAGGTGGCTTCTGGAG T G PI4KA Ensembl:ENSG00000241973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2845533 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_3962072,Human_RBP_ID_8865560,Human_RBP_ID_19007660 Human_Splice_Rec_2140348,Human_Splice_Rec_2140349,Human_Splice_Rec_2140372,Human_Splice_Rec_2140373,Human_Splice_Rec_2140410,Human_Splice_Rec_2140411,Human_Splice_Rec_2140438,Human_Splice_Rec_2140439,Human_Splice_Rec_2140458,Human_Splice_Rec_2140459,Human_Splice_Rec_2140485 Human_miRNA_ID_2751350 RMVar_hsa_circ_98874,RMVar_hsa_circ_123980,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213052,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_115654,RMVar_hsa_circ_213056,RMVar_hsa_circ_127180,RMVar_hsa_circ_92859,RMVar_hsa_circ_213059,RMVar_hsa_circ_213060,RMVar_hsa_circ_108566,RMVar_hsa_circ_213061,RMVar_hsa_circ_213062,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_100044,RMVar_hsa_circ_213064,RMVar_hsa_circ_213065,RMVar_hsa_circ_213067,RMVar_hsa_circ_213066,RMVar_hsa_circ_125805,RMVar_hsa_circ_83593,RMVar_hsa_circ_328224,RMVar_hsa_circ_365537 112120 RMVar_ID_112120 Human_SNP_ID_844139080 m1A Human chr22 - 17906882 17906882 17906882 TAACCACGTTTTTCTTTCTTTTTGTCAGATTAACGTGACAGTGTCAGGTGGACCCACAGCCATCC TAACCACGTTTTTCTTTCTTTTTGTCAGATTATCGTGACAGTGTCAGGTGGACCCACAGCCATCC T A MICAL3 Ensembl:ENSG00000243156 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:17906856..17906953 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_5529746,Human_RBP_ID_26344972 Human_Splice_Rec_2135010,Human_Splice_Rec_2135074,Human_Splice_Rec_2135234,Human_Splice_Rec_2135416 RMVar_hsa_circ_58884,RMVar_hsa_circ_58996,RMVar_hsa_circ_64594,RMVar_hsa_circ_212856,RMVar_hsa_circ_299244,RMVar_hsa_circ_212865,RMVar_hsa_circ_23941,RMVar_hsa_circ_300115,RMVar_hsa_circ_212867,RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_315924,RMVar_hsa_circ_212873,RMVar_hsa_circ_103449 112121 RMVar_ID_112121 Human_SNP_ID_844139383 m1A Human chr22 + 46793566 46793566 46793566 ACCAGTGAAGGCCAAGAGGGTCAGCACCTTCCAGGAGTTTGAGAGCAATACCAGCGATGCCTGGG ACCAGTGAAGGCCAAGAGGGTCAGCACCTTCCCGGAGTTTGAGAGCAATACCAGCGATGCCTGGG A C TBC1D22A Ensembl:ENSG00000054611 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46793482..46793603 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_9392515,Human_RBP_ID_18445661,Human_RBP_ID_18791777 Human_Splice_Rec_2176802,Human_Splice_Rec_2176826,Human_Splice_Rec_2176852,Human_Splice_Rec_2176858,Human_Splice_Rec_2176862,Human_Splice_Rec_2176882,Human_Splice_Rec_2176904,Human_Splice_Rec_2176930,Human_Splice_Rec_2176936,Human_Splice_Rec_2176942,Human_Splice_Rec_2176966 RMVar_hsa_circ_8138,RMVar_hsa_circ_276376,RMVar_hsa_circ_81448,RMVar_hsa_circ_333121,RMVar_hsa_circ_215148,RMVar_hsa_circ_331055,RMVar_hsa_circ_91807,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449,RMVar_hsa_circ_215149,RMVar_hsa_circ_215150,RMVar_hsa_circ_215151,RMVar_hsa_circ_335051 112122 RMVar_ID_112122 Human_SNP_ID_844148478 m1A Human chr22 + 40370687 40370687 40370687 ACCCGGATTGGCGCTGAGGTGGCCCGTGGGGCAGGTGAGTGCGGGGCGGGAGTCAGCGGAGACCC ACCCGGATTGGCGCTGAGGTGGCCCGTGGGGCGGGTGAGTGCGGGGCGGGAGTCAGCGGAGACCC A G AL022238.4,ADSL,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000239900,Ensembl:ENSG00000100359 Protein coding,Protein coding,Protein coding intron,intron,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40370601..40370847 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_3962428,Human_RBP_ID_4708670,Human_RBP_ID_18423757,Human_RBP_ID_26789839 Human_Splice_Rec_2169369,Human_Splice_Rec_2169383,Human_Splice_Rec_2169425 RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422 112123 RMVar_ID_112123 Human_SNP_ID_844152348 m1A Human chr22 - 39316948 39316948 39316948 TTGCTGGTGGAAAAGGCTCCTTAGAAGCCGGCAATGAGCTCCATCCCCACGCGGTGCCAGTGTGC TTGCTGGTGGAAAAGGCTCCTTAGAAGCCGGCGATGAGCTCCATCCCCACGCGGTGCCAGTGTGC T C RPL3 Ensembl:ENSG00000100316 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:39316947..39317148 32194978 MeRIP-seq:(Medium) rs776958654 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4698643,Human_RBP_ID_9126721,Human_RBP_ID_9392994,Human_RBP_ID_27308362 Human_Splice_Rec_2168136,Human_Splice_Rec_2168200 Human_miRNA_ID_2726847 RMVar_hsa_circ_34133,RMVar_hsa_circ_101826,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_214387,RMVar_hsa_circ_375411,RMVar_hsa_circ_76935,RMVar_hsa_circ_13806,RMVar_hsa_circ_214392,RMVar_hsa_circ_92048,RMVar_hsa_circ_214393,RMVar_hsa_circ_86942,RMVar_hsa_circ_93986,RMVar_hsa_circ_84461,RMVar_hsa_circ_214394,RMVar_hsa_circ_214396,RMVar_hsa_circ_214397,RMVar_hsa_circ_214395 112124 RMVar_ID_112124 Human_SNP_ID_844155528 m1A Human chr22 - 29310687 29310687 29310687 GGCACGGGTCGTGCTTGTCCAGGTAATGCTCCAGCGTGTCCCAGCCACCACCCACTCGCACCATC GGCACGGGTCGTGCTTGTCCAGGTAATGCTCCGGCGTGTCCCAGCCACCACCCACTCGCACCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:29310626..29310700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 8 lung 112125 RMVar_ID_112125 Human_SNP_ID_844156032 m1A Human chr22 - 38298886 38298886 38298886 CCTCAACTTCTGCCGCTCCCTGCGGTTTGACGACAAGCCCGACTACTCTTACCTACGTCAGCTCT CCTCAACTTCTGCCGCTCCCTGCGGTTTGACGGCAAGCCCGACTACTCTTACCTACGTCAGCTCT T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38298702..38298891 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_65744,Human_RBP_ID_580075,Human_RBP_ID_1611490,Human_RBP_ID_4697145,Human_RBP_ID_8863549,Human_RBP_ID_9126442,Human_RBP_ID_17285960,Human_RBP_ID_17515146,Human_RBP_ID_17986088,Human_RBP_ID_18194122,Human_RBP_ID_18788995,Human_RBP_ID_22269954,Human_RBP_ID_22820560,Human_RBP_ID_23947224,Human_RBP_ID_27037369,Human_RBP_ID_27307909,Human_RBP_ID_27493955 Human_Splice_Rec_2166580,Human_Splice_Rec_2166600,Human_Splice_Rec_2166638,Human_Splice_Rec_2166648,Human_Splice_Rec_2166670,Human_Splice_Rec_2166684,Human_Splice_Rec_2166692,Human_Splice_Rec_2166694,Human_Splice_Rec_2166698,Human_Splice_Rec_2166708,Human_Splice_Rec_2166740 Human_miRNA_ID_2580098 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_214278,RMVar_hsa_circ_87863,RMVar_hsa_circ_330107,RMVar_hsa_circ_371289,RMVar_hsa_circ_372348,RMVar_hsa_circ_105866,RMVar_hsa_circ_302161,RMVar_hsa_circ_88160,RMVar_hsa_circ_214280,RMVar_hsa_circ_214282,RMVar_hsa_circ_214284,RMVar_hsa_circ_77501,RMVar_hsa_circ_214283,RMVar_hsa_circ_214281,RMVar_hsa_circ_214279 112126 RMVar_ID_112126 Human_SNP_ID_844158935 m1A Human chr22 - 21628458 21628458 21628458 CTCCAAGAGGCCAGGGGAGGAGGTCCCCTGTGAGCCCACTCTGGAACCCTTCCTGGAACCCTCCC CTCCAAGAGGCCAGGGGAGGAGGTCCCCTGTGCGCCCACTCTGGAACCCTTCCTGGAACCCTCCC T G YDJC Ensembl:ENSG00000161179 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - Human_RBP_ID_576069,Human_RBP_ID_9300251,Human_RBP_ID_17087912,Human_RBP_ID_17982677,Human_RBP_ID_18952827,Human_RBP_ID_23119851,Human_RBP_ID_23936776,Human_RBP_ID_27032887,Human_RBP_ID_27305045 Human_miRNA_ID_2778635,Human_miRNA_ID_2826295,Human_miRNA_ID_2860267 RMVar_hsa_circ_87313,RMVar_hsa_circ_122365,RMVar_hsa_circ_79488,RMVar_hsa_circ_85961,RMVar_hsa_circ_213155,RMVar_hsa_circ_213156,RMVar_hsa_circ_213157,RMVar_hsa_circ_213154 112127 RMVar_ID_112127 Human_SNP_ID_844163969 m1A Human chr22 + 42090728 42090728 42090728 CGAAGGTGCTGGCGGTAGAAGTAGCTTGGCGGACGCCGCTCCCCGCCATCTTGCCAAAGCATCCA CGAAGGTGCTGGCGGTAGAAGTAGCTTGGCGGCCGCCGCTCCCCGCCATCTTGCCAAAGCATCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:42090536..42090775 26863196 MeRIP-seq:(Medium) rs371574739 Functional Loss SNV ICGC 33..33 33 BLCA 1 - 112128 RMVar_ID_112128 Human_SNP_ID_844174991 m1A Human chr22 + 35299925 35299925 35299925 TGATTCCCGGGGTTGGTGGCAGCGGCGGTAGCAGCAATGGACTTTCTCCTGGGGAACCCGTTCAG TGATTCCCGGGGTTGGTGGCAGCGGCGGTAGCCGCAATGGACTTTCTCCTGGGGAACCCGTTCAG A C TOM1 Ensembl:ENSG00000100284 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:35299876..35300119 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_23119866 Human_Splice_Rec_2161383,Human_Splice_Rec_2161401,Human_Splice_Rec_2161429,Human_Splice_Rec_2161455,Human_Splice_Rec_2161487,Human_Splice_Rec_2161489,Human_Splice_Rec_2161503,Human_Splice_Rec_2161507,Human_Splice_Rec_2161519,Human_Splice_Rec_2161545,Human_Splice_Rec_2161555,Human_Splice_Rec_2161563 112129 RMVar_ID_112129 Human_SNP_ID_844175028 m1A Human chr22 - 40856631 40856631 40856631 CGGGGAGGTTCTAGTCTGTTCTGTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCA CGGGGAGGTTCTAGTCTGTTCTGTCTTGCGGCGGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCA T C ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1209211684 Functional Loss SNV TCGA 33..33 33 SKCM 1 - Human_RBP_ID_4699849,Human_RBP_ID_22454482 112130 RMVar_ID_112130 Human_SNP_ID_844178141 m1A Human chr22 - 19036865 19036865 19036865 GGACTGGGACGCTTCCTTTGGGGACCAGAGGAACATTAGGGGCCGGTCAGACACGTAGGGGGCAG GGACTGGGACGCTTCCTTTGGGGACCAGAGGAGCATTAGGGGCCGGTCAGACACGTAGGGGGCAG T C DGCR2 Ensembl:ENSG00000070413 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:19036814..19036977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 4 haematopoietic and lymphoid tissue Human_RBP_ID_575099,Human_RBP_ID_1068856,Human_RBP_ID_7061072,Human_RBP_ID_14388961,Human_RBP_ID_27491480 112131 RMVar_ID_112131 Human_SNP_ID_844179614 m1A Human chr22 - 24557758 24557758 24557758 ATGTTGTCCTCTGCTTCAATGAGCTTCCCCCGATATACCTCACCGGTGTTCGTCTCACATGTCAC ATGTTGTCCTCTGCTTCAATGAGCTTCCCCCGGTATACCTCACCGGTGTTCGTCTCACATGTCAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:24557709..24557854 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 112132 RMVar_ID_112132 Human_SNP_ID_844181067 m1A Human chr22 - 29299711 29299711 29299711 CCTCGGTCCATGCCCCGGCCACCACGGAAGCCACCTCTGTCTCCACCACGGCCACCTCTGAACAT CCTCGGTCCATGCCCCGGCCACCACGGAAGCCGCCTCTGTCTCCACCACGGCCACCTCTGAACAT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:29299576..29299875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 9 brain 112133 RMVar_ID_112133 Human_SNP_ID_844189880 m1A Human chr22 - 38294442 38294442 38294442 AGGATGGGGCAGCTACGGGGGTCCGCGACCCGAGCCCTGCCCCCTGGCCCACCCACGGGGGCCAC AGGATGGGGCAGCTACGGGGGTCCGCGACCCGTGCCCTGCCCCCTGGCCCACCCACGGGGGCCAC T A TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:38294394..38294483 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_580036,Human_RBP_ID_929452 Human_Splice_Rec_2166582,Human_Splice_Rec_2166602,Human_Splice_Rec_2166616,Human_Splice_Rec_2166640,Human_Splice_Rec_2166652,Human_Splice_Rec_2166742 Human_miRNA_ID_2663929,Human_miRNA_ID_2682388,Human_miRNA_ID_2982393 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_378565,RMVar_hsa_circ_58767,RMVar_hsa_circ_214277 112134 RMVar_ID_112134 Human_SNP_ID_844190132 m1A Human chr22 + 37954768 37954752 37954769 GTGGGTGCAAAGAGAGCTAGTCTGAAGATAAAAATAAGAAACGTGTGGGATTGCTACCCCATTCC GTGGGTGCAAAGAGAGC_________________TAAGAAACGTGTGGGATTGCTACCCCATTCC CTAGTCTGAAGATAAAAA C POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:37954766..37955020 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 18..34 33 LICA 1 - 112135 RMVar_ID_112135 Human_SNP_ID_844192539 m1A Human chr22 + 35424376 35424376 35424376 CCTCCCCACTGCAGCCCTCGAACTTCCCAGGCACCCTCCTTTCTGCCCCAGAGGAAGGAGCTGTA CCTCCCCACTGCAGCCCTCGAACTTCCCAGGCCCCCTCCTTTCTGCCCCAGAGGAAGGAGCTGTA A C MCM5 Ensembl:ENSG00000100297 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:35424326..35424400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_578946,Human_RBP_ID_833936,Human_RBP_ID_5119727,Human_RBP_ID_5149004,Human_RBP_ID_9392233,Human_RBP_ID_14466521,Human_RBP_ID_17515821,Human_RBP_ID_17660275,Human_RBP_ID_17985374,Human_RBP_ID_27036221,Human_RBP_ID_27307229,Human_RBP_ID_27493467 Human_miRNA_ID_2435577 RMVar_hsa_circ_113387,RMVar_hsa_circ_214011,RMVar_hsa_circ_103796,RMVar_hsa_circ_111102,RMVar_hsa_circ_127853,RMVar_hsa_circ_214015,RMVar_hsa_circ_214014,RMVar_hsa_circ_214018 112136 RMVar_ID_112136 Human_SNP_ID_844194255 m1A Human chr22 - 38299946 38299946 38299946 CAGCCACCAAGCGCCAGAAGTATGAACGGATCAGCGAGAAGAAGATGTCAACGCCCATCGAGGTC CAGCCACCAAGCGCCAGAAGTATGAACGGATCTGCGAGAAGAAGATGTCAACGCCCATCGAGGTC T A TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38299868..38300001 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_65745,Human_RBP_ID_580078,Human_RBP_ID_1029338,Human_RBP_ID_1611492,Human_RBP_ID_1942725,Human_RBP_ID_5599428,Human_RBP_ID_7081170,Human_RBP_ID_8262341,Human_RBP_ID_9392961,Human_RBP_ID_14484085,Human_RBP_ID_17515150,Human_RBP_ID_18445455,Human_RBP_ID_18535190,Human_RBP_ID_19009204,Human_RBP_ID_23947227 Human_Splice_Rec_2166579,Human_Splice_Rec_2166599,Human_Splice_Rec_2166637,Human_Splice_Rec_2166647,Human_Splice_Rec_2166669,Human_Splice_Rec_2166683,Human_Splice_Rec_2166691,Human_Splice_Rec_2166693,Human_Splice_Rec_2166697,Human_Splice_Rec_2166707,Human_Splice_Rec_2166739 Human_miRNA_ID_2722883 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_214278,RMVar_hsa_circ_330107,RMVar_hsa_circ_371289,RMVar_hsa_circ_372348,RMVar_hsa_circ_105866,RMVar_hsa_circ_302161,RMVar_hsa_circ_88160,RMVar_hsa_circ_214280,RMVar_hsa_circ_214282,RMVar_hsa_circ_77501,RMVar_hsa_circ_214283,RMVar_hsa_circ_214281,RMVar_hsa_circ_214279,RMVar_hsa_circ_26623,RMVar_hsa_circ_294250,RMVar_hsa_circ_374717,RMVar_hsa_circ_125726,RMVar_hsa_circ_214286,RMVar_hsa_circ_214287,RMVar_hsa_circ_214285 112137 RMVar_ID_112137 Human_SNP_ID_844196934 m1A Human chr22 + 37805989 37805989 37805989 CCAAAGCCACCCCGGTCAAGAAGGCCAAGAAGAAGCTGGCTGCCACGCCCAAGAAAGCCAAAAAA CCAAAGCCACCCCGGTCAAGAAGGCCAAGAAGCAGCTGGCTGCCACGCCCAAGAAAGCCAAAAAA A C H1-0 Ensembl:ENSG00000189060 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1207094993 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_9392351,Human_RBP_ID_24547090 RMVar_hsa_circ_214211 112138 RMVar_ID_112138 Human_SNP_ID_844204750 m1A Human chr22 - 42628283 42628283 42628283 GCTGGGGACTGAGGGCTGCGGGGGTGTCTTGCAGGTTTACTTCAAGGACACCCATCCCAAGTTTC GCTGGGGACTGAGGGCTGCGGGGGTGTCTTGCTGGTTTACTTCAAGGACACCCATCCCAAGTTTC T A CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:42628251..42628425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney Human_RBP_ID_19113618,Human_RBP_ID_22455055,Human_RBP_ID_22675787 RMVar_hsa_circ_68033,RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591 112139 RMVar_ID_112139 Human_SNP_ID_844214606 m1A Human chr22 + 31399669 31399669 31399669 GGGTGTGTGAAGGGAGACAGTGTGGAGGCCACAGGGTACTCGCCACGATGAGCAGCACCTTAGCT GGGTGTGTGAAGGGAGACAGTGTGGAGGCCACCGGGTACTCGCCACGATGAGCAGCACCTTAGCT A C DRG1 Ensembl:ENSG00000185721 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:31399601..31399762 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUSC 1 - Human_RBP_ID_781703,Human_RBP_ID_1610302,Human_RBP_ID_4693152,Human_RBP_ID_5324165,Human_RBP_ID_9348372,Human_RBP_ID_22455202,Human_RBP_ID_23212732,Human_RBP_ID_27841112 Human_Splice_Rec_2155761,Human_Splice_Rec_2155777,Human_Splice_Rec_2155787,Human_Splice_Rec_2155799 RMVar_hsa_circ_113269,RMVar_hsa_circ_122524,RMVar_hsa_circ_213801,RMVar_hsa_circ_213802 112140 RMVar_ID_112140 Human_SNP_ID_844217518 m1A Human chr22 + 36288830 36288830 36288830 CCTTCATGGCCTGCAGGTTGACCTCCAACCGCAGCTTGGCATCTTCGGTGGCCTGCAGCTCGTCC CCTTCATGGCCTGCAGGTTGACCTCCAACCGCGGCTTGGCATCTTCGGTGGCCTGCAGCTCGTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36288726..36288875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 112141 RMVar_ID_112141 Human_SNP_ID_844219472 m1A Human chr22 - 42596233 42596233 42596233 TTCGAACAAAAGCCTTGACCAACATGTCCCGGACACTGGTGAACAAGGAAGAACCCCCCAAAGAG TTCGAACAAAAGCCTTGACCAACATGTCCCGGGCACTGGTGAACAAGGAAGAACCCCCCAAAGAG T C POLDIP3 Ensembl:ENSG00000100227 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:42596140..42596314;chr22:42596133..42596302 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cerebellum astrocytoma_Grade_IV,central_nervous_system astrocytoma_Grade_IV 5 brain Human_RBP_ID_14514761,Human_RBP_ID_17399562,Human_RBP_ID_18790975 Human_Splice_Rec_2172739,Human_Splice_Rec_2172755,Human_Splice_Rec_2172769,Human_Splice_Rec_2172791,Human_Splice_Rec_2172811 Human_miRNA_ID_2176152,Human_miRNA_ID_2179597 RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_214797,RMVar_hsa_circ_290888,RMVar_hsa_circ_285350,RMVar_hsa_circ_352328,RMVar_hsa_circ_359823,RMVar_hsa_circ_314204,RMVar_hsa_circ_214801,RMVar_hsa_circ_39802,RMVar_hsa_circ_214800 112142 RMVar_ID_112142 Human_SNP_ID_844239507 m1A Human chr22 + 43989161 43989161 43989161 AAGCGTACTGGGCCGGCGGCCTGCACCTCTACACCCCATTACCTTTCCGGCCAGGCCAGGGTGGC AAGCGTACTGGGCCGGCGGCCTGCACCTCTACTCCCCATTACCTTTCCGGCCAGGCCAGGGTGGC A T SAMM50 Ensembl:ENSG00000100347 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:43989080..43989181 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_245997,Human_RBP_ID_17399587,Human_RBP_ID_17988067,Human_RBP_ID_18209646,Human_RBP_ID_22454516,Human_RBP_ID_27495159 Human_Splice_Rec_2173930,Human_Splice_Rec_2173931,Human_Splice_Rec_2173944,Human_Splice_Rec_2173945,Human_Splice_Rec_2173949 RMVar_hsa_circ_116390,RMVar_hsa_circ_23770,RMVar_hsa_circ_124038,RMVar_hsa_circ_352132,RMVar_hsa_circ_76226,RMVar_hsa_circ_214929,RMVar_hsa_circ_214930,RMVar_hsa_circ_19549,RMVar_hsa_circ_214932,RMVar_hsa_circ_320114 112143 RMVar_ID_112143 Human_SNP_ID_844240390 m1A Human chr22 + 26677895 26677895 26677895 AACCTTGAAGGATGGGGAATAGTCAATAAATCAGGAGAAAATAGTGATGGTGCAGGGCATTTCAG AACCTTGAAGGATGGGGAATAGTCAATAAATCCGGAGAAAATAGTGATGGTGCAGGGCATTTCAG A C MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:26677860..26678107 26863196 MeRIP-seq:(Medium) rs739312 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_11659,GWAS_ID_11660,GWAS_ID_11661 112144 RMVar_ID_112144 Human_SNP_ID_844241336 m1A Human chr22 + 37922052 37922052 37922052 GCCTGAGGAGGGCACCTTTGTGTGTGCAGAACACTGTGCCAGGCTGGGCCCGGGGACACGGTCGG GCCTGAGGAGGGCACCTTTGTGTGTGCAGAACTCTGTGCCAGGCTGGGCCCGGGGACACGGTCGG A T MICALL1 Ensembl:ENSG00000100139 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37922001..37922102 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_4696607,Human_RBP_ID_8863496,Human_RBP_ID_14480448 Human_Splice_Rec_2165322,Human_Splice_Rec_2165332,Human_Splice_Rec_2165358 RMVar_hsa_circ_99330,RMVar_hsa_circ_30695,RMVar_hsa_circ_120352,RMVar_hsa_circ_343954,RMVar_hsa_circ_35902,RMVar_hsa_circ_124624,RMVar_hsa_circ_214248,RMVar_hsa_circ_115279,RMVar_hsa_circ_214250,RMVar_hsa_circ_214252,RMVar_hsa_circ_91660,RMVar_hsa_circ_214253,RMVar_hsa_circ_214251,RMVar_hsa_circ_38834,RMVar_hsa_circ_333064 112145 RMVar_ID_112145 Human_SNP_ID_844242461 m1A Human chr22 - 39317576 39317576 39317576 TGGAGGCTGTGACCATTGTAGAGACACCACCCATGGTGGTTGTGGGCATTGTGGGCTACGTGGAA TGGAGGCTGTGACCATTGTAGAGACACCACCCGTGGTGGTTGTGGGCATTGTGGGCTACGTGGAA T C RPL3 Ensembl:ENSG00000100316 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr22:39317478..39317675;chr22:39317526..39317600 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_580729,Human_RBP_ID_1029421,Human_RBP_ID_1136643,Human_RBP_ID_1612075,Human_RBP_ID_1943055,Human_RBP_ID_4712796,Human_RBP_ID_5203037,Human_RBP_ID_5599465,Human_RBP_ID_7082866,Human_RBP_ID_8550585,Human_RBP_ID_8863716,Human_RBP_ID_14489597,Human_RBP_ID_17286070,Human_RBP_ID_17986508,Human_RBP_ID_18194128,Human_RBP_ID_18329424,Human_RBP_ID_18789528,Human_RBP_ID_22508088,Human_RBP_ID_22820981,Human_RBP_ID_23013668,Human_RBP_ID_23212949,Human_RBP_ID_26498631,Human_RBP_ID_26823242,Human_RBP_ID_27038128,Human_RBP_ID_27308368 Human_Splice_Rec_2168094,Human_Splice_Rec_2168112,Human_Splice_Rec_2168134,Human_Splice_Rec_2168156,Human_Splice_Rec_2168178,Human_Splice_Rec_2168190,Human_Splice_Rec_2168198,Human_Splice_Rec_2168206,Human_Splice_Rec_2168210 Human_miRNA_ID_2496851,Human_miRNA_ID_2498077 RMVar_hsa_circ_101826,RMVar_hsa_circ_214386,RMVar_hsa_circ_80619,RMVar_hsa_circ_214387,RMVar_hsa_circ_375411,RMVar_hsa_circ_76935,RMVar_hsa_circ_13806,RMVar_hsa_circ_214392,RMVar_hsa_circ_86942,RMVar_hsa_circ_84461,RMVar_hsa_circ_214396,RMVar_hsa_circ_214397,RMVar_hsa_circ_214395,RMVar_hsa_circ_214398,RMVar_hsa_circ_79010 112146 RMVar_ID_112146 Human_SNP_ID_844244797 m1A Human chr22 + 17103851 17103851 17103851 GGTGGAGAGAGTGGTGTGGACGGGAGTGGGGAACGTGCACAGGTGGAGAGAGTGGTGTGGCTGGG GGTGGAGAGAGTGGTGTGGACGGGAGTGGGGAGCGTGCACAGGTGGAGAGAGTGGTGTGGCTGGG A G IL17RA Ensembl:ENSG00000177663 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:17103561..17103933 26863196 MeRIP-seq:(Medium) rs112065328 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,prostate adenocarcinoma,LUSC,skin mycosis_fungoides-Sezary_syndrome 5 skin,prostate,haematopoietic and lymphoid tissue Human_RBP_ID_8207090,Human_RBP_ID_22604029 RMVar_hsa_circ_30915,RMVar_hsa_circ_112989,RMVar_hsa_circ_212814,RMVar_hsa_circ_212815,RMVar_hsa_circ_80702,RMVar_hsa_circ_87282,RMVar_hsa_circ_91856,RMVar_hsa_circ_212816,RMVar_hsa_circ_212817 112147 RMVar_ID_112147 Human_SNP_ID_844248238 m1A Human chr22 - 36349225 36349225 36349225 AGGTCCTGGCTATAAGTCACCATGGCACAGCAAGCTGCCGATAAGTATCTCTATGTGGATAAAAA AGGTCCTGGCTATAAGTCACCATGGCACAGCAGGCTGCCGATAAGTATCTCTATGTGGATAAAAA T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:36349201..36349225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_579201,Human_RBP_ID_4708976,Human_RBP_ID_5530110,Human_RBP_ID_26822457 Human_Splice_Rec_2162448,Human_Splice_Rec_2162568,Human_Splice_Rec_2162580 RMVar_hsa_circ_20035,RMVar_hsa_circ_114176,RMVar_hsa_circ_109468,RMVar_hsa_circ_214087,RMVar_hsa_circ_305947,RMVar_hsa_circ_116297,RMVar_hsa_circ_102348,RMVar_hsa_circ_214102,RMVar_hsa_circ_214103,RMVar_hsa_circ_281298,RMVar_hsa_circ_214104,RMVar_hsa_circ_214105,RMVar_hsa_circ_214107,RMVar_hsa_circ_305266 112148 RMVar_ID_112148 Human_SNP_ID_844250772 m1A Human chr22 - 38247832 38247832 38247832 CTGCCATGGAGCAGCCTGTGTTCCTGATGACAACTGCCGCTCAGGCCATCTCTGGCTTCTTCGTG CTGCCATGGAGCAGCCTGTGTTCCTGATGACAGCTGCCGCTCAGGCCATCTCTGGCTTCTTCGTG T C TMEM184B Ensembl:ENSG00000198792 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:38247709..38247925 26863196 MeRIP-seq:(Medium) rs763261821 Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_Splice_Rec_2166461,Human_Splice_Rec_2166477,Human_Splice_Rec_2166495,Human_Splice_Rec_2166551,Human_Splice_Rec_2166557,Human_Splice_Rec_2166565 RMVar_hsa_circ_41314,RMVar_hsa_circ_318579,RMVar_hsa_circ_214271,RMVar_hsa_circ_214272,RMVar_hsa_circ_341070,RMVar_hsa_circ_280465,RMVar_hsa_circ_214274,RMVar_hsa_circ_214275,RMVar_hsa_circ_319660 112149 RMVar_ID_112149 Human_SNP_ID_844252938 m1A Human chr22 - 35393561 35393561 35393561 TGGCATAAAGCCCTACAGCAACTGTCGCCACCAGAAAGCTGAGTGTAAGGACCCATCGGAGAAGC TGGCATAAAGCCCTACAGCAACTGTCGCCACCTGAAAGCTGAGTGTAAGGACCCATCGGAGAAGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:35393512..35393595 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 112150 RMVar_ID_112150 Human_SNP_ID_844260537 m1A Human chr22 - 41339928 41339928 41339928 AGGAGGCGGGGGGCAGTGGGCTGGAGACAGGGATGGAGCCACCCACCACAGGTGGTAGCAGTGGG AGGAGGCGGGGGGCAGTGGGCTGGAGACAGGGGTGGAGCCACCCACCACAGGTGGTAGCAGTGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41339878..41340071 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain RMVar_hsa_circ_214651 112151 RMVar_ID_112151 Human_SNP_ID_844263632 m1A Human chr22 - 47137712 47137712 47137712 CCCACTTGCGCCCACCCTTCTTCCCCAGTGGTAAGCAGCCATGAAGATACCGCCTGCTTCAGGGG CCCACTTGCGCCCACCCTTCTTCCCCAGTGGTGAGCAGCCATGAAGATACCGCCTGCTTCAGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:47137709..47137819 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 112152 RMVar_ID_112152 Human_SNP_ID_844264683 m1A Human chr22 - 22303299 22303299 22303299 TGACCAAGAACAGCCAGCTACGACAAAGTCATACCTGAGTATCGGGGCCCGATTTTCCCTTGTGC TGACCAAGAACAGCCAGCTACGACAAAGTCATGCCTGAGTATCGGGGCCCGATTTTCCCTTGTGC T C lnc-ZNF280B-6 RNACentral:URS0000D5AEA8 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22303226..22303300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 112153 RMVar_ID_112153 Human_SNP_ID_844271908 m1A Human chr22 - 28742130 28742130 28742130 TTCTGGGAACCCCTGTCGGCCAAAACCCCCACACCCGGAGCAAAGCCCCGGCTCTCCCCCGCCAC TTCTGGGAACCCCTGTCGGCCAAAACCCCCACCCCCGGAGCAAAGCCCCGGCTCTCCCCCGCCAC T G CHEK2 Ensembl:ENSG00000183765 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:28742079..28742238 26863196 MeRIP-seq:(Medium) rs751442241 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary 112154 RMVar_ID_112154 Human_SNP_ID_844279948 m1A Human chr22 + 30386713 30386713 30386713 CCGCCTGCTCCTTGCCCACGTATGCCACTGCAATCCAGCCTTCCACTGGTGCCTCCTGCTCGGCA CCGCCTGCTCCTTGCCCACGTATGCCACTGCAGTCCAGCCTTCCACTGGTGCCTCCTGCTCGGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30386595..30386790 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 112155 RMVar_ID_112155 Human_SNP_ID_844283069 m1A Human chr22 - 46587852 46587848 46587852 CGGCCCCACCCCGACGCCCGGGCTTCTGGCGCACACGCCTGTTTCACTTCCTCTCCACCAAACAT CGGCCCCACCCCGACGCCCGGGCTTCTGGCGC____GCCTGTTTCACTTCCTCTCCACCAAACAT CGTGT C lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:46587841..46587962 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..36 33 ESCA 1 - 112156 RMVar_ID_112156 Human_SNP_ID_844286022 m1A Human chr22 - 42649342 42649342 42649342 GCGCGACGGTCTCGGCGGCGGCGGCGGCGGCGACAGAGCGAGCGCGGCGCGGGGCCACCATGGGG GCGCGACGGTCTCGGCGGCGGCGGCGGCGGCGGCAGAGCGAGCGCGGCGCGGGGCCACCATGGGG T C CYB5R3 Ensembl:ENSG00000100243 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:42649238..42649375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_781844,Human_RBP_ID_4708292,Human_RBP_ID_18471507 Human_Splice_Rec_2172845 112157 RMVar_ID_112157 Human_SNP_ID_844293817 m1A Human chr22 + 41586169 41586169 41586169 GATCTGCACTCTACTTCGTAGCTTCTGCAGGAAGGCGGCCACCTCAGGGTCAATTTTCTATGGGG GATCTGCACTCTACTTCGTAGCTTCTGCAGGAGGGCGGCCACCTCAGGGTCAATTTTCTATGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41586118..41586236 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 112158 RMVar_ID_112158 Human_SNP_ID_844308504 m1A Human chr22 + 17146181 17146181 17146181 GTTCTTTCCTTCCTCTCCCTATCCCATTCCCAACCTCCTACTTCCCCTGCTTAGGAGCTTAGCCA GTTCTTTCCTTCCTCTCCCTATCCCATTCCCAGCCTCCTACTTCCCCTGCTTAGGAGCTTAGCCA A G NONHSAG033192.2 RNACentral:URS00008C2B54 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17146179..17146352 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112159 RMVar_ID_112159 Human_SNP_ID_844312104 m1A Human chr22 - 30492506 30492506 30492506 GGCCTTCAACTTGGTCAAGTCGTTCATGAGTGAGGAGACACGCAGGAAGATTGTGATTCTGGGAG GGCCTTCAACTTGGTCAAGTCGTTCATGAGTGTGGAGACACGCAGGAAGATTGTGATTCTGGGAG T A SEC14L4 Ensembl:ENSG00000133488 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:30492474..30492606 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUSC 1 - Human_Splice_Rec_2153716,Human_Splice_Rec_2153717,Human_Splice_Rec_2153740,Human_Splice_Rec_2153741,Human_Splice_Rec_2153762,Human_Splice_Rec_2153763,Human_Splice_Rec_2153784,Human_Splice_Rec_2153785 112160 RMVar_ID_112160 Human_SNP_ID_844315607 m1A Human chr22 + 20566651 20566651 20566651 GCCCTCCCAGGCTCTGCCCCAGCAGCTGCAGCAGATGCATCACACACAGCACCACCAGCCGCCAC GCCCTCCCAGGCTCTGCCCCAGCAGCTGCAGCGGATGCATCACACACAGCACCACCAGCCGCCAC A G MED15 Ensembl:ENSG00000099917 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20566601..20566759 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_833462,Human_RBP_ID_17399693,Human_RBP_ID_22533803 RMVar_hsa_circ_8148,RMVar_hsa_circ_321131,RMVar_hsa_circ_265322,RMVar_hsa_circ_31298,RMVar_hsa_circ_53337,RMVar_hsa_circ_326985,RMVar_hsa_circ_313511,RMVar_hsa_circ_282443,RMVar_hsa_circ_213046,RMVar_hsa_circ_304687,RMVar_hsa_circ_213045,RMVar_hsa_circ_317420,RMVar_hsa_circ_213048,RMVar_hsa_circ_305148 112161 RMVar_ID_112161 Human_SNP_ID_844316607 m1A Human chr22 - 43179669 43179669 43179669 AGTGCATGCTGCTGCCCTGGGCCCCCACCGACATGCTGGACCTCAGCTCTTGCACACCCGAGCCG AGTGCATGCTGCTGCCCTGGGCCCCCACCGACGTGCTGGACCTCAGCTCTTGCACACCCGAGCCG T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:43179567..43180029 26863196 MeRIP-seq:(Medium) rs1403458824 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_8864735,Human_RBP_ID_18791136 Human_Splice_Rec_2173334,Human_Splice_Rec_2173335 Human_miRNA_ID_2439199,Human_miRNA_ID_2442633 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_51571,RMVar_hsa_circ_38231 112162 RMVar_ID_112162 Human_SNP_ID_844320315 m1A Human chr22 + 38300008 38300008 38300008 CTGCTTTGAGCCCCTGCCAGGGCAGGGAGCCCAGGTTGAAGTACATGAGCACGTAGCCCAGGCTC CTGCTTTGAGCCCCTGCCAGGGCAGGGAGCCCGGGTTGAAGTACATGAGCACGTAGCCCAGGCTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38298920..38300025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM,UCEC 3 - 112163 RMVar_ID_112163 Human_SNP_ID_844322620 m1A Human chr22 + 31944600 31944600 31944600 AGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCGAGCCAGTGCGCGTG AGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCGGCCTCCGGCCGGCCGGCGAGCCAGTGCGCGTG A G YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:31944552..31944684 26863196 MeRIP-seq:(Medium) rs865907627 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 4 haematopoietic and lymphoid tissue Human_RBP_ID_4693756,Human_RBP_ID_5240830,Human_RBP_ID_5324763,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639,Human_RBP_ID_23943926,Human_RBP_ID_26770975 Human_miRNA_ID_2716761,Human_miRNA_ID_3052743 112164 RMVar_ID_112164 Human_SNP_ID_844323600 m1A Human chr22 + 50280880 50280878 50280881 TCACGTCCTTGTCGCCGTCCTTGGAGGGCAGGAAGAAGACGCGGTCGGTGTAGGTCTTGTAGTCC TCACGTCCTTGTCGCCGTCCTTGGAGGGCAG___GAAGACGCGGTCGGTGTAGGTCTTGTAGTCC GGAA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50280829..50280909 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 LUSC 1 - 112165 RMVar_ID_112165 Human_SNP_ID_844324549 m1A Human chr22 + 45574606 45574606 45574606 ATGCGTGTTCGACCCCGTGCACACCATCTCCCACACCGTCATCTCGCTGCCTACCTTCCGCGAGT ATGCGTGTTCGACCCCGTGCACACCATCTCCCGCACCGTCATCTCGCTGCCTACCTTCCGCGAGT A G FBLN1 Ensembl:ENSG00000077942 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr22:45565687..45577061;chr22:45574418..45574726 26863196 MeRIP-seq:(Medium) rs760283248 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_27495412 Human_Splice_Rec_2175556,Human_Splice_Rec_2175557 Human_miRNA_ID_2066261,Human_miRNA_ID_2704105,Human_miRNA_ID_2935418 RMVar_hsa_circ_289613,RMVar_hsa_circ_107083,RMVar_hsa_circ_374852,RMVar_hsa_circ_214989,RMVar_hsa_circ_214990,RMVar_hsa_circ_16850,RMVar_hsa_circ_345430,RMVar_hsa_circ_114639,RMVar_hsa_circ_111789,RMVar_hsa_circ_215004,RMVar_hsa_circ_293012,RMVar_hsa_circ_215007,RMVar_hsa_circ_91015,RMVar_hsa_circ_215008,RMVar_hsa_circ_215006 112166 RMVar_ID_112166 Human_SNP_ID_844339398 m1A Human chr22 - 43179963 43179963 43179963 TGAGGAGAAGATGCCGGTGTGGTATATCATGGACGAGTTCGGTTCGCGGATCCAGCACGCGGACG TGAGGAGAAGATGCCGGTGTGGTATATCATGGGCGAGTTCGGTTCGCGGATCCAGCACGCGGACG T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:43179913..43183042 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_RBP_ID_4703420,Human_RBP_ID_8552252,Human_RBP_ID_8864740,Human_RBP_ID_18445619 Human_Splice_Rec_2173332 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_51571,RMVar_hsa_circ_38231,RMVar_hsa_circ_214872,RMVar_hsa_circ_84197 112167 RMVar_ID_112167 Human_SNP_ID_844345301 m1A Human chr22 + 29673480 29673477 29673481 GGTGCTGGCACTGAAGATGGCTGAGGAGTCAGAGAGGAGGTGAGGGGGCACCGGGCACCAGACTG GGTGCTGGCACTGAAGATGGCTGAGGAGTC____AGGAGGTGAGGGGGCACCGGGCACCAGACTG CAGAG C NF2 Ensembl:ENSG00000186575 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29671877..29674895 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..34 33 KIRP 1 - Human_RBP_ID_27821212 Human_Splice_Rec_2151695,Human_Splice_Rec_2151725,Human_Splice_Rec_2151757,Human_Splice_Rec_2151789,Human_Splice_Rec_2151821,Human_Splice_Rec_2151851,Human_Splice_Rec_2151881,Human_Splice_Rec_2151909,Human_Splice_Rec_2151937,Human_Splice_Rec_2151981,Human_Splice_Rec_2152013,Human_Splice_Rec_2152047,Human_Splice_Rec_2152067 RMVar_hsa_circ_28274,RMVar_hsa_circ_39428,RMVar_hsa_circ_213661,RMVar_hsa_circ_73862,RMVar_hsa_circ_71457,RMVar_hsa_circ_7241 112168 RMVar_ID_112168 Human_SNP_ID_844357939 m1A Human chr22 + 38783261 38783261 38783261 TACACACACGGGCCTTCCCTCCCACTACACACACGGGCCTTCCCTCCCACTACATACACGGGCCT TACACACACGGGCCTTCCCTCCCACTACACACGCGGGCCTTCCCTCCCACTACATACACGGGCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38783258..38783345 26863196 MeRIP-seq:(Medium) rs1369694122 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 112169 RMVar_ID_112169 Human_SNP_ID_844364334 m1A Human chr22 + 40420964 40420964 40420964 GCTGCTGCAGGATCTTGGCGTAGGATGAGTCCATGGGGGGTGCCCCCCTGTCCTGCTTCTGGTCC GCTGCTGCAGGATCTTGGCGTAGGATGAGTCCGTGGGGGGTGCCCCCCTGTCCTGCTTCTGGTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:40420919..40421047 26863196 MeRIP-seq:(Medium) rs1417849237 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma,stomach adenocarcinoma 16 stomach 112170 RMVar_ID_112170 Human_SNP_ID_844365018 m1A Human chr22 - 41694309 41694309 41694309 TTTCTATTCCCTAGTTCCTGAATGTTGGTTCTACTCTCAACTCCCATCCGGTCCTGGGTGTCCCA TTTCTATTCCCTAGTTCCTGAATGTTGGTTCTGCTCTCAACTCCCATCCGGTCCTGGGTGTCCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41694093..41694343 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 112171 RMVar_ID_112171 Human_SNP_ID_844368933 m1A Human chr22 - 37029193 37029190 37029193 GGTTCAATGCCTACAGCAGGGGAGCAGGGAGGAGGGGACAAATAGAAGGATGCTATGAATGGTAC GGTTCAATGCCTACAGCAGGGGAGCAGGGAGG___GGACAAATAGAAGGATGCTATGAATGGTAC CCCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37029190..37029314 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 COAD 1 - 112172 RMVar_ID_112172 Human_SNP_ID_844377514 m1A Human chr22 - 23767886 23767886 23767886 GCTGCCGCCGTCTCTAAGGTCGCCCGGGTCCCACCGCCGCCACCATGCCTCGGGGAAGCCGCAGC GCTGCCGCCGTCTCTAAGGTCGCCCGGGTCCCGCCGCCGCCACCATGCCTCGGGGAAGCCGCAGC T C CHCHD10 Ensembl:ENSG00000250479 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr22:23767776..23767975;chr22:23767773..23767950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_576529,Human_RBP_ID_782448,Human_RBP_ID_1608868,Human_RBP_ID_4708505,Human_RBP_ID_5324144,Human_RBP_ID_5446317,Human_RBP_ID_5472886,Human_RBP_ID_5504398,Human_RBP_ID_9332765,Human_RBP_ID_22533827,Human_RBP_ID_26822307 Human_Splice_Rec_2144147,Human_Splice_Rec_2144151,Human_Splice_Rec_2144157,Human_Splice_Rec_2144165 112173 RMVar_ID_112173 Human_SNP_ID_844385926 m1A Human chr22 - 19467924 19467924 19467924 GAGCGTCAACCTTCAAGTGGCCACCTACTCCAAATTCCAACCTCAGAGCCCTGACTTCCTGGACA GAGCGTCAACCTTCAAGTGGCCACCTACTCCACATTCCAACCTCAGAGCCCTGACTTCCTGGACA T G UFD1 Ensembl:ENSG00000070010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:19467824..19468034;chr22:19467829..19468040;chr22:19467824..19468039 26863196 MeRIP-seq:(Medium) rs771636950 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1028360,Human_RBP_ID_3961954,Human_RBP_ID_5504283,Human_RBP_ID_8116784,Human_RBP_ID_9299635,Human_RBP_ID_9391940,Human_RBP_ID_14394218,Human_RBP_ID_17285019,Human_RBP_ID_17398340,Human_RBP_ID_17982204,Human_RBP_ID_19007601,Human_RBP_ID_26822185 Human_Splice_Rec_2137084,Human_Splice_Rec_2137085,Human_Splice_Rec_2137106,Human_Splice_Rec_2137107,Human_Splice_Rec_2137126,Human_Splice_Rec_2137127,Human_Splice_Rec_2137156,Human_Splice_Rec_2137157,Human_Splice_Rec_2137172,Human_Splice_Rec_2137173,Human_Splice_Rec_2137186,Human_Splice_Rec_2137187,Human_Splice_Rec_2137196,Human_Splice_Rec_2137204,Human_Splice_Rec_2137208 Human_miRNA_ID_2354566,Human_miRNA_ID_3070368 RMVar_hsa_circ_7550,RMVar_hsa_circ_212956,RMVar_hsa_circ_336707,RMVar_hsa_circ_64752,RMVar_hsa_circ_307987,RMVar_hsa_circ_372083 112174 RMVar_ID_112174 Human_SNP_ID_844385929 m1A Human chr22 - 19467924 19467924 19467924 GAGCGTCAACCTTCAAGTGGCCACCTACTCCAAATTCCAACCTCAGAGCCCTGACTTCCTGGACA GAGCGTCAACCTTCAAGTGGCCACCTACTCCAGATTCCAACCTCAGAGCCCTGACTTCCTGGACA T C UFD1 Ensembl:ENSG00000070010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:19467824..19468034;chr22:19467829..19468040;chr22:19467824..19468039 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 4 lung Human_RBP_ID_1028360,Human_RBP_ID_3961954,Human_RBP_ID_5504283,Human_RBP_ID_8116784,Human_RBP_ID_9299635,Human_RBP_ID_9391940,Human_RBP_ID_14394218,Human_RBP_ID_17285019,Human_RBP_ID_17398340,Human_RBP_ID_17982204,Human_RBP_ID_19007601,Human_RBP_ID_26822185 Human_Splice_Rec_2137084,Human_Splice_Rec_2137085,Human_Splice_Rec_2137106,Human_Splice_Rec_2137107,Human_Splice_Rec_2137126,Human_Splice_Rec_2137127,Human_Splice_Rec_2137156,Human_Splice_Rec_2137157,Human_Splice_Rec_2137172,Human_Splice_Rec_2137173,Human_Splice_Rec_2137186,Human_Splice_Rec_2137187,Human_Splice_Rec_2137196,Human_Splice_Rec_2137204,Human_Splice_Rec_2137208 Human_miRNA_ID_2354566,Human_miRNA_ID_3070368 RMVar_hsa_circ_7550,RMVar_hsa_circ_212956,RMVar_hsa_circ_336707,RMVar_hsa_circ_64752,RMVar_hsa_circ_307987,RMVar_hsa_circ_372083 112175 RMVar_ID_112175 Human_SNP_ID_844389172 m1A Human chr22 - 39522326 39522326 39522326 GCTGCTACCATCTTCTCTCCAGGAGGATCGTAAGGTTTGGGACGGGCAGACCCACAGAGAACACC GCTGCTACCATCTTCTCTCCAGGAGGATCGTACGGTTTGGGACGGGCAGACCCACAGAGAACACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:39522276..39522354 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 112176 RMVar_ID_112176 Human_SNP_ID_844394212 m1A Human chr22 + 35257821 35257821 35257821 AACGGGGAAGGCGGGAAAGCTGCGGGGCCGGGAGGGGGCGTGCGGCCGCCCCGGGGGCCTGCGGA AACGGGGAAGGCGGGAAAGCTGCGGGGCCGGGGGGGGGCGTGCGGCCGCCCCGGGGGCCTGCGGA A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:35257813..35257980;chr22:35257815..35257978 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_246588,Human_RBP_ID_5388196,Human_RBP_ID_8207315,Human_RBP_ID_9434163,Human_RBP_ID_18464182,Human_RBP_ID_22362487 112177 RMVar_ID_112177 Human_SNP_ID_844395029 m1A Human chr22 + 32039773 32039773 32039773 GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATCATTGAAGTAGATCCTGACACTAAGGAAATGCT A C Z74021.1 Ensembl:ENSG00000232346 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5275956,Human_RBP_ID_26501422 112178 RMVar_ID_112178 Human_SNP_ID_844395041 m1A Human chr22 + 32039773 32039773 32039773 GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATAATTGAAGTAGATCCTGACACTAAGGAAATGCT GTTCCTGAGGTCTCAGCCTTGGATCAGGAGATTATTGAAGTAGATCCTGACACTAAGGAAATGCT A T Z74021.1 Ensembl:ENSG00000232346 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs373723834 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5275956,Human_RBP_ID_26501422 112179 RMVar_ID_112179 Human_SNP_ID_844404651 m1A Human chr22 - 38486029 38486028 38486030 GCCACAGCCACTGATGTCACAACAGTTTGCACAGCCTCCGGGAGCTACCAATATGATAGGTTACA GCCACAGCCACTGATGTCACAACAGTTTGCA__GCCTCCGGGAGCTACCAATATGATAGGTTACA CTG C DDX17 Ensembl:ENSG00000100201 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:38485788..38486325 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 LICA 1 - Human_RBP_ID_245815,Human_RBP_ID_580230,Human_RBP_ID_1611600,Human_RBP_ID_1942804,Human_RBP_ID_3672800,Human_RBP_ID_7081605,Human_RBP_ID_9126526,Human_RBP_ID_14485568,Human_RBP_ID_18789106,Human_RBP_ID_20762188,Human_RBP_ID_23013243,Human_RBP_ID_23947497,Human_RBP_ID_24494161,Human_RBP_ID_25670089,Human_RBP_ID_27037598,Human_RBP_ID_27308007 Human_miRNA_ID_2181680,Human_miRNA_ID_2183784,Human_miRNA_ID_2716786,Human_miRNA_ID_3052768 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_101987,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_214294 112180 RMVar_ID_112180 Human_SNP_ID_844410628 m1A Human chr22 + 26483982 26483982 26483982 GCGCTCCGCGGCTCGACGGCCGCGGCGGAGGGAGGCGGCGCCCCGGGGGAGAGAGGCGGCGCCCC GCGCTCCGCGGCTCGACGGCCGCGGCGGAGGGGGGCGGCGCCCCGGGGGAGAGAGGCGGCGCCCC A G SRRD Ensembl:ENSG00000100104 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:26483901..26488016 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4708910 112181 RMVar_ID_112181 Human_SNP_ID_844412006 m1A Human chr22 + 41873901 41873901 41873901 TAAGCAGGTACCTGGGGGAGTCAAGCAGCTTGAGCCCCCCAAAGAAGGAGAAAGGCGGACAACCC TAAGCAGGTACCTGGGGGAGTCAAGCAGCTTGGGCCCCCCAAAGAAGGAGAAAGGCGGACAACCC A G SREBF2 Ensembl:ENSG00000198911 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41873856..41873962 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain Human_RBP_ID_5599501 RMVar_hsa_circ_9595,RMVar_hsa_circ_24121,RMVar_hsa_circ_122139,RMVar_hsa_circ_39627,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729,RMVar_hsa_circ_29319,RMVar_hsa_circ_8651,RMVar_hsa_circ_34127,RMVar_hsa_circ_354754,RMVar_hsa_circ_355447,RMVar_hsa_circ_37548,RMVar_hsa_circ_214734,RMVar_hsa_circ_293282,RMVar_hsa_circ_214733,RMVar_hsa_circ_125188,RMVar_hsa_circ_335945,RMVar_hsa_circ_348704,RMVar_hsa_circ_354402,RMVar_hsa_circ_334403,RMVar_hsa_circ_31482,RMVar_hsa_circ_45165,RMVar_hsa_circ_214736,RMVar_hsa_circ_214737,RMVar_hsa_circ_214735 112182 RMVar_ID_112182 Human_SNP_ID_844414518 m1A Human chr22 - 36291997 36291994 36291997 AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAGAAGTTTGACCAGGTGTGTGGCCGTTGGCCCCAT AGAGCGCGTGCAACCTGGAGAAGAAGCAGAAG___TTTGACCAGGTGTGTGGCCGTTGGCCCCAT ACTT A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36291976..36292000 26863196 MeRIP-seq:(Medium) rs889313598 Functional Loss DEL TCGA 33..35 33 CESC 1 - Human_RBP_ID_5599391,Human_RBP_ID_22087347 Human_Splice_Rec_2162507 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_90265,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_112684,RMVar_hsa_circ_214064,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_376591,RMVar_hsa_circ_214068,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072 112183 RMVar_ID_112183 Human_SNP_ID_844425193 m1A Human chr22 + 29308593 29308593 29308593 GCTGGCCCCACGCCTCGTGCAGTTTGAGCAGGAGATTGAGCGGGAGCTGCGTGCTGCACCCCCAG GCTGGCCCCACGCCTCGTGCAGTTTGAGCAGGGGATTGAGCGGGAGCTGCGTGCTGCACCCCCAG A G GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:29308543..29308683 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus 112184 RMVar_ID_112184 Human_SNP_ID_844425967 m1A Human chr22 + 23881953 23881953 23881953 GATTGAGAGAGACAGAGGCAGAGAGAGAGAGAAACACACACACACACACACACACAGAGACAGAG GATTGAGAGAGACAGAGGCAGAGAGAGAGAGACACACACACACACACACACACACAGAGACAGAG A C AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:23881945..23882121 26863196 MeRIP-seq:(Medium) rs1194954241 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_23011370 112185 RMVar_ID_112185 Human_SNP_ID_844426211 m1A Human chr22 + 31083246 31083246 31083246 GGGGATCTCACCAGAAAGGAACCGACGGAGCTAGGGGCCAGCGAGATGGCGGACGAGGCCTTAGC GGGGATCTCACCAGAAAGGAACCGACGGAGCTCGGGGCCAGCGAGATGGCGGACGAGGCCTTAGC A C SMTN Ensembl:ENSG00000183963 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:31083127..31083355;chr22:31082998..31085011;chr22:31083121..31083366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 5 haematopoietic and lymphoid tissue Human_RBP_ID_4711371,Human_RBP_ID_19007886 Human_Splice_Rec_2154778,Human_Splice_Rec_2154779,Human_Splice_Rec_2154784,Human_Splice_Rec_2154785,Human_Splice_Rec_2154790,Human_Splice_Rec_2154791,Human_Splice_Rec_2154796,Human_Splice_Rec_2154797,Human_Splice_Rec_2154804,Human_Splice_Rec_2154805,Human_Splice_Rec_2154810,Human_Splice_Rec_2154811,Human_Splice_Rec_2154818,Human_Splice_Rec_2154819,Human_Splice_Rec_2154822,Human_Splice_Rec_2154823,Human_Splice_Rec_2154862,Human_Splice_Rec_2154863,Human_Splice_Rec_2154900,Human_Splice_Rec_2154901,Human_Splice_Rec_2154940,Human_Splice_Rec_2154941,Human_Splice_Rec_2154978,Human_Splice_Rec_2154979,Human_Splice_Rec_2154988,Human_Splice_Rec_2154989 112186 RMVar_ID_112186 Human_SNP_ID_844426527 m1A Human chr22 - 38291992 38291992 38291992 ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAGTAGCCAGAGACAGCTGTGTACCTCACCTGT ACAGAGCGAGACTCCATCTCAAAAAAAAAAAAGAGTAGCCAGAGACAGCTGTGTACCTCACCTGT T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1348856800 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 112187 RMVar_ID_112187 Human_SNP_ID_844434222 m1A Human chr22 + 29671901 29671901 29671901 AGGCTGAACGCACGAGGGATGAGTTGGAGAGGAGGCTGCTGCAGATGAAAGAAGAAGCAACAATG AGGCTGAACGCACGAGGGATGAGTTGGAGAGGTGGCTGCTGCAGATGAAAGAAGAAGCAACAATG A T NF2 Ensembl:ENSG00000186575 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:29671797..29674950;chr22:29671790..29673521;chr22:29671776..29673538 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 12 caecum,large intestine Human_RBP_ID_66111,Human_RBP_ID_782433,Human_RBP_ID_1941447,Human_RBP_ID_5389054,Human_RBP_ID_7073339,Human_RBP_ID_9392150,Human_RBP_ID_14448294,Human_RBP_ID_17989388,Human_RBP_ID_26345287 Human_Splice_Rec_2151692,Human_Splice_Rec_2151693,Human_Splice_Rec_2151723,Human_Splice_Rec_2151754,Human_Splice_Rec_2151755,Human_Splice_Rec_2151786,Human_Splice_Rec_2151787,Human_Splice_Rec_2151818,Human_Splice_Rec_2151819,Human_Splice_Rec_2151848,Human_Splice_Rec_2151849,Human_Splice_Rec_2151878,Human_Splice_Rec_2151879,Human_Splice_Rec_2151906,Human_Splice_Rec_2151907,Human_Splice_Rec_2151934,Human_Splice_Rec_2151935,Human_Splice_Rec_2151978,Human_Splice_Rec_2151979,Human_Splice_Rec_2152010,Human_Splice_Rec_2152011,Human_Splice_Rec_2152044,Human_Splice_Rec_2152045,Human_Splice_Rec_2152064,Human_Splice_Rec_2152065 RMVar_hsa_circ_28274,RMVar_hsa_circ_39428,RMVar_hsa_circ_213661,RMVar_hsa_circ_73862,RMVar_hsa_circ_71457,RMVar_hsa_circ_7241 112188 RMVar_ID_112188 Human_SNP_ID_844437908 m1A Human chr22 - 37648269 37648269 37648269 CTTAGGCCAGGGGCAGAACGCACCCAGCCCTGAGAATTCTCCAGCCCAGGGTTTCCAAAGAGTGT CTTAGGCCAGGGGCAGAACGCACCCAGCCCTGGGAATTCTCCAGCCCAGGGTTTCCAAAGAGTGT T C Z83844.2 Ensembl:ENSG00000233360 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37648260..37648395 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112189 RMVar_ID_112189 Human_SNP_ID_844438882 m1A Human chr22 + 23894493 23894493 23894493 GTCCTTCTGCCATCATGCCGATGTTCATCGTAAACACCAACGTGCCCCGCGCCTCCGTGCCGGAC GTCCTTCTGCCATCATGCCGATGTTCATCGTACACACCAACGTGCCCCGCGCCTCCGTGCCGGAC A C AP000350.4,MIF Ensembl:ENSG00000251357,Ensembl:ENSG00000240972 Protein coding,Protein coding intron,CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr22:23894376..23894575;chr22:23894351..23895183 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_65766,Human_RBP_ID_576612,Human_RBP_ID_1608917,Human_RBP_ID_1940438,Human_RBP_ID_3669367,Human_RBP_ID_4688745,Human_RBP_ID_5324147,Human_RBP_ID_5424301,Human_RBP_ID_5446322,Human_RBP_ID_5472894,Human_RBP_ID_5504407,Human_RBP_ID_8546766,Human_RBP_ID_9332768,Human_RBP_ID_17660213,Human_RBP_ID_17983051,Human_RBP_ID_18194061,Human_RBP_ID_18785648,Human_RBP_ID_22454852,Human_RBP_ID_22507686,Human_RBP_ID_22819819,Human_RBP_ID_23937872,Human_RBP_ID_24493702,Human_RBP_ID_26501365,Human_RBP_ID_26822313,Human_RBP_ID_27033704,Human_RBP_ID_27305503 Human_Splice_Rec_2144785,Human_Splice_Rec_2144789 Human_miRNA_ID_2250441,Human_miRNA_ID_3066507 RMVar_hsa_circ_78844,RMVar_hsa_circ_213300 112190 RMVar_ID_112190 Human_SNP_ID_844442195 m1A Human chr22 - 46351127 46351127 46351127 CCTCTCTGGGACACCGGATCCTCTCCTCCTTCAGGTCTCAGGTTCCATGTGACTTCTTTTGAGGC CCTCTCTGGGACACCGGATCCTCTCCTCCTTCGGGTCTCAGGTTCCATGTGACTTCTTTTGAGGC T C lnc-CDPF1-1 RNACentral:URS0000D58ABB lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:46351089..46351186 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112191 RMVar_ID_112191 Human_SNP_ID_844444185 m1A Human chr22 - 17917331 17917331 17917331 TGTCCGGGTAGCTGGCGGTGTTGTTTACCAAGATGCAGAACACTAGGGAAGGAACAGGCTCTGGC TGTCCGGGTAGCTGGCGGTGTTGTTTACCAAGGTGCAGAACACTAGGGAAGGAACAGGCTCTGGC T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:17917329..17917790 26863196 MeRIP-seq:(Medium) rs1040963477 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 112192 RMVar_ID_112192 Human_SNP_ID_844445658 m1A Human chr22 - 20966909 20966909 20966909 TGCCCAACAGCATATGGGGAAAGCAAGGGGTCAAGGTCCCATCAAGGTCAAGCAGCAGGGGCATC TGCCCAACAGCATATGGGGAAAGCAAGGGGTCGAGGTCCCATCAAGGTCAAGCAGCAGGGGCATC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20966901..20967012 26863196 MeRIP-seq:(Medium) rs558893698 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112193 RMVar_ID_112193 Human_SNP_ID_844456697 m1A Human chr22 + 41173674 41173674 41173674 AAAATGCTAAAAAGAAGAATAATAAGAAAACCAGCAAAAATAAGAGCAGCCTGAGTAGGGGCAAC AAAATGCTAAAAAGAAGAATAATAAGAAAACCTGCAAAAATAAGAGCAGCCTGAGTAGGGGCAAC A T EP300 Ensembl:ENSG00000100393 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:41173601..41173700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_3962451,Human_RBP_ID_18535219,Human_RBP_ID_26346042,Human_RBP_ID_27038720 Human_Splice_Rec_2170234,Human_Splice_Rec_2170292 Human_miRNA_ID_184611,Human_miRNA_ID_2005998 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_267084,RMVar_hsa_circ_265093,RMVar_hsa_circ_362344,RMVar_hsa_circ_96540,RMVar_hsa_circ_8840,RMVar_hsa_circ_116518,RMVar_hsa_circ_214579,RMVar_hsa_circ_338980,RMVar_hsa_circ_22948,RMVar_hsa_circ_275805,RMVar_hsa_circ_37531,RMVar_hsa_circ_214586,RMVar_hsa_circ_214588,RMVar_hsa_circ_214593,RMVar_hsa_circ_214592,RMVar_hsa_circ_353322,RMVar_hsa_circ_307418,RMVar_hsa_circ_214596,RMVar_hsa_circ_298011,RMVar_hsa_circ_374831,RMVar_hsa_circ_214595,RMVar_hsa_circ_314811,RMVar_hsa_circ_214597 112194 RMVar_ID_112194 Human_SNP_ID_844458033 m1A Human chr22 - 20507651 20507651 20507651 TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTATCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT TCCATGCCTGTTCCCCAGCTCCCGCCGCCCGTTTCCCGCTTGGCCGCCACCGCCGCCGCCTCAGT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20507601..20507750 26863196 MeRIP-seq:(Medium) rs897292439 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 112195 RMVar_ID_112195 Human_SNP_ID_844481326 m1A Human chr22 - 23767587 23767587 23767587 AACCCTGCTTCCTCCCACCCCCGCAGCCGCCCAGCCGCGCCCTCTGCCCACCCGCCCGCGCACCC AACCCTGCTTCCTCCCACCCCCGCAGCCGCCCCGCCGCGCCCTCTGCCCACCCGCCCGCGCACCC T G CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:23767571..23767909 32194978 MeRIP-seq:(Medium) rs179468 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 10 head and neck Human_RBP_ID_781822,Human_RBP_ID_22533826 Human_Splice_Rec_2144152,Human_Splice_Rec_2144158 Human_miRNA_ID_2274244,Human_miRNA_ID_2874402,Human_miRNA_ID_2982362 GWAS_ID_11654,GWAS_ID_11655,GWAS_ID_11656,GWAS_ID_11657,GWAS_ID_11658 RMVar_hsa_circ_106045,RMVar_hsa_circ_213286 112196 RMVar_ID_112196 Human_SNP_ID_844484253 m1A Human chr22 + 37805296 37805285 37805297 GGAGGCAGAGGCAGAGGCAGAGGCAGAGCCCGAGCCCGGTGCCGAGACCAAGCGACAGACCGGCG GGAGGCAGAGGCAGAGGCAGAG____________CCCGGTGCCGAGACCAAGCGACAGACCGGCG GGCAGAGCCCGAG G H1-0 Ensembl:ENSG00000189060 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr22:37805251..37805475;chr22:37805251..37805590;chr22:37805251..37805550 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 23..34 33 LMS 1 - Human_RBP_ID_782062,Human_RBP_ID_4708208,Human_RBP_ID_22454978 112197 RMVar_ID_112197 Human_SNP_ID_844489059 m1A Human chr22 - 36320273 36320273 36320273 CATCCCCGGGCAGCAGGACAAGGACATGTTCCAGGAGACCATGGAGGCCATGAGGATTATGGGCA CATCCCCGGGCAGCAGGACAAGGACATGTTCCTGGAGACCATGGAGGCCATGAGGATTATGGGCA T A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:36320190..36320272 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_65288,Human_RBP_ID_930275,Human_RBP_ID_1942431,Human_RBP_ID_5599406,Human_RBP_ID_7079624,Human_RBP_ID_8865736,Human_RBP_ID_17985588,Human_RBP_ID_26345389,Human_RBP_ID_26823124,Human_RBP_ID_27307327 Human_Splice_Rec_2162462,Human_Splice_Rec_2162463,Human_Splice_Rec_2162554,Human_Splice_Rec_2162566 RMVar_hsa_circ_13348,RMVar_hsa_circ_41876,RMVar_hsa_circ_20035,RMVar_hsa_circ_114176,RMVar_hsa_circ_47568,RMVar_hsa_circ_50362,RMVar_hsa_circ_80781,RMVar_hsa_circ_214087,RMVar_hsa_circ_13182,RMVar_hsa_circ_62653,RMVar_hsa_circ_214091,RMVar_hsa_circ_214089,RMVar_hsa_circ_105269,RMVar_hsa_circ_112325,RMVar_hsa_circ_88954,RMVar_hsa_circ_214094,RMVar_hsa_circ_50291,RMVar_hsa_circ_119857,RMVar_hsa_circ_122475,RMVar_hsa_circ_214095,RMVar_hsa_circ_214096,RMVar_hsa_circ_214097 112198 RMVar_ID_112198 Human_SNP_ID_844496163 m1A Human chr22 - 19977905 19977905 19977905 CCTCATACCAAGGGCTGGAGAGACGATCATGCAGGTCCCAGGAGGCTGGAACTGTGGGAGCAGCA CCTCATACCAAGGGCTGGAGAGACGATCATGCCGGTCCCAGGAGGCTGGAACTGTGGGAGCAGCA T G ARVCF Ensembl:ENSG00000099889 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19977894..19978064 26863196 MeRIP-seq:(Medium) rs1229848436 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine RMVar_hsa_circ_23532,RMVar_hsa_circ_48736,RMVar_hsa_circ_61889,RMVar_hsa_circ_100175,RMVar_hsa_circ_96183,RMVar_hsa_circ_212982,RMVar_hsa_circ_212983 112199 RMVar_ID_112199 Human_SNP_ID_844498867 m1A Human chr22 - 45548663 45548663 45548663 GCTGCACTGGAAGCTTCCAGGGATGTTGATGCAGCGGTAGGAGCAGATGTGGCCCCCGGTGGGCA GCTGCACTGGAAGCTTCCAGGGATGTTGATGCGGCGGTAGGAGCAGATGTGGCCCCCGGTGGGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:45548569..45548785 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach 112200 RMVar_ID_112200 Human_SNP_ID_844500995 m1A Human chr22 - 39522467 39522467 39522467 TCGTTCTTCTTTTCCAGCTCTTTGCACTCACCAGTAAGAGCCTCCTGCTCCGCCCTCTTCTTCTG TCGTTCTTCTTTTCCAGCTCTTTGCACTCACCGGTAAGAGCCTCCTGCTCCGCCCTCTTCTTCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:39522245..39522700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus 112201 RMVar_ID_112201 Human_SNP_ID_844502361 m1A Human chr22 + 39319195 39319195 39319195 TTCAGGAGGACTCCACAACACTCCCCTCCCCCAAGCTTCTTTACCTCCCAATGAGAACGGCGCCG TTCAGGAGGACTCCACAACACTCCCCTCCCCCGAGCTTCTTTACCTCCCAATGAGAACGGCGCCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:39319181..39319625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112202 RMVar_ID_112202 Human_SNP_ID_844504699 m1A Human chr22 + 35400497 35400497 35400497 TTTCTACAGCGACAGCTTCGGGGGCGACGCCCAGGCCGACGAGGGGCAGGCCCGCAAATCGCAGC TTTCTACAGCGACAGCTTCGGGGGCGACGCCCGGGCCGACGAGGGGCAGGCCCGCAAATCGCAGC A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:35400476..35400500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_781308,Human_RBP_ID_1029169,Human_RBP_ID_4708588,Human_RBP_ID_9332812,Human_RBP_ID_9392223,Human_RBP_ID_18194079,Human_RBP_ID_22454430 Human_Splice_Rec_2161636,Human_Splice_Rec_2161642,Human_Splice_Rec_2161672,Human_Splice_Rec_2161706 Human_miRNA_ID_2152523,Human_miRNA_ID_2420984 RMVar_hsa_circ_118101,RMVar_hsa_circ_76816,RMVar_hsa_circ_93008,RMVar_hsa_circ_213997,RMVar_hsa_circ_213998,RMVar_hsa_circ_213999,RMVar_hsa_circ_62529,RMVar_hsa_circ_107956,RMVar_hsa_circ_214000 112203 RMVar_ID_112203 Human_SNP_ID_844505662 m1A Human chr22 - 41246610 41246610 41246610 CGCCCGCCACAGTCTGCTGCAGACGCTGTACAAGGTCTAGACTCAAAGCCTCTCCCATCCCTTGG CGCCCGCCACAGTCTGCTGCAGACGCTGTACAGGGTCTAGACTCAAAGCCTCTCCCATCCCTTGG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:41246509..41246610 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_1029587,Human_RBP_ID_1943598,Human_RBP_ID_14504321,Human_RBP_ID_18445557,Human_RBP_ID_23949950 Human_Splice_Rec_2170590,Human_Splice_Rec_2170620,Human_Splice_Rec_2170648 Human_miRNA_ID_2948095 RMVar_hsa_circ_85248,RMVar_hsa_circ_109735,RMVar_hsa_circ_117905,RMVar_hsa_circ_125273,RMVar_hsa_circ_126495,RMVar_hsa_circ_123402,RMVar_hsa_circ_114151,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_89513,RMVar_hsa_circ_214608,RMVar_hsa_circ_214612,RMVar_hsa_circ_214616,RMVar_hsa_circ_82171,RMVar_hsa_circ_82382,RMVar_hsa_circ_214618,RMVar_hsa_circ_77274,RMVar_hsa_circ_214617,RMVar_hsa_circ_214614,RMVar_hsa_circ_214615,RMVar_hsa_circ_214613,RMVar_hsa_circ_214610,RMVar_hsa_circ_214611,RMVar_hsa_circ_214609,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607 112204 RMVar_ID_112204 Human_SNP_ID_844507501 m1A Human chr22 - 23686946 23686946 23686946 GAAGTTAACTTGGTGCCATTGGGCAGAGGGTGAGAGCCCAGCAAACCGGAGAGATCAGCTGCCCA GAAGTTAACTTGGTGCCATTGGGCAGAGGGTGGGAGCCCAGCAAACCGGAGAGATCAGCTGCCCA T C GUSBP11,AP000347.1 Ensembl:ENSG00000228315,Ensembl:ENSG00000272578 lincRNA,Pseudogene exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23686905..23690246 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_3678920,Human_RBP_ID_21986520,Human_RBP_ID_24381044 Human_Splice_Rec_2143852,Human_Splice_Rec_2143874,Human_Splice_Rec_2143900,Human_Splice_Rec_2143906,Human_Splice_Rec_2143908 RMVar_hsa_circ_39823,RMVar_hsa_circ_213273,RMVar_hsa_circ_93202,RMVar_hsa_circ_347237,RMVar_hsa_circ_369337,RMVar_hsa_circ_213276,RMVar_hsa_circ_278737,RMVar_hsa_circ_213275,RMVar_hsa_circ_337871,RMVar_hsa_circ_361933,RMVar_hsa_circ_43344,RMVar_hsa_circ_52570,RMVar_hsa_circ_213277 112205 RMVar_ID_112205 Human_SNP_ID_844513650 m1A Human chr22 + 42720827 42720821 42720827 ACCTCTAGCTCCAGCGGCGGCGGGCGGCGGACAGCGGGGCCCCGGCGGGCGGGCGGCGCGGCGGC ACCTCTAGCTCCAGCGGCGGCGGGCGG______GCGGGGCCCCGGCGGGCGGGCGGCGCGGCGGC GCGGACA G lnc-SERHL2-3 RNACentral:URS00008B58C2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:42720717..42720875;chr22:42720702..42720846;chr22:42720644..42720852 26863196 MeRIP-seq:(Medium) rs1290680201 Functional Loss DEL ICGC 28..33 33 LMS 1 - 112206 RMVar_ID_112206 Human_SNP_ID_844521222 m1A Human chr22 - 40856609 40856609 40856609 GTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCACGCCGAGCCAGCGCCTGGGCCTGGAACCGGGC GTCTTGCGGCAGCCGCCCCCTTCTGCGCGGTCCCGCCGAGCCAGCGCCTGGGCCTGGAACCGGGC T G ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr22:40856426..40856675;chr22:40856533..40856632 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 THCA 2 - Human_RBP_ID_4699847,Human_RBP_ID_17399856,Human_RBP_ID_22270859,Human_RBP_ID_22454482 112207 RMVar_ID_112207 Human_SNP_ID_844527217 m1A Human chr22 + 37665677 37665677 37665677 TCACGGAGAACTTCAGCATCGACCCCGCACGCACGCTTATGGTGGGTGACCGCCTGGAGACCGAC TCACGGAGAACTTCAGCATCGACCCCGCACGCGCGCTTATGGTGGGTGACCGCCTGGAGACCGAC A G Z83844.3,PDXP Ensembl:ENSG00000285304,Ensembl:ENSG00000241360 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:37665551..37666181 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_579566,Human_RBP_ID_9300387,Human_RBP_ID_9333360,Human_RBP_ID_22269624,Human_RBP_ID_22507988,Human_RBP_ID_23946528 RMVar_hsa_circ_117648,RMVar_hsa_circ_214180,RMVar_hsa_circ_214181,RMVar_hsa_circ_114542,RMVar_hsa_circ_81114,RMVar_hsa_circ_98260,RMVar_hsa_circ_214183,RMVar_hsa_circ_91112,RMVar_hsa_circ_214184,RMVar_hsa_circ_79359,RMVar_hsa_circ_109908,RMVar_hsa_circ_214185,RMVar_hsa_circ_214186,RMVar_hsa_circ_214187,RMVar_hsa_circ_127653,RMVar_hsa_circ_98281,RMVar_hsa_circ_214190,RMVar_hsa_circ_214191 112208 RMVar_ID_112208 Human_SNP_ID_844540194 m1A Human chr22 + 37568216 37568216 37568216 CTTCCCCTCTGAGCCCGGGCTTCGCCGCTCTGACTCTCTCTTGTCCTTCCGCCTGGACCTCGACC CTTCCCCTCTGAGCCCGGGCTTCGCCGCTCTGGCTCTCTCTTGTCCTTCCGCCTGGACCTCGACC A G CDC42EP1 Ensembl:ENSG00000128283 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37568101..37568450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_781530,Human_RBP_ID_2718073,Human_RBP_ID_9332833,Human_RBP_ID_17400023,Human_RBP_ID_18952599,Human_RBP_ID_22533836,Human_RBP_ID_27307562,Human_RBP_ID_27493689 RMVar_hsa_circ_108972,RMVar_hsa_circ_79438,RMVar_hsa_circ_214164,RMVar_hsa_circ_113182,RMVar_hsa_circ_214165,RMVar_hsa_circ_214166 112209 RMVar_ID_112209 Human_SNP_ID_844545838 m1A Human chr22 - 30340793 30340790 30340793 CTTTGCTTTTCAGGGTTCAGATGATGAAGAAGAAGGGCAGAAAGTGCCCCCACCCCCAGAGACAC CTTTGCTTTTCAGGGTTCAGATGATGAAGAAG___GGCAGAAAGTGCCCCCACCCCCAGAGACAC CCTT C SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:30340667..30340843 26863196 MeRIP-seq:(Medium) rs1449715093 Functional Loss DEL TCGA,ICGC 33..35 33 STAD,LIHC 2 - Human_RBP_ID_64919,Human_RBP_ID_1609950,Human_RBP_ID_8548343,Human_RBP_ID_17989190,Human_RBP_ID_26345297 Human_Splice_Rec_2153070,Human_Splice_Rec_2153071,Human_Splice_Rec_2153094,Human_Splice_Rec_2153095 RMVar_hsa_circ_101369,RMVar_hsa_circ_106607,RMVar_hsa_circ_213741,RMVar_hsa_circ_97623,RMVar_hsa_circ_213742,RMVar_hsa_circ_213740 112210 RMVar_ID_112210 Human_SNP_ID_844564279 m1A Human chr22 + 29674904 29674904 29674904 GGAAGCACGCGAGGCGGAGCGAAGAGCCAAGCAGAAGCTCCTGGAGATTGCCACCAAGCCCACGT GGAAGCACGCGAGGCGGAGCGAAGAGCCAAGCTGAAGCTCCTGGAGATTGCCACCAAGCCCACGT A T NF2 Ensembl:ENSG00000186575 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:29674853..29674985 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 10 lung Human_Splice_Rec_2151696,Human_Splice_Rec_2151697,Human_Splice_Rec_2151726,Human_Splice_Rec_2151727,Human_Splice_Rec_2151758,Human_Splice_Rec_2151759,Human_Splice_Rec_2151790,Human_Splice_Rec_2151791,Human_Splice_Rec_2151822,Human_Splice_Rec_2151823,Human_Splice_Rec_2151852,Human_Splice_Rec_2151853,Human_Splice_Rec_2151882,Human_Splice_Rec_2151883,Human_Splice_Rec_2151910,Human_Splice_Rec_2151911,Human_Splice_Rec_2151938,Human_Splice_Rec_2151939,Human_Splice_Rec_2151956,Human_Splice_Rec_2151957,Human_Splice_Rec_2151982,Human_Splice_Rec_2151983,Human_Splice_Rec_2152014,Human_Splice_Rec_2152015,Human_Splice_Rec_2152048,Human_Splice_Rec_2152049,Human_Splice_Rec_2152068,Human_Splice_Rec_2152069 RMVar_hsa_circ_28274,RMVar_hsa_circ_39428,RMVar_hsa_circ_213661,RMVar_hsa_circ_73862,RMVar_hsa_circ_71457,RMVar_hsa_circ_7241 112211 RMVar_ID_112211 Human_SNP_ID_844564292 m1A Human chr22 + 29674904 29674904 29674904 GGAAGCACGCGAGGCGGAGCGAAGAGCCAAGCAGAAGCTCCTGGAGATTGCCACCAAGCCCACGT GGAAGCACGCGAGGCGGAGCGAAGAGCCAAGCGGAAGCTCCTGGAGATTGCCACCAAGCCCACGT A G NF2 Ensembl:ENSG00000186575 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr22:29674853..29674985 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine ulcerative_colitis 10 large intestine Human_Splice_Rec_2151696,Human_Splice_Rec_2151697,Human_Splice_Rec_2151726,Human_Splice_Rec_2151727,Human_Splice_Rec_2151758,Human_Splice_Rec_2151759,Human_Splice_Rec_2151790,Human_Splice_Rec_2151791,Human_Splice_Rec_2151822,Human_Splice_Rec_2151823,Human_Splice_Rec_2151852,Human_Splice_Rec_2151853,Human_Splice_Rec_2151882,Human_Splice_Rec_2151883,Human_Splice_Rec_2151910,Human_Splice_Rec_2151911,Human_Splice_Rec_2151938,Human_Splice_Rec_2151939,Human_Splice_Rec_2151956,Human_Splice_Rec_2151957,Human_Splice_Rec_2151982,Human_Splice_Rec_2151983,Human_Splice_Rec_2152014,Human_Splice_Rec_2152015,Human_Splice_Rec_2152048,Human_Splice_Rec_2152049,Human_Splice_Rec_2152068,Human_Splice_Rec_2152069 RMVar_hsa_circ_28274,RMVar_hsa_circ_39428,RMVar_hsa_circ_213661,RMVar_hsa_circ_73862,RMVar_hsa_circ_71457,RMVar_hsa_circ_7241 112212 RMVar_ID_112212 Human_SNP_ID_844567549 m1A Human chr22 + 49927391 49927391 49927391 TGGCCCTGAGGATGCCGTCTCCTGCAGTGGACAGCGGCGGGGAGAGGCTGCCTGCTCTCTAACGG TGGCCCTGAGGATGCCGTCTCCTGCAGTGGACCGCGGCGGGGAGAGGCTGCCTGCTCTCTAACGG A C CRELD2 Ensembl:ENSG00000184164 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49927340..49927441 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney Human_RBP_ID_583200,Human_RBP_ID_5120125,Human_RBP_ID_9392523,Human_RBP_ID_17660673 112213 RMVar_ID_112213 Human_SNP_ID_844576173 m1A Human chr22 - 42512864 42512864 42512864 CAGTGAATGGCTGGAGGTGCAGGGCCAGGAGGAGGCGAGGCAGGGCCTGCAGCGGTCTCTGAGAG CAGTGAATGGCTGGAGGTGCAGGGCCAGGAGGCGGCGAGGCAGGGCCTGCAGCGGTCTCTGAGAG T G RRP7A Ensembl:ENSG00000189306 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:42512776..42514213 26863410 MeRIP-seq:(Medium) rs9745 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_246785,Human_RBP_ID_7088965,Human_RBP_ID_27309574 GWAS_ID_6865,GWAS_ID_6866,GWAS_ID_6867,GWAS_ID_6868,GWAS_ID_6869,GWAS_ID_6870,GWAS_ID_6871,GWAS_ID_6872,GWAS_ID_6873,GWAS_ID_6874,GWAS_ID_6875,GWAS_ID_6876,GWAS_ID_6877,GWAS_ID_6878,GWAS_ID_6879 112214 RMVar_ID_112214 Human_SNP_ID_844579258 m1A Human chr22 - 23766269 23766269 23766269 TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCACCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG TGCAGCCTCTTGCACTGTACCCCCAGGCCCCCCCCCCCGCTGCCCCCCAGCCCCTGCAGATGGGG T G CHCHD10 Ensembl:ENSG00000250479 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs767301039 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_2144148,Human_Splice_Rec_2144154,Human_Splice_Rec_2144160,Human_Splice_Rec_2144168 Human_miRNA_ID_1359320,Human_miRNA_ID_2686590 RMVar_hsa_circ_95843,RMVar_hsa_circ_106045,RMVar_hsa_circ_213286,RMVar_hsa_circ_213287 112215 RMVar_ID_112215 Human_SNP_ID_844581342 m1A Human chr22 + 19763454 19763454 19763454 AAGGGTCGTCTGCACCATGAAACTCTTTAGGCACCTGCGATGCTGCCCGATCAACCCGCTCCCTC AAGGGTCGTCTGCACCATGAAACTCTTTAGGCTCCTGCGATGCTGCCCGATCAACCCGCTCCCTC A T TBX1 Ensembl:ENSG00000184058 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:19763450..19763551 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_14396058 112216 RMVar_ID_112216 Human_SNP_ID_844582786 m1A Human chr22 - 43173812 43173812 43173812 AGCCCTTCTGCTCCCCAGGGGCGAGGACAACCACTGGATCTGCAAGCCCTGGAACCTGGCGCGCA AGCCCTTCTGCTCCCCAGGGGCGAGGACAACCGCTGGATCTGCAAGCCCTGGAACCTGGCGCGCA T C TTLL12 Ensembl:ENSG00000100304 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:43173697..43173877 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_834039,Human_RBP_ID_4703400,Human_RBP_ID_8864726,Human_RBP_ID_22454515,Human_RBP_ID_26822654 Human_Splice_Rec_2173342,Human_Splice_Rec_2173343 RMVar_hsa_circ_120351,RMVar_hsa_circ_103225,RMVar_hsa_circ_32663,RMVar_hsa_circ_87082,RMVar_hsa_circ_95645,RMVar_hsa_circ_214868,RMVar_hsa_circ_214869,RMVar_hsa_circ_214870,RMVar_hsa_circ_214867,RMVar_hsa_circ_63976,RMVar_hsa_circ_214871,RMVar_hsa_circ_292542,RMVar_hsa_circ_313256 112217 RMVar_ID_112217 Human_SNP_ID_844591342 m1A Human chr22 - 42636837 42636837 42636837 CCCCGCGGGTCCTGTCGTTTCAGTTGGGCCATATGGTGCTCTTCCCAGTCTGGTTCCTGTACAGT CCCCGCGGGTCCTGTCGTTTCAGTTGGGCCATGTGGTGCTCTTCCCAGTCTGGTTCCTGTACAGT T C CYB5R3 Ensembl:ENSG00000100243 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:42636701..42636907 26863410 MeRIP-seq:(Medium) rs147001900 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 7 head and neck Human_RBP_ID_65154,Human_RBP_ID_246576,Human_RBP_ID_582230,Human_RBP_ID_1308314,Human_RBP_ID_2721111,Human_RBP_ID_4709141 Human_Splice_Rec_2172830,Human_Splice_Rec_2172846,Human_Splice_Rec_2172862,Human_Splice_Rec_2172904,Human_Splice_Rec_2172920,Human_Splice_Rec_2172930 Human_miRNA_ID_2301973,Human_miRNA_ID_2305235,Human_miRNA_ID_2308501 RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591,RMVar_hsa_circ_352613,RMVar_hsa_circ_214810,RMVar_hsa_circ_214809 112218 RMVar_ID_112218 Human_SNP_ID_844605908 m1A Human chr22 - 36285322 36285322 36285322 AAGGTCACTGGCCCTTCTTCTGCAGATCGACCAGATCAACACCGACCTGAACCTGGAGCGCAGCC AAGGTCACTGGCCCTTCTTCTGCAGATCGACCTGATCAACACCGACCTGAACCTGGAGCGCAGCC T A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36285301..36285350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_Splice_Rec_2162520,Human_Splice_Rec_2162530,Human_Splice_Rec_2162538 RMVar_hsa_circ_214052,RMVar_hsa_circ_91840,RMVar_hsa_circ_125248,RMVar_hsa_circ_126947,RMVar_hsa_circ_122213,RMVar_hsa_circ_112195,RMVar_hsa_circ_107935,RMVar_hsa_circ_110705,RMVar_hsa_circ_100473,RMVar_hsa_circ_90265,RMVar_hsa_circ_90568,RMVar_hsa_circ_214054,RMVar_hsa_circ_214055,RMVar_hsa_circ_214053,RMVar_hsa_circ_214048,RMVar_hsa_circ_214050,RMVar_hsa_circ_214051,RMVar_hsa_circ_214049,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_65834,RMVar_hsa_circ_75874,RMVar_hsa_circ_95666,RMVar_hsa_circ_105916,RMVar_hsa_circ_214058,RMVar_hsa_circ_214059,RMVar_hsa_circ_108000,RMVar_hsa_circ_112684,RMVar_hsa_circ_106579,RMVar_hsa_circ_214062,RMVar_hsa_circ_214063,RMVar_hsa_circ_214064,RMVar_hsa_circ_214061 112219 RMVar_ID_112219 Human_SNP_ID_844606969 m1A Human chr22 - 29299297 29299297 29299297 GGGGGCGGAAAGGGTGGCGGGAGGAAGCCTTCAGGCTTTGGGGCCTTACACTGGTTGCACTCTGT GGGGGCGGAAAGGGTGGCGGGAGGAAGCCTTCCGGCTTTGGGGCCTTACACTGGTTGCACTCTGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29299246..29299367 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 9 lung 112220 RMVar_ID_112220 Human_SNP_ID_844613200 m1A Human chr22 + 41177409 41177409 41177409 GGACTCAAGCTGCTGGCCCTGTGTCCCAGGGTAAGGCAGCAGGCCAGGTGACCCCTCCAACCCCT GGACTCAAGCTGCTGGCCCTGTGTCCCAGGGTTAGGCAGCAGGCCAGGTGACCCCTCCAACCCCT A T EP300 Ensembl:ENSG00000100393 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:41177358..41177600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18953076 Human_miRNA_ID_2513531,Human_miRNA_ID_3056352 RMVar_hsa_circ_267084,RMVar_hsa_circ_96540,RMVar_hsa_circ_214579 112221 RMVar_ID_112221 Human_SNP_ID_844617941 m1A Human chr22 - 40856583 40856583 40856583 GCGGTCACGCCGAGCCAGCGCCTGGGCCTGGAACCGGGCCGTAGCCCCCCCAGTTTCGCCCACCA GCGGTCACGCCGAGCCAGCGCCTGGGCCTGGATCCGGGCCGTAGCCCCCCCAGTTTCGCCCACCA T A ST13 Ensembl:ENSG00000100380 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:40856426..40856788;chr22:40856426..40856789 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_581217,Human_RBP_ID_782314,Human_RBP_ID_4708678,Human_RBP_ID_17399855,Human_RBP_ID_22085486,Human_RBP_ID_22270858 112222 RMVar_ID_112222 Human_SNP_ID_844619461 m1A Human chr22 - 40191406 40191406 40191406 GTTTATTCTATTTCTTCTGCCTGAAACAGAGCAGGGAAGAGACCTGGGAAACATCCAATTCCAGT GTTTATTCTATTTCTTCTGCCTGAAACAGAGCGGGGAAGAGACCTGGGAAACATCCAATTCCAGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:40191399..40191482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 112223 RMVar_ID_112223 Human_SNP_ID_844620551 m1A Human chr22 + 39318559 39318559 39318559 GCTGCTGCGCTTCCGAGGCAGGAAGCCGAGGGACCCATGTCTGGGAGCGGAGAACTTTCTGTGAG GCTGCTGCGCTTCCGAGGCAGGAAGCCGAGGGGCCCATGTCTGGGAGCGGAGAACTTTCTGTGAG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr22:39318476..39318625 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 112224 RMVar_ID_112224 Human_SNP_ID_844621170 m1A Human chr22 - 49960957 49960957 49960957 CCCGCAGAGGTGCGCCAGGGAGCCGAACTTGGAGAGCAGCATCGCGGGCGACGGCCTCCCCGGAG CCCGCAGAGGTGCGCCAGGGAGCCGAACTTGGGGAGCAGCATCGCGGGCGACGGCCTCCCCGGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:49960906..49961005 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 112225 RMVar_ID_112225 Human_SNP_ID_844622480 m1A Human chr22 - 50604894 50604894 50604894 CCCCGCCGCTGTCCTCTTCGCTGTCGTGGCCCAGCCCAGCACAGCGCCGCAGGCTCACCAGCTCC CCCCGCCGCTGTCCTCTTCGCTGTCGTGGCCCGGCCCAGCACAGCGCCGCAGGCTCACCAGCTCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:50604723..50604984 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 112226 RMVar_ID_112226 Human_SNP_ID_844623213 m1A Human chr22 + 40850874 40850874 40850874 TTAGCTTTCTGAGTAGCAGGTGGTACTTTACCACCCATGCTTGAAGAAGATGAGAAAAAAGATAT TTAGCTTTCTGAGTAGCAGGTGGTACTTTACCTCCCATGCTTGAAGAAGATGAGAAAAAAGATAT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr22:40850826..40850933;chr22:40850826..40850986;chr22:40850826..40850900;chr22:40850826..40854591;chr22:40850826..40856722 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver 112227 RMVar_ID_112227 Human_SNP_ID_844627486 m1A Human chr22 + 31140308 31140308 31140308 ACCAGCGGAGGGCAGGGGAGCCCCCCAGGGCCACCCCCAGGAAGCCCAGCATCCCAAACAGCCCT ACCAGCGGAGGGCAGGGGAGCCCCCCAGGGCCGCCCCCAGGAAGCCCAGCATCCCAAACAGCCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:31140260..31140422 26863196 MeRIP-seq:(Medium) rs1319887624 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 112228 RMVar_ID_112228 Human_SNP_ID_844630050 m1A Human chr22 + 19766762 19766762 19766762 CATCCGCACCACCACCACCACCCCGTGAGTCCAGCCGCCGCGGCCGCCGCCGCCGCTGCCGCAGC CATCCGCACCACCACCACCACCCCGTGAGTCCGGCCGCCGCGGCCGCCGCCGCCGCTGCCGCAGC A G TBX1 Ensembl:ENSG00000184058 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:19766662..19766763 26863410 MeRIP-seq:(Medium) rs553461195 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 112229 RMVar_ID_112229 Human_SNP_ID_844631372 m1A Human chr22 - 23793655 23793655 23793655 TGAGGTAGGTGGGGGGCTCTGTGCTGATGGACACAGCCTTGTACTTCTCATCGTTGCCATCCAGA TGAGGTAGGTGGGGGGCTCTGTGCTGATGGACCCAGCCTTGTACTTCTCATCGTTGCCATCCAGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:23793604..23793737 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 112230 RMVar_ID_112230 Human_SNP_ID_844633613 m1A Human chr22 - 30339188 30339188 30339188 GGCTGAGCGGCGTACTGACATCTTCGGTGTAGAGGAAACAGCCATTGGTAAGAAGATCGGTGAGG GGCTGAGCGGCGTACTGACATCTTCGGTGTAGTGGAAACAGCCATTGGTAAGAAGATCGGTGAGG T A SF3A1 Ensembl:ENSG00000099995 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:30338951..30339275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 2 lung Human_RBP_ID_782156,Human_RBP_ID_1028931,Human_RBP_ID_1609944,Human_RBP_ID_1941545,Human_RBP_ID_3671072,Human_RBP_ID_7074290,Human_RBP_ID_8862632,Human_RBP_ID_9300669,Human_RBP_ID_9392163,Human_RBP_ID_14452463,Human_RBP_ID_17514710,Human_RBP_ID_27821222 Human_Splice_Rec_2153074,Human_Splice_Rec_2153075,Human_Splice_Rec_2153089,Human_Splice_Rec_2153102,Human_Splice_Rec_2153103,Human_Splice_Rec_2153106 112231 RMVar_ID_112231 Human_SNP_ID_844636049 m1A Human chr22 + 20582666 20582666 20582666 GCTGTCCTCGCCGTCACCGGGCCAGCAGGTGCAGACCCCGCAGTCGATGCCCCCTCCCCCCCAGC GCTGTCCTCGCCGTCACCGGGCCAGCAGGTGCTGACCCCGCAGTCGATGCCCCCTCCCCCCCAGC A T MED15 Ensembl:ENSG00000099917 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:20582566..20582963 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_5133027,Human_RBP_ID_17087401,Human_RBP_ID_17399697,Human_RBP_ID_18952384,Human_RBP_ID_22533804 Human_Splice_Rec_2139750,Human_Splice_Rec_2139751,Human_Splice_Rec_2139792,Human_Splice_Rec_2139793,Human_Splice_Rec_2139826,Human_Splice_Rec_2139827,Human_Splice_Rec_2139866,Human_Splice_Rec_2139867,Human_Splice_Rec_2139896,Human_Splice_Rec_2139897,Human_Splice_Rec_2140008,Human_Splice_Rec_2140009,Human_Splice_Rec_2140032,Human_Splice_Rec_2140033,Human_Splice_Rec_2140049 Human_miRNA_ID_466161 RMVar_hsa_circ_265322 112232 RMVar_ID_112232 Human_SNP_ID_844643002 m1A Human chr22 + 35257551 35257551 35257551 CGGCGGCGTTGAGGCGGGATCCGGGCGAGCCGAGTGAAGGTAGCGGCGAGCGGAGACCCCAGGAG CGGCGGCGTTGAGGCGGGATCCGGGCGAGCCGCGTGAAGGTAGCGGCGAGCGGAGACCCCAGGAG A C HMGXB4 Ensembl:ENSG00000100281 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:35257501..35257698 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_246587,Human_RBP_ID_19113158,Human_RBP_ID_26345339,Human_RBP_ID_27821630 Human_Splice_Rec_2161265,Human_Splice_Rec_2161271,Human_Splice_Rec_2161293,Human_Splice_Rec_2161295,Human_Splice_Rec_2161315 112233 RMVar_ID_112233 Human_SNP_ID_844647108 m1A Human chr22 + 47136760 47136760 47136760 ACCAGGACTGCTGAGGTGAGCAAGGACAGTGGACGTCACTGCCTGTGCCCCCAGGACACCTGTGG ACCAGGACTGCTGAGGTGAGCAAGGACAGTGGGCGTCACTGCCTGTGCCCCCAGGACACCTGTGG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:47136755..47136855 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_26762512 112234 RMVar_ID_112234 Human_SNP_ID_844648722 m1A Human chr22 + 30337818 30337818 30337818 GCGGCATGGGGGCGATCACTGAGCCTGGGGGCAGCCGGACCACAGATGCCATTGGGGGCCGGGGC GCGGCATGGGGGCGATCACTGAGCCTGGGGGCGGCCGGACCACAGATGCCATTGGGGGCCGGGGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:30337631..30337918 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 2 liver 112235 RMVar_ID_112235 Human_SNP_ID_844651960 m1A Human chr22 - 36300266 36300266 36300266 CTGCTGTCCTTACCGTGTCTCTGGCCCCCGGCAGGAGCTTGAGGAGCAGCTGGAGGAGGAGGAGA CTGCTGTCCTTACCGTGTCTCTGGCCCCCGGCGGGAGCTTGAGGAGCAGCTGGAGGAGGAGGAGA T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:36300226..36300275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_10681,Human_RBP_ID_65268,Human_RBP_ID_152118 RMVar_hsa_circ_91840,RMVar_hsa_circ_122213,RMVar_hsa_circ_107935,RMVar_hsa_circ_214048,RMVar_hsa_circ_214046,RMVar_hsa_circ_214047,RMVar_hsa_circ_95666,RMVar_hsa_circ_214059,RMVar_hsa_circ_95492,RMVar_hsa_circ_122436,RMVar_hsa_circ_214066,RMVar_hsa_circ_123651,RMVar_hsa_circ_214067,RMVar_hsa_circ_214069,RMVar_hsa_circ_81767,RMVar_hsa_circ_214072,RMVar_hsa_circ_109659,RMVar_hsa_circ_117583,RMVar_hsa_circ_214075,RMVar_hsa_circ_41876,RMVar_hsa_circ_89,RMVar_hsa_circ_96166,RMVar_hsa_circ_104640,RMVar_hsa_circ_214076,RMVar_hsa_circ_214078,RMVar_hsa_circ_73354,RMVar_hsa_circ_214079,RMVar_hsa_circ_36127,RMVar_hsa_circ_1430,RMVar_hsa_circ_25411,RMVar_hsa_circ_93690,RMVar_hsa_circ_214080 112236 RMVar_ID_112236 Human_SNP_ID_844655784 m1A Human chr22 + 44323685 44323685 44323685 ATCCATCCATCCATCCATCCATCCATCCATCCATCCATCTATCATCCCTTCATTCTCAGCAACCT ATCCATCCATCCATCCATCCATCCATCCATCCTTCCATCTATCATCCCTTCATTCTCAGCAACCT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:44323683..44323780 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 112237 RMVar_ID_112237 Human_SNP_ID_844667154 m1A Human chr22 + 41622064 41622064 41622064 ACCGAGGGCGATGAAGAAGCAGAGGAAGAACAAGAAGAGAACCTTGAAGCAAGTGGTAAGTGACT ACCGAGGGCGATGAAGAAGCAGAGGAAGAACAGGAAGAGAACCTTGAAGCAAGTGGTAAGTGACT A G XRCC6 Ensembl:ENSG00000196419 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:41621976..41622129 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 8 lung Human_RBP_ID_246786,Human_RBP_ID_1612781,Human_RBP_ID_1943784,Human_RBP_ID_4709347,Human_RBP_ID_7087348,Human_RBP_ID_8117550,Human_RBP_ID_9392435,Human_RBP_ID_14508352,Human_RBP_ID_18535227,Human_RBP_ID_18544720,Human_RBP_ID_18790474,Human_RBP_ID_23015625,Human_RBP_ID_24381868,Human_RBP_ID_24547074,Human_RBP_ID_26344939,Human_RBP_ID_27821724 Human_Splice_Rec_2171050,Human_Splice_Rec_2171051,Human_Splice_Rec_2171074,Human_Splice_Rec_2171075,Human_Splice_Rec_2171096,Human_Splice_Rec_2171097,Human_Splice_Rec_2171100,Human_Splice_Rec_2171101,Human_Splice_Rec_2171123,Human_Splice_Rec_2171145,Human_Splice_Rec_2171167 RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 112238 RMVar_ID_112238 Human_SNP_ID_844672012 m1A Human chr22 + 29297875 29297875 29297875 GAGCAAACTTAAAGTCTCCCTTGCTCGGAAGAAGCCTCCAATGAACAGTATGCGGGGTGGTCTGC GAGCAAACTTAAAGTCTCCCTTGCTCGGAAGAGGCCTCCAATGAACAGTATGCGGGGTGGTCTGC A G EWSR1 Ensembl:ENSG00000182944 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:29296251..29297876 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 2 - Human_RBP_ID_1609723,Human_RBP_ID_1941362,Human_RBP_ID_3670764,Human_RBP_ID_3962291,Human_RBP_ID_7072707,Human_RBP_ID_8862375,Human_RBP_ID_9125543,Human_RBP_ID_9260679,Human_RBP_ID_9392108,Human_RBP_ID_14445032,Human_RBP_ID_18786769,Human_RBP_ID_19007832,Human_RBP_ID_22454402,Human_RBP_ID_23941997 Human_Splice_Rec_2150464,Human_Splice_Rec_2150465,Human_Splice_Rec_2150492,Human_Splice_Rec_2150493,Human_Splice_Rec_2150524,Human_Splice_Rec_2150525,Human_Splice_Rec_2150588,Human_Splice_Rec_2150589,Human_Splice_Rec_2150640,Human_Splice_Rec_2150641,Human_Splice_Rec_2150688,Human_Splice_Rec_2150689,Human_Splice_Rec_2150746,Human_Splice_Rec_2150747,Human_Splice_Rec_2150774,Human_Splice_Rec_2150775,Human_Splice_Rec_2150788,Human_Splice_Rec_2150789,Human_Splice_Rec_2150802,Human_Splice_Rec_2150803,Human_Splice_Rec_2150814,Human_Splice_Rec_2150815,Human_Splice_Rec_2150824,Human_Splice_Rec_2150825 RMVar_hsa_circ_38608,RMVar_hsa_circ_53612 112239 RMVar_ID_112239 Human_SNP_ID_844676991 m1A Human chr22 + 45240858 45240858 45240858 CTGTGCGCGTCGCCGTCGCCGCCGCCGCCGCCACCACCCGCCAAACACAGCACCGGCGAGCGCAC CTGTGCGCGTCGCCGTCGCCGCCGCCGCCGCCGCCACCCGCCAAACACAGCACCGGCGAGCGCAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr22:45240788..45240901 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - 112240 RMVar_ID_112240 Human_SNP_ID_844678324 m1A Human chr22 - 38485418 38485418 38485418 ATTGCCCTGCACATTTTCTTTTGTGCTTTTAAATGTTTCTTAAGTTGGAACAGGTTTCCTCGGGC ATTGCCCTGCACATTTTCTTTTGTGCTTTTAAGTGTTTCTTAAGTTGGAACAGGTTTCCTCGGGC T C DDX17 Ensembl:ENSG00000100201 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_65066,Human_RBP_ID_580209,Human_RBP_ID_1029354,Human_RBP_ID_1307917,Human_RBP_ID_1611591,Human_RBP_ID_1942792,Human_RBP_ID_2718693,Human_RBP_ID_3672792,Human_RBP_ID_7081556,Human_RBP_ID_8208635,Human_RBP_ID_10051854,Human_RBP_ID_14485485,Human_RBP_ID_17515205,Human_RBP_ID_17986166,Human_RBP_ID_23013215,Human_RBP_ID_23947475,Human_RBP_ID_24494143,Human_RBP_ID_25670063,Human_RBP_ID_27037588 Human_miRNA_ID_1433478,Human_miRNA_ID_1717081,Human_miRNA_ID_2732380 RMVar_hsa_circ_86804,RMVar_hsa_circ_99912,RMVar_hsa_circ_102735,RMVar_hsa_circ_123007,RMVar_hsa_circ_101987,RMVar_hsa_circ_92471,RMVar_hsa_circ_98657,RMVar_hsa_circ_90980,RMVar_hsa_circ_214295,RMVar_hsa_circ_214299,RMVar_hsa_circ_214301,RMVar_hsa_circ_80727,RMVar_hsa_circ_214302,RMVar_hsa_circ_214300,RMVar_hsa_circ_214297,RMVar_hsa_circ_214298,RMVar_hsa_circ_214296,RMVar_hsa_circ_214294 112241 RMVar_ID_112241 Human_SNP_ID_844681265 m1A Human chr22 - 20139567 20139567 20139567 GCGCGGCGGGCGGTAGAAGTGGCACGTGGCACACCACTTCATGCGGACCTGGATACCTCGCACAT GCGCGGCGGGCGGTAGAAGTGGCACGTGGCACGCCACTTCATGCGGACCTGGATACCTCGCACAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:20139520..20139633 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 112242 RMVar_ID_112242 Human_SNP_ID_844688461 m1A Human chr22 - 50278205 50278205 50278205 GCACCTGGTGCGGCCGACCGACGAGGTGGACGAGGGCAAGTCCAAGAGAGGCAGCGTGAAAGAGA GCACCTGGTGCGGCCGACCGACGAGGTGGACGCGGGCAAGTCCAAGAGAGGCAGCGTGAAAGAGA T G PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:50277851..50278525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung Human_Splice_Rec_2179772,Human_Splice_Rec_2179773,Human_Splice_Rec_2179808,Human_Splice_Rec_2179809,Human_Splice_Rec_2179848,Human_Splice_Rec_2179849,Human_Splice_Rec_2179920,Human_Splice_Rec_2179921,Human_Splice_Rec_2179992,Human_Splice_Rec_2179993,Human_Splice_Rec_2180024,Human_Splice_Rec_2180025,Human_Splice_Rec_2180050,Human_Splice_Rec_2180051,Human_Splice_Rec_2180060,Human_Splice_Rec_2180061 RMVar_hsa_circ_84415,RMVar_hsa_circ_117661,RMVar_hsa_circ_126413,RMVar_hsa_circ_120066,RMVar_hsa_circ_120497,RMVar_hsa_circ_118046,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_79920,RMVar_hsa_circ_215257,RMVar_hsa_circ_215254,RMVar_hsa_circ_215255,RMVar_hsa_circ_215253,RMVar_hsa_circ_215250,RMVar_hsa_circ_215251,RMVar_hsa_circ_215249,RMVar_hsa_circ_6760,RMVar_hsa_circ_215264,RMVar_hsa_circ_111551,RMVar_hsa_circ_116182,RMVar_hsa_circ_96247,RMVar_hsa_circ_215265,RMVar_hsa_circ_215262,RMVar_hsa_circ_215263,RMVar_hsa_circ_127466,RMVar_hsa_circ_215266,RMVar_hsa_circ_90600,RMVar_hsa_circ_215267 112243 RMVar_ID_112243 Human_SNP_ID_844696852 m1A Human chr22 + 31944586 31944578 31944586 AGCGAGAGGGCGCGAGCGGCGGCGCTGCCTGCAGCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG AGCGAGAGGGCGCGAGCGGCGGCGC________GCCTGCAGCCTGCAGCCTCCGGCCGGCCGGCG CTGCCTGCA C YWHAH,Z82190.2 Ensembl:ENSG00000128245,Ensembl:ENSG00000285404 Protein coding,Protein coding 5'UTR,intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31944550..31944640 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 26..33 33 SKCA 1 - Human_RBP_ID_781510,Human_RBP_ID_833778,Human_RBP_ID_4708151,Human_RBP_ID_5240830,Human_RBP_ID_8943160,Human_RBP_ID_9332797,Human_RBP_ID_18423639 Human_miRNA_ID_3052743 112244 RMVar_ID_112244 Human_SNP_ID_844699867 m1A Human chr22 + 36511786 36511786 36511786 GAGGAGTCTTTCACGTGGTACCGAGACACATAACTAACAGGGGAAGGGATATCAGTGGTCAGAGC GAGGAGTCTTTCACGTGGTACCGAGACACATACCTAACAGGGGAAGGGATATCAGTGGTCAGAGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:36511751..36511800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 2 skin,head and neck 112245 RMVar_ID_112245 Human_SNP_ID_844701696 m1A Human chr22 - 38204887 38204887 38204887 AAGAGCTGTCAGAGGAATCACTACTGACACAAACCCACGAGCCTGTCCGTGCTTGGCCCATTTCA AAGAGCTGTCAGAGGAATCACTACTGACACAACCCCACGAGCCTGTCCGTGCTTGGCCCATTTCA T G PLA2G6 Ensembl:ENSG00000184381 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:38204885..38204977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112246 RMVar_ID_112246 Human_SNP_ID_844702069 m1A Human chr22 - 37849467 37849467 37849467 CCTTACGGCCACCTTACCTCAGACTCATAATCATCAGCGGGATAAGACATGGCTGCCTCGCTTGC CCTTACGGCCACCTTACCTCAGACTCATAATCGTCAGCGGGATAAGACATGGCTGCCTCGCTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr22:37849426..37849531;chr22:37849426..37849500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 112247 RMVar_ID_112247 Human_SNP_ID_844704162 m1A Human chr22 - 38294167 38294167 38294167 GAGTATGAGGCTGCACAGGGGTGCGCCCGCCAACGTCTCCTCCTCAGACCTCACTGGGCGGCAAG GAGTATGAGGCTGCACAGGGGTGCGCCCGCCAGCGTCTCCTCCTCAGACCTCACTGGGCGGCAAG T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:38294027..38294201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver Human_RBP_ID_580033,Human_RBP_ID_930980,Human_RBP_ID_4697059,Human_RBP_ID_5504810,Human_RBP_ID_17986075,Human_RBP_ID_22820537,Human_RBP_ID_23947207,Human_RBP_ID_26675769,Human_RBP_ID_27821304 Human_Splice_Rec_2166584,Human_Splice_Rec_2166585,Human_Splice_Rec_2166604,Human_Splice_Rec_2166605,Human_Splice_Rec_2166610,Human_Splice_Rec_2166611,Human_Splice_Rec_2166618,Human_Splice_Rec_2166619,Human_Splice_Rec_2166624,Human_Splice_Rec_2166625,Human_Splice_Rec_2166642,Human_Splice_Rec_2166643,Human_Splice_Rec_2166654,Human_Splice_Rec_2166655,Human_Splice_Rec_2166658,Human_Splice_Rec_2166744,Human_Splice_Rec_2166745 Human_miRNA_ID_2371201,Human_miRNA_ID_2707482 RMVar_hsa_circ_13824,RMVar_hsa_circ_278542,RMVar_hsa_circ_378565,RMVar_hsa_circ_58767,RMVar_hsa_circ_214277 112248 RMVar_ID_112248 Human_SNP_ID_844707201 m1A Human chr22 - 29299666 29299666 29299666 CCACGGCCACCTCTGAACATTCCACCGGGACCACCACGATCCATGAGGCCACCTCTTCCTCCCCG CCACGGCCACCTCTGAACATTCCACCGGGACCCCCACGATCCATGAGGCCACCTCTTCCTCCCCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:29299576..29299875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas 112249 RMVar_ID_112249 Human_SNP_ID_844708205 m1A Human chr22 + 41528613 41528613 41528613 GCCCTCAACAGAATGAAGGAACTGCAACAGTGAGGGCAGTGCCTCCCCGCCCCGCCGCTGGCGTC GCCCTCAACAGAATGAAGGAACTGCAACAGTGGGGGCAGTGCCTCCCCGCCCCGCCGCTGGCGTC A G ACO2 Ensembl:ENSG00000100412 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41528565..41528792 26863196 MeRIP-seq:(Medium) rs1569027545 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 24 head and neck Human_RBP_ID_581563,Human_RBP_ID_22454492 Human_miRNA_ID_2389082,Human_miRNA_ID_2476983,Human_miRNA_ID_2962767,Human_miRNA_ID_3022751 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667 112250 RMVar_ID_112250 Human_SNP_ID_844708490 m1A Human chr22 - 38398815 38398815 38398815 GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGACCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC GCCGGACGCGCCGCGCCCTGGCGGCTCTAGGGTCCCCCCCCGCGCCTGCACTTAGCCCCGCGCCC T A TPTEP2 Ensembl:ENSG00000244627 Pseudogene exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:38398783..38398862 26863196 MeRIP-seq:(Medium) rs1027792000 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_18423647,Human_RBP_ID_22270026 Human_Splice_Rec_2166749,Human_Splice_Rec_2166767,Human_Splice_Rec_2166775,Human_Splice_Rec_2166785,Human_Splice_Rec_2166803,Human_Splice_Rec_2166821,Human_Splice_Rec_2166829 112251 RMVar_ID_112251 Human_SNP_ID_844710787 m1A Human chr22 - 37833757 37833757 37833757 TCCGACAACTCCTCTTGGGTTTGCCTGTTTCCAGTGCAGCTGCTCCTGGACCATGGTGCTGATCC TCCGACAACTCCTCTTGGGTTTGCCTGTTTCCGGTGCAGCTGCTCCTGGACCATGGTGCTGATCC T C ANKRD54 Ensembl:ENSG00000100124 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:37833708..37833970 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_4696429,Human_RBP_ID_14478017,Human_RBP_ID_22550750,Human_RBP_ID_22675287 Human_Splice_Rec_2164981,Human_Splice_Rec_2164991,Human_Splice_Rec_2165003,Human_Splice_Rec_2165015,Human_Splice_Rec_2165025,Human_Splice_Rec_2165039,Human_Splice_Rec_2165051,Human_Splice_Rec_2165063,Human_Splice_Rec_2165075,Human_Splice_Rec_2165083,Human_Splice_Rec_2165093 RMVar_hsa_circ_119022,RMVar_hsa_circ_81722,RMVar_hsa_circ_214220,RMVar_hsa_circ_214221,RMVar_hsa_circ_350018 112252 RMVar_ID_112252 Human_SNP_ID_844715283 m1A Human chr22 + 31463054 31463054 31463054 TGGTTTCAGACTGACTTGTGGGTCCAGCAGAGAACCACTCTGGTTCTTCTTCTGTGTAAGAATCA TGGTTTCAGACTGACTTGTGGGTCCAGCAGAGCACCACTCTGGTTCTTCTTCTGTGTAAGAATCA A C AL096701.3,DRG1 Ensembl:ENSG00000240591,Ensembl:ENSG00000185721 lincRNA,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:31463010..31463111 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain 112253 RMVar_ID_112253 Human_SNP_ID_844717694 m1A Human chr22 - 19135072 19135072 19135072 CAAGAAGCAGGAAGCCTTGCGGAGAGTGACGGAGAATCTGGCCAGGTGAGGGGCCGCCTGGCTGG CAAGAAGCAGGAAGCCTTGCGGAGAGTGACGGGGAATCTGGCCAGGTGAGGGGCCGCCTGGCTGG T C ESS2 Ensembl:ENSG00000100056 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:19134246..19135079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_929108,Human_RBP_ID_5119837,Human_RBP_ID_8545447,Human_RBP_ID_19008442 Human_Splice_Rec_2136463,Human_Splice_Rec_2136481,Human_Splice_Rec_2136499 RMVar_hsa_circ_120026,RMVar_hsa_circ_212908 112254 RMVar_ID_112254 Human_SNP_ID_844717789 m1A Human chr22 + 17739415 17739411 17739416 GCCAGGCCGTTCACCAGGCCCGGAGGGATGCTACGGTCCATGCTGTCCCCGACCTGGGCGAGGTG GCCAGGCCGTTCACCAGGCCCGGAGGGAT_____GGTCCATGCTGTCCCCGACCTGGGCGAGGTG TGCTAC T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:17739317..17739486 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 30..34 33 STAD 1 - 112255 RMVar_ID_112255 Human_SNP_ID_844724592 m1A Human chr22 + 49884235 49884235 49884235 TCGTTCCCCTCTCCCTCACTCCTGCTTCCACCACAGCCTGCGGACGCGGGTGACCTCAGCACCAT TCGTTCCCCTCTCCCTCACTCCTGCTTCCACCGCAGCCTGCGGACGCGGGTGACCTCAGCACCAT A G ZBED4 Ensembl:ENSG00000100426 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs910797 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_18194216 Clinvar_Rec_196 GWAS_ID_6894,GWAS_ID_6895,GWAS_ID_6896,GWAS_ID_6897,GWAS_ID_6898,GWAS_ID_6899,GWAS_ID_6900,GWAS_ID_6901,GWAS_ID_6902,GWAS_ID_6903,GWAS_ID_6904,GWAS_ID_6905,GWAS_ID_6906,GWAS_ID_6907,GWAS_ID_6908,GWAS_ID_6909,GWAS_ID_6910,GWAS_ID_6911,GWAS_ID_6912,GWAS_ID_6913,GWAS_ID_6914,GWAS_ID_6915,GWAS_ID_6916,GWAS_ID_6917,GWAS_ID_6918,GWAS_ID_6919,GWAS_ID_6920,GWAS_ID_6921,GWAS_ID_6922,GWAS_ID_6923,GWAS_ID_6924,GWAS_ID_6925,GWAS_ID_6926,GWAS_ID_6927,GWAS_ID_6928 RMVar_hsa_circ_215190 112256 RMVar_ID_112256 Human_SNP_ID_844728079 m1A Human chr22 - 20086131 20086131 20086131 AAGGGGTCCTCAGCAGGGAGTTCGGACTGTCCATCACCACCAGAGCCAACGTCCATTACCTCTGC AAGGGGTCCTCAGCAGGGAGTTCGGACTGTCCGTCACCACCAGAGCCAACGTCCATTACCTCTGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:20085973..20086164 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 skin desmoplastic,MELA 4 skin Human_RBP_ID_5202887 112257 RMVar_ID_112257 Human_SNP_ID_844736305 m1A Human chr22 + 29310923 29310923 29310923 TCCCCGCCCTGCTAGCCCAGTCCCTGGGAGTGAGCGCCGGGGCTCCCGGCCTGAGATGACTCCCG TCCCCGCCCTGCTAGCCCAGTCCCTGGGAGTGGGCGCCGGGGCTCCCGGCCTGAGATGACTCCCG A G GAS2L1 Ensembl:ENSG00000185340 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29310876..29311043 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_Splice_Rec_2150836,Human_Splice_Rec_2150837,Human_Splice_Rec_2150852,Human_Splice_Rec_2150853,Human_Splice_Rec_2150862,Human_Splice_Rec_2150870,Human_Splice_Rec_2150871,Human_Splice_Rec_2150880,Human_Splice_Rec_2150881,Human_Splice_Rec_2150890,Human_Splice_Rec_2150891,Human_Splice_Rec_2150896 RMVar_hsa_circ_378098 112258 RMVar_ID_112258 Human_SNP_ID_844737678 m1A Human chr22 + 39521944 39521944 39521944 CTTTGCCCCCCTAGTCCAGGAGACTAATAAGCAGCCCCCCCAGACGGTGAACCCAATTGGCCATC CTTTGCCCCCCTAGTCCAGGAGACTAATAAGCGGCCCCCCCAGACGGTGAACCCAATTGGCCATC A G ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr22:39521795..39522162;chr22:39521901..39522075;chr22:39521901..39521975 31548705,26863196 m1A-IP-seq:(High) rs146469032 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_65474,Human_RBP_ID_246158,Human_RBP_ID_580924,Human_RBP_ID_781522,Human_RBP_ID_932109,Human_RBP_ID_1029475,Human_RBP_ID_1612186,Human_RBP_ID_1943106,Human_RBP_ID_4712908,Human_RBP_ID_5119939,Human_RBP_ID_7083132,Human_RBP_ID_8550690,Human_RBP_ID_9126770,Human_RBP_ID_14490694,Human_RBP_ID_17286116,Human_RBP_ID_17399302,Human_RBP_ID_17986637,Human_RBP_ID_22087189,Human_RBP_ID_22270629,Human_RBP_ID_22508106,Human_RBP_ID_22821018,Human_RBP_ID_23016201,Human_RBP_ID_23948526,Human_RBP_ID_25671310,Human_RBP_ID_26501122,Human_RBP_ID_27038248,Human_RBP_ID_27308541,Human_RBP_ID_27494333 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 112259 RMVar_ID_112259 Human_SNP_ID_844738871 m1A Human chr22 - 50448446 50448446 50448446 AGCCCTGACCCAAGTCCCAACCTCCTGTTCCCAGGGCACCCCTAGCTCCCTCCTTGTGTCCACCG AGCCCTGACCCAAGTCCCAACCTCCTGTTCCCCGGGCACCCCTAGCTCCCTCCTTGTGTCCACCG T G SBF1 Ensembl:ENSG00000100241 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr22:50448441..50448554;chr22:50448435..50448569 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach RMVar_hsa_circ_93411,RMVar_hsa_circ_95385,RMVar_hsa_circ_96381,RMVar_hsa_circ_215307,RMVar_hsa_circ_215308,RMVar_hsa_circ_215309 112260 RMVar_ID_112260 Human_SNP_ID_844742682 m1A Human chr22 + 22303126 22303126 22303126 GTGTTTCTAGTGATGGGAACAGTGAGAATCAGACTTGGAACACGGAGCGCATTGTGGGCCTGTCG GTGTTTCTAGTGATGGGAACAGTGAGAATCAGGCTTGGAACACGGAGCGCATTGTGGGCCTGTCG A G AC245060.7 Ensembl:ENSG00000286129 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:22303107..22303205 26863196 MeRIP-seq:(Medium) rs199772824 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_14411332 112261 RMVar_ID_112261 Human_SNP_ID_844745948 m1A Human chr22 - 37623605 37623605 37623605 TCACCTAAGGCCTCATCATTGTCCTCTGTGTCACTCGCCAGTCGGAAGAGCGTGGGCCGCATCCG TCACCTAAGGCCTCATCATTGTCCTCTGTGTCGCTCGCCAGTCGGAAGAGCGTGGGCCGCATCCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:37623500..37623625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 112262 RMVar_ID_112262 Human_SNP_ID_844749043 m1A Human chr22 + 29073142 29073142 29073142 GGGGCCCCGCACTGACGGCCCATGGCGCCGCCAGCCGCCCGCCTCGCCCTGCTCTCCGCCGCGGC GGGGCCCCGCACTGACGGCCCATGGCGCCGCCCGCCGCCCGCCTCGCCCTGCTCTCCGCCGCGGC A C KREMEN1 Ensembl:ENSG00000183762 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr22:29073026..29073175;chr22:29073026..29073200;chr22:29073096..29073163 26863410,26863196 MeRIP-seq:(Medium) rs7292708 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 15 head and neck Human_RBP_ID_931843,Human_RBP_ID_4708927 Human_Splice_Rec_2150155,Human_Splice_Rec_2150171 GWAS_ID_11662,GWAS_ID_11663,GWAS_ID_11664,GWAS_ID_11665,GWAS_ID_11666,GWAS_ID_11667,GWAS_ID_11668,GWAS_ID_11669,GWAS_ID_11670,GWAS_ID_11671,GWAS_ID_11672,GWAS_ID_11673,GWAS_ID_11674,GWAS_ID_11675,GWAS_ID_11676,GWAS_ID_11677,GWAS_ID_11678,GWAS_ID_11679,GWAS_ID_11680,GWAS_ID_11681,GWAS_ID_11682,GWAS_ID_11683,GWAS_ID_11684,GWAS_ID_11685,GWAS_ID_11686,GWAS_ID_11687,GWAS_ID_11688 RMVar_hsa_circ_213593,RMVar_hsa_circ_83202 112263 RMVar_ID_112263 Human_SNP_ID_844754666 m1A Human chr22 + 39522028 39522028 39522028 ACCCGACCAGGTTGCCCCCTTCACCTTCTTACAACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT ACCCGACCAGGTTGCCCCCTTCACCTTCTTACTACCTCTTCCCCTTTCCCCAGGGGTCCTGTCCT A T ATF4 Ensembl:ENSG00000128272 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr22:39521905..39522130 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 7 oesophagus Human_RBP_ID_580932,Human_RBP_ID_781523,Human_RBP_ID_1612190,Human_RBP_ID_2719080,Human_RBP_ID_3673111,Human_RBP_ID_5119941,Human_RBP_ID_5424538,Human_RBP_ID_5446580,Human_RBP_ID_5473185,Human_RBP_ID_5504874,Human_RBP_ID_7083134,Human_RBP_ID_8117433,Human_RBP_ID_8207966,Human_RBP_ID_8262374,Human_RBP_ID_8550692,Human_RBP_ID_17020878,Human_RBP_ID_17286117,Human_RBP_ID_17399304,Human_RBP_ID_17515307,Human_RBP_ID_17986638,Human_RBP_ID_18201485,Human_RBP_ID_18516432,Human_RBP_ID_18953053,Human_RBP_ID_20764270,Human_RBP_ID_21937790,Human_RBP_ID_22085393,Human_RBP_ID_22270630,Human_RBP_ID_22821019,Human_RBP_ID_23285656,Human_RBP_ID_23948527,Human_RBP_ID_24494359,Human_RBP_ID_26498709,Human_RBP_ID_27038250,Human_RBP_ID_27308542,Human_RBP_ID_27494336,Human_RBP_ID_27565389 RMVar_hsa_circ_91278,RMVar_hsa_circ_104510,RMVar_hsa_circ_214409,RMVar_hsa_circ_214410 112264 RMVar_ID_112264 Human_SNP_ID_844759206 m1A Human chr22 + 20406232 20406232 20406232 GTGCGGCTCCTGCGGCAAGGCCTTCACCTGCCACTCATCCCTCACCGTGCATGAGAAGATCCACA GTGCGGCTCCTGCGGCAAGGCCTTCACCTGCCGCTCATCCCTCACCGTGCATGAGAAGATCCACA A G ZNF74 Ensembl:ENSG00000185252 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:20406029..20406278 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_4686380,Human_RBP_ID_27032254 RMVar_hsa_circ_213030 112265 RMVar_ID_112265 Human_SNP_ID_844777493 m1A Human chr22 - 20465386 20465384 20465387 GACTGACAAGTACCGCCAGCTTCCATTGGAGAAGGTCTACTCCCTCCTCAGCAGCAATCGCCTGG GACTGACAAGTACCGCCAGCTTCCATTGGAG___GTCTACTCCCTCCTCAGCAGCAATCGCCTGG CCTT C KLHL22 Ensembl:ENSG00000099910 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:20465340..20465441 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 COAD 1 - Human_RBP_ID_575760,Human_RBP_ID_8865557,Human_RBP_ID_22086282 Human_Splice_Rec_2139645 Human_miRNA_ID_2585446,Human_miRNA_ID_2790506,Human_miRNA_ID_2820131 RMVar_hsa_circ_213033,RMVar_hsa_circ_345877,RMVar_hsa_circ_12450,RMVar_hsa_circ_276817,RMVar_hsa_circ_213038,RMVar_hsa_circ_46747,RMVar_hsa_circ_314674,RMVar_hsa_circ_213037,RMVar_hsa_circ_317566,RMVar_hsa_circ_213039 112266 RMVar_ID_112266 Human_SNP_ID_844780200 m1A Human chr22 + 37808137 37808137 37808137 TGAGCGGGTCATCACGTCCCGTCAGGGGCCGCACATCCGCGTGGACGGCGTCTCCGGAGGTAACG TGAGCGGGTCATCACGTCCCGTCAGGGGCCGCTCATCCGCGTGGACGGCGTCTCCGGAGGTAACG A T GCAT Ensembl:ENSG00000100116 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr22:37808002..37809983 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_4709317,Human_RBP_ID_5149518 Human_Splice_Rec_2164913,Human_Splice_Rec_2164931,Human_Splice_Rec_2164947,Human_Splice_Rec_2164953,Human_Splice_Rec_2164957,Human_Splice_Rec_2164961,Human_Splice_Rec_2164967 RMVar_hsa_circ_101795,RMVar_hsa_circ_214213 112267 RMVar_ID_112267 Human_SNP_ID_844784633 m1A Human chr22 - 29349310 29349310 29349310 CCCTGGATGAGCCTGAGGCCCGGGCTGCCATGATCTGGATTGTGGGCGAGTACGCGGAACGGATC CCCTGGATGAGCCTGAGGCCCGGGCTGCCATGCTCTGGATTGTGGGCGAGTACGCGGAACGGATC T G AP1B1 Ensembl:ENSG00000100280 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:29349260..29349335 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 8 brain Human_RBP_ID_833398,Human_RBP_ID_1941383,Human_RBP_ID_3670797,Human_RBP_ID_4691359,Human_RBP_ID_8862405,Human_RBP_ID_9300659,Human_RBP_ID_19008867,Human_RBP_ID_22820081 Human_Splice_Rec_2150934,Human_Splice_Rec_2150935,Human_Splice_Rec_2150974,Human_Splice_Rec_2150975,Human_Splice_Rec_2151016,Human_Splice_Rec_2151017,Human_Splice_Rec_2151060,Human_Splice_Rec_2151061,Human_Splice_Rec_2151098,Human_Splice_Rec_2151099,Human_Splice_Rec_2151136,Human_Splice_Rec_2151137,Human_Splice_Rec_2151184,Human_Splice_Rec_2151185,Human_Splice_Rec_2151194 Human_miRNA_ID_2277330 RMVar_hsa_circ_31198,RMVar_hsa_circ_213620,RMVar_hsa_circ_90876,RMVar_hsa_circ_120891,RMVar_hsa_circ_65037,RMVar_hsa_circ_110133,RMVar_hsa_circ_213621,RMVar_hsa_circ_213622,RMVar_hsa_circ_24725,RMVar_hsa_circ_113751,RMVar_hsa_circ_213623,RMVar_hsa_circ_76181,RMVar_hsa_circ_213626,RMVar_hsa_circ_213627,RMVar_hsa_circ_43749,RMVar_hsa_circ_111671,RMVar_hsa_circ_332980,RMVar_hsa_circ_378515,RMVar_hsa_circ_315193,RMVar_hsa_circ_53865,RMVar_hsa_circ_213628,RMVar_hsa_circ_213629 112268 RMVar_ID_112268 Human_SNP_ID_844788339 m1A Human chr22 - 19962801 19962801 19962801 TGCTGGCCCGGACCCCACCTTTCTTGTCGCCCACGTTCATGGCCCACTCCTTCTGCTCGCAGTAG TGCTGGCCCGGACCCCACCTTTCTTGTCGCCCCCGTTCATGGCCCACTCCTTCTGCTCGCAGTAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr22:19962776..19962800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 8 lung 112269 RMVar_ID_112269 Human_SNP_ID_844789285 m1A Human chr22 - 23767476 23767476 23767476 GGGCTCATGGCTCAGATGGCGACCACGGCCGCAGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT GGGCTCATGGCTCAGATGGCGACCACGGCCGCTGGGGTAGCCGTGGGCTCGGCTGTGGGACACGT T A CHCHD10 Ensembl:ENSG00000250479 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr22:23767426..23767660 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_576527,Human_RBP_ID_1028568,Human_RBP_ID_4708092,Human_RBP_ID_22454580 Human_Splice_Rec_2144166 Human_miRNA_ID_2937811 RMVar_hsa_circ_106045,RMVar_hsa_circ_213286 112270 RMVar_ID_112270 Human_SNP_ID_844791248 m1A Human chr22 + 31276511 31276511 31276511 GCAGGGGACAAAGGGCGGGCGGATCGGCGGGGAGGGGGCGGGGCGCGACCAGGCCAGGCCCGGGG GCAGGGGACAAAGGGCGGGCGGATCGGCGGGGGGGGGGCGGGGCGCGACCAGGCCAGGCCCGGGG A G LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr22:31276509..31276591 26863410 MeRIP-seq:(Medium) rs987847101 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 9 pancreas Human_RBP_ID_3676719,Human_RBP_ID_5120018,Human_RBP_ID_22725104,Human_RBP_ID_26789725 112271 RMVar_ID_112271 Human_SNP_ID_844795498 m1A Human chr22 + 30906001 30906001 30906001 GGCCAATACCGAGAAGCAGCGGCTGGAGGAGAAGCAGCGCCTGTCGCGGCGCCGGCGGCTGGAGG GGCCAATACCGAGAAGCAGCGGCTGGAGGAGAGGCAGCGCCTGTCGCGGCGCCGGCGGCTGGAGG A G OSBP2 Ensembl:ENSG00000184792 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr22:30905950..30906075;chr22:30905951..30906433 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 8 kidney Human_Splice_Rec_2154267,Human_Splice_Rec_2154293,Human_Splice_Rec_2154319,Human_Splice_Rec_2154345,Human_Splice_Rec_2154371,Human_Splice_Rec_2154407,Human_Splice_Rec_2154451,Human_Splice_Rec_2154493,Human_Splice_Rec_2154515,Human_Splice_Rec_2154533 RMVar_hsa_circ_48897,RMVar_hsa_circ_213764 112272 RMVar_ID_112272 Human_SNP_ID_844796082 m1A Human chr22 - 45158364 45158364 45158364 CAAGAGATGTCACCAGTCAATGATGATGGGGCAAAAATTGTTCTGCATTCCGAGGAGGGAGAAAT CAAGAGATGTCACCAGTCAATGATGATGGGGCGAAAATTGTTCTGCATTCCGAGGAGGGAGAAAT T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr22:45158223..45158385 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112273 RMVar_ID_112273 Human_SNP_ID_844800626 m1A Human chr22 - 21629977 21629977 21629977 CCGCCCTCGCATGCGCCTGGTGGTCACCGCGGACGACTTTGGTTACTGCCCGCGACGCGATGAGG CCGCCCTCGCATGCGCCTGGTGGTCACCGCGGGCGACTTTGGTTACTGCCCGCGACGCGATGAGG T C YDJC Ensembl:ENSG00000161179 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr22:21629858..21630025;chr22:21629872..21629977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_1608605,Human_RBP_ID_4687616,Human_RBP_ID_9332717,Human_RBP_ID_22087126 RMVar_hsa_circ_122365,RMVar_hsa_circ_213157 112274 RMVar_ID_112274 Human_SNP_ID_844801908 m1A Human chr22 + 41524922 41524920 41524923 AGAGACCGACTACCTGACGGGCACGGATGGCAAGAAGTTCAGGCTGGAGGCTCCGGATGCAGATG AGAGACCGACTACCTGACGGGCACGGATGGC___AAGTTCAGGCTGGAGGCTCCGGATGCAGATG CAAG C ACO2 Ensembl:ENSG00000100412 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:41524816..41524996 26863196 MeRIP-seq:(Medium) rs750451539 Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_5203053,Human_RBP_ID_8866007,Human_RBP_ID_9300427,Human_RBP_ID_17987300,Human_RBP_ID_22454489 Human_Splice_Rec_2170796,Human_Splice_Rec_2170797,Human_Splice_Rec_2170830,Human_Splice_Rec_2170831 Human_miRNA_ID_2975338,Human_miRNA_ID_3008533,Human_miRNA_ID_3034276 RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_214672,RMVar_hsa_circ_83338,RMVar_hsa_circ_93427,RMVar_hsa_circ_214675,RMVar_hsa_circ_82468,RMVar_hsa_circ_214683,RMVar_hsa_circ_321627 112275 RMVar_ID_112275 Human_SNP_ID_844811635 m1A Human chr22 - 23857957 23857957 23857957 GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGACCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC GGCCTGAGCGGAGGTCTTGCTGTCCCAGGGAGCCCCCGGCTGCCATTAGCAAGCGGTGAGCCGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:23857911..23858002 26863196 MeRIP-seq:(Medium) rs778744344 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 30 biliary tract,gallbladder 112276 RMVar_ID_112276 Human_SNP_ID_844817130 m1A Human chr22 + 38486072 38486072 38486072 TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGACCGGCCTATCCCACTAAACTGCTGGCTAGAGC TTGTGACATCAGTGGCTGTGGCTGCTGCCCAGGCCGGCCTATCCCACTAAACTGCTGGCTAGAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr22:38485926..38486100 26863196 MeRIP-seq:(Medium) rs1391153288 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 112277 RMVar_ID_112277 Human_SNP_ID_844819009 m1A Human chr22 + 20982372 20982372 20982372 TTACAGCGCGGCCGATCCGGCGTGGACCCGGGATGGCTGGACCGGGCAGCACGGGGGGGCAGATC TTACAGCGCGGCCGATCCGGCGTGGACCCGGGTTGGCTGGACCGGGCAGCACGGGGGGGCAGATC A T AC002470.2,LZTR1 Ensembl:ENSG00000285314,Ensembl:ENSG00000099949 lincRNA,Protein coding intron,start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr22:20982321..20982471 26863196 MeRIP-seq:(Medium) rs1569152752 Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 2 breast Human_RBP_ID_3679527,Human_RBP_ID_4708462,Human_RBP_ID_5205827,Human_RBP_ID_5324079,Human_RBP_ID_5600987,Human_RBP_ID_8865860,Human_RBP_ID_9300234,Human_RBP_ID_9332688,Human_RBP_ID_18423699,Human_RBP_ID_23936583,Human_RBP_ID_27841077 RMVar_hsa_circ_87781,RMVar_hsa_circ_213135 112278 RMVar_ID_112278 Human_SNP_ID_844823854 m1A Human chr22 - 37805997 37805997 37805997 GTCTTGGGTTTTTTGGCTTTCTTGGGCGTGGCAGCCAGCTTCTTCTTGGCCTTCTTGACCGGGGT GTCTTGGGTTTTTTGGCTTTCTTGGGCGTGGCTGCCAGCTTCTTCTTGGCCTTCTTGACCGGGGT T A lnc-ANKRD54-1 RNACentral:URS0000D5C511 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr22:37805851..37806100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 112279 RMVar_ID_112279 Human_SNP_ID_844823910 m1A Human chr22 - 42879120 42879118 42879121 GAATCGAACCCTCAGCCGGAGAGAGAAGAAGAAGGCCACTGACGGCGTCACCCTGACGGGCATCA GAATCGAACCCTCAGCCGGAGAGAGAAGAAG___GCCACTGACGGCGTCACCCTGACGGGCATCA CCTT C PACSIN2 Ensembl:ENSG00000100266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr22:42879007..42879179 26863196 MeRIP-seq:(Medium) rs765787751 Functional Loss DEL TCGA 32..34 33 COAD 1 - Human_RBP_ID_9392462,Human_RBP_ID_19112310,Human_RBP_ID_22455060,Human_RBP_ID_25680670 Human_Splice_Rec_2173066,Human_Splice_Rec_2173067,Human_Splice_Rec_2173084,Human_Splice_Rec_2173085,Human_Splice_Rec_2173104,Human_Splice_Rec_2173105,Human_Splice_Rec_2173122,Human_Splice_Rec_2173123,Human_Splice_Rec_2173142,Human_Splice_Rec_2173143,Human_Splice_Rec_2173162,Human_Splice_Rec_2173163 RMVar_hsa_circ_103952,RMVar_hsa_circ_328712,RMVar_hsa_circ_366692,RMVar_hsa_circ_214833,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214832,RMVar_hsa_circ_266424 112280 RMVar_ID_112280 Human_SNP_ID_883363600 m1A Human chrY + 11297768 11297768 11297768 TCTATTTCATGCCATTCCACTCGGGTTGATTCAATTCCATTGTATTCCATTCCATTCCATTCCAT TCTATTTCATGCCATTCCACTCGGGTTGATTCCATTCCATTGTATTCCATTCCATTCCATTCCAT A C RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:11297495..11297842 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 2 - 112281 RMVar_ID_112281 Human_SNP_ID_883468158 m1A Human chrY + 56833302 56833302 56833302 CCATTCCACTCCACTCCATTCCATTCCACTCCATTCCATGCCATTCCATTCCACTCCACTCCATT CCATTCCACTCCACTCCATTCCATTCCACTCCTTTCCATGCCATTCCATTCCACTCCACTCCATT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrY:56833252..56833337 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112282 RMVar_ID_112282 Human_SNP_ID_827872608 m1A Human chr17 - 2303805 2303805 2303805 GCAGGGGGCGGGGAAAGGCCGGGAGGTGGGCGAGCGCGCGCGCCGCCCGTCTGTGGTGGTTTCCT GCAGGGGGCGGGGAAAGGCCGGGAGGTGGGCGCGCGCGCGCGCCGCCCGTCTGTGGTGGTTTCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:2303637..2303810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112283 RMVar_ID_112283 Human_SNP_ID_827881582 m1A Human chr17 - 40928296 40928296 40928296 AGCCACTGTGCAGAGCAGACAAGGTGACATCCACGAACTGAAGCGCACATTCCAGGCCCTGGAGA AGCCACTGTGCAGAGCAGACAAGGTGACATCCTCGAACTGAAGCGCACATTCCAGGCCCTGGAGA T A KRT23 Ensembl:ENSG00000108244 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40921477..40928343 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 2 breast Human_Splice_Rec_1815654,Human_Splice_Rec_1815655,Human_Splice_Rec_1815666,Human_Splice_Rec_1815667,Human_Splice_Rec_1815682,Human_Splice_Rec_1815683,Human_Splice_Rec_1815696,Human_Splice_Rec_1815697,Human_Splice_Rec_1815706 RMVar_hsa_circ_117043,RMVar_hsa_circ_184106 112284 RMVar_ID_112284 Human_SNP_ID_827882588 m1A Human chr17 - 28726052 28726052 28726052 TGCACCCCGCCCTGCCGCTGCTCCTGGGCGCCACGCTGACCTTCCGGGCGCTCCGGCGCGCGCTC TGCACCCCGCCCTGCCGCTGCTCCTGGGCGCCGCGCTGACCTTCCGGGCGCTCCGGCGCGCGCTC T C TLCD1 Ensembl:ENSG00000160606 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:28725951..28726162 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 112285 RMVar_ID_112285 Human_SNP_ID_827890166 m1A Human chr17 - 76072446 76072446 76072446 AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCAGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT AGCAGGTCCCAGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGTGGCAGTGGCGGCGGCGGT T C SRP68 Ensembl:ENSG00000167881 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr17:76072390..76072476 26863410 MeRIP-seq:(Medium) rs1041428323 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_3952989,Human_RBP_ID_4452227,Human_RBP_ID_5115772,Human_RBP_ID_24373311 RMVar_hsa_circ_112529,RMVar_hsa_circ_187157 112286 RMVar_ID_112286 Human_SNP_ID_827893526 m1A Human chr17 + 81935023 81935023 81935023 AGAAGCCCACGCTGCTCAGCAGCTGCTCCATGAGCCTCCCGTCCTCCACCTGGGCGTGCGTGCCT AGAAGCCCACGCTGCTCAGCAGCTGCTCCATGGGCCTCCCGTCCTCCACCTGGGCGTGCGTGCCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81934976..81935025 32194978 MeRIP-seq:(Medium) rs1219327272 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 SKCM,mouth squamous_cell_carcinoma,head_neck squamous_cell_carcinoma 16 head and neck 112287 RMVar_ID_112287 Human_SNP_ID_827897239 m1A Human chr17 + 47973929 47973929 47973929 TTTAGTTCTCGAAATCCCGTCTCTTGCTTTCTAGACATTCACTACTTTCACTGCCTAAGAATCCT TTTAGTTCTCGAAATCCCGTCTCTTGCTTTCTGGACATTCACTACTTTCACTGCCTAAGAATCCT A G AC018521.1,CDK5RAP3 Ensembl:ENSG00000263798,Ensembl:ENSG00000108465 lincRNA,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47973926..47974000 32194978 MeRIP-seq:(Medium) rs763027669 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_3952626,Human_RBP_ID_25294960 RMVar_hsa_circ_5074,RMVar_hsa_circ_77297,RMVar_hsa_circ_185063,RMVar_hsa_circ_357514,RMVar_hsa_circ_39158,RMVar_hsa_circ_72412,RMVar_hsa_circ_114438,RMVar_hsa_circ_121431,RMVar_hsa_circ_79313 112288 RMVar_ID_112288 Human_SNP_ID_827903178 m1A Human chr17 - 8143725 8143725 8143725 CCCGTGCCACCCTCCACCCCCTGGCCCACCCCACCAGCCACTACCCCCTTCCCAGCGGTTGTCCA CCCGTGCCACCCTCCACCCCCTGGCCCACCCCCCCAGCCACTACCCCCTTCCCAGCGGTTGTCCA T G PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8143450..8143900 26863196 MeRIP-seq:(Medium) rs950293870 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,LICA 3 head and neck Human_RBP_ID_503681,Human_RBP_ID_17079478,Human_RBP_ID_18941375 Human_miRNA_ID_272065,Human_miRNA_ID_1418797 112289 RMVar_ID_112289 Human_SNP_ID_827914505 m1A Human chr17 + 80427066 80427060 80427066 GCTGGCGCGCAGTGTGGCCTCCAGGGGGCAGCAGCAGCCCACATACCACAATGGCCCTCGCCCTG GCTGGCGCGCAGTGTGGCCTCCAGGGG______GCAGCCCACATACCACAATGGCCCTCGCCCTG GGCAGCA G ENDOV Ensembl:ENSG00000173818 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80427058..80427185 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 28..33 33 BRCA 1 - Human_RBP_ID_17902442 112290 RMVar_ID_112290 Human_SNP_ID_827916014 m1A Human chr17 + 80353611 80353611 80353611 GGAGGTGGCAGAGGTGGCAGAGGAGGCCATGGAAACAGAAAGTTCTGAGAAGGTGGGAAAGGAAA GGAGGTGGCAGAGGTGGCAGAGGAGGCCATGGCAACAGAAAGTTCTGAGAAGGTGGGAAAGGAAA A C RNF213 Ensembl:ENSG00000173821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:80353560..80353662 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_820357,Human_RBP_ID_897002,Human_RBP_ID_3951260,Human_RBP_ID_5526494,Human_RBP_ID_18989456,Human_RBP_ID_26332520 Human_Splice_Rec_1878514,Human_Splice_Rec_1878515,Human_Splice_Rec_1878646,Human_Splice_Rec_1878647 RMVar_hsa_circ_4887,RMVar_hsa_circ_40321,RMVar_hsa_circ_127968,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_187496,RMVar_hsa_circ_104895,RMVar_hsa_circ_187500,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031,RMVar_hsa_circ_110974,RMVar_hsa_circ_187504,RMVar_hsa_circ_75089,RMVar_hsa_circ_265404,RMVar_hsa_circ_268866,RMVar_hsa_circ_105315,RMVar_hsa_circ_64685,RMVar_hsa_circ_95834,RMVar_hsa_circ_187507,RMVar_hsa_circ_187509,RMVar_hsa_circ_85498,RMVar_hsa_circ_187508,RMVar_hsa_circ_58270,RMVar_hsa_circ_90136,RMVar_hsa_circ_187511,RMVar_hsa_circ_372766,RMVar_hsa_circ_41736,RMVar_hsa_circ_187512 112291 RMVar_ID_112291 Human_SNP_ID_827918530 m1A Human chr17 + 3818475 3818475 3818475 AGCTCCTCGTGGTACTCTACCACCACTCTGTCATCTGCATCCATGTCCTGGTCTTCTTCTTCCTC AGCTCCTCGTGGTACTCTACCACCACTCTGTCGTCTGCATCCATGTCCTGGTCTTCTTCTTCCTC A G lnc-HASPIN-2 RNACentral:URS00008B34B5 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3818424..3818534 26863196 MeRIP-seq:(Medium) rs773526709 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112292 RMVar_ID_112292 Human_SNP_ID_827922908 m1A Human chr17 - 44967992 44967992 44967992 ATCCCCGTGCTGGTGAGCTCGGGCGGCCCGGAAGGCCACTATGAGATGCTGGGCACCTGCCGCAT ATCCCCGTGCTGGTGAGCTCGGGCGGCCCGGACGGCCACTATGAGATGCTGGGCACCTGCCGCAT T G C1QL1 Ensembl:ENSG00000131094 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44967851..44968333 26863196 MeRIP-seq:(Medium) rs1461774723 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4432078 112293 RMVar_ID_112293 Human_SNP_ID_827934256 m1A Human chr17 + 7573218 7573218 7573218 GCGGCCGCCACTATGTGTGGCCCAGAGCCGGCAGGTCCGGTTGCCTCCCTGTGCCGGGGGAGGGA GCGGCCGCCACTATGTGTGGCCCAGAGCCGGCCGGTCCGGTTGCCTCCCTGTGCCGGGGGAGGGA A C SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7573216..7573525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_3545030,Human_RBP_ID_5648411,Human_RBP_ID_8190895,Human_RBP_ID_17126575,Human_RBP_ID_18486336,Human_RBP_ID_22715940,Human_RBP_ID_26781541 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885 112294 RMVar_ID_112294 Human_SNP_ID_827944212 m1A Human chr17 - 28749333 28749333 28749333 GTTTAGCCAGCCCAGGGTCGCTCTGATCCAGCAGGGAGAAGGTGACACGGCGGGCAAAGGGCCAC GTTTAGCCAGCCCAGGGTCGCTCTGATCCAGCTGGGAGAAGGTGACACGGCGGGCAAAGGGCCAC T A RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:28749284..28749443 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma 4 kidney 112295 RMVar_ID_112295 Human_SNP_ID_827945527 m1A Human chr17 + 51161271 51161271 51161271 CCATCCGTGGAGACTTCTGCATACAAGTTGGCAGGTGAGATTTTGGTATTTTTCCCCCTTTTCCA CCATCCGTGGAGACTTCTGCATACAAGTTGGCGGGTGAGATTTTGGTATTTTTCCCCCTTTTCCA A G NME1-NME2,NME1 Ensembl:ENSG00000011052,Ensembl:ENSG00000239672 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:51161116..51161311 26863196 MeRIP-seq:(Medium) rs763630436 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 8 stomach Human_RBP_ID_5115210,Human_RBP_ID_22760854 Human_Splice_Rec_1842259,Human_Splice_Rec_1842271,Human_Splice_Rec_1842299,Human_Splice_Rec_1842309,Human_Splice_Rec_1842321,Human_Splice_Rec_1842335,Human_Splice_Rec_1842349 Human_miRNA_ID_1478388,Human_miRNA_ID_1478389 RMVar_hsa_circ_119324,RMVar_hsa_circ_78484,RMVar_hsa_circ_110250,RMVar_hsa_circ_185439,RMVar_hsa_circ_185440,RMVar_hsa_circ_185441,RMVar_hsa_circ_85778,RMVar_hsa_circ_25513,RMVar_hsa_circ_39095,RMVar_hsa_circ_114119,RMVar_hsa_circ_51912,RMVar_hsa_circ_185443,RMVar_hsa_circ_185444,RMVar_hsa_circ_91843,RMVar_hsa_circ_314766,RMVar_hsa_circ_185445 112296 RMVar_ID_112296 Human_SNP_ID_827948014 m1A Human chr17 + 18247356 18247356 18247356 CATCGTCCCAATTCTTGAACTTGGCCTTGAACACCTGCCAGGGAGGCCATCAACTAACCATGAGG CATCGTCCCAATTCTTGAACTTGGCCTTGAACGCCTGCCAGGGAGGCCATCAACTAACCATGAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18247326..18247375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 112297 RMVar_ID_112297 Human_SNP_ID_827948293 m1A Human chr17 - 8629636 8629636 8629636 CTGCAGTTGGGGGTCACACCCTGATCCCATAAAATCGGACTGGAATTGGTTCGGAGGGAAGTTGA CTGCAGTTGGGGGTCACACCCTGATCCCATAATATCGGACTGGAATTGGTTCGGAGGGAAGTTGA T A MYH10 Ensembl:ENSG00000133026 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:8629630..8629888 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8467764 RMVar_hsa_circ_115357,RMVar_hsa_circ_182045 112298 RMVar_ID_112298 Human_SNP_ID_827951878 m1A Human chr17 - 15487617 15487617 15487617 GCAAAGATTTGCGTCTGTAGTGTGCATGTTTGAGGCACAACAAGGAGGCTACAGTGGCTGGGGCA GCAAAGATTTGCGTCTGTAGTGTGCATGTTTGCGGCACAACAAGGAGGCTACAGTGGCTGGGGCA T G TVP23C-CDRT4,CDRT4 Ensembl:ENSG00000259024,Ensembl:ENSG00000239704 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:15487566..15487716 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 112299 RMVar_ID_112299 Human_SNP_ID_827953687 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCCAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,brain astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III,oesophagus squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,penis squamous_cell_carcinoma,ESCA,large_intestine adenocarcinoma 115 oesophagus,penis,stomach,large intestine,haematopoietic and lymphoid tissue,brain Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 112300 RMVar_ID_112300 Human_SNP_ID_827953691 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCGAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 colon adenocarcinoma,mouth squamous_cell_carcinoma,lung adenocarcinoma,oesophagus squamous_cell_carcinoma,UCEC,ESCA,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_B_cell_leukaemia,ovary serous_carcinoma,urinary_tract transitional_cell_carcinoma,BRCA,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,haematopoietic_and_lymphoid_tissue essential_thrombocythaemia,SARC,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,head_neck squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue follicular_lymphoma,CHOL,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,bladder transitional_cell_carcinoma 309 lung,biliary tract,ovary,gallbladder,oesophagus,bladder,urinary tract,head and neck,large intestine,haematopoietic and lymphoid tissue Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 112301 RMVar_ID_112301 Human_SNP_ID_827953703 m1A Human chr17 + 7675209 7675209 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCTAAACATCTTGTTGAGGGCAGGGGAGTACTGTA A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) rs1057519975 Functional Loss SNV COSMIC 33..33 33 lymph_node B_cell_lymphoma_unspecified,brain astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia,haematopoietic_and_lymphoid_tissue B_cell_lymphoma_unspecified 95 brain,haematopoietic and lymphoid tissue Clinvar_Rec_658,Clinvar_Rec_659,Clinvar_Rec_660 GWAS_ID_13673,GWAS_ID_13674,GWAS_ID_13675,GWAS_ID_13676,GWAS_ID_13677,GWAS_ID_13678,GWAS_ID_13679,GWAS_ID_13680,GWAS_ID_13681,GWAS_ID_13682,GWAS_ID_13683,GWAS_ID_13684,GWAS_ID_13685,GWAS_ID_13686,GWAS_ID_13687,GWAS_ID_13688,GWAS_ID_13689,GWAS_ID_13690,GWAS_ID_13691,GWAS_ID_13692,GWAS_ID_13693 112302 RMVar_ID_112302 Human_SNP_ID_827955841 m1A Human chr17 - 72891529 72891529 72891529 ACTGAGGGGAGAGAGTGAGGATAGAACCTTCCAGACTGGGGAGCAGCAAGTGGGAGGCTATGAGG ACTGAGGGGAGAGAGTGAGGATAGAACCTTCCGGACTGGGGAGCAGCAAGTGGGAGGCTATGAGG T C SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:72891528..72891631 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_110240,RMVar_hsa_circ_343678,RMVar_hsa_circ_186867 112303 RMVar_ID_112303 Human_SNP_ID_827955910 m1A Human chr17 - 72647540 72647540 72647540 TTCGGACCCCGGGAAAGGCCATACGAAGAAACAGCAGTGGTTGGCTTCTATGGGACAACAAGCTT TTCGGACCCCGGGAAAGGCCATACGAAGAAACGGCAGTGGTTGGCTTCTATGGGACAACAAGCTT T C SLC39A11 Ensembl:ENSG00000133195 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:72647443..72648833 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_498687,Human_RBP_ID_8462073 RMVar_hsa_circ_78310,RMVar_hsa_circ_107514,RMVar_hsa_circ_186862,RMVar_hsa_circ_186863 112304 RMVar_ID_112304 Human_SNP_ID_827961211 m1A Human chr17 - 16536159 16536159 16536159 TGGCCCACCATTGGCCACCCTATTCATTATTAACTGAGACTCGTAACTGCACCCCAGCTCGACTT TGGCCCACCATTGGCCACCCTATTCATTATTAGCTGAGACTCGTAACTGCACCCCAGCTCGACTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16536109..16536174 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112305 RMVar_ID_112305 Human_SNP_ID_827961308 m1A Human chr17 + 38898496 38898496 38898496 TGGCAGACACGCCCGAGCTCCAGAGAATCAAGAAGACCCAGGACCAGATCAGTAACGTGAGCTCT TGGCAGACACGCCCGAGCTCCAGAGAATCAAGGAGACCCAGGACCAGATCAGTAACGTGAGCTCT A G LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:38898364..38898575;chr17:38898401..38898563;chr17:38898359..38898577 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_904690,Human_RBP_ID_5577189,Human_RBP_ID_9375804,Human_RBP_ID_19078913,Human_RBP_ID_24552284,Human_RBP_ID_26330713 Human_Splice_Rec_1810238,Human_Splice_Rec_1810239,Human_Splice_Rec_1810248,Human_Splice_Rec_1810249,Human_Splice_Rec_1810260,Human_Splice_Rec_1810261,Human_Splice_Rec_1810272,Human_Splice_Rec_1810279,Human_Splice_Rec_1810290,Human_Splice_Rec_1810291,Human_Splice_Rec_1810302,Human_Splice_Rec_1810303,Human_Splice_Rec_1810308,Human_Splice_Rec_1810309 Human_miRNA_ID_254203,Human_miRNA_ID_2041114,Human_miRNA_ID_2157982,Human_miRNA_ID_3020097 RMVar_hsa_circ_47170,RMVar_hsa_circ_316168,RMVar_hsa_circ_127058,RMVar_hsa_circ_322945,RMVar_hsa_circ_183848,RMVar_hsa_circ_183850,RMVar_hsa_circ_183852,RMVar_hsa_circ_115523,RMVar_hsa_circ_183851 112306 RMVar_ID_112306 Human_SNP_ID_827967293 m1A Human chr17 + 77488289 77488289 77488289 GTCCGGATGAAGCTGACAGTGATTGACACACCAGGGTTCGGGGACCACATCAACAACGAGAACTG GTCCGGATGAAGCTGACAGTGATTGACACACCTGGGTTCGGGGACCACATCAACAACGAGAACTG A T SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:77488197..77488371 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 16 ovary Human_RBP_ID_49510,Human_RBP_ID_6647425,Human_RBP_ID_8822756,Human_RBP_ID_9376929,Human_RBP_ID_17262153,Human_RBP_ID_17494240,Human_RBP_ID_17901658,Human_RBP_ID_26812804 Human_Splice_Rec_1873366,Human_Splice_Rec_1873367,Human_Splice_Rec_1873388,Human_Splice_Rec_1873389,Human_Splice_Rec_1873414,Human_Splice_Rec_1873415,Human_Splice_Rec_1873436,Human_Splice_Rec_1873437,Human_Splice_Rec_1873462,Human_Splice_Rec_1873463,Human_Splice_Rec_1873482,Human_Splice_Rec_1873483,Human_Splice_Rec_1873502,Human_Splice_Rec_1873503,Human_Splice_Rec_1873518,Human_Splice_Rec_1873519,Human_Splice_Rec_1873542,Human_Splice_Rec_1873543,Human_Splice_Rec_1873574,Human_Splice_Rec_1873575,Human_Splice_Rec_1873600,Human_Splice_Rec_1873601,Human_Splice_Rec_1873618,Human_Splice_Rec_1873619,Human_Splice_Rec_1873626,Human_Splice_Rec_1873632,Human_Splice_Rec_1873633,Human_Splice_Rec_1873644,Human_Splice_Rec_1873650,Human_Splice_Rec_1873651,Human_Splice_Rec_1873668,Human_Splice_Rec_1873669,Human_Splice_Rec_1873678,Human_Splice_Rec_1873679,Human_Splice_Rec_1873694,Human_Splice_Rec_1873695,Human_Splice_Rec_1873712,Human_Splice_Rec_1873713,Human_Splice_Rec_1873720,Human_Splice_Rec_1873721,Human_Splice_Rec_1873738,Human_Splice_Rec_1873739,Human_Splice_Rec_1873746,Human_Splice_Rec_1873747,Human_Splice_Rec_1873758,Human_Splice_Rec_1873759,Human_Splice_Rec_1873766,Human_Splice_Rec_1873767,Human_Splice_Rec_1873776,Human_Splice_Rec_1873777,Human_Splice_Rec_1873792,Human_Splice_Rec_1873796,Human_Splice_Rec_1873797 RMVar_hsa_circ_72557,RMVar_hsa_circ_66421,RMVar_hsa_circ_314705,RMVar_hsa_circ_187290 112307 RMVar_ID_112307 Human_SNP_ID_827967389 m1A Human chr17 + 79937406 79937406 79937406 CAGCATCTTCATCTTGTCCTGATGCCCTGCCCACCCCCGCCGAGCTTCACACTGGGCTGCTATGG CAGCATCTTCATCTTGTCCTGATGCCCTGCCCCCCCCCGCCGAGCTTCACACTGGGCTGCTATGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79937363..79937481 26863196 MeRIP-seq:(Medium) rs1021297187 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112308 RMVar_ID_112308 Human_SNP_ID_827967600 m1A Human chr17 - 82025544 82025544 82025544 CACCCCGCCCTCGGTGGACAGGCCTCTGTCAAAGGCTCACGCGTCACTCCACACAGCCCTGCACC CACCCCGCCCTCGGTGGACAGGCCTCTGTCAAGGGCTCACGCGTCACTCCACACAGCCCTGCACC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82025528..82025612 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112309 RMVar_ID_112309 Human_SNP_ID_827972999 m1A Human chr17 + 67826152 67826150 67826153 GGAGGAGGAGGAAGAGGAGGACATGGTCTCCGAGGAGGAGGAGGAGGAGGACGGCGACGCCGAGG GGAGGAGGAGGAAGAGGAGGACATGGTCTCC___GAGGAGGAGGAGGAGGACGGCGACGCCGAGG CGAG C BPTF Ensembl:ENSG00000171634 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:67826072..67826248 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 LICA 1 - Human_RBP_ID_6638446,Human_RBP_ID_9289340,Human_RBP_ID_22959270,Human_RBP_ID_23118787,Human_RBP_ID_24371849 112310 RMVar_ID_112310 Human_SNP_ID_827976060 m1A Human chr17 + 57974576 57974576 57974576 TGAGAGGGGCGGCTAATGTCATAGGTGTGGGTAGATTCATTGGAGATGTGATGGTGACAGGGTGT TGAGAGGGGCGGCTAATGTCATAGGTGTGGGTTGATTCATTGGAGATGTGATGGTGACAGGGTGT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57974526..57974700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine 112311 RMVar_ID_112311 Human_SNP_ID_827977891 m1A Human chr17 + 75521788 75521788 75521788 TCTGGCAGCCTCCAGCCCACCTCCCTGCAGCCAGCCCAGCCAATGCCCAGAGGAGAAACCCCAGG TCTGGCAGCCTCCAGCCCACCTCCCTGCAGCCGGCCCAGCCAATGCCCAGAGGAGAAACCCCAGG A G TSEN54 Ensembl:ENSG00000182173 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:75521737..75521981 26863196 MeRIP-seq:(Medium) rs200904080 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_499856,Human_RBP_ID_900724,Human_RBP_ID_17900791 Human_Splice_Rec_1866442,Human_Splice_Rec_1866486,Human_Splice_Rec_1866496 Human_miRNA_ID_794143,Human_miRNA_ID_935711,Human_miRNA_ID_1158036,Human_miRNA_ID_2333065,Human_miRNA_ID_2435106,Human_miRNA_ID_2555008,Human_miRNA_ID_2966147 RMVar_hsa_circ_116486,RMVar_hsa_circ_187042 112312 RMVar_ID_112312 Human_SNP_ID_827980464 m1A Human chr17 + 7687427 7687374 7687427 TCACCGTCGTGGAAAGCACGCTCCCAGCCCGAACGCAAAGTGTCCCCGGAGCCCAGCAGCTACCT _________________________________CGCAAAGTGTCCCCGGAGCCCAGCAGCTACCT TACCCAATCCAGGGAAGCGTGTCACCGTCGTGGAAAGCACGCTCCCAGCCCGAA T WRAP53 Ensembl:ENSG00000141499 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7687110..7687475 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 1..33 33 OV 1 - 112313 RMVar_ID_112313 Human_SNP_ID_827980606 m1A Human chr17 - 48607815 48607815 48607815 GAGTGAGGGATGGAGAAAGGGCAGAGGAAGAGACATGAGAAAGGGAGAGGAAGAGAAGCCCAGCT GAGTGAGGGATGGAGAAAGGGCAGAGGAAGAGGCATGAGAAAGGGAGAGGAAGAGAAGCCCAGCT T C HOXB7 Ensembl:ENSG00000260027 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:48607764..48607999 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_4474937 112314 RMVar_ID_112314 Human_SNP_ID_827984846 m1A Human chr17 + 50077424 50077424 50077424 AAGCTAATGAGACCATCTTTTGCGAGCTGGGGAACCCCTTCAAACGGAACCAGAGGGTGAGCACC AAGCTAATGAGACCATCTTTTGCGAGCTGGGGGACCCCTTCAAACGGAACCAGAGGGTGAGCACC A G ITGA3 Ensembl:ENSG00000005884 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50077376..50077425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver combined_hepatocellular-cholangiocarcinoma 2 liver Human_Splice_Rec_1836893,Human_Splice_Rec_1836942,Human_Splice_Rec_1836943,Human_Splice_Rec_1836992,Human_Splice_Rec_1836993,Human_Splice_Rec_1837040,Human_Splice_Rec_1837041,Human_Splice_Rec_1837049 Human_miRNA_ID_869307,Human_miRNA_ID_2258314,Human_miRNA_ID_2385697 RMVar_hsa_circ_22567,RMVar_hsa_circ_185186,RMVar_hsa_circ_89683,RMVar_hsa_circ_375206,RMVar_hsa_circ_185191,RMVar_hsa_circ_121818,RMVar_hsa_circ_124085,RMVar_hsa_circ_185196,RMVar_hsa_circ_114628,RMVar_hsa_circ_78770,RMVar_hsa_circ_78895,RMVar_hsa_circ_185198,RMVar_hsa_circ_185199,RMVar_hsa_circ_115593,RMVar_hsa_circ_86401,RMVar_hsa_circ_120952,RMVar_hsa_circ_185200,RMVar_hsa_circ_185201,RMVar_hsa_circ_185203,RMVar_hsa_circ_185204,RMVar_hsa_circ_185207,RMVar_hsa_circ_371089,RMVar_hsa_circ_372802,RMVar_hsa_circ_84842,RMVar_hsa_circ_94524,RMVar_hsa_circ_127843,RMVar_hsa_circ_185213,RMVar_hsa_circ_185214,RMVar_hsa_circ_185215,RMVar_hsa_circ_185212,RMVar_hsa_circ_185217,RMVar_hsa_circ_80768,RMVar_hsa_circ_339193,RMVar_hsa_circ_185216,RMVar_hsa_circ_185221,RMVar_hsa_circ_106065,RMVar_hsa_circ_115154,RMVar_hsa_circ_185223,RMVar_hsa_circ_88721,RMVar_hsa_circ_185222,RMVar_hsa_circ_185220,RMVar_hsa_circ_122182,RMVar_hsa_circ_120554,RMVar_hsa_circ_100198,RMVar_hsa_circ_185226,RMVar_hsa_circ_185227,RMVar_hsa_circ_2486,RMVar_hsa_circ_108684,RMVar_hsa_circ_82116,RMVar_hsa_circ_185228,RMVar_hsa_circ_185229,RMVar_hsa_circ_91822,RMVar_hsa_circ_23890,RMVar_hsa_circ_185230,RMVar_hsa_circ_185231 112315 RMVar_ID_112315 Human_SNP_ID_827987972 m1A Human chr17 - 42963583 42963583 42963583 AAGATGTTCCTGAAGGAGTTCAGGTGAGATAGACGGGTTACAGTAGTACAGCAGAGAGCATATTT AAGATGTTCCTGAAGGAGTTCAGGTGAGATAGCCGGGTTACAGTAGTACAGCAGAGAGCATATTT T G AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42963578..42963709 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_13012883 RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_184514,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 112316 RMVar_ID_112316 Human_SNP_ID_827996973 m1A Human chr17 - 32350226 32350226 32350226 GGAGGAGAAAAGAAGCAGGAGAAACGAGGCCAAAAATCCCTCACTTTCCCAACCCAACGGCTACC GGAGGAGAAAAGAAGCAGGAGAAACGAGGCCACAAATCCCTCACTTTCCCAACCCAACGGCTACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:32350176..32350413 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112317 RMVar_ID_112317 Human_SNP_ID_828000878 m1A Human chr17 + 7944638 7944638 7944638 CTCAGCACCACTCTCCCGCCGCCCAACCCTCCAGTACGCCTTACCCCTTGAGCTAAGCTTCTCCG CTCAGCACCACTCTCCCGCCGCCCAACCCTCCCGTACGCCTTACCCCTTGAGCTAAGCTTCTCCG A C CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7944469..7945362 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_Splice_Rec_1775489,Human_Splice_Rec_1775525,Human_Splice_Rec_1775579,Human_Splice_Rec_1775643,Human_Splice_Rec_1775661 RMVar_hsa_circ_9763,RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_54922,RMVar_hsa_circ_356758,RMVar_hsa_circ_181985,RMVar_hsa_circ_344070,RMVar_hsa_circ_86347,RMVar_hsa_circ_111803,RMVar_hsa_circ_181986,RMVar_hsa_circ_377147,RMVar_hsa_circ_181987 112318 RMVar_ID_112318 Human_SNP_ID_828001278 m1A Human chr17 - 35809573 35809573 35809573 TGCCGCTGCTCGCTGAAGAAGTCACCTACCCGACATGACTAACGGCCGCGGCGCGGAGGCCCCAC TGCCGCTGCTCGCTGAAGAAGTCACCTACCCGGCATGACTAACGGCCGCGGCGCGGAGGCCCCAC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:35809451..35809638 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - 112319 RMVar_ID_112319 Human_SNP_ID_828005638 m1A Human chr17 - 43778884 43778884 43778884 CTCGTTCGAGCTCTCGGTGCAGGATCTCAACGACCTGCTCTCGGACGGCAGCGGCTGCTACAGCC CTCGTTCGAGCTCTCGGTGCAGGATCTCAACGGCCTGCTCTCGGACGGCAGCGGCTGCTACAGCC T C DUSP3 Ensembl:ENSG00000108861 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:43778848..43778936 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_1534739,Human_RBP_ID_4465442,Human_RBP_ID_5420110,Human_RBP_ID_5441480,Human_RBP_ID_18439056 Human_Splice_Rec_1823863,Human_Splice_Rec_1823875 112320 RMVar_ID_112320 Human_SNP_ID_828008968 m1A Human chr17 - 82078652 82078652 82078652 GCTGCGGCCCCCTCTCGGCCAGGCATTGGCTCAGCCCGCTGAGTGGGGGGTCGTGGGCCAGTCCC GCTGCGGCCCCCTCTCGGCCAGGCATTGGCTCGGCCCGCTGAGTGGGGGGTCGTGGGCCAGTCCC T C FASN Ensembl:ENSG00000169710 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82078601..82078973 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_503422,Human_RBP_ID_4461055,Human_RBP_ID_5114986,Human_RBP_ID_5143412,Human_RBP_ID_22061840,Human_RBP_ID_26460093 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 112321 RMVar_ID_112321 Human_SNP_ID_828009098 m1A Human chr17 - 56904453 56904453 56904453 ACTGCAAACAGAAAGGTGGAGCAGCTACAACAAGAATACACGGAAATGAAGGCTCTCTTGGACGC ACTGCAAACAGAAAGGTGGAGCAGCTACAACACGAATACACGGAAATGAAGGCTCTCTTGGACGC T G TRIM25 Ensembl:ENSG00000121060 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:56904376..56904534 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_47728,Human_RBP_ID_2513724,Human_RBP_ID_6616828,Human_RBP_ID_18530773,Human_RBP_ID_26333630 Human_Splice_Rec_1843822,Human_Splice_Rec_1843846,Human_Splice_Rec_1843864,Human_Splice_Rec_1843882,Human_Splice_Rec_1843912 Human_miRNA_ID_2196086,Human_miRNA_ID_2196087 RMVar_hsa_circ_122008,RMVar_hsa_circ_53718,RMVar_hsa_circ_185565,RMVar_hsa_circ_78975,RMVar_hsa_circ_349395,RMVar_hsa_circ_366682,RMVar_hsa_circ_185564,RMVar_hsa_circ_127581,RMVar_hsa_circ_57800,RMVar_hsa_circ_53597,RMVar_hsa_circ_185572,RMVar_hsa_circ_185571,RMVar_hsa_circ_299913,RMVar_hsa_circ_73823,RMVar_hsa_circ_366553 112322 RMVar_ID_112322 Human_SNP_ID_828010825 m1A Human chr17 - 47975640 47975640 47975640 GAAGCTGAGGCCTCTCTACCTCTCACACACAAACCCCACAGACGCCTGGTACACGTCAATGGCTT GAAGCTGAGGCCTCTCTACCTCTCACACACAAGCCCCACAGACGCCTGGTACACGTCAATGGCTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47975589..47975697 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary 112323 RMVar_ID_112323 Human_SNP_ID_828012141 m1A Human chr17 - 39653631 39653631 39653631 CCTTCGCTTCTCAGGCGGCGGAAGGAGGTGCGAGGAGAGGCTCTGGCTGTGGGACAGTGAGGAGC CCTTCGCTTCTCAGGCGGCGGAAGGAGGTGCGGGGAGAGGCTCTGGCTGTGGGACAGTGAGGAGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39653483..39653633 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 112324 RMVar_ID_112324 Human_SNP_ID_828017751 m1A Human chr17 + 76680769 76680769 76680769 AGCAGATTTATGGAGGCAGCATGCACCCTGGGAGCCTGCCCAGACTCCTCTCTGGGGTTTCCGTT AGCAGATTTATGGAGGCAGCATGCACCCTGGGCGCCTGCCCAGACTCCTCTCTGGGGTTTCCGTT A C SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76680726..76680850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 biliary_tract adenocarcinoma,gallbladder adenocarcinoma 6 biliary tract,gallbladder Human_RBP_ID_18709459 112325 RMVar_ID_112325 Human_SNP_ID_828019707 m1A Human chr17 + 40177426 40177426 40177426 CGGGGGCGAGCCGAGGAAGGGTAGGGGCGGGGACTGGGCGGGGACTGGAGGAGGGGGCGCGGTCT CGGGGGCGAGCCGAGGAAGGGTAGGGGCGGGGGCTGGGCGGGGACTGGAGGAGGGGGCGCGGTCT A G RAPGEFL1 Ensembl:ENSG00000108352 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:40177391..40177556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_22716537 112326 RMVar_ID_112326 Human_SNP_ID_828021415 m1A Human chr17 - 30824548 30824548 30824548 GAGCTACCGGCGGGAGCTGGGTCACCGGCTTGAGGGGCTGCGTGAGGCGCGGAGGCAGGTCGGAG GAGCTACCGGCGGGAGCTGGGTCACCGGCTTGGGGGGCTGCGTGAGGCGCGGAGGCAGGTCGGAG T C CRLF3 Ensembl:ENSG00000176390 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30824526..30824681 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_4465273,Human_RBP_ID_18419572,Human_RBP_ID_23719838 Human_Splice_Rec_1800779,Human_Splice_Rec_1800791 RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 112327 RMVar_ID_112327 Human_SNP_ID_828022328 m1A Human chr17 - 64502479 64502479 64502479 AGAATAAAACCATTGTTTTTGTGGAAACCAAAAGAAGATGTGATGAGCTTACCAGAAAAATGAGG AGAATAAAACCATTGTTTTTGTGGAAACCAAAGGAAGATGTGATGAGCTTACCAGAAAAATGAGG T C DDX5 Ensembl:ENSG00000108654 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_47427,Human_RBP_ID_904047,Human_RBP_ID_1540197,Human_RBP_ID_1867001,Human_RBP_ID_2519315,Human_RBP_ID_3534232,Human_RBP_ID_4445577,Human_RBP_ID_6633545,Human_RBP_ID_8253623,Human_RBP_ID_9289333,Human_RBP_ID_9376627,Human_RBP_ID_9876239,Human_RBP_ID_13130697,Human_RBP_ID_17493299,Human_RBP_ID_18706135,Human_RBP_ID_18992012,Human_RBP_ID_22219282,Human_RBP_ID_22806289,Human_RBP_ID_22956066,Human_RBP_ID_23743522,Human_RBP_ID_24545049,Human_RBP_ID_26332240,Human_RBP_ID_26968870,Human_RBP_ID_27813017 Human_Splice_Rec_1855054,Human_Splice_Rec_1855055,Human_Splice_Rec_1855076,Human_Splice_Rec_1855077,Human_Splice_Rec_1855098,Human_Splice_Rec_1855099,Human_Splice_Rec_1855122,Human_Splice_Rec_1855123,Human_Splice_Rec_1855142,Human_Splice_Rec_1855143,Human_Splice_Rec_1855166,Human_Splice_Rec_1855167,Human_Splice_Rec_1855192,Human_Splice_Rec_1855193,Human_Splice_Rec_1855202,Human_Splice_Rec_1855212 Human_miRNA_ID_216810 RMVar_hsa_circ_13328,RMVar_hsa_circ_59606,RMVar_hsa_circ_60060,RMVar_hsa_circ_108312,RMVar_hsa_circ_320284,RMVar_hsa_circ_291366,RMVar_hsa_circ_97178,RMVar_hsa_circ_93625,RMVar_hsa_circ_113919,RMVar_hsa_circ_186434,RMVar_hsa_circ_186435,RMVar_hsa_circ_186433,RMVar_hsa_circ_186437,RMVar_hsa_circ_82355,RMVar_hsa_circ_186436,RMVar_hsa_circ_186439,RMVar_hsa_circ_362799,RMVar_hsa_circ_186438,RMVar_hsa_circ_363186,RMVar_hsa_circ_326221 112328 RMVar_ID_112328 Human_SNP_ID_828026535 m1A Human chr17 + 82446569 82446569 82446569 GCCCTTCCTCCTCCTTTCATTCCCATTGCAAAAAACCCAGGAGCTGAACAGCCCTGGACTCTGTC GCCCTTCCTCCTCCTTTCATTCCCATTGCAAACAACCCAGGAGCTGAACAGCCCTGGACTCTGTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82446567..82446689 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112329 RMVar_ID_112329 Human_SNP_ID_828032459 m1A Human chr17 - 49413233 49413233 49413233 CATGGCTGCCAAAGTGTTTGAGTCCATTGGCAAGTTTGGCCTGGCCTTAGCTGTTGCAGGAGGCG CATGGCTGCCAAAGTGTTTGAGTCCATTGGCAGGTTTGGCCTGGCCTTAGCTGTTGCAGGAGGCG T C PHB Ensembl:ENSG00000167085 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49413176..49414756 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_492984,Human_RBP_ID_1536533,Human_RBP_ID_3527395,Human_RBP_ID_4466564,Human_RBP_ID_5115556,Human_RBP_ID_5364541,Human_RBP_ID_9376318,Human_RBP_ID_17654261,Human_RBP_ID_17904984,Human_RBP_ID_22444746,Human_RBP_ID_23210030,Human_RBP_ID_23733250 Human_Splice_Rec_1835730,Human_Splice_Rec_1835731,Human_Splice_Rec_1835744,Human_Splice_Rec_1835745,Human_Splice_Rec_1835756,Human_Splice_Rec_1835757,Human_Splice_Rec_1835764,Human_Splice_Rec_1835765,Human_Splice_Rec_1835780,Human_Splice_Rec_1835781,Human_Splice_Rec_1835792,Human_Splice_Rec_1835793,Human_Splice_Rec_1835803,Human_Splice_Rec_1835811,Human_Splice_Rec_1835820,Human_Splice_Rec_1835821,Human_Splice_Rec_1835830,Human_Splice_Rec_1835831,Human_Splice_Rec_1835844,Human_Splice_Rec_1835845,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 112330 RMVar_ID_112330 Human_SNP_ID_828032961 m1A Human chr17 + 17126781 17126781 17126781 TGTGGTGGATGGGGAGGGCCGCACGGGCCAGAAGTTCTCCCTGTGTATTCTGACGCCTGAGAAGG TGTGGTGGATGGGGAGGGCCGCACGGGCCAGAGGTTCTCCCTGTGTATTCTGACGCCTGAGAAGG A G MPRIP Ensembl:ENSG00000133030 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17126751..17126842 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_1849957,Human_RBP_ID_8445352,Human_RBP_ID_8813599,Human_RBP_ID_21890449 Human_Splice_Rec_1784982,Human_Splice_Rec_1784988,Human_Splice_Rec_1784989,Human_Splice_Rec_1785042,Human_Splice_Rec_1785043,Human_Splice_Rec_1785086,Human_Splice_Rec_1785087 Human_miRNA_ID_2073042,Human_miRNA_ID_2074723,Human_miRNA_ID_3064884 RMVar_hsa_circ_76119,RMVar_hsa_circ_102997,RMVar_hsa_circ_118635,RMVar_hsa_circ_127754,RMVar_hsa_circ_120050,RMVar_hsa_circ_103932,RMVar_hsa_circ_108633,RMVar_hsa_circ_103498,RMVar_hsa_circ_92104,RMVar_hsa_circ_99928,RMVar_hsa_circ_101023,RMVar_hsa_circ_99099,RMVar_hsa_circ_85121,RMVar_hsa_circ_86770,RMVar_hsa_circ_76301,RMVar_hsa_circ_182346,RMVar_hsa_circ_182350,RMVar_hsa_circ_182354,RMVar_hsa_circ_182356,RMVar_hsa_circ_182357,RMVar_hsa_circ_182355,RMVar_hsa_circ_182352,RMVar_hsa_circ_182353,RMVar_hsa_circ_182351,RMVar_hsa_circ_182348,RMVar_hsa_circ_182349,RMVar_hsa_circ_182347,RMVar_hsa_circ_118056,RMVar_hsa_circ_182344,RMVar_hsa_circ_182345,RMVar_hsa_circ_182343,RMVar_hsa_circ_182360,RMVar_hsa_circ_81406,RMVar_hsa_circ_82985,RMVar_hsa_circ_182361,RMVar_hsa_circ_100905,RMVar_hsa_circ_182359,RMVar_hsa_circ_182365,RMVar_hsa_circ_84479,RMVar_hsa_circ_182364 112331 RMVar_ID_112331 Human_SNP_ID_828033057 m1A Human chr17 + 4893575 4893575 4893575 AGGAGGAAGGCGAAGGCGGGCCAGCAGAGGGGAGCAGAGATACCCCTGGGGGCCGGTACGGCATC AGGAGGAAGGCGAAGGCGGGCCAGCAGAGGGGCGCAGAGATACCCCTGGGGGCCGGTACGGCATC A C MINK1 Ensembl:ENSG00000141503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4893453..4893617 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_3949960,Human_RBP_ID_5467349,Human_RBP_ID_18987686,Human_RBP_ID_23114444 Human_Splice_Rec_1764761,Human_Splice_Rec_1764821,Human_Splice_Rec_1764883,Human_Splice_Rec_1764945,Human_Splice_Rec_1765007,Human_Splice_Rec_1765105 RMVar_hsa_circ_181523,RMVar_hsa_circ_111006,RMVar_hsa_circ_98539,RMVar_hsa_circ_100463,RMVar_hsa_circ_181525,RMVar_hsa_circ_181529 112332 RMVar_ID_112332 Human_SNP_ID_828036287 m1A Human chr17 - 28881892 28881892 28881892 TGCCGTGGAGGCACAGGAGATCCTGCGTACGGACAAGGAGCTCATCGCTACAGTGCGCCGGCCTG TGCCGTGGAGGCACAGGAGATCCTGCGTACGGCCAAGGAGCTCATCGCTACAGTGCGCCGGCCTG T G FLOT2 Ensembl:ENSG00000132589 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28881842..28882025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_4414895,Human_RBP_ID_9289980,Human_RBP_ID_9340983,Human_RBP_ID_17888166,Human_RBP_ID_18191204 Human_Splice_Rec_1797475,Human_Splice_Rec_1797497,Human_Splice_Rec_1797517,Human_Splice_Rec_1797537,Human_Splice_Rec_1797557,Human_Splice_Rec_1797573,Human_Splice_Rec_1797589 Human_miRNA_ID_2894643 RMVar_hsa_circ_3287,RMVar_hsa_circ_120844,RMVar_hsa_circ_125372,RMVar_hsa_circ_108294,RMVar_hsa_circ_183033,RMVar_hsa_circ_77536,RMVar_hsa_circ_84791,RMVar_hsa_circ_183035,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032,RMVar_hsa_circ_313669,RMVar_hsa_circ_183039,RMVar_hsa_circ_79161 112333 RMVar_ID_112333 Human_SNP_ID_828053657 m1A Human chr17 + 35001975 35001975 35001975 TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCACTACAGGGGGTAGCAGTGAAGAGAATAAGGGT TCACTGTAGTGGCTGGAGATGAGGGGAGCTCCGCTACAGGGGGTAGCAGTGAAGAGAATAAGGGT A G LIG3 Ensembl:ENSG00000005156 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:35001933..35002053 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary Human_RBP_ID_17691769,Human_RBP_ID_17904789,Human_RBP_ID_27812550 Human_Splice_Rec_1804178,Human_Splice_Rec_1804216,Human_Splice_Rec_1804290 RMVar_hsa_circ_92027,RMVar_hsa_circ_115,RMVar_hsa_circ_183623,RMVar_hsa_circ_358905 112334 RMVar_ID_112334 Human_SNP_ID_828055069 m1A Human chr17 - 44932244 44932244 44932244 CATCCTGCCTCTCAAACCCTCCTTTCCCGCTTAGCCTTCCCAGCTCCCCCTTGCCACCCCACCCT CATCCTGCCTCTCAAACCCTCCTTTCCCGCTTCGCCTTCCCAGCTCCCCCTTGCCACCCCACCCT T G KIF18B Ensembl:ENSG00000186185 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:44932213..44932396;chr17:44932226..44932336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_49576,Human_RBP_ID_17080287,Human_RBP_ID_17893694,Human_RBP_ID_18941774,Human_RBP_ID_22499610,Human_RBP_ID_22804918,Human_RBP_ID_22952141,Human_RBP_ID_25289279 RMVar_hsa_circ_6898,RMVar_hsa_circ_31547,RMVar_hsa_circ_371371,RMVar_hsa_circ_75893,RMVar_hsa_circ_184772,RMVar_hsa_circ_11210,RMVar_hsa_circ_184774 112335 RMVar_ID_112335 Human_SNP_ID_828062294 m1A Human chr17 + 7572883 7572883 7572883 AGCCAGGATTCCCGGTAAGAAAGGCATTTGCAAGAGATTGTGGCTGCTTATTTTGCCGCCCCCTT AGCCAGGATTCCCGGTAAGAAAGGCATTTGCATGAGATTGTGGCTGCTTATTTTGCCGCCCCCTT A T SENP3-EIF4A1,EIF4A1,AC016876.3 Ensembl:ENSG00000277957,Ensembl:ENSG00000161960,Ensembl:ENSG00000264772 Protein coding,Protein coding,lincRNA intron,intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7572876..7573249 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_13175602,Human_RBP_ID_18419529,Human_RBP_ID_19078291 RMVar_hsa_circ_82974,RMVar_hsa_circ_83453,RMVar_hsa_circ_125763,RMVar_hsa_circ_181881,RMVar_hsa_circ_102796,RMVar_hsa_circ_181883,RMVar_hsa_circ_181884,RMVar_hsa_circ_181885 112336 RMVar_ID_112336 Human_SNP_ID_828063978 m1A Human chr17 - 29589578 29589578 29589578 GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGAGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC GCCGCGAGCGGCGGCGGGGCGGCGCGGGGCGGGGGGCGCCCGAGGGCGAGCGGGCAGGCGGGCAC T C GIT1 Ensembl:ENSG00000108262 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:29589248..29589634;chr17:29589236..29589650;chr17:29589490..29589631 26863196 MeRIP-seq:(Medium) rs998008746 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_262597,Human_RBP_ID_768158,Human_RBP_ID_4464451,Human_RBP_ID_5185108,Human_RBP_ID_18419926,Human_RBP_ID_26782162 112337 RMVar_ID_112337 Human_SNP_ID_828066412 m1A Human chr17 - 81860484 81860484 81860484 TCCCGGCGGCGCCAACCGAAGCGCCCCGCCTGATCCGTGTCCGACATGCTGCGCCGCGCTCTGCT TCCCGGCGGCGCCAACCGAAGCGCCCCGCCTGCTCCGTGTCCGACATGCTGCGCCGCGCTCTGCT T G P4HB Ensembl:ENSG00000185624 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81860370..81860550 26863196 MeRIP-seq:(Medium) rs1130664 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_132144,Human_RBP_ID_820473,Human_RBP_ID_902057,Human_RBP_ID_1545041,Human_RBP_ID_4459677,Human_RBP_ID_9326975,Human_RBP_ID_18711884,Human_RBP_ID_22444047,Human_RBP_ID_22532922,Human_RBP_ID_26456503,Human_RBP_ID_26974945,Human_RBP_ID_27458981 Human_miRNA_ID_1938345,Human_miRNA_ID_1949445 RMVar_hsa_circ_118621,RMVar_hsa_circ_100494,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_94283,RMVar_hsa_circ_187773 112338 RMVar_ID_112338 Human_SNP_ID_828067101 m1A Human chr17 + 35135325 35135325 35135325 GGCACTAGCCACGATGCGGGAGTCAGGAGAGAAGAGCACCTGGTTGATGAGAGCTTGGTGTCCTG GGCACTAGCCACGATGCGGGAGTCAGGAGAGATGAGCACCTGGTTGATGAGAGCTTGGTGTCCTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:35135275..35136191 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 3 skin,head and neck 112339 RMVar_ID_112339 Human_SNP_ID_828084398 m1A Human chr17 - 19977746 19977746 19977746 CATCCCGAGGAGGCGGTGGGGCCCACTCCCGGAAGAAGGGTCCCTTTTCGCGCTAGTGCAGCGGC CATCCCGAGGAGGCGGTGGGGCCCACTCCCGGCAGAAGGGTCCCTTTTCGCGCTAGTGCAGCGGC T G AKAP10 Ensembl:ENSG00000108599 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19977700..19977790 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_237656,Human_RBP_ID_484877,Human_RBP_ID_4410876,Human_RBP_ID_17886884,Human_RBP_ID_18990712,Human_RBP_ID_26331381 112340 RMVar_ID_112340 Human_SNP_ID_828091132 m1A Human chr17 - 81665149 81665149 81665149 CTACCGCAGGACGGAGTCCAGGACGCAGCCGCAGCCTCCTTCCTTCACACCCCCTCACAGACTCC CTACCGCAGGACGGAGTCCAGGACGCAGCCGCGGCCTCCTTCCTTCACACCCCCTCACAGACTCC T C OXLD1 Ensembl:ENSG00000204237 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:81665101..81665325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_238325,Human_RBP_ID_502617 112341 RMVar_ID_112341 Human_SNP_ID_828101153 m1A Human chr17 + 1684425 1684425 1684425 GGGAGGGTCCCCACCCGCCTGCGCGCGCGCACACCCGCCCCGCCTCCGGCCCGCGCGCCGCTCCA GGGAGGGTCCCCACCCGCCTGCGCGCGCGCACCCCCGCCCCGCCTCCGGCCCGCGCGCCGCTCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:1684424..1684575;chr17:1684424..1684600 26863196 MeRIP-seq:(Medium) rs751976476 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112342 RMVar_ID_112342 Human_SNP_ID_828102499 m1A Human chr17 + 58631745 58631745 58631745 AACACTGCTATCCCACTCGTGAGAGAACACAAATATCTCCCTCTCGCGGTTTCCAGCGTTCTACA AACACTGCTATCCCACTCGTGAGAGAACACAAGTATCTCCCTCTCGCGGTTTCCAGCGTTCTACA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58631695..58631760 26863196 MeRIP-seq:(Medium) rs767252500 Functional Loss SNV ICGC 33..33 33 MELA 1 - 112343 RMVar_ID_112343 Human_SNP_ID_828103305 m1A Human chr17 + 82058944 82058944 82058944 CGTCCATGCCAGCTGTGGCCAGCCAGGCCAGGAGGCTCAGGGAGGGCAGAGGATGCAGGCTGGCC CGTCCATGCCAGCTGTGGCCAGCCAGGCCAGGTGGCTCAGGGAGGGCAGAGGATGCAGGCTGGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82058941..82059091 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112344 RMVar_ID_112344 Human_SNP_ID_828105683 m1A Human chr17 - 51260852 51260852 51260852 CTCGACGTCGCCGAAGACCAGCTCCTCCAAGCACCGCTCCACGGCCGGTTTGTCCTCCTCCAGCC CTCGACGTCGCCGAAGACCAGCTCCTCCAAGCGCCGCTCCACGGCCGGTTTGTCCTCCTCCAGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:51260801..51260875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 112345 RMVar_ID_112345 Human_SNP_ID_828106936 m1A Human chr17 + 1880596 1880596 1880596 AGACAGCCCGTGTTGGCTATCAAAGGAGCCCGAGTCTCTGATTTCGGTGGACGGAGCCTCTCCGT AGACAGCCCGTGTTGGCTATCAAAGGAGCCCGTGTCTCTGATTTCGGTGGACGGAGCCTCTCCGT A T - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cells, overexperss TRMT6;HTR8/Svneo,Normoxia chr17:1880546..1880647 29072297,32194978 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112346 RMVar_ID_112346 Human_SNP_ID_828110720 m1A Human chr17 - 18383365 18383365 18383365 CGCCCTGCCCCCAGCGCACCTGGATGGGCCCCACCGCGGGGTGCCGCAGCTCCACCATGCGCTTG CGCCCTGCCCCCAGCGCACCTGGATGGGCCCCCCCGCGGGGTGCCGCAGCTCCACCATGCGCTTG T G AL353997.2 Ensembl:ENSG00000264177 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:18383317..18383578 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 112347 RMVar_ID_112347 Human_SNP_ID_828115173 m1A Human chr17 + 28661840 28661840 28661840 GACACCCAGGCTGGACGCTCCCACAGCGCTCCACAAACCCCCCAACAACAGCAGAGGTACTACAG GACACCCAGGCTGGACGCTCCCACAGCGCTCCGCAAACCCCCCAACAACAGCAGAGGTACTACAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28661790..28661940 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 112348 RMVar_ID_112348 Human_SNP_ID_828115274 m1A Human chr17 - 35151325 35151325 35151325 TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGAAATGTGGCGTACGGAAGACCCACTCCCCGGCGC TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGACATGTGGCGTACGGAAGACCCACTCCCCGGCGC T G - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs62062411 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III,lung small_cell_carcinoma 9 lung,brain Human_RBP_ID_269922,Human_RBP_ID_1091851,Human_RBP_ID_4471122,Human_RBP_ID_5189099,Human_RBP_ID_5274904,Human_RBP_ID_5577105,Human_RBP_ID_6662142,Human_RBP_ID_8093684,Human_RBP_ID_8816448,Human_RBP_ID_9078515,Human_RBP_ID_9856148,Human_RBP_ID_10483404,Human_RBP_ID_12970340,Human_RBP_ID_17063131,Human_RBP_ID_17190239,Human_RBP_ID_17259158,Human_RBP_ID_17691787,Human_RBP_ID_17889976,Human_RBP_ID_18179330,Human_RBP_ID_18200138,Human_RBP_ID_18207789,Human_RBP_ID_22212303,Human_RBP_ID_22390159,Human_RBP_ID_22960547,Human_RBP_ID_23275477,Human_RBP_ID_23308819,Human_RBP_ID_23721728,Human_RBP_ID_24415132,Human_RBP_ID_24478587,Human_RBP_ID_25272833,Human_RBP_ID_26449279,Human_RBP_ID_27156502,Human_RBP_ID_27451062 112349 RMVar_ID_112349 Human_SNP_ID_828118367 m1A Human chr17 - 5408766 5408766 5408766 ATACCCACTGTACATCTTATATGAAAATGGAGAGACTTTCCTGACATACATCAGTCTGTTACACA ATACCCACTGTACATCTTATATGAAAATGGAGGGACTTTCCTGACATACATCAGTCTGTTACACA T C NUP88 Ensembl:ENSG00000108559 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5405226..5408816 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_300765,Human_RBP_ID_1537549,Human_RBP_ID_1863292,Human_RBP_ID_13079768,Human_RBP_ID_23735735 Human_Splice_Rec_1766737,Human_Splice_Rec_1766769,Human_Splice_Rec_1766825 Human_miRNA_ID_2048251 RMVar_hsa_circ_573,RMVar_hsa_circ_81020,RMVar_hsa_circ_181644,RMVar_hsa_circ_311252,RMVar_hsa_circ_181656,RMVar_hsa_circ_70125,RMVar_hsa_circ_181652,RMVar_hsa_circ_282733,RMVar_hsa_circ_343937,RMVar_hsa_circ_282297,RMVar_hsa_circ_181657,RMVar_hsa_circ_57360,RMVar_hsa_circ_181658,RMVar_hsa_circ_316116,RMVar_hsa_circ_181655,RMVar_hsa_circ_342748,RMVar_hsa_circ_293496,RMVar_hsa_circ_123232,RMVar_hsa_circ_290398,RMVar_hsa_circ_341617,RMVar_hsa_circ_181659,RMVar_hsa_circ_181660,RMVar_hsa_circ_102176,RMVar_hsa_circ_375246,RMVar_hsa_circ_181661,RMVar_hsa_circ_181662 112350 RMVar_ID_112350 Human_SNP_ID_828125643 m1A Human chr17 - 81717472 81717472 81717472 GCCGGCCACTTACTGCAATAAAGCTGGCGACAAAGTGAGTGAAGATGTTGTCAGAGAGGTACCCG GCCGGCCACTTACTGCAATAAAGCTGGCGACACAGTGAGTGAAGATGTTGTCAGAGAGGTACCCG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:81716850..81717472 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112351 RMVar_ID_112351 Human_SNP_ID_828127672 m1A Human chr17 - 43493543 43493543 43493543 TGGTCTTGGTCCCAGTGAAGGACAGCACTTTGACTTTGACCCTCTGGCCTTTGCTCACGACATCA TGGTCTTGGTCCCAGTGAAGGACAGCACTTTGGCTTTGACCCTCTGGCCTTTGCTCACGACATCA T C lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43493494..43493582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112352 RMVar_ID_112352 Human_SNP_ID_828130437 m1A Human chr17 - 413438 413438 413438 GGGGTCGGGGTGGAAGCCCTTGAGGGCCAAGCACCGGTACCGTTTTCTCCGATTCAGTTTATAGA GGGGTCGGGGTGGAAGCCCTTGAGGGCCAAGCGCCGGTACCGTTTTCTCCGATTCAGTTTATAGA T C AC141424.1 Ensembl:ENSG00000241525 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:413418..413616 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 3 oesophagus 112353 RMVar_ID_112353 Human_SNP_ID_828142501 m1A Human chr17 + 81200444 81200444 81200444 TGGTGACAGTGGCCTGGTTCACCTGGTGGATAAACCTGCCCGGAGAGCAGGACTCAGGGCCAAGA TGGTGACAGTGGCCTGGTTCACCTGGTGGATACACCTGCCCGGAGAGCAGGACTCAGGGCCAAGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81200300..81200457 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112354 RMVar_ID_112354 Human_SNP_ID_828142678 m1A Human chr17 - 42536301 42536301 42536301 CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCACCGCCGCGGCCACCGCCACCGCCTCCATGGTC CGCCCCCGGCCCCGGCCAGGAGAAGGACCCCCCCCGCCGCGGCCACCGCCACCGCCTCCATGGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:42536251..42538341;chr17:42536251..42536946 26863196 MeRIP-seq:(Medium) rs794726879 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112355 RMVar_ID_112355 Human_SNP_ID_828142837 m1A Human chr17 + 40177469 40177469 40177469 ACTGGAGGAGGGGGCGCGGTCTCGGTTCTGCCACCTTCCCCCTCTTCACGGCCAGGAGCGCAGCC ACTGGAGGAGGGGGCGCGGTCTCGGTTCTGCCCCCTTCCCCCTCTTCACGGCCAGGAGCGCAGCC A C RAPGEFL1 Ensembl:ENSG00000108352 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40177421..40177575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8727432,Human_RBP_ID_22716537 112356 RMVar_ID_112356 Human_SNP_ID_828149026 m1A Human chr17 - 7674892 7674892 7674892 GTGGAGTATTTGGATGACAGAAACACTTTTCGACATAGTGTGGTGGTGCCCTATGAGCCGCCTGA GTGGAGTATTTGGATGACAGAAACACTTTTCGGCATAGTGTGGTGGTGCCCTATGAGCCGCCTGA T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs1800372 Functional Loss SNV COSMIC 33..33 33 meninges atypical,breast ER-positive_carcinoma,colon adenocarcinoma,brain oligodendroglioma_Grade_II,central_nervous_system oligodendroglioma_Grade_II,haematopoietic_and_lymphoid_tissue myelodysplastic_syndrome,large_intestine adenocarcinoma 171 large intestine,haematopoietic and lymphoid tissue,brain,breast Human_RBP_ID_501217,Human_RBP_ID_1543366,Human_RBP_ID_1869944,Human_RBP_ID_18296710,Human_RBP_ID_23751550,Human_RBP_ID_27457648 Human_Splice_Rec_1773746,Human_Splice_Rec_1773747,Human_Splice_Rec_1773760,Human_Splice_Rec_1773761,Human_Splice_Rec_1773780,Human_Splice_Rec_1773781,Human_Splice_Rec_1773790,Human_Splice_Rec_1773791,Human_Splice_Rec_1773804,Human_Splice_Rec_1773805,Human_Splice_Rec_1773818,Human_Splice_Rec_1773819,Human_Splice_Rec_1773830,Human_Splice_Rec_1773831,Human_Splice_Rec_1773842,Human_Splice_Rec_1773843,Human_Splice_Rec_1773856,Human_Splice_Rec_1773857,Human_Splice_Rec_1773876,Human_Splice_Rec_1773877,Human_Splice_Rec_1773896,Human_Splice_Rec_1773897,Human_Splice_Rec_1773916,Human_Splice_Rec_1773917,Human_Splice_Rec_1773936,Human_Splice_Rec_1773937,Human_Splice_Rec_1773958,Human_Splice_Rec_1773959,Human_Splice_Rec_1773980,Human_Splice_Rec_1773981,Human_Splice_Rec_1774002,Human_Splice_Rec_1774003,Human_Splice_Rec_1774024,Human_Splice_Rec_1774025,Human_Splice_Rec_1774046,Human_Splice_Rec_1774047,Human_Splice_Rec_1774066,Human_Splice_Rec_1774067,Human_Splice_Rec_1774084,Human_Splice_Rec_1774085,Human_Splice_Rec_1774098,Human_Splice_Rec_1774099,Human_Splice_Rec_1774112,Human_Splice_Rec_1774113,Human_Splice_Rec_1774124 Clinvar_Rec_655 GWAS_ID_13658,GWAS_ID_13659,GWAS_ID_13660,GWAS_ID_13661,GWAS_ID_13662,GWAS_ID_13663,GWAS_ID_13664,GWAS_ID_13665,GWAS_ID_13666,GWAS_ID_13667,GWAS_ID_13668,GWAS_ID_13669,GWAS_ID_13670,GWAS_ID_13671,GWAS_ID_13672 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112357 RMVar_ID_112357 Human_SNP_ID_828156665 m1A Human chr17 - 50199302 50199302 50199302 CCTGCAGGGACCCGCAGGCCCCCCTGGCCGAGATGGCATCCCTGGACAGCCTGGACTTCCCGGAC CCTGCAGGGACCCGCAGGCCCCCCTGGCCGAGTTGGCATCCCTGGACAGCCTGGACTTCCCGGAC T A COL1A1 Ensembl:ENSG00000108821 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:50199251..50199350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_Splice_Rec_1837460,Human_Splice_Rec_1837461,Human_Splice_Rec_1837618,Human_Splice_Rec_1837624 RMVar_hsa_circ_86750,RMVar_hsa_circ_101128,RMVar_hsa_circ_121288,RMVar_hsa_circ_185269,RMVar_hsa_circ_185270,RMVar_hsa_circ_102180,RMVar_hsa_circ_185276,RMVar_hsa_circ_112302,RMVar_hsa_circ_185278,RMVar_hsa_circ_185290,RMVar_hsa_circ_76467,RMVar_hsa_circ_185296,RMVar_hsa_circ_103651,RMVar_hsa_circ_105520,RMVar_hsa_circ_185298,RMVar_hsa_circ_185299,RMVar_hsa_circ_185300,RMVar_hsa_circ_109292,RMVar_hsa_circ_116255,RMVar_hsa_circ_185307,RMVar_hsa_circ_77548,RMVar_hsa_circ_185306,RMVar_hsa_circ_84453,RMVar_hsa_circ_185310,RMVar_hsa_circ_97631,RMVar_hsa_circ_185315 112358 RMVar_ID_112358 Human_SNP_ID_828156693 m1A Human chr17 - 7675149 7675143 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGC______GTCCGCGCCATGGCCATCTACAAGCAG CGCGGGT C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) rs1555526166 Functional Loss DEL TCGA,ICGC 33..38 33 PBCA,OV 3 - Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 Clinvar_Rec_656 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112359 RMVar_ID_112359 Human_SNP_ID_828157372 m1A Human chr17 + 77498513 77498513 77498513 CTGCGCCCACCTCACTGACCCGCCCGCCCCCCACCCCCACAGGACGCACATGCAGAACATCAAGG CTGCGCCCACCTCACTGACCCGCCCGCCCCCCCCCCCCACAGGACGCACATGCAGAACATCAAGG A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:77498501..77498747 32194978 MeRIP-seq:(Medium) rs773443029 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 15 liver 112360 RMVar_ID_112360 Human_SNP_ID_828159514 m1A Human chr17 - 40818884 40818867 40818885 GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC GCGGCTACGGGGGCGGCAGCTCCGGCGGCGG__________________ATACGGCGGCGGCAGC TCCGCCGCCGGAGCTGCTG T KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40818776..40818999 26863410 MeRIP-seq:(Medium) rs766129021 Functional Loss DEL ICGC 32..49 33 COCA 1 - Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4425768,Human_RBP_ID_5496986,Human_RBP_ID_8941820,Human_RBP_ID_18419596 Human_Splice_Rec_1815551 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 112361 RMVar_ID_112361 Human_SNP_ID_828162325 m1A Human chr17 - 47189217 47189217 47189217 TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACAGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC TGAGCAGGGGCTGGCCGGGCCGGAGCCGCTACGGGGGGGGCCTGAGGCACTGCAGAAAGTGGGCC T C CDC27 Ensembl:ENSG00000004897 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:47189143..47189275;chr17:47189125..47189237 26863196 MeRIP-seq:(Medium) rs79580708 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 4 brain Human_RBP_ID_235478,Human_RBP_ID_491808,Human_RBP_ID_764181,Human_RBP_ID_819124,Human_RBP_ID_4433611,Human_RBP_ID_18420593,Human_RBP_ID_26333484 Human_Splice_Rec_1831501,Human_Splice_Rec_1831537,Human_Splice_Rec_1831577,Human_Splice_Rec_1831621,Human_Splice_Rec_1831657,Human_Splice_Rec_1831687,Human_Splice_Rec_1831747,Human_Splice_Rec_1831759,Human_Splice_Rec_1831789 RMVar_hsa_circ_121510,RMVar_hsa_circ_184903 112362 RMVar_ID_112362 Human_SNP_ID_828163233 m1A Human chr17 + 48056488 48056485 48056488 ATAGTCACCGCCAGAAGGAGCAGGATGTGGAGAAGGAGCTGCGAGATGGAGGCGAGCAGGACACC ATAGTCACCGCCAGAAGGAGCAGGATGTGG___AGGAGCTGCGAGATGGAGGCGAGCAGGACACC GAGA G NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48056438..48056600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 LICA 1 - Human_RBP_ID_3526718,Human_RBP_ID_4434624,Human_RBP_ID_6606501,Human_RBP_ID_8819095,Human_RBP_ID_17905792,Human_RBP_ID_18191293,Human_RBP_ID_22444725,Human_RBP_ID_26331990 Human_Splice_Rec_1834036,Human_Splice_Rec_1834088,Human_Splice_Rec_1834100 Human_miRNA_ID_1540846,Human_miRNA_ID_1594444 RMVar_hsa_circ_10429,RMVar_hsa_circ_350476 112363 RMVar_ID_112363 Human_SNP_ID_828163884 m1A Human chr17 + 62424048 62424048 62424048 ATCACTCTGCCCCTTCGCCCGGCCTGTCGCTGACCCTCTGTCCCGCCGCCTCGGAGCACTCCGAA ATCACTCTGCCCCTTCGCCCGGCCTGTCGCTGGCCCTCTGTCCCGCCGCCTCGGAGCACTCCGAA A G METTL2A Ensembl:ENSG00000087995 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11543000 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_19083460 GWAS_ID_13073,GWAS_ID_13074 112364 RMVar_ID_112364 Human_SNP_ID_828173001 m1A Human chr17 + 76021513 76021513 76021513 TCCACGTGCTGCAGCTGGGTCTCCTGGCAGATACACAGGTTCAGGAAGTTCTGCCACTCCATCTT TCCACGTGCTGCAGCTGGGTCTCCTGGCAGATGCACAGGTTCAGGAAGTTCTGCCACTCCATCTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76021482..76021566 26863196 MeRIP-seq:(Medium) rs193119748 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,mouth squamous_cell_carcinoma,liver neoplasm,large_intestine adenocarcinoma,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 20 liver,bladder,urinary tract,head and neck,large intestine 112365 RMVar_ID_112365 Human_SNP_ID_828173211 m1A Human chr17 - 44967970 44967970 44967970 GCGGCCCGGAAGGCCACTATGAGATGCTGGGCACCTGCCGCATGGTGTGCGACCCCTACCCCGCG GCGGCCCGGAAGGCCACTATGAGATGCTGGGCCCCTGCCGCATGGTGTGCGACCCCTACCCCGCG T G C1QL1 Ensembl:ENSG00000131094 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44967922..44968298 26863196 MeRIP-seq:(Medium) rs770780187 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate Human_RBP_ID_491253 112366 RMVar_ID_112366 Human_SNP_ID_828173438 m1A Human chr17 + 82738567 82738567 82738567 GGAGCACGGGCCTGGTGCGGGTGCCGAGGCCCATGAAGGTCATCGACCTGCCGGGAGGTGGGGCC GGAGCACGGGCCTGGTGCGGGTGCCGAGGCCCCTGAAGGTCATCGACCTGCCGGGAGGTGGGGCC A C FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82738516..82738679 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_3542200,Human_RBP_ID_4467430,Human_RBP_ID_5318743,Human_RBP_ID_9379426,Human_RBP_ID_18989787,Human_RBP_ID_20292177 Human_Splice_Rec_1886476,Human_Splice_Rec_1886477,Human_Splice_Rec_1886486,Human_Splice_Rec_1886487,Human_Splice_Rec_1886490,Human_Splice_Rec_1886491,Human_Splice_Rec_1886497 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 112367 RMVar_ID_112367 Human_SNP_ID_828175935 m1A Human chr17 + 43002800 43002800 43002800 TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTAGTGAATGGTGGAGTATGGTTTCACTATTTCCA TCAAGTTTGAAGAGAGGTAAGTAGGCTTTGGTCGTGAATGGTGGAGTATGGTTTCACTATTTCCA A C RPL27 Ensembl:ENSG00000131469 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11871636 Functional Loss SNV ICGC 33..33 33 COCA 5 - GWAS_ID_15226,GWAS_ID_15227,GWAS_ID_15228,GWAS_ID_15229 RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_184521,RMVar_hsa_circ_184524,RMVar_hsa_circ_107591,RMVar_hsa_circ_184525 112368 RMVar_ID_112368 Human_SNP_ID_828176987 m1A Human chr17 - 79834870 79834864 79834870 GGGGCAAGATGAAGATAGTCAAGAACAAGAACAAGAACGGACGCATCGTGATCGTGATGAGCAAA GGGGCAAGATGAAGATAGTCAAGAACAAGAAC______GGACGCATCGTGATCGTGATGAGCAAA CGTTCTT C CBX4 Ensembl:ENSG00000141582 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:79833720..79835392 26863196 MeRIP-seq:(Medium) rs1388431022 Functional Loss DEL ICGC 33..38 33 CHOL 1 - Human_RBP_ID_1543865,Human_RBP_ID_1870281,Human_RBP_ID_3538746,Human_RBP_ID_8253780,Human_RBP_ID_13185882,Human_RBP_ID_18530961 RMVar_hsa_circ_78987,RMVar_hsa_circ_187441 112369 RMVar_ID_112369 Human_SNP_ID_828182549 m1A Human chr17 - 40417822 40417822 40417822 TCTCGTGGGGTCCTGCCTGTTTAGTCGCTTTCAGGGTTCTTGAGCCCCTTCACGACCGTCACCAT TCTCGTGGGGTCCTGCCTGTTTAGTCGCTTTCGGGGTTCTTGAGCCCCTTCACGACCGTCACCAT T C TOP2A Ensembl:ENSG00000131747 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:40417751..40417900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_50592,Human_RBP_ID_133380,Human_RBP_ID_1857766,Human_RBP_ID_2505805,Human_RBP_ID_3522835,Human_RBP_ID_4465361,Human_RBP_ID_8817679,Human_RBP_ID_9071856,Human_RBP_ID_9257855,Human_RBP_ID_9289057,Human_RBP_ID_9326613,Human_RBP_ID_18697316,Human_RBP_ID_23118888,Human_RBP_ID_26960541,Human_RBP_ID_27665028 Human_Splice_Rec_1814523 112370 RMVar_ID_112370 Human_SNP_ID_828185813 m1A Human chr17 - 75809812 75809812 75809812 GTGGAAGCAGGTGTAGGGCCGATGCTGCGTGCATTTGTGTTGCACAAAGAGTGGGCACTGCTCTG GTGGAAGCAGGTGTAGGGCCGATGCTGCGTGCGTTTGTGTTGCACAAAGAGTGGGCACTGCTCTG T C lnc-SRP68-1 RNACentral:URS00008BF89B lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75809727..75809830 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 112371 RMVar_ID_112371 Human_SNP_ID_828186652 m1A Human chr17 - 40818899 40818899 40818899 CCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGA CCGGCGGCGGCGGCGGCGGCTACGGGGGCGGCGGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGA T C KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:40818776..40819037 26863196 MeRIP-seq:(Medium) rs1217847176 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,oesophagus squamous_cell_carcinoma,ESCA 3 oesophagus,head and neck Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4464537,Human_RBP_ID_8941820,Human_RBP_ID_18419596 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 112372 RMVar_ID_112372 Human_SNP_ID_828188755 m1A Human chr17 + 62606142 62606142 62606142 ATATTTCTTTTTTGTCCCAGGTATTTACCACCAGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA ATATTTCTTTTTTGTCCCAGGTATTTACCACCGGAGTGTTTTGTGGTTGGGAAAGAACCACCAAA A G TLK2 Ensembl:ENSG00000146872 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8078132 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_9346369,Human_RBP_ID_22586633,Human_RBP_ID_22656637 Human_Splice_Rec_1850550,Human_Splice_Rec_1850551,Human_Splice_Rec_1850642,Human_Splice_Rec_1850643,Human_Splice_Rec_1850686,Human_Splice_Rec_1850687,Human_Splice_Rec_1850726,Human_Splice_Rec_1850727,Human_Splice_Rec_1850774,Human_Splice_Rec_1850796,Human_Splice_Rec_1850797 GWAS_ID_13075,GWAS_ID_13076,GWAS_ID_13077 RMVar_hsa_circ_1739,RMVar_hsa_circ_105826,RMVar_hsa_circ_186202,RMVar_hsa_circ_23423,RMVar_hsa_circ_108797,RMVar_hsa_circ_186219,RMVar_hsa_circ_186227,RMVar_hsa_circ_108597,RMVar_hsa_circ_186224,RMVar_hsa_circ_316047,RMVar_hsa_circ_325245,RMVar_hsa_circ_186228,RMVar_hsa_circ_342126 112373 RMVar_ID_112373 Human_SNP_ID_828192819 m1A Human chr17 + 43769149 43769149 43769149 GTGGAAGGCTGTGGGGACAGTGCAGGGCACAGACGTGGTGGGGAGAGTGGCCTGCATTTGCATAG GTGGAAGGCTGTGGGGACAGTGCAGGGCACAGCCGTGGTGGGGAGAGTGGCCTGCATTTGCATAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:43769126..43769150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112374 RMVar_ID_112374 Human_SNP_ID_828198383 m1A Human chr17 + 59946914 59946914 59946914 CAGAGAGTCAATGTCATTACATAGAACACTTCAGACACAGGAAAAATAAACGTGGATTTTAAAAA CAGAGAGTCAATGTCATTACATAGAACACTTCGGACACAGGAAAAATAAACGTGGATTTTAAAAA A G AC005702.1,RPS6KB1 Ensembl:ENSG00000267318,Ensembl:ENSG00000108443 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs180515 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1538977,Human_RBP_ID_1865019,Human_RBP_ID_13107741,Human_RBP_ID_23740152,Human_RBP_ID_26460826,Human_RBP_ID_26967866,Human_RBP_ID_27257758 GWAS_ID_12940,GWAS_ID_12941,GWAS_ID_12942,GWAS_ID_12943,GWAS_ID_12944,GWAS_ID_12945,GWAS_ID_12946,GWAS_ID_12947,GWAS_ID_12948,GWAS_ID_12949,GWAS_ID_12950,GWAS_ID_12951 RMVar_hsa_circ_126034,RMVar_hsa_circ_185887 112375 RMVar_ID_112375 Human_SNP_ID_828201826 m1A Human chr17 - 82805977 82805977 82805977 ATCACACGCTCCACCCCCTCTGGGACGTCGTCATCTTCGTCGTCATCTTCGGTCAGGATGAGTGG ATCACACGCTCCACCCCCTCTGGGACGTCGTCTTCTTCGTCGTCATCTTCGGTCAGGATGAGTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82805927..82806058 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast 112376 RMVar_ID_112376 Human_SNP_ID_828202495 m1A Human chr17 + 30185554 30185554 30185554 AAGGGTAAAGAACAAGAGAGACCACCTGAGGCAGTGAGCAAGTTTGCAAAGCGGAACAATGAAGA AAGGGTAAAGAACAAGAGAGACCACCTGAGGCTGTGAGCAAGTTTGCAAAGCGGAACAATGAAGA A T NSRP1 Ensembl:ENSG00000126653 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:30185504..30185624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary Human_RBP_ID_23719299 Human_miRNA_ID_1310198 112377 RMVar_ID_112377 Human_SNP_ID_828203260 m1A Human chr17 - 59081144 59081144 59081144 AACACGTCACTAAAGTGAATGAAGAGGTAGCCAAACTTCGTCGGCGTCTCATGGAACTGATCAGC AACACGTCACTAAAGTGAATGAAGAGGTAGCCCAACTTCGTCGGCGTCTCATGGAACTGATCAGC T G TRIM37 Ensembl:ENSG00000108395 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:59081054..59081200;chr17:59081058..59081160 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary Human_RBP_ID_13099939 Human_Splice_Rec_1846706,Human_Splice_Rec_1846707,Human_Splice_Rec_1846756,Human_Splice_Rec_1846757,Human_Splice_Rec_1846800,Human_Splice_Rec_1846801,Human_Splice_Rec_1846844,Human_Splice_Rec_1846845,Human_Splice_Rec_1846881,Human_Splice_Rec_1846916,Human_Splice_Rec_1846917 RMVar_hsa_circ_313386,RMVar_hsa_circ_2033,RMVar_hsa_circ_185682,RMVar_hsa_circ_33718,RMVar_hsa_circ_284542,RMVar_hsa_circ_375375,RMVar_hsa_circ_185696,RMVar_hsa_circ_185698,RMVar_hsa_circ_185697,RMVar_hsa_circ_106105,RMVar_hsa_circ_185709,RMVar_hsa_circ_185703,RMVar_hsa_circ_371211,RMVar_hsa_circ_335074,RMVar_hsa_circ_350749,RMVar_hsa_circ_185708,RMVar_hsa_circ_278743,RMVar_hsa_circ_185710,RMVar_hsa_circ_331248,RMVar_hsa_circ_185719,RMVar_hsa_circ_376690,RMVar_hsa_circ_52843,RMVar_hsa_circ_185725,RMVar_hsa_circ_185726,RMVar_hsa_circ_349656,RMVar_hsa_circ_376507,RMVar_hsa_circ_303374,RMVar_hsa_circ_284967,RMVar_hsa_circ_25861,RMVar_hsa_circ_103840,RMVar_hsa_circ_185727,RMVar_hsa_circ_185728,RMVar_hsa_circ_315596,RMVar_hsa_circ_288790,RMVar_hsa_circ_185734,RMVar_hsa_circ_291329,RMVar_hsa_circ_313544,RMVar_hsa_circ_185735,RMVar_hsa_circ_41403,RMVar_hsa_circ_41589,RMVar_hsa_circ_185739,RMVar_hsa_circ_185740,RMVar_hsa_circ_185738,RMVar_hsa_circ_301787,RMVar_hsa_circ_323884,RMVar_hsa_circ_314935,RMVar_hsa_circ_288278,RMVar_hsa_circ_17756,RMVar_hsa_circ_185741,RMVar_hsa_circ_185743,RMVar_hsa_circ_185744,RMVar_hsa_circ_185742,RMVar_hsa_circ_289353,RMVar_hsa_circ_22630,RMVar_hsa_circ_349303,RMVar_hsa_circ_73368,RMVar_hsa_circ_314749,RMVar_hsa_circ_325782,RMVar_hsa_circ_341307,RMVar_hsa_circ_316664,RMVar_hsa_circ_185747,RMVar_hsa_circ_185748,RMVar_hsa_circ_276846,RMVar_hsa_circ_337675,RMVar_hsa_circ_265955,RMVar_hsa_circ_185751,RMVar_hsa_circ_185749,RMVar_hsa_circ_185750,RMVar_hsa_circ_343951,RMVar_hsa_circ_369804 112378 RMVar_ID_112378 Human_SNP_ID_828205314 m1A Human chr17 - 41803379 41803379 41803379 ACCGCCCCTGGAGCCTGAGGATGCCCTATCTGACGCCGAGTTTGAGGGGGAGGGTGACTACGAGG ACCGCCCCTGGAGCCTGAGGATGCCCTATCTGGCGCCGAGTTTGAGGGGGAGGGTGACTACGAGG T C P3H4 Ensembl:ENSG00000141696 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:41803240..41803469 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_22761470 Human_Splice_Rec_1816634,Human_Splice_Rec_1816635,Human_Splice_Rec_1816648,Human_Splice_Rec_1816649,Human_Splice_Rec_1816652,Human_Splice_Rec_1816653,Human_Splice_Rec_1816656,Human_Splice_Rec_1816657 Human_miRNA_ID_2017991,Human_miRNA_ID_2517544 RMVar_hsa_circ_77359,RMVar_hsa_circ_105661,RMVar_hsa_circ_90167,RMVar_hsa_circ_102394,RMVar_hsa_circ_82902,RMVar_hsa_circ_184204,RMVar_hsa_circ_184206,RMVar_hsa_circ_184207,RMVar_hsa_circ_184208,RMVar_hsa_circ_184205,RMVar_hsa_circ_184209,RMVar_hsa_circ_374419 112379 RMVar_ID_112379 Human_SNP_ID_828206882 m1A Human chr17 + 75763384 75763384 75763384 GCCACTTCCAAGGATGCTGAGCTGGACAGGCCACCCCCCAGGGGCACTGAGCTGACCACCACTGC GCCACTTCCAAGGATGCTGAGCTGGACAGGCCGCCCCCCAGGGGCACTGAGCTGACCACCACTGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:75763280..75763481 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112380 RMVar_ID_112380 Human_SNP_ID_828209255 m1A Human chr17 + 28570881 28570881 28570881 CACATTTCAGAGGAATCTCTCTTTCATGCACAACGGTGAAGGGCAGCTTCTCCTGGTCGTCCAGG CACATTTCAGAGGAATCTCTCTTTCATGCACAGCGGTGAAGGGCAGCTTCTCCTGGTCGTCCAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28456097..28583950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck 112381 RMVar_ID_112381 Human_SNP_ID_828210759 m1A Human chr17 - 75778835 75778835 75778835 CGCGCAGGATTTCAAAACCGACCTGAGGTTTCAGAGCGCAGCCATCGGTGCGCTGCAGGTAAGAC CGCGCAGGATTTCAAAACCGACCTGAGGTTTCGGAGCGCAGCCATCGGTGCGCTGCAGGTAAGAC T C H3-3B Ensembl:ENSG00000132475 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:75778643..75778880 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma 6 kidney Human_RBP_ID_500017,Human_RBP_ID_1542214,Human_RBP_ID_1869117,Human_RBP_ID_3537325,Human_RBP_ID_4464789,Human_RBP_ID_6644108,Human_RBP_ID_8463190,Human_RBP_ID_9076296,Human_RBP_ID_17900907,Human_RBP_ID_18708790,Human_RBP_ID_18992284,Human_RBP_ID_19079976,Human_RBP_ID_22443162,Human_RBP_ID_22807962,Human_RBP_ID_23749359,Human_RBP_ID_26971172,Human_RBP_ID_27259763 Human_Splice_Rec_1868881,Human_Splice_Rec_1868884,Human_Splice_Rec_1868885,Human_Splice_Rec_1868897,Human_Splice_Rec_1868903,Human_Splice_Rec_1868909,Human_Splice_Rec_1868915,Human_Splice_Rec_1868921,Human_Splice_Rec_1868929 RMVar_hsa_circ_32539 112382 RMVar_ID_112382 Human_SNP_ID_828213783 m1A Human chr17 + 81720077 81720077 81720077 CGCAAAAACTTTGGCATCAAAGTGCCATCCTGACCAGCCGTGGGAATGGCTGGGCTGCCAGGCCA CGCAAAAACTTTGGCATCAAAGTGCCATCCTGCCCAGCCGTGGGAATGGCTGGGCTGCCAGGCCA A C SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding CDS,stop codon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:81720026..81720967 32194978 MeRIP-seq:(Medium) rs763478303 Functional Loss SNV ICGC,COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,lung adenocarcinoma,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,brain astrocytoma_Grade_IV,right_lower_lobe adenocarcinoma,CLLE,kidney papillary_renal_cell_carcinoma 25 lung,kidney,haematopoietic and lymphoid tissue,brain Human_RBP_ID_502712,Human_RBP_ID_5115279,Human_RBP_ID_13199115,Human_RBP_ID_22445098,Human_RBP_ID_27262332 RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 112383 RMVar_ID_112383 Human_SNP_ID_828217975 m1A Human chr17 - 18247740 18247740 18247740 AGTCCCCGCGCCTGGTGCGCGCTGCCGCCCTCAAGCTGGGTCAGGAGCTGTGCGGGATGCTGCAC AGTCCCCGCGCCTGGTGCGCGCTGCCGCCCTCGAGCTGGGTCAGGAGCTGTGCGGGATGCTGCAC T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18247651..18247850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_236878,Human_RBP_ID_4409627,Human_RBP_ID_8824467,Human_RBP_ID_9288806,Human_RBP_ID_18190738,Human_RBP_ID_26331376 Human_Splice_Rec_1787595,Human_Splice_Rec_1787695,Human_Splice_Rec_1787753,Human_Splice_Rec_1787811,Human_Splice_Rec_1787893 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 112384 RMVar_ID_112384 Human_SNP_ID_828224746 m1A Human chr17 + 80964563 80964563 80964563 GGGCTCGGGTTGACGGTGGCTTCCCACTGAGCACCAGCATCCAGGTGCACCCCCGCGGCCACGGC GGGCTCGGGTTGACGGTGGCTTCCCACTGAGCGCCAGCATCCAGGTGCACCCCCGCGGCCACGGC A G RPTOR Ensembl:ENSG00000141564 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80964512..80964626 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_8465658,Human_RBP_ID_17654993 Human_miRNA_ID_272327,Human_miRNA_ID_2052583,Human_miRNA_ID_2751167 RMVar_hsa_circ_187548,RMVar_hsa_circ_83314,RMVar_hsa_circ_116660,RMVar_hsa_circ_187552 112385 RMVar_ID_112385 Human_SNP_ID_828228473 m1A Human chr17 - 36505093 36505093 36505093 TGGTTGTGTGGTCTGTGCATAGTAGCCTAGCCAGGGAGGCAAGTTCCAGTGCATCTTGTTTTTTT TGGTTGTGTGGTCTGTGCATAGTAGCCTAGCCTGGGAGGCAAGTTCCAGTGCATCTTGTTTTTTT T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:36505090..36505241 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_896417,Human_RBP_ID_1532297,Human_RBP_ID_1855747,Human_RBP_ID_2503090 Human_Splice_Rec_1806966 Human_miRNA_ID_335982 RMVar_hsa_circ_64427,RMVar_hsa_circ_324619 112386 RMVar_ID_112386 Human_SNP_ID_828238240 m1A Human chr17 + 40161904 40161904 40161904 AAGCACTGTGACTGGAGAGAGGCAAAGTGGGGACGGACAGGTTAGTACATTCCACAGTCCTCCAT AAGCACTGTGACTGGAGAGAGGCAAAGTGGGGGCGGACAGGTTAGTACATTCCACAGTCCTCCAT A G CASC3 Ensembl:ENSG00000108349 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:40141551..40162142 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,gastroesophageal_junction adenocarcinoma 1 stomach Human_RBP_ID_6807,Human_RBP_ID_200039,Human_RBP_ID_821992,Human_RBP_ID_899948,Human_RBP_ID_3952332,Human_RBP_ID_21975087,Human_RBP_ID_24372658,Human_RBP_ID_24544857,Human_RBP_ID_24552289,Human_RBP_ID_26331740,Human_RBP_ID_27812640 Human_Splice_Rec_1814027,Human_Splice_Rec_1814047,Human_Splice_Rec_1814073 RMVar_hsa_circ_83012,RMVar_hsa_circ_184020,RMVar_hsa_circ_115012,RMVar_hsa_circ_184018,RMVar_hsa_circ_269704,RMVar_hsa_circ_98384,RMVar_hsa_circ_184022,RMVar_hsa_circ_289239,RMVar_hsa_circ_337960,RMVar_hsa_circ_377536,RMVar_hsa_circ_184019,RMVar_hsa_circ_340698,RMVar_hsa_circ_305293,RMVar_hsa_circ_184023,RMVar_hsa_circ_184021 112387 RMVar_ID_112387 Human_SNP_ID_828244211 m1A Human chr17 + 80107592 80107592 80107592 GAACACGACGGTGGCGCCCCTGTTCTTTGCGGACCAGTTCCTTCAGCTGTCCACCTCGCTGCCCT GAACACGACGGTGGCGCCCCTGTTCTTTGCGGGCCAGTTCCTTCAGCTGTCCACCTCGCTGCCCT A G GAA Ensembl:ENSG00000171298 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:80104941..80107666 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_Splice_Rec_1877372,Human_Splice_Rec_1877378,Human_Splice_Rec_1877422 RMVar_hsa_circ_9198,RMVar_hsa_circ_64421 112388 RMVar_ID_112388 Human_SNP_ID_828246124 m1A Human chr17 - 82053365 82053365 82053365 ACACCCAAGGTCCCCCCACTGGGCTCCGTACCAGGCTGGGGTTCTCCACCACGTAGTTGACGTCA ACACCCAAGGTCCCCCCACTGGGCTCCGTACCGGGCTGGGGTTCTCCACCACGTAGTTGACGTCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:82053252..82053402 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 112389 RMVar_ID_112389 Human_SNP_ID_828247347 m1A Human chr17 - 7675149 7675149 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGCCCCCGCGTCCGCGCCATGGCCATCTACAAGCAG T G TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,nasopharynx non_keratinizing_non_differentiated,pancreas ductal_carcinoma,mouth squamous_cell_carcinoma,lung adenocarcinoma,oesophagus squamous_cell_carcinoma,oesophagus adenocarcinoma,ESCA,LGG,BRCA,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,LUSC,head_neck squamous_cell_carcinoma,pharynx nasopharyngeal_carcinoma,lung small_cell_carcinoma 462 lung,oesophagus,pancreas,head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112390 RMVar_ID_112390 Human_SNP_ID_828247351 m1A Human chr17 - 7675149 7675149 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGCGCCCGCGTCCGCGCCATGGCCATCTACAAGCAG T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) rs772683278 Functional Loss SNV COSMIC 33..33 33 brain astrocytoma_Grade_III,rectum adenocarcinoma,central_nervous_system astrocytoma_Grade_III,oesophagus adenocarcinoma,lung adenocarcinoma,lung bronchioloalveolar_adenocarcinoma,bone ameloblastoma,ovary serous_carcinoma,large_intestine adenocarcinoma 133 lung,ovary,oesophagus,bone,large intestine,brain Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 Clinvar_Rec_657 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112391 RMVar_ID_112391 Human_SNP_ID_828248357 m1A Human chr17 + 16353180 16353180 16353180 CGGGAGTCGGCGGCGGCGGCGGCGGTGGCGGGAGCAACGCCAGCTCAGGCGGCGGCGGCTCCCCC CGGGAGTCGGCGGCGGCGGCGGCGGTGGCGGGGGCAACGCCAGCTCAGGCGGCGGCGGCTCCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16353091..16353429 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112392 RMVar_ID_112392 Human_SNP_ID_828252800 m1A Human chr17 + 20205101 20205101 20205101 AAGGCCCCTGTCCTCCACCAGTAACCCCTTTAAGAGTTCAAAGTGTTCTACTGCTGGGAGTTCCC AAGGCCCCTGTCCTCCACCAGTAACCCCTTTAGGAGTTCAAAGTGTTCTACTGCTGGGAGTTCCC A G SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:20205076..20205100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 8 liver Human_RBP_ID_46478,Human_RBP_ID_3548243,Human_RBP_ID_5098131 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182685,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_182689,RMVar_hsa_circ_312205,RMVar_hsa_circ_330276,RMVar_hsa_circ_340270,RMVar_hsa_circ_337476,RMVar_hsa_circ_326157,RMVar_hsa_circ_294190,RMVar_hsa_circ_302130,RMVar_hsa_circ_271270,RMVar_hsa_circ_182687,RMVar_hsa_circ_182688,RMVar_hsa_circ_182686,RMVar_hsa_circ_182684 112393 RMVar_ID_112393 Human_SNP_ID_828254237 m1A Human chr17 + 3680298 3680298 3680298 ACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGCAT ACCCAGTGTCCTCCACCCTGCATCCTCCACCCTGTGTCCTCCACCCTGCATCCTCCACCCTGCAT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3680294..3680727 26863196 MeRIP-seq:(Medium) rs374033661 Functional Loss SNV ICGC 33..33 33 LUSC 2 - 112394 RMVar_ID_112394 Human_SNP_ID_828265312 m1A Human chr17 - 31008646 31008646 31008646 TCAGGGGCTGAGGCCCGAGCTTTTGGCGCTGCAACCGCCACGGCCGGAGGGTCCCGGACGTGCCG TCAGGGGCTGAGGCCCGAGCTTTTGGCGCTGCGACCGCCACGGCCGGAGGGTCCCGGACGTGCCG T C lnc-TEFM-8 RNACentral:URS00008C0AFF lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:31008546..31008647 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112395 RMVar_ID_112395 Human_SNP_ID_828266106 m1A Human chr17 + 44351655 44351655 44351655 AACAGGGGCCCCACCAGGTGCCCTGGATGGAGAAGGCCCCAGCTCACCTCAGCCTGCCAGACCCA AACAGGGGCCCCACCAGGTGCCCTGGATGGAGGAGGCCCCAGCTCACCTCAGCCTGCCAGACCCA A G GRN Ensembl:ENSG00000030582 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:44351604..44351793;chr17:44351605..44351732 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 3 head and neck Human_RBP_ID_235624,Human_RBP_ID_764339,Human_RBP_ID_903475,Human_RBP_ID_5115176,Human_RBP_ID_22443734,Human_RBP_ID_22761567 Human_miRNA_ID_2685817 RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_6271,RMVar_hsa_circ_106530,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691,RMVar_hsa_circ_184692,RMVar_hsa_circ_94458,RMVar_hsa_circ_269494,RMVar_hsa_circ_184694,RMVar_hsa_circ_77417,RMVar_hsa_circ_184695 112396 RMVar_ID_112396 Human_SNP_ID_828268541 m1A Human chr17 - 4968362 4968362 4968362 CGCCTCGGTTCCCACCACTGCCTTCGCTGCGCACGCCCCTCGTGTTTCAGGGCTGACCGTGTCCC CGCCTCGGTTCCCACCACTGCCTTCGCTGCGCGCGCCCCTCGTGTTTCAGGGCTGACCGTGTCCC T C CAMTA2 Ensembl:ENSG00000108509 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:4968252..4968725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 11 pancreas Human_RBP_ID_493444,Human_RBP_ID_18942709,Human_RBP_ID_21974094,Human_RBP_ID_22370696 Human_miRNA_ID_175421,Human_miRNA_ID_1807898 112397 RMVar_ID_112397 Human_SNP_ID_828268733 m1A Human chr17 + 4789664 4789664 4789664 ATGTGGGGCTGTCGCCGTACCTGGCGGGATGGAGGGCACTCGTCGAGTGAGTGGCCTCCCGCCCC ATGTGGGGCTGTCGCCGTACCTGGCGGGATGGTGGGCACTCGTCGAGTGAGTGGCCTCCCGCCCC A T GLTPD2 Ensembl:ENSG00000182327 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:4789627..4789777 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 1 ovary Human_RBP_ID_18990111,Human_RBP_ID_22415853,Human_RBP_ID_22443351,Human_RBP_ID_22657282 Human_Splice_Rec_1764479 112398 RMVar_ID_112398 Human_SNP_ID_828271310 m1A Human chr17 - 81552257 81552257 81552257 CTGCTGCCCTCTCGGGGGCCTGGCGGCGGGCAAGCCCCGCGTGCTGTGCCATGAGGCAGAGGTCT CTGCTGCCCTCTCGGGGGCCTGGCGGCGGGCATGCCCCGCGTGCTGTGCCATGAGGCAGAGGTCT T A FAAP100 Ensembl:ENSG00000185504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81552211..81552333 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 2 - Human_RBP_ID_4464898 Human_Splice_Rec_1881095,Human_Splice_Rec_1881115 112399 RMVar_ID_112399 Human_SNP_ID_828273274 m1A Human chr17 - 1050099 1050099 1050099 TGAGAAGTGCTATGACAAGACCAAGGTCAACAAGGACAACAATGAGATCGTGGACAAGATCATGG TGAGAAGTGCTATGACAAGACCAAGGTCAACACGGACAACAATGAGATCGTGGACAAGATCATGG T G ABR Ensembl:ENSG00000159842 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1050008..1050116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 7 uterus Human_RBP_ID_1872251,Human_RBP_ID_18531024 Human_Splice_Rec_1756746,Human_Splice_Rec_1756747,Human_Splice_Rec_1756798,Human_Splice_Rec_1756799,Human_Splice_Rec_1756856,Human_Splice_Rec_1756857,Human_Splice_Rec_1756898,Human_Splice_Rec_1756899,Human_Splice_Rec_1756946,Human_Splice_Rec_1756947,Human_Splice_Rec_1757000,Human_Splice_Rec_1757001,Human_Splice_Rec_1757019,Human_Splice_Rec_1757032,Human_Splice_Rec_1757042 Human_miRNA_ID_2255435 RMVar_hsa_circ_50633,RMVar_hsa_circ_91339,RMVar_hsa_circ_180950,RMVar_hsa_circ_180952,RMVar_hsa_circ_110228,RMVar_hsa_circ_334699,RMVar_hsa_circ_336127,RMVar_hsa_circ_372052,RMVar_hsa_circ_299917,RMVar_hsa_circ_180955,RMVar_hsa_circ_180957,RMVar_hsa_circ_22687,RMVar_hsa_circ_180956,RMVar_hsa_circ_180954 112400 RMVar_ID_112400 Human_SNP_ID_828274641 m1A Human chr17 + 81511398 81511398 81511398 GATTTCCCGCTCGGCCGTGGTGGTGAAGCTGTAGCCTCGCTCAGTGAGGATCTTCATGAGGTAGT GATTTCCCGCTCGGCCGTGGTGGTGAAGCTGTCGCCTCGCTCAGTGAGGATCTTCATGAGGTAGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81511230..81511588 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue 112401 RMVar_ID_112401 Human_SNP_ID_828280764 m1A Human chr17 + 7591328 7591328 7591328 CACCAGACAAGGTTGGTCCCCTCCCCAGGGGGACCTTGTCACCCCCCTTCATACACACCCCTGGT CACCAGACAAGGTTGGTCCCCTCCCCAGGGGGGCCTTGTCACCCCCCTTCATACACACCCCTGGT A G MPDU1 Ensembl:ENSG00000129255 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:7591277..7591375;chr17:7591279..7591385 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112402 RMVar_ID_112402 Human_SNP_ID_828282874 m1A Human chr17 - 63830915 63830915 63830915 AGCCATGGTTACCTTCCCCTATGAATTTCTGTACCAGTTCAGAGCCAGAGACACGAATAAAGGTA AGCCATGGTTACCTTCCCCTATGAATTTCTGTTCCAGTTCAGAGCCAGAGACACGAATAAAGGTA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:63830144..63830923 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 pelvis central,BOCA,bone central 5 bone 112403 RMVar_ID_112403 Human_SNP_ID_828283793 m1A Human chr17 + 82056765 82056765 82056765 GCTGATCAGTGCCCGTGTGGACTCACACAGCAAGGTGGCTGTGGGCTGCGGGGCGGTGGGGGCAG GCTGATCAGTGCCCGTGTGGACTCACACAGCAGGGTGGCTGTGGGCTGCGGGGCGGTGGGGGCAG A G GPS1 Ensembl:ENSG00000169727 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82056725..82056825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach Human_RBP_ID_17903238,Human_RBP_ID_19084667 Human_Splice_Rec_1883915,Human_Splice_Rec_1883941,Human_Splice_Rec_1883965,Human_Splice_Rec_1884013,Human_Splice_Rec_1884075,Human_Splice_Rec_1884109,Human_Splice_Rec_1884133,Human_Splice_Rec_1884163,Human_Splice_Rec_1884183,Human_Splice_Rec_1884189,Human_Splice_Rec_1884193 RMVar_hsa_circ_93786,RMVar_hsa_circ_104069,RMVar_hsa_circ_187831,RMVar_hsa_circ_187832,RMVar_hsa_circ_112668,RMVar_hsa_circ_187834,RMVar_hsa_circ_91268,RMVar_hsa_circ_101739,RMVar_hsa_circ_187836,RMVar_hsa_circ_106850,RMVar_hsa_circ_187838,RMVar_hsa_circ_90754,RMVar_hsa_circ_49044,RMVar_hsa_circ_87744,RMVar_hsa_circ_187839,RMVar_hsa_circ_187840,RMVar_hsa_circ_187841,RMVar_hsa_circ_108077,RMVar_hsa_circ_346847,RMVar_hsa_circ_187843,RMVar_hsa_circ_187844 112404 RMVar_ID_112404 Human_SNP_ID_828285275 m1A Human chr17 + 82601375 82601375 82601375 CGCATCGGCCTCCCTGCCCACAAAGCGCCACAACGGTGACCAGCCGGAGCAGCCGGAGCTGAAGC CGCATCGGCCTCCCTGCCCACAAAGCGCCACATCGGTGACCAGCCGGAGCAGCCGGAGCTGAAGC A T FOXK2 Ensembl:ENSG00000141568 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82601326..82601548 26863196 MeRIP-seq:(Medium) rs1050277971 Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 1 breast Human_RBP_ID_13208282 Human_Splice_Rec_1886158,Human_Splice_Rec_1886174,Human_Splice_Rec_1886212,Human_Splice_Rec_1886218 112405 RMVar_ID_112405 Human_SNP_ID_828286234 m1A Human chr17 - 44708732 44708732 44708732 ATTCGCGAGCTCCATGAGCTCTTCCCGATTCCACAGTCCTGGTTATCTCAGGGCAGCTACAGCAT ATTCGCGAGCTCCATGAGCTCTTCCCGATTCCGCAGTCCTGGTTATCTCAGGGCAGCTACAGCAT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:44708713..44708850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112406 RMVar_ID_112406 Human_SNP_ID_828286870 m1A Human chr17 + 28950967 28950967 28950967 GTCTTGGTCTCCATTTTCTCCCACATTCATCCACCTCCCGGGCTGGGTGCTCTCTGCTCCGGCCC GTCTTGGTCTCCATTTTCTCCCACATTCATCCTCCTCCCGGGCTGGGTGCTCTCTGCTCCGGCCC A T PIPOX Ensembl:ENSG00000179761 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:28950918..28951496 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary 112407 RMVar_ID_112407 Human_SNP_ID_828287402 m1A Human chr17 - 29294055 29294055 29294055 CTCAGCCAGGGAGTCCCAGCCGCTTTCAATGGAGGAGAAGCCCGGCCAGCCACAGCCTCAGCACC CTCAGCCAGGGAGTCCCAGCCGCTTTCAATGGCGGAGAAGCCCGGCCAGCCACAGCCTCAGCACC T G NUFIP2 Ensembl:ENSG00000108256 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:29293987..29294072 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_50369,Human_RBP_ID_768155,Human_RBP_ID_4465264,Human_RBP_ID_5259966,Human_RBP_ID_6575114,Human_RBP_ID_9375633,Human_RBP_ID_18419568,Human_RBP_ID_26331516,Human_RBP_ID_26958092 112408 RMVar_ID_112408 Human_SNP_ID_828289860 m1A Human chr17 - 41909070 41909070 41909070 GGATGAACTGTCCCTCTCTCCCTCCCACCTCTAGAATTCTGGCCAGTTTTATCTCCGGCCTCTTC GGATGAACTGTCCCTCTCTCCCTCCCACCTCTCGAATTCTGGCCAGTTTTATCTCCGGCCTCTTC T G ACLY Ensembl:ENSG00000131473 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:41909051..41909075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_8452321 Human_Splice_Rec_1816963,Human_Splice_Rec_1817019,Human_Splice_Rec_1817075,Human_Splice_Rec_1817169,Human_Splice_Rec_1817239 RMVar_hsa_circ_3671,RMVar_hsa_circ_366393,RMVar_hsa_circ_11177,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_113752,RMVar_hsa_circ_35343,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_115959,RMVar_hsa_circ_24463,RMVar_hsa_circ_184247,RMVar_hsa_circ_184248,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_337607,RMVar_hsa_circ_281028,RMVar_hsa_circ_184259,RMVar_hsa_circ_184260,RMVar_hsa_circ_367772,RMVar_hsa_circ_357162,RMVar_hsa_circ_90670,RMVar_hsa_circ_34737,RMVar_hsa_circ_88642,RMVar_hsa_circ_184262,RMVar_hsa_circ_11163,RMVar_hsa_circ_184263,RMVar_hsa_circ_36161 112409 RMVar_ID_112409 Human_SNP_ID_828295880 m1A Human chr17 - 7676594 7676594 7676594 GCAGCAGCCAGACTGCCTTCCGGGTCACTGCCATGGAGGAGCCGCAGTCAGATCCTAGCGTCGAG GCAGCAGCCAGACTGCCTTCCGGGTCACTGCCGTGGAGGAGCCGCAGTCAGATCCTAGCGTCGAG T C TP53 Ensembl:ENSG00000141510 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7676479..7676653 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 15 head and neck Human_RBP_ID_768584,Human_RBP_ID_4466076,Human_RBP_ID_6647593,Human_RBP_ID_9375311,Human_RBP_ID_18709875,Human_RBP_ID_22443450 Human_Splice_Rec_1773739,Human_Splice_Rec_1773752,Human_Splice_Rec_1773753,Human_Splice_Rec_1773773,Human_Splice_Rec_1773870,Human_Splice_Rec_1773888,Human_Splice_Rec_1773889,Human_Splice_Rec_1773908,Human_Splice_Rec_1773909,Human_Splice_Rec_1773928,Human_Splice_Rec_1773929,Human_Splice_Rec_1773950,Human_Splice_Rec_1773951,Human_Splice_Rec_1773972,Human_Splice_Rec_1773973,Human_Splice_Rec_1773994,Human_Splice_Rec_1773995,Human_Splice_Rec_1774016,Human_Splice_Rec_1774017,Human_Splice_Rec_1774038,Human_Splice_Rec_1774039,Human_Splice_Rec_1774058,Human_Splice_Rec_1774059,Human_Splice_Rec_1774079,Human_Splice_Rec_1774106,Human_Splice_Rec_1774107,Human_Splice_Rec_1774118,Human_Splice_Rec_1774126,Human_Splice_Rec_1774127,Human_Splice_Rec_1774134,Human_Splice_Rec_1774135,Human_Splice_Rec_1774144,Human_Splice_Rec_1774145 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 112410 RMVar_ID_112410 Human_SNP_ID_828308633 m1A Human chr17 + 73232249 73232249 73232249 AGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTACCCCTCAGTCGGACCCGTACCACCACTACTTC AGCCGCTCGGGTGGACGCAGCCGGTGGCGAGTTCCCCTCAGTCGGACCCGTACCACCACTACTTC A T C17orf80 Ensembl:ENSG00000141219 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:73232115..73232314 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 112411 RMVar_ID_112411 Human_SNP_ID_828309863 m1A Human chr17 - 44198132 44198132 44198132 ACTCACAACAACACCCCCACCCCCGTGTGTGCAGCCGTGTTGCCGCCCGCTGTGCTATGAGCAGT ACTCACAACAACACCCCCACCCCCGTGTGTGCTGCCGTGTTGCCGCCCGCTGTGCTATGAGCAGT T A ATXN7L3 Ensembl:ENSG00000087152 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:44198026..44198199 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_18459702,Human_RBP_ID_22656397,Human_RBP_ID_26782326 112412 RMVar_ID_112412 Human_SNP_ID_828310008 m1A Human chr17 + 20232213 20232213 20232213 TGGGCTCTGACATTTTCAGGAGGAGACCGAGGAATGGAGGCGGTTCCAGGCGGATCTGCAGACCG TGGGCTCTGACATTTTCAGGAGGAGACCGAGGTATGGAGGCGGTTCCAGGCGGATCTGCAGACCG A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA exon,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:20232201..20232250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_46488,Human_RBP_ID_901349,Human_RBP_ID_3549108,Human_RBP_ID_5579330,Human_RBP_ID_26331389,Human_RBP_ID_27812376 Human_Splice_Rec_1792318,Human_Splice_Rec_1792332,Human_Splice_Rec_1792396,Human_Splice_Rec_1792410,Human_Splice_Rec_1792448,Human_Splice_Rec_1792470,Human_Splice_Rec_1792478,Human_Splice_Rec_1792488,Human_Splice_Rec_1792496,Human_Splice_Rec_1792522 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_182689,RMVar_hsa_circ_330276,RMVar_hsa_circ_340270,RMVar_hsa_circ_326157,RMVar_hsa_circ_294190,RMVar_hsa_circ_302130,RMVar_hsa_circ_182687,RMVar_hsa_circ_182688,RMVar_hsa_circ_182686,RMVar_hsa_circ_182690,RMVar_hsa_circ_11564,RMVar_hsa_circ_305730,RMVar_hsa_circ_371077,RMVar_hsa_circ_316155,RMVar_hsa_circ_293838,RMVar_hsa_circ_182691,RMVar_hsa_circ_182694,RMVar_hsa_circ_182692,RMVar_hsa_circ_287577,RMVar_hsa_circ_300199,RMVar_hsa_circ_182693,RMVar_hsa_circ_99026 112413 RMVar_ID_112413 Human_SNP_ID_828310074 m1A Human chr17 + 7894499 7894499 7894499 GGATCACCAGGATTACTGTGAGGTGTGCCAGCAGGGTGGGGAAATTATTCTGTGTGACACCTGCC GGATCACCAGGATTACTGTGAGGTGTGCCAGCGGGGTGGGGAAATTATTCTGTGTGACACCTGCC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:7894451..7894525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_896177,Human_RBP_ID_1870296,Human_RBP_ID_17902303,Human_RBP_ID_22715666,Human_RBP_ID_26332846 Human_Splice_Rec_1774934,Human_Splice_Rec_1775024,Human_Splice_Rec_1775076,Human_Splice_Rec_1775154,Human_Splice_Rec_1775230,Human_Splice_Rec_1775244,Human_Splice_Rec_1775248 112414 RMVar_ID_112414 Human_SNP_ID_828312554 m1A Human chr17 - 17761561 17761561 17761561 TCAGGGATCACCTCCTCTCAAATCTCACTGTGACTTTCCAACTGATGCCTGCCCTAGATACCCTC TCAGGGATCACCTCCTCTCAAATCTCACTGTGGCTTTCCAACTGATGCCTGCCCTAGATACCCTC T C RAI1-AS1 Ensembl:ENSG00000237328 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17761559..17761977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 112415 RMVar_ID_112415 Human_SNP_ID_828312706 m1A Human chr17 - 50662182 50662182 50662182 GCACACGCCCATCTCCCAAATTGCTCCTGAATACTTGTCTCATTCCTGGCCTGGACTCCATCTGA GCACACGCCCATCTCCCAAATTGCTCCTGAATGCTTGTCTCATTCCTGGCCTGGACTCCATCTGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50661953..50662339 26863196 MeRIP-seq:(Medium) rs7216383 Functional Loss SNV ICGC 33..33 33 LAML 1 - 112416 RMVar_ID_112416 Human_SNP_ID_828317913 m1A Human chr17 - 47840282 47840282 47840282 CTTCTTGGCTATGGGGGGCTGAGATGGGCGCCAACGAGCATGGTGTCTGCATTGGCAACGAGGCT CTTCTTGGCTATGGGGGGCTGAGATGGGCGCCCACGAGCATGGTGTCTGCATTGGCAACGAGGCT T G SCRN2 Ensembl:ENSG00000141295 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47840237..47840318 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_Splice_Rec_1833162,Human_Splice_Rec_1833163,Human_Splice_Rec_1833176,Human_Splice_Rec_1833177,Human_Splice_Rec_1833186,Human_Splice_Rec_1833187,Human_Splice_Rec_1833200,Human_Splice_Rec_1833201,Human_Splice_Rec_1833220,Human_Splice_Rec_1833221,Human_Splice_Rec_1833250,Human_Splice_Rec_1833251,Human_Splice_Rec_1833258,Human_Splice_Rec_1833262 112417 RMVar_ID_112417 Human_SNP_ID_828319743 m1A Human chr17 - 42698780 42698780 42698780 GAGCTTGGTTGGGAGCTGCTGTAGGGGTGGGGACCTGGGCAGGGCCTGAAGTGGGTAGGGGAGGT GAGCTTGGTTGGGAGCTGCTGTAGGGGTGGGGGCCTGGGCAGGGCCTGAAGTGGGTAGGGGAGGT T C AC100793.3 Ensembl:ENSG00000267765 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:42698733..42698825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_200554 112418 RMVar_ID_112418 Human_SNP_ID_828322992 m1A Human chr17 + 17793469 17793469 17793469 GGTGCCCTTTCGGACTCACTCCCTGCACGTCCAGCAGCCACCGCCGCCCCAGCAGCCCCTGGCAT GGTGCCCTTTCGGACTCACTCCCTGCACGTCCGGCAGCCACCGCCGCCCCAGCAGCCCCTGGCAT A G RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:17793419..17793701 26863196 MeRIP-seq:(Medium) rs1053199893 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_27449046 Human_Splice_Rec_1785737 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 112419 RMVar_ID_112419 Human_SNP_ID_828328242 m1A Human chr17 - 16353173 16353164 16353173 CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCCACCGCCGCCGCCGCCGCCGACTCCCGCGACCCC CCGCCGCCGCCTGAGCTGGCGTTGCTCCCGCC_________GCCGCCGCCGACTCCCGCGACCCC CGGCGGCGGT C CENPV Ensembl:ENSG00000166582 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16353126..16353475 26863196 MeRIP-seq:(Medium) rs746979329 Functional Loss DEL ICGC 33..41 33 STAD 1 - Human_RBP_ID_236564,Human_RBP_ID_4407566,Human_RBP_ID_5237867,Human_RBP_ID_22442816 RMVar_hsa_circ_126839,RMVar_hsa_circ_182319 112420 RMVar_ID_112420 Human_SNP_ID_828330892 m1A Human chr17 + 59697977 59697977 59697977 CCAAATATTCCATAACCAAGGATTTGGAGGGCATCTTAAAGGAAAGGAAAACAGTTATCACTATC CCAAATATTCCATAACCAAGGATTTGGAGGGCGTCTTAAAGGAAAGGAAAACAGTTATCACTATC A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:59697808..59698000;chr17:59697729..59697990 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 112421 RMVar_ID_112421 Human_SNP_ID_828331828 m1A Human chr17 - 47808401 47808401 47808401 TTCACCCCTCACTGCCACCGCCTTCTCCCACCAGGCGGCAGACGGATAGCAGCGGGAAAGAGTGG TTCACCCCTCACTGCCACCGCCTTCTCCCACCCGGCGGCAGACGGATAGCAGCGGGAAAGAGTGG T G OSBPL7 Ensembl:ENSG00000006025 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:47808353..47808447 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 112422 RMVar_ID_112422 Human_SNP_ID_828346794 m1A Human chr17 - 72121816 72121816 72121816 GCCGCGCCGCCCCCGCCGGGTCCTACCTCCAGAGCTTGCCCAGCGTCTTGCTGAGCTCGGCGTTG GCCGCGCCGCCCCCGCCGGGTCCTACCTCCAGCGCTTGCCCAGCGTCTTGCTGAGCTCGGCGTTG T G SOX9-AS1 Ensembl:ENSG00000234899 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:72121766..72122834 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 112423 RMVar_ID_112423 Human_SNP_ID_828348783 m1A Human chr17 + 38918897 38918897 38918897 TTTTTTAAAACCTGCGACAGCTTGTGATTCCTACCCCTCTTCCAGCTTCTTTTGCCAACTGAAGC TTTTTTAAAACCTGCGACAGCTTGTGATTCCTGCCCCTCTTCCAGCTTCTTTTGCCAACTGAAGC A G LASP1 Ensembl:ENSG00000002834 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:38918876..38918900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bone osteoblastic,femur osteoblastic 3 bone Human_RBP_ID_2505084,Human_RBP_ID_3521800,Human_RBP_ID_24416420 Human_miRNA_ID_465065,Human_miRNA_ID_1560303,Human_miRNA_ID_2153737,Human_miRNA_ID_2801614,Human_miRNA_ID_3009745 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_125964,RMVar_hsa_circ_183854 112424 RMVar_ID_112424 Human_SNP_ID_828356451 m1A Human chr17 + 63607437 63607437 63607437 GAAGCAGGAGCTGAGGATGTCAAGGAAACTGAAGATGAAGAAGAAAGGAACGTTTTTAAAGTAAG GAAGCAGGAGCTGAGGATGTCAAGGAAACTGATGATGAAGAAGAAAGGAACGTTTTTAAAGTAAG A T TACO1 Ensembl:ENSG00000136463 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63607387..63608020 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_1539828,Human_RBP_ID_1866618,Human_RBP_ID_3533845,Human_RBP_ID_6632087,Human_RBP_ID_19083481,Human_RBP_ID_26332169 Human_Splice_Rec_1852033,Human_Splice_Rec_1852041 RMVar_hsa_circ_113615,RMVar_hsa_circ_186317 112425 RMVar_ID_112425 Human_SNP_ID_828360962 m1A Human chr17 - 38852638 38852619 38852639 GCTGCTGGTGTGGGTGACATGGTGATGGCCACAGTCAAGAAAGGCAAACCAGAGCTCAGAAAAAA GCTGCTGGTGTGGGTGACATGGTGATGGCCA____________________GAGCTCAGAAAAAA CTGGTTTGCCTTTCTTGACTG C RPL23 Ensembl:ENSG00000125691 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38852601..38852750 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..51 33 BLCA 1 - Human_RBP_ID_488227,Human_RBP_ID_902099,Human_RBP_ID_1532882,Human_RBP_ID_1856815,Human_RBP_ID_3521782,Human_RBP_ID_4423096,Human_RBP_ID_6590410,Human_RBP_ID_8451197,Human_RBP_ID_9071677,Human_RBP_ID_9859122,Human_RBP_ID_17262832,Human_RBP_ID_17378295,Human_RBP_ID_17691899,Human_RBP_ID_18696271,Human_RBP_ID_22445417,Human_RBP_ID_22499324,Human_RBP_ID_22804201,Human_RBP_ID_22960739,Human_RBP_ID_23724000,Human_RBP_ID_25278909,Human_RBP_ID_26460477,Human_RBP_ID_26812206,Human_RBP_ID_26959837,Human_RBP_ID_27253257 Human_Splice_Rec_1810180,Human_Splice_Rec_1810181,Human_Splice_Rec_1810188,Human_Splice_Rec_1810189,Human_Splice_Rec_1810198,Human_Splice_Rec_1810199,Human_Splice_Rec_1810206,Human_Splice_Rec_1810207,Human_Splice_Rec_1810214,Human_Splice_Rec_1810218,Human_Splice_Rec_1810219,Human_Splice_Rec_1810224,Human_Splice_Rec_1810225,Human_Splice_Rec_1810230,Human_Splice_Rec_1810231 RMVar_hsa_circ_88309,RMVar_hsa_circ_287277,RMVar_hsa_circ_183843,RMVar_hsa_circ_103813,RMVar_hsa_circ_49615,RMVar_hsa_circ_183845,RMVar_hsa_circ_183846 112426 RMVar_ID_112426 Human_SNP_ID_828370728 m1A Human chr17 + 73269461 73269461 73269461 ACTCACTCACTCATTCACTCACTCATTCTCTCATTCACCCACTCATTCTCTCATTCACTCACTCA ACTCACTCACTCATTCACTCACTCATTCTCTCGTTCACCCACTCATTCTCTCATTCACTCACTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:73269219..73269559 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112427 RMVar_ID_112427 Human_SNP_ID_828374600 m1A Human chr17 + 44967660 44967660 44967660 CGTGGGGGTTCTTGAGGCCGGCGTAGAAGGCCACGCGCGGCACCGTGGTGTAGGTGGCAGTGCTG CGTGGGGGTTCTTGAGGCCGGCGTAGAAGGCCGCGCGCGGCACCGTGGTGTAGGTGGCAGTGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44967615..44967808 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 1 stomach 112428 RMVar_ID_112428 Human_SNP_ID_828374972 m1A Human chr17 - 1361296 1361296 1361296 TTTTTTTTTTTAATTTTGGTTTTGTTTTAGGAAAGGGGACTACCACAGGTATCTGGCAGAATTTG TTTTTTTTTTTAATTTTGGTTTTGTTTTAGGACAGGGGACTACCACAGGTATCTGGCAGAATTTG T G YWHAE Ensembl:ENSG00000108953 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1345370..1361700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_6558706,Human_RBP_ID_12886328,Human_RBP_ID_17904590 Human_Splice_Rec_1757150,Human_Splice_Rec_1757166 RMVar_hsa_circ_30847,RMVar_hsa_circ_273626,RMVar_hsa_circ_93985,RMVar_hsa_circ_338270,RMVar_hsa_circ_180978,RMVar_hsa_circ_292129,RMVar_hsa_circ_180979,RMVar_hsa_circ_180980,RMVar_hsa_circ_270425,RMVar_hsa_circ_277999,RMVar_hsa_circ_96697,RMVar_hsa_circ_180981,RMVar_hsa_circ_180982,RMVar_hsa_circ_180983 112429 RMVar_ID_112429 Human_SNP_ID_828376839 m1A Human chr17 - 81703243 81703243 81703243 GCAGCTAGACATCGGGCGACCCTCGTCCCGCCAGGTTTTGGGGTCGCGCAAACGAGCGACGGGGG GCAGCTAGACATCGGGCGACCCTCGTCCCGCCGGGTTTTGGGGTCGCGCAAACGAGCGACGGGGG T C AC139530.1 Ensembl:ENSG00000262049 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132802 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_4467590 GWAS_ID_13199,GWAS_ID_13200,GWAS_ID_13201,GWAS_ID_13202,GWAS_ID_13203,GWAS_ID_13204,GWAS_ID_13205,GWAS_ID_13206,GWAS_ID_13207,GWAS_ID_13208,GWAS_ID_13209,GWAS_ID_13210,GWAS_ID_13211,GWAS_ID_13212,GWAS_ID_13213,GWAS_ID_13214,GWAS_ID_13215,GWAS_ID_13216,GWAS_ID_13217,GWAS_ID_13218,GWAS_ID_13219,GWAS_ID_13220,GWAS_ID_13221,GWAS_ID_13222,GWAS_ID_13223,GWAS_ID_13224,GWAS_ID_13225,GWAS_ID_13226 112430 RMVar_ID_112430 Human_SNP_ID_828377683 m1A Human chr17 - 50863298 50863298 50863298 TATGGGCTTGGCTTGGGTAGCCAGCAGCAGCCACAGCAACAGCAGCAGCCAGCCCAGCCGCCACC TATGGGCTTGGCTTGGGTAGCCAGCAGCAGCCGCAGCAACAGCAGCAGCCAGCCCAGCCGCCACC T C TOB1 Ensembl:ENSG00000141232 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:50863248..50863369 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_5144258,Human_RBP_ID_17264036,Human_RBP_ID_22061513,Human_RBP_ID_27256780 112431 RMVar_ID_112431 Human_SNP_ID_828382391 m1A Human chr17 - 57974583 57974583 57974583 ATATAGCACACCCTGTCACCATCACATCTCCAATGAATCTACCCACACCTATGACATTAGCCGCC ATATAGCACACCCTGTCACCATCACATCTCCATTGAATCTACCCACACCTATGACATTAGCCGCC T A VEZF1 Ensembl:ENSG00000136451 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:57974533..57974643;chr17:57974533..57974641 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_17079697,Human_RBP_ID_18943430 Human_miRNA_ID_1985361,Human_miRNA_ID_2941001 RMVar_hsa_circ_185608,RMVar_hsa_circ_94437,RMVar_hsa_circ_118601,RMVar_hsa_circ_122526,RMVar_hsa_circ_110383,RMVar_hsa_circ_185610,RMVar_hsa_circ_86600,RMVar_hsa_circ_185611,RMVar_hsa_circ_185609,RMVar_hsa_circ_185607 112432 RMVar_ID_112432 Human_SNP_ID_828385602 m1A Human chr17 - 81512117 81512115 81512118 CCTGCAGGGCGTCATGGTGGGCATGGGCCAGAAGGACTCCTACGTGGGCGACGAGGCCCAGAGCA CCTGCAGGGCGTCATGGTGGGCATGGGCCAG___GACTCCTACGTGGGCGACGAGGCCCAGAGCA CCTT C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81512066..81512600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_49502,Human_RBP_ID_502536,Human_RBP_ID_820951,Human_RBP_ID_897033,Human_RBP_ID_1011056,Human_RBP_ID_1289491,Human_RBP_ID_1544465,Human_RBP_ID_1870707,Human_RBP_ID_4458699,Human_RBP_ID_5362182,Human_RBP_ID_6651185,Human_RBP_ID_8465889,Human_RBP_ID_8823425,Human_RBP_ID_9326949,Human_RBP_ID_17902757,Human_RBP_ID_18191034,Human_RBP_ID_22445081,Human_RBP_ID_22587138,Human_RBP_ID_27156937,Human_RBP_ID_27458746 Human_Splice_Rec_1880950,Human_Splice_Rec_1880960,Human_Splice_Rec_1880968,Human_Splice_Rec_1880978,Human_Splice_Rec_1880996,Human_Splice_Rec_1881006,Human_Splice_Rec_1881018,Human_Splice_Rec_1881028,Human_Splice_Rec_1881040,Human_Splice_Rec_1881054,Human_Splice_Rec_1881060,Human_Splice_Rec_1881066,Human_Splice_Rec_1881072 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_81045,RMVar_hsa_circ_187644,RMVar_hsa_circ_307034 112433 RMVar_ID_112433 Human_SNP_ID_828390309 m1A Human chr17 - 2693998 2693998 2693998 AGGAGGGCTGTGAGCTCATCAATGAGGCCCTGAACCTGTTTAACAACGTCTACGGAGCCATGCAC AGGAGGGCTGTGAGCTCATCAATGAGGCCCTGGACCTGTTTAACAACGTCTACGGAGCCATGCAC T C CLUH Ensembl:ENSG00000132361 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2693952..2694032 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_1851668,Human_RBP_ID_8814658 Human_Splice_Rec_1760200,Human_Splice_Rec_1760201,Human_Splice_Rec_1760246,Human_Splice_Rec_1760247,Human_Splice_Rec_1760294,Human_Splice_Rec_1760295,Human_Splice_Rec_1760342,Human_Splice_Rec_1760343,Human_Splice_Rec_1760388,Human_Splice_Rec_1760389,Human_Splice_Rec_1760407,Human_Splice_Rec_1760420,Human_Splice_Rec_1760421 Human_miRNA_ID_1194388,Human_miRNA_ID_2354172,Human_miRNA_ID_2574480 RMVar_hsa_circ_97722,RMVar_hsa_circ_181278,RMVar_hsa_circ_375860,RMVar_hsa_circ_76172,RMVar_hsa_circ_181279,RMVar_hsa_circ_111665,RMVar_hsa_circ_181281,RMVar_hsa_circ_181282 112434 RMVar_ID_112434 Human_SNP_ID_828391794 m1A Human chr17 + 7419358 7419358 7419358 CCCGGAGGGCCTTGGGCTTGGGCATTTGGGAAAAGAATGATGTCTGGAAGGGCTTAAGGGACACA CCCGGAGGGCCTTGGGCTTGGGCATTTGGGAACAGAATGATGTCTGGAAGGGCTTAAGGGACACA A C NLGN2 Ensembl:ENSG00000169992 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7419328..7419417 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_499537,Human_RBP_ID_5115371,Human_RBP_ID_18296334,Human_RBP_ID_18708392 112435 RMVar_ID_112435 Human_SNP_ID_828394754 m1A Human chr17 - 82870316 82870316 82870316 CTGAGGCTCATAGGCACGCGCGAAGGCCCAGCACACGTAGCAGGCGGCGTCCCTGACGTTGGTGC CTGAGGCTCATAGGCACGCGCGAAGGCCCAGCGCACGTAGCAGGCGGCGTCCCTGACGTTGGTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82870176..82870410 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 2 breast 112436 RMVar_ID_112436 Human_SNP_ID_828396250 m1A Human chr17 - 39462131 39462130 39462132 TTAGAGCTGCCGCCTCCCGATGACGGCTGCAAAGTTCCAGAAGCTCCTCCACTCCCGTCCTTCTT TTAGAGCTGCCGCCTCCCGATGACGGCTGCA__GTTCCAGAAGCTCCTCCACTCCCGTCCTTCTT CTT C lnc-MED1-4 RNACentral:URS0000D59046 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39462081..39462171 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 BRCA 1 - 112437 RMVar_ID_112437 Human_SNP_ID_828396871 m1A Human chr17 - 35142076 35142076 35142076 GCGCGATGTGCAGCGGTTGCTAGTGCAGTTCCAGGATGAGGGCGGGCAGCTGCTGGGTTCCCCGT GCGCGATGTGCAGCGGTTGCTAGTGCAGTTCCGGGATGAGGGCGGGCAGCTGCTGGGTTCCCCGT T C NLE1 Ensembl:ENSG00000073536 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:35142026..35142254 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_487347,Human_RBP_ID_897503,Human_RBP_ID_4419728,Human_RBP_ID_6584335,Human_RBP_ID_18694816 Human_Splice_Rec_1804724,Human_Splice_Rec_1804725,Human_Splice_Rec_1804747,Human_Splice_Rec_1804770,Human_Splice_Rec_1804771,Human_Splice_Rec_1804806,Human_Splice_Rec_1804807,Human_Splice_Rec_1804819,Human_Splice_Rec_1804828,Human_Splice_Rec_1804829 RMVar_hsa_circ_377452 112438 RMVar_ID_112438 Human_SNP_ID_828405719 m1A Human chr17 - 40140575 40140575 40140575 GCACCAGATTCCTCGTCCTCGGTGTCTTGCGAAGCGCGCTGCCGCCGCCGGTCCGCCATCTTACG GCACCAGATTCCTCGTCCTCGGTGTCTTGCGATGCGCGCTGCCGCCGCCGGTCCGCCATCTTACG T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:40140544..40140671 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112439 RMVar_ID_112439 Human_SNP_ID_828411191 m1A Human chr17 + 51260637 51260637 51260637 ACGAATGAAACTGGACCGGAGAACCGGAGCGAAGCCGAAGCGGAAGCCCGGAATGAGGCCGGACT ACGAATGAAACTGGACCGGAGAACCGGAGCGAGGCCGAAGCGGAAGCCCGGAATGAGGCCGGACT A G UTP18 Ensembl:ENSG00000011260 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51260514..51266214 26863196 MeRIP-seq:(Medium) rs367594840 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_764301,Human_RBP_ID_3528461,Human_RBP_ID_4465547,Human_RBP_ID_9289242,Human_RBP_ID_9376395,Human_RBP_ID_22445613,Human_RBP_ID_26330806,Human_RBP_ID_27812917 RMVar_hsa_circ_98835,RMVar_hsa_circ_185473 112440 RMVar_ID_112440 Human_SNP_ID_828412929 m1A Human chr17 + 42980610 42980610 42980610 TGGCGGCTGTCGAAGCGGCTGCAGAGCCGGTAACGGTGGTGGCGGCTGTTGGGCCAAAGGCGAAA TGGCGGCTGTCGAAGCGGCTGCAGAGCCGGTAGCGGTGGTGGCGGCTGTTGGGCCAAAGGCGAAA A G RUNDC1 Ensembl:ENSG00000198863 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42980551..42980862 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5441468,Human_RBP_ID_18419612 Human_miRNA_ID_3010896 RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 112441 RMVar_ID_112441 Human_SNP_ID_828412936 m1A Human chr17 + 42980610 42980610 42980610 TGGCGGCTGTCGAAGCGGCTGCAGAGCCGGTAACGGTGGTGGCGGCTGTTGGGCCAAAGGCGAAA TGGCGGCTGTCGAAGCGGCTGCAGAGCCGGTATCGGTGGTGGCGGCTGTTGGGCCAAAGGCGAAA A T RUNDC1 Ensembl:ENSG00000198863 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42980551..42980862 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_5441468,Human_RBP_ID_18419612 Human_miRNA_ID_3010896 RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 112442 RMVar_ID_112442 Human_SNP_ID_828430232 m1A Human chr17 - 81667836 81667836 81667836 ACACACCTGCTTTCTTCCTCTTCTTGTTACTGATCGGGTTTTTCATCTCTTGGCGGCTCCTCATA ACACACCTGCTTTCTTCCTCTTCTTGTTACTGCTCGGGTTTTTCATCTCTTGGCGGCTCCTCATA T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81667670..81667908 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112443 RMVar_ID_112443 Human_SNP_ID_828434877 m1A Human chr17 - 48943962 48943962 48943962 TGGTCTCTTTGTCTGACAGGCCAAGTATAAGGAGCGAGGGACGGTCTTGGCTGAGGACCAGCTAG TGGTCTCTTTGTCTGACAGGCCAAGTATAAGGCGCGAGGGACGGTCTTGGCTGAGGACCAGCTAG T G SNF8 Ensembl:ENSG00000159210 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:48943926..48944000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_48701,Human_RBP_ID_236508,Human_RBP_ID_821980,Human_RBP_ID_905401,Human_RBP_ID_4466554,Human_RBP_ID_8232411,Human_RBP_ID_9376297,Human_RBP_ID_17654800,Human_RBP_ID_22959235 Human_Splice_Rec_1835158,Human_Splice_Rec_1835159,Human_Splice_Rec_1835172,Human_Splice_Rec_1835173,Human_Splice_Rec_1835180,Human_Splice_Rec_1835181,Human_Splice_Rec_1835196,Human_Splice_Rec_1835197,Human_Splice_Rec_1835232,Human_Splice_Rec_1835233,Human_Splice_Rec_1835240,Human_Splice_Rec_1835241,Human_Splice_Rec_1835252,Human_Splice_Rec_1835253,Human_Splice_Rec_1835268,Human_Splice_Rec_1835269,Human_Splice_Rec_1835280,Human_Splice_Rec_1835281,Human_Splice_Rec_1835291,Human_Splice_Rec_1835296,Human_Splice_Rec_1835297 RMVar_hsa_circ_91459,RMVar_hsa_circ_307842,RMVar_hsa_circ_185121,RMVar_hsa_circ_185122 112444 RMVar_ID_112444 Human_SNP_ID_828435539 m1A Human chr17 - 4944982 4944982 4944982 AGACCAGGATAACAGGGGAAGAGGGAGGGGACAGTGGGGGATCTGTTGAAGGCCCAGGAAAAACA AGACCAGGATAACAGGGGAAGAGGGAGGGGACGGTGGGGGATCTGTTGAAGGCCCAGGAAAAACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4944932..4945071 26863196 MeRIP-seq:(Medium) rs1395935097 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 7 kidney 112445 RMVar_ID_112445 Human_SNP_ID_828439005 m1A Human chr17 + 81572075 81572075 81572075 GGGGCCGGGCCAGCTGGGTGATCTCGTTGCCAAACTTGTCTACGTCCTGCAATAGTCAGAGGGGA GGGGCCGGGCCAGCTGGGTGATCTCGTTGCCAGACTTGTCTACGTCCTGCAATAGTCAGAGGGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81572026..81572131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 2 skin,head and neck 112446 RMVar_ID_112446 Human_SNP_ID_828440710 m1A Human chr17 + 1651476 1651476 1651476 TCCCAAGATGGGTTGTCAGCCATGATCTTGGCATGGGTGGTGACATCCTGGGGTGATAACTGCGG TCCCAAGATGGGTTGTCAGCCATGATCTTGGCGTGGGTGGTGACATCCTGGGGTGATAACTGCGG A G NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1651451..1651475 26863196 MeRIP-seq:(Medium) rs1802491 Functional Loss SNV ICGC 33..33 33 COCA 2 - Clinvar_Rec_644 GWAS_ID_13445,GWAS_ID_13446,GWAS_ID_13447,GWAS_ID_13448 112447 RMVar_ID_112447 Human_SNP_ID_828447104 m1A Human chr17 - 50145247 50145247 50145247 GCCGGCCTCTCTGACCAGCTGCCTCCCTCCCCAGGTGTTCAGCACTTACTCCAACGAGGATTACG GCCGGCCTCTCTGACCAGCTGCCTCCCTCCCCGGGTGTTCAGCACTTACTCCAACGAGGATTACG T C PPP1R9B Ensembl:ENSG00000108819 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:50145201..50145250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 112448 RMVar_ID_112448 Human_SNP_ID_828447275 m1A Human chr17 - 74440078 74440078 74440078 CGGGCTTCACCACACAGGCAAACACGAGGCAGAAGAGGCCCAGGGTCCCCAGAAGGAAGAATACC CGGGCTTCACCACACAGGCAAACACGAGGCAGCAGAGGCCCAGGGTCCCCAGAAGGAAGAATACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:74440028..74440178 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112449 RMVar_ID_112449 Human_SNP_ID_828447901 m1A Human chr17 - 49611400 49611400 49611400 ACATTTCTGGCCAGAATACCATGAACATGGTAAAGGTTCCTGAGTGCCGGCTGGCAGATGAGTTA ACATTTCTGGCCAGAATACCATGAACATGGTAGAGGTTCCTGAGTGCCGGCTGGCAGATGAGTTA T C SPOP Ensembl:ENSG00000121067 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49607239..49612811 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_18701562,Human_RBP_ID_23733340 Human_Splice_Rec_1835908,Human_Splice_Rec_1835928,Human_Splice_Rec_1835948,Human_Splice_Rec_1835972,Human_Splice_Rec_1835996,Human_Splice_Rec_1836018,Human_Splice_Rec_1836040,Human_Splice_Rec_1836062,Human_Splice_Rec_1836082,Human_Splice_Rec_1836102,Human_Splice_Rec_1836126,Human_Splice_Rec_1836142,Human_Splice_Rec_1836156,Human_Splice_Rec_1836170 Human_miRNA_ID_1507822 RMVar_hsa_circ_58163,RMVar_hsa_circ_316531,RMVar_hsa_circ_63347,RMVar_hsa_circ_27091,RMVar_hsa_circ_47181,RMVar_hsa_circ_53856,RMVar_hsa_circ_320150 112450 RMVar_ID_112450 Human_SNP_ID_828448280 m1A Human chr17 + 76736431 76736431 76736431 CGAGATCGGCTGCGAGACCTGGAACGACTCCGACTCCGGGATCGGCTGCGGCGACGCCGCCTAGG CGAGATCGGCTGCGAGACCTGGAACGACTCCGTCTCCGGGATCGGCTGCGGCGACGCCGCCTAGG A T AC005837.2,MFSD11 Ensembl:ENSG00000267168,Ensembl:ENSG00000092931 Protein coding,Protein coding intron,5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:76736255..76736975 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 testis seminoma 6 testis RMVar_hsa_circ_187248 112451 RMVar_ID_112451 Human_SNP_ID_828449549 m1A Human chr17 + 45148599 45148595 45148600 GGAGGAAAAGAGGAGGAGGCGGAGGAGAACTGAGCAGAGCAGAGCATCGAGCCAAAGGGGAGATG GGAGGAAAAGAGGAGGAGGCGGAGGAGAA_____CAGAGCAGAGCATCGAGCCAAAGGGGAGATG ACTGAG A HEXIM1 Ensembl:ENSG00000186834 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45148476..45148936 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..34 33 STAD 1 - Human_RBP_ID_897672,Human_RBP_ID_1546657,Human_RBP_ID_3541722,Human_RBP_ID_3950754,Human_RBP_ID_4464617,Human_RBP_ID_5088254,Human_RBP_ID_5143256,Human_RBP_ID_6600910,Human_RBP_ID_8192041,Human_RBP_ID_8232026,Human_RBP_ID_8941826,Human_RBP_ID_9422360,Human_RBP_ID_17653859,Human_RBP_ID_17669960,Human_RBP_ID_18419629,Human_RBP_ID_18544410,Human_RBP_ID_18941780,Human_RBP_ID_22061419,Human_RBP_ID_22357302,Human_RBP_ID_22523793,Human_RBP_ID_22717441,Human_RBP_ID_23118764,Human_RBP_ID_24545021,Human_RBP_ID_24552303,Human_RBP_ID_26331957,Human_RBP_ID_26769319,Human_RBP_ID_27812787 112452 RMVar_ID_112452 Human_SNP_ID_828450989 m1A Human chr17 - 43400234 43400234 43400234 CTGCTGCAGGCCCAGACCGTCCACAGCGCTGCAGCCTTGCACATGAGTGAGAGTGGCGGCTGCTA CTGCTGCAGGCCCAGACCGTCCACAGCGCTGCGGCCTTGCACATGAGTGAGAGTGGCGGCTGCTA T C lnc-LINC00854-1-001 RNACentral:URS00009C15C1 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43400183..43400337 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ACC 1 - 112453 RMVar_ID_112453 Human_SNP_ID_828452909 m1A Human chr17 - 7314551 7314543 7314551 GATAAGATGATGGAACAGAAGATGAAGGAAGAACAGGAGAGAAGGAAGAAAAAGGAGATGGAAGA GATAAGATGATGGAACAGAAGATGAAGGAAGA________GAAGGAAGAAAAAGGAGATGGAAGA CTCTCCTGT C GPS2,AC026954.2 Ensembl:ENSG00000132522,Ensembl:ENSG00000261915 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7314276..7315375 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..40 33 BRCA 1 - Human_RBP_ID_236214,Human_RBP_ID_898230,Human_RBP_ID_1546629,Human_RBP_ID_2522226,Human_RBP_ID_4449200,Human_RBP_ID_5648794,Human_RBP_ID_18987825,Human_RBP_ID_22959346,Human_RBP_ID_24544974,Human_RBP_ID_27812226 Human_Splice_Rec_1771124,Human_Splice_Rec_1771125,Human_Splice_Rec_1771146,Human_Splice_Rec_1771147,Human_Splice_Rec_1771163,Human_Splice_Rec_1771188,Human_Splice_Rec_1771189,Human_Splice_Rec_1771210,Human_Splice_Rec_1771211,Human_Splice_Rec_1771229,Human_Splice_Rec_1771244,Human_Splice_Rec_1771245,Human_Splice_Rec_1771260,Human_Splice_Rec_1771261,Human_Splice_Rec_1771270,Human_Splice_Rec_1771271,Human_Splice_Rec_1771280,Human_Splice_Rec_1771281,Human_Splice_Rec_1771287,Human_Splice_Rec_1771293,Human_Splice_Rec_1771300,Human_Splice_Rec_1771301,Human_Splice_Rec_1771322,Human_Splice_Rec_1771323,Human_Splice_Rec_1771358,Human_Splice_Rec_1771359 RMVar_hsa_circ_6806,RMVar_hsa_circ_105419,RMVar_hsa_circ_125684,RMVar_hsa_circ_98644,RMVar_hsa_circ_181793,RMVar_hsa_circ_101835,RMVar_hsa_circ_181794,RMVar_hsa_circ_181792,RMVar_hsa_circ_345191,RMVar_hsa_circ_87846,RMVar_hsa_circ_307225,RMVar_hsa_circ_181795,RMVar_hsa_circ_181799,RMVar_hsa_circ_83586,RMVar_hsa_circ_368654,RMVar_hsa_circ_181802,RMVar_hsa_circ_359313 112454 RMVar_ID_112454 Human_SNP_ID_828456779 m1A Human chr17 - 61962970 61962970 61962970 CTTTTTGTCTCATTTCTACCTTAAATTTTAGCACGATGGATCGGGATAAAGTGGGAATCCCCACA CTTTTTGTCTCATTTCTACCTTAAATTTTAGCCCGATGGATCGGGATAAAGTGGGAATCCCCACA T G MED13 Ensembl:ENSG00000108510 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:61962934..61963019 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney Human_RBP_ID_25335802 Human_Splice_Rec_1850220 RMVar_hsa_circ_93498,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_330876,RMVar_hsa_circ_267412,RMVar_hsa_circ_102993,RMVar_hsa_circ_186112,RMVar_hsa_circ_186114,RMVar_hsa_circ_186115,RMVar_hsa_circ_186113,RMVar_hsa_circ_309704,RMVar_hsa_circ_266489,RMVar_hsa_circ_59507,RMVar_hsa_circ_119612,RMVar_hsa_circ_127260,RMVar_hsa_circ_369353,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186121,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_186120,RMVar_hsa_circ_303335,RMVar_hsa_circ_56064,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_347960,RMVar_hsa_circ_186126,RMVar_hsa_circ_281878,RMVar_hsa_circ_295627,RMVar_hsa_circ_83249,RMVar_hsa_circ_92610,RMVar_hsa_circ_186128,RMVar_hsa_circ_186130,RMVar_hsa_circ_10329,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_309074,RMVar_hsa_circ_186131,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133 112455 RMVar_ID_112455 Human_SNP_ID_828460191 m1A Human chr17 + 48051399 48051399 48051399 CCTCAGTCAGGTGAGGGCCCTGGACAGGTTCCAGGTGCCAACCACTGAGGTAAATGCCTGGCTGG CCTCAGTCAGGTGAGGGCCCTGGACAGGTTCCGGGTGCCAACCACTGAGGTAAATGCCTGGCTGG A G NFE2L1 Ensembl:ENSG00000082641 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48051201..48051575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung Human_RBP_ID_1008753,Human_RBP_ID_1536015,Human_RBP_ID_8824803,Human_RBP_ID_9073047,Human_RBP_ID_17894570,Human_RBP_ID_22760846 RMVar_hsa_circ_71241,RMVar_hsa_circ_350476 112456 RMVar_ID_112456 Human_SNP_ID_828463362 m1A Human chr17 - 42573482 42573480 42573482 AGCTACCAATCATGTGACTCCAGAAGAGAAAGAGCAGGTGAGCTGGAAGGCTGTAGGACCGCTGT AGCTACCAATCATGTGACTCCAGAAGAGAAAG__CAGGTGAGCTGGAAGGCTGTAGGACCGCTGT GCT G PSMC3IP Ensembl:ENSG00000131470 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:42573006..42573618 26863196 MeRIP-seq:(Medium) rs765972932 Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_3952439,Human_RBP_ID_6595692,Human_RBP_ID_13009627,Human_RBP_ID_18991357,Human_RBP_ID_26333373 Human_Splice_Rec_1819891,Human_Splice_Rec_1819905,Human_Splice_Rec_1819917,Human_Splice_Rec_1819933,Human_Splice_Rec_1819945,Human_Splice_Rec_1819957,Human_Splice_Rec_1819971,Human_Splice_Rec_1819985 112457 RMVar_ID_112457 Human_SNP_ID_828465396 m1A Human chr17 + 35605648 35605648 35605648 ACTGTTAGTTAAGGCTATTCATGTTCTGTCCAACAGCTTGGCACCAACACCTGCTTACTTTCCTT ACTGTTAGTTAAGGCTATTCATGTTCTGTCCAGCAGCTTGGCACCAACACCTGCTTACTTTCCTT A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:35605644..35605731 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_183658,RMVar_hsa_circ_311341,RMVar_hsa_circ_312410 112458 RMVar_ID_112458 Human_SNP_ID_828467466 m1A Human chr17 + 74210367 74210367 74210367 AAATAGCACGTGGGGTTAAACATAACTGGCAGATGTGGGAGCGATGGTGGGGCATGCCATTCAAA AAATAGCACGTGGGGTTAAACATAACTGGCAGGTGTGGGAGCGATGGTGGGGCATGCCATTCAAA A G RPL38 Ensembl:ENSG00000172809 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:74210326..74210463 26863196 MeRIP-seq:(Medium) rs752021453 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_499103,Human_RBP_ID_1010357,Human_RBP_ID_2528628,Human_RBP_ID_6642064,Human_RBP_ID_13155441,Human_RBP_ID_17900403,Human_RBP_ID_27669388 112459 RMVar_ID_112459 Human_SNP_ID_828476132 m1A Human chr17 + 51282511 51282507 51282511 GGAAGGGAGGGAGGGAAGGAAGGAAAGATGGAAGGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA GGAAGGGAGGGAGGGAAGGAAGGAAAGAT____GGAAGGAAGGAAGGAAAGAAAGAAAGAAAGAA TGGAA T UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51282461..51282625 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 ESCA 1 - RMVar_hsa_circ_25562,RMVar_hsa_circ_185475,RMVar_hsa_circ_369667,RMVar_hsa_circ_301462,RMVar_hsa_circ_281866,RMVar_hsa_circ_185476,RMVar_hsa_circ_125773,RMVar_hsa_circ_185474,RMVar_hsa_circ_272858,RMVar_hsa_circ_185484,RMVar_hsa_circ_365891,RMVar_hsa_circ_120638,RMVar_hsa_circ_185486,RMVar_hsa_circ_334960,RMVar_hsa_circ_185485,RMVar_hsa_circ_333354,RMVar_hsa_circ_57920,RMVar_hsa_circ_185488,RMVar_hsa_circ_185489,RMVar_hsa_circ_123397,RMVar_hsa_circ_86134,RMVar_hsa_circ_346876,RMVar_hsa_circ_185490 112460 RMVar_ID_112460 Human_SNP_ID_828477048 m1A Human chr17 + 44148179 44148179 44148179 GAAGAGTGACAGTGACAGAAGTGCTCAGAGAGACAGCAAGACCTCAGTCCTCAGCCTTACACCCC GAAGAGTGACAGTGACAGAAGTGCTCAGAGAGCCAGCAAGACCTCAGTCCTCAGCCTTACACCCC A C HROB Ensembl:ENSG00000125319 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs227584 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_miRNA_ID_1265074,Human_miRNA_ID_2611674 GWAS_ID_15230,GWAS_ID_15231,GWAS_ID_15232,GWAS_ID_15233,GWAS_ID_15234,GWAS_ID_15235,GWAS_ID_15236,GWAS_ID_15237,GWAS_ID_15238,GWAS_ID_15239,GWAS_ID_15240,GWAS_ID_15241,GWAS_ID_15242,GWAS_ID_15243,GWAS_ID_15244,GWAS_ID_15245,GWAS_ID_15246,GWAS_ID_15247,GWAS_ID_15248,GWAS_ID_15249,GWAS_ID_15250,GWAS_ID_15251,GWAS_ID_15252 RMVar_hsa_circ_184642,RMVar_hsa_circ_8262,RMVar_hsa_circ_312362,RMVar_hsa_circ_286468 112461 RMVar_ID_112461 Human_SNP_ID_828477592 m1A Human chr17 + 42422853 42422853 42422853 GCTCGCCCTGGATGCTCTGCACTGCGCCCTCCATCTCCGCCTGCCGCTCCTCCAGCTGTGCTTGA GCTCGCCCTGGATGCTCTGCACTGCGCCCTCCTTCTCCGCCTGCCGCTCCTCCAGCTGTGCTTGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42422605..42422994 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 112462 RMVar_ID_112462 Human_SNP_ID_828478277 m1A Human chr17 + 81512315 81512315 81512315 GTCCCCAGCAAAACCAGCTTTGCACATGCCGGAGCCATTGTCAATGACCAGCGCGGCGATCTCTT GTCCCCAGCAAAACCAGCTTTGCACATGCCGGTGCCATTGTCAATGACCAGCGCGGCGATCTCTT A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:81511912..81512401 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate 112463 RMVar_ID_112463 Human_SNP_ID_828482512 m1A Human chr17 - 18100357 18100357 18100357 GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGAAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC GACTCCAGCTCCTTCTCCAGCAGAGACCTAGGCAGAGTACCCCTTAAGCCCCTCACAGGCTGTCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18100351..18100450 32194978 MeRIP-seq:(Medium) rs2272570 Functional Loss SNV ICGC 33..33 33 COCA 5 - GWAS_ID_7263,GWAS_ID_7264,GWAS_ID_7265,GWAS_ID_7266,GWAS_ID_7267,GWAS_ID_7268,GWAS_ID_7269,GWAS_ID_7270,GWAS_ID_7271,GWAS_ID_7272,GWAS_ID_7273,GWAS_ID_7274,GWAS_ID_7275,GWAS_ID_7276,GWAS_ID_7277,GWAS_ID_7278,GWAS_ID_7279,GWAS_ID_7280,GWAS_ID_7281,GWAS_ID_7282,GWAS_ID_7283,GWAS_ID_7284,GWAS_ID_7285,GWAS_ID_7286,GWAS_ID_7287,GWAS_ID_7288,GWAS_ID_7289,GWAS_ID_7290,GWAS_ID_7291,GWAS_ID_7292,GWAS_ID_7293,GWAS_ID_7294,GWAS_ID_7295,GWAS_ID_7296 112464 RMVar_ID_112464 Human_SNP_ID_828484217 m1A Human chr17 + 44209458 44209458 44209458 GGCTCTGGGAGATGCGCTGCCAGCGACTGCCGATCTCCACCATGCGCTCCTTCAGCGGCAGGTGG GGCTCTGGGAGATGCGCTGCCAGCGACTGCCGGTCTCCACCATGCGCTCCTTCAGCGGCAGGTGG A G AC004596.1 Ensembl:ENSG00000267394 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:44209335..44209470 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 8 kidney 112465 RMVar_ID_112465 Human_SNP_ID_828489301 m1A Human chr17 + 7354761 7354760 7354762 ATAGCTGGGGAAGGCCCAAGGCCGCCCAGGGCAGAGAGAGGAGACGAAGAGTTTGGGACAGTGGG ATAGCTGGGGAAGGCCCAAGGCCGCCCAGGGC__AGAGAGGAGACGAAGAGTTTGGGACAGTGGG CAG C KCTD11 Ensembl:ENSG00000213859 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7352826..7354860 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 COAD 1 - 112466 RMVar_ID_112466 Human_SNP_ID_828491115 m1A Human chr17 + 44349227 44349227 44349227 ACAGCAGGGCTGGTGGCTGGAACGCGGTGCCCAGATGGTCAGTTCTGCCCTGTGGCCTGCTGCCT ACAGCAGGGCTGGTGGCTGGAACGCGGTGCCCTGATGGTCAGTTCTGCCCTGTGGCCTGCTGCCT A T GRN Ensembl:ENSG00000030582 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44349176..44349325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_764334,Human_RBP_ID_903463,Human_RBP_ID_4464607,Human_RBP_ID_5318424,Human_RBP_ID_9289175,Human_RBP_ID_22443725,Human_RBP_ID_23210401 Human_Splice_Rec_1825996,Human_Splice_Rec_1825997,Human_Splice_Rec_1826004,Human_Splice_Rec_1826005,Human_Splice_Rec_1826010,Human_Splice_Rec_1826011,Human_Splice_Rec_1826016,Human_Splice_Rec_1826017,Human_Splice_Rec_1826024,Human_Splice_Rec_1826025,Human_Splice_Rec_1826038,Human_Splice_Rec_1826039,Human_Splice_Rec_1826048,Human_Splice_Rec_1826050,Human_Splice_Rec_1826056,Human_Splice_Rec_1826057,Human_Splice_Rec_1826066,Human_Splice_Rec_1826067,Human_Splice_Rec_1826074,Human_Splice_Rec_1826075,Human_Splice_Rec_1826084,Human_Splice_Rec_1826085,Human_Splice_Rec_1826094,Human_Splice_Rec_1826095,Human_Splice_Rec_1826118,Human_Splice_Rec_1826119,Human_Splice_Rec_1826134,Human_Splice_Rec_1826135,Human_Splice_Rec_1826138,Human_Splice_Rec_1826139,Human_Splice_Rec_1826151 RMVar_hsa_circ_31652,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_184686 112467 RMVar_ID_112467 Human_SNP_ID_828493005 m1A Human chr17 - 8143826 8143826 8143826 CACCCCCAAGCCGCCGACACCACTGCCGATCCAAAGCCAAGCGCTCACGCCACCACCAGAACCCT CACCCCCAAGCCGCCGACACCACTGCCGATCCGAAGCCAAGCGCTCACGCCACCACCAGAACCCT T C PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:8143726..8143900 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_Splice_Rec_1776066,Human_Splice_Rec_1776170,Human_Splice_Rec_1776172 112468 RMVar_ID_112468 Human_SNP_ID_828499648 m1A Human chr17 - 49704129 49704129 49704129 AACAGGCTCCAACCACATGATGCTGAACATCAACCTTTGGTCGACATTGCTGCTGGGAATGGGTG AACAGGCTCCAACCACATGATGCTGAACATCACCCTTTGGTCGACATTGCTGCTGGGAATGGGTG T G SLC35B1 Ensembl:ENSG00000121073 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:49704124..49705318 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_896686,Human_RBP_ID_1182757,Human_RBP_ID_1861946,Human_RBP_ID_3527507,Human_RBP_ID_5497284,Human_RBP_ID_8456043,Human_RBP_ID_23733479,Human_RBP_ID_26812557 Human_Splice_Rec_1836228,Human_Splice_Rec_1836229,Human_Splice_Rec_1836244,Human_Splice_Rec_1836245,Human_Splice_Rec_1836256,Human_Splice_Rec_1836257,Human_Splice_Rec_1836274,Human_Splice_Rec_1836275,Human_Splice_Rec_1836294,Human_Splice_Rec_1836295,Human_Splice_Rec_1836312,Human_Splice_Rec_1836313,Human_Splice_Rec_1836328,Human_Splice_Rec_1836329,Human_Splice_Rec_1836336,Human_Splice_Rec_1836337,Human_Splice_Rec_1836340,Human_Splice_Rec_1836350,Human_Splice_Rec_1836360,Human_Splice_Rec_1836372,Human_Splice_Rec_1836380 Human_miRNA_ID_2113943,Human_miRNA_ID_2597744 RMVar_hsa_circ_24302,RMVar_hsa_circ_122402,RMVar_hsa_circ_24075,RMVar_hsa_circ_185176,RMVar_hsa_circ_51591,RMVar_hsa_circ_7034,RMVar_hsa_circ_63795 112469 RMVar_ID_112469 Human_SNP_ID_828501036 m1A Human chr17 + 714762 714762 714762 CGACCCCCGCCGCGAGCCCAACTCAGGCCTCCAGCCGCCACCCAGGCCCCAGCACAGCAACTCCC CGACCCCCGCCGCGAGCCCAACTCAGGCCTCCTGCCGCCACCCAGGCCCCAGCACAGCAACTCCC A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:714681..714798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 112470 RMVar_ID_112470 Human_SNP_ID_828502649 m1A Human chr17 - 34980624 34980624 34980624 CCGCCGCGCCGTGCCGCGCCGCGTAGCCCCTCACCTGCCTCTCCGGCTCCGGCGCTCACCGTAGG CCGCCGCGCCGTGCCGCGCCGCGTAGCCCCTCCCCTGCCTCTCCGGCTCCGGCGCTCACCGTAGG T G CCT6B Ensembl:ENSG00000132141 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:34980585..34980678 26863196 MeRIP-seq:(Medium) rs1044406726 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112471 RMVar_ID_112471 Human_SNP_ID_828503181 m1A Human chr17 + 39203079 39203079 39203079 AATGAGGATTTTGCGCCGGCTGCTCAGAAGATACCGTGAATCTAAGAAGATCGATCGCCACATGT AATGAGGATTTTGCGCCGGCTGCTCAGAAGATGCCGTGAATCTAAGAAGATCGATCGCCACATGT A G RPL19 Ensembl:ENSG00000108298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:39203030..39203140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_235768,Human_RBP_ID_764579,Human_RBP_ID_820236,Human_RBP_ID_902106,Human_RBP_ID_1532966,Human_RBP_ID_1856937,Human_RBP_ID_3521896,Human_RBP_ID_4472009,Human_RBP_ID_6590785,Human_RBP_ID_8253386,Human_RBP_ID_8451334,Human_RBP_ID_9375817,Human_RBP_ID_12991723,Human_RBP_ID_18207806,Human_RBP_ID_23724363,Human_RBP_ID_27451605 Human_Splice_Rec_1810856,Human_Splice_Rec_1810857,Human_Splice_Rec_1810866,Human_Splice_Rec_1810867,Human_Splice_Rec_1810875,Human_Splice_Rec_1810884,Human_Splice_Rec_1810885,Human_Splice_Rec_1810894,Human_Splice_Rec_1810895,Human_Splice_Rec_1810902 RMVar_hsa_circ_89600,RMVar_hsa_circ_111948,RMVar_hsa_circ_125189,RMVar_hsa_circ_183862,RMVar_hsa_circ_183863,RMVar_hsa_circ_338344,RMVar_hsa_circ_93090,RMVar_hsa_circ_183864,RMVar_hsa_circ_183865 112472 RMVar_ID_112472 Human_SNP_ID_828506944 m1A Human chr17 - 7496808 7496808 7496808 ACGTGCTTCCATTCCGCATACAGCTCTAGGCCAGAACGCCGGATCCTGGGCTGGTACCGCCCACA ACGTGCTTCCATTCCGCATACAGCTCTAGGCCGGAACGCCGGATCCTGGGCTGGTACCGCCCACA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7496776..7496850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ORCA,mouth squamous_cell_carcinoma 2 head and neck 112473 RMVar_ID_112473 Human_SNP_ID_828524080 m1A Human chr17 + 57368803 57368803 57368803 GTAGATAACAGGTGCTTGTGAGTGAGCTGGAGAGGAGATTGTCAGGGAAGGCTTTCAAGACAAGT GTAGATAACAGGTGCTTGTGAGTGAGCTGGAGGGGAGATTGTCAGGGAAGGCTTTCAAGACAAGT A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:57368800..57368868 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas Human_RBP_ID_6617619 RMVar_hsa_circ_11108,RMVar_hsa_circ_315956,RMVar_hsa_circ_372858,RMVar_hsa_circ_36594,RMVar_hsa_circ_41519,RMVar_hsa_circ_12653,RMVar_hsa_circ_185579,RMVar_hsa_circ_185580,RMVar_hsa_circ_359076,RMVar_hsa_circ_79894,RMVar_hsa_circ_185581 112474 RMVar_ID_112474 Human_SNP_ID_828524219 m1A Human chr17 + 77281529 77281529 77281529 CCGCCACACTTTCCTGGGAGCGGCGGCCACGGAGGCACCATGAAGAAGTCTTACTCAGGTGGGCT CCGCCACACTTTCCTGGGAGCGGCGGCCACGGCGGCACCATGAAGAAGTCTTACTCAGGTGGGCT A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:77281481..77281646 26863196 MeRIP-seq:(Medium) rs8070026 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_9376914,Human_RBP_ID_18419747,Human_RBP_ID_22959682,Human_RBP_ID_26334196 Human_Splice_Rec_1873353,Human_Splice_Rec_1873359,Human_Splice_Rec_1873379 112475 RMVar_ID_112475 Human_SNP_ID_828535723 m1A Human chr17 - 81511376 81511376 81511376 TGAGCGAGGCTACAGCTTCACCACCACGGCCGAGCGGGAAATCGTGCGCGACATCAAGGAGAAGC TGAGCGAGGCTACAGCTTCACCACCACGGCCGGGCGGGAAATCGTGCGCGACATCAAGGAGAAGC T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:81511280..81511462 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_237012,Human_RBP_ID_502520,Human_RBP_ID_766508,Human_RBP_ID_1011048,Human_RBP_ID_1184988,Human_RBP_ID_1544450,Human_RBP_ID_1870698,Human_RBP_ID_3539518,Human_RBP_ID_4458687,Human_RBP_ID_6651175,Human_RBP_ID_8465875,Human_RBP_ID_17262338,Human_RBP_ID_17693313,Human_RBP_ID_17902752,Human_RBP_ID_18191031,Human_RBP_ID_18713778,Human_RBP_ID_20173120,Human_RBP_ID_22807218,Human_RBP_ID_24481549,Human_RBP_ID_26461100,Human_RBP_ID_26814116,Human_RBP_ID_26974459,Human_RBP_ID_27262010,Human_RBP_ID_27458726 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_123222,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187636,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_111725,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_187640,RMVar_hsa_circ_81045,RMVar_hsa_circ_321880,RMVar_hsa_circ_187643,RMVar_hsa_circ_187644 112476 RMVar_ID_112476 Human_SNP_ID_828536621 m1A Human chr17 - 5282732 5282732 5282732 CGCCCTTCCCTCTGCCCTCCCGCAAGCGCTGCACCCGCGCCTCCCGCCCCCTCCCCAGCGACGGC CGCCCTTCCCTCTGCCCTCCCGCAAGCGCTGCCCCCGCGCCTCCCGCCCCCTCCCCAGCGACGGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5282726..5282925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 112477 RMVar_ID_112477 Human_SNP_ID_828543914 m1A Human chr17 + 48937112 48937112 48937112 AGAAGTCCCCCACGCCCAGCATCTCAGACCAAAATCCTTTTCCAGCTACAAGACAGAAAAACAAA AGAAGTCCCCCACGCCCAGCATCTCAGACCAACATCCTTTTCCAGCTACAAGACAGAAAAACAAA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:48937001..48937125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - 112478 RMVar_ID_112478 Human_SNP_ID_828548168 m1A Human chr17 - 39662939 39662939 39662939 CCCTTTCTGGCTCTGGAAGTGGTGGCGACAGGACCCTGGCCCGCAGGGTGGGAGGGGGCACAGTC CCCTTTCTGGCTCTGGAAGTGGTGGCGACAGGGCCCTGGCCCGCAGGGTGGGAGGGGGCACAGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39662888..39663385 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 112479 RMVar_ID_112479 Human_SNP_ID_828549605 m1A Human chr17 + 50150360 50150360 50150360 CAGGAACATACTTTTGATGCGGTGGACGTTGGAGCCATATTTCTTGTGGTGGGCCCCCTTGGGTG CAGGAACATACTTTTGATGCGGTGGACGTTGGCGCCATATTTCTTGTGGTGGGCCCCCTTGGGTG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50150251..50150479 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112480 RMVar_ID_112480 Human_SNP_ID_828550546 m1A Human chr17 - 29942202 29942201 29942202 ATGCAAACAGTGTTAGTAAATGGCATCCAAAAAGAGCTGTGGATTAAACTACTGTCTCATACTTT ATGCAAACAGTGTTAGTAAATGGCATCCAAAA_GAGCTGTGGATTAAACTACTGTCTCATACTTT CT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:29942201..29942303 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - 112481 RMVar_ID_112481 Human_SNP_ID_828551080 m1A Human chr17 - 8148662 8148662 8148662 CACAGCCGTGCTGCCTGCTGATTGCAGAGCGCATCCATTCGGGTTACGAAGGTGGGCAGGTCAGG CACAGCCGTGCTGCCTGCTGATTGCAGAGCGCGTCCATTCGGGTTACGAAGGTGGGCAGGTCAGG T C PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8148056..8148725 32194978 MeRIP-seq:(Medium) rs769554705 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_Splice_Rec_1776045,Human_Splice_Rec_1776087,Human_Splice_Rec_1776129,Human_Splice_Rec_1776187,Human_Splice_Rec_1776225,Human_Splice_Rec_1776251 112482 RMVar_ID_112482 Human_SNP_ID_828551287 m1A Human chr17 + 6643137 6643137 6643137 ATAAATGATGTTAAAAAAACTGGCATGTGTCTAAACAATAGAGTGCTATTAAAATGCCCATGAAC ATAAATGATGTTAAAAAAACTGGCATGTGTCTGAACAATAGAGTGCTATTAAAATGCCCATGAAC A G TXNDC17 Ensembl:ENSG00000129235 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72835775 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_2520881,Human_RBP_ID_3535455 GWAS_ID_13561,GWAS_ID_13562,GWAS_ID_13563,GWAS_ID_13564,GWAS_ID_13565 RMVar_hsa_circ_181730,RMVar_hsa_circ_96198 112483 RMVar_ID_112483 Human_SNP_ID_828557136 m1A Human chr17 + 7229637 7229637 7229637 GCCTCTGCTTCCTTCGCCGCCGGTGGCGCTTAAGGAGGCGGGAGGCACTGCTCTGCTCCGTGGAG GCCTCTGCTTCCTTCGCCGCCGGTGGCGCTTACGGAGGCGGGAGGCACTGCTCTGCTCCGTGGAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7229588..7229674 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus 112484 RMVar_ID_112484 Human_SNP_ID_828557911 m1A Human chr17 - 44207300 44207300 44207300 GGATGACGATGAGGATGAAGATAATGAGTCCGAGGGCAGCAGCTCCAGCTCCTCCTCCTCAGGGG GGATGACGATGAGGATGAAGATAATGAGTCCGGGGGCAGCAGCTCCAGCTCCTCCTCCTCAGGGG T C UBTF Ensembl:ENSG00000108312 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:44207251..44207575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_50375,Human_RBP_ID_201589,Human_RBP_ID_6598721,Human_RBP_ID_8818443,Human_RBP_ID_9376120,Human_RBP_ID_22959220,Human_RBP_ID_23728528,Human_RBP_ID_26330768,Human_RBP_ID_27452979,Human_RBP_ID_27812750 Human_Splice_Rec_1825256,Human_Splice_Rec_1825296,Human_Splice_Rec_1825336,Human_Splice_Rec_1825374,Human_Splice_Rec_1825412,Human_Splice_Rec_1825450,Human_Splice_Rec_1825486,Human_Splice_Rec_1825524 112485 RMVar_ID_112485 Human_SNP_ID_828563072 m1A Human chr17 + 5419613 5419613 5419613 ACACGACGTGGTTAGGAAGCCAGGTCTGCCACAGCTCGCCGTCGCCCACCGGTCCCTCGGCGGCC ACACGACGTGGTTAGGAAGCCAGGTCTGCCACTGCTCGCCGTCGCCCACCGGTCCCTCGGCGGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:5419389..5419675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112486 RMVar_ID_112486 Human_SNP_ID_828563896 m1A Human chr17 - 81512108 81512108 81512108 CGTCATGGTGGGCATGGGCCAGAAGGACTCCTACGTGGGCGACGAGGCCCAGAGCAAGCGTGGCA CGTCATGGTGGGCATGGGCCAGAAGGACTCCTCCGTGGGCGACGAGGCCCAGAGCAAGCGTGGCA T G ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:81511901..81512150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue Human_RBP_ID_49502,Human_RBP_ID_502536,Human_RBP_ID_820951,Human_RBP_ID_897033,Human_RBP_ID_1289491,Human_RBP_ID_1544465,Human_RBP_ID_1870707,Human_RBP_ID_4480554,Human_RBP_ID_5362182,Human_RBP_ID_6651185,Human_RBP_ID_8465888,Human_RBP_ID_8823425,Human_RBP_ID_9326949,Human_RBP_ID_17902757,Human_RBP_ID_18191033,Human_RBP_ID_22223396,Human_RBP_ID_22443242,Human_RBP_ID_22500728,Human_RBP_ID_22587138,Human_RBP_ID_22807222,Human_RBP_ID_26461110,Human_RBP_ID_26974469,Human_RBP_ID_27156937,Human_RBP_ID_27262018,Human_RBP_ID_27458746 Human_Splice_Rec_1880950,Human_Splice_Rec_1880960,Human_Splice_Rec_1880968,Human_Splice_Rec_1880978,Human_Splice_Rec_1880996,Human_Splice_Rec_1881006,Human_Splice_Rec_1881018,Human_Splice_Rec_1881028,Human_Splice_Rec_1881040,Human_Splice_Rec_1881048,Human_Splice_Rec_1881054,Human_Splice_Rec_1881060,Human_Splice_Rec_1881066,Human_Splice_Rec_1881072 Human_miRNA_ID_2435127,Human_miRNA_ID_2435128,Human_miRNA_ID_3027382,Human_miRNA_ID_3027383 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_81045,RMVar_hsa_circ_187644,RMVar_hsa_circ_307034 112487 RMVar_ID_112487 Human_SNP_ID_828563899 m1A Human chr17 - 81512108 81512108 81512108 CGTCATGGTGGGCATGGGCCAGAAGGACTCCTACGTGGGCGACGAGGCCCAGAGCAAGCGTGGCA CGTCATGGTGGGCATGGGCCAGAAGGACTCCTGCGTGGGCGACGAGGCCCAGAGCAAGCGTGGCA T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:81511901..81512150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_49502,Human_RBP_ID_502536,Human_RBP_ID_820951,Human_RBP_ID_897033,Human_RBP_ID_1289491,Human_RBP_ID_1544465,Human_RBP_ID_1870707,Human_RBP_ID_4480554,Human_RBP_ID_5362182,Human_RBP_ID_6651185,Human_RBP_ID_8465888,Human_RBP_ID_8823425,Human_RBP_ID_9326949,Human_RBP_ID_17902757,Human_RBP_ID_18191033,Human_RBP_ID_22223396,Human_RBP_ID_22443242,Human_RBP_ID_22500728,Human_RBP_ID_22587138,Human_RBP_ID_22807222,Human_RBP_ID_26461110,Human_RBP_ID_26974469,Human_RBP_ID_27156937,Human_RBP_ID_27262018,Human_RBP_ID_27458746 Human_Splice_Rec_1880950,Human_Splice_Rec_1880960,Human_Splice_Rec_1880968,Human_Splice_Rec_1880978,Human_Splice_Rec_1880996,Human_Splice_Rec_1881006,Human_Splice_Rec_1881018,Human_Splice_Rec_1881028,Human_Splice_Rec_1881040,Human_Splice_Rec_1881048,Human_Splice_Rec_1881054,Human_Splice_Rec_1881060,Human_Splice_Rec_1881066,Human_Splice_Rec_1881072 Human_miRNA_ID_2435127,Human_miRNA_ID_2435128,Human_miRNA_ID_3027382,Human_miRNA_ID_3027383 RMVar_hsa_circ_78800,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_95896,RMVar_hsa_circ_27847,RMVar_hsa_circ_112049,RMVar_hsa_circ_187637,RMVar_hsa_circ_121801,RMVar_hsa_circ_12910,RMVar_hsa_circ_187641,RMVar_hsa_circ_187642,RMVar_hsa_circ_81045,RMVar_hsa_circ_187644,RMVar_hsa_circ_307034 112488 RMVar_ID_112488 Human_SNP_ID_828565706 m1A Human chr17 + 57106452 57106452 57106452 GAAATGAGGAGGGCTTGGATAGAAATGAGGAGAGCTTGGATAGAAATGAGGAGGGCTTGGATAGA GAAATGAGGAGGGCTTGGATAGAAATGAGGAGGGCTTGGATAGAAATGAGGAGGGCTTGGATAGA A G AKAP1 Ensembl:ENSG00000121057 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs34535433 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia,head_neck squamous_cell_carcinoma 25 head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_6429,Human_RBP_ID_6617075,Human_RBP_ID_13083726,Human_RBP_ID_23118777,Human_RBP_ID_23736534,Human_RBP_ID_26332113 RMVar_hsa_circ_64436,RMVar_hsa_circ_88899,RMVar_hsa_circ_185575 112489 RMVar_ID_112489 Human_SNP_ID_828576126 m1A Human chr17 + 65056640 65056640 65056640 CGCCGCCTCGGCGGGCCCCTCCGGCTCCCTCCACCTCCTCCTCCGGCGGCGGGCGGCTCCGGCAC CGCCGCCTCGGCGGGCCCCTCCGGCTCCCTCCCCCTCCTCCTCCGGCGGCGGGCGGCTCCGGCAC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:65056541..65056781 26863410 MeRIP-seq:(Medium) rs920594875 Functional Loss SNV ICGC 33..33 33 CMDI 1 - 112490 RMVar_ID_112490 Human_SNP_ID_828576565 m1A Human chr17 + 58006416 58006416 58006416 CCATAGCGACCTCGGGGAGCTCCGCCACCTCCACCCCCGCCGCCGCCTCGGCCTGTTCCACGGCC CCATAGCGACCTCGGGGAGCTCCGCCACCTCCCCCCCCGCCGCCGCCTCGGCCTGTTCCACGGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:58006324..58006560;chr17:58006368..58006575 26863196,32194978 MeRIP-seq:(Medium) rs528540802 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112491 RMVar_ID_112491 Human_SNP_ID_828581151 m1A Human chr17 - 30899612 30899612 30899612 ATTATTTCTGTTCCTTTATTTTGTCTTTTTTTAAAAAGATTTCCTCGATCATTTCAAAGATGCCT ATTATTTCTGTTCCTTTATTTTGTCTTTTTTTTAAAAGATTTCCTCGATCATTTCAAAGATGCCT T A TEFM Ensembl:ENSG00000172171 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28539246 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_2501012,Human_RBP_ID_3518401,Human_RBP_ID_6579751,Human_RBP_ID_12958754,Human_RBP_ID_17490220,Human_RBP_ID_25267587 GWAS_ID_15208,GWAS_ID_15209 RMVar_hsa_circ_183298,RMVar_hsa_circ_117801,RMVar_hsa_circ_94342,RMVar_hsa_circ_183297 112492 RMVar_ID_112492 Human_SNP_ID_828581385 m1A Human chr17 - 19341885 19341885 19341885 CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCAACCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA CTCCAAGCTCCTGGCCCAGCCCCTTTTCGCCAGCCATCAGCCCCTCTTTCCTTGCTTTCCTCCCA T C B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19341834..19341968 26863196 MeRIP-seq:(Medium) rs755124474 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 112493 RMVar_ID_112493 Human_SNP_ID_828581815 m1A Human chr17 - 49411743 49411743 49411743 GGAAGGGACTCATTTTCTCATCCCGTGGGTACAGAAACCAATTATCTTTGACTGCCGTTCTCGAC GGAAGGGACTCATTTTCTCATCCCGTGGGTACGGAAACCAATTATCTTTGACTGCCGTTCTCGAC T C PHB Ensembl:ENSG00000167085 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs746659527 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver Human_RBP_ID_492981,Human_RBP_ID_3527393,Human_RBP_ID_4436726,Human_RBP_ID_9073244,Human_RBP_ID_17260560,Human_RBP_ID_17895313,Human_RBP_ID_18701520,Human_RBP_ID_22444745,Human_RBP_ID_26812550,Human_RBP_ID_27454113 Human_Splice_Rec_1835732,Human_Splice_Rec_1835733,Human_Splice_Rec_1835746,Human_Splice_Rec_1835747,Human_Splice_Rec_1835758,Human_Splice_Rec_1835759,Human_Splice_Rec_1835766,Human_Splice_Rec_1835767,Human_Splice_Rec_1835782,Human_Splice_Rec_1835783,Human_Splice_Rec_1835794,Human_Splice_Rec_1835795,Human_Splice_Rec_1835812,Human_Splice_Rec_1835813,Human_Splice_Rec_1835822,Human_Splice_Rec_1835823,Human_Splice_Rec_1835832,Human_Splice_Rec_1835833,Human_Splice_Rec_1835838,Human_Splice_Rec_1835839,Human_Splice_Rec_1835846,Human_Splice_Rec_1835847,Human_Splice_Rec_1835849 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_90200,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185165,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 112494 RMVar_ID_112494 Human_SNP_ID_828585540 m1A Human chr17 - 38726769 38726769 38726769 CTAATTCTGGGAGGGAGGCTTTTGCTAAAAGCAGTGGCATTTCCCCCCACCTTACGCCCTCCCCC CTAATTCTGGGAGGGAGGCTTTTGCTAAAAGCTGTGGCATTTCCCCCCACCTTACGCCCTCCCCC T A lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:38726760..38727011 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112495 RMVar_ID_112495 Human_SNP_ID_828586355 m1A Human chr17 + 2372893 2372893 2372893 CGCCCCAGCCCATTCTCCGTGGGATGGGGCTCACCCAGCTGGGCCACGGTGACTGTGGAGGCTGC CGCCCCAGCCCATTCTCCGTGGGATGGGGCTCGCCCAGCTGGGCCACGGTGACTGTGGAGGCTGC A G SGSM2 Ensembl:ENSG00000141258 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2372889..2373089 32194978 MeRIP-seq:(Medium) rs1486569962 Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_22544127,Human_RBP_ID_22659771 RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_92768,RMVar_hsa_circ_126155,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235,RMVar_hsa_circ_181237,RMVar_hsa_circ_102209,RMVar_hsa_circ_181236,RMVar_hsa_circ_112111,RMVar_hsa_circ_181238,RMVar_hsa_circ_88870,RMVar_hsa_circ_181239,RMVar_hsa_circ_181240 112496 RMVar_ID_112496 Human_SNP_ID_828597867 m1A Human chr17 + 38297196 38297196 38297196 GCGGCCTTTGCGGGAACAAGATGGCAGCCCCCATACCTCAAGGGTTCTCTTGTTTATCGAGGTTT GCGGCCTTTGCGGGAACAAGATGGCAGCCCCCGTACCTCAAGGGTTCTCTTGTTTATCGAGGTTT A G MRPL45 Ensembl:ENSG00000278845 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:38297181..38297308 26863196 MeRIP-seq:(Medium) rs1179413434 Functional Loss SNV TCGA,ICGC 33..33 33 LUSC,UCEC 3 - Human_RBP_ID_1181566,Human_RBP_ID_4465315,Human_RBP_ID_6589708,Human_RBP_ID_18696050 Human_Splice_Rec_1809243,Human_Splice_Rec_1809255 112497 RMVar_ID_112497 Human_SNP_ID_828600407 m1A Human chr17 - 50736929 50736928 50736929 ACCTAGTAAAGAAAAACAAAGGTACTTAAAAAATTGCTTGGTTTTAAAACTTTATTGGAGAAAGG ACCTAGTAAAGAAAAACAAAGGTACTTAAAAA_TTGCTTGGTTTTAAAACTTTATTGGAGAAAGG AT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50736926..50737068 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - 112498 RMVar_ID_112498 Human_SNP_ID_828601799 m1A Human chr17 - 8263579 8263579 8263579 GCTCCAGCTGGGTCACTCAGCTCTTTTAGGACATTGCCTGGTGAGAGGGTTGCAAGGAGAAGCAG GCTCCAGCTGGGTCACTCAGCTCTTTTAGGACGTTGCCTGGTGAGAGGGTTGCAAGGAGAAGCAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8262964..8263826 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 112499 RMVar_ID_112499 Human_SNP_ID_828603796 m1A Human chr17 - 48596361 48596361 48596361 AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGAGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT AGGACGCGAGGGGAAAGGCCTGTGGGGAGCCGCGGGCGTCAGAGAGACCCGGGAAGGAAGGCTCT T G HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12949148 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_17894833,Human_RBP_ID_22715756 112500 RMVar_ID_112500 Human_SNP_ID_828607298 m1A Human chr17 + 38914405 38914405 38914405 GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCACAGGACGGCAGCAGCTACCGGCGGCCCCTGGA GGCGAGGGCATGGAGCCAGAGCGTCGGGATTCGCAGGACGGCAGCAGCTACCGGCGGCCCCTGGA A G LASP1 Ensembl:ENSG00000002834 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs525989 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 11 head and neck Human_RBP_ID_46549,Human_RBP_ID_5185186,Human_RBP_ID_9375805,Human_RBP_ID_22443578,Human_RBP_ID_24545199,Human_RBP_ID_26331680,Human_RBP_ID_26449900,Human_RBP_ID_27812614 Human_Splice_Rec_1810240,Human_Splice_Rec_1810241,Human_Splice_Rec_1810250,Human_Splice_Rec_1810251,Human_Splice_Rec_1810262,Human_Splice_Rec_1810263,Human_Splice_Rec_1810280,Human_Splice_Rec_1810281,Human_Splice_Rec_1810292,Human_Splice_Rec_1810293,Human_Splice_Rec_1810304,Human_Splice_Rec_1810305,Human_Splice_Rec_1810310,Human_Splice_Rec_1810311,Human_Splice_Rec_1810313 GWAS_ID_15210,GWAS_ID_15211,GWAS_ID_15212,GWAS_ID_15213,GWAS_ID_15214 RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852,RMVar_hsa_circ_317229,RMVar_hsa_circ_183853 112501 RMVar_ID_112501 Human_SNP_ID_828608028 m1A Human chr17 - 7576835 7576835 7576835 CTGCACTGGCAGGGAAGCCAGAGGCTCAGATGACACGCATGGGCTCCATCACAGAGCAGCTCTTC CTGCACTGGCAGGGAAGCCAGAGGCTCAGATGCCACGCATGGGCTCCATCACAGAGCAGCTCTTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7576833..7576983 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary 112502 RMVar_ID_112502 Human_SNP_ID_828610776 m1A Human chr17 + 18328779 18328779 18328779 CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGAAGAGAGAGGCGAAGCTCTCAACCTCCTCCCGGA CCTTTAGAAGTCAGGCAGGCCAGGCAGAGGGACGAGAGAGGCGAAGCTCTCAACCTCCTCCCGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18328651..18328900 32194978 MeRIP-seq:(Medium) rs1323562284 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary 112503 RMVar_ID_112503 Human_SNP_ID_828612739 m1A Human chr17 + 50185956 50185956 50185956 AGGTGATGTTCTGGGAGGCCTCGGTGGACATCAGGCGCAGGAAGGTCAGCTGGATGGCCACATCG AGGTGATGTTCTGGGAGGCCTCGGTGGACATCGGGCGCAGGAAGGTCAGCTGGATGGCCACATCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50185909..50186010 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 1 oesophagus 112504 RMVar_ID_112504 Human_SNP_ID_828613131 m1A Human chr17 - 82078821 82078821 82078821 TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCATATTTATTGCATTGCTGGTAGAGACCCCCAGG TCTGCGCTTGGTCTTTCTGTGCTTGGATTTGCTTATTTATTGCATTGCTGGTAGAGACCCCCAGG T A FASN Ensembl:ENSG00000169710 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:82078801..82078825 26863196 MeRIP-seq:(Medium) rs548589236 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_301462,Human_RBP_ID_503429 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 112505 RMVar_ID_112505 Human_SNP_ID_828617819 m1A Human chr17 + 2693916 2693916 2693916 ACAGCCCAGAGGGTACCTCTGCGTAGTCGCCCATGATGTAGTGGAGGCGGGCGAGGAGGCGCAGG ACAGCCCAGAGGGTACCTCTGCGTAGTCGCCCGTGATGTAGTGGAGGCGGGCGAGGAGGCGCAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2692826..2693966 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 112506 RMVar_ID_112506 Human_SNP_ID_828619834 m1A Human chr17 - 7190739 7190739 7190739 GAAGCGTGTCATCGAGGACCTCTCAGGCCCCTACATCTGGGTTCCAGCCCGAGAGAGACTCTGAT GAAGCGTGTCATCGAGGACCTCTCAGGCCCCTGCATCTGGGTTCCAGCCCGAGAGAGACTCTGAT T C DLG4 Ensembl:ENSG00000132535 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7190688..7190789 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_Splice_Rec_1769340,Human_Splice_Rec_1769342,Human_Splice_Rec_1769380,Human_Splice_Rec_1769422,Human_Splice_Rec_1769462,Human_Splice_Rec_1769496,Human_Splice_Rec_1769534,Human_Splice_Rec_1769570,Human_Splice_Rec_1769604,Human_Splice_Rec_1769640,Human_Splice_Rec_1769644,Human_Splice_Rec_1769680,Human_Splice_Rec_1769700 RMVar_hsa_circ_181748 112507 RMVar_ID_112507 Human_SNP_ID_828624620 m1A Human chr17 + 38799378 38799378 38799378 GCTTCTTCTTGGTCTTGGTCTTGCTGGCGCTGAGCGGCGCCACCGCCACCGCCGTGGTGCTGGTG GCTTCTTCTTGGTCTTGGTCTTGCTGGCGCTGGGCGGCGCCACCGCCACCGCCGTGGTGCTGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38799329..38799557 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - 112508 RMVar_ID_112508 Human_SNP_ID_828625634 m1A Human chr17 + 14705465 14705465 14705465 CTTAATGGCAGTGATGGCAAAGGCTATTTTCCACCGCCCATCGATGTTGGTGTTGAGTACTCGCA CTTAATGGCAGTGATGGCAAAGGCTATTTTCCGCCGCCCATCGATGTTGGTGTTGAGTACTCGCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:14705385..14705467 32194978 MeRIP-seq:(Medium) rs878960552 Functional Loss SNV ICGC 33..33 33 STAD 2 - 112509 RMVar_ID_112509 Human_SNP_ID_828627612 m1A Human chr17 + 82082560 82082560 82082560 ACGGCCAGGTTGAAGACGCCGCCCACGGGCCCAAGCTGCGCCGCCTCGGCAATGAGGCCCCGGGC ACGGCCAGGTTGAAGACGCCGCCCACGGGCCCTAGCTGCGCCGCCTCGGCAATGAGGCCCCGGGC A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82082551..82082575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 112510 RMVar_ID_112510 Human_SNP_ID_828635889 m1A Human chr17 - 50750539 50750539 50750539 TGTGTCTTCACTCTGCTTTTCTCGACTACCGGACTTCACACTACTTTTTTTATCATCAGATCCCC TGTGTCTTCACTCTGCTTTTCTCGACTACCGGGCTTCACACTACTTTTTTTATCATCAGATCCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50750501..50750625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 8 brain 112511 RMVar_ID_112511 Human_SNP_ID_828637086 m1A Human chr17 - 17820284 17820284 17820284 TCCCCAGCCTGCACCCACTCCATTGAAGATGTACCCGTCCATGCCCGCTTTCTCCCCTGGGCCTG TCCCCAGCCTGCACCCACTCCATTGAAGATGTGCCCGTCCATGCCCGCTTTCTCCCCTGGGCCTG T C SREBF1 Ensembl:ENSG00000072310 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17820076..17820558 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_5129490,Human_RBP_ID_17079995,Human_RBP_ID_18942914 RMVar_hsa_circ_8278 112512 RMVar_ID_112512 Human_SNP_ID_828639574 m1A Human chr17 + 8207749 8207749 8207749 TCTCCCCCTTGCGCCAGTTACCTGTGGGCTGGACATTGGAGCGGCTCATGAGGACAAGTGCAGAT TCTCCCCCTTGCGCCAGTTACCTGTGGGCTGGTCATTGGAGCGGCTCATGAGGACAAGTGCAGAT A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:8207726..8207750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung 112513 RMVar_ID_112513 Human_SNP_ID_828639604 m1A Human chr17 + 76270200 76270200 76270200 CCCCACACCCGTGTTCTCTCCCGCAGATGTGCACTCCCAGCAACACCCCTGCCACGCCGCCCAAC CCCCACACCCGTGTTCTCTCCCGCAGATGTGCGCTCCCAGCAACACCCCTGCCACGCCGCCCAAC A G UBALD2 Ensembl:ENSG00000185262 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76265208..76270425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_4452591,Human_RBP_ID_5115252,Human_RBP_ID_17264165,Human_RBP_ID_17378544,Human_RBP_ID_18709151,Human_RBP_ID_27260045 Human_Splice_Rec_1871240,Human_Splice_Rec_1871244,Human_Splice_Rec_1871246 RMVar_hsa_circ_101718,RMVar_hsa_circ_187185 112514 RMVar_ID_112514 Human_SNP_ID_828640011 m1A Human chr17 - 17143585 17143583 17143585 GGAGACAGGGGGGAAGCCGAGGCGTCTGGGAGAGGAGCTGGGGGGGCTTCATTGGTGAAGTCCTG GGAGACAGGGGGGAAGCCGAGGCGTCTGGGAG__GAGCTGGGGGGGCTTCATTGGTGAAGTCCTG CCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17142309..17146080 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 UCEC 1 - 112515 RMVar_ID_112515 Human_SNP_ID_828643862 m1A Human chr17 - 4542666 4542666 4542666 CGACAGCACTGAGCTCCTTCCTGACCAAGCGCAACAGCCCCCTCACAGTTCCCATGTTCCTCAGC CGACAGCACTGAGCTCCTTCCTGACCAAGCGCTACAGCCCCCTCACAGTTCCCATGTTCCTCAGC T A MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4542606..4542687 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_3525798,Human_RBP_ID_18700179 Human_Splice_Rec_1763354,Human_Splice_Rec_1763355,Human_Splice_Rec_1763368,Human_Splice_Rec_1763369,Human_Splice_Rec_1763416,Human_Splice_Rec_1763417,Human_Splice_Rec_1763468,Human_Splice_Rec_1763469,Human_Splice_Rec_1763496,Human_Splice_Rec_1763497 RMVar_hsa_circ_792,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 112516 RMVar_ID_112516 Human_SNP_ID_828643863 m1A Human chr17 - 4542666 4542666 4542666 CGACAGCACTGAGCTCCTTCCTGACCAAGCGCAACAGCCCCCTCACAGTTCCCATGTTCCTCAGC CGACAGCACTGAGCTCCTTCCTGACCAAGCGCGACAGCCCCCTCACAGTTCCCATGTTCCTCAGC T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4542606..4542687 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_3525798,Human_RBP_ID_18700179 Human_Splice_Rec_1763354,Human_Splice_Rec_1763355,Human_Splice_Rec_1763368,Human_Splice_Rec_1763369,Human_Splice_Rec_1763416,Human_Splice_Rec_1763417,Human_Splice_Rec_1763468,Human_Splice_Rec_1763469,Human_Splice_Rec_1763496,Human_Splice_Rec_1763497 RMVar_hsa_circ_792,RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 112517 RMVar_ID_112517 Human_SNP_ID_828644608 m1A Human chr17 + 8176259 8176259 8176259 CACCAGATGCGCCAGGAGCGTCAGGAAGCGAGAGGGCACAAGCCCTGAGACCCGGCCCATGGCCC CACCAGATGCGCCAGGAGCGTCAGGAAGCGAGGGGGCACAAGCCCTGAGACCCGGCCCATGGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:8176208..8176338 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid anaplastic_carcinoma 6 head and neck 112518 RMVar_ID_112518 Human_SNP_ID_828645792 m1A Human chr17 + 29390542 29390542 29390542 CGCGAACATCTGAGGCCTCCCGGCCCCGGGGGACCCCGCCCCGCCGTCCGCCGGCCGGCCCGCGG CGCGAACATCTGAGGCCTCCCGGCCCCGGGGGCCCCCGCCCCGCCGTCCGCCGGCCGGCCCGCGG A C AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:29390424..29390675 26863196 MeRIP-seq:(Medium) rs983890741 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_820003,Human_RBP_ID_901735,Human_RBP_ID_3548347,Human_RBP_ID_4464435,Human_RBP_ID_5186488,Human_RBP_ID_18486444 Human_Splice_Rec_1798709 112519 RMVar_ID_112519 Human_SNP_ID_828659873 m1A Human chr17 - 27893188 27893188 27893188 GCCTCGGGTGTCCTCGGATCTATTGAAGACCTAGGGGCGACCCGCGCCGGCACCTTTTCCCTTGC GCCTCGGGTGTCCTCGGATCTATTGAAGACCTGGGGGCGACCCGCGCCGGCACCTTTTCCCTTGC T C LYRM9,AC005697.1 Ensembl:ENSG00000232859,Ensembl:ENSG00000266202 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:27893141..27893311 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary 112520 RMVar_ID_112520 Human_SNP_ID_828663430 m1A Human chr17 + 28813042 28813024 28813042 GCAGAAATTAAGCGGGGGGGGGGGGGGGGGGGAGGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GCAGAAATTAAGCGG__________________GGGGGGGGCGTTGGAGGCATGTTGGGAAAGTA GGGGGGGGGGGGGGGGGGA G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr17:28813001..28813075 26863196 MeRIP-seq:(Medium) rs1489032152 Functional Loss DEL ICGC 16..33 33 COCA 1 - 112521 RMVar_ID_112521 Human_SNP_ID_828674543 m1A Human chr17 - 75131588 75131588 75131588 TTCCCTGAGGAGCCGCACGTGCCGCTGGAGCAACGCCGCGGCTTCCTGGCCCGCGAGCAGTACCG TTCCCTGAGGAGCCGCACGTGCCGCTGGAGCAGCGCCGCGGCTTCCTGGCCCGCGAGCAGTACCG T C NT5C Ensembl:ENSG00000125458 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4788867 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,large_intestine adenocarcinoma 7 head and neck,large intestine Human_RBP_ID_4465657,Human_RBP_ID_9376806,Human_RBP_ID_18992112,Human_RBP_ID_22959490 Human_Splice_Rec_1864571,Human_Splice_Rec_1864579,Human_Splice_Rec_1864591,Human_Splice_Rec_1864613,Human_Splice_Rec_1864621,Human_Splice_Rec_1864631,Human_Splice_Rec_1864637 RMVar_hsa_circ_116495,RMVar_hsa_circ_186962 112522 RMVar_ID_112522 Human_SNP_ID_828679290 m1A Human chr17 + 77498773 77498773 77498773 TATATGATTTTCTCCATTTGTCATCGTTCCCCACCCCTTCGACATGCTGCCAGGAAACAAGGGAA TATATGATTTTCTCCATTTGTCATCGTTCCCCCCCCCTTCGACATGCTGCCAGGAAACAAGGGAA A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:77498724..77498885 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 KICH,kidney chromophobe_renal_cell_carcinoma 16 kidney Human_RBP_ID_50957,Human_RBP_ID_2524267,Human_RBP_ID_6647432,Human_RBP_ID_8191428,Human_RBP_ID_8464369,Human_RBP_ID_17495040,Human_RBP_ID_17654953,Human_RBP_ID_17693173,Human_RBP_ID_18190976,Human_RBP_ID_22061687,Human_RBP_ID_23751460,Human_RBP_ID_24481291,Human_RBP_ID_26458307,Human_RBP_ID_26972458 Human_miRNA_ID_1419193,Human_miRNA_ID_1703340 112523 RMVar_ID_112523 Human_SNP_ID_828683998 m1A Human chr17 - 8222253 8222253 8222253 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGAGTACTAGCAGTTTTGA TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGGTTCCCCGACGGGGAGAGTACTAGCAGTTTTGA T C LINC00324 Ensembl:ENSG00000178977 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1357563321 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_238414,Human_RBP_ID_278785,Human_RBP_ID_504070,Human_RBP_ID_763883,Human_RBP_ID_819952,Human_RBP_ID_901658,Human_RBP_ID_1011327,Human_RBP_ID_1185440,Human_RBP_ID_1370428,Human_RBP_ID_1546359,Human_RBP_ID_1871880,Human_RBP_ID_3540800,Human_RBP_ID_4467434,Human_RBP_ID_5088369,Human_RBP_ID_5097941,Human_RBP_ID_5184945,Human_RBP_ID_5260561,Human_RBP_ID_5649223,Human_RBP_ID_6666721,Human_RBP_ID_8194048,Human_RBP_ID_8255118,Human_RBP_ID_8467509,Human_RBP_ID_9077274,Human_RBP_ID_9326479,Human_RBP_ID_9424660,Human_RBP_ID_9882296,Human_RBP_ID_17081220,Human_RBP_ID_17126576,Human_RBP_ID_17264414,Human_RBP_ID_17582790,Human_RBP_ID_17903749,Human_RBP_ID_18165076,Human_RBP_ID_18544453,Human_RBP_ID_18545444,Human_RBP_ID_18713162,Human_RBP_ID_18943915,Human_RBP_ID_20287179,Human_RBP_ID_22524068,Human_RBP_ID_22544896,Human_RBP_ID_22585286,Human_RBP_ID_22808017,Human_RBP_ID_23130026,Human_RBP_ID_23757476,Human_RBP_ID_24559541,Human_RBP_ID_26749214,Human_RBP_ID_26758211,Human_RBP_ID_27572949,Human_RBP_ID_27670408 112524 RMVar_ID_112524 Human_SNP_ID_828687956 m1A Human chr17 + 27882615 27882615 27882615 GCTTGTAATGCTGCTGGATGCCCTTGGTCGGCAGCTGCTGGCAACAGCGCAGCAAGTATCGGTAG GCTTGTAATGCTGCTGGATGCCCTTGGTCGGCTGCTGCTGGCAACAGCGCAGCAAGTATCGGTAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:27880364..27893317 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas 112525 RMVar_ID_112525 Human_SNP_ID_828691580 m1A Human chr17 + 16382234 16382234 16382234 ATCGAAAATGTGAAGGCCAAGATCCAGGATAAAGAAGGCATCCCTCCCGACCAGCAGAGGCTCAT ATCGAAAATGTGAAGGCCAAGATCCAGGATAAGGAAGGCATCCCTCCCGACCAGCAGAGGCTCAT A G UBB Ensembl:ENSG00000170315 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:16382184..16382454 26863196 MeRIP-seq:(Medium) rs1060199 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm,pharynx nasopharyngeal_carcinoma 11 liver,head and neck Human_RBP_ID_766080,Human_RBP_ID_1528440,Human_RBP_ID_1849805,Human_RBP_ID_3513457,Human_RBP_ID_4468454,Human_RBP_ID_5525373,Human_RBP_ID_6563332,Human_RBP_ID_8253188,Human_RBP_ID_8445082,Human_RBP_ID_9069402,Human_RBP_ID_12902142,Human_RBP_ID_18530464,Human_RBP_ID_18689929,Human_RBP_ID_22209453,Human_RBP_ID_22498776,Human_RBP_ID_22760714,Human_RBP_ID_22803203,Human_RBP_ID_23128903,Human_RBP_ID_24544801,Human_RBP_ID_26811957,Human_RBP_ID_26955121,Human_RBP_ID_27249980,Human_RBP_ID_27448780 Human_miRNA_ID_2870249 RMVar_hsa_circ_83428,RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322,RMVar_hsa_circ_119884,RMVar_hsa_circ_182323,RMVar_hsa_circ_182324 112526 RMVar_ID_112526 Human_SNP_ID_828692804 m1A Human chr17 - 58352137 58352137 58352137 GTCTATCTCCCTGTTGTTCTTCCCATCGGCGAAGATGGCCCTGGAGACGGTGCCGAAGGACCTGC GTCTATCTCCCTGTTGTTCTTCCCATCGGCGAGGATGGCCCTGGAGACGGTGCCGAAGGACCTGC T C SUPT4H1,AC004687.2 Ensembl:ENSG00000213246,Ensembl:ENSG00000285897 Protein coding,Protein coding exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:58352015..58352175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_6904,Human_RBP_ID_495446,Human_RBP_ID_1538370,Human_RBP_ID_4441457,Human_RBP_ID_5237673,Human_RBP_ID_5497448,Human_RBP_ID_9326772,Human_RBP_ID_9376452,Human_RBP_ID_22444797,Human_RBP_ID_22500025,Human_RBP_ID_22959870,Human_RBP_ID_26333652 Human_Splice_Rec_1845519,Human_Splice_Rec_1845525,Human_Splice_Rec_1845533,Human_Splice_Rec_1845552,Human_Splice_Rec_1845553 Human_miRNA_ID_2574693 RMVar_hsa_circ_48327,RMVar_hsa_circ_103878,RMVar_hsa_circ_185639 112527 RMVar_ID_112527 Human_SNP_ID_828700773 m1A Human chr17 + 58007058 58007058 58007058 TGTAGAACACGTCCTCAATGTCCTTGGTTCGGATGTCTGGAGGTAAGTTACCCACGTAGATGCGG TGTAGAACACGTCCTCAATGTCCTTGGTTCGGTTGTCTGGAGGTAAGTTACCCACGTAGATGCGG A T AC015813.5 Ensembl:ENSG00000279069 Other exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:58006673..58007357 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate 112528 RMVar_ID_112528 Human_SNP_ID_828716772 m1A Human chr17 + 3726404 3726404 3726404 GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCATCCCCACAGGAGGGTGGAACTCCCATTCTCAC GTCTTGAAGCCTCTGGTGCTGTTTCAACCTCCGTCCCCACAGGAGGGTGGAACTCCCATTCTCAC A G HASPIN Ensembl:ENSG00000177602 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs170208 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_17259380,Human_RBP_ID_17375284,Human_RBP_ID_17490771 GWAS_ID_13449 112529 RMVar_ID_112529 Human_SNP_ID_828718516 m1A Human chr17 + 75182906 75182906 75182906 GAGGTACCAGGTCCGCACCAAACGAGCACACAAGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG GAGGTACCAGGTCCGCACCAAACGAGCACACAGGCAGCACCAGGAGCGGCAGAAGAAGGAGGCGG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:75182769..75182946 26863410 MeRIP-seq:(Medium) rs1241157161 Functional Loss SNV ICGC 33..33 33 MALY 1 - 112530 RMVar_ID_112530 Human_SNP_ID_828728709 m1A Human chr17 + 62667498 62667498 62667498 CTGCAGCATCGCGCTGCCCTATGTGTGCAAGAAGAAGCCCAACGCCACGGCCGAGCCCACCCCTC CTGCAGCATCGCGCTGCCCTATGTGTGCAAGACGAAGCCCAACGCCACGGCCGAGCCCACCCCTC A C MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:62667375..62667622 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_Splice_Rec_1850811,Human_Splice_Rec_1850869 RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_308737,RMVar_hsa_circ_372334,RMVar_hsa_circ_323827,RMVar_hsa_circ_114480,RMVar_hsa_circ_345839,RMVar_hsa_circ_37407,RMVar_hsa_circ_96956,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186231,RMVar_hsa_circ_75968,RMVar_hsa_circ_186232,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_79263,RMVar_hsa_circ_186234,RMVar_hsa_circ_186235,RMVar_hsa_circ_186236,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237 112531 RMVar_ID_112531 Human_SNP_ID_828729071 m1A Human chr17 + 3680329 3680329 3680329 CAGTGTCCTCCACCCTGCATCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCAGTGTCCT CAGTGTCCTCCACCCTGCATCCTCCACCCTGCGTCCTCCACCCTGCGTCCTCCACCCAGTGTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680326..3680398 26863196 MeRIP-seq:(Medium) rs371332554 Functional Loss SNV ICGC,COSMIC 33..33 33 LUSC,liver hepatocellular_carcinoma 8 liver 112532 RMVar_ID_112532 Human_SNP_ID_828732766 m1A Human chr17 - 75851627 75851627 75851627 ATCACGTGGAACTCACATTCAATGACATGAAGAACGTGCCAGAAGCCTTCAAAGGGACCAAGAAA ATCACGTGGAACTCACATTCAATGACATGAAGTACGTGCCAGAAGCCTTCAAAGGGACCAAGAAA T A WBP2 Ensembl:ENSG00000132471 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75851576..75851715 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_1542327,Human_RBP_ID_1869227,Human_RBP_ID_4451549,Human_RBP_ID_13165534,Human_RBP_ID_17900968,Human_RBP_ID_18708867,Human_RBP_ID_22806740,Human_RBP_ID_26971280 Human_Splice_Rec_1869308,Human_Splice_Rec_1869309,Human_Splice_Rec_1869322,Human_Splice_Rec_1869323,Human_Splice_Rec_1869334,Human_Splice_Rec_1869335,Human_Splice_Rec_1869350,Human_Splice_Rec_1869351,Human_Splice_Rec_1869363,Human_Splice_Rec_1869370,Human_Splice_Rec_1869371,Human_Splice_Rec_1869384,Human_Splice_Rec_1869385,Human_Splice_Rec_1869410,Human_Splice_Rec_1869411,Human_Splice_Rec_1869424,Human_Splice_Rec_1869425,Human_Splice_Rec_1869442,Human_Splice_Rec_1869443,Human_Splice_Rec_1869466,Human_Splice_Rec_1869467,Human_Splice_Rec_1869476,Human_Splice_Rec_1869477,Human_Splice_Rec_1869482,Human_Splice_Rec_1869483,Human_Splice_Rec_1869488,Human_Splice_Rec_1869489,Human_Splice_Rec_1869492 112533 RMVar_ID_112533 Human_SNP_ID_828734263 m1A Human chr17 + 41622353 41622353 41622353 CAGCATCTTTGACCTTCTGCCCCAGCCACCTCACCTCCTCGTGGTTCTTCTTCAGGTAGGCCAGC CAGCATCTTTGACCTTCTGCCCCAGCCACCTCTCCTCCTCGTGGTTCTTCTTCAGGTAGGCCAGC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:41622351..41622565;chr17:41622351..41622556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder 112534 RMVar_ID_112534 Human_SNP_ID_828738692 m1A Human chr17 - 44959787 44959787 44959787 CCCTCCGGGGTGGCGCGCCCGGGGGAGGGGGGAGTTGGGGGCTGGATAGCTTCCCAGCACCCTCA CCCTCCGGGGTGGCGCGCCCGGGGGAGGGGGGGGTTGGGGGCTGGATAGCTTCCCAGCACCCTCA T C C1QL1 Ensembl:ENSG00000131094 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44959742..44960041 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_491242 112535 RMVar_ID_112535 Human_SNP_ID_828739588 m1A Human chr17 - 12167929 12167905 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG_________________________AGGAAGGAC TTCCTTCCTTCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..56 33 SKCA 1 - 112536 RMVar_ID_112536 Human_SNP_ID_828743560 m1A Human chr17 + 81690679 81690679 81690679 GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCAGACTGGGTGGACGCTGAGGAATGCCACCGCTG GTGGTCCTGACTGCTGCCCCTCCTCAGGCCCCGGACTGGGTGGACGCTGAGGAATGCCACCGCTG A G HGS Ensembl:ENSG00000185359 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81690676..81690750 26863196 MeRIP-seq:(Medium) rs757934791 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_237025,Human_RBP_ID_821600,Human_RBP_ID_897051,Human_RBP_ID_2526422,Human_RBP_ID_3953249,Human_RBP_ID_5365300,Human_RBP_ID_9346448,Human_RBP_ID_18470174,Human_RBP_ID_18711649,Human_RBP_ID_18992825,Human_RBP_ID_22543888,Human_RBP_ID_22657008,Human_RBP_ID_22740409,Human_RBP_ID_26332566,Human_RBP_ID_27814377 Human_Splice_Rec_1881550,Human_Splice_Rec_1881551,Human_Splice_Rec_1881564,Human_Splice_Rec_1881565,Human_Splice_Rec_1881604,Human_Splice_Rec_1881605,Human_Splice_Rec_1881626 RMVar_hsa_circ_3701,RMVar_hsa_circ_63128,RMVar_hsa_circ_14992,RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_356496,RMVar_hsa_circ_120983,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_187727,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_82800,RMVar_hsa_circ_94998,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_187734,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_187735 112537 RMVar_ID_112537 Human_SNP_ID_828745708 m1A Human chr17 + 9712019 9712019 9712019 GTCTGATCACTGGCTCTTACGGCTCGGGAGCCACGCTGGCAGCACAAGGGGAAGCCTGCTGTCCT GTCTGATCACTGGCTCTTACGGCTCGGGAGCCTCGCTGGCAGCACAAGGGGAAGCCTGCTGTCCT A T USP43 Ensembl:ENSG00000154914 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:9711926..9712038 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_Splice_Rec_1778472,Human_Splice_Rec_1778500,Human_Splice_Rec_1778528,Human_Splice_Rec_1778552,Human_Splice_Rec_1778568 RMVar_hsa_circ_368545,RMVar_hsa_circ_182098,RMVar_hsa_circ_335161,RMVar_hsa_circ_373139,RMVar_hsa_circ_182102,RMVar_hsa_circ_98030,RMVar_hsa_circ_182104,RMVar_hsa_circ_325495,RMVar_hsa_circ_182105 112538 RMVar_ID_112538 Human_SNP_ID_828745776 m1A Human chr17 - 75042651 75042651 75042651 GTTTTTATTTGACTTATTTTTCAGGATCCCAAAATGGCTGGGCGAAAACTTGCTCTAAAAACCAT GTTTTTATTTGACTTATTTTTCAGGATCCCAAGATGGCTGGGCGAAAACTTGCTCTAAAAACCAT T C ATP5PD Ensembl:ENSG00000167863 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75042601..75042675 26863196 MeRIP-seq:(Medium) rs9660 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA 6 stomach Human_RBP_ID_499294,Human_RBP_ID_904738,Human_RBP_ID_4465651,Human_RBP_ID_9376804,Human_RBP_ID_18708215,Human_RBP_ID_22445745,Human_RBP_ID_26332341,Human_RBP_ID_27259372 Human_Splice_Rec_1864438,Human_Splice_Rec_1864448,Human_Splice_Rec_1864456 GWAS_ID_13183,GWAS_ID_13184 RMVar_hsa_circ_186950,RMVar_hsa_circ_108909,RMVar_hsa_circ_121601,RMVar_hsa_circ_186953,RMVar_hsa_circ_92695,RMVar_hsa_circ_370710,RMVar_hsa_circ_186952,RMVar_hsa_circ_279733,RMVar_hsa_circ_186954,RMVar_hsa_circ_186956 112539 RMVar_ID_112539 Human_SNP_ID_828748308 m1A Human chr17 - 12167929 12167906 12167930 AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGCAGGAAGGCAGGAAGGAAGGAAGGAAGGAAGGAC AGGAAGGCAGGAAGGCAGGAAGGAAGGAAGG________________________AAGGAAGGAC TCCTTCCTTCCTTCCTGCCTTCCTG T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:12167889..12167954 26863196 MeRIP-seq:(Medium) rs796247216 Functional Loss DEL ICGC 32..55 33 ESCA 1 - 112540 RMVar_ID_112540 Human_SNP_ID_828763841 m1A Human chr17 - 29294025 29294025 29294025 GGAGGAGAAGCCCGGCCAGCCACAGCCTCAGCACCATCACAGCCACCACCATCCGCACCATCACC GGAGGAGAAGCCCGGCCAGCCACAGCCTCAGCTCCATCACAGCCACCACCATCCGCACCATCACC T A NUFIP2 Ensembl:ENSG00000108256 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:29293876..29294100 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_RBP_ID_50369,Human_RBP_ID_237597,Human_RBP_ID_768155,Human_RBP_ID_1285335,Human_RBP_ID_4465264,Human_RBP_ID_8448248,Human_RBP_ID_9375633,Human_RBP_ID_17490003,Human_RBP_ID_18419568,Human_RBP_ID_18693113,Human_RBP_ID_22061223,Human_RBP_ID_26331516 112541 RMVar_ID_112541 Human_SNP_ID_828765869 m1A Human chr17 - 4944765 4944765 4944765 ACCCCGATGAACAGGCTGCTTGCAAATGGGGCAGGTCTTCCGGGTCTGAGTGAGCCAGGGGTCCA ACCCCGATGAACAGGCTGCTTGCAAATGGGGCGGGTCTTCCGGGTCTGAGTGAGCCAGGGGTCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4944653..4945107 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 112542 RMVar_ID_112542 Human_SNP_ID_828766714 m1A Human chr17 + 6447547 6447544 6447547 TGAAGGCCAGGAGGCGGAAGAGAGGAGCACAGAAGGGCAGTGGATCCCCAACTCACAGCCTGAGC TGAAGGCCAGGAGGCGGAAGAGAGGAGCAC___AGGGCAGTGGATCCCCAACTCACAGCCTGAGC CAGA C PIMREG Ensembl:ENSG00000129195 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:6447501..6447575 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 COAD 1 - Human_RBP_ID_17899184 Human_Splice_Rec_1767850,Human_Splice_Rec_1767856,Human_Splice_Rec_1767864,Human_Splice_Rec_1767870,Human_Splice_Rec_1767882,Human_Splice_Rec_1767888,Human_Splice_Rec_1767896 RMVar_hsa_circ_34035,RMVar_hsa_circ_93342,RMVar_hsa_circ_181709,RMVar_hsa_circ_181710,RMVar_hsa_circ_289602 112543 RMVar_ID_112543 Human_SNP_ID_828773032 m1A Human chr17 + 44350750 44350750 44350750 CGGACGCACGGTCCCGGTGCCCTGATGGTTCTACCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC CGGACGCACGGTCCCGGTGCCCTGATGGTTCTGCCTGCTGTGAGCTGCCCAGTGGGAAGTATGGC A G GRN Ensembl:ENSG00000030582 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44350676..44350800 32194978 MeRIP-seq:(Medium) rs63750683 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_4431065,Human_RBP_ID_22443731,Human_RBP_ID_22760829,Human_RBP_ID_22804837,Human_RBP_ID_23728636 Human_Splice_Rec_1826090,Human_Splice_Rec_1826091,Human_Splice_Rec_1826104,Human_Splice_Rec_1826105,Human_Splice_Rec_1826148,Human_Splice_Rec_1826149,Human_Splice_Rec_1826160,Human_Splice_Rec_1826161,Human_Splice_Rec_1826172,Human_Splice_Rec_1826173,Human_Splice_Rec_1826176,Human_Splice_Rec_1826177,Human_Splice_Rec_1826187 Human_miRNA_ID_599157,Human_miRNA_ID_1045806,Human_miRNA_ID_2223409,Human_miRNA_ID_2486480,Human_miRNA_ID_3074845 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691 112544 RMVar_ID_112544 Human_SNP_ID_828779563 m1A Human chr17 + 45112261 45112261 45112261 GGGGGAAGGAGGCTGGGATGGCCCACGGGAGGACAGAGGGGAACTGAGGGCCCACAAGTGTCCTG GGGGGAAGGAGGCTGGGATGGCCCACGGGAGGGCAGAGGGGAACTGAGGGCCCACAAGTGTCCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:45112211..45112312;chr17:45112211..45112511 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112545 RMVar_ID_112545 Human_SNP_ID_828779822 m1A Human chr17 - 81252502 81252498 81252502 GGCCAGATGGCGCCGCCTCTGCCCGACTCAGAAAGAGAGAAACAAGAGCCGGAGCAGGGAGAGGT GGCCAGATGGCGCCGCCTCTGCCCGACTCAGA____GAGAAACAAGAGCCGGAGCAGGGAGAGGT CTCTT C SLC38A10 Ensembl:ENSG00000157637 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:81252451..81252625 26863196 MeRIP-seq:(Medium) rs777968247 Functional Loss DEL TCGA 33..36 33 GBM 1 - Human_RBP_ID_502438,Human_RBP_ID_18989518,Human_RBP_ID_23754394 RMVar_hsa_circ_117408,RMVar_hsa_circ_77544,RMVar_hsa_circ_100404,RMVar_hsa_circ_109839,RMVar_hsa_circ_121069,RMVar_hsa_circ_116287,RMVar_hsa_circ_98674,RMVar_hsa_circ_98832,RMVar_hsa_circ_79868,RMVar_hsa_circ_187583,RMVar_hsa_circ_187585,RMVar_hsa_circ_187587,RMVar_hsa_circ_187589,RMVar_hsa_circ_187588,RMVar_hsa_circ_187586,RMVar_hsa_circ_187584,RMVar_hsa_circ_55200,RMVar_hsa_circ_187582,RMVar_hsa_circ_125038,RMVar_hsa_circ_103335,RMVar_hsa_circ_107130,RMVar_hsa_circ_109127,RMVar_hsa_circ_105997,RMVar_hsa_circ_187592,RMVar_hsa_circ_187596,RMVar_hsa_circ_91751,RMVar_hsa_circ_187597,RMVar_hsa_circ_187598,RMVar_hsa_circ_187594,RMVar_hsa_circ_187595,RMVar_hsa_circ_187593,RMVar_hsa_circ_107254,RMVar_hsa_circ_267638,RMVar_hsa_circ_187599 112546 RMVar_ID_112546 Human_SNP_ID_828780346 m1A Human chr17 - 41620749 41620749 41620749 GGCCCAGCTTCGCTGCGAGATGGAGCAGCAGAACCAGGAATACAAAATCCTGCTGGATGTGAAGA GGCCCAGCTTCGCTGCGAGATGGAGCAGCAGAGCCAGGAATACAAAATCCTGCTGGATGTGAAGA T C KRT17 Ensembl:ENSG00000128422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41620599..41620822 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_Splice_Rec_1816257,Human_Splice_Rec_1816271,Human_Splice_Rec_1816283,Human_Splice_Rec_1816289,Human_Splice_Rec_1816293 RMVar_hsa_circ_85034,RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130,RMVar_hsa_circ_76278,RMVar_hsa_circ_105135,RMVar_hsa_circ_118401,RMVar_hsa_circ_119394,RMVar_hsa_circ_83649,RMVar_hsa_circ_88197,RMVar_hsa_circ_184158,RMVar_hsa_circ_184160,RMVar_hsa_circ_184162,RMVar_hsa_circ_184161,RMVar_hsa_circ_184159,RMVar_hsa_circ_120774,RMVar_hsa_circ_184157,RMVar_hsa_circ_88814,RMVar_hsa_circ_114206,RMVar_hsa_circ_184166,RMVar_hsa_circ_184167,RMVar_hsa_circ_184165,RMVar_hsa_circ_184168 112547 RMVar_ID_112547 Human_SNP_ID_828784281 m1A Human chr17 - 29562560 29562560 29562560 TCTTTAACTGGAAGCGATCATACACAAGGTGAAAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA TCTTTAACTGGAAGCGATCATACACAAGGTGAGAGACCTGGCCTGAGAACCCCCAAGTCCTGCAA T C ABHD15 Ensembl:ENSG00000168792 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs539307 Functional Loss SNV ICGC 33..33 33 COCA 5 - 112548 RMVar_ID_112548 Human_SNP_ID_828786719 m1A Human chr17 + 81239028 81239028 81239028 AAGCTCAGGCGGTCCCGTAGCGGCGGCGCGGCAGCCATGATCCAGGTCCCCTCCCGGTCTGCCCC AAGCTCAGGCGGTCCCGTAGCGGCGGCGCGGCGGCCATGATCCAGGTCCCCTCCCGGTCTGCCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:81238764..81239050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 112549 RMVar_ID_112549 Human_SNP_ID_828793085 m1A Human chr17 - 82096445 82096445 82096445 GGCACTCACACCGCCCGCCCTGCAGAGCAGCCATGGAGGAGGTGGTGATTGCCGGCATGTCCGGG GGCACTCACACCGCCCGCCCTGCAGAGCAGCCGTGGAGGAGGTGGTGATTGCCGGCATGTCCGGG T C FASN Ensembl:ENSG00000169710 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82096376..82096556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_901229,Human_RBP_ID_4481399,Human_RBP_ID_5368726,Human_RBP_ID_8093106,Human_RBP_ID_19080725,Human_RBP_ID_22544026,Human_RBP_ID_22587273,Human_RBP_ID_22657147,Human_RBP_ID_22740448,Human_RBP_ID_26781335 Human_Splice_Rec_1884364,Human_Splice_Rec_1884448,Human_Splice_Rec_1884552,Human_Splice_Rec_1884560,Human_Splice_Rec_1884562 Human_miRNA_ID_2017013,Human_miRNA_ID_2172423 RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_110978,RMVar_hsa_circ_7784,RMVar_hsa_circ_187889,RMVar_hsa_circ_39951 112550 RMVar_ID_112550 Human_SNP_ID_828793905 m1A Human chr17 - 40818884 40818884 40818884 GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCAGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC GCGGCTACGGGGGCGGCAGCTCCGGCGGCGGCGGCAGCTCCGGCGGCGGATACGGCGGCGGCAGC T C KRT10 Ensembl:ENSG00000186395 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:40818776..40818999 26863410 MeRIP-seq:(Medium) rs1426480004 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 1 stomach Human_RBP_ID_237077,Human_RBP_ID_764122,Human_RBP_ID_820448,Human_RBP_ID_902006,Human_RBP_ID_4425768,Human_RBP_ID_5496986,Human_RBP_ID_8941820,Human_RBP_ID_18419596 Human_Splice_Rec_1815551 RMVar_hsa_circ_77220,RMVar_hsa_circ_98115,RMVar_hsa_circ_88448,RMVar_hsa_circ_89067,RMVar_hsa_circ_84882,RMVar_hsa_circ_184098,RMVar_hsa_circ_184100,RMVar_hsa_circ_184101,RMVar_hsa_circ_184102,RMVar_hsa_circ_184099 112551 RMVar_ID_112551 Human_SNP_ID_828798170 m1A Human chr17 + 49411813 49411813 49411813 CACAATGTCCTGCACTCCACGGAATCGGTCAAAGATGACAGCTCTGTGCCCAGCATCCACTAGGA CACAATGTCCTGCACTCCACGGAATCGGTCAACGATGACAGCTCTGTGCCCAGCATCCACTAGGA A C AC091180.6 Ensembl:ENSG00000262039 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:49411641..49411873;chr17:49411676..49411902 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 112552 RMVar_ID_112552 Human_SNP_ID_828799119 m1A Human chr17 - 38297226 38297226 38297226 CCTACCCACCTGCCGAGACCACCAGCCCAAAAACCTCGATAAACAAGAGAACCCTTGAGGTATGG CCTACCCACCTGCCGAGACCACCAGCCCAAAACCCTCGATAAACAAGAGAACCCTTGAGGTATGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38297217..38298514 32194978 MeRIP-seq:(Medium) rs9890011 Functional Loss SNV ICGC 33..33 33 THCA 1 - 112553 RMVar_ID_112553 Human_SNP_ID_828803250 m1A Human chr17 + 10695700 10695699 10695701 AACAACAAAAAAGGTGCTAGTCCATAGCCAGGAAGACCTTTATACAGGGCTGAGCAGATGATAAT AACAACAAAAAAGGTGCTAGTCCATAGCCAGG__GACCTTTATACAGGGCTGAGCAGATGATAAT GAA G lnc-ADPRM-6 RNACentral:URS0000D5D6C5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:10695696..10695771 26863196 MeRIP-seq:(Medium) rs199665575 Functional Loss DEL ICGC 33..34 33 COCA 1 - 112554 RMVar_ID_112554 Human_SNP_ID_828803973 m1A Human chr17 + 45148602 45148597 45148602 GGAAAAGAGGAGGAGGCGGAGGAGAACTGAGCAGAGCAGAGCATCGAGCCAAAGGGGAGATGAGT GGAAAAGAGGAGGAGGCGGAGGAGAACT_____GAGCAGAGCATCGAGCCAAAGGGGAGATGAGT TGAGCA T HEXIM1 Ensembl:ENSG00000186834 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:45148476..45149433 26863196 MeRIP-seq:(Medium) rs982605629 Functional Loss DEL ICGC 29..33 33 CHOL 1 - Human_RBP_ID_897672,Human_RBP_ID_1546657,Human_RBP_ID_3541722,Human_RBP_ID_3950754,Human_RBP_ID_4464617,Human_RBP_ID_5088254,Human_RBP_ID_5143256,Human_RBP_ID_6600910,Human_RBP_ID_8192041,Human_RBP_ID_8232026,Human_RBP_ID_8941826,Human_RBP_ID_9422360,Human_RBP_ID_17653859,Human_RBP_ID_17669960,Human_RBP_ID_18419629,Human_RBP_ID_18544410,Human_RBP_ID_18941780,Human_RBP_ID_22061419,Human_RBP_ID_22357302,Human_RBP_ID_22523793,Human_RBP_ID_22717441,Human_RBP_ID_23118764,Human_RBP_ID_24545021,Human_RBP_ID_24552303,Human_RBP_ID_26331957,Human_RBP_ID_26769319,Human_RBP_ID_27812787 112555 RMVar_ID_112555 Human_SNP_ID_828804408 m1A Human chr17 - 81888351 81888351 81888351 CTGGAGGTTTTGGTGGTGGTGGAGGCACCCGGAGAGGCACCCGCGGAGGCGCCCGTGGAAGAGGC CTGGAGGTTTTGGTGGTGGTGGAGGCACCCGGGGAGGCACCCGCGGAGGCGCCCGTGGAAGAGGC T C ALYREF Ensembl:ENSG00000183684 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:81888226..81888407 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_237005,Human_RBP_ID_302012,Human_RBP_ID_503019,Human_RBP_ID_764117,Human_RBP_ID_821718,Human_RBP_ID_4460083,Human_RBP_ID_5365354,Human_RBP_ID_6652572,Human_RBP_ID_8823600,Human_RBP_ID_22061810,Human_RBP_ID_26332585,Human_RBP_ID_27262490 Human_Splice_Rec_1882312,Human_Splice_Rec_1882318 RMVar_hsa_circ_187783,RMVar_hsa_circ_117321,RMVar_hsa_circ_56804 112556 RMVar_ID_112556 Human_SNP_ID_828805769 m1A Human chr17 + 50707811 50707811 50707811 CTGCTCGCGCCGCTGCCCGCGCCCGCCCCGGGACTTCCGCTCCCTCCCGCGGGCCGCCCCTGCTG CTGCTCGCGCCGCTGCCCGCGCCCGCCCCGGGGCTTCCGCTCCCTCCCGCGGGCCGCCCCTGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:50707465..50707925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112557 RMVar_ID_112557 Human_SNP_ID_828807353 m1A Human chr17 - 30522359 30522359 30522359 TGAAGATGTCCCATCAATGGAACGCATACAGCAGCAACAGGATGGTACAGATCCCAATAACACCC TGAAGATGTCCCATCAATGGAACGCATACAGCGGCAACAGGATGGTACAGATCCCAATAACACCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:30522327..30522433 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 112558 RMVar_ID_112558 Human_SNP_ID_828808670 m1A Human chr17 + 79082031 79082031 79082031 TGTACGTGGGCGTGGATGTGTTTGCTCGAGGGAACGTGGTCGGAGGCCGATTCGACACAGACAAG TGTACGTGGGCGTGGATGTGTTTGCTCGAGGGGACGTGGTCGGAGGCCGATTCGACACAGACAAG A G ENGASE Ensembl:ENSG00000167280 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79081915..79082119 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas pancreatoblastoma 1 pancreas Human_RBP_ID_48826,Human_RBP_ID_896973,Human_RBP_ID_3951218,Human_RBP_ID_22740993,Human_RBP_ID_22957885,Human_RBP_ID_23752563,Human_RBP_ID_26332480 Human_Splice_Rec_1876711,Human_Splice_Rec_1876745 RMVar_hsa_circ_346304,RMVar_hsa_circ_373275,RMVar_hsa_circ_344659,RMVar_hsa_circ_54050,RMVar_hsa_circ_187430,RMVar_hsa_circ_90891,RMVar_hsa_circ_187433,RMVar_hsa_circ_122186,RMVar_hsa_circ_187434 112559 RMVar_ID_112559 Human_SNP_ID_828810232 m1A Human chr17 + 77402455 77402455 77402455 TCGGAGGACGGAGATCACCATCGTCAAACCCCAGGAGTCAGCCCACCGGAGGATGGAGCCCCCTG TCGGAGGACGGAGATCACCATCGTCAAACCCCGGGAGTCAGCCCACCGGAGGATGGAGCCCCCTG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:77402368..77402625 26863196 MeRIP-seq:(Medium) rs376473706 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 10 oesophagus Human_RBP_ID_26332446,Human_RBP_ID_26814033 Human_Splice_Rec_1873499 Human_miRNA_ID_2041254,Human_miRNA_ID_2454551,Human_miRNA_ID_2874061,Human_miRNA_ID_2982023,Human_miRNA_ID_3020237 RMVar_hsa_circ_52125,RMVar_hsa_circ_274220,RMVar_hsa_circ_360688,RMVar_hsa_circ_187289 112560 RMVar_ID_112560 Human_SNP_ID_828811457 m1A Human chr17 + 45114748 45114748 45114748 AGCGCTCTCCCCTCTTCACCTGGCTGCTTCCTAGTCCTCCAGGTGATGTGTCCTCTCAGCATCAC AGCGCTCTCCCCTCTTCACCTGGCTGCTTCCTTGTCCTCCAGGTGATGTGTCCTCTCAGCATCAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:45114743..45115080 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 112561 RMVar_ID_112561 Human_SNP_ID_828812970 m1A Human chr17 + 979368 979368 979368 TGTAGGGCAGCGCCAGCCACGGCATGTCCCGCACGAAGTCCTGCCACTGCCGCTGGTCCTGGTCC TGTAGGGCAGCGCCAGCCACGGCATGTCCCGCGCGAAGTCCTGCCACTGCCGCTGGTCCTGGTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:979301..979775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 112562 RMVar_ID_112562 Human_SNP_ID_828817226 m1A Human chr17 + 75504916 75504916 75504916 GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCAGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA GAGGCTGCGGTGTCCGGGAGAAGCCTGGGCGCGGGGGGGTGGGTGCGGAGGGGAGGCGGGCTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75504871..75504968 26863196 MeRIP-seq:(Medium) rs760588063 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 112563 RMVar_ID_112563 Human_SNP_ID_828819945 m1A Human chr17 - 75904630 75904630 75904630 TGAGCAACCTGGAGCGGCTGGAGAAGTACCGGAGCTTCGACCGCTACCGGCGCCGAGCAGAGCAG TGAGCAACCTGGAGCGGCTGGAGAAGTACCGGGGCTTCGACCGCTACCGGCGCCGAGCAGAGCAG T C MRPL38,AC087289.3 Ensembl:ENSG00000204316,Ensembl:ENSG00000267426 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75904581..75905674 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_500172,Human_RBP_ID_822262,Human_RBP_ID_896876,Human_RBP_ID_4467365,Human_RBP_ID_5441922,Human_RBP_ID_9376847,Human_RBP_ID_18989254,Human_RBP_ID_19086646,Human_RBP_ID_22061650,Human_RBP_ID_22221284,Human_RBP_ID_22959663,Human_RBP_ID_26330878,Human_RBP_ID_26971381 Human_Splice_Rec_1869576,Human_Splice_Rec_1869577,Human_Splice_Rec_1869622,Human_Splice_Rec_1869623,Human_Splice_Rec_1869632,Human_Splice_Rec_1869633,Human_Splice_Rec_1869642,Human_Splice_Rec_1869643,Human_Splice_Rec_1869650,Human_Splice_Rec_1869651,Human_Splice_Rec_1869658,Human_Splice_Rec_1869664,Human_Splice_Rec_1869670,Human_Splice_Rec_1869671,Human_Splice_Rec_1869678,Human_Splice_Rec_1869679,Human_Splice_Rec_1869740,Human_Splice_Rec_1869741,Human_Splice_Rec_1869760 RMVar_hsa_circ_97784,RMVar_hsa_circ_114087,RMVar_hsa_circ_187116,RMVar_hsa_circ_79852,RMVar_hsa_circ_93982,RMVar_hsa_circ_187117,RMVar_hsa_circ_187118,RMVar_hsa_circ_187115,RMVar_hsa_circ_62723,RMVar_hsa_circ_104568,RMVar_hsa_circ_187120 112564 RMVar_ID_112564 Human_SNP_ID_828821007 m1A Human chr17 - 6579726 6579726 6579726 GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCATTTGTGTCACACTGGAGAAGGGATGGCACCAC GCTGCTACATAAAGGCTCTCTGAGGCGAGGCCGTTTGTGTCACACTGGAGAAGGGATGGCACCAC T C KIAA0753 Ensembl:ENSG00000198920 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3744720 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue GWAS_ID_13461,GWAS_ID_13462,GWAS_ID_13463,GWAS_ID_13464,GWAS_ID_13465,GWAS_ID_13466,GWAS_ID_13467,GWAS_ID_13468,GWAS_ID_13469,GWAS_ID_13470,GWAS_ID_13471,GWAS_ID_13472,GWAS_ID_13473,GWAS_ID_13474,GWAS_ID_13475,GWAS_ID_13476,GWAS_ID_13477,GWAS_ID_13478,GWAS_ID_13479,GWAS_ID_13480,GWAS_ID_13481,GWAS_ID_13482,GWAS_ID_13483,GWAS_ID_13484,GWAS_ID_13485,GWAS_ID_13486,GWAS_ID_13487,GWAS_ID_13488,GWAS_ID_13489,GWAS_ID_13490,GWAS_ID_13491,GWAS_ID_13492,GWAS_ID_13493,GWAS_ID_13494,GWAS_ID_13495,GWAS_ID_13496,GWAS_ID_13497,GWAS_ID_13498,GWAS_ID_13499,GWAS_ID_13500,GWAS_ID_13501,GWAS_ID_13502,GWAS_ID_13503,GWAS_ID_13504,GWAS_ID_13505,GWAS_ID_13506,GWAS_ID_13507,GWAS_ID_13508,GWAS_ID_13509 RMVar_hsa_circ_181719 112565 RMVar_ID_112565 Human_SNP_ID_828833895 m1A Human chr17 - 17227956 17227956 17227956 TGGCATTCAGATGAACAGTCGGATGCGTGCGCACAGCCCCGCAGAGGGGGCCAGCGTCGAGTCCA TGGCATTCAGATGAACAGTCGGATGCGTGCGCGCAGCCCCGCAGAGGGGGCCAGCGTCGAGTCCA T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17227915..17228000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_12906746,Human_RBP_ID_17886178,Human_RBP_ID_26332969 Human_Splice_Rec_1785326 Human_miRNA_ID_3066223 RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_7049,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_334202,RMVar_hsa_circ_31054,RMVar_hsa_circ_299845,RMVar_hsa_circ_182388 112566 RMVar_ID_112566 Human_SNP_ID_828836824 m1A Human chr17 - 76736832 76736832 76736832 CCACAGCCGCCGGGGACCGCCACCCCGCAGGTACGGGGGCGGTGGCTACGGACGCCGGAGCCGCA CCACAGCCGCCGGGGACCGCCACCCCGCAGGTGCGGGGGCGGTGGCTACGGACGCCGGAGCCGCA T C SRSF2 Ensembl:ENSG00000161547 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr17:76736826..76736850;chr17:76736801..76736992 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 middle_lobe adenocarcinoma,lung adenocarcinoma,LUAD 9 lung Human_RBP_ID_1010722,Human_RBP_ID_4479334,Human_RBP_ID_5497865,Human_RBP_ID_6646666,Human_RBP_ID_18439732,Human_RBP_ID_22443912,Human_RBP_ID_27838538 Human_Splice_Rec_1872425,Human_Splice_Rec_1872429,Human_Splice_Rec_1872431,Human_Splice_Rec_1872443,Human_Splice_Rec_1872463 RMVar_hsa_circ_187247,RMVar_hsa_circ_90518 112567 RMVar_ID_112567 Human_SNP_ID_828836939 m1A Human chr17 - 28328722 28328722 28328722 TCTAACAATTTTGTTTTTCAGGTATCGGGTTGAATATGAAGCTTTGTGTAAAGTAGAAGCAGAAC TCTAACAATTTTGTTTTTCAGGTATCGGGTTGTATATGAAGCTTTGTGTAAAGTAGAAGCAGAAC T A IFT20 Ensembl:ENSG00000109083 Protein coding stop codon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:28328374..28328722 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 8 lung Human_RBP_ID_485629,Human_RBP_ID_1851815,Human_RBP_ID_6572671,Human_RBP_ID_9849916,Human_RBP_ID_12938081,Human_RBP_ID_22498988,Human_RBP_ID_24559064,Human_RBP_ID_25259654 Human_Splice_Rec_1794936,Human_Splice_Rec_1794950,Human_Splice_Rec_1794960,Human_Splice_Rec_1794968,Human_Splice_Rec_1794978,Human_Splice_Rec_1794988 RMVar_hsa_circ_124541,RMVar_hsa_circ_182824 112568 RMVar_ID_112568 Human_SNP_ID_828837674 m1A Human chr17 + 44351142 44351142 44351142 TCTCCAAGGAGAACGCTACCACGGACCTCCTCACTAAGCTGCCTGCGCACACAGGTACCAGAGGC TCTCCAAGGAGAACGCTACCACGGACCTCCTCGCTAAGCTGCCTGCGCACACAGGTACCAGAGGC A G GRN Ensembl:ENSG00000030582 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44351009..44351161 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1286665,Human_RBP_ID_1368499,Human_RBP_ID_22760831,Human_RBP_ID_26812444 Human_Splice_Rec_1826107,Human_Splice_Rec_1826163,Human_Splice_Rec_1826179 RMVar_hsa_circ_35457,RMVar_hsa_circ_99218,RMVar_hsa_circ_96477,RMVar_hsa_circ_184685,RMVar_hsa_circ_33714,RMVar_hsa_circ_81887,RMVar_hsa_circ_184686,RMVar_hsa_circ_102283,RMVar_hsa_circ_184687,RMVar_hsa_circ_87715,RMVar_hsa_circ_184688,RMVar_hsa_circ_85004,RMVar_hsa_circ_184689,RMVar_hsa_circ_106530,RMVar_hsa_circ_116702,RMVar_hsa_circ_184690,RMVar_hsa_circ_184691,RMVar_hsa_circ_265063,RMVar_hsa_circ_184692,RMVar_hsa_circ_46629,RMVar_hsa_circ_268864 112569 RMVar_ID_112569 Human_SNP_ID_828842029 m1A Human chr17 - 50140130 50140130 50140130 GGAACAGGAGCGATGGCAGCGGGAGATGATGGAGCAGAGATACGCCCAGTATGGGGAGGATGACG GGAACAGGAGCGATGGCAGCGGGAGATGATGGGGCAGAGATACGCCCAGTATGGGGAGGATGACG T C PPP1R9B Ensembl:ENSG00000108819 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50135585..50140157 32194978 MeRIP-seq:(Medium) rs781550890 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_3952664,Human_RBP_ID_9290207,Human_RBP_ID_9376329,Human_RBP_ID_13064480,Human_RBP_ID_23733881,Human_RBP_ID_26332041 Human_Splice_Rec_1837328,Human_Splice_Rec_1837329,Human_Splice_Rec_1837345 Human_miRNA_ID_2924403 RMVar_hsa_circ_185248,RMVar_hsa_circ_122262,RMVar_hsa_circ_332463,RMVar_hsa_circ_185247 112570 RMVar_ID_112570 Human_SNP_ID_828842624 m1A Human chr17 + 42114943 42114943 42114943 ATGTGGGACAGCTCCGTGTAGGGGATGCGGGGATTCAGCTCACACTCCATCAGCGTCGCTCCCTC ATGTGGGACAGCTCCGTGTAGGGGATGCGGGGTTTCAGCTCACACTCCATCAGCGTCGCTCCCTC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42114869..42115001 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 112571 RMVar_ID_112571 Human_SNP_ID_828842918 m1A Human chr17 + 16382199 16382199 16382199 AGACCATCACCCTGGAAGTGGAGCCCAGTGACACCATCGAAAATGTGAAGGCCAAGATCCAGGAT AGACCATCACCCTGGAAGTGGAGCCCAGTGACGCCATCGAAAATGTGAAGGCCAAGATCCAGGAT A G UBB Ensembl:ENSG00000170315 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:16382176..16382200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_483797,Human_RBP_ID_8253188,Human_RBP_ID_9069402,Human_RBP_ID_18530463,Human_RBP_ID_22803203,Human_RBP_ID_26955121,Human_RBP_ID_27249979,Human_RBP_ID_27448780 Human_miRNA_ID_2022684,Human_miRNA_ID_2261224,Human_miRNA_ID_2264272,Human_miRNA_ID_2267338 RMVar_hsa_circ_83428,RMVar_hsa_circ_84603,RMVar_hsa_circ_126997,RMVar_hsa_circ_182321,RMVar_hsa_circ_182322,RMVar_hsa_circ_119884,RMVar_hsa_circ_182323,RMVar_hsa_circ_182324 112572 RMVar_ID_112572 Human_SNP_ID_828844537 m1A Human chr17 - 43661759 43661759 43661759 TGGTGCATTGGAGGGGCAGGAGCAAGCCCGACATAGGTGTGTGCACACACATAGGAGTAGCTGGC TGGTGCATTGGAGGGGCAGGAGCAAGCCCGACCTAGGTGTGTGCACACACATAGGAGTAGCTGGC T G MEOX1 Ensembl:ENSG00000005102 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43661708..43661899 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112573 RMVar_ID_112573 Human_SNP_ID_828857272 m1A Human chr17 + 58631745 58631741 58631745 AACACTGCTATCCCACTCGTGAGAGAACACAAATATCTCCCTCTCGCGGTTTCCAGCGTTCTACA AACACTGCTATCCCACTCGTGAGAGAACA____TATCTCCCTCTCGCGGTTTCCAGCGTTCTACA ACAAA A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:58631695..58631760 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 LMS 1 - 112574 RMVar_ID_112574 Human_SNP_ID_828858198 m1A Human chr17 + 44960208 44960208 44960208 GACGTGGGGAGCTCAGTCGGAGTAGATGATGAAGCCAGAGAACGTGCTGTATTTGTTGCTGTTGC GACGTGGGGAGCTCAGTCGGAGTAGATGATGACGCCAGAGAACGTGCTGTATTTGTTGCTGTTGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:44959837..44960325;chr17:44959844..44960300;chr17:44959892..44960275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 112575 RMVar_ID_112575 Human_SNP_ID_828864261 m1A Human chr17 + 82088028 82088028 82088028 GGGAGGCCTCCAGGAGCCGTACCTCCAGGGACACTGTCCCTGCAGAGCGGGAGAGTTGGAGATCA GGGAGGCCTCCAGGAGCCGTACCTCCAGGGACGCTGTCCCTGCAGAGCGGGAGAGTTGGAGATCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82087978..82088210 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LGG 1 - 112576 RMVar_ID_112576 Human_SNP_ID_828866054 m1A Human chr17 - 75631459 75631459 75631459 GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGACTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC GCTGTATGAGGGAGGCCGCAAGGGCTACGGGGGCTTCAGCAGGTAAGGGGCCGAGAAGCCAGGGC T C RECQL5 Ensembl:ENSG00000108469 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs820196 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,COCA,salivary_gland mucinous_adenocarcinoma 9 head and neck,breast Human_RBP_ID_900739,Human_RBP_ID_18708661,Human_RBP_ID_27814280 Human_Splice_Rec_1867855,Human_Splice_Rec_1867891,Human_Splice_Rec_1867927,Human_Splice_Rec_1867961 GWAS_ID_13185,GWAS_ID_13186,GWAS_ID_13187,GWAS_ID_13188,GWAS_ID_13189,GWAS_ID_13190,GWAS_ID_13191,GWAS_ID_13192 RMVar_hsa_circ_117920,RMVar_hsa_circ_62148,RMVar_hsa_circ_187057,RMVar_hsa_circ_82823,RMVar_hsa_circ_187056 112577 RMVar_ID_112577 Human_SNP_ID_828869227 m1A Human chr17 - 50737025 50737025 50737025 TTGATAAAAGTTACACAGAAAATTCACTTACCAAGATCAGAACGTGTATTTGTGAACAATTCCGC TTGATAAAAGTTACACAGAAAATTCACTTACCGAGATCAGAACGTGTATTTGTGAACAATTCCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr17:50736926..50737322;chr17:50737012..50737471 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 4 skin,head and neck 112578 RMVar_ID_112578 Human_SNP_ID_828870424 m1A Human chr17 - 80050118 80050118 80050118 CTGCAGGTGTACCAGGTGCTGCTGCACCTCATAGAGATTCACCCCCAGCTCCTGCCGCTGGGCTC CTGCAGGTGTACCAGGTGCTGCTGCACCTCATGGAGATTCACCCCCAGCTCCTGCCGCTGGGCTC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:80050084..80050210 26863196 MeRIP-seq:(Medium) rs371604414 Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 4 lung 112579 RMVar_ID_112579 Human_SNP_ID_828873597 m1A Human chr17 - 50356184 50356184 50356184 GCCACACCAGTCCACAATGTGCTTGTACTGGCACTTGCAGCCCAGCTTGCGGTTCCAGTTGGTGA GCCACACCAGTCCACAATGTGCTTGTACTGGCTCTTGCAGCCCAGCTTGCGGTTCCAGTTGGTGA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:50356076..50356250 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_1536770 112580 RMVar_ID_112580 Human_SNP_ID_828882550 m1A Human chr17 - 38764103 38764103 38764103 TGATTTTGTCCTTCTCGCTGCAGAGGGAGAAAATCACAAGAAAACATCTCTACCCATCTGGACCG TGATTTTGTCCTTCTCGCTGCAGAGGGAGAAATTCACAAGAAAACATCTCTACCCATCTGGACCG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:38764101..38764225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112581 RMVar_ID_112581 Human_SNP_ID_828883164 m1A Human chr17 + 46923209 46923209 46923209 CTGCGGGGCCGGCGACATGGATCCCCTGTTCCAGCAAACGCACAAGTGAGGGCCGGTCGGGGAGC CTGCGGGGCCGGCGACATGGATCCCCTGTTCCTGCAAACGCACAAGTGAGGGCCGGTCGGGGAGC A T AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:46923159..46923285 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 25 oesophagus Human_RBP_ID_1535572,Human_RBP_ID_4433376,Human_RBP_ID_9378397,Human_RBP_ID_18419634,Human_RBP_ID_18700277 Human_Splice_Rec_1830763,Human_Splice_Rec_1830771,Human_Splice_Rec_1830785,Human_Splice_Rec_1830793,Human_Splice_Rec_1830807,Human_Splice_Rec_1830817,Human_Splice_Rec_1830829,Human_Splice_Rec_1830831,Human_Splice_Rec_1830839,Human_Splice_Rec_1830849,Human_Splice_Rec_1830861,Human_Splice_Rec_1830873,Human_Splice_Rec_1830885,Human_Splice_Rec_1830889,Human_Splice_Rec_1830897,Human_Splice_Rec_1830905,Human_Splice_Rec_1830919,Human_Splice_Rec_1830929,Human_Splice_Rec_1830939,Human_Splice_Rec_1830945,Human_Splice_Rec_1830969,Human_Splice_Rec_1830985,Human_Splice_Rec_1830995,Human_Splice_Rec_1831005,Human_Splice_Rec_1831017,Human_Splice_Rec_1831033,Human_Splice_Rec_1831039,Human_Splice_Rec_1831047,Human_Splice_Rec_1831065,Human_Splice_Rec_1831083,Human_Splice_Rec_1831103,Human_Splice_Rec_1831111,Human_Splice_Rec_1831129,Human_Splice_Rec_1831139,Human_Splice_Rec_1831147,Human_Splice_Rec_1831197,Human_Splice_Rec_1831215 112582 RMVar_ID_112582 Human_SNP_ID_828884339 m1A Human chr17 - 5378631 5378631 5378631 TAAATCAAGGAACAGTGAGGTCAGGAAGTTGAATGGGGTTACTATGAAAGGAACTAATGATGTCT TAAATCAAGGAACAGTGAGGTCAGGAAGTTGATTGGGGTTACTATGAAAGGAACTAATGATGTCT T A NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:5378627..5378931 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_13077405 112583 RMVar_ID_112583 Human_SNP_ID_828885226 m1A Human chr17 + 36545680 36545680 36545680 GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA GCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCGGCTGGGAGGAGGTGGTGACGGTGGCAACGGCA A G GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:36545601..36545757 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4420872,Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_9375729,Human_RBP_ID_17890428,Human_RBP_ID_18419578,Human_RBP_ID_22445400 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 112584 RMVar_ID_112584 Human_SNP_ID_828885918 m1A Human chr17 + 81684079 81684079 81684079 GGTTTGGGCTGGAGGTCGCCATGGGGCGAGGCAGCGGCACCTTCGAGCGTCTCCTAGGTAACGCG GGTTTGGGCTGGAGGTCGCCATGGGGCGAGGCGGCGGCACCTTCGAGCGTCTCCTAGGTAACGCG A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:81683976..81684202 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate Human_RBP_ID_238261,Human_RBP_ID_901119,Human_RBP_ID_4465783,Human_RBP_ID_5115274,Human_RBP_ID_5365279,Human_RBP_ID_18419779,Human_RBP_ID_19080429,Human_RBP_ID_20291741,Human_RBP_ID_27838625 Human_Splice_Rec_1881529,Human_Splice_Rec_1881539,Human_Splice_Rec_1881553,Human_Splice_Rec_1881593 112585 RMVar_ID_112585 Human_SNP_ID_828887250 m1A Human chr17 - 18258681 18258681 18258681 GGCCCGGCAGCGAGAGCGGCGCCATGGAGGCCACCGGGGTGCTGCCGTTCGTGCGTGGCGTGGAC GGCCCGGCAGCGAGAGCGGCGCCATGGAGGCCGCCGGGGTGCTGCCGTTCGTGCGTGGCGTGGAC T C FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr17:18258585..18258725;chr17:18258538..18258725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_4409708,Human_RBP_ID_5187114,Human_RBP_ID_9288809 Human_Splice_Rec_1787557,Human_Splice_Rec_1787627,Human_Splice_Rec_1787659,Human_Splice_Rec_1787715,Human_Splice_Rec_1787937,Human_Splice_Rec_1787957,Human_Splice_Rec_1787985,Human_Splice_Rec_1787987 RMVar_hsa_circ_182484,RMVar_hsa_circ_96044 112586 RMVar_ID_112586 Human_SNP_ID_828888318 m1A Human chr17 - 7224016 7224015 7224017 AAACAGCCGAAGAATGTCATTTGTCCCCTCAAAGATCCGGAAGATGCGAAGATCTCGGAGCACAC AAACAGCCGAAGAATGTCATTTGTCCCCTCA__GATCCGGAAGATGCGAAGATCTCGGAGCACAC CTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:7223876..7224025 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 COAD 1 - Human_RBP_ID_13154140,Human_RBP_ID_22806510,Human_RBP_ID_26970247 112587 RMVar_ID_112587 Human_SNP_ID_828894387 m1A Human chr17 - 35151197 35151197 35151197 CGCTGAATTTAAGCATATTTGTCAGCGGAGGAAAAGAAACTAACCAGGATTCCCTCAGTAATGGC CGCTGAATTTAAGCATATTTGTCAGCGGAGGAGAAGAAACTAACCAGGATTCCCTCAGTAATGGC T C RF02543-021 RNACentral:URS000096B15F rRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12165042 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 9 brain Human_RBP_ID_269916,Human_RBP_ID_278128,Human_RBP_ID_487350,Human_RBP_ID_1007430,Human_RBP_ID_1090396,Human_RBP_ID_1181304,Human_RBP_ID_1285759,Human_RBP_ID_1531696,Human_RBP_ID_1855201,Human_RBP_ID_2529294,Human_RBP_ID_3519891,Human_RBP_ID_4419742,Human_RBP_ID_5184461,Human_RBP_ID_5260019,Human_RBP_ID_5275057,Human_RBP_ID_5419990,Human_RBP_ID_5441319,Human_RBP_ID_5466348,Human_RBP_ID_5496861,Human_RBP_ID_5577099,Human_RBP_ID_6584338,Human_RBP_ID_8089712,Human_RBP_ID_8253331,Human_RBP_ID_8449720,Human_RBP_ID_8816443,Human_RBP_ID_9071295,Human_RBP_ID_9257367,Human_RBP_ID_9287242,Human_RBP_ID_9856137,Human_RBP_ID_10483399,Human_RBP_ID_12970319,Human_RBP_ID_17004291,Human_RBP_ID_17063127,Human_RBP_ID_17067912,Human_RBP_ID_17126327,Human_RBP_ID_17190236,Human_RBP_ID_17259153,Human_RBP_ID_17375087,Human_RBP_ID_17490472,Human_RBP_ID_17691782,Human_RBP_ID_17889966,Human_RBP_ID_18179320,Human_RBP_ID_18200129,Human_RBP_ID_18207783,Human_RBP_ID_18291248,Human_RBP_ID_18438752,Human_RBP_ID_18513587,Human_RBP_ID_18530577,Human_RBP_ID_18694818,Human_RBP_ID_20203111,Human_RBP_ID_21889613,Human_RBP_ID_21926904,Human_RBP_ID_22212300,Human_RBP_ID_22422060,Human_RBP_ID_22499210,Human_RBP_ID_22804032,Human_RBP_ID_22949715,Human_RBP_ID_23129097,Human_RBP_ID_23168616,Human_RBP_ID_23275469,Human_RBP_ID_23308812,Human_RBP_ID_23721702,Human_RBP_ID_24478586,Human_RBP_ID_24531813,Human_RBP_ID_25272825,Human_RBP_ID_26449272,Human_RBP_ID_26641589,Human_RBP_ID_26749069,Human_RBP_ID_26959008,Human_RBP_ID_27156494,Human_RBP_ID_27252697,Human_RBP_ID_27451054,Human_RBP_ID_27560927,Human_RBP_ID_27664074 112588 RMVar_ID_112588 Human_SNP_ID_828900306 m1A Human chr17 - 2376154 2376153 2376155 TCCTTGTCTATGCGGTGCAGGTTTAAGGCCACAGTGTCCAGTAATTCTATCTGGAAGAGTGGAGG TCCTTGTCTATGCGGTGCAGGTTTAAGGCCA__GTGTCCAGTAATTCTATCTGGAAGAGTGGAGG CTG C AC006435.2 Ensembl:ENSG00000263345 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:2376151..2376175 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 THCA 1 - 112589 RMVar_ID_112589 Human_SNP_ID_828903109 m1A Human chr17 + 7676144 7676143 7676144 GCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGCAGGGGCCACGGGGGGAGCAGCCTCTGGCATTCT GCAGGGGCCGCCGGTGTAGGAGCTGCTGGTGC_GGGGCCACGGGGGGAGCAGCCTCTGGCATTCT CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7676093..7676225 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 OV 1 - 112590 RMVar_ID_112590 Human_SNP_ID_828905937 m1A Human chr17 - 44210760 44210760 44210760 GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCAGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG GGTCAGGCTGCCTGGCGGAGCGCTGTGCCCCCCGGGGGGCTGCCAGGGCCCCCTCTTCCCCTTGG T G UBTF Ensembl:ENSG00000108312 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44210755..44210886 26863196 MeRIP-seq:(Medium) rs2526011 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,COCA 10 prostate Human_RBP_ID_19082864,Human_RBP_ID_22061384 RMVar_hsa_circ_4823,RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 112591 RMVar_ID_112591 Human_SNP_ID_828906151 m1A Human chr17 - 47696119 47696119 47696119 CGTCAGGATGCTGATGTCGTCCTCGAACATGGACTCCATGGTGAGGGCCGGGCCGCGGCCCACAC CGTCAGGATGCTGATGTCGTCCTCGAACATGGGCTCCATGGTGAGGGCCGGGCCGCGGCCCACAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47696083..47696171 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 112592 RMVar_ID_112592 Human_SNP_ID_828907710 m1A Human chr17 + 42573361 42573361 42573361 CCACTCCTTACAGTACTTCTGCCTCTCTCTGTACACCTAGAAGGAAAAAGCAAGTTCCTCTAACT CCACTCCTTACAGTACTTCTGCCTCTCTCTGTTCACCTAGAAGGAAAAAGCAAGTTCCTCTAACT A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42573006..42573643 26863196 MeRIP-seq:(Medium) rs2292754 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_20215973 112593 RMVar_ID_112593 Human_SNP_ID_828911266 m1A Human chr17 + 48551156 48551156 48551156 CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCACCGCCGCCGCCACCACAGCCCTCTGCTGGATC CCGCTGCCACCACTGCCTCCGCCGCCGCCGCCGCCGCCGCCGCCACCACAGCCCTCTGCTGGATC A G HOXB-AS1,HOXB-AS3 Ensembl:ENSG00000230148,Ensembl:ENSG00000233101 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48551054..48551201 26863196 MeRIP-seq:(Medium) rs559346033 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,large_intestine adenocarcinoma 20 stomach,large intestine Human_RBP_ID_9326712 112594 RMVar_ID_112594 Human_SNP_ID_828919302 m1A Human chr17 - 81510730 81510730 81510730 CCAGCAGATGTGGATTAGCAAGCAGGAGTACGACGAGTCGGGCCCCTCCATCGTCCACCGCAAAT CCAGCAGATGTGGATTAGCAAGCAGGAGTACGGCGAGTCGGGCCCCTCCATCGTCCACCGCAAAT T C ACTG1 Ensembl:ENSG00000184009 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:81510577..81510739;chr17:81510600..81510754 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,UCEC,KIRC,endometrium endometrioid_carcinoma 15 kidney,uterus Human_RBP_ID_49492,Human_RBP_ID_237008,Human_RBP_ID_269872,Human_RBP_ID_502506,Human_RBP_ID_903222,Human_RBP_ID_1544434,Human_RBP_ID_1870689,Human_RBP_ID_3539514,Human_RBP_ID_4458675,Human_RBP_ID_5189183,Human_RBP_ID_5577988,Human_RBP_ID_6651159,Human_RBP_ID_8465864,Human_RBP_ID_8823400,Human_RBP_ID_9076968,Human_RBP_ID_13195009,Human_RBP_ID_17262331,Human_RBP_ID_17494476,Human_RBP_ID_18191018,Human_RBP_ID_18711414,Human_RBP_ID_22223379,Human_RBP_ID_22443234,Human_RBP_ID_22807212,Human_RBP_ID_23754585,Human_RBP_ID_26974447,Human_RBP_ID_27262003,Human_RBP_ID_27458708 Human_miRNA_ID_2391081,Human_miRNA_ID_2391082,Human_miRNA_ID_2592326,Human_miRNA_ID_2592327 RMVar_hsa_circ_94117,RMVar_hsa_circ_78800,RMVar_hsa_circ_105456,RMVar_hsa_circ_127589,RMVar_hsa_circ_82812,RMVar_hsa_circ_123222,RMVar_hsa_circ_187631,RMVar_hsa_circ_187632,RMVar_hsa_circ_187633,RMVar_hsa_circ_187630,RMVar_hsa_circ_95896,RMVar_hsa_circ_187635,RMVar_hsa_circ_187636,RMVar_hsa_circ_187637 112595 RMVar_ID_112595 Human_SNP_ID_828932544 m1A Human chr17 - 76736245 76736245 76736245 AGGTCCCGGTCTCGGTCCAGGAGTCCTCCCCCAGTGTCCAAGAGGGAATCCAAATCCAGGTCGCG AGGTCCCGGTCTCGGTCCAGGAGTCCTCCCCCCGTGTCCAAGAGGGAATCCAAATCCAGGTCGCG T G SRSF2 Ensembl:ENSG00000161547 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:76736175..76736900 26863196 MeRIP-seq:(Medium) rs1283104650 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_48773,Human_RBP_ID_500797,Human_RBP_ID_821284,Human_RBP_ID_903694,Human_RBP_ID_1010718,Human_RBP_ID_1543077,Human_RBP_ID_3537950,Human_RBP_ID_4479323,Human_RBP_ID_6646654,Human_RBP_ID_9376907,Human_RBP_ID_13175181,Human_RBP_ID_17901445,Human_RBP_ID_22059663,Human_RBP_ID_22806954,Human_RBP_ID_25326902,Human_RBP_ID_26330892,Human_RBP_ID_26972184,Human_RBP_ID_27260279 Human_Splice_Rec_1872427,Human_Splice_Rec_1872433,Human_Splice_Rec_1872437,Human_Splice_Rec_1872445,Human_Splice_Rec_1872457 Human_miRNA_ID_2956442 RMVar_hsa_circ_187247,RMVar_hsa_circ_114043,RMVar_hsa_circ_90518,RMVar_hsa_circ_187246 112596 RMVar_ID_112596 Human_SNP_ID_828936770 m1A Human chr17 - 8143718 8143718 8143718 CACCCTCCACCCCCTGGCCCACCCCACCAGCCACTACCCCCTTCCCAGCGGTTGTCCAGCCCTAC CACCCTCCACCCCCTGGCCCACCCCACCAGCCCCTACCCCCTTCCCAGCGGTTGTCCAGCCCTAC T G PER1 Ensembl:ENSG00000179094 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:8143623..8143811 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_503681,Human_RBP_ID_17079478,Human_RBP_ID_17566356,Human_RBP_ID_18941375 112597 RMVar_ID_112597 Human_SNP_ID_828938225 m1A Human chr17 + 44960366 44960366 44960366 GGTCCGCGTCCTGGGCAATAGCACTGGCCCGCACCTGCGGGTGGGGGACACGGGAGGGAGGGCGA GGTCCGCGTCCTGGGCAATAGCACTGGCCCGCGCCTGCGGGTGGGGGACACGGGAGGGAGGGCGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:44960140..44967474 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 112598 RMVar_ID_112598 Human_SNP_ID_828940815 m1A Human chr17 - 58007129 58007128 58007129 GAGTCCGCGCTTTTCGTCACCGCCATGTCGGGAGGTGGTGTGATTCGTGGCCCCGCAGGGAACAA GAGTCCGCGCTTTTCGTCACCGCCATGTCGGG_GGTGGTGTGATTCGTGGCCCCGCAGGGAACAA CT C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:58007008..58007308 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 CLLE 1 - Human_RBP_ID_236262,Human_RBP_ID_495298,Human_RBP_ID_765369,Human_RBP_ID_902547,Human_RBP_ID_1538264,Human_RBP_ID_1864031,Human_RBP_ID_3530020,Human_RBP_ID_4441189,Human_RBP_ID_6619719,Human_RBP_ID_9074147,Human_RBP_ID_9326760,Human_RBP_ID_9378642,Human_RBP_ID_13093569,Human_RBP_ID_17897080,Human_RBP_ID_18419670,Human_RBP_ID_18703722,Human_RBP_ID_22061541,Human_RBP_ID_22218055,Human_RBP_ID_22805882,Human_RBP_ID_23129486,Human_RBP_ID_23738262,Human_RBP_ID_26967271 Human_miRNA_ID_2016950 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616 112599 RMVar_ID_112599 Human_SNP_ID_828945347 m1A Human chr17 - 7675149 7675143 7675150 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGG_______GTCCGCGCCATGGCCATCTACAAGCAG CGCGGGTG C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..38 33 BLCA 1 - Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112600 RMVar_ID_112600 Human_SNP_ID_828951326 m1A Human chr17 - 7236160 7236160 7236160 AGACTCTGAAGAGGAGGAGGAAGAGGAGGAAGAGGAAGAAGAAGAAGAGATGGCAACAGTGGTAG AGACTCTGAAGAGGAGGAGGAAGAGGAGGAAGGGGAAGAAGAAGAAGAGATGGCAACAGTGGTAG T C PHF23 Ensembl:ENSG00000040633 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7236110..7236210 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 5 biliary tract,gallbladder Human_RBP_ID_201529,Human_RBP_ID_4448818,Human_RBP_ID_9375253,Human_RBP_ID_24544767,Human_RBP_ID_26330642 112601 RMVar_ID_112601 Human_SNP_ID_828951508 m1A Human chr17 + 7893856 7893856 7893856 GAGTAAGAGCCCCCGAGTGCCTGATGGACGCAAGAAGCTTCGGGGAAAGAAAATGGCACCACTCA GAGTAAGAGCCCCCGAGTGCCTGATGGACGCATGAAGCTTCGGGGAAAGAAAATGGCACCACTCA A T CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7893806..7893949 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_8465063,Human_RBP_ID_26331219 Human_Splice_Rec_1774930,Human_Splice_Rec_1774931,Human_Splice_Rec_1775008,Human_Splice_Rec_1775009,Human_Splice_Rec_1775020,Human_Splice_Rec_1775021,Human_Splice_Rec_1775072,Human_Splice_Rec_1775073,Human_Splice_Rec_1775150,Human_Splice_Rec_1775151,Human_Splice_Rec_1775226,Human_Splice_Rec_1775227,Human_Splice_Rec_1775240,Human_Splice_Rec_1775241,Human_Splice_Rec_1775245 112602 RMVar_ID_112602 Human_SNP_ID_828966767 m1A Human chr17 + 82237657 82237657 82237657 GGGGCTTGGGAAGGTGCGGCCCTACTCCGTCTACCTCTTCAGCTTCTCCATGTTCTTCAACGGCC GGGGCTTGGGAAGGTGCGGCCCTACTCCGTCTGCCTCTTCAGCTTCTCCATGTTCTTCAACGGCC A G SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:82237217..82237736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_48556,Human_RBP_ID_22761837,Human_RBP_ID_24416237,Human_RBP_ID_27459342 Human_miRNA_ID_1915100,Human_miRNA_ID_1917549,Human_miRNA_ID_1920001,Human_miRNA_ID_1922460,Human_miRNA_ID_1924914,Human_miRNA_ID_1927365,Human_miRNA_ID_1929814,Human_miRNA_ID_1932265,Human_miRNA_ID_2464349,Human_miRNA_ID_2561202,Human_miRNA_ID_2630090,Human_miRNA_ID_2643204,Human_miRNA_ID_3125950 RMVar_hsa_circ_13571,RMVar_hsa_circ_187919,RMVar_hsa_circ_312414 112603 RMVar_ID_112603 Human_SNP_ID_828969643 m1A Human chr17 + 43209941 43209941 43209941 TTCTGAAGATCAGACAGCAGCCCTGATGGCCCATCTCTTTGAAATGGGATTCTGTGACAGGCAGC TTCTGAAGATCAGACAGCAGCCCTGATGGCCCGTCTCTTTGAAATGGGATTCTGTGACAGGCAGC A G NBR1 Ensembl:ENSG00000188554 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8482 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_9378294,Human_RBP_ID_22499543 Human_Splice_Rec_1823020,Human_Splice_Rec_1823058,Human_Splice_Rec_1823098 112604 RMVar_ID_112604 Human_SNP_ID_828972053 m1A Human chr17 - 42950663 42950663 42950663 GAAGAAAGGCCGTTTTCAGGGCAAGGCCACCAAGATGAGCCGGCGGATGGAGGCGCAGGCGCTTC GAAGAAAGGCCGTTTTCAGGGCAAGGCCACCAGGATGAGCCGGCGGATGGAGGCGCAGGCGCTTC T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding exon,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:42950614..42950778 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 5 stomach Human_RBP_ID_4428987,Human_RBP_ID_13012713,Human_RBP_ID_22061365 Human_Splice_Rec_1821708,Human_Splice_Rec_1821712,Human_Splice_Rec_1821716,Human_Splice_Rec_1821720,Human_Splice_Rec_1821728,Human_Splice_Rec_1821750,Human_Splice_Rec_1821876,Human_Splice_Rec_1821910,Human_Splice_Rec_1821940,Human_Splice_Rec_1821972 112605 RMVar_ID_112605 Human_SNP_ID_828976237 m1A Human chr17 + 59237256 59237256 59237256 CCCCATCTCTAGAAAATGCACAAAAAAAATTAACCGGGCGTGGTGGTGCAAGCTGTAGTCACAGC CCCCATCTCTAGAAAATGCACAAAAAAAATTACCCGGGCGTGGTGGTGCAAGCTGTAGTCACAGC A C GDPD1 Ensembl:ENSG00000153982 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:59237133..59237260 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_38503,RMVar_hsa_circ_33114 112606 RMVar_ID_112606 Human_SNP_ID_828990580 m1A Human chr17 - 16492038 16492038 16492038 ACGGGCGGCCGAGGGGCGGGCGGTTGGCGGGGACGCGGCCTCGCGGCCCAGAGCGGAGAGTCCCG ACGGGCGGCCGAGGGGCGGGCGGTTGGCGGGGGCGCGGCCTCGCGGCCCAGAGCGGAGAGTCCCG T C LRRC75A Ensembl:ENSG00000181350 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16491768..16492079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112607 RMVar_ID_112607 Human_SNP_ID_828993397 m1A Human chr17 + 50185977 50185977 50185977 CGGTGGACATCAGGCGCAGGAAGGTCAGCTGGATGGCCACATCGGCAGGGTCGGAGCCCTGGCCG CGGTGGACATCAGGCGCAGGAAGGTCAGCTGGTTGGCCACATCGGCAGGGTCGGAGCCCTGGCCG A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:50185926..50186000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 112608 RMVar_ID_112608 Human_SNP_ID_829005493 m1A Human chr17 + 63751928 63751928 63751928 TCCTTACAAATCGTAGTTTTACCCCAGTGATAAGTTTGTCTAACCTCCAGCCTGCGCTGTTTCTC TCCTTACAAATCGTAGTTTTACCCCAGTGATACGTTTGTCTAACCTCCAGCCTGCGCTGTTTCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63751926..63752049 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - 112609 RMVar_ID_112609 Human_SNP_ID_829005577 m1A Human chr17 - 19745136 19745136 19745136 CCCTCAGCCAGCTGCAGGTGCTCTCTGTCCCCAGGCGCCATGAGCAAGATCAGCGAGGCCGTGAA CCCTCAGCCAGCTGCAGGTGCTCTCTGTCCCCGGGCGCCATGAGCAAGATCAGCGAGGCCGTGAA T C ALDH3A1 Ensembl:ENSG00000108602 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:19745116..19745431 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - 112610 RMVar_ID_112610 Human_SNP_ID_829008400 m1A Human chr17 - 42698756 42698756 42698756 GGGTGGGGACCTGGGCAGGGCCTGAAGTGGGTAGGGGAGGTTTGCTGCCAGGATGGTACTCGTGG GGGTGGGGACCTGGGCAGGGCCTGAAGTGGGTGGGGGAGGTTTGCTGCCAGGATGGTACTCGTGG T C AC100793.3 Ensembl:ENSG00000267765 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42698706..42698924 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_200554 112611 RMVar_ID_112611 Human_SNP_ID_829008654 m1A Human chr17 + 5000338 5000338 5000338 CAGCCAGGATGCCAAGTGTGTGGTCAGCATGCAGGGCAACACCACCTGTGAGTGAGTCCCCGGGG CAGCCAGGATGCCAAGTGTGTGGTCAGCATGCGGGGCAACACCACCTGTGAGTGAGTCCCCGGGG A G KIF1C Ensembl:ENSG00000129250 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4998047..5000825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_4464265,Human_RBP_ID_18702312 Human_Splice_Rec_1766051,Human_Splice_Rec_1766097 Human_miRNA_ID_864794,Human_miRNA_ID_2381286,Human_miRNA_ID_3024295,Human_miRNA_ID_3091074 RMVar_hsa_circ_80301,RMVar_hsa_circ_60505,RMVar_hsa_circ_102051,RMVar_hsa_circ_44265,RMVar_hsa_circ_181574,RMVar_hsa_circ_181575 112612 RMVar_ID_112612 Human_SNP_ID_829014391 m1A Human chr17 + 45115443 45115443 45115443 CGATCCGACAGAGCCCGGCCATCCTCGCTCCGAGCAGCGGGCAACTTCTTTCCCTTCACCAGGAC CGATCCGACAGAGCCCGGCCATCCTCGCTCCGTGCAGCGGGCAACTTCTTTCCCTTCACCAGGAC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:45115426..45115450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 112613 RMVar_ID_112613 Human_SNP_ID_829015966 m1A Human chr17 + 747311 747311 747311 TCCTCTGTCAGCGCAAACACAGTCAGCATGTCAGCCAGGTTGGCCAGCGCACAGCACTTCCTCCC TCCTCTGTCAGCGCAAACACAGTCAGCATGTCTGCCAGGTTGGCCAGCGCACAGCACTTCCTCCC A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:747262..747540 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112614 RMVar_ID_112614 Human_SNP_ID_829016531 m1A Human chr17 - 38853699 38853699 38853699 TTCTTTTTTCCGGCGTTCAAGATGTCGAAGCGAGGTGAGGTTTTGTTTCTGGAGGATCCTCCACC TTCTTTTTTCCGGCGTTCAAGATGTCGAAGCGGGGTGAGGTTTTGTTTCTGGAGGATCCTCCACC T C RPL23 Ensembl:ENSG00000125691 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:38853676..38853725 26863196 MeRIP-seq:(Medium) rs531763616 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_237764,Human_RBP_ID_488234,Human_RBP_ID_768415,Human_RBP_ID_1532889,Human_RBP_ID_1856822,Human_RBP_ID_4423106,Human_RBP_ID_12990810,Human_RBP_ID_17654154,Human_RBP_ID_17904824,Human_RBP_ID_22212975,Human_RBP_ID_22807898,Human_RBP_ID_23169019,Human_RBP_ID_24415187,Human_RBP_ID_24481882,Human_RBP_ID_26460483 Human_Splice_Rec_1810177,Human_Splice_Rec_1810185,Human_Splice_Rec_1810195,Human_Splice_Rec_1810211,Human_Splice_Rec_1810215,Human_Splice_Rec_1810233 112615 RMVar_ID_112615 Human_SNP_ID_829019108 m1A Human chr17 + 82584187 82584187 82584187 ATCCAGGAAGCCCGGTTTGCCCAGAGCGCCCCAGGTGAGACAGCGGGAGAGGAAGCGAGGGCCCC ATCCAGGAAGCCCGGTTTGCCCAGAGCGCCCCGGGTGAGACAGCGGGAGAGGAAGCGAGGGCCCC A G FOXK2 Ensembl:ENSG00000141568 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82584138..82585984 32194978 MeRIP-seq:(Medium) rs1180214440 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_904157,Human_RBP_ID_18470316 Human_Splice_Rec_1886151,Human_Splice_Rec_1886169,Human_Splice_Rec_1886205 RMVar_hsa_circ_2831,RMVar_hsa_circ_86420,RMVar_hsa_circ_267415,RMVar_hsa_circ_187964,RMVar_hsa_circ_76945,RMVar_hsa_circ_187963,RMVar_hsa_circ_281876,RMVar_hsa_circ_311160,RMVar_hsa_circ_359641,RMVar_hsa_circ_187965,RMVar_hsa_circ_187966,RMVar_hsa_circ_108301,RMVar_hsa_circ_20959,RMVar_hsa_circ_121923,RMVar_hsa_circ_187971,RMVar_hsa_circ_274499,RMVar_hsa_circ_301071,RMVar_hsa_circ_187972,RMVar_hsa_circ_187973,RMVar_hsa_circ_187974,RMVar_hsa_circ_277266,RMVar_hsa_circ_347737,RMVar_hsa_circ_187975 112616 RMVar_ID_112616 Human_SNP_ID_829021757 m1A Human chr17 - 49413267 49413267 49413267 CCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAACATGGCTGCCAAAGTGTTTGAGTCCATTGGC CCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGACACATGGCTGCCAAAGTGTTTGAGTCCATTGGC T G PHB Ensembl:ENSG00000167085 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:49413144..49414875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas Human_RBP_ID_236573,Human_RBP_ID_903588,Human_RBP_ID_4466565,Human_RBP_ID_5114751,Human_RBP_ID_5364541,Human_RBP_ID_9327351,Human_RBP_ID_17654261,Human_RBP_ID_22445593,Human_RBP_ID_23210031 Human_Splice_Rec_1835730,Human_Splice_Rec_1835731,Human_Splice_Rec_1835744,Human_Splice_Rec_1835745,Human_Splice_Rec_1835756,Human_Splice_Rec_1835757,Human_Splice_Rec_1835764,Human_Splice_Rec_1835765,Human_Splice_Rec_1835780,Human_Splice_Rec_1835781,Human_Splice_Rec_1835792,Human_Splice_Rec_1835793,Human_Splice_Rec_1835803,Human_Splice_Rec_1835811,Human_Splice_Rec_1835820,Human_Splice_Rec_1835821,Human_Splice_Rec_1835830,Human_Splice_Rec_1835831,Human_Splice_Rec_1835844,Human_Splice_Rec_1835845,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 112617 RMVar_ID_112617 Human_SNP_ID_829022141 m1A Human chr17 - 80217142 80217142 80217142 AGAGTGGCGCGTACAACAACAGCGCCATCGCCACCCCGCACCTGGACGCCTTGGCCCGCCGCAGC AGAGTGGCGCGTACAACAACAGCGCCATCGCCCCCCCGCACCTGGACGCCTTGGCCCGCCGCAGC T G SGSH Ensembl:ENSG00000181523 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80217091..80217175 26863196 MeRIP-seq:(Medium) rs962142186 Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 2 breast Human_RBP_ID_27458375 Human_Splice_Rec_1878126,Human_Splice_Rec_1878140,Human_Splice_Rec_1878148,Human_Splice_Rec_1878164,Human_Splice_Rec_1878176,Human_Splice_Rec_1878184,Human_Splice_Rec_1878194,Human_Splice_Rec_1878202,Human_Splice_Rec_1878208,Human_Splice_Rec_1878216,Human_Splice_Rec_1878224,Human_Splice_Rec_1878230,Human_Splice_Rec_1878234 RMVar_hsa_circ_75752,RMVar_hsa_circ_187470 112618 RMVar_ID_112618 Human_SNP_ID_829025292 m1A Human chr17 + 413792 413792 413792 ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACACTGACCCCGAGGCCCTCAAGGGCTTCCACCCC ACCCCGACCCCAAGGCCCTCAAGGGTTTCCACCCTGACCCCGAGGCCCTCAAGGGCTTCCACCCC A C C17orf97 Ensembl:ENSG00000187624 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:413672..414021 26863196 MeRIP-seq:(Medium) rs782653538 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 5 large intestine,haematopoietic and lymphoid tissue 112619 RMVar_ID_112619 Human_SNP_ID_829031531 m1A Human chr17 - 80250057 80250057 80250057 GCAGTGCTCAGAAGGCTCCTAGGTGAGGCCTAAGACGCAGGGCCTGGGACCCAGCCCTTACACTT GCAGTGCTCAGAAGGCTCCTAGGTGAGGCCTAGGACGCAGGGCCTGGGACCCAGCCCTTACACTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80250021..80250105 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112620 RMVar_ID_112620 Human_SNP_ID_829047163 m1A Human chr17 - 82443961 82443961 82443961 GTGCCTGAGCCCGTGCACCGCCCACAGGACCCATGGCACATTCCCGGTGTGCCTGAGCCCGTGCA GTGCCTGAGCCCGTGCACCGCCCACAGGACCCGTGGCACATTCCCGGTGTGCCTGAGCCCGTGCA T C CYBC1 Ensembl:ENSG00000178927 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11557531 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,liver neoplasm,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 73 liver,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_18712600,Human_RBP_ID_27263277,Human_RBP_ID_27459541 Human_miRNA_ID_1934057,Human_miRNA_ID_2197863,Human_miRNA_ID_2658892,Human_miRNA_ID_2936874 RMVar_hsa_circ_89549,RMVar_hsa_circ_94847,RMVar_hsa_circ_187945,RMVar_hsa_circ_187946 112621 RMVar_ID_112621 Human_SNP_ID_829055276 m1A Human chr17 + 2362202 2362202 2362202 CCGGCCCTCAGCCCTCAGGCCTTGAAACACGTATGGGTACGCACGGCGCTCATCGAGAAAGTTCT CCGGCCCTCAGCCCTCAGGCCTTGAAACACGTGTGGGTACGCACGGCGCTCATCGAGAAAGTTCT A G SGSM2 Ensembl:ENSG00000141258 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:2362064..2362205 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_4412069 Human_Splice_Rec_1759748,Human_Splice_Rec_1759754,Human_Splice_Rec_1759755,Human_Splice_Rec_1759800,Human_Splice_Rec_1759801,Human_Splice_Rec_1759816,Human_Splice_Rec_1759817,Human_Splice_Rec_1759860,Human_Splice_Rec_1759861,Human_Splice_Rec_1759900,Human_Splice_Rec_1759901 RMVar_hsa_circ_13788,RMVar_hsa_circ_87299,RMVar_hsa_circ_94930,RMVar_hsa_circ_181233,RMVar_hsa_circ_78841,RMVar_hsa_circ_181234,RMVar_hsa_circ_181235 112622 RMVar_ID_112622 Human_SNP_ID_829055531 m1A Human chr17 - 28744114 28744114 28744114 GCTTCTCCAGGAACTTGTAGTCGAAGCCAGGCATGGCGGGCGAGCGGCCGGCACGGGCGAGCGGG GCTTCTCCAGGAACTTGTAGTCGAAGCCAGGCGTGGCGGGCGAGCGGCCGGCACGGGCGAGCGGG T C RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr17:28744027..28744114 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 112623 RMVar_ID_112623 Human_SNP_ID_829059482 m1A Human chr17 + 2701516 2701516 2701516 ATCCGCTCATGGTGAGTACTTTCAGGCACTGCAAGGGCTTCGGGAGCGGCCGAGTCTGAGGGGCC ATCCGCTCATGGTGAGTACTTTCAGGCACTGCTAGGGCTTCGGGAGCGGCCGAGTCTGAGGGGCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:2701365..2701752 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 112624 RMVar_ID_112624 Human_SNP_ID_829063989 m1A Human chr17 - 7503777 7503777 7503777 GAAGAGCACAACACTCACAATGGCTTGGTTGAACTTGGACTCAATCTCCCCAAGCAGCCAGTCGA GAAGAGCACAACACTCACAATGGCTTGGTTGAGCTTGGACTCAATCTCCCCAAGCAGCCAGTCGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7503601..7503815 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 112625 RMVar_ID_112625 Human_SNP_ID_829069660 m1A Human chr17 - 79081058 79081058 79081058 CCTGTCTGCAGGCTCACCTGTTGTGCTGGTTGAGTTCGTCTTGCCATTTGAGCTGCCCACTTTGC CCTGTCTGCAGGCTCACCTGTTGTGCTGGTTGGGTTCGTCTTGCCATTTGAGCTGCCCACTTTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:79080988..79081106 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 112626 RMVar_ID_112626 Human_SNP_ID_829076142 m1A Human chr17 - 21284902 21284902 21284902 GCGGGCGACTCCATGCTGCAAGTGGGTCCTGGACGGCGGTGGAGACTAATCTAGAGGACTGCGGG GCGGGCGACTCCATGCTGCAAGTGGGTCCTGGGCGGCGGTGGAGACTAATCTAGAGGACTGCGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:21284851..21287992 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 112627 RMVar_ID_112627 Human_SNP_ID_829077160 m1A Human chr17 + 61405391 61405391 61405391 GAGGGGCAAGGAGCCGGCCGAGAGCGGCGGGGACGGCCCGTTCGGCCTGAGGAGCCTGGAGAAGG GAGGGGCAAGGAGCCGGCCGAGAGCGGCGGGGGCGGCCCGTTCGGCCTGAGGAGCCTGGAGAAGG A G TBX2 Ensembl:ENSG00000121068 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:61405341..61405417 26863196 MeRIP-seq:(Medium) rs1195162033 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 1 head and neck Human_RBP_ID_22959880 RMVar_hsa_circ_94758,RMVar_hsa_circ_186029 112628 RMVar_ID_112628 Human_SNP_ID_829085172 m1A Human chr17 + 4956074 4956074 4956074 CACCAACCCCAAGAGGATTGCCCAGGCCGTTGAGAAGAAGGCCTGCAACTGTCTGCTGCTGAAGG CACCAACCCCAAGAGGATTGCCCAGGCCGTTGTGAAGAAGGCCTGCAACTGTCTGCTGCTGAAGG A T ENO3 Ensembl:ENSG00000108515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:4956023..4956095 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_9375179,Human_RBP_ID_18990183 Human_Splice_Rec_1765503,Human_Splice_Rec_1765559,Human_Splice_Rec_1765579,Human_Splice_Rec_1765599,Human_Splice_Rec_1765605 RMVar_hsa_circ_105693,RMVar_hsa_circ_181567 112629 RMVar_ID_112629 Human_SNP_ID_829090199 m1A Human chr17 - 28655401 28655401 28655401 AGTTACTGGAGGATACGGGGGAAGAGTGCCACAGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG AGTTACTGGAGGATACGGGGGAAGAGTGCCACTGTGTGTGAGAGGGGAACCCCCATCAAGTGTGG T A SDF2 Ensembl:ENSG00000132581 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:28655351..28655517 32194978 MeRIP-seq:(Medium) rs746151655 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_5115097,Human_RBP_ID_17654618,Human_RBP_ID_18692596,Human_RBP_ID_22443545,Human_RBP_ID_22760737 Human_Splice_Rec_1796418,Human_Splice_Rec_1796424,Human_Splice_Rec_1796428,Human_Splice_Rec_1796434,Human_Splice_Rec_1796440,Human_Splice_Rec_1796448 RMVar_hsa_circ_182959,RMVar_hsa_circ_291816,RMVar_hsa_circ_182960,RMVar_hsa_circ_331244 112630 RMVar_ID_112630 Human_SNP_ID_829091116 m1A Human chr17 + 40417867 40417867 40417867 ACAGGCAGGACCCCACGAGACCACCCCCGACCAAGCCGCTTCTCCACAGACGCGCGTCGGTTAGG ACAGGCAGGACCCCACGAGACCACCCCCGACCGAGCCGCTTCTCCACAGACGCGCGTCGGTTAGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:40417739..40417925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 MESO 1 - 112631 RMVar_ID_112631 Human_SNP_ID_829091765 m1A Human chr17 - 17509525 17509525 17509525 CCTCATCCACAGGTGATTACTTCGGGATCCTCAAGGAGGCGAGAGTGACCGTGTTCCCCTTCAAC CCTCATCCACAGGTGATTACTTCGGGATCCTCGAGGAGGCGAGAGTGACCGTGTTCCCCTTCAAC T C PEMT Ensembl:ENSG00000133027 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:17509451..17509525 32194978 MeRIP-seq:(Medium) rs761000841 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_484247,Human_RBP_ID_1006499,Human_RBP_ID_17886249,Human_RBP_ID_26813219 Human_Splice_Rec_1785598,Human_Splice_Rec_1785599,Human_Splice_Rec_1785606,Human_Splice_Rec_1785607,Human_Splice_Rec_1785618,Human_Splice_Rec_1785619,Human_Splice_Rec_1785630,Human_Splice_Rec_1785631,Human_Splice_Rec_1785642,Human_Splice_Rec_1785643,Human_Splice_Rec_1785656,Human_Splice_Rec_1785657,Human_Splice_Rec_1785668,Human_Splice_Rec_1785669,Human_Splice_Rec_1785682,Human_Splice_Rec_1785683,Human_Splice_Rec_1785694,Human_Splice_Rec_1785695,Human_Splice_Rec_1785702 RMVar_hsa_circ_19370 112632 RMVar_ID_112632 Human_SNP_ID_829099149 m1A Human chr17 + 7906955 7906955 7906955 GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGAGCCTCCTCTCCTACCAAAACGTCTCCCACCAC GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGGGCCTCCTCTCCTACCAAAACGTCTCCCACCAC A G CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7906904..7907000 26863196 MeRIP-seq:(Medium) rs1156230891 Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_131738,Human_RBP_ID_2524984 Human_Splice_Rec_1774978,Human_Splice_Rec_1774979,Human_Splice_Rec_1775120,Human_Splice_Rec_1775121,Human_Splice_Rec_1775198,Human_Splice_Rec_1775199,Human_Splice_Rec_1775264,Human_Splice_Rec_1775265 Human_miRNA_ID_881101,Human_miRNA_ID_1035780,Human_miRNA_ID_1395521,Human_miRNA_ID_1546930,Human_miRNA_ID_2793519 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953,RMVar_hsa_circ_109671,RMVar_hsa_circ_87683,RMVar_hsa_circ_181963,RMVar_hsa_circ_119752,RMVar_hsa_circ_181964,RMVar_hsa_circ_181965,RMVar_hsa_circ_88217,RMVar_hsa_circ_181969,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 112633 RMVar_ID_112633 Human_SNP_ID_829099159 m1A Human chr17 + 7906955 7906955 7906955 GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGAGCCTCCTCTCCTACCAAAACGTCTCCCACCAC GACCCCAGCGCCGATTCTAAGCGCTCCTCCAGCGCCTCCTCTCCTACCAAAACGTCTCCCACCAC A C CHD3 Ensembl:ENSG00000170004 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7906904..7907000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_131738,Human_RBP_ID_2524984 Human_Splice_Rec_1774978,Human_Splice_Rec_1774979,Human_Splice_Rec_1775120,Human_Splice_Rec_1775121,Human_Splice_Rec_1775198,Human_Splice_Rec_1775199,Human_Splice_Rec_1775264,Human_Splice_Rec_1775265 Human_miRNA_ID_881101,Human_miRNA_ID_1035780,Human_miRNA_ID_1395521,Human_miRNA_ID_1546930,Human_miRNA_ID_2793519 RMVar_hsa_circ_115206,RMVar_hsa_circ_181951,RMVar_hsa_circ_112359,RMVar_hsa_circ_107773,RMVar_hsa_circ_76284,RMVar_hsa_circ_181954,RMVar_hsa_circ_181955,RMVar_hsa_circ_181953,RMVar_hsa_circ_109671,RMVar_hsa_circ_87683,RMVar_hsa_circ_181963,RMVar_hsa_circ_119752,RMVar_hsa_circ_181964,RMVar_hsa_circ_181965,RMVar_hsa_circ_88217,RMVar_hsa_circ_181969,RMVar_hsa_circ_181977,RMVar_hsa_circ_106058 112634 RMVar_ID_112634 Human_SNP_ID_829102126 m1A Human chr17 - 82086255 82086255 82086255 GAACATGCCCAGCCTGAAGATGAAGGTGGTGGAGGTGGGTGCCTCCTGGGCAGCCAGGCCTCTGC GAACATGCCCAGCCTGAAGATGAAGGTGGTGGGGGTGGGTGCCTCCTGGGCAGCCAGGCCTCTGC T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:82086251..82086275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,cerebrum astrocytoma_Grade_IV 2 brain Human_RBP_ID_3951491,Human_RBP_ID_9290460,Human_RBP_ID_18989723,Human_RBP_ID_19080683 Human_Splice_Rec_1884405 RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_113795,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187862,RMVar_hsa_circ_107932,RMVar_hsa_circ_101410,RMVar_hsa_circ_118347,RMVar_hsa_circ_76836,RMVar_hsa_circ_187864,RMVar_hsa_circ_187865,RMVar_hsa_circ_90074,RMVar_hsa_circ_79716,RMVar_hsa_circ_187869,RMVar_hsa_circ_187870,RMVar_hsa_circ_105832,RMVar_hsa_circ_264990,RMVar_hsa_circ_187871,RMVar_hsa_circ_51662,RMVar_hsa_circ_113373,RMVar_hsa_circ_187872,RMVar_hsa_circ_104196,RMVar_hsa_circ_187873,RMVar_hsa_circ_187874 112635 RMVar_ID_112635 Human_SNP_ID_829103471 m1A Human chr17 + 82738639 82738639 82738639 TGATGGAGCATTTGAAGATGAAGAGCTTGAGCAGGTGAGTGTGTGTGAGACCCATATGCGCACAT TGATGGAGCATTTGAAGATGAAGAGCTTGAGCGGGTGAGTGTGTGTGAGACCCATATGCGCACAT A G FN3K Ensembl:ENSG00000167363 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82738589..82740861 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_897170,Human_RBP_ID_3547853,Human_RBP_ID_4467430,Human_RBP_ID_9377197,Human_RBP_ID_9424504,Human_RBP_ID_18989788,Human_RBP_ID_26334019 Human_Splice_Rec_1886477,Human_Splice_Rec_1886487,Human_Splice_Rec_1886491,Human_Splice_Rec_1886497 RMVar_hsa_circ_45152,RMVar_hsa_circ_359400 112636 RMVar_ID_112636 Human_SNP_ID_829103608 m1A Human chr17 + 47683352 47683352 47683352 TCTGGCGTTAGAGGATATAGAAAAATATAAGTACAATTGTTACAAATAACGCAGACTTCAAAAAC TCTGGCGTTAGAGGATATAGAAAAATATAAGTGCAATTGTTACAAATAACGCAGACTTCAAAAAC A G KPNB1 Ensembl:ENSG00000108424 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:47683301..47683400;chr17:47683301..47683487 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_491970,Human_RBP_ID_1008711,Human_RBP_ID_1287019,Human_RBP_ID_1535866,Human_RBP_ID_1861083,Human_RBP_ID_2529770,Human_RBP_ID_3526545,Human_RBP_ID_6605852,Human_RBP_ID_8191177,Human_RBP_ID_9073009,Human_RBP_ID_13049633,Human_RBP_ID_17260258,Human_RBP_ID_17376074,Human_RBP_ID_17491829,Human_RBP_ID_17582586,Human_RBP_ID_18293157,Human_RBP_ID_22805157,Human_RBP_ID_22952963,Human_RBP_ID_23731404,Human_RBP_ID_26452378,Human_RBP_ID_26643106,Human_RBP_ID_27255711 RMVar_hsa_circ_99626,RMVar_hsa_circ_185004,RMVar_hsa_circ_126447,RMVar_hsa_circ_185012 112637 RMVar_ID_112637 Human_SNP_ID_829105956 m1A Human chr17 - 82415531 82415531 82415531 GCGGGCCTGGGGGCTGGCTTTGTGCTCACCGCACTCCTGCTCTGGAGCAGCTTGGGGGCCGACGA GCGGGCCTGGGGGCTGGCTTTGTGCTCACCGCGCTCCTGCTCTGGAGCAGCTTGGGGGCCGACGA T C OGFOD3 Ensembl:ENSG00000181396 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82415480..82415579 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 2 head and neck Human_RBP_ID_4465008,Human_RBP_ID_22444156 Human_Splice_Rec_1885206,Human_Splice_Rec_1885224,Human_Splice_Rec_1885256,Human_Splice_Rec_1885298,Human_Splice_Rec_1885312 Human_miRNA_ID_2253275,Human_miRNA_ID_2825950,Human_miRNA_ID_2859923 RMVar_hsa_circ_24366,RMVar_hsa_circ_118624,RMVar_hsa_circ_187939 112638 RMVar_ID_112638 Human_SNP_ID_829105968 m1A Human chr17 + 19248867 19248867 19248867 GTTTAGAAAGTGGTGTCAGACACTAGAATGGAACCTGGGAACCAGAGAAGGCTTCGAGGAAATAG GTTTAGAAAGTGGTGTCAGACACTAGAATGGACCCTGGGAACCAGAGAAGGCTTCGAGGAAATAG A C EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:19248865..19248956 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_12917403 RMVar_hsa_circ_182564,RMVar_hsa_circ_110734,RMVar_hsa_circ_119994,RMVar_hsa_circ_182565 112639 RMVar_ID_112639 Human_SNP_ID_829112796 m1A Human chr17 - 47071559 47071559 47071559 CAGGTCAAGGAAGTTCCTGAGGTCCCAGGGCTAATAAGTGGCCTGACTCCACCACCAGCCCCCAG CAGGTCAAGGAAGTTCCTGAGGTCCCAGGGCTGATAAGTGGCCTGACTCCACCACCAGCCCCCAG T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:47071552..47071681 32194978 MeRIP-seq:(Medium) rs552652915 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_Splice_Rec_1831492,Human_Splice_Rec_1831496 RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846,RMVar_hsa_circ_184889,RMVar_hsa_circ_104255 112640 RMVar_ID_112640 Human_SNP_ID_829113622 m1A Human chr17 + 82028665 82028665 82028665 AGAAGATGCAGACAGAGCCTGGAGGACTCCGAAAGCCTGCGCATCAAGGAGGTGCCCTCTTCGTT AGAAGATGCAGACAGAGCCTGGAGGACTCCGATAGCCTGCGCATCAAGGAGGTGCCCTCTTCGTT A T LRRC45 Ensembl:ENSG00000169683 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:82028589..82028719 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_901200,Human_RBP_ID_9377139,Human_RBP_ID_18989651,Human_RBP_ID_22959974,Human_RBP_ID_27814393 Human_Splice_Rec_1883508,Human_Splice_Rec_1883509,Human_Splice_Rec_1883542,Human_Splice_Rec_1883554,Human_Splice_Rec_1883555 112641 RMVar_ID_112641 Human_SNP_ID_829120279 m1A Human chr17 + 5109766 5109766 5109766 CCCATCATCATCATCTTCTCTTGTCCCTGTGTACCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG CCCATCATCATCATCTTCTCTTGTCCCTGTGTGCCCTGAAGGGCCAGAGTTTCAGCTGCTGTTAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:5109733..5109798 26863196 MeRIP-seq:(Medium) rs770758794 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 112642 RMVar_ID_112642 Human_SNP_ID_829124540 m1A Human chr17 - 18971025 18971025 18971025 CGTAGGCTGCCTCCAGCTGCCCGTAACCACCGATCTGGTCAAAAGCTGGAGGGGTCAGGGTGGAA CGTAGGCTGCCTCCAGCTGCCCGTAACCACCGGTCTGGTCAAAAGCTGGAGGGGTCAGGGTGGAA T C FAM83G Ensembl:ENSG00000188522 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18970976..18971480 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 8 kidney Human_RBP_ID_27449469 112643 RMVar_ID_112643 Human_SNP_ID_829127657 m1A Human chr17 - 29575875 29575875 29575875 GGGTTTCAGATCCGGAAAGGGGTGTCTGCCTCAGCTGTGCCCTTCACTCCCTCCTCCCCGCTGCT GGGTTTCAGATCCGGAAAGGGGTGTCTGCCTCTGCTGTGCCCTTCACTCCCTCCTCCCCGCTGCT T A GIT1 Ensembl:ENSG00000108262 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:29575809..29575880 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung Human_RBP_ID_486352,Human_RBP_ID_764572,Human_RBP_ID_899726,Human_RBP_ID_9288937,Human_RBP_ID_18693244,Human_RBP_ID_27450713 Human_Splice_Rec_1798918,Human_Splice_Rec_1798919,Human_Splice_Rec_1798942,Human_Splice_Rec_1798943,Human_Splice_Rec_1798980,Human_Splice_Rec_1798981,Human_Splice_Rec_1799021,Human_Splice_Rec_1799058,Human_Splice_Rec_1799059,Human_Splice_Rec_1799076,Human_Splice_Rec_1799077,Human_Splice_Rec_1799086 Human_miRNA_ID_826784 RMVar_hsa_circ_24174,RMVar_hsa_circ_87716,RMVar_hsa_circ_373203,RMVar_hsa_circ_183144,RMVar_hsa_circ_87223,RMVar_hsa_circ_183147,RMVar_hsa_circ_183148,RMVar_hsa_circ_183149,RMVar_hsa_circ_377750 112644 RMVar_ID_112644 Human_SNP_ID_829128394 m1A Human chr17 - 40219368 40219368 40219368 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCTTTTGCCAACCCGGAAATGGATCTG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCTTTTGCCAACCCGGAAATGGATCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:40219303..40220419;chr17:40219324..40260629;chr17:40219301..40260655;chr17:40219301..40220419;chr17:40219308..40219561 26863196 MeRIP-seq:(Medium) rs879141289 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 10 pancreas 112645 RMVar_ID_112645 Human_SNP_ID_829132059 m1A Human chr17 - 74768518 74768518 74768518 TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTAGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG TTGAAGTCTAGGATGGGGTCGGAGGAGGAGGTTGACGAGGGCGCTGTGGAGTCCTGTTTTGGGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr17:74768448..74768702;chr17:74768451..74768600;chr17:74768451..74768550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 112646 RMVar_ID_112646 Human_SNP_ID_829135601 m1A Human chr17 + 19508237 19508237 19508237 GTCTGACTCCAGATCAGAAGGTTGCGTGTTCAAGTCACGTCGGGGTCAAGGTTGGGTTTTTTTTT GTCTGACTCCAGATCAGAAGGTTGCGTGTTCAGGTCACGTCGGGGTCAAGGTTGGGTTTTTTTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 PEME 1 - 112647 RMVar_ID_112647 Human_SNP_ID_829136154 m1A Human chr17 - 82064926 82064926 82064926 GCTGAGCCGGCGCCACGGGGCACAGCTCTGCTACACGCCCATGCTGCATGCCCAGGTCTTTGTCC GCTGAGCCGGCGCCACGGGGCACAGCTCTGCTGCACGCCCATGCTGCATGCCCAGGTCTTTGTCC T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82064876..82065111 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_503408,Human_RBP_ID_1545467,Human_RBP_ID_4461028,Human_RBP_ID_8825088 Human_miRNA_ID_42167,Human_miRNA_ID_70885,Human_miRNA_ID_1938352,Human_miRNA_ID_1949452 RMVar_hsa_circ_7198,RMVar_hsa_circ_126795,RMVar_hsa_circ_187846 112648 RMVar_ID_112648 Human_SNP_ID_829138333 m1A Human chr17 + 7327726 7327726 7327726 CGGTCCCCTTCACCAAGCTGGTCCAGGTCCTGACCATACTCCTCCAACACAGAGCGTCCATCTCT CGGTCCCCTTCACCAAGCTGGTCCAGGTCCTGGCCATACTCCTCCAACACAGAGCGTCCATCTCT A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7327677..7327760 26863196 MeRIP-seq:(Medium) rs1414017722 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 112649 RMVar_ID_112649 Human_SNP_ID_829145290 m1A Human chr17 - 81557764 81557764 81557764 CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTATTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT CCAGTTGGGTTGGGTCTGGTCACGGCAGAGCTTTTGTGGAGGGTCAGGAAGGGTGGAGAGGAGCT T A NPLOC4 Ensembl:ENSG00000182446 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81557716..81557783 26863196 MeRIP-seq:(Medium) rs8068511 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5319363,Human_RBP_ID_6651229,Human_RBP_ID_18459997,Human_RBP_ID_26456352 GWAS_ID_13195,GWAS_ID_13196,GWAS_ID_13197,GWAS_ID_13198 RMVar_hsa_circ_111199,RMVar_hsa_circ_114254,RMVar_hsa_circ_378526,RMVar_hsa_circ_377932,RMVar_hsa_circ_112503,RMVar_hsa_circ_187650,RMVar_hsa_circ_187654,RMVar_hsa_circ_97157,RMVar_hsa_circ_109785,RMVar_hsa_circ_187655,RMVar_hsa_circ_187656,RMVar_hsa_circ_187652,RMVar_hsa_circ_187653,RMVar_hsa_circ_187651 112650 RMVar_ID_112650 Human_SNP_ID_829145609 m1A Human chr17 - 76688172 76688172 76688172 GGGCACTGACCCTGTCCTTGTCTTGCAGGAAGAGGAGCAGGACTTGGATGGTGAGAAGGGGCCAT GGGCACTGACCCTGTCCTTGTCTTGCAGGAAGCGGAGCAGGACTTGGATGGTGAGAAGGGGCCAT T G MXRA7 Ensembl:ENSG00000182534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76688084..76688210 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_238243 Human_Splice_Rec_1872228,Human_Splice_Rec_1872229,Human_Splice_Rec_1872234,Human_Splice_Rec_1872235,Human_Splice_Rec_1872242,Human_Splice_Rec_1872243,Human_Splice_Rec_1872247,Human_Splice_Rec_1872252,Human_Splice_Rec_1872253,Human_Splice_Rec_1872258,Human_Splice_Rec_1872259,Human_Splice_Rec_1872264,Human_Splice_Rec_1872265 112651 RMVar_ID_112651 Human_SNP_ID_829155315 m1A Human chr17 + 82433808 82433808 82433808 TGGAGCTACACCCAGGCGCCCAGCGGCTGCACATCGGGTGTGATGAGGTGGGTACTGTCACCCCA TGGAGCTACACCCAGGCGCCCAGCGGCTGCACGTCGGGTGTGATGAGGTGGGTACTGTCACCCCA A G HEXD Ensembl:ENSG00000169660 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4789773 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 13 large intestine,breast Human_RBP_ID_3951511,Human_RBP_ID_18993131 Human_Splice_Rec_1885327,Human_Splice_Rec_1885349,Human_Splice_Rec_1885369,Human_Splice_Rec_1885391,Human_Splice_Rec_1885403,Human_Splice_Rec_1885427,Human_Splice_Rec_1885441,Human_Splice_Rec_1885465,Human_Splice_Rec_1885473,Human_Splice_Rec_1885493 GWAS_ID_13229,GWAS_ID_13230,GWAS_ID_13231,GWAS_ID_13232,GWAS_ID_13233,GWAS_ID_13234,GWAS_ID_13235,GWAS_ID_13236 RMVar_hsa_circ_96035,RMVar_hsa_circ_187940,RMVar_hsa_circ_98486,RMVar_hsa_circ_356158,RMVar_hsa_circ_187943 112652 RMVar_ID_112652 Human_SNP_ID_829164115 m1A Human chr17 + 78191058 78191058 78191058 AGCCTTGAGGACCTACTCACAGATAGGAATTGAAGGTACTAGTGTGACCTCTCCGTGGCCGCATT AGCCTTGAGGACCTACTCACAGATAGGAATTGGAGGTACTAGTGTGACCTCTCCGTGGCCGCATT A G AFMID Ensembl:ENSG00000183077 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78190951..78191097 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 12 lung Human_RBP_ID_900918,Human_RBP_ID_3953074,Human_RBP_ID_5362155,Human_RBP_ID_9376955,Human_RBP_ID_17653962,Human_RBP_ID_18989383,Human_RBP_ID_19080229,Human_RBP_ID_26332463,Human_RBP_ID_27813164 Human_Splice_Rec_1874736,Human_Splice_Rec_1874737,Human_Splice_Rec_1874756,Human_Splice_Rec_1874757,Human_Splice_Rec_1874766,Human_Splice_Rec_1874767,Human_Splice_Rec_1874770,Human_Splice_Rec_1874771,Human_Splice_Rec_1874776,Human_Splice_Rec_1874777,Human_Splice_Rec_1874788,Human_Splice_Rec_1874789,Human_Splice_Rec_1874800,Human_Splice_Rec_1874801,Human_Splice_Rec_1874808,Human_Splice_Rec_1874809,Human_Splice_Rec_1874812,Human_Splice_Rec_1874813,Human_Splice_Rec_1874832,Human_Splice_Rec_1874833,Human_Splice_Rec_1874840,Human_Splice_Rec_1874841,Human_Splice_Rec_1874843 RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_291188,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325,RMVar_hsa_circ_187323 112653 RMVar_ID_112653 Human_SNP_ID_829166362 m1A Human chr17 - 81801634 81801634 81801634 TGCCCGCAGCAAGATTCCTGTTATCTGGGTAGAGTCCTCAGCCTCCGCCACCCCCAGGCGATGTC TGCCCGCAGCAAGATTCCTGTTATCTGGGTAGGGTCCTCAGCCTCCGCCACCCCCAGGCGATGTC T C lnc-MCRIP1-1,lnc-MCRIP1-1:2 RNACentral:URS00008C3D98,RNACentral:URS00008C1A11 lincRNA,lincRNA intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81801626..81801711 26863196 MeRIP-seq:(Medium) rs1248322651 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112654 RMVar_ID_112654 Human_SNP_ID_829169436 m1A Human chr17 + 4716546 4716546 4716546 TCCCCCCGGTGCCCAACCCACCCCGGCCCCCCACCCGCCTGCAGGACCGGCTGCTGAGGAAGCTG TCCCCCCGGTGCCCAACCCACCCCGGCCCCCCCCCCGCCTGCAGGACCGGCTGCTGAGGAAGCTG A C ARRB2 Ensembl:ENSG00000141480 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:4716398..4716603 26863196 MeRIP-seq:(Medium) rs747331573 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,lung adenocarcinoma 10 lung Human_RBP_ID_492296,Human_RBP_ID_4474815 Human_Splice_Rec_1763973,Human_Splice_Rec_1764007,Human_Splice_Rec_1764021,Human_Splice_Rec_1764047,Human_Splice_Rec_1764071,Human_Splice_Rec_1764103,Human_Splice_Rec_1764135,Human_Splice_Rec_1764187,Human_Splice_Rec_1764207,Human_Splice_Rec_1764233,Human_Splice_Rec_1764251 112655 RMVar_ID_112655 Human_SNP_ID_829173830 m1A Human chr17 + 16353358 16353358 16353358 GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGAGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT GGTGGCGCTGGGTGCCAAGGCAGCGGCCGCGGGGGCCGCGGGGGCCGCGGAGGCCCCGGACCGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr17:16353080..16353450;chr17:16353076..16353450 26863410 MeRIP-seq:(Medium) rs754483275 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,ovary mixed_adenosquamous_carcinoma,LICA 3 ovary,head and neck 112656 RMVar_ID_112656 Human_SNP_ID_829174479 m1A Human chr17 + 47656983 47656982 47656983 AGTGGCCAGAACTCATTCCTCAGCTGGTGGCCAATGTCACAAACCCCAACAGCACAGAGCACATG AGTGGCCAGAACTCATTCCTCAGCTGGTGGCC_ATGTCACAAACCCCAACAGCACAGAGCACATG CA C KPNB1 Ensembl:ENSG00000108424 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47656933..47657079 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 GBM 1 - Human_RBP_ID_47232,Human_RBP_ID_201596,Human_RBP_ID_491887,Human_RBP_ID_1008672,Human_RBP_ID_1535706,Human_RBP_ID_1860904,Human_RBP_ID_3526424,Human_RBP_ID_3952600,Human_RBP_ID_6605491,Human_RBP_ID_8455074,Human_RBP_ID_8818912,Human_RBP_ID_9257879,Human_RBP_ID_9287667,Human_RBP_ID_17260220,Human_RBP_ID_17376054,Human_RBP_ID_17491795,Human_RBP_ID_17894378,Human_RBP_ID_18439170,Human_RBP_ID_18700546,Human_RBP_ID_22443023 Human_Splice_Rec_1832559,Human_Splice_Rec_1832609,Human_Splice_Rec_1832651,Human_Splice_Rec_1832661,Human_Splice_Rec_1832667,Human_Splice_Rec_1832703 Human_miRNA_ID_2675886,Human_miRNA_ID_2926637,Human_miRNA_ID_3067429 RMVar_hsa_circ_14,RMVar_hsa_circ_103109,RMVar_hsa_circ_105187,RMVar_hsa_circ_44107,RMVar_hsa_circ_81118,RMVar_hsa_circ_184985,RMVar_hsa_circ_184986,RMVar_hsa_circ_124020,RMVar_hsa_circ_184987,RMVar_hsa_circ_323619,RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_184988,RMVar_hsa_circ_375221,RMVar_hsa_circ_353897,RMVar_hsa_circ_75680,RMVar_hsa_circ_125661,RMVar_hsa_circ_62822,RMVar_hsa_circ_110452,RMVar_hsa_circ_184990,RMVar_hsa_circ_184992,RMVar_hsa_circ_184994,RMVar_hsa_circ_42980,RMVar_hsa_circ_184993,RMVar_hsa_circ_184991,RMVar_hsa_circ_294641,RMVar_hsa_circ_376640,RMVar_hsa_circ_184989,RMVar_hsa_circ_334978,RMVar_hsa_circ_270161,RMVar_hsa_circ_24523,RMVar_hsa_circ_76937,RMVar_hsa_circ_3055,RMVar_hsa_circ_184996,RMVar_hsa_circ_184998,RMVar_hsa_circ_184999,RMVar_hsa_circ_185000,RMVar_hsa_circ_184997,RMVar_hsa_circ_184995 112657 RMVar_ID_112657 Human_SNP_ID_829175179 m1A Human chr17 + 50482198 50482198 50482198 GCCCGGCGCCTCTTTCCCGGGCGCGTGTCTGTAGACTTGATGCTGGGGCTGCCGGCACAGCAGGT GCCCGGCGCCTCTTTCCCGGGCGCGTGTCTGTGGACTTGATGCTGGGGCTGCCGGCACAGCAGGT A G RSAD1 Ensembl:ENSG00000136444 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7210579 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,mouth squamous_cell_carcinoma,liver neoplasm,large_intestine adenocarcinoma 4 liver,head and neck,large intestine Human_RBP_ID_5367435,Human_RBP_ID_22588346 RMVar_hsa_circ_100390,RMVar_hsa_circ_91057,RMVar_hsa_circ_185337,RMVar_hsa_circ_185338 112658 RMVar_ID_112658 Human_SNP_ID_829184456 m1A Human chr17 + 80840852 80840852 80840852 CCGCAGCTCACACTCACCGCACGGCAGCTCACACTCACCACACGGCAGCTCACTCTCACCACACG CCGCAGCTCACACTCACCGCACGGCAGCTCACTCTCACCACACGGCAGCTCACTCTCACCACACG A T RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:80840718..80840875 26863196 MeRIP-seq:(Medium) rs1431176632 Functional Loss SNV ICGC 33..33 33 PBCA 4 - RMVar_hsa_circ_59,RMVar_hsa_circ_127509,RMVar_hsa_circ_77466,RMVar_hsa_circ_187523,RMVar_hsa_circ_187524,RMVar_hsa_circ_7919,RMVar_hsa_circ_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_19144,RMVar_hsa_circ_10994,RMVar_hsa_circ_344276,RMVar_hsa_circ_33259,RMVar_hsa_circ_7214,RMVar_hsa_circ_187538,RMVar_hsa_circ_86459,RMVar_hsa_circ_292318,RMVar_hsa_circ_373270,RMVar_hsa_circ_115638,RMVar_hsa_circ_187539,RMVar_hsa_circ_187540 112659 RMVar_ID_112659 Human_SNP_ID_829184726 m1A Human chr17 + 80111415 80111415 80111415 TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCAGGAATTACCAAGAAGAAGCATGGGGGTCAGGG TTCTAGCCAGGGAGCAGGGTGGGCTCAGAGGCGGGAATTACCAAGAAGAAGCATGGGGGTCAGGG A G GAA Ensembl:ENSG00000171298 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7209921 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_2524965,Human_RBP_ID_5365190,Human_RBP_ID_8232684,Human_RBP_ID_21974661,Human_RBP_ID_22500646 RMVar_hsa_circ_64421 112660 RMVar_ID_112660 Human_SNP_ID_829187802 m1A Human chr17 + 17795407 17795407 17795407 CTTCAAGCAGGAGGAGGTGGGTGGGGTGAAGGAGGAGGCAGGTGGGCTGCTGCAGTGCCCCGAGG CTTCAAGCAGGAGGAGGTGGGTGGGGTGAAGGTGGAGGCAGGTGGGCTGCTGCAGTGCCCCGAGG A T RAI1 Ensembl:ENSG00000108557 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:17795268..17795585 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_899495,Human_RBP_ID_5525391,Human_RBP_ID_22443477,Human_RBP_ID_22716452,Human_RBP_ID_27449069 RMVar_hsa_circ_336571,RMVar_hsa_circ_347695,RMVar_hsa_circ_182407 112661 RMVar_ID_112661 Human_SNP_ID_829195728 m1A Human chr17 + 8146931 8146931 8146931 GGGAGGCGGGGCCGGGACTGAGGCCGGGCCCGAGACTCAATAAAAAGCTGCTGGCCCTGGTGCTT GGGAGGCGGGGCCGGGACTGAGGCCGGGCCCGGGACTCAATAAAAAGCTGCTGGCCCTGGTGCTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:8146732..8146985 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 112662 RMVar_ID_112662 Human_SNP_ID_829197964 m1A Human chr17 + 36545659 36545638 36545659 TGGGAGGAGGCGGCAGCGGCGGCGGCAGAAACAGCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAG TGGGAGGAGGCG_____________________GCAGCGGCGGCGGCGGCGGCAGCTGGGAGGAG GGCAGCGGCGGCGGCAGAAACA G GGNBP2 Ensembl:ENSG00000278311 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:36544951..36545825 26863196 MeRIP-seq:(Medium) rs1366786146 Functional Loss DEL ICGC 13..33 33 LICA 1 - Human_RBP_ID_8825439,Human_RBP_ID_9288977,Human_RBP_ID_18419578 Human_Splice_Rec_1807224,Human_Splice_Rec_1807226,Human_Splice_Rec_1807240,Human_Splice_Rec_1807266 RMVar_hsa_circ_65606,RMVar_hsa_circ_183718 112663 RMVar_ID_112663 Human_SNP_ID_829209800 m1A Human chr17 - 21012881 21012881 21012881 CAACAACCCCAACCACTGCAACTGCATCATAGACCAGATCTTCACAGGCGGGTTGCAGTCAGACG CAACAACCCCAACCACTGCAACTGCATCATAGTCCAGATCTTCACAGGCGGGTTGCAGTCAGACG T A USP22 Ensembl:ENSG00000124422 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:21012826..21012900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_RBP_ID_1529411,Human_RBP_ID_1851000,Human_RBP_ID_3515117,Human_RBP_ID_3950199,Human_RBP_ID_6569220,Human_RBP_ID_8814260,Human_RBP_ID_9286904,Human_RBP_ID_17258418,Human_RBP_ID_17887037,Human_RBP_ID_18289697,Human_RBP_ID_18530504,Human_RBP_ID_18691501,Human_RBP_ID_26956725 Human_Splice_Rec_1793096,Human_Splice_Rec_1793097,Human_Splice_Rec_1793120,Human_Splice_Rec_1793121,Human_Splice_Rec_1793148,Human_Splice_Rec_1793149,Human_Splice_Rec_1793176 Human_miRNA_ID_2473404 RMVar_hsa_circ_2515,RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_81808,RMVar_hsa_circ_182718,RMVar_hsa_circ_182722,RMVar_hsa_circ_317048,RMVar_hsa_circ_374685,RMVar_hsa_circ_310247,RMVar_hsa_circ_125521,RMVar_hsa_circ_51758,RMVar_hsa_circ_182724,RMVar_hsa_circ_182725,RMVar_hsa_circ_182723,RMVar_hsa_circ_301801,RMVar_hsa_circ_378132,RMVar_hsa_circ_324166,RMVar_hsa_circ_103075,RMVar_hsa_circ_182734,RMVar_hsa_circ_182735,RMVar_hsa_circ_14248,RMVar_hsa_circ_182737,RMVar_hsa_circ_97245,RMVar_hsa_circ_275750,RMVar_hsa_circ_114722,RMVar_hsa_circ_182738,RMVar_hsa_circ_182739,RMVar_hsa_circ_182740,RMVar_hsa_circ_268517,RMVar_hsa_circ_337341,RMVar_hsa_circ_369578,RMVar_hsa_circ_182741 112664 RMVar_ID_112664 Human_SNP_ID_829210393 m1A Human chr17 - 42577680 42577680 42577680 TTCTGAGTTGGGTGGCGGGAAAGGCGATGAGTAAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAAC TTCTGAGTTGGGTGGCGGGAAAGGCGATGAGTGAAGGCCGGGCAGAAGCTGCGGCGGGAGGTAAC T C PSMC3IP Ensembl:ENSG00000131470 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:42577568..42577697 26863196 MeRIP-seq:(Medium) rs373107959 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_489823,Human_RBP_ID_4428311,Human_RBP_ID_18419958,Human_RBP_ID_18988513,Human_RBP_ID_23726876,Human_RBP_ID_27812711,Human_RBP_ID_27838451 Human_Splice_Rec_1819883,Human_Splice_Rec_1819897,Human_Splice_Rec_1819923,Human_Splice_Rec_1819951,Human_Splice_Rec_1819963,Human_Splice_Rec_1819977 RMVar_hsa_circ_98110,RMVar_hsa_circ_184413 112665 RMVar_ID_112665 Human_SNP_ID_829222186 m1A Human chr17 + 78973170 78973170 78973170 TCGCAGCCCCGCTGGCTGTCAAAGATCTGGCCAAGGGCCTCCGAGAGCTCCCTGGAGAGGTCCAG TCGCAGCCCCGCTGGCTGTCAAAGATCTGGCCGAGGGCCTCCGAGAGCTCCCTGGAGAGGTCCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:78972950..78973176 26863196 MeRIP-seq:(Medium) rs1269568943 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 112666 RMVar_ID_112666 Human_SNP_ID_829224907 m1A Human chr17 - 7854188 7854188 7854188 GGCCGGGCCCGGACACACACTGGGGCGCGGGGAGAGCCCGGCGACGGGCGGTCCCTGGAGGGGCG GGCCGGGCCCGGACACACACTGGGGCGCGGGGGGAGCCCGGCGACGGGCGGTCCCTGGAGGGGCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7854149..7854249 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112667 RMVar_ID_112667 Human_SNP_ID_829233419 m1A Human chr17 - 7893501 7893501 7893501 GGGGCTGGATATCAGCAGCAGGGGGTGGTGGAAGGGCGGGGGGTCCGGAGGGTGCTATGGGGGTG GGGGCTGGATATCAGCAGCAGGGGGTGGTGGAGGGGCGGGGGGTCCGGAGGGTGCTATGGGGGTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7893451..7893550 26863196 MeRIP-seq:(Medium) rs749149678 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 112668 RMVar_ID_112668 Human_SNP_ID_829239013 m1A Human chr17 + 81078446 81078446 81078446 TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTATGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG TGGGTGCAGGTGCCATCTCGGAGCTGGGTGCTGTGGGTGCGGGTGCCGTATTGGGTGGGAGCCGG A G BAIAP2 Ensembl:ENSG00000175866 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:81078056..81078721;chr17:81078107..81078682 26863196 MeRIP-seq:(Medium) rs368379695 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,CHOL 7 prostate RMVar_hsa_circ_12563,RMVar_hsa_circ_267105,RMVar_hsa_circ_290688,RMVar_hsa_circ_23177,RMVar_hsa_circ_187574,RMVar_hsa_circ_63293 112669 RMVar_ID_112669 Human_SNP_ID_829245027 m1A Human chr17 - 7258928 7258924 7258928 CTCAGGGATCCACGTACCCAGGTCCCAACCTTACTTTTCAGAACTGAACTGGAAGGGCAGGATCA CTCAGGGATCCACGTACCCAGGTCCCAACCTT____TTCAGAACTGAACTGGAAGGGCAGGATCA AAAGT A AC003688.2 Ensembl:ENSG00000262302 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7258901..7258950 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..36 33 READ 1 - 112670 RMVar_ID_112670 Human_SNP_ID_829246124 m1A Human chr17 - 80101627 80101627 80101627 CTCAGGGAAGCCCCGCAGCCCCGGCCCGGCTCACCTCCGCGCACGCGCGCCCTGGCCGCCCGCGG CTCAGGGAAGCCCCGCAGCCCCGGCCCGGCTCCCCTCCGCGCACGCGCGCCCTGGCCGCCCGCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr17:80101580..80101940;chr17:80101620..80101817 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary 112671 RMVar_ID_112671 Human_SNP_ID_829247522 m1A Human chr17 + 45099512 45099512 45099512 GCAGCGCACCATGAAGCTCTACCGACTGCCAGAGGCCAGTGCTGCCCCGGGTGGTGGGCAGGGGG GCAGCGCACCATGAAGCTCTACCGACTGCCAGCGGCCAGTGCTGCCCCGGGTGGTGGGCAGGGGG A C NMT1 Ensembl:ENSG00000136448 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:45099478..45099584 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_896635,Human_RBP_ID_3952559,Human_RBP_ID_5115179,Human_RBP_ID_8454222,Human_RBP_ID_19079336 RMVar_hsa_circ_100911,RMVar_hsa_circ_110318,RMVar_hsa_circ_184793,RMVar_hsa_circ_325254,RMVar_hsa_circ_184794 112672 RMVar_ID_112672 Human_SNP_ID_829254332 m1A Human chr17 - 7675149 7675137 7675149 AGCTGTGGGTTGATTCCACACCCCCGCCCGGCACCCGCGTCCGCGCCATGGCCATCTACAAGCAG AGCTGTGGGTTGATTCCACACCCCCGCCCGGC____________GCCATGGCCATCTACAAGCAG CGCGGACGCGGGT C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr17:7674965..7675200;chr17:7675103..7675203 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..44 33 GBM 1 - Human_RBP_ID_4454226,Human_RBP_ID_18987867,Human_RBP_ID_27812234 Human_Splice_Rec_1773744,Human_Splice_Rec_1773745,Human_Splice_Rec_1773758,Human_Splice_Rec_1773759,Human_Splice_Rec_1773778,Human_Splice_Rec_1773779,Human_Splice_Rec_1773789,Human_Splice_Rec_1773803,Human_Splice_Rec_1773817,Human_Splice_Rec_1773829,Human_Splice_Rec_1773841,Human_Splice_Rec_1773855,Human_Splice_Rec_1773874,Human_Splice_Rec_1773875,Human_Splice_Rec_1773894,Human_Splice_Rec_1773895,Human_Splice_Rec_1773914,Human_Splice_Rec_1773915,Human_Splice_Rec_1773934,Human_Splice_Rec_1773935,Human_Splice_Rec_1773956,Human_Splice_Rec_1773957,Human_Splice_Rec_1773978,Human_Splice_Rec_1773979,Human_Splice_Rec_1774000,Human_Splice_Rec_1774001,Human_Splice_Rec_1774022,Human_Splice_Rec_1774023,Human_Splice_Rec_1774044,Human_Splice_Rec_1774045,Human_Splice_Rec_1774064,Human_Splice_Rec_1774065,Human_Splice_Rec_1774083,Human_Splice_Rec_1774096,Human_Splice_Rec_1774097,Human_Splice_Rec_1774110,Human_Splice_Rec_1774111,Human_Splice_Rec_1774115,Human_Splice_Rec_1774122,Human_Splice_Rec_1774123,Human_Splice_Rec_1774132,Human_Splice_Rec_1774140,Human_Splice_Rec_1774150 Human_miRNA_ID_2975800 RMVar_hsa_circ_20059,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_323715,RMVar_hsa_circ_43650,RMVar_hsa_circ_181930 112673 RMVar_ID_112673 Human_SNP_ID_829258426 m1A Human chr17 + 6641096 6641094 6641097 GCGGCTGCACGTCGTGCCAATGGCCCGCTATGAGGAGGTGAGCGTGTCCGGCTTCGAGGAGTTCC GCGGCTGCACGTCGTGCCAATGGCCCGCTAT___GAGGTGAGCGTGTCCGGCTTCGAGGAGTTCC TGAG T TXNDC17 Ensembl:ENSG00000129235 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 32..34 33 STAD,UCEC 2 - Human_RBP_ID_497983,Human_RBP_ID_4446843,Human_RBP_ID_5318849,Human_RBP_ID_5467488,Human_RBP_ID_8941879,Human_RBP_ID_26969458 Human_Splice_Rec_1768191 112674 RMVar_ID_112674 Human_SNP_ID_829260550 m1A Human chr17 - 7676201 7676201 7676201 TCCCCGGACGATATTGAACAATGGTTCACTGAAGACCCAGGTCCAGATGAAGCTCCCAGAATGCC TCCCCGGACGATATTGAACAATGGTTCACTGAGGACCCAGGTCCAGATGAAGCTCCCAGAATGCC T C TP53 Ensembl:ENSG00000141510 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Normoxia chr17:7676151..7676225;chr17:7676150..7676250 26863196,32194978 MeRIP-seq:(Medium) rs574255227 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue peripheral_T_cell_lymphoma_unspecified,lymph_node peripheral_T_cell_lymphoma_unspecified 13 haematopoietic and lymphoid tissue Human_RBP_ID_501225,Human_RBP_ID_1869946,Human_RBP_ID_3538266,Human_RBP_ID_3951795,Human_RBP_ID_4454239,Human_RBP_ID_6647588,Human_RBP_ID_13178643 Human_Splice_Rec_1773742,Human_Splice_Rec_1773756,Human_Splice_Rec_1773776,Human_Splice_Rec_1773872,Human_Splice_Rec_1773892,Human_Splice_Rec_1773912,Human_Splice_Rec_1773932,Human_Splice_Rec_1773954,Human_Splice_Rec_1773976,Human_Splice_Rec_1773998,Human_Splice_Rec_1774020,Human_Splice_Rec_1774042,Human_Splice_Rec_1774062,Human_Splice_Rec_1774082,Human_Splice_Rec_1774120,Human_Splice_Rec_1774130,Human_Splice_Rec_1774138,Human_Splice_Rec_1774148 Clinvar_Rec_662 RMVar_hsa_circ_20059,RMVar_hsa_circ_43650 112675 RMVar_ID_112675 Human_SNP_ID_829262783 m1A Human chr17 - 39672243 39672243 39672243 TGCTGGGATTGGGAAGGAGTTTCACCCTGACCATTGCCCTAGCCAGGTTCCCAGGAGGCCTCACC TGCTGGGATTGGGAAGGAGTTTCACCCTGACCGTTGCCCTAGCCAGGTTCCCAGGAGGCCTCACC T C PGAP3 Ensembl:ENSG00000161395 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2952151 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_15215,GWAS_ID_15216,GWAS_ID_15217,GWAS_ID_15218,GWAS_ID_15219,GWAS_ID_15220,GWAS_ID_15221 112676 RMVar_ID_112676 Human_SNP_ID_829265560 m1A Human chr17 + 16439562 16439562 16439562 AGTGCCGTCAGAAGCGATAACTGACGACGTCTAATGTCTATCTGACCGCAGTCGCTGAAACCTCT AGTGCCGTCAGAAGCGATAACTGACGACGTCTCATGTCTATCTGACCGCAGTCGCTGAAACCTCT A C SNORD49B,SNHG29 Ensembl:ENSG00000277108,Ensembl:ENSG00000175061 snoRNA,lincRNA exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:16439558..16439651 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_237291,Human_RBP_ID_269807,Human_RBP_ID_483842,Human_RBP_ID_768564,Human_RBP_ID_1006418,Human_RBP_ID_1091556,Human_RBP_ID_1284571,Human_RBP_ID_1528461,Human_RBP_ID_1849822,Human_RBP_ID_2495150,Human_RBP_ID_3513482,Human_RBP_ID_5184391,Human_RBP_ID_6563363,Human_RBP_ID_8253189,Human_RBP_ID_8445108,Human_RBP_ID_8813550,Human_RBP_ID_9069420,Human_RBP_ID_12902209,Human_RBP_ID_17258135,Human_RBP_ID_18207736,Human_RBP_ID_18689950,Human_RBP_ID_20291422,Human_RBP_ID_22655885,Human_RBP_ID_22740218,Human_RBP_ID_22947334,Human_RBP_ID_23712918,Human_RBP_ID_25252787,Human_RBP_ID_26955167,Human_RBP_ID_27250025 Human_Splice_Rec_1784006,Human_Splice_Rec_1784092,Human_Splice_Rec_1784150,Human_Splice_Rec_1784166,Human_Splice_Rec_1784210,Human_Splice_Rec_1784300,Human_Splice_Rec_1784314,Human_Splice_Rec_1784328,Human_Splice_Rec_1784340,Human_Splice_Rec_1784358 RMVar_hsa_circ_4506,RMVar_hsa_circ_5195,RMVar_hsa_circ_182331,RMVar_hsa_circ_117464 112677 RMVar_ID_112677 Human_SNP_ID_829269480 m1A Human chr17 - 13005417 13005417 13005417 GGCCTGGGGTTTATGGTCCAGAGGAATGCCACAGTATTCTATGTCAAGATATTTCCTCTGACTTC GGCCTGGGGTTTATGGTCCAGAGGAATGCCACTGTATTCTATGTCAAGATATTTCCTCTGACTTC T A ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4792310 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 3 liver Human_RBP_ID_21975404 GWAS_ID_13696 RMVar_hsa_circ_76884,RMVar_hsa_circ_182179,RMVar_hsa_circ_99844,RMVar_hsa_circ_63049,RMVar_hsa_circ_110157,RMVar_hsa_circ_182180,RMVar_hsa_circ_372822,RMVar_hsa_circ_182181,RMVar_hsa_circ_23609,RMVar_hsa_circ_182183 112678 RMVar_ID_112678 Human_SNP_ID_829271041 m1A Human chr17 - 62666869 62666869 62666869 GCTGCCCTGCGCCCCCAACCTTGTGCCTCACCACTCTCCCAGTTGAGGTACTTGAGGGGCGAGTT GCTGCCCTGCGCCCCCAACCTTGTGCCTCACCGCTCTCCCAGTTGAGGTACTTGAGGGGCGAGTT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:62666826..62666875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - 112679 RMVar_ID_112679 Human_SNP_ID_829281359 m1A Human chr17 - 4897307 4897307 4897307 CTGCAGGGGGAGAGCTGGGTCCAGTGTGGGACAGCCCCAGCCCAGGGCCCCGTCACCAGTTCATG CTGCAGGGGGAGAGCTGGGTCCAGTGTGGGACCGCCCCAGCCCAGGGCCCCGTCACCAGTTCATG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:4897214..4897414 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 112680 RMVar_ID_112680 Human_SNP_ID_829285873 m1A Human chr17 - 82079358 82079358 82079358 CGAGGACCTGGGCGCGGACTACAACCTCTCCCAGGTGCGCAAGGGGCCTGACGGGAACGGGGACA CGAGGACCTGGGCGCGGACTACAACCTCTCCCGGGTGCGCAAGGGGCCTGACGGGAACGGGGACA T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:82079351..82079375 26863196 MeRIP-seq:(Medium) rs1325108382 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_19084695 Human_Splice_Rec_1884445,Human_Splice_Rec_1884529,Human_Splice_Rec_1884531,Human_Splice_Rec_1884537,Human_Splice_Rec_1884545,Human_Splice_Rec_1884547 RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_112803,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187858,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848 112681 RMVar_ID_112681 Human_SNP_ID_829287365 m1A Human chr17 + 14207230 14207230 14207230 GCCCCCTCCCAGCTGAGAGCACTGGGACGCCCACCGCCCCTTTCCCTCCGCTGCCAGGCGAGCAT GCCCCCTCCCAGCTGAGAGCACTGGGACGCCCGCCGCCCCTTTCCCTCCGCTGCCAGGCGAGCAT A G COX10 Ensembl:ENSG00000006695 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:14207090..14207240 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_1781675 Human_miRNA_ID_2387208,Human_miRNA_ID_2388681,Human_miRNA_ID_2399830,Human_miRNA_ID_2873934,Human_miRNA_ID_2981896,Human_miRNA_ID_3030887 RMVar_hsa_circ_182201,RMVar_hsa_circ_79288,RMVar_hsa_circ_182202 112682 RMVar_ID_112682 Human_SNP_ID_829288120 m1A Human chr17 + 7307685 7307679 7307685 GCGGCGGCGGTAGAGGCGGCGGCGGCGGCGGCAGCGGGCTCGGAGGCAGCGGTTGGGCTCGCGGC GCGGCGGCGGTAGAGGCGGCGGCGGCG______GCGGGCTCGGAGGCAGCGGTTGGGCTCGCGGC GGCGGCA G EIF5A Ensembl:ENSG00000132507 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr17:7307493..7308145;chr17:7307551..7308075;chr17:7307551..7307851;chr17:7307501..7308150;chr17:7307501..7308408 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 28..33 33 ESCA 1 - Human_RBP_ID_237834,Human_RBP_ID_768533,Human_RBP_ID_4464301,Human_RBP_ID_5318228,Human_RBP_ID_5526160,Human_RBP_ID_6641900,Human_RBP_ID_8941803,Human_RBP_ID_9326449,Human_RBP_ID_13154951,Human_RBP_ID_22442772 Human_Splice_Rec_1771041,Human_Splice_Rec_1771053,Human_Splice_Rec_1771061,Human_Splice_Rec_1771071,Human_Splice_Rec_1771081 112683 RMVar_ID_112683 Human_SNP_ID_829288644 m1A Human chr17 + 7937251 7937247 7937251 AGCAGGAAAGTGCCAGACTGCAGCAACGGGAAAGAGAGACACTGGTGAGAAGATTGGACTGGGTT AGCAGGAAAGTGCCAGACTGCAGCAACGG____GAGAGACACTGGTGAGAAGATTGGACTGGGTT GGAAA G CNTROB Ensembl:ENSG00000170037 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7937151..7937310 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 ESCA 1 - Human_RBP_ID_3950097,Human_RBP_ID_13188396,Human_RBP_ID_18990451,Human_RBP_ID_27812256 Human_Splice_Rec_1775478,Human_Splice_Rec_1775479,Human_Splice_Rec_1775514,Human_Splice_Rec_1775515,Human_Splice_Rec_1775556,Human_Splice_Rec_1775568,Human_Splice_Rec_1775569,Human_Splice_Rec_1775604,Human_Splice_Rec_1775605,Human_Splice_Rec_1775614,Human_Splice_Rec_1775615,Human_Splice_Rec_1775635,Human_Splice_Rec_1775647 RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_347345,RMVar_hsa_circ_63051,RMVar_hsa_circ_323910,RMVar_hsa_circ_332345,RMVar_hsa_circ_19764 112684 RMVar_ID_112684 Human_SNP_ID_829294063 m1A Human chr17 - 51120451 51120451 51120451 GGAGAACCTGGACTCGGTGTTCGCGCAGGACCAGGAGCACCAGGTGGAGCTGGAGCTGCTGCGGG GGAGAACCTGGACTCGGTGTTCGCGCAGGACCGGGAGCACCAGGTGGAGCTGGAGCTGCTGCGGG T C SPAG9 Ensembl:ENSG00000008294 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr17:51120400..51120818;chr17:51120351..51120815 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_237454,Human_RBP_ID_767886,Human_RBP_ID_9290216,Human_RBP_ID_9378568,Human_RBP_ID_13071581,Human_RBP_ID_17895932,Human_RBP_ID_18412061,Human_RBP_ID_18702428,Human_RBP_ID_25300622,Human_RBP_ID_26332091,Human_RBP_ID_27812913 Human_Splice_Rec_1841819,Human_Splice_Rec_1841871,Human_Splice_Rec_1841979,Human_Splice_Rec_1842035 RMVar_hsa_circ_266744 112685 RMVar_ID_112685 Human_SNP_ID_829295838 m1A Human chr17 - 7014164 7014164 7014164 ACAGTTGTAGCTGACTTGCTCGTAAAGGTTGTATATGTTCTGGGGGCCATTCCTGGGGGTGGGAA ACAGTTGTAGCTGACTTGCTCGTAAAGGTTGTCTATGTTCTGGGGGCCATTCCTGGGGGTGGGAA T G AC040977.2 Ensembl:ENSG00000267047 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:7014126..7014475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_6640895 112686 RMVar_ID_112686 Human_SNP_ID_829295870 m1A Human chr17 + 63550729 63550729 63550729 GGAAGGAGATCTACAAGTATGAAGCGCCCTGGACAGTCTACGCGATGAACTGGAGTGTGCGGCCC GGAAGGAGATCTACAAGTATGAAGCGCCCTGGCCAGTCTACGCGATGAACTGGAGTGTGCGGCCC A C DCAF7 Ensembl:ENSG00000136485 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:63550551..63550825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_237855,Human_RBP_ID_496805,Human_RBP_ID_1539753,Human_RBP_ID_1866540,Human_RBP_ID_4465604,Human_RBP_ID_6631765,Human_RBP_ID_9376526,Human_RBP_ID_13125576,Human_RBP_ID_18705612,Human_RBP_ID_23742601 Human_Splice_Rec_1851985,Human_Splice_Rec_1851997,Human_Splice_Rec_1852011,Human_Splice_Rec_1852015,Human_Splice_Rec_1852017 Human_miRNA_ID_311889 112687 RMVar_ID_112687 Human_SNP_ID_829303420 m1A Human chr17 - 3818496 3818493 3818496 GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGAAGACCAGGACATGGATGCAGATGACAGAGTGGT GAGGAGGAGGAGGAAGAGGAAGAGGAAGAAGA___CCAGGACATGGATGCAGATGACAGAGTGGT GTCT G NCBP3 Ensembl:ENSG00000074356 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:3818409..3818589 26863196 MeRIP-seq:(Medium) rs746673147 Functional Loss DEL TCGA 33..35 33 STAD 1 - Human_RBP_ID_235714,Human_RBP_ID_819421,Human_RBP_ID_899112,Human_RBP_ID_1181650,Human_RBP_ID_1546625,Human_RBP_ID_4423300,Human_RBP_ID_6590677,Human_RBP_ID_8232118,Human_RBP_ID_9375117,Human_RBP_ID_18990031,Human_RBP_ID_22950761,Human_RBP_ID_23118732,Human_RBP_ID_24544758,Human_RBP_ID_25341592,Human_RBP_ID_26331052,Human_RBP_ID_27812168 Human_Splice_Rec_1762044,Human_Splice_Rec_1762060,Human_Splice_Rec_1762078,Human_Splice_Rec_1762090 RMVar_hsa_circ_78681,RMVar_hsa_circ_328692,RMVar_hsa_circ_338607,RMVar_hsa_circ_269867,RMVar_hsa_circ_361062,RMVar_hsa_circ_181334 112688 RMVar_ID_112688 Human_SNP_ID_829311110 m1A Human chr17 + 1651292 1651292 1651292 CCACTGGGGGTCAGCTTGTAGGCCGTCAGTGTACAGGAGCCTGGCGTGAAGCTGGGGGAGGAACG CCACTGGGGGTCAGCTTGTAGGCCGTCAGTGTGCAGGAGCCTGGCGTGAAGCTGGGGGAGGAACG A G NONHSAG020469.2 RNACentral:URS00008B5AC2 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:1651101..1651325 32194978 MeRIP-seq:(Medium) rs753884759 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 112689 RMVar_ID_112689 Human_SNP_ID_829312455 m1A Human chr17 + 79834904 79834904 79834904 TTCTTGTTCTTGACTATCTTCATCTTGCCCCCAATCCCGTTGCCCGTCACAGCCTCTTTGGGGGC TTCTTGTTCTTGACTATCTTCATCTTGCCCCCGATCCCGTTGCCCGTCACAGCCTCTTTGGGGGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:79834701..79834991 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 112690 RMVar_ID_112690 Human_SNP_ID_829319086 m1A Human chr17 - 17811592 17811592 17811592 GCCACACTGGAGAGGGGGCACAGGGGCGGGGGAGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG GCCACACTGGAGAGGGGGCACAGGGGCGGGGGGGGTTTCCTGTTCTGTGAAAGGCCGACTCCCTG T C SREBF1 Ensembl:ENSG00000072310 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:17811547..17811692 26863196 MeRIP-seq:(Medium) rs984197391 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112691 RMVar_ID_112691 Human_SNP_ID_829321451 m1A Human chr17 - 41689943 41689943 41689943 TTATGACTTTCCCAAAATCTCACTGAAGACCTACTTTCTTAAACGCCTTCACTAGTTTCTTTTTA TTATGACTTTCCCAAAATCTCACTGAAGACCTGCTTTCTTAAACGCCTTCACTAGTTTCTTTTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41689918..41689991 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRC 1 - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 112692 RMVar_ID_112692 Human_SNP_ID_829327791 m1A Human chr17 + 7579837 7579835 7579837 AAAAGCCCAGGGGACAGGGAATGACTGTCCTCACAAAAAATCAGCTACTTTGCTGCCATCCTTCA AAAAGCCCAGGGGACAGGGAATGACTGTCCT__CAAAAAATCAGCTACTTTGCTGCCATCCTTCA TCA T AC016876.3,CD68 Ensembl:ENSG00000264772,Ensembl:ENSG00000129226 lincRNA,Protein coding exon,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:7579704..7580101 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 STAD 1 - Human_RBP_ID_4467632,Human_RBP_ID_5582146 Human_Splice_Rec_1773112 Human_miRNA_ID_3147815,Human_miRNA_ID_3202115 112693 RMVar_ID_112693 Human_SNP_ID_829336033 m1A Human chr17 + 22204399 22204399 22204399 AAGTGGAGCCCAGTGACACCATCGAAAATGTGAAGGCCAAGATCCAAGATAAAGAAGGCATCCCC AAGTGGAGCCCAGTGACACCATCGAAAATGTGTAGGCCAAGATCCAAGATAAAGAAGGCATCCCC A T UBBP4 Ensembl:ENSG00000263563 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_miRNA_ID_1824714,Human_miRNA_ID_1845056,Human_miRNA_ID_1845525,Human_miRNA_ID_1846001 112694 RMVar_ID_112694 Human_SNP_ID_829336411 m1A Human chr17 + 48944739 48944739 48944739 CGCCAGCTCCCACCCCGCGGCGGTGCATCCCCACCCTGGGCCCGCGGGCCGCCCGGCTGCCGGGA CGCCAGCTCCCACCCCGCGGCGGTGCATCCCCCCCCTGGGCCCGCGGGCCGCCCGGCTGCCGGGA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:48944128..48944769 32194978 MeRIP-seq:(Medium) rs780254745 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 112695 RMVar_ID_112695 Human_SNP_ID_829338515 m1A Human chr17 - 29568832 29568832 29568832 GGGCCGAGGCCTTCCCAGGAGCGGGTCACCTTACCTCGCTGGGACCCAGGAGCCTCGCGAGGGCT GGGCCGAGGCCTTCCCAGGAGCGGGTCACCTTCCCTCGCTGGGACCCAGGAGCCTCGCGAGGGCT T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:29568730..29568850 26863410 MeRIP-seq:(Medium) rs752294319 Functional Loss SNV ICGC 33..33 33 BLCA 1 - 112696 RMVar_ID_112696 Human_SNP_ID_829343715 m1A Human chr17 - 64188417 64188417 64188417 ATTGTGTGAATAGCCCCCGTCTTCTTGGCTCCAGGGCTTTTGCCTGCACACAGCAGACACAACAG ATTGTGTGAATAGCCCCCGTCTTCTTGGCTCCGGGGCTTTTGCCTGCACACAGCAGACACAACAG T C TEX2 Ensembl:ENSG00000136478 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:64188394..64193599 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 4 stomach Human_RBP_ID_23256940 Human_Splice_Rec_1854648 RMVar_hsa_circ_186416,RMVar_hsa_circ_14720,RMVar_hsa_circ_56166,RMVar_hsa_circ_349882,RMVar_hsa_circ_271359,RMVar_hsa_circ_115131,RMVar_hsa_circ_186417,RMVar_hsa_circ_337026 112697 RMVar_ID_112697 Human_SNP_ID_829346415 m1A Human chr17 - 67959642 67959642 67959642 GGTGAAGGTGGAGGGGCTGGAGGGGCTGGAGGAGCTGGTGTCACTGGGGGGCAGGGTGCAGCTAC GGTGAAGGTGGAGGGGCTGGAGGGGCTGGAGGGGCTGGTGTCACTGGGGGGCAGGGTGCAGCTAC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:67959592..67959746 26863196 MeRIP-seq:(Medium) rs202116659 Functional Loss SNV ICGC,COSMIC 33..33 33 rectum adenocarcinoma,LICA,liver neoplasm,large_intestine adenocarcinoma 9 liver,large intestine 112698 RMVar_ID_112698 Human_SNP_ID_829353119 m1A Human chr17 - 82081805 82081805 82081805 CCGTGCAGTGGGGCGCCATCGGCGACGTGGGCATTTTGGTGGAGACGATGAGCACCAACGACACG CCGTGCAGTGGGGCGCCATCGGCGACGTGGGCGTTTTGGTGGAGACGATGAGCACCAACGACACG T C FASN Ensembl:ENSG00000169710 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:82081758..82081849 26863196 MeRIP-seq:(Medium) rs946823999 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_4481282,Human_RBP_ID_6652795,Human_RBP_ID_8823694,Human_RBP_ID_17693387,Human_RBP_ID_17903270,Human_RBP_ID_18297156,Human_RBP_ID_22959309,Human_RBP_ID_26975496 Human_Splice_Rec_1884434,Human_Splice_Rec_1884518 Human_miRNA_ID_2496713,Human_miRNA_ID_2497939 RMVar_hsa_circ_100717,RMVar_hsa_circ_187853,RMVar_hsa_circ_94994,RMVar_hsa_circ_117405,RMVar_hsa_circ_125032,RMVar_hsa_circ_125708,RMVar_hsa_circ_121551,RMVar_hsa_circ_113795,RMVar_hsa_circ_106229,RMVar_hsa_circ_109780,RMVar_hsa_circ_98640,RMVar_hsa_circ_76003,RMVar_hsa_circ_90191,RMVar_hsa_circ_187855,RMVar_hsa_circ_187857,RMVar_hsa_circ_187856,RMVar_hsa_circ_187854,RMVar_hsa_circ_187849,RMVar_hsa_circ_187851,RMVar_hsa_circ_187852,RMVar_hsa_circ_187850,RMVar_hsa_circ_187847,RMVar_hsa_circ_187848,RMVar_hsa_circ_82665,RMVar_hsa_circ_187859,RMVar_hsa_circ_187860 112699 RMVar_ID_112699 Human_SNP_ID_829357555 m1A Human chr17 + 19188100 19188100 19188100 CTGAACGTGTAGAGCACCGAAAACCACGAGGAAGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC CTGAACGTGTAGAGCACCGAAAACCACGAGGAGGAGAGGTAGCGTTTTCTCCTGAGCGTGAAGCC A G SNORD3A Ensembl:ENSG00000263934 snoRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:19187996..19188211 26863196 MeRIP-seq:(Medium) rs531318002 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_238474,Human_RBP_ID_269811,Human_RBP_ID_484667,Human_RBP_ID_768807,Human_RBP_ID_822902,Human_RBP_ID_905432,Human_RBP_ID_1180498,Human_RBP_ID_1547070,Human_RBP_ID_1850623,Human_RBP_ID_2528976,Human_RBP_ID_3514500,Human_RBP_ID_4467770,Human_RBP_ID_5088616,Human_RBP_ID_5098760,Human_RBP_ID_5189046,Human_RBP_ID_5291691,Human_RBP_ID_5496630,Human_RBP_ID_5576867,Human_RBP_ID_5649293,Human_RBP_ID_6567189,Human_RBP_ID_8194064,Human_RBP_ID_8253214,Human_RBP_ID_8446159,Human_RBP_ID_8727787,Human_RBP_ID_8826169,Human_RBP_ID_9069646,Human_RBP_ID_9258381,Human_RBP_ID_9290531,Human_RBP_ID_9341072,Human_RBP_ID_9424690,Human_RBP_ID_9883965,Human_RBP_ID_10483700,Human_RBP_ID_12917156,Human_RBP_ID_17063097,Human_RBP_ID_17081254,Human_RBP_ID_17126240,Human_RBP_ID_17189342,Human_RBP_ID_17207303,Human_RBP_ID_17264449,Human_RBP_ID_17495448,Human_RBP_ID_17567286,Human_RBP_ID_17582786,Human_RBP_ID_17610219,Human_RBP_ID_17670043,Human_RBP_ID_17673516,Human_RBP_ID_17693558,Human_RBP_ID_17886676,Human_RBP_ID_18165073,Human_RBP_ID_18174163,Human_RBP_ID_18200110,Human_RBP_ID_18207747,Human_RBP_ID_18488151,Human_RBP_ID_18513486,Human_RBP_ID_18530491,Human_RBP_ID_18544469,Human_RBP_ID_18691021,Human_RBP_ID_18926827,Human_RBP_ID_18943910,Human_RBP_ID_19087054,Human_RBP_ID_20292384,Human_RBP_ID_21960120,Human_RBP_ID_22055818,Human_RBP_ID_22210338,Human_RBP_ID_22358467,Human_RBP_ID_22370845,Human_RBP_ID_22372821,Human_RBP_ID_22425655,Human_RBP_ID_22524083,Human_RBP_ID_22531575,Human_RBP_ID_22544893,Human_RBP_ID_22660806,Human_RBP_ID_22705807,Human_RBP_ID_22717716,Human_RBP_ID_22741177,Human_RBP_ID_22762311,Human_RBP_ID_22803410,Human_RBP_ID_22947669,Human_RBP_ID_23111584,Human_RBP_ID_23114556,Human_RBP_ID_23119046,Human_RBP_ID_23128951,Human_RBP_ID_23276778,Human_RBP_ID_23308774,Human_RBP_ID_23714738,Human_RBP_ID_24417511,Human_RBP_ID_24532369,Human_RBP_ID_24545264,Human_RBP_ID_24552546,Human_RBP_ID_24559538,Human_RBP_ID_25338481,Human_RBP_ID_26460318,Human_RBP_ID_26575766,Human_RBP_ID_26640207,Human_RBP_ID_26749040,Human_RBP_ID_26783108,Human_RBP_ID_26956322,Human_RBP_ID_27250856,Human_RBP_ID_27449494,Human_RBP_ID_27560775,Human_RBP_ID_27572931,Human_RBP_ID_27796892 112700 RMVar_ID_112700 Human_SNP_ID_829365184 m1A Human chr17 - 64130107 64130107 64130107 CTAGTCAGTTCTGCGTCCGCTGAGGCTCGGTCACCGCCTCGCTGTCGTCGCGGCGCCCCCGCCCC CTAGTCAGTTCTGCGTCCGCTGAGGCTCGGTCGCCGCCTCGCTGTCGTCGCGGCGCCCCCGCCCC T C ERN1 Ensembl:ENSG00000178607 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64130058..64130130 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_4445352 RMVar_hsa_circ_112217,RMVar_hsa_circ_186400 112701 RMVar_ID_112701 Human_SNP_ID_829373882 m1A Human chr17 - 82060053 82060053 82060053 AGGGGAGCAAGGAGAAGGCAGGTGCGCGCAGCAAGCGGGCCCTGGAGGAAGAGGAGGGTGGCACG AGGGGAGCAAGGAGAAGGCAGGTGCGCGCAGCGAGCGGGCCCTGGAGGAAGAGGAGGGTGGCACG T C DUS1L Ensembl:ENSG00000169718 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:82060051..82060100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_236661,Human_RBP_ID_822066,Human_RBP_ID_898950,Human_RBP_ID_3951445,Human_RBP_ID_4460971,Human_RBP_ID_5368658,Human_RBP_ID_9377160,Human_RBP_ID_18470205,Human_RBP_ID_18993041,Human_RBP_ID_22657100 Human_Splice_Rec_1884212,Human_Splice_Rec_1884234,Human_Splice_Rec_1884262,Human_Splice_Rec_1884276,Human_Splice_Rec_1884292 RMVar_hsa_circ_80373,RMVar_hsa_circ_187845 112702 RMVar_ID_112702 Human_SNP_ID_829379091 m1A Human chr17 - 76500256 76500256 76500256 GAGTGTTGTTGTTACTGGCAGGTAGTGGGTAGAGGCCAGGGACGCTACCAGACATCTTCAGGGCA GAGTGTTGTTGTTACTGGCAGGTAGTGGGTAGGGGCCAGGGACGCTACCAGACATCTTCAGGGCA T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76500253..76500320 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_3545782,Human_RBP_ID_8189914,Human_RBP_ID_8727137 112703 RMVar_ID_112703 Human_SNP_ID_829380417 m1A Human chr17 - 7495927 7495924 7495928 CCGTCACAGACATTCGCTTCTGCAAAGAAAGAAAGGCCAACAACTGAACAGCGTTCCTAGTTTCT CCGTCACAGACATTCGCTTCTGCAAAGAAAG____GCCAACAACTGAACAGCGTTCCTAGTTTCT CCTTT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:7495926..7496000 26863196 MeRIP-seq:(Medium) rs3216887 Functional Loss DEL ICGC 32..35 33 PBCA 1 - 112704 RMVar_ID_112704 Human_SNP_ID_829385672 m1A Human chr17 + 63819878 63819878 63819878 CTCTTTGGTCCTTCTTCATCCTTGAGTCCACCACCTTGAAATGACCTCTGACTCCAGCTGGCCGG CTCTTTGGTCCTTCTTCATCCTTGAGTCCACCCCCTTGAAATGACCTCTGACTCCAGCTGGCCGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:63819726..63820399 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 112705 RMVar_ID_112705 Human_SNP_ID_829390465 m1A Human chr17 - 44209476 44209475 44209476 GTCCAATGGGGAGCTGAACCACCTGCCGCTGAAGGAGCGCATGGTGGAGATCGGCAGTCGCTGGC GTCCAATGGGGAGCTGAACCACCTGCCGCTGA_GGAGCGCATGGTGGAGATCGGCAGTCGCTGGC CT C UBTF Ensembl:ENSG00000108312 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:44209426..44209500 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUSC 1 - Human_RBP_ID_897654,Human_RBP_ID_4430820,Human_RBP_ID_8824727,Human_RBP_ID_9290118,Human_RBP_ID_9376127,Human_RBP_ID_26330769,Human_RBP_ID_26962533,Human_RBP_ID_27812754 Human_Splice_Rec_1825248,Human_Splice_Rec_1825288,Human_Splice_Rec_1825328,Human_Splice_Rec_1825366,Human_Splice_Rec_1825404,Human_Splice_Rec_1825442,Human_Splice_Rec_1825478,Human_Splice_Rec_1825516,Human_Splice_Rec_1825536,Human_Splice_Rec_1825544 RMVar_hsa_circ_89406,RMVar_hsa_circ_48784,RMVar_hsa_circ_184666 112706 RMVar_ID_112706 Human_SNP_ID_829391782 m1A Human chr17 - 40027948 40027948 40027948 CCTGGTCAATGCAGCCTGTCTCCATTCCTTTCAGTTTGAATGAATTCACAACCTATGGCAGCGAA CCTGGTCAATGCAGCCTGTCTCCATTCCTTTCGGTTTGAATGAATTCACAACCTATGGCAGCGAA T C MED24 Ensembl:ENSG00000008838 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:40027469..40027954 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 6 breast Human_RBP_ID_46729,Human_RBP_ID_22658744 Human_Splice_Rec_1813263,Human_Splice_Rec_1813311,Human_Splice_Rec_1813361,Human_Splice_Rec_1813409,Human_Splice_Rec_1813471,Human_Splice_Rec_1813535,Human_Splice_Rec_1813591,Human_Splice_Rec_1813635,Human_Splice_Rec_1813645,Human_Splice_Rec_1813659,Human_Splice_Rec_1813683 RMVar_hsa_circ_94153,RMVar_hsa_circ_184002,RMVar_hsa_circ_113893,RMVar_hsa_circ_184000,RMVar_hsa_circ_265673,RMVar_hsa_circ_324597 112707 RMVar_ID_112707 Human_SNP_ID_829399794 m1A Human chr17 - 40289355 40289355 40289355 GGACAACTAGTCAATATGTGAAAGTGAAGAGAAAATAACTAACATGGAATTTATTTATACTGATG GGACAACTAGTCAATATGTGAAAGTGAAGAGACAATAACTAACATGGAATTTATTTATACTGATG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:40289352..40289638 26863196 MeRIP-seq:(Medium) rs4134999 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112708 RMVar_ID_112708 Human_SNP_ID_829400427 m1A Human chr17 - 7193710 7193710 7193710 CCCTTGCAGATGCCCCACCTCCCACCAGGTCGAGAAGACTCGGTTCTGAGCTACGAGACAGTGAC CCCTTGCAGATGCCCCACCTCCCACCAGGTCGTGAAGACTCGGTTCTGAGCTACGAGACAGTGAC T A DLG4 Ensembl:ENSG00000132535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7193695..7196259 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_22655746 Human_Splice_Rec_1769330,Human_Splice_Rec_1769331,Human_Splice_Rec_1769370,Human_Splice_Rec_1769371,Human_Splice_Rec_1769412,Human_Splice_Rec_1769413,Human_Splice_Rec_1769452,Human_Splice_Rec_1769453,Human_Splice_Rec_1769486,Human_Splice_Rec_1769487,Human_Splice_Rec_1769526,Human_Splice_Rec_1769527,Human_Splice_Rec_1769560,Human_Splice_Rec_1769561,Human_Splice_Rec_1769594,Human_Splice_Rec_1769595,Human_Splice_Rec_1769630,Human_Splice_Rec_1769631,Human_Splice_Rec_1769670,Human_Splice_Rec_1769671,Human_Splice_Rec_1769690,Human_Splice_Rec_1769691,Human_Splice_Rec_1769726,Human_Splice_Rec_1769727,Human_Splice_Rec_1769754,Human_Splice_Rec_1769755 RMVar_hsa_circ_266955 112709 RMVar_ID_112709 Human_SNP_ID_829401019 m1A Human chr17 + 38510038 38510038 38510038 GGCCGTCAACCGCAAGCGCAAGAAGCGGCGGGAGGCGCGGGGGCTGGGCAGCAGCACCGACGACG GGCCGTCAACCGCAAGCGCAAGAAGCGGCGGGGGGCGCGGGGGCTGGGCAGCAGCACCGACGACG A G ARHGAP23 Ensembl:ENSG00000275832 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38509989..38510082 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_1809434,Human_Splice_Rec_1809482,Human_Splice_Rec_1809534,Human_Splice_Rec_1809542 112710 RMVar_ID_112710 Human_SNP_ID_829403567 m1A Human chr17 + 82101597 82101597 82101597 CTCCCTGCCTCCACCCTGCACGCTGTGCCCACACCCCCCCACAACACGTAGGTGAAAGCACAGGC CTCCCTGCCTCCACCCTGCACGCTGTGCCCACCCCCCCCCACAACACGTAGGTGAAAGCACAGGC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:82101559..82101660 32194978 MeRIP-seq:(Medium) rs755270994 Functional Loss SNV ICGC 33..33 33 CHOL 1 - 112711 RMVar_ID_112711 Human_SNP_ID_829407665 m1A Human chr17 + 5373380 5373379 5373380 AAGAGCTGGTGAGGTTACAGAAAGATAATGACAGTCTCCAGGGAAAGCACAGCCTGCATGTGTCA AAGAGCTGGTGAGGTTACAGAAAGATAATGAC_GTCTCCAGGGAAAGCACAGCCTGCATGTGTCA CA C RABEP1 Ensembl:ENSG00000029725 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:5361262..5377206 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BRCA 1 - Human_RBP_ID_46836,Human_RBP_ID_6614693,Human_RBP_ID_8819879,Human_RBP_ID_9377417 Human_Splice_Rec_1766632,Human_Splice_Rec_1766633,Human_Splice_Rec_1766664,Human_Splice_Rec_1766665,Human_Splice_Rec_1766692,Human_Splice_Rec_1766693 RMVar_hsa_circ_78581,RMVar_hsa_circ_181611,RMVar_hsa_circ_181608,RMVar_hsa_circ_126806,RMVar_hsa_circ_72658,RMVar_hsa_circ_345775,RMVar_hsa_circ_341427,RMVar_hsa_circ_10897,RMVar_hsa_circ_53460,RMVar_hsa_circ_105668,RMVar_hsa_circ_331716,RMVar_hsa_circ_181619,RMVar_hsa_circ_355715,RMVar_hsa_circ_301614,RMVar_hsa_circ_181627,RMVar_hsa_circ_14749,RMVar_hsa_circ_285585,RMVar_hsa_circ_329979,RMVar_hsa_circ_33423,RMVar_hsa_circ_181630,RMVar_hsa_circ_181631,RMVar_hsa_circ_181632,RMVar_hsa_circ_62379,RMVar_hsa_circ_86322,RMVar_hsa_circ_375697,RMVar_hsa_circ_181633,RMVar_hsa_circ_285866,RMVar_hsa_circ_181634,RMVar_hsa_circ_181636,RMVar_hsa_circ_181635,RMVar_hsa_circ_181638,RMVar_hsa_circ_41499,RMVar_hsa_circ_363482 112712 RMVar_ID_112712 Human_SNP_ID_829408118 m1A Human chr17 - 42668240 42668240 42668240 ACTTGGCCAACCCCTCCCCCGAGAGGCCCTGCAGCAGCTCTTCTCCTCCATGCCAAGACCTGCCA ACTTGGCCAACCCCTCCCCCGAGAGGCCCTGCTGCAGCTCTTCTCCTCCATGCCAAGACCTGCCA T A PLEKHH3 Ensembl:ENSG00000068137 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42668120..42668299 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_1368373 Human_Splice_Rec_1820200,Human_Splice_Rec_1820224,Human_Splice_Rec_1820248,Human_Splice_Rec_1820272,Human_Splice_Rec_1820316 Human_miRNA_ID_1061801,Human_miRNA_ID_2370789,Human_miRNA_ID_2707073 RMVar_hsa_circ_96929,RMVar_hsa_circ_184441 112713 RMVar_ID_112713 Human_SNP_ID_829408847 m1A Human chr17 + 44967539 44967539 44967539 AGGACATGGTAGGTGAAAAAGTAGGTGCCGGGAATGTTGCACGTAAACTTGCCGCTGGCCGCGTC AGGACATGGTAGGTGAAAAAGTAGGTGCCGGGGATGTTGCACGTAAACTTGCCGCTGGCCGCGTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:44967446..44967755 26863196 MeRIP-seq:(Medium) rs748894893 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 112714 RMVar_ID_112714 Human_SNP_ID_829409558 m1A Human chr17 + 81531891 81531886 81531891 TGATGGCGATGATGGTGATGATGGTGATGGCGATGATGGTGATAGTGATGGTGATGATGGTGATG TGATGGCGATGATGGTGATGATGGTGAT_____TGATGGTGATAGTGATGGTGATGATGGTGATG TGGCGA T FSCN2 Ensembl:ENSG00000186765 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81531362..81532095 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 29..33 33 SKCA 1 - Human_RBP_ID_23754630 112715 RMVar_ID_112715 Human_SNP_ID_829415235 m1A Human chr17 + 79839047 79839047 79839047 GCGACCAGCCTCTCCATTTCACCAGATACTCCACTCTGCCCTGGGGGGAAGAGACAGCACTCCAT GCGACCAGCCTCTCCATTTCACCAGATACTCCCCTCTGCCCTGGGGGGAAGAGACAGCACTCCAT A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:79837766..79839441 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 112716 RMVar_ID_112716 Human_SNP_ID_829418003 m1A Human chr17 + 6608461 6608461 6608461 TCTCTGGGGCTAGTTTTCACCTTTAGCCATGCAGCACTGAAATAAATGGAAAAGCATACCTTTGT TCTCTGGGGCTAGTTTTCACCTTTAGCCATGCGGCACTGAAATAAATGGAAAAGCATACCTTTGT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:6608459..6608586 26863196 MeRIP-seq:(Medium) rs4796519 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 8 large intestine,haematopoietic and lymphoid tissue GWAS_ID_13510,GWAS_ID_13511,GWAS_ID_13512,GWAS_ID_13513,GWAS_ID_13514,GWAS_ID_13515,GWAS_ID_13516,GWAS_ID_13517,GWAS_ID_13518,GWAS_ID_13519,GWAS_ID_13520,GWAS_ID_13521,GWAS_ID_13522,GWAS_ID_13523,GWAS_ID_13524,GWAS_ID_13525,GWAS_ID_13526,GWAS_ID_13527,GWAS_ID_13528,GWAS_ID_13529,GWAS_ID_13530,GWAS_ID_13531,GWAS_ID_13532,GWAS_ID_13533,GWAS_ID_13534,GWAS_ID_13535,GWAS_ID_13536,GWAS_ID_13537,GWAS_ID_13538,GWAS_ID_13539,GWAS_ID_13540,GWAS_ID_13541,GWAS_ID_13542,GWAS_ID_13543,GWAS_ID_13544,GWAS_ID_13545,GWAS_ID_13546,GWAS_ID_13547,GWAS_ID_13548,GWAS_ID_13549,GWAS_ID_13550,GWAS_ID_13551,GWAS_ID_13552,GWAS_ID_13553,GWAS_ID_13554,GWAS_ID_13555,GWAS_ID_13556,GWAS_ID_13557,GWAS_ID_13558,GWAS_ID_13559,GWAS_ID_13560 112717 RMVar_ID_112717 Human_SNP_ID_829420068 m1A Human chr17 - 41689814 41689814 41689814 TTATATGGATATAATCCTCAGTGCCAGCAGGAAGCAGGTCATCACCCTTACTTGCATCAGCAAAG TTATATGGATATAATCCTCAGTGCCAGCAGGACGCAGGTCATCACCCTTACTTGCATCAGCAAAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:41689801..41689825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_94813,RMVar_hsa_circ_117561,RMVar_hsa_circ_109153,RMVar_hsa_circ_96493,RMVar_hsa_circ_107266,RMVar_hsa_circ_184127,RMVar_hsa_circ_184129,RMVar_hsa_circ_184128,RMVar_hsa_circ_184126,RMVar_hsa_circ_184130 112718 RMVar_ID_112718 Human_SNP_ID_829424465 m1A Human chr17 + 78971509 78971507 78971510 GTTGAAGGTCATTGCAGAGAGGAAGGAAGCCGAGGAGGGGAGCCTGCAGTGAGGGCGTCCTGGGG GTTGAAGGTCATTGCAGAGAGGAAGGAAGCC___GAGGGGAGCCTGCAGTGAGGGCGTCCTGGGG CGAG C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr17:78971411..78971540 26863196 MeRIP-seq:(Medium) rs1393875423 Functional Loss DEL TCGA 32..34 33 STAD 1 - 112719 RMVar_ID_112719 Human_SNP_ID_829431000 m1A Human chr17 + 81457591 81457591 81457591 GCCAAGAAGAAGAAGGAGAGGCAGGGGTTGCTAGGTAACCAGGAGGGAGGACAGGGGTTGCTAGG GCCAAGAAGAAGAAGGAGAGGCAGGGGTTGCTGGGTAACCAGGAGGGAGGACAGGGGTTGCTAGG A G BAHCC1 Ensembl:ENSG00000266074 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:81457394..81457618 26863196 MeRIP-seq:(Medium) rs1332849611 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_Splice_Rec_1880861,Human_Splice_Rec_1880909,Human_Splice_Rec_1880935 RMVar_hsa_circ_265942 112720 RMVar_ID_112720 Human_SNP_ID_829433121 m1A Human chr17 + 4945155 4945155 4945155 CACACCTATCCTTTTGAGGGGCTTTGGGGTGGAGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT CACACCTATCCTTTTGAGGGGCTTTGGGGTGGGGCTGGGGCAAGCAGAGGGACTGGGTCTTCACT A G RNF167 Ensembl:ENSG00000108523 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs6559 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 5 liver Human_RBP_ID_493341,Human_RBP_ID_822314,Human_RBP_ID_1009088,Human_RBP_ID_5115336,Human_RBP_ID_6611354,Human_RBP_ID_8819593,Human_RBP_ID_17895688,Human_RBP_ID_18941236,Human_RBP_ID_22499821,Human_RBP_ID_22805498 Human_miRNA_ID_2210755,Human_miRNA_ID_2956311 GWAS_ID_13456,GWAS_ID_13457,GWAS_ID_13458,GWAS_ID_13459,GWAS_ID_13460 RMVar_hsa_circ_181541,RMVar_hsa_circ_98162,RMVar_hsa_circ_126141,RMVar_hsa_circ_77277,RMVar_hsa_circ_181542,RMVar_hsa_circ_122770,RMVar_hsa_circ_181543,RMVar_hsa_circ_81003,RMVar_hsa_circ_112728,RMVar_hsa_circ_181544,RMVar_hsa_circ_75912,RMVar_hsa_circ_181545,RMVar_hsa_circ_181546,RMVar_hsa_circ_96484,RMVar_hsa_circ_181547,RMVar_hsa_circ_181550 112721 RMVar_ID_112721 Human_SNP_ID_829433718 m1A Human chr17 - 38297251 38297251 38297251 CCCCTAGGGTCCTATCGGCCCCGTCCCTACCCACCTGCCGAGACCACCAGCCCAAAAACCTCGAT CCCCTAGGGTCCTATCGGCCCCGTCCCTACCCCCCTGCCGAGACCACCAGCCCAAAAACCTCGAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38297211..38297295 26863196 MeRIP-seq:(Medium) rs758842244 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112722 RMVar_ID_112722 Human_SNP_ID_829436658 m1A Human chr17 - 19738125 19738125 19738125 GGCTCTCCTGGCCCTGGGAGAATCGCTCCTGCAGCCCCAGCCCAGCCCCACTCCTCTGCTGACCT GGCTCTCCTGGCCCTGGGAGAATCGCTCCTGCCGCCCCAGCCCAGCCCCACTCCTCTGCTGACCT T G ALDH3A1 Ensembl:ENSG00000108602 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:19738074..19738179;chr17:19738076..19738175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach RMVar_hsa_circ_78958,RMVar_hsa_circ_182594 112723 RMVar_ID_112723 Human_SNP_ID_829449141 m1A Human chr17 + 43196972 43196972 43196972 AGATTCTATGGTGTCAGTAAAGAGGAAGGCTGAGAACATTGCTTCTGTGGAGGAAGCAGAAGAAG AGATTCTATGGTGTCAGTAAAGAGGAAGGCTGCGAACATTGCTTCTGTGGAGGAAGCAGAAGAAG A C NBR1 Ensembl:ENSG00000188554 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:43196103..43197013 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_766629,Human_RBP_ID_822722,Human_RBP_ID_3950688,Human_RBP_ID_9257874,Human_RBP_ID_17892948,Human_RBP_ID_22063161,Human_RBP_ID_26331854 Human_Splice_Rec_1823010,Human_Splice_Rec_1823052,Human_Splice_Rec_1823088,Human_Splice_Rec_1823130 RMVar_hsa_circ_67132,RMVar_hsa_circ_312168,RMVar_hsa_circ_317334,RMVar_hsa_circ_73235,RMVar_hsa_circ_184570,RMVar_hsa_circ_24888,RMVar_hsa_circ_372724,RMVar_hsa_circ_360991,RMVar_hsa_circ_111325,RMVar_hsa_circ_184571,RMVar_hsa_circ_184573,RMVar_hsa_circ_328568,RMVar_hsa_circ_19491,RMVar_hsa_circ_339976,RMVar_hsa_circ_314795,RMVar_hsa_circ_184572 112724 RMVar_ID_112724 Human_SNP_ID_829455203 m1A Human chr17 + 62671735 62671735 62671735 GCCACTGCTACCGCCTGCAGGCCGAGAAGCGCAGCTGGCAGGAGTCCAAGAAGGCATGTCTACGG GCCACTGCTACCGCCTGCAGGCCGAGAAGCGCTGCTGGCAGGAGTCCAAGAAGGCATGTCTACGG A T MRC2 Ensembl:ENSG00000011028 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:62671560..62671775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_Splice_Rec_1850812,Human_Splice_Rec_1850870 RMVar_hsa_circ_70974,RMVar_hsa_circ_10784,RMVar_hsa_circ_186230,RMVar_hsa_circ_308737,RMVar_hsa_circ_372334,RMVar_hsa_circ_114480,RMVar_hsa_circ_37407,RMVar_hsa_circ_96956,RMVar_hsa_circ_27711,RMVar_hsa_circ_88864,RMVar_hsa_circ_186231,RMVar_hsa_circ_75968,RMVar_hsa_circ_186232,RMVar_hsa_circ_186233,RMVar_hsa_circ_75686,RMVar_hsa_circ_186234,RMVar_hsa_circ_186235,RMVar_hsa_circ_96114,RMVar_hsa_circ_186237,RMVar_hsa_circ_44124 112725 RMVar_ID_112725 Human_SNP_ID_829456542 m1A Human chr17 - 50185435 50185435 50185435 AACCAACTTTCCCCCCAACCCGGAAACAGACAAGCAACCCAAACTGAACCCCCTCAAAAGCCAAA AACCAACTTTCCCCCCAACCCGGAAACAGACACGCAACCCAAACTGAACCCCCTCAAAAGCCAAA T G COL1A1 Ensembl:ENSG00000108821 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:50185376..50185565 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_130760 Human_miRNA_ID_874529,Human_miRNA_ID_1560166 RMVar_hsa_circ_83975,RMVar_hsa_circ_99122,RMVar_hsa_circ_107914,RMVar_hsa_circ_107980,RMVar_hsa_circ_123094,RMVar_hsa_circ_100414,RMVar_hsa_circ_90931,RMVar_hsa_circ_98517,RMVar_hsa_circ_89515,RMVar_hsa_circ_185251,RMVar_hsa_circ_185255,RMVar_hsa_circ_76245,RMVar_hsa_circ_77039,RMVar_hsa_circ_185257,RMVar_hsa_circ_185258,RMVar_hsa_circ_185259,RMVar_hsa_circ_185256,RMVar_hsa_circ_185253,RMVar_hsa_circ_185254,RMVar_hsa_circ_185252,RMVar_hsa_circ_185249,RMVar_hsa_circ_185250 112726 RMVar_ID_112726 Human_SNP_ID_829465143 m1A Human chr17 + 7594295 7594295 7594295 TTATCACCTTCCACTCGAACCCTCACCACACCAGATTTATCCACAATCTCCTGGATCACTTTCCC TTATCACCTTCCACTCGAACCCTCACCACACCGGATTTATCCACAATCTCCTGGATCACTTTCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:7594196..7594374 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_1289120,Human_RBP_ID_3538105 112727 RMVar_ID_112727 Human_SNP_ID_829473647 m1A Human chr17 + 58495518 58495518 58495518 CCAATGGCATTTTCCCAAAGCGAGGATTTTCCAATAACTGCCCATTCCTATTATTTCCTCTTTTA CCAATGGCATTTTCCCAAAGCGAGGATTTTCCTATAACTGCCCATTCCTATTATTTCCTCTTTTA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:58495469..58504312 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 112728 RMVar_ID_112728 Human_SNP_ID_829479231 m1A Human chr17 + 64506230 64506230 64506230 CGGCGAAGCCTTGCGGGGGCGGCAGCGGAGGAAGGACACCGATGACACCAGCCGAAGCTGCACTA CGGCGAAGCCTTGCGGGGGCGGCAGCGGAGGACGGACACCGATGACACCAGCCGAAGCTGCACTA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:64506126..64506300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - 112729 RMVar_ID_112729 Human_SNP_ID_829487353 m1A Human chr17 - 81845151 81845151 81845151 CCTGGAGAGCGGTGGCCAGGATGGGGCAGGGGATGATGACGTGAGTGGGGTCACAGCCCTGGGCT CCTGGAGAGCGGTGGCCAGGATGGGGCAGGGGTTGATGACGTGAGTGGGGTCACAGCCCTGGGCT T A P4HB Ensembl:ENSG00000185624 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:81843626..81845151 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_237043,Human_RBP_ID_820464,Human_RBP_ID_902043,Human_RBP_ID_6651950,Human_RBP_ID_17654385,Human_RBP_ID_17902925,Human_RBP_ID_22444018,Human_RBP_ID_22760995,Human_RBP_ID_22958333,Human_RBP_ID_23129876,Human_RBP_ID_23755120,Human_RBP_ID_26460039 Human_Splice_Rec_1882010,Human_Splice_Rec_1882011,Human_Splice_Rec_1882022,Human_Splice_Rec_1882023,Human_Splice_Rec_1882042,Human_Splice_Rec_1882043,Human_Splice_Rec_1882049,Human_Splice_Rec_1882052,Human_Splice_Rec_1882053,Human_Splice_Rec_1882060,Human_Splice_Rec_1882061,Human_Splice_Rec_1882078,Human_Splice_Rec_1882079,Human_Splice_Rec_1882086,Human_Splice_Rec_1882087 RMVar_hsa_circ_96174,RMVar_hsa_circ_118621,RMVar_hsa_circ_124594,RMVar_hsa_circ_187763,RMVar_hsa_circ_100494,RMVar_hsa_circ_104101,RMVar_hsa_circ_187765,RMVar_hsa_circ_95248,RMVar_hsa_circ_187764,RMVar_hsa_circ_187761,RMVar_hsa_circ_187762,RMVar_hsa_circ_127116,RMVar_hsa_circ_187767,RMVar_hsa_circ_187768,RMVar_hsa_circ_187769 112730 RMVar_ID_112730 Human_SNP_ID_829487687 m1A Human chr17 + 4704075 4704075 4704075 ACCCCCGGTCCCGCCAGGAACCCCAGCCGCGGAGCCCGCAGAGGGCCCACTCAGAACGGCTGCCG ACCCCCGGTCCCGCCAGGAACCCCAGCCGCGGCGCCCGCAGAGGGCCCACTCAGAACGGCTGCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:4703981..4704075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 112731 RMVar_ID_112731 Human_SNP_ID_829491220 m1A Human chr17 - 48596397 48596396 48596397 AAAAACAGGCCGAGTGAAGGTGCTGGAAAGGGAGGGAGGACGCGAGGGGAAAGGCCTGTGGGGAG AAAAACAGGCCGAGTGAAGGTGCTGGAAAGGG_GGGAGGACGCGAGGGGAAAGGCCTGTGGGGAG CT C HOXB3,HOXB6 Ensembl:ENSG00000120093,Ensembl:ENSG00000108511 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48596349..48596566 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - Human_RBP_ID_22715756,Human_RBP_ID_25296200,Human_RBP_ID_26964758 112732 RMVar_ID_112732 Human_SNP_ID_829495242 m1A Human chr17 + 2692075 2692075 2692075 CAGGGCCGACCGGAACTCAGCTTTGCTCTCGTAGACTCGGGCGACAAGGTGGTGGCTGCCGGGAG CAGGGCCGACCGGAACTCAGCTTTGCTCTCGTGGACTCGGGCGACAAGGTGGTGGCTGCCGGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:2692026..2692075 32194978 MeRIP-seq:(Medium) rs748480811 Functional Loss SNV ICGC 33..33 33 THCA 1 - 112733 RMVar_ID_112733 Human_SNP_ID_829509582 m1A Human chr17 - 49413277 49413277 49413277 TTGTTTTTATCCCCTTAGGTGTGAGAGGGTCCAGCAGAAGGAAACATGGCTGCCAAAGTGTTTGA TTGTTTTTATCCCCTTAGGTGTGAGAGGGTCCGGCAGAAGGAAACATGGCTGCCAAAGTGTTTGA T C PHB Ensembl:ENSG00000167085 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:49413226..49413300 32194978 MeRIP-seq:(Medium) rs749139558 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_236573,Human_RBP_ID_821226,Human_RBP_ID_903588,Human_RBP_ID_4466565,Human_RBP_ID_5114751,Human_RBP_ID_5364541,Human_RBP_ID_9327351,Human_RBP_ID_17654261,Human_RBP_ID_22444747,Human_RBP_ID_23210031 Human_Splice_Rec_1835730,Human_Splice_Rec_1835744,Human_Splice_Rec_1835756,Human_Splice_Rec_1835764,Human_Splice_Rec_1835780,Human_Splice_Rec_1835792,Human_Splice_Rec_1835820,Human_Splice_Rec_1835830,Human_Splice_Rec_1835844,Human_Splice_Rec_1835852 RMVar_hsa_circ_6832,RMVar_hsa_circ_95959,RMVar_hsa_circ_112783,RMVar_hsa_circ_185166,RMVar_hsa_circ_185167,RMVar_hsa_circ_185169,RMVar_hsa_circ_105225 112734 RMVar_ID_112734 Human_SNP_ID_829515177 m1A Human chr17 + 6118102 6118102 6118102 GATGTTTGATTCAGCCATCCTGCTAATCCGGAACCCATACAGGTCCCTGGTGGCAGAATTCAACA GATGTTTGATTCAGCCATCCTGCTAATCCGGACCCCATACAGGTCCCTGGTGGCAGAATTCAACA A C WSCD1 Ensembl:ENSG00000179314 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:6118051..6118129 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas Human_Splice_Rec_1767653,Human_Splice_Rec_1767667,Human_Splice_Rec_1767687,Human_Splice_Rec_1767703,Human_Splice_Rec_1767719,Human_Splice_Rec_1767735 RMVar_hsa_circ_265344,RMVar_hsa_circ_181708 112735 RMVar_ID_112735 Human_SNP_ID_829516538 m1A Human chr17 + 3680466 3680466 3680466 ACCCTGCATCCTCCACCCTGAGTCCTCCACCCAGTGTCCTCCACCCTGCATCCTCCACCCAGTGT ACCCTGCATCCTCCACCCTGAGTCCTCCACCCGGTGTCCTCCACCCTGCATCCTCCACCCAGTGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:3680462..3680622 26863196 MeRIP-seq:(Medium) rs112686978 Functional Loss SNV ICGC,COSMIC 33..33 33 LUSC,head_neck squamous_cell_carcinoma 7 head and neck 112736 RMVar_ID_112736 Human_SNP_ID_829520511 m1A Human chr17 + 40363067 40363067 40363067 CGCACGGCTCGGGGCCGGGGCGCCGGGAGGGCAGGGCCGGTGGCGGAGGTGGCGGCGGCGGCGGC CGCACGGCTCGGGGCCGGGGCGCCGGGAGGGCGGGGCCGGTGGCGGAGGTGGCGGCGGCGGCGGC A G AC080112.2 Ensembl:ENSG00000266208 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:40362889..40363335 26863196 MeRIP-seq:(Medium) rs1476943010 Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_819692,Human_RBP_ID_4466383 112737 RMVar_ID_112737 Human_SNP_ID_829527646 m1A Human chr17 - 4671456 4671456 4671456 GTCCCCCTGATGATGAGAAGCCACCACCTCCCACAGAGCCTGACTCCTAGCCATCTTCTGCACCC GTCCCCCTGATGATGAGAAGCCACCACCTCCCTCAGAGCCTGACTCCTAGCCATCTTCTGCACCC T A PELP1 Ensembl:ENSG00000141456 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9436 Functional Loss SNV ICGC 33..33 33 LUSC 3 - Human_RBP_ID_1860994,Human_RBP_ID_5577434,Human_RBP_ID_6605636,Human_RBP_ID_8455122,Human_RBP_ID_9375140,Human_RBP_ID_18700622,Human_RBP_ID_20172378,Human_RBP_ID_26330627,Human_RBP_ID_26964058,Human_RBP_ID_27813317 Human_Splice_Rec_1763728,Human_Splice_Rec_1763760,Human_Splice_Rec_1763792,Human_Splice_Rec_1763826,Human_Splice_Rec_1763856,Human_Splice_Rec_1763890 Human_miRNA_ID_3069833 GWAS_ID_13450,GWAS_ID_13451,GWAS_ID_13452,GWAS_ID_13453,GWAS_ID_13454 RMVar_hsa_circ_85238,RMVar_hsa_circ_103331,RMVar_hsa_circ_117433,RMVar_hsa_circ_118384,RMVar_hsa_circ_109133,RMVar_hsa_circ_100376,RMVar_hsa_circ_102442,RMVar_hsa_circ_87337,RMVar_hsa_circ_181482,RMVar_hsa_circ_181486,RMVar_hsa_circ_78929,RMVar_hsa_circ_83346,RMVar_hsa_circ_181488,RMVar_hsa_circ_181490,RMVar_hsa_circ_181491,RMVar_hsa_circ_181489,RMVar_hsa_circ_181487,RMVar_hsa_circ_181484,RMVar_hsa_circ_181485,RMVar_hsa_circ_181483 112738 RMVar_ID_112738 Human_SNP_ID_829530106 m1A Human chr17 - 1400163 1400163 1400163 CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGAGACACTATCCGCTTCCATCCGTCGCGCAGACC CCGGACGCGGAGCGAGAGGCTGAGAGAGTCGGCGACACTATCCGCTTCCATCCGTCGCGCAGACC T G YWHAE Ensembl:ENSG00000108953 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:1399994..1400225;chr17:1399804..1400225;chr17:1399907..1400225 26863196 MeRIP-seq:(Medium) rs868169662 Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_47626,Human_RBP_ID_764946,Human_RBP_ID_1284350,Human_RBP_ID_1527848,Human_RBP_ID_1848825,Human_RBP_ID_4405795,Human_RBP_ID_5189062,Human_RBP_ID_5419797,Human_RBP_ID_5466077,Human_RBP_ID_6559365,Human_RBP_ID_8253178,Human_RBP_ID_8444235,Human_RBP_ID_8813033,Human_RBP_ID_9327107,Human_RBP_ID_9375014,Human_RBP_ID_12888879,Human_RBP_ID_17691223,Human_RBP_ID_17885190,Human_RBP_ID_18689064,Human_RBP_ID_22060918,Human_RBP_ID_22803090,Human_RBP_ID_22946839,Human_RBP_ID_23711179,Human_RBP_ID_26330620,Human_RBP_ID_26954132 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 112739 RMVar_ID_112739 Human_SNP_ID_829533108 m1A Human chr17 + 50136145 50136145 50136145 TGCGCTCCTTGTTCTCCTCCACACTCTGCTCCAACTGCGCCTTCTCCACCCGCCAGCGCCCCTTC TGCGCTCCTTGTTCTCCTCCACACTCTGCTCCTACTGCGCCTTCTCCACCCGCCAGCGCCCCTTC A T AC002401.1 Ensembl:ENSG00000236472 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:50135951..50140275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 112740 RMVar_ID_112740 Human_SNP_ID_829534268 m1A Human chr17 + 50150760 50150760 50150760 CGCCTCCCCCAATCAAGCTGCCGAAGACAGCCAGCCCCGCTTCAAAAGCCCGAGCGGCCTGGTAC CGCCTCCCCCAATCAAGCTGCCGAAGACAGCCGGCCCCGCTTCAAAAGCCCGAGCGGCCTGGTAC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:50150709..50150914 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112741 RMVar_ID_112741 Human_SNP_ID_829535433 m1A Human chr17 + 58005966 58005966 58005966 TGATCCTTTAAATCCTGCCAACTTCCACTTGGAGGCAGTCCTGAAAAAGTGATTTTTTTTTTCTT TGATCCTTTAAATCCTGCCAACTTCCACTTGGGGGCAGTCCTGAAAAAGTGATTTTTTTTTTCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:58005846..58005975 26863196 MeRIP-seq:(Medium) rs763505486 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain 112742 RMVar_ID_112742 Human_SNP_ID_829538991 m1A Human chr17 + 19383193 19383193 19383193 CCCTGCAGCGTGAGATCCAGATGGACTCCCCAATGCTGCTGGCTGACCTGCCTGACCTCCAGGAC CCCTGCAGCGTGAGATCCAGATGGACTCCCCAGTGCTGCTGGCTGACCTGCCTGACCTCCAGGAC A G MAPK7 Ensembl:ENSG00000166484 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:19382117..19383344 32194978 MeRIP-seq:(Medium) rs757807560 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_27449554 112743 RMVar_ID_112743 Human_SNP_ID_829547148 m1A Human chr17 - 75763399 75763399 75763399 CTCCCTGGCTTCAGTGCAGTGGTGGTCAGCTCAGTGCCCCTGGGGGGTGGCCTGTCCAGCTCAGC CTCCCTGGCTTCAGTGCAGTGGTGGTCAGCTCCGTGCCCCTGGGGGGTGGCCTGTCCAGCTCAGC T G GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75763301..75763450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_499942,Human_RBP_ID_5467003,Human_RBP_ID_18190945,Human_RBP_ID_22443900 Human_Splice_Rec_1868814,Human_Splice_Rec_1868815,Human_Splice_Rec_1868842,Human_Splice_Rec_1868843,Human_Splice_Rec_1868856,Human_Splice_Rec_1868857,Human_Splice_Rec_1868866,Human_Splice_Rec_1868874 Human_miRNA_ID_172375,Human_miRNA_ID_2469806 RMVar_hsa_circ_126195,RMVar_hsa_circ_187089,RMVar_hsa_circ_83145,RMVar_hsa_circ_187090 112744 RMVar_ID_112744 Human_SNP_ID_829551009 m1A Human chr17 + 42957970 42957969 42957970 AGGAGGAACTATCAAGGAAGAGGGAACAAGACAGCCAAAGGCCTTAAGGAAGAAAGAAGTAGCGC AGGAGGAACTATCAAGGAAGAGGGAACAAGAC_GCCAAAGGCCTTAAGGAAGAAAGAAGTAGCGC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:42957968..42958053 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - 112745 RMVar_ID_112745 Human_SNP_ID_829562540 m1A Human chr17 - 75253716 75253716 75253716 TTCTTACCCTCCAGAAAAGCAGGAAAGGGGTCAGGGTGTGGAAATAAGGGATTGGGGCACACAGA TTCTTACCCTCCAGAAAAGCAGGAAAGGGGTCGGGGTGTGGAAATAAGGGATTGGGGCACACAGA T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:75253713..75253899 26863196 MeRIP-seq:(Medium) rs201074686 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine 112746 RMVar_ID_112746 Human_SNP_ID_829564891 m1A Human chr17 - 48728413 48728413 48728413 CCTTGGATCTGCCAGGCTCGGCGGAGCCGCCAAAGCAATGCCACCCATGCCCTGGGGTGCCCCAG CCTTGGATCTGCCAGGCTCGGCGGAGCCGCCAGAGCAATGCCACCCATGCCCTGGGGTGCCCCAG T C HOXB13 Ensembl:ENSG00000159184 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:48728335..48728517 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 112747 RMVar_ID_112747 Human_SNP_ID_829565936 m1A Human chr17 + 18184766 18184766 18184766 TCCCCGAGTGGGTGCACCAGCTGGTGATCCAAAAGCTGGTGGAGCACCGCGTCATCCCCGAGGGC TCCCCGAGTGGGTGCACCAGCTGGTGATCCAAGAGCTGGTGGAGCACCGCGTCATCCCCGAGGGC A G ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:18184251..18184900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_1006550,Human_RBP_ID_1528966,Human_RBP_ID_1850373,Human_RBP_ID_6565994,Human_RBP_ID_8813906,Human_RBP_ID_17886448,Human_RBP_ID_18190732,Human_RBP_ID_26811989,Human_RBP_ID_26956008,Human_RBP_ID_27250579 Human_miRNA_ID_2360173 RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 112748 RMVar_ID_112748 Human_SNP_ID_829566894 m1A Human chr17 + 8207838 8207838 8207838 ACTCGCTGGGGCAGGGTGCTCAGGCCAGATGGAGCCTGAGAAGGAGCAGGGGGTAGCTCTGAGGG ACTCGCTGGGGCAGGGTGCTCAGGCCAGATGGGGCCTGAGAAGGAGCAGGGGGTAGCTCTGAGGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:8207726..8207850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - 112749 RMVar_ID_112749 Human_SNP_ID_829567456 m1A Human chr17 - 49867147 49867147 49867147 ACCCACCTAATAATCTATCCATTCAACCATTCACCCTTATATCCATTTACCTAAACACCCACAAA ACCCACCTAATAATCTATCCATTCAACCATTCGCCCTTATATCCATTTACCTAAACACCCACAAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:49867055..49867319 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 112750 RMVar_ID_112750 Human_SNP_ID_829574656 m1A Human chr17 - 43124548 43124548 43124548 AACAGATGCTGCCGGCAGGGATGTGCTTGAGGAGGATCCAGAGATGAGAGCAGGTCACTGGGAAA AACAGATGCTGCCGGCAGGGATGTGCTTGAGGGGGATCCAGAGATGAGAGCAGGTCACTGGGAAA T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:43124526..43124726 26863196 MeRIP-seq:(Medium) rs191197821 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_237469,Human_RBP_ID_5088308,Human_RBP_ID_6596931,Human_RBP_ID_13015442 112751 RMVar_ID_112751 Human_SNP_ID_829575672 m1A Human chr17 + 39708497 39708497 39708497 AACAATACCACCCCTGTCACAGGGGCCTCCCCAGGAGGCCTGCGGGAGCTGCAGCTTCGAAGCCT AACAATACCACCCCTGTCACAGGGGCCTCCCCTGGAGGCCTGCGGGAGCTGCAGCTTCGAAGCCT A T ERBB2 Ensembl:ENSG00000141736 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:39708322..39708523 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 8 bladder,urinary tract Human_RBP_ID_902174,Human_RBP_ID_4424135 Human_Splice_Rec_1811893,Human_Splice_Rec_1811957,Human_Splice_Rec_1811985,Human_Splice_Rec_1812037,Human_Splice_Rec_1812129,Human_Splice_Rec_1812207,Human_Splice_Rec_1812259,Human_Splice_Rec_1812311,Human_Splice_Rec_1812329,Human_Splice_Rec_1812331 Human_miRNA_ID_205061,Human_miRNA_ID_254207,Human_miRNA_ID_842818,Human_miRNA_ID_1489634,Human_miRNA_ID_2013703,Human_miRNA_ID_2041120,Human_miRNA_ID_2367980,Human_miRNA_ID_3015765,Human_miRNA_ID_3020103 RMVar_hsa_circ_8254,RMVar_hsa_circ_88421,RMVar_hsa_circ_76121,RMVar_hsa_circ_183960,RMVar_hsa_circ_319430,RMVar_hsa_circ_18257,RMVar_hsa_circ_51759,RMVar_hsa_circ_183962,RMVar_hsa_circ_4430,RMVar_hsa_circ_301395,RMVar_hsa_circ_183961,RMVar_hsa_circ_297899,RMVar_hsa_circ_183963,RMVar_hsa_circ_183964 112752 RMVar_ID_112752 Human_SNP_ID_829582072 m1A Human chr17 + 1679409 1679409 1679409 CACAGGCTGCCCGGCAGGACAATGCTCCCGATACCTGGAAAAATAAGCCCACCAGAGTTTGGCCA CACAGGCTGCCCGGCAGGACAATGCTCCCGATCCCTGGAAAAATAAGCCCACCAGAGTTTGGCCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:1679401..1679425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 tonsil diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 2 head and neck,haematopoietic and lymphoid tissue 112753 RMVar_ID_112753 Human_SNP_ID_829589377 m1A Human chr17 + 4946777 4946777 4946777 TCTGGCCCCCAAGTGTCAGCCCATTCACGTAAAAACTTGACCGGTCTTTGCCAACCAGGACACCC TCTGGCCCCCAAGTGTCAGCCCATTCACGTAACAACTTGACCGGTCTTTGCCAACCAGGACACCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr17:4945726..4946825;chr17:4946726..4946878 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 112754 RMVar_ID_112754 Human_SNP_ID_829594074 m1A Human chr17 + 41905576 41905575 41905576 CATGAGGGAGAGGATAGTCTTGGCATAGTCATAGGTCTGCTGCTCGCTGGGGGCGCCTGAGTACT CATGAGGGAGAGGATAGTCTTGGCATAGTCAT_GGTCTGCTGCTCGCTGGGGGCGCCTGAGTACT TA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:41905478..41905655 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 SKCM 1 - 112755 RMVar_ID_112755 Human_SNP_ID_829600833 m1A Human chr17 - 21000918 21000918 21000918 AGCCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCACGCCAGGCTAATTTTTGTATTTTTAG AGCCTCCCAAGTAGCTGGGACTACAGGCATGCGCCACCACGCCAGGCTAATTTTTGTATTTTTAG T C USP22 Ensembl:ENSG00000124422 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1127815 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_104605,RMVar_hsa_circ_101623,RMVar_hsa_circ_182719,RMVar_hsa_circ_81808,RMVar_hsa_circ_182720,RMVar_hsa_circ_182718 112756 RMVar_ID_112756 Human_SNP_ID_829608579 m1A Human chr17 - 18245075 18245075 18245075 GGAAGAGGAAGGGGCCTCATCCACTGTCTGCTAGCAAAGAATGTACTCAGGTGACACCACCTGCT GGAAGAGGAAGGGGCCTCATCCACTGTCTGCTGGCAAAGAATGTACTCAGGTGACACCACCTGCT T C FLII Ensembl:ENSG00000177731 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:18244901..18245075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck Human_RBP_ID_484537,Human_RBP_ID_4468894,Human_RBP_ID_5114569,Human_RBP_ID_17654606,Human_RBP_ID_22444396,Human_RBP_ID_23209853,Human_RBP_ID_23714401 RMVar_hsa_circ_118444,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_102452,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182464,RMVar_hsa_circ_182465,RMVar_hsa_circ_182463 112757 RMVar_ID_112757 Human_SNP_ID_829617021 m1A Human chr17 - 51120826 51120826 51120826 GCAGCGGCGGTTGGGGTGAGAGCGCCTACGCCACCCCTCCCCTCCTCCGGCCCCGGCCCCCACCC GCAGCGGCGGTTGGGGTGAGAGCGCCTACGCCCCCCCTCCCCTCCTCCGGCCCCGGCCCCCACCC T G SPAG9 Ensembl:ENSG00000008294 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr17:51120726..51120875 26863410 MeRIP-seq:(Medium) rs930281401 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_4465537,Human_RBP_ID_8824838,Human_RBP_ID_9378572,Human_RBP_ID_18419658 RMVar_hsa_circ_266744 112758 RMVar_ID_112758 Human_SNP_ID_829618764 m1A Human chr17 + 81693558 81693558 81693558 CCACCACTGAGCTGCCCCCCGAGTACCTGACCAGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC CCACCACTGAGCTGCCCCCCGAGTACCTGACCGGCCCCCTGTCTCAGCAGTCCCAGGTACTCAGC A G HGS Ensembl:ENSG00000185359 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr17:81693458..81693775;chr17:81693481..81693775 26863196 MeRIP-seq:(Medium) rs762551677 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_904235,Human_RBP_ID_3951364,Human_RBP_ID_5365310,Human_RBP_ID_8466100,Human_RBP_ID_18992830,Human_RBP_ID_19080441,Human_RBP_ID_24373575 Human_Splice_Rec_1881568,Human_Splice_Rec_1881569,Human_Splice_Rec_1881608,Human_Splice_Rec_1881609 Human_miRNA_ID_272329 RMVar_hsa_circ_322769,RMVar_hsa_circ_73768,RMVar_hsa_circ_76901,RMVar_hsa_circ_187728,RMVar_hsa_circ_17845,RMVar_hsa_circ_116462,RMVar_hsa_circ_187730,RMVar_hsa_circ_79730,RMVar_hsa_circ_187731,RMVar_hsa_circ_21404,RMVar_hsa_circ_125517,RMVar_hsa_circ_357759,RMVar_hsa_circ_187733,RMVar_hsa_circ_264841,RMVar_hsa_circ_87300,RMVar_hsa_circ_37666,RMVar_hsa_circ_78502,RMVar_hsa_circ_187736,RMVar_hsa_circ_187737,RMVar_hsa_circ_123553,RMVar_hsa_circ_342586,RMVar_hsa_circ_328249,RMVar_hsa_circ_97811,RMVar_hsa_circ_187738,RMVar_hsa_circ_187739 112759 RMVar_ID_112759 Human_SNP_ID_829622708 m1A Human chr17 - 39218027 39218027 39218027 ACGCCCCCAACCCCACTGCCCCCTCCCTCCCCACCACCCACAGCCTCGGACAGGGGCCTGGCTAC ACGCCCCCAACCCCACTGCCCCCTCCCTCCCCCCCACCCACAGCCTCGGACAGGGGCCTGGCTAC T G STAC2 Ensembl:ENSG00000141750 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:39217148..39218040 26863196 MeRIP-seq:(Medium) rs1221153818 Functional Loss SNV ICGC 33..33 33 STAD 1 - 112760 RMVar_ID_112760 Human_SNP_ID_829628261 m1A Human chr17 + 64504839 64504839 64504839 CCTGCCCTACTTCCTCCAAATCGAGGTGCACCAAACCTGGAATGAAAAAAAACGTTATTCACATT CCTGCCCTACTTCCTCCAAATCGAGGTGCACCGAACCTGGAATGAAAAAAAACGTTATTCACATT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:64504745..64504875 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 112761 RMVar_ID_112761 Human_SNP_ID_829635692 m1A Human chr17 - 64503251 64503250 64503251 CTGAGAAGAACAACCTACCTTGTCCTTGATGAAGCAGATAGAATGCTTGATATGGGCTTTGAACC CTGAGAAGAACAACCTACCTTGTCCTTGATGA_GCAGATAGAATGCTTGATATGGGCTTTGAACC CT C DDX5 Ensembl:ENSG00000108654 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:64503206..64503279 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUSC 1 - Human_RBP_ID_47429,Human_RBP_ID_1540215,Human_RBP_ID_1867008,Human_RBP_ID_2519324,Human_RBP_ID_3534239,Human_RBP_ID_3952818,Human_RBP_ID_9376641,Human_RBP_ID_13130730,Human_RBP_ID_18706145,Human_RBP_ID_22004431,Human_RBP_ID_22500205,Human_RBP_ID_23743534,Human_RBP_ID_24544938,Human_RBP_ID_26330838,Human_RBP_ID_26968879,Human_RBP_ID_27258331,Human_RBP_ID_27813023 Human_Splice_Rec_1855050,Human_Splice_Rec_1855051,Human_Splice_Rec_1855072,Human_Splice_Rec_1855073,Human_Splice_Rec_1855094,Human_Splice_Rec_1855095,Human_Splice_Rec_1855118,Human_Splice_Rec_1855119,Human_Splice_Rec_1855138,Human_Splice_Rec_1855139,Human_Splice_Rec_1855162,Human_Splice_Rec_1855163,Human_Splice_Rec_1855199,Human_Splice_Rec_1855208,Human_Splice_Rec_1855209,Human_Splice_Rec_1855216,Human_Splice_Rec_1855217,Human_Splice_Rec_1855222,Human_Splice_Rec_1855223,Human_Splice_Rec_1855226,Human_Splice_Rec_1855227,Human_Splice_Rec_1855230,Human_Splice_Rec_1855231,Human_Splice_Rec_1855242,Human_Splice_Rec_1855243,Human_Splice_Rec_1855250 Human_miRNA_ID_1953883 RMVar_hsa_circ_51270,RMVar_hsa_circ_13328,RMVar_hsa_circ_59606,RMVar_hsa_circ_60060,RMVar_hsa_circ_108312,RMVar_hsa_circ_320284,RMVar_hsa_circ_291366,RMVar_hsa_circ_97178,RMVar_hsa_circ_186434,RMVar_hsa_circ_186435,RMVar_hsa_circ_186433,RMVar_hsa_circ_186437,RMVar_hsa_circ_82355,RMVar_hsa_circ_362799,RMVar_hsa_circ_363186,RMVar_hsa_circ_95285,RMVar_hsa_circ_186440,RMVar_hsa_circ_57679,RMVar_hsa_circ_310253,RMVar_hsa_circ_186441,RMVar_hsa_circ_320991 112762 RMVar_ID_112762 Human_SNP_ID_829637998 m1A Human chr17 + 42388192 42388191 42388192 TCTCCCGGCCCCACTGCAGCGTCCATCACAACATCCCCAAGGTCCCAGAGGCCCCCTGCCGCTGC TCTCCCGGCCCCACTGCAGCGTCCATCACAAC_TCCCCAAGGTCCCAGAGGCCCCCTGCCGCTGC CA C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr17:42388189..42388475 26863196 MeRIP-seq:(Medium) rs1273865825 Functional Loss DEL ICGC 33..33 33 PBCA 1 - 112763 RMVar_ID_112763 Human_SNP_ID_829642118 m1A Human chr17 - 20204425 20204425 20204425 AGTTGGACTGGACACTGATTTCCTGGGGTTGGAGGGACCACGTGGCACAGACCTCTCTCTTGAGA AGTTGGACTGGACACTGATTTCCTGGGGTTGGGGGGACCACGTGGCACAGACCTCTCTCTTGAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:20204376..20204475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - 112764 RMVar_ID_112764 Human_SNP_ID_829643390 m1A Human chr17 - 68532257 68532257 68532257 ACTCATTTAAGTACATTTTGGCATTTAAACAAAGATCAAATCAAGCTTTAAGCTTGTAAGAACGT ACTCATTTAAGTACATTTTGGCATTTAAACAATGATCAAATCAAGCTTTAAGCTTGTAAGAACGT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:68532123..68532422 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - 112765 RMVar_ID_112765 Human_SNP_ID_829647326 m1A Human chr17 - 51161843 51161843 51161843 ATGTGAAAAGCAATGTGGTCTGCCCTCCTGTCATTCATAGATCCAGTTCTGAGCACAGCTCGTGT ATGTGAAAAGCAATGTGGTCTGCCCTCCTGTCGTTCATAGATCCAGTTCTGAGCACAGCTCGTGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:51161793..51161980 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus 112766 RMVar_ID_112766 Human_SNP_ID_829648865 m1A Human chr17 - 50719659 50719659 50719659 CGCCAACGAAAACACGGGCGACACCGTCGCCAATCTCCTCGGCCCGCTCTCAGGCCGAAATCCCT CGCCAACGAAAACACGGGCGACACCGTCGCCAGTCTCCTCGGCCCGCTCTCAGGCCGAAATCCCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr17:50719593..50722724;chr17:50719601..50719936;chr17:50719576..50722724;chr17:50719576..50719850 26863196 MeRIP-seq:(Medium) rs953784011 Functional Loss SNV ICGC 33..33 33 MELA 1 - 112767 RMVar_ID_112767 Human_SNP_ID_829653918 m1A Human chr17 + 80104878 80104878 80104878 ACAGCCGCTTCGATTGCGCCCCTGACAAGGCCATCACCCAGGAACAGTGCGAGGCCCGCGGCTGT ACAGCCGCTTCGATTGCGCCCCTGACAAGGCCTTCACCCAGGAACAGTGCGAGGCCCGCGGCTGT A T GAA Ensembl:ENSG00000171298 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:80104742..80104881 26863196 MeRIP-seq:(Medium) rs745963730 Functional Loss SNV COSMIC 33..33 33 lung bronchioloalveolar_adenocarcinoma 2 lung Human_RBP_ID_26973283 RMVar_hsa_circ_9198 112768 RMVar_ID_112768 Human_SNP_ID_829663851 m1A Human chr17 - 58205577 58205577 58205577 CTCATTCTACTGCTTGGGGCTTGCTGAGGTTGAGATATGAGTTATTTCTGAGTAAGTGAAGGCTG CTCATTCTACTGCTTGGGGCTTGCTGAGGTTGGGATATGAGTTATTTCTGAGTAAGTGAAGGCTG T C MKS1 Ensembl:ENSG00000011143 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:58205528..58205615 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THYM 1 - Human_RBP_ID_6620181,Human_RBP_ID_13094347 RMVar_hsa_circ_108112,RMVar_hsa_circ_109051,RMVar_hsa_circ_185625,RMVar_hsa_circ_99537,RMVar_hsa_circ_185626,RMVar_hsa_circ_185624 112769 RMVar_ID_112769 Human_SNP_ID_829665117 m1A Human chr17 + 63049795 63049795 63049795 GCTGGGATGGAAGCAGAGAAACCAGGTTAGTCATGAGGGTGGCTGGGACTCAGGGTGGTGGTAGC GCTGGGATGGAAGCAGAGAAACCAGGTTAGTCGTGAGGGTGGCTGGGACTCAGGGTGGTGGTAGC A G TANC2 Ensembl:ENSG00000170921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63049771..63049921 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_6631377 RMVar_hsa_circ_186253,RMVar_hsa_circ_36550,RMVar_hsa_circ_119468,RMVar_hsa_circ_306450,RMVar_hsa_circ_281653,RMVar_hsa_circ_37006,RMVar_hsa_circ_186254,RMVar_hsa_circ_186256,RMVar_hsa_circ_84303,RMVar_hsa_circ_186255 112770 RMVar_ID_112770 Human_SNP_ID_829674503 m1A Human chr17 - 53757473 53757473 53757473 CAGGTTCAAGGCGTTTGTTGCTATCGGGGACTACAATGGCCACGTCGGCCTGGGTGTTAAGTGCT CAGGTTCAAGGCGTTTGTTGCTATCGGGGACTGCAATGGCCACGTCGGCCTGGGTGTTAAGTGCT T C RPS2P48,AC034268.2 Ensembl:ENSG00000233380,Ensembl:ENSG00000285939 Pseudogene,lincRNA exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:53757345..53757472 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_493910,Human_RBP_ID_9073629,Human_RBP_ID_17378927,Human_RBP_ID_23735307 Human_miRNA_ID_1855357 112771 RMVar_ID_112771 Human_SNP_ID_829675739 m1A Human chr17 - 47971349 47971349 47971349 ATGGGCACGTGCTGATGGTCCTGGCGGGAAACACGGTGAGGAGGGGGGCGTGAGCGCGGAGAGAG ATGGGCACGTGCTGATGGTCCTGGCGGGAAACTCGGTGAGGAGGGGGGCGTGAGCGCGGAGAGAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:47971345..47971450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 DLBC,MELA 2 - 112772 RMVar_ID_112772 Human_SNP_ID_829677531 m1A Human chr17 - 58005575 58005575 58005575 CCAATAGGGAGAAACTGCCTACATCCGGGTTAAAGTTGATGGGCCCAGAAGTCCAAGTTATGGAA CCAATAGGGAGAAACTGCCTACATCCGGGTTACAGTTGATGGGCCCAGAAGTCCAAGTTATGGAA T G AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:58005352..58005625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_48258,Human_RBP_ID_495285,Human_RBP_ID_820697,Human_RBP_ID_902540,Human_RBP_ID_1009499,Human_RBP_ID_1369118,Human_RBP_ID_1538241,Human_RBP_ID_1864018,Human_RBP_ID_3530009,Human_RBP_ID_8458200,Human_RBP_ID_9376438,Human_RBP_ID_9870353,Human_RBP_ID_13093513,Human_RBP_ID_17492683,Human_RBP_ID_17897072,Human_RBP_ID_18179084,Human_RBP_ID_18703689,Human_RBP_ID_22500006,Human_RBP_ID_22805856,Human_RBP_ID_22954859,Human_RBP_ID_23738235,Human_RBP_ID_24545225,Human_RBP_ID_25304897,Human_RBP_ID_26967241,Human_RBP_ID_27667499 Human_Splice_Rec_1844748,Human_Splice_Rec_1844758,Human_Splice_Rec_1844774,Human_Splice_Rec_1844786 Human_miRNA_ID_2892333 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616,RMVar_hsa_circ_185618,RMVar_hsa_circ_342076 112773 RMVar_ID_112773 Human_SNP_ID_829679894 m1A Human chr17 - 38717915 38717915 38717915 GGCTGCTCTCAGCTTGGGAGAGGAGGGGATTAACGGCACCCATGGGGGTTCCAAAGATGTGGGTA GGCTGCTCTCAGCTTGGGAGAGGAGGGGATTACCGGCACCCATGGGGGTTCCAAAGATGTGGGTA T G AC006449.3 Ensembl:ENSG00000275665 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38717821..38717981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 112774 RMVar_ID_112774 Human_SNP_ID_829694778 m1A Human chr17 + 81104089 81104088 81104089 AACACACTCCCCGTGCGCAAGAGCGTGACCCCAAAAAACAGCTATGCCACCAGTAAGGGCTCCGC AACACACTCCCCGTGCGCAAGAGCGTGACCCC_AAAAACAGCTATGCCACCAGTAAGGGCTCCGC CA C BAIAP2 Ensembl:ENSG00000175866 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:81104018..81104165 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 CHOL 1 - Human_RBP_ID_26814097 Human_Splice_Rec_1879615,Human_Splice_Rec_1879675,Human_Splice_Rec_1879701,Human_Splice_Rec_1879727,Human_Splice_Rec_1879753,Human_Splice_Rec_1879781,Human_Splice_Rec_1879809,Human_Splice_Rec_1879957,Human_Splice_Rec_1879983,Human_Splice_Rec_1879991,Human_Splice_Rec_1879999 RMVar_hsa_circ_12563,RMVar_hsa_circ_23177,RMVar_hsa_circ_348672,RMVar_hsa_circ_65124,RMVar_hsa_circ_66655,RMVar_hsa_circ_32036 112775 RMVar_ID_112775 Human_SNP_ID_829701192 m1A Human chr17 - 17206063 17206063 17206063 GCTCCCCGAGGGCTGCCCGTGCGGCCTGCCCCACGGCGAGAGCGCGCTAAGCCGCCTGCTGCGTG GCTCCCCGAGGGCTGCCCGTGCGGCCTGCCCCCCGGCGAGAGCGCGCTAAGCCGCCTGCTGCGTG T G PLD6,AC055811.2 Ensembl:ENSG00000179598,Ensembl:ENSG00000264187 Protein coding,Protein coding CDS,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:17206019..17206383 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 112776 RMVar_ID_112776 Human_SNP_ID_829703132 m1A Human chr17 - 40417822 40417815 40417822 TCTCGTGGGGTCCTGCCTGTTTAGTCGCTTTCAGGGTTCTTGAGCCCCTTCACGACCGTCACCAT TCTCGTGGGGTCCTGCCTGTTTAGTCGCTTTC_______TTGAGCCCCTTCACGACCGTCACCAT AGAACCCT A TOP2A Ensembl:ENSG00000131747 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:40417751..40417900 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..39 33 LUAD 1 - Human_RBP_ID_50592,Human_RBP_ID_133380,Human_RBP_ID_1857766,Human_RBP_ID_2505805,Human_RBP_ID_3522835,Human_RBP_ID_4465361,Human_RBP_ID_8817679,Human_RBP_ID_9071856,Human_RBP_ID_9257855,Human_RBP_ID_9289057,Human_RBP_ID_9326613,Human_RBP_ID_18697316,Human_RBP_ID_23118888,Human_RBP_ID_26960541,Human_RBP_ID_27665028 Human_Splice_Rec_1814523 112777 RMVar_ID_112777 Human_SNP_ID_829710076 m1A Human chr17 + 38753246 38753246 38753246 CTGCAGACAGGCGCTTCGGGATCCAGGCCCAGATGGTGACCACGGACTTCCAGAAGATCTTTCCC CTGCAGACAGGCGCTTCGGGATCCAGGCCCAGTTGGTGACCACGGACTTCCAGAAGATCTTTCCC A T PSMB3 Ensembl:ENSG00000277791 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:38753196..38753271 26863196 MeRIP-seq:(Medium) rs4907 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_488098,Human_RBP_ID_1532812,Human_RBP_ID_1856698,Human_RBP_ID_4422803,Human_RBP_ID_12989714,Human_RBP_ID_18696176 Human_Splice_Rec_1810002,Human_Splice_Rec_1810003,Human_Splice_Rec_1810012,Human_Splice_Rec_1810013,Human_Splice_Rec_1810018,Human_Splice_Rec_1810019,Human_Splice_Rec_1810028,Human_Splice_Rec_1810029 RMVar_hsa_circ_88325,RMVar_hsa_circ_110436,RMVar_hsa_circ_183817,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819 112778 RMVar_ID_112778 Human_SNP_ID_829710789 m1A Human chr17 + 45149245 45149245 45149245 AATATCAACACCAGCCTCAAACTAGCAACTGTACAGGTGCTGCTGCTGTCCAGGAAGAGCTGAAC AATATCAACACCAGCCTCAAACTAGCAACTGTCCAGGTGCTGCTGCTGTCCAGGAAGAGCTGAAC A C HEXIM1 Ensembl:ENSG00000186834 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:45149195..45149383 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 2 kidney Human_RBP_ID_50971,Human_RBP_ID_1859786,Human_RBP_ID_4432553,Human_RBP_ID_5525640,Human_RBP_ID_6600936,Human_RBP_ID_18699628,Human_RBP_ID_26963209 112779 RMVar_ID_112779 Human_SNP_ID_829711341 m1A Human chr17 - 799967 799967 799967 GGATTACAGGCACCCGCCACCGTACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCAC GGATTACAGGCACCCGCCACCGTACCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCAC T C NXN Ensembl:ENSG00000167693 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs538435 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,liver hepatocellular_carcinoma 5 liver 112780 RMVar_ID_112780 Human_SNP_ID_829713681 m1A Human chr17 - 76007086 76007086 76007086 GCGCTCCCTTCGCTGACACGGGCCAAGGAGCCAGTGGGGAAGTGCGTGTGTTGGGCCAGGTAGGA GCGCTCCCTTCGCTGACACGGGCCAAGGAGCCGGTGGGGAAGTGCGTGTGTTGGGCCAGGTAGGA T C EVPL Ensembl:ENSG00000167880 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:76007060..76007197 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5525864 Human_Splice_Rec_1870323 RMVar_hsa_circ_118197,RMVar_hsa_circ_124288,RMVar_hsa_circ_119593,RMVar_hsa_circ_187149,RMVar_hsa_circ_94567,RMVar_hsa_circ_103978,RMVar_hsa_circ_187151,RMVar_hsa_circ_88770,RMVar_hsa_circ_187150,RMVar_hsa_circ_187147,RMVar_hsa_circ_187148,RMVar_hsa_circ_187146 112781 RMVar_ID_112781 Human_SNP_ID_829715913 m1A Human chr17 - 59079802 59079802 59079802 TTCGGGAAATTAGGAATGCAGTGGAGATGATGATTGCACGGTTAGACACACAGCTGAAGAATAAG TTCGGGAAATTAGGAATGCAGTGGAGATGATGCTTGCACGGTTAGACACACAGCTGAAGAATAAG T G TRIM37 Ensembl:ENSG00000108395 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:59075682..59081140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_RBP_ID_47209,Human_RBP_ID_1864491,Human_RBP_ID_3950905,Human_RBP_ID_9376465,Human_RBP_ID_13099923,Human_RBP_ID_23739125 Human_Splice_Rec_1846708,Human_Splice_Rec_1846709,Human_Splice_Rec_1846758,Human_Splice_Rec_1846759,Human_Splice_Rec_1846802,Human_Splice_Rec_1846803,Human_Splice_Rec_1846846,Human_Splice_Rec_1846847,Human_Splice_Rec_1846882,Human_Splice_Rec_1846883,Human_Splice_Rec_1846895,Human_Splice_Rec_1846906,Human_Splice_Rec_1846907,Human_Splice_Rec_1846918 RMVar_hsa_circ_313386,RMVar_hsa_circ_2033,RMVar_hsa_circ_185682,RMVar_hsa_circ_33718,RMVar_hsa_circ_284542,RMVar_hsa_circ_375375,RMVar_hsa_circ_98405,RMVar_hsa_circ_185696,RMVar_hsa_circ_185698,RMVar_hsa_circ_185699,RMVar_hsa_circ_185697,RMVar_hsa_circ_106105,RMVar_hsa_circ_185709,RMVar_hsa_circ_185703,RMVar_hsa_circ_371211,RMVar_hsa_circ_335074,RMVar_hsa_circ_350749,RMVar_hsa_circ_185708,RMVar_hsa_circ_278743,RMVar_hsa_circ_185710,RMVar_hsa_circ_331248,RMVar_hsa_circ_185719,RMVar_hsa_circ_376690,RMVar_hsa_circ_52843,RMVar_hsa_circ_185725,RMVar_hsa_circ_185726,RMVar_hsa_circ_349656,RMVar_hsa_circ_376507,RMVar_hsa_circ_303374,RMVar_hsa_circ_284967,RMVar_hsa_circ_25861,RMVar_hsa_circ_36607,RMVar_hsa_circ_103840,RMVar_hsa_circ_185727,RMVar_hsa_circ_185728,RMVar_hsa_circ_315596,RMVar_hsa_circ_310430,RMVar_hsa_circ_288790,RMVar_hsa_circ_185734,RMVar_hsa_circ_291329,RMVar_hsa_circ_313544,RMVar_hsa_circ_185735,RMVar_hsa_circ_287279,RMVar_hsa_circ_41403,RMVar_hsa_circ_41589,RMVar_hsa_circ_185739,RMVar_hsa_circ_185740,RMVar_hsa_circ_185738,RMVar_hsa_circ_301787,RMVar_hsa_circ_323884,RMVar_hsa_circ_314935,RMVar_hsa_circ_288278,RMVar_hsa_circ_17756,RMVar_hsa_circ_185741,RMVar_hsa_circ_185743,RMVar_hsa_circ_185744,RMVar_hsa_circ_185742,RMVar_hsa_circ_289353,RMVar_hsa_circ_22630,RMVar_hsa_circ_348968,RMVar_hsa_circ_349303,RMVar_hsa_circ_73368,RMVar_hsa_circ_314749,RMVar_hsa_circ_325782,RMVar_hsa_circ_341307,RMVar_hsa_circ_316664,RMVar_hsa_circ_293644,RMVar_hsa_circ_185747,RMVar_hsa_circ_185748,RMVar_hsa_circ_276846,RMVar_hsa_circ_337675,RMVar_hsa_circ_265955,RMVar_hsa_circ_185749,RMVar_hsa_circ_185750 112782 RMVar_ID_112782 Human_SNP_ID_829715986 m1A Human chr17 + 28893052 28893050 28893053 AAGGGCAACATTGCCAGGTTCCCAAGGGTAGCAACAACAGGAAGCTGAAACTGCCAGATTACCCG AAGGGCAACATTGCCAGGTTCCCAAGGGTAG___CAACAGGAAGCTGAAACTGCCAGATTACCCG GCAA G AC024267.4 Ensembl:ENSG00000264304 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:28893050..28893403 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 CHOL 1 - 112783 RMVar_ID_112783 Human_SNP_ID_829724877 m1A Human chr17 + 65056493 65056493 65056493 CATAGGTCTTTTCCCGAGACAGGCATTTGTCGATCTCCTTGGACTTGCGTTGCTGCTCGGCCTCG CATAGGTCTTTTCCCGAGACAGGCATTTGTCGGTCTCCTTGGACTTGCGTTGCTGCTCGGCCTCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:65056442..65056641 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 4 haematopoietic and lymphoid tissue 112784 RMVar_ID_112784 Human_SNP_ID_829726275 m1A Human chr17 + 7675209 7675208 7675209 CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGCAAAACATCTTGTTGAGGGCAGGGGAGTACTGTA CAGCTGCACAGGGCAGGTCTTGGCCAGTTGGC_AAACATCTTGTTGAGGGCAGGGGAGTACTGTA CA C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr17:7675158..7675284 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 STAD,HNSC 3 - 112785 RMVar_ID_112785 Human_SNP_ID_829726982 m1A Human chr17 - 76726523 76726523 76726523 CCAGGCCGGGGAGGGGTGCGTTAGTGTCAGGAAGCGGGCTGCGCCGAGGTCGTAGCGGAACCAGC CCAGGCCGGGGAGGGGTGCGTTAGTGTCAGGAGGCGGGCTGCGCCGAGGTCGTAGCGGAACCAGC T C JMJD6 Ensembl:ENSG00000070495 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:76725526..76726700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_500726,Human_RBP_ID_4465717,Human_RBP_ID_5467058,Human_RBP_ID_18419740,Human_RBP_ID_22063356 112786 RMVar_ID_112786 Human_SNP_ID_829727127 m1A Human chr17 - 75876428 75876428 75876428 CCGGCTGTTTGCAGATGCTGCGGCCGCCCTGCAGGGCTTCCAGACCCAGGTGCTGGGCTTCATCG CCGGCTGTTTGCAGATGCTGCGGCCGCCCTGCGGGGCTTCCAGACCCAGGTGCTGGGCTTCATCG T C TRIM47 Ensembl:ENSG00000132481 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr17:75876243..75876521;chr17:75876081..75876543 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4466813,Human_RBP_ID_22444966 Human_Splice_Rec_1869498,Human_Splice_Rec_1869508,Human_Splice_Rec_1869522 RMVar_hsa_circ_36413 112787 RMVar_ID_112787 Human_SNP_ID_829732481 m1A Human chr17 - 18246961 18246961 18246961 GGAGGGCAAGAAGTTTGCGCGGCTGCCGGAAGAGGAGTTTGGCCACTTCTACACGCAGGACTGCT GGAGGGCAAGAAGTTTGCGCGGCTGCCGGAAGCGGAGTTTGGCCACTTCTACACGCAGGACTGCT T G FLII Ensembl:ENSG00000177731 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:18246901..18246975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_8824463 Human_Splice_Rec_1787598,Human_Splice_Rec_1787599,Human_Splice_Rec_1787698,Human_Splice_Rec_1787699,Human_Splice_Rec_1787756,Human_Splice_Rec_1787757,Human_Splice_Rec_1787814,Human_Splice_Rec_1787815,Human_Splice_Rec_1787879,Human_Splice_Rec_1787886,Human_Splice_Rec_1787887 Human_miRNA_ID_878046 RMVar_hsa_circ_76013,RMVar_hsa_circ_127732,RMVar_hsa_circ_120191,RMVar_hsa_circ_182466,RMVar_hsa_circ_112879,RMVar_hsa_circ_182468,RMVar_hsa_circ_85370,RMVar_hsa_circ_182467,RMVar_hsa_circ_182465,RMVar_hsa_circ_1907,RMVar_hsa_circ_92117,RMVar_hsa_circ_182469,RMVar_hsa_circ_182470 112788 RMVar_ID_112788 Human_SNP_ID_829736736 m1A Human chr17 - 43339138 43339138 43339138 ATGGTGAGAAGTGACAAGAAGACAAGAGTGTGAGCCTTTTGTTATGCCCAGGCAGGGCCACCAGA ATGGTGAGAAGTGACAAGAAGACAAGAGTGTGGGCCTTTTGTTATGCCCAGGCAGGGCCACCAGA T C LINC00910 Ensembl:ENSG00000188825 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:43339089..43339160 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112789 RMVar_ID_112789 Human_SNP_ID_829738280 m1A Human chr17 - 82939475 82939475 82939475 AGGTGGCCGTGCAGGAAGGGCCTTCACTCACCACGCAGTGTCACTGAGCACAGTCACCACCTCGT AGGTGGCCGTGCAGGAAGGGCCTTCACTCACCGCGCAGTGTCACTGAGCACAGTCACCACCTCGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:82939428..82939501 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung 112790 RMVar_ID_112790 Human_SNP_ID_829739706 m1A Human chr17 - 51260716 51260716 51260716 CTCGGCCGGGCCGGCGGTTTCCGCTGGGATGAAGGGGCAGGCTTTTGGGGAGGCCCGCCTGGCCC CTCGGCCGGGCCGGCGGTTTCCGCTGGGATGAGGGGGCAGGCTTTTGGGGAGGCCCGCCTGGCCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr17:51260576..51260726 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112791 RMVar_ID_112791 Human_SNP_ID_829751203 m1A Human chr17 + 1684733 1684733 1684733 GCCCGGCCTAACCCCTTCGGTCACTCGGCCCGACCCGACCACGCCTCCCGCAGCCCGGCCTTAAA GCCCGGCCTAACCCCTTCGGTCACTCGGCCCGGCCCGACCACGCCTCCCGCAGCCCGGCCTTAAA A G AC130343.2 Ensembl:ENSG00000277597 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr17:1684725..1684850 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112792 RMVar_ID_112792 Human_SNP_ID_829752049 m1A Human chr17 + 1491462 1491462 1491462 CGCCTCCGGGTCGTGGGACCCCCCCCCCCCGCACGGGTCCACGCGGCCGTTCTTCGGCCCCAGCG CGCCTCCGGGTCGTGGGACCCCCCCCCCCCGCCCGGGTCCACGCGGCCGTTCTTCGGCCCCAGCG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:1491458..1491675 26863196 MeRIP-seq:(Medium) rs1212680395 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 112793 RMVar_ID_112793 Human_SNP_ID_829753385 m1A Human chr17 - 9575731 9575731 9575731 TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGAGAGCAGGCAATCACTTCGCATTGCCGCTGGTG TGGAGGGACCTTCGGGGAGGCCGGGCTTCCGGGGAGCAGGCAATCACTTCGCATTGCCGCTGGTG T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr17:9575716..9575805 26863196 MeRIP-seq:(Medium) rs7210038 Functional Loss SNV ICGC 33..33 33 COCA 5 - RMVar_hsa_circ_118911,RMVar_hsa_circ_182093 112794 RMVar_ID_112794 Human_SNP_ID_829759619 m1A Human chr17 + 7229871 7229871 7229871 CCAGGCTGGTACTCTCCAGCTCGCTGGTCATGAGGGTAGAGGAGCTCTCGTATCCGGCCAGGTGG CCAGGCTGGTACTCTCCAGCTCGCTGGTCATGGGGGTAGAGGAGCTCTCGTATCCGGCCAGGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:7229820..7229921 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver 112795 RMVar_ID_112795 Human_SNP_ID_829771705 m1A Human chr17 + 38760555 38760555 38760555 CCATGGTGACTGATGACTTTGTGGTCAGTGGCACCTGCGCCGAACAAATGTACGGAATGTGTGAG CCATGGTGACTGATGACTTTGTGGTCAGTGGCGCCTGCGCCGAACAAATGTACGGAATGTGTGAG A G PSMB3 Ensembl:ENSG00000277791 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38760435..38760646 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 4 - Human_RBP_ID_488108,Human_RBP_ID_1532819,Human_RBP_ID_1856703,Human_RBP_ID_3521698,Human_RBP_ID_22442894,Human_RBP_ID_22760763,Human_RBP_ID_23723865,Human_RBP_ID_27451496,Human_RBP_ID_27560968 Human_Splice_Rec_1810007,Human_Splice_Rec_1810022,Human_Splice_Rec_1810023,Human_Splice_Rec_1810035 Human_miRNA_ID_2533450 RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819,RMVar_hsa_circ_183820,RMVar_hsa_circ_95821,RMVar_hsa_circ_126364,RMVar_hsa_circ_361380,RMVar_hsa_circ_183822 112796 RMVar_ID_112796 Human_SNP_ID_829779266 m1A Human chr17 + 80468124 80468124 80468124 ATCAGATTAAGGAGTAAATGGGAACTACGTGGATTAGATTTGCGGCTGTGTCATCGACCTTTCTC ATCAGATTAAGGAGTAAATGGGAACTACGTGGGTTAGATTTGCGGCTGTGTCATCGACCTTTCTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr17:80468073..80468239 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112797 RMVar_ID_112797 Human_SNP_ID_829783284 m1A Human chr17 - 58007105 58007105 58007105 ATGTCGGGAGGTGGTGTGATTCGTGGCCCCGCAGGGAACAACGATTGCCGCATCTACGTGGGTAA ATGTCGGGAGGTGGTGTGATTCGTGGCCCCGCGGGGAACAACGATTGCCGCATCTACGTGGGTAA T C AC015813.2,SRSF1 Ensembl:ENSG00000266086,Ensembl:ENSG00000136450 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr17:58007060..58007275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_236262,Human_RBP_ID_495298,Human_RBP_ID_765369,Human_RBP_ID_1009510,Human_RBP_ID_1538264,Human_RBP_ID_1864029,Human_RBP_ID_3530020,Human_RBP_ID_4441189,Human_RBP_ID_6619719,Human_RBP_ID_8820277,Human_RBP_ID_9074147,Human_RBP_ID_18419670,Human_RBP_ID_18703717,Human_RBP_ID_22061541,Human_RBP_ID_22805882,Human_RBP_ID_23129486,Human_RBP_ID_23738262,Human_RBP_ID_27838489 Human_miRNA_ID_2959403,Human_miRNA_ID_3066269 RMVar_hsa_circ_76095,RMVar_hsa_circ_185616 112798 RMVar_ID_112798 Human_SNP_ID_829783866 m1A Human chr17 + 10695700 10695700 10695700 AACAACAAAAAAGGTGCTAGTCCATAGCCAGGAAGACCTTTATACAGGGCTGAGCAGATGATAAT AACAACAAAAAAGGTGCTAGTCCATAGCCAGGGAGACCTTTATACAGGGCTGAGCAGATGATAAT A G lnc-ADPRM-6 RNACentral:URS0000D5D6C5 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:10695696..10695771 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 112799 RMVar_ID_112799 Human_SNP_ID_829789612 m1A Human chr17 - 38726380 38726354 38726380 AGGCAGACAGACACACACACACACACACACACACACACACATGCACGCACACACACACTCACACA AGGCAGACAGACACACACACACACACACACAC__________________________TCACACA AGTGTGTGTGTGCGTGCATGTGTGTGT A lnc-PCGF2-3 RNACentral:URS00008B5F13 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr17:38726329..38726485 26863196 MeRIP-seq:(Medium) rs1452089768 Functional Loss DEL TCGA 33..58 33 BRCA 1 - 112800 RMVar_ID_112800 Human_SNP_ID_829794115 m1A Human chr17 + 5024255 5024255 5024255 TCCCCAGAAGTGCTGGGGCAGGGAGGCCCAGGAGATGAGAGAGAAGGTCCGAGTAGGTGATAGAA TCCCCAGAAGTGCTGGGGCAGGGAGGCCCAGGGGATGAGAGAGAAGGTCCGAGTAGGTGATAGAA A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr17:5024226..5024300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4438933,Human_RBP_ID_5114494,Human_RBP_ID_6613343,Human_RBP_ID_13072685,Human_RBP_ID_17895989,Human_RBP_ID_22761276,Human_RBP_ID_24552228 Human_miRNA_ID_254166,Human_miRNA_ID_2041023,Human_miRNA_ID_3020007,Human_miRNA_ID_3118618 RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_181583,RMVar_hsa_circ_75706,RMVar_hsa_circ_119211,RMVar_hsa_circ_181585,RMVar_hsa_circ_86680,RMVar_hsa_circ_181586,RMVar_hsa_circ_181587 112801 RMVar_ID_112801 Human_SNP_ID_829795169 m1A Human chr17 - 75405514 75405514 75405514 GCCGCTCGCAGCGTTGTGGAGGGGCGGGCCGGACGCTGAGCGGAGCAGCTGCGCCACGGTGAGTA GCCGCTCGCAGCGTTGTGGAGGGGCGGGCCGGGCGCTGAGCGGAGCAGCTGCGCCACGGTGAGTA T C GRB2 Ensembl:ENSG00000177885 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr17:75405501..75405525 32194978 MeRIP-seq:(Medium) rs982834508 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_238198,Human_RBP_ID_4464781,Human_RBP_ID_5237932,Human_RBP_ID_5420489,Human_RBP_ID_5466990,Human_RBP_ID_8463006,Human_RBP_ID_8824949,Human_RBP_ID_8941848,Human_RBP_ID_9289358,Human_RBP_ID_9327433,Human_RBP_ID_9353451,Human_RBP_ID_22061633,Human_RBP_ID_22443896,Human_RBP_ID_24552523 Human_Splice_Rec_1865787,Human_Splice_Rec_1865797,Human_Splice_Rec_1865805,Human_Splice_Rec_1865839 112802 RMVar_ID_112802 Human_SNP_ID_829816836 m1A Human chr17 - 7002305 7002305 7002305 TTACCATGCTAACATACATCTCTATCCACCTTACTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG TTACCATGCTAACATACATCTCTATCCACCTTGCTGTTGGGCAGGTATGAGCGGCTTGCTGGCTG T C AC040977.2,ALOX12-AS1 Ensembl:ENSG00000267047,Ensembl:ENSG00000215067 lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13396 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_20263410 GWAS_ID_13566,GWAS_ID_13567,GWAS_ID_13568,GWAS_ID_13569,GWAS_ID_13570,GWAS_ID_13571,GWAS_ID_13572,GWAS_ID_13573,GWAS_ID_13574,GWAS_ID_13575,GWAS_ID_13576,GWAS_ID_13577,GWAS_ID_13578,GWAS_ID_13579,GWAS_ID_13580,GWAS_ID_13581,GWAS_ID_13582,GWAS_ID_13583,GWAS_ID_13584,GWAS_ID_13585,GWAS_ID_13586,GWAS_ID_13587,GWAS_ID_13588,GWAS_ID_13589,GWAS_ID_13590,GWAS_ID_13591 112803 RMVar_ID_112803 Human_SNP_ID_829817053 m1A Human chr17 - 63832238 63832238 63832238 GGACACTCCAGTTCTCTAGCATGGCCTGAGGTATGGGGTATGTGCATGTGGAGGCCAGGGTAAGG GGACACTCCAGTTCTCTAGCATGGCCTGAGGTGTGGGGTATGTGCATGTGGAGGCCAGGGTAAGG T C SMARCD2 Ensembl:ENSG00000108604 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr17:63832126..63832300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_497134,Human_RBP_ID_1009972,Human_RBP_ID_4445221,Human_RBP_ID_6633005,Human_RBP_ID_9353331,Human_RBP_ID_13129470,Human_RBP_ID_17905095,Human_RBP_ID_18295516,Human_RBP_ID_21975652,Human_RBP_ID_22475697 Human_miRNA_ID_3092109 RMVar_hsa_circ_119009,RMVar_hsa_circ_112820,RMVar_hsa_circ_115597,RMVar_hsa_circ_186384,RMVar_hsa_circ_186386,RMVar_hsa_circ_75712,RMVar_hsa_circ_186385,RMVar_hsa_circ_186383 112804 RMVar_ID_112804 Human_SNP_ID_825524524 m1A Human chr16 + 30736593 30736593 30736593 TGCCATGAAATTCCTGGAGGCCTCACTGGAGGAGGTGAGCCGAGAGGAGCTCAAACAGGCAGAAG TGCCATGAAATTCCTGGAGGCCTCACTGGAGGGGGTGAGCCGAGAGGAGCTCAAACAGGCAGAAG A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30736347..30736594 32194978 MeRIP-seq:(Medium) rs1028295006 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_816153,Human_RBP_ID_5465716,Human_RBP_ID_5524375,Human_RBP_ID_6508352,Human_RBP_ID_8083152,Human_RBP_ID_8807151,Human_RBP_ID_9286260,Human_RBP_ID_18677903,Human_RBP_ID_18986079,Human_RBP_ID_22200757,Human_RBP_ID_22944848 Human_Splice_Rec_1703726,Human_Splice_Rec_1703727,Human_Splice_Rec_1703782,Human_Splice_Rec_1703783,Human_Splice_Rec_1703874,Human_Splice_Rec_1703875 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_63796,RMVar_hsa_circ_42150,RMVar_hsa_circ_360349,RMVar_hsa_circ_105032,RMVar_hsa_circ_21056,RMVar_hsa_circ_177962 112805 RMVar_ID_112805 Human_SNP_ID_825528359 m1A Human chr16 + 2239940 2239940 2239940 AATACCTTGTTTAAGACCTCCCTGGGACCCACAGGGGCACGTGTGGCCGTAAGCCTGTGGCAGCC AATACCTTGTTTAAGACCTCCCTGGGACCCACGGGGGCACGTGTGGCCGTAAGCCTGTGGCAGCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2239842..2239942 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_12690479 112806 RMVar_ID_112806 Human_SNP_ID_825533118 m1A Human chr16 + 15596803 15596803 15596803 TTCCACGGGGTCCTTGCTGAGCAGTGACTCGGAGGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA TTCCACGGGGTCCTTGCTGAGCAGTGACTCGGCGGTTTCCGAGGAGGGGCAGGGAGGCACGGGGA A C BMERB1 Ensembl:ENSG00000166780 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15596752..15596841 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 112807 RMVar_ID_112807 Human_SNP_ID_825539732 m1A Human chr16 + 72008783 72008783 72008783 ATGACGGAAGGAGCATGGCGTGGAGACACCTGAAAGTGAGTCCCGCGAGTGAGCAGTGTGGATGG ATGACGGAAGGAGCATGGCGTGGAGACACCTGCAAGTGAGTCCCGCGAGTGAGCAGTGTGGATGG A C DHODH Ensembl:ENSG00000102967 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:72008774..72008910 26863196 MeRIP-seq:(Medium) rs3213422 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 7 head and neck Human_RBP_ID_19075108 Human_Splice_Rec_1738347,Human_Splice_Rec_1738361,Human_Splice_Rec_1738375,Human_Splice_Rec_1738383 Clinvar_Rec_528 GWAS_ID_12129,GWAS_ID_12130,GWAS_ID_12131,GWAS_ID_12132,GWAS_ID_12133,GWAS_ID_12134,GWAS_ID_12135,GWAS_ID_12136,GWAS_ID_12137,GWAS_ID_12138,GWAS_ID_12139,GWAS_ID_12140,GWAS_ID_12141,GWAS_ID_12142,GWAS_ID_12143,GWAS_ID_12144,GWAS_ID_12145,GWAS_ID_12146,GWAS_ID_12147,GWAS_ID_12148,GWAS_ID_12149,GWAS_ID_12150,GWAS_ID_12151,GWAS_ID_12152,GWAS_ID_12153,GWAS_ID_12154,GWAS_ID_12155,GWAS_ID_12156,GWAS_ID_12157,GWAS_ID_12158,GWAS_ID_12159,GWAS_ID_12160,GWAS_ID_12161,GWAS_ID_12162,GWAS_ID_12163,GWAS_ID_12164,GWAS_ID_12165,GWAS_ID_12166,GWAS_ID_12167 112808 RMVar_ID_112808 Human_SNP_ID_825541635 m1A Human chr16 - 1975359 1975359 1975359 AGCTGGGACACTGGCTCCTCTGGCAACAGCACAGCAGCCTCCACGCTCTGGAGACGAATTGGGTC AGCTGGGACACTGGCTCCTCTGGCAACAGCACCGCAGCCTCCACGCTCTGGAGACGAATTGGGTC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1975351..1975425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 112809 RMVar_ID_112809 Human_SNP_ID_825541923 m1A Human chr16 - 647532 647532 647532 CCTCTGGCCCCGCTCGCTACCTTCGGACACAAAGCGGACATTCTCCTCGTGGGCCACTGTGTAGG CCTCTGGCCCCGCTCGCTACCTTCGGACACAATGCGGACATTCTCCTCGTGGGCCACTGTGTAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:647393..647575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 112810 RMVar_ID_112810 Human_SNP_ID_825546841 m1A Human chr16 + 72959644 72959644 72959644 CCCCGCGCCAGGGAGAGAGTTCAGGAAAAGCGAGGGGAGAGGCCCACTGCCACTGCCACTCCCAC CCCCGCGCCAGGGAGAGAGTTCAGGAAAAGCGGGGGGAGAGGCCCACTGCCACTGCCACTCCCAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72959593..72959763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 112811 RMVar_ID_112811 Human_SNP_ID_825553009 m1A Human chr16 + 762723 762723 762723 CAACGGCTCGACCCCTGTTGGGGTCCTGTGGGACCCCCGCCCTCGGCAGCCTCCTGTTCCTGCTC CAACGGCTCGACCCCTGTTGGGGTCCTGTGGGGCCCCCGCCCTCGGCAGCCTCCTGTTCCTGCTC A G MSLN Ensembl:ENSG00000102854 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:762476..762725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_Splice_Rec_1656622,Human_Splice_Rec_1656623,Human_Splice_Rec_1656656,Human_Splice_Rec_1656657,Human_Splice_Rec_1656688,Human_Splice_Rec_1656689,Human_Splice_Rec_1656720,Human_Splice_Rec_1656721,Human_Splice_Rec_1656752,Human_Splice_Rec_1656753,Human_Splice_Rec_1656772,Human_Splice_Rec_1656773 112812 RMVar_ID_112812 Human_SNP_ID_825556258 m1A Human chr16 - 28982358 28982358 28982358 CTCCGGTCAGGCAGGTGATGAGTCCAAAGATGAGACTAGGGGTGAGGGAAGGGAATGGGGGGTTT CTCCGGTCAGGCAGGTGATGAGTCCAAAGATGGGACTAGGGGTGAGGGAAGGGAATGGGGGGTTT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:28982351..28982562 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung 112813 RMVar_ID_112813 Human_SNP_ID_825556295 m1A Human chr16 - 3069489 3069489 3069489 AGCAGGTTTTATTAAGATGCCAGGGCGACAGCACCAGGTCAGAGCTGCGGCAGGAACGCCAGGCA AGCAGGTTTTATTAAGATGCCAGGGCGACAGCGCCAGGTCAGAGCTGCGGCAGGAACGCCAGGCA T C MMP25-AS1,lnc-ZSCAN10-5,MMP25-AS1:2 RNACentral:URS0000D5DBB7,RNACentral:URS00008C07B2,RNACentral:URS00008B8F60 lincRNA,lincRNA,lincRNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:3069440..3069540 32194978 MeRIP-seq:(Medium) rs12449264 Functional Loss SNV ICGC 33..33 33 LICA 1 - 112814 RMVar_ID_112814 Human_SNP_ID_825559204 m1A Human chr16 + 2503868 2503868 2503868 AGGCGTGAGCCACCGCGCCTAGCCTATTTTTTAATTTTTTTGAATAGACCACTTTGTGCTGAATA AGGCGTGAGCCACCGCGCCTAGCCTATTTTTTTATTTTTTTGAATAGACCACTTTGTGCTGAATA A T AC093525.2,TBC1D24 Ensembl:ENSG00000260272,Ensembl:ENSG00000162065 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4786287 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_12703820 Clinvar_Rec_317 RMVar_hsa_circ_95560,RMVar_hsa_circ_110319,RMVar_hsa_circ_265739,RMVar_hsa_circ_175779,RMVar_hsa_circ_175780 112815 RMVar_ID_112815 Human_SNP_ID_825565897 m1A Human chr16 - 293697 293697 293697 TGTTCCCCAAGGTCTTCGGGGACGAGGAAGCCACAGCCCCATGAGAACTCCAGACCCTTGTCCCT TGTTCCCCAAGGTCTTCGGGGACGAGGAAGCCCCAGCCCCATGAGAACTCCAGACCCTTGTCCCT T G AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:293676..293725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_233369,Human_RBP_ID_3948284 Human_Splice_Rec_1653544,Human_Splice_Rec_1653560,Human_Splice_Rec_1653580 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_293011,RMVar_hsa_circ_175317,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783 112816 RMVar_ID_112816 Human_SNP_ID_825566313 m1A Human chr16 + 2460397 2460397 2460397 CGGCTGCTGCATGCCTGGTACGCGGACCCCGGACCCACTGGCCAGACCTCCCTCGGGCCCTCAGA CGGCTGCTGCATGCCTGGTACGCGGACCCCGGGCCCACTGGCCAGACCTCCCTCGGGCCCTCAGA A G TEDC2 Ensembl:ENSG00000162062 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2460376..2460451 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_27440471 112817 RMVar_ID_112817 Human_SNP_ID_825568646 m1A Human chr16 - 9091827 9091827 9091827 AACCAGGGACGACCCCCGCCCCAGGCCTTCCCACCCCCGGGCCCGGCCGAAGGTCGCCGCGGACC AACCAGGGACGACCCCCGCCCCAGGCCTTCCCCCCCCCGGGCCCGGCCGAAGGTCGCCGCGGACC T G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:9091743..9091948 26863410 MeRIP-seq:(Medium) rs1043005290 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 112818 RMVar_ID_112818 Human_SNP_ID_825580230 m1A Human chr16 - 30738710 30738710 30738710 AGGGTCTCAGGCCCAGGGACTGGGTCAGCCCCATTGGTTTTTCCCTTCAAGGTGGATGAGGGTGC AGGGTCTCAGGCCCAGGGACTGGGTCAGCCCCGTTGGTTTTTCCCTTCAAGGTGGATGAGGGTGC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30738663..30738764 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 112819 RMVar_ID_112819 Human_SNP_ID_825600768 m1A Human chr16 + 797991 797991 797991 TCAGGGACTTGCTCTAGTTCTCTGAGCCGCGGACATGCCCTCGCATTGCTTCCCGCAGAGTGCAG TCAGGGACTTGCTCTAGTTCTCTGAGCCGCGGCCATGCCCTCGCATTGCTTCCCGCAGAGTGCAG A C CHTF18 Ensembl:ENSG00000127586 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:793797..798050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_891089,Human_RBP_ID_1005753,Human_RBP_ID_1523640,Human_RBP_ID_8440476,Human_RBP_ID_12831681,Human_RBP_ID_18162847,Human_RBP_ID_18685669 112820 RMVar_ID_112820 Human_SNP_ID_825602758 m1A Human chr16 - 19702758 19702758 19702758 TTGATCTCTTGGCCTCATGATCCACCTACCTCAGCCTCCCAAAGTGTTGGTATTACAGGCATGAG TTGATCTCTTGGCCTCATGATCCACCTACCTCGGCCTCCCAAAGTGTTGGTATTACAGGCATGAG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 112821 RMVar_ID_112821 Human_SNP_ID_825608361 m1A Human chr16 + 30769507 30769507 30769507 GTGGATGCCCAGCTGCTGACTGTGCAGAAGCTAGAGGAGAAGGAGCGAGCCTTGCAGGGCAGCCT GTGGATGCCCAGCTGCTGACTGTGCAGAAGCTGGAGGAGAAGGAGCGAGCCTTGCAGGGCAGCCT A G RNF40 Ensembl:ENSG00000103549 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30769381..30769523 26863196 MeRIP-seq:(Medium) rs4889506 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_761145,Human_RBP_ID_891990,Human_RBP_ID_5114226,Human_RBP_ID_8812362,Human_RBP_ID_18419472,Human_RBP_ID_19071419,Human_RBP_ID_26328139,Human_RBP_ID_27811797 Human_Splice_Rec_1704174,Human_Splice_Rec_1704175,Human_Splice_Rec_1704226,Human_Splice_Rec_1704227,Human_Splice_Rec_1704260,Human_Splice_Rec_1704261,Human_Splice_Rec_1704303,Human_Splice_Rec_1704320,Human_Splice_Rec_1704321 Clinvar_Rec_443,Clinvar_Rec_444 RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970,RMVar_hsa_circ_177973,RMVar_hsa_circ_344728 112822 RMVar_ID_112822 Human_SNP_ID_825615567 m1A Human chr16 - 67195977 67195977 67195977 CACCACCTGTGGGGTCTGCCTTGATGGGCTCAAAGGAGGTAGAAGGGTTGGGTCCGGACGAACTG CACCACCTGTGGGGTCTGCCTTGATGGGCTCAGAGGAGGTAGAAGGGTTGGGTCCGGACGAACTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67195850..67196043 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 112823 RMVar_ID_112823 Human_SNP_ID_825615570 m1A Human chr16 - 67195977 67195977 67195977 CACCACCTGTGGGGTCTGCCTTGATGGGCTCAAAGGAGGTAGAAGGGTTGGGTCCGGACGAACTG CACCACCTGTGGGGTCTGCCTTGATGGGCTCACAGGAGGTAGAAGGGTTGGGTCCGGACGAACTG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67195850..67196043 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 112824 RMVar_ID_112824 Human_SNP_ID_825616075 m1A Human chr16 - 67443124 67443124 67443124 TTCAGAGCAGGACCTTGACGAGATGAACATCGAGATCATCCGCAACACCCTCTACAAGGTAATGC TTCAGAGCAGGACCTTGACGAGATGAACATCGGGATCATCCGCAACACCCTCTACAAGGTAATGC T C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_477566,Human_RBP_ID_888827,Human_RBP_ID_1520593,Human_RBP_ID_1844786,Human_RBP_ID_12775299 Human_Splice_Rec_1727412,Human_Splice_Rec_1727413,Human_Splice_Rec_1727426,Human_Splice_Rec_1727427,Human_Splice_Rec_1727438,Human_Splice_Rec_1727439,Human_Splice_Rec_1727454,Human_Splice_Rec_1727455,Human_Splice_Rec_1727470,Human_Splice_Rec_1727471,Human_Splice_Rec_1727490,Human_Splice_Rec_1727491,Human_Splice_Rec_1727504,Human_Splice_Rec_1727505,Human_Splice_Rec_1727514,Human_Splice_Rec_1727515,Human_Splice_Rec_1727521,Human_Splice_Rec_1727532,Human_Splice_Rec_1727533,Human_Splice_Rec_1727544,Human_Splice_Rec_1727545,Human_Splice_Rec_1727552,Human_Splice_Rec_1727553,Human_Splice_Rec_1727562 RMVar_hsa_circ_32849,RMVar_hsa_circ_179077,RMVar_hsa_circ_78030,RMVar_hsa_circ_276917,RMVar_hsa_circ_117044,RMVar_hsa_circ_119666,RMVar_hsa_circ_179078,RMVar_hsa_circ_179079,RMVar_hsa_circ_16833 112825 RMVar_ID_112825 Human_SNP_ID_825620300 m1A Human chr16 - 89696855 89696855 89696855 CACCGAGCTCCCCCCACCCCAAGCTCTGCTGGAGCCAATCTGCGGGGCTCTGCCGGGTGCACGGC CACCGAGCTCCCCCCACCCCAAGCTCTGCTGGGGCCAATCTGCGGGGCTCTGCCGGGTGCACGGC T C SPATA2L Ensembl:ENSG00000158792 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs462769 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma 35 head and neck Human_Splice_Rec_1753494 GWAS_ID_9534,GWAS_ID_9535,GWAS_ID_9536,GWAS_ID_9537,GWAS_ID_9538,GWAS_ID_9539,GWAS_ID_9540,GWAS_ID_9541 RMVar_hsa_circ_180673,RMVar_hsa_circ_107430 112826 RMVar_ID_112826 Human_SNP_ID_825629744 m1A Human chr16 + 57758682 57758682 57758682 CTGATGGCCCAGGCCTGCCAGGAAGAGCAGCCACCCCCGCCTTTCCGCCCATGCAATTTGCACTC CTGATGGCCCAGGCCTGCCAGGAAGAGCAGCCCCCCCCGCCTTTCCGCCCATGCAATTTGCACTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:57758633..57758857 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112827 RMVar_ID_112827 Human_SNP_ID_825632747 m1A Human chr16 + 30720296 30720296 30720296 CTGTTAGAAGTGGCTACTGCTCCTGACCCCCCACCCCGGCCCAAGCCAGTCAAGATGAAGGTCAA CTGTTAGAAGTGGCTACTGCTCCTGACCCCCCCCCCCGGCCCAAGCCAGTCAAGATGAAGGTCAA A C AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30720249..30720881 32194978 MeRIP-seq:(Medium) rs145842115 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 9 bladder,urinary tract,prostate Human_RBP_ID_233183,Human_RBP_ID_895757,Human_RBP_ID_5465890,Human_RBP_ID_5524352,Human_RBP_ID_8807078,Human_RBP_ID_12720101,Human_RBP_ID_18983659,Human_RBP_ID_20114827,Human_RBP_ID_24370664,Human_RBP_ID_26328909 Human_Splice_Rec_1703699,Human_Splice_Rec_1703757,Human_Splice_Rec_1703807,Human_Splice_Rec_1703851 RMVar_hsa_circ_99616,RMVar_hsa_circ_269023,RMVar_hsa_circ_177922,RMVar_hsa_circ_120311,RMVar_hsa_circ_117166,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_177923,RMVar_hsa_circ_120667,RMVar_hsa_circ_85283,RMVar_hsa_circ_177942,RMVar_hsa_circ_128037,RMVar_hsa_circ_177945,RMVar_hsa_circ_177946,RMVar_hsa_circ_79473,RMVar_hsa_circ_9612,RMVar_hsa_circ_20408,RMVar_hsa_circ_177947,RMVar_hsa_circ_112480,RMVar_hsa_circ_83042,RMVar_hsa_circ_115989,RMVar_hsa_circ_177949,RMVar_hsa_circ_177948,RMVar_hsa_circ_177953,RMVar_hsa_circ_80195,RMVar_hsa_circ_177954 112828 RMVar_ID_112828 Human_SNP_ID_825637991 m1A Human chr16 + 8855035 8855035 8855035 CCACACCTGCCCCCCATACCCCTTCCTCCAGGAGATACTTGAGAGGGACCATGCCCGGCTGAAGC CCACACCTGCCCCCCATACCCCTTCCTCCAGGGGATACTTGAGAGGGACCATGCCCGGCTGAAGC A G AC022167.2 Ensembl:ENSG00000260276 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:8854985..8855151 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_22653882,Human_RBP_ID_25241301 Human_Splice_Rec_1675810 RMVar_hsa_circ_366663 112829 RMVar_ID_112829 Human_SNP_ID_825639224 m1A Human chr16 + 27244656 27244655 27244656 ATCACCCGAGCATCGCCACATATGGCAGCTCCACAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG ATCACCCGAGCATCGCCACATATGGCAGCTCC_CAGAAAGGTTTGAACAGAGGCCCTGGCCAAAG CA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:27244652..27244731 26863196 MeRIP-seq:(Medium) rs35986918 Functional Loss DEL ICGC 33..33 33 ESCA 1 - GWAS_ID_7952,GWAS_ID_7953,GWAS_ID_7954,GWAS_ID_7955,GWAS_ID_7956,GWAS_ID_7957,GWAS_ID_7958,GWAS_ID_7959,GWAS_ID_7960,GWAS_ID_7961,GWAS_ID_7962,GWAS_ID_7963 112830 RMVar_ID_112830 Human_SNP_ID_825641802 m1A Human chr16 + 2933226 2933226 2933226 GTTCCTCTACAAGCGGGAGAAGGCTGTCGGGGACAAGGTGTATTGGACCTGCCGGGACCACGCGC GTTCCTCTACAAGCGGGAGAAGGCTGTCGGGGTCAAGGTGTATTGGACCTGCCGGGACCACGCGC A T FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2933176..2933400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_1667612,Human_Splice_Rec_1667636,Human_Splice_Rec_1667664 112831 RMVar_ID_112831 Human_SNP_ID_825648378 m1A Human chr16 - 69120497 69120497 69120497 CGCGAGACTGGCACCCGGTACCTGGTGACAGCACTCATCAAAGACAAGATCCTTTTCAAAACCCG CGCGAGACTGGCACCCGGTACCTGGTGACAGCGCTCATCAAAGACAAGATCCTTTTCAAAACCCG T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69120446..69120659 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_1005150,Human_RBP_ID_1520945,Human_RBP_ID_4379373,Human_RBP_ID_8437220,Human_RBP_ID_22442125,Human_RBP_ID_27244717 Human_miRNA_ID_1511433 112832 RMVar_ID_112832 Human_SNP_ID_825658075 m1A Human chr16 + 2930818 2930818 2930818 GGTGCTGAGCAAGCCGGCCCTGGAGGAGGAGGAGGCACCCCGAGCCCTGTCACTGCTGAGCCTGC GGTGCTGAGCAAGCCGGCCCTGGAGGAGGAGGCGGCACCCCGAGCCCTGTCACTGCTGAGCCTGC A C FLYWCH1 Ensembl:ENSG00000059122 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2930770..2930899 26863196 MeRIP-seq:(Medium) rs769636191 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_1667611,Human_Splice_Rec_1667635,Human_Splice_Rec_1667663 RMVar_hsa_circ_22370 112833 RMVar_ID_112833 Human_SNP_ID_825661787 m1A Human chr16 - 2253963 2253963 2253963 GGAGCCGCTCCAGCTCCAACTCCTCCCGATAAACAGGCCACTGAAGCTCTCGCCCCTGTAACTTA GGAGCCGCTCCAGCTCCAACTCCTCCCGATAACCAGGCCACTGAAGCTCTCGCCCCTGTAACTTA T G RNPS1 Ensembl:ENSG00000205937 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr16:2253901..2254075;chr16:2253876..2254025 31548705,26863196 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_470622,Human_RBP_ID_1003458,Human_RBP_ID_1281337,Human_RBP_ID_4397224,Human_RBP_ID_12690817,Human_RBP_ID_17253351,Human_RBP_ID_17369042,Human_RBP_ID_17485495,Human_RBP_ID_18284756,Human_RBP_ID_21888712,Human_RBP_ID_22440826,Human_RBP_ID_27440100 RMVar_hsa_circ_377688,RMVar_hsa_circ_175728 112834 RMVar_ID_112834 Human_SNP_ID_825667799 m1A Human chr16 + 1978650 1978650 1978650 ACATGAAGCTCCCTGTGCCGGCCGCCGCCCCCACCCCCTGGGAAACCCATAAAGGCGCACTGCCC ACATGAAGCTCCCTGTGCCGGCCGCCGCCCCCCCCCCCTGGGAAACCCATAAAGGCGCACTGCCC A C TBL3 Ensembl:ENSG00000183751 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1978602..1978680 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_1661250,Human_Splice_Rec_1661300,Human_Splice_Rec_1661342,Human_Splice_Rec_1661376,Human_Splice_Rec_1661408 RMVar_hsa_circ_113792,RMVar_hsa_circ_175605 112835 RMVar_ID_112835 Human_SNP_ID_825668465 m1A Human chr16 + 56519904 56519904 56519904 GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGACAAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC GGCTTAGGGGAGGAGGGCTGGAAGCTGGAGACCAGCGCAGCGGAGCTGGCCTCACGCGCCCGGGC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:56519854..56520009 26863196 MeRIP-seq:(Medium) rs78076550 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,meninges rhabdoid,LICA,large_intestine adenocarcinoma 11 large intestine,brain Clinvar_Rec_545,Clinvar_Rec_546 GWAS_ID_12576,GWAS_ID_12577,GWAS_ID_12578,GWAS_ID_12579,GWAS_ID_12580,GWAS_ID_12581,GWAS_ID_12582,GWAS_ID_12583,GWAS_ID_12584,GWAS_ID_12585 112836 RMVar_ID_112836 Human_SNP_ID_825673742 m1A Human chr16 - 16006889 16006889 16006889 CCACCATCATCATCACCATCGCCACCATCACCACCACCATCACCGCCACCGCCACCGCCACCGCC CCACCATCATCATCACCATCGCCACCATCACCGCCACCATCACCGCCACCGCCACCGCCACCGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:16006884..16006988 26863196 MeRIP-seq:(Medium) rs926455193 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,LMS,skin mycosis_fungoides-Sezary_syndrome 5 skin,haematopoietic and lymphoid tissue 112837 RMVar_ID_112837 Human_SNP_ID_825675489 m1A Human chr16 + 29805137 29805137 29805137 GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGAGGGCATAACGGGGAAACAGATGGAGTCCTTCC GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGCGGGCATAACGGGGAAACAGATGGAGTCCTTCC A C KIF22 Ensembl:ENSG00000079616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29804756..29805187 32194978 MeRIP-seq:(Medium) rs772351052 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 4 head and neck Human_RBP_ID_889614,Human_RBP_ID_5355750,Human_RBP_ID_9345801,Human_RBP_ID_18162097,Human_RBP_ID_18677166,Human_RBP_ID_18985966,Human_RBP_ID_19071287,Human_RBP_ID_22654074,Human_RBP_ID_22945023,Human_RBP_ID_23685997 Human_Splice_Rec_1699838,Human_Splice_Rec_1699839,Human_Splice_Rec_1699874,Human_Splice_Rec_1699875,Human_Splice_Rec_1699906,Human_Splice_Rec_1699907,Human_Splice_Rec_1699930,Human_Splice_Rec_1699931,Human_Splice_Rec_1699956,Human_Splice_Rec_1699957 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755 112838 RMVar_ID_112838 Human_SNP_ID_825677093 m1A Human chr16 - 88651006 88651006 88651006 GTGTCCCAGCCGGGTTCGTGTCGCCATGGGGCAGATCGAGTGGGCCATGTGGGCCAACGAACAGG GTGTCCCAGCCGGGTTCGTGTCGCCATGGGGCGGATCGAGTGGGCCATGTGGGCCAACGAACAGG T C CYBA Ensembl:ENSG00000051523 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88650883..88651075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_45973,Human_RBP_ID_233098,Human_RBP_ID_481498,Human_RBP_ID_1524656,Human_RBP_ID_4388944,Human_RBP_ID_5114359,Human_RBP_ID_5237389,Human_RBP_ID_5316929,Human_RBP_ID_9325441,Human_RBP_ID_17121851,Human_RBP_ID_18190191,Human_RBP_ID_18419489,Human_RBP_ID_18686656,Human_RBP_ID_22441167,Human_RBP_ID_26951679 Human_Splice_Rec_1749223,Human_Splice_Rec_1749237,Human_Splice_Rec_1749255,Human_Splice_Rec_1749265,Human_Splice_Rec_1749273,Human_Splice_Rec_1749279,Human_Splice_Rec_1749289,Human_Splice_Rec_1749295 RMVar_hsa_circ_79126,RMVar_hsa_circ_180504 112839 RMVar_ID_112839 Human_SNP_ID_825678941 m1A Human chr16 - 69316119 69316119 69316119 GCGGCAGCCTGAGGACCCCTCGTGTGACTCACACTTGATAGCGTGGAGGAAGTACTCCACCGCAT GCGGCAGCCTGAGGACCCCTCGTGTGACTCACGCTTGATAGCGTGGAGGAAGTACTCCACCGCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69316117..69316216 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 112840 RMVar_ID_112840 Human_SNP_ID_825678977 m1A Human chr16 - 70676888 70676888 70676888 CACCCAGCAGCTCCAGCTCCCGGAAGTCCAGCATGTGCAGGTCAGTGGGGGTGGGGTTCCCAGGG CACCCAGCAGCTCCAGCTCCCGGAAGTCCAGCGTGTGCAGGTCAGTGGGGGTGGGGTTCCCAGGG T C MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:70674439..70676892 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_233658,Human_RBP_ID_9064684,Human_RBP_ID_19075052 Human_Splice_Rec_1736042,Human_Splice_Rec_1736043,Human_Splice_Rec_1736064,Human_Splice_Rec_1736065,Human_Splice_Rec_1736076,Human_Splice_Rec_1736077,Human_Splice_Rec_1736088 RMVar_hsa_circ_115261,RMVar_hsa_circ_22883,RMVar_hsa_circ_179708,RMVar_hsa_circ_86405,RMVar_hsa_circ_372916,RMVar_hsa_circ_84703,RMVar_hsa_circ_89895,RMVar_hsa_circ_179713,RMVar_hsa_circ_179714,RMVar_hsa_circ_179715,RMVar_hsa_circ_93759,RMVar_hsa_circ_364581,RMVar_hsa_circ_179716,RMVar_hsa_circ_17940,RMVar_hsa_circ_50057,RMVar_hsa_circ_179717 112841 RMVar_ID_112841 Human_SNP_ID_825684738 m1A Human chr16 - 28836369 28836369 28836369 GACGGAGGGAAGCAAAGGACAGAGCCAGGAGCAAGCCCCTGGCGGCGGCGACTGTGGCTTCTGCC GACGGAGGGAAGCAAAGGACAGAGCCAGGAGCGAGCCCCTGGCGGCGGCGACTGTGGCTTCTGCC T C AC133550.2 Ensembl:ENSG00000260570 lincRNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:28836326..28836500 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 7 large intestine 112842 RMVar_ID_112842 Human_SNP_ID_825691631 m1A Human chr16 + 50261315 50261315 50261315 TCCTGGTAGAGGCGGCACCAGTACCTGGCGGGATGGGTAGCATTTTGAGCATTCCAGGGACACTA TCCTGGTAGAGGCGGCACCAGTACCTGGCGGGGTGGGTAGCATTTTGAGCATTCCAGGGACACTA A G ADCY7 Ensembl:ENSG00000121281 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:50261264..50261493 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112843 RMVar_ID_112843 Human_SNP_ID_825692698 m1A Human chr16 + 4114876 4114876 4114876 CCTGAGACAGGCGTCAAGACCTGGAACTGCGCAGCCAGGGTCAGGGCGAACACCAGCAGGGTGAG CCTGAGACAGGCGTCAAGACCTGGAACTGCGCGGCCAGGGTCAGGGCGAACACCAGCAGGGTGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr16:4114828..4114963;chr16:4114826..4114875 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 112844 RMVar_ID_112844 Human_SNP_ID_825699426 m1A Human chr16 + 23510445 23510413 23510445 GCTCCAGCCCCGACGCTGCGGCCGCGGGCGCCACTGCCTCTTCAGCCGCTGTAGCGTCCTGGCGC G________________________________CTGCCTCTTCAGCCGCTGTAGCGTCCTGGCGC GCTCCAGCCCCGACGCTGCGGCCGCGGGCGCCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr16:23510301..23510500;chr16:23510326..23510500 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 2..33 33 PRAD 1 - 112845 RMVar_ID_112845 Human_SNP_ID_825706924 m1A Human chr16 + 89518840 89518840 89518840 TGGTTGGATTGCCTCAGCTGCGGTGGGCACACACTGCGCGTGTGTCATGGGATGACCCCGGGGAG TGGTTGGATTGCCTCAGCTGCGGTGGGCACACCCTGCGCGTGTGTCATGGGATGACCCCGGGGAG A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89518790..89518900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5317073,Human_RBP_ID_22523485,Human_RBP_ID_22712761,Human_RBP_ID_26329448,Human_RBP_ID_27572773 RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,RMVar_hsa_circ_329655,RMVar_hsa_circ_180621,RMVar_hsa_circ_112642,RMVar_hsa_circ_180622,RMVar_hsa_circ_52897,RMVar_hsa_circ_107505,RMVar_hsa_circ_180623,RMVar_hsa_circ_180624 112846 RMVar_ID_112846 Human_SNP_ID_825712280 m1A Human chr16 + 77194494 77194494 77194494 TACACGTGCAAGTGTCGCCCGCATCTTCGCACACAAGCAGAACTATGACCTCCGCCGCCTGCTGG TACACGTGCAAGTGTCGCCCGCATCTTCGCACGCAAGCAGAACTATGACCTCCGCCGCCTGCTGG A G MON1B Ensembl:ENSG00000103111 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:77194356..77194606 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_1005614,Human_RBP_ID_23700857,Human_RBP_ID_27445791 112847 RMVar_ID_112847 Human_SNP_ID_825727599 m1A Human chr16 + 1826765 1826765 1826765 CGGCTCCCAGCGCGGCGAGGCTGCGGCGGCCGAGCAGCCCTCGGCCCACCACCATGACCCGGGCC CGGCTCCCAGCGCGGCGAGGCTGCGGCGGCCGGGCAGCCCTCGGCCCACCACCATGACCCGGGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1822328..1826825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 112848 RMVar_ID_112848 Human_SNP_ID_825730713 m1A Human chr16 + 30655083 30655083 30655083 CGGCACACTGTGGGTGGTGGGGAAATGGCCCGAGCCCCGCCACCCCCTCGGCCCTGTCTCCGGAA CGGCACACTGTGGGTGGTGGGGAAATGGCCCGTGCCCCGCCACCCCCTCGGCCCTGTCTCCGGAA A T PRR14 Ensembl:ENSG00000156858 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr16:30654951..30655200;chr16:30655036..30655155 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_472883,Human_RBP_ID_17371417,Human_RBP_ID_27240744 Human_miRNA_ID_2147063,Human_miRNA_ID_2988490,Human_miRNA_ID_3022189,Human_miRNA_ID_3066159 RMVar_hsa_circ_83847,RMVar_hsa_circ_117914,RMVar_hsa_circ_177903,RMVar_hsa_circ_177905,RMVar_hsa_circ_62512,RMVar_hsa_circ_177904,RMVar_hsa_circ_372460,RMVar_hsa_circ_121285,RMVar_hsa_circ_177906,RMVar_hsa_circ_93669,RMVar_hsa_circ_177909,RMVar_hsa_circ_82503,RMVar_hsa_circ_103261,RMVar_hsa_circ_177910,RMVar_hsa_circ_177912 112849 RMVar_ID_112849 Human_SNP_ID_825732614 m1A Human chr16 + 76277434 76277434 76277434 CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGTGAGAGAGAGAGAGAAAAGAGAGAGACAGAGACGG CTTTTCAGTGAGGAGTCAGGGAGGTGTGTGTGTGAGAGAGAGAGAAAAGAGAGAGACAGAGACGG A T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:76277383..76277480 26863196 MeRIP-seq:(Medium) rs1567554665 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 112850 RMVar_ID_112850 Human_SNP_ID_825741912 m1A Human chr16 + 24777068 24777068 24777068 AGCCAACAATCAGCAGCCACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC AGCCAACAATCAGCAGCCACAGCAGCAGCAGCCACAGCAGCAGCCGCAGCAGCAGCAGCCACAGC A C TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:24776880..24777162 26863196 MeRIP-seq:(Medium) rs4788428 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_895599,Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 112851 RMVar_ID_112851 Human_SNP_ID_825748539 m1A Human chr16 - 68352355 68352339 68352355 TGCAGCGAGGCTGCCTGGGGCATCACCATGGCACCTGGCCCCAGGTGCTGGTCCACAGCGGTCCG TGCAGCGAGGCTGCCTGGGGCATCACCATGGC________________TGGTCCACAGCGGTCCG AGCACCTGGGGCCAGGT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:68352304..68352431 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..48 33 LUSC 2 - 112852 RMVar_ID_112852 Human_SNP_ID_825751056 m1A Human chr16 - 58723888 58723888 58723888 ATGTGTTTCTCATTTCAGCTCCTGGTGGACCCATGTGGAAATGGGACCTCCAGATCCCATTCTGG ATGTGTTTCTCATTTCAGCTCCTGGTGGACCCGTGTGGAAATGGGACCTCCAGATCCCATTCTGG T C GOT2 Ensembl:ENSG00000125166 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:58723840..58723947 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 4 uterus Human_RBP_ID_894881,Human_RBP_ID_4401781 Human_Splice_Rec_1722274,Human_Splice_Rec_1722292,Human_Splice_Rec_1722310,Human_Splice_Rec_1722322,Human_Splice_Rec_1722336 RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_328817,RMVar_hsa_circ_178889,RMVar_hsa_circ_178892,RMVar_hsa_circ_374360,RMVar_hsa_circ_286995 112853 RMVar_ID_112853 Human_SNP_ID_825758049 m1A Human chr16 + 1809171 1809171 1809171 ATATGCATTAGAATGTCCGATAACACAAGCCAAGGGCTGTAAAATTAAGGTTAAATCAAGACTGA ATATGCATTAGAATGTCCGATAACACAAGCCACGGGCTGTAAAATTAAGGTTAAATCAAGACTGA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:1809126..1809400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 eye spindle 4 eye 112854 RMVar_ID_112854 Human_SNP_ID_825764116 m1A Human chr16 - 74360773 74360773 74360773 TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCATCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC TGGCAGAACTGGTCCTCTGCAAGAAACAGCGCGTCAGCTGCCGAGGCGCGTTCCATGGCCCTGCC T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs62055171 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_3510562,Human_RBP_ID_5096542,Human_RBP_ID_9373210,Human_RBP_ID_18529945,Human_RBP_ID_24371089 RMVar_hsa_circ_377905,RMVar_hsa_circ_107349,RMVar_hsa_circ_179924,RMVar_hsa_circ_295646,RMVar_hsa_circ_179928,RMVar_hsa_circ_179927,RMVar_hsa_circ_330711,RMVar_hsa_circ_19145,RMVar_hsa_circ_352828,RMVar_hsa_circ_358935,RMVar_hsa_circ_179933,RMVar_hsa_circ_179932,RMVar_hsa_circ_292513,RMVar_hsa_circ_303550 112855 RMVar_ID_112855 Human_SNP_ID_825783624 m1A Human chr16 + 16044679 16044679 16044679 ACCTGATGATGTTTTCCGGGCCGCAGATCTTAAAGTAAGACCCCTTCCCTCCCAGGTGGGCTCCA ACCTGATGATGTTTTCCGGGCCGCAGATCTTACAGTAAGACCCCTTCCCTCCCAGGTGGGCTCCA A C ABCC1 Ensembl:ENSG00000103222 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16044657..16044724 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_19073515 Human_Splice_Rec_1683109,Human_Splice_Rec_1683171,Human_Splice_Rec_1683227,Human_Splice_Rec_1683283 Human_miRNA_ID_2157873,Human_miRNA_ID_2157874,Human_miRNA_ID_2157875,Human_miRNA_ID_2385177,Human_miRNA_ID_2385178,Human_miRNA_ID_2385179 RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488,RMVar_hsa_circ_315,RMVar_hsa_circ_29597,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_373728,RMVar_hsa_circ_370458,RMVar_hsa_circ_362371,RMVar_hsa_circ_340715,RMVar_hsa_circ_88994,RMVar_hsa_circ_64508,RMVar_hsa_circ_114958,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_116070,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609,RMVar_hsa_circ_45957,RMVar_hsa_circ_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_269678,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_37879,RMVar_hsa_circ_176619,RMVar_hsa_circ_347337,RMVar_hsa_circ_370295,RMVar_hsa_circ_303867,RMVar_hsa_circ_17801,RMVar_hsa_circ_279065,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176621,RMVar_hsa_circ_106663,RMVar_hsa_circ_370894,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176627,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_176626,RMVar_hsa_circ_23834,RMVar_hsa_circ_306705,RMVar_hsa_circ_326399,RMVar_hsa_circ_344358,RMVar_hsa_circ_372789,RMVar_hsa_circ_373331,RMVar_hsa_circ_359208,RMVar_hsa_circ_337336,RMVar_hsa_circ_317666,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176632,RMVar_hsa_circ_176634,RMVar_hsa_circ_176635,RMVar_hsa_circ_176633,RMVar_hsa_circ_176631 112856 RMVar_ID_112856 Human_SNP_ID_825793914 m1A Human chr16 - 16007921 16007921 16007921 TCGGTCATGTCGGGAGAGATAGAGGAAGTAGAAGGGGAAACAGGCCCAGAGGTAAAAACAAGGCA TCGGTCATGTCGGGAGAGATAGAGGAAGTAGAGGGGGAAACAGGCCCAGAGGTAAAAACAAGGCA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:16007719..16007925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 112857 RMVar_ID_112857 Human_SNP_ID_825824189 m1A Human chr16 + 1999639 1999639 1999639 TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCATGTGTCCATTAACGACGACGGCAACTGGCCCC TGGGGGCACTCCGAGCAGGGGCCGGGCCCTCCGTGTGTCCATTAACGACGACGGCAACTGGCCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:1999501..1999730 26863196 MeRIP-seq:(Medium) rs2286469 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 13 caecum,head and neck,large intestine GWAS_ID_8864,GWAS_ID_8865,GWAS_ID_8866,GWAS_ID_8867,GWAS_ID_8868,GWAS_ID_8869,GWAS_ID_8870,GWAS_ID_8871,GWAS_ID_8872,GWAS_ID_8873 112858 RMVar_ID_112858 Human_SNP_ID_825826301 m1A Human chr16 - 30429961 30429961 30429961 AGCGGTGGGCGGCATGTCTGTGGCCGGTGGGGAGATTCGTGGGGACACGGGGGGAGAGGACACTG AGCGGTGGGCGGCATGTCTGTGGCCGGTGGGGGGATTCGTGGGGACACGGGGGGAGAGGACACTG T C DCTPP1 Ensembl:ENSG00000179958 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:30429830..30430025;chr16:30429810..30430050;chr16:30429830..30430050;chr16:30429821..30430025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 5 haematopoietic and lymphoid tissue Human_RBP_ID_234210,Human_RBP_ID_762082,Human_RBP_ID_818336,Human_RBP_ID_4393013,Human_RBP_ID_5141891,Human_RBP_ID_5316641,Human_RBP_ID_5464974,Human_RBP_ID_6507811,Human_RBP_ID_8806930,Human_RBP_ID_9061764,Human_RBP_ID_9325068,Human_RBP_ID_17875389,Human_RBP_ID_18437517,Human_RBP_ID_21888834,Human_RBP_ID_22440974,Human_RBP_ID_23209327,Human_RBP_ID_23686584,Human_RBP_ID_27240556 Human_Splice_Rec_1703031,Human_Splice_Rec_1703035 RMVar_hsa_circ_122935,RMVar_hsa_circ_177880 112859 RMVar_ID_112859 Human_SNP_ID_825826641 m1A Human chr16 - 89291180 89291180 89291180 CCTCCCTCTCTCCCTCGCCCGCCTCACAGAGAAGCAGGGCCCTGAGCGGAAGAGGATTAAGAAGG CCTCCCTCTCTCCCTCGCCCGCCTCACAGAGACGCAGGGCCCTGAGCGGAAGAGGATTAAGAAGG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:89291074..89291220;chr16:89291085..89291214 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 10 ovary Human_RBP_ID_5358754,Human_RBP_ID_6546106,Human_RBP_ID_22541966,Human_RBP_ID_22652589,Human_RBP_ID_25241200,Human_RBP_ID_27811344 Human_Splice_Rec_1750726,Human_Splice_Rec_1750750,Human_Splice_Rec_1750770,Human_Splice_Rec_1750792,Human_Splice_Rec_1750816,Human_Splice_Rec_1750858,Human_Splice_Rec_1750876,Human_Splice_Rec_1750900,Human_Splice_Rec_1750916,Human_Splice_Rec_1750928,Human_Splice_Rec_1750940,Human_Splice_Rec_1750954,Human_Splice_Rec_1750964,Human_Splice_Rec_1750978,Human_Splice_Rec_1750990,Human_Splice_Rec_1751006,Human_Splice_Rec_1751014,Human_Splice_Rec_1751022 Human_miRNA_ID_2354149,Human_miRNA_ID_2381266,Human_miRNA_ID_2574437,Human_miRNA_ID_3024275 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_180610,RMVar_hsa_circ_34833,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574,RMVar_hsa_circ_180609,RMVar_hsa_circ_335554 112860 RMVar_ID_112860 Human_SNP_ID_825832815 m1A Human chr16 - 2135083 2135083 2135083 GGCGGCAGGGAAGAGTTCCAGGAGGTGTCTGGAAAAGGATTTGATGGATGTGCAAGAATTGGGCT GGCGGCAGGGAAGAGTTCCAGGAGGTGTCTGGGAAAGGATTTGATGGATGTGCAAGAATTGGGCT T C PKD1 Ensembl:ENSG00000008710 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2135032..2135352 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_3504140,Human_RBP_ID_8184215,Human_RBP_ID_18938653 RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 112861 RMVar_ID_112861 Human_SNP_ID_825835222 m1A Human chr16 + 67438475 67438475 67438475 GACCACATACACACACACGCACACACACGCGCACACACACACACACACACACAAAGAGTGCAATT GACCACATACACACACACGCACACACACGCGCGCACACACACACACACACACAAAGAGTGCAATT A G NONHSAG019743.2 RNACentral:URS00009BC955 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67438425..67438502 26863196 MeRIP-seq:(Medium) rs72650133 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 112862 RMVar_ID_112862 Human_SNP_ID_825843337 m1A Human chr16 + 50154040 50154040 50154040 GTCCTCGCCTCCCTCGGCGTCCTCGTCCCCGCACCCTTCGGCCGCCGTCCCCGCCGCCGATCCAG GTCCTCGCCTCCCTCGGCGTCCTCGTCCCCGCCCCCTTCGGCCGCCGTCCCCGCCGCCGATCCAG A C TENT4B Ensembl:ENSG00000121274 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:50153989..50154199 26863196 MeRIP-seq:(Medium) rs879227372 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_893602 RMVar_hsa_circ_79929,RMVar_hsa_circ_178299 112863 RMVar_ID_112863 Human_SNP_ID_825856072 m1A Human chr16 - 72787739 72787739 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCGGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC T C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs200561133 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 112864 RMVar_ID_112864 Human_SNP_ID_825861405 m1A Human chr16 + 28487699 28487699 28487699 GGGCAGCAGGTGAAGGCCAAGAGGAGCCAACAATTTGATGACGAGTGTGGGGAGGATGTCCGCCA GGGCAGCAGGTGAAGGCCAAGAGGAGCCAACATTTTGATGACGAGTGTGGGGAGGATGTCCGCCA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:28486643..28487718 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 15 large intestine 112865 RMVar_ID_112865 Human_SNP_ID_825863498 m1A Human chr16 + 520197 520188 520197 TCAAGCTGGAGGCCGAGCAGCGGCGGGGCCGCAGCAGCAGCATGGGCCTGCAGGAGTACCACAGC TCAAGCTGGAGGCCGAGCAGCGGC_________GCAGCAGCATGGGCCTGCAGGAGTACCACAGC CGGGGCCGCA C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:520135..520218 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 25..33 33 LIHC 1 - Human_Splice_Rec_1654050,Human_Splice_Rec_1654051,Human_Splice_Rec_1654076,Human_Splice_Rec_1654077,Human_Splice_Rec_1654098,Human_Splice_Rec_1654099 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_79967,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_265064,RMVar_hsa_circ_175370 112866 RMVar_ID_112866 Human_SNP_ID_825870102 m1A Human chr16 - 22195726 22195726 22195726 TAGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACACCTCAGAAGGTCTCA TAGGCTCCAGTCATTTCGATGGCGTGGGTTCGCATCCCACCGCTGCCACACCTCAGAAGGTCTCA T G tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1288217953 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_269744,Human_RBP_ID_277311,Human_RBP_ID_470365,Human_RBP_ID_1003412,Human_RBP_ID_1177312,Human_RBP_ID_1281298,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_2470564,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5274765,Human_RBP_ID_5419054,Human_RBP_ID_5440235,Human_RBP_ID_5464787,Human_RBP_ID_5495261,Human_RBP_ID_6499986,Human_RBP_ID_8251997,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9286591,Human_RBP_ID_9842114,Human_RBP_ID_12688447,Human_RBP_ID_17253321,Human_RBP_ID_17369012,Human_RBP_ID_17485449,Human_RBP_ID_17689826,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178808,Human_RBP_ID_18199987,Human_RBP_ID_18437270,Human_RBP_ID_18512948,Human_RBP_ID_18529668,Human_RBP_ID_18674881,Human_RBP_ID_20102940,Human_RBP_ID_22048930,Human_RBP_ID_22198161,Human_RBP_ID_22800228,Human_RBP_ID_22945424,Human_RBP_ID_23127966,Human_RBP_ID_23163312,Human_RBP_ID_23682595,Human_RBP_ID_24412972,Human_RBP_ID_24477477,Human_RBP_ID_25241957,Human_RBP_ID_26446513,Human_RBP_ID_26748952,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439974,Human_RBP_ID_27657284 112867 RMVar_ID_112867 Human_SNP_ID_825885569 m1A Human chr16 + 28836160 28836160 28836160 CAGCCTGGCCAGGCGCCTGGATTTCCAGGAGGAGCCGATGACAGGATTCGTGAGTTCTCATTAGC CAGCCTGGCCAGGCGCCTGGATTTCCAGGAGGGGCCGATGACAGGATTCGTGAGTTCTCATTAGC A G ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28836151..28836225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_888581,Human_RBP_ID_1515970,Human_RBP_ID_5355727,Human_RBP_ID_8431474,Human_RBP_ID_12712345,Human_RBP_ID_17874773,Human_RBP_ID_19071236,Human_RBP_ID_22356361,Human_RBP_ID_22654045,Human_RBP_ID_22800739,Human_RBP_ID_22937958 Human_Splice_Rec_1697721,Human_Splice_Rec_1697765,Human_Splice_Rec_1697897,Human_Splice_Rec_1697941 112868 RMVar_ID_112868 Human_SNP_ID_825899080 m1A Human chr16 + 1777180 1777180 1777180 GGGGTGGGCGGAGGTCGCTGCCTGGGGATCGGACACTGGAGCCTTGCGGCGGCTGCAACTCATGC GGGGTGGGCGGAGGTCGCTGCCTGGGGATCGGGCACTGGAGCCTTGCGGCGGCTGCAACTCATGC A G EME2 Ensembl:ENSG00000197774 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1777001..1777443 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_5357305,Human_RBP_ID_8084583,Human_RBP_ID_22714185 112869 RMVar_ID_112869 Human_SNP_ID_825900295 m1A Human chr16 - 47504814 47504814 47504814 GACTGGAGAGGCCTCGGGATCCCACCTCAGCCAGGGAGTGCGCTGGCCTTCACCTTCACTGCGCC GACTGGAGAGGCCTCGGGATCCCACCTCAGCCGGGGAGTGCGCTGGCCTTCACCTTCACTGCGCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:47504706..47504875 26863196 MeRIP-seq:(Medium) rs796670787 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 6 brain 112870 RMVar_ID_112870 Human_SNP_ID_825903819 m1A Human chr16 - 11796342 11796342 11796342 GGACCTTGCCATGCCCAGTACGGTGGCCACTGACCCCCCGCCGTTTGGGACGATGGAGCCCACGA GGACCTTGCCATGCCCAGTACGGTGGCCACTGCCCCCCCGCCGTTTGGGACGATGGAGCCCACGA T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11796329..11796624 26863196 MeRIP-seq:(Medium) rs1048166252 Functional Loss SNV ICGC 33..33 33 SKCA 3 - Human_Splice_Rec_1678492,Human_Splice_Rec_1678500 112871 RMVar_ID_112871 Human_SNP_ID_825904702 m1A Human chr16 - 75265928 75265928 75265928 CTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGACCCCTCGCGGGGCCTCTGAGCGGCGCGGGCGG CTCAGGAGCCGGAGGAGCCGGAAAGCGCCGGGCCCCCTCGCGGGGCCTCTGAGCGGCGCGGGCGG T G BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:75265213..75266000;chr16:75265213..75265975;chr16:75265779..75265975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_4393257,Human_RBP_ID_22944891 112872 RMVar_ID_112872 Human_SNP_ID_825908898 m1A Human chr16 - 1817235 1817235 1817235 CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTATGAAGGGACTGCGGATGAGATGTGTAAAGCTC CACCTTGTTTGTGGCTGGCTGCGGGAAGTTCTGTGAAGGGACTGCGGATGAGATGTGTAAAGCTC T C HAGH Ensembl:ENSG00000063854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1817226..1817250 26863196 MeRIP-seq:(Medium) rs144037672 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_815813,Human_RBP_ID_4353078,Human_RBP_ID_19070502,Human_RBP_ID_27811464 Human_Splice_Rec_1660762,Human_Splice_Rec_1660763,Human_Splice_Rec_1660786,Human_Splice_Rec_1660787,Human_Splice_Rec_1660800,Human_Splice_Rec_1660801,Human_Splice_Rec_1660818,Human_Splice_Rec_1660819,Human_Splice_Rec_1660838,Human_Splice_Rec_1660839,Human_Splice_Rec_1660854 Human_miRNA_ID_2195870,Human_miRNA_ID_2210678,Human_miRNA_ID_2534845,Human_miRNA_ID_2536577 RMVar_hsa_circ_85120,RMVar_hsa_circ_128139,RMVar_hsa_circ_175564,RMVar_hsa_circ_175561,RMVar_hsa_circ_84877,RMVar_hsa_circ_175562,RMVar_hsa_circ_175560,RMVar_hsa_circ_329682,RMVar_hsa_circ_326110,RMVar_hsa_circ_327993,RMVar_hsa_circ_175565 112873 RMVar_ID_112873 Human_SNP_ID_825910329 m1A Human chr16 + 190003 190003 190003 TATTTCGCACTTCGGTCCCGGGAAGCCCGACGATGTCCCCGGCTGTGGCTCCGGGAACGGCTGCG TATTTCGCACTTCGGTCCCGGGAAGCCCGACGGTGTCCCCGGCTGTGGCTCCGGGAACGGCTGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:189972..190076 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 112874 RMVar_ID_112874 Human_SNP_ID_825911287 m1A Human chr16 + 4852827 4852827 4852827 TCTTAAACTTAAATCTCTTTAATTAGGCAGGTAAACTATTTTATCATCTTCGTTTGACCTGGCCC TCTTAAACTTAAATCTCTTTAATTAGGCAGGTGAACTATTTTATCATCTTCGTTTGACCTGGCCC A G UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4852822..4853037 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 5 lung Human_RBP_ID_8434587 RMVar_hsa_circ_76543,RMVar_hsa_circ_176075 112875 RMVar_ID_112875 Human_SNP_ID_825912694 m1A Human chr16 - 29813966 29813966 29813966 TATTGCAGCGCTGGCGGGAAGCTGGGAGCCACAGCAGGCCTGGGCTAGGGTCCCATGGGGCTCAC TATTGCAGCGCTGGCGGGAAGCTGGGAGCCACCGCAGGCCTGGGCTAGGGTCCCATGGGGCTCAC T G AC009133.1 Ensembl:ENSG00000238045 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29813915..29814460 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 11 haematopoietic and lymphoid tissue Human_RBP_ID_5182677 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 112876 RMVar_ID_112876 Human_SNP_ID_825918916 m1A Human chr16 + 4813749 4813749 4813749 AGCCCAAGGAAGGCTGCTACCTGGGCCAGCTCAGTGACGGTGTCAGCGTCCACTGTTGACATGTC AGCCCAAGGAAGGCTGCTACCTGGGCCAGCTCGGTGACGGTGTCAGCGTCCACTGTTGACATGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4812098..4813835 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 112877 RMVar_ID_112877 Human_SNP_ID_825920675 m1A Human chr16 - 3731901 3731899 3731902 GTCAGGGCGACAGCAAGAATGCCAAGAAGAAGAACAACAAGAAAACCAACAAGAACAAAAGCAGC GTCAGGGCGACAGCAAGAATGCCAAGAAGAA___CAACAAGAAAACCAACAAGAACAAAAGCAGC GTTC G CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:3731851..3731925 26863196 MeRIP-seq:(Medium) rs751071525 Functional Loss DEL TCGA,ICGC 32..34 33 STAD,UCEC 2 - Human_RBP_ID_9372155,Human_RBP_ID_24544677,Human_RBP_ID_26328576 Human_Splice_Rec_1670782,Human_Splice_Rec_1670840,Human_Splice_Rec_1670850,Human_Splice_Rec_1670858 RMVar_hsa_circ_34329,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959 112878 RMVar_ID_112878 Human_SNP_ID_825922151 m1A Human chr16 + 88825079 88825079 88825079 TGGGCGGCCGGGGCTGGAGCTCCTGGGTGGCCAGGGCTGGGGTGACTGGGTATCTGGGGCGCCTG TGGGCGGCCGGGGCTGGAGCTCCTGGGTGGCCGGGGCTGGGGTGACTGGGTATCTGGGGCGCCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:88825060..88825395 26863196 MeRIP-seq:(Medium) rs1327781720 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver 112879 RMVar_ID_112879 Human_SNP_ID_825929158 m1A Human chr16 - 31473473 31473473 31473473 CTCTTTGGGAGCCCCTGACCTTGGCATGTGCGAGGTGGTAGTCTCCAGGTCAGAGAGCAGGGCAT CTCTTTGGGAGCCCCTGACCTTGGCATGTGCGCGGTGGTAGTCTCCAGGTCAGAGAGCAGGGCAT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31473457..31473533 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 112880 RMVar_ID_112880 Human_SNP_ID_825932150 m1A Human chr16 + 89907856 89907856 89907856 CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAATTCCCACCTCCCAGCTCCCAGTTCCCACCTCC CTCCCACCTCACCTCCCTCCTCCCTCCTTCCAGTTCCCACCTCCCAGCTCCCAGTTCCCACCTCC A G TCF25,AC092143.3 Ensembl:ENSG00000141002,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:89907854..89908805 26863196 MeRIP-seq:(Medium) rs200953853 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_3505953,Human_RBP_ID_5128333,Human_RBP_ID_17077778,Human_RBP_ID_18939789 RMVar_hsa_circ_116682,RMVar_hsa_circ_180779,RMVar_hsa_circ_180787,RMVar_hsa_circ_86300,RMVar_hsa_circ_180789,RMVar_hsa_circ_121737,RMVar_hsa_circ_120186,RMVar_hsa_circ_110686,RMVar_hsa_circ_93594,RMVar_hsa_circ_180793,RMVar_hsa_circ_180794,RMVar_hsa_circ_86326,RMVar_hsa_circ_117869,RMVar_hsa_circ_180801,RMVar_hsa_circ_292382,RMVar_hsa_circ_180802,RMVar_hsa_circ_180804,RMVar_hsa_circ_180803,RMVar_hsa_circ_117937,RMVar_hsa_circ_82158,RMVar_hsa_circ_105834,RMVar_hsa_circ_180816,RMVar_hsa_circ_180815,RMVar_hsa_circ_180826,RMVar_hsa_circ_88147,RMVar_hsa_circ_180828,RMVar_hsa_circ_89714,RMVar_hsa_circ_105751,RMVar_hsa_circ_180832,RMVar_hsa_circ_180833,RMVar_hsa_circ_88876,RMVar_hsa_circ_10893,RMVar_hsa_circ_106580,RMVar_hsa_circ_180834,RMVar_hsa_circ_180836,RMVar_hsa_circ_108349,RMVar_hsa_circ_180837 112881 RMVar_ID_112881 Human_SNP_ID_825935796 m1A Human chr16 + 25259120 25259120 25259120 GAAGACCTGGGATTGATAGAAAGGAAGTGTTCAGGTTAAGATAAAAGATAGTGGAGACTAAGGTT GAAGACCTGGGATTGATAGAAAGGAAGTGTTCGGGTTAAGATAAAAGATAGTGGAGACTAAGGTT A G ZKSCAN2-DT Ensembl:ENSG00000274925 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:25259042..25259125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112882 RMVar_ID_112882 Human_SNP_ID_825955042 m1A Human chr16 - 31061732 31061732 31061732 GGAGCGCCCCTTCCACTGTAACGCATGTGGGAAATCCTTTGTGGTGTCGTCGAGCCTGAGGAAGC GGAGCGCCCCTTCCACTGTAACGCATGTGGGACATCCTTTGTGGTGTCGTCGAGCCTGAGGAAGC T G ZNF668 Ensembl:ENSG00000167394 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31061639..31061889 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus RMVar_hsa_circ_111739,RMVar_hsa_circ_178001,RMVar_hsa_circ_99732,RMVar_hsa_circ_178002 112883 RMVar_ID_112883 Human_SNP_ID_825959720 m1A Human chr16 + 1685563 1685563 1685563 ATATTTTTGGACCAACAGAAGAACCTCAGAACATACCCAAGAGGACAAATCCCCCAGGTATGGGC ATATTTTTGGACCAACAGAAGAACCTCAGAACGTACCCAAGAGGACAAATCCCCCAGGTATGGGC A G AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding 3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1685512..1691867 32194978 MeRIP-seq:(Medium) rs909750885 Functional Loss SNV ICGC 33..33 33 SARC 1 - Human_RBP_ID_891136,Human_RBP_ID_1003046,Human_RBP_ID_1512966,Human_RBP_ID_1838585,Human_RBP_ID_3491885,Human_RBP_ID_5113794,Human_RBP_ID_6496138,Human_RBP_ID_9372041,Human_RBP_ID_12677011,Human_RBP_ID_17652540,Human_RBP_ID_17872292,Human_RBP_ID_18529642,Human_RBP_ID_19070458,Human_RBP_ID_22048556,Human_RBP_ID_26328026,Human_RBP_ID_26445605,Human_RBP_ID_27439373 Human_Splice_Rec_1659983,Human_Splice_Rec_1659993,Human_Splice_Rec_1659999,Human_Splice_Rec_1660007,Human_Splice_Rec_1660013,Human_Splice_Rec_1660023,Human_Splice_Rec_1660031,Human_Splice_Rec_1660043,Human_Splice_Rec_1660053,Human_Splice_Rec_1660059,Human_Splice_Rec_1660067,Human_Splice_Rec_1660073,Human_Splice_Rec_1660079,Human_Splice_Rec_1660083 Human_miRNA_ID_1191895,Human_miRNA_ID_1191896,Human_miRNA_ID_2255325,Human_miRNA_ID_2571117,Human_miRNA_ID_3044853 RMVar_hsa_circ_175534,RMVar_hsa_circ_295159,RMVar_hsa_circ_291871,RMVar_hsa_circ_36676,RMVar_hsa_circ_356801,RMVar_hsa_circ_357002,RMVar_hsa_circ_283954 112884 RMVar_ID_112884 Human_SNP_ID_825973127 m1A Human chr16 + 2763004 2763004 2763004 GTCGCTCCAGTTCTTCTCCGCCACCTAAACAGAAATCTAAGACACCATCAAGACAAAGTCATTCC GTCGCTCCAGTTCTTCTCCGCCACCTAAACAGTAATCTAAGACACCATCAAGACAAAGTCATTCC A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2762900..2763079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_1515524,Human_RBP_ID_1840705,Human_RBP_ID_6505322,Human_RBP_ID_8806346,Human_RBP_ID_17253663,Human_RBP_ID_17369323,Human_RBP_ID_18529709,Human_RBP_ID_18676457,Human_RBP_ID_20093634,Human_RBP_ID_22800525,Human_RBP_ID_27239668 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 112885 RMVar_ID_112885 Human_SNP_ID_825984564 m1A Human chr16 + 30080991 30080991 30080991 GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGAGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA GTCCTGGATGCGGAAGAGGGAGCGGCAGGGGGGGTCAGGGCTGGAAAAGTCCCAGCCTGCTCAGA A G PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30080982..30081300 26863196 MeRIP-seq:(Medium) rs200223896 Functional Loss SNV ICGC 33..33 33 SKCA 2 - RMVar_hsa_circ_77528,RMVar_hsa_circ_102602,RMVar_hsa_circ_117378,RMVar_hsa_circ_177833,RMVar_hsa_circ_109929,RMVar_hsa_circ_177834,RMVar_hsa_circ_177836,RMVar_hsa_circ_177835 112886 RMVar_ID_112886 Human_SNP_ID_825984737 m1A Human chr16 + 29830528 29830528 29830528 CGTCTCCCCCACCTACCAGTCATCTTCTTGTGAGCCCTGGGCTTAGGAGTCACCATGGCAACTGA CGTCTCCCCCACCTACCAGTCATCTTCTTGTGGGCCCTGGGCTTAGGAGTCACCATGGCAACTGA A G AC120114.4,MVP Ensembl:ENSG00000281348,Ensembl:ENSG00000013364 Protein coding,Protein coding 3'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29830518..29830702 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_760416 Human_Splice_Rec_1700158,Human_Splice_Rec_1700160,Human_Splice_Rec_1700170,Human_Splice_Rec_1700198,Human_Splice_Rec_1700206,Human_Splice_Rec_1700234,Human_Splice_Rec_1700238,Human_Splice_Rec_1700242,Human_Splice_Rec_1700248,Human_Splice_Rec_1700256,Human_Splice_Rec_1700262,Human_Splice_Rec_1700268,Human_Splice_Rec_1700272,Human_Splice_Rec_1700278,Human_Splice_Rec_1700282 Human_miRNA_ID_2780045 RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_80277,RMVar_hsa_circ_59024,RMVar_hsa_circ_177766,RMVar_hsa_circ_177764,RMVar_hsa_circ_375764,RMVar_hsa_circ_342513 112887 RMVar_ID_112887 Human_SNP_ID_825985327 m1A Human chr16 - 89962127 89962127 89962127 CCCCCGCCCCCCACTTCCATGGCCCCAGCCTCACGCGAATCTCCACCAGCTCCTCCACGTAGCTG CCCCCGCCCCCCACTTCCATGGCCCCAGCCTCCCGCGAATCTCCACCAGCTCCTCCACGTAGCTG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89962100..89963841 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 face Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 7 skin,head and neck 112888 RMVar_ID_112888 Human_SNP_ID_825985380 m1A Human chr16 + 29985773 29985773 29985773 GGCGGAGGAGGAAGCAGGGCTGCTGCGGCGGCAGCGCCAGTACTTTGAGCTGCAGTGTCGCCAGT GGCGGAGGAGGAAGCAGGGCTGCTGCGGCGGCTGCGCCAGTACTTTGAGCTGCAGTGTCGCCAGT A T TAOK2 Ensembl:ENSG00000149930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29985725..29985796 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_233836,Human_RBP_ID_26329981,Human_RBP_ID_27811029 Human_Splice_Rec_1700795,Human_Splice_Rec_1700825,Human_Splice_Rec_1700857,Human_Splice_Rec_1700877,Human_Splice_Rec_1700881 RMVar_hsa_circ_10750,RMVar_hsa_circ_81886,RMVar_hsa_circ_377391,RMVar_hsa_circ_2067,RMVar_hsa_circ_107373,RMVar_hsa_circ_177806,RMVar_hsa_circ_177807,RMVar_hsa_circ_6579 112889 RMVar_ID_112889 Human_SNP_ID_825992728 m1A Human chr16 - 29694679 29694679 29694679 TGTCCACCAGGGCTGCCAGGGTGACGGGCGGCAGCAGCAGCGCCAGGCCTGGGGGGAAGAGAGAA TGTCCACCAGGGCTGCCAGGGTGACGGGCGGCGGCAGCAGCGCCAGGCCTGGGGGGAAGAGAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:29679151..29695856;chr16:29679057..29695806 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 112890 RMVar_ID_112890 Human_SNP_ID_825997198 m1A Human chr16 + 138354 138354 138354 AGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGAGGCGGAGGGGGCCTGAGGAGGACGAGGCGGGG AGGCGGAGGGGGCCTGAGGAGGACGGAGCCGGGGGCGGAGGGGGCCTGAGGAGGACGAGGCGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:138151..138415 26863196 MeRIP-seq:(Medium) rs1229931842 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 3 oesophagus 112891 RMVar_ID_112891 Human_SNP_ID_826000235 m1A Human chr16 + 2081770 2081770 2081770 TCACTGTCGGTGCCGGCAGCCAGCACGGCCAAACCCCCTCCTCTGCCTCGCTCCAACACAGGTGA TCACTGTCGGTGCCGGCAGCCAGCACGGCCAACCCCCCTCCTCTGCCTCGCTCCAACACAGGTGA A C TSC2 Ensembl:ENSG00000103197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2081721..2081817 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 15 caecum,large intestine Human_Splice_Rec_1661923,Human_Splice_Rec_1662003,Human_Splice_Rec_1662105,Human_Splice_Rec_1662281,Human_Splice_Rec_1662361,Human_Splice_Rec_1662441,Human_Splice_Rec_1662519,Human_Splice_Rec_1662627,Human_Splice_Rec_1662751,Human_Splice_Rec_1662831,Human_Splice_Rec_1662915,Human_Splice_Rec_1662985,Human_Splice_Rec_1663093,Human_Splice_Rec_1663173,Human_Splice_Rec_1663251,Human_Splice_Rec_1663331,Human_Splice_Rec_1663409,Human_Splice_Rec_1663555,Human_Splice_Rec_1663645,Human_Splice_Rec_1663719,Human_Splice_Rec_1663779,Human_Splice_Rec_1663807,Human_Splice_Rec_1663837,Human_Splice_Rec_1663883,Human_Splice_Rec_1663905 RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_82864,RMVar_hsa_circ_81580,RMVar_hsa_circ_175626,RMVar_hsa_circ_175630,RMVar_hsa_circ_110039,RMVar_hsa_circ_175634,RMVar_hsa_circ_105492,RMVar_hsa_circ_121572,RMVar_hsa_circ_175640,RMVar_hsa_circ_103353,RMVar_hsa_circ_175641,RMVar_hsa_circ_175639,RMVar_hsa_circ_2424,RMVar_hsa_circ_35823 112892 RMVar_ID_112892 Human_SNP_ID_826001369 m1A Human chr16 + 68230848 68230847 68230849 TGATATTCTCTTAGCTGCAGGGTACCTTGGGTAGTAGGCTGTGTAGTTCAGGTAGAGTTGAGTGG TGATATTCTCTTAGCTGCAGGGTACCTTGGGT__TAGGCTGTGTAGTTCAGGTAGAGTTGAGTGG TAG T L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:68230842..68230966 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 BLCA 1 - Human_RBP_ID_23696611 112893 RMVar_ID_112893 Human_SNP_ID_826001698 m1A Human chr16 - 30655153 30655153 30655153 GGATGCCGTGGACGAGCAAGATGTGGTGAGAGAAGGGGAGGCTCCCACTCCTCCGAGAGGGAAGA GGATGCCGTGGACGAGCAAGATGTGGTGAGAGCAGGGGAGGCTCCCACTCCTCCGAGAGGGAAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30654856..30655160 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112894 RMVar_ID_112894 Human_SNP_ID_826005123 m1A Human chr16 - 1367724 1367724 1367724 CAAGTCCAAACGGAGCTGAGCTGGCCCGGGTCAGGCGGCAGCTGGACGAGGCCAAGAGGAAGATC CAAGTCCAAACGGAGCTGAGCTGGCCCGGGTCGGGCGGCAGCTGGACGAGGCCAAGAGGAAGATC T C UNKL Ensembl:ENSG00000059145 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:1367163..1367804 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_8427858,Human_RBP_ID_18984950,Human_RBP_ID_22944947,Human_RBP_ID_23678972 Human_Splice_Rec_1659023,Human_Splice_Rec_1659051,Human_Splice_Rec_1659061,Human_Splice_Rec_1659073,Human_Splice_Rec_1659083,Human_Splice_Rec_1659111,Human_Splice_Rec_1659115,Human_Splice_Rec_1659125 112895 RMVar_ID_112895 Human_SNP_ID_826013820 m1A Human chr16 + 30711871 30711871 30711871 TGTGGAGGACCGGAGTGAGGATGAGGAAGATGAACATTCAGAGGAGGAAGAAACAAGTGGAAGTT TGTGGAGGACCGGAGTGAGGATGAGGAAGATGGACATTCAGAGGAGGAAGAAACAAGTGGAAGTT A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30711646..30712094 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_43838,Human_RBP_ID_1516819,Human_RBP_ID_1841470,Human_RBP_ID_2473177,Human_RBP_ID_3947585,Human_RBP_ID_5524342,Human_RBP_ID_5571692,Human_RBP_ID_6508187,Human_RBP_ID_8252088,Human_RBP_ID_8807036,Human_RBP_ID_9345632,Human_RBP_ID_9372662,Human_RBP_ID_12719817,Human_RBP_ID_18437542,Human_RBP_ID_18529754,Human_RBP_ID_18677780,Human_RBP_ID_20114660,Human_RBP_ID_22801121,Human_RBP_ID_22944636,Human_RBP_ID_23686802,Human_RBP_ID_24544512,Human_RBP_ID_26328902,Human_RBP_ID_27811046 Human_Splice_Rec_1703684,Human_Splice_Rec_1703742,Human_Splice_Rec_1703792,Human_Splice_Rec_1703836 RMVar_hsa_circ_99616,RMVar_hsa_circ_107259,RMVar_hsa_circ_269023,RMVar_hsa_circ_177921,RMVar_hsa_circ_177922,RMVar_hsa_circ_318517,RMVar_hsa_circ_356530,RMVar_hsa_circ_120311,RMVar_hsa_circ_117166,RMVar_hsa_circ_109887,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_99914,RMVar_hsa_circ_177924,RMVar_hsa_circ_177928,RMVar_hsa_circ_57072,RMVar_hsa_circ_177929,RMVar_hsa_circ_177926,RMVar_hsa_circ_177927,RMVar_hsa_circ_177925,RMVar_hsa_circ_177937,RMVar_hsa_circ_89434,RMVar_hsa_circ_374027,RMVar_hsa_circ_177923,RMVar_hsa_circ_69571,RMVar_hsa_circ_177936,RMVar_hsa_circ_351892,RMVar_hsa_circ_97114,RMVar_hsa_circ_80443,RMVar_hsa_circ_96560,RMVar_hsa_circ_177939,RMVar_hsa_circ_120667,RMVar_hsa_circ_177940,RMVar_hsa_circ_117833,RMVar_hsa_circ_177941,RMVar_hsa_circ_177942,RMVar_hsa_circ_177944 112896 RMVar_ID_112896 Human_SNP_ID_826019506 m1A Human chr16 + 29991145 29991145 29991145 CAGGCCCGTGAGATCGAGGCCTTCGATGCGGAAAGCATGAGGCTGGGCTTCTCCAGCATGGCTCT CAGGCCCGTGAGATCGAGGCCTTCGATGCGGAGAGCATGAGGCTGGGCTTCTCCAGCATGGCTCT A G TAOK2 Ensembl:ENSG00000149930 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:29991095..29991191 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_Splice_Rec_1700864,Human_Splice_Rec_1700884 RMVar_hsa_circ_107373,RMVar_hsa_circ_177807 112897 RMVar_ID_112897 Human_SNP_ID_826024335 m1A Human chr16 - 88717177 88717174 88717177 ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGAAGATCGTCAAGTACGGCATGGGTGGCCTCATCA ATACCCGCAGCCCAAAGGGCAGAAGAAGAAGA___TCGTCAAGTACGGCATGGGTGGCCTCATCA ATCT A PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88717002..88717407 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..35 33 COCA 1 - Human_RBP_ID_2489511,Human_RBP_ID_24544554,Human_RBP_ID_24558694,Human_RBP_ID_25241022 Human_Splice_Rec_1749790,Human_Splice_Rec_1749808,Human_Splice_Rec_1749842,Human_Splice_Rec_1749868 RMVar_hsa_circ_93984,RMVar_hsa_circ_80974,RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_180531,RMVar_hsa_circ_90544,RMVar_hsa_circ_180533,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_128141,RMVar_hsa_circ_180535,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_180540 112898 RMVar_ID_112898 Human_SNP_ID_826024858 m1A Human chr16 - 1999848 1999848 1999848 GGCGGCCCGGCCCTGCAGGAGCTTCTGAGCACACGCCCCACGGGCTCCGTCTCCTCCACACTGGG GGCGGCCCGGCCCTGCAGGAGCTTCTGAGCACGCGCCCCACGGGCTCCGTCTCCTCCACACTGGG T C ZNF598 Ensembl:ENSG00000167962 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12149722 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,rectum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,head and neck,large intestine Human_RBP_ID_6498226,Human_RBP_ID_27238139 RMVar_hsa_circ_118527,RMVar_hsa_circ_82495,RMVar_hsa_circ_175611,RMVar_hsa_circ_340653,RMVar_hsa_circ_175612 112899 RMVar_ID_112899 Human_SNP_ID_826029092 m1A Human chr16 + 29806672 29806672 29806672 CCCCGCGCGGCCCGCGCCCCCGGCCCCCGCTGAGCCCCGGGGGCCCCGCTGCGGCCGAGGCCATG CCCCGCGCGGCCCGCGCCCCCGGCCCCCGCTGGGCCCCGGGGGCCCCGCTGCGGCCGAGGCCATG A G MAZ Ensembl:ENSG00000103495 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:29806446..29806715 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4361654,Human_RBP_ID_8431739 Human_miRNA_ID_677009 112900 RMVar_ID_112900 Human_SNP_ID_826029788 m1A Human chr16 - 30123130 30123130 30123130 AACCGAGGGGGTCGGCCCGGGGGTCCCGGGGGAGGTGGAGATGGTGAAGGGGCAGCCGTTCGACG AACCGAGGGGGTCGGCCCGGGGGTCCCGGGGGGGGTGGAGATGGTGAAGGGGCAGCCGTTCGACG T C MAPK3 Ensembl:ENSG00000102882 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30123041..30123201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5754,Human_RBP_ID_233306,Human_RBP_ID_816965,Human_RBP_ID_888657,Human_RBP_ID_3947567,Human_RBP_ID_4362847,Human_RBP_ID_5113916,Human_RBP_ID_5141887,Human_RBP_ID_9419798,Human_RBP_ID_18419386,Human_RBP_ID_21973059,Human_RBP_ID_22441968,Human_RBP_ID_22584106,Human_RBP_ID_22654120,Human_RBP_ID_26328882,Human_RBP_ID_26769122,Human_RBP_ID_27811034 Human_Splice_Rec_1702007,Human_Splice_Rec_1702023,Human_Splice_Rec_1702053,Human_Splice_Rec_1702067,Human_Splice_Rec_1702097,Human_Splice_Rec_1702109,Human_Splice_Rec_1702133,Human_Splice_Rec_1702145 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 112901 RMVar_ID_112901 Human_SNP_ID_826029871 m1A Human chr16 + 10769147 10769147 10769147 ATGTTCAGGACCAAGCAGTTACCGAGCGAGGCACTCACTGGGCAGCACATCCAGCCAGACCCGAC ATGTTCAGGACCAAGCAGTTACCGAGCGAGGCTCTCACTGGGCAGCACATCCAGCCAGACCCGAC A T NUBP1 Ensembl:ENSG00000103274 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:10769096..10769189 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney Human_RBP_ID_17653296 Human_miRNA_ID_1097101 RMVar_hsa_circ_176211 112902 RMVar_ID_112902 Human_SNP_ID_826031947 m1A Human chr16 + 88717139 88717139 88717139 GAGCAGTGGGAACCAGATGATGGCGATGAGGAAGAGGATGATGAGGCCACCCATGCCGTACTTGA GAGCAGTGGGAACCAGATGATGGCGATGAGGACGAGGATGATGAGGCCACCCATGCCGTACTTGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88717090..88717156 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 112903 RMVar_ID_112903 Human_SNP_ID_826033085 m1A Human chr16 - 89900755 89900754 89900755 GAACATGGTGAGCGCCTGCTGTATCAGGAGAGAGGCCTTCTGCCTGGCAGAGCTCTGCTCACACT GAACATGGTGAGCGCCTGCTGTATCAGGAGAG_GGCCTTCTGCCTGGCAGAGCTCTGCTCACACT CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89900638..89900808 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 COAD 1 - 112904 RMVar_ID_112904 Human_SNP_ID_826033779 m1A Human chr16 - 88534510 88534505 88534510 TCGGGGGGCAGTAGGGGCAGGCGGCGGCGGGCAGGCCGAGCGCGCCGGGCGGTGGCGCAGCGGGG TCGGGGGGCAGTAGGGGCAGGCGGCGGCGGGC_____GAGCGCGCCGGGCGGTGGCGCAGCGGGG CGGCCT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88534283..88534682 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..37 33 BRCA 1 - 112905 RMVar_ID_112905 Human_SNP_ID_826035310 m1A Human chr16 + 2165882 2165882 2165882 AGGCCAGGTCTCCTCCGTCCTCCCTCTAGACCAGAATGGAAACGACCTTCGGACCCGCCTTTTCA AGGCCAGGTCTCCTCCGTCCTCCCTCTAGACCGGAATGGAAACGACCTTCGGACCCGCCTTTTCA A G TRAF7 Ensembl:ENSG00000131653 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2165876..2165950 26863196 MeRIP-seq:(Medium) rs77497016 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_761294,Human_RBP_ID_5357410,Human_RBP_ID_5646745,Human_RBP_ID_9325776,Human_RBP_ID_22583588,Human_RBP_ID_26809852 Human_Splice_Rec_1664714,Human_Splice_Rec_1664715,Human_Splice_Rec_1664720,Human_Splice_Rec_1664721,Human_Splice_Rec_1664730,Human_Splice_Rec_1664731,Human_Splice_Rec_1664770,Human_Splice_Rec_1664771,Human_Splice_Rec_1664776,Human_Splice_Rec_1664777,Human_Splice_Rec_1664792,Human_Splice_Rec_1664793 Human_miRNA_ID_2728071 RMVar_hsa_circ_888,RMVar_hsa_circ_46109,RMVar_hsa_circ_87998,RMVar_hsa_circ_90242,RMVar_hsa_circ_115814,RMVar_hsa_circ_20899,RMVar_hsa_circ_175695,RMVar_hsa_circ_124813,RMVar_hsa_circ_105643,RMVar_hsa_circ_175696,RMVar_hsa_circ_175698,RMVar_hsa_circ_175699,RMVar_hsa_circ_175697 112906 RMVar_ID_112906 Human_SNP_ID_826044725 m1A Human chr16 - 88805513 88805513 88805513 GCGGAACATCTCCGCCAGCACCTGGTACTTGTAGGGCAGCACGAGTCCCGGCAGGCCGGGCTGGG GCGGAACATCTCCGCCAGCACCTGGTACTTGTGGGGCAGCACGAGTCCCGGCAGGCCGGGCTGGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88803851..88808511 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 112907 RMVar_ID_112907 Human_SNP_ID_826050685 m1A Human chr16 + 8859322 8859322 8859322 GGTGGGGGGCTGTGGTGGTGGGGGAGGCTCAGATGACATGGCTGACCTGGAAAGAGAAGAGGCTG GGTGGGGGGCTGTGGTGGTGGGGGAGGCTCAGGTGACATGGCTGACCTGGAAAGAGAAGAGGCTG A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:8859176..8859350 26863196 MeRIP-seq:(Medium) rs1567184839 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 10 oesophagus Human_RBP_ID_3506925,Human_RBP_ID_5573648,Human_RBP_ID_8188818,Human_RBP_ID_12853816,Human_RBP_ID_22355947,Human_RBP_ID_22713017 112908 RMVar_ID_112908 Human_SNP_ID_826054767 m1A Human chr16 - 3729225 3729225 3729225 CACCACGGTGTCCACAGGGAAGCCTACCAGCCAGGTGCCGGCCCCCCCACCCCCGGCCCAGCCCC CACCACGGTGTCCACAGGGAAGCCTACCAGCCTGGTGCCGGCCCCCCCACCCCCGGCCCAGCCCC T A CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:3729176..3729388 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_27241960 RMVar_hsa_circ_268634 112909 RMVar_ID_112909 Human_SNP_ID_826057751 m1A Human chr16 - 70664908 70664908 70664908 CCTGCCACCATCGCAGCCAAGGTAGGCTGGCCAGGGCCCCCCTTCACGCCCAGGTCAGTCCCAGG CCTGCCACCATCGCAGCCAAGGTAGGCTGGCCGGGGCCCCCCTTCACGCCCAGGTCAGTCCCAGG T C MTSS2 Ensembl:ENSG00000132613 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70664901..70665017 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19072036 RMVar_hsa_circ_115261,RMVar_hsa_circ_179710,RMVar_hsa_circ_123812,RMVar_hsa_circ_179708 112910 RMVar_ID_112910 Human_SNP_ID_826062485 m1A Human chr16 - 11915672 11915672 11915672 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGAGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGGGGCAGCAGCGGCAGCAGCAGCAGCGACTCGGCG T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:11915570..11915690 26863410 MeRIP-seq:(Medium) rs1189427317 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_233475,Human_RBP_ID_5648359,Human_RBP_ID_9324949,Human_RBP_ID_17373827,Human_RBP_ID_17488832,Human_RBP_ID_17669772,Human_RBP_ID_18409386,Human_RBP_ID_22441787,Human_RBP_ID_22532676,Human_RBP_ID_22760640,Human_RBP_ID_24544754 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 112911 RMVar_ID_112911 Human_SNP_ID_826066755 m1A Human chr16 - 11742716 11742716 11742716 GGCGACTGGGAGCATGTAATGTCGGAATGCGGAGGCCGCGGCGGCGGCAGCAGCAGCAGCGAGGA GGCGACTGGGAGCATGTAATGTCGGAATGCGGGGGCCGCGGCGGCGGCAGCAGCAGCAGCGAGGA T C TXNDC11 Ensembl:ENSG00000153066 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr16:11742676..11742750;chr16:11742478..11742866 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus Human_RBP_ID_4393609,Human_RBP_ID_12664532,Human_RBP_ID_18418668,Human_RBP_ID_22441298 112912 RMVar_ID_112912 Human_SNP_ID_826068736 m1A Human chr16 - 89284965 89284965 89284965 CAGCTCCCTCTCTGCCTCCTCCACCTCGTCTCACGGGAGCTCTGCCGCCCAGAAGCAGAACCCCA CAGCTCCCTCTCTGCCTCCTCCACCTCGTCTCGCGGGAGCTCTGCCGCCCAGAAGCAGAACCCCA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89284653..89285104 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_45252,Human_RBP_ID_5465615,Human_RBP_ID_8442262,Human_RBP_ID_8811225,Human_RBP_ID_9286013,Human_RBP_ID_9373389,Human_RBP_ID_22054362,Human_RBP_ID_22713835,Human_RBP_ID_24544654,Human_RBP_ID_26330405,Human_RBP_ID_27447363,Human_RBP_ID_27572730,Human_RBP_ID_27812069 Human_miRNA_ID_1157592 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 112913 RMVar_ID_112913 Human_SNP_ID_826072259 m1A Human chr16 + 56477114 56477114 56477114 TTGTGCCACTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAAAAAAAAGAAGA TTGTGCCACTGCACTCCAGCCTGGGCAACAAGGGTGAAACTCTGTCTCAAAAAAAAAAAAGAAGA A G OGFOD1 Ensembl:ENSG00000087263 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112162270 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_126136 GWAS_ID_12545,GWAS_ID_12546,GWAS_ID_12547,GWAS_ID_12548,GWAS_ID_12549,GWAS_ID_12550,GWAS_ID_12551,GWAS_ID_12552,GWAS_ID_12553,GWAS_ID_12554,GWAS_ID_12555,GWAS_ID_12556,GWAS_ID_12557,GWAS_ID_12558,GWAS_ID_12559,GWAS_ID_12560,GWAS_ID_12561,GWAS_ID_12562,GWAS_ID_12563,GWAS_ID_12564,GWAS_ID_12565,GWAS_ID_12566,GWAS_ID_12567,GWAS_ID_12568,GWAS_ID_12569,GWAS_ID_12570,GWAS_ID_12571,GWAS_ID_12572,GWAS_ID_12573,GWAS_ID_12574,GWAS_ID_12575 RMVar_hsa_circ_178551,RMVar_hsa_circ_98818,RMVar_hsa_circ_114582,RMVar_hsa_circ_112805,RMVar_hsa_circ_110916,RMVar_hsa_circ_178557,RMVar_hsa_circ_178558,RMVar_hsa_circ_178561,RMVar_hsa_circ_105393,RMVar_hsa_circ_104978,RMVar_hsa_circ_178562,RMVar_hsa_circ_178563 112914 RMVar_ID_112914 Human_SNP_ID_826075791 m1A Human chr16 + 23570949 23570948 23570950 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTTT__AAAAAAAAAAAGCAGTTTCAATTGAAATATT TAA T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 33..34 33 UCEC 1 - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 112915 RMVar_ID_112915 Human_SNP_ID_826078935 m1A Human chr16 + 75568040 75568040 75568040 ACAGTCCTGACCTCTCTTTACTTTCCCAGGTGATTGTGGAAAAGGTCTCAGGCTCTCAGATTGTT ACAGTCCTGACCTCTCTTTACTTTCCCAGGTGCTTGTGGAAAAGGTCTCAGGCTCTCAGATTGTT A C GABARAPL2 Ensembl:ENSG00000034713 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75568026..75568075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_895647,Human_RBP_ID_4395362,Human_RBP_ID_8941513,Human_RBP_ID_22442647,Human_RBP_ID_23700674,Human_RBP_ID_26949558 Human_Splice_Rec_1741200,Human_Splice_Rec_1741204,Human_Splice_Rec_1741214 Human_miRNA_ID_3079966 RMVar_hsa_circ_78784,RMVar_hsa_circ_94628,RMVar_hsa_circ_180073,RMVar_hsa_circ_180074 112916 RMVar_ID_112916 Human_SNP_ID_826080106 m1A Human chr16 + 2766142 2766142 2766142 GGAAACGCTCTAGATCTCGAGCCTCTCCAGCCACTCACCGGCGATCCAGGTCCAGAACCCCCCTG GGAAACGCTCTAGATCTCGAGCCTCTCCAGCCTCTCACCGGCGATCCAGGTCCAGAACCCCCCTG A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2766009..2766400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_45339,Human_RBP_ID_1177602,Human_RBP_ID_1515654,Human_RBP_ID_1840782,Human_RBP_ID_3493718,Human_RBP_ID_8431171,Human_RBP_ID_8806494,Human_RBP_ID_12709738,Human_RBP_ID_17253719,Human_RBP_ID_17369370,Human_RBP_ID_17485915,Human_RBP_ID_18676607,Human_RBP_ID_27440837 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 112917 RMVar_ID_112917 Human_SNP_ID_826080315 m1A Human chr16 - 89561052 89561052 89561052 AGCCCCGAGCGCAGGGCTCACCTGCGGATCTTACGGGCCGGCTGGTTGAACCACGTGGCCACGCG AGCCCCGAGCGCAGGGCTCACCTGCGGATCTTCCGGGCCGGCTGGTTGAACCACGTGGCCACGCG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89561001..89561075 32194978 MeRIP-seq:(Medium) rs2280370 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,oesophagus squamous_cell_carcinoma 13 oesophagus,head and neck 112918 RMVar_ID_112918 Human_SNP_ID_826082864 m1A Human chr16 + 23570949 23570949 23570949 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTTAAAAAAAAAAAAGCAGTTTCAATTGAAATATT A T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs77282410 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 112919 RMVar_ID_112919 Human_SNP_ID_826083917 m1A Human chr16 + 24777086 24777086 24777086 ACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCAGCAGCAGCCACAGCAGCAGCCACAGCCGCAGC ACAGCAGCAGCAGCAACAGCAGCAGCCGCAGCCGCAGCAGCCACAGCAGCAGCCACAGCCGCAGC A C TNRC6A Ensembl:ENSG00000090905 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:24777037..24777162 26863196 MeRIP-seq:(Medium) rs1443272995 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22582274 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725,RMVar_hsa_circ_107442,RMVar_hsa_circ_75510,RMVar_hsa_circ_297699,RMVar_hsa_circ_353789,RMVar_hsa_circ_277356,RMVar_hsa_circ_177405,RMVar_hsa_circ_177406,RMVar_hsa_circ_292740,RMVar_hsa_circ_339498,RMVar_hsa_circ_350948,RMVar_hsa_circ_374809,RMVar_hsa_circ_294392,RMVar_hsa_circ_265374,RMVar_hsa_circ_177412,RMVar_hsa_circ_71651,RMVar_hsa_circ_92436,RMVar_hsa_circ_45427,RMVar_hsa_circ_177413,RMVar_hsa_circ_177410,RMVar_hsa_circ_177411,RMVar_hsa_circ_177409 112920 RMVar_ID_112920 Human_SNP_ID_826085123 m1A Human chr16 - 23603337 23603337 23603337 GACACTTAAAATGATTGCTTGTTTATGTCCAGACAGACTTATTTTTTATTCTAATGATGGTAGCA GACACTTAAAATGATTGCTTGTTTATGTCCAGCCAGACTTATTTTTTATTCTAATGATGGTAGCA T G PALB2 Ensembl:ENSG00000083093 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:23603286..23603381 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_6501788,Human_RBP_ID_17253460,Human_RBP_ID_17485655,Human_RBP_ID_18284898,Human_RBP_ID_27657481 Human_miRNA_ID_1546589 RMVar_hsa_circ_177334,RMVar_hsa_circ_126804 112921 RMVar_ID_112921 Human_SNP_ID_826101233 m1A Human chr16 - 67909198 67909198 67909198 CCTCCACCAGCTGGATGATGTTGGCATGACGCACCCGACGCAGCACACGCAGCTCCGACTCACAC CCTCCACCAGCTGGATGATGTTGGCATGACGCGCCCGACGCAGCACACGCAGCTCCGACTCACAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:67909147..67909238 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 112922 RMVar_ID_112922 Human_SNP_ID_826112018 m1A Human chr16 + 1314364 1314364 1314364 ATGAACCTCATGAACTGGGAGTGCGCCATTCCAGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT ATGAACCTCATGAACTGGGAGTGCGCCATTCCCGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT A C UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1314253..1314414 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 8 lung Human_RBP_ID_468382,Human_RBP_ID_1512459,Human_RBP_ID_8427778,Human_RBP_ID_12668039,Human_RBP_ID_19070395,Human_RBP_ID_26809801 Human_Splice_Rec_1658214,Human_Splice_Rec_1658215,Human_Splice_Rec_1658226,Human_Splice_Rec_1658227,Human_Splice_Rec_1658240,Human_Splice_Rec_1658241,Human_Splice_Rec_1658252,Human_Splice_Rec_1658253,Human_Splice_Rec_1658258,Human_Splice_Rec_1658259,Human_Splice_Rec_1658268,Human_Splice_Rec_1658269,Human_Splice_Rec_1658282,Human_Splice_Rec_1658288,Human_Splice_Rec_1658289,Human_Splice_Rec_1658306,Human_Splice_Rec_1658310,Human_Splice_Rec_1658311,Human_Splice_Rec_1658322,Human_Splice_Rec_1658323,Human_Splice_Rec_1658334,Human_Splice_Rec_1658335,Human_Splice_Rec_1658342,Human_Splice_Rec_1658343,Human_Splice_Rec_1658350,Human_Splice_Rec_1658351 RMVar_hsa_circ_27192,RMVar_hsa_circ_319499,RMVar_hsa_circ_337966,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_25213,RMVar_hsa_circ_175474,RMVar_hsa_circ_175472,RMVar_hsa_circ_343464 112923 RMVar_ID_112923 Human_SNP_ID_826112021 m1A Human chr16 + 1314364 1314364 1314364 ATGAACCTCATGAACTGGGAGTGCGCCATTCCAGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT ATGAACCTCATGAACTGGGAGTGCGCCATTCCGGGAAAGAAAGGGGTAAGGGGCGCTGCCGGCCT A G UBE2I Ensembl:ENSG00000103275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1314253..1314414 26863196 MeRIP-seq:(Medium) rs4610 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,pancreas ductal_carcinoma,COCA,large_intestine adenocarcinoma 17 pancreas,large intestine Human_RBP_ID_468382,Human_RBP_ID_1512459,Human_RBP_ID_8427778,Human_RBP_ID_12668039,Human_RBP_ID_19070395,Human_RBP_ID_26809801 Human_Splice_Rec_1658214,Human_Splice_Rec_1658215,Human_Splice_Rec_1658226,Human_Splice_Rec_1658227,Human_Splice_Rec_1658240,Human_Splice_Rec_1658241,Human_Splice_Rec_1658252,Human_Splice_Rec_1658253,Human_Splice_Rec_1658258,Human_Splice_Rec_1658259,Human_Splice_Rec_1658268,Human_Splice_Rec_1658269,Human_Splice_Rec_1658282,Human_Splice_Rec_1658288,Human_Splice_Rec_1658289,Human_Splice_Rec_1658306,Human_Splice_Rec_1658310,Human_Splice_Rec_1658311,Human_Splice_Rec_1658322,Human_Splice_Rec_1658323,Human_Splice_Rec_1658334,Human_Splice_Rec_1658335,Human_Splice_Rec_1658342,Human_Splice_Rec_1658343,Human_Splice_Rec_1658350,Human_Splice_Rec_1658351 GWAS_ID_8861 RMVar_hsa_circ_27192,RMVar_hsa_circ_319499,RMVar_hsa_circ_337966,RMVar_hsa_circ_284495,RMVar_hsa_circ_175473,RMVar_hsa_circ_25213,RMVar_hsa_circ_175474,RMVar_hsa_circ_175472,RMVar_hsa_circ_343464 112924 RMVar_ID_112924 Human_SNP_ID_826112891 m1A Human chr16 - 2975746 2975746 2975746 TAAAGCGTTCCATGTCACCATTCCGGGGCCCCAAGGACCGGGCCCGCAAGTTGGCCGAGGTGGGC TAAAGCGTTCCATGTCACCATTCCGGGGCCCCCAGGACCGGGCCCGCAAGTTGGCCGAGGTGGGC T G PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:2975569..2975825;chr16:2975510..2975826 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_5113841,Human_RBP_ID_17875272,Human_RBP_ID_18418645,Human_RBP_ID_21972270,Human_RBP_ID_22800988,Human_RBP_ID_22944969,Human_RBP_ID_24476111,Human_RBP_ID_26328046,Human_RBP_ID_26942724 Human_Splice_Rec_1667816,Human_Splice_Rec_1667836,Human_Splice_Rec_1667856,Human_Splice_Rec_1667882,Human_Splice_Rec_1667898,Human_Splice_Rec_1667914,Human_Splice_Rec_1667928,Human_Splice_Rec_1667944,Human_Splice_Rec_1667952,Human_Splice_Rec_1667958,Human_Splice_Rec_1667964 112925 RMVar_ID_112925 Human_SNP_ID_826114744 m1A Human chr16 + 46730691 46730691 46730691 ACCCGGTGTTCAAAAGGAGCTGGTGGGGCCGGACTGTCATCTGCTCAGGAGGCAATAAGGACCTG ACCCGGTGTTCAAAAGGAGCTGGTGGGGCCGGGCTGTCATCTGCTCAGGAGGCAATAAGGACCTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:46730661..46730734 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 112926 RMVar_ID_112926 Human_SNP_ID_826116710 m1A Human chr16 + 14644343 14644343 14644343 TTTTTTATGTCTCTGGAACCCAGAATTTGCTAAGAGATGGAGGAACCTCAGAAAAGCTATGTGAA TTTTTTATGTCTCTGGAACCCAGAATTTGCTAGGAGATGGAGGAACCTCAGAAAAGCTATGTGAA A G BFAR Ensembl:ENSG00000103429 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:14644292..14644441 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_468604,Human_RBP_ID_1002960,Human_RBP_ID_1512657,Human_RBP_ID_1838322,Human_RBP_ID_4351164,Human_RBP_ID_5142174,Human_RBP_ID_6494843,Human_RBP_ID_12671262,Human_RBP_ID_17689648,Human_RBP_ID_18673417,Human_RBP_ID_27237188 Human_Splice_Rec_1680488,Human_Splice_Rec_1680492,Human_Splice_Rec_1680502,Human_Splice_Rec_1680508,Human_Splice_Rec_1680514,Human_Splice_Rec_1680528 RMVar_hsa_circ_176462,RMVar_hsa_circ_300697,RMVar_hsa_circ_176459,RMVar_hsa_circ_97603,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_303805,RMVar_hsa_circ_79532,RMVar_hsa_circ_270302,RMVar_hsa_circ_176464,RMVar_hsa_circ_176465,RMVar_hsa_circ_176463,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461 112927 RMVar_ID_112927 Human_SNP_ID_826124088 m1A Human chr16 - 23510429 23510429 23510429 GCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGAGCGATGGCGGCGACCGCG GCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCGGCGTCGGGGCTGGAGCGATGGCGGCGACCGCG T C GGA2 Ensembl:ENSG00000103365 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:23510274..23510500 26863196 MeRIP-seq:(Medium) rs2285522 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_234750,Human_RBP_ID_4392912,Human_RBP_ID_9374038,Human_RBP_ID_18418961,Human_RBP_ID_18985748 112928 RMVar_ID_112928 Human_SNP_ID_826126753 m1A Human chr16 + 15127847 15127847 15127847 GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCACTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC GGAGAGCCAGATGTGCTTGTCAAAGAAGCCGCGCTGCAGCTCAGCCACCAGCAGGCGCCGGAAGC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15127789..15128318 32194978 MeRIP-seq:(Medium) rs545460151 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_100749,RMVar_hsa_circ_176478,RMVar_hsa_circ_106248,RMVar_hsa_circ_176479,RMVar_hsa_circ_99598,RMVar_hsa_circ_107062,RMVar_hsa_circ_176487,RMVar_hsa_circ_176488 112929 RMVar_ID_112929 Human_SNP_ID_826137592 m1A Human chr16 - 1351787 1351787 1351787 CCCCAGGTCCGCGCCATGGGCCGCAGGAGGGCAGCGCGCGGGCCGGGGGCGGAAGGCGGCCGCCC CCCCAGGTCCGCGCCATGGGCCGCAGGAGGGCTGCGCGCGGGCCGGGGGCGGAAGGCGGCCGCCC T A TSR3 Ensembl:ENSG00000007520 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr16:1351711..1351812 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver Human_RBP_ID_4392733,Human_RBP_ID_9353085 Human_Splice_Rec_1658905 112930 RMVar_ID_112930 Human_SNP_ID_826147886 m1A Human chr16 - 4847188 4847188 4847188 CGAGCGGCCGGGCCAACCGAGACGCGCCGGGGAGCTACCCGCCTGGGCGCGGGGTTCGCTGCCGG CGAGCGGCCGGGCCAACCGAGACGCGCCGGGGGGCTACCCGCCTGGGCGCGGGGTTCGCTGCCGG T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4847185..4847255 26863196 MeRIP-seq:(Medium) rs1341116798 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_889425,Human_RBP_ID_26780174 112931 RMVar_ID_112931 Human_SNP_ID_826157031 m1A Human chr16 - 17259215 17259215 17259215 TCCCGGGGACAGAGCCGCAGCCAACAGCAGCCACGGGAAGGATGTGTCCAGACCGCCTCATGCCA TCCCGGGGACAGAGCCGCAGCCAACAGCAGCCTCGGGAAGGATGTGTCCAGACCGCCTCATGCCA T A XYLT1 Ensembl:ENSG00000103489 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:17259167..17259290 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine RMVar_hsa_circ_89489,RMVar_hsa_circ_125384,RMVar_hsa_circ_176735,RMVar_hsa_circ_176737,RMVar_hsa_circ_120133,RMVar_hsa_circ_176742,RMVar_hsa_circ_371206,RMVar_hsa_circ_176743,RMVar_hsa_circ_27004,RMVar_hsa_circ_176746,RMVar_hsa_circ_276677,RMVar_hsa_circ_322449,RMVar_hsa_circ_176747 112932 RMVar_ID_112932 Human_SNP_ID_826170594 m1A Human chr16 + 81710898 81710898 81710898 TGCTGTCCCCTGTCCCCAACGGAGACTCTGTCACCCCTGGGCTCCCCCTGCCATCGTGTGCTTCA TGCTGTCCCCTGTCCCCAACGGAGACTCTGTCCCCCCTGGGCTCCCCCTGCCATCGTGTGCTTCA A C CMIP Ensembl:ENSG00000153815 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:81710847..81710975 26863196 MeRIP-seq:(Medium) rs989086764 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_480283,Human_RBP_ID_8186001,Human_RBP_ID_8440075,Human_RBP_ID_17077965,Human_RBP_ID_17371535,Human_RBP_ID_18939496,Human_RBP_ID_26445431 Human_miRNA_ID_1709648,Human_miRNA_ID_2877917 RMVar_hsa_circ_124545,RMVar_hsa_circ_180195 112933 RMVar_ID_112933 Human_SNP_ID_826172717 m1A Human chr16 + 46903964 46903964 46903964 AGAGCTTAAGGGGAAACGTGGCATTCACGCTCATGGGGAGGATGAGTAAGAACCTGCAAATGCAT AGAGCTTAAGGGGAAACGTGGCATTCACGCTCTTGGGGAGGATGAGTAAGAACCTGCAAATGCAT A T GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:46903962..46904064 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_12740448,Human_RBP_ID_23689784 RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_287310,RMVar_hsa_circ_326819,RMVar_hsa_circ_373404,RMVar_hsa_circ_178112,RMVar_hsa_circ_178114,RMVar_hsa_circ_344182,RMVar_hsa_circ_332278 112934 RMVar_ID_112934 Human_SNP_ID_826175117 m1A Human chr16 + 31120426 31120426 31120426 AGTGAAGGATGCTGTACAGAAGAACTCAGAGAAGTACCTGAGCGAGCTCGCAGAGCAGCCTGAGC AGTGAAGGATGCTGTACAGAAGAACTCAGAGAGGTACCTGAGCGAGCTCGCAGAGCAGCCTGAGC A G KAT8 Ensembl:ENSG00000103510 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31120376..31120450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney Human_RBP_ID_892037,Human_RBP_ID_1517265,Human_RBP_ID_1841764,Human_RBP_ID_8432710,Human_RBP_ID_12723922,Human_RBP_ID_18986195 Human_Splice_Rec_1705126,Human_Splice_Rec_1705127,Human_Splice_Rec_1705146,Human_Splice_Rec_1705147,Human_Splice_Rec_1705164,Human_Splice_Rec_1705165,Human_Splice_Rec_1705184 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_64374,RMVar_hsa_circ_274125,RMVar_hsa_circ_178015,RMVar_hsa_circ_178016 112935 RMVar_ID_112935 Human_SNP_ID_826183072 m1A Human chr16 - 70664649 70664649 70664649 GCCGGGACTCGCTGCAGTACTCCAGCGGCTACAGCACGCAGACCACCACGCCCTCCTGCTCTGAG GCCGGGACTCGCTGCAGTACTCCAGCGGCTACGGCACGCAGACCACCACGCCCTCCTGCTCTGAG T C MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:70664598..70664725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_126675 RMVar_hsa_circ_115261,RMVar_hsa_circ_179710,RMVar_hsa_circ_123812,RMVar_hsa_circ_179708,RMVar_hsa_circ_120539,RMVar_hsa_circ_179709 112936 RMVar_ID_112936 Human_SNP_ID_826183629 m1A Human chr16 - 3611814 3611814 3611814 TCACAGCTGCCACAGTGCCTTAAACTCGCCCTAACTCTTTCTCAAAAACTAACAGACTCCACCTG TCACAGCTGCCACAGTGCCTTAAACTCGCCCTGACTCTTTCTCAAAAACTAACAGACTCCACCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3611763..3612040 26863196 MeRIP-seq:(Medium) rs12924990 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_8895,GWAS_ID_8896,GWAS_ID_8897,GWAS_ID_8898,GWAS_ID_8899,GWAS_ID_8900,GWAS_ID_8901 112937 RMVar_ID_112937 Human_SNP_ID_826189957 m1A Human chr16 - 4316181 4316181 4316181 GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGAGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG GCGGTCGGGGGGCGCGGGGAGCCGAGCGGGGGGGGGGCCGGGACGGGCGGGGGCCGGGGCGCGAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:4316086..4316227 26863410 MeRIP-seq:(Medium) rs1004465055 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112938 RMVar_ID_112938 Human_SNP_ID_826191761 m1A Human chr16 + 11851497 11851497 11851497 TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGAGGCCGAATCCTCCATCTTGTTTCCACCTCGTG TCCAGTAGCGGCTGCAGAAGACAGCGAGGCCGTGGCCGAATCCTCCATCTTGTTTCCACCTCGTG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:11851451..11851550;chr16:11851451..11851525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 112939 RMVar_ID_112939 Human_SNP_ID_826199627 m1A Human chr16 + 69324848 69324848 69324848 GCCTCAAAGACCGAGTGACATAAGCCATTCCCACCCTCCTAGGTTCACATCCAGGGCTGTGTCTT GCCTCAAAGACCGAGTGACATAAGCCATTCCCCCCCTCCTAGGTTCACATCCAGGGCTGTGTCTT A C VPS4A Ensembl:ENSG00000132612 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69324800..69324950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_478326,Human_RBP_ID_1366249,Human_RBP_ID_5114306,Human_RBP_ID_8437390,Human_RBP_ID_26445280 Human_miRNA_ID_1702701 RMVar_hsa_circ_95764,RMVar_hsa_circ_179381,RMVar_hsa_circ_84005,RMVar_hsa_circ_76611,RMVar_hsa_circ_179386,RMVar_hsa_circ_88001,RMVar_hsa_circ_104486,RMVar_hsa_circ_179387,RMVar_hsa_circ_179388,RMVar_hsa_circ_102830,RMVar_hsa_circ_112937,RMVar_hsa_circ_179389,RMVar_hsa_circ_179390,RMVar_hsa_circ_107038,RMVar_hsa_circ_179391,RMVar_hsa_circ_94485,RMVar_hsa_circ_109539,RMVar_hsa_circ_123073,RMVar_hsa_circ_179392,RMVar_hsa_circ_179393,RMVar_hsa_circ_179394,RMVar_hsa_circ_179395 112940 RMVar_ID_112940 Human_SNP_ID_826200156 m1A Human chr16 + 87739327 87739327 87739327 ATCCACACACCAGCACCTCATCCATCCACACAACAGCATCTCATCCATCCACACACCAGCATCTC ATCCACACACCAGCACCTCATCCATCCACACACCAGCATCTCATCCATCCACACACCAGCATCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:87739281..87739505;chr16:87739280..87739518;chr16:87739258..87739528 26863196 MeRIP-seq:(Medium) rs868750821 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue 112941 RMVar_ID_112941 Human_SNP_ID_826208439 m1A Human chr16 - 346901 346901 346901 ACTGGTGTCCACAGACCCGAGGCCCGCCAGCTACAGTTTCTGCTCCGGGAAAGGTGTTGGCATTA ACTGGTGTCCACAGACCCGAGGCCCGCCAGCTGCAGTTTCTGCTCCGGGAAAGGTGTTGGCATTA T C AXIN1 Ensembl:ENSG00000103126 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:346851..346950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 4 biliary tract,gallbladder Human_RBP_ID_4392677,Human_RBP_ID_8433638,Human_RBP_ID_22054408,Human_RBP_ID_24370098 RMVar_hsa_circ_289861,RMVar_hsa_circ_175324,RMVar_hsa_circ_290683,RMVar_hsa_circ_175327,RMVar_hsa_circ_343941,RMVar_hsa_circ_175329,RMVar_hsa_circ_283255 112942 RMVar_ID_112942 Human_SNP_ID_826216999 m1A Human chr16 - 67663725 67663725 67663725 AGGCATTCCTGCTCACTGCAGGTCCTGGCACAAGTGCTAGAGCAGCAGCGGCAGGCCCAGGAGCA AGGCATTCCTGCTCACTGCAGGTCCTGGCACATGTGCTAGAGCAGCAGCGGCAGGCCCAGGAGCA T A ENKD1 Ensembl:ENSG00000124074 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:67663637..67663750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5288686,Human_RBP_ID_23696109 Human_Splice_Rec_1728668,Human_Splice_Rec_1728669,Human_Splice_Rec_1728674,Human_Splice_Rec_1728675,Human_Splice_Rec_1728692,Human_Splice_Rec_1728693,Human_Splice_Rec_1728702 RMVar_hsa_circ_97928,RMVar_hsa_circ_179111 112943 RMVar_ID_112943 Human_SNP_ID_826225781 m1A Human chr16 - 31492249 31492249 31492249 ACACATGGGCTGATGCTTGGGGCCCTGCAGGGAGATGGACCCCTTCCAGCAGAGCTGGAGGAGCT ACACATGGGCTGATGCTTGGGGCCCTGCAGGGGGATGGACCCCTTCCAGCAGAGCTGGAGGAGCT T C C16orf58 Ensembl:ENSG00000140688 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:31492090..31492285 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_818773,Human_RBP_ID_18986227,Human_RBP_ID_26330041,Human_RBP_ID_26446085 Human_Splice_Rec_1706382,Human_Splice_Rec_1706383,Human_Splice_Rec_1706406,Human_Splice_Rec_1706407,Human_Splice_Rec_1706412,Human_Splice_Rec_1706413,Human_Splice_Rec_1706436,Human_Splice_Rec_1706437,Human_Splice_Rec_1706462,Human_Splice_Rec_1706463 Human_miRNA_ID_2385485 RMVar_hsa_circ_11795,RMVar_hsa_circ_299524,RMVar_hsa_circ_59505,RMVar_hsa_circ_115697,RMVar_hsa_circ_116899,RMVar_hsa_circ_178056,RMVar_hsa_circ_178057 112944 RMVar_ID_112944 Human_SNP_ID_826227124 m1A Human chr16 + 28835973 28835973 28835973 CCAAACTGGAATCACAGCAGCCCCGCCCCCTCACCCTGGGGCTCCCCACCCGCCCCAGGTGATGC CCAAACTGGAATCACAGCAGCCCCGCCCCCTCCCCCTGGGGCTCCCCACCCGCCCCAGGTGATGC A C ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28835951..28836150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_235062,Human_RBP_ID_762839,Human_RBP_ID_17078647,Human_RBP_ID_17371381,Human_RBP_ID_22532782,Human_RBP_ID_24476011 Human_Splice_Rec_1697634,Human_Splice_Rec_1697676,Human_Splice_Rec_1697720,Human_Splice_Rec_1697764,Human_Splice_Rec_1697810,Human_Splice_Rec_1697852,Human_Splice_Rec_1697896,Human_Splice_Rec_1697940,Human_Splice_Rec_1698010,Human_Splice_Rec_1698050,Human_Splice_Rec_1698062,Human_Splice_Rec_1698076,Human_Splice_Rec_1698078,Human_Splice_Rec_1698084 Human_miRNA_ID_464664,Human_miRNA_ID_842524,Human_miRNA_ID_874312,Human_miRNA_ID_1232685,Human_miRNA_ID_1418602,Human_miRNA_ID_1559937 112945 RMVar_ID_112945 Human_SNP_ID_826228566 m1A Human chr16 + 25170780 25170780 25170780 CATCGGCCGTCGACATGATGGAGTTGTACAACAGGTTACCTCGAGCTGAAGTGAGCAGGTATGGG CATCGGCCGTCGACATGATGGAGTTGTACAACTGGTTACCTCGAGCTGAAGTGAGCAGGTATGGG A T LCMT1 Ensembl:ENSG00000205629 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:25170664..25170802 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_Splice_Rec_1693916,Human_Splice_Rec_1693917,Human_Splice_Rec_1693930,Human_Splice_Rec_1693931,Human_Splice_Rec_1693946,Human_Splice_Rec_1693947,Human_Splice_Rec_1693962,Human_Splice_Rec_1693963,Human_Splice_Rec_1693994,Human_Splice_Rec_1693995,Human_Splice_Rec_1694004,Human_Splice_Rec_1694005 Human_miRNA_ID_2477769 RMVar_hsa_circ_99021,RMVar_hsa_circ_177440,RMVar_hsa_circ_115718,RMVar_hsa_circ_68904,RMVar_hsa_circ_19296,RMVar_hsa_circ_177441,RMVar_hsa_circ_346317,RMVar_hsa_circ_52335,RMVar_hsa_circ_312672,RMVar_hsa_circ_119792,RMVar_hsa_circ_177447,RMVar_hsa_circ_177448,RMVar_hsa_circ_86148,RMVar_hsa_circ_177451,RMVar_hsa_circ_341896,RMVar_hsa_circ_277512,RMVar_hsa_circ_177450,RMVar_hsa_circ_177453,RMVar_hsa_circ_114759,RMVar_hsa_circ_320673,RMVar_hsa_circ_270356,RMVar_hsa_circ_177454,RMVar_hsa_circ_177452,RMVar_hsa_circ_282655,RMVar_hsa_circ_177455,RMVar_hsa_circ_177456,RMVar_hsa_circ_177457,RMVar_hsa_circ_290247 112946 RMVar_ID_112946 Human_SNP_ID_826238467 m1A Human chr16 - 798861 798861 798861 CAGGCAGGTGCAGCAGGAGGCCCTCGGGGGTCAGGTGCCACCACTCACCTGCCACCCGCCCACCC CAGGCAGGTGCAGCAGGAGGCCCTCGGGGGTCGGGTGCCACCACTCACCTGCCACCCGCCCACCC T C GNG13 Ensembl:ENSG00000127588 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:798835..798990;chr16:798834..798993 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112947 RMVar_ID_112947 Human_SNP_ID_826241870 m1A Human chr16 + 1972106 1972106 1972106 GTTCTGTGAAGAGTTCGGTGCTAACCTCCCTCACGCGGCGGTGGCTGCCGGGACCCTAGCAGGTT GTTCTGTGAAGAGTTCGGTGCTAACCTCCCTCGCGCGGCGGTGGCTGCCGGGACCCTAGCAGGTT A G TBL3 Ensembl:ENSG00000183751 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:1972051..1972229;chr16:1972051..1972365;chr16:1972051..1972528 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_4354527,Human_RBP_ID_23209222 Human_Splice_Rec_1661209,Human_Splice_Rec_1661251,Human_Splice_Rec_1661261,Human_Splice_Rec_1661301 112948 RMVar_ID_112948 Human_SNP_ID_826242902 m1A Human chr16 + 89282352 89282352 89282352 TGTTGTAAGAAACTCCGTAAGCATCCGCCTCCAGGAAGTCCTTTTCGTACTGGCCGGAGTCCTTC TGTTGTAAGAAACTCCGTAAGCATCCGCCTCCGGGAAGTCCTTTTCGTACTGGCCGGAGTCCTTC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:89282301..89282550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 3 stomach 112949 RMVar_ID_112949 Human_SNP_ID_826245603 m1A Human chr16 - 89282916 89282916 89282916 AGAGAAAGTCTTTGAAAAGCACAAGGAGAAGAAGGATAAAGAGTCCACAGAAAAGTACAAGGACA AGAGAAAGTCTTTGAAAAGCACAAGGAGAAGAGGGATAAAGAGTCCACAGAAAAGTACAAGGACA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:89282701..89283230 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_2489847,Human_RBP_ID_22003763 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 112950 RMVar_ID_112950 Human_SNP_ID_826251645 m1A Human chr16 + 636145 636145 636145 CCACGTCCGACGGCTGCCACTCGGCCAGGGGGAAGGCCCGCGCGAAGTGCGCTGCGTGCTGGCCG CCACGTCCGACGGCTGCCACTCGGCCAGGGGGGAGGCCCGCGCGAAGTGCGCTGCGTGCTGGCCG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:636076..636275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver 112951 RMVar_ID_112951 Human_SNP_ID_826257188 m1A Human chr16 + 8783005 8783005 8783005 CATCGACCTATTTTTGTTGAAGAATGAAAGGCAATGACAAGTTTAACATATACAAATTCGTGAAT CATCGACCTATTTTTGTTGAAGAATGAAAGGCGATGACAAGTTTAACATATACAAATTCGTGAAT A G ABAT Ensembl:ENSG00000183044 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs45615432 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Clinvar_Rec_330,Clinvar_Rec_331,Clinvar_Rec_332,Clinvar_Rec_333,Clinvar_Rec_334 GWAS_ID_8902,GWAS_ID_8903,GWAS_ID_8904,GWAS_ID_8905,GWAS_ID_8906,GWAS_ID_8907,GWAS_ID_8908 112952 RMVar_ID_112952 Human_SNP_ID_826258062 m1A Human chr16 - 69341318 69341318 69341318 AGTTCTGTAACAGCTACCATCTCTACTCACCAAAGGGATGTCTGCCATGGAGTACACCACCACGC AGTTCTGTAACAGCTACCATCTCTACTCACCACAGGGATGTCTGCCATGGAGTACACCACCACGC T G AC026464.3,AC026464.1 Ensembl:ENSG00000260371,Ensembl:ENSG00000259900 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69341200..69341350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_18682752 112953 RMVar_ID_112953 Human_SNP_ID_826268450 m1A Human chr16 + 30070263 30070263 30070263 TGCCCCCAACACTCCAGGCCCTGCCCCCTCCCACTCTTGAAGAGGAGGCCGCCTCCTCGGGGCTC TGCCCCCAACACTCCAGGCCCTGCCCCCTCCCGCTCTTGAAGAGGAGGCCGCCTCCTCGGGGCTC A G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding 3'UTR,3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:30070162..30070325 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 14 large intestine Human_RBP_ID_45005,Human_RBP_ID_233818,Human_RBP_ID_472462,Human_RBP_ID_4362657,Human_RBP_ID_8432006,Human_RBP_ID_18190006,Human_RBP_ID_20113487,Human_RBP_ID_22532812,Human_RBP_ID_24413108,Human_RBP_ID_26440720,Human_RBP_ID_26768896,Human_RBP_ID_26811277,Human_RBP_ID_26942617,Human_RBP_ID_27240289,Human_RBP_ID_27447938 RMVar_hsa_circ_104381,RMVar_hsa_circ_177816,RMVar_hsa_circ_96135,RMVar_hsa_circ_177820,RMVar_hsa_circ_116494,RMVar_hsa_circ_177824,RMVar_hsa_circ_114630,RMVar_hsa_circ_82249,RMVar_hsa_circ_177829,RMVar_hsa_circ_177830,RMVar_hsa_circ_92516,RMVar_hsa_circ_177831 112954 RMVar_ID_112954 Human_SNP_ID_826270481 m1A Human chr16 - 56362865 56362865 56362865 CTTCCTCAGCTGCCTCCTGCGCCCTGTGCCCGACTGACTGGAGGAGGCCTGTCCCAATTCTGCCC CTTCCTCAGCTGCCTCCTGCGCCCTGTGCCCGGCTGACTGGAGGAGGCCTGTCCCAATTCTGCCC T C AMFR Ensembl:ENSG00000159461 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:56362817..56362975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_475673,Human_RBP_ID_761687,Human_RBP_ID_894443,Human_RBP_ID_8187022,Human_RBP_ID_9325995,Human_RBP_ID_17653037,Human_RBP_ID_18680786,Human_RBP_ID_22441011,Human_RBP_ID_23692902,Human_RBP_ID_24370812,Human_RBP_ID_26441692,Human_RBP_ID_26810347 Human_miRNA_ID_642019 RMVar_hsa_circ_107159,RMVar_hsa_circ_117430,RMVar_hsa_circ_178520,RMVar_hsa_circ_178521 112955 RMVar_ID_112955 Human_SNP_ID_826271088 m1A Human chr16 - 4038833 4038833 4038833 GCCCGAGAGACATTCAGGGTTCAGGCAGTGGGAGTGGAAGGAAAGTAGTGGATTCCACAGCGAGA GCCCGAGAGACATTCAGGGTTCAGGCAGTGGGCGTGGAAGGAAAGTAGTGGATTCCACAGCGAGA T G ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:4038793..4038879 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 112956 RMVar_ID_112956 Human_SNP_ID_826285961 m1A Human chr16 + 72787719 72787698 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCG_____________________CCGCCGCCGCCGCCGCCACTGCCACCGCCGCC GCCGCCGCCGCCGCCGCCGCCA G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs781609559 Functional Loss DEL ICGC 13..33 33 ESCA 1 - Human_RBP_ID_9325207 112957 RMVar_ID_112957 Human_SNP_ID_826290101 m1A Human chr16 + 31180161 31180161 31180161 AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTACTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG AGGCGGGGCTGCTCAGTCCTCCAGGCGTCGGTGCTCAGCGGTGTTGGAACTTCGTTGCTTGCTTG A G FUS Ensembl:ENSG00000089280 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs929867 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 8 brain Human_RBP_ID_473397,Human_RBP_ID_763399,Human_RBP_ID_816457,Human_RBP_ID_1517294,Human_RBP_ID_1841782,Human_RBP_ID_4393799,Human_RBP_ID_5180679,Human_RBP_ID_5419257,Human_RBP_ID_5440470,Human_RBP_ID_5465893,Human_RBP_ID_8432726,Human_RBP_ID_9372734,Human_RBP_ID_18678318,Human_RBP_ID_22440986,Human_RBP_ID_26440974,Human_RBP_ID_26944095,Human_RBP_ID_27658010 Human_Splice_Rec_1705375,Human_Splice_Rec_1705401,Human_Splice_Rec_1705405,Human_Splice_Rec_1705433,Human_Splice_Rec_1705461,Human_Splice_Rec_1705485 Clinvar_Rec_445 112958 RMVar_ID_112958 Human_SNP_ID_826305430 m1A Human chr16 - 20734129 20734129 20734129 GGAAAGATTTTGATTATACAGTTTGTTTTTAAATTGTCTTTTATATTTATTTGTATTTGGTAAGA GGAAAGATTTTGATTATACAGTTTGTTTTTAAGTTGTCTTTTATATTTATTTGTATTTGGTAAGA T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058902 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_6498358,Human_RBP_ID_24475677,Human_RBP_ID_26939806 Human_miRNA_ID_852851 GWAS_ID_7941,GWAS_ID_7942 RMVar_hsa_circ_79074,RMVar_hsa_circ_177008 112959 RMVar_ID_112959 Human_SNP_ID_826314005 m1A Human chr16 + 494846 494846 494846 GATCACATGAGCCTGGGAGGTCGAGGCTGCAGAGGTGGGAGGATCACATGAGCCGGGGAGGTCGA GATCACATGAGCCTGGGAGGTCGAGGCTGCAGTGGTGGGAGGATCACATGAGCCGGGGAGGTCGA A T RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:494741..494900;chr16:494650..494975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_475474,Human_RBP_ID_816098,Human_RBP_ID_3503746,Human_RBP_ID_8183908,Human_RBP_ID_12756267,Human_RBP_ID_18418836,Human_RBP_ID_22715197,Human_RBP_ID_22940109 RMVar_hsa_circ_103523,RMVar_hsa_circ_175355,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_93194,RMVar_hsa_circ_175361,RMVar_hsa_circ_94016,RMVar_hsa_circ_175360,RMVar_hsa_circ_175357,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359,RMVar_hsa_circ_117968,RMVar_hsa_circ_272740,RMVar_hsa_circ_175362,RMVar_hsa_circ_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 112960 RMVar_ID_112960 Human_SNP_ID_826316881 m1A Human chr16 - 75629468 75629468 75629468 TTGTCATGAAGAAAGAGATATGCAATGCGTATACTGAGCTGAATGATCCCATGCGGCAGCGGCAG TTGTCATGAAGAAAGAGATATGCAATGCGTATGCTGAGCTGAATGATCCCATGCGGCAGCGGCAG T C KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75629372..75629489 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_1846862,Human_RBP_ID_8810470,Human_RBP_ID_9065661,Human_RBP_ID_22442220,Human_RBP_ID_23700740,Human_RBP_ID_27246165 Human_Splice_Rec_1741332,Human_Splice_Rec_1741333,Human_Splice_Rec_1741358,Human_Splice_Rec_1741359,Human_Splice_Rec_1741388,Human_Splice_Rec_1741389 Human_miRNA_ID_2565564 RMVar_hsa_circ_94319,RMVar_hsa_circ_103798,RMVar_hsa_circ_180085,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086 112961 RMVar_ID_112961 Human_SNP_ID_826329234 m1A Human chr16 - 87745263 87745263 87745263 GGCGGGTGCTGCAAGAGCAGAAGGCGGAGCAGAGGGCACCCTATGGCCGGCCCCAGGGCGGGTGT GGCGGGTGCTGCAAGAGCAGAAGGCGGAGCAGGGGGCACCCTATGGCCGGCCCCAGGGCGGGTGT T C KLHDC4,AC010536.2 Ensembl:ENSG00000104731,Ensembl:ENSG00000260671 Protein coding,lincRNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:87745213..87745444 26863196 MeRIP-seq:(Medium) rs8059456 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_261696,Human_RBP_ID_5647126,Human_RBP_ID_8184946,Human_RBP_ID_9420825,Human_RBP_ID_12839373 GWAS_ID_9518,GWAS_ID_9519,GWAS_ID_9520,GWAS_ID_9521,GWAS_ID_9522,GWAS_ID_9523,GWAS_ID_9524,GWAS_ID_9525,GWAS_ID_9526,GWAS_ID_9527,GWAS_ID_9528,GWAS_ID_9529,GWAS_ID_9530,GWAS_ID_9531 RMVar_hsa_circ_8657,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_51008,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_301519,RMVar_hsa_circ_274040,RMVar_hsa_circ_180437 112962 RMVar_ID_112962 Human_SNP_ID_826329273 m1A Human chr16 - 31466789 31466789 31466789 CTGCCTCTTCACCTGCTGCCTCCACAAGCCCCACCAGGGCCAGACCCCGCTTCCTCGGGCACTGC CTGCCTCTTCACCTGCTGCCTCCACAAGCCCCTCCAGGGCCAGACCCCGCTTCCTCGGGCACTGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:31466740..31466852 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 112963 RMVar_ID_112963 Human_SNP_ID_826329476 m1A Human chr16 - 46971426 46971426 46971426 GATGATATTTTCTCTCACATTTTTGGTGGGGGATTGTTCGGCTTCATGGGCAATCAGAGTAGAAG GATGATATTTTCTCTCACATTTTTGGTGGGGGGTTGTTCGGCTTCATGGGCAATCAGAGTAGAAG T C DNAJA2 Ensembl:ENSG00000069345 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:46971376..46971599 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_43710,Human_RBP_ID_4400619,Human_RBP_ID_6514569,Human_RBP_ID_8807971,Human_RBP_ID_9062356,Human_RBP_ID_9340941,Human_RBP_ID_9372779,Human_RBP_ID_12741111,Human_RBP_ID_17254382,Human_RBP_ID_17877199 Human_Splice_Rec_1708341,Human_Splice_Rec_1708357,Human_Splice_Rec_1708371 RMVar_hsa_circ_4706,RMVar_hsa_circ_37170,RMVar_hsa_circ_19704,RMVar_hsa_circ_57494 112964 RMVar_ID_112964 Human_SNP_ID_826329807 m1A Human chr16 + 88076829 88076829 88076829 GCGGGGAACAGCATCCTATCAACTGAAAGAGCAGCCGCCGCCGCCCCCAGCCGGAGACCCCTTTC GCGGGGAACAGCATCCTATCAACTGAAAGAGCCGCCGCCGCCGCCCCCAGCCGGAGACCCCTTTC A C BANP Ensembl:ENSG00000172530 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:88076789..88076877 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus 112965 RMVar_ID_112965 Human_SNP_ID_826330042 m1A Human chr16 + 58016694 58016694 58016694 TTTCAAGGAGGGAAGAGTCCACTGTGTGAGATACTGCTGGGTGCGTACGAGGCGGACAGCGAAGT TTTCAAGGAGGGAAGAGTCCACTGTGTGAGATGCTGCTGGGTGCGTACGAGGCGGACAGCGAAGT A G USB1 Ensembl:ENSG00000103005 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:58016646..58016940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_818676 RMVar_hsa_circ_83965,RMVar_hsa_circ_85931,RMVar_hsa_circ_178740,RMVar_hsa_circ_23230,RMVar_hsa_circ_8193,RMVar_hsa_circ_178743,RMVar_hsa_circ_376785,RMVar_hsa_circ_178744 112966 RMVar_ID_112966 Human_SNP_ID_826333501 m1A Human chr16 - 1783038 1783038 1783038 CTGGAGCGGCTCCGCACCCTGGCCCGCCACTCACCGGCCGCCGCCTCCATCCCGCCGCCTCCAGG CTGGAGCGGCTCCGCACCCTGGCCCGCCACTCCCCGGCCGCCGCCTCCATCCCGCCGCCTCCAGG T G SPSB3 Ensembl:ENSG00000162032 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr16:1783000..1783200;chr16:1782926..1783150 26863410,26863196 MeRIP-seq:(Medium) rs1334808667 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 112967 RMVar_ID_112967 Human_SNP_ID_826342178 m1A Human chr16 - 15033345 15033345 15033345 CGGGCTGTGGCCGCAATGGTCTCCACGAGCTCAGCAGCATCGACGTTGTCGCTCGCCATGCCGAC CGGGCTGTGGCCGCAATGGTCTCCACGAGCTCGGCAGCATCGACGTTGTCGCTCGCCATGCCGAC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:15033296..15033445 26863196 MeRIP-seq:(Medium) rs902659863 Functional Loss SNV ICGC 33..33 33 SARC 1 - 112968 RMVar_ID_112968 Human_SNP_ID_826343924 m1A Human chr16 + 30399069 30399069 30399069 TGACGCCCTTTGGGATAGGGGATGGTAGGGCAAGGCCCCTCAAGCAGGAGGCAGCAACAGGACTG TGACGCCCTTTGGGATAGGGGATGGTAGGGCAGGGCCCCTCAAGCAGGAGGCAGCAACAGGACTG A G ZNF48 Ensembl:ENSG00000180035 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:30399031..30399118 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_17875355 Human_miRNA_ID_2390853,Human_miRNA_ID_2592098 RMVar_hsa_circ_77856,RMVar_hsa_circ_177877 112969 RMVar_ID_112969 Human_SNP_ID_826345035 m1A Human chr16 + 30757049 30757049 30757049 CCTTTTCCCATCATGGGCCCTGAAGAGGAGGGAGACTCTGCTGCTATAACTGAGGATGAGGCCGT CCTTTTCCCATCATGGGCCCTGAAGAGGAGGGCGACTCTGCTGCTATAACTGAGGATGAGGCCGT A C PHKG2 Ensembl:ENSG00000156873 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:30756998..30757149 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus Human_RBP_ID_473031,Human_RBP_ID_12721142,Human_RBP_ID_18437573,Human_RBP_ID_22054070,Human_RBP_ID_23209622,Human_RBP_ID_27441866 Human_miRNA_ID_364328,Human_miRNA_ID_371546,Human_miRNA_ID_1239354,Human_miRNA_ID_1455127 112970 RMVar_ID_112970 Human_SNP_ID_826348126 m1A Human chr16 + 2519819 2519819 2519819 CCACCCCTCCTCATTCCAGAACGAACAGCCTGACACATACGCACGGGGCCGCCGCCCCCAGTAGT CCACCCCTCCTCATTCCAGAACGAACAGCCTGGCACATACGCACGGGGCCGCCGCCCCCAGTAGT A G AC093525.2,ATP6V0C,AC093525.1 Ensembl:ENSG00000260272,Ensembl:ENSG00000185883,Ensembl:ENSG00000259784 Protein coding,Protein coding,Protein coding 3'UTR,3'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2519586..2520144 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_45687,Human_RBP_ID_471324,Human_RBP_ID_1177513,Human_RBP_ID_1281504,Human_RBP_ID_1840421,Human_RBP_ID_5113323,Human_RBP_ID_5317346,Human_RBP_ID_8430684,Human_RBP_ID_12703982,Human_RBP_ID_17253608,Human_RBP_ID_17485811,Human_RBP_ID_17652886,Human_RBP_ID_17874270,Human_RBP_ID_18939910,Human_RBP_ID_21888714,Human_RBP_ID_23684568,Human_RBP_ID_26328500,Human_RBP_ID_26440260,Human_RBP_ID_26941178,Human_RBP_ID_27239374,Human_RBP_ID_27440558 RMVar_hsa_circ_110319,RMVar_hsa_circ_175779,RMVar_hsa_circ_78257,RMVar_hsa_circ_106510,RMVar_hsa_circ_175781,RMVar_hsa_circ_175782 112971 RMVar_ID_112971 Human_SNP_ID_826361699 m1A Human chr16 - 75641665 75641665 75641665 AGAAGAAAGTAGCAGAGAAGGAGGCCAAACAGAAAGAGCTCAGTGAGAAACAGCTAAGCCAAGCC AGAAGAAAGTAGCAGAGAAGGAGGCCAAACAGTAAGAGCTCAGTGAGAAACAGCTAAGCCAAGCC T A KARS1 Ensembl:ENSG00000065427 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:75641507..75641775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_43691,Human_RBP_ID_893646,Human_RBP_ID_1846886,Human_RBP_ID_4384798,Human_RBP_ID_9373256,Human_RBP_ID_12818627,Human_RBP_ID_18411409,Human_RBP_ID_22205766,Human_RBP_ID_26329251 Human_Splice_Rec_1741312,Human_Splice_Rec_1741338,Human_Splice_Rec_1741370,Human_Splice_Rec_1741396,Human_Splice_Rec_1741406,Human_Splice_Rec_1741418,Human_Splice_Rec_1741432,Human_Splice_Rec_1741444 RMVar_hsa_circ_94319,RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180086,RMVar_hsa_circ_44041,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277,RMVar_hsa_circ_180092,RMVar_hsa_circ_283420,RMVar_hsa_circ_367501,RMVar_hsa_circ_378999 112972 RMVar_ID_112972 Human_SNP_ID_826366393 m1A Human chr16 + 8895727 8895727 8895727 CTTCTTGATGAACACCAATGATTTTGTAGCTTACAATTTCTAGCAGCCTGAACAGAGAGGAAAAA CTTCTTGATGAACACCAATGATTTTGTAGCTTGCAATTTCTAGCAGCCTGAACAGAGAGGAAAAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:8895676..8895750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck 112973 RMVar_ID_112973 Human_SNP_ID_826379574 m1A Human chr16 - 58515882 58515882 58515882 CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCACCTTGGGACTCAGCTCCAGCCCCACCCGCCGG CGCGGGTCCTCCGCCCGCCGGCTCGCTCGCTCCCCTTGGGACTCAGCTCCAGCCCCACCCGCCGG T G lnc-CNOT1-3 RNACentral:URS00009B655F lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:58515765..58516073 26863196 MeRIP-seq:(Medium) rs1046247861 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4374946,Human_RBP_ID_12764584 112974 RMVar_ID_112974 Human_SNP_ID_826388665 m1A Human chr16 + 2831436 2831436 2831436 TCTGCTTGGAGTGACTAAGGCTCGGGAGGTCCAGGCTCGGCCAGAGGCAGCTCATATGTGGGCCA TCTGCTTGGAGTGACTAAGGCTCGGGAGGTCCCGGCTCGGCCAGAGGCAGCTCATATGTGGGCCA A C ZG16B Ensembl:ENSG00000162078 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:2831427..2831522 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 112975 RMVar_ID_112975 Human_SNP_ID_826391632 m1A Human chr16 + 727510 727510 727510 GGAGCAGGCACCGGTGGCCGAGCTCCGTGACCATGAAGGTCAAGGTCATCCCCGTGCTCGAGGAC GGAGCAGGCACCGGTGGCCGAGCTCCGTGACCGTGAAGGTCAAGGTCATCCCCGTGCTCGAGGAC A G HAGHL Ensembl:ENSG00000103253 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:727067..728104 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_234721,Human_RBP_ID_890179,Human_RBP_ID_3946928,Human_RBP_ID_17121324,Human_RBP_ID_18684863,Human_RBP_ID_22051775 Human_Splice_Rec_1656324,Human_Splice_Rec_1656334,Human_Splice_Rec_1656346,Human_Splice_Rec_1656348,Human_Splice_Rec_1656358 112976 RMVar_ID_112976 Human_SNP_ID_826403638 m1A Human chr16 - 30070252 30070252 30070252 AGGCGGCCTCCTCTTCAAGAGTGGGAGGGGGCAGGGCCTGGAGTGTTGGGGGCAGCCTGGGAACA AGGCGGCCTCCTCTTCAAGAGTGGGAGGGGGCGGGGCCTGGAGTGTTGGGGGCAGCCTGGGAACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30070207..30070340 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 15 uterus RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 112977 RMVar_ID_112977 Human_SNP_ID_826405030 m1A Human chr16 - 84618054 84618054 84618054 CCGTCCGCAGTGGAAGCCGCCGCCGCGCTCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGC CCGTCCGCAGTGGAAGCCGCCGCCGCGCTCGCCGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGC T G COTL1 Ensembl:ENSG00000103187 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84617778..84618077 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_233378,Human_RBP_ID_4394037,Human_RBP_ID_22532833 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 112978 RMVar_ID_112978 Human_SNP_ID_826408876 m1A Human chr16 + 11345710 11345710 11345710 CGGCGAGGCTCGGCTGAGGGACCCGAGCGGGGACTTCTCGGTCCGCGGCCTGGAGCGGGTGCCGC CGGCGAGGCTCGGCTGAGGGACCCGAGCGGGGGCTTCTCGGTCCGCGGCCTGGAGCGGGTGCCGC A G RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:11345561..11345709 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_234160,Human_RBP_ID_1002835,Human_RBP_ID_4395760,Human_RBP_ID_5142694,Human_RBP_ID_5495081,Human_RBP_ID_8804460,Human_RBP_ID_9353183,Human_RBP_ID_17871433,Human_RBP_ID_22442365,Human_RBP_ID_23677902 Human_Splice_Rec_1677819,Human_Splice_Rec_1677821 RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 112979 RMVar_ID_112979 Human_SNP_ID_826412284 m1A Human chr16 - 85799754 85799754 85799754 CTGGCGGCGCCGCACCGGCCACCTCCTGTCTCACCTGCCGCCACTGCCCGCCGCGACCGCCCTCT CTGGCGGCGCCGCACCGGCCACCTCCTGTCTCCCCTGCCGCCACTGCCCGCCGCGACCGCCCTCT T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:85799626..85799863;chr16:85799651..85799854;chr16:85799651..85799828 26863196 MeRIP-seq:(Medium) rs1029165692 Functional Loss SNV ICGC 33..33 33 BOCA 1 - 112980 RMVar_ID_112980 Human_SNP_ID_826420333 m1A Human chr16 + 696987 696987 696987 GCAGCACGTTGTAGAGCTCCTTGGCATGCAGCACCGGCGTGAGGCCTGCCCAGAACTTGGGCTGG GCAGCACGTTGTAGAGCTCCTTGGCATGCAGCGCCGGCGTGAGGCCTGCCCAGAACTTGGGCTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:696938..697089 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 112981 RMVar_ID_112981 Human_SNP_ID_826422215 m1A Human chr16 + 70427238 70427236 70427238 CACTAATTTCTGGATGCTATCCTTTAGACAGTATACCTTAGTAGAGGTATCCAAAAAGTATCTCA CACTAATTTCTGGATGCTATCCTTTAGACAG__TACCTTAGTAGAGGTATCCAAAAAGTATCTCA GTA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:70427235..70427318 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 PAAD 1 - 112982 RMVar_ID_112982 Human_SNP_ID_826424165 m1A Human chr16 + 2047780 2047780 2047780 CCCTACACCCCCGCGGCCCAGCCCCGGGTCCCAGGCTCCGGCTCCGGGTCAGCATCCTCGCGCTC CCCTACACCCCCGCGGCCCAGCCCCGGGTCCCGGGCTCCGGCTCCGGGTCAGCATCCTCGCGCTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2047613..2047850 26863196 MeRIP-seq:(Medium) rs781328762 Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 2 uterus 112983 RMVar_ID_112983 Human_SNP_ID_826435076 m1A Human chr16 - 89283009 89283009 89283009 TTCTGACAAGCAGCACCCTGAGAGGCAGAAGGACAAGGAGCCCAGAGACAGGAGAAAGGACCGAG TTCTGACAAGCAGCACCCTGAGAGGCAGAAGGGCAAGGAGCCCAGAGACAGGAGAAAGGACCGAG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89282743..89283378 26863196 MeRIP-seq:(Medium) rs1447641697 Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_5524758,Human_RBP_ID_24544439 Human_miRNA_ID_2425195,Human_miRNA_ID_2434857 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 112984 RMVar_ID_112984 Human_SNP_ID_826441524 m1A Human chr16 - 3284207 3284207 3284207 AACCACAGATAAAACAGCTCTCTCTCTCTCTCACCTGTTGTCTCAGTCTCCCAAGCTCTCTCTGC AACCACAGATAAAACAGCTCTCTCTCTCTCTCTCCTGTTGTCTCAGTCTCCCAAGCTCTCTCTGC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3284157..3285161 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 4 head and neck 112985 RMVar_ID_112985 Human_SNP_ID_826447613 m1A Human chr16 + 23689623 23689622 23689623 TGCCCTACCTACGGACCTGGTTCCGCACCCGCAGCGCCATCATCCTGCACCTCAGCAACGGCAGC TGCCCTACCTACGGACCTGGTTCCGCACCCGC_GCGCCATCATCCTGCACCTCAGCAACGGCAGC CA C PLK1 Ensembl:ENSG00000166851 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:23689476..23689636 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_6502107,Human_RBP_ID_8430164,Human_RBP_ID_8805847,Human_RBP_ID_12696932,Human_RBP_ID_17253521,Human_RBP_ID_17653320,Human_RBP_ID_22441855,Human_RBP_ID_26940738,Human_RBP_ID_27440309 Human_Splice_Rec_1692555,Human_Splice_Rec_1692577 Human_miRNA_ID_2975769 RMVar_hsa_circ_6687,RMVar_hsa_circ_94720,RMVar_hsa_circ_100779,RMVar_hsa_circ_117169,RMVar_hsa_circ_177353,RMVar_hsa_circ_177354,RMVar_hsa_circ_177355,RMVar_hsa_circ_99883,RMVar_hsa_circ_96131,RMVar_hsa_circ_177356,RMVar_hsa_circ_177357 112986 RMVar_ID_112986 Human_SNP_ID_826451422 m1A Human chr16 + 2762625 2762625 2762625 AGAGGGAGGTCTCGGTCTAGGACACCAAGACGAGGAAGATCCCGCAGTAGAAGCTTAGTTAGACG AGAGGGAGGTCTCGGTCTAGGACACCAAGACGGGGAAGATCCCGCAGTAGAAGCTTAGTTAGACG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2762576..2762650 26863196 MeRIP-seq:(Medium) rs1453712613 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_818613,Human_RBP_ID_1515510,Human_RBP_ID_1840690,Human_RBP_ID_3493642,Human_RBP_ID_5571617,Human_RBP_ID_6505300,Human_RBP_ID_8431026,Human_RBP_ID_9823953,Human_RBP_ID_12708834,Human_RBP_ID_17689971,Human_RBP_ID_18529704,Human_RBP_ID_18676440,Human_RBP_ID_20093630,Human_RBP_ID_26329692 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 112987 RMVar_ID_112987 Human_SNP_ID_826453202 m1A Human chr16 + 84001937 84001937 84001937 TCTTGGTGCCAGGTAGGGGGCAAAGGCCTGGAACTGCAGTGGCCACCTGACTGGAGAGAAGGGCA TCTTGGTGCCAGGTAGGGGGCAAAGGCCTGGACCTGCAGTGGCCACCTGACTGGAGAGAAGGGCA A C NECAB2 Ensembl:ENSG00000103154 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:84001922..84002022 32194978 MeRIP-seq:(Medium) rs2271301 Functional Loss SNV ICGC 33..33 33 COCA 2 - GWAS_ID_9504,GWAS_ID_9505 112988 RMVar_ID_112988 Human_SNP_ID_826459840 m1A Human chr16 - 29995219 29995218 29995220 TGGTGCATAGTTTGCCCTCTTGGCGCACACACAGGTGGATGAAGCCGCTTCCAGGGAAGACAAAC TGGTGCATAGTTTGCCCTCTTGGCGCACACA__GGTGGATGAAGCCGCTTCCAGGGAAGACAAAC CTG C HIRIP3 Ensembl:ENSG00000149929 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:29995181..29995392 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 CESC 1 - Human_RBP_ID_894011,Human_RBP_ID_4362448,Human_RBP_ID_23256679 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 112989 RMVar_ID_112989 Human_SNP_ID_826467650 m1A Human chr16 - 23510447 23510447 23510447 GAGCGCCAGGACGCTACAGCGGCTGAAGAGGCAGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGA GAGCGCCAGGACGCTACAGCGGCTGAAGAGGCGGTGGCGCCCGCGGCCGCAGCGTCGGGGCTGGA T C GGA2 Ensembl:ENSG00000103365 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr16:23510323..23510478;chr16:23510326..23510475 26863196 MeRIP-seq:(Medium) rs978183015 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_234750,Human_RBP_ID_4392912,Human_RBP_ID_9374038,Human_RBP_ID_18418961 112990 RMVar_ID_112990 Human_SNP_ID_826473549 m1A Human chr16 - 28845963 28845963 28845963 TGCGCGACAAGCCACATGTGAATGTGGGTACCATCGGCCATGTGGACCACGGGAAGACCACGCTG TGCGCGACAAGCCACATGTGAATGTGGGTACCGTCGGCCATGTGGACCACGGGAAGACCACGCTG T C TUFM Ensembl:ENSG00000178952 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:28845901..28845975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_471863,Human_RBP_ID_1516026,Human_RBP_ID_1841015,Human_RBP_ID_2472695,Human_RBP_ID_4360962,Human_RBP_ID_9372589,Human_RBP_ID_17874800,Human_RBP_ID_22441388,Human_RBP_ID_26810172 Human_Splice_Rec_1698091,Human_Splice_Rec_1698113 112991 RMVar_ID_112991 Human_SNP_ID_826476208 m1A Human chr16 + 635667 635667 635667 CATGGGCCATGTTGATGCAGAGCAACAGGTCCAGCGACTGTGGCAGGATCCCGCCCCAGTGCTCC CATGGGCCATGTTGATGCAGAGCAACAGGTCCGGCGACTGTGGCAGGATCCCGCCCCAGTGCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:635664..635788 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 8 caecum,large intestine 112992 RMVar_ID_112992 Human_SNP_ID_826483218 m1A Human chr16 + 4698807 4698807 4698807 CCCCATCCCCCACCCAGCCACTCACCTTGTGCAGCTGGATGGCGAGCTCCTGCATCTCAGCCTCC CCCCATCCCCCACCCAGCCACTCACCTTGTGCGGCTGGATGGCGAGCTCCTGCATCTCAGCCTCC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:4698393..4698943 32194978 MeRIP-seq:(Medium) rs1279293085 Functional Loss SNV ICGC 33..33 33 STAD 1 - 112993 RMVar_ID_112993 Human_SNP_ID_826495346 m1A Human chr16 - 29879944 29879944 29879944 AACCTTCTCGTGCCTCCCAGGATATGCCCTGGAGCCCCCTGGGCCCCCCAATGCCATCGAATGTG AACCTTCTCGTGCCTCCCAGGATATGCCCTGGTGCCCCCTGGGCCCCCCAATGCCATCGAATGTG T A SEZ6L2 Ensembl:ENSG00000174938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29878419..29879957 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_22760219 Human_Splice_Rec_1700419,Human_Splice_Rec_1700453,Human_Splice_Rec_1700487,Human_Splice_Rec_1700519,Human_Splice_Rec_1700551,Human_Splice_Rec_1700581 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_4491,RMVar_hsa_circ_325994,RMVar_hsa_circ_332823,RMVar_hsa_circ_177790 112994 RMVar_ID_112994 Human_SNP_ID_826495517 m1A Human chr16 - 29861227 29861216 29861227 GAACCCGGTTTGGGGCCATGCTGGACATGCTGACGGACCGCTGCTCCACCATGTGCCTGTTGGTC GAACCCGGTTTGGGGCCATGCTGGACATGCTG___________CTCCACCATGTGCCTGTTGGTC GCAGCGGTCCGT G CDIPT Ensembl:ENSG00000103502 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:29861176..29861306 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..43 33 OV 1 - Human_RBP_ID_472235,Human_RBP_ID_4394554,Human_RBP_ID_5142761 Human_Splice_Rec_1700304,Human_Splice_Rec_1700320,Human_Splice_Rec_1700332,Human_Splice_Rec_1700342,Human_Splice_Rec_1700354,Human_Splice_Rec_1700364,Human_Splice_Rec_1700372,Human_Splice_Rec_1700380 Human_miRNA_ID_1454921,Human_miRNA_ID_2756883,Human_miRNA_ID_2756884,Human_miRNA_ID_2756885,Human_miRNA_ID_2756886 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_96910,RMVar_hsa_circ_86629,RMVar_hsa_circ_177780,RMVar_hsa_circ_177781,RMVar_hsa_circ_177786,RMVar_hsa_circ_283262,RMVar_hsa_circ_378686 112995 RMVar_ID_112995 Human_SNP_ID_826498781 m1A Human chr16 + 56559 56559 56559 CCCCTCTTGCAGGTCCTACGTGTGGAGGACGTACCATCTGACCTCTGCAGGAGAGAAACTCACGG CCCCTCTTGCAGGTCCTACGTGTGGAGGACGTGCCATCTGACCTCTGCAGGAGAGAAACTCACGG A G SNRNP25 Ensembl:ENSG00000161981 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:56555..57126 32194978 MeRIP-seq:(Medium) rs779593421 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_1837861,Human_RBP_ID_4349699,Human_RBP_ID_9371980,Human_RBP_ID_17883617,Human_RBP_ID_22651237,Human_RBP_ID_23114005 Human_Splice_Rec_1652246,Human_Splice_Rec_1652247,Human_Splice_Rec_1652254,Human_Splice_Rec_1652255,Human_Splice_Rec_1652264,Human_Splice_Rec_1652265,Human_Splice_Rec_1652276,Human_Splice_Rec_1652280,Human_Splice_Rec_1652281,Human_Splice_Rec_1652285 112996 RMVar_ID_112996 Human_SNP_ID_826505878 m1A Human chr16 + 1505461 1505461 1505461 AGGAGCTGTCTAGGCCTGGGTGCCTCGGGAGGACTCCCCAACCTGGCTCCCCAAGTCCCAACACC AGGAGCTGTCTAGGCCTGGGTGCCTCGGGAGGTCTCCCCAACCTGGCTCCCCAAGTCCCAACACC A T TELO2 Ensembl:ENSG00000100726 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1505391..1506614 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_888249,Human_RBP_ID_3946993,Human_RBP_ID_18673551 Human_Splice_Rec_1659532,Human_Splice_Rec_1659552,Human_Splice_Rec_1659564,Human_Splice_Rec_1659568 RMVar_hsa_circ_11811,RMVar_hsa_circ_116150,RMVar_hsa_circ_335860,RMVar_hsa_circ_25500,RMVar_hsa_circ_94017,RMVar_hsa_circ_175498,RMVar_hsa_circ_118219,RMVar_hsa_circ_175499,RMVar_hsa_circ_111412,RMVar_hsa_circ_175500,RMVar_hsa_circ_88212,RMVar_hsa_circ_175501,RMVar_hsa_circ_175502,RMVar_hsa_circ_30704,RMVar_hsa_circ_175503,RMVar_hsa_circ_90260,RMVar_hsa_circ_118482,RMVar_hsa_circ_175504,RMVar_hsa_circ_175506,RMVar_hsa_circ_106055,RMVar_hsa_circ_376714,RMVar_hsa_circ_175505,RMVar_hsa_circ_325091 112997 RMVar_ID_112997 Human_SNP_ID_826522336 m1A Human chr16 - 11846533 11846533 11846533 TCAAGAGAGATCAATGACTGTATAGGTGGAACAGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG TCAAGAGAGATCAATGACTGTATAGGTGGAACGGTCTTAAACATTTCTAAAAGTGGTTCTTGCAG T C RSL1D1 Ensembl:ENSG00000171490 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8052900 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,liver hepatocellular_carcinoma 6 liver,stomach,haematopoietic and lymphoid tissue Human_RBP_ID_45517,Human_RBP_ID_1364916,Human_RBP_ID_1838001,Human_RBP_ID_3491207,Human_RBP_ID_5184227,Human_RBP_ID_5571422,Human_RBP_ID_6493044,Human_RBP_ID_12665627,Human_RBP_ID_17188445,Human_RBP_ID_17252890,Human_RBP_ID_17689600,Human_RBP_ID_17871530,Human_RBP_ID_18672980,Human_RBP_ID_22442366,Human_RBP_ID_26446569,Human_RBP_ID_27236667,Human_RBP_ID_27656268 Human_Splice_Rec_1678536,Human_Splice_Rec_1678537,Human_Splice_Rec_1678550,Human_Splice_Rec_1678551,Human_Splice_Rec_1678574,Human_Splice_Rec_1678575,Human_Splice_Rec_1678603,Human_Splice_Rec_1678614,Human_Splice_Rec_1678615,Human_Splice_Rec_1678628,Human_Splice_Rec_1678636 Human_miRNA_ID_2744050,Human_miRNA_ID_2744051 RMVar_hsa_circ_83192,RMVar_hsa_circ_4236,RMVar_hsa_circ_126224,RMVar_hsa_circ_280181,RMVar_hsa_circ_51417,RMVar_hsa_circ_176322,RMVar_hsa_circ_264984,RMVar_hsa_circ_176323,RMVar_hsa_circ_273603,RMVar_hsa_circ_285418,RMVar_hsa_circ_326366,RMVar_hsa_circ_274815,RMVar_hsa_circ_119873,RMVar_hsa_circ_176325,RMVar_hsa_circ_176327,RMVar_hsa_circ_176328,RMVar_hsa_circ_176329,RMVar_hsa_circ_176326 112998 RMVar_ID_112998 Human_SNP_ID_826531956 m1A Human chr16 + 28834566 28834566 28834566 ACACCAGCCAGCCTCAGCCCCGCCGATGATGCAGGCCGCCGCGGCTGCTGGCCCGCCTCTGGTGG ACACCAGCCAGCCTCAGCCCCGCCGATGATGCTGGCCGCCGCGGCTGCTGGCCCGCCTCTGGTGG A T ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:28834425..28834706 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 7 lung Human_RBP_ID_234100,Human_RBP_ID_895943,Human_RBP_ID_17371362,Human_RBP_ID_22532780 Human_Splice_Rec_1697628,Human_Splice_Rec_1697668,Human_Splice_Rec_1697712,Human_Splice_Rec_1697756,Human_Splice_Rec_1697802,Human_Splice_Rec_1697844,Human_Splice_Rec_1697888,Human_Splice_Rec_1697932,Human_Splice_Rec_1698002,Human_Splice_Rec_1698028,Human_Splice_Rec_1698034,Human_Splice_Rec_1698042,Human_Splice_Rec_1698054,Human_Splice_Rec_1698066 Human_miRNA_ID_1239336,Human_miRNA_ID_1336403,Human_miRNA_ID_1455106 RMVar_hsa_circ_104153,RMVar_hsa_circ_177672,RMVar_hsa_circ_45278 112999 RMVar_ID_112999 Human_SNP_ID_826535983 m1A Human chr16 + 89740857 89740857 89740857 CAGCAGGCCCATCAAGGAGAAGAAGAAAAGGAAAACCAATAGCTGTAAATAAAAACGTGCACTTA CAGCAGGCCCATCAAGGAGAAGAAGAAAAGGACAACCAATAGCTGTAAATAAAAACGTGCACTTA A C ZNF276 Ensembl:ENSG00000158805 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:89740752..89740903 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_1526140,Human_RBP_ID_1848052,Human_RBP_ID_21889017 113000 RMVar_ID_113000 Human_SNP_ID_826552484 m1A Human chr16 - 297228 297228 297228 AGGCCAGGGCGACTCGCAGCTCTTGCCCTTGCAGTGGGAAGGTGGGCGTGGCGTGCAAAAGAAAT AGGCCAGGGCGACTCGCAGCTCTTGCCCTTGCTGTGGGAAGGTGGGCGTGGCGTGCAAAAGAAAT T A AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:297201..297250 26863196 MeRIP-seq:(Medium) rs1364610136 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM,LICA 2 - Human_RBP_ID_22542048 RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_117231,RMVar_hsa_circ_29731,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_48295,RMVar_hsa_circ_265783,RMVar_hsa_circ_286556,RMVar_hsa_circ_175319,RMVar_hsa_circ_175320 113001 RMVar_ID_113001 Human_SNP_ID_826557153 m1A Human chr16 + 11020137 11020137 11020137 GCATATTTATTCTCCAACATGAGCATGTGTATAAATCTAGGGCTGAAAAGCTGTCTGGACTCATC GCATATTTATTCTCCAACATGAGCATGTGTATTAATCTAGGGCTGAAAAGCTGTCTGGACTCATC A T CLEC16A Ensembl:ENSG00000038532 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:11020131..11020215 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 face Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 2 skin,head and neck Human_RBP_ID_3491043,Human_RBP_ID_22542227,Human_RBP_ID_22651687 RMVar_hsa_circ_14509,RMVar_hsa_circ_96819,RMVar_hsa_circ_348620,RMVar_hsa_circ_11922,RMVar_hsa_circ_99138,RMVar_hsa_circ_57611,RMVar_hsa_circ_176229,RMVar_hsa_circ_269480,RMVar_hsa_circ_45788,RMVar_hsa_circ_33678,RMVar_hsa_circ_120200,RMVar_hsa_circ_119442,RMVar_hsa_circ_176231,RMVar_hsa_circ_118053,RMVar_hsa_circ_176233,RMVar_hsa_circ_76996,RMVar_hsa_circ_82949,RMVar_hsa_circ_176235,RMVar_hsa_circ_176237,RMVar_hsa_circ_176236,RMVar_hsa_circ_176234,RMVar_hsa_circ_293894,RMVar_hsa_circ_94607,RMVar_hsa_circ_176241,RMVar_hsa_circ_176242 113002 RMVar_ID_113002 Human_SNP_ID_826561407 m1A Human chr16 - 1771305 1771305 1771305 GATTGTGCGGCGCTTCGAGAGGAAGGGCTTCAAGTTGGTGGCGCTGAAGCTGGTGCAGGTGGGGG GATTGTGCGGCGCTTCGAGAGGAAGGGCTTCAGGTTGGTGGCGCTGAAGCTGGTGCAGGTGGGGG T C NME3 Ensembl:ENSG00000103024 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:1770876..1771575;chr16:1770901..1771550 26863196 MeRIP-seq:(Medium) rs202165010 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder Human_RBP_ID_46074,Human_RBP_ID_1513138,Human_RBP_ID_4352730,Human_RBP_ID_23680933 Human_Splice_Rec_1660419,Human_Splice_Rec_1660427,Human_Splice_Rec_1660441,Human_Splice_Rec_1660447,Human_Splice_Rec_1660467 113003 RMVar_ID_113003 Human_SNP_ID_826563626 m1A Human chr16 + 69742161 69742161 69742161 AGCCAGGCGCTCCGGTGCTCACAGGCCATGGGACAGTCCAGTTCCCTGCAGACCCAGCGGGGCAT AGCCAGGCGCTCCGGTGCTCACAGGCCATGGGGCAGTCCAGTTCCCTGCAGACCCAGCGGGGCAT A G AC092115.4 Ensembl:ENSG00000262136 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:69727160..69744926 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_Splice_Rec_1733470 113004 RMVar_ID_113004 Human_SNP_ID_826565303 m1A Human chr16 + 28866788 28866788 28866788 GGGAAAGATGGACTCACCGTTTTGAGAGGCTGAGACTCAGTCGGGGAGGGGGCGCCTTGAAGGAT GGGAAAGATGGACTCACCGTTTTGAGAGGCTGGGACTCAGTCGGGGAGGGGGCGCCTTGAAGGAT A G SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:28866737..28867212 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_890484,Human_RBP_ID_3949048,Human_RBP_ID_5357871,Human_RBP_ID_5524288,Human_RBP_ID_8431561,Human_RBP_ID_9325032,Human_RBP_ID_12712667 Human_miRNA_ID_2947801 RMVar_hsa_circ_372710,RMVar_hsa_circ_177679 113005 RMVar_ID_113005 Human_SNP_ID_826569801 m1A Human chr16 + 75464567 75464567 75464567 CAGGCTCAGGATCTGCTGCAGGAGCCCGGCCGACCCGCCGCTGCCGCCGCTCCCCTCGCGCTCCA CAGGCTCAGGATCTGCTGCAGGAGCCCGGCCGCCCCGCCGCTGCCGCCGCTCCCCTCGCGCTCCA A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:75464516..75464690 26863196 MeRIP-seq:(Medium) rs752230193 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mast_cell_neoplasm 6 haematopoietic and lymphoid tissue 113006 RMVar_ID_113006 Human_SNP_ID_826576920 m1A Human chr16 + 3675374 3675374 3675374 CCTTCCATTCAAGTACAAGGGGAAGCTGACGAAGTTGCTGTACTTCGTTACCACATCTGGAAGGG CCTTCCATTCAAGTACAAGGGGAAGCTGACGAGGTTGCTGTACTTCGTTACCACATCTGGAAGGG A G DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:3674904..3676111 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach 113007 RMVar_ID_113007 Human_SNP_ID_826587145 m1A Human chr16 + 29810185 29810185 29810185 TCCCACAGCTGTGGGCTCCCTCTCGGGGGCGGAGGGGGTGCCTGTGAGCTCTCAGCCACTTCCCT TCCCACAGCTGTGGGCTCCCTCTCGGGGGCGGGGGGGGTGCCTGTGAGCTCTCAGCCACTTCCCT A G MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA CDS,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:29810176..29810200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 9 head and neck Human_RBP_ID_277404,Human_RBP_ID_472119,Human_RBP_ID_1003894,Human_RBP_ID_1177704,Human_RBP_ID_1516257,Human_RBP_ID_1841127,Human_RBP_ID_5142760,Human_RBP_ID_5183918,Human_RBP_ID_5237248,Human_RBP_ID_5259665,Human_RBP_ID_5576570,Human_RBP_ID_6506857,Human_RBP_ID_8088364,Human_RBP_ID_8431776,Human_RBP_ID_8806748,Human_RBP_ID_9325052,Human_RBP_ID_12714912,Human_RBP_ID_17486026,Human_RBP_ID_17874973,Human_RBP_ID_18677209,Human_RBP_ID_20112355,Human_RBP_ID_22532688,Human_RBP_ID_22800855,Human_RBP_ID_23686016 Human_Splice_Rec_1699984,Human_Splice_Rec_1699988,Human_Splice_Rec_1700019,Human_Splice_Rec_1700044,Human_Splice_Rec_1700063 Human_miRNA_ID_3188665,Human_miRNA_ID_3195622 RMVar_hsa_circ_26374 113008 RMVar_ID_113008 Human_SNP_ID_826588928 m1A Human chr16 - 3581338 3581338 3581338 CATGTTCACTAGCGGATTCCATTCTTTGGGTTAAAGCTGCCTCCAGCCTCAGGAGCAGTGTGGAG CATGTTCACTAGCGGATTCCATTCTTTGGGTTGAAGCTGCCTCCAGCCTCAGGAGCAGTGTGGAG T C SLX4 Ensembl:ENSG00000188827 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs75773027 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Clinvar_Rec_319,Clinvar_Rec_320,Clinvar_Rec_321,Clinvar_Rec_322,Clinvar_Rec_323,Clinvar_Rec_324,Clinvar_Rec_2691,Clinvar_Rec_2692,Clinvar_Rec_2693,Clinvar_Rec_2694,Clinvar_Rec_2695,Clinvar_Rec_2696 GWAS_ID_8882,GWAS_ID_8883,GWAS_ID_8884 113009 RMVar_ID_113009 Human_SNP_ID_826589533 m1A Human chr16 - 18788053 18788047 18788054 ACCTCACAGGCAGGCTAAACAAGGTAAGAACGAGTGATCTACACATTTCAAAGCTTTAAGAATTT ACCTCACAGGCAGGCTAAACAAGGTAAGAAC_______CTACACATTTCAAAGCTTTAAGAATTT GATCACTC G RPS15A Ensembl:ENSG00000134419 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:18788051..18788150 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..38 33 RECA 1 - Human_RBP_ID_233664,Human_RBP_ID_17607744,Human_RBP_ID_19073561 Human_Splice_Rec_1685040,Human_Splice_Rec_1685048,Human_Splice_Rec_1685058,Human_Splice_Rec_1685070,Human_Splice_Rec_1685078,Human_Splice_Rec_1685094,Human_Splice_Rec_1685104,Human_Splice_Rec_1685114,Human_Splice_Rec_1685130 RMVar_hsa_circ_122283,RMVar_hsa_circ_176773,RMVar_hsa_circ_77194,RMVar_hsa_circ_176774,RMVar_hsa_circ_176777,RMVar_hsa_circ_375183 113010 RMVar_ID_113010 Human_SNP_ID_826589985 m1A Human chr16 + 70483869 70483869 70483869 TGAACCTGGGGCTTACCTGCAAGAGGTCTCGGAATTTGTTGGACACGGCGGCCAAGTCAGAAAGG TGAACCTGGGGCTTACCTGCAAGAGGTCTCGGGATTTGTTGGACACGGCGGCCAAGTCAGAAAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:70482733..70483915 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine RMVar_hsa_circ_179634 113011 RMVar_ID_113011 Human_SNP_ID_826595321 m1A Human chr16 - 89293442 89293442 89293442 GCCACAACTCTGCCCCAGCTCCTCCCTCCGCAACCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA GCCACAACTCTGCCCCAGCTCCTCCCTCCGCAGCCCCAACTCTGCCCCAGCTCCTCCCTCCGCAA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:89293438..89293679;chr16:89293439..89293760 26863196 MeRIP-seq:(Medium) rs879457112 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 20 prostate Human_RBP_ID_3505851,Human_RBP_ID_17077738 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_95669,RMVar_hsa_circ_180608,RMVar_hsa_circ_325574 113012 RMVar_ID_113012 Human_SNP_ID_826596398 m1A Human chr16 - 2206123 2206123 2206123 CGGTGTGGTCGTAGCCTGCAGTGGCCAGGATGACCGGGTCACTGCCCACCGTGCCTGGGGAGGTG CGGTGTGGTCGTAGCCTGCAGTGGCCAGGATGGCCGGGTCACTGCCCACCGTGCCTGGGGAGGTG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2206026..2206209 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 8 liver 113013 RMVar_ID_113013 Human_SNP_ID_826600477 m1A Human chr16 - 57758345 57758345 57758345 TATGGCTGGCAGAGGCAGCCAGCGGGTGGGGGATTCTGCTGCTCGCTCACCTGCCTGGCTCGCTG TATGGCTGGCAGAGGCAGCCAGCGGGTGGGGGGTTCTGCTGCTCGCTCACCTGCCTGGCTCGCTG T C KIFC3 Ensembl:ENSG00000140859 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr16:57758266..57758417;chr16:57758251..57759466 32194978 MeRIP-seq:(Medium) rs1555589832 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_762605,Human_RBP_ID_3947699,Human_RBP_ID_5237544,Human_RBP_ID_23209365,Human_RBP_ID_26445179,Human_RBP_ID_26757356 113014 RMVar_ID_113014 Human_SNP_ID_826601584 m1A Human chr16 + 84700040 84700040 84700040 ATGTGCGGGCGAGAAGATGGCGGCGGCGGGGGAAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTC ATGTGCGGGCGAGAAGATGGCGGCGGCGGGGGGAGCAGCGTGAGCAGCCGGAGGATCGCGGAGTC A G USP10 Ensembl:ENSG00000103194 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:84699976..84700176 26863196 MeRIP-seq:(Medium) rs1049318683 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_763511,Human_RBP_ID_4386800,Human_RBP_ID_5316719,Human_RBP_ID_8812502,Human_RBP_ID_9285950,Human_RBP_ID_9326109,Human_RBP_ID_12829297,Human_RBP_ID_22053490,Human_RBP_ID_22441138,Human_RBP_ID_23114116,Human_RBP_ID_26329273,Human_RBP_ID_27446217 Human_Splice_Rec_1746449,Human_Splice_Rec_1746475,Human_Splice_Rec_1746483,Human_Splice_Rec_1746489,Human_Splice_Rec_1746495,Human_Splice_Rec_1746507,Human_Splice_Rec_1746527,Human_Splice_Rec_1746529,Human_Splice_Rec_1746537,Human_Splice_Rec_1746559,Human_Splice_Rec_1746587,Human_Splice_Rec_1746595,Human_Splice_Rec_1746613 113015 RMVar_ID_113015 Human_SNP_ID_826611894 m1A Human chr16 - 1185961 1185957 1185961 CCCCGTACACACCCCGCCTCCGGCCCCTACGCACGCCGTCTACTCACCCGCCCCGTACACACCCC CCCCGTACACACCCCGCCTCCGGCCCCTACGC____CGTCTACTCACCCGCCCCGTACACACCCC GGCGT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:1185930..1186079 26863196 MeRIP-seq:(Medium) rs1287639545 Functional Loss DEL ICGC 33..36 33 COCA 1 - 113016 RMVar_ID_113016 Human_SNP_ID_826619193 m1A Human chr16 - 88716481 88716481 88716481 CAGTGGGTCACGCTGTGTTCCCACCCCCAGGGACCTGGCGAAGGGAGGCACTGTGGAGTATGCCA CAGTGGGTCACGCTGTGTTCCCACCCCCAGGGGCCTGGCGAAGGGAGGCACTGTGGAGTATGCCA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88716399..88716724 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_44384,Human_RBP_ID_894386,Human_RBP_ID_3948060,Human_RBP_ID_4389163,Human_RBP_ID_5114022,Human_RBP_ID_8231935,Human_RBP_ID_9373340,Human_RBP_ID_18163093,Human_RBP_ID_18984421,Human_RBP_ID_26328252,Human_RBP_ID_26951724,Human_RBP_ID_27248070,Human_RBP_ID_27447070,Human_RBP_ID_27811317 Human_Splice_Rec_1749796,Human_Splice_Rec_1749814,Human_Splice_Rec_1749832,Human_Splice_Rec_1749848,Human_Splice_Rec_1749856 RMVar_hsa_circ_80974,RMVar_hsa_circ_88466,RMVar_hsa_circ_91942,RMVar_hsa_circ_126808,RMVar_hsa_circ_180531,RMVar_hsa_circ_90544,RMVar_hsa_circ_180532,RMVar_hsa_circ_180533,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180535,RMVar_hsa_circ_180536 113017 RMVar_ID_113017 Human_SNP_ID_826626556 m1A Human chr16 - 28104596 28104596 28104596 AGTCCACCGTGCTGGCCAGTGTCCAGAGGGGGATCGCTGAGGAGCAGATGGAGAATGAGCCCCAG AGTCCACCGTGCTGGCCAGTGTCCAGAGGGGGTTCGCTGAGGAGCAGATGGAGAATGAGCCCCAG T A XPO6 Ensembl:ENSG00000169180 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28104526..28104625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_6505248,Human_RBP_ID_12708661,Human_RBP_ID_18983499,Human_RBP_ID_22802936,Human_RBP_ID_22937580,Human_RBP_ID_23209311,Human_RBP_ID_26941600 Human_Splice_Rec_1695059,Human_Splice_Rec_1695109 RMVar_hsa_circ_42265,RMVar_hsa_circ_81172,RMVar_hsa_circ_177561,RMVar_hsa_circ_103755,RMVar_hsa_circ_302811,RMVar_hsa_circ_334227,RMVar_hsa_circ_345809,RMVar_hsa_circ_323953,RMVar_hsa_circ_279471,RMVar_hsa_circ_108269,RMVar_hsa_circ_101667,RMVar_hsa_circ_177562,RMVar_hsa_circ_177566,RMVar_hsa_circ_177568,RMVar_hsa_circ_177567,RMVar_hsa_circ_177564,RMVar_hsa_circ_177565,RMVar_hsa_circ_177563,RMVar_hsa_circ_177571,RMVar_hsa_circ_77939,RMVar_hsa_circ_99501,RMVar_hsa_circ_39330,RMVar_hsa_circ_177572,RMVar_hsa_circ_318251,RMVar_hsa_circ_336388,RMVar_hsa_circ_373692,RMVar_hsa_circ_102958,RMVar_hsa_circ_177574,RMVar_hsa_circ_29965,RMVar_hsa_circ_33566,RMVar_hsa_circ_10119,RMVar_hsa_circ_177575,RMVar_hsa_circ_177573 113018 RMVar_ID_113018 Human_SNP_ID_826627511 m1A Human chr16 - 84779080 84779080 84779080 CACTGGGCGCACACACAGCGCACACAGGGTTTACAGCAGGTCCACTCGGCGGTAATACAGGAGGT CACTGGGCGCACACACAGCGCACACAGGGTTTGCAGCAGGTCCACTCGGCGGTAATACAGGAGGT T C lnc-COTL1-2 RNACentral:URS00008B38D8 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84768201..84779474 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 113019 RMVar_ID_113019 Human_SNP_ID_826638799 m1A Human chr16 + 29810108 29810108 29810108 GGTACTGGTGAGGTTTGTCCAATGGCGGCGGCAGCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC GGTACTGGTGAGGTTTGTCCAATGGCGGCGGCGGCGGCAGCGGCGGCAGCGGCAGCAGCGGCAGC A G MAZ,AC009133.5 Ensembl:ENSG00000103495,Ensembl:ENSG00000280607 Protein coding,lincRNA CDS,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29810072..29810233 26863196 MeRIP-seq:(Medium) rs201662748 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 46 liver,large intestine Human_RBP_ID_234426,Human_RBP_ID_472116,Human_RBP_ID_893214,Human_RBP_ID_1003893,Human_RBP_ID_5097354,Human_RBP_ID_5183917,Human_RBP_ID_5247384,Human_RBP_ID_5259664,Human_RBP_ID_5495426,Human_RBP_ID_5648338,Human_RBP_ID_6506856,Human_RBP_ID_12714910,Human_RBP_ID_17874970,Human_RBP_ID_22532687,Human_RBP_ID_27441119 Human_Splice_Rec_1699968,Human_Splice_Rec_1699976,Human_Splice_Rec_1699980,Human_Splice_Rec_1700002,Human_Splice_Rec_1700008,Human_Splice_Rec_1700018,Human_Splice_Rec_1700026,Human_Splice_Rec_1700036,Human_Splice_Rec_1700044,Human_Splice_Rec_1700046,Human_Splice_Rec_1700062 RMVar_hsa_circ_26374 113020 RMVar_ID_113020 Human_SNP_ID_826644388 m1A Human chr16 - 56989591 56989591 56989591 ACTCACCCTCAGAGCTCCCGGCACTCACCCTCAGCGCTCGCGGCTCCTCCGCGCTCTGCACGAAA ACTCACCCTCAGAGCTCCCGGCACTCACCCTCGGCGCTCGCGGCTCCTCCGCGCTCTGCACGAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56989545..56989827 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 113021 RMVar_ID_113021 Human_SNP_ID_826656231 m1A Human chr16 + 88805577 88805577 88805577 CAGCATGGACACCATCGTGGGCATGCTCCACAACCGCTCCGAGACGCCCACCTTTGCCAAGGTCC CAGCATGGACACCATCGTGGGCATGCTCCACAGCCGCTCCGAGACGCCCACCTTTGCCAAGGTCC A G CDT1 Ensembl:ENSG00000167513 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88805438..88805628 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_761800,Human_RBP_ID_1005890,Human_RBP_ID_1524822,Human_RBP_ID_8811058,Human_RBP_ID_17882599 Human_Splice_Rec_1749925,Human_Splice_Rec_1749941 Human_miRNA_ID_2873876,Human_miRNA_ID_2981838 RMVar_hsa_circ_180557,RMVar_hsa_circ_116867,RMVar_hsa_circ_86282,RMVar_hsa_circ_103617,RMVar_hsa_circ_180558,RMVar_hsa_circ_180559 113022 RMVar_ID_113022 Human_SNP_ID_826656511 m1A Human chr16 + 56805564 56805564 56805564 GGGAGTCAATGTTGGTTGAGTGGGAGCAAGTGAAACAGCGAATTCTGCACACACTGCTGGCATCA GGGAGTCAATGTTGGTTGAGTGGGAGCAAGTGCAACAGCGAATTCTGCACACACTGCTGGCATCA A C NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56805501..56805667 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_44006,Human_RBP_ID_888764,Human_RBP_ID_3949253,Human_RBP_ID_4373363,Human_RBP_ID_5571818,Human_RBP_ID_9286303,Human_RBP_ID_9372860,Human_RBP_ID_18986328 Human_Splice_Rec_1715972,Human_Splice_Rec_1715980,Human_Splice_Rec_1715981,Human_Splice_Rec_1716022,Human_Splice_Rec_1716023,Human_Splice_Rec_1716064,Human_Splice_Rec_1716065,Human_Splice_Rec_1716076,Human_Splice_Rec_1716084,Human_Splice_Rec_1716085,Human_Splice_Rec_1716092,Human_Splice_Rec_1716096,Human_Splice_Rec_1716097,Human_Splice_Rec_1716134,Human_Splice_Rec_1716144,Human_Splice_Rec_1716145,Human_Splice_Rec_1716156,Human_Splice_Rec_1716160,Human_Splice_Rec_1716164,Human_Splice_Rec_1716165 RMVar_hsa_circ_17414,RMVar_hsa_circ_25462,RMVar_hsa_circ_85420,RMVar_hsa_circ_178590,RMVar_hsa_circ_178593,RMVar_hsa_circ_87593,RMVar_hsa_circ_344570,RMVar_hsa_circ_103358,RMVar_hsa_circ_77865,RMVar_hsa_circ_178594,RMVar_hsa_circ_178596,RMVar_hsa_circ_20231,RMVar_hsa_circ_343502,RMVar_hsa_circ_178592,RMVar_hsa_circ_290808,RMVar_hsa_circ_18118,RMVar_hsa_circ_127700,RMVar_hsa_circ_178595,RMVar_hsa_circ_375627,RMVar_hsa_circ_92014,RMVar_hsa_circ_178597,RMVar_hsa_circ_178598,RMVar_hsa_circ_178599 113023 RMVar_ID_113023 Human_SNP_ID_826657362 m1A Human chr16 + 74296949 74296949 74296949 GCCGGAGCTGGCAGTGCAGAAGGTGGTGGTCCACCCCCTGGTGCTGCTCAGTGTGGTGGATCATT GCCGGAGCTGGCAGTGCAGAAGGTGGTGGTCCGCCCCCTGGTGCTGCTCAGTGTGGTGGATCATT A G PSMD7 Ensembl:ENSG00000103035 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:74296851..74297000 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_4393246,Human_RBP_ID_5316707,Human_RBP_ID_8812486,Human_RBP_ID_8941370,Human_RBP_ID_9325208,Human_RBP_ID_9373202,Human_RBP_ID_17121691,Human_RBP_ID_22441112,Human_RBP_ID_23209701,Human_RBP_ID_26329212 Human_Splice_Rec_1739543,Human_Splice_Rec_1739555,Human_Splice_Rec_1739557,Human_Splice_Rec_1739571,Human_Splice_Rec_1739583 Human_miRNA_ID_2101730,Human_miRNA_ID_2107687,Human_miRNA_ID_2113626,Human_miRNA_ID_2166174,Human_miRNA_ID_2301290,Human_miRNA_ID_2304554,Human_miRNA_ID_2307819,Human_miRNA_ID_2597426,Human_miRNA_ID_2740334,Human_miRNA_ID_3040924 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 113024 RMVar_ID_113024 Human_SNP_ID_826669514 m1A Human chr16 - 57275 57275 57275 TCCTGAGGGCCCCCAGGTTTATGCTGACAGTTACTGTTGGGCATGCCTGGGGTGAGGCCACCACA TCCTGAGGGCCCCCAGGTTTATGCTGACAGTTCCTGTTGGGCATGCCTGGGGTGAGGCCACCACA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57224..57373 32194978 MeRIP-seq:(Medium) rs1045001 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine GWAS_ID_8850,GWAS_ID_8851,GWAS_ID_8852,GWAS_ID_8853,GWAS_ID_8854 113025 RMVar_ID_113025 Human_SNP_ID_826680251 m1A Human chr16 - 85779537 85779537 85779537 GCAGAATGTTCAGTCGGTCGTGTTTTTAACACAGAGTCTCTAGAAGAGGTGCAGACATCCCGTCT GCAGAATGTTCAGTCGGTCGTGTTTTTAACACGGAGTCTCTAGAAGAGGTGCAGACATCCCGTCT T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:85779380..85779629 32194978 MeRIP-seq:(Medium) rs1440723989 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_481001,Human_RBP_ID_1005787,Human_RBP_ID_1523827,Human_RBP_ID_1847475,Human_RBP_ID_12834313,Human_RBP_ID_17255548,Human_RBP_ID_17653108,Human_RBP_ID_17882164,Human_RBP_ID_18685919,Human_RBP_ID_27660920 Human_miRNA_ID_2751063,Human_miRNA_ID_2797940,Human_miRNA_ID_2798906,Human_miRNA_ID_2800287,Human_miRNA_ID_2807602,Human_miRNA_ID_2810746,Human_miRNA_ID_2813888,Human_miRNA_ID_2833478,Human_miRNA_ID_2853001,Human_miRNA_ID_2854063,Human_miRNA_ID_2861145 RMVar_hsa_circ_115833,RMVar_hsa_circ_180376,RMVar_hsa_circ_180377 113026 RMVar_ID_113026 Human_SNP_ID_826684162 m1A Human chr16 + 68357234 68357234 68357234 GGCATGCAGATACCCCAGACTGACCACTCTTGAGCAATAAAGTGGCCTGAGGGCTGGGGTTCTGA GGCATGCAGATACCCCAGACTGACCACTCTTGCGCAATAAAGTGGCCTGAGGGCTGGGGTTCTGA A C PRMT7 Ensembl:ENSG00000132600 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:68357218..68357319 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_8437115,Human_RBP_ID_12784556 Human_miRNA_ID_268534 RMVar_hsa_circ_265528 113027 RMVar_ID_113027 Human_SNP_ID_826685796 m1A Human chr16 + 70251030 70251030 70251030 ACTGGAGGCCGATGGCGCGGGTCTTTTCGTGGACGGCGGCAGCACGGTCCTCGGCTTGCGTCCGT ACTGGAGGCCGATGGCGCGGGTCTTTTCGTGGGCGGCGGCAGCACGGTCCTCGGCTTGCGTCCGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70250980..70251150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 113028 RMVar_ID_113028 Human_SNP_ID_826693427 m1A Human chr16 + 87951665 87951665 87951665 GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGATCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC GCCCCGCCGCCGCCAACCGCCCGGGCCGGGCGGTCGCCCCCCGGGCCCCGCTCCCCGTCCCCGGC A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:87951573..87951750 26863410 MeRIP-seq:(Medium) rs549143184 Functional Loss SNV ICGC 33..33 33 PBCA 2 - Human_RBP_ID_26780772 RMVar_hsa_circ_85665,RMVar_hsa_circ_180460 113029 RMVar_ID_113029 Human_SNP_ID_826694373 m1A Human chr16 + 2205813 2205812 2205813 TCCCCCCTGCCGGCTGCGGAGGTGGGGGGGGGACGGCGCCCCCGCCGTGTGCGTGGGGCGGGGAT TCCCCCCTGCCGGCTGCGGAGGTGGGGGGGGG_CGGCGCCCCCGCCGTGTGCGTGGGGCGGGGAT GA G MLST8 Ensembl:ENSG00000167965 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr16:2205767..2205875;chr16:2205768..2205869 26863196,32194978 MeRIP-seq:(Medium) rs551624542 Functional Loss DEL ICGC 33..33 33 PRAD 1 - Human_RBP_ID_4356210 Human_Splice_Rec_1664933,Human_Splice_Rec_1665133,Human_Splice_Rec_1665147,Human_Splice_Rec_1665163 113030 RMVar_ID_113030 Human_SNP_ID_826695051 m1A Human chr16 - 89686742 89686742 89686742 AGAAGCCCTCCTTACGAATACACTTCAGACGGATCTGCTCGCACTCCAGATCTGGCTCCGCCATG AGAAGCCCTCCTTACGAATACACTTCAGACGGGTCTGCTCGCACTCCAGATCTGGCTCCGCCATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:89686676..89686915;chr16:89686676..89687050;chr16:89686676..89686899 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney 113031 RMVar_ID_113031 Human_SNP_ID_826699530 m1A Human chr16 - 30893911 30893911 30893911 TGGCCGGCCGGACTGTACGGGCCGAGACCCGGAGCCGGGCCAAGGATGACATCAAGAAGGTGATG TGGCCGGCCGGACTGTACGGGCCGAGACCCGGGGCCGGGCCAAGGATGACATCAAGAAGGTGATG T C AC135048.2,BCL7C Ensembl:ENSG00000262721,Ensembl:ENSG00000099385 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:30893876..30894050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_473161,Human_RBP_ID_4393036,Human_RBP_ID_5180676,Human_RBP_ID_8941343,Human_RBP_ID_17653011 Human_Splice_Rec_1704333,Human_Splice_Rec_1704343,Human_Splice_Rec_1704353,Human_Splice_Rec_1704363 113032 RMVar_ID_113032 Human_SNP_ID_826711722 m1A Human chr16 - 72788010 72788010 72788010 AAAGACCCTGCCAAAGAATCCCCCAAACCAGAAGAACAGAAAAACACCCCCCGTGAGGTGTCCCC AAAGACCCTGCCAAAGAATCCCCCAAACCAGACGAACAGAAAAACACCCCCCGTGAGGTGTCCCC T G ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787960..72788110 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_18940531 113033 RMVar_ID_113033 Human_SNP_ID_826712953 m1A Human chr16 + 1817181 1817181 1817181 GCAGGGAGGCGCTGCCTACTGTGTCCGGGGGGAGCCGGCCCAAGACCTCCAGCAGAGCTTTACAC GCAGGGAGGCGCTGCCTACTGTGTCCGGGGGGGGCCGGCCCAAGACCTCCAGCAGAGCTTTACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1817176..1817275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 9 pancreas 113034 RMVar_ID_113034 Human_SNP_ID_826715720 m1A Human chr16 - 57518256 57518256 57518256 CCCTGCTGCAGATGGAGCGGCTGCAGGCCGAAAACGCTGCGGAGTGGGGCCGCCGGGAGCGGCTG CCCTGCTGCAGATGGAGCGGCTGCAGGCCGAATACGCTGCGGAGTGGGGCCGCCGGGAGCGGCTG T A CCDC102A Ensembl:ENSG00000135736 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:57518057..57528935 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_Splice_Rec_1718610 RMVar_hsa_circ_49103,RMVar_hsa_circ_269697,RMVar_hsa_circ_30037 113035 RMVar_ID_113035 Human_SNP_ID_826722090 m1A Human chr16 - 2234303 2234303 2234303 AGTGGACGCGCCGGTGGCCACGCACATGGGCAATGGTCTTGTAGAGCTTCCCGCAGTCGCCACAG AGTGGACGCGCCGGTGGCCACGCACATGGGCAGTGGTCTTGTAGAGCTTCCCGCAGTCGCCACAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2234252..2234353 32194978 MeRIP-seq:(Medium) rs747632415 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_1514295,Human_RBP_ID_18675053 113036 RMVar_ID_113036 Human_SNP_ID_826731278 m1A Human chr16 - 579162 579162 579162 ACCCTGCCCCATACCTGGTCCAGGTCATAGGAACAGGAGTCCACGCGCTGGCGCAGAACGTTCCA ACCCTGCCCCATACCTGGTCCAGGTCATAGGAGCAGGAGTCCACGCGCTGGCGCAGAACGTTCCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:579111..579211 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas 113037 RMVar_ID_113037 Human_SNP_ID_826762260 m1A Human chr16 - 11886574 11886574 11886574 AAGAATGTAAGGAGAAACTAGTGCCATTTTTGAAAAAAGTTGGCTTCAATCCCAAAAAGGACATT AAGAATGTAAGGAGAAACTAGTGCCATTTTTGGAAAAAGTTGGCTTCAATCCCAAAAAGGACATT T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_468281,Human_RBP_ID_1512321,Human_RBP_ID_9060050,Human_RBP_ID_17871572,Human_RBP_ID_23678470 Human_Splice_Rec_1678664,Human_Splice_Rec_1678692,Human_Splice_Rec_1678716,Human_Splice_Rec_1678738,Human_Splice_Rec_1678766,Human_Splice_Rec_1678780,Human_Splice_Rec_1678788 RMVar_hsa_circ_29325,RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_328182,RMVar_hsa_circ_346910,RMVar_hsa_circ_292356,RMVar_hsa_circ_57970,RMVar_hsa_circ_176335,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_356431,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_123824,RMVar_hsa_circ_176340,RMVar_hsa_circ_122966,RMVar_hsa_circ_291298,RMVar_hsa_circ_301376,RMVar_hsa_circ_306264,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_60859,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_337091,RMVar_hsa_circ_176337,RMVar_hsa_circ_360748,RMVar_hsa_circ_288012,RMVar_hsa_circ_176343,RMVar_hsa_circ_68557,RMVar_hsa_circ_120157,RMVar_hsa_circ_176344,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_313451,RMVar_hsa_circ_369412,RMVar_hsa_circ_176342,RMVar_hsa_circ_322195,RMVar_hsa_circ_301652,RMVar_hsa_circ_176346,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_176347 113038 RMVar_ID_113038 Human_SNP_ID_826763324 m1A Human chr16 - 31180196 31180196 31180196 CCGTTTGAGGCCATGTCCGCGCACGCGCGCACAGGCAAGCAAGCAACGAAGTTCCAACACCGCTG CCGTTTGAGGCCATGTCCGCGCACGCGCGCACGGGCAAGCAAGCAACGAAGTTCCAACACCGCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31180151..31180350 26863196 MeRIP-seq:(Medium) rs1567467403 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 113039 RMVar_ID_113039 Human_SNP_ID_826774179 m1A Human chr16 - 71722912 71722912 71722912 GAGAAGTAAGTTTACGAAGGAATGCACAAGGTAGGGTGGCGATAGTGGGGAGGAGAAGATGGTTA GAGAAGTAAGTTTACGAAGGAATGCACAAGGTGGGGTGGCGATAGTGGGGAGGAGAAGATGGTTA T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:71722909..71723206 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 113040 RMVar_ID_113040 Human_SNP_ID_826777676 m1A Human chr16 + 30429152 30429152 30429152 AACTGTTCCCAGTCTCGTTCCGCAGCAAACTCAGCATGGAGGCGGCGGCTGAAATAGGACAAAGG AACTGTTCCCAGTCTCGTTCCGCAGCAAACTCGGCATGGAGGCGGCGGCTGAAATAGGACAAAGG A G ZNF771 Ensembl:ENSG00000179965 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30429101..30429207;chr16:30429101..30429175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 2 - 113041 RMVar_ID_113041 Human_SNP_ID_826779456 m1A Human chr16 + 70158560 70158558 70158561 ACCACTCCTAGTGATTACTGACTTTAGTGCCTAAACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA ACCACTCCTAGTGATTACTGACTTTAGTGCC___ACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA CTAA C PDPR Ensembl:ENSG00000090857 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1567569975 Functional Loss DEL ICGC 32..34 33 SKCA 1 - Human_RBP_ID_18287002 Human_miRNA_ID_736151 RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 113042 RMVar_ID_113042 Human_SNP_ID_826794147 m1A Human chr16 - 16102719 16102719 16102719 GTCCTTAGGTTGGGGCCTTCCTCCCCGCCCTTACCTCTGCAGTTGCTTCCCTGCACTGTCCGTCA GTCCTTAGGTTGGGGCCTTCCTCCCCGCCCTTGCCTCTGCAGTTGCTTCCCTGCACTGTCCGTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:16102677..16102776 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113043 RMVar_ID_113043 Human_SNP_ID_826794742 m1A Human chr16 - 22195740 22195740 22195740 TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGATGGCGTGGGTTCGAATCCCACCGCTGCCACAC TAAGGCGCTGGATTTAGGCTCCAGTCATTTCGGTGGCGTGGGTTCGAATCCCACCGCTGCCACAC T C tRNA-Leu-TAG-3-1 RNACentral:URS000005AEAB tRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:22195710..22195784 26863196 MeRIP-seq:(Medium) rs1484017196 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_277312,Human_RBP_ID_470365,Human_RBP_ID_1003413,Human_RBP_ID_1131254,Human_RBP_ID_1177312,Human_RBP_ID_1281299,Human_RBP_ID_1365199,Human_RBP_ID_1514089,Human_RBP_ID_1839443,Human_RBP_ID_3492634,Human_RBP_ID_4397069,Human_RBP_ID_5097606,Human_RBP_ID_5259115,Human_RBP_ID_5274748,Human_RBP_ID_5289863,Human_RBP_ID_5440236,Human_RBP_ID_5464788,Human_RBP_ID_5495261,Human_RBP_ID_5536097,Human_RBP_ID_6499986,Human_RBP_ID_8251998,Human_RBP_ID_8429516,Human_RBP_ID_8805513,Human_RBP_ID_9060914,Human_RBP_ID_9284451,Human_RBP_ID_12688447,Human_RBP_ID_17253322,Human_RBP_ID_17369013,Human_RBP_ID_17485450,Human_RBP_ID_17582529,Human_RBP_ID_17587143,Human_RBP_ID_17689828,Human_RBP_ID_17873269,Human_RBP_ID_18174157,Human_RBP_ID_18178525,Human_RBP_ID_18199848,Human_RBP_ID_18207363,Human_RBP_ID_18437270,Human_RBP_ID_18529669,Human_RBP_ID_18674881,Human_RBP_ID_20102941,Human_RBP_ID_21926765,Human_RBP_ID_22497372,Human_RBP_ID_22802929,Human_RBP_ID_22936658,Human_RBP_ID_23110392,Human_RBP_ID_23111459,Human_RBP_ID_23127966,Human_RBP_ID_23682595,Human_RBP_ID_24477477,Human_RBP_ID_24538744,Human_RBP_ID_25197064,Human_RBP_ID_26446513,Human_RBP_ID_26748903,Human_RBP_ID_26940189,Human_RBP_ID_27155803,Human_RBP_ID_27238494,Human_RBP_ID_27439975,Human_RBP_ID_27657285 113044 RMVar_ID_113044 Human_SNP_ID_826796053 m1A Human chr16 - 18926008 18926008 18926008 TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCAGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG TGAGCCGCAGAGCCCCGGGGTCTCGGCTGAGCGGCGGCGGCGGCGGCGGCGGCACCAAGTATCCG T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:18925959..18926367 26863196 MeRIP-seq:(Medium) rs190057031 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,colon adenocarcinoma,meninges rhabdoid,large_intestine adenocarcinoma,kidney papillary_renal_cell_carcinoma 10 kidney,stomach,large intestine,brain Human_RBP_ID_234950,Human_RBP_ID_762716,Human_RBP_ID_5524195,Human_RBP_ID_9286164 Human_Splice_Rec_1685185,Human_Splice_Rec_1685547,Human_Splice_Rec_1685585 113045 RMVar_ID_113045 Human_SNP_ID_826798278 m1A Human chr16 - 30711875 30711872 30711876 GCTGAACTTCCACTTGTTTCTTCCTCCTCTGAATGTTCATCTTCCTCATCCTCACTCCGGTCCTC GCTGAACTTCCACTTGTTTCTTCCTCCTCTG____TTCATCTTCCTCATCCTCACTCCGGTCCTC ACATT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30711551..30712092 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..35 33 BRCA 1 - 113046 RMVar_ID_113046 Human_SNP_ID_826798725 m1A Human chr16 - 30370348 30370348 30370348 TCGAGAGAGACCCCGGCGCGCGGCGCCCCCCGACCCCTGCCCCGCCTCTGCGCGCCCAGCGGCCG TCGAGAGAGACCCCGGCGCGCGGCGCCCCCCGCCCCCTGCCCCGCCTCTGCGCGCCCAGCGGCCG T G TBC1D10B Ensembl:ENSG00000169221 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972533,GSM1972534 HEK293T,Wild Type;HEPG2 cell line,total RNA Untreated chr16:30370101..30370400;chr16:30370257..30370417 26863410,26863196 MeRIP-seq:(Medium) rs976655830 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 113047 RMVar_ID_113047 Human_SNP_ID_826805020 m1A Human chr16 - 31493526 31493526 31493526 ACTGCCTAGGCATCCTGACCCCAGCTTCCCACAGGTTTCTGGCCAGCTCCGTCTCTATCCCTGGG ACTGCCTAGGCATCCTGACCCCAGCTTCCCACGGGTTTCTGGCCAGCTCCGTCTCTATCCCTGGG T C C16orf58 Ensembl:ENSG00000140688 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:31493480..31493581 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_3947628,Human_RBP_ID_19071497 Human_Splice_Rec_1706379,Human_Splice_Rec_1706403,Human_Splice_Rec_1706433,Human_Splice_Rec_1706459 RMVar_hsa_circ_11795,RMVar_hsa_circ_299524,RMVar_hsa_circ_59505,RMVar_hsa_circ_101404,RMVar_hsa_circ_116899,RMVar_hsa_circ_178057,RMVar_hsa_circ_120741,RMVar_hsa_circ_178058,RMVar_hsa_circ_178059 113048 RMVar_ID_113048 Human_SNP_ID_826806598 m1A Human chr16 + 8859327 8859327 8859327 GGGGCTGTGGTGGTGGGGGAGGCTCAGATGACATGGCTGACCTGGAAAGAGAAGAGGCTGTCAGG GGGGCTGTGGTGGTGGGGGAGGCTCAGATGACGTGGCTGACCTGGAAAGAGAAGAGGCTGTCAGG A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:8859140..8859350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_3506925,Human_RBP_ID_5573648,Human_RBP_ID_8188818,Human_RBP_ID_12853816,Human_RBP_ID_22355947,Human_RBP_ID_22713017 113049 RMVar_ID_113049 Human_SNP_ID_826817448 m1A Human chr16 - 2246975 2246975 2246975 TCTTCTCATTCTTTAAATTAGGGGTCGCTGTGATGAAATTCAAGAACCCCCCAGTGAACAGCCTG TCTTCTCATTCTTTAAATTAGGGGTCGCTGTGGTGAAATTCAAGAACCCCCCAGTGAACAGCCTG T C ECI1 Ensembl:ENSG00000167969 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:2246901..2247094 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_RBP_ID_3948594,Human_RBP_ID_4393505,Human_RBP_ID_17123719,Human_RBP_ID_18675106,Human_RBP_ID_18985235,Human_RBP_ID_22440822 Human_Splice_Rec_1665404,Human_Splice_Rec_1665416,Human_Splice_Rec_1665428,Human_Splice_Rec_1665438,Human_Splice_Rec_1665452,Human_Splice_Rec_1665460 RMVar_hsa_circ_91147,RMVar_hsa_circ_175727,RMVar_hsa_circ_175725,RMVar_hsa_circ_335660 113050 RMVar_ID_113050 Human_SNP_ID_826840626 m1A Human chr16 - 4506863 4506863 4506863 TCTGTGGAGAGATGGGAGGTGTTTGTGTGTCAATTAGCCCTTCCCAGCTTTCCAGAAAGGACCAT TCTGTGGAGAGATGGGAGGTGTTTGTGTGTCAGTTAGCCCTTCCCAGCTTTCCAGAAAGGACCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:4506861..4506975 26863196 MeRIP-seq:(Medium) rs775285965 Functional Loss SNV ICGC 33..33 33 STAD 1 - 113051 RMVar_ID_113051 Human_SNP_ID_826857426 m1A Human chr16 - 30925809 30925809 30925809 CTCAGTTCGCACACAGGCCCGGCAGCGGCGGCAGCGGGTTCGGCGTCGGCGCGCTCCGGCCCCCG CTCAGTTCGCACACAGGCCCGGCAGCGGCGGCGGCGGGTTCGGCGTCGGCGCGCTCCGGCCCCCG T C FBXL19-AS1 RNACentral:URS00009B83FC lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:30925710..30925824 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 113052 RMVar_ID_113052 Human_SNP_ID_826857946 m1A Human chr16 - 31109549 31109549 31109549 ACCAGAAGGTGGCTGCCGTCCTGAGAGCGGCCAGCGTAGAGCATCATGGTGGGCGTTAGGCGGAC ACCAGAAGGTGGCTGCCGTCCTGAGAGCGGCCGGCGTAGAGCATCATGGTGGGCGTTAGGCGGAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31109408..31109842 32194978 MeRIP-seq:(Medium) rs777686530 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 113053 RMVar_ID_113053 Human_SNP_ID_826866825 m1A Human chr16 + 3113439 3113439 3113439 TTCTTTCTAGCTCTGAAATAGAAAATGTCTGCAGACGGCGGAGGCATCCAGGACACCCAGGACAA TTCTTTCTAGCTCTGAAATAGAAAATGTCTGCGGACGGCGGAGGCATCCAGGACACCCAGGACAA A G ZNF205 Ensembl:ENSG00000122386 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:3113356..3113440 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_1669094,Human_Splice_Rec_1669095,Human_Splice_Rec_1669106,Human_Splice_Rec_1669107,Human_Splice_Rec_1669118,Human_Splice_Rec_1669119,Human_Splice_Rec_1669130,Human_Splice_Rec_1669131,Human_Splice_Rec_1669136,Human_Splice_Rec_1669137 RMVar_hsa_circ_83505,RMVar_hsa_circ_175843,RMVar_hsa_circ_337452 113054 RMVar_ID_113054 Human_SNP_ID_826867955 m1A Human chr16 + 83808684 83808684 83808684 CGTGTTTGTTTGTTTCGGTTTTTCTTAGGTGCAGACACTCCTGCAGCAGATGCAAGATAAATTTC CGTGTTTGTTTGTTTCGGTTTTTCTTAGGTGCGGACACTCCTGCAGCAGATGCAAGATAAATTTC A G HSBP1 Ensembl:ENSG00000230989 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83808676..83809215 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_762312,Human_RBP_ID_890742,Human_RBP_ID_4394024,Human_RBP_ID_8440165,Human_RBP_ID_22441137,Human_RBP_ID_25240787 Human_Splice_Rec_1745106,Human_Splice_Rec_1745110 Human_miRNA_ID_1960894 RMVar_hsa_circ_180249,RMVar_hsa_circ_105491,RMVar_hsa_circ_180248,RMVar_hsa_circ_101469,RMVar_hsa_circ_371076,RMVar_hsa_circ_180250 113055 RMVar_ID_113055 Human_SNP_ID_826878648 m1A Human chr16 + 2765733 2765733 2765733 CGGAGAAGTCCCTCAGTGTCTTCCCCGGAGCCAGCCGAAAAATCGAGGTCTTCACGCCGACGGCG CGGAGAAGTCCCTCAGTGTCTTCCCCGGAGCCGGCCGAAAAATCGAGGTCTTCACGCCGACGGCG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2765683..2765848 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_45338,Human_RBP_ID_234058,Human_RBP_ID_471564,Human_RBP_ID_1365388,Human_RBP_ID_1515636,Human_RBP_ID_1840768,Human_RBP_ID_3493707,Human_RBP_ID_5182473,Human_RBP_ID_8431155,Human_RBP_ID_17669551,Human_RBP_ID_18676578,Human_RBP_ID_20093664 Human_miRNA_ID_2083919 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 113056 RMVar_ID_113056 Human_SNP_ID_826879103 m1A Human chr16 - 57451179 57451179 57451179 TACCTGGGGGGTGAATGAGAAGACTCTGGATCAGGTTTTTCTGCCCCCTGTGTCTCAGAATGCTG TACCTGGGGGGTGAATGAGAAGACTCTGGATCGGGTTTTTCTGCCCCCTGTGTCTCAGAATGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57450999..57451242 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 113057 RMVar_ID_113057 Human_SNP_ID_826884097 m1A Human chr16 - 1772606 1772606 1772606 CCACGGGAAGGCCTGGGGCATCCTGACCTTCAAAGGTAAGGCTCGGGAGAGCGGGTGCCCGGCAG CCACGGGAAGGCCTGGGGCATCCTGACCTTCAGAGGTAAGGCTCGGGAGAGCGGGTGCCCGGCAG T C MRPS34 Ensembl:ENSG00000074071 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:1772601..1772650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_889283,Human_RBP_ID_4352768,Human_RBP_ID_19070489,Human_RBP_ID_22799993,Human_RBP_ID_23256401,Human_RBP_ID_23680950,Human_RBP_ID_26939101 Human_Splice_Rec_1660476,Human_Splice_Rec_1660477,Human_Splice_Rec_1660480,Human_Splice_Rec_1660481,Human_Splice_Rec_1660483 113058 RMVar_ID_113058 Human_SNP_ID_826892513 m1A Human chr16 + 85579970 85579970 85579970 AAAAGACAAAAATCCTGGAGCGGCTGGAACTGACTTAGTAGTTAGAGAGGCAGACAGTAGACAAG AAAAGACAAAAATCCTGGAGCGGCTGGAACTGCCTTAGTAGTTAGAGAGGCAGACAGTAGACAAG A C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:85579960..85580140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_8440699 113059 RMVar_ID_113059 Human_SNP_ID_826892702 m1A Human chr16 - 28845998 28845998 28845998 CCGCGGCCTGGCCGTGGAGGCCAAGAAGACTTACGTGCGCGACAAGCCACATGTGAATGTGGGTA CCGCGGCCTGGCCGTGGAGGCCAAGAAGACTTTCGTGCGCGACAAGCCACATGTGAATGTGGGTA T A TUFM Ensembl:ENSG00000178952 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28845976..28846325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_46351,Human_RBP_ID_471865,Human_RBP_ID_1516027,Human_RBP_ID_4360963,Human_RBP_ID_8811838,Human_RBP_ID_9286226,Human_RBP_ID_9372590,Human_RBP_ID_18207376,Human_RBP_ID_22800772,Human_RBP_ID_26942042,Human_RBP_ID_27239923,Human_RBP_ID_27441033 Human_Splice_Rec_1698091,Human_Splice_Rec_1698113 113060 RMVar_ID_113060 Human_SNP_ID_826893562 m1A Human chr16 + 70346952 70346952 70346952 GCGAGGTTAGGGCCCGCGTTGCGACGTGGTGCAGCGCATATTTTCACAAGTGGGTCTCCCTTGTC GCGAGGTTAGGGCCCGCGTTGCGACGTGGTGCTGCGCATATTTTCACAAGTGGGTCTCCCTTGTC A T DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:70346901..70347050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney Human_RBP_ID_234106,Human_RBP_ID_761935,Human_RBP_ID_895506,Human_RBP_ID_4393964,Human_RBP_ID_9326051 Human_Splice_Rec_1735109,Human_Splice_Rec_1735119,Human_Splice_Rec_1735123,Human_Splice_Rec_1735143,Human_Splice_Rec_1735151,Human_Splice_Rec_1735161,Human_Splice_Rec_1735183,Human_Splice_Rec_1735193,Human_Splice_Rec_1735203,Human_Splice_Rec_1735223 RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 113061 RMVar_ID_113061 Human_SNP_ID_826900156 m1A Human chr16 - 21953417 21953417 21953417 GAGCCGGCTCTGGTTAGTAGCTTCATGATTCAAGATTGTTCTGACACACGGTCACTGCCGGATTA GAGCCGGCTCTGGTTAGTAGCTTCATGATTCATGATTGTTCTGACACACGGTCACTGCCGGATTA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:21953351..21957325;chr16:21953326..21957325;chr16:21953351..21953506 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 5 haematopoietic and lymphoid tissue 113062 RMVar_ID_113062 Human_SNP_ID_826920350 m1A Human chr16 + 1961648 1961648 1961648 CCAAGGCCTACCAGGACCGCTGTGCGTGCCCCACCCACCCCCAACCCCCCACCATCCTCCTGAGG CCAAGGCCTACCAGGACCGCTGTGCGTGCCCCCCCCACCCCCAACCCCCCACCATCCTCCTGAGG A C NDUFB10 Ensembl:ENSG00000140990 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs762609751 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_23681817 Human_miRNA_ID_1418542 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_175582 113063 RMVar_ID_113063 Human_SNP_ID_826920474 m1A Human chr16 - 86568751 86568751 86568751 GATCTGTAGGGCAGCTGGCAGCTGGCATTGCCACTCACCTGGGACTCCCCGAGGGTCGAGTTCTC GATCTGTAGGGCAGCTGGCAGCTGGCATTGCCGCTCACCTGGGACTCCCCGAGGGTCGAGTTCTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:86568703..86568863 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 113064 RMVar_ID_113064 Human_SNP_ID_826921184 m1A Human chr16 - 88726800 88726800 88726800 CTACCTGCTGCTCTTCGGCACGGCCCTGCTGCAGAGGGACACACGGGCCCGCCTCGTGCTGTGGG CTACCTGCTGCTCTTCGGCACGGCCCTGCTGCGGAGGGACACACGGGCCCGCCTCGTGCTGTGGG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr16:88726751..88726800 26863196,32194978 MeRIP-seq:(Medium) rs1203783140 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_22532860 Human_Splice_Rec_1749753 Human_miRNA_ID_2956300 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_315316 113065 RMVar_ID_113065 Human_SNP_ID_826924012 m1A Human chr16 + 31093407 31093407 31093407 TGTCCTGTCCCAGCACATGCTCCACCAGCCCGAAACCCCTGCCCCACCTGGCAGAGGGGTGGGGT TGTCCTGTCCCAGCACATGCTCCACCAGCCCGGAACCCCTGCCCCACCTGGCAGAGGGGTGGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31093358..31093470 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - 113066 RMVar_ID_113066 Human_SNP_ID_826924454 m1A Human chr16 - 88534510 88534510 88534510 TCGGGGGGCAGTAGGGGCAGGCGGCGGCGGGCAGGCCGAGCGCGCCGGGCGGTGGCGCAGCGGGG TCGGGGGGCAGTAGGGGCAGGCGGCGGCGGGCGGGCCGAGCGCGCCGGGCGGTGGCGCAGCGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:88534283..88534682 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 113067 RMVar_ID_113067 Human_SNP_ID_826930299 m1A Human chr16 + 80795627 80795627 80795627 GAAGTGCTACTCCACAACCCCCACCATTCACCAACCTACCAGAGCCAGGGGCTGACTCCAGACAA GAAGTGCTACTCCACAACCCCCACCATTCACCCACCTACCAGAGCCAGGGGCTGACTCCAGACAA A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:80795533..80795646 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113068 RMVar_ID_113068 Human_SNP_ID_826935286 m1A Human chr16 - 494827 494827 494827 TGATCCTCCCACCTCTGCAGCCTCGACCTCCCAGGCTCATGTGATCCTCCCACCTCTGCAGCCTC TGATCCTCCCACCTCTGCAGCCTCGACCTCCCCGGCTCATGTGATCCTCCCACCTCTGCAGCCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:494642..495289 26863196 MeRIP-seq:(Medium) rs4984880 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 113069 RMVar_ID_113069 Human_SNP_ID_826938848 m1A Human chr16 + 2763475 2763475 2763475 CCTCCTCACCAGATACCAAAGTGAAACCTGAAACACCGCCAAGACAAAGTCACTCAGGGTCTATT CCTCCTCACCAGATACCAAAGTGAAACCTGAAGCACCGCCAAGACAAAGTCACTCAGGGTCTATT A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:2763451..2763475 26863196 MeRIP-seq:(Medium) rs1238322919 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_1515535,Human_RBP_ID_1840705,Human_RBP_ID_3493664,Human_RBP_ID_8431061,Human_RBP_ID_12708979,Human_RBP_ID_17255830,Human_RBP_ID_18676468,Human_RBP_ID_27239677 Human_miRNA_ID_2376748 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 113070 RMVar_ID_113070 Human_SNP_ID_826950700 m1A Human chr16 - 2036436 2036433 2036437 GGGCGGCAGGTGAGCCCGGGTCCACAGAGCGGATGTACTGGCCGGGCCGGGACTTGTCACTATGC GGGCGGCAGGTGAGCCCGGGTCCACAGAGCG____TACTGGCCGGGCCGGGACTTGTCACTATGC ACATC A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2036389..2036537 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..35 33 STAD 1 - 113071 RMVar_ID_113071 Human_SNP_ID_826954679 m1A Human chr16 - 86578844 86578844 86578844 GGGAGGCTTCTGCGGGGTCTCGGCCCGGCCCGAGGCAGCTAGAGCAGCCGCGGGGGCGAAGGCCA GGGAGGCTTCTGCGGGGTCTCGGCCCGGCCCGCGGCAGCTAGAGCAGCCGCGGGGGCGAAGGCCA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:86578720..86579017 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 1 pancreas 113072 RMVar_ID_113072 Human_SNP_ID_826959349 m1A Human chr16 - 29808295 29808295 29808295 TGAAAACCAAGACAGGAGGAGGCGGGCTTCCTACCTCACATTTGAAGGGCCGTTCTGTTGAGTGC TGAAAACCAAGACAGGAGGAGGCGGGCTTCCTCCCTCACATTTGAAGGGCCGTTCTGTTGAGTGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:29808276..29808300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 12 kidney RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_177760 113073 RMVar_ID_113073 Human_SNP_ID_826963391 m1A Human chr16 - 31459201 31459201 31459201 CCTCCAGGTGGGCCAGGGCCTCCGAACAGCCCAGAAGTCCGACCACGGAGCCTTCGTGCCGTGCC CCTCCAGGTGGGCCAGGGCCTCCGAACAGCCCTGAAGTCCGACCACGGAGCCTTCGTGCCGTGCC T A AC026471.1 Ensembl:ENSG00000260267 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:31459061..31459230 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 11 pancreas Human_RBP_ID_235286,Human_RBP_ID_4367015,Human_RBP_ID_5575790 113074 RMVar_ID_113074 Human_SNP_ID_826966504 m1A Human chr16 - 30652938 30652938 30652938 GAGGTCCGGTGGATGCGGCTCAAGGGCTCGCGACACAAACACAGAGGGTCGGGAGGCCTAGCGAG GAGGTCCGGTGGATGCGGCTCAAGGGCTCGCGGCACAAACACAGAGGGTCGGGAGGCCTAGCGAG T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr16:30652820..30652994;chr16:30652823..30652939 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113075 RMVar_ID_113075 Human_SNP_ID_826972094 m1A Human chr16 - 288156 288156 288156 AGAGGACGAGGCCGTCCTGCCCGTCTTTGAGGAGAAGATCATCGGCAAAGTGGAGAAGGTGGACT AGAGGACGAGGCCGTCCTGCCCGTCTTTGAGGGGAAGATCATCGGCAAAGTGGAGAAGGTGGACT T C AXIN1 Ensembl:ENSG00000103126 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:288001..288251 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_44205,Human_RBP_ID_473674,Human_RBP_ID_1066172,Human_RBP_ID_3946856,Human_RBP_ID_5114054 Human_Splice_Rec_1653546,Human_Splice_Rec_1653566,Human_Splice_Rec_1653584 RMVar_hsa_circ_175313,RMVar_hsa_circ_84104,RMVar_hsa_circ_112153,RMVar_hsa_circ_85828,RMVar_hsa_circ_175315,RMVar_hsa_circ_76323,RMVar_hsa_circ_175316,RMVar_hsa_circ_175314 113076 RMVar_ID_113076 Human_SNP_ID_826972638 m1A Human chr16 - 68235993 68235993 68235993 GCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGACCCCGCCGCGGACCCCTGCCCCTGGCCCGGAT GCCCCCTCCCCCGGGCCCTGACCCCGCGGCCGCCCCCGCCGCGGACCCCTGCCCCTGGCCCGGAT T G ESRP2 Ensembl:ENSG00000103067 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:68235837..68236100 26863196 MeRIP-seq:(Medium) rs1018552761 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4378844,Human_RBP_ID_18419077 113077 RMVar_ID_113077 Human_SNP_ID_826973446 m1A Human chr16 - 2975731 2975731 2975731 CACCATTCCGGGGCCCCAAGGACCGGGCCCGCAAGTTGGCCGAGGTGGGCAGCCACGAGAAGGTG CACCATTCCGGGGCCCCAAGGACCGGGCCCGCCAGTTGGCCGAGGTGGGCAGCCACGAGAAGGTG T G PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2975650..2975735 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_46164,Human_RBP_ID_234828,Human_RBP_ID_261385,Human_RBP_ID_889376,Human_RBP_ID_4363068,Human_RBP_ID_5113841,Human_RBP_ID_18418645,Human_RBP_ID_21972270,Human_RBP_ID_22944969,Human_RBP_ID_24476110,Human_RBP_ID_26328046,Human_RBP_ID_26942724 Human_Splice_Rec_1667816,Human_Splice_Rec_1667836,Human_Splice_Rec_1667856,Human_Splice_Rec_1667882,Human_Splice_Rec_1667898,Human_Splice_Rec_1667914,Human_Splice_Rec_1667928,Human_Splice_Rec_1667944,Human_Splice_Rec_1667952,Human_Splice_Rec_1667958,Human_Splice_Rec_1667964 113078 RMVar_ID_113078 Human_SNP_ID_826975474 m1A Human chr16 + 66934065 66934065 66934065 GGATGCTCCGGGTCATTGATGGAGCGAATCAGATGTGGGAAGTGAAGGAAAAGGGACTCTGCGCC GGATGCTCCGGGTCATTGATGGAGCGAATCAGTTGTGGGAAGTGAAGGAAAAGGGACTCTGCGCC A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:66933738..66934131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 113079 RMVar_ID_113079 Human_SNP_ID_826975811 m1A Human chr16 - 54285501 54285501 54285501 CTTCTACCCGTATGGCCAGTACCAGTTCGGGGACCCGTCCCGTCCCAAGAACGCCACCAGGGAGA CTTCTACCCGTATGGCCAGTACCAGTTCGGGGGCCCGTCCCGTCCCAAGAACGCCACCAGGGAGA T C IRX3 Ensembl:ENSG00000177508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:54285454..54285545;chr16:54285453..54285543;chr16:54285451..54285554 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - 113080 RMVar_ID_113080 Human_SNP_ID_826990489 m1A Human chr16 - 57996745 57996745 57996745 TACGCGTCAGACCTGCAGCGGCACCGGCGGGTACACACAGGCGAGAAGCCCTACAAGTGCCCCAA TACGCGTCAGACCTGCAGCGGCACCGGCGGGTGCACACAGGCGAGAAGCCCTACAAGTGCCCCAA T C ZNF319 Ensembl:ENSG00000166188 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:57996505..57996755 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_27443607 113081 RMVar_ID_113081 Human_SNP_ID_826991095 m1A Human chr16 + 72787719 72787719 72787719 TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCCGCCACTGCCACCGCCGCC TGGTACGAGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACTGCCACCGCCGCC A G AC004943.2 Ensembl:ENSG00000259768 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:72787431..72787729 26863196 MeRIP-seq:(Medium) rs112443847 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,chest squamous_cell_carcinoma,colon adenocarcinoma,lung adenocarcinoma,brain oligodendroglioma,skin squamous_cell_carcinoma,stomach intestinal_adenocarcinoma,prostate adenocarcinoma,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,LAML,large_intestine adenocarcinoma,kidney papillary_renal_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,central_nervous_system oligodendroglioma,breast adenosis 84 lung,kidney,biliary tract,chest,gallbladder,skin,stomach,prostate,large intestine,haematopoietic and lymphoid tissue,brain,breast Human_RBP_ID_9325207 113082 RMVar_ID_113082 Human_SNP_ID_827000245 m1A Human chr16 + 790769 790769 790769 GATTTTTGCACAGCCAATCCACTGGGCCTCGGAGACGGAGTGGGCTCTGGTTTGCCCTTTTGAGT GATTTTTGCACAGCCAATCCACTGGGCCTCGGGGACGGAGTGGGCTCTGGTTTGCCCTTTTGAGT A G CHTF18 Ensembl:ENSG00000127586 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3765266 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22052700 GWAS_ID_8855,GWAS_ID_8856,GWAS_ID_8857,GWAS_ID_8858,GWAS_ID_8859,GWAS_ID_8860 RMVar_hsa_circ_95827,RMVar_hsa_circ_269155,RMVar_hsa_circ_175446 113083 RMVar_ID_113083 Human_SNP_ID_827001310 m1A Human chr16 - 11915623 11915623 11915623 CAGCAGCGACTCGGCGCCTGACTGCTGGGACCAGGCGGACATGGAAGCCCCCGGGCCGGGCCCTT CAGCAGCGACTCGGCGCCTGACTGCTGGGACCGGGCGGACATGGAAGCCCCCGGGCCGGGCCCTT T C GSPT1 Ensembl:ENSG00000103342 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:11915574..11915677 32194978 MeRIP-seq:(Medium) rs1274210487 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1512376,Human_RBP_ID_6493584,Human_RBP_ID_12667533,Human_RBP_ID_18673057,Human_RBP_ID_22441300,Human_RBP_ID_27155762,Human_RBP_ID_27439042 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 113084 RMVar_ID_113084 Human_SNP_ID_827006798 m1A Human chr16 + 3283898 3283898 3283898 GAAGCTGGAGGAGGACTGCGCCTGGAGCCAGGAGCTGCCCCCACCTGACCCAGGACCGAGCCCCG GAAGCTGGAGGAGGACTGCGCCTGGAGCCAGGGGCTGCCCCCACCTGACCCAGGACCGAGCCCCG A G ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:3283461..3284154 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine Human_RBP_ID_234534,Human_RBP_ID_9286074 113085 RMVar_ID_113085 Human_SNP_ID_827009374 m1A Human chr16 + 29807774 29807774 29807774 GGACCGCATGAGCTACCACGTGCGCTCACATGACGGCGCTGTGCACAAGCCCTACAACTGCTCCC GGACCGCATGAGCTACCACGTGCGCTCACATGCCGGCGCTGTGCACAAGCCCTACAACTGCTCCC A C MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:29807726..29807775 26863196 MeRIP-seq:(Medium) rs1468996543 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 7 head and neck Human_RBP_ID_472094,Human_RBP_ID_761114,Human_RBP_ID_1003880,Human_RBP_ID_1516230,Human_RBP_ID_1841117,Human_RBP_ID_3493991,Human_RBP_ID_4398466,Human_RBP_ID_5259189,Human_RBP_ID_6506827,Human_RBP_ID_8431761,Human_RBP_ID_8806725,Human_RBP_ID_12714855,Human_RBP_ID_17253844,Human_RBP_ID_17486022,Human_RBP_ID_18677190,Human_RBP_ID_26942277,Human_RBP_ID_27240061,Human_RBP_ID_27441113 Human_Splice_Rec_1699963,Human_Splice_Rec_1699971,Human_Splice_Rec_1699991,Human_Splice_Rec_1700003,Human_Splice_Rec_1700009,Human_Splice_Rec_1700013 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 113086 RMVar_ID_113086 Human_SNP_ID_827013092 m1A Human chr16 - 23683898 23683898 23683898 GGGCAGTGGGATCTGTCTGAAGCATCTTCTGGATGAGGGAGGCGGCCACGGGGTTGATGTGCTGG GGGCAGTGGGATCTGTCTGAAGCATCTTCTGGCTGAGGGAGGCGGCCACGGGGTTGATGTGCTGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:23683876..23683900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 113087 RMVar_ID_113087 Human_SNP_ID_827016166 m1A Human chr16 - 10942252 10942252 10942252 CACGAGGGAGCCGGGCAGCCGCGGGCCACTTCAGGGGGGCCCGCCTCGCCGCCCGGGCGGTCGAG CACGAGGGAGCCGGGCAGCCGCGGGCCACTTCGGGGGGGCCCGCCTCGCCGCCCGGGCGGTCGAG T C DEXI Ensembl:ENSG00000182108 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:10942201..10942394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4392868,Human_RBP_ID_8941326,Human_RBP_ID_17653297,Human_RBP_ID_26937983 Human_miRNA_ID_2295897,Human_miRNA_ID_2452624 RMVar_hsa_circ_124032,RMVar_hsa_circ_176222 113088 RMVar_ID_113088 Human_SNP_ID_827021007 m1A Human chr16 - 30535124 30535124 30535124 TGAAGTCCGATTATAAAAAGGTCCAGAGACGAAAACTAACTTCTGAGTTCACGAGGGCTGCCTTC TGAAGTCCGATTATAAAAAGGTCCAGAGACGATAACTAACTTCTGAGTTCACGAGGGCTGCCTTC T A ZNF747 Ensembl:ENSG00000169955 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30535096..30535246 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - 113089 RMVar_ID_113089 Human_SNP_ID_827023241 m1A Human chr16 + 67029432 67029432 67029432 GCGGGAAGATGCCGCGCGTCGTGCCCGACCAGAGAAGCAAGTTCGAGAACGAGGAGTTTTTTAGG GCGGGAAGATGCCGCGCGTCGTGCCCGACCAGGGAAGCAAGTTCGAGAACGAGGAGTTTTTTAGG A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67029101..67030042 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast HER-positive_carcinoma 3 breast Human_RBP_ID_233123,Human_RBP_ID_815970,Human_RBP_ID_892266,Human_RBP_ID_4393174,Human_RBP_ID_6525881,Human_RBP_ID_18986463,Human_RBP_ID_23695487 Human_Splice_Rec_1725145,Human_Splice_Rec_1725155,Human_Splice_Rec_1725165,Human_Splice_Rec_1725171,Human_Splice_Rec_1725183,Human_Splice_Rec_1725193 Human_miRNA_ID_3118551 RMVar_hsa_circ_179018,RMVar_hsa_circ_99066,RMVar_hsa_circ_118127,RMVar_hsa_circ_179019 113090 RMVar_ID_113090 Human_SNP_ID_827028942 m1A Human chr16 + 67438475 67438473 67438475 GACCACATACACACACACGCACACACACGCGCACACACACACACACACACACAAAGAGTGCAATT GACCACATACACACACACGCACACACACGCG__CACACACACACACACACACAAAGAGTGCAATT GCA G NONHSAG019743.2 RNACentral:URS00009BC955 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67438425..67438502 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 STAD 3 - 113091 RMVar_ID_113091 Human_SNP_ID_827038512 m1A Human chr16 + 4336948 4336948 4336948 CACGAGCAGCAAGAGCTCCTGCAGCTGCGCCCACCCCCCAAGCCGCCACTGCCCGCCCCCGACGG CACGAGCAGCAAGAGCTCCTGCAGCTGCGCCCCCCCCCCAAGCCGCCACTGCCCGCCCCCGACGG A C GLIS2 Ensembl:ENSG00000126603 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4336897..4337015 26863196 MeRIP-seq:(Medium) rs994806881 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_miRNA_ID_2457903,Human_miRNA_ID_2462826,Human_miRNA_ID_2635468,Human_miRNA_ID_2638155,Human_miRNA_ID_2873762,Human_miRNA_ID_2981725 RMVar_hsa_circ_86042,RMVar_hsa_circ_175976 113092 RMVar_ID_113092 Human_SNP_ID_827040828 m1A Human chr16 - 1962458 1962458 1962458 GGTCCACACATGGGGCATAGCCATGGTCTCTCAGCTCCGCTTAACCACACGGGTCCAGTGTGTGC GGTCCACACATGGGGCATAGCCATGGTCTCTCGGCTCCGCTTAACCACACGGGTCCAGTGTGTGC T C SNORA10,RPS2 Ensembl:ENSG00000206811,Ensembl:ENSG00000140988 snoRNA,Protein coding exon,intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr16:1962437..1962734 26863410 MeRIP-seq:(Medium) rs1555482948 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_760052,Human_RBP_ID_815726,Human_RBP_ID_894975,Human_RBP_ID_1513613,Human_RBP_ID_2470002,Human_RBP_ID_5097613,Human_RBP_ID_5288528,Human_RBP_ID_8251967,Human_RBP_ID_8429005,Human_RBP_ID_8805337,Human_RBP_ID_17126213,Human_RBP_ID_17669778,Human_RBP_ID_17884576,Human_RBP_ID_18530352,Human_RBP_ID_18674422,Human_RBP_ID_18941059,Human_RBP_ID_21959991,Human_RBP_ID_22705765,Human_RBP_ID_23114163,Human_RBP_ID_23118721,Human_RBP_ID_23127923,Human_RBP_ID_24559032,Human_RBP_ID_26575748,Human_RBP_ID_27796872 RMVar_hsa_circ_84382,RMVar_hsa_circ_116614,RMVar_hsa_circ_106418,RMVar_hsa_circ_96212,RMVar_hsa_circ_100569,RMVar_hsa_circ_95316,RMVar_hsa_circ_175587,RMVar_hsa_circ_175589,RMVar_hsa_circ_175591,RMVar_hsa_circ_81440,RMVar_hsa_circ_175590,RMVar_hsa_circ_175588,RMVar_hsa_circ_175585,RMVar_hsa_circ_175586 113093 RMVar_ID_113093 Human_SNP_ID_827042786 m1A Human chr16 + 30664871 30664871 30664871 GCACCAGCACACCCACCAGCACACCCACCAGCACTTCACCCCTTATCCCCCGGGCCTGCTGCCAC GCACCAGCACACCCACCAGCACACCCACCAGCCCTTCACCCCTTATCCCCCGGGCCTGCTGCCAC A C FBRS Ensembl:ENSG00000156860 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30664761..30665362 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_45045,Human_RBP_ID_5128603,Human_RBP_ID_5495531,Human_RBP_ID_17253958,Human_RBP_ID_17369520,Human_RBP_ID_22421628,Human_RBP_ID_27441629,Human_RBP_ID_27837831 Human_Splice_Rec_1703563,Human_Splice_Rec_1703617 Human_miRNA_ID_271942,Human_miRNA_ID_2052289,Human_miRNA_ID_2316559,Human_miRNA_ID_2319715,Human_miRNA_ID_2322872,Human_miRNA_ID_2326044,Human_miRNA_ID_2329143,Human_miRNA_ID_2520422,Human_miRNA_ID_2523584,Human_miRNA_ID_2653507,Human_miRNA_ID_2754705,Human_miRNA_ID_2775408,Human_miRNA_ID_2822772,Human_miRNA_ID_2828907,Human_miRNA_ID_2832066,Human_miRNA_ID_2836185,Human_miRNA_ID_2841540 RMVar_hsa_circ_5600,RMVar_hsa_circ_92132,RMVar_hsa_circ_123272,RMVar_hsa_circ_177916,RMVar_hsa_circ_85133,RMVar_hsa_circ_177917,RMVar_hsa_circ_177915,RMVar_hsa_circ_338639,RMVar_hsa_circ_11729,RMVar_hsa_circ_177918 113094 RMVar_ID_113094 Human_SNP_ID_827054437 m1A Human chr16 + 803728 803728 803728 GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGACCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG GGCTGTCCTAGGGGGACCCTGTGGCCTGCAGGCCCCAAGCAGCCCGGGGGTGGTGGGTGAATGTG A C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11248950 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113095 RMVar_ID_113095 Human_SNP_ID_827075630 m1A Human chr16 + 88518357 88518357 88518357 GTGGATGGATGAGTGGGTGGGTGGATAGATGGATGGATGAATGAATGGGTAGGTGGCTGACAGGG GTGGATGGATGAGTGGGTGGGTGGATAGATGGGTGGATGAATGAATGGGTAGGTGGCTGACAGGG A G ZFPM1 Ensembl:ENSG00000179588 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:88518349..88519052;chr16:88518351..88518994 26863196 MeRIP-seq:(Medium) rs1334619617 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 113096 RMVar_ID_113096 Human_SNP_ID_827098081 m1A Human chr16 + 67115033 67115032 67115034 GGTTAGTTGAACCAGGGATGAGCAGAAGAAACATAGCCTATTGGAGAGACTTGGAAAAGTTAGAG GGTTAGTTGAACCAGGGATGAGCAGAAGAAAC__AGCCTATTGGAGAGACTTGGAAAAGTTAGAG CAT C C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:67115021..67115104 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 LICA 1 - RMVar_hsa_circ_179025,RMVar_hsa_circ_90176 113097 RMVar_ID_113097 Human_SNP_ID_827103944 m1A Human chr16 + 662767 662767 662767 TCGATGACAGCGTGGACATGGGCGTCGTGGGCACCACGGCGGGCACGCTGTGGTTTGTCAGCTGG TCGATGACAGCGTGGACATGGGCGTCGTGGGCTCCACGGCGGGCACGCTGTGGTTTGTCAGCTGG A T WDR90 Ensembl:ENSG00000161996 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:662726..662911 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_891027,Human_RBP_ID_18982809,Human_RBP_ID_22944931 Human_Splice_Rec_1654822,Human_Splice_Rec_1654823,Human_Splice_Rec_1654964,Human_Splice_Rec_1654965,Human_Splice_Rec_1655026,Human_Splice_Rec_1655056,Human_Splice_Rec_1655138,Human_Splice_Rec_1655158,Human_Splice_Rec_1655159,Human_Splice_Rec_1655182,Human_Splice_Rec_1655183 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 113098 RMVar_ID_113098 Human_SNP_ID_827128674 m1A Human chr16 + 28591700 28591700 28591700 AGATACGTGGTGGCTTGTAAGGAACCCAAGAAAAAGTGATGCCGCCTGGCAGACTCGCCATCCCC AGATACGTGGTGGCTTGTAAGGAACCCAAGAACAAGTGATGCCGCCTGGCAGACTCGCCATCCCC A C SGF29 Ensembl:ENSG00000176476 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28591650..28591723 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113099 RMVar_ID_113099 Human_SNP_ID_827130870 m1A Human chr16 + 23558151 23558151 23558151 CGCAGCCCAGGCCTCGGTCAGCAACGGCGAAGACGCGGGCGGCGGCGCGGGCAGGGAGCTGGTGG CGCAGCCCAGGCCTCGGTCAGCAACGGCGAAGGCGCGGGCGGCGGCGCGGGCAGGGAGCTGGTGG A G UBFD1 Ensembl:ENSG00000103353 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:23558101..23558150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_761024,Human_RBP_ID_4357177,Human_RBP_ID_6501572,Human_RBP_ID_27811712 RMVar_hsa_circ_99560,RMVar_hsa_circ_177321 113100 RMVar_ID_113100 Human_SNP_ID_827131994 m1A Human chr16 + 28951182 28951182 28951182 TCTGTGGACTTGGTCACCGACAGCGATGAGGAAATTCTGGAGGTCGCCACCGCTCGCGGTGCCGC TCTGTGGACTTGGTCACCGACAGCGATGAGGACATTCTGGAGGTCGCCACCGCTCGCGGTGCCGC A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:28951001..28951203 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1841030,Human_RBP_ID_4361205,Human_RBP_ID_22944431,Human_RBP_ID_26328854 Human_miRNA_ID_2999462 RMVar_hsa_circ_81983,RMVar_hsa_circ_177691 113101 RMVar_ID_113101 Human_SNP_ID_827146781 m1A Human chr16 - 87708403 87708403 87708403 GGAAGAGGACAGTGAGGAGGTTGAGGGCGCCGAGGGTGGGGTCGACGACGAAGACAGCGGAGAGG GGAAGAGGACAGTGAGGAGGTTGAGGGCGCCGCGGGTGGGGTCGACGACGAAGACAGCGGAGAGG T G KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:87708278..87708421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_233555,Human_RBP_ID_818102,Human_RBP_ID_892743,Human_RBP_ID_3949651,Human_RBP_ID_5114000,Human_RBP_ID_9373311,Human_RBP_ID_18469811,Human_RBP_ID_18987095,Human_RBP_ID_20169188,Human_RBP_ID_22583096,Human_RBP_ID_22944709,Human_RBP_ID_23118501,Human_RBP_ID_24544550,Human_RBP_ID_26329307,Human_RBP_ID_26780738 Human_Splice_Rec_1748370,Human_Splice_Rec_1748371,Human_Splice_Rec_1748381,Human_Splice_Rec_1748396,Human_Splice_Rec_1748397,Human_Splice_Rec_1748414,Human_Splice_Rec_1748415,Human_Splice_Rec_1748434,Human_Splice_Rec_1748435,Human_Splice_Rec_1748456,Human_Splice_Rec_1748457,Human_Splice_Rec_1748470,Human_Splice_Rec_1748471,Human_Splice_Rec_1748475,Human_Splice_Rec_1748494,Human_Splice_Rec_1748495,Human_Splice_Rec_1748514,Human_Splice_Rec_1748515 RMVar_hsa_circ_95917,RMVar_hsa_circ_300861,RMVar_hsa_circ_63705,RMVar_hsa_circ_65390,RMVar_hsa_circ_15052,RMVar_hsa_circ_180431 113102 RMVar_ID_113102 Human_SNP_ID_827157957 m1A Human chr16 - 67658197 67658197 67658197 AGCCCCTGCCACCCTGACCCCCAGGTCCCCACACGCCAGCCGTACCCCCAGCTCCCCACTCCAGA AGCCCCTGCCACCCTGACCCCCAGGTCCCCACCCGCCAGCCGTACCCCCAGCTCCCCACTCCAGA T G ACD Ensembl:ENSG00000102977 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:67658085..67658284 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_234666,Human_RBP_ID_17077559,Human_RBP_ID_17257177,Human_RBP_ID_17371504,Human_RBP_ID_18939255 Human_miRNA_ID_1418466 113103 RMVar_ID_113103 Human_SNP_ID_827163748 m1A Human chr16 - 794325 794325 794325 CCTCAGAGACTTCCTGGCACCCCATTTCCCGAACCTGCCTCTCTCAGCACCCCCAAAGCGCCTCC CCTCAGAGACTTCCTGGCACCCCATTTCCCGACCCTGCCTCTCTCAGCACCCCCAAAGCGCCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:794323..794548 26863196 MeRIP-seq:(Medium) rs1203662847 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113104 RMVar_ID_113104 Human_SNP_ID_827163893 m1A Human chr16 + 2148732 2148732 2148732 CCGGGTCGGGCTCGGCGGGCGCGGGGTGCGGGACGGCCCAGGGCACGGCGGCTGCAGCGGGAGCA CCGGGTCGGGCTCGGCGGGCGCGGGGTGCGGGGCGGCCCAGGGCACGGCGGCTGCAGCGGGAGCA A G RAB26 Ensembl:ENSG00000167964 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2148685..2148829 26863196 MeRIP-seq:(Medium) rs907275969 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113105 RMVar_ID_113105 Human_SNP_ID_827164504 m1A Human chr16 - 11556719 11556719 11556719 TCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCAGGACCTTACCAGGCGGCCACTGGGCCTTCCTC TCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCTGGACCTTACCAGGCGGCCACTGGGCCTTCCTC T A LITAF Ensembl:ENSG00000189067 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:11556567..11556750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_4350003,Human_RBP_ID_22441785,Human_RBP_ID_24544681 Human_Splice_Rec_1678062,Human_Splice_Rec_1678068,Human_Splice_Rec_1678074,Human_Splice_Rec_1678082,Human_Splice_Rec_1678090,Human_Splice_Rec_1678096,Human_Splice_Rec_1678104,Human_Splice_Rec_1678116,Human_Splice_Rec_1678124,Human_Splice_Rec_1678130,Human_Splice_Rec_1678138,Human_Splice_Rec_1678144,Human_Splice_Rec_1678150,Human_Splice_Rec_1678156,Human_Splice_Rec_1678160,Human_Splice_Rec_1678166,Human_Splice_Rec_1678170,Human_Splice_Rec_1678176 RMVar_hsa_circ_24454,RMVar_hsa_circ_176273,RMVar_hsa_circ_274549,RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 113106 RMVar_ID_113106 Human_SNP_ID_827168100 m1A Human chr16 - 580974 580974 580974 ACCCAGGGCCAGCTGCCCAATACGCAGCACTTACCCGCCAGCCTGTAGGGCCGGCAGAGCCGAAG ACCCAGGGCCAGCTGCCCAATACGCAGCACTTGCCCGCCAGCCTGTAGGGCCGGCAGAGCCGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:580453..581326 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 113107 RMVar_ID_113107 Human_SNP_ID_827177989 m1A Human chr16 + 75636017 75636017 75636017 ATGATGCTCAGCTCACCCTTCTTGGTTTTACCAGGATTCCCCTGAACTCCAATTATGTCTCCCCG ATGATGCTCAGCTCACCCTTCTTGGTTTTACCTGGATTCCCCTGAACTCCAATTATGTCTCCCCG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:75635676..75636550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 113108 RMVar_ID_113108 Human_SNP_ID_827180423 m1A Human chr16 + 83808113 83808113 83808113 CCGAGACTGACCCCAAGACCGTGCAGGACCTCACCTCGGTGGTAAGGGACGGCTGTGAGGGCCGG CCGAGACTGACCCCAAGACCGTGCAGGACCTCGCCTCGGTGGTAAGGGACGGCTGTGAGGGCCGG A G HSBP1 Ensembl:ENSG00000230989 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:83808041..83808142 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_480393,Human_RBP_ID_817722,Human_RBP_ID_894802,Human_RBP_ID_1523396,Human_RBP_ID_4394023,Human_RBP_ID_5141969,Human_RBP_ID_5316716,Human_RBP_ID_9326106,Human_RBP_ID_12827312,Human_RBP_ID_19075263,Human_RBP_ID_22441136,Human_RBP_ID_23209714,Human_RBP_ID_23702680,Human_RBP_ID_27446036 Human_Splice_Rec_1745105,Human_Splice_Rec_1745109 Human_miRNA_ID_2007530 RMVar_hsa_circ_180248,RMVar_hsa_circ_101469 113109 RMVar_ID_113109 Human_SNP_ID_827182777 m1A Human chr16 + 670485 670485 670485 CAGTGTTCGGCCAAGAACCTGAGGAACATCTCAGAGCTGTTCTACTACGCCCAGAAGGCCGTCCT CAGTGTTCGGCCAAGAACCTGAGGAACATCTCCGAGCTGTTCTACTACGCCCAGAAGGCCGTCCT A C RHOT2 Ensembl:ENSG00000140983 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:670451..670550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_1846170,Human_RBP_ID_3946901,Human_RBP_ID_9372009,Human_RBP_ID_18683825,Human_RBP_ID_18982831,Human_RBP_ID_22802244,Human_RBP_ID_22946301,Human_RBP_ID_23114011,Human_RBP_ID_24558628,Human_RBP_ID_26328363,Human_RBP_ID_26948785,Human_RBP_ID_27811417 Human_Splice_Rec_1655250,Human_Splice_Rec_1655264,Human_Splice_Rec_1655265,Human_Splice_Rec_1655280,Human_Splice_Rec_1655281,Human_Splice_Rec_1655294,Human_Splice_Rec_1655302,Human_Splice_Rec_1655320,Human_Splice_Rec_1655321,Human_Splice_Rec_1655354,Human_Splice_Rec_1655355,Human_Splice_Rec_1655390,Human_Splice_Rec_1655391,Human_Splice_Rec_1655404,Human_Splice_Rec_1655405,Human_Splice_Rec_1655424,Human_Splice_Rec_1655425,Human_Splice_Rec_1655442,Human_Splice_Rec_1655443,Human_Splice_Rec_1655464,Human_Splice_Rec_1655465,Human_Splice_Rec_1655484,Human_Splice_Rec_1655485,Human_Splice_Rec_1655510,Human_Splice_Rec_1655524,Human_Splice_Rec_1655525,Human_Splice_Rec_1655546,Human_Splice_Rec_1655547,Human_Splice_Rec_1655560,Human_Splice_Rec_1655561,Human_Splice_Rec_1655570,Human_Splice_Rec_1655571,Human_Splice_Rec_1655584,Human_Splice_Rec_1655585,Human_Splice_Rec_1655599,Human_Splice_Rec_1655617 RMVar_hsa_circ_104960,RMVar_hsa_circ_119501,RMVar_hsa_circ_125130,RMVar_hsa_circ_175403,RMVar_hsa_circ_175405,RMVar_hsa_circ_76184,RMVar_hsa_circ_175406,RMVar_hsa_circ_175404 113110 RMVar_ID_113110 Human_SNP_ID_827184153 m1A Human chr16 + 84662446 84662446 84662446 ACTGTCCCCCTGAGAGTAGCTGGCACGTGGGTAACACAGAAATTTCTGTAGTGAAGCTTGGGCCT ACTGTCCCCCTGAGAGTAGCTGGCACGTGGGTTACACAGAAATTTCTGTAGTGAAGCTTGGGCCT A T KLHL36 Ensembl:ENSG00000135686 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17755862 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_9506,GWAS_ID_9507 113111 RMVar_ID_113111 Human_SNP_ID_827190572 m1A Human chr16 + 88726426 88726426 88726426 GATGATGCCAGCCTCCTCCACAGGCAGCAGGCAGTCCTGGTCTCTGTCCATCATCTCCTTGGCTG GATGATGCCAGCCTCCTCCACAGGCAGCAGGCTGTCCTGGTCTCTGTCCATCATCTCCTTGGCTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:88726376..88726475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113112 RMVar_ID_113112 Human_SNP_ID_827194052 m1A Human chr16 - 3731877 3731877 3731877 AGAAGAAGAACAACAAGAAAACCAACAAGAACAAAAGCAGCATCAGCCGCGCCAACAAGAAGAAG AGAAGAAGAACAACAAGAAAACCAACAAGAACGAAAGCAGCATCAGCCGCGCCAACAAGAAGAAG T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3731748..3731951 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue angioimmunoblastic_T_cell_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_45939,Human_RBP_ID_9372154,Human_RBP_ID_24544370,Human_RBP_ID_26328575 Human_Splice_Rec_1670782,Human_Splice_Rec_1670840,Human_Splice_Rec_1670850,Human_Splice_Rec_1670858 RMVar_hsa_circ_34329,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959 113113 RMVar_ID_113113 Human_SNP_ID_827214854 m1A Human chr16 + 30011970 30011970 30011970 TAGTTCCCCATGGGCTGCCATTTCTCACCCAAACCTTGCCACCCCCAAGCCGCCCCCCTGCCCGG TAGTTCCCCATGGGCTGCCATTTCTCACCCAAGCCTTGCCACCCCCAAGCCGCCCCCCTGCCCGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30011921..30012336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113114 RMVar_ID_113114 Human_SNP_ID_827214876 m1A Human chr16 + 30011970 30011970 30011970 TAGTTCCCCATGGGCTGCCATTTCTCACCCAAACCTTGCCACCCCCAAGCCGCCCCCCTGCCCGG TAGTTCCCCATGGGCTGCCATTTCTCACCCAACCCTTGCCACCCCCAAGCCGCCCCCCTGCCCGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30011921..30012336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113115 RMVar_ID_113115 Human_SNP_ID_827221923 m1A Human chr16 - 72787739 72787737 72787740 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGG___TGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC ACTG A ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs1429156408 Functional Loss DEL ICGC 32..34 33 STAD 1 - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 113116 RMVar_ID_113116 Human_SNP_ID_827248832 m1A Human chr16 - 46730095 46730095 46730095 GTGCAGGATGGCCTCAGTGGTGTGGGGTGAGGAGATGTTCCCTGGGGTGCAGGATGGCCTGGGTG GTGCAGGATGGCCTCAGTGGTGTGGGGTGAGGGGATGTTCCCTGGGGTGCAGGATGGCCTGGGTG T C MYLK3 Ensembl:ENSG00000140795 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:46730093..46730567 26863196 MeRIP-seq:(Medium) rs1017332144 Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_37357,RMVar_hsa_circ_44432 113117 RMVar_ID_113117 Human_SNP_ID_827249277 m1A Human chr16 - 28176038 28176021 28176038 GGGTCCCATCTCAGGATAAGATGGAAATCCGTAGCTGTCTGCCCAAACTCCTTTTGGCTCACCAT GGGTCCCATCTCAGGATAAGATGGAAATCCGT_________________CCTTTTGGCTCACCAT GAGTTTGGGCAGACAGCT G XPO6 Ensembl:ENSG00000169180 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:28176026..28176100 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..49 33 LIHC 1 - Human_RBP_ID_1840887,Human_RBP_ID_4360312,Human_RBP_ID_8806594,Human_RBP_ID_12710577,Human_RBP_ID_17485945 Human_Splice_Rec_1695024,Human_Splice_Rec_1695074,Human_Splice_Rec_1695222,Human_Splice_Rec_1695228 RMVar_hsa_circ_108269,RMVar_hsa_circ_177562,RMVar_hsa_circ_110257,RMVar_hsa_circ_177576,RMVar_hsa_circ_113397,RMVar_hsa_circ_177594,RMVar_hsa_circ_375742,RMVar_hsa_circ_177595,RMVar_hsa_circ_378642,RMVar_hsa_circ_123592,RMVar_hsa_circ_177606,RMVar_hsa_circ_368045,RMVar_hsa_circ_21087,RMVar_hsa_circ_41721,RMVar_hsa_circ_313081,RMVar_hsa_circ_34425,RMVar_hsa_circ_90873,RMVar_hsa_circ_177615,RMVar_hsa_circ_177612,RMVar_hsa_circ_272235,RMVar_hsa_circ_285097,RMVar_hsa_circ_285248,RMVar_hsa_circ_177616,RMVar_hsa_circ_177614,RMVar_hsa_circ_336098,RMVar_hsa_circ_353570,RMVar_hsa_circ_292998,RMVar_hsa_circ_177617,RMVar_hsa_circ_79990,RMVar_hsa_circ_294622,RMVar_hsa_circ_177619,RMVar_hsa_circ_177620 113118 RMVar_ID_113118 Human_SNP_ID_827262341 m1A Human chr16 + 1787758 1787733 1787758 CCTGGTGGTGGACACGCCCCCGGGGACCTCCGATGAGCACATGGCCACCATAGAAGCCCTGCGTC CCTGGTGG_________________________TGAGCACATGGCCACCATAGAAGCCCTGCGTC GTGGACACGCCCCCGGGGACCTCCGA G NUBP2 Ensembl:ENSG00000095906 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr16:1787624..1787839;chr16:1787624..1788200 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 9..33 33 BLCA 1 - Human_RBP_ID_233274,Human_RBP_ID_760709,Human_RBP_ID_5141788,Human_RBP_ID_9373623,Human_RBP_ID_18985090,Human_RBP_ID_22441210 Human_Splice_Rec_1660632,Human_Splice_Rec_1660633,Human_Splice_Rec_1660641,Human_Splice_Rec_1660656,Human_Splice_Rec_1660657,Human_Splice_Rec_1660668,Human_Splice_Rec_1660676,Human_Splice_Rec_1660677,Human_Splice_Rec_1660690,Human_Splice_Rec_1660691,Human_Splice_Rec_1660696,Human_Splice_Rec_1660697,Human_Splice_Rec_1660706,Human_Splice_Rec_1660707,Human_Splice_Rec_1660718,Human_Splice_Rec_1660719,Human_Splice_Rec_1660728,Human_Splice_Rec_1660734,Human_Splice_Rec_1660735,Human_Splice_Rec_1660742,Human_Splice_Rec_1660743 RMVar_hsa_circ_117286,RMVar_hsa_circ_115341,RMVar_hsa_circ_175557,RMVar_hsa_circ_175558 113119 RMVar_ID_113119 Human_SNP_ID_827264014 m1A Human chr16 + 12568729 12568729 12568729 TGGCCCCTCACCTCAGCGTGACAACCACGTCCACCTGGTGATCCTGAGAGCACACGATTCCCAAC TGGCCCCTCACCTCAGCGTGACAACCACGTCCCCCTGGTGATCCTGAGAGCACACGATTCCCAAC A C SNX29 Ensembl:ENSG00000048471 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:12568679..12568744 26863196 MeRIP-seq:(Medium) rs1075844 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_8917,GWAS_ID_8918,GWAS_ID_8919,GWAS_ID_8920 RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_88873,RMVar_hsa_circ_176383,RMVar_hsa_circ_176387,RMVar_hsa_circ_95036,RMVar_hsa_circ_176389,RMVar_hsa_circ_113689 113120 RMVar_ID_113120 Human_SNP_ID_827266007 m1A Human chr16 + 89581045 89581045 89581045 CATCCCGTCACCCGTCACACGGAACATCCCGTAACCCATCACATGGAACATCCCGTCACCTGTCA CATCCCGTCACCCGTCACACGGAACATCCCGTCACCCATCACATGGAACATCCCGTCACCTGTCA A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89581015..89581432 26863196 MeRIP-seq:(Medium) rs1352083744 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_199004,Human_RBP_ID_261183,Human_RBP_ID_2490840,Human_RBP_ID_9420297,Human_RBP_ID_22370132,Human_RBP_ID_24531483,Human_RBP_ID_26810792 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 113121 RMVar_ID_113121 Human_SNP_ID_827267609 m1A Human chr16 - 75648554 75648554 75648554 GATATCCGCGAGGCCCCGCGCTCAGCCTCCTCACCCCCGCTATCCGCGGCCTCCGGGTCCTCCTC GATATCCGCGAGGCCCCGCGCTCAGCCTCCTCGCCCCCGCTATCCGCGGCCTCCGGGTCCTCCTC T C KARS1 Ensembl:ENSG00000065427 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:75648526..75648575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_Splice_Rec_1741405 113122 RMVar_ID_113122 Human_SNP_ID_827269453 m1A Human chr16 - 87460131 87460131 87460131 AAAATAAGATGATTCTGTTTCTGTTCCCTCAGATCACTCCAAGAACTGAGGCCCCTGTCAGCAGT AAAATAAGATGATTCTGTTTCTGTTCCCTCAGGTCACTCCAAGAACTGAGGCCCCTGTCAGCAGT T C ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87460112..87460184 26863196 MeRIP-seq:(Medium) rs11648852 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,LAML,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_892740,Human_RBP_ID_4388177,Human_RBP_ID_18288196,Human_RBP_ID_18686177,Human_RBP_ID_25235365 Human_Splice_Rec_1748208,Human_Splice_Rec_1748232,Human_Splice_Rec_1748256 Human_miRNA_ID_2615960 GWAS_ID_9512,GWAS_ID_9513,GWAS_ID_9514,GWAS_ID_9515,GWAS_ID_9516,GWAS_ID_9517 RMVar_hsa_circ_80504,RMVar_hsa_circ_180417,RMVar_hsa_circ_122649,RMVar_hsa_circ_180422,RMVar_hsa_circ_316239,RMVar_hsa_circ_180418,RMVar_hsa_circ_180427,RMVar_hsa_circ_180424,RMVar_hsa_circ_75879,RMVar_hsa_circ_180425,RMVar_hsa_circ_361034,RMVar_hsa_circ_328542,RMVar_hsa_circ_180426 113123 RMVar_ID_113123 Human_SNP_ID_827269465 m1A Human chr16 - 87460131 87460131 87460131 AAAATAAGATGATTCTGTTTCTGTTCCCTCAGATCACTCCAAGAACTGAGGCCCCTGTCAGCAGT AAAATAAGATGATTCTGTTTCTGTTCCCTCAGCTCACTCCAAGAACTGAGGCCCCTGTCAGCAGT T G ZCCHC14 Ensembl:ENSG00000140948 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87460112..87460184 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_892740,Human_RBP_ID_4388177,Human_RBP_ID_18288196,Human_RBP_ID_18686177,Human_RBP_ID_25235365 Human_Splice_Rec_1748208,Human_Splice_Rec_1748232,Human_Splice_Rec_1748256 Human_miRNA_ID_2615960 RMVar_hsa_circ_80504,RMVar_hsa_circ_180417,RMVar_hsa_circ_122649,RMVar_hsa_circ_180422,RMVar_hsa_circ_316239,RMVar_hsa_circ_180418,RMVar_hsa_circ_180427,RMVar_hsa_circ_180424,RMVar_hsa_circ_75879,RMVar_hsa_circ_180425,RMVar_hsa_circ_361034,RMVar_hsa_circ_328542,RMVar_hsa_circ_180426 113124 RMVar_ID_113124 Human_SNP_ID_827272044 m1A Human chr16 + 18838125 18838125 18838125 GCCTGCTGGCCACCTCCACCATAGACAGCACCAGCAAACCCAGCCTCGCCTCCTGCTGTCCAGTC GCCTGCTGGCCACCTCCACCATAGACAGCACCGGCAAACCCAGCCTCGCCTCCTGCTGTCCAGTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr16:18838075..18838184;chr16:18838076..18838150 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 113125 RMVar_ID_113125 Human_SNP_ID_827272111 m1A Human chr16 - 56682522 56682522 56682522 CAGTTGGGGTCCATTTCGAGGCAAGGAGAAGCAGGAGTTCCCGATCAAGAGGAAAACACGCAGCG CAGTTGGGGTCCATTTCGAGGCAAGGAGAAGCTGGAGTTCCCGATCAAGAGGAAAACACGCAGCG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:56682472..56682670 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 113126 RMVar_ID_113126 Human_SNP_ID_827272668 m1A Human chr16 - 30096172 30096172 30096172 TCCAGGCGCCTGCGAACCCGGGCCCGGGGGGGACGGCGCCCGCCAGGAGCGCCCCCCACTCCCAG TCCAGGCGCCTGCGAACCCGGGCCCGGGGGGGGCGGCGCCCGCCAGGAGCGCCCCCCACTCCCAG T C YPEL3 Ensembl:ENSG00000090238 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30096050..30096193 26863196 MeRIP-seq:(Medium) rs1019074249 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4393000,Human_RBP_ID_5114212,Human_RBP_ID_5142214 Human_Splice_Rec_1701887,Human_Splice_Rec_1701901,Human_Splice_Rec_1701907,Human_Splice_Rec_1701939,Human_Splice_Rec_1701953 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_109141,RMVar_hsa_circ_177844 113127 RMVar_ID_113127 Human_SNP_ID_827272700 m1A Human chr16 + 66934345 66934345 66934345 GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGACCCCGCCGCCGCCTACCATCGCGGAACCACCA GGGGGTTGGCATTCTCCAGGAGGCCGCCGCCGCCCCCGCCGCCGCCTACCATCGCGGAACCACCA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:66934139..66934375 26863196 MeRIP-seq:(Medium) rs1427505058 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113128 RMVar_ID_113128 Human_SNP_ID_827292785 m1A Human chr16 - 2976993 2976993 2976993 CTGCACTGGCCATGCCCATGCCCACGGAGGGCACCCCGCCACCTCTGAGTGGCACCCCCATCCCA CTGCACTGGCCATGCCCATGCCCACGGAGGGCCCCCCGCCACCTCTGAGTGGCACCCCCATCCCA T G PKMYT1 Ensembl:ENSG00000127564 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:2976683..2977265 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3947207,Human_RBP_ID_4392790 Human_Splice_Rec_1667814,Human_Splice_Rec_1667834,Human_Splice_Rec_1667854,Human_Splice_Rec_1667880,Human_Splice_Rec_1667912,Human_Splice_Rec_1667926,Human_Splice_Rec_1667942,Human_Splice_Rec_1667948,Human_Splice_Rec_1667956,Human_Splice_Rec_1667962,Human_Splice_Rec_1667968 113129 RMVar_ID_113129 Human_SNP_ID_827298862 m1A Human chr16 + 1822265 1822265 1822265 GTCCCTAAACCCACCGGGGCGAGAAGTGAGCCAGGTCCCACACCCCCAGGTGAGACGCGGCACTT GTCCCTAAACCCACCGGGGCGAGAAGTGAGCCGGGTCCCACACCCCCAGGTGAGACGCGGCACTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1822261..1822399 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 113130 RMVar_ID_113130 Human_SNP_ID_827302512 m1A Human chr16 + 70158560 70158557 70158560 ACCACTCCTAGTGATTACTGACTTTAGTGCCTAAACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA ACCACTCCTAGTGATTACTGACTTTAGTGC___AACCTTTTTGGAAGGTTCTGGTTGGCTTGTTA CCTA C PDPR Ensembl:ENSG00000090857 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 31..33 33 SKCA 2 - Human_RBP_ID_18287002 Human_miRNA_ID_736151 RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 113131 RMVar_ID_113131 Human_SNP_ID_827307521 m1A Human chr16 + 4848208 4848208 4848208 GACGTCTGCGGCCCGCGTCGGCGCTGGGGACAAAGGTGCGTGTCGTTGTCGGGTCCGGGCTCTCT GACGTCTGCGGCCCGCGTCGGCGCTGGGGACAGAGGTGCGTGTCGTTGTCGGGTCCGGGCTCTCT A G UBN1 Ensembl:ENSG00000118900 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr16:4847783..4848230;chr16:4847507..4848256 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_Splice_Rec_1673947 RMVar_hsa_circ_76543,RMVar_hsa_circ_176075 113132 RMVar_ID_113132 Human_SNP_ID_827319901 m1A Human chr16 - 74304396 74304396 74304396 AGTGAATGATTTTGATGCTGTACTAGGGTCTCACCGTAACAAGTGTTCAACTCCAACTTCCTCAG AGTGAATGATTTTGATGCTGTACTAGGGTCTCGCCGTAACAAGTGTTCAACTCCAACTTCCTCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74304363..74304514 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 113133 RMVar_ID_113133 Human_SNP_ID_827320959 m1A Human chr16 + 681843 681843 681843 GCGAAACCACGAGGGTGATGAGGACGACAGCCACGTCCGGGCCCAGCAGGCCTGCATTGAGGCCA GCGAAACCACGAGGGTGATGAGGACGACAGCCTCGTCCGGGCCCAGCAGGCCTGCATTGAGGCCA A T STUB1 Ensembl:ENSG00000103266 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:681776..682035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 testis non_seminoma 5 testis Human_RBP_ID_1005479,Human_RBP_ID_4383163,Human_RBP_ID_26328379 Human_Splice_Rec_1655708,Human_Splice_Rec_1655709,Human_Splice_Rec_1655720,Human_Splice_Rec_1655721,Human_Splice_Rec_1655730,Human_Splice_Rec_1655740,Human_Splice_Rec_1655741,Human_Splice_Rec_1655750,Human_Splice_Rec_1655756,Human_Splice_Rec_1655757,Human_Splice_Rec_1655766,Human_Splice_Rec_1655767,Human_Splice_Rec_1655774,Human_Splice_Rec_1655775,Human_Splice_Rec_1655780,Human_Splice_Rec_1655781 Human_miRNA_ID_1157614 113134 RMVar_ID_113134 Human_SNP_ID_827322948 m1A Human chr16 - 75647877 75647877 75647877 TTTGCCCAAATCCATCGCCTCCGCCATGTCTGACGCCGAGCACTACTAGAAGAGCTACCCCCTCG TTTGCCCAAATCCATCGCCTCCGCCATGTCTGCCGCCGAGCACTACTAGAAGAGCTACCCCCTCG T G KARS1 Ensembl:ENSG00000065427 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:75647826..75648033 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 113135 RMVar_ID_113135 Human_SNP_ID_827323060 m1A Human chr16 + 29805137 29805136 29805137 GTCCCGCCAGGTGGAGGACCTGGAACGCGTGGAGGGCATAACGGGGAAACAGATGGAGTCCTTCC GTCCCGCCAGGTGGAGGACCTGGAACGCGTGG_GGGCATAACGGGGAAACAGATGGAGTCCTTCC GA G KIF22 Ensembl:ENSG00000079616 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29804756..29805187 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_889614,Human_RBP_ID_5355750,Human_RBP_ID_9345801,Human_RBP_ID_18162097,Human_RBP_ID_18677166,Human_RBP_ID_18985966,Human_RBP_ID_19071287,Human_RBP_ID_22654074,Human_RBP_ID_22945023,Human_RBP_ID_23685997 Human_Splice_Rec_1699838,Human_Splice_Rec_1699839,Human_Splice_Rec_1699874,Human_Splice_Rec_1699875,Human_Splice_Rec_1699906,Human_Splice_Rec_1699907,Human_Splice_Rec_1699930,Human_Splice_Rec_1699931,Human_Splice_Rec_1699956,Human_Splice_Rec_1699957 RMVar_hsa_circ_97524,RMVar_hsa_circ_177750,RMVar_hsa_circ_101705,RMVar_hsa_circ_177755 113136 RMVar_ID_113136 Human_SNP_ID_827323800 m1A Human chr16 + 67868423 67868423 67868423 GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGAAGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC GCCATTGTGGAGAAGTTGTCTGTAAGTAGGGATGAAAGCCAGGGTGCAGGTGGCTCCTTTCCCAC A T NUTF2 Ensembl:ENSG00000102898 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:67868420..67868519 26863196 MeRIP-seq:(Medium) rs2271294 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_12779553,Human_RBP_ID_19074777,Human_RBP_ID_23696275 Human_Splice_Rec_1729562,Human_Splice_Rec_1729566,Human_Splice_Rec_1729574,Human_Splice_Rec_1729582,Human_Splice_Rec_1729590,Human_Splice_Rec_1729598,Human_Splice_Rec_1729606 GWAS_ID_12115,GWAS_ID_12116,GWAS_ID_12117,GWAS_ID_12118,GWAS_ID_12119,GWAS_ID_12120 RMVar_hsa_circ_84061,RMVar_hsa_circ_283198,RMVar_hsa_circ_179132,RMVar_hsa_circ_292199,RMVar_hsa_circ_179133 113137 RMVar_ID_113137 Human_SNP_ID_827325183 m1A Human chr16 + 721927 721927 721927 CCGGCTGTGCCGGCAGCGTCTGCTATCGCCGCAAGGATCTCTGGAAGGTAACCTGGGGATCCCTG CCGGCTGTGCCGGCAGCGTCTGCTATCGCCGCCAGGATCTCTGGAAGGTAACCTGGGGATCCCTG A C ANTKMT Ensembl:ENSG00000103254 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:721122..722207 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 7 ovary Human_RBP_ID_22944541 Human_Splice_Rec_1656079,Human_Splice_Rec_1656085,Human_Splice_Rec_1656095,Human_Splice_Rec_1656107 RMVar_hsa_circ_87973,RMVar_hsa_circ_175434 113138 RMVar_ID_113138 Human_SNP_ID_827326129 m1A Human chr16 + 89563073 89563073 89563073 AAAGCCCTCCTGGGGACTTGGAATCAGTCGGCAGTCATGCTGGGTCTCCACGTGGTGTGTTTCGT AAAGCCCTCCTGGGGACTTGGAATCAGTCGGCGGTCATGCTGGGTCTCCACGTGGTGTGTTTCGT A G RPL13 Ensembl:ENSG00000167526 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89563023..89563323 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_481958,Human_RBP_ID_1005953,Human_RBP_ID_1525861,Human_RBP_ID_1847997,Human_RBP_ID_2490751,Human_RBP_ID_3501766,Human_RBP_ID_5142381,Human_RBP_ID_6547564,Human_RBP_ID_8443010,Human_RBP_ID_8811299,Human_RBP_ID_9066528,Human_RBP_ID_12856722,Human_RBP_ID_17652822,Human_RBP_ID_17691045,Human_RBP_ID_17882904,Human_RBP_ID_18687641,Human_RBP_ID_22053653,Human_RBP_ID_22802680,Human_RBP_ID_23707561,Human_RBP_ID_27447500 Human_miRNA_ID_2442100 RMVar_hsa_circ_120915,RMVar_hsa_circ_180652 113139 RMVar_ID_113139 Human_SNP_ID_827331118 m1A Human chr16 + 29906761 29906759 29906762 AAAGTGAGCTGTGCCATGCAATGAAGGGACAGAGGAGGACCCACGACTTGGCCAGCAGAGCCGGG AAAGTGAGCTGTGCCATGCAATGAAGGGACA___GAGGACCCACGACTTGGCCAGCAGAGCCGGG AGAG A ASPHD1 Ensembl:ENSG00000174939 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29906539..29906803 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 STAD 1 - 113140 RMVar_ID_113140 Human_SNP_ID_827334387 m1A Human chr16 + 90027721 90027721 90027721 TGGGCTCGCTCCAGAGGACATGAGCAAGGAGCAGGTGAGCAGAGCGGGCTGTGGCCCAGTCCCCG TGGGCTCGCTCCAGAGGACATGAGCAAGGAGCGGGTGAGCAGAGCGGGCTGTGGCCCAGTCCCCG A G GAS8 Ensembl:ENSG00000141013 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr16:90027626..90027763;chr16:90027692..90027769 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - Human_RBP_ID_892989,Human_RBP_ID_12864616 Human_Splice_Rec_1755308,Human_Splice_Rec_1755309,Human_Splice_Rec_1755314,Human_Splice_Rec_1755315,Human_Splice_Rec_1755318,Human_Splice_Rec_1755319,Human_Splice_Rec_1755338,Human_Splice_Rec_1755339,Human_Splice_Rec_1755344,Human_Splice_Rec_1755345,Human_Splice_Rec_1755354,Human_Splice_Rec_1755355,Human_Splice_Rec_1755360,Human_Splice_Rec_1755361,Human_Splice_Rec_1755380,Human_Splice_Rec_1755381,Human_Splice_Rec_1755406,Human_Splice_Rec_1755408,Human_Splice_Rec_1755409,Human_Splice_Rec_1755428,Human_Splice_Rec_1755429,Human_Splice_Rec_1755436,Human_Splice_Rec_1755437 RMVar_hsa_circ_365495 113141 RMVar_ID_113141 Human_SNP_ID_827336881 m1A Human chr16 - 72959766 72959766 72959766 CGGTGAGGAGGGGGACGAGGAGAGTGACGTGGAGAACCTGGCCGGGGAGATCGTCTACCAGCCGG CGGTGAGGAGGGGGACGAGGAGAGTGACGTGGTGAACCTGGCCGGGGAGATCGTCTACCAGCCGG T A ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:72959716..72959848 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium clear_cell_carcinoma 3 uterus Human_RBP_ID_5524664 RMVar_hsa_circ_26118,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011,RMVar_hsa_circ_294312,RMVar_hsa_circ_91300,RMVar_hsa_circ_112909,RMVar_hsa_circ_97467,RMVar_hsa_circ_179900,RMVar_hsa_circ_179901,RMVar_hsa_circ_270069,RMVar_hsa_circ_100227,RMVar_hsa_circ_179903,RMVar_hsa_circ_179904,RMVar_hsa_circ_179902,RMVar_hsa_circ_288691,RMVar_hsa_circ_179906,RMVar_hsa_circ_179907 113142 RMVar_ID_113142 Human_SNP_ID_827351836 m1A Human chr16 + 57753234 57753234 57753234 CAACCCCAGCGCCCCCCTCCGGCGCATCTATGAGCGGCCCAGCACAACCTGCAGCAAGCCTCAGA CAACCCCAGCGCCCCCCTCCGGCGCATCTATGGGCGGCCCAGCACAACCTGCAGCAAGCCTCAGA A G KATNB1 Ensembl:ENSG00000140854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:57753186..57753301 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_Splice_Rec_1719557,Human_Splice_Rec_1719601 RMVar_hsa_circ_118902,RMVar_hsa_circ_178725,RMVar_hsa_circ_101399,RMVar_hsa_circ_76573,RMVar_hsa_circ_84019,RMVar_hsa_circ_178726,RMVar_hsa_circ_127044,RMVar_hsa_circ_178727,RMVar_hsa_circ_178728,RMVar_hsa_circ_178729,RMVar_hsa_circ_105504,RMVar_hsa_circ_178730 113143 RMVar_ID_113143 Human_SNP_ID_827354777 m1A Human chr16 - 61055932 61055932 61055932 TAAAGAGTTCTATAGATTGAGAAGCTATCTGCAGTGGAGCCGCCACCAAAATGCAGATTTTCGTG TAAAGAGTTCTATAGATTGAGAAGCTATCTGCCGTGGAGCCGCCACCAAAATGCAGATTTTCGTG T G RPS27AP16 Ensembl:ENSG00000224631 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112657530 Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_26811438 113144 RMVar_ID_113144 Human_SNP_ID_827354789 m1A Human chr16 - 61055932 61055932 61055932 TAAAGAGTTCTATAGATTGAGAAGCTATCTGCAGTGGAGCCGCCACCAAAATGCAGATTTTCGTG TAAAGAGTTCTATAGATTGAGAAGCTATCTGCGGTGGAGCCGCCACCAAAATGCAGATTTTCGTG T C RPS27AP16 Ensembl:ENSG00000224631 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs112657530 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_26811438 113145 RMVar_ID_113145 Human_SNP_ID_827367138 m1A Human chr16 + 4937110 4937110 4937110 GCGGGCCGGGCGCGCACCGAGGGGCGGGCGGGAGCGCAGGTGAGCGAGCGGCGGCGCGGGGAGCC GCGGGCCGGGCGCGCACCGAGGGGCGGGCGGGGGCGCAGGTGAGCGAGCGGCGGCGCGGGGAGCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:4936986..4937158 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113146 RMVar_ID_113146 Human_SNP_ID_827370246 m1A Human chr16 + 30769235 30769235 30769235 CTCAGAGATGGATGTGACAGGTCAGGCTTTTGAGGACATGCAGGAACAGAACGGGCGGCTGCTAC CTCAGAGATGGATGTGACAGGTCAGGCTTTTGGGGACATGCAGGAACAGAACGGGCGGCTGCTAC A G RNF40 Ensembl:ENSG00000103549 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:30769157..30769350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_1281819,Human_RBP_ID_1517048,Human_RBP_ID_1841643,Human_RBP_ID_6508528,Human_RBP_ID_8432500,Human_RBP_ID_8807256,Human_RBP_ID_9284806,Human_RBP_ID_9372703,Human_RBP_ID_12721397,Human_RBP_ID_17875694,Human_RBP_ID_22801277,Human_RBP_ID_26328925,Human_RBP_ID_26943606,Human_RBP_ID_27811795 Human_Splice_Rec_1704172,Human_Splice_Rec_1704224,Human_Splice_Rec_1704258,Human_Splice_Rec_1704302 RMVar_hsa_circ_60106,RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970 113147 RMVar_ID_113147 Human_SNP_ID_827385406 m1A Human chr16 - 1612415 1612415 1612415 GGACGCAGATACTGCCGCCACTCACCCTAGCGAAGCCGGCCCGCCGCCCTCAGCAGCAGTTCCGG GGACGCAGATACTGCCGCCACTCACCCTAGCGGAGCCGGCCCGCCGCCCTCAGCAGCAGTTCCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1612403..1612686 26863196 MeRIP-seq:(Medium) rs538504578 Functional Loss SNV ICGC 33..33 33 STAD 1 - 113148 RMVar_ID_113148 Human_SNP_ID_827387082 m1A Human chr16 - 88731933 88731933 88731933 AGTCCCTCCCCCCAGACTCAGTGCATCCCCACACCCCGCCCTCTCCCCTCCCCAGATCTGCTTCC AGTCCCTCCCCCCAGACTCAGTGCATCCCCACGCCCCGCCCTCTCCCCTCCCCAGATCTGCTTCC T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:88731672..88731957 26863196 MeRIP-seq:(Medium) rs76070043 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,COCA,central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 5 prostate,brain Human_RBP_ID_5128270,Human_RBP_ID_17077723,Human_RBP_ID_18939690,Human_RBP_ID_26779829,Human_RBP_ID_27837952 RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_105733,RMVar_hsa_circ_180534,RMVar_hsa_circ_180536,RMVar_hsa_circ_115425,RMVar_hsa_circ_180538,RMVar_hsa_circ_180539,RMVar_hsa_circ_116774,RMVar_hsa_circ_126889,RMVar_hsa_circ_180546,RMVar_hsa_circ_180547,RMVar_hsa_circ_111816,RMVar_hsa_circ_180548 113149 RMVar_ID_113149 Human_SNP_ID_827388076 m1A Human chr16 + 10547629 10547629 10547629 GAAAGCAAGAAGCACCAACATTTTCACAGGGCAGGGCGAGTCGAGGCGAGGGGTCACGTTTAAAG GAAAGCAAGAAGCACCAACATTTTCACAGGGCCGGGCGAGTCGAGGCGAGGGGTCACGTTTAAAG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:10547551..10580675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach 113150 RMVar_ID_113150 Human_SNP_ID_827400453 m1A Human chr16 + 69340264 69340264 69340264 ACAAGCTGGTGTCGCTGGGGACCTGCTTTGGAAAATTCACTAAAACCCACAAGTTTCGGTTGCAC ACAAGCTGGTGTCGCTGGGGACCTGCTTTGGATAATTCACTAAAACCCACAAGTTTCGGTTGCAC A T NIP7 Ensembl:ENSG00000132603 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:69340214..69340314 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1005201,Human_RBP_ID_1521179,Human_RBP_ID_17255079,Human_RBP_ID_17879887,Human_RBP_ID_22421714,Human_RBP_ID_22442131,Human_RBP_ID_22759869 Human_Splice_Rec_1732972,Human_Splice_Rec_1732973,Human_Splice_Rec_1732980,Human_Splice_Rec_1732984,Human_Splice_Rec_1732985,Human_Splice_Rec_1732992,Human_Splice_Rec_1732993,Human_Splice_Rec_1732997,Human_Splice_Rec_1733000,Human_Splice_Rec_1733001,Human_Splice_Rec_1733005 113151 RMVar_ID_113151 Human_SNP_ID_827403945 m1A Human chr16 - 68294716 68294716 68294716 GAAGGTCCGGTAGGTGGCCCTCCCGGGAGCCCACGAAGAACAACCTAGAAGGATGAGAAATGTGT GAAGGTCCGGTAGGTGGCCCTCCCGGGAGCCCTCGAAGAACAACCTAGAAGGATGAGAAATGTGT T A SLC7A6OS Ensembl:ENSG00000103061 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:68291623..68294840 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113152 RMVar_ID_113152 Human_SNP_ID_827404329 m1A Human chr16 + 23570949 23570947 23570950 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTT___AAAAAAAAAAAGCAGTTTCAATTGAAATATT TTAA T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 113153 RMVar_ID_113153 Human_SNP_ID_827404803 m1A Human chr16 + 55505702 55505702 55505702 CCACCAACCCTCAGAGCCACCCCTAAAGAGATACTTTGATATTTTCAACGCAGCCCTGCTTTGGG CCACCAACCCTCAGAGCCACCCCTAAAGAGATCCTTTGATATTTTCAACGCAGCCCTGCTTTGGG A C MMP2 Ensembl:ENSG00000087245 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7201 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_miRNA_ID_1646329,Human_miRNA_ID_1651855 Clinvar_Rec_544 GWAS_ID_12538,GWAS_ID_12539,GWAS_ID_12540,GWAS_ID_12541,GWAS_ID_12542,GWAS_ID_12543,GWAS_ID_12544 RMVar_hsa_circ_89298,RMVar_hsa_circ_178492 113154 RMVar_ID_113154 Human_SNP_ID_827414801 m1A Human chr16 - 30927803 30927803 30927803 GTGGCTCCTCTGTCAGCTTCCATCCGCTCCCCAAGCTGGCGCCCTCCTCGCCGTTGTCGGCCCTA GTGGCTCCTCTGTCAGCTTCCATCCGCTCCCCGAGCTGGCGCCCTCCTCGCCGTTGTCGGCCCTA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:30927692..30927825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - 113155 RMVar_ID_113155 Human_SNP_ID_827422440 m1A Human chr16 - 89286135 89286135 89286135 GGTACGGAGGGAACCCGCAGCAGAGCAACAGGAAAGGCGAGACGCCGCTGAAAGTGGCCAACTCC GGTACGGAGGGAACCCGCAGCAGAGCAACAGGGAAGGCGAGACGCCGCTGAAAGTGGCCAACTCC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89286086..89286200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_45257,Human_RBP_ID_22654682,Human_RBP_ID_22944495 Human_Splice_Rec_1750732,Human_Splice_Rec_1750733,Human_Splice_Rec_1750756,Human_Splice_Rec_1750757,Human_Splice_Rec_1750798,Human_Splice_Rec_1750799,Human_Splice_Rec_1750822,Human_Splice_Rec_1750823,Human_Splice_Rec_1750850,Human_Splice_Rec_1750851,Human_Splice_Rec_1750855,Human_Splice_Rec_1750862,Human_Splice_Rec_1750863,Human_Splice_Rec_1750866,Human_Splice_Rec_1750867,Human_Splice_Rec_1750882,Human_Splice_Rec_1750883,Human_Splice_Rec_1750892 Human_miRNA_ID_1347441,Human_miRNA_ID_1810054 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_95669,RMVar_hsa_circ_269582,RMVar_hsa_circ_180608 113156 RMVar_ID_113156 Human_SNP_ID_827427517 m1A Human chr16 - 46971941 46971941 46971941 TTTTATCCATTTTCAAAGGCATACAGAAAGTTAGCCAAGGAATATCATCCTGATAAGAATCCAAA TTTTATCCATTTTCAAAGGCATACAGAAAGTTCGCCAAGGAATATCATCCTGATAAGAATCCAAA T G DNAJA2 Ensembl:ENSG00000069345 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:46971896..46971996 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 2 breast Human_RBP_ID_895416,Human_RBP_ID_1842767,Human_RBP_ID_4395290,Human_RBP_ID_9345825 Human_Splice_Rec_1708338,Human_Splice_Rec_1708339,Human_Splice_Rec_1708354,Human_Splice_Rec_1708355 RMVar_hsa_circ_4706,RMVar_hsa_circ_19704,RMVar_hsa_circ_57494 113157 RMVar_ID_113157 Human_SNP_ID_827431019 m1A Human chr16 - 4847199 4847199 4847199 TGTGGTGAGTCCGAGCGGCCGGGCCAACCGAGACGCGCCGGGGAGCTACCCGCCTGGGCGCGGGG TGTGGTGAGTCCGAGCGGCCGGGCCAACCGAGCCGCGCCGGGGAGCTACCCGCCTGGGCGCGGGG T G GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:4847192..4847274 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_889425,Human_RBP_ID_22052908,Human_RBP_ID_26780174 113158 RMVar_ID_113158 Human_SNP_ID_827433381 m1A Human chr16 - 89281917 89281917 89281917 GGAGAAATTCAAGGACGGTGCAGAGAAAGAAAAGGGCGACCCAGTGAAGATGAGCAACGGGAATG GGAGAAATTCAAGGACGGTGCAGAGAAAGAAAGGGGCGACCCAGTGAAGATGAGCAACGGGAATG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr16:89281614..89281950 26863196 MeRIP-seq:(Medium) rs1383324924 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_889106,Human_RBP_ID_6546044,Human_RBP_ID_8442248,Human_RBP_ID_12847851,Human_RBP_ID_22053612,Human_RBP_ID_26329406,Human_RBP_ID_27811333 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 113159 RMVar_ID_113159 Human_SNP_ID_827444760 m1A Human chr16 + 28836057 28836057 28836057 TCATGGGGGGCCCCCCCAAGGCGCGGTGCCCCAGAGTGGGGTGCCTGCACTCTCAGCTTCCACAC TCATGGGGGGCCCCCCCAAGGCGCGGTGCCCCCGAGTGGGGTGCCTGCACTCTCAGCTTCCACAC A C ATXN2L Ensembl:ENSG00000168488 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:28835622..28836144 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 7 head and neck Human_RBP_ID_46305,Human_RBP_ID_5128091,Human_RBP_ID_17078174,Human_RBP_ID_17371382,Human_RBP_ID_18189905,Human_RBP_ID_20111310,Human_RBP_ID_23209597,Human_RBP_ID_26941986 Human_Splice_Rec_1697677,Human_Splice_Rec_1697853,Human_Splice_Rec_1698079,Human_Splice_Rec_1698085 113160 RMVar_ID_113160 Human_SNP_ID_827451620 m1A Human chr16 + 66890101 66890101 66890101 CAGGAGTTTGAGACCAGCCTGACCAACATGGTAAAACTCCATCTCTACTAAAAATACAAAAATTA CAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATTA A G PDP2 Ensembl:ENSG00000172840 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_90756,RMVar_hsa_circ_178998 113161 RMVar_ID_113161 Human_SNP_ID_827455945 m1A Human chr16 + 30526428 30526428 30526428 CAACGCCTCCCGCTCCATCCCCGCGGGCTCCCAGTGCAGCGGCGGCGGCGATGGCGGCCGATCCC CAACGCCTCCCGCTCCATCCCCGCGGGCTCCCGGTGCAGCGGCGGCGGCGATGGCGGCCGATCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr16:30525795..30532345;chr16:30525707..30532345 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113162 RMVar_ID_113162 Human_SNP_ID_827472645 m1A Human chr16 - 31191501 31191501 31191501 CCTTGGGTGATCAGGAATTGGAAGGTTACAAAATAACGAGGGTAACACTGGGTACAGGACAAAAA CCTTGGGTGATCAGGAATTGGAAGGTTACAAATTAACGAGGGTAACACTGGGTACAGGACAAAAA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:31191451..31191500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney 113163 RMVar_ID_113163 Human_SNP_ID_827475633 m1A Human chr16 + 1964506 1964482 1964506 CGAGCTCCGCGGCCTCGGCCCCGGCCCCGTCCACGGCCGCGACCCCGGCCCCGGATGCCACTGCC CGAGCTCCG________________________CGGCCGCGACCCCGGCCCCGGATGCCACTGCC GCGGCCTCGGCCCCGGCCCCGTCCA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:1964323..1964825 26863196 MeRIP-seq:(Medium) rs762808124 Functional Loss DEL ICGC 10..33 33 KIRP 1 - 113164 RMVar_ID_113164 Human_SNP_ID_827484813 m1A Human chr16 + 10743880 10743880 10743880 CGGCAAAGGCGACGGAATGGAGGAGGTGCCTCACGGTAAGCTCGCGGAGGGGGCGTGGGTCGCGG CGGCAAAGGCGACGGAATGGAGGAGGTGCCTCGCGGTAAGCTCGCGGAGGGGGCGTGGGTCGCGG A G NUBP1 Ensembl:ENSG00000103274 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:10743826..10747234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_4394389,Human_RBP_ID_19070895 Human_Splice_Rec_1677047,Human_Splice_Rec_1677057,Human_Splice_Rec_1677075,Human_Splice_Rec_1677095,Human_Splice_Rec_1677107 113165 RMVar_ID_113165 Human_SNP_ID_827488183 m1A Human chr16 - 11556737 11556737 11556737 ATTTCTTATCTGGTATGTTCTGTTTCTGTTTTAGGTAAAATGTCGGTTCCAGGACCTTACCAGGC ATTTCTTATCTGGTATGTTCTGTTTCTGTTTTTGGTAAAATGTCGGTTCCAGGACCTTACCAGGC T A LITAF Ensembl:ENSG00000189067 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:11556674..11556775 26863410 MeRIP-seq:(Medium) rs761962106 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 12 kidney RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 113166 RMVar_ID_113166 Human_SNP_ID_827488920 m1A Human chr16 + 86509916 86509916 86509916 ACTTGCTCGCCAGGTTGGTGGAGGCGGGGCGGATTCTGCTGGCGGCCGCGGGGCGGCGAGAGTGG ACTTGCTCGCCAGGTTGGTGGAGGCGGGGCGGGTTCTGCTGGCGGCCGCGGGGCGGCGAGAGTGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86509531..86510296 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113167 RMVar_ID_113167 Human_SNP_ID_827497690 m1A Human chr16 - 28608540 28608540 28608540 GATCTACCAGGGTGGTGACCTGGAGAAGTGTCACCGAGCTCCCATCTTCATGCGGGTGCCCTTCC GATCTACCAGGGTGGTGACCTGGAGAAGTGTCTCCGAGCTCCCATCTTCATGCGGGTGCCCTTCC T A SULT1A1 Ensembl:ENSG00000196502 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:28608440..28608576 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_762803,Human_RBP_ID_22441883 Human_Splice_Rec_1697130,Human_Splice_Rec_1697131,Human_Splice_Rec_1697158,Human_Splice_Rec_1697159,Human_Splice_Rec_1697182,Human_Splice_Rec_1697183,Human_Splice_Rec_1697196,Human_Splice_Rec_1697197,Human_Splice_Rec_1697214,Human_Splice_Rec_1697215,Human_Splice_Rec_1697228,Human_Splice_Rec_1697229,Human_Splice_Rec_1697244,Human_Splice_Rec_1697245,Human_Splice_Rec_1697258,Human_Splice_Rec_1697259 RMVar_hsa_circ_290578,RMVar_hsa_circ_359534,RMVar_hsa_circ_333116 113168 RMVar_ID_113168 Human_SNP_ID_827498570 m1A Human chr16 + 1656988 1656988 1656988 CCTGAAGCTCATTTCCACCGAGGTCAACCCCAAGCTGGTGAGTGGGTTGGAGCCCAGCCCCTCTG CCTGAAGCTCATTTCCACCGAGGTCAACCCCACGCTGGTGAGTGGGTTGGAGCCCAGCCCCTCTG A C AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:1656950..1659994 26863196 MeRIP-seq:(Medium) rs753035998 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_22053774 Human_Splice_Rec_1659845,Human_Splice_Rec_1659883,Human_Splice_Rec_1659961 RMVar_hsa_circ_23574,RMVar_hsa_circ_175524,RMVar_hsa_circ_374387,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_32654,RMVar_hsa_circ_175530,RMVar_hsa_circ_93092 113169 RMVar_ID_113169 Human_SNP_ID_827499247 m1A Human chr16 + 56451153 56451153 56451153 TCTGCTGGATGTACTTGTTGCCGAACTGAGTGACCCCCCGGGGCCAGCCGGTCTGCGAGCGATTG TCTGCTGGATGTACTTGTTGCCGAACTGAGTGCCCCCCCGGGGCCAGCCGGTCTGCGAGCGATTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56451114..56451294 26863196 MeRIP-seq:(Medium) rs755431752 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 113170 RMVar_ID_113170 Human_SNP_ID_827503258 m1A Human chr16 - 29840380 29840380 29840380 GAGGGATGGCCTGGCGCTCCTCCACCACCTCCACTTTGGCAGATGGCACATACTCCAGGGGTCCG GAGGGATGGCCTGGCGCTCCTCCACCACCTCCGCTTTGGCAGATGGCACATACTCCAGGGGTCCG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:29840102..29841688 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 113171 RMVar_ID_113171 Human_SNP_ID_827503765 m1A Human chr16 - 74452154 74452154 74452154 CAGTGGGTCAGGAAGTGGGAGCCAGAGGTTTGACTCACTTTGCTTTATTTTTCAGGCTACAATAC CAGTGGGTCAGGAAGTGGGAGCCAGAGGTTTGTCTCACTTTGCTTTATTTTTCAGGCTACAATAC T A GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:74452104..74452214 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_233243,Human_RBP_ID_479445,Human_RBP_ID_6536466,Human_RBP_ID_8187164,Human_RBP_ID_9353128,Human_RBP_ID_26446356 Human_miRNA_ID_866941,Human_miRNA_ID_2383139,Human_miRNA_ID_2846640,Human_miRNA_ID_2849665 RMVar_hsa_circ_100317,RMVar_hsa_circ_121633,RMVar_hsa_circ_179934,RMVar_hsa_circ_179935 113172 RMVar_ID_113172 Human_SNP_ID_827508470 m1A Human chr16 + 28497555 28497555 28497555 GCTTTTGAGTCCAGGGAGGGAGGACCTTGGGGAGGGCGGGTAGAGGCCGAGGAATCTGCAGGCGC GCTTTTGAGTCCAGGGAGGGAGGACCTTGGGGGGGGCGGGTAGAGGCCGAGGAATCTGCAGGCGC A G APOBR Ensembl:ENSG00000184730 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28497270..28497902 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 113173 RMVar_ID_113173 Human_SNP_ID_827514046 m1A Human chr16 + 10747226 10747226 10747226 TATTGTCTGGGAAAGGCGGTGTTGGGAAAAGCACATTCAGCGCCCACCTTGCCCATGGCCTAGCA TATTGTCTGGGAAAGGCGGTGTTGGGAAAAGCGCATTCAGCGCCCACCTTGCCCATGGCCTAGCA A G NUBP1 Ensembl:ENSG00000103274 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:10747126..10747300 32194978 MeRIP-seq:(Medium) rs1455169565 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_22759767 Human_Splice_Rec_1677050,Human_Splice_Rec_1677051,Human_Splice_Rec_1677060,Human_Splice_Rec_1677061,Human_Splice_Rec_1677078,Human_Splice_Rec_1677079,Human_Splice_Rec_1677098,Human_Splice_Rec_1677099,Human_Splice_Rec_1677110,Human_Splice_Rec_1677111 Human_miRNA_ID_2237454,Human_miRNA_ID_2873768,Human_miRNA_ID_2981731 RMVar_hsa_circ_57286,RMVar_hsa_circ_296006,RMVar_hsa_circ_176204,RMVar_hsa_circ_44907 113174 RMVar_ID_113174 Human_SNP_ID_827516675 m1A Human chr16 + 67675235 67675235 67675235 GGGCTCCTCCGTCAGCACCTCCACAGCCTCCCACTCCCCGGATCGGCTCGACCTCTTGATGGCAT GGGCTCCTCCGTCAGCACCTCCACAGCCTCCCGCTCCCCGGATCGGCTCGACCTCTTGATGGCAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:67674630..67676026 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113175 RMVar_ID_113175 Human_SNP_ID_827529728 m1A Human chr16 + 30418171 30418171 30418171 CCGCTCCAACCTGGCGGAGCACGCGCGCACGCACACAGGCGAGCGGCCCTACCCCTGCGCCGAGT CCGCTCCAACCTGGCGGAGCACGCGCGCACGCGCACAGGCGAGCGGCCCTACCCCTGCGCCGAGT A G ZNF771 Ensembl:ENSG00000179965 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:30418122..30418205 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_4363564 113176 RMVar_ID_113176 Human_SNP_ID_827538167 m1A Human chr16 + 190134 190134 190134 TGACCGCCTCCGACGCCGATCCCGGGAGCGTGACCTGAACAATCAGAAGGCTCCAAGGCTGAGAC TGACCGCCTCCGACGCCGATCCCGGGAGCGTGGCCTGAACAATCAGAAGGCTCCAAGGCTGAGAC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:190101..190150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 113177 RMVar_ID_113177 Human_SNP_ID_827540502 m1A Human chr16 - 31473488 31473488 31473488 AGGCTCCGCAGGGCGCTCTTTGGGAGCCCCTGACCTTGGCATGTGCGAGGTGGTAGTCTCCAGGT AGGCTCCGCAGGGCGCTCTTTGGGAGCCCCTGGCCTTGGCATGTGCGAGGTGGTAGTCTCCAGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr16:31473412..31473518;chr16:31473486..31473612 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 113178 RMVar_ID_113178 Human_SNP_ID_827542156 m1A Human chr16 + 48339131 48339131 48339131 AGGTAGTCTAGAAGCAAGCCCTGAAGAACAGCATTATTTAGGGATCATATAGAGAGAAGAGGAGC AGGTAGTCTAGAAGCAAGCCCTGAAGAACAGCGTTATTTAGGGATCATATAGAGAGAAGAGGAGC A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:48339129..48339506 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_57064,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248,RMVar_hsa_circ_364069 113179 RMVar_ID_113179 Human_SNP_ID_827545085 m1A Human chr16 + 3731326 3731326 3731326 GCAGAGCGTGGACCACTTGGAGCGGCGCAAGGAGGAGAACTCCCAGTGCTTGTCTCTGGCGAGGG GCAGAGCGTGGACCACTTGGAGCGGCGCAAGGGGGAGAACTCCCAGTGCTTGTCTCTGGCGAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:3731278..3731417 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 113180 RMVar_ID_113180 Human_SNP_ID_827545466 m1A Human chr16 - 19009219 19009219 19009219 AATGGACCGGTAGCTTGGCAATTCTTGGAGGAAGTTCACAGGTGGAGAAGAGAAGCAACTGGAGT AATGGACCGGTAGCTTGGCAATTCTTGGAGGAGGTTCACAGGTGGAGAAGAGAAGCAACTGGAGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:19009136..19009226 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113181 RMVar_ID_113181 Human_SNP_ID_827549941 m1A Human chr16 - 70213219 70213219 70213219 TGTTTTGTGGGCAGGGGTAGATCTCACAAAGTACATTCTGAAGGGTGGGGAGAATTACAAAGGAC TGTTTTGTGGGCAGGGGTAGATCTCACAAAGTCCATTCTGAAGGGTGGGGAGAATTACAAAGGAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:70213117..70213251 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 113182 RMVar_ID_113182 Human_SNP_ID_827564795 m1A Human chr16 - 4340298 4340298 4340298 CCCCATACGTGACTGCTCGGCTCCCCCCGCCCACCCCGCCGCCTCTAATTTATAGCTTGGTAATA CCCCATACGTGACTGCTCGGCTCCCCCCGCCCCCCCCGCCGCCTCTAATTTATAGCTTGGTAATA T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs757243713 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_474031,Human_RBP_ID_17690327,Human_RBP_ID_17876829,Human_RBP_ID_26446808 Human_miRNA_ID_1702395,Human_miRNA_ID_1702396,Human_miRNA_ID_2146988,Human_miRNA_ID_2873765,Human_miRNA_ID_2981728,Human_miRNA_ID_2988414 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 113183 RMVar_ID_113183 Human_SNP_ID_827568226 m1A Human chr16 + 2761678 2761678 2761678 GACATGGCGGCTCCCCACAACCCCTTGCAACCACCCCCTTAAGCCAGGAGCCAGTGAACCCCCCA GACATGGCGGCTCCCCACAACCCCTTGCAACCCCCCCCTTAAGCCAGGAGCCAGTGAACCCCCCA A C SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:2761576..2761750 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_1003686,Human_RBP_ID_6505251,Human_RBP_ID_17077825,Human_RBP_ID_22052813,Human_RBP_ID_22199192,Human_RBP_ID_22800503,Human_RBP_ID_22937583 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 113184 RMVar_ID_113184 Human_SNP_ID_827575435 m1A Human chr16 + 681839 681839 681839 GCCAGCGAAACCACGAGGGTGATGAGGACGACAGCCACGTCCGGGCCCAGCAGGCCTGCATTGAG GCCAGCGAAACCACGAGGGTGATGAGGACGACCGCCACGTCCGGGCCCAGCAGGCCTGCATTGAG A C STUB1 Ensembl:ENSG00000103266 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:681774..681908 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_26328379,Human_RBP_ID_26949021 Human_Splice_Rec_1655708,Human_Splice_Rec_1655709,Human_Splice_Rec_1655720,Human_Splice_Rec_1655721,Human_Splice_Rec_1655730,Human_Splice_Rec_1655740,Human_Splice_Rec_1655741,Human_Splice_Rec_1655750,Human_Splice_Rec_1655756,Human_Splice_Rec_1655757,Human_Splice_Rec_1655766,Human_Splice_Rec_1655767,Human_Splice_Rec_1655774,Human_Splice_Rec_1655775,Human_Splice_Rec_1655780,Human_Splice_Rec_1655781 Human_miRNA_ID_1157614 113185 RMVar_ID_113185 Human_SNP_ID_827575588 m1A Human chr16 - 31183961 31183961 31183961 GTGCTGCTGGGAGCTGGCTGCTGGCCATAGCCAGGGTAGGAGGACTGCTGCCCGTAAGACGATTG GTGCTGCTGGGAGCTGGCTGCTGGCCATAGCCGGGGTAGGAGGACTGCTGCCCGTAAGACGATTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:31183911..31184049 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113186 RMVar_ID_113186 Human_SNP_ID_827575610 m1A Human chr16 + 31117781 31117781 31117781 CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGACCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG CCGGGCCCGGGGAGAATGCGGCCGCTGAGGGGCCCGCCCCATCCCCGGGCCGCGTCTCTCCGCCG A C KAT8 Ensembl:ENSG00000103510 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:31117732..31117846 26863196 MeRIP-seq:(Medium) rs1030164303 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_4393063,Human_RBP_ID_9325101,Human_RBP_ID_22441490,Human_RBP_ID_22532818,Human_RBP_ID_24552072,Human_RBP_ID_26769135 RMVar_hsa_circ_64374 113187 RMVar_ID_113187 Human_SNP_ID_827579486 m1A Human chr16 + 66550045 66550045 66550045 AGCAGCGCAGCGCCCGGGCGGCCCAGCCCCGCAGCGGCCACAGCAGCATAGCCGGGCGAGCGGAT AGCAGCGCAGCGCCCGGGCGGCCCAGCCCCGCGGCGGCCACAGCAGCATAGCCGGGCGAGCGGAT A G AC010542.4 Ensembl:ENSG00000261519 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:66549995..66550088 26863196 MeRIP-seq:(Medium) rs779367525 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113188 RMVar_ID_113188 Human_SNP_ID_827595645 m1A Human chr16 + 11782386 11782386 11782386 TGTTATCCCACACATCCACTTTCTAAATGAGCAATCTGGAAAGAAACAAGGCAAAAAAGCACATA TGTTATCCCACACATCCACTTTCTAAATGAGCGATCTGGAAAGAAACAAGGCAAAAAAGCACATA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr16:11782301..11782458 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 113189 RMVar_ID_113189 Human_SNP_ID_827601967 m1A Human chr16 - 74636579 74636579 74636579 AAGCTTTGTATTTATAAAATCTTTTTCATTTTAGGACTTGCAAAAACTTACGTCACATCAAAGTC AAGCTTTGTATTTATAAAATCTTTTTCATTTTCGGACTTGCAAAAACTTACGTCACATCAAAGTC T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74636551..74636600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_8810387,Human_RBP_ID_9285363,Human_RBP_ID_12811306,Human_RBP_ID_17255371 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_81650,RMVar_hsa_circ_179972,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_179975,RMVar_hsa_circ_310100,RMVar_hsa_circ_336224,RMVar_hsa_circ_179977,RMVar_hsa_circ_179979,RMVar_hsa_circ_373538,RMVar_hsa_circ_28231,RMVar_hsa_circ_179981,RMVar_hsa_circ_90685,RMVar_hsa_circ_299985,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179984,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_294256,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179990,RMVar_hsa_circ_179988 113190 RMVar_ID_113190 Human_SNP_ID_827615165 m1A Human chr16 - 35170181 35170181 35170181 GAAGAAGGAGGAGTAGTCGGCGGGAGGCACCAAGCGCAGCAGCAAGAAGGCGTCGGCGGCGCAGC GAAGAAGGAGGAGTAGTCGGCGGGAGGCACCACGCGCAGCAGCAAGAAGGCGTCGGCGGCGCAGC T G UBE2MP1 Ensembl:ENSG00000261461 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:35170131..35170255 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 113191 RMVar_ID_113191 Human_SNP_ID_827619689 m1A Human chr16 + 68530289 68530289 68530289 CCCTGCAACTAGCCTGCCGCTTCCCTCCCGGCACCCCCGCCGCCAGCCCCGAGCGCGGACCTGGA CCCTGCAACTAGCCTGCCGCTTCCCTCCCGGCCCCCCCGCCGCCAGCCCCGAGCGCGGACCTGGA A C ZFP90 Ensembl:ENSG00000184939 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:68530189..68530307 26863196 MeRIP-seq:(Medium) rs879604104 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_1731975,Human_Splice_Rec_1731981 113192 RMVar_ID_113192 Human_SNP_ID_827622781 m1A Human chr16 - 15029980 15029980 15029980 GCTTCCAGATCCATGACTGTGAGGCCGCTTGCAGGCACCAGCTGCTTCAGCTGTTCTCCCAGCTG GCTTCCAGATCCATGACTGTGAGGCCGCTTGCGGGCACCAGCTGCTTCAGCTGTTCTCCCAGCTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:15029951..15030025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_1512734,Human_RBP_ID_12672141 113193 RMVar_ID_113193 Human_SNP_ID_827627159 m1A Human chr16 - 1614847 1614847 1614847 GTGCTGGTCCTGGGGGCTGCCCTGCGGCGGGGACGGCGCCTGCGGCGCGCCGGGGGGCGCGGGGG GTGCTGGTCCTGGGGGCTGCCCTGCGGCGGGGGCGGCGCCTGCGGCGCGCCGGGGGGCGCGGGGG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr16:1614668..1614852 26863410 MeRIP-seq:(Medium) rs1396748134 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,lung small_cell_carcinoma 3 lung 113194 RMVar_ID_113194 Human_SNP_ID_827638251 m1A Human chr16 + 30979711 30979711 30979711 TGGAGCACAACTATGCCCTGGCCGTCAAGCCCACGCCCCCTGCGCCAGCCCTGCGGCCCCCGGAG TGGAGCACAACTATGCCCTGGCCGTCAAGCCCGCGCCCCCTGCGCCAGCCCTGCGGCCCCCGGAG A G SETD1A Ensembl:ENSG00000099381 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30979575..30980137 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_18678185 RMVar_hsa_circ_85722,RMVar_hsa_circ_177987 113195 RMVar_ID_113195 Human_SNP_ID_827639216 m1A Human chr16 - 72787739 72787715 72787739 TTCACGTCCCCACCGGCGGCGGCGGCGGTGGCAGTGGCGGCGGCGGCGGCGGTGGCGGCGGCGGC TTCACGTCCCCACCGGCGGCGGCGGCGGTGGC________________________GGCGGCGGC CGCCACCGCCGCCGCCGCCGCCACT C ZFHX3 Ensembl:ENSG00000140836 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA chr16:72787363..72787800;chr16:72787624..72787824;chr16:72787624..72787815 26863196 MeRIP-seq:(Medium) rs750348888 Functional Loss DEL ICGC 33..56 33 STAD 1 - Human_RBP_ID_125784,Human_RBP_ID_896052,Human_RBP_ID_5097627,Human_RBP_ID_5184219,Human_RBP_ID_8812812,Human_RBP_ID_17126229,Human_RBP_ID_17256751,Human_RBP_ID_17488855,Human_RBP_ID_17565492,Human_RBP_ID_17669785,Human_RBP_ID_17673406,Human_RBP_ID_19077802,Human_RBP_ID_22532829,Human_RBP_ID_23118708,Human_RBP_ID_24544741,Human_RBP_ID_24559045,Human_RBP_ID_26781084,Human_RBP_ID_27796878 113196 RMVar_ID_113196 Human_SNP_ID_827643059 m1A Human chr16 + 88715073 88715073 88715073 GTTGCAGCCCTCACTGGACCCCCTGCCGCCGTACATCCTGGCTGAGGCCCAGCTCCGCACACAGA GTTGCAGCCCTCACTGGACCCCCTGCCGCCGTGCATCCTGGCTGAGGCCCAGCTCCGCACACAGA A G CTU2 Ensembl:ENSG00000174177 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:88714608..88715287 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_762002,Human_RBP_ID_5114019,Human_RBP_ID_26810716 Human_Splice_Rec_1749568,Human_Splice_Rec_1749569,Human_Splice_Rec_1749622,Human_Splice_Rec_1749623,Human_Splice_Rec_1749650,Human_Splice_Rec_1749651,Human_Splice_Rec_1749686,Human_Splice_Rec_1749687,Human_Splice_Rec_1749702,Human_Splice_Rec_1749703 RMVar_hsa_circ_107942,RMVar_hsa_circ_180530 113197 RMVar_ID_113197 Human_SNP_ID_827645047 m1A Human chr16 - 85231127 85231127 85231127 ATCCATCCTTCCATCCATCCATCCATCCTTCCATCCATCCTTTCATCCATCCATTCATCTGTCCA ATCCATCCTTCCATCCATCCATCCATCCTTCCTTCCATCCTTTCATCCATCCATTCATCTGTCCA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:85231125..85231328 26863196 MeRIP-seq:(Medium) rs12598694 Functional Loss SNV ICGC 33..33 33 MELA 1 - 113198 RMVar_ID_113198 Human_SNP_ID_827651111 m1A Human chr16 - 89657637 89657637 89657637 TTCGATCGCCGCCGGGACCTGACACCGCCCGGAGTTGGCGTCCCTTCTCCCTCTCCGAGTGCTGC TTCGATCGCCGCCGGGACCTGACACCGCCCGGTGTTGGCGTCCCTTCTCCCTCTCCGAGTGCTGC T A CHMP1A Ensembl:ENSG00000131165 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89657576..89657675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_233628,Human_RBP_ID_4390860,Human_RBP_ID_9373428 Human_Splice_Rec_1753095,Human_Splice_Rec_1753107,Human_Splice_Rec_1753123,Human_Splice_Rec_1753135,Human_Splice_Rec_1753147,Human_Splice_Rec_1753157,Human_Splice_Rec_1753163 RMVar_hsa_circ_126095,RMVar_hsa_circ_180665 113199 RMVar_ID_113199 Human_SNP_ID_827667521 m1A Human chr16 + 30765058 30765058 30765058 GCTGCAGGAGAAACACCACCGCATCTCATTGGAGGTGAGGAGCCGGGGGCTTTGGGGGTGTGATT GCTGCAGGAGAAACACCACCGCATCTCATTGGCGGTGAGGAGCCGGGGGCTTTGGGGGTGTGATT A C RNF40 Ensembl:ENSG00000103549 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:30765007..30765278 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_Splice_Rec_1704153,Human_Splice_Rec_1704191,Human_Splice_Rec_1704207,Human_Splice_Rec_1704243,Human_Splice_Rec_1704283,Human_Splice_Rec_1704309 RMVar_hsa_circ_3934,RMVar_hsa_circ_57481,RMVar_hsa_circ_266434,RMVar_hsa_circ_53787 113200 RMVar_ID_113200 Human_SNP_ID_827671215 m1A Human chr16 - 84054421 84054421 84054421 TGTGACCGGCAGCCTGGCTGACCGTGAGGGCCAGAGAGAGCCTTCACGGACGGCGCTGGTGGGTG TGTGACCGGCAGCCTGGCTGACCGTGAGGGCCGGAGAGAGCCTTCACGGACGGCGCTGGTGGGTG T C MBTPS1 Ensembl:ENSG00000140943 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:84054376..84054425 32194978 MeRIP-seq:(Medium) rs2280026 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_8440198,Human_RBP_ID_18469929,Human_RBP_ID_18685426,Human_RBP_ID_27446080 113201 RMVar_ID_113201 Human_SNP_ID_827678930 m1A Human chr16 + 2206560 2206560 2206560 CTCCAATAACCCTAACCCCATCATCAGCTACGACGGCGTCAACAAGAACATCGCGTCTGTGGGCT CTCCAATAACCCTAACCCCATCATCAGCTACGTCGGCGTCAACAAGAACATCGCGTCTGTGGGCT A T MLST8 Ensembl:ENSG00000167965 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:2206510..2206633 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine tubulovillous,large_intestine adenocarcinoma,colon tubulovillous 12 large intestine Human_RBP_ID_470504,Human_RBP_ID_9060933,Human_RBP_ID_17873389,Human_RBP_ID_26809867,Human_RBP_ID_27440042 Human_Splice_Rec_1664868,Human_Splice_Rec_1664869,Human_Splice_Rec_1664880,Human_Splice_Rec_1664881,Human_Splice_Rec_1664896,Human_Splice_Rec_1664897,Human_Splice_Rec_1664912,Human_Splice_Rec_1664913,Human_Splice_Rec_1664923,Human_Splice_Rec_1664938,Human_Splice_Rec_1664944,Human_Splice_Rec_1664945,Human_Splice_Rec_1664954,Human_Splice_Rec_1664955,Human_Splice_Rec_1664964,Human_Splice_Rec_1664965,Human_Splice_Rec_1664977,Human_Splice_Rec_1664992,Human_Splice_Rec_1664993,Human_Splice_Rec_1665008,Human_Splice_Rec_1665014,Human_Splice_Rec_1665015,Human_Splice_Rec_1665024,Human_Splice_Rec_1665025,Human_Splice_Rec_1665038,Human_Splice_Rec_1665039,Human_Splice_Rec_1665046,Human_Splice_Rec_1665047,Human_Splice_Rec_1665066,Human_Splice_Rec_1665067,Human_Splice_Rec_1665078,Human_Splice_Rec_1665079,Human_Splice_Rec_1665092,Human_Splice_Rec_1665098,Human_Splice_Rec_1665099,Human_Splice_Rec_1665110,Human_Splice_Rec_1665111,Human_Splice_Rec_1665124,Human_Splice_Rec_1665125,Human_Splice_Rec_1665138,Human_Splice_Rec_1665139,Human_Splice_Rec_1665152,Human_Splice_Rec_1665153,Human_Splice_Rec_1665168,Human_Splice_Rec_1665169,Human_Splice_Rec_1665182,Human_Splice_Rec_1665183,Human_Splice_Rec_1665192,Human_Splice_Rec_1665193,Human_Splice_Rec_1665199 RMVar_hsa_circ_74780 113202 RMVar_ID_113202 Human_SNP_ID_827690255 m1A Human chr16 - 87708388 87708386 87708388 GGAGGTTGAGGGCGCCGAGGGTGGGGTCGACGACGAAGACAGCGGAGAGGAGAGCGGTGCGGAGG GGAGGTTGAGGGCGCCGAGGGTGGGGTCGACG__GAAGACAGCGGAGAGGAGAGCGGTGCGGAGG CGT C KLHDC4 Ensembl:ENSG00000104731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:87707951..87709421 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 LIHC 1 - Human_RBP_ID_44551,Human_RBP_ID_233555,Human_RBP_ID_892743,Human_RBP_ID_3949651,Human_RBP_ID_4388376,Human_RBP_ID_5114000,Human_RBP_ID_9373311,Human_RBP_ID_18987095,Human_RBP_ID_19075369,Human_RBP_ID_20169188,Human_RBP_ID_22583096,Human_RBP_ID_22712343,Human_RBP_ID_22944709,Human_RBP_ID_23118501,Human_RBP_ID_24544550,Human_RBP_ID_26329307,Human_RBP_ID_26780738 Human_Splice_Rec_1748370,Human_Splice_Rec_1748371,Human_Splice_Rec_1748381,Human_Splice_Rec_1748396,Human_Splice_Rec_1748397,Human_Splice_Rec_1748414,Human_Splice_Rec_1748415,Human_Splice_Rec_1748434,Human_Splice_Rec_1748435,Human_Splice_Rec_1748456,Human_Splice_Rec_1748457,Human_Splice_Rec_1748470,Human_Splice_Rec_1748471,Human_Splice_Rec_1748475,Human_Splice_Rec_1748494,Human_Splice_Rec_1748495,Human_Splice_Rec_1748514,Human_Splice_Rec_1748515 RMVar_hsa_circ_95917,RMVar_hsa_circ_300861,RMVar_hsa_circ_63705,RMVar_hsa_circ_65390,RMVar_hsa_circ_15052,RMVar_hsa_circ_180431 113203 RMVar_ID_113203 Human_SNP_ID_827691438 m1A Human chr16 + 1494301 1494301 1494301 TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGAGGTTCGACTCGCCGTCCGGGAAGCCATTCATG TCTGTCCTGCAGGATGGAGCCAGCACCCTCAGGGGTTCGACTCGCCGTCCGGGAAGCCATTCATG A G TELO2 Ensembl:ENSG00000100726 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2667661 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,skin basal_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 skin,head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_4393452 Human_Splice_Rec_1659484,Human_Splice_Rec_1659504 GWAS_ID_8862,GWAS_ID_8863 RMVar_hsa_circ_335860 113204 RMVar_ID_113204 Human_SNP_ID_827705343 m1A Human chr16 - 21300946 21300946 21300946 CCCAGCCCGCTTCATCTGCGCCCGCTGCCTTTACCCGCCAGCCACTCCGGCGTTTCCACCTCCGT CCCAGCCCGCTTCATCTGCGCCCGCTGCCTTTCCCCGCCAGCCACTCCGGCGTTTCCACCTCCGT T G CRYM Ensembl:ENSG00000103316 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:21300864..21301638 26863196 MeRIP-seq:(Medium) rs945965052 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113205 RMVar_ID_113205 Human_SNP_ID_827707317 m1A Human chr16 + 86508284 86508284 86508284 CTCTTCTCCCGCGAGCGCAGATCTGGCGGAGGAGGCGGCGACTGCCCGGCAGGCTGCGCCGGCGA CTCTTCTCCCGCGAGCGCAGATCTGGCGGAGGCGGCGGCGACTGCCCGGCAGGCTGCGCCGGCGA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:86508281..86508372 26863196 MeRIP-seq:(Medium) rs1204441179 Functional Loss SNV ICGC 33..33 33 LAML 1 - 113206 RMVar_ID_113206 Human_SNP_ID_827713492 m1A Human chr16 - 29885702 29885702 29885702 AGGGGGCAGCCCCCTATCCCCCGTGATCTATGATTCGGACATGGACGATGTCCCCGAGCGGGGTC AGGGGGCAGCCCCCTATCCCCCGTGATCTATGCTTCGGACATGGACGATGTCCCCGAGCGGGGTC T G SEZ6L2 Ensembl:ENSG00000174938 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr16:29885651..29885725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_17884099 Human_Splice_Rec_1700416,Human_Splice_Rec_1700450,Human_Splice_Rec_1700484,Human_Splice_Rec_1700516,Human_Splice_Rec_1700548,Human_Splice_Rec_1700572 Human_miRNA_ID_2534867,Human_miRNA_ID_2534868,Human_miRNA_ID_2534869,Human_miRNA_ID_2534870,Human_miRNA_ID_2536599,Human_miRNA_ID_2536600,Human_miRNA_ID_2536601,Human_miRNA_ID_2536602 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_325994,RMVar_hsa_circ_332823,RMVar_hsa_circ_114510,RMVar_hsa_circ_177790,RMVar_hsa_circ_177791 113207 RMVar_ID_113207 Human_SNP_ID_827714560 m1A Human chr16 - 69339839 69339839 69339839 CTCAAACATGACACGGGTCTCCTCTTCAGTCAAAGGCCGCATTTTTCCCCCTGGGTTGGAACACC CTCAAACATGACACGGGTCTCCTCTTCAGTCACAGGCCGCATTTTTCCCCCTGGGTTGGAACACC T G AC026464.3,AC026464.1 Ensembl:ENSG00000260371,Ensembl:ENSG00000259900 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:69339767..69340066 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 113208 RMVar_ID_113208 Human_SNP_ID_827718322 m1A Human chr16 + 30930213 30930213 30930213 GTGCCTGACACCTCCTCTTCCTCCTCGGACTCAGACTCCGACTCCGACTCTTCGGGCACATCGCT GTGCCTGACACCTCCTCTTCCTCCTCGGACTCCGACTCCGACTCCGACTCTTCGGGCACATCGCT A C FBXL19 Ensembl:ENSG00000099364 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:30930162..30930327 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_473179,Human_RBP_ID_8807311,Human_RBP_ID_9374237,Human_RBP_ID_27447969 RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 113209 RMVar_ID_113209 Human_SNP_ID_827725799 m1A Human chr16 + 23570949 23570947 23570949 ACAAGGGAATGATCAAAAGCTTTGTTTTTTTTAAAAAAAAAAAAAGCAGTTTCAATTGAAATATT ACAAGGGAATGATCAAAAGCTTTGTTTTTTT__AAAAAAAAAAAAGCAGTTTCAATTGAAATATT TTA T UBFD1 Ensembl:ENSG00000103353 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1491190198 Functional Loss DEL TCGA,ICGC 32..33 33 LMS,SARC,UCEC,ESCA 9 - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321,RMVar_hsa_circ_177324,RMVar_hsa_circ_108973 113210 RMVar_ID_113210 Human_SNP_ID_827745436 m1A Human chr16 - 28954684 28954684 28954684 GCTCCCAGGGCCCAAGGGCCCTGGCCTCACTCACAGAAACTCTGTCTTTTTCTTCTCTTCTTTAT GCTCCCAGGGCCCAAGGGCCCTGGCCTCACTCCCAGAAACTCTGTCTTTTTCTTCTCTTCTTTAT T G AC109460.2 Ensembl:ENSG00000260853 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:28954551..28954798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113211 RMVar_ID_113211 Human_SNP_ID_827748933 m1A Human chr16 + 764693 764693 764693 TCACCGGCTCTCTGAGCCCCCCGAGGACCTGGACGCCCTCCCATTGGACCTGCTGCTATTCCTCA TCACCGGCTCTCTGAGCCCCCCGAGGACCTGGGCGCCCTCCCATTGGACCTGCTGCTATTCCTCA A G MSLN Ensembl:ENSG00000102854 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:764605..764733 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate Human_Splice_Rec_1656630,Human_Splice_Rec_1656631,Human_Splice_Rec_1656664,Human_Splice_Rec_1656665,Human_Splice_Rec_1656696,Human_Splice_Rec_1656697,Human_Splice_Rec_1656728,Human_Splice_Rec_1656729,Human_Splice_Rec_1656760,Human_Splice_Rec_1656761,Human_Splice_Rec_1656780,Human_Splice_Rec_1656781 113212 RMVar_ID_113212 Human_SNP_ID_827754992 m1A Human chr16 - 19503326 19503326 19503326 ATGCAATAGTTGGTCACTGCATTTTTACCTGAACCAAAGCTAAACCCGGTGTTGCCACCATGCAC ATGCAATAGTTGGTCACTGCATTTTTACCTGACCCAAAGCTAAACCCGGTGTTGCCACCATGCAC T G GDE1 Ensembl:ENSG00000006007 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:19503275..19503524 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_469638,Human_RBP_ID_1003209,Human_RBP_ID_1513485,Human_RBP_ID_1839003,Human_RBP_ID_3492166,Human_RBP_ID_9060596,Human_RBP_ID_12681280,Human_RBP_ID_17255913,Human_RBP_ID_17485265,Human_RBP_ID_18284535,Human_RBP_ID_27237865,Human_RBP_ID_27439650,Human_RBP_ID_27559881 113213 RMVar_ID_113213 Human_SNP_ID_827764822 m1A Human chr16 - 797055 797055 797055 CCTCCCGGGCCGCTCGCCTCATGATGTGCTCCAGCCGCTGCTCATGGTTGCGTGGGGCAGGTCGG CCTCCCGGGCCGCTCGCCTCATGATGTGCTCCGGCCGCTGCTCATGGTTGCGTGGGGCAGGTCGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr16:797006..797123 26863196 MeRIP-seq:(Medium) rs765118548 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 113214 RMVar_ID_113214 Human_SNP_ID_827768380 m1A Human chr16 - 75000024 75000024 75000024 GTAGAGCATCCGCCAGCGAGGCTCGGGAGCCCAGGTACAGCATCCCGTCTCTATGGTGACCGCCG GTAGAGCATCCGCCAGCGAGGCTCGGGAGCCCCGGTACAGCATCCCGTCTCTATGGTGACCGCCG T G WDR59 Ensembl:ENSG00000103091 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:74999976..75000077 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic,face desmoplastic 4 skin,head and neck Human_Splice_Rec_1740535 113215 RMVar_ID_113215 Human_SNP_ID_827770933 m1A Human chr16 + 1961879 1961878 1961880 AGGCAGAGGATGCTGCAAGAGAGAAAAGCTGCAAAAGAGGCCGCCGCTGCCACCTCCTGAGGCAG AGGCAGAGGATGCTGCAAGAGAGAAAAGCTGC__AAGAGGCCGCCGCTGCCACCTCCTGAGGCAG CAA C NDUFB10 Ensembl:ENSG00000140990 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:1961828..1961926 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_469856,Human_RBP_ID_4354472,Human_RBP_ID_17652868,Human_RBP_ID_17883328,Human_RBP_ID_23681820,Human_RBP_ID_26439758,Human_RBP_ID_26939612,Human_RBP_ID_27237998 Human_Splice_Rec_1661056,Human_Splice_Rec_1661068,Human_Splice_Rec_1661074 Human_miRNA_ID_204763,Human_miRNA_ID_1489459,Human_miRNA_ID_2013431,Human_miRNA_ID_2759823 RMVar_hsa_circ_80934,RMVar_hsa_circ_91180,RMVar_hsa_circ_175581,RMVar_hsa_circ_85293,RMVar_hsa_circ_175582,RMVar_hsa_circ_175583 113216 RMVar_ID_113216 Human_SNP_ID_827779302 m1A Human chr16 - 74463414 74463414 74463414 TTGCAGTGCTTGAAGCAAAATAAAAACAGTGAATTGATGGATCCCAAATGCAAACAGATGATAAC TTGCAGTGCTTGAAGCAAAATAAAAACAGTGAGTTGATGGATCCCAAATGCAAACAGATGATAAC T C GLG1 Ensembl:ENSG00000090863 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:74463363..74465710 32194978 MeRIP-seq:(Medium) rs200712036 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_1846503,Human_RBP_ID_12809485 Human_Splice_Rec_1739862,Human_Splice_Rec_1739863,Human_Splice_Rec_1739914,Human_Splice_Rec_1739915,Human_Splice_Rec_1739962,Human_Splice_Rec_1739963,Human_Splice_Rec_1740004,Human_Splice_Rec_1740005,Human_Splice_Rec_1740056,Human_Splice_Rec_1740057,Human_Splice_Rec_1740076,Human_Splice_Rec_1740079 Human_miRNA_ID_3063281 RMVar_hsa_circ_20809,RMVar_hsa_circ_121633,RMVar_hsa_circ_179935,RMVar_hsa_circ_23793,RMVar_hsa_circ_54318,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_67270,RMVar_hsa_circ_75482,RMVar_hsa_circ_64890,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_179940,RMVar_hsa_circ_11610,RMVar_hsa_circ_179944,RMVar_hsa_circ_115672,RMVar_hsa_circ_305269,RMVar_hsa_circ_321638,RMVar_hsa_circ_345084,RMVar_hsa_circ_292548,RMVar_hsa_circ_179946,RMVar_hsa_circ_179945,RMVar_hsa_circ_297579,RMVar_hsa_circ_179942,RMVar_hsa_circ_179943,RMVar_hsa_circ_323969,RMVar_hsa_circ_318392,RMVar_hsa_circ_276518,RMVar_hsa_circ_294160,RMVar_hsa_circ_104398,RMVar_hsa_circ_179951,RMVar_hsa_circ_179952,RMVar_hsa_circ_179953,RMVar_hsa_circ_179950,RMVar_hsa_circ_27971,RMVar_hsa_circ_29687,RMVar_hsa_circ_22097,RMVar_hsa_circ_357120,RMVar_hsa_circ_11749,RMVar_hsa_circ_24809,RMVar_hsa_circ_340694,RMVar_hsa_circ_179954 113217 RMVar_ID_113217 Human_SNP_ID_827788415 m1A Human chr16 + 2768091 2768036 2768092 GCCTCTACTGGGGCCCAGCAGCCTTCTGCATTAGCCGCCCTGCAGCCAGCAAAGGAGCGGCGGAG __________________________________CCGCCCTGCAGCCAGCAAAGGAGCGGCGGAG ACTCTGATGTGGGGGAGCCACCTGCCTCTACTGGGGCCCAGCAGCCTTCTGCATTAG A SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:2768046..2768174 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 1..34 33 UCEC 1 - Human_RBP_ID_471605,Human_RBP_ID_818620,Human_RBP_ID_1177618,Human_RBP_ID_1840866,Human_RBP_ID_8431246,Human_RBP_ID_8806584,Human_RBP_ID_17077829,Human_RBP_ID_17253766,Human_RBP_ID_17485940,Human_RBP_ID_18676706,Human_RBP_ID_20093690,Human_RBP_ID_22049339,Human_RBP_ID_22199324,Human_RBP_ID_22800630,Human_RBP_ID_22937791,Human_RBP_ID_24475946,Human_RBP_ID_26941779,Human_RBP_ID_27239759 Human_miRNA_ID_2332594,Human_miRNA_ID_2965680 RMVar_hsa_circ_101161,RMVar_hsa_circ_175807,RMVar_hsa_circ_78249,RMVar_hsa_circ_175808,RMVar_hsa_circ_77021,RMVar_hsa_circ_125427,RMVar_hsa_circ_175811,RMVar_hsa_circ_85763,RMVar_hsa_circ_175812,RMVar_hsa_circ_175813,RMVar_hsa_circ_112243,RMVar_hsa_circ_175816,RMVar_hsa_circ_175817,RMVar_hsa_circ_96171,RMVar_hsa_circ_265651 113218 RMVar_ID_113218 Human_SNP_ID_827794617 m1A Human chr16 - 2603497 2603497 2603497 ACCCCGCCCCGAGCCTGCCACGGGCCAGCGGCAGGAGCTCGCAGTGATTCCCCGCCATGATCCCA ACCCCGCCCCGAGCCTGCCACGGGCCAGCGGCGGGAGCTCGCAGTGATTCCCCGCCATGATCCCA T C lnc-CEMP1-10 RNACentral:URS00008B7AF1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:2603447..2603691 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113219 RMVar_ID_113219 Human_SNP_ID_827805668 m1A Human chr16 - 534196 534196 534196 GGGACCCCGGGCCGCCCTCACCGTCGCCTCCCACGACAGGACCACGGCCCAAACGGCTGGGAGAA GGGACCCCGGGCCGCCCTCACCGTCGCCTCCCGCGACAGGACCACGGCCCAAACGGCTGGGAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:534193..534289 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 113220 RMVar_ID_113220 Human_SNP_ID_827815262 m1A Human chr16 + 46972941 46972941 46972941 GCTACCTCCGGGTCAATGGGCGAGGGACGCAGAGAGGGAGGAGCTCCCGCAGCCGGCGGCCGCGG GCTACCTCCGGGTCAATGGGCGAGGGACGCAGGGAGGGAGGAGCTCCCGCAGCCGGCGGCCGCGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr16:46972938..46973639 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113221 RMVar_ID_113221 Human_SNP_ID_827826917 m1A Human chr16 + 68236019 68236019 68236019 GCGGGGTCGGCCGCGGGGTCAGGGCCCGGGGGAGGGGGCGGCGGCGGCGGCGGAGTCATGGCCGC GCGGGGTCGGCCGCGGGGTCAGGGCCCGGGGGGGGGGGCGGCGGCGGCGGCGGAGTCATGGCCGC A G L13708-001 RNACentral:URS000039574C misc_RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:68235979..68236091 26863196 MeRIP-seq:(Medium) rs997886751 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113222 RMVar_ID_113222 Human_SNP_ID_827827854 m1A Human chr16 - 89280498 89280498 89280498 CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTACCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG CCCAGGGCCCTTCAGCGCCTCGGAGGCGCCGTCCCCCGCCCCTCCCGCCTCTCCTGCCCCGTACG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:89280423..89280669 26863196 MeRIP-seq:(Medium) rs770628197 Functional Loss SNV ICGC,COSMIC 33..33 33 THCA,head_neck squamous_cell_carcinoma 22 head and neck Human_RBP_ID_17371570,Human_RBP_ID_22715540,Human_RBP_ID_27447325 Human_miRNA_ID_167063,Human_miRNA_ID_464597,Human_miRNA_ID_2147114,Human_miRNA_ID_2387186,Human_miRNA_ID_2388659,Human_miRNA_ID_2390896,Human_miRNA_ID_2399807,Human_miRNA_ID_2592142,Human_miRNA_ID_2988539,Human_miRNA_ID_3022240,Human_miRNA_ID_3030864 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_354647,RMVar_hsa_circ_180605,RMVar_hsa_circ_269582 113223 RMVar_ID_113223 Human_SNP_ID_827828603 m1A Human chr16 + 56748305 56748305 56748305 TCCTTCAGCAAGCTGAACAGCTTGCTGCTGAGACTGAGGGCATCTCAGAGCTTCCCCATGTGGAA TCCTTCAGCAAGCTGAACAGCTTGCTGCTGAGCCTGAGGGCATCTCAGAGCTTCCCCATGTGGAA A C NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr16:56748202..56748327 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_3947687,Human_RBP_ID_4393855,Human_RBP_ID_5358144,Human_RBP_ID_9286301,Human_RBP_ID_9325134,Human_RBP_ID_18680904,Human_RBP_ID_18983802 Human_Splice_Rec_1715950,Human_Splice_Rec_1715966,Human_Splice_Rec_1715974,Human_Splice_Rec_1716016,Human_Splice_Rec_1716078 RMVar_hsa_circ_25462,RMVar_hsa_circ_85420,RMVar_hsa_circ_22527,RMVar_hsa_circ_178590,RMVar_hsa_circ_321734,RMVar_hsa_circ_349228,RMVar_hsa_circ_178591 113224 RMVar_ID_113224 Human_SNP_ID_827834938 m1A Human chr16 - 4614832 4614832 4614832 ATGGTGGACGCGTGAGGCGGAGGCGCGGGCGGAGGAGGGAGGCCGGAGCGGGCAGCGCGGCGGCG ATGGTGGACGCGTGAGGCGGAGGCGCGGGCGGCGGAGGGAGGCCGGAGCGGGCAGCGCGGCGGCG T G UBALD1 Ensembl:ENSG00000153443 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:4614651..4614875 26863196 MeRIP-seq:(Medium) rs860889 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_234936,Human_RBP_ID_763743,Human_RBP_ID_3506906,Human_RBP_ID_4400506,Human_RBP_ID_5113857,Human_RBP_ID_5141827,Human_RBP_ID_5316562,Human_RBP_ID_8084775,Human_RBP_ID_8726138,Human_RBP_ID_9324925,Human_RBP_ID_9419643,Human_RBP_ID_17371635,Human_RBP_ID_18162067,Human_RBP_ID_18418656,Human_RBP_ID_18482156,Human_RBP_ID_22713015,Human_RBP_ID_22738185,Human_RBP_ID_23118575,Human_RBP_ID_26779177,Human_RBP_ID_27837781 Human_Splice_Rec_1672495 113225 RMVar_ID_113225 Human_SNP_ID_827844177 m1A Human chr16 - 84618026 84618026 84618026 TCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCACCGCCGCCAGCCCGTGCGCCCTCGGCGCGTAC TCGCAGCTTGCAGGCGCCGCGTAGCCGTCGCCGCCGCCGCCAGCCCGTGCGCCCTCGGCGCGTAC T C COTL1 Ensembl:ENSG00000103187 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:84617851..84618075;chr16:84617803..84618075;chr16:84617788..84618075 26863196 MeRIP-seq:(Medium) rs959891765 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_233378,Human_RBP_ID_4386644 RMVar_hsa_circ_108047,RMVar_hsa_circ_180315 113226 RMVar_ID_113226 Human_SNP_ID_827845839 m1A Human chr16 + 89873668 89873668 89873668 CCTCTCTCCAGACGTCGTGGTCGTTCGGTCCTATGTCGCGCCGGGCCCTCCGGAGGCTGAGGGGG CCTCTCTCCAGACGTCGTGGTCGTTCGGTCCTGTGTCGCGCCGGGCCCTCCGGAGGCTGAGGGGG A G TCF25 Ensembl:ENSG00000141002 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr16:89873632..89873769 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine Human_RBP_ID_44937,Human_RBP_ID_4405054,Human_RBP_ID_8726437,Human_RBP_ID_18688145,Human_RBP_ID_22208448,Human_RBP_ID_26953449,Human_RBP_ID_27812108 RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779 113227 RMVar_ID_113227 Human_SNP_ID_827848830 m1A Human chr16 + 89873824 89873824 89873824 AGCTTGGTGTCCGGCGTCCCGGGGGCGCAGGGAAGGAGGGCGTCCGAGTCAACAACCGCTTCGAG AGCTTGGTGTCCGGCGTCCCGGGGGCGCAGGGCAGGAGGGCGTCCGAGTCAACAACCGCTTCGAG A C TCF25 Ensembl:ENSG00000141002 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr16:89873776..89873969 26863196 MeRIP-seq:(Medium) rs13338056 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_818417,Human_RBP_ID_3948224,Human_RBP_ID_18987427,Human_RBP_ID_22441195,Human_RBP_ID_26329502,Human_RBP_ID_27812109 Human_Splice_Rec_1754331,Human_Splice_Rec_1754369,Human_Splice_Rec_1754405,Human_Splice_Rec_1754407,Human_Splice_Rec_1754441,Human_Splice_Rec_1754453,Human_Splice_Rec_1754463,Human_Splice_Rec_1754465,Human_Splice_Rec_1754477,Human_Splice_Rec_1754485 RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779 113228 RMVar_ID_113228 Human_SNP_ID_827853174 m1A Human chr16 + 47461331 47461331 47461331 ATTGCTGACAGGCGGCCCCGGGGGCGGTGGCCAAGGCGGCGACCGGAGCGCGATGGCGGGGGCGG ATTGCTGACAGGCGGCCCCGGGGGCGGTGGCCGAGGCGGCGACCGGAGCGCGATGGCGGGGGCGG A G PHKB Ensembl:ENSG00000102893 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr16:47461322..47461456 26863196 MeRIP-seq:(Medium) rs748523564 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4394703,Human_RBP_ID_5317559,Human_RBP_ID_22944653 Human_Splice_Rec_1708633,Human_Splice_Rec_1708647,Human_Splice_Rec_1708709,Human_Splice_Rec_1708769,Human_Splice_Rec_1708771,Human_Splice_Rec_1708773,Human_Splice_Rec_1708833,Human_Splice_Rec_1708853 RMVar_hsa_circ_178161,RMVar_hsa_circ_121637 113229 RMVar_ID_113229 Human_SNP_ID_827860050 m1A Human chr16 - 3770722 3770722 3770722 CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTACCCAAACCCAGAGCACCCCTACAGTCCAGGCA CCACCCCGACTCCTGGCTCAGTGCCCAGTGCTGCCCAAACCCAGAGCACCCCTACAGTCCAGGCA T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr16:3770551..3770900 26863196 MeRIP-seq:(Medium) rs143247685 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue myelodysplastic_syndrome 2 haematopoietic and lymphoid tissue Human_RBP_ID_9285597,Human_RBP_ID_17256578,Human_RBP_ID_17488358,Human_RBP_ID_18679223,Human_RBP_ID_26328586 Human_miRNA_ID_2425014,Human_miRNA_ID_2434676,Human_miRNA_ID_2908180,Human_miRNA_ID_3027019 Clinvar_Rec_326,Clinvar_Rec_327 RMVar_hsa_circ_12577,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,RMVar_hsa_circ_320859,RMVar_hsa_circ_307611,RMVar_hsa_circ_175928,RMVar_hsa_circ_327565,RMVar_hsa_circ_175931,RMVar_hsa_circ_114949,RMVar_hsa_circ_360705,RMVar_hsa_circ_128142,RMVar_hsa_circ_175935,RMVar_hsa_circ_175936,RMVar_hsa_circ_109495,RMVar_hsa_circ_356220,RMVar_hsa_circ_175937,RMVar_hsa_circ_175938 113230 RMVar_ID_113230 Human_SNP_ID_827860398 m1A Human chr16 + 10547622 10547622 10547622 CGATGATGAAAGCAAGAAGCACCAACATTTTCACAGGGCAGGGCGAGTCGAGGCGAGGGGTCACG CGATGATGAAAGCAAGAAGCACCAACATTTTCGCAGGGCAGGGCGAGTCGAGGCGAGGGGTCACG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr16:10547551..10547728 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113231 RMVar_ID_113231 Human_SNP_ID_827863820 m1A Human chr16 - 70664360 70664360 70664360 AGTTTGACAAGTCATCCACCATCCCGCGCAACAGCAACATCGCCCAGAACTACCGCCGCCTGATC AGTTTGACAAGTCATCCACCATCCCGCGCAACGGCAACATCGCCCAGAACTACCGCCGCCTGATC T C MTSS2 Ensembl:ENSG00000132613 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr16:70664009..70664440;chr16:70663960..70664403;chr16:70664041..70664403;chr16:70664043..70664382 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach RMVar_hsa_circ_115261,RMVar_hsa_circ_179708 113232 RMVar_ID_113232 Human_SNP_ID_827867231 m1A Human chr16 - 29994141 29994141 29994141 GGGTGGGAAGAGGTTGAGTGGAAGCAGCGAGGACGAGGAAGACAGTGGGAAGGGGGAACCCACAG GGGTGGGAAGAGGTTGAGTGGAAGCAGCGAGGGCGAGGAAGACAGTGGGAAGGGGGAACCCACAG T C HIRIP3 Ensembl:ENSG00000149929 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr16:29994046..29994644 26863196 MeRIP-seq:(Medium) rs967815547 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4362404,Human_RBP_ID_6507270,Human_RBP_ID_17067826,Human_RBP_ID_23686286,Human_RBP_ID_26328876 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 113233 RMVar_ID_113233 Human_SNP_ID_844856814 m1A Human chr3 + 58126713 58126713 58126713 GGCAGCTGCAGTGCTGAGTACATTCCTTTCGCACCGGGGGATTACGATGTTAATATCACATATGG GGCAGCTGCAGTGCTGAGTACATTCCTTTCGCGCCGGGGGATTACGATGTTAATATCACATATGG A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2362903 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,thyroid neoplasm,COCA 15 head and neck,breast Human_RBP_ID_67586,Human_RBP_ID_8874038,Human_RBP_ID_9261136 Human_Splice_Rec_445859,Human_Splice_Rec_445951,Human_Splice_Rec_446039,Human_Splice_Rec_446129,Human_Splice_Rec_446217 Clinvar_Rec_484 GWAS_ID_10845 RMVar_hsa_circ_1339,RMVar_hsa_circ_118736,RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168,RMVar_hsa_circ_90360,RMVar_hsa_circ_96548,RMVar_hsa_circ_64555,RMVar_hsa_circ_77922,RMVar_hsa_circ_12329,RMVar_hsa_circ_9008,RMVar_hsa_circ_219171,RMVar_hsa_circ_219172,RMVar_hsa_circ_219169,RMVar_hsa_circ_219170,RMVar_hsa_circ_116455,RMVar_hsa_circ_219179,RMVar_hsa_circ_85416,RMVar_hsa_circ_219182,RMVar_hsa_circ_122972,RMVar_hsa_circ_219186,RMVar_hsa_circ_94948,RMVar_hsa_circ_265588,RMVar_hsa_circ_219187,RMVar_hsa_circ_91076,RMVar_hsa_circ_219188,RMVar_hsa_circ_119463,RMVar_hsa_circ_89259,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_269448,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_295896,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_126525,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219203,RMVar_hsa_circ_219206,RMVar_hsa_circ_115414,RMVar_hsa_circ_219207,RMVar_hsa_circ_219208,RMVar_hsa_circ_83988,RMVar_hsa_circ_219212,RMVar_hsa_circ_78034,RMVar_hsa_circ_219213,RMVar_hsa_circ_126764,RMVar_hsa_circ_65074,RMVar_hsa_circ_20161,RMVar_hsa_circ_219214,RMVar_hsa_circ_219215,RMVar_hsa_circ_276002,RMVar_hsa_circ_123318,RMVar_hsa_circ_45616,RMVar_hsa_circ_128181,RMVar_hsa_circ_62470,RMVar_hsa_circ_219216,RMVar_hsa_circ_219217,RMVar_hsa_circ_362730,RMVar_hsa_circ_114091,RMVar_hsa_circ_356300,RMVar_hsa_circ_369422,RMVar_hsa_circ_353500,RMVar_hsa_circ_76358,RMVar_hsa_circ_219219,RMVar_hsa_circ_219220,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_287080,RMVar_hsa_circ_268944,RMVar_hsa_circ_219223,RMVar_hsa_circ_76324,RMVar_hsa_circ_92411,RMVar_hsa_circ_219225,RMVar_hsa_circ_219226,RMVar_hsa_circ_219224,RMVar_hsa_circ_85139,RMVar_hsa_circ_93933,RMVar_hsa_circ_219228,RMVar_hsa_circ_219229 113234 RMVar_ID_113234 Human_SNP_ID_844884926 m1A Human chr3 - 186783632 186783632 186783632 CCGCGACCGCCAACAGACTGCATACCTGTTATAATCCGCGGAGCCACCAGACATGATCCGAAAAA CCGCGACCGCCAACAGACTGCATACCTGTTATGATCCGCGGAGCCACCAGACATGATCCGAAAAA T C AC112907.3 Ensembl:ENSG00000263826 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:186783628..186783729 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113235 RMVar_ID_113235 Human_SNP_ID_844942257 m1A Human chr3 - 158684584 158684584 158684584 AACCATGTGGTGTGCTCCATCTTGCAGGACAAACCGGAGCCCAGAGAGCTTGTGACCAGAAAGAG AACCATGTGGTGTGCTCCATCTTGCAGGACAACCCGGAGCCCAGAGAGCTTGTGACCAGAAAGAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:158684536..158684637 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain 113236 RMVar_ID_113236 Human_SNP_ID_844948537 m1A Human chr3 + 98797038 98797035 98797038 GCCGTATATGTATCAGACATATAAATGTAGTAAAAAAAAAAAAAAAAAAAATAGAAAACCTCTAC GCCGTATATGTATCAGACATATAAATGTAG___AAAAAAAAAAAAAAAAAATAGAAAACCTCTAC GTAA G ST3GAL6 Ensembl:ENSG00000064225 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:98796938..98797038 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 SKCA 1 - RMVar_hsa_circ_219938,RMVar_hsa_circ_219940 113237 RMVar_ID_113237 Human_SNP_ID_844950018 m1A Human chr3 + 9893149 9893149 9893149 AGCTACCTGGTGCTCTCCATGATCAGCATGGGACTCTTTTCCATCGCTCCACTCATTTATGGCAG AGCTACCTGGTGCTCTCCATGATCAGCATGGGTCTCTTTTCCATCGCTCCACTCATTTATGGCAG A T JAGN1 Ensembl:ENSG00000171135 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:9893099..9893450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1970797,Human_RBP_ID_8580815,Human_RBP_ID_14971137,Human_RBP_ID_17291154,Human_RBP_ID_17521339,Human_RBP_ID_18012532,Human_RBP_ID_18816150,Human_RBP_ID_22286455,Human_RBP_ID_22768497,Human_RBP_ID_26823547,Human_RBP_ID_27322966,Human_RBP_ID_27505092 113238 RMVar_ID_113238 Human_SNP_ID_844964215 m1A Human chr3 + 50252348 50252348 50252348 AGCAGGTCCCAGTAGCCCCAGGCAGCCGTGGGAACTCCCAGTGCCCAGGGGACACTAACCTTCCT AGCAGGTCCCAGTAGCCCCAGGCAGCCGTGGGGACTCCCAGTGCCCAGGGGACACTAACCTTCCT A G GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:50252346..50252550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUSC 1 - Human_RBP_ID_22551595 RMVar_hsa_circ_127577,RMVar_hsa_circ_117551,RMVar_hsa_circ_308775,RMVar_hsa_circ_218410,RMVar_hsa_circ_327248,RMVar_hsa_circ_304563,RMVar_hsa_circ_218412,RMVar_hsa_circ_218414,RMVar_hsa_circ_84841,RMVar_hsa_circ_218415,RMVar_hsa_circ_218413,RMVar_hsa_circ_218411 113239 RMVar_ID_113239 Human_SNP_ID_844995217 m1A Human chr3 + 49022909 49022909 49022909 GATCGTGGTGGTGGGGACTGGAGACCGGACCGAGAGGCTGCAGTCCCAGGTGCTTCAAGCCATGA GATCGTGGTGGTGGGGACTGGAGACCGGACCGGGAGGCTGCAGTCCCAGGTGCTTCAAGCCATGA A G NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:49022876..49023000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine Human_RBP_ID_248613,Human_RBP_ID_603966,Human_RBP_ID_14863347,Human_RBP_ID_18007174,Human_RBP_ID_18810251,Human_RBP_ID_19010278,Human_RBP_ID_19115464 Human_Splice_Rec_427080,Human_Splice_Rec_427081,Human_Splice_Rec_427088,Human_Splice_Rec_427089,Human_Splice_Rec_427096,Human_Splice_Rec_427097,Human_Splice_Rec_427102,Human_Splice_Rec_427103,Human_Splice_Rec_427114,Human_Splice_Rec_427115 113240 RMVar_ID_113240 Human_SNP_ID_845002614 m1A Human chr3 + 50256177 50256177 50256177 GAAGCCCCATGCTGGCCCCCACTGACCCTCCCACCCCCCATCCCCAGCTACCTGAACGACCTGGA GAAGCCCCATGCTGGCCCCCACTGACCCTCCCCCCCCCCATCCCCAGCTACCTGAACGACCTGGA A C GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50256176..50256200 32194978 MeRIP-seq:(Medium) rs782374342 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_127577,RMVar_hsa_circ_327248,RMVar_hsa_circ_218412,RMVar_hsa_circ_84841,RMVar_hsa_circ_218413,RMVar_hsa_circ_218411 113241 RMVar_ID_113241 Human_SNP_ID_845007428 m1A Human chr3 + 53882103 53882103 53882103 TCTCCGTATCACCCTTCTCAGCCTGGGTCATTATGGCCGGAGACACCCACCAACCTCTCGCCTCA TCTCCGTATCACCCTTCTCAGCCTGGGTCATTGTGGCCGGAGACACCCACCAACCTCTCGCCTCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:53881993..53882152 26863196 MeRIP-seq:(Medium) rs2276845 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 6 large intestine GWAS_ID_10816,GWAS_ID_10817,GWAS_ID_10818,GWAS_ID_10819,GWAS_ID_10820,GWAS_ID_10821,GWAS_ID_10822,GWAS_ID_10823,GWAS_ID_10824,GWAS_ID_10825,GWAS_ID_10826,GWAS_ID_10827,GWAS_ID_10828,GWAS_ID_10829,GWAS_ID_10830,GWAS_ID_10831,GWAS_ID_10832,GWAS_ID_10833,GWAS_ID_10834,GWAS_ID_10835,GWAS_ID_10836,GWAS_ID_10837,GWAS_ID_10838,GWAS_ID_10839,GWAS_ID_10840 113242 RMVar_ID_113242 Human_SNP_ID_845022098 m1A Human chr3 + 150546373 150546373 150546373 GACCGAGCGGGGCAGGTGCGCAGGAGGAAGAGAACTGGCCGCCGGGTCGTTCTCGCGCCGCCGTC GACCGAGCGGGGCAGGTGCGCAGGAGGAAGAGCACTGGCCGCCGGGTCGTTCTCGCGCCGCCGTC A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:150546051..150546525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113243 RMVar_ID_113243 Human_SNP_ID_845025988 m1A Human chr3 - 50340684 50340684 50340684 CGCGCTGCGCATCGCGCGGGGCACCGCGTGCAACCCCACACGGCAGCTGGTCCCTGGCCGTGGCC CGCGCTGCGCATCGCGCGGGGCACCGCGTGCACCCCCACACGGCAGCTGGTCCCTGGCCGTGGCC T G RASSF1 Ensembl:ENSG00000068028 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:50340652..50340778 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113244 RMVar_ID_113244 Human_SNP_ID_845034436 m1A Human chr3 - 52199282 52199282 52199282 ATTTGCCTGCTTTCTGCAGAAAGGCCTGGGGGACTCGGGATAAGAATGGGCAGCGGCGAACAACA ATTTGCCTGCTTTCTGCAGAAAGGCCTGGGGGCCTCGGGATAAGAATGGGCAGCGGCGAACAACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52199236..52199390 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 113245 RMVar_ID_113245 Human_SNP_ID_845057140 m1A Human chr3 - 50264241 50264241 50264241 CTCCTCTCTTGTCCCCTTTTGCTGTGCCCCTCACCCCAGTACTTTTTTTTTTCTTCTTTTTTTTG CTCCTCTCTTGTCCCCTTTTGCTGTGCCCCTCCCCCCAGTACTTTTTTTTTTCTTCTTTTTTTTG T G lnc-HYAL3-1 RNACentral:URS00008BE585 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50264234..50264310 26863196 MeRIP-seq:(Medium) rs1222142362 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 113246 RMVar_ID_113246 Human_SNP_ID_845057496 m1A Human chr3 - 51989032 51989032 51989032 TGGGCAGGGCAGGCACACTGGCAAGGGCAGGCAGCAGGCGTGTATATATGTCCACCCCACGGAGG TGGGCAGGGCAGGCACACTGGCAAGGGCAGGCGGCAGGCGTGTATATATGTCCACCCCACGGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51988984..51989141 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_7208696 113247 RMVar_ID_113247 Human_SNP_ID_845060710 m1A Human chr3 + 186784693 186784693 186784693 CTATTCAGCAGAGAGCTATTATTCCCTGTATTAAAGGTAAAAGAAACTGGCATTTTTAGGAAATT CTATTCAGCAGAGAGCTATTATTCCCTGTATTTAAGGTAAAAGAAACTGGCATTTTTAGGAAATT A T EIF4A2 Ensembl:ENSG00000156976 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186784426..186784715 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 2 skin,head and neck Human_RBP_ID_1958255,Human_RBP_ID_2807312,Human_RBP_ID_5391157,Human_RBP_ID_8567699,Human_RBP_ID_19116485,Human_RBP_ID_23213679,Human_RBP_ID_27716325 Human_Splice_Rec_521745,Human_Splice_Rec_521751,Human_Splice_Rec_521777,Human_Splice_Rec_521783,Human_Splice_Rec_521789,Human_Splice_Rec_521795,Human_Splice_Rec_521813,Human_Splice_Rec_521835,Human_Splice_Rec_521855,Human_Splice_Rec_521881,Human_Splice_Rec_521893,Human_Splice_Rec_521909,Human_Splice_Rec_521915 Human_miRNA_ID_1130855,Human_miRNA_ID_2531948,Human_miRNA_ID_2983038 RMVar_hsa_circ_122792,RMVar_hsa_circ_85571,RMVar_hsa_circ_223573,RMVar_hsa_circ_57867,RMVar_hsa_circ_283977,RMVar_hsa_circ_314198,RMVar_hsa_circ_223574,RMVar_hsa_circ_341683,RMVar_hsa_circ_298549,RMVar_hsa_circ_58834,RMVar_hsa_circ_223575,RMVar_hsa_circ_223576 113248 RMVar_ID_113248 Human_SNP_ID_845069018 m1A Human chr3 - 134222527 134222527 134222527 TTTTTCCTATTTTTTTCTAGGTCTTGATGCAGAACTTTATTATGTGAGAAATGACCTTATTAGTC TTTTTCCTATTTTTTTCTAGGTCTTGATGCAGGACTTTATTATGTGAGAAATGACCTTATTAGTC T C RYK Ensembl:ENSG00000163785 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:134222476..134222550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_22676685,Human_RBP_ID_25763181 Human_Splice_Rec_486062,Human_Splice_Rec_486088,Human_Splice_Rec_486124 Human_miRNA_ID_2062457,Human_miRNA_ID_2900127 RMVar_hsa_circ_299615,RMVar_hsa_circ_221472,RMVar_hsa_circ_310934,RMVar_hsa_circ_221485,RMVar_hsa_circ_17865,RMVar_hsa_circ_308685,RMVar_hsa_circ_221491,RMVar_hsa_circ_280693 113249 RMVar_ID_113249 Human_SNP_ID_845085506 m1A Human chr3 + 184149818 184149818 184149818 AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGATGCAAGTTACACCAACCAGGACAGAAATCATT AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGGTGCAAGTTACACCAACCAGGACAGAAATCATT A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1395674962 Functional Loss SNV ICGC 33..33 33 LAML 2 - 113250 RMVar_ID_113250 Human_SNP_ID_845086526 m1A Human chr3 - 57692911 57692911 57692911 GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGGAGGCGCGCCAGAGGACGATGAAGAGGACGATGG GGCCGCGAGGCGCCGGCCCTTGTGGCGGCGGGGGGCGCGCCAGAGGACGATGAAGAGGACGATGG T C DENND6A Ensembl:ENSG00000174839 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:57692867..57693053 26863196 MeRIP-seq:(Medium) rs61737717 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,caecum adenocarcinoma,large_intestine adenocarcinoma 2 caecum,large intestine Human_RBP_ID_4758153,Human_RBP_ID_23026636 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219128 113251 RMVar_ID_113251 Human_SNP_ID_845126740 m1A Human chr3 + 184325076 184325076 184325076 AAGAGTCCCTTGAGTGCCTTTGTCGTCTGCTCACCACCATTGGCAAAGACCTGGACTTTGAAAAA AAGAGTCCCTTGAGTGCCTTTGTCGTCTGCTCGCCACCATTGGCAAAGACCTGGACTTTGAAAAA A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184325051..184325075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_11611,Human_RBP_ID_67261,Human_RBP_ID_1032265,Human_RBP_ID_1623390,Human_RBP_ID_1957530,Human_RBP_ID_4733625,Human_RBP_ID_7167791,Human_RBP_ID_8870203,Human_RBP_ID_9303127,Human_RBP_ID_9394360,Human_RBP_ID_17518787,Human_RBP_ID_23020943,Human_RBP_ID_26346360,Human_RBP_ID_27500265,Human_RBP_ID_27822791 Human_Splice_Rec_516699,Human_Splice_Rec_516763,Human_Splice_Rec_516821,Human_Splice_Rec_516883,Human_Splice_Rec_517011,Human_Splice_Rec_517071,Human_Splice_Rec_517105,Human_Splice_Rec_517141,Human_Splice_Rec_517197,Human_Splice_Rec_517293,Human_Splice_Rec_517355,Human_Splice_Rec_517417,Human_Splice_Rec_517485,Human_Splice_Rec_517567,Human_Splice_Rec_517623,Human_Splice_Rec_517689,Human_Splice_Rec_517719 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_54287,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374,RMVar_hsa_circ_309763,RMVar_hsa_circ_351209 113252 RMVar_ID_113252 Human_SNP_ID_845132764 m1A Human chr3 - 138535749 138535749 138535749 GAAGAATGAAAAAACAAAAAACAGTTAAGATGACTGGGTAAGAGGGTGAGAGAAGCACTGAGAGA GAAGAATGAAAAAACAAAAAACAGTTAAGATGGCTGGGTAAGAGGGTGAGAGAAGCACTGAGAGA T C CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:138535700..138535898 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_14645115 RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_38778,RMVar_hsa_circ_221679,RMVar_hsa_circ_68183,RMVar_hsa_circ_221677,RMVar_hsa_circ_10106,RMVar_hsa_circ_13379,RMVar_hsa_circ_317158,RMVar_hsa_circ_270865,RMVar_hsa_circ_278738,RMVar_hsa_circ_96880,RMVar_hsa_circ_221681,RMVar_hsa_circ_221680,RMVar_hsa_circ_71545,RMVar_hsa_circ_221678,RMVar_hsa_circ_30245 113253 RMVar_ID_113253 Human_SNP_ID_845138119 m1A Human chr3 - 127672476 127672476 127672476 GCCCACTCGGCCTGCGCCTCGGCTGCGCTCACAGGTGCGTGTCCTCCTCGAACACGTCCGAGTCC GCCCACTCGGCCTGCGCCTCGGCTGCGCTCACGGGTGCGTGTCCTCCTCGAACACGTCCGAGTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:127672426..127672675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113254 RMVar_ID_113254 Human_SNP_ID_845159166 m1A Human chr3 - 49025181 49025181 49025181 CGGCGCTTTGGTGTTCCGGTCATTGCTGATGGAGGAATCCAAAATGTGGGTCATATTGCGAAAGC CGGCGCTTTGGTGTTCCGGTCATTGCTGATGGGGGAATCCAAAATGTGGGTCATATTGCGAAAGC T C IMPDH2 Ensembl:ENSG00000178035 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_604014,Human_RBP_ID_1033589,Human_RBP_ID_1205745,Human_RBP_ID_1628391,Human_RBP_ID_1964479,Human_RBP_ID_8873017,Human_RBP_ID_17290445,Human_RBP_ID_18810264,Human_RBP_ID_22824079,Human_RBP_ID_27055040 Human_Splice_Rec_427121,Human_Splice_Rec_427140,Human_Splice_Rec_427141,Human_Splice_Rec_427166,Human_Splice_Rec_427167,Human_Splice_Rec_427177,Human_Splice_Rec_427183 Human_miRNA_ID_1954278,Human_miRNA_ID_3061247 RMVar_hsa_circ_93264,RMVar_hsa_circ_113558,RMVar_hsa_circ_127964,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218036,RMVar_hsa_circ_218037,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_300468 113255 RMVar_ID_113255 Human_SNP_ID_845161388 m1A Human chr3 - 45966662 45966662 45966662 CAAATGCAGCTCCGAGGAAGCACAGCTGGAGCACGCTGAGCTGCAAGAGCAGCTGCACCGGGCCA CAAATGCAGCTCCGAGGAAGCACAGCTGGAGCGCGCTGAGCTGCAAGAGCAGCTGCACCGGGCCA T C FYCO1 Ensembl:ENSG00000163820 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:45966613..45966783 26863196 MeRIP-seq:(Medium) rs754392183 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5530326,Human_RBP_ID_26346745 Human_miRNA_ID_206090,Human_miRNA_ID_1490259,Human_miRNA_ID_2757999 RMVar_hsa_circ_266342,RMVar_hsa_circ_113909,RMVar_hsa_circ_217458 113256 RMVar_ID_113256 Human_SNP_ID_845169283 m1A Human chr3 + 187745309 187745309 187745309 GCAAGAGCGGAAAAAAAAAGAATTAAAAGGTAAAATAATGATCATGAGCAGCGGCGGCGGCAGCG GCAAGAGCGGAAAAAAAAAGAATTAAAAGGTATAATAATGATCATGAGCAGCGGCGGCGGCAGCG A T AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:187745307..187745413 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 MALY,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_Splice_Rec_522554 113257 RMVar_ID_113257 Human_SNP_ID_845176696 m1A Human chr3 + 57597139 57597139 57597139 GTCGGGAGAAGAGGGAGGAGATAGTGAGGCCCATGGCGGTAGTGGCACTTGTGATGGGCAGAAGC GTCGGGAGAAGAGGGAGGAGATAGTGAGGCCCGTGGCGGTAGTGGCACTTGTGATGGGCAGAAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:57597090..57597350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 113258 RMVar_ID_113258 Human_SNP_ID_845212700 m1A Human chr3 - 179604589 179604589 179604589 GCTGCGGCCGGTTTGGCCCTTCTTTGTAGGAGAGTTTCATCCGCCCTGAAATCTTCCCGATCGTT GCTGCGGCCGGTTTGGCCCTTCTTTGTAGGAGGGTTTCATCCGCCCTGAAATCTTCCCGATCGTT T C MRPL47 Ensembl:ENSG00000136522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:179604490..179604603 26863196 MeRIP-seq:(Medium) rs1490249528 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_1622825,Human_RBP_ID_1956579,Human_RBP_ID_4757571,Human_RBP_ID_9334344,Human_RBP_ID_22092595,Human_RBP_ID_22509158,Human_RBP_ID_23213647,Human_RBP_ID_23987000 Human_Splice_Rec_509401,Human_Splice_Rec_509413,Human_Splice_Rec_509425 Human_miRNA_ID_2352952 RMVar_hsa_circ_126809,RMVar_hsa_circ_222936 113259 RMVar_ID_113259 Human_SNP_ID_845251191 m1A Human chr3 + 56633798 56633798 56633798 CTGCCTCTGCTGCTGGCACACACTGCTCCTCCACCTGACCTGTCAACACGTCATCCTCAGTGGTG CTGCCTCTGCTGCTGGCACACACTGCTCCTCCGCCTGACCTGTCAACACGTCATCCTCAGTGGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:56633750..56633836 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach RMVar_hsa_circ_219026 113260 RMVar_ID_113260 Human_SNP_ID_845277397 m1A Human chr3 - 52402676 52402676 52402676 GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTACAGATTGATGACCAGAGAAGGACCCACAACTACG GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTACGGATTGATGACCAGAGAAGGACCCACAACTACG T C BAP1 Ensembl:ENSG00000163930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402626..52402675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_437913,Human_Splice_Rec_437919,Human_Splice_Rec_437951,Human_Splice_Rec_437959,Human_Splice_Rec_437965 113261 RMVar_ID_113261 Human_SNP_ID_845283416 m1A Human chr3 + 63834064 63834064 63834064 TGCCAAAACTTTAAATATCTCAAGAGCATACCACATTTTAAACACATTATGGTCATGTAGCTATT TGCCAAAACTTTAAATATCTCAAGAGCATACCGCATTTTAAACACATTATGGTCATGTAGCTATT A G C3orf49 Ensembl:ENSG00000163632 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:63833972..63834118 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 113262 RMVar_ID_113262 Human_SNP_ID_845290498 m1A Human chr3 + 158097997 158097997 158097997 GCGCGGAGGGCGTGCAGGCTGAGTGCCGCGGGACAGGCGCGACATTGGTGCTGGCGTTGGCGTCA GCGCGGAGGGCGTGCAGGCTGAGTGCCGCGGGGCAGGCGCGACATTGGTGCTGGCGTTGGCGTCA A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:158097906..158098055 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113263 RMVar_ID_113263 Human_SNP_ID_845356056 m1A Human chr3 - 49101691 49101691 49101691 TTATTCTGGTCCTGGCAGGTGAGAACTACAAGACCCCAGGCTATGTGGTCACTCCACACACCATG TTATTCTGGTCCTGGCAGGTGAGAACTACAAGGCCCCAGGCTATGTGGTCACTCCACACACCATG T C QARS1 Ensembl:ENSG00000172053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49101601..49101725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_8574781,Human_RBP_ID_17291410,Human_RBP_ID_22455442,Human_RBP_ID_26823871 Human_Splice_Rec_427382,Human_Splice_Rec_427383,Human_Splice_Rec_427434,Human_Splice_Rec_427435,Human_Splice_Rec_427480,Human_Splice_Rec_427481,Human_Splice_Rec_427544,Human_Splice_Rec_427545,Human_Splice_Rec_427594,Human_Splice_Rec_427595,Human_Splice_Rec_427668,Human_Splice_Rec_427669,Human_Splice_Rec_427722,Human_Splice_Rec_427723,Human_Splice_Rec_427798,Human_Splice_Rec_427799,Human_Splice_Rec_427838,Human_Splice_Rec_427839,Human_Splice_Rec_427860,Human_Splice_Rec_427861,Human_Splice_Rec_427878,Human_Splice_Rec_427879,Human_Splice_Rec_427934,Human_Splice_Rec_427935,Human_Splice_Rec_427952,Human_Splice_Rec_427953,Human_Splice_Rec_427966,Human_Splice_Rec_427980,Human_Splice_Rec_427996 Human_miRNA_ID_2157018 RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_80291,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_218065,RMVar_hsa_circ_25559,RMVar_hsa_circ_78406,RMVar_hsa_circ_218068 113264 RMVar_ID_113264 Human_SNP_ID_845385736 m1A Human chr3 + 158732345 158732345 158732345 CCACCGGGGCGAGCAACAGCAGCAGCGCGAGCAGCGGGGCGGTGGGGCGCGGGCCCCTGGGCCCG CCACCGGGGCGAGCAACAGCAGCAGCGCGAGCCGCGGGGCGGTGGGGCGCGGGCCCCTGGGCCCG A C MFSD1,AC080013.1 Ensembl:ENSG00000118855,Ensembl:ENSG00000240207 Protein coding,lincRNA 5'UTR,exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:158732297..158732528 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - RMVar_hsa_circ_222378 113265 RMVar_ID_113265 Human_SNP_ID_845392919 m1A Human chr3 + 50299317 50299317 50299317 TCGGACTCCTCGGTCCGACAACGTTGGCCCCCAGCGGTGCGGCGGATGTTCTGCAGCCGTCGCGT TCGGACTCCTCGGTCCGACAACGTTGGCCCCCGGCGGTGCGGCGGATGTTCTGCAGCCGTCGCGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50299026..50299400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach 113266 RMVar_ID_113266 Human_SNP_ID_845415633 m1A Human chr3 + 12839528 12839528 12839528 CTGTTGTCAATGCCTCTGGGTTTCCGCCAGTTACGCTGAAGGAAATAATACACAGGTGGGTTAGC CTGTTGTCAATGCCTCTGGGTTTCCGCCAGTTGCGCTGAAGGAAATAATACACAGGTGGGTTAGC A G CAND2 Ensembl:ENSG00000144712 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12839400..12839580 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach 113267 RMVar_ID_113267 Human_SNP_ID_845418065 m1A Human chr3 - 128052477 128052477 128052477 TGCTCCGCGTGAGGCGACGCTGCCCGCGGCCCAGCGCGTTCCACTGCACAGCAGCTCCGCCGAGA TGCTCCGCGTGAGGCGACGCTGCCCGCGGCCCGGCGCGTTCCACTGCACAGCAGCTCCGCCGAGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:128052426..128052525;chr3:128052426..128052500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - RMVar_hsa_circ_221024,RMVar_hsa_circ_221023 113268 RMVar_ID_113268 Human_SNP_ID_845443936 m1A Human chr3 - 64023441 64023441 64023441 CGCAGCCGGTCGTAACCAAGTTGTGTCCTGTCAGCCGCTGTCCCCTTCGCCGCGATGCCGCTGGA CGCAGCCGGTCGTAACCAAGTTGTGTCCTGTCTGCCGCTGTCCCCTTCGCCGCGATGCCGCTGGA T A PSMD6 Ensembl:ENSG00000163636 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:64023325..64023475 26863196 MeRIP-seq:(Medium) rs143451892 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_RBP_ID_158279,Human_RBP_ID_9333777,Human_RBP_ID_9393815,Human_RBP_ID_14926762,Human_RBP_ID_22091791,Human_RBP_ID_23026743,Human_RBP_ID_24016319,Human_RBP_ID_26347031 Human_Splice_Rec_449061,Human_Splice_Rec_449087 113269 RMVar_ID_113269 Human_SNP_ID_845444040 m1A Human chr3 - 49017723 49017723 49017723 GAGCCACGCCCTTGAAGAACTTACCTCTGCTAATGACGGGAGGACACTGTCCCCTGGCATCCTAG GAGCCACGCCCTTGAAGAACTTACCTCTGCTAGTGACGGGAGGACACTGTCCCCTGGCATCCTAG T C DALRD3 Ensembl:ENSG00000178149 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49017674..49017802 26863196 MeRIP-seq:(Medium) rs761345101 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,UCEC,endometrium endometrioid_carcinoma 14 uterus,pancreas Human_RBP_ID_246912 RMVar_hsa_circ_218030,RMVar_hsa_circ_86112 113270 RMVar_ID_113270 Human_SNP_ID_845447371 m1A Human chr3 - 14944928 14944928 14944928 TGGCTCATGCCTGTAATCCCAGCATTTTGGGAAGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG TGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1142981 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_592374,Human_RBP_ID_5654819,Human_RBP_ID_26510847 RMVar_hsa_circ_216093,RMVar_hsa_circ_112835 113271 RMVar_ID_113271 Human_SNP_ID_845452474 m1A Human chr3 - 134361652 134361652 134361652 GGGCAGCTCGAGCCGAAGAGGAGCTGCGCAAGAAGCAGGCCTATGTGGAGAAAGTGGAGCGGCTG GGGCAGCTCGAGCCGAAGAGGAGCTGCGCAAGGAGCAGGCCTATGTGGAGAAAGTGGAGCGGCTG T C AMOTL2 Ensembl:ENSG00000114019 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:134361601..134361675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 4 oesophagus RMVar_hsa_circ_17488,RMVar_hsa_circ_99655,RMVar_hsa_circ_51792,RMVar_hsa_circ_221492,RMVar_hsa_circ_109867,RMVar_hsa_circ_221494,RMVar_hsa_circ_221495 113272 RMVar_ID_113272 Human_SNP_ID_845542485 m1A Human chr3 + 153162328 153162328 153162328 GCGCGTCCCGGCCCGACGCGCAATTAGCAGCCACCTCCGCAGCCCGCCGCCACCGCCTCCCTGCC GCGCGTCCCGGCCCGACGCGCAATTAGCAGCCCCCTCCGCAGCCCGCCGCCACCGCCTCCCTGCC A C RAP2B Ensembl:ENSG00000181467 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:153162277..153162435 26863196 MeRIP-seq:(Medium) rs1025578704 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_310432,Human_RBP_ID_4757518 113273 RMVar_ID_113273 Human_SNP_ID_845574974 m1A Human chr3 - 187729392 187729392 187729392 TCTGGTTAGTCCACAGAGCCCCCAGAAATCTGACTGCCAGCCCAACTCGCCCACAGAGTCCTGCA TCTGGTTAGTCCACAGAGCCCCCAGAAATCTGGCTGCCAGCCCAACTCGCCCACAGAGTCCTGCA T C BCL6 Ensembl:ENSG00000113916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:187729278..187729556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_miRNA_ID_1013278,Human_miRNA_ID_1295279,Human_miRNA_ID_1299236 RMVar_hsa_circ_365430,RMVar_hsa_circ_57705 113274 RMVar_ID_113274 Human_SNP_ID_845582459 m1A Human chr3 + 52435645 52435645 52435645 TCCACCTCCCGGGGCGTCCGATTGTGCTCGGCATGCACCCGGCTCTTCATCTTCTTGCCTAGCTC TCCACCTCCCGGGGCGTCCGATTGTGCTCGGCGTGCACCCGGCTCTTCATCTTCTTGCCTAGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:52435638..52435722 26863196 MeRIP-seq:(Medium) rs1298477697 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 113275 RMVar_ID_113275 Human_SNP_ID_845597710 m1A Human chr3 + 195523784 195523784 195523784 GATACTTTGGCTCCAAGCCTTCAGCTGCAGCTAATCTATGCAACAATCATGTACAAAGAAATTAA GATACTTTGGCTCCAAGCCTTCAGCTGCAGCTGATCTATGCAACAATCATGTACAAAGAAATTAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:195523743..195523820 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 113276 RMVar_ID_113276 Human_SNP_ID_845656475 m1A Human chr3 + 129161024 129161024 129161024 CCGTCCTGGAGCCCCGCGGCCCCTGTCCAAGAAACTCCACAGGCCCAGAAGACGCCGACGCTCAC CCGTCCTGGAGCCCCGCGGCCCCTGTCCAAGATACTCCACAGGCCCAGAAGACGCCGACGCTCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129158556..129161049 26863196 MeRIP-seq:(Medium) rs1341052177 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113277 RMVar_ID_113277 Human_SNP_ID_845676114 m1A Human chr3 - 37862280 37862280 37862280 CCCCCAGCCCGCGGCCGCCTGCGCCCCTCCTCACCTTTCTCGCCCGCGCCCGGCAACCGGCCCTC CCCCCAGCCCGCGGCCGCCTGCGCCCCTCCTCCCCTTTCTCGCCCGCGCCCGGCAACCGGCCCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:37862187..37862490;chr3:37862180..37862494 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113278 RMVar_ID_113278 Human_SNP_ID_845717392 m1A Human chr3 - 133933478 133933478 133933478 GCCAACGAAGGAGGTCATTCATCAACAAATATATTTATTGGAGACCGACTTTGTGCAAAGCAATG GCCAACGAAGGAGGTCATTCATCAACAAATATGTTTATTGGAGACCGACTTTGTGCAAAGCAATG T C SLCO2A1 Ensembl:ENSG00000174640 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1131598 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_13147,GWAS_ID_13148,GWAS_ID_13149 113279 RMVar_ID_113279 Human_SNP_ID_845757003 m1A Human chr3 - 52403205 52403204 52403205 CCCAGTGGAGAAGGAGGTCGTGGAAGCCACGGACAGCAGAGAGAAGACGGGGATGGTGAGGCCTG CCCAGTGGAGAAGGAGGTCGTGGAAGCCACGG_CAGCAGAGAGAAGACGGGGATGGTGAGGCCTG GT G BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr3:52403119..52403272;chr3:52403126..52403300 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 CHOL 1 - Human_Splice_Rec_437908,Human_Splice_Rec_437909,Human_Splice_Rec_437946,Human_Splice_Rec_437947,Human_Splice_Rec_437954,Human_Splice_Rec_437955,Human_Splice_Rec_437962 113280 RMVar_ID_113280 Human_SNP_ID_845805585 m1A Human chr3 - 142005486 142005486 142005486 GTTTCCAATACCAACTCACCTACAAAGATTTTACCAAAAACCTTAGGACCAATAAATGTGAATGT GTTTCCAATACCAACTCACCTACAAAGATTTTGCCAAAAACCTTAGGACCAATAAATGTGAATGT T C TFDP2 Ensembl:ENSG00000114126 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7627056 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 25 uterus,head and neck,large intestine Human_RBP_ID_17291574,Human_RBP_ID_17401858 Human_Splice_Rec_491134,Human_Splice_Rec_491135,Human_Splice_Rec_491172,Human_Splice_Rec_491173,Human_Splice_Rec_491206,Human_Splice_Rec_491207,Human_Splice_Rec_491230,Human_Splice_Rec_491231,Human_Splice_Rec_491249,Human_Splice_Rec_491270,Human_Splice_Rec_491271,Human_Splice_Rec_491296,Human_Splice_Rec_491297,Human_Splice_Rec_491324,Human_Splice_Rec_491325,Human_Splice_Rec_491348,Human_Splice_Rec_491349,Human_Splice_Rec_491352,Human_Splice_Rec_491353,Human_Splice_Rec_491362,Human_Splice_Rec_491363,Human_Splice_Rec_491368,Human_Splice_Rec_491369,Human_Splice_Rec_491374,Human_Splice_Rec_491375,Human_Splice_Rec_491382,Human_Splice_Rec_491383,Human_Splice_Rec_491396,Human_Splice_Rec_491397 GWAS_ID_14542,GWAS_ID_14543,GWAS_ID_14544,GWAS_ID_14545,GWAS_ID_14546,GWAS_ID_14547,GWAS_ID_14548,GWAS_ID_14549,GWAS_ID_14550,GWAS_ID_14551,GWAS_ID_14552,GWAS_ID_14553 RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_294302,RMVar_hsa_circ_17243,RMVar_hsa_circ_73369,RMVar_hsa_circ_221860,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_316443,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_40191,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_290615,RMVar_hsa_circ_348867,RMVar_hsa_circ_221869,RMVar_hsa_circ_324638,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872 113281 RMVar_ID_113281 Human_SNP_ID_845813126 m1A Human chr3 + 47847808 47847808 47847808 ACCAGTGCACTCCAACATCCCCATGATGGATCAGAAGGCCATATTCCAGCAGCCTCCAGTTGGGG ACCAGTGCACTCCAACATCCCCATGATGGATCTGAAGGCCATATTCCAGCAGCCTCCAGTTGGGG A T DHX30 Ensembl:ENSG00000132153 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:47847801..47847950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_1963981 Human_Splice_Rec_423042,Human_Splice_Rec_423100,Human_Splice_Rec_423144,Human_Splice_Rec_423182,Human_Splice_Rec_423218,Human_Splice_Rec_423254 RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_124152,RMVar_hsa_circ_100897,RMVar_hsa_circ_217774,RMVar_hsa_circ_115410,RMVar_hsa_circ_121322,RMVar_hsa_circ_217775,RMVar_hsa_circ_217776,RMVar_hsa_circ_217777,RMVar_hsa_circ_86193,RMVar_hsa_circ_217778 113282 RMVar_ID_113282 Human_SNP_ID_845891574 m1A Human chr3 + 197782055 197782053 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTT__AAAAAAAAAACGTATAAAATAATGCCCTGAAA TTA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA,ICGC 32..33 33 COAD,COCA 3 - Human_RBP_ID_69843,Human_RBP_ID_598524 113283 RMVar_ID_113283 Human_SNP_ID_845918376 m1A Human chr3 + 50257575 50257575 50257575 GTTTGAGGACCTGAATAAGCGCAAAGACACCAAGGAGATCTACACGCACTTCACGTGCGCCACCG GTTTGAGGACCTGAATAAGCGCAAAGACACCATGGAGATCTACACGCACTTCACGTGCGCCACCG A T GNAI2 Ensembl:ENSG00000114353 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50257526..50257754 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_18194603,Human_RBP_ID_26823890 Human_Splice_Rec_432738,Human_Splice_Rec_432756,Human_Splice_Rec_432772,Human_Splice_Rec_432788,Human_Splice_Rec_432804,Human_Splice_Rec_432820,Human_Splice_Rec_432834,Human_Splice_Rec_432850,Human_Splice_Rec_432862,Human_Splice_Rec_432872 Human_miRNA_ID_1112247 RMVar_hsa_circ_327248,RMVar_hsa_circ_218411,RMVar_hsa_circ_354790,RMVar_hsa_circ_354757 113284 RMVar_ID_113284 Human_SNP_ID_845929264 m1A Human chr3 + 48433869 48433869 48433869 ACAAGCCCTCGAGCCACCATGAACACTTTCTCAGCCTGCAAAGAGAAAACCGGAGGCCATCTGCA ACAAGCCCTCGAGCCACCATGAACACTTTCTCGGCCTGCAAAGAGAAAACCGGAGGCCATCTGCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:48433726..48433929 26863196 MeRIP-seq:(Medium) rs1268898646 Functional Loss SNV ICGC 33..33 33 SARC 1 - 113285 RMVar_ID_113285 Human_SNP_ID_845929931 m1A Human chr3 - 124859335 124859335 124859335 TAGAGAGCCCAGCCAGCAGCTTCCATGTCCTGAGGAGCCTGCCCCTCAGCAGCAAGGGTTCGGGC TAGAGAGCCCAGCCAGCAGCTTCCATGTCCTGGGGAGCCTGCCCCTCAGCAGCAAGGGTTCGGGC T C ITGB5 Ensembl:ENSG00000082781 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:124859285..124859386 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 WT 1 - Human_RBP_ID_4756671 Human_Splice_Rec_476369,Human_Splice_Rec_476449,Human_Splice_Rec_476461,Human_Splice_Rec_476469,Human_Splice_Rec_476475 Human_miRNA_ID_2389654,Human_miRNA_ID_2590877,Human_miRNA_ID_2625851,Human_miRNA_ID_2746674 RMVar_hsa_circ_16955,RMVar_hsa_circ_364396,RMVar_hsa_circ_365149,RMVar_hsa_circ_220838,RMVar_hsa_circ_357345,RMVar_hsa_circ_364220,RMVar_hsa_circ_220840,RMVar_hsa_circ_363896,RMVar_hsa_circ_353290,RMVar_hsa_circ_357724,RMVar_hsa_circ_6983,RMVar_hsa_circ_220841,RMVar_hsa_circ_107896,RMVar_hsa_circ_220844,RMVar_hsa_circ_88801,RMVar_hsa_circ_322744,RMVar_hsa_circ_293902,RMVar_hsa_circ_220845,RMVar_hsa_circ_69825,RMVar_hsa_circ_285095,RMVar_hsa_circ_353924 113286 RMVar_ID_113286 Human_SNP_ID_845939514 m1A Human chr3 - 9902958 9902958 9902958 GGTCGATGACTATGAGGAGGAGAGGCAGGAGCAGGGCTGCCAGTCTGGAGCTCCCCATGGGCTTC GGTCGATGACTATGAGGAGGAGAGGCAGGAGCGGGGCTGCCAGTCTGGAGCTCCCCATGGGCTTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9902945..9903028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 113287 RMVar_ID_113287 Human_SNP_ID_845943437 m1A Human chr3 - 48473053 48473053 48473053 GAGTGGCCCACGATGGGAAGAGGGGAAAGCCCAGGGGTACAGGAGGCCTCTGGGTGAAGGCAGAG GAGTGGCCCACGATGGGAAGAGGGGAAAGCCCCGGGGTACAGGAGGCCTCTGGGTGAAGGCAGAG T G SHISA5 Ensembl:ENSG00000164054 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:48469694..48473116;chr3:48469726..48473125;chr3:48472967..48473100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_247662,Human_RBP_ID_783808,Human_RBP_ID_4756435,Human_RBP_ID_5120540,Human_RBP_ID_17291380,Human_RBP_ID_18194564,Human_RBP_ID_18446679,Human_RBP_ID_22455801 Human_Splice_Rec_424563,Human_Splice_Rec_424567,Human_Splice_Rec_424615,Human_Splice_Rec_424617 RMVar_hsa_circ_351627 113288 RMVar_ID_113288 Human_SNP_ID_845959068 m1A Human chr3 + 55488156 55488156 55488156 GGGTCCGAGGGGCGGGAGAGCGGGCCGGCGGGAGGCGGGCGGTCCCGGGCACAACGGCGGCGGCG GGGTCCGAGGGGCGGGAGAGCGGGCCGGCGGGTGGCGGGCGGTCCCGGGCACAACGGCGGCGGCG A T WNT5A-AS1 Ensembl:ENSG00000244586 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:55488019..55488274 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113289 RMVar_ID_113289 Human_SNP_ID_845974856 m1A Human chr3 - 57597149 57597149 57597149 AACCCCTTCTGCTTCTGCCCATCACAAGTGCCACTACCGCCATGGGCCTCACTATCTCCTCCCTC AACCCCTTCTGCTTCTGCCCATCACAAGTGCCCCTACCGCCATGGGCCTCACTATCTCCTCCCTC T G ARF4 Ensembl:ENSG00000168374 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:57597126..57597150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas Human_RBP_ID_68779,Human_RBP_ID_5447806,Human_RBP_ID_17404661,Human_RBP_ID_20930191,Human_RBP_ID_24013830 Human_Splice_Rec_444975,Human_Splice_Rec_444985,Human_Splice_Rec_444993,Human_Splice_Rec_444999,Human_Splice_Rec_445009,Human_Splice_Rec_445016,Human_Splice_Rec_445017,Human_Splice_Rec_445025,Human_Splice_Rec_445029,Human_Splice_Rec_445032 RMVar_hsa_circ_76920,RMVar_hsa_circ_219107 113290 RMVar_ID_113290 Human_SNP_ID_845993050 m1A Human chr3 - 129316064 129316064 129316064 CCCAACCCTCGCTCCGGCCCGGCCCGGCCCCCACCCCAGCCCTGCCGCCCGGCCCCAGGCCCGGC CCCAACCCTCGCTCCGGCCCGGCCCGGCCCCCCCCCCAGCCCTGCCGCCCGGCCCCAGGCCCGGC T G H1-10 Ensembl:ENSG00000184897 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:129315864..129316275 26863410 MeRIP-seq:(Medium) rs932501128 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_248637,Human_RBP_ID_4760914,Human_RBP_ID_5505476,Human_RBP_ID_22456170,Human_RBP_ID_22533870 113291 RMVar_ID_113291 Human_SNP_ID_846055439 m1A Human chr3 - 46681327 46681327 46681327 GCACGGATTTGGGGTCCTTGAGAGTGGTCCGCAGGCCCCCCAGCCCTTCAGGTACACGGGCCACT GCACGGATTTGGGGTCCTTGAGAGTGGTCCGCCGGCCCCCCAGCCCTTCAGGTACACGGGCCACT T G ALS2CL Ensembl:ENSG00000178038 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:46681280..46681362 26863196 MeRIP-seq:(Medium) rs369892563 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_Splice_Rec_420562,Human_Splice_Rec_420563,Human_Splice_Rec_420628,Human_Splice_Rec_420629,Human_Splice_Rec_420678,Human_Splice_Rec_420679,Human_Splice_Rec_420748,Human_Splice_Rec_420790,Human_Splice_Rec_420826,Human_Splice_Rec_420827 RMVar_hsa_circ_57807,RMVar_hsa_circ_116435,RMVar_hsa_circ_217465 113292 RMVar_ID_113292 Human_SNP_ID_846063666 m1A Human chr3 - 31981021 31981021 31981021 CGGTCGGCGGCGGCCGGGCTCGGCGGCGGGGGAAGCCGCAGCAGCCCGGGCTCTGTGGCCGCTAG CGGTCGGCGGCGGCCGGGCTCGGCGGCGGGGGGAGCCGCAGCAGCCCGGGCTCTGTGGCCGCTAG T C OSBPL10 Ensembl:ENSG00000144645 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:31980970..31981264 26863196 MeRIP-seq:(Medium) rs1050361341 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 4 haematopoietic and lymphoid tissue Human_RBP_ID_4756359,Human_RBP_ID_9354375 113293 RMVar_ID_113293 Human_SNP_ID_846097650 m1A Human chr3 - 50318057 50318057 50318057 ACAAGGGCTCTCTTAGGCATGTAGGACCCTGCAGGGGGTGGACAAACTGGAGTCTGGAGTGGGCA ACAAGGGCTCTCTTAGGCATGTAGGACCCTGCGGGGGGTGGACAAACTGGAGTCTGGAGTGGGCA T C HYAL2 Ensembl:ENSG00000068001 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:50317839..50318339 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_604677,Human_RBP_ID_14877449,Human_RBP_ID_17661128,Human_RBP_ID_27320334,Human_RBP_ID_27503350 Human_miRNA_ID_960817,Human_miRNA_ID_1335162 113294 RMVar_ID_113294 Human_SNP_ID_846120343 m1A Human chr3 + 50318189 50318189 50318189 GCCAGAGCCAGCAGACTGGTGAGGTGGGACCCAGCCCAGGCCTCGCTGGCACCTCCAGCTGCCTG GCCAGAGCCAGCAGACTGGTGAGGTGGGACCCGGCCCAGGCCTCGCTGGCACCTCCAGCTGCCTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:50318139..50318339 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 4 stomach RMVar_hsa_circ_218424 113295 RMVar_ID_113295 Human_SNP_ID_846133647 m1A Human chr3 + 48410512 48410512 48410512 CGCCTCCACAGACCCTGGACCTCAGAAGTGACATCCTCGTCAGAAAGAATGAGGTGCCCGGCCAC CGCCTCCACAGACCCTGGACCTCAGAAGTGACTTCCTCGTCAGAAAGAATGAGGTGCCCGGCCAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:48410464..48410615 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 3 haematopoietic and lymphoid tissue 113296 RMVar_ID_113296 Human_SNP_ID_846140812 m1A Human chr3 - 40457377 40457377 40457377 GAGCGGCATGGTCGACGGCCCCGGAGCCCGCAACAGTAAGACTCACCATGTTGGCGGCGTTAGGC GAGCGGCATGGTCGACGGCCCCGGAGCCCGCAGCAGTAAGACTCACCATGTTGGCGGCGTTAGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:40457375..40457512 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113297 RMVar_ID_113297 Human_SNP_ID_846152763 m1A Human chr3 + 56613652 56613652 56613652 GCAGGAAGAAACAACTGGAGGAAGAGCAAAGAAAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTA GCAGGAAGAAACAACTGGAGGAAGAGCAAAGAGAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTA A G CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:56613594..56613705 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_247921,Human_RBP_ID_935518,Human_RBP_ID_22284759,Human_RBP_ID_24547275,Human_RBP_ID_26348196 Human_Splice_Rec_443532,Human_Splice_Rec_443533,Human_Splice_Rec_443574,Human_Splice_Rec_443575,Human_Splice_Rec_443608,Human_Splice_Rec_443609,Human_Splice_Rec_443674,Human_Splice_Rec_443675,Human_Splice_Rec_443718,Human_Splice_Rec_443719,Human_Splice_Rec_443760,Human_Splice_Rec_443761,Human_Splice_Rec_443786,Human_Splice_Rec_443787 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_353235,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_59971,RMVar_hsa_circ_367613 113298 RMVar_ID_113298 Human_SNP_ID_846180566 m1A Human chr3 + 184322843 184322843 184322843 TTCCTTGCAGATCAGTGGAAGCCTCTAAACCTAGAGGAGAAAAAACGTTACGACCGTGAGTTCCT TTCCTTGCAGATCAGTGGAAGCCTCTAAACCTGGAGGAGAAAAAACGTTACGACCGTGAGTTCCT A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:184322826..184322850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 13 prostate Human_RBP_ID_1623364,Human_RBP_ID_1957513,Human_RBP_ID_8870167,Human_RBP_ID_9394345,Human_RBP_ID_22092883,Human_RBP_ID_23989287 Human_Splice_Rec_516688,Human_Splice_Rec_516752,Human_Splice_Rec_516810,Human_Splice_Rec_516872,Human_Splice_Rec_516934,Human_Splice_Rec_516966,Human_Splice_Rec_517000,Human_Splice_Rec_517060,Human_Splice_Rec_517094,Human_Splice_Rec_517130,Human_Splice_Rec_517186,Human_Splice_Rec_517282,Human_Splice_Rec_517344,Human_Splice_Rec_517406,Human_Splice_Rec_517474,Human_Splice_Rec_517528,Human_Splice_Rec_517556,Human_Splice_Rec_517612,Human_Splice_Rec_517678 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374 113299 RMVar_ID_113299 Human_SNP_ID_846189755 m1A Human chr3 - 128813449 128813449 128813449 GAAGGCCTACGTGTGTTCTTGGTTTGTGAAGGACTCTGTGCTCAACTCTCACTGCCCCCTCAGCA GAAGGCCTACGTGTGTTCTTGGTTTGTGAAGGGCTCTGTGCTCAACTCTCACTGCCCCCTCAGCA T C lnc-KIAA1257-7 RNACentral:URS00008BF864 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:128813399..128813747 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - 113300 RMVar_ID_113300 Human_SNP_ID_846209191 m1A Human chr3 + 149970834 149970834 149970834 CCTGGCAGCAGCCATCGCACATCAGGTTATCCACGTAGCTCTGCCAACCGGCCATCTTCGAGCCC CCTGGCAGCAGCCATCGCACATCAGGTTATCCTCGTAGCTCTGCCAACCGGCCATCTTCGAGCCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:149970515..149970950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 10 lung 113301 RMVar_ID_113301 Human_SNP_ID_846249058 m1A Human chr3 + 48501252 48501252 48501252 ACCACAGCAGAAATCTGGACAGGACTCGGGGAAGAGGCTGAGTCCACGGGAAGCCATACACACCT ACCACAGCAGAAATCTGGACAGGACTCGGGGACGAGGCTGAGTCCACGGGAAGCCATACACACCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48501201..48502359 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 5 stomach 113302 RMVar_ID_113302 Human_SNP_ID_846251322 m1A Human chr3 - 48587929 48587929 48587929 CCCACCCTCACGCCTGCCCCAGGTGGCCAGGAACAGTCCCGGGTCCTGGGGCCCGAGCTCAGCAG CCCACCCTCACGCCTGCCCCAGGTGGCCAGGAGCAGTCCCGGGTCCTGGGGCCCGAGCTCAGCAG T C COL7A1 Ensembl:ENSG00000114270 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48587796..48587955 26863196 MeRIP-seq:(Medium) rs201566458 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_Splice_Rec_425110 RMVar_hsa_circ_110617,RMVar_hsa_circ_217874,RMVar_hsa_circ_116423,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_121184,RMVar_hsa_circ_111079,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_125520,RMVar_hsa_circ_217896,RMVar_hsa_circ_217898,RMVar_hsa_circ_86729,RMVar_hsa_circ_217897,RMVar_hsa_circ_94323,RMVar_hsa_circ_84641,RMVar_hsa_circ_103797,RMVar_hsa_circ_217903,RMVar_hsa_circ_86491,RMVar_hsa_circ_217905,RMVar_hsa_circ_217906,RMVar_hsa_circ_217904,RMVar_hsa_circ_46358,RMVar_hsa_circ_111922,RMVar_hsa_circ_119042,RMVar_hsa_circ_217910,RMVar_hsa_circ_83340,RMVar_hsa_circ_217911,RMVar_hsa_circ_217909 113303 RMVar_ID_113303 Human_SNP_ID_846252193 m1A Human chr3 + 12539189 12539189 12539189 GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCAATGCTGCGATCTTGGATCACTGCAACCTCTGC GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCGATGCTGCGATCTTGGATCACTGCAACCTCTGC A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs113368836 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_9131581 Human_Splice_Rec_395778,Human_Splice_Rec_395808 GWAS_ID_110,GWAS_ID_111,GWAS_ID_112,GWAS_ID_113 RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 113304 RMVar_ID_113304 Human_SNP_ID_846257237 m1A Human chr3 + 197782055 197782054 197782056 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTTT__AAAAAAAAACGTATAAAATAATGCCCTGAAA TAA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 33..34 33 CHOL 1 - Human_RBP_ID_69843,Human_RBP_ID_598524 113305 RMVar_ID_113305 Human_SNP_ID_846266280 m1A Human chr3 - 48469502 48469502 48469502 CCCCTTATCCTCAGCCTCCAAGTGTGCCGCCCAGCTACCCTGGACCAAGCTACCAGGGCTACCAC CCCCTTATCCTCAGCCTCCAAGTGTGCCGCCCTGCTACCCTGGACCAAGCTACCAGGGCTACCAC T A SHISA5 Ensembl:ENSG00000164054 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr3:48469401..48469602;chr3:48469401..48469633;chr3:48469451..48469603 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver Human_RBP_ID_603503,Human_RBP_ID_783807,Human_RBP_ID_17292377,Human_RBP_ID_17404606,Human_RBP_ID_17521402,Human_RBP_ID_17661094,Human_RBP_ID_18953526,Human_RBP_ID_24006614,Human_RBP_ID_26511081 Human_Splice_Rec_424536,Human_Splice_Rec_424546,Human_Splice_Rec_424556,Human_Splice_Rec_424560,Human_Splice_Rec_424566,Human_Splice_Rec_424570,Human_Splice_Rec_424576,Human_Splice_Rec_424580,Human_Splice_Rec_424592,Human_Splice_Rec_424602,Human_Splice_Rec_424612,Human_Splice_Rec_424624,Human_Splice_Rec_424634 Human_miRNA_ID_246368,Human_miRNA_ID_248883,Human_miRNA_ID_2033731,Human_miRNA_ID_2035035 RMVar_hsa_circ_326333,RMVar_hsa_circ_351627 113306 RMVar_ID_113306 Human_SNP_ID_846302657 m1A Human chr3 - 58156062 58156062 58156062 ATGCTTCCTTGCATCTCACCTGAAGGCTCATAACAGTGAGGCGGCGGGCGTCGTCGGAGGGTGCG ATGCTTCCTTGCATCTCACCTGAAGGCTCATACCAGTGAGGCGGCGGGCGTCGTCGGAGGGTGCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:58156011..58156116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - RMVar_hsa_circ_219259 113307 RMVar_ID_113307 Human_SNP_ID_846302761 m1A Human chr3 + 147393857 147393857 147393857 CGGTTGCTGGCCCGCGCCTCCCTCCCCGAGGCACCATTGTTCCGGGATCGCTGTGACCGCCACAA CGGTTGCTGGCCCGCGCCTCCCTCCCCGAGGCGCCATTGTTCCGGGATCGCTGTGACCGCCACAA A G ZIC1 Ensembl:ENSG00000152977 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:147393719..147393919 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 12 prostate Human_Splice_Rec_494217,Human_Splice_Rec_494219 113308 RMVar_ID_113308 Human_SNP_ID_846316615 m1A Human chr3 + 49131664 49131664 49131664 GCCCCACAGTCATAGGAGAAATATCGGTACACATGCCAGGTGCGGCCAAAGTCTGCTGAGCGTTC GCCCCACAGTCATAGGAGAAATATCGGTACACGTGCCAGGTGCGGCCAAAGTCTGCTGAGCGTTC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49131526..49131675 32194978 MeRIP-seq:(Medium) rs1331458305 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus 113309 RMVar_ID_113309 Human_SNP_ID_846335033 m1A Human chr3 - 121831119 121831119 121831119 CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCATGTCCTCCCTGCCTGTGATATCCAGGAAATTC CTGTGAAGTATGGGAAGGGGCACAGAGCTTCCGTGTCCTCCCTGCCTGTGATATCCAGGAAATTC T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7612301 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,liver hepatocellular_carcinoma 3 liver GWAS_ID_13126,GWAS_ID_13127,GWAS_ID_13128 113310 RMVar_ID_113310 Human_SNP_ID_846356741 m1A Human chr3 + 184170197 184170197 184170197 TCCCGGAGCTGGGCTACAGCTACGGCGGGGGCAGCGCCAGCAGTCAGCACAGCGAAGGTAAGGTA TCCCGGAGCTGGGCTACAGCTACGGCGGGGGCGGCGCCAGCAGTCAGCACAGCGAAGGTAAGGTA A G DVL3 Ensembl:ENSG00000161202 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184170150..184170221 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_3964433 Human_Splice_Rec_515393,Human_Splice_Rec_515437,Human_Splice_Rec_515483,Human_Splice_Rec_515517 113311 RMVar_ID_113311 Human_SNP_ID_846382362 m1A Human chr3 - 196318115 196318115 196318115 CACGTCCATCGGAGTGTCCTTCTCGGTGGGCGACGGGGTGCCTGAGGCTGAGAAGAACGCAGGGG CACGTCCATCGGAGTGTCCTTCTCGGTGGGCGCCGGGGTGCCTGAGGCTGAGAAGAACGCAGGGG T G TM4SF19-TCTEX1D2,TCTEX1D2,AC069257.4 Ensembl:ENSG00000273331,Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding,Protein coding intron,CDS,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:196318076..196318285 26863196 MeRIP-seq:(Medium) rs1446527339 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_597908,Human_RBP_ID_26347623 Human_Splice_Rec_530449 113312 RMVar_ID_113312 Human_SNP_ID_846416555 m1A Human chr3 - 170419128 170419128 170419128 CCACCCAGTCATTGGTGGAGGTGGTCACGATGACCCCGATCCAGCCCACGAAGCTCGTGACGAAG CCACCCAGTCATTGGTGGAGGTGGTCACGATGGCCCCGATCCAGCCCACGAAGCTCGTGACGAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:170418914..170419300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113313 RMVar_ID_113313 Human_SNP_ID_846434866 m1A Human chr3 - 195658143 195658143 195658143 AGGGACTCACCGCCTTGGCCAGCGCCAGCGCCAAGCGCCGAGCGCTTGGCAACCGCGACAGGCCC AGGGACTCACCGCCTTGGCCAGCGCCAGCGCCGAGCGCCGAGCGCTTGGCAACCGCGACAGGCCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195658125..195658289 26863196 MeRIP-seq:(Medium) rs1247984057 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113314 RMVar_ID_113314 Human_SNP_ID_846435579 m1A Human chr3 - 125331205 125331205 125331205 ATAGAGGGAGGAATCAGCAGCTTGGAAATTCAAGCACGTGATCTGGCGGGATGGGCGTTTGCCTA ATAGAGGGAGGAATCAGCAGCTTGGAAATTCACGCACGTGATCTGGCGGGATGGGCGTTTGCCTA T G ZNF148 Ensembl:ENSG00000163848 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:125331169..125338853 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19116032 Human_Splice_Rec_476800,Human_Splice_Rec_476801,Human_Splice_Rec_476816,Human_Splice_Rec_476817,Human_Splice_Rec_476826,Human_Splice_Rec_476827,Human_Splice_Rec_476856,Human_Splice_Rec_476857,Human_Splice_Rec_476886,Human_Splice_Rec_476887,Human_Splice_Rec_476892,Human_Splice_Rec_476893,Human_Splice_Rec_476900,Human_Splice_Rec_476901 RMVar_hsa_circ_41287,RMVar_hsa_circ_345170,RMVar_hsa_circ_278305,RMVar_hsa_circ_220872,RMVar_hsa_circ_375576,RMVar_hsa_circ_220873,RMVar_hsa_circ_290761,RMVar_hsa_circ_279728,RMVar_hsa_circ_220881,RMVar_hsa_circ_286676,RMVar_hsa_circ_61337,RMVar_hsa_circ_93452,RMVar_hsa_circ_220884,RMVar_hsa_circ_318685,RMVar_hsa_circ_220885,RMVar_hsa_circ_220888,RMVar_hsa_circ_220889,RMVar_hsa_circ_220890,RMVar_hsa_circ_378270 113315 RMVar_ID_113315 Human_SNP_ID_846466564 m1A Human chr3 - 49132344 49132344 49132344 CCGGCGCCCCTTCTCTGCTAGAGACAACCCACACAGCCATCGCATCCAGAATGTAGTCACCAGCT CCGGCGCCCCTTCTCTGCTAGAGACAACCCACGCAGCCATCGCATCCAGAATGTAGTCACCAGCT T C LAMB2 Ensembl:ENSG00000172037 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:49132251..49132425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_20912844 Human_Splice_Rec_428438,Human_Splice_Rec_428439,Human_Splice_Rec_428500,Human_Splice_Rec_428501 Human_miRNA_ID_2075430 RMVar_hsa_circ_85105,RMVar_hsa_circ_218080,RMVar_hsa_circ_124446,RMVar_hsa_circ_218108,RMVar_hsa_circ_82719,RMVar_hsa_circ_218117,RMVar_hsa_circ_124803,RMVar_hsa_circ_126769,RMVar_hsa_circ_218119,RMVar_hsa_circ_218120 113316 RMVar_ID_113316 Human_SNP_ID_846611457 m1A Human chr3 - 49163797 49163797 49163797 AAGCATCCACACCAGCCCTTGCCAAGCATGCTACCACCAACCTGCTGCTGAGCTCTCTGAAGCAA AAGCATCCACACCAGCCCTTGCCAAGCATGCTGCCACCAACCTGCTGCTGAGCTCTCTGAAGCAA T C CCDC71 Ensembl:ENSG00000177352 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49163746..49163890 26863196 MeRIP-seq:(Medium) rs374351971 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 113317 RMVar_ID_113317 Human_SNP_ID_846634285 m1A Human chr3 - 38136684 38136684 38136684 GGGGTCACTGCGGCTGCTCTTTCTGCTGCAGGACACCACCCCCGACGAGCTTCTCTCGGCAGTCA GGGGTCACTGCGGCTGCTCTTTCTGCTGCAGGGCACCACCCCCGACGAGCTTCTCTCGGCAGTCA T C ACAA1 Ensembl:ENSG00000060971 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:38136601..38136736 26863410 MeRIP-seq:(Medium) rs1198746850 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_782799,Human_RBP_ID_934945,Human_RBP_ID_5133380,Human_RBP_ID_5390608,Human_RBP_ID_8571722,Human_RBP_ID_8729752,Human_RBP_ID_19115188,Human_RBP_ID_20893484,Human_RBP_ID_22551391 Human_Splice_Rec_410954,Human_Splice_Rec_410955,Human_Splice_Rec_410972,Human_Splice_Rec_410973,Human_Splice_Rec_410990,Human_Splice_Rec_410991,Human_Splice_Rec_411014,Human_Splice_Rec_411015,Human_Splice_Rec_411034,Human_Splice_Rec_411035,Human_Splice_Rec_411082,Human_Splice_Rec_411083,Human_Splice_Rec_411117,Human_Splice_Rec_411134,Human_Splice_Rec_411135,Human_Splice_Rec_411148,Human_Splice_Rec_411149,Human_Splice_Rec_411158,Human_Splice_Rec_411159,Human_Splice_Rec_411174,Human_Splice_Rec_411175,Human_Splice_Rec_411186,Human_Splice_Rec_411187,Human_Splice_Rec_411190,Human_Splice_Rec_411191,Human_Splice_Rec_411196,Human_Splice_Rec_411197 RMVar_hsa_circ_89235,RMVar_hsa_circ_217061,RMVar_hsa_circ_108622,RMVar_hsa_circ_217064,RMVar_hsa_circ_76566,RMVar_hsa_circ_217063 113318 RMVar_ID_113318 Human_SNP_ID_846653515 m1A Human chr3 + 146161002 146161002 146161002 TTCACCGTGCATCCCCCCATATTCGGCCCTCGAGGGCCGCGCGGGCTCAGGCGCCCACGGCCCCG TTCACCGTGCATCCCCCCATATTCGGCCCTCGGGGGCCGCGCGGGCTCAGGCGCCCACGGCCCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr3:146160951..146161269;chr3:146160964..146161255;chr3:146160951..146161175 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 113319 RMVar_ID_113319 Human_SNP_ID_846653520 m1A Human chr3 + 146161002 146161002 146161002 TTCACCGTGCATCCCCCCATATTCGGCCCTCGAGGGCCGCGCGGGCTCAGGCGCCCACGGCCCCG TTCACCGTGCATCCCCCCATATTCGGCCCTCGCGGGCCGCGCGGGCTCAGGCGCCCACGGCCCCG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr3:146160951..146161269;chr3:146160964..146161255;chr3:146160951..146161175 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast 113320 RMVar_ID_113320 Human_SNP_ID_846665451 m1A Human chr3 + 183884771 183884771 183884771 CGGCGGGGTTAGGACCGCAGTGAGCTCCTCGCAGCTGCGGCCGCCCACCGACGCACCCCACGCCT CGGCGGGGTTAGGACCGCAGTGAGCTCCTCGCTGCTGCGGCCGCCCACCGACGCACCCCACGCCT A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr3:183884701..183884875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113321 RMVar_ID_113321 Human_SNP_ID_846668460 m1A Human chr3 + 14178880 14178880 14178880 CAGGGTTTGAAACATGGCGGACGACGTAGACCAGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG CAGGGTTTGAAACATGGCGGACGACGTAGACCCGGTAAGTGTATTTTAAGGAGGTCGCTCGAAGG A C LSM3 Ensembl:ENSG00000170860 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:14178826..14178900 26863410 MeRIP-seq:(Medium) rs200658802 Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_9393339 Human_Splice_Rec_397301 113322 RMVar_ID_113322 Human_SNP_ID_846673066 m1A Human chr3 - 39407646 39407646 39407646 GCAGGACATCAAGGGCTCCGGACATTGTGAAAATTTCCCTTTAAGTTACGACGGGAATCTGAAAT GCAGGACATCAAGGGCTCCGGACATTGTGAAAGTTTCCCTTTAAGTTACGACGGGAATCTGAAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:39407601..39407700 32194978 MeRIP-seq:(Medium) rs1803893 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue 113323 RMVar_ID_113323 Human_SNP_ID_846703596 m1A Human chr3 + 187743790 187743790 187743790 CTCAGCCGATTTCTGAGGCTCCAACTCTACCCACTCCCTCCCCGGGCCGCCGCCGCCGCGCCTTC CTCAGCCGATTTCTGAGGCTCCAACTCTACCCCCTCCCTCCCCGGGCCGCCGCCGCCGCGCCTTC A C AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:187743787..187743975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113324 RMVar_ID_113324 Human_SNP_ID_846720978 m1A Human chr3 - 158572818 158572818 158572818 GGCCCTCAACTCTCTACCTCACGTCCTCAACCATCCTCCTGCGACCTCACGCCCCCAAACCCTCC GGCCCTCAACTCTCTACCTCACGTCCTCAACCCTCCTCCTGCGACCTCACGCCCCCAAACCCTCC T G lnc-LXN-3 RNACentral:URS00008B36CA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:158572735..158572939 26863196 MeRIP-seq:(Medium) rs17629390 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_10076,GWAS_ID_10077,GWAS_ID_10078 113325 RMVar_ID_113325 Human_SNP_ID_846839890 m1A Human chr3 - 158571276 158571276 158571276 CTGAACATTCTGGCTCTGTCTTGGGTGGCGGCAGCCGCGGACAGATTGGAAAAACGATGTTAACT CTGAACATTCTGGCTCTGTCTTGGGTGGCGGCCGCCGCGGACAGATTGGAAAAACGATGTTAACT T G lnc-LXN-3 RNACentral:URS00008B36CA lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:158571228..158571324 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus 113326 RMVar_ID_113326 Human_SNP_ID_846883464 m1A Human chr3 - 182980489 182980489 182980489 AGGAGGAGGGGAGAGGCCTGGAGGACACCAACATGGTGAGGCACTGCGGCCGCCCGCCCGCCCTG AGGAGGAGGGGAGAGGCCTGGAGGACACCAACTTGGTGAGGCACTGCGGCCGCCCGCCCGCCCTG T A DCUN1D1 Ensembl:ENSG00000043093 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:182980366..182980492 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_835143,Human_RBP_ID_4758962,Human_RBP_ID_5654717,Human_RBP_ID_18424098,Human_RBP_ID_26347435,Human_RBP_ID_27822740 Human_Splice_Rec_513047,Human_Splice_Rec_513059,Human_Splice_Rec_513095 113327 RMVar_ID_113327 Human_SNP_ID_846886303 m1A Human chr3 + 197782055 197782055 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTTAAAAAAAAAACGTATAAAATAATGCCCTGAAA A T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs532153464 Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,oesophagus adenocarcinoma,ESCA 7 oesophagus,pancreas Human_RBP_ID_69843,Human_RBP_ID_598524 113328 RMVar_ID_113328 Human_SNP_ID_846890921 m1A Human chr3 - 16259118 16259118 16259118 CTCACTCACTATGGTGGCATCAGCTGCAAAGCAAAATGAACTGTCCCATGATCATGTTGATGGTT CTCACTCACTATGGTGGCATCAGCTGCAAAGCGAAATGAACTGTCCCATGATCATGTTGATGGTT T C DPH3 Ensembl:ENSG00000154813 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs842254 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8869319 GWAS_ID_7068,GWAS_ID_7069,GWAS_ID_7070,GWAS_ID_7071,GWAS_ID_7072,GWAS_ID_7073,GWAS_ID_7074,GWAS_ID_7075,GWAS_ID_7076,GWAS_ID_7077,GWAS_ID_7078,GWAS_ID_7079,GWAS_ID_7080,GWAS_ID_7081,GWAS_ID_7082,GWAS_ID_7083,GWAS_ID_7084,GWAS_ID_7085,GWAS_ID_7086,GWAS_ID_7087,GWAS_ID_7088,GWAS_ID_7089,GWAS_ID_7090,GWAS_ID_7091,GWAS_ID_7092,GWAS_ID_7093,GWAS_ID_7094,GWAS_ID_7095,GWAS_ID_7096,GWAS_ID_7097,GWAS_ID_7098,GWAS_ID_7099,GWAS_ID_7100,GWAS_ID_7101,GWAS_ID_7102,GWAS_ID_7103,GWAS_ID_7104,GWAS_ID_7105,GWAS_ID_7106,GWAS_ID_7107,GWAS_ID_7108,GWAS_ID_7109,GWAS_ID_7110,GWAS_ID_7111,GWAS_ID_7112,GWAS_ID_7113,GWAS_ID_7114,GWAS_ID_7115,GWAS_ID_7116,GWAS_ID_7117,GWAS_ID_7118,GWAS_ID_7119,GWAS_ID_7120,GWAS_ID_7121,GWAS_ID_7122,GWAS_ID_7123,GWAS_ID_7124,GWAS_ID_7125,GWAS_ID_7126,GWAS_ID_7127,GWAS_ID_7128,GWAS_ID_7129,GWAS_ID_7130,GWAS_ID_7131,GWAS_ID_7132,GWAS_ID_7133,GWAS_ID_7134,GWAS_ID_7135,GWAS_ID_7136,GWAS_ID_7137,GWAS_ID_7138,GWAS_ID_7139,GWAS_ID_7140,GWAS_ID_7141,GWAS_ID_7142,GWAS_ID_7143,GWAS_ID_7144,GWAS_ID_7145,GWAS_ID_7146,GWAS_ID_7147,GWAS_ID_7148,GWAS_ID_7149,GWAS_ID_7150,GWAS_ID_7151,GWAS_ID_7152,GWAS_ID_7153,GWAS_ID_7154,GWAS_ID_7155,GWAS_ID_7156,GWAS_ID_7157,GWAS_ID_7158,GWAS_ID_7159,GWAS_ID_7160,GWAS_ID_7161,GWAS_ID_7162,GWAS_ID_7163,GWAS_ID_7164,GWAS_ID_7165,GWAS_ID_7166,GWAS_ID_7167,GWAS_ID_7168,GWAS_ID_7169,GWAS_ID_7170,GWAS_ID_7171,GWAS_ID_7172,GWAS_ID_7173,GWAS_ID_7174,GWAS_ID_7175,GWAS_ID_7176,GWAS_ID_7177,GWAS_ID_7178,GWAS_ID_7179,GWAS_ID_7180,GWAS_ID_7181,GWAS_ID_7182,GWAS_ID_7183,GWAS_ID_7184,GWAS_ID_7185,GWAS_ID_7186,GWAS_ID_7187,GWAS_ID_7188,GWAS_ID_7189,GWAS_ID_7190,GWAS_ID_7191,GWAS_ID_7192,GWAS_ID_7193,GWAS_ID_7194,GWAS_ID_7195,GWAS_ID_7196,GWAS_ID_7197,GWAS_ID_7198,GWAS_ID_7199,GWAS_ID_7200,GWAS_ID_7201,GWAS_ID_7202,GWAS_ID_7203,GWAS_ID_7204,GWAS_ID_7205,GWAS_ID_7206,GWAS_ID_7207,GWAS_ID_7208,GWAS_ID_7209,GWAS_ID_7210,GWAS_ID_7211,GWAS_ID_7212,GWAS_ID_7213,GWAS_ID_7214,GWAS_ID_7215,GWAS_ID_7216,GWAS_ID_7217,GWAS_ID_7218,GWAS_ID_7219,GWAS_ID_7220,GWAS_ID_7221,GWAS_ID_7222,GWAS_ID_7223,GWAS_ID_7224,GWAS_ID_7225,GWAS_ID_7226,GWAS_ID_7227,GWAS_ID_7228,GWAS_ID_7229,GWAS_ID_7230,GWAS_ID_7231,GWAS_ID_7232,GWAS_ID_7233,GWAS_ID_7234,GWAS_ID_7235,GWAS_ID_7236,GWAS_ID_7237,GWAS_ID_7238,GWAS_ID_7239,GWAS_ID_7240,GWAS_ID_7241,GWAS_ID_7242,GWAS_ID_7243,GWAS_ID_7244,GWAS_ID_7245,GWAS_ID_7246,GWAS_ID_7247,GWAS_ID_7248,GWAS_ID_7249,GWAS_ID_7250,GWAS_ID_7251,GWAS_ID_7252,GWAS_ID_7253,GWAS_ID_7254,GWAS_ID_7255,GWAS_ID_7256,GWAS_ID_7257,GWAS_ID_7258,GWAS_ID_7259,GWAS_ID_7260,GWAS_ID_7261 113329 RMVar_ID_113329 Human_SNP_ID_846898142 m1A Human chr3 - 129589401 129589401 129589401 CGGGCCTCACCTCCGTGGCCGTGGCCAGCGTCAACAACTACACAGCGGTCTTCCTGGGCACGGTC CGGGCCTCACCTCCGTGGCCGTGGCCAGCGTCGACAACTACACAGCGGTCTTCCTGGGCACGGTC T C PLXND1 Ensembl:ENSG00000004399 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129589314..129589459 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18194718 Human_Splice_Rec_481697,Human_Splice_Rec_481861 Human_miRNA_ID_3056970 RMVar_hsa_circ_120545,RMVar_hsa_circ_221179,RMVar_hsa_circ_36121,RMVar_hsa_circ_347039,RMVar_hsa_circ_110575,RMVar_hsa_circ_221188,RMVar_hsa_circ_221190,RMVar_hsa_circ_363859,RMVar_hsa_circ_36330 113330 RMVar_ID_113330 Human_SNP_ID_846908693 m1A Human chr3 - 47661389 47661389 47661389 GGAATTGGTTGAAGCTCATGTCAAGAAAGTACAAGAAGCAGCACGAGCCTCTGGGAAAGTGGATC GGAATTGGTTGAAGCTCATGTCAAGAAAGTACGAGAAGCAGCACGAGCCTCTGGGAAAGTGGATC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:47661214..47661450 26863196 MeRIP-seq:(Medium) rs768188371 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_68972,Human_RBP_ID_1627734,Human_RBP_ID_1963806,Human_RBP_ID_2787281,Human_RBP_ID_4744032,Human_RBP_ID_9393519,Human_RBP_ID_22281748,Human_RBP_ID_22823685,Human_RBP_ID_26823790 Human_Splice_Rec_422864,Human_Splice_Rec_422865,Human_Splice_Rec_422916,Human_Splice_Rec_422917 RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_41465,RMVar_hsa_circ_217644,RMVar_hsa_circ_217646,RMVar_hsa_circ_217647,RMVar_hsa_circ_217645,RMVar_hsa_circ_302167,RMVar_hsa_circ_323863,RMVar_hsa_circ_217643,RMVar_hsa_circ_355847,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_15213,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_217663,RMVar_hsa_circ_298792,RMVar_hsa_circ_342559,RMVar_hsa_circ_375152,RMVar_hsa_circ_308076,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217669,RMVar_hsa_circ_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665,RMVar_hsa_circ_112057,RMVar_hsa_circ_294805,RMVar_hsa_circ_318682,RMVar_hsa_circ_367020,RMVar_hsa_circ_217668,RMVar_hsa_circ_343286,RMVar_hsa_circ_317580,RMVar_hsa_circ_274119,RMVar_hsa_circ_276369,RMVar_hsa_circ_272889,RMVar_hsa_circ_217672,RMVar_hsa_circ_37658,RMVar_hsa_circ_64960,RMVar_hsa_circ_217674,RMVar_hsa_circ_217675,RMVar_hsa_circ_217673,RMVar_hsa_circ_217670,RMVar_hsa_circ_217671 113331 RMVar_ID_113331 Human_SNP_ID_846909059 m1A Human chr3 + 187745289 187745289 187745289 ACTTGGAGCCAAAGCATTTGGCAAGAGCGGAAAAAAAAAGAATTAAAAGGTAAAATAATGATCAT ACTTGGAGCCAAAGCATTTGGCAAGAGCGGAATAAAAAAGAATTAAAAGGTAAAATAATGATCAT A T AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:187745287..187745426;chr3:187745287..187745421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_Splice_Rec_522554 113332 RMVar_ID_113332 Human_SNP_ID_846909073 m1A Human chr3 + 187745289 187745289 187745289 ACTTGGAGCCAAAGCATTTGGCAAGAGCGGAAAAAAAAAGAATTAAAAGGTAAAATAATGATCAT ACTTGGAGCCAAAGCATTTGGCAAGAGCGGAAGAAAAAAGAATTAAAAGGTAAAATAATGATCAT A G AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:187745287..187745426;chr3:187745287..187745421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_Splice_Rec_522554 113333 RMVar_ID_113333 Human_SNP_ID_846921234 m1A Human chr3 + 156555059 156555059 156555059 GCTGAAATCCTGCAGGAGCAGGTCCTCCTCAGACTGCTGTTTGGAGCTGCCTTTAGGAGCCATGG GCTGAAATCCTGCAGGAGCAGGTCCTCCTCAGTCTGCTGTTTGGAGCTGCCTTTAGGAGCCATGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:156555010..156555100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 113334 RMVar_ID_113334 Human_SNP_ID_846931204 m1A Human chr3 + 155987852 155987852 155987852 TGGAAATCTGGAAAGGATTTGACGAAACGTTCAAGTCAAACACAGAATAAAGCCAGCAGGAAGAG TGGAAATCTGGAAAGGATTTGACGAAACGTTCGAGTCAAACACAGAATAAAGCCAGCAGGAAGAG A G SETP14 Ensembl:ENSG00000240489 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs185557603 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_3723402,Human_RBP_ID_17405847,Human_RBP_ID_18014503 113335 RMVar_ID_113335 Human_SNP_ID_846938157 m1A Human chr3 + 40310968 40310968 40310968 AGGGACTGAGGATTACATTCATATAAGAATCCAGCAACGGAACGGCAGAAAGACACTGACTACTG AGGGACTGAGGATTACATTCATATAAGAATCCTGCAACGGAACGGCAGAAAGACACTGACTACTG A T EIF1B Ensembl:ENSG00000114784 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:40310873..40310968 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_248223,Human_RBP_ID_785258,Human_RBP_ID_1626508,Human_RBP_ID_17291326,Human_RBP_ID_17404549,Human_RBP_ID_22823330,Human_RBP_ID_27052201 Human_Splice_Rec_414016,Human_Splice_Rec_414017,Human_Splice_Rec_414022,Human_Splice_Rec_414024,Human_Splice_Rec_414025,Human_Splice_Rec_414027 RMVar_hsa_circ_6835,RMVar_hsa_circ_217144 113336 RMVar_ID_113336 Human_SNP_ID_846946333 m1A Human chr3 + 9834698 9834601 9834699 CTCTTGCTCCCACAGCCCGTCACCACTTCCCCAGCCTCCACACCAAGGCCCAGCTGCCTTCTCCC __________________________________CCTCCACACCAAGGCCCAGCTGCCTTCTCCC TCCTCCACACGTACCTGTTAGGGCAGCTAGGCCACCTTGGGCCCCACCCCAGGGCCTCACAGCTTCTCTTGCTCCCACAGCCCGTCACCACTTCCCCAG T ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:9834595..9834718 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 1..34 33 PRAD 1 - Human_RBP_ID_18169716 Human_Splice_Rec_390828,Human_Splice_Rec_390926,Human_Splice_Rec_390988,Human_Splice_Rec_391018,Human_Splice_Rec_391034,Human_Splice_Rec_391072,Human_Splice_Rec_391080,Human_Splice_Rec_391092,Human_Splice_Rec_391108,Human_Splice_Rec_391132 113337 RMVar_ID_113337 Human_SNP_ID_846962792 m1A Human chr3 - 111946932 111946932 111946932 CTCTACCTCCAAAATACCTGCTAATCCAGCTAACTCCTTCTATCTCTCTGCCATCCTCCAATTCA CTCTACCTCCAAAATACCTGCTAATCCAGCTAGCTCCTTCTATCTCTCTGCCATCCTCCAATTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:111946882..111946955 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113338 RMVar_ID_113338 Human_SNP_ID_846988189 m1A Human chr3 - 9902934 9902934 9902934 GCAGGAGCAGGGCTGCCAGTCTGGAGCTCCCCATGGGCTTCTGTGCAATTAGGGCTCCCGGAACA GCAGGAGCAGGGCTGCCAGTCTGGAGCTCCCCGTGGGCTTCTGTGCAATTAGGGCTCCCGGAACA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:9902883..9903000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113339 RMVar_ID_113339 Human_SNP_ID_846993476 m1A Human chr3 - 139371802 139371802 139371802 GGTTTGTGGTGGTGTGTGGTGATGGGGAGTATATCATCTACACAGCAATGGCATTGAGAAACAAG GGTTTGTGGTGGTGTGTGGTGATGGGGAGTATGTCATCTACACAGCAATGGCATTGAGAAACAAG T C COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:139371751..139374264 32194978 MeRIP-seq:(Medium) rs1263754828 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8875646,Human_RBP_ID_9132819,Human_RBP_ID_9354424,Human_RBP_ID_22457018,Human_RBP_ID_25763208 Human_Splice_Rec_489828,Human_Splice_Rec_489829,Human_Splice_Rec_489870,Human_Splice_Rec_489871,Human_Splice_Rec_489897 RMVar_hsa_circ_121631,RMVar_hsa_circ_119393,RMVar_hsa_circ_103134,RMVar_hsa_circ_106324,RMVar_hsa_circ_96987,RMVar_hsa_circ_221749,RMVar_hsa_circ_93453,RMVar_hsa_circ_221751,RMVar_hsa_circ_221750,RMVar_hsa_circ_103906,RMVar_hsa_circ_221747,RMVar_hsa_circ_221748,RMVar_hsa_circ_221746,RMVar_hsa_circ_221758,RMVar_hsa_circ_348730,RMVar_hsa_circ_101913,RMVar_hsa_circ_57059,RMVar_hsa_circ_221759,RMVar_hsa_circ_65898,RMVar_hsa_circ_37084 113340 RMVar_ID_113340 Human_SNP_ID_847016402 m1A Human chr3 + 49929706 49929706 49929706 AGGGGTAAGGGTGTCCGGCCGGGGCCGGCCTGAGGGCACAGCTTCGCGGGGCCCCGGCCCCCTGC AGGGGTAAGGGTGTCCGGCCGGGGCCGGCCTGCGGGCACAGCTTCGCGGGGCCCCGGCCCCCTGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:49929656..49929841 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113341 RMVar_ID_113341 Human_SNP_ID_847038596 m1A Human chr3 + 192409308 192409308 192409308 CAAAAGGCAGCGATGCCGAAGGTGTCCTCTCCAGCTCGGCGCCCACACGCCTTTAACTGGAGCTC CAAAAGGCAGCGATGCCGAAGGTGTCCTCTCCGGCTCGGCGCCCACACGCCTTTAACTGGAGCTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:192409258..192409362 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113342 RMVar_ID_113342 Human_SNP_ID_847051388 m1A Human chr3 - 53225803 53225803 53225803 CGGCTGAGCTGCTGAAGATGTTTGGTATCGACAGGGATGCCATTGCACAAGCTGTGAGGGGCCTC CGGCTGAGCTGCTGAAGATGTTTGGTATCGACCGGGATGCCATTGCACAAGCTGTGAGGGGCCTC T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:53225651..53225868 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_606034,Human_RBP_ID_783754,Human_RBP_ID_934411,Human_RBP_ID_1629894,Human_RBP_ID_3964129,Human_RBP_ID_17660718,Human_RBP_ID_17704407,Human_RBP_ID_24011923 Human_Splice_Rec_441223 Human_miRNA_ID_2421350,Human_miRNA_ID_2443556 RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_348857 113343 RMVar_ID_113343 Human_SNP_ID_847072414 m1A Human chr3 - 44750062 44750062 44750062 CACCCAGGCCAGACACAATGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCCAAGGTGGGAGA CACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTGGGAAGCCAAGGTGGGAGA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs372844577 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,biliary_tract adenocarcinoma,central_nervous_system astrocytoma_Grade_IV,gallbladder adenocarcinoma,brain astrocytoma_Grade_IV 3 biliary tract,gallbladder,brain Human_RBP_ID_4742340 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 113344 RMVar_ID_113344 Human_SNP_ID_847080407 m1A Human chr3 + 184302482 184302482 184302482 TCCCTGAAGCTCTGAGATTGGCATTGATGCTCAATGACATGGAGTTGGTAGAAGACATCTTCACC TCCCTGAAGCTCTGAGATTGGCATTGATGCTCCATGACATGGAGTTGGTAGAAGACATCTTCACC A C PSMD2 Ensembl:ENSG00000175166 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184302432..184302549 26863196 MeRIP-seq:(Medium) rs767466862 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_596594,Human_RBP_ID_1957453,Human_RBP_ID_9395735,Human_RBP_ID_14745124,Human_RBP_ID_24535589 Human_Splice_Rec_516451,Human_Splice_Rec_516477,Human_Splice_Rec_516529,Human_Splice_Rec_516537,Human_Splice_Rec_516573,Human_Splice_Rec_516611,Human_Splice_Rec_516613 Human_miRNA_ID_2938147 RMVar_hsa_circ_83352,RMVar_hsa_circ_13178,RMVar_hsa_circ_32647,RMVar_hsa_circ_116451,RMVar_hsa_circ_223344,RMVar_hsa_circ_71174,RMVar_hsa_circ_95935,RMVar_hsa_circ_106166,RMVar_hsa_circ_223345,RMVar_hsa_circ_223346,RMVar_hsa_circ_290355,RMVar_hsa_circ_54591,RMVar_hsa_circ_127780,RMVar_hsa_circ_223347,RMVar_hsa_circ_223349,RMVar_hsa_circ_119144,RMVar_hsa_circ_351976,RMVar_hsa_circ_74682,RMVar_hsa_circ_223350 113345 RMVar_ID_113345 Human_SNP_ID_847097874 m1A Human chr3 + 184321481 184321481 184321481 ACTATGACAACTATACAAATGTCTGTAGAAGAATCAACCCCCATCTCCCGTGAAACTGGGGAGCC ACTATGACAACTATACAAATGTCTGTAGAAGATTCAACCCCCATCTCCCGTGAAACTGGGGAGCC A T EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:184321354..184321637 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 13 head and neck Human_RBP_ID_67236,Human_RBP_ID_1623337,Human_RBP_ID_1957497,Human_RBP_ID_4733518,Human_RBP_ID_8567094,Human_RBP_ID_8870134,Human_RBP_ID_9261193,Human_RBP_ID_9333974,Human_RBP_ID_14745240,Human_RBP_ID_17289369,Human_RBP_ID_17402752,Human_RBP_ID_17518770,Human_RBP_ID_18001231,Human_RBP_ID_18803716,Human_RBP_ID_18954769,Human_RBP_ID_23020912,Human_RBP_ID_27049693,Human_RBP_ID_27316084 Human_miRNA_ID_3011330,Human_miRNA_ID_3011331 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 113346 RMVar_ID_113346 Human_SNP_ID_847105736 m1A Human chr3 + 184322014 184322014 184322014 AGAAGCAGGAGAAGCAGGAGAAGCTGAGAGTGAGAAAGGAGGAGAGGAACTGCTCCCCCCAGAGA AGAAGCAGGAGAAGCAGGAGAAGCTGAGAGTGTGAAAGGAGGAGAGGAACTGCTCCCCCCAGAGA A T EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:184321794..184322050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 CHOL 1 - Human_RBP_ID_934070,Human_RBP_ID_1957505,Human_RBP_ID_3699307,Human_RBP_ID_4763309,Human_RBP_ID_7167758,Human_RBP_ID_8567105,Human_RBP_ID_8870150,Human_RBP_ID_9302625,Human_RBP_ID_9334374,Human_RBP_ID_9394340,Human_RBP_ID_18803732,Human_RBP_ID_23989285,Human_RBP_ID_24547350,Human_RBP_ID_26346352,Human_RBP_ID_27049701,Human_RBP_ID_27822786 Human_Splice_Rec_516683,Human_Splice_Rec_516747,Human_Splice_Rec_516805,Human_Splice_Rec_516867,Human_Splice_Rec_516929,Human_Splice_Rec_516961,Human_Splice_Rec_516995,Human_Splice_Rec_517055,Human_Splice_Rec_517089,Human_Splice_Rec_517125,Human_Splice_Rec_517181,Human_Splice_Rec_517277,Human_Splice_Rec_517339,Human_Splice_Rec_517401,Human_Splice_Rec_517469,Human_Splice_Rec_517523,Human_Splice_Rec_517551,Human_Splice_Rec_517607,Human_Splice_Rec_517673 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 113347 RMVar_ID_113347 Human_SNP_ID_847133028 m1A Human chr3 + 8752936 8752936 8752936 ATCACCTAGGAGCAGAGCACTTATGCCAGCACAGCCTGAGCCTCAGGCTGCAGCCCTGGCCCTGG ATCACCTAGGAGCAGAGCACTTATGCCAGCACCGCCTGAGCCTCAGGCTGCAGCCCTGGCCCTGG A C CAV3 Ensembl:ENSG00000182533 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:8752887..8753125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113348 RMVar_ID_113348 Human_SNP_ID_847151594 m1A Human chr3 - 158102849 158102849 158102849 CCGGAGCTGAAAGATCGCAAAGAGGATGCGAAAGGGATGGAGGACGAAGGCCAGACCAAAATCAA CCGGAGCTGAAAGATCGCAAAGAGGATGCGAACGGGATGGAGGACGAAGGCCAGACCAAAATCAA T G SHOX2 Ensembl:ENSG00000168779 Protein coding exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:158102726..158102865 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_Splice_Rec_499632,Human_Splice_Rec_499644,Human_Splice_Rec_499650,Human_Splice_Rec_499658 RMVar_hsa_circ_121983,RMVar_hsa_circ_222358 113349 RMVar_ID_113349 Human_SNP_ID_847152611 m1A Human chr3 - 101562005 101562005 101562005 CACACACATTAGGCGAAAGAAGAAACTCGCTTACCAGGAGTGCAGAGATAGTGGTTCCCGCTGGC CACACACATTAGGCGAAAGAAGAAACTCGCTTCCCAGGAGTGCAGAGATAGTGGTTCCCGCTGGC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:101561960..101562098 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach 113350 RMVar_ID_113350 Human_SNP_ID_847157928 m1A Human chr3 - 127616933 127616933 127616933 GGACACTTTCTCAATATACTTGAGAAACTGCGACTTCGCTGTGCCAGGGTCTCCGCACAAGAGCA GGACACTTTCTCAATATACTTGAGAAACTGCGGCTTCGCTGTGCCAGGGTCTCCGCACAAGAGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:127616851..127617025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine 113351 RMVar_ID_113351 Human_SNP_ID_847158079 m1A Human chr3 + 27633157 27633157 27633157 CCCTCAACCGACGCATCCAGCTCGTTGAGGAGAAGTTGGACAGGGCTCAGGAAAGACTGGCCACG CCCTCAACCGACGCATCCAGCTCGTTGAGGAGGAGTTGGACAGGGCTCAGGAAAGACTGGCCACG A G AC098614.2 Ensembl:ENSG00000271943 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1320428615 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_miRNA_ID_1859387 113352 RMVar_ID_113352 Human_SNP_ID_847167171 m1A Human chr3 - 49026595 49026595 49026595 ACTTACTTCTTGTCCTAGGACTCTTCCCAGGGAAATTCCATCTTCCAGATCAATATGATCAAGTA ACTTACTTCTTGTCCTAGGACTCTTCCCAGGGCAATTCCATCTTCCAGATCAATATGATCAAGTA T G IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49026501..49027925 32194978 MeRIP-seq:(Medium) rs1168426638 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_69237,Human_RBP_ID_604024,Human_RBP_ID_933744,Human_RBP_ID_1033593,Human_RBP_ID_1069172,Human_RBP_ID_2789007,Human_RBP_ID_3965175,Human_RBP_ID_5390761,Human_RBP_ID_8873021,Human_RBP_ID_19120549,Human_RBP_ID_22456608,Human_RBP_ID_22745179 Human_Splice_Rec_427134,Human_Splice_Rec_427135,Human_Splice_Rec_427162,Human_Splice_Rec_427163,Human_Splice_Rec_427190,Human_Splice_Rec_427191,Human_Splice_Rec_427204,Human_Splice_Rec_427208 RMVar_hsa_circ_93264,RMVar_hsa_circ_113558,RMVar_hsa_circ_115625,RMVar_hsa_circ_110033,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,RMVar_hsa_circ_218036,RMVar_hsa_circ_218035,RMVar_hsa_circ_218032,RMVar_hsa_circ_218033,RMVar_hsa_circ_64720,RMVar_hsa_circ_108727,RMVar_hsa_circ_372346,RMVar_hsa_circ_300468,RMVar_hsa_circ_371174,RMVar_hsa_circ_94815,RMVar_hsa_circ_26823,RMVar_hsa_circ_218039,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_218040,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043 113353 RMVar_ID_113353 Human_SNP_ID_847205395 m1A Human chr3 - 47805279 47805279 47805279 GCTGAGTCAATACAGTGGAGGCCCCATAGGGAAAGAAAGTTGCTCCAACCATCATTTACTAGCTC GCTGAGTCAATACAGTGGAGGCCCCATAGGGACAGAAAGTTGCTCCAACCATCATTTACTAGCTC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47805277..47805349 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 meninges atypical 2 brain 113354 RMVar_ID_113354 Human_SNP_ID_847219055 m1A Human chr3 - 53235030 53235030 53235030 ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCACTGCAGCACCAGATGGACATCTACCAGAAGCG ATCAATCGCCTGGGCCAGAGTGACCCGGCCCCGCTGCAGCACCAGATGGACATCTACCAGAAGCG T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:53234890..53235077 26863196 MeRIP-seq:(Medium) rs1051485 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_68527,Human_RBP_ID_606074,Human_RBP_ID_783770,Human_RBP_ID_835695,Human_RBP_ID_7211418,Human_RBP_ID_9302935,Human_RBP_ID_18194643,Human_RBP_ID_22456734,Human_RBP_ID_22769319,Human_RBP_ID_22824733,Human_RBP_ID_26823956,Human_RBP_ID_27057530 Human_Splice_Rec_441179,Human_Splice_Rec_441205,Human_Splice_Rec_441256,Human_Splice_Rec_441257,Human_Splice_Rec_441285,Human_Splice_Rec_441309,Human_Splice_Rec_441335,Human_Splice_Rec_441365,Human_Splice_Rec_441371 GWAS_ID_10758,GWAS_ID_10759,GWAS_ID_10760,GWAS_ID_10761,GWAS_ID_10762,GWAS_ID_10763,GWAS_ID_10764,GWAS_ID_10765,GWAS_ID_10766,GWAS_ID_10767,GWAS_ID_10768,GWAS_ID_10769,GWAS_ID_10770,GWAS_ID_10771,GWAS_ID_10772,GWAS_ID_10773,GWAS_ID_10774,GWAS_ID_10775,GWAS_ID_10776,GWAS_ID_10777,GWAS_ID_10778,GWAS_ID_10779,GWAS_ID_10780,GWAS_ID_10781,GWAS_ID_10782,GWAS_ID_10783,GWAS_ID_10784,GWAS_ID_10785,GWAS_ID_10786,GWAS_ID_10787,GWAS_ID_10788,GWAS_ID_10789,GWAS_ID_10790,GWAS_ID_10791,GWAS_ID_10792,GWAS_ID_10793,GWAS_ID_10794,GWAS_ID_10795,GWAS_ID_10796,GWAS_ID_10797,GWAS_ID_10798,GWAS_ID_10799,GWAS_ID_10800,GWAS_ID_10801,GWAS_ID_10802,GWAS_ID_10803,GWAS_ID_10804,GWAS_ID_10805,GWAS_ID_10806,GWAS_ID_10807,GWAS_ID_10808,GWAS_ID_10809,GWAS_ID_10810,GWAS_ID_10811,GWAS_ID_10812,GWAS_ID_10813,GWAS_ID_10814,GWAS_ID_10815 RMVar_hsa_circ_9067,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_119151,RMVar_hsa_circ_218883,RMVar_hsa_circ_374561,RMVar_hsa_circ_371400,RMVar_hsa_circ_218886,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_281638,RMVar_hsa_circ_31346 113355 RMVar_ID_113355 Human_SNP_ID_847273412 m1A Human chr3 + 43691034 43691032 43691034 GAGGAGGAGGAGGTGGACTCTGCCGACACCGGAGAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GAGGAGGAGGAGGTGGACTCTGCCGACACCG__GAGAGGTAAGCGCAGCCGGCAGGGGGCTTCGT GGA G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:43690924..43691262 26863196 MeRIP-seq:(Medium) rs387906336 Functional Loss DEL TCGA 32..33 33 LUAD 1 - Human_RBP_ID_602123,Human_RBP_ID_4757134,Human_RBP_ID_23115855 Human_Splice_Rec_417959,Human_Splice_Rec_417969,Human_Splice_Rec_417971,Human_Splice_Rec_417985,Human_Splice_Rec_417993,Human_Splice_Rec_418003,Human_Splice_Rec_418015,Human_Splice_Rec_418027,Human_Splice_Rec_418041,Human_Splice_Rec_418051 Clinvar_Rec_638 113356 RMVar_ID_113356 Human_SNP_ID_847326071 m1A Human chr3 - 48609287 48609287 48609287 GCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGACGCCAGCCTTGCGGAGTACGGCAACCTTCGCT GCTGTTCCCTTCCACAGCCGGCCCTGCTGCGGGCGCCAGCCTTGCGGAGTACGGCAACCTTCGCT T C UQCRC1 Ensembl:ENSG00000010256 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48609176..48609355 26863410 MeRIP-seq:(Medium) rs370111314 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 1 head and neck Human_RBP_ID_246970,Human_RBP_ID_603563,Human_RBP_ID_834490,Human_RBP_ID_4745011,Human_RBP_ID_8875497,Human_RBP_ID_8943485,Human_RBP_ID_9302304,Human_RBP_ID_22455810 Human_Splice_Rec_425374,Human_Splice_Rec_425442,Human_Splice_Rec_425452,Human_Splice_Rec_425460 RMVar_hsa_circ_102894,RMVar_hsa_circ_79147,RMVar_hsa_circ_217923,RMVar_hsa_circ_217922,RMVar_hsa_circ_88549,RMVar_hsa_circ_108049,RMVar_hsa_circ_217938,RMVar_hsa_circ_45708,RMVar_hsa_circ_120659,RMVar_hsa_circ_217940,RMVar_hsa_circ_122606,RMVar_hsa_circ_217942,RMVar_hsa_circ_217944,RMVar_hsa_circ_76431,RMVar_hsa_circ_217943 113357 RMVar_ID_113357 Human_SNP_ID_847330362 m1A Human chr3 + 49028321 49028321 49028321 AGTTGTGGTGGATGAAGCCAATACCGCCTGTAAGCTACAGGATAAAAAGAGACTACTACTAAGTG AGTTGTGGTGGATGAAGCCAATACCGCCTGTACGCTACAGGATAAAAAGAGACTACTACTAAGTG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49028249..49028342 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 2 kidney 113358 RMVar_ID_113358 Human_SNP_ID_847359488 m1A Human chr3 + 128910087 128910087 128910087 TGGCCAACATCCTCATCAACCTGTATGGCATGACGGCCGTGCTGTCGCGGGCCAGCCGCTCCATC TGGCCAACATCCTCATCAACCTGTATGGCATGTCGGCCGTGCTGTCGCGGGCCAGCCGCTCCATC A T ACAD9 Ensembl:ENSG00000177646 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:128909964..128910150;chr3:128909915..128910122 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_480016,Human_Splice_Rec_480017,Human_Splice_Rec_480072,Human_Splice_Rec_480073,Human_Splice_Rec_480116,Human_Splice_Rec_480117,Human_Splice_Rec_480140,Human_Splice_Rec_480141,Human_Splice_Rec_480162,Human_Splice_Rec_480163,Human_Splice_Rec_480183 RMVar_hsa_circ_79285,RMVar_hsa_circ_221106,RMVar_hsa_circ_36464,RMVar_hsa_circ_46541 113359 RMVar_ID_113359 Human_SNP_ID_847361074 m1A Human chr3 + 155988495 155988495 155988495 AAAAAAGAAAAACCTGCTCCCTTCGCTCTGCTAGAAGCTGGAGGGTGCTAGGCCCCTGTGTAGTA AAAAAAGAAAAACCTGCTCCCTTCGCTCTGCTGGAAGCTGGAGGGTGCTAGGCCCCTGTGTAGTA A G lnc-GMPS-2 RNACentral:URS00008B367D lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1166371577 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 113360 RMVar_ID_113360 Human_SNP_ID_847371045 m1A Human chr3 + 47870913 47870913 47870913 CAGGAGCAGAAGTATTGGTGGCCAGGCGGCTGAGCCGGGGGGTGGTGGAGCTGGGTTTGGCCGAG CAGGAGCAGAAGTATTGGTGGCCAGGCGGCTGTGCCGGGGGGTGGTGGAGCTGGGTTTGGCCGAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:47870868..47871042;chr3:47870867..47871046 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 6 kidney 113361 RMVar_ID_113361 Human_SNP_ID_847377797 m1A Human chr3 - 48432802 48432802 48432802 GGGCCTGGTACATGCTGCTGGGCCAGGGCAGGACTCTGGGTCACAGGCAGGTAGTCCCCCGACCA GGGCCTGGTACATGCTGCTGGGCCAGGGCAGGCCTCTGGGTCACAGGCAGGTAGTCCCCCGACCA T G CCDC51 Ensembl:ENSG00000164051 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr3:48432704..48432803;chr3:48432753..48433884 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_27319224 RMVar_hsa_circ_123117,RMVar_hsa_circ_217850 113362 RMVar_ID_113362 Human_SNP_ID_847413528 m1A Human chr3 - 116644237 116644236 116644238 TTTTAAAAAAATAAAGTCCATACTTACACTTAAAAAAAAAAAAAAAAAAAGAATATACATAGAAC TTTTAAAAAAATAAAGTCCATACTTACACTT__AAAAAAAAAAAAAAAAAGAATATACATAGAAC TTT T LSAMP Ensembl:ENSG00000185565 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 32..33 33 LMS 1 - Human_RBP_ID_586394,Human_RBP_ID_22399349 113363 RMVar_ID_113363 Human_SNP_ID_847425365 m1A Human chr3 + 40466116 40466091 40466117 GGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGACATTACG GGGAGGCT__________________________GAGGTGGAGGTTGCAGTGAGCTGACATTACG TGAGGCGGGAGAATCGCTTGAACCCAG T RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 9..34 33 MELA 1 - 113364 RMVar_ID_113364 Human_SNP_ID_847456037 m1A Human chr3 - 51935402 51935395 51935403 CCGGGAGTGCTGTGTGACGGCTGGGGGCCGGGATGGGACTGTACGTGTGTGGAAGATCCCCGAGG CCGGGAGTGCTGTGTGACGGCTGGGGGCCGG________TGTACGTGTGTGGAAGATCCCCGAGG AGTCCCATC A RRP9 Ensembl:ENSG00000114767 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:51935352..51935419 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..39 33 BRCA 1 - Human_RBP_ID_247213 Human_Splice_Rec_435408,Human_Splice_Rec_435409 RMVar_hsa_circ_218550,RMVar_hsa_circ_81058,RMVar_hsa_circ_86850,RMVar_hsa_circ_112552,RMVar_hsa_circ_104490,RMVar_hsa_circ_83171,RMVar_hsa_circ_83929,RMVar_hsa_circ_218554,RMVar_hsa_circ_76657,RMVar_hsa_circ_80303,RMVar_hsa_circ_218556,RMVar_hsa_circ_218557,RMVar_hsa_circ_218555,RMVar_hsa_circ_218552,RMVar_hsa_circ_218553,RMVar_hsa_circ_218551,RMVar_hsa_circ_82206,RMVar_hsa_circ_93475,RMVar_hsa_circ_218562,RMVar_hsa_circ_218563 113365 RMVar_ID_113365 Human_SNP_ID_847461946 m1A Human chr3 + 10142047 10142047 10142047 CGGGCGGCCGCGGCCCGTGCTGCGCTCGGTGAACTCGCGCGAGCCCTCCCAGGTCATCTTCTGCA CGGGCGGCCGCGGCCCGTGCTGCGCTCGGTGAGCTCGCGCGAGCCCTCCCAGGTCATCTTCTGCA A G VHL Ensembl:ENSG00000134086 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:10141800..10142097 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney Human_RBP_ID_584597,Human_RBP_ID_1615076,Human_RBP_ID_9393296,Human_RBP_ID_14554137,Human_RBP_ID_18793174,Human_RBP_ID_23119954,Human_RBP_ID_27042012,Human_RBP_ID_27311217,Human_RBP_ID_27496404 113366 RMVar_ID_113366 Human_SNP_ID_847473023 m1A Human chr3 - 51993866 51993866 51993866 CGTATTGCCAAGGGGCTCAGGCTGTGCCGGCCAAAGGCCAAGGCCAAGGCCAAGGCCAAGGATCA CGTATTGCCAAGGGGCTCAGGCTGTGCCGGCCCAAGGCCAAGGCCAAGGCCAAGGCCAAGGATCA T G RPL29 Ensembl:ENSG00000162244 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_247519,Human_RBP_ID_9334200,Human_RBP_ID_17404644,Human_RBP_ID_17661150,Human_RBP_ID_18194612,Human_RBP_ID_22455929,Human_RBP_ID_22533911,Human_RBP_ID_23213517,Human_RBP_ID_26823919 Human_miRNA_ID_2217058 RMVar_hsa_circ_94206,RMVar_hsa_circ_103686,RMVar_hsa_circ_94743,RMVar_hsa_circ_218586,RMVar_hsa_circ_218587,RMVar_hsa_circ_218585 113367 RMVar_ID_113367 Human_SNP_ID_847539828 m1A Human chr3 - 184306121 184306121 184306121 GCATATGCACACACATCCACCAGTGTGTTGGCAAAACTGCGGAATGGCTCTGACACAACCTCCAG GCATATGCACACACATCCACCAGTGTGTTGGCCAAACTGCGGAATGGCTCTGACACAACCTCCAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:184306051..184306175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 testis seminoma 3 testis 113368 RMVar_ID_113368 Human_SNP_ID_847572243 m1A Human chr3 + 48970683 48970683 48970683 ACAGGAGCCTAGAGCTCGCCGAGTACAGTGCAATCGGTGCAACGAGGTCTTCTGGTAAGAGTGAG ACAGGAGCCTAGAGCTCGCCGAGTACAGTGCACTCGGTGCAACGAGGTCTTCTGGTAAGAGTGAG A C ARIH2 Ensembl:ENSG00000177479 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48970617..48970718 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_935243,Human_RBP_ID_3965168,Human_RBP_ID_8875009,Human_RBP_ID_9348533,Human_RBP_ID_14862525,Human_RBP_ID_19117419 Human_Splice_Rec_426420,Human_Splice_Rec_426421,Human_Splice_Rec_426446,Human_Splice_Rec_426470,Human_Splice_Rec_426471,Human_Splice_Rec_426494,Human_Splice_Rec_426495,Human_Splice_Rec_426516,Human_Splice_Rec_426517,Human_Splice_Rec_426542,Human_Splice_Rec_426624,Human_Splice_Rec_426625,Human_Splice_Rec_426660,Human_Splice_Rec_426666 RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_99714,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_52938,RMVar_hsa_circ_8152,RMVar_hsa_circ_56438,RMVar_hsa_circ_43608,RMVar_hsa_circ_42850,RMVar_hsa_circ_109511,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_218012 113369 RMVar_ID_113369 Human_SNP_ID_847580613 m1A Human chr3 - 101361850 101361850 101361850 TTATGATTTATTCCTTGTTAGATGTCATCTGAATTATGCCCATATAATCCTGTCATGGAGAACAT TTATGATTTATTCCTTGTTAGATGTCATCTGAGTTATGCCCATATAATCCTGTCATGGAGAACAT T C SENP7 Ensembl:ENSG00000138468 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7616677 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,mouth squamous_cell_carcinoma 13 head and neck Human_RBP_ID_9348877,Human_RBP_ID_26347065 Human_Splice_Rec_460152,Human_Splice_Rec_460192,Human_Splice_Rec_460236,Human_Splice_Rec_460280,Human_Splice_Rec_460336 GWAS_ID_13726,GWAS_ID_13727,GWAS_ID_13728,GWAS_ID_13729,GWAS_ID_13730,GWAS_ID_13731,GWAS_ID_13732,GWAS_ID_13733,GWAS_ID_13734,GWAS_ID_13735,GWAS_ID_13736,GWAS_ID_13737,GWAS_ID_13738,GWAS_ID_13739,GWAS_ID_13740,GWAS_ID_13741,GWAS_ID_13742,GWAS_ID_13743,GWAS_ID_13744,GWAS_ID_13745,GWAS_ID_13746,GWAS_ID_13747,GWAS_ID_13748,GWAS_ID_13749,GWAS_ID_13750,GWAS_ID_13751,GWAS_ID_13752,GWAS_ID_13753,GWAS_ID_13754,GWAS_ID_13755,GWAS_ID_13756,GWAS_ID_13757,GWAS_ID_13758,GWAS_ID_13759,GWAS_ID_13760,GWAS_ID_13761,GWAS_ID_13762,GWAS_ID_13763,GWAS_ID_13764,GWAS_ID_13765,GWAS_ID_13766,GWAS_ID_13767,GWAS_ID_13768,GWAS_ID_13769,GWAS_ID_13770,GWAS_ID_13771,GWAS_ID_13772,GWAS_ID_13773,GWAS_ID_13774,GWAS_ID_13775,GWAS_ID_13776,GWAS_ID_13777,GWAS_ID_13778,GWAS_ID_13779,GWAS_ID_13780,GWAS_ID_13781,GWAS_ID_13782,GWAS_ID_13783,GWAS_ID_13784,GWAS_ID_13785,GWAS_ID_13786,GWAS_ID_13787,GWAS_ID_13788,GWAS_ID_13789,GWAS_ID_13790,GWAS_ID_13791,GWAS_ID_13792,GWAS_ID_13793,GWAS_ID_13794,GWAS_ID_13795,GWAS_ID_13796,GWAS_ID_13797,GWAS_ID_13798,GWAS_ID_13799,GWAS_ID_13800,GWAS_ID_13801,GWAS_ID_13802,GWAS_ID_13803,GWAS_ID_13804,GWAS_ID_13805,GWAS_ID_13806,GWAS_ID_13807,GWAS_ID_13808,GWAS_ID_13809,GWAS_ID_13810,GWAS_ID_13811,GWAS_ID_13812,GWAS_ID_13813,GWAS_ID_13814,GWAS_ID_13815,GWAS_ID_13816,GWAS_ID_13817,GWAS_ID_13818,GWAS_ID_13819,GWAS_ID_13820,GWAS_ID_13821,GWAS_ID_13822,GWAS_ID_13823,GWAS_ID_13824,GWAS_ID_13825,GWAS_ID_13826,GWAS_ID_13827,GWAS_ID_13828,GWAS_ID_13829,GWAS_ID_13830,GWAS_ID_13831,GWAS_ID_13832,GWAS_ID_13833,GWAS_ID_13834,GWAS_ID_13835,GWAS_ID_13836,GWAS_ID_13837,GWAS_ID_13838,GWAS_ID_13839,GWAS_ID_13840,GWAS_ID_13841,GWAS_ID_13842,GWAS_ID_13843,GWAS_ID_13844,GWAS_ID_13845,GWAS_ID_13846,GWAS_ID_13847,GWAS_ID_13848,GWAS_ID_13849,GWAS_ID_13850,GWAS_ID_13851,GWAS_ID_13852,GWAS_ID_13853,GWAS_ID_13854,GWAS_ID_13855,GWAS_ID_13856,GWAS_ID_13857,GWAS_ID_13858,GWAS_ID_13859,GWAS_ID_13860,GWAS_ID_13861,GWAS_ID_13862,GWAS_ID_13863,GWAS_ID_13864,GWAS_ID_13865,GWAS_ID_13866,GWAS_ID_13867,GWAS_ID_13868,GWAS_ID_13869,GWAS_ID_13870,GWAS_ID_13871,GWAS_ID_13872,GWAS_ID_13873,GWAS_ID_13874,GWAS_ID_13875,GWAS_ID_13876,GWAS_ID_13877,GWAS_ID_13878,GWAS_ID_13879,GWAS_ID_13880,GWAS_ID_13881,GWAS_ID_13882,GWAS_ID_13883,GWAS_ID_13884,GWAS_ID_13885,GWAS_ID_13886,GWAS_ID_13887,GWAS_ID_13888,GWAS_ID_13889,GWAS_ID_13890,GWAS_ID_13891,GWAS_ID_13892,GWAS_ID_13893,GWAS_ID_13894,GWAS_ID_13895,GWAS_ID_13896,GWAS_ID_13897,GWAS_ID_13898,GWAS_ID_13899,GWAS_ID_13900,GWAS_ID_13901,GWAS_ID_13902,GWAS_ID_13903,GWAS_ID_13904,GWAS_ID_13905,GWAS_ID_13906,GWAS_ID_13907,GWAS_ID_13908,GWAS_ID_13909,GWAS_ID_13910,GWAS_ID_13911,GWAS_ID_13912,GWAS_ID_13913,GWAS_ID_13914,GWAS_ID_13915,GWAS_ID_13916,GWAS_ID_13917,GWAS_ID_13918,GWAS_ID_13919,GWAS_ID_13920,GWAS_ID_13921,GWAS_ID_13922,GWAS_ID_13923,GWAS_ID_13924,GWAS_ID_13925,GWAS_ID_13926,GWAS_ID_13927,GWAS_ID_13928,GWAS_ID_13929,GWAS_ID_13930,GWAS_ID_13931,GWAS_ID_13932,GWAS_ID_13933,GWAS_ID_13934,GWAS_ID_13935,GWAS_ID_13936,GWAS_ID_13937,GWAS_ID_13938,GWAS_ID_13939,GWAS_ID_13940,GWAS_ID_13941,GWAS_ID_13942,GWAS_ID_13943,GWAS_ID_13944,GWAS_ID_13945,GWAS_ID_13946,GWAS_ID_13947,GWAS_ID_13948,GWAS_ID_13949,GWAS_ID_13950,GWAS_ID_13951,GWAS_ID_13952,GWAS_ID_13953,GWAS_ID_13954,GWAS_ID_13955,GWAS_ID_13956,GWAS_ID_13957,GWAS_ID_13958,GWAS_ID_13959,GWAS_ID_13960,GWAS_ID_13961,GWAS_ID_13962,GWAS_ID_13963,GWAS_ID_13964,GWAS_ID_13965,GWAS_ID_13966,GWAS_ID_13967,GWAS_ID_13968,GWAS_ID_13969,GWAS_ID_13970,GWAS_ID_13971,GWAS_ID_13972,GWAS_ID_13973,GWAS_ID_13974,GWAS_ID_13975,GWAS_ID_13976,GWAS_ID_13977,GWAS_ID_13978,GWAS_ID_13979,GWAS_ID_13980,GWAS_ID_13981,GWAS_ID_13982,GWAS_ID_13983,GWAS_ID_13984,GWAS_ID_13985,GWAS_ID_13986,GWAS_ID_13987,GWAS_ID_13988,GWAS_ID_13989,GWAS_ID_13990,GWAS_ID_13991,GWAS_ID_13992 RMVar_hsa_circ_258,RMVar_hsa_circ_125297,RMVar_hsa_circ_220045,RMVar_hsa_circ_68576,RMVar_hsa_circ_12897,RMVar_hsa_circ_43436,RMVar_hsa_circ_334604,RMVar_hsa_circ_363248,RMVar_hsa_circ_220048,RMVar_hsa_circ_42476,RMVar_hsa_circ_306756,RMVar_hsa_circ_363657,RMVar_hsa_circ_11639,RMVar_hsa_circ_35031,RMVar_hsa_circ_14556,RMVar_hsa_circ_286579,RMVar_hsa_circ_5955,RMVar_hsa_circ_8059,RMVar_hsa_circ_11536,RMVar_hsa_circ_220050,RMVar_hsa_circ_220051,RMVar_hsa_circ_308699,RMVar_hsa_circ_38582,RMVar_hsa_circ_220052,RMVar_hsa_circ_1230,RMVar_hsa_circ_308456,RMVar_hsa_circ_323119,RMVar_hsa_circ_308384,RMVar_hsa_circ_220053,RMVar_hsa_circ_220054,RMVar_hsa_circ_220055 113370 RMVar_ID_113370 Human_SNP_ID_847601295 m1A Human chr3 + 50092156 50092156 50092156 GCGGAGGGACTCAGATTACAAAAGATCTAGTGATGATCGGAGGGGTGATAGATATGATGACTACC GCGGAGGGACTCAGATTACAAAAGATCTAGTGTTGATCGGAGGGGTGATAGATATGATGACTACC A T RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50092106..50092249 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 2 lung Human_RBP_ID_1628818,Human_RBP_ID_1964935,Human_RBP_ID_2789729,Human_RBP_ID_3710722,Human_RBP_ID_5206124,Human_RBP_ID_7206130,Human_RBP_ID_14875797,Human_RBP_ID_24008846,Human_RBP_ID_26346945 Human_Splice_Rec_432079,Human_Splice_Rec_432147,Human_Splice_Rec_432155,Human_Splice_Rec_432167,Human_Splice_Rec_432215,Human_Splice_Rec_432223,Human_Splice_Rec_432231,Human_Splice_Rec_432241,Human_Splice_Rec_432287,Human_Splice_Rec_432293,Human_Splice_Rec_432297 RMVar_hsa_circ_37410,RMVar_hsa_circ_87115,RMVar_hsa_circ_218326,RMVar_hsa_circ_48362,RMVar_hsa_circ_35608,RMVar_hsa_circ_218340,RMVar_hsa_circ_122540,RMVar_hsa_circ_86531,RMVar_hsa_circ_114466,RMVar_hsa_circ_353577,RMVar_hsa_circ_218339,RMVar_hsa_circ_356020,RMVar_hsa_circ_269516,RMVar_hsa_circ_57491,RMVar_hsa_circ_96641,RMVar_hsa_circ_218341,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_346293,RMVar_hsa_circ_93262,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346 113371 RMVar_ID_113371 Human_SNP_ID_847614931 m1A Human chr3 - 55467147 55467147 55467147 ACTGCAACTATTGCACCTCTCTATTTGAATTTACTGTGGACCATGTGTGGTGTCTCTATGCCCTT ACTGCAACTATTGCACCTCTCTATTTGAATTTGCTGTGGACCATGTGTGGTGTCTCTATGCCCTT T C WNT5A Ensembl:ENSG00000114251 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1829556 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_606309 Human_miRNA_ID_1081417,Human_miRNA_ID_2884291 Clinvar_Rec_483 GWAS_ID_10841,GWAS_ID_10842,GWAS_ID_10843,GWAS_ID_10844 RMVar_hsa_circ_218958,RMVar_hsa_circ_97111,RMVar_hsa_circ_99638,RMVar_hsa_circ_76776,RMVar_hsa_circ_218959,RMVar_hsa_circ_218957 113372 RMVar_ID_113372 Human_SNP_ID_847625722 m1A Human chr3 - 196075302 196075302 196075302 CCGGTTCAGCCTGGCTCGGCAAGTAGATGGCGATAACAGTCATGTGGAGATGAAACTTGCTGTAG CCGGTTCAGCCTGGCTCGGCAAGTAGATGGCGGTAACAGTCATGTGGAGATGAAACTTGCTGTAG T C TFRC Ensembl:ENSG00000072274 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196075251..196075395 26863196 MeRIP-seq:(Medium) rs769447421 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_66642,Human_RBP_ID_782868,Human_RBP_ID_938254,Human_RBP_ID_2774450,Human_RBP_ID_4756923,Human_RBP_ID_5530770,Human_RBP_ID_5602307,Human_RBP_ID_14761423,Human_RBP_ID_22092912,Human_RBP_ID_22418396,Human_RBP_ID_22456455 Human_Splice_Rec_529928,Human_Splice_Rec_529998,Human_Splice_Rec_530086,Human_Splice_Rec_530094 RMVar_hsa_circ_121595,RMVar_hsa_circ_223843,RMVar_hsa_circ_308948,RMVar_hsa_circ_4933,RMVar_hsa_circ_223854,RMVar_hsa_circ_341777,RMVar_hsa_circ_59092,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223865,RMVar_hsa_circ_223866,RMVar_hsa_circ_223867,RMVar_hsa_circ_329308,RMVar_hsa_circ_35376,RMVar_hsa_circ_297912,RMVar_hsa_circ_115479,RMVar_hsa_circ_223875,RMVar_hsa_circ_70073,RMVar_hsa_circ_325076,RMVar_hsa_circ_48394,RMVar_hsa_circ_223878,RMVar_hsa_circ_98087,RMVar_hsa_circ_279359,RMVar_hsa_circ_315825,RMVar_hsa_circ_223877,RMVar_hsa_circ_287545,RMVar_hsa_circ_223881,RMVar_hsa_circ_223879,RMVar_hsa_circ_223880,RMVar_hsa_circ_299304,RMVar_hsa_circ_320763,RMVar_hsa_circ_223882,RMVar_hsa_circ_223884,RMVar_hsa_circ_223883,RMVar_hsa_circ_311286,RMVar_hsa_circ_378331 113373 RMVar_ID_113373 Human_SNP_ID_847658725 m1A Human chr3 + 195694046 195694046 195694046 GAGGCAGACCTTGGTGTTTCCCAGGGTGTGGGACGTTGGGGGTAGTAAGGCTGGAGTGGGTAGAG GAGGCAGACCTTGGTGTTTCCCAGGGTGTGGGGCGTTGGGGGTAGTAAGGCTGGAGTGGGTAGAG A G MUC20-OT1 Ensembl:ENSG00000242086 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195693996..195694138 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_18954046 RMVar_hsa_circ_223821,RMVar_hsa_circ_223824,RMVar_hsa_circ_372521,RMVar_hsa_circ_223825,RMVar_hsa_circ_223823 113374 RMVar_ID_113374 Human_SNP_ID_847669402 m1A Human chr3 - 123148854 123148854 123148854 TCTGGGTGACGAGTCTCAGTTCTCCACCCCCGAGCCATCGGCTGTTCACACTCCACCTGAAGGAT TCTGGGTGACGAGTCTCAGTTCTCCACCCCCGGGCCATCGGCTGTTCACACTCCACCTGAAGGAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:123148853..123149316 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113375 RMVar_ID_113375 Human_SNP_ID_847670703 m1A Human chr3 - 185418562 185418562 185418562 CCAGTGCTGAGTCTTGGGGTACTGGCAGAGCTATGGCTCGAATTCCCAGAGTTCGAGGTGGTGGG CCAGTGCTGAGTCTTGGGGTACTGGCAGAGCTGTGGCTCGAATTCCCAGAGTTCGAGGTGGTGGG T C RPL4P4 Ensembl:ENSG00000229638 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879070985 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,STAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 13 haematopoietic and lymphoid tissue,breast Human_RBP_ID_1064073,Human_RBP_ID_27316202 Human_miRNA_ID_1857559,Human_miRNA_ID_1858345,Human_miRNA_ID_1886653 113376 RMVar_ID_113376 Human_SNP_ID_847688977 m1A Human chr3 - 171140498 171140498 171140498 TGTCTGCTTGTTGCCCCACAGCAACAAAGGCGAGAGAAGGAGCTGCGGAAGCAGCAGGAGAGGGA TGTCTGCTTGTTGCCCCACAGCAACAAAGGCGGGAGAAGGAGCTGCGGAAGCAGCAGGAGAGGGA T C TNIK Ensembl:ENSG00000154310 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:171140418..171140514 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 10 lung Human_RBP_ID_24547341 Human_Splice_Rec_506348,Human_Splice_Rec_506349,Human_Splice_Rec_506434,Human_Splice_Rec_506435,Human_Splice_Rec_506496,Human_Splice_Rec_506497,Human_Splice_Rec_506558,Human_Splice_Rec_506559,Human_Splice_Rec_506616,Human_Splice_Rec_506617,Human_Splice_Rec_506678,Human_Splice_Rec_506679,Human_Splice_Rec_506738,Human_Splice_Rec_506739,Human_Splice_Rec_506800,Human_Splice_Rec_506801 RMVar_hsa_circ_222652,RMVar_hsa_circ_79298,RMVar_hsa_circ_86580,RMVar_hsa_circ_222653,RMVar_hsa_circ_341823,RMVar_hsa_circ_367319,RMVar_hsa_circ_115106,RMVar_hsa_circ_104825,RMVar_hsa_circ_45519,RMVar_hsa_circ_342628,RMVar_hsa_circ_222655,RMVar_hsa_circ_278456,RMVar_hsa_circ_222656,RMVar_hsa_circ_222657 113377 RMVar_ID_113377 Human_SNP_ID_847699846 m1A Human chr3 - 52402676 52402665 52402676 GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTACAGATTGATGACCAGAGAAGGACCCACAACTACG GCTCCAGTGCTCTCAGTCTTCTTCTCTCCTAC___________CAGAGAAGGACCCACAACTACG GGTCATCAATCT G BAP1 Ensembl:ENSG00000163930 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402626..52402675 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..43 33 RECA 1 - Human_Splice_Rec_437913,Human_Splice_Rec_437919,Human_Splice_Rec_437951,Human_Splice_Rec_437959,Human_Splice_Rec_437965 113378 RMVar_ID_113378 Human_SNP_ID_847705639 m1A Human chr3 + 49174779 49174779 49174779 CGCCAGGGCAAGCTCCCGGTGACTGCTTTTGAAGCCTTTGATCTGGAGGCCCGTACATGGACCCG CGCCAGGGCAAGCTCCCGGTGACTGCTTTTGACGCCTTTGATCTGGAGGCCCGTACATGGACCCG A C KLHDC8B Ensembl:ENSG00000185909 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:49174743..49174940 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_604140 Human_Splice_Rec_428638,Human_Splice_Rec_428646,Human_Splice_Rec_428652,Human_Splice_Rec_428654 RMVar_hsa_circ_104345,RMVar_hsa_circ_218121 113379 RMVar_ID_113379 Human_SNP_ID_847705670 m1A Human chr3 + 42664371 42664371 42664371 GCGACGTGTGTGGCCAGCGCTTCCGCTTCTCCAACATGCTCAAGGCCCACAAGGAGAAGTGCTTC GCGACGTGTGTGGCCAGCGCTTCCGCTTCTCCGACATGCTCAAGGCCCACAAGGAGAAGTGCTTC A G ZBTB47 Ensembl:ENSG00000114853 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:42664321..42664468 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113380 RMVar_ID_113380 Human_SNP_ID_847713399 m1A Human chr3 + 139344110 139344110 139344110 CCGGGCGTGGAACGGGTCTGTTTCCGGGCTCGAATCCAGCCCTGGCACGGTGGCCTGCTCCAACC CCGGGCGTGGAACGGGTCTGTTTCCGGGCTCGTATCCAGCCCTGGCACGGTGGCCTGCTCCAACC A T MRPS22 Ensembl:ENSG00000175110 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:139344059..139344142 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8875637,Human_RBP_ID_22091895,Human_RBP_ID_22457011,Human_RBP_ID_26824144,Human_RBP_ID_27046397 Human_Splice_Rec_489671,Human_Splice_Rec_489693,Human_Splice_Rec_489707,Human_Splice_Rec_489723,Human_Splice_Rec_489737,Human_Splice_Rec_489749,Human_Splice_Rec_489755,Human_Splice_Rec_489765 113381 RMVar_ID_113381 Human_SNP_ID_847732005 m1A Human chr3 + 32727697 32727697 32727697 TAGGTAAAAAATTTTCAGGAAGACCCATGTGTACGTTACTAACCAATAAGAGATATGAGTTGCTG TAGGTAAAAAATTTTCAGGAAGACCCATGTGTTCGTTACTAACCAATAAGAGATATGAGTTGCTG A T CNOT10 Ensembl:ENSG00000182973 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11558687 Functional Loss SNV COSMIC 33..33 33 lymph_node acute_lymphoblastic_leukaemia,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_600193,Human_RBP_ID_1385672,Human_RBP_ID_22509456,Human_RBP_ID_23998041 Human_Splice_Rec_405712,Human_Splice_Rec_405746,Human_Splice_Rec_405780,Human_Splice_Rec_405834,Human_Splice_Rec_405874,Human_Splice_Rec_405902,Human_Splice_Rec_405912 GWAS_ID_13406,GWAS_ID_13407 RMVar_hsa_circ_304329,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_326007,RMVar_hsa_circ_272029,RMVar_hsa_circ_14283,RMVar_hsa_circ_216684,RMVar_hsa_circ_216685,RMVar_hsa_circ_216683,RMVar_hsa_circ_372874,RMVar_hsa_circ_216687,RMVar_hsa_circ_304200,RMVar_hsa_circ_309712,RMVar_hsa_circ_289810,RMVar_hsa_circ_8817,RMVar_hsa_circ_216689,RMVar_hsa_circ_216691,RMVar_hsa_circ_216690,RMVar_hsa_circ_216688,RMVar_hsa_circ_46950,RMVar_hsa_circ_312163,RMVar_hsa_circ_354902,RMVar_hsa_circ_65682,RMVar_hsa_circ_33057,RMVar_hsa_circ_43035,RMVar_hsa_circ_377129,RMVar_hsa_circ_39744,RMVar_hsa_circ_312378,RMVar_hsa_circ_216697,RMVar_hsa_circ_17871,RMVar_hsa_circ_216698 113382 RMVar_ID_113382 Human_SNP_ID_847734931 m1A Human chr3 + 13504525 13504523 13504525 TGTTCCGGATGGTCCGTGGCCGCCGGGTGCCCATCCTTATGGTGACCTCAGGCGGGTACCAGAAG TGTTCCGGATGGTCCGTGGCCGCCGGGTGCC__TCCTTATGGTGACCTCAGGCGGGTACCAGAAG CCA C HDAC11 Ensembl:ENSG00000163517 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13503232..13505428 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 GBM 1 - Human_Splice_Rec_396618,Human_Splice_Rec_396634,Human_Splice_Rec_396640,Human_Splice_Rec_396652,Human_Splice_Rec_396662,Human_Splice_Rec_396680,Human_Splice_Rec_396688,Human_Splice_Rec_396698,Human_Splice_Rec_396734,Human_Splice_Rec_396764,Human_Splice_Rec_396814 Human_miRNA_ID_88819 113383 RMVar_ID_113383 Human_SNP_ID_847749127 m1A Human chr3 - 134364416 134364412 134364416 AGGCGGACTTCTGGAGCCTGACTCTGCCAAAGAAAGGAAGCCATGGGGCGGGTTTCTGGGAGCTT AGGCGGACTTCTGGAGCCTGACTCTGCCAAAG____GAAGCCATGGGGCGGGTTTCTGGGAGCTT CCTTT C AMOTL2 Ensembl:ENSG00000114019 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134364414..134364720 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..36 33 CHOL 1 - RMVar_hsa_circ_99655,RMVar_hsa_circ_51792,RMVar_hsa_circ_109867,RMVar_hsa_circ_221494,RMVar_hsa_circ_221495 113384 RMVar_ID_113384 Human_SNP_ID_847800652 m1A Human chr3 - 186784953 186784952 186784953 GAGCTTGAGCAATCACATCATACCCTAAAAAAAGTAGGATACACATTTACCGATCCCACATCAAA GAGCTTGAGCAATCACATCATACCCTAAAAAA_GTAGGATACACATTTACCGATCCCACATCAAA CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186784951..186785164 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 CHOL 1 - 113385 RMVar_ID_113385 Human_SNP_ID_847801687 m1A Human chr3 + 49375525 49375525 49375525 CCTCTGGGAACTGGTCCTTGCTGAAGACTATGAGCAAGCATGTCTTTCCACAGGCTCCATCACCA CCTCTGGGAACTGGTCCTTGCTGAAGACTATGTGCAAGCATGTCTTTCCACAGGCTCCATCACCA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49375476..49375600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 3 haematopoietic and lymphoid tissue 113386 RMVar_ID_113386 Human_SNP_ID_847801761 m1A Human chr3 + 49375525 49375525 49375525 CCTCTGGGAACTGGTCCTTGCTGAAGACTATGAGCAAGCATGTCTTTCCACAGGCTCCATCACCA CCTCTGGGAACTGGTCCTTGCTGAAGACTATGCGCAAGCATGTCTTTCCACAGGCTCCATCACCA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49375476..49375600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma,stomach adenocarcinoma,stomach diffuse_adenocarcinoma,gastroesophageal_junction adenocarcinoma 19 stomach,prostate 113387 RMVar_ID_113387 Human_SNP_ID_847801765 m1A Human chr3 + 49375525 49375525 49375525 CCTCTGGGAACTGGTCCTTGCTGAAGACTATGAGCAAGCATGTCTTTCCACAGGCTCCATCACCA CCTCTGGGAACTGGTCCTTGCTGAAGACTATGGGCAAGCATGTCTTTCCACAGGCTCCATCACCA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49375476..49375600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 113388 RMVar_ID_113388 Human_SNP_ID_847807928 m1A Human chr3 - 48968568 48968568 48968568 GGAAGCAATGGAAACACAAAGTCCTCTGGTGTACGGAGTGGACAGTCCTGAGCCATGCAAGAGAC GGAAGCAATGGAAACACAAAGTCCTCTGGTGTGCGGAGTGGACAGTCCTGAGCCATGCAAGAGAC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48968526..48968675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113389 RMVar_ID_113389 Human_SNP_ID_847809328 m1A Human chr3 - 123584997 123584997 123584997 ACATGGCGGCAGTGGCGGCGACTGCAGCAGCGAAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGG ACATGGCGGCAGTGGCGGCGACTGCAGCAGCGGAGGGGAATGGGGGCGGCGGTGGCAGGGCCGGG T C HACD2 Ensembl:ENSG00000206527 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:123584514..123585075;chr3:123584425..123585075;chr3:123582226..123585075 26863196 MeRIP-seq:(Medium) rs751944112 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_247966,Human_RBP_ID_784249,Human_RBP_ID_4756668,Human_RBP_ID_20971418,Human_RBP_ID_22456103,Human_RBP_ID_24547569 RMVar_hsa_circ_121672,RMVar_hsa_circ_220744,RMVar_hsa_circ_125749,RMVar_hsa_circ_220750 113390 RMVar_ID_113390 Human_SNP_ID_847829073 m1A Human chr3 - 195908969 195908969 195908969 AAGTTCCGGCGAACTGGGGGAGCGGCAGTGGGAGAGCGTCGGGCGGGAGGCGGTGGTCCTGGGAG AAGTTCCGGCGAACTGGGGGAGCGGCAGTGGGGGAGCGTCGGGCGGGAGGCGGTGGTCCTGGGAG T C TNK2 Ensembl:ENSG00000061938 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:195908854..195909743 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_3721062,Human_RBP_ID_5325398,Human_RBP_ID_8124996,Human_RBP_ID_8209560,Human_RBP_ID_8236146,Human_RBP_ID_8729873,Human_RBP_ID_9434771,Human_RBP_ID_18954062,Human_RBP_ID_22725669 Human_miRNA_ID_2867362,Human_miRNA_ID_2867363 RMVar_hsa_circ_100106,RMVar_hsa_circ_223832,RMVar_hsa_circ_223834,RMVar_hsa_circ_126871 113391 RMVar_ID_113391 Human_SNP_ID_847836865 m1A Human chr3 + 13358314 13358314 13358314 AGGCGCGAGGGTGAGCCTGGACGGTGGGGCGCAGACGAACTTCACCACGGCAGGCTCCACCGCAG AGGCGCGAGGGTGAGCCTGGACGGTGGGGCGCGGACGAACTTCACCACGGCAGGCTCCACCGCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:13358201..13358427 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine 113392 RMVar_ID_113392 Human_SNP_ID_847870604 m1A Human chr3 + 184324926 184324926 184324926 GCCTGAAGGAAGAGCTGGAAGAGGCTCGGGACATAGCCCGGCGGCGCTCTTTAGGGAATATCAAG GCCTGAAGGAAGAGCTGGAAGAGGCTCGGGACGTAGCCCGGCGGCGCTCTTTAGGGAATATCAAG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184324872..184325032 26863196 MeRIP-seq:(Medium) rs373331022 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 15 lung Human_RBP_ID_247259,Human_RBP_ID_4733619,Human_RBP_ID_5447304,Human_RBP_ID_7167787,Human_RBP_ID_8870201,Human_RBP_ID_9261206,Human_RBP_ID_9303126,Human_RBP_ID_9394358,Human_RBP_ID_14745282,Human_RBP_ID_17703454,Human_RBP_ID_18001240,Human_RBP_ID_23026778,Human_RBP_ID_26347502 Human_Splice_Rec_516698,Human_Splice_Rec_516762,Human_Splice_Rec_516820,Human_Splice_Rec_516882,Human_Splice_Rec_517010,Human_Splice_Rec_517070,Human_Splice_Rec_517104,Human_Splice_Rec_517140,Human_Splice_Rec_517196,Human_Splice_Rec_517292,Human_Splice_Rec_517354,Human_Splice_Rec_517416,Human_Splice_Rec_517484,Human_Splice_Rec_517538,Human_Splice_Rec_517566,Human_Splice_Rec_517622,Human_Splice_Rec_517688 Human_miRNA_ID_2442815,Human_miRNA_ID_2442816 RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_105927,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372,RMVar_hsa_circ_54287,RMVar_hsa_circ_107668,RMVar_hsa_circ_223373,RMVar_hsa_circ_223374,RMVar_hsa_circ_309763,RMVar_hsa_circ_351209 113393 RMVar_ID_113393 Human_SNP_ID_847896680 m1A Human chr3 + 196077118 196077118 196077118 GCTTGATCCATCATTCTGAACTGCCACACAGAAGAACCTAGGTATCAGAATAGAGAATTATTGAG GCTTGATCCATCATTCTGAACTGCCACACAGACGAACCTAGGTATCAGAATAGAGAATTATTGAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:196077051..196077125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113394 RMVar_ID_113394 Human_SNP_ID_847898090 m1A Human chr3 - 185417702 185417702 185417702 CTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCAGCACTACCAGCCAAATCAGATGAAAAGGCGGC CTCCGGGTGGATAAGGCAGCTGCTGCAGCAGCGGCACTACCAGCCAAATCAGATGAAAAGGCGGC T C RPL4P4 Ensembl:ENSG00000229638 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879195525 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_miRNA_ID_1885991 113395 RMVar_ID_113395 Human_SNP_ID_847900424 m1A Human chr3 + 50118456 50118454 50118456 GCCATGTTTGCCCGGTTCACTGAGATGGAGTGAGAGAGAGAGAGAGAGAGAGATGACAAGGAGCA GCCATGTTTGCCCGGTTCACTGAGATGGAGT__GAGAGAGAGAGAGAGAGAGATGACAAGGAGCA TGA T RBM5 Ensembl:ENSG00000003756 Protein coding stop codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:50118405..50118508 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 PEME 2 - Human_RBP_ID_604511,Human_RBP_ID_782646,Human_RBP_ID_2789792,Human_RBP_ID_4747317,Human_RBP_ID_5530479,Human_RBP_ID_8575302,Human_RBP_ID_14876972,Human_RBP_ID_18007595,Human_RBP_ID_24008965,Human_RBP_ID_24383026,Human_RBP_ID_26346952,Human_RBP_ID_27822302 RMVar_hsa_circ_99731,RMVar_hsa_circ_218388 113396 RMVar_ID_113396 Human_SNP_ID_847942332 m1A Human chr3 - 187721823 187721823 187721823 TGAGAAAGAGCACTTAAGAGAATATTTTAAGTATTGCATCTGTATAAGTAAGAAAATATTTTGTC TGAGAAAGAGCACTTAAGAGAATATTTTAAGTTTTGCATCTGTATAAGTAAGAAAATATTTTGTC T A BCL6 Ensembl:ENSG00000113916 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs115678349 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8949904,Human_RBP_ID_23991033 Human_miRNA_ID_532903,Human_miRNA_ID_539109,Human_miRNA_ID_1255636 113397 RMVar_ID_113397 Human_SNP_ID_847954482 m1A Human chr3 + 52247790 52247790 52247790 AGGGAAAGCTGTACATGGCCAATGCTGGGGATAGCAGGTGAGTCACCCCTTGGAGGGTGGGCAAG AGGGAAAGCTGTACATGGCCAATGCTGGGGATCGCAGGTGAGTCACCCCTTGGAGGGTGGGCAAG A C PPM1M Ensembl:ENSG00000164088 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52247741..52248249 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_282813 Human_Splice_Rec_437247,Human_Splice_Rec_437263,Human_Splice_Rec_437277,Human_Splice_Rec_437291,Human_Splice_Rec_437305,Human_Splice_Rec_437321,Human_Splice_Rec_437331 RMVar_hsa_circ_76852,RMVar_hsa_circ_85701,RMVar_hsa_circ_218614,RMVar_hsa_circ_93053,RMVar_hsa_circ_218615,RMVar_hsa_circ_218616 113398 RMVar_ID_113398 Human_SNP_ID_847972220 m1A Human chr3 - 146160977 146160977 146160977 GCGGCCCTCGAGGGCCGAATATGGGGGGATGCACGGTGAAGCCTCAGCTGCTGCTCCTGGCGCTC GCGGCCCTCGAGGGCCGAATATGGGGGGATGCGCGGTGAAGCCTCAGCTGCTGCTCCTGGCGCTC T C PLOD2 Ensembl:ENSG00000152952 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:146160926..146163603 26863196 MeRIP-seq:(Medium) rs1355371514 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_784995,Human_RBP_ID_4756776,Human_RBP_ID_5473828 Human_Splice_Rec_493499,Human_Splice_Rec_493537,Human_Splice_Rec_493639 113399 RMVar_ID_113399 Human_SNP_ID_848028406 m1A Human chr3 + 49675943 49675943 49675943 GCTCAAGAGCTTCAACCTGTCAGCGCTGGAGAAACATGGGCCTGTTTATGAGGATGGTGAGGCAT GCTCAAGAGCTTCAACCTGTCAGCGCTGGAGAGACATGGGCCTGTTTATGAGGATGGTGAGGCAT A G APEH Ensembl:ENSG00000164062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49675870..49675958 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19010348 Human_Splice_Rec_430012,Human_Splice_Rec_430013,Human_Splice_Rec_430026,Human_Splice_Rec_430027,Human_Splice_Rec_430036,Human_Splice_Rec_430037,Human_Splice_Rec_430074,Human_Splice_Rec_430075,Human_Splice_Rec_430092,Human_Splice_Rec_430093,Human_Splice_Rec_430100,Human_Splice_Rec_430101,Human_Splice_Rec_430122,Human_Splice_Rec_430123,Human_Splice_Rec_430162,Human_Splice_Rec_430163,Human_Splice_Rec_430176,Human_Splice_Rec_430177,Human_Splice_Rec_430186,Human_Splice_Rec_430187,Human_Splice_Rec_430206,Human_Splice_Rec_430212,Human_Splice_Rec_430213,Human_Splice_Rec_430222,Human_Splice_Rec_430223 RMVar_hsa_circ_11861,RMVar_hsa_circ_49672,RMVar_hsa_circ_77835,RMVar_hsa_circ_111819,RMVar_hsa_circ_120196,RMVar_hsa_circ_95140,RMVar_hsa_circ_123247,RMVar_hsa_circ_218188,RMVar_hsa_circ_218189,RMVar_hsa_circ_218190,RMVar_hsa_circ_218187,RMVar_hsa_circ_108031,RMVar_hsa_circ_121880,RMVar_hsa_circ_91925,RMVar_hsa_circ_103743,RMVar_hsa_circ_83852,RMVar_hsa_circ_218191,RMVar_hsa_circ_218193,RMVar_hsa_circ_218194,RMVar_hsa_circ_218192,RMVar_hsa_circ_112521,RMVar_hsa_circ_117751,RMVar_hsa_circ_218195,RMVar_hsa_circ_218196,RMVar_hsa_circ_120410,RMVar_hsa_circ_111423,RMVar_hsa_circ_87033,RMVar_hsa_circ_81893,RMVar_hsa_circ_52285,RMVar_hsa_circ_218198,RMVar_hsa_circ_218200,RMVar_hsa_circ_218202,RMVar_hsa_circ_218201,RMVar_hsa_circ_218199,RMVar_hsa_circ_122762,RMVar_hsa_circ_218197,RMVar_hsa_circ_79505,RMVar_hsa_circ_218204,RMVar_hsa_circ_218205 113400 RMVar_ID_113400 Human_SNP_ID_848036574 m1A Human chr3 + 108191604 108191604 108191604 TTCTAGGCTCCATTCTGCAGCATCTGTTGTGGATTCCAAAATATCTTCTTGTTTGGCAGTCTCGT TTCTAGGCTCCATTCTGCAGCATCTGTTGTGGTTTCCAAAATATCTTCTTGTTTGGCAGTCTCGT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:108191529..108213814 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 113401 RMVar_ID_113401 Human_SNP_ID_848039318 m1A Human chr3 + 4983204 4983204 4983204 ACACAGACAGTGGCTATGGAGGAGAATCGGAGAAGGGCGACTTGCGCAGTGAGCAGCCGTGCTTC ACACAGACAGTGGCTATGGAGGAGAATCGGAGTAGGGCGACTTGCGCAGTGAGCAGCCGTGCTTC A T BHLHE40 Ensembl:ENSG00000134107 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:4983102..4983451 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_67536,Human_RBP_ID_783336,Human_RBP_ID_836070,Human_RBP_ID_8875373,Human_RBP_ID_9302107,Human_RBP_ID_19011343,Human_RBP_ID_22091376,Human_RBP_ID_22455308,Human_RBP_ID_27503258 Human_miRNA_ID_1967657 RMVar_hsa_circ_93229,RMVar_hsa_circ_215544 113402 RMVar_ID_113402 Human_SNP_ID_848047346 m1A Human chr3 + 130746630 130746630 130746630 GACCCCTCCAGCCCCCTAACCTGCCCTGGGGGACATGCGTTCCCGGGCCTCGTCTTCCTCTAGCG GACCCCTCCAGCCCCCTAACCTGCCCTGGGGGCCATGCGTTCCCGGGCCTCGTCTTCCTCTAGCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:130746579..130746786 26863196 MeRIP-seq:(Medium) rs2293179 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5505511,Human_RBP_ID_7243171 GWAS_ID_13145,GWAS_ID_13146 113403 RMVar_ID_113403 Human_SNP_ID_848069992 m1A Human chr3 - 17161098 17161098 17161098 CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCAGTCTGCTCCCCACTGGTGTTCTCAGATCCACT CTCAGAAGCACCTCTGGGAAAAGCCAGGCCCCGGTCTGCTCCCCACTGGTGTTCTCAGATCCACT T C TBC1D5 Ensembl:ENSG00000131374 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:17161050..17161151 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_27499929 Human_miRNA_ID_2366170,Human_miRNA_ID_2366171,Human_miRNA_ID_2724956,Human_miRNA_ID_2724957,Human_miRNA_ID_3013978,Human_miRNA_ID_3013979 RMVar_hsa_circ_109601,RMVar_hsa_circ_118271,RMVar_hsa_circ_115931,RMVar_hsa_circ_216297,RMVar_hsa_circ_216299,RMVar_hsa_circ_85797,RMVar_hsa_circ_216298,RMVar_hsa_circ_216296 113404 RMVar_ID_113404 Human_SNP_ID_848100535 m1A Human chr3 + 129605314 129605314 129605314 CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCGGGTGTACCTGGATGTTGAGCTTGCG CCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCGGGTGTACCTGGATGTTGAGCTTGCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:129605181..129605396;chr3:129605180..129605397 26863196 MeRIP-seq:(Medium) rs1411597579 Functional Loss SNV ICGC 33..33 33 STAD 1 - 113405 RMVar_ID_113405 Human_SNP_ID_848104838 m1A Human chr3 - 101457475 101457475 101457475 AACAACCCTAAAGTTCAGGCATCTCTGGCAGCAAACACTTTCACCATTACAGGCCATGCCGAGAC AACAACCCTAAAGTTCAGGCATCTCTGGCAGCGAACACTTTCACCATTACAGGCCATGCCGAGAC T C AC110994.3,SENP7 Ensembl:ENSG00000282978,Ensembl:ENSG00000138468 Pseudogene,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879161338 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue RMVar_hsa_circ_363248,RMVar_hsa_circ_43423,RMVar_hsa_circ_220062,RMVar_hsa_circ_66458,RMVar_hsa_circ_311615,RMVar_hsa_circ_220060,RMVar_hsa_circ_294147 113406 RMVar_ID_113406 Human_SNP_ID_848131842 m1A Human chr3 + 47663744 47663744 47663744 GAGTTTCAAGGAAAAGTTCCTTCACAAGACCCACGAGAACCCGGTGGTACCCATAGGTTGCCTGG GAGTTTCAAGGAAAAGTTCCTTCACAAGACCCGCGAGAACCCGGTGGTACCCATAGGTTGCCTGG A G AC130472.1 Ensembl:ENSG00000235695 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1286852520 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1835569 113407 RMVar_ID_113407 Human_SNP_ID_848139471 m1A Human chr3 + 184380405 184380405 184380405 CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCAGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA CTCGGCTCCCGGCCGGCCCGCGGCGCCGGCCCCGAGCCCCCCGTGCTGCCCATCCGTTCTGAGAA A C CHRD Ensembl:ENSG00000090539 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1920128 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,liver hepatocellular_carcinoma 13 liver,head and neck Human_RBP_ID_5133530,Human_RBP_ID_9395775,Human_RBP_ID_18471739 Human_Splice_Rec_518553,Human_Splice_Rec_518569,Human_Splice_Rec_518613,Human_Splice_Rec_518659,Human_Splice_Rec_518703,Human_Splice_Rec_518733,Human_Splice_Rec_518777,Human_Splice_Rec_518819,Human_Splice_Rec_518857,Human_Splice_Rec_518859 113408 RMVar_ID_113408 Human_SNP_ID_848258297 m1A Human chr3 + 196074041 196074041 196074041 CTGCAGGGAAGTCCTCTCCTGGCTCCTCCCTCACTGGAGACTCGGTTCCTGCCAGTCTCTCACAC CTGCAGGGAAGTCCTCTCCTGGCTCCTCCCTCGCTGGAGACTCGGTTCCTGCCAGTCTCTCACAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:196073990..196074070 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - 113409 RMVar_ID_113409 Human_SNP_ID_848267658 m1A Human chr3 + 127604947 127604947 127604947 GGAGCGCCCTGCCCGCAAGCGCCGCCAGGTGGAGCGGGCCACGGAGGACGGCGAGGAGGACGAGG GGAGCGCCCTGCCCGCAAGCGCCGCCAGGTGGGGCGGGCCACGGAGGACGGCGAGGAGGACGAGG A G MCM2 Ensembl:ENSG00000073111 Protein coding 3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:127604737..127605075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_247075,Human_RBP_ID_3965428,Human_RBP_ID_4720909,Human_RBP_ID_7117071,Human_RBP_ID_8867624,Human_RBP_ID_9302451,Human_RBP_ID_9334254,Human_RBP_ID_9394039,Human_RBP_ID_23026759,Human_RBP_ID_26348320 Human_Splice_Rec_479078,Human_Splice_Rec_479108,Human_Splice_Rec_479142,Human_Splice_Rec_479168 Human_miRNA_ID_2027023,Human_miRNA_ID_2464660 RMVar_hsa_circ_52356,RMVar_hsa_circ_120433,RMVar_hsa_circ_52677,RMVar_hsa_circ_97888,RMVar_hsa_circ_220995,RMVar_hsa_circ_220996,RMVar_hsa_circ_105151,RMVar_hsa_circ_40863,RMVar_hsa_circ_101595,RMVar_hsa_circ_220997,RMVar_hsa_circ_41570,RMVar_hsa_circ_220998 113410 RMVar_ID_113410 Human_SNP_ID_848297986 m1A Human chr3 - 15427681 15427681 15427681 GCTGGCGTCTGGGAGGACTGTGCTTCCGGGCCACCGCTCTGGAAGACAAGGAGAGCCGAGCCGGC GCTGGCGTCTGGGAGGACTGTGCTTCCGGGCCGCCGCTCTGGAAGACAAGGAGAGCCGAGCCGGC T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:15427634..15427760 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 113411 RMVar_ID_113411 Human_SNP_ID_848301619 m1A Human chr3 + 187743781 187743781 187743781 CCCCCGGAGCTCAGCCGATTTCTGAGGCTCCAACTCTACCCACTCCCTCCCCGGGCCGCCGCCGC CCCCCGGAGCTCAGCCGATTTCTGAGGCTCCACCTCTACCCACTCCCTCCCCGGGCCGCCGCCGC A C AC072022.2 Ensembl:ENSG00000285938 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:187743779..187743940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 MALY,haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 3 haematopoietic and lymphoid tissue 113412 RMVar_ID_113412 Human_SNP_ID_848307952 m1A Human chr3 - 47867340 47867340 47867340 TTTGTGTTGTTTTTTCTATTTTCTAACACTCCAGGTCCAGATAGTCTCCAAAAAAGTGAGCTACA TTTGTGTTGTTTTTTCTATTTTCTAACACTCCGGGTCCAGATAGTCTCCAAAAAAGTGAGCTACA T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:47867305..47867378 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_7202230 Human_Splice_Rec_423333,Human_Splice_Rec_423371,Human_Splice_Rec_423407,Human_Splice_Rec_423423,Human_Splice_Rec_423439 RMVar_hsa_circ_114442,RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_42607,RMVar_hsa_circ_81267,RMVar_hsa_circ_217785,RMVar_hsa_circ_274956,RMVar_hsa_circ_98216,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,RMVar_hsa_circ_74012,RMVar_hsa_circ_217786,RMVar_hsa_circ_365906,RMVar_hsa_circ_90786,RMVar_hsa_circ_217790,RMVar_hsa_circ_217788,RMVar_hsa_circ_217789,RMVar_hsa_circ_325035,RMVar_hsa_circ_325660,RMVar_hsa_circ_271350 113413 RMVar_ID_113413 Human_SNP_ID_848366643 m1A Human chr3 - 62372554 62372554 62372554 TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGAGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG TGGAAAAGCAGCCTCCGGGCGGGCGGCGGCGGCGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGG T G FEZF2 Ensembl:ENSG00000153266 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr3:62372440..62372556 26863196 MeRIP-seq:(Medium) rs201688981 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_5208191,Human_RBP_ID_18464653 113414 RMVar_ID_113414 Human_SNP_ID_848388322 m1A Human chr3 - 32238843 32238843 32238843 GGGAGCGCGGCCCGCGCGGGGCAGGAGGTGCGAGGGGGGCGCCCGCCGGGGGCTGTCCAGGCGCG GGGAGCGCGGCCCGCGCGGGGCAGGAGGTGCGGGGGGGGCGCCCGCCGGGGGCTGTCCAGGCGCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:32238743..32238875 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - 113415 RMVar_ID_113415 Human_SNP_ID_848415585 m1A Human chr3 - 111979099 111979099 111979099 GGACGGCTGCCCAGCCCCAGCTCCGACAAGGTACCCAGGCCGCCACAGCTGCCAAGCGCGCAACC GGACGGCTGCCCAGCCCCAGCTCCGACAAGGTCCCCAGGCCGCCACAGCTGCCAAGCGCGCAACC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:111979051..111979170 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113416 RMVar_ID_113416 Human_SNP_ID_848502387 m1A Human chr3 - 99818024 99818024 99818024 ACAGAGTGGGTACCTGGGCTGCTGCCTGCTCCAGTCGGCTGGTTCTCCCACCACTCGTCTCCGAG ACAGAGTGGGTACCTGGGCTGCTGCCTGCTCCGGTCGGCTGGTTCTCCCACCACTCGTCTCCGAG T C HP09053 RNACentral:URS000075B589 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr3:99817851..99818083;chr3:99817851..99818100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113417 RMVar_ID_113417 Human_SNP_ID_848527522 m1A Human chr3 - 37040274 37040274 37040274 CAGCTGATTTACCTAAGCTTGGTGGTGTTGAGAAGGTATAACTTGGTTTGATGCTGTGCCAAGGC CAGCTGATTTACCTAAGCTTGGTGGTGTTGAGGAGGTATAACTTGGTTTGATGCTGTGCCAAGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:37040224..37047584 32194978 MeRIP-seq:(Medium) rs768770694 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Clinvar_Rec_637 113418 RMVar_ID_113418 Human_SNP_ID_848622406 m1A Human chr3 + 143012301 143012301 143012301 ACCTAAGAGCCCAAGAAAACATAATTATAGGAATGAAAGTGCCCGTGAAAGCCTTTGTGATTCTC ACCTAAGAGCCCAAGAAAACATAATTATAGGAGTGAAAGTGCCCGTGAAAGCCTTTGTGATTCTC A G U2SURP Ensembl:ENSG00000163714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:143012251..143012325 26863196 MeRIP-seq:(Medium) rs1465944994 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_1951443,Human_RBP_ID_2753673,Human_RBP_ID_8561070,Human_RBP_ID_14657716,Human_RBP_ID_23974966,Human_RBP_ID_26347257 Human_Splice_Rec_493018,Human_Splice_Rec_493019,Human_Splice_Rec_493026,Human_Splice_Rec_493027,Human_Splice_Rec_493076,Human_Splice_Rec_493077,Human_Splice_Rec_493086,Human_Splice_Rec_493087,Human_Splice_Rec_493138,Human_Splice_Rec_493139,Human_Splice_Rec_493160,Human_Splice_Rec_493161,Human_Splice_Rec_493214,Human_Splice_Rec_493215,Human_Splice_Rec_493268,Human_Splice_Rec_493269,Human_Splice_Rec_493286,Human_Splice_Rec_493287,Human_Splice_Rec_493294,Human_Splice_Rec_493295,Human_Splice_Rec_493301 Human_miRNA_ID_2439425 RMVar_hsa_circ_32599,RMVar_hsa_circ_354873,RMVar_hsa_circ_366568,RMVar_hsa_circ_377475,RMVar_hsa_circ_73220,RMVar_hsa_circ_366991,RMVar_hsa_circ_356024,RMVar_hsa_circ_71890,RMVar_hsa_circ_327972,RMVar_hsa_circ_56230,RMVar_hsa_circ_222033 113419 RMVar_ID_113419 Human_SNP_ID_848625451 m1A Human chr3 + 49531817 49531817 49531817 AGAAGCCACGAGTATCCACACCAAAACCAGCAACGCCTTCAACTGACTCCACCACCACCACGACT AGAAGCCACGAGTATCCACACCAAAACCAGCAGCGCCTTCAACTGACTCCACCACCACCACGACT A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:49531769..49531940 26863196 MeRIP-seq:(Medium) rs149838438 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 6 lung Human_RBP_ID_1628593,Human_RBP_ID_17194907,Human_RBP_ID_17290505,Human_RBP_ID_17403808,Human_RBP_ID_18209901,Human_RBP_ID_27502979 Clinvar_Rec_476 113420 RMVar_ID_113420 Human_SNP_ID_848644775 m1A Human chr3 - 56683119 56683119 56683119 GGTCGGGAGCGCAGCCTGAGGCCACGGGGGGAAGGGGGTGGGTGGGCTGAGAGCAGCTCGGCGGC GGTCGGGAGCGCAGCCTGAGGCCACGGGGGGAGGGGGGTGGGTGGGCTGAGAGCAGCTCGGCGGC T C TASOR Ensembl:ENSG00000163946 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:56683069..56683227 26863196 MeRIP-seq:(Medium) rs1292714275 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4758141,Human_RBP_ID_5506715,Human_RBP_ID_9302359,Human_RBP_ID_9395237,Human_RBP_ID_22725768,Human_RBP_ID_27504189 113421 RMVar_ID_113421 Human_SNP_ID_848651239 m1A Human chr3 - 69024158 69024158 69024158 TGCTTCTCAGCTAGAAATTGGCAATCTAGAAAAAACTCGATCAATAATGGCTGAAGAACTAGTTA TGCTTCTCAGCTAGAAATTGGCAATCTAGAAACAACTCGATCAATAATGGCTGAAGAACTAGTTA T G TMF1 Ensembl:ENSG00000144747 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:69024109..69024311 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_2798731 Human_Splice_Rec_450890,Human_Splice_Rec_450918,Human_Splice_Rec_450950,Human_Splice_Rec_450980 RMVar_hsa_circ_219544 113422 RMVar_ID_113422 Human_SNP_ID_848675100 m1A Human chr3 + 197782055 197782052 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTT___AAAAAAAAAACGTATAAAATAATGCCCTGAAA TTTA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs75658829 Functional Loss DEL TCGA 31..33 33 COAD 1 - Human_RBP_ID_69843,Human_RBP_ID_598524 113423 RMVar_ID_113423 Human_SNP_ID_848679276 m1A Human chr3 - 52402810 52402808 52402811 GGCTGAGATTGCAAACTATGAGGCGTGCCTCAAGGAGGAGGTAGAGAAGAGGAAGAAGTTCAAGG GGCTGAGATTGCAAACTATGAGGCGTGCCTC___GAGGAGGTAGAGAAGAGGAAGAAGTTCAAGG CCTT C BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52402801..52402825 26863196 MeRIP-seq:(Medium) rs1226165465 Functional Loss DEL TCGA 32..34 33 MESO 1 - Human_RBP_ID_605389,Human_RBP_ID_1033814,Human_RBP_ID_17704363,Human_RBP_ID_18008232,Human_RBP_ID_19010554,Human_RBP_ID_19115716 Human_Splice_Rec_437910,Human_Splice_Rec_437911,Human_Splice_Rec_437917,Human_Splice_Rec_437948,Human_Splice_Rec_437949,Human_Splice_Rec_437957,Human_Splice_Rec_437963 Clinvar_Rec_479 113424 RMVar_ID_113424 Human_SNP_ID_848790125 m1A Human chr3 - 50089007 50089007 50089007 CCGCACTTACCCCAAGGAGAGACCGAAGCAGCAGTAGCGGTTCTGCGCCCCAGAACCTCCAACAA CCGCACTTACCCCAAGGAGAGACCGAAGCAGCTGTAGCGGTTCTGCGCCCCAGAACCTCCAACAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:50088957..50089881 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 113425 RMVar_ID_113425 Human_SNP_ID_848793992 m1A Human chr3 + 184321457 184321457 184321457 GCAGTCCTCTCTATTCCTGGGGACACTATGACAACTATACAAATGTCTGTAGAAGAATCAACCCC GCAGTCCTCTCTATTCCTGGGGACACTATGACGACTATACAAATGTCTGTAGAAGAATCAACCCC A G EIF4G1 Ensembl:ENSG00000114867 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:184321451..184321475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_67236,Human_RBP_ID_1623337,Human_RBP_ID_1957497,Human_RBP_ID_3699304,Human_RBP_ID_8567092,Human_RBP_ID_8870133,Human_RBP_ID_9261193,Human_RBP_ID_9394333,Human_RBP_ID_17289368,Human_RBP_ID_17402751,Human_RBP_ID_17518770,Human_RBP_ID_18001230,Human_RBP_ID_18336230,Human_RBP_ID_18803713,Human_RBP_ID_18954769,Human_RBP_ID_22092882,Human_RBP_ID_23020911,Human_RBP_ID_27316084,Human_RBP_ID_27500242 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371,RMVar_hsa_circ_88285,RMVar_hsa_circ_223372 113426 RMVar_ID_113426 Human_SNP_ID_848838000 m1A Human chr3 - 127629269 127629269 127629269 GAGCGCACTCACCCCCAACCAGCAGAAGCAGCAGCGGCGAAAGCAGCGGCGGCAGCCGGGCGGCC GAGCGCACTCACCCCCAACCAGCAGAAGCAGCGGCGGCGAAAGCAGCGGCGGCAGCCGGGCGGCC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:127629220..127629346 26863196 MeRIP-seq:(Medium) rs1212278376 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113427 RMVar_ID_113427 Human_SNP_ID_848853168 m1A Human chr3 - 12836135 12836135 12836135 TGGAAAGAGCTGCCCAACTGGCCATCAGAGTCACCAACCCCAATGCCAGGCTGCGCAGTGAAGAA TGGAAAGAGCTGCCCAACTGGCCATCAGAGTCGCCAACCCCAATGCCAGGCTGCGCAGTGAAGAA T C RPL32 Ensembl:ENSG00000144713 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:12836084..12836194 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_248321,Human_RBP_ID_588863,Human_RBP_ID_784472,Human_RBP_ID_1102658,Human_RBP_ID_1617517,Human_RBP_ID_1948888,Human_RBP_ID_3685679,Human_RBP_ID_4760752,Human_RBP_ID_8558294,Human_RBP_ID_9131843,Human_RBP_ID_14615209,Human_RBP_ID_18194484,Human_RBP_ID_18796553,Human_RBP_ID_26503371,Human_RBP_ID_26678286,Human_RBP_ID_26823586,Human_RBP_ID_27045083,Human_RBP_ID_27313099 Human_Splice_Rec_396266,Human_Splice_Rec_396272,Human_Splice_Rec_396278,Human_Splice_Rec_396284,Human_Splice_Rec_396288,Human_Splice_Rec_396294 113428 RMVar_ID_113428 Human_SNP_ID_848876823 m1A Human chr3 - 186783632 186783610 186783632 CCGCGACCGCCAACAGACTGCATACCTGTTATAATCCGCGGAGCCACCAGACATGATCCGAAAAA CCGCGACCGCCAACAGACTGCATACCTGTTAT______________________GATCCGAAAAA CATGTCTGGTGGCTCCGCGGATT C AC112907.3 Ensembl:ENSG00000263826 lincRNA exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:186783628..186783729 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..54 33 HNSC 1 - 113429 RMVar_ID_113429 Human_SNP_ID_848889811 m1A Human chr3 + 87227425 87227425 87227425 CCGACCTCCTCCTGCTGTCTCTCCGCTCCGCCACCCCGAACCCGCCAAGGTCCTGTCCTTTTCCT CCGACCTCCTCCTGCTGTCTCTCCGCTCCGCCCCCCCGAACCCGCCAAGGTCCTGTCCTTTTCCT A C CHMP2B Ensembl:ENSG00000083937 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO chr3:87227324..87227575;chr3:87227301..87227500;chr3:87227301..87240333 26863196,26863410 MeRIP-seq:(Medium) rs1032371345 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_608479,Human_RBP_ID_18954534 113430 RMVar_ID_113430 Human_SNP_ID_848901573 m1A Human chr3 - 49057373 49057373 49057373 GGCCACCGTGCTGGCCATTCCACAGGGCCAGCAGCAGAGTTATGTGTCTTTGAGGCCAGACTTAC GGCCACCGTGCTGGCCATTCCACAGGGCCAGCGGCAGAGTTATGTGTCTTTGAGGCCAGACTTAC T C QRICH1 Ensembl:ENSG00000198218 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49057226..49057427 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_604084,Human_RBP_ID_9302912,Human_RBP_ID_22605870 Human_miRNA_ID_2953362,Human_miRNA_ID_2957105 RMVar_hsa_circ_10931,RMVar_hsa_circ_54028,RMVar_hsa_circ_308831,RMVar_hsa_circ_316508,RMVar_hsa_circ_218053,RMVar_hsa_circ_218054,RMVar_hsa_circ_71815,RMVar_hsa_circ_336678,RMVar_hsa_circ_308718,RMVar_hsa_circ_310788,RMVar_hsa_circ_218057,RMVar_hsa_circ_218058 113431 RMVar_ID_113431 Human_SNP_ID_848904789 m1A Human chr3 + 33142944 33142944 33142944 CCACAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCTCTTTCTCACCTTTACACCTGTC CCACAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCTCTTTCTCACCTTTACACCTGTC A G CRTAP Ensembl:ENSG00000170275 Protein coding 3'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:33142801..33143025 26863410 MeRIP-seq:(Medium) rs1414037282 Functional Loss SNV COSMIC 33..33 33 colon tubular,large_intestine tubular 2 large intestine Human_RBP_ID_600363,Human_RBP_ID_17289985,Human_RBP_ID_17519700,Human_RBP_ID_18004462,Human_RBP_ID_18201596,Human_RBP_ID_18209866,Human_RBP_ID_20786491,Human_RBP_ID_27501171 Human_miRNA_ID_1062231,Human_miRNA_ID_2492433 RMVar_hsa_circ_88820,RMVar_hsa_circ_216733 113432 RMVar_ID_113432 Human_SNP_ID_848923449 m1A Human chr3 + 197782055 197782054 197782055 TCTTATTTTTATTTTTGAAGGTTTTTTTTTTTAAAAAAAAAAACGTATAAAATAATGCCCTGAAA TCTTATTTTTATTTTTGAAGGTTTTTTTTTTT_AAAAAAAAAACGTATAAAATAATGCCCTGAAA TA T FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1287058732 Functional Loss DEL TCGA 33..33 33 COAD,UCEC 2 - Human_RBP_ID_69843,Human_RBP_ID_598524 113433 RMVar_ID_113433 Human_SNP_ID_848937979 m1A Human chr3 + 52455676 52455676 52455676 GGCGACCGCGCGCACCTTCGGGCCCGAGCGGGAAGCCGAGCCGGCCAAGGAAGCGCGCGTCGTGG GGCGACCGCGCGCACCTTCGGGCCCGAGCGGGGAGCCGAGCCGGCCAAGGAAGCGCGCGTCGTGG A G NISCH Ensembl:ENSG00000010322 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:52455626..52455792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 4 oesophagus Human_RBP_ID_4757304,Human_RBP_ID_5206580,Human_RBP_ID_26763008 Human_Splice_Rec_438204,Human_Splice_Rec_438205,Human_Splice_Rec_438245,Human_Splice_Rec_438285,Human_Splice_Rec_438309 RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_218661 113434 RMVar_ID_113434 Human_SNP_ID_848962726 m1A Human chr3 + 141311614 141311614 141311614 AGTGCCCAAGCCTGTCTCTCACGTTCCACCCCATAAACCTTCCCCACCCGACCAGAAGCCAGAGA AGTGCCCAAGCCTGTCTCTCACGTTCCACCCCGTAAACCTTCCCCACCCGACCAGAAGCCAGAGA A G PXYLP1 Ensembl:ENSG00000155893 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:141311497..141311624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 113435 RMVar_ID_113435 Human_SNP_ID_849011003 m1A Human chr3 + 49022730 49022729 49022730 ACAGGTGGGATCCCACCAGGACATCACCGAAGACAGCTTTTCCCTCTTCTGGTTGCTGGAGCCCC ACAGGTGGGATCCCACCAGGACATCACCGAAG_CAGCTTTTCCCTCTTCTGGTTGCTGGAGCCCC GA G NDUFAF3 Ensembl:ENSG00000178057 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:49022701..49022775 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 MELA 1 - Human_RBP_ID_603962,Human_RBP_ID_1964466,Human_RBP_ID_4745828,Human_RBP_ID_9141409,Human_RBP_ID_18007173,Human_RBP_ID_27055006 Human_Splice_Rec_427078,Human_Splice_Rec_427079,Human_Splice_Rec_427086,Human_Splice_Rec_427087,Human_Splice_Rec_427094,Human_Splice_Rec_427095,Human_Splice_Rec_427100,Human_Splice_Rec_427101,Human_Splice_Rec_427108,Human_Splice_Rec_427112,Human_Splice_Rec_427113 Human_miRNA_ID_2405470,Human_miRNA_ID_2408465,Human_miRNA_ID_2411457,Human_miRNA_ID_2414436,Human_miRNA_ID_2622946 RMVar_hsa_circ_95686,RMVar_hsa_circ_218031 113436 RMVar_ID_113436 Human_SNP_ID_849012740 m1A Human chr3 - 100400853 100400853 100400853 GGGTGGGCGGCGGCGGGACTGCGGGCCCGGGCACGGGGGGGCTGCCGCGATGGCAGCTGGCTCTG GGGTGGGCGGCGGCGGGACTGCGGGCCCGGGCGCGGGGGGGCTGCCGCGATGGCAGCTGGCTCTG T C TOMM70 Ensembl:ENSG00000154174 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:100386952..100401068 26863196 MeRIP-seq:(Medium) rs546607944 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_247438,Human_RBP_ID_783534,Human_RBP_ID_836508,Human_RBP_ID_4714924,Human_RBP_ID_5241542,Human_RBP_ID_5325281,Human_RBP_ID_8875584,Human_RBP_ID_9302423,Human_RBP_ID_22456071,Human_RBP_ID_27041485 RMVar_hsa_circ_96874,RMVar_hsa_circ_220008,RMVar_hsa_circ_119266,RMVar_hsa_circ_220015 113437 RMVar_ID_113437 Human_SNP_ID_849032786 m1A Human chr3 - 48187922 48187922 48187922 CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCACCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC CGCCGCCATGGAACTGGGCCCGGAGCCCCCGCCCCGCCGCCGCCTGCTCTTCGCCTGCAGCCCCC T G CDC25A Ensembl:ENSG00000164045 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:48187826..48188290 26863410 MeRIP-seq:(Medium) rs994319712 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_22456582 113438 RMVar_ID_113438 Human_SNP_ID_849042886 m1A Human chr3 - 184321328 184321328 184321328 GGCTGGGATTCTGAAGGGCTATGCTCTGGGCCAGGCAGCCCTGGCCGGTCAGCAATGATTGCTCC GGCTGGGATTCTGAAGGGCTATGCTCTGGGCCGGGCAGCCCTGGCCGGTCAGCAATGATTGCTCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Hypoxia IP chr3:184321301..184321375;chr3:184321276..184321375 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 13 kidney 113439 RMVar_ID_113439 Human_SNP_ID_849053450 m1A Human chr3 + 10142047 10142040 10142047 CGGGCGGCCGCGGCCCGTGCTGCGCTCGGTGAACTCGCGCGAGCCCTCCCAGGTCATCTTCTGCA CGGGCGGCCGCGGCCCGTGCTGCGCT_______CTCGCGCGAGCCCTCCCAGGTCATCTTCTGCA TCGGTGAA T VHL Ensembl:ENSG00000134086 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:10141800..10142097 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 27..33 33 RECA 1 - Human_RBP_ID_584597,Human_RBP_ID_1615076,Human_RBP_ID_9393296,Human_RBP_ID_14554137,Human_RBP_ID_18793174,Human_RBP_ID_23119954,Human_RBP_ID_27042012,Human_RBP_ID_27311217,Human_RBP_ID_27496404 113440 RMVar_ID_113440 Human_SNP_ID_849070826 m1A Human chr3 - 15304196 15304196 15304196 GCTCGTCAGAAGTTCCGCTCTGTTCTGGTTGAAGCAACGGTGAAACTGGATGAACTGGTGAAGAA GCTCGTCAGAAGTTCCGCTCTGTTCTGGTTGACGCAACGGTGAAACTGGATGAACTGGTGAAGAA T G SH3BP5 Ensembl:ENSG00000131370 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:15304063..15304272 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_18799977,Human_RBP_ID_26347798,Human_RBP_ID_27821975 Human_Splice_Rec_398542,Human_Splice_Rec_398543,Human_Splice_Rec_398564,Human_Splice_Rec_398565,Human_Splice_Rec_398585,Human_Splice_Rec_398609,Human_Splice_Rec_398622,Human_Splice_Rec_398623,Human_Splice_Rec_398630 Human_miRNA_ID_2069576,Human_miRNA_ID_2802475 RMVar_hsa_circ_216169,RMVar_hsa_circ_369940,RMVar_hsa_circ_315080 113441 RMVar_ID_113441 Human_SNP_ID_849082471 m1A Human chr3 + 74614465 74614462 74614465 TCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG TCGCCGCCGCCGCCGCCGCCGCCGCCGCCG___CCGCCGCCGCCGCAGTTAGTCCGGGCCCGGGG GCCA G lnc-FRG2C-6 RNACentral:URS0000EB03BE lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:74614407..74614485 26863196 MeRIP-seq:(Medium) rs746683819 Functional Loss DEL ICGC 31..33 33 PBCA 3 - 113442 RMVar_ID_113442 Human_SNP_ID_849088537 m1A Human chr3 - 125520053 125520052 125520054 GCGGTCGGCAAGGAAGCGGAGGGGGCCGGAGAAGAGAGCTCTGGGGTCGACACGGTGAGGAGAAG GCGGTCGGCAAGGAAGCGGAGGGGGCCGGAG__GAGAGCTCTGGGGTCGACACGGTGAGGAGAAG CTT C SNX4 Ensembl:ENSG00000114520 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:125504676..125520200 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 SKCM 1 - Human_Splice_Rec_476905,Human_Splice_Rec_476931,Human_Splice_Rec_476963 113443 RMVar_ID_113443 Human_SNP_ID_849103906 m1A Human chr3 + 56613666 56613666 56613666 CTGGAGGAAGAGCAAAGAAAGAAGGAAGAACAAGAAGAGGAGCTTCGCTTAGCACAGGAACGTGA CTGGAGGAAGAGCAAAGAAAGAAGGAAGAACACGAAGAGGAGCTTCGCTTAGCACAGGAACGTGA A C CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:56613616..56613711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 READ 1 - Human_RBP_ID_247921,Human_RBP_ID_935518,Human_RBP_ID_22284759,Human_RBP_ID_24547275,Human_RBP_ID_26348196 Human_Splice_Rec_443532,Human_Splice_Rec_443533,Human_Splice_Rec_443574,Human_Splice_Rec_443575,Human_Splice_Rec_443608,Human_Splice_Rec_443609,Human_Splice_Rec_443674,Human_Splice_Rec_443675,Human_Splice_Rec_443718,Human_Splice_Rec_443719,Human_Splice_Rec_443760,Human_Splice_Rec_443761,Human_Splice_Rec_443786,Human_Splice_Rec_443787 RMVar_hsa_circ_22368,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218996,RMVar_hsa_circ_363721,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_58600,RMVar_hsa_circ_353235,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_59971,RMVar_hsa_circ_367613 113444 RMVar_ID_113444 Human_SNP_ID_849124763 m1A Human chr3 - 134250833 134250831 134250834 GCGGGCAGCCCCCAACTCCGGACGATGCAGCGAGGAGGCGGCGGCGGCGGCGCGCTCCGGAGGTC GCGGGCAGCCCCCAACTCCGGACGATGCAGC___GAGGCGGCGGCGGCGGCGCGCTCCGGAGGTC CCTC C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:134250476..134250850 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 LMS 3 - 113445 RMVar_ID_113445 Human_SNP_ID_849128672 m1A Human chr3 + 41224614 41224600 41224615 CACTGGCAGCAACAGTCTTACCTGGACTCTGGAATCCATTCTGGTGCCACTACCACAGCTCCTTC CACTGGCAGCAACAGTCTT_______________TCCATTCTGGTGCCACTACCACAGCTCCTTC TACCTGGACTCTGGAA T CTNNB1 Ensembl:ENSG00000168036 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:41224526..41225477 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 20..34 33 LICA 1 - Human_RBP_ID_601612,Human_RBP_ID_1626641,Human_RBP_ID_1962431,Human_RBP_ID_2783970,Human_RBP_ID_3707228,Human_RBP_ID_3963799,Human_RBP_ID_4765048,Human_RBP_ID_8572121,Human_RBP_ID_8871938,Human_RBP_ID_9302184,Human_RBP_ID_14816017,Human_RBP_ID_17290126,Human_RBP_ID_17403488,Human_RBP_ID_17519898,Human_RBP_ID_18005397,Human_RBP_ID_18807868,Human_RBP_ID_22456545,Human_RBP_ID_22605582,Human_RBP_ID_22823354,Human_RBP_ID_24001499,Human_RBP_ID_27052406,Human_RBP_ID_27317924 Human_Splice_Rec_414422,Human_Splice_Rec_414454,Human_Splice_Rec_414460,Human_Splice_Rec_414492,Human_Splice_Rec_414522,Human_Splice_Rec_414554,Human_Splice_Rec_414584,Human_Splice_Rec_414614,Human_Splice_Rec_414642,Human_Splice_Rec_414674,Human_Splice_Rec_414702,Human_Splice_Rec_414734,Human_Splice_Rec_414766,Human_Splice_Rec_414794,Human_Splice_Rec_414824,Human_Splice_Rec_414854,Human_Splice_Rec_414884,Human_Splice_Rec_414916,Human_Splice_Rec_414946,Human_Splice_Rec_414972,Human_Splice_Rec_415000,Human_Splice_Rec_415030,Human_Splice_Rec_415060,Human_Splice_Rec_415090,Human_Splice_Rec_415114,Human_Splice_Rec_415120,Human_Splice_Rec_415144,Human_Splice_Rec_415172,Human_Splice_Rec_415204,Human_Splice_Rec_415234,Human_Splice_Rec_415264,Human_Splice_Rec_415294,Human_Splice_Rec_415322,Human_Splice_Rec_415342,Human_Splice_Rec_415372,Human_Splice_Rec_415404,Human_Splice_Rec_415434,Human_Splice_Rec_415464,Human_Splice_Rec_415494,Human_Splice_Rec_415524,Human_Splice_Rec_415552,Human_Splice_Rec_415578,Human_Splice_Rec_415606,Human_Splice_Rec_415636,Human_Splice_Rec_415666,Human_Splice_Rec_415694 Human_miRNA_ID_2824079,Human_miRNA_ID_2824080,Human_miRNA_ID_2858051,Human_miRNA_ID_2858052 RMVar_hsa_circ_6296,RMVar_hsa_circ_295227,RMVar_hsa_circ_122575,RMVar_hsa_circ_265301,RMVar_hsa_circ_307807,RMVar_hsa_circ_347963,RMVar_hsa_circ_217163,RMVar_hsa_circ_371279,RMVar_hsa_circ_324096,RMVar_hsa_circ_304692,RMVar_hsa_circ_21583,RMVar_hsa_circ_282396,RMVar_hsa_circ_290509,RMVar_hsa_circ_274202,RMVar_hsa_circ_217165,RMVar_hsa_circ_217167,RMVar_hsa_circ_217168,RMVar_hsa_circ_217169,RMVar_hsa_circ_217166,RMVar_hsa_circ_85357,RMVar_hsa_circ_217164,RMVar_hsa_circ_113185,RMVar_hsa_circ_217170,RMVar_hsa_circ_217171,RMVar_hsa_circ_217172 113446 RMVar_ID_113446 Human_SNP_ID_849133195 m1A Human chr3 - 127573532 127573532 127573532 TCAACAGCACAGACAGCGAGCGCTGGAAGGCCATCAATGCCTGAGGGCAGCTGCCAGGGCCTGTG TCAACAGCACAGACAGCGAGCGCTGGAAGGCCGTCAATGCCTGAGGGCAGCTGCCAGGGCCTGTG T C TPRA1 Ensembl:ENSG00000163870 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:127573481..127573740 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_5149755,Human_RBP_ID_19012949 113447 RMVar_ID_113447 Human_SNP_ID_849140953 m1A Human chr3 + 52406884 52406884 52406884 CTCCATGATGACCCGCCGGGCCTTGTCTGTCCACTCCTCGTCCTCCCCCCAGGGCCCTAGTGGAG CTCCATGATGACCCGCCGGGCCTTGTCTGTCCGCTCCTCGTCCTCCCCCCAGGGCCCTAGTGGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52406810..52407455 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder 113448 RMVar_ID_113448 Human_SNP_ID_849156386 m1A Human chr3 + 185937928 185937928 185937928 ATCGAAGCTGCCAACCTCTTGCACCTTCCTTAAGGAGGCTCCGCCGCAGCCCCGCACGACGCGCC ATCGAAGCTGCCAACCTCTTGCACCTTCCTTATGGAGGCTCCGCCGCAGCCCCGCACGACGCGCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:185937826..185938025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 113449 RMVar_ID_113449 Human_SNP_ID_849168522 m1A Human chr3 + 119677269 119677269 119677269 GCGCAGCAGGGCTTCAGCGGCTTCTTCTCCTGAGACTCAGGCGGGGCAGGGTTTGAGTCAACCAG GCGCAGCAGGGCTTCAGCGGCTTCTTCTCCTGCGACTCAGGCGGGGCAGGGTTTGAGTCAACCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:119677164..119677405 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine tubulovillous,large_intestine adenocarcinoma,colon tubulovillous 6 large intestine 113450 RMVar_ID_113450 Human_SNP_ID_849182756 m1A Human chr3 - 48433807 48433807 48433807 TGTCCGAGAGGCTCGGGAGGACTTGGAAGTTCACCAGGCCAAGCTGAAGGAGGTGAGGGACCGCT TGTCCGAGAGGCTCGGGAGGACTTGGAAGTTCGCCAGGCCAAGCTGAAGGAGGTGAGGGACCGCT T C CCDC51 Ensembl:ENSG00000164051 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:48433146..48433940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_Splice_Rec_424282,Human_Splice_Rec_424288,Human_Splice_Rec_424294,Human_Splice_Rec_424306 RMVar_hsa_circ_123117,RMVar_hsa_circ_217850 113451 RMVar_ID_113451 Human_SNP_ID_849187869 m1A Human chr3 - 52402793 52402793 52402793 ATGAGGCGTGCCTCAAGGAGGAGGTAGAGAAGAGGAAGAAGTTCAAGGTGGGTGATTTCTCCAGT ATGAGGCGTGCCTCAAGGAGGAGGTAGAGAAGTGGAAGAAGTTCAAGGTGGGTGATTTCTCCAGT T A BAP1 Ensembl:ENSG00000163930 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:52402776..52402875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate Human_RBP_ID_605389,Human_RBP_ID_5602706,Human_RBP_ID_17704874,Human_RBP_ID_18013795,Human_RBP_ID_19010554,Human_RBP_ID_19115716 Human_Splice_Rec_437910,Human_Splice_Rec_437911,Human_Splice_Rec_437917,Human_Splice_Rec_437948,Human_Splice_Rec_437949,Human_Splice_Rec_437957,Human_Splice_Rec_437963 113452 RMVar_ID_113452 Human_SNP_ID_849208156 m1A Human chr3 + 128813597 128813583 128813597 AGTTACACCCCACATATCTCTCACACACACACACACACGCACACACACACACACAGATCTGACGT AGTTACACCCCACATATCT______________CACACGCACACACACACACACAGATCTGACGT TCTCACACACACACA T RAB7A Ensembl:ENSG00000075785 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:128813305..128813747 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 20..33 33 BRCA 1 - Human_RBP_ID_212713,Human_RBP_ID_2747450,Human_RBP_ID_9435453,Human_RBP_ID_17288153,Human_RBP_ID_17401562,Human_RBP_ID_17517016,Human_RBP_ID_24535454,Human_RBP_ID_26511710 Human_miRNA_ID_323796,Human_miRNA_ID_2205755 RMVar_hsa_circ_112866,RMVar_hsa_circ_221084,RMVar_hsa_circ_102059,RMVar_hsa_circ_97431,RMVar_hsa_circ_221090,RMVar_hsa_circ_114706,RMVar_hsa_circ_221091,RMVar_hsa_circ_87392,RMVar_hsa_circ_221096,RMVar_hsa_circ_123322,RMVar_hsa_circ_221097,RMVar_hsa_circ_221098 113453 RMVar_ID_113453 Human_SNP_ID_849209600 m1A Human chr3 - 129433946 129433946 129433946 GCCCCCCACGACGTAAAGCCTTTAAGAAATGGACACCTCCTCGGTCACCTTTTAATCTCGTTCAA GCCCCCCACGACGTAAAGCCTTTAAGAAATGGGCACCTCCTCGGTCACCTTTTAATCTCGTTCAA T C MBD4 Ensembl:ENSG00000129071 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:129433896..129434046 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_480862,Human_Splice_Rec_480863,Human_Splice_Rec_480876,Human_Splice_Rec_480877,Human_Splice_Rec_480888,Human_Splice_Rec_480889,Human_Splice_Rec_480902,Human_Splice_Rec_480903,Human_Splice_Rec_480922,Human_Splice_Rec_480923,Human_Splice_Rec_480929,Human_Splice_Rec_480938 RMVar_hsa_circ_366331,RMVar_hsa_circ_323484,RMVar_hsa_circ_62150,RMVar_hsa_circ_221157 113454 RMVar_ID_113454 Human_SNP_ID_849247429 m1A Human chr3 + 196470382 196470382 196470382 TTCAATGATCCAAACTGTCAGTCACCCCACCCAGCCTCATCTGGACCAGTTTCTGACGACCCAAT TTCAATGATCCAAACTGTCAGTCACCCCACCCGGCCTCATCTGGACCAGTTTCTGACGACCCAAT A G lnc-FBXO45-4 RNACentral:URS00008C0481 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:196470314..196470699 26863196 MeRIP-seq:(Medium) rs1232112453 Functional Loss SNV ICGC 33..33 33 LICA 1 - 113455 RMVar_ID_113455 Human_SNP_ID_849296894 m1A Human chr3 - 13375601 13375601 13375601 GGTCCACATACTACAGGTGCCTGTGTGGAACCAGCAGGAGGTGGAAATTCACATCCCGATCACCC GGTCCACATACTACAGGTGCCTGTGTGGAACCTGCAGGAGGTGGAAATTCACATCCCGATCACCC T A NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:13375551..13375650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_18013137 Human_Splice_Rec_396499,Human_Splice_Rec_396583 RMVar_hsa_circ_112106,RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_216041,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_117756,RMVar_hsa_circ_216046,RMVar_hsa_circ_109268,RMVar_hsa_circ_29455,RMVar_hsa_circ_216051,RMVar_hsa_circ_8821,RMVar_hsa_circ_216050,RMVar_hsa_circ_367268,RMVar_hsa_circ_377406,RMVar_hsa_circ_38044 113456 RMVar_ID_113456 Human_SNP_ID_849301964 m1A Human chr3 + 52231956 52231956 52231956 CCCACTGGCCCAGGACTCACGGGGGAGTTATCAGGCGACCAGGCGAGGAAGAGCCATTCGAAGCC CCCACTGGCCCAGGACTCACGGGGGAGTTATCTGGCGACCAGGCGAGGAAGAGCCATTCGAAGCC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:52231951..52232132 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113457 RMVar_ID_113457 Human_SNP_ID_849357839 m1A Human chr3 - 197749973 197749973 197749973 TGGCTCCCACCAACCGGGTACCAAACCGGTTCATGGCTGGAGACGTCGCGCCGAGAGCGGGCGCG TGGCTCCCACCAACCGGGTACCAAACCGGTTCGTGGCTGGAGACGTCGCGCCGAGAGCGGGCGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:197749923..197750012 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113458 RMVar_ID_113458 Human_SNP_ID_849381662 m1A Human chr3 - 128485874 128485874 128485874 CAGGCCTAGCTACTATGGGCACCCAGCCTGCTACACACCACCCCATCCCCACCTACCCCTCCTAT CAGGCCTAGCTACTATGGGCACCCAGCCTGCTGCACACCACCCCATCCCCACCTACCCCTCCTAT T C GATA2 Ensembl:ENSG00000179348 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:128485823..128485940 26863196 MeRIP-seq:(Medium) rs886057931 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach Human_RBP_ID_27497809 Clinvar_Rec_611 RMVar_hsa_circ_51147 113459 RMVar_ID_113459 Human_SNP_ID_849443523 m1A Human chr3 + 52706845 52706845 52706845 GTACGTGGCTGAACAGTTCGGGTGGACTGTCTATATAGTTATGGCCGGATTTGCTTTTTCATGTT GTACGTGGCTGAACAGTTCGGGTGGACTGTCTGTATAGTTATGGCCGGATTTGCTTTTTCATGTT A G SPCS1 Ensembl:ENSG00000114902 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52706776..52706914 32194978 MeRIP-seq:(Medium) rs778072787 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_605773,Human_RBP_ID_784396,Human_RBP_ID_934410,Human_RBP_ID_4757318,Human_RBP_ID_14894099,Human_RBP_ID_22456710,Human_RBP_ID_22768630,Human_RBP_ID_24011410,Human_RBP_ID_24498613 Human_Splice_Rec_439842,Human_Splice_Rec_439843,Human_Splice_Rec_439848,Human_Splice_Rec_439849,Human_Splice_Rec_439854,Human_Splice_Rec_439855,Human_Splice_Rec_439860,Human_Splice_Rec_439862,Human_Splice_Rec_439863 113460 RMVar_ID_113460 Human_SNP_ID_849459092 m1A Human chr3 + 51389048 51389048 51389048 ACTACATCCGGAAGATAAATGAACTGATGCCTAAATATGCCCCCAAGGCAGCCAGTGCACGGACC ACTACATCCGGAAGATAAATGAACTGATGCCTCAATATGCCCCCAAGGCAGCCAGTGCACGGACC A C MANF Ensembl:ENSG00000145050 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51387781..51389201 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 1 ovary Human_RBP_ID_604876,Human_RBP_ID_1313481,Human_RBP_ID_1629170,Human_RBP_ID_7207710,Human_RBP_ID_14881177,Human_RBP_ID_17661452,Human_RBP_ID_22455467,Human_RBP_ID_22768907,Human_RBP_ID_24498485,Human_RBP_ID_27320486 Human_miRNA_ID_337584,Human_miRNA_ID_795046 113461 RMVar_ID_113461 Human_SNP_ID_849480499 m1A Human chr3 - 124821426 124821426 124821426 GAAAGGATGCACTGCATTTGCTGGTGTTCACAACAGATGATGTGCCCCACATCGCATTGGATGGA GAAAGGATGCACTGCATTTGCTGGTGTTCACAGCAGATGATGTGCCCCACATCGCATTGGATGGA T C ITGB5 Ensembl:ENSG00000082781 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:124821376..124821475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_587814 Human_Splice_Rec_476374,Human_Splice_Rec_476432,Human_Splice_Rec_476440,Human_Splice_Rec_476456 Human_miRNA_ID_2296992 RMVar_hsa_circ_16955,RMVar_hsa_circ_58847,RMVar_hsa_circ_18849,RMVar_hsa_circ_364396,RMVar_hsa_circ_357955,RMVar_hsa_circ_365149,RMVar_hsa_circ_316427,RMVar_hsa_circ_220838,RMVar_hsa_circ_301315,RMVar_hsa_circ_357345,RMVar_hsa_circ_364220,RMVar_hsa_circ_345374,RMVar_hsa_circ_220840,RMVar_hsa_circ_278084,RMVar_hsa_circ_357204,RMVar_hsa_circ_363896,RMVar_hsa_circ_353290,RMVar_hsa_circ_67798,RMVar_hsa_circ_320347,RMVar_hsa_circ_220839,RMVar_hsa_circ_357724,RMVar_hsa_circ_275982,RMVar_hsa_circ_220841,RMVar_hsa_circ_107896,RMVar_hsa_circ_111685,RMVar_hsa_circ_220842 113462 RMVar_ID_113462 Human_SNP_ID_849491076 m1A Human chr3 + 186570839 186570839 186570839 GGCCTCACAGGGCCGGGTGGGCTGGCGAGCCGACGCGGCGGCGGAGGAGGCTGTGAGGAGTGTGT GGCCTCACAGGGCCGGGTGGGCTGGCGAGCCGGCGCGGCGGCGGAGGAGGCTGTGAGGAGTGTGT A G DNAJB11 Ensembl:ENSG00000090520 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:186570751..186570925 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUSC 1 - Human_RBP_ID_1311758,Human_RBP_ID_4734606,Human_RBP_ID_9394435,Human_RBP_ID_17661619,Human_RBP_ID_18471755,Human_RBP_ID_22456357,Human_RBP_ID_24547597,Human_RBP_ID_26347546 RMVar_hsa_circ_86211,RMVar_hsa_circ_223561 113463 RMVar_ID_113463 Human_SNP_ID_849496694 m1A Human chr3 + 49375588 49375588 49375588 CAACAATCACCAGTTTCTTCCGGATGGCAGCCATTGCTGAAACACAAAACACAGATATTACCTGC CAACAATCACCAGTTTCTTCCGGATGGCAGCCGTTGCTGAAACACAAAACACAGATATTACCTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr3:49375388..49375645;chr3:49375551..49375600;chr3:49375576..49375600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach 113464 RMVar_ID_113464 Human_SNP_ID_849502446 m1A Human chr3 + 154324311 154324311 154324311 ACCACCCCCTCCGCCGCCGCCGCCTCCTCCGGAGCCTCGGTTACCTCCATGACCCCCTGCTGGCC ACCACCCCCTCCGCCGCCGCCGCCTCCTCCGGGGCCTCGGTTACCTCCATGACCCCCTGCTGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:154324130..154324475;chr3:154324114..154324475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113465 RMVar_ID_113465 Human_SNP_ID_849512522 m1A Human chr3 - 48569762 48569762 48569762 GTTTGGGCGGGACTCACACTCTTTTGCCCAATAGGGTGATGTTGGGAGTGCAGGACTAAAGGGTG GTTTGGGCGGGACTCACACTCTTTTGCCCAATTGGGTGATGTTGGGAGTGCAGGACTAAAGGGTG T A COL7A1 Ensembl:ENSG00000114270 Protein coding intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr3:48569726..48569775;chr3:48569570..48569953 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_66968,Human_RBP_ID_2788438,Human_RBP_ID_24006709 Human_Splice_Rec_425037,Human_Splice_Rec_425269,Human_Splice_Rec_425313,Human_Splice_Rec_425335 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_124830,RMVar_hsa_circ_110617,RMVar_hsa_circ_217870,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_82639,RMVar_hsa_circ_217873,RMVar_hsa_circ_217871,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_217878,RMVar_hsa_circ_106133,RMVar_hsa_circ_82782,RMVar_hsa_circ_98848,RMVar_hsa_circ_217879,RMVar_hsa_circ_217880 113466 RMVar_ID_113466 Human_SNP_ID_849524469 m1A Human chr3 + 58433674 58433674 58433674 CCGGCGCGGTCCAGTGAAAGCGCCTCTTCAGCAGCCCGGAGACCTGGCAGGGAGAGAGGAAGATG CCGGCGCGGTCCAGTGAAAGCGCCTCTTCAGCGGCCCGGAGACCTGGCAGGGAGAGAGGAAGATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:58433608..58433708 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck 113467 RMVar_ID_113467 Human_SNP_ID_849528343 m1A Human chr3 + 141738401 141738401 141738401 ACCTGCGCCCTGGCCTCTCACTCCGGGAGCTCAGGCTCCAAGTCGGGAGGCGACAAGATGTTCTC ACCTGCGCCCTGGCCTCTCACTCCGGGAGCTCTGGCTCCAAGTCGGGAGGCGACAAGATGTTCTC A T RNF7 Ensembl:ENSG00000114125 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:141738350..141738446 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_1619013,Human_RBP_ID_4757485,Human_RBP_ID_17404718,Human_RBP_ID_22508846 113468 RMVar_ID_113468 Human_SNP_ID_849534837 m1A Human chr3 - 48583724 48583724 48583724 CAAGGCCCCGTTGGCCCCCCTGGAAAGAAAGGAGAAAAAGTAGGAAGGCTGACTTGATGATGTCC CAAGGCCCCGTTGGCCCCCCTGGAAAGAAAGGGGAAAAAGTAGGAAGGCTGACTTGATGATGTCC T C COL7A1 Ensembl:ENSG00000114270 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48583530..48583727 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_Splice_Rec_424916,Human_Splice_Rec_424917,Human_Splice_Rec_425146,Human_Splice_Rec_425147 RMVar_hsa_circ_102347,RMVar_hsa_circ_116636,RMVar_hsa_circ_110617,RMVar_hsa_circ_217872,RMVar_hsa_circ_217874,RMVar_hsa_circ_217873,RMVar_hsa_circ_82794,RMVar_hsa_circ_116423,RMVar_hsa_circ_217875,RMVar_hsa_circ_217877,RMVar_hsa_circ_86495,RMVar_hsa_circ_217876,RMVar_hsa_circ_98848,RMVar_hsa_circ_217880,RMVar_hsa_circ_78135,RMVar_hsa_circ_217881,RMVar_hsa_circ_114810,RMVar_hsa_circ_217883,RMVar_hsa_circ_109527,RMVar_hsa_circ_126151,RMVar_hsa_circ_117566,RMVar_hsa_circ_217887,RMVar_hsa_circ_217888,RMVar_hsa_circ_217889,RMVar_hsa_circ_121184,RMVar_hsa_circ_89357,RMVar_hsa_circ_217893,RMVar_hsa_circ_116920,RMVar_hsa_circ_217894,RMVar_hsa_circ_217895 113469 RMVar_ID_113469 Human_SNP_ID_849539984 m1A Human chr3 - 138103511 138103511 138103511 CCGCCGGCGTCGCAAGATGATCAGCACCCTGCAGCAGCTGCTAATGCAGACAGGCACCCACAGCT CCGCCGGCGTCGCAAGATGATCAGCACCCTGCTGCAGCTGCTAATGCAGACAGGCACCCACAGCT T A DZIP1L Ensembl:ENSG00000158163 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:138103469..138103553 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_Splice_Rec_488083,Human_Splice_Rec_488129,Human_Splice_Rec_488155 RMVar_hsa_circ_335302,RMVar_hsa_circ_102473,RMVar_hsa_circ_221628,RMVar_hsa_circ_61976 113470 RMVar_ID_113470 Human_SNP_ID_849567276 m1A Human chr3 - 196246205 196246205 196246205 CAGCCAAAGTGCTTCTAAAGCAATACGTGGGTAGGCCTGAAGAGGGGATATTTATTAAAACTATT CAGCCAAAGTGCTTCTAAAGCAATACGTGGGTGGGCCTGAAGAGGGGATATTTATTAAAACTATT T C PCYT1A Ensembl:ENSG00000161217 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:196246200..196246363 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_79342,RMVar_hsa_circ_112875,RMVar_hsa_circ_223886,RMVar_hsa_circ_223887,RMVar_hsa_circ_223888,RMVar_hsa_circ_122899,RMVar_hsa_circ_46685,RMVar_hsa_circ_223889,RMVar_hsa_circ_300119,RMVar_hsa_circ_223892 113471 RMVar_ID_113471 Human_SNP_ID_849567823 m1A Human chr3 + 52694048 52694048 52694048 CTATTTTTCTTTGTCACACAGGAAAACAGCTCAGGCATGTTTGCTGCAGAAGAGACAGGGGAGGC CTATTTTTCTTTGTCACACAGGAAAACAGCTCGGGCATGTTTGCTGCAGAAGAGACAGGGGAGGC A G GNL3 Ensembl:ENSG00000163938 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:52693541..52694244 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_605710,Human_RBP_ID_935457,Human_RBP_ID_1629750,Human_RBP_ID_4750012,Human_RBP_ID_5120577,Human_RBP_ID_5149737,Human_RBP_ID_5393280,Human_RBP_ID_7210362,Human_RBP_ID_9393764,Human_RBP_ID_18811913,Human_RBP_ID_19012581,Human_RBP_ID_22284379,Human_RBP_ID_22824698,Human_RBP_ID_23024076,Human_RBP_ID_24011364,Human_RBP_ID_25745804,Human_RBP_ID_26347003,Human_RBP_ID_27057238,Human_RBP_ID_27822328 Human_Splice_Rec_439586,Human_Splice_Rec_439587,Human_Splice_Rec_439634,Human_Splice_Rec_439635,Human_Splice_Rec_439660,Human_Splice_Rec_439661 Human_miRNA_ID_2881203 RMVar_hsa_circ_71418,RMVar_hsa_circ_218774,RMVar_hsa_circ_115939,RMVar_hsa_circ_310167,RMVar_hsa_circ_51460,RMVar_hsa_circ_218773,RMVar_hsa_circ_93588,RMVar_hsa_circ_218775 113472 RMVar_ID_113472 Human_SNP_ID_849579900 m1A Human chr3 + 194136248 194136248 194136248 CAGCGCTACTGATCACCAAGTAGCCACAAAATATAATAAACCCTCAGCACTTGCTCAGTAGTTTT CAGCGCTACTGATCACCAAGTAGCCACAAAATCTAATAAACCCTCAGCACTTGCTCAGTAGTTTT A C HES1 Ensembl:ENSG00000114315 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:194136147..194136375 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_308879,Human_RBP_ID_1624330,Human_RBP_ID_1958629,Human_RBP_ID_3701043,Human_RBP_ID_4757640,Human_RBP_ID_5425235,Human_RBP_ID_5447372,Human_RBP_ID_5474088,Human_RBP_ID_5506047,Human_RBP_ID_17402920,Human_RBP_ID_18002234,Human_RBP_ID_25723553,Human_RBP_ID_26824366 Human_miRNA_ID_2314825,Human_miRNA_ID_2317985,Human_miRNA_ID_2321143,Human_miRNA_ID_2324298,Human_miRNA_ID_2518679,Human_miRNA_ID_2521851,Human_miRNA_ID_2773685,Human_miRNA_ID_2821046,Human_miRNA_ID_2827179,Human_miRNA_ID_2830330,Human_miRNA_ID_2834448,Human_miRNA_ID_2839814,Human_miRNA_ID_2950206 RMVar_hsa_circ_100695,RMVar_hsa_circ_223709,RMVar_hsa_circ_96316,RMVar_hsa_circ_223710 113473 RMVar_ID_113473 Human_SNP_ID_849610725 m1A Human chr3 - 10125631 10125631 10125631 CTCGTTTAGTGTTGCAAGTCTTGAACGACAAGACATATCTGAGAAAAAGAGACTGGTGTTCAGGA CTCGTTTAGTGTTGCAAGTCTTGAACGACAAGGCATATCTGAGAAAAAGAGACTGGTGTTCAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:10125626..10125675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 113474 RMVar_ID_113474 Human_SNP_ID_849648711 m1A Human chr3 + 191329697 191329697 191329697 CTGGCCCGGTATGGCTGAAGTCAGCATCGACCAGTCCAAGCTGCCTGGAGTCAAGGAAGGTAAGG CTGGCCCGGTATGGCTGAAGTCAGCATCGACCTGTCCAAGCTGCCTGGAGTCAAGGAAGGTAAGG A T CCDC50 Ensembl:ENSG00000152492 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:191329601..191329725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_597317,Human_RBP_ID_934114,Human_RBP_ID_9394460,Human_RBP_ID_26346386 Human_Splice_Rec_523609,Human_Splice_Rec_523629 113475 RMVar_ID_113475 Human_SNP_ID_849658847 m1A Human chr3 - 138570321 138570321 138570321 ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTACAGGTACTGAGTTATGAATTCTTAGATGATGG ATAAAAGATCTTCAAAAGGAGCAGAAAACTTTGCAGGTACTGAGTTATGAATTCTTAGATGATGG T C CEP70 Ensembl:ENSG00000114107 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1673608 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_RBP_ID_19118557,Human_RBP_ID_23018264 Human_Splice_Rec_489037,Human_Splice_Rec_489097,Human_Splice_Rec_489131,Human_Splice_Rec_489169,Human_Splice_Rec_489197,Human_Splice_Rec_489215,Human_Splice_Rec_489233,Human_Splice_Rec_489247 GWAS_ID_14533,GWAS_ID_14534,GWAS_ID_14535,GWAS_ID_14536,GWAS_ID_14537,GWAS_ID_14538 RMVar_hsa_circ_68372,RMVar_hsa_circ_38778,RMVar_hsa_circ_221679,RMVar_hsa_circ_13379,RMVar_hsa_circ_317158,RMVar_hsa_circ_270865,RMVar_hsa_circ_96880,RMVar_hsa_circ_221680,RMVar_hsa_circ_291358,RMVar_hsa_circ_221678,RMVar_hsa_circ_30245,RMVar_hsa_circ_221687,RMVar_hsa_circ_366269,RMVar_hsa_circ_221686,RMVar_hsa_circ_367399,RMVar_hsa_circ_348897,RMVar_hsa_circ_221691,RMVar_hsa_circ_273859,RMVar_hsa_circ_288279,RMVar_hsa_circ_221692,RMVar_hsa_circ_221689,RMVar_hsa_circ_221690,RMVar_hsa_circ_221688 113476 RMVar_ID_113476 Human_SNP_ID_849659350 m1A Human chr3 - 187729392 187729388 187729392 TCTGGTTAGTCCACAGAGCCCCCAGAAATCTGACTGCCAGCCCAACTCGCCCACAGAGTCCTGCA TCTGGTTAGTCCACAGAGCCCCCAGAAATCTG____CCAGCCCAACTCGCCCACAGAGTCCTGCA GCAGT G BCL6 Ensembl:ENSG00000113916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:187729278..187729556 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..36 33 LGG 1 - Human_miRNA_ID_1013278,Human_miRNA_ID_1295279,Human_miRNA_ID_1299236 RMVar_hsa_circ_365430,RMVar_hsa_circ_57705 113477 RMVar_ID_113477 Human_SNP_ID_849661318 m1A Human chr3 - 4983502 4983502 4983502 CTGCGGCAGAGGCGTTGAGGCCTGGGTATAGCACTGGCACTGAGGTGGGATACCAGCACTTCTCC CTGCGGCAGAGGCGTTGAGGCCTGGGTATAGCGCTGGCACTGAGGTGGGATACCAGCACTTCTCC T C lnc-SUMF1-18 RNACentral:URS0000D5DE10 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:4983451..4983598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 113478 RMVar_ID_113478 Human_SNP_ID_849666520 m1A Human chr3 - 63838501 63838501 63838501 TATCTTTATTTTGGTTTTCTTTCTTTTTCATTAGATATAGCCAGTACCAACGTATGCTGAGCACG TATCTTTATTTTGGTTTTCTTTCTTTTTCATTTGATATAGCCAGTACCAACGTATGCTGAGCACG T A THOC7 Ensembl:ENSG00000163634 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:63838479..63839735 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 3 biliary tract,gallbladder Human_RBP_ID_7220060 RMVar_hsa_circ_5518,RMVar_hsa_circ_219385,RMVar_hsa_circ_90217,RMVar_hsa_circ_219387,RMVar_hsa_circ_328494,RMVar_hsa_circ_219388,RMVar_hsa_circ_22515,RMVar_hsa_circ_353782,RMVar_hsa_circ_219390 113479 RMVar_ID_113479 Human_SNP_ID_849666880 m1A Human chr3 + 52235081 52235081 52235081 ATGAGCCGCACAGAGCCAGCCCGTGCCTTGGCAAAGAATTCCTTCAGCTCTTCCGTGGCTATAAG ATGAGCCGCACAGAGCCAGCCCGTGCCTTGGCGAAGAATTCCTTCAGCTCTTCCGTGGCTATAAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52234984..52235158 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113480 RMVar_ID_113480 Human_SNP_ID_849667726 m1A Human chr3 - 57597199 57597199 57597199 TCGTTTAGTTTGCCTGGGAGCTTGAAAGGAGAAAGCACGGGGTCGCCCCAAACCCCTTCTGCTTC TCGTTTAGTTTGCCTGGGAGCTTGAAAGGAGATAGCACGGGGTCGCCCCAAACCCCTTCTGCTTC T A ARF4 Ensembl:ENSG00000168374 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr3:57597151..57597250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_68779,Human_RBP_ID_783890,Human_RBP_ID_936567,Human_RBP_ID_4758148,Human_RBP_ID_5530951,Human_RBP_ID_7214545,Human_RBP_ID_8577135,Human_RBP_ID_14909365,Human_RBP_ID_20930193,Human_RBP_ID_22398755,Human_RBP_ID_22824795,Human_RBP_ID_24013831,Human_RBP_ID_27058018 Human_Splice_Rec_445016,Human_Splice_Rec_445032 RMVar_hsa_circ_76920,RMVar_hsa_circ_219107,RMVar_hsa_circ_219108 113481 RMVar_ID_113481 Human_SNP_ID_849686869 m1A Human chr3 - 168043436 168043436 168043436 GGGAAGACTTCAGTAGAACATTTAATGACCATAAGCAAAAATACTTGCAGCTCCAGCAAGAAAAA GGGAAGACTTCAGTAGAACATTTAATGACCATTAGCAAAAATACTTGCAGCTCCAGCAAGAAAAA T A GOLIM4 Ensembl:ENSG00000173905 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr3:168043385..168043486 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_69057,Human_RBP_ID_282512,Human_RBP_ID_2762234,Human_RBP_ID_9348626,Human_RBP_ID_26348487 Human_Splice_Rec_504842,Human_Splice_Rec_504843,Human_Splice_Rec_504872,Human_Splice_Rec_504873,Human_Splice_Rec_504894,Human_Splice_Rec_504895 Human_miRNA_ID_184861 RMVar_hsa_circ_350185,RMVar_hsa_circ_222510,RMVar_hsa_circ_361955,RMVar_hsa_circ_350980,RMVar_hsa_circ_222513,RMVar_hsa_circ_274182,RMVar_hsa_circ_299930,RMVar_hsa_circ_222514,RMVar_hsa_circ_222515,RMVar_hsa_circ_111996,RMVar_hsa_circ_324488,RMVar_hsa_circ_355478 113482 RMVar_ID_113482 Human_SNP_ID_849689877 m1A Human chr3 - 195867662 195867662 195867662 GGTCAGCAGCACCCACTATTACTTGCTGCCCGAGCGACCATCCTACCTGGAGCGCTACCAGCGCT GGTCAGCAGCACCCACTATTACTTGCTGCCCGGGCGACCATCCTACCTGGAGCGCTACCAGCGCT T C TNK2 Ensembl:ENSG00000061938 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:195867546..195867700 26863196 MeRIP-seq:(Medium) rs778020093 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_4736130,Human_RBP_ID_26825201 RMVar_hsa_circ_20195,RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 113483 RMVar_ID_113483 Human_SNP_ID_849696030 m1A Human chr3 + 14112927 14112927 14112927 ATCCCTCCTCTTCTTTGGTTGCAGTGGCCTCAATGGGAGCTGTTTCTTCTGCTTGTTCTGCTGGC ATCCCTCCTCTTCTTTGGTTGCAGTGGCCTCAGTGGGAGCTGTTTCTTCTGCTTGTTCTGCTGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:14112914..14113029 26863196 MeRIP-seq:(Medium) rs751845757 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_lower_lobe adenocarcinoma,LUAD 4 lung 113484 RMVar_ID_113484 Human_SNP_ID_849708050 m1A Human chr3 - 46689427 46689427 46689427 CTGAGTCCGGCACCTGGCCATGTGCAACCCTGAGGAGGCAGCTCTGCTGCGGCTGGAGGAGGTCT CTGAGTCCGGCACCTGGCCATGTGCAACCCTGTGGAGGCAGCTCTGCTGCGGCTGGAGGAGGTCT T A ALS2CL Ensembl:ENSG00000178038 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:46689376..46689449 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_Splice_Rec_420540,Human_Splice_Rec_420541,Human_Splice_Rec_420606,Human_Splice_Rec_420607,Human_Splice_Rec_420656,Human_Splice_Rec_420657,Human_Splice_Rec_420726,Human_Splice_Rec_420727,Human_Splice_Rec_420768,Human_Splice_Rec_420769 RMVar_hsa_circ_57807,RMVar_hsa_circ_115528,RMVar_hsa_circ_217470 113485 RMVar_ID_113485 Human_SNP_ID_849713602 m1A Human chr3 + 113948818 113948818 113948818 GGTGACAGGTGCAAATCATGACACAGAAGGGCAGTATGAAGCCTGTGAAGAAAAAGAAAACCGAA GGTGACAGGTGCAAATCATGACACAGAAGGGCGGTATGAAGCCTGTGAAGAAAAAGAAAACCGAA A G ZDHHC23 Ensembl:ENSG00000184307 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:113948638..113948901;chr3:113948633..113948896 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_Splice_Rec_469224 RMVar_hsa_circ_104145,RMVar_hsa_circ_220363,RMVar_hsa_circ_100386,RMVar_hsa_circ_120874,RMVar_hsa_circ_220364,RMVar_hsa_circ_220365 113486 RMVar_ID_113486 Human_SNP_ID_849713609 m1A Human chr3 + 113948818 113948818 113948818 GGTGACAGGTGCAAATCATGACACAGAAGGGCAGTATGAAGCCTGTGAAGAAAAAGAAAACCGAA GGTGACAGGTGCAAATCATGACACAGAAGGGCTGTATGAAGCCTGTGAAGAAAAAGAAAACCGAA A T ZDHHC23 Ensembl:ENSG00000184307 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:113948638..113948901;chr3:113948633..113948896 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 7 prostate Human_Splice_Rec_469224 RMVar_hsa_circ_104145,RMVar_hsa_circ_220363,RMVar_hsa_circ_100386,RMVar_hsa_circ_120874,RMVar_hsa_circ_220364,RMVar_hsa_circ_220365 113487 RMVar_ID_113487 Human_SNP_ID_849751576 m1A Human chr3 - 185937963 185937963 185937963 TGCGGAGCATTTCGGCTCTGAGCGGCTGGGCGACCGGCGCGTCGTGCGGGGCTGCGGCGGAGCCT TGCGGAGCATTTCGGCTCTGAGCGGCTGGGCGGCCGGCGCGTCGTGCGGGGCTGCGGCGGAGCCT T C TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr3:185937730..185938082;chr3:185937757..185938058 26863196 MeRIP-seq:(Medium) rs1045451749 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_247351,Human_RBP_ID_783383,Human_RBP_ID_836167,Human_RBP_ID_938563,Human_RBP_ID_1623979,Human_RBP_ID_4734527,Human_RBP_ID_5325757,Human_RBP_ID_5425196,Human_RBP_ID_5474046,Human_RBP_ID_5505979,Human_RBP_ID_8870402,Human_RBP_ID_8943593,Human_RBP_ID_9333986,Human_RBP_ID_14752532,Human_RBP_ID_18424111,Human_RBP_ID_18804365,Human_RBP_ID_22092062,Human_RBP_ID_22278932,Human_RBP_ID_22457605,Human_RBP_ID_23026566,Human_RBP_ID_23135075,Human_RBP_ID_26346381 RMVar_hsa_circ_116021,RMVar_hsa_circ_223534 113488 RMVar_ID_113488 Human_SNP_ID_849753786 m1A Human chr3 - 42600745 42600745 42600745 TGGCTGGCCTCCAGCCTGAGCGGGTCCCCGTGAGCAGAAGAGAAAGCACTGCCACTGCAGCCAAA TGGCTGGCCTCCAGCCTGAGCGGGTCCCCGTGGGCAGAAGAGAAAGCACTGCCACTGCAGCCAAA T C SEC22C Ensembl:ENSG00000093183 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:42600696..42600786 26863196 MeRIP-seq:(Medium) rs1320652299 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113489 RMVar_ID_113489 Human_SNP_ID_849781324 m1A Human chr3 - 184171596 184171596 184171596 TCGGAGGCTGGGCCTCCCCTCGCTGGGGGCTCACAGAAAGTCAAACAGCCCGAAATTCTTGGCTG TCGGAGGCTGGGCCTCCCCTCGCTGGGGGCTCTCAGAAAGTCAAACAGCCCGAAATTCTTGGCTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr3:184171520..184171665 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113490 RMVar_ID_113490 Human_SNP_ID_849815013 m1A Human chr3 - 49531675 49531675 49531675 CCAGGAACTGTGGTGCCAGCTTCTGACACCCGAGTAGGCTGGATGGGGCCTAGGGTTGGGGTTTG CCAGGAACTGTGGTGCCAGCTTCTGACACCCGGGTAGGCTGGATGGGGCCTAGGGTTGGGGTTTG T C BSN-DT RNACentral:URS00008C22A1 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49531626..49531675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 BLCA,UCEC,endometrium endometrioid_carcinoma 9 uterus 113491 RMVar_ID_113491 Human_SNP_ID_849816556 m1A Human chr3 - 113019602 113019602 113019602 TGCCGCCGGGCCTGGAGCCGTGGAACCGTGTGAGAATCCCTAAGGCGGGGAACCGCAGCGCAGTG TGCCGCCGGGCCTGGAGCCGTGGAACCGTGTGGGAATCCCTAAGGCGGGGAACCGCAGCGCAGTG T C NEPRO Ensembl:ENSG00000163608 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:113019505..113061807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_4716902,Human_RBP_ID_8555096,Human_RBP_ID_14566143,Human_RBP_ID_18424033,Human_RBP_ID_23959429 Human_Splice_Rec_467805,Human_Splice_Rec_467821,Human_Splice_Rec_467833,Human_Splice_Rec_467847,Human_Splice_Rec_467861,Human_Splice_Rec_467869,Human_Splice_Rec_467873,Human_Splice_Rec_467887,Human_Splice_Rec_467901,Human_Splice_Rec_467911,Human_Splice_Rec_467925,Human_Splice_Rec_467947,Human_Splice_Rec_467955,Human_Splice_Rec_467963,Human_Splice_Rec_467967,Human_Splice_Rec_467971,Human_Splice_Rec_467979,Human_Splice_Rec_467985,Human_Splice_Rec_467991 113492 RMVar_ID_113492 Human_SNP_ID_849831179 m1A Human chr3 - 71320405 71320405 71320405 ATCTGTGCAGCGGCTTAGAGACAAGACTGTACAGGGTGTGTATGTGAGTGTCTGTCCGTGGTAGA ATCTGTGCAGCGGCTTAGAGACAAGACTGTACCGGGTGTGTATGTGAGTGTCTGTCCGTGGTAGA T G AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:71320399..71320513 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_82550,RMVar_hsa_circ_219594,RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_316285,RMVar_hsa_circ_54457,RMVar_hsa_circ_64045,RMVar_hsa_circ_219617,RMVar_hsa_circ_304923,RMVar_hsa_circ_333764,RMVar_hsa_circ_286827,RMVar_hsa_circ_315358,RMVar_hsa_circ_219615,RMVar_hsa_circ_277768,RMVar_hsa_circ_343399,RMVar_hsa_circ_116417,RMVar_hsa_circ_219618 113493 RMVar_ID_113493 Human_SNP_ID_849856322 m1A Human chr3 + 184142355 184142355 184142355 CGAGTTCAGTGATGATTCTGGGGCTGACCAAGAAAAGGACAAAGTGAAGATGAAAGGTGTGAGAC CGAGTTCAGTGATGATTCTGGGGCTGACCAAGGAAAGGACAAAGTGAAGATGAAAGGTGTGAGAC A G EIF2B5 Ensembl:ENSG00000145191 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:184142304..184142402 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_3964412,Human_RBP_ID_18803529,Human_RBP_ID_19013173,Human_RBP_ID_27822770 Human_Splice_Rec_514687,Human_Splice_Rec_514717,Human_Splice_Rec_514747,Human_Splice_Rec_514775,Human_Splice_Rec_514805,Human_Splice_Rec_514835,Human_Splice_Rec_514865,Human_Splice_Rec_514895,Human_Splice_Rec_514923,Human_Splice_Rec_514953,Human_Splice_Rec_514983,Human_Splice_Rec_515011,Human_Splice_Rec_515041,Human_Splice_Rec_515065,Human_Splice_Rec_515089,Human_Splice_Rec_515105,Human_Splice_Rec_515123,Human_Splice_Rec_515149,Human_Splice_Rec_515187,Human_Splice_Rec_515215,Human_Splice_Rec_515251,Human_Splice_Rec_515279,Human_Splice_Rec_515301,Human_Splice_Rec_515320,Human_Splice_Rec_515321,Human_Splice_Rec_515347,Human_Splice_Rec_515363 RMVar_hsa_circ_21273,RMVar_hsa_circ_223287,RMVar_hsa_circ_73420,RMVar_hsa_circ_375025,RMVar_hsa_circ_16711,RMVar_hsa_circ_56215,RMVar_hsa_circ_267510,RMVar_hsa_circ_117000,RMVar_hsa_circ_7189,RMVar_hsa_circ_223290 113494 RMVar_ID_113494 Human_SNP_ID_849860393 m1A Human chr3 - 53229131 53229131 53229131 TGCATATCCTTTCCCCCACACCCCAGGGGAAGACGGGCCCTCCCAGATGGCCCTAGAAGATCTGG TGCATATCCTTTCCCCCACACCCCAGGGGAAGTCGGGCCCTCCCAGATGGCCCTAGAAGATCTGG T A TKT Ensembl:ENSG00000163931 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr3:53229035..53229150;chr3:53229001..53229150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate Human_RBP_ID_247610,Human_RBP_ID_783761,Human_RBP_ID_937248,Human_RBP_ID_3965352,Human_RBP_ID_4750461,Human_RBP_ID_18194626,Human_RBP_ID_22455483 Human_Splice_Rec_441188,Human_Splice_Rec_441214,Human_Splice_Rec_441230,Human_Splice_Rec_441240,Human_Splice_Rec_441266,Human_Splice_Rec_441294,Human_Splice_Rec_441318,Human_Splice_Rec_441344,Human_Splice_Rec_441352 Human_miRNA_ID_2008461 RMVar_hsa_circ_12957,RMVar_hsa_circ_48712,RMVar_hsa_circ_218879,RMVar_hsa_circ_101380,RMVar_hsa_circ_294065,RMVar_hsa_circ_348857,RMVar_hsa_circ_62840,RMVar_hsa_circ_31013,RMVar_hsa_circ_24863,RMVar_hsa_circ_17364,RMVar_hsa_circ_218880,RMVar_hsa_circ_342760,RMVar_hsa_circ_218882,RMVar_hsa_circ_218883,RMVar_hsa_circ_305635,RMVar_hsa_circ_374561 113495 RMVar_ID_113495 Human_SNP_ID_849865358 m1A Human chr3 - 49132992 49132992 49132992 TCGGAGGGACCGCTGGACAGACCTGGGAACTGACAGAGGGCCTGGAGGGAAACAGGCCAAAGACC TCGGAGGGACCGCTGGACAGACCTGGGAACTGTCAGAGGGCCTGGAGGGAAACAGGCCAAAGACC T A LAMB2 Ensembl:ENSG00000172037 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49132801..49133050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast basal_(triple-negative)_carcinoma 3 breast Human_RBP_ID_247792,Human_RBP_ID_783962,Human_RBP_ID_835971,Human_RBP_ID_9393629 RMVar_hsa_circ_85105,RMVar_hsa_circ_218080 113496 RMVar_ID_113496 Human_SNP_ID_849905400 m1A Human chr3 - 186789199 186789199 186789199 CTGTAGTATTGTAGAAAGTCTCAATGTCACGAAGAATCCTCTTGTCTTCTTCAGTAACAAAGTTT CTGTAGTATTGTAGAAAGTCTCAATGTCACGAGGAATCCTCTTGTCTTCTTCAGTAACAAAGTTT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:186789126..186789400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 113497 RMVar_ID_113497 Human_SNP_ID_849926311 m1A Human chr3 + 185292304 185292303 185292304 TCCAGCCTGGGTGACAGAGCGAGACTCCGTCTAAAAAAAAAAAAAAAGTTGAATTAACAATAAGG TCCAGCCTGGGTGACAGAGCGAGACTCCGTCT_AAAAAAAAAAAAAAGTTGAATTAACAATAAGG TA T MAP3K13 Ensembl:ENSG00000073803 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_79846,RMVar_hsa_circ_78256,RMVar_hsa_circ_223452,RMVar_hsa_circ_223453 113498 RMVar_ID_113498 Human_SNP_ID_849946438 m1A Human chr3 + 48274544 48274544 48274544 CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCACCAGGTCGCTTTTGCTGGGCTAGTAACATCAA CCCTCCCCGGAAAAACTCCAAGCTCCTAATTCGCCAGGTCGCTTTTGCTGGGCTAGTAACATCAA A G ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6442112 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_18006898 GWAS_ID_10674,GWAS_ID_10675,GWAS_ID_10676,GWAS_ID_10677,GWAS_ID_10678,GWAS_ID_10679,GWAS_ID_10680,GWAS_ID_10681 113499 RMVar_ID_113499 Human_SNP_ID_849960306 m1A Human chr3 - 48599685 48599678 48599685 CCTGCAGGAGGTGGATGCCAGTGTGGTACGTGAGATCTGCTCCAAGTACATCTATGACCAGTGCC CCTGCAGGAGGTGGATGCCAGTGTGGTACGTG_______CTCCAAGTACATCTATGACCAGTGCC GCAGATCT G UQCRC1 Ensembl:ENSG00000010256 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:48599605..48599709 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..39 33 KIRP 1 - Human_RBP_ID_603532,Human_RBP_ID_1033520,Human_RBP_ID_1633602,Human_RBP_ID_1964162,Human_RBP_ID_3963968,Human_RBP_ID_5149930,Human_RBP_ID_8872830,Human_RBP_ID_17660706,Human_RBP_ID_18471788,Human_RBP_ID_19010219,Human_RBP_ID_19115415,Human_RBP_ID_22455416 Human_Splice_Rec_425370,Human_Splice_Rec_425371,Human_Splice_Rec_425394,Human_Splice_Rec_425395,Human_Splice_Rec_425402,Human_Splice_Rec_425422,Human_Splice_Rec_425423 Human_miRNA_ID_2614580 RMVar_hsa_circ_3555,RMVar_hsa_circ_80381,RMVar_hsa_circ_112656,RMVar_hsa_circ_122632,RMVar_hsa_circ_121280,RMVar_hsa_circ_122197,RMVar_hsa_circ_116876,RMVar_hsa_circ_102894,RMVar_hsa_circ_111089,RMVar_hsa_circ_100636,RMVar_hsa_circ_217925,RMVar_hsa_circ_217929,RMVar_hsa_circ_79147,RMVar_hsa_circ_217931,RMVar_hsa_circ_75853,RMVar_hsa_circ_217932,RMVar_hsa_circ_217930,RMVar_hsa_circ_217927,RMVar_hsa_circ_217928,RMVar_hsa_circ_217926,RMVar_hsa_circ_217923,RMVar_hsa_circ_217924,RMVar_hsa_circ_217922 113500 RMVar_ID_113500 Human_SNP_ID_849972469 m1A Human chr3 + 49014004 49014004 49014004 GCTTCAGCATCATGGTTACTCCGGACCCCAGCACCCCAAGCCGCCTCGCCTGCCATGTCATGCAC GCTTCAGCATCATGGTTACTCCGGACCCCAGCCCCCCAAGCCGCCTCGCCTGCCATGTCATGCAC A C WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49013954..49014204 26863196 MeRIP-seq:(Medium) rs914842097 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_247910,Human_RBP_ID_836700,Human_RBP_ID_1628324,Human_RBP_ID_3710121,Human_RBP_ID_7204192,Human_RBP_ID_8574647,Human_RBP_ID_8872978,Human_RBP_ID_9302906,Human_RBP_ID_9435350,Human_RBP_ID_14863266,Human_RBP_ID_18810193,Human_RBP_ID_22090039,Human_RBP_ID_22282441,Human_RBP_ID_22824036,Human_RBP_ID_23023509,Human_RBP_ID_23115936,Human_RBP_ID_26823839,Human_RBP_ID_27054945,Human_RBP_ID_27319577,Human_RBP_ID_27502710 Human_miRNA_ID_1359746,Human_miRNA_ID_2683356 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 113501 RMVar_ID_113501 Human_SNP_ID_850016948 m1A Human chr3 + 143055106 143055105 143055106 CATCTCACAAAGATTCTCCTAGAGATGTTAGCAAAAAAGCCAAAAGGTAAATGCAAGTCATTTTT CATCTCACAAAGATTCTCCTAGAGATGTTAGC_AAAAAGCCAAAAGGTAAATGCAAGTCATTTTT CA C U2SURP Ensembl:ENSG00000163714 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_1951621,Human_RBP_ID_24547314,Human_RBP_ID_26347280,Human_RBP_ID_27823562 Human_Splice_Rec_493071,Human_Splice_Rec_493133,Human_Splice_Rec_493209,Human_Splice_Rec_493263 Human_miRNA_ID_185136,Human_miRNA_ID_2004400 RMVar_hsa_circ_81353,RMVar_hsa_circ_116960,RMVar_hsa_circ_108737,RMVar_hsa_circ_222036,RMVar_hsa_circ_222039,RMVar_hsa_circ_24022,RMVar_hsa_circ_222040,RMVar_hsa_circ_222042,RMVar_hsa_circ_95932,RMVar_hsa_circ_305563,RMVar_hsa_circ_222041 113502 RMVar_ID_113502 Human_SNP_ID_850028449 m1A Human chr3 - 119498652 119498652 119498652 CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTACGAGGTGAGAATCCGTGCATTTGACCCAGGTT CTCGCGGACGTGCCGCGGGAGAGCGTAACTGTGCGAGGTGAGAATCCGTGCATTTGACCCAGGTT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr3:119498570..119498663 26863410 MeRIP-seq:(Medium) rs994397031 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck 113503 RMVar_ID_113503 Human_SNP_ID_850054067 m1A Human chr3 + 15635577 15635577 15635577 GAATATTATGTGGCTGCCGTGTATGAGCATCCATCCATCCTGAGTCTGAACCCTCTGGCTCTCAT GAATATTATGTGGCTGCCGTGTATGAGCATCCGTCCATCCTGAGTCTGAACCCTCTGGCTCTCAT A G BTD Ensembl:ENSG00000169814 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:15635528..15635628 32194978 MeRIP-seq:(Medium) rs1159185297 Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - RMVar_hsa_circ_87295,RMVar_hsa_circ_216208,RMVar_hsa_circ_343916,RMVar_hsa_circ_68742 113504 RMVar_ID_113504 Human_SNP_ID_850071806 m1A Human chr3 - 52679702 52679702 52679702 TCTTATAGAAGAAGTTGGATTCCATGGGTTCCAAGAGAAGAAGAGCTACCTCCCCTTCCAGCAGT TCTTATAGAAGAAGTTGGATTCCATGGGTTCCCAGAGAAGAAGAGCTACCTCCCCTTCCAGCAGT T G PBRM1 Ensembl:ENSG00000163939 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr3:52679651..52679785;chr3:52679651..52679797 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_935453,Human_RBP_ID_1965736,Human_RBP_ID_3964127,Human_RBP_ID_5206591,Human_RBP_ID_8236047,Human_RBP_ID_8576206,Human_RBP_ID_9393756,Human_RBP_ID_18008367,Human_RBP_ID_18424236,Human_RBP_ID_18811834,Human_RBP_ID_19010595 Human_Splice_Rec_438938,Human_Splice_Rec_439486,Human_Splice_Rec_439500,Human_Splice_Rec_439508,Human_Splice_Rec_439516,Human_Splice_Rec_439526,Human_Splice_Rec_439532,Human_Splice_Rec_439540 Human_miRNA_ID_1913549,Human_miRNA_ID_1915998,Human_miRNA_ID_1918447,Human_miRNA_ID_1920903,Human_miRNA_ID_1923360,Human_miRNA_ID_1925811,Human_miRNA_ID_1928261,Human_miRNA_ID_1930713,Human_miRNA_ID_3116300,Human_miRNA_ID_3124395 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_352306,RMVar_hsa_circ_45061,RMVar_hsa_circ_14249,RMVar_hsa_circ_48261,RMVar_hsa_circ_111221,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_299690,RMVar_hsa_circ_218723,RMVar_hsa_circ_360476,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_309126,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_35685,RMVar_hsa_circ_33167,RMVar_hsa_circ_218764,RMVar_hsa_circ_218752,RMVar_hsa_circ_120215,RMVar_hsa_circ_332668,RMVar_hsa_circ_349510,RMVar_hsa_circ_318672,RMVar_hsa_circ_218750,RMVar_hsa_circ_218751,RMVar_hsa_circ_293106,RMVar_hsa_circ_298720,RMVar_hsa_circ_218753,RMVar_hsa_circ_218759,RMVar_hsa_circ_301757,RMVar_hsa_circ_317816,RMVar_hsa_circ_338034,RMVar_hsa_circ_309271,RMVar_hsa_circ_218760,RMVar_hsa_circ_218757,RMVar_hsa_circ_218758,RMVar_hsa_circ_46295,RMVar_hsa_circ_314612,RMVar_hsa_circ_325776,RMVar_hsa_circ_360628,RMVar_hsa_circ_218762,RMVar_hsa_circ_218763,RMVar_hsa_circ_293695,RMVar_hsa_circ_218761,RMVar_hsa_circ_279744,RMVar_hsa_circ_66719,RMVar_hsa_circ_282016,RMVar_hsa_circ_291508,RMVar_hsa_circ_309743,RMVar_hsa_circ_276964,RMVar_hsa_circ_218765,RMVar_hsa_circ_218767,RMVar_hsa_circ_218768,RMVar_hsa_circ_218766,RMVar_hsa_circ_12920 113505 RMVar_ID_113505 Human_SNP_ID_850073615 m1A Human chr3 + 42581820 42581820 42581820 AACCCGCCTGCTCTTGGCTAACGGGCCGCGGCACCCGCCTCCGCCCGCCAGCCCTCACCTCGCCC AACCCGCCTGCTCTTGGCTAACGGGCCGCGGCCCCCGCCTCCGCCCGCCAGCCCTCACCTCGCCC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:42581810..42581950 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_217239 113506 RMVar_ID_113506 Human_SNP_ID_850078746 m1A Human chr3 + 127618062 127618062 127618062 CTCACGCTTTGACATCCTGTGTGTGGTGAGGGACACCGTGGACCCAGTCCAGGTATAGCTCACAT CTCACGCTTTGACATCCTGTGTGTGGTGAGGGTCACCGTGGACCCAGTCCAGGTATAGCTCACAT A T MCM2 Ensembl:ENSG00000073111 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:127617935..127618125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_938531,Human_RBP_ID_1617029,Human_RBP_ID_1948537,Human_RBP_ID_3685123,Human_RBP_ID_8557703,Human_RBP_ID_8867658,Human_RBP_ID_9394043,Human_RBP_ID_19116072,Human_RBP_ID_22455538,Human_RBP_ID_26824071 Human_Splice_Rec_479094,Human_Splice_Rec_479095,Human_Splice_Rec_479124,Human_Splice_Rec_479125,Human_Splice_Rec_479188,Human_Splice_Rec_479189,Human_Splice_Rec_479199 Human_miRNA_ID_1980165,Human_miRNA_ID_1981890,Human_miRNA_ID_2541320,Human_miRNA_ID_2545059,Human_miRNA_ID_2557924 RMVar_hsa_circ_38817,RMVar_hsa_circ_120433,RMVar_hsa_circ_97888,RMVar_hsa_circ_220995,RMVar_hsa_circ_220996,RMVar_hsa_circ_221000,RMVar_hsa_circ_76922,RMVar_hsa_circ_221001,RMVar_hsa_circ_78670 113507 RMVar_ID_113507 Human_SNP_ID_850098188 m1A Human chr3 + 187745338 187745338 187745338 GTAAAATAATGATCATGAGCAGCGGCGGCGGCAGCGGCACCAGCGGCAACAGCGGCGGCGGCGGC GTAAAATAATGATCATGAGCAGCGGCGGCGGCGGCGGCACCAGCGGCAACAGCGGCGGCGGCGGC A G AC072022.2 Ensembl:ENSG00000285938 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:187745327..187745428 26863196 MeRIP-seq:(Medium) rs1342857303 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_Splice_Rec_522554 113508 RMVar_ID_113508 Human_SNP_ID_850100144 m1A Human chr3 + 124773886 124773886 124773886 GTTGTCCCCGATGTAACCTGCATGGCACTTGCATTCCCCGCAGTGACACTCGCCATGGCCTAAAA GTTGTCCCCGATGTAACCTGCATGGCACTTGCCTTCCCCGCAGTGACACTCGCCATGGCCTAAAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:124773836..124773941 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 113509 RMVar_ID_113509 Human_SNP_ID_850123739 m1A Human chr3 - 49104473 49104473 49104473 CGCGGGGCTTCTCTCTTGACCCCTCTGACCTCAGGCTCAGCAGACCCTGGGTTCCACCATTGACA CGCGGGGCTTCTCTCTTGACCCCTCTGACCTCGGGCTCAGCAGACCCTGGGTTCCACCATTGACA T C QARS1 Ensembl:ENSG00000172053 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:49104282..49104516 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4757217 RMVar_hsa_circ_127195,RMVar_hsa_circ_218067,RMVar_hsa_circ_122582,RMVar_hsa_circ_218075 113510 RMVar_ID_113510 Human_SNP_ID_850136224 m1A Human chr3 - 196939324 196939324 196939324 CTGAAGAACAAATCTATGAACTCTTCAGCAAAAGTGGTGACATAAAGAAAATCATTATGGGTCTG CTGAAGAACAAATCTATGAACTCTTCAGCAAACGTGGTGACATAAAGAAAATCATTATGGGTCTG T G NCBP2 Ensembl:ENSG00000114503 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:196939273..196939423 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_598359,Human_RBP_ID_938953,Human_RBP_ID_1624808,Human_RBP_ID_1959310,Human_RBP_ID_3701962,Human_RBP_ID_8569016,Human_RBP_ID_9394515,Human_RBP_ID_14764641,Human_RBP_ID_18805332,Human_RBP_ID_22092131,Human_RBP_ID_22509336,Human_RBP_ID_22823019,Human_RBP_ID_23993372,Human_RBP_ID_26346387 Human_Splice_Rec_530853,Human_Splice_Rec_530859,Human_Splice_Rec_530867,Human_Splice_Rec_530879,Human_Splice_Rec_530885,Human_Splice_Rec_530889,Human_Splice_Rec_530897,Human_Splice_Rec_530903 Human_miRNA_ID_499101,Human_miRNA_ID_2171136 RMVar_hsa_circ_108700,RMVar_hsa_circ_223968 113511 RMVar_ID_113511 Human_SNP_ID_850148531 m1A Human chr3 - 10305577 10305577 10305577 CATCAAGAGGTTTGCATCAGGTGGCTGTGACAACCTCATCAAGCTGTGGAAGTAAGTAGGGATGT CATCAAGAGGTTTGCATCAGGTGGCTGTGACAGCCTCATCAAGCTGTGGAAGTAAGTAGGGATGT T C SEC13 Ensembl:ENSG00000157020 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:10305551..10305709 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm,liver hepatocellular_carcinoma 11 liver Human_RBP_ID_836918,Human_RBP_ID_932838,Human_RBP_ID_1030211,Human_RBP_ID_1945683,Human_RBP_ID_9128898,Human_RBP_ID_18194473,Human_RBP_ID_18445801,Human_RBP_ID_19115034,Human_RBP_ID_22455319,Human_RBP_ID_26824443,Human_RBP_ID_27496523 Human_Splice_Rec_393107,Human_Splice_Rec_393125,Human_Splice_Rec_393141,Human_Splice_Rec_393151,Human_Splice_Rec_393167,Human_Splice_Rec_393185,Human_Splice_Rec_393199,Human_Splice_Rec_393203 RMVar_hsa_circ_118440,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_278113,RMVar_hsa_circ_321863,RMVar_hsa_circ_127072,RMVar_hsa_circ_215835,RMVar_hsa_circ_215836 113512 RMVar_ID_113512 Human_SNP_ID_850161289 m1A Human chr3 + 134370970 134370970 134370970 ACAACTGAAGGAGCCGTTCACTCAACGAGCGCACGTGCCCATGCCTCAGCTCCCGCAGGGCCTCG ACAACTGAAGGAGCCGTTCACTCAACGAGCGCTCGTGCCCATGCCTCAGCTCCCGCAGGGCCTCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:134370921..134371114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 113513 RMVar_ID_113513 Human_SNP_ID_850169547 m1A Human chr3 + 136326890 136326890 136326890 TGCATTCAATATTCCACTCATCACTTTTGTTGATGTCCCTGGCTTTCTACCTGGTAAGTTTTTGA TGCATTCAATATTCCACTCATCACTTTTGTTGTTGTCCCTGGCTTTCTACCTGGTAAGTTTTTGA A T PCCB Ensembl:ENSG00000114054 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:136317050..136326928 32194978 MeRIP-seq:(Medium) rs1448763626 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_590216,Human_RBP_ID_22092512,Human_RBP_ID_22455586 Human_Splice_Rec_486980,Human_Splice_Rec_486981,Human_Splice_Rec_487004,Human_Splice_Rec_487005,Human_Splice_Rec_487030,Human_Splice_Rec_487031,Human_Splice_Rec_487058,Human_Splice_Rec_487059,Human_Splice_Rec_487084,Human_Splice_Rec_487085,Human_Splice_Rec_487114,Human_Splice_Rec_487115,Human_Splice_Rec_487142,Human_Splice_Rec_487143,Human_Splice_Rec_487160,Human_Splice_Rec_487161,Human_Splice_Rec_487188,Human_Splice_Rec_487189,Human_Splice_Rec_487220,Human_Splice_Rec_487221,Human_Splice_Rec_487266,Human_Splice_Rec_487267,Human_Splice_Rec_487316,Human_Splice_Rec_487340 RMVar_hsa_circ_25215,RMVar_hsa_circ_100419,RMVar_hsa_circ_77693,RMVar_hsa_circ_221539,RMVar_hsa_circ_221545,RMVar_hsa_circ_376375,RMVar_hsa_circ_221550,RMVar_hsa_circ_221549,RMVar_hsa_circ_116516,RMVar_hsa_circ_267536,RMVar_hsa_circ_221555,RMVar_hsa_circ_221557,RMVar_hsa_circ_273380,RMVar_hsa_circ_377426,RMVar_hsa_circ_271567,RMVar_hsa_circ_221556,RMVar_hsa_circ_221558,RMVar_hsa_circ_283798,RMVar_hsa_circ_298744,RMVar_hsa_circ_221559 113514 RMVar_ID_113514 Human_SNP_ID_850180503 m1A Human chr3 + 184180972 184180972 184180972 TCCTGGATGTGCTGGAGAGTGTGAACCTGCTCATGTCCCCACAAGGTGAGGTCCCTCTCACGACA TCCTGGATGTGCTGGAGAGTGTGAACCTGCTCGTGTCCCCACAAGGTGAGGTCCCTCTCACGACA A G AP2M1 Ensembl:ENSG00000161203 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr3:184180951..184180975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver Human_RBP_ID_936659,Human_RBP_ID_1623221,Human_RBP_ID_3965753,Human_RBP_ID_9303031,Human_RBP_ID_9333968,Human_RBP_ID_18013953,Human_RBP_ID_18803588,Human_RBP_ID_19013193,Human_RBP_ID_22457084,Human_RBP_ID_23115913,Human_RBP_ID_23989107,Human_RBP_ID_27841503 Human_Splice_Rec_515529,Human_Splice_Rec_515571,Human_Splice_Rec_515593,Human_Splice_Rec_515637,Human_Splice_Rec_515685,Human_Splice_Rec_515701,Human_Splice_Rec_515707,Human_Splice_Rec_515711 Human_miRNA_ID_2725031 RMVar_hsa_circ_103137,RMVar_hsa_circ_107035,RMVar_hsa_circ_123752,RMVar_hsa_circ_223302,RMVar_hsa_circ_223303,RMVar_hsa_circ_119742,RMVar_hsa_circ_20167,RMVar_hsa_circ_268836,RMVar_hsa_circ_223305,RMVar_hsa_circ_223306,RMVar_hsa_circ_113066,RMVar_hsa_circ_223308,RMVar_hsa_circ_79173,RMVar_hsa_circ_223310,RMVar_hsa_circ_223311 113515 RMVar_ID_113515 Human_SNP_ID_850260047 m1A Human chr3 + 51684469 51684469 51684469 GCCGTGGGCAGCATCCTGAGTGAAGGTGAGGAATCGCCCTCCCCTGAGCTCATCGACCTCTACCA GCCGTGGGCAGCATCCTGAGTGAAGGTGAGGATTCGCCCTCCCCTGAGCTCATCGACCTCTACCA A T TEX264 Ensembl:ENSG00000164081 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:51684405..51684506 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_4757276,Human_RBP_ID_22769274 Human_Splice_Rec_435092,Human_Splice_Rec_435094,Human_Splice_Rec_435110,Human_Splice_Rec_435120,Human_Splice_Rec_435128,Human_Splice_Rec_435138,Human_Splice_Rec_435144,Human_Splice_Rec_435148,Human_Splice_Rec_435156,Human_Splice_Rec_435164,Human_Splice_Rec_435176,Human_Splice_Rec_435182,Human_Splice_Rec_435188 Human_miRNA_ID_2893550,Human_miRNA_ID_2893551,Human_miRNA_ID_2997706,Human_miRNA_ID_2997707 RMVar_hsa_circ_78692,RMVar_hsa_circ_218544,RMVar_hsa_circ_121003,RMVar_hsa_circ_126568,RMVar_hsa_circ_289538,RMVar_hsa_circ_218545,RMVar_hsa_circ_218546,RMVar_hsa_circ_76938,RMVar_hsa_circ_218547,RMVar_hsa_circ_316075,RMVar_hsa_circ_218548,RMVar_hsa_circ_218549 113516 RMVar_ID_113516 Human_SNP_ID_850262603 m1A Human chr3 + 171460203 171460202 171460203 AGGCCCCGGGCCCAGCCTCCCCCGCCCACCCCAGCCCCACAGCGCCGGATCCCGATCCTCCGCGC AGGCCCCGGGCCCAGCCTCCCCCGCCCACCCC_GCCCCACAGCGCCGGATCCCGATCCTCCGCGC CA C AC092919.2 Ensembl:ENSG00000240497 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:171460155..171460408 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_Splice_Rec_506881 113517 RMVar_ID_113517 Human_SNP_ID_850286052 m1A Human chr3 + 49531826 49531826 49531826 GAGTATCCACACCAAAACCAGCAACGCCTTCAACTGACTCCACCACCACCACGACTCGCAGGCCA GAGTATCCACACCAAAACCAGCAACGCCTTCAGCTGACTCCACCACCACCACGACTCGCAGGCCA A G DAG1 Ensembl:ENSG00000173402 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr3:49531356..49532221;chr3:49531715..49531976;chr3:49531700..49531933 26863196 MeRIP-seq:(Medium) rs747370227 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_70267,Human_RBP_ID_1628593,Human_RBP_ID_17194907,Human_RBP_ID_17290505,Human_RBP_ID_17403808,Human_RBP_ID_18209901,Human_RBP_ID_27502979 113518 RMVar_ID_113518 Human_SNP_ID_850295560 m1A Human chr3 + 125864691 125864691 125864691 TCAGTGCCCCGATCCCTTATTTCTGTGCCCCAACCTCTTATCTCTGTGGCCCGATCCCTTATTTC TCAGTGCCCCGATCCCTTATTTCTGTGCCCCATCCTCTTATCTCTGTGGCCCGATCCCTTATTTC A T ENPP7P4 Ensembl:ENSG00000241278 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:125864623..125864909 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113519 RMVar_ID_113519 Human_SNP_ID_850298025 m1A Human chr3 + 49013488 49013488 49013488 ACCCTCGGTCACACGAGAAGCTGCACATCGTCAACTGTGGTGGAGGGCACCGTTCGTGGGCATTC ACCCTCGGTCACACGAGAAGCTGCACATCGTCCACTGTGGTGGAGGGCACCGTTCGTGGGCATTC A C WDR6 Ensembl:ENSG00000178252 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:49013438..49013523 26863196 MeRIP-seq:(Medium) rs751925913 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_1628296,Human_RBP_ID_1964437,Human_RBP_ID_2788974,Human_RBP_ID_3710116,Human_RBP_ID_8872964,Human_RBP_ID_14863238,Human_RBP_ID_18810177,Human_RBP_ID_23023506,Human_RBP_ID_27319571,Human_RBP_ID_27502697 Human_miRNA_ID_2054910 RMVar_hsa_circ_78740,RMVar_hsa_circ_88157,RMVar_hsa_circ_218022,RMVar_hsa_circ_218023 113520 RMVar_ID_113520 Human_SNP_ID_850326855 m1A Human chr3 - 185248516 185248516 185248516 GATTTACTTCATGTATTTTGTTTTCTTTTAGTACGACTTTACTCCGTGACATAAAAGAAGGACTA GATTTACTTCATGTATTTTGTTTTCTTTTAGTGCGACTTTACTCCGTGACATAAAAGAAGGACTA T C EHHADH Ensembl:ENSG00000113790 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:185248482..185248567 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_9395798 Human_Splice_Rec_519642,Human_Splice_Rec_519654,Human_Splice_Rec_519668,Human_Splice_Rec_519678,Human_Splice_Rec_519682 RMVar_hsa_circ_367413,RMVar_hsa_circ_295664,RMVar_hsa_circ_223449,RMVar_hsa_circ_351233,RMVar_hsa_circ_350000 113521 RMVar_ID_113521 Human_SNP_ID_850346106 m1A Human chr3 - 47413000 47413000 47413000 CTCTGGGGTCAAGGAGGCCAGCAATTCCAGGGAGGAGGAGGGGGGCCCCGAGCTGGGGGCTTCAG CTCTGGGGTCAAGGAGGCCAGCAATTCCAGGGGGGAGGAGGGGGGCCCCGAGCTGGGGGCTTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:47412950..47413220 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 113522 RMVar_ID_113522 Human_SNP_ID_850371421 m1A Human chr3 + 4303417 4303417 4303417 GGCAAAGACGACACGGCCTTGTGGGATGGCGGAGTTTAAGGAGAAGCCTGAGGCCCCGACTGAGC GGCAAAGACGACACGGCCTTGTGGGATGGCGGGGTTTAAGGAGAAGCCTGAGGCCCCGACTGAGC A G SETMAR Ensembl:ENSG00000170364 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr3:4303366..4303525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113523 RMVar_ID_113523 Human_SNP_ID_850394634 m1A Human chr3 + 52409605 52409605 52409605 GGTCGTAGATCTCCTCCACTTGCACCCCCTTGACACCTGCGATGAGGAAAGGAAAGCAGTAGGGA GGTCGTAGATCTCCTCCACTTGCACCCCCTTGTCACCTGCGATGAGGAAAGGAAAGCAGTAGGGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52409551..52409625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,kidney clear_cell_renal_cell_carcinoma,biliary_tract adenocarcinoma 4 kidney,biliary tract,gallbladder 113524 RMVar_ID_113524 Human_SNP_ID_850400032 m1A Human chr3 - 51391781 51391781 51391781 GTACTCAGGCGCGGCCGCGGATGAGCCGGGACACGCGGGCTCGGCCCCAGGCGGTGGCGGAGGCG GTACTCAGGCGCGGCCGCGGATGAGCCGGGACGCGCGGGCTCGGCCCCAGGCGGTGGCGGAGGCG T C lnc-DCAF1-1 RNACentral:URS0000D5C289 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr3:51391317..51391900 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113525 RMVar_ID_113525 Human_SNP_ID_850465561 m1A Human chr3 + 197951264 197951263 197951265 AAAATTGAAGGTGTTTACGCCCGAGATGAAACAGAATTCTATTTGGGCAAGAGATGCGCTTATGT AAAATTGAAGGTGTTTACGCCCGAGATGAAAC__AATTCTATTTGGGCAAGAGATGCGCTTATGT CAG C RPL35A Ensembl:ENSG00000182899 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:197950926..197951344 32194978 MeRIP-seq:(Medium) rs1560120302 Functional Loss DEL TCGA 33..34 33 UCEC 1 - Human_RBP_ID_598653,Human_RBP_ID_784193,Human_RBP_ID_1204939,Human_RBP_ID_1385478,Human_RBP_ID_1625040,Human_RBP_ID_1959760,Human_RBP_ID_4737603,Human_RBP_ID_8569394,Human_RBP_ID_9138461,Human_RBP_ID_14770123,Human_RBP_ID_17661313,Human_RBP_ID_18013679,Human_RBP_ID_18805626,Human_RBP_ID_21897832,Human_RBP_ID_22457199,Human_RBP_ID_22509358,Human_RBP_ID_23994129,Human_RBP_ID_27316813 Human_Splice_Rec_534625,Human_Splice_Rec_534631,Human_Splice_Rec_534639,Human_Splice_Rec_534647,Human_Splice_Rec_534661,Human_Splice_Rec_534669,Human_Splice_Rec_534677,Human_Splice_Rec_534681 Human_miRNA_ID_2349459 Clinvar_Rec_505 RMVar_hsa_circ_59217,RMVar_hsa_circ_75562,RMVar_hsa_circ_113145,RMVar_hsa_circ_224129,RMVar_hsa_circ_224130,RMVar_hsa_circ_124389,RMVar_hsa_circ_88697,RMVar_hsa_circ_224132,RMVar_hsa_circ_224133 113526 RMVar_ID_113526 Human_SNP_ID_850478237 m1A Human chr3 + 48695323 48695323 48695323 TCCTCCGGGCGCAGATGGCGGGGAGATGGGGGAGGCAGCGGAGTCCAGCGGCCAGTACGTCTTCT TCCTCCGGGCGCAGATGGCGGGGAGATGGGGGTGGCAGCGGAGTCCAGCGGCCAGTACGTCTTCT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48695273..48695423 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 12 large intestine 113527 RMVar_ID_113527 Human_SNP_ID_850505978 m1A Human chr3 + 195711037 195711037 195711037 CTGGTGAGTGAGTTAATTGAGATGAGGTGTGGAGGGACCTGGCTCCTGGTGAGTGAGTTAATTGA CTGGTGAGTGAGTTAATTGAGATGAGGTGTGGGGGGACCTGGCTCCTGGTGAGTGAGTTAATTGA A G SMBD1P,MUC20-OT1 Ensembl:ENSG00000283426,Ensembl:ENSG00000242086 Pseudogene,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:195710981..195711058 26863196 MeRIP-seq:(Medium) rs897959659 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_834331,Human_RBP_ID_9147242,Human_RBP_ID_17152367,Human_RBP_ID_18927132 RMVar_hsa_circ_66898 113528 RMVar_ID_113528 Human_SNP_ID_850535042 m1A Human chr3 + 52402839 52402839 52402839 TCCTTGAGGCACGCCTCATAGTTTGCAATCTCAGCCTCCACACACTTCAGCAGTGCCAGCAGCTC TCCTTGAGGCACGCCTCATAGTTTGCAATCTCGGCCTCCACACACTTCAGCAGTGCCAGCAGCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:52402771..52402889 26863196 MeRIP-seq:(Medium) rs753767419 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Clinvar_Rec_480 113529 RMVar_ID_113529 Human_SNP_ID_850558247 m1A Human chr3 + 48678580 48678580 48678580 AGCCACCTCCAGGCACCTTGTCTCCTGGTGACAGGTCTGCGATGTGCCGCACAGTGATGTCAATG AGCCACCTCCAGGCACCTTGTCTCCTGGTGACCGGTCTGCGATGTGCCGCACAGTGATGTCAATG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:48678576..48678625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach 113530 RMVar_ID_113530 Human_SNP_ID_850593510 m1A Human chr3 - 49101356 49101356 49101356 CAAAGCCATCAATTTCAACTTTGGCTATGCCAAGGTAAGCATGTGTCTAGGGACCTGGCAAGCAA CAAAGCCATCAATTTCAACTTTGGCTATGCCACGGTAAGCATGTGTCTAGGGACCTGGCAAGCAA T G QARS1 Ensembl:ENSG00000172053 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr3:49101351..49101450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_8574780,Human_RBP_ID_17291407,Human_RBP_ID_26823869 Human_Splice_Rec_427384,Human_Splice_Rec_427385,Human_Splice_Rec_427436,Human_Splice_Rec_427437,Human_Splice_Rec_427482,Human_Splice_Rec_427483,Human_Splice_Rec_427546,Human_Splice_Rec_427547,Human_Splice_Rec_427596,Human_Splice_Rec_427597,Human_Splice_Rec_427670,Human_Splice_Rec_427671,Human_Splice_Rec_427724,Human_Splice_Rec_427725,Human_Splice_Rec_427800,Human_Splice_Rec_427801,Human_Splice_Rec_427816,Human_Splice_Rec_427817,Human_Splice_Rec_427862,Human_Splice_Rec_427863,Human_Splice_Rec_427880,Human_Splice_Rec_427881,Human_Splice_Rec_427898,Human_Splice_Rec_427899,Human_Splice_Rec_427916,Human_Splice_Rec_427917,Human_Splice_Rec_427936,Human_Splice_Rec_427937,Human_Splice_Rec_427954 RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_218064,RMVar_hsa_circ_80230,RMVar_hsa_circ_80291,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_218065,RMVar_hsa_circ_25559,RMVar_hsa_circ_78406,RMVar_hsa_circ_218068 113531 RMVar_ID_113531 Human_SNP_ID_850627774 m1A Human chr3 + 52533601 52533601 52533601 TGGTGGGTGCCTGGGCGGGCGCGGAGCGCGGGACGCCGGGGCAGTGGGCGCCGGGACCCGGGGGG TGGTGGGTGCCTGGGCGGGCGCGGAGCGCGGGGCGCCGGGGCAGTGGGCGCCGGGACCCGGGGGG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr3:52533446..52533725;chr3:52533437..52534218 26863196 MeRIP-seq:(Medium) rs66782572 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,central_nervous_system oligodendroglioma_Grade_III,LICA,frontal_lobe oligodendroglioma_Grade_III 13 head and neck,brain GWAS_ID_10715,GWAS_ID_10716,GWAS_ID_10717,GWAS_ID_10718,GWAS_ID_10719,GWAS_ID_10720,GWAS_ID_10721,GWAS_ID_10722,GWAS_ID_10723,GWAS_ID_10724,GWAS_ID_10725,GWAS_ID_10726,GWAS_ID_10727,GWAS_ID_10728,GWAS_ID_10729,GWAS_ID_10730,GWAS_ID_10731,GWAS_ID_10732,GWAS_ID_10733,GWAS_ID_10734,GWAS_ID_10735,GWAS_ID_10736,GWAS_ID_10737,GWAS_ID_10738,GWAS_ID_10739,GWAS_ID_10740,GWAS_ID_10741,GWAS_ID_10742,GWAS_ID_10743,GWAS_ID_10744,GWAS_ID_10745,GWAS_ID_10746,GWAS_ID_10747,GWAS_ID_10748,GWAS_ID_10749,GWAS_ID_10750,GWAS_ID_10751,GWAS_ID_10752,GWAS_ID_10753,GWAS_ID_10754,GWAS_ID_10755,GWAS_ID_10756,GWAS_ID_10757 113532 RMVar_ID_113532 Human_SNP_ID_850629277 m1A Human chr3 + 129399359 129399356 129399360 CCTGGGAAGCAAAGTGAGACTCTGTCTCAAAAACAAACAAACAAACAAACTCACCGAGCAGGAAA CCTGGGAAGCAAAGTGAGACTCTGTCTCAA____AAACAAACAAACAAACTCACCGAGCAGGAAA AAAAC A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:129399226..129399405 26863196 MeRIP-seq:(Medium) rs568049924 Functional Loss DEL ICGC 31..34 33 PAAD 1 - 113533 RMVar_ID_113533 Human_SNP_ID_850632711 m1A Human chr3 - 65361160 65361160 65361160 CAAACTATGAAAACATTCCTTCCTTCCCTGGCATGACTCCATGAATTTGTCTCCAGAACGGCAGC CAAACTATGAAAACATTCCTTCCTTCCCTGGCGTGACTCCATGAATTTGTCTCCAGAACGGCAGC T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:65361157..65361300 26863196 MeRIP-seq:(Medium) rs1174175808 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - 113534 RMVar_ID_113534 Human_SNP_ID_850666185 m1A Human chr3 - 114859270 114859267 114859271 AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAGAATGGAAGGAAGGAGGAAAAGAAAGAAGAAAGGA AAAGAAGGAAGGAAGAAAGGAAGGAAGGAAG____GAAGGAAGGAGGAAAAGAAAGAAGAAAGGA CCATT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr3:114859220..114859299 26863196 MeRIP-seq:(Medium) rs138462352 Functional Loss DEL ICGC 32..35 33 NKTL 1 - RMVar_hsa_circ_86426,RMVar_hsa_circ_101902,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_20050,RMVar_hsa_circ_54355,RMVar_hsa_circ_21605,RMVar_hsa_circ_61207,RMVar_hsa_circ_55404,RMVar_hsa_circ_58848,RMVar_hsa_circ_366784,RMVar_hsa_circ_353408,RMVar_hsa_circ_220398 113535 RMVar_ID_113535 Human_SNP_ID_850679277 m1A Human chr3 - 195883311 195883311 195883311 AGTCCTGAGTCCTTGCAAATCCCGCTCTGGGCAGGTGAGTGTGGCTGTGAAGTGCCTGAAGCCCG AGTCCTGAGTCCTTGCAAATCCCGCTCTGGGCGGGTGAGTGTGGCTGTGAAGTGCCTGAAGCCCG T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr3:195883268..195883352 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_22677405 RMVar_hsa_circ_20195,RMVar_hsa_circ_280698,RMVar_hsa_circ_11259,RMVar_hsa_circ_310424,RMVar_hsa_circ_100106,RMVar_hsa_circ_223832,RMVar_hsa_circ_223831,RMVar_hsa_circ_94671,RMVar_hsa_circ_223833 113536 RMVar_ID_113536 Human_SNP_ID_850718636 m1A Human chr3 - 66500957 66500957 66500957 CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGAACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG CGGGACTCTTGCTGCGCGGAGGAGCCGTGCGGGACCCGAGGCTGCGCGCGCGCGCGCGCTCTCTG T C LRIG1 Ensembl:ENSG00000144749 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr3:66500852..66501021 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4756592,Human_RBP_ID_18424010 113537 RMVar_ID_113537 Human_SNP_ID_820848032 m1A Human chr14 - 90400070 90400070 90400070 AACTTACCAGCAATCTGTTCTTCGGTCAGCTGATCAGCCTATATGAAGAAAGAAAAGGTTATCAT AACTTACCAGCAATCTGTTCTTCGGTCAGCTGTTCAGCCTATATGAAGAAAGAAAAGGTTATCAT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:90400051..90400100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 5 breast 113538 RMVar_ID_113538 Human_SNP_ID_820855248 m1A Human chr14 - 105487258 105487258 105487258 CCTCCTTGTTGCACTTGGGACACTTGGGCATGACGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT CCTCCTTGTTGCACTTGGGACACTTGGGCATGGCGGCTCCGGGTCCGGTGCAGGCGGCAGCGGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105487161..105487438;chr14:105487201..105487372;chr14:105487201..105487360 26863196 MeRIP-seq:(Medium) rs7140395 Functional Loss SNV ICGC 33..33 33 COCA 5 - 113539 RMVar_ID_113539 Human_SNP_ID_820859556 m1A Human chr14 - 61547817 61547816 61547817 TTCAGCTGGGCCCAGTCGATTTCCTTAAAAAAAGGATGTCTCAAGATGGCGTGCTCGCCTCCCTG TTCAGCTGGGCCCAGTCGATTTCCTTAAAAAA_GGATGTCTCAAGATGGCGTGCTCGCCTCCCTG CT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:61530515..61547857 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 COAD,BRCA,UCEC 6 - 113540 RMVar_ID_113540 Human_SNP_ID_820871972 m1A Human chr14 + 67620024 67620024 67620024 CAGCCTCTCGCGTCTCCTCCAGACGCGAGTGCATTCCATCCTGAAGAAATCCGTCCACTCCGTGG CAGCCTCTCGCGTCTCCTCCAGACGCGAGTGCGTTCCATCCTGAAGAAATCCGTCCACTCCGTGG A G ARG2 Ensembl:ENSG00000081181 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17185189 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma,lung adenocarcinoma 3 lung Human_RBP_ID_9323798 Human_Splice_Rec_1528387,Human_Splice_Rec_1528401,Human_Splice_Rec_1528409 113541 RMVar_ID_113541 Human_SNP_ID_820874393 m1A Human chr14 - 21213001 21212989 21213002 AAACACTTCACGAAGGGGCAAAAGTGGCTTCAATTCTAAGAGTGGACAGCGGGGATCTTCCAAGT AAACACTTCACGAAGGGGCAAAAGTGGCTTC_____________GACAGCGGGGATCTTCCAAGT CCACTCTTAGAATT C HNRNPC Ensembl:ENSG00000092199 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:21212976..21213000 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 32..44 33 LUAD 2 - Human_RBP_ID_119825,Human_RBP_ID_443052,Human_RBP_ID_1490702,Human_RBP_ID_1816120,Human_RBP_ID_6330843,Human_RBP_ID_8401336,Human_RBP_ID_9039953,Human_RBP_ID_9368291,Human_RBP_ID_18647390,Human_RBP_ID_22797376,Human_RBP_ID_26922049,Human_RBP_ID_27225267 Human_Splice_Rec_1490675,Human_Splice_Rec_1490691,Human_Splice_Rec_1490705,Human_Splice_Rec_1490719,Human_Splice_Rec_1490731,Human_Splice_Rec_1490745,Human_Splice_Rec_1490761,Human_Splice_Rec_1490775,Human_Splice_Rec_1490791,Human_Splice_Rec_1490804,Human_Splice_Rec_1490805,Human_Splice_Rec_1490819,Human_Splice_Rec_1490849,Human_Splice_Rec_1490865,Human_Splice_Rec_1490881,Human_Splice_Rec_1490895,Human_Splice_Rec_1490915,Human_Splice_Rec_1490927,Human_Splice_Rec_1490943,Human_Splice_Rec_1490961,Human_Splice_Rec_1490965,Human_Splice_Rec_1490971 RMVar_hsa_circ_44974,RMVar_hsa_circ_165137,RMVar_hsa_circ_102923,RMVar_hsa_circ_292410,RMVar_hsa_circ_338118,RMVar_hsa_circ_110478,RMVar_hsa_circ_44097,RMVar_hsa_circ_51171,RMVar_hsa_circ_266464,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_372680,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730,RMVar_hsa_circ_165140 113542 RMVar_ID_113542 Human_SNP_ID_820887921 m1A Human chr14 + 104966263 104966263 104966263 CACCTTCCTACTGCTCCGGGGGCCAGGCCCAGACCCCTGGCCTCCATAACCCCCCAGCAGAGCCA CACCTTCCTACTGCTCCGGGGGCCAGGCCCAGCCCCCTGGCCTCCATAACCCCCCAGCAGAGCCA A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104966256..104966625 26863196 MeRIP-seq:(Medium) rs1057153172 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113543 RMVar_ID_113543 Human_SNP_ID_820894418 m1A Human chr14 + 102417686 102417686 102417686 TAGATGTTCAAGAAGCCAGAAGTGACTAGGGCACTGGCTATGGCTGGAGTCCAGGGGAGCCGTGG TAGATGTTCAAGAAGCCAGAAGTGACTAGGGCGCTGGCTATGGCTGGAGTCCAGGGGAGCCGTGG A G TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102417670..102417914 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_1036,RMVar_hsa_circ_45553,RMVar_hsa_circ_314981,RMVar_hsa_circ_288761,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_169406,RMVar_hsa_circ_317442,RMVar_hsa_circ_22690,RMVar_hsa_circ_169408,RMVar_hsa_circ_45590,RMVar_hsa_circ_127684,RMVar_hsa_circ_169409 113544 RMVar_ID_113544 Human_SNP_ID_820907484 m1A Human chr14 - 60972451 60972451 60972451 CCGCCGCCGCCGCCGCCATGCCCAAGAGAAAGACTGAAGGGGATGCTAAAGGAGATAAAGCCAAG CCGCCGCCGCCGCCGCCATGCCCAAGAGAAAGGCTGAAGGGGATGCTAAAGGAGATAAAGCCAAG T C TRMT5,AL160236.1 Ensembl:ENSG00000126814,Ensembl:ENSG00000258656 Protein coding,Pseudogene 3'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:60972299..60972559 26863196 MeRIP-seq:(Medium) rs1345095453 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,liver neoplasm,ESCA 3 liver,oesophagus 113545 RMVar_ID_113545 Human_SNP_ID_820914037 m1A Human chr14 + 104743172 104743172 104743172 GGCTCGACCTGATGATTCTAAGATATGCTCACATGGTCAACGGATTCACTGCGTAAGCAACCCAT GGCTCGACCTGATGATTCTAAGATATGCTCACGTGGTCAACGGATTCACTGCGTAAGCAACCCAT A G ADSS1 Ensembl:ENSG00000185100 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104743124..104743229 26863196 MeRIP-seq:(Medium) rs759674422 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_9370563 Human_Splice_Rec_1560497,Human_Splice_Rec_1560537,Human_Splice_Rec_1560561,Human_Splice_Rec_1560581,Human_Splice_Rec_1560591 RMVar_hsa_circ_74246,RMVar_hsa_circ_28385 113546 RMVar_ID_113546 Human_SNP_ID_820921796 m1A Human chr14 - 53041873 53041873 53041873 CCCCAACCTCCCCTCCACACATACACCTCTGTAATCTGATGCTTTAAGCTCAGATTAAAGCATCA CCCCAACCTCCCCTCCACACATACACCTCTGTTATCTGATGCTTTAAGCTCAGATTAAAGCATCA T A DDHD1 Ensembl:ENSG00000100523 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78389413 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_6356959 RMVar_hsa_circ_269123 113547 RMVar_ID_113547 Human_SNP_ID_820943881 m1A Human chr14 - 100687925 100687925 100687925 GATGACGGTGGCTGAGGGGTGGAGAGATGATGACGGTGGCTGAGGGATGGAGAGATGATGACGGT GATGACGGTGGCTGAGGGGTGGAGAGATGATGGCGGTGGCTGAGGGATGGAGAGATGATGACGGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100687846..100688147 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113548 RMVar_ID_113548 Human_SNP_ID_820957926 m1A Human chr14 + 49688157 49688157 49688157 AGCCCACTCACCCACGGAGCAGCAAGCCCCGCAACTTGAAGGCGGAGAGCGCCCGGCTCCGCAGC AGCCCACTCACCCACGGAGCAGCAAGCCCCGCGACTTGAAGGCGGAGAGCGCCCGGCTCCGCAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:49687989..49688156;chr14:49688032..49688157 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 113549 RMVar_ID_113549 Human_SNP_ID_820958473 m1A Human chr14 - 20993090 20993090 20993090 CGGATCTGAAGAAATATACAACATCCCACAGTAGGGTAATTAGATACTTATTTAGGACCTTGATA CGGATCTGAAGAAATATACAACATCCCACAGTGGGGTAATTAGATACTTATTTAGGACCTTGATA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:20993084..20993188 26863410 MeRIP-seq:(Medium) rs78713618 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA 4 stomach 113550 RMVar_ID_113550 Human_SNP_ID_820973484 m1A Human chr14 - 104775737 104775735 104775738 GGCTGACGGCCTCAAGAAGCAGGAGGAGGAGGAGATGGACTTCCGGTCGGGCTCACCCAGTGACA GGCTGACGGCCTCAAGAAGCAGGAGGAGGAG___ATGGACTTCCGGTCGGGCTCACCCAGTGACA TCTC T AKT1 Ensembl:ENSG00000142208 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104775686..104775845 26863196 MeRIP-seq:(Medium) rs768025881 Functional Loss DEL ICGC 32..34 33 CHOL 1 - Human_RBP_ID_3945163,Human_RBP_ID_18981124,Human_RBP_ID_22926374,Human_RBP_ID_26324786,Human_RBP_ID_26431901 Human_Splice_Rec_1560654,Human_Splice_Rec_1560655,Human_Splice_Rec_1560680,Human_Splice_Rec_1560681,Human_Splice_Rec_1560708,Human_Splice_Rec_1560709,Human_Splice_Rec_1560752,Human_Splice_Rec_1560753,Human_Splice_Rec_1560778,Human_Splice_Rec_1560779,Human_Splice_Rec_1560806,Human_Splice_Rec_1560807,Human_Splice_Rec_1560846,Human_Splice_Rec_1560847,Human_Splice_Rec_1560882,Human_Splice_Rec_1560883,Human_Splice_Rec_1560902,Human_Splice_Rec_1560903,Human_Splice_Rec_1560916,Human_Splice_Rec_1560917 Human_miRNA_ID_2018262,Human_miRNA_ID_2018263 RMVar_hsa_circ_41483,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_89665,RMVar_hsa_circ_101376,RMVar_hsa_circ_125927,RMVar_hsa_circ_92821,RMVar_hsa_circ_169663,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_169664,RMVar_hsa_circ_169662,RMVar_hsa_circ_369007 113551 RMVar_ID_113551 Human_SNP_ID_820985013 m1A Human chr14 - 74663532 74663532 74663532 GTCTTTACCTCACCTGCTCCCTGCCCATATCTACCACAGGCCACTTTGGCATGGTATGTAAGCTG GTCTTTACCTCACCTGCTCCCTGCCCATATCTCCCACAGGCCACTTTGGCATGGTATGTAAGCTG T G AREL1 Ensembl:ENSG00000119682 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1045430 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_19978857 Human_Splice_Rec_1535865 Human_miRNA_ID_1165884,Human_miRNA_ID_2846392,Human_miRNA_ID_2849413 GWAS_ID_8836,GWAS_ID_8837,GWAS_ID_8838,GWAS_ID_8839,GWAS_ID_8840,GWAS_ID_8841 RMVar_hsa_circ_75966,RMVar_hsa_circ_167926 113552 RMVar_ID_113552 Human_SNP_ID_820986615 m1A Human chr14 + 102348625 102348625 102348625 CTCCAGATGCAGCCTGCTGTCGCTCTCCACATAGGGCTGGTGCAGCCACATGGACAGGTAGCTCA CTCCAGATGCAGCCTGCTGTCGCTCTCCACATGGGGCTGGTGCAGCCACATGGACAGGTAGCTCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102348577..102348727 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 113553 RMVar_ID_113553 Human_SNP_ID_820988026 m1A Human chr14 + 19098431 19098431 19098431 CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGAAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG CAGGCGAGAGAGGCGGCCCGGTATCGATGGAGTAGCACAGAGGGCTTTGAGGTCGCAACGTCCCG A T DUXAP9 Ensembl:ENSG00000225210 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs865892571 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_17249243,Human_RBP_ID_17673155 113554 RMVar_ID_113554 Human_SNP_ID_821002887 m1A Human chr14 - 24432075 24432075 24432075 CTCCCACGCCTCTTCCCCAGGCAACTCCTTCCACCCCCAATCCATCTCCCTGGGACCACCCTGTT CTCCCACGCCTCTTCCCCAGGCAACTCCTTCCTCCCCCAATCCATCTCCCTGGGACCACCCTGTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:24432024..24432178;chr14:24431628..24432560 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 113555 RMVar_ID_113555 Human_SNP_ID_821034353 m1A Human chr14 + 61762606 61762606 61762606 CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCACCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA CGGGACTATCTTCTGGTGGGTGTTTCTTGTCCTCCACCCGCCTCTCCCTGCCCGCAGGTGGTGTA A T SNAPC1,AL137129.1 Ensembl:ENSG00000023608,Ensembl:ENSG00000258964 Protein coding,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:61762601..61762650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_19064091,Human_RBP_ID_27808918 113556 RMVar_ID_113556 Human_SNP_ID_821041546 m1A Human chr14 - 75657527 75657526 75657527 TCATGTCCTCTGCCTTTGTTTCCAAGGCAAAAAGCCCTCCCACGTTTGAGGGGAGTCATGAGCCG TCATGTCCTCTGCCTTTGTTTCCAAGGCAAAA_GCCCTCCCACGTTTGAGGGGAGTCATGAGCCG CT C ERG28 Ensembl:ENSG00000133935 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:75657476..75657559;chr14:75657476..75657571 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_4308015 Human_Splice_Rec_1537852 113557 RMVar_ID_113557 Human_SNP_ID_821065921 m1A Human chr14 + 21493064 21493064 21493064 GCAACAGCCTCCACCTCAGAAAGTTCGAATCAATTTACAGCAACAGCCTCCTCCTCTGCAGATCA GCAACAGCCTCCACCTCAGAAAGTTCGAATCAGTTTACAGCAACAGCCTCCTCCTCTGCAGATCA A G TOX4 Ensembl:ENSG00000092203 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:21493026..21493100 26863196 MeRIP-seq:(Medium) rs751970253 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_18980123,Human_RBP_ID_26922431 Human_miRNA_ID_1394787,Human_miRNA_ID_2715126,Human_miRNA_ID_3051109 RMVar_hsa_circ_165211,RMVar_hsa_circ_370024 113558 RMVar_ID_113558 Human_SNP_ID_821067355 m1A Human chr14 + 63727383 63727383 63727383 GTAGAAGACCTCCAACTTGACCACGGGCGGCGAGGCGGGCCTCGGCCAGCGGATGATGTCCTTGG GTAGAAGACCTCCAACTTGACCACGGGCGGCGCGGCGGGCCTCGGCCAGCGGATGATGTCCTTGG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:63727332..63727418 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 113559 RMVar_ID_113559 Human_SNP_ID_821074295 m1A Human chr14 + 24240873 24240873 24240873 CTCAGCCAGGTTCACTGAGTCAGTAACAGAGCACTCTGAAAAAGAAAATGAGGCCCCTTATAAAG CTCAGCCAGGTTCACTGAGTCAGTAACAGAGCCCTCTGAAAAAGAAAATGAGGCCCCTTATAAAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24240825..24241118 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 113560 RMVar_ID_113560 Human_SNP_ID_821077859 m1A Human chr14 - 100128569 100128569 100128569 GGGTGGGGGGGGCGGTGGAGGCCCACTACATGAGACGGGGGCGCTGGCTGCAGATGAAGGATGTC GGGTGGGGGGGGCGGTGGAGGCCCACTACATGCGACGGGGGCGCTGGCTGCAGATGAAGGATGTC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:100128490..100128792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach 113561 RMVar_ID_113561 Human_SNP_ID_821092493 m1A Human chr14 + 39179120 39179120 39179120 TAGCAAAAGCGGCGCCAGGAAATTGAACAAAAACTTGAAGTTCAGGCAGAAGAAGAGAGAAAGCA TAGCAAAAGCGGCGCCAGGAAATTGAACAAAAGCTTGAAGTTCAGGCAGAAGAAGAGAGAAAGCA A G PNN Ensembl:ENSG00000100941 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:39179086..39179362 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_445671,Human_RBP_ID_1493500,Human_RBP_ID_1818936,Human_RBP_ID_5563177,Human_RBP_ID_6347856,Human_RBP_ID_9041514,Human_RBP_ID_12329676,Human_RBP_ID_22797851,Human_RBP_ID_23621873,Human_RBP_ID_24543666,Human_RBP_ID_26924016 Human_Splice_Rec_1509348,Human_Splice_Rec_1509366 Human_miRNA_ID_196000,Human_miRNA_ID_696674,Human_miRNA_ID_701612,Human_miRNA_ID_1287396 RMVar_hsa_circ_124902,RMVar_hsa_circ_166121,RMVar_hsa_circ_166120,RMVar_hsa_circ_352048,RMVar_hsa_circ_166122,RMVar_hsa_circ_276099 113562 RMVar_ID_113562 Human_SNP_ID_821142576 m1A Human chr14 + 21074607 21074607 21074607 GCCACCGGAGACACCGGGCGTGGATGCACCAGAAGGGCCTGGGGCCTCGGGGCCAGGATGGAGCA GCCACCGGAGACACCGGGCGTGGATGCACCAGGAGGGCCTGGGGCCTCGGGGCCAGGATGGAGCA A G ARHGEF40 Ensembl:ENSG00000165801 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12889267 Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,rectum adenocarcinoma,large_intestine adenocarcinoma 2 caecum,large intestine Human_RBP_ID_5352613,Human_RBP_ID_5522570,Human_RBP_ID_22926382 GWAS_ID_13701,GWAS_ID_13702,GWAS_ID_13703,GWAS_ID_13704,GWAS_ID_13705,GWAS_ID_13706,GWAS_ID_13707,GWAS_ID_13708,GWAS_ID_13709,GWAS_ID_13710,GWAS_ID_13711,GWAS_ID_13712,GWAS_ID_13713,GWAS_ID_13714,GWAS_ID_13715,GWAS_ID_13716 RMVar_hsa_circ_78048,RMVar_hsa_circ_66452,RMVar_hsa_circ_109003,RMVar_hsa_circ_266567,RMVar_hsa_circ_165125,RMVar_hsa_circ_165126 113563 RMVar_ID_113563 Human_SNP_ID_821151599 m1A Human chr14 - 94801057 94801057 94801057 CCACATACAAATTTTTTGAGGTTATCCTCATTAATCCATTCCATAAAGCTATCAGAAGAAATCCT CCACATACAAATTTTTTGAGGTTATCCTCATTGATCCATTCCATAAAGCTATCAGAAGAAATCCT T C RPL15P2 Ensembl:ENSG00000240914 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 2 - 113564 RMVar_ID_113564 Human_SNP_ID_821151874 m1A Human chr14 - 100137646 100137646 100137646 GCCTCGCTGCTCAGGCCTTCCTGGGGCAGCTCACCTGGACAGAATCGAGGACACAGGCTTCTCCA GCCTCGCTGCTCAGGCCTTCCTGGGGCAGCTCGCCTGGACAGAATCGAGGACACAGGCTTCTCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr14:100137638..100137710;chr14:100137524..100137819 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113565 RMVar_ID_113565 Human_SNP_ID_821161782 m1A Human chr14 - 104714483 104714483 104714483 CTGGAGAACTTGAGGGGCTTCAGGGCCTGAGCATCTCCCAGAGTCACCGGCCAGGCCCCCTCCAA CTGGAGAACTTGAGGGGCTTCAGGGCCTGAGCGTCTCCCAGAGTCACCGGCCAGGCCCCCTCCAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:104714433..104714647 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113566 RMVar_ID_113566 Human_SNP_ID_821162637 m1A Human chr14 - 38209360 38209360 38209360 CATCCCAGCTGAGGGGGGCCAGTGGGGCTGCCAGGGCTGGGGCTTTCTCCTCGCGCACCCGCCGC CATCCCAGCTGAGGGGGGCCAGTGGGGCTGCCTGGGCTGGGGCTTTCTCCTCGCGCACCCGCCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:38209310..38209375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 113567 RMVar_ID_113567 Human_SNP_ID_821170771 m1A Human chr14 - 45134390 45134390 45134390 TGGAGCAGCTGCGCAGTGAGCAGCTGCCCAAGAAGGACATTATCAAGTTTCTGCAGGAACACGGT TGGAGCAGCTGCGCAGTGAGCAGCTGCCCAAGTAGGACATTATCAAGTTTCTGCAGGAACACGGT T A FKBP3 Ensembl:ENSG00000100442 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:45134368..45134461 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ORCA,mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_1493916,Human_RBP_ID_1819209,Human_RBP_ID_3449828,Human_RBP_ID_4308288,Human_RBP_ID_6349734,Human_RBP_ID_9368922,Human_RBP_ID_12332825,Human_RBP_ID_22926356,Human_RBP_ID_26324697,Human_RBP_ID_26924201 Human_Splice_Rec_1510677,Human_Splice_Rec_1510691,Human_Splice_Rec_1510703 113568 RMVar_ID_113568 Human_SNP_ID_821174068 m1A Human chr14 + 73569793 73569793 73569793 ACGACCCCGACCCCGGGCGGCTGCTGTGCCAGACGCGGCACGAGCGCTACTTCCTCCCGCCCGGG ACGACCCCGACCCCGGGCGGCTGCTGTGCCAGGCGCGGCACGAGCGCTACTTCCTCCCGCCCGGG A G ACOT2 Ensembl:ENSG00000119673 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73569685..73569845 26863196 MeRIP-seq:(Medium) rs1231350535 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_22439282 Human_Splice_Rec_1533897,Human_Splice_Rec_1533901,Human_Splice_Rec_1533905 RMVar_hsa_circ_167793,RMVar_hsa_circ_107415 113569 RMVar_ID_113569 Human_SNP_ID_821186182 m1A Human chr14 - 23322192 23322192 23322192 TCTTCCTCCATCTCCCTGACTCGAGCTTTGATAGCTTCCAGCTCCTAATATAAGTGGGGAGGGTA TCTTCCTCCATCTCCCTGACTCGAGCTTTGATTGCTTCCAGCTCCTAATATAAGTGGGGAGGGTA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:23322182..23322283 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113570 RMVar_ID_113570 Human_SNP_ID_821192947 m1A Human chr14 - 49633812 49633812 49633812 GGGGAGCAGGACTTGAGCAGGCACGCGGGGTCACCGCCGGGCAGCGTGGAGGAGCCATCTCCTGG GGGGAGCAGGACTTGAGCAGGCACGCGGGGTCGCCGCCGGGCAGCGTGGAGGAGCCATCTCCTGG T C DNAAF2 Ensembl:ENSG00000165506 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr14:49633797..49633946;chr14:49633639..49633941 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_883637,Human_RBP_ID_4308766,Human_RBP_ID_22045256 RMVar_hsa_circ_76409,RMVar_hsa_circ_114563,RMVar_hsa_circ_166277,RMVar_hsa_circ_118194,RMVar_hsa_circ_99000,RMVar_hsa_circ_87204,RMVar_hsa_circ_166284,RMVar_hsa_circ_166285,RMVar_hsa_circ_166286,RMVar_hsa_circ_123309,RMVar_hsa_circ_120257,RMVar_hsa_circ_82953,RMVar_hsa_circ_84908,RMVar_hsa_circ_166291,RMVar_hsa_circ_166293,RMVar_hsa_circ_166294,RMVar_hsa_circ_166292,RMVar_hsa_circ_166290 113571 RMVar_ID_113571 Human_SNP_ID_821193634 m1A Human chr14 + 72940305 72940304 72940306 CCTGGACATAACAACTGCAACCCCCTGACGAAAGAGAGCATCCGGCAGAAGGAGATGGAGAGCAA CCTGGACATAACAACTGCAACCCCCTGACGAA__AGAGCATCCGGCAGAAGGAGATGGAGAGCAA AAG A DCAF4 Ensembl:ENSG00000119599 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:72940190..72940372 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - Human_RBP_ID_18980776,Human_RBP_ID_26325193 Human_Splice_Rec_1532234,Human_Splice_Rec_1532235,Human_Splice_Rec_1532246,Human_Splice_Rec_1532247,Human_Splice_Rec_1532270,Human_Splice_Rec_1532271,Human_Splice_Rec_1532294,Human_Splice_Rec_1532295,Human_Splice_Rec_1532318,Human_Splice_Rec_1532319,Human_Splice_Rec_1532338,Human_Splice_Rec_1532339,Human_Splice_Rec_1532360,Human_Splice_Rec_1532364,Human_Splice_Rec_1532365,Human_Splice_Rec_1532372,Human_Splice_Rec_1532376,Human_Splice_Rec_1532377,Human_Splice_Rec_1532382,Human_Splice_Rec_1532383,Human_Splice_Rec_1532386,Human_Splice_Rec_1532387 RMVar_hsa_circ_18779,RMVar_hsa_circ_39916,RMVar_hsa_circ_126731,RMVar_hsa_circ_287632,RMVar_hsa_circ_167724,RMVar_hsa_circ_167725,RMVar_hsa_circ_23204 113572 RMVar_ID_113572 Human_SNP_ID_821214020 m1A Human chr14 + 21093640 21093639 21093640 CTTTGGTTCTGGGAAGTGCAGGGAAGAGGAGGAAAAGCTGCTAATGAAGGCAACAGGTGCTGTGG CTTTGGTTCTGGGAAGTGCAGGGAAGAGGAGG_AAAGCTGCTAATGAAGGCAACAGGTGCTGTGG GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21093577..21093728 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 COAD 1 - 113573 RMVar_ID_113573 Human_SNP_ID_821217219 m1A Human chr14 + 102010912 102010912 102010912 GAAGAAAGTGTGTCAGGAGATGTATTTGACATATGGAGATGGAGAAGAAGTTGGTGGAATGTGGG GAAGAAAGTGTGTCAGGAGATGTATTTGACATTTGGAGATGGAGAAGAAGTTGGTGGAATGTGGG A T DYNC1H1 Ensembl:ENSG00000197102 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:102010826..102010996 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_1814474,Human_RBP_ID_4309754,Human_RBP_ID_5562910,Human_RBP_ID_8792557,Human_RBP_ID_17478223,Human_RBP_ID_17856508,Human_RBP_ID_22920974,Human_RBP_ID_23611531 Human_Splice_Rec_1555789,Human_Splice_Rec_1555903,Human_Splice_Rec_1555959,Human_Splice_Rec_1555979 Human_miRNA_ID_1539945,Human_miRNA_ID_1593841 RMVar_hsa_circ_2890,RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_105470,RMVar_hsa_circ_112765,RMVar_hsa_circ_103313,RMVar_hsa_circ_169157,RMVar_hsa_circ_169159,RMVar_hsa_circ_169158,RMVar_hsa_circ_124549,RMVar_hsa_circ_119991,RMVar_hsa_circ_169165,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_121278,RMVar_hsa_circ_8271,RMVar_hsa_circ_83551,RMVar_hsa_circ_169168,RMVar_hsa_circ_77296,RMVar_hsa_circ_169174,RMVar_hsa_circ_106610,RMVar_hsa_circ_87006,RMVar_hsa_circ_87310,RMVar_hsa_circ_169176,RMVar_hsa_circ_169177,RMVar_hsa_circ_89234,RMVar_hsa_circ_122969,RMVar_hsa_circ_169179,RMVar_hsa_circ_169178,RMVar_hsa_circ_102363,RMVar_hsa_circ_119186,RMVar_hsa_circ_169184,RMVar_hsa_circ_81731,RMVar_hsa_circ_85393,RMVar_hsa_circ_169185,RMVar_hsa_circ_169186,RMVar_hsa_circ_169182,RMVar_hsa_circ_169183,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_120327,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,RMVar_hsa_circ_169201,RMVar_hsa_circ_169199,RMVar_hsa_circ_106225,RMVar_hsa_circ_114900,RMVar_hsa_circ_169206,RMVar_hsa_circ_90279,RMVar_hsa_circ_99123,RMVar_hsa_circ_77743,RMVar_hsa_circ_87202,RMVar_hsa_circ_169207,RMVar_hsa_circ_169209,RMVar_hsa_circ_169210,RMVar_hsa_circ_169208,RMVar_hsa_circ_118022,RMVar_hsa_circ_97713,RMVar_hsa_circ_100507,RMVar_hsa_circ_96241,RMVar_hsa_circ_114823,RMVar_hsa_circ_169214,RMVar_hsa_circ_81418,RMVar_hsa_circ_169216,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_169215,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_103508,RMVar_hsa_circ_28807,RMVar_hsa_circ_80975,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169223,RMVar_hsa_circ_169221,RMVar_hsa_circ_117510,RMVar_hsa_circ_105884,RMVar_hsa_circ_70271,RMVar_hsa_circ_77475,RMVar_hsa_circ_28908,RMVar_hsa_circ_114068,RMVar_hsa_circ_169225,RMVar_hsa_circ_169227,RMVar_hsa_circ_169229,RMVar_hsa_circ_169228,RMVar_hsa_circ_169226,RMVar_hsa_circ_126338,RMVar_hsa_circ_80911,RMVar_hsa_circ_101542,RMVar_hsa_circ_76343,RMVar_hsa_circ_112723,RMVar_hsa_circ_169231,RMVar_hsa_circ_169233,RMVar_hsa_circ_169234,RMVar_hsa_circ_169232,RMVar_hsa_circ_169230,RMVar_hsa_circ_111597,RMVar_hsa_circ_169237,RMVar_hsa_circ_27120,RMVar_hsa_circ_2934,RMVar_hsa_circ_114571,RMVar_hsa_circ_118470,RMVar_hsa_circ_169238,RMVar_hsa_circ_169239,RMVar_hsa_circ_169240,RMVar_hsa_circ_344683,RMVar_hsa_circ_98599,RMVar_hsa_circ_93924,RMVar_hsa_circ_169241,RMVar_hsa_circ_113112,RMVar_hsa_circ_97684,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_94660,RMVar_hsa_circ_79959,RMVar_hsa_circ_121747,RMVar_hsa_circ_169247,RMVar_hsa_circ_169248,RMVar_hsa_circ_169251,RMVar_hsa_circ_82924,RMVar_hsa_circ_113873,RMVar_hsa_circ_169252,RMVar_hsa_circ_169253,RMVar_hsa_circ_125165,RMVar_hsa_circ_77200,RMVar_hsa_circ_126755,RMVar_hsa_circ_169257,RMVar_hsa_circ_169258,RMVar_hsa_circ_328465,RMVar_hsa_circ_360611,RMVar_hsa_circ_169256,RMVar_hsa_circ_345503,RMVar_hsa_circ_58723,RMVar_hsa_circ_125284,RMVar_hsa_circ_39229,RMVar_hsa_circ_124056,RMVar_hsa_circ_79196,RMVar_hsa_circ_115872,RMVar_hsa_circ_125913,RMVar_hsa_circ_169259,RMVar_hsa_circ_169260,RMVar_hsa_circ_83725,RMVar_hsa_circ_169261,RMVar_hsa_circ_169263,RMVar_hsa_circ_169264,RMVar_hsa_circ_169262,RMVar_hsa_circ_127543,RMVar_hsa_circ_81152,RMVar_hsa_circ_115030,RMVar_hsa_circ_169267,RMVar_hsa_circ_169269,RMVar_hsa_circ_117196,RMVar_hsa_circ_169268,RMVar_hsa_circ_111075,RMVar_hsa_circ_169270,RMVar_hsa_circ_169271,RMVar_hsa_circ_45006,RMVar_hsa_circ_169272 113574 RMVar_ID_113574 Human_SNP_ID_821235342 m1A Human chr14 + 68793008 68793005 68793008 GTGTCGCGAAGGTCCCGGTGCGGGGAAGGCGCAGCCTCTCCTGTCTGGAGTCCCACACGCCAGTT GTGTCGCGAAGGTCCCGGTGCGGGGAAGGC___GCCTCTCCTGTCTGGAGTCCCACACGCCAGTT CGCA C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:68792841..68793080 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 ESCA 1 - 113575 RMVar_ID_113575 Human_SNP_ID_821321416 m1A Human chr14 - 66013441 66013441 66013441 AGTTTGATGTTGTTGAAGGAGAAAAGGGTGCGAAGGCAGCAAATGTTACAGGTCCTGGTGGTGTT AGTTTGATGTTGTTGAAGGAGAAAAGGGTGCGGAGGCAGCAAATGTTACAGGTCCTGGTGGTGTT T C YBX1P1 Ensembl:ENSG00000224861 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs878979795 Functional Loss SNV TCGA,ICGC 33..33 33 LAML,LUSC 3 - Human_RBP_ID_6402910,Human_RBP_ID_17857119 113576 RMVar_ID_113576 Human_SNP_ID_821336873 m1A Human chr14 + 22767377 22767377 22767377 TCTTCCTTGCGGCTTCCGGCCCCCGCAGCCTCAGTACCTCTGCTATCTCTTTTGCAGAAGTCCAG TCTTCCTTGCGGCTTCCGGCCCCCGCAGCCTCGGTACCTCTGCTATCTCTTTTGCAGAAGTCCAG A G OXA1L Ensembl:ENSG00000155463 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:22767326..22767467 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_231250,Human_RBP_ID_757258,Human_RBP_ID_813657,Human_RBP_ID_8401825,Human_RBP_ID_9323726,Human_RBP_ID_17481025,Human_RBP_ID_17846338,Human_RBP_ID_24471088 Human_Splice_Rec_1492829,Human_Splice_Rec_1492847,Human_Splice_Rec_1492853,Human_Splice_Rec_1492859,Human_Splice_Rec_1492876,Human_Splice_Rec_1492877,Human_Splice_Rec_1492887,Human_Splice_Rec_1492897,Human_Splice_Rec_1492913,Human_Splice_Rec_1492929,Human_Splice_Rec_1492947,Human_Splice_Rec_1492949 Human_miRNA_ID_1394790,Human_miRNA_ID_2273187,Human_miRNA_ID_2715130,Human_miRNA_ID_3051113 RMVar_hsa_circ_165220,RMVar_hsa_circ_117680,RMVar_hsa_circ_125634,RMVar_hsa_circ_165221 113577 RMVar_ID_113577 Human_SNP_ID_821341923 m1A Human chr14 + 19075237 19075237 19075237 TAGATTCAGTGTCAGCTATGACAATTGAAAATAAGCTGTTTTGTGATTTAAAGGTTTAAATTTCT TAGATTCAGTGTCAGCTATGACAATTGAAAATGAGCTGTTTTGTGATTTAAAGGTTTAAATTTCT A G AL589182.3,DUXAP9 Ensembl:ENSG00000286614,Ensembl:ENSG00000225210 Pseudogene,Pseudogene exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs768451165 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 113578 RMVar_ID_113578 Human_SNP_ID_821342021 m1A Human chr14 + 65102455 65102372 65102455 AAGCCGAGTCCCCCCCACACACACACTCACTCACTCACTCACTCGCTCTCTCACTCACACACACA _________________________________CTCACTCACTCGCTCTCTCACTCACACACACA GCGGCGGGGAGGGGAAGGGGTGAAGGGGAGGGGGAAGTCACCGACAACAACAAGCCGAGTCCCCCCCACACACACACTCACTCA G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr14:65102354..65102466 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 1..33 33 BRCA 1 - 113579 RMVar_ID_113579 Human_SNP_ID_821369305 m1A Human chr14 - 34996775 34996775 34996775 TCATACAATATTTTACATACCTCTTCATTGATAATGGTGGCATTGCTCAACGAGCGTAATGCTGA TCATACAATATTTTACATACCTCTTCATTGATTATGGTGGCATTGCTCAACGAGCGTAATGCTGA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:34996751..34996775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 113580 RMVar_ID_113580 Human_SNP_ID_821412025 m1A Human chr14 + 70010797 70010797 70010797 TCGTGTGACCAGGAGAGGCAGAGTGCCCTGGAAGAGGCCCAGCAGAATCCCCGTGAGGGTATTGT TCGTGTGACCAGGAGAGGCAGAGTGCCCTGGAGGAGGCCCAGCAGAATCCCCGTGAGGGTATTGT A G SMOC1 Ensembl:ENSG00000198732 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:70010713..70010987 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_450790,Human_RBP_ID_18979731,Human_RBP_ID_22438775 Human_Splice_Rec_1530402,Human_Splice_Rec_1530424,Human_Splice_Rec_1530440 RMVar_hsa_circ_78270,RMVar_hsa_circ_26410,RMVar_hsa_circ_59463,RMVar_hsa_circ_278946,RMVar_hsa_circ_291619,RMVar_hsa_circ_113137,RMVar_hsa_circ_167544,RMVar_hsa_circ_167543,RMVar_hsa_circ_167549,RMVar_hsa_circ_89645,RMVar_hsa_circ_167550,RMVar_hsa_circ_167548,RMVar_hsa_circ_323721,RMVar_hsa_circ_333915,RMVar_hsa_circ_95898,RMVar_hsa_circ_167552,RMVar_hsa_circ_167554,RMVar_hsa_circ_167553,RMVar_hsa_circ_167555,RMVar_hsa_circ_79835,RMVar_hsa_circ_167556,RMVar_hsa_circ_280496,RMVar_hsa_circ_354555,RMVar_hsa_circ_167557 113581 RMVar_ID_113581 Human_SNP_ID_821412130 m1A Human chr14 + 99850897 99850897 99850897 CTGCTGCAAGTAGCATGGAGGTGACAGACCGCATTGCTTCACTGGAGCAGAGAGTCCAGATGCAA CTGCTGCAAGTAGCATGGAGGTGACAGACCGCGTTGCTTCACTGGAGCAGAGAGTCCAGATGCAA A G EML1 Ensembl:ENSG00000066629 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:99850808..99850896 26863196 MeRIP-seq:(Medium) rs376349469 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 3 biliary tract,gallbladder Human_RBP_ID_1487341 Human_Splice_Rec_1552294,Human_Splice_Rec_1552314,Human_Splice_Rec_1552322,Human_Splice_Rec_1552366,Human_Splice_Rec_1552372,Human_Splice_Rec_1552416,Human_Splice_Rec_1552422,Human_Splice_Rec_1552466,Human_Splice_Rec_1552472,Human_Splice_Rec_1552514,Human_Splice_Rec_1552530,Human_Splice_Rec_1552536 RMVar_hsa_circ_168977,RMVar_hsa_circ_110014,RMVar_hsa_circ_168974,RMVar_hsa_circ_168973,RMVar_hsa_circ_168975,RMVar_hsa_circ_31947,RMVar_hsa_circ_13783,RMVar_hsa_circ_277283,RMVar_hsa_circ_307494,RMVar_hsa_circ_168976,RMVar_hsa_circ_331986,RMVar_hsa_circ_279906,RMVar_hsa_circ_265741,RMVar_hsa_circ_168978,RMVar_hsa_circ_168980,RMVar_hsa_circ_168981,RMVar_hsa_circ_168979 113582 RMVar_ID_113582 Human_SNP_ID_821439206 m1A Human chr14 - 93240209 93240209 93240209 TGGTTAGCTGCTGTGCGGGTGCGCTCGGTGACACTGGTGGTGGTGCACGCTCCCGAGCTCCCAGA TGGTTAGCTGCTGTGCGGGTGCGCTCGGTGACGCTGGTGGTGGTGCACGCTCCCGAGCTCCCAGA T C BTBD7 Ensembl:ENSG00000011114 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8013451 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_6396879 Human_miRNA_ID_504436,Human_miRNA_ID_511649,Human_miRNA_ID_2175446,Human_miRNA_ID_2178889 GWAS_ID_7368,GWAS_ID_7369 RMVar_hsa_circ_106641,RMVar_hsa_circ_110334,RMVar_hsa_circ_168727,RMVar_hsa_circ_168729,RMVar_hsa_circ_94171,RMVar_hsa_circ_168728 113583 RMVar_ID_113583 Human_SNP_ID_821440686 m1A Human chr14 - 104175605 104175605 104175605 CTGGGCAGTGGCCTCCTGCCTCCACTCACTGCAGCCTTTTCCGGGACCAGCAGCTCAGGCCAAGC CTGGGCAGTGGCCTCCTGCCTCCACTCACTGCGGCCTTTTCCGGGACCAGCAGCTCAGGCCAAGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr14:104175460..104175724;chr14:104174981..104175833 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 113584 RMVar_ID_113584 Human_SNP_ID_821457290 m1A Human chr14 - 74942086 74942086 74942086 TTGCTTGTACTGGGACATTGTTCTTTCCGGCCAAGGTGCCACCACCCTGCCCCCCCTAAGAGACA TTGCTTGTACTGGGACATTGTTCTTTCCGGCCGAGGTGCCACCACCCTGCCCCCCCTAAGAGACA T C PGF Ensembl:ENSG00000119630 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8185 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_451878,Human_RBP_ID_5112726,Human_RBP_ID_27559167 GWAS_ID_8842,GWAS_ID_8843,GWAS_ID_8844,GWAS_ID_8845,GWAS_ID_8846,GWAS_ID_8847,GWAS_ID_8848 113585 RMVar_ID_113585 Human_SNP_ID_821473279 m1A Human chr14 - 77275051 77275051 77275051 GGTGGAGGAAGAAGATGTTCGTCAGCCAATTCAACCTCCAGCCAGCTTCTTGAGCCTATTTGGTT GGTGGAGGAAGAAGATGTTCGTCAGCCAATTCGACCTCCAGCCAGCTTCTTGAGCCTATTTGGTT T C POMT2 Ensembl:ENSG00000009830 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11547793 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Clinvar_Rec_337 GWAS_ID_8921,GWAS_ID_8922 113586 RMVar_ID_113586 Human_SNP_ID_821487893 m1A Human chr14 + 75470019 75470019 75470019 CCCACCCACCTCGGTCCAGCGCGGCCCTGCCCAGGAGGCGGCAGCCGGGCGCACCCTCGCCAGCC CCCACCCACCTCGGTCCAGCGCGGCCCTGCCCCGGAGGCGGCAGCCGGGCGCACCCTCGCCAGCC A C JDP2 Ensembl:ENSG00000140044 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:75469968..75470096 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_miRNA_ID_253685,Human_miRNA_ID_2040558,Human_miRNA_ID_3019538 RMVar_hsa_circ_82507,RMVar_hsa_circ_168027 113587 RMVar_ID_113587 Human_SNP_ID_821491008 m1A Human chr14 - 73712624 73712621 73712624 CCGTGAGGAGGAAGCCAAGGAGGAGGAGGAGGAGGCTGAGGCCACCCTTCTGCAGTTAGGCCTGG CCGTGAGGAGGAAGCCAAGGAGGAGGAGGAGG___CTGAGGCCACCCTTCTGCAGTTAGGCCTGG GCCT G PNMA1 Ensembl:ENSG00000176903 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73712601..73712625 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..35 33 PRAD,UCEC 2 - Human_RBP_ID_6382962 113588 RMVar_ID_113588 Human_SNP_ID_821513463 m1A Human chr14 - 69384903 69384903 69384903 GGCCAAGAGAGGGTAGGAGATGAGATCATTAGAGGAAAAGACTTCATGGAATTGGGAGGCCTAAG GGCCAAGAGAGGGTAGGAGATGAGATCATTAGGGGAAAAGACTTCATGGAATTGGGAGGCCTAAG T C ERH Ensembl:ENSG00000100632 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:69384900..69384994 26863196 MeRIP-seq:(Medium) rs1391681014 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_12398820 RMVar_hsa_circ_98800,RMVar_hsa_circ_122006,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167515,RMVar_hsa_circ_167514 113589 RMVar_ID_113589 Human_SNP_ID_821525731 m1A Human chr14 + 104776708 104776708 104776708 CACATGGAAGGTGCGTTCGATGACAGTGGTCCACTGCAGGCAGCGGATGATGAAGGTGTTGGGCC CACATGGAAGGTGCGTTCGATGACAGTGGTCCGCTGCAGGCAGCGGATGATGAAGGTGTTGGGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr14:104776631..104776725;chr14:104776651..104776825 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,prostate adenocarcinoma,breast ductal_carcinoma,caecum adenocarcinoma,UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 53 caecum,uterus,prostate,large intestine,breast 113590 RMVar_ID_113590 Human_SNP_ID_821525739 m1A Human chr14 + 104776708 104776708 104776708 CACATGGAAGGTGCGTTCGATGACAGTGGTCCACTGCAGGCAGCGGATGATGAAGGTGTTGGGCC CACATGGAAGGTGCGTTCGATGACAGTGGTCCTCTGCAGGCAGCGGATGATGAAGGTGTTGGGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr14:104776631..104776725;chr14:104776651..104776825 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary granulosa_cell_tumour 6 ovary 113591 RMVar_ID_113591 Human_SNP_ID_821541714 m1A Human chr14 - 96502576 96502576 96502576 TTACTTACAACGGCATCGTCTCCGGCGCCGGCACCGCCCAGTCACTTCCCCCCCGCAACCGCCGC TTACTTACAACGGCATCGTCTCCGGCGCCGGCGCCGCCCAGTCACTTCCCCCCCGCAACCGCCGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:96502476..96502642 26863410 MeRIP-seq:(Medium) rs776518436 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 113592 RMVar_ID_113592 Human_SNP_ID_821553151 m1A Human chr14 + 104166969 104166969 104166969 CACCTACCCCACCGACTTCAGCGGGGTCCTGCAGCTGTGGCCGCCCCCGGCGCCCCCCTGCCTGC CACCTACCCCACCGACTTCAGCGGGGTCCTGCGGCTGTGGCCGCCCCCGGCGCCCCCCTGCCTGC A G KIF26A Ensembl:ENSG00000066735 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104166918..104166997 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_Splice_Rec_1560189,Human_Splice_Rec_1560215 Human_miRNA_ID_1998527,Human_miRNA_ID_2387022,Human_miRNA_ID_2388497,Human_miRNA_ID_2399645,Human_miRNA_ID_3030701 RMVar_hsa_circ_116512,RMVar_hsa_circ_318351,RMVar_hsa_circ_304944,RMVar_hsa_circ_169631 113593 RMVar_ID_113593 Human_SNP_ID_821557381 m1A Human chr14 - 22767352 22767352 22767352 GAGGTACTGAGGCTGCGGGGGCCGGAAGCCGCAAGGAAGAGGTAGTGTGGGCGACAGCAGCACGG GAGGTACTGAGGCTGCGGGGGCCGGAAGCCGCGAGGAAGAGGTAGTGTGGGCGACAGCAGCACGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:22767301..22767400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 113594 RMVar_ID_113594 Human_SNP_ID_821572264 m1A Human chr14 + 33039778 33039778 33039778 AAGTGCAAGCTCCTCTATTATTAAACACTTTCAATAGCAGGCATGGTACATGTGCAGACTGCACA AAGTGCAAGCTCCTCTATTATTAAACACTTTCGATAGCAGGCATGGTACATGTGCAGACTGCACA A G NPAS3 Ensembl:ENSG00000151322 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:33039658..33039788 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate 113595 RMVar_ID_113595 Human_SNP_ID_821635922 m1A Human chr14 + 70375692 70375692 70375692 TCAAAGTGATACCTACCCTGTGCTGCACTCTCAGAGACACAGCATAGCCTGCATTACGAAAGAGG TCAAAGTGATACCTACCCTGTGCTGCACTCTCGGAGACACAGCATAGCCTGCATTACGAAAGAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:70373006..70375696 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113596 RMVar_ID_113596 Human_SNP_ID_821637803 m1A Human chr14 - 88563658 88563658 88563658 CATAAGCTCCTAATTCTTGTAATTTCCCCTTAATGGCACTCTGAGAGAAAAAGAGCAAACGTGCA CATAAGCTCCTAATTCTTGTAATTTCCCCTTAGTGGCACTCTGAGAGAAAAAGAGCAAACGTGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:88563651..88563700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 9 large intestine 113597 RMVar_ID_113597 Human_SNP_ID_821645613 m1A Human chr14 - 104785983 104785983 104785983 GAGGGGTGGGTGACGGGCAGTGCCTGTGGGGGAGGACATCCAGGCCCAGGTGGTCTGTCAGGGGC GAGGGGTGGGTGACGGGCAGTGCCTGTGGGGGGGGACATCCAGGCCCAGGTGGTCTGTCAGGGGC T C AKT1 Ensembl:ENSG00000142208 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:104785971..104786121 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_260722,Human_RBP_ID_1065742,Human_RBP_ID_2407540,Human_RBP_ID_3468340,Human_RBP_ID_5177704,Human_RBP_ID_5645883,Human_RBP_ID_8078403,Human_RBP_ID_8181140,Human_RBP_ID_8230592,Human_RBP_ID_8725856,Human_RBP_ID_9324157,Human_RBP_ID_9353026,Human_RBP_ID_9417971,Human_RBP_ID_18418227,Human_RBP_ID_18457754,Human_RBP_ID_18480739,Human_RBP_ID_22355078,Human_RBP_ID_22415068,Human_RBP_ID_22711206,Human_RBP_ID_22737409,Human_RBP_ID_23272490,Human_RBP_ID_26778238,Human_RBP_ID_27837273 RMVar_hsa_circ_19812,RMVar_hsa_circ_372085,RMVar_hsa_circ_87438,RMVar_hsa_circ_169658,RMVar_hsa_circ_169657,RMVar_hsa_circ_125927,RMVar_hsa_circ_169665,RMVar_hsa_circ_80208,RMVar_hsa_circ_169666,RMVar_hsa_circ_369007 113598 RMVar_ID_113598 Human_SNP_ID_821646949 m1A Human chr14 - 64986996 64986996 64986996 ACTGTACAGCGGCTCTGACCAGACGGGGGAGGAAGATGGAGGGCAATAGTAGGTGAAAGAACTCG ACTGTACAGCGGCTCTGACCAGACGGGGGAGGCAGATGGAGGGCAATAGTAGGTGAAAGAACTCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:64986947..64987039 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - 113599 RMVar_ID_113599 Human_SNP_ID_821647095 m1A Human chr14 + 21391510 21391510 21391510 ATCAACAGCAAACTCTGGATGACCCTGTAACCACATCTCCAGTTCAGCCCGGCGAGGGGCATCCT ATCAACAGCAAACTCTGGATGACCCTGTAACCGCATCTCCAGTTCAGCCCGGCGAGGGGCATCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21391501..21391525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113600 RMVar_ID_113600 Human_SNP_ID_821650181 m1A Human chr14 - 64951642 64951641 64951643 TTCTCCTGCAGGGACACTGCAGGGCAGGAGAGATACCAGACCATCACAAAGCAGTACTATCGGCG TTCTCCTGCAGGGACACTGCAGGGCAGGAGA__TACCAGACCATCACAAAGCAGTACTATCGGCG ATC A RAB15 Ensembl:ENSG00000139998 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64951141..64957957 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - Human_Splice_Rec_1526346,Human_Splice_Rec_1526347,Human_Splice_Rec_1526360,Human_Splice_Rec_1526361,Human_Splice_Rec_1526372,Human_Splice_Rec_1526373,Human_Splice_Rec_1526384,Human_Splice_Rec_1526385,Human_Splice_Rec_1526398,Human_Splice_Rec_1526399,Human_Splice_Rec_1526414,Human_Splice_Rec_1526415,Human_Splice_Rec_1526428,Human_Splice_Rec_1526429,Human_Splice_Rec_1526438,Human_Splice_Rec_1526439,Human_Splice_Rec_1526450,Human_Splice_Rec_1526451 RMVar_hsa_circ_37271,RMVar_hsa_circ_167324,RMVar_hsa_circ_110583 113601 RMVar_ID_113601 Human_SNP_ID_821653094 m1A Human chr14 - 45129877 45129877 45129877 CCTTACAGCGTTTTAAGGGTACTGAAAGTATAAGTAAAGTGTCTGAGCAAGTAAAAAATGTGAAG CCTTACAGCGTTTTAAGGGTACTGAAAGTATAGGTAAAGTGTCTGAGCAAGTAAAAAATGTGAAG T C FKBP3 Ensembl:ENSG00000100442 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:45129826..45129925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder Human_RBP_ID_40640,Human_RBP_ID_1819182,Human_RBP_ID_3449810,Human_RBP_ID_9041859,Human_RBP_ID_23622792,Human_RBP_ID_24543842 Human_Splice_Rec_1510680,Human_Splice_Rec_1510681,Human_Splice_Rec_1510694,Human_Splice_Rec_1510695,Human_Splice_Rec_1510708,Human_Splice_Rec_1510709,Human_Splice_Rec_1510714,Human_Splice_Rec_1510715 RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231,RMVar_hsa_circ_302555,RMVar_hsa_circ_166232,RMVar_hsa_circ_353106 113602 RMVar_ID_113602 Human_SNP_ID_821664974 m1A Human chr14 - 74486401 74486401 74486401 CTGTGGATGGAGTTATAAAGGAAGTGAATGTGAGCCCATGCCCCACCCAACCCTGCCAGCTGAGC CTGTGGATGGAGTTATAAAGGAAGTGAATGTGCGCCCATGCCCCACCCAACCCTGCCAGCTGAGC T G NPC2 Ensembl:ENSG00000119655 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:74486280..74486491 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 6 oesophagus Human_RBP_ID_451690,Human_RBP_ID_756514,Human_RBP_ID_883834,Human_RBP_ID_1824268,Human_RBP_ID_4308418,Human_RBP_ID_5112415,Human_RBP_ID_5140888,Human_RBP_ID_12419318,Human_RBP_ID_22439289,Human_RBP_ID_22758177,Human_RBP_ID_23636241 Human_Splice_Rec_1535552,Human_Splice_Rec_1535553,Human_Splice_Rec_1535560,Human_Splice_Rec_1535561,Human_Splice_Rec_1535566,Human_Splice_Rec_1535567,Human_Splice_Rec_1535574,Human_Splice_Rec_1535575,Human_Splice_Rec_1535580,Human_Splice_Rec_1535581,Human_Splice_Rec_1535588,Human_Splice_Rec_1535589,Human_Splice_Rec_1535596,Human_Splice_Rec_1535597,Human_Splice_Rec_1535604,Human_Splice_Rec_1535605,Human_Splice_Rec_1535612,Human_Splice_Rec_1535613 Human_miRNA_ID_216400,Human_miRNA_ID_2022429,Human_miRNA_ID_2260971,Human_miRNA_ID_2264017,Human_miRNA_ID_2267084,Human_miRNA_ID_2493476 RMVar_hsa_circ_16293,RMVar_hsa_circ_126898,RMVar_hsa_circ_167867 113603 RMVar_ID_113603 Human_SNP_ID_821675704 m1A Human chr14 - 102081806 102081806 102081806 TTTTATTTTGGAAACAGGTATTGATGAAGATGACCCTACTGCTGATGATACCAGTGCTGCTGTAA TTTTATTTTGGAAACAGGTATTGATGAAGATGGCCCTACTGCTGATGATACCAGTGCTGCTGTAA T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:102081708..102081834 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_882686,Human_RBP_ID_1487943,Human_RBP_ID_1814594,Human_RBP_ID_2405390,Human_RBP_ID_5112470,Human_RBP_ID_6324541,Human_RBP_ID_9369439,Human_RBP_ID_12270912,Human_RBP_ID_17361385,Human_RBP_ID_17478257,Human_RBP_ID_18645129,Human_RBP_ID_22495021,Human_RBP_ID_23611617,Human_RBP_ID_25082883,Human_RBP_ID_26324741,Human_RBP_ID_26427185 Human_Splice_Rec_1556706,Human_Splice_Rec_1556728 RMVar_hsa_circ_96094,RMVar_hsa_circ_117634,RMVar_hsa_circ_119021,RMVar_hsa_circ_120437,RMVar_hsa_circ_127877,RMVar_hsa_circ_119531,RMVar_hsa_circ_117744,RMVar_hsa_circ_108825,RMVar_hsa_circ_110324,RMVar_hsa_circ_102877,RMVar_hsa_circ_169370,RMVar_hsa_circ_169374,RMVar_hsa_circ_87088,RMVar_hsa_circ_87280,RMVar_hsa_circ_169376,RMVar_hsa_circ_169378,RMVar_hsa_circ_169379,RMVar_hsa_circ_169377,RMVar_hsa_circ_169375,RMVar_hsa_circ_169372,RMVar_hsa_circ_169373,RMVar_hsa_circ_169371,RMVar_hsa_circ_169368,RMVar_hsa_circ_169369 113604 RMVar_ID_113604 Human_SNP_ID_821683822 m1A Human chr14 + 73592297 73592297 73592297 TGTCGTGGAGTTGGAGGTGCTGGACGGCCACGACCCCGAGCCTGGACGGCTGCTGTGCCAGGCGC TGTCGTGGAGTTGGAGGTGCTGGACGGCCACGCCCCCGAGCCTGGACGGCTGCTGTGCCAGGCGC A C ACOT4 Ensembl:ENSG00000177465 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:73592193..73592339 26863196 MeRIP-seq:(Medium) rs768965606 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 1 lung 113605 RMVar_ID_113605 Human_SNP_ID_821705967 m1A Human chr14 + 68789460 68789460 68789460 TTAATGTAGGGCCTGTGGGGAATGGGATGGGTAGGGAGAAGAGGGTATGGGATGTGGGTGCAGGG TTAATGTAGGGCCTGTGGGGAATGGGATGGGTGGGGAGAAGAGGGTATGGGATGTGGGTGCAGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:68789411..68789525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney 113606 RMVar_ID_113606 Human_SNP_ID_821713411 m1A Human chr14 + 49620869 49620869 49620869 GGCGAGGCCGCGTCGCTCAGTTCTGGCCGTCTAGGGCCCCTGTAAGGATGAGAGCGCAGAGGACG GGCGAGGCCGCGTCGCTCAGTTCTGGCCGTCTGGGGCCCCTGTAAGGATGAGAGCGCAGAGGACG A G MGAT2 Ensembl:ENSG00000168282 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:49620822..49621050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_757351,Human_RBP_ID_1494144,Human_RBP_ID_4307903,Human_RBP_ID_5463385,Human_RBP_ID_9042130 RMVar_hsa_circ_126072,RMVar_hsa_circ_166283,RMVar_hsa_circ_82963,RMVar_hsa_circ_166282,RMVar_hsa_circ_80380,RMVar_hsa_circ_98401,RMVar_hsa_circ_97340,RMVar_hsa_circ_166287,RMVar_hsa_circ_166289,RMVar_hsa_circ_79226,RMVar_hsa_circ_166288,RMVar_hsa_circ_166296,RMVar_hsa_circ_105642,RMVar_hsa_circ_122603,RMVar_hsa_circ_166295,RMVar_hsa_circ_166297 113607 RMVar_ID_113607 Human_SNP_ID_821721304 m1A Human chr14 - 99481481 99481481 99481481 GGGCGGCGCTGCCCTCAGTCGGTGGGTCACTCACCCCTCGCTTCAGGCAAGCCCCTCAGCGACGT GGGCGGCGCTGCCCTCAGTCGGTGGGTCACTCCCCCCTCGCTTCAGGCAAGCCCCTCAGCGACGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr14:99481454..99481570;chr14:99481453..99481556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113608 RMVar_ID_113608 Human_SNP_ID_821724043 m1A Human chr14 - 73718947 73718944 73718947 CGCATATGAAGAGCCACGCAGAGCAGGAGAAGAAGGCTGCAGCGCTGAGGCTGAAGGAGAAAGAG CGCATATGAAGAGCCACGCAGAGCAGGAGAAG___GCTGCAGCGCTGAGGCTGAAGGAGAAAGAG CCTT C MIDEAS Ensembl:ENSG00000156030 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:73718896..73719009 26863196 MeRIP-seq:(Medium) rs944178418 Functional Loss DEL ICGC 33..35 33 STAD 1 - Human_RBP_ID_451456,Human_RBP_ID_881020,Human_RBP_ID_4301363,Human_RBP_ID_26325937 Human_Splice_Rec_1534102 113609 RMVar_ID_113609 Human_SNP_ID_821727501 m1A Human chr14 - 24148074 24148074 24148074 GTGCTGCGAAAGACAGGGTTATTAAACTTGACACCACGCCAGTACCGAGGCCGCTGAGGGCTGAG GTGCTGCGAAAGACAGGGTTATTAAACTTGACGCCACGCCAGTACCGAGGCCGCTGAGGGCTGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24148024..24148113 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 113610 RMVar_ID_113610 Human_SNP_ID_821740905 m1A Human chr14 - 20458662 20458662 20458662 ATGGAAGCATGCACGGCGATATGGAGGCATCTATGCAGCCTGGGCATTTGTCATCCTGTTGGCTG ATGGAAGCATGCACGGCGATATGGAGGCATCTGTGCAGCCTGGGCATTTGTCATCCTGTTGGCTG T C PIP4P1 Ensembl:ENSG00000165782 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20458448..20458725 26863196 MeRIP-seq:(Medium) rs1249307306 Functional Loss SNV COSMIC 33..33 33 thyroid medullary_carcinoma 2 head and neck Human_RBP_ID_442750,Human_RBP_ID_1490446,Human_RBP_ID_5493313,Human_RBP_ID_18647212,Human_RBP_ID_25122901 Human_Splice_Rec_1488458,Human_Splice_Rec_1488464,Human_Splice_Rec_1488465,Human_Splice_Rec_1488480,Human_Splice_Rec_1488488,Human_Splice_Rec_1488492 113611 RMVar_ID_113611 Human_SNP_ID_821741361 m1A Human chr14 - 28768169 28768169 28768169 AGTAGAGGGAGCCGGCGCGGTCCATGAAGGTGAGGCCGGTGGAGGTGAGGCGCGCACCGCGCTTG AGTAGAGGGAGCCGGCGCGGTCCATGAAGGTGTGGCCGGTGGAGGTGAGGCGCGCACCGCGCTTG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:28768071..28768275 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach 113612 RMVar_ID_113612 Human_SNP_ID_821753058 m1A Human chr14 + 101964687 101964687 101964687 CTTCTCATCGCTCCTGGAAGGTCCCGAGCGCGACACCATGTCGGAGCCCGGGGGCGGCGGCGGCG CTTCTCATCGCTCCTGGAAGGTCCCGAGCGCGGCACCATGTCGGAGCCCGGGGGCGGCGGCGGCG A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:101964591..101964699 26863410 MeRIP-seq:(Medium) rs17511858 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_231346,Human_RBP_ID_4281183,Human_RBP_ID_8797985,Human_RBP_ID_9282287,Human_RBP_ID_9323872,Human_RBP_ID_17669232,Human_RBP_ID_18418297,Human_RBP_ID_22439447 Clinvar_Rec_217,Clinvar_Rec_218,Clinvar_Rec_219,Clinvar_Rec_220,Clinvar_Rec_221 RMVar_hsa_circ_121811,RMVar_hsa_circ_127992,RMVar_hsa_circ_169153,RMVar_hsa_circ_94226,RMVar_hsa_circ_117712,RMVar_hsa_circ_169155,RMVar_hsa_circ_169156,RMVar_hsa_circ_169154 113613 RMVar_ID_113613 Human_SNP_ID_821762308 m1A Human chr14 + 59484188 59484188 59484188 ATGTAGCGCCGCTTGGCCAGCAGGGTGGGCCCAGACACCTCCGGACACCCCGCCAGCACGATACG ATGTAGCGCCGCTTGGCCAGCAGGGTGGGCCCGGACACCTCCGGACACCCCGCCAGCACGATACG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:59484145..59484330 26863196 MeRIP-seq:(Medium) rs1338941786 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 113614 RMVar_ID_113614 Human_SNP_ID_821779565 m1A Human chr14 - 70339907 70339907 70339907 TGAGGACAAGGTCAGTTGAAGTCAAGGGAATGAGGTTAAAAGAAGGAGGATGGTTAAGGTCTGTA TGAGGACAAGGTCAGTTGAAGTCAAGGGAATGGGGTTAAAAGAAGGAGGATGGTTAAGGTCTGTA T C SYNJ2BP-COX16,COX16 Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:70339904..70339988 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_23633798 113615 RMVar_ID_113615 Human_SNP_ID_821787565 m1A Human chr14 + 73103331 73103331 73103331 GGAACGAGAAAGGGAAAGAGAACGTGAACGAGAAAAGGAGAAAGAACGGGAGCGGGAACGAGAAC GGAACGAGAAAGGGAAAGAGAACGTGAACGAGTAAAGGAGAAAGAACGGGAGCGGGAACGAGAAC A T RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:73103282..73103450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_4458,Human_RBP_ID_197250,Human_RBP_ID_231153,Human_RBP_ID_813043,Human_RBP_ID_9369167,Human_RBP_ID_12412202,Human_RBP_ID_17067520,Human_RBP_ID_18411097,Human_RBP_ID_22926360,Human_RBP_ID_23118239,Human_RBP_ID_23272482,Human_RBP_ID_23635261,Human_RBP_ID_24543698,Human_RBP_ID_25127688,Human_RBP_ID_26325207,Human_RBP_ID_27808404 RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_365770 113616 RMVar_ID_113616 Human_SNP_ID_821794527 m1A Human chr14 + 79845607 79845607 79845607 CGACCCAGAGAGACAGAGAGAGAGAGAGACAGAGAGAGAGACGGAGACGGGGAGAGAGACGGAGA CGACCCAGAGAGACAGAGAGAGAGAGAGACAGGGAGAGAGACGGAGACGGGGAGAGAGACGGAGA A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:79845527..79845758 26863196 MeRIP-seq:(Medium) rs568537368 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113617 RMVar_ID_113617 Human_SNP_ID_821833615 m1A Human chr14 + 96833516 96833516 96833516 AAAGCAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGAGACATCTTGCAGAACAATTTGCAGTTGG AAAGCAGCTCAAGCTGGAAGACAGAGCTCTGCGAAGAGACATCTTGCAGAACAATTTGCAGTTGG A G VRK1 Ensembl:ENSG00000100749 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2145635 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_17856051 Human_Splice_Rec_1551558,Human_Splice_Rec_1551582 Clinvar_Rec_216 GWAS_ID_7388,GWAS_ID_7389,GWAS_ID_7390,GWAS_ID_7391,GWAS_ID_7392,GWAS_ID_7393,GWAS_ID_7394,GWAS_ID_7395,GWAS_ID_7396,GWAS_ID_7397,GWAS_ID_7398,GWAS_ID_7399,GWAS_ID_7400,GWAS_ID_7401 RMVar_hsa_circ_116596,RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_309331,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_361287,RMVar_hsa_circ_168922,RMVar_hsa_circ_323937,RMVar_hsa_circ_271676,RMVar_hsa_circ_300344,RMVar_hsa_circ_269902,RMVar_hsa_circ_168926,RMVar_hsa_circ_168928,RMVar_hsa_circ_13272,RMVar_hsa_circ_168929,RMVar_hsa_circ_168927,RMVar_hsa_circ_168925 113618 RMVar_ID_113618 Human_SNP_ID_821845403 m1A Human chr14 + 63727644 63727644 63727644 GTTGCGGCGCAGAGCGCCCGCGCGCCGCGGCGAGGCCGGGCCCAGCTCGGCCGCCAGCCCGTTCC GTTGCGGCGCAGAGCGCCCGCGCGCCGCGGCGTGGCCGGGCCCAGCTCGGCCGCCAGCCCGTTCC A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:63727544..63727841 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - 113619 RMVar_ID_113619 Human_SNP_ID_821851121 m1A Human chr14 + 58351286 58351285 58351286 AGAAGAAAATTAAAAAACAGGAGGATTCTGACAAAGACTCAGATGAAGAGGAAGAGAAAAGCCAA AGAAGAAAATTAAAAAACAGGAGGATTCTGAC_AAGACTCAGATGAAGAGGAAGAGAAAAGCCAA CA C ARID4A Ensembl:ENSG00000032219 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:58351052..58351328 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUSC 1 - Human_RBP_ID_3944534,Human_RBP_ID_26325127 Human_Splice_Rec_1519109,Human_Splice_Rec_1519153,Human_Splice_Rec_1519199,Human_Splice_Rec_1519277,Human_Splice_Rec_1519301 Human_miRNA_ID_891344,Human_miRNA_ID_2404173,Human_miRNA_ID_2947659 RMVar_hsa_circ_21788,RMVar_hsa_circ_56121,RMVar_hsa_circ_29081,RMVar_hsa_circ_80483,RMVar_hsa_circ_166951,RMVar_hsa_circ_31589,RMVar_hsa_circ_166955,RMVar_hsa_circ_91708,RMVar_hsa_circ_344086,RMVar_hsa_circ_166957,RMVar_hsa_circ_268713,RMVar_hsa_circ_166958 113620 RMVar_ID_113620 Human_SNP_ID_821874259 m1A Human chr14 + 49586651 49586632 49586651 GGGAGGCTGAGGCTGGAGGATCGCTTGAGTCCAGGAGTTCTGGGCTGTAGTGCGCTATGCCGATC GGGAGGCTGAGGCT___________________GGAGTTCTGGGCTGTAGTGCGCTATGCCGATC TGGAGGATCGCTTGAGTCCA T RN7SL1 Ensembl:ENSG00000276168 Other exon GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr14:49586601..49586859;chr14:49586601..49586806 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 15..33 33 ESCA 1 - Human_RBP_ID_446267,Human_RBP_ID_3470192,Human_RBP_ID_5095641,Human_RBP_ID_9042120,Human_RBP_ID_18199507,Human_RBP_ID_18206936,Human_RBP_ID_23623623,Human_RBP_ID_27431320 Human_miRNA_ID_3179796,Human_miRNA_ID_3181746,Human_miRNA_ID_3181860,Human_miRNA_ID_3181973,Human_miRNA_ID_3182085,Human_miRNA_ID_3182199,Human_miRNA_ID_3182312,Human_miRNA_ID_3182631,Human_miRNA_ID_3182742,Human_miRNA_ID_3184519 113621 RMVar_ID_113621 Human_SNP_ID_821882056 m1A Human chr14 - 23307904 23307904 23307904 AGCGGGTCTCGAACTCATCTCCAGCTGCCCGCATGGCTTGGTGCAGCGGGTCAGCTGCTGGGCCC AGCGGGTCTCGAACTCATCTCCAGCTGCCCGCGTGGCTTGGTGCAGCGGGTCAGCTGCTGGGCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:23307858..23307942 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic 3 skin 113622 RMVar_ID_113622 Human_SNP_ID_821905776 m1A Human chr14 + 74818296 74818296 74818296 ATGATGCGTCTAGATATTCGTTCTTTGCTGCAAGATGCTGCTATTGAAGAGGTGAGTATCCTTTG ATGATGCGTCTAGATATTCGTTCTTTGCTGCAGGATGCTGCTATTGAAGAGGTGAGTATCCTTTG A G YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74818250..74821093 32194978 MeRIP-seq:(Medium) rs1180540945 Functional Loss SNV COSMIC 33..33 33 central_nervous_system ependymoma 2 brain Human_RBP_ID_39539,Human_RBP_ID_1824410,Human_RBP_ID_3461514,Human_RBP_ID_9369206,Human_RBP_ID_18979783,Human_RBP_ID_27808442 Human_Splice_Rec_1536234,Human_Splice_Rec_1536235,Human_Splice_Rec_1536270,Human_Splice_Rec_1536271,Human_Splice_Rec_1536304,Human_Splice_Rec_1536305,Human_Splice_Rec_1536330,Human_Splice_Rec_1536331,Human_Splice_Rec_1536334,Human_Splice_Rec_1536335,Human_Splice_Rec_1536339 Human_miRNA_ID_363787,Human_miRNA_ID_371002,Human_miRNA_ID_378175,Human_miRNA_ID_1238776,Human_miRNA_ID_1454539,Human_miRNA_ID_1937890,Human_miRNA_ID_1948990,Human_miRNA_ID_2101241,Human_miRNA_ID_2107195,Human_miRNA_ID_2113139,Human_miRNA_ID_2596933,Human_miRNA_ID_2650229,Human_miRNA_ID_2652179,Human_miRNA_ID_2739842,Human_miRNA_ID_3040440 RMVar_hsa_circ_8535,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_357377,RMVar_hsa_circ_72065,RMVar_hsa_circ_350698,RMVar_hsa_circ_318406,RMVar_hsa_circ_17700,RMVar_hsa_circ_167946,RMVar_hsa_circ_44316,RMVar_hsa_circ_44818,RMVar_hsa_circ_45930,RMVar_hsa_circ_266086,RMVar_hsa_circ_33547,RMVar_hsa_circ_17049,RMVar_hsa_circ_27138 113623 RMVar_ID_113623 Human_SNP_ID_821925233 m1A Human chr14 + 99510308 99510308 99510308 CCACCGCCGCTGCCACACCGGCCCCCGCCCCCACCCCCCTCCAGCTACATGACCGGGATGTCCAC CCACCGCCGCTGCCACACCGGCCCCCGCCCCCCCCCCCCTCCAGCTACATGACCGGGATGTCCAC A C CCNK Ensembl:ENSG00000090061 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:99510178..99510379 32194978 MeRIP-seq:(Medium) rs745936510 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_454603,Human_RBP_ID_17363393 Human_miRNA_ID_464312,Human_miRNA_ID_1559617 113624 RMVar_ID_113624 Human_SNP_ID_821942611 m1A Human chr14 + 102086377 102086377 102086377 TCGGTTGGTCTTGGGTCTGGGTTTCCTCAGGCATCTGGAACGACACCGCGCCGGTTTAAAACCTT TCGGTTGGTCTTGGGTCTGGGTTTCCTCAGGCTTCTGGAACGACACCGCGCCGGTTTAAAACCTT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated chr14:102086276..102086400;chr14:102086276..102086425;chr14:102086351..102086400 26863196,26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 113625 RMVar_ID_113625 Human_SNP_ID_821951705 m1A Human chr14 - 100561043 100561042 100561043 CATGTCAGGCCCGCATGGGGCTCCCCCTCCCCACCCCCCAACTACCACAGGCAGAAAATCCTTCC CATGTCAGGCCCGCATGGGGCTCCCCCTCCCC_CCCCCCAACTACCACAGGCAGAAAATCCTTCC GT G BEGAIN Ensembl:ENSG00000183092 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:100561033..100561226 26863196 MeRIP-seq:(Medium) rs1566973457 Functional Loss DEL ICGC 33..33 33 CHOL 1 - 113626 RMVar_ID_113626 Human_SNP_ID_821973569 m1A Human chr14 + 22876163 22876163 22876163 CGCTGTCGGCATTGCCAGCCTGGCAATTTCCGATGCCGGGACGAGAAGTGCGTGTATGAGACGTG CGCTGTCGGCATTGCCAGCCTGGCAATTTCCGGTGCCGGGACGAGAAGTGCGTGTATGAGACGTG A G LRP10 Ensembl:ENSG00000197324 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:22876120..22876195 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8797788,Human_RBP_ID_23616062 RMVar_hsa_circ_98648,RMVar_hsa_circ_165236,RMVar_hsa_circ_115767,RMVar_hsa_circ_165238,RMVar_hsa_circ_94006,RMVar_hsa_circ_165239 113627 RMVar_ID_113627 Human_SNP_ID_821975605 m1A Human chr14 - 22589172 22589172 22589172 GTCCTCCAAGAGTTTGGGGCGCGGACCGGAGTACCTTGCGTGCAGTTATGTCGGCGTCGGTAGTG GTCCTCCAAGAGTTTGGGGCGCGGACCGGAGTGCCTTGCGTGCAGTTATGTCGGCGTCGGTAGTG T C DAD1 Ensembl:ENSG00000129562 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:22588989..22589225;chr14:22589126..22589200;chr14:22589010..22589225;chr14:22589061..22589225;chr14:22589071..22589225 26863196 MeRIP-seq:(Medium) rs139670797 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_39808,Human_RBP_ID_230825,Human_RBP_ID_443350,Human_RBP_ID_1491316,Human_RBP_ID_4287670,Human_RBP_ID_5141049,Human_RBP_ID_5418035,Human_RBP_ID_5463236,Human_RBP_ID_9040094,Human_RBP_ID_9324009,Human_RBP_ID_12298771,Human_RBP_ID_23615986,Human_RBP_ID_26427901,Human_RBP_ID_27430426 113628 RMVar_ID_113628 Human_SNP_ID_821976186 m1A Human chr14 - 102933111 102933111 102933111 CAGGACCAGTGACACCCTGCGTCCCTGTGTGCATTAAGTTCATTCTGGGTCGCAGCCATGAAGTG CAGGACCAGTGACACCCTGCGTCCCTGTGTGCGTTAAGTTCATTCTGGGTCGCAGCCATGAAGTG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4708 Functional Loss SNV ICGC 33..33 33 LUSC 3 - Human_RBP_ID_26920484,Human_RBP_ID_27224015 Human_miRNA_ID_359331,Human_miRNA_ID_1475318,Human_miRNA_ID_1480278,Human_miRNA_ID_2888625,Human_miRNA_ID_2888972 GWAS_ID_7426,GWAS_ID_7427,GWAS_ID_7428,GWAS_ID_7429,GWAS_ID_7430,GWAS_ID_7431 RMVar_hsa_circ_110689,RMVar_hsa_circ_125390,RMVar_hsa_circ_80151,RMVar_hsa_circ_93325,RMVar_hsa_circ_108427,RMVar_hsa_circ_89707,RMVar_hsa_circ_169451,RMVar_hsa_circ_169453,RMVar_hsa_circ_169454,RMVar_hsa_circ_169455,RMVar_hsa_circ_169452,RMVar_hsa_circ_169450 113629 RMVar_ID_113629 Human_SNP_ID_822002968 m1A Human chr14 - 65102392 65102392 65102392 TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTCACCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC TTGTTGTTGTCGGTGACTTCCCCCTCCCCTTCCCCCCTTCCCCTCCCCGCCGCCGCTGCAGTGGC T G MAX Ensembl:ENSG00000125952 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:65102326..65102475 32194978 MeRIP-seq:(Medium) rs1005278567 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_196866,Human_RBP_ID_449893,Human_RBP_ID_4313744,Human_RBP_ID_5418228,Human_RBP_ID_5439483,Human_RBP_ID_5463488,Human_RBP_ID_5494151,Human_RBP_ID_5645796,Human_RBP_ID_8181731,Human_RBP_ID_18936814,Human_RBP_ID_23208730,Human_RBP_ID_23631322,Human_RBP_ID_27808376 Human_Splice_Rec_1526539,Human_Splice_Rec_1526545,Human_Splice_Rec_1526553,Human_Splice_Rec_1526559,Human_Splice_Rec_1526569,Human_Splice_Rec_1526577,Human_Splice_Rec_1526585,Human_Splice_Rec_1526587,Human_Splice_Rec_1526593,Human_Splice_Rec_1526599,Human_Splice_Rec_1526627,Human_Splice_Rec_1526635,Human_Splice_Rec_1526641,Human_Splice_Rec_1526649,Human_Splice_Rec_1526653,Human_Splice_Rec_1526659,Human_Splice_Rec_1526663 113630 RMVar_ID_113630 Human_SNP_ID_822009609 m1A Human chr14 + 69611696 69611696 69611696 TCCTCCCTCCCTCCCGCCCGCTTCCTCTGCCCACAGCGCCGGCCAGAGCGAGCTAGACAAGGGCA TCCTCCCTCCCTCCCGCCCGCTTCCTCTGCCCGCAGCGCCGGCCAGAGCGAGCTAGACAAGGGCA A G SUSD6 Ensembl:ENSG00000100647 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:69611655..69611763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 113631 RMVar_ID_113631 Human_SNP_ID_822010352 m1A Human chr14 + 66508209 66508209 66508209 CTTGGGTCTCGCGCTCCGCAGAGCGTTCCGACACTCTCCGGCCTCGTTCTGCCGCCTCCGCGCGC CTTGGGTCTCGCGCTCCGCAGAGCGTTCCGACGCTCTCCGGCCTCGTTCTGCCGCCTCCGCGCGC A G GPHN Ensembl:ENSG00000171723 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:66508158..66508353 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_1275904 113632 RMVar_ID_113632 Human_SNP_ID_822035792 m1A Human chr14 - 102368782 102368782 102368782 TGCCACAGTACAAGCTATCATATCCCTCGCCTACACTGCTGCCATGGTCTTCCACACCTGCCCCC TGCCACAGTACAAGCTATCATATCCCTCGCCTTCACTGCTGCCATGGTCTTCCACACCTGCCCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:102368772..102368935 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113633 RMVar_ID_113633 Human_SNP_ID_822066552 m1A Human chr14 + 73105951 73105951 73105951 AGAGCGAGAACGAGAACGGGAGCGAGAGAGAGAGCGAGAGAGGGAACGGGAGCGAGAAAGAGAAA AGAGCGAGAACGAGAACGGGAGCGAGAGAGAGCGCGAGAGAGGGAACGGGAGCGAGAAAGAGAAA A C RBM25 Ensembl:ENSG00000119707 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:73105792..73106025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BLCA 1 - Human_RBP_ID_39586,Human_RBP_ID_197096,Human_RBP_ID_231154,Human_RBP_ID_813044,Human_RBP_ID_1502466,Human_RBP_ID_4314133,Human_RBP_ID_9345016,Human_RBP_ID_17067523,Human_RBP_ID_22925066,Human_RBP_ID_23113672,Human_RBP_ID_23272483,Human_RBP_ID_24543701,Human_RBP_ID_25127691,Human_RBP_ID_26325210 Human_Splice_Rec_1532558,Human_Splice_Rec_1532608,Human_Splice_Rec_1532642,Human_Splice_Rec_1532718 RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_68396,RMVar_hsa_circ_51672,RMVar_hsa_circ_55992,RMVar_hsa_circ_365770 113634 RMVar_ID_113634 Human_SNP_ID_822076849 m1A Human chr14 + 74502762 74502762 74502762 GAGTGACCGGCTGTGTTGGGGAAGGCAGGCTCAGGGACGGTGTCCTCGGGGCCCAGGTAGTTGTA GAGTGACCGGCTGTGTTGGGGAAGGCAGGCTCGGGGACGGTGTCCTCGGGGCCCAGGTAGTTGTA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74502711..74503578 32194978 MeRIP-seq:(Medium) rs561011462 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 113635 RMVar_ID_113635 Human_SNP_ID_822089886 m1A Human chr14 - 104939830 104939830 104939830 ATGCCCAGCCTTAGGCGCTCTTTCAGGGACAGAGGCGGGGCTGGAAAGCTGGAAGTGGCTCAGAC ATGCCCAGCCTTAGGCGCTCTTTCAGGGACAGGGGCGGGGCTGGAAAGCTGGAAGTGGCTCAGAC T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104939780..104939981 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_118063,RMVar_hsa_circ_122947,RMVar_hsa_circ_169673,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 113636 RMVar_ID_113636 Human_SNP_ID_822099053 m1A Human chr14 + 92709751 92709751 92709751 GATCATTGGTGTTCATCAGTTTCCTTTTCATGATGGTGAGAGGCACATCAGGGCTGGGGGTGAGG GATCATTGGTGTTCATCAGTTTCCTTTTCATGGTGGTGAGAGGCACATCAGGGCTGGGGGTGAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:92709726..92709750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine 113637 RMVar_ID_113637 Human_SNP_ID_822151682 m1A Human chr14 - 34764788 34764788 34764788 TATGGGAGGTGAGGATGATGAAGTTGATGGCGATGAAGAAGAAGGTCAAAGTGAGGAGGAAGAGT TATGGGAGGTGAGGATGATGAAGTTGATGGCGGTGAAGAAGAAGGTCAAAGTGAGGAGGAAGAGT T C BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr14:34764693..34764954 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_813831,Human_RBP_ID_2411926,Human_RBP_ID_4292622,Human_RBP_ID_5522677,Human_RBP_ID_6342602,Human_RBP_ID_22737481,Human_RBP_ID_22926462,Human_RBP_ID_24543821,Human_RBP_ID_26325740 Human_Splice_Rec_1506395,Human_Splice_Rec_1506443,Human_Splice_Rec_1506491 RMVar_hsa_circ_116030,RMVar_hsa_circ_88530,RMVar_hsa_circ_165883,RMVar_hsa_circ_338990,RMVar_hsa_circ_366461,RMVar_hsa_circ_271486,RMVar_hsa_circ_60874,RMVar_hsa_circ_83760,RMVar_hsa_circ_99897,RMVar_hsa_circ_165889,RMVar_hsa_circ_165890,RMVar_hsa_circ_165888,RMVar_hsa_circ_165892,RMVar_hsa_circ_365684,RMVar_hsa_circ_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,RMVar_hsa_circ_165893 113638 RMVar_ID_113638 Human_SNP_ID_822152961 m1A Human chr14 - 24811050 24811050 24811050 AAATTTAATAAACTGTATAAGTTAACTATAATATTTTATACTTTCTTTTTGGTGTCTTAAAAATT AAATTTAATAAACTGTATAAGTTAACTATAATGTTTTATACTTTCTTTTTGGTGTCTTAAAAATT T C STXBP6 Ensembl:ENSG00000168952 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3825590 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_26623578 113639 RMVar_ID_113639 Human_SNP_ID_822159488 m1A Human chr14 - 69055218 69055218 69055218 ACGCCTTCCACCTGGGGCCCCTGCGGGTCACCACCACAAACACAGTAGCCTCAACTCCACCAACA ACGCCTTCCACCTGGGGCCCCTGCGGGTCACCGCCACAAACACAGTAGCCTCAACTCCACCAACA T C DCAF5 Ensembl:ENSG00000139990 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:69055167..69055323 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 8 lung Human_RBP_ID_27433839 RMVar_hsa_circ_89321,RMVar_hsa_circ_167494 113640 RMVar_ID_113640 Human_SNP_ID_822161511 m1A Human chr14 + 23275543 23275543 23275543 GTTTAAACAGTTACTAAGTTGGTTCATCTTTCAGTAACAGACCTCCCCTCCCCCAGCTCCCCACT GTTTAAACAGTTACTAAGTTGGTTCATCTTTCCGTAACAGACCTCCCCTCCCCCAGCTCCCCACT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23275493..23275881 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113641 RMVar_ID_113641 Human_SNP_ID_822163903 m1A Human chr14 + 74084393 74084393 74084393 CTCGCACTGCCGCCGCCGCCAATAGCGCCGCCATGGCTCTCGGCCGCCCTAGCTCCGCACCCCGC CTCGCACTGCCGCCGCCGCCAATAGCGCCGCCTTGGCTCTCGGCCGCCCTAGCTCCGCACCCCGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr14:74084238..74084403;chr14:74084240..74084413;chr14:74084257..74084416;chr14:74084288..74084397 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 113642 RMVar_ID_113642 Human_SNP_ID_822165177 m1A Human chr14 - 104714179 104714164 104714179 TGGTGGCCACTGGATGGAGGGACACACCAGTGAAGGGCAGGCACCCTGCCCCCGAGCCAGCCCAG TGGTGGCCACTGGATGGAGGGACACACCAGTG_______________GCCCCCGAGCCAGCCCAG CAGGGTGCCTGCCCTT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104714176..104714778 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..47 33 LICA 1 - 113643 RMVar_ID_113643 Human_SNP_ID_822172446 m1A Human chr14 + 74763990 74763990 74763990 TATATGCCCCCATCTCAGTCTTACATGCCCCCACCTCAGCCGCCACCCTCTTACTACCCCCCGAC TATATGCCCCCATCTCAGTCTTACATGCCCCCCCCTCAGCCGCCACCCTCTTACTACCCCCCGAC A C YLPM1 Ensembl:ENSG00000119596 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:74763896..74764105 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_9323815,Human_RBP_ID_17076481,Human_RBP_ID_18936890,Human_RBP_ID_22045301,Human_RBP_ID_22188625,Human_RBP_ID_22925166 113644 RMVar_ID_113644 Human_SNP_ID_822185852 m1A Human chr14 + 105248990 105248990 105248990 GGGCCGCGCAGCCCGCCCAGCGCCCCCGCGCCAGCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC GGGCCGCGCAGCCCGCCCAGCGCCCCCGCGCCCGCGCCGCCGCCGCCCGCGCCCGCGCCGCCCAC A C BTBD6 Ensembl:ENSG00000184887 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:105248635..105249139 26863410 MeRIP-seq:(Medium) rs2816604 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 20 head and neck Human_RBP_ID_231316 Human_Splice_Rec_1561759,Human_Splice_Rec_1561767,Human_Splice_Rec_1561773,Human_Splice_Rec_1561783 RMVar_hsa_circ_114110,RMVar_hsa_circ_94676,RMVar_hsa_circ_169705,RMVar_hsa_circ_169706 113645 RMVar_ID_113645 Human_SNP_ID_822195584 m1A Human chr14 + 96833520 96833520 96833520 CAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGAGACATCTTGCAGAACAATTTGCAGTTGGAGAG CAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGTGACATCTTGCAGAACAATTTGCAGTTGGAGAG A T VRK1 Ensembl:ENSG00000100749 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:96797403..96833572 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1502064,Human_RBP_ID_17856051 Human_Splice_Rec_1551558,Human_Splice_Rec_1551582 RMVar_hsa_circ_116596,RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_309331,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_361287,RMVar_hsa_circ_168922,RMVar_hsa_circ_323937,RMVar_hsa_circ_271676,RMVar_hsa_circ_300344,RMVar_hsa_circ_269902,RMVar_hsa_circ_168926,RMVar_hsa_circ_168928,RMVar_hsa_circ_13272,RMVar_hsa_circ_168929,RMVar_hsa_circ_168927,RMVar_hsa_circ_168925 113646 RMVar_ID_113646 Human_SNP_ID_822195609 m1A Human chr14 + 96833520 96833520 96833520 CAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGAGACATCTTGCAGAACAATTTGCAGTTGGAGAG CAGCTCAAGCTGGAAGACAGAGCTCTGCAAAGGGACATCTTGCAGAACAATTTGCAGTTGGAGAG A G VRK1 Ensembl:ENSG00000100749 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:96797403..96833572 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_1502064,Human_RBP_ID_17856051 Human_Splice_Rec_1551558,Human_Splice_Rec_1551582 RMVar_hsa_circ_116596,RMVar_hsa_circ_89649,RMVar_hsa_circ_112010,RMVar_hsa_circ_106609,RMVar_hsa_circ_309331,RMVar_hsa_circ_168923,RMVar_hsa_circ_168924,RMVar_hsa_circ_361287,RMVar_hsa_circ_168922,RMVar_hsa_circ_323937,RMVar_hsa_circ_271676,RMVar_hsa_circ_300344,RMVar_hsa_circ_269902,RMVar_hsa_circ_168926,RMVar_hsa_circ_168928,RMVar_hsa_circ_13272,RMVar_hsa_circ_168929,RMVar_hsa_circ_168927,RMVar_hsa_circ_168925 113647 RMVar_ID_113647 Human_SNP_ID_822195727 m1A Human chr14 - 104889760 104889760 104889760 CACCCAGTGGATTTACTCTGAATGGGCTACTCACCTGGCAATCTCCGCAATCTCTGCCGTCTGCA CACCCAGTGGATTTACTCTGAATGGGCTACTCCCCTGGCAATCTCCGCAATCTCTGCCGTCTGCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104889753..104889837 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney 113648 RMVar_ID_113648 Human_SNP_ID_822209143 m1A Human chr14 - 50757155 50757155 50757155 AGAACTCACTGCAGAGGTTTTCAGGTTGCAGGATGAGCTGAAGAAAATGGAGGAAGTCACTGAAA AGAACTCACTGCAGAGGTTTTCAGGTTGCAGGGTGAGCTGAAGAAAATGGAGGAAGTCACTGAAA T C NIN Ensembl:ENSG00000100503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50757106..50757256 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine RMVar_hsa_circ_46869,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_324799,RMVar_hsa_circ_64625,RMVar_hsa_circ_166564,RMVar_hsa_circ_23643,RMVar_hsa_circ_23989,RMVar_hsa_circ_298344,RMVar_hsa_circ_57623,RMVar_hsa_circ_72339,RMVar_hsa_circ_266035,RMVar_hsa_circ_359044,RMVar_hsa_circ_13706 113649 RMVar_ID_113649 Human_SNP_ID_822239075 m1A Human chr14 + 50822055 50822055 50822055 GGGCCTCATGCTGGTCCTGCTCCACCTCATCCATCCCATAGCCCACAGTGCTCACCTGTGTGTAA GGGCCTCATGCTGGTCCTGCTCCACCTCATCCGTCCCATAGCCCACAGTGCTCACCTGTGTGTAA A G AL133485.2 Ensembl:ENSG00000258843 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:50821970..50822141 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 113650 RMVar_ID_113650 Human_SNP_ID_822246577 m1A Human chr14 + 24151351 24151351 24151351 GGATCGTCATGGCAACCTTGATGAAGCTGTGGAGGAGTGTGTGAGGACCAGGCGAAGGAAGGTAT GGATCGTCATGGCAACCTTGATGAAGCTGTGGTGGAGTGTGTGAGGACCAGGCGAAGGAAGGTAT A T RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:24151260..24151400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_813732,Human_RBP_ID_880493,Human_RBP_ID_5522631,Human_RBP_ID_9368631,Human_RBP_ID_18979369,Human_RBP_ID_26324643 Human_Splice_Rec_1498477,Human_Splice_Rec_1498517,Human_Splice_Rec_1498586,Human_Splice_Rec_1498587,Human_Splice_Rec_1498621,Human_Splice_Rec_1498645,Human_Splice_Rec_1498733 Human_miRNA_ID_2450647,Human_miRNA_ID_2540093,Human_miRNA_ID_2708806 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 113651 RMVar_ID_113651 Human_SNP_ID_822262778 m1A Human chr14 - 95446042 95446042 95446042 CTCCCGCCTGAAAGAGCTGCTGACGATGCTGCAGCTGAAGAAAGACCTCCTGATTGGCATCTTTG CTCCCGCCTGAAAGAGCTGCTGACGATGCTGCGGCTGAAGAAAGACCTCCTGATTGGCATCTTTG T C SYNE3 Ensembl:ENSG00000176438 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:95445991..95446150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_1550368,Human_Splice_Rec_1550400,Human_Splice_Rec_1550424,Human_Splice_Rec_1550452,Human_Splice_Rec_1550476 RMVar_hsa_circ_1241,RMVar_hsa_circ_3108,RMVar_hsa_circ_19012,RMVar_hsa_circ_23334,RMVar_hsa_circ_47378,RMVar_hsa_circ_7318 113652 RMVar_ID_113652 Human_SNP_ID_822303180 m1A Human chr14 - 104175996 104175996 104175996 ATTGATGCTGCTGATGATGCTGACTGGCCGGGACCCCGAGGCCAGGGCCCGCAGGGAGCAGTCAC ATTGATGCTGCTGATGATGCTGACTGGCCGGGTCCCCGAGGCCAGGGCCCGCAGGGAGCAGTCAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104175950..104176058 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113653 RMVar_ID_113653 Human_SNP_ID_822303217 m1A Human chr14 - 74799466 74799466 74799466 ACCGTTCTCTTTCCCAGTCCATTCTGTCAGGAACATAATCTCGCTTTTCCCGCCATGTATCTCCT ACCGTTCTCTTTCCCAGTCCATTCTGTCAGGAGCATAATCTCGCTTTTCCCGCCATGTATCTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:74799416..74799666 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver 113654 RMVar_ID_113654 Human_SNP_ID_822307647 m1A Human chr14 - 75279962 75279962 75279962 GGGCCACGGAGGAGACGAGGGCGGGCTGCACCAGCCACTGCAGGTCCGGACTGGTCGAGATGGCA GGGCCACGGAGGAGACGAGGGCGGGCTGCACCGGCCACTGCAGGTCCGGACTGGTCGAGATGGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:75279399..75280200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung 113655 RMVar_ID_113655 Human_SNP_ID_822325050 m1A Human chr14 + 20343686 20343686 20343686 CGGCGACGGAGCACCGGCGGCGGCAGGGCGAGAGGTTCGGAGCTCAATATCGCGGGACGGCATGC CGGCGACGGAGCACCGGCGGCGGCAGGGCGAGGGGTTCGGAGCTCAATATCGCGGGACGGCATGC A G PARP2 Ensembl:ENSG00000129484 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA Glucose starvation 4h chr14:20343626..20343738;chr14:20343626..20343749 26863410,26863196 MeRIP-seq:(Medium) rs776404988 Functional Loss SNV COSMIC 33..33 33 cervix small_cell_carcinoma 3 uterus Human_RBP_ID_231716 Human_Splice_Rec_1487575,Human_Splice_Rec_1487605,Human_Splice_Rec_1487635,Human_Splice_Rec_1487647 RMVar_hsa_circ_165080 113656 RMVar_ID_113656 Human_SNP_ID_822333022 m1A Human chr14 - 24432289 24432286 24432289 GAGAGGCATTCCCATTGTGGAGCCGCTGGAGGAGGGAGGCTCCTCGGGACTGAGCTGCCCTGTGA GAGAGGCATTCCCATTGTGGAGCCGCTGGAGG___GAGGCTCCTCGGGACTGAGCTGCCCTGTGA CCCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:24432239..24432389 32194978 MeRIP-seq:(Medium) rs1289978638 Functional Loss DEL ICGC 33..35 33 LICA 1 - 113657 RMVar_ID_113657 Human_SNP_ID_822346228 m1A Human chr14 - 77751446 77751446 77751446 TTTTGGAGATGGAGGTGCTTTTCCAGAGATCCATGTGGCCCAGTATCCACTGGATATGGGACGAA TTTTGGAGATGGAGGTGCTTTTCCAGAGATCCGTGTGGCCCAGTATCCACTGGATATGGGACGAA T C SNW1 Ensembl:ENSG00000100603 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr14:77751426..77751450 26863196 MeRIP-seq:(Medium) rs1344578188 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4303817,Human_RBP_ID_6388318,Human_RBP_ID_17856470,Human_RBP_ID_22439663,Human_RBP_ID_23638348 Human_Splice_Rec_1539736,Human_Splice_Rec_1539782,Human_Splice_Rec_1539808,Human_Splice_Rec_1539840,Human_Splice_Rec_1539850 Human_miRNA_ID_311276,Human_miRNA_ID_1157260,Human_miRNA_ID_1336129,Human_miRNA_ID_1563260,Human_miRNA_ID_2506609,Human_miRNA_ID_3043180 RMVar_hsa_circ_32238,RMVar_hsa_circ_94961,RMVar_hsa_circ_82103,RMVar_hsa_circ_168227,RMVar_hsa_circ_74560,RMVar_hsa_circ_168228 113658 RMVar_ID_113658 Human_SNP_ID_822354524 m1A Human chr14 + 20457233 20457233 20457233 AAATTGACCTTCGCAACCCCAAGGGGAACAAAAAGAATGCTGGCTTCACGCCACAAGAGCGCCAA AAATTGACCTTCGCAACCCCAAGGGGAACAAATAGAATGCTGGCTTCACGCCACAAGAGCGCCAA A T APEX1 Ensembl:ENSG00000100823 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20457183..20457335 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_442708,Human_RBP_ID_997769,Human_RBP_ID_18647198 113659 RMVar_ID_113659 Human_SNP_ID_822354550 m1A Human chr14 + 20457233 20457233 20457233 AAATTGACCTTCGCAACCCCAAGGGGAACAAAAAGAATGCTGGCTTCACGCCACAAGAGCGCCAA AAATTGACCTTCGCAACCCCAAGGGGAACAAACAGAATGCTGGCTTCACGCCACAAGAGCGCCAA A C APEX1 Ensembl:ENSG00000100823 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:20457183..20457335 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_442708,Human_RBP_ID_997769,Human_RBP_ID_18647198 113660 RMVar_ID_113660 Human_SNP_ID_822382292 m1A Human chr14 + 90292756 90292756 90292756 CTCGGTTTGCTTCTTGGTCTTATCAGGGCGCCAGGGCCGCCAGTGCCTCTGGTCACGGGAACGCT CTCGGTTTGCTTCTTGGTCTTATCAGGGCGCCGGGGCCGCCAGTGCCTCTGGTCACGGGAACGCT A G AL161662.1 Ensembl:ENSG00000287437 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:90292710..90292808 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113661 RMVar_ID_113661 Human_SNP_ID_822389209 m1A Human chr14 + 73874094 73874094 73874094 ACACCTTGGCAGCTATCTCAAGTCGTTGATGGAGGAGGTATTGGAATTATAGAAGAAAGCAAACA ACACCTTGGCAGCTATCTCAAGTCGTTGATGGTGGAGGTATTGGAATTATAGAAGAAAGCAAACA A T PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11159042 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_3945015,Human_RBP_ID_23635788,Human_RBP_ID_26325232 Human_Splice_Rec_1534178,Human_Splice_Rec_1534196,Human_Splice_Rec_1534214,Human_Splice_Rec_1534228,Human_Splice_Rec_1534244,Human_Splice_Rec_1534254,Human_Splice_Rec_1534268 Human_miRNA_ID_2418543,Human_miRNA_ID_3092017 GWAS_ID_8783,GWAS_ID_8784,GWAS_ID_8785,GWAS_ID_8786,GWAS_ID_8787,GWAS_ID_8788,GWAS_ID_8789,GWAS_ID_8790,GWAS_ID_8791,GWAS_ID_8792,GWAS_ID_8793,GWAS_ID_8794,GWAS_ID_8795,GWAS_ID_8796,GWAS_ID_8797,GWAS_ID_8798,GWAS_ID_8799,GWAS_ID_8800,GWAS_ID_8801,GWAS_ID_8802,GWAS_ID_8803,GWAS_ID_8804,GWAS_ID_8805,GWAS_ID_8806,GWAS_ID_8807,GWAS_ID_8808,GWAS_ID_8809,GWAS_ID_8810,GWAS_ID_8811,GWAS_ID_8812,GWAS_ID_8813,GWAS_ID_8814,GWAS_ID_8815,GWAS_ID_8816,GWAS_ID_8817,GWAS_ID_8818,GWAS_ID_8819,GWAS_ID_8820,GWAS_ID_8821,GWAS_ID_8822,GWAS_ID_8823,GWAS_ID_8824,GWAS_ID_8825,GWAS_ID_8826,GWAS_ID_8827,GWAS_ID_8828,GWAS_ID_8829,GWAS_ID_8830,GWAS_ID_8831,GWAS_ID_8832,GWAS_ID_8833,GWAS_ID_8834,GWAS_ID_8835 RMVar_hsa_circ_40215,RMVar_hsa_circ_305319,RMVar_hsa_circ_349232,RMVar_hsa_circ_355280,RMVar_hsa_circ_67974,RMVar_hsa_circ_65339,RMVar_hsa_circ_82128,RMVar_hsa_circ_101082,RMVar_hsa_circ_167807,RMVar_hsa_circ_167808,RMVar_hsa_circ_167806,RMVar_hsa_circ_359577,RMVar_hsa_circ_84235,RMVar_hsa_circ_57260,RMVar_hsa_circ_167811,RMVar_hsa_circ_61290,RMVar_hsa_circ_167812,RMVar_hsa_circ_353654,RMVar_hsa_circ_167810,RMVar_hsa_circ_365109,RMVar_hsa_circ_350552 113662 RMVar_ID_113662 Human_SNP_ID_822412999 m1A Human chr14 + 103703228 103703205 103703228 AGATCTGGCTGCCAAATCGGAGCTTCTGAAGCAGCTCTCCTGGAACGTCAGTGCGCAGCCGCGGC AGATCTGGCT_______________________GCTCTCCTGGAACGTCAGTGCGCAGCCGCGGC TGCCAAATCGGAGCTTCTGAAGCA T KLC1 Ensembl:ENSG00000126214 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:103703177..103703377 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 11..33 33 BRCA 1 - Human_RBP_ID_3442890 RMVar_hsa_circ_169599 113663 RMVar_ID_113663 Human_SNP_ID_822427629 m1A Human chr14 - 23059337 23059337 23059337 CGGGAACGGAACCGACAGCTGGAGCGAGAGAAACGTCGGGAGCACAGTCGGGAGAGGGACAGGGA CGGGAACGGAACCGACAGCTGGAGCGAGAGAACCGTCGGGAGCACAGTCGGGAGAGGGACAGGGA T G ACIN1 Ensembl:ENSG00000100813 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:23058844..23061525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - Human_RBP_ID_40708,Human_RBP_ID_5177001,Human_RBP_ID_5522605,Human_RBP_ID_5563077,Human_RBP_ID_6333978,Human_RBP_ID_8230388,Human_RBP_ID_12300119,Human_RBP_ID_22044444,Human_RBP_ID_22926208,Human_RBP_ID_23113651,Human_RBP_ID_23118217,Human_RBP_ID_23616376,Human_RBP_ID_24543642,Human_RBP_ID_26324882,Human_RBP_ID_26922654 113664 RMVar_ID_113664 Human_SNP_ID_822466053 m1A Human chr14 + 77616552 77616552 77616552 CACGCAGCCATTCGCCCGCACCGTGCGGCGGCAGCAGCAGCCTCCGGGCTCCGGCCGCATCTTCC CACGCAGCCATTCGCCCGCACCGTGCGGCGGCGGCAGCAGCCTCCGGGCTCCGGCCGCATCTTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:77616501..77616711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113665 RMVar_ID_113665 Human_SNP_ID_822474458 m1A Human chr14 + 55612404 55612404 55612404 AAGTAGTGTTAGGGAAAGAAAAAAGAAGGAAAAGAAACAAAAGCCTGTGCTTGAAGAGCAGGTCA AAGTAGTGTTAGGGAAAGAAAAAAGAAGGAAACGAAACAAAAGCCTGTGCTTGAAGAGCAGGTCA A C KTN1 Ensembl:ENSG00000126777 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:55612353..55612503 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 8 caecum,large intestine Human_RBP_ID_120173,Human_RBP_ID_1820765,Human_RBP_ID_17187308 Human_miRNA_ID_834479,Human_miRNA_ID_2359982 RMVar_hsa_circ_16694,RMVar_hsa_circ_266361,RMVar_hsa_circ_269272,RMVar_hsa_circ_53501,RMVar_hsa_circ_276588,RMVar_hsa_circ_336962,RMVar_hsa_circ_359358,RMVar_hsa_circ_334204,RMVar_hsa_circ_72947,RMVar_hsa_circ_45494,RMVar_hsa_circ_166840,RMVar_hsa_circ_166842,RMVar_hsa_circ_5842,RMVar_hsa_circ_166843,RMVar_hsa_circ_166841 113666 RMVar_ID_113666 Human_SNP_ID_822497739 m1A Human chr14 + 105438719 105438719 105438719 AGAACTCCTCCAGCAACCCATACCTGATCCGGAGAATCGAGGAGCTCAACAAGGTACTGGGGGGC AGAACTCCTCCAGCAACCCATACCTGATCCGGGGAATCGAGGAGCTCAACAAGGTACTGGGGGGC A G MTA1,TEX22 Ensembl:ENSG00000182979,Ensembl:ENSG00000226174 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105438651..105438750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1171291,Human_RBP_ID_1489905,Human_RBP_ID_1815809,Human_RBP_ID_3443379,Human_RBP_ID_3944749,Human_RBP_ID_4310666,Human_RBP_ID_6329550,Human_RBP_ID_8400877,Human_RBP_ID_12288812,Human_RBP_ID_17246682,Human_RBP_ID_18646898,Human_RBP_ID_18981180 Human_Splice_Rec_1562082,Human_Splice_Rec_1562083,Human_Splice_Rec_1562104,Human_Splice_Rec_1562105,Human_Splice_Rec_1562146,Human_Splice_Rec_1562147,Human_Splice_Rec_1562186,Human_Splice_Rec_1562187,Human_Splice_Rec_1562224,Human_Splice_Rec_1562225,Human_Splice_Rec_1562262,Human_Splice_Rec_1562263,Human_Splice_Rec_1562302,Human_Splice_Rec_1562303,Human_Splice_Rec_1562311,Human_Splice_Rec_1562325 RMVar_hsa_circ_14003,RMVar_hsa_circ_333657,RMVar_hsa_circ_373421,RMVar_hsa_circ_315519,RMVar_hsa_circ_327477,RMVar_hsa_circ_39157,RMVar_hsa_circ_169728,RMVar_hsa_circ_169729 113667 RMVar_ID_113667 Human_SNP_ID_822498052 m1A Human chr14 - 88563171 88563171 88563171 CTGGCTTCCCACCCCCGACCGGCACGGGCCTCACCCGGATCTTGCGGCTGATCTCGGTGCCGATC CTGGCTTCCCACCCCCGACCGGCACGGGCCTCGCCCGGATCTTGCGGCTGATCTCGGTGCCGATC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:88563151..88563175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 113668 RMVar_ID_113668 Human_SNP_ID_822562120 m1A Human chr14 - 20474753 20474753 20474753 CTGGGAATGTCACCTTCGAAGCAAACAATCCGAAAAAAATTTACAAAATTTCATTAATTCAGCTA CTGGGAATGTCACCTTCGAAGCAAACAATCCGGAAAAAATTTACAAAATTTCATTAATTCAGCTA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:20474751..20474966 32194978 MeRIP-seq:(Medium) rs763807017 Functional Loss SNV ICGC 33..33 33 STAD 1 - 113669 RMVar_ID_113669 Human_SNP_ID_822613966 m1A Human chr14 + 64727665 64727665 64727665 TGCCTGTGTCCACCTCCCTCCACCAGGATGGCAGCCAGGAGCGGCCGGTGAGCCTGACCTCTACC TGCCTGTGTCCACCTCCCTCCACCAGGATGGCGGCCAGGAGCGGCCGGTGAGCCTGACCTCTACC A G PLEKHG3 Ensembl:ENSG00000126822 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:64727616..64727767 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 6 lung Human_RBP_ID_880973,Human_RBP_ID_5463796 Human_Splice_Rec_1525846,Human_Splice_Rec_1525854,Human_Splice_Rec_1525886,Human_Splice_Rec_1525912,Human_Splice_Rec_1525940,Human_Splice_Rec_1525942 RMVar_hsa_circ_31949,RMVar_hsa_circ_102591,RMVar_hsa_circ_167302 113670 RMVar_ID_113670 Human_SNP_ID_822634037 m1A Human chr14 - 69768676 69768676 69768676 GTCCCAGGGTTATCTAGTTACACAGGAATCTCACCTTTCACTACAGAGTTCTTTTCCATCAAGCT GTCCCAGGGTTATCTAGTTACACAGGAATCTCGCCTTTCACTACAGAGTTCTTTTCCATCAAGCT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:69768651..69768675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 7 liver 113671 RMVar_ID_113671 Human_SNP_ID_822641900 m1A Human chr14 - 24237561 24237561 24237561 AATCATCCTTCTGTGCCCTCAAGCTCCTTACCAAAAGCCTTGGCCACATCCCCAGGACAGCTGCA AATCATCCTTCTGTGCCCTCAAGCTCCTTACCGAAAGCCTTGGCCACATCCCCAGGACAGCTGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24237102..24237612 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 12 uterus 113672 RMVar_ID_113672 Human_SNP_ID_822645313 m1A Human chr14 - 64481771 64481771 64481771 TCTCTGCTGTACTTCTGTGTTTGTATGGTTGGACATTTTGAAAACTGGTGAGATTGCACAGTCCC TCTCTGCTGTACTTCTGTGTTTGTATGGTTGGTCATTTTGAAAACTGGTGAGATTGCACAGTCCC T A ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10133848 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1086221 GWAS_ID_8759,GWAS_ID_8760,GWAS_ID_8761,GWAS_ID_8762,GWAS_ID_8763,GWAS_ID_8764,GWAS_ID_8765,GWAS_ID_8766,GWAS_ID_8767,GWAS_ID_8768,GWAS_ID_8769,GWAS_ID_8770,GWAS_ID_8771,GWAS_ID_8772,GWAS_ID_8773 113673 RMVar_ID_113673 Human_SNP_ID_822684546 m1A Human chr14 - 91293473 91293473 91293473 TGGCAGGTGAGGATGGGAAGGTGAGCTGTGGCAGGTGAGGATGGGAAGGTGGACCGTGGCAGGTG TGGCAGGTGAGGATGGGAAGGTGAGCTGTGGCGGGTGAGGATGGGAAGGTGGACCGTGGCAGGTG T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:91292955..91293583;chr14:91292946..91293621;chr14:91293411..91293538 26863196 MeRIP-seq:(Medium) rs61988373 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 2 brain Human_RBP_ID_812893,Human_RBP_ID_1085694,Human_RBP_ID_8180968,Human_RBP_ID_9418055 RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 113674 RMVar_ID_113674 Human_SNP_ID_822684971 m1A Human chr14 - 77025674 77025674 77025674 AAGTGCACCCCCAAAACATTCCGGATTCCCCCATGGCCAACAGCGGACCCCTCTGCTGCACCATT AAGTGCACCCCCAAAACATTCCGGATTCCCCCGTGGCCAACAGCGGACCCCTCTGCTGCACCATT T C IRF2BPL Ensembl:ENSG00000119669 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:77025623..77026001 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_8077774,Human_RBP_ID_8410749,Human_RBP_ID_27229091,Human_RBP_ID_27433029 113675 RMVar_ID_113675 Human_SNP_ID_822685452 m1A Human chr14 + 39180761 39180759 39180761 GGAAATAGCGATTGTTCATAGTGATGCAGAGAAAGAACAGGAGGAGGAAGAACAAAAACAGGAAA GGAAATAGCGATTGTTCATAGTGATGCAGAG__AGAACAGGAGGAGGAAGAACAAAAACAGGAAA GAA G PNN Ensembl:ENSG00000100941 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr14:39180501..39181025 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 BRCA 1 - Human_RBP_ID_197009,Human_RBP_ID_1493523,Human_RBP_ID_1818951,Human_RBP_ID_2413681,Human_RBP_ID_3449301,Human_RBP_ID_5563184,Human_RBP_ID_6347878,Human_RBP_ID_9345082,Human_RBP_ID_9766274,Human_RBP_ID_12329732,Human_RBP_ID_17651177,Human_RBP_ID_18650409,Human_RBP_ID_22737494,Human_RBP_ID_22923565,Human_RBP_ID_23118230,Human_RBP_ID_23272471,Human_RBP_ID_23621887,Human_RBP_ID_24543670,Human_RBP_ID_26325020 Human_miRNA_ID_1132646 RMVar_hsa_circ_166124 113676 RMVar_ID_113676 Human_SNP_ID_822699129 m1A Human chr14 + 24138116 24138116 24138116 TGAGGATGGTAACAATTTTGGAGTGGCTGTCCAGGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT TGAGGATGGTAACAATTTTGGAGTGGCTGTCCTGGTGAGAGCGCTGCCCCACTTCCCTGCTCTTT A T PSME1 Ensembl:ENSG00000092010 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:24138026..24138125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_9368605,Human_RBP_ID_17856384,Human_RBP_ID_19063760,Human_RBP_ID_26324627 Human_Splice_Rec_1498046,Human_Splice_Rec_1498047,Human_Splice_Rec_1498064,Human_Splice_Rec_1498065,Human_Splice_Rec_1498078,Human_Splice_Rec_1498088,Human_Splice_Rec_1498104,Human_Splice_Rec_1498105,Human_Splice_Rec_1498120,Human_Splice_Rec_1498121,Human_Splice_Rec_1498138,Human_Splice_Rec_1498148,Human_Splice_Rec_1498149,Human_Splice_Rec_1498154,Human_Splice_Rec_1498155 RMVar_hsa_circ_90904,RMVar_hsa_circ_83404,RMVar_hsa_circ_165352,RMVar_hsa_circ_96832,RMVar_hsa_circ_165353,RMVar_hsa_circ_335698,RMVar_hsa_circ_165354,RMVar_hsa_circ_165355 113677 RMVar_ID_113677 Human_SNP_ID_822708189 m1A Human chr14 - 56118628 56118628 56118628 GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGACGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT GGAGCCCCGCTCGGCCGCCGACGCCGCCGCCGCCGCCGCCGCCTCCGCCGCGATCCCCGCCGAGT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:56118370..56118656 26863196 MeRIP-seq:(Medium) rs531124616 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 113678 RMVar_ID_113678 Human_SNP_ID_822711929 m1A Human chr14 - 70907613 70907613 70907613 GAGGCGGCGAGCGGCGGGGCGGAGGACGGCGGAGAGGAGGAGACCGGCCTTCTGAGAGCCGCCGC GAGGCGGCGAGCGGCGGGGCGGAGGACGGCGGGGAGGAGGAGACCGGCCTTCTGAGAGCCGCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr14:70907515..70907651 26863410 MeRIP-seq:(Medium) rs148523058 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 1 brain 113679 RMVar_ID_113679 Human_SNP_ID_822736465 m1A Human chr14 + 105226275 105226275 105226275 TTGGTTACCTTCAACCTCCTCCAGTTTTTTTGACAGGACTTGTTCAAGCTGAAAGGGAACAGGGC TTGGTTACCTTCAACCTCCTCCAGTTTTTTTGGCAGGACTTGTTCAAGCTGAAAGGGAACAGGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:105226136..105226718 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 18 large intestine 113680 RMVar_ID_113680 Human_SNP_ID_822744066 m1A Human chr14 + 105093921 105093921 105093921 GAGCGGAGGGTCCAGGCTAGGCTGGGGGAGCGAGAGGCGAGGGCGGAGCCGCGGAGGTGTGGGCG GAGCGGAGGGTCCAGGCTAGGCTGGGGGAGCGTGAGGCGAGGGCGGAGCCGCGGAGGTGTGGGCG A T LINC02298 Ensembl:ENSG00000257556 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:105093770..105094136 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - 113681 RMVar_ID_113681 Human_SNP_ID_822764622 m1A Human chr14 - 104176825 104176825 104176825 TGGGCCTCGGGAGGAAGCCCGCCTTGGGAGCCAGACCCTTCTTGCTGGTGGGGGAGGCCTTCAGG TGGGCCTCGGGAGGAAGCCCGCCTTGGGAGCCGGACCCTTCTTGCTGGTGGGGGAGGCCTTCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104176775..104176889 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 113682 RMVar_ID_113682 Human_SNP_ID_822768767 m1A Human chr14 - 37594950 37594950 37594950 TGGCTCCAGGATGTTAGGAACTGTGAAGATGGAAGGGCATGAAACCAGCGACTGGAACAGCTACT TGGCTCCAGGATGTTAGGAACTGTGAAGATGGGAGGGCATGAAACCAGCGACTGGAACAGCTACT T C FOXA1 Ensembl:ENSG00000129514 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:37594823..37595111 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_1493421,Human_RBP_ID_1818817,Human_RBP_ID_3448998,Human_RBP_ID_4307894,Human_RBP_ID_5463724,Human_RBP_ID_6347125,Human_RBP_ID_17651631,Human_RBP_ID_18650261 Human_Splice_Rec_1508519,Human_Splice_Rec_1508523,Human_Splice_Rec_1508527 113683 RMVar_ID_113683 Human_SNP_ID_822768775 m1A Human chr14 - 37594950 37594950 37594950 TGGCTCCAGGATGTTAGGAACTGTGAAGATGGAAGGGCATGAAACCAGCGACTGGAACAGCTACT TGGCTCCAGGATGTTAGGAACTGTGAAGATGGTAGGGCATGAAACCAGCGACTGGAACAGCTACT T A FOXA1 Ensembl:ENSG00000129514 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:37594823..37595111 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-positive_carcinoma 1 breast Human_RBP_ID_1493421,Human_RBP_ID_1818817,Human_RBP_ID_3448998,Human_RBP_ID_4307894,Human_RBP_ID_5463724,Human_RBP_ID_6347125,Human_RBP_ID_17651631,Human_RBP_ID_18650261 Human_Splice_Rec_1508519,Human_Splice_Rec_1508523,Human_Splice_Rec_1508527 113684 RMVar_ID_113684 Human_SNP_ID_822774507 m1A Human chr14 - 50760170 50760170 50760170 TGCTCAAGGAGGCACATCATGAGGCCACTTGCAGGCATGAGGAGGAGAAAAAACAACTGCAAGTG TGCTCAAGGAGGCACATCATGAGGCCACTTGCGGGCATGAGGAGGAGAAAAAACAACTGCAAGTG T C NIN Ensembl:ENSG00000100503 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:50759989..50760318 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine RMVar_hsa_circ_46869,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_324799,RMVar_hsa_circ_64625,RMVar_hsa_circ_166564,RMVar_hsa_circ_23643,RMVar_hsa_circ_23989,RMVar_hsa_circ_298344,RMVar_hsa_circ_57623,RMVar_hsa_circ_72339,RMVar_hsa_circ_166571,RMVar_hsa_circ_266035,RMVar_hsa_circ_359044,RMVar_hsa_circ_13706,RMVar_hsa_circ_294758,RMVar_hsa_circ_339517,RMVar_hsa_circ_166572 113685 RMVar_ID_113685 Human_SNP_ID_822777526 m1A Human chr14 + 75084595 75084595 75084595 ACTAGAGGCTGGGTCTACAGGAGTCTGTTCCCAGGAGGCACCAGGAATCTGAATCTAAGTCAGGC ACTAGAGGCTGGGTCTACAGGAGTCTGTTCCCGGGAGGCACCAGGAATCTGAATCTAAGTCAGGC A G ZC2HC1C Ensembl:ENSG00000119703 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:75084545..75084918 32194978 MeRIP-seq:(Medium) rs916880902 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 113686 RMVar_ID_113686 Human_SNP_ID_822779511 m1A Human chr14 + 24007119 24007119 24007119 ACTGTCTGGAGCGGGCTCGCCTCTGCGGCGGCACTCACCGCCCGGGCTTTACTGAAGCGGAGTCT ACTGTCTGGAGCGGGCTCGCCTCTGCGGCGGCCCTCACCGCCCGGGCTTTACTGAAGCGGAGTCT A C AL136419.1 Ensembl:ENSG00000285467 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:24007082..24007166;chr14:24007091..24007175;chr14:24007040..24007161 26863196 MeRIP-seq:(Medium) rs555880908 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_5418060 113687 RMVar_ID_113687 Human_SNP_ID_822792356 m1A Human chr14 - 75124174 75124174 75124174 GTGGAAGGAAGTCGATTTGACCCGGCTGTCTGAGAAGGAACGTCGTGATGCCTTGAATGAGATTG GTGGAAGGAAGTCGATTTGACCCGGCTGTCTGGGAAGGAACGTCGTGATGCCTTGAATGAGATTG T C NEK9 Ensembl:ENSG00000119638 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:75124124..75127003 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_1499624,Human_RBP_ID_5563497,Human_RBP_ID_8410390,Human_RBP_ID_12424252,Human_RBP_ID_23636929,Human_RBP_ID_26326286 Human_Splice_Rec_1537088,Human_Splice_Rec_1537168,Human_Splice_Rec_1537214,Human_Splice_Rec_1537226,Human_Splice_Rec_1537234 RMVar_hsa_circ_337374,RMVar_hsa_circ_373485,RMVar_hsa_circ_106406,RMVar_hsa_circ_167988,RMVar_hsa_circ_125683,RMVar_hsa_circ_167987,RMVar_hsa_circ_299039,RMVar_hsa_circ_167989,RMVar_hsa_circ_309894,RMVar_hsa_circ_167996,RMVar_hsa_circ_292386,RMVar_hsa_circ_168002,RMVar_hsa_circ_353739,RMVar_hsa_circ_373442,RMVar_hsa_circ_168006,RMVar_hsa_circ_291746,RMVar_hsa_circ_344495,RMVar_hsa_circ_309996,RMVar_hsa_circ_168007,RMVar_hsa_circ_117853,RMVar_hsa_circ_334276,RMVar_hsa_circ_291648,RMVar_hsa_circ_168014,RMVar_hsa_circ_168016,RMVar_hsa_circ_288968,RMVar_hsa_circ_168022,RMVar_hsa_circ_168018,RMVar_hsa_circ_168021,RMVar_hsa_circ_289113,RMVar_hsa_circ_284580,RMVar_hsa_circ_168023,RMVar_hsa_circ_273389 113688 RMVar_ID_113688 Human_SNP_ID_822799121 m1A Human chr14 - 91272352 91272352 91272352 ACAAATAATCCACGTCAGCATGGGGACCAATTAGGATGCAATGACAAACTGACTTCCCCCAAAGC ACAAATAATCCACGTCAGCATGGGGACCAATTCGGATGCAATGACAAACTGACTTCCCCCAAAGC T G CCDC88C Ensembl:ENSG00000015133 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12878426 Functional Loss SNV ICGC 33..33 33 LUSC 2 - GWAS_ID_7358 RMVar_hsa_circ_268120 113689 RMVar_ID_113689 Human_SNP_ID_822835151 m1A Human chr14 - 74809526 74809523 74809526 GAAGTTTGTGGCTTTATCACTGGAGGAGGAGGAGGTAGAGGTGGAGGAGGTGGAGGTGGTGGTAT GAAGTTTGTGGCTTTATCACTGGAGGAGGAGG___TAGAGGTGGAGGAGGTGGAGGTGGTGGTAT ACCT A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:74809426..74809938 32194978 MeRIP-seq:(Medium) rs773250816 Functional Loss DEL ICGC 33..35 33 STAD 1 - RMVar_hsa_circ_167948 113690 RMVar_ID_113690 Human_SNP_ID_822850501 m1A Human chr14 + 67695699 67695699 67695699 GAAGGAGGAGCAACAGCGGGAACATGAGCTCAACCATCTCTGCCGGCTGCAGCGGCACCAGAGCG GAAGGAGGAGCAACAGCGGGAACATGAGCTCATCCATCTCTGCCGGCTGCAGCGGCACCAGAGCG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:67695605..67695704 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 113691 RMVar_ID_113691 Human_SNP_ID_822850766 m1A Human chr14 + 65102406 65102406 65102406 GGCGGGGAGGGGAAGGGGTGAAGGGGAGGGGGAAGTCACCGACAACAACAAGCCGAGTCCCCCCC GGCGGGGAGGGGAAGGGGTGAAGGGGAGGGGGGAGTCACCGACAACAACAAGCCGAGTCCCCCCC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:65102301..65102525 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 13 uterus 113692 RMVar_ID_113692 Human_SNP_ID_822853495 m1A Human chr14 + 60648998 60648998 60648998 AACTGGTGGCTCTCCAGGATCTTGTAGAGCTCACGGAAGTTGCCGCGGTGGAAGGCGACCACCGC AACTGGTGGCTCTCCAGGATCTTGTAGAGCTCGCGGAAGTTGCCGCGGTGGAAGGCGACCACCGC A G SALRNA1 RNACentral:URS00008B9496 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:60648951..60649000 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 113693 RMVar_ID_113693 Human_SNP_ID_822893020 m1A Human chr14 + 76763116 76763116 76763116 GAGAGAAGGTGGCGCAACGGATCCGTGGGGCCACAGACCTGCCCAAGGTGAGACACACGGGTCAG GAGAGAAGGTGGCGCAACGGATCCGTGGGGCCTCAGACCTGCCCAAGGTGAGACACACGGGTCAG A T VASH1 Ensembl:ENSG00000071246 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:76762833..76769981 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_1538273,Human_Splice_Rec_1538285 113694 RMVar_ID_113694 Human_SNP_ID_822912226 m1A Human chr14 + 68877226 68877226 68877226 CGGTTGGGGTCCACAATGCTCATGATGCGGGCAAATTCTGCTTCTCCCTGGAGGGAACAGCCAAA CGGTTGGGGTCCACAATGCTCATGATGCGGGCGAATTCTGCTTCTCCCTGGAGGGAACAGCCAAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:68875140..68877225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 113695 RMVar_ID_113695 Human_SNP_ID_822929859 m1A Human chr14 + 24441766 24441766 24441766 CCAGCAATTGGGTGGTCTCTAGGCGGCTGCCGATTACCTCTTTTTGGAAGGTTTCATTCCATCTG CCAGCAATTGGGTGGTCTCTAGGCGGCTGCCGCTTACCTCTTTTTGGAAGGTTTCATTCCATCTG A C KHNYN Ensembl:ENSG00000100441 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:24441716..24441807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 6 pancreas 113696 RMVar_ID_113696 Human_SNP_ID_822955930 m1A Human chr14 + 23321778 23321778 23321778 CCCGGCAGCCAAGAGGAGGAGGAGGAGCCGGGACTGGTCGAGGGTGACCCGGGGGACGGCGCCAT CCCGGCAGCCAAGAGGAGGAGGAGGAGCCGGGGCTGGTCGAGGGTGACCCGGGGGACGGCGCCAT A G PABPN1,BCL2L2-PABPN1 Ensembl:ENSG00000100836,Ensembl:ENSG00000258643 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:23321401..23321889;chr14:23321388..23323114;chr14:23308042..23325742;chr14:23308050..23323475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4404,Human_RBP_ID_3467656,Human_RBP_ID_3944430,Human_RBP_ID_4289384,Human_RBP_ID_5112544,Human_RBP_ID_5140738,Human_RBP_ID_6334752,Human_RBP_ID_9369742,Human_RBP_ID_12301927,Human_RBP_ID_18418063,Human_RBP_ID_22532579,Human_RBP_ID_23113652 Human_Splice_Rec_1495543,Human_Splice_Rec_1495555 113697 RMVar_ID_113697 Human_SNP_ID_823017035 m1A Human chr14 + 50118681 50118681 50118681 ATGGACAGTTTATAAAGTGTTCTGGAGGCCGAAGGGGAACTGGTGGAGGGGTATCAGGAAGAGGA ATGGACAGTTTATAAAGTGTTCTGGAGGCCGATGGGGAACTGGTGGAGGGGTATCAGGAAGAGGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:50118632..50118739 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - 113698 RMVar_ID_113698 Human_SNP_ID_823052020 m1A Human chr14 - 105221863 105221863 105221863 GTCCAGCTTGTGTGGCGAGGAGGACACAGAGGACGAGGAGCTGGAAGCCGCGGCCAGCCACCTGA GTCCAGCTTGTGTGGCGAGGAGGACACAGAGGCCGAGGAGCTGGAAGCCGCGGCCAGCCACCTGA T G BRF1 Ensembl:ENSG00000185024 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr14:105221756..105221915;chr14:105221705..105221932;chr14:105221765..105221965;chr14:105221729..105221926 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_813385,Human_RBP_ID_883110,Human_RBP_ID_19064478,Human_RBP_ID_22926519,Human_RBP_ID_26325554,Human_RBP_ID_27809218 Human_Splice_Rec_1561442,Human_Splice_Rec_1561474,Human_Splice_Rec_1561508,Human_Splice_Rec_1561556,Human_Splice_Rec_1561628,Human_Splice_Rec_1561662,Human_Splice_Rec_1561690,Human_Splice_Rec_1561714,Human_Splice_Rec_1561726 RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_108620,RMVar_hsa_circ_169696,RMVar_hsa_circ_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_265061 113699 RMVar_ID_113699 Human_SNP_ID_823052671 m1A Human chr14 - 51047179 51047179 51047179 GGAATTCTAGGAAAAAAGGGACAGAATGTTAAAAGGCCCAGAGACTTAAAGCCACATAGGACCTT GGAATTCTAGGAAAAAAGGGACAGAATGTTAAGAGGCCCAGAGACTTAAAGCCACATAGGACCTT T C TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:51047113..51047226 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver 113700 RMVar_ID_113700 Human_SNP_ID_823055382 m1A Human chr14 - 75176476 75176476 75176476 CGGCCCCAGATTGGTCCTTGCCATCTCCTTCCATCTGCCCATTAACTCTCGCAAGTGCCTCCGTG CGGCCCCAGATTGGTCCTTGCCATCTCCTTCCGTCTGCCCATTAACTCTCGCAAGTGCCTCCGTG T C TMED10 Ensembl:ENSG00000170348 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:75176426..75176625 26863196 MeRIP-seq:(Medium) rs753647635 Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_452123,Human_RBP_ID_757358,Human_RBP_ID_813066,Human_RBP_ID_883993,Human_RBP_ID_1499707,Human_RBP_ID_2426985,Human_RBP_ID_4308014,Human_RBP_ID_5418298,Human_RBP_ID_5439289,Human_RBP_ID_5463559,Human_RBP_ID_8410443,Human_RBP_ID_18656927,Human_RBP_ID_22045080,Human_RBP_ID_22438792,Human_RBP_ID_24410721,Human_RBP_ID_24472497,Human_RBP_ID_26808134,Human_RBP_ID_27432938 Human_miRNA_ID_2619236 RMVar_hsa_circ_119536,RMVar_hsa_circ_168025 113701 RMVar_ID_113701 Human_SNP_ID_823069617 m1A Human chr14 - 102010435 102010435 102010436 TAACGAACCTCTTGTTCAGGGAGATTTTCAGCAATTTCTCCTTCATCAACTGCTTCCCCTCGTTC TAACGAACCTCTTGTTCAGGGAGATTTTCAGATATTTCTCCTTCATCAACTGCTTCCCCTCGTTC TG AT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102010384..102010467 26863196 MeRIP-seq:(Medium) - Functional Loss MNV ICGC 32..33 33 MELA 1 - 113702 RMVar_ID_113702 Human_SNP_ID_823071194 m1A Human chr14 - 103519991 103519991 103519991 GGTGGGCGGGGTCTTCGACGTCTCCAACGCTGACCGCCTGGGCTTCTCAGAGGTGGAGCTGGTGC GGTGGGCGGGGTCTTCGACGTCTCCAACGCTGCCCGCCTGGGCTTCTCAGAGGTGGAGCTGGTGC T G CKB Ensembl:ENSG00000166165 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr14:103519727..103520327;chr14:103519742..103520231 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain Human_RBP_ID_441800,Human_RBP_ID_757343,Human_RBP_ID_883328,Human_RBP_ID_1273925,Human_RBP_ID_1360881,Human_RBP_ID_1488934,Human_RBP_ID_1815360,Human_RBP_ID_3442689,Human_RBP_ID_4283181,Human_RBP_ID_5112483,Human_RBP_ID_6327735,Human_RBP_ID_8250003,Human_RBP_ID_8399847,Human_RBP_ID_8793102,Human_RBP_ID_12282474,Human_RBP_ID_17246609,Human_RBP_ID_17361481,Human_RBP_ID_17478381,Human_RBP_ID_17651128,Human_RBP_ID_17845182,Human_RBP_ID_18646028,Human_RBP_ID_22355364,Human_RBP_ID_22438605,Human_RBP_ID_23126599,Human_RBP_ID_26920720,Human_RBP_ID_27224133 Human_Splice_Rec_1558640,Human_Splice_Rec_1558644,Human_Splice_Rec_1558648,Human_Splice_Rec_1558654,Human_Splice_Rec_1558668,Human_Splice_Rec_1558674,Human_Splice_Rec_1558678 Human_miRNA_ID_208071 RMVar_hsa_circ_169545,RMVar_hsa_circ_96084,RMVar_hsa_circ_126066,RMVar_hsa_circ_92404,RMVar_hsa_circ_169546,RMVar_hsa_circ_169544 113703 RMVar_ID_113703 Human_SNP_ID_823074913 m1A Human chr14 - 32484957 32484957 32484957 TCAACGCTTCAATCTACTTCTCCCGCCGCAGGAAAAAAAGGCGGGAGAAGCCCCGCCAGGTTTGA TCAACGCTTCAATCTACTTCTCCCGCCGCAGGGAAAAAAGGCGGGAGAAGCCCCGCCAGGTTTGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:32484922..32485058 26863196 MeRIP-seq:(Medium) rs796769414 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_5236190 113704 RMVar_ID_113704 Human_SNP_ID_823078132 m1A Human chr14 + 104701401 104701401 104701401 TCGGTGAAGGAGGGCGCACAGCGCAAGTGGGCAGCGCTGAAGGAGAAGCTGGGGCCACAGGATTC TCGGTGAAGGAGGGCGCACAGCGCAAGTGGGCGGCGCTGAAGGAGAAGCTGGGGCCACAGGATTC A G INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr14:104701376..104701400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 8 caecum,large intestine Human_RBP_ID_4309117,Human_RBP_ID_9369568,Human_RBP_ID_18981063 Human_Splice_Rec_1560312,Human_Splice_Rec_1560352,Human_Splice_Rec_1560394 113705 RMVar_ID_113705 Human_SNP_ID_823087059 m1A Human chr14 + 104707948 104707948 104707948 GGGTCCCCAGCCATCGGCGGGTGAACCCACCCACACTGCGCATGAAGAAGCTGAACTGGCAGAAG GGGTCCCCAGCCATCGGCGGGTGAACCCACCCCCACTGCGCATGAAGAAGCTGAACTGGCAGAAG A C INF2 Ensembl:ENSG00000203485 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:104707661..104708349 32194978 MeRIP-seq:(Medium) rs1334835727 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 24 head and neck Human_RBP_ID_5563005,Human_RBP_ID_18981082 Human_Splice_Rec_1560325,Human_Splice_Rec_1560365,Human_Splice_Rec_1560401,Human_Splice_Rec_1560431 RMVar_hsa_circ_58272,RMVar_hsa_circ_169640,RMVar_hsa_circ_97495,RMVar_hsa_circ_124679,RMVar_hsa_circ_169641,RMVar_hsa_circ_169642,RMVar_hsa_circ_114585 113706 RMVar_ID_113706 Human_SNP_ID_823095833 m1A Human chr14 - 49893682 49893682 49893682 GGGGCATTCAGGTGTCCCGGGTCCCCTCAGCCAACAACGCCGCCGCCGCCGCGAAACCGAAACGA GGGGCATTCAGGTGTCCCGGGTCCCCTCAGCCTACAACGCCGCCGCCGCCGCGAAACCGAAACGA T A lnc-NEMF-4 RNACentral:URS0000D59A1E lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:49893316..49893725 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 113707 RMVar_ID_113707 Human_SNP_ID_823108664 m1A Human chr14 - 104938050 104938050 104938050 TGGGACCAAATGAAGGCTGAGAGGTATGGCTCATCAGTACAAGAGAGATGCAAAAAACTAAGTTG TGGGACCAAATGAAGGCTGAGAGGTATGGCTCTTCAGTACAAGAGAGATGCAAAAAACTAAGTTG T A AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:104937838..104938149 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung RMVar_hsa_circ_77373,RMVar_hsa_circ_120453,RMVar_hsa_circ_118063,RMVar_hsa_circ_122947,RMVar_hsa_circ_169673,RMVar_hsa_circ_113263,RMVar_hsa_circ_119278,RMVar_hsa_circ_98850,RMVar_hsa_circ_169674,RMVar_hsa_circ_169676,RMVar_hsa_circ_169678,RMVar_hsa_circ_169680,RMVar_hsa_circ_76020,RMVar_hsa_circ_169679,RMVar_hsa_circ_169677,RMVar_hsa_circ_169675 113708 RMVar_ID_113708 Human_SNP_ID_823146865 m1A Human chr14 - 21499552 21499552 21499552 GAAATTATTTGGGTGAAGACAAATCAACTGCAACGCATCATTCGGACAGGCCGTACAGGTCACTG GAAATTATTTGGGTGAAGACAAATCAACTGCACCGCATCATTCGGACAGGCCGTACAGGTCACTG T G METTL3 Ensembl:ENSG00000165819 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:21499457..21499577 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1816688,Human_RBP_ID_3944801,Human_RBP_ID_8401725,Human_RBP_ID_12297776,Human_RBP_ID_18206849,Human_RBP_ID_18435697,Human_RBP_ID_18528266,Human_RBP_ID_18979187,Human_RBP_ID_22184814,Human_RBP_ID_22922337,Human_RBP_ID_23208476 Human_Splice_Rec_1492332,Human_Splice_Rec_1492333,Human_Splice_Rec_1492350,Human_Splice_Rec_1492351,Human_Splice_Rec_1492366,Human_Splice_Rec_1492367,Human_Splice_Rec_1492378,Human_Splice_Rec_1492396,Human_Splice_Rec_1492412,Human_Splice_Rec_1492426,Human_Splice_Rec_1492427 RMVar_hsa_circ_32592,RMVar_hsa_circ_126379,RMVar_hsa_circ_45235,RMVar_hsa_circ_165213 113709 RMVar_ID_113709 Human_SNP_ID_823168824 m1A Human chr14 - 58353711 58353711 58353711 CTTTCACTTTGGTTCCTGTTAGGCAGGGTTCCATGTCTTCCTCATCTTCCTCTCCTTCAGAGTCA CTTTCACTTTGGTTCCTGTTAGGCAGGGTTCCCTGTCTTCCTCATCTTCCTCTCCTTCAGAGTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:58353619..58353723 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 5 bladder,urinary tract 113710 RMVar_ID_113710 Human_SNP_ID_823174850 m1A Human chr14 + 67659860 67659860 67659860 TTAGCAAGGTCCTTCCGGTAGTTTCGAAGCTTAGACATCATGGGGTTTCGGAAAGACAGGGGTGC TTAGCAAGGTCCTTCCGGTAGTTTCGAAGCTTGGACATCATGGGGTTTCGGAAAGACAGGGGTGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:67651078..67659974 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 113711 RMVar_ID_113711 Human_SNP_ID_823180797 m1A Human chr14 + 52858176 52858176 52858176 TTTCAATTCATGGCCCTAAGGAATGTGTGACAAATTCAAGTTTATTATATCATAACATGATAGAT TTTCAATTCATGGCCCTAAGGAATGTGTGACACATTCAAGTTTATTATATCATAACATGATAGAT A C AL139317.5 Ensembl:ENSG00000285664 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:52857964..52858213 32194978 MeRIP-seq:(Medium) rs182640915 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 113712 RMVar_ID_113712 Human_SNP_ID_823182699 m1A Human chr14 + 92121460 92121460 92121460 TCAGAAAACCCTTTCCAAAAGCTCCGGCCCGGAAATCCCATCCTCCACCCGAAGAAAACCCCATT TCAGAAAACCCTTTCCAAAAGCTCCGGCCCGGCAATCCCATCCTCCACCCGAAGAAAACCCCATT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:92121451..92121944 26863196 MeRIP-seq:(Medium) rs7143338 Functional Loss SNV ICGC 33..33 33 LUSC 1 - GWAS_ID_7361,GWAS_ID_7362,GWAS_ID_7363,GWAS_ID_7364,GWAS_ID_7365,GWAS_ID_7366,GWAS_ID_7367 113713 RMVar_ID_113713 Human_SNP_ID_823194826 m1A Human chr14 + 35107252 35107252 35107252 GTAATCCCAACACCCAGTGATAACTACAGTTTACATTTTAGTGTCTATAAGAGTTAATATAATAT GTAATCCCAACACCCAGTGATAACTACAGTTTCCATTTTAGTGTCTATAAGAGTTAATATAATAT A C FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr14:35107237..35107407 26863410 MeRIP-seq:(Medium) rs10132769 Functional Loss SNV ICGC 33..33 33 COCA 3 - 113714 RMVar_ID_113714 Human_SNP_ID_823271996 m1A Human chr14 - 65279277 65279277 65279277 CCCGCTTTGTACCAACTGCTATATCTGGGACAATGCCGTCCATGGCACACACAGCAGACCCGTGG CCCGCTTTGTACCAACTGCTATATCTGGGACATTGCCGTCCATGGCACACACAGCAGACCCGTGG T A AL355076.2 Ensembl:ENSG00000258760 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:65279271..65279336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113715 RMVar_ID_113715 Human_SNP_ID_823273955 m1A Human chr14 - 103057475 103057475 103057475 GCCGCTCCTAGTCTGCGGCGGCGGCGGCGGGGAGGGCGCGGCCGCGGGCGGGGCTGAGGGCGGCG GCCGCTCCTAGTCTGCGGCGGCGGCGGCGGGGGGGGCGCGGCCGCGGGCGGGGCTGAGGGCGGCG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr14:103057426..103057540;chr14:103057388..103057571 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - 113716 RMVar_ID_113716 Human_SNP_ID_823295538 m1A Human chr14 - 96282273 96282273 96282273 ACAAAGCAATATTCTTTTGTATCTGCAAATGCATCAGCTGGACATACCAATTGGTATCAAATAGA ACAAAGCAATATTCTTTTGTATCTGCAAATGCGTCAGCTGGACATACCAATTGGTATCAAATAGA T C ATG2B Ensembl:ENSG00000066739 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7150634 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_7370,GWAS_ID_7371,GWAS_ID_7372,GWAS_ID_7373,GWAS_ID_7374,GWAS_ID_7375,GWAS_ID_7376,GWAS_ID_7377,GWAS_ID_7378,GWAS_ID_7379,GWAS_ID_7380,GWAS_ID_7381,GWAS_ID_7382,GWAS_ID_7383,GWAS_ID_7384,GWAS_ID_7385,GWAS_ID_7386,GWAS_ID_7387 RMVar_hsa_circ_90457,RMVar_hsa_circ_268876,RMVar_hsa_circ_168857 113717 RMVar_ID_113717 Human_SNP_ID_823296176 m1A Human chr14 - 73712918 73712918 73712918 GAAGGCGCTTGAGCAGGTGTTTGGGAGCGTTGAGAGCTCTAGGGATGCCCAGATCAAATTTCTGA GAAGGCGCTTGAGCAGGTGTTTGGGAGCGTTGGGAGCTCTAGGGATGCCCAGATCAAATTTCTGA T C PNMA1 Ensembl:ENSG00000176903 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:73712776..73713000 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_1498940,Human_RBP_ID_6382972,Human_RBP_ID_8796135,Human_RBP_ID_12415382 113718 RMVar_ID_113718 Human_SNP_ID_823310682 m1A Human chr14 - 104884313 104884313 104884313 AACCTTCTCGGGGCTGGGCCGGGCGGCCGGGGAGCTCTCCCGCAGACACTGGGCCATGAAGTCCT AACCTTCTCGGGGCTGGGCCGGGCGGCCGGGGTGCTCTCCCGCAGACACTGGGCCATGAAGTCCT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:104884262..104884374 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113719 RMVar_ID_113719 Human_SNP_ID_823311210 m1A Human chr14 - 39176030 39176030 39176030 AAATCAGTGCAAAATCATATGTAGACACACACAGTCGCACCCAAATACTTTCAGAGATGTGGATC AAATCAGTGCAAAATCATATGTAGACACACACTGTCGCACCCAAATACTTTCAGAGATGTGGATC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:39176028..39176197 26863196 MeRIP-seq:(Medium) rs1486572897 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,PRAD 4 prostate 113720 RMVar_ID_113720 Human_SNP_ID_823322563 m1A Human chr14 + 104729893 104729893 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCGTGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG A G ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs80097179 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 113721 RMVar_ID_113721 Human_SNP_ID_823322566 m1A Human chr14 + 104729893 104729893 104729893 GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCATGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG GTCGGCGTCGTGGGGAGGAGCGTGGCGTCGGCCTGGTGGGGAGGAGCTGTGGGGTGGCAACCCAG A C ADSS1 Ensembl:ENSG00000185100 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:104729860..104730179 26863196 MeRIP-seq:(Medium) rs80097179 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 10 liver,head and neck,large intestine Human_RBP_ID_1065739,Human_RBP_ID_8181085,Human_RBP_ID_18457742,Human_RBP_ID_22711198 Human_Splice_Rec_1560503 113722 RMVar_ID_113722 Human_SNP_ID_823333260 m1A Human chr14 - 20458176 20458176 20458176 GGTAGCCCTGGGGGTTCCCCTCCCTCTTGTGCACCATTAGGACTTTGCTGCTGCTATTGCACTTC GGTAGCCCTGGGGGTTCCCCTCCCTCTTGTGCGCCATTAGGACTTTGCTGCTGCTATTGCACTTC T C PIP4P1 Ensembl:ENSG00000165782 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr14:20458112..20458275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_442736,Human_RBP_ID_757720,Human_RBP_ID_1171364,Human_RBP_ID_5112622,Human_RBP_ID_8401148,Human_RBP_ID_12290930,Human_RBP_ID_18272123,Human_RBP_ID_23615075,Human_RBP_ID_26431551 113723 RMVar_ID_113723 Human_SNP_ID_823342580 m1A Human chr14 - 50821982 50821982 50821982 GAGCTGTTTGACAGTTTTGACACGACGGGCACAGGGTCCCTGGGGCAGGAGGAACTCACCGACCT GAGCTGTTTGACAGTTTTGACACGACGGGCACCGGGTCCCTGGGGCAGGAGGAACTCACCGACCT T G NIN Ensembl:ENSG00000100503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:50821938..50830574 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas Human_RBP_ID_881814,Human_RBP_ID_4308789,Human_RBP_ID_6354011,Human_RBP_ID_8797831,Human_RBP_ID_18980617 Human_Splice_Rec_1513002,Human_Splice_Rec_1513062,Human_Splice_Rec_1513122,Human_Splice_Rec_1513178,Human_Splice_Rec_1513294,Human_Splice_Rec_1513384,Human_Splice_Rec_1513440,Human_Splice_Rec_1513532,Human_Splice_Rec_1513606,Human_Splice_Rec_1513648,Human_Splice_Rec_1513654 Human_miRNA_ID_1950765,Human_miRNA_ID_1952051,Human_miRNA_ID_2151727,Human_miRNA_ID_2420196 RMVar_hsa_circ_46869,RMVar_hsa_circ_265903,RMVar_hsa_circ_123325,RMVar_hsa_circ_166581,RMVar_hsa_circ_95748,RMVar_hsa_circ_166580,RMVar_hsa_circ_279841,RMVar_hsa_circ_166583,RMVar_hsa_circ_64333,RMVar_hsa_circ_166584,RMVar_hsa_circ_308919,RMVar_hsa_circ_308205 113724 RMVar_ID_113724 Human_SNP_ID_823371768 m1A Human chr14 - 102008274 102008274 102008274 CAGTGCTTCCTGTATGCACTGCACCTGCTGGGACACAGCCGAGAGCATCCGCTCCTCCAGGCGGT CAGTGCTTCCTGTATGCACTGCACCTGCTGGGGCACAGCCGAGAGCATCCGCTCCTCCAGGCGGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:102008176..102008350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 113725 RMVar_ID_113725 Human_SNP_ID_823372118 m1A Human chr14 + 21360494 21360494 21360494 GGAACAAAGCATGCTTAATATTATTGTACAAAATATCCACTTTGTCTCCTCGAACAGATGTGAAG GGAACAAAGCATGCTTAATATTATTGTACAAACTATCCACTTTGTCTCCTCGAACAGATGTGAAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr14:21358399..21360970 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 113726 RMVar_ID_113726 Human_SNP_ID_823389126 m1A Human chr14 - 100239412 100239412 100239412 TGCCCGTGGCCGCCCCCGCCGCCGTGGTCGCCACCGCCGCCGTCCTCGTCGTCGTCGTCCTCCTC TGCCCGTGGCCGCCCCCGCCGCCGTGGTCGCCGCCGCCGCCGTCCTCGTCGTCGTCGTCCTCCTC T C lnc-DEGS2-3 RNACentral:URS00008C31D7 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr14:100239314..100239468 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113727 RMVar_ID_113727 Human_SNP_ID_823390158 m1A Human chr14 - 100068621 100068621 100068621 ACCACGGCACTTCCTGAATCTGGTGACTTCTCACCGCCTACCCTGACTGCTCCACTGCTGGCCCA ACCACGGCACTTCCTGAATCTGGTGACTTCTCGCCGCCTACCCTGACTGCTCCACTGCTGGCCCA T C AL157912.1 Ensembl:ENSG00000258560 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:100068615..100068780 26863196 MeRIP-seq:(Medium) rs1190964 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,ESCA,frontal_lobe oligodendroglioma_Grade_III 9 brain GWAS_ID_7402 113728 RMVar_ID_113728 Human_SNP_ID_823394030 m1A Human chr14 + 55670757 55670756 55670757 ACAGAGTTATGGTGAATGGTTGCATGGATTTGAAAAAAAGGCAAAAGAATGTATGGCTGGAACTT ACAGAGTTATGGTGAATGGTTGCATGGATTTG_AAAAAAGGCAAAAGAATGTATGGCTGGAACTT GA G KTN1 Ensembl:ENSG00000126777 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA,ICGC 33..33 33 COAD,STAD,UCEC 6 - Human_RBP_ID_4434,Human_RBP_ID_39702,Human_RBP_ID_197017,Human_RBP_ID_1820842,Human_RBP_ID_3453146,Human_RBP_ID_4296474,Human_RBP_ID_5463741,Human_RBP_ID_17187321,Human_RBP_ID_22924088,Human_RBP_ID_23627366,Human_RBP_ID_26325113,Human_RBP_ID_27808332 Human_Splice_Rec_1516876,Human_Splice_Rec_1516877,Human_Splice_Rec_1516976,Human_Splice_Rec_1516977,Human_Splice_Rec_1517062,Human_Splice_Rec_1517063,Human_Splice_Rec_1517150,Human_Splice_Rec_1517151,Human_Splice_Rec_1517232,Human_Splice_Rec_1517233,Human_Splice_Rec_1517312,Human_Splice_Rec_1517313,Human_Splice_Rec_1517392,Human_Splice_Rec_1517393,Human_Splice_Rec_1517470,Human_Splice_Rec_1517471,Human_Splice_Rec_1517532,Human_Splice_Rec_1517533,Human_Splice_Rec_1517544,Human_Splice_Rec_1517545,Human_Splice_Rec_1517564,Human_Splice_Rec_1517565,Human_Splice_Rec_1517582,Human_Splice_Rec_1517583 RMVar_hsa_circ_53501,RMVar_hsa_circ_72947,RMVar_hsa_circ_166840,RMVar_hsa_circ_267966,RMVar_hsa_circ_90011,RMVar_hsa_circ_166846,RMVar_hsa_circ_107042,RMVar_hsa_circ_166848,RMVar_hsa_circ_101205,RMVar_hsa_circ_166850,RMVar_hsa_circ_8884,RMVar_hsa_circ_56816,RMVar_hsa_circ_60279,RMVar_hsa_circ_361777,RMVar_hsa_circ_62590,RMVar_hsa_circ_369013,RMVar_hsa_circ_53956,RMVar_hsa_circ_50311,RMVar_hsa_circ_66178,RMVar_hsa_circ_50242,RMVar_hsa_circ_68784,RMVar_hsa_circ_377270,RMVar_hsa_circ_54020,RMVar_hsa_circ_362543,RMVar_hsa_circ_166857 113729 RMVar_ID_113729 Human_SNP_ID_823408525 m1A Human chr14 - 73719465 73719465 73719465 GTGACATCCTCATCCTCCGGAGCCACGAGTCCAACGCCCCTGGGTCTGCCGGTGGCCAGGCCTCG GTGACATCCTCATCCTCCGGAGCCACGAGTCCGACGCCCCTGGGTCTGCCGGTGGCCAGGCCTCG T C MIDEAS Ensembl:ENSG00000156030 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr14:73719416..73721461 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_758402,Human_RBP_ID_880584,Human_RBP_ID_9369184 Human_Splice_Rec_1534046,Human_Splice_Rec_1534058,Human_Splice_Rec_1534080,Human_Splice_Rec_1534100,Human_Splice_Rec_1534104,Human_Splice_Rec_1534126,Human_Splice_Rec_1534148 RMVar_hsa_circ_545 113730 RMVar_ID_113730 Human_SNP_ID_823419043 m1A Human chr14 - 91293158 91293158 91293158 AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTATGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC AGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGCAGGTGAGGATGGGAAGGTGGGCTGTGGC T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr14:91293123..91293251 26863196 MeRIP-seq:(Medium) rs77218441 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,COCA,central_nervous_system astrocytoma_Grade_III,large_intestine adenocarcinoma 3 large intestine,brain RMVar_hsa_circ_13080,RMVar_hsa_circ_268120,RMVar_hsa_circ_267046,RMVar_hsa_circ_300694,RMVar_hsa_circ_168578,RMVar_hsa_circ_168579,RMVar_hsa_circ_168580,RMVar_hsa_circ_285705 113731 RMVar_ID_113731 Human_SNP_ID_823431128 m1A Human chr14 + 102139978 102139978 102139978 AGGAGATGAACGAGATTAAGACCCAATTCACCACCCGGGAAGGTCTGTACAAGCTGCTGCCGCAC AGGAGATGAACGAGATTAAGACCCAATTCACCGCCCGGGAAGGTCTGTACAAGCTGCTGCCGCAC A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr14:102139933..102140065 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 9 large intestine Human_RBP_ID_1488015,Human_RBP_ID_5463132,Human_RBP_ID_8230421,Human_RBP_ID_9370481,Human_RBP_ID_22183327 Human_Splice_Rec_1556817 113732 RMVar_ID_113732 Human_SNP_ID_823431151 m1A Human chr14 - 23275537 23275537 23275537 GAGCTGGGGGAGGGGAGGTCTGTTACTGAAAGATGAACCAACTTAGTAACTGTTTAAACAAAGAA GAGCTGGGGGAGGGGAGGTCTGTTACTGAAAGGTGAACCAACTTAGTAACTGTTTAAACAAAGAA T C HOMEZ Ensembl:ENSG00000215271 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr14:23275528..23275735 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113733 RMVar_ID_113733 Human_SNP_ID_829831215 m1A Human chr18 + 63318051 63318051 63318051 CTCCAACCCCCGCATCTCGGACCTGTGGCCTCAGCCCAGACTCACATCACCAAGTGCACCTACCC CTCCAACCCCCGCATCTCGGACCTGTGGCCTCGGCCCAGACTCACATCACCAAGTGCACCTACCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:63318001..63318112 26863196 MeRIP-seq:(Medium) rs748213542 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue 113734 RMVar_ID_113734 Human_SNP_ID_829841841 m1A Human chr18 + 8786021 8786021 8786021 GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGAGCTGCACCGCCGCGCAGACGGGGACACCGGGA GCGGGAGAGCCTGCGCCTCCGAGCCGCGCGGGGGCTGCACCGCCGCGCAGACGGGGACACCGGGA A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:8785971..8786060 26863196 MeRIP-seq:(Medium) rs753490941 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_9291053 Human_Splice_Rec_1893042,Human_Splice_Rec_1893043,Human_Splice_Rec_1893068,Human_Splice_Rec_1893069,Human_Splice_Rec_1893098,Human_Splice_Rec_1893099,Human_Splice_Rec_1893136,Human_Splice_Rec_1893137,Human_Splice_Rec_1893162,Human_Splice_Rec_1893163,Human_Splice_Rec_1893174,Human_Splice_Rec_1893176,Human_Splice_Rec_1893177 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_82388,RMVar_hsa_circ_188484,RMVar_hsa_circ_75218,RMVar_hsa_circ_268080,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_265351,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_347398,RMVar_hsa_circ_37579,RMVar_hsa_circ_188489 113735 RMVar_ID_113735 Human_SNP_ID_829849901 m1A Human chr18 - 319935 319935 319935 CTCATCAGATTGAAAAAAAAAAAGCACTGAAAACCAATTACTGAAAAAAAATTGACAGCTAGTGT CTCATCAGATTGAAAAAAAAAAAGCACTGAAAGCCAATTACTGAAAAAAAATTGACAGCTAGTGT T C COLEC12 Ensembl:ENSG00000158270 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12190 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_9079916 113736 RMVar_ID_113736 Human_SNP_ID_829861487 m1A Human chr18 + 11881553 11881553 11881553 CCTGAGCCACGGCCGTCTCTGATTCTCCCTTTATGAAGCTGCAGGCTGACGAGAGATGGTCCCTT CCTGAGCCACGGCCGTCTCTGATTCTCCCTTTGTGAAGCTGCAGGCTGACGAGAGATGGTCCCTT A G GNAL Ensembl:ENSG00000141404 Protein coding 3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:11881458..11881600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 4 uterus Human_RBP_ID_4494728,Human_RBP_ID_27561647 113737 RMVar_ID_113737 Human_SNP_ID_829913111 m1A Human chr18 + 6729426 6729416 6729426 GCGCACACACAGGCACAAACACAGGCGCACACATAGGCGCACACACACACAGGCGTGCACACGTA GCGCACACACAGGCACAAACACA__________TAGGCGCACACACACACAGGCGTGCACACGTA AGGCGCACACA A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:6729389..6729504 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 24..33 33 LMS 1 - 113738 RMVar_ID_113738 Human_SNP_ID_829945203 m1A Human chr18 + 12358782 12358782 12358782 CCTCCTCACAGCCAGCCACATCTTTGAACTTCACATCAATTTCATCCTTTAAGACCTTGGCAGTG CCTCCTCACAGCCAGCCACATCTTTGAACTTCGCATCAATTTCATCCTTTAAGACCTTGGCAGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:12358732..12358878 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder 113739 RMVar_ID_113739 Human_SNP_ID_829950182 m1A Human chr18 - 48730458 48730458 48730458 CCCTCACACCGCGGAAGCCCCTCACACCGCGGAAGCCCCTCACACCACAGGGGCCCCTCACAGCG CCCTCACACCGCGGAAGCCCCTCACACCGCGGGAGCCCCTCACACCACAGGGGCCCCTCACAGCG T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:48729997..48731089 26863196 MeRIP-seq:(Medium) rs1377933784 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 113740 RMVar_ID_113740 Human_SNP_ID_829959254 m1A Human chr18 - 48730352 48730352 48730352 GCCCCTCACACCGCAGGGGCCCCTCACACAGCAGGAGCCCCTCACACCGCAGGGGCCCCTCACAC GCCCCTCACACCGCAGGGGCCCCTCACACAGCGGGAGCCCCTCACACCGCAGGGGCCCCTCACAC T C HSALNG0121448 RNACentral:URS0000EA7202 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:48730023..48731016 26863196 MeRIP-seq:(Medium) rs986792490 Functional Loss SNV ICGC 33..33 33 MALY 1 - 113741 RMVar_ID_113741 Human_SNP_ID_829984827 m1A Human chr18 + 3256114 3256114 3256114 CTATTAATATCATTTTCAGAATAAAAAATAGGATAATTTAACCTACCAGCCCTTCTCCCCCAATA CTATTAATATCATTTTCAGAATAAAAAATAGGGTAATTTAACCTACCAGCCCTTCTCCCCCAATA A G MYL12A Ensembl:ENSG00000101608 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7811 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_507303,Human_RBP_ID_1370915,Human_RBP_ID_6681787,Human_RBP_ID_17265030,Human_RBP_ID_17381577,Human_RBP_ID_17496148,Human_RBP_ID_17655238,Human_RBP_ID_17908838,Human_RBP_ID_18298969,Human_RBP_ID_22390441,Human_RBP_ID_24417777,Human_RBP_ID_24483257,Human_RBP_ID_26978640,Human_RBP_ID_27461070 Human_miRNA_ID_966995 GWAS_ID_8306,GWAS_ID_8307,GWAS_ID_8308,GWAS_ID_8309,GWAS_ID_8310,GWAS_ID_8311,GWAS_ID_8312,GWAS_ID_8313,GWAS_ID_8314,GWAS_ID_8315,GWAS_ID_8316,GWAS_ID_8317,GWAS_ID_8318,GWAS_ID_8319,GWAS_ID_8320,GWAS_ID_8321,GWAS_ID_8322,GWAS_ID_8323,GWAS_ID_8324,GWAS_ID_8325,GWAS_ID_8326,GWAS_ID_8327,GWAS_ID_8328,GWAS_ID_8329,GWAS_ID_8330,GWAS_ID_8331,GWAS_ID_8332 RMVar_hsa_circ_126747,RMVar_hsa_circ_111475,RMVar_hsa_circ_188309,RMVar_hsa_circ_188310,RMVar_hsa_circ_188311 113742 RMVar_ID_113742 Human_SNP_ID_829991723 m1A Human chr18 + 8796283 8796283 8796283 ATGCCTTGAGGTGGAAAGAACTGGAAATGCACAGCCTGGCTTTGCAAAACACCCTCCATGAGCGA ATGCCTTGAGGTGGAAAGAACTGGAAATGCACGGCCTGGCTTTGCAAAACACCCTCCATGAGCGA A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8796195..8796313 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_905467 Human_Splice_Rec_1893044,Human_Splice_Rec_1893070,Human_Splice_Rec_1893102,Human_Splice_Rec_1893140,Human_Splice_Rec_1893164,Human_Splice_Rec_1893180 RMVar_hsa_circ_17313,RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_75218,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486,RMVar_hsa_circ_337402,RMVar_hsa_circ_350064,RMVar_hsa_circ_352467,RMVar_hsa_circ_39604,RMVar_hsa_circ_293657,RMVar_hsa_circ_188488,RMVar_hsa_circ_37579,RMVar_hsa_circ_295583,RMVar_hsa_circ_188489,RMVar_hsa_circ_46534,RMVar_hsa_circ_17490 113743 RMVar_ID_113743 Human_SNP_ID_830013824 m1A Human chr18 - 23201839 23201835 23201839 GGTCTCCCCATTGCCCCAGAGTGTCCTTCCCCAACCCTGGCTGCCTCAGTCTCTCTCCATGGCAC GGTCTCCCCATTGCCCCAGAGTGTCCTTCCCC____CTGGCTGCCTCAGTCTCTCTCCATGGCAC GGGTT G TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23201836..23202176 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..36 33 OV 1 - 113744 RMVar_ID_113744 Human_SNP_ID_830022792 m1A Human chr18 + 8706285 8706285 8706285 CCCGCTGCTCGCGCATCAGCCACACGGACAGCAGCTCCGACCTCTCTGACTGCCCCTCCGAACCC CCCGCTGCTCGCGCATCAGCCACACGGACAGCGGCTCCGACCTCTCTGACTGCCCCTCCGAACCC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr18:8706197..8706354 26863196 MeRIP-seq:(Medium) rs1320347690 Functional Loss SNV ICGC 33..33 33 THCA 1 - 113745 RMVar_ID_113745 Human_SNP_ID_830085676 m1A Human chr18 - 54271297 54271289 54271298 TTCAGGCTGCTTATTATCTCTGAGCAACTGACAGTTCCTTAAAACATGGTACCTGTGAAGGAAGA TTCAGGCTGCTTATTATCTCTGAGCAACTGA_________AAAACATGGTACCTGTGAAGGAAGA TAAGGAACTG T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:54271296..54271400 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..40 33 KIRC 1 - 113746 RMVar_ID_113746 Human_SNP_ID_830095388 m1A Human chr18 - 57602386 57602386 57602386 AATACTGGCAGGTTATAAAAGGGAAGGGATTGACCCCACTCCCTATTACTGGTATACGGATCAGG AATACTGGCAGGTTATAAAAGGGAAGGGATTGGCCCCACTCCCTATTACTGGTATACGGATCAGG T C NARS1 Ensembl:ENSG00000134440 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:57601752..57602473 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1371348,Human_RBP_ID_1550924,Human_RBP_ID_4496266,Human_RBP_ID_5144696,Human_RBP_ID_8827768,Human_RBP_ID_9291001,Human_RBP_ID_9379892,Human_RBP_ID_17381299,Human_RBP_ID_17911222,Human_RBP_ID_18993748,Human_RBP_ID_22445904,Human_RBP_ID_22501276,Human_RBP_ID_22762378,Human_RBP_ID_27673227 Human_Splice_Rec_1917797,Human_Splice_Rec_1917801,Human_Splice_Rec_1917823 RMVar_hsa_circ_190322,RMVar_hsa_circ_118035,RMVar_hsa_circ_120281,RMVar_hsa_circ_121799,RMVar_hsa_circ_119396,RMVar_hsa_circ_110138,RMVar_hsa_circ_114273,RMVar_hsa_circ_190324,RMVar_hsa_circ_190325,RMVar_hsa_circ_190323,RMVar_hsa_circ_190320,RMVar_hsa_circ_190321 113747 RMVar_ID_113747 Human_SNP_ID_830159008 m1A Human chr18 - 75209225 75209225 75209225 GGGGGCTGCGCCGGCGCCGGGGAGGCGGGGGGAGCGGGAGCGGGCGACGCGGGGAAGGGGGGAGC GGGGGCTGCGCCGGCGCCGGGGAGGCGGGGGGGGCGGGAGCGGGCGACGCGGGGAAGGGGGGAGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:75209148..75209249 26863410 MeRIP-seq:(Medium) rs902122845 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5189538,Human_RBP_ID_26783276 113748 RMVar_ID_113748 Human_SNP_ID_830167562 m1A Human chr18 - 21111688 21111688 21111688 CCGCGACTCGCCCTTTCCCCGGCTGGGACCGCAGCCCCTCCCAGAAGCTCCCCCATCAGCAGCCG CCGCGACTCGCCCTTTCCCCGGCTGGGACCGCGGCCCCTCCCAGAAGCTCCCCCATCAGCAGCCG T C ROCK1 Ensembl:ENSG00000067900 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr18:21111547..21111775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_4494159 113749 RMVar_ID_113749 Human_SNP_ID_830185209 m1A Human chr18 + 36138363 36138363 36138363 ACCAGAGGAGGACATCAGATCCTGCATTATGTACACTGATCGTTTCTGCAGCTGCAGATTCTGCT ACCAGAGGAGGACATCAGATCCTGCATTATGTCCACTGATCGTTTCTGCAGCTGCAGATTCTGCT A C ELP2 Ensembl:ENSG00000134759 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1785934 Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,COCA,mouth squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 26 pancreas,head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_905511,Human_RBP_ID_5189222,Human_RBP_ID_18716537,Human_RBP_ID_18993660,Human_RBP_ID_22445880,Human_RBP_ID_22965668 Human_Splice_Rec_1905720,Human_Splice_Rec_1905721,Human_Splice_Rec_1905730,Human_Splice_Rec_1905731,Human_Splice_Rec_1905740,Human_Splice_Rec_1905741,Human_Splice_Rec_1905782,Human_Splice_Rec_1905783,Human_Splice_Rec_1905794,Human_Splice_Rec_1905795,Human_Splice_Rec_1905838,Human_Splice_Rec_1905839,Human_Splice_Rec_1905874,Human_Splice_Rec_1905875,Human_Splice_Rec_1905916,Human_Splice_Rec_1905917,Human_Splice_Rec_1905958,Human_Splice_Rec_1905964,Human_Splice_Rec_1905965,Human_Splice_Rec_1905972,Human_Splice_Rec_1905973,Human_Splice_Rec_1905984,Human_Splice_Rec_1905985,Human_Splice_Rec_1906024,Human_Splice_Rec_1906025,Human_Splice_Rec_1906066,Human_Splice_Rec_1906067,Human_Splice_Rec_1906076,Human_Splice_Rec_1906077,Human_Splice_Rec_1906085 Human_miRNA_ID_2730250,Human_miRNA_ID_2769326 GWAS_ID_7878,GWAS_ID_7879,GWAS_ID_7880 RMVar_hsa_circ_2640,RMVar_hsa_circ_109972,RMVar_hsa_circ_334505,RMVar_hsa_circ_340301,RMVar_hsa_circ_368254,RMVar_hsa_circ_39164,RMVar_hsa_circ_189644,RMVar_hsa_circ_189645,RMVar_hsa_circ_189646,RMVar_hsa_circ_40813,RMVar_hsa_circ_189647 113750 RMVar_ID_113750 Human_SNP_ID_830202536 m1A Human chr18 + 12703068 12703068 12703068 GCTTCCGCCTTCTTGCTGCCCTCGTTCTTGCCAGGGCCGCGGTTAGTCCCTGCTGGCCACCCCAC GCTTCCGCCTTCTTGCTGCCCTCGTTCTTGCCGGGGCCGCGGTTAGTCCCTGCTGGCCACCCCAC A G PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:12703026..12703150 26863196 MeRIP-seq:(Medium) rs3809916 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4482729,Human_RBP_ID_5319528,Human_RBP_ID_9327722,Human_RBP_ID_17381596,Human_RBP_ID_17497563 Human_Splice_Rec_1896109,Human_Splice_Rec_1896119,Human_Splice_Rec_1896127 Human_miRNA_ID_2346517 GWAS_ID_8348,GWAS_ID_8349,GWAS_ID_8350,GWAS_ID_8351,GWAS_ID_8352,GWAS_ID_8353,GWAS_ID_8354,GWAS_ID_8355,GWAS_ID_8356,GWAS_ID_8357,GWAS_ID_8358,GWAS_ID_8359,GWAS_ID_8360,GWAS_ID_8361,GWAS_ID_8362,GWAS_ID_8363,GWAS_ID_8364,GWAS_ID_8365,GWAS_ID_8366,GWAS_ID_8367,GWAS_ID_8368,GWAS_ID_8369,GWAS_ID_8370,GWAS_ID_8371,GWAS_ID_8372,GWAS_ID_8373,GWAS_ID_8374,GWAS_ID_8375,GWAS_ID_8376,GWAS_ID_8377,GWAS_ID_8378 RMVar_hsa_circ_78226,RMVar_hsa_circ_188748,RMVar_hsa_circ_101036,RMVar_hsa_circ_188758 113751 RMVar_ID_113751 Human_SNP_ID_830260098 m1A Human chr18 - 7629893 7629893 7629893 TCATTCACCTGGAATACTTCAATAGTCTATTAACCAGTCCACTGCCACCCACTCTACCTCCTCCA TCATTCACCTGGAATACTTCAATAGTCTATTACCCAGTCCACTGCCACCCACTCTACCTCCTCCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:7629887..7630287 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113752 RMVar_ID_113752 Human_SNP_ID_830290635 m1A Human chr18 - 12610027 12610025 12610028 GGGTGGGGAGGAAGCATCAGTGAGGAGCAAGAAGGACCTCCTCCCAGTTCCAGGTTCAGCAACCT GGGTGGGGAGGAAGCATCAGTGAGGAGCAAG___GACCTCCTCCCAGTTCCAGGTTCAGCAACCT CCTT C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12610022..12610456 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 NKTL 1 - RMVar_hsa_circ_27694,RMVar_hsa_circ_39094,RMVar_hsa_circ_323244,RMVar_hsa_circ_25748,RMVar_hsa_circ_188745,RMVar_hsa_circ_293988,RMVar_hsa_circ_329291,RMVar_hsa_circ_188747 113753 RMVar_ID_113753 Human_SNP_ID_830320334 m1A Human chr18 - 12279524 12279524 12279524 TTCTGAATGTCCTCCCCTTTCCCATGGGGAGAAGGCCAGCCCGTCCCTTCCCCAATTCCTCCCTT TTCTGAATGTCCTCCCCTTTCCCATGGGGAGACGGCCAGCCCGTCCCTTCCCCAATTCCTCCCTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:12279478..12279561 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113754 RMVar_ID_113754 Human_SNP_ID_830331668 m1A Human chr18 - 47896667 47896667 47896667 AAGTCAGCTGGTGGGTCTGGAGGAGCAGGCGGAGGAGAGCAGAATGGGCAGGAAGAAAAGTGGTG AAGTCAGCTGGTGGGTCTGGAGGAGCAGGCGGTGGAGAGCAGAATGGGCAGGAAGAAAAGTGGTG T A SMAD2 Ensembl:ENSG00000175387 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr18:47896576..47896700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_52131,Human_RBP_ID_823162,Human_RBP_ID_906226,Human_RBP_ID_3953578,Human_RBP_ID_6690175,Human_RBP_ID_9379607 RMVar_hsa_circ_189979,RMVar_hsa_circ_267989,RMVar_hsa_circ_189985,RMVar_hsa_circ_189982,RMVar_hsa_circ_189983,RMVar_hsa_circ_328037,RMVar_hsa_circ_189986,RMVar_hsa_circ_374009,RMVar_hsa_circ_189992,RMVar_hsa_circ_289782,RMVar_hsa_circ_189995,RMVar_hsa_circ_277105,RMVar_hsa_circ_189996,RMVar_hsa_circ_315585,RMVar_hsa_circ_111810,RMVar_hsa_circ_190003,RMVar_hsa_circ_375058,RMVar_hsa_circ_190004,RMVar_hsa_circ_63495,RMVar_hsa_circ_104260,RMVar_hsa_circ_190005,RMVar_hsa_circ_190006,RMVar_hsa_circ_321247,RMVar_hsa_circ_60536 113755 RMVar_ID_113755 Human_SNP_ID_830356983 m1A Human chr18 - 35497894 35497894 35497894 AAGGCCCGCGCTGGGAAAAAGGTGGGGGGACCAGGGGAAGACTCGGAGTGCGATGGCGGCGCAAA AAGGCCCGCGCTGGGAAAAAGGTGGGGGGACCTGGGGAAGACTCGGAGTGCGATGGCGGCGCAAA T A AC007998.2,INO80C Ensembl:ENSG00000267140,Ensembl:ENSG00000153391 Protein coding,Protein coding 5'UTR,5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr18:35497692..35497993;chr18:35446949..35497988;chr18:35446949..35498000;chr18:35497780..35497996 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 7 liver Human_RBP_ID_507727,Human_RBP_ID_4486671,Human_RBP_ID_18420720 113756 RMVar_ID_113756 Human_SNP_ID_830371676 m1A Human chr18 - 5419772 5419755 5419772 GAAGAAGGCTGAGGAGGAGCGGGACGAGGAAGAGGACAAACGGAGGAAGGGGGAAGAAGTCACGC GAAGAAGGCTGAGGAGGAGCGGGACGAGGAAG_________________GGGGAAGAAGTCACGC CCTTCCTCCGTTTGTCCT C EPB41L3 Ensembl:ENSG00000082397 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:5419681..5419780 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..49 33 BRCA 1 - Human_RBP_ID_22964553,Human_RBP_ID_26980075 Human_Splice_Rec_1891029,Human_Splice_Rec_1891069,Human_Splice_Rec_1891111,Human_Splice_Rec_1891155,Human_Splice_Rec_1891185,Human_Splice_Rec_1891231,Human_Splice_Rec_1891273,Human_Splice_Rec_1891313,Human_Splice_Rec_1891333,Human_Splice_Rec_1891343,Human_Splice_Rec_1891349,Human_Splice_Rec_1891359,Human_Splice_Rec_1891369,Human_Splice_Rec_1891381,Human_Splice_Rec_1891389,Human_Splice_Rec_1891405 Human_miRNA_ID_2255586,Human_miRNA_ID_2571306,Human_miRNA_ID_3045043 RMVar_hsa_circ_67717,RMVar_hsa_circ_345863,RMVar_hsa_circ_58303,RMVar_hsa_circ_93422,RMVar_hsa_circ_188342,RMVar_hsa_circ_188343,RMVar_hsa_circ_27828,RMVar_hsa_circ_363187,RMVar_hsa_circ_272767,RMVar_hsa_circ_316415,RMVar_hsa_circ_272037,RMVar_hsa_circ_188348,RMVar_hsa_circ_188349,RMVar_hsa_circ_188347,RMVar_hsa_circ_54766,RMVar_hsa_circ_65324 113757 RMVar_ID_113757 Human_SNP_ID_830389472 m1A Human chr18 + 7629888 7629888 7629888 GTTCATGGAGGAGGTAGAGTGGGTGGCAGTGGACTGGTTAATAGACTATTGAAGTATTCCAGGTG GTTCATGGAGGAGGTAGAGTGGGTGGCAGTGGGCTGGTTAATAGACTATTGAAGTATTCCAGGTG A G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:7629885..7630339 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113758 RMVar_ID_113758 Human_SNP_ID_830430581 m1A Human chr18 - 756769 756769 756769 CAAAAGTCCAGCCATTAAATACAGACCTGAAAATACTCCAGAGCCTGTCAGTACAAGTGTGAGCC CAAAAGTCCAGCCATTAAATACAGACCTGAAAGTACTCCAGAGCCTGTCAGTACAAGTGTGAGCC T C YES1 Ensembl:ENSG00000176105 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:756718..756792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_8095203,Human_RBP_ID_8828443,Human_RBP_ID_23778198,Human_RBP_ID_27673953 Human_Splice_Rec_1888342,Human_Splice_Rec_1888364,Human_Splice_Rec_1888386,Human_Splice_Rec_1888410,Human_Splice_Rec_1888416 Human_miRNA_ID_2735683,Human_miRNA_ID_2793671,Human_miRNA_ID_3070009 RMVar_hsa_circ_37324,RMVar_hsa_circ_188211,RMVar_hsa_circ_326286,RMVar_hsa_circ_188213,RMVar_hsa_circ_359835,RMVar_hsa_circ_188214,RMVar_hsa_circ_54908,RMVar_hsa_circ_324219,RMVar_hsa_circ_277591,RMVar_hsa_circ_188222,RMVar_hsa_circ_9263,RMVar_hsa_circ_368176,RMVar_hsa_circ_271521,RMVar_hsa_circ_365129,RMVar_hsa_circ_188223 113759 RMVar_ID_113759 Human_SNP_ID_830464406 m1A Human chr18 + 23919951 23919951 23919951 GGCTAAAAATGTTGTGGCTGAGACTAGGTGGGATGACATAAAGAGAGAGCTAAGAATGGCAGAAT GGCTAAAAATGTTGTGGCTGAGACTAGGTGGGGTGACATAAAGAGAGAGCTAAGAATGGCAGAAT A G LAMA3 Ensembl:ENSG00000053747 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:23919900..23920013 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_87137,RMVar_hsa_circ_112354,RMVar_hsa_circ_189186,RMVar_hsa_circ_189188,RMVar_hsa_circ_89391,RMVar_hsa_circ_113895,RMVar_hsa_circ_92369,RMVar_hsa_circ_111716,RMVar_hsa_circ_189191,RMVar_hsa_circ_189193,RMVar_hsa_circ_90386,RMVar_hsa_circ_189192,RMVar_hsa_circ_124745,RMVar_hsa_circ_119388,RMVar_hsa_circ_114666,RMVar_hsa_circ_94995,RMVar_hsa_circ_100508,RMVar_hsa_circ_96786,RMVar_hsa_circ_91103,RMVar_hsa_circ_125940,RMVar_hsa_circ_189215,RMVar_hsa_circ_189216,RMVar_hsa_circ_189211,RMVar_hsa_circ_189213,RMVar_hsa_circ_189214,RMVar_hsa_circ_189212,RMVar_hsa_circ_189209,RMVar_hsa_circ_189210,RMVar_hsa_circ_189208,RMVar_hsa_circ_13370,RMVar_hsa_circ_26771,RMVar_hsa_circ_189227,RMVar_hsa_circ_337698,RMVar_hsa_circ_16919,RMVar_hsa_circ_189234,RMVar_hsa_circ_22172,RMVar_hsa_circ_78857,RMVar_hsa_circ_372269,RMVar_hsa_circ_189236,RMVar_hsa_circ_116907,RMVar_hsa_circ_189237,RMVar_hsa_circ_189239 113760 RMVar_ID_113760 Human_SNP_ID_830491212 m1A Human chr18 + 54224229 54224229 54224229 GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCAGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC GGCGCCGCCGCCACCGCTGCCGCCGCCGCCGCCGCCGCCGCCGTCGCCGCCAAGGCCGCTGCCGC A C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr18:54224136..54224490 26863410 MeRIP-seq:(Medium) rs530077528 Functional Loss SNV ICGC 33..33 33 BOCA 1 - 113761 RMVar_ID_113761 Human_SNP_ID_830514322 m1A Human chr18 - 48951512 48951512 48951512 CTGTCAGCCCCGCCGGGCTCAGCCGCCGCCGCAGCATCTTCTGCCCCTGCGCCCGCGCCAGCCTC CTGTCAGCCCCGCCGGGCTCAGCCGCCGCCGCCGCATCTTCTGCCCCTGCGCCCGCGCCAGCCTC T G SMAD7 Ensembl:ENSG00000101665 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr18:48951424..48951521 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4488197 113762 RMVar_ID_113762 Human_SNP_ID_830519786 m1A Human chr18 + 54378271 54378271 54378271 AAATGTGAAGAGGAAAATGAAACTGTCACCACAATGAATAGTCACCACAGAACAAATAGGCATTT AAATGTGAAGAGGAAAATGAAACTGTCACCACGATGAATAGTCACCACAGAACAAATAGGCATTT A G C18orf54 Ensembl:ENSG00000166845 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3753056 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_27814611 Human_Splice_Rec_1914550,Human_Splice_Rec_1914560,Human_Splice_Rec_1914572,Human_Splice_Rec_1914586,Human_Splice_Rec_1914600,Human_Splice_Rec_1914608,Human_Splice_Rec_1914610,Human_Splice_Rec_1914611 GWAS_ID_11867,GWAS_ID_11868,GWAS_ID_11869,GWAS_ID_11870,GWAS_ID_11871,GWAS_ID_11872,GWAS_ID_11873,GWAS_ID_11874,GWAS_ID_11875,GWAS_ID_11876,GWAS_ID_11877,GWAS_ID_11878,GWAS_ID_11879,GWAS_ID_11880,GWAS_ID_11881,GWAS_ID_11882,GWAS_ID_11883,GWAS_ID_11884,GWAS_ID_11885,GWAS_ID_11886,GWAS_ID_11887,GWAS_ID_11888,GWAS_ID_11889,GWAS_ID_11890,GWAS_ID_11891,GWAS_ID_11892,GWAS_ID_11893,GWAS_ID_11894,GWAS_ID_11895,GWAS_ID_11896,GWAS_ID_11897,GWAS_ID_11898,GWAS_ID_11899,GWAS_ID_11900,GWAS_ID_11901,GWAS_ID_11902,GWAS_ID_11903,GWAS_ID_11904,GWAS_ID_11905,GWAS_ID_11906,GWAS_ID_11907,GWAS_ID_11908,GWAS_ID_11909,GWAS_ID_11910,GWAS_ID_11911,GWAS_ID_11912,GWAS_ID_11913,GWAS_ID_11914,GWAS_ID_11915,GWAS_ID_11916,GWAS_ID_11917,GWAS_ID_11918,GWAS_ID_11919,GWAS_ID_11920,GWAS_ID_11921,GWAS_ID_11922,GWAS_ID_11923,GWAS_ID_11924,GWAS_ID_11925,GWAS_ID_11926,GWAS_ID_11927,GWAS_ID_11928,GWAS_ID_11929,GWAS_ID_11930,GWAS_ID_11931,GWAS_ID_11932,GWAS_ID_11933,GWAS_ID_11934,GWAS_ID_11935,GWAS_ID_11936,GWAS_ID_11937,GWAS_ID_11938,GWAS_ID_11939,GWAS_ID_11940,GWAS_ID_11941,GWAS_ID_11942,GWAS_ID_11943,GWAS_ID_11944,GWAS_ID_11945,GWAS_ID_11946,GWAS_ID_11947,GWAS_ID_11948,GWAS_ID_11949,GWAS_ID_11950,GWAS_ID_11951,GWAS_ID_11952,GWAS_ID_11953,GWAS_ID_11954,GWAS_ID_11955,GWAS_ID_11956,GWAS_ID_11957,GWAS_ID_11958,GWAS_ID_11959,GWAS_ID_11960,GWAS_ID_11961,GWAS_ID_11962,GWAS_ID_11963,GWAS_ID_11964,GWAS_ID_11965,GWAS_ID_11966,GWAS_ID_11967,GWAS_ID_11968,GWAS_ID_11969,GWAS_ID_11970,GWAS_ID_11971,GWAS_ID_11972,GWAS_ID_11973,GWAS_ID_11974,GWAS_ID_11975,GWAS_ID_11976,GWAS_ID_11977,GWAS_ID_11978,GWAS_ID_11979 113763 RMVar_ID_113763 Human_SNP_ID_830535412 m1A Human chr18 - 23296522 23296522 23296522 AAGCAGATCACCTGAGGTCGGGAGTTCAAGACAAACCTGGCCAACATGGTGAAACCCTGTCTCTA AAGCAGATCACCTGAGGTCGGGAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCTGTCTCTA T G TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9954334 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_7898,GWAS_ID_7899,GWAS_ID_7900,GWAS_ID_7901,GWAS_ID_7902,GWAS_ID_7903,GWAS_ID_7904 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102 113764 RMVar_ID_113764 Human_SNP_ID_830617631 m1A Human chr18 + 50106003 50106003 50106003 AGTCACCCTCTCCAGCTACTTTTTATAGAACCACCTCAAATTCATACTATTCAAGCCATAACTCA AGTCACCCTCTCCAGCTACTTTTTATAGAACCCCCTCAAATTCATACTATTCAAGCCATAACTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:50106001..50106251 26863196 MeRIP-seq:(Medium) rs992784480 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113765 RMVar_ID_113765 Human_SNP_ID_830724426 m1A Human chr18 + 39800232 39800232 39800232 GGCAGGGTTTTATTGGGTAAAAAGGGGAAAAAAGGGGGGACACAGGTATTCCCTCACAAGGTCAG GGCAGGGTTTTATTGGGTAAAAAGGGGAAAAAGGGGGGGACACAGGTATTCCCTCACAAGGTCAG A G lnc-PIK3C3-11 RNACentral:URS00008B795F lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:39800186..39800260 26863196 MeRIP-seq:(Medium) rs1568141390 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 113766 RMVar_ID_113766 Human_SNP_ID_830811585 m1A Human chr18 + 79753701 79753701 79753701 TGAATGAAGAGGACGCCGCCAGCGAGTCCAGCAGGGAGTCCAGCAACGAGGATGAGGGCAGCAGC TGAATGAAGAGGACGCCGCCAGCGAGTCCAGCTGGGAGTCCAGCAACGAGGATGAGGGCAGCAGC A T CTDP1 Ensembl:ENSG00000060069 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:79753602..79753745 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 6 lung Human_Splice_Rec_1927418,Human_Splice_Rec_1927440,Human_Splice_Rec_1927462,Human_Splice_Rec_1927494,Human_Splice_Rec_1927500 Human_miRNA_ID_1093864 113767 RMVar_ID_113767 Human_SNP_ID_830846405 m1A Human chr18 + 58550370 58550370 58550370 ATCATGAACAACCCCATCTCTGTCTCTATCACATACAACCCCATCCCCATCTCCATCACCTACAA ATCATGAACAACCCCATCTCTGTCTCTATCACCTACAACCCCATCCCCATCTCCATCACCTACAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:58550197..58550406 26863196 MeRIP-seq:(Medium) rs111768148 Functional Loss SNV ICGC 33..33 33 MELA 1 - 113768 RMVar_ID_113768 Human_SNP_ID_830861244 m1A Human chr18 - 10526140 10526140 10526140 AGGTTCTCACTCACTATTTCTCTGCTTTGGCGAGGTGTTCCAGCCCCTCGTTTATCTTCTGAGCC AGGTTCTCACTCACTATTTCTCTGCTTTGGCGGGGTGTTCCAGCCCCTCGTTTATCTTCTGAGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:10526093..10526211 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113769 RMVar_ID_113769 Human_SNP_ID_830897884 m1A Human chr18 + 11981565 11981565 11981565 GACGGGCGGCGGACTAGGCACAGAGCTGCGGGAGCAGGCACAGGGAGTGTGGAGCCTGGCGGCGG GACGGGCGGCGGACTAGGCACAGAGCTGCGGGGGCAGGCACAGGGAGTGTGGAGCCTGGCGGCGG A G IMPA2 Ensembl:ENSG00000141401 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:11981433..11981794;chr18:11981485..11981663;chr18:11981450..11981814;chr18:11981451..11981818;chr18:11981451..11981816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_769234,Human_RBP_ID_4494327,Human_RBP_ID_5526563 113770 RMVar_ID_113770 Human_SNP_ID_830902009 m1A Human chr18 + 48730696 48730696 48730696 GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGAGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT GTGAGGGGCTTCTGCGGTGTGAGGAGCCCCTGTGGTGTGAGGGGCTTCCGCGGTGTGAGGGGCTT A T CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48730669..48730812 26863196 MeRIP-seq:(Medium) rs73956012 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_65344,RMVar_hsa_circ_126697,RMVar_hsa_circ_70452,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_352374,RMVar_hsa_circ_190023 113771 RMVar_ID_113771 Human_SNP_ID_830964513 m1A Human chr18 + 7037726 7037726 7037726 ACGGGATCTTCCTGGGACTGATCAAGTCGGTGACCAGCCACCCGGACATACTGTTTACCTTAAAA ACGGGATCTTCCTGGGACTGATCAAGTCGGTGTCCAGCCACCCGGACATACTGTTTACCTTAAAA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:7037675..7037752 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113772 RMVar_ID_113772 Human_SNP_ID_830979018 m1A Human chr18 + 48787306 48787306 48787306 AAGGAAAAGAAAGAAGGGAAGGGGAGGCGGGGAAAGGGAAGGAAGAAAGAAAGACAGAAAGAGAG AAGGAAAAGAAAGAAGGGAAGGGGAGGCGGGGGAAGGGAAGGAAGAAAGAAAGACAGAAAGAGAG A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:48787302..48787436 26863196 MeRIP-seq:(Medium) rs957767106 Functional Loss SNV ICGC 33..33 33 SKCA 2 - RMVar_hsa_circ_123550,RMVar_hsa_circ_110483,RMVar_hsa_circ_126697,RMVar_hsa_circ_190014,RMVar_hsa_circ_190015,RMVar_hsa_circ_347133,RMVar_hsa_circ_190025,RMVar_hsa_circ_190023,RMVar_hsa_circ_311144,RMVar_hsa_circ_370888,RMVar_hsa_circ_190026,RMVar_hsa_circ_190028,RMVar_hsa_circ_299318 113773 RMVar_ID_113773 Human_SNP_ID_830983426 m1A Human chr18 + 36067491 36067491 36067491 TTTCGCCGCCCTAGCTGCGGCCTCGCCCCCTCACCCCACCCTTCCCCACGCTCTCACCACGGCCG TTTCGCCGCCCTAGCTGCGGCCTCGCCCCCTCCCCCCACCCTTCCCCACGCTCTCACCACGGCCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr18:36067351..36067550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113774 RMVar_ID_113774 Human_SNP_ID_831017634 m1A Human chr18 - 667577 667577 667577 TCACCATCACCATCACCATCACCATCACCATCACCATCTCCATCACCATCACCATCTCCATCACC TCACCATCACCATCACCATCACCATCACCATCTCCATCTCCATCACCATCACCATCTCCATCACC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:667575..667683 26863196 MeRIP-seq:(Medium) rs371737383 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 113775 RMVar_ID_113775 Human_SNP_ID_831081202 m1A Human chr18 - 76844273 76844273 76844273 CCAAATTGCTACCGCTTTAGGTCATCTCTACCACCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT CCAAATTGCTACCGCTTTAGGTCATCTCTACCCCCCTTTCTCTACTTTTCCTTTTTTTTTTTTTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:76844265..76844501 26863196 MeRIP-seq:(Medium) rs960951204 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113776 RMVar_ID_113776 Human_SNP_ID_831122695 m1A Human chr18 - 63970180 63970180 63970180 CCTCCGTGCCTGCCCCGCCCGGTACCTGGCAGAGGCCCCCACCTCCTGCTGCTGCTGCTGCTGCC CCTCCGTGCCTGCCCCGCCCGGTACCTGGCAGGGGCCCCCACCTCCTGCTGCTGCTGCTGCTGCC T C AC009802.1 Ensembl:ENSG00000283667 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:63970142..63970309 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 113777 RMVar_ID_113777 Human_SNP_ID_831125245 m1A Human chr18 + 51197371 51197349 51197371 ATGGCGGCGGCGGCGGCCGGGTCAGGCGCGGCAGGCGGCGAGCCCCATGGCGGACAGGGCCAGGG ATGGCGGCGGC______________________GGCGGCGAGCCCCATGGCGGACAGGGCCAGGG CGGCGGCCGGGTCAGGCGCGGCA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:51197325..51197506 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 12..33 33 PRAD 1 - 113778 RMVar_ID_113778 Human_SNP_ID_831165909 m1A Human chr18 - 44953199 44953199 44953199 CCCACTCACGTCACTGTCCCACTTGTCATTCGAAGGGTTCATTTCACTGAACACGTCCAGGTTCT CCCACTCACGTCACTGTCCCACTTGTCATTCGGAGGGTTCATTTCACTGAACACGTCCAGGTTCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:44953150..44953244 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113779 RMVar_ID_113779 Human_SNP_ID_831174243 m1A Human chr18 - 46917375 46917375 46917375 TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCAGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG TCGTTGGCGGCAGCGGGAGTGGGTGCGGCGGCGGCGGCGGCGGCGCCCGCGGGTGGTATAAAATG T C PIAS2 Ensembl:ENSG00000078043 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr18:46917322..46917440;chr18:46917326..46917475 26863196 MeRIP-seq:(Medium) rs978866399 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_822967,Human_RBP_ID_4494008,Human_RBP_ID_9327871 Human_Splice_Rec_1910413,Human_Splice_Rec_1910439,Human_Splice_Rec_1910463,Human_Splice_Rec_1910487,Human_Splice_Rec_1910531,Human_Splice_Rec_1910595,Human_Splice_Rec_1910601 RMVar_hsa_circ_88083,RMVar_hsa_circ_189935 113780 RMVar_ID_113780 Human_SNP_ID_831252317 m1A Human chr18 - 47176277 47176277 47176277 TCGCTTGGACTTCGGGGCGGCCTCGGACGGCCATGGCCTTTACCCTGTACTCACTGCTGCAGGCA TCGCTTGGACTTCGGGGCGGCCTCGGACGGCCGTGGCCTTTACCCTGTACTCACTGCTGCAGGCA T C AC012254.2,IER3IP1 Ensembl:ENSG00000267228,Ensembl:ENSG00000134049 Protein coding,Protein coding start codon,start codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:47157497..47176354 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_508915,Human_RBP_ID_1012009,Human_RBP_ID_1290865,Human_RBP_ID_1550153,Human_RBP_ID_4487893,Human_RBP_ID_5238104,Human_RBP_ID_5319609,Human_RBP_ID_5467936,Human_RBP_ID_8471935,Human_RBP_ID_9081289,Human_RBP_ID_9327766,Human_RBP_ID_9379867,Human_RBP_ID_22445974,Human_RBP_ID_22965674 Human_Splice_Rec_1910805,Human_Splice_Rec_1910815,Human_Splice_Rec_1910819,Human_Splice_Rec_1910827,Human_Splice_Rec_1910831 113781 RMVar_ID_113781 Human_SNP_ID_831288074 m1A Human chr18 + 79729068 79729068 79729068 TTGTAAGGAGGATTTAGAGAGTATGGACAAAGAGGTGAGCCAACCCCACGCCCCGGTGCCCGCGC TTGTAAGGAGGATTTAGAGAGTATGGACAAAGCGGTGAGCCAACCCCACGCCCCGGTGCCCGCGC A C CTDP1 Ensembl:ENSG00000060069 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:79729034..79735675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_13340082 Human_Splice_Rec_1927415,Human_Splice_Rec_1927461,Human_Splice_Rec_1927491 RMVar_hsa_circ_190810,RMVar_hsa_circ_342960,RMVar_hsa_circ_308953,RMVar_hsa_circ_288836,RMVar_hsa_circ_190809,RMVar_hsa_circ_190811 113782 RMVar_ID_113782 Human_SNP_ID_831347580 m1A Human chr18 + 24018549 24018549 24018549 GCAATGTAGGTGTAGGTAAAGCTGATGGTGATAGGGAGGCTGGGAGACATACGCATGGTCCCCTG GCAATGTAGGTGTAGGTAAAGCTGATGGTGATTGGGAGGCTGGGAGACATACGCATGGTCCCCTG A T TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:24018543..24018848 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_101898,RMVar_hsa_circ_189245 113783 RMVar_ID_113783 Human_SNP_ID_831384923 m1A Human chr18 - 8825140 8825140 8825140 CCTCTGGCTCTGCTTGTGGGAAAGGGACCCTCACCACCTGCCGCCGTGATGCTGTCGACCCTGCG CCTCTGGCTCTGCTTGTGGGAAAGGGACCCTCGCCACCTGCCGCCGTGATGCTGTCGACCCTGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:8825090..8825190 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung 113784 RMVar_ID_113784 Human_SNP_ID_831427911 m1A Human chr18 - 80109344 80109344 80109344 CGCCCGCCCGCGCCTCCGCCCCGCGCGGCGGGACCCCCGCCTCAGCGCGCGCCCACCCCCAGCGC CGCCCGCCCGCGCCTCCGCCCCGCGCGGCGGGCCCCCCGCCTCAGCGCGCGCCCACCCCCAGCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:80109276..80109450 26863196 MeRIP-seq:(Medium) rs954196530 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113785 RMVar_ID_113785 Human_SNP_ID_831497517 m1A Human chr18 + 12635091 12635091 12635091 TACCTCTGTTTCCATACATTGTGAATATCCCAATTTACCTGTAATAAAAATGAAAAGGATTACTT TACCTCTGTTTCCATACATTGTGAATATCCCATTTTACCTGTAATAAAAATGAAAAGGATTACTT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:12635013..12635169 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 113786 RMVar_ID_113786 Human_SNP_ID_831642821 m1A Human chr18 - 12308106 12308106 12308106 GCCGCGGCCCGGCCTGCAGCAGCCGAGGGAGGACGCGCGGGCGCCAGTCGGGGGACCCTTGCCGG GCCGCGGCCCGGCCTGCAGCAGCCGAGGGAGGGCGCGCGGGCGCCAGTCGGGGGACCCTTGCCGG T C lnc-AFG3L2-4,lnc-AFG3L2-4:2,lnc-AFG3L2-4:3 RNACentral:URS0000D581FA,RNACentral:URS0000D572C0,RNACentral:URS0000D5C389 lincRNA,lincRNA,lincRNA exon,exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:12308000..12308108 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 2 breast 113787 RMVar_ID_113787 Human_SNP_ID_831673641 m1A Human chr18 - 12308618 12308618 12308618 ACCCAGAGCCCGGGACGCCGCCACCCGCGCCCACCCCAGGCGCCCCGGCGGCCGAATTCCAGGCG ACCCAGAGCCCGGGACGCCGCCACCCGCGCCCCCCCCAGGCGCCCCGGCGGCCGAATTCCAGGCG T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr18:12308610..12308750 26863196 MeRIP-seq:(Medium) rs937326026 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113788 RMVar_ID_113788 Human_SNP_ID_831674167 m1A Human chr18 - 31102005 31102005 31102005 CTCGCCCCGCGGAGCCCTCCTACCCCGGCCCGACGCTCGGCCCGCGACCTGCCCCGAGCCCTCTC CTCGCCCCGCGGAGCCCTCCTACCCCGGCCCGGCGCTCGGCCCGCGACCTGCCCCGAGCCCTCTC T C DSC2 Ensembl:ENSG00000134755 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:31101901..31102075 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_238758,Human_RBP_ID_9327741,Human_RBP_ID_22445953 113789 RMVar_ID_113789 Human_SNP_ID_831677233 m1A Human chr18 - 75209185 75209185 75209185 CGGGCGACGCGGGGAAGGGGGGAGCCAGGGGGAGGGCGCCGGCCGGAGGAGGGGCGGACCCGCCC CGGGCGACGCGGGGAAGGGGGGAGCCAGGGGGGGGGCGCCGGCCGGAGGAGGGGCGGACCCGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:75208783..75209360 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3561238,Human_RBP_ID_4494049,Human_RBP_ID_5369459,Human_RBP_ID_26783276 113790 RMVar_ID_113790 Human_SNP_ID_831678105 m1A Human chr18 + 8825822 8825822 8825822 CCACCACCACAAGGGAGAGCCCCGTGCACACCACCATTAATGATGGCCTCTCCAGCCTCTTCAAC CCACCACCACAAGGGAGAGCCCCGTGCACACCGCCATTAATGATGGCCTCTCCAGCCTCTTCAAC A G MTCL1 Ensembl:ENSG00000168502 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:8825776..8825850 26863196 MeRIP-seq:(Medium) rs747047832 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 7 large intestine RMVar_hsa_circ_99748,RMVar_hsa_circ_188490,RMVar_hsa_circ_188491,RMVar_hsa_circ_336156 113791 RMVar_ID_113791 Human_SNP_ID_831678280 m1A Human chr18 + 50392269 50392269 50392269 TTATAACCTGAGTCCCTTGTGAACTTTTGAACATACCAACAGGGTATAGAGTATAGAGGCTATTT TTATAACCTGAGTCCCTTGTGAACTTTTGAACCTACCAACAGGGTATAGAGTATAGAGGCTATTT A C SKA1 Ensembl:ENSG00000154839 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10460085 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_6691999,Human_RBP_ID_13320054,Human_RBP_ID_26463769 GWAS_ID_11862,GWAS_ID_11863,GWAS_ID_11864,GWAS_ID_11865,GWAS_ID_11866 RMVar_hsa_circ_84889,RMVar_hsa_circ_118795,RMVar_hsa_circ_190132,RMVar_hsa_circ_82060,RMVar_hsa_circ_190133,RMVar_hsa_circ_190134 113792 RMVar_ID_113792 Human_SNP_ID_831704395 m1A Human chr18 - 23586696 23586696 23586696 GGAAAGCATCACGGCCAGAAACCGTTGGCACAACTCCACAGATACTCTCCCGGGCCGAGCCAGAC GGAAAGCATCACGGCCAGAAACCGTTGGCACAGCTCCACAGATACTCTCCCGGGCCGAGCCAGAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:23586646..23586759 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113793 RMVar_ID_113793 Human_SNP_ID_831727212 m1A Human chr18 - 2538789 2538789 2538789 TTGAGTTGCACTAACATTCTATGTTATTCTAGACTATACAAATTAAGTGGTAAGCAGTTATAAAG TTGAGTTGCACTAACATTCTATGTTATTCTAGGCTATACAAATTAAGTGGTAAGCAGTTATAAAG T C METTL4 Ensembl:ENSG00000101574 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11663148 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22390400 Human_miRNA_ID_1554126,Human_miRNA_ID_1556011,Human_miRNA_ID_1557793,Human_miRNA_ID_1570198,Human_miRNA_ID_1576580,Human_miRNA_ID_1583732,Human_miRNA_ID_1617703,Human_miRNA_ID_1662003,Human_miRNA_ID_1663223,Human_miRNA_ID_1682119 GWAS_ID_8305 113794 RMVar_ID_113794 Human_SNP_ID_831775771 m1A Human chr18 + 46091826 46091826 46091826 ACAGAGGTATCAGCTCCAAGAATACGCTCTTCAAGAATAGAGGACATCTCAGCAGTCCCTATGGA ACAGAGGTATCAGCTCCAAGAATACGCTCTTCCAGAATAGAGGACATCTCAGCAGTCCCTATGGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr18:46089495..46091875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113795 RMVar_ID_113795 Human_SNP_ID_831797830 m1A Human chr18 - 8784469 8784469 8784469 CCGCTGGGCCTCGTGTTTTAGGGTCACTAGGTACTCAGAGTCCTCCCGGGCCTTCAGGAGCTCCG CCGCTGGGCCTCGTGTTTTAGGGTCACTAGGTGCTCAGAGTCCTCCCGGGCCTTCAGGAGCTCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:8784426..8784625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 113796 RMVar_ID_113796 Human_SNP_ID_831881175 m1A Human chr18 + 63318007 63318007 63318007 TCGCCGGCTCCACAGCCTCCCATTGCCCCAGGAGCCCACCCGCACTCCAACCCCCGCATCTCGGA TCGCCGGCTCCACAGCCTCCCATTGCCCCAGGGGCCCACCCGCACTCCAACCCCCGCATCTCGGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63317961..63318183 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113797 RMVar_ID_113797 Human_SNP_ID_831934127 m1A Human chr18 + 75209045 75209045 75209045 ACATGTCCACGATGGCCCGGGCCCCGGTGGGCACCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC ACATGTCCACGATGGCCCGGGCCCCGGTGGGCCCCAGCCGCAGCATGGCCTGCGCCTCCGCCCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr18:75208862..75209108 26863410 MeRIP-seq:(Medium) rs200768449 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,LUSC 2 head and neck 113798 RMVar_ID_113798 Human_SNP_ID_831996680 m1A Human chr18 - 267995 267994 267995 CCGAGAAGATGTCTCCGACGCCGCCGCTCTTCAGTTTGCCCGAAGCGCGGACGCGGTTTACGGTG CCGAGAAGATGTCTCCGACGCCGCCGCTCTTC_GTTTGCCCGAAGCGCGGACGCGGTTTACGGTG CT C THOC1 Ensembl:ENSG00000079134 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:267929..267994 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 KIRP 1 - Human_RBP_ID_823113,Human_RBP_ID_4494080,Human_RBP_ID_9379455,Human_RBP_ID_18420637,Human_RBP_ID_26334517,Human_RBP_ID_27814452 Human_Splice_Rec_1887427,Human_Splice_Rec_1887463,Human_Splice_Rec_1887549,Human_Splice_Rec_1887599,Human_Splice_Rec_1887635,Human_Splice_Rec_1887717,Human_Splice_Rec_1887743,Human_Splice_Rec_1887755,Human_Splice_Rec_1887771,Human_Splice_Rec_1887777,Human_Splice_Rec_1887781 RMVar_hsa_circ_13118 113799 RMVar_ID_113799 Human_SNP_ID_832026981 m1A Human chr18 + 36067496 36067496 36067496 CCGCCCTAGCTGCGGCCTCGCCCCCTCACCCCACCCTTCCCCACGCTCTCACCACGGCCGCCGCT CCGCCCTAGCTGCGGCCTCGCCCCCTCACCCCCCCCTTCCCCACGCTCTCACCACGGCCGCCGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:36067276..36067550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 8 biliary tract,gallbladder 113800 RMVar_ID_113800 Human_SNP_ID_832036340 m1A Human chr18 + 45955326 45955326 45955326 TTCACTGGACTCTTCCCTCTGAGGAGTTTCATACTTCTTCTTTTCCTAAAAACAACATACATAAT TTCACTGGACTCTTCCCTCTGAGGAGTTTCATTCTTCTTCTTTTCCTAAAAACAACATACATAAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:45955276..45967282;chr18:45955276..45967299;chr18:45955276..45955384 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 113801 RMVar_ID_113801 Human_SNP_ID_832045962 m1A Human chr18 - 12948076 12948076 12948076 CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCAGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA CCCGCGCCTCCGAAGAGGACAGTGGCGGCGGCGGCGGCGGCGGCGCGTGGCCCGTAGCCTAGCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr18:12948026..12948162;chr18:12946928..12948100 26863196 MeRIP-seq:(Medium) rs960331800 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,COCA,large_intestine adenocarcinoma 8 stomach,large intestine 113802 RMVar_ID_113802 Human_SNP_ID_832073898 m1A Human chr18 - 63422424 63422424 63422424 AAGTTTGGTGGGGAGGGTCGGAGCTCTGGTGGAGAGAGTGTTGTCTAAAACAAGTTCCGGAAGGG AAGTTTGGTGGGGAGGGTCGGAGCTCTGGTGGCGAGAGTGTTGTCTAAAACAAGTTCCGGAAGGG T G VPS4B Ensembl:ENSG00000119541 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:63422234..63422475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4496581,Human_RBP_ID_6701316 113803 RMVar_ID_113803 Human_SNP_ID_832082658 m1A Human chr18 + 48951472 48951472 48951472 TGCGCTCCTGGGGGCCCAGGTCCTCGGCGGGGACTTCCTCGAGGCTGGCGCGGGCGCAGGGGCAG TGCGCTCCTGGGGGCCCAGGTCCTCGGCGGGGGCTTCCTCGAGGCTGGCGCGGGCGCAGGGGCAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr18:48951426..48951575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113804 RMVar_ID_113804 Human_SNP_ID_832106708 m1A Human chr18 + 662247 662247 662247 TTTTTGGACAGCCTGGGATTCTCCACCAGAGAAGAAGGGGACTTGGGCCCAGTTTATGGCTTCCA TTTTTGGACAGCCTGGGATTCTCCACCAGAGAGGAAGGGGACTTGGGCCCAGTTTATGGCTTCCA A G TYMS Ensembl:ENSG00000176890 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:662198..662371 26863196 MeRIP-seq:(Medium) rs3786362 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 9 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_52161,Human_RBP_ID_510512,Human_RBP_ID_905563,Human_RBP_ID_1551463,Human_RBP_ID_1877701,Human_RBP_ID_4491300,Human_RBP_ID_5144539,Human_RBP_ID_6701760,Human_RBP_ID_13330952,Human_RBP_ID_18719296,Human_RBP_ID_18993252,Human_RBP_ID_22445846,Human_RBP_ID_23776195,Human_RBP_ID_26769652 Human_Splice_Rec_1887967,Human_Splice_Rec_1887979,Human_Splice_Rec_1887993 Human_miRNA_ID_3118844 RMVar_hsa_circ_12080,RMVar_hsa_circ_188190,RMVar_hsa_circ_319629,RMVar_hsa_circ_361301,RMVar_hsa_circ_188191,RMVar_hsa_circ_280930,RMVar_hsa_circ_288395,RMVar_hsa_circ_25599,RMVar_hsa_circ_188192 113805 RMVar_ID_113805 Human_SNP_ID_832152297 m1A Human chr18 - 62187591 62187591 62187591 GAAGTACTGCCCGCCGTTCCTCTGTTGCAGCTACCTCGTCATCGTCCTCATCCGAATCACTGAGA GAAGTACTGCCCGCCGTTCCTCTGTTGCAGCTTCCTCGTCATCGTCCTCATCCGAATCACTGAGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:62187339..62187798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin Merkel_cell_carcinoma,leg Merkel_cell_carcinoma 3 skin,lower extremity 113806 RMVar_ID_113806 Human_SNP_ID_832154649 m1A Human chr18 + 79988389 79988389 79988389 CCAGCCGTTGTGCAGGTGCGGGAGCATGTACGACATGGCGGCCCGCGCGCTCGCCGCCGCCCAAG CCAGCCGTTGTGCAGGTGCGGGAGCATGTACGGCATGGCGGCCCGCGCGCTCGCCGCCGCCCAAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr18:79988298..79988550;chr18:79988310..79988520 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113807 RMVar_ID_113807 Human_SNP_ID_832159002 m1A Human chr18 - 39594057 39594057 39594057 AAGAAAAGAAGTAGACAGGAAGGGAAGAAACAAGGAAGAAAGGACAGAGAGAAAGATTTATAATA AAGAAAAGAAGTAGACAGGAAGGGAAGAAACAGGGAAGAAAGGACAGAGAGAAAGATTTATAATA T C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr18:39594048..39594131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113808 RMVar_ID_113808 Human_SNP_ID_832190433 m1A Human chr18 + 228145 228145 228145 ACTCAGGCTGTTAGTTCCTTGCCCTTAACTCCACGGACAGGCCCATCTCTGCTCCAGCTACCCAC ACTCAGGCTGTTAGTTCCTTGCCCTTAACTCCGCGGACAGGCCCATCTCTGCTCCAGCTACCCAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr18:228142..228273 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113809 RMVar_ID_113809 Human_SNP_ID_832204316 m1A Human chr18 + 49491732 49491732 49491732 AAGGTGTCCTAAGAAATGCCATCATCGCAGCCATACTTTCCCCCACCAAGGGCTTGCTTTCCCTT AAGGTGTCCTAAGAAATGCCATCATCGCAGCCGTACTTTCCCCCACCAAGGGCTTGCTTTCCCTT A G AC100778.3 Ensembl:ENSG00000265496 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr18:49491701..49492473 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas 113810 RMVar_ID_113810 Human_SNP_ID_832215590 m1A Human chr18 - 32287541 32287541 32287541 GCTGTCCGTGATGTGAAAACCGACTGGAATGAAGAATGCAAGAGCCCCAAGAAGGGTCGGTGCTC GCTGTCCGTGATGTGAAAACCGACTGGAATGAGGAATGCAAGAGCCCCAAGAAGGGTCGGTGCTC T C GAREM1 Ensembl:ENSG00000141441 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs16962977 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_6680327 GWAS_ID_7875,GWAS_ID_7876,GWAS_ID_7877 RMVar_hsa_circ_189505,RMVar_hsa_circ_39701,RMVar_hsa_circ_361928,RMVar_hsa_circ_189503,RMVar_hsa_circ_75394,RMVar_hsa_circ_324248,RMVar_hsa_circ_324757,RMVar_hsa_circ_189506,RMVar_hsa_circ_189504 113811 RMVar_ID_113811 Human_SNP_ID_862324453 m1A Human chr6 - 26156386 26156386 26156386 CGGGCGCGGCAGGCGCAGTCTCGGACATGTTGAAGGCAAGCGTGAGCGAGAGCAATTCGAGCCGG CGGGCGCGGCAGGCGCAGTCTCGGACATGTTGGAGGCAAGCGTGAGCGAGAGCAATTCGAGCCGG T C lnc-HIST1H4D-3 RNACentral:URS0000D5AA68 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr6:26156326..26156550;chr6:26156326..26156601;chr6:26156326..26156534 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 2 stomach RMVar_hsa_circ_76721,RMVar_hsa_circ_237739 113812 RMVar_ID_113812 Human_SNP_ID_862327111 m1A Human chr6 + 7910700 7910698 7910701 GGGCGCCCCAGCGCCCGCCGCCGCCATGGCCCAGCAGCAGCAGCAGCAGCGCAGTCAGGGCCGCC GGGCGCCCCAGCGCCCGCCGCCGCCATGGCC___CAGCAGCAGCAGCAGCGCAGTCAGGGCCGCC CCAG C - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr6:7910599..7910780 26863410 MeRIP-seq:(Medium) rs775841007 Functional Loss DEL ICGC 32..34 33 CHOL 1 - 113813 RMVar_ID_113813 Human_SNP_ID_862328357 m1A Human chr6 + 133285809 133285809 133285809 TGCTAATGTATGGGTTATGGATTATGATAGAAAGAAAGGTGTCAGACATAACTTCAAGGTCTTTG TGCTAATGTATGGGTTATGGATTATGATAGAATGAAAGGTGTCAGACATAACTTCAAGGTCTTTG A T EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:133285802..133285924 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_24135541 RMVar_hsa_circ_1637,RMVar_hsa_circ_241586,RMVar_hsa_circ_374745 113814 RMVar_ID_113814 Human_SNP_ID_862355913 m1A Human chr6 + 54210202 54210202 54210202 GCCAGAGCAGCTGCTTGTCTGCAGCAGGACACAGTTCCTACATACGTTTCAGTTCTTTCATGGTA GCCAGAGCAGCTGCTTGTCTGCAGCAGGACACGGTTCCTACATACGTTTCAGTTCTTTCATGGTA A G MLIP Ensembl:ENSG00000146147 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs139254516 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_26861,RMVar_hsa_circ_356542,RMVar_hsa_circ_239018,RMVar_hsa_circ_334360,RMVar_hsa_circ_302058,RMVar_hsa_circ_63697,RMVar_hsa_circ_239020,RMVar_hsa_circ_295015,RMVar_hsa_circ_357155 113815 RMVar_ID_113815 Human_SNP_ID_862357210 m1A Human chr6 - 33672100 33672100 33672100 CCCAGCAGACAGGCTGGGGGCACTGAAGACGGACTGCTTGCGGCTCAGCACCATGGTGGACATCA CCCAGCAGACAGGCTGGGGGCACTGAAGACGGTCTGCTTGCGGCTCAGCACCATGGTGGACATCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33672051..33672200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 4 uterus 113816 RMVar_ID_113816 Human_SNP_ID_862368159 m1A Human chr6 - 33684127 33684127 33684127 AAGCCCCCACTCTCGCAGCGCTGGTAGGCCTCACTGCCCTCCAGGAAGAGCAGCTCAGGCCAGTG AAGCCCCCACTCTCGCAGCGCTGGTAGGCCTCGCTGCCCTCCAGGAAGAGCAGCTCAGGCCAGTG T C lnc-UQCC2-1 RNACentral:URS0000D58C07 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33684076..33684150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113817 RMVar_ID_113817 Human_SNP_ID_862387062 m1A Human chr6 + 169562779 169562779 169562779 CATAGAAACTGGTTAAAAAAGAAAAAATCTGTACAATCTGCAGAAGTGAAATAAGGAACAGCGAG CATAGAAACTGGTTAAAAAAGAAAAAATCTGTGCAATCTGCAGAAGTGAAATAAGGAACAGCGAG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:169562675..169562802 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 113818 RMVar_ID_113818 Human_SNP_ID_862398946 m1A Human chr6 + 3064015 3064015 3064015 CGCAGCAGCAGGGCCCGGTCCTGCGCCTCGGGAGTCGGCGTCCAGGCTCGGAGCGCGACACGGAG CGCAGCAGCAGGGCCCGGTCCTGCGCCTCGGGGGTCGGCGTCCAGGCTCGGAGCGCGACACGGAG A G RIPK1 Ensembl:ENSG00000137275 Protein coding exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:3063969..3064111 26863196 MeRIP-seq:(Medium) rs12203636 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_Splice_Rec_733791 113819 RMVar_ID_113819 Human_SNP_ID_862407057 m1A Human chr6 + 31797741 31797738 31797741 GGTTATGGGTCACCAATGAAAGAGGGAGGGGAAGAGGAGGAGGAGCCATCACTGTTTCTGCTGCA GGTTATGGGTCACCAATGAAAGAGGGAGGG___GAGGAGGAGGAGCCATCACTGTTTCTGCTGCA GGAA G RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31797676..31797827 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 STAD 1 - 113820 RMVar_ID_113820 Human_SNP_ID_862420474 m1A Human chr6 + 43777725 43777725 43777725 GGGGGGATAGGGAGGGGGGTAACACTTTGGGAACAGGTGGTCCCAGGTCGTTTCCTGGCTAGATT GGGGGGATAGGGAGGGGGGTAACACTTTGGGAGCAGGTGGTCCCAGGTCGTTTCCTGGCTAGATT A G VEGFA Ensembl:ENSG00000112715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43777720..43777814 26863196 MeRIP-seq:(Medium) rs1219979424 Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_79816,Human_RBP_ID_789998,Human_RBP_ID_841263,Human_RBP_ID_947738,Human_RBP_ID_3822187,Human_RBP_ID_3969154,Human_RBP_ID_5090314,Human_RBP_ID_5122281,Human_RBP_ID_5217309,Human_RBP_ID_5398262,Human_RBP_ID_8143751,Human_RBP_ID_8237122,Human_RBP_ID_9350236,Human_RBP_ID_9437477,Human_RBP_ID_9444317,Human_RBP_ID_17663140,Human_RBP_ID_18957483,Human_RBP_ID_19129447,Human_RBP_ID_22105187,Human_RBP_ID_22365559,Human_RBP_ID_22418770,Human_RBP_ID_22682940,Human_RBP_ID_22746261,Human_RBP_ID_22773096,Human_RBP_ID_24436359,Human_RBP_ID_26354020,Human_RBP_ID_26771991,Human_RBP_ID_26792448 RMVar_hsa_circ_33572,RMVar_hsa_circ_238728,RMVar_hsa_circ_102569,RMVar_hsa_circ_322948,RMVar_hsa_circ_74333,RMVar_hsa_circ_350327,RMVar_hsa_circ_324506,RMVar_hsa_circ_238730 113821 RMVar_ID_113821 Human_SNP_ID_862448101 m1A Human chr6 - 133441639 133441639 133441639 CTGGATAACCATTTTTTTCCACCAGACCACTCACCCTGTCACTCTCTTTAAATTAGCCAATCAGA CTGGATAACCATTTTTTTCCACCAGACCACTCTCCCTGTCACTCTCTTTAAATTAGCCAATCAGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:133441619..133441818 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 9 breast 113822 RMVar_ID_113822 Human_SNP_ID_862450124 m1A Human chr6 - 26216570 26216568 26216571 TTCCAAGAAGGCTGTGACCAAGGCGCAGAAGAAGGATGGCAAGAAGCGCAAGCGCAGTCGTAAGG TTCCAAGAAGGCTGTGACCAAGGCGCAGAAG___GATGGCAAGAAGCGCAAGCGCAGTCGTAAGG CCTT C H2BC8 Ensembl:ENSG00000273802 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26216519..26216643 26863196 MeRIP-seq:(Medium) rs763480943 Functional Loss DEL TCGA,ICGC 32..34 33 STAD 2 - Human_RBP_ID_1111442,Human_RBP_ID_4905376,Human_RBP_ID_5478663,Human_RBP_ID_9336001,Human_RBP_ID_9400099,Human_RBP_ID_22104720,Human_RBP_ID_22460481,Human_RBP_ID_24548356,Human_RBP_ID_26353130 RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_237747,RMVar_hsa_circ_378737 113823 RMVar_ID_113823 Human_SNP_ID_862462210 m1A Human chr6 - 7339454 7339454 7339454 AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGATGCGAGTTACACCAACCAGGACAGAAATCATT AGCTGGCTGAAGATGGCTACTCTGGAGTTGAGGTGCGAGTTACACCAACCAGGACAGAAATCATT T C AL139095.2,SSR1,CAGE1 Ensembl:ENSG00000220472,Ensembl:ENSG00000124783,Ensembl:ENSG00000164304 Pseudogene,Protein coding,Protein coding exon,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs780641426 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_17711605 113824 RMVar_ID_113824 Human_SNP_ID_862490476 m1A Human chr6 + 4031582 4031582 4031582 TATTTATAGGATGGAAGATGCTAATTCTGAAAAGAGTATAAATGAAGAAAATGGAGAAGTATCAG TATTTATAGGATGGAAGATGCTAATTCTGAAAGGAGTATAAATGAAGAAAATGGAGAAGTATCAG A G PRPF4B Ensembl:ENSG00000112739 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:4031551..4031600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_251366,Human_RBP_ID_949009,Human_RBP_ID_2021044,Human_RBP_ID_3007445,Human_RBP_ID_3969497,Human_RBP_ID_9401480,Human_RBP_ID_26353315,Human_RBP_ID_27098019 Human_Splice_Rec_734452,Human_Splice_Rec_734482 Human_miRNA_ID_1789148 RMVar_hsa_circ_58849,RMVar_hsa_circ_111498,RMVar_hsa_circ_236967,RMVar_hsa_circ_102759,RMVar_hsa_circ_236968,RMVar_hsa_circ_326913,RMVar_hsa_circ_358863,RMVar_hsa_circ_121680,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 113825 RMVar_ID_113825 Human_SNP_ID_862503403 m1A Human chr6 + 43513414 43513414 43513414 TCCCATGGAGTAGGATAGCAACCAGAGTGAAGACCAGCATGAGAGGTCCATAGAGTTCACCTGCA TCCCATGGAGTAGGATAGCAACCAGAGTGAAGTCCAGCATGAGAGGTCCATAGAGTTCACCTGCA A T POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43513351..43513477 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113826 RMVar_ID_113826 Human_SNP_ID_862516386 m1A Human chr6 - 28896287 28896287 28896287 GCCGAGTGGTCTAAGGCGCCAGACTCAAGCTAAGCTTCCTCCGCGGTGGGGATTCTGGTCTCCAA GCCGAGTGGTCTAAGGCGCCAGACTCAAGCTAGGCTTCCTCCGCGGTGGGGATTCTGGTCTCCAA T C TRL-CAA1-1-001,tRNA-Leu,tRNA-Leu:2,tRNA-Leu-CAA-1-1,TRL-CAA1-1-001:2 RNACentral:URS0000224A3A,RNACentral:URS00004AEFEF,RNACentral:URS000044259A,RNACentral:URS0000747665,RNACentral:URS000071E759 tRNA,tRNA,tRNA,tRNA,tRNA intron,intron,intron,intron,exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:28896203..28896357 26863196 MeRIP-seq:(Medium) rs1358654044 Functional Loss SNV ICGC 33..33 33 UTCA 1 - Human_RBP_ID_660302,Human_RBP_ID_1216994,Human_RBP_ID_1245649,Human_RBP_ID_1394941,Human_RBP_ID_1669933,Human_RBP_ID_2017568,Human_RBP_ID_3001980,Human_RBP_ID_3805315,Human_RBP_ID_4878077,Human_RBP_ID_5622217,Human_RBP_ID_7589240,Human_RBP_ID_8270050,Human_RBP_ID_8641139,Human_RBP_ID_8899538,Human_RBP_ID_9193200,Human_RBP_ID_15778064,Human_RBP_ID_17092154,Human_RBP_ID_17306216,Human_RBP_ID_17710372,Human_RBP_ID_18072630,Human_RBP_ID_18369887,Human_RBP_ID_18450049,Human_RBP_ID_18519246,Human_RBP_ID_18539025,Human_RBP_ID_18861853,Human_RBP_ID_21319103,Human_RBP_ID_22830900,Human_RBP_ID_23110818,Human_RBP_ID_23138746,Human_RBP_ID_24179882,Human_RBP_ID_24513771,Human_RBP_ID_26534919,Human_RBP_ID_26714547,Human_RBP_ID_27161048,Human_RBP_ID_27344808,Human_RBP_ID_27754628 113827 RMVar_ID_113827 Human_SNP_ID_862536956 m1A Human chr6 - 31355577 31355575 31355577 CTGACTCTTCCCATCAGACCCCCCAAAGACACACGTGACCCACCACCCCATCTCTGACCATGAGG CTGACTCTTCCCATCAGACCCCCCAAAGACAC__GTGACCCACCACCCCATCTCTGACCATGAGG CGT C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31355526..31355600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 COAD,HNSC 2 - Human_RBP_ID_18073440,Human_RBP_ID_22773903 Human_Splice_Rec_751778,Human_Splice_Rec_751792,Human_Splice_Rec_751806,Human_Splice_Rec_751810 113828 RMVar_ID_113828 Human_SNP_ID_862552567 m1A Human chr6 - 31356287 31356287 31356287 CCTGGACCGCCGCGGACACGGCGGCTCAGATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG CCTGGACCGCCGCGGACACGGCGGCTCAGATCTCCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCG T A HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:31356226..31356468;chr6:31356226..31356499 26863196 MeRIP-seq:(Medium) rs41541519 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_790740,Human_RBP_ID_842139,Human_RBP_ID_18472044,Human_RBP_ID_22461068,Human_RBP_ID_22773396 Human_miRNA_ID_2867548 GWAS_ID_9126 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 113829 RMVar_ID_113829 Human_SNP_ID_862580260 m1A Human chr6 + 126340289 126340289 126340289 GGTACTTGACAGAGAGGATGGCGCTGTCGACCATAGTCTCCCAGAGGAAGCAGATAAAGCGGAAG GGTACTTGACAGAGAGGATGGCGCTGTCGACCGTAGTCTCCCAGAGGAAGCAGATAAAGCGGAAG A G CENPW Ensembl:ENSG00000203760 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:126340151..126340400 32194978 MeRIP-seq:(Medium) rs750494370 Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_1324502,Human_RBP_ID_1663819,Human_RBP_ID_2008013,Human_RBP_ID_4905590,Human_RBP_ID_5478752,Human_RBP_ID_7536565,Human_RBP_ID_9336769,Human_RBP_ID_9401071,Human_RBP_ID_18063404,Human_RBP_ID_18853753,Human_RBP_ID_22462885,Human_RBP_ID_24133509,Human_RBP_ID_25961655 Human_miRNA_ID_937616,Human_miRNA_ID_957776,Human_miRNA_ID_2423809,Human_miRNA_ID_2433468,Human_miRNA_ID_2585549 RMVar_hsa_circ_241352,RMVar_hsa_circ_119445 113830 RMVar_ID_113830 Human_SNP_ID_862584874 m1A Human chr6 - 24701575 24701571 24701575 CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATTAATTTTCCTGTGGCCTTGTTGGTCAGATCCACA CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATT____TTCCTGTGGCCTTGTTGGTCAGATCCACA AAATT A AL031775.1 Ensembl:ENSG00000272345 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24701525..24701605 26863196 MeRIP-seq:(Medium) rs746562084 Functional Loss DEL TCGA 33..36 33 STAD 1 - Human_RBP_ID_3000481,Human_RBP_ID_3803848 113831 RMVar_ID_113831 Human_SNP_ID_862607593 m1A Human chr6 - 143843407 143843407 143843407 GATGACACCCTCGAAGTCCGGCGGGGAGACCAAGGTCCAGCTGAAGGCCGCTTCTGTAGGCCTCA GATGACACCCTCGAAGTCCGGCGGGGAGACCACGGTCCAGCTGAAGGCCGCTTCTGTAGGCCTCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:143835882..143844617 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113832 RMVar_ID_113832 Human_SNP_ID_862632707 m1A Human chr6 - 34242780 34242780 34242780 CCCATCTCAAGTCTCACCCGGGTCTTGGCAGCACCCTTGTTTTTGCTTCCCTTTGGTCGGCCCCG CCCATCTCAAGTCTCACCCGGGTCTTGGCAGCGCCCTTGTTTTTGCTTCCCTTTGGTCGGCCCCG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:34242751..34242800 26863196 MeRIP-seq:(Medium) rs1207411040 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 113833 RMVar_ID_113833 Human_SNP_ID_862633994 m1A Human chr6 + 136249824 136249824 136249824 TCCCCAGCCATGTGGAATGCCCATCCCTCCTCACTCTTTTAAAATGAGAAGCATGAATTCCAGAT TCCCCAGCCATGTGGAATGCCCATCCCTCCTCGCTCTTTTAAAATGAGAAGCATGAATTCCAGAT A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:136249822..136249949 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113834 RMVar_ID_113834 Human_SNP_ID_862644893 m1A Human chr6 + 30550178 30550178 30550178 CCACTTATATCCATCAATGGTTCCCCAAATTTAAATCTTTCCCAAATTCAAATTTCCGTCCTCTT CCACTTATATCCATCAATGGTTCCCCAAATTTTAATCTTTCCCAAATTCAAATTTCCGTCCTCTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30550176..30550264 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113835 RMVar_ID_113835 Human_SNP_ID_862670269 m1A Human chr6 + 32843893 32843893 32843893 GGGGTAAAGCGAGCTCTGGAGATCGCATAGAGAAACTGTAGTGTCCTGGGTCCGAGCGACGCCCG GGGGTAAAGCGAGCTCTGGAGATCGCATAGAGGAACTGTAGTGTCCTGGGTCCGAGCGACGCCCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32843827..32843985 26863196 MeRIP-seq:(Medium) rs374038167 Functional Loss SNV ICGC 33..33 33 MALY 1 - 113836 RMVar_ID_113836 Human_SNP_ID_862670587 m1A Human chr6 - 113857642 113857633 113857642 CGGGGCGAGCAGCAGCAGCAGCGGCGGCGGCAACAGCGGCAGCGGCACACACACCGGAGGGAGGG CGGGGCGAGCAGCAGCAGCAGCGGCGGCGGCA_________GCGGCACACACACCGGAGGGAGGG CTGCCGCTGT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:113857593..113857760 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..41 33 STAD 1 - 113837 RMVar_ID_113837 Human_SNP_ID_862679848 m1A Human chr6 - 30571562 30571562 30571562 CTCTGCTCGTTTCTTCCTTGCCTACCAGCCTCACCTGATGGGCTCGTGCTCTCTCCGTCCCCGAT CTCTGCTCGTTTCTTCCTTGCCTACCAGCCTCGCCTGATGGGCTCGTGCTCTCTCCGTCCCCGAT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:30571471..30571575 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus 113838 RMVar_ID_113838 Human_SNP_ID_862694241 m1A Human chr6 + 43020792 43020792 43020792 TGAGCCTGCTGTCATCTTCACTGCCCCTGCCCATCTGTCACCCACCTGCTCCTTTGACCCCTGGA TGAGCCTGCTGTCATCTTCACTGCCCCTGCCCGTCTGTCACCCACCTGCTCCTTTGACCCCTGGA A G KLHDC3 Ensembl:ENSG00000124702 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:43020751..43020800 26863196 MeRIP-seq:(Medium) rs902324856 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_664876,Human_RBP_ID_792111,Human_RBP_ID_17663753,Human_RBP_ID_18076919,Human_RBP_ID_26828535 113839 RMVar_ID_113839 Human_SNP_ID_862696204 m1A Human chr6 + 63579308 63579308 63579308 CTAGCATTAATTGAAGGTGGAATGAAATACGAAGATGCAGTACAATTCATAAGACAGTAAGTAAT CTAGCATTAATTGAAGGTGGAATGAAATACGACGATGCAGTACAATTCATAAGACAGTAAGTAAT A C PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:63579225..63579365 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_1675394,Human_RBP_ID_2024716,Human_RBP_ID_3813357,Human_RBP_ID_7621623,Human_RBP_ID_15863555,Human_RBP_ID_27757567 Human_Splice_Rec_782118,Human_Splice_Rec_782119,Human_Splice_Rec_782138,Human_Splice_Rec_782139,Human_Splice_Rec_782148,Human_Splice_Rec_782149,Human_Splice_Rec_782158,Human_Splice_Rec_782159,Human_Splice_Rec_782174,Human_Splice_Rec_782175,Human_Splice_Rec_782184,Human_Splice_Rec_782185 Human_miRNA_ID_622083 RMVar_hsa_circ_314933,RMVar_hsa_circ_358170 113840 RMVar_ID_113840 Human_SNP_ID_862704862 m1A Human chr6 + 4892002 4892002 4892002 CTCTCCTAAGGCACTCGTGATTGGGAAAGACCACGAATCCAAAAACAGCCAGCTGTTTGCTGCCA CTCTCCTAAGGCACTCGTGATTGGGAAAGACCGCGAATCCAAAAACAGCCAGCTGTTTGCTGCCA A G CDYL Ensembl:ENSG00000153046 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:4891951..4892300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_9399859,Human_RBP_ID_17308621,Human_RBP_ID_17421444,Human_RBP_ID_18413763,Human_RBP_ID_18867217,Human_RBP_ID_26828983 Human_miRNA_ID_2330910,Human_miRNA_ID_2330911,Human_miRNA_ID_2330912,Human_miRNA_ID_2330913,Human_miRNA_ID_2963992,Human_miRNA_ID_2963993,Human_miRNA_ID_2963994,Human_miRNA_ID_2963995 RMVar_hsa_circ_127308,RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983,RMVar_hsa_circ_117762,RMVar_hsa_circ_107359,RMVar_hsa_circ_236984,RMVar_hsa_circ_345794,RMVar_hsa_circ_236985,RMVar_hsa_circ_278914,RMVar_hsa_circ_236987,RMVar_hsa_circ_236989,RMVar_hsa_circ_24166,RMVar_hsa_circ_236988,RMVar_hsa_circ_236986 113841 RMVar_ID_113841 Human_SNP_ID_862706332 m1A Human chr6 - 30924470 30924470 30924470 GGCCTGGGGGGCAGCCTCTGCCAGAGCTCTTCAGCCAGGAAGGGCATCAGTGGGGCCAGGAGGCG GGCCTGGGGGGCAGCCTCTGCCAGAGCTCTTCTGCCAGGAAGGGCATCAGTGGGGCCAGGAGGCG T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30924420..30924513 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung 113842 RMVar_ID_113842 Human_SNP_ID_862727076 m1A Human chr6 - 16278010 16278010 16278010 CCCCAGTCCTGGTTGTTCTCCCAGTTAGGTCCAGGCCAAGTCGCACTCTGACCTCTTTATCATAC CCCCAGTCCTGGTTGTTCTCCCAGTTAGGTCCCGGCCAAGTCGCACTCTGACCTCTTTATCATAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:16277910..16278029 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113843 RMVar_ID_113843 Human_SNP_ID_862742621 m1A Human chr6 + 15496568 15496568 15496568 GCGGAACTCCAAGAGGAGACTGGAAGAGGCACACCAGGCGGAGAAGCCGCAGTCGCCCCCCAAGA GCGGAACTCCAAGAGGAGACTGGAAGAGGCACGCCAGGCGGAGAAGCCGCAGTCGCCCCCCAAGA A G JARID2 Ensembl:ENSG00000008083 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:15496519..15496791 26863196 MeRIP-seq:(Medium) rs868306515 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_214825,Human_RBP_ID_947352,Human_RBP_ID_3969523,Human_RBP_ID_5532311,Human_RBP_ID_8905102,Human_RBP_ID_9309102,Human_RBP_ID_18425809,Human_RBP_ID_22104618,Human_RBP_ID_22728123,Human_RBP_ID_24548339,Human_RBP_ID_26353415,Human_RBP_ID_26771870,Human_RBP_ID_27574244,Human_RBP_ID_27827311 RMVar_hsa_circ_50801,RMVar_hsa_circ_61103,RMVar_hsa_circ_19729,RMVar_hsa_circ_89803,RMVar_hsa_circ_266036,RMVar_hsa_circ_237259,RMVar_hsa_circ_23857,RMVar_hsa_circ_66832,RMVar_hsa_circ_337833,RMVar_hsa_circ_38132,RMVar_hsa_circ_322175,RMVar_hsa_circ_3965 113844 RMVar_ID_113844 Human_SNP_ID_862742886 m1A Human chr6 - 44003456 44003456 44003456 CCTTCTCCGTGCCTCAAGTGCCAAACGGGGGTACTGCTGCCCTGCGTGCCTTTGCCACTCCTCCC CCTTCTCCGTGCCTCAAGTGCCAAACGGGGGTGCTGCTGCCCTGCGTGCCTTTGCCACTCCTCCC T C AL109615.3 Ensembl:ENSG00000237686 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:44003405..44003510 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast RMVar_hsa_circ_106005,RMVar_hsa_circ_238732 113845 RMVar_ID_113845 Human_SNP_ID_862749475 m1A Human chr6 + 7606152 7606152 7606152 GGAGTAGAAGCCCACATAAAAGAAAAAGAAACAAAGATAAGGATAAAAACTGTGAGTCGAGAAGA GGAGTAGAAGCCCACATAAAAGAAAAAGAAACGAAGATAAGGATAAAAACTGTGAGTCGAGAAGA A G SNRNP48 Ensembl:ENSG00000168566 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7606026..7608825 26863196 MeRIP-seq:(Medium) rs1307196231 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_668234,Human_RBP_ID_5622355,Human_RBP_ID_7628196,Human_RBP_ID_24171612,Human_RBP_ID_24548664 Human_Splice_Rec_736165,Human_Splice_Rec_736187 RMVar_hsa_circ_19055,RMVar_hsa_circ_109071,RMVar_hsa_circ_296659,RMVar_hsa_circ_75458,RMVar_hsa_circ_237073,RMVar_hsa_circ_365189,RMVar_hsa_circ_237074 113846 RMVar_ID_113846 Human_SNP_ID_862790491 m1A Human chr6 - 136361054 136361054 136361054 GGAGAAGGAGGAGCAGCTGCAGCGGCAGGCGGAGGAGCGGGCGCTGCGCGAGCGGGAGGAGGCAG GGAGAAGGAGGAGCAGCTGCAGCGGCAGGCGGGGGAGCGGGCGCTGCGCGAGCGGGAGGAGGCAG T C MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:136360962..136361212 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus Human_Splice_Rec_816335,Human_Splice_Rec_816369,Human_Splice_Rec_816399,Human_Splice_Rec_816431,Human_Splice_Rec_816465,Human_Splice_Rec_816501,Human_Splice_Rec_816535,Human_Splice_Rec_816567,Human_Splice_Rec_816595 RMVar_hsa_circ_59035,RMVar_hsa_circ_269019,RMVar_hsa_circ_366845,RMVar_hsa_circ_266974,RMVar_hsa_circ_75044,RMVar_hsa_circ_241700,RMVar_hsa_circ_369188,RMVar_hsa_circ_265139 113847 RMVar_ID_113847 Human_SNP_ID_862797645 m1A Human chr6 - 26216567 26216563 26216567 CAAGAAGGCTGTGACCAAGGCGCAGAAGAAGGATGGCAAGAAGCGCAAGCGCAGTCGTAAGGAGA CAAGAAGGCTGTGACCAAGGCGCAGAAGAAGG____CAAGAAGCGCAAGCGCAGTCGTAAGGAGA GCCAT G H2BC8 Ensembl:ENSG00000273802 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:26216520..26216641 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..36 33 LUSC 2 - Human_RBP_ID_1111442,Human_RBP_ID_4876296,Human_RBP_ID_5478663,Human_RBP_ID_9336001,Human_RBP_ID_9400099,Human_RBP_ID_22104720,Human_RBP_ID_24548356,Human_RBP_ID_26353130 RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_237747,RMVar_hsa_circ_378737 113848 RMVar_ID_113848 Human_SNP_ID_862806336 m1A Human chr6 - 134174572 134174572 134174572 CTCCTCCTTCATCCACAGCTTTCATGAAGCAGAGGAGGATGGGTCTGAACGACTTTATTCAGAAG CTCCTCCTTCATCCACAGCTTTCATGAAGCAGGGGAGGATGGGTCTGAACGACTTTATTCAGAAG T C SGK1 Ensembl:ENSG00000118515 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:134174462..134174604 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue Human_RBP_ID_81602,Human_RBP_ID_951088,Human_RBP_ID_5217924,Human_RBP_ID_5398375,Human_RBP_ID_9350667,Human_RBP_ID_19017457,Human_RBP_ID_24562415,Human_RBP_ID_26038768 Human_Splice_Rec_813248,Human_Splice_Rec_813249,Human_Splice_Rec_813270,Human_Splice_Rec_813272,Human_Splice_Rec_813273,Human_Splice_Rec_813304,Human_Splice_Rec_813305,Human_Splice_Rec_813326,Human_Splice_Rec_813327,Human_Splice_Rec_813345,Human_Splice_Rec_813366,Human_Splice_Rec_813367,Human_Splice_Rec_813388,Human_Splice_Rec_813389,Human_Splice_Rec_813442,Human_Splice_Rec_813443,Human_Splice_Rec_813458,Human_Splice_Rec_813459,Human_Splice_Rec_813470,Human_Splice_Rec_813471,Human_Splice_Rec_813480,Human_Splice_Rec_813481,Human_Splice_Rec_813488,Human_Splice_Rec_813489,Human_Splice_Rec_813500,Human_Splice_Rec_813501,Human_Splice_Rec_813506,Human_Splice_Rec_813507,Human_Splice_Rec_813510,Human_Splice_Rec_813511,Human_Splice_Rec_813513 RMVar_hsa_circ_33385,RMVar_hsa_circ_68106,RMVar_hsa_circ_44759,RMVar_hsa_circ_124758,RMVar_hsa_circ_241604 113849 RMVar_ID_113849 Human_SNP_ID_862809525 m1A Human chr6 - 31889507 31889495 31889507 GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGAAGAAGAGGAAGATGAGGAGTCAGGGAATCAGTC GAAGAAGAGGAAGAGGAGGAGGAAGAGGAAGA____________TGAGGAGTCAGGGAATCAGTC ATCTTCCTCTTCT A EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31889208..31889634 26863196 MeRIP-seq:(Medium) rs756298483 Functional Loss DEL TCGA 33..44 33 STAD 1 - Human_RBP_ID_214859,Human_RBP_ID_792324,Human_RBP_ID_949302,Human_RBP_ID_1678489,Human_RBP_ID_3968840,Human_RBP_ID_5152102,Human_RBP_ID_7593211,Human_RBP_ID_9400299,Human_RBP_ID_17663268,Human_RBP_ID_18413845,Human_RBP_ID_18472215,Human_RBP_ID_19016718,Human_RBP_ID_23067331,Human_RBP_ID_23116426,Human_RBP_ID_23120275,Human_RBP_ID_24548380,Human_RBP_ID_25997765,Human_RBP_ID_26353163,Human_RBP_ID_27827496 Human_Splice_Rec_755108,Human_Splice_Rec_755109,Human_Splice_Rec_755160,Human_Splice_Rec_755161,Human_Splice_Rec_755212,Human_Splice_Rec_755213,Human_Splice_Rec_755264,Human_Splice_Rec_755265,Human_Splice_Rec_755316,Human_Splice_Rec_755317 113850 RMVar_ID_113850 Human_SNP_ID_862821223 m1A Human chr6 - 111393671 111393671 111393671 AAAAAGAAGAAAGGTAGTTACTAGAGGCTGGGAAGGGTGTATGGGAAGGGTTCCAGGAAGATACG AAAAAGAAGAAAGGTAGTTACTAGAGGCTGGGGAGGGTGTATGGGAAGGGTTCCAGGAAGATACG T C REV3L Ensembl:ENSG00000009413 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111393633..111393716 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_57503,RMVar_hsa_circ_37796,RMVar_hsa_circ_75796,RMVar_hsa_circ_240955,RMVar_hsa_circ_240959,RMVar_hsa_circ_83332,RMVar_hsa_circ_77645,RMVar_hsa_circ_240969,RMVar_hsa_circ_44003,RMVar_hsa_circ_376655,RMVar_hsa_circ_8297,RMVar_hsa_circ_240979,RMVar_hsa_circ_28577,RMVar_hsa_circ_73262,RMVar_hsa_circ_4368,RMVar_hsa_circ_93025,RMVar_hsa_circ_295421,RMVar_hsa_circ_240981,RMVar_hsa_circ_240982,RMVar_hsa_circ_330062,RMVar_hsa_circ_240983,RMVar_hsa_circ_327674,RMVar_hsa_circ_290471,RMVar_hsa_circ_272425,RMVar_hsa_circ_240987,RMVar_hsa_circ_240989,RMVar_hsa_circ_240990,RMVar_hsa_circ_240991,RMVar_hsa_circ_240988,RMVar_hsa_circ_240986,RMVar_hsa_circ_323832,RMVar_hsa_circ_329514,RMVar_hsa_circ_278651,RMVar_hsa_circ_240996,RMVar_hsa_circ_240992,RMVar_hsa_circ_240993,RMVar_hsa_circ_283790,RMVar_hsa_circ_303911,RMVar_hsa_circ_240994,RMVar_hsa_circ_295409,RMVar_hsa_circ_240995 113851 RMVar_ID_113851 Human_SNP_ID_862827967 m1A Human chr6 + 112081172 112081172 112081172 AATACATCTCTCAGTGGTCCCTGCAGAATTTCATTCACTACCCCTTCTTCCATATCAATCAAGAC AATACATCTCTCAGTGGTCCCTGCAGAATTTCCTTCACTACCCCTTCTTCCATATCAATCAAGAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:112081049..112081246 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 113852 RMVar_ID_113852 Human_SNP_ID_862844796 m1A Human chr6 - 31271133 31271133 31271133 CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCACGTGCGTGGAGTGGCTCCGCAGATACCTGGAG CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCCCGTGCGTGGAGTGGCTCCGCAGATACCTGGAG T G HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31271076..31271175 26863196 MeRIP-seq:(Medium) rs1050685 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,pancreas ductal_carcinoma,COCA,mouth squamous_cell_carcinoma,skin basal_cell_carcinoma,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 74 biliary tract,gallbladder,pancreas,skin,head and neck,large intestine Human_RBP_ID_252636,Human_RBP_ID_661253,Human_RBP_ID_791391,Human_RBP_ID_4880719,Human_RBP_ID_17663600,Human_RBP_ID_22461056,Human_RBP_ID_22773381 Human_Splice_Rec_751687,Human_Splice_Rec_751701,Human_Splice_Rec_751715,Human_Splice_Rec_751729,Human_Splice_Rec_751743,Human_Splice_Rec_751755,Human_Splice_Rec_751759 113853 RMVar_ID_113853 Human_SNP_ID_862844806 m1A Human chr6 - 31271133 31271133 31271133 CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCACGTGCGTGGAGTGGCTCCGCAGATACCTGGAG CGGCGGAGCAGCTGAGAGCCTACCTGGAGGGCGCGTGCGTGGAGTGGCTCCGCAGATACCTGGAG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31271076..31271175 26863196 MeRIP-seq:(Medium) rs1050685 Functional Loss SNV ICGC,COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma,COCA,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 25 biliary tract,gallbladder,head and neck,large intestine Human_RBP_ID_252636,Human_RBP_ID_661253,Human_RBP_ID_791391,Human_RBP_ID_4880719,Human_RBP_ID_17663600,Human_RBP_ID_22461056,Human_RBP_ID_22773381 Human_Splice_Rec_751687,Human_Splice_Rec_751701,Human_Splice_Rec_751715,Human_Splice_Rec_751729,Human_Splice_Rec_751743,Human_Splice_Rec_751755,Human_Splice_Rec_751759 113854 RMVar_ID_113854 Human_SNP_ID_862881713 m1A Human chr6 + 13616453 13616453 13616453 TACATGACTTTCTATTAATTTTAAACGTTTTCATTCCAAAAGAAAAGAAAACTCCTTCCAGACAC TACATGACTTTCTATTAATTTTAAACGTTTTCGTTCCAAAAGAAAAGAAAACTCCTTCCAGACAC A G NOL7 Ensembl:ENSG00000225921 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:13616451..13616500 26863196 MeRIP-seq:(Medium) rs1255308642 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_22683696 Human_Splice_Rec_739583,Human_Splice_Rec_739597,Human_Splice_Rec_739603 RMVar_hsa_circ_55040 113855 RMVar_ID_113855 Human_SNP_ID_862913965 m1A Human chr6 + 26216995 26216995 26216995 TAGGAAGCCACTATGTCTGGACGTGGAAAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCG TAGGAAGCCACTATGTCTGGACGTGGAAAGCATGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCG A T H2AC8 Ensembl:ENSG00000277075 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26216976..26217000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney Human_RBP_ID_791812,Human_RBP_ID_22462474,Human_RBP_ID_23214688,Human_RBP_ID_24437165 113856 RMVar_ID_113856 Human_SNP_ID_862914291 m1A Human chr6 - 29944103 29944103 29944103 TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGAAAATTCAGGCATTTTGCATCTGTCATGGGACAC TGTCTTGGGGGGGTCTGACGGGAAGAGTCAGATAATTCAGGCATTTTGCATCTGTCATGGGACAC T A HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HeLa cell line,mRNA;HTR8/Svneo,Normoxia chr6:29944101..29944175 26863196,32194978 MeRIP-seq:(Medium) rs17885212 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine 113857 RMVar_ID_113857 Human_SNP_ID_862942768 m1A Human chr6 + 41789294 41789294 41789294 TGCGGGAGTTTGGCTGGCCAGGAACTTGAGTGACATTGACCTCATGGCACCTCAGCCAGGGGTGT TGCGGGAGTTTGGCTGGCCAGGAACTTGAGTGGCATTGACCTCATGGCACCTCAGCCAGGGGTGT A G AL365205.1,TOMM6 Ensembl:ENSG00000124593,Ensembl:ENSG00000214736 Protein coding,Protein coding 3'UTR,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_664472,Human_RBP_ID_951927,Human_RBP_ID_1069750,Human_RBP_ID_1673347,Human_RBP_ID_2021269,Human_RBP_ID_5121997,Human_RBP_ID_5151909,Human_RBP_ID_15825783,Human_RBP_ID_17307197,Human_RBP_ID_17663740,Human_RBP_ID_18171117,Human_RBP_ID_22460705,Human_RBP_ID_23215255,Human_RBP_ID_24162971,Human_RBP_ID_26536680,Human_RBP_ID_27347242 Human_Splice_Rec_769532,Human_Splice_Rec_769533,Human_Splice_Rec_769548,Human_Splice_Rec_769549,Human_Splice_Rec_769564,Human_Splice_Rec_769565,Human_Splice_Rec_769614,Human_Splice_Rec_769615,Human_Splice_Rec_769618,Human_Splice_Rec_769619 Human_miRNA_ID_2996114 RMVar_hsa_circ_96110,RMVar_hsa_circ_238321,RMVar_hsa_circ_114792,RMVar_hsa_circ_81070,RMVar_hsa_circ_238322,RMVar_hsa_circ_116733,RMVar_hsa_circ_100397,RMVar_hsa_circ_238323,RMVar_hsa_circ_238324,RMVar_hsa_circ_238325 113858 RMVar_ID_113858 Human_SNP_ID_862954942 m1A Human chr6 + 99521102 99521102 99521102 CCGCAATGGTGCTACCCTGGTTGCTGCTCGAGACTGCGCGCAGGGCGGTCCTCGGGTCCGCGGAG CCGCAATGGTGCTACCCTGGTTGCTGCTCGAGGCTGCGCGCAGGGCGGTCCTCGGGTCCGCGGAG A G TSTD3 Ensembl:ENSG00000279170 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:99521051..99521180 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia_therapy_related 2 haematopoietic and lymphoid tissue Human_RBP_ID_4904192,Human_RBP_ID_8652437,Human_RBP_ID_18425706,Human_RBP_ID_27827929 Human_Splice_Rec_797389,Human_Splice_Rec_797395,Human_Splice_Rec_797403,Human_Splice_Rec_797411,Human_Splice_Rec_797417,Human_Splice_Rec_797423 113859 RMVar_ID_113859 Human_SNP_ID_862955202 m1A Human chr6 + 20716401 20716401 20716401 AGTTTGTGAAGAGCTGGGGAATGAGATTTTTTAAAATTATCCTGCTGTTGGACAGAAAGTACAGC AGTTTGTGAAGAGCTGGGGAATGAGATTTTTTTAAATTATCCTGCTGTTGGACAGAAAGTACAGC A T CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20716397..20716486 26863196 MeRIP-seq:(Medium) rs1217821385 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 113860 RMVar_ID_113860 Human_SNP_ID_862961952 m1A Human chr6 + 34606844 34606844 34606844 GCTGTGTGTTGAACTCCGTTTCAAAAGATGACAGCTGCTGCGTTACTCCTAAAAGTCCACCCACC GCTGTGTGTTGAACTCCGTTTCAAAAGATGACGGCTGCTGCGTTACTCCTAAAAGTCCACCCACC A G RF00017-4751 RNACentral:URS000099F4EE SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34606793..34606896 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113861 RMVar_ID_113861 Human_SNP_ID_862962796 m1A Human chr6 - 130956045 130956045 130956045 CAAGAGATTAAAGTTGAAGTCAAGGAAGAAAAACCCTCAGTGAGCAAGGAAGAAAAACCCTCAGT CAAGAGATTAAAGTTGAAGTCAAGGAAGAAAACCCCTCAGTGAGCAAGGAAGAAAAACCCTCAGT T G EPB41L2 Ensembl:ENSG00000079819 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:130955974..130956167 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 12 large intestine Human_RBP_ID_215504,Human_RBP_ID_950034,Human_RBP_ID_2008465,Human_RBP_ID_18854209,Human_RBP_ID_24548628,Human_RBP_ID_26354379 Human_Splice_Rec_810407,Human_Splice_Rec_810439,Human_Splice_Rec_810473,Human_Splice_Rec_810511,Human_Splice_Rec_810543,Human_Splice_Rec_810593,Human_Splice_Rec_810621,Human_Splice_Rec_810659,Human_Splice_Rec_810709,Human_Splice_Rec_810743,Human_Splice_Rec_810769,Human_Splice_Rec_810799,Human_Splice_Rec_810883,Human_Splice_Rec_810937 RMVar_hsa_circ_64254,RMVar_hsa_circ_62474,RMVar_hsa_circ_328987,RMVar_hsa_circ_58482,RMVar_hsa_circ_75440,RMVar_hsa_circ_241493,RMVar_hsa_circ_268381,RMVar_hsa_circ_69133,RMVar_hsa_circ_301543,RMVar_hsa_circ_241492,RMVar_hsa_circ_306710 113862 RMVar_ID_113862 Human_SNP_ID_862967646 m1A Human chr6 + 73518263 73518263 73518263 CGCTTATTTGGCCTGGATGGTTCAGGATAATCACCTTGGAAAAAAGATTTGCATTCAGTGCAAAT CGCTTATTTGGCCTGGATGGTTCAGGATAATCGCCTTGGAAAAAAGATTTGCATTCAGTGCAAAT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:73518225..73518377 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 113863 RMVar_ID_113863 Human_SNP_ID_862971112 m1A Human chr6 - 42890765 42890765 42890765 CGACCCGACATGGAGCGTCCCCGCAGTCCCCAATGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT CGACCCGACATGGAGCGTCCCCGCAGTCCCCAGTGCTCGGCCCCGGCCTCTGCCTCAGCTTCGGT T C C6orf226 Ensembl:ENSG00000221821 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:42890671..42890793 26863196 MeRIP-seq:(Medium) rs370729479 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_4890228,Human_RBP_ID_5511728 Human_miRNA_ID_694383 113864 RMVar_ID_113864 Human_SNP_ID_862974283 m1A Human chr6 + 120262375 120262375 120262375 CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGAAGGGCCAGCGCCATTCCAATGGAATGGCTTTTT CAGTTGAACGTGTGTCAGTCAGTCCTGAGAGATGGGCCAGCGCCATTCCAATGGAATGGCTTTTT A T - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:120262326..120262400 26863196 MeRIP-seq:(Medium) rs200378569 Functional Loss SNV ICGC 33..33 33 COCA 1 - 113865 RMVar_ID_113865 Human_SNP_ID_863005970 m1A Human chr6 - 151350096 151350096 151350096 CAGACACGTGATCTCCTCGGGCTCCTCAGGGGATGAGGCAGAGCTCTCGCCCTTTTGCTCCTCCT CAGACACGTGATCTCCTCGGGCTCCTCAGGGGGTGAGGCAGAGCTCTCGCCCTTTTGCTCCTCCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:151349990..151350140 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 113866 RMVar_ID_113866 Human_SNP_ID_863013621 m1A Human chr6 + 148390183 148390183 148390183 CATCGATGACCTGGCGCAGCAGTATGCAGATTATTACAACACCTGTTTCTCCGACGTGTGCGAGA CATCGATGACCTGGCGCAGCAGTATGCAGATTTTTACAACACCTGTTTCTCCGACGTGTGCGAGA A T SASH1 Ensembl:ENSG00000111961 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:148390097..148390203 26863196 MeRIP-seq:(Medium) rs1562373828 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4868183 Human_Splice_Rec_821670,Human_Splice_Rec_821671,Human_Splice_Rec_821676,Human_Splice_Rec_821677 Human_miRNA_ID_2889900 RMVar_hsa_circ_7257,RMVar_hsa_circ_100413,RMVar_hsa_circ_299914,RMVar_hsa_circ_334986,RMVar_hsa_circ_21665,RMVar_hsa_circ_242143,RMVar_hsa_circ_242145,RMVar_hsa_circ_242146,RMVar_hsa_circ_242144 113867 RMVar_ID_113867 Human_SNP_ID_863035558 m1A Human chr6 - 43501594 43501594 43501594 GGCAGTCCTGCCCAATTTCCAGCTCACGTTCCAGGGCCTCAGTGCGTCTGGTGGCGGAGGCCAGG GGCAGTCCTGCCCAATTTCCAGCTCACGTTCCGGGGCCTCAGTGCGTCTGGTGGCGGAGGCCAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43501501..43501607 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113868 RMVar_ID_113868 Human_SNP_ID_863043366 m1A Human chr6 - 26056338 26056338 26056338 TAAAGAAGAAGGCGGCCAAAAAGGCTGGGGGTACGCCTCGTAAGGCGTCTGGTCCCCCGGTGTCA TAAAGAAGAAGGCGGCCAAAAAGGCTGGGGGTCCGCCTCGTAAGGCGTCTGGTCCCCCGGTGTCA T G H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26056287..26056475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue Human_RBP_ID_658986,Human_RBP_ID_1045990,Human_RBP_ID_1668818,Human_RBP_ID_3804152,Human_RBP_ID_4876080,Human_RBP_ID_5511040,Human_RBP_ID_7585593,Human_RBP_ID_8269812,Human_RBP_ID_8639979,Human_RBP_ID_8899087,Human_RBP_ID_9335985,Human_RBP_ID_9400067,Human_RBP_ID_15770019,Human_RBP_ID_18071324,Human_RBP_ID_18211348,Human_RBP_ID_18449931,Human_RBP_ID_22309192,Human_RBP_ID_22460435,Human_RBP_ID_22830337,Human_RBP_ID_24153223,Human_RBP_ID_26353478,Human_RBP_ID_26534361,Human_RBP_ID_26714192,Human_RBP_ID_27093642,Human_RBP_ID_27343948,Human_RBP_ID_27521861,Human_RBP_ID_27753980 113869 RMVar_ID_113869 Human_SNP_ID_863056195 m1A Human chr6 - 18258402 18258402 18258402 TAATTAAGAAATACTAAATTAATTTCTAGAAAAGAGTCTCATCGTGGAAGGCAAGAGGGAAAAGA TAATTAAGAAATACTAAATTAATTTCTAGAAATGAGTCTCATCGTGGAAGGCAAGAGGGAAAAGA T A DEK Ensembl:ENSG00000124795 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:18258351..18258425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_658313,Human_RBP_ID_792139,Human_RBP_ID_2015727,Human_RBP_ID_2997433,Human_RBP_ID_7579424,Human_RBP_ID_9400004,Human_RBP_ID_15754094,Human_RBP_ID_17663222,Human_RBP_ID_23116418,Human_RBP_ID_24150816,Human_RBP_ID_24548544,Human_RBP_ID_26353441,Human_RBP_ID_27827350 Human_Splice_Rec_741184,Human_Splice_Rec_741185,Human_Splice_Rec_741210,Human_Splice_Rec_741211,Human_Splice_Rec_741224,Human_Splice_Rec_741225,Human_Splice_Rec_741244,Human_Splice_Rec_741245,Human_Splice_Rec_741266,Human_Splice_Rec_741267,Human_Splice_Rec_741284,Human_Splice_Rec_741285,Human_Splice_Rec_741322,Human_Splice_Rec_741323,Human_Splice_Rec_741346,Human_Splice_Rec_741347,Human_Splice_Rec_741356,Human_Splice_Rec_741357 RMVar_hsa_circ_62800,RMVar_hsa_circ_358479,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,RMVar_hsa_circ_65487,RMVar_hsa_circ_317221,RMVar_hsa_circ_283292,RMVar_hsa_circ_237485,RMVar_hsa_circ_64068,RMVar_hsa_circ_27303,RMVar_hsa_circ_237486,RMVar_hsa_circ_237487,RMVar_hsa_circ_68404,RMVar_hsa_circ_272868,RMVar_hsa_circ_237488,RMVar_hsa_circ_296652,RMVar_hsa_circ_361870 113870 RMVar_ID_113870 Human_SNP_ID_863065240 m1A Human chr6 - 159711879 159711879 159711879 TCAGAGCAATGTGAGTGGTGGTTATGGAGATCAGAGCAGTGTGACTGGTGGTTATGGAGGTGGTT TCAGAGCAATGTGAGTGGTGGTTATGGAGATCTGAGCAGTGTGACTGGTGGTTATGGAGGTGGTT T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:159711825..159711910 26863196 MeRIP-seq:(Medium) rs1282884202 Functional Loss SNV COSMIC 33..33 33 arm Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 1 skin,upper extremity Human_RBP_ID_840327,Human_RBP_ID_24144691 113871 RMVar_ID_113871 Human_SNP_ID_863068874 m1A Human chr6 + 26251700 26251700 26251700 GTCCGCTCCCGCCCCGAAGAAGGGCTCCAAGAAGGCGGTGACCAAGGCGCAGAAGAAGGATGGCA GTCCGCTCCCGCCCCGAAGAAGGGCTCCAAGACGGCGGTGACCAAGGCGCAGAAGAAGGATGGCA A C H2BC9 Ensembl:ENSG00000275713 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:26251676..26251700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 1 oesophagus Human_RBP_ID_5478665,Human_RBP_ID_22461696,Human_RBP_ID_22706110,Human_RBP_ID_26353496,Human_RBP_ID_26828013 113872 RMVar_ID_113872 Human_SNP_ID_863072489 m1A Human chr6 - 33414270 33414270 33414270 AAGTATTTCTTCTTACAGCAAACACTGAGGTGATACAGGACAAGATGGGCCACATCCACCCTGGA AAGTATTTCTTCTTACAGCAAACACTGAGGTGGTACAGGACAAGATGGGCCACATCCACCCTGGA T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33414251..33414300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 113873 RMVar_ID_113873 Human_SNP_ID_863077240 m1A Human chr6 + 43132099 43132099 43132099 GACCCAGGTCCGGCCACGCAATGCAGGGATCTACCGCTGCATTGGCCAGGGGCAGAGGGGCCCAC GACCCAGGTCCGGCCACGCAATGCAGGGATCTGCCGCTGCATTGGCCAGGGGCAGAGGGGCCCAC A G PTK7 Ensembl:ENSG00000112655 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43132051..43132150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_4890842,Human_RBP_ID_22461285,Human_RBP_ID_22773620 Human_Splice_Rec_771664,Human_Splice_Rec_771665,Human_Splice_Rec_771700,Human_Splice_Rec_771701,Human_Splice_Rec_771738,Human_Splice_Rec_771739,Human_Splice_Rec_771750,Human_Splice_Rec_771751,Human_Splice_Rec_771782,Human_Splice_Rec_771783,Human_Splice_Rec_771816,Human_Splice_Rec_771817,Human_Splice_Rec_771852,Human_Splice_Rec_771853,Human_Splice_Rec_771888,Human_Splice_Rec_771889,Human_Splice_Rec_771924,Human_Splice_Rec_771925,Human_Splice_Rec_771954,Human_Splice_Rec_771955,Human_Splice_Rec_771961 RMVar_hsa_circ_3385,RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_84927,RMVar_hsa_circ_99302,RMVar_hsa_circ_316233,RMVar_hsa_circ_238560,RMVar_hsa_circ_323586,RMVar_hsa_circ_238562,RMVar_hsa_circ_238563,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_90656,RMVar_hsa_circ_110599,RMVar_hsa_circ_238566,RMVar_hsa_circ_238567 113874 RMVar_ID_113874 Human_SNP_ID_863081796 m1A Human chr6 + 44250429 44250429 44250429 ATGTGGGTTCAGATGAGGAGGATGACAGCGGTAAGGATAAGAAGAAGAAAACTAAGAAGATCAAA ATGTGGGTTCAGATGAGGAGGATGACAGCGGTGAGGATAAGAAGAAGAAAACTAAGAAGATCAAA A G HSP90AB1 Ensembl:ENSG00000096384 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:44250276..44250550 32194978 MeRIP-seq:(Medium) rs1252188086 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver Human_RBP_ID_79143,Human_RBP_ID_214902,Human_RBP_ID_251200,Human_RBP_ID_665452,Human_RBP_ID_841790,Human_RBP_ID_947761,Human_RBP_ID_1047899,Human_RBP_ID_1674066,Human_RBP_ID_2022055,Human_RBP_ID_3008782,Human_RBP_ID_3810241,Human_RBP_ID_7609850,Human_RBP_ID_8270185,Human_RBP_ID_8646013,Human_RBP_ID_8901807,Human_RBP_ID_9194860,Human_RBP_ID_9400616,Human_RBP_ID_15836318,Human_RBP_ID_17536380,Human_RBP_ID_17671993,Human_RBP_ID_18413856,Human_RBP_ID_18539131,Human_RBP_ID_18866657,Human_RBP_ID_19129471,Human_RBP_ID_22010805,Human_RBP_ID_22106854,Human_RBP_ID_22773666,Human_RBP_ID_23067586,Human_RBP_ID_23116467,Human_RBP_ID_24164505,Human_RBP_ID_24548403,Human_RBP_ID_26353199,Human_RBP_ID_27827715 RMVar_hsa_circ_87341,RMVar_hsa_circ_112737,RMVar_hsa_circ_339826,RMVar_hsa_circ_97879,RMVar_hsa_circ_238764,RMVar_hsa_circ_364132,RMVar_hsa_circ_238765,RMVar_hsa_circ_111784,RMVar_hsa_circ_238767,RMVar_hsa_circ_238769,RMVar_hsa_circ_91196,RMVar_hsa_circ_238768,RMVar_hsa_circ_22290,RMVar_hsa_circ_118483,RMVar_hsa_circ_238771,RMVar_hsa_circ_375698,RMVar_hsa_circ_55721,RMVar_hsa_circ_238772 113875 RMVar_ID_113875 Human_SNP_ID_863101308 m1A Human chr6 - 4130454 4130454 4130454 GCCTGGAACAGACAGGAAATCAACTGGGTTTGAAACTCTGGTGGTGACCTCCGAAGATGGCATCA GCCTGGAACAGACAGGAAATCAACTGGGTTTGGAACTCTGGTGGTGACCTCCGAAGATGGCATCA T C ECI2 Ensembl:ENSG00000198721 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:4130351..4130575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_9194610,Human_RBP_ID_9399854,Human_RBP_ID_26006529,Human_RBP_ID_27828224 Human_Splice_Rec_734741,Human_Splice_Rec_734759,Human_Splice_Rec_734777,Human_Splice_Rec_734797,Human_Splice_Rec_734815,Human_Splice_Rec_734829,Human_Splice_Rec_734845,Human_Splice_Rec_734863,Human_Splice_Rec_734879,Human_Splice_Rec_734893 Human_miRNA_ID_499577 RMVar_hsa_circ_69854,RMVar_hsa_circ_69893 113876 RMVar_ID_113876 Human_SNP_ID_863107544 m1A Human chr6 - 132816998 132816998 132816998 TTACGGGGTTTCCCCTCTCTGTCAATTTTACAAAGGCCTACCCATTCTCCTAGTTTCTTGTTGTC TTACGGGGTTTCCCCTCTCTGTCAATTTTACAGAGGCCTACCCATTCTCCTAGTTTCTTGTTGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:132816551..132817050 32194978 MeRIP-seq:(Medium) rs767661348 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 1 lung 113877 RMVar_ID_113877 Human_SNP_ID_863112490 m1A Human chr6 + 133513021 133513021 133513021 TTACAGAAGAGTAAAAGAATTATATAACACCTACAAGAACAACGTTGGAGGTATGTGTGGCTTTT TTACAGAAGAGTAAAAGAATTATATAACACCTGCAAGAACAACGTTGGAGGTATGTGTGGCTTTT A G EYA4 Ensembl:ENSG00000112319 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:133512970..133513080 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 10 uterus Human_Splice_Rec_812765,Human_Splice_Rec_812799,Human_Splice_Rec_812837,Human_Splice_Rec_812875,Human_Splice_Rec_812915,Human_Splice_Rec_812953,Human_Splice_Rec_812989,Human_Splice_Rec_813024,Human_Splice_Rec_813066 RMVar_hsa_circ_15198,RMVar_hsa_circ_24433,RMVar_hsa_circ_241589,RMVar_hsa_circ_285190,RMVar_hsa_circ_20282,RMVar_hsa_circ_8003,RMVar_hsa_circ_67733,RMVar_hsa_circ_52908 113878 RMVar_ID_113878 Human_SNP_ID_863156434 m1A Human chr6 - 3226644 3226644 3226644 GTCTCAGTTTTGGGAGGTCATCAGTGATGAGCATGGGATTGACCCCACTGGCAGTTACCATGGAG GTCTCAGTTTTGGGAGGTCATCAGTGATGAGCTTGGGATTGACCCCACTGGCAGTTACCATGGAG T A TUBB2B Ensembl:ENSG00000137285 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:3226593..3227510 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_662123,Human_RBP_ID_4912292,Human_RBP_ID_22103198 Human_Splice_Rec_733988,Human_Splice_Rec_733989,Human_Splice_Rec_733993 RMVar_hsa_circ_236953 113879 RMVar_ID_113879 Human_SNP_ID_863164739 m1A Human chr6 + 34646675 34646675 34646675 CCTGATACATTCCTGCTCTGCTGGGGCTGCACATCTGGACGCTGACATCTGCAATCTCTTGGGGC CCTGATACATTCCTGCTCTGCTGGGGCTGCACCTCTGGACGCTGACATCTGCAATCTCTTGGGGC A C RF00017-4751 RNACentral:URS000099F4EE SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:34646625..34646721 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck 113880 RMVar_ID_113880 Human_SNP_ID_863199721 m1A Human chr6 - 17706843 17706843 17706843 CGGCGGCGGAGGCTGCAGGGACGACGACGACGACGGCGGCGGGGCGGGCGCTGTGCGCACAGGGG CGGCGGCGGAGGCTGCAGGGACGACGACGACGGCGGCGGCGGGGCGGGCGCTGTGCGCACAGGGG T C NUP153 Ensembl:ENSG00000124789 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:17706546..17706899 26863196 MeRIP-seq:(Medium) rs963701919 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_4874413 113881 RMVar_ID_113881 Human_SNP_ID_863206539 m1A Human chr6 + 27139441 27139441 27139441 CCATTCGGCGCCTTGCTCGCCGCGGCGGCGTGAAGCGCATTTCTGGCCTCATCTATGAGGAGACC CCATTCGGCGCCTTGCTCGCCGCGGCGGCGTGCAGCGCATTTCTGGCCTCATCTATGAGGAGACC A C H4C9 Ensembl:ENSG00000276180 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:27139301..27139561;chr6:27139276..27139475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_9336520,Human_RBP_ID_22462499,Human_RBP_ID_22773025 RMVar_hsa_circ_122237,RMVar_hsa_circ_237769 113882 RMVar_ID_113882 Human_SNP_ID_863226858 m1A Human chr6 - 33292162 33292162 33292162 TCTGCCTCAGGAACTCCTCCGAGTGAGGGAGGAGGGGGCTCCTTTCCCAGGATCAAGGCCACAGG TCTGCCTCAGGAACTCCTCCGAGTGAGGGAGGGGGGGGCTCCTTTCCCAGGATCAAGGCCACAGG T C RGL2 Ensembl:ENSG00000237441 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:33292052..33292203 32194978 MeRIP-seq:(Medium) rs750533431 Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 2 lung Human_RBP_ID_18171262 113883 RMVar_ID_113883 Human_SNP_ID_863229290 m1A Human chr6 - 31829999 31829999 31829999 AAATAATGAAGCCAGCTAATTACCATCAGGTTACAACTTTACAAAGAAGTGAAGCAGCAAAGAGC AAATAATGAAGCCAGCTAATTACCATCAGGTTTCAACTTTACAAAGAAGTGAAGCAGCAAAGAGC T A RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31829776..31830025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113884 RMVar_ID_113884 Human_SNP_ID_863231387 m1A Human chr6 - 105179996 105179996 105179996 CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGAGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC CGGCACCCGCCCGCGCCGCCGCGCCGCTCCGGCGCCCGCTGCGGTCACGCTGCGCCCGGCGCCGC T G POPDC3 Ensembl:ENSG00000132429 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:105179895..105179995 26863410 MeRIP-seq:(Medium) rs1365044018 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113885 RMVar_ID_113885 Human_SNP_ID_863258623 m1A Human chr6 + 26158243 26158243 26158243 CTCCAAGAAGGCGGTGACTAAGGCTCAGAAGAAGGACGGGAAGAAGCGCAAGCGCAGCCGCAAGG CTCCAAGAAGGCGGTGACTAAGGCTCAGAAGATGGACGGGAAGAAGCGCAAGCGCAGCCGCAAGG A T H2BC5 Ensembl:ENSG00000158373 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26158193..26158388 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 2 pancreas Human_RBP_ID_81820,Human_RBP_ID_252340,Human_RBP_ID_1668890,Human_RBP_ID_2016714,Human_RBP_ID_3000952,Human_RBP_ID_3804210,Human_RBP_ID_4876151,Human_RBP_ID_5428204,Human_RBP_ID_5617696,Human_RBP_ID_7585717,Human_RBP_ID_8640055,Human_RBP_ID_8899142,Human_RBP_ID_9335995,Human_RBP_ID_9400082,Human_RBP_ID_15770232,Human_RBP_ID_17710134,Human_RBP_ID_18538975,Human_RBP_ID_18860626,Human_RBP_ID_22460455,Human_RBP_ID_22830385,Human_RBP_ID_26353125,Human_RBP_ID_26534445,Human_RBP_ID_26714218,Human_RBP_ID_27093680,Human_RBP_ID_27343987,Human_RBP_ID_27521922 113886 RMVar_ID_113886 Human_SNP_ID_863268387 m1A Human chr6 + 31536471 31536471 31536471 CATCATTTGGCTCCAAAGAACAACTCCCCAGCATTAGCCAAGCCCCAGCACTGCCACTCACCGAG CATCATTTGGCTCCAAAGAACAACTCCCCAGCGTTAGCCAAGCCCCAGCACTGCCACTCACCGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31536469..31536691 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113887 RMVar_ID_113887 Human_SNP_ID_863276255 m1A Human chr6 - 31410702 31410702 31410702 CCCTGGTCTCTCTGTCCCATGTCTTATTTCCCAGGACATCTTCTGCCCACTGTCCCTGGGGCTTT CCCTGGTCTCTCTGTCCCATGTCTTATTTCCCTGGACATCTTCTGCCCACTGTCCCTGGGGCTTT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:31410620..31410983 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113888 RMVar_ID_113888 Human_SNP_ID_863291354 m1A Human chr6 - 158789371 158789371 158789371 TTAAGCGTAATTTGTTTCATTCTGTTTTTCAGATCAATGTCCGAGTTACCACCATGGATGCAGAG TTAAGCGTAATTTGTTTCATTCTGTTTTTCAGGTCAATGTCCGAGTTACCACCATGGATGCAGAG T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158789326..158789429 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_79086,Human_RBP_ID_25980533,Human_RBP_ID_26830034 Human_Splice_Rec_828620,Human_Splice_Rec_828621,Human_Splice_Rec_828641,Human_Splice_Rec_828664,Human_Splice_Rec_828665,Human_Splice_Rec_828688,Human_Splice_Rec_828689 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_125699,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_242786,RMVar_hsa_circ_298659,RMVar_hsa_circ_332275,RMVar_hsa_circ_19359,RMVar_hsa_circ_110280,RMVar_hsa_circ_242788,RMVar_hsa_circ_46193,RMVar_hsa_circ_242789 113889 RMVar_ID_113889 Human_SNP_ID_863309678 m1A Human chr6 - 165955408 165955408 165955408 AGCAAATAAGGGACCAGTCACTTCCACGTTTCAGGAAGCCTCATCTGGAAATTGTTGGAGAAACA AGCAAATAAGGGACCAGTCACTTCCACGTTTCTGGAAGCCTCATCTGGAAATTGTTGGAGAAACA T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:165955276..165955500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2992918,Human_RBP_ID_15729493 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 113890 RMVar_ID_113890 Human_SNP_ID_863315994 m1A Human chr6 - 27251806 27251806 27251806 AGCTCCGTCCGCAATGCTGCTTGAGCCGCCCCACCCGAGCGCAGCCGCCGCTCCACTTCAGCGAA AGCTCCGTCCGCAATGCTGCTTGAGCCGCCCCCCCCGAGCGCAGCCGCCGCTCCACTTCAGCGAA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27251557..27251931 26863196 MeRIP-seq:(Medium) rs578258212 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113891 RMVar_ID_113891 Human_SNP_ID_863324804 m1A Human chr6 + 43446359 43446359 43446359 TTGCCACCAGTGCCACAATGCAGTGGCTGGACATTCGGCTACAGCTCATGGGGGCGGCAGTGGTC TTGCCACCAGTGCCACAATGCAGTGGCTGGACTTTCGGCTACAGCTCATGGGGGCGGCAGTGGTC A T ABCC10 Ensembl:ENSG00000124574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43446309..43446868 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5532472,Human_RBP_ID_22772758 Human_Splice_Rec_772674,Human_Splice_Rec_772675,Human_Splice_Rec_772722,Human_Splice_Rec_772723,Human_Splice_Rec_772752,Human_Splice_Rec_772753 Human_miRNA_ID_2893790 RMVar_hsa_circ_64130,RMVar_hsa_circ_238615,RMVar_hsa_circ_117997,RMVar_hsa_circ_101309,RMVar_hsa_circ_238614,RMVar_hsa_circ_372932,RMVar_hsa_circ_49177,RMVar_hsa_circ_238617,RMVar_hsa_circ_108013,RMVar_hsa_circ_238619 113892 RMVar_ID_113892 Human_SNP_ID_863330678 m1A Human chr6 - 27251256 27251256 27251256 CTCGGACTAGGCCCCACCTCCTACCTCCAGGGACCCGCCGATCGCGGTGCTCATTAGGCTTCGGG CTCGGACTAGGCCCCACCTCCTACCTCCAGGGCCCCGCCGATCGCGGTGCTCATTAGGCTTCGGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:27251208..27251546 26863196 MeRIP-seq:(Medium) rs773318984 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113893 RMVar_ID_113893 Human_SNP_ID_863332305 m1A Human chr6 - 33416680 33416680 33416680 TACCTGCAGTGGGTGCGCCAGGTCACAGAGTCAGTTTCTGACTCTATCACAGTCCTGCCATGATG TACCTGCAGTGGGTGCGCCAGGTCACAGAGTCGGTTTCTGACTCTATCACAGTCCTGCCATGATG T C CUTA Ensembl:ENSG00000112514 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA,LICA 2 - Human_RBP_ID_251290,Human_RBP_ID_662608,Human_RBP_ID_789478,Human_RBP_ID_1671844,Human_RBP_ID_5121950,Human_RBP_ID_5151871,Human_RBP_ID_8643090,Human_RBP_ID_9193702,Human_RBP_ID_17663126,Human_RBP_ID_22460663,Human_RBP_ID_22772738,Human_RBP_ID_27097088,Human_RBP_ID_27346263 Human_Splice_Rec_761918,Human_Splice_Rec_761928,Human_Splice_Rec_761934,Human_Splice_Rec_761942,Human_Splice_Rec_761952,Human_Splice_Rec_761962,Human_Splice_Rec_761972,Human_Splice_Rec_761982,Human_Splice_Rec_761992,Human_Splice_Rec_762002,Human_Splice_Rec_762008,Human_Splice_Rec_762016,Human_Splice_Rec_762028 Human_miRNA_ID_2453652,Human_miRNA_ID_2453653,Human_miRNA_ID_2453654 RMVar_hsa_circ_76578,RMVar_hsa_circ_95957,RMVar_hsa_circ_112562,RMVar_hsa_circ_237862,RMVar_hsa_circ_237863,RMVar_hsa_circ_237864 113894 RMVar_ID_113894 Human_SNP_ID_863350440 m1A Human chr6 - 78990959 78990959 78990959 TTTCAGTAGGCAAGAAGAATGGAGAACTGCAAAGGGAGAAGAAGAAATAAAGACTTACAGGTCAG TTTCAGTAGGCAAGAAGAATGGAGAACTGCAAGGGGAGAAGAAGAAATAAAGACTTACAGGTCAG T C PHIP Ensembl:ENSG00000146247 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:78990834..78991051 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus Human_RBP_ID_80500,Human_RBP_ID_949841,Human_RBP_ID_2026911,Human_RBP_ID_5618191,Human_RBP_ID_7631000,Human_RBP_ID_9400868,Human_RBP_ID_18413865,Human_RBP_ID_23067405,Human_RBP_ID_24548438,Human_RBP_ID_26049391,Human_RBP_ID_26355363,Human_RBP_ID_27827828 Human_Splice_Rec_789470,Human_Splice_Rec_789471 Human_miRNA_ID_545591,Human_miRNA_ID_580828,Human_miRNA_ID_2192770,Human_miRNA_ID_2206978 RMVar_hsa_circ_731,RMVar_hsa_circ_38104,RMVar_hsa_circ_119691,RMVar_hsa_circ_239720,RMVar_hsa_circ_83904,RMVar_hsa_circ_239722,RMVar_hsa_circ_104838,RMVar_hsa_circ_95288,RMVar_hsa_circ_239726,RMVar_hsa_circ_239727,RMVar_hsa_circ_123535,RMVar_hsa_circ_87820,RMVar_hsa_circ_239728,RMVar_hsa_circ_266935,RMVar_hsa_circ_239729,RMVar_hsa_circ_373368,RMVar_hsa_circ_40827,RMVar_hsa_circ_49114,RMVar_hsa_circ_49870,RMVar_hsa_circ_42307,RMVar_hsa_circ_34712,RMVar_hsa_circ_8679,RMVar_hsa_circ_28489,RMVar_hsa_circ_19597,RMVar_hsa_circ_122781,RMVar_hsa_circ_239732,RMVar_hsa_circ_335412,RMVar_hsa_circ_361991,RMVar_hsa_circ_52827,RMVar_hsa_circ_239733,RMVar_hsa_circ_115427,RMVar_hsa_circ_61054,RMVar_hsa_circ_239736,RMVar_hsa_circ_84810,RMVar_hsa_circ_351299,RMVar_hsa_circ_376389,RMVar_hsa_circ_266050,RMVar_hsa_circ_62044,RMVar_hsa_circ_239742,RMVar_hsa_circ_239739,RMVar_hsa_circ_239738,RMVar_hsa_circ_77271,RMVar_hsa_circ_377117,RMVar_hsa_circ_239740,RMVar_hsa_circ_239741,RMVar_hsa_circ_83575,RMVar_hsa_circ_46514,RMVar_hsa_circ_74627,RMVar_hsa_circ_329594,RMVar_hsa_circ_359576,RMVar_hsa_circ_366533,RMVar_hsa_circ_267979,RMVar_hsa_circ_60423,RMVar_hsa_circ_38507,RMVar_hsa_circ_44898,RMVar_hsa_circ_71739,RMVar_hsa_circ_335187,RMVar_hsa_circ_18950,RMVar_hsa_circ_99204,RMVar_hsa_circ_239743,RMVar_hsa_circ_100333,RMVar_hsa_circ_367740,RMVar_hsa_circ_376718,RMVar_hsa_circ_314083,RMVar_hsa_circ_78432,RMVar_hsa_circ_60246,RMVar_hsa_circ_239744,RMVar_hsa_circ_239745,RMVar_hsa_circ_239746,RMVar_hsa_circ_94595,RMVar_hsa_circ_305761,RMVar_hsa_circ_239747 113895 RMVar_ID_113895 Human_SNP_ID_863401412 m1A Human chr6 - 26285362 26285362 26285362 CGGCGCCTTGCTCGTCGCGGCGGTGTCAAGCGAATTTCTGGCCTTATCTATGAGGAGACTCGTGG CGGCGCCTTGCTCGTCGCGGCGGTGTCAAGCGCATTTCTGGCCTTATCTATGAGGAGACTCGTGG T G H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr6:26285312..26285540;chr6:26285313..26285525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_1046113,Human_RBP_ID_1326476,Human_RBP_ID_1668995,Human_RBP_ID_2016774,Human_RBP_ID_3804296,Human_RBP_ID_4876438,Human_RBP_ID_7586022,Human_RBP_ID_8640146,Human_RBP_ID_8899189,Human_RBP_ID_9336005,Human_RBP_ID_15770525,Human_RBP_ID_17306023,Human_RBP_ID_17535179,Human_RBP_ID_18071500,Human_RBP_ID_18860708,Human_RBP_ID_22309336,Human_RBP_ID_22460489,Human_RBP_ID_22773296,Human_RBP_ID_23137943,Human_RBP_ID_24153440,Human_RBP_ID_26534540,Human_RBP_ID_26828018,Human_RBP_ID_27344070,Human_RBP_ID_27754056 113896 RMVar_ID_113896 Human_SNP_ID_863419127 m1A Human chr6 + 44109314 44109312 44109314 GAGCAAGGACACTGAGGAGGCTGCGCACGGGGAGGTTGGAGCGGAACGGCCTTGGGCTCCCACCT GAGCAAGGACACTGAGGAGGCTGCGCACGGAAGGGTTGGAGCGGAACGGCCTTGGGCTCCCACCT GGA AAG - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:44109205..44109348 26863196 MeRIP-seq:(Medium) - Functional Loss MNV ICGC 31..33 33 MELA 1 - 113897 RMVar_ID_113897 Human_SNP_ID_863447609 m1A Human chr6 + 42888234 42888234 42888234 TGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC TGGAGCGCAGTGGCATGATCTCAGCTCATTGCGGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1167593296 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 113898 RMVar_ID_113898 Human_SNP_ID_863456386 m1A Human chr6 + 31880784 31880784 31880784 AGACCCGGACGGGAATGATGTTGGGGTCACACAGGTGGTTGATGAAGCGGCTGATGTTGCCATAG AGACCCGGACGGGAATGATGTTGGGGTCACACGGGTGGTTGATGAAGCGGCTGATGTTGCCATAG A G EHMT2-AS1 Ensembl:ENSG00000237080 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31880735..31880831 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_755041 113899 RMVar_ID_113899 Human_SNP_ID_863465855 m1A Human chr6 + 73517933 73517933 73517933 ACTGTCTGTCTCATATCACGAACAGCAAAGCGACCTATTAAAAAAAAAGTTAATTATTACCCAAA ACTGTCTGTCTCATATCACGAACAGCAAAGCGCCCTATTAAAAAAAAAGTTAATTATTACCCAAA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:73517852..73518052 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113900 RMVar_ID_113900 Human_SNP_ID_863489810 m1A Human chr6 + 33391916 33391916 33391916 TACCCTGCTTCGCGAGCGGGCGAGAGAACGCGAGTCCCAGGATCCCCGGCACCCAGTTCTCTTCC TACCCTGCTTCGCGAGCGGGCGAGAGAACGCGGGTCCCAGGATCCCCGGCACCCAGTTCTCTTCC A G KIFC1 Ensembl:ENSG00000237649 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:33391901..33391925;chr6:33391851..33392111 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_4903933,Human_RBP_ID_7594604,Human_RBP_ID_22618231 Human_Splice_Rec_761711,Human_Splice_Rec_761731 113901 RMVar_ID_113901 Human_SNP_ID_863497785 m1A Human chr6 - 31815702 31815702 31815702 GCTCCGCTCTGAGATTGGGGGCTGGAAACGGAACACTGGATCCGCGAGAAGAGCTCGGTCCTTCC GCTCCGCTCTGAGATTGGGGGCTGGAAACGGAGCACTGGATCCGCGAGAAGAGCTCGGTCCTTCC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31815651..31815725 26863196 MeRIP-seq:(Medium) rs894889216 Functional Loss SNV TCGA,ICGC 33..33 33 READ,ESCA 2 - 113902 RMVar_ID_113902 Human_SNP_ID_863502500 m1A Human chr6 + 31729196 31729196 31729196 CATCCACACAGACTCCCCCTCCAACCGCTCGGATTTCTTAGTTTTCTTGTTTCTTCACCTGTCTG CATCCACACAGACTCCCCCTCCAACCGCTCGGCTTTCTTAGTTTTCTTGTTTCTTCACCTGTCTG A C RF00017-4498,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31728925..31729336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 113903 RMVar_ID_113903 Human_SNP_ID_863508257 m1A Human chr6 + 33676852 33676852 33676852 CGGAGCTGGACCGGCTGCGGACCATGGTGGAGAAGTCAGAGCTGTGGGTGGACAAGAAGGGCAGT CGGAGCTGGACCGGCTGCGGACCATGGTGGAGTAGTCAGAGCTGTGGGTGGACAAGAAGGGCAGT A T ITPR3 Ensembl:ENSG00000096433 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr6:33676801..33677027;chr6:33676801..33677024 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_841239,Human_RBP_ID_5622304,Human_RBP_ID_22746353,Human_RBP_ID_23215214 Human_Splice_Rec_762558,Human_Splice_Rec_762559,Human_Splice_Rec_762672,Human_Splice_Rec_762673 RMVar_hsa_circ_121196,RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_237873,RMVar_hsa_circ_103819,RMVar_hsa_circ_237875,RMVar_hsa_circ_126349,RMVar_hsa_circ_116868,RMVar_hsa_circ_115659,RMVar_hsa_circ_104279,RMVar_hsa_circ_237882,RMVar_hsa_circ_237880,RMVar_hsa_circ_237881,RMVar_hsa_circ_237879,RMVar_hsa_circ_119473,RMVar_hsa_circ_124935,RMVar_hsa_circ_237886,RMVar_hsa_circ_237887,RMVar_hsa_circ_237889,RMVar_hsa_circ_106042,RMVar_hsa_circ_237888,RMVar_hsa_circ_127782,RMVar_hsa_circ_107920,RMVar_hsa_circ_80690,RMVar_hsa_circ_86918,RMVar_hsa_circ_117273,RMVar_hsa_circ_237891,RMVar_hsa_circ_237892,RMVar_hsa_circ_100169,RMVar_hsa_circ_237895,RMVar_hsa_circ_117480,RMVar_hsa_circ_237897,RMVar_hsa_circ_237899,RMVar_hsa_circ_76223,RMVar_hsa_circ_237898,RMVar_hsa_circ_112834,RMVar_hsa_circ_237900,RMVar_hsa_circ_122562,RMVar_hsa_circ_108529,RMVar_hsa_circ_237904,RMVar_hsa_circ_93437,RMVar_hsa_circ_102430,RMVar_hsa_circ_237906,RMVar_hsa_circ_237905,RMVar_hsa_circ_237902,RMVar_hsa_circ_237903,RMVar_hsa_circ_237901,RMVar_hsa_circ_237910,RMVar_hsa_circ_102196,RMVar_hsa_circ_113711,RMVar_hsa_circ_123707,RMVar_hsa_circ_120798,RMVar_hsa_circ_104953,RMVar_hsa_circ_237912,RMVar_hsa_circ_237913,RMVar_hsa_circ_237914,RMVar_hsa_circ_237911,RMVar_hsa_circ_40363,RMVar_hsa_circ_95901,RMVar_hsa_circ_237915,RMVar_hsa_circ_93001,RMVar_hsa_circ_321243,RMVar_hsa_circ_112307,RMVar_hsa_circ_113192,RMVar_hsa_circ_237916,RMVar_hsa_circ_77443,RMVar_hsa_circ_237917,RMVar_hsa_circ_237918,RMVar_hsa_circ_237919 113904 RMVar_ID_113904 Human_SNP_ID_863524462 m1A Human chr6 - 27230541 27230541 27230541 TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTACTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG TCGAGCCCCACTCCCGGTAAGCGTTGGTGTGTGCTTTGACGTTTGCGGTTTCTGCCGCAGAGTTG T C lnc-POM121L2-3 RNACentral:URS0000D5BC91 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:27230401..27230575 26863196 MeRIP-seq:(Medium) rs9468014 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_270797,Human_RBP_ID_659606,Human_RBP_ID_1216752,Human_RBP_ID_1669302,Human_RBP_ID_2016999,Human_RBP_ID_3001264,Human_RBP_ID_3804591,Human_RBP_ID_4877076,Human_RBP_ID_5216223,Human_RBP_ID_8269898,Human_RBP_ID_8640455,Human_RBP_ID_15771837,Human_RBP_ID_17198361,Human_RBP_ID_18861038,Human_RBP_ID_21316035,Human_RBP_ID_22830599,Human_RBP_ID_23138205,Human_RBP_ID_24153948,Human_RBP_ID_24511962,Human_RBP_ID_26534682,Human_RBP_ID_26714315,Human_RBP_ID_27094081,Human_RBP_ID_27160964,Human_RBP_ID_27344284 GWAS_ID_8227,GWAS_ID_8228,GWAS_ID_8229,GWAS_ID_8230 113905 RMVar_ID_113905 Human_SNP_ID_863527520 m1A Human chr6 + 21596272 21596269 21596273 ATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT ATTGTTGTTATTGATGTTGTTGTTGATGGC____AAAAAAAAGCGACTTCGAGTTTGCTCCCCTT CAAAA C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596221..21596370 26863196 MeRIP-seq:(Medium) rs796555280 Functional Loss DEL TCGA 31..34 33 COAD 4 - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 113906 RMVar_ID_113906 Human_SNP_ID_863536921 m1A Human chr6 - 31145046 31145046 31145046 TTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCAAGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAGC TTTAGGGGAGGCAGAGCGGCAGCAGCTGAGCAGGGTGGCCCAGCAGCTGGAGCAGGAGCTGCAGC T C CCHCR1 Ensembl:ENSG00000204536 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31144639..31145114 26863196 MeRIP-seq:(Medium) rs2073720 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,LAML,oesophagus squamous_cell_carcinoma 9 oesophagus,breast Human_RBP_ID_17710456,Human_RBP_ID_18073388,Human_RBP_ID_19017986,Human_RBP_ID_27842411 Human_Splice_Rec_751248,Human_Splice_Rec_751282,Human_Splice_Rec_751312,Human_Splice_Rec_751348,Human_Splice_Rec_751384,Human_Splice_Rec_751418,Human_Splice_Rec_751430,Human_Splice_Rec_751464 113907 RMVar_ID_113907 Human_SNP_ID_863557329 m1A Human chr6 + 71391939 71391939 71391939 CCAGCCTCATTTTCCTCTTCCTCCTCCTCTGCAGGCTCCTTTGAGCCACCCTCCTTGATGCCTCT CCAGCCTCATTTTCCTCTTCCTCCTCCTCTGCTGGCTCCTTTGAGCCACCCTCCTTGATGCCTCT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:71391675..71392041 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 113908 RMVar_ID_113908 Human_SNP_ID_863609239 m1A Human chr6 + 16143775 16143775 16143775 ATGTATATTTGACGGTCACCAAGGAATCTGGGAACAGCATCGTGCTCTTGTTTAAAATGATCAGC ATGTATATTTGACGGTCACCAAGGAATCTGGGGACAGCATCGTGCTCTTGTTTAAAATGATCAGC A G MYLIP Ensembl:ENSG00000007944 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:16143202..16143783 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 2 pancreas Human_RBP_ID_1666678,Human_RBP_ID_7568840,Human_RBP_ID_9309106,Human_RBP_ID_15718599,Human_RBP_ID_21902742 Human_Splice_Rec_740042,Human_Splice_Rec_740050 113909 RMVar_ID_113909 Human_SNP_ID_863660765 m1A Human chr6 + 116279277 116279277 116279277 GCTGCTCCTCTACCTCCATCTGCTCCTCCATTACCTCCTTCTCCGCCAGGCCTTCCTTCACCACC GCTGCTCCTCTACCTCCATCTGCTCCTCCATTCCCTCCTTCTCCGCCAGGCCTTCCTTCACCACC A C DSE Ensembl:ENSG00000111817 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:116279226..116279492 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 haematopoietic and lymphoid tissue 113910 RMVar_ID_113910 Human_SNP_ID_863707119 m1A Human chr6 - 73519373 73519373 73519373 TATGTGACTATCATTGATGCCCCAGGACACAGAGACTTTATCAAAAACATGATTACAGGGACATC TATGTGACTATCATTGATGCCCCAGGACACAGGGACTTTATCAAAAACATGATTACAGGGACATC T C EEF1A1 Ensembl:ENSG00000156508 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:73519258..73519373 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_80897,Human_RBP_ID_270877,Human_RBP_ID_667923,Human_RBP_ID_790533,Human_RBP_ID_951271,Human_RBP_ID_1328435,Human_RBP_ID_1675920,Human_RBP_ID_2026000,Human_RBP_ID_3017347,Human_RBP_ID_3814633,Human_RBP_ID_4896998,Human_RBP_ID_5217765,Human_RBP_ID_5618141,Human_RBP_ID_7627233,Human_RBP_ID_8648815,Human_RBP_ID_8903227,Human_RBP_ID_9198298,Human_RBP_ID_10296629,Human_RBP_ID_15875645,Human_RBP_ID_17307972,Human_RBP_ID_17536922,Human_RBP_ID_17711242,Human_RBP_ID_18195637,Human_RBP_ID_18539209,Human_RBP_ID_18869075,Human_RBP_ID_22106498,Human_RBP_ID_22314430,Human_RBP_ID_22406100,Human_RBP_ID_22832195,Human_RBP_ID_23069537,Human_RBP_ID_23214883,Human_RBP_ID_24171140,Human_RBP_ID_24513135,Human_RBP_ID_26049031,Human_RBP_ID_26541410,Human_RBP_ID_26717456,Human_RBP_ID_26828633,Human_RBP_ID_27100671,Human_RBP_ID_27348930,Human_RBP_ID_27525928 Human_Splice_Rec_786731,Human_Splice_Rec_786745,Human_Splice_Rec_786759,Human_Splice_Rec_786771,Human_Splice_Rec_786781,Human_Splice_Rec_786785,Human_Splice_Rec_786797,Human_Splice_Rec_786815,Human_Splice_Rec_786821 Human_miRNA_ID_2062760,Human_miRNA_ID_2900430 RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_82325,RMVar_hsa_circ_120425,RMVar_hsa_circ_239520,RMVar_hsa_circ_95017,RMVar_hsa_circ_239522,RMVar_hsa_circ_79509,RMVar_hsa_circ_239521,RMVar_hsa_circ_79498,RMVar_hsa_circ_107395,RMVar_hsa_circ_110289,RMVar_hsa_circ_239528,RMVar_hsa_circ_239530,RMVar_hsa_circ_239531,RMVar_hsa_circ_239529,RMVar_hsa_circ_116111,RMVar_hsa_circ_120353,RMVar_hsa_circ_118434,RMVar_hsa_circ_239534,RMVar_hsa_circ_239533,RMVar_hsa_circ_239537,RMVar_hsa_circ_109744,RMVar_hsa_circ_239536 113911 RMVar_ID_113911 Human_SNP_ID_863723384 m1A Human chr6 - 27893489 27893489 27893489 GTTACGGCTTTCTTGGAGCCCTTTTTGGGGGCAGGAGCAGATTTAGCCGGGTCGGGCATGGCGGA GTTACGGCTTTCTTGGAGCCCTTTTTGGGGGCCGGAGCAGATTTAGCCGGGTCGGGCATGGCGGA T G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr6:27893426..27893625;chr6:27893426..27893605 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 113912 RMVar_ID_113912 Human_SNP_ID_863743273 m1A Human chr6 + 36978527 36978527 36978527 GTGGGCTCACCTTCTTCATGCTACCCCGAGTCACAGTAGAGAGGGCGTTGGACATCAGCCGGGGA GTGGGCTCACCTTCTTCATGCTACCCCGAGTCTCAGTAGAGAGGGCGTTGGACATCAGCCGGGGA A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36978501..36978600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 113913 RMVar_ID_113913 Human_SNP_ID_863743308 m1A Human chr6 + 36978527 36978527 36978527 GTGGGCTCACCTTCTTCATGCTACCCCGAGTCACAGTAGAGAGGGCGTTGGACATCAGCCGGGGA GTGGGCTCACCTTCTTCATGCTACCCCGAGTCCCAGTAGAGAGGGCGTTGGACATCAGCCGGGGA A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:36978501..36978600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung 113914 RMVar_ID_113914 Human_SNP_ID_863785871 m1A Human chr6 + 31892872 31892869 31892873 CCCAGTGAGTGGACATCATCACTCATGCGGAAATGCTGTATTTCAGGGGGCCGCTTCTCAGGGAC CCCAGTGAGTGGACATCATCACTCATGCGG____GCTGTATTTCAGGGGGCCGCTTCTCAGGGAC GAAAT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31892827..31893028 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 PRAD 1 - 113915 RMVar_ID_113915 Human_SNP_ID_863791086 m1A Human chr6 - 26659701 26659701 26659701 CCTCTTCCCAGCCAGCTTGAAAGGGTTTGCGTAGCCGGCCTTGTGGGCCCTTGAAGCGCTCTGTT CCTCTTCCCAGCCAGCTTGAAAGGGTTTGCGTTGCCGGCCTTGTGGGCCCTTGAAGCGCTCTGTT T A ZNF322 Ensembl:ENSG00000181315 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:26659602..26659713 26863196 MeRIP-seq:(Medium) rs948247356 Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 5 uterus Human_RBP_ID_659483,Human_RBP_ID_4903741 113916 RMVar_ID_113916 Human_SNP_ID_863801095 m1A Human chr6 - 82365014 82365014 82365014 CCCAGCCCAGGAGTACCAGCGCTAGTCGCGCCAGCCGCAGACGCCCGTCCCCGGCGGCGGGGCCC CCCAGCCCAGGAGTACCAGCGCTAGTCGCGCCGGCCGCAGACGCCCGTCCCCGGCGGCGGGGCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:82364966..82365108 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113917 RMVar_ID_113917 Human_SNP_ID_863852419 m1A Human chr6 - 36596693 36596693 36596693 AAACATCTACAGTTAAAACCACAGATCCTTAGAAAGAACTCCATTAGAGAGGACAAGAGAGTTTA AAACATCTACAGTTAAAACCACAGATCCTTAGGAAGAACTCCATTAGAGAGGACAAGAGAGTTTA T C RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:36596690..36596850 26863410 MeRIP-seq:(Medium) rs60049609 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue GWAS_ID_9184 113918 RMVar_ID_113918 Human_SNP_ID_863860416 m1A Human chr6 - 79234638 79234638 79234638 CTACGTCGTGCCCTGCGCGTGAGCAGCTGCAGAGGCAGAGGCAGCATCCAGCGGCGGCGCCAGCA CTACGTCGTGCCCTGCGCGTGAGCAGCTGCAGCGGCAGAGGCAGCATCCAGCGGCGGCGCCAGCA T G HMGN3 Ensembl:ENSG00000118418 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9361504 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_4898641 Human_Splice_Rec_789545,Human_Splice_Rec_789555,Human_Splice_Rec_789565 113919 RMVar_ID_113919 Human_SNP_ID_863864610 m1A Human chr6 + 30740266 30740266 30740266 TAATCTCTCTGTGCCTTGGCCATCTCGATCTCACTCAGGTACTGAGCAGACACCTTTTCCTGCTT TAATCTCTCTGTGCCTTGGCCATCTCGATCTCGCTCAGGTACTGAGCAGACACCTTTTCCTGCTT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30740151..30740325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 113920 RMVar_ID_113920 Human_SNP_ID_863882856 m1A Human chr6 + 30583687 30583687 30583687 TGCAGACCTGTACATTGTAGCCGGCCGCCGCTACGGGCTGGTAGGACCCAATGGGTGAGAAGAGG TGCAGACCTGTACATTGTAGCCGGCCGCCGCTGCGGGCTGGTAGGACCCAATGGGTGAGAAGAGG A G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1217073,Human_RBP_ID_7591024,Human_RBP_ID_8899635,Human_RBP_ID_9400186,Human_RBP_ID_18073088,Human_RBP_ID_18450075,Human_RBP_ID_21902287 Human_Splice_Rec_748906,Human_Splice_Rec_748907,Human_Splice_Rec_748954,Human_Splice_Rec_748986,Human_Splice_Rec_748987,Human_Splice_Rec_749020,Human_Splice_Rec_749021 Human_miRNA_ID_2986567 RMVar_hsa_circ_92850,RMVar_hsa_circ_237809 113921 RMVar_ID_113921 Human_SNP_ID_863891071 m1A Human chr6 + 151351206 151351206 151351206 AAGCCGCACTGTTAACTGAGGAGGTATTGGAAAGAGAAGTAATTGCAGAAGAAGAACCCCCCACG AAGCCGCACTGTTAACTGAGGAGGTATTGGAACGAGAAGTAATTGCAGAAGAAGAACCCCCCACG A C AKAP12 Ensembl:ENSG00000131016 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:151351157..151351404 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_2011563,Human_RBP_ID_8897534 Human_miRNA_ID_3116907 RMVar_hsa_circ_242338,RMVar_hsa_circ_273069,RMVar_hsa_circ_242337 113922 RMVar_ID_113922 Human_SNP_ID_863935664 m1A Human chr6 + 31829866 31829866 31829866 GGGAGGGTCTGGGTCAGGCCCTACCATTGAGGAGGTGGATTAGGGGCCTTTGTTCTTTAGTATGT GGGAGGGTCTGGGTCAGGCCCTACCATTGAGGGGGTGGATTAGGGGCCTTTGTTCTTTAGTATGT A G HSPA1B,AL671762.1 Ensembl:ENSG00000204388,Ensembl:ENSG00000285565 Protein coding,lincRNA CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31829801..31829950;chr6:31829601..31829925;chr6:31829732..31829925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus Human_RBP_ID_13399,Human_RBP_ID_791288,Human_RBP_ID_1217271,Human_RBP_ID_1678483,Human_RBP_ID_2018754,Human_RBP_ID_3806414,Human_RBP_ID_4882284,Human_RBP_ID_5151832,Human_RBP_ID_7593004,Human_RBP_ID_8900327,Human_RBP_ID_9336069,Human_RBP_ID_15787935,Human_RBP_ID_17634026,Human_RBP_ID_18425902,Human_RBP_ID_18465513,Human_RBP_ID_18863179,Human_RBP_ID_22104900,Human_RBP_ID_22461894,Human_RBP_ID_22773418,Human_RBP_ID_24157405,Human_RBP_ID_26771730,Human_RBP_ID_27096294,Human_RBP_ID_27842600 Human_miRNA_ID_209115 113923 RMVar_ID_113923 Human_SNP_ID_863938608 m1A Human chr6 - 96892876 96892876 96892876 TACGATCACAGCTTTGGAAGTAATTAACTTGTAGGCAGTAATGGAAGTTAGAGGAGTGTGTGGGA TACGATCACAGCTTTGGAAGTAATTAACTTGTTGGCAGTAATGGAAGTTAGAGGAGTGTGTGGGA T A NDUFAF4 Ensembl:ENSG00000123545 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:96892858..96892942 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113924 RMVar_ID_113924 Human_SNP_ID_863938970 m1A Human chr6 + 34762695 34762695 34762695 ATGGATGGAAGAGCAGGCTCAGAGCCTGATTGACAAAACAAGTATGTTTCAATCTCTTGTTCTGC ATGGATGGAAGAGCAGGCTCAGAGCCTGATTGGCAAAACAAGTATGTTTCAATCTCTTGTTCTGC A G SNRPC Ensembl:ENSG00000124562 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_663084,Human_RBP_ID_9350479 Human_Splice_Rec_763619,Human_Splice_Rec_763627,Human_Splice_Rec_763635,Human_Splice_Rec_763643 RMVar_hsa_circ_47598,RMVar_hsa_circ_237968,RMVar_hsa_circ_85729,RMVar_hsa_circ_342383 113925 RMVar_ID_113925 Human_SNP_ID_863981132 m1A Human chr6 + 26217022 26217022 26217022 AAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAAACGCGTTCTTCCAGGGCCGGTCTTCAGTTTCC AAGCAAGGCGGCAAAGCTCGGGCAAAAGCTAAGACGCGTTCTTCCAGGGCCGGTCTTCAGTTTCC A G H2AC8 Ensembl:ENSG00000277075 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:26217001..26217025 26863196 MeRIP-seq:(Medium) rs1217103958 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_4876312 113926 RMVar_ID_113926 Human_SNP_ID_863982193 m1A Human chr6 + 7393224 7393224 7393224 AGAAGATGAGGAGGAGGAGGGTTATGACGATGATGATGATGACTGGGACTGGGATGAAGGAGTTG AGAAGATGAGGAGGAGGAGGGTTATGACGATGTTGATGATGACTGGGACTGGGATGAAGGAGTTG A T RIOK1 Ensembl:ENSG00000124784 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7393061..7393334 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_3017050,Human_RBP_ID_3969510,Human_RBP_ID_7626509,Human_RBP_ID_9444291,Human_RBP_ID_15874223,Human_RBP_ID_24170943,Human_RBP_ID_27828244 Human_Splice_Rec_735979,Human_Splice_Rec_735993 RMVar_hsa_circ_112397,RMVar_hsa_circ_122053,RMVar_hsa_circ_115987,RMVar_hsa_circ_63429,RMVar_hsa_circ_237057,RMVar_hsa_circ_237058,RMVar_hsa_circ_237056 113927 RMVar_ID_113927 Human_SNP_ID_863996312 m1A Human chr6 - 33200339 33200339 33200339 TGGCGGCGGCGACGGCCCTGGCTGGATCCCGCAGCGGCGGCGGCGGCGGCGGTGGCAGGCGGAGA TGGCGGCGGCGACGGCCCTGGCTGGATCCCGCGGCGGCGGCGGCGGCGGCGGTGGCAGGCGGAGA T C RXRB Ensembl:ENSG00000204231 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:33199122..33200425;chr6:33200226..33200425;chr6:33199319..33200626;chr6:33199316..33200539 26863196 MeRIP-seq:(Medium) rs895096120 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_3968923,Human_RBP_ID_19016834,Human_RBP_ID_22461215 Human_Splice_Rec_760789,Human_Splice_Rec_760807,Human_Splice_Rec_760825 113928 RMVar_ID_113928 Human_SNP_ID_864005685 m1A Human chr6 + 116571588 116571588 116571588 GATCTATGGGCAAGAGCAAGGGCCACGATGACAGATTACGGCGAGGAGCAGCGCAACGAGCTGGA GATCTATGGGCAAGAGCAAGGGCCACGATGACTGATTACGGCGAGGAGCAGCGCAACGAGCTGGA A T RWDD1 Ensembl:ENSG00000111832 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:116571484..116571625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_79347,Human_RBP_ID_169321,Human_RBP_ID_4904230,Human_RBP_ID_8628363,Human_RBP_ID_9336277,Human_RBP_ID_9401033,Human_RBP_ID_15617482,Human_RBP_ID_18852271,Human_RBP_ID_24130526,Human_RBP_ID_26354336,Human_RBP_ID_26828748,Human_RBP_ID_27087179 Human_Splice_Rec_804841,Human_Splice_Rec_804853,Human_Splice_Rec_804867,Human_Splice_Rec_804879,Human_Splice_Rec_804885 RMVar_hsa_circ_241097,RMVar_hsa_circ_111308 113929 RMVar_ID_113929 Human_SNP_ID_864014776 m1A Human chr6 - 31356259 31356259 31356259 GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGCGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG T G HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31356151..31356450 32194978 MeRIP-seq:(Medium) rs151341293 Functional Loss SNV COSMIC 33..33 33 breast metaplastic_carcinoma 2 breast Human_RBP_ID_17663950,Human_RBP_ID_18472044,Human_RBP_ID_22461067,Human_RBP_ID_22773395,Human_RBP_ID_24156743 Human_Splice_Rec_751777,Human_Splice_Rec_751791,Human_Splice_Rec_751805,Human_Splice_Rec_751809 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 113930 RMVar_ID_113930 Human_SNP_ID_864014777 m1A Human chr6 - 31356259 31356259 31356259 GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGAGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG GATCACCCAGCGCAAGTGGGAGGCGGCCCGTGTGGCGGAGCAGCGGAGAGCCTACCTGGAGGGCG T A HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31356151..31356450 32194978 MeRIP-seq:(Medium) rs151341293 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 48 head and neck,large intestine Human_RBP_ID_17663950,Human_RBP_ID_18472044,Human_RBP_ID_22461067,Human_RBP_ID_22773395,Human_RBP_ID_24156743 Human_Splice_Rec_751777,Human_Splice_Rec_751791,Human_Splice_Rec_751805,Human_Splice_Rec_751809 RMVar_hsa_circ_82534,RMVar_hsa_circ_237823 113931 RMVar_ID_113931 Human_SNP_ID_864024161 m1A Human chr6 + 75085225 75085225 75085225 CTGCCCGGGTCCGTGGGGCAGGGCGCGCCGCCAGCGCCGGTGGGGCTCAGGAGGCTCCTCTGCAG CTGCCCGGGTCCGTGGGGCAGGGCGCGCCGCCTGCGCCGGTGGGGCTCAGGAGGCTCCTCTGCAG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:75085176..75085250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver 113932 RMVar_ID_113932 Human_SNP_ID_864081000 m1A Human chr6 + 31634873 31634873 31634873 GACTCAAGGGGGCAGCAGAGGGACCCCCCAAGAGGCCTGGAGGCTCCTCACCCCTGAATGCTGTT GACTCAAGGGGGCAGCAGAGGGACCCCCCAAGCGGCCTGGAGGCTCCTCACCCCTGAATGCTGTT A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31634826..31634917 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_661505,Human_RBP_ID_1395114,Human_RBP_ID_7592609,Human_RBP_ID_8642182,Human_RBP_ID_8900163,Human_RBP_ID_9354636,Human_RBP_ID_18862967 113933 RMVar_ID_113933 Human_SNP_ID_864103793 m1A Human chr6 - 26158190 26158190 26158190 GCCTTCTTGGAGCCCTTCTTTGGGGCAGGAGCAGACTTGGTAGGTTCAGGCATCGTAGCGTTAAT GCCTTCTTGGAGCCCTTCTTTGGGGCAGGAGCTGACTTGGTAGGTTCAGGCATCGTAGCGTTAAT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:26158126..26158283;chr6:26158126..26158275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_93634,RMVar_hsa_circ_237741 113934 RMVar_ID_113934 Human_SNP_ID_864107692 m1A Human chr6 + 75119092 75119092 75119092 AAAGCCGCCTTCTTGACCTCATCCTGGGACCGACCGTCCGTGACCACAACCAACACCTTAGGGAC AAAGCCGCCTTCTTGACCTCATCCTGGGACCGGCCGTCCGTGACCACAACCAACACCTTAGGGAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:75119026..75119208 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 10 large intestine 113935 RMVar_ID_113935 Human_SNP_ID_864133689 m1A Human chr6 + 21596271 21596269 21596272 GATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCT GATTGTTGTTATTGATGTTGTTGTTGATGGC___AAAAAAAAAGCGACTTCGAGTTTGCTCCCCT CAAA C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:21596220..21596315 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 COAD,READ,DLBC 12 - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 113936 RMVar_ID_113936 Human_SNP_ID_864133689 m1A Human chr6 + 21596272 21596269 21596272 ATTGTTGTTATTGATGTTGTTGTTGATGGCAAAAAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT ATTGTTGTTATTGATGTTGTTGTTGATGGC___AAAAAAAAAGCGACTTCGAGTTTGCTCCCCTT CAAA C SOX4 Ensembl:ENSG00000124766 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:21596221..21596370 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 COAD,READ,DLBC 12 - Human_RBP_ID_658555,Human_RBP_ID_1111312,Human_RBP_ID_1668458,Human_RBP_ID_2016356,Human_RBP_ID_18860171,Human_RBP_ID_27343713 Human_miRNA_ID_186530 113937 RMVar_ID_113937 Human_SNP_ID_864165252 m1A Human chr6 + 131808114 131808114 131808114 GCGGGCGCGCTCCCCGGGAGGGCCCGGCGGGGAACGGCCGCGATCGGGGCCGCAGCCACGCTGCC GCGGGCGCGCTCCCCGGGAGGGCCCGGCGGGGGACGGCCGCGATCGGGGCCGCAGCCACGCTGCC A G ENPP1 Ensembl:ENSG00000197594 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:131808066..131808203 26863196 MeRIP-seq:(Medium) rs985103461 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3821805,Human_RBP_ID_4903511,Human_RBP_ID_5533214,Human_RBP_ID_8730320,Human_RBP_ID_9354662 113938 RMVar_ID_113938 Human_SNP_ID_864219168 m1A Human chr6 - 89411935 89411935 89411935 GCCGCAGGACGAGGACGACGCGGAGGAGGAGGAGGAGGAGGATGAGCTGGTGGGGCTAGCGGACT GCCGCAGGACGAGGACGACGCGGAGGAGGAGGGGGAGGAGGATGAGCTGGTGGGGCTAGCGGACT T C RRAGD Ensembl:ENSG00000025039 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:89411885..89411988 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_4901062 Human_Splice_Rec_794529,Human_Splice_Rec_794541 113939 RMVar_ID_113939 Human_SNP_ID_864227081 m1A Human chr6 - 165794690 165794689 165794690 TAGTGGTTTTTTTGTGTGGGTGAAATGAGAAAATATTCCTGTCAGTGTGTGAGTTATTGAGTGTG TAGTGGTTTTTTTGTGTGGGTGAAATGAGAAA_TATTCCTGTCAGTGTGTGAGTTATTGAGTGTG AT A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165794155..165794725 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 CHOL 1 - 113940 RMVar_ID_113940 Human_SNP_ID_864244137 m1A Human chr6 - 3006561 3006561 3006561 AAAAAAGTCTTACTCCACAATAGTGAATCATTACCTGCCATAGCGTAAGAAGGTGGATTCCTTCT AAAAAAGTCTTACTCCACAATAGTGAATCATTCCCTGCCATAGCGTAAGAAGGTGGATTCCTTCT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:3006526..3006575 26863196 MeRIP-seq:(Medium) rs762221263 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113941 RMVar_ID_113941 Human_SNP_ID_864246576 m1A Human chr6 - 2766141 2766129 2766141 TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCCATCGCCGTCGCCCACGGCCTCCTCCTCCTCCTG TCCTCGCCGTCCGCGTCCGCGTCCCCGTCGCC____________CACGGCCTCCTCCTCCTCCTG GGGCGACGGCGAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:2765389..2766441;chr6:2765351..2768750;chr6:2765376..2766450;chr6:2765351..2766450 26863196 MeRIP-seq:(Medium) rs535821800 Functional Loss DEL ICGC 33..44 33 PBCA 1 - 113942 RMVar_ID_113942 Human_SNP_ID_864253016 m1A Human chr6 + 34950559 34950558 34950560 CCAGGAAGACGTTTTTCAAGACTATTACAATAAGAGAGAGAGAGATCCGGCTTAACTCCAAATAT CCAGGAAGACGTTTTTCAAGACTATTACAATA__AGAGAGAGAGATCCGGCTTAACTCCAAATAT AAG A ANKS1A Ensembl:ENSG00000064999 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:34950556..34950641 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 LICA 1 - Human_RBP_ID_15802152 113943 RMVar_ID_113943 Human_SNP_ID_864258455 m1A Human chr6 + 31624312 31624312 31624312 CAGCCGCCGGAATCGCAGCCACTGCCGGCTTCACAGACGCCTGCCTCCAACCAGCCGAAACGACC CAGCCGCCGGAATCGCAGCCACTGCCGGCTTCCCAGACGCCTGCCTCCAACCAGCCGAAACGACC A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31624233..31624525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_252596,Human_RBP_ID_661460,Human_RBP_ID_1046814,Human_RBP_ID_8642086,Human_RBP_ID_8900007,Human_RBP_ID_17306484,Human_RBP_ID_18073578,Human_RBP_ID_18862861,Human_RBP_ID_23060240 Human_Splice_Rec_752452,Human_Splice_Rec_752453,Human_Splice_Rec_752512,Human_Splice_Rec_752513,Human_Splice_Rec_752568,Human_Splice_Rec_752569 113944 RMVar_ID_113944 Human_SNP_ID_864273884 m1A Human chr6 - 31829660 31829660 31829660 AGCCACGAGATGACCTCTTGACACTTGTCCAGAACCTTCTTCTTGTCCGCCTCGCTGATCTTGCC AGCCACGAGATGACCTCTTGACACTTGTCCAGCACCTTCTTCTTGTCCGCCTCGCTGATCTTGCC T G RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31829601..31829725 32194978 MeRIP-seq:(Medium) rs35682610 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,thyroid neoplasm 2 head and neck 113945 RMVar_ID_113945 Human_SNP_ID_864283772 m1A Human chr6 - 52995884 52995884 52995884 TTGGATGTGTCTGGAGTCTTGGAAGCTTGACTACCCTACGTTCTCCTACAAATGGACCTTGAGAG TTGGATGTGTCTGGAGTCTTGGAAGCTTGACTCCCCTACGTTCTCCTACAAATGGACCTTGAGAG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:52995826..52995925 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 113946 RMVar_ID_113946 Human_SNP_ID_864289086 m1A Human chr6 - 29942585 29942585 29942585 TCTGGGTCAGGGCCAGGGCCCCCGAGAGTAGCAGGAGGAGGGTTCGGGGCGCCATGACGGCCATC TCTGGGTCAGGGCCAGGGCCCCCGAGAGTAGCCGGAGGAGGGTTCGGGGCGCCATGACGGCCATC T G AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:29942526..29942650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue Human_RBP_ID_1678755,Human_RBP_ID_17538248 113947 RMVar_ID_113947 Human_SNP_ID_864306747 m1A Human chr6 + 34883045 34883045 34883045 GCAGGATTAAGTAATGATGAGTCTTCCCTTTCAACTGTTGTTAAATCTGAGACATCCTGACTCTC GCAGGATTAAGTAATGATGAGTCTTCCCTTTCGACTGTTGTTAAATCTGAGACATCCTGACTCTC A G UHRF1BP1 Ensembl:ENSG00000065060 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:34883001..34883050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung 113948 RMVar_ID_113948 Human_SNP_ID_864308918 m1A Human chr6 - 15374076 15374076 15374076 ACATAAGAAAAGAGAGGAGTTACTGAATAGAAAGCAAGGCAATATTCAGAGTCAAAATAAACTTT ACATAAGAAAAGAGAGGAGTTACTGAATAGAATGCAAGGCAATATTCAGAGTCAAAATAAACTTT T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:15374067..15374186 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113949 RMVar_ID_113949 Human_SNP_ID_864314308 m1A Human chr6 - 27838625 27838624 27838625 GGGAGTAACTGCCGGAAAATTGGAGGAAAAAAACAGGAAGACGGTAGCTCTGTCAACCTACCGCT GGGAGTAACTGCCGGAAAATTGGAGGAAAAAA_CAGGAAGACGGTAGCTCTGTCAACCTACCGCT GT G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:27838576..27838745 26863196 MeRIP-seq:(Medium) rs770490807 Functional Loss DEL TCGA,ICGC 33..33 33 STAD,UCEC,ESCA 4 - 113950 RMVar_ID_113950 Human_SNP_ID_864342939 m1A Human chr6 - 30580007 30580007 30580007 CCCCAATACCTCCTCCTGCTAGTTACTCTCTCACCTTAGCCTTCCCTTTTGACTTCTCTTCCTTT CCCCAATACCTCCTCCTGCTAGTTACTCTCTCGCCTTAGCCTTCCCTTTTGACTTCTCTTCCTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30579926..30580025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 113951 RMVar_ID_113951 Human_SNP_ID_864348138 m1A Human chr6 + 29944376 29944376 29944376 ACACCTGCCATGTGCAGCATGAGGGTCTGCCCAAGCCCCTCACCCTGAGATGGGGTAAGGAGGGA ACACCTGCCATGTGCAGCATGAGGGTCTGCCCGAGCCCCTCACCCTGAGATGGGGTAAGGAGGGA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29944326..29944375 26863196 MeRIP-seq:(Medium) rs1136835 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,pancreas ductal_carcinoma,oesophagus squamous_cell_carcinoma,lung adenocarcinoma,ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 47 lung,oesophagus,pancreas,head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_18085724,Human_RBP_ID_22773335 Human_Splice_Rec_747845,Human_Splice_Rec_747859,Human_Splice_Rec_747873,Human_Splice_Rec_747887,Human_Splice_Rec_747899,Human_Splice_Rec_747905,Human_Splice_Rec_747919,Human_Splice_Rec_747927,Human_Splice_Rec_747937 Human_miRNA_ID_191307,Human_miRNA_ID_829992,Human_miRNA_ID_1235579,Human_miRNA_ID_1561887 113952 RMVar_ID_113952 Human_SNP_ID_864362102 m1A Human chr6 - 31647779 31647779 31647779 CAACCGCAGCACAGTCAGCCGCCCCCGCAGCCACCGGCTGTGACCCCGGAGCCAGTAGCCTTGAG CAACCGCAGCACAGTCAGCCGCCCCCGCAGCCGCCGGCTGTGACCCCGGAGCCAGTAGCCTTGAG T C BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31647539..31647856 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_252590,Human_RBP_ID_18195451,Human_RBP_ID_22514044,Human_RBP_ID_26828211 Human_Splice_Rec_752654,Human_Splice_Rec_752702,Human_Splice_Rec_752796,Human_Splice_Rec_752842,Human_Splice_Rec_752898,Human_Splice_Rec_752954,Human_Splice_Rec_752976,Human_Splice_Rec_752988,Human_Splice_Rec_752998,Human_Splice_Rec_753010,Human_Splice_Rec_753020,Human_Splice_Rec_753032,Human_Splice_Rec_753044,Human_Splice_Rec_753054,Human_Splice_Rec_753064,Human_Splice_Rec_753074 113953 RMVar_ID_113953 Human_SNP_ID_864366105 m1A Human chr6 - 122437175 122437175 122437175 ACTATACACACACACACACACACACACACACAAAAATATATGTGTACAAAATCAAATACATTGTT ACTATACACACACACACACACACACACACACACAAATATATGTGTACAAAATCAAATACATTGTT T G Z99129.4 Ensembl:ENSG00000279453 Other exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs546653 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113954 RMVar_ID_113954 Human_SNP_ID_864389966 m1A Human chr6 - 24701575 24701575 24701575 CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATTAATTTTCCTGTGGCCTTGTTGGTCAGATCCACA CCAGGTGTTTTGTGTGTCTTCCTTGTGCTATTCATTTTCCTGTGGCCTTGTTGGTCAGATCCACA T G AL031775.1 Ensembl:ENSG00000272345 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:24701525..24701605 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_3000481,Human_RBP_ID_3803848 113955 RMVar_ID_113955 Human_SNP_ID_864404735 m1A Human chr6 + 28729371 28729371 28729371 GCGTGCTTCGCATGTACGAGGCCCCGGGTTCGACCCCCGGCTCCTCCAGTTGTCCATTTTCTTCA GCGTGCTTCGCATGTACGAGGCCCCGGGTTCGTCCCCCGGCTCCTCCAGTTGTCCATTTTCTTCA A T - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq;HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:28729323..28729423;chr6:28729328..28729463;chr6:28729328..28729429;chr6:28729317..28729487 29072297,31548705,26863196 m1A-MAP&m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 113956 RMVar_ID_113956 Human_SNP_ID_864420180 m1A Human chr6 - 18258402 18258401 18258403 TAATTAAGAAATACTAAATTAATTTCTAGAAAAGAGTCTCATCGTGGAAGGCAAGAGGGAAAAGA TAATTAAGAAATACTAAATTAATTTCTAGAA__GAGTCTCATCGTGGAAGGCAAGAGGGAAAAGA CTT C DEK Ensembl:ENSG00000124795 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:18258351..18258425 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 STAD 1 - Human_RBP_ID_658313,Human_RBP_ID_792139,Human_RBP_ID_2015727,Human_RBP_ID_2997433,Human_RBP_ID_7579424,Human_RBP_ID_9400004,Human_RBP_ID_15754094,Human_RBP_ID_17663222,Human_RBP_ID_23116418,Human_RBP_ID_24150816,Human_RBP_ID_24548544,Human_RBP_ID_26353441,Human_RBP_ID_27827350 Human_Splice_Rec_741184,Human_Splice_Rec_741185,Human_Splice_Rec_741210,Human_Splice_Rec_741211,Human_Splice_Rec_741224,Human_Splice_Rec_741225,Human_Splice_Rec_741244,Human_Splice_Rec_741245,Human_Splice_Rec_741266,Human_Splice_Rec_741267,Human_Splice_Rec_741284,Human_Splice_Rec_741285,Human_Splice_Rec_741322,Human_Splice_Rec_741323,Human_Splice_Rec_741346,Human_Splice_Rec_741347,Human_Splice_Rec_741356,Human_Splice_Rec_741357 RMVar_hsa_circ_62800,RMVar_hsa_circ_358479,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,RMVar_hsa_circ_65487,RMVar_hsa_circ_317221,RMVar_hsa_circ_283292,RMVar_hsa_circ_237485,RMVar_hsa_circ_64068,RMVar_hsa_circ_27303,RMVar_hsa_circ_237486,RMVar_hsa_circ_237487,RMVar_hsa_circ_68404,RMVar_hsa_circ_272868,RMVar_hsa_circ_237488,RMVar_hsa_circ_296652,RMVar_hsa_circ_361870 113957 RMVar_ID_113957 Human_SNP_ID_864466688 m1A Human chr6 + 19837738 19837738 19837738 CCTCGCTCGCCCCAGCGGGTTCGCTCGCGTAGAGCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC CCTCGCTCGCCCCAGCGGGTTCGCTCGCGTAGGGCGCAGGGCGCGCGCGATGAAGGCGGTGAGCC A G ID4 Ensembl:ENSG00000172201 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:19837645..19838025 26863410 MeRIP-seq:(Medium) rs12662234 Functional Loss SNV ICGC 33..33 33 LICA 1 - 113958 RMVar_ID_113958 Human_SNP_ID_864492157 m1A Human chr6 + 31635741 31635741 31635741 CTGAGGTTTTCTATGGCAGTGCTGGGCCTTCCAGTTCTCAGGTAGGCCCCGCTTCCCATTGCATG CTGAGGTTTTCTATGGCAGTGCTGGGCCTTCCCGTTCTCAGGTAGGCCCCGCTTCCCATTGCATG A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31635576..31635781 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_661513,Human_RBP_ID_1046850,Human_RBP_ID_3968724,Human_RBP_ID_4903190,Human_RBP_ID_8905246,Human_RBP_ID_9262962,Human_RBP_ID_17310189,Human_RBP_ID_18073653,Human_RBP_ID_18195424,Human_RBP_ID_19128863 Human_Splice_Rec_752493,Human_Splice_Rec_752553 113959 RMVar_ID_113959 Human_SNP_ID_864507794 m1A Human chr6 - 158818160 158818160 158818160 CTCTAAGGGTTCTGCTCTGACTCCAGGTTGGGACAGCGTCTTCGCTGCTGCTGGATAGTCGTGTT CTCTAAGGGTTCTGCTCTGACTCCAGGTTGGGGCAGCGTCTTCGCTGCTGCTGGATAGTCGTGTT T C EZR Ensembl:ENSG00000092820 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:158789466..158818223 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_79098,Human_RBP_ID_4904342,Human_RBP_ID_19132301 Human_Splice_Rec_828619,Human_Splice_Rec_828662,Human_Splice_Rec_828663,Human_Splice_Rec_828686,Human_Splice_Rec_828687 Human_miRNA_ID_2099288,Human_miRNA_ID_2099289,Human_miRNA_ID_2099290,Human_miRNA_ID_2105240,Human_miRNA_ID_2105241,Human_miRNA_ID_2105242,Human_miRNA_ID_2111190,Human_miRNA_ID_2111191,Human_miRNA_ID_2111192,Human_miRNA_ID_2163736,Human_miRNA_ID_2163737,Human_miRNA_ID_2163738,Human_miRNA_ID_2594957,Human_miRNA_ID_2594958,Human_miRNA_ID_2594959,Human_miRNA_ID_2737901,Human_miRNA_ID_2737902,Human_miRNA_ID_2737903,Human_miRNA_ID_2756309,Human_miRNA_ID_2756310,Human_miRNA_ID_2756311 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_125699,RMVar_hsa_circ_242771,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_332275,RMVar_hsa_circ_97977,RMVar_hsa_circ_19359,RMVar_hsa_circ_110280,RMVar_hsa_circ_242789,RMVar_hsa_circ_242790 113960 RMVar_ID_113960 Human_SNP_ID_864508333 m1A Human chr6 + 30578191 30578191 30578191 TCTTAAGAAGCTCTCAGTGCCAACCAGTGATGAGGAGGATGAAGGTAAATGACCTGAGGGGGAAT TCTTAAGAAGCTCTCAGTGCCAACCAGTGATGCGGAGGATGAAGGTAAATGACCTGAGGGGGAAT A C ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30578142..30578387 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_2017993,Human_RBP_ID_7591003,Human_RBP_ID_9350419,Human_RBP_ID_19130327,Human_RBP_ID_24178819,Human_RBP_ID_24548672,Human_RBP_ID_24554604,Human_RBP_ID_26353142,Human_RBP_ID_27827424 Human_Splice_Rec_748895,Human_Splice_Rec_748941,Human_Splice_Rec_748959,Human_Splice_Rec_748973,Human_Splice_Rec_749015 113961 RMVar_ID_113961 Human_SNP_ID_864514047 m1A Human chr6 + 32117598 32117598 32117598 CCCCAGCAATGAATCCCACACCTCAGGGACTCAGTGCGGTTGAAGTGCCGGCAATCAGAGGAGAG CCCCAGCAATGAATCCCACACCTCAGGGACTCGGTGCGGTTGAAGTGCCGGCAATCAGAGGAGAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:32117333..32117615 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 113962 RMVar_ID_113962 Human_SNP_ID_864531814 m1A Human chr6 + 30198856 30198856 30198856 GGGTCACCTCTCCCGGCTGCCTGCCCTTGTCCACCTTCAGCCGCTCAATGTTCTCCACCAGGCTG GGGTCACCTCTCCCGGCTGCCTGCCCTTGTCCGCCTTCAGCCGCTCAATGTTCTCCACCAGGCTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30198666..30199017 26863196 MeRIP-seq:(Medium) rs752486472 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 113963 RMVar_ID_113963 Human_SNP_ID_864555714 m1A Human chr6 + 159762086 159762086 159762086 GCAGCGCAGGGCAGACGGCGGCAGGAGAAGCAAGATGAATGCAGGCTCAGATCCTGTGGTCATCG GCAGCGCAGGGCAGACGGCGGCAGGAGAAGCACGATGAATGCAGGCTCAGATCCTGTGGTCATCG A C ACAT2 Ensembl:ENSG00000120437 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:159761876..159762161 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_4903581,Human_RBP_ID_5327585,Human_RBP_ID_8635811,Human_RBP_ID_9309448 Human_Splice_Rec_829383 113964 RMVar_ID_113964 Human_SNP_ID_864562864 m1A Human chr6 + 13616468 13616468 13616468 TAATTTTAAACGTTTTCATTCCAAAAGAAAAGAAAACTCCTTCCAGACACTATTTTGGAGAAGTT TAATTTTAAACGTTTTCATTCCAAAAGAAAAGGAAACTCCTTCCAGACACTATTTTGGAGAAGTT A G NOL7 Ensembl:ENSG00000225921 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:13616451..13616500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_214602,Human_RBP_ID_948042,Human_RBP_ID_9401620,Human_RBP_ID_22683696 Human_Splice_Rec_739582,Human_Splice_Rec_739583,Human_Splice_Rec_739596,Human_Splice_Rec_739597,Human_Splice_Rec_739602,Human_Splice_Rec_739603 RMVar_hsa_circ_55040 113965 RMVar_ID_113965 Human_SNP_ID_864582161 m1A Human chr6 - 41597857 41597857 41597857 CGGGGGCACCCACGTCATCGTGGCTGAGGGGCAGCAGGCTGCTGGCGGAGCCAGGGTTCAGCATG CGGGGGCACCCACGTCATCGTGGCTGAGGGGCTGCAGGCTGCTGGCGGAGCCAGGGTTCAGCATG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:41597176..41598897 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach 113966 RMVar_ID_113966 Human_SNP_ID_864596387 m1A Human chr6 + 42888291 42888291 42888291 ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTT ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTGCATGCATGTACCACCACACCCAGCTAATTCTT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1318315394 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4890182 113967 RMVar_ID_113967 Human_SNP_ID_864604118 m1A Human chr6 - 73765282 73765282 73765282 TCTCTTCCATCCTCTCCACTCCCACAGCTACCACCACAAGGCTGCCCATCCCCTCACTCCTGGGC TCTCTTCCATCCTCTCCACTCCCACAGCTACCGCCACAAGGCTGCCCATCCCCTCACTCCTGGGC T C RF00017-4489,lnc-BBS5-6 RNACentral:URS00009982F9,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:73765180..73765301 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113968 RMVar_ID_113968 Human_SNP_ID_864606286 m1A Human chr6 + 31791970 31791970 31791970 GGGCTGTAGGAGTCGGGCATGGGGCCACTGACATCTGGGGGAGAGGAAGGGAGGGCTCAGTGCCG GGGCTGTAGGAGTCGGGCATGGGGCCACTGACTTCTGGGGGAGAGGAAGGGAGGGCTCAGTGCCG A T RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31791851..31791975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 113969 RMVar_ID_113969 Human_SNP_ID_864618546 m1A Human chr6 + 28941142 28941142 28941142 GGATTCTGGTCTCCAATGGAGGCGTGGGTTCGAATCCCACTTCTGACACAACTATCTTATTCTCC GGATTCTGGTCTCCAATGGAGGCGTGGGTTCGCATCCCACTTCTGACACAACTATCTTATTCTCC A C RF00017-4692 RNACentral:URS000090D53C SRP RNA intron GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 113970 RMVar_ID_113970 Human_SNP_ID_864669136 m1A Human chr6 + 99412707 99412707 99412707 TTGCTGTCCTGAAGCTTCTCTTTGGGCAATCCAAGCTTGGGCCAATGCAGCCCAATCAATCTGGC TTGCTGTCCTGAAGCTTCTCTTTGGGCAATCCGAGCTTGGGCCAATGCAGCCCAATCAATCTGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:99412568..99414700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 113971 RMVar_ID_113971 Human_SNP_ID_864675318 m1A Human chr6 + 1611810 1611810 1611810 AGTCACGGCGGCGGCGGCGGCGGCGGCGGGGGAGGCCAGGAGGCCGGCCACCACCCTGCGGCCCA AGTCACGGCGGCGGCGGCGGCGGCGGCGGGGGGGGCCAGGAGGCCGGCCACCACCCTGCGGCCCA A G FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:1611763..1611950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_251951 113972 RMVar_ID_113972 Human_SNP_ID_864677981 m1A Human chr6 - 169241902 169241902 169241902 ACACAGAGACGCTGCGCCTGGGTCCGCATGTCACCACCGAGTACGTGGGCCCCAGCTCGGAGAGG ACACAGAGACGCTGCGCCTGGGTCCGCATGTCTCCACCGAGTACGTGGGCCCCAGCTCGGAGAGG T A THBS2 Ensembl:ENSG00000186340 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:169241851..169241950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_Splice_Rec_834596,Human_Splice_Rec_834638,Human_Splice_Rec_834680 RMVar_hsa_circ_89719,RMVar_hsa_circ_243063,RMVar_hsa_circ_83223,RMVar_hsa_circ_243073,RMVar_hsa_circ_116933,RMVar_hsa_circ_45599,RMVar_hsa_circ_16577,RMVar_hsa_circ_97109,RMVar_hsa_circ_243075,RMVar_hsa_circ_243077,RMVar_hsa_circ_17223,RMVar_hsa_circ_323521 113973 RMVar_ID_113973 Human_SNP_ID_864678821 m1A Human chr6 + 15627467 15627467 15627467 TCCCAGTGCGCAGAAAGCATGACCACCTCGCTATCCACCAGCTGCAGCACACAAGAAGGGGGGTA TCCCAGTGCGCAGAAAGCATGACCACCTCGCTGTCCACCAGCTGCAGCACACAAGAAGGGGGGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:15627417..15627523 26863196 MeRIP-seq:(Medium) rs1238265151 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver 113974 RMVar_ID_113974 Human_SNP_ID_864717499 m1A Human chr6 - 26285345 26285345 26285345 CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTATGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC CGGCGGTGTCAAGCGAATTTCTGGCCTTATCTGTGAGGAGACTCGTGGTGTTCTGAAGGTGTTCC T C H4C8 Ensembl:ENSG00000158406 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:26285294..26285550 26863196 MeRIP-seq:(Medium) rs751532587 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA,ESCA 3 - Human_RBP_ID_81823,Human_RBP_ID_659146,Human_RBP_ID_1046113,Human_RBP_ID_1216636,Human_RBP_ID_1326475,Human_RBP_ID_1668995,Human_RBP_ID_2016774,Human_RBP_ID_3804296,Human_RBP_ID_4876438,Human_RBP_ID_5219128,Human_RBP_ID_5428224,Human_RBP_ID_7586022,Human_RBP_ID_8640146,Human_RBP_ID_8899189,Human_RBP_ID_9336005,Human_RBP_ID_15770525,Human_RBP_ID_17306023,Human_RBP_ID_17419225,Human_RBP_ID_17535179,Human_RBP_ID_18071499,Human_RBP_ID_18369501,Human_RBP_ID_18449944,Human_RBP_ID_18860708,Human_RBP_ID_22773296,Human_RBP_ID_23137943,Human_RBP_ID_24153438,Human_RBP_ID_26828017,Human_RBP_ID_27093755,Human_RBP_ID_27344070,Human_RBP_ID_27754056 113975 RMVar_ID_113975 Human_SNP_ID_864737597 m1A Human chr6 - 1898101 1898101 1898101 GGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGATAGGTGTCCAGGATGGCAAGGGAGGCCAGGGT GGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGGTAGGTGTCCAGGATGGCAAGGGAGGCCAGGGT T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:1897899..1898234;chr6:1897952..1898133 26863196 MeRIP-seq:(Medium) rs9501781 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_18956956 RMVar_hsa_circ_74524 113976 RMVar_ID_113976 Human_SNP_ID_864738223 m1A Human chr6 - 26597091 26597091 26597091 AATACCTGGCACTACCCGTTTCTTGCTGCCACAGGCCGCTTCTTCGGATTCCTCCTGCTCCTCCT AATACCTGGCACTACCCGTTTCTTGCTGCCACGGGCCGCTTCTTCGGATTCCTCCTGCTCCTCCT T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:26597006..26597095 26863410 MeRIP-seq:(Medium) rs1554144548 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,colon adenocarcinoma,large_intestine adenocarcinoma 5 stomach,large intestine 113977 RMVar_ID_113977 Human_SNP_ID_864759528 m1A Human chr6 - 165987927 165987927 165987927 CTCATGTTCTAAAGAGAGAGGTCTGAGTCCGAAGTTGCTGCTGCTGGGAGCTTGAGCTGAGATGG CTCATGTTCTAAAGAGAGAGGTCTGAGTCCGAGGTTGCTGCTGCTGGGAGCTTGAGCTGAGATGG T C PDE10A Ensembl:ENSG00000112541 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165987877..165988050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2993974,Human_RBP_ID_4872967,Human_RBP_ID_5622092 Human_miRNA_ID_2099306,Human_miRNA_ID_2105260,Human_miRNA_ID_2111207,Human_miRNA_ID_2163753,Human_miRNA_ID_2594977,Human_miRNA_ID_2737920,Human_miRNA_ID_3038518,Human_miRNA_ID_3155673,Human_miRNA_ID_3156023,Human_miRNA_ID_3156370,Human_miRNA_ID_3159428,Human_miRNA_ID_3184877,Human_miRNA_ID_3193253,Human_miRNA_ID_3211334 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 113978 RMVar_ID_113978 Human_SNP_ID_864759530 m1A Human chr6 - 165987927 165987927 165987927 CTCATGTTCTAAAGAGAGAGGTCTGAGTCCGAAGTTGCTGCTGCTGGGAGCTTGAGCTGAGATGG CTCATGTTCTAAAGAGAGAGGTCTGAGTCCGACGTTGCTGCTGCTGGGAGCTTGAGCTGAGATGG T G PDE10A Ensembl:ENSG00000112541 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:165987877..165988050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_2993974,Human_RBP_ID_4872967,Human_RBP_ID_5622092 Human_miRNA_ID_2099306,Human_miRNA_ID_2105260,Human_miRNA_ID_2111207,Human_miRNA_ID_2163753,Human_miRNA_ID_2594977,Human_miRNA_ID_2737920,Human_miRNA_ID_3038518,Human_miRNA_ID_3155673,Human_miRNA_ID_3156023,Human_miRNA_ID_3156370,Human_miRNA_ID_3159428,Human_miRNA_ID_3184877,Human_miRNA_ID_3193253,Human_miRNA_ID_3211334 RMVar_hsa_circ_127123,RMVar_hsa_circ_242953 113979 RMVar_ID_113979 Human_SNP_ID_864776694 m1A Human chr6 - 43019123 43019123 43019123 AATGTGTAAGTCAGAATGATCTATAAGGTCAAATTCATCTCCCAGGCCTTCCTCAGGAGATGGAC AATGTGTAAGTCAGAATGATCTATAAGGTCAACTTCATCTCCCAGGCCTTCCTCAGGAGATGGAC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43019081..43019172 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 113980 RMVar_ID_113980 Human_SNP_ID_864777311 m1A Human chr6 + 26156451 26156449 26156452 CTGCTCCGGCCCCTGCCGAGAAGACTCCCGTGAAGAAGAAGGCCCGCAAGTCTGCAGGTGCGGCC CTGCTCCGGCCCCTGCCGAGAAGACTCCCGT___GAAGAAGGCCCGCAAGTCTGCAGGTGCGGCC TGAA T H1-4 Ensembl:ENSG00000168298 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:26156351..26156492 26863410 MeRIP-seq:(Medium) rs545095988 Functional Loss DEL TCGA,ICGC 32..34 33 COAD,HNSC,BLCA,ESCA,CHOL 9 - Human_RBP_ID_659039,Human_RBP_ID_1046020,Human_RBP_ID_1668872,Human_RBP_ID_2016703,Human_RBP_ID_3804201,Human_RBP_ID_4876134,Human_RBP_ID_7585688,Human_RBP_ID_8640037,Human_RBP_ID_9335992,Human_RBP_ID_9400073,Human_RBP_ID_18860597,Human_RBP_ID_22462435,Human_RBP_ID_22830371,Human_RBP_ID_24548546,Human_RBP_ID_26353118,Human_RBP_ID_26714211,Human_RBP_ID_27093666,Human_RBP_ID_27343977 113981 RMVar_ID_113981 Human_SNP_ID_864780391 m1A Human chr6 - 85593789 85593769 85593790 GTGCGCCGCCAAGTCGGTGGGGCGGGGACGCGAGGTGTGGATGGGGGGTCGCCTTGACCTCTGCC GTGCGCCGCCAAGTCGGTGGGGCGGGGACGC_____________________CTTGACCTCTGCC GGCGACCCCCCATCCACACCTC G SNX14,AL589666.1 Ensembl:ENSG00000135317,Ensembl:ENSG00000271793 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:85593740..85594156 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..52 33 LUAD 1 - Human_RBP_ID_790307,Human_RBP_ID_842033,Human_RBP_ID_4899880,Human_RBP_ID_8905431,Human_RBP_ID_22462152 RMVar_hsa_circ_83693,RMVar_hsa_circ_240027 113982 RMVar_ID_113982 Human_SNP_ID_864794499 m1A Human chr6 - 43340351 43340350 43340351 TGAGAAACCAAAGGAGGAGAAGAAAGAAAAAAAGGCAAAGGCTGTGAAAGAAGTAAAGGAGGATG TGAGAAACCAAAGGAGGAGAAGAAAGAAAAAA_GGCAAAGGCTGTGAAAGAAGTAAAGGAGGATG CT C ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43340300..43340421 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_40769,RMVar_hsa_circ_66844,RMVar_hsa_circ_107122,RMVar_hsa_circ_51086,RMVar_hsa_circ_54792,RMVar_hsa_circ_112935,RMVar_hsa_circ_123851,RMVar_hsa_circ_238609,RMVar_hsa_circ_238610,RMVar_hsa_circ_238611 113983 RMVar_ID_113983 Human_SNP_ID_864798917 m1A Human chr6 - 30703472 30703472 30703472 AGAGACCAGGCAGAGGAGGAGCCCAACAGAATACCAAGCCGCAGCCTCCGACGGACCAAACTTAA AGAGACCAGGCAGAGGAGGAGCCCAACAGAATGCCAAGCCGCAGCCTCCGACGGACCAAACTTAA T C MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:30703421..30703725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_252267,Human_RBP_ID_4879819,Human_RBP_ID_9400229,Human_RBP_ID_21322730,Human_RBP_ID_23059856,Human_RBP_ID_26353609 Human_Splice_Rec_749598,Human_Splice_Rec_749599,Human_Splice_Rec_749607 113984 RMVar_ID_113984 Human_SNP_ID_864808173 m1A Human chr6 + 132814739 132814738 132814740 ACAAGTCAATGCTTTTGTTTTTTAGTGCGTTCAAGATTCAACTTCACCCGTAACCCACCGCCATG ACAAGTCAATGCTTTTGTTTTTTAGTGCGTTC__GATTCAACTTCACCCGTAACCCACCGCCATG CAA C RPS12 Ensembl:ENSG00000112306 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:132814726..132815050 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 HNSC 1 - Human_RBP_ID_653349,Human_RBP_ID_1664090,Human_RBP_ID_2008682,Human_RBP_ID_2972389,Human_RBP_ID_4864503,Human_RBP_ID_5450463,Human_RBP_ID_5477354,Human_RBP_ID_8631127,Human_RBP_ID_9187955,Human_RBP_ID_17304679,Human_RBP_ID_17533631,Human_RBP_ID_18064197,Human_RBP_ID_22513256,Human_RBP_ID_22829519,Human_RBP_ID_24434851,Human_RBP_ID_24510136 Human_Splice_Rec_812584,Human_Splice_Rec_812585,Human_Splice_Rec_812594,Human_Splice_Rec_812595 RMVar_hsa_circ_80386,RMVar_hsa_circ_92431,RMVar_hsa_circ_109656,RMVar_hsa_circ_122890,RMVar_hsa_circ_102829,RMVar_hsa_circ_241576,RMVar_hsa_circ_241578,RMVar_hsa_circ_86524,RMVar_hsa_circ_241579,RMVar_hsa_circ_241577,RMVar_hsa_circ_314527,RMVar_hsa_circ_241575,RMVar_hsa_circ_297812,RMVar_hsa_circ_241580 113985 RMVar_ID_113985 Human_SNP_ID_864820829 m1A Human chr6 - 7592195 7592195 7592195 TTCTACACATGCTGTTGATGCTTCTTCCCCGCACCCGCCAACCCCCTAGCCAATTCAACTCACTT TTCTACACATGCTGTTGATGCTTCTTCCCCGCCCCCGCCAACCCCCTAGCCAATTCAACTCACTT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7592192..7592318 26863196 MeRIP-seq:(Medium) rs988129869 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 113986 RMVar_ID_113986 Human_SNP_ID_864825123 m1A Human chr6 + 29943364 29943364 29943364 GTACCGGCAGGACGCCTACGACGGCAAGGATTACATCGCCCTGAACGAGGACCTGCGCTCTTGGA GTACCGGCAGGACGCCTACGACGGCAAGGATTGCATCGCCCTGAACGAGGACCTGCGCTCTTGGA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:29943301..29943475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,colon adenocarcinoma,large_intestine adenocarcinoma 17 caecum,large intestine Human_RBP_ID_3805443,Human_RBP_ID_4878418,Human_RBP_ID_5617723,Human_RBP_ID_26541015,Human_RBP_ID_27161324 Human_Splice_Rec_747842,Human_Splice_Rec_747856,Human_Splice_Rec_747870,Human_Splice_Rec_747884,Human_Splice_Rec_747896,Human_Splice_Rec_747916 113987 RMVar_ID_113987 Human_SNP_ID_864841594 m1A Human chr6 - 31964015 31964015 31964015 ACTGGTGGTGAGGTCAAGGGAGGTGAGGCCTGAGGCCTGCTCATCACAGCGGCCCCGGGAGAAGG ACTGGTGGTGAGGTCAAGGGAGGTGAGGCCTGCGGCCTGCTCATCACAGCGGCCCCGGGAGAAGG T G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31963965..31964080 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary 113988 RMVar_ID_113988 Human_SNP_ID_864863007 m1A Human chr6 - 35367104 35367104 35367104 AGGTTCAAAGAATCAACCTCTTACACTCCTCCATTTCCTTTTAGCATCCAGGGAACGGACAAAAC AGGTTCAAAGAATCAACCTCTTACACTCCTCCGTTTCCTTTTAGCATCCAGGGAACGGACAAAAC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:35367098..35367206 26863196 MeRIP-seq:(Medium) rs149987507 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_7598465 113989 RMVar_ID_113989 Human_SNP_ID_864865696 m1A Human chr6 + 156935519 156935519 156935519 GGAACTAGATCTCAACCTCCTCTGGCCCCCGGAAAACCTAACCATGAAGACTTGAACTTAATACA GGAACTAGATCTCAACCTCCTCTGGCCCCCGGCAAACCTAACCATGAAGACTTGAACTTAATACA A C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:156935421..156935525;chr6:156935408..156935612 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_78947,Human_RBP_ID_2012312,Human_RBP_ID_3969388,Human_RBP_ID_8269765,Human_RBP_ID_9190133,Human_RBP_ID_9401329,Human_RBP_ID_18538922,Human_RBP_ID_24548652,Human_RBP_ID_27828115 Human_Splice_Rec_826970,Human_Splice_Rec_826971,Human_Splice_Rec_827006,Human_Splice_Rec_827007,Human_Splice_Rec_827044,Human_Splice_Rec_827045,Human_Splice_Rec_827080,Human_Splice_Rec_827081,Human_Splice_Rec_827116,Human_Splice_Rec_827117,Human_Splice_Rec_827126,Human_Splice_Rec_827127,Human_Splice_Rec_827150,Human_Splice_Rec_827160,Human_Splice_Rec_827161,Human_Splice_Rec_827196,Human_Splice_Rec_827197,Human_Splice_Rec_827204,Human_Splice_Rec_827205,Human_Splice_Rec_827208,Human_Splice_Rec_827209,Human_Splice_Rec_827229,Human_Splice_Rec_827239 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_108541,RMVar_hsa_circ_106096,RMVar_hsa_circ_242550,RMVar_hsa_circ_276425,RMVar_hsa_circ_242566,RMVar_hsa_circ_242567,RMVar_hsa_circ_338620,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_242574,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242575,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 113990 RMVar_ID_113990 Human_SNP_ID_864884330 m1A Human chr6 + 29945521 29945521 29945521 GTTGTTCCTGCCCTTCCCTTTGTGACTTGAAGAACCCTGACTTTGTTTCTGCAAAGGCACCTGCA GTTGTTCCTGCCCTTCCCTTTGTGACTTGAAGTACCCTGACTTTGTTTCTGCAAAGGCACCTGCA A T HLA-A Ensembl:ENSG00000206503 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29945426..29945710 26863196 MeRIP-seq:(Medium) rs1061235 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_660487,Human_RBP_ID_1113066,Human_RBP_ID_1670035,Human_RBP_ID_2017697,Human_RBP_ID_3002121,Human_RBP_ID_3805444,Human_RBP_ID_4878448,Human_RBP_ID_8641269,Human_RBP_ID_17663567,Human_RBP_ID_21221562,Human_RBP_ID_22405188,Human_RBP_ID_22461010,Human_RBP_ID_24155770,Human_RBP_ID_24512090,Human_RBP_ID_26534959,Human_RBP_ID_27094924 Human_Splice_Rec_747852,Human_Splice_Rec_747866,Human_Splice_Rec_747880,Human_Splice_Rec_747892,Human_Splice_Rec_747900,Human_Splice_Rec_747912 Human_miRNA_ID_728016 Clinvar_Rec_278,Clinvar_Rec_2415 GWAS_ID_8232,GWAS_ID_8233,GWAS_ID_8234 113991 RMVar_ID_113991 Human_SNP_ID_864908252 m1A Human chr6 + 73519367 73519367 73519367 ACCTGAGATGTCCCTGTAATCATGTTTTTGATAAAGTCTCTGTGTCCTGGGGCATCAATGATAGT ACCTGAGATGTCCCTGTAATCATGTTTTTGATGAAGTCTCTGTGTCCTGGGGCATCAATGATAGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:73519223..73519414 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,LICA,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 16 kidney,liver,large intestine 113992 RMVar_ID_113992 Human_SNP_ID_864914121 m1A Human chr6 + 7883176 7883176 7883176 CTAAAGTTCGTCTTTCGCTTGGCTCAGGACAAAGCGGTGTAACGAGTCAAGGTCTCTGCCTCCAC CTAAAGTTCGTCTTTCGCTTGGCTCAGGACAATGCGGTGTAACGAGTCAAGGTCTCTGCCTCCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:7883126..7883275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 113993 RMVar_ID_113993 Human_SNP_ID_864921459 m1A Human chr6 + 36985959 36985959 36985959 CCTCAGTGGTCGGGGCGTTGTCCCCAGACCCCAGGCCCCCTGACCCGCCATCCATCCTGCGGGCC CCTCAGTGGTCGGGGCGTTGTCCCCAGACCCCCGGCCCCCTGACCCGCCATCCATCCTGCGGGCC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:36985914..36986150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 113994 RMVar_ID_113994 Human_SNP_ID_864924038 m1A Human chr6 - 167951632 167951632 167951632 CGCTCCTCCTCCAGGCGGGCCTTCTCCTTCTCATACCAACGCTGATGTTCTTCTCTCTTTCTCCG CGCTCCTCCTCCAGGCGGGCCTTCTCCTTCTCGTACCAACGCTGATGTTCTTCTCTCTTTCTCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:167951585..167951722 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 113995 RMVar_ID_113995 Human_SNP_ID_864926066 m1A Human chr6 - 89654283 89654283 89654283 GCAACAGTCTGCAAAAGACTCTGGCAAAGATCAGGAAGAGGAGGAGATAGAGGACACCCTTATGG GCAACAGTCTGCAAAAGACTCTGGCAAAGATCGGGAAGAGGAGGAGATAGAGGACACCCTTATGG T C MDN1 Ensembl:ENSG00000112159 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr6:89654128..89654361;chr6:89654226..89654300;chr6:89654151..89654373;chr6:89654170..89654366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_8270290,Human_RBP_ID_18540038,Human_RBP_ID_26354214 Human_Splice_Rec_795100,Human_Splice_Rec_795302 RMVar_hsa_circ_26085,RMVar_hsa_circ_18844,RMVar_hsa_circ_123602,RMVar_hsa_circ_240232,RMVar_hsa_circ_43970,RMVar_hsa_circ_89443,RMVar_hsa_circ_124963,RMVar_hsa_circ_99918,RMVar_hsa_circ_55351,RMVar_hsa_circ_104524,RMVar_hsa_circ_240233,RMVar_hsa_circ_240234,RMVar_hsa_circ_240235,RMVar_hsa_circ_98408,RMVar_hsa_circ_266787,RMVar_hsa_circ_240236,RMVar_hsa_circ_114626,RMVar_hsa_circ_240237,RMVar_hsa_circ_70836,RMVar_hsa_circ_240238 113996 RMVar_ID_113996 Human_SNP_ID_864962204 m1A Human chr6 - 43130535 43130535 43130535 CATACCTCGCTACTACCACGTCCTGGGGTGCCAGCACCACCCTGGCAAAGCTTTCATCTGGAGAG CATACCTCGCTACTACCACGTCCTGGGGTGCCGGCACCACCCTGGCAAAGCTTTCATCTGGAGAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43130226..43130675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 8 stomach 113997 RMVar_ID_113997 Human_SNP_ID_864978010 m1A Human chr6 - 1611090 1611090 1611090 ATGTCCTGGATGCGCACGGGCGGCGGCTGCGGACCGGGCGCGTTGCCGTCGGCCTGCTCCGGCGG ATGTCCTGGATGCGCACGGGCGGCGGCTGCGGGCCGGGCGCGTTGCCGTCGGCCTGCTCCGGCGG T C lnc-GMDS-6,lnc-GMDS-6:2,lnc-GMDS-6:3,lnc-GMDS-6:4 RNACentral:URS0000D596A7,RNACentral:URS0000D6E293,RNACentral:URS00008B972B,RNACentral:URS00008B6C3C lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:1611001..1611300 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain 113998 RMVar_ID_113998 Human_SNP_ID_864990666 m1A Human chr6 - 85615020 85615020 85615020 AGAGGAGGTCCTGGATCAGCAAGAGGCGTTCGAGGTGCGAGAGGAGGTGCCCAACAACAAAGAGG AGAGGAGGTCCTGGATCAGCAAGAGGCGTTCGCGGTGCGAGAGGAGGTGCCCAACAACAAAGAGG T G SYNCRIP,AL589666.1 Ensembl:ENSG00000135316,Ensembl:ENSG00000271793 Protein coding,Protein coding CDS,CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:85614988..85615087 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma,large_intestine adenocarcinoma 27 head and neck,large intestine Human_RBP_ID_669611,Human_RBP_ID_791634,Human_RBP_ID_3817631,Human_RBP_ID_7639251,Human_RBP_ID_8650661,Human_RBP_ID_26354183 Human_Splice_Rec_792845,Human_Splice_Rec_792877,Human_Splice_Rec_792899 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063 113999 RMVar_ID_113999 Human_SNP_ID_864998880 m1A Human chr6 + 26156578 26156576 26156579 GGAGCGCAGCGGCGTATCTTTGGCCGCTCTCAAGAAAGCGCTGGCAGCCGCTGGCTATGACGTGG GGAGCGCAGCGGCGTATCTTTGGCCGCTCTC___AAAGCGCTGGCAGCCGCTGGCTATGACGTGG CAAG C lnc-HIST1H4D-3 RNACentral:URS0000D5AA68 lincRNA intron GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss DEL TCGA 32..34 33 HNSC 1 - Human_RBP_ID_7585697 RMVar_hsa_circ_237740,RMVar_hsa_circ_76721,RMVar_hsa_circ_237739 114000 RMVar_ID_114000 Human_SNP_ID_864999898 m1A Human chr6 - 36684153 36684145 36684153 CTCGCTGTCCACTGGGCCGAAGAGGCGGCGGCAGGCCTTGCTGCCGCATGGGTTCTGACGGACAT CTCGCTGTCCACTGGGCCGAAGAGGCGGCGGC________CTGCCGCATGGGTTCTGACGGACAT GCAAGGCCT G RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:36684074..36684254 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..40 33 BLCA 2 - 114001 RMVar_ID_114001 Human_SNP_ID_865022808 m1A Human chr6 - 29944596 29944596 29944596 CCCCTTCTCCACCTGAGCTCTTCCTCCTCCACATCACGGCAGCGACCACAGCTCCAGTGATCACA CCCCTTCTCCACCTGAGCTCTTCCTCCTCCACCTCACGGCAGCGACCACAGCTCCAGTGATCACA T G HCG4B RNACentral:URS00009B51D2 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:29944547..29944653 26863196 MeRIP-seq:(Medium) rs1137110 Functional Loss SNV ICGC,COSMIC 33..33 33 colon tubular,thyroid neoplasm,lung adenocarcinoma,LICA,large_intestine tubular,head_neck squamous_cell_carcinoma,lung large_cell_carcinoma 36 lung,head and neck,large intestine 114002 RMVar_ID_114002 Human_SNP_ID_865038564 m1A Human chr6 - 169751404 169751404 169751404 TGAAGTCGAGCCCCATCCAGACCCCGAACCAGACCCCTCAGCAGGCTCCGGTGACGCCTAGGAAA TGAAGTCGAGCCCCATCCAGACCCCGAACCAGTCCCCTCAGCAGGCTCCGGTGACGCCTAGGAAA T A TCTE3 Ensembl:ENSG00000184786 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:169751354..169751538 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_Splice_Rec_835301 114003 RMVar_ID_114003 Human_SNP_ID_865053899 m1A Human chr6 - 29942819 29942804 29942820 CTGCGTGTCGTCCACGTAGCCCACGGCGATGAAGCGGGGCTCCCCGCGGCCGGGCCGGGACACGG CTGCGTGTCGTCCACGTAGCCCACGGCGATG________________GGCCGGGCCGGGACACGG CGCGGGGAGCCCCGCTT C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:29942551..29943071 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..47 33 OV 1 - Human_RBP_ID_3822769 114004 RMVar_ID_114004 Human_SNP_ID_865117482 m1A Human chr6 + 15496606 15496606 15496606 CGGAGAAGCCGCAGTCGCCCCCCAAGAAGATGAAAGGGGCGGCTGGCCCCGCCGAAGGCCCTGGC CGGAGAAGCCGCAGTCGCCCCCCAAGAAGATGGAAGGGGCGGCTGGCCCCGCCGAAGGCCCTGGC A G JARID2 Ensembl:ENSG00000008083 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:15496559..15496767 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_3968563,Human_RBP_ID_8905102,Human_RBP_ID_9309102,Human_RBP_ID_22727967,Human_RBP_ID_27574244 Human_miRNA_ID_2397175,Human_miRNA_ID_2661596,Human_miRNA_ID_2680043,Human_miRNA_ID_2987671,Human_miRNA_ID_3010366,Human_miRNA_ID_3065556 RMVar_hsa_circ_50801,RMVar_hsa_circ_61103,RMVar_hsa_circ_19729,RMVar_hsa_circ_89803,RMVar_hsa_circ_266036,RMVar_hsa_circ_237259,RMVar_hsa_circ_23857,RMVar_hsa_circ_66832,RMVar_hsa_circ_337833,RMVar_hsa_circ_38132,RMVar_hsa_circ_322175,RMVar_hsa_circ_3965 114005 RMVar_ID_114005 Human_SNP_ID_865153414 m1A Human chr6 - 32128836 32128836 32128836 GCAACTGCTGACCTCAAGAAGGTGCTGGCGATAGATCCCAAAAACCGGGCAGCCCAGGAGGAACT GCAACTGCTGACCTCAAGAAGGTGCTGGCGATGGATCCCAAAAACCGGGCAGCCCAGGAGGAACT T C FKBPL Ensembl:ENSG00000204315 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32128786..32128864 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 114006 RMVar_ID_114006 Human_SNP_ID_865163644 m1A Human chr6 - 31900653 31900653 31900653 CATCTGCATCGTCAAGGTGGAGTCGGCCCTGGAGGTGGCACACCGGCTCAAACCCCCTGGAGGCC CATCTGCATCGTCAAGGTGGAGTCGGCCCTGGCGGTGGCACACCGGCTCAAACCCCCTGGAGGCC T G ZBTB12 Ensembl:ENSG00000204366 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31900603..31900699 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_27345813 114007 RMVar_ID_114007 Human_SNP_ID_865179871 m1A Human chr6 + 1313501 1313501 1313501 CCGCCAGGAGGAGCGCGCCAGCCCCGCGGGCAAGTTCTCCAGCTCCTTCGCCATCGACAGCATCC CCGCCAGGAGGAGCGCGCCAGCCCCGCGGGCAGGTTCTCCAGCTCCTTCGCCATCGACAGCATCC A G FOXQ1 Ensembl:ENSG00000164379 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:1313452..1313815 26863196 MeRIP-seq:(Medium) rs773920812 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 1 haematopoietic and lymphoid tissue 114008 RMVar_ID_114008 Human_SNP_ID_865202385 m1A Human chr6 + 33417520 33417520 33417520 TCTCCTTGGCGACCTTCTCGTTGGGGCAAGTAACAAAGGCTGCAGAGACCGAGCCCGGAACGTAG TCTCCTTGGCGACCTTCTCGTTGGGGCAAGTAGCAAAGGCTGCAGAGACCGAGCCCGGAACGTAG A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:33417516..33417925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 114009 RMVar_ID_114009 Human_SNP_ID_865213729 m1A Human chr6 - 27503140 27503140 27503140 TAAATTTCTTTCTTCTAAATTTTCTGTTGTTAATTATCTAAAACCTCGAACTCGTAGTCGGCAGG TAAATTTCTTTCTTCTAAATTTTCTGTTGTTAGTTATCTAAAACCTCGAACTCGTAGTCGGCAGG T C AL021918.3 Ensembl:ENSG00000285703 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27503100..27503230 26863196 MeRIP-seq:(Medium) rs1332802036 Functional Loss SNV ICGC 33..33 33 OV 1 - 114010 RMVar_ID_114010 Human_SNP_ID_865215728 m1A Human chr6 - 158789367 158789367 158789367 GCGTAATTTGTTTCATTCTGTTTTTCAGATCAATGTCCGAGTTACCACCATGGATGCAGAGCTGG GCGTAATTTGTTTCATTCTGTTTTTCAGATCAGTGTCCGAGTTACCACCATGGATGCAGAGCTGG T C EZR Ensembl:ENSG00000092820 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:158789276..158789375 26863196 MeRIP-seq:(Medium) rs144581330 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_79086,Human_RBP_ID_4908536,Human_RBP_ID_26828906 Human_Splice_Rec_828620,Human_Splice_Rec_828621,Human_Splice_Rec_828641,Human_Splice_Rec_828664,Human_Splice_Rec_828665,Human_Splice_Rec_828688,Human_Splice_Rec_828689 GWAS_ID_13427 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_125699,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_242786,RMVar_hsa_circ_298659,RMVar_hsa_circ_332275,RMVar_hsa_circ_19359,RMVar_hsa_circ_110280,RMVar_hsa_circ_242788,RMVar_hsa_circ_46193,RMVar_hsa_circ_242789 114011 RMVar_ID_114011 Human_SNP_ID_865237227 m1A Human chr6 + 31630800 31630800 31630800 GCCAGGCTGCGGATGAGGATGACAAGGGGATGAGGTGAGTCTTGGTCATGAGAAATGGGTGAGTT GCCAGGCTGCGGATGAGGATGACAAGGGGATGGGGTGAGTCTTGGTCATGAGAAATGGGTGAGTT A G PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:31630776..31630800;chr6:31630776..31630825 26863196 MeRIP-seq:(Medium) rs749871641 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach Human_RBP_ID_8900074,Human_RBP_ID_9309594 Human_Splice_Rec_752475,Human_Splice_Rec_752535 114012 RMVar_ID_114012 Human_SNP_ID_865237946 m1A Human chr6 + 99402624 99402624 99402624 AGCTTCCTGTTTTTGCCGGATTCGATGCCGTAATTCTTCATCATCAGTGTCAGATGACTCAGATC AGCTTCCTGTTTTTGCCGGATTCGATGCCGTAGTTCTTCATCATCAGTGTCAGATGACTCAGATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:99402573..99402678 26863196 MeRIP-seq:(Medium) rs367828524 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 114013 RMVar_ID_114013 Human_SNP_ID_865305030 m1A Human chr6 + 1611095 1611088 1611095 GGAGCAGGCCGACGGCAACGCGCCCGGTCCGCAGCCGCCGCCCGTGCGCATCCAGGACATCAAGA GGAGCAGGCCGACGGCAACGCGCCCG_______GCCGCCGCCCGTGCGCATCCAGGACATCAAGA GGTCCGCA G FOXC1 Ensembl:ENSG00000054598 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:1611049..1611184 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 27..33 33 SKCM 1 - Human_RBP_ID_7568527,Human_RBP_ID_27520917 114014 RMVar_ID_114014 Human_SNP_ID_865305817 m1A Human chr6 + 36489795 36489795 36489795 TTGATATTTTAGCCAGAGAAATCGGCAAGCCAAGATTAACCCGAATCTGAAGTTTAGAATCTTGA TTGATATTTTAGCCAGAGAAATCGGCAAGCCATGATTAACCCGAATCTGAAGTTTAGAATCTTGA A T KCTD20 Ensembl:ENSG00000112078 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36489745..36489845 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_8216529,Human_RBP_ID_18085349,Human_RBP_ID_26540032 114015 RMVar_ID_114015 Human_SNP_ID_865314577 m1A Human chr6 - 29887990 29887989 29887990 GATGAAGCGGGGCTCCCCGCGGCCGGGCCGGGACATGGTGGTGTAGAAATACCTCATGGAGTGGG GATGAAGCGGGGCTCCCCGCGGCCGGGCCGGG_CATGGTGGTGTAGAAATACCTCATGGAGTGGG GT G AL645929.1 Ensembl:ENSG00000230521 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:29887853..29888050 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BRCA 1 - Human_RBP_ID_3822774 114016 RMVar_ID_114016 Human_SNP_ID_865334130 m1A Human chr6 + 134170383 134170383 134170383 CGCTGTCAGGGGACTTGCCAATGGAGTTGGGGACAGGCTCTTCGGTAAACTCGGGGTCAAAGTGC CGCTGTCAGGGGACTTGCCAATGGAGTTGGGGGCAGGCTCTTCGGTAAACTCGGGGTCAAAGTGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:134170159..134170470 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 114017 RMVar_ID_114017 Human_SNP_ID_865337961 m1A Human chr6 + 43624551 43624551 43624551 TGAGCAAACTGCTGGGCAGCAGTGACGGCATCATCCTCAGAGGTGACCAGCATGGGGACCTTGTG TGAGCAAACTGCTGGGCAGCAGTGACGGCATCCTCCTCAGAGGTGACCAGCATGGGGACCTTGTG A C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:43623926..43625513;chr6:43623926..43627013 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach 114018 RMVar_ID_114018 Human_SNP_ID_865392284 m1A Human chr6 - 46652683 46652683 46652683 TACGAAGGAGAGCTGCAAAAGTTGCAGCAGAAAGGTTGGGAGTCCCGACAGGTTCCGTAGCCCAC TACGAAGGAGAGCTGCAAAAGTTGCAGCAGAAGGGTTGGGAGTCCCGACAGGTTCCGTAGCCCAC T C CYP39A1 Ensembl:ENSG00000146233 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:46652632..46652741 26863196 MeRIP-seq:(Medium) rs555227266 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver 114019 RMVar_ID_114019 Human_SNP_ID_865408075 m1A Human chr6 - 30743769 30743754 30743770 CACCCGGTGCTTGAGGCGGGACCGAGGCGCACAGAGACCGAGGCGCATAGAGACCGAGGCACAGC CACCCGGTGCTTGAGGCGGGACCGAGGCGCA________________TAGAGACCGAGGCACAGC ATGCGCCTCGGTCTCTG A IER3 Ensembl:ENSG00000137331 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:30743718..30743850 26863196 MeRIP-seq:(Medium) rs1424846488 Functional Loss DEL TCGA 32..47 33 ESCA 1 - Human_RBP_ID_17537855,Human_RBP_ID_22104821,Human_RBP_ID_27523057 114020 RMVar_ID_114020 Human_SNP_ID_865410881 m1A Human chr6 - 36598954 36598954 36598954 TACCTGCGACGAGGTGGAGGACTCCTCCTACGATAATCATCTCGAGGGCGACGACCCCAAGAGGG TACCTGCGACGAGGTGGAGGACTCCTCCTACGTTAATCATCTCGAGGGCGACGACCCCAAGAGGG T A RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:36598502..36599528 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 114021 RMVar_ID_114021 Human_SNP_ID_865412872 m1A Human chr6 + 43624908 43624908 43624908 AATGCCTCGTACCAATCCCAGTGTTGGCACTGACGAGGAGCAGGGCGCAGTCGGGGCAGTATGAT AATGCCTCGTACCAATCCCAGTGTTGGCACTGTCGAGGAGCAGGGCGCAGTCGGGGCAGTATGAT A T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:43624901..43625002 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 114022 RMVar_ID_114022 Human_SNP_ID_865422792 m1A Human chr6 + 31530378 31530378 31530378 GGGGTGGGGGCAGTAGTGTCTCCTTCACCCCCACCCTGGTGTCCTCTCCTGAAGGACAGACGGTC GGGGTGGGGGCAGTAGTGTCTCCTTCACCCCCGCCCTGGTGTCCTCTCCTGAAGGACAGACGGTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:31530276..31530475 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 114023 RMVar_ID_114023 Human_SNP_ID_865438029 m1A Human chr6 - 7883264 7883264 7883264 TTTGCAAACTTTTTTCTTTTTTGTTTTAAGGTACGAGGCTACCCCACGTTATTGCTTTTCCGAGG TTTGCAAACTTTTTTCTTTTTTGTTTTAAGGTGCGAGGCTACCCCACGTTATTGCTTTTCCGAGG T C BLOC1S5-TXNDC5,TXNDC5 Ensembl:ENSG00000259040,Ensembl:ENSG00000239264 Protein coding,Protein coding 3'UTR,exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:7883201..7884475 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_18084687,Human_RBP_ID_22773245,Human_RBP_ID_26827854 Human_Splice_Rec_736206,Human_Splice_Rec_736224,Human_Splice_Rec_736242,Human_Splice_Rec_736248,Human_Splice_Rec_736274 114024 RMVar_ID_114024 Human_SNP_ID_865452924 m1A Human chr6 - 70413579 70413579 70413579 TCCCGCCCCGGGCCCCCTCACATCGCCATCACAGCAACCGCAAACACCGCAACCGCGGAGCCGGT TCCCGCCCCGGGCCCCCTCACATCGCCATCACCGCAACCGCAAACACCGCAACCGCGGAGCCGGT T G FAM135A-AS1 Ensembl:ENSG00000224349 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr6:70413536..70413658;chr6:70413528..70413750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114025 RMVar_ID_114025 Human_SNP_ID_865455070 m1A Human chr6 + 139373398 139373374 139373398 GCCGCTGTTGCTGCTGCCCGCGCCGCCGCCCGAGCTGCTGCCAGAGCCGCCGGGGGTGCTGCTGC GCCGCTGTT________________________GCTGCTGCCAGAGCCGCCGGGGGTGCTGCTGC TGCTGCTGCCCGCGCCGCCGCCCGA T AL592429.2 Ensembl:ENSG00000226571 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:139373348..139374172 26863196 MeRIP-seq:(Medium) rs780870084 Functional Loss DEL ICGC 10..33 33 COCA 1 - 114026 RMVar_ID_114026 Human_SNP_ID_865470622 m1A Human chr6 - 122399732 122399732 122399732 AGCCGGCACGTTCGAACTCTGCTTCATTGTTAACGCGGCGCAGGGATTCCAAATTCTACACCCGA AGCCGGCACGTTCGAACTCTGCTTCATTGTTACCGCGGCGCAGGGATTCCAAATTCTACACCCGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:122399683..122399781 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck 114027 RMVar_ID_114027 Human_SNP_ID_865471975 m1A Human chr6 + 30577882 30577882 30577882 GGCTGGGGAAGAAGAGAAAGTGCTCAAGGAGAAGGAGCAGCAGCAGCAGCAACAGCAACAGCAGG GGCTGGGGAAGAAGAGAAAGTGCTCAAGGAGAGGGAGCAGCAGCAGCAGCAACAGCAACAGCAGG A G ABCF1 Ensembl:ENSG00000204574 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:30577801..30578110 26863196 MeRIP-seq:(Medium) rs1404226235 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung Human_RBP_ID_5152061,Human_RBP_ID_8237584,Human_RBP_ID_9400173,Human_RBP_ID_18413831,Human_RBP_ID_23059755,Human_RBP_ID_24178818,Human_RBP_ID_24548363,Human_RBP_ID_26353140,Human_RBP_ID_27827422 Human_Splice_Rec_748892,Human_Splice_Rec_748893,Human_Splice_Rec_748938,Human_Splice_Rec_748939,Human_Splice_Rec_748956,Human_Splice_Rec_748957,Human_Splice_Rec_748970,Human_Splice_Rec_748971 114028 RMVar_ID_114028 Human_SNP_ID_865474408 m1A Human chr6 - 85490568 85490568 85490568 AGGCCTTCTTCAGGGTGGAACCTTTTAACTGGACTAGGTCAAATGTGCCTCCAAAGGGCAATACA AGGCCTTCTTCAGGGTGGAACCTTTTAACTGGGCTAGGTCAAATGTGCCTCCAAAGGGCAATACA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:85487448..85491086 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary 114029 RMVar_ID_114029 Human_SNP_ID_865480815 m1A Human chr6 + 43369155 43369155 43369155 GGACGGGGAGACGCGACGACCCCGTGGCGGGGACGGCGAGGCCCGGCGGCCGCGGTGCCCTGAGG GGACGGGGAGACGCGACGACCCCGTGGCGGGGGCGGCGAGGCCCGGCGGCCGCGGTGCCCTGAGG A G RF00017-4495,RF00017-4633 RNACentral:URS0000923EDC,RNACentral:URS00009644F0 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:43369043..43369450 26863196 MeRIP-seq:(Medium) rs920540474 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 114030 RMVar_ID_114030 Human_SNP_ID_865481563 m1A Human chr6 + 43451126 43451126 43451126 GAGGCAGGAGAAGCGGTTTATGCCGTCAAGGCAGGTGGCACCGTTAGCACAAGGCCGCATCAGGC GAGGCAGGAGAAGCGGTTTATGCCGTCAAGGCGGGTGGCACCGTTAGCACAAGGCCGCATCAGGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43451076..43453129 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114031 RMVar_ID_114031 Human_SNP_ID_865483868 m1A Human chr6 - 29628307 29628307 29628307 CGTGCTTCAGCCTCCCGCGGCTCCCTCCGCCCACCCCGCCCTCCTGGCACGCCCCGTCCCCATTT CGTGCTTCAGCCTCCCGCGGCTCCCTCCGCCCCCCCCGCCCTCCTGGCACGCCCCGTCCCCATTT T G GABBR1 Ensembl:ENSG00000204681 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:29627853..29628594 26863196 MeRIP-seq:(Medium) rs1377337687 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_17576618 114032 RMVar_ID_114032 Human_SNP_ID_865490474 m1A Human chr6 + 36981614 36981614 36981614 ACTCACCGTAGGTGAAGAAGCTCGGCAGATAGAGGACCTTCCTCCCCAGCACATTGGTCCCAAGG ACTCACCGTAGGTGAAGAAGCTCGGCAGATAGGGGACCTTCCTCCCCAGCACATTGGTCCCAAGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:36981601..36981675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 114033 RMVar_ID_114033 Human_SNP_ID_865501190 m1A Human chr6 + 161225176 161225176 161225176 TTCCGATGACCTGCTCCACCCTGACTCATTCCAATTACCTACTCTACCCTGACTCATTCTGATTC TTCCGATGACCTGCTCCACCCTGACTCATTCCGATTACCTACTCTACCCTGACTCATTCTGATTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:161224986..161225217 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114034 RMVar_ID_114034 Human_SNP_ID_865529267 m1A Human chr6 + 42888216 42888216 42888216 TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTG TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCGTGATCTCAGCTCATTGCAGCCTCCACCTCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878875910 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_252300,Human_RBP_ID_664709 114035 RMVar_ID_114035 Human_SNP_ID_865554809 m1A Human chr6 + 31634285 31634270 31634285 TCATAGCTCTGGATTCTTGGGCTCTAAGCCTGAGGGCCCAGGCCCTCAGGCAGAGTCCAGAGATA TCATAGCTCTGGATTCTT_______________GGGCCCAGGCCCTCAGGCAGAGTCCAGAGATA TGGGCTCTAAGCCTGA T PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31634226..31634439 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 19..33 33 BLCA 1 - Human_RBP_ID_661502,Human_RBP_ID_3968719,Human_RBP_ID_8905237,Human_RBP_ID_9309609,Human_RBP_ID_27523387 Human_Splice_Rec_752482,Human_Splice_Rec_752483,Human_Splice_Rec_752542,Human_Splice_Rec_752543,Human_Splice_Rec_752589 114036 RMVar_ID_114036 Human_SNP_ID_865583794 m1A Human chr6 + 34245206 34245206 34245206 ACTTAGCCGCACCCTGCACCTGCTGCGTCCCCACTCCCTTGGTGGTGGGGACATTGCTCTCTGGG ACTTAGCCGCACCCTGCACCTGCTGCGTCCCCCCTCCCTTGGTGGTGGGGACATTGCTCTCTGGG A C HMGA1 Ensembl:ENSG00000137309 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34245156..34245286 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas Human_RBP_ID_662758,Human_RBP_ID_790407,Human_RBP_ID_1217470,Human_RBP_ID_17091451,Human_RBP_ID_17306787,Human_RBP_ID_17421609,Human_RBP_ID_17537879,Human_RBP_ID_18074614,Human_RBP_ID_21221757,Human_RBP_ID_27161171,Human_RBP_ID_27527021 Human_miRNA_ID_96891,Human_miRNA_ID_1421218,Human_miRNA_ID_2725207 RMVar_hsa_circ_126239,RMVar_hsa_circ_237945 114037 RMVar_ID_114037 Human_SNP_ID_865603925 m1A Human chr6 - 116279463 116279463 116279463 TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAAGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAGGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA T C TSPYL1 Ensembl:ENSG00000189241 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:116279251..116279562 26863196 MeRIP-seq:(Medium) rs1034648999 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,ESCA,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_1324070,Human_RBP_ID_18852236 114038 RMVar_ID_114038 Human_SNP_ID_865606125 m1A Human chr6 - 31645445 31645445 31645445 TGCATGTGGTCCGGCCTATGTCTCACTACACCACCCCCATGGTGCTCCAGCAGGCAGCCATTCCC TGCATGTGGTCCGGCCTATGTCTCACTACACCGCCCCCATGGTGCTCCAGCAGGCAGCCATTCCC T C BAG6 Ensembl:ENSG00000204463 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31645426..31645450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_1046880,Human_RBP_ID_1326901,Human_RBP_ID_8642236,Human_RBP_ID_9308261,Human_RBP_ID_17306569,Human_RBP_ID_17419665,Human_RBP_ID_18195446,Human_RBP_ID_18863016,Human_RBP_ID_24157140,Human_RBP_ID_27345626,Human_RBP_ID_27523421 Human_Splice_Rec_752659,Human_Splice_Rec_752707,Human_Splice_Rec_752753,Human_Splice_Rec_752801,Human_Splice_Rec_752847,Human_Splice_Rec_752903,Human_Splice_Rec_752929,Human_Splice_Rec_752935,Human_Splice_Rec_752959 114039 RMVar_ID_114039 Human_SNP_ID_865630437 m1A Human chr6 + 165958344 165958344 165958344 AAAGCCAAAACCAGCAGTTACAAATAATTACCACTTGGCCTACAATTTCAAAAGAAAGTTGGAGA AAAGCCAAAACCAGCAGTTACAAATAATTACCTCTTGGCCTACAATTTCAAAAGAAAGTTGGAGA A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165958326..165958350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114040 RMVar_ID_114040 Human_SNP_ID_865631295 m1A Human chr6 - 134170401 134170401 134170401 TGGGCCCAACGACCTACGGCACTTTGACCCCGAGTTTACCGAAGAGCCTGTCCCCAACTCCATTG TGGGCCCAACGACCTACGGCACTTTGACCCCGGGTTTACCGAAGAGCCTGTCCCCAACTCCATTG T C SGK1 Ensembl:ENSG00000118515 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:134170376..134170400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 14 large intestine Human_RBP_ID_79885,Human_RBP_ID_5216950,Human_RBP_ID_15651605,Human_RBP_ID_22619192,Human_RBP_ID_24562414,Human_RBP_ID_26039365,Human_RBP_ID_27519501 Human_Splice_Rec_813268,Human_Splice_Rec_813292,Human_Splice_Rec_813302,Human_Splice_Rec_813324,Human_Splice_Rec_813344,Human_Splice_Rec_813364,Human_Splice_Rec_813386,Human_Splice_Rec_813406 RMVar_hsa_circ_85452,RMVar_hsa_circ_241602 114041 RMVar_ID_114041 Human_SNP_ID_865661984 m1A Human chr6 + 33313273 33313273 33313273 GCTCCTGCTGAGGCTCTGGCTGTGGTCGCAAGAGGCTGGAGAGGCTGAGGACTGGGCTGGATATG GCTCCTGCTGAGGCTCTGGCTGTGGTCGCAAGCGGCTGGAGAGGCTGAGGACTGGGCTGGATATG A C RF00017-4596 RNACentral:URS0000934741 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33313189..33313421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 114042 RMVar_ID_114042 Human_SNP_ID_865664087 m1A Human chr6 - 26056079 26056079 26056079 ACTCAACAAGAAGGCAGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAAAGGCGGGCGGAACCAAAC ACTCAACAAGAAGGCAGCCTCCGGGGAAGCCAGGCCCAAGGTTAAAAAGGCGGGCGGAACCAAAC T C H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26055976..26056200 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_658977,Human_RBP_ID_948548,Human_RBP_ID_1045984,Human_RBP_ID_1326431,Human_RBP_ID_1668818,Human_RBP_ID_2016674,Human_RBP_ID_3804145,Human_RBP_ID_4876069,Human_RBP_ID_8639977,Human_RBP_ID_9192811,Human_RBP_ID_9400058,Human_RBP_ID_9444294,Human_RBP_ID_18860536,Human_RBP_ID_22102274,Human_RBP_ID_22309190,Human_RBP_ID_22460429,Human_RBP_ID_22772629,Human_RBP_ID_22830329,Human_RBP_ID_24387602,Human_RBP_ID_26353471,Human_RBP_ID_26714191,Human_RBP_ID_27093640,Human_RBP_ID_27343946,Human_RBP_ID_27521852 RMVar_hsa_circ_266433 114043 RMVar_ID_114043 Human_SNP_ID_865680539 m1A Human chr6 - 30712375 30712375 30712375 GAAGCCAAGCCTCCACCACAGTGGACATCAACACACAAGTGGAGAAGGAAGTCCCGCCAGGGTCA GAAGCCAAGCCTCCACCACAGTGGACATCAACTCACAAGTGGAGAAGGAAGTCCCGCCAGGGTCA T A MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:30712351..30712375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_8899825,Human_RBP_ID_17306385 RMVar_hsa_circ_66652,RMVar_hsa_circ_268062 114044 RMVar_ID_114044 Human_SNP_ID_865720015 m1A Human chr6 - 43014301 43014265 43014301 GGGGCGGGGCCGCGGGTCCTCGAGCTGCCTGCAGCCTAGAACCCGTTGCGCGCCAACCGACGCCT GGGGCGGGGCCGCGGGTCCTCGAGCTGCCTGC_________________________________ ACTAAGGCGTCGGTTGGCGCGCAACGGGTTCTAGGCT A MEA1 Ensembl:ENSG00000124733 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr6:43014251..43017225;chr6:43014251..43014404 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..65 33 OV 1 - 114045 RMVar_ID_114045 Human_SNP_ID_865722465 m1A Human chr6 - 139373632 139373632 139373632 ACAACTCCCAGTTCATGGGTCCCCCGGTGGCCAGCCAGGGAGGCTCCCTGCCGGCCAGCATGCAG ACAACTCCCAGTTCATGGGTCCCCCGGTGGCCTGCCAGGGAGGCTCCCTGCCGGCCAGCATGCAG T A CITED2 Ensembl:ENSG00000164442 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:139373324..139373645 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_252350,Human_RBP_ID_947906,Human_RBP_ID_7550870,Human_RBP_ID_22105414,Human_RBP_ID_22460809 114046 RMVar_ID_114046 Human_SNP_ID_865723445 m1A Human chr6 - 43629066 43629066 43629066 GCGGAACCCTCAAGGCTAGGGGGGCCGGCAGCAGCAGCGGCTGCGGGGGGCCAAAGGGAAAGAAG GCGGAACCCTCAAGGCTAGGGGGGCCGGCAGCTGCAGCGGCTGCGGGGGGCCAAAGGGAAAGAAG T A GTPBP2 Ensembl:ENSG00000172432 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:43629027..43629200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_13463,Human_RBP_ID_215467,Human_RBP_ID_252384,Human_RBP_ID_949692,Human_RBP_ID_1678571,Human_RBP_ID_3969150,Human_RBP_ID_5398894,Human_RBP_ID_5478537,Human_RBP_ID_9336178,Human_RBP_ID_9437472,Human_RBP_ID_18425659,Human_RBP_ID_19018721,Human_RBP_ID_21991757,Human_RBP_ID_23067367,Human_RBP_ID_24164272,Human_RBP_ID_24554636,Human_RBP_ID_26355216 Human_Splice_Rec_773655,Human_Splice_Rec_773695 114047 RMVar_ID_114047 Human_SNP_ID_865740819 m1A Human chr6 - 43517150 43517150 43517150 TTACATTGCGAACCCCAAACTCCCCCAGAACCACGCGGCTCCGCATTTCCTCCACCGCCTGAGAA TTACATTGCGAACCCCAAACTCCCCCAGAACCCCGCGGCTCCGCATTTCCTCCACCGCCTGAGAA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:43517101..43517230;chr6:43517101..43517310 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 2 - 114048 RMVar_ID_114048 Human_SNP_ID_865743042 m1A Human chr6 - 31629250 31629250 31629250 CCCAAGCCCTGACTAGGGGGCTGGCGGGTGGGACCAATCCCATCACCCTTGGGTTCCACCTTTGG CCCAAGCCCTGACTAGGGGGCTGGCGGGTGGGGCCAATCCCATCACCCTTGGGTTCCACCTTTGG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:31629226..31629250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114049 RMVar_ID_114049 Human_SNP_ID_865751150 m1A Human chr6 + 31557728 31557728 31557728 GGGGAGACCCCTGGCCAAATTTTGGGCTGGGGACCCCCCTGGGATTCTGCTGAAGAGGAGGAAGA GGGGAGACCCCTGGCCAAATTTTGGGCTGGGGCCCCCCCTGGGATTCTGCTGAAGAGGAGGAAGA A C NFKBIL1 Ensembl:ENSG00000204498 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31557679..31557878 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_661435,Human_RBP_ID_8899987 Human_Splice_Rec_752225 114050 RMVar_ID_114050 Human_SNP_ID_865776922 m1A Human chr6 + 143195696 143195696 143195696 AGGGAGCCCTCGCCAGGGAGGGAGAATATCTTAGGGAGGAGGAGTGCAGGGTAGCTGAGGAGAGC AGGGAGCCCTCGCCAGGGAGGGAGAATATCTTTGGGAGGAGGAGTGCAGGGTAGCTGAGGAGAGC A T AIG1 Ensembl:ENSG00000146416 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:143195428..143195736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_7552670,Human_RBP_ID_9438217,Human_RBP_ID_17663434,Human_RBP_ID_23294984 RMVar_hsa_circ_276893,RMVar_hsa_circ_352387,RMVar_hsa_circ_336189,RMVar_hsa_circ_241895 114051 RMVar_ID_114051 Human_SNP_ID_865797423 m1A Human chr6 - 31889301 31889301 31889301 AGTGGCCGGCGCAAGGCCAAGAAGAAATGGCGAAAAGACAGCCCATGGGTGAAGCCGTCTCGGAA AGTGGCCGGCGCAAGGCCAAGAAGAAATGGCGGAAAGACAGCCCATGGGTGAAGCCGTCTCGGAA T C EHMT2 Ensembl:ENSG00000204371 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31889251..31889377 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 4 head and neck Human_RBP_ID_1678488,Human_RBP_ID_3968839,Human_RBP_ID_5532372,Human_RBP_ID_9400298,Human_RBP_ID_19016717,Human_RBP_ID_22104906,Human_RBP_ID_23067328,Human_RBP_ID_23120274,Human_RBP_ID_24548378,Human_RBP_ID_26353161,Human_RBP_ID_27827495 Human_Splice_Rec_755110,Human_Splice_Rec_755111,Human_Splice_Rec_755162,Human_Splice_Rec_755163,Human_Splice_Rec_755214,Human_Splice_Rec_755215,Human_Splice_Rec_755266,Human_Splice_Rec_755267,Human_Splice_Rec_755318,Human_Splice_Rec_755319 114052 RMVar_ID_114052 Human_SNP_ID_865822900 m1A Human chr6 + 26199749 26199749 26199749 CGGCATCTCATCCAAGGCCATGGGCATCATGAACTCCTTCGTCAACGATATCTTCGAGCGCATCG CGGCATCTCATCCAAGGCCATGGGCATCATGAGCTCCTTCGTCAACGATATCTTCGAGCGCATCG A G H2BC7 Ensembl:ENSG00000277224 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26199619..26199869 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_792285,Human_RBP_ID_1668956,Human_RBP_ID_18195341,Human_RBP_ID_22461680,Human_RBP_ID_24511902,Human_RBP_ID_26534490,Human_RBP_ID_26827984 114053 RMVar_ID_114053 Human_SNP_ID_865832696 m1A Human chr6 + 158787166 158787166 158787166 GAAATCCTTTATTATCCACATAGTGGAGGCCAAAGTACCACACTTCCCGGAGGCCGATAGTCTTT GAAATCCTTTATTATCCACATAGTGGAGGCCACAGTACCACACTTCCCGGAGGCCGATAGTCTTT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:158787101..158787175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 CHOL 1 - 114054 RMVar_ID_114054 Human_SNP_ID_865840046 m1A Human chr6 + 43051022 43051022 43051022 TTGCTCTGCCGAAACTCGCCCTCATCCCCGGCACTGATCTCCTCATAATCATCCAGCATCCGCAC TTGCTCTGCCGAAACTCGCCCTCATCCCCGGCCCTGATCTCCTCATAATCATCCAGCATCCGCAC A C KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:43050951..43051071 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_18866121 114055 RMVar_ID_114055 Human_SNP_ID_865846600 m1A Human chr6 - 27146583 27146583 27146583 ATCATGAACTCCTTCGTCAACGACATCTTCGAACGCATCGCGGGTGAGGCTTCCCGCCTGGCGCA ATCATGAACTCCTTCGTCAACGACATCTTCGAGCGCATCGCGGGTGAGGCTTCCCGCCTGGCGCA T C H2BC12 Ensembl:ENSG00000197903 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:27146535..27146615 26863196 MeRIP-seq:(Medium) rs758323873 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_81124,Human_RBP_ID_251758,Human_RBP_ID_659588,Human_RBP_ID_1046201,Human_RBP_ID_1669249,Human_RBP_ID_2016970,Human_RBP_ID_3804563,Human_RBP_ID_7586728,Human_RBP_ID_8640412,Human_RBP_ID_8899282,Human_RBP_ID_15771770,Human_RBP_ID_18195347,Human_RBP_ID_18369608,Human_RBP_ID_18449973,Human_RBP_ID_18538989,Human_RBP_ID_18860987,Human_RBP_ID_22460504,Human_RBP_ID_22513809,Human_RBP_ID_26353503,Human_RBP_ID_26828046,Human_RBP_ID_27522185 Human_miRNA_ID_3003569,Human_miRNA_ID_3003570 RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 114056 RMVar_ID_114056 Human_SNP_ID_865858477 m1A Human chr6 - 148878612 148878612 148878612 ACTCATACACGATCTCCACACTCATACACGACACCCACACTAATACACGACCCCCGCACTCATAC ACTCATACACGATCTCCACACTCATACACGACCCCCACACTAATACACGACCCCCGCACTCATAC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:148878593..148878720 26863196 MeRIP-seq:(Medium) rs1279137921 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114057 RMVar_ID_114057 Human_SNP_ID_865861609 m1A Human chr6 - 61574218 61574218 61574218 GTCACTGGGCAGGCGGTGCCTCTAATACTGGTAATGCTAGAGGTGATGTTTTTGGTAAACAGGCG GTCACTGGGCAGGCGGTGCCTCTAATACTGGTGATGCTAGAGGTGATGTTTTTGGTAAACAGGCG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:61574123..61574370 26863410 MeRIP-seq:(Medium) rs62424615 Functional Loss SNV ICGC 33..33 33 LICA 5 - RMVar_hsa_circ_32927,RMVar_hsa_circ_346489,RMVar_hsa_circ_26123 114058 RMVar_ID_114058 Human_SNP_ID_865880314 m1A Human chr6 + 26216545 26216545 26216545 TTGTACACATACACGGAGTAGCTCTCCTTACGACTGCGCTTGCGCTTCTTGCCATCCTTCTTCTG TTGTACACATACACGGAGTAGCTCTCCTTACGGCTGCGCTTGCGCTTCTTGCCATCCTTCTTCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:26216526..26216550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 114059 RMVar_ID_114059 Human_SNP_ID_865916010 m1A Human chr6 + 89721526 89721526 89721526 CCCTGTGTGGAGCAAGTTTTAAAGAAGCAAAGAACTCAGAATTCATGCTTGAAGAAATGCAGGCA CCCTGTGTGGAGCAAGTTTTAAAGAAGCAAAGGACTCAGAATTCATGCTTGAAGAAATGCAGGCA A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878986217 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,BRCA,breast ductal_carcinoma 5 lung,breast 114060 RMVar_ID_114060 Human_SNP_ID_865925492 m1A Human chr6 - 31271655 31271655 31271655 CCGGGAGACACAGAAGTACAAGCGCCAGGCACAGGCTGACCGAGTGAGCCTGCGGAACCTGCGCG CCGGGAGACACAGAAGTACAAGCGCCAGGCACGGGCTGACCGAGTGAGCCTGCGGAACCTGCGCG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_8641900,Human_RBP_ID_22773385 Human_Splice_Rec_751699,Human_Splice_Rec_751713,Human_Splice_Rec_751727,Human_Splice_Rec_751741,Human_Splice_Rec_751753,Human_Splice_Rec_751757 114061 RMVar_ID_114061 Human_SNP_ID_865937933 m1A Human chr6 + 150143220 150143220 150143220 GGGACATGTCGGTGGCGACGGGCAGCAGCGAGACGGCCGGCGGGGCCAGCGGCGGCGGCGCACGG GGGACATGTCGGTGGCGACGGGCAGCAGCGAGGCGGCCGGCGGGGCCAGCGGCGGCGGCGCACGG A G PPP1R14C Ensembl:ENSG00000198729 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:150143124..150143369 26863410 MeRIP-seq:(Medium) rs2297672 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 7 head and neck 114062 RMVar_ID_114062 Human_SNP_ID_865959836 m1A Human chr6 - 31827847 31827847 31827847 AGCTCAGTCCTTCGGAACGCCGGAAACTCAACACGCCGGTGCCTGCAGCCGCACAGGTTCGCTCT AGCTCAGTCCTTCGGAACGCCGGAAACTCAACGCGCCGGTGCCTGCAGCCGCACAGGTTCGCTCT T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr6:31827769..31827919;chr6:31827751..31828000 26863196,32194978 MeRIP-seq:(Medium) rs2607020 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 114063 RMVar_ID_114063 Human_SNP_ID_865969024 m1A Human chr6 + 31280505 31280505 31280505 ATGACCCACATCGTGCGGGAAGTCGACAGGCCAGGATCCAAGGTGAACAAGAAGGAGGTGGTGGA ATGACCCACATCGTGCGGGAAGTCGACAGGCCGGGATCCAAGGTGAACAAGAAGGAGGTGGTGGA A G RPL3P2 Ensembl:ENSG00000227939 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879023901 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_4911480,Human_RBP_ID_8270520,Human_RBP_ID_26541064,Human_RBP_ID_27095750 114064 RMVar_ID_114064 Human_SNP_ID_865983092 m1A Human chr6 + 165749459 165749457 165749460 ACCACCATCACCATCACCACCATCACATCACCATCATCAACAACACCATCAACACCATCATCACC ACCACCATCACCATCACCACCATCACATCAC___CATCAACAACACCATCAACACCATCATCACC CCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165749184..165749493 26863196 MeRIP-seq:(Medium) rs1325000220 Functional Loss DEL ICGC 32..34 33 PAAD 1 - 114065 RMVar_ID_114065 Human_SNP_ID_865989210 m1A Human chr6 + 7282293 7282293 7282293 AAAAACAACAGAACAGGAAGTGAGGCAGGAGAACCACAGAGATGGAAGCCAGGAGGTGTCCAATT AAAAACAACAGAACAGGAAGTGAGGCAGGAGAGCCACAGAGATGGAAGCCAGGAGGTGTCCAATT A G AL139095.4 Ensembl:ENSG00000238221 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:7282243..7282344 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114066 RMVar_ID_114066 Human_SNP_ID_865997792 m1A Human chr6 - 44249415 44249415 44249415 ATTTTCAGCTCTTTACCACTGTCCAACTTCGAAGGGTCTGTCAGGCTCTCATAGCGAATCTTGTC ATTTTCAGCTCTTTACCACTGTCCAACTTCGATGGGTCTGTCAGGCTCTCATAGCGAATCTTGTC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:44249378..44249586 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 testis teratoma 4 testis 114067 RMVar_ID_114067 Human_SNP_ID_866004073 m1A Human chr6 + 150876134 150876133 150876134 GAATTCAAAAGAAGTTCTAAGTTTATTGCAAGAAAAAAACCCTGCCTTCAAGCCGGTTCTTGCAA GAATTCAAAAGAAGTTCTAAGTTTATTGCAAG_AAAAAACCCTGCCTTCAAGCCGGTTCTTGCAA GA G MTHFD1L Ensembl:ENSG00000120254 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs769597461 Functional Loss DEL TCGA 33..33 33 COAD 1 - Human_RBP_ID_2983338,Human_RBP_ID_17305228 Human_Splice_Rec_822726,Human_Splice_Rec_822727,Human_Splice_Rec_822780,Human_Splice_Rec_822781,Human_Splice_Rec_822834,Human_Splice_Rec_822835,Human_Splice_Rec_822848,Human_Splice_Rec_822849,Human_Splice_Rec_822868,Human_Splice_Rec_822869,Human_Splice_Rec_822922,Human_Splice_Rec_822923,Human_Splice_Rec_822942,Human_Splice_Rec_822943 Human_miRNA_ID_2931562 RMVar_hsa_circ_27359,RMVar_hsa_circ_295211,RMVar_hsa_circ_335989,RMVar_hsa_circ_242293,RMVar_hsa_circ_75615,RMVar_hsa_circ_339453,RMVar_hsa_circ_365241,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_296900,RMVar_hsa_circ_47344,RMVar_hsa_circ_294609,RMVar_hsa_circ_36630,RMVar_hsa_circ_242294 114068 RMVar_ID_114068 Human_SNP_ID_866012677 m1A Human chr6 - 30703964 30703964 30703964 CCCTGGCTCCCTCGCAGCTCCCATTGACCATAAGCCTTGCTCTGCACCCTTGGAACCTAAATCCC CCCTGGCTCCCTCGCAGCTCCCATTGACCATACGCCTTGCTCTGCACCCTTGGAACCTAAATCCC T G MDC1 Ensembl:ENSG00000137337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30703913..30704014 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_660963,Human_RBP_ID_1670465,Human_RBP_ID_3805884,Human_RBP_ID_4879831,Human_RBP_ID_7591494,Human_RBP_ID_8899781,Human_RBP_ID_15783969,Human_RBP_ID_17306361,Human_RBP_ID_17419527,Human_RBP_ID_18862431 114069 RMVar_ID_114069 Human_SNP_ID_866028561 m1A Human chr6 - 31729223 31729223 31729223 TGTCTCCTCCTTTTCTGTTTCTTCTCCCAGACAGGTGAAGAAACAAGAAAACTAAGAAATCCGAG TGTCTCCTCCTTTTCTGTTTCTTCTCCCAGACCGGTGAAGAAACAAGAAAACTAAGAAATCCGAG T G DDAH2 Ensembl:ENSG00000213722 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:31728995..31729289 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary Human_RBP_ID_3806350,Human_RBP_ID_21324952,Human_RBP_ID_22831329,Human_RBP_ID_25997049 Human_Splice_Rec_753788,Human_Splice_Rec_753810,Human_Splice_Rec_753820,Human_Splice_Rec_753830 114070 RMVar_ID_114070 Human_SNP_ID_866033060 m1A Human chr6 - 52283402 52283402 52283402 ATGGTGATATGTGGTGGCTGTTTTGCAGGAAGACCAGGGAATTTATCAGAGCAAAGTTCGGGAGC ATGGTGATATGTGGTGGCTGTTTTGCAGGAAGTCCAGGGAATTTATCAGAGCAAAGTTCGGGAGC T A MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr6:52283351..52283425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_2023230,Human_RBP_ID_4904092,Human_RBP_ID_7614701,Human_RBP_ID_15847106 Human_Splice_Rec_777292,Human_Splice_Rec_777354 Human_miRNA_ID_2906978,Human_miRNA_ID_3025810 RMVar_hsa_circ_78156,RMVar_hsa_circ_238907,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924,RMVar_hsa_circ_125321,RMVar_hsa_circ_238928,RMVar_hsa_circ_6182,RMVar_hsa_circ_6725,RMVar_hsa_circ_354042 114071 RMVar_ID_114071 Human_SNP_ID_866066827 m1A Human chr6 - 43229356 43229356 43229356 GTACTTCTGCGGGAGCATTCGCGGCGGACGCGAGGACAGGACGCTGTACGAGCGGATCGTGTCTC GTACTTCTGCGGGAGCATTCGCGGCGGACGCGGGGACAGGACGCTGTACGAGCGGATCGTGTCTC T C DNPH1 Ensembl:ENSG00000112667 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:43229113..43229450 26863196 MeRIP-seq:(Medium) rs1474003608 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_665089,Human_RBP_ID_842097,Human_RBP_ID_4904050,Human_RBP_ID_5327164,Human_RBP_ID_5478227,Human_RBP_ID_8944019,Human_RBP_ID_22460731,Human_RBP_ID_22514377 Human_Splice_Rec_772361,Human_Splice_Rec_772373 RMVar_hsa_circ_238595,RMVar_hsa_circ_98608 114072 RMVar_ID_114072 Human_SNP_ID_866066993 m1A Human chr6 + 31637320 31637320 31637320 AGTCTTCCGCACCCAGCGCGTCGACCTTTACCAGCAGGTGAAGGAGAAACCCTTGTGGCCCCAAC AGTCTTCCGCACCCAGCGCGTCGACCTTTACCCGCAGGTGAAGGAGAAACCCTTGTGGCCCCAAC A C PRRC2A Ensembl:ENSG00000204469 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:31637226..31637325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_1046861,Human_RBP_ID_23060396,Human_RBP_ID_26828204,Human_RBP_ID_27568364 Human_Splice_Rec_752504,Human_Splice_Rec_752505,Human_Splice_Rec_752564,Human_Splice_Rec_752565,Human_Splice_Rec_752610,Human_Splice_Rec_752614,Human_Splice_Rec_752616,Human_Splice_Rec_752617 114073 RMVar_ID_114073 Human_SNP_ID_866070132 m1A Human chr6 + 2779420 2779420 2779420 TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCAGTAGAGTTCTGATCACAGAGAATGACGTGAAG TCTGTAAGAAGAGTGGGCAATCCTATTCTCCCGGTAGAGTTCTGATCACAGAGAATGACGTGAAG A G WRNIP1 Ensembl:ENSG00000124535 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:2779251..2785350 32194978 MeRIP-seq:(Medium) rs1182152203 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 5 lung Human_RBP_ID_659868,Human_RBP_ID_2017201,Human_RBP_ID_8899400,Human_RBP_ID_9308109,Human_RBP_ID_15773178,Human_RBP_ID_18072053,Human_RBP_ID_22513842,Human_RBP_ID_23059251 Human_Splice_Rec_733311,Human_Splice_Rec_733323,Human_Splice_Rec_733335,Human_Splice_Rec_733347,Human_Splice_Rec_733357 Human_miRNA_ID_2211918,Human_miRNA_ID_2568006 RMVar_hsa_circ_13644,RMVar_hsa_circ_283108,RMVar_hsa_circ_309443,RMVar_hsa_circ_365013,RMVar_hsa_circ_236901,RMVar_hsa_circ_125205,RMVar_hsa_circ_289201,RMVar_hsa_circ_370942,RMVar_hsa_circ_277934,RMVar_hsa_circ_236902,RMVar_hsa_circ_236899,RMVar_hsa_circ_236900 114074 RMVar_ID_114074 Human_SNP_ID_866070905 m1A Human chr6 + 81751965 81751965 81751965 TGCTCCCAGTTCAGCACATTGCAGTGCGCCGTAGGGCTTTCGCAATAGTCCAAGCAATGCCCACC TGCTCCCAGTTCAGCACATTGCAGTGCGCCGTCGGGCTTTCGCAATAGTCCAAGCAATGCCCACC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:81751917..81752200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114075 RMVar_ID_114075 Human_SNP_ID_866073094 m1A Human chr6 - 132814820 132814820 132814820 TTCCGCCAGCTCTAGCCCCACGCCTCAGCCGCACCCCGACCCCAACTCCAACCCCGGCCCCTGGG TTCCGCCAGCTCTAGCCCCACGCCTCAGCCGCCCCCCGACCCCAACTCCAACCCCGGCCCCTGGG T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr6:132814814..132814972 26863196 MeRIP-seq:(Medium) rs780383422 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary 114076 RMVar_ID_114076 Human_SNP_ID_866077010 m1A Human chr6 - 26597152 26597152 26597152 CGCTGAGAAGGTTGCGGACGTGCAGGGGCCGGAAGCGCGGCGGGATATGGCCCAGGTACACAATA CGCTGAGAAGGTTGCGGACGTGCAGGGGCCGGTAGCGCGGCGGGATATGGCCCAGGTACACAATA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:26597051..26597152 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 114077 RMVar_ID_114077 Human_SNP_ID_866081291 m1A Human chr6 + 13615511 13615511 13615511 AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGAAGACGAGGAAGGGGACGATGAGTTTGACGATGA AGCAGCGGCGCGGCCGCCGAGCCCCTGGAGGACGACGAGGAAGGGGACGATGAGTTTGACGATGA A C NOL7 Ensembl:ENSG00000225921 Protein coding CDS GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576 HEK293T,H2O2 treatment chr6:13615424..13615572 26863410 MeRIP-seq:(Medium) rs545142311 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_4865061,Human_RBP_ID_9401616,Human_RBP_ID_26353405 114078 RMVar_ID_114078 Human_SNP_ID_866088109 m1A Human chr6 + 31355418 31355417 31355418 CAGAAGGCACCACCACAGCTGCCCACTTCTGGAAGGTTCTATCTCCTGCTGGTCTGGTCTCCACA CAGAAGGCACCACCACAGCTGCCCACTTCTGG_AGGTTCTATCTCCTGCTGGTCTGGTCTCCACA GA G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31355101..31355675 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - 114079 RMVar_ID_114079 Human_SNP_ID_866093822 m1A Human chr6 + 111720057 111720057 111720057 TTTATCCTTACATTGCACACAGCCCATTATCTAAATTCCTGCCAAAGACAAAAAAGGGGGCACGT TTTATCCTTACATTGCACACAGCCCATTATCTGAATTCCTGCCAAAGACAAAAAAGGGGGCACGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:111719965..111720102 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 8 stomach 114080 RMVar_ID_114080 Human_SNP_ID_866119956 m1A Human chr6 - 2841724 2841724 2841724 TCCCTCGCTCAGCTTCCAGCCCGGCACCCCCCACCCCCCAGGCTCAGGCCCCTCAGACCCGCAGC TCCCTCGCTCAGCTTCCAGCCCGGCACCCCCCCCCCCCCAGGCTCAGGCCCCTCAGACCCGCAGC T G SERPINB1 Ensembl:ENSG00000021355 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:2841717..2841809 26863196 MeRIP-seq:(Medium) rs887518736 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_113888,RMVar_hsa_circ_236906,RMVar_hsa_circ_81654,RMVar_hsa_circ_90541,RMVar_hsa_circ_114731,RMVar_hsa_circ_236908,RMVar_hsa_circ_236909,RMVar_hsa_circ_236910 114081 RMVar_ID_114081 Human_SNP_ID_866120458 m1A Human chr6 + 165749459 165749456 165749460 ACCACCATCACCATCACCACCATCACATCACCATCATCAACAACACCATCAACACCATCATCACC ACCACCATCACCATCACCACCATCACATCA____CATCAACAACACCATCAACACCATCATCACC ACCAT A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:165749184..165749493 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 SKCA 1 - 114082 RMVar_ID_114082 Human_SNP_ID_866134935 m1A Human chr6 + 33398334 33398334 33398334 CCTGGGTGCAACGACCAAAATTACCACATCCCACCCAAGAGTTCCATCCCTCACTACAGTGCCAC CCTGGGTGCAACGACCAAAATTACCACATCCCGCCCAAGAGTTCCATCCCTCACTACAGTGCCAC A G KIFC1 Ensembl:ENSG00000237649 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:33398165..33398387 32194978 MeRIP-seq:(Medium) rs1329903242 Functional Loss SNV COSMIC 33..33 33 face squamous_cell_carcinoma,skin squamous_cell_carcinoma 1 skin,head and neck Human_RBP_ID_1047132,Human_RBP_ID_5152134,Human_RBP_ID_5478114,Human_RBP_ID_8643055,Human_RBP_ID_17306769,Human_RBP_ID_17419809,Human_RBP_ID_17710624,Human_RBP_ID_18074457 Human_Splice_Rec_761714,Human_Splice_Rec_761715,Human_Splice_Rec_761734,Human_Splice_Rec_761735 RMVar_hsa_circ_107733,RMVar_hsa_circ_305629,RMVar_hsa_circ_237859 114083 RMVar_ID_114083 Human_SNP_ID_866155957 m1A Human chr6 + 36596837 36596837 36596837 GGCAATCTTGGAAACAATGGCAACAAGACGGAATTGGAACGGGCTTTTGGCTACTATGGACCACT GGCAATCTTGGAAACAATGGCAACAAGACGGAGTTGGAACGGGCTTTTGGCTACTATGGACCACT A G SRSF3 Ensembl:ENSG00000112081 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:36594711..36597017;chr6:36596751..36597003;chr6:36596751..36597028 26863196 MeRIP-seq:(Medium) rs1179651719 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_663637,Human_RBP_ID_1672671,Human_RBP_ID_2020371,Human_RBP_ID_3808265,Human_RBP_ID_4913328,Human_RBP_ID_5219188,Human_RBP_ID_5617909,Human_RBP_ID_7600811,Human_RBP_ID_8644305,Human_RBP_ID_8901201,Human_RBP_ID_9400496,Human_RBP_ID_15811831,Human_RBP_ID_17536049,Human_RBP_ID_18075562,Human_RBP_ID_18864902,Human_RBP_ID_22772743,Human_RBP_ID_24160836,Human_RBP_ID_26353187 Human_Splice_Rec_766020,Human_Splice_Rec_766026,Human_Splice_Rec_766036,Human_Splice_Rec_766038,Human_Splice_Rec_766044,Human_Splice_Rec_766056 Human_miRNA_ID_2667848 RMVar_hsa_circ_99475,RMVar_hsa_circ_94942,RMVar_hsa_circ_238149,RMVar_hsa_circ_238150 114084 RMVar_ID_114084 Human_SNP_ID_866157229 m1A Human chr6 - 30341974 30341974 30341974 TTCCATAGCCGCACCCGCCAGTAGCCAGTCTCAGGGAGTGGAGTCAACTCGCCCTTTCGGCTCAC TTCCATAGCCGCACCCGCCAGTAGCCAGTCTCGGGGAGTGGAGTCAACTCGCCCTTTCGGCTCAC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:30341839..30341989 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 114085 RMVar_ID_114085 Human_SNP_ID_866159494 m1A Human chr6 + 42889285 42889285 42889285 CAACATGGAGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTG CAACATGGAGAAATTCTGTCCCTACTGAAAATGCAAAATTAGCCGGATGTGGTGGTGCATGCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1134326 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26540170 114086 RMVar_ID_114086 Human_SNP_ID_866164939 m1A Human chr6 + 26124438 26124438 26124438 CCTGACCGCCGAGATCCTGGAGCTGGCCGGCAACGCGGCTCGCGACAACAAGAAGACTCGCATCA CCTGACCGCCGAGATCCTGGAGCTGGCCGGCATCGCGGCTCGCGACAACAAGAAGACTCGCATCA A T H2AC6 Ensembl:ENSG00000180573 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:26124389..26124635 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_251703,Human_RBP_ID_841603,Human_RBP_ID_951573,Human_RBP_ID_1046012,Human_RBP_ID_1668856,Human_RBP_ID_2016697,Human_RBP_ID_3804180,Human_RBP_ID_4904553,Human_RBP_ID_5477764,Human_RBP_ID_8640017,Human_RBP_ID_9192833,Human_RBP_ID_15770072,Human_RBP_ID_22104689,Human_RBP_ID_22460447,Human_RBP_ID_22534141,Human_RBP_ID_26534393,Human_RBP_ID_27093662,Human_RBP_ID_27343967,Human_RBP_ID_27521885 RMVar_hsa_circ_93847,RMVar_hsa_circ_237738 114087 RMVar_ID_114087 Human_SNP_ID_866165842 m1A Human chr6 + 43625546 43625546 43625546 TTCCCAGAGTCCACATTCCCCAGGACGGCCACACGGAGGTCTAGGAACTGTGGATGAATTGCCAG TTCCCAGAGTCCACATTCCCCAGGACGGCCACGCGGAGGTCTAGGAACTGTGGATGAATTGCCAG A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43625498..43626403 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 114088 RMVar_ID_114088 Human_SNP_ID_866194757 m1A Human chr6 + 170553239 170553239 170553239 GCCAGGAGCCGAATACATGGCTGTAGAGGACAACATCGCACGGCTGCGCCTGCGGATCCGACACT GCCAGGAGCCGAATACATGGCTGTAGAGGACAGCATCGCACGGCTGCGCCTGCGGATCCGACACT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:170553189..170553300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - 114089 RMVar_ID_114089 Human_SNP_ID_866228891 m1A Human chr6 - 110101994 110101994 110101994 GCTTTGCAAGCTCCAGCAGTACCACCACCTCCAGCTCCTCTTCAGATTGCCCCTGGAGTTCTTCA GCTTTGCAAGCTCCAGCAGTACCACCACCTCCCGCTCCTCTTCAGATTGCCCCTGGAGTTCTTCA T G WASF1 Ensembl:ENSG00000112290 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:110101945..110102161 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5134200,Human_RBP_ID_9185522,Human_RBP_ID_17310357,Human_RBP_ID_18958583,Human_RBP_ID_24128476 Human_miRNA_ID_1386578 RMVar_hsa_circ_39421 114090 RMVar_ID_114090 Human_SNP_ID_866240504 m1A Human chr6 + 38703005 38703005 38703005 TGGTACTGGGGTCCGCGTCGGAGCAGCAACTGAGGGCGGCCTCGTCCGTGAGGCCGCCGGACGGG TGGTACTGGGGTCCGCGTCGGAGCAGCAACTGGGGGCGGCCTCGTCCGTGAGGCCGCCGGACGGG A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:38702951..38703150 26863196 MeRIP-seq:(Medium) rs751878828 Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 114091 RMVar_ID_114091 Human_SNP_ID_866244792 m1A Human chr6 + 20730378 20730378 20730378 GAAAAGAAAGAAAGATAGATAGATGGAGCCCGACCCGAAAAAAAAGGAAGAAAGGAAGAAAGAGA GAAAAGAAAGAAAGATAGATAGATGGAGCCCGTCCCGAAAAAAAAGGAAGAAAGGAAGAAAGAGA A T CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:20730274..20730546 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_363102,RMVar_hsa_circ_314276,RMVar_hsa_circ_330336,RMVar_hsa_circ_361834,RMVar_hsa_circ_315011,RMVar_hsa_circ_36305,RMVar_hsa_circ_237513 114092 RMVar_ID_114092 Human_SNP_ID_866253942 m1A Human chr6 - 27838598 27838584 27838599 AAAAAACAGGAAGACGGTAGCTCTGTCAACCTACCGCTTATTCACTGCTTCTTAACGCAAGTGGG AAAAAACAGGAAGACGGTAGCTCTGTCAACC_______________GCTTCTTAACGCAAGTGGG CAGTGAATAAGCGGTA C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:27838576..27838600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..46 33 BLCA 1 - 114093 RMVar_ID_114093 Human_SNP_ID_866323239 m1A Human chr6 + 7582883 7582883 7582883 CCTGAATCAGTGGAAGACTCAATATTCCCGCAAGGAGGAGGCTATTAGGAAGATAGAATCGGAAA CCTGAATCAGTGGAAGACTCAATATTCCCGCACGGAGGAGGCTATTAGGAAGATAGAATCGGAAA A C DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:7582751..7582950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_8903374,Human_RBP_ID_18080552,Human_RBP_ID_22773238 114094 RMVar_ID_114094 Human_SNP_ID_866345574 m1A Human chr6 + 27838698 27838698 27838698 CCGAGCCCTCAAAGTCCGCTCCTGCCCCGAAGAAAGGCTCCAAGAAGGCAGTGACAAAGGCCCAG CCGAGCCCTCAAAGTCCGCTCCTGCCCCGAAGCAAGGCTCCAAGAAGGCAGTGACAAAGGCCCAG A C H2BC15 Ensembl:ENSG00000233822 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:27838587..27838801 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate Human_RBP_ID_4877442,Human_RBP_ID_9193064,Human_RBP_ID_9336019,Human_RBP_ID_9400131,Human_RBP_ID_22462525,Human_RBP_ID_22706160,Human_RBP_ID_24548549,Human_RBP_ID_26353133,Human_RBP_ID_26828077,Human_RBP_ID_27094329 114095 RMVar_ID_114095 Human_SNP_ID_866361227 m1A Human chr6 + 7579748 7579748 7579748 GTTCTACTGCAGGAAGAAGGCACCCGGAAGAGAGAATATGAAAATGAGCTGGCAAAGGTAAGAAA GTTCTACTGCAGGAAGAAGGCACCCGGAAGAGTGAATATGAAAATGAGCTGGCAAAGGTAAGAAA A T DSP Ensembl:ENSG00000096696 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:7579499..7579836 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_3017580,Human_RBP_ID_7627561,Human_RBP_ID_8903334,Human_RBP_ID_9399929,Human_RBP_ID_27525948 Human_Splice_Rec_736097 114096 RMVar_ID_114096 Human_SNP_ID_866368651 m1A Human chr6 + 160992027 160992027 160992027 ATGGAGGAGCCGCCGCCACCGCCGCCGCCGCCACCACCGCCACCGGAACCCGAGACCGAGTCAGA ATGGAGGAGCCGCCGCCACCGCCGCCGCCGCCGCCACCGCCACCGGAACCCGAGACCGAGTCAGA A G MAP3K4 Ensembl:ENSG00000085511 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:160991859..160992033 26863196 MeRIP-seq:(Medium) rs1562464630 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_830447,Human_Splice_Rec_830497,Human_Splice_Rec_830501,Human_Splice_Rec_830553,Human_Splice_Rec_830605,Human_Splice_Rec_830655,Human_Splice_Rec_830709 114097 RMVar_ID_114097 Human_SNP_ID_866374029 m1A Human chr6 + 43158949 43158949 43158949 AGAGACAAGTGAAGGTGTCTGCCCTGGGCCTCAGCAAGGATGTGTACAACAGGTAGAAGGGCATG AGAGACAAGTGAAGGTGTCTGCCCTGGGCCTCGGCAAGGATGTGTACAACAGGTAGAAGGGCATG A G PTK7 Ensembl:ENSG00000112655 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43158899..43161300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 10 large intestine Human_RBP_ID_664993,Human_RBP_ID_2021644,Human_RBP_ID_5532447,Human_RBP_ID_7608473,Human_RBP_ID_9402113,Human_RBP_ID_17663763 Human_Splice_Rec_771689,Human_Splice_Rec_771725,Human_Splice_Rec_771769,Human_Splice_Rec_771803,Human_Splice_Rec_771839,Human_Splice_Rec_771875,Human_Splice_Rec_771911,Human_Splice_Rec_771949,Human_Splice_Rec_771973,Human_Splice_Rec_772011,Human_Splice_Rec_772017 Human_miRNA_ID_1038327,Human_miRNA_ID_1474357,Human_miRNA_ID_2477386,Human_miRNA_ID_2489991,Human_miRNA_ID_2752077 RMVar_hsa_circ_238561,RMVar_hsa_circ_88836,RMVar_hsa_circ_84927,RMVar_hsa_circ_238560,RMVar_hsa_circ_96329,RMVar_hsa_circ_238564,RMVar_hsa_circ_119771,RMVar_hsa_circ_238565,RMVar_hsa_circ_49659,RMVar_hsa_circ_19058,RMVar_hsa_circ_110599,RMVar_hsa_circ_238567,RMVar_hsa_circ_78053,RMVar_hsa_circ_79476,RMVar_hsa_circ_238571,RMVar_hsa_circ_302394,RMVar_hsa_circ_238572 114098 RMVar_ID_114098 Human_SNP_ID_866380307 m1A Human chr6 + 43779985 43779985 43779985 GCTCGGAAGAGTGTCTGGTGAGATGGTGTAGCAGGCTTTGACAGGCTGGGGAGAGAACTCCCTGC GCTCGGAAGAGTGTCTGGTGAGATGGTGTAGCTGGCTTTGACAGGCTGGGGAGAGAACTCCCTGC A T VEGFA Ensembl:ENSG00000112715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43779982..43780113 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 25 ovary RMVar_hsa_circ_74333,RMVar_hsa_circ_350327 114099 RMVar_ID_114099 Human_SNP_ID_866388692 m1A Human chr6 - 52267880 52267880 52267880 AGATGAAGAGGAGAAAAGCCAAGAGGACCAGGAGCAGAAGAGGAAGAGGTAAGGTGGGGCAAGCA AGATGAAGAGGAGAAAAGCCAAGAGGACCAGGGGCAGAAGAGGAAGAGGTAAGGTGGGGCAAGCA T C MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:52266038..52268014 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV,LAML 2 - Human_RBP_ID_251241,Human_RBP_ID_841533,Human_RBP_ID_949767,Human_RBP_ID_3010508,Human_RBP_ID_5618012,Human_RBP_ID_9400725,Human_RBP_ID_10288732,Human_RBP_ID_18539164,Human_RBP_ID_22534212,Human_RBP_ID_22746370,Human_RBP_ID_23067593,Human_RBP_ID_23120287,Human_RBP_ID_24166289,Human_RBP_ID_24387119,Human_RBP_ID_24548420,Human_RBP_ID_24554643,Human_RBP_ID_26354128,Human_RBP_ID_27827772 Human_Splice_Rec_777316,Human_Splice_Rec_777317,Human_Splice_Rec_777346,Human_Splice_Rec_777347,Human_Splice_Rec_777378,Human_Splice_Rec_777379,Human_Splice_Rec_777408,Human_Splice_Rec_777409,Human_Splice_Rec_777422,Human_Splice_Rec_777423 RMVar_hsa_circ_5805,RMVar_hsa_circ_238913,RMVar_hsa_circ_83669,RMVar_hsa_circ_121340,RMVar_hsa_circ_121805,RMVar_hsa_circ_113495,RMVar_hsa_circ_89985,RMVar_hsa_circ_99124,RMVar_hsa_circ_89607,RMVar_hsa_circ_79221,RMVar_hsa_circ_79823,RMVar_hsa_circ_238915,RMVar_hsa_circ_78156,RMVar_hsa_circ_238916,RMVar_hsa_circ_238914,RMVar_hsa_circ_238909,RMVar_hsa_circ_238911,RMVar_hsa_circ_238912,RMVar_hsa_circ_238910,RMVar_hsa_circ_238907,RMVar_hsa_circ_238908,RMVar_hsa_circ_335585,RMVar_hsa_circ_110326,RMVar_hsa_circ_110458,RMVar_hsa_circ_6089,RMVar_hsa_circ_115005,RMVar_hsa_circ_238919,RMVar_hsa_circ_238920,RMVar_hsa_circ_108765,RMVar_hsa_circ_238921,RMVar_hsa_circ_238922,RMVar_hsa_circ_238923,RMVar_hsa_circ_280485,RMVar_hsa_circ_339495,RMVar_hsa_circ_353656,RMVar_hsa_circ_281477,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924,RMVar_hsa_circ_238926,RMVar_hsa_circ_238927,RMVar_hsa_circ_238925 114100 RMVar_ID_114100 Human_SNP_ID_866396861 m1A Human chr6 + 156901464 156901464 156901464 GCCATATTACAGCCAGCAGCCGCAGCCCCCGCACCTCCCACCCCAGGCGCAGTATCTGCCGTCCC GCCATATTACAGCCAGCAGCCGCAGCCCCCGCGCCTCCCACCCCAGGCGCAGTATCTGCCGTCCC A G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr6:156901414..156901515 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_251110,Human_RBP_ID_5532910,Human_RBP_ID_17422175,Human_RBP_ID_26355660 Human_Splice_Rec_826969,Human_Splice_Rec_827004,Human_Splice_Rec_827005,Human_Splice_Rec_827042,Human_Splice_Rec_827043,Human_Splice_Rec_827079,Human_Splice_Rec_827114,Human_Splice_Rec_827115,Human_Splice_Rec_827124,Human_Splice_Rec_827125,Human_Splice_Rec_827148,Human_Splice_Rec_827149,Human_Splice_Rec_827158,Human_Splice_Rec_827159,Human_Splice_Rec_827194,Human_Splice_Rec_827195,Human_Splice_Rec_827200,Human_Splice_Rec_827202,Human_Splice_Rec_827203,Human_Splice_Rec_827207 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_106096,RMVar_hsa_circ_242550,RMVar_hsa_circ_344061,RMVar_hsa_circ_276425,RMVar_hsa_circ_242565,RMVar_hsa_circ_242566,RMVar_hsa_circ_242567 114101 RMVar_ID_114101 Human_SNP_ID_866432276 m1A Human chr6 - 30490412 30490412 30490412 TAGGCTCTCTGGTGCTCCGCCTCAGAGGCATCATTTGACTTTTGCTCGGAGATCTGAGCCGCCGT TAGGCTCTCTGGTGCTCCGCCTCAGAGGCATCGTTTGACTTTTGCTCGGAGATCTGAGCCGCCGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:30490363..30490446 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 114102 RMVar_ID_114102 Human_SNP_ID_866438961 m1A Human chr6 - 52284718 52284718 52284718 AAGTTTTCGCGCCGGGGTGGAGTCATCCTGGGAACCTCCACGCGACTTTGGTGGAGGTAGTTCTT AAGTTTTCGCGCCGGGGTGGAGTCATCCTGGGCACCTCCACGCGACTTTGGTGGAGGTAGTTCTT T G MCM3 Ensembl:ENSG00000112118 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:52284518..52284775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_1327978,Human_RBP_ID_4893541,Human_RBP_ID_8905848,Human_RBP_ID_9336708 RMVar_hsa_circ_78156,RMVar_hsa_circ_238907,RMVar_hsa_circ_116391,RMVar_hsa_circ_238924 114103 RMVar_ID_114103 Human_SNP_ID_866440477 m1A Human chr6 + 37171304 37171304 37171304 TTCGACTTCATCACGGAAAGGGGAGCCCTGCAAGAGGAGCTGGCCCGCAGCTTCTTCTGGCAGGT TTCGACTTCATCACGGAAAGGGGAGCCCTGCACGAGGAGCTGGCCCGCAGCTTCTTCTGGCAGGT A C PIM1 Ensembl:ENSG00000137193 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:37171254..37171418 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_790366,Human_RBP_ID_841411,Human_RBP_ID_9402063,Human_RBP_ID_17421678,Human_RBP_ID_18865071,Human_RBP_ID_22106428,Human_RBP_ID_22534106,Human_RBP_ID_22616397,Human_RBP_ID_27346917 RMVar_hsa_circ_87286,RMVar_hsa_circ_98763,RMVar_hsa_circ_104996,RMVar_hsa_circ_238175,RMVar_hsa_circ_238176,RMVar_hsa_circ_238177 114104 RMVar_ID_114104 Human_SNP_ID_866464218 m1A Human chr6 - 31663943 31663943 31663943 CTGGGTGGGGGTCTGTGAGCTGAGTGGCAGGGATGCGGCTCAGCTCGCTGAAGAAGCTGGCTTCC CTGGGTGGGGGTCTGTGAGCTGAGTGGCAGGGGTGCGGCTCAGCTCGCTGAAGAAGCTGGCTTCC T C GPANK1 Ensembl:ENSG00000204438 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:31663895..31663975 26863196 MeRIP-seq:(Medium) rs201945052 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,central_nervous_system astrocytoma_Grade_IV,colon adenocarcinoma,brain astrocytoma_Grade_IV,large_intestine adenocarcinoma 11 large intestine,brain Human_RBP_ID_251891,Human_RBP_ID_791340,Human_RBP_ID_949253,Human_RBP_ID_5327096,Human_RBP_ID_5399395,Human_RBP_ID_5478523,Human_RBP_ID_19016642,Human_RBP_ID_22104870,Human_RBP_ID_22728142,Human_RBP_ID_26353648,Human_RBP_ID_26792942 Human_Splice_Rec_753115,Human_Splice_Rec_753121,Human_Splice_Rec_753127,Human_Splice_Rec_753133,Human_Splice_Rec_753139 114105 RMVar_ID_114105 Human_SNP_ID_866472890 m1A Human chr6 + 165987925 165987925 165987925 GTCCATCTCAGCTCAAGCTCCCAGCAGCAGCAACTTCGGACTCAGACCTCTCTCTTTAGAACATG GTCCATCTCAGCTCAAGCTCCCAGCAGCAGCACCTTCGGACTCAGACCTCTCTCTTTAGAACATG A C LINC00602 Ensembl:ENSG00000281832 lincRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:165987876..165987925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114106 RMVar_ID_114106 Human_SNP_ID_866477758 m1A Human chr6 - 136389424 136389424 136389424 CCTGGAAGAGCGGAAGAAGAGGTTGGAGGAGCAGAGGCAGAAGGAGGAGCGGAGGAGGGCTGCTG CCTGGAAGAGCGGAAGAAGAGGTTGGAGGAGCTGAGGCAGAAGGAGGAGCGGAGGAGGGCTGCTG T A MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:136389376..136389425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_80392 Human_Splice_Rec_816318,Human_Splice_Rec_816319,Human_Splice_Rec_816352,Human_Splice_Rec_816353,Human_Splice_Rec_816416,Human_Splice_Rec_816417,Human_Splice_Rec_816448,Human_Splice_Rec_816449,Human_Splice_Rec_816484,Human_Splice_Rec_816485,Human_Splice_Rec_816518,Human_Splice_Rec_816519,Human_Splice_Rec_816552,Human_Splice_Rec_816553 RMVar_hsa_circ_24411,RMVar_hsa_circ_59035,RMVar_hsa_circ_265139,RMVar_hsa_circ_266867,RMVar_hsa_circ_296571,RMVar_hsa_circ_297131,RMVar_hsa_circ_241705,RMVar_hsa_circ_241703,RMVar_hsa_circ_241702,RMVar_hsa_circ_285301,RMVar_hsa_circ_241706,RMVar_hsa_circ_296001 114107 RMVar_ID_114107 Human_SNP_ID_866495926 m1A Human chr6 - 33211897 33211897 33211897 GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCACCCCCACCCTCCCCGCCACACCCATCAGGTCC GCAGGCTCCTCAGGACCGTCACCTCCTCCGGCCCCCCCACCCTCCCCGCCACACCCATCAGGTCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:33211851..33212000 26863196 MeRIP-seq:(Medium) rs754640364 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 1 head and neck 114108 RMVar_ID_114108 Human_SNP_ID_866506483 m1A Human chr6 - 41937291 41937291 41937291 CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGACCGACAGGCCTTGGTCAAAAAGCATGCCCAGA CTTCATTCTGCACCGGCTCTCTCTGCCCCGTGCCCGACAGGCCTTGGTCAAAAAGCATGCCCAGA T G CCND3 Ensembl:ENSG00000112576 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:41937190..41937291 32194978 MeRIP-seq:(Medium) rs147099303 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 8 head and neck Human_RBP_ID_789889,Human_RBP_ID_8901476,Human_RBP_ID_9309300,Human_RBP_ID_17710827,Human_RBP_ID_18195590 Human_Splice_Rec_769753,Human_Splice_Rec_769759,Human_Splice_Rec_769767,Human_Splice_Rec_769775,Human_Splice_Rec_769781,Human_Splice_Rec_769789,Human_Splice_Rec_769795,Human_Splice_Rec_769803,Human_Splice_Rec_769807,Human_Splice_Rec_769811,Human_Splice_Rec_769815,Human_Splice_Rec_769819,Human_Splice_Rec_769825,Human_Splice_Rec_769829 Human_miRNA_ID_2225068 RMVar_hsa_circ_92809,RMVar_hsa_circ_75750,RMVar_hsa_circ_238337,RMVar_hsa_circ_238339,RMVar_hsa_circ_238338,RMVar_hsa_circ_372050 114109 RMVar_ID_114109 Human_SNP_ID_866512491 m1A Human chr6 + 31669903 31669903 31669903 AGCTGCAGCTCCAAGCCGCCAGCAACTTCAAGAGCCCAGTCAAGACGATTCGCTGATTCCCTCCC AGCTGCAGCTCCAAGCCGCCAGCAACTTCAAGTGCCCAGTCAAGACGATTCGCTGATTCCCTCCC A T CSNK2B,AL662899.4 Ensembl:ENSG00000204435,Ensembl:ENSG00000263020 Protein coding,Protein coding CDS,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31669833..31669971 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 14 liver Human_RBP_ID_252567,Human_RBP_ID_661630,Human_RBP_ID_1671085,Human_RBP_ID_8642282,Human_RBP_ID_18958147,Human_RBP_ID_23068996,Human_RBP_ID_27096175 Human_Splice_Rec_753164,Human_Splice_Rec_753176,Human_Splice_Rec_753184,Human_Splice_Rec_753210,Human_Splice_Rec_753222 RMVar_hsa_circ_17362 114110 RMVar_ID_114110 Human_SNP_ID_866516796 m1A Human chr6 + 31795240 31795240 31795240 GGGTGGACATAGTTATGAGAAGGTCCGAACGAAGTGGAAAAACCTAAGGAGAAAGAGAGACAGGG GGGTGGACATAGTTATGAGAAGGTCCGAACGACGTGGAAAAACCTAAGGAGAAAGAGAGACAGGG A C RF00017-4498,RF00017-4498:2,RF00017-4501 RNACentral:URS0000930330,RNACentral:URS0000923951,RNACentral:URS0000972B66 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:31795226..31795300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 114111 RMVar_ID_114111 Human_SNP_ID_866531254 m1A Human chr6 + 170400105 170400105 170400105 GAACTATGTCATAAGCCTTAGGAGTGAGTGAGAAAGGTAGAACTATGTCATAACCCTTAGGAGTG GAACTATGTCATAAGCCTTAGGAGTGAGTGAGGAAGGTAGAACTATGTCATAACCCTTAGGAGTG A G FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr6:170400085..170400169 26863410 MeRIP-seq:(Medium) rs1287975274 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_13315,Human_RBP_ID_1111235,Human_RBP_ID_5152268,Human_RBP_ID_5242751,Human_RBP_ID_5400073,Human_RBP_ID_5478639,Human_RBP_ID_15744867,Human_RBP_ID_21948483,Human_RBP_ID_23259203,Human_RBP_ID_24149646,Human_RBP_ID_24386960 RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_91561,RMVar_hsa_circ_243154,RMVar_hsa_circ_332497,RMVar_hsa_circ_45303,RMVar_hsa_circ_243156 114112 RMVar_ID_114112 Human_SNP_ID_866561443 m1A Human chr6 + 637860 637860 637860 TGGAGCAAACTGGTGATCCTGTTAGAGAAGTAATCTGTTAAAAGAGAAAGAAAAAAGGATTAGTA TGGAGCAAACTGGTGATCCTGTTAGAGAAGTAGTCTGTTAAAAGAGAAAGAAAAAAGGATTAGTA A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:637821..637910 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114113 RMVar_ID_114113 Human_SNP_ID_866570895 m1A Human chr6 + 43063048 43063048 43063048 CGGGATGAGCTGGCTGGCACCCAGCAGCGGCTACAGCGCAGTGAACAGGCTGTGGCTCAGCTGGA CGGGATGAGCTGGCTGGCACCCAGCAGCGGCTGCAGCGCAGTGAACAGGCTGTGGCTCAGCTGGA A G KLC4 Ensembl:ENSG00000137171 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:43062999..43063179 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_3969103,Human_RBP_ID_19017037,Human_RBP_ID_23116511,Human_RBP_ID_23120367 Human_Splice_Rec_771353,Human_Splice_Rec_771409,Human_Splice_Rec_771437,Human_Splice_Rec_771444,Human_Splice_Rec_771445,Human_Splice_Rec_771455,Human_Splice_Rec_771465,Human_Splice_Rec_771497,Human_Splice_Rec_771529,Human_Splice_Rec_771539,Human_Splice_Rec_771567 RMVar_hsa_circ_5986 114114 RMVar_ID_114114 Human_SNP_ID_866608352 m1A Human chr6 + 156778973 156778973 156778973 GCTGTGGCGGCGGCGGCCGCGGCGGCGGCGGCAGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG GCTGTGGCGGCGGCGGCCGCGGCGGCGGCGGCCGCAGCAGGAGGCGGCGGCGGCGGCGGCTATGG A C ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:156778708..156779471;chr6:156778725..156779449 26863196 MeRIP-seq:(Medium) rs1331367859 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_251105,Human_RBP_ID_5532901 Human_miRNA_ID_2511415,Human_miRNA_ID_3054238 RMVar_hsa_circ_87108,RMVar_hsa_circ_242547 114115 RMVar_ID_114115 Human_SNP_ID_866624576 m1A Human chr6 + 5368701 5368701 5368701 ATCGAGGCCTCCTGCAGCAGAGTGTGCCACCCAAAGAGCTCCAGGCAGTGTGGTGGAGCTGCTGG ATCGAGGCCTCCTGCAGCAGAGTGTGCCACCCGAAGAGCTCCAGGCAGTGTGGTGGAGCTGCTGG A G FARS2 Ensembl:ENSG00000145982 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:5368651..5404550 32194978 MeRIP-seq:(Medium) rs1453046888 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_237001,RMVar_hsa_circ_286335,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997,RMVar_hsa_circ_303679,RMVar_hsa_circ_337412,RMVar_hsa_circ_301841,RMVar_hsa_circ_237003,RMVar_hsa_circ_278872,RMVar_hsa_circ_237002,RMVar_hsa_circ_236999,RMVar_hsa_circ_237000,RMVar_hsa_circ_236998 114116 RMVar_ID_114116 Human_SNP_ID_866643689 m1A Human chr6 - 167965901 167965901 167965901 AGGCGGGGGAGGAGGGGCGCCGGGCGCGGGGGACGGGGACGGGGGCTCGTAGTCCCGGGGAAGCG AGGCGGGGGAGGAGGGGCGCCGGGCGCGGGGGGCGGGGACGGGGGCTCGTAGTCCCGGGGAAGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:167965776..167966025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114117 RMVar_ID_114117 Human_SNP_ID_866646876 m1A Human chr6 - 20128232 20128232 20128232 GGAGAGGTGAGTATAGCTGAGTTAAATACAGGAGGAGGGCTACAGGTGGCTTTGCCAGTGTTGAT GGAGAGGTGAGTATAGCTGAGTTAAATACAGGGGGAGGGCTACAGGTGGCTTTGCCAGTGTTGAT T C MBOAT1 Ensembl:ENSG00000172197 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:20128092..20128256 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_7580189 RMVar_hsa_circ_43417,RMVar_hsa_circ_43769,RMVar_hsa_circ_1027,RMVar_hsa_circ_293212,RMVar_hsa_circ_288118,RMVar_hsa_circ_237500,RMVar_hsa_circ_7000,RMVar_hsa_circ_307429,RMVar_hsa_circ_273027,RMVar_hsa_circ_237502 114118 RMVar_ID_114118 Human_SNP_ID_866694490 m1A Human chr6 + 33446656 33446656 33446656 TGTCCAACCGGAAGCTGGAAGAGTATGAGCGGAGGCTGCTGTCCCAGGAAGAACAAACCAGCAAA TGTCCAACCGGAAGCTGGAAGAGTATGAGCGGTGGCTGCTGTCCCAGGAAGAACAAACCAGCAAA A T SYNGAP1 Ensembl:ENSG00000197283 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:33446546..33446783 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 9 breast Human_RBP_ID_3968974,Human_RBP_ID_19018384,Human_RBP_ID_26353824,Human_RBP_ID_27827558 Human_Splice_Rec_762090,Human_Splice_Rec_762144,Human_Splice_Rec_762180,Human_Splice_Rec_762212,Human_Splice_Rec_762246,Human_Splice_Rec_762282,Human_Splice_Rec_762316,Human_Splice_Rec_762374,Human_Splice_Rec_762406 RMVar_hsa_circ_269040 114119 RMVar_ID_114119 Human_SNP_ID_866730703 m1A Human chr6 - 31356959 31356959 31356959 GGTCGGGCGGGTCTCAGCCCCTCCTCACCCCCAGGCTCCCACTCCATGAGGTATTTCTACACCTC GGTCGGGCGGGTCTCAGCCCCTCCTCACCCCCCGGCTCCCACTCCATGAGGTATTTCTACACCTC T G HLA-B Ensembl:ENSG00000234745 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31356876..31356975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - Human_RBP_ID_4904643 Human_miRNA_ID_96818 114120 RMVar_ID_114120 Human_SNP_ID_866743313 m1A Human chr6 - 29942781 29942781 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTGTAGAAATACCTCATGGAGTGGGAGCCTGGGGGC T A AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs2075684 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_I,head_neck squamous_cell_carcinoma,spinal_cord astrocytoma_Grade_I 30 head and neck,spinal cord,brain 114121 RMVar_ID_114121 Human_SNP_ID_866743314 m1A Human chr6 - 29942781 29942781 29942781 GCTCCCCGCGGCCGGGCCGGGACACGGATGTGAAGAAATACCTCATGGAGTGGGAGCCTGGGGGC GCTCCCCGCGGCCGGGCCGGGACACGGATGTGGAGAAATACCTCATGGAGTGGGAGCCTGGGGGC T C AL671277.1 Ensembl:ENSG00000227766 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:29942526..29943071 26863410 MeRIP-seq:(Medium) rs2075684 Functional Loss SNV TCGA,COSMIC 33..33 33 PAAD,caecum adenocarcinoma,haematopoietic_and_lymphoid_tissue plasma_cell_myeloma,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,large_intestine adenocarcinoma 31 caecum,large intestine,haematopoietic and lymphoid tissue 114122 RMVar_ID_114122 Human_SNP_ID_866765229 m1A Human chr6 + 34762700 34762700 34762700 TGGAAGAGCAGGCTCAGAGCCTGATTGACAAAACAAGTATGTTTCAATCTCTTGTTCTGCTGTGG TGGAAGAGCAGGCTCAGAGCCTGATTGACAAAGCAAGTATGTTTCAATCTCTTGTTCTGCTGTGG A G SNRPC Ensembl:ENSG00000124562 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr6:34762651..34762725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_663085,Human_RBP_ID_9350479 Human_Splice_Rec_763619,Human_Splice_Rec_763627,Human_Splice_Rec_763635,Human_Splice_Rec_763643 RMVar_hsa_circ_47598,RMVar_hsa_circ_237968,RMVar_hsa_circ_85729,RMVar_hsa_circ_342383 114123 RMVar_ID_114123 Human_SNP_ID_866780760 m1A Human chr6 + 156901471 156901471 156901471 TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCACCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA TACAGCCAGCAGCCGCAGCCCCCGCACCTCCCGCCCCAGGCGCAGTATCTGCCGTCCCAGTCCCA A G ARID1B Ensembl:ENSG00000049618 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated chr6:156901422..156901557;chr6:156901345..156901554 26863196 MeRIP-seq:(Medium) rs756099753 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_251110,Human_RBP_ID_3970521,Human_RBP_ID_5532910,Human_RBP_ID_17422175,Human_RBP_ID_26355660 Human_Splice_Rec_826969,Human_Splice_Rec_827004,Human_Splice_Rec_827005,Human_Splice_Rec_827042,Human_Splice_Rec_827043,Human_Splice_Rec_827079,Human_Splice_Rec_827114,Human_Splice_Rec_827115,Human_Splice_Rec_827124,Human_Splice_Rec_827125,Human_Splice_Rec_827148,Human_Splice_Rec_827149,Human_Splice_Rec_827158,Human_Splice_Rec_827159,Human_Splice_Rec_827194,Human_Splice_Rec_827195,Human_Splice_Rec_827200,Human_Splice_Rec_827202,Human_Splice_Rec_827203,Human_Splice_Rec_827207 RMVar_hsa_circ_79458,RMVar_hsa_circ_87108,RMVar_hsa_circ_242547,RMVar_hsa_circ_107418,RMVar_hsa_circ_365634,RMVar_hsa_circ_366641,RMVar_hsa_circ_360725,RMVar_hsa_circ_288730,RMVar_hsa_circ_125692,RMVar_hsa_circ_283533,RMVar_hsa_circ_111332,RMVar_hsa_circ_92810,RMVar_hsa_circ_101695,RMVar_hsa_circ_83401,RMVar_hsa_circ_242551,RMVar_hsa_circ_242555,RMVar_hsa_circ_242557,RMVar_hsa_circ_242559,RMVar_hsa_circ_75824,RMVar_hsa_circ_242558,RMVar_hsa_circ_242556,RMVar_hsa_circ_242553,RMVar_hsa_circ_242554,RMVar_hsa_circ_242552,RMVar_hsa_circ_106096,RMVar_hsa_circ_242550,RMVar_hsa_circ_344061,RMVar_hsa_circ_276425,RMVar_hsa_circ_242565,RMVar_hsa_circ_242566,RMVar_hsa_circ_242567 114124 RMVar_ID_114124 Human_SNP_ID_866820091 m1A Human chr6 + 43516044 43516044 43516044 CTGATGCAGCTCACCCATATCCTCGAAGCTAGAGCCTGAGGTATCATCCATGTTCTCCATGTCAA CTGATGCAGCTCACCCATATCCTCGAAGCTAGCGCCTGAGGTATCATCCATGTTCTCCATGTCAA A C POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43515601..43516134 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114125 RMVar_ID_114125 Human_SNP_ID_866834370 m1A Human chr6 - 116279463 116279462 116279463 TGTGGTGATGGCAGCCGACCGCAGCCTGAAAAAGGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA TGTGGTGATGGCAGCCGACCGCAGCCTGAAAA_GGGCGTTCAGGGTGGAGAGAAGGCCCTAGAAA CT C TSPYL1 Ensembl:ENSG00000189241 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr6:116279251..116279562 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_1324070,Human_RBP_ID_18852236 114126 RMVar_ID_114126 Human_SNP_ID_866845964 m1A Human chr6 + 30737030 30737030 30737030 CCACTGTGCTTTCAGTTCTCTTCTGTGTCTCCATCGTGACCACACAAACCCTTTGTGATCTGGCC CCACTGTGCTTTCAGTTCTCTTCTGTGTCTCCGTCGTGACCACACAAACCCTTTGTGATCTGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:30737028..30737230 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114127 RMVar_ID_114127 Human_SNP_ID_866852371 m1A Human chr6 + 30649612 30649612 30649612 TACCATTCCCACCCCTTTGGCCCCACTCCACGACAACCACTTCCCCATCTTCTCCTCTATTCTGG TACCATTCCCACCCCTTTGGCCCCACTCCACGGCAACCACTTCCCCATCTTCTCCTCTATTCTGG A G C6orf136 Ensembl:ENSG00000204564 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr6:30649548..30649766;chr6:30647826..30649834 26863196 MeRIP-seq:(Medium) rs117013517 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_RBP_ID_17421506,Human_RBP_ID_18958078,Human_RBP_ID_27526942 Human_Splice_Rec_749352,Human_Splice_Rec_749362,Human_Splice_Rec_749372,Human_Splice_Rec_749386,Human_Splice_Rec_749406,Human_Splice_Rec_749408 114128 RMVar_ID_114128 Human_SNP_ID_866859137 m1A Human chr6 - 158637850 158637850 158637850 GCAATTGGTGGTAACGCTTATCAACACAGCAAAGTGAACCAGTGGACCACAAATGTAGTAGAACA GCAATTGGTGGTAACGCTTATCAACACAGCAATGTGAACCAGTGGACCACAAATGTAGTAGAACA T A DYNLT1 Ensembl:ENSG00000146425 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:158637751..158641375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_656289,Human_RBP_ID_947957,Human_RBP_ID_1666342,Human_RBP_ID_2012969,Human_RBP_ID_4905629,Human_RBP_ID_9401356,Human_RBP_ID_15712423,Human_RBP_ID_27829045 Human_Splice_Rec_828468,Human_Splice_Rec_828472,Human_Splice_Rec_828473,Human_Splice_Rec_828480 Human_miRNA_ID_2968200 RMVar_hsa_circ_26599,RMVar_hsa_circ_242763,RMVar_hsa_circ_242762,RMVar_hsa_circ_92200,RMVar_hsa_circ_242765,RMVar_hsa_circ_276300,RMVar_hsa_circ_281816,RMVar_hsa_circ_242764 114129 RMVar_ID_114129 Human_SNP_ID_866877285 m1A Human chr6 - 10410031 10410031 10410031 GCTCCTGCACACGCACCGGGGGCTGCCTCACCAGCTGTCGGGCCTGGATCCTCGCAGGGACTACA GCTCCTGCACACGCACCGGGGGCTGCCTCACCTGCTGTCGGGCCTGGATCCTCGCAGGGACTACA T A TFAP2A Ensembl:ENSG00000137203 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr6:10409930..10410031 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_4858409,Human_RBP_ID_5427689,Human_RBP_ID_15579763,Human_RBP_ID_18850393 RMVar_hsa_circ_2896 114130 RMVar_ID_114130 Human_SNP_ID_866905011 m1A Human chr6 - 31784713 31784713 31784713 ATCTCTCTGACTTCTCCCTCCTCCACCCCAGAAACTCTCAGCAGCTGTGACAGAGGCCTTTGTCC ATCTCTCTGACTTCTCCCTCCTCCACCCCAGACACTCTCAGCAGCTGTGACAGAGGCCTTTGTCC T G VARS1 Ensembl:ENSG00000204394 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:31784663..31784736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_949286,Human_RBP_ID_4882159,Human_RBP_ID_18195483,Human_RBP_ID_19016694,Human_RBP_ID_26829419 Human_Splice_Rec_754580,Human_Splice_Rec_754690 RMVar_hsa_circ_93604,RMVar_hsa_circ_266571,RMVar_hsa_circ_237832 114131 RMVar_ID_114131 Human_SNP_ID_866937335 m1A Human chr6 - 42335800 42335800 42335800 AGATGGAGTAGAGGAAACTATGTCAGCACGCAATGGAAGCTAGACTTTGTTTTGGGGAGTCAGAG AGATGGAGTAGAGGAAACTATGTCAGCACGCAGTGGAAGCTAGACTTTGTTTTGGGGAGTCAGAG T C TRERF1 Ensembl:ENSG00000124496 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:42335794..42335859 26863196 MeRIP-seq:(Medium) rs538536017 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_11291,RMVar_hsa_circ_238367 114132 RMVar_ID_114132 Human_SNP_ID_866969722 m1A Human chr6 + 134174800 134174800 134174800 AAGTGAGGGTGCCCTTAGCAGCCTCAGTTTTCACCGTCATCACCACCGCGGGGAGACAGAAAGAC AAGTGAGGGTGCCCTTAGCAGCCTCAGTTTTCGCCGTCATCACCACCGCGGGGAGACAGAAAGAC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr6:134174696..134174875;chr6:134174702..134174850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 6 haematopoietic and lymphoid tissue 114133 RMVar_ID_114133 Human_SNP_ID_866972155 m1A Human chr6 - 32976410 32976410 32976410 GGAGCTGCAGTAACAGCAAGGAGCGGGGGTCCAGCAGAGTGCAAGGACTTGAGAAGTGGAGAGGA GGAGCTGCAGTAACAGCAAGGAGCGGGGGTCCCGCAGAGTGCAAGGACTTGAGAAGTGGAGAGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:32976279..32976487 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114134 RMVar_ID_114134 Human_SNP_ID_867000907 m1A Human chr6 - 31356805 31356805 31356805 CGAGTCCGAGAGAGGAGCCGCGGGCGCCGTGGATAGAGCAGGAGGGGCCGGAGTATTGGGACCGG CGAGTCCGAGAGAGGAGCCGCGGGCGCCGTGGGTAGAGCAGGAGGGGCCGGAGTATTGGGACCGG T C HLA-B Ensembl:ENSG00000234745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr6:31356647..31356865;chr6:31356695..31356994 26863196 MeRIP-seq:(Medium) rs145974360 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,head_neck squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_661288,Human_RBP_ID_24156744 114135 RMVar_ID_114135 Human_SNP_ID_867006917 m1A Human chr6 - 34757553 34757553 34757553 TACGATCACCCTCAGATTTCGGGGCCCCACTCACTTGGGCATGTTGCTCTGCAGGCCGTTGGCCA TACGATCACCCTCAGATTTCGGGGCCCCACTCGCTTGGGCATGTTGCTCTGCAGGCCGTTGGCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr6:34757529..34757670 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114136 RMVar_ID_114136 Human_SNP_ID_867010768 m1A Human chr6 - 125302002 125302002 125302002 GAGTAAGAGGAGGGGGAAGAAAGACAAGGGGAAGGGGAGGAGGAGGAGGACGGGGAGGAGCTTCG GAGTAAGAGGAGGGGGAAGAAAGACAAGGGGAGGGGGAGGAGGAGGAGGACGGGGAGGAGCTTCG T C HDDC2 Ensembl:ENSG00000111906 Protein coding 5'UTR GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs1310679184 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_13536,Human_RBP_ID_947876,Human_RBP_ID_5152237,Human_RBP_ID_5327217,Human_RBP_ID_8944034,Human_RBP_ID_9437884,Human_RBP_ID_22462883,Human_RBP_ID_26355539 114137 RMVar_ID_114137 Human_SNP_ID_867015000 m1A Human chr6 - 31640436 31640436 31640436 CCTCCTGCTCCTGAGGGGGGCTCCCGGGATGAACAGGATGGAGCTTCAGCTGAGACAGAACCTTG CCTCCTGCTCCTGAGGGGGGCTCCCGGGATGAGCAGGATGGAGCTTCAGCTGAGACAGAACCTTG T C BAG6 Ensembl:ENSG00000204463 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:31640376..31640973 32194978 MeRIP-seq:(Medium) rs1195220483 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 7 liver Human_RBP_ID_661560,Human_RBP_ID_3806288,Human_RBP_ID_8642218,Human_RBP_ID_8900210,Human_RBP_ID_15786737,Human_RBP_ID_17663609,Human_RBP_ID_22461077 Human_Splice_Rec_752621,Human_Splice_Rec_752638,Human_Splice_Rec_752639,Human_Splice_Rec_752684,Human_Splice_Rec_752685,Human_Splice_Rec_752732,Human_Splice_Rec_752733,Human_Splice_Rec_752778,Human_Splice_Rec_752779,Human_Splice_Rec_752826,Human_Splice_Rec_752827 114138 RMVar_ID_114138 Human_SNP_ID_867060117 m1A Human chr6 - 132401342 132401342 132401342 CGGGGGGCTCGGGCCGAACCTATCCGCACCGGACCCTCCTGGACTCGGAGGGCAAGTACTGGCTG CGGGGGGCTCGGGCCGAACCTATCCGCACCGGGCCCTCCTGGACTCGGAGGGCAAGTACTGGCTG T C MOXD1 Ensembl:ENSG00000079931 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr6:132401294..132401445 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - Human_RBP_ID_4907146 Human_miRNA_ID_2992701 RMVar_hsa_circ_78517,RMVar_hsa_circ_241559 114139 RMVar_ID_114139 Human_SNP_ID_867077337 m1A Human chr6 + 17706303 17706303 17706303 CCATACCTGATGCTGTTGTCGCCCCTGCTGGTAAGGCTTAATTGGCCCCTGGTGGCAACGCCGCG CCATACCTGATGCTGTTGTCGCCCCTGCTGGTCAGGCTTAATTGGCCCCTGGTGGCAACGCCGCG A C AL138724.2 Ensembl:ENSG00000272269 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr6:17706276..17706475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 114140 RMVar_ID_114140 Human_SNP_ID_867080196 m1A Human chr6 - 35475671 35475671 35475671 GACCTCAACAGCACCATCCAGGAGGGCCCGGGAGCCTTCTATGGGGTCAGCTCTCAGTACAGCTC GACCTCAACAGCACCATCCAGGAGGGCCCGGGGGCCTTCTATGGGGTCAGCTCTCAGTACAGCTC T C TEAD3 Ensembl:ENSG00000007866 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:35475626..35475675 32194978 MeRIP-seq:(Medium) rs992013336 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_Splice_Rec_764602,Human_Splice_Rec_764626,Human_Splice_Rec_764650 RMVar_hsa_circ_15852,RMVar_hsa_circ_8780 114141 RMVar_ID_114141 Human_SNP_ID_867084858 m1A Human chr6 - 32180297 32180294 32180297 AGCTCAAATACTGAGCAGCCAAAAAAAGAAGAAGATGGCGAGAAACAGGAAGAGGGAATCCTGCC AGCTCAAATACTGAGCAGCCAAAAAAAGAAGA___TGGCGAGAAACAGGAAGAGGGAATCCTGCC ATCT A RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr6:32180246..32180366 26863196 MeRIP-seq:(Medium) rs752683365 Functional Loss DEL TCGA 33..35 33 OV 1 - 114142 RMVar_ID_114142 Human_SNP_ID_867094366 m1A Human chr6 - 43013355 43013353 43013356 CCTGCCCGGATGGCAACAGTAGTTCTAGGAGGAGACACCATGGGCCCTGAGCGTATCTTCCCCAA CCTGCCCGGATGGCAACAGTAGTTCTAGGAG___ACACCATGGGCCCTGAGCGTATCTTCCCCAA TCTC T MEA1 Ensembl:ENSG00000124733 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr6:43013126..43013400 26863196 MeRIP-seq:(Medium) rs749948541 Functional Loss DEL TCGA,ICGC 32..34 33 PBCA,UCEC 2 - Human_RBP_ID_664843,Human_RBP_ID_792113,Human_RBP_ID_1673578,Human_RBP_ID_2021571,Human_RBP_ID_4903329,Human_RBP_ID_5152186,Human_RBP_ID_7608182,Human_RBP_ID_9400556,Human_RBP_ID_15830705,Human_RBP_ID_17536320,Human_RBP_ID_26355181 Human_Splice_Rec_770902,Human_Splice_Rec_770908,Human_Splice_Rec_770914,Human_Splice_Rec_770920,Human_Splice_Rec_770926 Human_miRNA_ID_2353133,Human_miRNA_ID_2572652,Human_miRNA_ID_2909161 RMVar_hsa_circ_238521,RMVar_hsa_circ_346184,RMVar_hsa_circ_376870 114143 RMVar_ID_114143 Human_SNP_ID_867097912 m1A Human chr6 - 138404446 138404446 138404446 TGGGAGCCTGGTCAGCCGCGCAGAGGCCCCGCACCCCGGGCCGCCCCGCCTGCGTGTGCGCGCCC TGGGAGCCTGGTCAGCCGCGCAGAGGCCCCGCCCCCCGGGCCGCCCCGCCTGCGTGTGCGCGCCC T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr6:138404285..138404575 26863410 MeRIP-seq:(Medium) rs991765585 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114144 RMVar_ID_114144 Human_SNP_ID_867117855 m1A Human chr6 + 13711236 13711236 13711236 CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGAGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC CCGCTGGCGGGGGCAGCCGCTGAGGCAGGGGGGGGCGGGGGCGGCGGCGGGGGCGGCGGGGCCGC A G RF00017-4486,RF00017-5280 RNACentral:URS000090F764,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr6:13711079..13711357;chr6:13711163..13711564 26863196,26863410 MeRIP-seq:(Medium) rs989477384 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 114145 RMVar_ID_114145 Human_SNP_ID_867129855 m1A Human chr6 - 43038646 43038643 43038647 GAGTCTGCTGGCGTTCTCAGGGCTCTCCGCAGACATGCTCAATCAGGCGATTGGGCCCCTCACCT GAGTCTGCTGGCGTTCTCAGGGCTCTCCGCA____TGCTCAATCAGGCGATTGGGCCCCTCACCT ATGTC A CUL7 Ensembl:ENSG00000044090 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr6:43038601..43038675 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 32..35 33 SARC 2 - Human_RBP_ID_9350228 Human_Splice_Rec_771052,Human_Splice_Rec_771053,Human_Splice_Rec_771102,Human_Splice_Rec_771103,Human_Splice_Rec_771142,Human_Splice_Rec_771143,Human_Splice_Rec_771192,Human_Splice_Rec_771193,Human_Splice_Rec_771242,Human_Splice_Rec_771243,Human_Splice_Rec_771278,Human_Splice_Rec_771279,Human_Splice_Rec_771326,Human_Splice_Rec_771327 Human_miRNA_ID_2978814 RMVar_hsa_circ_79942,RMVar_hsa_circ_99068,RMVar_hsa_circ_126723,RMVar_hsa_circ_238533,RMVar_hsa_circ_76231,RMVar_hsa_circ_238534,RMVar_hsa_circ_238532,RMVar_hsa_circ_107299,RMVar_hsa_circ_127468,RMVar_hsa_circ_238536,RMVar_hsa_circ_238538,RMVar_hsa_circ_84568,RMVar_hsa_circ_238539,RMVar_hsa_circ_238537 114146 RMVar_ID_114146 Human_SNP_ID_867134222 m1A Human chr6 - 63576465 63576465 63576465 CAGTAATCTCCACTGCCCTTCAGAAACTCCATAAATGTGTGACCAAGAACACCACAGAATTGCTG CAGTAATCTCCACTGCCCTTCAGAAACTCCATGAATGTGTGACCAAGAACACCACAGAATTGCTG T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr6:63576426..63576475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114147 RMVar_ID_114147 Human_SNP_ID_834046665 m1A Human chr2 + 740204 740204 740204 GGAGAGGCCCGGAGGATCTTCCCTCAGAGCCTAGCGAGGGAGCGCGGCCCAGCCAGGAGAGCTGG GGAGAGGCCCGGAGGATCTTCCCTCAGAGCCTGGCGAGGGAGCGCGGCCCAGCCAGGAGAGCTGG A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740169..740290 26863196 MeRIP-seq:(Medium) rs1194649331 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114148 RMVar_ID_114148 Human_SNP_ID_834063803 m1A Human chr2 - 206160006 206160006 206160006 GCCAGGTAATCGTTGAGCACCTGGAGGCCGGCAGGGCTTTTCAGGTCTCCGAAACCCATGGTGTC GCCAGGTAATCGTTGAGCACCTGGAGGCCGGCGGGGCTTTTCAGGTCTCCGAAACCCATGGTGTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:206159878..206160769 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 114149 RMVar_ID_114149 Human_SNP_ID_834091003 m1A Human chr2 - 3448619 3448587 3448619 CCACGCCCTACCCTCGCGTAACCGGCTGCTCTAGACGCCCTACCCTCGAGTAACCGGCTGCTCTC CCACGCCCTACCCTCGCGTAACCGGCTGCTCT________________________________C GAGAGCAGCCGGTTACTCGAGGGTAGGGCGTCT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:3448509..3448661;chr2:3448537..3448800 26863196 MeRIP-seq:(Medium) rs1289963608 Functional Loss DEL ICGC 33..64 33 CHOL 1 - 114150 RMVar_ID_114150 Human_SNP_ID_834096247 m1A Human chr2 - 130172396 130172396 130172396 TGGTTCCTGCCCACCGAAGGCAGTGTGCCCCCACCACTCTCCTCCAGCCCAGGGGGGACCAGCCC TGGTTCCTGCCCACCGAAGGCAGTGTGCCCCCTCCACTCTCCTCCAGCCCAGGGGGGACCAGCCC T A SMPD4 Ensembl:ENSG00000136699 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130172326..130172419 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_17393024,Human_RBP_ID_17509747,Human_RBP_ID_17939606 Human_Splice_Rec_296649,Human_Splice_Rec_296683,Human_Splice_Rec_296721,Human_Splice_Rec_296785,Human_Splice_Rec_296835,Human_Splice_Rec_296873,Human_Splice_Rec_296925,Human_Splice_Rec_296935,Human_Splice_Rec_296949 RMVar_hsa_circ_45265,RMVar_hsa_circ_94324,RMVar_hsa_circ_203235,RMVar_hsa_circ_42299,RMVar_hsa_circ_56404,RMVar_hsa_circ_365958,RMVar_hsa_circ_47036,RMVar_hsa_circ_5334,RMVar_hsa_circ_286308,RMVar_hsa_circ_203237 114151 RMVar_ID_114151 Human_SNP_ID_834135645 m1A Human chr2 - 73926943 73926943 73926943 GGGCTCTTGGCCATGGAACTGAAGGGTGCTCGAAGCCGACTTAGAAAGAGGCGGCCCGCGGCCAT GGGCTCTTGGCCATGGAACTGAAGGGTGCTCGGAGCCGACTTAGAAAGAGGCGGCCCGCGGCCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73926893..73927000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine 114152 RMVar_ID_114152 Human_SNP_ID_834138101 m1A Human chr2 - 229180852 229180852 229180852 TGAGAGATGGGCGAGCGCCGTTCCGAAGGGACAGGCAATGGCCTCCCTTGCCCTCAGCGGATCGA TGAGAGATGGGCGAGCGCCGTTCCGAAGGGACGGGCAATGGCCTCCCTTGCCCTCAGCGGATCGA T C PID1 Ensembl:ENSG00000153823 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:229180803..229180885 26863196 MeRIP-seq:(Medium) rs62190429 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,frontal_lobe astrocytoma_Grade_III,LMS,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_II,frontal_lobe oligodendroglioma_Grade_III 16 brain Human_RBP_ID_270321,Human_RBP_ID_280687,Human_RBP_ID_545430,Human_RBP_ID_1022178,Human_RBP_ID_1098470,Human_RBP_ID_1134600,Human_RBP_ID_1197384,Human_RBP_ID_1303007,Human_RBP_ID_1379511,Human_RBP_ID_1584090,Human_RBP_ID_1912150,Human_RBP_ID_2673800,Human_RBP_ID_3617518,Human_RBP_ID_4598728,Human_RBP_ID_5194502,Human_RBP_ID_5262753,Human_RBP_ID_5275692,Human_RBP_ID_5422822,Human_RBP_ID_5444560,Human_RBP_ID_5470502,Human_RBP_ID_5501764,Human_RBP_ID_5589061,Human_RBP_ID_6893348,Human_RBP_ID_8107428,Human_RBP_ID_8260212,Human_RBP_ID_8513414,Human_RBP_ID_8846057,Human_RBP_ID_9103676,Human_RBP_ID_9259413,Human_RBP_ID_9295599,Human_RBP_ID_9975034,Human_RBP_ID_10484019,Human_RBP_ID_13789207,Human_RBP_ID_17015051,Human_RBP_ID_17063692,Human_RBP_ID_17068870,Human_RBP_ID_17135123,Human_RBP_ID_17192638,Human_RBP_ID_17280429,Human_RBP_ID_17390490,Human_RBP_ID_17506341,Human_RBP_ID_17698608,Human_RBP_ID_17951812,Human_RBP_ID_18180894,Human_RBP_ID_18200861,Human_RBP_ID_18208876,Human_RBP_ID_18315185,Human_RBP_ID_18443157,Human_RBP_ID_18515593,Human_RBP_ID_18534326,Human_RBP_ID_18755489,Human_RBP_ID_20534620,Human_RBP_ID_21931272,Human_RBP_ID_22006703,Human_RBP_ID_22248432,Human_RBP_ID_22393209,Human_RBP_ID_22422690,Human_RBP_ID_22505170,Human_RBP_ID_22816686,Human_RBP_ID_22990011,Human_RBP_ID_23133404,Human_RBP_ID_23182310,Human_RBP_ID_23281294,Human_RBP_ID_23311136,Human_RBP_ID_23855889,Human_RBP_ID_24533340,Human_RBP_ID_24540265,Human_RBP_ID_25518917,Human_RBP_ID_26480236,Human_RBP_ID_26663912,Human_RBP_ID_26749885,Human_RBP_ID_27007556,Human_RBP_ID_27158802,Human_RBP_ID_27287271,Human_RBP_ID_27478137,Human_RBP_ID_27563619,Human_RBP_ID_27693373 RMVar_hsa_circ_354719,RMVar_hsa_circ_361298,RMVar_hsa_circ_207384 114153 RMVar_ID_114153 Human_SNP_ID_834145564 m1A Human chr2 - 96305437 96305437 96305437 TGGTGGTCTGAAGCCTCCGAGCAGCCGCGGCCATGGCGGATGTAACCGCCCGTAGTCTGCAATAC TGGTGGTCTGAAGCCTCCGAGCAGCCGCGGCCGTGGCGGATGTAACCGCCCGTAGTCTGCAATAC T C SNRNP200 Ensembl:ENSG00000144028 Protein coding start codon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:96305354..96305525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_4620928,Human_RBP_ID_5322121,Human_RBP_ID_5528650,Human_RBP_ID_8851468,Human_RBP_ID_9259883,Human_RBP_ID_9296768,Human_RBP_ID_9331092,Human_RBP_ID_9384288,Human_RBP_ID_22720663,Human_RBP_ID_24553273,Human_RBP_ID_26338635,Human_RBP_ID_27016566,Human_RBP_ID_27573331,Human_RBP_ID_27817355 Human_Splice_Rec_274821,Human_Splice_Rec_275001 RMVar_hsa_circ_88869,RMVar_hsa_circ_201843,RMVar_hsa_circ_201875,RMVar_hsa_circ_111395 114154 RMVar_ID_114154 Human_SNP_ID_834149126 m1A Human chr2 + 127293602 127293602 127293602 CTTGGCTCCATATTCATCCACTTTGGTGCCTGACTCATCCACCTGCTTCCCCGCCGCCGAGGGAA CTTGGCTCCATATTCATCCACTTTGGTGCCTGGCTCATCCACCTGCTTCCCCGCCGCCGAGGGAA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:127293551..127293755 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 114155 RMVar_ID_114155 Human_SNP_ID_834179658 m1A Human chr2 + 9843619 9843617 9843620 ACGATCGCCGGGGCCGGAGGAGAGAGAAGCTGAGGAGGAGCGGCGGAGGACGCCGCGGGTTGGGG ACGATCGCCGGGGCCGGAGGAGAGAGAAGCT___GAGGAGCGGCGGAGGACGCCGCGGGTTGGGG TGAG T TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:9843579..9843743 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 STAD 1 - 114156 RMVar_ID_114156 Human_SNP_ID_834188043 m1A Human chr2 - 39437141 39437141 39437141 CCGCTTGTCGTCGTCCGCAGCGGCGTGAGGGGAGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGAG CCGCTTGTCGTCGTCCGCAGCGGCGTGAGGGGGGCGGCGGCGGCGGCGGCGGCCGCAGCGTGGAG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr2:39437092..39437312;chr2:39436986..39437246 26863196 MeRIP-seq:(Medium) rs1402931465 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_777799,Human_RBP_ID_9330990,Human_RBP_ID_9386395,Human_RBP_ID_18421746,Human_RBP_ID_22077036,Human_RBP_ID_22597969,Human_RBP_ID_22997134,Human_RBP_ID_26770142,Human_RBP_ID_27817027 114157 RMVar_ID_114157 Human_SNP_ID_834203843 m1A Human chr2 + 32916334 32916334 32916334 GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGAGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG GGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGGTGGGAGGGGGGGGTGAGAGGGGGGGGGGGGGGG A T LINC00486 Ensembl:ENSG00000230876 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:32916170..32916671 26863196 MeRIP-seq:(Medium) rs878960983 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8258896,Human_RBP_ID_17068883 114158 RMVar_ID_114158 Human_SNP_ID_834245875 m1A Human chr2 - 238064308 238064308 238064308 AAAGACACCCATTAAGGAAAAGGAGATGGCATATGGGAAATATGGCTGCTCTGTGTCTATCCCAT AAAGACACCCATTAAGGAAAAGGAGATGGCATGTGGGAAATATGGCTGCTCTGTGTCTATCCCAT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:238064306..238064409 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114159 RMVar_ID_114159 Human_SNP_ID_834261097 m1A Human chr2 + 32618228 32618224 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTAT____TTTTTTTTTTACTATAGAGTGAGGGGTTGTTA TTTTA T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1559168925 Functional Loss DEL TCGA 30..33 33 UCEC,THYM 5 - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 114160 RMVar_ID_114160 Human_SNP_ID_834264472 m1A Human chr2 - 241249890 241249890 241249890 GAGCAATTTGATCCGCATCGAGGGGGACCCACAGGGCGTGCAGCAGGCCAAGCGAGAGCTGCTGG GAGCAATTTGATCCGCATCGAGGGGGACCCACGGGGCGTGCAGCAGGCCAAGCGAGAGCTGCTGG T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241249819..241249941 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_57679,Human_RBP_ID_775300,Human_RBP_ID_829685,Human_RBP_ID_922582,Human_RBP_ID_1913714,Human_RBP_ID_2632335,Human_RBP_ID_3620104,Human_RBP_ID_6900789,Human_RBP_ID_8847010,Human_RBP_ID_9385875,Human_RBP_ID_26340526,Human_RBP_ID_27819470 Human_Splice_Rec_381278,Human_Splice_Rec_381279,Human_Splice_Rec_381332,Human_Splice_Rec_381333,Human_Splice_Rec_381386,Human_Splice_Rec_381387,Human_Splice_Rec_381440,Human_Splice_Rec_381441,Human_Splice_Rec_381473,Human_Splice_Rec_381510,Human_Splice_Rec_381511,Human_Splice_Rec_381614,Human_Splice_Rec_381615,Human_Splice_Rec_381618,Human_Splice_Rec_381619,Human_Splice_Rec_381624,Human_Splice_Rec_381625 Human_miRNA_ID_2510886,Human_miRNA_ID_3053708 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_323740,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_208057,RMVar_hsa_circ_208056,RMVar_hsa_circ_208062,RMVar_hsa_circ_87225,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_352648,RMVar_hsa_circ_6493,RMVar_hsa_circ_54737,RMVar_hsa_circ_113630,RMVar_hsa_circ_78553,RMVar_hsa_circ_92839,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_82300,RMVar_hsa_circ_89716,RMVar_hsa_circ_208077,RMVar_hsa_circ_208078,RMVar_hsa_circ_208076,RMVar_hsa_circ_58489,RMVar_hsa_circ_353105,RMVar_hsa_circ_303265,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_208080,RMVar_hsa_circ_62923,RMVar_hsa_circ_304508,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,RMVar_hsa_circ_20061,RMVar_hsa_circ_208084,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_354726,RMVar_hsa_circ_63419,RMVar_hsa_circ_359290,RMVar_hsa_circ_208085,RMVar_hsa_circ_329999,RMVar_hsa_circ_48205,RMVar_hsa_circ_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_208087,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 114161 RMVar_ID_114161 Human_SNP_ID_834267436 m1A Human chr2 + 226796175 226796175 226796175 GATCCCCCAGGGACAGCCTCGTGGGCCGGGCCAGGCGGCTATTGGTCTGAGCAGCTGTGTCCACC GATCCCCCAGGGACAGCCTCGTGGGCCGGGCCGGGCGGCTATTGGTCTGAGCAGCTGTGTCCACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:226796126..226796425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder 114162 RMVar_ID_114162 Human_SNP_ID_834290032 m1A Human chr2 + 219387821 219387821 219387821 GCTCATCTGGCCTCCGGGCTCGGCCCGCCCCCACCGCGCCGCCTGCCCCGCCCCTCACTAGCTTT GCTCATCTGGCCTCCGGGCTCGGCCCGCCCCCCCCGCGCCGCCTGCCCCGCCCCTCACTAGCTTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219387602..219387925 26863196 MeRIP-seq:(Medium) rs933057081 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114163 RMVar_ID_114163 Human_SNP_ID_834299384 m1A Human chr2 + 54646474 54646474 54646474 GGAGCTGTACATGATGTCAGAGGAGAAGGCCAAGGTGAGAGGAGGCGGGAAGCATCCCTGTCCCA GGAGCTGTACATGATGTCAGAGGAGAAGGCCACGGTGAGAGGAGGCGGGAAGCATCCCTGTCCCA A C SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:54646351..54646511 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_922018,Human_RBP_ID_8851247,Human_RBP_ID_9296536,Human_RBP_ID_9383746,Human_RBP_ID_19097430,Human_RBP_ID_26339310,Human_RBP_ID_26667036 Human_Splice_Rec_245789,Human_Splice_Rec_245859,Human_Splice_Rec_245951 RMVar_hsa_circ_59575,RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_199905,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_68989,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_199916 114164 RMVar_ID_114164 Human_SNP_ID_834311319 m1A Human chr2 - 110674314 110674314 110674314 CAGAGCTACAAGGGCAATGACCCTCTTGGTGAATGGGAAAGGTCAGCATTTAGTTATTTTATTTC CAGAGCTACAAGGGCAATGACCCTCTTGGTGAGTGGGAAAGGTCAGCATTTAGTTATTTTATTTC T C BUB1 Ensembl:ENSG00000169679 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:110674301..110674375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_532031,Human_RBP_ID_4623557,Human_RBP_ID_18744330 Human_Splice_Rec_286752,Human_Splice_Rec_286753,Human_Splice_Rec_286858,Human_Splice_Rec_286859,Human_Splice_Rec_286912,Human_Splice_Rec_286913,Human_Splice_Rec_286950,Human_Splice_Rec_286951,Human_Splice_Rec_286970,Human_Splice_Rec_286971,Human_Splice_Rec_286996,Human_Splice_Rec_286997,Human_Splice_Rec_287006,Human_Splice_Rec_287007,Human_Splice_Rec_287013 Human_miRNA_ID_2948409,Human_miRNA_ID_2948410,Human_miRNA_ID_2948411,Human_miRNA_ID_2948412 RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500,RMVar_hsa_circ_110025,RMVar_hsa_circ_114948,RMVar_hsa_circ_202503,RMVar_hsa_circ_202502,RMVar_hsa_circ_300813,RMVar_hsa_circ_202519,RMVar_hsa_circ_291477,RMVar_hsa_circ_4533,RMVar_hsa_circ_333857 114165 RMVar_ID_114165 Human_SNP_ID_834317495 m1A Human chr2 - 241239969 241239969 241239969 CTGCGGCTGAGGACAAGGACCAGGACCTGATCACCATCATTGGAAAGGAGGACGCCGTCCGAGAG CTGCGGCTGAGGACAAGGACCAGGACCTGATCGCCATCATTGGAAAGGAGGACGCCGTCCGAGAG T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241239642..241240103 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_57672,Human_RBP_ID_242118,Human_RBP_ID_546998,Human_RBP_ID_1584886,Human_RBP_ID_1913690,Human_RBP_ID_5194544,Human_RBP_ID_6900756,Human_RBP_ID_8515572,Human_RBP_ID_8846987,Human_RBP_ID_9385854,Human_RBP_ID_13820995,Human_RBP_ID_17275581,Human_RBP_ID_17390732,Human_RBP_ID_18193574,Human_RBP_ID_18533540,Human_RBP_ID_18757212,Human_RBP_ID_26340517,Human_RBP_ID_27009063,Human_RBP_ID_27478807 Human_Splice_Rec_381291,Human_Splice_Rec_381345,Human_Splice_Rec_381399,Human_Splice_Rec_381453,Human_Splice_Rec_381485,Human_Splice_Rec_381523,Human_Splice_Rec_381575,Human_Splice_Rec_381583,Human_Splice_Rec_381589 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_27144,RMVar_hsa_circ_107101,RMVar_hsa_circ_323740,RMVar_hsa_circ_208054,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_113256,RMVar_hsa_circ_208057,RMVar_hsa_circ_208058,RMVar_hsa_circ_208056,RMVar_hsa_circ_208062,RMVar_hsa_circ_87225,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_352648,RMVar_hsa_circ_79638,RMVar_hsa_circ_39483,RMVar_hsa_circ_60705,RMVar_hsa_circ_54737,RMVar_hsa_circ_113630,RMVar_hsa_circ_208068,RMVar_hsa_circ_78553,RMVar_hsa_circ_55360,RMVar_hsa_circ_92839,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_82300,RMVar_hsa_circ_89716,RMVar_hsa_circ_208077,RMVar_hsa_circ_208078,RMVar_hsa_circ_208076,RMVar_hsa_circ_63741,RMVar_hsa_circ_58489,RMVar_hsa_circ_353105,RMVar_hsa_circ_303265,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_36798,RMVar_hsa_circ_208080,RMVar_hsa_circ_62923 114166 RMVar_ID_114166 Human_SNP_ID_834337918 m1A Human chr2 - 74654435 74654435 74654435 GGCCGCTCAGCACCGCCAGCAGCAGTAGCGGGAAGGGCGAGGCTGTAGGCTGCCCGGGACCCGGG GGCCGCTCAGCACCGCCAGCAGCAGTAGCGGGGAGGGCGAGGCTGTAGGCTGCCCGGGACCCGGG T C lnc-M1AP-1 RNACentral:URS0000D5BE6E lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74654386..74654457 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 114167 RMVar_ID_114167 Human_SNP_ID_834355273 m1A Human chr2 - 240135079 240135079 240135079 ACCCAGATCGTGAAACCATCTGGAACCATGCTAAAGAGGGTGGCTCTGTGCACCCCGCTCCCGAA ACCCAGATCGTGAAACCATCTGGAACCATGCTCAAGAGGGTGGCTCTGTGCACCCCGCTCCCGAA T G COPS9 Ensembl:ENSG00000172428 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240135077..240135216 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 114168 RMVar_ID_114168 Human_SNP_ID_834382273 m1A Human chr2 + 20165126 20165126 20165126 CTCACCACACTCACCACACATACCACACTCACACCACACACATACCACATACCACACTCACCCCA CTCACCACACTCACCACACATACCACACTCACCCCACACACATACCACATACCACACTCACCCCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:20165105..20165170 26863196 MeRIP-seq:(Medium) rs532998720 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114169 RMVar_ID_114169 Human_SNP_ID_834405948 m1A Human chr2 + 96816354 96816354 96816354 CGCCGCGCTCTGCCTGGGCAACGCCGCGGGGGAGGCCGCGCCGGGCCCGCGAGTGCTGGGCTTCT CGCCGCGCTCTGCCTGGGCAACGCCGCGGGGGGGGCCGCGCCGGGCCCGCGAGTGCTGGGCTTCT A G CNNM3 Ensembl:ENSG00000168763 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,untreat control chr2:96816282..96816437;chr2:96816283..96816378 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_4621369,Human_RBP_ID_5322525,Human_RBP_ID_9330567,Human_RBP_ID_9353803,Human_RBP_ID_9387055,Human_RBP_ID_18470822,Human_RBP_ID_22077684,Human_RBP_ID_22451528 114170 RMVar_ID_114170 Human_SNP_ID_834409092 m1A Human chr2 + 96861648 96861648 96861648 GTCCGAGGTCATCACATGCTGGATCAGTAGAGATCTGGTAGGGGATGTAGGGTACATCAGCAGCC GTCCGAGGTCATCACATGCTGGATCAGTAGAGCTCTGGTAGGGGATGTAGGGTACATCAGCAGCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96861602..96861938 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 114171 RMVar_ID_114171 Human_SNP_ID_834458538 m1A Human chr2 + 168075166 168075166 168075166 CCTTCTTCGCTCTTCTCATCCATCTCGTCGTCACTCCACTCCCAGTCCCCGTCTTCGGTTTTATG CCTTCTTCGCTCTTCTCATCCATCTCGTCGTCGCTCCACTCCCAGTCCCCGTCTTCGGTTTTATG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:168075116..168075217 26863196 MeRIP-seq:(Medium) rs201897996 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114172 RMVar_ID_114172 Human_SNP_ID_834468649 m1A Human chr2 + 135724075 135724075 135724075 GCTCCGGGACCCCCAGTCCCAACCACGTCGTCACCCCCTCTGCTGTGGCAGTGGGGACAACACTG GCTCCGGGACCCCCAGTCCCAACCACGTCGTCGCCCCCTCTGCTGTGGCAGTGGGGACAACACTG A G R3HDM1 Ensembl:ENSG00000048991 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:135724051..135724075 26863196 MeRIP-seq:(Medium) rs548074075 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 7 caecum,large intestine Human_RBP_ID_142252,Human_RBP_ID_17279139,Human_RBP_ID_17392800,Human_RBP_ID_17509753 Human_miRNA_ID_2271447 RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_203453,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_203465 114173 RMVar_ID_114173 Human_SNP_ID_834556059 m1A Human chr2 + 174571959 174571959 174571959 GGAGGCTTGTTGTTCTGAGGAGGAGGAGGGGGAACCGCTTCCCTGTGGATGGAGGGCCTGTTGCC GGAGGCTTGTTGTTCTGAGGAGGAGGAGGGGGGACCGCTTCCCTGTGGATGGAGGGCCTGTTGCC A G AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174571674..174572450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus 114174 RMVar_ID_114174 Human_SNP_ID_834576585 m1A Human chr2 - 46612338 46612338 46612338 AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCATTGGAAACATTTTTATTTGCAGTTATTTTGTC AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCGTTGGAAACATTTTTATTTGCAGTTATTTTGTC T C PIGF Ensembl:ENSG00000151665 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1824050 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 3 head and neck Human_RBP_ID_22595243 Human_Splice_Rec_242140,Human_Splice_Rec_242158,Human_Splice_Rec_242168,Human_Splice_Rec_242174 RMVar_hsa_circ_199572,RMVar_hsa_circ_301100,RMVar_hsa_circ_369497,RMVar_hsa_circ_199573,RMVar_hsa_circ_199574,RMVar_hsa_circ_281678 114175 RMVar_ID_114175 Human_SNP_ID_834576586 m1A Human chr2 - 46612338 46612338 46612338 AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCATTGGAAACATTTTTATTTGCAGTTATTTTGTC AAAAAGTAATCTTTTTTTTTTTCTAGGTTGGCTTTGGAAACATTTTTATTTGCAGTTATTTTGTC T A PIGF Ensembl:ENSG00000151665 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_22595243 Human_Splice_Rec_242140,Human_Splice_Rec_242158,Human_Splice_Rec_242168,Human_Splice_Rec_242174 RMVar_hsa_circ_199572,RMVar_hsa_circ_301100,RMVar_hsa_circ_369497,RMVar_hsa_circ_199573,RMVar_hsa_circ_199574,RMVar_hsa_circ_281678 114176 RMVar_ID_114176 Human_SNP_ID_834583437 m1A Human chr2 + 130230790 130230790 130230790 CTGCTCTCGGGGAGCTCGGGGGCCTTCATCCCAGTGCTGCCTTTCATCCTGGAGATGTTCCAGCA CTGCTCTCGGGGAGCTCGGGGGCCTTCATCCCGGTGCTGCCTTTCATCCTGGAGATGTTCCAGCA A G NOC2LP1 Ensembl:ENSG00000213225 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1302849085 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114177 RMVar_ID_114177 Human_SNP_ID_834630815 m1A Human chr2 - 71070552 71070552 71070552 AGTGGTTTGTGCTCAGTCCATCTGCTTCTGCCAGGATCTTCCCATCCTCTGAGACTAAAAGGACC AGTGGTTTGTGCTCAGTCCATCTGCTTCTGCCCGGATCTTCCCATCCTCTGAGACTAAAAGGACC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:71070453..71070600;chr2:71070470..71070615;chr2:71070460..71070623 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 19 pancreas 114178 RMVar_ID_114178 Human_SNP_ID_834640589 m1A Human chr2 - 70293680 70293680 70293680 GGGAGCGTGAGGAAAGCCGTGCGTTGCGTTCCAAGGCATCTGTGAGCCCGCGGAGTATACACCAT GGGAGCGTGAGGAAAGCCGTGCGTTGCGTTCCGAGGCATCTGTGAGCCCGCGGAGTATACACCAT T C SNRPG Ensembl:ENSG00000143977 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:70293585..70293750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_146771,Human_RBP_ID_554731,Human_RBP_ID_777149,Human_RBP_ID_1589549,Human_RBP_ID_1922487,Human_RBP_ID_4615017,Human_RBP_ID_5118286,Human_RBP_ID_5146573,Human_RBP_ID_5322093,Human_RBP_ID_8524250,Human_RBP_ID_9110161,Human_RBP_ID_9330504,Human_RBP_ID_19097586,Human_RBP_ID_22426386,Human_RBP_ID_22451358,Human_RBP_ID_23882500,Human_RBP_ID_24376464,Human_RBP_ID_27014126,Human_RBP_ID_27564029 Human_Splice_Rec_258837,Human_Splice_Rec_258843,Human_Splice_Rec_258873,Human_Splice_Rec_258881,Human_Splice_Rec_258883 114179 RMVar_ID_114179 Human_SNP_ID_834692636 m1A Human chr2 - 219574991 219574991 219574991 AGCGCAGCAGCAGCACCAGGACGGGGTGGGTCAGCAGAGAGAGAGCAGAGGTGGCCAGGTGCAGC AGCGCAGCAGCAGCACCAGGACGGGGTGGGTCCGCAGAGAGAGAGCAGAGGTGGCCAGGTGCAGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:219574743..219575193 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 114180 RMVar_ID_114180 Human_SNP_ID_834696746 m1A Human chr2 + 210592928 210592928 210592928 CAAACCCTTCTTCGCTGTGCAGTTCCACCCAGAGGTCACCCCGGGGCCAATAGACACTGAGGTAC CAAACCCTTCTTCGCTGTGCAGTTCCACCCAGTGGTCACCCCGGGGCCAATAGACACTGAGGTAC A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210592846..210592954 26863196 MeRIP-seq:(Medium) rs756428203 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_55907,Human_RBP_ID_304446,Human_RBP_ID_8511007 Human_Splice_Rec_353102,Human_Splice_Rec_353103,Human_Splice_Rec_353180,Human_Splice_Rec_353181,Human_Splice_Rec_353256,Human_Splice_Rec_353257,Human_Splice_Rec_353332,Human_Splice_Rec_353333,Human_Splice_Rec_353406,Human_Splice_Rec_353407,Human_Splice_Rec_353480,Human_Splice_Rec_353481 Human_miRNA_ID_2423322,Human_miRNA_ID_2432982 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_348714,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_31823,RMVar_hsa_circ_21428,RMVar_hsa_circ_22952,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_72435,RMVar_hsa_circ_68775,RMVar_hsa_circ_59196,RMVar_hsa_circ_69514,RMVar_hsa_circ_70421,RMVar_hsa_circ_100412,RMVar_hsa_circ_70074,RMVar_hsa_circ_60244,RMVar_hsa_circ_55652,RMVar_hsa_circ_73167,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_60939,RMVar_hsa_circ_361168,RMVar_hsa_circ_69154,RMVar_hsa_circ_69776,RMVar_hsa_circ_80365,RMVar_hsa_circ_58119,RMVar_hsa_circ_70790,RMVar_hsa_circ_74265,RMVar_hsa_circ_84316,RMVar_hsa_circ_206568,RMVar_hsa_circ_206569,RMVar_hsa_circ_74078,RMVar_hsa_circ_366254 114181 RMVar_ID_114181 Human_SNP_ID_834699000 m1A Human chr2 + 740672 740672 740672 AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG AGCGTGGCGAGGGGGCGTGGCCCAGCCAGGAGGGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAG A G lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:740596..741063 26863196 MeRIP-seq:(Medium) rs113469378 Functional Loss SNV ICGC 33..33 33 COCA 1 - 114182 RMVar_ID_114182 Human_SNP_ID_834717519 m1A Human chr2 - 97792580 97792580 97792580 GCCACCGCCAGTGCCTCAGCCCCAGGAGCCGCAGCCTGAAAGGCTGTCTCCCGCCCCCCTCGCAC GCCACCGCCAGTGCCTCAGCCCCAGGAGCCGCTGCCTGAAAGGCTGTCTCCCGCCCCCCTCGCAC T A TMEM131 Ensembl:ENSG00000075568 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:97792531..97792651 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_242257 Human_miRNA_ID_3011246 RMVar_hsa_circ_110985,RMVar_hsa_circ_201991,RMVar_hsa_circ_34805,RMVar_hsa_circ_69249,RMVar_hsa_circ_4826,RMVar_hsa_circ_74875,RMVar_hsa_circ_25623,RMVar_hsa_circ_63301,RMVar_hsa_circ_64600,RMVar_hsa_circ_56246,RMVar_hsa_circ_201994 114183 RMVar_ID_114183 Human_SNP_ID_834717875 m1A Human chr2 + 74472625 74472625 74472625 AAGGGACAGAACTGAACCCGAACCTGTTTGACAGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC AAGGGACAGAACTGAACCCGAACCTGTTTGACTGGCCGCAGACCAAGCCGAGCCAAGGCAGCTGC A T AC005041.5 Ensembl:ENSG00000286883 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:74472099..74472675;chr2:74472454..74472675;chr2:74472432..74472675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung 114184 RMVar_ID_114184 Human_SNP_ID_834718793 m1A Human chr2 + 24084311 24084311 24084311 GTAGAGGTTTTCCGGTCCTCCCGGCTTGTCAAAGTGCACGGCTAACATATTGTCTGAGGACACAG GTAGAGGTTTTCCGGTCCTCCCGGCTTGTCAACGTGCACGGCTAACATATTGTCTGAGGACACAG A C FAM228B Ensembl:ENSG00000219626 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:24084260..24084432 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 4 lung 114185 RMVar_ID_114185 Human_SNP_ID_834719034 m1A Human chr2 - 127627280 127627280 127627280 ACCTGTTGGTGGCCAGACCCATGACCTCTGGGAAAGAGAGTTCCAGCAGCATCTTCTCCTGCTGG ACCTGTTGGTGGCCAGACCCATGACCTCTGGGTAAGAGAGTTCCAGCAGCATCTTCTCCTGCTGG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:127627229..127628391 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney 114186 RMVar_ID_114186 Human_SNP_ID_834735042 m1A Human chr2 + 189011630 189011630 189011630 TGATCATGTACATTTTGTCCTTTTTTACAGAAACACACTGGGGAATGGAGCAAAACAGTCTTTGA TGATCATGTACATTTTGTCCTTTTTTACAGAATCACACTGGGGAATGGAGCAAAACAGTCTTTGA A T COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:189011626..189011700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_Splice_Rec_336364,Human_Splice_Rec_336442,Human_Splice_Rec_336458 RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_205240,RMVar_hsa_circ_124579,RMVar_hsa_circ_205241,RMVar_hsa_circ_127071,RMVar_hsa_circ_109084,RMVar_hsa_circ_205243 114187 RMVar_ID_114187 Human_SNP_ID_834743207 m1A Human chr2 - 105336604 105336604 105336604 ATATTTTGCACATTTAAAACTTAAACTTGGGTATGGTGGCTTATGCCTGTAATCACGGCGTTTTG ATATTTTGCACATTTAAAACTTAAACTTGGGTGTGGTGGCTTATGCCTGTAATCACGGCGTTTTG T C AC012360.3 Ensembl:ENSG00000272994 lincRNA exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2679861 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_11815,GWAS_ID_11816,GWAS_ID_11817,GWAS_ID_11818,GWAS_ID_11819,GWAS_ID_11820 114188 RMVar_ID_114188 Human_SNP_ID_834804451 m1A Human chr2 + 46762123 46762123 46762123 CTTTTAAAGCAAAATGGGGATTGAAGGGACTTATAATTTCTGTTGTTTCTAATTAAAGTCCCTGA CTTTTAAAGCAAAATGGGGATTGAAGGGACTTTTAATTTCTGTTGTTTCTAATTAAAGTCCCTGA A T SOCS5,LINC01118 Ensembl:ENSG00000171150,Ensembl:ENSG00000222005 Protein coding,lincRNA 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17771942 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2648970,Human_RBP_ID_18317446 GWAS_ID_15297,GWAS_ID_15298,GWAS_ID_15299,GWAS_ID_15300,GWAS_ID_15301,GWAS_ID_15302,GWAS_ID_15303,GWAS_ID_15304,GWAS_ID_15305,GWAS_ID_15306,GWAS_ID_15307,GWAS_ID_15308,GWAS_ID_15309,GWAS_ID_15310,GWAS_ID_15311,GWAS_ID_15312,GWAS_ID_15313,GWAS_ID_15314,GWAS_ID_15315 114189 RMVar_ID_114189 Human_SNP_ID_834810566 m1A Human chr2 + 65071933 65071933 65071933 TTCCAGGCTGAGTACTGGGCCTGTGTGCTGCCAGATTCCCTGCCTCCATCACCCGACCGCCACTC TTCCAGGCTGAGTACTGGGCCTGTGTGCTGCCGGATTCCCTGCCTCCATCACCCGACCGCCACTC A G CEP68 Ensembl:ENSG00000011523 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:65071883..65071998 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_774452,Human_RBP_ID_8523249,Human_RBP_ID_27481180 RMVar_hsa_circ_50680,RMVar_hsa_circ_115302,RMVar_hsa_circ_377319,RMVar_hsa_circ_200772,RMVar_hsa_circ_315665,RMVar_hsa_circ_200773 114190 RMVar_ID_114190 Human_SNP_ID_834829088 m1A Human chr2 - 215397188 215397188 215397188 TGTCTCCACCAACAAACTTGCATCTGGAGGCAAACCCTGACACTGGAGTGCTCACAGTCTCCTGG TGTCTCCACCAACAAACTTGCATCTGGAGGCAGACCCTGACACTGGAGTGCTCACAGTCTCCTGG T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215394541..215399272 32194978 MeRIP-seq:(Medium) rs746992481 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 12 liver Human_RBP_ID_142813,Human_RBP_ID_775175,Human_RBP_ID_829302,Human_RBP_ID_921731,Human_RBP_ID_5239710,Human_RBP_ID_17279313,Human_RBP_ID_17698346,Human_RBP_ID_17965699,Human_RBP_ID_22450725,Human_RBP_ID_22765242 Human_Splice_Rec_355070,Human_Splice_Rec_355071,Human_Splice_Rec_355158,Human_Splice_Rec_355159,Human_Splice_Rec_355248,Human_Splice_Rec_355249,Human_Splice_Rec_355340,Human_Splice_Rec_355341,Human_Splice_Rec_355430,Human_Splice_Rec_355431,Human_Splice_Rec_355516,Human_Splice_Rec_355517,Human_Splice_Rec_355640,Human_Splice_Rec_355641,Human_Splice_Rec_355730,Human_Splice_Rec_355731,Human_Splice_Rec_355818,Human_Splice_Rec_355819,Human_Splice_Rec_355908,Human_Splice_Rec_355909 Human_miRNA_ID_2174461,Human_miRNA_ID_2174462,Human_miRNA_ID_2177905,Human_miRNA_ID_2177906 RMVar_hsa_circ_23898,RMVar_hsa_circ_3650,RMVar_hsa_circ_102121,RMVar_hsa_circ_101661,RMVar_hsa_circ_206712,RMVar_hsa_circ_109669,RMVar_hsa_circ_206714,RMVar_hsa_circ_84870,RMVar_hsa_circ_206716,RMVar_hsa_circ_206717,RMVar_hsa_circ_63624,RMVar_hsa_circ_79478,RMVar_hsa_circ_265376,RMVar_hsa_circ_122684,RMVar_hsa_circ_88845,RMVar_hsa_circ_206721,RMVar_hsa_circ_206722,RMVar_hsa_circ_206723,RMVar_hsa_circ_53921,RMVar_hsa_circ_81432,RMVar_hsa_circ_206727,RMVar_hsa_circ_380,RMVar_hsa_circ_120836,RMVar_hsa_circ_93135,RMVar_hsa_circ_121202,RMVar_hsa_circ_206728,RMVar_hsa_circ_206729,RMVar_hsa_circ_123745,RMVar_hsa_circ_113512,RMVar_hsa_circ_23850,RMVar_hsa_circ_206733,RMVar_hsa_circ_206734,RMVar_hsa_circ_206735,RMVar_hsa_circ_37635,RMVar_hsa_circ_112126,RMVar_hsa_circ_56306,RMVar_hsa_circ_206738,RMVar_hsa_circ_45854,RMVar_hsa_circ_51496,RMVar_hsa_circ_30025,RMVar_hsa_circ_110836,RMVar_hsa_circ_39583,RMVar_hsa_circ_101080,RMVar_hsa_circ_268941,RMVar_hsa_circ_206741,RMVar_hsa_circ_269134,RMVar_hsa_circ_266791,RMVar_hsa_circ_206742,RMVar_hsa_circ_100587,RMVar_hsa_circ_116298,RMVar_hsa_circ_206744,RMVar_hsa_circ_64680,RMVar_hsa_circ_206745,RMVar_hsa_circ_61971,RMVar_hsa_circ_375535,RMVar_hsa_circ_63479,RMVar_hsa_circ_358981,RMVar_hsa_circ_117625,RMVar_hsa_circ_206747,RMVar_hsa_circ_206748,RMVar_hsa_circ_370112,RMVar_hsa_circ_330683,RMVar_hsa_circ_206750,RMVar_hsa_circ_66168,RMVar_hsa_circ_85394,RMVar_hsa_circ_64362,RMVar_hsa_circ_206751,RMVar_hsa_circ_53859 114191 RMVar_ID_114191 Human_SNP_ID_834871819 m1A Human chr2 + 218275439 218275439 218275439 GTCATAGGGCCCAGCCCTCTAGCTTGGAAGGGAGAGCCCAGGATCGGGTGAAAATGGGGGCTTGC GTCATAGGGCCCAGCCCTCTAGCTTGGAAGGGGGAGCCCAGGATCGGGTGAAAATGGGGGCTTGC A G PNKD Ensembl:ENSG00000127838 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218275390..218275491 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 114192 RMVar_ID_114192 Human_SNP_ID_834882670 m1A Human chr2 - 3314755 3314755 3314755 GTCCTGGGGAGAGGCTAGCTGGAGGCTGGGGGAGAGAGCTTTCTGCAGGCAGTCAGAGGGGCATC GTCCTGGGGAGAGGCTAGCTGGAGGCTGGGGGGGAGAGCTTTCTGCAGGCAGTCAGAGGGGCATC T C EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3314751..3315174 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3637824,Human_RBP_ID_8109717,Human_RBP_ID_8200275,Human_RBP_ID_8234620,Human_RBP_ID_8942546,Human_RBP_ID_9429146,Human_RBP_ID_23282591 RMVar_hsa_circ_77820,RMVar_hsa_circ_196687,RMVar_hsa_circ_82748,RMVar_hsa_circ_196689,RMVar_hsa_circ_337810,RMVar_hsa_circ_319957,RMVar_hsa_circ_196690 114193 RMVar_ID_114193 Human_SNP_ID_834886991 m1A Human chr2 - 85596883 85596878 85596883 AGAATGCAGCTGGAATGGAAAAGGTGATGGCAAGGCATCTCAATGGCAGTCTCCTCCTCCTCAAA AGAATGCAGCTGGAATGGAAAAGGTGATGGCA_____TCTCAATGGCAGTCTCCTCCTCCTCAAA ATGCCT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:85596801..85596950;chr2:85596797..85596930 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..37 33 HNSC 1 - 114194 RMVar_ID_114194 Human_SNP_ID_834952238 m1A Human chr2 - 63622383 63622383 63622383 CTCCAGAGCTGTCCAGGAATTTGGTCTTGCCCAGTTCAAAAGCAACGTGACCAAGACTATGAAGG CTCCAGAGCTGTCCAGGAATTTGGTCTTGCCCGGTTCAAAAGCAACGTGACCAAGACTATGAAGG T C WDPCP,AC016734.1 Ensembl:ENSG00000143951,Ensembl:ENSG00000228305 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs878899773 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA,LAML 3 - Human_miRNA_ID_1853028 114195 RMVar_ID_114195 Human_SNP_ID_834954103 m1A Human chr2 - 96208715 96208715 96208715 TCCCGGCCCCGGGCGCCCGCTGGAGGTCGCCGAGGAGCCACAGGGCTGACTGGTCTGCTGCCCGG TCCCGGCCCCGGGCGCCCGCTGGAGGTCGCCGCGGAGCCACAGGGCTGACTGGTCTGCTGCCCGG T G STARD7 Ensembl:ENSG00000084090 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:96208615..96208825 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_777918,Human_RBP_ID_4622544,Human_RBP_ID_5322523,Human_RBP_ID_5471426,Human_RBP_ID_5527877,Human_RBP_ID_8851395,Human_RBP_ID_9296669,Human_RBP_ID_9330558,Human_RBP_ID_22076456,Human_RBP_ID_22451497 114196 RMVar_ID_114196 Human_SNP_ID_834991183 m1A Human chr2 - 47029237 47029237 47029237 TGCGTACCTTCAGGGCCTCCTGCAGCTGCTCCATGGCACTGGAGATCTGTTGAAGGAACCCGCCA TGCGTACCTTCAGGGCCTCCTGCAGCTGCTCCCTGGCACTGGAGATCTGTTGAAGGAACCCGCCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:47023413..47029249 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 114197 RMVar_ID_114197 Human_SNP_ID_835009837 m1A Human chr2 + 73225894 73225891 73225895 CTCAGAAGAGGAAGAGGAAGAGGAGGAGGAGGAGGAAGGAGAGCCAGAAGATGCAGAGCTGGGGG CTCAGAAGAGGAAGAGGAAGAGGAGGAGGA____GAAGGAGAGCCAGAAGATGCAGAGCTGGGGG AGGAG A SMYD5 Ensembl:ENSG00000135632 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:73225844..73225994 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..34 33 STAD 1 - Human_RBP_ID_4615900,Human_RBP_ID_5527735,Human_RBP_ID_19001832,Human_RBP_ID_22451365,Human_RBP_ID_27481622 Human_Splice_Rec_262120,Human_Splice_Rec_262152 Human_miRNA_ID_336858,Human_miRNA_ID_2082356 RMVar_hsa_circ_113656,RMVar_hsa_circ_91711,RMVar_hsa_circ_201202,RMVar_hsa_circ_119720,RMVar_hsa_circ_201203,RMVar_hsa_circ_201205 114198 RMVar_ID_114198 Human_SNP_ID_835018923 m1A Human chr2 - 241676176 241676176 241676176 TGTCCATGAGGACATCCGCGTGCTCTCTGAGGACGCCATCCGCACTGCCACAGAGAAGCCGCTGG TGTCCATGAGGACATCCGCGTGCTCTCTGAGGGCGCCATCCGCACTGCCACAGAGAAGCCGCTGG T C DTYMK Ensembl:ENSG00000168393 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241676151..241676175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_547379,Human_RBP_ID_1022654,Human_RBP_ID_1300335,Human_RBP_ID_1585140,Human_RBP_ID_4603084,Human_RBP_ID_8515855,Human_RBP_ID_17658299,Human_RBP_ID_22076927,Human_RBP_ID_27288545 Human_Splice_Rec_383256,Human_Splice_Rec_383262,Human_Splice_Rec_383270,Human_Splice_Rec_383278,Human_Splice_Rec_383286 RMVar_hsa_circ_94187,RMVar_hsa_circ_208207 114199 RMVar_ID_114199 Human_SNP_ID_835024760 m1A Human chr2 - 241150549 241150549 241150549 GGCCCTTGGGCCGCCGCCCGCAGGGGCCGCTCACCCTCCATCATCTCCTGCGACTGTTGCTGCCC GGCCCTTGGGCCGCCGCCCGCAGGGGCCGCTCGCCCTCCATCATCTCCTGCGACTGTTGCTGCCC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr2:241150476..241150649;chr2:241150541..241150668;chr2:241150476..241150575 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach 114200 RMVar_ID_114200 Human_SNP_ID_835035087 m1A Human chr2 - 203043679 203043679 203043679 TGTCACCCAGGCTGGAGTGCAGTGGCACGATCACAGCACACTACAGCCTCAACTCTCTGGGCCAA TGTCACCCAGGCTGGAGTGCAGTGGCACGATCGCAGCACACTACAGCCTCAACTCTCTGGGCCAA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203043677..203043806 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114201 RMVar_ID_114201 Human_SNP_ID_835048606 m1A Human chr2 + 74369447 74369447 74369447 TCCAGCTGCTCCCGCAGCTCCAGTTCTGTCTCACGTGCATTCTCCTGCAGCTCATCGTTCATCTC TCCAGCTGCTCCCGCAGCTCCAGTTCTGTCTCGCGTGCATTCTCCTGCAGCTCATCGTTCATCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74369311..74369534 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114202 RMVar_ID_114202 Human_SNP_ID_835073561 m1A Human chr2 + 235822567 235822567 235822567 GCTGAAGAAGCTCAAGGGTGAGGAGGAGCTGGAGAAGCCCAAGGGTGAAGAGAAGCTGGAGAAGC GCTGAAGAAGCTCAAGGGTGAGGAGGAGCTGGGGAAGCCCAAGGGTGAAGAGAAGCTGGAGAAGC A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:235822318..235822815 26863196 MeRIP-seq:(Medium) rs1298857387 Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_22597325 RMVar_hsa_circ_330369,RMVar_hsa_circ_44106,RMVar_hsa_circ_207763,RMVar_hsa_circ_91320,RMVar_hsa_circ_17639,RMVar_hsa_circ_207768,RMVar_hsa_circ_344448,RMVar_hsa_circ_60410,RMVar_hsa_circ_7507,RMVar_hsa_circ_84214,RMVar_hsa_circ_207772,RMVar_hsa_circ_332313,RMVar_hsa_circ_370048,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_332938,RMVar_hsa_circ_207773,RMVar_hsa_circ_323537,RMVar_hsa_circ_207782 114203 RMVar_ID_114203 Human_SNP_ID_835098304 m1A Human chr2 + 225582684 225582684 225582684 CGTCGCCCCCACCCCCGTCTACGCTGTACCGAACCCAGTCTCCCCATGGCTACCCTAAAAGTCAC CGTCGCCCCCACCCCCGTCTACGCTGTACCGAGCCCAGTCTCCCCATGGCTACCCTAAAAGTCAC A G NYAP2 Ensembl:ENSG00000144460 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225582339..225582750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach RMVar_hsa_circ_310845,RMVar_hsa_circ_207304 114204 RMVar_ID_114204 Human_SNP_ID_835116791 m1A Human chr2 - 171160441 171160441 171160441 CGCTGCCGTCGCAGGGGGGGAGTCGGGTTCCCAGAAAGTAGCTTGATGAGTGTCCAAAGTAGCAG CGCTGCCGTCGCAGGGGGGGAGTCGGGTTCCCGGAAAGTAGCTTGATGAGTGTCCAAAGTAGCAG T C TLK1 Ensembl:ENSG00000198586 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:171160268..171231165;chr2:171160245..171231165 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_3638207,Human_RBP_ID_4628154,Human_RBP_ID_5131661,Human_RBP_ID_9429369,Human_RBP_ID_17084674,Human_RBP_ID_17569335,Human_RBP_ID_18442683,Human_RBP_ID_18462233,Human_RBP_ID_18493626,Human_RBP_ID_18949672 RMVar_hsa_circ_127131,RMVar_hsa_circ_204598,RMVar_hsa_circ_118263,RMVar_hsa_circ_204606,RMVar_hsa_circ_125471,RMVar_hsa_circ_204610 114205 RMVar_ID_114205 Human_SNP_ID_835126231 m1A Human chr2 - 1656920 1656920 1656920 GGCAGGAGGGGACAGGTTTCTGTCAGGAGGGGACAGGTTCCAGTCAGGAGGGGGTAGGTCCCTGT GGCAGGAGGGGACAGGTTTCTGTCAGGAGGGGGCAGGTTCCAGTCAGGAGGGGGTAGGTCCCTGT T C PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1656918..1657004 26863196 MeRIP-seq:(Medium) rs1158525373 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 114206 RMVar_ID_114206 Human_SNP_ID_835149822 m1A Human chr2 + 210599474 210599474 210599474 AGCAAGCGGATACTGTCTACTTTCTTCCCATCACCCCTCAGTTTGTCACAGAGGTCATCAAGGCA AGCAAGCGGATACTGTCTACTTTCTTCCCATCTCCCCTCAGTTTGTCACAGAGGTCATCAAGGCA A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:210599423..210599499 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 5 bladder,urinary tract Human_RBP_ID_2619998,Human_RBP_ID_24488005,Human_RBP_ID_27477421 Human_Splice_Rec_353109,Human_Splice_Rec_353187,Human_Splice_Rec_353263,Human_Splice_Rec_353339,Human_Splice_Rec_353413,Human_Splice_Rec_353495,Human_Splice_Rec_353549,Human_Splice_Rec_353597 Human_miRNA_ID_2152870,Human_miRNA_ID_2800746,Human_miRNA_ID_3008875 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_21428,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_72435,RMVar_hsa_circ_69514,RMVar_hsa_circ_100412,RMVar_hsa_circ_70074,RMVar_hsa_circ_55652,RMVar_hsa_circ_73167,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_60939,RMVar_hsa_circ_69154,RMVar_hsa_circ_69776,RMVar_hsa_circ_80365,RMVar_hsa_circ_58119,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_74078,RMVar_hsa_circ_73146,RMVar_hsa_circ_24212,RMVar_hsa_circ_58944,RMVar_hsa_circ_86182,RMVar_hsa_circ_102148,RMVar_hsa_circ_75386,RMVar_hsa_circ_206570,RMVar_hsa_circ_206571 114207 RMVar_ID_114207 Human_SNP_ID_835169033 m1A Human chr2 + 159748854 159748854 159748854 GGAATTCAGCTGATGGTAAAAGTGATAAAACTAAAAGTGCGCCTTCAAGAGATCCAGAAAGATTG GGAATTCAGCTGATGGTAAAAGTGATAAAACTTAAAGTGCGCCTTCAAGAGATCCAGAAAGATTG A T MARCHF7 Ensembl:ENSG00000136536 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:159748671..159752420 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_1901157,Human_RBP_ID_8843219,Human_RBP_ID_22077759,Human_RBP_ID_23833081,Human_RBP_ID_27688054 Human_Splice_Rec_312573,Human_Splice_Rec_312589,Human_Splice_Rec_312611,Human_Splice_Rec_312639 Human_miRNA_ID_2854326,Human_miRNA_ID_2857006 RMVar_hsa_circ_99514,RMVar_hsa_circ_366916,RMVar_hsa_circ_204090,RMVar_hsa_circ_65907,RMVar_hsa_circ_204097,RMVar_hsa_circ_66716,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094,RMVar_hsa_circ_204099,RMVar_hsa_circ_46050,RMVar_hsa_circ_204098,RMVar_hsa_circ_102455,RMVar_hsa_circ_312558,RMVar_hsa_circ_329688,RMVar_hsa_circ_272313,RMVar_hsa_circ_204101,RMVar_hsa_circ_204100,RMVar_hsa_circ_204108,RMVar_hsa_circ_204106,RMVar_hsa_circ_300894,RMVar_hsa_circ_270484,RMVar_hsa_circ_204105,RMVar_hsa_circ_204110,RMVar_hsa_circ_297092,RMVar_hsa_circ_319976,RMVar_hsa_circ_356041,RMVar_hsa_circ_310061,RMVar_hsa_circ_118630,RMVar_hsa_circ_204109,RMVar_hsa_circ_204107,RMVar_hsa_circ_204111 114208 RMVar_ID_114208 Human_SNP_ID_835174886 m1A Human chr2 - 231460703 231460703 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGATGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs199689485 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,colon adenocarcinoma,rectum adenocarcinoma,large_intestine adenocarcinoma 4 kidney,large intestine Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 114209 RMVar_ID_114209 Human_SNP_ID_835176041 m1A Human chr2 - 237085966 237085951 237085966 TAAAGGCGCTTTCCGCCATCACCGCCACTGGCATCTTCGCGGCCGGCCTCGCCGCTGCACCGTCC TAAAGGCGCTTTCCGCCATCACCGCCACTGGC_______________CTCGCCGCTGCACCGTCC GGCCGGCCGCGAAGAT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr2:237085901..237086050;chr2:237085926..237086077;chr2:237085901..237086148;chr2:237085901..237086044 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..47 33 BRCA 1 - 114210 RMVar_ID_114210 Human_SNP_ID_835179013 m1A Human chr2 - 38377198 38377198 38377198 CAGCAACCGCACCAGGGGCTGTGGCGCCGGCGACGGACCAGCGACCCAAGCGCCGCGGTTAACCA CAGCAACCGCACCAGGGGCTGTGGCGCCGGCGCCGGACCAGCGACCCAAGCGCCGCGGTTAACCA T G ATL2 Ensembl:ENSG00000119787 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:38377142..38377237 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_4608893,Human_RBP_ID_18421742,Human_RBP_ID_22449779,Human_RBP_ID_22996802,Human_RBP_ID_27840013 Human_Splice_Rec_236755,Human_Splice_Rec_236779,Human_Splice_Rec_236825,Human_Splice_Rec_236847,Human_Splice_Rec_236871,Human_Splice_Rec_236945,Human_Splice_Rec_236953,Human_Splice_Rec_236965,Human_Splice_Rec_236979,Human_Splice_Rec_236983,Human_Splice_Rec_236993 114211 RMVar_ID_114211 Human_SNP_ID_835189109 m1A Human chr2 - 189771751 189771751 189771751 GAATTAATAAGTATTGAAATGTTTTGAAACTGAAAAAAAATTTTACAGCTACTGAATTTCTTATA GAATTAATAAGTATTGAAATGTTTTGAAACTGGAAAAAAATTTTACAGCTACTGAATTTCTTATA T C ORMDL1 Ensembl:ENSG00000128699 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1429105605 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_540514,Human_RBP_ID_1905874,Human_RBP_ID_9099670,Human_RBP_ID_22998344,Human_RBP_ID_23843918 114212 RMVar_ID_114212 Human_SNP_ID_835197204 m1A Human chr2 + 47791001 47791001 47791001 GGGTTACCCCTGGTGGCCTTGTCTGGTTTACAACCACCCCTTTGATGGAACATTCATCCGCGAGA GGGTTACCCCTGGTGGCCTTGTCTGGTTTACAGCCACCCCTTTGATGGAACATTCATCCGCGAGA A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:47790976..47791000 26863196 MeRIP-seq:(Medium) rs587779934 Functional Loss SNV TCGA 33..33 33 UCS 1 - Human_RBP_ID_1587527,Human_RBP_ID_6927772,Human_RBP_ID_8848550,Human_RBP_ID_9296475,Human_RBP_ID_22450300,Human_RBP_ID_22815722 Human_Splice_Rec_243300,Human_Splice_Rec_243318,Human_Splice_Rec_243334,Human_Splice_Rec_243350,Human_Splice_Rec_243372,Human_Splice_Rec_243390,Human_Splice_Rec_243396,Human_Splice_Rec_243430,Human_Splice_Rec_243436,Human_Splice_Rec_243440,Human_Splice_Rec_243458 Clinvar_Rec_722,Clinvar_Rec_723 RMVar_hsa_circ_59777,RMVar_hsa_circ_84947,RMVar_hsa_circ_318360,RMVar_hsa_circ_356073,RMVar_hsa_circ_199625,RMVar_hsa_circ_328509,RMVar_hsa_circ_296979,RMVar_hsa_circ_199626,RMVar_hsa_circ_199627,RMVar_hsa_circ_199628 114213 RMVar_ID_114213 Human_SNP_ID_835222934 m1A Human chr2 + 28776858 28776858 28776858 GACTGTTTTATTTATCGTTTGTCAGTACGAGGATGTCGTCCAGGAAAGATTGTGCAGATGACTGA GACTGTTTTATTTATCGTTTGTCAGTACGAGGGTGTCGTCCAGGAAAGATTGTGCAGATGACTGA A G PPP1CB Ensembl:ENSG00000213639 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:28776851..28776900 26863196 MeRIP-seq:(Medium) rs775116467 Functional Loss SNV ICGC 33..33 33 NKTL 1 - Human_RBP_ID_829390,Human_RBP_ID_915406,Human_RBP_ID_1585800,Human_RBP_ID_2636010,Human_RBP_ID_4606437,Human_RBP_ID_8234273,Human_RBP_ID_8516994,Human_RBP_ID_8851817,Human_RBP_ID_9259677,Human_RBP_ID_9296408,Human_RBP_ID_13849659,Human_RBP_ID_22452131,Human_RBP_ID_22667153,Human_RBP_ID_23866240,Human_RBP_ID_24377144 Human_Splice_Rec_230934,Human_Splice_Rec_230944,Human_Splice_Rec_230950,Human_Splice_Rec_230954,Human_Splice_Rec_230962,Human_Splice_Rec_230978,Human_Splice_Rec_230992,Human_Splice_Rec_231006 Human_miRNA_ID_2508574 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_270896,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273853,RMVar_hsa_circ_330912,RMVar_hsa_circ_361161,RMVar_hsa_circ_319196,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_198110,RMVar_hsa_circ_198111,RMVar_hsa_circ_198109 114214 RMVar_ID_114214 Human_SNP_ID_835246567 m1A Human chr2 - 74215015 74215014 74215015 AAGATACACCAAAGAAACTATACAATACAAAAATTTAACAATGAAGTTAAAGTATATAGCAAAAG AAGATACACCAAAGAAACTATACAATACAAAA_TTTAACAATGAAGTTAAAGTATATAGCAAAAG AT A AC006030.1 Ensembl:ENSG00000264324 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74214931..74215031 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 114215 RMVar_ID_114215 Human_SNP_ID_835284581 m1A Human chr2 + 56384346 56384346 56384346 AGGCAACATTTGTCAGGAAACCAGTACAAAGGACCAATGTGAGATGCACTCTTTTTCAAACAGGA AGGCAACATTTGTCAGGAAACCAGTACAAAGGTCCAATGTGAGATGCACTCTTTTTCAAACAGGA A T AC007744.1,CCDC85A Ensembl:ENSG00000271894,Ensembl:ENSG00000055813 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:56342920..56384380 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_Splice_Rec_249116,Human_Splice_Rec_249152 RMVar_hsa_circ_266112 114216 RMVar_ID_114216 Human_SNP_ID_835285133 m1A Human chr2 + 74198651 74198651 74198651 CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGACTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG CGGCGCAGTCACCGGCGCGGTCTATGGCTGCGGCTTCTCTAATGTCTGCTTTGGCTGCCCGGCTG A G MTHFD2 Ensembl:ENSG00000065911 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74198601..74198700 26863196 MeRIP-seq:(Medium) rs780949855 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_555681,Human_RBP_ID_774551,Human_RBP_ID_1024185,Human_RBP_ID_1590349,Human_RBP_ID_4616648,Human_RBP_ID_5275734,Human_RBP_ID_5423276,Human_RBP_ID_5445121,Human_RBP_ID_5502587,Human_RBP_ID_6950144,Human_RBP_ID_8109289,Human_RBP_ID_8525412,Human_RBP_ID_8849923,Human_RBP_ID_9330524,Human_RBP_ID_13965287,Human_RBP_ID_17392714,Human_RBP_ID_18765751,Human_RBP_ID_23885497,Human_RBP_ID_26818613,Human_RBP_ID_27698494 Human_Splice_Rec_263297,Human_Splice_Rec_263305,Human_Splice_Rec_263317,Human_Splice_Rec_263325,Human_Splice_Rec_263335,Human_Splice_Rec_263349,Human_Splice_Rec_263359 RMVar_hsa_circ_84324,RMVar_hsa_circ_201296 114217 RMVar_ID_114217 Human_SNP_ID_835318249 m1A Human chr2 - 23422533 23422533 23422533 CACAGGCACACAACACAGAGAGACACAGACACATGGACACACACAGAGACACACATAACACACAG CACAGGCACACAACACAGAGAGACACAGACACGTGGACACACACAGAGACACACATAACACACAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:23422515..23422729 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114218 RMVar_ID_114218 Human_SNP_ID_835333481 m1A Human chr2 - 70248549 70248549 70248549 TTTAGTGTAATTGCCGCCGGAGGAGGAGGCGGAGTAACCTCTGGTCAGCCGAGAAACCCCACTAT TTTAGTGTAATTGCCGCCGGAGGAGGAGGCGGGGTAACCTCTGGTCAGCCGAGAAACCCCACTAT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding 5'UTR,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:70248401..70248668;chr2:70248401..70248669 26863196 MeRIP-seq:(Medium) rs1328821263 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_242629,Human_RBP_ID_775397,Human_RBP_ID_830696,Human_RBP_ID_915530,Human_RBP_ID_4623375,Human_RBP_ID_8524206,Human_RBP_ID_9330503,Human_RBP_ID_9383974,Human_RBP_ID_13950475,Human_RBP_ID_18421817,Human_RBP_ID_26339400,Human_RBP_ID_27817211 RMVar_hsa_circ_201028,RMVar_hsa_circ_125086 114219 RMVar_ID_114219 Human_SNP_ID_835336186 m1A Human chr2 - 27071465 27071465 27071465 CCAGCCCGCAGCTCAGCCCCTCTCTTCTCCGCAGGATGATCACGGACGTGCAGCTCGCCATCTTC CCAGCCCGCAGCTCAGCCCCTCTCTTCTCCGCCGGATGATCACGGACGTGCAGCTCGCCATCTTC T G OST4 Ensembl:ENSG00000228474 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:27071376..27071587 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_917684,Human_RBP_ID_19099598 RMVar_hsa_circ_197877 114220 RMVar_ID_114220 Human_SNP_ID_835338810 m1A Human chr2 + 159230181 159230181 159230181 GCTGGGAGCAGAACCCAGCATTTAGAGGGAACAGGTACTTTCACTACAAGAGCTGGTTGTGGCCA GCTGGGAGCAGAACCCAGCATTTAGAGGGAACGGGTACTTTCACTACAAGAGCTGGTTGTGGCCA A G TANC1 Ensembl:ENSG00000115183 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3821296 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 large intestine,haematopoietic and lymphoid tissue Human_miRNA_ID_1978493,Human_miRNA_ID_1978494,Human_miRNA_ID_2958627,Human_miRNA_ID_2958628 GWAS_ID_7462,GWAS_ID_7463,GWAS_ID_7464,GWAS_ID_7465,GWAS_ID_7466 RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_89610,RMVar_hsa_circ_204040,RMVar_hsa_circ_204041 114221 RMVar_ID_114221 Human_SNP_ID_835347456 m1A Human chr2 + 219493270 219493270 219493270 CACAGATACAGTGGCAGGGGCCCAGGGCTGGGACATGAGAGAAGGCAGCGAGGCGGCAGAGGGAG CACAGATACAGTGGCAGGGGCCCAGGGCTGGGTCATGAGAGAAGGCAGCGAGGCGGCAGAGGGAG A T AC053503.6,SPEG Ensembl:ENSG00000286143,Ensembl:ENSG00000072195 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:219493133..219493309 26863196 MeRIP-seq:(Medium) rs377226202 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain 114222 RMVar_ID_114222 Human_SNP_ID_835361352 m1A Human chr2 + 101858932 101858932 101858932 AGGTGATTGGAGCAAATGGTTCTTGGTGCTCCATTCAGGTGGTTCTGATGCTTTTCTTTGGGATA AGGTGATTGGAGCAAATGGTTCTTGGTGCTCCGTTCAGGTGGTTCTGATGCTTTTCTTTGGGATA A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:101858929..101859100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_3582,RMVar_hsa_circ_70658,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_116064,RMVar_hsa_circ_202264,RMVar_hsa_circ_21524,RMVar_hsa_circ_315560,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_342280,RMVar_hsa_circ_53472,RMVar_hsa_circ_202265 114223 RMVar_ID_114223 Human_SNP_ID_835388051 m1A Human chr2 - 10790809 10790809 10790809 TTCTATAGCCTAGAGCCAGAGTGGGCTGCCGCAGCTTCAGAAGTAAAAGAGCAGACGAAAGGAAA TTCTATAGCCTAGAGCCAGAGTGGGCTGCCGCCGCTTCAGAAGTAAAAGAGCAGACGAAAGGAAA T G PDIA6 Ensembl:ENSG00000143870 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:10789726..10790809 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_531724,Human_RBP_ID_775978,Human_RBP_ID_829778,Human_RBP_ID_922733,Human_RBP_ID_1576669,Human_RBP_ID_2577512,Human_RBP_ID_6812198,Human_RBP_ID_9259621,Human_RBP_ID_9383105,Human_RBP_ID_17699940,Human_RBP_ID_17965823,Human_RBP_ID_22449713,Human_RBP_ID_22764887,Human_RBP_ID_23817458,Human_RBP_ID_26338968 Human_Splice_Rec_217926,Human_Splice_Rec_217927,Human_Splice_Rec_217952,Human_Splice_Rec_217953,Human_Splice_Rec_217978,Human_Splice_Rec_217979,Human_Splice_Rec_218006,Human_Splice_Rec_218007,Human_Splice_Rec_218032,Human_Splice_Rec_218033,Human_Splice_Rec_218058,Human_Splice_Rec_218059 RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303,RMVar_hsa_circ_314125,RMVar_hsa_circ_336161,RMVar_hsa_circ_379037,RMVar_hsa_circ_290480,RMVar_hsa_circ_196999,RMVar_hsa_circ_315097,RMVar_hsa_circ_297066,RMVar_hsa_circ_196998,RMVar_hsa_circ_267370,RMVar_hsa_circ_316864,RMVar_hsa_circ_364625 114224 RMVar_ID_114224 Human_SNP_ID_835389855 m1A Human chr2 + 218993096 218993096 218993096 TCGCAGACGTTCGCACAGTCGCTTAGCAGCCGACAGCGACGGCCCTGGAAGTCCTCCTCGTCCCA TCGCAGACGTTCGCACAGTCGCTTAGCAGCCGGCAGCGACGGCCCTGGAAGTCCTCCTCGTCCCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218993059..218993126 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 114225 RMVar_ID_114225 Human_SNP_ID_835431163 m1A Human chr2 - 72825962 72825962 72825962 GCCTGTGGTGGGAGCGGCATTGTGGGGCAGGGAAAAGGTGAGCCGAGCCGACGGAGGGGACGCGC GCCTGTGGTGGGAGCGGCATTGTGGGGCAGGGGAAAGGTGAGCCGAGCCGACGGAGGGGACGCGC T C EXOC6B Ensembl:ENSG00000144036 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:72825776..72826025;chr2:72741384..72826050;chr2:72741412..72826050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_5528605,Human_RBP_ID_9386826,Human_RBP_ID_18422248,Human_RBP_ID_27817253 RMVar_hsa_circ_116271,RMVar_hsa_circ_201171,RMVar_hsa_circ_85215,RMVar_hsa_circ_201173 114226 RMVar_ID_114226 Human_SNP_ID_835431165 m1A Human chr2 - 72825962 72825962 72825962 GCCTGTGGTGGGAGCGGCATTGTGGGGCAGGGAAAAGGTGAGCCGAGCCGACGGAGGGGACGCGC GCCTGTGGTGGGAGCGGCATTGTGGGGCAGGGTAAAGGTGAGCCGAGCCGACGGAGGGGACGCGC T A EXOC6B Ensembl:ENSG00000144036 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:72825776..72826025;chr2:72741384..72826050;chr2:72741412..72826050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_5528605,Human_RBP_ID_9386826,Human_RBP_ID_18422248,Human_RBP_ID_27817253 RMVar_hsa_circ_116271,RMVar_hsa_circ_201171,RMVar_hsa_circ_85215,RMVar_hsa_circ_201173 114227 RMVar_ID_114227 Human_SNP_ID_835472273 m1A Human chr2 + 169810985 169810985 169810985 TTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGAAGCACTGAAGAAAATAATAGAAGACCAACAAG TTGGGAAGTACTAGAAGGAGAGGTGGAAAAAGCAGCACTGAAGAAAATAATAGAAGACCAACAAG A C SSB Ensembl:ENSG00000138385 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:169810877..169811026 26863196 MeRIP-seq:(Medium) rs777853278 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney Human_RBP_ID_205441,Human_RBP_ID_242869,Human_RBP_ID_829486,Human_RBP_ID_922050,Human_RBP_ID_1902066,Human_RBP_ID_3602955,Human_RBP_ID_5588756,Human_RBP_ID_6847538,Human_RBP_ID_8234702,Human_RBP_ID_8257354,Human_RBP_ID_9385055,Human_RBP_ID_18515456,Human_RBP_ID_18533365,Human_RBP_ID_24545902,Human_RBP_ID_26340060,Human_RBP_ID_27817746 Human_Splice_Rec_320593,Human_Splice_Rec_320639 Human_miRNA_ID_2842574 RMVar_hsa_circ_82825,RMVar_hsa_circ_204471,RMVar_hsa_circ_376954 114228 RMVar_ID_114228 Human_SNP_ID_835478241 m1A Human chr2 + 218959888 218959888 218959888 GGCCAAGGGCCGGAGGCCCGGCGGGCTGCCCGAGGAGAAGAAGAAGGCGCCGCCCGCGGGGGACG GGCCAAGGGCCGGAGGCCCGGCGGGCTGCCCGTGGAGAAGAAGAAGGCGCCGCCCGCGGGGGACG A T CDK5R2 Ensembl:ENSG00000171450 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:218959850..218959973 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114229 RMVar_ID_114229 Human_SNP_ID_835484792 m1A Human chr2 + 10190581 10190581 10190581 TGAGGATGGTGGTGGTGATGATGGTGATGATCATGGTGATGGTGGTGATGTTGGCGATGATGGTG TGAGGATGGTGGTGGTGATGATGGTGATGATCTTGGTGATGGTGGTGATGTTGGCGATGATGGTG A T RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:10189908..10190627 26863196 MeRIP-seq:(Medium) rs111163325 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5651826,Human_RBP_ID_8110132,Human_RBP_ID_22743167 114230 RMVar_ID_114230 Human_SNP_ID_835487673 m1A Human chr2 + 197310635 197310635 197310635 ATTCTTCCGCTCCTTCGCGCGCACACACATGCAGGTCCCCGGCCCGCAGATGTCACGCCGGGAGC ATTCTTCCGCTCCTTCGCGCGCACACACATGCGGGTCCCCGGCCCGCAGATGTCACGCCGGGAGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:197310584..197310808 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 5 kidney 114231 RMVar_ID_114231 Human_SNP_ID_835488003 m1A Human chr2 - 203440400 203440400 203440400 CCTCCTGAAAGCAGCCTGGTGTTTCCTCCTCCACCCCCATCACCTGTCCCAGCCCCACCACCACC CCTCCTGAAAGCAGCCTGGTGTTTCCTCCTCCCCCCCCATCACCTGTCCCAGCCCCACCACCACC T G RAPH1 Ensembl:ENSG00000173166 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:203440351..203440700 26863196 MeRIP-seq:(Medium) rs1425961684 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_3638978,Human_RBP_ID_5131677,Human_RBP_ID_17085514,Human_RBP_ID_18948485,Human_RBP_ID_27483060 Human_miRNA_ID_1358748 114232 RMVar_ID_114232 Human_SNP_ID_835492089 m1A Human chr2 - 95108264 95108264 95108264 GATCCAGCAGAGAGAAGAGTGGGACCGAAAGAAGAAGATGAAGGTTAAACGGGAGCGAGGATGGA GATCCAGCAGAGAGAAGAGTGGGACCGAAAGAGGAAGATGAAGGTTAAACGGGAGCGAGGATGGA T C MRPS5 Ensembl:ENSG00000144029 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:95106601..95110084;chr2:95106582..95110025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_8811,Human_RBP_ID_828505,Human_RBP_ID_1592334,Human_RBP_ID_6957459,Human_RBP_ID_8234411,Human_RBP_ID_9384220,Human_RBP_ID_18412764,Human_RBP_ID_22997399,Human_RBP_ID_24545810,Human_RBP_ID_26338626,Human_RBP_ID_27817317 Human_Splice_Rec_273235,Human_Splice_Rec_273259,Human_Splice_Rec_273297 Human_miRNA_ID_2194431,Human_miRNA_ID_2891642 RMVar_hsa_circ_27338,RMVar_hsa_circ_88336,RMVar_hsa_circ_119653,RMVar_hsa_circ_201780,RMVar_hsa_circ_201781,RMVar_hsa_circ_341041,RMVar_hsa_circ_65050,RMVar_hsa_circ_127801,RMVar_hsa_circ_201785 114233 RMVar_ID_114233 Human_SNP_ID_835550162 m1A Human chr2 - 86510390 86510390 86510390 AAAGTCTTGTGAAGATTCCAGAGATTCAGGCCACCATGAGGGAGTTGTCCAAAGAAATGATGAAG AAAGTCTTGTGAAGATTCCAGAGATTCAGGCCTCCATGAGGGAGTTGTCCAAAGAAATGATGAAG T A CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86510318..86510390 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_557089,Human_RBP_ID_17962745,Human_RBP_ID_23888040 Human_Splice_Rec_271310,Human_Splice_Rec_271311,Human_Splice_Rec_271319,Human_Splice_Rec_271326,Human_Splice_Rec_271327,Human_Splice_Rec_271336,Human_Splice_Rec_271337,Human_Splice_Rec_271346,Human_Splice_Rec_271347,Human_Splice_Rec_271351,Human_Splice_Rec_271358,Human_Splice_Rec_271376,Human_Splice_Rec_271377,Human_Splice_Rec_271386 RMVar_hsa_circ_201706,RMVar_hsa_circ_300329,RMVar_hsa_circ_359267 114234 RMVar_ID_114234 Human_SNP_ID_835572975 m1A Human chr2 - 42361133 42361133 42361133 CGTCATGTACTACAAGTTTAGTGGCTTCACGCAGAAGTTGGCAGGAGCATGGGCTTCGGAGGCCT CGTCATGTACTACAAGTTTAGTGGCTTCACGCTGAAGTTGGCAGGAGCATGGGCTTCGGAGGCCT T A COX7A2L Ensembl:ENSG00000115944 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 face Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 3 skin,head and neck Human_RBP_ID_280908,Human_RBP_ID_551071,Human_RBP_ID_4623259,Human_RBP_ID_5146532,Human_RBP_ID_8234313,Human_RBP_ID_9106624,Human_RBP_ID_13889055,Human_RBP_ID_22451229,Human_RBP_ID_23872172,Human_RBP_ID_26819690 Human_Splice_Rec_239345,Human_Splice_Rec_239349,Human_Splice_Rec_239355,Human_Splice_Rec_239371 114235 RMVar_ID_114235 Human_SNP_ID_835603105 m1A Human chr2 + 27651465 27651465 27651465 ATTTCCCTCGTCTTGACCATCTGGTGCCTGTTATGCAGTTTAACATTCTGCAGCAATAAAAGTGT ATTTCCCTCGTCTTGACCATCTGGTGCCTGTTCTGCAGTTTAACATTCTGCAGCAATAAAAGTGT A C GPN1 Ensembl:ENSG00000198522 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10201652 Functional Loss SNV ICGC 33..33 33 ESCA 2 - GWAS_ID_11563,GWAS_ID_11564,GWAS_ID_11565,GWAS_ID_11566,GWAS_ID_11567 114236 RMVar_ID_114236 Human_SNP_ID_835612885 m1A Human chr2 + 69181863 69181863 69181863 GACGCCTCTTATTATGGTGGGAGAGGCGTTGGAGGCATTAAAAGAATGGAGGTAAGAGGACAGCT GACGCCTCTTATTATGGTGGGAGAGGCGTTGGGGGCATTAAAAGAATGGAGGTAAGAGGACAGCT A G ANTXR1 Ensembl:ENSG00000169604 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:69181814..69181920 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_18999597 Human_Splice_Rec_255592,Human_Splice_Rec_255593 RMVar_hsa_circ_14788,RMVar_hsa_circ_376828,RMVar_hsa_circ_20066,RMVar_hsa_circ_46173,RMVar_hsa_circ_309555 114237 RMVar_ID_114237 Human_SNP_ID_835617212 m1A Human chr2 + 219208296 219208296 219208296 CCATCTCCAGAGCACAAGCTGTGGCTTCTACAAGCACTGTCCCCAGCCCAAGTCAAACCATGCCT CCATCTCCAGAGCACAAGCTGTGGCTTCTACAGGCACTGTCCCCAGCCCAAGTCAAACCATGCCT A G ZFAND2B Ensembl:ENSG00000158552 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:219208252..219208407 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 10 kidney Human_RBP_ID_19003074,Human_RBP_ID_27819321 Human_Splice_Rec_361324,Human_Splice_Rec_361325,Human_Splice_Rec_361342,Human_Splice_Rec_361352,Human_Splice_Rec_361353,Human_Splice_Rec_361368,Human_Splice_Rec_361369,Human_Splice_Rec_361384,Human_Splice_Rec_361394,Human_Splice_Rec_361395,Human_Splice_Rec_361418,Human_Splice_Rec_361419,Human_Splice_Rec_361430,Human_Splice_Rec_361431,Human_Splice_Rec_361446,Human_Splice_Rec_361456,Human_Splice_Rec_361457,Human_Splice_Rec_361482,Human_Splice_Rec_361483,Human_Splice_Rec_361490,Human_Splice_Rec_361491,Human_Splice_Rec_361498,Human_Splice_Rec_361499,Human_Splice_Rec_361508,Human_Splice_Rec_361509 Human_miRNA_ID_2683257,Human_miRNA_ID_2842606 RMVar_hsa_circ_90494,RMVar_hsa_circ_105912,RMVar_hsa_circ_207065,RMVar_hsa_circ_207067,RMVar_hsa_circ_207069,RMVar_hsa_circ_312541,RMVar_hsa_circ_341946,RMVar_hsa_circ_100093,RMVar_hsa_circ_207068 114238 RMVar_ID_114238 Human_SNP_ID_835619678 m1A Human chr2 + 10791740 10791740 10791740 ATTATCTACTTCAGCTCTTTCAAAATAAGCTAATGAATGTACTGAAAACACTGTGAATGAACAGA ATTATCTACTTCAGCTCTTTCAAAATAAGCTACTGAATGTACTGAAAACACTGTGAATGAACAGA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:10791738..10791825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114239 RMVar_ID_114239 Human_SNP_ID_835635273 m1A Human chr2 - 1743781 1743781 1743781 CCCGAGCGCGGCGCAGCCCCCTCCGTCCTCCCAGCCCCCTCCGCCCCGTTCCTCGTCCTGTTCGC CCCGAGCGCGGCGCAGCCCCCTCCGTCCTCCCCGCCCCCTCCGCCCCGTTCCTCGTCCTGTTCGC T G PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:1743779..1743906 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114240 RMVar_ID_114240 Human_SNP_ID_835635796 m1A Human chr2 + 99361639 99361639 99361639 AAGGAGCGCGAGAGAAAAAAGCGAGATGAAGAAAAAGCGAAACTGCGGAAGCTGAAAGAAAAAGA AAGGAGCGCGAGAGAAAAAAGCGAGATGAAGAGAAAGCGAAACTGCGGAAGCTGAAAGAAAAAGA A G EIF5B Ensembl:ENSG00000158417 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:99361155..99361730 26863196 MeRIP-seq:(Medium) rs747600510 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_61509,Human_RBP_ID_205336,Human_RBP_ID_1592230,Human_RBP_ID_2669885,Human_RBP_ID_4622111,Human_RBP_ID_9347220,Human_RBP_ID_23115047,Human_RBP_ID_23891496,Human_RBP_ID_24545821 RMVar_hsa_circ_55926,RMVar_hsa_circ_64628,RMVar_hsa_circ_352749,RMVar_hsa_circ_74538 114241 RMVar_ID_114241 Human_SNP_ID_835644616 m1A Human chr2 - 210002645 210002645 210002645 TGCAGCCCGACGCCATACCGCTGGCTCCCAAAAGCAAGTTACCCACGAGTCCCCGGCAAGGCTAG TGCAGCCCGACGCCATACCGCTGGCTCCCAAAGGCAAGTTACCCACGAGTCCCCGGCAAGGCTAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:210002617..210002739;chr2:210002605..210002832;chr2:210002604..210002763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 11 lung 114242 RMVar_ID_114242 Human_SNP_ID_835652234 m1A Human chr2 + 86108401 86108401 86108401 ACCCTCTCAAAGGTTGAAGGAACTGATGTAACAGGTATATTTTAAAATATATTGAATTCTATTTT ACCCTCTCAAAGGTTGAAGGAACTGATGTAACCGGTATATTTTAAAATATATTGAATTCTATTTT A C PTCD3 Ensembl:ENSG00000132300 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:86107196..86108538 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach Human_RBP_ID_3958008,Human_RBP_ID_18999820 Human_Splice_Rec_270484,Human_Splice_Rec_270485,Human_Splice_Rec_270494,Human_Splice_Rec_270495,Human_Splice_Rec_270510,Human_Splice_Rec_270511,Human_Splice_Rec_270524,Human_Splice_Rec_270525,Human_Splice_Rec_270532,Human_Splice_Rec_270533,Human_Splice_Rec_270542,Human_Splice_Rec_270543,Human_Splice_Rec_270586,Human_Splice_Rec_270587,Human_Splice_Rec_270590,Human_Splice_Rec_270591,Human_Splice_Rec_270595 RMVar_hsa_circ_64408,RMVar_hsa_circ_125766,RMVar_hsa_circ_302975,RMVar_hsa_circ_346100,RMVar_hsa_circ_320993,RMVar_hsa_circ_288995,RMVar_hsa_circ_71301,RMVar_hsa_circ_95968,RMVar_hsa_circ_64529,RMVar_hsa_circ_201629,RMVar_hsa_circ_201630,RMVar_hsa_circ_201631,RMVar_hsa_circ_201628 114243 RMVar_ID_114243 Human_SNP_ID_835654924 m1A Human chr2 + 196926629 196926629 196926629 TTAACTGAGTGAAGAAACATGGTGCCGCCACCACCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC TTAACTGAGTGAAGAAACATGGTGCCGCCACCGCCGCCGCCGCCGCCGCCGCCCCCTCTACCTCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr2:196926580..196926733;chr2:196926601..196926725 26863196 MeRIP-seq:(Medium) rs963651695 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 114244 RMVar_ID_114244 Human_SNP_ID_835656530 m1A Human chr2 - 197497294 197497294 197497294 GCAAAGTCAATTGACTTAAAAGATAAATACAAAAACATTGGAGCTAAACTTGTTCAAGATGTTGC GCAAAGTCAATTGACTTAAAAGATAAATACAAGAACATTGGAGCTAAACTTGTTCAAGATGTTGC T C HSPD1 Ensembl:ENSG00000144381 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8539 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 11 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_59507,Human_RBP_ID_1581866,Human_RBP_ID_1906812,Human_RBP_ID_22246517,Human_RBP_ID_26488131,Human_RBP_ID_27005323,Human_RBP_ID_27285241 Human_Splice_Rec_342306,Human_Splice_Rec_342326,Human_Splice_Rec_342354,Human_Splice_Rec_342368,Human_Splice_Rec_342376,Human_Splice_Rec_342384,Human_Splice_Rec_342390,Human_Splice_Rec_342394,Human_Splice_Rec_342400,Human_Splice_Rec_342406 Clinvar_Rec_464 GWAS_ID_10597,GWAS_ID_10598,GWAS_ID_10599,GWAS_ID_10600,GWAS_ID_10601,GWAS_ID_10602 RMVar_hsa_circ_115375,RMVar_hsa_circ_87075,RMVar_hsa_circ_205685,RMVar_hsa_circ_205686,RMVar_hsa_circ_126781,RMVar_hsa_circ_57034,RMVar_hsa_circ_205687,RMVar_hsa_circ_122492,RMVar_hsa_circ_205691,RMVar_hsa_circ_332331,RMVar_hsa_circ_205695,RMVar_hsa_circ_94462,RMVar_hsa_circ_281585,RMVar_hsa_circ_205698,RMVar_hsa_circ_345564 114245 RMVar_ID_114245 Human_SNP_ID_835706698 m1A Human chr2 + 210677072 210677072 210677072 TAACCTTCCCAACAACAACACTAAATTTGTCCATGATAATTATGTGATTCGGAGGACAGCTGTTG TAACCTTCCCAACAACAACACTAAATTTGTCCCTGATAATTATGTGATTCGGAGGACAGCTGTTG A C CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210676974..210677170 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_56032,Human_RBP_ID_13762444,Human_RBP_ID_17191600,Human_RBP_ID_20437070 Human_Splice_Rec_353154,Human_Splice_Rec_353155,Human_Splice_Rec_353232,Human_Splice_Rec_353233,Human_Splice_Rec_353308,Human_Splice_Rec_353309,Human_Splice_Rec_353384,Human_Splice_Rec_353385,Human_Splice_Rec_353458,Human_Splice_Rec_353459,Human_Splice_Rec_353540,Human_Splice_Rec_353541,Human_Splice_Rec_353594,Human_Splice_Rec_353595,Human_Splice_Rec_353644,Human_Splice_Rec_353645,Human_Splice_Rec_353674,Human_Splice_Rec_353675,Human_Splice_Rec_353688,Human_Splice_Rec_353692,Human_Splice_Rec_353693 Human_miRNA_ID_688024,Human_miRNA_ID_2276138 RMVar_hsa_circ_35167,RMVar_hsa_circ_358533,RMVar_hsa_circ_368273,RMVar_hsa_circ_56784,RMVar_hsa_circ_71865,RMVar_hsa_circ_70591,RMVar_hsa_circ_113456,RMVar_hsa_circ_108453,RMVar_hsa_circ_206578,RMVar_hsa_circ_359583,RMVar_hsa_circ_206579 114246 RMVar_ID_114246 Human_SNP_ID_835721210 m1A Human chr2 - 127048584 127048584 127048584 GGGCGTGAAGGAGAGCGACTGGAACCAGCACAAGGAGCTGGAGAAGTGCCGTGGCGTCTTCCCCG GGGCGTGAAGGAGAGCGACTGGAACCAGCACAGGGAGCTGGAGAAGTGCCGTGGCGTCTTCCCCG T C BIN1 Ensembl:ENSG00000136717 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:127048533..127048657 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 11 head and neck Human_Splice_Rec_294132,Human_Splice_Rec_294166,Human_Splice_Rec_294194,Human_Splice_Rec_294218,Human_Splice_Rec_294248,Human_Splice_Rec_294278,Human_Splice_Rec_294306,Human_Splice_Rec_294336,Human_Splice_Rec_294364,Human_Splice_Rec_294400,Human_Splice_Rec_294408,Human_Splice_Rec_294434 114247 RMVar_ID_114247 Human_SNP_ID_835732425 m1A Human chr2 - 224585201 224585195 224585201 CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCGAGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGC CCCCCCAGCCGCATCGGAGTCGCCAGAGTCCG______CGCCGCCGCCGCCGCCGCCCCCGCCGC GGCGGCT G CUL3 Ensembl:ENSG00000036257 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEK293T cell line,total RNA;HEK293T,Starvation treatment chr2:224584948..224585425;chr2:224585037..224585289;chr2:224585051..224585291;chr2:224585032..224585350;chr2:224585110..224585349 26863196,26863410 MeRIP-seq:(Medium) rs1428627934 Functional Loss DEL ICGC 33..38 33 LMS 1 - Human_RBP_ID_4625152 114248 RMVar_ID_114248 Human_SNP_ID_835732768 m1A Human chr2 + 176093073 176093073 176093073 GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCAGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC GGGACGCATTCGGGGCGGGCGGCGGCGGCGGCGGCGGCGGCTGCGGCGGCGGCGGCGGCAGCCTC A G HOXD13 Ensembl:ENSG00000128714 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:176092976..176093200 26863410 MeRIP-seq:(Medium) rs540457957 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_538755 114249 RMVar_ID_114249 Human_SNP_ID_835736973 m1A Human chr2 - 38297345 38297345 38297345 AATGAAAGCTACGGTTATTAATGACGAACGCTATAATAGGCATTTGAGATGCCATTTTTGGGCTC AATGAAAGCTACGGTTATTAATGACGAACGCTGTAATAGGCATTTGAGATGCCATTTTTGGGCTC T C ATL2 Ensembl:ENSG00000119787 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3213959 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_27011524,Human_RBP_ID_27479995 GWAS_ID_8957,GWAS_ID_8958,GWAS_ID_8959,GWAS_ID_8960,GWAS_ID_8961,GWAS_ID_8962,GWAS_ID_8963,GWAS_ID_8964,GWAS_ID_8965,GWAS_ID_8966,GWAS_ID_8967,GWAS_ID_8968,GWAS_ID_8969,GWAS_ID_8970,GWAS_ID_8971,GWAS_ID_8972,GWAS_ID_8973,GWAS_ID_8974,GWAS_ID_8975,GWAS_ID_8976,GWAS_ID_8977,GWAS_ID_8978,GWAS_ID_8979,GWAS_ID_8980,GWAS_ID_8981,GWAS_ID_8982,GWAS_ID_8983,GWAS_ID_8984,GWAS_ID_8985,GWAS_ID_8986,GWAS_ID_8987,GWAS_ID_8988,GWAS_ID_8989,GWAS_ID_8990,GWAS_ID_8991,GWAS_ID_8992,GWAS_ID_8993,GWAS_ID_8994,GWAS_ID_8995,GWAS_ID_8996,GWAS_ID_8997,GWAS_ID_8998,GWAS_ID_8999,GWAS_ID_9000,GWAS_ID_9001,GWAS_ID_9002,GWAS_ID_9003,GWAS_ID_9004,GWAS_ID_9005,GWAS_ID_9006,GWAS_ID_9007,GWAS_ID_9008,GWAS_ID_9009,GWAS_ID_9010,GWAS_ID_9011,GWAS_ID_9012,GWAS_ID_9013,GWAS_ID_9014,GWAS_ID_9015,GWAS_ID_9016 114250 RMVar_ID_114250 Human_SNP_ID_835745957 m1A Human chr2 - 176201133 176201133 176201133 GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAACCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAGCCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs563303838 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1064025,Human_RBP_ID_5275510,Human_RBP_ID_18750240,Human_RBP_ID_26488082 114251 RMVar_ID_114251 Human_SNP_ID_835755553 m1A Human chr2 - 160407555 160407555 160407555 CGAGGCTGCCCCGCGCCCGCGCCCGCGCCCGCACCCGCCGCCGCCGCCCGCAGCGATGATCTTCC CGAGGCTGCCCCGCGCCCGCGCCCGCGCCCGCGCCCGCCGCCGCCGCCCGCAGCGATGATCTTCC T C RBMS1 Ensembl:ENSG00000153250 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:160407538..160407679 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_3638902,Human_RBP_ID_26787223 Human_Splice_Rec_313411 RMVar_hsa_circ_1320 114252 RMVar_ID_114252 Human_SNP_ID_835790257 m1A Human chr2 - 232528625 232528625 232528625 CCTGAACTTGAGGGAGCAGTTCTGCCAGTCGAAGGGGAAATAGGTGACAGAGATGGGGCAGGAGG CCTGAACTTGAGGGAGCAGTTCTGCCAGTCGATGGGGAAATAGGTGACAGAGATGGGGCAGGAGG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:232528469..232528652 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 4 lung 114253 RMVar_ID_114253 Human_SNP_ID_835790611 m1A Human chr2 - 65313731 65313731 65313731 CCGTGAGAACTTGCATCCGCCGGGTGAGCTGCATGTGGTGCGCGGACAGCATGCTCTATCACTGT CCGTGAGAACTTGCATCCGCCGGGTGAGCTGCGTGTGGTGCGCGGACAGCATGCTCTATCACTGT T C SPRED2 Ensembl:ENSG00000198369 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:65313680..65313875 32194978 MeRIP-seq:(Medium) rs1269855441 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_18764150,Human_RBP_ID_22076326,Human_RBP_ID_27481238 Human_miRNA_ID_205432,Human_miRNA_ID_2011396,Human_miRNA_ID_2757754 RMVar_hsa_circ_104607,RMVar_hsa_circ_200787 114254 RMVar_ID_114254 Human_SNP_ID_835808154 m1A Human chr2 - 74362143 74362143 74362143 AAATGAACCCTTGTCTTCCTCTCCCCTTCCCTAGGATGAGGTCCTCAAGGAGACAGTATCTCAGC AAATGAACCCTTGTCTTCCTCTCCCCTTCCCTTGGATGAGGTCCTCAAGGAGACAGTATCTCAGC T A AC006030.1,DCTN1 Ensembl:ENSG00000264324,Ensembl:ENSG00000204843 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74362116..74362750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 9 liver Human_RBP_ID_4616785 Human_Splice_Rec_263373,Human_Splice_Rec_263963,Human_Splice_Rec_264023,Human_Splice_Rec_264083,Human_Splice_Rec_264091,Human_Splice_Rec_264145,Human_Splice_Rec_264197,Human_Splice_Rec_264247,Human_Splice_Rec_264301,Human_Splice_Rec_264361,Human_Splice_Rec_264399,Human_Splice_Rec_264453 Human_miRNA_ID_1961390,Human_miRNA_ID_1961391,Human_miRNA_ID_1961392 RMVar_hsa_circ_95900,RMVar_hsa_circ_201310,RMVar_hsa_circ_105012,RMVar_hsa_circ_97781,RMVar_hsa_circ_127386,RMVar_hsa_circ_117499,RMVar_hsa_circ_97127,RMVar_hsa_circ_201318,RMVar_hsa_circ_201322,RMVar_hsa_circ_90269,RMVar_hsa_circ_92205,RMVar_hsa_circ_87494,RMVar_hsa_circ_201323,RMVar_hsa_circ_201320,RMVar_hsa_circ_201321,RMVar_hsa_circ_201319,RMVar_hsa_circ_201316,RMVar_hsa_circ_201317 114255 RMVar_ID_114255 Human_SNP_ID_835823247 m1A Human chr2 + 46576118 46576118 46576118 GGAAGACTATGACCGTCTGAGGCCTTTATCTTACCCAATGACCGATGTCTTCCTTATATGCTTCT GGAAGACTATGACCGTCTGAGGCCTTTATCTTGCCCAATGACCGATGTCTTCCTTATATGCTTCT A G RHOQ Ensembl:ENSG00000119729 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46576093..46576166 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_551654,Human_RBP_ID_1587250,Human_RBP_ID_8848448,Human_RBP_ID_17957742,Human_RBP_ID_18761613,Human_RBP_ID_23874241,Human_RBP_ID_27480378 Human_Splice_Rec_242094,Human_Splice_Rec_242098,Human_Splice_Rec_242104,Human_Splice_Rec_242112,Human_Splice_Rec_242118,Human_Splice_Rec_242124 Human_miRNA_ID_1041346 RMVar_hsa_circ_300877 114256 RMVar_ID_114256 Human_SNP_ID_835896841 m1A Human chr2 + 159227962 159227962 159227962 TATCTCAATTTGTCGCGATGCCGAAGAAAAACAAATGTAAGCTGTGCCCCTTTATTCCAACCCAG TATCTCAATTTGTCGCGATGCCGAAGAAAAACCAATGTAAGCTGTGCCCCTTTATTCCAACCCAG A C TANC1 Ensembl:ENSG00000115183 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2288110 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_19098332 Human_Splice_Rec_312133,Human_Splice_Rec_312151 GWAS_ID_7457,GWAS_ID_7458,GWAS_ID_7459,GWAS_ID_7460,GWAS_ID_7461 RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_89610,RMVar_hsa_circ_204040,RMVar_hsa_circ_204041 114257 RMVar_ID_114257 Human_SNP_ID_835910229 m1A Human chr2 + 188997236 188997236 188997236 GGACCTGGCCCTCAGGTACGTAGCTTTCCTCAATTTATTTCTAGCCTTCTAATAGATGCGTTCAT GGACCTGGCCCTCAGGTACGTAGCTTTCCTCAGTTTATTTCTAGCCTTCTAATAGATGCGTTCAT A G COL3A1 Ensembl:ENSG00000168542 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:188997234..188997321 26863196 MeRIP-seq:(Medium) rs28413125 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA 3 stomach Human_Splice_Rec_336312,Human_Splice_Rec_336412 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_89524,RMVar_hsa_circ_56534,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_79379,RMVar_hsa_circ_205218 114258 RMVar_ID_114258 Human_SNP_ID_835915272 m1A Human chr2 + 191010248 191010248 191010248 ATCTTCATGTCTTTGCTTATTGTCAACATATCAGGGCAGCCTTCTCTGGCCTCTTTTATTTAAAC ATCTTCATGTCTTTGCTTATTGTCAACATATCGGGGCAGCCTTCTCTGGCCTCTTTTATTTAAAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:191010245..191010328 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114259 RMVar_ID_114259 Human_SNP_ID_835924330 m1A Human chr2 - 68293908 68293908 68293908 CTTCTCTGTCATTGAGTATGAATGCAAGCCCAACGAGACACGCAGTCTGATGTGGGTGAACAAGG CTTCTCTGTCATTGAGTATGAATGCAAGCCCAGCGAGACACGCAGTCTGATGTGGGTGAACAAGG T C CNRIP1 Ensembl:ENSG00000119865 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:68293744..68315939 32194978 MeRIP-seq:(Medium) rs148723232 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_23881393 Human_miRNA_ID_2141149 RMVar_hsa_circ_79430,RMVar_hsa_circ_200835 114260 RMVar_ID_114260 Human_SNP_ID_835927240 m1A Human chr2 + 74464626 74464626 74464626 TGTGTTGGCGCCCGAAGGAGAGGCCGTCGTGGAACTCCCAGCCATAGGGACCCACACCGTCCCCC TGTGTTGGCGCCCGAAGGAGAGGCCGTCGTGGCACTCCCAGCCATAGGGACCCACACCGTCCCCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74464575..74464760 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck 114261 RMVar_ID_114261 Human_SNP_ID_835928443 m1A Human chr2 + 131492245 131492245 131492245 ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGAGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT ACGTCGGGGTCGATACCGCCGCCCGCCGCCTGCGCCAGCTCGTACAGCTCCATCTCCTCGGTGCT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:131492226..131492300 26863196 MeRIP-seq:(Medium) rs1042999 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck 114262 RMVar_ID_114262 Human_SNP_ID_835936291 m1A Human chr2 + 15596745 15596745 15596745 AACTTTTTTCCCCTCATTCAGGCTGCAGAAACAGGAAGTGGCAAAACTGGTGTAAGTAATAAATT AACTTTTTTCCCCTCATTCAGGCTGCAGAAACTGGAAGTGGCAAAACTGGTGTAAGTAATAAATT A T DDX1 Ensembl:ENSG00000079785 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:15596726..15596775 26863196 MeRIP-seq:(Medium) rs766867235 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_922540,Human_RBP_ID_3958685,Human_RBP_ID_5378230,Human_RBP_ID_9347072,Human_RBP_ID_13650949,Human_RBP_ID_19096938,Human_RBP_ID_22667030,Human_RBP_ID_23211448,Human_RBP_ID_25574476,Human_RBP_ID_26786784 Human_Splice_Rec_219728,Human_Splice_Rec_219729,Human_Splice_Rec_219822,Human_Splice_Rec_219823 RMVar_hsa_circ_1836,RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_371153,RMVar_hsa_circ_344483,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197263,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_360164,RMVar_hsa_circ_197265,RMVar_hsa_circ_19463 114263 RMVar_ID_114263 Human_SNP_ID_835942655 m1A Human chr2 - 119367057 119367057 119367057 TTCGCAGCCTGGCTGTGCACGCGCTGTACCTGAGACATCCTGGCCGACTTGCAAGAACTCCAGGG TTCGCAGCCTGGCTGTGCACGCGCTGTACCTGCGACATCCTGGCCGACTTGCAAGAACTCCAGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:119366976..119367116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 8 liver 114264 RMVar_ID_114264 Human_SNP_ID_835980447 m1A Human chr2 + 206162554 206162554 206162554 TAGATGTGAAACCTTGGGATGATGAGACAGATATGGCGAAATTAGAGGAGTGCGTCAGAAGCATT TAGATGTGAAACCTTGGGATGATGAGACAGATTTGGCGAAATTAGAGGAGTGCGTCAGAAGCATT A T EEF1B2 Ensembl:ENSG00000114942 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:206162526..206162600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney Human_RBP_ID_542986,Human_RBP_ID_1582744,Human_RBP_ID_1908763,Human_RBP_ID_3612768,Human_RBP_ID_9101403,Human_RBP_ID_13753281,Human_RBP_ID_23892928 Human_Splice_Rec_350044,Human_Splice_Rec_350045,Human_Splice_Rec_350056,Human_Splice_Rec_350057,Human_Splice_Rec_350082,Human_Splice_Rec_350083,Human_Splice_Rec_350094,Human_Splice_Rec_350095,Human_Splice_Rec_350114,Human_Splice_Rec_350115,Human_Splice_Rec_350117 Human_miRNA_ID_1388937,Human_miRNA_ID_2707895,Human_miRNA_ID_2707896 RMVar_hsa_circ_94738,RMVar_hsa_circ_95655,RMVar_hsa_circ_206342,RMVar_hsa_circ_206346 114265 RMVar_ID_114265 Human_SNP_ID_836014244 m1A Human chr2 - 135985513 135985513 135985513 GAGGGAGAAGCCCCTTTGGCCTGCCTTACGGAAGCCTGCGAGGGAGGGTGGTGTCCACTGCCCAG GAGGGAGAAGCCCCTTTGGCCTGCCTTACGGAGGCCTGCGAGGGAGGGTGGTGTCCACTGCCCAG T C DARS1 Ensembl:ENSG00000115866 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:135985469..135985582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_535062,Human_RBP_ID_775358,Human_RBP_ID_829213,Human_RBP_ID_4582670,Human_RBP_ID_5322642,Human_RBP_ID_9296825,Human_RBP_ID_9330683,Human_RBP_ID_17392801,Human_RBP_ID_23826896,Human_RBP_ID_26338696 RMVar_hsa_circ_203508,RMVar_hsa_circ_109256 114266 RMVar_ID_114266 Human_SNP_ID_836054841 m1A Human chr2 + 207754755 207754755 207754755 AACTTCCTGGTCTCAAGCCATCCTCTAGCCTCAGCCACACAAGTAGCTGGGACTACAAGTGCAAC AACTTCCTGGTCTCAAGCCATCCTCTAGCCTCGGCCACACAAGTAGCTGGGACTACAAGTGCAAC A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_17570159 Human_miRNA_ID_2075376 RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 114267 RMVar_ID_114267 Human_SNP_ID_836058404 m1A Human chr2 - 218401633 218401633 218401633 GAGCAGGCAGGGCCTCCCCATCATCCCGGCAGACACAGCAGAAGAGTGAGTGGAGGATGCCCCGG GAGCAGGCAGGGCCTCCCCATCATCCCGGCAGCCACAGCAGAAGAGTGAGTGGAGGATGCCCCGG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218401584..218401685 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 114268 RMVar_ID_114268 Human_SNP_ID_836077154 m1A Human chr2 - 101253046 101253046 101253046 GCCGGAGCCCCCGAAGCCGCTCCTGGACGCCGACCCTGCCGCTTCCCGGGACCCTCTTTGCTCCG GCCGGAGCCCCCGAAGCCGCTCCTGGACGCCGCCCCTGCCGCTTCCCGGGACCCTCTTTGCTCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:101252901..101253175 26863196 MeRIP-seq:(Medium) rs913464922 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114269 RMVar_ID_114269 Human_SNP_ID_836077868 m1A Human chr2 - 29115732 29115732 29115732 ACTGACCTCCCCGCGGGCCCCCAGGGCCGCCCACCCCGGCCCCAACCCCGCCGCCGGCCAGCCCG ACTGACCTCCCCGCGGGCCCCCAGGGCCGCCCCCCCCGGCCCCAACCCCGCCGCCGGCCAGCCCG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:29115711..29115921 26863196 MeRIP-seq:(Medium) rs913914018 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114270 RMVar_ID_114270 Human_SNP_ID_836095359 m1A Human chr2 + 232379777 232379777 232379777 TGACCTCTGACACCCTTAGGGAAGTCAGTGGGAGTGGTAACCACCACACGAGTGCAGCACGCCTC TGACCTCTGACACCCTTAGGGAAGTCAGTGGGCGTGGTAACCACCACACGAGTGCAGCACGCCTC A C ALPP Ensembl:ENSG00000163283 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232379690..232379776 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_26480517 Human_Splice_Rec_370648 114271 RMVar_ID_114271 Human_SNP_ID_836095802 m1A Human chr2 + 73780052 73780052 73780052 CGCCAGTCCGGCGCCCTCAATGCCAGGATAAGACCCTAAACAGGAAAAGACTCGGCAGCCACCTA CGCCAGTCCGGCGCCCTCAATGCCAGGATAAGGCCCTAAACAGGAAAAGACTCGGCAGCCACCTA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:73779940..73780065 26863196 MeRIP-seq:(Medium) rs770537593 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 114272 RMVar_ID_114272 Human_SNP_ID_836115464 m1A Human chr2 - 238173606 238173606 238173606 GGGCGTGCTAGAGGTGTCACGCTCCATTGGGGACGGGCAGTACAAGCGCTGCGGTGTCACCTCTG GGGCGTGCTAGAGGTGTCACGCTCCATTGGGGGCGGGCAGTACAAGCGCTGCGGTGTCACCTCTG T C ILKAP Ensembl:ENSG00000132323 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:238173555..238173705 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_546479,Human_RBP_ID_19000952,Human_RBP_ID_22669819 Human_Splice_Rec_376741,Human_Splice_Rec_376760,Human_Splice_Rec_376761,Human_Splice_Rec_376782,Human_Splice_Rec_376783,Human_Splice_Rec_376798,Human_Splice_Rec_376799,Human_Splice_Rec_376818,Human_Splice_Rec_376819,Human_Splice_Rec_376828,Human_Splice_Rec_376829,Human_Splice_Rec_376838,Human_Splice_Rec_376839 RMVar_hsa_circ_102288,RMVar_hsa_circ_123301,RMVar_hsa_circ_127145,RMVar_hsa_circ_110884,RMVar_hsa_circ_104503,RMVar_hsa_circ_207874,RMVar_hsa_circ_207863,RMVar_hsa_circ_207867,RMVar_hsa_circ_87670,RMVar_hsa_circ_95089,RMVar_hsa_circ_207868,RMVar_hsa_circ_207865,RMVar_hsa_circ_207866,RMVar_hsa_circ_207864,RMVar_hsa_circ_315412,RMVar_hsa_circ_266652,RMVar_hsa_circ_354175,RMVar_hsa_circ_207862,RMVar_hsa_circ_378997,RMVar_hsa_circ_269568,RMVar_hsa_circ_322989,RMVar_hsa_circ_207870,RMVar_hsa_circ_322830,RMVar_hsa_circ_120753,RMVar_hsa_circ_297484,RMVar_hsa_circ_207876,RMVar_hsa_circ_85776,RMVar_hsa_circ_207875,RMVar_hsa_circ_207872,RMVar_hsa_circ_207873,RMVar_hsa_circ_207871 114273 RMVar_ID_114273 Human_SNP_ID_836139257 m1A Human chr2 + 230877451 230877451 230877451 AGACGTACATCATCCAGGAGGAGATGGTGGTCACGGAGCATGTCAGTGACAAGGAGGCCCTGGGG AGACGTACATCATCCAGGAGGAGATGGTGGTCGCGGAGCATGTCAGTGACAAGGAGGCCCTGGGG A G ITM2C Ensembl:ENSG00000135916 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:230877401..230877569 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_545595,Human_RBP_ID_9103791,Human_RBP_ID_17952031,Human_RBP_ID_22766300 Human_Splice_Rec_369148,Human_Splice_Rec_369149,Human_Splice_Rec_369156,Human_Splice_Rec_369157,Human_Splice_Rec_369164,Human_Splice_Rec_369165,Human_Splice_Rec_369180,Human_Splice_Rec_369181 114274 RMVar_ID_114274 Human_SNP_ID_836151726 m1A Human chr2 + 101253221 101253221 101253221 ATCGGAGGAGGCGGGCGGCGGCAGCACCTTCGAGGGCCTGTCCACCGCCTTCCACCACTACTTCA ATCGGAGGAGGCGGGCGGCGGCAGCACCTTCGGGGGCCTGTCCACCGCCTTCCACCACTACTTCA A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114275 RMVar_ID_114275 Human_SNP_ID_836168981 m1A Human chr2 - 73234386 73234386 73234386 GCTGATGGCGACGGATGCGCGAGACGCCACTCACCATCATTTTGGAAGCTTATTCAGCGGCCCGC GCTGATGGCGACGGATGCGCGAGACGCCACTCGCCATCATTTTGGAAGCTTATTCAGCGGCCCGC T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr2:73234301..73234446;chr2:73234326..73234449 26863410 MeRIP-seq:(Medium) rs1273145904 Functional Loss SNV ICGC 33..33 33 STAD 1 - 114276 RMVar_ID_114276 Human_SNP_ID_836195209 m1A Human chr2 - 73239692 73239692 73239692 GGCAGGCACTGATGTTACTCACAAGCTGGGGGATGCCTTGGGAGCTATCAGTCCCCTCTTTCAAT GGCAGGCACTGATGTTACTCACAAGCTGGGGGGTGCCTTGGGAGCTATCAGTCCCCTCTTTCAAT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr2:73239597..73239793;chr2:73239626..73239800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 114277 RMVar_ID_114277 Human_SNP_ID_836209587 m1A Human chr2 + 240592062 240592062 240592062 GTAGCAGGAAGCGGAGGCCAGCAGGACAGGCCAGGCCGCTGGGAGCACAGGACTTGTCGGCAGCT GTAGCAGGAAGCGGAGGCCAGCAGGACAGGCCGGGCCGCTGGGAGCACAGGACTTGTCGGCAGCT A G CAPN10 Ensembl:ENSG00000142330 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:240592017..240592118 26863196 MeRIP-seq:(Medium) rs3792269 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_RBP_ID_242891,Human_RBP_ID_19003475 Human_Splice_Rec_378213,Human_Splice_Rec_378233,Human_Splice_Rec_378263,Human_Splice_Rec_378283,Human_Splice_Rec_378305,Human_Splice_Rec_378323,Human_Splice_Rec_378343,Human_Splice_Rec_378357,Human_Splice_Rec_378373 Clinvar_Rec_228 GWAS_ID_7637,GWAS_ID_7638,GWAS_ID_7639,GWAS_ID_7640,GWAS_ID_7641,GWAS_ID_7642,GWAS_ID_7643,GWAS_ID_7644,GWAS_ID_7645,GWAS_ID_7646,GWAS_ID_7647,GWAS_ID_7648,GWAS_ID_7649,GWAS_ID_7650,GWAS_ID_7651,GWAS_ID_7652,GWAS_ID_7653,GWAS_ID_7654,GWAS_ID_7655,GWAS_ID_7656,GWAS_ID_7657,GWAS_ID_7658,GWAS_ID_7659,GWAS_ID_7660,GWAS_ID_7661,GWAS_ID_7662,GWAS_ID_7663,GWAS_ID_7664,GWAS_ID_7665,GWAS_ID_7666 RMVar_hsa_circ_4606,RMVar_hsa_circ_340379,RMVar_hsa_circ_103084,RMVar_hsa_circ_207984 114278 RMVar_ID_114278 Human_SNP_ID_836216384 m1A Human chr2 - 231460703 231460700 231460703 GACGACGAAGATGATGAAGATGATGATGATGAAGATGATGAGGAGGAGGAAGAAGAGGAGGAGGA GACGACGAAGATGATGAAGATGATGATGATGA___TGATGAGGAGGAGGAAGAAGAGGAGGAGGA ATCT A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:231460476..231460906 26863196 MeRIP-seq:(Medium) rs746082903 Functional Loss DEL TCGA 33..35 33 READ 1 - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627046,Human_RBP_ID_3618015,Human_RBP_ID_4599478,Human_RBP_ID_6895102,Human_RBP_ID_8257486,Human_RBP_ID_8513811,Human_RBP_ID_8846342,Human_RBP_ID_9385634,Human_RBP_ID_17390553,Human_RBP_ID_17506476,Human_RBP_ID_17952194,Human_RBP_ID_18533502,Human_RBP_ID_18544615,Human_RBP_ID_18755774,Human_RBP_ID_22006106,Human_RBP_ID_22743085,Human_RBP_ID_22766307,Human_RBP_ID_22814994,Human_RBP_ID_22990285,Human_RBP_ID_23115003,Human_RBP_ID_23119354,Human_RBP_ID_23856671,Human_RBP_ID_24545950,Human_RBP_ID_24560276,Human_RBP_ID_26338841,Human_RBP_ID_27007797,Human_RBP_ID_27478262,Human_RBP_ID_27818060 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 114279 RMVar_ID_114279 Human_SNP_ID_836247400 m1A Human chr2 - 152717358 152717358 152717358 GGCCGGGGACGGGAGCTGAGCGTGGAGGCCTCATGGTGAGTGAAATGGAGAGCCATCCTCCCTCG GGCCGGGGACGGGAGCTGAGCGTGGAGGCCTCGTGGTGAGTGAAATGGAGAGCCATCCTCCCTCG T C PRPF40A Ensembl:ENSG00000196504 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:152717351..152717425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_243222,Human_RBP_ID_4623670,Human_RBP_ID_8851587,Human_RBP_ID_9259902,Human_RBP_ID_9296837,Human_RBP_ID_9331194,Human_RBP_ID_18421915,Human_RBP_ID_19000268,Human_RBP_ID_19098321,Human_RBP_ID_22997206,Human_RBP_ID_23830652,Human_RBP_ID_26339984 Human_Splice_Rec_310069,Human_Splice_Rec_310129,Human_Splice_Rec_310195,Human_Splice_Rec_310214,Human_Splice_Rec_310215,Human_Splice_Rec_310221 RMVar_hsa_circ_79634,RMVar_hsa_circ_203921,RMVar_hsa_circ_90444,RMVar_hsa_circ_203930 114280 RMVar_ID_114280 Human_SNP_ID_836257556 m1A Human chr2 - 74432635 74432635 74432635 GGACACGGAGTTGCAGAGGAAGCTAGACCATGAGATCCGGATGAGGGAAGGGGCCTGTAAGCTGC GGACACGGAGTTGCAGAGGAAGCTAGACCATGCGATCCGGATGAGGGAAGGGGCCTGTAAGCTGC T G RTKN Ensembl:ENSG00000114993 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:74432548..74432711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_830821,Human_RBP_ID_9384070,Human_RBP_ID_13967292,Human_RBP_ID_18999700,Human_RBP_ID_22742968,Human_RBP_ID_22997372 Human_Splice_Rec_264742,Human_Splice_Rec_264766,Human_Splice_Rec_264788,Human_Splice_Rec_264830,Human_Splice_Rec_264834,Human_Splice_Rec_264836,Human_Splice_Rec_264838 RMVar_hsa_circ_90788,RMVar_hsa_circ_201352,RMVar_hsa_circ_323397 114281 RMVar_ID_114281 Human_SNP_ID_836338006 m1A Human chr2 + 32039476 32039476 32039476 GCTCTGGCTCCATGGCGGACCCTGCAAGTCACAGTCCCCGGATACCAGTCTTGGAAAACAAGAAG GCTCTGGCTCCATGGCGGACCCTGCAAGTCACTGTCCCCGGATACCAGTCTTGGAAAACAAGAAG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:32039426..32039500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 114282 RMVar_ID_114282 Human_SNP_ID_836425744 m1A Human chr2 - 241752001 241752001 241752001 CCAGGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGC CCAGGTCCCGGTAACAGTGACCAATGGCTCCCCCTATCCAGGCCCCGGTGACGGTGACCGAGGGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA Glucose starvation 4h chr2:241751839..241752095;chr2:241751739..241752208 26863196 MeRIP-seq:(Medium) rs866135021 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 4 brain 114283 RMVar_ID_114283 Human_SNP_ID_836437199 m1A Human chr2 + 236001117 236001117 236001117 GGGGAGGGGATGGACCCTCAGAGGCGAGACGGACGTACAGGAAACACCACATGGAGACTCTGGCG GGGGAGGGGATGGACCCTCAGAGGCGAGACGGGCGTACAGGAAACACCACATGGAGACTCTGGCG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:236001107..236001182 26863196 MeRIP-seq:(Medium) rs541761942 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_6399,RMVar_hsa_circ_44106,RMVar_hsa_circ_98943,RMVar_hsa_circ_207773,RMVar_hsa_circ_367251,RMVar_hsa_circ_90630,RMVar_hsa_circ_207787,RMVar_hsa_circ_315821,RMVar_hsa_circ_207790 114284 RMVar_ID_114284 Human_SNP_ID_836444747 m1A Human chr2 + 36356229 36356229 36356229 GGTGCGGCGGCGGCGGCGCGTGTGCCCCGCGCAGGGGAGGGCGCCCGCCCCGCTCCCGGCCCGGC GGTGCGGCGGCGGCGGCGCGTGTGCCCCGCGCGGGGGAGGGCGCCCGCCCCGCTCCCGGCCCGGC A G CRIM1 Ensembl:ENSG00000150938 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:36356105..36356278 26863410 MeRIP-seq:(Medium) rs996779162 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_4622347,Human_RBP_ID_5239994,Human_RBP_ID_22450280 Human_miRNA_ID_2387817,Human_miRNA_ID_3030022,Human_miRNA_ID_3065394 RMVar_hsa_circ_88426,RMVar_hsa_circ_89698,RMVar_hsa_circ_125304,RMVar_hsa_circ_89605,RMVar_hsa_circ_198721,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198720 114285 RMVar_ID_114285 Human_SNP_ID_836448060 m1A Human chr2 - 218661100 218661100 218661100 TCATGTAATGGCGCCGGAATGCCACCAGGCCCAGTTGGACACCCTTCCGGGCCAGGGCCAGGGCT TCATGTAATGGCGCCGGAATGCCACCAGGCCCGGTTGGACACCCTTCCGGGCCAGGGCCAGGGCT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:218661054..218661303 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus 114286 RMVar_ID_114286 Human_SNP_ID_836508380 m1A Human chr2 - 1680269 1680269 1680269 AAAACCTACGCGGAGTCGGGGAACGCGCAGGCAGCGGCCATCTGTGAATATCCCAGACGCATCCA AAAACCTACGCGGAGTCGGGGAACGCGCAGGCTGCGGCCATCTGTGAATATCCCAGACGCATCCA T A PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1680151..1680317 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_Splice_Rec_210958,Human_Splice_Rec_210959,Human_Splice_Rec_211048,Human_Splice_Rec_211049,Human_Splice_Rec_211092,Human_Splice_Rec_211093,Human_Splice_Rec_211104,Human_Splice_Rec_211105,Human_Splice_Rec_211118 Human_miRNA_ID_708689,Human_miRNA_ID_715949,Human_miRNA_ID_1517712 RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_19997,RMVar_hsa_circ_14491,RMVar_hsa_circ_111431,RMVar_hsa_circ_196627,RMVar_hsa_circ_338685,RMVar_hsa_circ_370308,RMVar_hsa_circ_107135,RMVar_hsa_circ_196632,RMVar_hsa_circ_196633,RMVar_hsa_circ_196631,RMVar_hsa_circ_346432,RMVar_hsa_circ_349549,RMVar_hsa_circ_325190,RMVar_hsa_circ_36333,RMVar_hsa_circ_196634,RMVar_hsa_circ_74522,RMVar_hsa_circ_40790,RMVar_hsa_circ_376823,RMVar_hsa_circ_372096,RMVar_hsa_circ_196636 114287 RMVar_ID_114287 Human_SNP_ID_836536107 m1A Human chr2 - 240568905 240568905 240568905 GGGCGGCGGCGCGGGCCCCGGCCCGGGGGCGGAGAAGGCGAAGGCGCAGGGCGTCTCGGCGGCGG GGGCGGCGGCGCGGGCCCCGGCCCGGGGGCGGGGAAGGCGAAGGCGCAGGGCGTCTCGGCGGCGG T C ANKMY1 Ensembl:ENSG00000144504 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240568883..240569036 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 2 uterus Human_RBP_ID_26787517 114288 RMVar_ID_114288 Human_SNP_ID_836541672 m1A Human chr2 + 32505167 32505167 32505167 TACCATTCACCTTCCTGCAGCAGTGCTGCTTAAGGAGATACATATCCAGCCTCATCTTGCATCTC TACCATTCACCTTCCTGCAGCAGTGCTGCTTACGGAGATACATATCCAGCCTCATCTTGCATCTC A C BIRC6 Ensembl:ENSG00000115760 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:32505051..32505175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - Human_RBP_ID_205725,Human_RBP_ID_26818364 Human_Splice_Rec_233567,Human_Splice_Rec_233709 Human_miRNA_ID_1999429,Human_miRNA_ID_2147783,Human_miRNA_ID_2148582,Human_miRNA_ID_2575719,Human_miRNA_ID_2712504 RMVar_hsa_circ_16218,RMVar_hsa_circ_316322,RMVar_hsa_circ_41377,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_39974,RMVar_hsa_circ_15051,RMVar_hsa_circ_20626,RMVar_hsa_circ_25859,RMVar_hsa_circ_5923,RMVar_hsa_circ_67650,RMVar_hsa_circ_312338,RMVar_hsa_circ_51154,RMVar_hsa_circ_27815,RMVar_hsa_circ_321798,RMVar_hsa_circ_362690,RMVar_hsa_circ_67324,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_53113,RMVar_hsa_circ_393,RMVar_hsa_circ_18032,RMVar_hsa_circ_75196,RMVar_hsa_circ_43957,RMVar_hsa_circ_40702,RMVar_hsa_circ_56193,RMVar_hsa_circ_41083,RMVar_hsa_circ_317166,RMVar_hsa_circ_33306,RMVar_hsa_circ_42267,RMVar_hsa_circ_335193,RMVar_hsa_circ_288225,RMVar_hsa_circ_65955,RMVar_hsa_circ_61053,RMVar_hsa_circ_73647,RMVar_hsa_circ_339840,RMVar_hsa_circ_342878,RMVar_hsa_circ_333176,RMVar_hsa_circ_300566,RMVar_hsa_circ_276088,RMVar_hsa_circ_287224,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_75056,RMVar_hsa_circ_52062,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_106340,RMVar_hsa_circ_198489,RMVar_hsa_circ_102684,RMVar_hsa_circ_54548,RMVar_hsa_circ_64795,RMVar_hsa_circ_198493,RMVar_hsa_circ_198494,RMVar_hsa_circ_198492,RMVar_hsa_circ_340513,RMVar_hsa_circ_325095,RMVar_hsa_circ_283441,RMVar_hsa_circ_198495,RMVar_hsa_circ_198497,RMVar_hsa_circ_198496,RMVar_hsa_circ_316385,RMVar_hsa_circ_51998,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_311468,RMVar_hsa_circ_34569,RMVar_hsa_circ_315350,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_114815,RMVar_hsa_circ_111552,RMVar_hsa_circ_102726,RMVar_hsa_circ_106383,RMVar_hsa_circ_47599,RMVar_hsa_circ_28300,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,RMVar_hsa_circ_198508,RMVar_hsa_circ_198509,RMVar_hsa_circ_198506,RMVar_hsa_circ_198507,RMVar_hsa_circ_198505,RMVar_hsa_circ_198502,RMVar_hsa_circ_198503,RMVar_hsa_circ_198501,RMVar_hsa_circ_198516,RMVar_hsa_circ_79240,RMVar_hsa_circ_37960,RMVar_hsa_circ_198517,RMVar_hsa_circ_296766,RMVar_hsa_circ_315599,RMVar_hsa_circ_323044,RMVar_hsa_circ_308978,RMVar_hsa_circ_109325,RMVar_hsa_circ_285789,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_295090,RMVar_hsa_circ_366219,RMVar_hsa_circ_198519,RMVar_hsa_circ_198520,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_333302,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_283506,RMVar_hsa_circ_120631,RMVar_hsa_circ_17794,RMVar_hsa_circ_110501,RMVar_hsa_circ_116965,RMVar_hsa_circ_44304,RMVar_hsa_circ_198525,RMVar_hsa_circ_198527,RMVar_hsa_circ_198529,RMVar_hsa_circ_198530,RMVar_hsa_circ_198528,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_198535,RMVar_hsa_circ_119579,RMVar_hsa_circ_370261,RMVar_hsa_circ_198531,RMVar_hsa_circ_373647,RMVar_hsa_circ_371044,RMVar_hsa_circ_125352,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_198533,RMVar_hsa_circ_198534,RMVar_hsa_circ_322368,RMVar_hsa_circ_370824,RMVar_hsa_circ_198532,RMVar_hsa_circ_350684,RMVar_hsa_circ_273358,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_198540,RMVar_hsa_circ_198542,RMVar_hsa_circ_198543,RMVar_hsa_circ_198544,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_198537 114289 RMVar_ID_114289 Human_SNP_ID_836541856 m1A Human chr2 - 210588128 210588128 210588128 ACAAATTACTTACCTTTACTAGCAGGCGGATTACATTGTTTTTAATCCCACAGTCTACAGCTACC ACAAATTACTTACCTTTACTAGCAGGCGGATTGCATTGTTTTTAATCCCACAGTCTACAGCTACC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210588007..210588200 26863196 MeRIP-seq:(Medium) rs1308610893 Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114290 RMVar_ID_114290 Human_SNP_ID_836552100 m1A Human chr2 - 98600130 98600130 98600130 CATCATCTTCGGACTGTTTTTGTTTCCTGGTTACATTTTCAGTCTGGCCCGCTCTACATAATGGG CATCATCTTCGGACTGTTTTTGTTTCCTGGTTTCATTTTCAGTCTGGCCCGCTCTACATAATGGG T A COA5 Ensembl:ENSG00000183513 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs72823794 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2669526,Human_RBP_ID_17277380,Human_RBP_ID_22506090 GWAS_ID_8450,GWAS_ID_8451,GWAS_ID_8452,GWAS_ID_8453,GWAS_ID_8454,GWAS_ID_8455,GWAS_ID_8456,GWAS_ID_8457,GWAS_ID_8458,GWAS_ID_8459,GWAS_ID_8460,GWAS_ID_8461,GWAS_ID_8462,GWAS_ID_8463,GWAS_ID_8464,GWAS_ID_8465,GWAS_ID_8466,GWAS_ID_8467,GWAS_ID_8468,GWAS_ID_8469,GWAS_ID_8470,GWAS_ID_8471,GWAS_ID_8472,GWAS_ID_8473,GWAS_ID_8474,GWAS_ID_8475,GWAS_ID_8476,GWAS_ID_8477,GWAS_ID_8478,GWAS_ID_8479,GWAS_ID_8480,GWAS_ID_8481,GWAS_ID_8482,GWAS_ID_8483,GWAS_ID_8484,GWAS_ID_8485,GWAS_ID_8486,GWAS_ID_8487,GWAS_ID_8488,GWAS_ID_8489,GWAS_ID_8490,GWAS_ID_8491,GWAS_ID_8492,GWAS_ID_8493,GWAS_ID_8494,GWAS_ID_8495,GWAS_ID_8496,GWAS_ID_8497,GWAS_ID_8498,GWAS_ID_8499,GWAS_ID_8500,GWAS_ID_8501,GWAS_ID_8502,GWAS_ID_8503,GWAS_ID_8504,GWAS_ID_8505,GWAS_ID_8506,GWAS_ID_8507,GWAS_ID_8508,GWAS_ID_8509,GWAS_ID_8510,GWAS_ID_8511,GWAS_ID_8512,GWAS_ID_8513,GWAS_ID_8514,GWAS_ID_8515,GWAS_ID_8516,GWAS_ID_8517,GWAS_ID_8518,GWAS_ID_8519,GWAS_ID_8520,GWAS_ID_8521,GWAS_ID_8522,GWAS_ID_8523,GWAS_ID_8524,GWAS_ID_8525,GWAS_ID_8526,GWAS_ID_8527,GWAS_ID_8528,GWAS_ID_8529,GWAS_ID_8530,GWAS_ID_8531,GWAS_ID_8532,GWAS_ID_8533,GWAS_ID_8534,GWAS_ID_8535,GWAS_ID_8536,GWAS_ID_8537,GWAS_ID_8538,GWAS_ID_8539,GWAS_ID_8540,GWAS_ID_8541,GWAS_ID_8542,GWAS_ID_8543,GWAS_ID_8544,GWAS_ID_8545,GWAS_ID_8546,GWAS_ID_8547,GWAS_ID_8548,GWAS_ID_8549,GWAS_ID_8550,GWAS_ID_8551,GWAS_ID_8552,GWAS_ID_8553,GWAS_ID_8554,GWAS_ID_8555,GWAS_ID_8556,GWAS_ID_8557,GWAS_ID_8558,GWAS_ID_8559,GWAS_ID_8560,GWAS_ID_8561,GWAS_ID_8562,GWAS_ID_8563,GWAS_ID_8564,GWAS_ID_8565,GWAS_ID_8566,GWAS_ID_8567,GWAS_ID_8568,GWAS_ID_8569,GWAS_ID_8570,GWAS_ID_8571,GWAS_ID_8572,GWAS_ID_8573,GWAS_ID_8574,GWAS_ID_8575,GWAS_ID_8576,GWAS_ID_8577,GWAS_ID_8578,GWAS_ID_8579,GWAS_ID_8580,GWAS_ID_8581,GWAS_ID_8582,GWAS_ID_8583,GWAS_ID_8584,GWAS_ID_8585,GWAS_ID_8586,GWAS_ID_8587,GWAS_ID_8588,GWAS_ID_8589,GWAS_ID_8590,GWAS_ID_8591,GWAS_ID_8592,GWAS_ID_8593,GWAS_ID_8594,GWAS_ID_8595,GWAS_ID_8596,GWAS_ID_8597,GWAS_ID_8598,GWAS_ID_8599,GWAS_ID_8600,GWAS_ID_8601,GWAS_ID_8602,GWAS_ID_8603,GWAS_ID_8604,GWAS_ID_8605,GWAS_ID_8606,GWAS_ID_8607,GWAS_ID_8608,GWAS_ID_8609,GWAS_ID_8610,GWAS_ID_8611,GWAS_ID_8612,GWAS_ID_8613,GWAS_ID_8614,GWAS_ID_8615,GWAS_ID_8616,GWAS_ID_8617,GWAS_ID_8618,GWAS_ID_8619,GWAS_ID_8620,GWAS_ID_8621,GWAS_ID_8622,GWAS_ID_8623,GWAS_ID_8624,GWAS_ID_8625,GWAS_ID_8626,GWAS_ID_8627,GWAS_ID_8628,GWAS_ID_8629,GWAS_ID_8630,GWAS_ID_8631,GWAS_ID_8632,GWAS_ID_8633,GWAS_ID_8634,GWAS_ID_8635,GWAS_ID_8636,GWAS_ID_8637,GWAS_ID_8638,GWAS_ID_8639,GWAS_ID_8640,GWAS_ID_8641,GWAS_ID_8642,GWAS_ID_8643,GWAS_ID_8644,GWAS_ID_8645,GWAS_ID_8646,GWAS_ID_8647,GWAS_ID_8648,GWAS_ID_8649,GWAS_ID_8650,GWAS_ID_8651,GWAS_ID_8652,GWAS_ID_8653,GWAS_ID_8654,GWAS_ID_8655,GWAS_ID_8656,GWAS_ID_8657,GWAS_ID_8658,GWAS_ID_8659,GWAS_ID_8660,GWAS_ID_8661,GWAS_ID_8662,GWAS_ID_8663,GWAS_ID_8664,GWAS_ID_8665,GWAS_ID_8666,GWAS_ID_8667,GWAS_ID_8668,GWAS_ID_8669,GWAS_ID_8670,GWAS_ID_8671,GWAS_ID_8672,GWAS_ID_8673,GWAS_ID_8674,GWAS_ID_8675,GWAS_ID_8676,GWAS_ID_8677,GWAS_ID_8678,GWAS_ID_8679,GWAS_ID_8680,GWAS_ID_8681,GWAS_ID_8682,GWAS_ID_8683,GWAS_ID_8684,GWAS_ID_8685,GWAS_ID_8686,GWAS_ID_8687 114291 RMVar_ID_114291 Human_SNP_ID_836582096 m1A Human chr2 + 42568649 42568649 42568649 CCTCCCTTCCCCCCCGTGGCGAGGCAGCAGCGACGGCGGCGGCGGCAGCGGCGGTCGCGGCTGAG CCTCCCTTCCCCCCCGTGGCGAGGCAGCAGCGGCGGCGGCGGCGGCAGCGGCGGTCGCGGCTGAG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:42568614..42568740 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_9386417,Human_RBP_ID_18947762 RMVar_hsa_circ_199265,RMVar_hsa_circ_123561 114292 RMVar_ID_114292 Human_SNP_ID_836597418 m1A Human chr2 - 27102432 27102432 27102432 CCTCTCCCGGGCTGATTCTCCACTTTTCTGACAGACTTCTGCAGAGCTACCTAAAGGGACTAGGA CCTCTCCCGGGCTGATTCTCCACTTTTCTGACGGACTTCTGCAGAGCTACCTAAAGGGACTAGGA T C CGREF1 Ensembl:ENSG00000138028 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27102417..27102509 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LGG 1 - Human_Splice_Rec_227065,Human_Splice_Rec_227079,Human_Splice_Rec_227089,Human_Splice_Rec_227099,Human_Splice_Rec_227111,Human_Splice_Rec_227119 114293 RMVar_ID_114293 Human_SNP_ID_836634273 m1A Human chr2 - 10812664 10812664 10812664 ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCAGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCTGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT T A PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:10812662..10812775 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 6 kidney Human_RBP_ID_19103455,Human_RBP_ID_22359867,Human_RBP_ID_26786765 114294 RMVar_ID_114294 Human_SNP_ID_836634274 m1A Human chr2 - 10812664 10812664 10812664 ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCAGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT ATGGCTCTCCTGGTGCTCGGTAGGTGCGGGCCGGCGGAGGGAGGCGGGCGAGCTGGGGTCGGCCT T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:10812662..10812775 26863410 MeRIP-seq:(Medium) rs6726687 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 9 large intestine Human_RBP_ID_19103455,Human_RBP_ID_22359867,Human_RBP_ID_26786765 GWAS_ID_9300,GWAS_ID_9301,GWAS_ID_9302,GWAS_ID_9303,GWAS_ID_9304,GWAS_ID_9305,GWAS_ID_9306,GWAS_ID_9307 114295 RMVar_ID_114295 Human_SNP_ID_836649236 m1A Human chr2 + 28412054 28412045 28412055 GGCTCACGGCCCAGTGTGCAAGATTAGCCCCGAGGAGCGCCGATCGCCCCCAGCCCCTGGGCTGC GGCTCACGGCCCAGTGTGCAAGAT__________GAGCGCCGATCGCCCCCAGCCCCTGGGCTGC TTAGCCCCGAG T FOSL2 Ensembl:ENSG00000075426 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:28412001..28412200 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 25..34 33 HNSC 1 - Human_RBP_ID_917789,Human_RBP_ID_22077524 Human_miRNA_ID_1358839 RMVar_hsa_circ_198101 114296 RMVar_ID_114296 Human_SNP_ID_836652076 m1A Human chr2 + 46909176 46909176 46909176 GGGTTCTGAGCAGGGATCTCATGGTCATCAATATCTGTGAGATGGGAAACACAGAAGAGGAAGGC GGGTTCTGAGCAGGGATCTCATGGTCATCAATGTCTGTGAGATGGGAAACACAGAAGAGGAAGGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:46909080..46909217 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 11 stomach 114297 RMVar_ID_114297 Human_SNP_ID_836653557 m1A Human chr2 - 1658004 1658004 1658004 GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCAGGAGGAAGAGACAAGGAGAAAGGAAATCACAG GAGAGAGAGCCCACAGCTGAAATGGAGTGCTCCGGAGGAAGAGACAAGGAGAAAGGAAATCACAG T G PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:1657971..1658085 26863196 MeRIP-seq:(Medium) rs536446224 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 114298 RMVar_ID_114298 Human_SNP_ID_836697902 m1A Human chr2 + 54631077 54631077 54631077 GGCATGGAGCGGGACTTGGTGGCCATTGAGGCAAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA GGCATGGAGCGGGACTTGGTGGCCATTGAGGCGAAGCTGAGTGACCTGCAGAAGGAGGCGGAGAA A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:54630862..54632715 32194978 MeRIP-seq:(Medium) rs61730127 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_1919580,Human_RBP_ID_8848846 Human_miRNA_ID_2513858,Human_miRNA_ID_2513859,Human_miRNA_ID_2995912,Human_miRNA_ID_2995913 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_111082,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909 114299 RMVar_ID_114299 Human_SNP_ID_836701576 m1A Human chr2 - 241122829 241122829 241122829 GGCTGTGGAACTGGAGGGGTTGGCGGCCTGTGAGGGCGAGTACTCCCAAAAGTACAGTACCATGA GGCTGTGGAACTGGAGGGGTTGGCGGCCTGTGCGGGCGAGTACTCCCAAAAGTACAGTACCATGA T G PASK Ensembl:ENSG00000115687 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:241122734..241122907 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_22505354 Human_Splice_Rec_380666,Human_Splice_Rec_380667,Human_Splice_Rec_380700,Human_Splice_Rec_380701,Human_Splice_Rec_380740,Human_Splice_Rec_380741,Human_Splice_Rec_380774,Human_Splice_Rec_380775,Human_Splice_Rec_380818,Human_Splice_Rec_380819,Human_Splice_Rec_380828,Human_Splice_Rec_380829 RMVar_hsa_circ_15480,RMVar_hsa_circ_120120,RMVar_hsa_circ_269174,RMVar_hsa_circ_208027,RMVar_hsa_circ_118033,RMVar_hsa_circ_208026,RMVar_hsa_circ_208029,RMVar_hsa_circ_96990,RMVar_hsa_circ_98999,RMVar_hsa_circ_331132,RMVar_hsa_circ_208030 114300 RMVar_ID_114300 Human_SNP_ID_836710244 m1A Human chr2 + 214847285 214847285 214847285 CCTGCGCAGGGCCAAGTTCAAGCTTCCTGGCCACCAGAAGATCCACATCTCAAAGAAGTGGGGCT CCTGCGCAGGGCCAAGTTCAAGCTTCCTGGCCGCCAGAAGATCCACATCTCAAAGAAGTGGGGCT A G SNHG31,RPL10P6 Ensembl:ENSG00000229267,Ensembl:ENSG00000230076 lincRNA,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs928716168 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17393733 RMVar_hsa_circ_206682 114301 RMVar_ID_114301 Human_SNP_ID_836715346 m1A Human chr2 - 85595800 85595800 85595800 CATGTTGGTTCGCGTCTCCTGCTCAGGGTCCGACGGCTCGCAGTCGTGTTCATCGAAATAGGACG CATGTTGGTTCGCGTCTCCTGCTCAGGGTCCGGCGGCTCGCAGTCGTGTTCATCGAAATAGGACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85595751..85596697 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 114302 RMVar_ID_114302 Human_SNP_ID_836729087 m1A Human chr2 + 236366623 236366623 236366623 AGAAAGGGAGGGTGTGGGTGGGGTGCTTCCTGAGGGCCCTTCTGTGGTGTGTTCAAAGCCAGCTT AGAAAGGGAGGGTGTGGGTGGGGTGCTTCCTGGGGGCCCTTCTGTGGTGTGTTCAAAGCCAGCTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:236366574..236366689 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114303 RMVar_ID_114303 Human_SNP_ID_836739777 m1A Human chr2 - 232523097 232523097 232523097 GCTCTTCGGCAGGTGTCGGTGCTGAGCAGGGGAACACGGGCCTCTCTCACTGCTTCAGCCTCAGG GCTCTTCGGCAGGTGTCGGTGCTGAGCAGGGGGACACGGGCCTCTCTCACTGCTTCAGCCTCAGG T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:232522966..232523098 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - 114304 RMVar_ID_114304 Human_SNP_ID_836748363 m1A Human chr2 - 105379628 105379628 105379628 GGGCTGACGTGCCAGGTAAAAAACAGGAGCACAGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG GGGCTGACGTGCCAGGTAAAAAACAGGAGCACCGTTTAGTTTTGTCGGATCATTTCAGGTGGAAG T G FHL2 Ensembl:ENSG00000115641 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:105379626..105379773 26863196 MeRIP-seq:(Medium) rs10189100 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_202310,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305,RMVar_hsa_circ_202308,RMVar_hsa_circ_307296,RMVar_hsa_circ_86098,RMVar_hsa_circ_202311,RMVar_hsa_circ_307374 114305 RMVar_ID_114305 Human_SNP_ID_836750803 m1A Human chr2 + 3277194 3277194 3277194 AAATCCAGGAGCCTCTCCACCCACGCGGCCCCACACCTGTCTCCACCCACACGGCCCCGCACCTG AAATCCAGGAGCCTCTCCACCCACGCGGCCCCGCACCTGTCTCCACCCACACGGCCCCGCACCTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:3277190..3277305 26863196 MeRIP-seq:(Medium) rs1004892094 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114306 RMVar_ID_114306 Human_SNP_ID_836804276 m1A Human chr2 - 206141952 206141952 206141952 CCACGTTTTGAGGCACCACTGTTTAATGCTAGAATTCGAAAGAGGTTGGTAATAGTATTTATTCA CCACGTTTTGAGGCACCACTGTTTAATGCTAGGATTCGAAAGAGGTTGGTAATAGTATTTATTCA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1801318 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 15 haematopoietic and lymphoid tissue Human_RBP_ID_3958449,Human_RBP_ID_5528780 Human_Splice_Rec_349795,Human_Splice_Rec_349831,Human_Splice_Rec_349865,Human_Splice_Rec_349893,Human_Splice_Rec_349927,Human_Splice_Rec_349963,Human_Splice_Rec_349993 Clinvar_Rec_466 GWAS_ID_10611,GWAS_ID_10612,GWAS_ID_10613,GWAS_ID_10614,GWAS_ID_10615,GWAS_ID_10616 RMVar_hsa_circ_7984,RMVar_hsa_circ_97911,RMVar_hsa_circ_30382,RMVar_hsa_circ_206299,RMVar_hsa_circ_206300,RMVar_hsa_circ_276559,RMVar_hsa_circ_316144,RMVar_hsa_circ_268346,RMVar_hsa_circ_206302,RMVar_hsa_circ_206303,RMVar_hsa_circ_268452,RMVar_hsa_circ_282447,RMVar_hsa_circ_267281,RMVar_hsa_circ_268010,RMVar_hsa_circ_376770,RMVar_hsa_circ_264782,RMVar_hsa_circ_330828,RMVar_hsa_circ_305902,RMVar_hsa_circ_306855,RMVar_hsa_circ_280997,RMVar_hsa_circ_281500,RMVar_hsa_circ_206304,RMVar_hsa_circ_206308,RMVar_hsa_circ_206310,RMVar_hsa_circ_206309,RMVar_hsa_circ_206306,RMVar_hsa_circ_206307,RMVar_hsa_circ_206305,RMVar_hsa_circ_275402,RMVar_hsa_circ_206315,RMVar_hsa_circ_267152,RMVar_hsa_circ_312695,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_337316,RMVar_hsa_circ_307994,RMVar_hsa_circ_322160,RMVar_hsa_circ_298623,RMVar_hsa_circ_206317,RMVar_hsa_circ_206319,RMVar_hsa_circ_206320,RMVar_hsa_circ_206318,RMVar_hsa_circ_288831,RMVar_hsa_circ_325030,RMVar_hsa_circ_370066,RMVar_hsa_circ_206316,RMVar_hsa_circ_330250,RMVar_hsa_circ_323363,RMVar_hsa_circ_71448,RMVar_hsa_circ_283055,RMVar_hsa_circ_50273,RMVar_hsa_circ_206329,RMVar_hsa_circ_292208,RMVar_hsa_circ_362125,RMVar_hsa_circ_206322,RMVar_hsa_circ_206324,RMVar_hsa_circ_206325,RMVar_hsa_circ_206323,RMVar_hsa_circ_206321,RMVar_hsa_circ_378442,RMVar_hsa_circ_309096,RMVar_hsa_circ_357000,RMVar_hsa_circ_306634,RMVar_hsa_circ_206331,RMVar_hsa_circ_287242,RMVar_hsa_circ_206330,RMVar_hsa_circ_206327,RMVar_hsa_circ_206328,RMVar_hsa_circ_206326 114307 RMVar_ID_114307 Human_SNP_ID_836812734 m1A Human chr2 + 27242719 27242719 27242719 ATCGTGTCAGCCTGCGCTACGTGGCACCTCCCAGCCTGCGCATGCCACCCACTGTGCGGGCCTTC ATCGTGTCAGCCTGCGCTACGTGGCACCTCCCCGCCTGCGCATGCCACCCACTGTGCGGGCCTTC A C CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27242618..27242725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_Splice_Rec_227626,Human_Splice_Rec_227627,Human_Splice_Rec_227710,Human_Splice_Rec_227711,Human_Splice_Rec_227772 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_197946,RMVar_hsa_circ_86946,RMVar_hsa_circ_117636,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_119126,RMVar_hsa_circ_197954,RMVar_hsa_circ_197955,RMVar_hsa_circ_197956,RMVar_hsa_circ_197961,RMVar_hsa_circ_197959,RMVar_hsa_circ_79794,RMVar_hsa_circ_113406,RMVar_hsa_circ_123806,RMVar_hsa_circ_197966,RMVar_hsa_circ_124668,RMVar_hsa_circ_197967,RMVar_hsa_circ_197968,RMVar_hsa_circ_75906,RMVar_hsa_circ_16189,RMVar_hsa_circ_370922,RMVar_hsa_circ_197969 114308 RMVar_ID_114308 Human_SNP_ID_836851790 m1A Human chr2 + 231712956 231712956 231712956 CAGAATCTAAACGTGGTCACCTTCGAGTAGAGAGGCCCGCCCGCCCACCGTGGGCAGTGCCACCC CAGAATCTAAACGTGGTCACCTTCGAGTAGAGGGGCCCGCCCGCCCACCGTGGGCAGTGCCACCC A G PTMA Ensembl:ENSG00000187514 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr2:231712801..231713025;chr2:231712076..231713025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SARC 2 - Human_RBP_ID_243210,Human_RBP_ID_545774,Human_RBP_ID_774376,Human_RBP_ID_920686,Human_RBP_ID_4599558,Human_RBP_ID_5147746,Human_RBP_ID_8200838,Human_RBP_ID_9103880,Human_RBP_ID_9385687,Human_RBP_ID_17280112,Human_RBP_ID_17509838,Human_RBP_ID_17658755,Human_RBP_ID_17952237,Human_RBP_ID_22248661,Human_RBP_ID_23856736,Human_RBP_ID_26487696,Human_RBP_ID_27007857 Human_miRNA_ID_2872614,Human_miRNA_ID_2980581 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 114309 RMVar_ID_114309 Human_SNP_ID_836885570 m1A Human chr2 - 241256204 241256204 241256204 AGGAACAGTTGGCTCAGGCTGTGGCTCGCATCAAGAAGATTTATGAGGAGAAGGTACACGATTTA AGGAACAGTTGGCTCAGGCTGTGGCTCGCATCCAGAAGATTTATGAGGAGAAGGTACACGATTTA T G HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:241256201..241256225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_242530,Human_RBP_ID_547016,Human_RBP_ID_829688,Human_RBP_ID_922588,Human_RBP_ID_6900800,Human_RBP_ID_8847022,Human_RBP_ID_9385898,Human_RBP_ID_13821379,Human_RBP_ID_17506756,Human_RBP_ID_18443317,Human_RBP_ID_22998893,Human_RBP_ID_24546274,Human_RBP_ID_26338896,Human_RBP_ID_27818154 Human_Splice_Rec_381269,Human_Splice_Rec_381323,Human_Splice_Rec_381379,Human_Splice_Rec_381431,Human_Splice_Rec_381503,Human_Splice_Rec_381631,Human_Splice_Rec_381645 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_78553,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_63419,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_375899,RMVar_hsa_circ_279198,RMVar_hsa_circ_371246,RMVar_hsa_circ_208089,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_302446,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_208092,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_20829 114310 RMVar_ID_114310 Human_SNP_ID_836914150 m1A Human chr2 + 214847503 214847502 214847503 TTAATACTCACCAATAAATTCTACTTCCTGTCAAAAAAATGTCACTAATGTACCCTAAATTTTCT TTAATACTCACCAATAAATTCTACTTCCTGTC_AAAAAATGTCACTAATGTACCCTAAATTTTCT CA C SNHG31 Ensembl:ENSG00000229267 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1448274769 Functional Loss DEL ICGC 33..33 33 ESCA 2 - Human_RBP_ID_543850,Human_RBP_ID_1240885,Human_RBP_ID_3615403,Human_RBP_ID_26488197 RMVar_hsa_circ_206682 114311 RMVar_ID_114311 Human_SNP_ID_836937708 m1A Human chr2 + 197498847 197498847 197498847 TCATCTGGCGAAAGACTGTGGGTAACCGAAGCATTTCTGGGGATGGAAGCAAAAAGATCATCAGA TCATCTGGCGAAAGACTGTGGGTAACCGAAGCGTTTCTGGGGATGGAAGCAAAAAGATCATCAGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:197498625..197498897;chr2:197498745..197498892 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NKTL 1 - 114312 RMVar_ID_114312 Human_SNP_ID_836945591 m1A Human chr2 + 96191505 96191505 96191505 GTTTTCGAGTACCCTCTGTACACAGTCAATGCAATTTATCACTTCTCCCTAACCTCTACTTTCCT GTTTTCGAGTACCCTCTGTACACAGTCAATGCGATTTATCACTTCTCCCTAACCTCTACTTTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96191502..96191598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114313 RMVar_ID_114313 Human_SNP_ID_836982947 m1A Human chr2 - 28908038 28908038 28908038 ACTTACCATCCTACAACCAGATTACAGTAACAATCTATCTGCCTTCTCTGCCTTTAACTAGCTCC ACTTACCATCCTACAACCAGATTACAGTAACACTCTATCTGCCTTCTCTGCCTTTAACTAGCTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:28908035..28908124 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 114314 RMVar_ID_114314 Human_SNP_ID_836996874 m1A Human chr2 - 55544365 55544365 55544365 AATCTTGACATATTAAGGCTAGCCATACCTCTACCTCCCCAGTGGGTTTTCCTTTCTGCTCCATA AATCTTGACATATTAAGGCTAGCCATACCTCTGCCTCCCCAGTGGGTTTTCCTTTCTGCTCCATA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:55544315..55544399 26863196 MeRIP-seq:(Medium) rs1196311266 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung 114315 RMVar_ID_114315 Human_SNP_ID_837026698 m1A Human chr2 - 84428080 84428080 84428080 GAGCTAGAGCATTCTGGGGTTACTGGAAGATAAGGAGAAAGGGAGGAAAGGTGGCAGATGAGGCA GAGCTAGAGCATTCTGGGGTTACTGGAAGATAGGGAGAAAGGGAGGAAAGGTGGCAGATGAGGCA T C SUCLG1 Ensembl:ENSG00000163541 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:84428072..84428186 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_79116,RMVar_hsa_circ_110153,RMVar_hsa_circ_115801,RMVar_hsa_circ_20573,RMVar_hsa_circ_201482,RMVar_hsa_circ_201483,RMVar_hsa_circ_201481,RMVar_hsa_circ_346539,RMVar_hsa_circ_359222,RMVar_hsa_circ_91999,RMVar_hsa_circ_201484 114316 RMVar_ID_114316 Human_SNP_ID_837038993 m1A Human chr2 - 240596808 240596808 240596808 CGAGAAGGGGAAGCAGGGGTTGGTGGGGTATGAGGCAAAGTTCCTGCTGCCCCCCGCCGTCTGGC CGAGAAGGGGAAGCAGGGGTTGGTGGGGTATGTGGCAAAGTTCCTGCTGCCCCCCGCCGTCTGGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240596759..240598017 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 114317 RMVar_ID_114317 Human_SNP_ID_837047810 m1A Human chr2 - 96143902 96143902 96143902 GCGGCTGGACGAGGCCTTTGACTTCGTTAAGCAGCGCCGGGGGGTCATCTCCCCCAACTTCAGTT GCGGCTGGACGAGGCCTTTGACTTCGTTAAGCCGCGCCGGGGGGTCATCTCCCCCAACTTCAGTT T G DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:96143851..96143925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_miRNA_ID_2064381,Human_miRNA_ID_2933561 RMVar_hsa_circ_94669,RMVar_hsa_circ_201829 114318 RMVar_ID_114318 Human_SNP_ID_837059606 m1A Human chr2 - 27441838 27441838 27441838 GGCTGCAGCACGTCCAGGGACAGCCACAGCGCAGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG GGCTGCAGCACGTCCAGGGACAGCCACAGCGCTGATCAGGGCCTGGCCCGAGTGAGCTCTAAGAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27441710..27442209 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 114319 RMVar_ID_114319 Human_SNP_ID_837066617 m1A Human chr2 - 27225884 27225850 27225885 TTGCCATAGGCGTCTCTCACCACCTCGTACTCAATCTCCTTCCATCCCTTCAGAGACTTGTCTAC TTGCCATAGGCGTCTCTCACCACCTCGTACT__________________________________ TAGTAGACAAGTCTCTGAAGGGATGGAAGGAGATTG T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27225834..27225952 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..65 33 PAAD 1 - 114320 RMVar_ID_114320 Human_SNP_ID_837072097 m1A Human chr2 - 144389659 144389659 144389659 GAGCGAGAAGGAGCACGAGAAAGAAGGCGAGGATGGCTACGGGAAGCTGGGCAGACAGGATGGCG GAGCGAGAAGGAGCACGAGAAAGAAGGCGAGGTTGGCTACGGGAAGCTGGGCAGACAGGATGGCG T A ZEB2 Ensembl:ENSG00000169554 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:144389608..144389715 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 14 skin,head and neck Human_RBP_ID_24545862 Human_Splice_Rec_302096 114321 RMVar_ID_114321 Human_SNP_ID_837090065 m1A Human chr2 + 97646130 97646130 97646130 GTTACTTCGCGGAGCTGGAACGCTGGCCGCGCAGGCCCTGAGGGCTCGCGGCCCCAGTGGCGCGG GTTACTTCGCGGAGCTGGAACGCTGGCCGCGCGGGCCCTGAGGGCTCGCGGCCCCAGTGGCGCGG A G COX5B Ensembl:ENSG00000135940 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:97646076..97646150;chr2:97646126..97646150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_558392,Human_RBP_ID_1591985,Human_RBP_ID_4621602,Human_RBP_ID_5118002,Human_RBP_ID_5146617,Human_RBP_ID_5322164,Human_RBP_ID_9330598,Human_RBP_ID_17657455,Human_RBP_ID_18422692,Human_RBP_ID_22449943,Human_RBP_ID_23212061,Human_RBP_ID_26770378,Human_RBP_ID_26818799 Human_Splice_Rec_277887,Human_Splice_Rec_277893 Human_miRNA_ID_2352740,Human_miRNA_ID_2572124 RMVar_hsa_circ_82754,RMVar_hsa_circ_268030,RMVar_hsa_circ_201980 114322 RMVar_ID_114322 Human_SNP_ID_837092206 m1A Human chr2 - 171922509 171922509 171922509 TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTACCCGCCATTTCCGAGCTACGATCACCCGCGGC TCCTCCCCTTGGTAAACTTTTCCCGGTAACTTGCCCGCCATTTCCGAGCTACGATCACCCGCGGC T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:171922465..171922560;chr2:171922426..171922647;chr2:171922479..171922581 26863196 MeRIP-seq:(Medium) rs76979357 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 114323 RMVar_ID_114323 Human_SNP_ID_837099637 m1A Human chr2 + 27037701 27037701 27037701 CACCCCTAGCTGTCCCCCTGAGATGAAGAAAGAGGTGAGGATATGGTGGGAGGCTTTTTCTCCTT CACCCCTAGCTGTCCCCCTGAGATGAAGAAAGTGGTGAGGATATGGTGGGAGGCTTTTTCTCCTT A T TMEM214 Ensembl:ENSG00000119777 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:27037676..27037725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_Splice_Rec_226661,Human_Splice_Rec_226693,Human_Splice_Rec_226723,Human_Splice_Rec_226751,Human_Splice_Rec_226781 RMVar_hsa_circ_315911,RMVar_hsa_circ_107517,RMVar_hsa_circ_40928,RMVar_hsa_circ_61860,RMVar_hsa_circ_197841,RMVar_hsa_circ_197840,RMVar_hsa_circ_76788,RMVar_hsa_circ_94383,RMVar_hsa_circ_197846,RMVar_hsa_circ_72976,RMVar_hsa_circ_197845,RMVar_hsa_circ_113408,RMVar_hsa_circ_121855,RMVar_hsa_circ_79068,RMVar_hsa_circ_122109,RMVar_hsa_circ_197847,RMVar_hsa_circ_266054,RMVar_hsa_circ_197848,RMVar_hsa_circ_121339,RMVar_hsa_circ_103260,RMVar_hsa_circ_197849,RMVar_hsa_circ_197850,RMVar_hsa_circ_104767,RMVar_hsa_circ_197851,RMVar_hsa_circ_197852,RMVar_hsa_circ_341214,RMVar_hsa_circ_197854,RMVar_hsa_circ_197856,RMVar_hsa_circ_110063,RMVar_hsa_circ_375240,RMVar_hsa_circ_197855 114324 RMVar_ID_114324 Human_SNP_ID_837108377 m1A Human chr2 + 38482059 38482059 38482059 CATGATGCGCAAGGCCATCCGAGGGCACCTGGAAAACAACCCAGCTCTGGAGAAACTGCTGCCTC CATGATGCGCAAGGCCATCCGAGGGCACCTGGGAAACAACCCAGCTCTGGAGAAACTGCTGCCTC A G RPLP0P6 Ensembl:ENSG00000213553 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_550620,Human_RBP_ID_1064024,Human_RBP_ID_5295132,Human_RBP_ID_5652085,Human_RBP_ID_8203224,Human_RBP_ID_9113848,Human_RBP_ID_17393175,Human_RBP_ID_17618270,Human_RBP_ID_17699901,Human_RBP_ID_18193275,Human_RBP_ID_19105649,Human_RBP_ID_22425693,Human_RBP_ID_26818381 Human_miRNA_ID_1889810,Human_miRNA_ID_1891991 114325 RMVar_ID_114325 Human_SNP_ID_837116924 m1A Human chr2 + 54657961 54657961 54657961 CCGAGAGATAGGCCAGAGCGTGGACGAGGTGGAGAAGCTCATCAAGCGCCACGAGGCATTTGAAA CCGAGAGATAGGCCAGAGCGTGGACGAGGTGGCGAAGCTCATCAAGCGCCACGAGGCATTTGAAA A C SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:54657851..54658025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_242450,Human_RBP_ID_775103,Human_RBP_ID_920050,Human_RBP_ID_8848920,Human_RBP_ID_9108548,Human_RBP_ID_9297249,Human_RBP_ID_9383774,Human_RBP_ID_17699273,Human_RBP_ID_22451272,Human_RBP_ID_24377424 Human_Splice_Rec_245805,Human_Splice_Rec_245871,Human_Splice_Rec_245963,Human_Splice_Rec_245973 Human_miRNA_ID_2893377,Human_miRNA_ID_2893378 RMVar_hsa_circ_111082,RMVar_hsa_circ_114144,RMVar_hsa_circ_199897,RMVar_hsa_circ_117396,RMVar_hsa_circ_199903,RMVar_hsa_circ_92406,RMVar_hsa_circ_199904,RMVar_hsa_circ_87751,RMVar_hsa_circ_76233,RMVar_hsa_circ_199906,RMVar_hsa_circ_127836,RMVar_hsa_circ_199909,RMVar_hsa_circ_108118,RMVar_hsa_circ_199911,RMVar_hsa_circ_199913,RMVar_hsa_circ_89840,RMVar_hsa_circ_199912,RMVar_hsa_circ_87065,RMVar_hsa_circ_120259,RMVar_hsa_circ_199914,RMVar_hsa_circ_92733,RMVar_hsa_circ_100796,RMVar_hsa_circ_199916,RMVar_hsa_circ_77244,RMVar_hsa_circ_97546,RMVar_hsa_circ_199917,RMVar_hsa_circ_199918,RMVar_hsa_circ_199919,RMVar_hsa_circ_113664,RMVar_hsa_circ_80058,RMVar_hsa_circ_199922,RMVar_hsa_circ_199923,RMVar_hsa_circ_199921,RMVar_hsa_circ_90114,RMVar_hsa_circ_85457,RMVar_hsa_circ_199925,RMVar_hsa_circ_199926,RMVar_hsa_circ_120851,RMVar_hsa_circ_199927,RMVar_hsa_circ_326303,RMVar_hsa_circ_199928 114326 RMVar_ID_114326 Human_SNP_ID_837169433 m1A Human chr2 + 1658248 1658248 1658248 CTGTGTGGTTCCACTTCACGCTGTTGTCTTCAAATTTACACCATCGTCCTGACCTCTCCCTGCAG CTGTGTGGTTCCACTTCACGCTGTTGTCTTCACATTTACACCATCGTCCTGACCTCTCCCTGCAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:1658245..1658497 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114327 RMVar_ID_114327 Human_SNP_ID_837192949 m1A Human chr2 + 73112455 73112455 73112455 CGATGAGCGAGCGGTGCATGGTGGTGAGCACCAGCTCGCAGGCGGCGGCGGAGCTCGCGGCCCAG CGATGAGCGAGCGGTGCATGGTGGTGAGCACCGGCTCGCAGGCGGCGGCGGAGCTCGCGGCCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:73112405..73112854 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 114328 RMVar_ID_114328 Human_SNP_ID_837216342 m1A Human chr2 + 200472952 200472952 200472952 ACAGAGTAACTTTTCCCGAAAATCATCCACTCACAATAAGCCCTCTGAAGGCAAAGCGGCAAACC ACAGAGTAACTTTTCCCGAAAATCATCCACTCTCAATAAGCCCTCTGAAGGCAAAGCGGCAAACC A T SPATS2L Ensembl:ENSG00000196141 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:200472902..200473087 26863196 MeRIP-seq:(Medium) rs1228688147 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 11 stomach Human_RBP_ID_8106443,Human_RBP_ID_9385292,Human_RBP_ID_17280028,Human_RBP_ID_21931119 Human_Splice_Rec_343757 RMVar_hsa_circ_107541,RMVar_hsa_circ_205787,RMVar_hsa_circ_32393 114329 RMVar_ID_114329 Human_SNP_ID_837216347 m1A Human chr2 + 200472952 200472952 200472952 ACAGAGTAACTTTTCCCGAAAATCATCCACTCACAATAAGCCCTCTGAAGGCAAAGCGGCAAACC ACAGAGTAACTTTTCCCGAAAATCATCCACTCGCAATAAGCCCTCTGAAGGCAAAGCGGCAAACC A G SPATS2L Ensembl:ENSG00000196141 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:200472902..200473087 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 10 stomach Human_RBP_ID_8106443,Human_RBP_ID_9385292,Human_RBP_ID_17280028,Human_RBP_ID_21931119 Human_Splice_Rec_343757 RMVar_hsa_circ_107541,RMVar_hsa_circ_205787,RMVar_hsa_circ_32393 114330 RMVar_ID_114330 Human_SNP_ID_837256510 m1A Human chr2 - 202034769 202034769 202034769 TGGGCTGGCAGAAGCCGTGGTCCGGCACGGAGATGCCCTTCTCTCCGTGGTACGGCTGCGCCCCG TGGGCTGGCAGAAGCCGTGGTCCGGCACGGAGTTGCCCTTCTCTCCGTGGTACGGCTGCGCCCCG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:202034685..202034983 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114331 RMVar_ID_114331 Human_SNP_ID_837264707 m1A Human chr2 - 87348787 87348787 87348787 GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCGGC GGAGAGGCGGACAGCGGCGGCGCGGCGGAGAGGCGGACAGCGGCGGAGAGGCAGACAGCGGCGGC T C lnc-PLGLB1-6 RNACentral:URS0000D5E001 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:87348709..87348851;chr2:87348725..87348850;chr2:87348718..87348960;chr2:87348714..87348850 26863196 MeRIP-seq:(Medium) rs62145313 Functional Loss SNV ICGC 33..33 33 LICA 1 - 114332 RMVar_ID_114332 Human_SNP_ID_837264925 m1A Human chr2 + 96740017 96740017 96740017 GACAAACATCGCCGCCACTGCTGCCACGACCCAAGGGGTCCCAGAGTCGCCGCCATCTTTCCCAC GACAAACATCGCCGCCACTGCTGCCACGACCCTAGGGGTCCCAGAGTCGCCGCCATCTTTCCCAC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:96739819..96740050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung 114333 RMVar_ID_114333 Human_SNP_ID_837292229 m1A Human chr2 - 215312549 215312549 215312549 CGGAAGCGACCAGATTCAAACCAAGAGCGGTCAGGTTTCTTGCAAATTCCACAAGGCCGGTTTTG CGGAAGCGACCAGATTCAAACCAAGAGCGGTCGGGTTTCTTGCAAATTCCACAAGGCCGGTTTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:215312476..215312575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114334 RMVar_ID_114334 Human_SNP_ID_837326673 m1A Human chr2 - 176130473 176130473 176130473 CGGCGGCGTGACGGCCGCCGACCTCGGGCGCGAAGTGACAGTCGTAGTAAGTGGGATTGATGGCC CGGCGGCGTGACGGCCGCCGACCTCGGGCGCGGAGTGACAGTCGTAGTAAGTGGGATTGATGGCC T C HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176130423..176130834 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114335 RMVar_ID_114335 Human_SNP_ID_837381014 m1A Human chr2 - 215430749 215430749 215430749 GGCTGGATGATGGTAGATTGTACTTGCCTGGGAGAAGGCAGCGGACGCATCACTTGCACTTCTAG GGCTGGATGATGGTAGATTGTACTTGCCTGGGTGAAGGCAGCGGACGCATCACTTGCACTTCTAG T A FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:215430726..215430800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 13 kidney Human_RBP_ID_242475,Human_RBP_ID_775194,Human_RBP_ID_828403,Human_RBP_ID_923466,Human_RBP_ID_17698397,Human_RBP_ID_17965017,Human_RBP_ID_22450797,Human_RBP_ID_22765598 Human_Splice_Rec_355035,Human_Splice_Rec_355123,Human_Splice_Rec_355213,Human_Splice_Rec_355305,Human_Splice_Rec_355395,Human_Splice_Rec_355481,Human_Splice_Rec_355605,Human_Splice_Rec_355695,Human_Splice_Rec_355783,Human_Splice_Rec_355873,Human_Splice_Rec_356051 RMVar_hsa_circ_63624,RMVar_hsa_circ_122684,RMVar_hsa_circ_206723,RMVar_hsa_circ_53921,RMVar_hsa_circ_380,RMVar_hsa_circ_93135,RMVar_hsa_circ_206728,RMVar_hsa_circ_23850,RMVar_hsa_circ_112126,RMVar_hsa_circ_206738,RMVar_hsa_circ_62665,RMVar_hsa_circ_269134,RMVar_hsa_circ_266791,RMVar_hsa_circ_116298,RMVar_hsa_circ_206745,RMVar_hsa_circ_61971,RMVar_hsa_circ_358981,RMVar_hsa_circ_53859,RMVar_hsa_circ_364741,RMVar_hsa_circ_298619,RMVar_hsa_circ_88129,RMVar_hsa_circ_206757,RMVar_hsa_circ_102528,RMVar_hsa_circ_59687,RMVar_hsa_circ_87667,RMVar_hsa_circ_206763,RMVar_hsa_circ_206764,RMVar_hsa_circ_357312,RMVar_hsa_circ_79733,RMVar_hsa_circ_97118,RMVar_hsa_circ_374731,RMVar_hsa_circ_81939,RMVar_hsa_circ_206773,RMVar_hsa_circ_206774,RMVar_hsa_circ_206775,RMVar_hsa_circ_206772,RMVar_hsa_circ_60002,RMVar_hsa_circ_347100,RMVar_hsa_circ_305095,RMVar_hsa_circ_45538,RMVar_hsa_circ_352311,RMVar_hsa_circ_101606,RMVar_hsa_circ_206785,RMVar_hsa_circ_356934,RMVar_hsa_circ_375702,RMVar_hsa_circ_338351,RMVar_hsa_circ_206788,RMVar_hsa_circ_206789,RMVar_hsa_circ_102369,RMVar_hsa_circ_351390,RMVar_hsa_circ_61155,RMVar_hsa_circ_63447,RMVar_hsa_circ_317301,RMVar_hsa_circ_352093,RMVar_hsa_circ_206791,RMVar_hsa_circ_330775,RMVar_hsa_circ_206792,RMVar_hsa_circ_350186,RMVar_hsa_circ_61922,RMVar_hsa_circ_73915,RMVar_hsa_circ_364012,RMVar_hsa_circ_58013 114336 RMVar_ID_114336 Human_SNP_ID_837385857 m1A Human chr2 - 201085507 201085507 201085507 CCCCATTTGAATCCTTTAAAGAATACATCAGAAAAGGAAACACTCTTTGCAAAGCCACCCATGTA CCCCATTTGAATCCTTTAAAGAATACATCAGATAAGGAAACACTCTTTGCAAAGCCACCCATGTA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:201078930..201085558 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114337 RMVar_ID_114337 Human_SNP_ID_837390297 m1A Human chr2 - 112138732 112138732 112138732 CACTGGCCTGGAGAGAGGCGGGAGGGACACTGACCTGGGAAGCCCGCGGCTCGGGGCAGGCGAGG CACTGGCCTGGAGAGAGGCGGGAGGGACACTGGCCTGGGAAGCCCGCGGCTCGGGGCAGGCGAGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:112138719..112138950 26863196 MeRIP-seq:(Medium) rs1217247969 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500 114338 RMVar_ID_114338 Human_SNP_ID_837428087 m1A Human chr2 + 240594044 240594044 240594044 GGGCCGGCGGTGCTGGCAGGGGCTCTGGAGAGAGGGGTGAGTGCTGGGGCCTGGACCATGCTGCT GGGCCGGCGGTGCTGGCAGGGGCTCTGGAGAGGGGGGTGAGTGCTGGGGCCTGGACCATGCTGCT A G CAPN10 Ensembl:ENSG00000142330 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:240593863..240594264 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_5382359 Human_Splice_Rec_378215,Human_Splice_Rec_378235,Human_Splice_Rec_378265,Human_Splice_Rec_378285,Human_Splice_Rec_378307,Human_Splice_Rec_378325,Human_Splice_Rec_378345,Human_Splice_Rec_378359 RMVar_hsa_circ_103084,RMVar_hsa_circ_207984 114339 RMVar_ID_114339 Human_SNP_ID_837439768 m1A Human chr2 + 38377209 38377209 38377209 GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCACAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG GGCGCTTGGGTCGCTGGTCCGTCGCCGGCGCCGCAGCCCCTGGTGCGGTTGCTGCCCTCGCGCTG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:38377097..38377275 26863196 MeRIP-seq:(Medium) rs3731847 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,liver hepatocellular_carcinoma 5 liver 114340 RMVar_ID_114340 Human_SNP_ID_837446593 m1A Human chr2 + 65266607 65266607 65266607 GAGAAATGATAGGATCTGATGTATATTTTTAAAGGATCATTAAGTCTGGTGTGGTGAATAGACTC GAGAAATGATAGGATCTGATGTATATTTTTAACGGATCATTAAGTCTGGTGTGGTGAATAGACTC A C ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:65266605..65266751 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_81109,RMVar_hsa_circ_200786 114341 RMVar_ID_114341 Human_SNP_ID_837448028 m1A Human chr2 - 10427040 10427040 10427040 ACTTGAACCCTGCATGTCACCACATCCCTGGGAGTTGCCCTGGAAGGGACCGGGCCAGGCGTGAG ACTTGAACCCTGCATGTCACCACATCCCTGGGGGTTGCCCTGGAAGGGACCGGGCCAGGCGTGAG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:10427026..10427050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 6 breast 114342 RMVar_ID_114342 Human_SNP_ID_837450115 m1A Human chr2 + 240465580 240465580 240465580 GCCGGACATGACCATCCGGCAGCAGATCATGCAGCTGAAGATCATGACCAACCGGCTGCGCAGCG GCCGGACATGACCATCCGGCAGCAGATCATGCGGCTGAAGATCATGACCAACCGGCTGCGCAGCG A G GPC1 Ensembl:ENSG00000063660 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:240465529..240465630 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_56233 Human_Splice_Rec_377729,Human_Splice_Rec_377743,Human_Splice_Rec_377757,Human_Splice_Rec_377787,Human_Splice_Rec_377797,Human_Splice_Rec_377799 Human_miRNA_ID_2616982 RMVar_hsa_circ_13927,RMVar_hsa_circ_80045,RMVar_hsa_circ_81970,RMVar_hsa_circ_207953,RMVar_hsa_circ_207955,RMVar_hsa_circ_207954,RMVar_hsa_circ_101314,RMVar_hsa_circ_80551,RMVar_hsa_circ_91872,RMVar_hsa_circ_207958,RMVar_hsa_circ_207959,RMVar_hsa_circ_97619,RMVar_hsa_circ_207960,RMVar_hsa_circ_91453,RMVar_hsa_circ_207961,RMVar_hsa_circ_207962 114343 RMVar_ID_114343 Human_SNP_ID_837455033 m1A Human chr2 + 74460282 74460281 74460282 TACGAGGATGTGGTTCACCGCCCAGGCACACCACCCCCCCCTTATACTGTGGCCCCAGGCCGCCC TACGAGGATGTGGTTCACCGCCCAGGCACACC_CCCCCCCCTTATACTGTGGCCCCAGGCCGCCC CA C WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74460236..74460417 26863196 MeRIP-seq:(Medium) rs1433815904 Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_555931,Human_RBP_ID_27481867,Human_RBP_ID_27564077 Human_Splice_Rec_264918,Human_Splice_Rec_264932,Human_Splice_Rec_264940,Human_Splice_Rec_264946,Human_Splice_Rec_264960,Human_Splice_Rec_264968,Human_Splice_Rec_264974,Human_Splice_Rec_264980,Human_Splice_Rec_264986,Human_Splice_Rec_264994,Human_Splice_Rec_265002,Human_Splice_Rec_265018 114344 RMVar_ID_114344 Human_SNP_ID_837485812 m1A Human chr2 - 24793240 24793225 24793240 TCACAAGCTCCGTTCTCCTGGCCGGCGGGCGCACTGGTAGCGCAGGCTTGTCACGCGGCCACCGC TCACAAGCTCCGTTCTCCTGGCCGGCGGGCGC_______________TTGTCACGCGGCCACCGC AGCCTGCGCTACCAGT A PTRHD1 Ensembl:ENSG00000184924 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr2:24793151..24793350;chr2:24793201..24793250 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..47 33 BRCA 1 - Human_RBP_ID_4623150,Human_RBP_ID_17954247,Human_RBP_ID_26818254 114345 RMVar_ID_114345 Human_SNP_ID_837516767 m1A Human chr2 - 9305277 9305277 9305277 CCCACTACTACAGCCTCTACACCAACATCTATACCCCACTATTACAGCCCCTCCACCAATATGTA CCCACTACTACAGCCTCTACACCAACATCTATCCCCCACTATTACAGCCCCTCCACCAATATGTA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:9304780..9305534 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114346 RMVar_ID_114346 Human_SNP_ID_837530501 m1A Human chr2 + 95384206 95384204 95384206 ACACACACACACACACACACACACACACACACAGCCATTCATCTGGGCTGGCAGAGGGGACAGAG ACACACACACACACACACACACACACACACA__GCCATTCATCTGGGCTGGCAGAGGGGACAGAG ACA A KCNIP3 Ensembl:ENSG00000115041 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:95384158..95384225 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 LMS 1 - 114347 RMVar_ID_114347 Human_SNP_ID_837544068 m1A Human chr2 + 174395816 174395816 174395816 GTCCACCTGTCACTTCGGGTAGCTGGGAGGCCAGGTGAGGGGCGCGCACGGGGGAGGGGCGTGCA GTCCACCTGTCACTTCGGGTAGCTGGGAGGCCGGGTGAGGGGCGCGCACGGGGGAGGGGCGTGCA A G SCRN3 Ensembl:ENSG00000144306 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:174395772..174395927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4623725 Human_Splice_Rec_325335,Human_Splice_Rec_325347,Human_Splice_Rec_325359,Human_Splice_Rec_325373,Human_Splice_Rec_325383,Human_Splice_Rec_325393 114348 RMVar_ID_114348 Human_SNP_ID_837550349 m1A Human chr2 - 69437393 69437393 69437393 AAGATGGCGGCGACGGCCAGGCGGGGCTGGGGAGCTGCGGCTGTTGCCGCCGGGCTGCGCAGGCG AAGATGGCGGCGACGGCCAGGCGGGGCTGGGGGGCTGCGGCTGTTGCCGCCGGGCTGCGCAGGCG T C NFU1 Ensembl:ENSG00000169599 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:69437289..69437396 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_243903,Human_RBP_ID_4623365,Human_RBP_ID_9330491,Human_RBP_ID_17392681 Human_Splice_Rec_255847,Human_Splice_Rec_255887,Human_Splice_Rec_255901,Human_Splice_Rec_255921,Human_Splice_Rec_255933 114349 RMVar_ID_114349 Human_SNP_ID_837580840 m1A Human chr2 - 27372728 27372728 27372728 AGTTTCCTGCAACCACTCACCAGCTTGCATGTACTTCTCTAACTGCTCTCTCCTCTGTTCTACCT AGTTTCCTGCAACCACTCACCAGCTTGCATGTCCTTCTCTAACTGCTCTCTCCTCTGTTCTACCT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27372677..27372781 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114350 RMVar_ID_114350 Human_SNP_ID_837658625 m1A Human chr2 - 55922410 55922410 55922410 CAATGTTGAAAGCCCTTTTCCTAACTATGCTGACTCTGGCGCTGGTCAAGTCACAGGACACCGAA CAATGTTGAAAGCCCTTTTCCTAACTATGCTGGCTCTGGCGCTGGTCAAGTCACAGGACACCGAA T C EFEMP1 Ensembl:ENSG00000115380 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55922313..55922481 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_57337,Human_RBP_ID_2653284,Human_RBP_ID_8521820,Human_RBP_ID_27158633,Human_RBP_ID_27480772 Human_Splice_Rec_248960,Human_Splice_Rec_248961,Human_Splice_Rec_248980,Human_Splice_Rec_248981,Human_Splice_Rec_249000,Human_Splice_Rec_249001,Human_Splice_Rec_249028,Human_Splice_Rec_249029,Human_Splice_Rec_249034,Human_Splice_Rec_249035,Human_Splice_Rec_249044,Human_Splice_Rec_249045,Human_Splice_Rec_249054,Human_Splice_Rec_249055,Human_Splice_Rec_249064,Human_Splice_Rec_249065,Human_Splice_Rec_249073,Human_Splice_Rec_249079,Human_Splice_Rec_249084,Human_Splice_Rec_249090 Human_miRNA_ID_2375855 RMVar_hsa_circ_93810,RMVar_hsa_circ_200115,RMVar_hsa_circ_104113,RMVar_hsa_circ_200116,RMVar_hsa_circ_85349,RMVar_hsa_circ_101559,RMVar_hsa_circ_200124,RMVar_hsa_circ_200125 114351 RMVar_ID_114351 Human_SNP_ID_837691035 m1A Human chr2 - 201729167 201729167 201729167 AATTTTTGCCCTGTAGGCATCTCCAGAATATCAGAAACTGCAGGATTCCAGTTCTTGTTATGAGT AATTTTTGCCCTGTAGGCATCTCCAGAATATCTGAAACTGCAGGATTCCAGTTCTTGTTATGAGT T A ALS2 Ensembl:ENSG00000003393 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:201728554..201729166 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma,lung mixed_adenosquamous_carcinoma 2 lung Human_RBP_ID_25576221 Human_Splice_Rec_346704,Human_Splice_Rec_346750,Human_Splice_Rec_346828,Human_Splice_Rec_346848,Human_Splice_Rec_346858 RMVar_hsa_circ_11516,RMVar_hsa_circ_14968,RMVar_hsa_circ_51022,RMVar_hsa_circ_115319,RMVar_hsa_circ_11844,RMVar_hsa_circ_64444,RMVar_hsa_circ_205931,RMVar_hsa_circ_205930,RMVar_hsa_circ_368566,RMVar_hsa_circ_111652,RMVar_hsa_circ_266997,RMVar_hsa_circ_73934,RMVar_hsa_circ_326745,RMVar_hsa_circ_358297,RMVar_hsa_circ_267811,RMVar_hsa_circ_328835,RMVar_hsa_circ_307610,RMVar_hsa_circ_73155,RMVar_hsa_circ_56926,RMVar_hsa_circ_68755,RMVar_hsa_circ_73501,RMVar_hsa_circ_72321,RMVar_hsa_circ_344808,RMVar_hsa_circ_67007,RMVar_hsa_circ_205936,RMVar_hsa_circ_14650,RMVar_hsa_circ_266604,RMVar_hsa_circ_338194,RMVar_hsa_circ_33427 114352 RMVar_ID_114352 Human_SNP_ID_837703182 m1A Human chr2 - 219615188 219615180 219615188 ACCTTCTCAGAGGCTTCGCCAGATGCTGCTGGAGGAGAGGGCTCTGCCGGGGACCCTGCAGCATC ACCTTCTCAGAGGCTTCGCCAGATGCTGCTGG________GCTCTGCCGGGGACCCTGCAGCATC CCCTCTCCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219615138..219615239 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..40 33 LICA 1 - 114353 RMVar_ID_114353 Human_SNP_ID_837705876 m1A Human chr2 + 120294692 120294692 120294692 CTCCCAAAGAATCATGGGCTTTTTTTTTGAATAAAAAAGCAGACAAATAGACTTTCTCGGGATTT CTCCCAAAGAATCATGGGCTTTTTTTTTGAATTAAAAAGCAGACAAATAGACTTTCTCGGGATTT A T RALB Ensembl:ENSG00000144118 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1137385 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus Human_RBP_ID_533343,Human_RBP_ID_26656792 Human_miRNA_ID_835021 GWAS_ID_8928 RMVar_hsa_circ_82602,RMVar_hsa_circ_202952 114354 RMVar_ID_114354 Human_SNP_ID_837710601 m1A Human chr2 + 64454554 64454554 64454554 TACCCCGCCGCGCCGGGCAAGAAGATGGCGGGATCAGTGGCCGACAGCGATGCCGTGGTGGTGAG TACCCCGCCGCGCCGGGCAAGAAGATGGCGGGGTCAGTGGCCGACAGCGATGCCGTGGTGGTGAG A G LGALSL Ensembl:ENSG00000119862 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:64454429..64454613 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_553552,Human_RBP_ID_4613555 Human_Splice_Rec_253663,Human_Splice_Rec_253669,Human_Splice_Rec_253677,Human_Splice_Rec_253681,Human_Splice_Rec_253689 114355 RMVar_ID_114355 Human_SNP_ID_837721294 m1A Human chr2 - 235788539 235788539 235788539 CTCACCTACCCTCCCGCTCTTCTCCTCGCCCCACCTTGCCTCCCAATCCTCTCCTCACCCCGCCT CTCACCTACCCTCCCGCTCTTCTCCTCGCCCCCCCTTGCCTCCCAATCCTCTCCTCACCCCGCCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235788527..235788624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114356 RMVar_ID_114356 Human_SNP_ID_837791459 m1A Human chr2 + 189001449 189001449 189001449 TCCTCCTGGCCCAGCTGGCCAGCCTGGAGATAAGGTAACCCTTAATACTACCTGGATATAAAAAG TCCTCCTGGCCCAGCTGGCCAGCCTGGAGATAGGGTAACCCTTAATACTACCTGGATATAAAAAG A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:189001376..189001475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung non_small_cell_carcinoma 2 lung Human_Splice_Rec_336328,Human_Splice_Rec_336329,Human_Splice_Rec_336428,Human_Splice_Rec_336429 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_353094,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_27739,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_120084,RMVar_hsa_circ_373125,RMVar_hsa_circ_205231,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_205233 114357 RMVar_ID_114357 Human_SNP_ID_837791460 m1A Human chr2 + 189001449 189001449 189001449 TCCTCCTGGCCCAGCTGGCCAGCCTGGAGATAAGGTAACCCTTAATACTACCTGGATATAAAAAG TCCTCCTGGCCCAGCTGGCCAGCCTGGAGATACGGTAACCCTTAATACTACCTGGATATAAAAAG A C COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:189001376..189001475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 4 haematopoietic and lymphoid tissue Human_Splice_Rec_336328,Human_Splice_Rec_336329,Human_Splice_Rec_336428,Human_Splice_Rec_336429 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_205189,RMVar_hsa_circ_205194,RMVar_hsa_circ_82651,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_78566,RMVar_hsa_circ_14044,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_22017,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217,RMVar_hsa_circ_205219,RMVar_hsa_circ_101254,RMVar_hsa_circ_83531,RMVar_hsa_circ_88349,RMVar_hsa_circ_120630,RMVar_hsa_circ_88735,RMVar_hsa_circ_205220,RMVar_hsa_circ_205222,RMVar_hsa_circ_98065,RMVar_hsa_circ_205221,RMVar_hsa_circ_353573,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_353094,RMVar_hsa_circ_105689,RMVar_hsa_circ_88829,RMVar_hsa_circ_205226,RMVar_hsa_circ_205227,RMVar_hsa_circ_205225,RMVar_hsa_circ_111634,RMVar_hsa_circ_359282,RMVar_hsa_circ_205228,RMVar_hsa_circ_27739,RMVar_hsa_circ_205229,RMVar_hsa_circ_94514,RMVar_hsa_circ_120084,RMVar_hsa_circ_373125,RMVar_hsa_circ_205231,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_205233 114358 RMVar_ID_114358 Human_SNP_ID_837820288 m1A Human chr2 + 175181358 175181358 175181358 ATCCCCCCGACCCTGCCTGGGCTACGCACCAGAGAGGGGGTGCAGGCGAGCTTGGCGCAGGCGAA ATCCCCCCGACCCTGCCTGGGCTACGCACCAGTGAGGGGGTGCAGGCGAGCTTGGCGCAGGCGAA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:175181351..175181475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 114359 RMVar_ID_114359 Human_SNP_ID_837832042 m1A Human chr2 - 159283041 159283041 159283041 GAACATGGTGAAACTGATTCACACATTAGCTGATCATGGTGACGATGTCAACTGCTGTGCCTTCT GAACATGGTGAAACTGATTCACACATTAGCTGTTCATGGTGACGATGTCAACTGCTGTGCCTTCT T A WDSUB1 Ensembl:ENSG00000196151 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:159282990..159283122 26863196 MeRIP-seq:(Medium) rs767210177 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_Splice_Rec_312158,Human_Splice_Rec_312178,Human_Splice_Rec_312190,Human_Splice_Rec_312210,Human_Splice_Rec_312230 Human_miRNA_ID_2721282 RMVar_hsa_circ_306995,RMVar_hsa_circ_350798,RMVar_hsa_circ_204045,RMVar_hsa_circ_14718,RMVar_hsa_circ_302494,RMVar_hsa_circ_275033,RMVar_hsa_circ_204053,RMVar_hsa_circ_204051,RMVar_hsa_circ_204052,RMVar_hsa_circ_288545,RMVar_hsa_circ_316457 114360 RMVar_ID_114360 Human_SNP_ID_837845901 m1A Human chr2 - 73779974 73779974 73779974 TGGCATTGGGTGGGCGGCTTCTTGGGACCCACATGAGCCAGTGGCATCATCCCCGCAGTGGCTGG TGGCATTGGGTGGGCGGCTTCTTGGGACCCACGTGAGCCAGTGGCATCATCCCCGCAGTGGCTGG T C DUSP11 Ensembl:ENSG00000144048 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:73779928..73780060 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_777175,Human_RBP_ID_4623401,Human_RBP_ID_13962455 114361 RMVar_ID_114361 Human_SNP_ID_837847068 m1A Human chr2 + 111495057 111495055 111495057 ATTCCCAATGATGTACACACGACTAAGAAGGAAAAAAAAAAAAGGCGCACACCTCAGCCTTCATT ATTCCCAATGATGTACACACGACTAAGAAGG__AAAAAAAAAAGGCGCACACCTCAGCCTTCATT GAA G AC017002.3,SOCAR Ensembl:ENSG00000280878,Ensembl:ENSG00000240350 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:111495011..111495081 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - 114362 RMVar_ID_114362 Human_SNP_ID_837855069 m1A Human chr2 + 195716852 195716852 195716852 ACCACCACGGCGAGAACAAAACTGTGCTGAGGAAGCATAATCACCAGTGGCACCACAAGCATTCT ACCACCACGGCGAGAACAAAACTGTGCTGAGGTAGCATAATCACCAGTGGCACCACAAGCATTCT A T SLC39A10 Ensembl:ENSG00000196950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:195716801..195716875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_17697946,Human_RBP_ID_26820345 Human_miRNA_ID_2997575 RMVar_hsa_circ_287823,RMVar_hsa_circ_283209,RMVar_hsa_circ_205461,RMVar_hsa_circ_205462,RMVar_hsa_circ_107070,RMVar_hsa_circ_205465,RMVar_hsa_circ_205473,RMVar_hsa_circ_295668,RMVar_hsa_circ_370253,RMVar_hsa_circ_349102,RMVar_hsa_circ_89162,RMVar_hsa_circ_205470,RMVar_hsa_circ_205471,RMVar_hsa_circ_205469,RMVar_hsa_circ_69253,RMVar_hsa_circ_121545,RMVar_hsa_circ_205472,RMVar_hsa_circ_374047,RMVar_hsa_circ_205474,RMVar_hsa_circ_300686,RMVar_hsa_circ_317483,RMVar_hsa_circ_374249,RMVar_hsa_circ_205475 114363 RMVar_ID_114363 Human_SNP_ID_837863736 m1A Human chr2 + 33584953 33584953 33584953 CCTCGGCCTCCACGACCACCTCGCCCACCACGACCACCACCACGATCACCATGGTGCCCGCCATC CCTCGGCCTCCACGACCACCTCGCCCACCACGGCCACCACCACGATCACCATGGTGCCCGCCATC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:33584908..33585046 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 114364 RMVar_ID_114364 Human_SNP_ID_837888013 m1A Human chr2 + 113157506 113157485 113157506 GCGCGGGGCCGTGGGGCGCGCGGGCCCGCGGGAGGCCGGAGCAGGAGCCCGGCGGGAAATGGGTA GCGCGGGGCCGT_____________________GGCCGGAGCAGGAGCCCGGCGGGAAATGGGTA TGGGGCGCGCGGGCCCGCGGGA T PSD4 Ensembl:ENSG00000125637 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:113157460..113157525 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 13..33 33 PRAD 1 - Human_RBP_ID_18422316 Human_Splice_Rec_289681 114365 RMVar_ID_114365 Human_SNP_ID_837899995 m1A Human chr2 - 223877328 223877328 223877328 ATAGCAACAGTATCTTTGCTAATCTTACTAATAGATATTGATTAAAAAAAAAAAACCTCAGTACT ATAGCAACAGTATCTTTGCTAATCTTACTAATGGATATTGATTAAAAAAAAAAAACCTCAGTACT T C WDFY1,AC093884.1 Ensembl:ENSG00000085449,Ensembl:ENSG00000286239 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9795 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_26488235 GWAS_ID_10116,GWAS_ID_10117,GWAS_ID_10118,GWAS_ID_10119,GWAS_ID_10120,GWAS_ID_10121,GWAS_ID_10122,GWAS_ID_10123,GWAS_ID_10124,GWAS_ID_10125,GWAS_ID_10126,GWAS_ID_10127,GWAS_ID_10128,GWAS_ID_10129,GWAS_ID_10130,GWAS_ID_10131,GWAS_ID_10132,GWAS_ID_10133,GWAS_ID_10134,GWAS_ID_10135,GWAS_ID_10136,GWAS_ID_10137,GWAS_ID_10138,GWAS_ID_10139,GWAS_ID_10140,GWAS_ID_10141,GWAS_ID_10142,GWAS_ID_10143,GWAS_ID_10144,GWAS_ID_10145,GWAS_ID_10146,GWAS_ID_10147,GWAS_ID_10148,GWAS_ID_10149,GWAS_ID_10150 RMVar_hsa_circ_100226,RMVar_hsa_circ_207233 114366 RMVar_ID_114366 Human_SNP_ID_837909909 m1A Human chr2 - 74527227 74527227 74527227 TCTGCCTCCAAGGTGAGACCCAGGAAATGGTCAGATCCAAGTGTTGGGGTGAGTTGGGGGCAGGC TCTGCCTCCAAGGTGAGACCCAGGAAATGGTCGGATCCAAGTGTTGGGGTGAGTTGGGGGCAGGC T C AUP1 Ensembl:ENSG00000115307 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74527224..74527363 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_19100768 RMVar_hsa_circ_98500,RMVar_hsa_circ_123063,RMVar_hsa_circ_125197,RMVar_hsa_circ_115371,RMVar_hsa_circ_201374,RMVar_hsa_circ_201376,RMVar_hsa_circ_201377,RMVar_hsa_circ_201375 114367 RMVar_ID_114367 Human_SNP_ID_837962786 m1A Human chr2 + 27375677 27375677 27375677 GCCAGCAACTCCGAGAAGGCTCCTTCCGGGTCACCCGCATGCGATGCTGGCGGGTCACCTCCTCT GCCAGCAACTCCGAGAAGGCTCCTTCCGGGTCGCCCGCATGCGATGCTGGCGGGTCACCTCCTCT A G SNX17 Ensembl:ENSG00000115234 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:27375626..27375725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_Splice_Rec_228611,Human_Splice_Rec_228641,Human_Splice_Rec_228667,Human_Splice_Rec_228711,Human_Splice_Rec_228743 Human_miRNA_ID_2440320 RMVar_hsa_circ_87588,RMVar_hsa_circ_197995,RMVar_hsa_circ_97893,RMVar_hsa_circ_117732,RMVar_hsa_circ_197997,RMVar_hsa_circ_114816,RMVar_hsa_circ_197998,RMVar_hsa_circ_79525,RMVar_hsa_circ_197999,RMVar_hsa_circ_119307,RMVar_hsa_circ_111791,RMVar_hsa_circ_198000,RMVar_hsa_circ_198001,RMVar_hsa_circ_90954,RMVar_hsa_circ_198002,RMVar_hsa_circ_198003 114368 RMVar_ID_114368 Human_SNP_ID_837966404 m1A Human chr2 + 158680535 158680535 158680535 TCCTCATAGCTATGAAGATCCTTATTTTGATGACCGAGTTCACTTTCCAGCTTCTACTGATTACT TCCTCATAGCTATGAAGATCCTTATTTTGATGTCCGAGTTCACTTTCCAGCTTCTACTGATTACT A T PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158680485..158680635 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_RBP_ID_536353,Human_RBP_ID_2597455,Human_RBP_ID_17277966 Human_miRNA_ID_173121 RMVar_hsa_circ_204008,RMVar_hsa_circ_88828,RMVar_hsa_circ_79124,RMVar_hsa_circ_204011 114369 RMVar_ID_114369 Human_SNP_ID_837972876 m1A Human chr2 - 63622594 63622594 63622594 TATTTCCTGCCAATGTTGCTCACTCGGTGTACATCCTGGAGGACTCTATTGTGGACCCACAGAAT TATTTCCTGCCAATGTTGCTCACTCGGTGTACGTCCTGGAGGACTCTATTGTGGACCCACAGAAT T C WDPCP,AC016734.1 Ensembl:ENSG00000143951,Ensembl:ENSG00000228305 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs900136906 Functional Loss SNV ICGC 33..33 33 LAML 2 - 114370 RMVar_ID_114370 Human_SNP_ID_837975885 m1A Human chr2 + 36522082 36522082 36522082 CAACAGCATCTTCTTTGCTGACCTATATGTTCATTTTTCCAGATCAACCTTTTCGGCCTTCCTTG CAACAGCATCTTCTTTGCTGACCTATATGTTCGTTTTTCCAGATCAACCTTTTCGGCCTTCCTTG A G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:36522076..36522125 32194978 MeRIP-seq:(Medium) rs767770023 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_88426,RMVar_hsa_circ_89605,RMVar_hsa_circ_198723,RMVar_hsa_circ_79194,RMVar_hsa_circ_198724,RMVar_hsa_circ_198722,RMVar_hsa_circ_198766,RMVar_hsa_circ_77243,RMVar_hsa_circ_323591,RMVar_hsa_circ_372785,RMVar_hsa_circ_275079,RMVar_hsa_circ_80290,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738,RMVar_hsa_circ_291872,RMVar_hsa_circ_373984,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_126754,RMVar_hsa_circ_198755,RMVar_hsa_circ_198753,RMVar_hsa_circ_198754,RMVar_hsa_circ_198752,RMVar_hsa_circ_119470,RMVar_hsa_circ_124582,RMVar_hsa_circ_114286,RMVar_hsa_circ_198768,RMVar_hsa_circ_198767,RMVar_hsa_circ_12447,RMVar_hsa_circ_198776,RMVar_hsa_circ_283755,RMVar_hsa_circ_198765,RMVar_hsa_circ_332230,RMVar_hsa_circ_104139,RMVar_hsa_circ_96900,RMVar_hsa_circ_198774,RMVar_hsa_circ_198775,RMVar_hsa_circ_371470,RMVar_hsa_circ_277596,RMVar_hsa_circ_313176,RMVar_hsa_circ_198784,RMVar_hsa_circ_198786,RMVar_hsa_circ_198787,RMVar_hsa_circ_198785,RMVar_hsa_circ_370520,RMVar_hsa_circ_97131,RMVar_hsa_circ_198799,RMVar_hsa_circ_198796,RMVar_hsa_circ_198797,RMVar_hsa_circ_326951,RMVar_hsa_circ_282278,RMVar_hsa_circ_82537,RMVar_hsa_circ_198800,RMVar_hsa_circ_127007,RMVar_hsa_circ_371567,RMVar_hsa_circ_198798,RMVar_hsa_circ_270432,RMVar_hsa_circ_75690,RMVar_hsa_circ_198807,RMVar_hsa_circ_198808,RMVar_hsa_circ_198809,RMVar_hsa_circ_198806,RMVar_hsa_circ_118006,RMVar_hsa_circ_283672,RMVar_hsa_circ_78790,RMVar_hsa_circ_198811,RMVar_hsa_circ_198812,RMVar_hsa_circ_198810,RMVar_hsa_circ_375626,RMVar_hsa_circ_198817,RMVar_hsa_circ_325688,RMVar_hsa_circ_198815,RMVar_hsa_circ_370808,RMVar_hsa_circ_83089,RMVar_hsa_circ_98512,RMVar_hsa_circ_198819,RMVar_hsa_circ_198820,RMVar_hsa_circ_198818 114371 RMVar_ID_114371 Human_SNP_ID_837980918 m1A Human chr2 - 241682911 241682911 241682911 TATTTCTTTTTTGTTTTCCTCGAGACAGTTTCATTCTTGTCGCCCAGACTGGAGTGCAATGGGGC TATTTCTTTTTTGTTTTCCTCGAGACAGTTTCGTTCTTGTCGCCCAGACTGGAGTGCAATGGGGC T C DTYMK Ensembl:ENSG00000168393 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4347866 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_13827336 Human_Splice_Rec_383280 114372 RMVar_ID_114372 Human_SNP_ID_838003887 m1A Human chr2 - 234495947 234495947 234495947 AGTGCGTCAAGAAAGAATGAATGGATGGATGGATGGTTGGATGGATGGATGGATGGATGAGCGAG AGTGCGTCAAGAAAGAATGAATGGATGGATGGTTGGTTGGATGGATGGATGGATGGATGAGCGAG T A ARL4C Ensembl:ENSG00000188042 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:234495899..234495992 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_RBP_ID_546148,Human_RBP_ID_23858010 Human_miRNA_ID_3062324 RMVar_hsa_circ_207753,RMVar_hsa_circ_114711 114373 RMVar_ID_114373 Human_SNP_ID_838005150 m1A Human chr2 + 203441282 203441282 203441282 GGAGGAGGGGGTGGTGGAGGGGGTGGTGGAGGAGGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG GGAGGAGGGGGTGGTGGAGGGGGTGGTGGAGGGGGAGGTGGGGGTGGCGGAGGAGGTAGAGGTGG A G ABI2 Ensembl:ENSG00000138443 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:203441233..203441384 26863196 MeRIP-seq:(Medium) rs777698648 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 5 lung Human_RBP_ID_8200773 114374 RMVar_ID_114374 Human_SNP_ID_838005196 m1A Human chr2 - 219557883 219557883 219557883 AGGCTGCAGGCCCAGCCCATGCAGGGCTCTACACCTGCCAGTCTGGAGCAGCCCCCGGAGCCCCA AGGCTGCAGGCCCAGCCCATGCAGGGCTCTACCCCTGCCAGTCTGGAGCAGCCCCCGGAGCCCCA T G OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219557832..219558205 32194978 MeRIP-seq:(Medium) rs745987417 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,THCA,head_neck squamous_cell_carcinoma 56 head and neck Human_Splice_Rec_364023,Human_Splice_Rec_364071,Human_Splice_Rec_364103,Human_Splice_Rec_364141,Human_Splice_Rec_364151,Human_Splice_Rec_364159 RMVar_hsa_circ_69046 114375 RMVar_ID_114375 Human_SNP_ID_838009820 m1A Human chr2 - 225513501 225513501 225513501 GTCTGTGCCCCCAACCGAGTGCAGGGACTGTGATCTCACAGAAAAGCCACTGGAGCAAGGATGGG GTCTGTGCCCCCAACCGAGTGCAGGGACTGTGGTCTCACAGAAAAGCCACTGGAGCAAGGATGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:225513451..225513675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114376 RMVar_ID_114376 Human_SNP_ID_838012189 m1A Human chr2 - 174248503 174248503 174248503 CTCCTTCCTCCCCGCCTCCAGCTGCCGGCAGGACCTTTCTCTCGCTGCCGCTGGGACCCCGTGTC CTCCTTCCTCCCCGCCTCCAGCTGCCGGCAGGCCCTTTCTCTCGCTGCCGCTGGGACCCCGTGTC T G OLA1 Ensembl:ENSG00000138430 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:174248407..174248550;chr2:174248402..174248557;chr2:174248392..174248550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_243345,Human_RBP_ID_4587204,Human_RBP_ID_17944336 Human_Splice_Rec_325185,Human_Splice_Rec_325205,Human_Splice_Rec_325223 114377 RMVar_ID_114377 Human_SNP_ID_838036037 m1A Human chr2 + 172088530 172088530 172088530 TGCCACCTGAGACAGCCCAAGCAGCAAGATAAACCCGCTCCACCCGACCCGCCGACCTTCAGCTT TGCCACCTGAGACAGCCCAAGCAGCAAGATAACCCCGCTCCACCCGACCCGCCGACCTTCAGCTT A C DLX1 Ensembl:ENSG00000144355 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:172088481..172088622 26863196 MeRIP-seq:(Medium) rs1023380288 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114378 RMVar_ID_114378 Human_SNP_ID_838041244 m1A Human chr2 + 74557175 74557175 74557175 GGGGACCATGGGGAGGTGGCACTAGGGATCAAAGAAGATGGTTAGAACCAGCAGAAGCCAGAGGG GGGGACCATGGGGAGGTGGCACTAGGGATCAACGAAGATGGTTAGAACCAGCAGAAGCCAGAGGG A C DOK1 Ensembl:ENSG00000115325 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:74557125..74557306 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_5146840 114379 RMVar_ID_114379 Human_SNP_ID_838046944 m1A Human chr2 - 1655961 1655961 1655961 TATGTTTGATGGGCTATGTGCGTGTTATTTATAAGGTGCTGGGTGTGTTGTATTTGTGTGGTGTG TATGTTTGATGGGCTATGTGCGTGTTATTTATCAGGTGCTGGGTGTGTTGTATTTGTGTGGTGTG T G PXDN Ensembl:ENSG00000130508 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:1655951..1656208 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_23834431 RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626 114380 RMVar_ID_114380 Human_SNP_ID_838057019 m1A Human chr2 + 167293177 167293177 167293177 TCTTGCAGGCGGCCGCCGGGGAGGGGCGGCCGAGAGAGCGGAGCACGAGGAGGCGGGGGCGGCAG TCTTGCAGGCGGCCGCCGGGGAGGGGCGGCCGGGAGAGCGGAGCACGAGGAGGCGGGGGCGGCAG A G AC073050.1 Ensembl:ENSG00000228222 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:167293126..167293197 26863196 MeRIP-seq:(Medium) rs868133496 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114381 RMVar_ID_114381 Human_SNP_ID_838066087 m1A Human chr2 - 177219316 177219316 177219316 TTTATCATCATAATAAAAATTTAAAGATACCTACCCTTTTCTGCTGTTTTTAGAACCTTCTGCTA TTTATCATCATAATAAAAATTTAAAGATACCTCCCCTTTTCTGCTGTTTTTAGAACCTTCTGCTA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA heat shock 4h chr2:177219182..177219401;chr2:177219276..177219325 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 114382 RMVar_ID_114382 Human_SNP_ID_838078527 m1A Human chr2 + 32618228 32618225 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTATT___TTTTTTTTTTACTATAGAGTGAGGGGTTGTTA TTTA T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 31..33 33 UCEC 10 - Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 114383 RMVar_ID_114383 Human_SNP_ID_838080954 m1A Human chr2 - 229180829 229180829 229180829 CGAAGGGACAGGCAATGGCCTCCCTTGCCCTCAGCGGATCGAAAGGGAGTCGGGTTCAGATCCCC CGAAGGGACAGGCAATGGCCTCCCTTGCCCTCGGCGGATCGAAAGGGAGTCGGGTTCAGATCCCC T C PID1 Ensembl:ENSG00000153823 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:229180731..229181090;chr2:229180738..229181097;chr2:229180738..229180899 26863196 MeRIP-seq:(Medium) rs78860008 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,frontal_lobe astrocytoma_Grade_III,LMS,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_II,frontal_lobe oligodendroglioma_Grade_III 14 brain Human_RBP_ID_270321,Human_RBP_ID_280687,Human_RBP_ID_1098468,Human_RBP_ID_1197384,Human_RBP_ID_1584090,Human_RBP_ID_2625438,Human_RBP_ID_4598728,Human_RBP_ID_5199903,Human_RBP_ID_5275690,Human_RBP_ID_5422822,Human_RBP_ID_5589059,Human_RBP_ID_6972677,Human_RBP_ID_8513414,Human_RBP_ID_8846057,Human_RBP_ID_9103674,Human_RBP_ID_13789207,Human_RBP_ID_17015051,Human_RBP_ID_17063690,Human_RBP_ID_17068869,Human_RBP_ID_17135121,Human_RBP_ID_17192636,Human_RBP_ID_17698608,Human_RBP_ID_17966823,Human_RBP_ID_18180338,Human_RBP_ID_18200861,Human_RBP_ID_18208876,Human_RBP_ID_18755489,Human_RBP_ID_20437284,Human_RBP_ID_22422690,Human_RBP_ID_22990011,Human_RBP_ID_23182310,Human_RBP_ID_23310660,Human_RBP_ID_23855889,Human_RBP_ID_26488240,Human_RBP_ID_26663912,Human_RBP_ID_26749885,Human_RBP_ID_27007556,Human_RBP_ID_27158802,Human_RBP_ID_27287271 RMVar_hsa_circ_354719,RMVar_hsa_circ_361298,RMVar_hsa_circ_207384 114384 RMVar_ID_114384 Human_SNP_ID_838099606 m1A Human chr2 + 54456503 54456503 54456503 GAGCGGGAGGAGGACGGGACCCCGGCGCCCCCACCCCATCCCCGGGAGGTAGGTAGGGGGCCCGA GAGCGGGAGGAGGACGGGACCCCGGCGCCCCCCCCCCATCCCCGGGAGGTAGGTAGGGGGCCCGA A C SPTBN1 Ensembl:ENSG00000115306 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:54456301..54456601 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_4622403 Human_Splice_Rec_245743,Human_Splice_Rec_245817 114385 RMVar_ID_114385 Human_SNP_ID_838117642 m1A Human chr2 + 120261835 120261835 120261835 GAGGCCAATGCTTGCAGGTGTCAAGAGGGCAGAGAATTGTGTGTGGGGGTGGTATTTGAACAAGT GAGGCCAATGCTTGCAGGTGTCAAGAGGGCAGTGAATTGTGTGTGGGGGTGGTATTTGAACAAGT A T RALB Ensembl:ENSG00000144118 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:120261832..120262083 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114386 RMVar_ID_114386 Human_SNP_ID_838122603 m1A Human chr2 - 47403247 47403247 47403247 GCTTCTCCGGCATGCCCTGAAAGAAGCGCACGAAGCCGACCTCGGCCGCGCTCTCCAACTGCAGC GCTTCTCCGGCATGCCCTGAAAGAAGCGCACGGAGCCGACCTCGGCCGCGCTCTCCAACTGCAGC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T cell line,total RNA;HEK293T,ALKBH3 KO chr2:47403147..47403297;chr2:47403159..47403252 26863196,26863410 MeRIP-seq:(Medium) rs1320061495 Functional Loss SNV COSMIC 33..33 33 cervix small_cell_carcinoma 4 uterus 114387 RMVar_ID_114387 Human_SNP_ID_838145610 m1A Human chr2 + 230877541 230877541 230877541 GGAAAGACACCTACCGGCTCCGGCGCCGGGCAACGCGGAGGCGTGAGTGGCTGGCTTCACCCACA GGAAAGACACCTACCGGCTCCGGCGCCGGGCAGCGCGGAGGCGTGAGTGGCTGGCTTCACCCACA A G ITM2C Ensembl:ENSG00000135916 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:230877449..230877575 26863196 MeRIP-seq:(Medium) rs748984665 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_22766302 Human_Splice_Rec_369149,Human_Splice_Rec_369157,Human_Splice_Rec_369165,Human_Splice_Rec_369181 114388 RMVar_ID_114388 Human_SNP_ID_838147331 m1A Human chr2 - 38751321 38751321 38751321 GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT GCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCCGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCT T G SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:38751060..38751375 26863196 MeRIP-seq:(Medium) rs570745972 Functional Loss SNV COSMIC 33..33 33 breast HER-positive_carcinoma 3 breast Human_RBP_ID_58102,Human_RBP_ID_1196050,Human_RBP_ID_1586765,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 114389 RMVar_ID_114389 Human_SNP_ID_838170184 m1A Human chr2 - 232458700 232458700 232458700 CACGTCTGGTCGCACGCCTGAGTTGAACACGTAGCCCGGGCCATTGCCGTACAGGATGGACGTGT CACGTCTGGTCGCACGCCTGAGTTGAACACGTGGCCCGGGCCATTGCCGTACAGGATGGACGTGT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:232458426..232458746 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114390 RMVar_ID_114390 Human_SNP_ID_838172821 m1A Human chr2 - 55235508 55235508 55235508 CAACATTTGCCACAATAATGTCTGTCAAAGTGACTTGCCATAAACACCCCAGCACCACATTCATC CAACATTTGCCACAATAATGTCTGTCAAAGTGGCTTGCCATAAACACCCCAGCACCACATTCATC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55235399..55235546 26863196 MeRIP-seq:(Medium) rs973413098 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 114391 RMVar_ID_114391 Human_SNP_ID_838180575 m1A Human chr2 - 74211868 74211868 74211868 ATTTCATTTTTAAAAATAAAATTTCACCATTTACCTTCAAAATCCACATCTCCAACCAACTTGGG ATTTCATTTTTAAAAATAAAATTTCACCATTTGCCTTCAAAATCCACATCTCCAACCAACTTGGG T C AC006030.1 Ensembl:ENSG00000264324 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:74211824..74214534 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114392 RMVar_ID_114392 Human_SNP_ID_838203645 m1A Human chr2 + 210606912 210606906 210606913 TGCATCATTGAAGTGAATGCCAGACTGTCCCGAAGCTCTGCTCTGGCCTCAAAAGCCACTGGGTA TGCATCATTGAAGTGAATGCCAGACTG_______GCTCTGCTCTGGCCTCAAAAGCCACTGGGTA GTCCCGAA G CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210606697..210606981 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 28..34 33 UCEC 1 - Human_Splice_Rec_353117,Human_Splice_Rec_353195,Human_Splice_Rec_353271,Human_Splice_Rec_353347,Human_Splice_Rec_353421,Human_Splice_Rec_353503,Human_Splice_Rec_353557,Human_Splice_Rec_353605 Human_miRNA_ID_2251102 RMVar_hsa_circ_17150,RMVar_hsa_circ_297846,RMVar_hsa_circ_355019,RMVar_hsa_circ_366902,RMVar_hsa_circ_309769,RMVar_hsa_circ_312562,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_72954,RMVar_hsa_circ_8923,RMVar_hsa_circ_367528,RMVar_hsa_circ_69514,RMVar_hsa_circ_100412,RMVar_hsa_circ_70074,RMVar_hsa_circ_55652,RMVar_hsa_circ_206567,RMVar_hsa_circ_352345,RMVar_hsa_circ_360389,RMVar_hsa_circ_80365,RMVar_hsa_circ_70790,RMVar_hsa_circ_206569,RMVar_hsa_circ_29829,RMVar_hsa_circ_73146,RMVar_hsa_circ_24212,RMVar_hsa_circ_58944,RMVar_hsa_circ_86182,RMVar_hsa_circ_58863,RMVar_hsa_circ_206571,RMVar_hsa_circ_107306,RMVar_hsa_circ_81683,RMVar_hsa_circ_206572,RMVar_hsa_circ_58434,RMVar_hsa_circ_206573 114393 RMVar_ID_114393 Human_SNP_ID_838213010 m1A Human chr2 - 11402350 11402350 11402350 CTTCTTCTCTCCTCCCTCTTGACTCTTTTCCCACCCGCCTCCTGCCATTGACTCCAGCCTATAGA CTTCTTCTCTCCTCCCTCTTGACTCTTTTCCCCCCCGCCTCCTGCCATTGACTCCAGCCTATAGA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:11402302..11402464 26863196 MeRIP-seq:(Medium) rs1015616216 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 114394 RMVar_ID_114394 Human_SNP_ID_838218453 m1A Human chr2 + 104856451 104856451 104856451 TGGACTCAACAGCCACGACCCGCACTCGGACGAGGACACGCCGACGTCGGACGACCTGGAGCAGT TGGACTCAACAGCCACGACCCGCACTCGGACGGGGACACGCCGACGTCGGACGACCTGGAGCAGT A G AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:104856152..104856499 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1135565 114395 RMVar_ID_114395 Human_SNP_ID_838218454 m1A Human chr2 + 104856451 104856451 104856451 TGGACTCAACAGCCACGACCCGCACTCGGACGAGGACACGCCGACGTCGGACGACCTGGAGCAGT TGGACTCAACAGCCACGACCCGCACTCGGACGTGGACACGCCGACGTCGGACGACCTGGAGCAGT A T AC018730.1,POU3F3 Ensembl:ENSG00000269707,Ensembl:ENSG00000198914 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:104856152..104856499 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_1135565 114396 RMVar_ID_114396 Human_SNP_ID_838269355 m1A Human chr2 - 27343554 27343554 27343554 GTATGCAGGGGCAGCCATTTTGGGGGGTGCTGATGGATACCTGCGGGGTCGGCTATGTTGCCCTG GTATGCAGGGGCAGCCATTTTGGGGGGTGCTGGTGGATACCTGCGGGGTCGGCTATGTTGCCCTG T C GTF3C2 Ensembl:ENSG00000115207 Protein coding start codon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:27343443..27343600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_4605705,Human_RBP_ID_5089056,Human_RBP_ID_5528418,Human_RBP_ID_9330395,Human_RBP_ID_17954884,Human_RBP_ID_18193270,Human_RBP_ID_22077514,Human_RBP_ID_22250444,Human_RBP_ID_22451192,Human_RBP_ID_22548166,Human_RBP_ID_23119403 Human_Splice_Rec_228168,Human_Splice_Rec_228204,Human_Splice_Rec_228318,Human_Splice_Rec_228324 Human_miRNA_ID_3062163 RMVar_hsa_circ_4065,RMVar_hsa_circ_110068,RMVar_hsa_circ_197975,RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_21353,RMVar_hsa_circ_25458,RMVar_hsa_circ_197985,RMVar_hsa_circ_15678,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_339766,RMVar_hsa_circ_368158,RMVar_hsa_circ_197987 114397 RMVar_ID_114397 Human_SNP_ID_838279133 m1A Human chr2 + 152656246 152656242 152656246 TAAAACCCAGTGTTATTTCAGTTGAACTTAAAATAGAGTCCCTGGTCTGAATCAGACTTTAAATC TAAAACCCAGTGTTATTTCAGTTGAACTT____TAGAGTCCCTGGTCTGAATCAGACTTTAAATC TAAAA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:152655935..152656286 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 PRAD 1 - 114398 RMVar_ID_114398 Human_SNP_ID_838296118 m1A Human chr2 - 74198730 74198730 74198730 GAGCTCTGTGACCCTCTTACCGAACTGCCGCGAGGTGGAAAGGGCGAAGGCGAAGGGAGCAGCTG GAGCTCTGTGACCCTCTTACCGAACTGCCGCGTGGTGGAAAGGGCGAAGGCGAAGGGAGCAGCTG T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:74198612..74198750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114399 RMVar_ID_114399 Human_SNP_ID_838348139 m1A Human chr2 - 232458754 232458754 232458754 CCCTGGTCCCCCTGCACGGGCCATTCAGCCTCACTCACCGCTCTCGCTCTCATTCACGTCTGGTC CCCTGGTCCCCCTGCACGGGCCATTCAGCCTCGCTCACCGCTCTCGCTCTCATTCACGTCTGGTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr2:232458751..232458775;chr2:232458751..232458800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114400 RMVar_ID_114400 Human_SNP_ID_838353782 m1A Human chr2 - 231458385 231458385 231458385 AGAGCTCATTTTTGTTTTTTTAATCTAGAGCGAGATGCGAGAACACTTTTGGCTAAAAATCTCCC AGAGCTCATTTTTGTTTTTTTAATCTAGAGCGCGATGCGAGAACACTTTTGGCTAAAAATCTCCC T G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_922602,Human_RBP_ID_1022264,Human_RBP_ID_1584206,Human_RBP_ID_1912528,Human_RBP_ID_6895070,Human_RBP_ID_8846333,Human_RBP_ID_13794673,Human_RBP_ID_17506467,Human_RBP_ID_22670482,Human_RBP_ID_22990245,Human_RBP_ID_23856647,Human_RBP_ID_25520329,Human_RBP_ID_26340360 Human_Splice_Rec_369914,Human_Splice_Rec_369974 Human_miRNA_ID_2667633 RMVar_hsa_circ_69694,RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207590,RMVar_hsa_circ_75733,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_62733,RMVar_hsa_circ_348562 114401 RMVar_ID_114401 Human_SNP_ID_838378547 m1A Human chr2 - 202376572 202376572 202376572 CTCCCGTCAATGGCTCCTGTGAGCGAATCACAACCCCCCGAGGAAGCCGCTGCTGCTGCCGCCGC CTCCCGTCAATGGCTCCTGTGAGCGAATCACACCCCCCCGAGGAAGCCGCTGCTGCTGCCGCCGC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:202376376..202376673 26863196 MeRIP-seq:(Medium) rs935220982 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114402 RMVar_ID_114402 Human_SNP_ID_838397500 m1A Human chr2 + 85596614 85596600 85596615 GCCTCCACCAGCTGCCAAGACTGTGGTTGAGAACCTCCCCAGGACAGTCATCAGAGGCTCTCAGG GCCTCCACCAGCTGCCAAG_______________CTCCCCAGGACAGTCATCAGAGGCTCTCAGG GACTGTGGTTGAGAAC G RNF181 Ensembl:ENSG00000168894 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:85596501..85596625 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 20..34 33 BLCA 1 - Human_RBP_ID_776448,Human_RBP_ID_1924118,Human_RBP_ID_4618407,Human_RBP_ID_9112806,Human_RBP_ID_22450446,Human_RBP_ID_26818690 Human_Splice_Rec_268936,Human_Splice_Rec_268938,Human_Splice_Rec_268939,Human_Splice_Rec_268944,Human_Splice_Rec_268945,Human_Splice_Rec_268952,Human_Splice_Rec_268953,Human_Splice_Rec_268956,Human_Splice_Rec_268957,Human_Splice_Rec_268964,Human_Splice_Rec_268965 Human_miRNA_ID_843369,Human_miRNA_ID_2038639,Human_miRNA_ID_2365988,Human_miRNA_ID_3013791,Human_miRNA_ID_3017621 RMVar_hsa_circ_8601,RMVar_hsa_circ_127154,RMVar_hsa_circ_44140,RMVar_hsa_circ_201570 114403 RMVar_ID_114403 Human_SNP_ID_838401582 m1A Human chr2 - 86720719 86720719 86720719 GCCGCGCTCGCACAGCTGCCCGTAGCCTGAGAACTTGTGCAGCACCTTCTCCAGCTCGCGCTCCA GCCGCGCTCGCACAGCTGCCCGTAGCCTGAGAGCTTGTGCAGCACCTTCTCCAGCTCGCGCTCCA T C RNF103-CHMP3 Ensembl:ENSG00000249884 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:86720619..86720719 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114404 RMVar_ID_114404 Human_SNP_ID_838414963 m1A Human chr2 + 210668275 210668275 210668275 GGATTTAAGATACCCCAGAAAGGCATCCTGATAGGCATCCAGGTAAGTGGTTTGTGGCTGTGTGC GGATTTAAGATACCCCAGAAAGGCATCCTGATTGGCATCCAGGTAAGTGGTTTGTGGCTGTGTGC A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210668134..210668337 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_304509,Human_RBP_ID_24378714 Human_Splice_Rec_353148,Human_Splice_Rec_353149,Human_Splice_Rec_353226,Human_Splice_Rec_353227,Human_Splice_Rec_353302,Human_Splice_Rec_353303,Human_Splice_Rec_353378,Human_Splice_Rec_353379,Human_Splice_Rec_353452,Human_Splice_Rec_353453,Human_Splice_Rec_353534,Human_Splice_Rec_353535,Human_Splice_Rec_353588,Human_Splice_Rec_353589,Human_Splice_Rec_353638,Human_Splice_Rec_353639,Human_Splice_Rec_353668,Human_Splice_Rec_353669,Human_Splice_Rec_353682,Human_Splice_Rec_353683 RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_6014,RMVar_hsa_circ_56320,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_103202,RMVar_hsa_circ_368273,RMVar_hsa_circ_353791,RMVar_hsa_circ_56784,RMVar_hsa_circ_206577,RMVar_hsa_circ_6227,RMVar_hsa_circ_360599,RMVar_hsa_circ_71865,RMVar_hsa_circ_70591,RMVar_hsa_circ_113456,RMVar_hsa_circ_206578 114405 RMVar_ID_114405 Human_SNP_ID_838441827 m1A Human chr2 - 238444635 238444635 238444635 CTGGGCCCAGCGATTCCCACTTCACTAGATTCAGGTTGGCTCCAAATTCTACCAGCAGGCTCACG CTGGGCCCAGCGATTCCCACTTCACTAGATTCGGGTTGGCTCCAAATTCTACCAGCAGGCTCACG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:238435726..238444650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 114406 RMVar_ID_114406 Human_SNP_ID_838447728 m1A Human chr2 + 219559314 219559314 219559314 CCCCGTCCTCGGGCTGAGCAGCAGGTAGCACCAGGCGGCAGCGTGGCCCATCCCTCTCCAGCACC CCCCGTCCTCGGGCTGAGCAGCAGGTAGCACCGGGCGGCAGCGTGGCCCATCCCTCTCCAGCACC A G AC009955.4 Ensembl:ENSG00000269068 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:219559268..219559478 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 114407 RMVar_ID_114407 Human_SNP_ID_838450997 m1A Human chr2 - 241256297 241256297 241256297 GACTGGTTGGCGAGATCATGCAGGAGACAGGCACGCGCATCAACATCCCCCCACCCAGCGTGAAC GACTGGTTGGCGAGATCATGCAGGAGACAGGCGCGCGCATCAACATCCCCCCACCCAGCGTGAAC T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241256176..241256345 26863196 MeRIP-seq:(Medium) rs1380894489 Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_5196345,Human_RBP_ID_5589219,Human_RBP_ID_9259973,Human_RBP_ID_18193441,Human_RBP_ID_26340536 Human_miRNA_ID_2224906,Human_miRNA_ID_2652956,Human_miRNA_ID_2754152 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_78553,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_63419,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_375899,RMVar_hsa_circ_279198,RMVar_hsa_circ_371246,RMVar_hsa_circ_208089,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_302446,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_208092,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_20829 114408 RMVar_ID_114408 Human_SNP_ID_838473960 m1A Human chr2 + 60756347 60756347 60756347 GTGTTTTCACTACTCGGTTGGATGCCTCAGCCATAGTAAGTGGGAAAGTGAGCGAGCAAGCGAGC GTGTTTTCACTACTCGGTTGGATGCCTCAGCCGTAGTAAGTGGGAAAGTGAGCGAGCAAGCGAGC A G PAPOLG Ensembl:ENSG00000115421 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:60756296..60756431 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_4623327,Human_RBP_ID_18421780,Human_RBP_ID_26340930 Human_Splice_Rec_250189,Human_Splice_Rec_250225 RMVar_hsa_circ_113762,RMVar_hsa_circ_200182 114409 RMVar_ID_114409 Human_SNP_ID_838494377 m1A Human chr2 - 70258210 70258210 70258210 CTCGGGGCATCCGCAGCTGCACAGCAACAGCCACAACCCCAGCAGCGAGGAGACGAGCTCCGCGA CTCGGGGCATCCGCAGCTGCACAGCAACAGCCGCAACCCCAGCAGCGAGGAGACGAGCTCCGCGA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:70258160..70258419 26863196 MeRIP-seq:(Medium) rs760785610 Functional Loss SNV ICGC 33..33 33 NACA 1 - 114410 RMVar_ID_114410 Human_SNP_ID_838508482 m1A Human chr2 - 231460752 231460752 231460752 GGCTGAGGATGAAGATGAAGAAGAGGATGATGAGGACGAGGATGACGACGACGACGAAGATGATG GGCTGAGGATGAAGATGAAGAAGAGGATGATGGGGACGAGGATGACGACGACGACGAAGATGATG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:231460551..231460875 26863196 MeRIP-seq:(Medium) rs758559474 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_545751,Human_RBP_ID_774983,Human_RBP_ID_829701,Human_RBP_ID_920616,Human_RBP_ID_1299877,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627049,Human_RBP_ID_3618016,Human_RBP_ID_4599478,Human_RBP_ID_5194520,Human_RBP_ID_5501793,Human_RBP_ID_5589079,Human_RBP_ID_6895102,Human_RBP_ID_8257488,Human_RBP_ID_8513813,Human_RBP_ID_8846342,Human_RBP_ID_9385635,Human_RBP_ID_9975863,Human_RBP_ID_13794780,Human_RBP_ID_17275388,Human_RBP_ID_17390555,Human_RBP_ID_17506476,Human_RBP_ID_18443191,Human_RBP_ID_18533503,Human_RBP_ID_22076883,Human_RBP_ID_22743086,Human_RBP_ID_22996919,Human_RBP_ID_23115003,Human_RBP_ID_23119355,Human_RBP_ID_23856671,Human_RBP_ID_24545951,Human_RBP_ID_26338841,Human_RBP_ID_27478262,Human_RBP_ID_27818061 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 114411 RMVar_ID_114411 Human_SNP_ID_838509932 m1A Human chr2 - 112647703 112647703 112647703 ATGGAGGATGAATGCACGAACCAGGAAGAATAAAATTCCAGACATAATTCCAGAAAGCAGTGGGG ATGGAGGATGAATGCACGAACCAGGAAGAATACAATTCCAGACATAATTCCAGAAAGCAGTGGGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:112647396..112647704 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114412 RMVar_ID_114412 Human_SNP_ID_838520166 m1A Human chr2 + 158642508 158642508 158642508 TTCATTCTAGGTGTGTAGGTTAGGGGGAATCAAGCATCTGGTTGACCTTCTGGACCACAGAGTTT TTCATTCTAGGTGTGTAGGTTAGGGGGAATCAGGCATCTGGTTGACCTTCTGGACCACAGAGTTT A G PKP4 Ensembl:ENSG00000144283 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:158634097..158642510 32194978 MeRIP-seq:(Medium) rs750922618 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 3 liver Human_RBP_ID_5528056,Human_RBP_ID_8843167,Human_RBP_ID_17504081,Human_RBP_ID_17964222,Human_RBP_ID_22076662,Human_RBP_ID_25575700 Human_Splice_Rec_311788,Human_Splice_Rec_311826,Human_Splice_Rec_311864,Human_Splice_Rec_311900,Human_Splice_Rec_311948,Human_Splice_Rec_311982 Human_miRNA_ID_1423875,Human_miRNA_ID_2727209 RMVar_hsa_circ_115220,RMVar_hsa_circ_107361,RMVar_hsa_circ_32929,RMVar_hsa_circ_372184,RMVar_hsa_circ_203988,RMVar_hsa_circ_203987,RMVar_hsa_circ_347654,RMVar_hsa_circ_268617,RMVar_hsa_circ_35084,RMVar_hsa_circ_75189,RMVar_hsa_circ_203998,RMVar_hsa_circ_203999,RMVar_hsa_circ_275646,RMVar_hsa_circ_94303,RMVar_hsa_circ_204002,RMVar_hsa_circ_204003,RMVar_hsa_circ_354610,RMVar_hsa_circ_334599,RMVar_hsa_circ_366422 114413 RMVar_ID_114413 Human_SNP_ID_838563521 m1A Human chr2 - 201381076 201381076 201381076 ACCGACGAGATTCCACTACAACCTTCAGTAGCACCATGAGCTTGGCCAAACTTCTACAAGAGCGA ACCGACGAGATTCCACTACAACCTTCAGTAGCGCCATGAGCTTGGCCAAACTTCTACAAGAGCGA T C TRAK2 Ensembl:ENSG00000115993 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:201380970..201381125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_143124 RMVar_hsa_circ_94151,RMVar_hsa_circ_115027,RMVar_hsa_circ_124257,RMVar_hsa_circ_205894,RMVar_hsa_circ_205895,RMVar_hsa_circ_205896 114414 RMVar_ID_114414 Human_SNP_ID_838572313 m1A Human chr2 - 235803029 235803029 235803029 CCACCATCACCACAACCATCATCACCATCACAACCATCACCACCATCACAACCACAACCATCACC CCACCATCACCACAACCATCATCACCATCACAGCCATCACCACCATCACAACCACAACCATCACC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:235802610..235803225;chr2:235802630..235803189 26863196 MeRIP-seq:(Medium) rs760484700 Functional Loss SNV ICGC 33..33 33 MELA 1 - 114415 RMVar_ID_114415 Human_SNP_ID_838582083 m1A Human chr2 - 173963833 173963833 173963833 CTCGCTCTGCTGGCCGCTACCTGCAGCAAGATAGGGCCGCCATCGCCGGGCGACGACGAGGAGGA CTCGCTCTGCTGGCCGCTACCTGCAGCAAGATGGGGCCGCCATCGCCGGGCGACGACGAGGAGGA T C SP3 Ensembl:ENSG00000172845 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:173963364..173965304 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck Human_RBP_ID_538196,Human_RBP_ID_4587135,Human_RBP_ID_9387688,Human_RBP_ID_18749718,Human_RBP_ID_24553147 Human_Splice_Rec_325136,Human_Splice_Rec_325137,Human_Splice_Rec_325145,Human_Splice_Rec_325163,Human_Splice_Rec_325180,Human_Splice_Rec_325181 RMVar_hsa_circ_25580 114416 RMVar_ID_114416 Human_SNP_ID_838586470 m1A Human chr2 + 174337471 174337471 174337471 GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG GCCGCCCGGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCCTCCGCGGG A G SP9 Ensembl:ENSG00000217236 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:174337450..174337569 26863196 MeRIP-seq:(Medium) rs368984751 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,CHOL 2 head and neck Human_RBP_ID_4587249 114417 RMVar_ID_114417 Human_SNP_ID_838601917 m1A Human chr2 - 231455459 231455459 231455459 CGTGGTGGAGGCAGAGGCGGCTTTGGAGGACGAGGTGGTGGTAGAGGAGGCCGAGGAGGATTTGG CGTGGTGGAGGCAGAGGCGGCTTTGGAGGACGCGGTGGTGGTAGAGGAGGCCGAGGAGGATTTGG T G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:231455012..231455624;chr2:231454976..231455626;chr2:231454967..231455630;chr2:231454969..231455625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_545705,Human_RBP_ID_774976,Human_RBP_ID_828392,Human_RBP_ID_1022244,Human_RBP_ID_1067771,Human_RBP_ID_3617987,Human_RBP_ID_4599419,Human_RBP_ID_6895025,Human_RBP_ID_8513762,Human_RBP_ID_8846300,Human_RBP_ID_9296973,Human_RBP_ID_9353841,Human_RBP_ID_17658270,Human_RBP_ID_17952169,Human_RBP_ID_22450104,Human_RBP_ID_23132780,Human_RBP_ID_23856607,Human_RBP_ID_24488476,Human_RBP_ID_26338818,Human_RBP_ID_27287445,Human_RBP_ID_27478230 Human_Splice_Rec_369925,Human_Splice_Rec_369949 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_377381,RMVar_hsa_circ_207584 114418 RMVar_ID_114418 Human_SNP_ID_838635119 m1A Human chr2 + 27026377 27026377 27026377 CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACAGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC CTGAGGGCGGCCGCAGCCCTGGCTGACTGCACGGCTTCCCCGTGCCTCCCTCCCTGCTCCACTCC A G MAPRE3 Ensembl:ENSG00000084764 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3754733 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,COCA,central_nervous_system astrocytoma_Grade_III,large_intestine adenocarcinoma 10 large intestine,brain Human_RBP_ID_27816894 Human_Splice_Rec_226552,Human_Splice_Rec_226564,Human_Splice_Rec_226590,Human_Splice_Rec_226616 GWAS_ID_11541,GWAS_ID_11542,GWAS_ID_11543,GWAS_ID_11544,GWAS_ID_11545,GWAS_ID_11546,GWAS_ID_11547,GWAS_ID_11548,GWAS_ID_11549,GWAS_ID_11550,GWAS_ID_11551,GWAS_ID_11552,GWAS_ID_11553,GWAS_ID_11554,GWAS_ID_11555,GWAS_ID_11556,GWAS_ID_11557,GWAS_ID_11558,GWAS_ID_11559,GWAS_ID_11560,GWAS_ID_11561 114419 RMVar_ID_114419 Human_SNP_ID_838635395 m1A Human chr2 + 85303913 85303913 85303913 CTCTTTGGAAGCAGGAATCCCCCGGCCCCCTCACCCATCCGAGCTGTCACCGTATTACCCACTCT CTCTTTGGAAGCAGGAATCCCCCGGCCCCCTCCCCCATCCGAGCTGTCACCGTATTACCCACTCT A C TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:85303876..85303993 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_Splice_Rec_267902,Human_Splice_Rec_267903,Human_Splice_Rec_267927 RMVar_hsa_circ_8045 114420 RMVar_ID_114420 Human_SNP_ID_838644376 m1A Human chr2 - 196793037 196793037 196793037 GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAAGAAACACCTGAGCAACCCACTGCGGGCGATGT GAGGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAAACACCTGAGCAACCCACTGCGGGCGATGT T C GTF3C3 Ensembl:ENSG00000119041 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:196792929..196793182 26863196 MeRIP-seq:(Medium) rs1431679197 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,LICA,liver neoplasm 6 liver,stomach Human_RBP_ID_58340,Human_RBP_ID_242651,Human_RBP_ID_829972,Human_RBP_ID_923706,Human_RBP_ID_9385238,Human_RBP_ID_21982413,Human_RBP_ID_22997213,Human_RBP_ID_24546546,Human_RBP_ID_26340188,Human_RBP_ID_27817894 Human_Splice_Rec_341327,Human_Splice_Rec_341361,Human_Splice_Rec_341417,Human_Splice_Rec_341443 RMVar_hsa_circ_98334,RMVar_hsa_circ_46649,RMVar_hsa_circ_205547,RMVar_hsa_circ_23316,RMVar_hsa_circ_61581,RMVar_hsa_circ_276527,RMVar_hsa_circ_205555,RMVar_hsa_circ_74775 114421 RMVar_ID_114421 Human_SNP_ID_838655253 m1A Human chr2 + 136115059 136115059 136115059 GGATGGGGTTCAGACAACAGTGGAAGAAAGCTAGGGCCTCGGTGATGGAAATCCACTTGTGCACA GGATGGGGTTCAGACAACAGTGGAAGAAAGCTTGGGCCTCGGTGATGGAAATCCACTTGTGCACA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:136115011..136115259 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,lymph_node diffuse_large_B_cell_lymphoma 2 haematopoietic and lymphoid tissue 114422 RMVar_ID_114422 Human_SNP_ID_838663225 m1A Human chr2 + 135135710 135135710 135135710 GTGCCAGATAATCTAAAAGAAACAGATAAGGAAAAGGGAGAGGTAGGAAAATCTTGGGATTCCTG GTGCCAGATAATCTAAAAGAAACAGATAAGGACAAGGGAGAGGTAGGAAAATCTTGGGATTCCTG A C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:135135659..135135797 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_534816,Human_RBP_ID_4582296,Human_RBP_ID_24546154,Human_RBP_ID_27818939 RMVar_hsa_circ_16664,RMVar_hsa_circ_58022,RMVar_hsa_circ_311022,RMVar_hsa_circ_349904,RMVar_hsa_circ_303978,RMVar_hsa_circ_203369,RMVar_hsa_circ_203368,RMVar_hsa_circ_203374,RMVar_hsa_circ_27431,RMVar_hsa_circ_203378,RMVar_hsa_circ_293723,RMVar_hsa_circ_346358,RMVar_hsa_circ_203379,RMVar_hsa_circ_370340,RMVar_hsa_circ_289131,RMVar_hsa_circ_32206,RMVar_hsa_circ_203381,RMVar_hsa_circ_330549,RMVar_hsa_circ_338356,RMVar_hsa_circ_203382,RMVar_hsa_circ_301742,RMVar_hsa_circ_268159,RMVar_hsa_circ_203384,RMVar_hsa_circ_68535 114423 RMVar_ID_114423 Human_SNP_ID_838666656 m1A Human chr2 + 132266774 132266774 132266774 AGAGAGAGATAGACAGACAGGCAGAGAAAGACAGTAAGACAGAAGACAGACAAAGAGAGAGAGAG AGAGAGAGATAGACAGACAGGCAGAGAAAGACGGTAAGACAGAAGACAGACAAAGAGAGAGAGAG A G lnc-GPR39-10,lnc-GPR39-10:2 RNACentral:URS0000D5BB06,RNACentral:URS0000D59EB8 lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:132266764..132266829 26863196 MeRIP-seq:(Medium) rs1027947805 Functional Loss SNV ICGC 33..33 33 COCA 1 - 114424 RMVar_ID_114424 Human_SNP_ID_838720561 m1A Human chr2 + 128318491 128318491 128318491 GTACTGGTACAAGATGAGCATGAAGCACACCGAGCCCGCCACCACCAGCACGAACTTGCTGGCGC GTACTGGTACAAGATGAGCATGAAGCACACCGGGCCCGCCACCACCAGCACGAACTTGCTGGCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr2:128318316..128318589;chr2:128318301..128318606 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114425 RMVar_ID_114425 Human_SNP_ID_838725544 m1A Human chr2 - 231457726 231457726 231457726 AACCTTTGAAGAAAAGCAGGGAACAGAGATCGATGGGCGATCTATTTCCCTGTACTATACTGGAG AACCTTTGAAGAAAAGCAGGGAACAGAGATCGTTGGGCGATCTATTTCCCTGTACTATACTGGAG T A NCL Ensembl:ENSG00000115053 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231457676..231457823 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_545734,Human_RBP_ID_1584199,Human_RBP_ID_1912520,Human_RBP_ID_3618002,Human_RBP_ID_4599458,Human_RBP_ID_5194516,Human_RBP_ID_6895062,Human_RBP_ID_8846329,Human_RBP_ID_9385603,Human_RBP_ID_13794648,Human_RBP_ID_17275380,Human_RBP_ID_17699989,Human_RBP_ID_17952181,Human_RBP_ID_18315308,Human_RBP_ID_18544609,Human_RBP_ID_18755746,Human_RBP_ID_22006104,Human_RBP_ID_24378921,Human_RBP_ID_26338830,Human_RBP_ID_26664031,Human_RBP_ID_27007763,Human_RBP_ID_27818044 Human_Splice_Rec_369916,Human_Splice_Rec_369917,Human_Splice_Rec_369940,Human_Splice_Rec_369941,Human_Splice_Rec_369952,Human_Splice_Rec_369953,Human_Splice_Rec_369976 Human_miRNA_ID_2349333 RMVar_hsa_circ_61891,RMVar_hsa_circ_69694,RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_207585,RMVar_hsa_circ_112851,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207590,RMVar_hsa_circ_75733,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587 114426 RMVar_ID_114426 Human_SNP_ID_838749926 m1A Human chr2 + 55233376 55233376 55233376 TTCACTTTAACACTCATAGGTTGAACCCTCGGATACGATAGAAAATGTAAAGGCCAAGATCCAGG TTCACTTTAACACTCATAGGTTGAACCCTCGGTTACGATAGAAAATGTAAAGGCCAAGATCCAGG A T RPS27A Ensembl:ENSG00000143947 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:55233351..55233425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_242907,Human_RBP_ID_921935,Human_RBP_ID_4623313,Human_RBP_ID_9108832,Human_RBP_ID_13917654,Human_RBP_ID_22451281,Human_RBP_ID_23211550,Human_RBP_ID_26818471 Human_Splice_Rec_246594,Human_Splice_Rec_246602,Human_Splice_Rec_246610,Human_Splice_Rec_246614,Human_Splice_Rec_246618,Human_Splice_Rec_246628,Human_Splice_Rec_246632,Human_Splice_Rec_246636,Human_Splice_Rec_246638 RMVar_hsa_circ_199981,RMVar_hsa_circ_315327,RMVar_hsa_circ_369810,RMVar_hsa_circ_199983,RMVar_hsa_circ_77479,RMVar_hsa_circ_199982 114427 RMVar_ID_114427 Human_SNP_ID_838756328 m1A Human chr2 - 85327246 85327246 85327246 AACAGGTCGGGTGCGGAGGCAAAGACCCAAAAAGACAGCCCTAGCAAGTCAGGTTCGGAGGCGCA AACAGGTCGGGTGCGGAGGCAAAGACCCAAAAGGACAGCCCTAGCAAGTCAGGTTCGGAGGCGCA T C TGOLN2 Ensembl:ENSG00000152291 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:85326948..85327550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_778268,Human_RBP_ID_1197085,Human_RBP_ID_4618091 RMVar_hsa_circ_53992 114428 RMVar_ID_114428 Human_SNP_ID_838797429 m1A Human chr2 + 747936 747936 747936 TCACCATCACCACCACCAATGACAATGACATCACAGCCCCGACCTCACCATCACCACCACCAATG TCACCATCACCACCACCAATGACAATGACATCCCAGCCCCGACCTCACCATCACCACCACCAATG A C AC116609.2 Ensembl:ENSG00000231173 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:747721..748184 26863196 MeRIP-seq:(Medium) rs376461937 Functional Loss SNV ICGC 33..33 33 LICA 1 - 114429 RMVar_ID_114429 Human_SNP_ID_838856979 m1A Human chr2 - 231455244 231455244 231455244 CTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCAGAGGAGGAGGAGGTGACCACAAGCCACAAGGA CTCCTGTAGGGCGAGGAGGCTTCCGAGGAGGCCGAGGAGGAGGAGGTGACCACAAGCCACAAGGA T G NCL Ensembl:ENSG00000115053 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:231454975..231456725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_242380,Human_RBP_ID_545701,Human_RBP_ID_774974,Human_RBP_ID_829693,Human_RBP_ID_922594,Human_RBP_ID_1068038,Human_RBP_ID_4599413,Human_RBP_ID_6895021,Human_RBP_ID_17657922,Human_RBP_ID_22076871,Human_RBP_ID_22452012,Human_RBP_ID_23132777,Human_RBP_ID_24546238,Human_RBP_ID_26340333,Human_RBP_ID_27819358 Human_Splice_Rec_369926,Human_Splice_Rec_369950 Human_miRNA_ID_2014995 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583 114430 RMVar_ID_114430 Human_SNP_ID_838866701 m1A Human chr2 - 15603267 15603267 15603267 TTCAGTTATTTTAGAAACACTTACCTAGGTCCAAAGAGGCCTGCATGGTAGACCACCCGACCCTG TTCAGTTATTTTAGAAACACTTACCTAGGTCCGAAGAGGCCTGCATGGTAGACCACCCGACCCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:15603176..15603304 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 4 uterus 114431 RMVar_ID_114431 Human_SNP_ID_838894229 m1A Human chr2 - 226795698 226795698 226795698 CACCTCGCCAGCTGCCCCTGTAAGCTATGCTGACATGCGAACAGGCATTGCTGCAGAGGAGGTGA CACCTCGCCAGCTGCCCCTGTAAGCTATGCTGGCATGCGAACAGGCATTGCTGCAGAGGAGGTGA T C IRS1 Ensembl:ENSG00000169047 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:226795479..226796027 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 OV,large_intestine adenocarcinoma 2 large intestine 114432 RMVar_ID_114432 Human_SNP_ID_838908183 m1A Human chr2 - 3519462 3519462 3519462 GCGCGTCATGGTGCAGGCCTGGTATATGGACGACGCCCCGGGCGACCCGCGGCAACCCCACCGCC GCGCGTCATGGTGCAGGCCTGGTATATGGACGGCGCCCCGGGCGACCCGCGGCAACCCCACCGCC T C ADI1 Ensembl:ENSG00000182551 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:3519351..3519550 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_550002,Human_RBP_ID_774184,Human_RBP_ID_4623073,Human_RBP_ID_9383033,Human_RBP_ID_17658312,Human_RBP_ID_22450987,Human_RBP_ID_27839980 Human_Splice_Rec_213081 114433 RMVar_ID_114433 Human_SNP_ID_838925047 m1A Human chr2 - 211774685 211774685 211774685 GAAATTGGCAAATCTTACCTTGCCTGTTTACCAAAAACACCACCTCTAGCATTATCAGTATTAGA GAAATTGGCAAATCTTACCTTGCCTGTTTACCGAAAACACCACCTCTAGCATTATCAGTATTAGA T C ERBB4 Ensembl:ENSG00000178568 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr2:211774475..211774704;chr2:211774432..211774719;chr2:211774479..211774686 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_7889,RMVar_hsa_circ_16062,RMVar_hsa_circ_44323,RMVar_hsa_circ_338799,RMVar_hsa_circ_4049,RMVar_hsa_circ_20704,RMVar_hsa_circ_38482,RMVar_hsa_circ_29306,RMVar_hsa_circ_320170,RMVar_hsa_circ_322285,RMVar_hsa_circ_13551,RMVar_hsa_circ_36600,RMVar_hsa_circ_52961,RMVar_hsa_circ_206602,RMVar_hsa_circ_335292,RMVar_hsa_circ_346581,RMVar_hsa_circ_206601 114434 RMVar_ID_114434 Human_SNP_ID_838927953 m1A Human chr2 + 6917531 6917516 6917532 GTGCGGGCCGTGCGGGCTGCGCGGGCGCGGGGAGGCGCGGGCGGCAAACTGCGGGCACCCGGCAC GTGCGGGCCGTGCGGGCT________________GCGCGGGCGGCAAACTGCGGGCACCCGGCAC TGCGCGGGCGCGGGGAG T RNF144A Ensembl:ENSG00000151692 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:6917480..6917600 26863196 MeRIP-seq:(Medium) rs527528919 Functional Loss DEL ICGC 19..34 33 PBCA 1 - Human_RBP_ID_4622170,Human_RBP_ID_18422086 Human_Splice_Rec_214861,Human_Splice_Rec_214875 114435 RMVar_ID_114435 Human_SNP_ID_838942777 m1A Human chr2 + 218403329 218403329 218403329 GTCCTGCGTCTTCCACCGGGGGAACTACGTGAAGGACCTGAGCCGGTTGGGTCGAGACCTGCGGC GTCCTGCGTCTTCCACCGGGGGAACTACGTGATGGACCTGAGCCGGTTGGGTCGAGACCTGCGGC A T CTDSP1 Ensembl:ENSG00000144579 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:218403092..218403396 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_243016,Human_RBP_ID_9387945,Human_RBP_ID_19002956,Human_RBP_ID_23853353 Human_Splice_Rec_358726,Human_Splice_Rec_358727,Human_Splice_Rec_358738,Human_Splice_Rec_358739,Human_Splice_Rec_358752,Human_Splice_Rec_358764,Human_Splice_Rec_358774,Human_Splice_Rec_358775,Human_Splice_Rec_358786,Human_Splice_Rec_358802,Human_Splice_Rec_358803,Human_Splice_Rec_358814,Human_Splice_Rec_358815,Human_Splice_Rec_358832,Human_Splice_Rec_358833,Human_Splice_Rec_358842,Human_Splice_Rec_358852,Human_Splice_Rec_358853 Human_miRNA_ID_2268543,Human_miRNA_ID_2888461 RMVar_hsa_circ_96993,RMVar_hsa_circ_268733,RMVar_hsa_circ_206917,RMVar_hsa_circ_120609,RMVar_hsa_circ_206920,RMVar_hsa_circ_115103,RMVar_hsa_circ_125268,RMVar_hsa_circ_206922,RMVar_hsa_circ_206923 114436 RMVar_ID_114436 Human_SNP_ID_838950064 m1A Human chr2 + 85354491 85354491 85354491 GGACGGCCAGCAGCAGCACAGCCAGGAGCAGCACCAGCGGAAGCCACATCACGCCGGCGTCGGGT GGACGGCCAGCAGCAGCACAGCCAGGAGCAGCGCCAGCGGAAGCCACATCACGCCGGCGTCGGGT A G ELMOD3 Ensembl:ENSG00000115459 Protein coding exon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr2:85354397..85354505 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 114437 RMVar_ID_114437 Human_SNP_ID_838984712 m1A Human chr2 + 101860902 101860902 101860902 CAGTCTAAGCAGACAGGCAGAGTATTGGAGCCACCAGTGCCTTCCCGATCAGAGTCTTTTTCCAA CAGTCTAAGCAGACAGGCAGAGTATTGGAGCCGCCAGTGCCTTCCCGATCAGAGTCTTTTTCCAA A G MAP4K4 Ensembl:ENSG00000071054 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:101860895..101861045 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 11 brain Human_RBP_ID_21932351 Human_Splice_Rec_281796,Human_Splice_Rec_281797,Human_Splice_Rec_281970,Human_Splice_Rec_281971,Human_Splice_Rec_282194,Human_Splice_Rec_282195,Human_Splice_Rec_282300,Human_Splice_Rec_282301,Human_Splice_Rec_282404,Human_Splice_Rec_282405,Human_Splice_Rec_282474,Human_Splice_Rec_282475 RMVar_hsa_circ_70658,RMVar_hsa_circ_97038,RMVar_hsa_circ_202260,RMVar_hsa_circ_116064,RMVar_hsa_circ_202264,RMVar_hsa_circ_315560,RMVar_hsa_circ_9734,RMVar_hsa_circ_17741,RMVar_hsa_circ_66397,RMVar_hsa_circ_361600,RMVar_hsa_circ_53472,RMVar_hsa_circ_22934,RMVar_hsa_circ_43332,RMVar_hsa_circ_39473 114438 RMVar_ID_114438 Human_SNP_ID_839001371 m1A Human chr2 - 96296982 96296982 96296982 CAAAACACTGAATCGGATCCAGAGTAAGCTCTACCGTGCTGCCCTTGAGACGGATGAGAATCTGC CAAAACACTGAATCGGATCCAGAGTAAGCTCTGCCGTGCTGCCCTTGAGACGGATGAGAATCTGC T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:96296905..96297009 26863196 MeRIP-seq:(Medium) rs1259944697 Functional Loss SNV TCGA 33..33 33 ACC 1 - Human_RBP_ID_305707,Human_RBP_ID_4635469,Human_RBP_ID_5195319,Human_RBP_ID_5589687,Human_RBP_ID_8527333,Human_RBP_ID_8850820 Human_Splice_Rec_274842,Human_Splice_Rec_274843,Human_Splice_Rec_275022,Human_Splice_Rec_275023 Human_miRNA_ID_2780625,Human_miRNA_ID_2786193 RMVar_hsa_circ_79633,RMVar_hsa_circ_88869,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_201844,RMVar_hsa_circ_201845,RMVar_hsa_circ_84091,RMVar_hsa_circ_201865,RMVar_hsa_circ_98292,RMVar_hsa_circ_78669,RMVar_hsa_circ_46281,RMVar_hsa_circ_201866,RMVar_hsa_circ_77402,RMVar_hsa_circ_201867,RMVar_hsa_circ_115047,RMVar_hsa_circ_75633,RMVar_hsa_circ_201869,RMVar_hsa_circ_201870,RMVar_hsa_circ_92734,RMVar_hsa_circ_201874,RMVar_hsa_circ_201873,RMVar_hsa_circ_43933 114439 RMVar_ID_114439 Human_SNP_ID_839005708 m1A Human chr2 + 148020703 148020703 148020703 TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGACTTCACCTGCCGCTGCGGACCGTACACAACCA TCACCGAATCGCCTGGCCGCGTCCTCTGCTAGGCTTCACCTGCCGCTGCGGACCGTACACAACCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:148020670..148021604 26863196 MeRIP-seq:(Medium) rs897172 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,frontal_lobe astrocytoma_Grade_III,COCA,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_II 11 brain Clinvar_Rec_425,Clinvar_Rec_3738 GWAS_ID_9628,GWAS_ID_9629,GWAS_ID_9630,GWAS_ID_9631,GWAS_ID_9632,GWAS_ID_9633,GWAS_ID_9634,GWAS_ID_9635,GWAS_ID_9636,GWAS_ID_9637,GWAS_ID_9638,GWAS_ID_9639,GWAS_ID_9640,GWAS_ID_9641,GWAS_ID_9642,GWAS_ID_9643,GWAS_ID_9644,GWAS_ID_9645,GWAS_ID_9646,GWAS_ID_9647,GWAS_ID_9648,GWAS_ID_9649,GWAS_ID_9650,GWAS_ID_9651,GWAS_ID_9652,GWAS_ID_9653,GWAS_ID_9654,GWAS_ID_9655,GWAS_ID_9656,GWAS_ID_9657,GWAS_ID_9658,GWAS_ID_9659,GWAS_ID_9660,GWAS_ID_9661,GWAS_ID_9662,GWAS_ID_9663,GWAS_ID_9664,GWAS_ID_9665,GWAS_ID_9666,GWAS_ID_9667,GWAS_ID_9668,GWAS_ID_9669,GWAS_ID_9670,GWAS_ID_9671,GWAS_ID_9672,GWAS_ID_9673,GWAS_ID_9674,GWAS_ID_9675,GWAS_ID_9676,GWAS_ID_9677,GWAS_ID_9678,GWAS_ID_9679,GWAS_ID_9680,GWAS_ID_9681,GWAS_ID_9682,GWAS_ID_9683,GWAS_ID_9684,GWAS_ID_9685,GWAS_ID_9686,GWAS_ID_9687,GWAS_ID_9688,GWAS_ID_9689,GWAS_ID_9690,GWAS_ID_9691,GWAS_ID_9692,GWAS_ID_9693,GWAS_ID_9694,GWAS_ID_9695,GWAS_ID_9696,GWAS_ID_9697,GWAS_ID_9698,GWAS_ID_9699,GWAS_ID_9700,GWAS_ID_9701,GWAS_ID_9702,GWAS_ID_9703,GWAS_ID_9704,GWAS_ID_9705,GWAS_ID_9706,GWAS_ID_9707,GWAS_ID_9708,GWAS_ID_9709,GWAS_ID_9710,GWAS_ID_9711,GWAS_ID_9712,GWAS_ID_9713,GWAS_ID_9714,GWAS_ID_9715,GWAS_ID_9716,GWAS_ID_9717,GWAS_ID_9718,GWAS_ID_9719,GWAS_ID_9720,GWAS_ID_9721,GWAS_ID_9722,GWAS_ID_9723,GWAS_ID_9724,GWAS_ID_9725,GWAS_ID_9726,GWAS_ID_9727,GWAS_ID_9728,GWAS_ID_9729,GWAS_ID_9730,GWAS_ID_9731,GWAS_ID_9732,GWAS_ID_9733,GWAS_ID_9734,GWAS_ID_9735,GWAS_ID_9736,GWAS_ID_9737,GWAS_ID_9738,GWAS_ID_9739,GWAS_ID_9740,GWAS_ID_9741,GWAS_ID_9742,GWAS_ID_9743,GWAS_ID_9744,GWAS_ID_9745,GWAS_ID_9746,GWAS_ID_9747,GWAS_ID_9748,GWAS_ID_9749,GWAS_ID_9750,GWAS_ID_9751,GWAS_ID_9752,GWAS_ID_9753,GWAS_ID_9754,GWAS_ID_9755,GWAS_ID_9756,GWAS_ID_9757,GWAS_ID_9758,GWAS_ID_9759,GWAS_ID_9760,GWAS_ID_9761,GWAS_ID_9762,GWAS_ID_9763,GWAS_ID_9764,GWAS_ID_9765,GWAS_ID_9766,GWAS_ID_9767,GWAS_ID_9768,GWAS_ID_9769,GWAS_ID_9770,GWAS_ID_9771,GWAS_ID_9772,GWAS_ID_9773,GWAS_ID_9774,GWAS_ID_9775,GWAS_ID_9776,GWAS_ID_9777,GWAS_ID_9778,GWAS_ID_9779,GWAS_ID_9780,GWAS_ID_9781,GWAS_ID_9782,GWAS_ID_9783,GWAS_ID_9784,GWAS_ID_9785,GWAS_ID_9786,GWAS_ID_9787,GWAS_ID_9788,GWAS_ID_9789,GWAS_ID_9790,GWAS_ID_9791,GWAS_ID_9792,GWAS_ID_9793,GWAS_ID_9794,GWAS_ID_9795,GWAS_ID_9796,GWAS_ID_9797,GWAS_ID_9798,GWAS_ID_9799,GWAS_ID_9800,GWAS_ID_9801,GWAS_ID_9802,GWAS_ID_9803,GWAS_ID_9804,GWAS_ID_9805,GWAS_ID_9806,GWAS_ID_9807,GWAS_ID_9808,GWAS_ID_9809,GWAS_ID_9810,GWAS_ID_9811,GWAS_ID_9812,GWAS_ID_9813,GWAS_ID_9814,GWAS_ID_9815,GWAS_ID_9816,GWAS_ID_9817,GWAS_ID_9818,GWAS_ID_9819,GWAS_ID_9820,GWAS_ID_9821,GWAS_ID_9822,GWAS_ID_9823,GWAS_ID_9824,GWAS_ID_9825,GWAS_ID_9826,GWAS_ID_9827,GWAS_ID_9828,GWAS_ID_9829,GWAS_ID_9830,GWAS_ID_9831,GWAS_ID_9832,GWAS_ID_9833,GWAS_ID_9834,GWAS_ID_9835,GWAS_ID_9836,GWAS_ID_9837,GWAS_ID_9838,GWAS_ID_9839,GWAS_ID_9840,GWAS_ID_9841,GWAS_ID_9842,GWAS_ID_9843,GWAS_ID_9844,GWAS_ID_9845,GWAS_ID_9846,GWAS_ID_9847,GWAS_ID_9848,GWAS_ID_9849,GWAS_ID_9850,GWAS_ID_9851,GWAS_ID_9852,GWAS_ID_9853,GWAS_ID_9854,GWAS_ID_9855,GWAS_ID_9856,GWAS_ID_9857,GWAS_ID_9858,GWAS_ID_9859,GWAS_ID_9860,GWAS_ID_9861,GWAS_ID_9862,GWAS_ID_9863,GWAS_ID_9864,GWAS_ID_9865,GWAS_ID_9866,GWAS_ID_9867,GWAS_ID_9868,GWAS_ID_9869,GWAS_ID_9870,GWAS_ID_9871,GWAS_ID_9872,GWAS_ID_9873,GWAS_ID_9874,GWAS_ID_9875,GWAS_ID_9876,GWAS_ID_9877,GWAS_ID_9878,GWAS_ID_9879,GWAS_ID_9880,GWAS_ID_9881,GWAS_ID_9882,GWAS_ID_9883,GWAS_ID_9884,GWAS_ID_9885,GWAS_ID_9886,GWAS_ID_9887,GWAS_ID_9888,GWAS_ID_9889,GWAS_ID_9890,GWAS_ID_9891,GWAS_ID_9892,GWAS_ID_9893,GWAS_ID_9894,GWAS_ID_9895,GWAS_ID_9896,GWAS_ID_9897,GWAS_ID_9898,GWAS_ID_9899,GWAS_ID_9900,GWAS_ID_9901,GWAS_ID_9902,GWAS_ID_9903,GWAS_ID_9904,GWAS_ID_9905,GWAS_ID_9906,GWAS_ID_9907,GWAS_ID_9908,GWAS_ID_9909,GWAS_ID_9910,GWAS_ID_9911,GWAS_ID_9912,GWAS_ID_9913,GWAS_ID_9914,GWAS_ID_9915,GWAS_ID_9916,GWAS_ID_9917,GWAS_ID_9918,GWAS_ID_9919,GWAS_ID_9920,GWAS_ID_9921,GWAS_ID_9922,GWAS_ID_9923,GWAS_ID_9924,GWAS_ID_9925,GWAS_ID_9926,GWAS_ID_9927,GWAS_ID_9928,GWAS_ID_9929,GWAS_ID_9930,GWAS_ID_9931,GWAS_ID_9932,GWAS_ID_9933,GWAS_ID_9934,GWAS_ID_9935,GWAS_ID_9936,GWAS_ID_9937,GWAS_ID_9938,GWAS_ID_9939,GWAS_ID_9940,GWAS_ID_9941,GWAS_ID_9942,GWAS_ID_9943,GWAS_ID_9944,GWAS_ID_9945,GWAS_ID_9946,GWAS_ID_9947,GWAS_ID_9948,GWAS_ID_9949,GWAS_ID_9950,GWAS_ID_9951,GWAS_ID_9952,GWAS_ID_9953,GWAS_ID_9954,GWAS_ID_9955,GWAS_ID_9956,GWAS_ID_9957,GWAS_ID_9958,GWAS_ID_9959,GWAS_ID_9960,GWAS_ID_9961,GWAS_ID_9962,GWAS_ID_9963,GWAS_ID_9964,GWAS_ID_9965,GWAS_ID_9966,GWAS_ID_9967,GWAS_ID_9968,GWAS_ID_9969,GWAS_ID_9970,GWAS_ID_9971,GWAS_ID_9972,GWAS_ID_9973,GWAS_ID_9974,GWAS_ID_9975,GWAS_ID_9976,GWAS_ID_9977,GWAS_ID_9978,GWAS_ID_9979,GWAS_ID_9980,GWAS_ID_9981,GWAS_ID_9982,GWAS_ID_9983,GWAS_ID_9984,GWAS_ID_9985,GWAS_ID_9986,GWAS_ID_9987,GWAS_ID_9988,GWAS_ID_9989,GWAS_ID_9990,GWAS_ID_9991,GWAS_ID_9992,GWAS_ID_9993,GWAS_ID_9994,GWAS_ID_9995,GWAS_ID_9996,GWAS_ID_9997,GWAS_ID_9998,GWAS_ID_9999,GWAS_ID_10000,GWAS_ID_10001,GWAS_ID_10002,GWAS_ID_10003,GWAS_ID_10004,GWAS_ID_10005,GWAS_ID_10006,GWAS_ID_10007,GWAS_ID_10008 114440 RMVar_ID_114440 Human_SNP_ID_839007173 m1A Human chr2 + 85302550 85302542 85302551 ACATGCATCCGCTGACTCCCCTCATCACCTACAGCAATGACCACTTCTCCCCCGGCTCCCCTCCC ACATGCATCCGCTGACTCCCCTCAT_________CAATGACCACTTCTCCCCCGGCTCCCCTCCC TCACCTACAG T TCF7L1 Ensembl:ENSG00000152284 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:85302441..85302655 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 26..34 33 LICA 1 - Human_Splice_Rec_267900,Human_Splice_Rec_267901,Human_Splice_Rec_267926 RMVar_hsa_circ_8045 114441 RMVar_ID_114441 Human_SNP_ID_839054105 m1A Human chr2 - 111268261 111268260 111268262 GAAAGGAGGAAGGAAGGAAAGAAGGAAAGAAAAGAAAAAGAAAGAAAGAGAAAGGAAAAGAAAAA GAAAGGAGGAAGGAAGGAAAGAAGGAAAGAA__GAAAAAGAAAGAAAGAGAAAGGAAAAGAAAAA CTT C MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:111268193..111268319 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 ESCA 1 - Human_RBP_ID_2578901,Human_RBP_ID_25454723 RMVar_hsa_circ_80360,RMVar_hsa_circ_77921,RMVar_hsa_circ_202492,RMVar_hsa_circ_202493,RMVar_hsa_circ_101052,RMVar_hsa_circ_202495,RMVar_hsa_circ_82536,RMVar_hsa_circ_202496,RMVar_hsa_circ_106267,RMVar_hsa_circ_202497,RMVar_hsa_circ_77380,RMVar_hsa_circ_202500,RMVar_hsa_circ_46678,RMVar_hsa_circ_304253,RMVar_hsa_circ_13022,RMVar_hsa_circ_339654 114442 RMVar_ID_114442 Human_SNP_ID_839059887 m1A Human chr2 - 219574913 219574913 219574913 GGGGAGCATGGCCCAAAGACATGGGCACAGCCACGGGTCCTCCCGGTGACAGTGCCAGCAGGCCT GGGGAGCATGGCCCAAAGACATGGGCACAGCCTCGGGTCCTCCCGGTGACAGTGCCAGCAGGCCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:219572639..219574934 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 114443 RMVar_ID_114443 Human_SNP_ID_839062291 m1A Human chr2 - 186590125 186590125 186590125 GGGACGAGGGGCGCAGAGCGCGCGGGGCGGGGACAGCAGCGCAGACGGTCCTTTGCTTCCCTCCG GGGACGAGGGGCGCAGAGCGCGCGGGGCGGGGGCAGCAGCGCAGACGGTCCTTTGCTTCCCTCCG T C lnc-ZSWIM2-16 RNACentral:URS0000D585F2 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:186590074..186590171 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114444 RMVar_ID_114444 Human_SNP_ID_839073260 m1A Human chr2 + 25981374 25981374 25981374 CTCAATCTCCTTGACATTCTTGGTGACGAAGGAGGAGAGGTCCTTGATGTAGACGCCAGTCTCGG CTCAATCTCCTTGACATTCTTGGTGACGAAGGGGGAGAGGTCCTTGATGTAGACGCCAGTCTCGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:25981210..25981409 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114445 RMVar_ID_114445 Human_SNP_ID_839132668 m1A Human chr2 - 74483598 74483598 74483598 CAATTCTACCCACTTCGAGCATCTGTTACATCAGGATCATCCTCCTGATCCCCTGCCCCTCACTT CAATTCTACCCACTTCGAGCATCTGTTACATCTGGATCATCCTCCTGATCCCCTGCCCCTCACTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74483590..74483706 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114446 RMVar_ID_114446 Human_SNP_ID_839144593 m1A Human chr2 - 197500438 197500438 197500438 CCTGCAGGCCTCGGGGCCACGCGGGACTCACCATTACTCCCTCCGCCTCAGACTCGTACTCTGCT CCTGCAGGCCTCGGGGCCACGCGGGACTCACCCTTACTCCCTCCGCCTCAGACTCGTACTCTGCT T G HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Normoxia chr2:197500139..197500488;chr2:197500351..197500450;chr2:197500151..197500500;chr2:197500388..197500488 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast 114447 RMVar_ID_114447 Human_SNP_ID_839151599 m1A Human chr2 - 197497384 197497382 197497384 TCCTGTTACATTTTTTTCTTCTAGGGAAGAACAGTGATTATTGAGCAGAGTTGGGGAAGTCCCAA TCCTGTTACATTTTTTTCTTCTAGGGAAGAAC__TGATTATTGAGCAGAGTTGGGGAAGTCCCAA ACT A HSPD1 Ensembl:ENSG00000144381 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr2:197497148..197497438;chr2:197497180..197497425 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 KIRP 1 - Human_RBP_ID_776138,Human_RBP_ID_829329,Human_RBP_ID_1906815,Human_RBP_ID_2613030,Human_RBP_ID_3609753,Human_RBP_ID_5195901,Human_RBP_ID_6869259,Human_RBP_ID_8508521,Human_RBP_ID_13727771,Human_RBP_ID_22452572,Human_RBP_ID_23845931 Human_Splice_Rec_342306,Human_Splice_Rec_342326,Human_Splice_Rec_342354,Human_Splice_Rec_342368,Human_Splice_Rec_342376,Human_Splice_Rec_342384,Human_Splice_Rec_342390,Human_Splice_Rec_342394,Human_Splice_Rec_342400,Human_Splice_Rec_342406 RMVar_hsa_circ_115375,RMVar_hsa_circ_87075,RMVar_hsa_circ_205685,RMVar_hsa_circ_205686,RMVar_hsa_circ_126781,RMVar_hsa_circ_57034,RMVar_hsa_circ_205687,RMVar_hsa_circ_122492,RMVar_hsa_circ_205691,RMVar_hsa_circ_332331,RMVar_hsa_circ_205695,RMVar_hsa_circ_94462,RMVar_hsa_circ_281585,RMVar_hsa_circ_205698,RMVar_hsa_circ_345564 114448 RMVar_ID_114448 Human_SNP_ID_839206037 m1A Human chr2 - 182957477 182957477 182957477 AGGGAGAAACCAGGTGTTGAGAGCATGAGGAAAAACAGGCTGGTTGTGACCAAGTAAGTATCCAC AGGGAGAAACCAGGTGTTGAGAGCATGAGGAATAACAGGCTGGTTGTGACCAAGTAAGTATCCAC T A NCKAP1 Ensembl:ENSG00000061676 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:182957451..182957575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_918997,Human_RBP_ID_9347766,Human_RBP_ID_19102199,Human_RBP_ID_27817840 Human_Splice_Rec_334759,Human_Splice_Rec_334821 Human_miRNA_ID_2997563 RMVar_hsa_circ_7714,RMVar_hsa_circ_97415,RMVar_hsa_circ_100651,RMVar_hsa_circ_204999,RMVar_hsa_circ_116411,RMVar_hsa_circ_205002,RMVar_hsa_circ_310141,RMVar_hsa_circ_34471,RMVar_hsa_circ_205003,RMVar_hsa_circ_342232,RMVar_hsa_circ_351246,RMVar_hsa_circ_341045,RMVar_hsa_circ_306286,RMVar_hsa_circ_290891,RMVar_hsa_circ_40879,RMVar_hsa_circ_53857,RMVar_hsa_circ_8537,RMVar_hsa_circ_58616,RMVar_hsa_circ_19205,RMVar_hsa_circ_299114,RMVar_hsa_circ_205007,RMVar_hsa_circ_205008,RMVar_hsa_circ_205009,RMVar_hsa_circ_205006,RMVar_hsa_circ_101764,RMVar_hsa_circ_347028,RMVar_hsa_circ_371695,RMVar_hsa_circ_205010,RMVar_hsa_circ_348684,RMVar_hsa_circ_336797,RMVar_hsa_circ_63523,RMVar_hsa_circ_290492,RMVar_hsa_circ_35298,RMVar_hsa_circ_63256,RMVar_hsa_circ_26770,RMVar_hsa_circ_319723,RMVar_hsa_circ_205013,RMVar_hsa_circ_205015,RMVar_hsa_circ_205017,RMVar_hsa_circ_205016,RMVar_hsa_circ_205014,RMVar_hsa_circ_205011,RMVar_hsa_circ_205012,RMVar_hsa_circ_338565,RMVar_hsa_circ_378173,RMVar_hsa_circ_332348,RMVar_hsa_circ_295100,RMVar_hsa_circ_311456,RMVar_hsa_circ_315456,RMVar_hsa_circ_277669,RMVar_hsa_circ_283741,RMVar_hsa_circ_61888,RMVar_hsa_circ_19252,RMVar_hsa_circ_125239,RMVar_hsa_circ_205022,RMVar_hsa_circ_205024,RMVar_hsa_circ_205026,RMVar_hsa_circ_205025,RMVar_hsa_circ_205023,RMVar_hsa_circ_205020,RMVar_hsa_circ_205021,RMVar_hsa_circ_205030,RMVar_hsa_circ_86568,RMVar_hsa_circ_62315,RMVar_hsa_circ_205032,RMVar_hsa_circ_321513,RMVar_hsa_circ_372108,RMVar_hsa_circ_327947,RMVar_hsa_circ_317045,RMVar_hsa_circ_205033,RMVar_hsa_circ_205034,RMVar_hsa_circ_205035,RMVar_hsa_circ_93174,RMVar_hsa_circ_205036 114449 RMVar_ID_114449 Human_SNP_ID_839208653 m1A Human chr2 - 219574982 219574982 219574982 GCAGCACCAGGACGGGGTGGGTCAGCAGAGAGAGAGCAGAGGTGGCCAGGTGCAGCACGGCCCAG GCAGCACCAGGACGGGGTGGGTCAGCAGAGAGGGAGCAGAGGTGGCCAGGTGCAGCACGGCCCAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:219574826..219575075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 114450 RMVar_ID_114450 Human_SNP_ID_839245668 m1A Human chr2 - 231460764 231460764 231460764 AGCCAAGAACGTGGCTGAGGATGAAGATGAAGAAGAGGATGATGAGGACGAGGATGACGACGACG AGCCAAGAACGTGGCTGAGGATGAAGATGAAGGAGAGGATGATGAGGACGAGGATGACGACGACG T C NCL Ensembl:ENSG00000115053 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_57002,Human_RBP_ID_242384,Human_RBP_ID_774983,Human_RBP_ID_829701,Human_RBP_ID_1584232,Human_RBP_ID_1912550,Human_RBP_ID_2627049,Human_RBP_ID_3618016,Human_RBP_ID_4599478,Human_RBP_ID_5194520,Human_RBP_ID_5589079,Human_RBP_ID_6895102,Human_RBP_ID_8107524,Human_RBP_ID_8257488,Human_RBP_ID_8513813,Human_RBP_ID_8846342,Human_RBP_ID_9385636,Human_RBP_ID_9975863,Human_RBP_ID_13794781,Human_RBP_ID_17275388,Human_RBP_ID_17390555,Human_RBP_ID_17506476,Human_RBP_ID_17952195,Human_RBP_ID_18443191,Human_RBP_ID_18533503,Human_RBP_ID_22076883,Human_RBP_ID_22743086,Human_RBP_ID_22996919,Human_RBP_ID_23115003,Human_RBP_ID_23119355,Human_RBP_ID_23856671,Human_RBP_ID_24545951,Human_RBP_ID_26341809,Human_RBP_ID_27478262,Human_RBP_ID_27563645,Human_RBP_ID_27818061 Human_Splice_Rec_369907,Human_Splice_Rec_369933,Human_Splice_Rec_369967 RMVar_hsa_circ_89925,RMVar_hsa_circ_207582,RMVar_hsa_circ_80370,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_122778,RMVar_hsa_circ_118536,RMVar_hsa_circ_207588,RMVar_hsa_circ_207589,RMVar_hsa_circ_207587,RMVar_hsa_circ_88769,RMVar_hsa_circ_356333,RMVar_hsa_circ_124090,RMVar_hsa_circ_207592,RMVar_hsa_circ_207593 114451 RMVar_ID_114451 Human_SNP_ID_839247264 m1A Human chr2 + 174567919 174567919 174567919 TTTCTAATAGATGTTGATGGTGGAGGTGGGGGAGGTGCCCCAGCACTGGGCCTATCAGGAGGAAG TTTCTAATAGATGTTGATGGTGGAGGTGGGGGCGGTGCCCCAGCACTGGGCCTATCAGGAGGAAG A C AC010894.3 Ensembl:ENSG00000236449 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:174567876..174567975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 12 brain 114452 RMVar_ID_114452 Human_SNP_ID_839280393 m1A Human chr2 - 89826652 89826652 89826652 GAATGGAATGGAATCAACAAGAGTGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATG GAATGGAATGGAATCAACAAGAGTGGAATGGATTGGAATGGAATGGAATGGAATGGAATGGAATG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:89826589..89826726 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114453 RMVar_ID_114453 Human_SNP_ID_839290675 m1A Human chr2 - 32357260 32357260 32357260 GCCGAGGAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCAGCCGCCATCTTCCGGCCTGCGCTCAG GCCGAGGAGCAGCCGGGGCCCGAGGCCGCCGCCGCCGCAGCCGCCATCTTCCGGCCTGCGCTCAG T G lnc-NLRC4-4-002 RNACentral:URS00008C1097 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:32357138..32357497 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung RMVar_hsa_circ_198328 114454 RMVar_ID_114454 Human_SNP_ID_839311405 m1A Human chr2 - 47176461 47176461 47176461 GAGCTGAGTGGTTGTGTGGTCGCGTCTCGGAAACCGGTAGCGCTTGCAGCATGGTGAGTGCATCG GAGCTGAGTGGTTGTGTGGTCGCGTCTCGGAATCCGGTAGCGCTTGCAGCATGGTGAGTGCATCG T A CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding 5'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr2:47170726..47176537;chr2:47170726..47176550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_243744,Human_RBP_ID_280946,Human_RBP_ID_551915,Human_RBP_ID_777139,Human_RBP_ID_1587405,Human_RBP_ID_1918956,Human_RBP_ID_3627829,Human_RBP_ID_4610554,Human_RBP_ID_5322063,Human_RBP_ID_5502280,Human_RBP_ID_6927160,Human_RBP_ID_8520497,Human_RBP_ID_9107303,Human_RBP_ID_9330450,Human_RBP_ID_9383602,Human_RBP_ID_17963932,Human_RBP_ID_18761777,Human_RBP_ID_19097376,Human_RBP_ID_22449787,Human_RBP_ID_23133040,Human_RBP_ID_23874803,Human_RBP_ID_26339263 Human_Splice_Rec_242755,Human_Splice_Rec_242771,Human_Splice_Rec_242781,Human_Splice_Rec_242787,Human_Splice_Rec_242805,Human_Splice_Rec_242825,Human_Splice_Rec_242833,Human_Splice_Rec_242889 114455 RMVar_ID_114455 Human_SNP_ID_839311521 m1A Human chr2 - 216633582 216633582 216633582 CGCCGCCACTCGCGCCCAGTAGCAGCAGCAGCAGCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGC CGCCGCCACTCGCGCCCAGTAGCAGCAGCAGCGGCGGCAGCAGCGGCGGCGGCGGCAGCGGCAGC T C - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr2:216633421..216633655 26863410 MeRIP-seq:(Medium) rs757848711 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 114456 RMVar_ID_114456 Human_SNP_ID_839360497 m1A Human chr2 + 48440850 48440850 48440850 GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCAGGCAGATACTGCCTGACCCGTTCCCGGGAGCG GGCGGCGGCGGCGGCGGCTGCGGTGGCCAAGCGGGCAGATACTGCCTGACCCGTTCCCGGGAGCG A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:48440800..48441135 26863196 MeRIP-seq:(Medium) rs903578326 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary Human_RBP_ID_18421767 114457 RMVar_ID_114457 Human_SNP_ID_839362510 m1A Human chr2 - 27134519 27134519 27134519 TGTGAGAGGGGTAGGGAGTGCTCCCGGCGGCGACGGGGCCGAGTTCACCAGCCGCCGGGGCAGTA TGTGAGAGGGGTAGGGAGTGCTCCCGGCGGCGGCGGGGCCGAGTTCACCAGCCGCCGGGGCAGTA T C PREB Ensembl:ENSG00000138073 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27134471..27134613 26863196 MeRIP-seq:(Medium) rs1030552879 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_242841,Human_RBP_ID_775839,Human_RBP_ID_830042,Human_RBP_ID_923073,Human_RBP_ID_4622303,Human_RBP_ID_5118255,Human_RBP_ID_5146520,Human_RBP_ID_5379184,Human_RBP_ID_9330963,Human_RBP_ID_22451178 RMVar_hsa_circ_107489,RMVar_hsa_circ_197886 114458 RMVar_ID_114458 Human_SNP_ID_839413119 m1A Human chr2 + 189005364 189005364 189005364 TCATTCCTTTGTATACAGGGTGAAAGTGGGAAACCAGGAGCTAACGGTCTCAGTGGAGAACGTGG TCATTCCTTTGTATACAGGGTGAAAGTGGGAAGCCAGGAGCTAACGGTCTCAGTGGAGAACGTGG A G COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:189005351..189005400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_Splice_Rec_336344,Human_Splice_Rec_336345 Human_miRNA_ID_1542118,Human_miRNA_ID_1595471 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_114363,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205216,RMVar_hsa_circ_205219,RMVar_hsa_circ_88349,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_88829,RMVar_hsa_circ_205227,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_35268,RMVar_hsa_circ_109126,RMVar_hsa_circ_205237,RMVar_hsa_circ_107947,RMVar_hsa_circ_205239,RMVar_hsa_circ_205240,RMVar_hsa_circ_124579,RMVar_hsa_circ_205241,RMVar_hsa_circ_127071,RMVar_hsa_circ_358368 114459 RMVar_ID_114459 Human_SNP_ID_839413129 m1A Human chr2 + 189005364 189005364 189005364 TCATTCCTTTGTATACAGGGTGAAAGTGGGAAACCAGGAGCTAACGGTCTCAGTGGAGAACGTGG TCATTCCTTTGTATACAGGGTGAAAGTGGGAATCCAGGAGCTAACGGTCTCAGTGGAGAACGTGG A T COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:189005351..189005400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_Splice_Rec_336344,Human_Splice_Rec_336345 Human_miRNA_ID_1542118,Human_miRNA_ID_1595471 RMVar_hsa_circ_111421,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_114363,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_100141,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_268283,RMVar_hsa_circ_92305,RMVar_hsa_circ_205216,RMVar_hsa_circ_205219,RMVar_hsa_circ_88349,RMVar_hsa_circ_360666,RMVar_hsa_circ_205223,RMVar_hsa_circ_88829,RMVar_hsa_circ_205227,RMVar_hsa_circ_373125,RMVar_hsa_circ_205232,RMVar_hsa_circ_32396,RMVar_hsa_circ_35268,RMVar_hsa_circ_109126,RMVar_hsa_circ_205237,RMVar_hsa_circ_107947,RMVar_hsa_circ_205239,RMVar_hsa_circ_205240,RMVar_hsa_circ_124579,RMVar_hsa_circ_205241,RMVar_hsa_circ_127071,RMVar_hsa_circ_358368 114460 RMVar_ID_114460 Human_SNP_ID_839430643 m1A Human chr2 + 199792590 199792590 199792590 ATACATGCCTACCAACTACCCACTCACACATCACTTATTTCCCATTCTGTGCTCTTGCCCATGTT ATACATGCCTACCAACTACCCACTCACACATCCCTTATTTCCCATTCTGTGCTCTTGCCCATGTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:199792543..199792717 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 114461 RMVar_ID_114461 Human_SNP_ID_839436035 m1A Human chr2 - 191882158 191882158 191882158 TACCAGACGCTGGGCCTGGCCCGCGGCGCGTCAGACGAGGAGATCAAGCGGGCCTACCGCCGCCA TACCAGACGCTGGGCCTGGCCCGCGGCGCGTCGGACGAGGAGATCAAGCGGGCCTACCGCCGCCA T C DNAJB1P1 Ensembl:ENSG00000213946 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:191882108..191882200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 114462 RMVar_ID_114462 Human_SNP_ID_839443842 m1A Human chr2 - 232847513 232847513 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCGGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs114013774 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 12 head and neck 114463 RMVar_ID_114463 Human_SNP_ID_839443843 m1A Human chr2 - 232847513 232847513 232847513 GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCAGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC GCTGTGGCGGCTGCTGCTGCTGCTGCTGTGGCTGCTGCTGCTGCTGACGCTGCTGGTTGGCTTTC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:232847462..232850302 32194978 MeRIP-seq:(Medium) rs114013774 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 6 brain 114464 RMVar_ID_114464 Human_SNP_ID_839450265 m1A Human chr2 + 101006009 101006009 101006009 CCGTGTGCGGCTGTCCAGAAAACGTAATGAGGATGAAGATTCACCAAATAAGCTATATACTTTGG CCGTGTGCGGCTGTCCAGAAAACGTAATGAGGGTGAAGATTCACCAAATAAGCTATATACTTTGG A G RPL31 Ensembl:ENSG00000071082 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:101005912..101006026 26863196 MeRIP-seq:(Medium) rs1065720 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_530699,Human_RBP_ID_1576269,Human_RBP_ID_1894468,Human_RBP_ID_3590475,Human_RBP_ID_8497707,Human_RBP_ID_9091741,Human_RBP_ID_13559441,Human_RBP_ID_23815166,Human_RBP_ID_26998485 Human_Splice_Rec_281400,Human_Splice_Rec_281401,Human_Splice_Rec_281408,Human_Splice_Rec_281409,Human_Splice_Rec_281416,Human_Splice_Rec_281420,Human_Splice_Rec_281421,Human_Splice_Rec_281428,Human_Splice_Rec_281429,Human_Splice_Rec_281436,Human_Splice_Rec_281437,Human_Splice_Rec_281444,Human_Splice_Rec_281448,Human_Splice_Rec_281454,Human_Splice_Rec_281455 RMVar_hsa_circ_63143,RMVar_hsa_circ_114633,RMVar_hsa_circ_202205,RMVar_hsa_circ_202208,RMVar_hsa_circ_118770,RMVar_hsa_circ_202206,RMVar_hsa_circ_98723,RMVar_hsa_circ_121270,RMVar_hsa_circ_89706,RMVar_hsa_circ_202209,RMVar_hsa_circ_202207 114465 RMVar_ID_114465 Human_SNP_ID_839483816 m1A Human chr2 + 197488965 197488965 197488965 AATACTACAGAAGCAAAATCATTCTTGGACTCAGAACCCAAGAAACTTATTCATAATAATGAATG AATACTACAGAAGCAAAATCATTCTTGGACTCTGAACCCAAGAAACTTATTCATAATAATGAATG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:197488963..197489175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114466 RMVar_ID_114466 Human_SNP_ID_839492327 m1A Human chr2 + 26764359 26764359 26764359 AGCGAACCCCAGCGTCCGCCGACATGGCCTGGACCAAGTACCAGCTGTTCCTGGCCGGGCTCATG AGCGAACCCCAGCGTCCGCCGACATGGCCTGGGCCAAGTACCAGCTGTTCCTGGCCGGGCTCATG A G CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding exon,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:26764308..26764386 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4622283,Human_RBP_ID_20437597 Human_Splice_Rec_226369,Human_Splice_Rec_226377,Human_Splice_Rec_226387,Human_Splice_Rec_226391,Human_Splice_Rec_226399 114467 RMVar_ID_114467 Human_SNP_ID_839535838 m1A Human chr2 + 148645038 148645038 148645038 GGCGGGGAGACAATGAGTAAACTCTCCTTCCGAGCGCGGGCGCTGGACGCCGCCAAGCCGCTGCC GGCGGGGAGACAATGAGTAAACTCTCCTTCCGTGCGCGGGCGCTGGACGCCGCCAAGCCGCTGCC A T EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:148644995..148645131 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_535294,Human_RBP_ID_4624781,Human_RBP_ID_6834059,Human_RBP_ID_13633855,Human_RBP_ID_18747274,Human_RBP_ID_22996881,Human_RBP_ID_26770395 RMVar_hsa_circ_203733,RMVar_hsa_circ_83945,RMVar_hsa_circ_127128,RMVar_hsa_circ_203734 114468 RMVar_ID_114468 Human_SNP_ID_839546303 m1A Human chr2 + 231712479 231712477 231712479 GGAAGAGGATGGAGATGAAGATGAGGAAGCTGAGTCAGCTACGGGCAAGCGGGCAGCTGAAGATG GGAAGAGGATGGAGATGAAGATGAGGAAGCT__GTCAGCTACGGGCAAGCGGGCAGCTGAAGATG TGA T PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:231712376..231712568 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - Human_RBP_ID_60394,Human_RBP_ID_242138,Human_RBP_ID_545770,Human_RBP_ID_828843,Human_RBP_ID_920683,Human_RBP_ID_1068046,Human_RBP_ID_1584273,Human_RBP_ID_1912575,Human_RBP_ID_3618043,Human_RBP_ID_3959922,Human_RBP_ID_5651995,Human_RBP_ID_6895188,Human_RBP_ID_8513856,Human_RBP_ID_9385683,Human_RBP_ID_13794986,Human_RBP_ID_18166955,Human_RBP_ID_18412835,Human_RBP_ID_21982440,Human_RBP_ID_22996929,Human_RBP_ID_23115088,Human_RBP_ID_23856733,Human_RBP_ID_24545979,Human_RBP_ID_26338861,Human_RBP_ID_27007850,Human_RBP_ID_27818082 Human_Splice_Rec_370020,Human_Splice_Rec_370021,Human_Splice_Rec_370028,Human_Splice_Rec_370029,Human_Splice_Rec_370038,Human_Splice_Rec_370039,Human_Splice_Rec_370046,Human_Splice_Rec_370047,Human_Splice_Rec_370054,Human_Splice_Rec_370055,Human_Splice_Rec_370062,Human_Splice_Rec_370066,Human_Splice_Rec_370067,Human_Splice_Rec_370074,Human_Splice_Rec_370075,Human_Splice_Rec_370080,Human_Splice_Rec_370081,Human_Splice_Rec_370088,Human_Splice_Rec_370089 Human_miRNA_ID_1006942,Human_miRNA_ID_2453407,Human_miRNA_ID_2453408 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600,RMVar_hsa_circ_371274,RMVar_hsa_circ_207602 114469 RMVar_ID_114469 Human_SNP_ID_839601989 m1A Human chr2 - 26278676 26278676 26278676 CATTTTCCTTGAGTGACGAATAGGGACATCGGACATCAACTCAACACCACCTGCCACGATCACAT CATTTTCCTTGAGTGACGAATAGGGACATCGGGCATCAACTCAACACCACCTGCCACGATCACAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:26261582..26280077 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 10 caecum,large intestine 114470 RMVar_ID_114470 Human_SNP_ID_839626723 m1A Human chr2 - 201079004 201079004 201079004 TTAATTCATCTTACCGGCCCCATGGATCCCTTAGCCCTTTTGCAGCCAGCTTCTTCTGGATAGTT TTAATTCATCTTACCGGCCCCATGGATCCCTTGGCCCTTTTGCAGCCAGCTTCTTCTGGATAGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:201078910..201079068 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 SKCM,large_intestine adenocarcinoma 4 large intestine 114471 RMVar_ID_114471 Human_SNP_ID_839719581 m1A Human chr2 - 235716397 235716397 235716397 CTACCAGGAAACTGCCCACTAGGTCACCCGCAACTTCCATTTCAAAGCCACTAGCCTGTCTCGCT CTACCAGGAAACTGCCCACTAGGTCACCCGCAGCTTCCATTTCAAAGCCACTAGCCTGTCTCGCT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:235716391..235716475 26863196 MeRIP-seq:(Medium) rs1159859401 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114472 RMVar_ID_114472 Human_SNP_ID_839729449 m1A Human chr2 - 119367036 119367036 119367036 CGCTGTACCTGAGACATCCTGGCCGACTTGCAAGAACTCCAGGGAGACAGCGGAGGAGGCGAGGA CGCTGTACCTGAGACATCCTGGCCGACTTGCAGGAACTCCAGGGAGACAGCGGAGGAGGCGAGGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:119366969..119367131;chr2:119366969..119367129;chr2:119366976..119367131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine 114473 RMVar_ID_114473 Human_SNP_ID_839733392 m1A Human chr2 + 26979724 26979724 26979724 AGGTACAGCATCAGCAAAGGAATGGCCGTGGGAAGGGGTGTGGTGGGGTTTGTAGGCAGGGCAGC AGGTACAGCATCAGCAAAGGAATGGCCGTGGGCAGGGGTGTGGTGGGGTTTGTAGGCAGGGCAGC A C MAPRE3 Ensembl:ENSG00000084764 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:26979720..26979886 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 114474 RMVar_ID_114474 Human_SNP_ID_839734121 m1A Human chr2 - 134306964 134306964 134306964 TGCCTCCTCATTAGGAAGAGGCCTGCTCCTGGAACTGACACTGAAATGTATCAGCAGAGAGTAGC TGCCTCCTCATTAGGAAGAGGCCTGCTCCTGGGACTGACACTGAAATGTATCAGCAGAGAGTAGC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:134306883..134307010 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast 114475 RMVar_ID_114475 Human_SNP_ID_839752082 m1A Human chr2 - 98822884 98822884 98822884 CCCCCAGGGCCGGCGCCTGAGCCCGAGAGAGAAGCGGAGACGGAGCCCGAGAGAGGAGCGGGGAC CCCCCAGGGCCGGCGCCTGAGCCCGAGAGAGAGGCGGAGACGGAGCCCGAGAGAGGAGCGGGGAC T C KIAA1211L Ensembl:ENSG00000196872 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:98822742..98823026 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - RMVar_hsa_circ_268330 114476 RMVar_ID_114476 Human_SNP_ID_839758738 m1A Human chr2 + 113596805 113596805 113596805 CCCCTGTAGGCCAAGGCGCCAGGCAGGACGACAGCAGCAGCAGCGCGTCTCCTTCAGGTGGGAGC CCCCTGTAGGCCAAGGCGCCAGGCAGGACGACGGCAGCAGCAGCGCGTCTCCTTCAGGTGGGAGC A G WASH2P Ensembl:ENSG00000146556 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1178326930 Functional Loss SNV TCGA,ICGC 33..33 33 SARC,LUSC,ESCA 3 - Human_RBP_ID_148242,Human_RBP_ID_919910 Human_Splice_Rec_290427,Human_Splice_Rec_290441 114477 RMVar_ID_114477 Human_SNP_ID_839759601 m1A Human chr2 - 241236673 241236673 241236673 AGATTGTGACCCCGGCTCTCCAAGGAGGTGTGACATCATCATCATCTCTGGCCGGAAAGAAAAGT AGATTGTGACCCCGGCTCTCCAAGGAGGTGTGTCATCATCATCATCTCTGGCCGGAAAGAAAAGT T A HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:241236651..241236675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 6 head and neck Human_RBP_ID_57667,Human_RBP_ID_546992,Human_RBP_ID_922566,Human_RBP_ID_1022571,Human_RBP_ID_1134691,Human_RBP_ID_1913679,Human_RBP_ID_6900743,Human_RBP_ID_8846972,Human_RBP_ID_9295700,Human_RBP_ID_9385844,Human_RBP_ID_17390730,Human_RBP_ID_17965805,Human_RBP_ID_18180370,Human_RBP_ID_18193438,Human_RBP_ID_22990916,Human_RBP_ID_26340513,Human_RBP_ID_27009049,Human_RBP_ID_27478801 Human_Splice_Rec_381296,Human_Splice_Rec_381297,Human_Splice_Rec_381350,Human_Splice_Rec_381351,Human_Splice_Rec_381404,Human_Splice_Rec_381405,Human_Splice_Rec_381458,Human_Splice_Rec_381459,Human_Splice_Rec_381490,Human_Splice_Rec_381491,Human_Splice_Rec_381528,Human_Splice_Rec_381529,Human_Splice_Rec_381553,Human_Splice_Rec_381568,Human_Splice_Rec_381569 Human_miRNA_ID_2064505,Human_miRNA_ID_2702380,Human_miRNA_ID_2933685 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_27144,RMVar_hsa_circ_107101,RMVar_hsa_circ_323740,RMVar_hsa_circ_208054,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_113256,RMVar_hsa_circ_35176,RMVar_hsa_circ_208057,RMVar_hsa_circ_208058,RMVar_hsa_circ_208056,RMVar_hsa_circ_208062,RMVar_hsa_circ_87225,RMVar_hsa_circ_114474,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_208061,RMVar_hsa_circ_89030,RMVar_hsa_circ_30135,RMVar_hsa_circ_336624,RMVar_hsa_circ_352648,RMVar_hsa_circ_79638,RMVar_hsa_circ_39483,RMVar_hsa_circ_60705,RMVar_hsa_circ_54737,RMVar_hsa_circ_113630,RMVar_hsa_circ_208067,RMVar_hsa_circ_208068,RMVar_hsa_circ_208066,RMVar_hsa_circ_114625,RMVar_hsa_circ_57770,RMVar_hsa_circ_78553,RMVar_hsa_circ_55360,RMVar_hsa_circ_92839,RMVar_hsa_circ_118015,RMVar_hsa_circ_208071,RMVar_hsa_circ_208072,RMVar_hsa_circ_208070,RMVar_hsa_circ_208075,RMVar_hsa_circ_82300,RMVar_hsa_circ_89716,RMVar_hsa_circ_208077,RMVar_hsa_circ_208078,RMVar_hsa_circ_208076,RMVar_hsa_circ_208074,RMVar_hsa_circ_63741,RMVar_hsa_circ_57322 114478 RMVar_ID_114478 Human_SNP_ID_839760996 m1A Human chr2 - 188997176 188997176 188997176 GGTCCTCCAGGGCCACCTCGTTCTCCATTCTTACCAGGAGCACCCTAAAGAAGAAGTGGTCGGTA GGTCCTCCAGGGCCACCTCGTTCTCCATTCTTTCCAGGAGCACCCTAAAGAAGAAGTGGTCGGTA T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:188997151..188997175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 2 skin,head and neck 114479 RMVar_ID_114479 Human_SNP_ID_839778168 m1A Human chr2 - 11287726 11287726 11287726 TCCTCTTTTTATTTCTTAACAGGATGGCTTAAATTCCTTGGTCCTTGATTTAGATTTTCCTGCTT TCCTCTTTTTATTTCTTAACAGGATGGCTTAATTTCCTTGGTCCTTGATTTAGATTTTCCTGCTT T A ROCK2 Ensembl:ENSG00000134318 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:11287676..11287750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_Splice_Rec_218226,Human_Splice_Rec_218227,Human_Splice_Rec_218290,Human_Splice_Rec_218291,Human_Splice_Rec_218414,Human_Splice_Rec_218415,Human_Splice_Rec_218445,Human_Splice_Rec_218458,Human_Splice_Rec_218459 RMVar_hsa_circ_113994,RMVar_hsa_circ_197006,RMVar_hsa_circ_94695,RMVar_hsa_circ_197031,RMVar_hsa_circ_6528,RMVar_hsa_circ_111154,RMVar_hsa_circ_197045,RMVar_hsa_circ_197046,RMVar_hsa_circ_357373,RMVar_hsa_circ_311577,RMVar_hsa_circ_197047,RMVar_hsa_circ_197048 114480 RMVar_ID_114480 Human_SNP_ID_839780659 m1A Human chr2 + 740684 740684 740684 GGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCAGCGAGGATCTTCCCTCAGAGCCTGGCGAGGGG GGGCGTGGCCCAGCCAGGAGAGCTGGAGAGGCCGCGAGGATCTTCCCTCAGAGCCTGGCGAGGGG A C lnc-SNTG2-8 RNACentral:URS00008B6BBC lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:740597..740925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114481 RMVar_ID_114481 Human_SNP_ID_839825803 m1A Human chr2 - 183607609 183607609 183607609 ACAAGGTGGGATTACCTGACCCAGGTTGAAAAAGAGTGCAAAGAAAAAGAGAAGCCCTCCTATGA ACAAGGTGGGATTACCTGACCCAGGTTGAAAAGGAGTGCAAAGAAAAAGAGAAGCCCTCCTATGA T C CACYBPP2 Ensembl:ENSG00000177855 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878959244 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114482 RMVar_ID_114482 Human_SNP_ID_839853325 m1A Human chr2 + 130182774 130182774 130182774 TCTCTGCCCACGTCGAGCGTGCCCGAGACCCGAGGTCAGAGCTGGGCCCGCTGTCCCTGCCCCAG TCTCTGCCCACGTCGAGCGTGCCCGAGACCCGTGGTCAGAGCTGGGCCCGCTGTCCCTGCCCCAG A T MZT2B Ensembl:ENSG00000152082 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr2:130182719..130182818;chr2:130182726..130182800 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_17658169,Human_RBP_ID_18193387,Human_RBP_ID_24553025 Human_Splice_Rec_296999,Human_Splice_Rec_297003,Human_Splice_Rec_297007,Human_Splice_Rec_297011,Human_Splice_Rec_297017,Human_Splice_Rec_297023,Human_Splice_Rec_297025 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 114483 RMVar_ID_114483 Human_SNP_ID_839861476 m1A Human chr2 - 241751998 241751998 241751998 GGTCCCGGTAACAGTGACCAATGGCTCCCACTATCCAGGCCCCGGTGACGGTGACCGAGGGCTCC GGTCCCGGTAACAGTGACCAATGGCTCCCACTGTCCAGGCCCCGGTGACGGTGACCGAGGGCTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:241751671..241752224 26863196 MeRIP-seq:(Medium) rs4992235 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 4 brain 114484 RMVar_ID_114484 Human_SNP_ID_839871411 m1A Human chr2 - 24076281 24076281 24076281 ATCTAACGCGGTGTAACCCCCGAAGCCGAGCGAGCTCCGGAGGAATTTCAGTATCTGCTACGGTA ATCTAACGCGGTGTAACCCCCGAAGCCGAGCGGGCTCCGGAGGAATTTCAGTATCTGCTACGGTA T C SF3B6 Ensembl:ENSG00000115128 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1201166407 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_547548,Human_RBP_ID_775016,Human_RBP_ID_1585271,Human_RBP_ID_1914190,Human_RBP_ID_4623148,Human_RBP_ID_5444707,Human_RBP_ID_5470650,Human_RBP_ID_18421710,Human_RBP_ID_22451125,Human_RBP_ID_22815237,Human_RBP_ID_23863106 Human_Splice_Rec_222571,Human_Splice_Rec_222577 RMVar_hsa_circ_92701,RMVar_hsa_circ_197560 114485 RMVar_ID_114485 Human_SNP_ID_839889892 m1A Human chr2 - 38751309 38751309 38751309 GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC GGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCTCTCGAGCCCTGGGCGCTGCTTGCTAAAGAGCC T A SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr2:38751067..38751375;chr2:38751210..38751350;chr2:38751051..38751375 26863196 MeRIP-seq:(Medium) rs117377682 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_58102,Human_RBP_ID_550758,Human_RBP_ID_1196050,Human_RBP_ID_1301047,Human_RBP_ID_1586765,Human_RBP_ID_4609060,Human_RBP_ID_6918317,Human_RBP_ID_8518694,Human_RBP_ID_8848191,Human_RBP_ID_9106189,Human_RBP_ID_9330424,Human_RBP_ID_9383530,Human_RBP_ID_13881226,Human_RBP_ID_18421744,Human_RBP_ID_22076218,Human_RBP_ID_22452151,Human_RBP_ID_22992642,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27840017 Human_Splice_Rec_237339,Human_Splice_Rec_237353,Human_Splice_Rec_237365,Human_Splice_Rec_237381,Human_Splice_Rec_237415,Human_Splice_Rec_237433,Human_Splice_Rec_237445 Human_miRNA_ID_2756038 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 114486 RMVar_ID_114486 Human_SNP_ID_839889893 m1A Human chr2 - 99489869 99489869 99489869 GGGCACTGGCGGCGGCGGGGCCGGGGTCCGCAAGGCCGGAGAAGGCCGCCGGGCCCGGGCATGGT GGGCACTGGCGGCGGCGGGGCCGGGGTCCGCACGGCCGGAGAAGGCCGCCGGGCCCGGGCATGGT T G REV1 Ensembl:ENSG00000135945 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:99489777..99489959 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4575348,Human_RBP_ID_18422291,Human_RBP_ID_18493519 Human_Splice_Rec_280399,Human_Splice_Rec_280443,Human_Splice_Rec_280487 114487 RMVar_ID_114487 Human_SNP_ID_839914502 m1A Human chr2 + 210656528 210656528 210656528 TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTATCTCTCATGCCATCTCTGAACATGTTGAAGAT TAAAATCCTTTTTTTTTTTTTTTGGCCAGGTTTTCTCTCATGCCATCTCTGAACATGTTGAAGAT A T CPS1 Ensembl:ENSG00000021826 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210656526..210656654 26863196 MeRIP-seq:(Medium) rs779559626 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 21 head and neck Human_RBP_ID_56002,Human_RBP_ID_2620884,Human_RBP_ID_8511123 Human_Splice_Rec_353140,Human_Splice_Rec_353218,Human_Splice_Rec_353294,Human_Splice_Rec_353370,Human_Splice_Rec_353444,Human_Splice_Rec_353526,Human_Splice_Rec_353580,Human_Splice_Rec_353630 RMVar_hsa_circ_297846,RMVar_hsa_circ_302722,RMVar_hsa_circ_35167,RMVar_hsa_circ_67863,RMVar_hsa_circ_6014,RMVar_hsa_circ_56320,RMVar_hsa_circ_352319,RMVar_hsa_circ_352584,RMVar_hsa_circ_358533,RMVar_hsa_circ_369098,RMVar_hsa_circ_206575,RMVar_hsa_circ_360750,RMVar_hsa_circ_356458,RMVar_hsa_circ_103202,RMVar_hsa_circ_360360,RMVar_hsa_circ_368273,RMVar_hsa_circ_355151,RMVar_hsa_circ_353791,RMVar_hsa_circ_55792,RMVar_hsa_circ_56784,RMVar_hsa_circ_69366,RMVar_hsa_circ_206577,RMVar_hsa_circ_55863,RMVar_hsa_circ_6227,RMVar_hsa_circ_56999,RMVar_hsa_circ_57477 114488 RMVar_ID_114488 Human_SNP_ID_839926723 m1A Human chr2 - 265001 265001 265001 ACATGAGTAAGTCGGCGCCCTCTTACCCAGACACACAAACAGCACGGACTTGGTAGCCTGTTCCG ACATGAGTAAGTCGGCGCCCTCTTACCCAGACCCACAAACAGCACGGACTTGGTAGCCTGTTCCG T G SH3YL1 Ensembl:ENSG00000035115 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr2:264951..265069;chr2:264951..265070 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114489 RMVar_ID_114489 Human_SNP_ID_839970482 m1A Human chr2 - 231464436 231464436 231464436 TGGCCTTCGGGTGTACGTGCTCCGGGATCTTCAGCACCCGCGGCCGCCATCGCCGTCGCTTGGCT TGGCCTTCGGGTGTACGTGCTCCGGGATCTTCGGCACCCGCGGCCGCCATCGCCGTCGCTTGGCT T C NCL Ensembl:ENSG00000115053 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr2:231464230..231464500;chr2:231464239..231464500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_242114,Human_RBP_ID_1022285,Human_RBP_ID_1195063,Human_RBP_ID_1299880,Human_RBP_ID_1584259,Human_RBP_ID_1912565,Human_RBP_ID_3618030,Human_RBP_ID_4623905,Human_RBP_ID_5262771,Human_RBP_ID_5444592,Human_RBP_ID_5501799,Human_RBP_ID_6895145,Human_RBP_ID_8257499,Human_RBP_ID_8513836,Human_RBP_ID_8846364,Human_RBP_ID_9385672,Human_RBP_ID_13794899,Human_RBP_ID_17275397,Human_RBP_ID_17506492,Human_RBP_ID_17952210,Human_RBP_ID_18755802,Human_RBP_ID_22076890,Human_RBP_ID_22505229,Human_RBP_ID_22815011,Human_RBP_ID_23856693,Human_RBP_ID_24545972,Human_RBP_ID_27007818,Human_RBP_ID_27287489,Human_RBP_ID_27478285,Human_RBP_ID_27819402 RMVar_hsa_circ_89925,RMVar_hsa_circ_207583,RMVar_hsa_circ_87001,RMVar_hsa_circ_207587,RMVar_hsa_circ_207594,RMVar_hsa_circ_98924 114490 RMVar_ID_114490 Human_SNP_ID_839994170 m1A Human chr2 + 117830679 117830678 117830680 ACCAAGAAAGTTGAGAAATCCAAAATCTTTAAACACATTAGCAAGAAATCATCTGACAGCAGGCA ACCAAGAAAGTTGAGAAATCCAAAATCTTTAA__ACATTAGCAAGAAATCATCTGACAGCAGGCA AAC A DDX18 Ensembl:ENSG00000088205 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:117830589..117830839 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 KIRC 1 - Human_RBP_ID_1896405,Human_RBP_ID_3593070,Human_RBP_ID_8257240,Human_RBP_ID_13588276,Human_RBP_ID_17273342,Human_RBP_ID_17938554,Human_RBP_ID_20451519,Human_RBP_ID_24485890 Human_Splice_Rec_291280,Human_Splice_Rec_291316 RMVar_hsa_circ_107155,RMVar_hsa_circ_202793,RMVar_hsa_circ_96522,RMVar_hsa_circ_76033,RMVar_hsa_circ_202794,RMVar_hsa_circ_202796,RMVar_hsa_circ_110900,RMVar_hsa_circ_202800,RMVar_hsa_circ_125012,RMVar_hsa_circ_202802 114491 RMVar_ID_114491 Human_SNP_ID_839994188 m1A Human chr2 + 27104377 27104377 27104377 CTGTCATCGTCAAAGGTAACATCCTTCCTGGAACTGGAACAAGGAAGAGAATCAGGGGTCGGGGG CTGTCATCGTCAAAGGTAACATCCTTCCTGGAGCTGGAACAAGGAAGAGAATCAGGGGTCGGGGG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:27104346..27104435 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 114492 RMVar_ID_114492 Human_SNP_ID_839999058 m1A Human chr2 - 176122802 176122802 176122802 CACGTAGTAGTTGCTGAGGGTGCCACTGGAAGACATTTTGAGGCGTCCCGCACTCCCACCCAACA CACGTAGTAGTTGCTGAGGGTGCCACTGGAAGTCATTTTGAGGCGTCCCGCACTCCCACCCAACA T A HOXD-AS2 Ensembl:ENSG00000237380 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:176122752..176123056 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 114493 RMVar_ID_114493 Human_SNP_ID_840005866 m1A Human chr2 + 169733925 169733925 169733925 CGTGCGGGGGGCTGTTCGGGTGGAGGCGGGGGAGCCGCCGGGACACCAAAATAGGAGCTGCTTGT CGTGCGGGGGGCTGTTCGGGTGGAGGCGGGGGGGCCGCCGGGACACCAAAATAGGAGCTGCTTGT A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:169733878..169734062 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_774378,Human_RBP_ID_829149,Human_RBP_ID_4585871,Human_RBP_ID_5239678,Human_RBP_ID_5322658,Human_RBP_ID_8852126,Human_RBP_ID_9296842,Human_RBP_ID_17943442,Human_RBP_ID_18422395 RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 114494 RMVar_ID_114494 Human_SNP_ID_840010742 m1A Human chr2 - 96816309 96816309 96816309 TGCCCAGGCAGAGCGCGGCGAACAACCAGCCTAACCGACCCGCCGCAGCTACCGCCGCCGCCATC TGCCCAGGCAGAGCGCGGCGAACAACCAGCCTTACCGACCCGCCGCAGCTACCGCCGCCGCCATC T A CNNM3-DT RNACentral:URS00008BB4F7 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:96816251..96817236 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 114495 RMVar_ID_114495 Human_SNP_ID_840013057 m1A Human chr2 + 176122763 176122763 176122763 GGGCGCCGGCGGGGAGCTGCTCGGCGGCGGACAGTGTAATGTTGGGTGGGAGTGCGGGACGCCTC GGGCGCCGGCGGGGAGCTGCTCGGCGGCGGACGGTGTAATGTTGGGTGGGAGTGCGGGACGCCTC A G HOXD9 Ensembl:ENSG00000128709 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:176122713..176122878 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_243621,Human_RBP_ID_1193938,Human_RBP_ID_6855387,Human_RBP_ID_13692917 114496 RMVar_ID_114496 Human_SNP_ID_840018609 m1A Human chr2 + 231712879 231712876 231712879 ACTAGACAGCAAAAAAGGAAAAGTTAAACTAAAAAAAAAAAGGCCGCCGTGACCTATTCACCCTC ACTAGACAGCAAAAAAGGAAAAGTTAAACT___AAAAAAAAGGCCGCCGTGACCTATTCACCCTC TAAA T PTMA Ensembl:ENSG00000187514 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:231712763..231713025 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 COAD 3 - Human_RBP_ID_60396,Human_RBP_ID_545773,Human_RBP_ID_1022291,Human_RBP_ID_1068047,Human_RBP_ID_1912578,Human_RBP_ID_2627110,Human_RBP_ID_3618044,Human_RBP_ID_4630962,Human_RBP_ID_6895196,Human_RBP_ID_8513858,Human_RBP_ID_9385686,Human_RBP_ID_13794993,Human_RBP_ID_17275399,Human_RBP_ID_17390565,Human_RBP_ID_17506497,Human_RBP_ID_17952236,Human_RBP_ID_18755825,Human_RBP_ID_22248660,Human_RBP_ID_22452665,Human_RBP_ID_23856735,Human_RBP_ID_26338864,Human_RBP_ID_26488273,Human_RBP_ID_27007855,Human_RBP_ID_27287516,Human_RBP_ID_27478293 Human_Splice_Rec_370022,Human_Splice_Rec_370030,Human_Splice_Rec_370040,Human_Splice_Rec_370048,Human_Splice_Rec_370056,Human_Splice_Rec_370068,Human_Splice_Rec_370076,Human_Splice_Rec_370082,Human_Splice_Rec_370090 RMVar_hsa_circ_96802,RMVar_hsa_circ_207599,RMVar_hsa_circ_97805,RMVar_hsa_circ_207600 114497 RMVar_ID_114497 Human_SNP_ID_840029319 m1A Human chr2 - 96144884 96144884 96144884 TTCCCTGCTGATCGTGCTCTTCCCCTCCTTGCAGGAGGCTTCGACGGCTTCCAGGGCTGCTGTCC TTCCCTGCTGATCGTGCTCTTCCCCTCCTTGCTGGAGGCTTCGACGGCTTCCAGGGCTGCTGTCC T A DUSP2 Ensembl:ENSG00000158050 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96144860..96145242 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114498 RMVar_ID_114498 Human_SNP_ID_840082470 m1A Human chr2 - 96143851 96143851 96143851 CCCCAACTTCAGTTTCATGGGGCAGCTGCTGCAGTTTGAGACCCAGGTGCTGTGTCACTGAGGTG CCCCAACTTCAGTTTCATGGGGCAGCTGCTGCTGTTTGAGACCCAGGTGCTGTGTCACTGAGGTG T A DUSP2 Ensembl:ENSG00000158050 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr2:96143801..96144025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 1 haematopoietic and lymphoid tissue Human_miRNA_ID_2516262 RMVar_hsa_circ_94669,RMVar_hsa_circ_201829 114499 RMVar_ID_114499 Human_SNP_ID_840108850 m1A Human chr2 - 96253911 96253911 96253911 CCTCCTGCGCCACTACCCCACAGAGGAAGAGGAGCAGGCGCTGGAGCTGCTCTCAGAGATGGAAG CCTCCTGCGCCACTACCCCACAGAGGAAGAGGGGCAGGCGCTGGAGCTGCTCTCAGAGATGGAAG T C TMEM127 Ensembl:ENSG00000135956 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:96253787..96253987 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_778188,Human_RBP_ID_22765926 Human_miRNA_ID_654053 114500 RMVar_ID_114500 Human_SNP_ID_840118389 m1A Human chr2 - 45555 45555 45555 GACGACGAGGGGCTGCAGGAGGAGGAGCTGATAGAGCAGGTGCCCAGCACCACTTCGGTCATCGA GACGACGAGGGGCTGCAGGAGGAGGAGCTGATGGAGCAGGTGCCCAGCACCACTTCGGTCATCGA T C FAM110C Ensembl:ENSG00000184731 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:45506..46052 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 114501 RMVar_ID_114501 Human_SNP_ID_840142650 m1A Human chr2 - 32357254 32357254 32357254 GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCAGCCGCCATCTTCCGGCCTGCGCTCAGCACAAT GAGCAGCCGGGGCCCGAGGCCGCCGCAGCCGCTGCCGCCATCTTCCGGCCTGCGCTCAGCACAAT T A lnc-NLRC4-4-002 RNACentral:URS00008C1097 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:32357205..32357359 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_198328 114502 RMVar_ID_114502 Human_SNP_ID_840154416 m1A Human chr2 - 71184996 71184996 71184996 GCCCAGGCTCCTGAACCATCAGGAACCCAGGAATCTACCCAACTGTGAGGAGGGGGCAGGCCTTC GCCCAGGCTCCTGAACCATCAGGAACCCAGGAGTCTACCCAACTGTGAGGAGGGGGCAGGCCTTC T C PAIP2B Ensembl:ENSG00000124374 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs187181 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_18318812 114503 RMVar_ID_114503 Human_SNP_ID_840157507 m1A Human chr2 + 201272660 201272660 201272660 CTCCTCTTAGAACCTGCTGGATATTTTCATAGAGATGGAGAAGAGGGTCATCCTGGGAGAAGGAA CTCCTCTTAGAACCTGCTGGATATTTTCATAGGGATGGAGAAGAGGGTCATCCTGGGAGAAGGAA A G CASP8 Ensembl:ENSG00000064012 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:201271594..201272761 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_919114,Human_RBP_ID_6873241,Human_RBP_ID_26340229 Human_Splice_Rec_345534,Human_Splice_Rec_345550,Human_Splice_Rec_345562,Human_Splice_Rec_345584,Human_Splice_Rec_345600,Human_Splice_Rec_345606,Human_Splice_Rec_345624,Human_Splice_Rec_345636,Human_Splice_Rec_345644,Human_Splice_Rec_345660,Human_Splice_Rec_345670,Human_Splice_Rec_345676,Human_Splice_Rec_345682,Human_Splice_Rec_345688,Human_Splice_Rec_345704,Human_Splice_Rec_345718 RMVar_hsa_circ_63172,RMVar_hsa_circ_355814,RMVar_hsa_circ_205887,RMVar_hsa_circ_371583 114504 RMVar_ID_114504 Human_SNP_ID_840207459 m1A Human chr2 + 27033050 27033050 27033050 GGCGACCAAGACGGCGGGCGTGGGGCGGTGGGAGGTAGTGAAGAAGGGTCGGCGGCCTGGGGTCG GGCGACCAAGACGGCGGGCGTGGGGCGGTGGGGGGTAGTGAAGAAGGGTCGGCGGCCTGGGGTCG A G TMEM214 Ensembl:ENSG00000119777 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:27032999..27033157 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_58357,Human_RBP_ID_775455,Human_RBP_ID_828571,Human_RBP_ID_1067888,Human_RBP_ID_3637895,Human_RBP_ID_3957656,Human_RBP_ID_4622287,Human_RBP_ID_5146519,Human_RBP_ID_5379158,Human_RBP_ID_8851795,Human_RBP_ID_9347396,Human_RBP_ID_9428603,Human_RBP_ID_17392579,Human_RBP_ID_17658002,Human_RBP_ID_18421721,Human_RBP_ID_18947678,Human_RBP_ID_19001283,Human_RBP_ID_22533567,Human_RBP_ID_22597770,Human_RBP_ID_26339094 Human_miRNA_ID_2867089 RMVar_hsa_circ_123128,RMVar_hsa_circ_197839 114505 RMVar_ID_114505 Human_SNP_ID_840214276 m1A Human chr2 + 27057416 27057416 27057416 CCCCCCTCCCCCGCCGGCTTTCCCCTCCAGATACACTGTGGAACTATTTGAGCAGGTATGAATAC CCCCCCTCCCCCGCCGGCTTTCCCCTCCAGATGCACTGTGGAACTATTTGAGCAGGTATGAATAC A G AGBL5 Ensembl:ENSG00000084693 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:27057309..27059257 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_5118742 Human_Splice_Rec_226847,Human_Splice_Rec_226895,Human_Splice_Rec_226923 RMVar_hsa_circ_24376,RMVar_hsa_circ_84980,RMVar_hsa_circ_197868,RMVar_hsa_circ_54257,RMVar_hsa_circ_128019,RMVar_hsa_circ_115316,RMVar_hsa_circ_94549,RMVar_hsa_circ_197869,RMVar_hsa_circ_197870,RMVar_hsa_circ_197872,RMVar_hsa_circ_197871,RMVar_hsa_circ_311723 114506 RMVar_ID_114506 Human_SNP_ID_840220476 m1A Human chr2 + 238238914 238238914 238238914 GCTGCGGGCACCAAGTCGGGCCCCTCAGCAGGAGCCTGACTCAGTTCAGCCTCAGGGGCCTCCTC GCTGCGGGCACCAAGTCGGGCCCCTCAGCAGGGGCCTGACTCAGTTCAGCCTCAGGGGCCTCCTC A G AC012485.1 Ensembl:ENSG00000225057 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr2:238238812..238239062 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 KICH,kidney chromophobe_renal_cell_carcinoma 7 kidney 114507 RMVar_ID_114507 Human_SNP_ID_840225884 m1A Human chr2 - 239134643 239134643 239134643 ACTGTGATGGTCATCGTGTGTTCTGTCCCCAGACGAGTTTGGCGCACAGACTTGTGGCACGAGAA ACTGTGATGGTCATCGTGTGTTCTGTCCCCAGGCGAGTTTGGCGCACAGACTTGTGGCACGAGAA T C HDAC4 Ensembl:ENSG00000068024 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:239134601..239134650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_2630687,Human_RBP_ID_5198074,Human_RBP_ID_22670520 Human_Splice_Rec_377226,Human_Splice_Rec_377278,Human_Splice_Rec_377354,Human_Splice_Rec_377392,Human_Splice_Rec_377422,Human_Splice_Rec_377444,Human_Splice_Rec_377452,Human_Splice_Rec_377460 RMVar_hsa_circ_111174,RMVar_hsa_circ_110110,RMVar_hsa_circ_207910,RMVar_hsa_circ_207909,RMVar_hsa_circ_89755,RMVar_hsa_circ_102606,RMVar_hsa_circ_86792,RMVar_hsa_circ_207914,RMVar_hsa_circ_207915,RMVar_hsa_circ_207916,RMVar_hsa_circ_99575,RMVar_hsa_circ_207917,RMVar_hsa_circ_26194,RMVar_hsa_circ_79524,RMVar_hsa_circ_74490,RMVar_hsa_circ_61582,RMVar_hsa_circ_108992,RMVar_hsa_circ_365766,RMVar_hsa_circ_207918,RMVar_hsa_circ_323302,RMVar_hsa_circ_207919,RMVar_hsa_circ_73213,RMVar_hsa_circ_363198,RMVar_hsa_circ_47531,RMVar_hsa_circ_3330,RMVar_hsa_circ_21847 114508 RMVar_ID_114508 Human_SNP_ID_840234792 m1A Human chr2 - 37147824 37147824 37147824 AGCATCACTCATTCAAATGTCTCTTCCATTGTAGGATACGGGAAGAAGAAATGGCTGGTGATCTT AGCATCACTCATTCAAATGTCTCTTCCATTGTGGGATACGGGAAGAAGAAATGGCTGGTGATCTT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:37147795..37147879 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_60710,Human_RBP_ID_8234302,Human_RBP_ID_18999292,Human_RBP_ID_25574686 RMVar_hsa_circ_48602,RMVar_hsa_circ_2442,RMVar_hsa_circ_32277,RMVar_hsa_circ_49371 114509 RMVar_ID_114509 Human_SNP_ID_840251934 m1A Human chr2 - 151828200 151828200 151828200 GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGAGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT GCCGGGGGAAGCCAGGCGGCCCGGGTGTCTGGGGGGGGGGGGTCCGCTGCCCGAGAATGGGAATT T C ARL5A,AC068547.1 Ensembl:ENSG00000162980,Ensembl:ENSG00000283228 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr2:151828151..151828350 32194978 MeRIP-seq:(Medium) rs201916854 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_535742,Human_RBP_ID_777294,Human_RBP_ID_4622717,Human_RBP_ID_9331192,Human_RBP_ID_17392807 Human_Splice_Rec_308451,Human_Splice_Rec_308479 114510 RMVar_ID_114510 Human_SNP_ID_840323248 m1A Human chr2 - 24068461 24068461 24068461 GTATATCTTAATTAAGTTTAACTTACCTCTCCAGGGGGAACACACCTGAAACTAGAGGAACAGCT GTATATCTTAATTAAGTTTAACTTACCTCTCCCGGGGGAACACACCTGAAACTAGAGGAACAGCT T G SF3B6 Ensembl:ENSG00000115128 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:24067683..24073691 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_917642,Human_RBP_ID_22074479 RMVar_hsa_circ_92701,RMVar_hsa_circ_197560,RMVar_hsa_circ_197561,RMVar_hsa_circ_298485 114511 RMVar_ID_114511 Human_SNP_ID_840333571 m1A Human chr2 - 61876194 61876194 61876194 TCAAATAGTGGTTTCTGACTATGCCCAGATGGACCGAGTGCTGCGAGAAGAGAGAGCCTATATTT TCAAATAGTGGTTTCTGACTATGCCCAGATGGGCCGAGTGCTGCGAGAAGAGAGAGCCTATATTT T C CCT4 Ensembl:ENSG00000115484 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:61876126..61876225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_775220,Human_RBP_ID_829891,Human_RBP_ID_1588691,Human_RBP_ID_1921336,Human_RBP_ID_3630609,Human_RBP_ID_4613179,Human_RBP_ID_6937512,Human_RBP_ID_8522735,Human_RBP_ID_8849316,Human_RBP_ID_9109470,Human_RBP_ID_13934382,Human_RBP_ID_17191976,Human_RBP_ID_17963973,Human_RBP_ID_18763579,Human_RBP_ID_22452219,Human_RBP_ID_22505794,Human_RBP_ID_23879279,Human_RBP_ID_27013532 Human_Splice_Rec_251840,Human_Splice_Rec_251841,Human_Splice_Rec_251864,Human_Splice_Rec_251865,Human_Splice_Rec_251878,Human_Splice_Rec_251879 RMVar_hsa_circ_200616,RMVar_hsa_circ_200606,RMVar_hsa_circ_108802,RMVar_hsa_circ_337085,RMVar_hsa_circ_200605,RMVar_hsa_circ_333000,RMVar_hsa_circ_37240,RMVar_hsa_circ_72743,RMVar_hsa_circ_200607,RMVar_hsa_circ_73668,RMVar_hsa_circ_200611,RMVar_hsa_circ_302031,RMVar_hsa_circ_332577,RMVar_hsa_circ_378013,RMVar_hsa_circ_312098,RMVar_hsa_circ_286599,RMVar_hsa_circ_288297,RMVar_hsa_circ_200609,RMVar_hsa_circ_200610,RMVar_hsa_circ_200608,RMVar_hsa_circ_264823,RMVar_hsa_circ_272525,RMVar_hsa_circ_279828,RMVar_hsa_circ_296004,RMVar_hsa_circ_273915,RMVar_hsa_circ_268222,RMVar_hsa_circ_269846,RMVar_hsa_circ_200617,RMVar_hsa_circ_200614,RMVar_hsa_circ_200615,RMVar_hsa_circ_200613,RMVar_hsa_circ_200620,RMVar_hsa_circ_284442,RMVar_hsa_circ_288317,RMVar_hsa_circ_346399,RMVar_hsa_circ_274755,RMVar_hsa_circ_200618,RMVar_hsa_circ_200619 114512 RMVar_ID_114512 Human_SNP_ID_840379250 m1A Human chr2 + 188996155 188996155 188996155 AGGGCATGCCCGGAAGTCCAGGAGGACCAGGAAGTGATGGGAAACCAGGGCCTCCCGTATGTACA AGGGCATGCCCGGAAGTCCAGGAGGACCAGGACGTGATGGGAAACCAGGGCCTCCCGTATGTACA A C COL3A1 Ensembl:ENSG00000168542 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:188993351..188998325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_Splice_Rec_336308,Human_Splice_Rec_336309,Human_Splice_Rec_336408,Human_Splice_Rec_336409 RMVar_hsa_circ_111421,RMVar_hsa_circ_91954,RMVar_hsa_circ_77895,RMVar_hsa_circ_205167,RMVar_hsa_circ_92152,RMVar_hsa_circ_205168,RMVar_hsa_circ_96427,RMVar_hsa_circ_118865,RMVar_hsa_circ_205171,RMVar_hsa_circ_205172,RMVar_hsa_circ_108688,RMVar_hsa_circ_98932,RMVar_hsa_circ_205174,RMVar_hsa_circ_205176,RMVar_hsa_circ_205175,RMVar_hsa_circ_205173,RMVar_hsa_circ_205184,RMVar_hsa_circ_90135,RMVar_hsa_circ_97624,RMVar_hsa_circ_87234,RMVar_hsa_circ_205187,RMVar_hsa_circ_94399,RMVar_hsa_circ_205188,RMVar_hsa_circ_92797,RMVar_hsa_circ_82843,RMVar_hsa_circ_105049,RMVar_hsa_circ_205189,RMVar_hsa_circ_119879,RMVar_hsa_circ_205192,RMVar_hsa_circ_205193,RMVar_hsa_circ_97783,RMVar_hsa_circ_205194,RMVar_hsa_circ_205198,RMVar_hsa_circ_82651,RMVar_hsa_circ_87383,RMVar_hsa_circ_205196,RMVar_hsa_circ_205197,RMVar_hsa_circ_205195,RMVar_hsa_circ_105063,RMVar_hsa_circ_124917,RMVar_hsa_circ_205201,RMVar_hsa_circ_205202,RMVar_hsa_circ_91322,RMVar_hsa_circ_205206,RMVar_hsa_circ_78566,RMVar_hsa_circ_32244,RMVar_hsa_circ_14044,RMVar_hsa_circ_60638,RMVar_hsa_circ_114363,RMVar_hsa_circ_205207,RMVar_hsa_circ_120123,RMVar_hsa_circ_205208,RMVar_hsa_circ_93210,RMVar_hsa_circ_67768,RMVar_hsa_circ_205210,RMVar_hsa_circ_205209,RMVar_hsa_circ_90813,RMVar_hsa_circ_107433,RMVar_hsa_circ_365153,RMVar_hsa_circ_89524,RMVar_hsa_circ_100141,RMVar_hsa_circ_205212,RMVar_hsa_circ_205213,RMVar_hsa_circ_205214,RMVar_hsa_circ_103732,RMVar_hsa_circ_268283,RMVar_hsa_circ_205215,RMVar_hsa_circ_205216,RMVar_hsa_circ_110057,RMVar_hsa_circ_205217 114513 RMVar_ID_114513 Human_SNP_ID_840462935 m1A Human chr2 + 54629590 54629590 54629590 CGCCCTCCCCCAGGAGCATGCCGAGTCTCCAGACGTGAGGGGCAGGCTGTCGGGCATCGAGGAGC CGCCCTCCCCCAGGAGCATGCCGAGTCTCCAGGCGTGAGGGGCAGGCTGTCGGGCATCGAGGAGC A G SPTBN1 Ensembl:ENSG00000115306 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:54629539..54629704 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 3 oesophagus Human_RBP_ID_4611546,Human_RBP_ID_8848833,Human_RBP_ID_9296523,Human_RBP_ID_22450312,Human_RBP_ID_22720653,Human_RBP_ID_22993617 Human_miRNA_ID_2150529,Human_miRNA_ID_2150530,Human_miRNA_ID_2419023,Human_miRNA_ID_2419024,Human_miRNA_ID_2791525,Human_miRNA_ID_2791526 RMVar_hsa_circ_59575,RMVar_hsa_circ_19749,RMVar_hsa_circ_111082,RMVar_hsa_circ_109985,RMVar_hsa_circ_199896,RMVar_hsa_circ_73784,RMVar_hsa_circ_114144,RMVar_hsa_circ_376090,RMVar_hsa_circ_199897,RMVar_hsa_circ_199898,RMVar_hsa_circ_67010,RMVar_hsa_circ_77414,RMVar_hsa_circ_199900,RMVar_hsa_circ_117396,RMVar_hsa_circ_374481,RMVar_hsa_circ_199902,RMVar_hsa_circ_356230,RMVar_hsa_circ_199903,RMVar_hsa_circ_367611,RMVar_hsa_circ_92406,RMVar_hsa_circ_45078,RMVar_hsa_circ_370176,RMVar_hsa_circ_199904,RMVar_hsa_circ_74935,RMVar_hsa_circ_199905,RMVar_hsa_circ_199906,RMVar_hsa_circ_199907 114514 RMVar_ID_114514 Human_SNP_ID_840466612 m1A Human chr2 - 241350116 241350110 241350116 CATCGCCATCCCCGCCCTGCATCTGCATCTGCATCTGCGCCTGCATCCTTGCAATCATCTCTTGC CATCGCCATCCCCGCCCTGCATCTGCATCTGC______GCCTGCATCCTTGCAATCATCTCTTGC CGCAGAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:241350083..241350155 26863196 MeRIP-seq:(Medium) rs772812693 Functional Loss DEL TCGA 33..38 33 UCEC 2 - 114515 RMVar_ID_114515 Human_SNP_ID_840478105 m1A Human chr2 + 241266900 241266899 241266900 ATGGTTGATCTCACACCTACACACAATCCGGGAAAACCACTAAAGCAAAGAAGAATAAATCAGAA ATGGTTGATCTCACACCTACACACAATCCGGG_AAACCACTAAAGCAAAGAAGAATAAATCAGAA GA G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,total RNA Untreated, competitive elution;HTR8/Svneo,Normoxia chr2:241266851..241266925;chr2:241266562..241267600 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 READ 1 - 114516 RMVar_ID_114516 Human_SNP_ID_840488403 m1A Human chr2 + 32618228 32618228 32618228 AAAGAATGTTTACTGAATGTTTATTTTATTTTATTTTTTTTTTACTATAGAGTGAGGGGTTGTTA AAAGAATGTTTACTGAATGTTTATTTTATTTTTTTTTTTTTTTACTATAGAGTGAGGGGTTGTTA A T BIRC6 Ensembl:ENSG00000115760 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1043463 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus Human_RBP_ID_6913393,Human_RBP_ID_8108146,Human_RBP_ID_13865580,Human_RBP_ID_24421590,Human_RBP_ID_24489161,Human_RBP_ID_27695292 RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549 114517 RMVar_ID_114517 Human_SNP_ID_840509774 m1A Human chr2 + 74460282 74460282 74460282 TACGAGGATGTGGTTCACCGCCCAGGCACACCACCCCCCCCTTATACTGTGGCCCCAGGCCGCCC TACGAGGATGTGGTTCACCGCCCAGGCACACCCCCCCCCCCTTATACTGTGGCCCCAGGCCGCCC A C WBP1,INO80B-WBP1 Ensembl:ENSG00000239779,Ensembl:ENSG00000274049 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:74460236..74460417 26863196 MeRIP-seq:(Medium) rs574091294 Functional Loss SNV ICGC,COSMIC 33..33 33 MALY,oesophagus squamous_cell_carcinoma 4 oesophagus Human_RBP_ID_555931,Human_RBP_ID_27481867,Human_RBP_ID_27564077 Human_Splice_Rec_264918,Human_Splice_Rec_264932,Human_Splice_Rec_264940,Human_Splice_Rec_264946,Human_Splice_Rec_264960,Human_Splice_Rec_264968,Human_Splice_Rec_264974,Human_Splice_Rec_264980,Human_Splice_Rec_264986,Human_Splice_Rec_264994,Human_Splice_Rec_265002,Human_Splice_Rec_265018 114518 RMVar_ID_114518 Human_SNP_ID_840517170 m1A Human chr2 + 91571490 91571490 91571490 AGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGACAGCGGCGGAGAGGCAGACAGCGGCAGCGCAG AGCGGCGGCGCGGCGGCGCGGCGGAGAGACGGCCAGCGGCGGAGAGGCAGACAGCGGCAGCGCAG A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:91571439..91571568 26863196 MeRIP-seq:(Medium) rs1194874507 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 114519 RMVar_ID_114519 Human_SNP_ID_840544406 m1A Human chr2 - 73074689 73074689 73074689 GCTTATGATTTGGGGATCAAGCCTCCATGTCTATTCTTGTTGCCTGTCCAGATGCCAAAACTCTG GCTTATGATTTGGGGATCAAGCCTCCATGTCTGTTCTTGTTGCCTGTCCAGATGCCAAAACTCTG T C SFXN5,RAB11FIP5 Ensembl:ENSG00000144040,Ensembl:ENSG00000135631 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1046183 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_13959232 GWAS_ID_13442,GWAS_ID_13443,GWAS_ID_13444 RMVar_hsa_circ_128032,RMVar_hsa_circ_201196,RMVar_hsa_circ_102179,RMVar_hsa_circ_118891,RMVar_hsa_circ_201197,RMVar_hsa_circ_201198 114520 RMVar_ID_114520 Human_SNP_ID_840590178 m1A Human chr2 - 241315975 241315975 241315975 CGGGGTACACCGGCGAGACACTCACCCGCCAAACAGCCCGAGAACAGGCGCCGACCGACCGCGCC CGGGGTACACCGGCGAGACACTCACCCGCCAACCAGCCCGAGAACAGGCGCCGACCGACCGCGCC T G HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:241315941..241316094 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,skin mycosis_fungoides-Sezary_syndrome 7 skin,haematopoietic and lymphoid tissue 114521 RMVar_ID_114521 Human_SNP_ID_840606189 m1A Human chr2 - 171160498 171160498 171160498 GCTCGCCCTCAGCGCGGCCCCCGCCATGACGGAGGCGGGTGCCGGTGCCGTTGCCGCCGCTGCCG GCTCGCCCTCAGCGCGGCCCCCGCCATGACGGGGGCGGGTGCCGGTGCCGTTGCCGCCGCTGCCG T C TLK1 Ensembl:ENSG00000198586 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr2:171160459..171160669 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_537628,Human_RBP_ID_3638208,Human_RBP_ID_5131662,Human_RBP_ID_9429370,Human_RBP_ID_17084675,Human_RBP_ID_17569336,Human_RBP_ID_18949673 RMVar_hsa_circ_127131,RMVar_hsa_circ_204598,RMVar_hsa_circ_118263,RMVar_hsa_circ_204606,RMVar_hsa_circ_125471,RMVar_hsa_circ_204610 114522 RMVar_ID_114522 Human_SNP_ID_840613824 m1A Human chr2 + 241570438 241570438 241570438 CGAGGGTACAGACGTACGGGAGGGAGTGGCGGATGGGTGAGTGTCTGAGCGCCTGGGGGGTGGGA CGAGGGTACAGACGTACGGGAGGGAGTGGCGGGTGGGTGAGTGTCTGAGCGCCTGGGGGGTGGGA A G BOK Ensembl:ENSG00000176720 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241570422..241570538 26863196 MeRIP-seq:(Medium) rs113164348 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 1 oesophagus Human_RBP_ID_8201179 RMVar_hsa_circ_84439,RMVar_hsa_circ_127107,RMVar_hsa_circ_208181,RMVar_hsa_circ_208182 114523 RMVar_ID_114523 Human_SNP_ID_840615314 m1A Human chr2 + 110672721 110672721 110672721 GTTCAGCCTGGTTTTGAATTCCTCTCTGAAGGACAGCACTGGCATGCTGCAGCTCTCCTTGGGCT GTTCAGCCTGGTTTTGAATTCCTCTCTGAAGGCCAGCACTGGCATGCTGCAGCTCTCCTTGGGCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:110669552..110672825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 114524 RMVar_ID_114524 Human_SNP_ID_840643098 m1A Human chr2 - 152657925 152657925 152657925 AAAGACAGAACTAGACAAAGATCAGAATCAAAACACAAATCGCCTAAGAAAAAGACTGGAAAGGA AAAGACAGAACTAGACAAAGATCAGAATCAAAGCACAAATCGCCTAAGAAAAAGACTGGAAAGGA T C PRPF40A Ensembl:ENSG00000196504 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:152656384..152657971 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_1900235,Human_RBP_ID_8234480,Human_RBP_ID_24546520 Human_Splice_Rec_310116,Human_Splice_Rec_310117,Human_Splice_Rec_310120,Human_Splice_Rec_310126 RMVar_hsa_circ_42443,RMVar_hsa_circ_312893,RMVar_hsa_circ_350183,RMVar_hsa_circ_360219,RMVar_hsa_circ_343598,RMVar_hsa_circ_267914,RMVar_hsa_circ_203920 114525 RMVar_ID_114525 Human_SNP_ID_840672987 m1A Human chr2 + 43224492 43224492 43224492 GCTGGGGGGCGCGTCGAACACGGGCGAGTCGGACAGGCGGCGCGGCAGCTGGAAGCTGAAGGGCG GCTGGGGGGCGCGTCGAACACGGGCGAGTCGGGCAGGCGGCGCGGCAGCTGGAAGCTGAAGGGCG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:43224276..43225025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 KIRP 1 - 114526 RMVar_ID_114526 Human_SNP_ID_840690421 m1A Human chr2 - 1660998 1660998 1660998 TTCAGGTGACAGAAAGTGGAAAATTTCACATCAGCCCTGAAGGATTCTTGACCATCAATGACGTT TTCAGGTGACAGAAAGTGGAAAATTTCACATCGGCCCTGAAGGATTCTTGACCATCAATGACGTT T C PXDN Ensembl:ENSG00000130508 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:1660947..1661081 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_Splice_Rec_210972,Human_Splice_Rec_211004,Human_Splice_Rec_211062 Human_miRNA_ID_2352674 RMVar_hsa_circ_99733,RMVar_hsa_circ_115430,RMVar_hsa_circ_91952,RMVar_hsa_circ_196616,RMVar_hsa_circ_76587,RMVar_hsa_circ_82624,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615,RMVar_hsa_circ_93700,RMVar_hsa_circ_14491,RMVar_hsa_circ_196626,RMVar_hsa_circ_111431,RMVar_hsa_circ_196627 114527 RMVar_ID_114527 Human_SNP_ID_840724104 m1A Human chr2 + 113325552 113325552 113325552 GATGGGAAGGGGAGAAACAGAAGAGTGTGACGAGGTGGGTGTCCAAGGGCAATGGGACAGGCAGT GATGGGAAGGGGAGAAACAGAAGAGTGTGACGCGGTGGGTGTCCAAGGGCAATGGGACAGGCAGT A C AC016745.1 Ensembl:ENSG00000234997 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:113325516..113325600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_290181 114528 RMVar_ID_114528 Human_SNP_ID_840765437 m1A Human chr2 - 271954 271954 271954 CCAGAGGAGTTCAGGTTGGCCTCTTTAAGATAATGAATGGTACTTACATTCTCTGAGATGTTTTG CCAGAGGAGTTCAGGTTGGCCTCTTTAAGATACTGAATGGTACTTACATTCTCTGAGATGTTTTG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:271952..272049 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate 114529 RMVar_ID_114529 Human_SNP_ID_840789035 m1A Human chr2 + 225582498 225582498 225582498 CCGACGAGTCCCCGCTTACCCCTCTGGAGGTCACGAAGCTTCCCGTGCTGGAAAACGTGTCTTAC CCGACGAGTCCCCGCTTACCCCTCTGGAGGTCGCGAAGCTTCCCGTGCTGGAAAACGTGTCTTAC A G NYAP2 Ensembl:ENSG00000144460 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:225582476..225582500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_310845,RMVar_hsa_circ_207304 114530 RMVar_ID_114530 Human_SNP_ID_840798422 m1A Human chr2 - 159783459 159783459 159783459 TGTTCTTCTTTTTTCTACATAGACTGTCCTTCATCTACTTGGATTCAGTTCCAAGACAGTTGTTA TGTTCTTCTTTTTTCTACATAGACTGTCCTTCGTCTACTTGGATTCAGTTCCAAGACAGTTGTTA T C LY75-CD302,CD302 Ensembl:ENSG00000248672,Ensembl:ENSG00000241399 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2114626 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,rectum adenocarcinoma,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 24 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_4624797 Human_Splice_Rec_312664,Human_Splice_Rec_312674,Human_Splice_Rec_312690,Human_Splice_Rec_312768,Human_Splice_Rec_312842 GWAS_ID_7467,GWAS_ID_7468,GWAS_ID_7469,GWAS_ID_7470,GWAS_ID_7471,GWAS_ID_7472,GWAS_ID_7473,GWAS_ID_7474,GWAS_ID_7475,GWAS_ID_7476,GWAS_ID_7477,GWAS_ID_7478,GWAS_ID_7479,GWAS_ID_7480,GWAS_ID_7481,GWAS_ID_7482,GWAS_ID_7483,GWAS_ID_7484,GWAS_ID_7485,GWAS_ID_7486,GWAS_ID_7487,GWAS_ID_7488,GWAS_ID_7489,GWAS_ID_7490,GWAS_ID_7491,GWAS_ID_7492,GWAS_ID_7493,GWAS_ID_7494,GWAS_ID_7495,GWAS_ID_7496,GWAS_ID_7497,GWAS_ID_7498,GWAS_ID_7499,GWAS_ID_7500,GWAS_ID_7501,GWAS_ID_7502,GWAS_ID_7503,GWAS_ID_7504,GWAS_ID_7505,GWAS_ID_7506,GWAS_ID_7507,GWAS_ID_7508,GWAS_ID_7509,GWAS_ID_7510,GWAS_ID_7511,GWAS_ID_7512,GWAS_ID_7513,GWAS_ID_7514,GWAS_ID_7515,GWAS_ID_7516,GWAS_ID_7517,GWAS_ID_7518,GWAS_ID_7519,GWAS_ID_7520,GWAS_ID_7521,GWAS_ID_7522,GWAS_ID_7523,GWAS_ID_7524,GWAS_ID_7525,GWAS_ID_7526,GWAS_ID_7527,GWAS_ID_7528,GWAS_ID_7529,GWAS_ID_7530,GWAS_ID_7531,GWAS_ID_7532,GWAS_ID_7533,GWAS_ID_7534,GWAS_ID_7535,GWAS_ID_7536,GWAS_ID_7537,GWAS_ID_7538,GWAS_ID_7539,GWAS_ID_7540,GWAS_ID_7541,GWAS_ID_7542,GWAS_ID_7543,GWAS_ID_7544,GWAS_ID_7545,GWAS_ID_7546,GWAS_ID_7547,GWAS_ID_7548,GWAS_ID_7549,GWAS_ID_7550,GWAS_ID_7551,GWAS_ID_7552,GWAS_ID_7553,GWAS_ID_7554,GWAS_ID_7555,GWAS_ID_7556,GWAS_ID_7557,GWAS_ID_7558,GWAS_ID_7559,GWAS_ID_7560,GWAS_ID_7561,GWAS_ID_7562,GWAS_ID_7563,GWAS_ID_7564,GWAS_ID_7565,GWAS_ID_7566,GWAS_ID_7567,GWAS_ID_7568,GWAS_ID_7569,GWAS_ID_7570,GWAS_ID_7571,GWAS_ID_7572,GWAS_ID_7573,GWAS_ID_7574,GWAS_ID_7575,GWAS_ID_7576,GWAS_ID_7577,GWAS_ID_7578,GWAS_ID_7579,GWAS_ID_7580,GWAS_ID_7581 RMVar_hsa_circ_353371,RMVar_hsa_circ_356989 114531 RMVar_ID_114531 Human_SNP_ID_840812512 m1A Human chr2 + 105099744 105099744 105099744 AGCCAGGCCAAGAGGGAGCCCGCAGAAAGTTTACGTGGAAGAAACGCTAAGGGTTTGCTCCCAGG AGCCAGGCCAAGAGGGAGCCCGCAGAAAGTTTCCGTGGAAGAAACGCTAAGGGTTTGCTCCCAGG A C MRPS9 Ensembl:ENSG00000135972 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:105099620..105099850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_6810492,Human_RBP_ID_9091998,Human_RBP_ID_17658583,Human_RBP_ID_17964132,Human_RBP_ID_23816430 Human_Splice_Rec_283842,Human_Splice_Rec_283858 RMVar_hsa_circ_202294,RMVar_hsa_circ_92836 114532 RMVar_ID_114532 Human_SNP_ID_840828481 m1A Human chr2 - 86032324 86032324 86032324 GGAGGGGCACATTGTGGATGCTGAAGCTGAGGAGGGGGACGCCGATGCCTCTGATGCCAAACGCA GGAGGGGCACATTGTGGATGCTGAAGCTGAGGGGGGGGACGCCGATGCCTCTGATGCCAAACGCA T C POLR1A Ensembl:ENSG00000068654 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:86031430..86033714 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate Human_RBP_ID_205271,Human_RBP_ID_827523,Human_RBP_ID_915593,Human_RBP_ID_3958003,Human_RBP_ID_5589644,Human_RBP_ID_8851361,Human_RBP_ID_9296646,Human_RBP_ID_19002055,Human_RBP_ID_26339512 Human_Splice_Rec_270350,Human_Splice_Rec_270351,Human_Splice_Rec_270416,Human_Splice_Rec_270417,Human_Splice_Rec_270432,Human_Splice_Rec_270433,Human_Splice_Rec_270438,Human_Splice_Rec_270439 RMVar_hsa_circ_116528,RMVar_hsa_circ_105967,RMVar_hsa_circ_109773,RMVar_hsa_circ_201598,RMVar_hsa_circ_201599,RMVar_hsa_circ_268456,RMVar_hsa_circ_79820,RMVar_hsa_circ_201601,RMVar_hsa_circ_201602 114533 RMVar_ID_114533 Human_SNP_ID_840831887 m1A Human chr2 - 96289086 96289086 96289086 GGAGGAGAAGCTGGAGCTGCAGAAGTTGCTGGAGAGGGTGCCTATCCCTGTAAAGGAGAGCATTG GGAGGAGAAGCTGGAGCTGCAGAAGTTGCTGGGGAGGGTGCCTATCCCTGTAAAGGAGAGCATTG T C SNRNP200 Ensembl:ENSG00000144028 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:96289026..96289125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_242928,Human_RBP_ID_830090,Human_RBP_ID_5378578,Human_RBP_ID_5589684,Human_RBP_ID_6958675,Human_RBP_ID_9384256,Human_RBP_ID_17963317,Human_RBP_ID_19002166,Human_RBP_ID_26338628 Human_Splice_Rec_274864,Human_Splice_Rec_274865,Human_Splice_Rec_274982,Human_Splice_Rec_274983,Human_Splice_Rec_275044,Human_Splice_Rec_275045 RMVar_hsa_circ_79633,RMVar_hsa_circ_88869,RMVar_hsa_circ_109508,RMVar_hsa_circ_201842,RMVar_hsa_circ_201843,RMVar_hsa_circ_98412,RMVar_hsa_circ_106511,RMVar_hsa_circ_201844,RMVar_hsa_circ_201846,RMVar_hsa_circ_201845,RMVar_hsa_circ_33767,RMVar_hsa_circ_92923,RMVar_hsa_circ_201863,RMVar_hsa_circ_84091,RMVar_hsa_circ_201865,RMVar_hsa_circ_46281 114534 RMVar_ID_114534 Human_SNP_ID_840833871 m1A Human chr2 - 45006278 45006278 45006278 CTGGGCCACCCTCCGGGCCCCAGCGCAGTGCCAGTGCCGGTGCCAGGCGGAGGTGGAGCGGACCC CTGGGCCACCCTCCGGGCCCCAGCGCAGTGCCGGTGCCGGTGCCAGGCGGAGGTGGAGCGGACCC T C SIX2 Ensembl:ENSG00000170577 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr2:45006229..45006428;chr2:45006227..45006339 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114535 RMVar_ID_114535 Human_SNP_ID_840882879 m1A Human chr2 + 191307976 191307975 191307976 CTGTTCACCAACCTAGATCCCTCCATCTCCCCAAAAAAACAGAATTGTGTTCAAATTTTTGTAAC CTGTTCACCAACCTAGATCCCTCCATCTCCCC_AAAAAACAGAATTGTGTTCAAATTTTTGTAAC CA C MYO1B Ensembl:ENSG00000128641 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:191307941..191308068 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_126354,RMVar_hsa_circ_355832,RMVar_hsa_circ_205433,RMVar_hsa_circ_357084,RMVar_hsa_circ_352897,RMVar_hsa_circ_63836,RMVar_hsa_circ_375792,RMVar_hsa_circ_205436 114536 RMVar_ID_114536 Human_SNP_ID_840883186 m1A Human chr2 - 28927652 28927652 28927652 TTCCTCTTGCTCTCTACTTGCTCGGTTTGTGGAGGAGCGGGCTTGATAGCTGCATGATGACCAGG TTCCTCTTGCTCTCTACTTGCTCGGTTTGTGGGGGAGCGGGCTTGATAGCTGCATGATGACCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:28927603..28927739 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - 114537 RMVar_ID_114537 Human_SNP_ID_840884323 m1A Human chr2 - 65268866 65268866 65268866 AAAAATTTAACAAAGCTTCCCCAAGACACCAGAATAAAACTTGACCTTTCCAGTCAAAGGGCAGA AAAAATTTAACAAAGCTTCCCCAAGACACCAGGATAAAACTTGACCTTTCCAGTCAAAGGGCAGA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:65268801..65268925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 114538 RMVar_ID_114538 Human_SNP_ID_840889938 m1A Human chr2 - 197400934 197400934 197400934 AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTAGTTGATACTACTGTGGAGTTGGCAAACAAAGT AAAGGTTTTTTGTTTTTCTGTTCTTTTTAGTTTGTTGATACTACTGTGGAGTTGGCAAACAAAGT T A SF3B1 Ensembl:ENSG00000115524 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:197400901..197400950 26863196 MeRIP-seq:(Medium) rs780559382 Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 kidney,haematopoietic and lymphoid tissue Human_RBP_ID_57610,Human_RBP_ID_4591016,Human_RBP_ID_5528137,Human_RBP_ID_6868908,Human_RBP_ID_8844489,Human_RBP_ID_18752075 Human_Splice_Rec_342072,Human_Splice_Rec_342120,Human_Splice_Rec_342168,Human_Splice_Rec_342214 RMVar_hsa_circ_67972,RMVar_hsa_circ_101657,RMVar_hsa_circ_110410,RMVar_hsa_circ_111095,RMVar_hsa_circ_107983,RMVar_hsa_circ_93312,RMVar_hsa_circ_92499,RMVar_hsa_circ_205639,RMVar_hsa_circ_205643,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_127502,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636,RMVar_hsa_circ_120089,RMVar_hsa_circ_123680,RMVar_hsa_circ_104933,RMVar_hsa_circ_86592,RMVar_hsa_circ_205649,RMVar_hsa_circ_205651,RMVar_hsa_circ_205652,RMVar_hsa_circ_205650,RMVar_hsa_circ_346958,RMVar_hsa_circ_82724,RMVar_hsa_circ_205654,RMVar_hsa_circ_205655,RMVar_hsa_circ_79158,RMVar_hsa_circ_40892,RMVar_hsa_circ_205656,RMVar_hsa_circ_3015,RMVar_hsa_circ_268639 114539 RMVar_ID_114539 Human_SNP_ID_840899339 m1A Human chr2 - 19898113 19898113 19898113 ATGCTGCATGTTATAGGCTGTGAAGTTTGACAATACCCAAAAGAGAATGAAAGTGGAAATGAGAG ATGCTGCATGTTATAGGCTGTGAAGTTTGACAGTACCCAAAAGAGAATGAAAGTGGAAATGAGAG T C TTC32 Ensembl:ENSG00000183891 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12328613 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_13734058,Human_RBP_ID_23846720 GWAS_ID_11167,GWAS_ID_11168,GWAS_ID_11169,GWAS_ID_11170,GWAS_ID_11171 114540 RMVar_ID_114540 Human_SNP_ID_840936866 m1A Human chr2 + 27234626 27234626 27234626 TGGACCTAGTAGCCTTGGCCACGCGGGTCATCATGGGGGAAGAAGTGGAACCTGTGGGGCTAATG TGGACCTAGTAGCCTTGGCCACGCGGGTCATCGTGGGGGAAGAAGTGGAACCTGTGGGGCTAATG A G CAD Ensembl:ENSG00000084774 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:27234580..27234699 26863196 MeRIP-seq:(Medium) rs767776598 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_56853,Human_RBP_ID_8847482,Human_RBP_ID_22991465,Human_RBP_ID_26819605 Human_Splice_Rec_227591,Human_Splice_Rec_227675,Human_Splice_Rec_227731 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_197930,RMVar_hsa_circ_197929,RMVar_hsa_circ_7687,RMVar_hsa_circ_197937,RMVar_hsa_circ_83115,RMVar_hsa_circ_87533,RMVar_hsa_circ_77235,RMVar_hsa_circ_197938,RMVar_hsa_circ_197936,RMVar_hsa_circ_93360,RMVar_hsa_circ_80057,RMVar_hsa_circ_197941,RMVar_hsa_circ_97567,RMVar_hsa_circ_197945,RMVar_hsa_circ_76373,RMVar_hsa_circ_197946,RMVar_hsa_circ_197944,RMVar_hsa_circ_86946,RMVar_hsa_circ_119746,RMVar_hsa_circ_101201,RMVar_hsa_circ_30423,RMVar_hsa_circ_197948,RMVar_hsa_circ_197950,RMVar_hsa_circ_197952,RMVar_hsa_circ_99512,RMVar_hsa_circ_108844,RMVar_hsa_circ_197953,RMVar_hsa_circ_197954,RMVar_hsa_circ_268035 114541 RMVar_ID_114541 Human_SNP_ID_840951161 m1A Human chr2 - 189002975 189002975 189002975 TTCTCACCCGGAGCCCCTCTTTCTCCTTTACCACCAGGTTCACCATTCTGTCCCTACATGCAACA TTCTCACCCGGAGCCCCTCTTTCTCCTTTACCGCCAGGTTCACCATTCTGTCCCTACATGCAACA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:188999326..189003075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus 114542 RMVar_ID_114542 Human_SNP_ID_840970895 m1A Human chr2 - 47170760 47170760 47170760 CTAACCTTCCTCTTTGATCTCTTTGTAGGCTGACCAACTGACTGAAGAGCAGATTGCAGGTGAGA CTAACCTTCCTCTTTGATCTCTTTGTAGGCTGCCCAACTGACTGAAGAGCAGATTGCAGGTGAGA T G CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:47170726..47170775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_243738,Human_RBP_ID_777130,Human_RBP_ID_1587373,Human_RBP_ID_2649326,Human_RBP_ID_4623284,Human_RBP_ID_6927068,Human_RBP_ID_9331004,Human_RBP_ID_9383600,Human_RBP_ID_13905806,Human_RBP_ID_19097375,Human_RBP_ID_22452173,Human_RBP_ID_22478042,Human_RBP_ID_22595250,Human_RBP_ID_22670057,Human_RBP_ID_22742948,Human_RBP_ID_23874728,Human_RBP_ID_26339261,Human_RBP_ID_27817062 Human_Splice_Rec_242756,Human_Splice_Rec_242757,Human_Splice_Rec_242772,Human_Splice_Rec_242773,Human_Splice_Rec_242782,Human_Splice_Rec_242783,Human_Splice_Rec_242788,Human_Splice_Rec_242789,Human_Splice_Rec_242797,Human_Splice_Rec_242806,Human_Splice_Rec_242807,Human_Splice_Rec_242816,Human_Splice_Rec_242817,Human_Splice_Rec_242826,Human_Splice_Rec_242827,Human_Splice_Rec_242836,Human_Splice_Rec_242837,Human_Splice_Rec_242854,Human_Splice_Rec_242855,Human_Splice_Rec_242864,Human_Splice_Rec_242865,Human_Splice_Rec_242874,Human_Splice_Rec_242875,Human_Splice_Rec_242890,Human_Splice_Rec_242891,Human_Splice_Rec_242904,Human_Splice_Rec_242905,Human_Splice_Rec_242914,Human_Splice_Rec_242915 Human_miRNA_ID_2244974 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 114543 RMVar_ID_114543 Human_SNP_ID_840997408 m1A Human chr2 - 130342046 130342046 130342046 GCTGCTTGGGGACCTGGAGGAGCTGGAGGGGAAACGAACGGTGTTGAACGCCCGGGTGGAGGAGG GCTGCTTGGGGACCTGGAGGAGCTGGAGGGGACACGAACGGTGTTGAACGCCCGGGTGGAGGAGG T G CCDC115 Ensembl:ENSG00000136710 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:130342032..130342118 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 GBM 1 - Human_RBP_ID_4623620,Human_RBP_ID_5322192,Human_RBP_ID_22996869 Human_Splice_Rec_297037,Human_Splice_Rec_297045 114544 RMVar_ID_114544 Human_SNP_ID_840999457 m1A Human chr2 + 73252872 73252872 73252872 TGGTCGTGGCCGCCCCCACTGAGAGGCACCCCACCCATCACATGGCTGGCTGGCTGCTGGGTGCA TGGTCGTGGCCGCCCCCACTGAGAGGCACCCCGCCCATCACATGGCTGGCTGGCTGCTGGGTGCA A G CCT7 Ensembl:ENSG00000135624 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr2:73252821..73252921 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_555273,Human_RBP_ID_775679,Human_RBP_ID_4634383,Human_RBP_ID_6948330,Human_RBP_ID_8525002,Human_RBP_ID_8849732,Human_RBP_ID_9296615,Human_RBP_ID_14027435,Human_RBP_ID_17657628,Human_RBP_ID_17961018,Human_RBP_ID_18193328,Human_RBP_ID_18768369,Human_RBP_ID_22449857,Human_RBP_ID_26488560,Human_RBP_ID_27292206 RMVar_hsa_circ_201217,RMVar_hsa_circ_94853 114545 RMVar_ID_114545 Human_SNP_ID_841028297 m1A Human chr2 - 241633796 241633796 241633796 GGGGTGTGAGGGGACACTCGAGTGCCGCCACCAGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG GGGGTGTGAGGGGACACTCGAGTGCCGCCACCGGCAGAGGAGCTGCAGGTTGGTCACCGTCCTCG T C THAP4 Ensembl:ENSG00000176946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:241633746..241634100 26863196 MeRIP-seq:(Medium) rs7424328 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,large_intestine adenocarcinoma 3 head and neck,large intestine Human_RBP_ID_4625286,Human_RBP_ID_17965088,Human_RBP_ID_19001057 Human_miRNA_ID_2050651 RMVar_hsa_circ_208185,RMVar_hsa_circ_353733,RMVar_hsa_circ_338904,RMVar_hsa_circ_273583,RMVar_hsa_circ_342575,RMVar_hsa_circ_208191 114546 RMVar_ID_114546 Human_SNP_ID_841049880 m1A Human chr2 - 38751333 38751333 38751333 CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGTAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC T A SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs182579979 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_58102,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2428154,Human_miRNA_ID_2487953,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 114547 RMVar_ID_114547 Human_SNP_ID_841049882 m1A Human chr2 - 38751333 38751333 38751333 CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGAAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC CCTCGTAGTGCCGCCGGGACTCTTGGCGGGTGGAGGTGTGTGTCAGCTTTTGCGTCACTCGAGCC T C SRSF7 Ensembl:ENSG00000115875 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs182579979 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,UCEC,ESCA,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 9 uterus,large intestine Human_RBP_ID_58102,Human_RBP_ID_4623252,Human_RBP_ID_5275561,Human_RBP_ID_9330424,Human_RBP_ID_18421745,Human_RBP_ID_22452151,Human_RBP_ID_23871181,Human_RBP_ID_26818408,Human_RBP_ID_27011645,Human_RBP_ID_27840018 Human_miRNA_ID_2405133,Human_miRNA_ID_2408128,Human_miRNA_ID_2411121,Human_miRNA_ID_2414100,Human_miRNA_ID_2428154,Human_miRNA_ID_2487953,Human_miRNA_ID_2622611 RMVar_hsa_circ_104000,RMVar_hsa_circ_199041,RMVar_hsa_circ_111155,RMVar_hsa_circ_199044 114548 RMVar_ID_114548 Human_SNP_ID_841061302 m1A Human chr2 - 45652121 45652118 45652121 AAGCTCACGGCCTCGCAGATTTTGATCTTAAGAAGGCCATTGAACACTACCATGGTCGGGGCGGG AAGCTCACGGCCTCGCAGATTTTGATCTTAAG___GCCATTGAACACTACCATGGTCGGGGCGGG CCTT C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr2:45652074..45652210 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 BRCA 1 - 114549 RMVar_ID_114549 Human_SNP_ID_841063889 m1A Human chr2 - 240524178 240524178 240524178 TTCCAGGACACCGGGCAGTGTGGGGGGTCCATAGACCACAGGAGCAGCTCTCTGAAGGGGGACTC TTCCAGGACACCGGGCAGTGTGGGGGGTCCATGGACCACAGGAGCAGCTCTCTGAAGGGGGACTC T C ANKMY1 Ensembl:ENSG00000144504 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35996697 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,thyroid neoplasm,COCA 19 head and neck,prostate GWAS_ID_7636 RMVar_hsa_circ_207965,RMVar_hsa_circ_92801,RMVar_hsa_circ_330191,RMVar_hsa_circ_337796,RMVar_hsa_circ_4972,RMVar_hsa_circ_341953,RMVar_hsa_circ_347733,RMVar_hsa_circ_207964,RMVar_hsa_circ_53903,RMVar_hsa_circ_93116,RMVar_hsa_circ_36644,RMVar_hsa_circ_59311,RMVar_hsa_circ_366073,RMVar_hsa_circ_29790,RMVar_hsa_circ_373861,RMVar_hsa_circ_207970,RMVar_hsa_circ_107477,RMVar_hsa_circ_207971,RMVar_hsa_circ_316676,RMVar_hsa_circ_368315,RMVar_hsa_circ_207972,RMVar_hsa_circ_323613,RMVar_hsa_circ_303441,RMVar_hsa_circ_207973,RMVar_hsa_circ_207974 114550 RMVar_ID_114550 Human_SNP_ID_841089564 m1A Human chr2 - 210591924 210591924 210591924 TCGTTGACATTCACAAAAAGTGGTTTCCAGCCAGCAGGGAGGGTGTTGTCCAAGGCATAGCCATG TCGTTGACATTCACAAAAAGTGGTTTCCAGCCTGCAGGGAGGGTGTTGTCCAAGGCATAGCCATG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr2:210591874..210592009 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung 114551 RMVar_ID_114551 Human_SNP_ID_841102042 m1A Human chr2 + 158457094 158457094 158457094 AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGGAGGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC AGAGCCGCTCCGGGGGCGGGGGCCGGTGGGGGGGGGAGGGGCGGGCAGCCGCGCCGCCGCGGCAC A G PKP4 Ensembl:ENSG00000144283 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr2:158456970..158457099 26863196 MeRIP-seq:(Medium) rs976473870 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3638184,Human_RBP_ID_4622725,Human_RBP_ID_5239673,Human_RBP_ID_5322655,Human_RBP_ID_5381702,Human_RBP_ID_8200720,Human_RBP_ID_8728732,Human_RBP_ID_9330702,Human_RBP_ID_9428843,Human_RBP_ID_18948334,Human_RBP_ID_20615816,Human_RBP_ID_22596441,Human_RBP_ID_24553139,Human_RBP_ID_26787214 114552 RMVar_ID_114552 Human_SNP_ID_841109145 m1A Human chr2 + 233428112 233428112 233428112 CCAGAGGTTGGGCTGTGGCTGGTGTTAGGGGAACAGGAGTAGGAGGGGAGCCAGAGGAGGAGGAG CCAGAGGTTGGGCTGTGGCTGGTGTTAGGGGAGCAGGAGTAGGAGGGGAGCCAGAGGAGGAGGAG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr2:233428105..233428267 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_99963,RMVar_hsa_circ_109505,RMVar_hsa_circ_207719,RMVar_hsa_circ_25931,RMVar_hsa_circ_339725,RMVar_hsa_circ_207722 114553 RMVar_ID_114553 Human_SNP_ID_841116065 m1A Human chr2 + 232456361 232456361 232456361 TCTACTCTCCCCCTGGCCAGCTGAGGAGGAGAACCCGGCCTTCTGGAACCGCCAGGCAGCTGAGG TCTACTCTCCCCCTGGCCAGCTGAGGAGGAGAGCCCGGCCTTCTGGAACCGCCAGGCAGCTGAGG A G ALPI Ensembl:ENSG00000163295 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr2:232456126..232456373 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_5589101,Human_RBP_ID_27158447,Human_RBP_ID_27478320 Human_Splice_Rec_370728 114554 RMVar_ID_114554 Human_SNP_ID_841123363 m1A Human chr2 - 240455006 240455006 240455006 AGCCTTAACTTTGGATACCTTTTAGGTCATGCATTCTCGTCCCCTGCTGACATGTCCCCACCCCG AGCCTTAACTTTGGATACCTTTTAGGTCATGCCTTCTCGTCCCCTGCTGACATGTCCCCACCCCG T G AC110619.1 Ensembl:ENSG00000218416 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr2:240454957..240455041 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114555 RMVar_ID_114555 Human_SNP_ID_841136440 m1A Human chr2 + 233463375 233463375 233463375 CGCATCTCACTCCACACATCACCTCACTCCACACATCTCCTCACTCCACACATCTCCTCACTCCA CGCATCTCACTCCACACATCACCTCACTCCACGCATCTCCTCACTCCACACATCTCCTCACTCCA A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr2:233463325..233463413 26863196 MeRIP-seq:(Medium) rs1255106564 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_205531,Human_RBP_ID_2627948 RMVar_hsa_circ_114993,RMVar_hsa_circ_207728,RMVar_hsa_circ_32498,RMVar_hsa_circ_32447 114556 RMVar_ID_114556 Human_SNP_ID_856748543 m1A Human chr5 + 168506820 168506820 168506820 CGAGTCTTCCATGCTGGATTTGGTGTGGTGCTAGGGGAAGACAAGTAAGTCTGGAAAATCTGAAG CGAGTCTTCCATGCTGGATTTGGTGTGGTGCTGGGGGAAGACAAGTAAGTCTGGAAAATCTGAAG A G RARS1 Ensembl:ENSG00000113643 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168506771..168506875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_RBP_ID_7413138,Human_RBP_ID_8887720,Human_RBP_ID_22460309,Human_RBP_ID_24094858 Human_Splice_Rec_718606,Human_Splice_Rec_718607,Human_Splice_Rec_718650,Human_Splice_Rec_718651 Human_miRNA_ID_2299844,Human_miRNA_ID_2303112,Human_miRNA_ID_2306376 RMVar_hsa_circ_124053,RMVar_hsa_circ_305517,RMVar_hsa_circ_236012,RMVar_hsa_circ_236013,RMVar_hsa_circ_351023,RMVar_hsa_circ_314446,RMVar_hsa_circ_275213,RMVar_hsa_circ_272045,RMVar_hsa_circ_236023,RMVar_hsa_circ_236024,RMVar_hsa_circ_236022,RMVar_hsa_circ_90623,RMVar_hsa_circ_236025,RMVar_hsa_circ_364584,RMVar_hsa_circ_79536,RMVar_hsa_circ_96588,RMVar_hsa_circ_236030,RMVar_hsa_circ_103677,RMVar_hsa_circ_363003,RMVar_hsa_circ_236026,RMVar_hsa_circ_302180,RMVar_hsa_circ_236028,RMVar_hsa_circ_276326,RMVar_hsa_circ_284618,RMVar_hsa_circ_307188,RMVar_hsa_circ_236032,RMVar_hsa_circ_236031,RMVar_hsa_circ_74786,RMVar_hsa_circ_236029,RMVar_hsa_circ_295204,RMVar_hsa_circ_361471,RMVar_hsa_circ_368026,RMVar_hsa_circ_358377,RMVar_hsa_circ_127973,RMVar_hsa_circ_236035,RMVar_hsa_circ_236037,RMVar_hsa_circ_236038,RMVar_hsa_circ_236036,RMVar_hsa_circ_236039 114557 RMVar_ID_114557 Human_SNP_ID_856767114 m1A Human chr5 + 32143852 32143852 32143852 CAATTAACATACAGCCACGTAATCCAGATGATATACAGTCATTCCAAAATGATGTGTAACCCTAT CAATTAACATACAGCCACGTAATCCAGATGATTTACAGTCATTCCAAAATGATGTGTAACCCTAT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:32143801..32143900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 114558 RMVar_ID_114558 Human_SNP_ID_856770686 m1A Human chr5 - 181188869 181188869 181188869 TCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAAATCCCGGACGAGCCCACTTTTTCATTTTTTTT TCTCGCTTTGGGTGCGAGAGGTCCCGGGTTCAGATCCCGGACGAGCCCACTTTTTCATTTTTTTT T C LINC01962 Ensembl:ENSG00000248473 lincRNA intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_1244571,Human_RBP_ID_1652838,Human_RBP_ID_5449739,Human_RBP_ID_7425806,Human_RBP_ID_8267516,Human_RBP_ID_15416751,Human_RBP_ID_17584813,Human_RBP_ID_18840630,Human_RBP_ID_23050504,Human_RBP_ID_23136943,Human_RBP_ID_24508997,Human_RBP_ID_27335966 114559 RMVar_ID_114559 Human_SNP_ID_856772475 m1A Human chr5 + 76242367 76242367 76242367 GCGGGACGCAGCGGCGCGCGGGCTTTGGTCGGACCGGGGGTCGTTCTCGCCTCTTCTTCACACTG GCGGGACGCAGCGGCGCGCGGGCTTTGGTCGGTCCGGGGGTCGTTCTCGCCTCTTCTTCACACTG A T SV2C Ensembl:ENSG00000122012 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:76242267..76242385 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_95491,RMVar_hsa_circ_344778,RMVar_hsa_circ_232574,RMVar_hsa_circ_81833,RMVar_hsa_circ_232575,RMVar_hsa_circ_232573 114560 RMVar_ID_114560 Human_SNP_ID_856810333 m1A Human chr5 - 95555188 95555186 95555189 TCCCTAGCAGAGCAGGGCAGGGACAGCGAACAACTCCCAAAGCTTGCAGTTTGGTTGCTTGATAG TCCCTAGCAGAGCAGGGCAGGGACAGCGAAC___TCCCAAAGCTTGCAGTTTGGTTGCTTGATAG AGTT A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:95555139..95555225 26863196 MeRIP-seq:(Medium) rs1470129761 Functional Loss DEL ICGC 32..34 33 STAD 1 - 114561 RMVar_ID_114561 Human_SNP_ID_856833386 m1A Human chr5 + 10254822 10254822 10254822 TCCAAGTCTCAGGATGATGAAATTGGAGATGGAACCACAGGAGTGGTTGGTAAGAAAAGACAAAA TCCAAGTCTCAGGATGATGAAATTGGAGATGGGACCACAGGAGTGGTTGGTAAGAAAAGACAAAA A G CCT5 Ensembl:ENSG00000150753 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:10254636..10254883 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_946949,Human_RBP_ID_1642165,Human_RBP_ID_1982844,Human_RBP_ID_8893449,Human_RBP_ID_9306384,Human_RBP_ID_9397627,Human_RBP_ID_15249683,Human_RBP_ID_17706499,Human_RBP_ID_18056707,Human_RBP_ID_19014721,Human_RBP_ID_19124310,Human_RBP_ID_22458797,Human_RBP_ID_24536131,Human_RBP_ID_27826235 Human_Splice_Rec_634899,Human_Splice_Rec_634934,Human_Splice_Rec_634935,Human_Splice_Rec_634943,Human_Splice_Rec_634984,Human_Splice_Rec_634985,Human_Splice_Rec_634995 Human_miRNA_ID_2708063 RMVar_hsa_circ_25255,RMVar_hsa_circ_230206,RMVar_hsa_circ_91562,RMVar_hsa_circ_230207,RMVar_hsa_circ_120671,RMVar_hsa_circ_378948,RMVar_hsa_circ_23810,RMVar_hsa_circ_84186,RMVar_hsa_circ_100741,RMVar_hsa_circ_230209,RMVar_hsa_circ_12690,RMVar_hsa_circ_230208 114562 RMVar_ID_114562 Human_SNP_ID_856834611 m1A Human chr5 - 177483502 177483502 177483502 GCCCGAGCCTGGGGCTCCCTGGGCCCTGCCCCACCCACCTTATCCTCCCACCCCACTCCCTCCAC GCCCGAGCCTGGGGCTCCCTGGGCCCTGCCCCCCCCACCTTATCCTCCCACCCCACTCCCTCCAC T G PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:177483451..177483725 26863196 MeRIP-seq:(Medium) rs1448648328 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_165994,Human_RBP_ID_17090152,Human_RBP_ID_18956307,Human_RBP_ID_27079162 Human_miRNA_ID_1705278 RMVar_hsa_circ_101676,RMVar_hsa_circ_123362,RMVar_hsa_circ_236506,RMVar_hsa_circ_236507 114563 RMVar_ID_114563 Human_SNP_ID_856850193 m1A Human chr5 - 112891953 112891953 112891953 ATTGTTCCTTTAACTTTCTCTCTTGTTCTTCTAGCCATTTTTTAGCCGCCTCTTCCTTTTCCTTC ATTGTTCCTTTAACTTTCTCTCTTGTTCTTCTTGCCATTTTTTAGCCGCCTCTTCCTTTTCCTTC T A REEP5 Ensembl:ENSG00000129625 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:112891785..112892102 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_21213969 RMVar_hsa_circ_233794,RMVar_hsa_circ_104264,RMVar_hsa_circ_344625 114564 RMVar_ID_114564 Human_SNP_ID_856857806 m1A Human chr5 + 392443 392443 392443 GCGTGCACGAACACACGGGTGCAGGGCGAGGCAGGCGCAGGGCGAGGCAGGGCCAGAGTGTGCAC GCGTGCACGAACACACGGGTGCAGGGCGAGGCGGGCGCAGGGCGAGGCAGGGCCAGAGTGTGCAC A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:392438..392547 26863196 MeRIP-seq:(Medium) rs1431855442 Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_17299,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_329311,RMVar_hsa_circ_110112,RMVar_hsa_circ_49287,RMVar_hsa_circ_229950,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_229952 114565 RMVar_ID_114565 Human_SNP_ID_856911761 m1A Human chr5 - 173321537 173321537 173321537 TCCTAGACCTGAAAGGGCTCACAGCTCCCCACATGTGGTGGGCTTCTTGTCCTTTTATCAAATAT TCCTAGACCTGAAAGGGCTCACAGCTCCCCACCTGTGGTGGGCTTCTTGTCCTTTTATCAAATAT T G STC2 Ensembl:ENSG00000113739 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4867699 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_637890 GWAS_ID_7687,GWAS_ID_7688 RMVar_hsa_circ_236294,RMVar_hsa_circ_116248,RMVar_hsa_circ_80495,RMVar_hsa_circ_236295 114566 RMVar_ID_114566 Human_SNP_ID_856929353 m1A Human chr5 - 138172112 138172112 138172112 CATTTTGTAGGGTATCAGTTAGCAGAGCAATCAAGCCCTTTGCAGAACCTGGCCGCCCTCCAGAC CATTTTGTAGGGTATCAGTTAGCAGAGCAATCGAGCCCTTTGCAGAACCTGGCCGCCCTCCAGAC T C BRD8 Ensembl:ENSG00000112983 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138171407..138172747 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_942985,Human_RBP_ID_3758693,Human_RBP_ID_3967422,Human_RBP_ID_4810748,Human_RBP_ID_5395695,Human_RBP_ID_15311563 Human_Splice_Rec_695380,Human_Splice_Rec_695381,Human_Splice_Rec_695446,Human_Splice_Rec_695447,Human_Splice_Rec_695484,Human_Splice_Rec_695485,Human_Splice_Rec_695524,Human_Splice_Rec_695525,Human_Splice_Rec_695562,Human_Splice_Rec_695563,Human_Splice_Rec_695604,Human_Splice_Rec_695605,Human_Splice_Rec_695644,Human_Splice_Rec_695645,Human_Splice_Rec_695784,Human_Splice_Rec_695785,Human_Splice_Rec_695800,Human_Splice_Rec_695801,Human_Splice_Rec_695814,Human_Splice_Rec_695815,Human_Splice_Rec_695830,Human_Splice_Rec_695831,Human_Splice_Rec_695842,Human_Splice_Rec_695843,Human_Splice_Rec_695854,Human_Splice_Rec_695855 RMVar_hsa_circ_35412,RMVar_hsa_circ_53438 114567 RMVar_ID_114567 Human_SNP_ID_856951377 m1A Human chr5 + 78294562 78294561 78294562 GCCTCCCCTCCTCCGGACTGCTCATTGTAAGGAAAACTATTGCTGGACATTGCCGCGGTGCTGGC GCCTCCCCTCCTCCGGACTGCTCATTGTAAGG_AAACTATTGCTGGACATTGCCGCGGTGCTGGC GA G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:78294511..78294681 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - 114568 RMVar_ID_114568 Human_SNP_ID_856963905 m1A Human chr5 - 176532110 176532110 176532110 ACCCTCCCAGCAGCCGCCGTCCCGACCTCCACACCTCCCCGTAGAGGAGCGCCGAGCCTCGGCTC ACCCTCCCAGCAGCCGCCGTCCCGACCTCCACCCCTCCCCGTAGAGGAGCGCCGAGCCTCGGCTC T G RNF44 Ensembl:ENSG00000146083 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176531988..176532237 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - Human_RBP_ID_788789,Human_RBP_ID_4853106,Human_RBP_ID_5449665,Human_RBP_ID_27842127 Human_Splice_Rec_723140,Human_Splice_Rec_723168,Human_Splice_Rec_723194 114569 RMVar_ID_114569 Human_SNP_ID_856980762 m1A Human chr5 - 177961655 177961655 177961655 GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAATGTCAGCCATGGCCATCGTTCCCTCTGCCACG GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCACTGTCAGCCATGGCCATCGTTCCCTCTGCCACG T G RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525,lnc-PROP1-2:3 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0,RNACentral:URS00008B2D92 SRP RNA,lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961649..177961740 26863196 MeRIP-seq:(Medium) rs11743951 Functional Loss SNV ICGC 33..33 33 OV 1 - 114570 RMVar_ID_114570 Human_SNP_ID_856980768 m1A Human chr5 - 177961655 177961655 177961655 GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAATGTCAGCCATGGCCATCGTTCCCTCTGCCACG GGCCATCGTTCCCTCTGCCAGCTCCCTCCTCAGTGTCAGCCATGGCCATCGTTCCCTCTGCCACG T C RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525,lnc-PROP1-2:3 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0,RNACentral:URS00008B2D92 SRP RNA,lincRNA,lincRNA,SRP RNA,lincRNA intron,intron,intron,intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961649..177961740 26863196 MeRIP-seq:(Medium) rs11743951 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 114571 RMVar_ID_114571 Human_SNP_ID_857043779 m1A Human chr5 - 94618723 94618723 94618723 TCTGGGATGCTTCCTTCGGTGGCAGCGGCGGCAGGGGCGACGACTGCCGCTGCAGCACTCAACTG TCTGGGATGCTTCCTTCGGTGGCAGCGGCGGCGGGGGCGACGACTGCCGCTGCAGCACTCAACTG T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:94618676..94618810;chr5:94618676..94618824 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114572 RMVar_ID_114572 Human_SNP_ID_857046434 m1A Human chr5 + 85479 85479 85479 TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACATACGCAGGAGGGAGG TGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGGGAGGCAGCGAGCAGACATACGCAGGAGGGAGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:85477..85568 26863196 MeRIP-seq:(Medium) rs117925003 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 114573 RMVar_ID_114573 Human_SNP_ID_857102483 m1A Human chr5 + 168378942 168378942 168378942 CGGCGTGGGTGTGTATGCAGTGTGGAGAAAACAGGTGTGTGGCAAGTGTAGGAAGGGATGGGTGT CGGCGTGGGTGTGTATGCAGTGTGGAGAAAACTGGTGTGTGGCAAGTGTAGGAAGGGATGGGTGT A T WWC1 Ensembl:ENSG00000113645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:168378941..168379057 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_235991,RMVar_hsa_circ_103063,RMVar_hsa_circ_235993,RMVar_hsa_circ_288453,RMVar_hsa_circ_351327,RMVar_hsa_circ_235994 114574 RMVar_ID_114574 Human_SNP_ID_857112185 m1A Human chr5 + 33162282 33162282 33162282 GCGGAAGTATGAGTTGGAGCGCCCAGCTGCCAACACCAAGATTGGCCCCCGCCGCATCCACACAG GCGGAAGTATGAGTTGGAGCGCCCAGCTGCCACCACCAAGATTGGCCCCCGCCGCATCCACACAG A C AC010343.1 Ensembl:ENSG00000240376 Pseudogene exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:33162204..33162293 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THCA 1 - Human_RBP_ID_641341,Human_RBP_ID_1994607,Human_RBP_ID_5103923,Human_RBP_ID_8268648,Human_RBP_ID_9183865,Human_RBP_ID_17416752,Human_RBP_ID_18057957,Human_RBP_ID_22404040 Human_miRNA_ID_1904700 114575 RMVar_ID_114575 Human_SNP_ID_857132570 m1A Human chr5 - 176355612 176355612 176355612 CTCCTCCATCGGACATGGGCAGCGTCCCTTGGAAGCCAGTGATTCCAGAGCGCAAGTATCAGCAC CTCCTCCATCGGACATGGGCAGCGTCCCTTGGGAGCCAGTGATTCCAGAGCGCAAGTATCAGCAC T C KIAA1191 Ensembl:ENSG00000122203 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176355576..176355725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_638254,Human_RBP_ID_15389618,Human_RBP_ID_23116285,Human_RBP_ID_26827664 Human_Splice_Rec_722867,Human_Splice_Rec_722881,Human_Splice_Rec_722893,Human_Splice_Rec_722917,Human_Splice_Rec_722937,Human_Splice_Rec_722947,Human_Splice_Rec_722951,Human_Splice_Rec_722959 RMVar_hsa_circ_14792,RMVar_hsa_circ_236358,RMVar_hsa_circ_112696,RMVar_hsa_circ_236356,RMVar_hsa_circ_96878,RMVar_hsa_circ_271924,RMVar_hsa_circ_236360,RMVar_hsa_circ_370777,RMVar_hsa_circ_236357,RMVar_hsa_circ_279654,RMVar_hsa_circ_236359 114576 RMVar_ID_114576 Human_SNP_ID_857194249 m1A Human chr5 + 96803622 96803622 96803622 CTCCAGCTCCCTTCCTGAGGGTGGCCCTAGATATCTGCAGGTGGTGACTATGCAGGATGATGGTG CTCCAGCTCCCTTCCTGAGGGTGGCCCTAGATGTCTGCAGGTGGTGACTATGCAGGATGATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:96803572..96803652 26863196 MeRIP-seq:(Medium) rs1449075742 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114577 RMVar_ID_114577 Human_SNP_ID_857204583 m1A Human chr5 - 69167285 69167285 69167285 AGGCCGCGTTAGTTCGCAGTCCGAAGCGGCTCACCCTGGTGACTCGGAGCGCCATGGCTTCCTCT AGGCCGCGTTAGTTCGCAGTCCGAAGCGGCTCGCCCTGGTGACTCGGAGCGCCATGGCTTCCTCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:69167126..69167345 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114578 RMVar_ID_114578 Human_SNP_ID_857223996 m1A Human chr5 + 112922177 112922177 112922177 TCTCGTGCAGGAACCGGTCGAACCTCTCCCTCATGGCCGCAGACATGGCGGGGACCGTCTCGCCG TCTCGTGCAGGAACCGGTCGAACCTCTCCCTCGTGGCCGCAGACATGGCGGGGACCGTCTCGCCG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:112922126..112922275;chr5:112922126..112922280;chr5:112922126..112922278 26863196 MeRIP-seq:(Medium) rs780984444 Functional Loss SNV TCGA 33..33 33 THYM 1 - 114579 RMVar_ID_114579 Human_SNP_ID_857227123 m1A Human chr5 + 14296140 14296140 14296140 AGAGGGGTTGTGTGGGAAGTGAGAGAAGGGGGAAAAACGTAGGGAAGTTTGGACAGATCAGGAAA AGAGGGGTTGTGTGGGAAGTGAGAGAAGGGGGGAAAACGTAGGGAAGTTTGGACAGATCAGGAAA A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:14295983..14296235 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_283,RMVar_hsa_circ_79613,RMVar_hsa_circ_230323,RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_291585,RMVar_hsa_circ_323713,RMVar_hsa_circ_341444,RMVar_hsa_circ_347025,RMVar_hsa_circ_344313,RMVar_hsa_circ_324581,RMVar_hsa_circ_315318,RMVar_hsa_circ_122686,RMVar_hsa_circ_230329,RMVar_hsa_circ_230331,RMVar_hsa_circ_230333,RMVar_hsa_circ_72119,RMVar_hsa_circ_230334,RMVar_hsa_circ_230332,RMVar_hsa_circ_230330,RMVar_hsa_circ_230327,RMVar_hsa_circ_230328,RMVar_hsa_circ_296611,RMVar_hsa_circ_64523,RMVar_hsa_circ_311291,RMVar_hsa_circ_372445,RMVar_hsa_circ_323300,RMVar_hsa_circ_300557,RMVar_hsa_circ_48236,RMVar_hsa_circ_230336,RMVar_hsa_circ_230337,RMVar_hsa_circ_230338,RMVar_hsa_circ_328078,RMVar_hsa_circ_230335,RMVar_hsa_circ_371911,RMVar_hsa_circ_298615,RMVar_hsa_circ_119805,RMVar_hsa_circ_288034,RMVar_hsa_circ_104964,RMVar_hsa_circ_51064,RMVar_hsa_circ_25150,RMVar_hsa_circ_6202,RMVar_hsa_circ_33778,RMVar_hsa_circ_230341,RMVar_hsa_circ_230343,RMVar_hsa_circ_230345,RMVar_hsa_circ_230346,RMVar_hsa_circ_230344,RMVar_hsa_circ_230342,RMVar_hsa_circ_230340,RMVar_hsa_circ_279668,RMVar_hsa_circ_290370,RMVar_hsa_circ_321654,RMVar_hsa_circ_322157,RMVar_hsa_circ_354676,RMVar_hsa_circ_297245,RMVar_hsa_circ_284160,RMVar_hsa_circ_48759,RMVar_hsa_circ_87690,RMVar_hsa_circ_42825,RMVar_hsa_circ_230348,RMVar_hsa_circ_5235,RMVar_hsa_circ_21682,RMVar_hsa_circ_230350,RMVar_hsa_circ_230351,RMVar_hsa_circ_230352,RMVar_hsa_circ_230349,RMVar_hsa_circ_276760,RMVar_hsa_circ_278990,RMVar_hsa_circ_323820,RMVar_hsa_circ_230347,RMVar_hsa_circ_312441,RMVar_hsa_circ_278308,RMVar_hsa_circ_74090,RMVar_hsa_circ_267896,RMVar_hsa_circ_12129,RMVar_hsa_circ_230353,RMVar_hsa_circ_230355,RMVar_hsa_circ_230356,RMVar_hsa_circ_230354 114580 RMVar_ID_114580 Human_SNP_ID_857231773 m1A Human chr5 - 180851244 180851239 180851244 CAAAGCCAAGAGTACAGCAAATATAAAGACAGAACAGGAAGGTGAGGCATCTGAGAAGAGCTTGC CAAAGCCAAGAGTACAGCAAATATAAAGACAG_____GAAGGTGAGGCATCTGAGAAGAGCTTGC CCTGTT C ZFP62 Ensembl:ENSG00000196670 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:180851194..180851425 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..37 33 STAD 1 - Human_RBP_ID_1660411,Human_RBP_ID_7425688,Human_RBP_ID_22300180,Human_RBP_ID_22527662,Human_RBP_ID_24548164 114581 RMVar_ID_114581 Human_SNP_ID_857263818 m1A Human chr5 + 179623096 179623096 179623096 CCGAGCAAGACCAGGGCAAGCCCCGGACCTTCACCACGAATCCCTCTCCACCTTCCGTGCCCAAC CCGAGCAAGACCAGGGCAAGCCCCGGACCTTCGCCACGAATCCCTCTCCACCTTCCGTGCCCAAC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:179622976..179623125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 12 large intestine 114582 RMVar_ID_114582 Human_SNP_ID_857285394 m1A Human chr5 + 134560797 134560797 134560797 GCTGACATTAGAGCGTGTGCTGGAGGAGCTGGAGACCCTGTGCCACCAGAATATGGCCAGGGCCA GCTGACATTAGAGCGTGTGCTGGAGGAGCTGGTGACCCTGTGCCACCAGAATATGGCCAGGGCCA A T JADE2 Ensembl:ENSG00000043143 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:134560701..134560838 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 4 lung Human_Splice_Rec_693050,Human_Splice_Rec_693076,Human_Splice_Rec_693094,Human_Splice_Rec_693114,Human_Splice_Rec_693134,Human_Splice_Rec_693142 RMVar_hsa_circ_29743,RMVar_hsa_circ_64432,RMVar_hsa_circ_89877,RMVar_hsa_circ_234507,RMVar_hsa_circ_313837,RMVar_hsa_circ_125756,RMVar_hsa_circ_1269,RMVar_hsa_circ_50840,RMVar_hsa_circ_7573,RMVar_hsa_circ_114599,RMVar_hsa_circ_83541,RMVar_hsa_circ_234510,RMVar_hsa_circ_374840,RMVar_hsa_circ_234511,RMVar_hsa_circ_124683,RMVar_hsa_circ_234514,RMVar_hsa_circ_80956,RMVar_hsa_circ_29663,RMVar_hsa_circ_234515,RMVar_hsa_circ_234512,RMVar_hsa_circ_234513,RMVar_hsa_circ_81818,RMVar_hsa_circ_234516 114583 RMVar_ID_114583 Human_SNP_ID_857371483 m1A Human chr5 + 154941133 154941133 154941133 AGGGCGAAAGATGGCGGCGGCAGTACTGGGACAGTTGGGTAAGGATTTCTTAGTGGTTAAGCGAC AGGGCGAAAGATGGCGGCGGCAGTACTGGGACTGTTGGGTAAGGATTTCTTAGTGGTTAAGCGAC A T MRPL22 Ensembl:ENSG00000082515 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:154941069..154950950;chr5:154941076..154950925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 5 bladder,urinary tract Human_RBP_ID_789157,Human_RBP_ID_5509143 Human_Splice_Rec_714031,Human_Splice_Rec_714043,Human_Splice_Rec_714063 114584 RMVar_ID_114584 Human_SNP_ID_857371579 m1A Human chr5 + 140679778 140679778 140679778 CAATCCATCCAAAGTCTCAAGAGCCCAAGTTTAGAAAGATACAGTGAGGTCATAGCGAAGGGACA CAATCCATCCAAAGTCTCAAGAGCCCAAGTTTGGAAAGATACAGTGAGGTCATAGCGAAGGGACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140679776..140679900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine 114585 RMVar_ID_114585 Human_SNP_ID_857372657 m1A Human chr5 - 103549232 103549232 103549232 AATAAAATTCGAGCTACATAAGTATATGGAAAATAATGTACCTTGATTATTATGAAATAGAGCAT AATAAAATTCGAGCTACATAAGTATATGGAAACTAATGTACCTTGATTATTATGAAATAGAGCAT T G NUDT12 Ensembl:ENSG00000112874 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10057908 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,ESCA 2 prostate GWAS_ID_7913,GWAS_ID_7914,GWAS_ID_7915,GWAS_ID_7916,GWAS_ID_7917 114586 RMVar_ID_114586 Human_SNP_ID_857380492 m1A Human chr5 + 420874 420871 420875 ACGCACAGACCCACGCACGCAGCCACCCACCCACGCAGCACGCACAGACCCACGCACGCAGCACG ACGCACAGACCCACGCACGCAGCCACCCAC____GCAGCACGCACAGACCCACGCACGCAGCACG CCCAC C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:420824..420922 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 LMS 1 - RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 114587 RMVar_ID_114587 Human_SNP_ID_857382007 m1A Human chr5 + 180292029 180292029 180292029 GCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACCCTTCCGGTCCCGCTCCCTTCTCCGCCGCTG GCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGCCCCTTCCGGTCCCGCTCCCTTCTCCGCCGCTG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:180291826..180292050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114588 RMVar_ID_114588 Human_SNP_ID_857385457 m1A Human chr5 + 160010641 160010641 160010641 GTGTGCTGGCCCTCCAGTTCCTGATCCCAAAAATCAGCATTCCCAGAGTAAGCTGCTCAGGGATG GTGTGCTGGCCCTCCAGTTCCTGATCCCAAAAGTCAGCATTCCCAGAGTAAGCTGCTCAGGGATG A G TTC1 Ensembl:ENSG00000113312 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:160010501..160010667 32194978 MeRIP-seq:(Medium) rs766245498 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_18837394 Human_miRNA_ID_2423705,Human_miRNA_ID_2433364,Human_miRNA_ID_2783625 RMVar_hsa_circ_105992,RMVar_hsa_circ_235898,RMVar_hsa_circ_104720,RMVar_hsa_circ_300823,RMVar_hsa_circ_343924,RMVar_hsa_circ_351422,RMVar_hsa_circ_309458,RMVar_hsa_circ_282804,RMVar_hsa_circ_235900,RMVar_hsa_circ_235902,RMVar_hsa_circ_235903,RMVar_hsa_circ_235901,RMVar_hsa_circ_235899 114589 RMVar_ID_114589 Human_SNP_ID_857391748 m1A Human chr5 - 397758 397757 397758 TGGTCAGGGGCTACGTGGACGGTCAGGGGCTAACATGGACGGTCAGGAGCTACGTGGACGGTCAG TGGTCAGGGGCTACGTGGACGGTCAGGGGCTA_CATGGACGGTCAGGAGCTACGTGGACGGTCAG GT G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:397626..398000 26863196 MeRIP-seq:(Medium) rs1376485097 Functional Loss DEL ICGC 33..33 33 PBCA 2 - 114590 RMVar_ID_114590 Human_SNP_ID_857428161 m1A Human chr5 - 150357739 150357739 150357739 CCCGCCGCTTCCTGGCCTCGGCCATACCCGCGACCCCCGGCCGGCCGGCTACCTGCACGCCCCGC CCCGCCGCTTCCTGGCCTCGGCCATACCCGCGCCCCCCGGCCGGCCGGCTACCTGCACGCCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:150357676..150357905;chr5:150357651..150364200;chr5:150357651..150357906 26863196 MeRIP-seq:(Medium) rs879085626 Functional Loss SNV ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 10 uterus 114591 RMVar_ID_114591 Human_SNP_ID_857446941 m1A Human chr5 - 31526235 31526235 31526235 AGAAAGGCTGAAACACTATGATGACCACAGGCACCGAGATCACAGTCATGGGCGAGGTGAGAGGC AGAAAGGCTGAAACACTATGATGACCACAGGCTCCGAGATCACAGTCATGGGCGAGGTGAGAGGC T A DROSHA Ensembl:ENSG00000113360 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:31526064..31526846 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_9306950,Human_RBP_ID_9397708,Human_RBP_ID_15422414,Human_RBP_ID_23050394,Human_RBP_ID_26350497,Human_RBP_ID_27515386 RMVar_hsa_circ_110996,RMVar_hsa_circ_230645 114592 RMVar_ID_114592 Human_SNP_ID_857466414 m1A Human chr5 + 181237038 181237037 181237039 CTCGCACCAGGTTGTCCGTGTAGCCAGCAAACAGAGTCTGCAGGGAAGAAATGACAGTGACAGGT CTCGCACCAGGTTGTCCGTGTAGCCAGCAAAC__AGTCTGCAGGGAAGAAATGACAGTGACAGGT CAG C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181237001..181237050 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..34 33 STAD,PBCA 2 - 114593 RMVar_ID_114593 Human_SNP_ID_857475315 m1A Human chr5 + 10239261 10239261 10239261 CAGGGTGCCACCCACAAGCCCAGTAAGTAAGAACCCCCAGTTGCTTTTCTGCAAACTGTTGACTT CAGGGTGCCACCCACAAGCCCAGTAAGTAAGAGCCCCCAGTTGCTTTTCTGCAAACTGTTGACTT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10239214..10239313 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA,SKCM 3 - 114594 RMVar_ID_114594 Human_SNP_ID_857484138 m1A Human chr5 - 119452607 119452607 119452607 GCTCACCTGCCCCCGCGCCGGTGACCAGTACCACCCGCCCGTCGAACCTCAGCGGTGAGCCCATG GCTCACCTGCCCCCGCGCCGGTGACCAGTACCGCCCGCCCGTCGAACCTCAGCGGTGAGCCCATG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:119452501..119452694;chr5:119452501..119452702 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114595 RMVar_ID_114595 Human_SNP_ID_857507555 m1A Human chr5 - 179801891 179801891 179801891 TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAAGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG TCGGTTGCACGCAGCTGAGCAGGAGAGCCTCAGGCGCTCCAAGGAGCTCAACCTGGTGCTGGACG T C MGAT4B Ensembl:ENSG00000161013 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs78450232 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_4826620,Human_RBP_ID_9307306,Human_RBP_ID_9398821,Human_RBP_ID_22099904 Human_Splice_Rec_730060,Human_Splice_Rec_730190,Human_Splice_Rec_730218,Human_Splice_Rec_730226,Human_Splice_Rec_730232,Human_Splice_Rec_730236,Human_Splice_Rec_730244 RMVar_hsa_circ_66113 114596 RMVar_ID_114596 Human_SNP_ID_857508826 m1A Human chr5 - 176975422 176975422 176975422 GAAAACGAAGACAAAACAGTCGAATAGAGCAAAGTGTTTGGCCAAAAGAAAAATCGCACGTATGT GAAAACGAAGACAAAACAGTCGAATAGAGCAACGTGTTTGGCCAAAAGAAAAATCGCACGTATGT T G UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176975354..176975421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_73964,Human_RBP_ID_944811,Human_RBP_ID_5610691,Human_RBP_ID_15393745,Human_RBP_ID_24098523,Human_RBP_ID_26352919,Human_RBP_ID_27826124 Human_Splice_Rec_723830,Human_Splice_Rec_723831,Human_Splice_Rec_723856,Human_Splice_Rec_723857,Human_Splice_Rec_723882,Human_Splice_Rec_723883,Human_Splice_Rec_723906,Human_Splice_Rec_723907,Human_Splice_Rec_723970,Human_Splice_Rec_723971,Human_Splice_Rec_723978,Human_Splice_Rec_723979,Human_Splice_Rec_723984,Human_Splice_Rec_723985,Human_Splice_Rec_723992,Human_Splice_Rec_723993,Human_Splice_Rec_723996 Human_miRNA_ID_879139,Human_miRNA_ID_1348605,Human_miRNA_ID_1812145 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_113131,RMVar_hsa_circ_3534,RMVar_hsa_circ_70873,RMVar_hsa_circ_236405,RMVar_hsa_circ_75709,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_328319,RMVar_hsa_circ_8543,RMVar_hsa_circ_311842,RMVar_hsa_circ_366032,RMVar_hsa_circ_288555,RMVar_hsa_circ_236416,RMVar_hsa_circ_64640,RMVar_hsa_circ_294228 114597 RMVar_ID_114597 Human_SNP_ID_857516238 m1A Human chr5 - 138467918 138467918 138467918 AGGAGTACGTGGTGGCCACCGACGGGGAGGGGAAGCCACTGTGCACAGGGGATGGGTAGGTCGAG AGGAGTACGTGGTGGCCACCGACGGGGAGGGGGAGCCACTGTGCACAGGGGATGGGTAGGTCGAG T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:138467870..138467971 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114598 RMVar_ID_114598 Human_SNP_ID_857516853 m1A Human chr5 + 181234019 181234019 181234019 AAGACCTGTCAGGTATCCTAGGAACAAGAGTGAGGAGCAAGATGAGCCTGCAGGAATCTGAGGCT AAGACCTGTCAGGTATCCTAGGAACAAGAGTGGGGAGCAAGATGAGCCTGCAGGAATCTGAGGCT A G TRIM41 Ensembl:ENSG00000146063 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:181234015..181234115 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 STAD 1 - RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 114599 RMVar_ID_114599 Human_SNP_ID_857519540 m1A Human chr5 - 150651553 150651553 150651553 CATCCCTTGGCCTCCTGCAGCAGCTCATTCCAACCCTTCCCTCACCAGGTCACCCTCACAGCCAT CATCCCTTGGCCTCCTGCAGCAGCTCATTCCAGCCCTTCCCTCACCAGGTCACCCTCACAGCCAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150651504..150651719 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114600 RMVar_ID_114600 Human_SNP_ID_857526372 m1A Human chr5 + 146459277 146459277 146459277 CACCTGCAGTATCCACTTCAACATCATCATCCACCCCTTCCTCTACCACTTCTACCACAACAACT CACCTGCAGTATCCACTTCAACATCATCATCCGCCCCTTCCTCTACCACTTCTACCACAACAACT A G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146459226..146459376 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_74821,Human_RBP_ID_249969,Human_RBP_ID_2906108,Human_RBP_ID_8267416,Human_RBP_ID_9399563,Human_RBP_ID_17298625,Human_RBP_ID_17412185,Human_RBP_ID_17528068,Human_RBP_ID_18041589,Human_RBP_ID_18538728,Human_RBP_ID_18956738,Human_RBP_ID_27512539,Human_RBP_ID_27825988 Human_Splice_Rec_705727,Human_Splice_Rec_705747,Human_Splice_Rec_705789,Human_Splice_Rec_705829,Human_Splice_Rec_705867 Human_miRNA_ID_2384056,Human_miRNA_ID_3094393 RMVar_hsa_circ_12950,RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300,RMVar_hsa_circ_306386,RMVar_hsa_circ_97072,RMVar_hsa_circ_108113,RMVar_hsa_circ_235303,RMVar_hsa_circ_373132,RMVar_hsa_circ_235304,RMVar_hsa_circ_235305,RMVar_hsa_circ_235306 114601 RMVar_ID_114601 Human_SNP_ID_857537203 m1A Human chr5 + 168494384 168494384 168494384 GGTTTCAGGAGAGTGGTGAAGGCTTGAAGTAGACGGTGAGACAGGAGCTTACAAGACAGCTTAAG GGTTTCAGGAGAGTGGTGAAGGCTTGAAGTAGGCGGTGAGACAGGAGCTTACAAGACAGCTTAAG A G RARS1 Ensembl:ENSG00000113643 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs13182927 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_1649540,Human_RBP_ID_7413053,Human_RBP_ID_15369560 RMVar_hsa_circ_29880,RMVar_hsa_circ_124053,RMVar_hsa_circ_289746,RMVar_hsa_circ_307071,RMVar_hsa_circ_333202,RMVar_hsa_circ_305517,RMVar_hsa_circ_270901,RMVar_hsa_circ_270821,RMVar_hsa_circ_236008,RMVar_hsa_circ_236010,RMVar_hsa_circ_236012,RMVar_hsa_circ_236013,RMVar_hsa_circ_236011,RMVar_hsa_circ_236009,RMVar_hsa_circ_236014,RMVar_hsa_circ_330181,RMVar_hsa_circ_336024,RMVar_hsa_circ_293764,RMVar_hsa_circ_349010,RMVar_hsa_circ_236015,RMVar_hsa_circ_236016,RMVar_hsa_circ_351023,RMVar_hsa_circ_319080,RMVar_hsa_circ_320336,RMVar_hsa_circ_314446,RMVar_hsa_circ_274915,RMVar_hsa_circ_275213,RMVar_hsa_circ_272045,RMVar_hsa_circ_236019,RMVar_hsa_circ_236021,RMVar_hsa_circ_236023,RMVar_hsa_circ_236024,RMVar_hsa_circ_236022,RMVar_hsa_circ_236020 114602 RMVar_ID_114602 Human_SNP_ID_857546049 m1A Human chr5 + 181260573 181260573 181260573 AGCATTCCCCCGATACAACACCTCTCGAATGGAGCCGTCCCATCCATCCATGGCCCCCACCGCTT AGCATTCCCCCGATACAACACCTCTCGAATGGTGCCGTCCCATCCATCCATGGCCCCCACCGCTT A T AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:181260345..181260753 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 114603 RMVar_ID_114603 Human_SNP_ID_857579020 m1A Human chr5 + 150080982 150080982 150080982 ATCGCAAGGTCACCGTTGCTCCTGGCTTCACGACCAGCTCAGGGACACTGGGCTCTATCACTGGG ATCGCAAGGTCACCGTTGCTCCTGGCTTCACGGCCAGCTCAGGGACACTGGGCTCTATCACTGGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150080935..150081079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine 114604 RMVar_ID_114604 Human_SNP_ID_857586979 m1A Human chr5 - 10748240 10748240 10748240 GTGAAAGCTGGTGGAATGCGAATTGTGCAGAAACACCCACATACAGGAGACACCAAAGAAGAGAA GTGAAAGCTGGTGGAATGCGAATTGTGCAGAAGCACCCACATACAGGAGACACCAAAGAAGAGAA T C DAP Ensembl:ENSG00000112977 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:10748201..10748275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_2879030,Human_RBP_ID_4845631,Human_RBP_ID_9397643 Human_Splice_Rec_635434,Human_Splice_Rec_635435,Human_Splice_Rec_635440,Human_Splice_Rec_635441,Human_Splice_Rec_635444,Human_Splice_Rec_635445,Human_Splice_Rec_635450,Human_Splice_Rec_635451,Human_Splice_Rec_635454,Human_Splice_Rec_635455,Human_Splice_Rec_635458 Human_miRNA_ID_2297070 RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 114605 RMVar_ID_114605 Human_SNP_ID_857627916 m1A Human chr5 + 641581 641581 641581 GCAGCCTCTGTTTAAACGCACGTGGCCCCCCCACCCCGCCTGGAAGCCTCTGCACGTGGCCTTCA GCAGCCTCTGTTTAAACGCACGTGGCCCCCCCCCCCCGCCTGGAAGCCTCTGCACGTGGCCTTCA A C CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:641545..641775 26863196 MeRIP-seq:(Medium) rs1257972552 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5326715,Human_RBP_ID_5531836,Human_RBP_ID_22099283 RMVar_hsa_circ_296269,RMVar_hsa_circ_310402,RMVar_hsa_circ_108129,RMVar_hsa_circ_60684,RMVar_hsa_circ_229964,RMVar_hsa_circ_229965,RMVar_hsa_circ_127958,RMVar_hsa_circ_340429,RMVar_hsa_circ_229971,RMVar_hsa_circ_229973,RMVar_hsa_circ_330905,RMVar_hsa_circ_229974,RMVar_hsa_circ_107416 114606 RMVar_ID_114606 Human_SNP_ID_857651439 m1A Human chr5 + 53560714 53560714 53560714 CAGTGGTACTGAGGCAGACGTTGTGGCGGAGAAGGGCAGTGGCTGTAGCTGCCCTTTCCGTTTCC CAGTGGTACTGAGGCAGACGTTGTGGCGGAGAGGGGCAGTGGCTGTAGCTGCCCTTTCCGTTTCC A G NDUFS4 Ensembl:ENSG00000164258 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr5:53560651..53573627;chr5:53560651..53560775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_643185,Human_RBP_ID_4833433,Human_RBP_ID_8617053,Human_RBP_ID_9399094,Human_RBP_ID_22460041 Human_Splice_Rec_650503,Human_Splice_Rec_650511,Human_Splice_Rec_650521,Human_Splice_Rec_650529,Human_Splice_Rec_650539 RMVar_hsa_circ_231352,RMVar_hsa_circ_80678,RMVar_hsa_circ_90741,RMVar_hsa_circ_231353 114607 RMVar_ID_114607 Human_SNP_ID_857666923 m1A Human chr5 + 14296140 14296139 14296140 AGAGGGGTTGTGTGGGAAGTGAGAGAAGGGGGAAAAACGTAGGGAAGTTTGGACAGATCAGGAAA AGAGGGGTTGTGTGGGAAGTGAGAGAAGGGGG_AAAACGTAGGGAAGTTTGGACAGATCAGGAAA GA G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:14295983..14296235 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_283,RMVar_hsa_circ_79613,RMVar_hsa_circ_230323,RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_291585,RMVar_hsa_circ_323713,RMVar_hsa_circ_341444,RMVar_hsa_circ_347025,RMVar_hsa_circ_344313,RMVar_hsa_circ_324581,RMVar_hsa_circ_315318,RMVar_hsa_circ_122686,RMVar_hsa_circ_230329,RMVar_hsa_circ_230331,RMVar_hsa_circ_230333,RMVar_hsa_circ_72119,RMVar_hsa_circ_230334,RMVar_hsa_circ_230332,RMVar_hsa_circ_230330,RMVar_hsa_circ_230327,RMVar_hsa_circ_230328,RMVar_hsa_circ_296611,RMVar_hsa_circ_64523,RMVar_hsa_circ_311291,RMVar_hsa_circ_372445,RMVar_hsa_circ_323300,RMVar_hsa_circ_300557,RMVar_hsa_circ_48236,RMVar_hsa_circ_230336,RMVar_hsa_circ_230337,RMVar_hsa_circ_230338,RMVar_hsa_circ_328078,RMVar_hsa_circ_230335,RMVar_hsa_circ_371911,RMVar_hsa_circ_298615,RMVar_hsa_circ_119805,RMVar_hsa_circ_288034,RMVar_hsa_circ_104964,RMVar_hsa_circ_51064,RMVar_hsa_circ_25150,RMVar_hsa_circ_6202,RMVar_hsa_circ_33778,RMVar_hsa_circ_230341,RMVar_hsa_circ_230343,RMVar_hsa_circ_230345,RMVar_hsa_circ_230346,RMVar_hsa_circ_230344,RMVar_hsa_circ_230342,RMVar_hsa_circ_230340,RMVar_hsa_circ_279668,RMVar_hsa_circ_290370,RMVar_hsa_circ_321654,RMVar_hsa_circ_322157,RMVar_hsa_circ_354676,RMVar_hsa_circ_297245,RMVar_hsa_circ_284160,RMVar_hsa_circ_48759,RMVar_hsa_circ_87690,RMVar_hsa_circ_42825,RMVar_hsa_circ_230348,RMVar_hsa_circ_5235,RMVar_hsa_circ_21682,RMVar_hsa_circ_230350,RMVar_hsa_circ_230351,RMVar_hsa_circ_230352,RMVar_hsa_circ_230349,RMVar_hsa_circ_276760,RMVar_hsa_circ_278990,RMVar_hsa_circ_323820,RMVar_hsa_circ_230347,RMVar_hsa_circ_312441,RMVar_hsa_circ_278308,RMVar_hsa_circ_74090,RMVar_hsa_circ_267896,RMVar_hsa_circ_12129,RMVar_hsa_circ_230353,RMVar_hsa_circ_230355,RMVar_hsa_circ_230356,RMVar_hsa_circ_230354 114608 RMVar_ID_114608 Human_SNP_ID_857681828 m1A Human chr5 - 127512151 127512151 127512151 GACCTGCACAGCCTTATGATCCCAGTTTTTACAATGAAACCTATGATTATGGTGGTTTTACAATG GACCTGCACAGCCTTATGATCCCAGTTTTTACGATGAAACCTATGATTATGGTGGTTTTACAATG T C HNRNPKP1 Ensembl:ENSG00000250859 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 114609 RMVar_ID_114609 Human_SNP_ID_857702713 m1A Human chr5 - 157294840 157294840 157294840 GGACAGTCTCACCTGGGGAATGGCCCGGGAACAGCTGCGCCAGGTGTACAGCATGACCGCATACT GGACAGTCTCACCTGGGGAATGGCCCGGGAACCGCTGCGCCAGGTGTACAGCATGACCGCATACT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:157294790..157294894 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 8 stomach 114610 RMVar_ID_114610 Human_SNP_ID_857729392 m1A Human chr5 + 177467482 177467482 177467482 CAGAGCCCACGGGTGCCAAACACACACTAACCACGGGCTCTGCGTTCTCATCCTCTCGCAGCCGC CAGAGCCCACGGGTGCCAAACACACACTAACCGCGGGCTCTGCGTTCTCATCCTCTCGCAGCCGC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177467472..177467650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 114611 RMVar_ID_114611 Human_SNP_ID_857752649 m1A Human chr5 + 179181091 179181091 179181091 ACAGTGCACTCACCTTTCCATAGCTCAGGAGGATGATCCGCACCAGGACCACGTTGATGTGGGCA ACAGTGCACTCACCTTTCCATAGCTCAGGAGGGTGATCCGCACCAGGACCACGTTGATGTGGGCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179152176..179181175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114612 RMVar_ID_114612 Human_SNP_ID_857773402 m1A Human chr5 + 168292131 168292131 168292131 AGCCCCCGCTGCGGCCGGGAGCTGCATGGGGGAGCGCCGGCAGCGCTTGGGAAGATGCCCCGGCC AGCCCCCGCTGCGGCCGGGAGCTGCATGGGGGGGCGCCGGCAGCGCTTGGGAAGATGCCCCGGCC A G WWC1 Ensembl:ENSG00000113645 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:168292081..168292204 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_74758 RMVar_hsa_circ_235991,RMVar_hsa_circ_103063,RMVar_hsa_circ_84612,RMVar_hsa_circ_235990 114613 RMVar_ID_114613 Human_SNP_ID_857786830 m1A Human chr5 - 160404546 160404546 160404546 GCATTTCAATCCTCCCTTTCAGCTGCATCAAGAAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA GCATTTCAATCCTCCCTTTCAGCTGCATCAAGTAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA T A SLU7 Ensembl:ENSG00000164609 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:160404401..160404575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_76531,Human_RBP_ID_214286,Human_RBP_ID_1660402,Human_RBP_ID_9349742,Human_RBP_ID_24548066,Human_RBP_ID_26351699,Human_RBP_ID_27826074 Human_Splice_Rec_716212 RMVar_hsa_circ_62418,RMVar_hsa_circ_124361,RMVar_hsa_circ_235923 114614 RMVar_ID_114614 Human_SNP_ID_857786832 m1A Human chr5 - 160404546 160404546 160404546 GCATTTCAATCCTCCCTTTCAGCTGCATCAAGAAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA GCATTTCAATCCTCCCTTTCAGCTGCATCAAGGAAAACTGAAAGAGGAAAAGAAGAAGAAGAAAA T C SLU7 Ensembl:ENSG00000164609 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:160404401..160404575 26863196 MeRIP-seq:(Medium) rs776637012 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach Human_RBP_ID_76531,Human_RBP_ID_214286,Human_RBP_ID_1660402,Human_RBP_ID_9349742,Human_RBP_ID_24548066,Human_RBP_ID_26351699,Human_RBP_ID_27826074 Human_Splice_Rec_716212 RMVar_hsa_circ_62418,RMVar_hsa_circ_124361,RMVar_hsa_circ_235923 114615 RMVar_ID_114615 Human_SNP_ID_857787218 m1A Human chr5 + 168414565 168414565 168414565 GGCTGGAAAAGGACCTGCAGGCAGCCCGGGACACCCAGAGCAAGGCGCTGACGGAGAGGTGGGGC GGCTGGAAAAGGACCTGCAGGCAGCCCGGGACGCCCAGAGCAAGGCGCTGACGGAGAGGTGGGGC A G WWC1 Ensembl:ENSG00000113645 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:168414404..168414600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_74794 Human_Splice_Rec_718343,Human_Splice_Rec_718387,Human_Splice_Rec_718445,Human_Splice_Rec_718487,Human_Splice_Rec_718495,Human_Splice_Rec_718527 Human_miRNA_ID_2423708,Human_miRNA_ID_2433367,Human_miRNA_ID_2906904,Human_miRNA_ID_3025736 RMVar_hsa_circ_368423,RMVar_hsa_circ_45853,RMVar_hsa_circ_30218,RMVar_hsa_circ_81451,RMVar_hsa_circ_235997,RMVar_hsa_circ_268954,RMVar_hsa_circ_235999,RMVar_hsa_circ_235998,RMVar_hsa_circ_54939,RMVar_hsa_circ_8838 114616 RMVar_ID_114616 Human_SNP_ID_857822699 m1A Human chr5 - 180795798 180795796 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCA__TTGCCTTGCTGATGTGCCAGCTGGGATTACG AAT A MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..34 33 SKCA 1 - Human_RBP_ID_9175517 Human_Splice_Rec_731658,Human_Splice_Rec_731678,Human_Splice_Rec_731688,Human_Splice_Rec_731690 RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 114617 RMVar_ID_114617 Human_SNP_ID_857826954 m1A Human chr5 - 417266 417266 417266 CACATATGGACCAAGCCGCCTTCTCCAGACTCAGGCCCTGCACATACAGACCAAGCCGCCTTCTC CACATATGGACCAAGCCGCCTTCTCCAGACTCGGGCCCTGCACATACAGACCAAGCCGCCTTCTC T C lnc-SLC9A3-4 RNACentral:URS00009C5F28 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:417256..417347 26863196 MeRIP-seq:(Medium) rs1408347080 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114618 RMVar_ID_114618 Human_SNP_ID_857846332 m1A Human chr5 - 892496 892496 892496 GGTCCTGGGCACCGGGCGAGGTCCTGGCCACGAGGGAGGGGTTCTGGGCACGCGGGAGGGGGTCC GGTCCTGGGCACCGGGCGAGGTCCTGGCCACGTGGGAGGGGTTCTGGGCACGCGGGAGGGGGTCC T A BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:892396..892721 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - Human_RBP_ID_4842899,Human_RBP_ID_9436836,Human_RBP_ID_18955830 Human_Splice_Rec_631959 114619 RMVar_ID_114619 Human_SNP_ID_857946152 m1A Human chr5 - 139614619 139614619 139614619 AACTGTTTATTCTGAAATTAATCTGAATACTTACTGGCCCCATTATTGTAGCTTGCCAATGGAAC AACTGTTTATTCTGAAATTAATCTGAATACTTGCTGGCCCCATTATTGTAGCTTGCCAATGGAAC T C RF00017-4685,RF00017-4497 RNACentral:URS0000985E23,RNACentral:URS000098F9B6 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139562332..139614915 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia 5 haematopoietic and lymphoid tissue 114620 RMVar_ID_114620 Human_SNP_ID_857954524 m1A Human chr5 + 69560295 69560295 69560295 CTGTGAGGCGCAGAGGTGGGGCAGGCCGTCTGACTAGCTAGGCGGCTGGGAGCGTTTTCGTGGCG CTGTGAGGCGCAGAGGTGGGGCAGGCCGTCTGGCTAGCTAGGCGGCTGGGAGCGTTTTCGTGGCG A G GTF2H2C Ensembl:ENSG00000183474 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:69560237..69560350;chr5:69560226..69560364 26863196 MeRIP-seq:(Medium) rs2666589 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4845764 114621 RMVar_ID_114621 Human_SNP_ID_857954811 m1A Human chr5 + 31526700 31526700 31526700 CTGACGGAGGCATGGGTGGGGGGAAGGGTACAAAGTCTGGTCGTGGAGGGAGAAAATTGGGGGCT CTGACGGAGGCATGGGTGGGGGGAAGGGTACACAGTCTGGTCGTGGAGGGAGAAAATTGGGGGCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:31526495..31526894 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 114622 RMVar_ID_114622 Human_SNP_ID_858017698 m1A Human chr5 + 176388915 176388914 176388916 GAGGGGCTGAGCCCCACTGTTTACAGGAATCCAGAGAGTTTCAAGGAAAAGTTCGTTCGCAAGAC GAGGGGCTGAGCCCCACTGTTTACAGGAATCC__AGAGTTTCAAGGAAAAGTTCGTTCGCAAGAC CAG C ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:176388751..176388993 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 LGG 1 - Human_RBP_ID_283999,Human_RBP_ID_638378,Human_RBP_ID_1650936,Human_RBP_ID_1992642,Human_RBP_ID_3967608,Human_RBP_ID_17415455,Human_RBP_ID_18195166,Human_RBP_ID_23214378 Human_Splice_Rec_723053 RMVar_hsa_circ_124328,RMVar_hsa_circ_125841,RMVar_hsa_circ_236366,RMVar_hsa_circ_236367 114623 RMVar_ID_114623 Human_SNP_ID_858083250 m1A Human chr5 + 1618806 1618806 1618806 TCCAGATGCACGGCCCTCAAACTGGAACATCAACTCCCCACCCAGGTCTCCAGCTCCACGGCCCT TCCAGATGCACGGCCCTCAAACTGGAACATCAGCTCCCCACCCAGGTCTCCAGCTCCACGGCCCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:1618642..1619032 26863196 MeRIP-seq:(Medium) rs1320716559 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114624 RMVar_ID_114624 Human_SNP_ID_858096587 m1A Human chr5 + 93587973 93587973 93587973 CAACCCAGCCCAATCCAGGCCAGTACGCACTCACCAACGGGGACCCCCTCAACGGCCACTGCTAC CAACCCAGCCCAATCCAGGCCAGTACGCACTCCCCAACGGGGACCCCCTCAACGGCCACTGCTAC A C NR2F1 Ensembl:ENSG00000175745 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:93587914..93588171 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_3781403,Human_RBP_ID_4857715,Human_RBP_ID_17415005,Human_RBP_ID_22100482 Human_Splice_Rec_673886,Human_Splice_Rec_673890,Human_Splice_Rec_673894,Human_Splice_Rec_673898,Human_Splice_Rec_673900 RMVar_hsa_circ_6452,RMVar_hsa_circ_233245 114625 RMVar_ID_114625 Human_SNP_ID_858109867 m1A Human chr5 + 79237118 79237118 79237118 GCCAAACCCATCCCGGGTCAGAAAACATCTGAAGCCGACGATGCGGCGGGGGCAGCCGCTGCAGC GCCAAACCCATCCCGGGTCAGAAAACATCTGAGGCCGACGATGCGGCGGGGGCAGCCGCTGCAGC A G JMY Ensembl:ENSG00000152409 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:79237069..79237338 26863196 MeRIP-seq:(Medium) rs1044484469 Functional Loss SNV TCGA 33..33 33 COAD 1 - 114626 RMVar_ID_114626 Human_SNP_ID_858140230 m1A Human chr5 + 172358858 172358858 172358858 CACGTTGCAGGGACCCAGCCTTGCTCCTCGGCAGTGCTGACGAACCACCAACCTGGGGAAGCAAG CACGTTGCAGGGACCCAGCCTTGCTCCTCGGCGGTGCTGACGAACCACCAACCTGGGGAAGCAAG A G RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172358808..172358873 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 114627 RMVar_ID_114627 Human_SNP_ID_858149227 m1A Human chr5 + 172007147 172007147 172007147 GTGGGTTCTAGGTGCGTTAGGAAGGTGTATAGACCTGGGGCTCAGGTGTGGGAAGGGGCCAGCGA GTGGGTTCTAGGTGCGTTAGGAAGGTGTATAGGCCTGGGGCTCAGGTGTGGGAAGGGGCCAGCGA A G lnc-EFCAB9-5,lnc-EFCAB9-5:2 RNACentral:URS0000D5BCA6,RNACentral:URS0000D5B06B lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:172007098..172007320 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114628 RMVar_ID_114628 Human_SNP_ID_858162214 m1A Human chr5 + 177371377 177371377 177371377 TGCAGGTGTGAAGATCTCCAAAGCCCGTGACAAATCTCCCTGCCGCAGCCAGGTGAGCGAAAGGC TGCAGGTGTGAAGATCTCCAAAGCCCGTGACACATCTCCCTGCCGCAGCCAGGTGAGCGAAAGGC A C RGS14 Ensembl:ENSG00000169220 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:177371368..177371469 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_944827,Human_RBP_ID_1212054 Human_Splice_Rec_724822,Human_Splice_Rec_724823,Human_Splice_Rec_724854,Human_Splice_Rec_724855,Human_Splice_Rec_724884,Human_Splice_Rec_724885,Human_Splice_Rec_724894,Human_Splice_Rec_724895,Human_Splice_Rec_724900,Human_Splice_Rec_724901,Human_Splice_Rec_724906,Human_Splice_Rec_724908,Human_Splice_Rec_724909,Human_Splice_Rec_724912,Human_Splice_Rec_724913 RMVar_hsa_circ_24416,RMVar_hsa_circ_126387,RMVar_hsa_circ_236486 114629 RMVar_ID_114629 Human_SNP_ID_858171997 m1A Human chr5 + 146289162 146289162 146289162 TGGAAAAAAAAAAGAAAAAAGATGAAAGTATTACAAATTTAAAAGAATTTGGAAAATTTATGAAC TGGAAAAAAAAAAGAAAAAAGATGAAAGTATTGCAAATTTAAAAGAATTTGGAAAATTTATGAAC A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs17687490 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22402657 GWAS_ID_15319,GWAS_ID_15320,GWAS_ID_15321,GWAS_ID_15322 RMVar_hsa_circ_121973,RMVar_hsa_circ_235261,RMVar_hsa_circ_267781,RMVar_hsa_circ_107671,RMVar_hsa_circ_235299 114630 RMVar_ID_114630 Human_SNP_ID_858176237 m1A Human chr5 + 77210648 77210648 77210648 GCGGGGAGCGTGTTTGGGGCGCCGCGGCGGGGAGGGTGGCGGCCGCTGGTGCGCGCGGGGCGCTG GCGGGGAGCGTGTTTGGGGCGCCGCGGCGGGGGGGGTGGCGGCCGCTGGTGCGCGCGGGGCGCTG A G AC022414.1,PDE8B Ensembl:ENSG00000284762,Ensembl:ENSG00000113231 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:77210520..77210771 26863196 MeRIP-seq:(Medium) rs1484977569 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114631 RMVar_ID_114631 Human_SNP_ID_858208547 m1A Human chr5 + 179724778 179724778 179724778 CAAGGGAGATGAGGAGGAGGAAGGAGAAGAGAAACTTGGTAAGAAACAGAGTCCAGAAAATCTGC CAAGGGAGATGAGGAGGAGGAAGGAGAAGAGATACTTGGTAAGAAACAGAGTCCAGAAAATCTGC A T CANX Ensembl:ENSG00000127022 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:179724776..179724800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_214300,Human_RBP_ID_787807,Human_RBP_ID_839485,Human_RBP_ID_944908,Human_RBP_ID_3968501,Human_RBP_ID_8236879,Human_RBP_ID_9306876,Human_RBP_ID_9398805,Human_RBP_ID_17662636,Human_RBP_ID_17671755,Human_RBP_ID_21215747,Human_RBP_ID_22772227,Human_RBP_ID_23050207,Human_RBP_ID_23116228,Human_RBP_ID_24100498,Human_RBP_ID_24548077,Human_RBP_ID_24554417,Human_RBP_ID_26351894,Human_RBP_ID_27826174 Human_Splice_Rec_729755,Human_Splice_Rec_729783,Human_Splice_Rec_729827,Human_Splice_Rec_729891,Human_Splice_Rec_729931 RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_97640,RMVar_hsa_circ_359776,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_236660,RMVar_hsa_circ_342219,RMVar_hsa_circ_236666,RMVar_hsa_circ_35863,RMVar_hsa_circ_358930,RMVar_hsa_circ_324650,RMVar_hsa_circ_236669 114632 RMVar_ID_114632 Human_SNP_ID_858212779 m1A Human chr5 + 157743845 157743845 157743845 CCCGCGGCTGGATGTCAGCTCTGACAGCTTCGACCCGCTGCTGGCCCTGTACGCGCCCCGCCTGC CCCGCGGCTGGATGTCAGCTCTGACAGCTTCGCCCCGCTGCTGGCCCTGTACGCGCCCCGCCTGC A C LSM11 Ensembl:ENSG00000155858 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:157743794..157743894 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1390788,Human_RBP_ID_1649014,Human_RBP_ID_8887352,Human_RBP_ID_27513375 Human_miRNA_ID_1487182 114633 RMVar_ID_114633 Human_SNP_ID_858233040 m1A Human chr5 + 140653009 140653007 140653009 TTATTATGCCAAGCTACGCCAACAAGAAATTGAGAGAGAGAGAGAGCTAGCAGAGAAGTACCGGG TTATTATGCCAAGCTACGCCAACAAGAAATT__GAGAGAGAGAGAGCTAGCAGAGAAGTACCGGG TGA T IK Ensembl:ENSG00000113141 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:140652129..140653150 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 ESCA 1 - Human_RBP_ID_5532070,Human_RBP_ID_9398368,Human_RBP_ID_22100709,Human_RBP_ID_24548134,Human_RBP_ID_26351439,Human_RBP_ID_27825918 Human_Splice_Rec_700378,Human_Splice_Rec_700386,Human_Splice_Rec_700394,Human_Splice_Rec_700430,Human_Splice_Rec_700438,Human_Splice_Rec_700454,Human_Splice_Rec_700462 RMVar_hsa_circ_362849 114634 RMVar_ID_114634 Human_SNP_ID_858242230 m1A Human chr5 + 72196430 72196430 72196430 CAATCTGAAGAGGAGGCTGATGAGGAGGACAAAGCTGAAGATGCCAGAGAGGAGGAATATGAGCC CAATCTGAAGAGGAGGCTGATGAGGAGGACAACGCTGAAGATGCCAGAGAGGAGGAATATGAGCC A C MAP1B Ensembl:ENSG00000131711 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:72196258..72196461 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_RBP_ID_214147,Human_RBP_ID_1660368,Human_RBP_ID_7465306,Human_RBP_ID_8891809,Human_RBP_ID_9262245,Human_RBP_ID_9306485,Human_RBP_ID_9397888,Human_RBP_ID_18413674,Human_RBP_ID_22099451,Human_RBP_ID_23116248,Human_RBP_ID_24548190,Human_RBP_ID_26350939,Human_RBP_ID_27574133,Human_RBP_ID_27825490 Human_miRNA_ID_957430,Human_miRNA_ID_2254367 RMVar_hsa_circ_94751,RMVar_hsa_circ_8171,RMVar_hsa_circ_232270,RMVar_hsa_circ_232277 114635 RMVar_ID_114635 Human_SNP_ID_858374816 m1A Human chr5 - 1461558 1461558 1461558 ACGCAGCGGGCCCCTGGTGGCCTGGGGGCCAGACCCGTGGGCAGGTGGGGCATGGGCCCTGGCCT ACGCAGCGGGCCCCTGGTGGCCTGGGGGCCAGGCCCGTGGGCAGGTGGGGCATGGGCCCTGGCCT T C LPCAT1 Ensembl:ENSG00000153395 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1461508..1461611 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_634476,Human_RBP_ID_5121623,Human_RBP_ID_5151069 Human_miRNA_ID_474995 114636 RMVar_ID_114636 Human_SNP_ID_858379727 m1A Human chr5 + 172689966 172689966 172689966 TCTCTTGTTATTCAGGGGTGTCCACAGTTAGGAAGGGACCTGGGGCCTTGTCCCACCACCTTCCT TCTCTTGTTATTCAGGGGTGTCCACAGTTAGGGAGGGACCTGGGGCCTTGTCCCACCACCTTCCT A G NEURL1B Ensembl:ENSG00000214357 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3205179 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver GWAS_ID_7685,GWAS_ID_7686 114637 RMVar_ID_114637 Human_SNP_ID_858388898 m1A Human chr5 + 151803950 151803950 151803950 GTCGAAGAGAAGAAGACTCGAGCTGCCAGGGAAGGCGACCGACGAGATAATCGCCTTCGGGGACC GTCGAAGAGAAGAAGACTCGAGCTGCCAGGGAGGGCGACCGACGAGATAATCGCCTTCGGGGACC A G G3BP1 Ensembl:ENSG00000145907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:151803901..151804080 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus Human_RBP_ID_250189,Human_RBP_ID_635596,Human_RBP_ID_946780,Human_RBP_ID_1648519,Human_RBP_ID_1990731,Human_RBP_ID_7407036,Human_RBP_ID_8893808,Human_RBP_ID_9398589,Human_RBP_ID_15355695,Human_RBP_ID_22460282,Human_RBP_ID_23116281,Human_RBP_ID_24548150 Human_Splice_Rec_712530,Human_Splice_Rec_712552,Human_Splice_Rec_712606,Human_Splice_Rec_712628 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235631,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 114638 RMVar_ID_114638 Human_SNP_ID_858390899 m1A Human chr5 - 154872613 154872613 154872613 CATCCTAAAGAAAGCCATTCCTGTCAGCAGTGAGTCTGAGCCTGCCTGGTGCTGCCTTCCAATCC CATCCTAAAGAAAGCCATTCCTGTCAGCAGTGCGTCTGAGCCTGCCTGGTGCTGCCTTCCAATCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154871847..154872613 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 114639 RMVar_ID_114639 Human_SNP_ID_858405793 m1A Human chr5 + 150555066 150555066 150555066 AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCATGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA AGAAAGGGGAGGTGGCCTGCTTGGCCGACGTCGTGGAGCCAGCTGGGAGCAGGGCTGAGCGTTGA A G NDST1 Ensembl:ENSG00000070614 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150555015..150555140 26863196 MeRIP-seq:(Medium) rs143181608 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_4851580,Human_RBP_ID_26529409 Human_miRNA_ID_266587,Human_miRNA_ID_2082783,Human_miRNA_ID_2380364,Human_miRNA_ID_3023377 RMVar_hsa_circ_89710,RMVar_hsa_circ_235476 114640 RMVar_ID_114640 Human_SNP_ID_858407556 m1A Human chr5 + 41762139 41762139 41762139 TTACCTTTGCAGAATGCTCCATGGTGACCACCACTTTGGTTTTCGCACTGGACACTAAATCCATA TTACCTTTGCAGAATGCTCCATGGTGACCACCCCTTTGGTTTTCGCACTGGACACTAAATCCATA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:41749585..41794040 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 4 skin,head and neck 114641 RMVar_ID_114641 Human_SNP_ID_858410961 m1A Human chr5 + 34192281 34192281 34192281 TGAGGACGGACCTCAGGCTGTCTCTTCGCGTCACACCCGCTGTGAAAAGGCAGATACAGCACCAG TGAGGACGGACCTCAGGCTGTCTCTTCGCGTCGCACCCGCTGTGAAAAGGCAGATACAGCACCAG A G AC138409.1 Ensembl:ENSG00000215156 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:34192103..34192404 32194978 MeRIP-seq:(Medium) rs1391442931 Functional Loss SNV TCGA 33..33 33 UCEC 1 - 114642 RMVar_ID_114642 Human_SNP_ID_858421891 m1A Human chr5 - 93683461 93683461 93683461 CTGGCAACTTTGAAAATGTCTGTACAGCCAACAGTTTCCCTTGGGGGCTTTGAAATAACACCACC CTGGCAACTTTGAAAATGTCTGTACAGCCAACGGTTTCCCTTGGGGGCTTTGAAATAACACCACC T C NPM1P27,FAM172A Ensembl:ENSG00000249353,Ensembl:ENSG00000113391 Pseudogene,Protein coding exon,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs538281040 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast 114643 RMVar_ID_114643 Human_SNP_ID_858454420 m1A Human chr5 - 132761195 132761195 132761195 TAAGTGAGCTGCAGAGGAAGGAGGAAGAGATGAGGCAGATGTTTGTCAACAAAGTGAAGGAGACA TAAGTGAGCTGCAGAGGAAGGAGGAAGAGATGGGGCAGATGTTTGTCAACAAAGTGAAGGAGACA T C SEPTIN8 Ensembl:ENSG00000164402 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:132761126..132761275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus Human_RBP_ID_12732,Human_RBP_ID_3967382,Human_RBP_ID_7381792,Human_RBP_ID_26351227,Human_RBP_ID_27825747 Human_Splice_Rec_691584,Human_Splice_Rec_691585,Human_Splice_Rec_691602,Human_Splice_Rec_691603,Human_Splice_Rec_691618,Human_Splice_Rec_691619,Human_Splice_Rec_691638,Human_Splice_Rec_691639,Human_Splice_Rec_691654,Human_Splice_Rec_691655,Human_Splice_Rec_691670,Human_Splice_Rec_691671,Human_Splice_Rec_691688,Human_Splice_Rec_691689,Human_Splice_Rec_691704,Human_Splice_Rec_691705,Human_Splice_Rec_691720,Human_Splice_Rec_691721 RMVar_hsa_circ_11562,RMVar_hsa_circ_88096,RMVar_hsa_circ_110676,RMVar_hsa_circ_91808,RMVar_hsa_circ_234380,RMVar_hsa_circ_234382,RMVar_hsa_circ_78190,RMVar_hsa_circ_234381,RMVar_hsa_circ_52964,RMVar_hsa_circ_234379,RMVar_hsa_circ_48517 114644 RMVar_ID_114644 Human_SNP_ID_858461193 m1A Human chr5 - 90525273 90525273 90525273 TCCAGATTTTAACATTATGGCAGGGAGGCATCAGAATCGTAGTTTTCCTCTTCCAGGAGTTCAGT TCCAGATTTTAACATTATGGCAGGGAGGCATCGGAATCGTAGTTTTCCTCTTCCAGGAGTTCAGT T C LYSMD3 Ensembl:ENSG00000176018 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:90525222..90525336 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_18055502 Human_Splice_Rec_671670,Human_Splice_Rec_671674,Human_Splice_Rec_671678,Human_Splice_Rec_671682 RMVar_hsa_circ_73902,RMVar_hsa_circ_233102,RMVar_hsa_circ_78834,RMVar_hsa_circ_233103,RMVar_hsa_circ_62019 114645 RMVar_ID_114645 Human_SNP_ID_858462248 m1A Human chr5 + 157743811 157743811 157743811 CGGCTGGCGCCGGGAGCCCCGCGCGCCCGCCCAGCCCGCGGCTGGATGTCAGCTCTGACAGCTTC CGGCTGGCGCCGGGAGCCCCGCGCGCCCGCCCCGCCCGCGGCTGGATGTCAGCTCTGACAGCTTC A C LSM11 Ensembl:ENSG00000155858 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:157743763..157743885 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 114646 RMVar_ID_114646 Human_SNP_ID_858496689 m1A Human chr5 - 98856032 98856032 98856032 TCAGTGATTTTAGACTGACCTCCATTTAAATTATGTTTATATATGAACTTTACTCTGACCTGTGA TCAGTGATTTTAGACTGACCTCCATTTAAATTGTGTTTATATATGAACTTTACTCTGACCTGTGA T C CHD1 Ensembl:ENSG00000153922 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2455425 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2954742,Human_RBP_ID_8625750,Human_RBP_ID_23052547,Human_RBP_ID_24508979,Human_RBP_ID_25931461,Human_RBP_ID_26531240 GWAS_ID_7905,GWAS_ID_7906,GWAS_ID_7907,GWAS_ID_7908,GWAS_ID_7909,GWAS_ID_7910,GWAS_ID_7911,GWAS_ID_7912 114647 RMVar_ID_114647 Human_SNP_ID_858561881 m1A Human chr5 + 55307860 55307858 55307861 TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGG___AAAAAAAAAAGTCAGGGGAACATTTTTGTCG GAAA G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55307809..55307959 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 COAD,UCEC 2 - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 114648 RMVar_ID_114648 Human_SNP_ID_858591962 m1A Human chr5 + 109409887 109409887 109409887 GGCTCCGGAGCGAGAACAGCGCTCGAACCTCCACCCGCCACCACCGCCTTCTTCTCCGCCTCCAA GGCTCCGGAGCGAGAACAGCGCTCGAACCTCCCCCCGCCACCACCGCCTTCTTCTCCGCCTCCAA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:109409797..109409905;chr5:109409799..109409901;chr5:109409802..109409903 26863196 MeRIP-seq:(Medium) rs900469488 Functional Loss SNV ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 2 uterus 114649 RMVar_ID_114649 Human_SNP_ID_858617602 m1A Human chr5 + 25910576 25910576 25910576 TGGGGAGGCTGAAGCAGATCGAGGAACAGACTAAGAAGGCTCAGCAAGAACTGGAAGAACAGACC TGGGGAGGCTGAAGCAGATCGAGGAACAGACTTAGAAGGCTCAGCAAGAACTGGAAGAACAGACC A T MSNP1 Ensembl:ENSG00000251593 Pseudogene exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:25910513..25910598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_4828380,Human_RBP_ID_5610786,Human_RBP_ID_8267934,Human_RBP_ID_17416567,Human_RBP_ID_18538442 114650 RMVar_ID_114650 Human_SNP_ID_858621416 m1A Human chr5 - 43602969 43602969 43602969 CAGGGGCCCTTCCACTCTCGGGGACAGGCGAAACCTCTTTGTCTCTGCCTCGGCCTGCGGCCCCC CAGGGGCCCTTCCACTCTCGGGGACAGGCGAACCCTCTTTGTCTCTGCCTCGGCCTGCGGCCCCC T G NNT-AS1 Ensembl:ENSG00000248092 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:43602919..43603983 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3784899,Human_RBP_ID_4846379 114651 RMVar_ID_114651 Human_SNP_ID_858624351 m1A Human chr5 + 71510765 71510765 71510765 CAGAGGAGGTCAAGCCTGTAGGTAAAATGGAGACAGATTTGAAAGAAATTAGAGAAGAAATTTCC CAGAGGAGGTCAAGCCTGTAGGTAAAATGGAGGCAGATTTGAAAGAAATTAGAGAAGAAATTTCC A G BDP1 Ensembl:ENSG00000145734 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:71510578..71510884 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8891652,Human_RBP_ID_18846337,Human_RBP_ID_24114446 Human_miRNA_ID_2046954 RMVar_hsa_circ_746,RMVar_hsa_circ_99788,RMVar_hsa_circ_267624,RMVar_hsa_circ_92883,RMVar_hsa_circ_266589,RMVar_hsa_circ_232195,RMVar_hsa_circ_68577,RMVar_hsa_circ_116406,RMVar_hsa_circ_24808,RMVar_hsa_circ_232198,RMVar_hsa_circ_127599,RMVar_hsa_circ_232200,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232206,RMVar_hsa_circ_232201,RMVar_hsa_circ_232202,RMVar_hsa_circ_344419,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_267014,RMVar_hsa_circ_232207,RMVar_hsa_circ_232204,RMVar_hsa_circ_232205,RMVar_hsa_circ_306242,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_30537,RMVar_hsa_circ_232213,RMVar_hsa_circ_232209,RMVar_hsa_circ_232211,RMVar_hsa_circ_232212,RMVar_hsa_circ_232210,RMVar_hsa_circ_363518,RMVar_hsa_circ_337416,RMVar_hsa_circ_356163,RMVar_hsa_circ_283938,RMVar_hsa_circ_232215,RMVar_hsa_circ_232217,RMVar_hsa_circ_232216,RMVar_hsa_circ_232214,RMVar_hsa_circ_232225,RMVar_hsa_circ_232221,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_120896,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232220,RMVar_hsa_circ_270747,RMVar_hsa_circ_332213,RMVar_hsa_circ_69265,RMVar_hsa_circ_232224 114652 RMVar_ID_114652 Human_SNP_ID_858672152 m1A Human chr5 - 150701010 150701010 150701010 TTGTGGCGGTCCTCTCTCCCAATTCGGAAGCTACAGCTACCTCCGGACGCTCTCAAGATGGCGAC TTGTGGCGGTCCTCTCTCCCAATTCGGAAGCTGCAGCTACCTCCGGACGCTCTCAAGATGGCGAC T C RBM22 Ensembl:ENSG00000086589 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:150700893..150701009 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1648372,Human_RBP_ID_9172729,Human_RBP_ID_24091124 Human_Splice_Rec_710867,Human_Splice_Rec_710891,Human_Splice_Rec_710905,Human_Splice_Rec_710915,Human_Splice_Rec_710925 114653 RMVar_ID_114653 Human_SNP_ID_858688746 m1A Human chr5 - 154598195 154598195 154598195 CATCCATCCACCCATCTATCCAGCCATCATCCATCCATTCATCCATCCATCCACTCACCTCTTCA CATCCATCCACCCATCTATCCAGCCATCATCCGTCCATTCATCCATCCATCCACTCACCTCTTCA T C RF00017-4483,RF00017-4490 RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:154598184..154598317 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114654 RMVar_ID_114654 Human_SNP_ID_858693146 m1A Human chr5 - 6749557 6749557 6749557 TCCTGAGTTACTTTGATGATTCTTCCTAAAGTACTGCAAAGGGACATTGTTGGAGATCAACAGAG TCCTGAGTTACTTTGATGATTCTTCCTAAAGTGCTGCAAAGGGACATTGTTGGAGATCAACAGAG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:6749551..6749600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114655 RMVar_ID_114655 Human_SNP_ID_858716489 m1A Human chr5 + 197797 197797 197797 TCTCTCTTTTCCCTACACCGCTGCCCCGTATCACCCCCTCCCGGAGTGTGTCCCCACCCCAGTGG TCTCTCTTTTCCCTACACCGCTGCCCCGTATCCCCCCCTCCCGGAGTGTGTCCCCACCCCAGTGG A C RF00017-2064,RF00017-1033 RNACentral:URS000098196C,RNACentral:URS0000984FD7 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:197747..197907 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114656 RMVar_ID_114656 Human_SNP_ID_858723772 m1A Human chr5 - 53560702 53560702 53560702 GGCAGCTACAGCCACTGCCCTTCTCCGCCACAACGTCTGCCTCAGTACCACTGACATTGACACCG GGCAGCTACAGCCACTGCCCTTCTCCGCCACAGCGTCTGCCTCAGTACCACTGACATTGACACCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:53560651..53560775;chr5:53560651..53560796 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_18843540 114657 RMVar_ID_114657 Human_SNP_ID_858727856 m1A Human chr5 - 179132899 179132899 179132899 CTCAAGTGCTCACTGCCTCCTCCCCCAACAGAAGGTGGGCTGTGACGGTGTGATCGGCTCCAGCA CTCAAGTGCTCACTGCCTCCTCCCCCAACAGACGGTGGGCTGTGACGGTGTGATCGGCTCCAGCA T G ADAMTS2 Ensembl:ENSG00000087116 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179132856..179137890 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_Splice_Rec_728862,Human_Splice_Rec_728910 RMVar_hsa_circ_36669,RMVar_hsa_circ_275328,RMVar_hsa_circ_45784,RMVar_hsa_circ_14901,RMVar_hsa_circ_31517 114658 RMVar_ID_114658 Human_SNP_ID_858772865 m1A Human chr5 - 172932482 172932482 172932482 TAGGAGTACCGCTGCTTGCCACTCTTGTCCTCATAAACCGTGGGCACAATCTTCAGGATGTAGTC TAGGAGTACCGCTGCTTGCCACTCTTGTCCTCCTAAACCGTGGGCACAATCTTCAGGATGTAGTC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:172932426..172932550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 114659 RMVar_ID_114659 Human_SNP_ID_858775374 m1A Human chr5 - 150444504 150444504 150444504 TCAGGAAATTCGAGGAACTGGCAGATGGGGCCACTTCATGTTCACATCCATCTGTTAGGTACTGG TCAGGAAATTCGAGGAACTGGCAGATGGGGCCGCTTCATGTTCACATCCATCTGTTAGGTACTGG T C RPS14 Ensembl:ENSG00000164587 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2073472 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_8607557,Human_RBP_ID_15351867 Human_Splice_Rec_710707 RMVar_hsa_circ_126237,RMVar_hsa_circ_89631,RMVar_hsa_circ_105764,RMVar_hsa_circ_83093,RMVar_hsa_circ_235464,RMVar_hsa_circ_235466,RMVar_hsa_circ_235465,RMVar_hsa_circ_235463 114660 RMVar_ID_114660 Human_SNP_ID_858781285 m1A Human chr5 - 176347698 176347698 176347698 TGGCTGAAGATCCAGCAGCCTTGAAGCCCCCCAAGATGGACATCCCAGTGATGGAAGGAAAGAAA TGGCTGAAGATCCAGCAGCCTTGAAGCCCCCCGAGATGGACATCCCAGTGATGGAAGGAAAGAAA T C KIAA1191 Ensembl:ENSG00000122203 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176347652..176347755 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_74969,Human_RBP_ID_638248,Human_RBP_ID_1650905,Human_RBP_ID_3968421,Human_RBP_ID_4852984,Human_RBP_ID_9174813,Human_RBP_ID_9398690,Human_RBP_ID_27334489,Human_RBP_ID_27514083 RMVar_hsa_circ_113477,RMVar_hsa_circ_236354,RMVar_hsa_circ_89766,RMVar_hsa_circ_236353 114661 RMVar_ID_114661 Human_SNP_ID_858844310 m1A Human chr5 - 177961336 177961336 177961336 CACGCTCCCTCTTCAGTGTCACCACGGCCATCATTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC CACGCTCCCTCTTCAGTGTCACCACGGCCATCGTTCCCTCTGCCAGCTCCTTCCTCAATGTCAGC T C RF00017-4673,lnc-PROP1-2,lnc-PROP1-2:2,RF00017-4525 RNACentral:URS000091B0E9,RNACentral:URS00008C2710,RNACentral:URS00008C153C,RNACentral:URS00009368C0 SRP RNA,lincRNA,lincRNA,SRP RNA intron,intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177961248..177961465 26863196 MeRIP-seq:(Medium) rs10040126 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 114662 RMVar_ID_114662 Human_SNP_ID_858875446 m1A Human chr5 + 138574029 138574029 138574029 CACAAATGTAGAAAACACTGCTTTGAAGTTTAATATGTATTCCCTCTCAAAGGAAATGATATTAT CACAAATGTAGAAAACACTGCTTTGAAGTTTAGTATGTATTCCCTCTCAAAGGAAATGATATTAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138574027..138574172 26863196 MeRIP-seq:(Medium) rs1442089315 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114663 RMVar_ID_114663 Human_SNP_ID_858879066 m1A Human chr5 + 177882471 177882471 177882471 CCCATGGGGAAGTACTTTGCCACAGGAAGTGCAGATGCTTTGGTCAGCCTCTGGGATGTGGATGA CCCATGGGGAAGTACTTTGCCACAGGAAGTGCGGATGCTTTGGTCAGCCTCTGGGATGTGGATGA A G AC106795.1 Ensembl:ENSG00000170089 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11552883 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_17415848 Human_Splice_Rec_726711,Human_Splice_Rec_726737,Human_Splice_Rec_726747,Human_Splice_Rec_726763,Human_Splice_Rec_726769,Human_Splice_Rec_726773,Human_Splice_Rec_726777,Human_Splice_Rec_726779 Human_miRNA_ID_1858155,Human_miRNA_ID_1880932,Human_miRNA_ID_1906932,Human_miRNA_ID_2430591,Human_miRNA_ID_2713339,Human_miRNA_ID_3049319 RMVar_hsa_circ_39670,RMVar_hsa_circ_116902,RMVar_hsa_circ_236558,RMVar_hsa_circ_44962,RMVar_hsa_circ_47623 114664 RMVar_ID_114664 Human_SNP_ID_858933723 m1A Human chr5 + 176389423 176389423 176389423 GCCAGCGCTCTCAGCTCATGATGCGCACCCGGATCGCCGCCCAGGGTTTCACGGTCGCAGCCATC GCCAGCGCTCTCAGCTCATGATGCGCACCCGGGTCGCCGCCCAGGGTTTCACGGTCGCAGCCATC A G ARL10,HIGD2A Ensembl:ENSG00000175414,Ensembl:ENSG00000146066 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176389292..176389518 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_638386,Human_RBP_ID_1650943,Human_RBP_ID_17415456,Human_RBP_ID_24098110 Human_Splice_Rec_723054 RMVar_hsa_circ_125841,RMVar_hsa_circ_236367,RMVar_hsa_circ_75961,RMVar_hsa_circ_236368 114665 RMVar_ID_114665 Human_SNP_ID_858934436 m1A Human chr5 - 138573837 138573837 138573837 TGTTCTAAATGTCTTACAGATCAGAAGCAATCAAGGGAGCAGTTGTTGGTATTGATTTGGGTACT TGTTCTAAATGTCTTACAGATCAGAAGCAATCGAGGGAGCAGTTGTTGGTATTGATTTGGGTACT T C HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138573708..138573901 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_74199,Human_RBP_ID_632771,Human_RBP_ID_943007,Human_RBP_ID_1210831,Human_RBP_ID_1987878,Human_RBP_ID_3968211,Human_RBP_ID_4850139,Human_RBP_ID_5395714,Human_RBP_ID_7390324,Human_RBP_ID_9335727,Human_RBP_ID_9349697,Human_RBP_ID_17302363,Human_RBP_ID_18039779,Human_RBP_ID_18448142,Human_RBP_ID_22460208,Human_RBP_ID_22680763,Human_RBP_ID_24386562,Human_RBP_ID_27735380 Human_Splice_Rec_696712,Human_Splice_Rec_696713,Human_Splice_Rec_696744,Human_Splice_Rec_696745,Human_Splice_Rec_696792,Human_Splice_Rec_696793,Human_Splice_Rec_696826,Human_Splice_Rec_696827,Human_Splice_Rec_696840,Human_Splice_Rec_696841,Human_Splice_Rec_696846,Human_Splice_Rec_696847,Human_Splice_Rec_696854,Human_Splice_Rec_696855,Human_Splice_Rec_696862,Human_Splice_Rec_696863,Human_Splice_Rec_696868,Human_Splice_Rec_696869 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_234835,RMVar_hsa_circ_370666,RMVar_hsa_circ_234838,RMVar_hsa_circ_54836,RMVar_hsa_circ_354397,RMVar_hsa_circ_234847,RMVar_hsa_circ_80971,RMVar_hsa_circ_35334,RMVar_hsa_circ_346812,RMVar_hsa_circ_359269,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_234855,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234854,RMVar_hsa_circ_41346,RMVar_hsa_circ_341181 114666 RMVar_ID_114666 Human_SNP_ID_858936673 m1A Human chr5 + 139325504 139325503 139325504 CGAAGCAGCGTTGGAAAATGGAATTAAAAATGAGGAAAACACAGAACCAGGTGCTGAATCTTCTG CGAAGCAGCGTTGGAAAATGGAATTAAAAATG_GGAAAACACAGAACCAGGTGCTGAATCTTCTG GA G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:139325453..139325587 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 CESC 1 - Human_RBP_ID_73090,Human_RBP_ID_284414,Human_RBP_ID_1210922,Human_RBP_ID_1645980,Human_RBP_ID_1988238,Human_RBP_ID_2956831,Human_RBP_ID_3759434,Human_RBP_ID_7392241,Human_RBP_ID_8267376,Human_RBP_ID_8604437,Human_RBP_ID_8885089,Human_RBP_ID_9170452,Human_RBP_ID_9398316,Human_RBP_ID_15320318,Human_RBP_ID_17298275,Human_RBP_ID_17411844,Human_RBP_ID_17527643,Human_RBP_ID_18183076,Human_RBP_ID_18413715,Human_RBP_ID_18537766,Human_RBP_ID_18833835,Human_RBP_ID_19124738,Human_RBP_ID_24085906,Human_RBP_ID_24548023,Human_RBP_ID_26351389,Human_RBP_ID_27074845,Human_RBP_ID_27735508,Human_RBP_ID_27826838 Human_Splice_Rec_697500,Human_Splice_Rec_697552,Human_Splice_Rec_697588,Human_Splice_Rec_697832,Human_Splice_Rec_697860,Human_Splice_Rec_697892,Human_Splice_Rec_697938,Human_Splice_Rec_697966,Human_Splice_Rec_698044 Human_miRNA_ID_2998039 RMVar_hsa_circ_234897,RMVar_hsa_circ_101392,RMVar_hsa_circ_85144,RMVar_hsa_circ_56035,RMVar_hsa_circ_234896,RMVar_hsa_circ_62131,RMVar_hsa_circ_234919,RMVar_hsa_circ_72323,RMVar_hsa_circ_288584,RMVar_hsa_circ_61079,RMVar_hsa_circ_33277,RMVar_hsa_circ_320086,RMVar_hsa_circ_68813,RMVar_hsa_circ_350313 114667 RMVar_ID_114667 Human_SNP_ID_858942339 m1A Human chr5 - 138559977 138559977 138559977 CCATTCAGGGAGGTGTGTTGGCCGGCGATGTCACGGATGTGCTGCTCCTTGATGTCACTCCCCTG CCATTCAGGGAGGTGTGTTGGCCGGCGATGTCGCGGATGTGCTGCTCCTTGATGTCACTCCCCTG T C HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138559927..138560004 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_249892,Human_RBP_ID_787548,Human_RBP_ID_1987844,Human_RBP_ID_3967436,Human_RBP_ID_4850107,Human_RBP_ID_7390203,Human_RBP_ID_8884918,Human_RBP_ID_9262292,Human_RBP_ID_9306624,Human_RBP_ID_9398275,Human_RBP_ID_17707090,Human_RBP_ID_18056889,Human_RBP_ID_22100693,Human_RBP_ID_22458940,Human_RBP_ID_24085309,Human_RBP_ID_27074609,Human_RBP_ID_27826825 Human_miRNA_ID_2098946,Human_miRNA_ID_2104895,Human_miRNA_ID_2110846,Human_miRNA_ID_2163392,Human_miRNA_ID_2594611,Human_miRNA_ID_2721554,Human_miRNA_ID_2737558,Human_miRNA_ID_2902296,Human_miRNA_ID_3038155 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_26156,RMVar_hsa_circ_70390,RMVar_hsa_circ_272810,RMVar_hsa_circ_56353,RMVar_hsa_circ_54952,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_13526,RMVar_hsa_circ_234834,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_359496,RMVar_hsa_circ_234835,RMVar_hsa_circ_269350,RMVar_hsa_circ_85314,RMVar_hsa_circ_272831,RMVar_hsa_circ_370666,RMVar_hsa_circ_234837,RMVar_hsa_circ_285035,RMVar_hsa_circ_127829,RMVar_hsa_circ_77999,RMVar_hsa_circ_234838,RMVar_hsa_circ_234840,RMVar_hsa_circ_234842,RMVar_hsa_circ_54836,RMVar_hsa_circ_234843,RMVar_hsa_circ_234841,RMVar_hsa_circ_234839 114668 RMVar_ID_114668 Human_SNP_ID_858954707 m1A Human chr5 + 149299563 149299563 149299563 GCTCACCGGGCTGCTCAGCCTCCTGGACCACGAGTACCTCAGCGATACCACCCTGGAAAAGAAGA GCTCACCGGGCTGCTCAGCCTCCTGGACCACGGGTACCTCAGCGATACCACCCTGGAAAAGAAGA A G AFAP1L1 Ensembl:ENSG00000157510 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:149299474..149299572 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_4816524 Human_Splice_Rec_708170,Human_Splice_Rec_708171,Human_Splice_Rec_708206,Human_Splice_Rec_708207,Human_Splice_Rec_708222,Human_Splice_Rec_708223,Human_Splice_Rec_708236,Human_Splice_Rec_708237 114669 RMVar_ID_114669 Human_SNP_ID_858976899 m1A Human chr5 + 10761070 10761070 10761070 TCTCTAGTTTCCCTTCGGGAGGCGAAGACATGACGCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG TCTCTAGTTTCCCTTCGGGAGGCGAAGACATGGCGCGGCGGGGCTTCCGCGGGGCCGAGGCGGCG A G AC012629.2 Ensembl:ENSG00000272324 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:10748226..10761275 26863196 MeRIP-seq:(Medium) rs267927 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_635459 114670 RMVar_ID_114670 Human_SNP_ID_858986921 m1A Human chr5 - 93581909 93581908 93581910 AGAGAGACCCAGAGAGAGAGAGAGAGAGAGAGACCCAGAGAGAGAGAGAGAGACCGAGAGAGAGA AGAGAGACCCAGAGAGAGAGAGAGAGAGAGA__CCCAGAGAGAGAGAGAGAGACCGAGAGAGAGA GTC G NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:93581859..93582124 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 PBCA 1 - 114671 RMVar_ID_114671 Human_SNP_ID_858988928 m1A Human chr5 - 14419950 14419950 14419950 TGGAGTGGGCGATGCACAGTGAACCACAGGGGACCAGGCCTTCTGCCGCTGGGGAGCGGTCAGTT TGGAGTGGGCGATGCACAGTGAACCACAGGGGGCCAGGCCTTCTGCCGCTGGGGAGCGGTCAGTT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:14419901..14419950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114672 RMVar_ID_114672 Human_SNP_ID_858994551 m1A Human chr5 + 14487739 14487739 14487739 AGGCAGAGGCAGACAAGATGTCAGGTACGTCCACCCCCGGGCCCTCCCTGCCTCCCCCTGGCGCG AGGCAGAGGCAGACAAGATGTCAGGTACGTCCTCCCCCGGGCCCTCCCTGCCTCCCCCTGGCGCG A T TRIO Ensembl:ENSG00000038382 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:14487692..14487875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_73425,Human_RBP_ID_249736 Human_miRNA_ID_1371442,Human_miRNA_ID_2689123,Human_miRNA_ID_2692308 RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_5235,RMVar_hsa_circ_117747,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_230387,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_7035,RMVar_hsa_circ_88005,RMVar_hsa_circ_230403,RMVar_hsa_circ_230410,RMVar_hsa_circ_85947,RMVar_hsa_circ_103203,RMVar_hsa_circ_230418,RMVar_hsa_circ_86070,RMVar_hsa_circ_6855,RMVar_hsa_circ_230423,RMVar_hsa_circ_79898,RMVar_hsa_circ_230428,RMVar_hsa_circ_113517,RMVar_hsa_circ_40021,RMVar_hsa_circ_100131,RMVar_hsa_circ_230430,RMVar_hsa_circ_230431,RMVar_hsa_circ_27394,RMVar_hsa_circ_107650,RMVar_hsa_circ_102966,RMVar_hsa_circ_123210,RMVar_hsa_circ_30472,RMVar_hsa_circ_230434,RMVar_hsa_circ_230435,RMVar_hsa_circ_84060,RMVar_hsa_circ_313382,RMVar_hsa_circ_230436,RMVar_hsa_circ_372177,RMVar_hsa_circ_230437,RMVar_hsa_circ_230438,RMVar_hsa_circ_35763,RMVar_hsa_circ_230439,RMVar_hsa_circ_347565 114673 RMVar_ID_114673 Human_SNP_ID_859002673 m1A Human chr5 - 138561658 138561658 138561658 CTAATCAGAAGGACTATCGCTCCATGCCAAAAAGCTATGCAAGATGCAGAAGTCAGCAAGAGTGA CTAATCAGAAGGACTATCGCTCCATGCCAAAAGGCTATGCAAGATGCAGAAGTCAGCAAGAGTGA T C HSPA9 Ensembl:ENSG00000113013 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1987852,Human_RBP_ID_3759005,Human_RBP_ID_7390225,Human_RBP_ID_8884928,Human_RBP_ID_9398277,Human_RBP_ID_18833505,Human_RBP_ID_22458944,Human_RBP_ID_22827264,Human_RBP_ID_24085321,Human_RBP_ID_27074617,Human_RBP_ID_27331804,Human_RBP_ID_27511836 Human_Splice_Rec_696727,Human_Splice_Rec_696757,Human_Splice_Rec_696807,Human_Splice_Rec_696815,Human_Splice_Rec_696821 Human_miRNA_ID_2092974 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833,RMVar_hsa_circ_67957,RMVar_hsa_circ_26156,RMVar_hsa_circ_272810,RMVar_hsa_circ_56353,RMVar_hsa_circ_54952,RMVar_hsa_circ_40775,RMVar_hsa_circ_127086,RMVar_hsa_circ_13526,RMVar_hsa_circ_234834,RMVar_hsa_circ_234836,RMVar_hsa_circ_110363,RMVar_hsa_circ_359496,RMVar_hsa_circ_234835,RMVar_hsa_circ_269350,RMVar_hsa_circ_85314,RMVar_hsa_circ_272831,RMVar_hsa_circ_370666,RMVar_hsa_circ_234837,RMVar_hsa_circ_285035,RMVar_hsa_circ_127829,RMVar_hsa_circ_234838,RMVar_hsa_circ_234840,RMVar_hsa_circ_234842,RMVar_hsa_circ_54836,RMVar_hsa_circ_234841,RMVar_hsa_circ_234839,RMVar_hsa_circ_234845,RMVar_hsa_circ_271745,RMVar_hsa_circ_336102,RMVar_hsa_circ_354397,RMVar_hsa_circ_375775,RMVar_hsa_circ_289097,RMVar_hsa_circ_234847,RMVar_hsa_circ_80971,RMVar_hsa_circ_234846,RMVar_hsa_circ_234844 114674 RMVar_ID_114674 Human_SNP_ID_859006680 m1A Human chr5 - 93588100 93588100 93588100 GCAGGCGCGCGGCCAGCTCGCAGATGTTCTCGATGCCCATAATGTTGTTGGGCTGCATGCACTGG GCAGGCGCGCGGCCAGCTCGCAGATGTTCTCGGTGCCCATAATGTTGTTGGGCTGCATGCACTGG T C NR2F1-AS1 RNACentral:URS00008C00C8 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:93587994..93588180 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver 114675 RMVar_ID_114675 Human_SNP_ID_859015353 m1A Human chr5 - 151800871 151800871 151800871 AAAAAAAAAAAAATCAAGACAAAAAGCTGCTTACCCTGTTGCTAAGGACTTTCTGAACAGGCTCA AAAAAAAAAAAAATCAAGACAAAAAGCTGCTTGCCCTGTTGCTAAGGACTTTCTGAACAGGCTCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151800848..151800920 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114676 RMVar_ID_114676 Human_SNP_ID_859031338 m1A Human chr5 + 170633760 170633760 170633760 GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGAGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG GGGGACGGAGGGGGGGGCGGGGGGCGGGGCGGGGGGGGGATGGGGCGGGGCGGGGTGTGGCTGTG A G KCNIP1 Ensembl:ENSG00000182132 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:170633689..170633766 26863196 MeRIP-seq:(Medium) rs1376071099 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 7 large intestine 114677 RMVar_ID_114677 Human_SNP_ID_859038051 m1A Human chr5 - 230924 230924 230924 CCTGCCCTGGTGATCATGGCCGTGCCGTCGCCAGTGCTGGTGTGGGCAGACGTGCAGCTGAAGTA CCTGCCCTGGTGATCATGGCCGTGCCGTCGCCGGTGCTGGTGTGGGCAGACGTGCAGCTGAAGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:230819..231004 26863196 MeRIP-seq:(Medium) rs1041947 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 114678 RMVar_ID_114678 Human_SNP_ID_859042854 m1A Human chr5 + 73503022 73503022 73503022 CACTTTCACCATTACAGGCCATGCTGAGACAAAGCAGCTGACAGAAATGCTACCCAGCATCTTAA CACTTTCACCATTACAGGCCATGCTGAGACAACGCAGCTGACAGAAATGCTACCCAGCATCTTAA A C BTF3 Ensembl:ENSG00000145741 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:73502973..73503046 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_646001,Human_RBP_ID_787995,Human_RBP_ID_839032,Human_RBP_ID_17302057,Human_RBP_ID_17415230,Human_RBP_ID_17532188,Human_RBP_ID_22459574,Human_RBP_ID_26826370,Human_RBP_ID_27338224 Human_Splice_Rec_661639,Human_Splice_Rec_661647,Human_Splice_Rec_661655,Human_Splice_Rec_661663,Human_Splice_Rec_661675,Human_Splice_Rec_661681,Human_Splice_Rec_661683 RMVar_hsa_circ_93375,RMVar_hsa_circ_232421,RMVar_hsa_circ_342071,RMVar_hsa_circ_371275,RMVar_hsa_circ_369464,RMVar_hsa_circ_120835,RMVar_hsa_circ_232424,RMVar_hsa_circ_232425,RMVar_hsa_circ_232426 114679 RMVar_ID_114679 Human_SNP_ID_859046251 m1A Human chr5 + 97179180 97179180 97179180 TCAAACTGCCGGGAACAATTTCATGGTTCTTCATGCCCATTTCAACCTGAAATTAAAGGAATCAT TCAAACTGCCGGGAACAATTTCATGGTTCTTCGTGCCCATTTCAACCTGAAATTAAAGGAATCAT A G LIX1-AS1 Ensembl:ENSG00000251513 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:97179131..97179249 26863196 MeRIP-seq:(Medium) rs779374505 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_312757 114680 RMVar_ID_114680 Human_SNP_ID_859053089 m1A Human chr5 - 151033658 151033658 151033658 ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCATGGCCATGGAGCACCCGCCCCCACTCCCCAAC ACTGGTCCCAGATCCGCTACCCCCCTCCCCCCCTGGCCATGGAGCACCCGCCCCCACTCCCCAAC T G TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs143590032 Functional Loss SNV ICGC,COSMIC 33..33 33 THCA,head_neck squamous_cell_carcinoma 78 head and neck Human_RBP_ID_165355 Human_Splice_Rec_711281,Human_Splice_Rec_711313,Human_Splice_Rec_711379,Human_Splice_Rec_711411,Human_Splice_Rec_711451,Human_Splice_Rec_711483,Human_Splice_Rec_711543,Human_Splice_Rec_711575 Human_miRNA_ID_2387968,Human_miRNA_ID_2392701 RMVar_hsa_circ_81305,RMVar_hsa_circ_89626,RMVar_hsa_circ_235526,RMVar_hsa_circ_78316,RMVar_hsa_circ_235527,RMVar_hsa_circ_235525 114681 RMVar_ID_114681 Human_SNP_ID_859059809 m1A Human chr5 + 134744024 134744024 134744024 ATTTGCTCCATTTCTTACTTTACAACTTGCGTACATGGGATTATACAAATATTTTCCCAAGGTAA ATTTGCTCCATTTCTTACTTTACAACTTGCGTGCATGGGATTATACAAATATTTTCCCAAGGTAA A G CAMLG Ensembl:ENSG00000164615 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:134741510..134750927 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 2 stomach Human_RBP_ID_631740,Human_RBP_ID_1038821,Human_RBP_ID_8884271,Human_RBP_ID_17302343,Human_RBP_ID_18353215,Human_RBP_ID_18832559,Human_RBP_ID_27734697 Human_Splice_Rec_693338,Human_Splice_Rec_693339,Human_Splice_Rec_693342,Human_Splice_Rec_693343 RMVar_hsa_circ_234596,RMVar_hsa_circ_270189 114682 RMVar_ID_114682 Human_SNP_ID_859079199 m1A Human chr5 - 176529092 176529092 176529092 GTGAGAGCAACGCCTGACGTGCATGTTCCCACAGGCCAACCGGACGTGTCCCATCTGCCGGGCCG GTGAGAGCAACGCCTGACGTGCATGTTCCCACCGGCCAACCGGACGTGTCCCATCTGCCGGGCCG T G RNF44 Ensembl:ENSG00000146083 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:176528880..176529129 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_943565,Human_RBP_ID_5090081,Human_RBP_ID_5396913,Human_RBP_ID_8888282,Human_RBP_ID_19124963,Human_RBP_ID_22481870,Human_RBP_ID_22553119,Human_RBP_ID_22681008,Human_RBP_ID_22745975,Human_RBP_ID_26791811 RMVar_hsa_circ_75927,RMVar_hsa_circ_236381 114683 RMVar_ID_114683 Human_SNP_ID_859091980 m1A Human chr5 + 34826427 34826427 34826427 CTACTCAACAAGCTCATCCAAAAGGCAGAGTCAGCAGCTGGAGGCGCTGCAGCAGCAAGTCAAAC CTACTCAACAAGCTCATCCAAAAGGCAGAGTCGGCAGCTGGAGGCGCTGCAGCAGCAAGTCAAAC A G RAI14 Ensembl:ENSG00000039560 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:34826376..34829784 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_641674,Human_Splice_Rec_641675,Human_Splice_Rec_641748,Human_Splice_Rec_641749,Human_Splice_Rec_641782,Human_Splice_Rec_641783,Human_Splice_Rec_641856,Human_Splice_Rec_641857,Human_Splice_Rec_641926,Human_Splice_Rec_641927,Human_Splice_Rec_642008,Human_Splice_Rec_642009,Human_Splice_Rec_642051,Human_Splice_Rec_642055 Human_miRNA_ID_1007521 RMVar_hsa_circ_32419,RMVar_hsa_circ_368664,RMVar_hsa_circ_230774,RMVar_hsa_circ_336330,RMVar_hsa_circ_306930,RMVar_hsa_circ_230778,RMVar_hsa_circ_2916,RMVar_hsa_circ_25780,RMVar_hsa_circ_356022,RMVar_hsa_circ_367804,RMVar_hsa_circ_16671,RMVar_hsa_circ_230781 114684 RMVar_ID_114684 Human_SNP_ID_859096884 m1A Human chr5 + 16673733 16673716 16673733 GAGTTGATGGTGATCTTGCAGGAGCCGCCGCCATGGCAATAGACCGTGGATGTCATTTCCTGCCT GAGTTGATGGTGATCT_________________TGGCAATAGACCGTGGATGTCATTTCCTGCCT TTGCAGGAGCCGCCGCCA T AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16673701..16673775 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 17..33 33 BRCA 1 - 114685 RMVar_ID_114685 Human_SNP_ID_859098706 m1A Human chr5 + 16616954 16616954 16616954 GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGAGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC GGAGCCGGGCATCCCTCCTCGGCGTGCTCCGGGGGCGCCGGGCTCGCCATCTTCAGCTGTGCTTC A G AC024588.1 Ensembl:ENSG00000246214 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:16616698..16617104;chr5:16616660..16617058 26863196 MeRIP-seq:(Medium) rs773314283 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 114686 RMVar_ID_114686 Human_SNP_ID_859100600 m1A Human chr5 + 10358061 10358061 10358061 GCGATCTTGGCTCACTAGGGGTCGCAGTTTTAAATATAGCAGTAAAGGAAGGCCTCACTGAGAAG GCGATCTTGGCTCACTAGGGGTCGCAGTTTTACATATAGCAGTAAAGGAAGGCCTCACTGAGAAG A C MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:10358054..10358350 26863196 MeRIP-seq:(Medium) rs1290604996 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_15252327 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215 114687 RMVar_ID_114687 Human_SNP_ID_859134957 m1A Human chr5 - 134758901 134758901 134758901 CGACCGCGGGAATACTGGTGCCCTTGAGTACCACGCACAGGCGAACCGGACAAACAAGGAGGCTG CGACCGCGGGAATACTGGTGCCCTTGAGTACCGCGCACAGGCGAACCGGACAAACAAGGAGGCTG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:134758801..134759009 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PEME 1 - 114688 RMVar_ID_114688 Human_SNP_ID_859141803 m1A Human chr5 + 141636815 141636798 141636816 TTGGCCATGGTGCCGGCGGGAGCAGGCCCCGCACCTCCGCCGCCCGCCGCCCGCGGCCGCCGCCA TTGGCCATGGTGCCGG__________________CTCCGCCGCCCGCCGCCCGCGGCCGCCGCCA GCGGGAGCAGGCCCCGCAC G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141636742..141636850 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 17..34 33 READ 1 - 114689 RMVar_ID_114689 Human_SNP_ID_859183707 m1A Human chr5 - 177496477 177496477 177496477 GATTCCTTCAAAGTAGTGCTGGAGGGGCCAGCACCTTGGGGCTTCCGGCTGCAAGGGGGCAAGGA GATTCCTTCAAAGTAGTGCTGGAGGGGCCAGCGCCTTGGGGCTTCCGGCTGCAAGGGGGCAAGGA T C PDLIM7 Ensembl:ENSG00000196923 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177492964..177496539 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_639031,Human_RBP_ID_789001,Human_RBP_ID_5397763,Human_RBP_ID_9398722,Human_RBP_ID_23050458,Human_RBP_ID_26351830,Human_RBP_ID_27079178 Human_Splice_Rec_725446,Human_Splice_Rec_725447,Human_Splice_Rec_725472,Human_Splice_Rec_725473,Human_Splice_Rec_725496,Human_Splice_Rec_725497,Human_Splice_Rec_725520,Human_Splice_Rec_725521,Human_Splice_Rec_725552,Human_Splice_Rec_725553,Human_Splice_Rec_725568,Human_Splice_Rec_725569,Human_Splice_Rec_725582,Human_Splice_Rec_725583,Human_Splice_Rec_725596,Human_Splice_Rec_725597,Human_Splice_Rec_725605,Human_Splice_Rec_725625,Human_Splice_Rec_725636,Human_Splice_Rec_725637,Human_Splice_Rec_725641 RMVar_hsa_circ_50409,RMVar_hsa_circ_348647 114690 RMVar_ID_114690 Human_SNP_ID_859186426 m1A Human chr5 - 178205872 178205872 178205872 GTAAAATAGTCTTTTAAATCTTTTTTGCTAGTATCCCAGCTCAGGCCACCAACGAACATTTTTCT GTAAAATAGTCTTTTAAATCTTTTTTGCTAGTGTCCCAGCTCAGGCCACCAACGAACATTTTTCT T C RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:178205800..178205950 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 9 caecum,large intestine Human_RBP_ID_2920192 114691 RMVar_ID_114691 Human_SNP_ID_859191831 m1A Human chr5 + 181237676 181237676 181237676 GGGGTGGTTCTGCCTTGCTGCTGGTACTGATAACTTCTTGCTTCAGTTCATCTACAATGATCTTT GGGGTGGTTCTGCCTTGCTGCTGGTACTGATACCTTCTTGCTTCAGTTCATCTACAATGATCTTT A C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181237601..181237675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_3767500 114692 RMVar_ID_114692 Human_SNP_ID_859196614 m1A Human chr5 - 93584918 93584918 93584918 GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGAGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT GAGGGGAAGGGGAAGGGGAAGGGGGGAGGGGGGGGGGGCGGGGGGCCCGCCGGGCGCCCCGGGGT T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr5:93584818..93584935;chr5:93584818..93584918 26863410 MeRIP-seq:(Medium) rs898353185 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8213172,Human_RBP_ID_8268030,Human_RBP_ID_26792092 114693 RMVar_ID_114693 Human_SNP_ID_859209426 m1A Human chr5 - 141573741 141573741 141573741 CCTTTGCCTGGGAGTGCTGGAATTCCCCCCCCACCTCCTCCCTTGCCTGGAGAAGCAGGAATGCC CCTTTGCCTGGGAGTGCTGGAATTCCCCCCCCCCCTCCTCCCTTGCCTGGAGAAGCAGGAATGCC T G DIAPH1 Ensembl:ENSG00000131504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141573698..141573878 26863196 MeRIP-seq:(Medium) rs1242514245 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_633742,Human_RBP_ID_4814110,Human_RBP_ID_5133877,Human_RBP_ID_9306715,Human_RBP_ID_17090116,Human_RBP_ID_21129299,Human_RBP_ID_26522561 Human_miRNA_ID_2028645,Human_miRNA_ID_2689182,Human_miRNA_ID_2692369 RMVar_hsa_circ_97418,RMVar_hsa_circ_119624,RMVar_hsa_circ_5992,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_76374,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_91511,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091,RMVar_hsa_circ_110882,RMVar_hsa_circ_127283,RMVar_hsa_circ_348962,RMVar_hsa_circ_119447,RMVar_hsa_circ_235092,RMVar_hsa_circ_235093,RMVar_hsa_circ_235094,RMVar_hsa_circ_95234,RMVar_hsa_circ_356274,RMVar_hsa_circ_235095,RMVar_hsa_circ_235096 114694 RMVar_ID_114694 Human_SNP_ID_859224709 m1A Human chr5 - 309988 309961 309989 GGGGACGGCGGCCATCACTGGGGTGCACGGGCACGGCGGCCATCACTGGTGTGCACGGGGACGGC GGGGACGGCGGCCATCACTGGGGTGCACGGG____________________________GACGGC CCCCGTGCACACCAGTGATGGCCGCCGTG C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:309907..310075 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..59 33 CHOL 1 - 114695 RMVar_ID_114695 Human_SNP_ID_859227292 m1A Human chr5 - 40746967 40746967 40746967 AGAGGAAAATTGGTGAGAAGGTCTCAAAGGTCACTTCCCAGCAGTTTGAAGCTGAAGCTGCTGAT AGAGGAAAATTGGTGAGAAGGTCTCAAAGGTCTCTTCCCAGCAGTTTGAAGCTGAAGCTGCTGAT T A TTC33 Ensembl:ENSG00000113638 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:40746916..40747058 26863196 MeRIP-seq:(Medium) rs1406015187 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma,lung large_cell_carcinoma 8 lung Human_RBP_ID_4855188 Human_Splice_Rec_646546,Human_Splice_Rec_646552,Human_Splice_Rec_646556,Human_Splice_Rec_646560,Human_Splice_Rec_646568,Human_Splice_Rec_646572,Human_Splice_Rec_646578 RMVar_hsa_circ_305529,RMVar_hsa_circ_231177,RMVar_hsa_circ_378010,RMVar_hsa_circ_48627,RMVar_hsa_circ_231181 114696 RMVar_ID_114696 Human_SNP_ID_859252744 m1A Human chr5 - 180494649 180494649 180494649 ATACCAGTCCCGCCCGCTGCTGCAGCGCCGCCACCGCCGCCGCTCCTCTGCCGCCTTAGTCGCTG ATACCAGTCCCGCCCGCTGCTGCAGCGCCGCCGCCGCCGCCGCTCCTCTGCCGCCTTAGTCGCTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:180494626..180494650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114697 RMVar_ID_114697 Human_SNP_ID_859258344 m1A Human chr5 + 31532367 31532367 31532367 TTTCCCGGGTCTTCTCCAGCTGCCACCGCTTTACTGCAAAACTGACGGGCGCAAAAACATGAGTG TTTCCCGGGTCTTCTCCAGCTGCCACCGCTTTGCTGCAAAACTGACGGGCGCAAAAACATGAGTG A G C5orf22 Ensembl:ENSG00000082213 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:31532319..31532475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4845641,Human_RBP_ID_5509548,Human_RBP_ID_18841144 114698 RMVar_ID_114698 Human_SNP_ID_859304823 m1A Human chr5 - 73447055 73447055 73447055 CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCAGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA CTCGTGGCCGCCGCGGCCGCCGCCGCCTCCTCGGTCTCCTCGTCCGCCGCCTTGGGGACTCTGCA T C FOXD1 Ensembl:ENSG00000251493 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2972191 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_250552,Human_RBP_ID_1141481,Human_RBP_ID_5103333,Human_RBP_ID_8267815,Human_RBP_ID_17303586,Human_RBP_ID_17416990,Human_RBP_ID_17532539 Human_miRNA_ID_1829937,Human_miRNA_ID_1829972,Human_miRNA_ID_1853777,Human_miRNA_ID_1880419,Human_miRNA_ID_1909613 GWAS_ID_9250 114699 RMVar_ID_114699 Human_SNP_ID_859320309 m1A Human chr5 + 154941131 154941131 154941131 GGAGGGCGAAAGATGGCGGCGGCAGTACTGGGACAGTTGGGTAAGGATTTCTTAGTGGTTAAGCG GGAGGGCGAAAGATGGCGGCGGCAGTACTGGGGCAGTTGGGTAAGGATTTCTTAGTGGTTAAGCG A G MRPL22 Ensembl:ENSG00000082515 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:154941076..154941301;chr5:154941076..154941332 26863196 MeRIP-seq:(Medium) rs1293892096 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_789157,Human_RBP_ID_5509143 Human_Splice_Rec_714031,Human_Splice_Rec_714043,Human_Splice_Rec_714063 114700 RMVar_ID_114700 Human_SNP_ID_859338565 m1A Human chr5 - 151045892 151045883 151045892 AGAGGTGGTGGCCTTGGGCGCAGCCGAGAAGAAGGTGAAGATGCTGGAGCAGCAGCGCAGTGAGG AGAGGTGGTGGCCTTGGGCGCAGCCGAGAAGA_________TGCTGGAGCAGCAGCGCAGTGAGG ATCTTCACCT A TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151037426..151045975 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..41 33 PAAD 1 - Human_RBP_ID_250183,Human_RBP_ID_839122,Human_RBP_ID_944719,Human_RBP_ID_19016080,Human_RBP_ID_27827023 Human_Splice_Rec_711268,Human_Splice_Rec_711269,Human_Splice_Rec_711300,Human_Splice_Rec_711301,Human_Splice_Rec_711332,Human_Splice_Rec_711333,Human_Splice_Rec_711366,Human_Splice_Rec_711367,Human_Splice_Rec_711398,Human_Splice_Rec_711399,Human_Splice_Rec_711430,Human_Splice_Rec_711431,Human_Splice_Rec_711470,Human_Splice_Rec_711471,Human_Splice_Rec_711498,Human_Splice_Rec_711499,Human_Splice_Rec_711530,Human_Splice_Rec_711531,Human_Splice_Rec_711562,Human_Splice_Rec_711563,Human_Splice_Rec_711592,Human_Splice_Rec_711593,Human_Splice_Rec_711618,Human_Splice_Rec_711619,Human_Splice_Rec_711634,Human_Splice_Rec_711639,Human_Splice_Rec_711654 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_235530,RMVar_hsa_circ_361863,RMVar_hsa_circ_349118 114701 RMVar_ID_114701 Human_SNP_ID_859377501 m1A Human chr5 - 190384 190383 190385 GGAGAGACAGAGACTAAGAGAGAGAGAGAGAGACTGGTAGGCAGAGACAGAGACTGAGAAAGACA GGAGAGACAGAGACTAAGAGAGAGAGAGAGA__CTGGTAGGCAGAGACAGAGACTGAGAAAGACA GTC G lnc-CCDC127-3,lnc-CCDC127-3:2,lnc-CCDC127-3:3 RNACentral:URS00008BCB82,RNACentral:URS00009B2EFE,RNACentral:URS00008C1537 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:190374..190519 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 ESCA 1 - 114702 RMVar_ID_114702 Human_SNP_ID_859413249 m1A Human chr5 + 134773850 134773850 134773850 AGAGATGAAACAAGGGAAAAAGTGGAGTTTAGAGGACGATGATGGTATATTTTTTAGCCTAATAG AGAGATGAAACAAGGGAAAAAGTGGAGTTTAGGGGACGATGATGGTATATTTTTTAGCCTAATAG A G DDX46 Ensembl:ENSG00000145833 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:134758776..134777790 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_12452,Human_RBP_ID_942965,Human_RBP_ID_8884279,Human_RBP_ID_15303162,Human_RBP_ID_19015836,Human_RBP_ID_23038698,Human_RBP_ID_23116253,Human_RBP_ID_24548203,Human_RBP_ID_24554379,Human_RBP_ID_25856011,Human_RBP_ID_26351279,Human_RBP_ID_27826741 Human_Splice_Rec_693351,Human_Splice_Rec_693373,Human_Splice_Rec_693415,Human_Splice_Rec_693455,Human_Splice_Rec_693489 RMVar_hsa_circ_55145,RMVar_hsa_circ_70760,RMVar_hsa_circ_367645,RMVar_hsa_circ_342231,RMVar_hsa_circ_355586,RMVar_hsa_circ_356628,RMVar_hsa_circ_71771,RMVar_hsa_circ_63579,RMVar_hsa_circ_67145,RMVar_hsa_circ_60426,RMVar_hsa_circ_234598 114703 RMVar_ID_114703 Human_SNP_ID_859468295 m1A Human chr5 - 140676757 140676757 140676757 TGTGGGCAGTGTGGCTGCTGGAGGACGCTATGATGGGCTAGTGGGCATGTTCGACCCCAAAGGGC TGTGGGCAGTGTGGCTGCTGGAGGACGCTATGTTGGGCTAGTGGGCATGTTCGACCCCAAAGGGC T A HARS1 Ensembl:ENSG00000170445 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:140676619..140676850;chr5:140676621..140677100;chr5:140676615..140676916;chr5:140676626..140676900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 brain astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III,lung non_small_cell_carcinoma 16 lung,brain Human_RBP_ID_4813583,Human_RBP_ID_15328091,Human_RBP_ID_17157816,Human_RBP_ID_27075330 RMVar_hsa_circ_107708,RMVar_hsa_circ_118846,RMVar_hsa_circ_90848,RMVar_hsa_circ_235048,RMVar_hsa_circ_235049,RMVar_hsa_circ_235047,RMVar_hsa_circ_54543,RMVar_hsa_circ_305418,RMVar_hsa_circ_364806 114704 RMVar_ID_114704 Human_SNP_ID_859482001 m1A Human chr5 - 132937176 132937176 132937176 TGTTTCTTTTCATAGCAACATGAACCGTGAAGACCGGAATGTGCTGCGTATGAAAGAACGGGAAA TGTTTCTTTTCATAGCAACATGAACCGTGAAGGCCGGAATGTGCTGCGTATGAAAGAACGGGAAA T C AFF4 Ensembl:ENSG00000072364 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:132934685..132963534 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_RBP_ID_838639,Human_RBP_ID_944506,Human_RBP_ID_9399349,Human_RBP_ID_15295828,Human_RBP_ID_22680680,Human_RBP_ID_24547989,Human_RBP_ID_24561983,Human_RBP_ID_25933320 Human_Splice_Rec_691878,Human_Splice_Rec_691918,Human_Splice_Rec_691988,Human_Splice_Rec_692000,Human_Splice_Rec_692008 RMVar_hsa_circ_79415,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_70765,RMVar_hsa_circ_274107,RMVar_hsa_circ_234407,RMVar_hsa_circ_234408,RMVar_hsa_circ_365681,RMVar_hsa_circ_234411 114705 RMVar_ID_114705 Human_SNP_ID_859482267 m1A Human chr5 + 65563350 65563350 65563350 CGGAAAGTGGTAGCGATTTTCAGCAGAGACGTAGAAGGCGCCGGGACCCGGAGGAACCGGAAAAA CGGAAAGTGGTAGCGATTTTCAGCAGAGACGTGGAAGGCGCCGGGACCCGGAGGAACCGGAAAAA A G PPWD1 Ensembl:ENSG00000113593 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:65563301..65563528 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_249960,Human_RBP_ID_839107,Human_RBP_ID_4835637,Human_RBP_ID_9399115,Human_RBP_ID_15488612,Human_RBP_ID_22301996,Human_RBP_ID_24547928,Human_RBP_ID_27825416 RMVar_hsa_circ_101184,RMVar_hsa_circ_231843,RMVar_hsa_circ_95606,RMVar_hsa_circ_231844 114706 RMVar_ID_114706 Human_SNP_ID_859483791 m1A Human chr5 - 16701411 16701411 16701411 CAGCCAGCCCTACCCAGAGGAGGAGGTCGATGAGGGCTTCGAAGCCGACGACGACGCCTTCAAGG CAGCCAGCCCTACCCAGAGGAGGAGGTCGATGCGGGCTTCGAAGCCGACGACGACGCCTTCAAGG T G MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:16701251..16701600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_75551,Human_RBP_ID_8887679 RMVar_hsa_circ_42338,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230498,RMVar_hsa_circ_264947,RMVar_hsa_circ_230499,RMVar_hsa_circ_126247,RMVar_hsa_circ_97329,RMVar_hsa_circ_107631,RMVar_hsa_circ_230501,RMVar_hsa_circ_110190,RMVar_hsa_circ_289935,RMVar_hsa_circ_230502,RMVar_hsa_circ_117125,RMVar_hsa_circ_95398,RMVar_hsa_circ_3584,RMVar_hsa_circ_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_74659,RMVar_hsa_circ_44006,RMVar_hsa_circ_120862,RMVar_hsa_circ_330089,RMVar_hsa_circ_230510 114707 RMVar_ID_114707 Human_SNP_ID_859486082 m1A Human chr5 - 311363 311363 311363 ACGATGCAGCCCTGGATGAAGTCGTCGAAGGCAATCTGCCCCCGTCCCTGCCTGTCAAACTTTCG ACGATGCAGCCCTGGATGAAGTCGTCGAAGGCGATCTGCCCCCGTCCCTGCCTGTCAAACTTTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:311315..311437 26863196 MeRIP-seq:(Medium) rs2244029 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 21 head and neck,large intestine GWAS_ID_6659 114708 RMVar_ID_114708 Human_SNP_ID_859507014 m1A Human chr5 - 38832114 38832114 38832114 AGAGAGACAGAGAGACAGAGAGAGAGACAGAGAGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAA AGAGAGACAGAGAGACAGAGAGAGAGACAGAGGGGAGAGAGAGGAGAGAGAGAGGAGAGAGAGAA T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr5:38831988..38832261;chr5:38832070..38832199 26863196 MeRIP-seq:(Medium) rs1223255978 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_25895761 114709 RMVar_ID_114709 Human_SNP_ID_859565709 m1A Human chr5 - 140671310 140671310 140671310 ACCTCCTGTGGTCTGCTGGGGCTGAGGCAGGTACCATGGTTAAACAGTGACTCCATTCTTTCTCC ACCTCCTGTGGTCTGCTGGGGCTGAGGCAGGTGCCATGGTTAAACAGTGACTCCATTCTTTCTCC T C DND1 Ensembl:ENSG00000256453 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:140671222..140671322 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 2 pancreas 114710 RMVar_ID_114710 Human_SNP_ID_859585980 m1A Human chr5 - 74767339 74767339 74767339 CTCCTTACCATGGTGACGGCCGCAGAGCCGCCAGGAGCAGCCGCTGGAGTGCGAAAACGCTCTCA CTCCTTACCATGGTGACGGCCGCAGAGCCGCCTGGAGCAGCCGCTGGAGTGCGAAAACGCTCTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:74767288..74767401 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney 114711 RMVar_ID_114711 Human_SNP_ID_859713751 m1A Human chr5 + 72908948 72908946 72908948 AGTTACAACTCCGCAGTGGATGTGAAGAAGCAAAAAAAAAAAAATCTATTCAGTCTACTCACAAA AGTTACAACTCCGCAGTGGATGTGAAGAAGC__AAAAAAAAAAATCTATTCAGTCTACTCACAAA CAA C TNPO1 Ensembl:ENSG00000083312 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:72908901..72909025 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - Human_RBP_ID_645779,Human_RBP_ID_8621512,Human_RBP_ID_17301170,Human_RBP_ID_17531214 Human_miRNA_ID_186011,Human_miRNA_ID_2004575 RMVar_hsa_circ_123423,RMVar_hsa_circ_232367 114712 RMVar_ID_114712 Human_SNP_ID_859737835 m1A Human chr5 + 141319305 141319305 141319305 GTAGCTGTCTCTCCAGATCTTCCTCCGTGTCAATGATGTTTATATCTTCTTCATCTTGATGCTGG GTAGCTGTCTCTCCAGATCTTCCTCCGTGTCACTGATGTTTATATCTTCTTCATCTTGATGCTGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:141319254..141319329 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114713 RMVar_ID_114713 Human_SNP_ID_859746738 m1A Human chr5 - 138766593 138766593 138766593 TTCTCCTCCGTACCTCAGTAAACACCTCACTCACCCTACTAACCCCCTTCCTGCTCTCAGGGCTC TTCTCCTCCGTACCTCAGTAAACACCTCACTCGCCCTACTAACCCCCTTCCTGCTCTCAGGGCTC T C RF00017-4932 RNACentral:URS000096C9DE SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:138766589..138766710 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114714 RMVar_ID_114714 Human_SNP_ID_859756222 m1A Human chr5 + 135029129 135029129 135029129 CGACAGCGGGCTCATGGAGTTGAAGAAGGTGAAGCTCTTGGTGGAGAGCGGCGCTGGCGCCAGGC CGACAGCGGGCTCATGGAGTTGAAGAAGGTGAGGCTCTTGGTGGAGAGCGGCGCTGGCGCCAGGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:135028916..135029259 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 114715 RMVar_ID_114715 Human_SNP_ID_859781535 m1A Human chr5 - 160415300 160415300 160415300 TAAGTTTCACTTCTTTTCCTAGAGGAGGCCAGATAACCATGTCAGCCACAGTTGTAGATGCAGTT TAAGTTTCACTTCTTTTCCTAGAGGAGGCCAGTTAACCATGTCAGCCACAGTTGTAGATGCAGTT T A SLU7 Ensembl:ENSG00000164609 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA heat shock 4h chr5:160415126..160415325 31548705,26863196 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_5151359,Human_RBP_ID_26351706,Human_RBP_ID_27826084 Human_Splice_Rec_716186,Human_Splice_Rec_716228,Human_Splice_Rec_716236,Human_Splice_Rec_716244,Human_Splice_Rec_716252,Human_Splice_Rec_716256 114716 RMVar_ID_114716 Human_SNP_ID_859782152 m1A Human chr5 - 66175031 66175031 66175031 TTAGCACAAGCTCCCAACCTACCTCCTGGGGGACGGAGATCTAGAAGATTTCCTTTTTATGGTTT TTAGCACAAGCTCCCAACCTACCTCCTGGGGGGCGGAGATCTAGAAGATTTCCTTTTTATGGTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:66174885..66175077 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114717 RMVar_ID_114717 Human_SNP_ID_859782394 m1A Human chr5 + 172641321 172641321 172641321 CGCCCGTGCAGCTGCGATGCCCCGGAGCGTCGACCCCGGTCCTGGTCCCTGGCCCGCCGCGTAAT CGCCCGTGCAGCTGCGATGCCCCGGAGCGTCGCCCCCGGTCCTGGTCCCTGGCCCGCCGCGTAAT A C NEURL1B Ensembl:ENSG00000214357 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr5:172641274..172641402;chr5:172641276..172641435;chr5:172641280..172641380 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114718 RMVar_ID_114718 Human_SNP_ID_859799839 m1A Human chr5 - 81301466 81301466 81301466 AGTGATGGGATGGCCCTGTGCAGGACGCCGACACGAAAAGATGAAGAGTTCAATCCGTGCTGTCT AGTGATGGGATGGCCCTGTGCAGGACGCCGACGCGAAAAGATGAAGAGTTCAATCCGTGCTGTCT T C CKMT2-AS1 Ensembl:ENSG00000247572 lincRNA exon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr5:81301273..81301481;chr5:81301286..81301504;chr5:81301293..81301507 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_5104082 114719 RMVar_ID_114719 Human_SNP_ID_859810075 m1A Human chr5 - 134411752 134411750 134411752 CGGAGCAGTTCCGCTCCTACTCAGAGAGCGAGAAGCAATGGAAGGCCCGCATGGAATTCATCCTG CGGAGCAGTTCCGCTCCTACTCAGAGAGCGAG__GCAATGGAAGGCCCGCATGGAATTCATCCTG CTT C CDKN2AIPNL Ensembl:ENSG00000237190 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:134411702..134411849 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 OV 1 - Human_RBP_ID_4847171 114720 RMVar_ID_114720 Human_SNP_ID_859812587 m1A Human chr5 + 179893433 179893433 179893433 TCGGGGAAGAGCAGGGTGGCGTTCTTCTCCAGACGCGTTATGTCCACCCACTGCACCACGAGGCT TCGGGGAAGAGCAGGGTGGCGTTCTTCTCCAGGCGCGTTATGTCCACCCACTGCACCACGAGGCT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179893383..179894525 32194978 MeRIP-seq:(Medium) rs759139394 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 2 head and neck 114721 RMVar_ID_114721 Human_SNP_ID_859855483 m1A Human chr5 - 44809477 44809477 44809477 TTGACACCAGCTGATCCAGGAAGGGCAAAGATATGACCTCGCTCTCCTCGTAACGGTGCACGCGC TTGACACCAGCTGATCCAGGAAGGGCAAAGATGTGACCTCGCTCTCCTCGTAACGGTGCACGCGC T C MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10,MRPS30-DT:11 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5D30C,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:44809426..44809569 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 114722 RMVar_ID_114722 Human_SNP_ID_859865092 m1A Human chr5 + 172834432 172834432 172834432 CCGGCGGCGGCACGATGCCCTTTGACTTCAGGAGGTGAGTGTGGCGACCCCGGCCAGTCGGGAGT CCGGCGGCGGCACGATGCCCTTTGACTTCAGGGGGTGAGTGTGGCGACCCCGGCCAGTCGGGAGT A G ERGIC1 Ensembl:ENSG00000113719 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:172834351..172834607 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_945452,Human_RBP_ID_4846153,Human_RBP_ID_24096921 Human_Splice_Rec_721179,Human_Splice_Rec_721197,Human_Splice_Rec_721203,Human_Splice_Rec_721215,Human_Splice_Rec_721225 RMVar_hsa_circ_236263,RMVar_hsa_circ_122533 114723 RMVar_ID_114723 Human_SNP_ID_859867634 m1A Human chr5 + 648483 648457 648483 TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTATGACTGTGAGGTGTGACTGTGAGGTGTGGACT TGAGGTG__________________________TGACTGTGAGGTGTGACTGTGAGGTGTGGACT GTGACTGTGAGGTGTGACTGTGAGGTA G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:648441..648545;chr5:648426..648558 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 8..33 33 PRAD 2 - Human_RBP_ID_5655494,Human_RBP_ID_24124148 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 114724 RMVar_ID_114724 Human_SNP_ID_859867712 m1A Human chr5 + 181234938 181234938 181234938 CCCCAGGCCCCTGCTTCTCCCTCTAGGAGCCTAAAGAACCCTCCTGGCCTCCAGCTCAGCCTTCT CCCCAGGCCCCTGCTTCTCCCTCTAGGAGCCTGAAGAACCCTCCTGGCCTCCAGCTCAGCCTTCT A G TRIM41 Ensembl:ENSG00000146063 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181234888..181235010 26863196 MeRIP-seq:(Medium) rs1199037620 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_17529585,Human_RBP_ID_25887265,Human_RBP_ID_26791981 Human_Splice_Rec_732158,Human_Splice_Rec_732159,Human_Splice_Rec_732170,Human_Splice_Rec_732171 Human_miRNA_ID_2992579 RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 114725 RMVar_ID_114725 Human_SNP_ID_859874401 m1A Human chr5 + 53603513 53603513 53603513 CACAGGACCAGACTCAAGACACACAACTCATAACAGTTGATGAAAAATTGGTAAGGATTTTCTAC CACAGGACCAGACTCAAGACACACAACTCATAGCAGTTGATGAAAAATTGGTAAGGATTTTCTAC A G NDUFS4 Ensembl:ENSG00000164258 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:53573724..53604736 32194978 MeRIP-seq:(Medium) rs756821245 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 1 lung Human_RBP_ID_1041758,Human_RBP_ID_1655205,Human_RBP_ID_8617074,Human_RBP_ID_9399095,Human_RBP_ID_15457376,Human_RBP_ID_17301969,Human_RBP_ID_18049299 Human_Splice_Rec_650505,Human_Splice_Rec_650512,Human_Splice_Rec_650513,Human_Splice_Rec_650522,Human_Splice_Rec_650523,Human_Splice_Rec_650530,Human_Splice_Rec_650531,Human_Splice_Rec_650540,Human_Splice_Rec_650541 RMVar_hsa_circ_110132,RMVar_hsa_circ_231352,RMVar_hsa_circ_80678,RMVar_hsa_circ_90741,RMVar_hsa_circ_231353,RMVar_hsa_circ_334693,RMVar_hsa_circ_358771,RMVar_hsa_circ_370273,RMVar_hsa_circ_270015,RMVar_hsa_circ_231354,RMVar_hsa_circ_231356,RMVar_hsa_circ_231357,RMVar_hsa_circ_231358,RMVar_hsa_circ_231355 114726 RMVar_ID_114726 Human_SNP_ID_859879247 m1A Human chr5 + 151259878 151259878 151259878 TCATCGTTCCTGGAAATGTGACCCTCAGTGTCATGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT TCATCGTTCCTGGAAATGTGACCCTCAGTGTCGTGGGCAGCACCAGTGTCCCCCTGAGTTCTCCT A G GM2A Ensembl:ENSG00000196743 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs153478 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,COCA,central_nervous_system oligodendroglioma_Grade_II 6 brain Human_RBP_ID_22459005,Human_RBP_ID_22771489 Human_Splice_Rec_712015,Human_Splice_Rec_712019,Human_Splice_Rec_712023 Clinvar_Rec_430 GWAS_ID_10038,GWAS_ID_10039,GWAS_ID_10040,GWAS_ID_10041,GWAS_ID_10042,GWAS_ID_10043 114727 RMVar_ID_114727 Human_SNP_ID_859884555 m1A Human chr5 + 139680575 139680575 139680575 GCTCCCAGGATGCCGGCGGCAGTAGCAGCAGCAGCACCAATGGCAGCGGTGGCAGTGGCAGCAGT GCTCCCAGGATGCCGGCGGCAGTAGCAGCAGCCGCACCAATGGCAGCGGTGGCAGTGGCAGCAGT A C CXXC5 Ensembl:ENSG00000171604 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:139680525..139680698 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_4812619,Human_RBP_ID_9306664,Human_RBP_ID_22100514 RMVar_hsa_circ_35380 114728 RMVar_ID_114728 Human_SNP_ID_859913474 m1A Human chr5 + 80654693 80654693 80654693 GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCAGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG GGAACTGCGGCCGCGGGCTCGCGCTCCTCGCCGGGCCCTGCCGCCGGGCTGCCATCCTTGCCCTG A G MSH3 Ensembl:ENSG00000113318 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1105524 Functional Loss SNV ICGC,COSMIC 33..33 33 large_intestine adenocarcinoma,CHOL 39 large intestine Human_RBP_ID_4845808 114729 RMVar_ID_114729 Human_SNP_ID_859914545 m1A Human chr5 - 179610493 179610493 179610493 GAAGCCCGTGGGAAGGGAGGGTAGGGTCGCGGACAAGGTATGTGTATAGAAGGTGGAGAAGGATG GAAGCCCGTGGGAAGGGAGGGTAGGGTCGCGGGCAAGGTATGTGTATAGAAGGTGGAGAAGGATG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:179610389..179610567 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114730 RMVar_ID_114730 Human_SNP_ID_859928972 m1A Human chr5 + 73498512 73498512 73498512 CTAATCTCAGGTGGTCCACCCGAGACCCCTTGAGCACCAACCCTAGTCCCCCGCGCGGCCCCTTA CTAATCTCAGGTGGTCCACCCGAGACCCCTTGCGCACCAACCCTAGTCCCCCGCGCGGCCCCTTA A C BTF3 Ensembl:ENSG00000145741 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:73498450..73498532 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_75695,Human_RBP_ID_645988,Human_RBP_ID_839249,Human_RBP_ID_945490,Human_RBP_ID_1213604,Human_RBP_ID_1657849,Human_RBP_ID_1999327,Human_RBP_ID_3777022,Human_RBP_ID_4838900,Human_RBP_ID_5450055,Human_RBP_ID_5476898,Human_RBP_ID_5509883,Human_RBP_ID_8621626,Human_RBP_ID_15511168,Human_RBP_ID_17301190,Human_RBP_ID_17662666,Human_RBP_ID_18052445,Human_RBP_ID_18846802,Human_RBP_ID_22100454,Human_RBP_ID_22460082,Human_RBP_ID_24115436,Human_RBP_ID_26705274,Human_RBP_ID_26826363,Human_RBP_ID_27084154,Human_RBP_ID_27338220 Human_Splice_Rec_661635,Human_Splice_Rec_661645,Human_Splice_Rec_661651,Human_Splice_Rec_661671,Human_Splice_Rec_661677 Human_miRNA_ID_727894,Human_miRNA_ID_2249955,Human_miRNA_ID_2293679 RMVar_hsa_circ_93375,RMVar_hsa_circ_232421 114731 RMVar_ID_114731 Human_SNP_ID_860034266 m1A Human chr5 + 157731528 157731528 157731528 CTCTGAGACGGTACCTGAGATTGGGGGCGACCATGGCAAAAAGCAAGTTCGAGTACGTGAGGGAC CTCTGAGACGGTACCTGAGATTGGGGGCGACCTTGGCAAAAAGCAAGTTCGAGTACGTGAGGGAC A T THG1L Ensembl:ENSG00000113272 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:157731477..157731561 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_18837188,Human_RBP_ID_26826788 Human_miRNA_ID_2004646 RMVar_hsa_circ_76787,RMVar_hsa_circ_105432,RMVar_hsa_circ_235847,RMVar_hsa_circ_235848 114732 RMVar_ID_114732 Human_SNP_ID_860044591 m1A Human chr5 + 55307860 55307858 55307860 TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCG TAGGTCGGAAAGGAAAGGAAAGAAAAGCAGG__AAAAAAAAAAAGTCAGGGGAACATTTTTGTCG GAA G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:55307809..55307959 26863196 MeRIP-seq:(Medium) rs879182172 Functional Loss DEL TCGA 32..33 33 STAD,UCEC 2 - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 114733 RMVar_ID_114733 Human_SNP_ID_860098969 m1A Human chr5 - 151036903 151036903 151036903 TTTCCTGATTCCAGGCCCTGGAGGAAGCACTGAGCATCCAAACCCCGCCATCATCTCCACCAACA TTTCCTGATTCCAGGCCCTGGAGGAAGCACTGTGCATCCAAACCCCGCCATCATCTCCACCAACA T A TNIP1 Ensembl:ENSG00000145901 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151035031..151036927 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 11 stomach Human_RBP_ID_944715,Human_RBP_ID_3967562,Human_RBP_ID_22680899,Human_RBP_ID_26351641 Human_Splice_Rec_711274,Human_Splice_Rec_711306,Human_Splice_Rec_711338,Human_Splice_Rec_711346,Human_Splice_Rec_711372,Human_Splice_Rec_711404,Human_Splice_Rec_711436,Human_Splice_Rec_711476,Human_Splice_Rec_711504,Human_Splice_Rec_711536,Human_Splice_Rec_711568,Human_Splice_Rec_711598,Human_Splice_Rec_711624 Human_miRNA_ID_2146214,Human_miRNA_ID_2987644,Human_miRNA_ID_3021336 RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_235529,RMVar_hsa_circ_370270,RMVar_hsa_circ_71409,RMVar_hsa_circ_361478 114734 RMVar_ID_114734 Human_SNP_ID_860135650 m1A Human chr5 - 138166680 138166680 138166680 CCCGGCTTTTAGAAGCTGGTCCTACACAGTTCACCACACCTCTTGCTTCCTTCACTACTGTTGCC CCCGGCTTTTAGAAGCTGGTCCTACACAGTTCCCCACACCTCTTGCTTCCTTCACTACTGTTGCC T G BRD8 Ensembl:ENSG00000112983 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138166548..138166699 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_3758677,Human_RBP_ID_15311408,Human_RBP_ID_23039206,Human_RBP_ID_25937063,Human_RBP_ID_27074328 Human_Splice_Rec_695394,Human_Splice_Rec_695578,Human_Splice_Rec_695618,Human_Splice_Rec_695694 Human_miRNA_ID_117384,Human_miRNA_ID_831372,Human_miRNA_ID_1969939 RMVar_hsa_circ_81575,RMVar_hsa_circ_234753,RMVar_hsa_circ_234755,RMVar_hsa_circ_364886,RMVar_hsa_circ_102696,RMVar_hsa_circ_93708,RMVar_hsa_circ_35412,RMVar_hsa_circ_234757 114735 RMVar_ID_114735 Human_SNP_ID_860141326 m1A Human chr5 - 150447708 150447708 150447708 CTCAGAAATGGCACCTCGAAAGGGGAAGGAAAAGAAGGAAGAACAGGTCATCAGCCTCGGACCTC CTCAGAAATGGCACCTCGAAAGGGGAAGGAAAGGAAGGAAGAACAGGTCATCAGCCTCGGACCTC T C RPS14 Ensembl:ENSG00000164587 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney Human_RBP_ID_76527,Human_RBP_ID_635200,Human_RBP_ID_839220,Human_RBP_ID_945434,Human_RBP_ID_1648303,Human_RBP_ID_1990509,Human_RBP_ID_2909641,Human_RBP_ID_3762808,Human_RBP_ID_3968364,Human_RBP_ID_4817516,Human_RBP_ID_5121719,Human_RBP_ID_8267426,Human_RBP_ID_8607574,Human_RBP_ID_15352036,Human_RBP_ID_17662611,Human_RBP_ID_18195263,Human_RBP_ID_18448365,Human_RBP_ID_18836411,Human_RBP_ID_21138344,Human_RBP_ID_22460256,Human_RBP_ID_22827634,Human_RBP_ID_23051336,Human_RBP_ID_24504652,Human_RBP_ID_25938773,Human_RBP_ID_26351634 Human_Splice_Rec_710678,Human_Splice_Rec_710686,Human_Splice_Rec_710694,Human_Splice_Rec_710710,Human_Splice_Rec_710722 Human_miRNA_ID_1978710 RMVar_hsa_circ_89631,RMVar_hsa_circ_105764,RMVar_hsa_circ_235464,RMVar_hsa_circ_235463,RMVar_hsa_circ_337480,RMVar_hsa_circ_235469,RMVar_hsa_circ_115038 114736 RMVar_ID_114736 Human_SNP_ID_860201216 m1A Human chr5 - 90409698 90409698 90409698 GGGCGTCTTGCTGCCTTGGGTAGGGGGTTAAAATCGTTCTTGAGAGGAACGTCTCTGTGCGAAGA GGGCGTCTTGCTGCCTTGGGTAGGGGGTTAAAGTCGTTCTTGAGAGGAACGTCTCTGTGCGAAGA T C CETN3 Ensembl:ENSG00000153140 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:90409596..90409750 26863196 MeRIP-seq:(Medium) rs766130292 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 7 lung Human_RBP_ID_4845836,Human_RBP_ID_8943888,Human_RBP_ID_24121224,Human_RBP_ID_27826554 Human_Splice_Rec_671541,Human_Splice_Rec_671549,Human_Splice_Rec_671559,Human_Splice_Rec_671575,Human_Splice_Rec_671581 RMVar_hsa_circ_3679 114737 RMVar_ID_114737 Human_SNP_ID_860220409 m1A Human chr5 + 150649761 150649761 150649761 CCCGCCGCCAGTCACGGATGGAGAAATATGTCATCGAGTCTTCAAGCCACACGCCAGAGCTGGCC CCCGCCGCCAGTCACGGATGGAGAAATATGTCGTCGAGTCTTCAAGCCACACGCCAGAGCTGGCC A G SYNPO Ensembl:ENSG00000171992 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150649710..150650263 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 4 haematopoietic and lymphoid tissue 114738 RMVar_ID_114738 Human_SNP_ID_860233747 m1A Human chr5 + 154793698 154793698 154793698 CGCCCCACTCGCCCACCGGAGCCTAGACACATACCTGCCAATCGCGGAGAGATCAAAGGTATGCA CGCCCCACTCGCCCACCGGAGCCTAGACACATCCCTGCCAATCGCGGAGAGATCAAAGGTATGCA A C LARP1 Ensembl:ENSG00000155506 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:154793651..154793801 26863196 MeRIP-seq:(Medium) rs766970973 Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus Human_RBP_ID_76076,Human_RBP_ID_1040110,Human_RBP_ID_8887049,Human_RBP_ID_9305290,Human_RBP_ID_9398593,Human_RBP_ID_17298998,Human_RBP_ID_26352816 Human_Splice_Rec_713479,Human_Splice_Rec_713515,Human_Splice_Rec_713551,Human_Splice_Rec_713563,Human_Splice_Rec_713573,Human_Splice_Rec_713593,Human_Splice_Rec_713605 RMVar_hsa_circ_65232,RMVar_hsa_circ_81554,RMVar_hsa_circ_110814,RMVar_hsa_circ_101061,RMVar_hsa_circ_79212,RMVar_hsa_circ_235696,RMVar_hsa_circ_235697,RMVar_hsa_circ_235698,RMVar_hsa_circ_235700,RMVar_hsa_circ_235702,RMVar_hsa_circ_235707,RMVar_hsa_circ_299458,RMVar_hsa_circ_340952,RMVar_hsa_circ_341945,RMVar_hsa_circ_348062,RMVar_hsa_circ_336714,RMVar_hsa_circ_301566,RMVar_hsa_circ_287674,RMVar_hsa_circ_275640,RMVar_hsa_circ_235705,RMVar_hsa_circ_235706,RMVar_hsa_circ_235704,RMVar_hsa_circ_119899,RMVar_hsa_circ_235708,RMVar_hsa_circ_269201,RMVar_hsa_circ_373885,RMVar_hsa_circ_311601,RMVar_hsa_circ_235709,RMVar_hsa_circ_235710,RMVar_hsa_circ_320153,RMVar_hsa_circ_37647,RMVar_hsa_circ_235712 114739 RMVar_ID_114739 Human_SNP_ID_860240560 m1A Human chr5 + 17204086 17204086 17204086 CTAGCTAATGCTGCATTTCTCTGCTTCCTGTCACAATCAATAAAACTTCTGGAAAGTTTCGTCTG CTAGCTAATGCTGCATTTCTCTGCTTCCTGTCGCAATCAATAAAACTTCTGGAAAGTTTCGTCTG A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17203855..17204397 26863196 MeRIP-seq:(Medium) rs57900343 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114740 RMVar_ID_114740 Human_SNP_ID_860260278 m1A Human chr5 + 34005759 34005759 34005759 AGTGTAGACTAAATTTTTTTTCAACATACCTGACAAAGCCAAATAGTTGATATCGTGGCCAGCTA AGTGTAGACTAAATTTTTTTTCAACATACCTGGCAAAGCCAAATAGTTGATATCGTGGCCAGCTA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:34004615..34005786 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 114741 RMVar_ID_114741 Human_SNP_ID_860288595 m1A Human chr5 + 127553001 127553001 127553001 CGTGGAAGCCTTTTCCCCTCAAATAATATATTATATCATTTTTGGACTTATATAAATGATAATTA CGTGGAAGCCTTTTCCCCTCAAATAATATATTTTATCATTTTTGGACTTATATAAATGATAATTA A T PRRC1 Ensembl:ENSG00000164244 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs496004 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17526776,Human_RBP_ID_18037362,Human_RBP_ID_27733693 Human_miRNA_ID_1088615,Human_miRNA_ID_1119897,Human_miRNA_ID_1127029 GWAS_ID_13993,GWAS_ID_13994,GWAS_ID_13995,GWAS_ID_13996,GWAS_ID_13997,GWAS_ID_13998,GWAS_ID_13999,GWAS_ID_14000,GWAS_ID_14001,GWAS_ID_14002,GWAS_ID_14003,GWAS_ID_14004,GWAS_ID_14005,GWAS_ID_14006,GWAS_ID_14007,GWAS_ID_14008,GWAS_ID_14009,GWAS_ID_14010,GWAS_ID_14011,GWAS_ID_14012,GWAS_ID_14013,GWAS_ID_14014,GWAS_ID_14015,GWAS_ID_14016,GWAS_ID_14017,GWAS_ID_14018,GWAS_ID_14019,GWAS_ID_14020,GWAS_ID_14021,GWAS_ID_14022,GWAS_ID_14023,GWAS_ID_14024,GWAS_ID_14025,GWAS_ID_14026,GWAS_ID_14027,GWAS_ID_14028,GWAS_ID_14029,GWAS_ID_14030,GWAS_ID_14031,GWAS_ID_14032,GWAS_ID_14033,GWAS_ID_14034,GWAS_ID_14035,GWAS_ID_14036,GWAS_ID_14037,GWAS_ID_14038,GWAS_ID_14039,GWAS_ID_14040,GWAS_ID_14041,GWAS_ID_14042,GWAS_ID_14043,GWAS_ID_14044,GWAS_ID_14045,GWAS_ID_14046,GWAS_ID_14047,GWAS_ID_14048,GWAS_ID_14049,GWAS_ID_14050,GWAS_ID_14051,GWAS_ID_14052,GWAS_ID_14053,GWAS_ID_14054,GWAS_ID_14055,GWAS_ID_14056,GWAS_ID_14057,GWAS_ID_14058,GWAS_ID_14059,GWAS_ID_14060,GWAS_ID_14061,GWAS_ID_14062,GWAS_ID_14063,GWAS_ID_14064,GWAS_ID_14065,GWAS_ID_14066,GWAS_ID_14067,GWAS_ID_14068 114742 RMVar_ID_114742 Human_SNP_ID_860298117 m1A Human chr5 + 151804045 151804045 151804045 AATGAGAGGCCCTCCCCGTGGAGGCATGGTGCAGAAACCAGGATTTGGAGTGGGAAGGGGGCTTG AATGAGAGGCCCTCCCCGTGGAGGCATGGTGCTGAAACCAGGATTTGGAGTGGGAAGGGGGCTTG A T G3BP1 Ensembl:ENSG00000145907 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:151803901..151804200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus Human_RBP_ID_250189,Human_RBP_ID_839063,Human_RBP_ID_946781,Human_RBP_ID_1990734,Human_RBP_ID_4851748,Human_RBP_ID_7407040,Human_RBP_ID_8607905,Human_RBP_ID_9354548,Human_RBP_ID_17663000,Human_RBP_ID_22297441,Human_RBP_ID_22459357,Human_RBP_ID_24091707,Human_RBP_ID_24385664,Human_RBP_ID_25873576 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 114743 RMVar_ID_114743 Human_SNP_ID_860309641 m1A Human chr5 + 178163874 178163874 178163874 AAGGAAGGGAGGGAAAAGAGAAAAAAGAAAAGAAAGGAAGACCAATGTAGAGGGTGAGGCAGGGC AAGGAAGGGAGGGAAAAGAGAAAAAAGAAAAGGAAGGAAGACCAATGTAGAGGGTGAGGCAGGGC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:178163761..178163985 26863196 MeRIP-seq:(Medium) rs1312149811 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 114744 RMVar_ID_114744 Human_SNP_ID_860346249 m1A Human chr5 - 150124339 150124339 150124339 ATTTTCCTCAGCCACAGCCCGCAGCAGTGAGAAGCAAGCCCTTATGTCGGAGCTGAAGATCATGA ATTTTCCTCAGCCACAGCCCGCAGCAGTGAGACGCAAGCCCTTATGTCGGAGCTGAAGATCATGA T G PDGFRB Ensembl:ENSG00000113721 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:150124192..150124350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_Splice_Rec_709358,Human_Splice_Rec_709359,Human_Splice_Rec_709402,Human_Splice_Rec_709403 RMVar_hsa_circ_128012,RMVar_hsa_circ_85014,RMVar_hsa_circ_26715,RMVar_hsa_circ_94718,RMVar_hsa_circ_235433,RMVar_hsa_circ_235434,RMVar_hsa_circ_235436,RMVar_hsa_circ_90764,RMVar_hsa_circ_235435,RMVar_hsa_circ_44908 114745 RMVar_ID_114745 Human_SNP_ID_860346355 m1A Human chr5 - 146447410 146447410 146447410 GAGCAGAGATGTGAAGGAGGGCAGCGTTCCTTACCTGAGCTCCCCCGGGTTGAATCGTTCACTCT GAGCAGAGATGTGAAGGAGGGCAGCGTTCCTTGCCTGAGCTCCCCCGGGTTGAATCGTTCACTCT T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:146447326..146447482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 114746 RMVar_ID_114746 Human_SNP_ID_860354302 m1A Human chr5 + 179806706 179806706 179806706 GCGGCGGCAGGGGCCCCGGCCCCGGGTCGGGGAGGGGCGGGGGGCCCGGGGCCGGGCGGGGACCG GCGGCGGCAGGGGCCCCGGCCCCGGGTCGGGGGGGGGCGGGGGGCCCGGGGCCGGGCGGGGACCG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:179806606..179806827 26863196 MeRIP-seq:(Medium) rs906425616 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5214733,Human_RBP_ID_8213335 114747 RMVar_ID_114747 Human_SNP_ID_860393704 m1A Human chr5 + 176379262 176379262 176379262 GTAATCTCAGCTCGCTGCAATCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCATAAGCCTCCCG GTAATCTCAGCTCGCTGCAATCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCATAAGCCTCCCG A T ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114748 RMVar_ID_114748 Human_SNP_ID_860398173 m1A Human chr5 - 1327143 1327143 1327143 ATGGAATGTGCCTGTAGAGGAGGAGCTGGATGAAATGTGTCTGTAGAGGAGGAGCTGGATGGAAT ATGGAATGTGCCTGTAGAGGAGGAGCTGGATGGAATGTGTCTGTAGAGGAGGAGCTGGATGGAAT T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:1326626..1327262 26863196 MeRIP-seq:(Medium) rs866894228 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_24082783 RMVar_hsa_circ_99023,RMVar_hsa_circ_230031,RMVar_hsa_circ_112689,RMVar_hsa_circ_95048,RMVar_hsa_circ_230032,RMVar_hsa_circ_115470,RMVar_hsa_circ_230036,RMVar_hsa_circ_83307,RMVar_hsa_circ_230037,RMVar_hsa_circ_230038,RMVar_hsa_circ_104525,RMVar_hsa_circ_79677,RMVar_hsa_circ_230041,RMVar_hsa_circ_108983,RMVar_hsa_circ_230042,RMVar_hsa_circ_230043,RMVar_hsa_circ_122771,RMVar_hsa_circ_230044 114749 RMVar_ID_114749 Human_SNP_ID_860467917 m1A Human chr5 + 69320514 69320514 69320514 TCTTCTGTTTCCCAGAGCTGCACGTCTGACTCACTTGATGATCTTGCCACCTTGCTCATGAGCCA TCTTCTGTTTCCCAGAGCTGCACGTCTGACTCCCTTGATGATCTTGCCACCTTGCTCATGAGCCA A C RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:69320464..69320540 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung 114750 RMVar_ID_114750 Human_SNP_ID_860496024 m1A Human chr5 + 119071467 119071467 119071467 TCCAGGCGCCTGTCGCTGCTTCTGCCGTCGCCACCGAAGAGCGGCCGCCGCCCCTGAGGGAAGGA TCCAGGCGCCTGTCGCTGCTTCTGCCGTCGCCCCCGAAGAGCGGCCGCCGCCCCTGAGGGAAGGA A C DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:119071461..119071575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_4845886,Human_RBP_ID_9335288 RMVar_hsa_circ_93745,RMVar_hsa_circ_233916 114751 RMVar_ID_114751 Human_SNP_ID_860527554 m1A Human chr5 - 893072 893072 893072 CAGGTCCGGCTCACCTGCTGCCGCGCTGATGCACCTCCACGTGGACCGTTGGCGACTCGGCCACA CAGGTCCGGCTCACCTGCTGCCGCGCTGATGCCCCTCCACGTGGACCGTTGGCGACTCGGCCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr5:892851..893100;chr5:892851..893348;chr5:892876..893100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114752 RMVar_ID_114752 Human_SNP_ID_860555557 m1A Human chr5 - 93585025 93585025 93585025 GCGGATCTCGCCAGCTGCTAACTACCATTGCCATATCTTTGGGCCCGGGGAGCGCTGGGGGGAGC GCGGATCTCGCCAGCTGCTAACTACCATTGCCGTATCTTTGGGCCCGGGGAGCGCTGGGGGGAGC T C NR2F1-AS1 Ensembl:ENSG00000237187 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:93584976..93585126 26863196 MeRIP-seq:(Medium) rs886041216 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114753 RMVar_ID_114753 Human_SNP_ID_860560065 m1A Human chr5 - 251069 251069 251069 CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCATAGAGCTTGCTGATTTTCCCACAACCTTCTTG CGGTCGAACGTCTTCAGGTGCTTTAGGTCTCCGTAGAGCTTGCTGATTTTCCCACAACCTTCTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:251026..251405 32194978 MeRIP-seq:(Medium) rs747249998 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Clinvar_Rec_149,Clinvar_Rec_150 114754 RMVar_ID_114754 Human_SNP_ID_860567536 m1A Human chr5 + 146482900 146482900 146482900 GCAACAGCCTTTTTCTTGGCTAATCTTATCATATTTAACTAAATGCCATTTTACTGTCCTTTTAA GCAACAGCCTTTTTCTTGGCTAATCTTATCATGTTTAACTAAATGCCATTTTACTGTCCTTTTAA A G TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3756502 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_17629963,Human_RBP_ID_24433690,Human_RBP_ID_25869724 GWAS_ID_15325 RMVar_hsa_circ_29859,RMVar_hsa_circ_101453,RMVar_hsa_circ_235300,RMVar_hsa_circ_33041,RMVar_hsa_circ_108113,RMVar_hsa_circ_235305,RMVar_hsa_circ_119316,RMVar_hsa_circ_339815,RMVar_hsa_circ_126626,RMVar_hsa_circ_115636,RMVar_hsa_circ_235307,RMVar_hsa_circ_235308,RMVar_hsa_circ_235309,RMVar_hsa_circ_50450,RMVar_hsa_circ_49040,RMVar_hsa_circ_371813,RMVar_hsa_circ_235310,RMVar_hsa_circ_73960,RMVar_hsa_circ_354539,RMVar_hsa_circ_52492,RMVar_hsa_circ_235313,RMVar_hsa_circ_305646,RMVar_hsa_circ_17533 114755 RMVar_ID_114755 Human_SNP_ID_860569546 m1A Human chr5 + 139308075 139308075 139308075 GAATCTGGTTATTATGACAGAATGGATTATGAAGATGACAGATTAAGAGATGGAGAAAGGTGTAG GAATCTGGTTATTATGACAGAATGGATTATGACGATGACAGATTAAGAGATGGAGAAAGGTGTAG A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139308026..139308075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_632934,Human_RBP_ID_1645853,Human_RBP_ID_1988134,Human_RBP_ID_2899803,Human_RBP_ID_3759375,Human_RBP_ID_7391849,Human_RBP_ID_8604382,Human_RBP_ID_10184920,Human_RBP_ID_15319458,Human_RBP_ID_18833738,Human_RBP_ID_22511590,Human_RBP_ID_23039659,Human_RBP_ID_24085844,Human_RBP_ID_25861739 Human_miRNA_ID_1543407,Human_miRNA_ID_1543408,Human_miRNA_ID_1596363,Human_miRNA_ID_1596364 RMVar_hsa_circ_234897,RMVar_hsa_circ_91210,RMVar_hsa_circ_116622,RMVar_hsa_circ_115834,RMVar_hsa_circ_234892,RMVar_hsa_circ_372248,RMVar_hsa_circ_126406,RMVar_hsa_circ_101392,RMVar_hsa_circ_109941,RMVar_hsa_circ_79033,RMVar_hsa_circ_85144,RMVar_hsa_circ_89228,RMVar_hsa_circ_234901,RMVar_hsa_circ_234903,RMVar_hsa_circ_234904,RMVar_hsa_circ_234902,RMVar_hsa_circ_234899,RMVar_hsa_circ_234900,RMVar_hsa_circ_234898,RMVar_hsa_circ_122270,RMVar_hsa_circ_234896,RMVar_hsa_circ_234912,RMVar_hsa_circ_66099,RMVar_hsa_circ_118135,RMVar_hsa_circ_302108,RMVar_hsa_circ_234914,RMVar_hsa_circ_114464,RMVar_hsa_circ_234915,RMVar_hsa_circ_62131,RMVar_hsa_circ_234916 114756 RMVar_ID_114756 Human_SNP_ID_860570500 m1A Human chr5 + 180291999 180291994 180292000 CGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCAGTGGGTGTGAGGGGCGCCGGGGCGCTGCGACC CGCCCCGCCGCCGCCGCCGCCGCCGCCG______TGGGTGTGAGGGGCGCCGGGGCGCTGCGACC GCCGCAG G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,untreat control chr5:180291908..180292050;chr5:180291899..180292035 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 29..34 33 LMS 1 - 114757 RMVar_ID_114757 Human_SNP_ID_860574233 m1A Human chr5 - 1341826 1341826 1341826 CAGTTAATGTTTCTGTACCAAAGAAAACGAGAAACAATGGGACGCTGTATGCCTACATCTTCCTC CAGTTAATGTTTCTGTACCAAAGAAAACGAGAGACAATGGGACGCTGTATGCCTACATCTTCCTC T C CLPTM1L Ensembl:ENSG00000049656 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:1341776..1341825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_631880,Human_RBP_ID_1987084,Human_RBP_ID_24503441 Human_Splice_Rec_632434,Human_Splice_Rec_632504 RMVar_hsa_circ_98576,RMVar_hsa_circ_71711,RMVar_hsa_circ_230049,RMVar_hsa_circ_25216 114758 RMVar_ID_114758 Human_SNP_ID_860588465 m1A Human chr5 + 36606689 36606689 36606689 ATTGTTGCTCCGTTGTACCTGCTGGGGAATTCACCTCGTTACTGCTTGATATCTTCCACCCCTTA ATTGTTGCTCCGTTGTACCTGCTGGGGAATTCGCCTCGTTACTGCTTGATATCTTCCACCCCTTA A G SLC1A3 Ensembl:ENSG00000079215 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:36606639..36606770 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_18448771 Human_Splice_Rec_643827,Human_Splice_Rec_643841,Human_Splice_Rec_643857,Human_Splice_Rec_643863,Human_Splice_Rec_643881,Human_Splice_Rec_643885,Human_Splice_Rec_643887,Human_Splice_Rec_643891 Human_miRNA_ID_2068370 RMVar_hsa_circ_230824,RMVar_hsa_circ_87918 114759 RMVar_ID_114759 Human_SNP_ID_860592079 m1A Human chr5 - 177098006 177098006 177098006 CGTCAAGACGCTGGGGCAGCAGCAGCAGGGGGAGGTGTGGGGAAAGGGGGTTCAGAGGCCCAGAA CGTCAAGACGCTGGGGCAGCAGCAGCAGGGGGGGGTGTGGGGAAAGGGGGTTCAGAGGCCCAGAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177097959..177098052 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114760 RMVar_ID_114760 Human_SNP_ID_860637576 m1A Human chr5 + 146447369 146447369 146447369 GCGGCCCTCTGTAATGGCGGAGCGTGGCGGGGACGGGGGCGAGAGTGAACGATTCAACCCGGGGG GCGGCCCTCTGTAATGGCGGAGCGTGGCGGGGGCGGGGGCGAGAGTGAACGATTCAACCCGGGGG A G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146447326..146447490 26863196 MeRIP-seq:(Medium) rs1039013282 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_12519,Human_RBP_ID_74816,Human_RBP_ID_249968,Human_RBP_ID_787674,Human_RBP_ID_8885994,Human_RBP_ID_9398494,Human_RBP_ID_18425029,Human_RBP_ID_18448303,Human_RBP_ID_19016042,Human_RBP_ID_27825983 Human_Splice_Rec_705721,Human_Splice_Rec_705741,Human_Splice_Rec_705783,Human_Splice_Rec_705823 RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300 114761 RMVar_ID_114761 Human_SNP_ID_860654453 m1A Human chr5 + 34796004 34796004 34796004 ATGCCTCAGGGTCATGATTACACATGGTGTGGATGTGACAGCCCAAGATACTACCGGTATGTGGT ATGCCTCAGGGTCATGATTACACATGGTGTGGGTGTGACAGCCCAAGATACTACCGGTATGTGGT A G RAI14 Ensembl:ENSG00000039560 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:34795953..34808637 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_73475,Human_RBP_ID_24104125 Human_Splice_Rec_641650,Human_Splice_Rec_641651,Human_Splice_Rec_641686,Human_Splice_Rec_641687,Human_Splice_Rec_641698,Human_Splice_Rec_641699,Human_Splice_Rec_641716,Human_Splice_Rec_641717,Human_Splice_Rec_641726,Human_Splice_Rec_641727,Human_Splice_Rec_641758,Human_Splice_Rec_641759,Human_Splice_Rec_641792,Human_Splice_Rec_641793,Human_Splice_Rec_641804,Human_Splice_Rec_641805,Human_Splice_Rec_641832,Human_Splice_Rec_641833,Human_Splice_Rec_641872,Human_Splice_Rec_641873,Human_Splice_Rec_641882,Human_Splice_Rec_641883,Human_Splice_Rec_641892,Human_Splice_Rec_641893,Human_Splice_Rec_641902,Human_Splice_Rec_641903,Human_Splice_Rec_641940,Human_Splice_Rec_641941,Human_Splice_Rec_641954,Human_Splice_Rec_641960,Human_Splice_Rec_641961,Human_Splice_Rec_641972,Human_Splice_Rec_641973,Human_Splice_Rec_641984,Human_Splice_Rec_641985,Human_Splice_Rec_642016,Human_Splice_Rec_642022,Human_Splice_Rec_642023,Human_Splice_Rec_642030,Human_Splice_Rec_642031,Human_Splice_Rec_642042,Human_Splice_Rec_642043 RMVar_hsa_circ_8809,RMVar_hsa_circ_19042,RMVar_hsa_circ_87405,RMVar_hsa_circ_230761,RMVar_hsa_circ_319683,RMVar_hsa_circ_26895,RMVar_hsa_circ_230763,RMVar_hsa_circ_57779,RMVar_hsa_circ_84569,RMVar_hsa_circ_127467,RMVar_hsa_circ_230765,RMVar_hsa_circ_230764,RMVar_hsa_circ_295910,RMVar_hsa_circ_349190,RMVar_hsa_circ_282461,RMVar_hsa_circ_107300,RMVar_hsa_circ_230766,RMVar_hsa_circ_230768,RMVar_hsa_circ_230770,RMVar_hsa_circ_230771,RMVar_hsa_circ_230769,RMVar_hsa_circ_230767 114762 RMVar_ID_114762 Human_SNP_ID_860662617 m1A Human chr5 + 150390011 150390011 150390011 AGTCGGATATCAGATGGCAAGAAACAGGAGGGACCAGCCACTCAGGTACCTGGTGGGCAAGGGAG AGTCGGATATCAGATGGCAAGAAACAGGAGGGCCCAGCCACTCAGGTACCTGGTGGGCAAGGGAG A C TCOF1 Ensembl:ENSG00000070814 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150389961..150391582 32194978 MeRIP-seq:(Medium) rs199924881 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_9307182,Human_RBP_ID_15351306,Human_RBP_ID_22364778,Human_RBP_ID_26351620,Human_RBP_ID_27826032 Human_Splice_Rec_709969,Human_Splice_Rec_710013,Human_Splice_Rec_710061,Human_Splice_Rec_710109,Human_Splice_Rec_710159,Human_Splice_Rec_710257,Human_Splice_Rec_710337,Human_Splice_Rec_710385,Human_Splice_Rec_710435,Human_Splice_Rec_710517,Human_Splice_Rec_710545,Human_Splice_Rec_710559,Human_Splice_Rec_710561 RMVar_hsa_circ_83662,RMVar_hsa_circ_235454 114763 RMVar_ID_114763 Human_SNP_ID_860663175 m1A Human chr5 + 150052521 150052521 150052521 TTCCGTGGGGCCTGCGGTGTGGGTCAGGGTGGAGGTCCTGGGTGGGCTAAGGCGTGAGCCCCAGC TTCCGTGGGGCCTGCGGTGTGGGTCAGGGTGGCGGTCCTGGGTGGGCTAAGGCGTGAGCCCCAGC A C HMGXB3 Ensembl:ENSG00000113716 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:150052396..150052595 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_3968351,Human_RBP_ID_5151164,Human_RBP_ID_5532094,Human_RBP_ID_7405489,Human_RBP_ID_9354543,Human_RBP_ID_26529401,Human_RBP_ID_26771678 114764 RMVar_ID_114764 Human_SNP_ID_860682701 m1A Human chr5 - 151786555 151786555 151786555 TCAAATATGTCCAAACCTGAAGGATCAAACACAGGGGAAAAGACCGAATCATTTAGCTGAAACCA TCAAATATGTCCAAACCTGAAGGATCAAACACGGGGGAAAAGACCGAATCATTTAGCTGAAACCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:151786551..151786725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114765 RMVar_ID_114765 Human_SNP_ID_860693645 m1A Human chr5 + 179623607 179623607 179623607 CTCGCAAAAACGGTACCCACCGTGGTCGCTGAACTGCAAGCGAGGACCCACCGCGACTCACCTAG CTCGCAAAAACGGTACCCACCGTGGTCGCTGACCTGCAAGCGAGGACCCACCGCGACTCACCTAG A C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr5:179623551..179623675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114766 RMVar_ID_114766 Human_SNP_ID_860740110 m1A Human chr5 - 31526320 31526320 31526320 CCAGTGCTAATAACAGCAGTAGTCCTCATTTCAGACATCTCCCTCCATACCCACTCCCAAAGGCT CCAGTGCTAATAACAGCAGTAGTCCTCATTTCGGACATCTCCCTCCATACCCACTCCCAAAGGCT T C DROSHA Ensembl:ENSG00000113360 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:31526276..31526782 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_74341,Human_RBP_ID_1069477,Human_RBP_ID_2924464,Human_RBP_ID_5133946,Human_RBP_ID_9398998,Human_RBP_ID_15422417,Human_RBP_ID_17090185,Human_RBP_ID_18841124,Human_RBP_ID_22300525,Human_RBP_ID_27515387 Human_miRNA_ID_2978695 RMVar_hsa_circ_110996,RMVar_hsa_circ_230645 114767 RMVar_ID_114767 Human_SNP_ID_860747063 m1A Human chr5 - 14797980 14797980 14797980 CCCGTTATATGCCCCAGAACCCTTGTATCATCACAACAAAGACTCCTTCCAGTGATATTCTTGTC CCCGTTATATGCCCCAGAACCCTTGTATCATCGCAACAAAGACTCCTTCCAGTGATATTCTTGTC T C ANKH,RBBP4P1 Ensembl:ENSG00000154122,Ensembl:ENSG00000249485 Protein coding,Pseudogene intron,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1209776064 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 114768 RMVar_ID_114768 Human_SNP_ID_860755545 m1A Human chr5 + 109193028 109193028 109193028 TAAAATGACCCATAGCCAACAATAAATGCAATAACAATAAAGGAAACTAACCCTCACAAAGGGTT TAAAATGACCCATAGCCAACAATAAATGCAATGACAATAAAGGAAACTAACCCTCACAAAGGGTT A G FER Ensembl:ENSG00000151422 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11738705 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma,liver hepatocellular_carcinoma 2 liver,prostate Human_RBP_ID_17526043 GWAS_ID_9308,GWAS_ID_9309,GWAS_ID_9310 114769 RMVar_ID_114769 Human_SNP_ID_860761487 m1A Human chr5 + 17217085 17217085 17217085 GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGAGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT GGAGAGAGAGAGAGAGAGTGAGAGAGAGAGAGTGAGAGAGAGAGTGAGTGAGAGAGTGAGAGAGT A T BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17217080..17217282 26863196 MeRIP-seq:(Medium) rs1158852455 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114770 RMVar_ID_114770 Human_SNP_ID_860763123 m1A Human chr5 + 1335143 1335143 1335143 GCCCCAGTGAGACCTTGTCGTAGGACACGGTGAGGGGCAGCTCGGTGGTGGAGCGGTTTATGACC GCCCCAGTGAGACCTTGTCGTAGGACACGGTGGGGGGCAGCTCGGTGGTGGAGCGGTTTATGACC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1335095..1335218 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney 114771 RMVar_ID_114771 Human_SNP_ID_860767105 m1A Human chr5 - 224462 224462 224462 AGGAAACAGCTTGGTAACACATGCTGTATTAAACCCTGCCTCAGAAAGGCCAAATGCAGCTCGCA AGGAAACAGCTTGGTAACACATGCTGTATTAACCCCTGCCTCAGAAAGGCCAAATGCAGCTCGCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:224351..224577 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114772 RMVar_ID_114772 Human_SNP_ID_860772638 m1A Human chr5 - 14711214 14711214 14711214 CGACAGAGGAGGTGACAGACATCGTGGAAATGAGAGAGGAGAATGAATAAGGCACGGGACGCCAT CGACAGAGGAGGTGACAGACATCGTGGAAATGTGAGAGGAGAATGAATAAGGCACGGGACGCCAT T A ANKH Ensembl:ENSG00000154122 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:14711164..14711325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_1647691,Human_RBP_ID_2907558,Human_RBP_ID_7402998,Human_RBP_ID_27512656 Human_Splice_Rec_636700,Human_Splice_Rec_636706 114773 RMVar_ID_114773 Human_SNP_ID_860783768 m1A Human chr5 + 55307862 55307858 55307862 GGTCGGAAAGGAAAGGAAAGAAAAGCAGGAAAAAAAAAAAAAGTCAGGGGAACATTTTTGTCGGC GGTCGGAAAGGAAAGGAAAGAAAAGCAGG____AAAAAAAAAGTCAGGGGAACATTTTTGTCGGC GAAAA G NONHSAG040397.2 RNACentral:URS00009B204C lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:55307812..55307922 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 30..33 33 COAD 1 - RMVar_hsa_circ_90256,RMVar_hsa_circ_113697,RMVar_hsa_circ_106571,RMVar_hsa_circ_231392,RMVar_hsa_circ_231393,RMVar_hsa_circ_231394 114774 RMVar_ID_114774 Human_SNP_ID_860809453 m1A Human chr5 + 17315932 17315932 17315932 CAGTGGCACAATCTTGGCTCACTGCAACCTCCACCTCCTGAGTTTAAGTGATTTTCCTGCCTCAG CAGTGGCACAATCTTGGCTCACTGCAACCTCCTCCTCCTGAGTTTAAGTGATTTTCCTGCCTCAG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:17315922..17316001 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114775 RMVar_ID_114775 Human_SNP_ID_860811915 m1A Human chr5 - 179833127 179833127 179833127 GCTGGGGTCAGAGCAGCAGCTGCTTGGCTGTGAGCTGCTCTTCTCCTCTGTGCTGGAACTCTCTG GCTGGGGTCAGAGCAGCAGCTGCTTGGCTGTGCGCTGCTCTTCTCCTCTGTGCTGGAACTCTCTG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:179833076..179833287 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 114776 RMVar_ID_114776 Human_SNP_ID_860813668 m1A Human chr5 + 94569445 94569445 94569445 CCCCACAAACCCCATTACTAAAACCACACTTAACAAAAATAAAGCATATGTCATTATTCTCGCAC CCCCACAAACCCCATTACTAAAACCACACTTAGCAAAAATAAAGCATATGTCATTATTCTCGCAC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:94569345..94569525 26863410 MeRIP-seq:(Medium) rs1366514748 Functional Loss SNV ICGC 33..33 33 RECA 1 - 114777 RMVar_ID_114777 Human_SNP_ID_860817989 m1A Human chr5 + 163513993 163513993 163513993 GATGGAGAAAAGGCTGTCCTGGAGAACAATCTAGGTAAGACCTAATCTATTTAGCCCCTGATTGT GATGGAGAAAAGGCTGTCCTGGAGAACAATCTGGGTAAGACCTAATCTATTTAGCCCCTGATTGT A G MAT2B Ensembl:ENSG00000038274 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11546512 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_Splice_Rec_717787,Human_Splice_Rec_717799,Human_Splice_Rec_717809,Human_Splice_Rec_717817,Human_Splice_Rec_717827,Human_Splice_Rec_717837 RMVar_hsa_circ_235952,RMVar_hsa_circ_286323,RMVar_hsa_circ_297000,RMVar_hsa_circ_360314,RMVar_hsa_circ_235953,RMVar_hsa_circ_59204,RMVar_hsa_circ_280753,RMVar_hsa_circ_349278,RMVar_hsa_circ_235954 114778 RMVar_ID_114778 Human_SNP_ID_860818224 m1A Human chr5 + 64769047 64769047 64769047 GTGATATTGACAAACTGAAGCTTTCCTGCACCACTGGACTTAAGGAAGAGTGTACTCGTAGGCGG GTGATATTGACAAACTGAAGCTTTCCTGCACCTCTGGACTTAAGGAAGAGTGTACTCGTAGGCGG A T CWC27 Ensembl:ENSG00000153015 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr5:64768959..64769079 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_644432,Human_RBP_ID_1656223,Human_RBP_ID_1997534,Human_RBP_ID_4845739,Human_RBP_ID_5427429,Human_RBP_ID_5476829,Human_RBP_ID_5611154,Human_RBP_ID_9178898 114779 RMVar_ID_114779 Human_SNP_ID_860826436 m1A Human chr5 - 141319198 141319198 141319198 AAGGAACCAATCAGCTGGTTATGGGAATTCAGAAGCAGATTGACAACATGAAAGGCAAGCTCCAA AAGGAACCAATCAGCTGGTTATGGGAATTCAGTAGCAGATTGACAACATGAAAGGCAAGCTCCAA T A TAF7 Ensembl:ENSG00000178913 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:141319148..141319427 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_78683,Human_RBP_ID_1646567,Human_RBP_ID_1988877,Human_RBP_ID_3760246,Human_RBP_ID_7395342,Human_RBP_ID_8885417,Human_RBP_ID_9398413,Human_RBP_ID_15328815,Human_RBP_ID_17527849,Human_RBP_ID_21214113,Human_RBP_ID_22099732,Human_RBP_ID_22511664,Human_RBP_ID_24548209,Human_RBP_ID_26351491,Human_RBP_ID_27825951 RMVar_hsa_circ_235070 114780 RMVar_ID_114780 Human_SNP_ID_860883009 m1A Human chr5 - 176392620 176392620 176392620 TCTCCAGGCGCTGGGAGGGGGGCCCTCACCCCATCACGCCTCGCTCCCTCCTGGCCCTCTGGTCC TCTCCAGGCGCTGGGAGGGGGGCCCTCACCCCGTCACGCCTCGCTCCCTCCTGGCCCTCTGGTCC T C CLTB Ensembl:ENSG00000175416 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs5866 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_76846,Human_RBP_ID_17663033,Human_RBP_ID_26524920,Human_RBP_ID_26826851 GWAS_ID_7704,GWAS_ID_7705,GWAS_ID_7706,GWAS_ID_7707,GWAS_ID_7708,GWAS_ID_7709,GWAS_ID_7710,GWAS_ID_7711,GWAS_ID_7712,GWAS_ID_7713,GWAS_ID_7714,GWAS_ID_7715,GWAS_ID_7716,GWAS_ID_7717,GWAS_ID_7718 RMVar_hsa_circ_86885,RMVar_hsa_circ_236369 114781 RMVar_ID_114781 Human_SNP_ID_860918547 m1A Human chr5 + 179621375 179621375 179621375 CCTTCTCTGGTGTAGATGAAACGAATACCTTGAGCCCCATTTTGAATTTTGCAGTCTGGAAAGAA CCTTCTCTGGTGTAGATGAAACGAATACCTTGCGCCCCATTTTGAATTTTGCAGTCTGGAAAGAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179621351..179621375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 5 oesophagus 114782 RMVar_ID_114782 Human_SNP_ID_860929025 m1A Human chr5 - 668385 668385 668385 CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGAGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT CTCTCTGTGTGCTTGTCGGTACTTCCCTGACGGGGCCCACGCGGACCCCTCTCCAGTGTGCTTGT T C TPPP Ensembl:ENSG00000171368 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:668336..668457;chr5:668334..668423 26863196 MeRIP-seq:(Medium) rs11738955 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 114783 RMVar_ID_114783 Human_SNP_ID_860932627 m1A Human chr5 - 93682884 93682884 93682884 TCAATTATGTGAAGAATTGCTTCCGGATGACTAACCAAGAGGCTATTCAAGATCTCTGGCAGTGG TCAATTATGTGAAGAATTGCTTCCGGATGACTGACCAAGAGGCTATTCAAGATCTCTGGCAGTGG T C NPM1P27,FAM172A Ensembl:ENSG00000249353,Ensembl:ENSG00000113391 Pseudogene,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878979147 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_2950898,Human_RBP_ID_5611378,Human_RBP_ID_7492505,Human_RBP_ID_17416808,Human_RBP_ID_22404067 114784 RMVar_ID_114784 Human_SNP_ID_860934376 m1A Human chr5 + 177490303 177490303 177490303 CCCAAGGCAGCACAGACCTGGCAGACAGCAGTACCACAGGGCAAAGAGGGAAGGCAGTGTCAGAT CCCAAGGCAGCACAGACCTGGCAGACAGCAGTGCCACAGGGCAAAGAGGGAAGGCAGTGTCAGAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:177490301..177490600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 114785 RMVar_ID_114785 Human_SNP_ID_860938892 m1A Human chr5 + 420866 420863 420867 CACGCAGCACGCACAGACCCACGCACGCAGCCACCCACCCACGCAGCACGCACAGACCCACGCAC CACGCAGCACGCACAGACCCACGCACGCAG____CCACCCACGCAGCACGCACAGACCCACGCAC GCCAC G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr5:420767..420955;chr5:420792..420950 26863196 MeRIP-seq:(Medium) rs773356895 Functional Loss DEL ICGC 31..34 33 PBCA 1 - RMVar_hsa_circ_67941,RMVar_hsa_circ_36785,RMVar_hsa_circ_110112,RMVar_hsa_circ_229951,RMVar_hsa_circ_371331,RMVar_hsa_circ_304192,RMVar_hsa_circ_229952,RMVar_hsa_circ_11828 114786 RMVar_ID_114786 Human_SNP_ID_860974784 m1A Human chr5 - 39383045 39383045 39383045 TTTCCGTGACGATCCTTTCACACAGCCAGACCAATCGACACCTTCTTCGTTTGATTCTCTCAAAT TTTCCGTGACGATCCTTTCACACAGCCAGACCCATCGACACCTTCTTCGTTTGATTCTCTCAAAT T G C9,DAB2 Ensembl:ENSG00000113600,Ensembl:ENSG00000153071 Protein coding,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:39382996..39383166 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_18956420,Human_RBP_ID_21088558 Human_miRNA_ID_2767240 RMVar_hsa_circ_33567,RMVar_hsa_circ_116230,RMVar_hsa_circ_113363,RMVar_hsa_circ_231167,RMVar_hsa_circ_231168,RMVar_hsa_circ_9622,RMVar_hsa_circ_64772,RMVar_hsa_circ_265780,RMVar_hsa_circ_347584,RMVar_hsa_circ_231170 114787 RMVar_ID_114787 Human_SNP_ID_860980361 m1A Human chr5 - 160093654 160093654 160093654 TGTGATAAATGTAAAAACAGTGTTGTTGCTGAAAAAAAGGAAATTAGAAAAGGTAGTAGTGCAAC TGTGATAAATGTAAAAACAGTGTTGTTGCTGAGAAAAAGGAAATTAGAAAAGGTAGTAGTGCAAC T C PWWP2A Ensembl:ENSG00000170234 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs56251777 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_24093892 Human_miRNA_ID_2911592 RMVar_hsa_circ_235911,RMVar_hsa_circ_235912,RMVar_hsa_circ_235914,RMVar_hsa_circ_309048,RMVar_hsa_circ_235915,RMVar_hsa_circ_235918,RMVar_hsa_circ_235917,RMVar_hsa_circ_284059,RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_265474,RMVar_hsa_circ_289857 114788 RMVar_ID_114788 Human_SNP_ID_861020213 m1A Human chr5 - 620175 620175 620175 CAACCTTCACCACGGGGTTCAGCCGGAAGTCCACATCCACGAGCTCGGTTAAGGCGTGGAGCCGA CAACCTTCACCACGGGGTTCAGCCGGAAGTCCGCATCCACGAGCTCGGTTAAGGCGTGGAGCCGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:620124..620225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114789 RMVar_ID_114789 Human_SNP_ID_861069108 m1A Human chr5 - 894778 894777 894778 TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAAAGAAGCCAAAACACACATAAATGATCTTAGTTC TTTATGTCTTCTTTCTTTGCAGTGCTAAAAAA_GAAGCCAAAACACACATAAATGATCTTAGTTC CT C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:894776..894850 26863196 MeRIP-seq:(Medium) rs541160921 Functional Loss DEL ICGC 33..33 33 STAD 3 - 114790 RMVar_ID_114790 Human_SNP_ID_861069669 m1A Human chr5 + 85464 85464 85464 TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCAGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA TCAGGGAAGGCTCGATGAGAGGCCGGGTGGTCGGGGAAGCCTCGATGAGAGGCAGCGAGCAGACA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:85406..85566 26863196 MeRIP-seq:(Medium) rs146219474 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114791 RMVar_ID_114791 Human_SNP_ID_861137053 m1A Human chr5 - 72196301 72196301 72196301 ACAGACTCCCTCTTCTCCCTGATGTATGCATCAGCCTCCGCCTTGGCACTTTCCTCATCCTCAGT ACAGACTCCCTCTTCTCCCTGATGTATGCATCTGCCTCCGCCTTGGCACTTTCCTCATCCTCAGT T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr5:72196262..72196408 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 114792 RMVar_ID_114792 Human_SNP_ID_861145704 m1A Human chr5 - 397143 397143 397143 GTCAGGAGCTACGTGGATGGTCAGGGGCTAACATGGATGGTCAGGGGCTAACATGGATGGTCAGG GTCAGGAGCTACGTGGATGGTCAGGGGCTAACGTGGATGGTCAGGGGCTAACATGGATGGTCAGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr5:397003..397179;chr5:396976..397425;chr5:396879..397497 26863196 MeRIP-seq:(Medium) rs1486518648 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,oesophagus adenocarcinoma 4 oesophagus 114793 RMVar_ID_114793 Human_SNP_ID_861163128 m1A Human chr5 - 79427801 79427796 79427801 GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAAAGGAAGGAAGGAAGGAAATGAAGGAAAGGAAGG GAAGGAAGGAAGGAAAAGAAGGAAGGAAGGAA_____GGAAGGAAGGAAATGAAGGAAAGGAAGG CTTCCT C HOMER1 Ensembl:ENSG00000152413 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:79427750..79427838 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..37 33 MALY 1 - Human_RBP_ID_17069733 RMVar_hsa_circ_2953,RMVar_hsa_circ_232719,RMVar_hsa_circ_296199,RMVar_hsa_circ_377588,RMVar_hsa_circ_332660,RMVar_hsa_circ_292846,RMVar_hsa_circ_232720,RMVar_hsa_circ_232717,RMVar_hsa_circ_232718,RMVar_hsa_circ_355131,RMVar_hsa_circ_305547,RMVar_hsa_circ_232721 114794 RMVar_ID_114794 Human_SNP_ID_861167241 m1A Human chr5 + 138783368 138783368 138783368 GAGCTTGTGGCTGCTGTAGAAGATGTTCGAAAACAAGGTAGGTCATTACTGCTTTTTAGGTAAAG GAGCTTGTGGCTGCTGTAGAAGATGTTCGAAAGCAAGGTAGGTCATTACTGCTTTTTAGGTAAAG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138782392..138783375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach Human_RBP_ID_18057331,Human_RBP_ID_19126342,Human_RBP_ID_24085434 Human_Splice_Rec_696879,Human_Splice_Rec_696887,Human_Splice_Rec_696899,Human_Splice_Rec_696911,Human_Splice_Rec_696979,Human_Splice_Rec_697023,Human_Splice_Rec_697033,Human_Splice_Rec_697039,Human_Splice_Rec_697047 RMVar_hsa_circ_22103,RMVar_hsa_circ_351108,RMVar_hsa_circ_360510,RMVar_hsa_circ_368119,RMVar_hsa_circ_285964,RMVar_hsa_circ_297098,RMVar_hsa_circ_281108,RMVar_hsa_circ_61861,RMVar_hsa_circ_127244,RMVar_hsa_circ_234858,RMVar_hsa_circ_234859,RMVar_hsa_circ_109687,RMVar_hsa_circ_234860,RMVar_hsa_circ_234861 114795 RMVar_ID_114795 Human_SNP_ID_861219904 m1A Human chr5 - 72848213 72848213 72848213 GAGGTGCCCCGAAGGAAGTCACGGACAGTGAAACCCGGCGGAACTGCTCCTGGCAGCCCGGCCGC GAGGTGCCCCGAAGGAAGTCACGGACAGTGAATCCCGGCGGAACTGCTCCTGGCAGCCCGGCCGC T A RF00017-4501,lnc-ZNF366-12 RNACentral:URS0000972B66,RNACentral:URS00008BEDA5 SRP RNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:72848202..72848286 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 114796 RMVar_ID_114796 Human_SNP_ID_861230616 m1A Human chr5 - 38845720 38845720 38845720 ACTCGGCGGCCGAGGCTCCGTGCCCCGCGCGCAGCGCTGCTCCTGCCCCGGCCAAGGACGCACGG ACTCGGCGGCCGAGGCTCCGTGCCCCGCGCGCGGCGCTGCTCCTGCCCCGGCCAAGGACGCACGG T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:38845670..38845829 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_5103725,Human_RBP_ID_9399048,Human_RBP_ID_18424942,Human_RBP_ID_23120187 Human_Splice_Rec_645699,Human_Splice_Rec_645715,Human_Splice_Rec_645725,Human_Splice_Rec_645731,Human_Splice_Rec_645735,Human_Splice_Rec_645739 114797 RMVar_ID_114797 Human_SNP_ID_861239164 m1A Human chr5 - 154898652 154898652 154898652 TGACATTTTCTTCACATTTTTATTCATATTATAGCTATTTAGGGGCCACTTGTGCTTATGATGCA TGACATTTTCTTCACATTTTTATTCATATTATGGCTATTTAGGGGCCACTTGTGCTTATGATGCA T C GEMIN5 Ensembl:ENSG00000082516 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:154898606..154899247 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_18043127 RMVar_hsa_circ_101768,RMVar_hsa_circ_119129,RMVar_hsa_circ_107630,RMVar_hsa_circ_111347,RMVar_hsa_circ_235732,RMVar_hsa_circ_14299,RMVar_hsa_circ_235735,RMVar_hsa_circ_235736,RMVar_hsa_circ_235734,RMVar_hsa_circ_51513,RMVar_hsa_circ_49920,RMVar_hsa_circ_346636,RMVar_hsa_circ_235737,RMVar_hsa_circ_377195,RMVar_hsa_circ_371563,RMVar_hsa_circ_235738 114798 RMVar_ID_114798 Human_SNP_ID_861243859 m1A Human chr5 - 176448472 176448472 176448472 GGAGGCATCTGCTGCACCGAGTACTCGCTGCTACCTGAAACTGCAGCAGCTTCTCTGTCTGCTCC GGAGGCATCTGCTGCACCGAGTACTCGCTGCTCCCTGAAACTGCAGCAGCTTCTCTGTCTGCTCC T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:176448376..176448500 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 114799 RMVar_ID_114799 Human_SNP_ID_861244066 m1A Human chr5 + 176381843 176381843 176381843 CTAATGAAGATCTGTCTGAGTCTAATGAATATATTGTACAATTTTTAAAGTCCCCAGTTGTGGGA CTAATGAAGATCTGTCTGAGTCTAATGAATATCTTGTACAATTTTTAAAGTCCCCAGTTGTGGGA A C ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35069679 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_7689,GWAS_ID_7690,GWAS_ID_7691,GWAS_ID_7692,GWAS_ID_7693,GWAS_ID_7694,GWAS_ID_7695,GWAS_ID_7696,GWAS_ID_7697,GWAS_ID_7698,GWAS_ID_7699,GWAS_ID_7700,GWAS_ID_7701,GWAS_ID_7702,GWAS_ID_7703 114800 RMVar_ID_114800 Human_SNP_ID_861261107 m1A Human chr5 + 6632959 6632959 6632959 TCCTCCGGCCGCTGCTGTTGCTGGAGCCGCCGACCCCGCGACCGCCGCCCCATAGCCCACGCGGC TCCTCCGGCCGCTGCTGTTGCTGGAGCCGCCGCCCCCGCGACCGCCGCCCCATAGCCCACGCGGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr5:6632741..6633050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114801 RMVar_ID_114801 Human_SNP_ID_861265140 m1A Human chr5 + 160415299 160415299 160415299 TAACTGCATCTACAACTGTGGCTGACATGGTTATCTGGCCTCCTCTAGGAAAAGAAGTGAAACTT TAACTGCATCTACAACTGTGGCTGACATGGTTGTCTGGCCTCCTCTAGGAAAAGAAGTGAAACTT A G lnc-PTTG1-6 RNACentral:URS00008B6BF6 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:160414408..160417215;chr5:160415126..160415325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 114802 RMVar_ID_114802 Human_SNP_ID_861269924 m1A Human chr5 - 177554532 177554532 177554532 CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC CATATTGGCTGTTGTCCTGTGAGGGGAGCGGTGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC T C FAM193B Ensembl:ENSG00000146067 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177553497..177554575 26863196 MeRIP-seq:(Medium) rs1158273791 Functional Loss SNV ICGC 33..33 33 LICA 1 - 114803 RMVar_ID_114803 Human_SNP_ID_861291208 m1A Human chr5 - 178712441 178712441 178712441 AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCAGCTCTCATTCAACATCAGAGAATGCATACTGG AAAGTATGTGGAAAAGCCTTCAGACAGAGTTCCGCTCTCATTCAACATCAGAGAATGCATACTGG T G AC113348.2,ZNF354A Ensembl:ENSG00000285978,Ensembl:ENSG00000169131 Protein coding,Protein coding intron,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1132338 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,stomach adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 head and neck,stomach,haematopoietic and lymphoid tissue 114804 RMVar_ID_114804 Human_SNP_ID_861293619 m1A Human chr5 - 202799 202799 202799 GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCACGTTTGTCTTTAAATGAAGAAAACACAGTCAG GGTCTGCTGGGTGTCCCTGTGTGAACCACTCCGCGTTTGTCTTTAAATGAAGAAAACACAGTCAG T C CCDC127 Ensembl:ENSG00000164366 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7736361 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114805 RMVar_ID_114805 Human_SNP_ID_861299244 m1A Human chr5 + 179806653 179806653 179806653 CTGCATGGCCCGGGGGACCGGGGCCGGGGCGCAGGGGTCGGAAGGCGGCGGCGGCGGCGGCAGGG CTGCATGGCCCGGGGGACCGGGGCCGGGGCGCGGGGGTCGGAAGGCGGCGGCGGCGGCGGCAGGG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:179806553..179806932 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_27160476 114806 RMVar_ID_114806 Human_SNP_ID_861303465 m1A Human chr5 - 181234461 181234461 181234461 GAGCCGGCGGCGGCGATGGTGATGGCGCGAGGAGCTGGCATCCCCGCTGCCCACGGAGGAACCCC GAGCCGGCGGCGGCGATGGTGATGGCGCGAGGCGCTGGCATCCCCGCTGCCCACGGAGGAACCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:181234412..181234524 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 114807 RMVar_ID_114807 Human_SNP_ID_861307504 m1A Human chr5 + 160414426 160414426 160414426 TTTTAAAGTAGGTCTTTTTGAAGGATCAATATACCATGGCACTGAAGAAATATACTGAGGAATAT TTTTAAAGTAGGTCTTTTTGAAGGATCAATATGCCATGGCACTGAAGAAATATACTGAGGAATAT A G lnc-PTTG1-6 RNACentral:URS00008B6BF6 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:160414376..160414520 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 114808 RMVar_ID_114808 Human_SNP_ID_861311972 m1A Human chr5 - 10254204 10254204 10254204 TGCTAAAAAACACGGAATGGTGGACTCTTACCATTTGGTCCAAGTGATGTTCTCATTGTATTTGC TGCTAAAAAACACGGAATGGTGGACTCTTACCGTTTGGTCCAAGTGATGTTCTCATTGTATTTGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:10254126..10254261 32194978 MeRIP-seq:(Medium) rs775126012 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 8 lung 114809 RMVar_ID_114809 Human_SNP_ID_861328655 m1A Human chr5 - 78113909 78113909 78113909 TCTGGTTCTGTTTTTCAGAGAGTGAATCTGGAAGTGAAAGTGGAGAACAAGGCGAAAGTGGGGAG TCTGGTTCTGTTTTTCAGAGAGTGAATCTGGACGTGAAAGTGGAGAACAAGGCGAAAGTGGGGAG T G AP3B1 Ensembl:ENSG00000132842 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:78113751..78116225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_2946493,Human_RBP_ID_3967989,Human_RBP_ID_18413683,Human_RBP_ID_19014929,Human_RBP_ID_24117066,Human_RBP_ID_24547967,Human_RBP_ID_26350998 Human_Splice_Rec_666208,Human_Splice_Rec_666260,Human_Splice_Rec_666302 RMVar_hsa_circ_6209,RMVar_hsa_circ_101916,RMVar_hsa_circ_113230,RMVar_hsa_circ_115151,RMVar_hsa_circ_105659,RMVar_hsa_circ_232638,RMVar_hsa_circ_85016,RMVar_hsa_circ_232640,RMVar_hsa_circ_232641,RMVar_hsa_circ_232639,RMVar_hsa_circ_232637,RMVar_hsa_circ_50562,RMVar_hsa_circ_310459,RMVar_hsa_circ_332194,RMVar_hsa_circ_357103,RMVar_hsa_circ_366536,RMVar_hsa_circ_370007,RMVar_hsa_circ_355667,RMVar_hsa_circ_311049,RMVar_hsa_circ_295881,RMVar_hsa_circ_307409,RMVar_hsa_circ_290833,RMVar_hsa_circ_76410,RMVar_hsa_circ_112984,RMVar_hsa_circ_274772,RMVar_hsa_circ_102741,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_36563,RMVar_hsa_circ_232648,RMVar_hsa_circ_232652,RMVar_hsa_circ_232654,RMVar_hsa_circ_232656,RMVar_hsa_circ_232658,RMVar_hsa_circ_232657,RMVar_hsa_circ_232655,RMVar_hsa_circ_232653,RMVar_hsa_circ_232650,RMVar_hsa_circ_232651,RMVar_hsa_circ_232649,RMVar_hsa_circ_74195,RMVar_hsa_circ_232660,RMVar_hsa_circ_100287,RMVar_hsa_circ_356771,RMVar_hsa_circ_232647,RMVar_hsa_circ_360253,RMVar_hsa_circ_333887,RMVar_hsa_circ_232661,RMVar_hsa_circ_289887,RMVar_hsa_circ_358441,RMVar_hsa_circ_360737,RMVar_hsa_circ_361542,RMVar_hsa_circ_355639,RMVar_hsa_circ_232663,RMVar_hsa_circ_62264,RMVar_hsa_circ_367066,RMVar_hsa_circ_232662,RMVar_hsa_circ_358296,RMVar_hsa_circ_51630 114810 RMVar_ID_114810 Human_SNP_ID_861367259 m1A Human chr5 - 314403 314403 314403 TGAATATATCCGTCAACCTCTGGGGAGAAAACAGGCATTTAAATCTCGATAGTAAATGGAAGGAG TGAATATATCCGTCAACCTCTGGGGAGAAAACGGGCATTTAAATCTCGATAGTAAATGGAAGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:314401..314650 32194978 MeRIP-seq:(Medium) rs1574220 Functional Loss SNV ICGC 33..33 33 ESCA 2 - GWAS_ID_6660,GWAS_ID_6661,GWAS_ID_6662 114811 RMVar_ID_114811 Human_SNP_ID_861386937 m1A Human chr5 - 80854218 80854218 80854218 TCCTAGTTCATCCAAGATAACCAAGGACTGTGATGTTGCTTTTCTGATTATTTCTGCTGTGTCAG TCCTAGTTCATCCAAGATAACCAAGGACTGTGGTGTTGCTTTTCTGATTATTTCTGCTGTGTCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:80854169..80854249 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 114812 RMVar_ID_114812 Human_SNP_ID_861401356 m1A Human chr5 - 16701426 16701426 16701426 GCCCAACTTCAACTTCAGCCAGCCCTACCCAGAGGAGGAGGTCGATGAGGGCTTCGAAGCCGACG GCCCAACTTCAACTTCAGCCAGCCCTACCCAGCGGAGGAGGTCGATGAGGGCTTCGAAGCCGACG T G MYO10 Ensembl:ENSG00000145555 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:16701401..16701425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 20 liver Human_RBP_ID_75551,Human_RBP_ID_8887679,Human_RBP_ID_18043919 Human_miRNA_ID_2423625,Human_miRNA_ID_2433286 RMVar_hsa_circ_42338,RMVar_hsa_circ_92571,RMVar_hsa_circ_117899,RMVar_hsa_circ_82208,RMVar_hsa_circ_230495,RMVar_hsa_circ_230496,RMVar_hsa_circ_230498,RMVar_hsa_circ_264947,RMVar_hsa_circ_230499,RMVar_hsa_circ_126247,RMVar_hsa_circ_97329,RMVar_hsa_circ_107631,RMVar_hsa_circ_230501,RMVar_hsa_circ_110190,RMVar_hsa_circ_289935,RMVar_hsa_circ_230502,RMVar_hsa_circ_117125,RMVar_hsa_circ_95398,RMVar_hsa_circ_3584,RMVar_hsa_circ_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_74659,RMVar_hsa_circ_44006,RMVar_hsa_circ_120862,RMVar_hsa_circ_330089,RMVar_hsa_circ_230510 114813 RMVar_ID_114813 Human_SNP_ID_861409867 m1A Human chr5 - 135034156 135034150 135034156 GGCCCCGGATCGCGAGCCGGAGCCGGAGCCGGAGCCGGGGCCGGCCGGGCTGCTGAGGCCCGAGC GGCCCCGGATCGCGAGCCGGAGCCGGAGCCGG______GGCCGGCCGGGCTGCTGAGGCCCGAGC CCCGGCT C PITX1 Ensembl:ENSG00000069011 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:135034065..135034165 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..38 33 ESCA 1 - Human_RBP_ID_4845366,Human_RBP_ID_5326545,Human_RBP_ID_8894089,Human_RBP_ID_9306603 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 114814 RMVar_ID_114814 Human_SNP_ID_861412289 m1A Human chr5 + 139392675 139392675 139392675 CCCAGGGCTCGGGCTGGCTTGCATCTGAGGGGAGCCGGGGCGGGGCGATCGGACCCCTGCTGGCC CCCAGGGCTCGGGCTGGCTTGCATCTGAGGGGTGCCGGGGCGGGGCGATCGGACCCCTGCTGGCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:139392628..139392706 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 114815 RMVar_ID_114815 Human_SNP_ID_861429459 m1A Human chr5 + 179122770 179122770 179122770 CCGCTCCTGGGTGCCGTTGCCACAGGTTACTGAGCACTGCAGGGGGAGAGTCGCCAGGCAGGGTT CCGCTCCTGGGTGCCGTTGCCACAGGTTACTGGGCACTGCAGGGGGAGAGTCGCCAGGCAGGGTT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:179122721..179126071 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 114816 RMVar_ID_114816 Human_SNP_ID_861440303 m1A Human chr5 - 176238519 176238519 176238519 TCTCAGAGCCGCTGTCGTCCGAGATCACGATGAAATCCTCCATGGCTGCGGGCCCCGACCGAAGA TCTCAGAGCCGCTGTCGTCCGAGATCACGATGTAATCCTCCATGGCTGCGGGCCCCGACCGAAGA T A RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:176238487..176238600;chr5:176238480..176238584 26863196 MeRIP-seq:(Medium) rs866802577 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 THCA,lung adenocarcinoma,liver neoplasm,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma,THYM,liver hepatocellular_carcinoma 41 lung,liver,large intestine,haematopoietic and lymphoid tissue 114817 RMVar_ID_114817 Human_SNP_ID_861467501 m1A Human chr5 + 181242131 181242131 181242131 ACCAGCCAATTGCATCCACCTCACTTCTGCCCAGATTCTTCCCAAGGCCCCAGAGCTAAGTGAGC ACCAGCCAATTGCATCCACCTCACTTCTGCCCTGATTCTTCCCAAGGCCCCAGAGCTAAGTGAGC A T RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:181242126..181242150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRP 1 - RMVar_hsa_circ_236812 114818 RMVar_ID_114818 Human_SNP_ID_861482248 m1A Human chr5 - 44809001 44809001 44809001 GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGACCGCGTAGCAAAGGCCTCCAACACCTGGCCGC GCATTAGCCGCGGTGTGCAATGAAAGCCTCGGCCCGCGTAGCAAAGGCCTCCAACACCTGGCCGC T G MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:44808951..44809846;chr5:44808951..44809355;chr5:44808951..44809133;chr5:44808951..44809180 26863196 MeRIP-seq:(Medium) rs963177485 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 114819 RMVar_ID_114819 Human_SNP_ID_861485182 m1A Human chr5 - 135389069 135389066 135389069 CCACCGCCATGTCGAGCCGCGGTGGGAAGAAGAAGTCCACCAAGACGTCCAGGTCTGCCAAAGCA CCACCGCCATGTCGAGCCGCGGTGGGAAGAAG___TCCACCAAGACGTCCAGGTCTGCCAAAGCA ACTT A MACROH2A1 Ensembl:ENSG00000113648 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs766733082 Functional Loss DEL TCGA 33..35 33 STAD 1 - Human_RBP_ID_1645091,Human_RBP_ID_1987251,Human_RBP_ID_3758272,Human_RBP_ID_4845976,Human_RBP_ID_5121388,Human_RBP_ID_18057296,Human_RBP_ID_26826554 Human_Splice_Rec_693738,Human_Splice_Rec_693766,Human_Splice_Rec_693782,Human_Splice_Rec_693798,Human_Splice_Rec_693816,Human_Splice_Rec_693830,Human_Splice_Rec_693838,Human_Splice_Rec_693858,Human_Splice_Rec_693868,Human_Splice_Rec_693896 RMVar_hsa_circ_313789,RMVar_hsa_circ_305465,RMVar_hsa_circ_234641 114820 RMVar_ID_114820 Human_SNP_ID_861490613 m1A Human chr5 + 151771983 151771983 151771983 TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTACTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC TGTGTGCGGACGCAGTTGCGTGAGGGGTTTGTGCTATCCTCGGTGCTGTGGTGCAGAGCTAGTTC A G G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2915874 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,ESCA 4 prostate Human_RBP_ID_75800,Human_RBP_ID_635578,Human_RBP_ID_788038,Human_RBP_ID_1039972,Human_RBP_ID_1211436,Human_RBP_ID_1648445,Human_RBP_ID_1990646,Human_RBP_ID_4818450,Human_RBP_ID_5477120,Human_RBP_ID_7406746,Human_RBP_ID_8607840,Human_RBP_ID_8886736,Human_RBP_ID_9306796,Human_RBP_ID_9335416,Human_RBP_ID_17707393,Human_RBP_ID_18057401,Human_RBP_ID_18425036,Human_RBP_ID_18448380,Human_RBP_ID_18836607,Human_RBP_ID_21900800,Human_RBP_ID_26530702,Human_RBP_ID_27076633,Human_RBP_ID_27333259 Human_Splice_Rec_712509,Human_Splice_Rec_712531,Human_Splice_Rec_712553,Human_Splice_Rec_712555,Human_Splice_Rec_712561,Human_Splice_Rec_712571,Human_Splice_Rec_712579,Human_Splice_Rec_712587,Human_Splice_Rec_712607 Human_miRNA_ID_1955339,Human_miRNA_ID_2055165,Human_miRNA_ID_2501914 GWAS_ID_10044,GWAS_ID_10045,GWAS_ID_10046,GWAS_ID_10047,GWAS_ID_10048,GWAS_ID_10049,GWAS_ID_10050,GWAS_ID_10051,GWAS_ID_10052,GWAS_ID_10053,GWAS_ID_10054,GWAS_ID_10055,GWAS_ID_10056,GWAS_ID_10057,GWAS_ID_10058,GWAS_ID_10059,GWAS_ID_10060,GWAS_ID_10061,GWAS_ID_10062,GWAS_ID_10063,GWAS_ID_10064,GWAS_ID_10065,GWAS_ID_10066,GWAS_ID_10067,GWAS_ID_10068,GWAS_ID_10069 RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619 114821 RMVar_ID_114821 Human_SNP_ID_861492094 m1A Human chr5 + 126826052 126826052 126826052 CCCCCCAACTGACCTCATCTGGAAGAACCAGAACTCGTGGGGCACTGGCGAAGATGTGAAGGTTA CCCCCCAACTGACCTCATCTGGAAGAACCAGACCTCGTGGGGCACTGGCGAAGATGTGAAGGTTA A C LMNB1 Ensembl:ENSG00000113368 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:126826001..126826125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_1643695,Human_RBP_ID_1985521,Human_RBP_ID_3755721,Human_RBP_ID_4806380,Human_RBP_ID_5508756,Human_RBP_ID_7375815,Human_RBP_ID_8600904,Human_RBP_ID_8883585,Human_RBP_ID_15281351,Human_RBP_ID_18037183,Human_RBP_ID_18448000,Human_RBP_ID_18537683,Human_RBP_ID_18831177,Human_RBP_ID_22771431,Human_RBP_ID_24080110 Human_Splice_Rec_686670,Human_Splice_Rec_686671,Human_Splice_Rec_686690,Human_Splice_Rec_686691,Human_Splice_Rec_686710,Human_Splice_Rec_686711 Human_miRNA_ID_218770 RMVar_hsa_circ_111166,RMVar_hsa_circ_234092,RMVar_hsa_circ_278490,RMVar_hsa_circ_269995,RMVar_hsa_circ_234099,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_336793,RMVar_hsa_circ_301602 114822 RMVar_ID_114822 Human_SNP_ID_861496653 m1A Human chr5 + 150449480 150449480 150449480 GCGGGGCCGAGGCCTTAAAAGGCTGGACCCGCACTCACCCTTACTTCACAAGCTCCTCCCTGAAA GCGGGGCCGAGGCCTTAAAAGGCTGGACCCGCGCTCACCCTTACTTCACAAGCTCCTCCCTGAAA A G lnc-NDST1-1,lnc-NDST1-1:2,lnc-NDST1-1:3,lnc-NDST1-1:4 RNACentral:URS0000D5DC92,RNACentral:URS0000D59089,RNACentral:URS00008BB333,RNACentral:URS00008B4F63 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:150449476..150449675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 114823 RMVar_ID_114823 Human_SNP_ID_861508131 m1A Human chr5 - 122027350 122027350 122027350 AAGAGACTTATTCAAATACGAGTTTAAGTAATAGCTGCAGAGCCTGGGGTGAGAAAGCTGGGCAT AAGAGACTTATTCAAATACGAGTTTAAGTAATGGCTGCAGAGCCTGGGGTGAGAAAGCTGGGCAT T C HSALNG0044458 RNACentral:URS0000E92C78 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:122027308..122027386 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 114824 RMVar_ID_114824 Human_SNP_ID_861508632 m1A Human chr5 + 1540085 1540085 1540085 ACAGGGCCACACAGAGCCACACGGGGCCACACAGGGTCACACAGAGCCACACGGGGTCACACAGA ACAGGGCCACACAGAGCCACACGGGGCCACACGGGGTCACACAGAGCCACACGGGGTCACACAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:1540036..1540160 26863196 MeRIP-seq:(Medium) rs1279852147 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114825 RMVar_ID_114825 Human_SNP_ID_861547678 m1A Human chr5 + 140664917 140664917 140664917 GGCGGCGCGGCTCGCAGTCCTTCTCAGCATGGACCGCACTTGTGAGGAGAGGCCCGCTGAGGATG GGCGGCGCGGCTCGCAGTCCTTCTCAGCATGGCCCGCACTTGTGAGGAGAGGCCCGCTGAGGATG A C WDR55 Ensembl:ENSG00000120314 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140664870..140665019 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 1 ovary Human_RBP_ID_4846042,Human_RBP_ID_22827407,Human_RBP_ID_23050287 114826 RMVar_ID_114826 Human_SNP_ID_861552327 m1A Human chr5 + 134158496 134158496 134158496 CTCCTCTTCAGTAAAGTCATTTTTGATATTGAAGGTCTTGCGAATCTCCTCAGGAGTTTTCCCCT CTCCTCTTCAGTAAAGTCATTTTTGATATTGACGGTCTTGCGAATCTCCTCAGGAGTTTTCCCCT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:134158452..134158531 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 5 haematopoietic and lymphoid tissue 114827 RMVar_ID_114827 Human_SNP_ID_861562332 m1A Human chr5 + 140114308 140114308 140114308 GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCAGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG GGGGCGGTGGTGGCGGCGGGGGCGGCGGCGGCGGTGGCGGCGGCGGCGGCGGGGCCCCAGGGGGG A G PURA Ensembl:ENSG00000185129 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr5:140114126..140114373 26863410 MeRIP-seq:(Medium) rs1335796595 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 1 haematopoietic and lymphoid tissue Human_RBP_ID_214396,Human_RBP_ID_250980,Human_RBP_ID_3783399,Human_RBP_ID_5242441,Human_RBP_ID_8730244,Human_RBP_ID_9335377,Human_RBP_ID_22099710,Human_RBP_ID_22727492,Human_RBP_ID_23258903,Human_RBP_ID_26792162,Human_RBP_ID_27075005 114828 RMVar_ID_114828 Human_SNP_ID_861568442 m1A Human chr5 + 177456041 177456041 177456041 GGGTCTTCCCCAGCTGGACCGACTCAGAGCTCAGCAGCCGCGAGCCCCTGGAGCACGGAGCTTGG GGGTCTTCCCCAGCTGGACCGACTCAGAGCTCCGCAGCCGCGAGCCCCTGGAGCACGGAGCTTGG A C PRR7 Ensembl:ENSG00000131188 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:177455941..177456040 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_167008,Human_RBP_ID_5121492,Human_RBP_ID_24099190 114829 RMVar_ID_114829 Human_SNP_ID_861571279 m1A Human chr5 + 17354331 17354331 17354331 AAAGTAGTAAGACATGGACAGGTAAACGCAGGAGGCGTAGAGCTCCAGGTTGATCTGGCGGTTGA AAAGTAGTAAGACATGGACAGGTAAACGCAGGTGGCGTAGAGCTCCAGGTTGATCTGGCGGTTGA A T AC026785.2 Ensembl:ENSG00000248223 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:17354316..17354399 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_5616857 114830 RMVar_ID_114830 Human_SNP_ID_861573142 m1A Human chr5 + 139369039 139369039 139369039 TGGCTTGATGTGAAGACAGCAAGGAAAGAAGCACCAGTCAAGTTGTGAACAAGCACCAAATTAAA TGGCTTGATGTGAAGACAGCAAGGAAAGAAGCGCCAGTCAAGTTGTGAACAAGCACCAAATTAAA A G PAIP2 Ensembl:ENSG00000120727 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139364676..139369149 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,kidney papillary_renal_cell_carcinoma,KIRP 12 kidney Human_RBP_ID_633098,Human_RBP_ID_1646108,Human_RBP_ID_1988329,Human_RBP_ID_7392729,Human_RBP_ID_9170502,Human_RBP_ID_17527669,Human_RBP_ID_18353981,Human_RBP_ID_22458962,Human_RBP_ID_26529283 114831 RMVar_ID_114831 Human_SNP_ID_861579852 m1A Human chr5 - 141524229 141524229 141524229 AGTTCACATCTCCATCTTGTTCTTTATAACAGAGGGCGATGAGACAGGTGTGATGGACAGTCTTC AGTTCACATCTCCATCTTGTTCTTTATAACAGCGGGCGATGAGACAGGTGTGATGGACAGTCTTC T G DIAPH1 Ensembl:ENSG00000131504 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:141524097..141524284;chr5:141524151..141524291;chr5:141518995..141524291;chr5:141518995..141524295 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_22459780 Human_Splice_Rec_701677,Human_Splice_Rec_701724,Human_Splice_Rec_701725,Human_Splice_Rec_701772,Human_Splice_Rec_701773,Human_Splice_Rec_701818,Human_Splice_Rec_701819,Human_Splice_Rec_701860,Human_Splice_Rec_701861,Human_Splice_Rec_701904,Human_Splice_Rec_701905,Human_Splice_Rec_701908,Human_Splice_Rec_701909,Human_Splice_Rec_701911,Human_Splice_Rec_701958,Human_Splice_Rec_701959,Human_Splice_Rec_701961,Human_Splice_Rec_701963 RMVar_hsa_circ_97418,RMVar_hsa_circ_122810,RMVar_hsa_circ_124098,RMVar_hsa_circ_119624,RMVar_hsa_circ_38438,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_87304,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_235084,RMVar_hsa_circ_76306,RMVar_hsa_circ_76374,RMVar_hsa_circ_235086,RMVar_hsa_circ_235087,RMVar_hsa_circ_235085,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_56396,RMVar_hsa_circ_235088 114832 RMVar_ID_114832 Human_SNP_ID_861579854 m1A Human chr5 - 141524229 141524229 141524229 AGTTCACATCTCCATCTTGTTCTTTATAACAGAGGGCGATGAGACAGGTGTGATGGACAGTCTTC AGTTCACATCTCCATCTTGTTCTTTATAACAGTGGGCGATGAGACAGGTGTGATGGACAGTCTTC T A DIAPH1 Ensembl:ENSG00000131504 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr5:141524097..141524284;chr5:141524151..141524291;chr5:141518995..141524291;chr5:141518995..141524295 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_22459780 Human_Splice_Rec_701677,Human_Splice_Rec_701724,Human_Splice_Rec_701725,Human_Splice_Rec_701772,Human_Splice_Rec_701773,Human_Splice_Rec_701818,Human_Splice_Rec_701819,Human_Splice_Rec_701860,Human_Splice_Rec_701861,Human_Splice_Rec_701904,Human_Splice_Rec_701905,Human_Splice_Rec_701908,Human_Splice_Rec_701909,Human_Splice_Rec_701911,Human_Splice_Rec_701958,Human_Splice_Rec_701959,Human_Splice_Rec_701961,Human_Splice_Rec_701963 RMVar_hsa_circ_97418,RMVar_hsa_circ_122810,RMVar_hsa_circ_124098,RMVar_hsa_circ_119624,RMVar_hsa_circ_38438,RMVar_hsa_circ_76385,RMVar_hsa_circ_85369,RMVar_hsa_circ_87304,RMVar_hsa_circ_84414,RMVar_hsa_circ_235080,RMVar_hsa_circ_235084,RMVar_hsa_circ_76306,RMVar_hsa_circ_76374,RMVar_hsa_circ_235086,RMVar_hsa_circ_235087,RMVar_hsa_circ_235085,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_56396,RMVar_hsa_circ_235088 114833 RMVar_ID_114833 Human_SNP_ID_861600561 m1A Human chr5 - 93593709 93593709 93593709 CGAAGAAGAGCTGCTCGATGACGGAGGAGGACACGGTGCGCAGCGAGGGCAGTCGCAGCAGCAGT CGAAGAAGAGCTGCTCGATGACGGAGGAGGACCCGGTGCGCAGCGAGGGCAGTCGCAGCAGCAGT T G NR2F1-AS1 RNACentral:URS00008C00C8 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:93593659..93593769 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 6 ovary 114834 RMVar_ID_114834 Human_SNP_ID_861623544 m1A Human chr5 + 306753 306753 306753 ATCGATAAGAACGAGCTGAAGCAGGCCCTCTCAGGTTTCGGTAACTCACTCACTCTGGCTTGTGT ATCGATAAGAACGAGCTGAAGCAGGCCCTCTCGGGTTTCGGTAACTCACTCACTCTGGCTTGTGT A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,3'UTR,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:306601..306775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus Human_RBP_ID_640904,Human_RBP_ID_9398839,Human_RBP_ID_15420036,Human_RBP_ID_19124228 Human_Splice_Rec_631001,Human_Splice_Rec_631021,Human_Splice_Rec_631029,Human_Splice_Rec_631039,Human_Splice_Rec_631049,Human_Splice_Rec_631069,Human_Splice_Rec_631077,Human_Splice_Rec_631085 RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229944,RMVar_hsa_circ_80928,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_294234 114835 RMVar_ID_114835 Human_SNP_ID_861630153 m1A Human chr5 - 138466963 138466963 138466963 GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGACGAGGAGGCCGGTGGGTTGGTCATGCTCACTA GGCGGAGGAGGCCGCTGGAGATGGTGCTGAGGCCGAGGAGGCCGGTGGGTTGGTCATGCTCACTA T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:138466773..138467193 26863196 MeRIP-seq:(Medium) rs201570244 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue 114836 RMVar_ID_114836 Human_SNP_ID_861647444 m1A Human chr5 + 151786621 151786621 151786621 TCTTTTCCCCCCAGGTTGAATTGACCAAAGCAATGGTGATGGAGAAGCCTAGTCCCCTGCTGGTC TCTTTTCCCCCCAGGTTGAATTGACCAAAGCAGTGGTGATGGAGAAGCCTAGTCCCCTGCTGGTC A G G3BP1 Ensembl:ENSG00000145907 Protein coding start codon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:151786541..151786702 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_RBP_ID_946764,Human_RBP_ID_1211447,Human_RBP_ID_1648455,Human_RBP_ID_1990676,Human_RBP_ID_3763057,Human_RBP_ID_3967566,Human_RBP_ID_4818470,Human_RBP_ID_5151693,Human_RBP_ID_5509111,Human_RBP_ID_7406924,Human_RBP_ID_9335791,Human_RBP_ID_15355164,Human_RBP_ID_18042594,Human_RBP_ID_18836622,Human_RBP_ID_22459006,Human_RBP_ID_22680908,Human_RBP_ID_25933396 Human_Splice_Rec_712498,Human_Splice_Rec_712499,Human_Splice_Rec_712504,Human_Splice_Rec_712505,Human_Splice_Rec_712510,Human_Splice_Rec_712511,Human_Splice_Rec_712532,Human_Splice_Rec_712533,Human_Splice_Rec_712554,Human_Splice_Rec_712556,Human_Splice_Rec_712557,Human_Splice_Rec_712562,Human_Splice_Rec_712563,Human_Splice_Rec_712572,Human_Splice_Rec_712573,Human_Splice_Rec_712580,Human_Splice_Rec_712581,Human_Splice_Rec_712588,Human_Splice_Rec_712589,Human_Splice_Rec_712608,Human_Splice_Rec_712609,Human_Splice_Rec_712630,Human_Splice_Rec_712631,Human_Splice_Rec_712636,Human_Splice_Rec_712637,Human_Splice_Rec_712645 RMVar_hsa_circ_10319,RMVar_hsa_circ_84068,RMVar_hsa_circ_235618,RMVar_hsa_circ_81022,RMVar_hsa_circ_124631,RMVar_hsa_circ_235619,RMVar_hsa_circ_275819,RMVar_hsa_circ_293465,RMVar_hsa_circ_331186,RMVar_hsa_circ_349760,RMVar_hsa_circ_298406,RMVar_hsa_circ_276184,RMVar_hsa_circ_115515,RMVar_hsa_circ_271413,RMVar_hsa_circ_101706,RMVar_hsa_circ_235623,RMVar_hsa_circ_235627,RMVar_hsa_circ_34371,RMVar_hsa_circ_77316,RMVar_hsa_circ_235629,RMVar_hsa_circ_235630,RMVar_hsa_circ_235628,RMVar_hsa_circ_235625,RMVar_hsa_circ_235626,RMVar_hsa_circ_235624,RMVar_hsa_circ_235621,RMVar_hsa_circ_235622,RMVar_hsa_circ_309286,RMVar_hsa_circ_321849,RMVar_hsa_circ_322634,RMVar_hsa_circ_310132,RMVar_hsa_circ_73757,RMVar_hsa_circ_235631 114837 RMVar_ID_114837 Human_SNP_ID_861651035 m1A Human chr5 - 177467629 177467629 177467629 GTGCCGCCTGAGCACTGCCGTCTTCTTGCGGAAGGGTGTCGACGTGATCGTGAACGCCAGCAGCG GTGCCGCCTGAGCACTGCCGTCTTCTTGCGGAGGGGTGTCGACGTGATCGTGAACGCCAGCAGCG T C DBN1 Ensembl:ENSG00000113758 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:177467442..177467652 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_943200,Human_RBP_ID_3968449,Human_RBP_ID_5395870,Human_RBP_ID_19126857,Human_RBP_ID_23258925,Human_RBP_ID_26351817,Human_RBP_ID_26792261,Human_RBP_ID_27079146 RMVar_hsa_circ_121989,RMVar_hsa_circ_41429,RMVar_hsa_circ_236500,RMVar_hsa_circ_53146,RMVar_hsa_circ_117081,RMVar_hsa_circ_236503,RMVar_hsa_circ_45910,RMVar_hsa_circ_48493,RMVar_hsa_circ_26260,RMVar_hsa_circ_34573,RMVar_hsa_circ_93340,RMVar_hsa_circ_236504 114838 RMVar_ID_114838 Human_SNP_ID_861654246 m1A Human chr5 - 126787926 126787926 126787926 CCAGAATGATCATGTCACAATTCTGCCTTAAAATCTTGGGTCCACTCATTACTAAAAATACAATC CCAGAATGATCATGTCACAATTCTGCCTTAAAGTCTTGGGTCCACTCATTACTAAAAATACAATC T C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:126787924..126788135 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114839 RMVar_ID_114839 Human_SNP_ID_861689998 m1A Human chr5 - 154800025 154800025 154800025 CAAGGCCTCACCCACCTTGGGCCGTGCTGGGGATGGCCGAGGCCTCTTCTTCACTTCAATCCAGT CAAGGCCTCACCCACCTTGGGCCGTGCTGGGGGTGGCCGAGGCCTCTTCTTCACTTCAATCCAGT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:154799976..154800050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 DLBC 2 - 114840 RMVar_ID_114840 Human_SNP_ID_861749351 m1A Human chr5 - 176649152 176649152 176649152 CATTCCAAACCTCCAGGCCCTGCCCCTCATCCACCCTCCACACAGCAGCCAGGCAAGCGGTCTCC CATTCCAAACCTCCAGGCCCTGCCCCTCATCCCCCCTCCACACAGCAGCCAGGCAAGCGGTCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:176649150..176649317 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 114841 RMVar_ID_114841 Human_SNP_ID_861752049 m1A Human chr5 + 69189729 69189729 69189729 GGCAGGCGGGCCACCGCAGGTCGCCGGCGCCCAGGCGGCGTGCAGCGAGGACCGCATGACCCTGC GGCAGGCGGGCCACCGCAGGTCGCCGGCGCCCGGGCGGCGTGCAGCGAGGACCGCATGACCCTGC A G CENPH Ensembl:ENSG00000153044 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:69189626..69189775 32194978 MeRIP-seq:(Medium) rs1388942127 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_250230,Human_RBP_ID_4845753,Human_RBP_ID_9335237,Human_RBP_ID_22460074 Human_Splice_Rec_658065,Human_Splice_Rec_658079,Human_Splice_Rec_658095,Human_Splice_Rec_658105,Human_Splice_Rec_658113 RMVar_hsa_circ_103108,RMVar_hsa_circ_232023 114842 RMVar_ID_114842 Human_SNP_ID_861766086 m1A Human chr5 + 172284014 172284014 172284014 CCCTCACAGCCCCGCACACCCGAGTCCAGGCGAGCCCCGCGCCGGCGCCTCGCGTCCGCCAGGAC CCCTCACAGCCCCGCACACCCGAGTCCAGGCGGGCCCCGCGCCGGCGCCTCGCGTCCGCCAGGAC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,ALKBH3 KO;HEK293T,untreat control chr5:172283913..172284058;chr5:172283630..172284089 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114843 RMVar_ID_114843 Human_SNP_ID_861780314 m1A Human chr5 - 132997818 132997818 132997818 AAAGAAAGCAGCCATGTAAGAGGCTAACTTAAATAGAAGTGCTAGAAATATCTTTGTGTATTAAC AAAGAAAGCAGCCATGTAAGAGGCTAACTTAAGTAGAAGTGCTAGAAATATCTTTGTGTATTAAC T C ZCCHC10 Ensembl:ENSG00000155329 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3210524 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_miRNA_ID_2363741 RMVar_hsa_circ_78262,RMVar_hsa_circ_234412 114844 RMVar_ID_114844 Human_SNP_ID_861791266 m1A Human chr5 - 177311486 177311486 177311486 CCAGCCTGACGCGGGCGGGGACTCTCTCTGGCAGAGGCCGAGCATGGTTATGCGTCCCTGTGCCC CCAGCCTGACGCGGGCGGGGACTCTCTCTGGCGGAGGCCGAGCATGGTTATGCGTCCCTGTGCCC T C MXD3 Ensembl:ENSG00000213347 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:177311445..177311841 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 4 breast Human_RBP_ID_251002,Human_RBP_ID_19125028,Human_RBP_ID_22553413,Human_RBP_ID_22681284,Human_RBP_ID_25934350 Human_Splice_Rec_724666 114845 RMVar_ID_114845 Human_SNP_ID_861794015 m1A Human chr5 + 151259848 151259848 151259848 TCAGAAGCCTGACTCTGGAGCCTGACCCCATCATCGTTCCTGGAAATGTGACCCTCAGTGTCATG TCAGAAGCCTGACTCTGGAGCCTGACCCCATCGTCGTTCCTGGAAATGTGACCCTCAGTGTCATG A G GM2A Ensembl:ENSG00000196743 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs153477 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,COCA,central_nervous_system oligodendroglioma_Grade_II,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue,brain Human_RBP_ID_5509103,Human_RBP_ID_22459345,Human_RBP_ID_22771488,Human_RBP_ID_24091380 Human_Splice_Rec_712014,Human_Splice_Rec_712015,Human_Splice_Rec_712018,Human_Splice_Rec_712019,Human_Splice_Rec_712023 Clinvar_Rec_429 GWAS_ID_10017,GWAS_ID_10018,GWAS_ID_10019,GWAS_ID_10020,GWAS_ID_10021,GWAS_ID_10022,GWAS_ID_10023,GWAS_ID_10024,GWAS_ID_10025,GWAS_ID_10026,GWAS_ID_10027,GWAS_ID_10028,GWAS_ID_10029,GWAS_ID_10030,GWAS_ID_10031,GWAS_ID_10032,GWAS_ID_10033,GWAS_ID_10034,GWAS_ID_10035,GWAS_ID_10036,GWAS_ID_10037 114846 RMVar_ID_114846 Human_SNP_ID_861796211 m1A Human chr5 + 146128763 146128763 146128763 CCACATAGATGGTGCAATGTGAGGGCTTCTGCAGGGGTTGTTTGTCAGTCTTCTAGACGGTAAAA CCACATAGATGGTGCAATGTGAGGGCTTCTGCGGGGGTTGTTTGTCAGTCTTCTAGACGGTAAAA A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:146128714..146128821 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 114847 RMVar_ID_114847 Human_SNP_ID_861816579 m1A Human chr5 - 171387900 171387899 171387900 CTTAGGTAGGAGAGAAGGCGGACGGAGATAAAAGAACGCTGCTCCAGAGAACAACCGCGCAGGAC CTTAGGTAGGAGAGAAGGCGGACGGAGATAAA_GAACGCTGCTCCAGAGAACAACCGCGCAGGAC CT C RF00017-4506 RNACentral:URS000096AE3B SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:171387851..171387950 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 114848 RMVar_ID_114848 Human_SNP_ID_861822359 m1A Human chr5 + 143400845 143400844 143400846 AGGAGTTAATGATTCTTTGGAGTCCATCAGTGAATATCAACTACAAAACAAAAAACAAAAACGGG AGGAGTTAATGATTCTTTGGAGTCCATCAGTG__TATCAACTACAAAACAAAAAACAAAAACGGG GAA G KU921432 RNACentral:URS0000A3C9C3 Other intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:143400797..143400882 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 GBM 1 - 114849 RMVar_ID_114849 Human_SNP_ID_861823381 m1A Human chr5 + 139322027 139322027 139322027 ACCTGTCTGAGAAATATAAAAAACTGGTTCTGAGGGTATGTAGTATTTGATTTGTCATCATTTAA ACCTGTCTGAGAAATATAAAAAACTGGTTCTGTGGGTATGTAGTATTTGATTTGTCATCATTTAA A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:139319364..139322465 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 12 liver Human_RBP_ID_214080,Human_RBP_ID_944583,Human_RBP_ID_1039279,Human_RBP_ID_1988222,Human_RBP_ID_5532038,Human_RBP_ID_8885077,Human_RBP_ID_9398307,Human_RBP_ID_15320225,Human_RBP_ID_19126362,Human_RBP_ID_24385491,Human_RBP_ID_26351383,Human_RBP_ID_27826832 Human_Splice_Rec_697495,Human_Splice_Rec_697547,Human_Splice_Rec_697583,Human_Splice_Rec_697617,Human_Splice_Rec_697651,Human_Splice_Rec_697827,Human_Splice_Rec_697855,Human_Splice_Rec_697887,Human_Splice_Rec_697933,Human_Splice_Rec_697961,Human_Splice_Rec_697995,Human_Splice_Rec_698039,Human_Splice_Rec_698063,Human_Splice_Rec_698073 RMVar_hsa_circ_234897,RMVar_hsa_circ_91210,RMVar_hsa_circ_116622,RMVar_hsa_circ_234892,RMVar_hsa_circ_101392,RMVar_hsa_circ_85144,RMVar_hsa_circ_234898,RMVar_hsa_circ_56035,RMVar_hsa_circ_234896,RMVar_hsa_circ_114464,RMVar_hsa_circ_62131,RMVar_hsa_circ_234916,RMVar_hsa_circ_80966,RMVar_hsa_circ_55566,RMVar_hsa_circ_234918,RMVar_hsa_circ_43369,RMVar_hsa_circ_234919,RMVar_hsa_circ_72323,RMVar_hsa_circ_288584,RMVar_hsa_circ_59656,RMVar_hsa_circ_61079,RMVar_hsa_circ_70005,RMVar_hsa_circ_234921,RMVar_hsa_circ_345023,RMVar_hsa_circ_70332,RMVar_hsa_circ_62675,RMVar_hsa_circ_62835,RMVar_hsa_circ_33277,RMVar_hsa_circ_320086 114850 RMVar_ID_114850 Human_SNP_ID_861845094 m1A Human chr5 - 138286135 138286135 138286135 TTCCACCCCACCCATCTCTGGGTTCTCTCTAAAGGTGCCGCTGTCTGCGTGAAGAGGACAGGTCT TTCCACCCCACCCATCTCTGGGTTCTCTCTAACGGTGCCGCTGTCTGCGTGAAGAGGACAGGTCT T G CDC25C Ensembl:ENSG00000158402 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:138286093..138289507 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin acral_lentiginous 5 skin 114851 RMVar_ID_114851 Human_SNP_ID_861851507 m1A Human chr5 + 181204778 181204778 181204778 GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCAGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT GCGGCCGCCTGAGACCCGTGCTCTCCCGGGGCGGCCGCGGGCAGGCTGAAGCGCCGCAGGAGCGT A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr5:181204727..181204831 26863196 MeRIP-seq:(Medium) rs2770944 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114852 RMVar_ID_114852 Human_SNP_ID_861862039 m1A Human chr5 + 168464945 168464945 168464945 TGCGTGAGGACGAGCGTTTCCGCCTGCTGCTGAGGATGCTGGAGAAGCGGGTGAGTTCTGCCTCG TGCGTGAGGACGAGCGTTTCCGCCTGCTGCTGTGGATGCTGGAGAAGCGGGTGAGTTCTGCCTCG A T WWC1 Ensembl:ENSG00000113645 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:168464895..168467726 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_718367,Human_Splice_Rec_718411,Human_Splice_Rec_718469,Human_Splice_Rec_718519,Human_Splice_Rec_718553,Human_Splice_Rec_718569,Human_Splice_Rec_718571 RMVar_hsa_circ_268954,RMVar_hsa_circ_52776,RMVar_hsa_circ_17733,RMVar_hsa_circ_11114 114853 RMVar_ID_114853 Human_SNP_ID_861893057 m1A Human chr5 - 41805623 41805623 41805623 TGGGGAAGCCAAATCTGCTAAACCTGGAGATGACGTAAGGGAACGAATCATCAAGAGGGCCGCTC TGGGGAAGCCAAATCTGCTAAACCTGGAGATGGCGTAAGGGAACGAATCATCAAGAGGGCCGCTC T C OXCT1 Ensembl:ENSG00000083720 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:41805566..41807416 32194978 MeRIP-seq:(Medium) rs534151467 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_3967193 Human_Splice_Rec_647196,Human_Splice_Rec_647197,Human_Splice_Rec_647238,Human_Splice_Rec_647239 RMVar_hsa_circ_73658,RMVar_hsa_circ_340632,RMVar_hsa_circ_231201,RMVar_hsa_circ_272265,RMVar_hsa_circ_275995,RMVar_hsa_circ_77946,RMVar_hsa_circ_3789,RMVar_hsa_circ_11519,RMVar_hsa_circ_231203,RMVar_hsa_circ_231202,RMVar_hsa_circ_281189,RMVar_hsa_circ_45857,RMVar_hsa_circ_34953,RMVar_hsa_circ_231207,RMVar_hsa_circ_284570,RMVar_hsa_circ_107058,RMVar_hsa_circ_231209,RMVar_hsa_circ_231210,RMVar_hsa_circ_110894,RMVar_hsa_circ_231212 114854 RMVar_ID_114854 Human_SNP_ID_861893416 m1A Human chr5 - 140647885 140647885 140647885 CTCCGGCATTTTGTTATCGTTCTTTCGCTGTCACCAACAATCGAGTCTCCAACAGCAACACCGCA CTCCGGCATTTTGTTATCGTTCTTTCGCTGTCGCCAACAATCGAGTCTCCAACAGCAACACCGCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr5:140647817..140647970 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 114855 RMVar_ID_114855 Human_SNP_ID_861950156 m1A Human chr5 + 648483 648483 648483 TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTATGACTGTGAGGTGTGACTGTGAGGTGTGGACT TGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGACTGTGAGGTGTGGACT A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr5:648441..648545;chr5:648426..648558 26863196 MeRIP-seq:(Medium) rs62639482 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_5655494,Human_RBP_ID_24124148 RMVar_hsa_circ_108129,RMVar_hsa_circ_229964,RMVar_hsa_circ_127958,RMVar_hsa_circ_229971 114856 RMVar_ID_114856 Human_SNP_ID_861974056 m1A Human chr5 - 40835194 40835194 40835194 CCTTCTCTTCCGGTCTTTCTGGTCTCGGCCGCAGAAGCGAGATGGTGAGTTGTGACTGTGGTGTT CCTTCTCTTCCGGTCTTTCTGGTCTCGGCCGCTGAAGCGAGATGGTGAGTTGTGACTGTGGTGTT T A RPL37 Ensembl:ENSG00000145592 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:40835176..40835225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KICH 1 - Human_RBP_ID_250151,Human_RBP_ID_787974,Human_RBP_ID_839179,Human_RBP_ID_943345,Human_RBP_ID_1041518,Human_RBP_ID_1321669,Human_RBP_ID_4845679,Human_RBP_ID_7440146,Human_RBP_ID_9335210,Human_RBP_ID_17662305,Human_RBP_ID_18424946,Human_RBP_ID_19124413,Human_RBP_ID_22460018,Human_RBP_ID_26792060,Human_RBP_ID_26826244 Human_Splice_Rec_646675,Human_Splice_Rec_646685,Human_Splice_Rec_646701 RMVar_hsa_circ_86471,RMVar_hsa_circ_231194 114857 RMVar_ID_114857 Human_SNP_ID_861977457 m1A Human chr5 + 140673387 140673387 140673387 CCTTGTTCTCTGGATTCACCCTCTCACACCACAGCTGAGAGGGAAAGGAAGGTTGGAATGGCGGA CCTTGTTCTCTGGATTCACCCTCTCACACCACGGCTGAGAGGGAAAGGAAGGTTGGAATGGCGGA A G WDR55 Ensembl:ENSG00000120314 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:140673372..140673472 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_18040625 114858 RMVar_ID_114858 Human_SNP_ID_862001976 m1A Human chr5 - 151673160 151673159 151673161 CAGGTGGAAGTAGGAGAATTTGATGATGGTGCAGAGGAAACCGAAGAGGAGGTGGTGGCGGAAAG CAGGTGGAAGTAGGAGAATTTGATGATGGTG__GAGGAAACCGAAGAGGAGGTGGTGGCGGAAAG CTG C SPARC Ensembl:ENSG00000113140 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:151673126..151673225 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 LICA 1 - Human_RBP_ID_946399,Human_RBP_ID_22459841,Human_RBP_ID_22772147 Human_Splice_Rec_712380,Human_Splice_Rec_712381,Human_Splice_Rec_712408,Human_Splice_Rec_712409,Human_Splice_Rec_712426,Human_Splice_Rec_712427,Human_Splice_Rec_712434,Human_Splice_Rec_712442 RMVar_hsa_circ_102158,RMVar_hsa_circ_235592,RMVar_hsa_circ_107924,RMVar_hsa_circ_120704,RMVar_hsa_circ_235598,RMVar_hsa_circ_118762,RMVar_hsa_circ_102976,RMVar_hsa_circ_85030,RMVar_hsa_circ_235604,RMVar_hsa_circ_235605,RMVar_hsa_circ_235606,RMVar_hsa_circ_347507,RMVar_hsa_circ_113340,RMVar_hsa_circ_235608,RMVar_hsa_circ_118422,RMVar_hsa_circ_87743,RMVar_hsa_circ_235610,RMVar_hsa_circ_235611,RMVar_hsa_circ_235609 114859 RMVar_ID_114859 Human_SNP_ID_862019714 m1A Human chr5 + 171390102 171390102 171390102 CAAAGATTATCACTTTAAGGTGGATAATGATGAAAATGAGCACCAGTTATCTTTAAGAACGGTAC CAAAGATTATCACTTTAAGGTGGATAATGATGGAAATGAGCACCAGTTATCTTTAAGAACGGTAC A G NPM1 Ensembl:ENSG00000181163 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:171390051..171390150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_9174371,Human_RBP_ID_9398651,Human_RBP_ID_18057451,Human_RBP_ID_24095945,Human_RBP_ID_26352876 Human_Splice_Rec_720626,Human_Splice_Rec_720627,Human_Splice_Rec_720646,Human_Splice_Rec_720647,Human_Splice_Rec_720676,Human_Splice_Rec_720677,Human_Splice_Rec_720694,Human_Splice_Rec_720695,Human_Splice_Rec_720712,Human_Splice_Rec_720714,Human_Splice_Rec_720715,Human_Splice_Rec_720718,Human_Splice_Rec_720719,Human_Splice_Rec_720725 Human_miRNA_ID_2920364,Human_miRNA_ID_2920365 RMVar_hsa_circ_236196,RMVar_hsa_circ_78173,RMVar_hsa_circ_95416,RMVar_hsa_circ_80317,RMVar_hsa_circ_236198,RMVar_hsa_circ_76390,RMVar_hsa_circ_236199,RMVar_hsa_circ_236197,RMVar_hsa_circ_236200,RMVar_hsa_circ_93388,RMVar_hsa_circ_322725,RMVar_hsa_circ_362239,RMVar_hsa_circ_372404,RMVar_hsa_circ_359364,RMVar_hsa_circ_95388,RMVar_hsa_circ_236202,RMVar_hsa_circ_236203,RMVar_hsa_circ_236201 114860 RMVar_ID_114860 Human_SNP_ID_862028406 m1A Human chr5 - 1057602 1057602 1057602 GACAGGAACACCGCGTCCCACACCGCGGCGGCAGCCAGGACCCAAGCGCCGCCTACGCCAGACAA GACAGGAACACCGCGTCCCACACCGCGGCGGCGGCCAGGACCCAAGCGCCGCCTACGCCAGACAA T C SLC12A7 Ensembl:ENSG00000113504 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:1057554..1057677 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_Splice_Rec_632136,Human_Splice_Rec_632176,Human_Splice_Rec_632186,Human_Splice_Rec_632200 RMVar_hsa_circ_7593,RMVar_hsa_circ_268702,RMVar_hsa_circ_265701,RMVar_hsa_circ_89436,RMVar_hsa_circ_307998,RMVar_hsa_circ_230008 114861 RMVar_ID_114861 Human_SNP_ID_862033944 m1A Human chr5 - 64804330 64804330 64804330 ACTTCTCCTTCTCCAGCTGATTTAACATTCGCACTTGTGTCCTTTTTTAATTTTTTGGCAATTCT ACTTCTCCTTCTCCAGCTGATTTAACATTCGCGCTTGTGTCCTTTTTTAATTTTTTGGCAATTCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr5:64804281..64804381 32194978 MeRIP-seq:(Medium) rs753811241 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114862 RMVar_ID_114862 Human_SNP_ID_862050638 m1A Human chr5 + 141636442 141636442 141636442 GGTACTCCTGGTGACTTCTATCCAGCTCCCCGATACTCTAGGGGCGGGTCGCACTTCATGCACTC GGTACTCCTGGTGACTTCTATCCAGCTCCCCGGTACTCTAGGGGCGGGTCGCACTTCATGCACTC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:141636439..141636538 26863196 MeRIP-seq:(Medium) rs116972968 Functional Loss SNV ICGC 33..33 33 LAML 1 - 114863 RMVar_ID_114863 Human_SNP_ID_862052866 m1A Human chr5 + 140664952 140664952 140664952 GCACTTGTGAGGAGAGGCCCGCTGAGGATGGGAGCGACGAGGAGGACCCAGACTCCATGGAAGCC GCACTTGTGAGGAGAGGCCCGCTGAGGATGGGGGCGACGAGGAGGACCCAGACTCCATGGAAGCC A G WDR55 Ensembl:ENSG00000120314 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:140664903..140665034 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_4813486,Human_RBP_ID_23050287 114864 RMVar_ID_114864 Human_SNP_ID_862074909 m1A Human chr5 + 168467891 168467891 168467891 ACAAGGGTGAGCTTCAGACAGACAAGATGATGAGGGCAGCTGCCAAGGATGTGCACAGGCTCCGA ACAAGGGTGAGCTTCAGACAGACAAGATGATGGGGGCAGCTGCCAAGGATGTGCACAGGCTCCGA A G WWC1 Ensembl:ENSG00000113645 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr5:168467784..168467925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_78013,Human_RBP_ID_636972 Human_Splice_Rec_718368,Human_Splice_Rec_718369,Human_Splice_Rec_718412,Human_Splice_Rec_718413,Human_Splice_Rec_718470,Human_Splice_Rec_718471,Human_Splice_Rec_718520,Human_Splice_Rec_718521,Human_Splice_Rec_718554,Human_Splice_Rec_718555,Human_Splice_Rec_718570,Human_Splice_Rec_718572,Human_Splice_Rec_718573,Human_Splice_Rec_718575 RMVar_hsa_circ_268954,RMVar_hsa_circ_11114,RMVar_hsa_circ_236004 114865 RMVar_ID_114865 Human_SNP_ID_862093220 m1A Human chr5 + 169883651 169883651 169883651 TGCGAAAGCCCCCTGCCTTCTGGGACCTGGGGAAGGAGAGCGAGTAGGTGGGGGGAAGATGGTGC TGCGAAAGCCCCCTGCCTTCTGGGACCTGGGGTAGGAGAGCGAGTAGGTGGGGGGAAGATGGTGC A T DOCK2 Ensembl:ENSG00000134516 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:169883553..169883781 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin basal_cell_carcinoma 3 skin RMVar_hsa_circ_236106,RMVar_hsa_circ_107698,RMVar_hsa_circ_99424,RMVar_hsa_circ_236115,RMVar_hsa_circ_82482,RMVar_hsa_circ_87451,RMVar_hsa_circ_98887,RMVar_hsa_circ_236121,RMVar_hsa_circ_119252,RMVar_hsa_circ_95210,RMVar_hsa_circ_236124,RMVar_hsa_circ_76782,RMVar_hsa_circ_236126,RMVar_hsa_circ_236125,RMVar_hsa_circ_236122,RMVar_hsa_circ_236123 114866 RMVar_ID_114866 Human_SNP_ID_862099950 m1A Human chr5 - 172768814 172768814 172768814 CTTCCCCGTCTCCATCCCTGTCCACTCCACGAACAGTGCGCTGAGCTACCTTCAGAGCCCCATTA CTTCCCCGTCTCCATCCCTGTCCACTCCACGAGCAGTGCGCTGAGCTACCTTCAGAGCCCCATTA T C DUSP1 Ensembl:ENSG00000120129 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:172768776..172768825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_250025,Human_RBP_ID_7416763,Human_RBP_ID_8610163,Human_RBP_ID_26524495,Human_RBP_ID_27513795 RMVar_hsa_circ_236259,RMVar_hsa_circ_96412,RMVar_hsa_circ_118634,RMVar_hsa_circ_236260 114867 RMVar_ID_114867 Human_SNP_ID_862156625 m1A Human chr5 + 256391 256391 256391 TCGACAAAACTTTGAACGAGGCTGACTGTGCCACCGTCCCGCCAGCCATTCGCTCCTACTGATGA TCGACAAAACTTTGAACGAGGCTGACTGTGCCCCCGTCCCGCCAGCCATTCGCTCCTACTGATGA A C SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr5:256286..256595;chr5:256300..256417 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 4 lung Human_RBP_ID_787464,Human_RBP_ID_5151233,Human_RBP_ID_5242465,Human_RBP_ID_9175769,Human_RBP_ID_9306377,Human_RBP_ID_21900894,Human_RBP_ID_22458787,Human_RBP_ID_26525739,Human_RBP_ID_26771607 Human_Splice_Rec_630744,Human_Splice_Rec_630768,Human_Splice_Rec_630822,Human_Splice_Rec_630850,Human_Splice_Rec_630896,Human_Splice_Rec_630920,Human_Splice_Rec_630930,Human_Splice_Rec_630936,Human_Splice_Rec_630940,Human_Splice_Rec_630948,Human_Splice_Rec_630954,Human_Splice_Rec_630960,Human_Splice_Rec_630986,Human_Splice_Rec_630987 Human_miRNA_ID_833372 RMVar_hsa_circ_107608,RMVar_hsa_circ_229936,RMVar_hsa_circ_229941,RMVar_hsa_circ_378868 114868 RMVar_ID_114868 Human_SNP_ID_862157015 m1A Human chr5 + 168519199 168519199 168519199 ATAAAACCTGTCCAAAGGATGTAATCCTTCATAGGTTTGAACACTGTGTGTTTTTACCAAAGTGG ATAAAACCTGTCCAAAGGATGTAATCCTTCATGGGTTTGAACACTGTGTGTTTTTACCAAAGTGG A G RARS1 Ensembl:ENSG00000113643 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr5:168519149..168519249 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1649592,Human_RBP_ID_1991722,Human_RBP_ID_2914095,Human_RBP_ID_3764425,Human_RBP_ID_4821410,Human_RBP_ID_22460314,Human_RBP_ID_24094882 RMVar_hsa_circ_90623,RMVar_hsa_circ_236025,RMVar_hsa_circ_79536,RMVar_hsa_circ_96588,RMVar_hsa_circ_103677,RMVar_hsa_circ_236026,RMVar_hsa_circ_236029,RMVar_hsa_circ_127973,RMVar_hsa_circ_236038,RMVar_hsa_circ_236040,RMVar_hsa_circ_108533,RMVar_hsa_circ_236039,RMVar_hsa_circ_76163,RMVar_hsa_circ_236045 114869 RMVar_ID_114869 Human_SNP_ID_862169321 m1A Human chr5 + 223531 223531 223531 AACAGGAACCCGAGGTTTTCACTTCACTGTTGATGGGAACAAGAGGGCATCTGCTAAAGTTTCAG AACAGGAACCCGAGGTTTTCACTTCACTGTTGTTGGGAACAAGAGGGCATCTGCTAAAGTTTCAG A T SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:223476..223550 26863196 MeRIP-seq:(Medium) rs34635677 Functional Loss SNV COSMIC 33..33 33 ovary mucinous_carcinoma,ovary serous_carcinoma 8 ovary Human_RBP_ID_73831,Human_RBP_ID_249827,Human_RBP_ID_946525,Human_RBP_ID_1653069,Human_RBP_ID_1994063,Human_RBP_ID_2923380,Human_RBP_ID_4846268,Human_RBP_ID_5610777,Human_RBP_ID_8943824,Human_RBP_ID_18056690,Human_RBP_ID_18840898,Human_RBP_ID_22459468 Human_Splice_Rec_630724,Human_Splice_Rec_630725,Human_Splice_Rec_630746,Human_Splice_Rec_630747,Human_Splice_Rec_630770,Human_Splice_Rec_630771,Human_Splice_Rec_630774,Human_Splice_Rec_630775,Human_Splice_Rec_630798,Human_Splice_Rec_630799,Human_Splice_Rec_630824,Human_Splice_Rec_630825,Human_Splice_Rec_630854,Human_Splice_Rec_630855,Human_Splice_Rec_630860,Human_Splice_Rec_630861,Human_Splice_Rec_630962,Human_Splice_Rec_630963 Human_miRNA_ID_2586457 Clinvar_Rec_146 GWAS_ID_6658 RMVar_hsa_circ_47809,RMVar_hsa_circ_318776,RMVar_hsa_circ_375563,RMVar_hsa_circ_347448,RMVar_hsa_circ_92161,RMVar_hsa_circ_229931,RMVar_hsa_circ_229932,RMVar_hsa_circ_229933,RMVar_hsa_circ_229930 114870 RMVar_ID_114870 Human_SNP_ID_862188887 m1A Human chr5 - 135033769 135033769 135033769 GGGGCCCGCCTTCCACCTGGCCCGGCCCGCCGACCCCCGCGAGCCGCTCGAGAACTCCGCCAGCG GGGGCCCGCCTTCCACCTGGCCCGGCCCGCCGCCCCCCGCGAGCCGCTCGAGAACTCCGCCAGCG T G PITX1 Ensembl:ENSG00000069011 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr5:135033726..135033995 26863196 MeRIP-seq:(Medium) rs1044912477 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_24083974,Human_RBP_ID_26826543 Human_Splice_Rec_693659,Human_Splice_Rec_693665,Human_Splice_Rec_693677,Human_Splice_Rec_693681 RMVar_hsa_circ_86064,RMVar_hsa_circ_234632 114871 RMVar_ID_114871 Human_SNP_ID_862228603 m1A Human chr5 - 44809011 44809011 44809011 CGTGGCGGCGGCATTAGCCGCGGTGTGCAATGAAAGCCTCGGACCGCGTAGCAAAGGCCTCCAAC CGTGGCGGCGGCATTAGCCGCGGTGTGCAATGTAAGCCTCGGACCGCGTAGCAAAGGCCTCCAAC T A MRPS30-DT,MRPS30-DT:2,MRPS30-DT:3,MRPS30-DT:4,MRPS30-DT:5,MRPS30-DT:6,MRPS30-DT:7,MRPS30-DT:8,MRPS30-DT:9,MRPS30-DT:10 RNACentral:URS0000D5BF6F,RNACentral:URS0000D5BBD7,RNACentral:URS00009BB9BA,RNACentral:URS00008B5F3B,RNACentral:URS0000D59BFB,RNACentral:URS0000D5B3EF,RNACentral:URS00008C1D2C,RNACentral:URS0000D572DF,RNACentral:URS0000D5D17D,RNACentral:URS0000D5D0FD lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron,intron,exon,exon,exon,exon,exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr5:44808951..44809171 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114872 RMVar_ID_114872 Human_SNP_ID_862237890 m1A Human chr5 - 126583980 126583980 126583980 ATTCCTGCTCCAAAACGAGGAGAAATAGTAAGACAGATTGGCGATGCCTTGCGGGAGAAGATCCA ATTCCTGCTCCAAAACGAGGAGAAATAGTAAGGCAGATTGGCGATGCCTTGCGGGAGAAGATCCA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:126583910..126584063 26863196 MeRIP-seq:(Medium) rs762428797 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_76543,Human_RBP_ID_4806183,Human_RBP_ID_15279554 Human_Splice_Rec_685870,Human_Splice_Rec_685871,Human_Splice_Rec_685904,Human_Splice_Rec_685905,Human_Splice_Rec_685938,Human_Splice_Rec_685939,Human_Splice_Rec_685974,Human_Splice_Rec_685975,Human_Splice_Rec_686008,Human_Splice_Rec_686009,Human_Splice_Rec_686038,Human_Splice_Rec_686039,Human_Splice_Rec_686100,Human_Splice_Rec_686101,Human_Splice_Rec_686136,Human_Splice_Rec_686137,Human_Splice_Rec_686166,Human_Splice_Rec_686167,Human_Splice_Rec_686200,Human_Splice_Rec_686201,Human_Splice_Rec_686278,Human_Splice_Rec_686279,Human_Splice_Rec_686307,Human_Splice_Rec_686338,Human_Splice_Rec_686339,Human_Splice_Rec_686366,Human_Splice_Rec_686367,Human_Splice_Rec_686400,Human_Splice_Rec_686401,Human_Splice_Rec_686434,Human_Splice_Rec_686435,Human_Splice_Rec_686484,Human_Splice_Rec_686485,Human_Splice_Rec_686522,Human_Splice_Rec_686523,Human_Splice_Rec_686548,Human_Splice_Rec_686549,Human_Splice_Rec_686578,Human_Splice_Rec_686579,Human_Splice_Rec_686586,Human_Splice_Rec_686587,Human_Splice_Rec_686596,Human_Splice_Rec_686597,Human_Splice_Rec_686601,Human_Splice_Rec_686608,Human_Splice_Rec_686609 RMVar_hsa_circ_344614,RMVar_hsa_circ_265700,RMVar_hsa_circ_37348,RMVar_hsa_circ_359337,RMVar_hsa_circ_15190,RMVar_hsa_circ_72210,RMVar_hsa_circ_29976,RMVar_hsa_circ_16646,RMVar_hsa_circ_58007,RMVar_hsa_circ_370455,RMVar_hsa_circ_329082,RMVar_hsa_circ_234074,RMVar_hsa_circ_234073,RMVar_hsa_circ_234079,RMVar_hsa_circ_114609,RMVar_hsa_circ_350153,RMVar_hsa_circ_311131,RMVar_hsa_circ_346998,RMVar_hsa_circ_234075,RMVar_hsa_circ_301951,RMVar_hsa_circ_14822,RMVar_hsa_circ_234080,RMVar_hsa_circ_234081,RMVar_hsa_circ_288361,RMVar_hsa_circ_297396,RMVar_hsa_circ_234083,RMVar_hsa_circ_234084,RMVar_hsa_circ_292118,RMVar_hsa_circ_338467,RMVar_hsa_circ_234085,RMVar_hsa_circ_318307,RMVar_hsa_circ_374884,RMVar_hsa_circ_310944 114873 RMVar_ID_114873 Human_SNP_ID_862252714 m1A Human chr5 + 138467061 138467061 138467061 GTGCCATCCAACGACAGCAGTCCCATTTACTCAGCGGCACCCACCTTCCCCACGCCGAACACTGA GTGCCATCCAACGACAGCAGTCCCATTTACTCCGCGGCACCCACCTTCCCCACGCCGAACACTGA A C EGR1 Ensembl:ENSG00000120738 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr5:138466874..138467189 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4849987,Human_RBP_ID_17303450,Human_RBP_ID_17415583,Human_RBP_ID_22099663,Human_RBP_ID_26351342,Human_RBP_ID_27511757,Human_RBP_ID_27826805 114874 RMVar_ID_114874 Human_SNP_ID_862269402 m1A Human chr5 + 180293333 180293333 180293333 GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGAGAGGCACTGAGGCTGGGCACATGGGGAAAACC GCCAGATCTACGTTGAAAAGTGAAGCAGGAAGGGAGGCACTGAGGCTGGGCACATGGGGAAAACC A G AC008610.1 Ensembl:ENSG00000248367 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:180293282..180293556 26863196 MeRIP-seq:(Medium) rs75469971 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5615028 Human_Splice_Rec_731121 114875 RMVar_ID_114875 Human_SNP_ID_862270787 m1A Human chr5 - 179833577 179833577 179833577 CAGTTATCCGACTCCATCTGTTCCTGGAACAAAACTCACCATGAGCACACAGGAGACACGCGCAA CAGTTATCCGACTCCATCTGTTCCTGGAACAAGACTCACCATGAGCACACAGGAGACACGCGCAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr5:179833576..179833625;chr5:179833576..179833650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_639853 114876 RMVar_ID_114876 Human_SNP_ID_862274131 m1A Human chr5 + 112922185 112922185 112922185 AGGAACCGGTCGAACCTCTCCCTCATGGCCGCAGACATGGCGGGGACCGTCTCGCCGCTCGGGGC AGGAACCGGTCGAACCTCTCCCTCATGGCCGCCGACATGGCGGGGACCGTCTCGCCGCTCGGGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr5:112922076..112922300;chr5:112922136..112922270 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain 114877 RMVar_ID_114877 Human_SNP_ID_862282896 m1A Human chr5 - 128537912 128537912 128537912 AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGACGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG AGGGCTTTTGTAATTTCCTCCCCCGCCCGCTGGCGGTCCTGGAGTCGCTCGGGGCTTTAGGCCGG T C FBN2 Ensembl:ENSG00000138829 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7732639 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_5476173 Clinvar_Rec_674 GWAS_ID_14069 RMVar_hsa_circ_99795,RMVar_hsa_circ_234187 114878 RMVar_ID_114878 Human_SNP_ID_862303453 m1A Human chr5 - 138557363 138557363 138557363 ACTTCTTGTCTTCTGAACTTTAATCTTAGTAAAGCTCAGTCTTGACAGTGGGAGTTTGGGGCTGG ACTTCTTGTCTTCTGAACTTTAATCTTAGTAAGGCTCAGTCTTGACAGTGGGAGTTTGGGGCTGG T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr5:138557360..138557522 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_1645621,Human_RBP_ID_1987826,Human_RBP_ID_2898357,Human_RBP_ID_5213984,Human_RBP_ID_18833488,Human_RBP_ID_22481810,Human_RBP_ID_24503713 RMVar_hsa_circ_64990,RMVar_hsa_circ_91150,RMVar_hsa_circ_234833 114879 RMVar_ID_114879 Human_SNP_ID_862304216 m1A Human chr5 - 10748269 10748269 10748269 TTAATCCCACACTCTCTGTTTTCATTTCAGTGAAAGCTGGTGGAATGCGAATTGTGCAGAAACAC TTAATCCCACACTCTCTGTTTTCATTTCAGTGTAAGCTGGTGGAATGCGAATTGTGCAGAAACAC T A DAP Ensembl:ENSG00000112977 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr5:10748226..10748333 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_628002,Human_RBP_ID_4803018,Human_RBP_ID_9397643,Human_RBP_ID_17415144,Human_RBP_ID_22459507,Human_RBP_ID_26827038 Human_Splice_Rec_635434,Human_Splice_Rec_635435,Human_Splice_Rec_635440,Human_Splice_Rec_635441,Human_Splice_Rec_635444,Human_Splice_Rec_635445,Human_Splice_Rec_635450,Human_Splice_Rec_635451,Human_Splice_Rec_635454,Human_Splice_Rec_635455,Human_Splice_Rec_635458 RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 114880 RMVar_ID_114880 Human_SNP_ID_867148494 m1A Human chr7 + 50445835 50445835 50445835 AGCTGGTTGCTGACACCTTGCAACAGCAAACAATGCACGGACCATTTTCTCCCCCTCACCTACCC AGCTGGTTGCTGACACCTTGCAACAGCAAACAGTGCACGGACCATTTTCTCCCCCTCACCTACCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:50445786..50445881 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 114881 RMVar_ID_114881 Human_SNP_ID_867155654 m1A Human chr7 + 893781 893781 893781 GACGGTGTTCACTGTGCTGTGTGAGCAGTACCAGCCATCCCTCCGGCGGGACCCCATGTACAACG GACGGTGTTCACTGTGCTGTGTGAGCAGTACCGGCCATCCCTCCGGCGGGACCCCATGTACAACG A G GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:886102..896037 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_793773,Human_RBP_ID_954040,Human_RBP_ID_5243182,Human_RBP_ID_9311106,Human_RBP_ID_18413922,Human_RBP_ID_19020384,Human_RBP_ID_19134478 Human_Splice_Rec_836870,Human_Splice_Rec_836871,Human_Splice_Rec_836910,Human_Splice_Rec_836911,Human_Splice_Rec_836932,Human_Splice_Rec_836933,Human_Splice_Rec_836952 RMVar_hsa_circ_1094,RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239,RMVar_hsa_circ_373973,RMVar_hsa_circ_243243 114882 RMVar_ID_114882 Human_SNP_ID_867162458 m1A Human chr7 - 102538297 102538296 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACT_TTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC AT A POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs201449870 Functional Loss DEL ICGC 33..33 33 PRAD 1 - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 114883 RMVar_ID_114883 Human_SNP_ID_867163545 m1A Human chr7 - 75528018 75528018 75528018 GAGCATCGCATAGCCTGCGGGGCTGGATGCTGACCGCCCGGGCCAGCACCTAGGCGGACGCGGAG GAGCATCGCATAGCCTGCGGGGCTGGATGCTGTCCGCCCGGGCCAGCACCTAGGCGGACGCGGAG T A PMS2P3 Ensembl:ENSG00000127957 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:75527950..75528049 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4956423,Human_RBP_ID_5328481,Human_RBP_ID_5623503,Human_RBP_ID_17166888,Human_RBP_ID_17672233,Human_RBP_ID_18426353,Human_RBP_ID_23080080 114884 RMVar_ID_114884 Human_SNP_ID_867176974 m1A Human chr7 + 123692767 123692767 123692767 GCTGTGGGAGCTCTTGAAGGTGGTGGGGGAGGAGCGCCTCTTCCCCTAGCAGGAGGAGGAGGAGG GCTGTGGGAGCTCTTGAAGGTGGTGGGGGAGGTGCGCCTCTTCCCCTAGCAGGAGGAGGAGGAGG A T - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:123692676..123692800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114885 RMVar_ID_114885 Human_SNP_ID_867179525 m1A Human chr7 - 588733 588728 588734 CCACCATCACCATCACCATCACCACTGTCACTATCCTCACCACCATCACCACCATCACCATCACC CCACCATCACCATCACCATCACCACTGTCAC______CACCACCATCACCACCATCACCATCACC GAGGATA G PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:588731..589037 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..37 33 NKTL 1 - RMVar_hsa_circ_13819,RMVar_hsa_circ_109563,RMVar_hsa_circ_302771,RMVar_hsa_circ_342825,RMVar_hsa_circ_276511,RMVar_hsa_circ_243184,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_243185,RMVar_hsa_circ_337394 114886 RMVar_ID_114886 Human_SNP_ID_867193944 m1A Human chr7 + 1477924 1477924 1477924 GCTCCTCCAGGTGGGGGGACCTCACCTCGATCAGCCCCTGGAGGACTGCGCAAGGGACAAAGAGA GCTCCTCCAGGTGGGGGGACCTCACCTCGATCGGCCCCTGGAGGACTGCGCAAGGGACAAAGAGA A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1477873..1477945 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 114887 RMVar_ID_114887 Human_SNP_ID_867225389 m1A Human chr7 - 5529623 5529623 5529623 GGATGATGATATCGCCGCGCTCGTCGTCGACAACGGCTCCGGCATGTGCAAGGCCGGCTTCGCGG GGATGATGATATCGCCGCGCTCGTCGTCGACAGCGGCTCCGGCATGTGCAAGGCCGGCTTCGCGG T C ACTB Ensembl:ENSG00000075624 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5529101..5529773 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_686016,Human_RBP_ID_1052537,Human_RBP_ID_1687666,Human_RBP_ID_2044288,Human_RBP_ID_3848754,Human_RBP_ID_4945009,Human_RBP_ID_5219392,Human_RBP_ID_5429647,Human_RBP_ID_5513496,Human_RBP_ID_7746281,Human_RBP_ID_8669093,Human_RBP_ID_8911997,Human_RBP_ID_9337009,Human_RBP_ID_16179247,Human_RBP_ID_17541777,Human_RBP_ID_18211597,Human_RBP_ID_18883967,Human_RBP_ID_22463008,Human_RBP_ID_22534238,Human_RBP_ID_24219618,Human_RBP_ID_24438466,Human_RBP_ID_26552364,Human_RBP_ID_26830149,Human_RBP_ID_27114857,Human_RBP_ID_27161799,Human_RBP_ID_27532666 Human_Splice_Rec_840812,Human_Splice_Rec_840813,Human_Splice_Rec_840826,Human_Splice_Rec_840827,Human_Splice_Rec_840838,Human_Splice_Rec_840839,Human_Splice_Rec_840847,Human_Splice_Rec_840862,Human_Splice_Rec_840863,Human_Splice_Rec_840874,Human_Splice_Rec_840877,Human_Splice_Rec_840882,Human_Splice_Rec_840883,Human_Splice_Rec_840889,Human_Splice_Rec_840896,Human_Splice_Rec_840897,Human_Splice_Rec_840902,Human_Splice_Rec_840904,Human_Splice_Rec_840905,Human_Splice_Rec_840908,Human_Splice_Rec_840909,Human_Splice_Rec_840914,Human_Splice_Rec_840915 RMVar_hsa_circ_110714,RMVar_hsa_circ_126855,RMVar_hsa_circ_243503,RMVar_hsa_circ_243504,RMVar_hsa_circ_105019,RMVar_hsa_circ_88728,RMVar_hsa_circ_123677,RMVar_hsa_circ_243511,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243514,RMVar_hsa_circ_373642,RMVar_hsa_circ_243516,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 114888 RMVar_ID_114888 Human_SNP_ID_867231211 m1A Human chr7 - 32975288 32975288 32975288 ACAAAATCAGACACCTGGATGGTCCGAGGGCAACTCGGGGGCTTGAAATAGGTGTGAATCTGAAC ACAAAATCAGACACCTGGATGGTCCGAGGGCACCTCGGGGGCTTGAAATAGGTGTGAATCTGAAC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:32975237..32975337 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 114889 RMVar_ID_114889 Human_SNP_ID_867239160 m1A Human chr7 + 51316715 51316715 51316715 CGCTGGCTACCGCCGCCACCGCTGCCGCCCTCATTCACTTTTTCCGCGCTGACCCATCGTCCTCC CGCTGGCTACCGCCGCCACCGCTGCCGCCCTCGTTCACTTTTTCCGCGCTGACCCATCGTCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:51316561..51316823;chr7:51316576..51316800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 114890 RMVar_ID_114890 Human_SNP_ID_867255912 m1A Human chr7 + 102227481 102227481 102227481 CGAGCTGGTCCAGCAGCCCTGTCCCCCCATCGAGGCGAGCAAGGACAGCAAGCCACCAGAGCCCA CGAGCTGGTCCAGCAGCCCTGTCCCCCCATCGGGGCGAGCAAGGACAGCAAGCCACCAGAGCCCA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:102227432..102227586 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 16 lung Human_RBP_ID_5153423 RMVar_hsa_circ_247268,RMVar_hsa_circ_85687,RMVar_hsa_circ_116650,RMVar_hsa_circ_120785,RMVar_hsa_circ_247267,RMVar_hsa_circ_247269,RMVar_hsa_circ_107883,RMVar_hsa_circ_65091,RMVar_hsa_circ_247279,RMVar_hsa_circ_378451,RMVar_hsa_circ_65716,RMVar_hsa_circ_103768,RMVar_hsa_circ_267024,RMVar_hsa_circ_80446,RMVar_hsa_circ_247283,RMVar_hsa_circ_264945,RMVar_hsa_circ_87029,RMVar_hsa_circ_266127,RMVar_hsa_circ_332701,RMVar_hsa_circ_247285,RMVar_hsa_circ_286520,RMVar_hsa_circ_247286,RMVar_hsa_circ_247287,RMVar_hsa_circ_247288,RMVar_hsa_circ_247289 114891 RMVar_ID_114891 Human_SNP_ID_867316159 m1A Human chr7 - 4785676 4785676 4785676 AGCGCCACCCCACCCTGGGCTCACCGTGGCTCAGGAAGAAGTGGGCGAGGGGCAGCAGCACCCGC AGCGCCACCCCACCCTGGGCTCACCGTGGCTCTGGAAGAAGTGGGCGAGGGGCAGCAGCACCCGC T A RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:4784255..4785675 32194978 MeRIP-seq:(Medium) rs11772411 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma 2 large intestine Clinvar_Rec_679 114892 RMVar_ID_114892 Human_SNP_ID_867322168 m1A Human chr7 + 55953187 55953187 55953187 GAGACTTTGGAATTTGCTTTTCAGGTGACCAAAGCCACGTAATGTCCGTAGTTCGCTCATCCGTC GAGACTTTGGAATTTGCTTTTCAGGTGACCAATGCCACGTAATGTCCGTAGTTCGCTCATCCGTC A T AC092647.5,MRPS17,NIPSNAP2 Ensembl:ENSG00000249773,Ensembl:ENSG00000239789,Ensembl:ENSG00000146729 Protein coding,Protein coding,Protein coding CDS,5'UTR,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:55951842..55964691 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_686040,Human_RBP_ID_954448,Human_RBP_ID_1687680,Human_RBP_ID_4956355 Human_Splice_Rec_868672,Human_Splice_Rec_868842,Human_Splice_Rec_868846 Human_miRNA_ID_2417180,Human_miRNA_ID_3106893 RMVar_hsa_circ_114624,RMVar_hsa_circ_245195 114893 RMVar_ID_114893 Human_SNP_ID_867331182 m1A Human chr7 - 43788007 43788007 43788007 ACATTGTGAGCCACCTCGACACGAAGCCAATCAGGTTCAGGAACGCTGAGGAAGGGTGTGGATTC ACATTGTGAGCCACCTCGACACGAAGCCAATCTGGTTCAGGAACGCTGAGGAAGGGTGTGGATTC T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:43787901..43791270 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung mixed_adenosquamous_carcinoma 2 lung 114894 RMVar_ID_114894 Human_SNP_ID_867334769 m1A Human chr7 - 135362923 135362923 135362923 AGACAGCCTTCAGACCCCCCAGCAAAACCCCCACAGATTTACTACAGAGTTCAACACTGGACCGC AGACAGCCTTCAGACCCCCCAGCAAAACCCCCCCAGATTTACTACAGAGTTCAACACTGGACCGC T G CNOT4 Ensembl:ENSG00000080802 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:135362874..135362982 26863196 MeRIP-seq:(Medium) rs1219674854 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_18960433 114895 RMVar_ID_114895 Human_SNP_ID_867345437 m1A Human chr7 - 76329570 76329570 76329570 ACGATGGCGGCGAAGGCAACAATTAAGGCCCCAGGGGAACTGGCAGCGCACGCGGATGCTACTAC ACGATGGCGGCGAAGGCAACAATTAAGGCCCCGGGGGAACTGGCAGCGCACGCGGATGCTACTAC T C YWHAG Ensembl:ENSG00000170027 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76329351..76329750 26863196 MeRIP-seq:(Medium) rs745551920 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1052956,Human_RBP_ID_4949429,Human_RBP_ID_7758416,Human_RBP_ID_9404593,Human_RBP_ID_16221649,Human_RBP_ID_18104157,Human_RBP_ID_22110880,Human_RBP_ID_22463161 Human_miRNA_ID_2436412,Human_miRNA_ID_2436413,Human_miRNA_ID_2436414 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821,RMVar_hsa_circ_87415,RMVar_hsa_circ_245820,RMVar_hsa_circ_245826 114896 RMVar_ID_114896 Human_SNP_ID_867348739 m1A Human chr7 + 32988626 32988621 32988626 TGGAGAAAAGCGAAGGATTGTGGTCCCGCCTCACCTGGGGTATGGAGAGGAAGGAAGAGGTGAGC TGGAGAAAAGCGAAGGATTGTGGTCCCG_____CCTGGGGTATGGAGAGGAAGGAAGAGGTGAGC GCCTCA G FKBP9 Ensembl:ENSG00000122642 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:32988601..32988625 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 29..33 33 BRCA 1 - Human_RBP_ID_957265,Human_RBP_ID_7733480,Human_RBP_ID_9354747,Human_RBP_ID_22774870,Human_RBP_ID_24212415 Human_Splice_Rec_855227,Human_Splice_Rec_855259,Human_Splice_Rec_855279,Human_Splice_Rec_855285,Human_Splice_Rec_855291,Human_Splice_Rec_855299,Human_Splice_Rec_855309,Human_Splice_Rec_855311 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430,RMVar_hsa_circ_40351,RMVar_hsa_circ_58345,RMVar_hsa_circ_306923,RMVar_hsa_circ_340938,RMVar_hsa_circ_244487,RMVar_hsa_circ_95462,RMVar_hsa_circ_360172,RMVar_hsa_circ_244488,RMVar_hsa_circ_41139,RMVar_hsa_circ_244490,RMVar_hsa_circ_93439,RMVar_hsa_circ_278686,RMVar_hsa_circ_334124,RMVar_hsa_circ_374182,RMVar_hsa_circ_103038,RMVar_hsa_circ_244491,RMVar_hsa_circ_244492,RMVar_hsa_circ_244489 114897 RMVar_ID_114897 Human_SNP_ID_867356605 m1A Human chr7 + 131511376 131511376 131511376 TCTGCTGGGCTGTATCTGTAGCCATGATGGTGACACTGGATGCTGGAGTCGGTGCTGTTTTGTTA TCTGCTGGGCTGTATCTGTAGCCATGATGGTGGCACTGGATGCTGGAGTCGGTGCTGTTTTGTTA A G RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:131511326..131511456 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 114898 RMVar_ID_114898 Human_SNP_ID_867372400 m1A Human chr7 + 155737547 155737547 155737547 GTTGTTGTTCTTTAGGGCCCTCCAGAATTTCCACAGCATACACCTGGACCTGTTCCCAACAGTTT GTTGTTGTTCTTTAGGGCCCTCCAGAATTTCCGCAGCATACACCTGGACCTGTTCCCAACAGTTT A G RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155737520..155737602 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary Human_RBP_ID_85627,Human_RBP_ID_955150,Human_RBP_ID_8662639,Human_RBP_ID_9405053,Human_RBP_ID_16083947,Human_RBP_ID_22686175,Human_RBP_ID_26132408,Human_RBP_ID_26357406 Human_Splice_Rec_942032,Human_Splice_Rec_942076,Human_Splice_Rec_942092,Human_Splice_Rec_942100 RMVar_hsa_circ_124662,RMVar_hsa_circ_120729,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_358134,RMVar_hsa_circ_363833,RMVar_hsa_circ_42301,RMVar_hsa_circ_72053,RMVar_hsa_circ_125145,RMVar_hsa_circ_126622,RMVar_hsa_circ_368148,RMVar_hsa_circ_112913,RMVar_hsa_circ_80095,RMVar_hsa_circ_82952,RMVar_hsa_circ_77184,RMVar_hsa_circ_249696,RMVar_hsa_circ_249698,RMVar_hsa_circ_249700,RMVar_hsa_circ_249701,RMVar_hsa_circ_249699,RMVar_hsa_circ_249697,RMVar_hsa_circ_249703,RMVar_hsa_circ_118858,RMVar_hsa_circ_123050,RMVar_hsa_circ_249704,RMVar_hsa_circ_25886,RMVar_hsa_circ_321738,RMVar_hsa_circ_342357,RMVar_hsa_circ_249705 114899 RMVar_ID_114899 Human_SNP_ID_867402199 m1A Human chr7 - 45252018 45252018 45252018 ACAGGCGGGGTAAGATTTGCCGAGTTCCTTTTACTTTTTTTAACCTTTCCTTATAAGCATGCCTG ACAGGCGGGGTAAGATTTGCCGAGTTCCTTTTTCTTTTTTTAACCTTTCCTTATAAGCATGCCTG T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:45251950..45252066 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114900 RMVar_ID_114900 Human_SNP_ID_867416465 m1A Human chr7 - 1010058 1010058 1010058 GGAGCAGAGGGTCCTGGAAAGGAAGCTGAAAAAGGAACGGAAGAAAGAGGAGAGGCAGCGTCTGC GGAGCAGAGGGTCCTGGAAAGGAAGCTGAAAAGGGAACGGAAGAAAGAGGAGAGGCAGCGTCTGC T C C7orf50 Ensembl:ENSG00000146540 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_672326,Human_RBP_ID_4957604,Human_RBP_ID_5122971,Human_RBP_ID_8944138,Human_RBP_ID_19019361,Human_RBP_ID_26357482,Human_RBP_ID_26550253 Human_Splice_Rec_837272,Human_Splice_Rec_837280,Human_Splice_Rec_837288,Human_Splice_Rec_837294,Human_Splice_Rec_837302,Human_Splice_Rec_837308,Human_Splice_Rec_837316 RMVar_hsa_circ_357195,RMVar_hsa_circ_1847,RMVar_hsa_circ_51160,RMVar_hsa_circ_377843 114901 RMVar_ID_114901 Human_SNP_ID_867429958 m1A Human chr7 + 151126289 151126274 151126289 GTGCGGAGACCCCTTCCCGCCCTGACTGTCGGAGAAACCGCGCGCAGTGCAGGCCTTGAGGGGCT GTGCGGAGACCCCTTCCC_______________GAAACCGCGCGCAGTGCAGGCCTTGAGGGGCT CGCCCTGACTGTCGGA C AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:151126283..151126351 26863196 MeRIP-seq:(Medium) rs141643830 Functional Loss DEL ICGC 19..33 33 PEME 1 - Human_RBP_ID_18426466,Human_RBP_ID_22703850,Human_RBP_ID_24388914 RMVar_hsa_circ_113536,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425,RMVar_hsa_circ_303719,RMVar_hsa_circ_367215,RMVar_hsa_circ_249427,RMVar_hsa_circ_108214,RMVar_hsa_circ_249429,RMVar_hsa_circ_85613,RMVar_hsa_circ_249430,RMVar_hsa_circ_3325,RMVar_hsa_circ_249434,RMVar_hsa_circ_249432,RMVar_hsa_circ_357571,RMVar_hsa_circ_375169,RMVar_hsa_circ_352425,RMVar_hsa_circ_249433,RMVar_hsa_circ_85626,RMVar_hsa_circ_331841,RMVar_hsa_circ_249439 114902 RMVar_ID_114902 Human_SNP_ID_867435373 m1A Human chr7 + 74376241 74376240 74376241 CCAGCGAGAACATGGGGCTAATGGACAACTGGAAATCCAAGCTGGACTCGCTGGCCTCGGACCAC CCAGCGAGAACATGGGGCTAATGGACAACTGG_AATCCAAGCTGGACTCGCTGGCCTCGGACCAC GA G CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:74360274..74376463 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 KIRP 1 - Human_RBP_ID_174347 RMVar_hsa_circ_107546,RMVar_hsa_circ_2528,RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_83371,RMVar_hsa_circ_245672,RMVar_hsa_circ_103650,RMVar_hsa_circ_245670,RMVar_hsa_circ_245679,RMVar_hsa_circ_372481,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245685,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_8106,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245693,RMVar_hsa_circ_103611,RMVar_hsa_circ_282092,RMVar_hsa_circ_313787,RMVar_hsa_circ_245694,RMVar_hsa_circ_245692 114903 RMVar_ID_114903 Human_SNP_ID_867498895 m1A Human chr7 + 141738451 141738451 141738451 GGAAGGGATAGCCAGCGCGAAGGAAGTGCTGGAGTCGTGTGTTTTGGCTGCGCGTGATCCTGCGT GGAAGGGATAGCCAGCGCGAAGGAAGTGCTGGGGTCGTGTGTTTTGGCTGCGCGTGATCCTGCGT A G SSBP1 Ensembl:ENSG00000106028 Protein coding 5'UTR GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:141738376..141738525 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_4957891,Human_RBP_ID_9337421,Human_RBP_ID_18426444,Human_RBP_ID_22833614,Human_RBP_ID_23215682,Human_RBP_ID_24197324 Human_Splice_Rec_931125,Human_Splice_Rec_931199 RMVar_hsa_circ_86085,RMVar_hsa_circ_249210 114904 RMVar_ID_114904 Human_SNP_ID_867505239 m1A Human chr7 + 7883015 7883011 7883015 GAGGAAGAAGAAGAAGGAGGAGGAGAAGGAGGAAGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GAGGAAGAAGAAGAAGGAGGAGGAGAAGG____AGAAGAAAGAAGAAGAAAGAAGAGGAAGAAGA GAGGA G AC007161.3,UMAD1 Ensembl:ENSG00000283549,Ensembl:ENSG00000219545 lincRNA,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:7882965..7883110 26863196 MeRIP-seq:(Medium) rs768344868 Functional Loss DEL ICGC 30..33 33 ESCA 1 - Human_RBP_ID_5105317 RMVar_hsa_circ_243749,RMVar_hsa_circ_243748,RMVar_hsa_circ_243750 114905 RMVar_ID_114905 Human_SNP_ID_867512819 m1A Human chr7 + 107758428 107758428 107758428 ATTCCGCCAAAGCAGCACATCATGATGCCACCACCTCCTTTGCAACATGTGCCACATGAGCACTA ATTCCGCCAAAGCAGCACATCATGATGCCACCGCCTCCTTTGCAACATGTGCCACATGAGCACTA A G CBLL1 Ensembl:ENSG00000105879 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:107758379..107758583 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 RECA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1680239,Human_RBP_ID_18088853,Human_RBP_ID_26357009 RMVar_hsa_circ_107117,RMVar_hsa_circ_247750 114906 RMVar_ID_114906 Human_SNP_ID_867521649 m1A Human chr7 - 75939267 75939266 75939268 GGCAGGCAGGCTCCTAATCCCACAGAGCTTACAGTCTGGAAAGCCTCTAGACAATGTTCAGGTAC GGCAGGCAGGCTCCTAATCCCACAGAGCTTA__GTCTGGAAAGCCTCTAGACAATGTTCAGGTAC CTG C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:75939260..75939389 26863196 MeRIP-seq:(Medium) rs1458224968 Functional Loss DEL ICGC 32..33 33 PBCA 1 - 114907 RMVar_ID_114907 Human_SNP_ID_867575623 m1A Human chr7 + 44467961 44467961 44467961 GATCGTCAAAAAGAGAACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGC GATCGTCAAAAAGAGAACCAAGAAGTTCATCCGGCACCAGTCAGACCAATATGTCAAAATTAAGC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs562719193 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,STAD,oesophagus adenocarcinoma,liver neoplasm,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 liver,oesophagus,large intestine,haematopoietic and lymphoid tissue,breast Human_miRNA_ID_1822365 114908 RMVar_ID_114908 Human_SNP_ID_867593108 m1A Human chr7 + 100586062 100586062 100586062 CCGGGCACGGAGGTCGTGGCTGCCGCCTCCTCACCCCCGGCGGCGAGTGGAGCCGCTACGGCCGC CCGGGCACGGAGGTCGTGGCTGCCGCCTCCTCCCCCCCGGCGGCGAGTGGAGCCGCTACGGCCGC A C FBXO24 Ensembl:ENSG00000106336 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100585973..100586119 26863196 MeRIP-seq:(Medium) rs746418640 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114909 RMVar_ID_114909 Human_SNP_ID_867664632 m1A Human chr7 - 99404934 99404934 99404934 CGGGTCTCTGCAGGAAGAAAGGGAGGCCACAAAGGCCGGGCGAGGCAGTATACAAGCCCTGAGGA CGGGTCTCTGCAGGAAGAAAGGGAGGCCACAATGGCCGGGCGAGGCAGTATACAAGCCCTGAGGA T A PDAP1 Ensembl:ENSG00000106244 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:99404810..99405018 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_954651,Human_RBP_ID_4956490,Human_RBP_ID_5123038,Human_RBP_ID_9403644,Human_RBP_ID_26356743,Human_RBP_ID_27829567 Human_Splice_Rec_895098,Human_Splice_Rec_895099,Human_Splice_Rec_895108,Human_Splice_Rec_895109,Human_Splice_Rec_895117,Human_Splice_Rec_895120,Human_Splice_Rec_895121 RMVar_hsa_circ_354157,RMVar_hsa_circ_246947,RMVar_hsa_circ_299942,RMVar_hsa_circ_331679,RMVar_hsa_circ_112459 114910 RMVar_ID_114910 Human_SNP_ID_867734828 m1A Human chr7 + 155208965 155208965 155208965 ATGTGAGTGTGTGTGGGAATATGTGTGTGTGTATGAGTGTGTCTGTGTGTGGGAATGGGTGTGAG ATGTGAGTGTGTGTGGGAATATGTGTGTGTGTGTGAGTGTGTCTGTGTGTGGGAATGGGTGTGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:155208666..155209045 26863196 MeRIP-seq:(Medium) rs200372460 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_24201492 114911 RMVar_ID_114911 Human_SNP_ID_867741735 m1A Human chr7 - 100678290 100678290 100678290 GCCTAGCTCGCCCCAAAACTCACAGCCACTGCATTGATGTCGGATTCATGGCCGATGAAGGTCTG GCCTAGCTCGCCCCAAAACTCACAGCCACTGCGTTGATGTCGGATTCATGGCCGATGAAGGTCTG T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100678126..100678825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 7 brain 114912 RMVar_ID_114912 Human_SNP_ID_867757798 m1A Human chr7 + 2369653 2369653 2369653 ATTGGCAGAAGAACGGAGACTACTTGTGTGTGAAAGTAGATAGGACTCCGAAAGGCACCCAGGTA ATTGGCAGAAGAACGGAGACTACTTGTGTGTGGAAGTAGATAGGACTCCGAAAGGCACCCAGGTA A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:2369552..2369653 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cervix small_cell_carcinoma 2 uterus Human_RBP_ID_83846,Human_RBP_ID_681399,Human_RBP_ID_954110,Human_RBP_ID_2040139,Human_RBP_ID_3970749,Human_RBP_ID_5223197,Human_RBP_ID_5622837,Human_RBP_ID_9311710,Human_RBP_ID_9403120,Human_RBP_ID_16119268,Human_RBP_ID_19020504,Human_RBP_ID_23116875,Human_RBP_ID_24208155,Human_RBP_ID_26356183 Human_Splice_Rec_838405,Human_Splice_Rec_838451,Human_Splice_Rec_838485 Human_miRNA_ID_2539280 RMVar_hsa_circ_9806,RMVar_hsa_circ_67893,RMVar_hsa_circ_66703,RMVar_hsa_circ_332235,RMVar_hsa_circ_48652,RMVar_hsa_circ_243330,RMVar_hsa_circ_375947,RMVar_hsa_circ_69546,RMVar_hsa_circ_243333,RMVar_hsa_circ_296863,RMVar_hsa_circ_126752,RMVar_hsa_circ_76094,RMVar_hsa_circ_243335,RMVar_hsa_circ_32145,RMVar_hsa_circ_56018,RMVar_hsa_circ_243337,RMVar_hsa_circ_243336,RMVar_hsa_circ_243341,RMVar_hsa_circ_95183,RMVar_hsa_circ_376989,RMVar_hsa_circ_296421,RMVar_hsa_circ_243342,RMVar_hsa_circ_119919,RMVar_hsa_circ_61509,RMVar_hsa_circ_370055,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_372337,RMVar_hsa_circ_243346,RMVar_hsa_circ_341870,RMVar_hsa_circ_243345 114913 RMVar_ID_114913 Human_SNP_ID_867761927 m1A Human chr7 + 128815690 128815690 128815690 AGATGGACTAGCAAAAGAGGAGGAAAAGAAAGAGGAGATGGAGGAGGAAAAAAAGCAAGTGAAAG AGATGGACTAGCAAAAGAGGAGGAAAAGAAAGTGGAGATGGAGGAGGAAAAAAAGCAAGTGAAAG A T CCDC136 Ensembl:ENSG00000128596 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128815650..128815845 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast Human_Splice_Rec_920766,Human_Splice_Rec_920814,Human_Splice_Rec_920840 114914 RMVar_ID_114914 Human_SNP_ID_867762724 m1A Human chr7 - 155739922 155739922 155739922 AGGCCGGAACTGTGGCTGAGACATCGGCATCAAAGGAGGGGGCGGGACGGACAGGTGGTGGTGGT AGGCCGGAACTGTGGCTGAGACATCGGCATCAGAGGAGGGGGCGGGACGGACAGGTGGTGGTGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155739871..155739971 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 114915 RMVar_ID_114915 Human_SNP_ID_867768619 m1A Human chr7 + 112450548 112450548 112450548 GGGGATTTCTGCTGCCGCCACCGCCCACTCTTACCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG GGGGATTTCTGCTGCCGCCACCGCCCACTCTTCCCCCCGCCGCTTCTCGACTCTGTTGTTAGCCG A C IFRD1 Ensembl:ENSG00000006652 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE70485:GSM1972531,GSM1972532 HEK293T,Wild Type;HEPG2 cell line,mRNA heat shock 4h chr7:112450464..112450556;chr7:112450501..112450605 26863410,26863196 MeRIP-seq:(Medium) rs1002929425 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_254084,Human_RBP_ID_673213,Human_RBP_ID_4921450,Human_RBP_ID_5478966,Human_RBP_ID_8655334,Human_RBP_ID_9404849,Human_RBP_ID_18874342,Human_RBP_ID_22463284,Human_RBP_ID_27104078,Human_RBP_ID_27527870 Human_Splice_Rec_911506,Human_Splice_Rec_911508,Human_Splice_Rec_911562 114916 RMVar_ID_114916 Human_SNP_ID_867780313 m1A Human chr7 + 74317598 74317597 74317598 TGAAGCCCCCCGGCCGTGGGGGGAAGCACTCCAGCCCCATGGGCCGGACATCTACTGGGTCAGCT TGAAGCCCCCCGGCCGTGGGGGGAAGCACTCC_GCCCCATGGGCCGGACATCTACTGGGTCAGCT CA C CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:74317580..74317706 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 GBM 1 - Human_Splice_Rec_876369,Human_Splice_Rec_876401 RMVar_hsa_circ_211,RMVar_hsa_circ_245663,RMVar_hsa_circ_92919,RMVar_hsa_circ_245662,RMVar_hsa_circ_288387,RMVar_hsa_circ_298025,RMVar_hsa_circ_333961,RMVar_hsa_circ_107546,RMVar_hsa_circ_245666,RMVar_hsa_circ_245668,RMVar_hsa_circ_245669,RMVar_hsa_circ_245667,RMVar_hsa_circ_245665 114917 RMVar_ID_114917 Human_SNP_ID_867798283 m1A Human chr7 - 7969315 7969315 7969315 GGCTCTGCGGGCCCTGGACGCCGCCGGCCGACACGGAGGCGCGGGGCGGGAGGCGCGCGAGCGTG GGCTCTGCGGGCCCTGGACGCCGCCGGCCGACCCGGAGGCGCGGGGCGGGAGGCGCGCGAGCGTG T G GLCCI1-DT Ensembl:ENSG00000233108 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:7969266..7969379 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 114918 RMVar_ID_114918 Human_SNP_ID_867822662 m1A Human chr7 - 128343781 128343781 128343781 GCTTTGGGTTTCCCGGTCTCATGGCCGGCCTGACCTTATTTGTGGGCCGCCTCCCGCCCTCGGCC GCTTTGGGTTTCCCGGTCTCATGGCCGGCCTGCCCTTATTTGTGGGCCGCCTCCCGCCCTCGGCC T G RBM28 Ensembl:ENSG00000106344 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128343731..128343855 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1681344,Human_RBP_ID_4923648,Human_RBP_ID_8915092,Human_RBP_ID_9311950,Human_RBP_ID_9337359,Human_RBP_ID_9404876,Human_RBP_ID_22111200,Human_RBP_ID_23215639 114919 RMVar_ID_114919 Human_SNP_ID_867827665 m1A Human chr7 - 139045615 139045615 139045615 CCTCTCTCAGGATCTGTATGTAAGTGAAAAGCATCACCATCTACCCATTGGCTCAAGCAGAAATC CCTCTCTCAGGATCTGTATGTAAGTGAAAAGCGTCACCATCTACCCATTGGCTCAAGCAGAAATC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7803490 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1113848,Human_RBP_ID_17314976 GWAS_ID_8753,GWAS_ID_8754,GWAS_ID_8755,GWAS_ID_8756 RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 114920 RMVar_ID_114920 Human_SNP_ID_867828414 m1A Human chr7 + 23507482 23507482 23507482 GTTGGTGTGTGCGCTCTCTTGGTTATAGAATAATCCACCCGAATTCTTCTACCATCCAGCTCCAT GTTGGTGTGTGCGCTCTCTTGGTTATAGAATATTCCACCCGAATTCTTCTACCATCCAGCTCCAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:23507386..23507550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 SKCM,skin desmoplastic 6 skin 114921 RMVar_ID_114921 Human_SNP_ID_867847455 m1A Human chr7 - 26195909 26195909 26195909 AGTAAACGTAATCTTTTTTTGGCCCCTAACAGATGGATATGGCAGTGGACGTGGATTTGGGGATG AGTAAACGTAATCTTTTTTTGGCCCCTAACAGGTGGATATGGCAGTGGACGTGGATTTGGGGATG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:26195797..26195953 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_84112,Human_RBP_ID_681758,Human_RBP_ID_843597,Human_RBP_ID_7727171,Human_RBP_ID_16124473,Human_RBP_ID_22834809,Human_RBP_ID_23080531,Human_RBP_ID_23120483,Human_RBP_ID_24209041,Human_RBP_ID_24389037,Human_RBP_ID_26095543,Human_RBP_ID_26355957,Human_RBP_ID_27829224 Human_Splice_Rec_851104,Human_Splice_Rec_851105,Human_Splice_Rec_851128,Human_Splice_Rec_851129,Human_Splice_Rec_851149,Human_Splice_Rec_851170,Human_Splice_Rec_851171,Human_Splice_Rec_851190,Human_Splice_Rec_851191,Human_Splice_Rec_851208,Human_Splice_Rec_851209,Human_Splice_Rec_851226,Human_Splice_Rec_851227,Human_Splice_Rec_851240 Human_miRNA_ID_2968232,Human_miRNA_ID_2968233 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_61069,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_266045,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_244226,RMVar_hsa_circ_356480,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244227,RMVar_hsa_circ_244228 114922 RMVar_ID_114922 Human_SNP_ID_867875378 m1A Human chr7 + 44767660 44767660 44767660 GTGTTTACCCCAAGCCCGGCGGGGACACGCTCACAGATGTCACCACAGCCCTGCCCTTCATGCCC GTGTTTACCCCAAGCCCGGCGGGGACACGCTCTCAGATGTCACCACAGCCCTGCCCTTCATGCCC A T ZMIZ2 Ensembl:ENSG00000122515 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:44767610..44768000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_5123001,Human_RBP_ID_17427322 Human_miRNA_ID_870377,Human_miRNA_ID_1346223 114923 RMVar_ID_114923 Human_SNP_ID_867891058 m1A Human chr7 - 112206787 112206787 112206787 CACCGTACTCACCCCCATAACCTACACCCCCGACTGTGCTGCAGCTCCCATCACGGTCTTCCTGC CACCGTACTCACCCCCATAACCTACACCCCCGGCTGTGCTGCAGCTCCCATCACGGTCTTCCTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:112206736..112206807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 114924 RMVar_ID_114924 Human_SNP_ID_867913164 m1A Human chr7 - 1547751 1547751 1547751 TCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGAATTCACCAGGTACACCCTGCCTTCCAGCTGGG TCCCCTGCCAGGTGTACGCAGAGAAGAAGGAGTATTCACCAGGTACACCCTGCCTTCCAGCTGGG T A TMEM184A Ensembl:ENSG00000164855 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1546930..1547865 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_Splice_Rec_837783,Human_Splice_Rec_837799,Human_Splice_Rec_837811 114925 RMVar_ID_114925 Human_SNP_ID_867921305 m1A Human chr7 - 25123851 25123851 25123851 GTGTGAAATAACCGATGCATTCTTTCTTGTTTAGGCATCATCTGGGGAGAGGATACACTGATGGA GTGTGAAATAACCGATGCATTCTTTCTTGTTTTGGCATCATCTGGGGAGAGGATACACTGATGGA T A CYCS Ensembl:ENSG00000172115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:25123826..25123941;chr7:25123826..25123940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 15 haematopoietic and lymphoid tissue Human_RBP_ID_7726547 114926 RMVar_ID_114926 Human_SNP_ID_867921314 m1A Human chr7 - 25123851 25123851 25123851 GTGTGAAATAACCGATGCATTCTTTCTTGTTTAGGCATCATCTGGGGAGAGGATACACTGATGGA GTGTGAAATAACCGATGCATTCTTTCTTGTTTGGGCATCATCTGGGGAGAGGATACACTGATGGA T C CYCS Ensembl:ENSG00000172115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:25123826..25123941;chr7:25123826..25123940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 24 haematopoietic and lymphoid tissue Human_RBP_ID_7726547 114927 RMVar_ID_114927 Human_SNP_ID_867921325 m1A Human chr7 - 25123851 25123851 25123851 GTGTGAAATAACCGATGCATTCTTTCTTGTTTAGGCATCATCTGGGGAGAGGATACACTGATGGA GTGTGAAATAACCGATGCATTCTTTCTTGTTTCGGCATCATCTGGGGAGAGGATACACTGATGGA T G CYCS Ensembl:ENSG00000172115 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:25123826..25123941;chr7:25123826..25123940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_7726547 114928 RMVar_ID_114928 Human_SNP_ID_867980434 m1A Human chr7 + 74403952 74403952 74403952 CAGGCAGGAGCCGGGACTGTCACTTTGGAGACAAAACAGTGTTTGTAACAATAACGTACTCACCG CAGGCAGGAGCCGGGACTGTCACTTTGGAGACTAAACAGTGTTTGTAACAATAACGTACTCACCG A T CLIP2 Ensembl:ENSG00000106665 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:74403902..74404202 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_miRNA_ID_2059631,Human_miRNA_ID_2059632,Human_miRNA_ID_2185028,Human_miRNA_ID_2185029,Human_miRNA_ID_2647567,Human_miRNA_ID_2647568,Human_miRNA_ID_2670164,Human_miRNA_ID_2670165,Human_miRNA_ID_3100814,Human_miRNA_ID_3100815 114929 RMVar_ID_114929 Human_SNP_ID_867993198 m1A Human chr7 + 112939659 112939659 112939659 TCTTCACCACACCGGAGAGCTTCTCCTGCTCCAGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG TCTTCACCACACCGGAGAGCTTCTCCTGCTCCGGTTTCCGCTCCTGCTCCCGGGGCGGCGGAGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:112939613..112939773;chr7:112939614..112939758 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 114930 RMVar_ID_114930 Human_SNP_ID_868011755 m1A Human chr7 + 1498512 1498512 1498512 CGCTGGAGAGCTCATTGAAGATCACCAACTTGATGGTGGTGCCCAGGTTGTCCTTGTGCGCGCTC CGCTGGAGAGCTCATTGAAGATCACCAACTTGGTGGTGGTGCCCAGGTTGTCCTTGTGCGCGCTC A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1498461..1498532 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114931 RMVar_ID_114931 Human_SNP_ID_868016649 m1A Human chr7 - 66141534 66141534 66141534 TTTCTCTTCTCCAGAGAGGCTCTGGCACTCTCATGGTGCTGACTTTCATCCTCTGACCCTCCTAC TTTCTCTTCTCCAGAGAGGCTCTGGCACTCTCGTGGTGCTGACTTTCATCCTCTGACCCTCCTAC T C AC068533.3 Ensembl:ENSG00000234185 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66141530..66141618 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114932 RMVar_ID_114932 Human_SNP_ID_868025430 m1A Human chr7 - 834117 834117 834117 AGTCTAAATTCCCAGCCCAGCCTACACCATCCAGCCAGCCCCTGCCCACCAAGAGTCTAAATTCC AGTCTAAATTCCCAGCCCAGCCTACACCATCCGGCCAGCCCCTGCCCACCAAGAGTCTAAATTCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:834004..834375 26863196 MeRIP-seq:(Medium) rs13221885 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114933 RMVar_ID_114933 Human_SNP_ID_868033843 m1A Human chr7 + 100680504 100680488 100680504 TGACCCAGGAGCCGCACACTTCTCTTCACCCCAACCTTACCCAACGGTAAAAAGCGCATCATATC TGACCCAGGAGCCGCAC________________ACCTTACCCAACGGTAAAAAGCGCATCATATC CACTTCTCTTCACCCCA C RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100680351..100680749 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 18..33 33 PAAD 1 - 114934 RMVar_ID_114934 Human_SNP_ID_868034010 m1A Human chr7 - 55964871 55964871 55964871 CCCTCCGTGACCTTGAGCCCGAGGACGCCCCGACCCCGCCCCAGCTCCGGCCCCACCCCAGCTCC CCCTCCGTGACCTTGAGCCCGAGGACGCCCCGCCCCCGCCCCAGCTCCGGCCCCACCCCAGCTCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:55964866..55964990 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 114935 RMVar_ID_114935 Human_SNP_ID_868048623 m1A Human chr7 - 44114865 44114865 44114865 CCACGCAGACCGCCTGCCTTGTGAACCTGCGCAGCCTGGCCTGCCAGCCCATCAGCTTCTCGGGC CCACGCAGACCGCCTGCCTTGTGAACCTGCGCGGCCTGGCCTGCCAGCCCATCAGCTTCTCGGGC T C POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44114814..44114971 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5242986,Human_RBP_ID_17664263,Human_RBP_ID_18195940,Human_RBP_ID_22110747,Human_RBP_ID_22622837,Human_RBP_ID_26830319 Human_Splice_Rec_861742,Human_Splice_Rec_861764,Human_Splice_Rec_861766,Human_Splice_Rec_861784,Human_Splice_Rec_861804 RMVar_hsa_circ_122099,RMVar_hsa_circ_244917 114936 RMVar_ID_114936 Human_SNP_ID_868054558 m1A Human chr7 + 143267714 143267714 143267714 AAAGGTGAAGAACCAGCTCAAGGAGACCACTGAGGCAGCCTGCAGATACGGAGTGAGCAGCTCTT AAAGGTGAAGAACCAGCTCAAGGAGACCACTGGGGCAGCCTGCAGATACGGAGTGAGCAGCTCTT A G GSTK1 Ensembl:ENSG00000197448 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:143267665..143267761 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 4 head and neck Human_RBP_ID_794572,Human_RBP_ID_952858,Human_RBP_ID_5404594,Human_RBP_ID_9404004,Human_RBP_ID_19021551,Human_RBP_ID_23080715,Human_RBP_ID_26356092 Human_Splice_Rec_932698,Human_Splice_Rec_932699,Human_Splice_Rec_932710,Human_Splice_Rec_932711,Human_Splice_Rec_932724,Human_Splice_Rec_932725,Human_Splice_Rec_932738,Human_Splice_Rec_932739,Human_Splice_Rec_932750,Human_Splice_Rec_932751,Human_Splice_Rec_932764,Human_Splice_Rec_932765 RMVar_hsa_circ_2577,RMVar_hsa_circ_279170,RMVar_hsa_circ_249236,RMVar_hsa_circ_342061,RMVar_hsa_circ_310504,RMVar_hsa_circ_365572 114937 RMVar_ID_114937 Human_SNP_ID_868067873 m1A Human chr7 + 39951746 39951746 39951746 CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCCAGCTACAGCCGCCACAGCTCCTACGAGCGGGGC CCCCGAGCCCCTACAGTCGCCGCCGCTCCCCCGGCTACAGCCGCCACAGCTCCTACGAGCGGGGC A G CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:39951604..39951792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung Human_RBP_ID_9337116,Human_RBP_ID_17426934 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 114938 RMVar_ID_114938 Human_SNP_ID_868073165 m1A Human chr7 - 151212645 151212645 151212645 CTCTACAAATAGTAATAAAATGAACCGGGCATAGTAGCATGTGCCTGCGGTCCCAGCTGCTCTGA CTCTACAAATAGTAATAAAATGAACCGGGCATGGTAGCATGTGCCTGCGGTCCCAGCTGCTCTGA T C ABCF2,ABCF2:2 Ensembl:ENSG00000285292,Ensembl:ENSG00000033050 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1065071 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_679015,Human_RBP_ID_1683632,Human_RBP_ID_16068785,Human_RBP_ID_26544977 GWAS_ID_10009,GWAS_ID_10010,GWAS_ID_10011,GWAS_ID_10012,GWAS_ID_10013 RMVar_hsa_circ_117046,RMVar_hsa_circ_249443 114939 RMVar_ID_114939 Human_SNP_ID_868088489 m1A Human chr7 + 73578521 73578521 73578521 GGGCCAGCAGCCCAAGCAACACCGACAGCCCCATGAGCTCCGACATCTGCGAGAGCTCCATGTTG GGGCCAGCAGCCCAAGCAACACCGACAGCCCCGTGAGCTCCGACATCTGCGAGAGCTCCATGTTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:73578308..73578575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114940 RMVar_ID_114940 Human_SNP_ID_868091095 m1A Human chr7 - 149455445 149455445 149455445 GATCACCCGCTTGGCTGTGTGGGCTGCCGTCCAAGCAGTGGAGAGGAAGCTGGAGGCCCAGGCCA GATCACCCGCTTGGCTGTGTGGGCTGCCGTCCTAGCAGTGGAGAGGAAGCTGGAGGCCCAGGCCA T A ZNF777 Ensembl:ENSG00000196453 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:149455395..149455496 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - RMVar_hsa_circ_280120 114941 RMVar_ID_114941 Human_SNP_ID_868093496 m1A Human chr7 - 5603950 5603950 5603950 AGCTGGAGCGGTTGGCGTCCAGGGTGCCCGTGACCTTGCGGCAGCCGATGAAGCCATGCTCCCCG AGCTGGAGCGGTTGGCGTCCAGGGTGCCCGTGCCCTTGCGGCAGCCGATGAAGCCATGCTCCCCG T G RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:5603851..5604063;chr7:5603854..5604045 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 114942 RMVar_ID_114942 Human_SNP_ID_868101030 m1A Human chr7 + 100091827 100091827 100091827 GTACTTGAAGGGCTGATGGACAGGGGTCAGGCAACTATCCCAAAGGGGAGGGCACTACACTTCCT GTACTTGAAGGGCTGATGGACAGGGGTCAGGCGACTATCCCAAAGGGGAGGGCACTACACTTCCT A G COPS6 Ensembl:ENSG00000168090 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100091651..100091954 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_691345,Human_RBP_ID_794469,Human_RBP_ID_1053695,Human_RBP_ID_3120283,Human_RBP_ID_5123046,Human_RBP_ID_5152984,Human_RBP_ID_8675710,Human_RBP_ID_17314358,Human_RBP_ID_17426808,Human_RBP_ID_17543117,Human_RBP_ID_17664286,Human_RBP_ID_18107787,Human_RBP_ID_22464608,Human_RBP_ID_23215573 114943 RMVar_ID_114943 Human_SNP_ID_868116667 m1A Human chr7 + 100098103 100098103 100098103 TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAAAGGGGATGATCCATTCCTCATGTCAAACTCTTC TCTGTGTGGGTAGAATGAGTAGGTGAGGGAAAGGGGGATGATCCATTCCTCATGTCAAACTCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100098102..100098302 26863196 MeRIP-seq:(Medium) rs369912024 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 114944 RMVar_ID_114944 Human_SNP_ID_868169082 m1A Human chr7 - 2115431 2115431 2115431 TGACCCCGGAACACGCGGGGACCCTGTCCAGCACCTCCTCTGACCCCAGAACACGTGGGGACCCT TGACCCCGGAACACGCGGGGACCCTGTCCAGCGCCTCCTCTGACCCCAGAACACGTGGGGACCCT T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:2115404..2115555 26863196 MeRIP-seq:(Medium) rs553908998 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_3862005 RMVar_hsa_circ_5502,RMVar_hsa_circ_35874,RMVar_hsa_circ_339649,RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_24626,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_38270,RMVar_hsa_circ_281224 114945 RMVar_ID_114945 Human_SNP_ID_868185713 m1A Human chr7 + 129880933 129880933 129880933 GTGGTCCATAAAACTTCACTACAAATTCATTAAGTCCTCCCAGGATCGTAACCTCATGTTTACTC GTGGTCCATAAAACTTCACTACAAATTCATTACGTCCTCCCAGGATCGTAACCTCATGTTTACTC A C RF00017-4487,RF00017-1020 RNACentral:URS000095255B,RNACentral:URS000099BA6B SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:129879631..129949000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 114946 RMVar_ID_114946 Human_SNP_ID_868223687 m1A Human chr7 - 127584699 127584699 127584699 GTGGGGAGGTGGACAAAAGACTGCACCAGCTGAAGACTCAGTTGGCTACTTTGACCAGTTCTTTG GTGGGGAGGTGGACAAAAGACTGCACCAGCTGGAGACTCAGTTGGCTACTTTGACCAGTTCTTTG T C GCC1 Ensembl:ENSG00000179562 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:127584649..127584750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 1 oesophagus Human_RBP_ID_8914603,Human_RBP_ID_9311448 Human_miRNA_ID_2667961,Human_miRNA_ID_2947228 RMVar_hsa_circ_80517,RMVar_hsa_circ_248174 114947 RMVar_ID_114947 Human_SNP_ID_868235624 m1A Human chr7 + 22822784 22822784 22822784 GCTTGGCCTCTTTGCTCAGCTTCACCATGGCGACGGCCGTGTGGCGCAGGGAGGACCCCTTACAG GCTTGGCCTCTTTGCTCAGCTTCACCATGGCGTCGGCCGTGTGGCGCAGGGAGGACCCCTTACAG A T NONHSAG047094.2 RNACentral:URS00008BDF34 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:22822624..22822850;chr7:22822701..22822850;chr7:22822614..22822850;chr7:22822608..22822850;chr7:22822626..22822850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary 114948 RMVar_ID_114948 Human_SNP_ID_868251350 m1A Human chr7 + 134941225 134941225 134941225 AGAATTCATGACCCACAAACTTAAACATACTGAGAATACTTTCAGGTAAGAAGTAGCAACTAGTT AGAATTCATGACCCACAAACTTAAACATACTGGGAATACTTTCAGGTAAGAAGTAGCAACTAGTT A G CALD1 Ensembl:ENSG00000122786 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:134941201..134941225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 7 oesophagus Human_RBP_ID_8238142,Human_RBP_ID_8908119,Human_RBP_ID_9403926,Human_RBP_ID_18093067,Human_RBP_ID_19135480,Human_RBP_ID_24549317 Human_Splice_Rec_925409,Human_Splice_Rec_925435,Human_Splice_Rec_925457,Human_Splice_Rec_925497,Human_Splice_Rec_925523,Human_Splice_Rec_925551,Human_Splice_Rec_925571,Human_Splice_Rec_925617,Human_Splice_Rec_925639,Human_Splice_Rec_925663,Human_Splice_Rec_925687,Human_Splice_Rec_925707,Human_Splice_Rec_925709 RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_53510,RMVar_hsa_circ_350384,RMVar_hsa_circ_366213,RMVar_hsa_circ_248678,RMVar_hsa_circ_356673,RMVar_hsa_circ_326037,RMVar_hsa_circ_35162 114949 RMVar_ID_114949 Human_SNP_ID_868261249 m1A Human chr7 + 66995501 66995501 66995501 TCCAGCCTGAAGGCCACCAGCGCCTCGCGGTAACGACCGATCGGCGCGCGGCACTGACCCAACCA TCCAGCCTGAAGGCCACCAGCGCCTCGCGGTAGCGACCGATCGGCGCGCGGCACTGACCCAACCA A G TYW1 Ensembl:ENSG00000198874 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:66995452..66995552 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114950 RMVar_ID_114950 Human_SNP_ID_868262133 m1A Human chr7 + 101154747 101154747 101154747 GGCGCATTTGCAGGGCGAGCGGGGGCTGACGAAGGGGCGGCGGGGCCGTCCCGAGCCGGGAGGGG GGCGCATTTGCAGGGCGAGCGGGGGCTGACGAGGGGGCGGCGGGGCCGTCCCGAGCCGGGAGGGG A G AP1S1 Ensembl:ENSG00000106367 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:101154745..101154831 26863196 MeRIP-seq:(Medium) rs1055747929 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_13942,Human_RBP_ID_8218463,Human_RBP_ID_9439836,Human_RBP_ID_21992530 114951 RMVar_ID_114951 Human_SNP_ID_868262262 m1A Human chr7 - 131654111 131654108 131654111 CACAAATACACACCCCCACAACACATACCACTACAACACATACCACAACACACACACATCACACC CACAAATACACACCCCCACAACACATACCACT___ACACATACCACAACACACACACATCACACC TTGT T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:131653901..131654138 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..35 33 LMS 2 - 114952 RMVar_ID_114952 Human_SNP_ID_868263363 m1A Human chr7 + 263236 263236 263236 CAGCGGGCACAGGACAGAGAAGAGGAAGCCGCAGCAGCCCCAGTGCCGACCAGCAGCGGGCACAG CAGCGGGCACAGGACAGAGAAGAGGAAGCCGCTGCAGCCCCAGTGCCGACCAGCAGCGGGCACAG A T lnc-FAM20C-8 RNACentral:URS00009B9D48 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:263185..263273 26863196 MeRIP-seq:(Medium) rs74190809 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 114953 RMVar_ID_114953 Human_SNP_ID_868266763 m1A Human chr7 + 44568174 44568174 44568174 GGTGGGGCTTCACCACTGCGGGGTGCAAAGGTAGGTCATGCCGCAGCAGCTGGAGGTCCCTAGGG GGTGGGGCTTCACCACTGCGGGGTGCAAAGGTGGGTCATGCCGCAGCAGCTGGAGGTCCCTAGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44568092..44568234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - 114954 RMVar_ID_114954 Human_SNP_ID_868314801 m1A Human chr7 + 157409861 157409861 157409861 CATGCGGAGAGGCCAGAACGCCCTGCCAGCCCAGCCTGCCGGCCTCCGCCCGCCGAAGCCGCCCC CATGCGGAGAGGCCAGAACGCCCTGCCAGCCCTGCCTGCCGGCCTCCGCCCGCCGAAGCCGCCCC A T DNAJB6 Ensembl:ENSG00000105993 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:157409813..157409972;chr7:157409818..157409960 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LIHC 1 - Human_RBP_ID_253131,Human_RBP_ID_792995 Human_Splice_Rec_942942,Human_Splice_Rec_942974,Human_Splice_Rec_942996,Human_Splice_Rec_943054,Human_Splice_Rec_943070 RMVar_hsa_circ_40787,RMVar_hsa_circ_122886,RMVar_hsa_circ_249843 114955 RMVar_ID_114955 Human_SNP_ID_868322084 m1A Human chr7 + 73687015 73687015 73687015 CTTTTCTCTAATGTAGATGAGGCTGTGGACCGAGAGATAGAGGGAGACCTGCTGCTGGGGGATAT CTTTTCTCTAATGTAGATGAGGCTGTGGACCGCGAGATAGAGGGAGACCTGCTGCTGGGGGATAT A C BUD23 Ensembl:ENSG00000071462 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:73687001..73687050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_RBP_ID_956442,Human_RBP_ID_3972009,Human_RBP_ID_9337182,Human_RBP_ID_9354833,Human_RBP_ID_16213626,Human_RBP_ID_19019724,Human_RBP_ID_22464509,Human_RBP_ID_24225633 Human_Splice_Rec_874154,Human_Splice_Rec_874214,Human_Splice_Rec_874215,Human_Splice_Rec_874236,Human_Splice_Rec_874237,Human_Splice_Rec_874248,Human_Splice_Rec_874249,Human_Splice_Rec_874282,Human_Splice_Rec_874283,Human_Splice_Rec_874302,Human_Splice_Rec_874303,Human_Splice_Rec_874324,Human_Splice_Rec_874325,Human_Splice_Rec_874348,Human_Splice_Rec_874349 Human_miRNA_ID_2955509,Human_miRNA_ID_2955510,Human_miRNA_ID_2955511,Human_miRNA_ID_2955512 RMVar_hsa_circ_245593,RMVar_hsa_circ_87453,RMVar_hsa_circ_299918,RMVar_hsa_circ_372258,RMVar_hsa_circ_272645,RMVar_hsa_circ_119564,RMVar_hsa_circ_245595,RMVar_hsa_circ_245596,RMVar_hsa_circ_245594,RMVar_hsa_circ_34847,RMVar_hsa_circ_60048,RMVar_hsa_circ_245592,RMVar_hsa_circ_94878,RMVar_hsa_circ_245598 114956 RMVar_ID_114956 Human_SNP_ID_868331735 m1A Human chr7 - 98317933 98317933 98317933 GTGTGAAATGAGTGAGGGCCCCGGCCAGTGTGAGGATGATGTGAACTGTGGGGTGAGGGTCCCAG GTGTGAAATGAGTGAGGGCCCCGGCCAGTGTGTGGATGATGTGAACTGTGGGGTGAGGGTCCCAG T A BAIAP2L1 Ensembl:ENSG00000006453 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:98317924..98318113 26863196 MeRIP-seq:(Medium) rs1381584434 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_90201,RMVar_hsa_circ_101627,RMVar_hsa_circ_87367,RMVar_hsa_circ_246784,RMVar_hsa_circ_246783,RMVar_hsa_circ_359198,RMVar_hsa_circ_107450,RMVar_hsa_circ_350486,RMVar_hsa_circ_102476,RMVar_hsa_circ_246790,RMVar_hsa_circ_246792,RMVar_hsa_circ_246793,RMVar_hsa_circ_246791,RMVar_hsa_circ_72488,RMVar_hsa_circ_34302,RMVar_hsa_circ_350704,RMVar_hsa_circ_60267,RMVar_hsa_circ_61961,RMVar_hsa_circ_20691 114957 RMVar_ID_114957 Human_SNP_ID_868342211 m1A Human chr7 + 23506260 23506260 23506260 CCTCCACCGCCGCCGCCTCCTCCACCACCCCCACCACTACTGCAGAAAAATGTAAAAATTCTCCA CCTCCACCGCCGCCGCCTCCTCCACCACCCCCCCCACTACTGCAGAAAAATGTAAAAATTCTCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:23506210..23506314 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 114958 RMVar_ID_114958 Human_SNP_ID_868342483 m1A Human chr7 + 128769149 128769149 128769149 AGCCAGGCCACAGATTTTGGGGAGGCCTTAGTACGGCATGATGAGTTCTGAGCTACGGAGGAACC AGCCAGGCCACAGATTTTGGGGAGGCCTTAGTGCGGCATGATGAGTTCTGAGCTACGGAGGAACC A G CALU Ensembl:ENSG00000128595 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:128769051..128769325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_674643,Human_RBP_ID_793411,Human_RBP_ID_843751,Human_RBP_ID_1050295,Human_RBP_ID_4959770,Human_RBP_ID_7691936,Human_RBP_ID_8907502,Human_RBP_ID_9263512,Human_RBP_ID_16003721,Human_RBP_ID_17539349,Human_RBP_ID_18108951,Human_RBP_ID_18875537,Human_RBP_ID_22407073,Human_RBP_ID_22775539,Human_RBP_ID_23072022,Human_RBP_ID_24189071,Human_RBP_ID_27763542 Human_Splice_Rec_920610,Human_Splice_Rec_920624,Human_Splice_Rec_920636,Human_Splice_Rec_920648,Human_Splice_Rec_920662,Human_Splice_Rec_920668,Human_Splice_Rec_920669 RMVar_hsa_circ_248245,RMVar_hsa_circ_81132 114959 RMVar_ID_114959 Human_SNP_ID_868350817 m1A Human chr7 - 22727272 22727272 22727272 GGCTAAGGATTTCCTGCACTTACTTGTGGAGAAGGAGTTCATAGCTGGGCTCCTGGAGGGGAGAT GGCTAAGGATTTCCTGCACTTACTTGTGGAGACGGAGTTCATAGCTGGGCTCCTGGAGGGGAGAT T G STEAP1B,IL6-AS1 Ensembl:ENSG00000105889,Ensembl:ENSG00000179428 Protein coding,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:22727221..22727312 26863196 MeRIP-seq:(Medium) rs958965295 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 8 lung 114960 RMVar_ID_114960 Human_SNP_ID_868367612 m1A Human chr7 - 139045279 139045279 139045279 CACTCTGGCTTCCTTTCAGTTTTGTGGTTCCCATTTTTAGCTAGTTCAGTGGTTTTCAATGGGCA CACTCTGGCTTCCTTTCAGTTTTGTGGTTCCCGTTTTTAGCTAGTTCAGTGGTTTTCAATGGGCA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044551 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17314974,Human_RBP_ID_24439227 GWAS_ID_8738,GWAS_ID_8739,GWAS_ID_8740,GWAS_ID_8741,GWAS_ID_8742,GWAS_ID_8743,GWAS_ID_8744,GWAS_ID_8745,GWAS_ID_8746,GWAS_ID_8747,GWAS_ID_8748,GWAS_ID_8749,GWAS_ID_8750,GWAS_ID_8751,GWAS_ID_8752 RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 114961 RMVar_ID_114961 Human_SNP_ID_868380368 m1A Human chr7 + 2538228 2538228 2538228 TCTAGGGACCTGAGCATGGCCAGCACAGCCTCAGGCTCCTGGTCCCCTGGGGGCTGGGCCTGCTC TCTAGGGACCTGAGCATGGCCAGCACAGCCTCGGGCTCCTGGTCCCCTGGGGGCTGGGCCTGCTC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:2538126..2538300 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 2 kidney 114962 RMVar_ID_114962 Human_SNP_ID_868401590 m1A Human chr7 - 75738600 75738600 75738600 GACCCCAGGGTACCCCAGCTGGCCTGGGGAGAAGGGCAGAGGCGGGCTCGGAGGAGATGGCAGGA GACCCCAGGGTACCCCAGCTGGCCTGGGGAGACGGGCAGAGGCGGGCTCGGAGGAGATGGCAGGA T G HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:75738441..75738683 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_267822,Human_RBP_ID_4955828 Human_miRNA_ID_2937322 114963 RMVar_ID_114963 Human_SNP_ID_868412834 m1A Human chr7 + 44212354 44212354 44212354 ATTCACATCAGAACTGCAGCCCCTGGAAAAGAAGAGACAGCCATAGACGAGGAGCCAGAGTGGGG ATTCACATCAGAACTGCAGCCCCTGGAAAAGATGAGACAGCCATAGACGAGGAGCCAGAGTGGGG A T YKT6 Ensembl:ENSG00000106636 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:44212304..44212543 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_2043162,Human_RBP_ID_7740724,Human_RBP_ID_16160310,Human_RBP_ID_17314549,Human_RBP_ID_17426935 RMVar_hsa_circ_113965,RMVar_hsa_circ_244924,RMVar_hsa_circ_103139,RMVar_hsa_circ_244928 114964 RMVar_ID_114964 Human_SNP_ID_868427512 m1A Human chr7 + 135977180 135977180 135977180 GTGGCAGCAGCAAGCGGATGCCGCCGGGCGAGAGGGAGGCAGGGCCGCGCGAAGCCGGAGAGGAG GTGGCAGCAGCAAGCGGATGCCGCCGGGCGAGTGGGAGGCAGGGCCGCGCGAAGCCGGAGAGGAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:135977131..135977321 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 114965 RMVar_ID_114965 Human_SNP_ID_868432322 m1A Human chr7 + 100107266 100107266 100107266 GCAGGTGGAGCATCACGGAGCAGGCTGAGGGGAGCCGGAGTTGGGCTGGGAGCCATTGGCTTTTG GCAGGTGGAGCATCACGGAGCAGGCTGAGGGGGGCCGGAGTTGGGCTGGGAGCCATTGGCTTTTG A G AP4M1 Ensembl:ENSG00000221838 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100107216..100107331 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas Human_RBP_ID_24234968 114966 RMVar_ID_114966 Human_SNP_ID_868434256 m1A Human chr7 - 127582297 127582297 127582297 GAAGCAGAAGCACAGGCTGGAGGTCGAGGTGCATCAGCTGCAGGATCGGCTGCTGGAGGAGGGCG GAAGCAGAAGCACAGGCTGGAGGTCGAGGTGCGTCAGCTGCAGGATCGGCTGCTGGAGGAGGGCG T C GCC1 Ensembl:ENSG00000179562 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:127582246..127582323 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_RBP_ID_18091467 Human_miRNA_ID_2012370,Human_miRNA_ID_2750503,Human_miRNA_ID_2753467,Human_miRNA_ID_2755401,Human_miRNA_ID_2758744 RMVar_hsa_circ_80517,RMVar_hsa_circ_248174 114967 RMVar_ID_114967 Human_SNP_ID_868436738 m1A Human chr7 + 74376443 74376443 74376443 GCATGACCTGGAGACCGCCATGCACGTGAAGGAGAAGGAGGCCCTGCGAGAGAAGCTGCAGGAGG GCATGACCTGGAGACCGCCATGCACGTGAAGGGGAAGGAGGCCCTGCGAGAGAAGCTGCAGGAGG A G CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:74376362..74376447 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_9403478,Human_RBP_ID_19019736,Human_RBP_ID_24549287 RMVar_hsa_circ_107546,RMVar_hsa_circ_2528,RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_83371,RMVar_hsa_circ_245672,RMVar_hsa_circ_103650,RMVar_hsa_circ_245670,RMVar_hsa_circ_245679,RMVar_hsa_circ_372481,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245685,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_8106,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245693,RMVar_hsa_circ_103611,RMVar_hsa_circ_282092,RMVar_hsa_circ_313787,RMVar_hsa_circ_245694,RMVar_hsa_circ_245692 114968 RMVar_ID_114968 Human_SNP_ID_868443695 m1A Human chr7 + 149266654 149266654 149266654 GGAGTACGGGCTGCTGCAGAGGCGGCTGGAGAATGTGGAGAACTTGCTGCGCAACAGGAACTTCT GGAGTACGGGCTGCTGCAGAGGCGGCTGGAGATTGTGGAGAACTTGCTGCGCAACAGGAACTTCT A T ZNF783 Ensembl:ENSG00000204946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:149266316..149266731 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_9404062 Human_Splice_Rec_935529,Human_Splice_Rec_935553,Human_Splice_Rec_935563 RMVar_hsa_circ_46074,RMVar_hsa_circ_111713,RMVar_hsa_circ_302274,RMVar_hsa_circ_347241,RMVar_hsa_circ_249353,RMVar_hsa_circ_317080,RMVar_hsa_circ_96115,RMVar_hsa_circ_249355,RMVar_hsa_circ_249356,RMVar_hsa_circ_249354 114969 RMVar_ID_114969 Human_SNP_ID_868450240 m1A Human chr7 + 151349132 151349132 151349132 CTAGAATGCTGTGAAAATGAAGTAGAAAAGGTAATAGAAGAAATACGTTGCAAGGCAATTGAGCG CTAGAATGCTGTGAAAATGAAGTAGAAAAGGTTATAGAAGAAATACGTTGCAAGGCAATTGAGCG A T NUB1 Ensembl:ENSG00000013374 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151349010..151349131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_3071566,Human_RBP_ID_18878492,Human_RBP_ID_22319626,Human_RBP_ID_24199948 Human_Splice_Rec_939098,Human_Splice_Rec_939126,Human_Splice_Rec_939154,Human_Splice_Rec_939170,Human_Splice_Rec_939196,Human_Splice_Rec_939208 RMVar_hsa_circ_26889,RMVar_hsa_circ_62488,RMVar_hsa_circ_11909,RMVar_hsa_circ_56150,RMVar_hsa_circ_328647 114970 RMVar_ID_114970 Human_SNP_ID_868473547 m1A Human chr7 + 2379195 2379195 2379195 GGAAGATTTCCGGAAGTACCGGAAAATGGCCCAGGAGCTCTATATGGAGCAGAAAAACGAGCGCC GGAAGATTTCCGGAAGTACCGGAAAATGGCCCGGGAGCTCTATATGGAGCAGAAAAACGAGCGCC A G EIF3B Ensembl:ENSG00000106263 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:2379146..2379276 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_681412,Human_RBP_ID_953523,Human_RBP_ID_1051530,Human_RBP_ID_1685168,Human_RBP_ID_2040167,Human_RBP_ID_3970753,Human_RBP_ID_7725686,Human_RBP_ID_8910319,Human_RBP_ID_9263409,Human_RBP_ID_16119567 Human_Splice_Rec_838416,Human_Splice_Rec_838417,Human_Splice_Rec_838462,Human_Splice_Rec_838463,Human_Splice_Rec_838491,Human_Splice_Rec_838498,Human_Splice_Rec_838499,Human_Splice_Rec_838503,Human_Splice_Rec_838506,Human_Splice_Rec_838507 Human_miRNA_ID_2039387,Human_miRNA_ID_3018367 RMVar_hsa_circ_9806,RMVar_hsa_circ_66703,RMVar_hsa_circ_126752,RMVar_hsa_circ_243335,RMVar_hsa_circ_56018,RMVar_hsa_circ_119919,RMVar_hsa_circ_79550,RMVar_hsa_circ_87101,RMVar_hsa_circ_113938,RMVar_hsa_circ_243343,RMVar_hsa_circ_243344,RMVar_hsa_circ_243347,RMVar_hsa_circ_127916,RMVar_hsa_circ_338838,RMVar_hsa_circ_243350,RMVar_hsa_circ_243351,RMVar_hsa_circ_78213,RMVar_hsa_circ_243352,RMVar_hsa_circ_243354,RMVar_hsa_circ_76571,RMVar_hsa_circ_243353 114971 RMVar_ID_114971 Human_SNP_ID_868507885 m1A Human chr7 - 88218941 88218941 88218941 GAATGACGTGTATGTGTTTCCTGTTTCACAGTATGGAGGGGCTCCCGGAGGGCCTGCGTTTCCCG GAATGACGTGTATGTGTTTCCTGTTTCACAGTGTGGAGGGGCTCCCGGAGGGCCTGCGTTTCCCG T C SRI Ensembl:ENSG00000075142 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:88218851..88220050 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 5 stomach Human_RBP_ID_4956461,Human_RBP_ID_8944175,Human_RBP_ID_9337217,Human_RBP_ID_22464555 Human_Splice_Rec_886042,Human_Splice_Rec_886043,Human_Splice_Rec_886056,Human_Splice_Rec_886057,Human_Splice_Rec_886083,Human_Splice_Rec_886095,Human_Splice_Rec_886106,Human_Splice_Rec_886107,Human_Splice_Rec_886120,Human_Splice_Rec_886121,Human_Splice_Rec_886130,Human_Splice_Rec_886131,Human_Splice_Rec_886135 RMVar_hsa_circ_21179,RMVar_hsa_circ_334501 114972 RMVar_ID_114972 Human_SNP_ID_868522004 m1A Human chr7 + 27174083 27174083 27174083 CGCCCAGCGTGGGGAAGAGCCCGCAGCTCTGCAGCCCGTAGGGCAGGTCGGCGGCGGGCGGCAGG CGCCCAGCGTGGGGAAGAGCCCGCAGCTCTGCGGCCCGTAGGGCAGGTCGGCGGCGGGCGGCAGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:27173982..27174131 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 114973 RMVar_ID_114973 Human_SNP_ID_868534350 m1A Human chr7 - 5606179 5606179 5606179 GCTTCCAGTCAGGCTAGGGTGAAAGGAAAGAGACAGGAGGAAGACGGCCCCCACACCCCTACCCG GCTTCCAGTCAGGCTAGGGTGAAAGGAAAGAGGCAGGAGGAAGACGGCCCCCACACCCCTACCCG T C RF00017-4552 RNACentral:URS0000973F83 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:5605829..5606222 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 114974 RMVar_ID_114974 Human_SNP_ID_868539276 m1A Human chr7 - 151134437 151134436 151134437 GCTTCCCTGGCACTTTCACCGTTGTCCGCAGCAGGTCAATCTCCTTGCCGTGGATGTTCTGCATG GCTTCCCTGGCACTTTCACCGTTGTCCGCAGC_GGTCAATCTCCTTGCCGTGGATGTTCTGCATG CT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:151134423..151136281 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 SKCM 1 - 114975 RMVar_ID_114975 Human_SNP_ID_868595721 m1A Human chr7 - 26195893 26195893 26195893 TTTTGGCCCCTAACAGATGGATATGGCAGTGGACGTGGATTTGGGGATGGCTATAATGGGTATGG TTTTGGCCCCTAACAGATGGATATGGCAGTGGGCGTGGATTTGGGGATGGCTATAATGGGTATGG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:26195815..26195950 26863410 MeRIP-seq:(Medium) rs199650578 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_84112,Human_RBP_ID_253295,Human_RBP_ID_681757,Human_RBP_ID_843597,Human_RBP_ID_1051625,Human_RBP_ID_1220971,Human_RBP_ID_1685439,Human_RBP_ID_2040485,Human_RBP_ID_3124440,Human_RBP_ID_3842098,Human_RBP_ID_5219346,Human_RBP_ID_5622856,Human_RBP_ID_7727169,Human_RBP_ID_8665211,Human_RBP_ID_8910397,Human_RBP_ID_16124473,Human_RBP_ID_18098039,Human_RBP_ID_18451529,Human_RBP_ID_18880879,Human_RBP_ID_22515637,Human_RBP_ID_23080531,Human_RBP_ID_23120483,Human_RBP_ID_23139986,Human_RBP_ID_24209041,Human_RBP_ID_24389037,Human_RBP_ID_26131031,Human_RBP_ID_26355956,Human_RBP_ID_27829224 Human_Splice_Rec_851104,Human_Splice_Rec_851105,Human_Splice_Rec_851128,Human_Splice_Rec_851129,Human_Splice_Rec_851149,Human_Splice_Rec_851170,Human_Splice_Rec_851171,Human_Splice_Rec_851190,Human_Splice_Rec_851191,Human_Splice_Rec_851208,Human_Splice_Rec_851209,Human_Splice_Rec_851226,Human_Splice_Rec_851227,Human_Splice_Rec_851240 Human_miRNA_ID_2968232,Human_miRNA_ID_2968233 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_61069,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_266045,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_244226,RMVar_hsa_circ_356480,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244227,RMVar_hsa_circ_244228 114976 RMVar_ID_114976 Human_SNP_ID_868600806 m1A Human chr7 - 100887481 100887481 100887481 CTTGAATTTCTTGCCACTGAGAGGACACAGCCACTTATCCTTGCCCAGTTCCTGCGTGTTGGAGG CTTGAATTTCTTGCCACTGAGAGGACACAGCCCCTTATCCTTGCCCAGTTCCTGCGTGTTGGAGG T G RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100887326..100887480 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 114977 RMVar_ID_114977 Human_SNP_ID_868611192 m1A Human chr7 + 143381668 143381668 143381668 CGCAGAAGAAGTTCGGCCCTGTGGTGGCCCCAAAGCCCAAAGTGAATCCCTTCCGGCCCGGGGAC CGCAGAAGAAGTTCGGCCCTGTGGTGGCCCCAGAGCCCAAAGTGAATCCCTTCCGGCCCGGGGAC A G ZYX Ensembl:ENSG00000159840 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:143381301..143381837 26863196 MeRIP-seq:(Medium) rs910264793 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4956737,Human_RBP_ID_9337424 RMVar_hsa_circ_2163,RMVar_hsa_circ_9427 114978 RMVar_ID_114978 Human_SNP_ID_868652498 m1A Human chr7 + 5359494 5359494 5359494 CCCATTCCGATGAGGGCATCATGTTCCTCCTCAGACCCCTTGTGTCTCTTTCTTATCCCTGCTCC CCCATTCCGATGAGGGCATCATGTTCCTCCTCCGACCCCTTGTGTCTCTTTCTTATCCCTGCTCC A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:5359446..5359593 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 114979 RMVar_ID_114979 Human_SNP_ID_868657334 m1A Human chr7 + 56291386 56291386 56291386 CAAGCGCTTCAGCAGCCTGATGCTAAAGTTTTAAAAAATTACTTAAAGGTGTTCTTCCAGAGAGC CAAGCGCTTCAGCAGCCTGATGCTAAAGTTTTTAAAAATTACTTAAAGGTGTTCTTCCAGAGAGC A T AC073136.1 Ensembl:ENSG00000223559 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879186527 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_7779009,Human_RBP_ID_17587020 114980 RMVar_ID_114980 Human_SNP_ID_868660775 m1A Human chr7 - 152135512 152135511 152135513 AACACAAAAATTTGAAAAAGTTAAAAAAAAAAAGGAGATGTGATTATGCTTACAGCTGCAGGACT AACACAAAAATTTGAAAAAGTTAAAAAAAAA__GGAGATGTGATTATGCTTACAGCTGCAGGACT CTT C KMT2C Ensembl:ENSG00000055609 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 32..33 33 UCEC 4 - Human_RBP_ID_679304,Human_RBP_ID_24200540 Human_miRNA_ID_219166,Human_miRNA_ID_674820 RMVar_hsa_circ_249485,RMVar_hsa_circ_115161,RMVar_hsa_circ_93711,RMVar_hsa_circ_249484 114981 RMVar_ID_114981 Human_SNP_ID_868661007 m1A Human chr7 - 23319219 23319219 23319219 TCAGAAACGGAGACTGTTCATCTGTTTATCCCAGCTCTATCAGTCGGTGCCATCATCGGCAAGCA TCAGAAACGGAGACTGTTCATCTGTTTATCCCTGCTCTATCAGTCGGTGCCATCATCGGCAAGCA T A IGF2BP3 Ensembl:ENSG00000136231 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:23319181..23342140 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_681248,Human_RBP_ID_9403200,Human_RBP_ID_17312492,Human_RBP_ID_17540747,Human_RBP_ID_22774297 Human_Splice_Rec_849572,Human_Splice_Rec_849573,Human_Splice_Rec_849582,Human_Splice_Rec_849583,Human_Splice_Rec_849612,Human_Splice_Rec_849613,Human_Splice_Rec_849622 Human_miRNA_ID_2133842 RMVar_hsa_circ_4059,RMVar_hsa_circ_91995,RMVar_hsa_circ_113735,RMVar_hsa_circ_108136,RMVar_hsa_circ_95258,RMVar_hsa_circ_244099,RMVar_hsa_circ_244100,RMVar_hsa_circ_244097,RMVar_hsa_circ_244098,RMVar_hsa_circ_86273,RMVar_hsa_circ_121688,RMVar_hsa_circ_103102,RMVar_hsa_circ_244106,RMVar_hsa_circ_113358,RMVar_hsa_circ_244104,RMVar_hsa_circ_102358,RMVar_hsa_circ_290108,RMVar_hsa_circ_244105,RMVar_hsa_circ_317577,RMVar_hsa_circ_276147,RMVar_hsa_circ_244108,RMVar_hsa_circ_244110,RMVar_hsa_circ_52764,RMVar_hsa_circ_244109,RMVar_hsa_circ_244107,RMVar_hsa_circ_244111,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112 114982 RMVar_ID_114982 Human_SNP_ID_868675323 m1A Human chr7 - 56068573 56068573 56068573 ATGGCAAAGGGTTTCACTGTCGCCTCCCGCACAGGCCCGTCACCATCTCTGCTGTCTGGAGAATT ATGGCAAAGGGTTTCACTGTCGCCTCCCGCACTGGCCCGTCACCATCTCTGCTGTCTGGAGAATT T A - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA heat shock 4h chr7:56068391..56068619;chr7:56068419..56068650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 7 lung 114983 RMVar_ID_114983 Human_SNP_ID_868679287 m1A Human chr7 - 96709807 96709807 96709807 GTGGCGTTTCCTTGAGGAAGAGTGAGGGTTCCAACTTTTCTGCTTATCTGGGAGGTGTTGGGCGC GTGGCGTTTCCTTGAGGAAGAGTGAGGGTTCCCACTTTTCTGCTTATCTGGGAGGTGTTGGGCGC T G SEM1 Ensembl:ENSG00000127922 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:96709648..96709875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_84272,Human_RBP_ID_3858824,Human_RBP_ID_4952628,Human_RBP_ID_8674739,Human_RBP_ID_9215444,Human_RBP_ID_24233084 RMVar_hsa_circ_97745,RMVar_hsa_circ_246734 114984 RMVar_ID_114984 Human_SNP_ID_868699805 m1A Human chr7 - 128531752 128531752 128531752 TCCACGCTCCTCCCGGGAGGGGCCCCGACCCGACCCGGCTGCGGGCCGCTCCGCTCTCCCCCTGG TCCACGCTCCTCCCGGGAGGGGCCCCGACCCGCCCCGGCTGCGGGCCGCTCCGCTCTCCCCCTGG T G RF00017-4674 RNACentral:URS000094E2D9 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128531702..128531901 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114985 RMVar_ID_114985 Human_SNP_ID_868729655 m1A Human chr7 - 73840111 73840111 73840111 CACCCCCCCCCACACACACACAGGGACCTTCGACGCGGTGCTGATAGTCGGTGCCCTCAGTGACG CACCCCCCCCCACACACACACAGGGACCTTCGGCGCGGTGCTGATAGTCGGTGCCCTCAGTGACG T C METTL27 Ensembl:ENSG00000165171 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:73840019..73840460 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney Human_Splice_Rec_874640,Human_Splice_Rec_874641,Human_Splice_Rec_874648,Human_Splice_Rec_874649,Human_Splice_Rec_874656 114986 RMVar_ID_114986 Human_SNP_ID_868740638 m1A Human chr7 - 2092409 2092409 2092409 CGTGAGGGAGGATGCTTGGGTGGGGCGTGGTCATGCACACCTGTGATCCTAGCATTTTAGGAGGC CGTGAGGGAGGATGCTTGGGTGGGGCGTGGTCGTGCACACCTGTGATCCTAGCATTTTAGGAGGC T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2092406..2092641 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_5502,RMVar_hsa_circ_35874,RMVar_hsa_circ_339649,RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_104757,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243304,RMVar_hsa_circ_107446,RMVar_hsa_circ_243306,RMVar_hsa_circ_24626,RMVar_hsa_circ_243305,RMVar_hsa_circ_31714,RMVar_hsa_circ_38270,RMVar_hsa_circ_281224 114987 RMVar_ID_114987 Human_SNP_ID_868772834 m1A Human chr7 - 100577391 100577391 100577391 GGTCTGCCCCTCTTGCCCTGTCTTGGTCCCTCAGGCGGGAGGAGCCGGCAGGGGAGGAGCGGCGG GGTCTGCCCCTCTTGCCCTGTCTTGGTCCCTCGGGCGGGAGGAGCCGGCAGGGGAGGAGCGGCGG T C AC069281.2,LRCH4 Ensembl:ENSG00000274272,Ensembl:ENSG00000077454 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100577366..100577514 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_253998,Human_RBP_ID_954723,Human_RBP_ID_5090582,Human_RBP_ID_5220066,Human_RBP_ID_23215581,Human_RBP_ID_26132122 114988 RMVar_ID_114988 Human_SNP_ID_868785281 m1A Human chr7 + 66087351 66087351 66087351 TCCCTGTCCCTGCAGTGGGGCCATTGCAGGCAATCCCCTGGGTGTGGACCGAGAGCTGCTCCGAG TCCCTGTCCCTGCAGTGGGGCCATTGCAGGCAGTCCCCTGGGTGTGGACCGAGAGCTGCTCCGAG A G ASL Ensembl:ENSG00000126522 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:66087346..66088868 32194978 MeRIP-seq:(Medium) rs763948849 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas Human_RBP_ID_954470,Human_RBP_ID_5403060,Human_RBP_ID_24221603,Human_RBP_ID_26356485 Human_Splice_Rec_870682,Human_Splice_Rec_870683,Human_Splice_Rec_870710,Human_Splice_Rec_870711,Human_Splice_Rec_870798,Human_Splice_Rec_870799,Human_Splice_Rec_870826,Human_Splice_Rec_870827,Human_Splice_Rec_870876,Human_Splice_Rec_870877,Human_Splice_Rec_870904,Human_Splice_Rec_870905,Human_Splice_Rec_870928,Human_Splice_Rec_870929,Human_Splice_Rec_870950,Human_Splice_Rec_870960,Human_Splice_Rec_870961 RMVar_hsa_circ_33843,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245323,RMVar_hsa_circ_118242,RMVar_hsa_circ_61514,RMVar_hsa_circ_350597,RMVar_hsa_circ_360166,RMVar_hsa_circ_342396,RMVar_hsa_circ_120280,RMVar_hsa_circ_245324 114989 RMVar_ID_114989 Human_SNP_ID_868790637 m1A Human chr7 + 10940093 10940093 10940093 TGCGGCAGAGGTCTCCGACTGGAAAGGAGAGAACCGACCTAGCCACCAGGCCCTAAGCTAAAAAT TGCGGCAGAGGTCTCCGACTGGAAAGGAGAGAGCCGACCTAGCCACCAGGCCCTAAGCTAAAAAT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:10939975..10940175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 114990 RMVar_ID_114990 Human_SNP_ID_868797095 m1A Human chr7 + 1555447 1555447 1555447 TGGGCTGCGGCCAGTTCGCTGACACCAGGGGGACGCCGGCTGTCTCCAGGATCCCTGAGACATTA TGGGCTGCGGCCAGTTCGCTGACACCAGGGGGGCGCCGGCTGTCTCCAGGATCCCTGAGACATTA A G L13304-001,L13705-009,lnc-ELFN1-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00009AFF67 scRNA,misc_RNA,lincRNA intron,intron,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:1555414..1555493 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system tuberous_sclerosis_tuber,cerebral_cortex tuberous_sclerosis_tuber 1 brain 114991 RMVar_ID_114991 Human_SNP_ID_868879793 m1A Human chr7 - 100870640 100870640 100870640 ATGTAGAACATACAAAGCAGCCCACGTGAAAGACGCGATCAAGGGCCACAACCCCAGCCCCATCC ATGTAGAACATACAAAGCAGCCCACGTGAAAGGCGCGATCAAGGGCCACAACCCCAGCCCCATCC T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100870488..100870837 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 114992 RMVar_ID_114992 Human_SNP_ID_868892423 m1A Human chr7 - 44761495 44761495 44761495 TGCTGCAGGCGGAAGGGCTCCAGGACCACCCCATCGCGCACAGGGAAGGTCAGCCGCAACTCGTC TGCTGCAGGCGGAAGGGCTCCAGGACCACCCCGTCGCGCACAGGGAAGGTCAGCCGCAACTCGTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44760590..44763376 32194978 MeRIP-seq:(Medium) rs1329405799 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 8 head and neck 114993 RMVar_ID_114993 Human_SNP_ID_868893066 m1A Human chr7 + 158878466 158878466 158878466 GGGCGCCATGTGGGGTGGCCAGGAGGGCCGACAGTGAGTGCCGGGTGCCATGTGGAGGGGCCAGG GGGCGCCATGTGGGGTGGCCAGGAGGGCCGACTGTGAGTGCCGGGTGCCATGTGGAGGGGCCAGG A T WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:158878461..158878532 26863196 MeRIP-seq:(Medium) rs1333142927 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_24204896 RMVar_hsa_circ_1244,RMVar_hsa_circ_69985,RMVar_hsa_circ_325007,RMVar_hsa_circ_303490,RMVar_hsa_circ_308751,RMVar_hsa_circ_58027,RMVar_hsa_circ_60480,RMVar_hsa_circ_51711,RMVar_hsa_circ_18294,RMVar_hsa_circ_324452,RMVar_hsa_circ_351150,RMVar_hsa_circ_63693,RMVar_hsa_circ_249933 114994 RMVar_ID_114994 Human_SNP_ID_868902911 m1A Human chr7 - 44884611 44884611 44884611 GTGGGCTGCAACAAATACGGGGTGTTTCTGCGAGTGAGCGAGGTGAAGCCGTCCTACCGCAATGC GTGGGCTGCAACAAATACGGGGTGTTTCTGCGTGTGAGCGAGGTGAAGCCGTCCTACCGCAATGC T A PURB Ensembl:ENSG00000146676 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:44884563..44884863 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 1 head and neck Human_RBP_ID_1052322,Human_RBP_ID_1687324,Human_RBP_ID_2043706,Human_RBP_ID_7743001,Human_RBP_ID_8911414,Human_RBP_ID_17541586,Human_RBP_ID_22110766,Human_RBP_ID_24217074 114995 RMVar_ID_114995 Human_SNP_ID_868909596 m1A Human chr7 - 76549387 76549387 76549387 AGACTCGGTGATTCTCGTCCACTAGAGGCCAAAGCCTGGGAACCAGAGCAAGCGATGACCTGAAC AGACTCGGTGATTCTCGTCCACTAGAGGCCAACGCCTGGGAACCAGAGCAAGCGATGACCTGAAC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76549342..76549663 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 114996 RMVar_ID_114996 Human_SNP_ID_868911172 m1A Human chr7 - 155298222 155298222 155298222 AAGAAGGGGGTCATCAAGTTCACTCAGAAGAGACAAAGAGCGAGGAAGGCCCCGCGGGACGCGAA AAGAAGGGGGTCATCAAGTTCACTCAGAAGAGCCAAAGAGCGAGGAAGGCCCCGCGGGACGCGAA T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:155298219..155298525 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 114997 RMVar_ID_114997 Human_SNP_ID_868921597 m1A Human chr7 + 149874076 149874076 149874076 CCTGGGCATCCTGCGCCCGGCCATGACGGCGCACTCATTCGCCCTCCCGGTCATCATCTTCACCA CCTGGGCATCCTGCGCCCGGCCATGACGGCGCGCTCATTCGCCCTCCCGGTCATCATCTTCACCA A G ATP6V0E2 Ensembl:ENSG00000171130 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:149873976..149874820 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 10 liver Human_RBP_ID_4930395,Human_RBP_ID_5479217,Human_RBP_ID_5512836,Human_RBP_ID_8661766,Human_RBP_ID_9405009,Human_RBP_ID_27107640,Human_RBP_ID_27353550 Human_Splice_Rec_936295,Human_Splice_Rec_936299,Human_Splice_Rec_936303,Human_Splice_Rec_936309,Human_Splice_Rec_936315,Human_Splice_Rec_936323,Human_Splice_Rec_936331,Human_Splice_Rec_936337,Human_Splice_Rec_936341,Human_Splice_Rec_936349,Human_Splice_Rec_936353 114998 RMVar_ID_114998 Human_SNP_ID_868922054 m1A Human chr7 + 30504618 30504618 30504618 AGAAGAACGCCGCCGAGGGGTTTCGGAGGTGGATCCTCTCTGTCAGCAGGTTGCTGCCGTAGGCA AGAAGAACGCCGCCGAGGGGTTTCGGAGGTGGCTCCTCTCTGTCAGCAGGTTGCTGCCGTAGGCA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:30498937..30524416 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 114999 RMVar_ID_114999 Human_SNP_ID_868923521 m1A Human chr7 - 157240648 157240648 157240648 ATTTCCTCTCTAAACAGCCTAGATTCAAAGGCAGGCTCTTGTAACCACTCTGAACTTGCAACCAA ATTTCCTCTCTAAACAGCCTAGATTCAAAGGCTGGCTCTTGTAACCACTCTGAACTTGCAACCAA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:157240638..157240789 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115000 RMVar_ID_115000 Human_SNP_ID_868951260 m1A Human chr7 - 26193677 26193677 26193677 CTTATTTTATAATAGGTGGCAATTTTGGAGGTAGCCCCGGTTATGGAGGAGGAAGAGGAGGATAT CTTATTTTATAATAGGTGGCAATTTTGGAGGTTGCCCCGGTTATGGAGGAGGAAGAGGAGGATAT T A HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:26193571..26193742 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_14354,Human_RBP_ID_84110,Human_RBP_ID_253292,Human_RBP_ID_681748,Human_RBP_ID_793272,Human_RBP_ID_844467,Human_RBP_ID_1051621,Human_RBP_ID_1070150,Human_RBP_ID_1143752,Human_RBP_ID_1220962,Human_RBP_ID_2040464,Human_RBP_ID_3082730,Human_RBP_ID_3842083,Human_RBP_ID_4936416,Human_RBP_ID_7727115,Human_RBP_ID_8910395,Human_RBP_ID_9209573,Human_RBP_ID_9403225,Human_RBP_ID_16124336,Human_RBP_ID_17425119,Human_RBP_ID_18098035,Human_RBP_ID_18451528,Human_RBP_ID_19020635,Human_RBP_ID_22463912,Human_RBP_ID_23080628,Human_RBP_ID_23120481,Human_RBP_ID_23139985,Human_RBP_ID_24549102,Human_RBP_ID_26356336,Human_RBP_ID_26724167,Human_RBP_ID_27111213,Human_RBP_ID_27767188,Human_RBP_ID_27829222,Human_RBP_ID_27842871 Human_Splice_Rec_851106,Human_Splice_Rec_851130,Human_Splice_Rec_851150,Human_Splice_Rec_851172,Human_Splice_Rec_851192,Human_Splice_Rec_851210,Human_Splice_Rec_851228 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_68397,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_244220,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_244226 115001 RMVar_ID_115001 Human_SNP_ID_868952473 m1A Human chr7 + 152872826 152872826 152872826 GAGGGTCGGTCCGGTGGCCATGCAGGAGGGGCAGTCCGGTGGCTGGGCAGGAGGGGTGGTCCGGT GAGGGTCGGTCCGGTGGCCATGCAGGAGGGGCGGTCCGGTGGCTGGGCAGGAGGGGTGGTCCGGT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:152872778..152872869 26863196 MeRIP-seq:(Medium) rs911580963 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115002 RMVar_ID_115002 Human_SNP_ID_868956376 m1A Human chr7 - 2594824 2594824 2594824 CTCACCTGTCACTATGTGATGAAGGCCGGCACAGGGCAGGGTGGGGCGGGCGGTCCAGGCGGAGA CTCACCTGTCACTATGTGATGAAGGCCGGCACGGGGCAGGGTGGGGCGGGCGGTCCAGGCGGAGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:2594823..2594913 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 8 large intestine 115003 RMVar_ID_115003 Human_SNP_ID_868990661 m1A Human chr7 + 65982171 65982171 65982171 CAACGGCCCGAGCGCCGCCCAGGCAACCGCCGACCCCCGGGCCATGCTTCCCGGTCCCCCGCTCG CAACGGCCCGAGCGCCGCCCAGGCAACCGCCGGCCCCCGGGCCATGCTTCCCGGTCCCCCGCTCG A G lnc-VKORC1L1-2,RF00017-4520,RF00017-4552 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:65981939..65982225 26863196 MeRIP-seq:(Medium) rs190496263 Functional Loss SNV COSMIC 33..33 33 skin basal_cell_carcinoma,face basal_cell_carcinoma 2 skin,head and neck Clinvar_Rec_490 RMVar_hsa_circ_118631,RMVar_hsa_circ_245295 115004 RMVar_ID_115004 Human_SNP_ID_869023172 m1A Human chr7 - 150323513 150323513 150323513 GGCAGCCTGCGGAGCCACTGGCCAAGCTGGGAAGTCCGGCGCAACTCCGCACCGCAGAGCCGGCG GGCAGCCTGCGGAGCCACTGGCCAAGCTGGGATGTCCGGCGCAACTCCGCACCGCAGAGCCGGCG T A ACTR3C Ensembl:ENSG00000106526 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:150323244..150323575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 MESO 1 - Human_RBP_ID_4956771 Human_Splice_Rec_936585,Human_Splice_Rec_936615 115005 RMVar_ID_115005 Human_SNP_ID_869033987 m1A Human chr7 + 75983630 75983630 75983630 CATGCACCTGGAATTGGACATCTCGGACTCCAAAATCAGGTACCAGCTGCCACTGTCACCCCCTG CATGCACCTGGAATTGGACATCTCGGACTCCACAATCAGGTACCAGCTGCCACTGTCACCCCCTG A C POR Ensembl:ENSG00000127948 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:75983531..75983681 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3972069 Human_Splice_Rec_878785,Human_Splice_Rec_878823,Human_Splice_Rec_878879,Human_Splice_Rec_878897,Human_Splice_Rec_878923,Human_Splice_Rec_878961,Human_Splice_Rec_878967,Human_Splice_Rec_878981 RMVar_hsa_circ_103197,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762,RMVar_hsa_circ_75971,RMVar_hsa_circ_86094,RMVar_hsa_circ_321164,RMVar_hsa_circ_245767,RMVar_hsa_circ_245768,RMVar_hsa_circ_245766 115006 RMVar_ID_115006 Human_SNP_ID_869038366 m1A Human chr7 + 5529583 5529583 5529583 CCCACGATGGAGGGGAAGACGGCCCGGGGGGCATCGTCGCCCGCGAAGCCGGCCTTGCACATGCC CCCACGATGGAGGGGAAGACGGCCCGGGGGGCTTCGTCGCCCGCGAAGCCGGCCTTGCACATGCC A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:5529380..5529727 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115007 RMVar_ID_115007 Human_SNP_ID_869053958 m1A Human chr7 + 23531856 23531856 23531856 TGTCGACGAGGCGCTCCCCAGAACTAAATAAGAGACAAGTCTCGGCTCGAGGGCCGATGGCCTAA TGTCGACGAGGCGCTCCCCAGAACTAAATAAGCGACAAGTCTCGGCTCGAGGGCCGATGGCCTAA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:23531826..23531975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 115008 RMVar_ID_115008 Human_SNP_ID_869055478 m1A Human chr7 + 5431580 5431579 5431581 TCACACACAGACACACACACACACACACACACAGAGTCACCTCCCCCCACCTTTTTTTCCTTTTT TCACACACAGACACACACACACACACACACAC__AGTCACCTCCCCCCACCTTTTTTTCCTTTTT CAG C RF00017-4486,RF00017-4498 RNACentral:URS000090F764,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:5431576..5431703 26863196 MeRIP-seq:(Medium) rs764386496 Functional Loss DEL ICGC 33..34 33 PBCA 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115009 RMVar_ID_115009 Human_SNP_ID_869055632 m1A Human chr7 + 155711371 155711371 155711371 CTCCCCAGCTAGAGACCCCAAGGATGATGATGACCCCGCCACCCGTGACTCCACAGCAGCCCAAG CTCCCCAGCTAGAGACCCCAAGGATGATGATGCCCCCGCCACCCGTGACTCCACAGCAGCCCAAG A C RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:155711249..155711482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_9405051,Human_RBP_ID_16083032,Human_RBP_ID_18878996,Human_RBP_ID_26357404,Human_RBP_ID_27830066 Human_Splice_Rec_942029,Human_Splice_Rec_942073,Human_Splice_Rec_942089,Human_Splice_Rec_942097,Human_Splice_Rec_942115 Human_miRNA_ID_2146491,Human_miRNA_ID_2987916,Human_miRNA_ID_3021614 RMVar_hsa_circ_72846,RMVar_hsa_circ_43949,RMVar_hsa_circ_306816,RMVar_hsa_circ_114504,RMVar_hsa_circ_124662,RMVar_hsa_circ_249670,RMVar_hsa_circ_120729,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_249680,RMVar_hsa_circ_369595,RMVar_hsa_circ_127344,RMVar_hsa_circ_249687,RMVar_hsa_circ_249685,RMVar_hsa_circ_339501,RMVar_hsa_circ_336683,RMVar_hsa_circ_249693,RMVar_hsa_circ_358134,RMVar_hsa_circ_363833,RMVar_hsa_circ_334601,RMVar_hsa_circ_61000,RMVar_hsa_circ_42301,RMVar_hsa_circ_285535,RMVar_hsa_circ_72053,RMVar_hsa_circ_110596,RMVar_hsa_circ_125145,RMVar_hsa_circ_73384,RMVar_hsa_circ_249695,RMVar_hsa_circ_126622,RMVar_hsa_circ_368148,RMVar_hsa_circ_112913,RMVar_hsa_circ_80095,RMVar_hsa_circ_82952,RMVar_hsa_circ_77184,RMVar_hsa_circ_249696,RMVar_hsa_circ_249698,RMVar_hsa_circ_249700,RMVar_hsa_circ_249701,RMVar_hsa_circ_249702,RMVar_hsa_circ_249699,RMVar_hsa_circ_249697 115010 RMVar_ID_115010 Human_SNP_ID_869063584 m1A Human chr7 - 56060858 56060858 56060858 CCCTGCCCTTTACACTGGGCTTATGTTTAATCAGGGCTTCTGCCATTGCCACTTCCACGGCACCA CCCTGCCCTTTACACTGGGCTTATGTTTAATCGGGGCTTCTGCCATTGCCACTTCCACGGCACCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56060778..56060876 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115011 RMVar_ID_115011 Human_SNP_ID_869067489 m1A Human chr7 - 141639362 141639362 141639362 AGTCTAGAAACACATGGATATTCTCCACTTTTAAAAATTCCATATTGACCCCATGTTTCTCTCAG AGTCTAGAAACACATGGATATTCTCCACTTTTCAAAATTCCATATTGACCCCATGTTTCTCTCAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:141639354..141639544 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 115012 RMVar_ID_115012 Human_SNP_ID_869069903 m1A Human chr7 - 128841142 128841142 128841142 GAAGCCTGGGGCAAGGTGGGGGAGGGTCGGGGATCCAGCATCAGGCAAGACCCTTCCGTCCCCCA GAAGCCTGGGGCAAGGTGGGGGAGGGTCGGGGGTCCAGCATCAGGCAAGACCCTTCCGTCCCCCA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:128841140..128841315 26863196 MeRIP-seq:(Medium) rs2291565 Functional Loss SNV ICGC 33..33 33 COCA 1 - 115013 RMVar_ID_115013 Human_SNP_ID_869073747 m1A Human chr7 + 5370367 5370367 5370367 ACTCACGAATCTGCAGAACTCAGAGGTCGCGCACTCTCACCTCCCATCTCTTGGCTCCTCCTCTC ACTCACGAATCTGCAGAACTCAGAGGTCGCGCGCTCTCACCTCCCATCTCTTGGCTCCTCCTCTC A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:5370365..5370472 26863196 MeRIP-seq:(Medium) rs1016775136 Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115014 RMVar_ID_115014 Human_SNP_ID_869098484 m1A Human chr7 + 30595030 30595030 30595030 CCCGACCCTCGCTCCTGCTCCGCCGGTCCCTCAGCGCGGCCTCCTGCCCCCCGATCTCCTTGCCC CCCGACCCTCGCTCCTGCTCCGCCGGTCCCTCCGCGCGGCCTCCTGCCCCCCGATCTCCTTGCCC A C GARS1 Ensembl:ENSG00000106105 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr7:30594876..30595176;chr7:30594876..30595193;chr7:30594876..30595213 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_793017,Human_RBP_ID_4939368,Human_RBP_ID_7732151,Human_RBP_ID_9337100,Human_RBP_ID_22112297,Human_RBP_ID_22534247,Human_RBP_ID_22834979 Human_miRNA_ID_2351471,Human_miRNA_ID_3047017 RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_106627,RMVar_hsa_circ_244361,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363 115015 RMVar_ID_115015 Human_SNP_ID_869105622 m1A Human chr7 - 2612719 2612719 2612719 CCCCTCCCATGACTAGGCCCCGCCCACAGCTCACCTCTCCCGTGACTAGGCCCCGCCCACAGCTC CCCCTCCCATGACTAGGCCCCGCCCACAGCTCCCCTCTCCCGTGACTAGGCCCCGCCCACAGCTC T G lnc-BRAT1-2,lnc-BRAT1-2:2 RNACentral:URS00008B7D3D,RNACentral:URS00008B91B7 lincRNA,lincRNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2612455..2612986 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 115016 RMVar_ID_115016 Human_SNP_ID_869109259 m1A Human chr7 - 100107461 100107461 100107461 CTCCCTCTGGTCCTGGGAGTGTCCAGAAGTACATCGTGGTCTCACTTCCCCCAACAGGGGAGGGC CTCCCTCTGGTCCTGGGAGTGTCCAGAAGTACTTCGTGGTCTCACTTCCCCCAACAGGGGAGGGC T A TAF6 Ensembl:ENSG00000106290 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100107410..100107640 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_691420,Human_RBP_ID_1690822,Human_RBP_ID_4955231,Human_RBP_ID_8675817 RMVar_hsa_circ_102089,RMVar_hsa_circ_247055 115017 RMVar_ID_115017 Human_SNP_ID_869115511 m1A Human chr7 - 44115875 44115875 44115875 GCTTTGCCTTGCAGATTTTTGGGGACATCAGGACAGAACGTGAGTGACATTTTCCGATACAGCAG GCTTTGCCTTGCAGATTTTTGGGGACATCAGGTCAGAACGTGAGTGACATTTTCCGATACAGCAG T A POLD2 Ensembl:ENSG00000106628 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44115790..44115893;chr7:44115826..44115900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_84023,Human_RBP_ID_1686801,Human_RBP_ID_2043131,Human_RBP_ID_3847130,Human_RBP_ID_16159983,Human_RBP_ID_18882968 Human_Splice_Rec_861738,Human_Splice_Rec_861760,Human_Splice_Rec_861780,Human_Splice_Rec_861800,Human_Splice_Rec_861808 Human_miRNA_ID_2996174 RMVar_hsa_circ_122099,RMVar_hsa_circ_122478,RMVar_hsa_circ_244917,RMVar_hsa_circ_244918 115018 RMVar_ID_115018 Human_SNP_ID_869118956 m1A Human chr7 - 152435749 152435743 152435749 GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCAGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGC______CGCCACCACCCCCCGAGGAGCCTGGAG GGCGGCT G KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152435703..152435783 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..38 33 ESCA 1 - Human_RBP_ID_252986,Human_RBP_ID_842694,Human_RBP_ID_19021665,Human_RBP_ID_23080479 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 115019 RMVar_ID_115019 Human_SNP_ID_869148165 m1A Human chr7 - 102638638 102638638 102638638 CGGGGCCCTTGGGCATTAACCCCTCCCTCTCTAGTTCCTCCCCGCCCGCCCCTGCCCACCTTCCA CGGGGCCCTTGGGCATTAACCCCTCCCTCTCTCGTTCCTCCCCGCCCGCCCCTGCCCACCTTCCA T G AC105052.1,AC105052.4,AC105052.3,UPK3BL1 Ensembl:ENSG00000205236,Ensembl:ENSG00000279168,Ensembl:ENSG00000267645,Ensembl:ENSG00000267368 Protein coding,lincRNA,Protein coding,Protein coding intron,intron,intron,intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs865881421 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_92342,RMVar_hsa_circ_247359,RMVar_hsa_circ_27262,RMVar_hsa_circ_81225,RMVar_hsa_circ_247369,RMVar_hsa_circ_119083,RMVar_hsa_circ_247371,RMVar_hsa_circ_247374,RMVar_hsa_circ_75925 115020 RMVar_ID_115020 Human_SNP_ID_869192373 m1A Human chr7 + 44118004 44118004 44118004 GCTGCAGCGGCATGGCCTTGAACAGAGTGCCCACCACACAGCACTTCTCCTCAGGCTGCAGTTCA GCTGCAGCGGCATGGCCTTGAACAGAGTGCCCTCCACACAGCACTTCTCCTCAGGCTGCAGTTCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:44117928..44118012 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 115021 RMVar_ID_115021 Human_SNP_ID_869216312 m1A Human chr7 + 88210916 88210916 88210916 CCAGCATTGAAACCATAAGCCGGCAAGTCTCCAGGTTAAAAGCTGTTAAATCAAGAAAAGTACAT CCAGCATTGAAACCATAAGCCGGCAAGTCTCCGGGTTAAAAGCTGTTAAATCAAGAAAAGTACAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:88210901..88210950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 115022 RMVar_ID_115022 Human_SNP_ID_869223258 m1A Human chr7 + 131587175 131587175 131587175 GTGTGTGTGATGAGTGTGGTGTGTGTAGTGTAAGTATGTGGTGCAGCATATATATGTGTGGTGTG GTGTGTGTGATGAGTGTGGTGTGTGTAGTGTACGTATGTGGTGCAGCATATATATGTGTGGTGTG A C RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:131587096..131587223 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_248571,RMVar_hsa_circ_248570 115023 RMVar_ID_115023 Human_SNP_ID_869281646 m1A Human chr7 - 2542747 2542747 2542747 GATGGCCTGCCAGTGTTCCAGGTGGGCTCACAATAGGGGTGGAAGTGACCTCAGGACCTGCTGCC GATGGCCTGCCAGTGTTCCAGGTGGGCTCACATTAGGGGTGGAAGTGACCTCAGGACCTGCTGCC T A BRAT1 Ensembl:ENSG00000106009 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:2542745..2542823 26863196 MeRIP-seq:(Medium) rs61673178 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_23075294,Human_RBP_ID_23259218,Human_RBP_ID_27842833 RMVar_hsa_circ_45891,RMVar_hsa_circ_124148,RMVar_hsa_circ_243368,RMVar_hsa_circ_243369,RMVar_hsa_circ_105410,RMVar_hsa_circ_122173,RMVar_hsa_circ_243370 115024 RMVar_ID_115024 Human_SNP_ID_869305759 m1A Human chr7 - 116862574 116862574 116862574 TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCAGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCGGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:116862526..116862699 26863196 MeRIP-seq:(Medium) rs192510686 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,COCA,large_intestine adenocarcinoma 4 caecum,large intestine 115025 RMVar_ID_115025 Human_SNP_ID_869318070 m1A Human chr7 - 76302741 76302741 76302741 CGCGGAAGGGGTCCCAGCTGGGGCCCCGCAGGAGCGAGAAGGGGACGCGGCGCTCGGTCATGCTG CGCGGAAGGGGTCCCAGCTGGGGCCCCGCAGGTGCGAGAAGGGGACGCGGCGCTCGGTCATGCTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:76302626..76303000 26863196 MeRIP-seq:(Medium) rs772216758 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary 115026 RMVar_ID_115026 Human_SNP_ID_869338880 m1A Human chr7 - 2540981 2540981 2540981 TGGAGTGCCTCGAGAGCCCCGGCTCCAGCCCCACGGTACGGTGGTGGGGATAGAGAGCGAGGAGA TGGAGTGCCTCGAGAGCCCCGGCTCCAGCCCCGCGGTACGGTGGTGGGGATAGAGAGCGAGGAGA T C BRAT1 Ensembl:ENSG00000106009 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2540963..2541113 32194978 MeRIP-seq:(Medium) rs1200261080 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_844034,Human_RBP_ID_19134580 Human_Splice_Rec_838646,Human_Splice_Rec_838647,Human_Splice_Rec_838672,Human_Splice_Rec_838690,Human_Splice_Rec_838697 RMVar_hsa_circ_124148,RMVar_hsa_circ_243368 115027 RMVar_ID_115027 Human_SNP_ID_869348387 m1A Human chr7 - 76482916 76482916 76482916 CAGAAGCGGTCCTGTGTGGGGGGTGCTGGGGGACGGGGTATGCAGGGAGGTTGGTCATGGAGTGG CAGAAGCGGTCCTGTGTGGGGGGTGCTGGGGGGCGGGGTATGCAGGGAGGTTGGTCATGGAGTGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:76482868..76483035 26863196 MeRIP-seq:(Medium) rs2270253 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV,skin mycosis_fungoides-Sezary_syndrome 12 skin,haematopoietic and lymphoid tissue,brain 115028 RMVar_ID_115028 Human_SNP_ID_869352835 m1A Human chr7 - 151519702 151519702 151519702 CCGGCCGGTCACGTGGGCGTGTTGTGGGGGGGAGGGGCGCCGCCGCGCGGTCGGTTCCGGGCGGT CCGGCCGGTCACGTGGGCGTGTTGTGGGGGGGGGGGGCGCCGCCGCGCGGTCGGTTCCGGGCGGT T C RHEB Ensembl:ENSG00000106615 Protein coding 5'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_174330 RMVar_hsa_circ_90529,RMVar_hsa_circ_249468 115029 RMVar_ID_115029 Human_SNP_ID_869361898 m1A Human chr7 - 1898351 1898351 1898351 GAAGCAGGTGGAGAGTGCCGAGCTGAAGAACCAGCGGCTCAAGGAGGTTTTCCAGACCAAGATCC GAAGCAGGTGGAGAGTGCCGAGCTGAAGAACCTGCGGCTCAAGGAGGTTTTCCAGACCAAGATCC T A MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:1898301..1898350 32194978 MeRIP-seq:(Medium) rs1193808551 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung Human_Splice_Rec_837972,Human_Splice_Rec_838004,Human_Splice_Rec_838040,Human_Splice_Rec_838076,Human_Splice_Rec_838092,Human_Splice_Rec_838098,Human_Splice_Rec_838226 RMVar_hsa_circ_35874,RMVar_hsa_circ_271154,RMVar_hsa_circ_285765,RMVar_hsa_circ_327846,RMVar_hsa_circ_364305,RMVar_hsa_circ_289069,RMVar_hsa_circ_276759,RMVar_hsa_circ_270626,RMVar_hsa_circ_243296,RMVar_hsa_circ_243297 115030 RMVar_ID_115030 Human_SNP_ID_869385786 m1A Human chr7 - 128759001 128759001 128759001 ACTACTATATCTTTCATGTAGTCATACTCCTCAGGGTGCAGGAAAGCTGTGAACTCCTCCTTGGT ACTACTATATCTTTCATGTAGTCATACTCCTCGGGGTGCAGGAAAGCTGTGAACTCCTCCTTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128758976..128759000 26863196 MeRIP-seq:(Medium) rs749617756 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 115031 RMVar_ID_115031 Human_SNP_ID_869386478 m1A Human chr7 - 6466270 6466270 6466270 TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTATTTATGATCAGCAAGACTGGGGAGGCCGAGAC TACCTGGAGTCCGTGGCTATCCTTCCGCAGCTGTTTATGATCAGCAAGACTGGGGAGGCCGAGAC T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2230263 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_RBP_ID_253472,Human_RBP_ID_17314452,Human_RBP_ID_17426891,Human_RBP_ID_17543174,Human_RBP_ID_21517222,Human_RBP_ID_22774275,Human_RBP_ID_24438899,Human_RBP_ID_24517036,Human_RBP_ID_26830184,Human_RBP_ID_27115550 Human_Splice_Rec_842180,Human_Splice_Rec_842184 Human_miRNA_ID_2611028,Human_miRNA_ID_2611029 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_243666,RMVar_hsa_circ_115442,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_91216,RMVar_hsa_circ_243667,RMVar_hsa_circ_243670,RMVar_hsa_circ_316068,RMVar_hsa_circ_343940,RMVar_hsa_circ_272548,RMVar_hsa_circ_243669 115032 RMVar_ID_115032 Human_SNP_ID_869391720 m1A Human chr7 + 6009333 6009333 6009333 CCTCTGACGGTTTCTGAGCGTTGGCCTTTGGCACGCGCTACCCCCTTTTGCTTTGGTTCTGCCAT CCTCTGACGGTTTCTGAGCGTTGGCCTTTGGCGCGCGCTACCCCCTTTTGCTTTGGTTCTGCCAT A G AIMP2 Ensembl:ENSG00000106305 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:6009251..6009445 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_RBP_ID_686345,Human_RBP_ID_4955643,Human_RBP_ID_16183176 Human_Splice_Rec_841583 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 115033 RMVar_ID_115033 Human_SNP_ID_869409575 m1A Human chr7 + 1542807 1542800 1542808 AGGGCGTGGGGACCCCGGCCCCCTATGCCGCCACGCCGCCACACCGCCTCACCCTGGCTTCTGTG AGGGCGTGGGGACCCCGGCCCCCTAT________GCCGCCACACCGCCTCACCCTGGCTTCTGTG TGCCGCCAC T MAFK Ensembl:ENSG00000198517 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:1542640..1543000 26863196 MeRIP-seq:(Medium) rs1051038467 Functional Loss DEL TCGA,ICGC 27..34 33 UCEC,ESCA 2 - 115034 RMVar_ID_115034 Human_SNP_ID_869444412 m1A Human chr7 - 102446696 102446696 102446696 CTCGATGTAGGGGTGCATGCGCTCATGCGGGGACTCGCTGATGGAGTTCAGGTTGTGGATGTTGC CTCGATGTAGGGGTGCATGCGCTCATGCGGGGGCTCGCTGATGGAGTTCAGGTTGTGGATGTTGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:102446646..102446748 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 115035 RMVar_ID_115035 Human_SNP_ID_869466799 m1A Human chr7 + 5529662 5529662 5529662 CGACGAGCGCGGCGATATCATCATCCATGGTGAGCTGCGAGAATAGCCGGGCGCGCTGTGAGCCG CGACGAGCGCGGCGATATCATCATCCATGGTGGGCTGCGAGAATAGCCGGGCGCGCTGTGAGCCG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906573,GSM1906574,GSM1906575,GSM1906576;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T cell line,total RNA;HEK293T,H2O2 treatment;HEK293T,Starvation treatment;HEK293T,untreat control chr7:5529576..5529716;chr7:5529601..5529729;chr7:5529576..5529722;chr7:5529576..5529729 26863196,26863410,26863410,26863410 MeRIP-seq:(Medium) rs1343972830 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115036 RMVar_ID_115036 Human_SNP_ID_869471292 m1A Human chr7 - 152135512 152135511 152135512 AACACAAAAATTTGAAAAAGTTAAAAAAAAAAAGGAGATGTGATTATGCTTACAGCTGCAGGACT AACACAAAAATTTGAAAAAGTTAAAAAAAAAA_GGAGATGTGATTATGCTTACAGCTGCAGGACT CT C KMT2C Ensembl:ENSG00000055609 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA,ICGC 33..33 33 UCEC,CESC,CHOL 12 - Human_RBP_ID_679304,Human_RBP_ID_24200540 Human_miRNA_ID_219166,Human_miRNA_ID_674820 RMVar_hsa_circ_249485,RMVar_hsa_circ_115161,RMVar_hsa_circ_93711,RMVar_hsa_circ_249484 115037 RMVar_ID_115037 Human_SNP_ID_869475901 m1A Human chr7 + 158871391 158871391 158871391 CAAAAGACCGGGAGAAAGAAAAGCTGAAGGAGAAACATCGAGAGGCAGAAAAGTCTCACAGCAGA CAAAAGACCGGGAGAAAGAAAAGCTGAAGGAGGAACATCGAGAGGCAGAAAAGTCTCACAGCAGA A G WDR60 Ensembl:ENSG00000126870 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:158856591..158901770 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 1 head and neck Human_RBP_ID_24236482,Human_RBP_ID_24549255,Human_RBP_ID_26357452 RMVar_hsa_circ_1244,RMVar_hsa_circ_69985,RMVar_hsa_circ_325007,RMVar_hsa_circ_378572,RMVar_hsa_circ_303490,RMVar_hsa_circ_308751,RMVar_hsa_circ_302059,RMVar_hsa_circ_58027,RMVar_hsa_circ_60480,RMVar_hsa_circ_51711,RMVar_hsa_circ_249932 115038 RMVar_ID_115038 Human_SNP_ID_869482704 m1A Human chr7 - 133895670 133895670 133895670 TGGAGCTTCACGCACACCATGTTGAGGAATTGATCTGAATATGCACTCAAGTCATGCATCAGGTT TGGAGCTTCACGCACACCATGTTGAGGAATTGTTCTGAATATGCACTCAAGTCATGCATCAGGTT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:133895620..133917616 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115039 RMVar_ID_115039 Human_SNP_ID_869515191 m1A Human chr7 - 148847298 148847298 148847298 TTTAATATGAAACCATTGCTTTTAGAATAATCATGGGCCAGACTGGGAAGAAATCTGAGAAGGGA TTTAATATGAAACCATTGCTTTTAGAATAATCGTGGGCCAGACTGGGAAGAAATCTGAGAAGGGA T C EZH2 Ensembl:ENSG00000106462 Protein coding start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr7:148847276..148847350 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue Human_RBP_ID_3836599,Human_RBP_ID_4960959,Human_RBP_ID_7710251,Human_RBP_ID_16059671,Human_RBP_ID_18426113,Human_RBP_ID_19021573,Human_RBP_ID_24198531,Human_RBP_ID_26082226 Human_Splice_Rec_935044,Human_Splice_Rec_935080,Human_Splice_Rec_935120,Human_Splice_Rec_935156,Human_Splice_Rec_935194,Human_Splice_Rec_935230,Human_Splice_Rec_935266,Human_Splice_Rec_935306,Human_Splice_Rec_935324 RMVar_hsa_circ_96943,RMVar_hsa_circ_327932,RMVar_hsa_circ_50935,RMVar_hsa_circ_354172,RMVar_hsa_circ_371414,RMVar_hsa_circ_249305,RMVar_hsa_circ_366592,RMVar_hsa_circ_342673,RMVar_hsa_circ_249312,RMVar_hsa_circ_347200,RMVar_hsa_circ_272332,RMVar_hsa_circ_249318,RMVar_hsa_circ_357813,RMVar_hsa_circ_249317,RMVar_hsa_circ_302655,RMVar_hsa_circ_249319,RMVar_hsa_circ_367884,RMVar_hsa_circ_285103,RMVar_hsa_circ_249322,RMVar_hsa_circ_249323,RMVar_hsa_circ_84815,RMVar_hsa_circ_274393,RMVar_hsa_circ_274419,RMVar_hsa_circ_249325,RMVar_hsa_circ_249326,RMVar_hsa_circ_280782,RMVar_hsa_circ_249328,RMVar_hsa_circ_79673,RMVar_hsa_circ_249327 115040 RMVar_ID_115040 Human_SNP_ID_869525711 m1A Human chr7 + 128092137 128092137 128092137 TTCCTCTGCCGGGAGGGTGTTTTCAACTCCAAACCCCAGAGAGGGGTTGTAGATTGGGTCCAGCT TTCCTCTGCCGGGAGGGTGTTTTCAACTCCAACCCCCAGAGAGGGGTTGTAGATTGGGTCCAGCT A C SND1 Ensembl:ENSG00000197157 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:128091980..128092200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_86341,Human_RBP_ID_5122900,Human_RBP_ID_17665114,Human_RBP_ID_26550775 Human_miRNA_ID_2424022,Human_miRNA_ID_2433682 RMVar_hsa_circ_76934,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_81641,RMVar_hsa_circ_248208 115041 RMVar_ID_115041 Human_SNP_ID_869528215 m1A Human chr7 - 23490661 23490661 23490661 CCTTGGCCAGGCCGTCCAGCTTGGTGACGGGCATCCGCTCCTTATCCTGGGCCTTGCCTCCGCGA CCTTGGCCAGGCCGTCCAGCTTGGTGACGGGCTTCCGCTCCTTATCCTGGGCCTTGCCTCCGCGA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23490553..23490802 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115042 RMVar_ID_115042 Human_SNP_ID_869538883 m1A Human chr7 - 99444804 99444804 99444804 TGCCGCAGGCAGCTTTCAAAAAGAATTCACAGACAGCAGCGCCCGACTCTGTAGAAAGGAGAGAA TGCCGCAGGCAGCTTTCAAAAAGAATTCACAGGCAGCAGCGCCCGACTCTGTAGAAAGGAGAGAA T C PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:99444776..99444850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach 115043 RMVar_ID_115043 Human_SNP_ID_869561483 m1A Human chr7 - 75738895 75738895 75738895 CGGCGACATGGATCGGATGGCCAGCTCCATGAAGCAGGTGCCCAACCCACTGCCCAAGGTGCTGA CGGCGACATGGATCGGATGGCCAGCTCCATGACGCAGGTGCCCAACCCACTGCCCAAGGTGCTGA T G HIP1 Ensembl:ENSG00000127946 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:75738846..75738944 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_4956424,Human_RBP_ID_23080081 Human_Splice_Rec_878495,Human_Splice_Rec_878551,Human_Splice_Rec_878677,Human_Splice_Rec_878679 Human_miRNA_ID_1013975,Human_miRNA_ID_1295976,Human_miRNA_ID_2461914,Human_miRNA_ID_2461915,Human_miRNA_ID_2634560,Human_miRNA_ID_2634561,Human_miRNA_ID_2637247,Human_miRNA_ID_2637248 115044 RMVar_ID_115044 Human_SNP_ID_869580285 m1A Human chr7 - 56064366 56064366 56064366 TGGACGGCCGGTTCACTGACCTAGCTTGAGCCACGCGCCGACCAGGAGCGACAGCAGGGGCAGCA TGGACGGCCGGTTCACTGACCTAGCTTGAGCCGCGCGCCGACCAGGAGCGACAGCAGGGGCAGCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:56064251..56064420 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115045 RMVar_ID_115045 Human_SNP_ID_869581443 m1A Human chr7 - 100686318 100686318 100686318 GGGTGTGGTGAAGAGGAGGGGCGGGGAGGGGGAGGCAGCTCTCACCTGCGGCGGTGCCGAGCGCC GGGTGTGGTGAAGAGGAGGGGCGGGGAGGGGGGGGCAGCTCTCACCTGCGGCGGTGCCGAGCGCC T C GIGYF1 Ensembl:ENSG00000146830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr7:100686149..100688310;chr7:100685326..100687425 26863196 MeRIP-seq:(Medium) rs1402661203 Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 2 stomach Human_RBP_ID_85014,Human_RBP_ID_253549,Human_RBP_ID_793621,Human_RBP_ID_844431,Human_RBP_ID_954747,Human_RBP_ID_3971165,Human_RBP_ID_5403283,Human_RBP_ID_8238301,Human_RBP_ID_8944181,Human_RBP_ID_9438959,Human_RBP_ID_19019979,Human_RBP_ID_22111044,Human_RBP_ID_22483045,Human_RBP_ID_22554872,Human_RBP_ID_22687156,Human_RBP_ID_22747112,Human_RBP_ID_23080378,Human_RBP_ID_23116903,Human_RBP_ID_24549217,Human_RBP_ID_24554962,Human_RBP_ID_26051409,Human_RBP_ID_26356844,Human_RBP_ID_26772081,Human_RBP_ID_27829621 Human_miRNA_ID_2241034 RMVar_hsa_circ_110960,RMVar_hsa_circ_102936,RMVar_hsa_circ_101130,RMVar_hsa_circ_93093,RMVar_hsa_circ_80604,RMVar_hsa_circ_247143,RMVar_hsa_circ_247144,RMVar_hsa_circ_247141,RMVar_hsa_circ_247142,RMVar_hsa_circ_247140,RMVar_hsa_circ_50574 115046 RMVar_ID_115046 Human_SNP_ID_869609792 m1A Human chr7 - 139093616 139093616 139093616 GGGGGTTGTTCTCTGGCGGGCAGGGGCCGGGGACACAAGGTGCTCAGTGGGGGAGCTTTTGAGCC GGGGGTTGTTCTCTGGCGGGCAGGGGCCGGGGGCACAAGGTGCTCAGTGGGGGAGCTTTTGAGCC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:139093594..139093727 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 115047 RMVar_ID_115047 Human_SNP_ID_869611512 m1A Human chr7 - 576974 576974 576974 GAGTTGGATGAGGCCGCTGATGGCGTTGGACGAGGCCGCTGATGGCGTTGGAAGATGCTCACCAC GAGTTGGATGAGGCCGCTGATGGCGTTGGACGGGGCCGCTGATGGCGTTGGAAGATGCTCACCAC T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr7:576886..577128 26863196 MeRIP-seq:(Medium) rs181752130 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_22728952 RMVar_hsa_circ_267663 115048 RMVar_ID_115048 Human_SNP_ID_869613065 m1A Human chr7 - 55019732 55019732 55019732 AGCGCGGGGCGCACGTGCGGGACCCCGGCCCCAGGCGCCCACCAGCACCCGGCTTTCGCCCACTG AGCGCGGGGCGCACGTGCGGGACCCCGGCCCCGGGCGCCCACCAGCACCCGGCTTTCGCCCACTG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:55019726..55019750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 7 prostate 115049 RMVar_ID_115049 Human_SNP_ID_869624316 m1A Human chr7 + 39950949 39950949 39950949 GGCGAGAGGCAAGAGGCGCGCAGGAGGGCGGCAGAAGCGGCGTCGCGGGCCCCGCGCCGGGCAGG GGCGAGAGGCAAGAGGCGCGCAGGAGGGCGGCGGAAGCGGCGTCGCGGGCCCCGCGCCGGGCAGG A G CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr7:39950926..39951025;chr7:39950926..39951082 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_RBP_ID_13769,Human_RBP_ID_5221346,Human_RBP_ID_26764957 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 115050 RMVar_ID_115050 Human_SNP_ID_869625043 m1A Human chr7 - 65979895 65979895 65979895 TCTCCTGTGTCTGCAGTGGGTGAATGGGGTCGACACGCTAGAGCATGAGGGGGGCTACCTCCCCT TCTCCTGTGTCTGCAGTGGGTGAATGGGGTCGGCACGCTAGAGCATGAGGGGGGCTACCTCCCCT T C GUSB Ensembl:ENSG00000169919 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:65979726..65979925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_793901 Human_Splice_Rec_870512,Human_Splice_Rec_870578,Human_Splice_Rec_870579,Human_Splice_Rec_870622,Human_Splice_Rec_870623,Human_Splice_Rec_870638 RMVar_hsa_circ_68586,RMVar_hsa_circ_285501,RMVar_hsa_circ_245310,RMVar_hsa_circ_77148,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245314,RMVar_hsa_circ_245313,RMVar_hsa_circ_303015,RMVar_hsa_circ_279899,RMVar_hsa_circ_245316,RMVar_hsa_circ_378530 115051 RMVar_ID_115051 Human_SNP_ID_869630672 m1A Human chr7 - 67025024 67025024 67025024 GAGCCAAGTGCAACATTTCCCAAAGTAACGGTACCTTTTCTTTCTTCACATGATCCATAATTTTG GAGCCAAGTGCAACATTTCCCAAAGTAACGGTGCCTTTTCTTTCTTCACATGATCCATAATTTTG T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:67024980..67025064 26863196 MeRIP-seq:(Medium) rs1332613958 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 115052 RMVar_ID_115052 Human_SNP_ID_869680193 m1A Human chr7 - 5529584 5529584 5529584 CGGCATGTGCAAGGCCGGCTTCGCGGGCGACGATGCCCCCCGGGCCGTCTTCCCCTCCATCGTGG CGGCATGTGCAAGGCCGGCTTCGCGGGCGACGGTGCCCCCCGGGCCGTCTTCCCCTCCATCGTGG T C ACTB Ensembl:ENSG00000075624 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr7:5529503..5529833;chr7:5529376..5529788;chr7:5529501..5529736;chr7:5529526..5529725 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 eye marginal_zone_lymphoma,haematopoietic_and_lymphoid_tissue marginal_zone_lymphoma 3 eye,haematopoietic and lymphoid tissue Human_RBP_ID_253034,Human_RBP_ID_686015,Human_RBP_ID_792845,Human_RBP_ID_956086,Human_RBP_ID_1052537,Human_RBP_ID_4945008,Human_RBP_ID_5479697,Human_RBP_ID_7746281,Human_RBP_ID_8669092,Human_RBP_ID_8911996,Human_RBP_ID_16179244,Human_RBP_ID_17713283,Human_RBP_ID_18102111,Human_RBP_ID_18883965,Human_RBP_ID_21513801,Human_RBP_ID_22324193,Human_RBP_ID_22463006,Human_RBP_ID_22516021,Human_RBP_ID_22534238,Human_RBP_ID_22835263,Human_RBP_ID_24516834,Human_RBP_ID_26725743,Human_RBP_ID_27114857,Human_RBP_ID_27161623,Human_RBP_ID_27358646 Human_Splice_Rec_840812,Human_Splice_Rec_840813,Human_Splice_Rec_840826,Human_Splice_Rec_840827,Human_Splice_Rec_840838,Human_Splice_Rec_840839,Human_Splice_Rec_840847,Human_Splice_Rec_840862,Human_Splice_Rec_840863,Human_Splice_Rec_840874,Human_Splice_Rec_840877,Human_Splice_Rec_840882,Human_Splice_Rec_840883,Human_Splice_Rec_840889,Human_Splice_Rec_840896,Human_Splice_Rec_840897,Human_Splice_Rec_840902,Human_Splice_Rec_840904,Human_Splice_Rec_840905,Human_Splice_Rec_840908,Human_Splice_Rec_840909,Human_Splice_Rec_840914,Human_Splice_Rec_840915 Human_miRNA_ID_3057203 RMVar_hsa_circ_110714,RMVar_hsa_circ_126855,RMVar_hsa_circ_243503,RMVar_hsa_circ_243504,RMVar_hsa_circ_105019,RMVar_hsa_circ_88728,RMVar_hsa_circ_123677,RMVar_hsa_circ_243511,RMVar_hsa_circ_243512,RMVar_hsa_circ_98171,RMVar_hsa_circ_243514,RMVar_hsa_circ_373642,RMVar_hsa_circ_243516,RMVar_hsa_circ_243517,RMVar_hsa_circ_243518,RMVar_hsa_circ_376287 115053 RMVar_ID_115053 Human_SNP_ID_869686931 m1A Human chr7 + 100344860 100344860 100344860 AAGACACAAGACAAAGAGATAGAAGAAAAGACAGCTGGGCCAGGGGGACCACTACCACCTAGACG AAGACACAAGACAAAGAGATAGAAGAAAAGACTGCTGGGCCAGGGGGACCACTACCACCTAGACG A T STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100344810..100344895 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_16271333,Human_RBP_ID_17427777,Human_RBP_ID_18888796 RMVar_hsa_circ_79948,RMVar_hsa_circ_247085,RMVar_hsa_circ_48532,RMVar_hsa_circ_87828,RMVar_hsa_circ_369204,RMVar_hsa_circ_85580,RMVar_hsa_circ_90332,RMVar_hsa_circ_247086,RMVar_hsa_circ_247087,RMVar_hsa_circ_59978,RMVar_hsa_circ_247088 115054 RMVar_ID_115054 Human_SNP_ID_869691890 m1A Human chr7 + 5528505 5528503 5528506 CCGTGGTGGTGAAGCTGTAGCCGCGCTCGGTGAGGATCTTCATGAGGTAGTCAGTCAGGTCCCGG CCGTGGTGGTGAAGCTGTAGCCGCGCTCGGT___GATCTTCATGAGGTAGTCAGTCAGGTCCCGG TGAG T - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr7:5528275..5528712;chr7:5528264..5528721;chr7:5528294..5528750;chr7:5528317..5528719 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 STAD 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115055 RMVar_ID_115055 Human_SNP_ID_869697700 m1A Human chr7 - 26193677 26193648 26193678 CTTATTTTATAATAGGTGGCAATTTTGGAGGTAGCCCCGGTTATGGAGGAGGAAGAGGAGGATAT CTTATTTTATAATAGGTGGCAATTTTGGAGG______________________________ATAT TCCTCCTCTTCCTCCTCCATAACCGGGGCTA T HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:26193571..26193742 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..61 33 STAD 1 - Human_RBP_ID_14354,Human_RBP_ID_84110,Human_RBP_ID_253292,Human_RBP_ID_681748,Human_RBP_ID_793272,Human_RBP_ID_844467,Human_RBP_ID_1051621,Human_RBP_ID_1070150,Human_RBP_ID_1143752,Human_RBP_ID_1220962,Human_RBP_ID_2040464,Human_RBP_ID_3082730,Human_RBP_ID_3842083,Human_RBP_ID_4936416,Human_RBP_ID_7727115,Human_RBP_ID_8910395,Human_RBP_ID_9209573,Human_RBP_ID_9403225,Human_RBP_ID_16124336,Human_RBP_ID_17425119,Human_RBP_ID_18098035,Human_RBP_ID_18451528,Human_RBP_ID_19020635,Human_RBP_ID_22463912,Human_RBP_ID_23080628,Human_RBP_ID_23120481,Human_RBP_ID_23139985,Human_RBP_ID_24549102,Human_RBP_ID_26356336,Human_RBP_ID_26724167,Human_RBP_ID_27111213,Human_RBP_ID_27767188,Human_RBP_ID_27829222,Human_RBP_ID_27842871 Human_Splice_Rec_851106,Human_Splice_Rec_851130,Human_Splice_Rec_851150,Human_Splice_Rec_851172,Human_Splice_Rec_851192,Human_Splice_Rec_851210,Human_Splice_Rec_851228 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_68397,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_244220,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_244226 115056 RMVar_ID_115056 Human_SNP_ID_869702459 m1A Human chr7 + 45917362 45917362 45917362 CTTTGAATGGAGGGGGTGGAACTTGGGATCAGACACCCGGTGCGTGCTGGAGACGGACGGGCTCT CTTTGAATGGAGGGGGTGGAACTTGGGATCAGCCACCCGGTGCGTGCTGGAGACGGACGGGCTCT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:45917201..45917450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115057 RMVar_ID_115057 Human_SNP_ID_869710544 m1A Human chr7 + 105203670 105203670 105203670 GTCCGCAGGGTCCTCTTGCTCCTCATCATCTGATCCCAGGATCTCCTCCTCTGGCTCCGGGGGTG GTCCGCAGGGTCCTCTTGCTCCTCATCATCTGTTCCCAGGATCTCCTCCTCTGGCTCCGGGGGTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:105203630..105203731 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver 115058 RMVar_ID_115058 Human_SNP_ID_869762221 m1A Human chr7 - 19117110 19117110 19117110 CGGAGGCGGCGACGAGCCGGGCAGCCCGGCCCAGGGCAAGCGCGGCAAGAAGTCTGCGGGCTGTG CGGAGGCGGCGACGAGCCGGGCAGCCCGGCCCGGGGCAAGCGCGGCAAGAAGTCTGCGGGCTGTG T C TWIST1 Ensembl:ENSG00000122691 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:19117060..19117155 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4934740 115059 RMVar_ID_115059 Human_SNP_ID_869773585 m1A Human chr7 + 26864514 26864514 26864514 ACGGGGTGGGGCTGCGGCTGCGACCTAGACTCAGGCTAGCGGCCCGGATTAAGAACAGCGGGGCT ACGGGGTGGGGCTGCGGCTGCGACCTAGACTCGGGCTAGCGGCCCGGATTAAGAACAGCGGGGCT A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:26864416..26864550 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 115060 RMVar_ID_115060 Human_SNP_ID_869780099 m1A Human chr7 - 44696963 44696963 44696963 AACGCCATGTACTCCGCTAGAGCCCAGTCCACAGTCCGGTTCTTCACCATTTCCCCACGAGTCTT AACGCCATGTACTCCGCTAGAGCCCAGTCCACGGTCCGGTTCTTCACCATTTCCCCACGAGTCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:44696899..44697021 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 13 ovary 115061 RMVar_ID_115061 Human_SNP_ID_869781267 m1A Human chr7 + 100819881 100819881 100819881 GTTCAGGCGGGAAACCACGCTCCGCGGAGCCGAAGGAGGGGCTGCAGGAGACCAGGGAGTCAGGC GTTCAGGCGGGAAACCACGCTCCGCGGAGCCGGAGGAGGGGCTGCAGGAGACCAGGGAGTCAGGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100819661..100819912 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115062 RMVar_ID_115062 Human_SNP_ID_869782820 m1A Human chr7 + 30599999 30599999 30599999 AGATGATATTGTAGACCGAGCAAAAATGGAAGATACCCTGAAGAGGAGGTTTTTCTATGATCAAG AGATGATATTGTAGACCGAGCAAAAATGGAAGGTACCCTGAAGAGGAGGTTTTTCTATGATCAAG A G GARS1 Ensembl:ENSG00000106105 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:30599890..30599999 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_683103,Human_RBP_ID_1686052,Human_RBP_ID_2041482,Human_RBP_ID_3843971,Human_RBP_ID_7732188,Human_RBP_ID_9210255,Human_RBP_ID_16137322,Human_RBP_ID_18099117,Human_RBP_ID_19019507,Human_RBP_ID_23076255,Human_RBP_ID_24211730 Human_Splice_Rec_853802,Human_Splice_Rec_853803,Human_Splice_Rec_853810,Human_Splice_Rec_853811,Human_Splice_Rec_853840,Human_Splice_Rec_853841 Human_miRNA_ID_1137210,Human_miRNA_ID_1139726 RMVar_hsa_circ_11800,RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_106627,RMVar_hsa_circ_318343,RMVar_hsa_circ_244361,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363,RMVar_hsa_circ_337059,RMVar_hsa_circ_360671,RMVar_hsa_circ_322693,RMVar_hsa_circ_33073,RMVar_hsa_circ_33440,RMVar_hsa_circ_25027,RMVar_hsa_circ_61702,RMVar_hsa_circ_244364,RMVar_hsa_circ_244365,RMVar_hsa_circ_94406,RMVar_hsa_circ_374938,RMVar_hsa_circ_244366,RMVar_hsa_circ_244367 115063 RMVar_ID_115063 Human_SNP_ID_869785111 m1A Human chr7 + 100888067 100888067 100888067 CGTGTTGTACTCCCCCCAGGTTTGACCCCAGGACTCCCCTACCCACACCAGACTCCCCAGGGCCT CGTGTTGTACTCCCCCCAGGTTTGACCCCAGGTCTCCCCTACCCACACCAGACTCCCCAGGGCCT A T SRRT Ensembl:ENSG00000087087 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100888051..100888075 26863196 MeRIP-seq:(Medium) rs1010301297 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_83181,Human_RBP_ID_1049529,Human_RBP_ID_3972311,Human_RBP_ID_5123075,Human_RBP_ID_7666691,Human_RBP_ID_9309967,Human_RBP_ID_15946296,Human_RBP_ID_18087369,Human_RBP_ID_18872637,Human_RBP_ID_22111059,Human_RBP_ID_23070024,Human_RBP_ID_24180268,Human_RBP_ID_26131139,Human_RBP_ID_27830614 Human_Splice_Rec_901509,Human_Splice_Rec_901548,Human_Splice_Rec_901549,Human_Splice_Rec_901585,Human_Splice_Rec_901630,Human_Splice_Rec_901631,Human_Splice_Rec_901675,Human_Splice_Rec_901695 Human_miRNA_ID_2039653,Human_miRNA_ID_3018635 RMVar_hsa_circ_34585,RMVar_hsa_circ_111923,RMVar_hsa_circ_247197,RMVar_hsa_circ_112797,RMVar_hsa_circ_95915,RMVar_hsa_circ_247198,RMVar_hsa_circ_105326,RMVar_hsa_circ_247200,RMVar_hsa_circ_247201,RMVar_hsa_circ_247202,RMVar_hsa_circ_103465,RMVar_hsa_circ_247204,RMVar_hsa_circ_84464,RMVar_hsa_circ_85025,RMVar_hsa_circ_101490,RMVar_hsa_circ_247206,RMVar_hsa_circ_92040,RMVar_hsa_circ_247207,RMVar_hsa_circ_247208,RMVar_hsa_circ_24126,RMVar_hsa_circ_247210 115064 RMVar_ID_115064 Human_SNP_ID_869792806 m1A Human chr7 - 40134422 40134422 40134422 GCCCTCCCCTCGAGACGGGTACGGGAGTCCGCACCACACGCCGCCGTACGGGCCCCGGTCTAGGC GCCCTCCCCTCGAGACGGGTACGGGAGTCCGCCCCACACGCCGCCGTACGGGCCCCGGTCTAGGC T G MPLKIP Ensembl:ENSG00000168303 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:40134226..40134558 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_18100140,Human_RBP_ID_22463049 115065 RMVar_ID_115065 Human_SNP_ID_869801764 m1A Human chr7 - 97854597 97854597 97854597 CTCTATTTGTTTGATGTTCTCCGCGCAGATCGAACTACTGCTGCCCATGGGTAATATTTTTAGAG CTCTATTTGTTTGATGTTCTCCGCGCAGATCGCACTACTGCTGCCCATGGGTAATATTTTTAGAG T G AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding exon,CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma,breast HER-positive_carcinoma 15 breast Human_RBP_ID_792494,Human_RBP_ID_1144605,Human_RBP_ID_1689939,Human_RBP_ID_2049715,Human_RBP_ID_3858971,Human_RBP_ID_4965849,Human_RBP_ID_5513830,Human_RBP_ID_5625145,Human_RBP_ID_7774867,Human_RBP_ID_8674830,Human_RBP_ID_8913307,Human_RBP_ID_16258719,Human_RBP_ID_18451985,Human_RBP_ID_18887708,Human_RBP_ID_22516323,Human_RBP_ID_22774670,Human_RBP_ID_24233257,Human_RBP_ID_27118058 Human_Splice_Rec_892994,Human_Splice_Rec_892995,Human_Splice_Rec_893020,Human_Splice_Rec_893021,Human_Splice_Rec_893044,Human_Splice_Rec_893045,Human_Splice_Rec_893067,Human_Splice_Rec_893086,Human_Splice_Rec_893087,Human_Splice_Rec_893108,Human_Splice_Rec_893109,Human_Splice_Rec_893128,Human_Splice_Rec_893129,Human_Splice_Rec_893152,Human_Splice_Rec_893153,Human_Splice_Rec_893159,Human_Splice_Rec_893230,Human_Splice_Rec_893231,Human_Splice_Rec_893264,Human_Splice_Rec_893265,Human_Splice_Rec_893286,Human_Splice_Rec_893287 Human_miRNA_ID_831533,Human_miRNA_ID_2173374,Human_miRNA_ID_2176818,Human_miRNA_ID_2355313,Human_miRNA_ID_3159973,Human_miRNA_ID_3160177,Human_miRNA_ID_3170598 RMVar_hsa_circ_21947,RMVar_hsa_circ_108188,RMVar_hsa_circ_246747 115066 RMVar_ID_115066 Human_SNP_ID_869806224 m1A Human chr7 + 151064336 151064336 151064336 CAGGAGGCCGGGTCTCGTGGAGGGGAGGAGCCAGGCCGCAGCTATGGGGAGGAAGACTTTGAGTG CAGGAGGCCGGGTCTCGTGGAGGGGAGGAGCCTGGCCGCAGCTATGGGGAGGAAGACTTTGAGTG A T SLC4A2 Ensembl:ENSG00000164889 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:151064177..151064385 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_253685,Human_RBP_ID_678812,Human_RBP_ID_793817,Human_RBP_ID_3971550,Human_RBP_ID_9312071,Human_RBP_ID_22621963,Human_RBP_ID_23080469,Human_RBP_ID_24554991,Human_RBP_ID_26357290 Human_Splice_Rec_938021,Human_Splice_Rec_938029,Human_Splice_Rec_938073,Human_Splice_Rec_938121,Human_Splice_Rec_938129,Human_Splice_Rec_938135,Human_Splice_Rec_938141,Human_Splice_Rec_938183 Human_miRNA_ID_2083113 RMVar_hsa_circ_58653,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416 115067 RMVar_ID_115067 Human_SNP_ID_869819804 m1A Human chr7 - 102531288 102531288 102531288 AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAAAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA AGAAAGAGAGAGGAGAGGGAGAGGGAGAAAGAGAGGGGGGGGGGGAGAGAGAGAGAGATGAAAGA T C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:102531239..102531327;chr7:102531236..102531329;chr7:102531229..102531323 26863196 MeRIP-seq:(Medium) rs1286392688 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 115068 RMVar_ID_115068 Human_SNP_ID_869842891 m1A Human chr7 + 102248500 102248500 102248500 AGGCGGGCGCCAGCGACTCACCCTCGGCCCGCAGCGGCCGGGCGGCGCCCAGCTCGGAGGGCGAC AGGCGGGCGCCAGCGACTCACCCTCGGCCCGCTGCGGCCGGGCGGCGCCCAGCTCGGAGGGCGAC A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr7:102248451..102248653;chr7:102248457..102248748 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 14 lung Human_RBP_ID_9311414 Human_Splice_Rec_902652,Human_Splice_Rec_902694,Human_Splice_Rec_902926,Human_Splice_Rec_903014,Human_Splice_Rec_903060,Human_Splice_Rec_903104,Human_Splice_Rec_903146,Human_Splice_Rec_903188 RMVar_hsa_circ_85687,RMVar_hsa_circ_247267,RMVar_hsa_circ_267024,RMVar_hsa_circ_264945,RMVar_hsa_circ_266127,RMVar_hsa_circ_87521,RMVar_hsa_circ_247291 115069 RMVar_ID_115069 Human_SNP_ID_869856903 m1A Human chr7 - 44765496 44765496 44765496 CAAAGGGGGCAGCGCCGGGGCCCAGGGCGGCGATCATCTCCATCACGCTGGGCATGAGCACGTGG CAAAGGGGGCAGCGCCGGGGCCCAGGGCGGCGTTCATCTCCATCACGCTGGGCATGAGCACGTGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr7:44765351..44765610;chr7:44765449..44765588;chr7:44765326..44765575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 115070 RMVar_ID_115070 Human_SNP_ID_869860336 m1A Human chr7 - 100093354 100093354 100093354 GTGGATGTGGTGGAGAAAGAAGATGTGAATGAAGCCATCAGGCTAATGGAGATGTCAAAGGACTC GTGGATGTGGTGGAGAAAGAAGATGTGAATGACGCCATCAGGCTAATGGAGATGTCAAAGGACTC T G MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100093269..100093386 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 4 lung Human_RBP_ID_85504,Human_RBP_ID_1690704,Human_RBP_ID_2050376,Human_RBP_ID_3860068,Human_RBP_ID_3971072,Human_RBP_ID_5220046,Human_RBP_ID_8272047,Human_RBP_ID_8675728,Human_RBP_ID_8914100,Human_RBP_ID_9404728,Human_RBP_ID_17314365,Human_RBP_ID_17426811,Human_RBP_ID_17543123,Human_RBP_ID_18107798,Human_RBP_ID_18171934,Human_RBP_ID_18888635,Human_RBP_ID_23081926,Human_RBP_ID_24234924 Human_Splice_Rec_896880,Human_Splice_Rec_896881,Human_Splice_Rec_896908,Human_Splice_Rec_896909,Human_Splice_Rec_896934,Human_Splice_Rec_896935,Human_Splice_Rec_896960,Human_Splice_Rec_896961,Human_Splice_Rec_897002,Human_Splice_Rec_897003,Human_Splice_Rec_897010,Human_Splice_Rec_897014 Human_miRNA_ID_259401,Human_miRNA_ID_263196,Human_miRNA_ID_1413154,Human_miRNA_ID_1543902,Human_miRNA_ID_1596736,Human_miRNA_ID_2042875,Human_miRNA_ID_2042876,Human_miRNA_ID_2045026,Human_miRNA_ID_2045027,Human_miRNA_ID_2047256,Human_miRNA_ID_2047257 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,RMVar_hsa_circ_101507,RMVar_hsa_circ_107157,RMVar_hsa_circ_112139,RMVar_hsa_circ_123162,RMVar_hsa_circ_111868,RMVar_hsa_circ_106455,RMVar_hsa_circ_92119,RMVar_hsa_circ_96816,RMVar_hsa_circ_91138,RMVar_hsa_circ_247010,RMVar_hsa_circ_247014,RMVar_hsa_circ_247018,RMVar_hsa_circ_76034,RMVar_hsa_circ_76156,RMVar_hsa_circ_247020,RMVar_hsa_circ_247021,RMVar_hsa_circ_247019,RMVar_hsa_circ_247016,RMVar_hsa_circ_247017,RMVar_hsa_circ_247015,RMVar_hsa_circ_247012,RMVar_hsa_circ_247013,RMVar_hsa_circ_247011,RMVar_hsa_circ_76250,RMVar_hsa_circ_49459,RMVar_hsa_circ_247022 115071 RMVar_ID_115071 Human_SNP_ID_869860500 m1A Human chr7 + 100676798 100676798 100676798 AGATCTATGCCATGCACTGGGGGACCGACTCAAGGTGTGTGTGTGTGCGCGGGCTGGCGCTGTGG AGATCTATGCCATGCACTGGGGGACCGACTCACGGTGTGTGTGTGTGCGCGGGCTGGCGCTGTGG A C GNB2 Ensembl:ENSG00000172354 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100676662..100676845 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_954737,Human_RBP_ID_1049473,Human_RBP_ID_5404382,Human_RBP_ID_19135273,Human_RBP_ID_24180146,Human_RBP_ID_26830623 Human_Splice_Rec_900025,Human_Splice_Rec_900041,Human_Splice_Rec_900057,Human_Splice_Rec_900073,Human_Splice_Rec_900113,Human_Splice_Rec_900131,Human_Splice_Rec_900143,Human_Splice_Rec_900153 115072 RMVar_ID_115072 Human_SNP_ID_869864731 m1A Human chr7 - 100100095 100100095 100100095 TTTGTGTCTTACGGTTTTACATTTCATGTTACAGAAAAGGTTAAGAAGTTCTTACAAGAGTTCTA TTTGTGTCTTACGGTTTTACATTTCATGTTACGGAAAAGGTTAAGAAGTTCTTACAAGAGTTCTA T C MCM7 Ensembl:ENSG00000166508 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100100051..100100100 32194978 MeRIP-seq:(Medium) rs762955038 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COCA,LIHC,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 10 liver,large intestine Human_RBP_ID_26129447 Human_Splice_Rec_896859,Human_Splice_Rec_896885,Human_Splice_Rec_896913,Human_Splice_Rec_896939,Human_Splice_Rec_896965,Human_Splice_Rec_896981,Human_Splice_Rec_897017,Human_Splice_Rec_897025,Human_Splice_Rec_897037,Human_Splice_Rec_897041,Human_Splice_Rec_897043 RMVar_hsa_circ_112139,RMVar_hsa_circ_247021,RMVar_hsa_circ_113385,RMVar_hsa_circ_247031,RMVar_hsa_circ_91352,RMVar_hsa_circ_247040 115073 RMVar_ID_115073 Human_SNP_ID_869897060 m1A Human chr7 - 42932423 42932423 42932423 GTAGTTTCGAAGCACTCCCCGGGCCGCAGACCACGGCGAAACCACCAAGACCAGCATGGCCAGCG GTAGTTTCGAAGCACTCCCCGGGCCGCAGACCTCGGCGAAACCACCAAGACCAGCATGGCCAGCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:42932351..42932479 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 2 lung 115074 RMVar_ID_115074 Human_SNP_ID_869903871 m1A Human chr7 + 44123509 44123509 44123509 CCCAGCTGACCCCGTTTCCCTGGACCCCACTCACCGCGCGGCGCGCCGCATCCCGCCAATCCCCG CCCAGCTGACCCCGTTTCCCTGGACCCCACTCCCCGCGCGGCGCGCCGCATCCCGCCAATCCCCG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:44123501..44123550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung 115075 RMVar_ID_115075 Human_SNP_ID_869904232 m1A Human chr7 - 26196558 26196555 26196558 CAGGAAGTTCAGAGTTCTAGGAGTGGAAGAGGAGGTAATTTTAATTCTGTTTCTTCTTTATTTTT CAGGAAGTTCAGAGTTCTAGGAGTGGAAGAGG___TAATTTTAATTCTGTTTCTTCTTTATTTTT ACCT A HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:26196551..26196575 26863196 MeRIP-seq:(Medium) rs902316320 Functional Loss DEL TCGA,ICGC 33..35 33 GBM 2 - Human_RBP_ID_253297,Human_RBP_ID_681764,Human_RBP_ID_793280,Human_RBP_ID_844469,Human_RBP_ID_2040495,Human_RBP_ID_3842103,Human_RBP_ID_5622860,Human_RBP_ID_7727187,Human_RBP_ID_8271882,Human_RBP_ID_8665215,Human_RBP_ID_16124519,Human_RBP_ID_23075554,Human_RBP_ID_24209052,Human_RBP_ID_26137165,Human_RBP_ID_26356347 Human_Splice_Rec_851101,Human_Splice_Rec_851125,Human_Splice_Rec_851167,Human_Splice_Rec_851187,Human_Splice_Rec_851205,Human_Splice_Rec_851223,Human_Splice_Rec_851237 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_374972,RMVar_hsa_circ_366603,RMVar_hsa_circ_244219,RMVar_hsa_circ_338242,RMVar_hsa_circ_61069,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_355365,RMVar_hsa_circ_363221,RMVar_hsa_circ_351112,RMVar_hsa_circ_71972,RMVar_hsa_circ_244229,RMVar_hsa_circ_64666,RMVar_hsa_circ_244228,RMVar_hsa_circ_65130,RMVar_hsa_circ_350895,RMVar_hsa_circ_353579,RMVar_hsa_circ_373388,RMVar_hsa_circ_244230 115076 RMVar_ID_115076 Human_SNP_ID_869908066 m1A Human chr7 - 140472000 140472000 140472000 TTGTGGTCTTTCGTCTCACAGGTATTTTATGCATGGGGTTTGTAAGGAAGGAGACAACTGTCGCT TTGTGGTCTTTCGTCTCACAGGTATTTTATGCGTGGGGTTTGTAAGGAAGGAGACAACTGTCGCT T C MKRN1 Ensembl:ENSG00000133606 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:140471926..140472226 26863196 MeRIP-seq:(Medium) rs572012392 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_677472,Human_RBP_ID_1682700,Human_RBP_ID_4960624,Human_RBP_ID_7706024,Human_RBP_ID_16045133,Human_RBP_ID_18108236,Human_RBP_ID_18877251,Human_RBP_ID_22686015,Human_RBP_ID_24196231 Human_Splice_Rec_929410,Human_Splice_Rec_929424,Human_Splice_Rec_929436,Human_Splice_Rec_929446,Human_Splice_Rec_929470,Human_Splice_Rec_929478,Human_Splice_Rec_929486,Human_Splice_Rec_929494,Human_Splice_Rec_929502,Human_Splice_Rec_929508,Human_Splice_Rec_929524,Human_Splice_Rec_929532,Human_Splice_Rec_929536 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662,RMVar_hsa_circ_295560 115077 RMVar_ID_115077 Human_SNP_ID_869912309 m1A Human chr7 + 158980723 158980723 158980723 CCACAGAGGTTGTGACATCACCTCAGGGTCCAAGACGTGCTTCCTAGGGGCCCCCTGGCGGTCTC CCACAGAGGTTGTGACATCACCTCAGGGTCCAGGACGTGCTTCCTAGGGGCCCCCTGGCGGTCTC A G lnc-WDR60-3 RNACentral:URS00008BE388 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:158980675..158980807 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115078 RMVar_ID_115078 Human_SNP_ID_869927963 m1A Human chr7 + 74700370 74700370 74700370 AGGTGTTGCCTTTAAACACCCCGAGAACTATGATCTTGCAACCCTGAAATGGATTTTGGAGAACA AGGTGTTGCCTTTAAACACCCCGAGAACTATGGTCTTGCAACCCTGAAATGGATTTTGGAGAACA A G GTF2I Ensembl:ENSG00000263001 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:74699016..74705171 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 5 biliary tract,gallbladder Human_RBP_ID_2046828,Human_RBP_ID_3852507,Human_RBP_ID_3970957,Human_RBP_ID_9403492,Human_RBP_ID_16217455,Human_RBP_ID_26356567,Human_RBP_ID_27116554 Human_Splice_Rec_876725,Human_Splice_Rec_876795,Human_Splice_Rec_876863,Human_Splice_Rec_876929,Human_Splice_Rec_876995,Human_Splice_Rec_877059 Human_miRNA_ID_2293854,Human_miRNA_ID_2293855 RMVar_hsa_circ_4302,RMVar_hsa_circ_58091,RMVar_hsa_circ_297141,RMVar_hsa_circ_329949,RMVar_hsa_circ_338708,RMVar_hsa_circ_290354,RMVar_hsa_circ_44246,RMVar_hsa_circ_52836,RMVar_hsa_circ_30342,RMVar_hsa_circ_65568,RMVar_hsa_circ_16714,RMVar_hsa_circ_294625,RMVar_hsa_circ_3820,RMVar_hsa_circ_359289,RMVar_hsa_circ_70405,RMVar_hsa_circ_32488 115079 RMVar_ID_115079 Human_SNP_ID_869932819 m1A Human chr7 + 149838633 149838633 149838633 AAAGCGGGGCCATGGAGCCCAGAGAGTCGGGGAAGGTAGGACTGGAAGGCCCGGGGGCCGCCCGC AAAGCGGGGCCATGGAGCCCAGAGAGTCGGGGGAGGTAGGACTGGAAGGCCCGGGGGCCGCCCGC A G ZNF862 Ensembl:ENSG00000106479 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:149838537..149838699 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_254202 Human_Splice_Rec_936259 115080 RMVar_ID_115080 Human_SNP_ID_869940319 m1A Human chr7 - 44582134 44582134 44582134 GGCAGGCCCTGCTGCTTCTCGCGCTGTGCGCCACAGGCGCCCAGGGGCTCTACTTCCACATCGGC GGCAGGCCCTGCTGCTTCTCGCGCTGTGCGCCGCAGGCGCCCAGGGGCTCTACTTCCACATCGGC T C TMED4 Ensembl:ENSG00000158604 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44582051..44582225 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_684785,Human_RBP_ID_1052145,Human_RBP_ID_4955760,Human_RBP_ID_5327835,Human_RBP_ID_9211366,Human_RBP_ID_22323499,Human_RBP_ID_22463476 Human_Splice_Rec_863149,Human_Splice_Rec_863155,Human_Splice_Rec_863161,Human_Splice_Rec_863171 115081 RMVar_ID_115081 Human_SNP_ID_869951525 m1A Human chr7 + 128794403 128794403 128794403 TATGAGGAGGAAGAGGAAGAGGAAGAGGAGGAAGAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA TATGAGGAGGAAGAGGAAGAGGAAGAGGAGGAGGAAGAGGTGGAAGAAGAAGAAGAACAAGTGCA A G CCDC136 Ensembl:ENSG00000128596 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:128794323..128794537 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 10 ovary Human_RBP_ID_14573,Human_RBP_ID_1690977,Human_RBP_ID_3971362,Human_RBP_ID_18414232,Human_RBP_ID_22621467,Human_RBP_ID_22685896,Human_RBP_ID_23080161,Human_RBP_ID_24549032,Human_RBP_ID_26358326,Human_RBP_ID_27829820 Human_Splice_Rec_920682,Human_Splice_Rec_920692,Human_Splice_Rec_920698,Human_Splice_Rec_920716,Human_Splice_Rec_920736,Human_Splice_Rec_920738,Human_Splice_Rec_920772 115082 RMVar_ID_115082 Human_SNP_ID_869958187 m1A Human chr7 - 133035836 133035836 133035836 CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGATCCGCGTGCTCTCCGCACCACCCCACTTCCAT CTCTCATCGCTGCTCAGTACAGCGGGGCTCAGGTCCGCGTGCTCTCCGCACCACCCCACTTCCAT T C CHCHD3,AC008038.1 Ensembl:ENSG00000106554,Ensembl:ENSG00000283041 Protein coding,Pseudogene intron,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs12674366 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_9217693 Human_miRNA_ID_1855106,Human_miRNA_ID_1856247 RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_300564,RMVar_hsa_circ_341277 115083 RMVar_ID_115083 Human_SNP_ID_869961728 m1A Human chr7 - 143876369 143876369 143876369 GAAGCCCAGCTCACGCCCTTTCTCCTGAACGCAGTGGGGTGGCTTTGCTCTTCCCCTGGGGCTCC GAAGCCCAGCTCACGCCCTTTCTCCTGAACGCTGTGGGGTGGCTTTGCTCTTCCCCTGGGGCTCC T A TCAF1 Ensembl:ENSG00000198420 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:143876274..143876374 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_678137,Human_RBP_ID_4929303,Human_RBP_ID_9311588,Human_RBP_ID_22111317,Human_RBP_ID_22515346,Human_RBP_ID_24197843,Human_RBP_ID_27353099,Human_RBP_ID_27568920 RMVar_hsa_circ_40243,RMVar_hsa_circ_29759,RMVar_hsa_circ_332101,RMVar_hsa_circ_249251,RMVar_hsa_circ_297094 115084 RMVar_ID_115084 Human_SNP_ID_869987605 m1A Human chr7 + 72925661 72925661 72925661 CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC CCGGCGCCGCGCTCCCCACCGCCGCGCTCCCCCCCGCCGCGCTCCCCCCCGCCCTCCCCGCCGAC A C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr7:72925577..72925678 26863410 MeRIP-seq:(Medium) rs1389469051 Functional Loss SNV TCGA 33..33 33 CESC 1 - RMVar_hsa_circ_312976 115085 RMVar_ID_115085 Human_SNP_ID_870013709 m1A Human chr7 + 33062736 33062735 33062736 ATGGACGGGGCCCTCATGCGCGTCCAAGCAGGAAAAAAACAGGCAGCTCGCGTAGACTGCGAGTC ATGGACGGGGCCCTCATGCGCGTCCAAGCAGG_AAAAAACAGGCAGCTCGCGTAGACTGCGAGTC GA G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:33062646..33062747 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 115086 RMVar_ID_115086 Human_SNP_ID_870036410 m1A Human chr7 - 140472013 140472013 140472013 TTTTAATCCAGTTTTGTGGTCTTTCGTCTCACAGGTATTTTATGCATGGGGTTTGTAAGGAAGGA TTTTAATCCAGTTTTGTGGTCTTTCGTCTCACGGGTATTTTATGCATGGGGTTTGTAAGGAAGGA T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr7:140471976..140472067;chr7:140471967..140472063 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_7706025,Human_RBP_ID_22686015,Human_RBP_ID_24196231 RMVar_hsa_circ_295560 115087 RMVar_ID_115087 Human_SNP_ID_870063322 m1A Human chr7 - 98192371 98192371 98192371 GGGCAAATCTTCCGATTTGTCCACATCATTAAATATATTGTTGAAAGGGCTCTCGGGGCCACTGG GGGCAAATCTTCCGATTTGTCCACATCATTAACTATATTGTTGAAAGGGCTCTCGGGGCCACTGG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:98192326..98192375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 115088 RMVar_ID_115088 Human_SNP_ID_870084503 m1A Human chr7 - 28180577 28180577 28180577 GCCGACACCAGGGGGGCTCTCGATGTAGCACCATGACAGGCATCGCCGCCGCCTCCTTCTTCTCC GCCGACACCAGGGGGGCTCTCGATGTAGCACCCTGACAGGCATCGCCGCCGCCTCCTTCTTCTCC T G JAZF1 Ensembl:ENSG00000153814 Protein coding start codon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr7:28180474..28180737;chr7:28180401..28185701;chr7:28180526..28180700 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus Human_RBP_ID_4938505,Human_RBP_ID_18881419 115089 RMVar_ID_115089 Human_SNP_ID_870093257 m1A Human chr7 + 97117806 97117806 97117806 GCAGCTGCACCGTGTTCTGCCCCCGGACCTCAAATCCCTGGGCGACCAGTACGTGAAAGACGAAT GCAGCTGCACCGTGTTCTGCCCCCGGACCTCAGATCCCTGGGCGACCAGTACGTGAAAGACGAAT A G SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:97117726..97117850 26863410 MeRIP-seq:(Medium) rs775543999 Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 2 ovary Human_RBP_ID_690573,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_17314661,Human_RBP_ID_18426052,Human_RBP_ID_24233133,Human_RBP_ID_27534217 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 115090 RMVar_ID_115090 Human_SNP_ID_870093260 m1A Human chr7 + 97117806 97117806 97117806 GCAGCTGCACCGTGTTCTGCCCCCGGACCTCAAATCCCTGGGCGACCAGTACGTGAAAGACGAAT GCAGCTGCACCGTGTTCTGCCCCCGGACCTCACATCCCTGGGCGACCAGTACGTGAAAGACGAAT A C SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:97117726..97117850 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_690573,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_17314661,Human_RBP_ID_18426052,Human_RBP_ID_24233133,Human_RBP_ID_27534217 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 115091 RMVar_ID_115091 Human_SNP_ID_870131065 m1A Human chr7 - 77618536 77618536 77618536 TACCTGCGGGTCCTTGGTGGTTTTGGAGGAGGAGAATCTTGTTTTTCAGGCTCTATGGAGCTGAC TACCTGCGGGTCCTTGGTGGTTTTGGAGGAGGGGAATCTTGTTTTTCAGGCTCTATGGAGCTGAC T C APTR RNACentral:URS0000D5A265 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:77618488..77626778 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 115092 RMVar_ID_115092 Human_SNP_ID_870143301 m1A Human chr7 - 27184540 27184540 27184540 TTCGGACAGCGGCGGCGGCGGCGGCTGCCGGGAGACGGCGGCGGCAGCAGAGGAGAAAGAGCGGC TTCGGACAGCGGCGGCGGCGGCGGCTGCCGGGGGACGGCGGCGGCAGCAGAGGAGAAAGAGCGGC T C HOXA11 Ensembl:ENSG00000005073 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:27184490..27184765 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4937695 115093 RMVar_ID_115093 Human_SNP_ID_870146663 m1A Human chr7 - 596300 596300 596300 TGACACTTCTCTCTCTTGCTCCCCAAAGGTGTACGTGAACGGAGAGTGGGTGACCAACATCAGCG TGACACTTCTCTCTCTTGCTCCCCAAAGGTGTGCGTGAACGGAGAGTGGGTGACCAACATCAGCG T C PRKAR1B Ensembl:ENSG00000188191 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:551429..602569 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 5 haematopoietic and lymphoid tissue Human_RBP_ID_86134,Human_RBP_ID_954026,Human_RBP_ID_9403069,Human_RBP_ID_19019318,Human_RBP_ID_26551040 Human_Splice_Rec_836184,Human_Splice_Rec_836204,Human_Splice_Rec_836224,Human_Splice_Rec_836244,Human_Splice_Rec_836264,Human_Splice_Rec_836274,Human_Splice_Rec_836294,Human_Splice_Rec_836308 RMVar_hsa_circ_13819,RMVar_hsa_circ_109563,RMVar_hsa_circ_302771,RMVar_hsa_circ_342825,RMVar_hsa_circ_276511,RMVar_hsa_circ_243184,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_243185,RMVar_hsa_circ_337394,RMVar_hsa_circ_243189,RMVar_hsa_circ_243191,RMVar_hsa_circ_308214,RMVar_hsa_circ_327331,RMVar_hsa_circ_369998,RMVar_hsa_circ_102398,RMVar_hsa_circ_243190,RMVar_hsa_circ_243188 115094 RMVar_ID_115094 Human_SNP_ID_870166379 m1A Human chr7 + 74189868 74189868 74189868 GTCACTTCGTGTGGACATTGCAGAAGGCAGAAAACAAGATAAAGGTGGCTTTGGATTCAGAAAAG GTCACTTCGTGTGGACATTGCAGAAGGCAGAACACAAGATAAAGGTGGCTTTGGATTCAGAAAAG A C EIF4H Ensembl:ENSG00000106682 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 READ 1 - Human_Splice_Rec_875958,Human_Splice_Rec_875959,Human_Splice_Rec_875970,Human_Splice_Rec_875976,Human_Splice_Rec_875977,Human_Splice_Rec_875990,Human_Splice_Rec_875991 RMVar_hsa_circ_33912,RMVar_hsa_circ_77583,RMVar_hsa_circ_99960,RMVar_hsa_circ_245630,RMVar_hsa_circ_345791,RMVar_hsa_circ_245632,RMVar_hsa_circ_245633,RMVar_hsa_circ_374023,RMVar_hsa_circ_245634 115095 RMVar_ID_115095 Human_SNP_ID_870185653 m1A Human chr7 + 202564 202564 202564 GACATCTTCCCGTGTGCATAGAGAGGACGGGTAGCTGCTGGGTGGGATTGTACTGGGGAATGGGG GACATCTTCCCGTGTGCATAGAGAGGACGGGTGGCTGCTGGGTGGGATTGTACTGGGGAATGGGG A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:202331..202729 26863196 MeRIP-seq:(Medium) rs1387425481 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_21042 115096 RMVar_ID_115096 Human_SNP_ID_870186461 m1A Human chr7 + 45109285 45109285 45109285 AGAGAGACAAGACTCCTAGCAAGTGATTCCAAACCCTGAAGAGAAAAAGGAGAGAGAAGGGGCTA AGAGAGACAAGACTCCTAGCAAGTGATTCCAACCCCTGAAGAGAAAAAGGAGAGAGAAGGGGCTA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:45108964..45109300;chr7:45109015..45109300;chr7:45109051..45109300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115097 RMVar_ID_115097 Human_SNP_ID_870215031 m1A Human chr7 - 99439020 99439020 99439020 CCCCCTCGGTCTCCTGCAGCCTTCTCGCCTTTACCCGCCGCCGGCCCCGCCGCACACACTCCTCC CCCCCTCGGTCTCCTGCAGCCTTCTCGCCTTTCCCCGCCGCCGGCCCCGCCGCACACACTCCTCC T G PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:99438904..99439200;chr7:99438885..99439221;chr7:99438881..99439237 26863196 MeRIP-seq:(Medium) rs894310827 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 115098 RMVar_ID_115098 Human_SNP_ID_870215356 m1A Human chr7 + 2014631 2014631 2014631 TCGCTGTCGTAGGACCCCAGGATGGCCCGCATACCGTCCCGCTCCTGTGGACACAGAGGGCAGCT TCGCTGTCGTAGGACCCCAGGATGGCCCGCATGCCGTCCCGCTCCTGTGGACACAGAGGGCAGCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:2014580..2079740 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - 115099 RMVar_ID_115099 Human_SNP_ID_870221033 m1A Human chr7 - 2219414 2219414 2219414 CACTGAAGGGGAGGATCTCGGAACTGCAGTGGAGCGTGATGGACCAGGAGATGCGGGTGAAGCGC CACTGAAGGGGAGGATCTCGGAACTGCAGTGGGGCGTGATGGACCAGGAGATGCGGGTGAAGCGC T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:2218039..2220905 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_82270,Human_RBP_ID_952339,Human_RBP_ID_3971780,Human_RBP_ID_9403103,Human_RBP_ID_18171860,Human_RBP_ID_18472266,Human_RBP_ID_19019396,Human_RBP_ID_22463849,Human_RBP_ID_23080511,Human_RBP_ID_24554910,Human_RBP_ID_26355932,Human_RBP_ID_27829134 Human_Splice_Rec_837948,Human_Splice_Rec_837949,Human_Splice_Rec_837980,Human_Splice_Rec_837981,Human_Splice_Rec_838016,Human_Splice_Rec_838017,Human_Splice_Rec_838052,Human_Splice_Rec_838053,Human_Splice_Rec_838152,Human_Splice_Rec_838153,Human_Splice_Rec_838164,Human_Splice_Rec_838165,Human_Splice_Rec_838176,Human_Splice_Rec_838200,Human_Splice_Rec_838201 Human_miRNA_ID_2968213,Human_miRNA_ID_2968214,Human_miRNA_ID_2968215 RMVar_hsa_circ_122498,RMVar_hsa_circ_86588,RMVar_hsa_circ_243299,RMVar_hsa_circ_243298,RMVar_hsa_circ_37297,RMVar_hsa_circ_79209,RMVar_hsa_circ_243306,RMVar_hsa_circ_31714,RMVar_hsa_circ_9871,RMVar_hsa_circ_101973,RMVar_hsa_circ_38270,RMVar_hsa_circ_318575,RMVar_hsa_circ_343244,RMVar_hsa_circ_268090,RMVar_hsa_circ_243307,RMVar_hsa_circ_296354,RMVar_hsa_circ_309050,RMVar_hsa_circ_276152,RMVar_hsa_circ_127460,RMVar_hsa_circ_243309,RMVar_hsa_circ_243310,RMVar_hsa_circ_243311,RMVar_hsa_circ_45027,RMVar_hsa_circ_50677,RMVar_hsa_circ_109414,RMVar_hsa_circ_243312,RMVar_hsa_circ_243313 115100 RMVar_ID_115100 Human_SNP_ID_870223281 m1A Human chr7 - 130439957 130439957 130439957 GTGAACAGAATTTGAGTACAGTGTGGTCGGGGAGCAAGATGTTACGAGAAAATAGGTAGTACTCA GTGAACAGAATTTGAGTACAGTGTGGTCGGGGGGCAAGATGTTACGAGAAAATAGGTAGTACTCA T C CEP41 Ensembl:ENSG00000106477 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:130439834..130439960 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115101 RMVar_ID_115101 Human_SNP_ID_870286742 m1A Human chr7 - 106660421 106660419 106660422 GCCGCCACCCCCACCGCCGCCGCCCCCCGAGGAGAGCTGCCCGGCCAAGCCCGTGGCCCCCGGGC GCCGCCACCCCCACCGCCGCCGCCCCCCGAG___AGCTGCCCGGCCAAGCCCGTGGCCCCCGGGC TCTC T AC004917.1,CCDC71L Ensembl:ENSG00000243797,Ensembl:ENSG00000253276 lincRNA,Protein coding intron,CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:106660099..106660598 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 THCA 1 - Human_RBP_ID_22463276 115102 RMVar_ID_115102 Human_SNP_ID_870300102 m1A Human chr7 - 103344697 103344697 103344697 AGCCAAGGCGCGAGGCTCGGAGTGAGAGGTAGAGCTGGAGGGGACCCTAAGCGCCCTCCGCCCGG AGCCAAGGCGCGAGGCTCGGAGTGAGAGGTAGGGCTGGAGGGGACCCTAAGCGCCCTCCGCCCGG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:103344551..103344825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_86760,Human_RBP_ID_4956587,Human_RBP_ID_8906661,Human_RBP_ID_9311417,Human_RBP_ID_9403780,Human_RBP_ID_18472391,Human_RBP_ID_19021383,Human_RBP_ID_26356053,Human_RBP_ID_27830656 115103 RMVar_ID_115103 Human_SNP_ID_870326266 m1A Human chr7 - 102538297 102538295 102538297 GACCCTGAGAGAGATTGTTTCTTTTCTTTACTATTTTTTTTTTTTTTTTTGAGACGGAGTCTCAC GACCCTGAGAGAGATTGTTTCTTTTCTTTACT__TTTTTTTTTTTTTTTTGAGACGGAGTCTCAC AAT A POLR2J3 Ensembl:ENSG00000168255 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 33..34 33 TGCT 1 - Human_RBP_ID_671941,Human_RBP_ID_7668326 RMVar_hsa_circ_97247,RMVar_hsa_circ_91883,RMVar_hsa_circ_247345,RMVar_hsa_circ_247346 115104 RMVar_ID_115104 Human_SNP_ID_870333131 m1A Human chr7 + 127582300 127582300 127582300 CCTCCTCCAGCAGCCGATCCTGCAGCTGATGCACCTCGACCTCCAGCCTGTGCTTCTGCTTCCTC CCTCCTCCAGCAGCCGATCCTGCAGCTGATGCCCCTCGACCTCCAGCCTGTGCTTCTGCTTCCTC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:127582250..127582315 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115105 RMVar_ID_115105 Human_SNP_ID_870333958 m1A Human chr7 + 13935768 13935768 13935768 GTATGGACTGCGATGGAGGGAGGTGAGCTGGGAAGGCCCGGTCAGGTTTCGGTGTATGAGTTGAG GTATGGACTGCGATGGAGGGAGGTGAGCTGGGGAGGCCCGGTCAGGTTTCGGTGTATGAGTTGAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:13935725..13935824 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue 115106 RMVar_ID_115106 Human_SNP_ID_870341391 m1A Human chr7 + 128653327 128653327 128653327 GCCCAGCTCCCAACCGCCTTTCTAGGCCCCGAACTTTCTCCAGCCAAGCTCTGAGGGCCCACCTC GCCCAGCTCCCAACCGCCTTTCTAGGCCCCGAGCTTTCTCCAGCCAAGCTCTGAGGGCCCACCTC A G LINC01000,LINC01000:2 RNACentral:URS00008C0C4E,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:128653276..128653375 26863196 MeRIP-seq:(Medium) rs1255506639 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_27528277 115107 RMVar_ID_115107 Human_SNP_ID_870342650 m1A Human chr7 - 36440227 36440227 36440227 TCCCTCCTTCCATCCGTCCTTTCAATGCTGGCACTCCTCCAGTGAGTTGGCTCTGCTTCCCTCAC TCCCTCCTTCCATCCGTCCTTTCAATGCTGGCTCTCCTCCAGTGAGTTGGCTCTGCTTCCCTCAC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:36440176..36440247 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115108 RMVar_ID_115108 Human_SNP_ID_870381808 m1A Human chr7 + 143286731 143286731 143286731 CTCCTGATCTGCAGAGCTTGGCGGCAGTCCCCACATTAGAGCCTCTGACTCCACCCCCTGCCTAT CTCCTGATCTGCAGAGCTTGGCGGCAGTCCCCTCATTAGAGCCTCTGACTCCACCCCCTGCCTAT A T TMEM139 Ensembl:ENSG00000178826 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:143286727..143286892 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 115109 RMVar_ID_115109 Human_SNP_ID_870389868 m1A Human chr7 - 4785577 4785577 4785577 GGGCCTTCAGGCAGGAGAGACTTCGGTACAGGAAGGACGGGTCCTGCCGGCACAGCACGTCCAGC GGGCCTTCAGGCAGGAGAGACTTCGGTACAGGGAGGACGGGTCCTGCCGGCACAGCACGTCCAGC T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:4785468..4785576 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115110 RMVar_ID_115110 Human_SNP_ID_870398438 m1A Human chr7 - 100209866 100209866 100209866 CAGCTATCTTCACTCTCTGCCTTCCCCATCTCAGATACTGTCAACTCCATCCTTCTGTCAGGCCA CAGCTATCTTCACTCTCTGCCTTCCCCATCTCGGATACTGTCAACTCCATCCTTCTGTCAGGCCA T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100209839..100209975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 115111 RMVar_ID_115111 Human_SNP_ID_870403625 m1A Human chr7 - 38273629 38273629 38273629 GCTTCTCAGGTGGTGGGCAAGAGTTGGGCAAAAAAATCAAGGTATTTGGTCCCGGAACAAAGCTT GCTTCTCAGGTGGTGGGCAAGAGTTGGGCAAACAAATCAAGGTATTTGGTCCCGGAACAAAGCTT T G TRGJP Ensembl:ENSG00000211691 Other CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:38273556..38273641 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - 115112 RMVar_ID_115112 Human_SNP_ID_870417057 m1A Human chr7 + 35832851 35832851 35832851 TATGTGGGATTTGCCAATCTCCCAAATCAAGTATACAGAAAATCGGTGAAGAGAGGTTTTGAATT TATGTGGGATTTGCCAATCTCCCAAATCAAGTGTACAGAAAATCGGTGAAGAGAGGTTTTGAATT A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:35832743..35832925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_683648,Human_RBP_ID_4963104,Human_RBP_ID_9210628,Human_RBP_ID_9403298,Human_RBP_ID_24213576 Human_Splice_Rec_857466,Human_Splice_Rec_857467,Human_Splice_Rec_857470,Human_Splice_Rec_857471,Human_Splice_Rec_857493,Human_Splice_Rec_857540,Human_Splice_Rec_857541,Human_Splice_Rec_857548,Human_Splice_Rec_857549,Human_Splice_Rec_857558,Human_Splice_Rec_857559,Human_Splice_Rec_857568,Human_Splice_Rec_857570,Human_Splice_Rec_857571,Human_Splice_Rec_857582,Human_Splice_Rec_857583,Human_Splice_Rec_857592,Human_Splice_Rec_857593,Human_Splice_Rec_857618,Human_Splice_Rec_857619,Human_Splice_Rec_857624,Human_Splice_Rec_857625,Human_Splice_Rec_857647 RMVar_hsa_circ_41185,RMVar_hsa_circ_244625,RMVar_hsa_circ_244624,RMVar_hsa_circ_361759,RMVar_hsa_circ_295838,RMVar_hsa_circ_46175,RMVar_hsa_circ_269341 115113 RMVar_ID_115113 Human_SNP_ID_870419203 m1A Human chr7 - 38761181 38761181 38761181 GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGACAAGGAAGGAAAGACAAGGAAAGGGAAACAGA GAAAAGGAAGGGAGGGAGGGAAGAAAGGAAGGTCAAGGAAGGAAAGACAAGGAAAGGGAAACAGA T A VPS41 Ensembl:ENSG00000006715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:38761132..38761234 26863196 MeRIP-seq:(Medium) rs2286084 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_12613,GWAS_ID_12614,GWAS_ID_12615,GWAS_ID_12616,GWAS_ID_12617,GWAS_ID_12618,GWAS_ID_12619,GWAS_ID_12620,GWAS_ID_12621,GWAS_ID_12622,GWAS_ID_12623,GWAS_ID_12624 RMVar_hsa_circ_43146,RMVar_hsa_circ_68611,RMVar_hsa_circ_244709,RMVar_hsa_circ_111681,RMVar_hsa_circ_343704,RMVar_hsa_circ_363123,RMVar_hsa_circ_33766,RMVar_hsa_circ_33247,RMVar_hsa_circ_84413,RMVar_hsa_circ_50262,RMVar_hsa_circ_76428,RMVar_hsa_circ_244710,RMVar_hsa_circ_244711 115114 RMVar_ID_115114 Human_SNP_ID_870432777 m1A Human chr7 + 1539199 1539199 1539199 TCTGTCCTGGTGACCGTGCCCGGGTTATGACGACTAATCCCAAACCGAATAAGGCATTAAAGGTA TCTGTCCTGGTGACCGTGCCCGGGTTATGACGGCTAATCCCAAACCGAATAAGGCATTAAAGGTA A G MAFK Ensembl:ENSG00000198517 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:1539111..1539250;chr7:1539126..1540285;chr7:1539126..1539250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_87584,Human_RBP_ID_3076507 Human_Splice_Rec_837756,Human_Splice_Rec_837757,Human_Splice_Rec_837760,Human_Splice_Rec_837761,Human_Splice_Rec_837766,Human_Splice_Rec_837767 RMVar_hsa_circ_22871 115115 RMVar_ID_115115 Human_SNP_ID_870441762 m1A Human chr7 - 111562382 111562382 111562382 GCTGGCAGGGGTCGGCGGGCGCGTAGCCGCCGACCCTTGGTGGTCTCTTGGGCTGGGGACCCTTC GCTGGCAGGGGTCGGCGGGCGCGTAGCCGCCGGCCCTTGGTGGTCTCTTGGGCTGGGGACCCTTC T C IMMP2L Ensembl:ENSG00000184903 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:111562377..111562473 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_7677854,Human_RBP_ID_9337958,Human_RBP_ID_9439364,Human_RBP_ID_18426637,Human_RBP_ID_18960342,Human_RBP_ID_22686499,Human_RBP_ID_26793629,Human_RBP_ID_27842947 115116 RMVar_ID_115116 Human_SNP_ID_870449372 m1A Human chr7 - 75915211 75915211 75915211 CAAACCCCGAGTCTTGGGGCCCGACCTCACCCACCCCGCCGTCGCCGCGAAAGATAGCACTCACC CAAACCCCGAGTCTTGGGGCCCGACCTCACCCCCCCCGCCGTCGCCGCGAAAGATAGCACTCACC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:75915206..75915390 26863196 MeRIP-seq:(Medium) rs1554547903 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115117 RMVar_ID_115117 Human_SNP_ID_870453844 m1A Human chr7 + 128092097 128092097 128092097 GATCGGGTTTGGCCCCCAGCCCCGCTCACGCCAGTCCCTCTTCCTCTGCCGGGAGGGTGTTTTCA GATCGGGTTTGGCCCCCAGCCCCGCTCACGCCGGTCCCTCTTCCTCTGCCGGGAGGGTGTTTTCA A G SND1 Ensembl:ENSG00000197157 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:128092048..128092180 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_674498,Human_RBP_ID_4923477,Human_RBP_ID_17427121,Human_RBP_ID_17665113,Human_RBP_ID_22463317,Human_RBP_ID_27351538 Human_miRNA_ID_2351554,Human_miRNA_ID_3047101 RMVar_hsa_circ_76934,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_81641,RMVar_hsa_circ_248208 115118 RMVar_ID_115118 Human_SNP_ID_870461958 m1A Human chr7 + 202348 202348 202348 ATATCTTCCAGTGTGCATAGAGAGAATGGGTGACTGCTGGGTGAGATTGCACTGGGGAATGGGGC ATATCTTCCAGTGTGCATAGAGAGAATGGGTGGCTGCTGGGTGAGATTGCACTGGGGAATGGGGC A G FAM20C Ensembl:ENSG00000177706 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:202344..202710 26863196 MeRIP-seq:(Medium) rs866682185 Functional Loss SNV ICGC 33..33 33 LUSC 2 - RMVar_hsa_circ_21042 115119 RMVar_ID_115119 Human_SNP_ID_870473402 m1A Human chr7 + 102248533 102248533 102248533 GCGGCCGGGCGGCGCCCAGCTCGGAGGGCGACAGCTGCGACGGCGTGGAGGCCACTGAGGGCCCA GCGGCCGGGCGGCGCCCAGCTCGGAGGGCGACTGCTGCGACGGCGTGGAGGCCACTGAGGGCCCA A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:102248483..102248694 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 15 liver Human_RBP_ID_9311414 RMVar_hsa_circ_85687,RMVar_hsa_circ_247267,RMVar_hsa_circ_267024,RMVar_hsa_circ_264945,RMVar_hsa_circ_266127,RMVar_hsa_circ_87521,RMVar_hsa_circ_247291 115120 RMVar_ID_115120 Human_SNP_ID_870535123 m1A Human chr7 - 138861241 138861232 138861242 GCCAGCACCGCAGGTGTAGGCCCCGGAGTCCCACCCGGCCTGCCCGCAAACAGCACCCCTTCCCA GCCAGCACCGCAGGTGTAGGCCCCGGAGTCC__________GCCCGCAAACAGCACCCCTTCCCA CAGGCCGGGTG C KIAA1549 Ensembl:ENSG00000122778 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:138861192..138861456 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..41 33 SKCA 1 - RMVar_hsa_circ_61384,RMVar_hsa_circ_315411,RMVar_hsa_circ_248913,RMVar_hsa_circ_305476,RMVar_hsa_circ_326280 115121 RMVar_ID_115121 Human_SNP_ID_870541451 m1A Human chr7 + 155680841 155680841 155680841 AGAAGACCAAATAGAATATGTGGAAGAGCCAGAGGAGGAGCAGCTTTACACTGATGAAGTGTTAG AGAAGACCAAATAGAATATGTGGAAGAGCCAGGGGAGGAGCAGCTTTACACTGATGAAGTGTTAG A G RBM33 Ensembl:ENSG00000184863 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:155680724..155680854;chr7:155680713..155680864 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_85618,Human_RBP_ID_7715228,Human_RBP_ID_8238174,Human_RBP_ID_9404114,Human_RBP_ID_16082162,Human_RBP_ID_18414254,Human_RBP_ID_24549059,Human_RBP_ID_26357393,Human_RBP_ID_27830056 Human_Splice_Rec_942013,Human_Splice_Rec_942023,Human_Splice_Rec_942057,Human_Splice_Rec_942065,Human_Splice_Rec_942083 Human_miRNA_ID_2406187,Human_miRNA_ID_2406188,Human_miRNA_ID_2406189,Human_miRNA_ID_2409182,Human_miRNA_ID_2409183,Human_miRNA_ID_2409184,Human_miRNA_ID_2412167,Human_miRNA_ID_2412168,Human_miRNA_ID_2412169,Human_miRNA_ID_2415142,Human_miRNA_ID_2415143,Human_miRNA_ID_2415144,Human_miRNA_ID_2623655,Human_miRNA_ID_2623656,Human_miRNA_ID_2623657,Human_miRNA_ID_3105094,Human_miRNA_ID_3105095,Human_miRNA_ID_3105096 RMVar_hsa_circ_72846,RMVar_hsa_circ_249671,RMVar_hsa_circ_43949,RMVar_hsa_circ_287427,RMVar_hsa_circ_249669,RMVar_hsa_circ_306816,RMVar_hsa_circ_301455,RMVar_hsa_circ_273953,RMVar_hsa_circ_271746,RMVar_hsa_circ_249673,RMVar_hsa_circ_249674,RMVar_hsa_circ_249672,RMVar_hsa_circ_114504,RMVar_hsa_circ_124662,RMVar_hsa_circ_282392,RMVar_hsa_circ_318458,RMVar_hsa_circ_249670,RMVar_hsa_circ_316104,RMVar_hsa_circ_275671,RMVar_hsa_circ_120729,RMVar_hsa_circ_89341,RMVar_hsa_circ_108904,RMVar_hsa_circ_87877,RMVar_hsa_circ_249686,RMVar_hsa_circ_121261,RMVar_hsa_circ_249679,RMVar_hsa_circ_249681,RMVar_hsa_circ_249683,RMVar_hsa_circ_249684,RMVar_hsa_circ_249682,RMVar_hsa_circ_249680,RMVar_hsa_circ_249678,RMVar_hsa_circ_295604,RMVar_hsa_circ_369595,RMVar_hsa_circ_127344,RMVar_hsa_circ_56717,RMVar_hsa_circ_65593,RMVar_hsa_circ_249687,RMVar_hsa_circ_249688,RMVar_hsa_circ_249690,RMVar_hsa_circ_71105,RMVar_hsa_circ_249685,RMVar_hsa_circ_374923,RMVar_hsa_circ_249689 115122 RMVar_ID_115122 Human_SNP_ID_870547182 m1A Human chr7 + 55978201 55978201 55978201 CTAAAATCCTTATTTGTCCGGAAAGTTGATCCAAGAAAAGATGCCCACTCCAATCTCCTAGCCAA CTAAAATCCTTATTTGTCCGGAAAGTTGATCCGAGAAAAGATGCCCACTCCAATCTCCTAGCCAA A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:55978151..55978200 26863196 MeRIP-seq:(Medium) rs768965920 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 2 head and neck Human_RBP_ID_2044304,Human_RBP_ID_4945115,Human_RBP_ID_18883989,Human_RBP_ID_24219685 Human_Splice_Rec_868728,Human_Splice_Rec_868729,Human_Splice_Rec_868740,Human_Splice_Rec_868741,Human_Splice_Rec_868754,Human_Splice_Rec_868755,Human_Splice_Rec_868772,Human_Splice_Rec_868773,Human_Splice_Rec_868776,Human_Splice_Rec_868777,Human_Splice_Rec_868788,Human_Splice_Rec_868789,Human_Splice_Rec_868802,Human_Splice_Rec_868803,Human_Splice_Rec_868810,Human_Splice_Rec_868811 RMVar_hsa_circ_68642,RMVar_hsa_circ_123218,RMVar_hsa_circ_336552,RMVar_hsa_circ_362054,RMVar_hsa_circ_245197,RMVar_hsa_circ_346772,RMVar_hsa_circ_305234,RMVar_hsa_circ_245199,RMVar_hsa_circ_245200,RMVar_hsa_circ_245198 115123 RMVar_ID_115123 Human_SNP_ID_870565015 m1A Human chr7 - 66921348 66921348 66921348 TCGTGGCGGCGCGTGGCGGGCCCGAGGCCGCTAGGCACCATCTTCTCCCCGCGCCGGGGGCAGCG TCGTGGCGGCGCGTGGCGGGCCCGAGGCCGCTCGGCACCATCTTCTCCCCGCGCCGGGGGCAGCG T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:66921248..66921517 26863196 MeRIP-seq:(Medium) rs2293350 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115124 RMVar_ID_115124 Human_SNP_ID_870580653 m1A Human chr7 + 134935678 134935678 134935678 TTCTTTTACTTGTGTGACCTTACCATTCTTGAAAATAAAAAGGGAGAAGAGAAGGGAACTAAAGT TTCTTTTACTTGTGTGACCTTACCATTCTTGACAATAAAAAGGGAGAAGAGAAGGGAACTAAAGT A C CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:134935676..134935775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_23081107 Human_Splice_Rec_925455,Human_Splice_Rec_925495,Human_Splice_Rec_925615,Human_Splice_Rec_925685 RMVar_hsa_circ_89029,RMVar_hsa_circ_61892,RMVar_hsa_circ_248678 115125 RMVar_ID_115125 Human_SNP_ID_870584037 m1A Human chr7 - 158871261 158871261 158871261 TGGACTTCGGCCACCCTGTCTCTGCTCCTGGCATCCTGGTCGGGATCCCTGCACCTCGGCTCCTT TGGACTTCGGCCACCCTGTCTCTGCTCCTGGCTTCCTGGTCGGGATCCCTGCACCTCGGCTCCTT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:158871229..158871575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 HNSC 1 - 115126 RMVar_ID_115126 Human_SNP_ID_870588315 m1A Human chr7 - 868626 868626 868626 AGCACTGTCCCCCCATCCGACCAACACCACAGAGAACCAGCACTGCCCCCCCATCCGACCAACAC AGCACTGTCCCCCCATCCGACCAACACCACAGGGAACCAGCACTGCCCCCCCATCCGACCAACAC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:868397..868684;chr7:868550..868683 26863196 MeRIP-seq:(Medium) rs1207988303 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115127 RMVar_ID_115127 Human_SNP_ID_870599339 m1A Human chr7 - 73521912 73521912 73521912 CCGCCGCCGCGATGGCGCCGCTCCTGGGCCGCAAGCCCTTCCCGCTGGTGAAGCCGTTGCCCGGA CCGCCGCCGCGATGGCGCCGCTCCTGGGCCGCGAGCCCTTCCCGCTGGTGAAGCCGTTGCCCGGA T C BAZ1B Ensembl:ENSG00000009954 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:73521865..73522275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_4956402,Human_RBP_ID_8914423,Human_RBP_ID_9311308,Human_RBP_ID_18885498 Human_Splice_Rec_873557,Human_Splice_Rec_873595 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 115128 RMVar_ID_115128 Human_SNP_ID_870611220 m1A Human chr7 + 128654179 128654179 128654179 TCAGCTCCTGCCCAGCTCCCAGAGGCCCTGGTAGGCCCACAACTTCCCTAAGCCAAGCTCCCCAG TCAGCTCCTGCCCAGCTCCCAGAGGCCCTGGTCGGCCCACAACTTCCCTAAGCCAAGCTCCCCAG A C AC018638.5 Ensembl:ENSG00000243679 Pseudogene exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr7:128654080..128654244 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_176204,Human_RBP_ID_254045,Human_RBP_ID_795191,Human_RBP_ID_955503,Human_RBP_ID_1397342,Human_RBP_ID_1691220,Human_RBP_ID_3868345,Human_RBP_ID_8220525,Human_RBP_ID_8272481,Human_RBP_ID_8915474,Human_RBP_ID_9217217,Human_RBP_ID_10370395,Human_RBP_ID_10485691,Human_RBP_ID_17093824,Human_RBP_ID_17316564,Human_RBP_ID_17429627,Human_RBP_ID_17543802,Human_RBP_ID_17577242,Human_RBP_ID_18172390,Human_RBP_ID_18541071,Human_RBP_ID_18960725,Human_RBP_ID_19139597,Human_RBP_ID_21960756,Human_RBP_ID_21994384,Human_RBP_ID_22111204,Human_RBP_ID_22372426,Human_RBP_ID_27528278 Human_miRNA_ID_1869407 115129 RMVar_ID_115129 Human_SNP_ID_870637221 m1A Human chr7 - 152435749 152435749 152435749 GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCAGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG GTCGGAGGAGGACAAGAGCGTGGAGCAGCCGCCGCCGCCGCCACCACCCCCCGAGGAGCCTGGAG T G KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:152435703..152435783 26863196 MeRIP-seq:(Medium) rs866392536 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_252986,Human_RBP_ID_842694,Human_RBP_ID_19021665,Human_RBP_ID_23080479 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 115130 RMVar_ID_115130 Human_SNP_ID_870640850 m1A Human chr7 - 105112985 105112985 105112985 GCACTCGAAGGAAAAAGTGGAGGTCCTTGATGAGGTGGGTGGTGTAAGGCTTGAGCTGATGTGGT GCACTCGAAGGAAAAAGTGGAGGTCCTTGATGGGGTGGGTGGTGTAAGGCTTGAGCTGATGTGGT T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105112934..105113047 26863196 MeRIP-seq:(Medium) rs770445089 Functional Loss SNV COSMIC 33..33 33 ovary mucinous_carcinoma 2 ovary Human_RBP_ID_7670712 115131 RMVar_ID_115131 Human_SNP_ID_870685466 m1A Human chr7 - 100805594 100805594 100805594 GCTCATGCTGGACTGTTGGCAGAAAGACCGGAATGCCCGGCCCCGCTTCCCCCAGGTGGTCAGCG GCTCATGCTGGACTGTTGGCAGAAAGACCGGAGTGCCCGGCCCCGCTTCCCCCAGGTGGTCAGCG T C EPHB4 Ensembl:ENSG00000196411 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100805543..100805714 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_253856,Human_RBP_ID_9311919,Human_RBP_ID_18196019 Human_Splice_Rec_901081,Human_Splice_Rec_901105,Human_Splice_Rec_901137,Human_Splice_Rec_901167 Human_miRNA_ID_2668769,Human_miRNA_ID_3065713 RMVar_hsa_circ_80807,RMVar_hsa_circ_88378,RMVar_hsa_circ_101224,RMVar_hsa_circ_247162,RMVar_hsa_circ_247163,RMVar_hsa_circ_247164 115132 RMVar_ID_115132 Human_SNP_ID_870690109 m1A Human chr7 - 100430861 100430861 100430861 GGGGTGAGAGGGGCTGTGGGCGGCACGGGGTGACTCTCACTCCCTCCGGCTGCCTGCTGCTGCTG GGGGTGAGAGGGGCTGTGGGCGGCACGGGGTGGCTCTCACTCCCTCCGGCTGCCTGCTGCTGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100430811..100431051 26863196 MeRIP-seq:(Medium) rs6962151 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,ESCA 3 head and neck 115133 RMVar_ID_115133 Human_SNP_ID_870718744 m1A Human chr7 - 92096949 92096949 92096949 GAGGGCAAGGGTGGCCGAGACTGTCCAGTACCATCACTGCTCTGCAGCTGTGCGTGCAATTCCCG GAGGGCAAGGGTGGCCGAGACTGTCCAGTACCGTCACTGCTCTGCAGCTGTGCGTGCAATTCCCG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:92096898..92097006 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_21541105 115134 RMVar_ID_115134 Human_SNP_ID_870721327 m1A Human chr7 + 27096253 27096250 27096253 ACTGCAAAGGCCGATTTGGAGTGCTGGAGCGAAGAAGAGCAAAAGCTGCGTTCTGCGCGCGCCCG ACTGCAAAGGCCGATTTGGAGTGCTGGAGC___GAAGAGCAAAAGCTGCGTTCTGCGCGCGCCCG CGAA C HOTAIRM1 Ensembl:ENSG00000233429 lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:27096123..27096383 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 ORCA 1 - Human_RBP_ID_1685608,Human_RBP_ID_5452286,Human_RBP_ID_5625855,Human_RBP_ID_8272936 Human_Splice_Rec_851654 Human_miRNA_ID_3170853 115135 RMVar_ID_115135 Human_SNP_ID_870728148 m1A Human chr7 + 105143206 105143206 105143206 TGGAAGGTGCAGCTGAGGTGATGTTTTCTTCTATTATTTTCCTTTCAGCTTCTCGCTCCAATTCT TGGAAGGTGCAGCTGAGGTGATGTTTTCTTCTGTTATTTTCCTTTCAGCTTCTCGCTCCAATTCT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:105143156..105143283 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 left_upper_lobe adenocarcinoma,lung adenocarcinoma,LUAD 5 lung 115136 RMVar_ID_115136 Human_SNP_ID_870728175 m1A Human chr7 - 6330955 6330955 6330955 ACAAAGTGAGGCATTATCACTGGAAATGAGAAAGGATCCGAGCGGGGCTGGCCTCTGGCTTCACA ACAAAGTGAGGCATTATCACTGGAAATGAGAACGGATCCGAGCGGGGCTGGCCTCTGGCTTCACA T G FAM220A,AC009412.1 Ensembl:ENSG00000178397,Ensembl:ENSG00000286075 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:6330904..6331204 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 115137 RMVar_ID_115137 Human_SNP_ID_870730270 m1A Human chr7 - 100872730 100872730 100872730 GTGCTGGGGGCCCCTGACCTCGCACTTGTAACAGCCAATGTGAAAACTTCGATCCAGAGCAACAA GTGCTGGGGGCCCCTGACCTCGCACTTGTAACGGCCAATGTGAAAACTTCGATCCAGAGCAACAA T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:100872680..100872795 26863196 MeRIP-seq:(Medium) rs771447927 Functional Loss SNV ICGC 33..33 33 STAD 1 - 115138 RMVar_ID_115138 Human_SNP_ID_870757075 m1A Human chr7 - 711477 711477 711477 CGCCATGGCCTCCCCGCCCGCCTGCCCCTCGGAGGAGGACGAGAGCCTGAAGGGCTGTGAGCTGT CGCCATGGCCTCCCCGCCCGCCTGCCCCTCGGCGGAGGACGAGAGCCTGAAGGGCTGTGAGCTGT T G PRKAR1B Ensembl:ENSG00000188191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:711426..712430 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_4956098,Human_RBP_ID_26356108 Human_Splice_Rec_836174,Human_Splice_Rec_836194,Human_Splice_Rec_836214,Human_Splice_Rec_836234,Human_Splice_Rec_836254,Human_Splice_Rec_836284,Human_Splice_Rec_836310,Human_Splice_Rec_836318,Human_Splice_Rec_836322 RMVar_hsa_circ_109563,RMVar_hsa_circ_276511,RMVar_hsa_circ_243186,RMVar_hsa_circ_243187,RMVar_hsa_circ_337394,RMVar_hsa_circ_85211,RMVar_hsa_circ_243191,RMVar_hsa_circ_327331,RMVar_hsa_circ_243192,RMVar_hsa_circ_349783,RMVar_hsa_circ_271059,RMVar_hsa_circ_243194,RMVar_hsa_circ_243198,RMVar_hsa_circ_243193,RMVar_hsa_circ_339161,RMVar_hsa_circ_243197 115139 RMVar_ID_115139 Human_SNP_ID_870759334 m1A Human chr7 + 97117764 97117764 97117764 GCGGCACGTTTCTCGAGTCCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC GCGGCACGTTTCTCGAGTCCGGGCATTGTACATGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC A T SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:97117701..97117866 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 8 brain Human_RBP_ID_1689856,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_16256731,Human_RBP_ID_17314661,Human_RBP_ID_17426998,Human_RBP_ID_18426052 Human_miRNA_ID_1428735,Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 115140 RMVar_ID_115140 Human_SNP_ID_870759379 m1A Human chr7 + 97117764 97117764 97117764 GCGGCACGTTTCTCGAGTCCGGGCATTGTACAAGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC GCGGCACGTTTCTCGAGTCCGGGCATTGTACACGCGCGTCTTGCAGCTGCACCGTGTTCTGCCCC A C SDHAF3 Ensembl:ENSG00000196636 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:97117701..97117866 26863196 MeRIP-seq:(Medium) rs754390024 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_1689856,Human_RBP_ID_4956473,Human_RBP_ID_5328496,Human_RBP_ID_9337231,Human_RBP_ID_16256731,Human_RBP_ID_17314661,Human_RBP_ID_17426998,Human_RBP_ID_18426052 Human_miRNA_ID_1428735,Human_miRNA_ID_2012338,Human_miRNA_ID_2758712 RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 115141 RMVar_ID_115141 Human_SNP_ID_870766104 m1A Human chr7 + 94665640 94665640 94665640 CCACAGTACCCGCCGCCACAGCCGCCGCCTCCACCACCACCACCGCCGCCGCCTCCATCTTACAG CCACAGTACCCGCCGCCACAGCCGCCGCCTCCTCCACCACCACCGCCGCCGCCTCCATCTTACAG A T PEG10 Ensembl:ENSG00000242265 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:94665589..94665693 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,COCA,large_intestine adenocarcinoma 13 prostate,large intestine Human_RBP_ID_175677,Human_RBP_ID_7772139,Human_RBP_ID_17543356,Human_RBP_ID_27534120 RMVar_hsa_circ_76328,RMVar_hsa_circ_246674,RMVar_hsa_circ_111282,RMVar_hsa_circ_246677 115142 RMVar_ID_115142 Human_SNP_ID_870766474 m1A Human chr7 - 30594995 30594995 30594995 GGGACCGGCGGAGCAGGAGCGAGGGTCGGGCTAAGAGCCGGGGCGGCAGCAGCAGCAGCAGAGCG GGGACCGGCGGAGCAGGAGCGAGGGTCGGGCTCAGAGCCGGGGCGGCAGCAGCAGCAGCAGAGCG T G GARS1-DT Ensembl:ENSG00000196295 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:30594851..30595855 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115143 RMVar_ID_115143 Human_SNP_ID_870767435 m1A Human chr7 + 74376682 74376679 74376682 AGTTCCTCAAGGAGCAGATCTCGCTGGCCGAGAAGAAGATGTTGGACTACGAGCGGCTGCAGCGG AGTTCCTCAAGGAGCAGATCTCGCTGGCCG___AGAAGATGTTGGACTACGAGCGGCTGCAGCGG GAGA G CLIP2 Ensembl:ENSG00000106665 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74376632..74376749 26863196 MeRIP-seq:(Medium) rs1273300405 Functional Loss DEL ICGC 31..33 33 STAD 1 - Human_RBP_ID_9403479 RMVar_hsa_circ_107546,RMVar_hsa_circ_2528,RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_245669,RMVar_hsa_circ_372852,RMVar_hsa_circ_83371,RMVar_hsa_circ_245672,RMVar_hsa_circ_103650,RMVar_hsa_circ_245670,RMVar_hsa_circ_245679,RMVar_hsa_circ_372481,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245685,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_8106,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245693,RMVar_hsa_circ_103611,RMVar_hsa_circ_282092,RMVar_hsa_circ_313787,RMVar_hsa_circ_245694,RMVar_hsa_circ_245692 115144 RMVar_ID_115144 Human_SNP_ID_870820745 m1A Human chr7 + 74499400 74499400 74499400 CTGAGGGTTCAAAAGTGTGCAAGGAAGGGAGGAAGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG CTGAGGGTTCAAAAGTGTGCAAGGAAGGGAGGGAGGGAAGGAAGGAAGGAAGGAAGAGAAGGGAG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:74499396..74499588 26863196 MeRIP-seq:(Medium) rs10224601 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3099811,Human_RBP_ID_24226026 115145 RMVar_ID_115145 Human_SNP_ID_870837450 m1A Human chr7 - 47474614 47474614 47474614 TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGAGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT TGGTGTGTGTTGTGTGTGAAGTGTTGTGTGTGTGGTGTTTTGTGTGTGAGGTGTGTCTTGTGTGT T A TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:47474580..47475128 26863196 MeRIP-seq:(Medium) rs1308209977 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8951800 RMVar_hsa_circ_37444,RMVar_hsa_circ_351428,RMVar_hsa_circ_63411,RMVar_hsa_circ_341871,RMVar_hsa_circ_57257,RMVar_hsa_circ_57472,RMVar_hsa_circ_349290,RMVar_hsa_circ_124921,RMVar_hsa_circ_245087,RMVar_hsa_circ_245088,RMVar_hsa_circ_63766,RMVar_hsa_circ_84433,RMVar_hsa_circ_282851,RMVar_hsa_circ_54084,RMVar_hsa_circ_373210,RMVar_hsa_circ_106174,RMVar_hsa_circ_245096,RMVar_hsa_circ_245098,RMVar_hsa_circ_245099,RMVar_hsa_circ_245097,RMVar_hsa_circ_127348,RMVar_hsa_circ_245100,RMVar_hsa_circ_121399,RMVar_hsa_circ_365251,RMVar_hsa_circ_245102,RMVar_hsa_circ_245103 115146 RMVar_ID_115146 Human_SNP_ID_870842152 m1A Human chr7 + 6702384 6702382 6702384 CGCACACACACCAGATTCATCTCCCAAACTCCACACACACACACACAACCAGATTCGTCTCCCAA CGCACACACACCAGATTCATCTCCCAAACTC__CACACACACACACAACCAGATTCGTCTCCCAA CCA C AC073343.2 Ensembl:ENSG00000228010 lincRNA intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated chr7:6702347..6702499;chr7:6702344..6702559 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 ESCA 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115147 RMVar_ID_115147 Human_SNP_ID_870843894 m1A Human chr7 - 137912897 137912897 137912897 GGAATATGGCGAGAGAGCTGGGATGAGTTTGTACCACAGATGTTGTAGCTGGCTTTATGAAATAG GGAATATGGCGAGAGAGCTGGGATGAGTTTGTGCCACAGATGTTGTAGCTGGCTTTATGAAATAG T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:137912894..137912973 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_8659439,Human_RBP_ID_16032493,Human_RBP_ID_19135496 RMVar_hsa_circ_26117,RMVar_hsa_circ_100568,RMVar_hsa_circ_248857,RMVar_hsa_circ_84368,RMVar_hsa_circ_248856,RMVar_hsa_circ_248858,RMVar_hsa_circ_117994,RMVar_hsa_circ_270526,RMVar_hsa_circ_14930,RMVar_hsa_circ_25220,RMVar_hsa_circ_248859,RMVar_hsa_circ_297156 115148 RMVar_ID_115148 Human_SNP_ID_870852659 m1A Human chr7 + 100124834 100124834 100124834 GAGGAGGAGGAAGAGGAGGAAGAGGAAGGGGGAGACAAGATGACCAAGACAGGAAGCCACCCCAA GAGGAGGAGGAAGAGGAGGAAGAGGAAGGGGGGGACAAGATGACCAAGACAGGAAGCCACCCCAA A G CNPY4 Ensembl:ENSG00000166997 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:100124783..100124909 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_22775009 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795,RMVar_hsa_circ_247064,RMVar_hsa_circ_127948 115149 RMVar_ID_115149 Human_SNP_ID_870854933 m1A Human chr7 - 5217914 5217914 5217914 GAGCCGGAATCATGTTTGCAGCTCTCTGAAAAAGGGACACCAATAAAGAGTGGCCACCGCACAGT GAGCCGGAATCATGTTTGCAGCTCTCTGAAAAGGGGACACCAATAAAGAGTGGCCACCGCACAGT T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:5217911..5218111 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SARC 1 - 115150 RMVar_ID_115150 Human_SNP_ID_870864275 m1A Human chr7 + 100033445 100033445 100033445 AGAAACGTGACCAGGAGGGCAAAACAGGAGAAAGACAGCAGAAAAACCCTGAGGAGAAAACCAGG AGAAACGTGACCAGGAGGGCAAAACAGGAGAAGGACAGCAGAAAAACCCTGAGGAGAAAACCAGG A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100033395..100033525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 THCA 1 - Human_RBP_ID_83825,Human_RBP_ID_843916,Human_RBP_ID_3120208,Human_RBP_ID_22111862,Human_RBP_ID_24549292,Human_RBP_ID_26356769 RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_86452,RMVar_hsa_circ_246994,RMVar_hsa_circ_246996 115151 RMVar_ID_115151 Human_SNP_ID_870872478 m1A Human chr7 - 100091065 100091065 100091065 AATGCGTTCCGCTTCCTCTGTGGCCAGAGTGTAGGTCAGCTCAGCAAACAGCATTGTGGCCTACA AATGCGTTCCGCTTCCTCTGTGGCCAGAGTGTGGGTCAGCTCAGCAAACAGCATTGTGGCCTACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:100091051..100091075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 115152 RMVar_ID_115152 Human_SNP_ID_870890217 m1A Human chr7 - 131556398 131556398 131556398 CTACCGCCCGGACGCGCGGATCCTCCGCCGGCACCGCAGCCACCTGCTCCCGGCCCAGAGGCGAC CTACCGCCCGGACGCGCGGATCCTCCGCCGGCGCCGCAGCCACCTGCTCCCGGCCCAGAGGCGAC T C PODXL Ensembl:ENSG00000128567 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:131556351..131556600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_98583,RMVar_hsa_circ_376614 115153 RMVar_ID_115153 Human_SNP_ID_870938248 m1A Human chr7 - 25123778 25123777 25123778 AGAATCCCAAGAAGTACATCCCTGGAACAAAAATGATCTTTGTCGGCATTAAGAAGAAGGAAGAA AGAATCCCAAGAAGTACATCCCTGGAACAAAA_TGATCTTTGTCGGCATTAAGAAGAAGGAAGAA AT A CYCS Ensembl:ENSG00000172115 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:25123776..25123800 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_3082363,Human_RBP_ID_9403214,Human_RBP_ID_26355949,Human_RBP_ID_27829216 Human_Splice_Rec_850816,Human_Splice_Rec_850820,Human_Splice_Rec_850826,Human_Splice_Rec_850832 115154 RMVar_ID_115154 Human_SNP_ID_870938454 m1A Human chr7 + 141742226 141742226 141742226 AGTCCGAAACAACTACCAGTTTGGTTCTTGAAAGATGTAAGTAGCTAATTTCCAAGTTTAAAATG AGTCCGAAACAACTACCAGTTTGGTTCTTGAATGATGTAAGTAGCTAATTTCCAAGTTTAAAATG A T SSBP1 Ensembl:ENSG00000106028 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:141742176..141742250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast metaplastic_carcinoma 6 breast Human_RBP_ID_3972660,Human_RBP_ID_24197348 Human_Splice_Rec_931114,Human_Splice_Rec_931115,Human_Splice_Rec_931128,Human_Splice_Rec_931129,Human_Splice_Rec_931140,Human_Splice_Rec_931141,Human_Splice_Rec_931152,Human_Splice_Rec_931153,Human_Splice_Rec_931164,Human_Splice_Rec_931165,Human_Splice_Rec_931176,Human_Splice_Rec_931177,Human_Splice_Rec_931188,Human_Splice_Rec_931189,Human_Splice_Rec_931204,Human_Splice_Rec_931205,Human_Splice_Rec_931216,Human_Splice_Rec_931217,Human_Splice_Rec_931228,Human_Splice_Rec_931229,Human_Splice_Rec_931240,Human_Splice_Rec_931244,Human_Splice_Rec_931245 RMVar_hsa_circ_86085,RMVar_hsa_circ_55931,RMVar_hsa_circ_64667,RMVar_hsa_circ_249210 115155 RMVar_ID_115155 Human_SNP_ID_870977786 m1A Human chr7 + 151035741 151035741 151035741 CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCAGGTACCGGCATTCCTGGCCATCCTCTTCACCC CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCTGGTACCGGCATTCCTGGCCATCCTCTTCACCC A T ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:151035707..151035790;chr7:151035712..151035785 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_19137633 Human_Splice_Rec_937547,Human_Splice_Rec_937581,Human_Splice_Rec_937609,Human_Splice_Rec_937683,Human_Splice_Rec_937709,Human_Splice_Rec_937739,Human_Splice_Rec_937769,Human_Splice_Rec_937787,Human_Splice_Rec_937815 RMVar_hsa_circ_11538,RMVar_hsa_circ_60337 115156 RMVar_ID_115156 Human_SNP_ID_870977811 m1A Human chr7 + 151035741 151035741 151035741 CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCAGGTACCGGCATTCCTGGCCATCCTCTTCACCC CCTCCGAAAATTGTCTCGCCAGTGTCAGGAGCGGGTACCGGCATTCCTGGCCATCCTCTTCACCC A G ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:151035707..151035790;chr7:151035712..151035785 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue Human_RBP_ID_19137633 Human_Splice_Rec_937547,Human_Splice_Rec_937581,Human_Splice_Rec_937609,Human_Splice_Rec_937683,Human_Splice_Rec_937709,Human_Splice_Rec_937739,Human_Splice_Rec_937769,Human_Splice_Rec_937787,Human_Splice_Rec_937815 RMVar_hsa_circ_11538,RMVar_hsa_circ_60337 115157 RMVar_ID_115157 Human_SNP_ID_870978606 m1A Human chr7 + 65113154 65113154 65113154 AAAAGGAGGGAGGGAGGAAAGGAGAAAAGGAAAGAAAACAAGAAAGTGAGAAAGAAAGAATAAGA AAAAGGAGGGAGGGAGGAAAGGAGAAAAGGAAGGAAAACAAGAAAGTGAGAAAGAAAGAATAAGA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:65113074..65113230 26863196 MeRIP-seq:(Medium) rs63749631 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_10905,GWAS_ID_10906 115158 RMVar_ID_115158 Human_SNP_ID_870979115 m1A Human chr7 - 116862574 116862571 116862574 TTCTGGCGACAAACCGCGGCGGCGGCGGCGGCAGCGGCCACCTGACTTCCCCGTTTCCGTGCGGT TTCTGGCGACAAACCGCGGCGGCGGCGGCGGC___GGCCACCTGACTTCCCCGTTTCCGTGCGGT CGCT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:116862526..116862699 26863196 MeRIP-seq:(Medium) rs754710280 Functional Loss DEL TCGA 33..35 33 COAD 1 - 115159 RMVar_ID_115159 Human_SNP_ID_870987984 m1A Human chr7 + 26196364 26196362 26196364 AATGAAAACCTAATCATATTTAAAATAAAAGCACACTCATCCTTTAAACACGTAGAACTTGAAAC AATGAAAACCTAATCATATTTAAAATAAAAG__CACTCATCCTTTAAACACGTAGAACTTGAAAC GCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HeLa cell line,mRNA;HEK293T,Starvation treatment chr7:26196361..26196640;chr7:26196361..26196481 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 STAD 1 - 115160 RMVar_ID_115160 Human_SNP_ID_871002397 m1A Human chr7 + 100430812 100430812 100430812 GCCACTCAAGACTGGTCGGAAGCGGCATAGACACCGGGGACAGCACCACCAGCAGCAGCAGGCAG GCCACTCAAGACTGGTCGGAAGCGGCATAGACGCCGGGGACAGCACCACCAGCAGCAGCAGGCAG A G MEPCE Ensembl:ENSG00000146834 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:100430627..100430975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_5512332,Human_RBP_ID_15944985,Human_RBP_ID_26772076,Human_RBP_ID_27102734,Human_RBP_ID_27527156 115161 RMVar_ID_115161 Human_SNP_ID_871005872 m1A Human chr7 + 44581526 44581526 44581526 CAGACAGATTTGATGGTCACCGGGCGTGTGGGAGGTGAACGTGAAGCGGCCCTCCGAGCCGTACT CAGACAGATTTGATGGTCACCGGGCGTGTGGGGGGTGAACGTGAAGCGGCCCTCCGAGCCGTACT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:44581476..44581550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney RMVar_hsa_circ_244967 115162 RMVar_ID_115162 Human_SNP_ID_871017391 m1A Human chr7 - 24623614 24623614 24623614 ATAAAAACAAACAAACAAACAAACAAACAAAAACCCTTAAATTTCAAGCCGTTATGGAGTAAGAT ATAAAAACAAACAAACAAACAAACAAACAAAACCCCTTAAATTTCAAGCCGTTATGGAGTAAGAT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr7:24623611..24623688;chr7:24623611..24623724 26863196 MeRIP-seq:(Medium) rs1047255555 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung 115163 RMVar_ID_115163 Human_SNP_ID_871024291 m1A Human chr7 - 26193696 26193696 26193696 TTAAGTGATTACTTAAAGGCTTATTTTATAATAGGTGGCAATTTTGGAGGTAGCCCCGGTTATGG TTAAGTGATTACTTAAAGGCTTATTTTATAATGGGTGGCAATTTTGGAGGTAGCCCCGGTTATGG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:26193481..26193700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,lung small_cell_carcinoma 8 lung,stomach Human_RBP_ID_14354,Human_RBP_ID_84110,Human_RBP_ID_16124338,Human_RBP_ID_23075501,Human_RBP_ID_23120581,Human_RBP_ID_26095456 RMVar_hsa_circ_80785,RMVar_hsa_circ_64349,RMVar_hsa_circ_84857,RMVar_hsa_circ_41110,RMVar_hsa_circ_352214,RMVar_hsa_circ_38135,RMVar_hsa_circ_311717,RMVar_hsa_circ_353243,RMVar_hsa_circ_357594,RMVar_hsa_circ_128060,RMVar_hsa_circ_74737,RMVar_hsa_circ_244215,RMVar_hsa_circ_244216,RMVar_hsa_circ_374972,RMVar_hsa_circ_121607,RMVar_hsa_circ_366603,RMVar_hsa_circ_244218,RMVar_hsa_circ_244219,RMVar_hsa_circ_316523,RMVar_hsa_circ_338242,RMVar_hsa_circ_86649,RMVar_hsa_circ_244223,RMVar_hsa_circ_244224,RMVar_hsa_circ_244225,RMVar_hsa_circ_244222,RMVar_hsa_circ_244226 115164 RMVar_ID_115164 Human_SNP_ID_871079506 m1A Human chr7 - 99419417 99419417 99419417 CGCCAGCCTCAGCCAGAGCAGCCACGACAGCCACAGTGTGTGCACTCGATGATGCGGCCCTGCAA CGCCAGCCTCAGCCAGAGCAGCCACGACAGCCGCAGTGTGTGCACTCGATGATGCGGCCCTGCAA T C PTCD1 Ensembl:ENSG00000106246 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:99419268..99419418 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_18107368 115165 RMVar_ID_115165 Human_SNP_ID_871094211 m1A Human chr7 - 158973747 158973747 158973747 CACACATCTCCATCTGAGATGCAGAAACGCTAACCGGGTCCCTGCCACACGTCAAACGTCGGCGC CACACATCTCCATCTGAGATGCAGAAACGCTAGCCGGGTCCCTGCCACACGTCAAACGTCGGCGC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:158973413..158973800 26863196 MeRIP-seq:(Medium) rs2527220 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115166 RMVar_ID_115166 Human_SNP_ID_871099243 m1A Human chr7 - 23512895 23512895 23512895 TGTGTATTTTGAGAGAATAGATGACTCAAAGGAGGTAAATTTGTCTTTTATATGCCTGATTATAG TGTGTATTTTGAGAGAATAGATGACTCAAAGGGGGTAAATTTGTCTTTTATATGCCTGATTATAG T C TRA2A Ensembl:ENSG00000164548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:23512876..23512900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 6 uterus Human_RBP_ID_1069857,Human_RBP_ID_2040020,Human_RBP_ID_5401449,Human_RBP_ID_9351031,Human_RBP_ID_19019484,Human_RBP_ID_24207938 Human_Splice_Rec_849731,Human_Splice_Rec_849749,Human_Splice_Rec_849765,Human_Splice_Rec_849781,Human_Splice_Rec_849807,Human_Splice_Rec_849815 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_269242,RMVar_hsa_circ_244132,RMVar_hsa_circ_265866,RMVar_hsa_circ_244133,RMVar_hsa_circ_285379,RMVar_hsa_circ_335045,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_319385,RMVar_hsa_circ_13288,RMVar_hsa_circ_244135 115167 RMVar_ID_115167 Human_SNP_ID_871118846 m1A Human chr7 - 130070706 130070706 130070706 CCACTGCCCCCGCCGGCCCCGCTACCTCCGCCACCAGCGCCGGCGGCGCCTCCTCCCCTCCGGCG CCACTGCCCCCGCCGGCCCCGCTACCTCCGCCCCCAGCGCCGGCGGCGCCTCCTCCCCTCCGGCG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:130070560..130070728;chr7:130070509..130070809;chr7:130070559..130070750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 115168 RMVar_ID_115168 Human_SNP_ID_871128060 m1A Human chr7 - 102567952 102567952 102567952 ACGGGGTGGGCTGGACACTGGCCCGTGTGCCCAGGCCTGGGACAGCCCTGGCCTGTTTCTTCGGA ACGGGGTGGGCTGGACACTGGCCCGTGTGCCCGGGCCTGGGACAGCCCTGGCCTGTTTCTTCGGA T C POLR2J3,AC093668.1,POLR2J3:2 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249,Ensembl:ENSG00000285437 Protein coding,Protein coding,Protein coding CDS,intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs200859434 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue RMVar_hsa_circ_28775,RMVar_hsa_circ_97247,RMVar_hsa_circ_247346,RMVar_hsa_circ_96796,RMVar_hsa_circ_120312,RMVar_hsa_circ_247349,RMVar_hsa_circ_116919,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354,RMVar_hsa_circ_119166,RMVar_hsa_circ_247356 115169 RMVar_ID_115169 Human_SNP_ID_871132277 m1A Human chr7 + 6272552 6272552 6272552 CCCGCAGCCGGCGAGCCGGGGGCCGGCAGCAGAGGGGCCGCGGGCTGGGGACGCCGCCGGAGGGA CCCGCAGCCGGCGAGCCGGGGGCCGGCAGCAGGGGGGCCGCGGGCTGGGGACGCCGCCGGAGGGA A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:6272476..6272650 26863410 MeRIP-seq:(Medium) rs1178088452 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115170 RMVar_ID_115170 Human_SNP_ID_871150321 m1A Human chr7 - 44568207 44568207 44568207 CCTCTTCCCCCGGCAGACATACTTTGAAGACAACCCTAGGGACCTCCAGCTGCTGCGGCATGACC CCTCTTCCCCCGGCAGACATACTTTGAAGACAGCCCTAGGGACCTCCAGCTGCTGCGGCATGACC T C DDX56 Ensembl:ENSG00000136271 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:44568101..44568269 26863410 MeRIP-seq:(Medium) rs764434931 Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_952461,Human_RBP_ID_1687041,Human_RBP_ID_2043350,Human_RBP_ID_3847394,Human_RBP_ID_3970874,Human_RBP_ID_5403949,Human_RBP_ID_7741685,Human_RBP_ID_8911029,Human_RBP_ID_9403347,Human_RBP_ID_16163837,Human_RBP_ID_18171877,Human_RBP_ID_18540217,Human_RBP_ID_19020731,Human_RBP_ID_22685384,Human_RBP_ID_22747057,Human_RBP_ID_26546876,Human_RBP_ID_27531798 Human_Splice_Rec_862958,Human_Splice_Rec_862959,Human_Splice_Rec_862984,Human_Splice_Rec_862985,Human_Splice_Rec_863010,Human_Splice_Rec_863011,Human_Splice_Rec_863038,Human_Splice_Rec_863039,Human_Splice_Rec_863062,Human_Splice_Rec_863063,Human_Splice_Rec_863086,Human_Splice_Rec_863087,Human_Splice_Rec_863110,Human_Splice_Rec_863111,Human_Splice_Rec_863120,Human_Splice_Rec_863121,Human_Splice_Rec_863142 Human_miRNA_ID_2293788 RMVar_hsa_circ_98480,RMVar_hsa_circ_269065,RMVar_hsa_circ_102648,RMVar_hsa_circ_99813,RMVar_hsa_circ_244956,RMVar_hsa_circ_244958,RMVar_hsa_circ_92304,RMVar_hsa_circ_244957,RMVar_hsa_circ_13874,RMVar_hsa_circ_244955,RMVar_hsa_circ_83731,RMVar_hsa_circ_269245,RMVar_hsa_circ_244960 115171 RMVar_ID_115171 Human_SNP_ID_871174776 m1A Human chr7 + 114922892 114922891 114922892 CCCGCAGGGGTGGTGTGCTCTTCTCTAAAAACATTTTTTTTTTTAATTTTGTATATTTTTCCGCC CCCGCAGGGGTGGTGTGCTCTTCTCTAAAAAC_TTTTTTTTTTTAATTTTGTATATTTTTCCGCC CA C MDFIC Ensembl:ENSG00000135272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:114922889..114923158 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - Human_RBP_ID_7682342 115172 RMVar_ID_115172 Human_SNP_ID_871213202 m1A Human chr7 - 45073552 45073552 45073552 AGCGGAGGCCTACCGTCAGCATGTAGTCCTGCAGCAGCTCAGTGGCGCTGGCGCTCAGCTCGCTC AGCGGAGGCCTACCGTCAGCATGTAGTCCTGCGGCAGCTCAGTGGCGCTGGCGCTCAGCTCGCTC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:45073501..45073602 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115173 RMVar_ID_115173 Human_SNP_ID_871242904 m1A Human chr7 + 66995352 66995352 66995352 TTGTAGCAGGCGATTTCGAAGCGCTTCCCGGCACGCTTCATCCGTACCACGGCCACATTGGTTAG TTGTAGCAGGCGATTTCGAAGCGCTTCCCGGCGCGCTTCATCCGTACCACGGCCACATTGGTTAG A G TYW1 Ensembl:ENSG00000198874 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:66995258..66995366 26863196 MeRIP-seq:(Medium) rs774593246 Functional Loss SNV ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 115174 RMVar_ID_115174 Human_SNP_ID_871250304 m1A Human chr7 - 77618536 77618535 77618536 TACCTGCGGGTCCTTGGTGGTTTTGGAGGAGGAGAATCTTGTTTTTCAGGCTCTATGGAGCTGAC TACCTGCGGGTCCTTGGTGGTTTTGGAGGAGG_GAATCTTGTTTTTCAGGCTCTATGGAGCTGAC CT C APTR RNACentral:URS0000D5A265 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:77618488..77626778 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 115175 RMVar_ID_115175 Human_SNP_ID_871273957 m1A Human chr7 - 76997162 76997162 76997162 CCCACCTCCACACACCTCACACCCCACCTCACACCCCACACACTTCTACACACCCTACACACCTC CCCACCTCCACACACCTCACACCCCACCTCACCCCCCACACACTTCTACACACCCTACACACCTC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:76997003..76997204 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - 115176 RMVar_ID_115176 Human_SNP_ID_871276225 m1A Human chr7 - 151080766 151080766 151080766 GCTGGGAAGATGGCGGACTCGGTGGCTAGCCGATGAGGAGGCCGCGGGGGGAACCCGGCCCCCGG GCTGGGAAGATGGCGGACTCGGTGGCTAGCCGGTGAGGAGGCCGCGGGGGGAACCCGGCCCCCGG T C FASTK Ensembl:ENSG00000164896 Protein coding start codon GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr7:151080476..151080825;chr7:151080268..151080850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 salivary_gland salivary_duct_carcinoma 4 head and neck Human_RBP_ID_254455,Human_RBP_ID_4931073,Human_RBP_ID_9440322,Human_RBP_ID_18426120,Human_RBP_ID_18466196,Human_RBP_ID_18504321,Human_RBP_ID_23116963,Human_RBP_ID_23120632,Human_RBP_ID_26793718,Human_RBP_ID_27107936 Human_Splice_Rec_938247,Human_Splice_Rec_938277,Human_Splice_Rec_938307,Human_Splice_Rec_938323,Human_Splice_Rec_938341,Human_Splice_Rec_938363,Human_Splice_Rec_938401 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 115177 RMVar_ID_115177 Human_SNP_ID_871279379 m1A Human chr7 + 66950992 66950992 66950992 CGCACTGTGTTCCTGACACGTACAGCAACGCCACGCTCTGGTACAAGATCTTCACAACTGCCAGA CGCACTGTGTTCCTGACACGTACAGCAACGCCGCGCTCTGGTACAAGATCTTCACAACTGCCAGA A G TMEM248 Ensembl:ENSG00000106609 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:66950988..66951139 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_2045579,Human_RBP_ID_9404489,Human_RBP_ID_16199015,Human_RBP_ID_17315597,Human_RBP_ID_17427337,Human_RBP_ID_21397032 Human_Splice_Rec_871706,Human_Splice_Rec_871742 RMVar_hsa_circ_77754,RMVar_hsa_circ_111417,RMVar_hsa_circ_245392,RMVar_hsa_circ_300641,RMVar_hsa_circ_288937,RMVar_hsa_circ_126075,RMVar_hsa_circ_245396,RMVar_hsa_circ_245397,RMVar_hsa_circ_111660,RMVar_hsa_circ_245400,RMVar_hsa_circ_371739,RMVar_hsa_circ_359883,RMVar_hsa_circ_245404,RMVar_hsa_circ_245401,RMVar_hsa_circ_245402,RMVar_hsa_circ_86399,RMVar_hsa_circ_286317,RMVar_hsa_circ_294730,RMVar_hsa_circ_245405,RMVar_hsa_circ_245403 115178 RMVar_ID_115178 Human_SNP_ID_871297260 m1A Human chr7 - 100430644 100430644 100430644 GAAGGGGGGATGACTTAGGGGTCTCCGCGTTGAGAGTGCGGCTCACTTCCTCATCCAGGAGGCTA GAAGGGGGGATGACTTAGGGGTCTCCGCGTTGTGAGTGCGGCTCACTTCCTCATCCAGGAGGCTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:100430601..100431246 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 115179 RMVar_ID_115179 Human_SNP_ID_871309431 m1A Human chr7 - 44766263 44766263 44766263 GGAGGCTGCTGGGAATGTCAGACTGGTAGGAGATGGGGGGTGGTCCCGGGGTGAACTCAGCAAGG GGAGGCTGCTGGGAATGTCAGACTGGTAGGAGGTGGGGGGTGGTCCCGGGGTGAACTCAGCAAGG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:44766176..44766275 26863196 MeRIP-seq:(Medium) rs772185772 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver 115180 RMVar_ID_115180 Human_SNP_ID_871313013 m1A Human chr7 + 129213368 129213368 129213368 ACCCTGGGAAGCTGCCGTAGCTTCAGCCAGGCAAGAAAGCTTCCTTCAACCTGCATAGCCGGTGG ACCCTGGGAAGCTGCCGTAGCTTCAGCCAGGCCAGAAAGCTTCCTTCAACCTGCATAGCCGGTGG A C SMO Ensembl:ENSG00000128602 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:129213098..129213446 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115181 RMVar_ID_115181 Human_SNP_ID_871332311 m1A Human chr7 - 100429485 100429485 100429485 CCACCGTAGGCGGGGGACGGGAGCTGGTGTGAAAAGGTCTCCTTGACACCCGACCCTTGTTCCTG CCACCGTAGGCGGGGGACGGGAGCTGGTGTGATAAGGTCTCCTTGACACCCGACCCTTGTTCCTG T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:100429421..100429928 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 115182 RMVar_ID_115182 Human_SNP_ID_871354786 m1A Human chr7 - 74190229 74190228 74190229 GAGAGCTACCCATTCCTGAGGATACACAAAAAAGATAAAGTTGAGGTCGTGTCATTACCTTGCTG GAGAGCTACCCATTCCTGAGGATACACAAAAA_GATAAAGTTGAGGTCGTGTCATTACCTTGCTG CT C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:74190226..74190275;chr7:74190226..74190325;chr7:74190226..74190300 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - 115183 RMVar_ID_115183 Human_SNP_ID_871374498 m1A Human chr7 + 151028557 151028557 151028557 CATTTATTTCGGGTCGGGATTCGGGGTGGCCCATTCCCAGGCAGGCTGCTACCGCCCCTCCGCTT CATTTATTTCGGGTCGGGATTCGGGGTGGCCCCTTCCCAGGCAGGCTGCTACCGCCCCTCCGCTT A C ABCB8 Ensembl:ENSG00000197150 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:151028451..151028669 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_254559,Human_RBP_ID_794562,Human_RBP_ID_18451318,Human_RBP_ID_22426661 Human_Splice_Rec_937539,Human_Splice_Rec_937567,Human_Splice_Rec_937571,Human_Splice_Rec_937601,Human_Splice_Rec_937631,Human_Splice_Rec_937639,Human_Splice_Rec_937645,Human_Splice_Rec_937647,Human_Splice_Rec_937653,Human_Splice_Rec_937671,Human_Splice_Rec_937703,Human_Splice_Rec_937729,Human_Splice_Rec_937759,Human_Splice_Rec_937777,Human_Splice_Rec_937795,Human_Splice_Rec_937799 115184 RMVar_ID_115184 Human_SNP_ID_871391191 m1A Human chr7 - 101222604 101222604 101222604 GCACCCGCCGCTGCCCGGGGTCCTGGGAGCGAACTGGATGGAGCAGGGCACGCAAAGTTACAGGG GCACCCGCCGCTGCCCGGGGTCCTGGGAGCGAGCTGGATGGAGCAGGGCACGCAAAGTTACAGGG T C RF00017-1028 RNACentral:URS00008FFE84 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr7:101222601..101222775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 115185 RMVar_ID_115185 Human_SNP_ID_871466834 m1A Human chr7 - 99425319 99425319 99425319 AGGCACTTGGGCCTCCAGAGCCTCCGGAAGCCAGAGTGCCCGGCAAGGCCCAACCAGAGGTGGAT AGGCACTTGGGCCTCCAGAGCCTCCGGAAGCCGGAGTGCCCGGCAAGGCCCAACCAGAGGTGGAT T C PTCD1,ATP5MF-PTCD1 Ensembl:ENSG00000106246,Ensembl:ENSG00000248919 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:99425268..99425566 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung RMVar_hsa_circ_80410,RMVar_hsa_circ_246949 115186 RMVar_ID_115186 Human_SNP_ID_871474730 m1A Human chr7 - 55743551 55743551 55743551 GCCCCTCCCACGCTGACCCCTTGCCTCACACCAGCCCCTCCCATGCTGACCCCTTGCCTCACACG GCCCCTCCCACGCTGACCCCTTGCCTCACACCGGCCCCTCCCATGCTGACCCCTTGCCTCACACG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:55743500..55743592 26863196 MeRIP-seq:(Medium) rs558962637 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115187 RMVar_ID_115187 Human_SNP_ID_871482243 m1A Human chr7 + 56079635 56079634 56079635 GGAGCTGTAAGCAGCCGGGTGGTGACAAGGAGAAAAGCCTTCTAGGGTCACTGTCATTCCCTGGC GGAGCTGTAAGCAGCCGGGTGGTGACAAGGAG_AAAGCCTTCTAGGGTCACTGTCATTCCCTGGC GA G SUMF2 Ensembl:ENSG00000129103 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:56079584..56079727 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_686220,Human_RBP_ID_22463101,Human_RBP_ID_27114960 RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_111137,RMVar_hsa_circ_245239,RMVar_hsa_circ_245240 115188 RMVar_ID_115188 Human_SNP_ID_871487222 m1A Human chr7 + 105377158 105377158 105377158 CACTGCTGACCACGCCCTTCTTGAAATGCTGTATTCCCTTGGTTTCTGTAAGACAACTTTCTCCT CACTGCTGACCACGCCCTTCTTGAAATGCTGTGTTCCCTTGGTTTCTGTAAGACAACTTTCTCCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:105377155..105377306 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 115189 RMVar_ID_115189 Human_SNP_ID_871503490 m1A Human chr7 + 128862984 128862984 128862984 GGTGACTGGTTTCCTGCTGGGCGGCATAGGGGAGCTTAACAAGAACCGCCATCCCAATTTCCTGG GGTGACTGGTTTCCTGCTGGGCGGCATAGGGGTGCTTAACAAGAACCGCCATCCCAATTTCCTGG A T ATP6V1F Ensembl:ENSG00000128524 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:128862895..128862984 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_253351,Human_RBP_ID_674794,Human_RBP_ID_4924174,Human_RBP_ID_5122902,Human_RBP_ID_5153307,Human_RBP_ID_5328017,Human_RBP_ID_8944197,Human_RBP_ID_9204184,Human_RBP_ID_17665454,Human_RBP_ID_18426563,Human_RBP_ID_22111218,Human_RBP_ID_22515162,Human_RBP_ID_24189171,Human_RBP_ID_27105014 Human_Splice_Rec_921451,Human_Splice_Rec_921453 RMVar_hsa_circ_113647,RMVar_hsa_circ_248294 115190 RMVar_ID_115190 Human_SNP_ID_871504748 m1A Human chr7 - 151076830 151076830 151076830 GTAACCTGCCGCCCTCTCCTCTCCCCACAGCTACCCTTCGAGGAACTGGAGTCCCAGAGAGGCCT GTAACCTGCCGCCCTCTCCTCTCCCCACAGCTGCCCTTCGAGGAACTGGAGTCCCAGAGAGGCCT T C FASTK Ensembl:ENSG00000164896 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:151076813..151076950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 4 biliary tract,gallbladder Human_RBP_ID_678868,Human_RBP_ID_18171804,Human_RBP_ID_22319331,Human_RBP_ID_22687570,Human_RBP_ID_26132390 Human_Splice_Rec_938276,Human_Splice_Rec_938294,Human_Splice_Rec_938306,Human_Splice_Rec_938322,Human_Splice_Rec_938340,Human_Splice_Rec_938354,Human_Splice_Rec_938362,Human_Splice_Rec_938378,Human_Splice_Rec_938390,Human_Splice_Rec_938396 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 115191 RMVar_ID_115191 Human_SNP_ID_871521234 m1A Human chr7 + 19117151 19117151 19117151 CTGCCCGGCTCGTCGCCGCCTCCGACGCCCCCACCCGCGGCTCCGCCGGGCCCCGCGCCGCCGCC CTGCCCGGCTCGTCGCCGCCTCCGACGCCCCCCCCCGCGGCTCCGCCGGGCCCCGCGCCGCCGCC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr7:19117045..19117239 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,pancreas ductal_carcinoma 2 pancreas 115192 RMVar_ID_115192 Human_SNP_ID_871521534 m1A Human chr7 - 76997508 76997508 76997508 CACAGACCCCACACTCCACACCTCCACACACCACACACCTCCACACCTCACACATCTCCACACCC CACAGACCCCACACTCCACACCTCCACACACCCCACACCTCCACACCTCACACATCTCCACACCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:76997506..76997673 26863196 MeRIP-seq:(Medium) rs200463551 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115193 RMVar_ID_115193 Human_SNP_ID_871537986 m1A Human chr7 + 132975202 132975202 132975202 AGGTGCTTTGCCTTAGCGCGTTCCTCCTCGCTACATATCCTCTCCCGAAGGATGGCTCTGGTTAA AGGTGCTTTGCCTTAGCGCGTTCCTCCTCGCTCCATATCCTCTCCCGAAGGATGGCTCTGGTTAA A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:132973958..132975202 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115194 RMVar_ID_115194 Human_SNP_ID_871546264 m1A Human chr7 + 5529569 5529569 5529569 GGTGCCTGGGGCGCCCCACGATGGAGGGGAAGACGGCCCGGGGGGCATCGTCGCCCGCGAAGCCG GGTGCCTGGGGCGCCCCACGATGGAGGGGAAGCCGGCCCGGGGGGCATCGTCGCCCGCGAAGCCG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:5529385..5529875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115195 RMVar_ID_115195 Human_SNP_ID_871575303 m1A Human chr7 + 158975588 158975586 158975588 TACAGGCGGTGTCAGCTGGAGAGACAGGAGTCAAAACTCAAATCCGTCCCGCCTTCCCGGCTAAA TACAGGCGGTGTCAGCTGGAGAGACAGGAGT__AAACTCAAATCCGTCCCGCCTTCCCGGCTAAA TCA T lnc-WDR60-3,lnc-WDR60-3:2,lnc-WDR60-3:3 RNACentral:URS00008BE388,RNACentral:URS00008C144D,RNACentral:URS00008BDFD7 lincRNA,lincRNA,lincRNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:158975572..158975675 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - 115196 RMVar_ID_115196 Human_SNP_ID_871609361 m1A Human chr7 + 23455297 23455297 23455297 TCACCATCCTGCCTCACACTCCAGCCTCTTTAATCTCAAACAGCTTGTAGTTCCCACACACACCC TCACCATCCTGCCTCACACTCCAGCCTCTTTAGTCTCAAACAGCTTGTAGTTCCCACACACACCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:23455256..23455446 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115197 RMVar_ID_115197 Human_SNP_ID_871642873 m1A Human chr7 - 139284101 139284101 139284101 AATAAGTTTAGTTGATACTGAAGGCTTAGCTGACAGAGAGGGCTTGGGTGAGGCAGAAGGCTTAG AATAAGTTTAGTTGATACTGAAGGCTTAGCTGTCAGAGAGGGCTTGGGTGAGGCAGAAGGCTTAG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:139284050..139284116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 115198 RMVar_ID_115198 Human_SNP_ID_871662639 m1A Human chr7 - 100888589 100888589 100888589 AAAATTCTCAGAGCTTCATAGGACAAGGTAGTACAAGTATGGATGATACAGGACTGAGGAACGGG AAAATTCTCAGAGCTTCATAGGACAAGGTAGTGCAAGTATGGATGATACAGGACTGAGGAACGGG T C RF00017-4590 RNACentral:URS0000965567 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:100888538..100888609 26863196 MeRIP-seq:(Medium) rs1014503997 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 115199 RMVar_ID_115199 Human_SNP_ID_871666374 m1A Human chr7 + 100097939 100097939 100097939 CACAATCCGATGGGCTTCCAGGTAGGTTTCTGAGAGTAAACCCTTGGGCAGGAAAATGCCAGGAT CACAATCCGATGGGCTTCCAGGTAGGTTTCTGCGAGTAAACCCTTGGGCAGGAAAATGCCAGGAT A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:100097826..100097950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115200 RMVar_ID_115200 Human_SNP_ID_871686278 m1A Human chr7 + 94509873 94509873 94509873 CACGGCGGAGCAGCGGCGGCGGGGCTGGGGGGAGGCCGCCGAGTCGGCCGCGGCCGAGGAGGGGC CACGGCGGAGCAGCGGCGGCGGGGCTGGGGGGGGGCCGCCGAGTCGGCCGCGGCCGAGGAGGGGC A G CASD1 Ensembl:ENSG00000127995 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr7:94509812..94510065 26863196 MeRIP-seq:(Medium) rs939043585 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4955871,Human_RBP_ID_9354766,Human_RBP_ID_18426048,Human_RBP_ID_22463616 115201 RMVar_ID_115201 Human_SNP_ID_871710952 m1A Human chr7 + 39566450 39566450 39566450 GATGTCGTGGGTTCAAGCAGCCTCCTTGATCCAGGGCCCTGGAGACAAAGGGGACGTGTTTGACG GATGTCGTGGGTTCAAGCAGCCTCCTTGATCCGGGGCCCTGGAGACAAAGGGGACGTGTTTGACG A G YAE1 Ensembl:ENSG00000241127 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr7:39566401..39566552;chr7:39566401..39566596;chr7:39566401..39566605;chr7:39566401..39566595 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_1686448,Human_RBP_ID_4956281 Human_Splice_Rec_859377,Human_Splice_Rec_859379,Human_Splice_Rec_859383,Human_Splice_Rec_859387 115202 RMVar_ID_115202 Human_SNP_ID_871727417 m1A Human chr7 + 5388372 5388372 5388372 CCGAAGAGCTTGGCGGCCTGTTGGGCTGCAGGACCGGCTGGGCCGCGGGGCGCACGCTCGCAGGG CCGAAGAGCTTGGCGGCCTGTTGGGCTGCAGGGCCGGCTGGGCCGCGGGGCGCACGCTCGCAGGG A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated chr7:5388330..5388500;chr7:5388324..5388409 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115203 RMVar_ID_115203 Human_SNP_ID_871793779 m1A Human chr7 - 27185036 27185036 27185036 ATTTCTCCAGCCTCCCTTCTTTTCTGCCCCAGACCCCGTCTTCGCGCCCAATGACATACTCCTAC ATTTCTCCAGCCTCCCTTCTTTTCTGCCCCAGTCCCCGTCTTCGCGCCCAATGACATACTCCTAC T A HOXA11 Ensembl:ENSG00000005073 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr7:27184928..27185174 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain Human_RBP_ID_27112147 115204 RMVar_ID_115204 Human_SNP_ID_871801162 m1A Human chr7 - 107891291 107891291 107891291 TGGCTCAACACGACCTCACCTACTCGGCCCTCACCTTGGCCAAGGAGCAGTACACACGACTCCAG TGGCTCAACACGACCTCACCTACTCGGCCCTCTCCTTGGCCAAGGAGCAGTACACACGACTCCAG T A - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:107891191..107891295 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 115205 RMVar_ID_115205 Human_SNP_ID_871803221 m1A Human chr7 + 73539956 73539956 73539956 CCGTGCGGAAGTCGGAGGTGTGTGCTGGGCTCAGGGACTCACTCTGCTGGGGGCTGGGGCTTGAG CCGTGCGGAAGTCGGAGGTGTGTGCTGGGCTCGGGGACTCACTCTGCTGGGGGCTGGGGCTTGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr7:73539855..73540050;chr7:73539844..73540075;chr7:73539830..73540112 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 3 stomach 115206 RMVar_ID_115206 Human_SNP_ID_871809388 m1A Human chr7 + 98281926 98281926 98281926 CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTACCTCGTCACAGGTGGGCCCGTAACCAACTTTC CCCCGCCGCGCCCCCGCCGCCGCCCTACCCCTGCCTCGTCACAGGTGGGCCCGTAACCAACTTTC A G BRI3 Ensembl:ENSG00000164713 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr7:98281876..98281950 26863196 MeRIP-seq:(Medium) rs1469279706 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_17427020 Human_Splice_Rec_893523,Human_Splice_Rec_893527,Human_Splice_Rec_893531,Human_Splice_Rec_893533 Human_miRNA_ID_1913995,Human_miRNA_ID_1916446,Human_miRNA_ID_1918895,Human_miRNA_ID_1921352,Human_miRNA_ID_1923810,Human_miRNA_ID_1926260,Human_miRNA_ID_1928712,Human_miRNA_ID_1931164,Human_miRNA_ID_2628993,Human_miRNA_ID_2642102,Human_miRNA_ID_3124845 RMVar_hsa_circ_95022,RMVar_hsa_circ_246779 115207 RMVar_ID_115207 Human_SNP_ID_871843085 m1A Human chr7 + 5530460 5530460 5530460 CTGCGGCCCAGACGGCGGCTCTGCACGGGCGAAGGGGCCGCGGCCGCCTGCGGCCGGGCCGTGAG CTGCGGCCCAGACGGCGGCTCTGCACGGGCGAGGGGGCCGCGGCCGCCTGCGGCCGGGCCGTGAG A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr7:5530454..5530625 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 115208 RMVar_ID_115208 Human_SNP_ID_871860415 m1A Human chr7 + 20798272 20798272 20798272 CCCGGGCGGGAAGGCTGCGCCGGCTCCCGCCAAGGGGGAGGCGCCACCCCGCCCCGGGGCGGTTG CCCGGGCGGGAAGGCTGCGCCGGCTCCCGCCAGGGGGGAGGCGCCACCCCGCCCCGGGGCGGTTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:20798199..20798285 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115209 RMVar_ID_115209 Human_SNP_ID_871866067 m1A Human chr7 + 134451702 134451702 134451702 CTGGTACACATGGGCACAGTCGATGTGGCGGTACCCGACGTCAATGGCCACCTTCACGGCCTCAG CTGGTACACATGGGCACAGTCGATGTGGCGGTGCCCGACGTCAATGGCCACCTTCACGGCCTCAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr7:134451651..134451790 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 2 stomach 115210 RMVar_ID_115210 Human_SNP_ID_871869088 m1A Human chr7 - 10938860 10938860 10938860 TCCCCCTCTTTGTATTTATTGGAACTGGAGCTACTGGAGCAACACTGTATCTCTTGCGTCTGGCA TCCCCCTCTTTGTATTTATTGGAACTGGAGCTTCTGGAGCAACACTGTATCTCTTGCGTCTGGCA T A NDUFA4 Ensembl:ENSG00000189043 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr7:10938801..10938900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_673059,Human_RBP_ID_793991,Human_RBP_ID_956657,Human_RBP_ID_1049851,Human_RBP_ID_1113594,Human_RBP_ID_1680397,Human_RBP_ID_2033047,Human_RBP_ID_3826644,Human_RBP_ID_4956995,Human_RBP_ID_5122710,Human_RBP_ID_5451745,Human_RBP_ID_7676426,Human_RBP_ID_8654648,Human_RBP_ID_9337058,Human_RBP_ID_15975032,Human_RBP_ID_17314471,Human_RBP_ID_17426908,Human_RBP_ID_17664971,Human_RBP_ID_18089218,Human_RBP_ID_21903957,Human_RBP_ID_22463023,Human_RBP_ID_22774288,Human_RBP_ID_23215410,Human_RBP_ID_24184046 Human_Splice_Rec_843864,Human_Splice_Rec_843865,Human_Splice_Rec_843872,Human_Splice_Rec_843873,Human_Splice_Rec_843878,Human_Splice_Rec_843879,Human_Splice_Rec_843881 RMVar_hsa_circ_112993,RMVar_hsa_circ_243776 115211 RMVar_ID_115211 Human_SNP_ID_871880813 m1A Human chr7 - 139035725 139035725 139035725 TGTGCGCCTCTGCGCCCGCTACCAGCGCGGCGAGTGCCAGGCCTGCGACCAGCTGCACTTCTGCC TGTGCGCCTCTGCGCCCGCTACCAGCGCGGCGGGTGCCAGGCCTGCGACCAGCTGCACTTCTGCC T C ZC3HAV1L Ensembl:ENSG00000146858 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr7:139035676..139035834 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_676704 Human_Splice_Rec_927951 115212 RMVar_ID_115212 Human_SNP_ID_872018338 m1A Human chr7 - 1010058 1010057 1010058 GGAGCAGAGGGTCCTGGAAAGGAAGCTGAAAAAGGAACGGAAGAAAGAGGAGAGGCAGCGTCTGC GGAGCAGAGGGTCCTGGAAAGGAAGCTGAAAA_GGAACGGAAGAAAGAGGAGAGGCAGCGTCTGC CT C C7orf50 Ensembl:ENSG00000146540 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 33..33 33 COAD,STAD 2 - Human_RBP_ID_672326,Human_RBP_ID_4957604,Human_RBP_ID_5122971,Human_RBP_ID_8944138,Human_RBP_ID_19019361,Human_RBP_ID_26357482,Human_RBP_ID_26550253 Human_Splice_Rec_837272,Human_Splice_Rec_837280,Human_Splice_Rec_837288,Human_Splice_Rec_837294,Human_Splice_Rec_837302,Human_Splice_Rec_837308,Human_Splice_Rec_837316 RMVar_hsa_circ_357195,RMVar_hsa_circ_1847,RMVar_hsa_circ_51160,RMVar_hsa_circ_377843 115213 RMVar_ID_115213 Human_SNP_ID_872036480 m1A Human chr7 - 128792250 128792248 128792251 GGCTGGCTGCGGGCTGGGGTGCAGAGGAAAGAAGGGGACATGTCTTCCAGCTCCTCGAGGCTCTG GGCTGGCTGCGGGCTGGGGTGCAGAGGAAAG___GGGACATGTCTTCCAGCTCCTCGAGGCTCTG CCTT C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr7:128792231..128792324 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 BRCA 1 - 115214 RMVar_ID_115214 Human_SNP_ID_872090216 m1A Human chr7 + 155318231 155318231 155318231 TAATCATCATCACCATCACCATCACTATCATCACCATCTCATCATCACTATCACCATCACCATCA TAATCATCATCACCATCACCATCACTATCATCTCCATCTCATCATCACTATCACCATCACCATCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr7:155318208..155318282 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115215 RMVar_ID_115215 Human_SNP_ID_872103537 m1A Human chr7 - 5622879 5622879 5622879 GGAGCACAACCTGCCCATGCACTTTGGCCCCCAGCCGCGGCATCGCTTCTGATGGCCCCGAATCC GGAGCACAACCTGCCCATGCACTTTGGCCCCCGGCCGCGGCATCGCTTCTGATGGCCCCGAATCC T C RNF216 Ensembl:ENSG00000011275 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr7:5622831..5623027 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_5533429 115216 RMVar_ID_115216 Human_SNP_ID_817774326 m1A Human chr13 - 48095047 48095047 48095047 AATGGCTGCGTCTTCGAGTGGTGAGAAGGAGAAGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCGG AATGGCTGCGTCTTCGAGTGGTGAGAAGGAGATGGAGCGGCTGGGAGGCGGTTTGGGAGTGGCGG T A MED4 Ensembl:ENSG00000136146 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr13:48094870..48095081;chr13:48094932..48095100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_9417305,Human_RBP_ID_18417725 Human_Splice_Rec_1463847,Human_Splice_Rec_1463871 RMVar_hsa_circ_163297,RMVar_hsa_circ_90989 115217 RMVar_ID_115217 Human_SNP_ID_817891185 m1A Human chr13 - 28138903 28138903 28138903 GCACCAGCCAGAGCCAGGGGGACGCTGTTGCTATGGAGGCCGAGGCCCGGGGCAGCCCCGGCGGC GCACCAGCCAGAGCCAGGGGGACGCTGTTGCTGTGGAGGCCGAGGCCCGGGGCAGCCCCGGCGGC T C PAN3-AS1,PAN3-AS1:2,PAN3-AS1:3,PAN3-AS1:4 RNACentral:URS00008C35BB,RNACentral:URS0000D59C08,RNACentral:URS0000D5A35D,RNACentral:URS000075C6DE lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:28138852..28174285 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 115218 RMVar_ID_115218 Human_SNP_ID_817919405 m1A Human chr13 - 33829925 33829925 33829925 CACTTTAGATGTAGAATTGCAGCACAAGATCAATCTGCAGGTAGACATATATTTTTCCATGGTTC CACTTTAGATGTAGAATTGCAGCACAAGATCATTCTGCAGGTAGACATATATTTTTCCATGGTTC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:33829876..33829925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 115219 RMVar_ID_115219 Human_SNP_ID_817943397 m1A Human chr13 - 95897966 95897966 95897966 TTACTGTGGATCAAGGTGAGGAAGGCTGCAGGATGAGTGAGGTTGTCAGGAGCAGTATAAGAAGA TTACTGTGGATCAAGGTGAGGAAGGCTGCAGGTTGAGTGAGGTTGTCAGGAGCAGTATAAGAAGA T A UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:95897917..95898140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_6311168,Human_RBP_ID_12244915 RMVar_hsa_circ_2789,RMVar_hsa_circ_335904,RMVar_hsa_circ_317370,RMVar_hsa_circ_127695,RMVar_hsa_circ_19524,RMVar_hsa_circ_164163,RMVar_hsa_circ_164164,RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_13291,RMVar_hsa_circ_164176,RMVar_hsa_circ_71756,RMVar_hsa_circ_164178,RMVar_hsa_circ_341500,RMVar_hsa_circ_351932,RMVar_hsa_circ_340667,RMVar_hsa_circ_324538,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_51059,RMVar_hsa_circ_164185,RMVar_hsa_circ_164186,RMVar_hsa_circ_164188,RMVar_hsa_circ_105805,RMVar_hsa_circ_368361,RMVar_hsa_circ_164189,RMVar_hsa_circ_281967,RMVar_hsa_circ_279785,RMVar_hsa_circ_7299,RMVar_hsa_circ_164190,RMVar_hsa_circ_33570,RMVar_hsa_circ_164194,RMVar_hsa_circ_332069,RMVar_hsa_circ_50837,RMVar_hsa_circ_164193,RMVar_hsa_circ_42703,RMVar_hsa_circ_71035,RMVar_hsa_circ_124797,RMVar_hsa_circ_111503,RMVar_hsa_circ_164195,RMVar_hsa_circ_164196 115220 RMVar_ID_115220 Human_SNP_ID_817950639 m1A Human chr13 - 110914826 110914826 110914826 TGCACCGCGCCTGCCGCGACGGGGACCTGGCCACGCTCTGCTCGCTGCTGCAGCAGACACCCCAC TGCACCGCGCCTGCCGCGACGGGGACCTGGCCGCGCTCTGCTCGCTGCTGCAGCAGACACCCCAC T C ANKRD10 Ensembl:ENSG00000088448 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr13:110914690..110915082;chr13:110914776..110915050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_879588,Human_RBP_ID_4277532,Human_RBP_ID_6258016,Human_RBP_ID_22426181,Human_RBP_ID_22795821 Human_miRNA_ID_2756752 RMVar_hsa_circ_119664,RMVar_hsa_circ_164778 115221 RMVar_ID_115221 Human_SNP_ID_817967648 m1A Human chr13 + 27945464 27945464 27945464 CTTGAAATGCTGCATTTCCAAGGTGAAGATGTATGGGCACATGTTATGGCAGATTGAAAAGGATC CTTGAAATGCTGCATTTCCAAGGTGAAGATGTGTGGGCACATGTTATGGCAGATTGAAAAGGATC A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs771065359 Functional Loss SNV ICGC 33..33 33 LAML 2 - 115222 RMVar_ID_115222 Human_SNP_ID_818036978 m1A Human chr13 - 95641747 95641747 95641747 CGGGTGCGGCCTCCATGGCCTGTGCGCCCCCCAGCGCGGCTTCGGGGCCCCTGCCCTTCTTCCAG CGGGTGCGGCCTCCATGGCCTGTGCGCCCCCCGGCGCGGCTTCGGGGCCCCTGCCCTTCTTCCAG T C DZIP1 Ensembl:ENSG00000134874 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:95641740..95641891 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_440507,Human_RBP_ID_5462998 RMVar_hsa_circ_266932,RMVar_hsa_circ_41962,RMVar_hsa_circ_5337,RMVar_hsa_circ_31348,RMVar_hsa_circ_32667,RMVar_hsa_circ_274637,RMVar_hsa_circ_164144,RMVar_hsa_circ_164145,RMVar_hsa_circ_312970,RMVar_hsa_circ_334336 115223 RMVar_ID_115223 Human_SNP_ID_818048355 m1A Human chr13 - 33818212 33818212 33818212 CTGCTCCTTGTGATAGTCCAGCCGTCCCAAGGAGCAGGGCCGATACTTGTCCACCCAGAGGCTCA CTGCTCCTTGTGATAGTCCAGCCGTCCCAAGGTGCAGGGCCGATACTTGTCCACCCAGAGGCTCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:33818119..33818300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney renal_cell_carcinoma_unclassified 2 kidney 115224 RMVar_ID_115224 Human_SNP_ID_818069701 m1A Human chr13 + 110506527 110506527 110506527 CACAGCCAGACGGACCAGGAGCCCATGTGCCCAGTGGGCATGAACAAACTCTGGAGTGGATACAG CACAGCCAGACGGACCAGGAGCCCATGTGCCCGGTGGGCATGAACAAACTCTGGAGTGGATACAG A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs445348 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_17685921 Human_Splice_Rec_1482817,Human_Splice_Rec_1482919,Human_Splice_Rec_1482933,Human_Splice_Rec_1482941 Clinvar_Rec_230 GWAS_ID_7668,GWAS_ID_7669,GWAS_ID_7670,GWAS_ID_7671,GWAS_ID_7672,GWAS_ID_7673,GWAS_ID_7674 RMVar_hsa_circ_109237,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_91490,RMVar_hsa_circ_164726,RMVar_hsa_circ_106872,RMVar_hsa_circ_164727,RMVar_hsa_circ_114020,RMVar_hsa_circ_164735,RMVar_hsa_circ_164736,RMVar_hsa_circ_104928,RMVar_hsa_circ_115927,RMVar_hsa_circ_126421,RMVar_hsa_circ_164739,RMVar_hsa_circ_164740 115225 RMVar_ID_115225 Human_SNP_ID_818077625 m1A Human chr13 - 49533153 49533153 49533153 AAGAAGTGGTTCTTCAAGTCAACCCTCTTACAAGACTTAGTGGAATTTGCTTTATCTACTTTAGG AAGAAGTGGTTCTTCAAGTCAACCCTCTTACAGGACTTAGTGGAATTTGCTTTATCTACTTTAGG T C RCBTB1 Ensembl:ENSG00000136144 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1046028 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_23598631,Human_RBP_ID_27640236 GWAS_ID_14095,GWAS_ID_14096,GWAS_ID_14097,GWAS_ID_14098,GWAS_ID_14099,GWAS_ID_14100,GWAS_ID_14101,GWAS_ID_14102,GWAS_ID_14103,GWAS_ID_14104,GWAS_ID_14105,GWAS_ID_14106,GWAS_ID_14107,GWAS_ID_14108,GWAS_ID_14109,GWAS_ID_14110,GWAS_ID_14111,GWAS_ID_14112,GWAS_ID_14113,GWAS_ID_14114,GWAS_ID_14115,GWAS_ID_14116,GWAS_ID_14117,GWAS_ID_14118,GWAS_ID_14119,GWAS_ID_14120,GWAS_ID_14121,GWAS_ID_14122,GWAS_ID_14123,GWAS_ID_14124,GWAS_ID_14125,GWAS_ID_14126,GWAS_ID_14127,GWAS_ID_14128,GWAS_ID_14129,GWAS_ID_14130,GWAS_ID_14131,GWAS_ID_14132,GWAS_ID_14133,GWAS_ID_14134,GWAS_ID_14135,GWAS_ID_14136,GWAS_ID_14137,GWAS_ID_14138,GWAS_ID_14139,GWAS_ID_14140,GWAS_ID_14141,GWAS_ID_14142,GWAS_ID_14143,GWAS_ID_14144,GWAS_ID_14145,GWAS_ID_14146,GWAS_ID_14147,GWAS_ID_14148,GWAS_ID_14149,GWAS_ID_14150,GWAS_ID_14151,GWAS_ID_14152,GWAS_ID_14153,GWAS_ID_14154,GWAS_ID_14155,GWAS_ID_14156,GWAS_ID_14157,GWAS_ID_14158,GWAS_ID_14159,GWAS_ID_14160,GWAS_ID_14161,GWAS_ID_14162,GWAS_ID_14163,GWAS_ID_14164,GWAS_ID_14165,GWAS_ID_14166,GWAS_ID_14167,GWAS_ID_14168,GWAS_ID_14169,GWAS_ID_14170,GWAS_ID_14171,GWAS_ID_14172,GWAS_ID_14173,GWAS_ID_14174,GWAS_ID_14175,GWAS_ID_14176 RMVar_hsa_circ_94516,RMVar_hsa_circ_163392 115226 RMVar_ID_115226 Human_SNP_ID_818101785 m1A Human chr13 + 27171669 27171669 27171669 CATCCGGCCAGCGCCATCTTCCACCCAATCACAGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCC CATCCGGCCAGCGCCATCTTCCACCCAATCACGGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCC A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:27171621..27171783 26863196 MeRIP-seq:(Medium) rs974869903 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 115227 RMVar_ID_115227 Human_SNP_ID_818124757 m1A Human chr13 + 19633772 19633771 19633773 GCTGCTAGGATGGAGCAGGTTGCGGAGGGAGCAAGGGTGACCGCAGTCCCTGTGTCAGCTGCCGA GCTGCTAGGATGGAGCAGGTTGCGGAGGGAGC__GGGTGACCGCAGTCCCTGTGTCAGCTGCCGA CAA C MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:19633673..19633960 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 CESC 1 - Human_RBP_ID_4264769,Human_RBP_ID_9323588,Human_RBP_ID_9367320,Human_RBP_ID_18417758,Human_RBP_ID_18637339,Human_RBP_ID_22041956,Human_RBP_ID_26323973,Human_RBP_ID_27807558 RMVar_hsa_circ_161943,RMVar_hsa_circ_111206 115228 RMVar_ID_115228 Human_SNP_ID_818221788 m1A Human chr13 + 110458853 110458853 110458853 CTTCCGGGACTGCCAGGACCCAAGGGCTTCGCAGGCATCAACGGGGAGCCGGGGAGGAAAGGGGA CTTCCGGGACTGCCAGGACCCAAGGGCTTCGCGGGCATCAACGGGGAGCCGGGGAGGAAAGGGGA A G COL4A2 Ensembl:ENSG00000134871 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:110458735..110458960 26863196 MeRIP-seq:(Medium) rs765359924 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_Splice_Rec_1482768,Human_Splice_Rec_1482769,Human_Splice_Rec_1482878 RMVar_hsa_circ_88497,RMVar_hsa_circ_109237,RMVar_hsa_circ_164716,RMVar_hsa_circ_164717,RMVar_hsa_circ_91432,RMVar_hsa_circ_164718,RMVar_hsa_circ_99086,RMVar_hsa_circ_164719,RMVar_hsa_circ_119483,RMVar_hsa_circ_164721,RMVar_hsa_circ_100470,RMVar_hsa_circ_164722,RMVar_hsa_circ_91490,RMVar_hsa_circ_107010,RMVar_hsa_circ_100011,RMVar_hsa_circ_77112,RMVar_hsa_circ_164723,RMVar_hsa_circ_164725,RMVar_hsa_circ_18860,RMVar_hsa_circ_164726,RMVar_hsa_circ_164724,RMVar_hsa_circ_106872,RMVar_hsa_circ_112586,RMVar_hsa_circ_89062,RMVar_hsa_circ_15349,RMVar_hsa_circ_164727,RMVar_hsa_circ_164729,RMVar_hsa_circ_83337,RMVar_hsa_circ_164730,RMVar_hsa_circ_164728,RMVar_hsa_circ_96552,RMVar_hsa_circ_164732,RMVar_hsa_circ_119753,RMVar_hsa_circ_16608,RMVar_hsa_circ_359949,RMVar_hsa_circ_164733 115229 RMVar_ID_115229 Human_SNP_ID_818324999 m1A Human chr13 - 25251751 25251751 25251751 TCATAAAGGTTTTGGAGGAACATGTACCATCAATTTGATCGAACACTGCATCCTAGGCAGTCTGT TCATAAAGGTTTTGGAGGAACATGTACCATCAGTTTGATCGAACACTGCATCCTAGGCAGTCTGT T C MTMR6 Ensembl:ENSG00000139505 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4312169 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA 6 stomach Human_RBP_ID_23589099 Human_Splice_Rec_1451594 GWAS_ID_9294,GWAS_ID_9295,GWAS_ID_9296,GWAS_ID_9297,GWAS_ID_9298,GWAS_ID_9299 RMVar_hsa_circ_17934,RMVar_hsa_circ_284668,RMVar_hsa_circ_55478,RMVar_hsa_circ_162288 115230 RMVar_ID_115230 Human_SNP_ID_818342974 m1A Human chr13 + 91348947 91348947 91348947 GCCGGGCTCGGGGGGGCTGGGGGACACAAAGGAGGGGCGGCGCGCCCGCGTCCCCGCCGCACTCG GCCGGGCTCGGGGGGGCTGGGGGACACAAAGGGGGGGCGGCGCGCCCGCGTCCCCGCCGCACTCG A G MIR17HG Ensembl:ENSG00000215417 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:91348923..91349346 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3997,Human_RBP_ID_260370,Human_RBP_ID_3438777,Human_RBP_ID_5087546,Human_RBP_ID_5140490,Human_RBP_ID_5174411,Human_RBP_ID_5351130,Human_RBP_ID_5645471,Human_RBP_ID_8075118,Human_RBP_ID_8180115,Human_RBP_ID_8230254,Human_RBP_ID_8725600,Human_RBP_ID_8792007,Human_RBP_ID_9281304,Human_RBP_ID_9323499,Human_RBP_ID_9417183,Human_RBP_ID_17114797,Human_RBP_ID_17360773,Human_RBP_ID_18189328,Human_RBP_ID_18417875,Human_RBP_ID_18480251,Human_RBP_ID_21968544,Human_RBP_ID_22369948,Human_RBP_ID_22426175,Human_RBP_ID_22472593,Human_RBP_ID_22710668,Human_RBP_ID_26768524,Human_RBP_ID_26777795 115231 RMVar_ID_115231 Human_SNP_ID_818387247 m1A Human chr13 - 99373605 99373605 99373605 TGACGGCCTTTCTTGGCCTCAGCAGCACCCGAACACTTCCACAAGCTCTTTGTCCACCTGTTTCC TGACGGCCTTTCTTGGCCTCAGCAGCACCCGACCACTTCCACAAGCTCTTTGTCCACCTGTTTCC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:99373567..99373799 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115232 RMVar_ID_115232 Human_SNP_ID_818411233 m1A Human chr13 + 113076105 113076105 113076105 TTTGGAGACCGGTGCGGAAAATAAGATCCAGGAGCTCAACGCGATTTACAAGGAATACGAATCCA TTTGGAGACCGGTGCGGAAAATAAGATCCAGGTGCTCAACGCGATTTACAAGGAATACGAATCCA A T MCF2L Ensembl:ENSG00000126217 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113076054..113076202 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 14 liver Human_RBP_ID_5561063,Human_RBP_ID_9368167,Human_RBP_ID_26324528 Human_Splice_Rec_1484501,Human_Splice_Rec_1484563,Human_Splice_Rec_1484617,Human_Splice_Rec_1484675,Human_Splice_Rec_1484743,Human_Splice_Rec_1484801,Human_Splice_Rec_1484887 RMVar_hsa_circ_66279,RMVar_hsa_circ_77256,RMVar_hsa_circ_164876,RMVar_hsa_circ_378589 115233 RMVar_ID_115233 Human_SNP_ID_818462185 m1A Human chr13 - 46553537 46553537 46553537 GGCAGGTTGAAGCCCCCGCTGCCACCGCCGCCACCACCCGCCCCGCCGGGGGCGCCGGTTCCTCC GGCAGGTTGAAGCCCCCGCTGCCACCGCCGCCGCCACCCGCCCCGCCGGGGGCGCCGGTTCCTCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:46553493..46553582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115234 RMVar_ID_115234 Human_SNP_ID_818479993 m1A Human chr13 - 109782224 109782224 109782224 CCAGCCGCAGCCGCCGCCGCCGCCGCTTCCTCAGCCGGGAGACAAGAGCTCCTGGGGCCGGACCC CCAGCCGCAGCCGCCGCCGCCGCCGCTTCCTCGGCCGGGAGACAAGAGCTCCTGGGGCCGGACCC T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109782176..109782250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 115235 RMVar_ID_115235 Human_SNP_ID_818491467 m1A Human chr13 - 22897990 22897990 22897990 CAGAGCCAAACTCCAAGATGACAGGCAAACTCAGCAAGAAGAAGGGCTACAATGTGAACGACGAG CAGAGCCAAACTCCAAGATGACAGGCAAACTCTGCAAGAAGAAGGGCTACAATGTGAACGACGAG T A BASP1P1,LINC00621 Ensembl:ENSG00000230535,Ensembl:ENSG00000262619 Pseudogene,lincRNA exon,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:22897909..22898012 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115236 RMVar_ID_115236 Human_SNP_ID_818498659 m1A Human chr13 + 45516235 45516235 45516235 GCTCCATTTCACACTGAATTCACCATTAAGGAAATTTCCCTGGACCTCAAGAAAACTAGAGGTAC GCTCCATTTCACACTGAATTCACCATTAAGGACATTTCCCTGGACCTCAAGAAAACTAGAGGTAC A C COG3 Ensembl:ENSG00000136152 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_9367484 Human_Splice_Rec_1462072,Human_Splice_Rec_1462073,Human_Splice_Rec_1462121 Human_miRNA_ID_2865808 RMVar_hsa_circ_34300,RMVar_hsa_circ_355674,RMVar_hsa_circ_64321,RMVar_hsa_circ_88620,RMVar_hsa_circ_84243,RMVar_hsa_circ_163205,RMVar_hsa_circ_163206,RMVar_hsa_circ_57372,RMVar_hsa_circ_93417,RMVar_hsa_circ_78221,RMVar_hsa_circ_37247,RMVar_hsa_circ_163210,RMVar_hsa_circ_163209,RMVar_hsa_circ_31649,RMVar_hsa_circ_268577,RMVar_hsa_circ_372022,RMVar_hsa_circ_64536,RMVar_hsa_circ_34821,RMVar_hsa_circ_163211,RMVar_hsa_circ_59967,RMVar_hsa_circ_35785,RMVar_hsa_circ_4848,RMVar_hsa_circ_343034,RMVar_hsa_circ_163212,RMVar_hsa_circ_163216,RMVar_hsa_circ_163220,RMVar_hsa_circ_278719,RMVar_hsa_circ_282217,RMVar_hsa_circ_283326,RMVar_hsa_circ_276408,RMVar_hsa_circ_163218,RMVar_hsa_circ_163219,RMVar_hsa_circ_163217 115237 RMVar_ID_115237 Human_SNP_ID_818504800 m1A Human chr13 + 50092049 50092048 50092049 CACTAAATAGGTGGTAGTTCAGATTATGAGGGAAATGGATGCCATTGCTCATAGAGACTAAACAT CACTAAATAGGTGGTAGTTCAGATTATGAGGG_AATGGATGCCATTGCTCATAGAGACTAAACAT GA G DLEU1 Ensembl:ENSG00000176124 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:50092045..50092250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_12182281 RMVar_hsa_circ_123422,RMVar_hsa_circ_163444 115238 RMVar_ID_115238 Human_SNP_ID_818548419 m1A Human chr13 - 20975144 20975144 20975144 CCCCTACGTTCCCACCATCAGCCACCCCATGGACACCTCGAATTTCGACCCCGTAGATGAAGAAA CCCCTACGTTCCCACCATCAGCCACCCCATGGGCACCTCGAATTTCGACCCCGTAGATGAAGAAA T C LATS2 Ensembl:ENSG00000150457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:20975044..20975225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_27426942 RMVar_hsa_circ_162131,RMVar_hsa_circ_80750,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132 115239 RMVar_ID_115239 Human_SNP_ID_818567125 m1A Human chr13 + 109765539 109765539 109765539 AGCATGTAGATATCCCAGCCTCAACCACCCTGACTCCAACTCCCCACCAAGCATGTAGATATCCC AGCATGTAGATATCCCAGCCTCAACCACCCTGGCTCCAACTCCCCACCAAGCATGTAGATATCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:109765534..109765620 26863196 MeRIP-seq:(Medium) rs4773085 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 115240 RMVar_ID_115240 Human_SNP_ID_818569481 m1A Human chr13 - 45969635 45969635 45969635 AGCAAAAATTCAAAAGAAACCAATTAAGAAAAAGAAAGAGGATGATGTTGGAATAGAGAGGGGTA AGCAAAAATTCAAAAGAAACCAATTAAGAAAACGAAAGAGGATGATGTTGGAATAGAGAGGGGTA T G ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:45969383..45969683 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 4 uterus Human_RBP_ID_23597339 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 115241 RMVar_ID_115241 Human_SNP_ID_818569501 m1A Human chr13 - 45969635 45969635 45969635 AGCAAAAATTCAAAAGAAACCAATTAAGAAAAAGAAAGAGGATGATGTTGGAATAGAGAGGGGTA AGCAAAAATTCAAAAGAAACCAATTAAGAAAAGGAAAGAGGATGATGTTGGAATAGAGAGGGGTA T C ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:45969383..45969683 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_23597339 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_360309,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163223,RMVar_hsa_circ_266192,RMVar_hsa_circ_266229,RMVar_hsa_circ_71037,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941 115242 RMVar_ID_115242 Human_SNP_ID_818698351 m1A Human chr13 - 113599874 113599874 113599874 CAAGGATTCTCTCTGGCAGTCCTGAAGCCCTAAGCACAAGGGTTCTCTTTCACGGTCCTGGGTTC CAAGGATTCTCTCTGGCAGTCCTGAAGCCCTAGGCACAAGGGTTCTCTTTCACGGTCCTGGGTTC T C lnc-ATP4B-1,lnc-ATP4B-1:2 RNACentral:URS00008BF973,RNACentral:URS00008B5C69 lincRNA,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr13:113599866..113600015 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115243 RMVar_ID_115243 Human_SNP_ID_818743897 m1A Human chr13 + 49691416 49691416 49691416 GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCAGCGCCCATGCTTCAGGCTTCCGACGCCAACGG GAACCGCCAGCCTCGGCCCCCAGCTCCCACTCGGCGCCCATGCTTCAGGCTTCCGACGCCAACGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr13:49691251..49691475;chr13:49669838..49691475 26863196 MeRIP-seq:(Medium) rs911699272 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung 115244 RMVar_ID_115244 Human_SNP_ID_818744234 m1A Human chr13 - 49534116 49534116 49534116 AGTAAATGTGGAGCCTTTAAGAACTGAAGCGCAAGGCTGCTGGGTTCTGTGTGAGTGCTCTGGGG AGTAAATGTGGAGCCTTTAAGAACTGAAGCGCGAGGCTGCTGGGTTCTGTGTGAGTGCTCTGGGG T C RCBTB1 Ensembl:ENSG00000136144 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7317982 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_miRNA_ID_2450628,Human_miRNA_ID_2540070 GWAS_ID_14177,GWAS_ID_14178,GWAS_ID_14179,GWAS_ID_14180,GWAS_ID_14181,GWAS_ID_14182,GWAS_ID_14183,GWAS_ID_14184,GWAS_ID_14185,GWAS_ID_14186,GWAS_ID_14187,GWAS_ID_14188,GWAS_ID_14189,GWAS_ID_14190,GWAS_ID_14191,GWAS_ID_14192,GWAS_ID_14193,GWAS_ID_14194,GWAS_ID_14195,GWAS_ID_14196,GWAS_ID_14197,GWAS_ID_14198,GWAS_ID_14199,GWAS_ID_14200,GWAS_ID_14201,GWAS_ID_14202,GWAS_ID_14203,GWAS_ID_14204,GWAS_ID_14205,GWAS_ID_14206,GWAS_ID_14207,GWAS_ID_14208,GWAS_ID_14209,GWAS_ID_14210,GWAS_ID_14211,GWAS_ID_14212,GWAS_ID_14213,GWAS_ID_14214,GWAS_ID_14215,GWAS_ID_14216,GWAS_ID_14217,GWAS_ID_14218,GWAS_ID_14219,GWAS_ID_14220,GWAS_ID_14221,GWAS_ID_14222,GWAS_ID_14223,GWAS_ID_14224,GWAS_ID_14225,GWAS_ID_14226,GWAS_ID_14227,GWAS_ID_14228,GWAS_ID_14229,GWAS_ID_14230,GWAS_ID_14231,GWAS_ID_14232,GWAS_ID_14233,GWAS_ID_14234,GWAS_ID_14235,GWAS_ID_14236,GWAS_ID_14237,GWAS_ID_14238,GWAS_ID_14239,GWAS_ID_14240,GWAS_ID_14241,GWAS_ID_14242,GWAS_ID_14243,GWAS_ID_14244,GWAS_ID_14245,GWAS_ID_14246,GWAS_ID_14247,GWAS_ID_14248,GWAS_ID_14249,GWAS_ID_14250,GWAS_ID_14251,GWAS_ID_14252,GWAS_ID_14253,GWAS_ID_14254,GWAS_ID_14255,GWAS_ID_14256,GWAS_ID_14257,GWAS_ID_14258 RMVar_hsa_circ_94516,RMVar_hsa_circ_163392 115245 RMVar_ID_115245 Human_SNP_ID_818748254 m1A Human chr13 - 45341123 45341123 45341123 AGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGAGTTTCAGGCTCGTGCTAAGCTAGCGCCGTCGT AGCGCCGCTCCGGCTGCACCGCGCTCGCTCCGGGTTTCAGGCTCGTGCTAAGCTAGCGCCGTCGT T C TPT1 Ensembl:ENSG00000133112 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr13:45340681..45341200;chr13:45340666..45341200;chr13:45341040..45341175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung Human_RBP_ID_230620,Human_RBP_ID_436571,Human_RBP_ID_1484546,Human_RBP_ID_3430648,Human_RBP_ID_4270846,Human_RBP_ID_5417714,Human_RBP_ID_5462793,Human_RBP_ID_5492746,Human_RBP_ID_8392607,Human_RBP_ID_12166584,Human_RBP_ID_18189317,Human_RBP_ID_22494666,Human_RBP_ID_23126300,Human_RBP_ID_26807469,Human_RBP_ID_27428018 Human_Splice_Rec_1461195,Human_Splice_Rec_1461205,Human_Splice_Rec_1461215,Human_Splice_Rec_1461245,Human_Splice_Rec_1461253,Human_Splice_Rec_1461271,Human_Splice_Rec_1461279,Human_Splice_Rec_1461287 RMVar_hsa_circ_121231,RMVar_hsa_circ_163175,RMVar_hsa_circ_60043 115246 RMVar_ID_115246 Human_SNP_ID_818763085 m1A Human chr13 - 46127236 46127236 46127236 TTAATTTTGATATAATCTTTCAAACCAGCTTCATGTGGCTTCCCTTTTCTTTGTTCAAGATGAGG TTAATTTTGATATAATCTTTCAAACCAGCTTCTTGTGGCTTCCCTTTTCTTTGTTCAAGATGAGG T A LCP1 Ensembl:ENSG00000136167 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1409429 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_996622,Human_RBP_ID_4271224,Human_RBP_ID_5112232,Human_RBP_ID_6287284,Human_RBP_ID_17476823,Human_RBP_ID_17838753,Human_RBP_ID_18268918 Human_miRNA_ID_433522,Human_miRNA_ID_3004278 GWAS_ID_14093,GWAS_ID_14094 RMVar_hsa_circ_125053,RMVar_hsa_circ_163247 115247 RMVar_ID_115247 Human_SNP_ID_818766096 m1A Human chr13 - 109765936 109765936 109765936 AGGCTGGGATATCTACATGCTTGGTGGGGAGGAGGAGCCAAGGTGGATGAGGCTGGGATATCTAC AGGCTGGGATATCTACATGCTTGGTGGGGAGGCGGAGCCAAGGTGGATGAGGCTGGGATATCTAC T G IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr13:109765891..109765984;chr13:109765906..109766138 26863196 MeRIP-seq:(Medium) rs1289749177 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,BRCA,breast ductal_carcinoma 3 prostate,breast RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 115248 RMVar_ID_115248 Human_SNP_ID_818769108 m1A Human chr13 - 113520706 113520706 113520706 TTTACCTAGAAGATGCACTGGCGCCCGCCTGTATGAGAGTCGGCATGACGGCCATGAAGAGCCCG TTTACCTAGAAGATGCACTGGCGCCCGCCTGTGTGAGAGTCGGCATGACGGCCATGAAGAGCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113520601..113520750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 115249 RMVar_ID_115249 Human_SNP_ID_818823542 m1A Human chr13 + 20718482 20718482 20718482 TCACACACCCACACACACCTGCCCACGCTCACACCTGCCCCCACACACCTGCCCACACTCAGACA TCACACACCCACACACACCTGCCCACGCTCACCCCTGCCCCCACACACCTGCCCACACTCAGACA A C IL17D Ensembl:ENSG00000172458 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:20718310..20718482 26863196 MeRIP-seq:(Medium) rs1365858262 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115250 RMVar_ID_115250 Human_SNP_ID_818825282 m1A Human chr13 + 98519401 98519385 98519401 CACTTTCTGAGTCCGATTGTCAATGCCTTTGAACACCTCTCCAAAGGAGCCCTTCCCAATTTTCT CACTTTCTGAGTCCGAT________________CACCTCTCCAAAGGAGCCCTTCCCAATTTTCT TTGTCAATGCCTTTGAA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:98519351..98519425 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 18..33 33 SARC 1 - 115251 RMVar_ID_115251 Human_SNP_ID_818909941 m1A Human chr13 + 109783112 109783112 109783112 CCGGCTTAGGAGACTTGGGGGAGCTGAAGTCGAGGTTCATGTAGTCGGAGAGCGGAGACCGCTGC CCGGCTTAGGAGACTTGGGGGAGCTGAAGTCGTGGTTCATGTAGTCGGAGAGCGGAGACCGCTGC A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:109782501..109783275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 115252 RMVar_ID_115252 Human_SNP_ID_818928637 m1A Human chr13 + 73062122 73062122 73062122 AACCTGTTGCCATTTTCAGCCACCAGAGTGAAACGACTGCCCCTCCTCCGGCCCCGACCCAGGCC AACCTGTTGCCATTTTCAGCCACCAGAGTGAAGCGACTGCCCCTCCTCCGGCCCCGACCCAGGCC A G KLF5 Ensembl:ENSG00000102554 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:73062073..73062178 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_25063319 115253 RMVar_ID_115253 Human_SNP_ID_818982080 m1A Human chr13 - 110719579 110719579 110719579 CGAGGCGCCGTCGTCGTGGTCGTGGTTGCTGGACGCGTTCTCACGGTTCTCGTTGTTGCGCTGCC CGAGGCGCCGTCGTCGTGGTCGTGGTTGCTGGGCGCGTTCTCACGGTTCTCGTTGTTGCGCTGCC T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110719451..110719719 26863196 MeRIP-seq:(Medium) rs1342833850 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 4 head and neck 115254 RMVar_ID_115254 Human_SNP_ID_818986341 m1A Human chr13 + 109784398 109784398 109784398 GCGTCCCCCGAGACCCGGCGGTAGGAGCGGCCACAGTGGCTCAGGGGCCTGTCCATGGTCATGTA GCGTCCCCCGAGACCCGGCGGTAGGAGCGGCCGCAGTGGCTCAGGGGCCTGTCCATGGTCATGTA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:109784348..109784453 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck 115255 RMVar_ID_115255 Human_SNP_ID_819019213 m1A Human chr13 + 59820976 59820976 59820976 CAACATATTATAATATCCTGTATATTTTTGCGACATAGAAAACTAGGAGATTTAATCATTTGAAA CAACATATTATAATATCCTGTATATTTTTGCGGCATAGAAAACTAGGAGATTTAATCATTTGAAA A G lnc-TDRD3-11 RNACentral:URS00008B92AC lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr13:59820925..59821057 26863196 MeRIP-seq:(Medium) rs1247913254 Functional Loss SNV ICGC 33..33 33 MALY 1 - 115256 RMVar_ID_115256 Human_SNP_ID_819020769 m1A Human chr13 - 51452805 51452805 51452805 GGAGCGGGGACGGGACCCCCGAGGCGGGGGGGACGAACCGACAGACAGACGGCTGGGCGCCCGCC GGAGCGGGGACGGGACCCCCGAGGCGGGGGGGGCGAACCGACAGACAGACGGCTGGGCGCCCGCC T C INTS6 Ensembl:ENSG00000102786 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:51452763..51452988 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_38292,Human_RBP_ID_756321,Human_RBP_ID_5315335,Human_RBP_ID_9323622,Human_RBP_ID_9417553,Human_RBP_ID_21968414 115257 RMVar_ID_115257 Human_SNP_ID_819030681 m1A Human chr13 + 113208532 113208532 113208532 GCGGGAAAGGAAAAGGCCTGAGGGTCCAAGGCAGGAGGGGACACACGGAACACGCCGAGGGCCAA GCGGGAAAGGAAAAGGCCTGAGGGTCCAAGGCGGGAGGGGACACACGGAACACGCCGAGGGCCAA A G CUL4A Ensembl:ENSG00000139842 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:113208482..113208639 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_Splice_Rec_1485459 115258 RMVar_ID_115258 Human_SNP_ID_819143976 m1A Human chr13 + 99985042 99985042 99985042 GAAGAAGCACATGCACGTCCACACCTCCGATAAGCCCTATCTCTGCAAGATGTGCGACAAGTCCT GAAGAAGCACATGCACGTCCACACCTCCGATATGCCCTATCTCTGCAAGATGTGCGACAAGTCCT A T ZIC2 Ensembl:ENSG00000043355 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:99984994..99985090 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_1804119,Human_RBP_ID_6253635,Human_RBP_ID_8788006,Human_RBP_ID_12092221,Human_RBP_ID_18635790 Human_Splice_Rec_1478506,Human_Splice_Rec_1478507,Human_Splice_Rec_1478510,Human_Splice_Rec_1478511,Human_Splice_Rec_1478514,Human_Splice_Rec_1478515,Human_Splice_Rec_1478517 115259 RMVar_ID_115259 Human_SNP_ID_819238104 m1A Human chr13 - 49247997 49247997 49247997 TAGCGTCCTCTGCTGCCAAGGAAACCTCTCCCAGTCAGACATGATCTCGGCCCTAGCGCCCCCGC TAGCGTCCTCTGCTGCCAAGGAAACCTCTCCCCGTCAGACATGATCTCGGCCCTAGCGCCCCCGC T G LOC105370203 RNACentral:URS0000D5941F lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:49247949..49248100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115260 RMVar_ID_115260 Human_SNP_ID_819254643 m1A Human chr13 + 76886279 76886279 76886279 CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCACCGCCGCCACCGCCACCGCCGCCACCTCCTAG CAGCCCTGCGCCCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCACCGCCGCCACCTCCTAG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK293T cell line,total RNA;HEK293T,untreat control;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr13:76886178..76886400;chr13:76886190..76886290;chr13:76885919..76886388;chr13:76886048..76886424;chr13:76886050..76886367 26863196,26863410,26863196,26863196,26863196 MeRIP-seq:(Medium) rs973803018 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 115261 RMVar_ID_115261 Human_SNP_ID_819351820 m1A Human chr13 + 112778745 112778745 112778745 GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCACTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG GGAGTGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGGAGTAGCCGCTGGAGTGAGTAG A G ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:112778520..112778799 26863196 MeRIP-seq:(Medium) rs61961155 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115262 RMVar_ID_115262 Human_SNP_ID_819486420 m1A Human chr13 + 75853333 75853333 75853333 CCACCACAGGTGTGGCCACCACACAGTCCCCCACCCCGAGAAGCCATTCCCCTTCAGCTTCACAG CCACCACAGGTGTGGCCACCACACAGTCCCCCCCCCCGAGAAGCCATTCCCCTTCAGCTTCACAG A C LMO7 Ensembl:ENSG00000136153 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr13:75853203..75853400 26863196 MeRIP-seq:(Medium) rs754898427 Functional Loss SNV ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 13 large intestine Human_RBP_ID_9367618,Human_RBP_ID_17245972 Human_Splice_Rec_1471959,Human_Splice_Rec_1472017,Human_Splice_Rec_1472139,Human_Splice_Rec_1472205,Human_Splice_Rec_1472265,Human_Splice_Rec_1472319,Human_Splice_Rec_1472445 RMVar_hsa_circ_114831,RMVar_hsa_circ_163788,RMVar_hsa_circ_53564,RMVar_hsa_circ_63058,RMVar_hsa_circ_53989,RMVar_hsa_circ_72473,RMVar_hsa_circ_265372,RMVar_hsa_circ_29053,RMVar_hsa_circ_38367 115263 RMVar_ID_115263 Human_SNP_ID_819502833 m1A Human chr13 - 109785975 109785975 109785975 ACGGCCCCAACCTCAACAACAACAACAACAACAACAACCACAGCGTGCGCAAGTGCGGCTACCTG ACGGCCCCAACCTCAACAACAACAACAACAACGACAACCACAGCGTGCGCAAGTGCGGCTACCTG T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:109785818..109786600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 115264 RMVar_ID_115264 Human_SNP_ID_819502934 m1A Human chr13 - 109785975 109785969 109785975 ACGGCCCCAACCTCAACAACAACAACAACAACAACAACCACAGCGTGCGCAAGTGCGGCTACCTG ACGGCCCCAACCTCAACAACAACAACAACAAC______CACAGCGTGCGCAAGTGCGGCTACCTG GGTTGTT G IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:109785818..109786600 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..38 33 PRAD 1 - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 115265 RMVar_ID_115265 Human_SNP_ID_819509824 m1A Human chr13 - 113490108 113490108 113490108 TGGCTGTAGGTGTGCATCTGTGGAGCTGGTAGAGTTCCGCAGCGCAGGAGGGAGGCTGCTGGAGG TGGCTGTAGGTGTGCATCTGTGGAGCTGGTAGTGTTCCGCAGCGCAGGAGGGAGGCTGCTGGAGG T A DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:113490085..113490185 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_118959,Human_RBP_ID_5351259,Human_RBP_ID_9323689 115266 RMVar_ID_115266 Human_SNP_ID_819541402 m1A Human chr13 - 76885563 76885563 76885563 GTCCGTCCGGGGGCGCGGCGGGCCCGCTGCTCACGCCGTCCCAGTCGCTGGACGGCAGCCGGCGC GTCCGTCCGGGGGCGCGGCGGGCCCGCTGCTCGCGCCGTCCCAGTCGCTGGACGGCAGCCGGCGC T C KCTD12 Ensembl:ENSG00000178695 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr13:76885462..76885743 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_4274065 115267 RMVar_ID_115267 Human_SNP_ID_819546834 m1A Human chr13 - 76884924 76884924 76884924 GAACCGAGAGAACCCAGAGGAACCCCCACCCCACCCCCACCTACCACTCCATGCTTTCTCTACTC GAACCGAGAGAACCCAGAGGAACCCCCACCCCCCCCCCACCTACCACTCCATGCTTTCTCTACTC T G KCTD12 Ensembl:ENSG00000178695 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs953550553 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_230729,Human_RBP_ID_439131,Human_RBP_ID_22181864,Human_RBP_ID_26426970,Human_RBP_ID_27222560 115268 RMVar_ID_115268 Human_SNP_ID_819601080 m1A Human chr13 - 109783421 109783421 109783421 TTCGCCCGTGCGGCCTAGCGGCGGCCGCCCGGAGGGCTTCTTGGGCCAGCGCGGCCGGGCGGTGA TTCGCCCGTGCGGCCTAGCGGCGGCCGCCCGGGGGGCTTCTTGGGCCAGCGCGGCCGGGCGGTGA T C IRS2 Ensembl:ENSG00000185950 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:109783401..109783425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 115269 RMVar_ID_115269 Human_SNP_ID_819608187 m1A Human chr13 + 113306523 113306522 113306523 TGCATTGTGCGTCAGCAGCAATGTTTATGGTGAAAAATGGCAACGGGACCGCGTGCATAATGGCC TGCATTGTGCGTCAGCAGCAATGTTTATGGTG_AAAATGGCAACGGGACCGCGTGCATAATGGCC GA G LAMP1 Ensembl:ENSG00000185896 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:113306476..113306550 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_1805289,Human_RBP_ID_4276529,Human_RBP_ID_8388256,Human_RBP_ID_17475577,Human_RBP_ID_19829811,Human_RBP_ID_22438365,Human_RBP_ID_22737312 Human_Splice_Rec_1485688,Human_Splice_Rec_1485689,Human_Splice_Rec_1485703 RMVar_hsa_circ_77204,RMVar_hsa_circ_87658,RMVar_hsa_circ_164911,RMVar_hsa_circ_164910,RMVar_hsa_circ_164912,RMVar_hsa_circ_279299,RMVar_hsa_circ_300709,RMVar_hsa_circ_371638,RMVar_hsa_circ_83132,RMVar_hsa_circ_164914,RMVar_hsa_circ_164916,RMVar_hsa_circ_164918,RMVar_hsa_circ_75946,RMVar_hsa_circ_164917,RMVar_hsa_circ_164915,RMVar_hsa_circ_164913 115270 RMVar_ID_115270 Human_SNP_ID_819701593 m1A Human chr13 + 49936275 49936275 49936275 GGACCACCGACTCCGCCGCCGTCCCTAGACCGAGGCGACACTGCCCCCCGCCGCTCAGCTCCGTC GGACCACCGACTCCGCCGCCGTCCCTAGACCGGGGCGACACTGCCCCCCGCCGCTCAGCTCCGTC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr13:49936170..49936305;chr13:49936126..49936440 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115271 RMVar_ID_115271 Human_SNP_ID_819728937 m1A Human chr13 + 114301844 114301844 114301844 GGATGACGGCAGGAGGCACAGAGCTCACCACGAGCCTGAACGGCTTTCCAGAAGGAGTGAGGATG GGATGACGGCAGGAGGCACAGAGCTCACCACGTGCCTGAACGGCTTTCCAGAAGGAGTGAGGATG A T UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:114301673..114301900;chr13:114301669..114301900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_432734,Human_RBP_ID_24543581,Human_RBP_ID_26324250 Human_Splice_Rec_1486815 115272 RMVar_ID_115272 Human_SNP_ID_819775062 m1A Human chr13 - 75481331 75481331 75481331 CCTCACCTACTTTGCCTACCTGATCAAGGCGCAGCCCGACGACCCCGAGTCGCAGATGGCCTGCC CCTCACCTACTTTGCCTACCTGATCAAGGCGCCGCCCGACGACCCCGAGTCGCAGATGGCCTGCC T G TBC1D4 Ensembl:ENSG00000136111 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:75481285..75481426 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 3 haematopoietic and lymphoid tissue Human_RBP_ID_27222484 115273 RMVar_ID_115273 Human_SNP_ID_819800252 m1A Human chr13 - 78659111 78659111 78659111 TTGGCGGGATTCTGAACGCTGCCATGGCTCAGACCGTGCAGAATGTTACATTGTCGCTCACTCTG TTGGCGGGATTCTGAACGCTGCCATGGCTCAGGCCGTGCAGAATGTTACATTGTCGCTCACTCTG T C OBI1 Ensembl:ENSG00000152193 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:78659000..78659116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 3 lung Human_RBP_ID_1486184,Human_RBP_ID_4276658,Human_RBP_ID_22182270,Human_RBP_ID_22796563,Human_RBP_ID_23605470 Human_Splice_Rec_1473783 Human_miRNA_ID_1163325,Human_miRNA_ID_1217344 115274 RMVar_ID_115274 Human_SNP_ID_819814159 m1A Human chr13 - 78614399 78614399 78614399 TGGTATGCCTATATAGGTCTTTAAAAATGGGTATGTATGCTGTTTAATGTGCACTGAACATTTTA TGGTATGCCTATATAGGTCTTTAAAAATGGGTTTGTATGCTGTTTAATGTGCACTGAACATTTTA T A OBI1 Ensembl:ENSG00000152193 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1044385 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_439515,Human_RBP_ID_1486149,Human_RBP_ID_1812478,Human_RBP_ID_8946812,Human_RBP_ID_12226381,Human_RBP_ID_23605325 Human_miRNA_ID_1072167,Human_miRNA_ID_1258550,Human_miRNA_ID_2986913 GWAS_ID_13158,GWAS_ID_13159,GWAS_ID_13160,GWAS_ID_13161,GWAS_ID_13162,GWAS_ID_13163,GWAS_ID_13164,GWAS_ID_13165,GWAS_ID_13166,GWAS_ID_13167,GWAS_ID_13168,GWAS_ID_13169,GWAS_ID_13170,GWAS_ID_13171,GWAS_ID_13172,GWAS_ID_13173,GWAS_ID_13174,GWAS_ID_13175,GWAS_ID_13176,GWAS_ID_13177,GWAS_ID_13178,GWAS_ID_13179,GWAS_ID_13180,GWAS_ID_13181,GWAS_ID_13182 RMVar_hsa_circ_163958,RMVar_hsa_circ_93754 115275 RMVar_ID_115275 Human_SNP_ID_819849344 m1A Human chr13 - 99970413 99970413 99970413 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGGCCGGCGGCGCCAAGCCCTGCTC T C ZIC5 Ensembl:ENSG00000139800 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEK293T cell line,total RNA;HEPG2 cell line,mRNA heat shock 4h chr13:99970312..99970662;chr13:99970149..99970440;chr13:99970382..99970495;chr13:99970253..99971161 26863196 MeRIP-seq:(Medium) rs1357567471 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_4261301 115276 RMVar_ID_115276 Human_SNP_ID_819903015 m1A Human chr13 + 49560078 49560078 49560078 GGCTATATCCATTGTGGCCCCAGGCATAAACCACTCCATCTGTGCACACAAAGCACACAAAAAAT GGCTATATCCATTGTGGCCCCAGGCATAAACCTCTCCATCTGTGCACACAAAGCACACAAAAAAT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:49559976..49566660 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 115277 RMVar_ID_115277 Human_SNP_ID_819927012 m1A Human chr13 - 110307201 110307201 110307201 TTTGAGGCGCCGCCCGCGCACCGCCGGGGGGGAGGGGGCAGCGCCAACAAATTGGGGAGCTCGGC TTTGAGGCGCCGCCCGCGCACCGCCGGGGGGGGGGGGGCAGCGCCAACAAATTGGGGAGCTCGGC T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr13:110307176..110307225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115278 RMVar_ID_115278 Human_SNP_ID_819933768 m1A Human chr13 + 27621953 27621953 27621953 GCGCTATGGGACAGAGCCCCCGATCCGCCAGCACCACCTGAGGATCCAGAAACCGCCCCAGCGAT GCGCTATGGGACAGAGCCCCCGATCCGCCAGCGCCACCTGAGGATCCAGAAACCGCCCCAGCGAT A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr13:27621851..27622072;chr13:27621851..27622143 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 12 uterus Human_RBP_ID_434150,Human_RBP_ID_1482359,Human_RBP_ID_4276574,Human_RBP_ID_8389816,Human_RBP_ID_18638339,Human_RBP_ID_26807675 Human_Splice_Rec_1452667,Human_Splice_Rec_1452671,Human_Splice_Rec_1452675,Human_Splice_Rec_1452679,Human_Splice_Rec_1452685,Human_Splice_Rec_1452687,Human_Splice_Rec_1452693,Human_Splice_Rec_1452699,Human_Splice_Rec_1452701 RMVar_hsa_circ_114835,RMVar_hsa_circ_162401 115279 RMVar_ID_115279 Human_SNP_ID_819944587 m1A Human chr13 + 75537566 75537566 75537566 GGGACGGCTGAAGGTCACCGGCTCGCGGACACAGGACTAGGGGAGACCTGGGGAAGGCTCAGGGT GGGACGGCTGAAGGTCACCGGCTCGCGGACACGGGACTAGGGGAGACCTGGGGAAGGCTCAGGGT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:75537520..75537655 26863196 MeRIP-seq:(Medium) rs9543964 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,COCA 6 prostate GWAS_ID_13156,GWAS_ID_13157 115280 RMVar_ID_115280 Human_SNP_ID_819997014 m1A Human chr13 + 27171690 27171690 27171690 CACCCAATCACAGCGGCGGCGGCGGGCGGGGGAGGAGGGGAGCCGGGCCGCCCGCTCGCACCGCA CACCCAATCACAGCGGCGGCGGCGGGCGGGGGGGGAGGGGAGCCGGGCCGCCCGCTCGCACCGCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr13:27171595..27171835;chr13:27171640..27171986 26863196 MeRIP-seq:(Medium) rs1020428001 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115281 RMVar_ID_115281 Human_SNP_ID_820144094 m1A Human chr13 + 112581821 112581821 112581821 TCACATAAATATCCCCAATCCAAATGTTTTATATACTTTTCAACTTTCTCATACCAAAAAGTTAG TCACATAAATATCCCCAATCCAAATGTTTTATGTACTTTTCAACTTTCTCATACCAAAAAGTTAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:112581819..112581924 26863196 MeRIP-seq:(Medium) rs756010770 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus 115282 RMVar_ID_115282 Human_SNP_ID_820165154 m1A Human chr13 + 36319616 36319616 36319616 GCATCTTATCAACCAAATTGTTTTGCCTTTCCACCCCATGGTGCCAAACCCATATACTCTCATAT GCATCTTATCAACCAAATTGTTTTGCCTTTCCCCCCCATGGTGCCAAACCCATATACTCTCATAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:36319607..36319723 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115283 RMVar_ID_115283 Human_SNP_ID_820186714 m1A Human chr13 - 51751417 51751417 51751417 CACAGGGCCCACCCCACCCTGCTGTGCCACCTACCTCCTGCCTCTCCACGTCCATGTTCCAGACG CACAGGGCCCACCCCACCCTGCTGTGCCACCTCCCTCCTGCCTCTCCACGTCCATGTTCCAGACG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:51751387..51751487 26863196 MeRIP-seq:(Medium) rs78760921 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115284 RMVar_ID_115284 Human_SNP_ID_820197771 m1A Human chr13 - 110429881 110429881 110429881 CCTTTCTGCCCTTTTGGTCCTTGGGGCCCCTAATTAGCAGATATATTGTAAAAAGAAAAAACAAC CCTTTCTGCCCTTTTGGTCCTTGGGGCCCCTATTTAGCAGATATATTGTAAAAAGAAAAAACAAC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr13:110429876..110429900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 115285 RMVar_ID_115285 Human_SNP_ID_820220344 m1A Human chr13 - 113355394 113355394 113355394 GGTGCTGAGTGGGGCCCAGGCGCAGATGGACCAGAATCCCGGCTACTACCACCAGCTTCTCCAGG GGTGCTGAGTGGGGCCCAGGCGCAGATGGACCCGAATCCCGGCTACTACCACCAGCTTCTCCAGG T G GRTP1 Ensembl:ENSG00000139835 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr13:113355308..113355505 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_9367773,Human_RBP_ID_26323965 Human_Splice_Rec_1485718,Human_Splice_Rec_1485719,Human_Splice_Rec_1485732,Human_Splice_Rec_1485733,Human_Splice_Rec_1485742,Human_Splice_Rec_1485743,Human_Splice_Rec_1485751 RMVar_hsa_circ_164931,RMVar_hsa_circ_284822,RMVar_hsa_circ_313492,RMVar_hsa_circ_164932,RMVar_hsa_circ_70767 115286 RMVar_ID_115286 Human_SNP_ID_820321295 m1A Human chr13 + 73062481 73062481 73062481 TGCACATACACAATGCCAAGTCAGTTTCTTCCACAACAGGCCACTTACTTTCCCCCGTCACCACC TGCACATACACAATGCCAAGTCAGTTTCTTCCGCAACAGGCCACTTACTTTCCCCCGTCACCACC A G KLF5 Ensembl:ENSG00000102554 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:73062431..73062549 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_38283 115287 RMVar_ID_115287 Human_SNP_ID_820339778 m1A Human chr13 + 111153990 111153990 111153990 CCTGCGCGGCTGCGGGGCTTCCCTGCGGCTGGAGGTGAGCGCGGGCGGCCACGGGCCGAGGGAGG CCTGCGCGGCTGCGGGGCTTCCCTGCGGCTGGTGGTGAGCGCGGGCGGCCACGGGCCGAGGGAGG A T ARHGEF7 Ensembl:ENSG00000102606 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr13:111153954..111154179;chr13:111153941..111154066 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_879909,Human_RBP_ID_18978995,Human_RBP_ID_19063050,Human_RBP_ID_23208396,Human_RBP_ID_24366990,Human_RBP_ID_27807801 Human_Splice_Rec_1483400,Human_Splice_Rec_1483402,Human_Splice_Rec_1483403,Human_Splice_Rec_1483472,Human_Splice_Rec_1483473,Human_Splice_Rec_1483518,Human_Splice_Rec_1483519,Human_Splice_Rec_1483560,Human_Splice_Rec_1483561,Human_Splice_Rec_1483570,Human_Splice_Rec_1483571,Human_Splice_Rec_1483600,Human_Splice_Rec_1483601,Human_Splice_Rec_1483623,Human_Splice_Rec_1483663 RMVar_hsa_circ_5360,RMVar_hsa_circ_53508,RMVar_hsa_circ_314409,RMVar_hsa_circ_348098,RMVar_hsa_circ_329608,RMVar_hsa_circ_119220,RMVar_hsa_circ_30691,RMVar_hsa_circ_164782,RMVar_hsa_circ_164783,RMVar_hsa_circ_164784 115288 RMVar_ID_115288 Human_SNP_ID_820344653 m1A Human chr13 + 114298969 114298969 114298969 GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCATGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG GTGCCCCCGGTGCAGTCGTAAAAGCCAGGCCCGTGGAAGGCTCGCTGGAGGAGCCCCAGGAGACG A G UPF3A Ensembl:ENSG00000169062 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114298926..114299025 26863196 MeRIP-seq:(Medium) rs3993409 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_22919914,Human_RBP_ID_24543580,Human_RBP_ID_26324248 Human_Splice_Rec_1486767,Human_Splice_Rec_1486785,Human_Splice_Rec_1486825,Human_Splice_Rec_1486839,Human_Splice_Rec_1486859 115289 RMVar_ID_115289 Human_SNP_ID_820356171 m1A Human chr13 + 114236858 114236858 114236858 CTCAGTGTCTTTACCTGACAGCACAATATCACAGAGCCGCCCATGCACTTCGGTCACGAAAACTG CTCAGTGTCTTTACCTGACAGCACAATATCACGGAGCCGCCCATGCACTTCGGTCACGAAAACTG A G CDC16 Ensembl:ENSG00000130177 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:114236714..114236875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - Human_RBP_ID_879267,Human_RBP_ID_1481523,Human_RBP_ID_1805559,Human_RBP_ID_5350763,Human_RBP_ID_12106995 Human_Splice_Rec_1486446,Human_Splice_Rec_1486447,Human_Splice_Rec_1486482,Human_Splice_Rec_1486483,Human_Splice_Rec_1486516,Human_Splice_Rec_1486517,Human_Splice_Rec_1486550,Human_Splice_Rec_1486551,Human_Splice_Rec_1486588,Human_Splice_Rec_1486589,Human_Splice_Rec_1486624,Human_Splice_Rec_1486625,Human_Splice_Rec_1486634,Human_Splice_Rec_1486635,Human_Splice_Rec_1486670,Human_Splice_Rec_1486671,Human_Splice_Rec_1486706,Human_Splice_Rec_1486707 Human_miRNA_ID_769580,Human_miRNA_ID_2806161,Human_miRNA_ID_2806162,Human_miRNA_ID_2809304,Human_miRNA_ID_2809305,Human_miRNA_ID_2812445,Human_miRNA_ID_2812446,Human_miRNA_ID_3069441,Human_miRNA_ID_3069442 RMVar_hsa_circ_8428,RMVar_hsa_circ_25038,RMVar_hsa_circ_315999,RMVar_hsa_circ_335960,RMVar_hsa_circ_343077,RMVar_hsa_circ_323738,RMVar_hsa_circ_289202,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_22296,RMVar_hsa_circ_165018,RMVar_hsa_circ_165019,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_300053,RMVar_hsa_circ_369628,RMVar_hsa_circ_374960,RMVar_hsa_circ_18138,RMVar_hsa_circ_165020,RMVar_hsa_circ_165021,RMVar_hsa_circ_165022,RMVar_hsa_circ_4374 115290 RMVar_ID_115290 Human_SNP_ID_820404612 m1A Human chr13 + 97434471 97434471 97434471 GCGGCGGCGGCGGCGGCGGCCGCGGAGGGACGATGCGCGAGTACAAAGTGGTGGTGCTGGGCTCG GCGGCGGCGGCGGCGGCGGCCGCGGAGGGACGCTGCGCGAGTACAAAGTGGTGGTGCTGGGCTCG A C RAP2A Ensembl:ENSG00000125249 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:97434196..97434620 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_230599,Human_RBP_ID_4276491,Human_RBP_ID_9323519,Human_RBP_ID_9352868,Human_RBP_ID_27223272 115291 RMVar_ID_115291 Human_SNP_ID_820414667 m1A Human chr13 - 52018914 52018913 52018914 AATGAGCCCAGGGAAGAATAATGAATAAAAAAACCTGAAATAAGAGGACAAAGTTGAGAATCAAT AATGAGCCCAGGGAAGAATAATGAATAAAAAA_CCTGAAATAAGAGGACAAAGTTGAGAATCAAT GT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:52018911..52019078 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 COAD,STAD 5 - 115292 RMVar_ID_115292 Human_SNP_ID_820424699 m1A Human chr13 + 72795504 72795504 72795504 TGCGTGACTTTGAGTTGACAGAAGAGCAATATATTAAATTAAAAGCTTTTCCTGAAGATCAGCTT TGCGTGACTTTGAGTTGACAGAAGAGCAATATGTTAAATTAAAAGCTTTTCCTGAAGATCAGCTT A G PIBF1 Ensembl:ENSG00000083535 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1372000 Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,COCA,skin basal_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 pancreas,skin,haematopoietic and lymphoid tissue Human_RBP_ID_3944284,Human_RBP_ID_22181605 Human_Splice_Rec_1471203,Human_Splice_Rec_1471235,Human_Splice_Rec_1471261 Human_miRNA_ID_150779,Human_miRNA_ID_1991845 GWAS_ID_6952,GWAS_ID_6953,GWAS_ID_6954,GWAS_ID_6955,GWAS_ID_6956,GWAS_ID_6957,GWAS_ID_6958,GWAS_ID_6959,GWAS_ID_6960 RMVar_hsa_circ_12798,RMVar_hsa_circ_163699,RMVar_hsa_circ_286083,RMVar_hsa_circ_372291,RMVar_hsa_circ_49229,RMVar_hsa_circ_117928,RMVar_hsa_circ_15768,RMVar_hsa_circ_163700,RMVar_hsa_circ_311174,RMVar_hsa_circ_378979,RMVar_hsa_circ_163698,RMVar_hsa_circ_349159,RMVar_hsa_circ_280471,RMVar_hsa_circ_70924,RMVar_hsa_circ_57135,RMVar_hsa_circ_163701,RMVar_hsa_circ_69026,RMVar_hsa_circ_370151,RMVar_hsa_circ_163703 115293 RMVar_ID_115293 Human_SNP_ID_820432807 m1A Human chr13 + 113838302 113838302 113838302 CACAGCCCAGCCCTGGAGCAGGGAGGGAGCCCAGAGGTGCACAGCCCAGCCCTGGAGCAGAGAGA CACAGCCCAGCCCTGGAGCAGGGAGGGAGCCCGGAGGTGCACAGCCCAGCCCTGGAGCAGAGAGA A G GAS6-AS1 Ensembl:ENSG00000233695 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113837924..113838563 26863196 MeRIP-seq:(Medium) rs1398935552 Functional Loss SNV COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,liver hepatocellular_carcinoma 3 ovary,liver 115294 RMVar_ID_115294 Human_SNP_ID_820452795 m1A Human chr13 + 110179320 110179320 110179320 CCAGGGGGTCCGATCGCTCCATGTTCTCCAGGAACGCCTGGTACCCCAATGCTCCCCTTCTCCCC CCAGGGGGTCCGATCGCTCCATGTTCTCCAGGGACGCCTGGTACCCCAATGCTCCCCTTCTCCCC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:110179236..110179354 26863196 MeRIP-seq:(Medium) rs192750030 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 115295 RMVar_ID_115295 Human_SNP_ID_820493665 m1A Human chr13 + 98021132 98021132 98021132 CAAACGTCTGGCCAATGTCGTTCGCCAAGTACAGGTAAGCTGATTTGGTTGAATTGGGGAGGGGG CAAACGTCTGGCCAATGTCGTTCGCCAAGTACGGGTAAGCTGATTTGGTTGAATTGGGGAGGGGG A G IPO5 Ensembl:ENSG00000065150 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr13:98021081..98021182 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_880104,Human_RBP_ID_19062944 Human_Splice_Rec_1476297,Human_Splice_Rec_1476351,Human_Splice_Rec_1476499,Human_Splice_Rec_1476571,Human_Splice_Rec_1476635,Human_Splice_Rec_1476675 RMVar_hsa_circ_358262,RMVar_hsa_circ_164280,RMVar_hsa_circ_101075,RMVar_hsa_circ_27575,RMVar_hsa_circ_347076 115296 RMVar_ID_115296 Human_SNP_ID_820554559 m1A Human chr13 - 45985633 45985633 45985633 AACCTCGAGATGGTCGGGATCGGAGAGATGCCAGAGATACTAGGGACCGAAGGGAACTAAGAGAC AACCTCGAGATGGTCGGGATCGGAGAGATGCCTGAGATACTAGGGACCGAAGGGAACTAAGAGAC T A ZC3H13 Ensembl:ENSG00000123200 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr13:45985585..45985751 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 4 lung Human_RBP_ID_230399,Human_RBP_ID_812487,Human_RBP_ID_4271125,Human_RBP_ID_6286761,Human_RBP_ID_8790424,Human_RBP_ID_9281230,Human_RBP_ID_9367496,Human_RBP_ID_12168206,Human_RBP_ID_17186957,Human_RBP_ID_24543559,Human_RBP_ID_26324087,Human_RBP_ID_27807935 Human_miRNA_ID_543459,Human_miRNA_ID_578694 RMVar_hsa_circ_64780,RMVar_hsa_circ_56054,RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_266192,RMVar_hsa_circ_269441,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_349924,RMVar_hsa_circ_354279,RMVar_hsa_circ_353025,RMVar_hsa_circ_364174,RMVar_hsa_circ_68147,RMVar_hsa_circ_365003,RMVar_hsa_circ_354213,RMVar_hsa_circ_327924,RMVar_hsa_circ_163226,RMVar_hsa_circ_80669,RMVar_hsa_circ_310612,RMVar_hsa_circ_351858,RMVar_hsa_circ_353296,RMVar_hsa_circ_368065,RMVar_hsa_circ_352367,RMVar_hsa_circ_340029,RMVar_hsa_circ_91037,RMVar_hsa_circ_163228,RMVar_hsa_circ_163229,RMVar_hsa_circ_163230,RMVar_hsa_circ_163227,RMVar_hsa_circ_163233,RMVar_hsa_circ_339229,RMVar_hsa_circ_355711,RMVar_hsa_circ_356519,RMVar_hsa_circ_361682,RMVar_hsa_circ_348215,RMVar_hsa_circ_299849,RMVar_hsa_circ_304505,RMVar_hsa_circ_163234,RMVar_hsa_circ_163231,RMVar_hsa_circ_163232 115297 RMVar_ID_115297 Human_SNP_ID_820566495 m1A Human chr13 + 113605955 113605955 113605955 AGGGGATCCTGTGGGAAGGCGGCGCGGTGGTGAGTGTCCGCAGGGGATCCTGTGGGAAGGCGGCG AGGGGATCCTGTGGGAAGGCGGCGCGGTGGTGTGTGTCCGCAGGGGATCCTGTGGGAAGGCGGCG A T TFDP1 Ensembl:ENSG00000198176 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr13:113605800..113606243 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_RBP_ID_8180312 RMVar_hsa_circ_45110,RMVar_hsa_circ_102960,RMVar_hsa_circ_164973 115298 RMVar_ID_115298 Human_SNP_ID_820580731 m1A Human chr13 - 99073349 99073346 99073349 GAGAGAGAGAGGAGAGAGAGAAAAGAAGAAGAAGAGAGGAGAGAAAGAAGAGAGAGAAGAGAGAG GAGAGAGAGAGGAGAGAGAGAAAAGAAGAAGA___GAGGAGAGAAAGAAGAGAGAGAAGAGAGAG CTCT C DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr13:99073342..99073426 26863196 MeRIP-seq:(Medium) rs765715965 Functional Loss DEL ICGC 33..35 33 LICA 1 - Human_RBP_ID_25081387 115299 RMVar_ID_115299 Human_SNP_ID_820699804 m1A Human chr13 + 19958804 19958804 19958804 GTGCGTGTCGCCGAAGGGGGGTGGGCCGGGGGAGGGGAGGTTCGTTCCGCGGAGCCCCAGCCAGA GTGCGTGTCGCCGAAGGGGGGTGGGCCGGGGGGGGGGAGGTTCGTTCCGCGGAGCCCCAGCCAGA A G ZMYM2 Ensembl:ENSG00000121741 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr13:19958755..19958957 26863196 MeRIP-seq:(Medium) rs1456443382 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3944055,Human_RBP_ID_4276938,Human_RBP_ID_5522263,Human_RBP_ID_8230208,Human_RBP_ID_18417695,Human_RBP_ID_18935960,Human_RBP_ID_18978440 Human_Splice_Rec_1449095,Human_Splice_Rec_1449137,Human_Splice_Rec_1449195 115300 RMVar_ID_115300 Human_SNP_ID_880009015 m1A Human chrX - 154364374 154364374 154364374 CTGGCCCCCTGACAGCTGGGTGGTCTCCCGCTAGGTGAAGGCACGTGGGCCTGGATTGGAGAAGA CTGGCCCCCTGACAGCTGGGTGGTCTCCCGCTCGGTGAAGGCACGTGGGCCTGGATTGGAGAAGA T G FLNA Ensembl:ENSG00000196924 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154364251..154364375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_94455,Human_RBP_ID_5057469,Human_RBP_ID_22693851 RMVar_hsa_circ_120342,RMVar_hsa_circ_111743,RMVar_hsa_circ_105445,RMVar_hsa_circ_104303,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_97011,RMVar_hsa_circ_264289,RMVar_hsa_circ_86329,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_78819,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_122773,RMVar_hsa_circ_264324,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_264342,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_108965,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_87965,RMVar_hsa_circ_88211,RMVar_hsa_circ_87183,RMVar_hsa_circ_264355,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_122930,RMVar_hsa_circ_264348,RMVar_hsa_circ_264366,RMVar_hsa_circ_79058,RMVar_hsa_circ_264370,RMVar_hsa_circ_104073,RMVar_hsa_circ_264373,RMVar_hsa_circ_85690,RMVar_hsa_circ_264375,RMVar_hsa_circ_76219,RMVar_hsa_circ_114776,RMVar_hsa_circ_264374,RMVar_hsa_circ_103794,RMVar_hsa_circ_102272,RMVar_hsa_circ_113166,RMVar_hsa_circ_264384,RMVar_hsa_circ_264385,RMVar_hsa_circ_264387,RMVar_hsa_circ_122785,RMVar_hsa_circ_264390,RMVar_hsa_circ_123777,RMVar_hsa_circ_113667,RMVar_hsa_circ_108020,RMVar_hsa_circ_264394,RMVar_hsa_circ_76841,RMVar_hsa_circ_264395,RMVar_hsa_circ_264392,RMVar_hsa_circ_264393,RMVar_hsa_circ_264391,RMVar_hsa_circ_75605,RMVar_hsa_circ_99074,RMVar_hsa_circ_264407,RMVar_hsa_circ_264409,RMVar_hsa_circ_76357,RMVar_hsa_circ_91786,RMVar_hsa_circ_264410,RMVar_hsa_circ_127623,RMVar_hsa_circ_369673,RMVar_hsa_circ_120029,RMVar_hsa_circ_264416,RMVar_hsa_circ_264417,RMVar_hsa_circ_86800,RMVar_hsa_circ_96481,RMVar_hsa_circ_100372,RMVar_hsa_circ_92546,RMVar_hsa_circ_84283,RMVar_hsa_circ_264420,RMVar_hsa_circ_264424,RMVar_hsa_circ_264422,RMVar_hsa_circ_264423,RMVar_hsa_circ_264421,RMVar_hsa_circ_264418,RMVar_hsa_circ_264419,RMVar_hsa_circ_85464,RMVar_hsa_circ_105311,RMVar_hsa_circ_264437,RMVar_hsa_circ_79822,RMVar_hsa_circ_264436,RMVar_hsa_circ_98810,RMVar_hsa_circ_124754,RMVar_hsa_circ_264439,RMVar_hsa_circ_264440,RMVar_hsa_circ_264441,RMVar_hsa_circ_81763,RMVar_hsa_circ_81782,RMVar_hsa_circ_76577,RMVar_hsa_circ_85088,RMVar_hsa_circ_103284,RMVar_hsa_circ_264444,RMVar_hsa_circ_118986,RMVar_hsa_circ_86332,RMVar_hsa_circ_264447,RMVar_hsa_circ_264449,RMVar_hsa_circ_264448,RMVar_hsa_circ_264446,RMVar_hsa_circ_126822,RMVar_hsa_circ_117384,RMVar_hsa_circ_90561,RMVar_hsa_circ_92234,RMVar_hsa_circ_90225,RMVar_hsa_circ_264452,RMVar_hsa_circ_264454,RMVar_hsa_circ_264455,RMVar_hsa_circ_264453,RMVar_hsa_circ_264450,RMVar_hsa_circ_264451,RMVar_hsa_circ_87816,RMVar_hsa_circ_106423,RMVar_hsa_circ_264461,RMVar_hsa_circ_264462,RMVar_hsa_circ_264464,RMVar_hsa_circ_121384,RMVar_hsa_circ_90435,RMVar_hsa_circ_264466,RMVar_hsa_circ_264467,RMVar_hsa_circ_103668,RMVar_hsa_circ_264468 115301 RMVar_ID_115301 Human_SNP_ID_880014602 m1A Human chrX + 154438828 154438828 154438828 CCCCTGAGTCGATGGGCCGAGGCCGAGACTGGAATGTTGACCTGATTCCCAAATTCCTCATGGCT CCCCTGAGTCGATGGGCCGAGGCCGAGACTGGGATGTTGACCTGATTCCCAAATTCCTCATGGCT A G GDI1 Ensembl:ENSG00000203879 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154438501..154438858 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_848436,Human_RBP_ID_1061671,Human_RBP_ID_2072153,Human_RBP_ID_3977810,Human_RBP_ID_18917396,Human_RBP_ID_19026988,Human_RBP_ID_23217354,Human_RBP_ID_24335145,Human_RBP_ID_27550818 Human_Splice_Rec_2248826,Human_Splice_Rec_2248827,Human_Splice_Rec_2248834,Human_Splice_Rec_2248835,Human_Splice_Rec_2248840,Human_Splice_Rec_2248841,Human_Splice_Rec_2248848,Human_Splice_Rec_2248849,Human_Splice_Rec_2248868,Human_Splice_Rec_2248869,Human_Splice_Rec_2248879,Human_Splice_Rec_2248880,Human_Splice_Rec_2248885,Human_Splice_Rec_2248886,Human_Splice_Rec_2248893,Human_Splice_Rec_2248894,Human_Splice_Rec_2248897,Human_Splice_Rec_2248898 Human_miRNA_ID_2762440,Human_miRNA_ID_2880463 RMVar_hsa_circ_52603 115302 RMVar_ID_115302 Human_SNP_ID_880028976 m1A Human chrX - 153955078 153955078 153955078 AACATGGCCGGGCAGCATGGCTGCTCAAACCCACCCTGCGAGACCCACGAGACGGGCACCACCAA AACATGGCCGGGCAGCATGGCTGCTCAAACCCGCCCTGCGAGACCCACGAGACGGGCACCACCAA T C HCFC1 Ensembl:ENSG00000172534 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153955029..153955185 26863196 MeRIP-seq:(Medium) rs782497232 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_257535,Human_RBP_ID_17328479,Human_RBP_ID_18197650,Human_RBP_ID_22122994,Human_RBP_ID_23099586,Human_RBP_ID_26835167,Human_RBP_ID_27145417,Human_RBP_ID_27380261 RMVar_hsa_circ_106656,RMVar_hsa_circ_123902,RMVar_hsa_circ_121535,RMVar_hsa_circ_113764,RMVar_hsa_circ_264255,RMVar_hsa_circ_90706,RMVar_hsa_circ_75687,RMVar_hsa_circ_264257,RMVar_hsa_circ_264258,RMVar_hsa_circ_264256,RMVar_hsa_circ_264253,RMVar_hsa_circ_264254,RMVar_hsa_circ_124363,RMVar_hsa_circ_124900,RMVar_hsa_circ_91802,RMVar_hsa_circ_120162,RMVar_hsa_circ_264262,RMVar_hsa_circ_264263,RMVar_hsa_circ_264264,RMVar_hsa_circ_89254,RMVar_hsa_circ_264266,RMVar_hsa_circ_264267 115303 RMVar_ID_115303 Human_SNP_ID_880052015 m1A Human chrX + 24055616 24055616 24055616 GTGCAGTGTTTTAAAATATATTTCATTGCAGGATGTTACCAAGTTGACGCCACTTTCACACGAAG GTGCAGTGTTTTAAAATATATTTCATTGCAGGGTGTTACCAAGTTGACGCCACTTTCACACGAAG A G EIF2S3 Ensembl:ENSG00000130741 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:24055601..24055675 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_3977122 Human_Splice_Rec_2192843,Human_Splice_Rec_2192844,Human_Splice_Rec_2192847,Human_Splice_Rec_2192848,Human_Splice_Rec_2192869,Human_Splice_Rec_2192870 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_122556,RMVar_hsa_circ_126313,RMVar_hsa_circ_261789,RMVar_hsa_circ_261790,RMVar_hsa_circ_115201,RMVar_hsa_circ_261791,RMVar_hsa_circ_261793,RMVar_hsa_circ_66392,RMVar_hsa_circ_261792 115304 RMVar_ID_115304 Human_SNP_ID_880059726 m1A Human chrX - 47223674 47223674 47223674 CGTGTGGGGGCCTCTCCAGGGTCACTGCCGCCACCACCACCACTCTCATCCAGGCCTATCTGCTC CGTGTGGGGGCCTCTCCAGGGTCACTGCCGCCGCCACCACCACTCTCATCCAGGCCTATCTGCTC T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:47223651..47223675 26863196 MeRIP-seq:(Medium) rs777199690 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115305 RMVar_ID_115305 Human_SNP_ID_880079331 m1A Human chrX - 153862061 153862061 153862061 TGGCAGCACCGCCTCTTCCCGCCGCCCAGCCCACCCCATGGCCGGCTTTCAGGAGCTCCATACAC TGGCAGCACCGCCTCTTCCCGCCGCCCAGCCCCCCCCATGGCCGGCTTTCAGGAGCTCCATACAC T G L1CAM Ensembl:ENSG00000198910 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:153861807..153862227 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_27550422 Human_miRNA_ID_1706437 115306 RMVar_ID_115306 Human_SNP_ID_880090944 m1A Human chrX - 12976206 12976206 12976206 GAGCAAGCCAAGAGCGAGCGTGAGGAAGAGCCACCCGCCCCGCTGTCTCTGGGCTGGGAACTGCA GAGCAAGCCAAGAGCGAGCGTGAGGAAGAGCCTCCCGCCCCGCTGTCTCTGGGCTGGGAACTGCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:12976201..12976300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115307 RMVar_ID_115307 Human_SNP_ID_880134068 m1A Human chrX - 48901935 48901935 48901935 CAAGGTCTGTGTCTGCATTCCAGTAGTAAGGGAGCCCGCTGTGGGGCCGCAGGAAAGAAGTGTCA CAAGGTCTGTGTCTGCATTCCAGTAGTAAGGGCGCCCGCTGTGGGGCCGCAGGAAAGAAGTGTCA T G RF00017-4575,RF00017-4520 RNACentral:URS0000918622,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chrX:48901926..48902050;chrX:48901926..48901975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - 115308 RMVar_ID_115308 Human_SNP_ID_880166023 m1A Human chrX + 147943304 147943304 147943304 AGTAGACCTTACAGAAATAGGGGGCACGGCAGACGCGGTCCTGGATATACTTCAGGTACAAACTA AGTAGACCTTACAGAAATAGGGGGCACGGCAGGCGCGGTCCTGGATATACTTCAGGTACAAACTA A G FMR1 Ensembl:ENSG00000102081 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:147943245..147943364 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_257909,Human_RBP_ID_800439,Human_RBP_ID_7983748,Human_RBP_ID_8933366,Human_RBP_ID_18146916,Human_RBP_ID_19148624 Human_Splice_Rec_2240715,Human_Splice_Rec_2240743,Human_Splice_Rec_2240772,Human_Splice_Rec_2240831,Human_Splice_Rec_2240883,Human_Splice_Rec_2240949,Human_Splice_Rec_2241022,Human_Splice_Rec_2241043,Human_Splice_Rec_2241077 RMVar_hsa_circ_3707,RMVar_hsa_circ_18335,RMVar_hsa_circ_49289,RMVar_hsa_circ_289781,RMVar_hsa_circ_332529,RMVar_hsa_circ_73538,RMVar_hsa_circ_75448,RMVar_hsa_circ_364681,RMVar_hsa_circ_350522,RMVar_hsa_circ_305484 115309 RMVar_ID_115309 Human_SNP_ID_880190392 m1A Human chrX + 71297887 71297887 71297887 CGCCGTGAAGAAGAGATGCGGCGGCAGCAAGAAGAAATGATGCGGCGACAGCAGGAAGGATTCAA CGCCGTGAAGAAGAGATGCGGCGGCAGCAAGACGAAATGATGCGGCGACAGCAGGAAGGATTCAA A C NONO Ensembl:ENSG00000147140 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71297826..71297968 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_94075,Human_RBP_ID_257447,Human_RBP_ID_848622,Human_RBP_ID_968245,Human_RBP_ID_1717004,Human_RBP_ID_2076850,Human_RBP_ID_3261903,Human_RBP_ID_5071025,Human_RBP_ID_8015496,Human_RBP_ID_8277042,Human_RBP_ID_9409352,Human_RBP_ID_16920237,Human_RBP_ID_18543138,Human_RBP_ID_22841905,Human_RBP_ID_24549942,Human_RBP_ID_26363055,Human_RBP_ID_26572766,Human_RBP_ID_27150483,Human_RBP_ID_27553066,Human_RBP_ID_27833962 Human_Splice_Rec_2215922,Human_Splice_Rec_2215923,Human_Splice_Rec_2215944,Human_Splice_Rec_2215945,Human_Splice_Rec_2215964,Human_Splice_Rec_2215965,Human_Splice_Rec_2215986,Human_Splice_Rec_2215987,Human_Splice_Rec_2215994,Human_Splice_Rec_2215995,Human_Splice_Rec_2216054,Human_Splice_Rec_2216070,Human_Splice_Rec_2216071,Human_Splice_Rec_2216079 RMVar_hsa_circ_20036,RMVar_hsa_circ_118303,RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914,RMVar_hsa_circ_117808,RMVar_hsa_circ_262915,RMVar_hsa_circ_262917,RMVar_hsa_circ_76230,RMVar_hsa_circ_262918,RMVar_hsa_circ_262919,RMVar_hsa_circ_125016 115310 RMVar_ID_115310 Human_SNP_ID_880190478 m1A Human chrX + 24057738 24057738 24057738 AGTTTCCTACGGACATTCCAGGGACCAAAGGGAACTTCAAATTAGTCAGGTGACCTCTCTTTTGC AGTTTCCTACGGACATTCCAGGGACCAAAGGGCACTTCAAATTAGTCAGGTGACCTCTCTTTTGC A C EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:24057663..24060097 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_93846,Human_RBP_ID_733605,Human_RBP_ID_1062172,Human_RBP_ID_1713902,Human_RBP_ID_2073149,Human_RBP_ID_3976356,Human_RBP_ID_7994020,Human_RBP_ID_8717387,Human_RBP_ID_8934725,Human_RBP_ID_9316536,Human_RBP_ID_16865314,Human_RBP_ID_17326003,Human_RBP_ID_17441200,Human_RBP_ID_17554074,Human_RBP_ID_18404588,Human_RBP_ID_18918629,Human_RBP_ID_24338308,Human_RBP_ID_27792577 Human_Splice_Rec_2192852,Human_Splice_Rec_2192874 Human_miRNA_ID_2193918,Human_miRNA_ID_2208125,Human_miRNA_ID_2959571 RMVar_hsa_circ_79355,RMVar_hsa_circ_83149,RMVar_hsa_circ_122556,RMVar_hsa_circ_261789,RMVar_hsa_circ_261790,RMVar_hsa_circ_115201,RMVar_hsa_circ_98236,RMVar_hsa_circ_261793,RMVar_hsa_circ_66392,RMVar_hsa_circ_261792,RMVar_hsa_circ_272846,RMVar_hsa_circ_342326,RMVar_hsa_circ_127276,RMVar_hsa_circ_80047,RMVar_hsa_circ_261795,RMVar_hsa_circ_261797,RMVar_hsa_circ_89700,RMVar_hsa_circ_261796,RMVar_hsa_circ_261794,RMVar_hsa_circ_261798 115311 RMVar_ID_115311 Human_SNP_ID_880205947 m1A Human chrX - 134473418 134473418 134473418 CCATGAGGAATAAACACCCTTTCCAAATCCTCAGCATAATGATTAGGTATGCAAAATAAATCAAG CCATGAGGAATAAACACCCTTTCCAAATCCTCGGCATAATGATTAGGTATGCAAAATAAATCAAG T C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:134473309..134473475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115312 RMVar_ID_115312 Human_SNP_ID_880213061 m1A Human chrX - 101391048 101391048 101391048 TGGATGTTACTCGGCCCCCACCAGCAAGTCCTACCATGCTTGCGTGAGCGCTATCGGCGCGGAAA TGGATGTTACTCGGCCCCCACCAGCAAGTCCTGCCATGCTTGCGTGAGCGCTATCGGCGCGGAAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101391004..101391131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115313 RMVar_ID_115313 Human_SNP_ID_880222311 m1A Human chrX + 119469867 119469867 119469867 AAGCAGATCTTCCTGGGTGGTGTGGACAAGAGAACCCAGTTTTGGCTCTACTTTGCAGGGAATCT AAGCAGATCTTCCTGGGTGGTGTGGACAAGAGGACCCAGTTTTGGCTCTACTTTGCAGGGAATCT A G SLC25A5 Ensembl:ENSG00000005022 Protein coding exon GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:119469766..119469945 26863196 MeRIP-seq:(Medium) rs73637847 Functional Loss SNV ICGC 33..33 33 COCA 8 - Human_RBP_ID_726400,Human_RBP_ID_1710341,Human_RBP_ID_2069289,Human_RBP_ID_5049700,Human_RBP_ID_7969131,Human_RBP_ID_8711832,Human_RBP_ID_9242516,Human_RBP_ID_16800789,Human_RBP_ID_18197360,Human_RBP_ID_22468943,Human_RBP_ID_22840582,Human_RBP_ID_24555701,Human_RBP_ID_26835676,Human_RBP_ID_27378817,Human_RBP_ID_27549415 RMVar_hsa_circ_523 115314 RMVar_ID_115314 Human_SNP_ID_880232910 m1A Human chrX + 74203056 74203056 74203056 GGTGCTGCTGCTACTGTACTTGGGCTTCGCCGAGGTGTACCTGCAGGACCTGCACCCAGACTAGG GGTGCTGCTGCTACTGTACTTGGGCTTCGCCGGGGTGTACCTGCAGGACCTGCACCCAGACTAGG A G RAB11FIP1P1 Ensembl:ENSG00000228492 Pseudogene exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:74203019..74203114 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - RMVar_hsa_circ_263035 115315 RMVar_ID_115315 Human_SNP_ID_880233052 m1A Human chrX - 53562845 53562845 53562845 TCCTTCCAACCTCAGCCAAGCTTCCACCTTGCAGGCCAACCGAGAAGGTGAGAGTGCCGAGGCCA TCCTTCCAACCTCAGCCAAGCTTCCACCTTGCGGGCCAACCGAGAAGGTGAGAGTGCCGAGGCCA T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:53562826..53562925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_257161,Human_RBP_ID_8936600,Human_RBP_ID_9265309,Human_RBP_ID_9409271,Human_RBP_ID_23103034,Human_RBP_ID_26362936 Human_Splice_Rec_2209143,Human_Splice_Rec_2209144,Human_Splice_Rec_2209305,Human_Splice_Rec_2209306,Human_Splice_Rec_2209469,Human_Splice_Rec_2209470 RMVar_hsa_circ_49196,RMVar_hsa_circ_104556,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_262524,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_262543,RMVar_hsa_circ_17855,RMVar_hsa_circ_31763,RMVar_hsa_circ_95244,RMVar_hsa_circ_262550,RMVar_hsa_circ_292102,RMVar_hsa_circ_44445,RMVar_hsa_circ_262554 115316 RMVar_ID_115316 Human_SNP_ID_880245174 m1A Human chrX - 73845822 73845822 73845822 GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCACCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCGCCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC T C XIST Ensembl:ENSG00000229807 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_738890,Human_RBP_ID_5084974,Human_RBP_ID_8020339,Human_RBP_ID_10470673,Human_RBP_ID_16931896,Human_RBP_ID_21859998,Human_RBP_ID_22349547,Human_RBP_ID_22842860,Human_RBP_ID_23105268,Human_RBP_ID_23204115,Human_RBP_ID_23302003,Human_RBP_ID_26291032,Human_RBP_ID_26575241,Human_RBP_ID_27151163 Human_miRNA_ID_3212600 115317 RMVar_ID_115317 Human_SNP_ID_880245177 m1A Human chrX - 73845822 73845822 73845822 GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCACCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC GTATTAGACAAGGAAGCCTTCCCCCCGCCCCCCCCCCCACTCCCAGTCTTCCTTTCCCTTCCAGC T G XIST Ensembl:ENSG00000229807 lincRNA intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs773896635 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_738890,Human_RBP_ID_5084974,Human_RBP_ID_8020339,Human_RBP_ID_10470673,Human_RBP_ID_16931896,Human_RBP_ID_21859998,Human_RBP_ID_22349547,Human_RBP_ID_22842860,Human_RBP_ID_23105268,Human_RBP_ID_23204115,Human_RBP_ID_23302003,Human_RBP_ID_26291032,Human_RBP_ID_26575241,Human_RBP_ID_27151163 Human_miRNA_ID_3212600 115318 RMVar_ID_115318 Human_SNP_ID_880266956 m1A Human chrX - 103586109 103586109 103586109 CAGGCCCTTCTCATCCAACGTTTTCCTCCCCTACCTCCGCCGCACCCCAGCCGCCATTTCTTTCC CAGGCCCTTCTCATCCAACGTTTTCCTCCCCTCCCTCCGCCGCACCCCAGCCGCCATTTCTTTCC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:103586105..103586254 32194978 MeRIP-seq:(Medium) rs981108030 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115319 RMVar_ID_115319 Human_SNP_ID_880270975 m1A Human chrX + 153872651 153872651 153872651 CACTTGAGGCTGATGTCATCTGTGGGGAAGACAACCAGGCGCCGTGGAGACTGTTCCGTGATGAC CACTTGAGGCTGATGTCATCTGTGGGGAAGACGACCAGGCGCCGTGGAGACTGTTCCGTGATGAC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:153872626..153872650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115320 RMVar_ID_115320 Human_SNP_ID_880300714 m1A Human chrX - 43843766 43843766 43843766 TTTGATCCTGATGTCTTACTGTCTTTTCTCCCAGGTATGGCAGCAGCCAAACTTCTGCATGACTC TTTGATCCTGATGTCTTACTGTCTTTTCTCCCTGGTATGGCAGCAGCCAAACTTCTGCATGACTC T A MAOB Ensembl:ENSG00000069535 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:43843737..43843836 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UVM 1 - Human_RBP_ID_22557243 Human_Splice_Rec_2199992,Human_Splice_Rec_2200022 RMVar_hsa_circ_369245 115321 RMVar_ID_115321 Human_SNP_ID_880307148 m1A Human chrX + 118975433 118975433 118975433 GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAGCAGCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC GCGGGCGCGTGGAGCCCGGCGGGCTGGGCAGCCGCCGCCGCCGCCGCTGCGAGTCAACGTGGTGC A C LONRF3 Ensembl:ENSG00000175556 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:118975389..118975491 26863196 MeRIP-seq:(Medium) rs1037145243 Functional Loss SNV ICGC 33..33 33 STAD 2 - 115322 RMVar_ID_115322 Human_SNP_ID_880325715 m1A Human chrX - 16845927 16845925 16845927 CTTTTTTTGTTCTTGTAACAGTTTATTCATGGAGGACACACTGCTAAGATTTCAGATTTTAGCTG CTTTTTTTGTTCTTGTAACAGTTTATTCATGG__GACACACTGCTAAGATTTCAGATTTTAGCTG CCT C RBBP7 Ensembl:ENSG00000102054 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 33..34 33 ESCA 1 - Human_RBP_ID_732590,Human_RBP_ID_1061837,Human_RBP_ID_1713135,Human_RBP_ID_2072555,Human_RBP_ID_7989896,Human_RBP_ID_8716223,Human_RBP_ID_8934297,Human_RBP_ID_16857753,Human_RBP_ID_17325743,Human_RBP_ID_18917865,Human_RBP_ID_24336551,Human_RBP_ID_27792007 Human_Splice_Rec_2188368,Human_Splice_Rec_2188369,Human_Splice_Rec_2188392,Human_Splice_Rec_2188393,Human_Splice_Rec_2188398,Human_Splice_Rec_2188399,Human_Splice_Rec_2188403,Human_Splice_Rec_2188423,Human_Splice_Rec_2188424,Human_Splice_Rec_2188445,Human_Splice_Rec_2188446 RMVar_hsa_circ_22147,RMVar_hsa_circ_9167,RMVar_hsa_circ_62889,RMVar_hsa_circ_359994 115323 RMVar_ID_115323 Human_SNP_ID_880333038 m1A Human chrX - 101625063 101625063 101625063 GCCATTTTTTCCTTGTTCTGTTTTCTTCCCCTAGTCAGTCTATAAATGCAATAGCAGGCGCCAGC GCCATTTTTTCCTTGTTCTGTTTTCTTCCCCTGGTCAGTCTATAAATGCAATAGCAGGCGCCAGC T C ARMCX3-AS1 RNACentral:URS00008C1358 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:101625017..101625209 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 115324 RMVar_ID_115324 Human_SNP_ID_880345365 m1A Human chrX - 136497602 136497602 136497602 TGACGCTGGAGCTGAGCAGAGAAAGGGAGGTCAACCGCGCTCTGCTCGCGCCCCGCCGCCCCCCG TGACGCTGGAGCTGAGCAGAGAAAGGGAGGTCTACCGCGCTCTGCTCGCGCCCCGCCGCCCCCCG T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chrX:136497447..136497669;chrX:136497458..136497653 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - 115325 RMVar_ID_115325 Human_SNP_ID_880355286 m1A Human chrX - 78125427 78125427 78125427 ATCCCAAACAAGCCAAAAAACAGAAGACCCTCACCTTCCAGGAGCTCCAAACTGGCACCACCCCC ATCCCAAACAAGCCAAAAAACAGAAGACCCTCGCCTTCCAGGAGCTCCAAACTGGCACCACCCCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:78125404..78125549 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115326 RMVar_ID_115326 Human_SNP_ID_880488350 m1A Human chrX + 340701 340701 340701 CCTGGGCCGTCCTCTCGCCCGTCCGTCCCCTCACCCTGGGCCGTCCTCTCGCCCGTCCGTCCCCT CCTGGGCCGTCCTCTCGCCCGTCCGTCCCCTCTCCCTGGGCCGTCCTCTCGCCCGTCCGTCCCCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:340631..340759 26863196 MeRIP-seq:(Medium) rs374933158 Functional Loss SNV ICGC 33..33 33 LAML 1 - 115327 RMVar_ID_115327 Human_SNP_ID_880491369 m1A Human chrX + 21977114 21977114 21977114 AGGAGCCATCGACAGATACTGGCCCACCGCCGACGGGCGCCTGGTTGAATATGACATAGATGAAG AGGAGCCATCGACAGATACTGGCCCACCGCCGGCGGGCGCCTGGTTGAATATGACATAGATGAAG A G SMS Ensembl:ENSG00000102172 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:21977028..21977150;chrX:21977051..21977153;chrX:21977025..21977144;chrX:21977029..21977144 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_733304,Human_RBP_ID_7992782,Human_RBP_ID_9245580,Human_RBP_ID_9409100,Human_RBP_ID_24337931,Human_RBP_ID_26362718,Human_RBP_ID_26834593 Human_Splice_Rec_2192324,Human_Splice_Rec_2192338,Human_Splice_Rec_2192354,Human_Splice_Rec_2192364 RMVar_hsa_circ_104311,RMVar_hsa_circ_261729,RMVar_hsa_circ_371817,RMVar_hsa_circ_324725,RMVar_hsa_circ_261732,RMVar_hsa_circ_17369,RMVar_hsa_circ_119349,RMVar_hsa_circ_261733,RMVar_hsa_circ_331323 115328 RMVar_ID_115328 Human_SNP_ID_880498233 m1A Human chrX + 77899533 77899533 77899533 AATTGGCACCAAAGCAGCAGCTGTATTGCCGCAGTTCTAGCTTCACCTTCACGATGTTTCCCTTG AATTGGCACCAAAGCAGCAGCTGTATTGCCGCCGTTCTAGCTTCACCTTCACGATGTTTCCCTTG A C COX7B Ensembl:ENSG00000131174 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:77899451..77899630;chrX:77899451..77899646 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_739776,Human_RBP_ID_1406742,Human_RBP_ID_1719520,Human_RBP_ID_2079141,Human_RBP_ID_5074369,Human_RBP_ID_8723684,Human_RBP_ID_9339990,Human_RBP_ID_17327788,Human_RBP_ID_17442761,Human_RBP_ID_18428052,Human_RBP_ID_18925342,Human_RBP_ID_22349992,Human_RBP_ID_22426785,Human_RBP_ID_22467697,Human_RBP_ID_22520104,Human_RBP_ID_22843354,Human_RBP_ID_26297758,Human_RBP_ID_26573372,Human_RBP_ID_27152014,Human_RBP_ID_27384671 Human_Splice_Rec_2220914,Human_Splice_Rec_2220920,Human_Splice_Rec_2220922,Human_Splice_Rec_2220926 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 115329 RMVar_ID_115329 Human_SNP_ID_880525887 m1A Human chrX - 3524533 3524527 3524533 TGATGGTGGTGATGGTGGTGATGGTGATGGTGATGGTGGTGGTGATGGTGATGGTGGTGATGGTG TGATGGTGGTGATGGTGGTGATGGTGATGGTG______GTGGTGATGGTGATGGTGGTGATGGTG CCACCAT C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:3524496..3524561 26863196 MeRIP-seq:(Medium) rs773456450 Functional Loss DEL ICGC 33..38 33 PRAD 1 - 115330 RMVar_ID_115330 Human_SNP_ID_880542681 m1A Human chrX + 135032475 135032475 135032475 GCGTCGCTGGAGGAACCCGATTCCCTTTCCCGAGACGTTTGACGGCGATACCGACCGACTCCCGG GCGTCGCTGGAGGAACCCGATTCCCTTTCCCGGGACGTTTGACGGCGATACCGACCGACTCCCGG A G RTL8C Ensembl:ENSG00000134590 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:135032351..135032550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_729039,Human_RBP_ID_5079288,Human_RBP_ID_9243733,Human_RBP_ID_22120882,Human_RBP_ID_22344999,Human_RBP_ID_22840835,Human_RBP_ID_24330508,Human_RBP_ID_27144062 115331 RMVar_ID_115331 Human_SNP_ID_880545934 m1A Human chrX + 154764953 154764950 154764953 TAAGAAGAAAAAGGAGCGGAAGTCATTGCCAGAAGAAGATGTAGCCGTGAGTAGTAATGTGTTTG TAAGAAGAAAAAGGAGCGGAAGTCATTGCC___AGAAGATGTAGCCGTGAGTAGTAATGTGTTTG CAGA C DKC1 Ensembl:ENSG00000130826 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:154764876..154764975 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 BRCA 1 - Human_RBP_ID_967682,Human_RBP_ID_2072197,Human_RBP_ID_7987572,Human_RBP_ID_8715627,Human_RBP_ID_9409598,Human_RBP_ID_16850444,Human_RBP_ID_19027015,Human_RBP_ID_19149885,Human_RBP_ID_22519286,Human_RBP_ID_24335314,Human_RBP_ID_24550078,Human_RBP_ID_26362625,Human_RBP_ID_27834279 Human_Splice_Rec_2249836,Human_Splice_Rec_2249837,Human_Splice_Rec_2249862,Human_Splice_Rec_2249864,Human_Splice_Rec_2249865,Human_Splice_Rec_2249891,Human_Splice_Rec_2249892,Human_Splice_Rec_2249906,Human_Splice_Rec_2249907,Human_Splice_Rec_2249924 Human_miRNA_ID_2243784,Human_miRNA_ID_2244798 RMVar_hsa_circ_298805,RMVar_hsa_circ_308949,RMVar_hsa_circ_264582,RMVar_hsa_circ_264583 115332 RMVar_ID_115332 Human_SNP_ID_880559735 m1A Human chrX + 64192059 64192058 64192059 ATTGGGCCGTGGATACATTTGGGCAGTTTCCCACAGATATTCTAAGTCATCATCTTCTTCCTCCT ATTGGGCCGTGGATACATTTGGGCAGTTTCCC_CAGATATTCTAAGTCATCATCTTCTTCCTCCT CA C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:64192009..64192235 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 COAD 1 - 115333 RMVar_ID_115333 Human_SNP_ID_880620220 m1A Human chrX + 119560367 119560367 119560367 TCACACGGGACCGGTCCCGGGGCCTCATGGGCAATTTCTCTAACTGGCAGTCTGAAGGAATGGAG TCACACGGGACCGGTCCCGGGGCCTCATGGGCGATTTCTCTAACTGGCAGTCTGAAGGAATGGAG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:119560287..119560458 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LAML 2 - 115334 RMVar_ID_115334 Human_SNP_ID_880626501 m1A Human chrX - 74583188 74583188 74583188 TCTTCATATGCTCAAGTCTCCAGAGTCACTCCATTCTAAGGTTGATGAAGCTGTAGCTGTACTAC TCTTCATATGCTCAAGTCTCCAGAGTCACTCCGTTCTAAGGTTGATGAAGCTGTAGCTGTACTAC T C RLIM,PABPC1P3 Ensembl:ENSG00000131263,Ensembl:ENSG00000230673 Protein coding,Pseudogene 3'UTR,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879005635 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115335 RMVar_ID_115335 Human_SNP_ID_880641792 m1A Human chrX - 48823282 48823282 48823282 CCAACAGCATCCTCTGAGGTGGTCTGGTCCAGAATGGCTCCTCCCACAGTCTCCTCTGAGGTGGT CCAACAGCATCCTCTGAGGTGGTCTGGTCCAGCATGGCTCCTCCCACAGTCTCCTCTGAGGTGGT T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48823234..48823476 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - RMVar_hsa_circ_78757,RMVar_hsa_circ_262392 115336 RMVar_ID_115336 Human_SNP_ID_880643153 m1A Human chrX + 151672384 151672384 151672384 GGCGGCAAAAGAAGAAGAAGCTACAGGAGCGGAAGAAGTGGCAGGGGCAGATGCTACAGAAAGAG GGCGGCAAAAGAAGAAGAAGCTACAGGAGCGGTAGAAGTGGCAGGGGCAGATGCTACAGAAAGAG A T PASD1 Ensembl:ENSG00000166049 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:151672254..151672512 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - RMVar_hsa_circ_93154,RMVar_hsa_circ_264146 115337 RMVar_ID_115337 Human_SNP_ID_880650521 m1A Human chrX - 11114953 11114953 11114953 AGATTTGAAGGATCTAGGTTCTCCTTATTCTCAGCCGCAGTGCCCCTAATGGGACACTCCACGTA AGATTTGAAGGATCTAGGTTCTCCTTATTCTCGGCCGCAGTGCCCCTAATGGGACACTCCACGTA T C lnc-ARHGAP6-3 RNACentral:URS00008B5AB0 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:11114902..11115031 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115338 RMVar_ID_115338 Human_SNP_ID_880678795 m1A Human chrX - 19970284 19970284 19970284 TCCTGTGTTTCTTTGCAGTGTAAAAAGTGGATAGTGGCTCACGTGTCAAAGGATGGCACGGTCAC TCCTGTGTTTCTTTGCAGTGTAAAAAGTGGATGGTGGCTCACGTGTCAAAGGATGGCACGGTCAC T C BCLAF3 Ensembl:ENSG00000173681 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:19970237..19970343;chrX:19970235..19970328 26863196 MeRIP-seq:(Medium) rs557627256 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_24337462 Human_Splice_Rec_2190400,Human_Splice_Rec_2190448 RMVar_hsa_circ_291158,RMVar_hsa_circ_261635,RMVar_hsa_circ_271810,RMVar_hsa_circ_261642,RMVar_hsa_circ_274628,RMVar_hsa_circ_261643,RMVar_hsa_circ_271162,RMVar_hsa_circ_261646,RMVar_hsa_circ_328252,RMVar_hsa_circ_261648,RMVar_hsa_circ_291849,RMVar_hsa_circ_261650 115339 RMVar_ID_115339 Human_SNP_ID_880683439 m1A Human chrX - 154439970 154439970 154439970 GAAGTTTGCCACAAACACCAGGAACTTGCGGAAGCGCCGTTTCTCAAACATGCCCATCAGATCTA GAAGTTTGCCACAAACACCAGGAACTTGCGGATGCGCCGTTTCTCAAACATGCCCATCAGATCTA T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154439951..154440000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115340 RMVar_ID_115340 Human_SNP_ID_880706702 m1A Human chrX - 101276429 101276429 101276429 TGATGAAGATGAGGATGAGGATGAGGATGAGGATGAAGATGAAGACAAAGAAGAGGAGGAGGAAG TGATGAAGATGAGGATGAGGATGAGGATGAGGGTGAAGATGAAGACAAAGAAGAGGAGGAGGAAG T C TAF7L Ensembl:ENSG00000102387 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101276389..101276477 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_Splice_Rec_2223717,Human_Splice_Rec_2223761 115341 RMVar_ID_115341 Human_SNP_ID_880796175 m1A Human chrX + 70290546 70290546 70290546 TGGTCCCCAAAGAGATTAGCGAGGGCTGCCAGATGTGCCTTTCCTTCGTGCCCGGAGAGCCTCAG TGGTCCCCAAAGAGATTAGCGAGGGCTGCCAGTTGTGCCTTTCCTTCGTGCCCGGAGAGCCTCAG A T KIF4A Ensembl:ENSG00000090889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:70290495..70290592 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_966716,Human_RBP_ID_9317561,Human_RBP_ID_24349445 Human_Splice_Rec_2214240,Human_Splice_Rec_2214300 Human_miRNA_ID_1965028,Human_miRNA_ID_1971910,Human_miRNA_ID_2764482 RMVar_hsa_circ_17844,RMVar_hsa_circ_92644,RMVar_hsa_circ_365238,RMVar_hsa_circ_73513,RMVar_hsa_circ_262849 115342 RMVar_ID_115342 Human_SNP_ID_880833648 m1A Human chrX - 49165385 49165385 49165385 GTGAACCTCTCCCTTCTCCTCACTGATCTCTGACTTCTCTCCCTTGGGAAACCCACCAACTCCTT GTGAACCTCTCCCTTCTCCTCACTGATCTCTGGCTTCTCTCCCTTGGGAAACCCACCAACTCCTT T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:49165369..49165434 26863196 MeRIP-seq:(Medium) rs147071787 Functional Loss SNV ICGC 33..33 33 LAML 1 - 115343 RMVar_ID_115343 Human_SNP_ID_880838189 m1A Human chrX - 1391900 1391900 1391900 GGCTCCGATCGAGCGGGTCAAGCTGCTGCTGCAGGTGGGGACGCGGGCGCGGCCGCTCCGGGGAC GGCTCCGATCGAGCGGGTCAAGCTGCTGCTGCGGGTGGGGACGCGGGCGCGGCCGCTCCGGGGAC T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1341466,Human_RBP_ID_19148842,Human_RBP_ID_26797219 Human_Splice_Rec_2182669 RMVar_hsa_circ_120927,RMVar_hsa_circ_261183 115344 RMVar_ID_115344 Human_SNP_ID_880851880 m1A Human chrX - 53082401 53082401 53082401 CGCTAGTCGCACCGGTAAGCAGAGCTGAGGAGACTCACGCAACCAGCTCTCCTCACCACCTCGCT CGCTAGTCGCACCGGTAAGCAGAGCTGAGGAGCCTCACGCAACCAGCTCTCCTCACCACCTCGCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:53082351..53083266 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115345 RMVar_ID_115345 Human_SNP_ID_880884299 m1A Human chrX + 13745 13745 13745 GGGACCACCCCCAGACCCCCGCTCCTCCCCTCAGGACCACCCCCAGATCCACTGTTCCTGTCCTC GGGACCACCCCCAGACCCCCGCTCCTCCCCTCGGGACCACCCCCAGATCCACTGTTCCTGTCCTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:13700..13772 26863196 MeRIP-seq:(Medium) rs368125700 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115346 RMVar_ID_115346 Human_SNP_ID_880887004 m1A Human chrX - 154352367 154352367 154352367 AGACCCATGAGGCCGAGATCGTGGAAGGGGAGAACCACACCTACTGCATCCGCTTTGTTCCCGCT AGACCCATGAGGCCGAGATCGTGGAAGGGGAGGACCACACCTACTGCATCCGCTTTGTTCCCGCT T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154352183..154352373 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_799897,Human_RBP_ID_2072097,Human_RBP_ID_3918992,Human_RBP_ID_5057234,Human_RBP_ID_5640689,Human_RBP_ID_8933948,Human_RBP_ID_9265439,Human_RBP_ID_9318151,Human_RBP_ID_17717911,Human_RBP_ID_18197449,Human_RBP_ID_23317686 Human_Splice_Rec_2247402,Human_Splice_Rec_2247492,Human_Splice_Rec_2247582,Human_Splice_Rec_2247675,Human_Splice_Rec_2247766,Human_Splice_Rec_2247896,Human_Splice_Rec_2247924,Human_Splice_Rec_2247932 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_1608,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_97350,RMVar_hsa_circ_264326,RMVar_hsa_circ_35178,RMVar_hsa_circ_46907,RMVar_hsa_circ_264328,RMVar_hsa_circ_264329,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_108906,RMVar_hsa_circ_78188,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264331,RMVar_hsa_circ_264332,RMVar_hsa_circ_264333,RMVar_hsa_circ_125720,RMVar_hsa_circ_264792,RMVar_hsa_circ_114261,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264340,RMVar_hsa_circ_264341,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335 115347 RMVar_ID_115347 Human_SNP_ID_880888983 m1A Human chrX + 16853733 16853733 16853733 CAGCAACAGATCCAAACAATGACTCGTGCAGCAGGTGCCAGGCCACATCCTCTACAACAGCTGAG CAGCAACAGATCCAAACAATGACTCGTGCAGCGGGTGCCAGGCCACATCCTCTACAACAGCTGAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:16853652..16853742 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115348 RMVar_ID_115348 Human_SNP_ID_880951491 m1A Human chrX + 48575239 48575239 48575239 CGTGGGAGGGCTCAACTTTAACACCGACGAGCAGGCACTGGAAGACCACTTCAGCAGTTTCGGAC CGTGGGAGGGCTCAACTTTAACACCGACGAGCTGGCACTGGAAGACCACTTCAGCAGTTTCGGAC A T RBM3 Ensembl:ENSG00000102317 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:48575189..48575309 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_93591,Human_RBP_ID_735541,Human_RBP_ID_799380,Human_RBP_ID_848909,Human_RBP_ID_1062658,Human_RBP_ID_1715597,Human_RBP_ID_2075221,Human_RBP_ID_3923712,Human_RBP_ID_5065370,Human_RBP_ID_8006551,Human_RBP_ID_8719673,Human_RBP_ID_16898864,Human_RBP_ID_17326420,Human_RBP_ID_22467578,Human_RBP_ID_23120992,Human_RBP_ID_24343873,Human_RBP_ID_26834745 Human_Splice_Rec_2203300,Human_Splice_Rec_2203301,Human_Splice_Rec_2203307,Human_Splice_Rec_2203308,Human_Splice_Rec_2203313,Human_Splice_Rec_2203314,Human_Splice_Rec_2203325,Human_Splice_Rec_2203326,Human_Splice_Rec_2203339,Human_Splice_Rec_2203340,Human_Splice_Rec_2203349,Human_Splice_Rec_2203351,Human_Splice_Rec_2203352,Human_Splice_Rec_2203361,Human_Splice_Rec_2203362,Human_Splice_Rec_2203364,Human_Splice_Rec_2203374 RMVar_hsa_circ_60709,RMVar_hsa_circ_262366,RMVar_hsa_circ_76894,RMVar_hsa_circ_113506,RMVar_hsa_circ_262367,RMVar_hsa_circ_301042,RMVar_hsa_circ_374765,RMVar_hsa_circ_375083,RMVar_hsa_circ_85851,RMVar_hsa_circ_262368,RMVar_hsa_circ_262370,RMVar_hsa_circ_262371,RMVar_hsa_circ_262369 115349 RMVar_ID_115349 Human_SNP_ID_880994324 m1A Human chrX - 48597998 48597998 48597998 CCACTGCTAAGACTTGCTGCCACACCGCGGCCATTCCCCGGCCTCCTCCTCTGGCGTGTCCGCCC CCACTGCTAAGACTTGCTGCCACACCGCGGCCTTTCCCCGGCCTCCTCCTCTGGCGTGTCCGCCC T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:48597851..48598050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115350 RMVar_ID_115350 Human_SNP_ID_881016672 m1A Human chrX - 53394872 53394872 53394872 TCCGTTGCCATTGCAGGGTAGCTCCCAGGGGGAGGACTCAGTGAGTGGTTCACAGAGAATTTCCA TCCGTTGCCATTGCAGGGTAGCTCCCAGGGGGGGGACTCAGTGAGTGGTTCACAGAGAATTTCCA T C SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53394826..53394900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_16390,Human_RBP_ID_92922,Human_RBP_ID_257110,Human_RBP_ID_736456,Human_RBP_ID_967794,Human_RBP_ID_1716111,Human_RBP_ID_2075645,Human_RBP_ID_8008927,Human_RBP_ID_8936285,Human_RBP_ID_9317427,Human_RBP_ID_16904374,Human_RBP_ID_18152227,Human_RBP_ID_18414661,Human_RBP_ID_18545127,Human_RBP_ID_18921395,Human_RBP_ID_24346489,Human_RBP_ID_26362870,Human_RBP_ID_27794079 Human_Splice_Rec_2208841,Human_Splice_Rec_2208842,Human_Splice_Rec_2208890,Human_Splice_Rec_2208891,Human_Splice_Rec_2208904,Human_Splice_Rec_2208905 RMVar_hsa_circ_9378,RMVar_hsa_circ_59814,RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_304627,RMVar_hsa_circ_50880,RMVar_hsa_circ_262491 115351 RMVar_ID_115351 Human_SNP_ID_881022375 m1A Human chrX - 149935041 149935040 149935041 GTAGGGGCAGCTCAAGGGTGGAGTTCAGGGCCAGGGGGCGGGGCCACGGGCCTGAGGGGTGAGGG GTAGGGGCAGCTCAAGGGTGGAGTTCAGGGCC_GGGGGCGGGGCCACGGGCCTGAGGGGTGAGGG CT C EOLA2 Ensembl:ENSG00000197021 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:149934947..149935093 26863196 MeRIP-seq:(Medium) rs782025249 Functional Loss DEL ICGC 33..33 33 PBCA 1 - Human_RBP_ID_3930386,Human_RBP_ID_9443545 115352 RMVar_ID_115352 Human_SNP_ID_881118301 m1A Human chrX - 65518199 65518199 65518199 TAATGATGTCAAGGAAGAGGAGAAGGAGGAGAAAGAGGTCTTGCCAGACCAGGTAGAGGAGGAGG TAATGATGTCAAGGAAGAGGAGAAGGAGGAGACAGAGGTCTTGCCAGACCAGGTAGAGGAGGAGG T G LAS1L Ensembl:ENSG00000001497 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:65518014..65518275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_1719925,Human_RBP_ID_5069573,Human_RBP_ID_8013404,Human_RBP_ID_22122827,Human_RBP_ID_23107495,Human_RBP_ID_24549929,Human_RBP_ID_26362981 RMVar_hsa_circ_91590,RMVar_hsa_circ_104698,RMVar_hsa_circ_121718,RMVar_hsa_circ_99995,RMVar_hsa_circ_66050,RMVar_hsa_circ_262745,RMVar_hsa_circ_262747,RMVar_hsa_circ_262748,RMVar_hsa_circ_262746,RMVar_hsa_circ_68469 115353 RMVar_ID_115353 Human_SNP_ID_881151964 m1A Human chrX - 71366427 71366427 71366427 CTCCATTGATGTTGCCGAAAAGGAAACCCGCTAAAGAAAATGGGCCGCCTCCAGCGGAATCTTCG CTCCATTGATGTTGCCGAAAAGGAAACCCGCTGAAGAAAATGGGCCGCCTCCAGCGGAATCTTCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71366380..71366720 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115354 RMVar_ID_115354 Human_SNP_ID_881164045 m1A Human chrX - 153869637 153869637 153869637 GCACAGAGCTGGCCAAAGACCAGAAGTACCGGATTCAGCGTGGCGCCCTGATCCTGAGCAACGTG GCACAGAGCTGGCCAAAGACCAGAAGTACCGGGTTCAGCGTGGCGCCCTGATCCTGAGCAACGTG T C L1CAM Ensembl:ENSG00000198910 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:153869590..153869671 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - Human_RBP_ID_94529 Human_Splice_Rec_2245698,Human_Splice_Rec_2245752,Human_Splice_Rec_2245806,Human_Splice_Rec_2245862 RMVar_hsa_circ_103305,RMVar_hsa_circ_264232,RMVar_hsa_circ_371973,RMVar_hsa_circ_107906,RMVar_hsa_circ_467,RMVar_hsa_circ_264234,RMVar_hsa_circ_264235,RMVar_hsa_circ_50098,RMVar_hsa_circ_264238,RMVar_hsa_circ_268273,RMVar_hsa_circ_370460 115355 RMVar_ID_115355 Human_SNP_ID_881178348 m1A Human chrX - 123732982 123732982 123732982 CGCGGCTGTGGTGGTTCCCGCAGAGTGGATAAAGAACTGGGAGAAATCAGGGAGAGGCGAATTGT CGCGGCTGTGGTGGTTCCCGCAGAGTGGATAACGAACTGGGAGAAATCAGGGAGAGGCGAATTGT T G THOC2 Ensembl:ENSG00000125676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:123732946..123733033 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_1060888,Human_RBP_ID_3977648,Human_RBP_ID_8938843,Human_RBP_ID_9317595,Human_RBP_ID_9410115,Human_RBP_ID_16810822,Human_RBP_ID_18427884,Human_RBP_ID_18914927,Human_RBP_ID_19027641,Human_RBP_ID_26363332,Human_RBP_ID_26772785,Human_RBP_ID_27834131 Human_Splice_Rec_2233276,Human_Splice_Rec_2233406,Human_Splice_Rec_2233580 115356 RMVar_ID_115356 Human_SNP_ID_881192089 m1A Human chrX - 12975645 12975645 12975645 GCCCCGAAGCCGGTCTTGCCTGCTCTCCCGGCAATTCGGCATCCCTGGCACACATGTCTCTGCAA GCCCCGAAGCCGGTCTTGCCTGCTCTCCCGGCTATTCGGCATCCCTGGCACACATGTCTCTGCAA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:12975643..12975741 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 115357 RMVar_ID_115357 Human_SNP_ID_881239989 m1A Human chrX + 53432025 53432025 53432025 CCTCGAAGGCAGCCACACTGGCAGTGTTGATGATGACCCCACGTTGGCCTCCCTGGTCTGGTTCA CCTCGAAGGCAGCCACACTGGCAGTGTTGATGGTGACCCCACGTTGGCCTCCCTGGTCTGGTTCA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53431774..53432136 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 115358 RMVar_ID_115358 Human_SNP_ID_881240826 m1A Human chrX + 153954203 153954203 153954203 GAGCCAGCAGCGCGGTGCCAGCCTGGGGGGTGACGCTGGGTGCCGCCGCCACCTCTAGGCCAGAC GAGCCAGCAGCGCGGTGCCAGCCTGGGGGGTGGCGCTGGGTGCCGCCGCCACCTCTAGGCCAGAC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153954152..153954329 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 115359 RMVar_ID_115359 Human_SNP_ID_881266589 m1A Human chrX - 13379047 13379047 13379047 GAAGAGATTCTGAATTCCCTCAAGTACGTCCGACCTGGTGGTGGGTTCGAGCCCAACTTCATGCT GAAGAGATTCTGAATTCCCTCAAGTACGTCCGGCCTGGTGGTGGGTTCGAGCCCAACTTCATGCT T C GPX1P1 Ensembl:ENSG00000197582 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879163336 Functional Loss SNV ICGC 33..33 33 STAD 1 - 115360 RMVar_ID_115360 Human_SNP_ID_881269451 m1A Human chrX - 108732954 108732954 108732954 TCGCTTCGGCTGCAGAGCCGACTTTAGCCCTCAGCCAAGTTGTAGCTGCGGCCTCCGCGCTCGCC TCGCTTCGGCTGCAGAGCCGACTTTAGCCCTCGGCCAAGTTGTAGCTGCGGCCTCCGCGCTCGCC T C IRS4 Ensembl:ENSG00000133124 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:108732852..108733000 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_8932008,Human_RBP_ID_16789135,Human_RBP_ID_17324475,Human_RBP_ID_17552113,Human_RBP_ID_23108024,Human_RBP_ID_26302248 115361 RMVar_ID_115361 Human_SNP_ID_881305554 m1A Human chrX - 119469757 119469757 119469757 TCTGATGACATTGGCCAGGTTACCGCGCCAGAAGGACAGAACTCCCTGCTCCTTGGGAATACGGA TCTGATGACATTGGCCAGGTTACCGCGCCAGACGGACAGAACTCCCTGCTCCTTGGGAATACGGA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:119469625..119470182 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 KIRP 2 - 115362 RMVar_ID_115362 Human_SNP_ID_881322035 m1A Human chrX - 53591102 53591102 53591102 TTCTTTATGTAGCTCATGGACATGGGCTTCACAAGGGAACATGCAATGGAGGCACTGTTGAACAC TTCTTTATGTAGCTCATGGACATGGGCTTCACCAGGGAACATGCAATGGAGGCACTGTTGAACAC T G HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:53591101..53591125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_93181,Human_RBP_ID_966352,Human_RBP_ID_1342557,Human_RBP_ID_1405864,Human_RBP_ID_3924574,Human_RBP_ID_5068148,Human_RBP_ID_5535672,Human_RBP_ID_8936719,Human_RBP_ID_9352119,Human_RBP_ID_17326703,Human_RBP_ID_17554944,Human_RBP_ID_18921723,Human_RBP_ID_22693317 Human_Splice_Rec_2209106,Human_Splice_Rec_2209267,Human_Splice_Rec_2209431,Human_Splice_Rec_2209624 Human_miRNA_ID_267249,Human_miRNA_ID_2048639,Human_miRNA_ID_2473779,Human_miRNA_ID_2959574 RMVar_hsa_circ_490,RMVar_hsa_circ_49196,RMVar_hsa_circ_17855,RMVar_hsa_circ_101893,RMVar_hsa_circ_262559,RMVar_hsa_circ_104969,RMVar_hsa_circ_262560,RMVar_hsa_circ_370348,RMVar_hsa_circ_40553,RMVar_hsa_circ_49868,RMVar_hsa_circ_7144,RMVar_hsa_circ_31413,RMVar_hsa_circ_262562,RMVar_hsa_circ_375687,RMVar_hsa_circ_318971,RMVar_hsa_circ_262565,RMVar_hsa_circ_352912,RMVar_hsa_circ_17816,RMVar_hsa_circ_11755,RMVar_hsa_circ_262566,RMVar_hsa_circ_370607,RMVar_hsa_circ_262567 115363 RMVar_ID_115363 Human_SNP_ID_881323092 m1A Human chrX - 1389212 1389212 1389212 AAGGGTACGTGTGGCTGCCATCGCGAAGTCCCAGAGACGGGCTCAACACACAGACGTTCCCCCAG AAGGGTACGTGTGGCTGCCATCGCGAAGTCCCGGAGACGGGCTCAACACACAGACGTTCCCCCAG T C SLC25A6 Ensembl:ENSG00000169100 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:1389209..1389760 26863196 MeRIP-seq:(Medium) rs769077785 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_19148157 Human_miRNA_ID_2425966,Human_miRNA_ID_2425967,Human_miRNA_ID_2435637,Human_miRNA_ID_2435638 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183 115364 RMVar_ID_115364 Human_SNP_ID_881332799 m1A Human chrX - 107714686 107714686 107714686 TGAGAGAGGAGGTGGAGATCCTGAAGGAGCAGATCCGAGAGCTGGTGGAGAAGAACTCCCAGCTA TGAGAGAGGAGGTGGAGATCCTGAAGGAGCAGCTCCGAGAGCTGGTGGAGAAGAACTCCCAGCTA T G TSC22D3 Ensembl:ENSG00000157514 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:107714635..107714708 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_258091,Human_RBP_ID_725112,Human_RBP_ID_1709781,Human_RBP_ID_2068507,Human_RBP_ID_5047242,Human_RBP_ID_7964296,Human_RBP_ID_8710751,Human_RBP_ID_8931847,Human_RBP_ID_16786889,Human_RBP_ID_24321663 Human_Splice_Rec_2227471,Human_Splice_Rec_2227475,Human_Splice_Rec_2227481,Human_Splice_Rec_2227485,Human_Splice_Rec_2227491,Human_Splice_Rec_2227495,Human_Splice_Rec_2227501,Human_Splice_Rec_2227507,Human_Splice_Rec_2227509 115365 RMVar_ID_115365 Human_SNP_ID_881338359 m1A Human chrX + 53279658 53279658 53279658 GCAATACTGGTGTAGAGTATGAGACGCTGTGGACCTGAGAGACAGCAAGAGACAGAGAGAGACAG GCAATACTGGTGTAGAGTATGAGACGCTGTGGGCCTGAGAGACAGCAAGAGACAGAGAGAGACAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:53279609..53279798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115366 RMVar_ID_115366 Human_SNP_ID_881362561 m1A Human chrX - 78109882 78109882 78109882 TGGTTGTTTGTTATCTGGTTGTTCTTCATAGGAACATTGAAGTCGACTCTAAAAAAGAAAGATGC TGGTTGTTTGTTATCTGGTTGTTCTTCATAGGTACATTGAAGTCGACTCTAAAAAAGAAAGATGC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:78109851..78109925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115367 RMVar_ID_115367 Human_SNP_ID_881366798 m1A Human chrX + 47566665 47566665 47566665 TGGCAGCCCCCGCACCCAGCACTGTGACCCGGAGCACTTCCCCTTCCCTGCCCCAGCCAATGCCC TGGCAGCCCCCGCACCCAGCACTGTGACCCGGGGCACTTCCCCTTCCCTGCCCCAGCCAATGCCC A G ARAF Ensembl:ENSG00000078061 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chrX:47566651..47566775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_799168,Human_RBP_ID_8719528,Human_RBP_ID_18920597,Human_RBP_ID_18963927 Human_Splice_Rec_2201846,Human_Splice_Rec_2201875 Human_miRNA_ID_2317170,Human_miRNA_ID_2320324,Human_miRNA_ID_2323478,Human_miRNA_ID_2326654,Human_miRNA_ID_2329741,Human_miRNA_ID_2386132,Human_miRNA_ID_2521031,Human_miRNA_ID_2524199,Human_miRNA_ID_2823380,Human_miRNA_ID_2829511,Human_miRNA_ID_2832668,Human_miRNA_ID_2836795,Human_miRNA_ID_2842143 RMVar_hsa_circ_126962,RMVar_hsa_circ_262322 115368 RMVar_ID_115368 Human_SNP_ID_881368033 m1A Human chrX + 40664373 40664373 40664373 AACCGGAGAATGTAGTGAGGGGTTGGCTGGTGACATTCCAGGCATGCGTGCTGCTGGTGAGGGGC AACCGGAGAATGTAGTGAGGGGTTGGCTGGTGTCATTCCAGGCATGCGTGCTGCTGGTGAGGGGC A T RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:40664262..40664391 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 115369 RMVar_ID_115369 Human_SNP_ID_881379758 m1A Human chrX - 53547891 53547891 53547891 TGCTCTCCCAGAAAACAAGGTGTCAGAAGCACAGGCTAATTCTGGCAGCGGTGCTTCCTCCACCA TGCTCTCCCAGAAAACAAGGTGTCAGAAGCACGGGCTAATTCTGGCAGCGGTGCTTCCTCCACCA T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:53547713..53547899 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_2075828,Human_RBP_ID_9339965,Human_RBP_ID_17328065,Human_RBP_ID_17441798,Human_RBP_ID_17554892,Human_RBP_ID_21837747,Human_RBP_ID_22468366,Human_RBP_ID_24555760,Human_RBP_ID_27382984 Human_miRNA_ID_2237974 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 115370 RMVar_ID_115370 Human_SNP_ID_881413107 m1A Human chrX + 72274067 72274063 72274067 AGGAACCATGGGTTCCCTAACTGCTGCAGATTAATTGTGACGCTGATCGTTCTTTCCACCCTCAA AGGAACCATGGGTTCCCTAACTGCTGCAG____ATTGTGACGCTGATCGTTCTTTCCACCCTCAA GATTA G PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:72274065..72274233 26863196 MeRIP-seq:(Medium) rs756971490 Functional Loss DEL TCGA 30..33 33 TGCT 1 - 115371 RMVar_ID_115371 Human_SNP_ID_881413720 m1A Human chrX - 153788133 153788133 153788133 GTGCCACTAAGCCTGTGTTGTGTTTTGTAGGCAACATCGAAACCAACCATAACCTGCCACCGTCG GTGCCACTAAGCCTGTGTTGTGTTTTGTAGGCTACATCGAAACCAACCATAACCTGCCACCGTCG T A IDH3G Ensembl:ENSG00000067829 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153787592..153788134 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_5124802 Human_Splice_Rec_2245309,Human_Splice_Rec_2245310,Human_Splice_Rec_2245339,Human_Splice_Rec_2245340,Human_Splice_Rec_2245359,Human_Splice_Rec_2245360,Human_Splice_Rec_2245381,Human_Splice_Rec_2245382,Human_Splice_Rec_2245400,Human_Splice_Rec_2245401,Human_Splice_Rec_2245422,Human_Splice_Rec_2245423,Human_Splice_Rec_2245433,Human_Splice_Rec_2245448,Human_Splice_Rec_2245449,Human_Splice_Rec_2245464,Human_Splice_Rec_2245465,Human_Splice_Rec_2245478,Human_Splice_Rec_2245479 Human_miRNA_ID_2924209 RMVar_hsa_circ_94526,RMVar_hsa_circ_264224 115372 RMVar_ID_115372 Human_SNP_ID_881457936 m1A Human chrX + 154354667 154354667 154354667 TGGGCGTAGGTGTACTGTGGGGCCAGCTGCTGAGACCGTAGAGGGGGCTGCACCGAGGGCTGGTC TGGGCGTAGGTGTACTGTGGGGCCAGCTGCTGCGACCGTAGAGGGGGCTGCACCGAGGGCTGGTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154354616..154354731 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 115373 RMVar_ID_115373 Human_SNP_ID_881491257 m1A Human chrX - 79363553 79363553 79363553 TTTGTTTTTGGTTTTGCTTTTTAATAAATAGGAGCTCCGAGTTGCCACCCAGGAAAAAGAGGGCT TTTGTTTTTGGTTTTGCTTTTTAATAAATAGGGGCTCCGAGTTGCCACCCAGGAAAAAGAGGGCT T C ITM2A Ensembl:ENSG00000078596 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:79362959..79363575 32194978 MeRIP-seq:(Medium) rs1360197652 Functional Loss SNV TCGA,ICGC 33..33 33 PRAD 2 - Human_Splice_Rec_2221221,Human_Splice_Rec_2221239 115374 RMVar_ID_115374 Human_SNP_ID_881498162 m1A Human chrX - 1386696 1386696 1386696 TTGGAGGAAGATCTTCAGAGATGAGGGGGGCAAGGCCTTCTTCAAGGGTGCGTGGTCCAACGTCC TTGGAGGAAGATCTTCAGAGATGAGGGGGGCAGGGCCTTCTTCAAGGGTGCGTGGTCCAACGTCC T C SLC25A6 Ensembl:ENSG00000169100 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chrX:1386676..1386700;chrX:1386387..1386775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_1712166,Human_RBP_ID_18147403,Human_RBP_ID_18197249 Human_miRNA_ID_1966882,Human_miRNA_ID_1966883,Human_miRNA_ID_1966884,Human_miRNA_ID_1966885,Human_miRNA_ID_2362338,Human_miRNA_ID_2362339,Human_miRNA_ID_2362340,Human_miRNA_ID_2362341 RMVar_hsa_circ_78573,RMVar_hsa_circ_120927,RMVar_hsa_circ_127294,RMVar_hsa_circ_89907,RMVar_hsa_circ_261180,RMVar_hsa_circ_261182,RMVar_hsa_circ_261183,RMVar_hsa_circ_261181 115375 RMVar_ID_115375 Human_SNP_ID_881511569 m1A Human chrX + 154450258 154450258 154450258 GGTGCTGAGGAGCTGGTACGAGAAGAACAAGCACATCTTTCCCGCCAGCCGCTGGGAACCCTACG GGTGCTGAGGAGCTGGTACGAGAAGAACAAGCGCATCTTTCCCGCCAGCCGCTGGGAACCCTACG A G FAM50A Ensembl:ENSG00000071859 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:154450104..154450650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - Human_RBP_ID_92903,Human_RBP_ID_257099,Human_RBP_ID_5058069,Human_RBP_ID_19026997,Human_RBP_ID_23099768,Human_RBP_ID_27146148 Human_Splice_Rec_2248945,Human_Splice_Rec_2248946,Human_Splice_Rec_2248967,Human_Splice_Rec_2248968,Human_Splice_Rec_2249011 Human_miRNA_ID_2238003 RMVar_hsa_circ_83086,RMVar_hsa_circ_264522,RMVar_hsa_circ_90392,RMVar_hsa_circ_264528,RMVar_hsa_circ_100197,RMVar_hsa_circ_81099,RMVar_hsa_circ_264530,RMVar_hsa_circ_264531 115376 RMVar_ID_115376 Human_SNP_ID_881514764 m1A Human chrX + 103377475 103377474 103377475 TGTCTTACTTGTGTTCAAAGAAAAACAACCAGAAAAAAAAAATCTCATCATGGCAAATATTCACC TGTCTTACTTGTGTTCAAAGAAAAACAACCAG_AAAAAAAAATCTCATCATGGCAAATATTCACC GA G BEX3 Ensembl:ENSG00000166681 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-IP-seq;HEK-293T cells,m1A-quant-seq - 31548705 m1A-IP-seq&m1A-quant-seq:(High) rs199898496 Functional Loss DEL TCGA,ICGC 33..33 33 COCA,UCEC 3 - Human_RBP_ID_8710347,Human_RBP_ID_27140969 Human_Splice_Rec_2225835,Human_Splice_Rec_2225837 RMVar_hsa_circ_99898,RMVar_hsa_circ_110144,RMVar_hsa_circ_263368,RMVar_hsa_circ_263369 115377 RMVar_ID_115377 Human_SNP_ID_881532363 m1A Human chrX - 147943328 147943328 147943328 GATAAAGTTACTGAGTAAAATGCTTAGTTTGTACCTGAAGTATATCCAGGACCGCGTCTGCCGTG GATAAAGTTACTGAGTAAAATGCTTAGTTTGTCCCTGAAGTATATCCAGGACCGCGTCTGCCGTG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:147943295..147943380 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115378 RMVar_ID_115378 Human_SNP_ID_881563860 m1A Human chrX + 75274163 75274163 75274163 GCCAGGGTTAGATGTTCTGAGGAGGCGGGAGCAACCGAGAGAGCACGTGAGCATCTGTCCTTTCT GCCAGGGTTAGATGTTCTGAGGAGGCGGGAGCGACCGAGAGAGCACGTGAGCATCTGTCCTTTCT A G UPRT Ensembl:ENSG00000094841 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:75274120..75274277 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - RMVar_hsa_circ_78547,RMVar_hsa_circ_263059 115379 RMVar_ID_115379 Human_SNP_ID_881569674 m1A Human chrX - 74421625 74421625 74421625 GCCTGGCTTTGCAGCGCCATCGCGGCGGGGGGACTGTGGCTGCTTGGGCCAGAGGAGCCGCTTTG GCCTGGCTTTGCAGCGCCATCGCGGCGGGGGGGCTGTGGCTGCTTGGGCCAGAGGAGCCGCTTTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:74421579..74421692 32194978 MeRIP-seq:(Medium) rs1029290713 Functional Loss SNV TCGA,ICGC 33..33 33 COAD,LIHC 3 - 115380 RMVar_ID_115380 Human_SNP_ID_881602673 m1A Human chrX - 154351023 154351023 154351023 TGCTGTGCTTCCAGGAGTCAGGGCTAAAGGTCAACCAGCCAGCCTCTTTTGCAGTCAGCCTGAAC TGCTGTGCTTCCAGGAGTCAGGGCTAAAGGTCGACCAGCCAGCCTCTTTTGCAGTCAGCCTGAAC T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154350863..154351090 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_3918991,Human_RBP_ID_5412550,Human_RBP_ID_9265429,Human_RBP_ID_18197442,Human_RBP_ID_22631469,Human_RBP_ID_22693580,Human_RBP_ID_22748649,Human_RBP_ID_23217326,Human_RBP_ID_26265104,Human_RBP_ID_26835187 Human_Splice_Rec_2247408,Human_Splice_Rec_2247498,Human_Splice_Rec_2247588,Human_Splice_Rec_2247681,Human_Splice_Rec_2247772,Human_Splice_Rec_2247856,Human_Splice_Rec_2247908 Human_miRNA_ID_796026,Human_miRNA_ID_1398221,Human_miRNA_ID_2333833,Human_miRNA_ID_2716926,Human_miRNA_ID_2966918,Human_miRNA_ID_3052908 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_264325 115381 RMVar_ID_115381 Human_SNP_ID_881609143 m1A Human chrX - 101276429 101276424 101276430 TGATGAAGATGAGGATGAGGATGAGGATGAGGATGAAGATGAAGACAAAGAAGAGGAGGAGGAAG TGATGAAGATGAGGATGAGGATGAGGATGAG______GATGAAGACAAAGAAGAGGAGGAGGAAG CTTCATC C TAF7L Ensembl:ENSG00000102387 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:101276389..101276477 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..37 33 LMS 1 - Human_Splice_Rec_2223717,Human_Splice_Rec_2223761 115382 RMVar_ID_115382 Human_SNP_ID_881618081 m1A Human chrX + 12975839 12975839 12975839 TCCTTGCGGAGAGGCCGCGGCTAGGAAATGGAAACGCTTTTCCTACCTGGGCTCCATTTTAGGAA TCCTTGCGGAGAGGCCGCGGCTAGGAAATGGAGACGCTTTTCCTACCTGGGCTCCATTTTAGGAA A G TMSB4X Ensembl:ENSG00000205542 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:12975837..12976300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_79828,RMVar_hsa_circ_261352 115383 RMVar_ID_115383 Human_SNP_ID_881676951 m1A Human chrX - 47224403 47224403 47224403 CCTGGTCACTCTCCCCATCAGACCCCATCTTCAAGTCCTCGTGCACAATCTCTGGTGGCAGGGAG CCTGGTCACTCTCCCCATCAGACCCCATCTTCGAGTCCTCGTGCACAATCTCTGGTGGCAGGGAG T C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:47224401..47224450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115384 RMVar_ID_115384 Human_SNP_ID_881682846 m1A Human chrX - 53216125 53216125 53216125 TGAAAAAGCTACAGATCTATGGGGCAGGCCCCAAGATGATGGGCCTGGGCCTCATGGCCAAAGAC TGAAAAAGCTACAGATCTATGGGGCAGGCCCCGAGATGATGGGCCTGGGCCTCATGGCCAAAGAC T C KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chrX:53216028..53216127;chrX:53215977..53216175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_257347,Human_RBP_ID_966687,Human_RBP_ID_3976552,Human_RBP_ID_5067175,Human_RBP_ID_8936126,Human_RBP_ID_9265279,Human_RBP_ID_9317414,Human_RBP_ID_9409200,Human_RBP_ID_17718476,Human_RBP_ID_18155892,Human_RBP_ID_18921256,Human_RBP_ID_19026679,Human_RBP_ID_26744550,Human_RBP_ID_27834444 Human_Splice_Rec_2208348,Human_Splice_Rec_2208349,Human_Splice_Rec_2208394,Human_Splice_Rec_2208395,Human_Splice_Rec_2208441,Human_Splice_Rec_2208488,Human_Splice_Rec_2208489,Human_Splice_Rec_2208535,Human_Splice_Rec_2208536,Human_Splice_Rec_2208596,Human_Splice_Rec_2208597 RMVar_hsa_circ_107587,RMVar_hsa_circ_262474,RMVar_hsa_circ_87242,RMVar_hsa_circ_262476,RMVar_hsa_circ_265359,RMVar_hsa_circ_118432,RMVar_hsa_circ_61444,RMVar_hsa_circ_262480,RMVar_hsa_circ_262481 115385 RMVar_ID_115385 Human_SNP_ID_881687683 m1A Human chrX - 20141628 20141628 20141628 GCGAGGTCGCCGCCACCGCCATGCCCAAGAATAAAGGTAATGCCGCCCGGACCCCCGGACCACGG GCGAGGTCGCCGCCACCGCCATGCCCAAGAATGAAGGTAATGCCGCCCGGACCCCCGGACCACGG T C EIF1AX Ensembl:ENSG00000173674 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:20141626..20141675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_966234,Human_RBP_ID_19148208 Human_Splice_Rec_2190608,Human_Splice_Rec_2190620 115386 RMVar_ID_115386 Human_SNP_ID_881716558 m1A Human chrX - 9533615 9533615 9533615 TGCTGTCTGCGATAGGTCCCTCTTTGCCTTGGAAATTGTCCTGCCTTCACTTCTCCACAAAGAAA TGCTGTCTGCGATAGGTCCCTCTTTGCCTTGGCAATTGTCCTGCCTTCACTTCTCCACAAAGAAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:9533608..9533810 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 115387 RMVar_ID_115387 Human_SNP_ID_881730586 m1A Human chrX - 153796530 153796530 153796530 ACTGTCTCACCTGGACCCTGTTCTTGCATGTCAGGGAGATCTCCACAATGAAGACGGTCTCAGTG ACTGTCTCACCTGGACCCTGTTCTTGCATGTCGGGGAGATCTCCACAATGAAGACGGTCTCAGTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153796411..153796612 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115388 RMVar_ID_115388 Human_SNP_ID_881735341 m1A Human chrX - 55003110 55003110 55003110 CTCAAGGAAGCCTTACTGCCCAGGCTTGCAGTACCTGCCTGCCGCCAGGAGGGCTTCTGCTCGGA CTCAAGGAAGCCTTACTGCCCAGGCTTGCAGTGCCTGCCTGCCGCCAGGAGGGCTTCTGCTCGGA T C lnc-ALAS2-2 RNACentral:URS0000D5CB50 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:55003076..55003125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115389 RMVar_ID_115389 Human_SNP_ID_881771981 m1A Human chrX - 48944282 48944282 48944282 CCTGTTGCTGACCCCCACCTCTTCCCTCCAGCAGGAGCATTGGTTTGAAAAGGCCCTACGAGACA CCTGTTGCTGACCCCCACCTCTTCCCTCCAGCGGGAGCATTGGTTTGAAAAGGCCCTACGAGACA T C OTUD5 Ensembl:ENSG00000068308 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:48944251..48944300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_735843 Human_Splice_Rec_2204765,Human_Splice_Rec_2204766,Human_Splice_Rec_2204783,Human_Splice_Rec_2204784,Human_Splice_Rec_2204801,Human_Splice_Rec_2204802,Human_Splice_Rec_2204817,Human_Splice_Rec_2204818,Human_Splice_Rec_2204833,Human_Splice_Rec_2204834,Human_Splice_Rec_2204849,Human_Splice_Rec_2204850,Human_Splice_Rec_2204864 RMVar_hsa_circ_291233,RMVar_hsa_circ_262409,RMVar_hsa_circ_112599 115390 RMVar_ID_115390 Human_SNP_ID_881776274 m1A Human chrX - 154461409 154461409 154461409 CAGCCGGCACGCCCAGGGCCTGGGCCAGCAGCAGGCCAGGCTTGGCCAGGTGGGCGCTCTGCACC CAGCCGGCACGCCCAGGGCCTGGGCCAGCAGCCGGCCAGGCTTGGCCAGGTGGGCGCTCTGCACC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154461375..154461526 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 115391 RMVar_ID_115391 Human_SNP_ID_881806704 m1A Human chrX - 119871413 119871413 119871413 GAAAAGAAGCGGGTGACCCACAATCCAATGATACAGAAGACCCGTGACAGTGGTAAACAGAAGGC GAAAAGAAGCGGGTGACCCACAATCCAATGATGCAGAAGACCCGTGACAGTGGTAAACAGAAGGC T C RNF113A Ensembl:ENSG00000125352 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:119871364..119871490 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_17667148,Human_RBP_ID_26364174 115392 RMVar_ID_115392 Human_SNP_ID_881808541 m1A Human chrX - 41341576 41341576 41341576 TGATCCACTTCCACGATCACTGAAGAAGCTAGACTTCCCTCTTGAATCACTACGAGATCCAAAAC TGATCCACTTCCACGATCACTGAAGAAGCTAGGCTTCCCTCTTGAATCACTACGAGATCCAAAAC T C RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:41339050..41341625 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 115393 RMVar_ID_115393 Human_SNP_ID_881812672 m1A Human chrX - 149631723 149631718 149631724 CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA CGGCGGCGGCGGCGGCGGCGACGGCGACGGC______AGCGGGGACGGCAGCAGTAGCGGGAGCA TGCCGTC T TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:149631666..149631782 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..37 33 STAD 1 - Human_RBP_ID_5076791 115394 RMVar_ID_115394 Human_SNP_ID_881831677 m1A Human chrX - 120629992 120629992 120629992 CCTGCAGCTAGAACAGCCTGGTCAGGAGCGTAACGGAGTGGTGCGCCAACGTGAGAGGAAACCCG CCTGCAGCTAGAACAGCCTGGTCAGGAGCGTATCGGAGTGGTGCGCCAACGTGAGAGGAAACCCG T A C1GALT1C1 Ensembl:ENSG00000171155 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:120629882..120630097;chrX:120629887..120630089 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_5076741,Human_RBP_ID_18454020 Human_Splice_Rec_2233033,Human_Splice_Rec_2233035 115395 RMVar_ID_115395 Human_SNP_ID_881832658 m1A Human chrX + 47202449 47202449 47202449 TTCTCGCCCTGCCCAGCTGCACATTGGCTTCCAGGCCCTGCACCAGTTCTGTGCTCAGCATGGCC TTCTCGCCCTGCCCAGCTGCACATTGGCTTCCTGGCCCTGCACCAGTTCTGTGCTCAGCATGGCC A T UBA1 Ensembl:ENSG00000130985 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:47202426..47202450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_93913,Human_RBP_ID_735128,Human_RBP_ID_968598,Human_RBP_ID_3976429,Human_RBP_ID_8719373,Human_RBP_ID_8938630,Human_RBP_ID_9317311,Human_RBP_ID_18920391,Human_RBP_ID_22426756,Human_RBP_ID_22467540,Human_RBP_ID_22778103 Human_Splice_Rec_2201148,Human_Splice_Rec_2201234,Human_Splice_Rec_2201235 Human_miRNA_ID_2575483,Human_miRNA_ID_2921484,Human_miRNA_ID_3005098 RMVar_hsa_circ_20668,RMVar_hsa_circ_90636,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_359980,RMVar_hsa_circ_317621,RMVar_hsa_circ_64133,RMVar_hsa_circ_28136,RMVar_hsa_circ_38306,RMVar_hsa_circ_108583,RMVar_hsa_circ_118943,RMVar_hsa_circ_122703,RMVar_hsa_circ_262254,RMVar_hsa_circ_262255,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_262256,RMVar_hsa_circ_117893,RMVar_hsa_circ_127422,RMVar_hsa_circ_262259,RMVar_hsa_circ_262260,RMVar_hsa_circ_262258,RMVar_hsa_circ_85692,RMVar_hsa_circ_102540,RMVar_hsa_circ_262263,RMVar_hsa_circ_262262,RMVar_hsa_circ_93283,RMVar_hsa_circ_262265,RMVar_hsa_circ_10085,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,RMVar_hsa_circ_262268,RMVar_hsa_circ_266057,RMVar_hsa_circ_106398,RMVar_hsa_circ_116055,RMVar_hsa_circ_85657,RMVar_hsa_circ_262270,RMVar_hsa_circ_262271,RMVar_hsa_circ_262272 115396 RMVar_ID_115396 Human_SNP_ID_881917300 m1A Human chrX - 53595284 53595279 53595285 GCCATCATGCTGCCAGCACCACTACAGCACCGACACCTGCCGCGCGATCAACAGCCTCAGCTCTC GCCATCATGCTGCCAGCACCACTACAGCACC______TGCCGCGCGATCAACAGCCTCAGCTCTC AGGTGTC A HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53595234..53595361 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..37 33 BLCA 1 - Human_RBP_ID_257170,Human_RBP_ID_18197336 Human_Splice_Rec_2209099,Human_Splice_Rec_2209260,Human_Splice_Rec_2209424,Human_Splice_Rec_2209617 RMVar_hsa_circ_490,RMVar_hsa_circ_49196,RMVar_hsa_circ_17855,RMVar_hsa_circ_101893,RMVar_hsa_circ_262559,RMVar_hsa_circ_104969,RMVar_hsa_circ_262560,RMVar_hsa_circ_40553,RMVar_hsa_circ_49868,RMVar_hsa_circ_31413,RMVar_hsa_circ_17816,RMVar_hsa_circ_353177,RMVar_hsa_circ_283377,RMVar_hsa_circ_361861,RMVar_hsa_circ_269687,RMVar_hsa_circ_306741 115397 RMVar_ID_115397 Human_SNP_ID_881923542 m1A Human chrX + 149938420 149938420 149938420 CCGCTTACTCCCGGAAACCGGTGGCCAGTGACAGATGCTAGCGGTCCATAACTTCGGCTTTCATG CCGCTTACTCCCGGAAACCGGTGGCCAGTGACCGATGCTAGCGGTCCATAACTTCGGCTTTCATG A C LINC00894,LINC00894:2 RNACentral:URS00008BDAE6,RNACentral:URS00009B7AC8 lincRNA,lincRNA exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:149938358..149938430 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115398 RMVar_ID_115398 Human_SNP_ID_881951383 m1A Human chrX + 65534637 65534637 65534637 CGAGAGTGGCAACGACCCTTTCCCTTTAACGCACTTTCCGTACCACGCACTCCACACGAGATCCA CGAGAGTGGCAACGACCCTTTCCCTTTAACGCTCTTTCCGTACCACGCACTCCACACGAGATCCA A T lnc-ZC3H12B-2 RNACentral:URS00008B38C1 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:65534589..65534800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 READ 1 - 115399 RMVar_ID_115399 Human_SNP_ID_881958861 m1A Human chrX - 53539735 53539735 53539735 CACCTGAGTTACCCCTGCTCAGCGAGCAGCTGAGTTTGGACGAGCTGTGGGACATGCTTGGGGAG CACCTGAGTTACCCCTGCTCAGCGAGCAGCTGTGTTTGGACGAGCTGTGGGACATGCTTGGGGAG T A HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53539625..53539734 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_93100,Human_RBP_ID_2075805,Human_RBP_ID_8009281,Human_RBP_ID_8936433,Human_RBP_ID_19026682,Human_RBP_ID_23107644,Human_RBP_ID_24346629 Human_Splice_Rec_2209028,Human_Splice_Rec_2209029,Human_Splice_Rec_2209185,Human_Splice_Rec_2209186,Human_Splice_Rec_2209347,Human_Splice_Rec_2209348,Human_Splice_Rec_2209512,Human_Splice_Rec_2209513,Human_Splice_Rec_2209538 RMVar_hsa_circ_108436,RMVar_hsa_circ_262504,RMVar_hsa_circ_84205,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_117713,RMVar_hsa_circ_98834,RMVar_hsa_circ_262506,RMVar_hsa_circ_262508,RMVar_hsa_circ_92009,RMVar_hsa_circ_262509,RMVar_hsa_circ_114735,RMVar_hsa_circ_363826,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262511,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_50358,RMVar_hsa_circ_87804,RMVar_hsa_circ_91628,RMVar_hsa_circ_262518,RMVar_hsa_circ_262520,RMVar_hsa_circ_85924,RMVar_hsa_circ_262519,RMVar_hsa_circ_262517,RMVar_hsa_circ_335666 115400 RMVar_ID_115400 Human_SNP_ID_881993697 m1A Human chrX + 21940776 21940776 21940776 CGGCCGCAGCCTGACACGCCGCGCGGCCCCCCAGTCTCCCGCGGCTGCTCCCCCAGGCATGGCAC CGGCCGCAGCCTGACACGCCGCGCGGCCCCCCCGTCTCCCGCGGCTGCTCCCCCAGGCATGGCAC A C SMS Ensembl:ENSG00000102172 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:21940726..21940879 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_5060393,Human_RBP_ID_8938565,Human_RBP_ID_26834587 Human_Splice_Rec_2192317,Human_Splice_Rec_2192335,Human_Splice_Rec_2192349 Human_miRNA_ID_3011898,Human_miRNA_ID_3086967 RMVar_hsa_circ_104311,RMVar_hsa_circ_261729 115401 RMVar_ID_115401 Human_SNP_ID_882010442 m1A Human chrX - 154376878 154376878 154376878 GGAATTCTAGATTTGCCTTCTCCCTAAGGAGCACCCCCCACCCGTTCTGTACCTGCCTCGACACT GGAATTCTAGATTTGCCTTCTCCCTAAGGAGCCCCCCCCACCCGTTCTGTACCTGCCTCGACACT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154376829..154377042 26863196 MeRIP-seq:(Medium) rs1557181655 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115402 RMVar_ID_115402 Human_SNP_ID_882023213 m1A Human chrX - 103676990 103676990 103676990 TTCCAGAAAGCAGGGTTCTCAACCTCGTGGACAGCAATCTGCAGAAGAAGAGAACTTCAAAAAAC TTCCAGAAAGCAGGGTTCTCAACCTCGTGGACGGCAATCTGCAGAAGAAGAGAACTTCAAAAAAC T C MORF4L2 Ensembl:ENSG00000123562 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_93647,Human_RBP_ID_287521,Human_RBP_ID_724358,Human_RBP_ID_968221,Human_RBP_ID_1709547,Human_RBP_ID_2068163,Human_RBP_ID_5535762,Human_RBP_ID_7962390,Human_RBP_ID_8710431,Human_RBP_ID_9241715,Human_RBP_ID_9409432,Human_RBP_ID_16779806,Human_RBP_ID_17551882,Human_RBP_ID_17717327,Human_RBP_ID_18453921,Human_RBP_ID_22468924,Human_RBP_ID_22840134,Human_RBP_ID_23117414,Human_RBP_ID_24320059,Human_RBP_ID_24550054,Human_RBP_ID_26363226,Human_RBP_ID_27378053,Human_RBP_ID_27548905,Human_RBP_ID_27834667 Human_Splice_Rec_2225957,Human_Splice_Rec_2225962,Human_Splice_Rec_2225971,Human_Splice_Rec_2225977,Human_Splice_Rec_2225985,Human_Splice_Rec_2225993,Human_Splice_Rec_2226010,Human_Splice_Rec_2226014,Human_Splice_Rec_2226020,Human_Splice_Rec_2226026 RMVar_hsa_circ_89385,RMVar_hsa_circ_377960,RMVar_hsa_circ_263380,RMVar_hsa_circ_263381 115403 RMVar_ID_115403 Human_SNP_ID_882024201 m1A Human chrX - 154351028 154351028 154351028 ATGTCTGCTGTGCTTCCAGGAGTCAGGGCTAAAGGTCAACCAGCCAGCCTCTTTTGCAGTCAGCC ATGTCTGCTGTGCTTCCAGGAGTCAGGGCTAAGGGTCAACCAGCCAGCCTCTTTTGCAGTCAGCC T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154350853..154351083 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_5412550,Human_RBP_ID_18197669,Human_RBP_ID_22557170,Human_RBP_ID_22631469,Human_RBP_ID_22693580,Human_RBP_ID_22748649,Human_RBP_ID_26265104 Human_Splice_Rec_2247408,Human_Splice_Rec_2247498,Human_Splice_Rec_2247588,Human_Splice_Rec_2247681,Human_Splice_Rec_2247772,Human_Splice_Rec_2247856,Human_Splice_Rec_2247908 Human_miRNA_ID_796026,Human_miRNA_ID_1398221,Human_miRNA_ID_2333833,Human_miRNA_ID_2716926,Human_miRNA_ID_2966918,Human_miRNA_ID_3052908 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_264325 115404 RMVar_ID_115404 Human_SNP_ID_882044919 m1A Human chrX + 103609514 103609514 103609514 ATGAGAGAATGTGGAGATGTGTCAAGGGCTCAAGAGGAGCTAAGGAAAAAACAGAAAATGGGTGG ATGAGAGAATGTGGAGATGTGTCAAGGGCTCAGGAGGAGCTAAGGAAAAAACAGAAAATGGGTGG A G TCEAL3 Ensembl:ENSG00000196507 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:103609418..103609517 32194978 MeRIP-seq:(Medium) rs780244651 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1060241,Human_RBP_ID_24319988 115405 RMVar_ID_115405 Human_SNP_ID_882056160 m1A Human chrX + 53564665 53564665 53564665 CAGCCTCCCCATCCATGATATCCCCATCTGCCACCTCTGTCTGAGTGACATCATGATCCTCCTCC CAGCCTCCCCATCCATGATATCCCCATCTGCCCCCTCTGTCTGAGTGACATCATGATCCTCCTCC A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:53564575..53564717 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ACC 1 - 115406 RMVar_ID_115406 Human_SNP_ID_882061472 m1A Human chrX + 12975481 12975481 12975481 GTGCGTTGCCTTGGAGGCTGAGATATGGGGGAATAGACAAGTCCTTTGTTCTGAGGTTCATCTTC GTGCGTTGCCTTGGAGGCTGAGATATGGGGGAGTAGACAAGTCCTTTGTTCTGAGGTTCATCTTC A G TMSB4X Ensembl:ENSG00000205542 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:12975476..12975877 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_8712931 RMVar_hsa_circ_79828,RMVar_hsa_circ_261352 115407 RMVar_ID_115407 Human_SNP_ID_882062111 m1A Human chrX - 54444118 54444118 54444118 TCCTCATCAGTCTCTCTAGCTGTCTTAAGTGCAGTGGCTGTGACCTTGCATTTTCTCTGAGTGAT TCCTCATCAGTCTCTCTAGCTGTCTTAAGTGCGGTGGCTGTGACCTTGCATTTTCTCTGAGTGAT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chrX:54444068..54444641;chrX:54440499..54444498 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115408 RMVar_ID_115408 Human_SNP_ID_882072961 m1A Human chrX + 72186533 72186533 72186533 TCAAGGTCCCAAAGGTGGTGGCAATGCAGTAAAGGTGAGTTACTGGTTCCTTTTTTTCCATGTTA TCAAGGTCCCAAAGGTGGTGGCAATGCAGTAAGGGTGAGTTACTGGTTCCTTTTTTTCCATGTTA A G PIN4 Ensembl:ENSG00000102309 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:72186501..72186550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_5155322 Human_Splice_Rec_2216933,Human_Splice_Rec_2216936,Human_Splice_Rec_2216937,Human_Splice_Rec_2216940,Human_Splice_Rec_2216941,Human_Splice_Rec_2216946,Human_Splice_Rec_2216947,Human_Splice_Rec_2216952,Human_Splice_Rec_2216953,Human_Splice_Rec_2216958,Human_Splice_Rec_2216959,Human_Splice_Rec_2216964,Human_Splice_Rec_2216965,Human_Splice_Rec_2216970,Human_Splice_Rec_2216971,Human_Splice_Rec_2216980,Human_Splice_Rec_2216981 RMVar_hsa_circ_70826 115409 RMVar_ID_115409 Human_SNP_ID_882077188 m1A Human chrX - 101616502 101616502 101616502 AGGAAGAGATGACAGTGAGAAGCTGGAGGAGGAGGGGGAAGAGGAGTGGGACGATGACCAGGAGC AGGAAGAGATGACAGTGAGAAGCTGGAGGAGGGGGGGGAAGAGGAGTGGGACGATGACCAGGAGC T C ARMCX6 Ensembl:ENSG00000198960 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:101616411..101616611 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD,STAD 2 - Human_RBP_ID_7961226,Human_RBP_ID_24319105 115410 RMVar_ID_115410 Human_SNP_ID_882083830 m1A Human chrX - 149631723 149631723 149631723 CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGACGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA CGGCGGCGGCGGCGGCGGCGACGGCGACGGCGGCGGCAGCGGGGACGGCAGCAGTAGCGGGAGCA T C TMEM185A Ensembl:ENSG00000269556 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:149631666..149631782 26863410 MeRIP-seq:(Medium) rs868927082 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_5076791 115411 RMVar_ID_115411 Human_SNP_ID_882116768 m1A Human chrX - 129654907 129654907 129654907 GCCGGGGTCACGGGCAGTTGCAGCCGCGGCCGAGCAGCCAGCCGCTAAGAAAGAGCTCGCCGCTG GCCGGGGTCACGGGCAGTTGCAGCCGCGGCCGTGCAGCCAGCCGCTAAGAAAGAGCTCGCCGCTG T A APLN Ensembl:ENSG00000171388 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:129654858..129654923 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_117424,RMVar_hsa_circ_263838 115412 RMVar_ID_115412 Human_SNP_ID_882138128 m1A Human chrX - 30218606 30218606 30218606 CTCGGGCCTTGCGGCGTTTCTCACGGGCACGGAGCTTACTCTTCTGACCACGAGGCATGATGGCT CTCGGGCCTTGCGGCGTTTCTCACGGGCACGGTGCTTACTCTTCTGACCACGAGGCATGATGGCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:30215576..30218650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 115413 RMVar_ID_115413 Human_SNP_ID_882167702 m1A Human chrX + 17388601 17388600 17388601 AGGCCAGGGTGGTGGATGAGGAGTTAGCAAGGAGGAGAGTAGGAGGATAAGAGGCCAGCAAGGAG AGGCCAGGGTGGTGGATGAGGAGTTAGCAAGG_GGAGAGTAGGAGGATAAGAGGCCAGCAAGGAG GA G NHS Ensembl:ENSG00000188158 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:17388360..17388739;chrX:17388377..17388647 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 115414 RMVar_ID_115414 Human_SNP_ID_882175437 m1A Human chrX - 92113718 92113718 92113718 AAGGAAGAGTTGACCCTGGAGGGTATCCGCCAATTCTACATCAACGTGGAACGAGAGGAGTGGAA AAGGAAGAGTTGACCCTGGAGGGTATCCGCCAGTTCTACATCAACGTGGAACGAGAGGAGTGGAA T C EIF4A1P10 Ensembl:ENSG00000229132 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879093645 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5637984,Human_RBP_ID_18522295,Human_RBP_ID_22413482 115415 RMVar_ID_115415 Human_SNP_ID_882195032 m1A Human chrX - 10116442 10116442 10116442 CGGGTGGCTTCTTCCAGCTGCATAAGTAGACAATTCCTTTTTTCCTGAAGCAGAATCCTGTAGGT CGGGTGGCTTCTTCCAGCTGCATAAGTAGACAGTTCCTTTTTTCCTGAAGCAGAATCCTGTAGGT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:10116373..10116441 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115416 RMVar_ID_115416 Human_SNP_ID_882223015 m1A Human chrX - 119838001 119838001 119838001 CAGAGACTATAGGGAGAGGGAACGGGAATATGAACGAGATCAGGAGCGCATACTTCGAGAAAGAG CAGAGACTATAGGGAGAGGGAACGGGAATATGTACGAGATCAGGAGCGCATACTTCGAGAAAGAG T A UPF3B Ensembl:ENSG00000125351 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:119834926..119843194 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_257325,Human_RBP_ID_287572,Human_RBP_ID_849009,Human_RBP_ID_1060742,Human_RBP_ID_3977623,Human_RBP_ID_16803655,Human_RBP_ID_19148582,Human_RBP_ID_24549979,Human_RBP_ID_26364166,Human_RBP_ID_27834085 Human_Splice_Rec_2232358,Human_Splice_Rec_2232376 RMVar_hsa_circ_77325,RMVar_hsa_circ_100356,RMVar_hsa_circ_109896,RMVar_hsa_circ_120482,RMVar_hsa_circ_84898,RMVar_hsa_circ_263664,RMVar_hsa_circ_263666,RMVar_hsa_circ_263667,RMVar_hsa_circ_263668,RMVar_hsa_circ_263665,RMVar_hsa_circ_263669,RMVar_hsa_circ_326529 115417 RMVar_ID_115417 Human_SNP_ID_882240537 m1A Human chrX + 154380787 154380787 154380787 GCATGATGACGATCTTTTGTCTTCTTCTGAAGAGGAGTGCAAGGATAGGTGCGTAGTGGGGGAGC GCATGATGACGATCTTTTGTCTTCTTCTGAAGGGGAGTGCAAGGATAGGTGCGTAGTGGGGGAGC A G EMD Ensembl:ENSG00000102119 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154380751..154380825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_93513,Human_RBP_ID_731659,Human_RBP_ID_799288,Human_RBP_ID_1712572,Human_RBP_ID_9244879,Human_RBP_ID_9410225,Human_RBP_ID_18917351 Human_Splice_Rec_2247976,Human_Splice_Rec_2247977,Human_Splice_Rec_2247986,Human_Splice_Rec_2247987,Human_Splice_Rec_2247994,Human_Splice_Rec_2248002,Human_Splice_Rec_2248003,Human_Splice_Rec_2248008,Human_Splice_Rec_2248019,Human_Splice_Rec_2248025,Human_Splice_Rec_2248026,Human_Splice_Rec_2248028 Human_miRNA_ID_2490990,Human_miRNA_ID_2709448,Human_miRNA_ID_2753079 RMVar_hsa_circ_127590,RMVar_hsa_circ_79186,RMVar_hsa_circ_77652,RMVar_hsa_circ_264490,RMVar_hsa_circ_123092,RMVar_hsa_circ_264491,RMVar_hsa_circ_264492,RMVar_hsa_circ_264493 115418 RMVar_ID_115418 Human_SNP_ID_882243343 m1A Human chrX - 65739926 65739926 65739926 AGTTAGGTGTAGGAGTGTGGGGACAAGGAAAAAGGGAGGAGGGGTCCCTAGAGGCTGGGTGCCCA AGTTAGGTGTAGGAGTGTGGGGACAAGGAAAAGGGGAGGAGGGGTCCCTAGAGGCTGGGTGCCCA T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:65739876..65740075 26863196 MeRIP-seq:(Medium) rs1295199712 Functional Loss SNV TCGA 33..33 33 CESC,LUAD 2 - 115419 RMVar_ID_115419 Human_SNP_ID_882274984 m1A Human chrX + 70407041 70407041 70407041 TGAGGGGGATGACGAGGAATGGAAGCCAACAAAATTAGTTAAGGTGTCCAGGAAGAACATCCAAG TGAGGGGGATGACGAGGAATGGAAGCCAACAACATTAGTTAAGGTGTCCAGGAAGAACATCCAAG A C KIF4A Ensembl:ENSG00000090889 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:70406940..70407040 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_8937067 Human_Splice_Rec_2214292 RMVar_hsa_circ_100960,RMVar_hsa_circ_262861,RMVar_hsa_circ_89286,RMVar_hsa_circ_262867,RMVar_hsa_circ_262868,RMVar_hsa_circ_277862 115420 RMVar_ID_115420 Human_SNP_ID_882289590 m1A Human chrX + 53625853 53625841 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCG____________GGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG GGGGCCGGGGCCA G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs782399689 Functional Loss DEL TCGA 22..33 33 ESCA 1 - 115421 RMVar_ID_115421 Human_SNP_ID_882308278 m1A Human chrX - 1593797 1593797 1593797 TGGGGAAGTCGATCTTGAACTCGGCCGCGCGCACCTTCAGGATGTCGGAGAAGCCGCTGAGCTTG TGGGGAAGTCGATCTTGAACTCGGCCGCGCGCCCCTTCAGGATGTCGGAGAAGCCGCTGAGCTTG T G RF00017-4643,RF00017-4501 RNACentral:URS00009A02E8,RNACentral:URS0000972B66 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:1593751..1594051 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 115422 RMVar_ID_115422 Human_SNP_ID_882361195 m1A Human chrX + 154508540 154508539 154508540 CGTTGGCGGCCCCGCTGACCACGCGGAAGGCCAGGTGCTCCTCAGGACACGGCTGGGGCAGGCCA CGTTGGCGGCCCCGCTGACCACGCGGAAGGCC_GGTGCTCCTCAGGACACGGCTGGGGCAGGCCA CA C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:154508297..154508653 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 115423 RMVar_ID_115423 Human_SNP_ID_882376621 m1A Human chrX + 153870466 153870466 153870466 CCACCAGGTGGCTGCTGGAGTTGGTGGGGAAGAGCAGGCGCGGCTTCCTGTCAATCATGCTGTTG CCACCAGGTGGCTGCTGGAGTTGGTGGGGAAGCGCAGGCGCGGCTTCCTGTCAATCATGCTGTTG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:153870426..153870500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUAD 1 - 115424 RMVar_ID_115424 Human_SNP_ID_882404480 m1A Human chrX - 41341585 41341553 41341585 CCTTCCCCTTGATCCACTTCCACGATCACTGAAGAAGCTAGACTTCCCTCTTGAATCACTACGAG CCTTCCCCTTGATCCACTTCCACGATCACTGA________________________________G CTCGTAGTGATTCAAGAGGGAAGTCTAGCTTCT C RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:41341534..41341645 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..64 33 LICA 1 - 115425 RMVar_ID_115425 Human_SNP_ID_882411260 m1A Human chrX - 135051967 135051967 135051967 CCGACCGACTCCCGGAGTTCATCGTGCAGACGAGCTCCTACATGTTCGTGGACGAGAACACGTTC CCGACCGACTCCCGGAGTTCATCGTGCAGACGTGCTCCTACATGTTCGTGGACGAGAACACGTTC T A RTL8A Ensembl:ENSG00000203950 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2498776 Functional Loss SNV ICGC 33..33 33 COCA 2 - Human_Splice_Rec_2237551,Human_Splice_Rec_2237553,Human_Splice_Rec_2237555 115426 RMVar_ID_115426 Human_SNP_ID_882440366 m1A Human chrX - 115543875 115543874 115543876 ACAAAGAGGGAGTCAAGGAGAGAGAGAGAGAGAAAAAGAAAGAGAGAGGCAGAGAGAGAGAAGAA ACAAAGAGGGAGTCAAGGAGAGAGAGAGAGA__AAAAGAAAGAGAGAGGCAGAGAGAGAGAAGAA TTC T PLS3-AS1 Ensembl:ENSG00000271826 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:115543827..115543939 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 PRAD 1 - 115427 RMVar_ID_115427 Human_SNP_ID_882442510 m1A Human chrX - 136880667 136880667 136880667 TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCACTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC TCGCGGTTCGGTCCTCGCACCCGGCAGCCGCCTCTGGTGCTGAGCTGCTAGGAAGCCCCTATCGC T A RBMX Ensembl:ENSG00000147274 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:136880542..136880725 26863196 MeRIP-seq:(Medium) rs1243195018 Functional Loss SNV TCGA 33..33 33 CESC 1 - Human_RBP_ID_729677,Human_RBP_ID_5054212,Human_RBP_ID_5431932,Human_RBP_ID_18428060,Human_RBP_ID_18916152,Human_RBP_ID_22468993,Human_RBP_ID_24331363,Human_RBP_ID_27379648 Human_Splice_Rec_2239308,Human_Splice_Rec_2239326,Human_Splice_Rec_2239354,Human_Splice_Rec_2239368,Human_Splice_Rec_2239384,Human_Splice_Rec_2239398,Human_Splice_Rec_2239410,Human_Splice_Rec_2239418,Human_Splice_Rec_2239424 115428 RMVar_ID_115428 Human_SNP_ID_882461965 m1A Human chrX - 53547748 53547748 53547748 CTGTCACTTCTGCTCCAGCCCTGGTTGCTGCCACGGCTATTTCCACCATTGTCGTAGCTGCTTCG CTGTCACTTCTGCTCCAGCCCTGGTTGCTGCCGCGGCTATTTCCACCATTGTCGTAGCTGCTTCG T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:53547726..53547750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_93116,Human_RBP_ID_257153,Human_RBP_ID_8720345,Human_RBP_ID_8936476,Human_RBP_ID_9317958,Human_RBP_ID_17096248,Human_RBP_ID_17326659,Human_RBP_ID_17442722,Human_RBP_ID_17554890,Human_RBP_ID_18963979,Human_RBP_ID_22122809,Human_RBP_ID_22348460,Human_RBP_ID_22467637,Human_RBP_ID_23108764,Human_RBP_ID_26834808 Human_Splice_Rec_2209015,Human_Splice_Rec_2209172,Human_Splice_Rec_2209334,Human_Splice_Rec_2209499,Human_Splice_Rec_2209539,Human_Splice_Rec_2209549 Human_miRNA_ID_2027750 RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_121389,RMVar_hsa_circ_262503,RMVar_hsa_circ_262505,RMVar_hsa_circ_75758,RMVar_hsa_circ_95414,RMVar_hsa_circ_76461,RMVar_hsa_circ_99884,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_81801,RMVar_hsa_circ_262514,RMVar_hsa_circ_262515,RMVar_hsa_circ_262516,RMVar_hsa_circ_262513,RMVar_hsa_circ_91628,RMVar_hsa_circ_262520,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_262523,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_79230,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_80577,RMVar_hsa_circ_113187,RMVar_hsa_circ_262529,RMVar_hsa_circ_99745,RMVar_hsa_circ_262530,RMVar_hsa_circ_262531,RMVar_hsa_circ_127894,RMVar_hsa_circ_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_18327,RMVar_hsa_circ_262535,RMVar_hsa_circ_262533 115429 RMVar_ID_115429 Human_SNP_ID_882468505 m1A Human chrX - 74583048 74583048 74583048 CAGGGACCACGAAAAGAAACTTGTGCTTCACCAAAGAAAAATATCTAAACATCGAAAAACTTAAA CAGGGACCACGAAAAGAAACTTGTGCTTCACCGAAGAAAAATATCTAAACATCGAAAAACTTAAA T C RLIM Ensembl:ENSG00000131263 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879222169 Functional Loss SNV ICGC 33..33 33 LAML 2 - 115430 RMVar_ID_115430 Human_SNP_ID_882480700 m1A Human chrX - 53082978 53082978 53082978 ATGATGATCGCCTCTTCCTTGCTCTTCGGGTCAACTAACCTCTGGGGCGCCCACCCCACTGCGCT ATGATGATCGCCTCTTCCTTGCTCTTCGGGTCTACTAACCTCTGGGGCGCCCACCCCACTGCGCT T A lnc-FAM156A-2 RNACentral:URS00008B9BC0 lincRNA exon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:53082926..53083087 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SARC 1 - 115431 RMVar_ID_115431 Human_SNP_ID_882489579 m1A Human chrX + 119943374 119943369 119943375 CCGGGGCGCAGAGGGCCGCTCTCTAGAACGCGACCGCGAGCGTGAGCGGTAGGACTGGTTTCGGG CCGGGGCGCAGAGGGCCGCTCTCTAGAA______CGCGAGCGTGAGCGGTAGGACTGGTTTCGGG ACGCGAC A RHOXF1P3 Ensembl:ENSG00000282933 Pseudogene exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:119943327..119943575 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 29..34 33 HNSC 1 - 115432 RMVar_ID_115432 Human_SNP_ID_882499809 m1A Human chrX + 47226699 47226699 47226699 TTGGGTCCACGGACTACTCCACTCAGATTGACATGTGGTAAGGACAGGTGGAAGTGTGGCAGGGG TTGGGTCCACGGACTACTCCACTCAGATTGACCTGTGGTAAGGACAGGTGGAAGTGTGGCAGGGG A C CDK16 Ensembl:ENSG00000102225 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:47226601..47226725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_19027256 Human_Splice_Rec_2201376,Human_Splice_Rec_2201422,Human_Splice_Rec_2201452,Human_Splice_Rec_2201492,Human_Splice_Rec_2201518,Human_Splice_Rec_2201548,Human_Splice_Rec_2201572,Human_Splice_Rec_2201586,Human_Splice_Rec_2201592 RMVar_hsa_circ_115498,RMVar_hsa_circ_54231,RMVar_hsa_circ_262291,RMVar_hsa_circ_311251,RMVar_hsa_circ_114371,RMVar_hsa_circ_82865,RMVar_hsa_circ_23084,RMVar_hsa_circ_262295,RMVar_hsa_circ_262296,RMVar_hsa_circ_262294,RMVar_hsa_circ_262297,RMVar_hsa_circ_364185,RMVar_hsa_circ_33920,RMVar_hsa_circ_354178,RMVar_hsa_circ_262299,RMVar_hsa_circ_342597 115433 RMVar_ID_115433 Human_SNP_ID_882503916 m1A Human chrX - 19706930 19706930 19706930 CCAGGTGGCATTCAGCTACCTGCCCCAGAATGACGATGAACTTGAGCTGAAAGTTGGCGACATCA CCAGGTGGCATTCAGCTACCTGCCCCAGAATGGCGATGAACTTGAGCTGAAAGTTGGCGACATCA T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chrX:19706851..19706942 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_5060027,Human_RBP_ID_7991484 Human_Splice_Rec_2190219,Human_Splice_Rec_2190220,Human_Splice_Rec_2190274,Human_Splice_Rec_2190275,Human_Splice_Rec_2190303,Human_Splice_Rec_2190304,Human_Splice_Rec_2190341,Human_Splice_Rec_2190342,Human_Splice_Rec_2190387,Human_Splice_Rec_2190388,Human_Splice_Rec_2190395,Human_Splice_Rec_2190396 RMVar_hsa_circ_64731,RMVar_hsa_circ_261629,RMVar_hsa_circ_112181,RMVar_hsa_circ_83738,RMVar_hsa_circ_261624,RMVar_hsa_circ_261625,RMVar_hsa_circ_366222,RMVar_hsa_circ_73955,RMVar_hsa_circ_360809,RMVar_hsa_circ_320029,RMVar_hsa_circ_59312,RMVar_hsa_circ_44711,RMVar_hsa_circ_283375,RMVar_hsa_circ_309576,RMVar_hsa_circ_310490,RMVar_hsa_circ_261627,RMVar_hsa_circ_261628,RMVar_hsa_circ_261631,RMVar_hsa_circ_303061,RMVar_hsa_circ_337027,RMVar_hsa_circ_291076,RMVar_hsa_circ_261630,RMVar_hsa_circ_296730,RMVar_hsa_circ_340273 115434 RMVar_ID_115434 Human_SNP_ID_882514843 m1A Human chrX - 47233076 47233076 47233076 GTCACCGCCGCTGCCGCCGCCACAGCCGCCGCAGCAGCAGCTGGATTTGCTGCGACCGTCGCCAT GTCACCGCCGCTGCCGCCGCCACAGCCGCCGCCGCAGCAGCTGGATTTGCTGCGACCGTCGCCAT T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:47233026..47233200;chrX:47233026..47233272;chrX:47233026..47233267 26863196 MeRIP-seq:(Medium) rs918867462 Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - 115435 RMVar_ID_115435 Human_SNP_ID_882517948 m1A Human chrX - 49247720 49247720 49247720 CCCAGGGTCTTCATGTCGGCCTCAACCTCCTCAATGCTGCGGTTCACTCCTTCCAGCTGCTCCCG CCCAGGGTCTTCATGTCGGCCTCAACCTCCTCGATGCTGCGGTTCACTCCTTCCAGCTGCTCCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:49247670..49247744 26863196 MeRIP-seq:(Medium) rs782294044 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115436 RMVar_ID_115436 Human_SNP_ID_882555465 m1A Human chrX + 21839787 21839787 21839787 GGTGGTGGTGGTGGGTGGCTGGACTGTCGTCTACCTGACCGACTTGGTGCTGAAGGTGAGGGCCT GGTGGTGGTGGTGGGTGGCTGGACTGTCGTCTTCCTGACCGACTTGGTGCTGAAGGTGAGGGCCT A T MBTPS2 Ensembl:ENSG00000012174 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:21839624..21839866 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_5075764,Human_RBP_ID_24337834 Human_Splice_Rec_2192275,Human_Splice_Rec_2192295,Human_Splice_Rec_2192305 115437 RMVar_ID_115437 Human_SNP_ID_882581733 m1A Human chrX + 20266750 20266750 20266750 ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC ACGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCAGCGGCAGCAGCAGCAGCAGC A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:20266703..20266910 26863196 MeRIP-seq:(Medium) rs12396661 Functional Loss SNV ICGC 33..33 33 CHOL 2 - 115438 RMVar_ID_115438 Human_SNP_ID_882586248 m1A Human chrX + 23667625 23667612 23667625 CCGCGACAACTCCGGACCACGGCCGCCACCGAAGGCTGCTTCTGCTGCCGCTACTGCTGTTCCTG CCGCGACAACTCCGGACCAC_____________GGCTGCTTCTGCTGCCGCTACTGCTGTTCCTG CGGCCGCCACCGAA C PRDX4 Ensembl:ENSG00000123131 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:23667525..23667850 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 21..33 33 LUSC 1 - Human_RBP_ID_257297,Human_RBP_ID_733353,Human_RBP_ID_1713629,Human_RBP_ID_5060447,Human_RBP_ID_9339891,Human_RBP_ID_22468253,Human_RBP_ID_24338053,Human_RBP_ID_27551257 RMVar_hsa_circ_102679,RMVar_hsa_circ_261762 115439 RMVar_ID_115439 Human_SNP_ID_882595411 m1A Human chrX - 1395786 1395786 1395786 TCCATCCATCCATCCATCATCCATCCATCTATACATTATCCATCCATCTATCCATTATCCATCCA TCCATCCATCCATCCATCATCCATCCATCTATCCATTATCCATCCATCTATCCATTATCCATCCA T G RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:1395735..1395898 26863196 MeRIP-seq:(Medium) rs868651537 Functional Loss SNV ICGC 33..33 33 MALY 2 - 115440 RMVar_ID_115440 Human_SNP_ID_882604721 m1A Human chrX + 153794319 153794319 153794319 TCGCGGCGCTGCCGGCGACGGTCGCTACCTTCAGCGCCATGACGGAAAGTGAGAGCCTCCGCACG TCGCGGCGCTGCCGGCGACGGTCGCTACCTTCGGCGCCATGACGGAAAGTGAGAGCCTCCGCACG A G SSR4 Ensembl:ENSG00000180879 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153794117..153794375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 KIRC 2 - Human_Splice_Rec_2245499,Human_Splice_Rec_2245503 115441 RMVar_ID_115441 Human_SNP_ID_882622186 m1A Human chrX + 150985689 150985689 150985689 GTGCAGACATGCAGAGAAGAACATAAGAAGAAAAACCCAGAGGTCCCTGTCAATTTTGCGGAATT GTGCAGACATGCAGAGAAGAACATAAGAAGAACAACCCAGAGGTCCCTGTCAATTTTGCGGAATT A C HMGB3 Ensembl:ENSG00000029993 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:150985576..150985775 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_9409549 Human_Splice_Rec_2242573,Human_Splice_Rec_2242574,Human_Splice_Rec_2242581,Human_Splice_Rec_2242582,Human_Splice_Rec_2242589,Human_Splice_Rec_2242590,Human_Splice_Rec_2242597,Human_Splice_Rec_2242598,Human_Splice_Rec_2242604 Human_miRNA_ID_2426047,Human_miRNA_ID_2435717 RMVar_hsa_circ_9387,RMVar_hsa_circ_103141,RMVar_hsa_circ_86790,RMVar_hsa_circ_264140,RMVar_hsa_circ_264141 115442 RMVar_ID_115442 Human_SNP_ID_882633643 m1A Human chrX + 100822320 100822320 100822320 TATGGCTTCTGTGAATACCAAGACCAAGAGACAGCACTTAGTGCCATGCGGAACCTGAATGGGCG TATGGCTTCTGTGAATACCAAGACCAAGAGACGGCACTTAGTGCCATGCGGAACCTGAATGGGCG A G CSTF2 Ensembl:ENSG00000101811 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:100821512..100822425;chrX:100822225..100822375 26863196 MeRIP-seq:(Medium) rs778016639 Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_723564,Human_RBP_ID_968414,Human_RBP_ID_16772067 Human_Splice_Rec_2223046,Human_Splice_Rec_2223073,Human_Splice_Rec_2223098,Human_Splice_Rec_2223123 Human_miRNA_ID_2134777,Human_miRNA_ID_2317190,Human_miRNA_ID_2320345,Human_miRNA_ID_2323499,Human_miRNA_ID_2326675,Human_miRNA_ID_2329760,Human_miRNA_ID_2521052,Human_miRNA_ID_2524220,Human_miRNA_ID_2776075,Human_miRNA_ID_2823400,Human_miRNA_ID_2829531,Human_miRNA_ID_2832688,Human_miRNA_ID_2836815,Human_miRNA_ID_2842163 RMVar_hsa_circ_98233,RMVar_hsa_circ_263264 115443 RMVar_ID_115443 Human_SNP_ID_882636163 m1A Human chrX + 147912135 147912135 147912135 GGCGGCGGCTGGGCCTCGAGCGCCCGCAGCCCACCTCTCGGGGGCGGGCTCCCGGCGCTAGCAGG GGCGGCGGCTGGGCCTCGAGCGCCCGCAGCCCTCCTCTCGGGGGCGGGCTCCCGGCGCTAGCAGG A T FMR1 Ensembl:ENSG00000102081 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:147911946..147912200 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_19027678,Human_RBP_ID_22468560 Human_Splice_Rec_2240689,Human_Splice_Rec_2240721,Human_Splice_Rec_2240748,Human_Splice_Rec_2240778,Human_Splice_Rec_2240807,Human_Splice_Rec_2240837,Human_Splice_Rec_2240859,Human_Splice_Rec_2240889,Human_Splice_Rec_2240907,Human_Splice_Rec_2240925,Human_Splice_Rec_2240955,Human_Splice_Rec_2240981,Human_Splice_Rec_2240983,Human_Splice_Rec_2240996 115444 RMVar_ID_115444 Human_SNP_ID_882675111 m1A Human chrX + 68838769 68838769 68838769 TGAGCAGGCAGCTGCCTGTAGCACAGTTCTCGACCCCAACGTGTTGGTCACCTGCAATAGGCCAG TGAGCAGGCAGCTGCCTGTAGCACAGTTCTCGGCCCCAACGTGTTGGTCACCTGCAATAGGCCAG A G EFNB1 Ensembl:ENSG00000090776 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:68838722..68838814 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_262841,RMVar_hsa_circ_118533,RMVar_hsa_circ_370977,RMVar_hsa_circ_262842,RMVar_hsa_circ_262840 115445 RMVar_ID_115445 Human_SNP_ID_882688119 m1A Human chrX - 81114956 81114956 81114956 AAAAGAGAAAGAAGATGGAAAAAAAGGTGAAGACGGAAAAGGAAATGGAGAAGATGGAAAAGAGA AAAAGAGAAAGAAGATGGAAAAAAAGGTGAAGGCGGAAAAGGAAATGGAGAAGATGGAAAAGAGA T C HMGN5 Ensembl:ENSG00000198157 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:81114671..81115133 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_95110,Human_RBP_ID_8027571 115446 RMVar_ID_115446 Human_SNP_ID_882696920 m1A Human chrX - 72196889 72196889 72196889 TAATAAGAGCAACATACCCCTTGCCTGGCTTTATCTTCACTATACTGTGCGGCCACTTCATTGAA TAATAAGAGCAACATACCCCTTGCCTGGCTTTGTCTTCACTATACTGTGCGGCCACTTCATTGAA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:72196776..72196925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115447 RMVar_ID_115447 Human_SNP_ID_882704307 m1A Human chrX - 67546514 67546514 67546514 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCACCCCCACCACCACCACACGGTCCATACAA CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCCCCACCACCACCACACGGTCCATACAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:67546441..67546634 26863196 MeRIP-seq:(Medium) rs866187574 Functional Loss SNV ICGC 33..33 33 LICA 1 - 115448 RMVar_ID_115448 Human_SNP_ID_882738804 m1A Human chrX - 136873673 136873673 136873673 GGGTGTCTTCCAACTGAAATCTCAATGTTCTCAGTACGAAAAACCTGAAATCACATGCCTATGTA GGGTGTCTTCCAACTGAAATCTCAATGTTCTCGGTACGAAAAACCTGAAATCACATGCCTATGTA T C RBMX Ensembl:ENSG00000147274 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:136873576..136873700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_729657,Human_RBP_ID_1341270,Human_RBP_ID_1711705,Human_RBP_ID_2071102,Human_RBP_ID_3245022,Human_RBP_ID_9243915,Human_RBP_ID_16831813,Human_RBP_ID_17325239,Human_RBP_ID_22519150,Human_RBP_ID_26772816 Human_miRNA_ID_1796404 RMVar_hsa_circ_264024,RMVar_hsa_circ_286408,RMVar_hsa_circ_367785 115449 RMVar_ID_115449 Human_SNP_ID_882742942 m1A Human chrX + 154411952 154411952 154411952 GCTTGGTGGGCACCTACAGCTGCTTCTGGACCAGTGAGTGGGCCCAGGCCGAGGCAGGCCCGCCC GCTTGGTGGGCACCTACAGCTGCTTCTGGACCGGTGAGTGGGCCCAGGCCGAGGCAGGCCCGCCC A G TAZ Ensembl:ENSG00000102125 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:154411901..154412144 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_Splice_Rec_2248296,Human_Splice_Rec_2248306,Human_Splice_Rec_2248324,Human_Splice_Rec_2248344,Human_Splice_Rec_2248360,Human_Splice_Rec_2248383,Human_Splice_Rec_2248401,Human_Splice_Rec_2248418,Human_Splice_Rec_2248433,Human_Splice_Rec_2248441,Human_Splice_Rec_2248469,Human_Splice_Rec_2248487,Human_Splice_Rec_2248499,Human_Splice_Rec_2248511,Human_Splice_Rec_2248515,Human_Splice_Rec_2248530,Human_Splice_Rec_2248542,Human_Splice_Rec_2248560,Human_Splice_Rec_2248564,Human_Splice_Rec_2248582 115450 RMVar_ID_115450 Human_SNP_ID_882765364 m1A Human chrX - 154349784 154349784 154349784 TGTCGGTGACCATTGACGGCCCCTCCAAGGTGAAGATGGATTGCCAGGAGTGCCCTGAGGGCTAC TGTCGGTGACCATTGACGGCCCCTCCAAGGTGGAGATGGATTGCCAGGAGTGCCCTGAGGGCTAC T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154349661..154349864 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_94416,Human_RBP_ID_848453,Human_RBP_ID_2072093,Human_RBP_ID_8933917,Human_RBP_ID_18197440,Human_RBP_ID_27145769 Human_Splice_Rec_2247412,Human_Splice_Rec_2247502,Human_Splice_Rec_2247685,Human_Splice_Rec_2247776,Human_Splice_Rec_2247860,Human_Splice_Rec_2247902,Human_Splice_Rec_2247912 Human_miRNA_ID_256106,Human_miRNA_ID_830265,Human_miRNA_ID_1196568,Human_miRNA_ID_1374041,Human_miRNA_ID_2709445,Human_miRNA_ID_2709446,Human_miRNA_ID_3063567,Human_miRNA_ID_3063568 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_120414,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_115493,RMVar_hsa_circ_113552,RMVar_hsa_circ_111213,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264309,RMVar_hsa_circ_264310,RMVar_hsa_circ_264308,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_343845,RMVar_hsa_circ_90901,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264314,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_264315 115451 RMVar_ID_115451 Human_SNP_ID_882765554 m1A Human chrX + 119871971 119871971 119871971 TCCGTCATGGGCGTGTGCTTGTTGATTCCAGGACTGGCTACTGCGTACATCCACAGGTTCACTAA TCCGTCATGGGCGTGTGCTTGTTGATTCCAGGTCTGGCTACTGCGTACATCCACAGGTTCACTAA A T NDUFA1 Ensembl:ENSG00000125356 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chrX:119871851..119871975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_94814,Human_RBP_ID_257958,Human_RBP_ID_726669,Human_RBP_ID_1710467,Human_RBP_ID_5050105,Human_RBP_ID_5124657,Human_RBP_ID_5230688,Human_RBP_ID_5330541,Human_RBP_ID_8711988,Human_RBP_ID_9340013,Human_RBP_ID_16803900,Human_RBP_ID_17667323,Human_RBP_ID_22467747,Human_RBP_ID_22777746,Human_RBP_ID_22840632,Human_RBP_ID_23217268,Human_RBP_ID_24325792,Human_RBP_ID_27142871,Human_RBP_ID_27378922 Human_Splice_Rec_2232402 115452 RMVar_ID_115452 Human_SNP_ID_882796973 m1A Human chrX - 154012638 154012638 154012638 CTTGGCAGCTCTGCATCATCGTCGTCAGAGCCACCGCAGATTATCATCAACCCTGCCCGACAGAA CTTGGCAGCTCTGCATCATCGTCGTCAGAGCCGCCGCAGATTATCATCAACCCTGCCCGACAGAA T C IRAK1 Ensembl:ENSG00000184216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154012589..154012685 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_731432,Human_RBP_ID_1712490,Human_RBP_ID_2072018,Human_RBP_ID_3918873,Human_RBP_ID_7986959,Human_RBP_ID_9244853,Human_RBP_ID_16847668,Human_RBP_ID_18147793 Human_Splice_Rec_2246872,Human_Splice_Rec_2246898,Human_Splice_Rec_2246924,Human_Splice_Rec_2246946,Human_Splice_Rec_2246960,Human_Splice_Rec_2246986,Human_Splice_Rec_2247010 Human_miRNA_ID_3070519 RMVar_hsa_circ_92450,RMVar_hsa_circ_89402,RMVar_hsa_circ_113730,RMVar_hsa_circ_121060,RMVar_hsa_circ_116102,RMVar_hsa_circ_111902,RMVar_hsa_circ_264271,RMVar_hsa_circ_264273,RMVar_hsa_circ_264275,RMVar_hsa_circ_79507,RMVar_hsa_circ_264274,RMVar_hsa_circ_264272,RMVar_hsa_circ_264270,RMVar_hsa_circ_264276 115453 RMVar_ID_115453 Human_SNP_ID_882802421 m1A Human chrX - 40735344 40735344 40735344 CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGACCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG CCGCCCGGAGGCGGCGGCGGGGGCAGCGGCGGCCCCCCGTCAGCCCCAGCCCCTCCTCCCCCGGG T G MED14 Ensembl:ENSG00000180182 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:40735252..40735346 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 HNSC 1 - Human_RBP_ID_9317851 115454 RMVar_ID_115454 Human_SNP_ID_882806096 m1A Human chrX - 53562839 53562838 53562839 CAACCTCAGCCAAGCTTCCACCTTGCAGGCCAACCGAGAAGGTGAGAGTGCCGAGGCCAGAAAGG CAACCTCAGCCAAGCTTCCACCTTGCAGGCCA_CCGAGAAGGTGAGAGTGCCGAGGCCAGAAAGG GT G HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:53562826..53562950 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_257161,Human_RBP_ID_8936600,Human_RBP_ID_9409271,Human_RBP_ID_19148443,Human_RBP_ID_23103033,Human_RBP_ID_26362936,Human_RBP_ID_27149494 Human_Splice_Rec_2209143,Human_Splice_Rec_2209144,Human_Splice_Rec_2209305,Human_Splice_Rec_2209306,Human_Splice_Rec_2209469,Human_Splice_Rec_2209470 RMVar_hsa_circ_49196,RMVar_hsa_circ_104556,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_262524,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_262543,RMVar_hsa_circ_17855,RMVar_hsa_circ_31763,RMVar_hsa_circ_95244,RMVar_hsa_circ_262550,RMVar_hsa_circ_292102,RMVar_hsa_circ_44445,RMVar_hsa_circ_262554 115455 RMVar_ID_115455 Human_SNP_ID_882808367 m1A Human chrX - 47185792 47185792 47185792 AGGGGAGGGAGCCCAGGGTCAGGTCACACCTCACCTCCATGTCATTCTTCTCTAGTGCTTCTAGC AGGGGAGGGAGCCCAGGGTCAGGTCACACCTCTCCTCCATGTCATTCTTCTCTAGTGCTTCTAGC T A RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chrX:47185776..47185800;chrX:47185751..47185800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUAD 2 - 115456 RMVar_ID_115456 Human_SNP_ID_882837988 m1A Human chrX + 153869621 153869621 153869621 TTGTGTCACTGGGCTGCACGTTGCTCAGGATCAGGGCGCCACGCTGAATCCGGTACTTCTGGTCT TTGTGTCACTGGGCTGCACGTTGCTCAGGATCGGGGCGCCACGCTGAATCCGGTACTTCTGGTCT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:153869571..153869674 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 115457 RMVar_ID_115457 Human_SNP_ID_882874717 m1A Human chrX + 73827519 73827519 73827519 GGCACGCAGGGGAGGAGAGAGAGAATAGCCCAAGAGAGGCAGAAAGGAAATGCAGAAATGAGAAA GGCACGCAGGGGAGGAGAGAGAGAATAGCCCAGGAGAGGCAGAAAGGAAATGCAGAAATGAGAAA A G TSIX Ensembl:ENSG00000270641 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chrX:73827418..73827796 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 115458 RMVar_ID_115458 Human_SNP_ID_882893319 m1A Human chrX - 48467774 48467774 48467774 CTATTTCCCTGCCCTATCCAGCTACAGGCAAGAACGTGAGGGCTTCCTGCCCAGTCGTGGTCCTG CTATTTCCCTGCCCTATCCAGCTACAGGCAAGCACGTGAGGGCTTCCTGCCCAGTCGTGGTCCTG T G SLC38A5 Ensembl:ENSG00000017483 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:48467701..48467800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_799059,Human_RBP_ID_3976453,Human_RBP_ID_19026602,Human_RBP_ID_26362782 Human_Splice_Rec_2202599,Human_Splice_Rec_2202600,Human_Splice_Rec_2202674,Human_Splice_Rec_2202675,Human_Splice_Rec_2202731,Human_Splice_Rec_2202732,Human_Splice_Rec_2202751,Human_Splice_Rec_2202752,Human_Splice_Rec_2202770,Human_Splice_Rec_2202771,Human_Splice_Rec_2202788,Human_Splice_Rec_2202789,Human_Splice_Rec_2202804,Human_Splice_Rec_2202805,Human_Splice_Rec_2202818,Human_Splice_Rec_2202819 RMVar_hsa_circ_27917,RMVar_hsa_circ_77968,RMVar_hsa_circ_262352 115459 RMVar_ID_115459 Human_SNP_ID_882921742 m1A Human chrX - 129926132 129926132 129926132 GGCGAGGGGAGAACCCGGTGCCCTTTTGACAGACTTTCTTCGGCATTCTTACCGGCGTCTTTTCT GGCGAGGGGAGAACCCGGTGCCCTTTTGACAGCCTTTCTTCGGCATTCTTACCGGCGTCTTTTCT T G AL034405.1 Ensembl:ENSG00000235189 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:129926130..129926218 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_55805 115460 RMVar_ID_115460 Human_SNP_ID_882925305 m1A Human chrX + 119470492 119470492 119470492 ATCCATTTGACACTGTTCGCCGCCGCATGATGATGCAGTCAGGGCGCAAAGGAAGTAAGTTCCAC ATCCATTTGACACTGTTCGCCGCCGCATGATGGTGCAGTCAGGGCGCAAAGGAAGTAAGTTCCAC A G SLC25A5 Ensembl:ENSG00000005022 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:119470371..119470554 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_726408,Human_RBP_ID_3914609,Human_RBP_ID_16800802,Human_RBP_ID_17442777,Human_RBP_ID_17717542,Human_RBP_ID_18144305,Human_RBP_ID_18197625,Human_RBP_ID_24325110,Human_RBP_ID_26835015 Human_Splice_Rec_2232046,Human_Splice_Rec_2232052,Human_Splice_Rec_2232054 115461 RMVar_ID_115461 Human_SNP_ID_882930763 m1A Human chrX + 154400470 154400470 154400470 TCTGACCTTGCACTACCCCAATGTAGGCTCCAAACAGGCATGCGAGGTGCCTTTGGAAAGCCCCA TCTGACCTTGCACTACCCCAATGTAGGCTCCAGACAGGCATGCGAGGTGCCTTTGGAAAGCCCCA A G RPL10 Ensembl:ENSG00000147403 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154400443..154400675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_257498,Human_RBP_ID_799014,Human_RBP_ID_968199,Human_RBP_ID_16849770,Human_RBP_ID_17327942,Human_RBP_ID_17442845,Human_RBP_ID_17556189,Human_RBP_ID_18197518,Human_RBP_ID_22467835,Human_RBP_ID_22631498,Human_RBP_ID_23217082 Human_Splice_Rec_2248051,Human_Splice_Rec_2248067,Human_Splice_Rec_2248077,Human_Splice_Rec_2248089,Human_Splice_Rec_2248099,Human_Splice_Rec_2248129,Human_Splice_Rec_2248141,Human_Splice_Rec_2248149,Human_Splice_Rec_2248161,Human_Splice_Rec_2248165 Human_miRNA_ID_108911,Human_miRNA_ID_1499938,Human_miRNA_ID_1965047,Human_miRNA_ID_2764501 RMVar_hsa_circ_98664,RMVar_hsa_circ_115895,RMVar_hsa_circ_264494,RMVar_hsa_circ_264498,RMVar_hsa_circ_87660,RMVar_hsa_circ_264499,RMVar_hsa_circ_271882 115462 RMVar_ID_115462 Human_SNP_ID_882937613 m1A Human chrX - 71249402 71249402 71249402 AGGGCTGTGGAAGGGGGTGTGGTTCTTGGGTTATAAATAAAGGTGGCTGATGGGTCAAGGGCTGG AGGGCTGTGGAAGGGGGTGTGGTTCTTGGGTTTTAAATAAAGGTGGCTGATGGGTCAAGGGCTGG T A ZMYM3 Ensembl:ENSG00000147130 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:71249351..71249437 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_1063161,Human_RBP_ID_8015351,Human_RBP_ID_24349938 RMVar_hsa_circ_96529,RMVar_hsa_circ_262905,RMVar_hsa_circ_40799,RMVar_hsa_circ_119672,RMVar_hsa_circ_262906 115463 RMVar_ID_115463 Human_SNP_ID_882958570 m1A Human chrX + 117899215 117899215 117899215 CAAGGATAGGTGAATAGTATTCACAGCTTAGGACATCATCATAATCACTTGTTCCTCTGAAGTGA CAAGGATAGGTGAATAGTATTCACAGCTTAGGTCATCATCATAATCACTTGTTCCTCTGAAGTGA A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:117899102..117899335 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - 115464 RMVar_ID_115464 Human_SNP_ID_882961192 m1A Human chrX + 153723274 153723274 153723274 CATCCTGTTGCTAGAAGGTTTCCCACAGGAAGATGTGAGCTTGTTTCCTGGCAGGGCACAAAAGG CATCCTGTTGCTAGAAGGTTTCCCACAGGAAGGTGTGAGCTTGTTTCCTGGCAGGGCACAAAAGG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chrX:153723176..153723300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115465 RMVar_ID_115465 Human_SNP_ID_882990156 m1A Human chrX - 154352867 154352867 154352867 TGAGGGCCCCAGCAAGGTGGACATCAACACAGAGGACCTGGAGGACGGGACGTGCAGGGTCACCT TGAGGGCCCCAGCAAGGTGGACATCAACACAGGGGACCTGGAGGACGGGACGTGCAGGGTCACCT T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chrX:154352754..154352909;chrX:154352751..154352925 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUAD 2 - Human_RBP_ID_94426,Human_RBP_ID_1061635,Human_RBP_ID_2072098,Human_RBP_ID_3247513,Human_RBP_ID_5080325,Human_RBP_ID_5637483,Human_RBP_ID_7987412,Human_RBP_ID_8715432,Human_RBP_ID_8933959,Human_RBP_ID_9265444,Human_RBP_ID_17440796,Human_RBP_ID_27163365,Human_RBP_ID_27550652 Human_Splice_Rec_2247398,Human_Splice_Rec_2247399,Human_Splice_Rec_2247488,Human_Splice_Rec_2247489,Human_Splice_Rec_2247579,Human_Splice_Rec_2247671,Human_Splice_Rec_2247672,Human_Splice_Rec_2247762,Human_Splice_Rec_2247763,Human_Splice_Rec_2247892,Human_Splice_Rec_2247893,Human_Splice_Rec_2247922,Human_Splice_Rec_2247923,Human_Splice_Rec_2247929,Human_Splice_Rec_2247942,Human_Splice_Rec_2247943 Human_miRNA_ID_1967574,Human_miRNA_ID_3045368 RMVar_hsa_circ_89125,RMVar_hsa_circ_103907,RMVar_hsa_circ_109959,RMVar_hsa_circ_113291,RMVar_hsa_circ_116317,RMVar_hsa_circ_120342,RMVar_hsa_circ_117369,RMVar_hsa_circ_114501,RMVar_hsa_circ_113552,RMVar_hsa_circ_111743,RMVar_hsa_circ_109989,RMVar_hsa_circ_105445,RMVar_hsa_circ_106963,RMVar_hsa_circ_104303,RMVar_hsa_circ_97646,RMVar_hsa_circ_99746,RMVar_hsa_circ_101710,RMVar_hsa_circ_99670,RMVar_hsa_circ_92106,RMVar_hsa_circ_97011,RMVar_hsa_circ_90340,RMVar_hsa_circ_264289,RMVar_hsa_circ_264297,RMVar_hsa_circ_264305,RMVar_hsa_circ_75892,RMVar_hsa_circ_79866,RMVar_hsa_circ_86329,RMVar_hsa_circ_75954,RMVar_hsa_circ_264307,RMVar_hsa_circ_264306,RMVar_hsa_circ_264301,RMVar_hsa_circ_264303,RMVar_hsa_circ_264304,RMVar_hsa_circ_264302,RMVar_hsa_circ_264299,RMVar_hsa_circ_264300,RMVar_hsa_circ_264298,RMVar_hsa_circ_264293,RMVar_hsa_circ_264295,RMVar_hsa_circ_264296,RMVar_hsa_circ_264294,RMVar_hsa_circ_264291,RMVar_hsa_circ_264292,RMVar_hsa_circ_264290,RMVar_hsa_circ_127304,RMVar_hsa_circ_264285,RMVar_hsa_circ_264287,RMVar_hsa_circ_264288,RMVar_hsa_circ_264286,RMVar_hsa_circ_264283,RMVar_hsa_circ_264284,RMVar_hsa_circ_85704,RMVar_hsa_circ_264312,RMVar_hsa_circ_121135,RMVar_hsa_circ_125999,RMVar_hsa_circ_95858,RMVar_hsa_circ_264318,RMVar_hsa_circ_78819,RMVar_hsa_circ_79269,RMVar_hsa_circ_264320,RMVar_hsa_circ_264321,RMVar_hsa_circ_264319,RMVar_hsa_circ_264316,RMVar_hsa_circ_264317,RMVar_hsa_circ_110880,RMVar_hsa_circ_122773,RMVar_hsa_circ_77132,RMVar_hsa_circ_76134,RMVar_hsa_circ_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_376174,RMVar_hsa_circ_264325,RMVar_hsa_circ_369392,RMVar_hsa_circ_97350,RMVar_hsa_circ_264326,RMVar_hsa_circ_46907,RMVar_hsa_circ_264328,RMVar_hsa_circ_264329,RMVar_hsa_circ_264327,RMVar_hsa_circ_107538,RMVar_hsa_circ_78188,RMVar_hsa_circ_77997,RMVar_hsa_circ_113822,RMVar_hsa_circ_124307,RMVar_hsa_circ_264332,RMVar_hsa_circ_264333,RMVar_hsa_circ_125720,RMVar_hsa_circ_114261,RMVar_hsa_circ_89680,RMVar_hsa_circ_97390,RMVar_hsa_circ_80213,RMVar_hsa_circ_115724,RMVar_hsa_circ_264336,RMVar_hsa_circ_264338,RMVar_hsa_circ_264340,RMVar_hsa_circ_264341,RMVar_hsa_circ_264339,RMVar_hsa_circ_264337,RMVar_hsa_circ_264334,RMVar_hsa_circ_264335,RMVar_hsa_circ_126694,RMVar_hsa_circ_94395,RMVar_hsa_circ_96792,RMVar_hsa_circ_81623,RMVar_hsa_circ_104448,RMVar_hsa_circ_109978,RMVar_hsa_circ_125060,RMVar_hsa_circ_264342,RMVar_hsa_circ_264344,RMVar_hsa_circ_264346,RMVar_hsa_circ_264347,RMVar_hsa_circ_264345,RMVar_hsa_circ_264343,RMVar_hsa_circ_125573,RMVar_hsa_circ_270064,RMVar_hsa_circ_117980,RMVar_hsa_circ_124437,RMVar_hsa_circ_113860,RMVar_hsa_circ_108965,RMVar_hsa_circ_109911,RMVar_hsa_circ_108067,RMVar_hsa_circ_264353,RMVar_hsa_circ_264361,RMVar_hsa_circ_87965,RMVar_hsa_circ_92898,RMVar_hsa_circ_95730,RMVar_hsa_circ_88211,RMVar_hsa_circ_80396,RMVar_hsa_circ_87183,RMVar_hsa_circ_264363,RMVar_hsa_circ_264365,RMVar_hsa_circ_76130,RMVar_hsa_circ_264364,RMVar_hsa_circ_264362,RMVar_hsa_circ_264357,RMVar_hsa_circ_264359,RMVar_hsa_circ_264360,RMVar_hsa_circ_264358,RMVar_hsa_circ_264355,RMVar_hsa_circ_264356,RMVar_hsa_circ_264354,RMVar_hsa_circ_264349,RMVar_hsa_circ_264351,RMVar_hsa_circ_264352,RMVar_hsa_circ_264350,RMVar_hsa_circ_264348 115466 RMVar_ID_115466 Human_SNP_ID_882997898 m1A Human chrX - 136169844 136169844 136169844 GGCAAAGTTACCTTTTTAGAAGCAAAGTTCTGAATTCTAAAAAAATAAAGTCAACTTCCTATGAA GGCAAAGTTACCTTTTTAGAAGCAAAGTTCTGCATTCTAAAAAAATAAAGTCAACTTCCTATGAA T G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chrX:136169842..136170000 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 115467 RMVar_ID_115467 Human_SNP_ID_883002306 m1A Human chrX + 71129790 71129790 71129790 GCAGTGGTGGTCGGAGGCAGGGTGGCCGCAACATCTCTGTGGAGACAGCCAGTCTGGATGTCTAT GCAGTGGTGGTCGGAGGCAGGGTGGCCGCAACTTCTCTGTGGAGACAGCCAGTCTGGATGTCTAT A T MED12 Ensembl:ENSG00000184634 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:71129739..71129817 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_257607,Human_RBP_ID_966947,Human_RBP_ID_5411827,Human_RBP_ID_9318061,Human_RBP_ID_19026742,Human_RBP_ID_27150399 Human_Splice_Rec_2215319,Human_Splice_Rec_2215405,Human_Splice_Rec_2215489 RMVar_hsa_circ_65981,RMVar_hsa_circ_28860,RMVar_hsa_circ_262890,RMVar_hsa_circ_120769 115468 RMVar_ID_115468 Human_SNP_ID_883026080 m1A Human chrX - 154420735 154420735 154420735 GACAGCTACGGGGGACCCAGGAGGAAACTCACAGCCGACTTGTTCTCCGCCCGGAGCCGCTCGAG GACAGCTACGGGGGACCCAGGAGGAAACTCACTGCCGACTTGTTCTCCGCCCGGAGCCGCTCGAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:154420701..154420750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUAD 2 - 115469 RMVar_ID_115469 Human_SNP_ID_883052128 m1A Human chrX - 154439056 154439056 154439056 CTTGTAGACAAAGCTGCCCTCCACCACCTTGAAGTCCAGGTAGCGAGTCACCTCTGTATACAGTA CTTGTAGACAAAGCTGCCCTCCACCACCTTGACGTCCAGGTAGCGAGTCACCTCTGTATACAGTA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:154438977..154439140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 HNSC 2 - 115470 RMVar_ID_115470 Human_SNP_ID_883063777 m1A Human chrX - 53562190 53562190 53562190 TGAGGATGAGGAGGAGCACACTCAGGAAGAGGACAGCAGTGGCAGTAACGAGGATGAGGATGATA TGAGGATGAGGAGGAGCACACTCAGGAAGAGGGCAGCAGTGGCAGTAACGAGGATGAGGATGATA T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chrX:53562074..53562261;chrX:53562054..53562269 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_5535645,Human_RBP_ID_8936594,Human_RBP_ID_9317983,Human_RBP_ID_18197590,Human_RBP_ID_24550042,Human_RBP_ID_26362935 Human_Splice_Rec_2209145,Human_Splice_Rec_2209146,Human_Splice_Rec_2209307,Human_Splice_Rec_2209308,Human_Splice_Rec_2209471,Human_Splice_Rec_2209472 Human_miRNA_ID_2571603,Human_miRNA_ID_3045338 RMVar_hsa_circ_75758,RMVar_hsa_circ_49196,RMVar_hsa_circ_262512,RMVar_hsa_circ_104556,RMVar_hsa_circ_262513,RMVar_hsa_circ_126578,RMVar_hsa_circ_262524,RMVar_hsa_circ_113187,RMVar_hsa_circ_262530,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_262543,RMVar_hsa_circ_17855,RMVar_hsa_circ_31763,RMVar_hsa_circ_95244,RMVar_hsa_circ_262550,RMVar_hsa_circ_313802,RMVar_hsa_circ_292102,RMVar_hsa_circ_262553,RMVar_hsa_circ_44445,RMVar_hsa_circ_262554 115471 RMVar_ID_115471 Human_SNP_ID_883096089 m1A Human chrX - 53412055 53412054 53412055 CTGTCAGTGGAGAAGGCTCGGCAGGAGTTTGAAGAACGGATGGAAGAAGAGAGTCAGAGTCAGGG CTGTCAGTGGAGAAGGCTCGGCAGGAGTTTGA_GAACGGATGGAAGAAGAGAGTCAGAGTCAGGG CT C SMC1A Ensembl:ENSG00000072501 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:53409101..53413450;chrX:53409030..53413450;chrX:53409126..53413375 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 THCA 1 - Human_RBP_ID_220768,Human_RBP_ID_848135,Human_RBP_ID_3258935,Human_RBP_ID_5067599,Human_RBP_ID_8009107,Human_RBP_ID_8239796,Human_RBP_ID_9317443,Human_RBP_ID_9409238,Human_RBP_ID_16904923,Human_RBP_ID_17554859,Human_RBP_ID_22841696,Human_RBP_ID_23102875,Human_RBP_ID_24549916,Human_RBP_ID_26362911,Human_RBP_ID_27149314,Human_RBP_ID_27833866 Human_Splice_Rec_2208817,Human_Splice_Rec_2208866 RMVar_hsa_circ_350237,RMVar_hsa_circ_71480,RMVar_hsa_circ_66233,RMVar_hsa_circ_59215,RMVar_hsa_circ_354760,RMVar_hsa_circ_72604,RMVar_hsa_circ_32872,RMVar_hsa_circ_358392,RMVar_hsa_circ_262495,RMVar_hsa_circ_285116 115472 RMVar_ID_115472 Human_SNP_ID_883100089 m1A Human chrX + 53405101 53405101 53405101 CTTGAGCCGCATCTGCAGTCCATGGGCCTGAGACTGCACCTGACGCAGCTCTGCCTCTTTCCGTT CTTGAGCCGCATCTGCAGTCCATGGGCCTGAGGCTGCACCTGACGCAGCTCTGCCTCTTTCCGTT A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:53405076..53405100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115473 RMVar_ID_115473 Human_SNP_ID_883126026 m1A Human chrX - 134515368 134515367 134515368 CTCTCTCTTTCTTTTCTTTCTTTCTTTGTCCGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAG CTCTCTCTTTCTTTTCTTTCTTTCTTTGTCCG_GTTTCACTCTTGTTGCCCAGGCTGGAGTGCAG CT C RF00017-4490 RNACentral:URS0000941A94 SRP RNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chrX:134515308..134515401 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 RECA 1 - 115474 RMVar_ID_115474 Human_SNP_ID_883141314 m1A Human chrX + 155071614 155071607 155071614 TTCCTCGTTTGTCTCAACCACGCTCTGAGCACAGAGAAGGAGGAAGTAATGGGGCTGTGCATAGG TTCCTCGTTTGTCTCAACCACGCTCT_______GAGAAGGAGGAAGTAATGGGGCTGTGCATAGG TGAGCACA T BRCC3 Ensembl:ENSG00000185515 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:155071504..155071633 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 27..33 33 LAML 1 - Human_RBP_ID_732096,Human_RBP_ID_5058754 Human_Splice_Rec_2250312,Human_Splice_Rec_2250348,Human_Splice_Rec_2250364,Human_Splice_Rec_2250395,Human_Splice_Rec_2250405 RMVar_hsa_circ_51822 115475 RMVar_ID_115475 Human_SNP_ID_883174606 m1A Human chrX - 154019445 154019445 154019445 CCTCACGCACCTGCAGCTGCTCCGTGCGCGGGACATCATCACAGCCTGTGAGCGCGGGACTCCGG CCTCACGCACCTGCAGCTGCTCCGTGCGCGGGGCATCATCACAGCCTGTGAGCGCGGGACTCCGG T C IRAK1 Ensembl:ENSG00000184216 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:154019206..154019900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_731468,Human_RBP_ID_1061591,Human_RBP_ID_5080247,Human_RBP_ID_5155539,Human_RBP_ID_17443003,Human_RBP_ID_18197434,Human_RBP_ID_27145656 Human_Splice_Rec_2246853,Human_Splice_Rec_2246877,Human_Splice_Rec_2246903,Human_Splice_Rec_2246927,Human_Splice_Rec_2246965,Human_Splice_Rec_2246989 RMVar_hsa_circ_89402,RMVar_hsa_circ_111902,RMVar_hsa_circ_264271,RMVar_hsa_circ_264270,RMVar_hsa_circ_77807,RMVar_hsa_circ_102469,RMVar_hsa_circ_112885,RMVar_hsa_circ_264280,RMVar_hsa_circ_264281,RMVar_hsa_circ_264282 115476 RMVar_ID_115476 Human_SNP_ID_883175719 m1A Human chrX + 51332989 51332989 51332989 GCCTCGAGGATGAAGTGCAAACCCAACCAGACACGGACCTACGACCCCGAGGGGTTCAAGAAGCG GCCTCGAGGATGAAGTGCAAACCCAACCAGACGCGGACCTACGACCCCGAGGGGTTCAAGAAGCG A G NUDT10 Ensembl:ENSG00000122824 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs2625875 Functional Loss SNV ICGC 33..33 33 LICA 3 - 115477 RMVar_ID_115477 Human_SNP_ID_883191784 m1A Human chrX - 154532456 154532456 154532456 TCAGCAAGACACTCTCTCCCTCACAGAACGTGAAGCTCCCTGACGCCTATGAGCGCCTCATCCTG TCAGCAAGACACTCTCTCCCTCACAGAACGTGGAGCTCCCTGACGCCTATGAGCGCCTCATCCTG T C G6PD Ensembl:ENSG00000160211 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154532426..154532475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_731967,Human_RBP_ID_9340112 Human_Splice_Rec_2249430,Human_Splice_Rec_2249431,Human_Splice_Rec_2249454,Human_Splice_Rec_2249455,Human_Splice_Rec_2249478,Human_Splice_Rec_2249479,Human_Splice_Rec_2249484,Human_Splice_Rec_2249485 RMVar_hsa_circ_37596,RMVar_hsa_circ_97331,RMVar_hsa_circ_125049,RMVar_hsa_circ_128070,RMVar_hsa_circ_109568,RMVar_hsa_circ_114290,RMVar_hsa_circ_102166,RMVar_hsa_circ_109243,RMVar_hsa_circ_264556,RMVar_hsa_circ_264560,RMVar_hsa_circ_80187,RMVar_hsa_circ_78607,RMVar_hsa_circ_264558,RMVar_hsa_circ_264559,RMVar_hsa_circ_264557,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553,RMVar_hsa_circ_100622,RMVar_hsa_circ_103239,RMVar_hsa_circ_93275,RMVar_hsa_circ_94632,RMVar_hsa_circ_264563,RMVar_hsa_circ_264564,RMVar_hsa_circ_264565,RMVar_hsa_circ_378627,RMVar_hsa_circ_264562,RMVar_hsa_circ_344692,RMVar_hsa_circ_264567,RMVar_hsa_circ_84762,RMVar_hsa_circ_264566 115478 RMVar_ID_115478 Human_SNP_ID_883191786 m1A Human chrX - 154532456 154532456 154532456 TCAGCAAGACACTCTCTCCCTCACAGAACGTGAAGCTCCCTGACGCCTATGAGCGCCTCATCCTG TCAGCAAGACACTCTCTCCCTCACAGAACGTGCAGCTCCCTGACGCCTATGAGCGCCTCATCCTG T G G6PD Ensembl:ENSG00000160211 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:154532426..154532475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - Human_RBP_ID_731967,Human_RBP_ID_9340112 Human_Splice_Rec_2249430,Human_Splice_Rec_2249431,Human_Splice_Rec_2249454,Human_Splice_Rec_2249455,Human_Splice_Rec_2249478,Human_Splice_Rec_2249479,Human_Splice_Rec_2249484,Human_Splice_Rec_2249485 RMVar_hsa_circ_37596,RMVar_hsa_circ_97331,RMVar_hsa_circ_125049,RMVar_hsa_circ_128070,RMVar_hsa_circ_109568,RMVar_hsa_circ_114290,RMVar_hsa_circ_102166,RMVar_hsa_circ_109243,RMVar_hsa_circ_264556,RMVar_hsa_circ_264560,RMVar_hsa_circ_80187,RMVar_hsa_circ_78607,RMVar_hsa_circ_264558,RMVar_hsa_circ_264559,RMVar_hsa_circ_264557,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553,RMVar_hsa_circ_100622,RMVar_hsa_circ_103239,RMVar_hsa_circ_93275,RMVar_hsa_circ_94632,RMVar_hsa_circ_264563,RMVar_hsa_circ_264564,RMVar_hsa_circ_264565,RMVar_hsa_circ_378627,RMVar_hsa_circ_264562,RMVar_hsa_circ_344692,RMVar_hsa_circ_264567,RMVar_hsa_circ_84762,RMVar_hsa_circ_264566 115479 RMVar_ID_115479 Human_SNP_ID_883200087 m1A Human chrX - 154398396 154398396 154398396 GGCACCGCAAGAGACGACAACTGCGCTTACTCACCACACCGAAGGGAAAGAGGCGCTCCTCCGCC GGCACCGCAAGAGACGACAACTGCGCTTACTCGCCACACCGAAGGGAAAGAGGCGCTCCTCCGCC T C AC245140.2 Ensembl:ENSG00000280195 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chrX:154398351..154398550 26863196 MeRIP-seq:(Medium) rs1557184854 Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - 115480 RMVar_ID_115480 Human_SNP_ID_883227362 m1A Human chrX + 49117039 49117039 49117039 AGCTCTACAAGAGGCTCACTCACTGAGATCCAAGGTGTTCTTGTCAAACTCCTGCTGGGAGACAG AGCTCTACAAGAGGCTCACTCACTGAGATCCACGGTGTTCTTGTCAAACTCCTGCTGGGAGACAG A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:49115926..49123675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115481 RMVar_ID_115481 Human_SNP_ID_883251622 m1A Human chrX + 53625853 53625853 53625853 CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCAGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG CCGGGACCAGGACCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCGGGGCCAGG A G RF00017-1020,RF00017-4520 RNACentral:URS000099BA6B,RNACentral:URS000099C2D3 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chrX:53625851..53625875 26863196 MeRIP-seq:(Medium) rs185693518 Functional Loss SNV ICGC 33..33 33 COCA 1 - 115482 RMVar_ID_115482 Human_SNP_ID_883266102 m1A Human chrX + 53433879 53433879 53433879 CCAGGCCCGAGGCTCCTCCGGTTATTACCGCCACCAGGCCCTGTCAAAAGGGACATGGTCAGGGT CCAGGCCCGAGGCTCCTCCGGTTATTACCGCCGCCAGGCCCTGTCAAAAGGGACATGGTCAGGGT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chrX:53433671..53433914;chrX:53433701..53433924;chrX:53433690..53433918;chrX:53433701..53434179;chrX:53433666..53433906 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - 115483 RMVar_ID_115483 Human_SNP_ID_883267155 m1A Human chrX - 65733282 65733282 65733282 GTACCTGTCTTGGTCAGAGGGAGGAATCACTCACCGGGGCTTTTTTGTCAATGGGCTTGATGACA GTACCTGTCTTGGTCAGAGGGAGGAATCACTCGCCGGGGCTTTTTTGTCAATGGGCTTGATGACA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chrX:65733276..65733300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115484 RMVar_ID_115484 Human_SNP_ID_883311565 m1A Human chrX + 53562919 53562919 53562919 ATCAGCACGTCCTCTTGTGATTCATCCTCTCCACTTCTGCTCACTGAAGGTTACAGAGCAGAGCC ATCAGCACGTCCTCTTGTGATTCATCCTCTCCGCTTCTGCTCACTGAAGGTTACAGAGCAGAGCC A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chrX:53562826..53562950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - 115485 RMVar_ID_115485 Human_SNP_ID_883318209 m1A Human chrX + 153957418 153957418 153957418 TGGTACTGGGGGAGACGCTGCTGATGCCCAGGATGGTGGGCTTGGTCCCCGCCCCACTGGCCTGC TGGTACTGGGGGAGACGCTGCTGATGCCCAGGGTGGTGGGCTTGGTCCCCGCCCCACTGGCCTGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chrX:153957368..153957474 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115486 RMVar_ID_115486 Human_SNP_ID_883328335 m1A Human chrX + 361532 361531 361532 CGGAGTCCTGCGGGCGTCCTCTGGGGAAGTAGAAGGTCGGAATGCTTTGGCTCGTGGCCGGGGGC CGGAGTCCTGCGGGCGTCCTCTGGGGAAGTAG_AGGTCGGAATGCTTTGGCTCGTGGCCGGGGGC GA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chrX:361481..361634 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 115487 RMVar_ID_115487 Human_SNP_ID_883340654 m1A Human chrX - 53196023 53196000 53196023 GGCAGAAGCATCCACCAGCCACACTTGAGGCCATAATCCGTGAAGCGGAAAACATCCCTGTTCAC GGCAGAAGCATCCACCAGCCACACTTGAGGCC_______________________CCCTGTTCAC GATGTTTTCCGCTTCACGGATTAT G KDM5C Ensembl:ENSG00000126012 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chrX:53196001..53196025 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..55 33 STAD 1 - Human_Splice_Rec_2208374,Human_Splice_Rec_2208421,Human_Splice_Rec_2208466,Human_Splice_Rec_2208515,Human_Splice_Rec_2208563 RMVar_hsa_circ_49092,RMVar_hsa_circ_119424,RMVar_hsa_circ_115048,RMVar_hsa_circ_262471,RMVar_hsa_circ_262472,RMVar_hsa_circ_97513,RMVar_hsa_circ_262473 115488 RMVar_ID_115488 Human_SNP_ID_806327752 m1A Human chr10 - 101060600 101060599 101060600 AACTGTCAGAGAGCTGCCGGAGACCCTGAAAAAGGCCAGAGACGGGGACTTGTGGGGCTGACGAA AACTGTCAGAGAGCTGCCGGAGACCCTGAAAA_GGCCAGAGACGGGGACTTGTGGGGCTGACGAA CT C AL133215.2 Ensembl:ENSG00000273162 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:101060565..101060702 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_4102428,Human_RBP_ID_5547751,Human_RBP_ID_18416169 115489 RMVar_ID_115489 Human_SNP_ID_806336034 m1A Human chr10 - 104315879 104315879 104315879 GCTGCAGCTGGAGCAGTTGCGCCTGGAGGAGGAGGTGGCTCGGCTGGCGGCCGAAAAGGAGGCAC GCTGCAGCTGGAGCAGTTGCGCCTGGAGGAGGTGGTGGCTCGGCTGGCGGCCGAAAAGGAGGCAC T A ITPRIP Ensembl:ENSG00000148841 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:104315776..104315970 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5137930,Human_RBP_ID_22029549 RMVar_hsa_circ_104371,RMVar_hsa_circ_146258,RMVar_hsa_circ_93051,RMVar_hsa_circ_146257 115490 RMVar_ID_115490 Human_SNP_ID_806340408 m1A Human chr10 - 113143951 113143951 113143951 GTGCCAGGCGATAGTGGGTAATACGGGGATATATCTGGAGGGTGCGGAGGCCGTGGGATTCCTGA GTGCCAGGCGATAGTGGGTAATACGGGGATATGTCTGGAGGGTGCGGAGGCCGTGGGATTCCTGA T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:113141213..113144020 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 15 uterus 115491 RMVar_ID_115491 Human_SNP_ID_806364027 m1A Human chr10 + 38526796 38526796 38526796 GGAATGCAATGCAATGGAATGGACTCGAATGGAATGGAATGGAATTGACTCGAATGAAATTGAAT GGAATGCAATGCAATGGAATGGACTCGAATGGCATGGAATGGAATTGACTCGAATGAAATTGAAT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:38526793..38526898 26863196 MeRIP-seq:(Medium) rs1331606354 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115492 RMVar_ID_115492 Human_SNP_ID_806391217 m1A Human chr10 - 17229378 17229378 17229378 TGGCGATGGCCTGGGCGGCGGCGGTGGCGCGGACTGGCTCCCGGAGAAGAGGCGAACGAGGGCGC TGGCGATGGCCTGGGCGGCGGCGGTGGCGCGGCCTGGCTCCCGGAGAAGAGGCGAACGAGGGCGC T G VIM-AS1 Ensembl:ENSG00000229124 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:17229251..17229725 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_5548176,Human_RBP_ID_18431560 Human_Splice_Rec_1115879,Human_Splice_Rec_1115881 RMVar_hsa_circ_142430 115493 RMVar_ID_115493 Human_SNP_ID_806423950 m1A Human chr10 + 68946558 68946558 68946558 CAGAGTCGACAAGGAAGTCGCTCAGGAAGTCGACAAGATGGTAGAAGACGAAGTGGGAATAGAAA CAGAGTCGACAAGGAAGTCGCTCAGGAAGTCGGCAAGATGGTAGAAGACGAAGTGGGAATAGAAA A G DDX50 Ensembl:ENSG00000107625 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:68946447..68946700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_1769536 RMVar_hsa_circ_92087,RMVar_hsa_circ_89745,RMVar_hsa_circ_143933,RMVar_hsa_circ_143934,RMVar_hsa_circ_143935 115494 RMVar_ID_115494 Human_SNP_ID_806427179 m1A Human chr10 - 124610354 124610354 124610354 CCCTCACCCGCTCCACCAGCACCCTCACCCGCACCCTCACCCGCTCCATCAGCACCCTCACCCGC CCCTCACCCGCTCCACCAGCACCCTCACCCGCTCCCTCACCCGCTCCATCAGCACCCTCACCCGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124610350..124610420 26863196 MeRIP-seq:(Medium) rs201250786 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115495 RMVar_ID_115495 Human_SNP_ID_806444403 m1A Human chr10 + 17235274 17235274 17235274 CTATTGGCCGCCTGCAGGATGAGATTCAGAATATGAAGGAGGAAATGGCTCGTCACCTTCGTGAA CTATTGGCCGCCTGCAGGATGAGATTCAGAATGTGAAGGAGGAAATGGCTCGTCACCTTCGTGAA A G VIM Ensembl:ENSG00000026025 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:17235224..17235329 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_375106,Human_RBP_ID_746972,Human_RBP_ID_1444907,Human_RBP_ID_1763836,Human_RBP_ID_3345385,Human_RBP_ID_4140753,Human_RBP_ID_8759933,Human_RBP_ID_9320815,Human_RBP_ID_11323393,Human_RBP_ID_18188024,Human_RBP_ID_22377303,Human_RBP_ID_22787980,Human_RBP_ID_23206595,Human_RBP_ID_23304254,Human_RBP_ID_23447729,Human_RBP_ID_26877818,Human_RBP_ID_27405168 Human_miRNA_ID_546805,Human_miRNA_ID_2195342 RMVar_hsa_circ_10661,RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_112400,RMVar_hsa_circ_40197,RMVar_hsa_circ_82020,RMVar_hsa_circ_142434,RMVar_hsa_circ_142435,RMVar_hsa_circ_117850,RMVar_hsa_circ_37563,RMVar_hsa_circ_78427,RMVar_hsa_circ_95432,RMVar_hsa_circ_119637,RMVar_hsa_circ_142436,RMVar_hsa_circ_142437,RMVar_hsa_circ_103579,RMVar_hsa_circ_142438,RMVar_hsa_circ_142440,RMVar_hsa_circ_142439,RMVar_hsa_circ_75842,RMVar_hsa_circ_92840,RMVar_hsa_circ_142443,RMVar_hsa_circ_23969,RMVar_hsa_circ_333817,RMVar_hsa_circ_87714,RMVar_hsa_circ_142445,RMVar_hsa_circ_142446,RMVar_hsa_circ_142444 115496 RMVar_ID_115496 Human_SNP_ID_806467872 m1A Human chr10 + 97401253 97401253 97401253 GAGCGACCCATGTTGACTAAGCCGTGGCGAGGAATGAGCTTAAATGACCGGCTTCCAGGGACGTA GAGCGACCCATGTTGACTAAGCCGTGGCGAGGGATGAGCTTAAATGACCGGCTTCCAGGGACGTA A G AL355490.3 Ensembl:ENSG00000231970 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:97401203..97401354 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 115497 RMVar_ID_115497 Human_SNP_ID_806505465 m1A Human chr10 + 113729328 113729328 113729328 TCTTTCCTGTTGAAGGCTATTACTCGTGGAGGAGCCCAGGAAGAGGCTCCTGGTTTGTGCAAGCC TCTTTCCTGTTGAAGGCTATTACTCGTGGAGGCGCCCAGGAAGAGGCTCCTGGTTTGTGCAAGCC A C CASP7 Ensembl:ENSG00000165806 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:113729316..113729466 32194978 MeRIP-seq:(Medium) rs200326742 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 9 lung Human_Splice_Rec_1177650,Human_Splice_Rec_1177674,Human_Splice_Rec_1177688,Human_Splice_Rec_1177702,Human_Splice_Rec_1177714,Human_Splice_Rec_1177726,Human_Splice_Rec_1177740,Human_Splice_Rec_1177752,Human_Splice_Rec_1177762,Human_Splice_Rec_1177772,Human_Splice_Rec_1177784 RMVar_hsa_circ_146438 115498 RMVar_ID_115498 Human_SNP_ID_806525173 m1A Human chr10 + 131916787 131916787 131916787 GGGTGGAATGACACAGTGTAGGGACCTCACGCAGGTGGAATGACACAGTGTTTGTAGGGACCTCA GGGTGGAATGACACAGTGTAGGGACCTCACGCGGGTGGAATGACACAGTGTTTGTAGGGACCTCA A G PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:131916779..131916929 26863196 MeRIP-seq:(Medium) rs376559718 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115499 RMVar_ID_115499 Human_SNP_ID_806533709 m1A Human chr10 + 101007411 101007411 101007411 TCACTGTTACCCAGAGGCTCTTGTTACTACCCACTTCATTCCCCACCGCTGCCAGTGCCACTGCC TCACTGTTACCCAGAGGCTCTTGTTACTACCCGCTTCATTCCCCACCGCTGCCAGTGCCACTGCC A G LZTS2 Ensembl:ENSG00000107816 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:101007361..101007486 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_17225172,Human_RBP_ID_17341958,Human_RBP_ID_17457349,Human_RBP_ID_17679262 115500 RMVar_ID_115500 Human_SNP_ID_806541444 m1A Human chr10 - 114526803 114526803 114526803 CGAGCTTCGGAGAGAAGCCTGATATGTAACCCAGGCAGGTGGGAGCCTCAGTCTGTCGGGCTGAG CGAGCTTCGGAGAGAAGCCTGATATGTAACCCGGGCAGGTGGGAGCCTCAGTCTGTCGGGCTGAG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:114526752..114526859 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 9 oesophagus Human_RBP_ID_4107931 RMVar_hsa_circ_11524,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_53410,RMVar_hsa_circ_40012,RMVar_hsa_circ_13353 115501 RMVar_ID_115501 Human_SNP_ID_806545966 m1A Human chr10 - 35667509 35667509 35667509 TGGTAGTGGTGATGGTGGTGATGATGGTGGTGATGGTGGTGATGGTGGTGGTGGTGATGATGGTG TGGTAGTGGTGATGGTGGTGATGATGGTGGTGGTGGTGGTGATGGTGGTGGTGGTGATGATGGTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:35667434..35667557 26863196 MeRIP-seq:(Medium) rs1180772488 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115502 RMVar_ID_115502 Human_SNP_ID_806584688 m1A Human chr10 - 3113071 3113071 3113071 GTCGTTGGACCGGAGTCGAGAATACCGGACACAACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA GTCGTTGGACCGGAGTCGAGAATACCGGACACGACTCAGGGCTCATGTGGAGAAAAGGTGGCTTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3113068..3113235 26863196 MeRIP-seq:(Medium) rs7906901 Functional Loss SNV ICGC 33..33 33 COCA 5 - 115503 RMVar_ID_115503 Human_SNP_ID_806597942 m1A Human chr10 - 16817011 16817011 16817011 GGAGAAGAACCAGCCCGAGGTGGACATGAGTGACCGGGGCATCTCCAACATGCTGGATGTCAACG GGAGAAGAACCAGCCCGAGGTGGACATGAGTGTCCGGGGCATCTCCAACATGCTGGATGTCAACG T A RSU1 Ensembl:ENSG00000148484 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:16727154..16817079 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_22787965 Human_Splice_Rec_1115495,Human_Splice_Rec_1115510,Human_Splice_Rec_1115511 115504 RMVar_ID_115504 Human_SNP_ID_806606488 m1A Human chr10 - 42802161 42802161 42802161 ATCTTTATCATCTTCCCACTTTCCAGTCACGAAGCAATCTCTGATACTGTTCATAACCTTACGCA ATCTTTATCATCTTCCCACTTTCCAGTCACGAGGCAATCTCTGATACTGTTCATAACCTTACGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:42798601..42802212 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 115505 RMVar_ID_115505 Human_SNP_ID_806654940 m1A Human chr10 + 71821990 71821990 71821990 TCTTTCACCTCATCACAGAACCCAACCAGCGCACAGATCTCCTTGGGTTGCTGAAGAGAGCACAG TCTTTCACCTCATCACAGAACCCAACCAGCGCGCAGATCTCCTTGGGTTGCTGAAGAGAGCACAG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:71821940..71822062 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115506 RMVar_ID_115506 Human_SNP_ID_806694261 m1A Human chr10 - 103602615 103602615 103602615 GGAGATCAGCTTCCCCGCGGGCGTGGAGGTGCAGGTGCTGGAGAAGCAGGAGAGCGGGTGGTGGT GGAGATCAGCTTCCCCGCGGGCGTGGAGGTGCGGGTGCTGGAGAAGCAGGAGAGCGGGTGGTGGT T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:103602565..103602776 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_4136039,Human_RBP_ID_5520300,Human_RBP_ID_23431907,Human_RBP_ID_27189606 Human_miRNA_ID_968934,Human_miRNA_ID_1538746,Human_miRNA_ID_1592978 115507 RMVar_ID_115507 Human_SNP_ID_806740448 m1A Human chr10 + 59906346 59906346 59906346 GCCGCCACCGCCGCCGCCCGAGGTCGACGAGCAGGACGACTGCATGGCGGCCGAGCTGCTGCTGT GCCGCCACCGCCGCCGCCCGAGGTCGACGAGCGGGACGACTGCATGGCGGCCGAGCTGCTGCTGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:59906250..59906425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 115508 RMVar_ID_115508 Human_SNP_ID_806744526 m1A Human chr10 + 103396454 103396454 103396454 AAATTCCGCAGCTGGTGTCCTTCAACGAATGTAACCACCTCTCGGCCCGGCCGGAAGAAGCCACC AAATTCCGCAGCTGGTGTCCTTCAACGAATGTTACCACCTCTCGGCCCGGCCGGAAGAAGCCACC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:103396451..103396475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115509 RMVar_ID_115509 Human_SNP_ID_806746253 m1A Human chr10 + 112951604 112951604 112951604 CTCCCCAACGGATCGCTCTCGCCCACCGCCCGAACCGTAAGTGCCTCCGCGCCCGGCCCCCGCCC CTCCCCAACGGATCGCTCTCGCCCACCGCCCGGACCGTAAGTGCCTCCGCGCCCGGCCCCCGCCC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:112951501..112951688 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 13 large intestine Human_Splice_Rec_1176797,Human_Splice_Rec_1176823,Human_Splice_Rec_1176843,Human_Splice_Rec_1176869,Human_Splice_Rec_1176893,Human_Splice_Rec_1176921,Human_Splice_Rec_1176949,Human_Splice_Rec_1176975,Human_Splice_Rec_1177001,Human_Splice_Rec_1177025,Human_Splice_Rec_1177053,Human_Splice_Rec_1177081,Human_Splice_Rec_1177109,Human_Splice_Rec_1177133 RMVar_hsa_circ_55138,RMVar_hsa_circ_51712 115510 RMVar_ID_115510 Human_SNP_ID_806748736 m1A Human chr10 + 7965633 7965633 7965633 GGAGAAAGAAAAGAAAAAGGACAAAAAGGAGAAGAAGAAAAAGAAGGAAAAAGAGAAGGAGAAGA GGAGAAAGAAAAGAAAAAGGACAAAAAGGAGACGAAGAAAAAGAAGGAAAAAGAGAAGGAGAAGA A C TAF3 Ensembl:ENSG00000165632 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:7965072..8009270 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_24541933 RMVar_hsa_circ_266081,RMVar_hsa_circ_360576 115511 RMVar_ID_115511 Human_SNP_ID_806800874 m1A Human chr10 - 18573416 18573416 18573416 GGAATGGAGAATGGAATGGAAAGGAAAATGGAACCGATGGAATGGAAGGGAGAATGGAATGGAAT GGAATGGAGAATGGAATGGAAAGGAAAATGGATCCGATGGAATGGAAGGGAGAATGGAATGGAAT T A NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18573365..18573481 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_191801 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 115512 RMVar_ID_115512 Human_SNP_ID_806825149 m1A Human chr10 - 56359855 56359855 56359855 CACTCATGTACTCATTCCTGGTGGCTCATCTCAGGACAGAAGGCAATTGCAGCTAAGGAACAATG CACTCATGTACTCATTCCTGGTGGCTCATCTCTGGACAGAAGGCAATTGCAGCTAAGGAACAATG T A ZWINT Ensembl:ENSG00000122952 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:56359750..56359885 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_1447519,Human_RBP_ID_5339166,Human_RBP_ID_8335613,Human_RBP_ID_9360348,Human_RBP_ID_11376468,Human_RBP_ID_18431797,Human_RBP_ID_18595183,Human_RBP_ID_19452751,Human_RBP_ID_22536605,Human_RBP_ID_22639336,Human_RBP_ID_22735789,Human_RBP_ID_22882538,Human_RBP_ID_24816859,Human_RBP_ID_26316295 RMVar_hsa_circ_86937,RMVar_hsa_circ_143482 115513 RMVar_ID_115513 Human_SNP_ID_806847908 m1A Human chr10 - 103602462 103602462 103602462 GCTGGACACAGTGCCCGCCAAGGGCAGGCAGAACGAAGGCAAATCAGACAGCCTGGAGAAGATCG GCTGGACACAGTGCCCGCCAAGGGCAGGCAGAGCGAAGGCAAATCAGACAGCCTGGAGAAGATCG T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103602412..103602816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_miRNA_ID_1538745,Human_miRNA_ID_1592977 115514 RMVar_ID_115514 Human_SNP_ID_806855719 m1A Human chr10 + 1675528 1675528 1675528 GGAGGTTTGGGTTTGGGGATGCGTGGATGTTCAGGAGGTTTGGGTTTGGGGGTACATGGATGTTC GGAGGTTTGGGTTTGGGGATGCGTGGATGTTCTGGAGGTTTGGGTTTGGGGGTACATGGATGTTC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:1675350..1675683 26863196 MeRIP-seq:(Medium) rs77814469 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,oesophagus adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 oesophagus,haematopoietic and lymphoid tissue 115515 RMVar_ID_115515 Human_SNP_ID_806906015 m1A Human chr10 + 113165873 113165873 113165873 CCAGCCGCTTTGCAGCCTGCCGCCCCCTCCTCATCAATTGCACAGCCGTCGACTTCTTCCTTACA CCAGCCGCTTTGCAGCCTGCCGCCCCCTCCTCGTCAATTGCACAGCCGTCGACTTCTTCCTTACA A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:113165681..113165983 26863196 MeRIP-seq:(Medium) rs1308135107 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 13 large intestine Human_RBP_ID_17225521,Human_RBP_ID_17457791,Human_RBP_ID_18931920,Human_RBP_ID_22420424 Human_Splice_Rec_1177260 115516 RMVar_ID_115516 Human_SNP_ID_806908585 m1A Human chr10 - 18567799 18567799 18567799 GAATGTAAAGGAATGGAATGGAGAATGGAATGAAGAATGTAGAATGCAATGGAATGGAGAATGGA GAATGTAAAGGAATGGAATGGAGAATGGAATGGAGAATGTAGAATGCAATGGAATGGAGAATGGA T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:18567751..18567834 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_8331527,Human_RBP_ID_23448228 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 115517 RMVar_ID_115517 Human_SNP_ID_806953113 m1A Human chr10 + 5765970 5765970 5765970 GATTTCATTATATGCATTATTTGCCAAATTTTAAATGTGTCCTAATTACATAATAACATGTACTG GATTTCATTATATGCATTATTTGCCAAATTTTGAATGTGTCCTAATTACATAATAACATGTACTG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:5765919..5766069 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_2221033 115518 RMVar_ID_115518 Human_SNP_ID_806955150 m1A Human chr10 + 23095721 23095721 23095721 CGGCGGGCCCGGCACCGGGCCGGGACTGGGGGAGGCAGGTAGGACGCGGGTCCCGCAGGCCCCGC CGGCGGGCCCGGCACCGGGCCGGGACTGGGGGGGGCAGGTAGGACGCGGGTCCCGCAGGCCCCGC A G MSRB2 Ensembl:ENSG00000148450 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr10:23095652..23104167 26863410 MeRIP-seq:(Medium) rs911851386 Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_4136192,Human_RBP_ID_9320514 Human_Splice_Rec_1118579 115519 RMVar_ID_115519 Human_SNP_ID_806978653 m1A Human chr10 + 49964657 49964657 49964657 AAAAAATGAAATAAATGAAATGATGAAATGAAATAATGAAATGAATAATGAAATGCCAGGTGCAG AAAAAATGAAATAAATGAAATGATGAAATGAAGTAATGAAATGAATAATGAAATGCCAGGTGCAG A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:49964600..49964695 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_9443872 RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 115520 RMVar_ID_115520 Human_SNP_ID_806991172 m1A Human chr10 - 102157525 102157525 102157525 ACCTGGACAGGCTGTTTCTTTTGGTCCTCCTCATCATCATCATCACTGGACTCTTCACTGCTGCT ACCTGGACAGGCTGTTTCTTTTGGTCCTCCTCCTCATCATCATCACTGGACTCTTCACTGCTGCT T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:102157476..102157525 26863196 MeRIP-seq:(Medium) rs139625185 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,COCA,LIHC,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 12 liver,large intestine GWAS_ID_9594 115521 RMVar_ID_115521 Human_SNP_ID_807013436 m1A Human chr10 + 41859937 41859937 41859937 GGAATGGAATGGAATGGAATGGAATCAACCCGAGTGCAATGGAATGGAATGGAATGGAATGGAAT GGAATGGAATGGAATGGAATGGAATCAACCCGTGTGCAATGGAATGGAATGGAATGGAATGGAAT A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41859887..41860170 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 115522 RMVar_ID_115522 Human_SNP_ID_807074219 m1A Human chr10 + 126970754 126970754 126970754 AGAGGAGCGGATGAACTTTCTTTACAGATCGGAGACACTGTGCACATCTTAGAAACATATGAAGG AGAGGAGCGGATGAACTTTCTTTACAGATCGGTGACACTGTGCACATCTTAGAAACATATGAAGG A T DOCK1 Ensembl:ENSG00000150760 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:126970701..126970800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_1762849,Human_RBP_ID_5459791,Human_RBP_ID_5520376,Human_RBP_ID_5545251,Human_RBP_ID_11307366,Human_RBP_ID_22879171 Human_Splice_Rec_1187952,Human_Splice_Rec_1187953,Human_Splice_Rec_1188054,Human_Splice_Rec_1188055 Human_miRNA_ID_1995752,Human_miRNA_ID_2228248,Human_miRNA_ID_2504229 RMVar_hsa_circ_108908,RMVar_hsa_circ_293903,RMVar_hsa_circ_309985,RMVar_hsa_circ_327181,RMVar_hsa_circ_356447,RMVar_hsa_circ_375674,RMVar_hsa_circ_371693,RMVar_hsa_circ_350151,RMVar_hsa_circ_355933,RMVar_hsa_circ_335420,RMVar_hsa_circ_315886,RMVar_hsa_circ_317184,RMVar_hsa_circ_312465,RMVar_hsa_circ_303839,RMVar_hsa_circ_306859,RMVar_hsa_circ_303757,RMVar_hsa_circ_126800,RMVar_hsa_circ_282617,RMVar_hsa_circ_289042,RMVar_hsa_circ_292150,RMVar_hsa_circ_284647,RMVar_hsa_circ_280980,RMVar_hsa_circ_282287,RMVar_hsa_circ_273184,RMVar_hsa_circ_119815,RMVar_hsa_circ_122897,RMVar_hsa_circ_122922,RMVar_hsa_circ_119950,RMVar_hsa_circ_118430,RMVar_hsa_circ_119036,RMVar_hsa_circ_116315,RMVar_hsa_circ_57852,RMVar_hsa_circ_83722,RMVar_hsa_circ_91893,RMVar_hsa_circ_99913,RMVar_hsa_circ_104029,RMVar_hsa_circ_92981,RMVar_hsa_circ_86451,RMVar_hsa_circ_88856,RMVar_hsa_circ_85382,RMVar_hsa_circ_75989,RMVar_hsa_circ_78072,RMVar_hsa_circ_81059,RMVar_hsa_circ_77938,RMVar_hsa_circ_66778,RMVar_hsa_circ_75684,RMVar_hsa_circ_60900,RMVar_hsa_circ_147072,RMVar_hsa_circ_147080,RMVar_hsa_circ_147088,RMVar_hsa_circ_147092,RMVar_hsa_circ_147096,RMVar_hsa_circ_147098,RMVar_hsa_circ_147099,RMVar_hsa_circ_147100,RMVar_hsa_circ_147097,RMVar_hsa_circ_147094,RMVar_hsa_circ_147095,RMVar_hsa_circ_147093,RMVar_hsa_circ_147090,RMVar_hsa_circ_147091,RMVar_hsa_circ_147089,RMVar_hsa_circ_147084,RMVar_hsa_circ_147086,RMVar_hsa_circ_147087,RMVar_hsa_circ_147085,RMVar_hsa_circ_147082,RMVar_hsa_circ_147083,RMVar_hsa_circ_147081,RMVar_hsa_circ_147076,RMVar_hsa_circ_147078,RMVar_hsa_circ_147079,RMVar_hsa_circ_147077,RMVar_hsa_circ_147074,RMVar_hsa_circ_147075,RMVar_hsa_circ_147073,RMVar_hsa_circ_147064,RMVar_hsa_circ_147068,RMVar_hsa_circ_147070,RMVar_hsa_circ_147071,RMVar_hsa_circ_147069,RMVar_hsa_circ_147066,RMVar_hsa_circ_147067,RMVar_hsa_circ_147065,RMVar_hsa_circ_147060,RMVar_hsa_circ_147062,RMVar_hsa_circ_147063,RMVar_hsa_circ_147061,RMVar_hsa_circ_147058,RMVar_hsa_circ_147059 115523 RMVar_ID_115523 Human_SNP_ID_807097409 m1A Human chr10 - 87342925 87342925 87342925 CCCCGACCCGGATCCCGAGCTGCGTCGCGGACAATGCCGCGGGCCCGTCCCGGACTACGACTCCC CCCCGACCCGGATCCCGAGCTGCGTCGCGGACGATGCCGCGGGCCCGTCCCGGACTACGACTCCC T C NUTM2A-AS1 RNACentral:URS0000D59868 lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:87342890..87342957 26863196 MeRIP-seq:(Medium) rs1045091 Functional Loss SNV ICGC 33..33 33 COCA 1 - 115524 RMVar_ID_115524 Human_SNP_ID_807131711 m1A Human chr10 + 127100675 127100675 127100675 AAGGGGCTGGGGGAGCAGGGCCCTGCGCAGGGAGCTGGAAGGAGGGTGGAGAGGCAGGTGGCCAC AAGGGGCTGGGGGAGCAGGGCCCTGCGCAGGGTGCTGGAAGGAGGGTGGAGAGGCAGGTGGCCAC A T DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:127100536..127101287 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_123890,RMVar_hsa_circ_108908,RMVar_hsa_circ_356447,RMVar_hsa_circ_350151,RMVar_hsa_circ_335420,RMVar_hsa_circ_312465,RMVar_hsa_circ_126800,RMVar_hsa_circ_282287,RMVar_hsa_circ_119815,RMVar_hsa_circ_122922,RMVar_hsa_circ_119950,RMVar_hsa_circ_118430,RMVar_hsa_circ_119036,RMVar_hsa_circ_116315,RMVar_hsa_circ_83722,RMVar_hsa_circ_91893,RMVar_hsa_circ_99913,RMVar_hsa_circ_86451,RMVar_hsa_circ_85382,RMVar_hsa_circ_75989,RMVar_hsa_circ_78072,RMVar_hsa_circ_81059,RMVar_hsa_circ_77938,RMVar_hsa_circ_66778,RMVar_hsa_circ_75684,RMVar_hsa_circ_60900,RMVar_hsa_circ_147072,RMVar_hsa_circ_147099,RMVar_hsa_circ_147100,RMVar_hsa_circ_147076,RMVar_hsa_circ_147078,RMVar_hsa_circ_147077,RMVar_hsa_circ_147074,RMVar_hsa_circ_147075,RMVar_hsa_circ_147073,RMVar_hsa_circ_147064,RMVar_hsa_circ_147068,RMVar_hsa_circ_147070,RMVar_hsa_circ_147071,RMVar_hsa_circ_147069,RMVar_hsa_circ_147066,RMVar_hsa_circ_147067,RMVar_hsa_circ_147065,RMVar_hsa_circ_147060,RMVar_hsa_circ_147062,RMVar_hsa_circ_147063,RMVar_hsa_circ_147061,RMVar_hsa_circ_84588,RMVar_hsa_circ_147058,RMVar_hsa_circ_147059,RMVar_hsa_circ_147101,RMVar_hsa_circ_147105,RMVar_hsa_circ_87273,RMVar_hsa_circ_147106,RMVar_hsa_circ_99708,RMVar_hsa_circ_90391,RMVar_hsa_circ_147107,RMVar_hsa_circ_147108,RMVar_hsa_circ_101239,RMVar_hsa_circ_147110,RMVar_hsa_circ_120058,RMVar_hsa_circ_83966,RMVar_hsa_circ_126814,RMVar_hsa_circ_147112,RMVar_hsa_circ_373968,RMVar_hsa_circ_147116,RMVar_hsa_circ_83931,RMVar_hsa_circ_147117,RMVar_hsa_circ_147118,RMVar_hsa_circ_100948,RMVar_hsa_circ_147119,RMVar_hsa_circ_114893,RMVar_hsa_circ_91297,RMVar_hsa_circ_89888,RMVar_hsa_circ_147122,RMVar_hsa_circ_147120,RMVar_hsa_circ_147121,RMVar_hsa_circ_113319,RMVar_hsa_circ_147128,RMVar_hsa_circ_147129,RMVar_hsa_circ_121845,RMVar_hsa_circ_88328,RMVar_hsa_circ_124309,RMVar_hsa_circ_147130,RMVar_hsa_circ_147134,RMVar_hsa_circ_87901,RMVar_hsa_circ_147135,RMVar_hsa_circ_106570,RMVar_hsa_circ_147136,RMVar_hsa_circ_147140,RMVar_hsa_circ_75666,RMVar_hsa_circ_88838,RMVar_hsa_circ_147142,RMVar_hsa_circ_107618,RMVar_hsa_circ_78381,RMVar_hsa_circ_108984,RMVar_hsa_circ_147145,RMVar_hsa_circ_147146,RMVar_hsa_circ_147147,RMVar_hsa_circ_103029,RMVar_hsa_circ_147149,RMVar_hsa_circ_339567,RMVar_hsa_circ_117628,RMVar_hsa_circ_147150,RMVar_hsa_circ_126031,RMVar_hsa_circ_147154,RMVar_hsa_circ_347742,RMVar_hsa_circ_147152,RMVar_hsa_circ_355530,RMVar_hsa_circ_323726,RMVar_hsa_circ_333818,RMVar_hsa_circ_329649,RMVar_hsa_circ_271150,RMVar_hsa_circ_24573,RMVar_hsa_circ_104942,RMVar_hsa_circ_122049,RMVar_hsa_circ_103655,RMVar_hsa_circ_147156,RMVar_hsa_circ_147158,RMVar_hsa_circ_147160,RMVar_hsa_circ_147161,RMVar_hsa_circ_147159,RMVar_hsa_circ_147157,RMVar_hsa_circ_147155 115525 RMVar_ID_115525 Human_SNP_ID_807133615 m1A Human chr10 - 102133195 102133195 102133195 TCTCACCTGCTCGCCGCCGCTCACAGCGCCCAAAGTCCCATACGGCGCTTGGCTTCGACTTCCCC TCTCACCTGCTCGCCGCCGCTCACAGCGCCCACAGTCCCATACGGCGCTTGGCTTCGACTTCCCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:102133051..102133304 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - 115526 RMVar_ID_115526 Human_SNP_ID_807148990 m1A Human chr10 + 91633003 91633003 91633003 AGGCAGAGAGGCGGCGGACCCTAAAAGCCAGCACCCGCTGCCTGCACAAATTCGAACCACAGCTC AGGCAGAGAGGCGGCGGACCCTAAAAGCCAGCGCCCGCTGCCTGCACAAATTCGAACCACAGCTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:91632936..91633003 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 115527 RMVar_ID_115527 Human_SNP_ID_807183774 m1A Human chr10 - 119036201 119036201 119036201 GACCGGGTGGAAGAGCGGGACCCTCCTCGTCGAGTTCCTCCCCCAGCTCTTTCAAGAGACCGAGA GACCGGGTGGAAGAGCGGGACCCTCCTCGTCGTGTTCCTCCCCCAGCTCTTTCAAGAGACCGAGA T A EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119036151..119036290 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_26561,Human_RBP_ID_5935336,Human_RBP_ID_8758525,Human_RBP_ID_9254164,Human_RBP_ID_9360837,Human_RBP_ID_18587937,Human_RBP_ID_22886830,Human_RBP_ID_24542032,Human_RBP_ID_24785965,Human_RBP_ID_26316740,Human_RBP_ID_27803045 Human_Splice_Rec_1180970,Human_Splice_Rec_1181012 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614 115528 RMVar_ID_115528 Human_SNP_ID_807206070 m1A Human chr10 - 43387357 43387357 43387357 GAGAAGGCTCTAGGGAAACACAAGGAGAGGATAGGGCACAGGTACATTGAGGTGTTTAAGAGCAG GAGAAGGCTCTAGGGAAACACAAGGAGAGGATGGGGCACAGGTACATTGAGGTGTTTAAGAGCAG T C HNRNPF Ensembl:ENSG00000169813 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:43386998..43387943 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,lung adenocarcinoma,large_intestine adenocarcinoma,LUAD 13 lung,caecum,large intestine Human_RBP_ID_28027,Human_RBP_ID_1446789,Human_RBP_ID_2218034,Human_RBP_ID_5972186,Human_RBP_ID_8761057,Human_RBP_ID_9593696,Human_RBP_ID_11364109,Human_RBP_ID_17777508,Human_RBP_ID_18431750,Human_RBP_ID_27193102,Human_RBP_ID_27405838 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275 115529 RMVar_ID_115529 Human_SNP_ID_807230557 m1A Human chr10 + 17230705 17230705 17230705 GAGAGGAAGCCGAAAACACCCTGCAATCTTTCAGACAGGTTTGTAGACTCTCTTCCCACTCGCAG GAGAGGAAGCCGAAAACACCCTGCAATCTTTCGGACAGGTTTGTAGACTCTCTTCCCACTCGCAG A G VIM Ensembl:ENSG00000026025 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:17230596..17230757;chr10:17230651..17230725;chr10:17230650..17230750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_375082,Human_RBP_ID_1444884,Human_RBP_ID_8331136,Human_RBP_ID_8759919,Human_RBP_ID_8986292,Human_RBP_ID_17226391,Human_RBP_ID_17786679,Human_RBP_ID_22752369,Human_RBP_ID_27405159 Human_Splice_Rec_1115888,Human_Splice_Rec_1115889,Human_Splice_Rec_1115906,Human_Splice_Rec_1115907,Human_Splice_Rec_1115922,Human_Splice_Rec_1115923,Human_Splice_Rec_1115936,Human_Splice_Rec_1115937,Human_Splice_Rec_1115947,Human_Splice_Rec_1115953 Human_miRNA_ID_2700872 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_266472,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142429,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_112400,RMVar_hsa_circ_21781,RMVar_hsa_circ_40197,RMVar_hsa_circ_142434,RMVar_hsa_circ_142435 115530 RMVar_ID_115530 Human_SNP_ID_807246293 m1A Human chr10 - 17604002 17604001 17604002 GCTATTGCCATGGTACGTTTTTATATGGAAAAAGGAACACACAGAGGTTTATATAAAAGTATTCA GCTATTGCCATGGTACGTTTTTATATGGAAAA_GGAACACACAGAGGTTTATATAAAAGTATTCA CT C HACD1 Ensembl:ENSG00000165996 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:17603939..17604039 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_5951665 Human_Splice_Rec_1116032,Human_Splice_Rec_1116033,Human_Splice_Rec_1116054,Human_Splice_Rec_1116055,Human_Splice_Rec_1116062 RMVar_hsa_circ_142461,RMVar_hsa_circ_142463,RMVar_hsa_circ_142465,RMVar_hsa_circ_142464,RMVar_hsa_circ_377162,RMVar_hsa_circ_296986,RMVar_hsa_circ_115426,RMVar_hsa_circ_288232,RMVar_hsa_circ_142466,RMVar_hsa_circ_142467,RMVar_hsa_circ_142468,RMVar_hsa_circ_276120 115531 RMVar_ID_115531 Human_SNP_ID_807253135 m1A Human chr10 - 3082451 3082451 3082451 GGGGTGAGGGGCAGACACTGACCTCGTAGATGAAGTACACCTTGGCCCCCACGTAGATACCCATG GGGGTGAGGGGCAGACACTGACCTCGTAGATGTAGTACACCTTGGCCCCCACGTAGATACCCATG T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:3082401..3082475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 115532 RMVar_ID_115532 Human_SNP_ID_807277563 m1A Human chr10 - 128108036 128108036 128108036 CCAGTGGACACCCCAACAAGCACAAAGCAACGACCCAAGAGAAGTATCAGGAAAGCAGATGTAGA CCAGTGGACACCCCAACAAGCACAAAGCAACGGCCCAAGAGAAGTATCAGGAAAGCAGATGTAGA T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128107987..128108072 26863196 MeRIP-seq:(Medium) rs1437506182 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_27579,Human_RBP_ID_1763019,Human_RBP_ID_9321076,Human_RBP_ID_18410433,Human_RBP_ID_24542069,Human_RBP_ID_26876877 Human_miRNA_ID_3117655 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 115533 RMVar_ID_115533 Human_SNP_ID_807325396 m1A Human chr10 - 14585246 14585246 14585246 GAGGGTGTCCAGGTTCTTGGCATTTTGAACAAAGAATTGGACAAAACGCACAAACAAAGCAAGGA GAGGGTGTCCAGGTTCTTGGCATTTTGAACAAGGAATTGGACAAAACGCACAAACAAAGCAAGGA T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:14585244..14585421 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 115534 RMVar_ID_115534 Human_SNP_ID_807332252 m1A Human chr10 + 21517124 21517124 21517124 GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCAGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG GCGGCGGCGGCGGCGGCGGCGGCGGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGCTGCCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:21517122..21517284 26863196 MeRIP-seq:(Medium) rs868442911 Functional Loss SNV ICGC 33..33 33 STAD 1 - 115535 RMVar_ID_115535 Human_SNP_ID_807339891 m1A Human chr10 - 124461885 124461884 124461885 AGATGTCAAGCAGCACCCCGCGCACGCCAGCCAGCCGCTTGCCCCACGGTGCCATGGCGCCCGGC AGATGTCAAGCAGCACCCCGCGCACGCCAGCC_GCCGCTTGCCCCACGGTGCCATGGCGCCCGGC CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:124461826..124484183 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 LUAD 1 - 115536 RMVar_ID_115536 Human_SNP_ID_807352516 m1A Human chr10 - 77853403 77853403 77853403 GCAGCAGTCATGGGAGGACATGAAGCGGCTCCACGAGGAGGACCAGAAGGAGATCGGTGACCTCC GCAGCAGTCATGGGAGGACATGAAGCGGCTCCGCGAGGAGGACCAGAAGGAGATCGGTGACCTCC T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:77853354..77853576 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 1 breast Human_RBP_ID_862496,Human_RBP_ID_4128971,Human_RBP_ID_5520163,Human_RBP_ID_18970104,Human_RBP_ID_26317318,Human_RBP_ID_27802171 Human_Splice_Rec_1154317,Human_Splice_Rec_1154437 RMVar_hsa_circ_126566,RMVar_hsa_circ_94488,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144525,RMVar_hsa_circ_97814,RMVar_hsa_circ_144530,RMVar_hsa_circ_112890,RMVar_hsa_circ_116192,RMVar_hsa_circ_296916,RMVar_hsa_circ_144531,RMVar_hsa_circ_324307,RMVar_hsa_circ_291399,RMVar_hsa_circ_144533,RMVar_hsa_circ_144534,RMVar_hsa_circ_144535,RMVar_hsa_circ_144532 115537 RMVar_ID_115537 Human_SNP_ID_807356690 m1A Human chr10 + 79848571 79848571 79848571 AAGGCCCAGACTGCCTGCCTGCCACCACCCAGACCCCAGAGGCCAGTGACCAAGGCCCGCCGGCC AAGGCCCAGACTGCCTGCCTGCCACCACCCAGGCCCCAGAGGCCAGTGACCAAGGCCCGCCGGCC A G NUTM2E Ensembl:ENSG00000228570 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:79848521..79848607 26863196 MeRIP-seq:(Medium) rs382514 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_Splice_Rec_1155378,Human_Splice_Rec_1155388 115538 RMVar_ID_115538 Human_SNP_ID_807361575 m1A Human chr10 - 103368057 103368057 103368057 CGCCTGCGCCGTCCCCCGCCTGCGGAGGTAGCAGCGTTGGCGGTCCCTCAGGCTCTAGCTTGACC CGCCTGCGCCGTCCCCCGCCTGCGGAGGTAGCTGCGTTGGCGGTCCCTCAGGCTCTAGCTTGACC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:103368008..103368129 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 115539 RMVar_ID_115539 Human_SNP_ID_807373054 m1A Human chr10 + 87713188 87713187 87713189 TGGATGGGGACAATGTCCGTCATGGCCTTAACAGAAATCTCGGATTCTCTCCTGGGGACAGAGAG TGGATGGGGACAATGTCCGTCATGGCCTTAAC__AAATCTCGGATTCTCTCCTGGGGACAGAGAG CAG C PAPSS2 Ensembl:ENSG00000198682 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:87713138..87714071 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..34 33 HNSC 2 - Human_RBP_ID_384289,Human_RBP_ID_4130997 Human_miRNA_ID_424868,Human_miRNA_ID_2136651,Human_miRNA_ID_2665445 RMVar_hsa_circ_68976,RMVar_hsa_circ_274995,RMVar_hsa_circ_360680,RMVar_hsa_circ_289211,RMVar_hsa_circ_72048,RMVar_hsa_circ_144756 115540 RMVar_ID_115540 Human_SNP_ID_807415926 m1A Human chr10 - 23095627 23095627 23095627 AGGCGCAGTTCCGAGGGTCAGGCCCCGGAGCAACCAGAGGAGCCGCGCCATGACGCCCGCTCCGG AGGCGCAGTTCCGAGGGTCAGGCCCCGGAGCAGCCAGAGGAGCCGCGCCATGACGCCCGCTCCGG T C AL139815.1 Ensembl:ENSG00000286924 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:23095576..23110262;chr10:23095576..23104250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115541 RMVar_ID_115541 Human_SNP_ID_807433352 m1A Human chr10 + 46285015 46285015 46285015 CCGTGGACCCCCGCGGCCTCCCGGCCTTCCTTACCCCGGCGGCCTGGCGGCCCCGCGAGCTTCAC CCGTGGACCCCCGCGGCCTCCCGGCCTTCCTTCCCCCGGCGGCCTGGCGGCCCCGCGAGCTTCAC A C LOC105378577,LOC105378577:2 RNACentral:URS0000E60AD6,RNACentral:URS000029E2A0 lincRNA,lincRNA exon,exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:46284964..46285078 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115542 RMVar_ID_115542 Human_SNP_ID_807465237 m1A Human chr10 - 133369953 133369953 133369953 TTACTCCAGCAAGTTCTTGAAGCACTGGGACCACCTCACCCAGGTCAAGAAGCCAGTCATCGCTG TTACTCCAGCAAGTTCTTGAAGCACTGGGACCGCCTCACCCAGGTCAAGAAGCCAGTCATCGCTG T C ECHS1 Ensembl:ENSG00000127884 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:133369901..133370050 32194978 MeRIP-seq:(Medium) rs769170809 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_374358,Human_RBP_ID_1444334,Human_RBP_ID_8330138 Human_Splice_Rec_1191328,Human_Splice_Rec_1191329 Human_miRNA_ID_2007036 RMVar_hsa_circ_12978,RMVar_hsa_circ_106076,RMVar_hsa_circ_116135,RMVar_hsa_circ_81001,RMVar_hsa_circ_147321,RMVar_hsa_circ_147322,RMVar_hsa_circ_147320,RMVar_hsa_circ_103177,RMVar_hsa_circ_147323 115543 RMVar_ID_115543 Human_SNP_ID_807491366 m1A Human chr10 + 91162960 91162960 91162960 GGCCGGCCCAGCCCCCGCCCCGCGCCGCTCGCACCCCCGCTGCCCCGCCCCGCCCCCGCCGGCGC GGCCGGCCCAGCCCCCGCCCCGCGCCGCTCGCCCCCCCGCTGCCCCGCCCCGCCCCCGCCGGCGC A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:91162932..91163101 26863196 MeRIP-seq:(Medium) rs1460161593 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115544 RMVar_ID_115544 Human_SNP_ID_807498087 m1A Human chr10 + 1592579 1592579 1592579 ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCAAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT ATGGTCCCCTCTGTCACCCAGCTCCCTTCGCCCAAGCCACCCTCCATAGGTCTCCTCTCTGGCAT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1592536..1592620 26863196 MeRIP-seq:(Medium) rs34546595 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver 115545 RMVar_ID_115545 Human_SNP_ID_807508118 m1A Human chr10 + 103691727 103691727 103691727 ACACAAATACACACAAACACAGACTCCAACCCATAACCAGATATATCTCAACCACACACACACCC ACACAAATACACACAAACACAGACTCCAACCCTTAACCAGATATATCTCAACCACACACACACCC A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:103691717..103691903 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 115546 RMVar_ID_115546 Human_SNP_ID_807534835 m1A Human chr10 + 17229664 17229664 17229664 GCGGAGCAGCGTGCCCGGGGTGCGGCTCCTGCAGGACTCGGTGGACTTCTCGCTGGCCGACGCCA GCGGAGCAGCGTGCCCGGGGTGCGGCTCCTGCTGGACTCGGTGGACTTCTCGCTGGCCGACGCCA A T VIM Ensembl:ENSG00000026025 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_26050,Human_RBP_ID_224967,Human_RBP_ID_375069,Human_RBP_ID_746966,Human_RBP_ID_982533,Human_RBP_ID_4114875,Human_RBP_ID_5459167,Human_RBP_ID_5951563,Human_RBP_ID_8055849,Human_RBP_ID_8331128,Human_RBP_ID_8759907,Human_RBP_ID_8986290,Human_RBP_ID_9272657,Human_RBP_ID_17679793,Human_RBP_ID_17774118,Human_RBP_ID_18187909,Human_RBP_ID_22377295,Human_RBP_ID_22431382,Human_RBP_ID_22752368,Human_RBP_ID_23123507,Human_RBP_ID_27153734,Human_RBP_ID_27192255,Human_RBP_ID_27405145,Human_RBP_ID_27556102 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_266472,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142429,RMVar_hsa_circ_142426 115547 RMVar_ID_115547 Human_SNP_ID_807553419 m1A Human chr10 + 31461049 31461049 31461049 GTTTCTTGTTTGTATTACAGTTACAAATTATAATACTGTGGTAGAAACAAATTCAGATTCAGATG GTTTCTTGTTTGTATTACAGTTACAAATTATATTACTGTGGTAGAAACAAATTCAGATTCAGATG A T ZEB1 Ensembl:ENSG00000148516 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31461025..31502354 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_8333186,Human_RBP_ID_8760555,Human_RBP_ID_22788085 Human_Splice_Rec_1122972,Human_Splice_Rec_1122992,Human_Splice_Rec_1122998,Human_Splice_Rec_1123020,Human_Splice_Rec_1123030,Human_Splice_Rec_1123046,Human_Splice_Rec_1123064,Human_Splice_Rec_1123078,Human_Splice_Rec_1123092,Human_Splice_Rec_1123100,Human_Splice_Rec_1123116,Human_Splice_Rec_1123158,Human_Splice_Rec_1123170,Human_Splice_Rec_1123186,Human_Splice_Rec_1123200,Human_Splice_Rec_1123210,Human_Splice_Rec_1123226,Human_Splice_Rec_1123240,Human_Splice_Rec_1123250,Human_Splice_Rec_1123256,Human_Splice_Rec_1123274,Human_Splice_Rec_1123282 Human_miRNA_ID_159391,Human_miRNA_ID_304524,Human_miRNA_ID_2055696,Human_miRNA_ID_2055697,Human_miRNA_ID_2067294,Human_miRNA_ID_2067295 RMVar_hsa_circ_87610,RMVar_hsa_circ_360534,RMVar_hsa_circ_142930,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_142942,RMVar_hsa_circ_298968,RMVar_hsa_circ_142946,RMVar_hsa_circ_292700,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941,RMVar_hsa_circ_41010,RMVar_hsa_circ_277204,RMVar_hsa_circ_352540,RMVar_hsa_circ_362863,RMVar_hsa_circ_293595,RMVar_hsa_circ_274481,RMVar_hsa_circ_142947 115548 RMVar_ID_115548 Human_SNP_ID_807553437 m1A Human chr10 + 31461049 31461049 31461049 GTTTCTTGTTTGTATTACAGTTACAAATTATAATACTGTGGTAGAAACAAATTCAGATTCAGATG GTTTCTTGTTTGTATTACAGTTACAAATTATAGTACTGTGGTAGAAACAAATTCAGATTCAGATG A G ZEB1 Ensembl:ENSG00000148516 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31461025..31502354 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_8333186,Human_RBP_ID_8760555,Human_RBP_ID_22788085 Human_Splice_Rec_1122972,Human_Splice_Rec_1122992,Human_Splice_Rec_1122998,Human_Splice_Rec_1123020,Human_Splice_Rec_1123030,Human_Splice_Rec_1123046,Human_Splice_Rec_1123064,Human_Splice_Rec_1123078,Human_Splice_Rec_1123092,Human_Splice_Rec_1123100,Human_Splice_Rec_1123116,Human_Splice_Rec_1123158,Human_Splice_Rec_1123170,Human_Splice_Rec_1123186,Human_Splice_Rec_1123200,Human_Splice_Rec_1123210,Human_Splice_Rec_1123226,Human_Splice_Rec_1123240,Human_Splice_Rec_1123250,Human_Splice_Rec_1123256,Human_Splice_Rec_1123274,Human_Splice_Rec_1123282 Human_miRNA_ID_159391,Human_miRNA_ID_304524,Human_miRNA_ID_2055696,Human_miRNA_ID_2055697,Human_miRNA_ID_2067294,Human_miRNA_ID_2067295 RMVar_hsa_circ_87610,RMVar_hsa_circ_360534,RMVar_hsa_circ_142930,RMVar_hsa_circ_316878,RMVar_hsa_circ_31962,RMVar_hsa_circ_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_26726,RMVar_hsa_circ_142942,RMVar_hsa_circ_298968,RMVar_hsa_circ_142946,RMVar_hsa_circ_292700,RMVar_hsa_circ_325277,RMVar_hsa_circ_343353,RMVar_hsa_circ_16941,RMVar_hsa_circ_41010,RMVar_hsa_circ_277204,RMVar_hsa_circ_352540,RMVar_hsa_circ_362863,RMVar_hsa_circ_293595,RMVar_hsa_circ_274481,RMVar_hsa_circ_142947 115549 RMVar_ID_115549 Human_SNP_ID_807565212 m1A Human chr10 + 59906271 59906271 59906271 GCGGTTGGTGAGCTCCTCCAGGCGGAACGGCGAGATGACAATGCCCCCCGACTTCCCACCGCCGC GCGGTTGGTGAGCTCCTCCAGGCGGAACGGCGCGATGACAATGCCCCCCGACTTCCCACCGCCGC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:59906126..59906540 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma,breast lobular_carcinoma 4 breast 115550 RMVar_ID_115550 Human_SNP_ID_807574940 m1A Human chr10 - 587210 587210 587210 CCCCTCGCCACGCTGTCAGCAGGGACCCGGGTAGTCTGGCCTTAGACCCTGCACTGTTTGCCCCT CCCCTCGCCACGCTGTCAGCAGGGACCCGGGTGGTCTGGCCTTAGACCCTGCACTGTTTGCCCCT T C DIP2C Ensembl:ENSG00000151240 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:587207..587359 32194978 MeRIP-seq:(Medium) rs570470559 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_23462223 115551 RMVar_ID_115551 Human_SNP_ID_807604012 m1A Human chr10 - 5888066 5888066 5888066 CCATCTGACAGCTTCTCCTGGTTGGCCTTAGGACTCCTCTGATGATGGCCTGCACAAGGAAGAAC CCATCTGACAGCTTCTCCTGGTTGGCCTTAGGCCTCCTCTGATGATGGCCTGCACAAGGAAGAAC T G ANKRD16 Ensembl:ENSG00000134461 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:5888044..5889215 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_862096,Human_RBP_ID_18970572,Human_RBP_ID_22639134 Human_Splice_Rec_1108872,Human_Splice_Rec_1108886,Human_Splice_Rec_1108898 RMVar_hsa_circ_338981,RMVar_hsa_circ_19465 115552 RMVar_ID_115552 Human_SNP_ID_807718786 m1A Human chr10 + 29686649 29686649 29686649 TTTAGAAAGCAACCAATCTCCAATGTAGCCAGAATCTGGGGGAGAAAAGTTTTAAAAAAATCATA TTTAGAAAGCAACCAATCTCCAATGTAGCCAGTATCTGGGGGAGAAAAGTTTTAAAAAAATCATA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:29686610..29686700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115553 RMVar_ID_115553 Human_SNP_ID_807721127 m1A Human chr10 - 32929938 32929938 32929938 TCCAGATGACATAGAAAATCCCAGAGGCTCCAAAGATATAAAGAAAAATAAAAATGTAACCAACC TCCAGATGACATAGAAAATCCCAGAGGCTCCAGAGATATAAAGAAAAATAAAAATGTAACCAACC T C ITGB1 Ensembl:ENSG00000150093 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:32929887..32929989 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_2215126,Human_RBP_ID_17776434,Human_RBP_ID_19452570,Human_RBP_ID_22377547,Human_RBP_ID_23454030,Human_RBP_ID_24456922 Human_Splice_Rec_1124287 RMVar_hsa_circ_28433,RMVar_hsa_circ_76607,RMVar_hsa_circ_328275,RMVar_hsa_circ_270269,RMVar_hsa_circ_105283,RMVar_hsa_circ_143078,RMVar_hsa_circ_51605,RMVar_hsa_circ_68140,RMVar_hsa_circ_143080,RMVar_hsa_circ_289320,RMVar_hsa_circ_366400,RMVar_hsa_circ_361090,RMVar_hsa_circ_143081,RMVar_hsa_circ_335192,RMVar_hsa_circ_374394,RMVar_hsa_circ_143082,RMVar_hsa_circ_65919,RMVar_hsa_circ_143086,RMVar_hsa_circ_143083,RMVar_hsa_circ_368899,RMVar_hsa_circ_358985,RMVar_hsa_circ_35572,RMVar_hsa_circ_57460,RMVar_hsa_circ_365912,RMVar_hsa_circ_349797,RMVar_hsa_circ_16114,RMVar_hsa_circ_65921 115554 RMVar_ID_115554 Human_SNP_ID_807743078 m1A Human chr10 + 41857075 41857075 41857075 GGAATGCAATGGTATGGAATGGAGTCAAACCGAGTGGAATGGAATGGAATGGAATGGAATAAATG GGAATGCAATGGTATGGAATGGAGTCAAACCGCGTGGAATGGAATGGAATGGAATGGAATAAATG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:41857013..41857116 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 115555 RMVar_ID_115555 Human_SNP_ID_807750304 m1A Human chr10 - 52455230 52455230 52455230 ATGTTAGAGAGATGACAGAGTCTAGGTTAGGGAGGGCCTGAGTCCTTGTAGACTCTGAGTACGGT ATGTTAGAGAGATGACAGAGTCTAGGTTAGGGTGGGCCTGAGTCCTTGTAGACTCTGAGTACGGT T A LNCAROD Ensembl:ENSG00000231131 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:52455152..52455269 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_miRNA_ID_3195114 115556 RMVar_ID_115556 Human_SNP_ID_807758305 m1A Human chr10 - 27111037 27111036 27111037 AAAAATTAAAATAAATTTAAATACAAAAAAAAATAGCCAGGTGTGGGGTGCATGCCTGGAATCCC AAAAATTAAAATAAATTTAAATACAAAAAAAA_TAGCCAGGTGTGGGGTGCATGCCTGGAATCCC AT A YME1L1 Ensembl:ENSG00000136758 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1207223401 Functional Loss DEL ICGC 33..33 33 COCA 1 - Human_RBP_ID_4141019,Human_RBP_ID_5958730,Human_RBP_ID_8172580,Human_RBP_ID_8332372,Human_RBP_ID_24803106 115557 RMVar_ID_115557 Human_SNP_ID_807800317 m1A Human chr10 - 117375227 117375227 117375227 GGAGTAGGGGCCCGGGCGGAGGCGGTGGCGGGATGGGGCTGCTGCTCATGATCCTGGCGTCGGCC GGAGTAGGGGCCCGGGCGGAGGCGGTGGCGGGCTGGGGCTGCTGCTCATGATCCTGGCGTCGGCC T G PDZD8 Ensembl:ENSG00000165650 Protein coding start codon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:117375180..117375423 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_4108694,Human_RBP_ID_5933274,Human_RBP_ID_8765472,Human_RBP_ID_9274268,Human_RBP_ID_17770764,Human_RBP_ID_18431311 115558 RMVar_ID_115558 Human_SNP_ID_807821323 m1A Human chr10 + 42796699 42796699 42796699 GATCAGTATATGGCTGTTAAGGGCATCAAACGACGGAAACTTGAGTTGGAAGAAGACAGTGAAAT GATCAGTATATGGCTGTTAAGGGCATCAAACGGCGGAAACTTGAGTTGGAAGAAGACAGTGAAAT A G BMS1 Ensembl:ENSG00000165733 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:42796601..42796792 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 2 stomach Human_RBP_ID_1766758 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_119914,RMVar_hsa_circ_43537,RMVar_hsa_circ_90499,RMVar_hsa_circ_143233,RMVar_hsa_circ_103201,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_28584,RMVar_hsa_circ_143234,RMVar_hsa_circ_143236,RMVar_hsa_circ_143237,RMVar_hsa_circ_143235,RMVar_hsa_circ_30730,RMVar_hsa_circ_83308,RMVar_hsa_circ_59285,RMVar_hsa_circ_100425,RMVar_hsa_circ_143239,RMVar_hsa_circ_353251,RMVar_hsa_circ_34535,RMVar_hsa_circ_143240,RMVar_hsa_circ_143241 115559 RMVar_ID_115559 Human_SNP_ID_807850624 m1A Human chr10 + 113854723 113854722 113854723 ATTTGGACTTTTGGCACTTGGACCTATGCTTTAAAAAGAAAAAAGTGTCATTGGCGTGGAGTGGG ATTTGGACTTTTGGCACTTGGACCTATGCTTT_AAAAGAAAAAAGTGTCATTGGCGTGGAGTGGG TA T NHLRC2 Ensembl:ENSG00000196865 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:113854673..113854825 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - Human_RBP_ID_4107575,Human_RBP_ID_18416188,Human_RBP_ID_18587238,Human_RBP_ID_26874921 115560 RMVar_ID_115560 Human_SNP_ID_807898025 m1A Human chr10 + 132573987 132573987 132573987 CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTACGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG CCGTGTGAGGTTTTGTTGAGATGTTGGGGTGTGCGTGCCGTGGGAGGTTTTGTTGAGATGTTGGG A G INPP5A Ensembl:ENSG00000068383 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:132573968..132574037 26863196 MeRIP-seq:(Medium) rs2814441 Functional Loss SNV COSMIC 33..33 33 brain large_cell,central_nervous_system large_cell 2 brain RMVar_hsa_circ_111133,RMVar_hsa_circ_124149,RMVar_hsa_circ_147264,RMVar_hsa_circ_147265 115561 RMVar_ID_115561 Human_SNP_ID_807943158 m1A Human chr10 - 119898467 119898467 119898467 GTCTGTGGGGCAGATGTGTGAATAGAAGTCTGACCAAGGAAGCTGTCCTCCTCACCAACATCTGT GTCTGTGGGGCAGATGTGTGAATAGAAGTCTGGCCAAGGAAGCTGTCCTCCTCACCAACATCTGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:119898434..119898578 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115562 RMVar_ID_115562 Human_SNP_ID_807945694 m1A Human chr10 + 133373302 133373302 133373302 GACAGCGAACCGGGGGCCTCAGCGGGCCGCGGACGCAGGACAGCAGGACACGCAGGGCGGCCATG GACAGCGAACCGGGGGCCTCAGCGGGCCGCGGGCGCAGGACAGCAGGACACGCAGGGCGGCCATG A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:133373215..133373686 26863196 MeRIP-seq:(Medium) rs10466126 Functional Loss SNV COSMIC 33..33 33 cerebellum ependymoma,thyroid neoplasm,colon adenocarcinoma,caecum adenocarcinoma,rectum adenocarcinoma,central_nervous_system ependymoma,large_intestine adenocarcinoma 12 caecum,head and neck,large intestine,brain 115563 RMVar_ID_115563 Human_SNP_ID_807947272 m1A Human chr10 - 101002822 101002822 101002822 CACTGCTTGGGCTGGGGGGTGACTCTGTCCGGAAGTCCTCATTGATGTAGGTGAAGCTGGTGACA CACTGCTTGGGCTGGGGGGTGACTCTGTCCGGCAGTCCTCATTGATGTAGGTGAAGCTGGTGACA T G lnc-PDZD7-1 RNACentral:URS00008BF54D lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:101002496..101002902 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 115564 RMVar_ID_115564 Human_SNP_ID_807969280 m1A Human chr10 + 17229386 17229386 17229386 GTTCGCCTCTTCTCCGGGAGCCAGTCCGCGCCACCGCCGCCGCCCAGGCCATCGCCACCCTCCGC GTTCGCCTCTTCTCCGGGAGCCAGTCCGCGCCGCCGCCGCCGCCCAGGCCATCGCCACCCTCCGC A G VIM Ensembl:ENSG00000026025 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:17229276..17229978 26863196 MeRIP-seq:(Medium) rs1564372087 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_224965,Human_RBP_ID_1763819,Human_RBP_ID_4136178,Human_RBP_ID_5415003,Human_RBP_ID_5435286,Human_RBP_ID_8759903,Human_RBP_ID_17226384,Human_RBP_ID_17345580,Human_RBP_ID_17774117,Human_RBP_ID_22532201 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_119034,RMVar_hsa_circ_142424,RMVar_hsa_circ_142425,RMVar_hsa_circ_126545,RMVar_hsa_circ_266472,RMVar_hsa_circ_142427,RMVar_hsa_circ_120723,RMVar_hsa_circ_142428,RMVar_hsa_circ_142429,RMVar_hsa_circ_142426 115565 RMVar_ID_115565 Human_SNP_ID_807972034 m1A Human chr10 - 75401201 75401201 75401201 TCTGACCCCCTGCGCCAGGCCAACCGCCTGCCAATCAAGGTGCTGAAGATGCTGACGGCACGAAC TCTGACCCCCTGCGCCAGGCCAACCGCCTGCCCATCAAGGTGCTGAAGATGCTGACGGCACGAAC T G AC010997.3,ZNF503 Ensembl:ENSG00000270087,Ensembl:ENSG00000165655 lincRNA,Protein coding exon,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75401151..75401366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 HNSC,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_225613,Human_RBP_ID_985427,Human_RBP_ID_1450327,Human_RBP_ID_4136858,Human_RBP_ID_5459488,Human_RBP_ID_17783078,Human_RBP_ID_22156062,Human_RBP_ID_22490352,Human_RBP_ID_22788791,Human_RBP_ID_27195343,Human_RBP_ID_27407312 Human_Splice_Rec_1149985,Human_Splice_Rec_1149997 115566 RMVar_ID_115566 Human_SNP_ID_807995765 m1A Human chr10 + 113044975 113044975 113044975 TGGCAGTGGGGATGGTGAAAATAGAGATGTGGAGGAAACAGCAGCGGAACTTGCTGACAGGTTAG TGGCAGTGGGGATGGTGAAAATAGAGATGTGGGGGAAACAGCAGCGGAACTTGCTGACAGGTTAG A G TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:113044925..113045098 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 14 oesophagus Human_RBP_ID_11265224 RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 115567 RMVar_ID_115567 Human_SNP_ID_808027636 m1A Human chr10 - 59792958 59792958 59792958 CCACGGTCCCCTCAGCAGCCACCTCGCAGCCTACTCCTTCGCAACATTCGGCGCACCCCTCCTCC CCACGGTCCCCTCAGCAGCCACCTCGCAGCCTGCTCCTTCGCAACATTCGGCGCACCCCTCCTCC T C CCDC6 Ensembl:ENSG00000108091 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:59792907..59793100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_5982427,Human_RBP_ID_17227487,Human_RBP_ID_17344085,Human_RBP_ID_17460140,Human_RBP_ID_17779493 115568 RMVar_ID_115568 Human_SNP_ID_808049815 m1A Human chr10 + 73247220 73247217 73247221 ATGCCGGGCGGAGATACGACCCCGGAGGAAGCAGCCGCTCCCAGCTGCGCCGGGTACAACCCAGG ATGCCGGGCGGAGATACGACCCCGGAGGAA____CCGCTCCCAGCTGCGCCGGGTACAACCCAGG AGCAG A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73246988..73247275 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 MALY 1 - 115569 RMVar_ID_115569 Human_SNP_ID_808070772 m1A Human chr10 - 71817352 71817352 71817352 TGTCTGGGGGAATGAACGCACAGATCTGTTTGACTTTGTTATAAAAATAGGGCTCCCCCACCTCC TGTCTGGGGGAATGAACGCACAGATCTGTTTGGCTTTGTTATAAAAATAGGGCTCCCCCACCTCC T C PSAP Ensembl:ENSG00000197746 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:71817301..71817500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_381625,Human_RBP_ID_1449415,Human_RBP_ID_1770030,Human_RBP_ID_2229316,Human_RBP_ID_3356000,Human_RBP_ID_4126141,Human_RBP_ID_5110200,Human_RBP_ID_5137875,Human_RBP_ID_5164043,Human_RBP_ID_5545784,Human_RBP_ID_5994961,Human_RBP_ID_8338164,Human_RBP_ID_8991765,Human_RBP_ID_9273870,Human_RBP_ID_11413597,Human_RBP_ID_17183371,Human_RBP_ID_17647915,Human_RBP_ID_17680555,Human_RBP_ID_18243656,Human_RBP_ID_19452992,Human_RBP_ID_22378026,Human_RBP_ID_22887738,Human_RBP_ID_23152671,Human_RBP_ID_23206448,Human_RBP_ID_23467134,Human_RBP_ID_24401499,Human_RBP_ID_24457482,Human_RBP_ID_24829619,Human_RBP_ID_26396377,Human_RBP_ID_27194721,Human_RBP_ID_27556299 Human_miRNA_ID_647918,Human_miRNA_ID_1644901,Human_miRNA_ID_1650419,Human_miRNA_ID_1758296 RMVar_hsa_circ_85697,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_91301,RMVar_hsa_circ_100972,RMVar_hsa_circ_88171,RMVar_hsa_circ_144117,RMVar_hsa_circ_144121,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144123,RMVar_hsa_circ_81755,RMVar_hsa_circ_144124,RMVar_hsa_circ_144122,RMVar_hsa_circ_144119,RMVar_hsa_circ_144120,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114 115570 RMVar_ID_115570 Human_SNP_ID_808070776 m1A Human chr10 - 71817352 71817352 71817352 TGTCTGGGGGAATGAACGCACAGATCTGTTTGACTTTGTTATAAAAATAGGGCTCCCCCACCTCC TGTCTGGGGGAATGAACGCACAGATCTGTTTGTCTTTGTTATAAAAATAGGGCTCCCCCACCTCC T A PSAP Ensembl:ENSG00000197746 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:71817301..71817500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 KIRC 1 - Human_RBP_ID_381625,Human_RBP_ID_1449415,Human_RBP_ID_1770030,Human_RBP_ID_2229316,Human_RBP_ID_3356000,Human_RBP_ID_4126141,Human_RBP_ID_5110200,Human_RBP_ID_5137875,Human_RBP_ID_5164043,Human_RBP_ID_5545784,Human_RBP_ID_5994961,Human_RBP_ID_8338164,Human_RBP_ID_8991765,Human_RBP_ID_9273870,Human_RBP_ID_11413597,Human_RBP_ID_17183371,Human_RBP_ID_17647915,Human_RBP_ID_17680555,Human_RBP_ID_18243656,Human_RBP_ID_19452992,Human_RBP_ID_22378026,Human_RBP_ID_22887738,Human_RBP_ID_23152671,Human_RBP_ID_23206448,Human_RBP_ID_23467134,Human_RBP_ID_24401499,Human_RBP_ID_24457482,Human_RBP_ID_24829619,Human_RBP_ID_26396377,Human_RBP_ID_27194721,Human_RBP_ID_27556299 Human_miRNA_ID_647918,Human_miRNA_ID_1644901,Human_miRNA_ID_1650419,Human_miRNA_ID_1758296 RMVar_hsa_circ_85697,RMVar_hsa_circ_102323,RMVar_hsa_circ_116761,RMVar_hsa_circ_118928,RMVar_hsa_circ_111854,RMVar_hsa_circ_91301,RMVar_hsa_circ_100972,RMVar_hsa_circ_88171,RMVar_hsa_circ_144117,RMVar_hsa_circ_144121,RMVar_hsa_circ_83219,RMVar_hsa_circ_83912,RMVar_hsa_circ_144123,RMVar_hsa_circ_81755,RMVar_hsa_circ_144124,RMVar_hsa_circ_144122,RMVar_hsa_circ_144119,RMVar_hsa_circ_144120,RMVar_hsa_circ_144118,RMVar_hsa_circ_144115,RMVar_hsa_circ_144116,RMVar_hsa_circ_144114 115571 RMVar_ID_115571 Human_SNP_ID_808134683 m1A Human chr10 + 996237 996237 996237 CAAGAGGCAGAAGCAGAGTTTGGAGTATTTGGAGCAAGGTGCTTGTCACGCATCCGCGGGAACCG CAAGAGGCAGAAGCAGAGTTTGGAGTATTTGGGGCAAGGTGCTTGTCACGCATCCGCGGGAACCG A G GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:992634..996277 32194978 MeRIP-seq:(Medium) rs1414831594 Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_861056,Human_RBP_ID_1440681,Human_RBP_ID_5920245,Human_RBP_ID_9360056,Human_RBP_ID_11243980,Human_RBP_ID_23430757 Human_Splice_Rec_1106535,Human_Splice_Rec_1106585 RMVar_hsa_circ_5835,RMVar_hsa_circ_302583,RMVar_hsa_circ_336595,RMVar_hsa_circ_280435,RMVar_hsa_circ_289665,RMVar_hsa_circ_107063,RMVar_hsa_circ_78785,RMVar_hsa_circ_141547,RMVar_hsa_circ_141548,RMVar_hsa_circ_141549,RMVar_hsa_circ_304483,RMVar_hsa_circ_141546,RMVar_hsa_circ_141550,RMVar_hsa_circ_141551,RMVar_hsa_circ_46618 115572 RMVar_ID_115572 Human_SNP_ID_808151609 m1A Human chr10 - 125039061 125039061 125039061 TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCATAAAGAATGGCCCTTGTGGATAAGCACAAAGT TTTGCCTTTTGATCTGAGAGTTGCAAAGTTCCCTAAAGAATGGCCCTTGTGGATAAGCACAAAGT T G CTBP2 Ensembl:ENSG00000175029 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:125039011..125039200 26863196 MeRIP-seq:(Medium) rs76319950 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 10 liver Human_RBP_ID_1443473,Human_RBP_ID_8328940,Human_RBP_ID_18589602 Human_Splice_Rec_1186602,Human_Splice_Rec_1186603,Human_Splice_Rec_1186638,Human_Splice_Rec_1186639,Human_Splice_Rec_1186658,Human_Splice_Rec_1186659,Human_Splice_Rec_1186678,Human_Splice_Rec_1186679,Human_Splice_Rec_1186708,Human_Splice_Rec_1186709,Human_Splice_Rec_1186716,Human_Splice_Rec_1186722 RMVar_hsa_circ_103784,RMVar_hsa_circ_110012,RMVar_hsa_circ_88110,RMVar_hsa_circ_147000,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002,RMVar_hsa_circ_110716,RMVar_hsa_circ_147003,RMVar_hsa_circ_47244,RMVar_hsa_circ_147004,RMVar_hsa_circ_125557,RMVar_hsa_circ_62045,RMVar_hsa_circ_80631,RMVar_hsa_circ_272393,RMVar_hsa_circ_286734,RMVar_hsa_circ_147005,RMVar_hsa_circ_280237,RMVar_hsa_circ_126097,RMVar_hsa_circ_147007,RMVar_hsa_circ_147009,RMVar_hsa_circ_147011,RMVar_hsa_circ_98565,RMVar_hsa_circ_147010,RMVar_hsa_circ_147008,RMVar_hsa_circ_147006 115573 RMVar_ID_115573 Human_SNP_ID_808155394 m1A Human chr10 + 115000509 115000505 115000509 GAAAGAAGAAAGAGACAAAGAAAGAAAGAGAGAAGGAAAGAAAGGAAGGAAGGAAGAGAAGGAAG GAAAGAAGAAAGAGACAAAGAAAGAAAGA____AGGAAAGAAAGGAAGGAAGGAAGAGAAGGAAG AGAGA A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:115000441..115000588 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 LMS 1 - 115574 RMVar_ID_115574 Human_SNP_ID_808178346 m1A Human chr10 - 102111538 102111520 102111539 GCGCCCAGCTATGACTCCTTTCTTTCTCGTCTAGGTTGTTCCTCAAAGTCATTCAAGCTGTACTC GCGCCCAGCTATGACTCCTTTCTTTCTCGTC___________________ATTCAAGCTGTACTC TGACTTTGAGGAACAACCTA T LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:102111448..102114667 26863410 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..50 33 OV 1 - Human_RBP_ID_22639642 115575 RMVar_ID_115575 Human_SNP_ID_808219132 m1A Human chr10 - 113141263 113141263 113141263 CTGGTAAGTGTGGAGGTGGGTTTCCCGGCGTGAAGTGTTCATTGCTGTACGTGATAAGAGGCGTG CTGGTAAGTGTGGAGGTGGGTTTCCCGGCGTGGAGTGTTCATTGCTGTACGTGATAAGAGGCGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:113141213..113150990 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 15 lung 115576 RMVar_ID_115576 Human_SNP_ID_808229576 m1A Human chr10 - 119042740 119042740 119042740 GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGACAGGTCTCATAGAAGAGATGAAGAGCGGCCCC GGAGTGGAGACGTGGAGAAGGGCGAGATGAGGGCAGGTCTCATAGAAGAGATGAAGAGCGGCCCC T C EIF3A Ensembl:ENSG00000107581 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:119042640..119042756 26863196 MeRIP-seq:(Medium) rs369943865 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 haematopoietic and lymphoid tissue Human_RBP_ID_225081,Human_RBP_ID_747172,Human_RBP_ID_805724,Human_RBP_ID_864046,Human_RBP_ID_4139356,Human_RBP_ID_5935383,Human_RBP_ID_8758564,Human_RBP_ID_9360850,Human_RBP_ID_11278338,Human_RBP_ID_18410350,Human_RBP_ID_22029576,Human_RBP_ID_22886834,Human_RBP_ID_23481380,Human_RBP_ID_24542041,Human_RBP_ID_26315993,Human_RBP_ID_27802398 Human_Splice_Rec_1180964,Human_Splice_Rec_1181006 Human_miRNA_ID_3079722 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_61099,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_313961,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617,RMVar_hsa_circ_49267,RMVar_hsa_circ_328467 115577 RMVar_ID_115577 Human_SNP_ID_808252497 m1A Human chr10 - 50332186 50332186 50332186 GGTCATTGGGCTGAGATAGAGCCTGGAGAATGATAGGGAGGGTGGCCAGAGGGCAGGCTAGAGGG GGTCATTGGGCTGAGATAGAGCCTGGAGAATGTTAGGGAGGGTGGCCAGAGGGCAGGCTAGAGGG T A SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:50332151..50332362 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_115717,RMVar_hsa_circ_120183,RMVar_hsa_circ_269091,RMVar_hsa_circ_143419,RMVar_hsa_circ_143420,RMVar_hsa_circ_25980,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_143423,RMVar_hsa_circ_271876,RMVar_hsa_circ_373831,RMVar_hsa_circ_378622,RMVar_hsa_circ_25269,RMVar_hsa_circ_143422 115578 RMVar_ID_115578 Human_SNP_ID_808272421 m1A Human chr10 + 23104194 23104193 23104194 AGCTGCCTCTTGCCAAGAGTGAGTGGCAAAAGAAACTAACCCCGGAGCAGTTCTACGTCACAAGA AGCTGCCTCTTGCCAAGAGTGAGTGGCAAAAG_AACTAACCCCGGAGCAGTTCTACGTCACAAGA GA G MSRB2 Ensembl:ENSG00000148450 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:23104066..23104250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_4137210 Human_Splice_Rec_1118580,Human_Splice_Rec_1118581,Human_Splice_Rec_1118587 RMVar_hsa_circ_142649,RMVar_hsa_circ_322922,RMVar_hsa_circ_315020 115579 RMVar_ID_115579 Human_SNP_ID_808323602 m1A Human chr10 - 73874446 73874446 73874446 TCCGCCCGCCCGCCAGCATGGCCACCACCGCCACCTGCACCCGTTTCACCGACGACTACCAGCTC TCCGCCCGCCCGCCAGCATGGCCACCACCGCCGCCTGCACCCGTTTCACCGACGACTACCAGCTC T C CAMK2G Ensembl:ENSG00000148660 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:73874343..73874499;chr10:73874381..73874530 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 14 brain Human_RBP_ID_4136375 Human_Splice_Rec_1147695,Human_Splice_Rec_1147731,Human_Splice_Rec_1147771,Human_Splice_Rec_1147811,Human_Splice_Rec_1147851,Human_Splice_Rec_1147925,Human_Splice_Rec_1147965,Human_Splice_Rec_1148027 115580 RMVar_ID_115580 Human_SNP_ID_808323971 m1A Human chr10 - 104315879 104315876 104315879 GCTGCAGCTGGAGCAGTTGCGCCTGGAGGAGGAGGTGGCTCGGCTGGCGGCCGAAAAGGAGGCAC GCTGCAGCTGGAGCAGTTGCGCCTGGAGGAGG___TGGCTCGGCTGGCGGCCGAAAAGGAGGCAC ACCT A ITPRIP Ensembl:ENSG00000148841 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:104315776..104315970 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 COAD 1 - Human_RBP_ID_5137930,Human_RBP_ID_22029549 RMVar_hsa_circ_104371,RMVar_hsa_circ_146258,RMVar_hsa_circ_93051,RMVar_hsa_circ_146257 115581 RMVar_ID_115581 Human_SNP_ID_808353726 m1A Human chr10 + 35640597 35640597 35640597 AGCAGAGCACCGACCACAGGCCGATCCAGAAGACGGTGAAGGCGCGCTCGTCCTGGCTGAAAAAG AGCAGAGCACCGACCACAGGCCGATCCAGAAGTCGGTGAAGGCGCGCTCGTCCTGGCTGAAAAAG A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:35640547..35640771 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 1 skin,head and neck 115582 RMVar_ID_115582 Human_SNP_ID_808381075 m1A Human chr10 + 1000722 1000722 1000722 CTGGGATCCTGGACCACCCTCTGGAGGATAGGAACACCATCGAGATGCAGGCCATCACTGCCCTG CTGGGATCCTGGACCACCCTCTGGAGGATAGGTACACCATCGAGATGCAGGCCATCACTGCCCTG A T GTPBP4 Ensembl:ENSG00000107937 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:999068..1000850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_864521,Human_RBP_ID_1759249,Human_RBP_ID_3337197,Human_RBP_ID_3938117,Human_RBP_ID_8324738,Human_RBP_ID_9360057,Human_RBP_ID_11246800,Human_RBP_ID_18970551,Human_RBP_ID_22536516,Human_RBP_ID_26316016,Human_RBP_ID_26392191,Human_RBP_ID_27801819 Human_Splice_Rec_1106540,Human_Splice_Rec_1106566 RMVar_hsa_circ_58417,RMVar_hsa_circ_5835,RMVar_hsa_circ_302583,RMVar_hsa_circ_280435,RMVar_hsa_circ_107063,RMVar_hsa_circ_78785,RMVar_hsa_circ_141547,RMVar_hsa_circ_304483,RMVar_hsa_circ_141546,RMVar_hsa_circ_141550,RMVar_hsa_circ_141551,RMVar_hsa_circ_46618,RMVar_hsa_circ_375922,RMVar_hsa_circ_101346,RMVar_hsa_circ_7166,RMVar_hsa_circ_141552,RMVar_hsa_circ_22988,RMVar_hsa_circ_304700,RMVar_hsa_circ_323407,RMVar_hsa_circ_347750,RMVar_hsa_circ_319523,RMVar_hsa_circ_76810,RMVar_hsa_circ_329846,RMVar_hsa_circ_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553,RMVar_hsa_circ_337852,RMVar_hsa_circ_305285,RMVar_hsa_circ_307495,RMVar_hsa_circ_301685,RMVar_hsa_circ_141556,RMVar_hsa_circ_141558,RMVar_hsa_circ_141560,RMVar_hsa_circ_141561,RMVar_hsa_circ_141559,RMVar_hsa_circ_141557 115583 RMVar_ID_115583 Human_SNP_ID_808413211 m1A Human chr10 + 101040603 101040603 101040603 TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTAATGGAGTTTCACTATTTTGCCCAGGCTGGAGT TTTGTGTTCCATTGACTTTTTTTTTTTTTTTTGATGGAGTTTCACTATTTTGCCCAGGCTGGAGT A G SFXN3 Ensembl:ENSG00000107819 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs807048 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_11234440,Human_RBP_ID_24400980,Human_RBP_ID_24455933 Human_miRNA_ID_264208,Human_miRNA_ID_2047576 RMVar_hsa_circ_125598,RMVar_hsa_circ_145696,RMVar_hsa_circ_116236,RMVar_hsa_circ_145700 115584 RMVar_ID_115584 Human_SNP_ID_808429554 m1A Human chr10 - 102137914 102137914 102137914 TTAGCTCCTCCATTTCCAGGTCCTTGTCCCTCAGAGATGGGCCCAGCCGAGAGAGACTGACAAAG TTAGCTCCTCCATTTCCAGGTCCTTGTCCCTCTGAGATGGGCCCAGCCGAGAGAGACTGACAAAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:102133143..102138022 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 115585 RMVar_ID_115585 Human_SNP_ID_808433914 m1A Human chr10 - 1239355 1239354 1239356 AGGGGGGAGTAAACACCGGGAGGGAGAGGGGGAGTAAACACCGGGAGGCAGAGGGGAGTAAACAC AGGGGGGAGTAAACACCGGGAGGGAGAGGGG__GTAAACACCGGGAGGCAGAGGGGAGTAAACAC CTC C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1239296..1239403 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - RMVar_hsa_circ_16190,RMVar_hsa_circ_21433,RMVar_hsa_circ_312016 115586 RMVar_ID_115586 Human_SNP_ID_808437627 m1A Human chr10 + 13201468 13201468 13201468 CAGGAGCGCTACTTTGAGCCACTGGTGAAAAAAGAACAAATGGAAGAAAAGATGAGAAACATCAG CAGGAGCGCTACTTTGAGCCACTGGTGAAAAAGGAACAAATGGAAGAAAAGATGAGAAACATCAG A G MCM10 Ensembl:ENSG00000065328 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:13198804..13201567 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast metaplastic_carcinoma 3 breast Human_RBP_ID_3938178,Human_RBP_ID_23444507 Human_Splice_Rec_1113354,Human_Splice_Rec_1113355,Human_Splice_Rec_1113396,Human_Splice_Rec_1113397,Human_Splice_Rec_1113432,Human_Splice_Rec_1113433,Human_Splice_Rec_1113444,Human_Splice_Rec_1113446,Human_Splice_Rec_1113447 RMVar_hsa_circ_16709,RMVar_hsa_circ_1610,RMVar_hsa_circ_35190,RMVar_hsa_circ_142238,RMVar_hsa_circ_96426,RMVar_hsa_circ_38074,RMVar_hsa_circ_142239,RMVar_hsa_circ_351363,RMVar_hsa_circ_50635 115587 RMVar_ID_115587 Human_SNP_ID_808443265 m1A Human chr10 + 112951555 112951555 112951555 GTATCCCGGCTACCCCTTCATCATGATCCCCGACCTGACGAGCCCCTACCTCCCCAACGGATCGC GTATCCCGGCTACCCCTTCATCATGATCCCCGCCCTGACGAGCCCCTACCTCCCCAACGGATCGC A C TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:112951438..112951643 26863196 MeRIP-seq:(Medium) rs993289792 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_11263704,Human_RBP_ID_24782043 Human_Splice_Rec_1176796,Human_Splice_Rec_1176797,Human_Splice_Rec_1176822,Human_Splice_Rec_1176823,Human_Splice_Rec_1176842,Human_Splice_Rec_1176843,Human_Splice_Rec_1176868,Human_Splice_Rec_1176869,Human_Splice_Rec_1176892,Human_Splice_Rec_1176893,Human_Splice_Rec_1176920,Human_Splice_Rec_1176921,Human_Splice_Rec_1176948,Human_Splice_Rec_1176949,Human_Splice_Rec_1176974,Human_Splice_Rec_1176975,Human_Splice_Rec_1177000,Human_Splice_Rec_1177001,Human_Splice_Rec_1177024,Human_Splice_Rec_1177025,Human_Splice_Rec_1177052,Human_Splice_Rec_1177053,Human_Splice_Rec_1177080,Human_Splice_Rec_1177081,Human_Splice_Rec_1177108,Human_Splice_Rec_1177109,Human_Splice_Rec_1177132,Human_Splice_Rec_1177133 RMVar_hsa_circ_55138,RMVar_hsa_circ_51712 115588 RMVar_ID_115588 Human_SNP_ID_808451189 m1A Human chr10 - 5800703 5800703 5800703 TCTTTTCAAGGTACTATGCTTTTTCTATAGGAATGTATCCTGTCAGGTATAATGTCAGTGAATGG TCTTTTCAAGGTACTATGCTTTTTCTATAGGACTGTATCCTGTCAGGTATAATGTCAGTGAATGG T G GDI2 Ensembl:ENSG00000057608 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:5800654..5800733 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_22431370 Human_Splice_Rec_1108772,Human_Splice_Rec_1108806,Human_Splice_Rec_1108824,Human_Splice_Rec_1108842,Human_Splice_Rec_1108854,Human_Splice_Rec_1108864 Human_miRNA_ID_2362790,Human_miRNA_ID_2362791,Human_miRNA_ID_2439651 RMVar_hsa_circ_115518,RMVar_hsa_circ_106043,RMVar_hsa_circ_141772,RMVar_hsa_circ_141773,RMVar_hsa_circ_357087,RMVar_hsa_circ_141779,RMVar_hsa_circ_141782,RMVar_hsa_circ_141781,RMVar_hsa_circ_281208,RMVar_hsa_circ_271927,RMVar_hsa_circ_79431,RMVar_hsa_circ_141785,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_141788,RMVar_hsa_circ_277849,RMVar_hsa_circ_270373,RMVar_hsa_circ_268769,RMVar_hsa_circ_141790,RMVar_hsa_circ_141789,RMVar_hsa_circ_141793,RMVar_hsa_circ_288869,RMVar_hsa_circ_362230,RMVar_hsa_circ_276627,RMVar_hsa_circ_120617,RMVar_hsa_circ_276313,RMVar_hsa_circ_141794,RMVar_hsa_circ_141795,RMVar_hsa_circ_141796 115589 RMVar_ID_115589 Human_SNP_ID_808476089 m1A Human chr10 + 124498165 124498165 124498165 GTTGGCGCCTTGTGAAGTGGGTCAGGGGAGGCAGCCCCGTCAGGGAGGCCCTGGAGCTTGGAATG GTTGGCGCCTTGTGAAGTGGGTCAGGGGAGGCCGCCCCGTCAGGGAGGCCCTGGAGCTTGGAATG A C LHPP Ensembl:ENSG00000107902 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:124498161..124498237 26863196 MeRIP-seq:(Medium) rs3832703 Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 3 stomach Human_RBP_ID_5234651 RMVar_hsa_circ_146938,RMVar_hsa_circ_317789,RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_332404,RMVar_hsa_circ_146942,RMVar_hsa_circ_288010,RMVar_hsa_circ_86169,RMVar_hsa_circ_146945,RMVar_hsa_circ_146946 115590 RMVar_ID_115590 Human_SNP_ID_808520101 m1A Human chr10 - 73247202 73247202 73247202 CAGCTGGGAGCGGCTGCTTCCTCCGGGGTCGTATCTCCGCCCGGCATGGGGCTGCTGGACCTTTG CAGCTGGGAGCGGCTGCTTCCTCCGGGGTCGTCTCTCCGCCCGGCATGGGGCTGCTGGACCTTTG T G DNAJC9 Ensembl:ENSG00000213551 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:73246971..73247275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_RBP_ID_4135889,Human_RBP_ID_5273581,Human_RBP_ID_5998297,Human_RBP_ID_8762987,Human_RBP_ID_8940378,Human_RBP_ID_9320604,Human_RBP_ID_11422789,Human_RBP_ID_18416274,Human_RBP_ID_18970031,Human_RBP_ID_22030088,Human_RBP_ID_24831837,Human_RBP_ID_27194924 115591 RMVar_ID_115591 Human_SNP_ID_808532064 m1A Human chr10 - 128104715 128104715 128104715 AGGAAAGCAGACGTAGAGGAAGAATTTTTAGCACTCAGGAAACGAACACCATCAGCAGGCAAAGC AGGAAAGCAGACGTAGAGGAAGAATTTTTAGCGCTCAGGAAACGAACACCATCAGCAGGCAAAGC T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:128104664..128104822 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_2320,Human_RBP_ID_27558,Human_RBP_ID_1443760,Human_RBP_ID_1762982,Human_RBP_ID_2198348,Human_RBP_ID_8759306,Human_RBP_ID_9360983,Human_RBP_ID_11308598,Human_RBP_ID_26316834,Human_RBP_ID_27802445 Human_miRNA_ID_1092394 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 115592 RMVar_ID_115592 Human_SNP_ID_808548104 m1A Human chr10 + 12889046 12889038 12889047 ACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGATAGATAGATAGATAGACAGA ACGGACGGACGGACGGACGGACGGA_________AGATAGATAGATAGATAGATAGATAGACAGA ACGGACAGAT A AL353586.1 Ensembl:ENSG00000285520 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:12888992..12889112 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 26..34 33 SKCA 1 - 115593 RMVar_ID_115593 Human_SNP_ID_808587616 m1A Human chr10 - 27180967 27180967 27180967 AAATTCAAACAAGCAAACTCCAAGTGCCCACCAGTCTACCGCAGGACCTGTAATCGAAGAGGAAA AAATTCAAACAAGCAAACTCCAAGTGCCCACCGGTCTACCGCAGGACCTGTAATCGAAGAGGAAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27173125..27180968 32194978 MeRIP-seq:(Medium) rs757596656 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 115594 RMVar_ID_115594 Human_SNP_ID_808602851 m1A Human chr10 - 93496760 93496760 93496760 TGCCCACTGACCTGCCCTCCCTGGCGGTCCGGACCGGCCCGGCCCCGGGGCTGCGGGTCCTGGCC TGCCCACTGACCTGCCCTCCCTGGCGGTCCGGCCCGGCCCGGCCCCGGGGCTGCGGGTCCTGGCC T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:93496659..93496800 26863196 MeRIP-seq:(Medium) rs1000112075 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115595 RMVar_ID_115595 Human_SNP_ID_808610697 m1A Human chr10 + 102365521 102365521 102365521 CAACACAGAGGTTGCTCAGTGGCTCCGAGAGAACCCTCGGCTGGACAAGAAGATGATTGGAGAGT CAACACAGAGGTTGCTCAGTGGCTCCGAGAGACCCCTCGGCTGGACAAGAAGATGATTGGAGAGT A C GBF1 Ensembl:ENSG00000107862 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102365399..102365600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11243815,Human_RBP_ID_23430662,Human_RBP_ID_27802970 Human_Splice_Rec_1171051,Human_Splice_Rec_1171131,Human_Splice_Rec_1171209 RMVar_hsa_circ_93134,RMVar_hsa_circ_145909,RMVar_hsa_circ_265907,RMVar_hsa_circ_66484,RMVar_hsa_circ_145913,RMVar_hsa_circ_81558,RMVar_hsa_circ_109294,RMVar_hsa_circ_145914,RMVar_hsa_circ_113836,RMVar_hsa_circ_322644,RMVar_hsa_circ_272261,RMVar_hsa_circ_97598,RMVar_hsa_circ_27695,RMVar_hsa_circ_18302,RMVar_hsa_circ_4157,RMVar_hsa_circ_100359,RMVar_hsa_circ_145916,RMVar_hsa_circ_145917,RMVar_hsa_circ_145918,RMVar_hsa_circ_364035,RMVar_hsa_circ_145923,RMVar_hsa_circ_54698,RMVar_hsa_circ_290739,RMVar_hsa_circ_145921,RMVar_hsa_circ_281314,RMVar_hsa_circ_12751,RMVar_hsa_circ_145922,RMVar_hsa_circ_377879,RMVar_hsa_circ_91871,RMVar_hsa_circ_101493,RMVar_hsa_circ_22543,RMVar_hsa_circ_145926,RMVar_hsa_circ_145927 115596 RMVar_ID_115596 Human_SNP_ID_808615512 m1A Human chr10 - 128103225 128103225 128103225 CACACAAACCTCAGGGGAGACCACGCACACCGACAAAGAGCCGGTAGGTGAGGGCAAAGGCACGA CACACAAACCTCAGGGGAGACCACGCACACCGTCAAAGAGCCGGTAGGTGAGGGCAAAGGCACGA T A MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr10:128103176..128103250;chr10:128103175..128103275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_1443726,Human_RBP_ID_2198310,Human_RBP_ID_9360973,Human_RBP_ID_18158859,Human_RBP_ID_18410354,Human_RBP_ID_22879224,Human_RBP_ID_24542059,Human_RBP_ID_26316003 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 115597 RMVar_ID_115597 Human_SNP_ID_808654644 m1A Human chr10 + 73772393 73772393 73772393 TTGGTCCTTCTAGGGGTGCTCAGTGTCTGTGCAGCCAGCGGCCATGGGTCCGTAGCGGAGAGGGA TTGGTCCTTCTAGGGGTGCTCAGTGTCTGTGCGGCCAGCGGCCATGGGTCCGTAGCGGAGAGGGA A G FUT11 Ensembl:ENSG00000196968 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:73772342..73772552 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_4135893,Human_RBP_ID_8765659 115598 RMVar_ID_115598 Human_SNP_ID_808691089 m1A Human chr10 + 77821737 77821737 77821737 CACAGGGGCCCACCTCGGTCTCAAAGGGCAGCAGTGGCCGCCGGCCACGCACGTCCACCAGCCCA CACAGGGGCCCACCTCGGTCTCAAAGGGCAGCGGTGGCCGCCGGCCACGCACGTCCACCAGCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:77821688..77821789 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115599 RMVar_ID_115599 Human_SNP_ID_808720923 m1A Human chr10 + 68989008 68989008 68989008 GCTGCTCGGCCCTGCGCCTGAGGACGAGGATGAGCGGCCTGAGGCCGAGGACGGCCCGGGTGCCG GCTGCTCGGCCCTGCGCCTGAGGACGAGGATGGGCGGCCTGAGGCCGAGGACGGCCCGGGTGCCG A G KIFBP Ensembl:ENSG00000198954 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:68988826..68989081 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_22432025 115600 RMVar_ID_115600 Human_SNP_ID_808733347 m1A Human chr10 - 128108733 128108733 128108733 GAAGGCATCCCTGGGGAAAGTAGGTGTGAAAGAAGAGCTCCTAGCAGTCGGCAAGTTCACACGGA GAAGGCATCCCTGGGGAAAGTAGGTGTGAAAGGAGAGCTCCTAGCAGTCGGCAAGTTCACACGGA T C MKI67 Ensembl:ENSG00000148773 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:128108683..128108861 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_27582,Human_RBP_ID_1443837,Human_RBP_ID_1763032,Human_RBP_ID_3343689,Human_RBP_ID_4112691,Human_RBP_ID_5946319,Human_RBP_ID_8759425,Human_RBP_ID_9361000,Human_RBP_ID_18590151,Human_RBP_ID_22029623,Human_RBP_ID_23443827,Human_RBP_ID_24542073,Human_RBP_ID_26316861 Human_miRNA_ID_2292077,Human_miRNA_ID_2357420,Human_miRNA_ID_3059862 RMVar_hsa_circ_77374,RMVar_hsa_circ_128148,RMVar_hsa_circ_94413,RMVar_hsa_circ_90595,RMVar_hsa_circ_147193,RMVar_hsa_circ_147194,RMVar_hsa_circ_147192,RMVar_hsa_circ_65772,RMVar_hsa_circ_147197,RMVar_hsa_circ_61287 115601 RMVar_ID_115601 Human_SNP_ID_808736103 m1A Human chr10 + 100987416 100987416 100987416 ACCCAGTCCGTTGTGGAGAACGCTGGCCAAGAAGCGGCTCGGAGTCCCGCGCGCCGTCATAGCTA ACCCAGTCCGTTGTGGAGAACGCTGGCCAAGAGGCGGCTCGGAGTCCCGCGCGCCGTCATAGCTA A G TWNK Ensembl:ENSG00000107815 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:100987365..100987475 26863196 MeRIP-seq:(Medium) rs1294828350 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 115602 RMVar_ID_115602 Human_SNP_ID_808789748 m1A Human chr10 + 31319290 31319290 31319290 GCGCAGAAAGCAGGCGAACCCGCGGCGCAATAACGGTGAGTGGCGGAGGGGACCGGGGAGCGGCG GCGCAGAAAGCAGGCGAACCCGCGGCGCAATAGCGGTGAGTGGCGGAGGGGACCGGGGAGCGGCG A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:31319240..31319441 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung Human_RBP_ID_5339853,Human_RBP_ID_19046324 Human_Splice_Rec_1123029,Human_Splice_Rec_1123045,Human_Splice_Rec_1123061,Human_Splice_Rec_1123077,Human_Splice_Rec_1123091,Human_Splice_Rec_1123099,Human_Splice_Rec_1123111,Human_Splice_Rec_1123131 RMVar_hsa_circ_86288,RMVar_hsa_circ_101171,RMVar_hsa_circ_142926,RMVar_hsa_circ_142927 115603 RMVar_ID_115603 Human_SNP_ID_808810727 m1A Human chr10 - 5937143 5937143 5937143 GGGCCCGATGCGCTGCTCCGCACAGGAGTGGCAGAGGTAGCCCCCCTTGTTTTCCTTCCTGTTGC GGGCCCGATGCGCTGCTCCGCACAGGAGTGGCGGAGGTAGCCCCCCTTGTTTTCCTTCCTGTTGC T C AL137186.2 Ensembl:ENSG00000232807 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:5936472..5937146 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 115604 RMVar_ID_115604 Human_SNP_ID_808832652 m1A Human chr10 + 27504377 27504377 27504377 GGGCTCGGAGCGGAACGGGGTCAGGATGGACGAGGACGTGCTAACCACCCTGAAGATCCTCATCA GGGCTCGGAGCGGAACGGGGTCAGGATGGACGGGGACGTGCTAACCACCCTGAAGATCCTCATCA A G RAB18 Ensembl:ENSG00000099246 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:27504326..27504446 26863196 MeRIP-seq:(Medium) rs1315455064 Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_1445589,Human_RBP_ID_4116581,Human_RBP_ID_5959465,Human_RBP_ID_8760360,Human_RBP_ID_18970683,Human_RBP_ID_22886605,Human_RBP_ID_27801954 Human_Splice_Rec_1121109,Human_Splice_Rec_1121117,Human_Splice_Rec_1121125,Human_Splice_Rec_1121137,Human_Splice_Rec_1121145,Human_Splice_Rec_1121159,Human_Splice_Rec_1121169 RMVar_hsa_circ_110698,RMVar_hsa_circ_142848 115605 RMVar_ID_115605 Human_SNP_ID_808855901 m1A Human chr10 + 72274758 72274758 72274758 CGACTTCGAGCTGCTCAGTGACCCTGAGGATGAACACTTGTGTGCCAACCTGATGCAGCTGCTGC CGACTTCGAGCTGCTCAGTGACCCTGAGGATGGACACTTGTGTGCCAACCTGATGCAGCTGCTGC A G DDIT4 Ensembl:ENSG00000168209 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_1159747,Human_RBP_ID_1449542,Human_RBP_ID_4135883,Human_RBP_ID_5996035,Human_RBP_ID_8991888,Human_RBP_ID_11416993,Human_RBP_ID_18970796,Human_RBP_ID_22431464,Human_RBP_ID_22567638,Human_RBP_ID_22886636,Human_RBP_ID_23467582,Human_RBP_ID_27194810,Human_RBP_ID_27406977 Human_Splice_Rec_1144978,Human_Splice_Rec_1144980 Human_miRNA_ID_1986600,Human_miRNA_ID_3123123 RMVar_hsa_circ_88567,RMVar_hsa_circ_98073,RMVar_hsa_circ_144178,RMVar_hsa_circ_144179 115606 RMVar_ID_115606 Human_SNP_ID_808899392 m1A Human chr10 - 131919020 131919016 131919020 CTGTGTCATCCCGCTCGCCTGAGGTCCCTACAAACACTGTGTCATTCCACCCGCCTGAGGTCCCT CTGTGTCATCCCGCTCGCCTGAGGTCCCTACA____CTGTGTCATTCCACCCGCCTGAGGTCCCT GTGTT G lnc-BNIP3-1,lnc-BNIP3-1:2 RNACentral:URS00009BEB97,RNACentral:URS00008B94C7 lincRNA,lincRNA exon,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:131919009..131919101 26863196 MeRIP-seq:(Medium) rs1311151013 Functional Loss DEL ICGC 33..36 33 PEME 1 - 115607 RMVar_ID_115607 Human_SNP_ID_808900620 m1A Human chr10 - 24621023 24621023 24621023 GGTTGTAGATTTGTTATCCAATAGAAACAACCATACAGGTCCTTCACATAGAACTGAAGAAGTGA GGTTGTAGATTTGTTATCCAATAGAAACAACCGTACAGGTCCTTCACATAGAACTGAAGAAGTGA T C ARHGAP21 Ensembl:ENSG00000107863 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:24620972..24621075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 5 oesophagus Human_RBP_ID_1764499,Human_RBP_ID_17774938,Human_RBP_ID_26801857 Human_miRNA_ID_2472781,Human_miRNA_ID_2923663 RMVar_hsa_circ_2959,RMVar_hsa_circ_33618,RMVar_hsa_circ_265491,RMVar_hsa_circ_51350,RMVar_hsa_circ_70420,RMVar_hsa_circ_83594,RMVar_hsa_circ_142675,RMVar_hsa_circ_142678,RMVar_hsa_circ_289615,RMVar_hsa_circ_303181,RMVar_hsa_circ_347323,RMVar_hsa_circ_323058,RMVar_hsa_circ_290657,RMVar_hsa_circ_142680,RMVar_hsa_circ_275238,RMVar_hsa_circ_142679,RMVar_hsa_circ_142677 115608 RMVar_ID_115608 Human_SNP_ID_808935481 m1A Human chr10 - 77926360 77926360 77926360 GCTGGACGAGGAGGCGGGAGGCGCCAAGGCGGAGCTGCTGCTCAAGCTGCTCTTGGCCAAGGAGC GCTGGACGAGGAGGCGGGAGGCGCCAAGGCGGTGCTGCTGCTCAAGCTGCTCTTGGCCAAGGAGC T A DLG5 Ensembl:ENSG00000151208 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:77926313..77926720 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_748143,Human_RBP_ID_9320944 115609 RMVar_ID_115609 Human_SNP_ID_808963040 m1A Human chr10 + 77927068 77927068 77927068 CCGGCCCGGCTCACCGGGGCCCCGCGGCCGCCACCCGCTCCCCCGTGGCCACAGCCCCGCCGCCG CCGGCCCGGCTCACCGGGGCCCCGCGGCCGCCCCCCGCTCCCCCGTGGCCACAGCCCCGCCGCCG A C DLG5-AS1,DLG5-AS1:2,DLG5-AS1:3,DLG5-AS1:4,lnc-RPS24-14 RNACentral:URS0000759D71,RNACentral:URS00009C43DB,RNACentral:URS00008B899B,RNACentral:URS00008B9497,RNACentral:URS00008B3393 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:77926784..77927103 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - 115610 RMVar_ID_115610 Human_SNP_ID_808968287 m1A Human chr10 + 32015584 32015584 32015584 CTCGCACTGCCACTGGCTGGCTGTTCTGAACAAATGCACCTCCTCCACGAATTGCACTTGGGTGA CTCGCACTGCCACTGGCTGGCTGTTCTGAACACATGCACCTCCTCCACGAATTGCACTTGGGTGA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:32011449..32017174 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney RMVar_hsa_circ_93747,RMVar_hsa_circ_142980 115611 RMVar_ID_115611 Human_SNP_ID_809011561 m1A Human chr10 + 113165821 113165821 113165821 GGCCACCCACAAGGCCTCCGCCCTCTGTCCCAACGGGGCCCTGGACCTGCCCCCAGCCGCTTTGC GGCCACCCACAAGGCCTCCGCCCTCTGTCCCAGCGGGGCCCTGGACCTGCCCCCAGCCGCTTTGC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr10:113165801..113165825 26863196 MeRIP-seq:(Medium) rs762832310 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 11 brain Human_RBP_ID_18931919 115612 RMVar_ID_115612 Human_SNP_ID_809047057 m1A Human chr10 + 15860425 15860423 15860426 GGCGGCAAACGAATTGGAAGGTGAGGCAGGAAAGAAGAAGGGGCTGAGAGCCACTTGCAGAGACC GGCGGCAAACGAATTGGAAGGTGAGGCAGGA___AAGAAGGGGCTGAGAGCCACTTGCAGAGACC AAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:15860378..15860465 26863196 MeRIP-seq:(Medium) rs1439956176 Functional Loss DEL ICGC 32..34 33 STAD 1 - 115613 RMVar_ID_115613 Human_SNP_ID_809052671 m1A Human chr10 - 5800669 5800669 5800669 GTATCCTGTCAGGTATAATGTCAGTGAATGGCAAGAAAGTTCTTCATATGGATCGAAACCCTTAC GTATCCTGTCAGGTATAATGTCAGTGAATGGCTAGAAAGTTCTTCATATGGATCGAAACCCTTAC T A GDI2 Ensembl:ENSG00000057608 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:5796777..5813386 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_378839,Human_RBP_ID_1447569,Human_RBP_ID_1767754,Human_RBP_ID_22432332,Human_RBP_ID_23460366,Human_RBP_ID_26879967 Human_Splice_Rec_1108772,Human_Splice_Rec_1108773,Human_Splice_Rec_1108806,Human_Splice_Rec_1108807,Human_Splice_Rec_1108824,Human_Splice_Rec_1108825,Human_Splice_Rec_1108842,Human_Splice_Rec_1108843,Human_Splice_Rec_1108854,Human_Splice_Rec_1108855,Human_Splice_Rec_1108864,Human_Splice_Rec_1108865 RMVar_hsa_circ_115518,RMVar_hsa_circ_106043,RMVar_hsa_circ_141772,RMVar_hsa_circ_141773,RMVar_hsa_circ_357087,RMVar_hsa_circ_141779,RMVar_hsa_circ_141782,RMVar_hsa_circ_141781,RMVar_hsa_circ_281208,RMVar_hsa_circ_271927,RMVar_hsa_circ_79431,RMVar_hsa_circ_141785,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_141788,RMVar_hsa_circ_277849,RMVar_hsa_circ_270373,RMVar_hsa_circ_268769,RMVar_hsa_circ_141790,RMVar_hsa_circ_141789,RMVar_hsa_circ_141793,RMVar_hsa_circ_288869,RMVar_hsa_circ_362230,RMVar_hsa_circ_276627,RMVar_hsa_circ_120617,RMVar_hsa_circ_276313,RMVar_hsa_circ_141794,RMVar_hsa_circ_141795,RMVar_hsa_circ_141796 115614 RMVar_ID_115614 Human_SNP_ID_809052778 m1A Human chr10 + 97640760 97640760 97640760 CCGGCTGTCTGAGGGATGGACGAGACGAGCCCACTAGTGTCCCCCGAGCGGGCCCAACCCCCGGA CCGGCTGTCTGAGGGATGGACGAGACGAGCCCCCTAGTGTCCCCCGAGCGGGCCCAACCCCCGGA A C PI4K2A,AL355315.1 Ensembl:ENSG00000155252,Ensembl:ENSG00000249967 Protein coding,Protein coding CDS,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:97640713..97640885 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 115615 RMVar_ID_115615 Human_SNP_ID_809055439 m1A Human chr10 - 119672360 119672360 119672360 GTTCTGCTCGTGTATCACCGGAATGGAGATGTACCCCCGCGGGAGCTGGTGACTGCCCAGGCTGC GTTCTGCTCGTGTATCACCGGAATGGAGATGTGCCCCCGCGGGAGCTGGTGACTGCCCAGGCTGC T C lnc-TIAL1-1,lnc-TIAL1-1:2,lnc-TIAL1-1:3,lnc-TIAL1-1:4 RNACentral:URS0000D5A908,RNACentral:URS00008C3BF0,RNACentral:URS0000D5973A,RNACentral:URS00009B8A32 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:119672310..119672591 26863196 MeRIP-seq:(Medium) rs755456690 Functional Loss SNV ICGC 33..33 33 MALY 1 - 115616 RMVar_ID_115616 Human_SNP_ID_809055606 m1A Human chr10 - 124461894 124461869 124461895 GCACGCCCGAGATGTCAAGCAGCACCCCGCGCACGCCAGCCAGCCGCTTGCCCCACGGTGCCATG GCACGCCCGAGATGTCAAGCAGCACCCCGCG__________________________GTGCCATG CCGTGGGGCAAGCGGCTGGCTGGCGTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:124461851..124462040 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..57 33 PAAD 1 - 115617 RMVar_ID_115617 Human_SNP_ID_809112190 m1A Human chr10 - 14878942 14878942 14878942 CCTTGGGAGCTTGCCTGGGAACAGGGAAGGCGAGGGGGCCGCGCTCCAGCCTCACCTCCTCGCGC CCTTGGGAGCTTGCCTGGGAACAGGGAAGGCGGGGGGGCCGCGCTCCAGCCTCACCTCCTCGCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:14878935..14879038 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115618 RMVar_ID_115618 Human_SNP_ID_809134478 m1A Human chr10 - 3785067 3785044 3785068 GCGCTCCGGGGAGACTTTCGGCTCCGGCTCCCACCGCGCGCCTCGCCGCCCTCGCGACCGCGGGC GCGCTCCGGGGAGACTTTCGGCTCCGGCTCC________________________GACCGCGGGC CGCGAGGGCGGCGAGGCGCGCGGTG C KLF6 Ensembl:ENSG00000067082 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:3785023..3785094 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..55 33 KIRP 1 - Human_RBP_ID_747030,Human_RBP_ID_4135747,Human_RBP_ID_17345564,Human_RBP_ID_22029145 RMVar_hsa_circ_81579,RMVar_hsa_circ_141683 115619 RMVar_ID_115619 Human_SNP_ID_809177330 m1A Human chr10 - 97714220 97714220 97714220 AGTAGCTGTGGCGCTGCATCTGGTCGCTCATGATGCCGGTGGCGGCGCCGTAGAGCGCGGCCGCC AGTAGCTGTGGCGCTGCATCTGGTCGCTCATGGTGCCGGTGGCGGCGCCGTAGAGCGCGGCCGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:97714170..97714320 26863196 MeRIP-seq:(Medium) rs1419687206 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 115620 RMVar_ID_115620 Human_SNP_ID_809179780 m1A Human chr10 - 129546322 129546322 129546322 TCAGCCCCATTCAGCTCTGTGGCCAGTCACCTAGGCTTGGGCCCCTGCCAGCCGCTGTCTTGAGG TCAGCCCCATTCAGCTCTGTGGCCAGTCACCTGGGCTTGGGCCCCTGCCAGCCGCTGTCTTGAGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:129546309..129546392 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 115621 RMVar_ID_115621 Human_SNP_ID_809185812 m1A Human chr10 - 103637983 103637983 103637983 TCTGACCAGGGGAGGCCTGGCCGAGGGTGGGCAGCCTTTCACTGGTCTTAAAGGCACAGCACTCG TCTGACCAGGGGAGGCCTGGCCGAGGGTGGGCGGCCTTTCACTGGTCTTAAAGGCACAGCACTCG T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:103637979..103638092 26863196 MeRIP-seq:(Medium) rs7910092 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_3364900 RMVar_hsa_circ_35758,RMVar_hsa_circ_324517,RMVar_hsa_circ_291291,RMVar_hsa_circ_71694,RMVar_hsa_circ_344284,RMVar_hsa_circ_290916,RMVar_hsa_circ_19664,RMVar_hsa_circ_310670 115622 RMVar_ID_115622 Human_SNP_ID_809188055 m1A Human chr10 - 77821695 77821695 77821695 TGAGACCGAGGTGGGCCCCTGTGGGGTTGGGGAGGCCTCCCTGGACAAGGCAGACTCTGAAGGCT TGAGACCGAGGTGGGCCCCTGTGGGGTTGGGGGGGCCTCCCTGGACAAGGCAGACTCTGAAGGCT T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:77821651..77821800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_105345,Human_RBP_ID_3937878,Human_RBP_ID_5234856,Human_RBP_ID_5520152,Human_RBP_ID_8765680,Human_RBP_ID_18432054 RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_126566,RMVar_hsa_circ_144521,RMVar_hsa_circ_99757,RMVar_hsa_circ_94488,RMVar_hsa_circ_144522,RMVar_hsa_circ_144523,RMVar_hsa_circ_111944,RMVar_hsa_circ_144524,RMVar_hsa_circ_144526,RMVar_hsa_circ_77664,RMVar_hsa_circ_144525,RMVar_hsa_circ_101502,RMVar_hsa_circ_105290,RMVar_hsa_circ_144527,RMVar_hsa_circ_144528 115623 RMVar_ID_115623 Human_SNP_ID_809189554 m1A Human chr10 + 60778631 60778631 60778631 TAGGGGACGGCCGAGGGCCTCGGAGGGCGAGTATTGAGGAACGGGGTCCTCTAAGAAGGCCGGAC TAGGGGACGGCCGAGGGCCTCGGAGGGCGAGTGTTGAGGAACGGGGTCCTCTAAGAAGGCCGGAC A G CDK1 Ensembl:ENSG00000170312 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr10:60778571..60778708 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus Human_RBP_ID_4122588,Human_RBP_ID_5339169,Human_RBP_ID_5983171,Human_RBP_ID_9320561,Human_RBP_ID_19045362,Human_RBP_ID_27836013 Human_Splice_Rec_1137135 115624 RMVar_ID_115624 Human_SNP_ID_809207896 m1A Human chr10 - 56357908 56357908 56357908 AGGGGGTACTGGCCTTGGGCCTCCTATGATGCAGACATGGTGAATTTAATTCAAGGAGGAGGAGA AGGGGGTACTGGCCTTGGGCCTCCTATGATGCTGACATGGTGAATTTAATTCAAGGAGGAGGAGA T A ZWINT Ensembl:ENSG00000122952 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:56357859..56358043;chr10:56357857..56357963 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_378783,Human_RBP_ID_4121739,Human_RBP_ID_17778911,Human_RBP_ID_22882531,Human_RBP_ID_23460285 Human_miRNA_ID_1008426,Human_miRNA_ID_2979202 RMVar_hsa_circ_86937,RMVar_hsa_circ_125952,RMVar_hsa_circ_143481,RMVar_hsa_circ_143482 115625 RMVar_ID_115625 Human_SNP_ID_809220689 m1A Human chr10 - 124403026 124403026 124403026 TAGGTTCTCTTTATTGCTGATGAAATACAGACAGGATTGGCCAGAACTGGTAGATGGCTGGCTGT TAGGTTCTCTTTATTGCTGATGAAATACAGACGGGATTGGCCAGAACTGGTAGATGGCTGGCTGT T C OAT Ensembl:ENSG00000065154 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:124402976..124403113 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_373115,Human_RBP_ID_1443246,Human_RBP_ID_1762397,Human_RBP_ID_5942852,Human_RBP_ID_8758925,Human_RBP_ID_8984767,Human_RBP_ID_9274033,Human_RBP_ID_11296938,Human_RBP_ID_22431623,Human_RBP_ID_22639718,Human_RBP_ID_27604676 Human_Splice_Rec_1186320,Human_Splice_Rec_1186321,Human_Splice_Rec_1186336,Human_Splice_Rec_1186337,Human_Splice_Rec_1186343,Human_Splice_Rec_1186358,Human_Splice_Rec_1186359 RMVar_hsa_circ_61446,RMVar_hsa_circ_302216,RMVar_hsa_circ_269280,RMVar_hsa_circ_146933,RMVar_hsa_circ_325845,RMVar_hsa_circ_344537,RMVar_hsa_circ_351734 115626 RMVar_ID_115626 Human_SNP_ID_809250822 m1A Human chr10 - 21173868 21173868 21173868 GGGGGATGTCACAGCGGCTCCTGGGAGCCAGCAGCCGCCGCCGCCGCCGCCCCCGGGAACCGCGA GGGGGATGTCACAGCGGCTCCTGGGAGCCAGCCGCCGCCGCCGCCGCCGCCCCCGGGAACCGCGA T G NEBL Ensembl:ENSG00000078114 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA heat shock 4h chr10:21173844..21173970;chr10:21173828..21173981 26863196 MeRIP-seq:(Medium) rs552261723 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_4140835 115627 RMVar_ID_115627 Human_SNP_ID_809253402 m1A Human chr10 + 27155542 27155542 27155542 ACCGCCCTCCATTGAGGAATTCAGCATAGTGAAGCCCATTAGCCGGGGCGCCTTCGGGAAAGTGT ACCGCCCTCCATTGAGGAATTCAGCATAGTGAGGCCCATTAGCCGGGGCGCCTTCGGGAAAGTGT A G MASTL Ensembl:ENSG00000120539 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27155376..27165101 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_376109,Human_RBP_ID_4116427,Human_RBP_ID_23451363 Human_Splice_Rec_1120821,Human_Splice_Rec_1120843,Human_Splice_Rec_1120865 115628 RMVar_ID_115628 Human_SNP_ID_809254104 m1A Human chr10 - 102117560 102117560 102117560 GAAGGGGGGCAGGCACACTGGAGGCCTGGGTCAGGGAGCCCCAGGGGCCCGGGCAGGGGGCAGTG GAAGGGGGGCAGGCACACTGGAGGCCTGGGTCGGGGAGCCCCAGGGGCCCGGGCAGGGGGCAGTG T C LDB1 Ensembl:ENSG00000198728 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:102117557..102117696 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 115629 RMVar_ID_115629 Human_SNP_ID_809260531 m1A Human chr10 + 27122945 27122945 27122945 CCACCAACAGAATCTAATTCATCAATAAATATAACACAAGGAGCATTCGCCTTTGCTTCCCCTAA CCACCAACAGAATCTAATTCATCAATAAATATGACACAAGGAGCATTCGCCTTTGCTTCCCCTAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:27122853..27126722 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115630 RMVar_ID_115630 Human_SNP_ID_809295065 m1A Human chr10 + 43396513 43396513 43396513 TGTTGCTACCAGGCAAGCGCGGCTGGCAGCCAAGAGCCCCGAAATTCCACCGAAGCTCAACCACG TGTTGCTACCAGGCAAGCGCGGCTGGCAGCCAGGAGCCCCGAAATTCCACCGAAGCTCAACCACG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:43396451..43396525 26863196 MeRIP-seq:(Medium) rs1034361239 Functional Loss SNV ICGC 33..33 33 RECA 1 - 115631 RMVar_ID_115631 Human_SNP_ID_809325223 m1A Human chr10 + 75028952 75028952 75028952 GAAGAGGAAGGGGAAGAAGAAGAAGGAGGAGGAAATGTAGAAAAAGATCCAGATGGTGCTAAAAG GAAGAGGAAGGGGAAGAAGAAGAAGGAGGAGGGAATGTAGAAAAAGATCCAGATGGTGCTAAAAG A G KAT6B Ensembl:ENSG00000156650 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:75028829..75029150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_18432040,Human_RBP_ID_24542111 115632 RMVar_ID_115632 Human_SNP_ID_809434532 m1A Human chr10 - 3116853 3116853 3116853 CCTTAAAAGCAGGTCATAGAGTTGAGATTTGGAAGTTACCGTTTTGTCCCAAGAATGGAGCCTCC CCTTAAAAGCAGGTCATAGAGTTGAGATTTGGGAGTTACCGTTTTGTCCCAAGAATGGAGCCTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:3116851..3116875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain 115633 RMVar_ID_115633 Human_SNP_ID_809474788 m1A Human chr10 + 102230714 102230714 102230714 CGCGGCGGCGGCGGCGGCCGAGGCATAAGGGCAGGACACGGCCCCGGAGGACACGGCGGCCGGAG CGCGGCGGCGGCGGCGGCCGAGGCATAAGGGCGGGACACGGCCCCGGAGGACACGGCGGCCGGAG A G lnc-ELOVL3-1 RNACentral:URS00008BDF5B lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr10:102230665..102230904 26863196 MeRIP-seq:(Medium) rs1408808489 Functional Loss SNV ICGC 33..33 33 STAD 1 - 115634 RMVar_ID_115634 Human_SNP_ID_809496745 m1A Human chr10 + 69368620 69368619 69368620 CAGATGTGGTCAAACTGCTTAACAAAGCCATCAAAAAGCGAGGGGTAATTTCTCCTGGGCCCTCT CAGATGTGGTCAAACTGCTTAACAAAGCCATC_AAAAGCGAGGGGTAATTTCTCCTGGGCCCTCT CA C HK1 Ensembl:ENSG00000156515 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_18596945,Human_RBP_ID_26316390,Human_RBP_ID_26801973 Human_Splice_Rec_1140628,Human_Splice_Rec_1140629,Human_Splice_Rec_1140686,Human_Splice_Rec_1140687,Human_Splice_Rec_1140728,Human_Splice_Rec_1140729,Human_Splice_Rec_1140812,Human_Splice_Rec_1140813,Human_Splice_Rec_1140874,Human_Splice_Rec_1140875,Human_Splice_Rec_1140908,Human_Splice_Rec_1140909,Human_Splice_Rec_1140942,Human_Splice_Rec_1140943,Human_Splice_Rec_1140974,Human_Splice_Rec_1140975 RMVar_hsa_circ_27375,RMVar_hsa_circ_5647,RMVar_hsa_circ_54196,RMVar_hsa_circ_12746,RMVar_hsa_circ_30319,RMVar_hsa_circ_57635,RMVar_hsa_circ_116921,RMVar_hsa_circ_307242,RMVar_hsa_circ_47729,RMVar_hsa_circ_144006,RMVar_hsa_circ_144008,RMVar_hsa_circ_144007,RMVar_hsa_circ_274408,RMVar_hsa_circ_366153,RMVar_hsa_circ_97069,RMVar_hsa_circ_120740,RMVar_hsa_circ_144011,RMVar_hsa_circ_144010,RMVar_hsa_circ_98960,RMVar_hsa_circ_144012,RMVar_hsa_circ_144013 115635 RMVar_ID_115635 Human_SNP_ID_809517456 m1A Human chr10 + 68771352 68771352 68771352 AAAAGCAAAAAAGATGAGAGAAAAGATAAAAAAGAAGAAAGAGATGATGAAACTGATGAACCAAA AAAAGCAAAAAAGATGAGAGAAAAGATAAAAATGAAGAAAGAGATGATGAAACTGATGAACCAAA A T CCAR1 Ensembl:ENSG00000060339 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:68771301..68771502 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1769452,Human_RBP_ID_4124153,Human_RBP_ID_5545749,Human_RBP_ID_5991076,Human_RBP_ID_17460540,Human_RBP_ID_18525079,Human_RBP_ID_22788482,Human_RBP_ID_22883719,Human_RBP_ID_23464616 Human_Splice_Rec_1139687,Human_Splice_Rec_1139741,Human_Splice_Rec_1139845,Human_Splice_Rec_1139887,Human_Splice_Rec_1139993 RMVar_hsa_circ_14730,RMVar_hsa_circ_307164,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_115064,RMVar_hsa_circ_143889,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_337764,RMVar_hsa_circ_6320,RMVar_hsa_circ_29756,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901,RMVar_hsa_circ_280012,RMVar_hsa_circ_276902,RMVar_hsa_circ_143904,RMVar_hsa_circ_268652,RMVar_hsa_circ_143905,RMVar_hsa_circ_143906,RMVar_hsa_circ_368301,RMVar_hsa_circ_311164,RMVar_hsa_circ_38883,RMVar_hsa_circ_289248,RMVar_hsa_circ_308624,RMVar_hsa_circ_353284,RMVar_hsa_circ_334686,RMVar_hsa_circ_143908,RMVar_hsa_circ_143909,RMVar_hsa_circ_355245,RMVar_hsa_circ_366077,RMVar_hsa_circ_71115,RMVar_hsa_circ_298943,RMVar_hsa_circ_143910,RMVar_hsa_circ_27926,RMVar_hsa_circ_328433,RMVar_hsa_circ_348162,RMVar_hsa_circ_143912,RMVar_hsa_circ_69537,RMVar_hsa_circ_143911 115636 RMVar_ID_115636 Human_SNP_ID_809520677 m1A Human chr10 - 1396817 1396817 1396817 ACCCAGGAAGCCTCCACTCGGGAGGGGAGAGGAGGACGGTGACCCAGGAAGCCTCCACTCGGGAG ACCCAGGAAGCCTCCACTCGGGAGGGGAGAGGCGGACGGTGACCCAGGAAGCCTCCACTCGGGAG T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:1396815..1396980 26863196 MeRIP-seq:(Medium) rs4880505 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115637 RMVar_ID_115637 Human_SNP_ID_809545635 m1A Human chr10 - 22714334 22714334 22714334 CCTCGGGAGCACGGCGGTGGAGGGGACATAGGAGGCGGCCATGGCGACCCCCGGCAACCTAGGGT CCTCGGGAGCACGGCGGTGGAGGGGACATAGGTGGCGGCCATGGCGACCCCCGGCAACCTAGGGT T A PIP4K2A Ensembl:ENSG00000150867 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr10:22714294..22714523 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_192139,Human_RBP_ID_4136190,Human_RBP_ID_5313186,Human_RBP_ID_5956303,Human_RBP_ID_8172126,Human_RBP_ID_9320513,Human_RBP_ID_18456049,Human_RBP_ID_18475990 115638 RMVar_ID_115638 Human_SNP_ID_809554580 m1A Human chr10 + 90872066 90872066 90872066 GGCTCTGCGCGGACTTGTGGAGACAGCCGCTCACCGTGAGTTGCCCCGGCTTCGCGCCTGGCCAA GGCTCTGCGCGGACTTGTGGAGACAGCCGCTCTCCGTGAGTTGCCCCGGCTTCGCGCCTGGCCAA A T RPP30 Ensembl:ENSG00000148688 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr10:90872016..90872122;chr10:90872016..90872119 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_274085,Human_RBP_ID_748117,Human_RBP_ID_4131676,Human_RBP_ID_19046862,Human_RBP_ID_22431538,Human_RBP_ID_23117812 Human_Splice_Rec_1159329,Human_Splice_Rec_1159349,Human_Splice_Rec_1159373,Human_Splice_Rec_1159391 115639 RMVar_ID_115639 Human_SNP_ID_809580231 m1A Human chr10 + 117358513 117358513 117358513 GACTATAAAATAGTCTTTTTTACTGATTGCTAACCCTTAGTCCTCACTGCTGCATTCCACACCTA GACTATAAAATAGTCTTTTTTACTGATTGCTAGCCCTTAGTCCTCACTGCTGCATTCCACACCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:117358510..117358592 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 115640 RMVar_ID_115640 Human_SNP_ID_809653094 m1A Human chr10 - 99923742 99923742 99923742 GAGAAGCAAGGAGAACAGTTCTGGTTGGGGAAACTATGAGAAAGACATAGGGTTGTGGTGACAAA GAGAAGCAAGGAGAACAGTTCTGGTTGGGGAAGCTATGAGAAAGACATAGGGTTGTGGTGACAAA T C DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:99923694..99923789 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LMS 1 - RMVar_hsa_circ_51010 115641 RMVar_ID_115641 Human_SNP_ID_809659496 m1A Human chr10 + 100979017 100979017 100979017 TCACCGTGTGGCCCGTGTGGCTCGTGTCTGCAAGGTGGATTGGGCTGACGTTGGGGCACGGGTAT TCACCGTGTGGCCCGTGTGGCTCGTGTCTGCATGGTGGATTGGGCTGACGTTGGGGCACGGGTAT A T SEMA4G Ensembl:ENSG00000095539 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:100979013..100979116 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney Human_RBP_ID_18970275,Human_RBP_ID_23429009 Human_Splice_Rec_1169245,Human_Splice_Rec_1169269,Human_Splice_Rec_1169311,Human_Splice_Rec_1169337,Human_Splice_Rec_1169363 RMVar_hsa_circ_351767,RMVar_hsa_circ_343428,RMVar_hsa_circ_145679 115642 RMVar_ID_115642 Human_SNP_ID_809673868 m1A Human chr10 - 124791763 124791763 124791763 GGCGGCGCGGTCGGACAAGGGCAGTCCCGGGGAGGACGGTTTCGTCCCGTCGGCGCTGGGGACCC GGCGGCGCGGTCGGACAAGGGCAGTCCCGGGGTGGACGGTTTCGTCCCGTCGGCGCTGGGGACCC T A EEF1AKMT2 Ensembl:ENSG00000203791 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr10:124790285..124791771 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_373288,Human_RBP_ID_4136558,Human_RBP_ID_18416200,Human_RBP_ID_22886685 Human_Splice_Rec_1186439,Human_Splice_Rec_1186491,Human_Splice_Rec_1186501,Human_Splice_Rec_1186513,Human_Splice_Rec_1186525 RMVar_hsa_circ_121172,RMVar_hsa_circ_146974 115643 RMVar_ID_115643 Human_SNP_ID_809686456 m1A Human chr10 + 68337275 68337275 68337275 AATGGTCCAAATGACGCTAGTGATGGGACAGTACGACTTCGTGGACTACCATTTGGTTGCAGCAA AATGGTCCAAATGACGCTAGTGATGGGACAGTGCGACTTCGTGGACTACCATTTGGTTGCAGCAA A G HNRNPH3 Ensembl:ENSG00000096746 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:68337226..68337350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_26497,Human_RBP_ID_380200,Human_RBP_ID_983971,Human_RBP_ID_1448604,Human_RBP_ID_1769038,Human_RBP_ID_4123697,Human_RBP_ID_5989343,Human_RBP_ID_8337291,Human_RBP_ID_8762328,Human_RBP_ID_8991212,Human_RBP_ID_11396448,Human_RBP_ID_18596383,Human_RBP_ID_19045375,Human_RBP_ID_23463902,Human_RBP_ID_24823777 Human_Splice_Rec_1139054,Human_Splice_Rec_1139068,Human_Splice_Rec_1139069,Human_Splice_Rec_1139076,Human_Splice_Rec_1139077,Human_Splice_Rec_1139094,Human_Splice_Rec_1139095,Human_Splice_Rec_1139104,Human_Splice_Rec_1139105,Human_Splice_Rec_1139112,Human_Splice_Rec_1139113,Human_Splice_Rec_1139118,Human_Splice_Rec_1139119 Human_miRNA_ID_2247109 RMVar_hsa_circ_45980,RMVar_hsa_circ_321716,RMVar_hsa_circ_359868,RMVar_hsa_circ_364113,RMVar_hsa_circ_376301,RMVar_hsa_circ_357669,RMVar_hsa_circ_84362,RMVar_hsa_circ_127023,RMVar_hsa_circ_74024,RMVar_hsa_circ_143734,RMVar_hsa_circ_143736,RMVar_hsa_circ_143737,RMVar_hsa_circ_143735,RMVar_hsa_circ_143733 115644 RMVar_ID_115644 Human_SNP_ID_809717066 m1A Human chr10 + 35667315 35667315 35667315 CCACCGCCACCACCATCATCACCACCACCACCATCATCACCACCATCACCACCACCACCACCATC CCACCGCCACCACCATCATCACCACCACCACCGTCATCACCACCATCACCACCACCACCACCATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:35667214..35667354 26863196 MeRIP-seq:(Medium) rs111208326 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115645 RMVar_ID_115645 Human_SNP_ID_809722983 m1A Human chr10 - 102157064 102157064 102157064 AAATGGAACAGGAAAGGCTTACTTGAGCCAGAAGCTATAGATGTCTAAGAGGGAAGAGGCATTGG AAATGGAACAGGAAAGGCTTACTTGAGCCAGACGCTATAGATGTCTAAGAGGGAAGAGGCATTGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr10:102157026..102157075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 115646 RMVar_ID_115646 Human_SNP_ID_809728803 m1A Human chr10 + 74825626 74825626 74825626 GGCGGAGGCTGAGGAAGGCAGCGGGGAGACCCAGGCTGCAGCAACAAAGGGCAGCGAGCGATTGG GGCGGAGGCTGAGGAAGGCAGCGGGGAGACCCGGGCTGCAGCAACAAAGGGCAGCGAGCGATTGG A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:74825431..74825830 26863196 MeRIP-seq:(Medium) rs1011043249 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_862480 Human_Splice_Rec_1148735,Human_Splice_Rec_1148769,Human_Splice_Rec_1148801,Human_Splice_Rec_1148829,Human_Splice_Rec_1148863,Human_Splice_Rec_1148893,Human_Splice_Rec_1148899 115647 RMVar_ID_115647 Human_SNP_ID_809739747 m1A Human chr10 - 102382156 102382156 102382156 TGCAGGATCAGTGGGGGCTGAGCCAAGGGTGGAGGCCCGTCGGGGGTGGGGCTCAGCCTGCTGGG TGCAGGATCAGTGGGGGCTGAGCCAAGGGTGGGGGCCCGTCGGGGGTGGGGCTCAGCCTGCTGGG T C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:102382035..102382325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain 115648 RMVar_ID_115648 Human_SNP_ID_809747371 m1A Human chr10 - 92593175 92593175 92593175 TCTGGCCGTGGCGTTTGTCCCGCGCCAGTCGGAGCCGCCAAATCACTAATCTCGTCTCCGCCCGA TCTGGCCGTGGCGTTTGTCCCGCGCCAGTCGGGGCCGCCAAATCACTAATCTCGTCTCCGCCCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr10:92593126..92593402;chr10:92593126..92593393 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 115649 RMVar_ID_115649 Human_SNP_ID_809774886 m1A Human chr10 + 62805851 62805851 62805851 GATGACTTCTGGTGCGAGGGAGAACCCTATCCAGGTCCCAAGGTCTTCCCTTGAAGCCACTGGCG GATGACTTCTGGTGCGAGGGAGAACCCTATCCGGGTCCCAAGGTCTTCCCTTGAAGCCACTGGCG A G ADO Ensembl:ENSG00000181915 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr10:62805800..62805900 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1159268,Human_RBP_ID_26880444,Human_RBP_ID_27193964,Human_RBP_ID_27802707 115650 RMVar_ID_115650 Human_SNP_ID_809804394 m1A Human chr10 - 73523665 73523664 73523665 AGGAGGGCGCAGGAACAGGAACTTCGAAGAAAACGGGAGAAGGAGTTAGAGGCAGCGAAAGGGTT AGGAGGGCGCAGGAACAGGAACTTCGAAGAAA_CGGGAGAAGGAGTTAGAGGCAGCGAAAGGGTT GT G USP54 Ensembl:ENSG00000166348 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:73523553..73523707 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_18597965 Human_Splice_Rec_1146466,Human_Splice_Rec_1146467,Human_Splice_Rec_1146482,Human_Splice_Rec_1146483,Human_Splice_Rec_1146510,Human_Splice_Rec_1146511,Human_Splice_Rec_1146548,Human_Splice_Rec_1146549,Human_Splice_Rec_1146584,Human_Splice_Rec_1146585,Human_Splice_Rec_1146596,Human_Splice_Rec_1146597,Human_Splice_Rec_1146634,Human_Splice_Rec_1146635 RMVar_hsa_circ_42724,RMVar_hsa_circ_91450,RMVar_hsa_circ_110450,RMVar_hsa_circ_144318,RMVar_hsa_circ_144319,RMVar_hsa_circ_3773,RMVar_hsa_circ_65447,RMVar_hsa_circ_35904,RMVar_hsa_circ_378301 115651 RMVar_ID_115651 Human_SNP_ID_809850803 m1A Human chr10 + 102133114 102133114 102133114 GGGGACGGAGAGACGGAGTCGCGCCGCCCCCGAGTGGGGGCCCCGGTCCGGACCCTGGCGGGGGA GGGGACGGAGAGACGGAGTCGCGCCGCCCCCGTGTGGGGGCCCCGGTCCGGACCCTGGCGGGGGA A T PPRC1 Ensembl:ENSG00000148840 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr10:102133051..102133225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_4136485,Human_RBP_ID_5138168,Human_RBP_ID_5520260 115652 RMVar_ID_115652 Human_SNP_ID_809852300 m1A Human chr10 + 1653593 1653593 1653593 CTCCACCCCACGCCTCATGTGCCTGCAGAGCCACAGTCTCCACCCAACGCCTTCTGTGCCTGCAG CTCCACCCCACGCCTCATGTGCCTGCAGAGCCGCAGTCTCCACCCAACGCCTTCTGTGCCTGCAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:1653584..1653650 26863196 MeRIP-seq:(Medium) rs1417011293 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115653 RMVar_ID_115653 Human_SNP_ID_809856661 m1A Human chr10 - 133569584 133569584 133569584 TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGGAGCCGGGTGCGGGGGTCGCGGGGGACCGCGGGG TGGAGGGGCAGGAAGCACGGCGGGTGGAGCGGGGCCGGGTGCGGGGGTCGCGGGGGACCGCGGGG T C SYCE1 Ensembl:ENSG00000171772 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr10:133569536..133569649;chr10:133569536..133569708;chr10:133569536..133569642;chr10:133569528..133569654;chr10:133569525..133569655 26863196 MeRIP-seq:(Medium) rs532152451 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue 115654 RMVar_ID_115654 Human_SNP_ID_809857342 m1A Human chr10 - 35642143 35642143 35642143 CCTGGGTGTCCAGCAGGAAGGAGACTGTGTGCACCTCGCCCGACTGCGGCCGGAGCGCGGCGCTG CCTGGGTGTCCAGCAGGAAGGAGACTGTGTGCGCCTCGCCCGACTGCGGCCGGAGCGCGGCGCTG T C FZD8 Ensembl:ENSG00000177283 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:35641986..35642239 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4119050 115655 RMVar_ID_115655 Human_SNP_ID_809870779 m1A Human chr10 + 91923871 91923871 91923871 TCGGAGGACTGCCGCCTCCGCTACCGTCTTGGACCCCTGCTTACCGGCCGCCGCGGGGACGAGCT TCGGAGGACTGCCGCCTCCGCTACCGTCTTGGCCCCCTGCTTACCGGCCGCCGCGGGGACGAGCT A C BTAF1 Ensembl:ENSG00000095564 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr10:91923801..91924000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_225681,Human_RBP_ID_748425,Human_RBP_ID_862574,Human_RBP_ID_1451628,Human_RBP_ID_4135953,Human_RBP_ID_5435799,Human_RBP_ID_5520481,Human_RBP_ID_26316509,Human_RBP_ID_27802211 115656 RMVar_ID_115656 Human_SNP_ID_809879664 m1A Human chr10 + 12167751 12167751 12167751 GCACTTCAAATGGCTTTGCATTTGCATGTTTCAGTGCTAGAGCGTAGGAATAGACCCTGGCGTCC GCACTTCAAATGGCTTTGCATTTGCATGTTTCCGTGCTAGAGCGTAGGAATAGACCCTGGCGTCC A C SEC61A2 Ensembl:ENSG00000065665 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr10:12167701..12169769 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - RMVar_hsa_circ_361761 115657 RMVar_ID_115657 Human_SNP_ID_809880027 m1A Human chr10 + 119672385 119672385 119672385 GCGGGGGTACATCTCCATTCCGGTGATACACGAGCAGAACGTTACCCGGCCAGCAGCCCAGCCCT GCGGGGGTACATCTCCATTCCGGTGATACACGGGCAGAACGTTACCCGGCCAGCAGCCCAGCCCT A G BAG3 Ensembl:ENSG00000151929 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr10:119672334..119672415 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_225867 RMVar_hsa_circ_302981 115658 RMVar_ID_115658 Human_SNP_ID_809881025 m1A Human chr10 + 34642437 34642437 34642437 TGCCTCTCACGGCCTTCCACTCACTCTGCCCCACACCCTGGCTCTGCCTCACCAGCCTGCTCTTC TGCCTCTCACGGCCTTCCACTCACTCTGCCCCCCACCCTGGCTCTGCCTCACCAGCCTGCTCTTC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:34642390..34642505 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115659 RMVar_ID_115659 Human_SNP_ID_809911685 m1A Human chr10 - 75235710 75235710 75235710 GAGGCGGTGCCCCCCATGGCGAGGCCGGCGAGAGCAGTGCCTGCTTCCCCCCGAGGACAGCCGCC GAGGCGGTGCCCCCCATGGCGAGGCCGGCGAGGGCAGTGCCTGCTTCCCCCCGAGGACAGCCGCC T C COMTD1 Ensembl:ENSG00000165644 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr10:75235609..75235780 26863196 MeRIP-seq:(Medium) rs558946859 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 1 head and neck Human_RBP_ID_383008,Human_RBP_ID_19045471 Human_Splice_Rec_1149788,Human_Splice_Rec_1149789,Human_Splice_Rec_1149820,Human_Splice_Rec_1149835 RMVar_hsa_circ_144477,RMVar_hsa_circ_122572 115660 RMVar_ID_115660 Human_SNP_ID_872149506 m1A Human chr8 - 140532487 140532487 140532487 TACGTGCGCTGCACACGCTCCGTGTCCATCCCAGCGCCAGCATACTACGCTCACCTGGTGGCCTT TACGTGCGCTGCACACGCTCCGTGTCCATCCCTGCGCCAGCATACTACGCTCACCTGGTGGCCTT T A AGO2 Ensembl:ENSG00000123908 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:140532476..140532500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung Human_RBP_ID_8222469,Human_RBP_ID_8916988,Human_RBP_ID_9314035,Human_RBP_ID_18892677,Human_RBP_ID_26832439 Human_Splice_Rec_1015823,Human_Splice_Rec_1015855,Human_Splice_Rec_1015887,Human_Splice_Rec_1015889 RMVar_hsa_circ_90223,RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_269304,RMVar_hsa_circ_254672,RMVar_hsa_circ_254673 115661 RMVar_ID_115661 Human_SNP_ID_872170844 m1A Human chr8 - 25410199 25410199 25410199 GCCACAGTTGCCAGCTGTGATTTCCCTACCTCAGTGGAGTTCCTCTGGCTGCCTTCATAGGGCTT GCCACAGTTGCCAGCTGTGATTTCCCTACCTCGGTGGAGTTCCTCTGGCTGCCTTCATAGGGCTT T C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:25410176..25410225 26863196 MeRIP-seq:(Medium) rs1310284339 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115662 RMVar_ID_115662 Human_SNP_ID_872197246 m1A Human chr8 + 100704980 100704980 100704980 GACTCGAGCATATGAAGAAGTTCTGAATTATCAATCTCCAACAACATGCCAGTGATTTTACCAGC GACTCGAGCATATGAAGAAGTTCTGAATTATCTATCTCCAACAACATGCCAGTGATTTTACCAGC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:100704925..100705055 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine 115663 RMVar_ID_115663 Human_SNP_ID_872199932 m1A Human chr8 - 100721583 100721583 100721583 CGGCCTGTGGCCCTGCGGGCAGCCGTGCCGAGATGAACCCCAGTGCCCCCAGCTACCCCATGGCC CGGCCTGTGGCCCTGCGGGCAGCCGTGCCGAGGTGAACCCCAGTGCCCCCAGCTACCCCATGGCC T C PABPC1 Ensembl:ENSG00000070756 Protein coding start codon GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:100721535..100721824 26863196 MeRIP-seq:(Medium) rs1243077943 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_691985,Human_RBP_ID_795228,Human_RBP_ID_8676412,Human_RBP_ID_16300227,Human_RBP_ID_17433955,Human_RBP_ID_17543954,Human_RBP_ID_18889198,Human_RBP_ID_18961602,Human_RBP_ID_22534381,Human_RBP_ID_26141203,Human_RBP_ID_26552678,Human_RBP_ID_27119386 Human_Splice_Rec_997652,Human_Splice_Rec_997800,Human_Splice_Rec_997804,Human_Splice_Rec_997814 RMVar_hsa_circ_98534,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_253549 115664 RMVar_ID_115664 Human_SNP_ID_872220333 m1A Human chr8 + 73008917 73008917 73008917 ACATGGCGGAGGATGTTTCCTCAGCGGCCCCGAGCCCGCGGGGCTGTGCGGATGGTAGGGATGCC ACATGGCGGAGGATGTTTCCTCAGCGGCCCCGCGCCCGCGGGGCTGTGCGGATGGTAGGGATGCC A C TERF1 Ensembl:ENSG00000147601 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:73008876..73009079;chr8:73008876..73009166;chr8:73008876..73009126;chr8:73008876..73009110 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary Human_RBP_ID_4995561,Human_RBP_ID_9405558 115665 RMVar_ID_115665 Human_SNP_ID_872245686 m1A Human chr8 - 73292787 73292784 73292787 CATTTTTGTTTATTAACGTTAGAGAGAAGAAGAAGGAGGTTCCTGCTGTGCCAGAAACCCTTAAG CATTTTTGTTTATTAACGTTAGAGAGAAGAAG___GAGGTTCCTGCTGTGCCAGAAACCCTTAAG CCTT C RPL7 Ensembl:ENSG00000147604 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:73292654..73292825 26863410 MeRIP-seq:(Medium) rs556746526 Functional Loss DEL ICGC 33..35 33 ORCA 1 - Human_RBP_ID_254881,Human_RBP_ID_16469095,Human_RBP_ID_17665965,Human_RBP_ID_24391634,Human_RBP_ID_24549456,Human_RBP_ID_26181672 Human_Splice_Rec_986026,Human_Splice_Rec_986027,Human_Splice_Rec_986040,Human_Splice_Rec_986041,Human_Splice_Rec_986050,Human_Splice_Rec_986051,Human_Splice_Rec_986060,Human_Splice_Rec_986061,Human_Splice_Rec_986072,Human_Splice_Rec_986073,Human_Splice_Rec_986078,Human_Splice_Rec_986079 Human_miRNA_ID_2221270,Human_miRNA_ID_2484316,Human_miRNA_ID_3072695,Human_miRNA_ID_3088051 RMVar_hsa_circ_76234,RMVar_hsa_circ_252730,RMVar_hsa_circ_68230 115666 RMVar_ID_115666 Human_SNP_ID_872292562 m1A Human chr8 + 100557247 100557247 100557247 GACTAAAACTGGCTCCACCTACCTTCACACTCAGTCTTCTCCATCTCAGTACACTGTTTAACTAA GACTAAAACTGGCTCCACCTACCTTCACACTCCGTCTTCTCCATCTCAGTACACTGTTTAACTAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:100557197..100557556 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115667 RMVar_ID_115667 Human_SNP_ID_872314947 m1A Human chr8 + 85115183 85115183 85115183 GCAAGAACATATTTGGTGAACCAGTAAATTTGACAGAAATAAATTCATCACAGCTGCAGTGCCTA GCAAGAACATATTTGGTGAACCAGTAAATTTGGCAGAAATAAATTCATCACAGCTGCAGTGCCTA A G LRRCC1 Ensembl:ENSG00000133739 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3736038 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_989160,Human_Splice_Rec_989161,Human_Splice_Rec_989188,Human_Splice_Rec_989189,Human_Splice_Rec_989218,Human_Splice_Rec_989219,Human_Splice_Rec_989252,Human_Splice_Rec_989253 GWAS_ID_13697,GWAS_ID_13698,GWAS_ID_13699,GWAS_ID_13700 RMVar_hsa_circ_10267,RMVar_hsa_circ_296745,RMVar_hsa_circ_333387,RMVar_hsa_circ_346496,RMVar_hsa_circ_305075,RMVar_hsa_circ_284787,RMVar_hsa_circ_252878,RMVar_hsa_circ_252880,RMVar_hsa_circ_252881,RMVar_hsa_circ_252882,RMVar_hsa_circ_252879,RMVar_hsa_circ_18976,RMVar_hsa_circ_252883,RMVar_hsa_circ_102791 115668 RMVar_ID_115668 Human_SNP_ID_872327706 m1A Human chr8 + 135607029 135607029 135607029 TATGATTCCTATGATAACAGCTATAGCACCCCAGCCCAAAGGTAAGAGTCAGTCTTTATTACCAG TATGATTCCTATGATAACAGCTATAGCACCCCGGCCCAAAGGTAAGAGTCAGTCTTTATTACCAG A G KHDRBS3 Ensembl:ENSG00000131773 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:135607007..135647054 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1014602,Human_Splice_Rec_1014603,Human_Splice_Rec_1014618,Human_Splice_Rec_1014622,Human_Splice_Rec_1014623,Human_Splice_Rec_1014658,Human_Splice_Rec_1014659,Human_Splice_Rec_1014664,Human_Splice_Rec_1014665,Human_Splice_Rec_1014669,Human_Splice_Rec_1014671 RMVar_hsa_circ_14985,RMVar_hsa_circ_319072,RMVar_hsa_circ_254600,RMVar_hsa_circ_254596,RMVar_hsa_circ_294276,RMVar_hsa_circ_254605,RMVar_hsa_circ_330740,RMVar_hsa_circ_301813,RMVar_hsa_circ_254607,RMVar_hsa_circ_254610,RMVar_hsa_circ_321908,RMVar_hsa_circ_303533,RMVar_hsa_circ_254611 115669 RMVar_ID_115669 Human_SNP_ID_872344102 m1A Human chr8 - 23309821 23309821 23309821 CCGGCCCATGTTCATGCTGCAGTGTGCCATGGAGGAGAACTGCCTCTCGGCCTCAGCCGCGCAGA CCGGCCCATGTTCATGCTGCAGTGTGCCATGGTGGAGAACTGCCTCTCGGCCTCAGCCGCGCAGA T A LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:23309651..23309850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_958488 Human_miRNA_ID_2279605,Human_miRNA_ID_2459666,Human_miRNA_ID_2639898 RMVar_hsa_circ_11094,RMVar_hsa_circ_45914,RMVar_hsa_circ_28168,RMVar_hsa_circ_53278,RMVar_hsa_circ_250782,RMVar_hsa_circ_109885,RMVar_hsa_circ_331761,RMVar_hsa_circ_343155,RMVar_hsa_circ_348092,RMVar_hsa_circ_118425,RMVar_hsa_circ_250783 115670 RMVar_ID_115670 Human_SNP_ID_872344105 m1A Human chr8 - 23309821 23309821 23309821 CCGGCCCATGTTCATGCTGCAGTGTGCCATGGAGGAGAACTGCCTCTCGGCCTCAGCCGCGCAGA CCGGCCCATGTTCATGCTGCAGTGTGCCATGGCGGAGAACTGCCTCTCGGCCTCAGCCGCGCAGA T G LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:23309651..23309850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney Human_Splice_Rec_958488 Human_miRNA_ID_2279605,Human_miRNA_ID_2459666,Human_miRNA_ID_2639898 RMVar_hsa_circ_11094,RMVar_hsa_circ_45914,RMVar_hsa_circ_28168,RMVar_hsa_circ_53278,RMVar_hsa_circ_250782,RMVar_hsa_circ_109885,RMVar_hsa_circ_331761,RMVar_hsa_circ_343155,RMVar_hsa_circ_348092,RMVar_hsa_circ_118425,RMVar_hsa_circ_250783 115671 RMVar_ID_115671 Human_SNP_ID_872346522 m1A Human chr8 - 143934366 143934366 143934366 GCTGGATGTGGAGAAGGAGTGGGGCAAGCTGCACGTGGCCATCCTGGAGCGGGAGAAGCAGCTCC GCTGGATGTGGAGAAGGAGTGGGGCAAGCTGCGCGTGGCCATCCTGGAGCGGGAGAAGCAGCTCC T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143934300..143934450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 9 lung Human_RBP_ID_89195,Human_RBP_ID_3974217,Human_RBP_ID_18472627,Human_RBP_ID_19023230,Human_RBP_ID_22465038 Human_Splice_Rec_1021360,Human_Splice_Rec_1021361,Human_Splice_Rec_1021420,Human_Splice_Rec_1021421,Human_Splice_Rec_1021480,Human_Splice_Rec_1021481,Human_Splice_Rec_1021540,Human_Splice_Rec_1021541,Human_Splice_Rec_1021600,Human_Splice_Rec_1021601,Human_Splice_Rec_1021660,Human_Splice_Rec_1021661,Human_Splice_Rec_1021720,Human_Splice_Rec_1021721,Human_Splice_Rec_1021780,Human_Splice_Rec_1021781,Human_Splice_Rec_1021840,Human_Splice_Rec_1021841,Human_Splice_Rec_1021898,Human_Splice_Rec_1021899,Human_Splice_Rec_1021962,Human_Splice_Rec_1021963 Human_miRNA_ID_207166,Human_miRNA_ID_1490935,Human_miRNA_ID_2012517,Human_miRNA_ID_2012518,Human_miRNA_ID_2674861,Human_miRNA_ID_2674862,Human_miRNA_ID_2758893,Human_miRNA_ID_2758894,Human_miRNA_ID_2925614,Human_miRNA_ID_2925615 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_85553,RMVar_hsa_circ_3035,RMVar_hsa_circ_254972,RMVar_hsa_circ_254974,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985,RMVar_hsa_circ_99232,RMVar_hsa_circ_121074,RMVar_hsa_circ_254988,RMVar_hsa_circ_254987,RMVar_hsa_circ_10998,RMVar_hsa_circ_57497,RMVar_hsa_circ_108803,RMVar_hsa_circ_108144,RMVar_hsa_circ_254989,RMVar_hsa_circ_254991,RMVar_hsa_circ_96142,RMVar_hsa_circ_254990 115672 RMVar_ID_115672 Human_SNP_ID_872354490 m1A Human chr8 - 122877846 122877846 122877846 AAGAATCTGCCTATTGTAGAGTCAATCAAACCAGATCGTGCTTCCTTCTCCAAATGCAGTCCATA AAGAATCTGCCTATTGTAGAGTCAATCAAACCGGATCGTGCTTCCTTCTCCAAATGCAGTCCATA T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:122877741..122877870 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115673 RMVar_ID_115673 Human_SNP_ID_872415136 m1A Human chr8 + 1903315 1903315 1903315 CATGCTGAAGAACACCTCCAAAGGCCACCCCGACAGGCTGCCTCTTCAGATGGCCCTGACAGAGC CATGCTGAAGAACACCTCCAAAGGCCACCCCGGCAGGCTGCCTCTTCAGATGGCCCTGACAGAGC A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:1903291..1903491 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_27831672 Human_Splice_Rec_944674,Human_Splice_Rec_944728,Human_Splice_Rec_944800,Human_Splice_Rec_944854,Human_Splice_Rec_944912,Human_Splice_Rec_944968,Human_Splice_Rec_945026,Human_Splice_Rec_945048,Human_Splice_Rec_945068,Human_Splice_Rec_945094 Human_miRNA_ID_2225189 RMVar_hsa_circ_9345,RMVar_hsa_circ_98986,RMVar_hsa_circ_374483,RMVar_hsa_circ_327755,RMVar_hsa_circ_103644,RMVar_hsa_circ_249989,RMVar_hsa_circ_249990,RMVar_hsa_circ_249987,RMVar_hsa_circ_249988,RMVar_hsa_circ_29318,RMVar_hsa_circ_249996,RMVar_hsa_circ_347372,RMVar_hsa_circ_68999,RMVar_hsa_circ_274257,RMVar_hsa_circ_59376,RMVar_hsa_circ_116441,RMVar_hsa_circ_249998,RMVar_hsa_circ_326331,RMVar_hsa_circ_250003,RMVar_hsa_circ_250004,RMVar_hsa_circ_67013,RMVar_hsa_circ_250008,RMVar_hsa_circ_122082,RMVar_hsa_circ_112063,RMVar_hsa_circ_265253,RMVar_hsa_circ_250006,RMVar_hsa_circ_81593,RMVar_hsa_circ_250007 115674 RMVar_ID_115674 Human_SNP_ID_872423942 m1A Human chr8 - 143850993 143850991 143850993 GTGATGGGTTACCCTGGGGACAGTGAGAAGGAAAGGCAGAGACAGAGGAGCTCAGATGCCTGGCT GTGATGGGTTACCCTGGGGACAGTGAGAAGGA__GGCAGAGACAGAGGAGCTCAGATGCCTGGCT CTT C lnc-EPPK1-2 RNACentral:URS0000D5BCBE lincRNA exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143850984..143851108 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - 115675 RMVar_ID_115675 Human_SNP_ID_872429573 m1A Human chr8 + 60853320 60853320 60853320 AGGGCAAAGAAGAGGAAGAAGAAACCGATGGCAGCGGGAAGGAGAGCAAGCAGGAATGTGAGGCA AGGGCAAAGAAGAGGAAGAAGAAACCGATGGCGGCGGGAAGGAGAGCAAGCAGGAATGTGAGGCA A G CHD7 Ensembl:ENSG00000171316 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:60853273..60853414 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_89090 RMVar_hsa_circ_76107,RMVar_hsa_circ_252259,RMVar_hsa_circ_269627,RMVar_hsa_circ_73304,RMVar_hsa_circ_267861,RMVar_hsa_circ_107755,RMVar_hsa_circ_252283,RMVar_hsa_circ_55334 115676 RMVar_ID_115676 Human_SNP_ID_872521500 m1A Human chr8 + 123541136 123541136 123541136 GGGGCCCGCGACGGGGGCGGCGGGGCGGCGGGAACGGCGCGGGGCACCCTGCGGGGTGGCGGGCG GGGGCCCGCGACGGGGGCGGCGGGGCGGCGGGGACGGCGCGGGGCACCCTGCGGGGTGGCGGGCG A G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:123541045..123541175 26863410 MeRIP-seq:(Medium) rs1410432651 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115677 RMVar_ID_115677 Human_SNP_ID_872528121 m1A Human chr8 + 127736475 127736475 127736475 GCGGGCGGGCACTTTGCACTGGAACTTACAACACCCGAGCAAGGACGCGACTCTCCCGACGCGGG GCGGGCGGGCACTTTGCACTGGAACTTACAACGCCCGAGCAAGGACGCGACTCTCCCGACGCGGG A G MYC Ensembl:ENSG00000136997 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:127736301..127736475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 20 haematopoietic and lymphoid tissue Human_RBP_ID_88454,Human_RBP_ID_3140041,Human_RBP_ID_4997934,Human_RBP_ID_5154190,Human_RBP_ID_5223266,Human_RBP_ID_5430170,Human_RBP_ID_16352723,Human_RBP_ID_22115153,Human_RBP_ID_26832419,Human_RBP_ID_27535924 Human_Splice_Rec_1008888 RMVar_hsa_circ_76158,RMVar_hsa_circ_111351,RMVar_hsa_circ_254315,RMVar_hsa_circ_254316 115678 RMVar_ID_115678 Human_SNP_ID_872528127 m1A Human chr8 + 127736475 127736475 127736475 GCGGGCGGGCACTTTGCACTGGAACTTACAACACCCGAGCAAGGACGCGACTCTCCCGACGCGGG GCGGGCGGGCACTTTGCACTGGAACTTACAACTCCCGAGCAAGGACGCGACTCTCCCGACGCGGG A T MYC Ensembl:ENSG00000136997 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:127736301..127736475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_88454,Human_RBP_ID_3140041,Human_RBP_ID_4997934,Human_RBP_ID_5154190,Human_RBP_ID_5223266,Human_RBP_ID_5430170,Human_RBP_ID_16352723,Human_RBP_ID_22115153,Human_RBP_ID_26832419,Human_RBP_ID_27535924 Human_Splice_Rec_1008888 RMVar_hsa_circ_76158,RMVar_hsa_circ_111351,RMVar_hsa_circ_254315,RMVar_hsa_circ_254316 115679 RMVar_ID_115679 Human_SNP_ID_872546442 m1A Human chr8 - 143867262 143867262 143867262 TCCCGCTGTTCCAGGCCATGCAGAAGCAGCTCATCGAGAAGGCGGAGGCACTGAGGCTGCTGGAG TCCCGCTGTTCCAGGCCATGCAGAAGCAGCTCGTCGAGAAGGCGGAGGCACTGAGGCTGCTGGAG T C EPPK1 Ensembl:ENSG00000261150 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143867252..143867387 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_18114041 115680 RMVar_ID_115680 Human_SNP_ID_872573743 m1A Human chr8 - 142736085 142736085 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTGGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs3736010 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 1 brain 115681 RMVar_ID_115681 Human_SNP_ID_872578834 m1A Human chr8 + 27748215 27748215 27748215 CTTTCTCTGCTGCTAGGTCTGGGAACCGCTCGACTTTGGTCTTTTCTAATCGGTTCAGGATCTCA CTTTCTCTGCTGCTAGGTCTGGGAACCGCTCGTCTTTGGTCTTTTCTAATCGGTTCAGGATCTCA A T AC013643.2 Ensembl:ENSG00000253875 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:27748059..27748217 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115682 RMVar_ID_115682 Human_SNP_ID_872630607 m1A Human chr8 + 145052608 145052608 145052608 CTTTCTCCAGGCCCTGGGACATCTTGCTGGGGAGGCAGCGGCGGCCCCAGGCCCGGGTACTCCCT CTTTCTCCAGGCCCTGGGACATCTTGCTGGGGCGGCAGCGGCGGCCCCAGGCCCGGGTACTCCCT A C C8orf33 Ensembl:ENSG00000182307 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:145052476..145052725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4976185,Human_RBP_ID_18114396,Human_RBP_ID_22115326 Human_Splice_Rec_1025740,Human_Splice_Rec_1025750,Human_Splice_Rec_1025758,Human_Splice_Rec_1025768,Human_Splice_Rec_1025778 RMVar_hsa_circ_102981,RMVar_hsa_circ_107432,RMVar_hsa_circ_255212,RMVar_hsa_circ_255213 115683 RMVar_ID_115683 Human_SNP_ID_872637370 m1A Human chr8 + 126556160 126556160 126556160 AAGAATGGCCGATTATAAACCCAGATCTACCAAGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT AAGAATGGCCGATTATAAACCCAGATCTACCATGGTTTAAGTGCCAGGCAAGTCCACAGTTTGCT A T PCAT1 RNACentral:URS00009B75C9 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:126556109..126556259 32194978 MeRIP-seq:(Medium) rs967436456 Functional Loss SNV ICGC 33..33 33 LICA 1 - 115684 RMVar_ID_115684 Human_SNP_ID_872644292 m1A Human chr8 + 130016137 130016137 130016137 CTCGCGTCCGCCCGCCGCCCCCCGCGCACTCGAGGCGCCTCCCCCGGGACCCCCGCGCCCGCCGG CTCGCGTCCGCCCGCCGCCCCCCGCGCACTCGGGGCGCCTCCCCCGGGACCCCCGCGCCCGCCGG A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:130016091..130016230 26863196 MeRIP-seq:(Medium) rs959509756 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115685 RMVar_ID_115685 Human_SNP_ID_872700347 m1A Human chr8 + 11808795 11808795 11808795 TCCCACCGCCGTGTGTGTTGTCTGCCCGCAGGACTCGCTCAGCAGCAGCCTGAAAACTTGCTACA TCCCACCGCCGTGTGTGTTGTCTGCCCGCAGGGCTCGCTCAGCAGCAGCCTGAAAACTTGCTACA A G FDFT1 Ensembl:ENSG00000079459 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:11808776..11808800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_693313,Human_RBP_ID_960763,Human_RBP_ID_4995895,Human_RBP_ID_19021752,Human_RBP_ID_19139895,Human_RBP_ID_22465405,Human_RBP_ID_22626018,Human_RBP_ID_22775794,Human_RBP_ID_24241879,Human_RBP_ID_26360314,Human_RBP_ID_26795040 Human_Splice_Rec_949178,Human_Splice_Rec_949179,Human_Splice_Rec_949196,Human_Splice_Rec_949197,Human_Splice_Rec_949212,Human_Splice_Rec_949213,Human_Splice_Rec_949228,Human_Splice_Rec_949229,Human_Splice_Rec_949236,Human_Splice_Rec_949237,Human_Splice_Rec_949258,Human_Splice_Rec_949259,Human_Splice_Rec_949282,Human_Splice_Rec_949283,Human_Splice_Rec_949296,Human_Splice_Rec_949297,Human_Splice_Rec_949320,Human_Splice_Rec_949321,Human_Splice_Rec_949340,Human_Splice_Rec_949341,Human_Splice_Rec_949354,Human_Splice_Rec_949355,Human_Splice_Rec_949370,Human_Splice_Rec_949371,Human_Splice_Rec_949383,Human_Splice_Rec_949395,Human_Splice_Rec_949397,Human_Splice_Rec_949403 RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_127820,RMVar_hsa_circ_110343,RMVar_hsa_circ_250234,RMVar_hsa_circ_250235,RMVar_hsa_circ_288437,RMVar_hsa_circ_310262,RMVar_hsa_circ_250236,RMVar_hsa_circ_345764,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250240,RMVar_hsa_circ_250241,RMVar_hsa_circ_250239,RMVar_hsa_circ_250237 115686 RMVar_ID_115686 Human_SNP_ID_872727139 m1A Human chr8 - 47830687 47830687 47830687 AAAAATGAAGCAGGATGCCCAGGTCGTTCTGTACAGAAGCTACCGGCACGGAGACCTTCCTGACA AAAAATGAAGCAGGATGCCCAGGTCGTTCTGTGCAGAAGCTACCGGCACGGAGACCTTCCTGACA T C PRKDC Ensembl:ENSG00000253729 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:47830637..47830784 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_1070374,Human_RBP_ID_1336059,Human_RBP_ID_2055651,Human_RBP_ID_4987528,Human_RBP_ID_5629122,Human_RBP_ID_8920448,Human_RBP_ID_9313431,Human_RBP_ID_16427746,Human_RBP_ID_21905436,Human_RBP_ID_26832720 Human_Splice_Rec_975282,Human_Splice_Rec_975283,Human_Splice_Rec_975452,Human_Splice_Rec_975453 Human_miRNA_ID_2464828 RMVar_hsa_circ_119878,RMVar_hsa_circ_127746,RMVar_hsa_circ_125530,RMVar_hsa_circ_121996,RMVar_hsa_circ_115860,RMVar_hsa_circ_110848,RMVar_hsa_circ_106991,RMVar_hsa_circ_109431,RMVar_hsa_circ_106391,RMVar_hsa_circ_103570,RMVar_hsa_circ_105677,RMVar_hsa_circ_103064,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_85816,RMVar_hsa_circ_78885,RMVar_hsa_circ_251816,RMVar_hsa_circ_251813,RMVar_hsa_circ_251814,RMVar_hsa_circ_251812,RMVar_hsa_circ_251809,RMVar_hsa_circ_251810,RMVar_hsa_circ_251808,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_15990,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_125047,RMVar_hsa_circ_251825,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_104608,RMVar_hsa_circ_370867,RMVar_hsa_circ_251831,RMVar_hsa_circ_251836,RMVar_hsa_circ_117589,RMVar_hsa_circ_39715,RMVar_hsa_circ_251837,RMVar_hsa_circ_11362,RMVar_hsa_circ_110327,RMVar_hsa_circ_307126,RMVar_hsa_circ_251843,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_109579,RMVar_hsa_circ_251853,RMVar_hsa_circ_124485,RMVar_hsa_circ_251850,RMVar_hsa_circ_251851,RMVar_hsa_circ_127366,RMVar_hsa_circ_116027,RMVar_hsa_circ_251854,RMVar_hsa_circ_278197,RMVar_hsa_circ_112435,RMVar_hsa_circ_251852,RMVar_hsa_circ_361284,RMVar_hsa_circ_373300,RMVar_hsa_circ_251860,RMVar_hsa_circ_372942,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_71594,RMVar_hsa_circ_251863,RMVar_hsa_circ_31685,RMVar_hsa_circ_251864,RMVar_hsa_circ_251861,RMVar_hsa_circ_251862,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_266412,RMVar_hsa_circ_12669,RMVar_hsa_circ_56439,RMVar_hsa_circ_251867,RMVar_hsa_circ_85515,RMVar_hsa_circ_337032,RMVar_hsa_circ_355728,RMVar_hsa_circ_19420,RMVar_hsa_circ_34575,RMVar_hsa_circ_251868,RMVar_hsa_circ_115271,RMVar_hsa_circ_73006,RMVar_hsa_circ_367114 115687 RMVar_ID_115687 Human_SNP_ID_872751999 m1A Human chr8 - 143580561 143580559 143580562 GGAGGAGCGGCTACGGCAGTACGCGGAGAAGAAGGCCAAGAAGCCTGCACTGGTGGCCAAGTCCT GGAGGAGCGGCTACGGCAGTACGCGGAGAAG___GCCAAGAAGCCTGCACTGGTGGCCAAGTCCT CCTT C EEF1D Ensembl:ENSG00000104529 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143580480..143580751 26863196 MeRIP-seq:(Medium) rs756390399 Functional Loss DEL ICGC 32..34 33 COCA 1 - Human_RBP_ID_5123667,Human_RBP_ID_5153944,Human_RBP_ID_9405848,Human_RBP_ID_18125345,Human_RBP_ID_18196776,Human_RBP_ID_19022227,Human_RBP_ID_22465312 Human_Splice_Rec_1019465,Human_Splice_Rec_1019481,Human_Splice_Rec_1019495,Human_Splice_Rec_1019503,Human_Splice_Rec_1019507,Human_Splice_Rec_1019513,Human_Splice_Rec_1019527,Human_Splice_Rec_1019541,Human_Splice_Rec_1019559,Human_Splice_Rec_1019571,Human_Splice_Rec_1019582,Human_Splice_Rec_1019583,Human_Splice_Rec_1019597,Human_Splice_Rec_1019611,Human_Splice_Rec_1019624,Human_Splice_Rec_1019625,Human_Splice_Rec_1019637,Human_Splice_Rec_1019651,Human_Splice_Rec_1019666,Human_Splice_Rec_1019667,Human_Splice_Rec_1019683,Human_Splice_Rec_1019697,Human_Splice_Rec_1019700,Human_Splice_Rec_1019701,Human_Splice_Rec_1019711,Human_Splice_Rec_1019756 Human_miRNA_ID_1348976,Human_miRNA_ID_1812776,Human_miRNA_ID_2078472,Human_miRNA_ID_2080789,Human_miRNA_ID_2091336 RMVar_hsa_circ_94071,RMVar_hsa_circ_377557,RMVar_hsa_circ_254909,RMVar_hsa_circ_254910 115688 RMVar_ID_115688 Human_SNP_ID_872786830 m1A Human chr8 - 123370992 123370992 123370992 CAAATGTTAATGGCTTTTATTTAAACATTTTTAGAGCAATCTTAATATGTACACAAGAGGAAAAC CAAATGTTAATGGCTTTTATTTAAACATTTTTTGAGCAATCTTAATATGTACACAAGAGGAAAAC T A ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:123370901..123371000 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_7809354,Human_RBP_ID_17665847,Human_RBP_ID_22689312,Human_RBP_ID_26730374 Human_Splice_Rec_1005507,Human_Splice_Rec_1005559,Human_Splice_Rec_1005615,Human_Splice_Rec_1005669,Human_Splice_Rec_1005723 RMVar_hsa_circ_266235,RMVar_hsa_circ_338266,RMVar_hsa_circ_307644,RMVar_hsa_circ_254200,RMVar_hsa_circ_69779,RMVar_hsa_circ_254203,RMVar_hsa_circ_354799,RMVar_hsa_circ_284660,RMVar_hsa_circ_254204,RMVar_hsa_circ_254205,RMVar_hsa_circ_68072,RMVar_hsa_circ_359350,RMVar_hsa_circ_82743,RMVar_hsa_circ_72393,RMVar_hsa_circ_254208,RMVar_hsa_circ_254209,RMVar_hsa_circ_254211,RMVar_hsa_circ_354532,RMVar_hsa_circ_362895,RMVar_hsa_circ_265431,RMVar_hsa_circ_353920,RMVar_hsa_circ_268202,RMVar_hsa_circ_354950,RMVar_hsa_circ_267706,RMVar_hsa_circ_54047,RMVar_hsa_circ_366839 115689 RMVar_ID_115689 Human_SNP_ID_872798370 m1A Human chr8 - 143691085 143691060 143691085 CTCCCTTGAGAAGTAGATGGCCACGTCCCTGAAGGTCACTGGCTCCTGCAACACACACAGCTCCC CTCCCTTGAGAAGTAGATGGCCACGTCCCTGA_________________________CAGCTCCC GTGTGTGTTGCAGGAGCCAGTGACCT G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143691076..143691189 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..57 33 OV 1 - 115690 RMVar_ID_115690 Human_SNP_ID_872830074 m1A Human chr8 + 144523292 144523292 144523292 TGTGGGATACGTCCAGGAGACTCTGGAGCGCCAGGCGCGGGGGCTCTGCACACATGATCTTCCTG TGTGGGATACGTCCAGGAGACTCTGGAGCGCCGGGCGCGGGGGCTCTGCACACATGATCTTCCTG A G LRRC14 Ensembl:ENSG00000160959 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144523243..144523326 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 3 biliary tract,gallbladder Human_RBP_ID_89892,Human_RBP_ID_255403,Human_RBP_ID_18114217,Human_RBP_ID_21598448,Human_RBP_ID_22115636,Human_RBP_ID_22732152,Human_RBP_ID_23088031 Human_Splice_Rec_1025123,Human_Splice_Rec_1025127 115691 RMVar_ID_115691 Human_SNP_ID_872839975 m1A Human chr8 + 127738600 127738600 127738600 GACCGAGCTGCTGGGAGGAGACATGGTGAACCAGAGTTTCATCTGCGACCCGGACGACGAGACCT GACCGAGCTGCTGGGAGGAGACATGGTGAACCCGAGTTTCATCTGCGACCCGGACGACGAGACCT A C MYC Ensembl:ENSG00000136997 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:127738551..127738600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 5 haematopoietic and lymphoid tissue Human_RBP_ID_4970872,Human_RBP_ID_5628631,Human_RBP_ID_8923608,Human_RBP_ID_22328592,Human_RBP_ID_27362657,Human_RBP_ID_27535939 Human_miRNA_ID_2783857 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 115692 RMVar_ID_115692 Human_SNP_ID_872844022 m1A Human chr8 + 54459156 54459156 54459156 GCGTGCAGCACATGCAGGACCACCCCAACTACAAGTACCGGCCGCGGCGGCGCAAGCAGGTGAAG GCGTGCAGCACATGCAGGACCACCCCAACTACGAGTACCGGCCGCGGCGGCGCAAGCAGGTGAAG A G SOX17 Ensembl:ENSG00000164736 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:54459106..54459182 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_Splice_Rec_978236 115693 RMVar_ID_115693 Human_SNP_ID_872847949 m1A Human chr8 - 143986131 143986131 143986131 GAGCTGCTCACTCTCTACTTTGAAAACCGCCGACGCTCTGGAGGGGGACCTGTGTTGAGCTGGCA GAGCTGCTCACTCTCTACTTTGAAAACCGCCGGCGCTCTGGAGGGGGACCTGTGTTGAGCTGGCA T C PARP10 Ensembl:ENSG00000178685 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr8:143986063..143986387 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_Splice_Rec_1022019,Human_Splice_Rec_1022039,Human_Splice_Rec_1022057,Human_Splice_Rec_1022077,Human_Splice_Rec_1022101,Human_Splice_Rec_1022111,Human_Splice_Rec_1022117,Human_Splice_Rec_1022125,Human_Splice_Rec_1022133,Human_Splice_Rec_1022139,Human_Splice_Rec_1022145,Human_Splice_Rec_1022151,Human_Splice_Rec_1022157,Human_Splice_Rec_1022163,Human_Splice_Rec_1022171,Human_Splice_Rec_1022177,Human_Splice_Rec_1022183 RMVar_hsa_circ_2340 115694 RMVar_ID_115694 Human_SNP_ID_872850507 m1A Human chr8 - 61646853 61646850 61646853 GTCATAGTTGAGGGAGAAGACTTGCAACAAGAAGATGGACCCACAGGAGAACCACAACAAGAGGA GTCATAGTTGAGGGAGAAGACTTGCAACAAGA___TGGACCCACAGGAGAACCACAACAAGAGGA ATCT A ASPH Ensembl:ENSG00000198363 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:61646717..61646916 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 GBM 1 - Human_RBP_ID_845426,Human_RBP_ID_959849,Human_RBP_ID_5629212,Human_RBP_ID_7847497,Human_RBP_ID_9405528,Human_RBP_ID_16449311,Human_RBP_ID_26359145,Human_RBP_ID_27831920 Human_Splice_Rec_980812,Human_Splice_Rec_980858,Human_Splice_Rec_980990,Human_Splice_Rec_981014,Human_Splice_Rec_981038,Human_Splice_Rec_981086,Human_Splice_Rec_981112,Human_Splice_Rec_981192 RMVar_hsa_circ_67952,RMVar_hsa_circ_62714,RMVar_hsa_circ_372416,RMVar_hsa_circ_367068,RMVar_hsa_circ_63149,RMVar_hsa_circ_252305,RMVar_hsa_circ_66106,RMVar_hsa_circ_18929,RMVar_hsa_circ_356932,RMVar_hsa_circ_354845,RMVar_hsa_circ_323693,RMVar_hsa_circ_362181,RMVar_hsa_circ_46334,RMVar_hsa_circ_355079,RMVar_hsa_circ_366161,RMVar_hsa_circ_324201,RMVar_hsa_circ_356313,RMVar_hsa_circ_252316,RMVar_hsa_circ_309903,RMVar_hsa_circ_359967,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,RMVar_hsa_circ_322811,RMVar_hsa_circ_291764,RMVar_hsa_circ_252314,RMVar_hsa_circ_252315,RMVar_hsa_circ_326261,RMVar_hsa_circ_252313,RMVar_hsa_circ_362475,RMVar_hsa_circ_271482,RMVar_hsa_circ_252319,RMVar_hsa_circ_306904,RMVar_hsa_circ_252317,RMVar_hsa_circ_252318,RMVar_hsa_circ_311105,RMVar_hsa_circ_309039,RMVar_hsa_circ_61421,RMVar_hsa_circ_252320,RMVar_hsa_circ_252322,RMVar_hsa_circ_371589,RMVar_hsa_circ_373031,RMVar_hsa_circ_252323,RMVar_hsa_circ_75674,RMVar_hsa_circ_39855,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_47583,RMVar_hsa_circ_346654,RMVar_hsa_circ_252326,RMVar_hsa_circ_14252,RMVar_hsa_circ_252327,RMVar_hsa_circ_302003 115695 RMVar_ID_115695 Human_SNP_ID_872878599 m1A Human chr8 + 103332610 103332610 103332610 CAACGTTTTTATACAACATACTTTAAAATATTAAGGAGTTTTCTTAATTTTGTTTCCTATTAAGT CAACGTTTTTATACAACATACTTTAAAATATTGAGGAGTTTTCTTAATTTTGTTTCCTATTAAGT A G FZD6 Ensembl:ENSG00000164930 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1058130 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_692640,Human_RBP_ID_1053926,Human_RBP_ID_7794950,Human_RBP_ID_16309093,Human_RBP_ID_17544130,Human_RBP_ID_18125589,Human_RBP_ID_24518312,Human_RBP_ID_27772741 GWAS_ID_15296 115696 RMVar_ID_115696 Human_SNP_ID_872881094 m1A Human chr8 - 91070356 91070356 91070356 CCATGACGACCAGGTACCCCAGCACACGCGCTAGAAGAAACCTGCACCGGCTAGTAGGCACCTTC CCATGACGACCAGGTACCCCAGCACACGCGCTGGAAGAAACCTGCACCGGCTAGTAGGCACCTTC T C OTUD6B-AS1 Ensembl:ENSG00000253738 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:91070305..91073905 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 115697 RMVar_ID_115697 Human_SNP_ID_872885649 m1A Human chr8 + 48008469 48008469 48008469 GTCGGGCTGCAGGAGAAGATGGCGGTCTCCACAGGTCGGTTCCCGGGCCGGGCTGCGTGATTTTC GTCGGGCTGCAGGAGAAGATGGCGGTCTCCACCGGTCGGTTCCCGGGCCGGGCTGCGTGATTTTC A C UBE2V2 Ensembl:ENSG00000169139 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:48008426..48008850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_255038,Human_RBP_ID_5223650,Human_RBP_ID_16431870 Human_Splice_Rec_975853,Human_Splice_Rec_975857,Human_Splice_Rec_975865,Human_Splice_Rec_975871 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 115698 RMVar_ID_115698 Human_SNP_ID_872929138 m1A Human chr8 + 144106894 144106894 144106894 AGGCAACGAGCTGGACATGGAGCTGGGGGAGGAGGAGGTGGAGGAAGAAAGCAGAAGCGGGGGCA AGGCAACGAGCTGGACATGGAGCTGGGGGAGGTGGAGGTGGAGGAAGAAAGCAGAAGCGGGGGCA A T MAF1 Ensembl:ENSG00000179632 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr8:144106826..144106900;chr8:144106826..144106975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_7818013,Human_RBP_ID_8273961 Human_Splice_Rec_1022624,Human_Splice_Rec_1022625,Human_Splice_Rec_1022636,Human_Splice_Rec_1022637,Human_Splice_Rec_1022650,Human_Splice_Rec_1022651,Human_Splice_Rec_1022666,Human_Splice_Rec_1022668 Human_miRNA_ID_2015766 RMVar_hsa_circ_115766,RMVar_hsa_circ_255038,RMVar_hsa_circ_93211,RMVar_hsa_circ_88454,RMVar_hsa_circ_97054,RMVar_hsa_circ_255039,RMVar_hsa_circ_255040,RMVar_hsa_circ_105353,RMVar_hsa_circ_255042,RMVar_hsa_circ_255043 115699 RMVar_ID_115699 Human_SNP_ID_872967539 m1A Human chr8 - 140668302 140668302 140668302 GCTGTCATCGAGATGTCCAGTAAAATCCAGCCAGCCCCACCAGAGGAGTATGTCCCTATGGTGAA GCTGTCATCGAGATGTCCAGTAAAATCCAGCCTGCCCCACCAGAGGAGTATGTCCCTATGGTGAA T A PTK2 Ensembl:ENSG00000169398 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:140664901..140668318 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 11 lung Human_RBP_ID_9406553,Human_RBP_ID_19140371,Human_RBP_ID_26359389 Human_Splice_Rec_1015971,Human_Splice_Rec_1016031,Human_Splice_Rec_1016087,Human_Splice_Rec_1016121,Human_Splice_Rec_1016181,Human_Splice_Rec_1016243,Human_Splice_Rec_1016247,Human_Splice_Rec_1016289,Human_Splice_Rec_1016353,Human_Splice_Rec_1016417,Human_Splice_Rec_1016479,Human_Splice_Rec_1016529,Human_Splice_Rec_1016549,Human_Splice_Rec_1016595 Human_miRNA_ID_795795,Human_miRNA_ID_2331479,Human_miRNA_ID_2964562 RMVar_hsa_circ_41537,RMVar_hsa_circ_84244,RMVar_hsa_circ_101087,RMVar_hsa_circ_293999,RMVar_hsa_circ_254694,RMVar_hsa_circ_254695,RMVar_hsa_circ_320635,RMVar_hsa_circ_372352,RMVar_hsa_circ_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_254701,RMVar_hsa_circ_9428,RMVar_hsa_circ_83150,RMVar_hsa_circ_254697,RMVar_hsa_circ_254699,RMVar_hsa_circ_254700,RMVar_hsa_circ_254698,RMVar_hsa_circ_254696,RMVar_hsa_circ_287353,RMVar_hsa_circ_50766,RMVar_hsa_circ_63815,RMVar_hsa_circ_49380,RMVar_hsa_circ_6314,RMVar_hsa_circ_7623,RMVar_hsa_circ_254702 115700 RMVar_ID_115700 Human_SNP_ID_872989631 m1A Human chr8 - 144522626 144522626 144522626 CTGTACGTTCGCACAGCTAGAGGAGCTCCGCGACGAGCGCGGCCACGAGATGTTCGTCATCAACC CTGTACGTTCGCACAGCTAGAGGAGCTCCGCGCCGAGCGCGGCCACGAGATGTTCGTCATCAACC T G LRRC24 Ensembl:ENSG00000254402 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144522576..144522749 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 3 breast RMVar_hsa_circ_255171 115701 RMVar_ID_115701 Human_SNP_ID_873023577 m1A Human chr8 - 54135296 54135296 54135296 TAGGTCCAGGGCCCGGGCCCCACCGCCCTGCAAGGGACCGGCCATAACCCGCAGATCCAAGAACT TAGGTCCAGGGCCCGGGCCCCACCGCCCTGCACGGGACCGGCCATAACCCGCAGATCCAAGAACT T G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:54135201..54136597 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115702 RMVar_ID_115702 Human_SNP_ID_873094501 m1A Human chr8 - 142300586 142300586 142300586 GGCTGATGATGAGAAGGTCTTTAACGGGAGTGACAACATGTGGCAGGGCCAGGAGCAGGCGCTGC GGCTGATGATGAGAAGGTCTTTAACGGGAGTGGCAACATGTGGCAGGGCCAGGAGCAGGCGCTGC T C TSNARE1 Ensembl:ENSG00000171045 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:142300398..142300599 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19023089 Human_Splice_Rec_1017606,Human_Splice_Rec_1017632,Human_Splice_Rec_1017656,Human_Splice_Rec_1017678,Human_Splice_Rec_1017704,Human_Splice_Rec_1017718 RMVar_hsa_circ_328,RMVar_hsa_circ_85726,RMVar_hsa_circ_102029,RMVar_hsa_circ_254850,RMVar_hsa_circ_20984,RMVar_hsa_circ_38101,RMVar_hsa_circ_93509,RMVar_hsa_circ_375628,RMVar_hsa_circ_254851,RMVar_hsa_circ_254852,RMVar_hsa_circ_43441,RMVar_hsa_circ_8446,RMVar_hsa_circ_41022,RMVar_hsa_circ_322207,RMVar_hsa_circ_254853,RMVar_hsa_circ_323268,RMVar_hsa_circ_310848,RMVar_hsa_circ_254854 115703 RMVar_ID_115703 Human_SNP_ID_873102191 m1A Human chr8 - 140585264 140585264 140585264 CGCCGCCGCCCCCCATCCAAGGATATGCCTTCAAGCCTCCACCTAGACCCGACTTTGGGACCTCC CGCCGCCGCCCCCCATCCAAGGATATGCCTTCCAGCCTCCACCTAGACCCGACTTTGGGACCTCC T G AGO2 Ensembl:ENSG00000123908 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:140585226..140585275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_2053176,Human_RBP_ID_3973353,Human_RBP_ID_4972147,Human_RBP_ID_9338382,Human_RBP_ID_18892694,Human_RBP_ID_22115179 Human_Splice_Rec_1015792,Human_Splice_Rec_1015826,Human_Splice_Rec_1015902,Human_Splice_Rec_1015908 Human_miRNA_ID_2931813 RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_254673,RMVar_hsa_circ_358666,RMVar_hsa_circ_254675,RMVar_hsa_circ_301532,RMVar_hsa_circ_374147,RMVar_hsa_circ_79763,RMVar_hsa_circ_254677,RMVar_hsa_circ_254680,RMVar_hsa_circ_329497,RMVar_hsa_circ_254681,RMVar_hsa_circ_343450,RMVar_hsa_circ_254685,RMVar_hsa_circ_254686,RMVar_hsa_circ_82751,RMVar_hsa_circ_370770,RMVar_hsa_circ_327307,RMVar_hsa_circ_254687,RMVar_hsa_circ_76427,RMVar_hsa_circ_254688,RMVar_hsa_circ_309313,RMVar_hsa_circ_254690,RMVar_hsa_circ_276809,RMVar_hsa_circ_254689,RMVar_hsa_circ_300236,RMVar_hsa_circ_254691,RMVar_hsa_circ_254692 115704 RMVar_ID_115704 Human_SNP_ID_873129393 m1A Human chr8 - 85107315 85107315 85107315 CTTCGTTTTCCACTTCCGCCTCTGCCGCCACCACCGCCGCCGCCGCCTCCATAGCACTGGCGACG CTTCGTTTTCCACTTCCGCCTCTGCCGCCACCGCCGCCGCCGCCGCCTCCATAGCACTGGCGACG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:85107269..85107353 26863196 MeRIP-seq:(Medium) rs749120809 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,large_intestine adenocarcinoma 3 large intestine 115705 RMVar_ID_115705 Human_SNP_ID_873143823 m1A Human chr8 - 127740699 127740699 127740699 GGCGCTCCAAGACGTTGTGTGTTCGCCTCTTGACATTCTCCTCGGTGTCCGAGGACCTGGGGCTG GGCGCTCCAAGACGTTGTGTGTTCGCCTCTTGTCATTCTCCTCGGTGTCCGAGGACCTGGGGCTG T A lnc-FAM84B-20 RNACentral:URS0000D5E1FC lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:127740371..127741000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 115706 RMVar_ID_115706 Human_SNP_ID_873151192 m1A Human chr8 - 143922240 143922240 143922240 GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCACAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA GAGCAGCTCTTCCAGGACGAGGTGGCCAAGGCCCAGCAGCTGCGTGAGGAGCAGCAGCGGCAGCA T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143921726..143922300 26863196 MeRIP-seq:(Medium) rs11778026 Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 22 kidney,large intestine Human_RBP_ID_89147,Human_RBP_ID_5154354,Human_RBP_ID_5534402,Human_RBP_ID_18472624,Human_RBP_ID_24549426,Human_RBP_ID_26359469 GWAS_ID_7884 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 115707 RMVar_ID_115707 Human_SNP_ID_873168925 m1A Human chr8 - 30703126 30703126 30703126 CCGCCCCACACATCCTGATCGCCACAGGTGGTATGCCCTCCACCCCTCATGAGAGCCAGATCCCC CCGCCCCACACATCCTGATCGCCACAGGTGGTGTGCCCTCCACCCCTCATGAGAGCCAGATCCCC T C GSR Ensembl:ENSG00000104687 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:30703094..30708075 32194978 MeRIP-seq:(Medium) rs758849140 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,STAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_795516,Human_RBP_ID_4982771,Human_RBP_ID_18196718,Human_RBP_ID_26832645 Human_Splice_Rec_963591,Human_Splice_Rec_963617,Human_Splice_Rec_963643,Human_Splice_Rec_963667,Human_Splice_Rec_963687,Human_Splice_Rec_963709,Human_Splice_Rec_963747 Human_miRNA_ID_2153197,Human_miRNA_ID_2695517,Human_miRNA_ID_2801071,Human_miRNA_ID_3009199 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_277103,RMVar_hsa_circ_251112,RMVar_hsa_circ_99877,RMVar_hsa_circ_316740,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_349314,RMVar_hsa_circ_251113,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_352903,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251121,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_338456,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_251127,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_276969,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_102640,RMVar_hsa_circ_378637,RMVar_hsa_circ_251128 115708 RMVar_ID_115708 Human_SNP_ID_873174457 m1A Human chr8 - 98774817 98774817 98774817 ATTTTCTTTCTTCTTTCTTTTTTAAATCAGTAAACTAAAAAAGCTGAGTGAAGACAGTTTGACTA ATTTTCTTTCTTCTTTCTTTTTTAAATCAGTACACTAAAAAAGCTGAGTGAAGACAGTTTGACTA T G STK3 Ensembl:ENSG00000104375 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98774796..98774866 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_27832024 Human_Splice_Rec_996120,Human_Splice_Rec_996121,Human_Splice_Rec_996136,Human_Splice_Rec_996137,Human_Splice_Rec_996160,Human_Splice_Rec_996161,Human_Splice_Rec_996194,Human_Splice_Rec_996195,Human_Splice_Rec_996214,Human_Splice_Rec_996215,Human_Splice_Rec_996236,Human_Splice_Rec_996237 RMVar_hsa_circ_124809,RMVar_hsa_circ_253358,RMVar_hsa_circ_76036,RMVar_hsa_circ_97793,RMVar_hsa_circ_253369,RMVar_hsa_circ_74314,RMVar_hsa_circ_289442,RMVar_hsa_circ_253378,RMVar_hsa_circ_253379,RMVar_hsa_circ_266366,RMVar_hsa_circ_359450,RMVar_hsa_circ_332792,RMVar_hsa_circ_253382,RMVar_hsa_circ_300856 115709 RMVar_ID_115709 Human_SNP_ID_873197223 m1A Human chr8 - 22138476 22138476 22138476 GCCCTCAGACGTGGACAGCTAGGGTCTGCTGCATCTGCCCCCTTCTTACCTCGTGCCCTGCAGGG GCCCTCAGACGTGGACAGCTAGGGTCTGCTGCGTCTGCCCCCTTCTTACCTCGTGCCCTGCAGGG T C REEP4 Ensembl:ENSG00000168476 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22138427..22138548 26863196 MeRIP-seq:(Medium) rs753161492 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_697123,Human_RBP_ID_1694943,Human_RBP_ID_5123844,Human_RBP_ID_5154228,Human_RBP_ID_7823588,Human_RBP_ID_17665935,Human_RBP_ID_18115511,Human_RBP_ID_22516869,Human_RBP_ID_24252890 Human_Splice_Rec_955938,Human_Splice_Rec_955952,Human_Splice_Rec_955964 Human_miRNA_ID_2384400 RMVar_hsa_circ_76069,RMVar_hsa_circ_250695 115710 RMVar_ID_115710 Human_SNP_ID_873208291 m1A Human chr8 - 143975260 143975232 143975260 GGACACACTGCCCTGGAACCTTGGGAAAACGCAGCGGAGCCGGCGCAGCGGGGGTGGCGCTGGGA GGACACACTGCCCTGGAACCTTGGGAAAACGC____________________________TGGGA AGCGCCACCCCCGCTGCGCCGGCTCCGCT A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143975228..143975627 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..60 33 READ 1 - Human_RBP_ID_4974492 Human_Splice_Rec_1021761,Human_Splice_Rec_1021821,Human_Splice_Rec_1021879,Human_Splice_Rec_1021939,Human_Splice_Rec_1022005 115711 RMVar_ID_115711 Human_SNP_ID_873224662 m1A Human chr8 - 143934384 143934382 143934385 GCCCCCTGGCTACCACCCGCTGGATGTGGAGAAGGAGTGGGGCAAGCTGCACGTGGCCATCCTGG GCCCCCTGGCTACCACCCGCTGGATGTGGAG___GAGTGGGGCAAGCTGCACGTGGCCATCCTGG CCTT C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143934376..143934400 26863196 MeRIP-seq:(Medium) rs782613887 Functional Loss DEL TCGA,ICGC 32..34 33 COAD,SKCM 2 - Human_RBP_ID_22465038 Human_Splice_Rec_1021360,Human_Splice_Rec_1021361,Human_Splice_Rec_1021420,Human_Splice_Rec_1021421,Human_Splice_Rec_1021480,Human_Splice_Rec_1021481,Human_Splice_Rec_1021540,Human_Splice_Rec_1021541,Human_Splice_Rec_1021600,Human_Splice_Rec_1021601,Human_Splice_Rec_1021660,Human_Splice_Rec_1021661,Human_Splice_Rec_1021720,Human_Splice_Rec_1021721,Human_Splice_Rec_1021780,Human_Splice_Rec_1021781,Human_Splice_Rec_1021840,Human_Splice_Rec_1021841,Human_Splice_Rec_1021898,Human_Splice_Rec_1021899,Human_Splice_Rec_1021962,Human_Splice_Rec_1021963 Human_miRNA_ID_207166,Human_miRNA_ID_1490935,Human_miRNA_ID_2012517,Human_miRNA_ID_2012518,Human_miRNA_ID_2708427,Human_miRNA_ID_2708428,Human_miRNA_ID_2758893,Human_miRNA_ID_2758894 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_85553,RMVar_hsa_circ_3035,RMVar_hsa_circ_254972,RMVar_hsa_circ_254974,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985,RMVar_hsa_circ_99232,RMVar_hsa_circ_121074,RMVar_hsa_circ_254988,RMVar_hsa_circ_254987,RMVar_hsa_circ_10998,RMVar_hsa_circ_57497,RMVar_hsa_circ_108803,RMVar_hsa_circ_108144,RMVar_hsa_circ_254989,RMVar_hsa_circ_254991,RMVar_hsa_circ_96142,RMVar_hsa_circ_254990 115712 RMVar_ID_115712 Human_SNP_ID_873309770 m1A Human chr8 + 11200945 11200945 11200945 CGTCCCCGAAGAACACCAGCAGCGCCAGCACGATCCACAGGCAGTCGAGCCACGGCCGCTCCACC CGTCCCCGAAGAACACCAGCAGCGCCAGCACGGTCCACAGGCAGTCGAGCCACGGCCGCTCCACC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:11200902..11201017 32194978 MeRIP-seq:(Medium) rs1314352640 Functional Loss SNV TCGA 33..33 33 PRAD 1 - 115713 RMVar_ID_115713 Human_SNP_ID_873330203 m1A Human chr8 - 144519798 144519798 144519798 GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCAAGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT GAACAGCAGGGGGAAGAGTTCGCGTGGCAGCAGGGGCAGGGCCTGGCAGGCAGCTGGCTGGCACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144519749..144519834 26863196 MeRIP-seq:(Medium) rs2721172 Functional Loss SNV COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,thyroid neoplasm,central_nervous_system oligodendroglioma_Grade_II 4 head and neck,brain 115714 RMVar_ID_115714 Human_SNP_ID_873397518 m1A Human chr8 - 22617511 22617511 22617511 CCCTCAGAAGCAACAGTTCTGGGTCCAGGGCCATCTCACACAGGTCCTCAGAAGCCTCGCCCCGG CCCTCAGAAGCAACAGTTCTGGGTCCAGGGCCCTCTCACACAGGTCCTCAGAAGCCTCGCCCCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22617401..22617575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 6 brain 115715 RMVar_ID_115715 Human_SNP_ID_873398740 m1A Human chr8 - 41933198 41933198 41933198 CCACAACCACAACCAGCACCACAGCCTCCACCACCCCAGCAGCAGCCGCAACAGCAGCCGCAGCC CCACAACCACAACCAGCACCACAGCCTCCACCTCCCCAGCAGCAGCCGCAACAGCAGCCGCAGCC T A KAT6A Ensembl:ENSG00000083168 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:41933147..41933293 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - Human_RBP_ID_89647,Human_RBP_ID_17320012 RMVar_hsa_circ_264802 115716 RMVar_ID_115716 Human_SNP_ID_873424967 m1A Human chr8 + 142489428 142489428 142489428 CCTGCGCACACCCTTGGAGATCGAGTTTGCCCACATGTATAATGTGAGTGCCGTCCACGTGCACA CCTGCGCACACCCTTGGAGATCGAGTTTGCCCGCATGTATAATGTGAGTGCCGTCCACGTGCACA A G ADGRB1 Ensembl:ENSG00000181790 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142481708..142518193 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1017762,Human_Splice_Rec_1017763,Human_Splice_Rec_1017820,Human_Splice_Rec_1017821,Human_Splice_Rec_1017878,Human_Splice_Rec_1017879,Human_Splice_Rec_1017932,Human_Splice_Rec_1017933,Human_Splice_Rec_1017976,Human_Splice_Rec_1017977 RMVar_hsa_circ_80964,RMVar_hsa_circ_47972,RMVar_hsa_circ_254863,RMVar_hsa_circ_265644 115717 RMVar_ID_115717 Human_SNP_ID_873465379 m1A Human chr8 - 143614436 143614436 143614436 GCTGTGCCTCCGCAGGGCCTACTTCCAGCAGTACGGCTGCACCTTCACCGCTGTCATCCCCACCA GCTGTGCCTCCGCAGGGCCTACTTCCAGCAGTGCGGCTGCACCTTCACCGCTGTCATCCCCACCA T C TSTA3 Ensembl:ENSG00000104522 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143614385..143614639 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_3973392,Human_RBP_ID_18172682,Human_RBP_ID_27832196 Human_Splice_Rec_1019994,Human_Splice_Rec_1020030,Human_Splice_Rec_1020052,Human_Splice_Rec_1020080,Human_Splice_Rec_1020090 Human_miRNA_ID_2143435,Human_miRNA_ID_2144967,Human_miRNA_ID_2687470 RMVar_hsa_circ_85140,RMVar_hsa_circ_96168,RMVar_hsa_circ_101597,RMVar_hsa_circ_254914,RMVar_hsa_circ_254915,RMVar_hsa_circ_254916 115718 RMVar_ID_115718 Human_SNP_ID_873479123 m1A Human chr8 - 22620299 22620299 22620299 AGAGCCAATACCACATTCTGAACACAGGAGCCACGGGAAAGAGGTGCTGGTTTCTTCTGGCAAGA AGAGCCAATACCACATTCTGAACACAGGAGCCGCGGGAAAGAGGTGCTGGTTTCTTCTGGCAAGA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:22620251..22620325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 115719 RMVar_ID_115719 Human_SNP_ID_873534786 m1A Human chr8 - 23309815 23309815 23309815 CATGTTCATGCTGCAGTGTGCCATGGAGGAGAACTGCCTCTCGGCCTCAGCCGCGCAGACCGACC CATGTTCATGCTGCAGTGTGCCATGGAGGAGAGCTGCCTCTCGGCCTCAGCCGCGCAGACCGACC T C LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:23309764..23309962 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 2 uterus Human_Splice_Rec_958488 Human_miRNA_ID_2279605,Human_miRNA_ID_2459666,Human_miRNA_ID_2639898 RMVar_hsa_circ_11094,RMVar_hsa_circ_45914,RMVar_hsa_circ_28168,RMVar_hsa_circ_53278,RMVar_hsa_circ_250782,RMVar_hsa_circ_109885,RMVar_hsa_circ_331761,RMVar_hsa_circ_343155,RMVar_hsa_circ_348092,RMVar_hsa_circ_118425,RMVar_hsa_circ_250783 115720 RMVar_ID_115720 Human_SNP_ID_873574986 m1A Human chr8 - 30095467 30095467 30095467 CTCCTGGCTCCACGACCCGAGGCGGCGGCGGCAGCAGCGGCAGCCGGGAGACCCAAGACGCGCTA CTCCTGGCTCCACGACCCGAGGCGGCGGCGGCGGCAGCGGCAGCCGGGAGACCCAAGACGCGCTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:30095426..30095550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115721 RMVar_ID_115721 Human_SNP_ID_873579956 m1A Human chr8 + 19939318 19939318 19939318 AGGGAAAGCTGCCCACTTCTAGCTGCCCTGCCATCCCCTTTAAAGGGCGACTTGCTCAGCGCCAA AGGGAAAGCTGCCCACTTCTAGCTGCCCTGCCTTCCCCTTTAAAGGGCGACTTGCTCAGCGCCAA A T LPL Ensembl:ENSG00000175445 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:19939251..19939567 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_Splice_Rec_954312,Human_Splice_Rec_954318 115722 RMVar_ID_115722 Human_SNP_ID_873597306 m1A Human chr8 - 18084914 18084914 18084914 CACCTACCCGCGCGACTGTGTCCACGGATGGCACGAAAGCCAAGCGAGTCCCCCTGCCGAGCTAC CACCTACCCGCGCGACTGTGTCCACGGATGGCCCGAAAGCCAAGCGAGTCCCCCTGCCGAGCTAC T G ASAH1 Ensembl:ENSG00000104763 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:18084819..18084938 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 CESC 1 - 115723 RMVar_ID_115723 Human_SNP_ID_873606861 m1A Human chr8 + 123811694 123811694 123811694 GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCAATGATGGGCATACTGAGTATAGAGTGCATGGGG GAGGAAGAGGGGAGGGAAAATTTGAGAGTTCATTGATGGGCATACTGAGTATAGAGTGCATGGGG A T FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:123811648..123811811 26863196 MeRIP-seq:(Medium) rs150629850 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_9338708,Human_RBP_ID_16343243,Human_RBP_ID_22484254,Human_RBP_ID_24244439 RMVar_hsa_circ_91949,RMVar_hsa_circ_254225,RMVar_hsa_circ_108974,RMVar_hsa_circ_254231 115724 RMVar_ID_115724 Human_SNP_ID_873607062 m1A Human chr8 - 143572728 143572728 143572728 AACTTCGCAGGAGGAGCAGCGGCAGGTGCTGCAGGCAAGGGCCGCCATGGCTGGGGGTGTGTGGG AACTTCGCAGGAGGAGCAGCGGCAGGTGCTGCCGGCAAGGGCCGCCATGGCTGGGGGTGTGTGGG T G MROH6 Ensembl:ENSG00000204839 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143572635..143572880 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_958600 115725 RMVar_ID_115725 Human_SNP_ID_873631633 m1A Human chr8 + 108214698 108214698 108214698 TTCAATGAAATCCTCAAGACAAGCCACCAAGAAGAAGTCATTCACAAGCACCTATATGTACAAAT TTCAATGAAATCCTCAAGACAAGCCACCAAGAGGAAGTCATTCACAAGCACCTATATGTACAAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:108214626..108214725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cervix small_cell_carcinoma 2 uterus 115726 RMVar_ID_115726 Human_SNP_ID_873639984 m1A Human chr8 + 8328033 8328033 8328033 ACTGGACACGCTCAGCTGGGAGGATGAGGCGGAGGGGGCCCCTTTGCACTGGAGGCCAGGGCTCC ACTGGACACGCTCAGCTGGGAGGATGAGGCGGGGGGGGCCCCTTTGCACTGGAGGCCAGGGCTCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8327986..8328071 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115727 RMVar_ID_115727 Human_SNP_ID_873658361 m1A Human chr8 + 38234513 38234513 38234513 GGGATGAACTGGCATCGGAAGTGAGACGATGTACGTGGTTTTACAAGGGGGACAAAGACAATAAG GGGATGAACTGGCATCGGAAGTGAGACGATGTGCGTGGTTTTACAAGGGGGACAAAGACAATAAG A G DDHD2 Ensembl:ENSG00000085788 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:38234463..38238277 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_699223,Human_RBP_ID_9313383,Human_RBP_ID_9405342,Human_RBP_ID_24257170,Human_RBP_ID_26832674 Human_Splice_Rec_966199,Human_Splice_Rec_966209,Human_Splice_Rec_966243,Human_Splice_Rec_966265,Human_Splice_Rec_966271,Human_Splice_Rec_966277,Human_Splice_Rec_966287,Human_Splice_Rec_966319 RMVar_hsa_circ_19263,RMVar_hsa_circ_127338,RMVar_hsa_circ_357349,RMVar_hsa_circ_367371,RMVar_hsa_circ_343422,RMVar_hsa_circ_64088,RMVar_hsa_circ_251367,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_251366,RMVar_hsa_circ_328935,RMVar_hsa_circ_49606,RMVar_hsa_circ_251368 115728 RMVar_ID_115728 Human_SNP_ID_873661175 m1A Human chr8 - 27658775 27658775 27658775 ACTCCTGGGTGAGGTCCTTCAGAGAGAGGTCCAGGCCAGCTGTGGTGGCCTGCCAGCCTCTCACC ACTCCTGGGTGAGGTCCTTCAGAGAGAGGTCCCGGCCAGCTGTGGTGGCCTGCCAGCCTCTCACC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:27658583..27658883 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 115729 RMVar_ID_115729 Human_SNP_ID_873691220 m1A Human chr8 - 143932923 143932923 143932923 GCAGGACCTGCTGGCCTGGGTGGAGGAGAACCAGCACCGTGTGGATGGCGCTGAGTGGGGTGTGG GCAGGACCTGCTGGCCTGGGTGGAGGAGAACCCGCACCGTGTGGATGGCGCTGAGTGGGGTGTGG T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143932792..143933138 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_105904,RMVar_hsa_circ_85553,RMVar_hsa_circ_254972,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982,RMVar_hsa_circ_99763,RMVar_hsa_circ_254984,RMVar_hsa_circ_22489,RMVar_hsa_circ_124799,RMVar_hsa_circ_254986,RMVar_hsa_circ_97918,RMVar_hsa_circ_254985,RMVar_hsa_circ_99232,RMVar_hsa_circ_121074,RMVar_hsa_circ_254988,RMVar_hsa_circ_54722,RMVar_hsa_circ_254987 115730 RMVar_ID_115730 Human_SNP_ID_873702762 m1A Human chr8 + 73746349 73746349 73746349 TACTCTAGGCGCTCCCTCTCCCTCGCAGCCACACCGTGGCTGCACTCGCCGTCCTCTCTTCCGGC TACTCTAGGCGCTCCCTCTCCCTCGCAGCCACCCCGTGGCTGCACTCGCCGTCCTCTCTTCCGGC A C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:73746253..73746446 26863196 MeRIP-seq:(Medium) rs1224211180 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115731 RMVar_ID_115731 Human_SNP_ID_873711528 m1A Human chr8 - 144096736 144096736 144096736 ACTGCCAGACTGGAGGCCTCTTACCATCGTCAAACTCTAAGACATCTGTGTAGATGGGAGGGGCC ACTGCCAGACTGGAGGCCTCTTACCATCGTCACACTCTAAGACATCTGTGTAGATGGGAGGGGCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:144096726..144096750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 2 stomach 115732 RMVar_ID_115732 Human_SNP_ID_873724935 m1A Human chr8 - 116644963 116644963 116644963 TTTCCAGAAAAGAAGTTAACATGAACTCTTGAAGTCACACCAGGGCAACTCTTGGAAGAAATATA TTTCCAGAAAAGAAGTTAACATGAACTCTTGACGTCACACCAGGGCAACTCTTGGAAGAAATATA T G EIF3H Ensembl:ENSG00000147677 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_89851,Human_RBP_ID_693424,Human_RBP_ID_1054134,Human_RBP_ID_1692624,Human_RBP_ID_2051854,Human_RBP_ID_3871536,Human_RBP_ID_8678228,Human_RBP_ID_9220095,Human_RBP_ID_16324652,Human_RBP_ID_17316952,Human_RBP_ID_17431732,Human_RBP_ID_17544263,Human_RBP_ID_18890567,Human_RBP_ID_21953385,Human_RBP_ID_23216184,Human_RBP_ID_26832361,Human_RBP_ID_27535471,Human_RBP_ID_27773430 Human_miRNA_ID_252444,Human_miRNA_ID_861754,Human_miRNA_ID_1465060 115733 RMVar_ID_115733 Human_SNP_ID_873765838 m1A Human chr8 + 25410106 25410106 25410106 CGCCTGCACTTTCTGTCATTTCTAGGCTCCCCATCGTTGCAGACAGATGGAATCGCGGCCACTCC CGCCTGCACTTTCTGTCATTTCTAGGCTCCCCGTCGTTGCAGACAGATGGAATCGCGGCCACTCC A G DOCK5 Ensembl:ENSG00000147459 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:25410101..25410209 26863196 MeRIP-seq:(Medium) rs2709618 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 13 head and neck,large intestine,haematopoietic and lymphoid tissue,breast Human_RBP_ID_19140965 Human_Splice_Rec_959370,Human_Splice_Rec_959371,Human_Splice_Rec_959528,Human_Splice_Rec_959529,Human_Splice_Rec_959541,Human_Splice_Rec_959543 GWAS_ID_13112,GWAS_ID_13113,GWAS_ID_13114 RMVar_hsa_circ_265906,RMVar_hsa_circ_26083,RMVar_hsa_circ_250869,RMVar_hsa_circ_344705 115734 RMVar_ID_115734 Human_SNP_ID_873808260 m1A Human chr8 + 124451019 124451019 124451019 TGTCGCAGTTGTGACTGAGCCTTGGTTTACCCAGCGATACAGAGAATATCTCCAGAGGCAGAAAC TGTCGCAGTTGTGACTGAGCCTTGGTTTACCCTGCGATACAGAGAATATCTCCAGAGGCAGAAAC A T TRMT12 Ensembl:ENSG00000183665 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:124450918..124451018 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_1693203,Human_RBP_ID_2052638,Human_RBP_ID_18891695 115735 RMVar_ID_115735 Human_SNP_ID_873809717 m1A Human chr8 - 123014660 123014660 123014660 GAGTTGCAGCTAACATGGGTTAGGTTTAAACCATGGGGGATGCAACCCCTTTGCGTTTCATATGT GAGTTGCAGCTAACATGGGTTAGGTTTAAACCGTGGGGGATGCAACCCCTTTGCGTTTCATATGT T C DERL1 Ensembl:ENSG00000136986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:123014609..123014710 32194978 MeRIP-seq:(Medium) rs1059588 Functional Loss SNV ICGC 33..33 33 ESCA 2 - GWAS_ID_8728,GWAS_ID_8729,GWAS_ID_8730 115736 RMVar_ID_115736 Human_SNP_ID_873816400 m1A Human chr8 - 11802853 11802853 11802853 CGCACCAGGTTGTAGAACTCTTCGGGGTGGCCAAGGCATTTCACGAACTCCATCCTGGCGCAGGC CGCACCAGGTTGTAGAACTCTTCGGGGTGGCCGAGGCATTTCACGAACTCCATCCTGGCGCAGGC T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:11802751..11802925 26863410 MeRIP-seq:(Medium) rs1047643 Functional Loss SNV ICGC 33..33 33 LUSC 1 - GWAS_ID_13422,GWAS_ID_13423 115737 RMVar_ID_115737 Human_SNP_ID_873817728 m1A Human chr8 - 42342344 42342344 42342344 GTGTGAAGGTTGGCCTGACAAATTATGCTGCAACATATTGTACTGGCCTGCTGCTGGCCCACAGG GTGTGAAGGTTGGCCTGACAAATTATGCTGCAGCATATTGTACTGGCCTGCTGCTGGCCCACAGG T C RPL5P23 Ensembl:ENSG00000240395 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879032377 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_miRNA_ID_1830899,Human_miRNA_ID_1836339,Human_miRNA_ID_1841465,Human_miRNA_ID_1862958,Human_miRNA_ID_1878738,Human_miRNA_ID_1882892,Human_miRNA_ID_1908692,Human_miRNA_ID_1909253 115738 RMVar_ID_115738 Human_SNP_ID_873832854 m1A Human chr8 + 66612996 66612996 66612996 GCGGAACGCACGTCCTCGACAGGGCAGGACGGAGGGACAGCGGGGGCGGACCGCGACCCGACCCC GCGGAACGCACGTCCTCGACAGGGCAGGACGGGGGGACAGCGGGGGCGGACCGCGACCCGACCCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:66612948..66613240 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 115739 RMVar_ID_115739 Human_SNP_ID_873835883 m1A Human chr8 + 143684516 143684516 143684516 AGTCTGGGCTACCGGCGCGGCGTAGTGGATGCAGCATCCTAGTGGAGGACGCCCCTGTGGTGAGT AGTCTGGGCTACCGGCGCGGCGTAGTGGATGCTGCATCCTAGTGGAGGACGCCCCTGTGGTGAGT A T ZNF707 Ensembl:ENSG00000181135 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143684513..143684596 26863196 MeRIP-seq:(Medium) rs62524205 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1020123,Human_Splice_Rec_1020127,Human_Splice_Rec_1020135,Human_Splice_Rec_1020143,Human_Splice_Rec_1020151,Human_Splice_Rec_1020153,Human_Splice_Rec_1020163,Human_Splice_Rec_1020173,Human_Splice_Rec_1020181,Human_Splice_Rec_1020191,Human_Splice_Rec_1020201,Human_Splice_Rec_1020211,Human_Splice_Rec_1020217,Human_Splice_Rec_1020227,Human_Splice_Rec_1020235,Human_Splice_Rec_1020243,Human_Splice_Rec_1020251,Human_Splice_Rec_1020255,Human_Splice_Rec_1020261,Human_Splice_Rec_1020267,Human_Splice_Rec_1020279,Human_Splice_Rec_1020285,Human_Splice_Rec_1020297,Human_Splice_Rec_1020303,Human_Splice_Rec_1020315 115740 RMVar_ID_115740 Human_SNP_ID_873867857 m1A Human chr8 + 123142406 123142406 123142406 AGGAAGTAGCCAAACTCCTTAGGGAAAACAGAAGGAAAGAAATAGAGATAATAAATGCAATGGTG AGGAAGTAGCCAAACTCCTTAGGGAAAACAGACGGAAAGAAATAGAGATAATAAATGCAATGGTG A C TBC1D31 Ensembl:ENSG00000156787 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:123142357..123142492 26863196 MeRIP-seq:(Medium) rs141224192 Functional Loss SNV COSMIC 33..33 33 meninges fibroblastic 5 brain Human_Splice_Rec_1005097,Human_Splice_Rec_1005175,Human_Splice_Rec_1005227,Human_Splice_Rec_1005321 RMVar_hsa_circ_338515,RMVar_hsa_circ_297281,RMVar_hsa_circ_298414,RMVar_hsa_circ_254138,RMVar_hsa_circ_254136,RMVar_hsa_circ_254137,RMVar_hsa_circ_42520,RMVar_hsa_circ_254163,RMVar_hsa_circ_54817,RMVar_hsa_circ_341130,RMVar_hsa_circ_319544,RMVar_hsa_circ_320179,RMVar_hsa_circ_254164,RMVar_hsa_circ_254165,RMVar_hsa_circ_376931,RMVar_hsa_circ_66904,RMVar_hsa_circ_254166,RMVar_hsa_circ_64145,RMVar_hsa_circ_56825,RMVar_hsa_circ_64996,RMVar_hsa_circ_317901,RMVar_hsa_circ_254168,RMVar_hsa_circ_292899,RMVar_hsa_circ_254167,RMVar_hsa_circ_318559,RMVar_hsa_circ_254169 115741 RMVar_ID_115741 Human_SNP_ID_873874550 m1A Human chr8 - 144401501 144401501 144401501 TTGCTGCCTCCTTCTCCTTCTTTGGCAACGTCATGTCCATGGCCAGCGTGCAGCTGGCAGGAGCC TTGCTGCCTCCTTCTCCTTCTTTGGCAACGTCGTGTCCATGGCCAGCGTGCAGCTGGCAGGAGCC T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144401476..144401500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_18893597 Human_Splice_Rec_1023972,Human_Splice_Rec_1023973,Human_Splice_Rec_1024044,Human_Splice_Rec_1024045,Human_Splice_Rec_1024134,Human_Splice_Rec_1024135,Human_Splice_Rec_1024162,Human_Splice_Rec_1024163 Human_miRNA_ID_2393001 115742 RMVar_ID_115742 Human_SNP_ID_873880338 m1A Human chr8 - 63038671 63038671 63038671 GCTGTCTAGACCCCACGGCGACACCGCCAAGAAGCCCATCATCGGTAAGGAGGCTGTGCGGGGCC GCTGTCTAGACCCCACGGCGACACCGCCAAGATGCCCATCATCGGTAAGGAGGCTGTGCGGGGCC T A GGH Ensembl:ENSG00000137563 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:63038651..63038700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate Human_RBP_ID_796596,Human_RBP_ID_4995543,Human_RBP_ID_19140212,Human_RBP_ID_27126166 Human_Splice_Rec_981357,Human_Splice_Rec_981375,Human_Splice_Rec_981397,Human_Splice_Rec_981403 115743 RMVar_ID_115743 Human_SNP_ID_873903828 m1A Human chr8 + 143917364 143917364 143917364 AATCAGGCCCTTGCGGTAGGCCTCGTACACTGACATCTCCTTGCCCGTCTCGGGGTCCACGATGA AATCAGGCCCTTGCGGTAGGCCTCGTACACTGGCATCTCCTTGCCCGTCTCGGGGTCCACGATGA A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143917315..143917902 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 115744 RMVar_ID_115744 Human_SNP_ID_873904637 m1A Human chr8 + 140120636 140120633 140120637 TCCAACATCCATCCATCCGTCCAACATCCAACATCCATCCATCCATCCATTCATCCATCCACCCA TCCAACATCCATCCATCCGTCCAACATCCA____CCATCCATCCATCCATTCATCCATCCACCCA AACAT A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140120614..140120800 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 LMS 1 - 115745 RMVar_ID_115745 Human_SNP_ID_874009369 m1A Human chr8 - 65682448 65682448 65682448 AAATACTTAAAATATATAAAATATAATACCTGAAACTGAACTCTTGGACACTGAATCAGAGACAA AAATACTTAAAATATATAAAATATAATACCTGCAACTGAACTCTTGGACACTGAATCAGAGACAA T G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:65682441..65704882 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 115746 RMVar_ID_115746 Human_SNP_ID_874082252 m1A Human chr8 + 1839785 1839785 1839785 GCTGTCTGGTGTGGGGACTGTCTGGTGTGGGTACTGTCTGGTGTGGGGACTGTCTTGTGTGGAAG GCTGTCTGGTGTGGGGACTGTCTGGTGTGGGTGCTGTCTGGTGTGGGGACTGTCTTGTGTGGAAG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:1839766..1839902 26863196 MeRIP-seq:(Medium) rs1396318428 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_5657993,Human_RBP_ID_27843264 RMVar_hsa_circ_346810 115747 RMVar_ID_115747 Human_SNP_ID_874108367 m1A Human chr8 - 100706794 100706794 100706794 CAAAATGTTCTTATTTTTTAGCTAACACATCAACACAGACAATGGGTCCACGTCCTGCAGCTGCA CAAAATGTTCTTATTTTTTAGCTAACACATCAGCACAGACAATGGGTCCACGTCCTGCAGCTGCA T C PABPC1 Ensembl:ENSG00000070756 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_87910,Human_RBP_ID_960508,Human_RBP_ID_1053823,Human_RBP_ID_1691724,Human_RBP_ID_2050663,Human_RBP_ID_8676352,Human_RBP_ID_17316757,Human_RBP_ID_17431535,Human_RBP_ID_17543915,Human_RBP_ID_18386208,Human_RBP_ID_18889169,Human_RBP_ID_27535147 Human_Splice_Rec_997584,Human_Splice_Rec_997612,Human_Splice_Rec_997642,Human_Splice_Rec_997672,Human_Splice_Rec_997702,Human_Splice_Rec_997730,Human_Splice_Rec_997742,Human_Splice_Rec_997758 Human_miRNA_ID_2986717 RMVar_hsa_circ_17325,RMVar_hsa_circ_89246,RMVar_hsa_circ_253523,RMVar_hsa_circ_310376,RMVar_hsa_circ_327546,RMVar_hsa_circ_373272,RMVar_hsa_circ_345555,RMVar_hsa_circ_313470,RMVar_hsa_circ_306988,RMVar_hsa_circ_116480,RMVar_hsa_circ_60384,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253527,RMVar_hsa_circ_253529,RMVar_hsa_circ_253530,RMVar_hsa_circ_253528,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_110832,RMVar_hsa_circ_87543,RMVar_hsa_circ_48040,RMVar_hsa_circ_54383,RMVar_hsa_circ_101109,RMVar_hsa_circ_253535,RMVar_hsa_circ_89504,RMVar_hsa_circ_253536,RMVar_hsa_circ_19130,RMVar_hsa_circ_27644,RMVar_hsa_circ_253537,RMVar_hsa_circ_272495,RMVar_hsa_circ_343640,RMVar_hsa_circ_366004,RMVar_hsa_circ_376185,RMVar_hsa_circ_277611,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_253542,RMVar_hsa_circ_53814,RMVar_hsa_circ_77140,RMVar_hsa_circ_253543,RMVar_hsa_circ_253544,RMVar_hsa_circ_253540,RMVar_hsa_circ_253541,RMVar_hsa_circ_253539,RMVar_hsa_circ_253545 115748 RMVar_ID_115748 Human_SNP_ID_874128422 m1A Human chr8 + 25507295 25507295 25507295 ATTCTGAACTGTTTAAAGATTTGTCTGATGCCATTGAGCAAACCTTTCAGAGGAGAAATAGTGAA ATTCTGAACTGTTTAAAGATTTGTCTGATGCCGTTGAGCAAACCTTTCAGAGGAGAAATAGTGAA A G CDCA2 Ensembl:ENSG00000184661 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79983029 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_8685211,Human_RBP_ID_9223304,Human_RBP_ID_24253776 Human_miRNA_ID_1409773 115749 RMVar_ID_115749 Human_SNP_ID_874134123 m1A Human chr8 + 127736393 127736393 127736393 CGCCTCTGGCCCAGCCCTCCCGCTGATCCCCCAGCCAGCGGTCCGCAACCCTTGCCGCATCCACG CGCCTCTGGCCCAGCCCTCCCGCTGATCCCCCGGCCAGCGGTCCGCAACCCTTGCCGCATCCACG A G MYC Ensembl:ENSG00000136997 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:127736297..127736425 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 10 haematopoietic and lymphoid tissue Human_RBP_ID_88454,Human_RBP_ID_795635,Human_RBP_ID_4995195,Human_RBP_ID_5453164,Human_RBP_ID_8923604,Human_RBP_ID_9313618,Human_RBP_ID_9338717,Human_RBP_ID_9405778,Human_RBP_ID_22115888,Human_RBP_ID_22534421 Human_miRNA_ID_2293910,Human_miRNA_ID_2331469,Human_miRNA_ID_2653193,Human_miRNA_ID_2684202,Human_miRNA_ID_2754390,Human_miRNA_ID_2964552 RMVar_hsa_circ_76158,RMVar_hsa_circ_111351,RMVar_hsa_circ_254315,RMVar_hsa_circ_254316 115750 RMVar_ID_115750 Human_SNP_ID_874144080 m1A Human chr8 - 100721579 100721579 100721579 CTGTGGCCCTGCGGGCAGCCGTGCCGAGATGAACCCCAGTGCCCCCAGCTACCCCATGGCCTCGC CTGTGGCCCTGCGGGCAGCCGTGCCGAGATGAGCCCCAGTGCCCCCAGCTACCCCATGGCCTCGC T C PABPC1 Ensembl:ENSG00000070756 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr8:100721370..100722046;chr8:100721426..100722075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_691985,Human_RBP_ID_795228,Human_RBP_ID_8676412,Human_RBP_ID_16300227,Human_RBP_ID_17433954,Human_RBP_ID_17543954,Human_RBP_ID_18889198,Human_RBP_ID_18961602,Human_RBP_ID_22534381,Human_RBP_ID_26141203,Human_RBP_ID_26552678 Human_Splice_Rec_997652,Human_Splice_Rec_997800,Human_Splice_Rec_997804,Human_Splice_Rec_997814 Human_miRNA_ID_2684190 RMVar_hsa_circ_98534,RMVar_hsa_circ_253524,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_253549 115751 RMVar_ID_115751 Human_SNP_ID_874152220 m1A Human chr8 + 100721674 100721674 100721674 GAGTGCCGGGGCTGGGGGCCGGAGCCGGGGGGAGGGGAGCGGGGAGCAAGCGCAGAGGGACAAAA GAGTGCCGGGGCTGGGGGCCGGAGCCGGGGGGGGGGGAGCGGGGAGCAAGCGCAGAGGGACAAAA A G lnc-SPAG1-7 RNACentral:URS00008C0CD5 lincRNA exon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Starvation treatment;HEK293T,untreat control chr8:100721575..100721878;chr8:100721576..100721867 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115752 RMVar_ID_115752 Human_SNP_ID_874182847 m1A Human chr8 + 22247911 22247911 22247911 AAGAAGGAGAAGCGTGAAAGGGACAGAGACCGACAACGAGAGGGGCATGGACGAGGGCGAGGCCG AAGAAGGAGAAGCGTGAAAGGGACAGAGACCGGCAACGAGAGGGGCATGGACGAGGGCGAGGCCG A G POLR3D Ensembl:ENSG00000168495 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22247829..22247966 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_845280,Human_RBP_ID_960433,Human_RBP_ID_4978558,Human_RBP_ID_9405250,Human_RBP_ID_24549445,Human_RBP_ID_26358870,Human_RBP_ID_27831159 Human_Splice_Rec_956552,Human_Splice_Rec_956553,Human_Splice_Rec_956568,Human_Splice_Rec_956569,Human_Splice_Rec_956576,Human_Splice_Rec_956577,Human_Splice_Rec_956590,Human_Splice_Rec_956591,Human_Splice_Rec_956598,Human_Splice_Rec_956599 RMVar_hsa_circ_18630,RMVar_hsa_circ_103036,RMVar_hsa_circ_103979,RMVar_hsa_circ_250707,RMVar_hsa_circ_48852,RMVar_hsa_circ_126357,RMVar_hsa_circ_49915,RMVar_hsa_circ_250708,RMVar_hsa_circ_330804,RMVar_hsa_circ_250709,RMVar_hsa_circ_83538,RMVar_hsa_circ_250710,RMVar_hsa_circ_250711 115753 RMVar_ID_115753 Human_SNP_ID_874202588 m1A Human chr8 - 37696199 37696199 37696199 GGGACTGACCTCAATGGGGCTGACGGGAGTGGAGGACAGCGGCTGCAGGTACTCCGGGTGCAGGA GGGACTGACCTCAATGGGGCTGACGGGAGTGGTGGACAGCGGCTGCAGGTACTCCGGGTGCAGGA T A lnc-BRF2-3 RNACentral:URS0000D5C499 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:37695800..37697722 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung 115754 RMVar_ID_115754 Human_SNP_ID_874208018 m1A Human chr8 - 61684190 61684190 61684190 CTTCTTATGATATCTTACATTTATTTCTAAACAGAGACAAAGCATGGAGGACACAAGAATGGGAG CTTCTTATGATATCTTACATTTATTTCTAAACCGAGACAAAGCATGGAGGACACAAGAATGGGAG T G ASPH Ensembl:ENSG00000198363 Protein coding intron GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr8:61684159..61684252;chr8:61684176..61684200 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon tubular,colon adenocarcinoma,sigmoid high_grade_dysplasia,large_intestine tubular,large_intestine adenocarcinoma 28 colon,large intestine RMVar_hsa_circ_93208,RMVar_hsa_circ_252329 115755 RMVar_ID_115755 Human_SNP_ID_874216717 m1A Human chr8 + 1839751 1839751 1839751 GGACTGTCCGGTGTGGAAGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGG GGACTGTCCGGTGTGGAAGCTGTCTGGTGTGGGAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGG A G AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:1839744..1839930 26863196 MeRIP-seq:(Medium) rs1474699760 Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_346810 115756 RMVar_ID_115756 Human_SNP_ID_874229728 m1A Human chr8 - 30791308 30791308 30791308 TAATGAATTTGTTTTTATCCTGCAGGGATACAATTGGTGTCATGATCGGAATGTGGTTACCATTT TAATGAATTTGTTTTTATCCTGCAGGGATACAGTTGGTGTCATGATCGGAATGTGGTTACCATTT T C PPP2CB Ensembl:ENSG00000104695 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:30791257..30791357 32194978 MeRIP-seq:(Medium) rs1296593420 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_698577,Human_RBP_ID_8919078 Human_Splice_Rec_963864,Human_Splice_Rec_963874 RMVar_hsa_circ_30390,RMVar_hsa_circ_251131,RMVar_hsa_circ_81964,RMVar_hsa_circ_372941,RMVar_hsa_circ_251132,RMVar_hsa_circ_377620,RMVar_hsa_circ_302638,RMVar_hsa_circ_251133,RMVar_hsa_circ_251134 115757 RMVar_ID_115757 Human_SNP_ID_874269198 m1A Human chr8 + 125245168 125245168 125245168 AGCCCGGCGTGGTGGTGGACACCTGTAAGCCCAGCTACTGGGGAGGATGAGGCAGGAGAATCACT AGCCCGGCGTGGTGGTGGACACCTGTAAGCCCGGCTACTGGGGAGGATGAGGCAGGAGAATCACT A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:125245166..125245300 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_85279,RMVar_hsa_circ_254296,RMVar_hsa_circ_254300,RMVar_hsa_circ_122444,RMVar_hsa_circ_106087,RMVar_hsa_circ_81897,RMVar_hsa_circ_254299,RMVar_hsa_circ_254304,RMVar_hsa_circ_103178,RMVar_hsa_circ_254308 115758 RMVar_ID_115758 Human_SNP_ID_874272801 m1A Human chr8 - 60558859 60558859 60558859 TTGTCTGTAAACTGTAGCAATAAGCATGATTTACCAACACCTGAAAGTTAAAAAAAAATAAATAA TTGTCTGTAAACTGTAGCAATAAGCATGATTTGCCAACACCTGAAAGTTAAAAAAAAATAAATAA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:60558851..60558875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 3 haematopoietic and lymphoid tissue 115759 RMVar_ID_115759 Human_SNP_ID_874358982 m1A Human chr8 - 23255386 23255386 23255386 GCTCGAGGACTGTGACCCTCTTCTCCTTCTGCAGCTGCAGCAACACCAAGTAGAAGGTCCTCTCA GCTCGAGGACTGTGACCCTCTTCTCCTTCTGCTGCTGCAGCAACACCAAGTAGAAGGTCCTCTCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:23255265..23255416 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 115760 RMVar_ID_115760 Human_SNP_ID_874366708 m1A Human chr8 + 97661171 97661171 97661171 AGCAGCCACCAGAGATTGACAAGAAAAATGAAAAGGTAAGTTTGGGAGCATATGAAATTGTATGC AGCAGCCACCAGAGATTGACAAGAAAAATGAAGAGGTAAGTTTGGGAGCATATGAAATTGTATGC A G MTDH Ensembl:ENSG00000147649 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:97661154..97661228 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_2058398,Human_RBP_ID_9351431 Human_Splice_Rec_995440,Human_Splice_Rec_995441,Human_Splice_Rec_995462,Human_Splice_Rec_995463,Human_Splice_Rec_995482,Human_Splice_Rec_995483 RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_275797,RMVar_hsa_circ_292754,RMVar_hsa_circ_338777,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253291,RMVar_hsa_circ_253292,RMVar_hsa_circ_253289 115761 RMVar_ID_115761 Human_SNP_ID_874398054 m1A Human chr8 - 23317094 23317094 23317094 TGGTTCTTCCAGGAGACCTGGTATTGGCACGGAGATGTCAACAGCAACAAAGTGGTCATGAGTGG TGGTTCTTCCAGGAGACCTGGTATTGGCACGGCGATGTCAACAGCAACAAAGTGGTCATGAGTGG T G LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23316906..23317158 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_Splice_Rec_958486,Human_Splice_Rec_958498 Human_miRNA_ID_1533499,Human_miRNA_ID_1536266,Human_miRNA_ID_2464820,Human_miRNA_ID_2721823 RMVar_hsa_circ_11094,RMVar_hsa_circ_45914,RMVar_hsa_circ_28168,RMVar_hsa_circ_53278,RMVar_hsa_circ_250782,RMVar_hsa_circ_109885,RMVar_hsa_circ_331761,RMVar_hsa_circ_343155,RMVar_hsa_circ_348092,RMVar_hsa_circ_118425,RMVar_hsa_circ_48673,RMVar_hsa_circ_116267,RMVar_hsa_circ_250783,RMVar_hsa_circ_250784 115762 RMVar_ID_115762 Human_SNP_ID_874442308 m1A Human chr8 + 70586998 70586998 70586998 TAGCACCAGAAGAACAAGTCCTAGATGATTCAAGCTGTTAAAAGAGCAAATTAAAAATGGGAATA TAGCACCAGAAGAACAAGTCCTAGATGATTCATGCTGTTAAAAGAGCAAATTAAAAATGGGAATA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:70586964..70587170 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 115763 RMVar_ID_115763 Human_SNP_ID_874455843 m1A Human chr8 - 51817881 51817881 51817881 CCTAGAACCGTGGCATGTTTTGCCTGAAACATACAGTGAGTTAGAGACAGGGCCTAAGATAGCTT CCTAGAACCGTGGCATGTTTTGCCTGAAACATGCAGTGAGTTAGAGACAGGGCCTAAGATAGCTT T C PCMTD1 Ensembl:ENSG00000168300 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6768 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_24260791 GWAS_ID_10642,GWAS_ID_10643,GWAS_ID_10644 RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 115764 RMVar_ID_115764 Human_SNP_ID_874460664 m1A Human chr8 - 38917966 38917966 38917966 GCCGCTGTTCTCATGCTCCTCGATGTCCAGAAACCCACAGATTCGGTTCTGCCGATCCACATAAG GCCGCTGTTCTCATGCTCCTCGATGTCCAGAAGCCCACAGATTCGGTTCTGCCGATCCACATAAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:38917871..38917992 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 115765 RMVar_ID_115765 Human_SNP_ID_874468874 m1A Human chr8 + 80487334 80487334 80487334 GCTGGACGCGCTGGAGGGGAAGGAGTTGATGCAGGACGGCGCGTCCCTGAGCGACAGCACCGAGG GCTGGACGCGCTGGAGGGGAAGGAGTTGATGCTGGACGGCGCGTCCCTGAGCGACAGCACCGAGG A T ZBTB10 Ensembl:ENSG00000205189 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:80486947..80487629 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_22115052,Human_RBP_ID_23120777,Human_RBP_ID_27831965 RMVar_hsa_circ_252818 115766 RMVar_ID_115766 Human_SNP_ID_874482869 m1A Human chr8 - 22618941 22618941 22618941 GCCGGCCGCTGTCCTGCTGCTCCGCGCGCTGCAGCAGGCTCCCCACGTTAATCAGGCTGCCATTG GCCGGCCGCTGTCCTGCTGCTCCGCGCGCTGCGGCAGGCTCCCCACGTTAATCAGGCTGCCATTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22618890..22619015 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_27537489 115767 RMVar_ID_115767 Human_SNP_ID_874486638 m1A Human chr8 - 38917960 38917959 38917961 GTTCTCATGCTCCTCGATGTCCAGAAACCCACAGATTCGGTTCTGCCGATCCACATAAGGCATTC GTTCTCATGCTCCTCGATGTCCAGAAACCCA__GATTCGGTTCTGCCGATCCACATAAGGCATTC CTG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:38917847..38917980 26863196 MeRIP-seq:(Medium) rs940962664 Functional Loss DEL TCGA 32..33 33 KIRC 1 - 115768 RMVar_ID_115768 Human_SNP_ID_874489850 m1A Human chr8 - 127738451 127738451 127738451 TAGGAGGGCGAGCAGAGCCCGGAGCGGCGGCTAGGGGACAGGGGCGGGGTGGGCAGCAGCTCGAA TAGGAGGGCGAGCAGAGCCCGGAGCGGCGGCTGGGGGACAGGGGCGGGGTGGGCAGCAGCTCGAA T C CASC11 Ensembl:ENSG00000249375 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:127738223..127738956 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 115769 RMVar_ID_115769 Human_SNP_ID_874494079 m1A Human chr8 - 12755305 12755305 12755305 GGAAGTGGGCGGCGGCAGCGGCCATCGGCTGGAGCGCGCGGCCGCGGAGTCGGAGCGCTGGGAGC GGAAGTGGGCGGCGGCAGCGGCCATCGGCTGGGGCGCGCGGCCGCGGAGTCGGAGCGCTGGGAGC T C LONRF1 Ensembl:ENSG00000154359 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12755255..12755454 26863196 MeRIP-seq:(Medium) rs1004380421 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_796373,Human_RBP_ID_4994906,Human_RBP_ID_18466990 115770 RMVar_ID_115770 Human_SNP_ID_874542299 m1A Human chr8 - 61714390 61714390 61714390 CGCGCACTGAAGGAGGTCCGCCAGCCCTCACCAGCCCCCGCGGACCGTGCAATGGCCCAGCGTAA CGCGCACTGAAGGAGGTCCGCCAGCCCTCACCTGCCCCCGCGGACCGTGCAATGGCCCAGCGTAA T A ASPH Ensembl:ENSG00000198363 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:61714251..61714550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_90019,Human_RBP_ID_702419,Human_RBP_ID_796553,Human_RBP_ID_4989602,Human_RBP_ID_9405533,Human_RBP_ID_26359149,Human_RBP_ID_27831924 115771 RMVar_ID_115771 Human_SNP_ID_874548288 m1A Human chr8 + 141194117 141194114 141194117 ACGTGATTGACGCCGAGAGGAAGACCGTGGAGAAGGAGCTGGTGGCGCACATGGACACCGTGAGG ACGTGATTGACGCCGAGAGGAAGACCGTGG___AGGAGCTGGTGGCGCACATGGACACCGTGAGG GAGA G DENND3 Ensembl:ENSG00000105339 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:141194066..141194237 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 COAD 1 - Human_Splice_Rec_1016966,Human_Splice_Rec_1017010,Human_Splice_Rec_1017072,Human_Splice_Rec_1017112,Human_Splice_Rec_1017160,Human_Splice_Rec_1017166 115772 RMVar_ID_115772 Human_SNP_ID_874589496 m1A Human chr8 - 23290381 23290381 23290381 CCACCTCCTCTTCGTCCTCTTCCTCCTCTGCCACCAGCCTCTTCTCCAACAGACTCTCCTTCCCC CCACCTCCTCTTCGTCCTCTTCCTCCTCTGCCCCCAGCCTCTTCTCCAACAGACTCTCCTTCCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23290262..23290475 26863196 MeRIP-seq:(Medium) rs202214700 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 3 head and neck 115773 RMVar_ID_115773 Human_SNP_ID_874594918 m1A Human chr8 - 731145 731145 731145 CGCGGCAGGGTCCCGCATGGCGGCGCACAGGAAGCACGGTAGGTGGGTGCGGTGCGGAGGCCTGC CGCGGCAGGGTCCCGCATGGCGGCGCACAGGAGGCACGGTAGGTGGGTGCGGTGCGGAGGCCTGC T C ERICH1 Ensembl:ENSG00000104714 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:692583..731173 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_4995329,Human_RBP_ID_23088037 Human_Splice_Rec_944361,Human_Splice_Rec_944383 RMVar_hsa_circ_103571,RMVar_hsa_circ_249966 115774 RMVar_ID_115774 Human_SNP_ID_874595098 m1A Human chr8 - 19817602 19817602 19817602 GGGCCGTGATCAGCCACGCCTTGGCTGCCCACAGGTCTTGCGGCACCAACTCCCGGGCTCGCTGC GGGCCGTGATCAGCCACGCCTTGGCTGCCCACGGGTCTTGCGGCACCAACTCCCGGGCTCGCTGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr8:19817484..19817633;chr8:19817551..19818214 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 115775 RMVar_ID_115775 Human_SNP_ID_874633266 m1A Human chr8 + 144106916 144106916 144106916 CTGGGGGAGGAGGAGGTGGAGGAAGAAAGCAGAAGCGGGGGCAGTGGGGCCGAGGAGACCAGCAC CTGGGGGAGGAGGAGGTGGAGGAAGAAAGCAGCAGCGGGGGCAGTGGGGCCGAGGAGACCAGCAC A C MAF1 Ensembl:ENSG00000179632 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144106848..144106975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_18196822 Human_Splice_Rec_1022624,Human_Splice_Rec_1022625,Human_Splice_Rec_1022636,Human_Splice_Rec_1022637,Human_Splice_Rec_1022650,Human_Splice_Rec_1022651,Human_Splice_Rec_1022666,Human_Splice_Rec_1022668 RMVar_hsa_circ_115766,RMVar_hsa_circ_255038,RMVar_hsa_circ_93211,RMVar_hsa_circ_88454,RMVar_hsa_circ_97054,RMVar_hsa_circ_255039,RMVar_hsa_circ_255040,RMVar_hsa_circ_105353,RMVar_hsa_circ_255042,RMVar_hsa_circ_255043 115776 RMVar_ID_115776 Human_SNP_ID_874647884 m1A Human chr8 + 23404089 23404089 23404089 GCTCTGGTCTCCGATGGCTGGAGAAAGCAAGCACCAAGCGTAGGTAGCCGCGCGCTGGAGTCGCG GCTCTGGTCTCCGATGGCTGGAGAAAGCAAGCGCCAAGCGTAGGTAGCCGCGCGCTGGAGTCGCG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:23403920..23404100;chr8:23403900..23404150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115777 RMVar_ID_115777 Human_SNP_ID_874706565 m1A Human chr8 - 11802815 11802815 11802815 TTTCACGAACTCCATCCTGGCGCAGGCGGCGGACTCCCGGGCGCGACTCTCACCTCTGCGGTCCC TTTCACGAACTCCATCCTGGCGCAGGCGGCGGCCTCCCGGGCGCGACTCTCACCTCTGCGGTCCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:11802726..11802974;chr8:11802726..11802979;chr8:11802751..11802950;chr8:11802726..11802950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 7 oesophagus 115778 RMVar_ID_115778 Human_SNP_ID_874727364 m1A Human chr8 + 8891188 8891188 8891188 AGTGGCGCGGGTCCCTGCAGCTAACAGGCAACACGGGGGAGAGGATCTGCAGCCGGTGGTTGAGC AGTGGCGCGGGTCCCTGCAGCTAACAGGCAACCCGGGGGAGAGGATCTGCAGCCGGTGGTTGAGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:8891138..8891210 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115779 RMVar_ID_115779 Human_SNP_ID_874727367 m1A Human chr8 + 8891188 8891188 8891188 AGTGGCGCGGGTCCCTGCAGCTAACAGGCAACACGGGGGAGAGGATCTGCAGCCGGTGGTTGAGC AGTGGCGCGGGTCCCTGCAGCTAACAGGCAACGCGGGGGAGAGGATCTGCAGCCGGTGGTTGAGC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:8891138..8891210 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115780 RMVar_ID_115780 Human_SNP_ID_874738827 m1A Human chr8 - 140545129 140545129 140545129 GGATGTGGGCGGAGAGTGAGTCACAGGCATGCAGGGAAATGGATGCGGGGAGAGGGCAGCAGAGG GGATGTGGGCGGAGAGTGAGTCACAGGCATGCGGGGAAATGGATGCGGGGAGAGGGCAGCAGAGG T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:140545126..140545263 26863196 MeRIP-seq:(Medium) rs2944770 Functional Loss SNV ICGC 33..33 33 LUSC 1 - GWAS_ID_7881 RMVar_hsa_circ_369948,RMVar_hsa_circ_254671,RMVar_hsa_circ_10339,RMVar_hsa_circ_343080,RMVar_hsa_circ_254673,RMVar_hsa_circ_269128,RMVar_hsa_circ_358666,RMVar_hsa_circ_37102,RMVar_hsa_circ_298373,RMVar_hsa_circ_16504,RMVar_hsa_circ_254675,RMVar_hsa_circ_4690,RMVar_hsa_circ_301532,RMVar_hsa_circ_254676 115781 RMVar_ID_115781 Human_SNP_ID_874741169 m1A Human chr8 - 22591652 22591652 22591652 CCCCCTCCACACTCACGCGATGCTGGTACTGCACTTCTCACAAGTGTGGAGCTTGGGAGGGGTGG CCCCCTCCACACTCACGCGATGCTGGTACTGCGCTTCTCACAAGTGTGGAGCTTGGGAGGGGTGG T C lnc-BIN3-2 RNACentral:URS00008BCC24 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22589276..22593868 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 14 uterus 115782 RMVar_ID_115782 Human_SNP_ID_874758899 m1A Human chr8 + 127226000 127226000 127226000 ATGGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGAGAAGATCACTTTAGCACAGAAATTCTA ATGGCCTGTAATCCCAGCACTTTGGGAGGCCATGGTGAGAAGATCACTTTAGCACAGAAATTCTA A T PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:127225976..127226000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 115783 RMVar_ID_115783 Human_SNP_ID_874813783 m1A Human chr8 + 80171477 80171477 80171477 TCTCCAGCCCGCCGCCTCGTGTCCTCTGCAGCACCCCCGCCTGCAGCCCGTCCCGGCTCGGATCG TCTCCAGCCCGCCGCCTCGTGTCCTCTGCAGCCCCCCCGCCTGCAGCCCGTCCCGGCTCGGATCG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr8:80171308..80171583;chr8:80171351..80171559 26863196 MeRIP-seq:(Medium) rs781464657 Functional Loss SNV ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 115784 RMVar_ID_115784 Human_SNP_ID_874838513 m1A Human chr8 + 123369101 123369101 123369101 TTTACAGTAAGGACTTCTTGGTCCTGCGGAAGATAATCGGTATCTTGGTCTTGCAGGAGAAGCTG TTTACAGTAAGGACTTCTTGGTCCTGCGGAAGTTAATCGGTATCTTGGTCTTGCAGGAGAAGCTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:123369051..123369100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 2 lung 115785 RMVar_ID_115785 Human_SNP_ID_874845024 m1A Human chr8 + 143805332 143805332 143805332 GCGGCGTGATGGTGACCGCGTTCTCAGGCTCCACCATGCGCTCCCGCCACACTCGCATCTGCACG GCGGCGTGATGGTGACCGCGTTCTCAGGCTCCCCCATGCGCTCCCGCCACACTCGCATCTGCACG A C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:143805230..143805380 26863410 MeRIP-seq:(Medium) rs1554636280 Functional Loss SNV ICGC 33..33 33 THCA 1 - 115786 RMVar_ID_115786 Human_SNP_ID_874847618 m1A Human chr8 - 28099906 28099906 28099906 TTTAACTTGGGCATCAAGACCTTGCGATACTGAGGAGGGACGGCAGCAATGATATCCACCAGGCG TTTAACTTGGGCATCAAGACCTTGCGATACTGTGGAGGGACGGCAGCAATGATATCCACCAGGCG T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:28099856..28107931 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 115787 RMVar_ID_115787 Human_SNP_ID_874850254 m1A Human chr8 - 37698444 37698444 37698444 GGCGGCGGGCGGGGGGAGGTGCAGATGGCAGGAGGCGGCGGCGGCGGCGGCGGCGGCGGCGCTGC GGCGGCGGGCGGGGGGAGGTGCAGATGGCAGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGCTGC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:37698083..37698713 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115788 RMVar_ID_115788 Human_SNP_ID_874855791 m1A Human chr8 + 143647673 143647673 143647673 GAGGGCAGGGTGAGCAGCAGGAGTCCAGGCCCAGTGGCCCTTGTGGGGCCAGAGTAGGGGATGGG GAGGGCAGGGTGAGCAGCAGGAGTCCAGGCCCGGTGGCCCTTGTGGGGCCAGAGTAGGGGATGGG A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143647667..143648203 26863196 MeRIP-seq:(Medium) rs7827272 Functional Loss SNV COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,frontal_lobe astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_II,frontal_lobe oligodendroglioma_Grade_III 6 brain 115789 RMVar_ID_115789 Human_SNP_ID_874871342 m1A Human chr8 + 22201192 22201192 22201192 AGCTCAAATTCCGAGTGCAGAAAAGAAACCGGACCCCCCAGTGAGGCCTGCCAGGCCTCCCGGAC AGCTCAAATTCCGAGTGCAGAAAAGAAACCGGGCCCCCCAGTGAGGCCTGCCAGGCCTCCCGGAC A G BMP1 Ensembl:ENSG00000168487 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22201118..22201403 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_Splice_Rec_956196,Human_Splice_Rec_956232,Human_Splice_Rec_956262,Human_Splice_Rec_956330,Human_Splice_Rec_956420,Human_Splice_Rec_956450,Human_Splice_Rec_956482,Human_Splice_Rec_956510 RMVar_hsa_circ_2186 115790 RMVar_ID_115790 Human_SNP_ID_874883324 m1A Human chr8 + 1839752 1839752 1839752 GACTGTCCGGTGTGGAAGCTGTCTGGTGTGGAAGCTGTCTGGTGTGGGGACTGTCTGGTGTGGGT GACTGTCCGGTGTGGAAGCTGTCTGGTGTGGACGCTGTCTGGTGTGGGGACTGTCTGGTGTGGGT A C AC019257.8,ARHGEF10 Ensembl:ENSG00000283239,Ensembl:ENSG00000104728 Protein coding,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:1839748..1839863 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_346810 115791 RMVar_ID_115791 Human_SNP_ID_874892627 m1A Human chr8 + 91040704 91040704 91040704 TGGGGCGGTGGGAGTGACATTTCCGGAGTGGGATGCTGACAGCAGAGGCGAGCGTTCGTCCACCC TGGGGCGGTGGGAGTGACATTTCCGGAGTGGGCTGCTGACAGCAGAGGCGAGCGTTCGTCCACCC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:91040597..91040916 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 115792 RMVar_ID_115792 Human_SNP_ID_874951722 m1A Human chr8 + 144309504 144309503 144309505 GTCCACATCGAGCAGGGCGGCCTGGTCAAGCCAGAGAGAGACGACACGGAGTTCCAGCACCCATG GTCCACATCGAGCAGGGCGGCCTGGTCAAGCC__AGAGAGACGACACGGAGTTCCAGCACCCATG CAG C HSF1 Ensembl:ENSG00000185122 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144309427..144309529 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 UCEC 1 - Human_RBP_ID_255120,Human_RBP_ID_959610,Human_RBP_ID_4996459,Human_RBP_ID_26833088 Human_Splice_Rec_1023400,Human_Splice_Rec_1023401,Human_Splice_Rec_1023424,Human_Splice_Rec_1023425,Human_Splice_Rec_1023452,Human_Splice_Rec_1023454,Human_Splice_Rec_1023455,Human_Splice_Rec_1023461,Human_Splice_Rec_1023479,Human_Splice_Rec_1023485,Human_Splice_Rec_1023487 Human_miRNA_ID_2464843 RMVar_hsa_circ_37512,RMVar_hsa_circ_53459,RMVar_hsa_circ_375632,RMVar_hsa_circ_51615,RMVar_hsa_circ_324507,RMVar_hsa_circ_5403,RMVar_hsa_circ_29146,RMVar_hsa_circ_255089 115793 RMVar_ID_115793 Human_SNP_ID_874978947 m1A Human chr8 - 8376829 8376829 8376829 GACTTCGGCTGGGCAGGGGCTGAGCTCCAGGGAAAGCCATGCTCACAGTGCCAGCGAGAGCAAGC GACTTCGGCTGGGCAGGGGCTGAGCTCCAGGGCAAGCCATGCTCACAGTGCCAGCGAGAGCAAGC T G PRAG1 Ensembl:ENSG00000275342 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:8376781..8376889 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_5534044,Human_RBP_ID_19022523 RMVar_hsa_circ_346666,RMVar_hsa_circ_280582 115794 RMVar_ID_115794 Human_SNP_ID_874986356 m1A Human chr8 + 143984605 143984603 143984606 GTGGCAAGAGAGCGACGTCTCCCAGGCCCGCAAGAAGGTCCTCATGGTAGAGCTGCAGGAAGCGC GTGGCAAGAGAGCGACGTCTCCCAGGCCCGC___AAGGTCCTCATGGTAGAGCTGCAGGAAGCGC CAAG C RF00017-4575,RF00017-1304 RNACentral:URS0000918622,RNACentral:URS0000990DE9 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143984581..143984969 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 STAD 1 - 115795 RMVar_ID_115795 Human_SNP_ID_874996810 m1A Human chr8 + 144395322 144395322 144395322 CTCCTCGCCAGTCATGCGTGGGATGCGGGCACACGGCGTGTTGGTGCTGGTGGCCACAGCATACA CTCCTCGCCAGTCATGCGTGGGATGCGGGCACGCGGCGTGTTGGTGCTGGTGGCCACAGCATACA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144395276..144395375 26863196 MeRIP-seq:(Medium) rs1222441007 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 115796 RMVar_ID_115796 Human_SNP_ID_875015769 m1A Human chr8 - 143808685 143808684 143808685 TCAGGAGGAGGAGGAAGAGGAGGAGGAGGAAAACAGGGCTGAAGAGGAAGAGGCCAGCACTGAGG TCAGGAGGAGGAGGAAGAGGAGGAGGAGGAAA_CAGGGCTGAAGAGGAAGAGGCCAGCACTGAGG GT G SCRIB Ensembl:ENSG00000180900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143806937..143809044;chr8:143805101..143810504;chr8:143808588..143808959 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BRCA 1 - Human_RBP_ID_89983,Human_RBP_ID_3973413,Human_RBP_ID_5123673,Human_RBP_ID_5534352,Human_RBP_ID_8917152,Human_RBP_ID_22689412,Human_RBP_ID_23084052,Human_RBP_ID_26359433 Human_Splice_Rec_1020531,Human_Splice_Rec_1020603,Human_Splice_Rec_1020713,Human_Splice_Rec_1020785,Human_Splice_Rec_1020839 115797 RMVar_ID_115797 Human_SNP_ID_875027902 m1A Human chr8 - 98102845 98102845 98102845 GCTATCCAAGGACCACTGACAACGGCATCACTATAAGTGGGCCCAGTGCTGTGTAGTCTGGAATT GCTATCCAAGGACCACTGACAACGGCATCACTGTAAGTGGGCCCAGTGCTGTGTAGTCTGGAATT T C RIDA Ensembl:ENSG00000132541 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs370041963 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_706862,Human_RBP_ID_9229780 Human_Splice_Rec_995908,Human_Splice_Rec_995918,Human_Splice_Rec_995928,Human_Splice_Rec_995936,Human_Splice_Rec_995942 115798 RMVar_ID_115798 Human_SNP_ID_875046472 m1A Human chr8 + 27491199 27491199 27491199 GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGACCCGCCGCCATGACGCTGCGCGCGGCCGTCTT GGTTAGCTGCGTGTCCGGGTGCTAGGCTGCAGGCCCGCCGCCATGACGCTGCGCGCGGCCGTCTT A G EPHX2 Ensembl:ENSG00000120915 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27491194..27491259 26863196 MeRIP-seq:(Medium) rs905914545 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4995389,Human_RBP_ID_9313351 Human_Splice_Rec_960968 115799 RMVar_ID_115799 Human_SNP_ID_875057245 m1A Human chr8 + 143430625 143430625 143430625 CTAGGGGCACCGCTGGCCAGGTGTCTCGGGCGACCCCGGGCCCGCGTCGCCGCCTCCTCCCCGCG CTAGGGGCACCGCTGGCCAGGTGTCTCGGGCGTCCCCGGGCCCGCGTCGCCGCCTCCTCCCCGCG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143430574..143430711 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115800 RMVar_ID_115800 Human_SNP_ID_875079345 m1A Human chr8 - 144514463 144514463 144514463 GCCTGCATACACTCGGGCATGACCAGGAAGCAACGGGAATCTGTCCTGCAGAAGGTGGGGGCCTC GCCTGCATACACTCGGGCATGACCAGGAAGCAGCGGGAATCTGTCCTGCAGAAGGTGGGGGCCTC T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:144514022..144514600;chr8:144514071..144514650 26863196 MeRIP-seq:(Medium) rs1332576218 Functional Loss SNV TCGA 33..33 33 LGG 1 - Human_RBP_ID_1694244,Human_RBP_ID_3974389,Human_RBP_ID_18452349 Human_Splice_Rec_1024968,Human_Splice_Rec_1024969,Human_Splice_Rec_1025006,Human_Splice_Rec_1025007,Human_Splice_Rec_1025051,Human_Splice_Rec_1025074,Human_Splice_Rec_1025075 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 115801 RMVar_ID_115801 Human_SNP_ID_875124891 m1A Human chr8 - 143837140 143837140 143837140 ATGGAATCTACCCACTGATGAACTTTGCAGCCACTCGACCCCTGGGGCTGCCCCGTGTGCTGGCC ATGGAATCTACCCACTGATGAACTTTGCAGCCGCTCGACCCCTGGGGCTGCCCCGTGTGCTGGCC T C NRBP2 Ensembl:ENSG00000185189 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143837132..143837238 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 2 lung Human_RBP_ID_9406606,Human_RBP_ID_19023202 Human_Splice_Rec_1021156,Human_Splice_Rec_1021188,Human_Splice_Rec_1021214,Human_Splice_Rec_1021226,Human_Splice_Rec_1021262,Human_Splice_Rec_1021292,Human_Splice_Rec_1021304 115802 RMVar_ID_115802 Human_SNP_ID_875138023 m1A Human chr8 - 81280636 81280636 81280636 CCTTCATGTATTCATCAAAGCCTTTGCTGTCCACCAGGCGCCATCTTCCTTCCAGCTGCTGAACT CCTTCATGTATTCATCAAAGCCTTTGCTGTCCGCCAGGCGCCATCTTCCTTCCAGCTGCTGAACT T C AC009902.2 Ensembl:ENSG00000254027 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr8:81280535..81280640 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 2 liver Human_Splice_Rec_988241 115803 RMVar_ID_115803 Human_SNP_ID_875246658 m1A Human chr8 + 55773319 55773319 55773319 GCTCTTCGGGGGATCAGTGGCCAAGGGGGCGGACAGATTTGCACGGCGGATTCCTCCGAAGCAAC GCTCTTCGGGGGATCAGTGGCCAAGGGGGCGGGCAGATTTGCACGGCGGATTCCTCCGAAGCAAC A G RF00017-4497,RF00017-4675,RF00017-4706 RNACentral:URS0000961FEC,RNACentral:URS00009156E9,RNACentral:URS000095B12E SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:55773228..55773353;chr8:55773243..55773329 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - RMVar_hsa_circ_117781,RMVar_hsa_circ_252160 115804 RMVar_ID_115804 Human_SNP_ID_875305016 m1A Human chr8 - 11847815 11847815 11847815 TCCGCTTTCTCCCGCGTCCCATCAGGGTGCAGACCGTACTCCATCCCTCCCTGTGAGCACCACGT TCCGCTTTCTCCCGCGTCCCATCAGGGTGCAGGCCGTACTCCATCCCTCCCTGTGAGCACCACGT T C CTSB Ensembl:ENSG00000164733 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:11847776..11847825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach Human_RBP_ID_795857,Human_RBP_ID_17433780,Human_RBP_ID_18472466,Human_RBP_ID_22465081,Human_RBP_ID_22688053,Human_RBP_ID_22775604,Human_RBP_ID_22836111 Human_Splice_Rec_949462,Human_Splice_Rec_949470,Human_Splice_Rec_949488,Human_Splice_Rec_949510,Human_Splice_Rec_949532,Human_Splice_Rec_949550,Human_Splice_Rec_949570,Human_Splice_Rec_949590,Human_Splice_Rec_949610,Human_Splice_Rec_949626,Human_Splice_Rec_949632,Human_Splice_Rec_949640 Human_miRNA_ID_2029093,Human_miRNA_ID_2689605,Human_miRNA_ID_2692834 RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_8724,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247 115805 RMVar_ID_115805 Human_SNP_ID_875314607 m1A Human chr8 - 22108237 22108237 22108237 AGGGGAGACCATCGTGGAGGCGCTGCAGCGGGAGGTGAAGGAGGAGGCGGGGCTGCACTGTGAGC AGGGGAGACCATCGTGGAGGCGCTGCAGCGGGCGGTGAAGGAGGAGGCGGGGCTGCACTGTGAGC T G NUDT18 Ensembl:ENSG00000275074 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22108187..22108345 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary endometrioid_carcinoma 2 ovary Human_RBP_ID_19021809 RMVar_hsa_circ_8858,RMVar_hsa_circ_92227,RMVar_hsa_circ_250692 115806 RMVar_ID_115806 Human_SNP_ID_875326214 m1A Human chr8 + 23224672 23224672 23224672 ACATGCCCCGCCACAAGTGACCCGGGCCAGGCACCCCCGCCGCGTCCCCCTCTCTCTCTGCCCCC ACATGCCCCGCCACAAGTGACCCGGGCCAGGCCCCCCCGCCGCGTCCCCCTCTCTCTCTGCCCCC A C AC100861.1 Ensembl:ENSG00000246582 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:23224662..23224742 26863196 MeRIP-seq:(Medium) rs1039694135 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115807 RMVar_ID_115807 Human_SNP_ID_875340618 m1A Human chr8 + 33496741 33496741 33496741 GAGGAAAAAGATGATGATGATGATGATGAGGAAGTAAGTCTTGTTTTTGTTTTGCCAAACCTACT GAGGAAAAAGATGATGATGATGATGATGAGGACGTAAGTCTTGTTTTTGTTTTGCCAAACCTACT A C MAK16 Ensembl:ENSG00000198042 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr8:33496716..33496784;chr8:33496691..33496784 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_3156428 Human_Splice_Rec_964921,Human_Splice_Rec_964937 Human_miRNA_ID_2998447 RMVar_hsa_circ_86342,RMVar_hsa_circ_366965,RMVar_hsa_circ_251234,RMVar_hsa_circ_103068,RMVar_hsa_circ_251235,RMVar_hsa_circ_355416,RMVar_hsa_circ_354379,RMVar_hsa_circ_332476 115808 RMVar_ID_115808 Human_SNP_ID_875361883 m1A Human chr8 - 26577307 26577307 26577307 CTGGAACGGCGGCGGGCGGGAACCCGGCGGGGAGGGCCCGGCCACGCCCGGCCCCGGAGAGGGCG CTGGAACGGCGGCGGGCGGGAACCCGGCGGGGGGGGCCCGGCCACGCCCGGCCCCGGAGAGGGCG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26577275..26577390 26863196 MeRIP-seq:(Medium) rs937327616 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115809 RMVar_ID_115809 Human_SNP_ID_875393939 m1A Human chr8 - 116646584 116646564 116646585 CTTTGAATTTTAGTATCAGCAGCGTCGCCAGCAGGAGAATATGCAGCGCCAGAGCCGAGGAGAAC CTTTGAATTTTAGTATCAGCAGCGTCGCCAG_____________________AGCCGAGGAGAAC TCTGGCGCTGCATATTCTCCTG T EIF3H Ensembl:ENSG00000147677 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:116646537..116646650 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..52 33 SKCM 1 - Human_RBP_ID_5430032,Human_RBP_ID_5453001,Human_RBP_ID_5480550,Human_RBP_ID_5514182,Human_RBP_ID_7803235,Human_RBP_ID_17434001 Human_Splice_Rec_1002972,Human_Splice_Rec_1002986,Human_Splice_Rec_1003004,Human_Splice_Rec_1003012 RMVar_hsa_circ_2750,RMVar_hsa_circ_299166,RMVar_hsa_circ_55681,RMVar_hsa_circ_253978 115810 RMVar_ID_115810 Human_SNP_ID_875430106 m1A Human chr8 - 144517185 144517185 144517185 GGCCTGTGCCCCTGTTGTCTCCTGCAGGCGCCAGAGCCCCGCTGCTGGGGGCCCCATCTGAATCG GGCCTGTGCCCCTGTTGTCTCCTGCAGGCGCCTGAGCCCCGCTGCTGGGGGCCCCATCTGAATCG T A RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr8:144517022..144517282;chr8:144517066..144517200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_958356,Human_RBP_ID_5406288,Human_RBP_ID_18414332,Human_RBP_ID_19022503,Human_RBP_ID_22484077,Human_RBP_ID_22555713,Human_RBP_ID_22747717 Human_Splice_Rec_1024956,Human_Splice_Rec_1024994,Human_Splice_Rec_1025082,Human_Splice_Rec_1025090,Human_Splice_Rec_1025094 Human_miRNA_ID_2468855,Human_miRNA_ID_2756471 RMVar_hsa_circ_87253,RMVar_hsa_circ_255165 115811 RMVar_ID_115811 Human_SNP_ID_875502665 m1A Human chr8 - 33512339 33512339 33512339 ACTGGGGCAGGTAGCAAAAGCCCTGGAGAAGTATGCAGCCCCCTCCAAGGAGGAGGAAGGTGGAG ACTGGGGCAGGTAGCAAAAGCCCTGGAGAAGTGTGCAGCCCCCTCCAAGGAGGAGGAAGGTGGAG T C TTI2 Ensembl:ENSG00000129696 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:33512160..33512360 32194978 MeRIP-seq:(Medium) rs1306487105 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 8 prostate 115812 RMVar_ID_115812 Human_SNP_ID_875555492 m1A Human chr8 - 47961651 47961651 47961651 CACCTGAAGAATGCATTTGGGGAGGGCTGGAAAACAGCACGTCCTGCGCAGCAGGGCTCTGCAGG CACCTGAAGAATGCATTTGGGGAGGGCTGGAAGACAGCACGTCCTGCGCAGCAGGGCTCTGCAGG T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:47961601..47961650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck 115813 RMVar_ID_115813 Human_SNP_ID_875634466 m1A Human chr8 - 144512234 144512234 144512234 CAGCCCGGGGGACTTGACCGCTGAGGAGAAGGACCAGATATGTGACTTCCTCTATGGCCGTGTGC CAGCCCGGGGGACTTGACCGCTGAGGAGAAGGGCCAGATATGTGACTTCCTCTATGGCCGTGTGC T C RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144511387..144512516 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_18893778,Human_RBP_ID_23084163 Human_Splice_Rec_1024984,Human_Splice_Rec_1024985,Human_Splice_Rec_1025022,Human_Splice_Rec_1025023,Human_Splice_Rec_1025030,Human_Splice_Rec_1025031,Human_Splice_Rec_1025040,Human_Splice_Rec_1025041 Human_miRNA_ID_2248876 RMVar_hsa_circ_76649,RMVar_hsa_circ_92523,RMVar_hsa_circ_119980,RMVar_hsa_circ_255159,RMVar_hsa_circ_108923,RMVar_hsa_circ_255160,RMVar_hsa_circ_255161,RMVar_hsa_circ_255162 115814 RMVar_ID_115814 Human_SNP_ID_875663404 m1A Human chr8 - 98951696 98951696 98951696 GCGGCACGGGACAGATCCTGGGCTTCTCTAGAAGTCCTGCCGCGGGGTGTGAGTCAGGCTGTGCC GCGGCACGGGACAGATCCTGGGCTTCTCTAGACGTCCTGCCGCGGGGTGTGAGTCAGGCTGTGCC T G RF00017-4520,RF00017-4483,RF00017-4490 RNACentral:URS000099C2D3,RNACentral:URS000093C0AE,RNACentral:URS0000941A94 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:98951649..98951768 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 6 liver 115815 RMVar_ID_115815 Human_SNP_ID_875702730 m1A Human chr8 + 63038753 63038753 63038753 GCAGAGTAGCAGGCCCAGCACGCACAGCAGGCAGCCCGGACTGGCCATGGCGCTCGCCGCCTCCC GCAGAGTAGCAGGCCCAGCACGCACAGCAGGCGGCCCGGACTGGCCATGGCGCTCGCCGCCTCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr8:63038706..63038781;chr8:63038702..63038825 26863196 MeRIP-seq:(Medium) rs1800909 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,colon adenocarcinoma,COCA,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 6 caecum,liver,head and neck,large intestine GWAS_ID_12060,GWAS_ID_12061,GWAS_ID_12062,GWAS_ID_12063,GWAS_ID_12064,GWAS_ID_12065,GWAS_ID_12066,GWAS_ID_12067,GWAS_ID_12068 115816 RMVar_ID_115816 Human_SNP_ID_875779605 m1A Human chr8 - 22567171 22567171 22567171 CCCACTTGCTCTTGTCTCTCCTGCTCACCTCCACATAATTAGCAGGGAAGATGCCCAGGCGGCCG CCCACTTGCTCTTGTCTCTCCTGCTCACCTCCGCATAATTAGCAGGGAAGATGCCCAGGCGGCCG T C AC037459.3 Ensembl:ENSG00000254230 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:22567121..22567197 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 115817 RMVar_ID_115817 Human_SNP_ID_875797199 m1A Human chr8 - 38416027 38416027 38416027 TCCCTTGTATGTCATCGTGGAGTATGCCTCCAAGGGCAACCTGCGGGAGTACCTGCAGGCCCGGA TCCCTTGTATGTCATCGTGGAGTATGCCTCCAGGGGCAACCTGCGGGAGTACCTGCAGGCCCGGA T C FGFR1 Ensembl:ENSG00000077782 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38415976..38416075 32194978 MeRIP-seq:(Medium) rs531903077 Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 12 breast Human_RBP_ID_5534503,Human_RBP_ID_9405350,Human_RBP_ID_19021951 Human_Splice_Rec_966896,Human_Splice_Rec_966936,Human_Splice_Rec_966968,Human_Splice_Rec_966996,Human_Splice_Rec_967028,Human_Splice_Rec_967060,Human_Splice_Rec_967094,Human_Splice_Rec_967128,Human_Splice_Rec_967160,Human_Splice_Rec_967194,Human_Splice_Rec_967224,Human_Splice_Rec_967260,Human_Splice_Rec_967290,Human_Splice_Rec_967314,Human_Splice_Rec_967346,Human_Splice_Rec_967374,Human_Splice_Rec_967416,Human_Splice_Rec_967428,Human_Splice_Rec_967440,Human_Splice_Rec_967462 Human_miRNA_ID_2615156,Human_miRNA_ID_2615157,Human_miRNA_ID_2615158 RMVar_hsa_circ_1086,RMVar_hsa_circ_84323,RMVar_hsa_circ_369926,RMVar_hsa_circ_104175,RMVar_hsa_circ_100431,RMVar_hsa_circ_251424,RMVar_hsa_circ_77152,RMVar_hsa_circ_251426,RMVar_hsa_circ_251427,RMVar_hsa_circ_251425,RMVar_hsa_circ_251423,RMVar_hsa_circ_99803,RMVar_hsa_circ_251430 115818 RMVar_ID_115818 Human_SNP_ID_875810761 m1A Human chr8 + 143943692 143943692 143943692 TGCTTTCACTGACATTCAGCTTGGAAACAGGAAGGGGAGGGCGCAGGGAATGAAGGGGCGGGAGG TGCTTTCACTGACATTCAGCTTGGAAACAGGAGGGGGAGGGCGCAGGGAATGAAGGGGCGGGAGG A G RF00017-4575,RF00017-4518 RNACentral:URS0000918622,RNACentral:URS000098982A SRP RNA,SRP RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143943689..143943829 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115819 RMVar_ID_115819 Human_SNP_ID_875826458 m1A Human chr8 + 38424145 38424145 38424145 TTGCCAGAAAGATCGTACGTAACTCAGGACACAGGGCTAAGACTGGGAAACGCTTGGTGGAAAGG TTGCCAGAAAGATCGTACGTAACTCAGGACACTGGGCTAAGACTGGGAAACGCTTGGTGGAAAGG A T AC087623.1 Ensembl:ENSG00000255201 lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:38424144..38424295 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 115820 RMVar_ID_115820 Human_SNP_ID_875860417 m1A Human chr8 - 73976250 73976250 73976250 TCACGCGGGTGACGAGCGGCTGCGGACGCCCCAGCTGCACGAGTCCACGACTGCGAGACACGGCT TCACGCGGGTGACGAGCGGCTGCGGACGCCCCCGCTGCACGAGTCCACGACTGCGAGACACGGCT T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:73976201..73976375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 115821 RMVar_ID_115821 Human_SNP_ID_875883465 m1A Human chr8 - 107336261 107336261 107336261 TATTTTCATCTTTTATCTTAAGGTACTAAATCAAACTTCTCGACTTGAGATACAGCTGCTGGAGA TATTTTCATCTTTTATCTTAAGGTACTAAATCTAACTTCTCGACTTGAGATACAGCTGCTGGAGA T A ANGPT1 Ensembl:ENSG00000154188 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:107336222..107336299 26863196 MeRIP-seq:(Medium) rs772112333 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach Human_RBP_ID_957831 Human_Splice_Rec_1000596,Human_Splice_Rec_1000612,Human_Splice_Rec_1000626,Human_Splice_Rec_1000640 RMVar_hsa_circ_9672,RMVar_hsa_circ_82568,RMVar_hsa_circ_341247,RMVar_hsa_circ_362464,RMVar_hsa_circ_253848,RMVar_hsa_circ_253847,RMVar_hsa_circ_38575,RMVar_hsa_circ_64409,RMVar_hsa_circ_253849,RMVar_hsa_circ_316994 115822 RMVar_ID_115822 Human_SNP_ID_875904795 m1A Human chr8 + 13262634 13262634 13262634 CAGGCAGGAGTGCAGTGGCACAATCATAACTCACTTGCAGCCTTGAGCTCCTGGGCTCAAGTGAT CAGGCAGGAGTGCAGTGGCACAATCATAACTCGCTTGCAGCCTTGAGCTCCTGGGCTCAAGTGAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:13262627..13262757 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115823 RMVar_ID_115823 Human_SNP_ID_875922842 m1A Human chr8 - 41578276 41578276 41578276 GAGGTAAGGGGCCAGCTCCCTCCTACTCACCGACCGCGAGGCTAGGCAGCTCCAAATCCCGCGGC GAGGTAAGGGGCCAGCTCCCTCCTACTCACCGCCCGCGAGGCTAGGCAGCTCCAAATCCCGCGGC T G AC009630.1 Ensembl:ENSG00000253133 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:41578240..41578343 26863196 MeRIP-seq:(Medium) rs999188 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,central_nervous_system oligodendroglioma_Grade_III,liver hepatocellular_carcinoma,frontal_lobe oligodendroglioma_Grade_III 3 liver,brain GWAS_ID_15331,GWAS_ID_15332,GWAS_ID_15333,GWAS_ID_15334,GWAS_ID_15335,GWAS_ID_15336,GWAS_ID_15337,GWAS_ID_15338,GWAS_ID_15339,GWAS_ID_15340,GWAS_ID_15341,GWAS_ID_15342,GWAS_ID_15343,GWAS_ID_15344,GWAS_ID_15345,GWAS_ID_15346,GWAS_ID_15347,GWAS_ID_15348,GWAS_ID_15349,GWAS_ID_15350,GWAS_ID_15351,GWAS_ID_15352,GWAS_ID_15353,GWAS_ID_15354,GWAS_ID_15355,GWAS_ID_15356,GWAS_ID_15357,GWAS_ID_15358,GWAS_ID_15359,GWAS_ID_15360,GWAS_ID_15361,GWAS_ID_15362,GWAS_ID_15363 115824 RMVar_ID_115824 Human_SNP_ID_875948775 m1A Human chr8 - 219483 219483 219483 AATTAGGGACCAGGGTAGGGATCAGGATTTAGATTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG AATTAGGGACCAGGGTAGGGATCAGGATTTAGGTTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG T C RPL23AP53 Ensembl:ENSG00000223508 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:219480..219578 26863196 MeRIP-seq:(Medium) rs77316670 Functional Loss SNV ICGC 33..33 33 LAML 1 - 115825 RMVar_ID_115825 Human_SNP_ID_875948782 m1A Human chr8 - 219483 219483 219483 AATTAGGGACCAGGGTAGGGATCAGGATTTAGATTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG AATTAGGGACCAGGGTAGGGATCAGGATTTAGCTTCAGGGTCAAAGTCTTGGGACAGGGTTAGGG T G RPL23AP53 Ensembl:ENSG00000223508 Pseudogene intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:219480..219578 26863196 MeRIP-seq:(Medium) rs77316670 Functional Loss SNV ICGC 33..33 33 LUSC 2 - 115826 RMVar_ID_115826 Human_SNP_ID_875959415 m1A Human chr8 - 104588952 104588952 104588952 CGGCGGCGGCGGCGTCGGCGTCGTCTACCTCCAGCTTCTCCTCCCTCCTCCTCCGTCTCCTCCTC CGGCGGCGGCGGCGTCGGCGTCGTCTACCTCCGGCTTCTCCTCCCTCCTCCTCCGTCTCCTCCTC T C LRP12 Ensembl:ENSG00000147650 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:104588903..104589200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_4997161,Human_RBP_ID_18110850 Human_miRNA_ID_6981,Human_miRNA_ID_236453,Human_miRNA_ID_848175,Human_miRNA_ID_1386886 115827 RMVar_ID_115827 Human_SNP_ID_875979492 m1A Human chr8 + 26383130 26383130 26383130 TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACAATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC TGCTGCTGCCGCAGTCCTGCCAGCTGTCCGACGATGTCGTCCCACCTAGTCGAGCCGCCGCCGCC A G BNIP3L Ensembl:ENSG00000104765 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:26383079..26383327 26863196 MeRIP-seq:(Medium) rs1055479 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,oesophagus squamous_cell_carcinoma 6 oesophagus Human_RBP_ID_960751,Human_RBP_ID_4994953 GWAS_ID_13115,GWAS_ID_13116,GWAS_ID_13117,GWAS_ID_13118 RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 115828 RMVar_ID_115828 Human_SNP_ID_876040331 m1A Human chr8 + 66114246 66114246 66114246 GCTCGCTTAGCATGCGAGAGGTAGCGGGATCGATGCCCGCATCCTCCAGTTTTCCTTCCTGTCCC GCTCGCTTAGCATGCGAGAGGTAGCGGGATCGGTGCCCGCATCCTCCAGTTTTCCTTCCTGTCCC A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK293T cells, from four datasets;HEK-293T cells,m1A-quant-seq - 29072297,31548705 m1A-MAP&m1A-quant-seq:(High) rs1002540494 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115829 RMVar_ID_115829 Human_SNP_ID_876054481 m1A Human chr8 - 144428486 144428486 144428486 GCGCCATCTTCCCGACCGCGAGCCGTCCAGGTACCCGGGGCCCGGCCGGTGGGCGGGGAAGGGGC GCGCCATCTTCCCGACCGCGAGCCGTCCAGGTGCCCGGGGCCCGGCCGGTGGGCGGGGAAGGGGC T C VPS28 Ensembl:ENSG00000160948 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:144428476..144428550;chr8:144428476..144428525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_4995825,Human_RBP_ID_18427123,Human_RBP_ID_19142110 RMVar_hsa_circ_84676,RMVar_hsa_circ_255127 115830 RMVar_ID_115830 Human_SNP_ID_876069524 m1A Human chr8 - 28890877 28890877 28890877 CCTTTCCAGGACCGGACCCCACGAACTGCCCCACCCCACAGCCCGCGTCTGGGTCACCCACTCGG CCTTTCCAGGACCGGACCCCACGAACTGCCCCGCCCCACAGCCCGCGTCTGGGTCACCCACTCGG T C RF00017-4528,RF00017-4552 RNACentral:URS00009A4D01,RNACentral:URS0000973F83 SRP RNA,SRP RNA intron,intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr8:28890784..28890942 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115831 RMVar_ID_115831 Human_SNP_ID_876086815 m1A Human chr8 - 143696216 143696185 143696216 CCCACCCGACTCACGGCCCACCCACGCAACTCACGGCCCACCACGCAACTCACGGCCACCCACCC CCCACCCGACTCACGGCCCACCCACGCAACTC_______________________________CC GGTGGGTGGCCGTGAGTTGCGTGGTGGGCCGT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr8:143696104..143696402;chr8:143696099..143696399;chr8:143696115..143696404 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..63 33 LICA 1 - 115832 RMVar_ID_115832 Human_SNP_ID_876092201 m1A Human chr8 - 143818181 143818181 143818181 CTGGGGGGCAGGAACATCAAGGTGAGGCAGGGAGCCAAGGCCTCGATCCCGCAGGCGTGCAGGGC CTGGGGGGCAGGAACATCAAGGTGAGGCAGGGGGCCAAGGCCTCGATCCCGCAGGCGTGCAGGGC T C PUF60 Ensembl:ENSG00000179950 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143818176..143818275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LIHC 1 - Human_RBP_ID_5405037,Human_RBP_ID_19140477 RMVar_hsa_circ_126033,RMVar_hsa_circ_90248,RMVar_hsa_circ_92361,RMVar_hsa_circ_254954,RMVar_hsa_circ_254956,RMVar_hsa_circ_254955 115833 RMVar_ID_115833 Human_SNP_ID_876094666 m1A Human chr8 - 22367371 22367371 22367371 GCTCGGAGGCGGCCTCGGCCCCGCGCAGCCTCACCGCAAGGTCCCAGGCGGCCGGCGGCGGCAGA GCTCGGAGGCGGCCTCGGCCCCGCGCAGCCTCGCCGCAAGGTCCCAGGCGGCCGGCGGCGGCAGA T C RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:22367321..22367626 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115834 RMVar_ID_115834 Human_SNP_ID_876114977 m1A Human chr8 + 130443638 130443638 130443638 CGCGGCAGCGGCCAGGCCAGGCGAGGCGCGGGAGCCGAGCGCGGCGCAGGAAGGGGCGGGCGACC CGCGGCAGCGGCCAGGCCAGGCGAGGCGCGGGGGCCGAGCGCGGCGCAGGAAGGGGCGGGCGACC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr8:130443546..130443745 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115835 RMVar_ID_115835 Human_SNP_ID_876142663 m1A Human chr8 + 143307804 143307790 143307804 AGAGAAGAGGGCGGCAGAGGGTCCTGCGTGGCAGAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG AGAGAAGAGGGCGGCAGAG______________GAGAGGGCGGCAGAGGGTCCCGCGTGGCAGAG GGGTCCTGCGTGGCA G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143307717..143307841 26863196 MeRIP-seq:(Medium) rs369283627 Functional Loss DEL ICGC 20..33 33 PBCA 1 - 115836 RMVar_ID_115836 Human_SNP_ID_876157189 m1A Human chr8 - 143922787 143922787 143922787 CGAGCGGCAGCGGCAGCTGGAGATGAGCGCTGAGGCTGAGCGCCTCAAGCTGCGTGTGGCCGAGA CGAGCGGCAGCGGCAGCTGGAGATGAGCGCTGGGGCTGAGCGCCTCAAGCTGCGTGTGGCCGAGA T C PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143922092..143925600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_5534609 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_254969 115837 RMVar_ID_115837 Human_SNP_ID_876206576 m1A Human chr8 + 116847377 116847375 116847377 AATTTAATGTACTGGAAAAAAATGAAGAAGGAAAAAGGCAAAGACTTTGTACAGACAAAAATCTA AATTTAATGTACTGGAAAAAAATGAAGAAGG__AAAGGCAAAGACTTTGTACAGACAAAAATCTA GAA G UTP23 Ensembl:ENSG00000147679 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:116847332..116847483 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - 115838 RMVar_ID_115838 Human_SNP_ID_876260699 m1A Human chr8 + 60621869 60621869 60621869 GAAGGGGATATGACAATAAATCTATCAGATGGAAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA GAAGGGGATATGACAATAAATCTATCAGATGGGAAATCCTGTTACAAAGTAGAAAAGCTTTAGTA A G RAB2A Ensembl:ENSG00000104388 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7413 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_702173,Human_RBP_ID_3163413,Human_RBP_ID_26559228 GWAS_ID_11997,GWAS_ID_11998,GWAS_ID_11999,GWAS_ID_12000,GWAS_ID_12001,GWAS_ID_12002,GWAS_ID_12003,GWAS_ID_12004,GWAS_ID_12005,GWAS_ID_12006,GWAS_ID_12007,GWAS_ID_12008,GWAS_ID_12009,GWAS_ID_12010,GWAS_ID_12011,GWAS_ID_12012,GWAS_ID_12013,GWAS_ID_12014,GWAS_ID_12015,GWAS_ID_12016,GWAS_ID_12017,GWAS_ID_12018,GWAS_ID_12019,GWAS_ID_12020,GWAS_ID_12021,GWAS_ID_12022,GWAS_ID_12023,GWAS_ID_12024,GWAS_ID_12025,GWAS_ID_12026,GWAS_ID_12027,GWAS_ID_12028,GWAS_ID_12029,GWAS_ID_12030,GWAS_ID_12031,GWAS_ID_12032,GWAS_ID_12033,GWAS_ID_12034,GWAS_ID_12035,GWAS_ID_12036,GWAS_ID_12037,GWAS_ID_12038,GWAS_ID_12039,GWAS_ID_12040,GWAS_ID_12041,GWAS_ID_12042,GWAS_ID_12043,GWAS_ID_12044,GWAS_ID_12045,GWAS_ID_12046,GWAS_ID_12047,GWAS_ID_12048,GWAS_ID_12049,GWAS_ID_12050,GWAS_ID_12051,GWAS_ID_12052,GWAS_ID_12053,GWAS_ID_12054,GWAS_ID_12055,GWAS_ID_12056,GWAS_ID_12057,GWAS_ID_12058,GWAS_ID_12059 115839 RMVar_ID_115839 Human_SNP_ID_876290582 m1A Human chr8 - 38268986 38268986 38268986 TGCTCTGCGCTTCTTTGTTCCCCTCTAGGGTGACGGAGCTGCTCCCCCCGTTCCAGAGACTCATC TGCTCTGCGCTTCTTTGTTCCCCTCTAGGGTGGCGGAGCTGCTCCCCCCGTTCCAGAGACTCATC T C PLPP5 Ensembl:ENSG00000147535 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:38268936..38269015 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_958128,Human_RBP_ID_4984478,Human_RBP_ID_9406205,Human_RBP_ID_23120768 Human_Splice_Rec_966440,Human_Splice_Rec_966458,Human_Splice_Rec_966470,Human_Splice_Rec_966482,Human_Splice_Rec_966494,Human_Splice_Rec_966506,Human_Splice_Rec_966520,Human_Splice_Rec_966528 RMVar_hsa_circ_124664,RMVar_hsa_circ_92211,RMVar_hsa_circ_251397,RMVar_hsa_circ_251398 115840 RMVar_ID_115840 Human_SNP_ID_876291000 m1A Human chr8 - 142664651 142664651 142664651 CAGAGGTTGTGTGGAGTTCAGAAAAGACTCCGAAAGCTGACCAGGACGGCAGAGGAGATCCTGGT CAGAGGTTGTGTGGAGTTCAGAAAAGACTCCGGAAGCTGACCAGGACGGCAGAGGAGATCCTGGT T C JRK Ensembl:ENSG00000234616 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115841 RMVar_ID_115841 Human_SNP_ID_876324076 m1A Human chr8 - 143726510 143726510 143726510 GAGCCCCAAGGGCGAGCGGCGCATGGAGGATGAGGGTGGCTTCCCAGTGCCGCAGGAGAACGGCC GAGCCCCAAGGGCGAGCGGCGCATGGAGGATGTGGGTGGCTTCCCAGTGCCGCAGGAGAACGGCC T A FAM83H Ensembl:ENSG00000180921 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:143725668..143728986 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_695601,Human_RBP_ID_5534340,Human_RBP_ID_8917122 RMVar_hsa_circ_104177,RMVar_hsa_circ_120686,RMVar_hsa_circ_79039,RMVar_hsa_circ_98343,RMVar_hsa_circ_88604,RMVar_hsa_circ_254929,RMVar_hsa_circ_254931,RMVar_hsa_circ_254932,RMVar_hsa_circ_254933,RMVar_hsa_circ_254930 115842 RMVar_ID_115842 Human_SNP_ID_876347826 m1A Human chr8 + 90006313 90006313 90006313 TGTCCAGTTTTATGAGAGTGTTGTTGTTTGGTATATATCAAAGCTGAGACCTGAAAGATGAGTAG TGTCCAGTTTTATGAGAGTGTTGTTGTTTGGTGTATATCAAAGCTGAGACCTGAAAGATGAGTAG A G DECR1 Ensembl:ENSG00000104325 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:90006310..90006430 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_16831 115843 RMVar_ID_115843 Human_SNP_ID_876359929 m1A Human chr8 - 144096377 144096377 144096377 GGAAATAGTCGAACAGCTTCCCTGGCCGCATGAACATCTCCCCATCTTCATTGGGGCCGTCTTGA GGAAATAGTCGAACAGCTTCCCTGGCCGCATGGACATCTCCCCATCTTCATTGGGGCCGTCTTGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144096101..144096500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 115844 RMVar_ID_115844 Human_SNP_ID_876359935 m1A Human chr8 - 144096377 144096377 144096377 GGAAATAGTCGAACAGCTTCCCTGGCCGCATGAACATCTCCCCATCTTCATTGGGGCCGTCTTGA GGAAATAGTCGAACAGCTTCCCTGGCCGCATGTACATCTCCCCATCTTCATTGGGGCCGTCTTGA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:144096101..144096500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain 115845 RMVar_ID_115845 Human_SNP_ID_876364633 m1A Human chr8 - 109334401 109334401 109334401 AATGACCCTTGCGCTGAGGACCGTTACCTACCACACTCTTCGGCTGCCCGGACTTAGACCCTCAG AATGACCCTTGCGCTGAGGACCGTTACCTACCCCACTCTTCGGCTGCCCGGACTTAGACCCTCAG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:109334351..109334522 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 115846 RMVar_ID_115846 Human_SNP_ID_876364638 m1A Human chr8 - 109334401 109334401 109334401 AATGACCCTTGCGCTGAGGACCGTTACCTACCACACTCTTCGGCTGCCCGGACTTAGACCCTCAG AATGACCCTTGCGCTGAGGACCGTTACCTACCGCACTCTTCGGCTGCCCGGACTTAGACCCTCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:109334351..109334522 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 115847 RMVar_ID_115847 Human_SNP_ID_876386560 m1A Human chr8 - 143983718 143983718 143983718 GCCTCGGGAGCTGGAGGAGGAAGGGCCTCAGGAGCAGCCAGAGGAGGAGGTGACCCCAGGGCATG GCCTCGGGAGCTGGAGGAGGAAGGGCCTCAGGTGCAGCCAGAGGAGGAGGTGACCCCAGGGCATG T A PARP10 Ensembl:ENSG00000178685 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:143983516..143983809 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_8238904,Human_RBP_ID_19022275,Human_RBP_ID_23088064 Human_Splice_Rec_1022030,Human_Splice_Rec_1022050,Human_Splice_Rec_1022068,Human_Splice_Rec_1022088 115848 RMVar_ID_115848 Human_SNP_ID_876400046 m1A Human chr8 - 12746316 12746316 12746316 GTTGGGACTTTGAGTGAGTGGGAAGGTTCATAATGATAATTAAGGCTGGAGAGATGGGCAGGAGC GTTGGGACTTTGAGTGAGTGGGAAGGTTCATAGTGATAATTAAGGCTGGAGAGATGGGCAGGAGC T C LONRF1 Ensembl:ENSG00000154359 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:12746166..12746483 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_10384965,Human_RBP_ID_16346056 115849 RMVar_ID_115849 Human_SNP_ID_876427005 m1A Human chr8 + 140794499 140794499 140794499 GCCCTTGAATTCATTCTAATCAGTTCCCCCCCACCCCCATACACGGAAAATACTTTTTGAACATC GCCCTTGAATTCATTCTAATCAGTTCCCCCCCCCCCCCATACACGGAAAATACTTTTTGAACATC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:140794494..140794612 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115850 RMVar_ID_115850 Human_SNP_ID_876445364 m1A Human chr8 - 127794566 127794566 127794566 GGCCGCCCCGAGCCCGCCCGGCCCGCGGGCCCATGTGCTCGGCCGCCACACGCGCTCTGCCCGGA GGCCGCCCCGAGCCCGCCCGGCCCGCGGGCCCTTGTGCTCGGCCGCCACACGCGCTCTGCCCGGA T A lnc-FAM84B-8 RNACentral:URS00008BDA4B lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr8:127794526..127794670 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 115851 RMVar_ID_115851 Human_SNP_ID_876505201 m1A Human chr8 - 8228053 8228053 8228053 GCCGGGGCAGGGCGTTGACTATGTCGTACCACATGGCCAGGCGGTGCGCGGACTCTGGGAGGCGG GCCGGGGCAGGGCGTTGACTATGTCGTACCACCTGGCCAGGCGGTGCGCGGACTCTGGGAGGCGG T G FAM85B RNACentral:URS00008C2977 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:8228006..8228103 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 115852 RMVar_ID_115852 Human_SNP_ID_876506842 m1A Human chr8 - 30164137 30164137 30164137 TTACATCTCCTCTGATTTCACTTTCTACACATACAACTGCTCCAGGAGCAATCTTCACACTGTAG TTACATCTCCTCTGATTTCACTTTCTACACATGCAACTGCTCCAGGAGCAATCTTCACACTGTAG T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr8:30164087..30164217 26863410 MeRIP-seq:(Medium) rs750675730 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115853 RMVar_ID_115853 Human_SNP_ID_876522666 m1A Human chr8 - 144438729 144438727 144438730 CTGGGGTGGGCTTGGCTCTGTTCCAGAGGACGACACCGATGGCCTGACCCCGCAGCTGGAGGAGG CTGGGGTGGGCTTGGCTCTGTTCCAGAGGAC___ACCGATGGCCTGACCCCGCAGCTGGAGGAGG TGTC T TONSL Ensembl:ENSG00000160949 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144438651..144439924 26863196 MeRIP-seq:(Medium) rs778043482 Functional Loss DEL TCGA 32..34 33 ESCA 1 - Human_RBP_ID_3974367,Human_RBP_ID_19023487,Human_RBP_ID_26360288 Human_Splice_Rec_1024442,Human_Splice_Rec_1024443,Human_Splice_Rec_1024488,Human_Splice_Rec_1024489,Human_Splice_Rec_1024528,Human_Splice_Rec_1024529 RMVar_hsa_circ_63569,RMVar_hsa_circ_32773,RMVar_hsa_circ_56394,RMVar_hsa_circ_121664,RMVar_hsa_circ_62070,RMVar_hsa_circ_90150,RMVar_hsa_circ_112340,RMVar_hsa_circ_255132,RMVar_hsa_circ_255133,RMVar_hsa_circ_118426,RMVar_hsa_circ_255134,RMVar_hsa_circ_27518,RMVar_hsa_circ_120640,RMVar_hsa_circ_255135,RMVar_hsa_circ_86507,RMVar_hsa_circ_255136,RMVar_hsa_circ_100768,RMVar_hsa_circ_255137,RMVar_hsa_circ_45558,RMVar_hsa_circ_255138,RMVar_hsa_circ_77815,RMVar_hsa_circ_24346,RMVar_hsa_circ_255139 115854 RMVar_ID_115854 Human_SNP_ID_876527297 m1A Human chr8 + 38972530 38972530 38972530 TGTAGTTCAATATGAGATAAATTATTATCTTCAATGAAACAAGCTCTAAAAGCATTCCATTCCTA TGTAGTTCAATATGAGATAAATTATTATCTTCGATGAAACAAGCTCTAAAAGCATTCCATTCCTA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7001984 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,liver hepatocellular_carcinoma 2 liver RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 115855 RMVar_ID_115855 Human_SNP_ID_876530197 m1A Human chr8 - 144512744 144512744 144512744 CCCAGCCATCGAGACTTTGCTGTGCTACCTGGAGCTGCACCCACACCACTGGCTGGAGCTGCTGG CCCAGCCATCGAGACTTTGCTGTGCTACCTGGCGCTGCACCCACACCACTGGCTGGAGCTGCTGG T G RECQL4 Ensembl:ENSG00000160957 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144512694..144513084 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_959690,Human_RBP_ID_1054715,Human_RBP_ID_1335222,Human_RBP_ID_3974388,Human_RBP_ID_5405156,Human_RBP_ID_16382457,Human_RBP_ID_17544775,Human_RBP_ID_18172597,Human_RBP_ID_18893783,Human_RBP_ID_19022495,Human_RBP_ID_23088162,Human_RBP_ID_23216401,Human_RBP_ID_26358774 Human_Splice_Rec_1024980,Human_Splice_Rec_1025018,Human_Splice_Rec_1025062 Human_miRNA_ID_2012531,Human_miRNA_ID_2758905,Human_miRNA_ID_3006718 RMVar_hsa_circ_76649,RMVar_hsa_circ_92523,RMVar_hsa_circ_255159,RMVar_hsa_circ_255163,RMVar_hsa_circ_108923,RMVar_hsa_circ_255160,RMVar_hsa_circ_299016,RMVar_hsa_circ_255162,RMVar_hsa_circ_255164,RMVar_hsa_circ_279366 115856 RMVar_ID_115856 Human_SNP_ID_876592084 m1A Human chr8 - 27748149 27748149 27748149 ATGCAGAGATCGTGAAGAGAGGAATGAGAAAAAAGCCCAAATTCAGGAAATGAAAAAGAGAGAAA ATGCAGAGATCGTGAAGAGAGGAATGAGAAAACAGCCCAAATTCAGGAAATGAAAAAGAGAGAAA T G CCDC25 Ensembl:ENSG00000147419 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:27748056..27748250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_4981286,Human_RBP_ID_9223732,Human_RBP_ID_18116688,Human_RBP_ID_24254433,Human_RBP_ID_27831754 Human_Splice_Rec_961393,Human_Splice_Rec_961407,Human_Splice_Rec_961419,Human_Splice_Rec_961433,Human_Splice_Rec_961445,Human_Splice_Rec_961457,Human_Splice_Rec_961461 RMVar_hsa_circ_27342,RMVar_hsa_circ_328808,RMVar_hsa_circ_359028,RMVar_hsa_circ_335705,RMVar_hsa_circ_312928,RMVar_hsa_circ_250961 115857 RMVar_ID_115857 Human_SNP_ID_876593447 m1A Human chr8 - 99892049 99892049 99892049 ACTTAATCATATTTTCTGAATCTCTTAAGGTTAGCATACGTATCAAGGACAGTAACTACCATGGC ACTTAATCATATTTTCTGAATCTCTTAAGGTTGGCATACGTATCAAGGACAGTAACTACCATGGC T C COX6C Ensembl:ENSG00000164919 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:99892026..99892075 26863196 MeRIP-seq:(Medium) rs1130474 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 17 haematopoietic and lymphoid tissue Human_RBP_ID_4995649,Human_RBP_ID_5328881,Human_RBP_ID_9338316,Human_RBP_ID_16297302,Human_RBP_ID_22464978,Human_RBP_ID_23216163 Human_Splice_Rec_996736,Human_Splice_Rec_996744,Human_Splice_Rec_996752,Human_Splice_Rec_996764,Human_Splice_Rec_996776,Human_Splice_Rec_996782,Human_Splice_Rec_996788,Human_Splice_Rec_996794 RMVar_hsa_circ_61370,RMVar_hsa_circ_315033 115858 RMVar_ID_115858 Human_SNP_ID_876600561 m1A Human chr8 - 120445097 120445097 120445097 AGGAGAAGGACGTACGGTCCTGCTAGTAGAGGAATATGTCGAGTTTCTCTAGGGCGCCCCAGGTG AGGAGAAGGACGTACGGTCCTGCTAGTAGAGGGATATGTCGAGTTTCTCTAGGGCGCCCCAGGTG T C MRPL13 Ensembl:ENSG00000172172 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:120445006..120445098 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney Human_RBP_ID_706945,Human_RBP_ID_4995686,Human_RBP_ID_5328906,Human_RBP_ID_8678882,Human_RBP_ID_16336926,Human_RBP_ID_24243552 Human_Splice_Rec_1004505,Human_Splice_Rec_1004517,Human_Splice_Rec_1004541 115859 RMVar_ID_115859 Human_SNP_ID_876612553 m1A Human chr8 - 143927985 143927985 143927985 GCCCTGAGCCCCGCTTTCCCGCCAGGCTCAAGACCATCAGCCTGGTGATCCGCGGCACGCAGGGG GCCCTGAGCCCCGCTTTCCCGCCAGGCTCAAGCCCATCAGCCTGGTGATCCGCGGCACGCAGGGG T G PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr8:143927851..143928000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 10 pancreas Human_RBP_ID_89163,Human_RBP_ID_3973433,Human_RBP_ID_5405554,Human_RBP_ID_5534430,Human_RBP_ID_19023217,Human_RBP_ID_22115228,Human_RBP_ID_22688613,Human_RBP_ID_23259515,Human_RBP_ID_27536746,Human_RBP_ID_27569710 Human_Splice_Rec_1021388,Human_Splice_Rec_1021448,Human_Splice_Rec_1021508,Human_Splice_Rec_1021568,Human_Splice_Rec_1021628,Human_Splice_Rec_1021688,Human_Splice_Rec_1021748,Human_Splice_Rec_1021808,Human_Splice_Rec_1021868,Human_Splice_Rec_1021926 RMVar_hsa_circ_80124,RMVar_hsa_circ_115534,RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254970,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968,RMVar_hsa_circ_125399,RMVar_hsa_circ_379061,RMVar_hsa_circ_348791,RMVar_hsa_circ_254969,RMVar_hsa_circ_372182,RMVar_hsa_circ_99901,RMVar_hsa_circ_105338,RMVar_hsa_circ_105904,RMVar_hsa_circ_103649,RMVar_hsa_circ_85553,RMVar_hsa_circ_81244,RMVar_hsa_circ_254972,RMVar_hsa_circ_254976,RMVar_hsa_circ_254978,RMVar_hsa_circ_254979,RMVar_hsa_circ_254977,RMVar_hsa_circ_254974,RMVar_hsa_circ_254975,RMVar_hsa_circ_254973,RMVar_hsa_circ_103540,RMVar_hsa_circ_254971,RMVar_hsa_circ_254982 115860 RMVar_ID_115860 Human_SNP_ID_876630087 m1A Human chr8 + 144501652 144501652 144501652 AGCTGAGCCCCCTGGACAGCACCACCCCCCACACCCTGGTCCACGACAAGGCCCACCACACCCTG AGCTGAGCCCCCTGGACAGCACCACCCCCCACCCCCTGGTCCACGACAAGGCCCACCACACCCTG A C PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:144501602..144501800 26863196 MeRIP-seq:(Medium) rs961726379 Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 2 uterus Human_RBP_ID_17666053,Human_RBP_ID_27536915 RMVar_hsa_circ_75820,RMVar_hsa_circ_92666,RMVar_hsa_circ_83124,RMVar_hsa_circ_255147,RMVar_hsa_circ_255148,RMVar_hsa_circ_122780,RMVar_hsa_circ_255149,RMVar_hsa_circ_255153 115861 RMVar_ID_115861 Human_SNP_ID_876655358 m1A Human chr8 + 54135300 54135300 54135300 CTTGGATCTGCGGGTTATGGCCGGTCCCTTGCAGGGCGGTGGGGCCCGGGCCCTGGACCTACTCC CTTGGATCTGCGGGTTATGGCCGGTCCCTTGCGGGGCGGTGGGGCCCGGGCCCTGGACCTACTCC A G MRPL15 Ensembl:ENSG00000137547 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:54135250..54135425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_255344,Human_RBP_ID_701243,Human_RBP_ID_796812,Human_RBP_ID_4995053,Human_RBP_ID_18426696,Human_RBP_ID_22464944 Human_Splice_Rec_978209,Human_Splice_Rec_978217 115862 RMVar_ID_115862 Human_SNP_ID_876669573 m1A Human chr8 - 142736085 142736082 142736085 AGGCTACCCTCCCGTCCAGCCTGACTGGAGGTAGAGGAGGAGGAGGAGGCAAGGCCGACTGCAGT AGGCTACCCTCCCGTCCAGCCTGACTGGAGGT___GGAGGAGGAGGAGGCAAGGCCGACTGCAGT CTCT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:142735976..142736350 32194978 MeRIP-seq:(Medium) rs1233280862 Functional Loss DEL TCGA 33..35 33 CESC 1 - 115863 RMVar_ID_115863 Human_SNP_ID_876718686 m1A Human chr8 - 144791386 144791380 144791386 CCTGGAGACCGTGGCAAGCTGGCCCGGGCATCAGGGAACTATGCCACCGTTATCTCCCACAACCC CCTGGAGACCGTGGCAAGCTGGCCCGGGCATC______CTATGCCACCGTTATCTCCCACAACCC GTTCCCT G RPL8 Ensembl:ENSG00000161016 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr8:144791242..144791528 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..38 33 STAD 1 - Human_RBP_ID_254983,Human_RBP_ID_696107,Human_RBP_ID_959921,Human_RBP_ID_1054734,Human_RBP_ID_1694332,Human_RBP_ID_2053541,Human_RBP_ID_3874921,Human_RBP_ID_4998865,Human_RBP_ID_7818500,Human_RBP_ID_8917391,Human_RBP_ID_9222160,Human_RBP_ID_16384825,Human_RBP_ID_17666060,Human_RBP_ID_18196690,Human_RBP_ID_22465747,Human_RBP_ID_22516780,Human_RBP_ID_22534454,Human_RBP_ID_23140702,Human_RBP_ID_27774513 Human_Splice_Rec_1025357 Human_miRNA_ID_2958989,Human_miRNA_ID_2958990,Human_miRNA_ID_3001222,Human_miRNA_ID_3001223 RMVar_hsa_circ_8309,RMVar_hsa_circ_82581,RMVar_hsa_circ_119399,RMVar_hsa_circ_82967,RMVar_hsa_circ_255180,RMVar_hsa_circ_77055,RMVar_hsa_circ_80417,RMVar_hsa_circ_255182,RMVar_hsa_circ_255183,RMVar_hsa_circ_255181,RMVar_hsa_circ_255179,RMVar_hsa_circ_14057,RMVar_hsa_circ_97186,RMVar_hsa_circ_255188,RMVar_hsa_circ_95715,RMVar_hsa_circ_255187 115864 RMVar_ID_115864 Human_SNP_ID_876772295 m1A Human chr8 + 143992350 143992350 143992350 TGGCCGTGGGCATCACCACAGCCGTCTGCTTCACCGTCGTCATCTTCTCCATGCAGGTGAGGGGC TGGCCGTGGGCATCACCACAGCCGTCTGCTTCTCCGTCGTCATCTTCTCCATGCAGGTGAGGGGC A T GRINA Ensembl:ENSG00000178719 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr8:143992301..143992379 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 2 breast Human_RBP_ID_5225195,Human_RBP_ID_8682983,Human_RBP_ID_17434070,Human_RBP_ID_21564992,Human_RBP_ID_22775772,Human_RBP_ID_27536763 Human_Splice_Rec_1022197,Human_Splice_Rec_1022209,Human_Splice_Rec_1022229,Human_Splice_Rec_1022235,Human_Splice_Rec_1022241,Human_Splice_Rec_1022249,Human_Splice_Rec_1022253 RMVar_hsa_circ_91055,RMVar_hsa_circ_119657,RMVar_hsa_circ_255000,RMVar_hsa_circ_115447,RMVar_hsa_circ_99170,RMVar_hsa_circ_255002,RMVar_hsa_circ_110572,RMVar_hsa_circ_255004,RMVar_hsa_circ_96301,RMVar_hsa_circ_255005,RMVar_hsa_circ_113440,RMVar_hsa_circ_255006,RMVar_hsa_circ_255008,RMVar_hsa_circ_1200,RMVar_hsa_circ_255007 115865 RMVar_ID_115865 Human_SNP_ID_876839851 m1A Human chr8 - 143919352 143919352 143919352 CAGCCACCGCGTGCCTGTGGACGTGGCCTACCAGCGCGGCTACTTCAGTGAGGAGATGAACCGCG CAGCCACCGCGTGCCTGTGGACGTGGCCTACCTGCGCGGCTACTTCAGTGAGGAGATGAACCGCG T A PLEC Ensembl:ENSG00000178209 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr8:143919051..143919645 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_89137,Human_RBP_ID_8917300,Human_RBP_ID_26832476 RMVar_hsa_circ_106694,RMVar_hsa_circ_116096,RMVar_hsa_circ_254967,RMVar_hsa_circ_254968 115866 RMVar_ID_115866 Human_SNP_ID_876885089 m1A Human chr8 + 144096449 144096449 144096449 ATACCCCAACAGTGAGGCTGCTCGAGCTGCCAACAACGGAGCATTGCCCCCTGACCTCAGCTACA ATACCCCAACAGTGAGGCTGCTCGAGCTGCCACCAACGGAGCATTGCCCCCTGACCTCAGCTACA A C CYC1 Ensembl:ENSG00000179091 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:144096323..144096490 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck Human_RBP_ID_695781,Human_RBP_ID_1694094,Human_RBP_ID_4974711,Human_RBP_ID_8683016,Human_RBP_ID_27122359 Human_Splice_Rec_1022517,Human_Splice_Rec_1022529 RMVar_hsa_circ_5289,RMVar_hsa_circ_107093,RMVar_hsa_circ_90969,RMVar_hsa_circ_255022,RMVar_hsa_circ_110052,RMVar_hsa_circ_255023,RMVar_hsa_circ_372537,RMVar_hsa_circ_255024,RMVar_hsa_circ_116008,RMVar_hsa_circ_92432,RMVar_hsa_circ_255025,RMVar_hsa_circ_255026,RMVar_hsa_circ_255027 115867 RMVar_ID_115867 Human_SNP_ID_876942897 m1A Human chr8 + 23309843 23309843 23309843 GCAGTTCTCCTCCATGGCACACTGCAGCATGAACATGGGCCGGTCCTCCAGGTAGGTGGTCTGCT GCAGTTCTCCTCCATGGCACACTGCAGCATGAGCATGGGCCGGTCCTCCAGGTAGGTGGTCTGCT A G RF00017-4488 RNACentral:URS0000993263 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr8:23298901..23316779 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 115868 RMVar_ID_115868 Human_SNP_ID_876949666 m1A Human chr8 + 21984702 21984702 21984702 GGATACGGGGCTGGTCCAGCAGCAGTTGGACCAGCTGTCCACCATTGGGCGTTGTGAATATGAGA GGATACGGGGCTGGTCCAGCAGCAGTTGGACCTGCTGTCCACCATTGGGCGTTGTGAATATGAGA A T XPO7 Ensembl:ENSG00000130227 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr8:21981749..21984825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_1054962,Human_RBP_ID_8917964,Human_RBP_ID_9312495,Human_RBP_ID_22464852 Human_Splice_Rec_954998,Human_Splice_Rec_955080 RMVar_hsa_circ_5827,RMVar_hsa_circ_85039,RMVar_hsa_circ_250593,RMVar_hsa_circ_119137,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,RMVar_hsa_circ_250595,RMVar_hsa_circ_310810,RMVar_hsa_circ_324883,RMVar_hsa_circ_102919,RMVar_hsa_circ_110518,RMVar_hsa_circ_250599,RMVar_hsa_circ_250600,RMVar_hsa_circ_377779,RMVar_hsa_circ_116142,RMVar_hsa_circ_92609,RMVar_hsa_circ_95030,RMVar_hsa_circ_87858,RMVar_hsa_circ_250603,RMVar_hsa_circ_250605,RMVar_hsa_circ_250606,RMVar_hsa_circ_250604,RMVar_hsa_circ_30353,RMVar_hsa_circ_250601,RMVar_hsa_circ_250602,RMVar_hsa_circ_94423,RMVar_hsa_circ_107623,RMVar_hsa_circ_250613,RMVar_hsa_circ_250614,RMVar_hsa_circ_44806,RMVar_hsa_circ_321844,RMVar_hsa_circ_361382,RMVar_hsa_circ_370837,RMVar_hsa_circ_250615,RMVar_hsa_circ_364028,RMVar_hsa_circ_349572,RMVar_hsa_circ_293237,RMVar_hsa_circ_60352,RMVar_hsa_circ_119847,RMVar_hsa_circ_33877,RMVar_hsa_circ_85146,RMVar_hsa_circ_82787,RMVar_hsa_circ_250618,RMVar_hsa_circ_250620,RMVar_hsa_circ_250619,RMVar_hsa_circ_250616,RMVar_hsa_circ_250617,RMVar_hsa_circ_250623,RMVar_hsa_circ_250624,RMVar_hsa_circ_88291,RMVar_hsa_circ_250626,RMVar_hsa_circ_366982,RMVar_hsa_circ_110972,RMVar_hsa_circ_92023,RMVar_hsa_circ_250628,RMVar_hsa_circ_250630,RMVar_hsa_circ_250629,RMVar_hsa_circ_250627,RMVar_hsa_circ_101216,RMVar_hsa_circ_80018,RMVar_hsa_circ_91053,RMVar_hsa_circ_250634,RMVar_hsa_circ_250635,RMVar_hsa_circ_250637,RMVar_hsa_circ_80679,RMVar_hsa_circ_250636,RMVar_hsa_circ_96001,RMVar_hsa_circ_250638,RMVar_hsa_circ_250639 115869 RMVar_ID_115869 Human_SNP_ID_876955758 m1A Human chr8 - 143986406 143986406 143986406 CAGGGTTAGGCTTGCTGAGGGGCAGGCACAGGAGTCCTGGCTGAGCTCATGGCCTGAGGCTGCCT CAGGGTTAGGCTTGCTGAGGGGCAGGCACAGGGGTCCTGGCTGAGCTCATGGCCTGAGGCTGCCT T C PARP10 Ensembl:ENSG00000178685 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143986325..143986450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_4996431 Human_Splice_Rec_1022017,Human_Splice_Rec_1022037,Human_Splice_Rec_1022075,Human_Splice_Rec_1022099,Human_Splice_Rec_1022105,Human_Splice_Rec_1022114,Human_Splice_Rec_1022115,Human_Splice_Rec_1022122,Human_Splice_Rec_1022123,Human_Splice_Rec_1022130,Human_Splice_Rec_1022131,Human_Splice_Rec_1022136,Human_Splice_Rec_1022137,Human_Splice_Rec_1022142,Human_Splice_Rec_1022143,Human_Splice_Rec_1022148,Human_Splice_Rec_1022149,Human_Splice_Rec_1022154,Human_Splice_Rec_1022155,Human_Splice_Rec_1022160,Human_Splice_Rec_1022161,Human_Splice_Rec_1022165,Human_Splice_Rec_1022168,Human_Splice_Rec_1022169,Human_Splice_Rec_1022174,Human_Splice_Rec_1022175,Human_Splice_Rec_1022180,Human_Splice_Rec_1022181,Human_Splice_Rec_1022186,Human_Splice_Rec_1022188 115870 RMVar_ID_115870 Human_SNP_ID_877018734 m1A Human chr8 + 143816731 143816731 143816731 CTTGGTAGATGATGACGCGGTTCACGGCCCCGAACTTGCCACACTCCTCTGTCACCTCCCCTTCC CTTGGTAGATGATGACGCGGTTCACGGCCCCGGACTTGCCACACTCCTCTGTCACCTCCCCTTCC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr8:143816376..143816819 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - 115871 RMVar_ID_115871 Human_SNP_ID_813954761 m1A Human chr12 - 12549343 12549343 12549343 GTGCGGGGGTGGGTGCAACAGGAGTCATGGAGATGCACATATAATTGAAGGATTTCCATCAAAAC GTGCGGGGGTGGGTGCAACAGGAGTCATGGAGTTGCACATATAATTGAAGGATTTCCATCAAAAC T A DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:12549336..12549463 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_2312684 RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 115872 RMVar_ID_115872 Human_SNP_ID_813990728 m1A Human chr12 - 132775209 132775209 132775209 TGCTCCAGGCAAAAGTGTCGGAGCTGAAGAACAACATGAAGACCCTGCTCCAGCAGAACCAGCAG TGCTCCAGGCAAAAGTGTCGGAGCTGAAGAACCACATGAAGACCCTGCTCCAGCAGAACCAGCAG T G GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132775111..132775218 26863196 MeRIP-seq:(Medium) rs779002581 Functional Loss SNV TCGA 33..33 33 BLCA 1 - Human_RBP_ID_990950,Human_RBP_ID_1791188,Human_RBP_ID_5111857,Human_RBP_ID_9255632,Human_RBP_ID_9280017,Human_RBP_ID_9365958,Human_RBP_ID_11884356 Human_Splice_Rec_1447240,Human_Splice_Rec_1447241,Human_Splice_Rec_1447286,Human_Splice_Rec_1447287,Human_Splice_Rec_1447292,Human_Splice_Rec_1447338 RMVar_hsa_circ_82224,RMVar_hsa_circ_76294,RMVar_hsa_circ_111370,RMVar_hsa_circ_161875,RMVar_hsa_circ_19413,RMVar_hsa_circ_161877,RMVar_hsa_circ_161878,RMVar_hsa_circ_63608,RMVar_hsa_circ_268857,RMVar_hsa_circ_340011 115873 RMVar_ID_115873 Human_SNP_ID_814011371 m1A Human chr12 - 57547140 57547140 57547140 TCCCTTTGCCGCCGCCTTAGCCCGGGACCCGAACCCAGCCTCTCCCCTACCCGAACACCGGCCCC TCCCTTTGCCGCCGCCTTAGCCCGGGACCCGACCCCAGCCTCTCCCCTACCCGAACACCGGCCCC T G DCTN2 Ensembl:ENSG00000175203 Protein coding 5'UTR GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584;GSE70485:GSM1972531,GSM1972532 HEK293T,untreat control;HEPG2 cell line,mRNA heat shock 4h chr12:57547054..57547162;chr12:57547026..57547232 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_424818,Human_RBP_ID_754262,Human_RBP_ID_811314,Human_RBP_ID_5437893,Human_RBP_ID_5462015,Human_RBP_ID_22436032 RMVar_hsa_circ_100953,RMVar_hsa_circ_157682 115874 RMVar_ID_115874 Human_SNP_ID_814020512 m1A Human chr12 + 53985240 53985239 53985240 ATGTCAGCTCCTCCGCTGTAGTATTGCTCCTTAAAAACCCCTCTCTCTGAAAATGACATGCCCTC ATGTCAGCTCCTCCGCTGTAGTATTGCTCCTT_AAAACCCCTCTCTCTGAAAATGACATGCCCTC TA T HOXC10 Ensembl:ENSG00000180818 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53985190..53985349 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 33..33 33 STAD 2 - Human_RBP_ID_5417119,Human_RBP_ID_5437799 115875 RMVar_ID_115875 Human_SNP_ID_814023646 m1A Human chr12 + 69586320 69586319 69586321 CCTGTTAACATCTTTAAGGCAGGAGCTGATGAAGAGAGAGCAGAGACAGCTCGTCTGGTAAGCCT CCTGTTAACATCTTTAAGGCAGGAGCTGATGA__AGAGAGCAGAGACAGCTCGTCTGGTAAGCCT AAG A CCT2 Ensembl:ENSG00000166226 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:69586239..69586386 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 STAD 1 - Human_RBP_ID_753982,Human_RBP_ID_810804,Human_RBP_ID_876915,Human_RBP_ID_1477064,Human_RBP_ID_1800670,Human_RBP_ID_3941983,Human_RBP_ID_4246853,Human_RBP_ID_5349923,Human_RBP_ID_18977611,Human_RBP_ID_22437923,Human_RBP_ID_25000252,Human_RBP_ID_26911328 Human_Splice_Rec_1396780,Human_Splice_Rec_1396781,Human_Splice_Rec_1396788,Human_Splice_Rec_1396789,Human_Splice_Rec_1396792,Human_Splice_Rec_1396793,Human_Splice_Rec_1396798,Human_Splice_Rec_1396799,Human_Splice_Rec_1396808,Human_Splice_Rec_1396809,Human_Splice_Rec_1396820,Human_Splice_Rec_1396821,Human_Splice_Rec_1396852,Human_Splice_Rec_1396853,Human_Splice_Rec_1396856,Human_Splice_Rec_1396857,Human_Splice_Rec_1396884,Human_Splice_Rec_1396885,Human_Splice_Rec_1396912,Human_Splice_Rec_1396913 RMVar_hsa_circ_11638,RMVar_hsa_circ_113475,RMVar_hsa_circ_158187,RMVar_hsa_circ_82498,RMVar_hsa_circ_158186 115876 RMVar_ID_115876 Human_SNP_ID_814026716 m1A Human chr12 - 50016718 50016718 50016718 GACCCCTAATGTATATTTGATTTCTTGGCAGAAAGATGGATACTATGATGCTGAATGTGCGGAAT GACCCCTAATGTATATTTGATTTCTTGGCAGACAGATGGATACTATGATGCTGAATGTGCGGAAT T G RACGAP1 Ensembl:ENSG00000161800 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:50016626..50016958 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_11960137,Human_RBP_ID_22572532,Human_RBP_ID_23562594 Human_Splice_Rec_1367142,Human_Splice_Rec_1367143,Human_Splice_Rec_1367174,Human_Splice_Rec_1367175,Human_Splice_Rec_1367206,Human_Splice_Rec_1367207,Human_Splice_Rec_1367237,Human_Splice_Rec_1367272,Human_Splice_Rec_1367273,Human_Splice_Rec_1367336,Human_Splice_Rec_1367337,Human_Splice_Rec_1367349,Human_Splice_Rec_1367370,Human_Splice_Rec_1367371,Human_Splice_Rec_1367382,Human_Splice_Rec_1367383,Human_Splice_Rec_1367411,Human_Splice_Rec_1367421,Human_Splice_Rec_1367431,Human_Splice_Rec_1367439,Human_Splice_Rec_1367446,Human_Splice_Rec_1367447,Human_Splice_Rec_1367460,Human_Splice_Rec_1367461,Human_Splice_Rec_1367466,Human_Splice_Rec_1367467,Human_Splice_Rec_1367472,Human_Splice_Rec_1367473,Human_Splice_Rec_1367480,Human_Splice_Rec_1367481,Human_Splice_Rec_1367488,Human_Splice_Rec_1367489,Human_Splice_Rec_1367497 Human_miRNA_ID_3063023 RMVar_hsa_circ_77098,RMVar_hsa_circ_125613,RMVar_hsa_circ_38912,RMVar_hsa_circ_68956,RMVar_hsa_circ_156379,RMVar_hsa_circ_312022,RMVar_hsa_circ_53776,RMVar_hsa_circ_156381,RMVar_hsa_circ_156380,RMVar_hsa_circ_43019,RMVar_hsa_circ_56485,RMVar_hsa_circ_32453,RMVar_hsa_circ_24576,RMVar_hsa_circ_356050,RMVar_hsa_circ_156394,RMVar_hsa_circ_101053,RMVar_hsa_circ_334636,RMVar_hsa_circ_117200,RMVar_hsa_circ_156396,RMVar_hsa_circ_156397,RMVar_hsa_circ_332903,RMVar_hsa_circ_156398,RMVar_hsa_circ_298346 115877 RMVar_ID_115877 Human_SNP_ID_814040598 m1A Human chr12 - 53714668 53714668 53714668 CCCTCAGGTACAGTTGTCAGAAAGTAAGCGGGAGCTGACAGAGCTGCGGTCAGCCCTGCGTGTGC CCCTCAGGTACAGTTGTCAGAAAGTAAGCGGGGGCTGACAGAGCTGCGGTCAGCCCTGCGTGTGC T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:53714557..53714700;chr12:53714565..53714709 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_3942999,Human_RBP_ID_8229879,Human_RBP_ID_26321466 Human_Splice_Rec_1376362,Human_Splice_Rec_1376363,Human_Splice_Rec_1376390,Human_Splice_Rec_1376391,Human_Splice_Rec_1376399,Human_Splice_Rec_1376426,Human_Splice_Rec_1376427,Human_Splice_Rec_1376454,Human_Splice_Rec_1376455,Human_Splice_Rec_1376480,Human_Splice_Rec_1376481,Human_Splice_Rec_1376488,Human_Splice_Rec_1376489 115878 RMVar_ID_115878 Human_SNP_ID_814040601 m1A Human chr12 - 53714668 53714668 53714668 CCCTCAGGTACAGTTGTCAGAAAGTAAGCGGGAGCTGACAGAGCTGCGGTCAGCCCTGCGTGTGC CCCTCAGGTACAGTTGTCAGAAAGTAAGCGGGCGCTGACAGAGCTGCGGTCAGCCCTGCGTGTGC T G CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:53714557..53714700;chr12:53714565..53714709 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_3942999,Human_RBP_ID_8229879,Human_RBP_ID_26321466 Human_Splice_Rec_1376362,Human_Splice_Rec_1376363,Human_Splice_Rec_1376390,Human_Splice_Rec_1376391,Human_Splice_Rec_1376399,Human_Splice_Rec_1376426,Human_Splice_Rec_1376427,Human_Splice_Rec_1376454,Human_Splice_Rec_1376455,Human_Splice_Rec_1376480,Human_Splice_Rec_1376481,Human_Splice_Rec_1376488,Human_Splice_Rec_1376489 115879 RMVar_ID_115879 Human_SNP_ID_814044329 m1A Human chr12 + 64450291 64450291 64450291 CTCCTGCCTCAGCATCCAGACTAGCTGTGATTACAGGTGTGCACCACCACACCCAGCTACATTTT CTCCTGCCTCAGCATCCAGACTAGCTGTGATTGCAGGTGTGCACCACCACACCCAGCTACATTTT A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26418882 Human_miRNA_ID_1398895 115880 RMVar_ID_115880 Human_SNP_ID_814056701 m1A Human chr12 - 56116661 56116661 56116661 CGGAATCCCAACGCAGGAACCAAAAAACACTCACCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG CGGAATCCCAACGCAGGAACCAAAAAACACTCGCCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56116626..56116675 32194978 MeRIP-seq:(Medium) rs987428401 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,UCEC,large_intestine adenocarcinoma 5 caecum,large intestine 115881 RMVar_ID_115881 Human_SNP_ID_814056706 m1A Human chr12 - 56116661 56116661 56116661 CGGAATCCCAACGCAGGAACCAAAAAACACTCACCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG CGGAATCCCAACGCAGGAACCAAAAAACACTCCCCCAAAAAAATGGCGCTAAGGCCGAGAGAAAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56116626..56116675 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 115882 RMVar_ID_115882 Human_SNP_ID_814057322 m1A Human chr12 - 118136200 118136200 118136200 CACTTGCTGAGGTCCACCGGCATGGCGAGGCCAAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTAG CACTTGCTGAGGTCCACCGGCATGGCGAGGCCGAGCAGAGCGTGCAGCCGGGAGTGCCGCGGTAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:118136101..118138075 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 115883 RMVar_ID_115883 Human_SNP_ID_814068829 m1A Human chr12 - 98516148 98516148 98516148 GCCCGCCTTTGTAGCCCCGGCCCCGCGTCCTTACCCTGCCGACGGCTGCTCGGCTCCGGCCCGCG GCCCGCCTTTGTAGCCCCGGCCCCGCGTCCTTCCCCTGCCGACGGCTGCTCGGCTCCGGCCCGCG T G TMPO-AS1 Ensembl:ENSG00000257167 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:98516001..98516200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4260901 115884 RMVar_ID_115884 Human_SNP_ID_814075971 m1A Human chr12 + 67269662 67269662 67269662 GGAGGAGCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG GGAGGAGCTCCAGTGGCGGCGGCGGCGGCGGCGGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAG A G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:67269566..67269775;chr12:67269380..67269779 26863196 MeRIP-seq:(Medium) rs1004927322 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 115885 RMVar_ID_115885 Human_SNP_ID_814099179 m1A Human chr12 + 106138553 106138553 106138553 GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCAGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG GCCGCTTCACCCCGTGCGGCTTCCTGGGCTCCCGGGCTGCAGTCGCCCCCGCCACCGCCTCTCGG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:106138506..106138638 26863196 MeRIP-seq:(Medium) rs751592845 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 115886 RMVar_ID_115886 Human_SNP_ID_814102083 m1A Human chr12 + 52897470 52897470 52897470 AGGACGTCAGAGGACTCAGACACCAGCTTCCCATCACGTGTCTCGATCTTCTTCACAACCACGGC AGGACGTCAGAGGACTCAGACACCAGCTTCCCCTCACGTGTCTCGATCTTCTTCACAACCACGGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52897301..52897599 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115887 RMVar_ID_115887 Human_SNP_ID_814102631 m1A Human chr12 - 56600297 56600297 56600297 GGCTGCCCTGGAACAGAATGTAGAACGGCGGTACCTGCGGGAGCCCCTCTGGCCAACTCATGAGG GGCTGCCCTGGAACAGAATGTAGAACGGCGGTGCCTGCGGGAGCCCCTCTGGCCAACTCATGAGG T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:56600246..56600686 32194978 MeRIP-seq:(Medium) rs200393909 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_229703,Human_RBP_ID_4257594,Human_RBP_ID_5461980,Human_RBP_ID_8783612,Human_RBP_ID_9255494,Human_RBP_ID_9278279,Human_RBP_ID_18975814 Human_Splice_Rec_1384899,Human_Splice_Rec_1384955,Human_Splice_Rec_1384979,Human_Splice_Rec_1385035 RMVar_hsa_circ_60919 115888 RMVar_ID_115888 Human_SNP_ID_814111274 m1A Human chr12 + 131916004 131916004 131916004 ACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCACGGACCCCCTGGGAGCTGTGTTCAGCCCACCA ACGTCGTCCGCCCCAAGCTGCCCAAACCCCCCCCGGACCCCCTGGGAGCTGTGTTCAGCCCACCA A C ULK1 Ensembl:ENSG00000177169 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c chr12:131915876..131916195;chr12:131915924..131916175 26863196 MeRIP-seq:(Medium) rs1176637341 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5491222,Human_RBP_ID_27806267 RMVar_hsa_circ_93798,RMVar_hsa_circ_161746,RMVar_hsa_circ_161747,RMVar_hsa_circ_82030,RMVar_hsa_circ_9023 115889 RMVar_ID_115889 Human_SNP_ID_814112300 m1A Human chr12 - 118052478 118052478 118052478 GTGTGTTTGAAGCATGTTGTCTCCTGCCCCAGAGGAACCGCTGCTGCTGGCCGAACTCAAGCCCG GTGTGTTTGAAGCATGTTGTCTCCTGCCCCAGGGGAACCGCTGCTGCTGGCCGAACTCAAGCCCG T C WSB2 Ensembl:ENSG00000176871 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:118052376..118052556 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_875213,Human_RBP_ID_4247875,Human_RBP_ID_22645430 Human_Splice_Rec_1430956,Human_Splice_Rec_1430968,Human_Splice_Rec_1430984,Human_Splice_Rec_1431000,Human_Splice_Rec_1431026,Human_Splice_Rec_1431046,Human_Splice_Rec_1431054,Human_Splice_Rec_1431064,Human_Splice_Rec_1431070 Human_miRNA_ID_2100973,Human_miRNA_ID_2106927,Human_miRNA_ID_2112870,Human_miRNA_ID_2165415,Human_miRNA_ID_2596662,Human_miRNA_ID_2739570,Human_miRNA_ID_2756719,Human_miRNA_ID_3040170 RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_22776,RMVar_hsa_circ_106798,RMVar_hsa_circ_160550 115890 RMVar_ID_115890 Human_SNP_ID_814114565 m1A Human chr12 - 52899839 52899839 52899839 GCACGGGGATGACCTGCGGCGCACAAAGACTGAGATCTCTGAGATGAACCGGAACATCAGCCGGC GCACGGGGATGACCTGCGGCGCACAAAGACTGGGATCTCTGAGATGAACCGGAACATCAGCCGGC T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52899789..52899985 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma 4 lung Human_RBP_ID_1473256,Human_RBP_ID_8378444,Human_RBP_ID_22437061,Human_RBP_ID_27422841 Human_Splice_Rec_1372619,Human_Splice_Rec_1372635,Human_Splice_Rec_1372645,Human_Splice_Rec_1372657,Human_Splice_Rec_1372673,Human_Splice_Rec_1372689,Human_Splice_Rec_1372701 Human_miRNA_ID_3002690 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_105363,RMVar_hsa_circ_107275,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_156776,RMVar_hsa_circ_96983,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_125884,RMVar_hsa_circ_156769,RMVar_hsa_circ_117415,RMVar_hsa_circ_156781,RMVar_hsa_circ_156782,RMVar_hsa_circ_156780 115891 RMVar_ID_115891 Human_SNP_ID_814119951 m1A Human chr12 - 9420275 9420275 9420275 GAGACCTGGCACCCTGAACCTGTCTCTGGGAAATGTCCTCTGTCTTTCTCAGATATTCCAGGAAC GAGACCTGGCACCCTGAACCTGTCTCTGGGAAGTGTCCTCTGTCTTTCTCAGATATTCCAGGAAC T C DDX12P Ensembl:ENSG00000214826 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10843741 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_1337689 RMVar_hsa_circ_115903,RMVar_hsa_circ_154844 115892 RMVar_ID_115892 Human_SNP_ID_814120318 m1A Human chr12 + 131799058 131799058 131799058 CTCTGCATTAGGGGAGTCTCTCAGGAAAAAGAAGCCCAGATCTCTTCAGCAATCGTTTCTTCCGT CTCTGCATTAGGGGAGTCTCTCAGGAAAAAGAGGCCCAGATCTCTTCAGCAATCGTTTCTTCCGT A G SFSWAP Ensembl:ENSG00000061936 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:131797199..131799076 32194978 MeRIP-seq:(Medium) rs780764619 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver Human_Splice_Rec_1445250,Human_Splice_Rec_1445251,Human_Splice_Rec_1445338,Human_Splice_Rec_1445339,Human_Splice_Rec_1445364,Human_Splice_Rec_1445365,Human_Splice_Rec_1445368,Human_Splice_Rec_1445369 115893 RMVar_ID_115893 Human_SNP_ID_814125338 m1A Human chr12 - 108530192 108530192 108530192 AAAAAAGAAGAAAAAGATCAGAGGCCCAGAGAAGCGCGGAGCAGATGAGGATGATGAGAAAGAGT AAAAAAGAAGAAAAAGATCAGAGGCCCAGAGAGGCGCGGAGCAGATGAGGATGATGAGAAAGAGT T C SART3 Ensembl:ENSG00000075856 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:108526526..108530325 26863196 MeRIP-seq:(Medium) rs776107033 Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_33368,Human_RBP_ID_228475,Human_RBP_ID_3942045,Human_RBP_ID_6126994,Human_RBP_ID_8229960,Human_RBP_ID_9365501,Human_RBP_ID_24543161,Human_RBP_ID_26321015,Human_RBP_ID_27807134 Human_Splice_Rec_1419495,Human_Splice_Rec_1419529,Human_Splice_Rec_1419565,Human_Splice_Rec_1419601,Human_Splice_Rec_1419635 RMVar_hsa_circ_44654,RMVar_hsa_circ_364089,RMVar_hsa_circ_364163,RMVar_hsa_circ_57993 115894 RMVar_ID_115894 Human_SNP_ID_814125676 m1A Human chr12 + 6581149 6581149 6581149 AGGGGGTTCAACAACGACCTTTTCATCCTCTGAGGCAGGGGCAGGGGCCTGTGTACACTTCAAAG AGGGGGTTCAACAACGACCTTTTCATCCTCTGGGGCAGGGGCAGGGGCCTGTGTACACTTCAAAG A G AC006064.2 Ensembl:ENSG00000247853 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6581101..6581175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 12 lung 115895 RMVar_ID_115895 Human_SNP_ID_814136302 m1A Human chr12 - 52949310 52949310 52949310 CGCCCCTGAAGCTGGTGGAGCGGGACACGGAGATCCGGGAACCAGAGCCCCCAGCGCCTGCATAG CGCCCCTGAAGCTGGTGGAGCGGGACACGGAGGTCCGGGAACCAGAGCCCCCAGCGCCTGCATAG T C KRT8 Ensembl:ENSG00000170421 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:52949126..52949417 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - RMVar_hsa_circ_98349,RMVar_hsa_circ_156769 115896 RMVar_ID_115896 Human_SNP_ID_814140695 m1A Human chr12 + 55757469 55757469 55757469 TTAGGCATATATGTGACCAAGAAGAAGGAGAGAAATGGAAAACACTGGAGAACAGAAAGTATCAG TTAGGCATATATGTGACCAAGAAGAAGGAGAGGAATGGAAAACACTGGAGAACAGAAAGTATCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55757291..55757492 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 115897 RMVar_ID_115897 Human_SNP_ID_814148174 m1A Human chr12 - 52901998 52901998 52901998 TGGAGCCTCCTGCAGCAGCAGAAGACGGCTCGAAGCAACATGGACAACATGTTCGAGAGCTACAT TGGAGCCTCCTGCAGCAGCAGAAGACGGCTCGGAGCAACATGGACAACATGTTCGAGAGCTACAT T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52901945..52902037 26863196 MeRIP-seq:(Medium) rs1555186665 Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_8378446,Human_RBP_ID_9344263,Human_RBP_ID_9364938,Human_RBP_ID_18469319,Human_RBP_ID_22437068,Human_RBP_ID_22493407,Human_RBP_ID_22756770 Human_Splice_Rec_1372612,Human_Splice_Rec_1372628,Human_Splice_Rec_1372642,Human_Splice_Rec_1372652,Human_Splice_Rec_1372666,Human_Splice_Rec_1372682,Human_Splice_Rec_1372714,Human_Splice_Rec_1372730,Human_Splice_Rec_1372738 RMVar_hsa_circ_98349,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769,RMVar_hsa_circ_109596,RMVar_hsa_circ_156783 115898 RMVar_ID_115898 Human_SNP_ID_814155273 m1A Human chr12 - 124356597 124356597 124356597 GCCCGAGCTTGGGCTTCTTCAGCCAGTGCACAATCGCTGTTTGCACTGTTTGCACTGGCTCAGAG GCCCGAGCTTGGGCTTCTTCAGCCAGTGCACAGTCGCTGTTTGCACTGTTTGCACTGGCTCAGAG T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124356595..124356843 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_24406673 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_50097,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_346115,RMVar_hsa_circ_104619,RMVar_hsa_circ_25865,RMVar_hsa_circ_161518 115899 RMVar_ID_115899 Human_SNP_ID_814178859 m1A Human chr12 + 131395765 131395765 131395765 TGGTGATGGTGATGGTGATGATGGTGATGATGATGATGGTGATGATGATGGTGATGGTGATGGTG TGGTGATGGTGATGGTGATGATGGTGATGATGGTGATGGTGATGATGATGGTGATGGTGATGGTG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:131395715..131395819 26863196 MeRIP-seq:(Medium) rs1029257918 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115900 RMVar_ID_115900 Human_SNP_ID_814180172 m1A Human chr12 + 6492939 6492939 6492939 CGTTCCAACGATCAACCACTTTGGGGGGCGGGAGAGTGAGCCTTATACCGATCAATCTAGGCACA CGTTCCAACGATCAACCACTTTGGGGGGCGGGTGAGTGAGCCTTATACCGATCAATCTAGGCACA A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6492272..6492958 32194978 MeRIP-seq:(Medium) rs746799618 Functional Loss SNV ICGC,COSMIC 33..33 33 BOCA,bone dedifferentiated,femur dedifferentiated 7 bone 115901 RMVar_ID_115901 Human_SNP_ID_814218699 m1A Human chr12 - 5921136 5921136 5921136 CATGCTGGGGGCCCAGGTGACATTGAGCTGGGACCGCTCGATGCCCTGGAGGAGGAGAGGAAGGA CATGCTGGGGGCCCAGGTGACATTGAGCTGGGGCCGCTCGATGCCCTGGAGGAGGAGAGGAAGGA T C ANO2 Ensembl:ENSG00000047617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5921087..5921177 26863196 MeRIP-seq:(Medium) rs3741902 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,COCA,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue,breast Human_Splice_Rec_1326927,Human_Splice_Rec_1326969,Human_Splice_Rec_1327019,Human_Splice_Rec_1327069 GWAS_ID_11832,GWAS_ID_11833,GWAS_ID_11834,GWAS_ID_11835,GWAS_ID_11836,GWAS_ID_11837,GWAS_ID_11838,GWAS_ID_11839,GWAS_ID_11840,GWAS_ID_11841,GWAS_ID_11842,GWAS_ID_11843,GWAS_ID_11844,GWAS_ID_11845,GWAS_ID_11846,GWAS_ID_11847,GWAS_ID_11848,GWAS_ID_11849,GWAS_ID_11850,GWAS_ID_11851,GWAS_ID_11852,GWAS_ID_11853,GWAS_ID_11854,GWAS_ID_11855,GWAS_ID_11856,GWAS_ID_11857 RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_126802,RMVar_hsa_circ_363675,RMVar_hsa_circ_320262,RMVar_hsa_circ_154431,RMVar_hsa_circ_78556,RMVar_hsa_circ_154430 115902 RMVar_ID_115902 Human_SNP_ID_814219188 m1A Human chr12 - 56645852 56645852 56645852 CCCCAGCTCAGCTCTTACTGCGGGCCGCTCCGACGGCGGTCCATCCTGGTAAGTGCTTTTCTCTA CCCCAGCTCAGCTCTTACTGCGGGCCGCTCCGGCGGCGGTCCATCCTGGTAAGTGCTTTTCTCTA T C ATP5F1B Ensembl:ENSG00000110955 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney Human_RBP_ID_424282,Human_RBP_ID_753236,Human_RBP_ID_1474663,Human_RBP_ID_4233652,Human_RBP_ID_8783759,Human_RBP_ID_9278307,Human_RBP_ID_9322577,Human_RBP_ID_18630053,Human_RBP_ID_19058460,Human_RBP_ID_22175956,Human_RBP_ID_22435994,Human_RBP_ID_27216736 Human_Splice_Rec_1385115,Human_Splice_Rec_1385135,Human_Splice_Rec_1385149,Human_Splice_Rec_1385163,Human_Splice_Rec_1385181,Human_Splice_Rec_1385191 RMVar_hsa_circ_112545,RMVar_hsa_circ_157439,RMVar_hsa_circ_77170,RMVar_hsa_circ_157440,RMVar_hsa_circ_80703,RMVar_hsa_circ_157448 115903 RMVar_ID_115903 Human_SNP_ID_814223644 m1A Human chr12 - 57696026 57696026 57696026 GAATCCCACACTCTTGCCACCTTGGCTGTTTCATCATCCCAGTCGAAGGCTGATTGGTAGTAGCC GAATCCCACACTCTTGCCACCTTGGCTGTTTCGTCATCCCAGTCGAAGGCTGATTGGTAGTAGCC T C AC025165.2 Ensembl:ENSG00000257342 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57695975..57696075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 115904 RMVar_ID_115904 Human_SNP_ID_814233144 m1A Human chr12 - 6916477 6916477 6916477 TGCCTAAGTAACGCTGTTTGTCTCCATCCCTCAGCTCCAGGGCCTCATAGATGCCCGTAGAGGCT TGCCTAAGTAACGCTGTTTGTCTCCATCCCTCCGCTCCAGGGCCTCATAGATGCCCGTAGAGGCT T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6915776..6916569 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine 115905 RMVar_ID_115905 Human_SNP_ID_814249970 m1A Human chr12 - 114683666 114683663 114683667 GACAGATAGGGGGCGGGGGAAGAAGAAAAAGAAAGGTAAAAAGTCTTCTAGGAGAACCTTTCACA GACAGATAGGGGGCGGGGGAAGAAGAAAAAG____GTAAAAAGTCTTCTAGGAGAACCTTTCACA CCTTT C TBX3 Ensembl:ENSG00000135111 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:114683616..114683752 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..35 33 PRAD 1 - Human_RBP_ID_4250284,Human_RBP_ID_24934511 115906 RMVar_ID_115906 Human_SNP_ID_814256748 m1A Human chr12 - 48135040 48135040 48135040 ATTCTAAGGCCTCTCTGGCTTCATTCATACGAACATTCTTGATGTCTTCTGAGGTGATTGGTTTT ATTCTAAGGCCTCTCTGGCTTCATTCATACGACCATTCTTGATGTCTTCTGAGGTGATTGGTTTT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48135026..48135050 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - 115907 RMVar_ID_115907 Human_SNP_ID_814257658 m1A Human chr12 - 8943902 8943902 8943902 TCCATTTTCCTTGTCCCTCCTCAGGTAATTGGATCATGCTGATCTATAAAGGGGGTGATGAATAT TCCATTTTCCTTGTCCCTCCTCAGGTAATTGGGTCATGCTGATCTATAAAGGGGGTGATGAATAT T C M6PR Ensembl:ENSG00000003056 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:8943851..8945281 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_429833,Human_RBP_ID_3941461,Human_RBP_ID_9023492,Human_RBP_ID_9364645,Human_RBP_ID_17830709,Human_RBP_ID_22644625,Human_RBP_ID_26321196 Human_Splice_Rec_1336986,Human_Splice_Rec_1337010,Human_Splice_Rec_1337028,Human_Splice_Rec_1337034,Human_Splice_Rec_1337042 RMVar_hsa_circ_272751,RMVar_hsa_circ_267541,RMVar_hsa_circ_154795 115908 RMVar_ID_115908 Human_SNP_ID_814258103 m1A Human chr12 - 95003631 95003631 95003631 CCTGAAACGCGGGCTGCAGCAGATCACCGGCCACGGCGGTCTCCGAGGCTATCTACGGGTTTTTT CCTGAAACGCGGGCTGCAGCAGATCACCGGCCTCGGCGGTCTCCGAGGCTATCTACGGGTTTTTT T A NDUFA12 Ensembl:ENSG00000184752 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:95002751..95003721 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_4244613,Human_RBP_ID_9023727,Human_RBP_ID_12060728,Human_RBP_ID_18634927,Human_RBP_ID_23208180 Human_Splice_Rec_1408223,Human_Splice_Rec_1408239,Human_Splice_Rec_1408245,Human_Splice_Rec_1408253,Human_Splice_Rec_1408259,Human_Splice_Rec_1408263 Human_miRNA_ID_2027357 RMVar_hsa_circ_111874,RMVar_hsa_circ_158822 115909 RMVar_ID_115909 Human_SNP_ID_814266095 m1A Human chr12 - 56327517 56327517 56327517 ATGGCAACCTGCTAGCTGCCTGTGGCTTCTCCAGCCGCCTCACTGGCCTGGCCTGCGACCGTTTC ATGGCAACCTGCTAGCTGCCTGTGGCTTCTCCTGCCGCCTCACTGGCCTGGCCTGCGACCGTTTC T A PAN2 Ensembl:ENSG00000135473 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56327466..56327558 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_5522077,Human_RBP_ID_9365069,Human_RBP_ID_18629809 RMVar_hsa_circ_90927,RMVar_hsa_circ_62764,RMVar_hsa_circ_157341,RMVar_hsa_circ_58428,RMVar_hsa_circ_64656 115910 RMVar_ID_115910 Human_SNP_ID_814269388 m1A Human chr12 - 125065545 125065545 125065545 GCGGGCGGCCGGGGCTGCGACGAGGGCTGGGGACCAGGGGCCGGGGCTGAGGCGAGGGCCGGGGA GCGGGCGGCCGGGGCTGCGACGAGGGCTGGGGGCCAGGGGCCGGGGCTGAGGCGAGGGCCGGGGA T C - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:125065453..125065551 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115911 RMVar_ID_115911 Human_SNP_ID_814273770 m1A Human chr12 - 108788273 108788273 108788273 CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACACAGGAGATTGAGACCCGGCTCCGGCTGGCGGG CGTGGGAAGCCCGGGCTGGTGAAGCAGCGGACGCAGGAGATTGAGACCCGGCTCCGGCTGGCGGG T C SSH1 Ensembl:ENSG00000084112 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3741778 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 head and neck,haematopoietic and lymphoid tissue 115912 RMVar_ID_115912 Human_SNP_ID_814274603 m1A Human chr12 - 5922711 5922711 5922711 CCAGGGCCCCAAACATGGACAGCAGTGTCTCAAGATGCCAGGTCCCCGGGCCCCAGGTCTGCAGG CCAGGGCCCCAAACATGGACAGCAGTGTCTCAGGATGCCAGGTCCCCGGGCCCCAGGTCTGCAGG T C ANO2 Ensembl:ENSG00000047617 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:5922660..5922751 26863196 MeRIP-seq:(Medium) rs779917319 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_Splice_Rec_1326924,Human_Splice_Rec_1326925,Human_Splice_Rec_1326966,Human_Splice_Rec_1326967,Human_Splice_Rec_1327016,Human_Splice_Rec_1327017,Human_Splice_Rec_1327066,Human_Splice_Rec_1327067 RMVar_hsa_circ_87189,RMVar_hsa_circ_66965,RMVar_hsa_circ_363425,RMVar_hsa_circ_154426,RMVar_hsa_circ_80454,RMVar_hsa_circ_30648,RMVar_hsa_circ_359149,RMVar_hsa_circ_154427,RMVar_hsa_circ_378165,RMVar_hsa_circ_126802,RMVar_hsa_circ_363675,RMVar_hsa_circ_320262,RMVar_hsa_circ_154431,RMVar_hsa_circ_78556,RMVar_hsa_circ_154430 115913 RMVar_ID_115913 Human_SNP_ID_814275230 m1A Human chr12 - 104537852 104537852 104537852 ATCTCTACCAAGAAGTAAAAAGTTAGCCGGGCATGGTGGTACGCACCTGTGGTCCCGGTCATTCA ATCTCTACCAAGAAGTAAAAAGTTAGCCGGGCGTGGTGGTACGCACCTGTGGTCCCGGTCATTCA T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:104537826..104537939 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115914 RMVar_ID_115914 Human_SNP_ID_814297132 m1A Human chr12 + 69258759 69258759 69258759 CTTTTTCCTGGACAACCTTTTGGGCAGCCTCCATTGGGTCCACTTCCTCCTGGCCCTCCACCTCC CTTTTTCCTGGACAACCTTTTGGGCAGCCTCCGTTGGGTCCACTTCCTCCTGGCCCTCCACCTCC A G CPSF6 Ensembl:ENSG00000111605 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr12:69258659..69258959 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung Human_RBP_ID_426832,Human_RBP_ID_878591,Human_RBP_ID_1476727,Human_RBP_ID_3941982,Human_RBP_ID_4259399,Human_RBP_ID_8382705,Human_RBP_ID_12020007,Human_RBP_ID_17074919,Human_RBP_ID_17240379,Human_RBP_ID_17355902,Human_RBP_ID_17473363,Human_RBP_ID_17685242,Human_RBP_ID_18434718,Human_RBP_ID_18632584,Human_RBP_ID_19804379,Human_RBP_ID_22039446,Human_RBP_ID_22177154,Human_RBP_ID_22795228,Human_RBP_ID_24467579,Human_RBP_ID_26911177,Human_RBP_ID_27218072 Human_miRNA_ID_3078059,Human_miRNA_ID_3078060 RMVar_hsa_circ_158146,RMVar_hsa_circ_277579,RMVar_hsa_circ_286191,RMVar_hsa_circ_105735,RMVar_hsa_circ_158148,RMVar_hsa_circ_158147,RMVar_hsa_circ_158145,RMVar_hsa_circ_158150,RMVar_hsa_circ_334555,RMVar_hsa_circ_353172,RMVar_hsa_circ_313813,RMVar_hsa_circ_333036,RMVar_hsa_circ_271894,RMVar_hsa_circ_158151,RMVar_hsa_circ_306002 115915 RMVar_ID_115915 Human_SNP_ID_814298591 m1A Human chr12 + 67269668 67269668 67269668 GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCAGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG GCTCCAGTGGCGGCGGCGGCGGCGGCAGCGGCGGCGGGCAGCAGCTCCAGCAGCGCCAGCAGGCG A G CAND1 Ensembl:ENSG00000111530 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:67269380..67269750;chr12:67269384..67269775;chr12:67269549..67269722 26863196 MeRIP-seq:(Medium) rs746228572 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_229826,Human_RBP_ID_754643,Human_RBP_ID_4246840,Human_RBP_ID_9279131,Human_RBP_ID_22437304 115916 RMVar_ID_115916 Human_SNP_ID_814301612 m1A Human chr12 - 56640115 56640115 56640115 ACTACGTTTGCCCATTTGGATGCTACCACTGTACTGTCGCGTGCCATTGCTGAGCTGGGCATCTA ACTACGTTTGCCCATTTGGATGCTACCACTGTGCTGTCGCGTGCCATTGCTGAGCTGGGCATCTA T C ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56640066..56640249 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_RBP_ID_33820,Human_RBP_ID_424231,Human_RBP_ID_877206,Human_RBP_ID_1081968,Human_RBP_ID_1167643,Human_RBP_ID_1474609,Human_RBP_ID_1797896,Human_RBP_ID_3409525,Human_RBP_ID_4233592,Human_RBP_ID_6201515,Human_RBP_ID_8247750,Human_RBP_ID_8380171,Human_RBP_ID_8783711,Human_RBP_ID_9018765,Human_RBP_ID_11989634,Human_RBP_ID_17239736,Human_RBP_ID_19703627,Human_RBP_ID_22435990,Human_RBP_ID_22532498,Human_RBP_ID_22756816,Human_RBP_ID_22794793,Human_RBP_ID_23567209,Human_RBP_ID_26909472,Human_RBP_ID_27154917,Human_RBP_ID_27216710,Human_RBP_ID_27423707,Human_RBP_ID_27558150 Human_Splice_Rec_1385128,Human_Splice_Rec_1385146,Human_Splice_Rec_1385162,Human_Splice_Rec_1385174,Human_Splice_Rec_1385180,Human_Splice_Rec_1385190 Human_miRNA_ID_1935278,Human_miRNA_ID_2134242 RMVar_hsa_circ_85227,RMVar_hsa_circ_118862,RMVar_hsa_circ_127607,RMVar_hsa_circ_95555,RMVar_hsa_circ_109546,RMVar_hsa_circ_74767,RMVar_hsa_circ_157428,RMVar_hsa_circ_157430,RMVar_hsa_circ_157432,RMVar_hsa_circ_77423,RMVar_hsa_circ_157433,RMVar_hsa_circ_157431,RMVar_hsa_circ_157429,RMVar_hsa_circ_123639,RMVar_hsa_circ_315651,RMVar_hsa_circ_87740,RMVar_hsa_circ_112545,RMVar_hsa_circ_157434,RMVar_hsa_circ_157435,RMVar_hsa_circ_373395,RMVar_hsa_circ_302934,RMVar_hsa_circ_108564,RMVar_hsa_circ_157437,RMVar_hsa_circ_157438,RMVar_hsa_circ_157439,RMVar_hsa_circ_157436 115917 RMVar_ID_115917 Human_SNP_ID_814306844 m1A Human chr12 + 85280278 85280278 85280278 ACAGTCTTCCAGGATTATGGAGTTTCTGAGCGAGAAGTTTGCCCTCAAGAGCCCTCCGAGTAAAA ACAGTCTTCCAGGATTATGGAGTTTCTGAGCGGGAAGTTTGCCCTCAAGAGCCCTCCGAGTAAAA A G ALX1 Ensembl:ENSG00000180318 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:85280234..85280319 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 2 stomach Human_RBP_ID_8384811 115918 RMVar_ID_115918 Human_SNP_ID_814314648 m1A Human chr12 - 71663742 71663742 71663742 TGGGGTGCTGGGGTGCGGGGAAGTTGGGGAGCAGAGGCCGCTTGGTGTCCGAGTAGGGTAAGACC TGGGGTGCTGGGGTGCGGGGAAGTTGGGGAGCGGAGGCCGCTTGGTGTCCGAGTAGGGTAAGACC T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:71663651..71663850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_3943321,Human_RBP_ID_5139906,Human_RBP_ID_5521664,Human_RBP_ID_8229919,Human_RBP_ID_9415906,Human_RBP_ID_17067249,Human_RBP_ID_18417301,Human_RBP_ID_22710087,Human_RBP_ID_22910568,Human_RBP_ID_23113380,Human_RBP_ID_25027351,Human_RBP_ID_26321730,Human_RBP_ID_27805684 115919 RMVar_ID_115919 Human_SNP_ID_814323285 m1A Human chr12 - 120130738 120130738 120130738 CTGTCTGTTCTCCACAGATCCCCATTGCGGTGAGCGGGGTCCGGGGCATGGGCTTTCTCATGAGA CTGTCTGTTCTCCACAGATCCCCATTGCGGTGGGCGGGGTCCGGGGCATGGGCTTTCTCATGAGA T C GCN1 Ensembl:ENSG00000089154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120130688..120130788 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_33573,Human_RBP_ID_753063,Human_RBP_ID_5521787,Human_RBP_ID_6246018,Human_RBP_ID_8229983,Human_RBP_ID_8787393,Human_RBP_ID_9279272,Human_RBP_ID_18160580,Human_RBP_ID_22573591,Human_RBP_ID_24530222 Human_Splice_Rec_1432378,Human_Splice_Rec_1432379 RMVar_hsa_circ_160653,RMVar_hsa_circ_111513,RMVar_hsa_circ_121944,RMVar_hsa_circ_101268,RMVar_hsa_circ_160654,RMVar_hsa_circ_110069,RMVar_hsa_circ_160652,RMVar_hsa_circ_160655 115920 RMVar_ID_115920 Human_SNP_ID_814326742 m1A Human chr12 + 2859174 2859174 2859174 TCCTCCCACTTCCTGGGAGTAGCTGAGCTGGGAGGCAGGGTCAGAGGAGTCTGCTGGGAACGGGA TCCTCCCACTTCCTGGGAGTAGCTGAGCTGGGTGGCAGGGTCAGAGGAGTCTGCTGGGAACGGGA A T ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2859126..2859225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 115921 RMVar_ID_115921 Human_SNP_ID_814340749 m1A Human chr12 - 52172276 52172276 52172276 GCAGGACATGGCGCGGCAGCTGCGCAAGTACCAGGAGCTGATGAACGTCAAGCTGGCCCTGGACA GCAGGACATGGCGCGGCAGCTGCGCAAGTACCGGGAGCTGATGAACGTCAAGCTGGCCCTGGACA T C KRT80 Ensembl:ENSG00000167767 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:52172228..52172379 32194978 MeRIP-seq:(Medium) rs1296933681 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_Splice_Rec_1371659,Human_Splice_Rec_1371675,Human_Splice_Rec_1371687 RMVar_hsa_circ_120230,RMVar_hsa_circ_156658 115922 RMVar_ID_115922 Human_SNP_ID_814349008 m1A Human chr12 + 53973612 53973612 53973612 CCTCATGAAAAACGAAGGCTCCTACGGCGGCCACCACCACCCCAGCGCCCCGCACGCAACCCCCG CCTCATGAAAAACGAAGGCTCCTACGGCGGCCCCCACCACCCCAGCGCCCCGCACGCAACCCCCG A C HOXC11 Ensembl:ENSG00000123388 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53973252..53973672 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_miRNA_ID_2684930,Human_miRNA_ID_3065953 RMVar_hsa_circ_110245,RMVar_hsa_circ_157008 115923 RMVar_ID_115923 Human_SNP_ID_814361762 m1A Human chr12 + 51238919 51238919 51238919 CAAACCGGACCCGCAACCACCATGAACAGCAAAGGCAAGGACCGAGGGTGGCAGAGGCCGTCGGG CAAACCGGACCCGCAACCACCATGAACAGCAAGGGCAAGGACCGAGGGTGGCAGAGGCCGTCGGG A G DAZAP2 Ensembl:ENSG00000183283 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:51238826..51238978;chr12:51238851..51238950 26863410 MeRIP-seq:(Medium) rs1451550764 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 8 oesophagus Human_RBP_ID_4246662,Human_RBP_ID_17357015,Human_RBP_ID_19056172,Human_RBP_ID_26416974 Human_Splice_Rec_1369909,Human_Splice_Rec_1369917 RMVar_hsa_circ_156588,RMVar_hsa_circ_77809 115924 RMVar_ID_115924 Human_SNP_ID_814362314 m1A Human chr12 + 6200436 6200436 6200436 GCCTGCATCTGTATCCAGCGCCAGGTCCCGCCAGTCCCAGCTGCGCGCGCCCCCCAGTCCCGCAC GCCTGCATCTGTATCCAGCGCCAGGTCCCGCCGGTCCCAGCTGCGCGCGCCCCCCAGTCCCGCAC A G CD9 Ensembl:ENSG00000010278 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6200357..6200575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_36251,Human_RBP_ID_229630,Human_RBP_ID_809980,Human_RBP_ID_4236085 Human_Splice_Rec_1327318,Human_Splice_Rec_1327352 115925 RMVar_ID_115925 Human_SNP_ID_814369908 m1A Human chr12 - 48818877 48818877 48818877 AGCGAGCGGCGCCGGGGGCGGGAGCGGCCCGGAGGCAGGGGCAAGGACTGCGGGCCGCGCCCGGG AGCGAGCGGCGCCGGGGGCGGGAGCGGCCCGGGGGCAGGGGCAAGGACTGCGGGCCGCGCCCGGG T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48818826..48819637 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 115926 RMVar_ID_115926 Human_SNP_ID_814381678 m1A Human chr12 + 13000111 13000111 13000111 GCTTCCGAACAGCGAGTTCTTGATCATGCCCAACATGTTGTAGCCGAGACGCTCCCGACGCACGG GCTTCCGAACAGCGAGTTCTTGATCATGCCCAGCATGTTGTAGCCGAGACGCTCCCGACGCACGG A G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:12999979..13000283 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115927 RMVar_ID_115927 Human_SNP_ID_814387455 m1A Human chr12 - 63779945 63779945 63779945 TTCCGCGTCAGCCGCATCCCACTCGGGCTTCCAGTCAGGCATCCACCGCCATGGAGCGGGCGGAA TTCCGCGTCAGCCGCATCCCACTCGGGCTTCCGGTCAGGCATCCACCGCCATGGAGCGGGCGGAA T C AC084357.2 Ensembl:ENSG00000249753 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:63779894..63780083 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,gastroesophageal_junction adenocarcinoma 1 stomach 115928 RMVar_ID_115928 Human_SNP_ID_814387668 m1A Human chr12 + 56164274 56164274 56164274 TCACCCTCCCTCCAGGTGGACCCCTCTCCCTCACCCTTCTCCCCTCTTGGCCCCTTCTCACCTGG TCACCCTCCCTCCAGGTGGACCCCTCTCCCTCTCCCTTCTCCCCTCTTGGCCCCTTCTCACCTGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56164271..56164757 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 115929 RMVar_ID_115929 Human_SNP_ID_814393586 m1A Human chr12 + 56160261 56160261 56160261 CTTTCCCCCTGCAGGTGAGAAGATGACAGAGGAAGAAGTAGAGATGCTGGTGGCAGGGCATGAGG CTTTCCCCCTGCAGGTGAGAAGATGACAGAGGGAGAAGTAGAGATGCTGGTGGCAGGGCATGAGG A G MYL6 Ensembl:ENSG00000092841 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56159945..56160372 26863196 MeRIP-seq:(Medium) rs981911509 Functional Loss SNV TCGA 33..33 33 UCS 1 - Human_RBP_ID_423676,Human_RBP_ID_811764,Human_RBP_ID_874684,Human_RBP_ID_1474274,Human_RBP_ID_1797571,Human_RBP_ID_4231970,Human_RBP_ID_5111489,Human_RBP_ID_5139876,Human_RBP_ID_5346699,Human_RBP_ID_8379819,Human_RBP_ID_11985850,Human_RBP_ID_17649998,Human_RBP_ID_18977304,Human_RBP_ID_19703584,Human_RBP_ID_22040610,Human_RBP_ID_22435965,Human_RBP_ID_22574677,Human_RBP_ID_22755995,Human_RBP_ID_22905991,Human_RBP_ID_23113332,Human_RBP_ID_23207697,Human_RBP_ID_23566578,Human_RBP_ID_26322946,Human_RBP_ID_26418014,Human_RBP_ID_27423520,Human_RBP_ID_27805510 Human_Splice_Rec_1381754,Human_Splice_Rec_1381755,Human_Splice_Rec_1381762,Human_Splice_Rec_1381763,Human_Splice_Rec_1381774,Human_Splice_Rec_1381782,Human_Splice_Rec_1381783,Human_Splice_Rec_1381792,Human_Splice_Rec_1381793,Human_Splice_Rec_1381804,Human_Splice_Rec_1381805,Human_Splice_Rec_1381812,Human_Splice_Rec_1381816,Human_Splice_Rec_1381817,Human_Splice_Rec_1381826,Human_Splice_Rec_1381827,Human_Splice_Rec_1381836,Human_Splice_Rec_1381844,Human_Splice_Rec_1381845,Human_Splice_Rec_1381860,Human_Splice_Rec_1381861,Human_Splice_Rec_1381872,Human_Splice_Rec_1381890,Human_Splice_Rec_1381898,Human_Splice_Rec_1381899,Human_Splice_Rec_1381910,Human_Splice_Rec_1381911,Human_Splice_Rec_1381914,Human_Splice_Rec_1381915 Human_miRNA_ID_2441626 RMVar_hsa_circ_84206,RMVar_hsa_circ_81881,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_325389,RMVar_hsa_circ_36110,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235,RMVar_hsa_circ_126953,RMVar_hsa_circ_98857,RMVar_hsa_circ_157236,RMVar_hsa_circ_157237 115930 RMVar_ID_115930 Human_SNP_ID_814397906 m1A Human chr12 + 56163746 56163733 56163746 ACCGTGCCTGGGCTCGGGGCTGTGGGGTCTGGAGGCAGGGGGGTGCCTGGGTCTGTGGAGAAAAG ACCGTGCCTGGGCTCGGGGC_____________GGCAGGGGGGTGCCTGGGTCTGTGGAGAAAAG CTGTGGGGTCTGGA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56163564..56163791 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 21..33 33 LUAD 1 - 115931 RMVar_ID_115931 Human_SNP_ID_814402739 m1A Human chr12 - 67305680 67305680 67305680 TATAGTTTTTTATTAGAATATCAAGGGCAGAAAGAGTACCCAGTTTCAAAGCTCTCTGGTTTTTT TATAGTTTTTTATTAGAATATCAAGGGCAGAATGAGTACCCAGTTTCAAAGCTCTCTGGTTTTTT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:67305629..67305730 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 115932 RMVar_ID_115932 Human_SNP_ID_814409187 m1A Human chr12 + 122022020 122022020 122022020 GTGCGCGAGTGAGTGAGCGGCGGGCGGGCGCGAGTGTGGCCGCCGCGGAGCGCGAGCAGGACCCG GTGCGCGAGTGAGTGAGCGGCGGGCGGGCGCGGGTGTGGCCGCCGCGGAGCGCGAGCAGGACCCG A G BCL7A Ensembl:ENSG00000110987 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:122021907..122022058 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_872705,Human_RBP_ID_4251319,Human_RBP_ID_5139735,Human_RBP_ID_5283831,Human_RBP_ID_5315091,Human_RBP_ID_5644699,Human_RBP_ID_17242165,Human_RBP_ID_18417354,Human_RBP_ID_23113299,Human_RBP_ID_23543356 115933 RMVar_ID_115933 Human_SNP_ID_814414508 m1A Human chr12 - 100157705 100157705 100157705 GGCATTTTTCAACTCAGCTGTAGCTAGTGCCGAGGAGGAGCAGGCACGGCTATGTGGGCAGCTGA GGCATTTTTCAACTCAGCTGTAGCTAGTGCCGGGGAGGAGCAGGCACGGCTATGTGGGCAGCTGA T C GOLGA2P5 Ensembl:ENSG00000238105 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:100157486..100157766;chr12:100157656..100157746 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_874951,Human_RBP_ID_5521677,Human_RBP_ID_5556171 Human_Splice_Rec_1412610,Human_Splice_Rec_1412628,Human_Splice_Rec_1412634,Human_Splice_Rec_1412642,Human_Splice_Rec_1412668 115934 RMVar_ID_115934 Human_SNP_ID_814422087 m1A Human chr12 - 49128795 49128795 49128795 AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCAGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC AAGAAGTCCAAGCTGGAGTTCTCCATTTACCCGGCACCCCAGGTTTCCACAGCTGTAGTTGAGCC T C TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK-293T cells,m1A-quant-seq;HTR8/Svneo,Normoxia chr12:49128724..49129015 31548705,32194978 m1A-quant-seq:(High) rs1057725 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma,large_intestine adenocarcinoma 17 head and neck,large intestine Human_RBP_ID_420813,Human_RBP_ID_753565,Human_RBP_ID_878225,Human_RBP_ID_992560,Human_RBP_ID_1235996,Human_RBP_ID_1269398,Human_RBP_ID_1357654,Human_RBP_ID_1472606,Human_RBP_ID_1796026,Human_RBP_ID_3406908,Human_RBP_ID_4255543,Human_RBP_ID_5140265,Human_RBP_ID_6190547,Human_RBP_ID_8377113,Human_RBP_ID_11954544,Human_RBP_ID_17238736,Human_RBP_ID_17354536,Human_RBP_ID_17471580,Human_RBP_ID_17820454,Human_RBP_ID_18188768,Human_RBP_ID_18627625,Human_RBP_ID_22435827,Human_RBP_ID_22532421,Human_RBP_ID_22794225,Human_RBP_ID_23561779,Human_RBP_ID_26907086,Human_RBP_ID_27214911,Human_RBP_ID_27629902 Human_miRNA_ID_2723904 Clinvar_Rec_449,Clinvar_Rec_450 GWAS_ID_10157,GWAS_ID_10158,GWAS_ID_10159,GWAS_ID_10160,GWAS_ID_10161,GWAS_ID_10162,GWAS_ID_10163,GWAS_ID_10164,GWAS_ID_10165,GWAS_ID_10166,GWAS_ID_10167,GWAS_ID_10168,GWAS_ID_10169,GWAS_ID_10170,GWAS_ID_10171,GWAS_ID_10172,GWAS_ID_10173,GWAS_ID_10174,GWAS_ID_10175,GWAS_ID_10176,GWAS_ID_10177,GWAS_ID_10178,GWAS_ID_10179,GWAS_ID_10180,GWAS_ID_10181,GWAS_ID_10182,GWAS_ID_10183,GWAS_ID_10184,GWAS_ID_10185,GWAS_ID_10186,GWAS_ID_10187,GWAS_ID_10188,GWAS_ID_10189,GWAS_ID_10190,GWAS_ID_10191,GWAS_ID_10192,GWAS_ID_10193,GWAS_ID_10194,GWAS_ID_10195,GWAS_ID_10196,GWAS_ID_10197,GWAS_ID_10198,GWAS_ID_10199,GWAS_ID_10200 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 115935 RMVar_ID_115935 Human_SNP_ID_814425125 m1A Human chr12 - 69586284 69586284 69586284 TCAGCTCCTGCCTTAAAGATGTTAACAGGTGCAAGGGAAAGGGACGCCTGAAAAGGAAAACCAAG TCAGCTCCTGCCTTAAAGATGTTAACAGGTGCGAGGGAAAGGGACGCCTGAAAAGGAAAACCAAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69586280..69586838 32194978 MeRIP-seq:(Medium) rs1320497230 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus 115936 RMVar_ID_115936 Human_SNP_ID_814429198 m1A Human chr12 - 56138222 56138222 56138222 AGTGGGACGGGGGGTGAGACGCTCCAGGCGCAAGTGCAGGCGGCCAGATGGGACATCCTCCAGGG AGTGGGACGGGGGGTGAGACGCTCCAGGCGCATGTGCAGGCGGCCAGATGGGACATCCTCCAGGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56138201..56138225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary 115937 RMVar_ID_115937 Human_SNP_ID_814460265 m1A Human chr12 + 6752039 6752039 6752039 CCTGACAACATACGGCTCATATGCTGACGGTGAATAGCAAAGGGATCCCTGTGGAGTGAGCACAT CCTGACAACATACGGCTCATATGCTGACGGTGGATAGCAAAGGGATCCCTGTGGAGTGAGCACAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6751879..6752097 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver 115938 RMVar_ID_115938 Human_SNP_ID_814469603 m1A Human chr12 - 121779064 121779064 121779064 CCTCCCTGGGCTCCCGAGATAGGCACCACTGTATCCTCCAGCTCCTTCCTTCCTTCCCCCAGGAA CCTCCCTGGGCTCCCGAGATAGGCACCACTGTCTCCTCCAGCTCCTTCCTTCCTTCCCCCAGGAA T G RHOF Ensembl:ENSG00000139725 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121779013..121779573 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_18935759,Human_RBP_ID_26413092,Human_RBP_ID_27425880 115939 RMVar_ID_115939 Human_SNP_ID_814473773 m1A Human chr12 + 124810242 124810242 124810242 TCAGGAGTCATGAAGGGCGGCCACATTTGCCCAGAAGTTCCATTGATCATGTTGCACTGATCGGA TCAGGAGTCATGAAGGGCGGCCACATTTGCCCGGAAGTTCCATTGATCATGTTGCACTGATCGGA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124810129..124810246 26863196 MeRIP-seq:(Medium) rs771694795 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 6 liver 115940 RMVar_ID_115940 Human_SNP_ID_814478951 m1A Human chr12 - 56165320 56165320 56165320 AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCATGGTAAGTGTTATGTTCCAGAACTTTTGTTGG AGTCCCACCAGGGGTTCCCCCCCCTGGACCCCTTGGTAAGTGTTATGTTCCAGAACTTTTGTTGG T A AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56165316..56165394 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_19058365 Human_Splice_Rec_1381975,Human_Splice_Rec_1382031,Human_Splice_Rec_1382089,Human_Splice_Rec_1382145,Human_Splice_Rec_1382199 RMVar_hsa_circ_35361,RMVar_hsa_circ_45211 115941 RMVar_ID_115941 Human_SNP_ID_814487266 m1A Human chr12 - 47702811 47702811 47702811 ATAATGACTTCAGCAAATAAAGCAATCGAATTACAACTACAAGTGAAACAAAATGCAGAAGAATT ATAATGACTTCAGCAAATAAAGCAATCGAATTGCAACTACAAGTGAAACAAAATGCAGAAGAATT T C RPAP3 Ensembl:ENSG00000005175 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:47702761..47702850 26863196 MeRIP-seq:(Medium) rs1316015105 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_4246601,Human_RBP_ID_26906495,Human_RBP_ID_27805416 Human_Splice_Rec_1359254,Human_Splice_Rec_1359318,Human_Splice_Rec_1359354 RMVar_hsa_circ_350857,RMVar_hsa_circ_61937 115942 RMVar_ID_115942 Human_SNP_ID_814498703 m1A Human chr12 - 6566135 6566135 6566135 CGATGCTGATACGGTAGATGACTATGGAGCTGACTCCAACTCTGAGGATGAGGAGGAAGGTGAAG CGATGCTGATACGGTAGATGACTATGGAGCTGCCTCCAACTCTGAGGATGAGGAGGAAGGTGAAG T G NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6566101..6566200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 10 brain Human_RBP_ID_994014,Human_RBP_ID_1799341,Human_RBP_ID_2349706,Human_RBP_ID_6210315,Human_RBP_ID_8784481,Human_RBP_ID_12010285,Human_RBP_ID_18976713,Human_RBP_ID_22910704 Human_Splice_Rec_1328935,Human_Splice_Rec_1328963,Human_Splice_Rec_1328993,Human_Splice_Rec_1329023,Human_Splice_Rec_1329053,Human_Splice_Rec_1329081,Human_Splice_Rec_1329109,Human_Splice_Rec_1329151,Human_Splice_Rec_1329191,Human_Splice_Rec_1329209,Human_Splice_Rec_1329223,Human_Splice_Rec_1329231,Human_Splice_Rec_1329343,Human_Splice_Rec_1329367 RMVar_hsa_circ_63050,RMVar_hsa_circ_38844 115943 RMVar_ID_115943 Human_SNP_ID_814531205 m1A Human chr12 - 124912958 124912958 124912958 AGGAAGGCATTCCTCCTGACCAGCAGAGGTTGATCTTTGCCGGAAAGCAGCTGGAAGATGGGCGC AGGAAGGCATTCCTCCTGACCAGCAGAGGTTGTTCTTTGCCGGAAAGCAGCTGGAAGATGGGCGC T A UBC Ensembl:ENSG00000150991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1790259,Human_RBP_ID_5554885,Human_RBP_ID_26903494 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161585 115944 RMVar_ID_115944 Human_SNP_ID_814542163 m1A Human chr12 - 12717450 12717450 12717450 GTCGCAGAGCCGTGAGCAAGCGGGGACAGGGGAGGGGGAGAAAAACACCCCGAAAAGACGAGCCC GTCGCAGAGCCGTGAGCAAGCGGGGACAGGGGGGGGGGAGAAAAACACCCCGAAAAGACGAGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:12717402..12717568 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 115945 RMVar_ID_115945 Human_SNP_ID_814557374 m1A Human chr12 - 120534786 120534786 120534786 GCGGCATCAACGGGGGCCTCGGCGGCGACGGCAGTCGGAGCGGAGCGGGCGCGGCGGGGACCCAG GCGGCATCAACGGGGGCCTCGGCGGCGACGGCGGTCGGAGCGGAGCGGGCGCGGCGGGGACCCAG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment chr12:120534376..120534975;chr12:120534737..120534828 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 115946 RMVar_ID_115946 Human_SNP_ID_814568199 m1A Human chr12 - 8082354 8082341 8082355 TACCTGTAACCGCGGTTGGAGGCCCGGGGCGGAATCCGGTAGACGCTGACGTCTGGCTTCACACA TACCTGTAACCGCGGTTGGAGGCCCGGGGCG______________CTGACGTCTGGCTTCACACA GCGTCTACCGGATTC G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr12:8082308..8082410;chr12:8082311..8082388 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..45 33 BRCA 1 - 115947 RMVar_ID_115947 Human_SNP_ID_814574375 m1A Human chr12 - 120496471 120496470 120496472 CCTGAGTAGCGCACTCCACCGAGTCCTGTTGCATCTCTTCCGACATGTCCGCATTTTTGATCACG CCTGAGTAGCGCACTCCACCGAGTCCTGTTG__TCTCTTCCGACATGTCCGCATTTTTGATCACG ATG A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120496358..120496476 26863196 MeRIP-seq:(Medium) rs1393054729 Functional Loss DEL ICGC 32..33 33 PBCA 1 - 115948 RMVar_ID_115948 Human_SNP_ID_814575493 m1A Human chr12 + 2858921 2858921 2858921 GTTCTGAACTGAGGAGCCTTTGCGGTGATTCAAGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG GTTCTGAACTGAGGAGCCTTTGCGGTGATTCAGGGGGGGGAGCACTTTGCAAGGGAGTGGTGCTG A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr12:2858901..2858925;chr12:2858876..2858975;chr12:2858872..2859052 26863196 MeRIP-seq:(Medium) rs563190488 Functional Loss SNV ICGC,COSMIC 33..33 33 BOCA,bone dedifferentiated,femur dedifferentiated 5 bone 115949 RMVar_ID_115949 Human_SNP_ID_814578157 m1A Human chr12 - 12718104 12718104 12718104 GCAGGCACCTTTGGGGGGCCGCGGGGGTCTGTAGTAGAACTCGGGCAAGCTGCCCTTCTCCACCT GCAGGCACCTTTGGGGGGCCGCGGGGGTCTGTGGTAGAACTCGGGCAAGCTGCCCTTCTCCACCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:12718054..12718202 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 115950 RMVar_ID_115950 Human_SNP_ID_814588300 m1A Human chr12 - 53295602 53295602 53295602 CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCC CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCCGATTCAGCTCCGTGATGTTAATAGACTGCGCC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53295526..53295679;chr12:53295551..53295625 26863196 MeRIP-seq:(Medium) rs199718276 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma,OV,oesophagus adenocarcinoma,ovary serous_carcinoma 18 ovary,oesophagus,stomach 115951 RMVar_ID_115951 Human_SNP_ID_814588301 m1A Human chr12 - 53295602 53295602 53295602 CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATAGACTGCGCC CCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCTGATTCAGCTCCGTGATGTTAATAGACTGCGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:53295526..53295679;chr12:53295551..53295625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 7 liver 115952 RMVar_ID_115952 Human_SNP_ID_814604869 m1A Human chr12 - 31089465 31089465 31089465 TGGCTACCGTGCCTGCTTCTCTGCATGTCCACACAGCGGTCGTTGATAAGCTGCACAGAACCTAG TGGCTACCGTGCCTGCTTCTCTGCATGTCCACGCAGCGGTCGTTGATAAGCTGCACAGAACCTAG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:31089459..31089610 26863196 MeRIP-seq:(Medium) rs3881298 Functional Loss SNV ICGC,COSMIC 33..33 33 bile_duct adenocarcinoma,thyroid neoplasm,biliary_tract adenocarcinoma,COCA 13 biliary tract,gallbladder,head and neck GWAS_ID_13237,GWAS_ID_13238,GWAS_ID_13239,GWAS_ID_13240,GWAS_ID_13241 115953 RMVar_ID_115953 Human_SNP_ID_814610957 m1A Human chr12 - 124483675 124483675 124483675 GGAGTTCATTGAAAGCAAGCGCCCTCGGCTAGAGCTGCTGCCTGACCCCCTGCTGCGACCGTCAC GGAGTTCATTGAAAGCAAGCGCCCTCGGCTAGCGCTGCTGCCTGACCCCCTGCTGCGACCGTCAC T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr12:124483626..124483775;chr12:124473112..124486376 26863196,26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_3942421,Human_RBP_ID_5554878,Human_RBP_ID_8778104,Human_RBP_ID_18188995 Human_Splice_Rec_1441294,Human_Splice_Rec_1441295,Human_Splice_Rec_1441388,Human_Splice_Rec_1441389,Human_Splice_Rec_1441618,Human_Splice_Rec_1441619,Human_Splice_Rec_1441762,Human_Splice_Rec_1441763,Human_Splice_Rec_1441838,Human_Splice_Rec_1441839,Human_Splice_Rec_1441861,Human_Splice_Rec_1441873 Human_miRNA_ID_1968685 RMVar_hsa_circ_55111,RMVar_hsa_circ_21997,RMVar_hsa_circ_376528,RMVar_hsa_circ_351509,RMVar_hsa_circ_67300,RMVar_hsa_circ_161535,RMVar_hsa_circ_378574,RMVar_hsa_circ_161537,RMVar_hsa_circ_270683,RMVar_hsa_circ_161545,RMVar_hsa_circ_161544,RMVar_hsa_circ_328847,RMVar_hsa_circ_301571,RMVar_hsa_circ_161543,RMVar_hsa_circ_72549,RMVar_hsa_circ_343277,RMVar_hsa_circ_62283,RMVar_hsa_circ_161546,RMVar_hsa_circ_290700,RMVar_hsa_circ_379002,RMVar_hsa_circ_284110,RMVar_hsa_circ_324824,RMVar_hsa_circ_291326,RMVar_hsa_circ_338622,RMVar_hsa_circ_161548,RMVar_hsa_circ_161549 115954 RMVar_ID_115954 Human_SNP_ID_814615839 m1A Human chr12 - 20369210 20369210 20369210 ACGCCCCCGCCCCGACCCACGCGCGCGCGCGCACACACACACACACACACACGCACGCACGCTCT ACGCCCCCGCCCCGACCCACGCGCGCGCGCGCGCACACACACACACACACACGCACGCACGCTCT T C AC129102.1 Ensembl:ENSG00000256879 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:20369168..20369327;chr12:20369160..20369262 26863196 MeRIP-seq:(Medium) rs566929213 Functional Loss SNV ICGC 33..33 33 STAD 1 - 115955 RMVar_ID_115955 Human_SNP_ID_814624906 m1A Human chr12 + 57498216 57498216 57498216 GCTCATCACCAGTGCCCTCCCTTACGTCAACAATGTCCCCCACCTTGGGAACATCATTGGTTGTG GCTCATCACCAGTGCCCTCCCTTACGTCAACAGTGTCCCCCACCTTGGGAACATCATTGGTTGTG A G MARS1 Ensembl:ENSG00000166986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57498129..57498295 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_35304,Human_RBP_ID_424719,Human_RBP_ID_8380655,Human_RBP_ID_8783945,Human_RBP_ID_9279093,Human_RBP_ID_17239903,Human_RBP_ID_17472765,Human_RBP_ID_18630491,Human_RBP_ID_22436022,Human_RBP_ID_26806897,Human_RBP_ID_26909776 Human_Splice_Rec_1388318,Human_Splice_Rec_1388319,Human_Splice_Rec_1388356,Human_Splice_Rec_1388380,Human_Splice_Rec_1388381,Human_Splice_Rec_1388450,Human_Splice_Rec_1388456,Human_Splice_Rec_1388457,Human_Splice_Rec_1388476,Human_Splice_Rec_1388477,Human_Splice_Rec_1388516,Human_Splice_Rec_1388517,Human_Splice_Rec_1388554,Human_Splice_Rec_1388555 Human_miRNA_ID_2697450 RMVar_hsa_circ_77258,RMVar_hsa_circ_93971,RMVar_hsa_circ_157658,RMVar_hsa_circ_157659,RMVar_hsa_circ_112516,RMVar_hsa_circ_105310,RMVar_hsa_circ_157661,RMVar_hsa_circ_123043,RMVar_hsa_circ_157663,RMVar_hsa_circ_95441,RMVar_hsa_circ_157662,RMVar_hsa_circ_113933,RMVar_hsa_circ_157664,RMVar_hsa_circ_157667,RMVar_hsa_circ_293316,RMVar_hsa_circ_320893,RMVar_hsa_circ_157665,RMVar_hsa_circ_361972,RMVar_hsa_circ_310671,RMVar_hsa_circ_157668,RMVar_hsa_circ_157666 115956 RMVar_ID_115956 Human_SNP_ID_814646445 m1A Human chr12 - 69258936 69258936 69258936 TTCACATGCGGAGCTGGCGGTGGGGCACCTGGAGGTGGTCCAGGAAGATGCGGAGGAGGAGCTAG TTCACATGCGGAGCTGGCGGTGGGGCACCTGGCGGTGGTCCAGGAAGATGCGGAGGAGGAGCTAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:69258626..69259025;chr12:69258703..69259000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_158152,RMVar_hsa_circ_158153,RMVar_hsa_circ_158154 115957 RMVar_ID_115957 Human_SNP_ID_814659826 m1A Human chr12 - 6904866 6904866 6904866 GCGCAAATCAGCCGGGGAGGGGATTGATCAGTAGTTGCCTGGTTACCACGCCACTTTCCCGTCCC GCGCAAATCAGCCGGGGAGGGGATTGATCAGTTGTTGCCTGGTTACCACGCCACTTTCCCGTCCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6904838..6904940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 115958 RMVar_ID_115958 Human_SNP_ID_814663894 m1A Human chr12 + 31089506 31089506 31089506 GCAGAGAAGCAGGCACGGTAGCCACTGGGACCATGGTGTAGCCGCAGGTGGTCTGGAGAGAGTGA GCAGAGAAGCAGGCACGGTAGCCACTGGGACCGTGGTGTAGCCGCAGGTGGTCTGGAGAGAGTGA A G DDX11 Ensembl:ENSG00000013573 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2075318 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_809413,Human_RBP_ID_872198,Human_RBP_ID_1268792,Human_RBP_ID_3941489,Human_RBP_ID_19056005,Human_RBP_ID_26322758 GWAS_ID_13242,GWAS_ID_13243,GWAS_ID_13244,GWAS_ID_13245,GWAS_ID_13246 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643,RMVar_hsa_circ_25568 115959 RMVar_ID_115959 Human_SNP_ID_814669564 m1A Human chr12 + 753246 753246 753246 CCTCCCCTCATGACTGCGGCGCCTCTGCTGCCACCGCCCGCCCGGCCGCCGCTCGCCGCAGGATG CCTCCCCTCATGACTGCGGCGCCTCTGCTGCCCCCGCCCGCCCGGCCGCCGCTCGCCGCAGGATG A C WNK1 Ensembl:ENSG00000060237 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:753163..753399 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_752827,Human_RBP_ID_876873,Human_RBP_ID_4245938,Human_RBP_ID_8785822,Human_RBP_ID_9278829,Human_RBP_ID_18469293 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 115960 RMVar_ID_115960 Human_SNP_ID_814693931 m1A Human chr12 + 57526242 57526242 57526242 CCTGCTGGGACTCCCCACCCCTGGCCCTTCCCACTCTGATGGAAGCTTTAACCTTTTGGGGTCAG CCTGCTGGGACTCCCCACCCCTGGCCCTTCCCCCTCTGATGGAAGCTTTAACCTTTTGGGGTCAG A C MBD6 Ensembl:ENSG00000166987 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57526191..57526618 32194978 MeRIP-seq:(Medium) rs757745875 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 1 head and neck Human_RBP_ID_3418399,Human_RBP_ID_5127183,Human_RBP_ID_17075149,Human_RBP_ID_18935502 RMVar_hsa_circ_66071 115961 RMVar_ID_115961 Human_SNP_ID_814695121 m1A Human chr12 - 76031295 76031295 76031295 GCTGGGAGGATGCTGGAGAGTAGCGGCTGCAAAGCGCTGAAGGAGGGCGTGCTGGAGAAGCGCAG GCTGGGAGGATGCTGGAGAGTAGCGGCTGCAACGCGCTGAAGGAGGGCGTGCTGGAGAAGCGCAG T G PHLDA1 Ensembl:ENSG00000139289 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:76031250..76031578 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_753782,Human_RBP_ID_811398,Human_RBP_ID_878635,Human_RBP_ID_4246218,Human_RBP_ID_22040643 Human_miRNA_ID_1539321,Human_miRNA_ID_1593387 RMVar_hsa_circ_123121,RMVar_hsa_circ_158349 115962 RMVar_ID_115962 Human_SNP_ID_814705864 m1A Human chr12 - 53462564 53462564 53462564 TTCTAGCCCACAAATGAGAATTTTCTTACCTGACCACCTGCAAAGATGACCGGAGAGCTGGACGG TTCTAGCCCACAAATGAGAATTTTCTTACCTGTCCACCTGCAAAGATGACCGGAGAGCTGGACGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:53462429..53464903;chr12:53462476..53465938;chr12:53462476..53462575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 115963 RMVar_ID_115963 Human_SNP_ID_814707246 m1A Human chr12 + 2885401 2885401 2885401 GCCTCCCAGAAAAAAACGCCGCCAGCCTTCCCAGAAAGCCCCGCTGCTGTTCCACCAACAACCAC GCCTCCCAGAAAAAAACGCCGCCAGCCTTCCCTGAAAGCCCCGCTGCTGTTCCACCAACAACCAC A T RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2885276..2887029 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 3 biliary tract,gallbladder Human_RBP_ID_4246461,Human_RBP_ID_17357484 Human_Splice_Rec_1325113 Human_miRNA_ID_2756662,Human_miRNA_ID_3065933 RMVar_hsa_circ_53065,RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 115964 RMVar_ID_115964 Human_SNP_ID_814709080 m1A Human chr12 - 6922763 6922763 6922763 GCACACTGGGATTACGGAAGTTATGTCCGGCAAAGCGAGCTTCATCCCCCAGCTCTTCCTCAATT GCACACTGGGATTACGGAAGTTATGTCCGGCACAGCGAGCTTCATCCCCCAGCTCTTCCTCAATT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6922751..6922950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 115965 RMVar_ID_115965 Human_SNP_ID_814717663 m1A Human chr12 - 120438152 120438152 120438152 GCTGTGGGCGGGACCGACCCAGCAGCCGAGAAACCGAGGACACACCAACTACCGCCATTTTTGAT GCTGTGGGCGGGACCGACCCAGCAGCCGAGAACCCGAGGACACACCAACTACCGCCATTTTTGAT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:120438101..120438391 26863196 MeRIP-seq:(Medium) rs777475898 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 115966 RMVar_ID_115966 Human_SNP_ID_814718977 m1A Human chr12 - 108561052 108561052 108561052 GAGAGGAGGATGAGGTTAAGGCGGCTAGGACAAGGAGGAAGGTGTTATCGCGGGCTGTGGCCGCT GAGAGGAGGATGAGGTTAAGGCGGCTAGGACAGGGAGGAAGGTGTTATCGCGGGCTGTGGCCGCT T C SART3 Ensembl:ENSG00000075856 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:108560807..108561175 26863196 MeRIP-seq:(Medium) rs1565871444 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_4198970,Human_RBP_ID_9366895,Human_RBP_ID_18410913,Human_RBP_ID_18417328,Human_RBP_ID_26321964,Human_RBP_ID_27807141 115967 RMVar_ID_115967 Human_SNP_ID_814747116 m1A Human chr12 + 49792502 49792502 49792502 CAGTTGTCGGGGTGGGCACATGAGAGGGTCCGAGGAGCTGCCGGCTGCCCTAGTATTGGGGAAGG CAGTTGTCGGGGTGGGCACATGAGAGGGTCCGTGGAGCTGCCGGCTGCCCTAGTATTGGGGAAGG A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49792455..49792532 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung 115968 RMVar_ID_115968 Human_SNP_ID_814747161 m1A Human chr12 + 124940022 124940022 124940022 GCATGCTTTGCACGTATGAGGCCCCGGGTTCAATCCCCGGCATCTCCAGACTTTTCCGCCTTTTT GCATGCTTTGCACGTATGAGGCCCCGGGTTCAGTCCCCGGCATCTCCAGACTTTTCCGCCTTTTT A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, from four datasets;HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs768586678 Functional Loss SNV ICGC 33..33 33 MELA 1 - 115969 RMVar_ID_115969 Human_SNP_ID_814756053 m1A Human chr12 + 52238750 52238750 52238750 GGCCAAGGTGGATGCCCTGAATGATGAGATCAACTTCCTCAGGACCCTCAATGAGACGGTGAGGA GGCCAAGGTGGATGCCCTGAATGATGAGATCAGCTTCCTCAGGACCCTCAATGAGACGGTGAGGA A G KRT7 Ensembl:ENSG00000135480 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:52238676..52238874 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 face Merkel_cell_carcinoma,skin Merkel_cell_carcinoma 2 skin,head and neck Human_RBP_ID_5555397 Human_Splice_Rec_1371726,Human_Splice_Rec_1371727,Human_Splice_Rec_1371742,Human_Splice_Rec_1371743,Human_Splice_Rec_1371745,Human_Splice_Rec_1371747,Human_Splice_Rec_1371753 RMVar_hsa_circ_28774,RMVar_hsa_circ_82510,RMVar_hsa_circ_156661,RMVar_hsa_circ_115454,RMVar_hsa_circ_126393,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662,RMVar_hsa_circ_40173,RMVar_hsa_circ_94882,RMVar_hsa_circ_305750,RMVar_hsa_circ_30207,RMVar_hsa_circ_31227,RMVar_hsa_circ_82390,RMVar_hsa_circ_156663,RMVar_hsa_circ_156664,RMVar_hsa_circ_78719,RMVar_hsa_circ_156665,RMVar_hsa_circ_156666 115970 RMVar_ID_115970 Human_SNP_ID_814766826 m1A Human chr12 + 52237457 52237457 52237457 CAGATTTCACAGCTGCATATGGCGGAGGGGGGACGGGAGCATGGAGGCAAAGCTGCATCAACACC CAGATTTCACAGCTGCATATGGCGGAGGGGGGGCGGGAGCATGGAGGCAAAGCTGCATCAACACC A G KRT7 Ensembl:ENSG00000135480 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52237451..52237637 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_82510,RMVar_hsa_circ_156661,RMVar_hsa_circ_115454,RMVar_hsa_circ_126393,RMVar_hsa_circ_156660,RMVar_hsa_circ_156662 115971 RMVar_ID_115971 Human_SNP_ID_814766962 m1A Human chr12 + 103943230 103943230 103943230 ATGTTGCCAAGGAAGGAGTGAAGTTCGATGAAAGTGAGAAAACTAAGGAGAGTCGTGAAGCAGTT ATGTTGCCAAGGAAGGAGTGAAGTTCGATGAAGGTGAGAAAACTAAGGAGAGTCGTGAAGCAGTT A G HSP90B1 Ensembl:ENSG00000166598 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:103943179..103943346 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_35268,Human_RBP_ID_1463049,Human_RBP_ID_1785187,Human_RBP_ID_2299154,Human_RBP_ID_3390541,Human_RBP_ID_5554509,Human_RBP_ID_6122399,Human_RBP_ID_8363316,Human_RBP_ID_9365455,Human_RBP_ID_11785620,Human_RBP_ID_17669060,Human_RBP_ID_17683162,Human_RBP_ID_22168894,Human_RBP_ID_22756456,Human_RBP_ID_22897276,Human_RBP_ID_23532544,Human_RBP_ID_24543318,Human_RBP_ID_26321913,Human_RBP_ID_26899996,Human_RBP_ID_27807062 Human_Splice_Rec_1416365,Human_Splice_Rec_1416411 RMVar_hsa_circ_2770,RMVar_hsa_circ_121104,RMVar_hsa_circ_86096,RMVar_hsa_circ_159351,RMVar_hsa_circ_62806,RMVar_hsa_circ_368042,RMVar_hsa_circ_159355,RMVar_hsa_circ_70954,RMVar_hsa_circ_342980,RMVar_hsa_circ_348038,RMVar_hsa_circ_81709,RMVar_hsa_circ_159359,RMVar_hsa_circ_98686,RMVar_hsa_circ_117640,RMVar_hsa_circ_159360,RMVar_hsa_circ_108143,RMVar_hsa_circ_159361,RMVar_hsa_circ_51235,RMVar_hsa_circ_91683,RMVar_hsa_circ_159362,RMVar_hsa_circ_159363 115972 RMVar_ID_115972 Human_SNP_ID_814768759 m1A Human chr12 + 76053753 76053753 76053753 TAACAAAAACAGAAAAAACATTTTGTTAAGGTAGTAAAATTAAACTCACCCTGTACAACCCATAA TAACAAAAACAGAAAAAACATTTTGTTAAGGTGGTAAAATTAAACTCACCCTGTACAACCCATAA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:76053751..76053800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 11 lung 115973 RMVar_ID_115973 Human_SNP_ID_814771759 m1A Human chr12 + 98595740 98595740 98595740 GTGTCTTCTCTTACTACAGAGTACAGTTGTGAATTTGGCTCCGCGAAGTATTATGCACTGTGTGG GTGTCTTCTCTTACTACAGAGTACAGTTGTGAGTTTGGCTCCGCGAAGTATTATGCACTGTGTGG A G SLC25A3 Ensembl:ENSG00000075415 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:98595726..98595750 26863196 MeRIP-seq:(Medium) rs761707071 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_431103,Human_RBP_ID_752968,Human_RBP_ID_995289,Human_RBP_ID_1168835,Human_RBP_ID_1271213,Human_RBP_ID_1359000,Human_RBP_ID_1803910,Human_RBP_ID_4260961,Human_RBP_ID_17600510,Human_RBP_ID_17650465,Human_RBP_ID_17685648,Human_RBP_ID_18635526,Human_RBP_ID_19058890,Human_RBP_ID_22437971,Human_RBP_ID_22646790,Human_RBP_ID_22756086,Human_RBP_ID_23207786,Human_RBP_ID_23581427,Human_RBP_ID_25014694,Human_RBP_ID_27219318 Human_Splice_Rec_1411502,Human_Splice_Rec_1411514,Human_Splice_Rec_1411580,Human_Splice_Rec_1411586,Human_Splice_Rec_1411600,Human_Splice_Rec_1411626 RMVar_hsa_circ_117595,RMVar_hsa_circ_45544,RMVar_hsa_circ_378784,RMVar_hsa_circ_159021,RMVar_hsa_circ_282329,RMVar_hsa_circ_362528,RMVar_hsa_circ_159020,RMVar_hsa_circ_284772,RMVar_hsa_circ_159022 115974 RMVar_ID_115974 Human_SNP_ID_814778131 m1A Human chr12 - 4321263 4321263 4321263 AACAGTCAGAGCGAAGCGAGCCATGTTCCCGGAGCCGCGTCCCGTCGGTGGCCCCGCGCCGCGCT AACAGTCAGAGCGAAGCGAGCCATGTTCCCGGGGCCGCGTCCCGTCGGTGGCCCCGCGCCGCGCT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:4321217..4321349 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 3 kidney 115975 RMVar_ID_115975 Human_SNP_ID_814779358 m1A Human chr12 - 110326475 110326475 110326475 GTAAATAAAAACACATTTCATAAAGTACTTACAGAAAACAGCATGTTCTTTTTATCTTGGTTGAC GTAAATAAAAACACATTTCATAAAGTACTTACCGAAAACAGCATGTTCTTTTTATCTTGGTTGAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110326450..110326523 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - 115976 RMVar_ID_115976 Human_SNP_ID_814803858 m1A Human chr12 + 103965899 103965899 103965899 ACGGTAGAAGCCTGGAGGAGGAGCTTGAGTCCAGCCACTGTCTGGGTACTGCCAGCCATCGGGCC ACGGTAGAAGCCTGGAGGAGGAGCTTGAGTCCGGCCACTGTCTGGGTACTGCCAGCCATCGGGCC A G TDG Ensembl:ENSG00000139372 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:103965851..103966010;chr12:103965851..103967894 26863196 MeRIP-seq:(Medium) rs112179075 Functional Loss SNV ICGC,COSMIC 33..33 33 meninges anaplastic,LICA 6 brain Human_RBP_ID_229034,Human_RBP_ID_877662,Human_RBP_ID_9322669,Human_RBP_ID_18410730,Human_RBP_ID_18417322,Human_RBP_ID_22039513,Human_RBP_ID_26321932 RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 115977 RMVar_ID_115977 Human_SNP_ID_814812465 m1A Human chr12 + 53486735 53486735 53486735 GAATTGACTTAAGGAGGGTGAGGCAGAAAGCCAAAAATAGGCCAAGAAGAAGGTTCGAGGGGACA GAATTGACTTAAGGAGGGTGAGGCAGAAAGCCGAAAATAGGCCAAGAAGAAGGTTCGAGGGGACA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53486690..53486845 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas 115978 RMVar_ID_115978 Human_SNP_ID_814820641 m1A Human chr12 + 6538195 6538195 6538195 AGGAGTAAGACCCCTGGACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTG AGGAGTAAGACCCCTGGACCACCAGCCCCAGCGAGAGCACAAGAGGAAGAGAGAGACCCTCACTG A G GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6538155..6538320 26863196 MeRIP-seq:(Medium) rs770280504 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_426007,Human_RBP_ID_1476008,Human_RBP_ID_1799247,Human_RBP_ID_3411546,Human_RBP_ID_6209879,Human_RBP_ID_12009544,Human_RBP_ID_17240176,Human_RBP_ID_17355709,Human_RBP_ID_17650301,Human_RBP_ID_18188702,Human_RBP_ID_18631586,Human_RBP_ID_22435753,Human_RBP_ID_22532409,Human_RBP_ID_27424469 Human_Splice_Rec_1328616,Human_Splice_Rec_1328632,Human_Splice_Rec_1328662,Human_Splice_Rec_1328676,Human_Splice_Rec_1328688,Human_Splice_Rec_1328702,Human_Splice_Rec_1328708,Human_Splice_Rec_1328722,Human_Splice_Rec_1328734 Human_miRNA_ID_2684866 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 115979 RMVar_ID_115979 Human_SNP_ID_814826058 m1A Human chr12 - 120446281 120446281 120446281 TCGCTGGTTCGCCGAGAAATTTCTCAAGGGGGACAGCTCCGGGGACCCGTGCACCGACCTCTTCA TCGCTGGTTCGCCGAGAAATTTCTCAAGGGGGGCAGCTCCGGGGACCCGTGCACCGACCTCTTCA T C TRIAP1 Ensembl:ENSG00000170855 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120446226..120446359 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_811641,Human_RBP_ID_4205121,Human_RBP_ID_5491016,Human_RBP_ID_6142190,Human_RBP_ID_22437477 Human_Splice_Rec_1433063 RMVar_hsa_circ_92819,RMVar_hsa_circ_160781 115980 RMVar_ID_115980 Human_SNP_ID_814827091 m1A Human chr12 - 32726580 32726580 32726580 ATGATGCTGAAGCTATCCTTGCTGCAGACTTCAAAATTGGTCACTTTTTACGTGAGCATACAATC ATGATGCTGAAGCTATCCTTGCTGCAGACTTCGAAATTGGTCACTTTTTACGTGAGCATACAATC T C AC084824.2 Ensembl:ENSG00000257511 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs893151551 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 18 haematopoietic and lymphoid tissue Human_RBP_ID_23556771,Human_RBP_ID_26415301,Human_RBP_ID_26905773 115981 RMVar_ID_115981 Human_SNP_ID_814834460 m1A Human chr12 + 27420509 27420509 27420509 CAGAGGGGGGCCTGGGAGACCCTGGGGACTTCAGTGACATCCAGTGGACCCTCTAGCCTTTGATT CAGAGGGGGGCCTGGGAGACCCTGGGGACTTCGGTGACATCCAGTGGACCCTCTAGCCTTTGATT A G ARNTL2 Ensembl:ENSG00000029153 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:27420426..27420600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 7 stomach RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 115982 RMVar_ID_115982 Human_SNP_ID_814837753 m1A Human chr12 - 110465214 110465214 110465214 GCTTTAACCTCTCATGCCTTGTGACATTACAGAGCACCTACTGTGCCACCATGGTCCAGCACTGT GCTTTAACCTCTCATGCCTTGTGACATTACAGTGCACCTACTGTGCCACCATGGTCCAGCACTGT T A GPN3 Ensembl:ENSG00000111231 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:110465177..110468189 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_1355984,Human_RBP_ID_4246982,Human_RBP_ID_5315048,Human_RBP_ID_9279206,Human_RBP_ID_22438030 Human_Splice_Rec_1423246,Human_Splice_Rec_1423260,Human_Splice_Rec_1423274,Human_Splice_Rec_1423298,Human_Splice_Rec_1423308,Human_Splice_Rec_1423312,Human_Splice_Rec_1423316 115983 RMVar_ID_115983 Human_SNP_ID_814848750 m1A Human chr12 + 6537003 6537003 6537003 GGAGTCCACTGGCGTCTTCACCACCATGGAGAAGGCTGGGGTGAGTGCAGGAGGGCCCGCGGGAG GGAGTCCACTGGCGTCTTCACCACCATGGAGAGGGCTGGGGTGAGTGCAGGAGGGCCCGCGGGAG A G GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6537001..6537050 32194978 MeRIP-seq:(Medium) rs1361841795 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus Human_RBP_ID_34189,Human_RBP_ID_425982,Human_RBP_ID_877285,Human_RBP_ID_993964,Human_RBP_ID_17240166,Human_RBP_ID_17355703,Human_RBP_ID_18188685,Human_RBP_ID_18631572,Human_RBP_ID_19057490,Human_RBP_ID_22435746,Human_RBP_ID_22755810 Human_Splice_Rec_1328608,Human_Splice_Rec_1328609,Human_Splice_Rec_1328624,Human_Splice_Rec_1328625,Human_Splice_Rec_1328640,Human_Splice_Rec_1328641,Human_Splice_Rec_1328654,Human_Splice_Rec_1328655,Human_Splice_Rec_1328669,Human_Splice_Rec_1328681,Human_Splice_Rec_1328694,Human_Splice_Rec_1328695,Human_Splice_Rec_1328714,Human_Splice_Rec_1328715,Human_Splice_Rec_1328726,Human_Splice_Rec_1328727 RMVar_hsa_circ_88042,RMVar_hsa_circ_154536,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_105081,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_125986,RMVar_hsa_circ_154542,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_154541,RMVar_hsa_circ_120781,RMVar_hsa_circ_96003,RMVar_hsa_circ_154547,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_154546,RMVar_hsa_circ_120258,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_374391,RMVar_hsa_circ_124027,RMVar_hsa_circ_88412,RMVar_hsa_circ_154552,RMVar_hsa_circ_154554,RMVar_hsa_circ_49293,RMVar_hsa_circ_154553,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551,RMVar_hsa_circ_122873,RMVar_hsa_circ_378260,RMVar_hsa_circ_154556,RMVar_hsa_circ_89669,RMVar_hsa_circ_111060,RMVar_hsa_circ_154558,RMVar_hsa_circ_154559,RMVar_hsa_circ_154560,RMVar_hsa_circ_154557 115984 RMVar_ID_115984 Human_SNP_ID_814853072 m1A Human chr12 + 49272509 49272509 49272509 TGCCTTCATGGTAGACAATGAGGCCATCTATGACATCTGTCGTAGAAACCTCGATATCGAGCGCC TGCCTTCATGGTAGACAATGAGGCCATCTATGGCATCTGTCGTAGAAACCTCGATATCGAGCGCC A G TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus Human_miRNA_ID_2534634,Human_miRNA_ID_2536366 RMVar_hsa_circ_118502,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156317,RMVar_hsa_circ_107279,RMVar_hsa_circ_83896,RMVar_hsa_circ_156318,RMVar_hsa_circ_156319 115985 RMVar_ID_115985 Human_SNP_ID_814855747 m1A Human chr12 - 53719769 53719769 53719769 CGGGAACAAGAGAAGCTCCTTGGGCAACTGAAAGAAGTACAAGCAGACAAGGAGCAAAGTGAGGT CGGGAACAAGAGAAGCTCCTTGGGCAACTGAAGGAAGTACAAGCAGACAAGGAGCAAAGTGAGGT T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53719751..53719825 26863196 MeRIP-seq:(Medium) rs1467359323 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_874626,Human_RBP_ID_27806639 Human_Splice_Rec_1376354,Human_Splice_Rec_1376355,Human_Splice_Rec_1376382,Human_Splice_Rec_1376383,Human_Splice_Rec_1376420,Human_Splice_Rec_1376421,Human_Splice_Rec_1376446,Human_Splice_Rec_1376447,Human_Splice_Rec_1376472,Human_Splice_Rec_1376473,Human_Splice_Rec_1376491,Human_Splice_Rec_1376504 RMVar_hsa_circ_23912,RMVar_hsa_circ_277548,RMVar_hsa_circ_157005 115986 RMVar_ID_115986 Human_SNP_ID_814859262 m1A Human chr12 + 131395654 131395644 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATG__________TGGTGATGGTGATGGTGATGATGGTGATGGTG GGTGATGATGA G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 24..33 33 SKCA 1 - 115987 RMVar_ID_115987 Human_SNP_ID_814865919 m1A Human chr12 - 6200489 6200489 6200489 TGGTGCCTCCTTTGACCGGCATGGTGAGGGCTAACTTAGCCTGGGCCGAACGGGTGCGGGACTGG TGGTGCCTCCTTTGACCGGCATGGTGAGGGCTCACTTAGCCTGGGCCGAACGGGTGCGGGACTGG T G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:6200388..6200490 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 115988 RMVar_ID_115988 Human_SNP_ID_814866323 m1A Human chr12 - 30629601 30629601 30629601 TTTATTCAGCAAAATGAAAACGTATCTTCAGAACTTAACATATTACTGGATGTGATACAGATTTT TTTATTCAGCAAAATGAAAACGTATCTTCAGAGCTTAACATATTACTGGATGTGATACAGATTTT T C IPO8 Ensembl:ENSG00000133704 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs75560605 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17470546 RMVar_hsa_circ_268889 115989 RMVar_ID_115989 Human_SNP_ID_814868931 m1A Human chr12 + 124911831 124911831 124911831 AGCTGTTTCCCAGCAAAGATCAACCTCTGCTGATCAGGAGGGATGCCTTCCTTATCTTGGATCTT AGCTGTTTCCCAGCAAAGATCAACCTCTGCTGGTCAGGAGGGATGCCTTCCTTATCTTGGATCTT A G HSALNG0094859 RNACentral:URS0000EB0431 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124911693..124911866 26863196 MeRIP-seq:(Medium) rs16918544 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,oesophagus adenocarcinoma,liver neoplasm,ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 25 liver,oesophagus,prostate,haematopoietic and lymphoid tissue GWAS_ID_12087 115990 RMVar_ID_115990 Human_SNP_ID_814870983 m1A Human chr12 + 56136861 56136861 56136861 ACCAGTGGTTCCAGCTCAGCAGCTCTGGTCCAAACTCCAGACTCTATATGAAACTAGTCATGAGG ACCAGTGGTTCCAGCTCAGCAGCTCTGGTCCACACTCCAGACTCTATATGAAACTAGTCATGAGG A C - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 115991 RMVar_ID_115991 Human_SNP_ID_814892230 m1A Human chr12 + 55726172 55726171 55726172 TCGTTGAAATTAATCCCACAGCCCACAGTAACATTAATGCAGCAGGAGTCGGGGACTCGGTTCTT TCGTTGAAATTAATCCCACAGCCCACAGTAAC_TTAATGCAGCAGGAGTCGGGGACTCGGTTCTT CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55726101..55726275 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 PRAD 1 - 115992 RMVar_ID_115992 Human_SNP_ID_814926725 m1A Human chr12 - 132572530 132572530 132572530 CAGTCCCGGGATGGCAGGAGGGAAGGACGGGAAGAACTGTAAGAGAAGGAGAGCGGATGGAGGGG CAGTCCCGGGATGGCAGGAGGGAAGGACGGGAGGAACTGTAAGAGAAGGAGAGCGGATGGAGGGG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132572239..132572571 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 115993 RMVar_ID_115993 Human_SNP_ID_814951180 m1A Human chr12 - 7190436 7190436 7190436 GAAGGGCCTTGTCCTGGGTGAAGTGCCCGGCGAGCTTCATGAGCGGGTTGGCACCCCCGCATTCG GAAGGGCCTTGTCCTGGGTGAAGTGCCCGGCGGGCTTCATGAGCGGGTTGGCACCCCCGCATTCG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7190385..7190585 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 8 uterus 115994 RMVar_ID_115994 Human_SNP_ID_814966027 m1A Human chr12 - 52952205 52952205 52952205 CCCTCTGCCCGGGTCTGTGCCAGCTCTGACTCAAGGTGCAGCAGGATCCCGTTGAGCTGCTCCAT CCCTCTGCCCGGGTCTGTGCCAGCTCTGACTCCAGGTGCAGCAGGATCCCGTTGAGCTGCTCCAT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:52952126..52952357 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver 115995 RMVar_ID_115995 Human_SNP_ID_814971268 m1A Human chr12 - 132786557 132786557 132786557 AGCTTCCTCCTGTGTCTCCCTCATGACACCCCAGGGCCATCACGGAACAGAAGCAGAAGATGAGG AGCTTCCTCCTGTGTCTCCCTCATGACACCCCTGGGCCATCACGGAACAGAAGCAGAAGATGAGG T A GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:132786524..132786725 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver neoplasm 4 liver Human_RBP_ID_878201 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_60268,RMVar_hsa_circ_112930,RMVar_hsa_circ_75106,RMVar_hsa_circ_161884,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_276536,RMVar_hsa_circ_375367,RMVar_hsa_circ_161888,RMVar_hsa_circ_1421,RMVar_hsa_circ_108679,RMVar_hsa_circ_161889,RMVar_hsa_circ_161890 115996 RMVar_ID_115996 Human_SNP_ID_814988790 m1A Human chr12 - 51240394 51240394 51240394 GAGCCTGAGGAAGATGCAAGGTCTGAGGGTATACTGGATTCCCAGGAGGCTGCACAGGGTAGGTT GAGCCTGAGGAAGATGCAAGGTCTGAGGGTATGCTGGATTCCCAGGAGGCTGCACAGGGTAGGTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:51240301..51240490 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 10 stomach 115997 RMVar_ID_115997 Human_SNP_ID_814997211 m1A Human chr12 + 51195943 51195942 51195943 AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCCACCCCCCACCCCCCCCAGCCCCTGTACCTCACT AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCC_CCCCCCACCCCCCCCAGCCCCTGTACCTCACT CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:51195942..51196052 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - 115998 RMVar_ID_115998 Human_SNP_ID_815007043 m1A Human chr12 + 56612052 56612052 56612052 TGCGGGACAAACTTCTGGAGAGATTTCTGGGGAGGCTGCTGGAGAAACCACTAGGGAGACTGCTG TGCGGGACAAACTTCTGGAGAGATTTCTGGGGGGGCTGCTGGAGAAACCACTAGGGAGACTGCTG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56612001..56612075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma,UCEC 5 pancreas RMVar_hsa_circ_157424 115999 RMVar_ID_115999 Human_SNP_ID_815025740 m1A Human chr12 + 54011338 54011338 54011338 TGAGGAGAAGGTGGAGGAAGAAGGAAATGAGGAAGAGGAGAAAGAAGAGGAGGAAAAGGAAGAAA TGAGGAGAAGGTGGAGGAAGAAGGAAATGAGGGAGAGGAGAAAGAAGAGGAGGAAAAGGAAGAAA A G HOXC8,AC012531.3,HOXC6 Ensembl:ENSG00000037965,Ensembl:ENSG00000273049,Ensembl:ENSG00000197757 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54011291..54011397 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4229625 116000 RMVar_ID_116000 Human_SNP_ID_815025921 m1A Human chr12 - 108564352 108564352 108564352 TCATTACGTCACCACATGCTGGAGCCCCCACCAGTCCAGTTCCAACATTTTTAGATGTCTTGTCA TCATTACGTCACCACATGCTGGAGCCCCCACCCGTCCAGTTCCAACATTTTTAGATGTCTTGTCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:108564301..108564400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116001 RMVar_ID_116001 Human_SNP_ID_815044794 m1A Human chr12 - 6200473 6200473 6200473 CGGCATGGTGAGGGCTAACTTAGCCTGGGCCGAACGGGTGCGGGACTGGGGGGCGCGCGCAGCTG CGGCATGGTGAGGGCTAACTTAGCCTGGGCCGGACGGGTGCGGGACTGGGGGGCGCGCGCAGCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:6200426..6200525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116002 RMVar_ID_116002 Human_SNP_ID_815049015 m1A Human chr12 + 7203526 7203526 7203526 TGAGGCCCACCCCTGGCTTTCTGACTATGATGACCTTACGTCAGCTACCTATGATAAGGTGAGGT TGAGGCCCACCCCTGGCTTTCTGACTATGATGTCCTTACGTCAGCTACCTATGATAAGGTGAGGT A T PEX5 Ensembl:ENSG00000139197 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:7203476..7203525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_1334454,Human_Splice_Rec_1334455,Human_Splice_Rec_1334490,Human_Splice_Rec_1334491,Human_Splice_Rec_1334540,Human_Splice_Rec_1334541,Human_Splice_Rec_1334574,Human_Splice_Rec_1334592,Human_Splice_Rec_1334593,Human_Splice_Rec_1334622,Human_Splice_Rec_1334623,Human_Splice_Rec_1334650,Human_Splice_Rec_1334651,Human_Splice_Rec_1334688,Human_Splice_Rec_1334689 RMVar_hsa_circ_117310,RMVar_hsa_circ_154713,RMVar_hsa_circ_348665,RMVar_hsa_circ_376073,RMVar_hsa_circ_154714,RMVar_hsa_circ_346668,RMVar_hsa_circ_154715,RMVar_hsa_circ_330147,RMVar_hsa_circ_369706,RMVar_hsa_circ_26077,RMVar_hsa_circ_154717,RMVar_hsa_circ_154718 116003 RMVar_ID_116003 Human_SNP_ID_815058143 m1A Human chr12 - 121857434 121857434 121857434 CCCTCATGAACCCTGCTGCAACCCTGTGATTCAGGCCACGTCATTCTACTGCAGCAAGATGGGCT CCCTCATGAACCCTGCTGCAACCCTGTGATTCGGGCCACGTCATTCTACTGCAGCAAGATGGGCT T C HPD Ensembl:ENSG00000158104 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:121857404..121857498 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_22538961 RMVar_hsa_circ_74191,RMVar_hsa_circ_361490 116004 RMVar_ID_116004 Human_SNP_ID_815065808 m1A Human chr12 - 118068478 118068478 118068478 AGGGGAACAGGAGGGAGCACGTGAGAGAGAGGAGTTGCCAAAAGAAATACCTAAGCAGGACCACA AGGGGAACAGGAGGGAGCACGTGAGAGAGAGGGGTTGCCAAAAGAAATACCTAAGCAGGACCACA T C VSIG10 Ensembl:ENSG00000176834 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:118068428..118068562 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_95409,RMVar_hsa_circ_86207,RMVar_hsa_circ_104975,RMVar_hsa_circ_160555,RMVar_hsa_circ_160556,RMVar_hsa_circ_160557 116005 RMVar_ID_116005 Human_SNP_ID_815066542 m1A Human chr12 - 120465714 120465714 120465714 ATGGCCAGTGTCGGCTTCGTGTGGAGTTCCCCAGGACTTATGGAGGTCGGGGTGGGTGGCCCCGT ATGGCCAGTGTCGGCTTCGTGTGGAGTTCCCCGGGACTTATGGAGGTCGGGGTGGGTGGCCCCGT T C SRSF9 Ensembl:ENSG00000111786 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:120465552..120469725 26863196 MeRIP-seq:(Medium) rs1256559379 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_412445,Human_RBP_ID_990076,Human_RBP_ID_1465991,Human_RBP_ID_4205232,Human_RBP_ID_5348819,Human_RBP_ID_6142458,Human_RBP_ID_8777003,Human_RBP_ID_9012208,Human_RBP_ID_9279331,Human_RBP_ID_9322749,Human_RBP_ID_11843095,Human_RBP_ID_17650869,Human_RBP_ID_17811015,Human_RBP_ID_22170585,Human_RBP_ID_22793276,Human_RBP_ID_23125180,Human_RBP_ID_23542141,Human_RBP_ID_26322157,Human_RBP_ID_26902077,Human_RBP_ID_27210825,Human_RBP_ID_27623731 Human_Splice_Rec_1433086,Human_Splice_Rec_1433087,Human_Splice_Rec_1433094,Human_Splice_Rec_1433095,Human_Splice_Rec_1433102,Human_Splice_Rec_1433106 116006 RMVar_ID_116006 Human_SNP_ID_815075495 m1A Human chr12 + 107685860 107685860 107685860 GGCAGCAGTGCGGTCGTGGTCCCTCCCTATGCAGCCTGGTTTCTAGCGTGACACGCCCTTGACTT GGCAGCAGTGCGGTCGTGGTCCCTCCCTATGCCGCCTGGTTTCTAGCGTGACACGCCCTTGACTT A C PWP1 Ensembl:ENSG00000136045 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:107685801..107685975 26863196 MeRIP-seq:(Medium) rs1205286082 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_753730,Human_RBP_ID_4246949,Human_RBP_ID_8787351,Human_RBP_ID_9279187,Human_RBP_ID_11793887,Human_RBP_ID_18616533,Human_RBP_ID_26321943,Human_RBP_ID_26900261 Human_miRNA_ID_2093367 RMVar_hsa_circ_94912,RMVar_hsa_circ_111878,RMVar_hsa_circ_159579,RMVar_hsa_circ_87674,RMVar_hsa_circ_159580,RMVar_hsa_circ_159578 116007 RMVar_ID_116007 Human_SNP_ID_815090194 m1A Human chr12 + 49129552 49129552 49129552 TCTACAAACACAGCCCGGGGCACGTGCTTGCCAGCGCCCGTCTCACTGAAGAAGGTGTTGAAGGA TCTACAAACACAGCCCGGGGCACGTGCTTGCCTGCGCCCGTCTCACTGAAGAAGGTGTTGAAGGA A T AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:49129478..49129595 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 116008 RMVar_ID_116008 Human_SNP_ID_815092119 m1A Human chr12 - 120198739 120198739 120198739 GGTGTTTACTGCCCCACTATTATCTGGTTCAGAGTGATGTGCAGCTGATCAAGACTGGAGACAAA GGTGTTTACTGCCCCACTATTATCTGGTTCAGCGTGATGTGCAGCTGATCAAGACTGGAGACAAA T G RPLP0 Ensembl:ENSG00000089157 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:120198718..120198862 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_809726,Human_RBP_ID_1465850,Human_RBP_ID_1788632,Human_RBP_ID_5348814,Human_RBP_ID_6141906,Human_RBP_ID_8247491,Human_RBP_ID_11841717,Human_RBP_ID_18256035,Human_RBP_ID_22170501,Human_RBP_ID_22899397,Human_RBP_ID_23541875,Human_RBP_ID_26806197 Human_Splice_Rec_1432426,Human_Splice_Rec_1432440,Human_Splice_Rec_1432478,Human_Splice_Rec_1432492,Human_Splice_Rec_1432506,Human_Splice_Rec_1432520,Human_Splice_Rec_1432530,Human_Splice_Rec_1432542,Human_Splice_Rec_1432552,Human_Splice_Rec_1432562,Human_Splice_Rec_1432574,Human_Splice_Rec_1432598,Human_Splice_Rec_1432606 RMVar_hsa_circ_125232,RMVar_hsa_circ_82853,RMVar_hsa_circ_92970,RMVar_hsa_circ_160753,RMVar_hsa_circ_126466,RMVar_hsa_circ_349792,RMVar_hsa_circ_371138,RMVar_hsa_circ_160755,RMVar_hsa_circ_160756,RMVar_hsa_circ_160754,RMVar_hsa_circ_335431,RMVar_hsa_circ_160758,RMVar_hsa_circ_82228,RMVar_hsa_circ_101737,RMVar_hsa_circ_160760,RMVar_hsa_circ_160761,RMVar_hsa_circ_160759 116009 RMVar_ID_116009 Human_SNP_ID_815094937 m1A Human chr12 + 57512856 57512856 57512856 CACGGGGATCCCTGCTGACATCTGGCGCTTCTATCTGCTGTACATTCGGCCTGAGGGCCAGGACA CACGGGGATCCCTGCTGACATCTGGCGCTTCTGTCTGCTGTACATTCGGCCTGAGGGCCAGGACA A G MARS1 Ensembl:ENSG00000166986 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57512751..57512975 32194978 MeRIP-seq:(Medium) rs777332933 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_424738,Human_RBP_ID_754050,Human_RBP_ID_1475080,Human_RBP_ID_3409951,Human_RBP_ID_4257991,Human_RBP_ID_8068784,Human_RBP_ID_8380677,Human_RBP_ID_8783969,Human_RBP_ID_9255529,Human_RBP_ID_9278335,Human_RBP_ID_17239908,Human_RBP_ID_17472767,Human_RBP_ID_17823650,Human_RBP_ID_18262479,Human_RBP_ID_18630526,Human_RBP_ID_22794931,Human_RBP_ID_27423940 Human_miRNA_ID_1426082 RMVar_hsa_circ_15567,RMVar_hsa_circ_361972,RMVar_hsa_circ_94821,RMVar_hsa_circ_123367,RMVar_hsa_circ_157669,RMVar_hsa_circ_376396,RMVar_hsa_circ_373799,RMVar_hsa_circ_157675,RMVar_hsa_circ_157677,RMVar_hsa_circ_117871,RMVar_hsa_circ_157676,RMVar_hsa_circ_157674,RMVar_hsa_circ_346254,RMVar_hsa_circ_24304 116010 RMVar_ID_116010 Human_SNP_ID_815095085 m1A Human chr12 - 46188954 46188953 46188954 GTGACGAAGGCCACTGAAACCCGCCGAGAAAAAGAAACATCCCTGTTGTCTGCTCAGTCAAGTCC GTGACGAAGGCCACTGAAACCCGCCGAGAAAA_GAAACATCCCTGTTGTCTGCTCAGTCAAGTCC CT C SLC38A1 Ensembl:ENSG00000111371 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:46188905..46189032 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 STAD 1 - Human_RBP_ID_419787,Human_RBP_ID_4254791,Human_RBP_ID_11942903,Human_RBP_ID_22757168,Human_RBP_ID_22912150,Human_RBP_ID_24971259 RMVar_hsa_circ_156085,RMVar_hsa_circ_105387 116011 RMVar_ID_116011 Human_SNP_ID_815096338 m1A Human chr12 + 57098406 57098406 57098406 AGAGTGGACAGAAGAGAAGAAGACAGGCTGTTAGCATTTGCTGCTCCTTTCTCACAGAAGAGCCT AGAGTGGACAGAAGAGAAGAAGACAGGCTGTTGGCATTTGCTGCTCCTTTCTCACAGAAGAGCCT A G NONHSAG011408.2 RNACentral:URS00008B4182 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:57098399..57098600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 7 large intestine 116012 RMVar_ID_116012 Human_SNP_ID_815097770 m1A Human chr12 + 49763125 49763125 49763125 TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCAACCCCATCTGTAGCCTCTTCCTCTACTCAGGCA TCCTGGGGTTCCCCTCACTCCCTTTTTTGTCACCCCCATCTGTAGCCTCTTCCTCTACTCAGGCA A C TMBIM6 Ensembl:ENSG00000139644 Protein coding 3'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49763076..49763125 26863196 MeRIP-seq:(Medium) rs74087196 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_269472,Human_RBP_ID_421080,Human_RBP_ID_1083022,Human_RBP_ID_1167052,Human_RBP_ID_1357710,Human_RBP_ID_1472799,Human_RBP_ID_1796193,Human_RBP_ID_2340699,Human_RBP_ID_3407208,Human_RBP_ID_4225776,Human_RBP_ID_6191737,Human_RBP_ID_8068354,Human_RBP_ID_8177894,Human_RBP_ID_8377505,Human_RBP_ID_11958940,Human_RBP_ID_17238788,Human_RBP_ID_17354574,Human_RBP_ID_17471625,Human_RBP_ID_17820682,Human_RBP_ID_18206345,Human_RBP_ID_18627870,Human_RBP_ID_18935236,Human_RBP_ID_19775946,Human_RBP_ID_22383294,Human_RBP_ID_22794297,Human_RBP_ID_22904704,Human_RBP_ID_23157703,Human_RBP_ID_23562356,Human_RBP_ID_24407208,Human_RBP_ID_24466552,Human_RBP_ID_24975166,Human_RBP_ID_26416492,Human_RBP_ID_26907317,Human_RBP_ID_27215020,Human_RBP_ID_27422480 Human_miRNA_ID_1531690 RMVar_hsa_circ_123454,RMVar_hsa_circ_156369,RMVar_hsa_circ_156372,RMVar_hsa_circ_125329 116013 RMVar_ID_116013 Human_SNP_ID_815111029 m1A Human chr12 - 57234084 57234084 57234084 ACTCACCAGTCTTGCTCTTCACCTCTAAGCCAATGTTGACCCCTTCATCTATAAAGTCCACAACT ACTCACCAGTCTTGCTCTTCACCTCTAAGCCAGTGTTGACCCCTTCATCTATAAAGTCCACAACT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57234007..57234117 26863196 MeRIP-seq:(Medium) rs1294243777 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 5 liver 116014 RMVar_ID_116014 Human_SNP_ID_815118721 m1A Human chr12 + 752757 752757 752757 CTAGGTCTCCTCTCCTCTTGCCTCAGAGAAGCAGCGGAGCTCGGGCCCCGCGGTGAGCGGCCCTC CTAGGTCTCCTCTCCTCTTGCCTCAGAGAAGCGGCGGAGCTCGGGCCCCGCGGTGAGCGGCCCTC A G WNK1 Ensembl:ENSG00000060237 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:752601..752988 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_36353,Human_RBP_ID_229661,Human_RBP_ID_4245933,Human_RBP_ID_9322396,Human_RBP_ID_22532403 116015 RMVar_ID_116015 Human_SNP_ID_815123993 m1A Human chr12 - 48923801 48923801 48923801 ATTCCTTCTCACTTGGCCTATGGAAAACGGGGATTTCCACCATCTGTCCCAGGTAATCTGACTAG ATTCCTTCTCACTTGGCCTATGGAAAACGGGGTTTTCCACCATCTGTCCCAGGTAATCTGACTAG T A AC073610.2,FKBP11 Ensembl:ENSG00000272822,Ensembl:ENSG00000134285 Protein coding,Protein coding intron,exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48923798..48923898 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_36711,Human_RBP_ID_420551,Human_RBP_ID_2339609,Human_RBP_ID_18627310 Human_Splice_Rec_1363308,Human_Splice_Rec_1363309,Human_Splice_Rec_1363316,Human_Splice_Rec_1363317,Human_Splice_Rec_1363323,Human_Splice_Rec_1363338,Human_Splice_Rec_1363339,Human_Splice_Rec_1363348,Human_Splice_Rec_1363349,Human_Splice_Rec_1363358,Human_Splice_Rec_1363359,Human_Splice_Rec_1363368,Human_Splice_Rec_1363369,Human_Splice_Rec_1363374,Human_Splice_Rec_1363382 RMVar_hsa_circ_32157,RMVar_hsa_circ_110977,RMVar_hsa_circ_15433,RMVar_hsa_circ_29062,RMVar_hsa_circ_156234 116016 RMVar_ID_116016 Human_SNP_ID_815132993 m1A Human chr12 + 56725172 56725172 56725172 AGTAGGAACCCTGTGGCCCAGTAAAGCCTCCAACTCTCCTTAACTCTCAGTCCCCGGGGCGGCTT AGTAGGAACCCTGTGGCCCAGTAAAGCCTCCATCTCTCCTTAACTCTCAGTCCCCGGGGCGGCTT A T - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:56725170..56725283 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116017 RMVar_ID_116017 Human_SNP_ID_815139173 m1A Human chr12 - 293048 293048 293048 ACTTTTTGGAGAAGGAAAACAGAAGTCCAAGGAGTTAAAGAAAATGGACAAACCTAGAAAGAAGA ACTTTTTGGAGAAGGAAAACAGAAGTCCAAGGCGTTAAAGAAAATGGACAAACCTAGAAAGAAGA T G KDM5A Ensembl:ENSG00000073614 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:292787..297138 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_36390,Human_RBP_ID_810116 RMVar_hsa_circ_29544,RMVar_hsa_circ_277817,RMVar_hsa_circ_343114,RMVar_hsa_circ_339765,RMVar_hsa_circ_268453,RMVar_hsa_circ_154142,RMVar_hsa_circ_154143 116018 RMVar_ID_116018 Human_SNP_ID_815151627 m1A Human chr12 + 53321498 53321498 53321498 CTTGCCGGTTCGCAGGACGTCTGCAGTCGGCAAACTCCTGGCCGGAACGGCACAGACCGCACTCC CTTGCCGGTTCGCAGGACGTCTGCAGTCGGCATACTCCTGGCCGGAACGGCACAGACCGCACTCC A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53321356..53321557 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 116019 RMVar_ID_116019 Human_SNP_ID_815154807 m1A Human chr12 + 57517101 57517101 57517101 CTGGAGAGTGAGGGCTCTGGGAGGTGCTTGTGACCTCTGCTGGTTCTGGCTCCTCCTCAGTCAGC CTGGAGAGTGAGGGCTCTGGGAGGTGCTTGTGGCCTCTGCTGGTTCTGGCTCCTCCTCAGTCAGC A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57517051..57517175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_11995416 116020 RMVar_ID_116020 Human_SNP_ID_815155208 m1A Human chr12 - 111361877 111361877 111361877 CTCCTTGACTGCATCCTTCAGTCTTGGCCCCTAGGCCTGGGGCCCCTTGGGAGCTTGCCTGACCT CTCCTTGACTGCATCCTTCAGTCTTGGCCCCTGGGCCTGGGGCCCCTTGGGAGCTTGCCTGACCT T C PHETA1 Ensembl:ENSG00000198324 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs874286 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_miRNA_ID_109227,Human_miRNA_ID_836595 116021 RMVar_ID_116021 Human_SNP_ID_815172162 m1A Human chr12 - 6200507 6200507 6200507 GCAGGTATTTGATGCACTTGGTGCCTCCTTTGACCGGCATGGTGAGGGCTAACTTAGCCTGGGCC GCAGGTATTTGATGCACTTGGTGCCTCCTTTGTCCGGCATGGTGAGGGCTAACTTAGCCTGGGCC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6200457..6200558 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 116022 RMVar_ID_116022 Human_SNP_ID_815176733 m1A Human chr12 + 51195943 51195943 51195943 AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCCACCCCCCACCCCCCCCAGCCCCTGTACCTCACT AGCAGCCGGTGCCAGATAGCAGAGCCTGCCCCCCCCCCCACCCCCCCCAGCCCCTGTACCTCACT A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:51195942..51196052 26863196 MeRIP-seq:(Medium) rs765266326 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116023 RMVar_ID_116023 Human_SNP_ID_815179940 m1A Human chr12 - 132649417 132649417 132649417 GCCCGCAGGAAGAGGCAGCGTCTGGAGTCGGCAGAGGGTGTGCTCAGGCCCGGGGCCATCCGGGA GCCCGCAGGAAGAGGCAGCGTCTGGAGTCGGCGGAGGGTGTGCTCAGGCCCGGGGCCATCCGGGA T C POLE Ensembl:ENSG00000177084 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132649366..132649877 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_229320,Human_RBP_ID_875533,Human_RBP_ID_5521919,Human_RBP_ID_18469279,Human_RBP_ID_18978347 Human_Splice_Rec_1446532,Human_Splice_Rec_1446612,Human_Splice_Rec_1446708,Human_Splice_Rec_1446802,Human_Splice_Rec_1446898,Human_Splice_Rec_1446992,Human_Splice_Rec_1446996 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_80892,RMVar_hsa_circ_87287,RMVar_hsa_circ_161799,RMVar_hsa_circ_161800,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815,RMVar_hsa_circ_106863,RMVar_hsa_circ_105628,RMVar_hsa_circ_120801,RMVar_hsa_circ_161816,RMVar_hsa_circ_111490,RMVar_hsa_circ_161817,RMVar_hsa_circ_161819,RMVar_hsa_circ_77366,RMVar_hsa_circ_96215,RMVar_hsa_circ_161820,RMVar_hsa_circ_161821,RMVar_hsa_circ_113950,RMVar_hsa_circ_161818,RMVar_hsa_circ_85516,RMVar_hsa_circ_3208,RMVar_hsa_circ_93083,RMVar_hsa_circ_161822,RMVar_hsa_circ_19838,RMVar_hsa_circ_161823,RMVar_hsa_circ_95609,RMVar_hsa_circ_161826,RMVar_hsa_circ_86964,RMVar_hsa_circ_161827,RMVar_hsa_circ_161825,RMVar_hsa_circ_24861 116024 RMVar_ID_116024 Human_SNP_ID_815187873 m1A Human chr12 - 124913007 124913007 124913007 GTCGAGCCCAGTGACACTATCGAGAACGTCAAAGCAAAGATCCAAGACAAGGAAGGCATTCCTCC GTCGAGCCCAGTGACACTATCGAGAACGTCAAGGCAAAGATCCAAGACAAGGAAGGCATTCCTCC T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:124912956..124913225 26863196 MeRIP-seq:(Medium) rs116167503 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_35136,Human_RBP_ID_1467387,Human_RBP_ID_1790259,Human_RBP_ID_3397568,Human_RBP_ID_8369135,Human_RBP_ID_8787464,Human_RBP_ID_9255621,Human_RBP_ID_9279376,Human_RBP_ID_24543218,Human_RBP_ID_26413633,Human_RBP_ID_26807307,Human_RBP_ID_27807429 Human_miRNA_ID_1264451,Human_miRNA_ID_1269541,Human_miRNA_ID_1697215 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161585 116025 RMVar_ID_116025 Human_SNP_ID_815190618 m1A Human chr12 + 56158697 56158697 56158697 TTCCCTCTTCTCTGAGCAGTGTGACTTCACCGAAGACCAGACCGCAGGTAGGTTATCTCTGATCC TTCCCTCTTCTCTGAGCAGTGTGACTTCACCGTAGACCAGACCGCAGGTAGGTTATCTCTGATCC A T MYL6,MYL6B Ensembl:ENSG00000092841,Ensembl:ENSG00000196465 Protein coding,Protein coding CDS,exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56157971..56159753 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 13 liver Human_RBP_ID_753140,Human_RBP_ID_874683,Human_RBP_ID_1474263,Human_RBP_ID_4246746,Human_RBP_ID_5111757,Human_RBP_ID_5346698,Human_RBP_ID_17650738,Human_RBP_ID_19056353,Human_RBP_ID_22436504,Human_RBP_ID_22471999,Human_RBP_ID_22538701,Human_RBP_ID_22646528,Human_RBP_ID_22736913,Human_RBP_ID_22905981,Human_RBP_ID_23207691 Human_Splice_Rec_1381744,Human_Splice_Rec_1381745,Human_Splice_Rec_1381750,Human_Splice_Rec_1381751,Human_Splice_Rec_1381758,Human_Splice_Rec_1381768,Human_Splice_Rec_1381769,Human_Splice_Rec_1381776,Human_Splice_Rec_1381777,Human_Splice_Rec_1381786,Human_Splice_Rec_1381787,Human_Splice_Rec_1381798,Human_Splice_Rec_1381799,Human_Splice_Rec_1381808,Human_Splice_Rec_1381809,Human_Splice_Rec_1381813,Human_Splice_Rec_1381820,Human_Splice_Rec_1381821,Human_Splice_Rec_1381831,Human_Splice_Rec_1381838,Human_Splice_Rec_1381839,Human_Splice_Rec_1381848,Human_Splice_Rec_1381849,Human_Splice_Rec_1381854,Human_Splice_Rec_1381855,Human_Splice_Rec_1381866,Human_Splice_Rec_1381867,Human_Splice_Rec_1381874,Human_Splice_Rec_1381875,Human_Splice_Rec_1381881,Human_Splice_Rec_1381884,Human_Splice_Rec_1381885,Human_Splice_Rec_1381892,Human_Splice_Rec_1381893,Human_Splice_Rec_1381904,Human_Splice_Rec_1381905 RMVar_hsa_circ_84206,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224,RMVar_hsa_circ_112837,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_157227,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229 116026 RMVar_ID_116026 Human_SNP_ID_815190957 m1A Human chr12 + 13000248 13000248 13000248 GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAAGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG GGGCGGCAGGGCGGCAGGGTGGCAGGGCGGCAGGGCGGCGGGACGGCGAGGCGGCGAGGCGAGAG A G GPRC5D-AS1 RNACentral:URS0000BC43D8 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:13000149..13000275 26863410 MeRIP-seq:(Medium) rs1036063783 Functional Loss SNV ICGC 33..33 33 CHOL 1 - 116027 RMVar_ID_116027 Human_SNP_ID_815195879 m1A Human chr12 - 122871059 122871059 122871059 GGTTCTCATCATCTTGTGTGTTCCTTGCAGACACAGAATGTTCAGCTTAACAAAGAAATGACACT GGTTCTCATCATCTTGTGTGTTCCTTGCAGACCCAGAATGTTCAGCTTAACAAAGAAATGACACT T G AC027290.3,VPS37B Ensembl:ENSG00000280138,Ensembl:ENSG00000139722 Other,Protein coding exon,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:122870971..122871119;chr12:122871023..122871120 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_876011,Human_RBP_ID_22645548,Human_RBP_ID_24943776 Human_Splice_Rec_1438206,Human_Splice_Rec_1438218,Human_Splice_Rec_1438224 Human_miRNA_ID_3201905 RMVar_hsa_circ_37382 116028 RMVar_ID_116028 Human_SNP_ID_815195886 m1A Human chr12 - 122871059 122871059 122871059 GGTTCTCATCATCTTGTGTGTTCCTTGCAGACACAGAATGTTCAGCTTAACAAAGAAATGACACT GGTTCTCATCATCTTGTGTGTTCCTTGCAGACGCAGAATGTTCAGCTTAACAAAGAAATGACACT T C AC027290.3,VPS37B Ensembl:ENSG00000280138,Ensembl:ENSG00000139722 Other,Protein coding exon,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:122870971..122871119;chr12:122871023..122871120 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_876011,Human_RBP_ID_22645548,Human_RBP_ID_24943776 Human_Splice_Rec_1438206,Human_Splice_Rec_1438218,Human_Splice_Rec_1438224 Human_miRNA_ID_3201905 RMVar_hsa_circ_37382 116029 RMVar_ID_116029 Human_SNP_ID_815206341 m1A Human chr12 - 96247330 96247330 96247330 CGCCGCCGCAGCCTCTGACGTGGAAGGCAGGGACACCACCGGCCTGGTGACGTGCTTGTCGGTTT CGCCGCCGCAGCCTCTGACGTGGAAGGCAGGGGCACCACCGGCCTGGTGACGTGCTTGTCGGTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:96247282..96247729 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116030 RMVar_ID_116030 Human_SNP_ID_815213806 m1A Human chr12 - 42238165 42238165 42238165 GCGGTGATAGCCAAGCCATGGGAGACAAGAAGAGCCCCACCAGGTAACAGCGCCCGGGCCCCGGG GCGGTGATAGCCAAGCCATGGGAGACAAGAAGCGCCCCACCAGGTAACAGCGCCCGGGCCCCGGG T G YAF2 Ensembl:ENSG00000015153 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:42237888..42238197 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain Human_RBP_ID_229643,Human_RBP_ID_874397,Human_RBP_ID_4248115,Human_RBP_ID_18975464 Human_Splice_Rec_1356147,Human_Splice_Rec_1356155,Human_Splice_Rec_1356161,Human_Splice_Rec_1356165,Human_Splice_Rec_1356177,Human_Splice_Rec_1356189,Human_Splice_Rec_1356203,Human_Splice_Rec_1356211,Human_Splice_Rec_1356225,Human_Splice_Rec_1356237,Human_Splice_Rec_1356245,Human_Splice_Rec_1356249 116031 RMVar_ID_116031 Human_SNP_ID_815225961 m1A Human chr12 + 49273169 49273169 49273169 GGCCCGTGAGGACATGGCTGCCCTTGAGAAGGATTATGAGGAGGTTGGAGCAGATAGTGCTGACG GGCCCGTGAGGACATGGCTGCCCTTGAGAAGGGTTATGAGGAGGTTGGAGCAGATAGTGCTGACG A G TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:49273087..49273250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_420873,Human_RBP_ID_1472655,Human_RBP_ID_1796060,Human_RBP_ID_2339968,Human_RBP_ID_3406956,Human_RBP_ID_4225287,Human_RBP_ID_5111441,Human_RBP_ID_6190730,Human_RBP_ID_8377178,Human_RBP_ID_11954999,Human_RBP_ID_17186180,Human_RBP_ID_17650359,Human_RBP_ID_17830273,Human_RBP_ID_19703237,Human_RBP_ID_22437013,Human_RBP_ID_23561898,Human_RBP_ID_26423658 Human_miRNA_ID_1473728 RMVar_hsa_circ_118502,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156317,RMVar_hsa_circ_107279,RMVar_hsa_circ_83896,RMVar_hsa_circ_156318,RMVar_hsa_circ_156319 116032 RMVar_ID_116032 Human_SNP_ID_815227970 m1A Human chr12 - 57526988 57526988 57526988 GAAAGAGGCAAGGAGGTTGCTGGGAGGTGCTGAAGGAGGTGGAAGAAGGTCTGAGGGTGGTGGAG GAAAGAGGCAAGGAGGTTGCTGGGAGGTGCTGGAGGAGGTGGAAGAAGGTCTGAGGGTGGTGGAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57526939..57527026 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 116033 RMVar_ID_116033 Human_SNP_ID_815230603 m1A Human chr12 + 121827020 121827020 121827020 CGGAGCTTAGGATGGGGATCTCCGGCCCGGGGACCTAAGTGTAGGCATCGCCAGGAGAGAAGTGG CGGAGCTTAGGATGGGGATCTCCGGCCCGGGGGCCTAAGTGTAGGCATCGCCAGGAGAGAAGTGG A G SETD1B Ensembl:ENSG00000139718 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:121827008..121827420 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116034 RMVar_ID_116034 Human_SNP_ID_815257121 m1A Human chr12 - 54054253 54054253 54054253 GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGGACGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG GGCTGGCTGGCTGCAGGCTGGCGGGGCTGGGGGCGGGGAGGCGGAGGCGCCTGAGAGAGGCGCCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:54054204..54054353 26863196 MeRIP-seq:(Medium) rs967730434 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,oesophagus squamous_cell_carcinoma 3 oesophagus 116035 RMVar_ID_116035 Human_SNP_ID_815258100 m1A Human chr12 + 108731419 108731419 108731419 GACTCGCTCTCAGGCTGCCCCCGCCGGGCGCGAGCCGCTCACCCGGGCCGAGGTGCCTGAGGCGC GACTCGCTCTCAGGCTGCCCCCGCCGGGCGCGCGCCGCTCACCCGGGCCGAGGTGCCTGAGGCGC A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:108731402..108731500 26863410 MeRIP-seq:(Medium) rs11114043 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 1 brain GWAS_ID_6942,GWAS_ID_6943,GWAS_ID_6944,GWAS_ID_6945,GWAS_ID_6946,GWAS_ID_6947,GWAS_ID_6948,GWAS_ID_6949 116036 RMVar_ID_116036 Human_SNP_ID_815258703 m1A Human chr12 + 56160580 56160580 56160580 ATGTCTGTCCCCACTGCCTGACCCCTCACCCCATGTCTTTGTCTTGTCTTCACCATGAATGTCTC ATGTCTGTCCCCACTGCCTGACCCCTCACCCCGTGTCTTTGTCTTGTCTTCACCATGAATGTCTC A G MYL6 Ensembl:ENSG00000092841 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56160575..56160685 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 14 uterus Human_RBP_ID_3409228,Human_RBP_ID_5347476,Human_RBP_ID_19787800,Human_RBP_ID_21967907,Human_RBP_ID_24365616 Human_Splice_Rec_1381765,Human_Splice_Rec_1381795,Human_Splice_Rec_1381829,Human_Splice_Rec_1381901 RMVar_hsa_circ_84206,RMVar_hsa_circ_81881,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_157229,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235,RMVar_hsa_circ_126953,RMVar_hsa_circ_98857,RMVar_hsa_circ_157236,RMVar_hsa_circ_157237 116037 RMVar_ID_116037 Human_SNP_ID_815264457 m1A Human chr12 + 26979874 26979874 26979874 GAGCATGCAGATCGAGAGGATTCCAAATCGCCACCACACAGCTACCAAGAACATTCCACCGACGC GAGCATGCAGATCGAGAGGATTCCAAATCGCCGCCACACAGCTACCAAGAACATTCCACCGACGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:26979824..26979924 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 1 haematopoietic and lymphoid tissue 116038 RMVar_ID_116038 Human_SNP_ID_815275122 m1A Human chr12 + 2803200 2803200 2803200 CTCAGGAGACCATCCCACTGACACAGAGATGAAGGAGGAGCAGAAGAGCAACACGGCAGGGAGCC CTCAGGAGACCATCCCACTGACACAGAGATGAGGGAGGAGCAGAAGAGCAACACGGCAGGGAGCC A G FKBP4 Ensembl:ENSG00000004478 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:2803120..2803291 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6172320,Human_RBP_ID_9364515,Human_RBP_ID_11917344,Human_RBP_ID_23555182 Human_Splice_Rec_1324748,Human_Splice_Rec_1324765 116039 RMVar_ID_116039 Human_SNP_ID_815276341 m1A Human chr12 + 96036077 96036077 96036077 TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGATTCCCCGACGGGGAGGCACAGTAATTGTTTTT TCCCCGCCTGTCACGCGGGAGACCGGGGTTCGCTTCCCCGACGGGGAGGCACAGTAATTGTTTTT A C tRNA-Asp-GTC-2-1,NONHSAG011990.2,NONHSAG011990.2:2,AB330774-001,AB330774-001:2,TRD-GTC2-10 RNACentral:URS00006174C2,RNACentral:URS00008B3E1C,RNACentral:URS00009C253D,RNACentral:URS00000711F0,RNACentral:URS00002B094D,RNACentral:URS00005EA0AD tRNA,lincRNA,lincRNA,misc_RNA,misc_RNA,tRNA exon,intron,intron,exon,exon,exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_430687,Human_RBP_ID_1358935,Human_RBP_ID_1479151,Human_RBP_ID_1803529,Human_RBP_ID_6236623,Human_RBP_ID_8385853,Human_RBP_ID_9023900,Human_RBP_ID_17581824,Human_RBP_ID_17829538,Human_RBP_ID_18434910,Human_RBP_ID_18635225,Human_RBP_ID_19829548,Human_RBP_ID_22795594,Human_RBP_ID_23125981,Human_RBP_ID_23579945,Human_RBP_ID_26616474,Human_RBP_ID_27635285 116040 RMVar_ID_116040 Human_SNP_ID_815284774 m1A Human chr12 - 120496174 120496174 120496174 GGGGCTGGCCGACTGCAACGGTCTCCTGGGGGAGGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT GGGGCTGGCCGACTGCAACGGTCTCCTGGGGGGGGTGCTAGCACAGCTCAGGCCCGGCTAGAGAT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEK293T cell line,total RNA;HTR8/Svneo,Normoxia chr12:120496126..120496200;chr12:120496126..120496225 26863196,32194978 MeRIP-seq:(Medium) rs580016 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_12069,GWAS_ID_12070,GWAS_ID_12071,GWAS_ID_12072,GWAS_ID_12073,GWAS_ID_12074,GWAS_ID_12075,GWAS_ID_12076,GWAS_ID_12077,GWAS_ID_12078,GWAS_ID_12079,GWAS_ID_12080,GWAS_ID_12081,GWAS_ID_12082,GWAS_ID_12083,GWAS_ID_12084,GWAS_ID_12085,GWAS_ID_12086 116041 RMVar_ID_116041 Human_SNP_ID_815285575 m1A Human chr12 - 132782378 132782378 132782378 GAAAGGGAAGCTTACGGGCCTCGGTCAGTCCAACGCAGCTCTGCGGGAACACAACAGCATCCTAG GAAAGGGAAGCTTACGGGCCTCGGTCAGTCCAGCGCAGCTCTGCGGGAACACAACAGCATCCTAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132782268..132782433 26863196 MeRIP-seq:(Medium) rs765767645 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_876354,Human_RBP_ID_3398895,Human_RBP_ID_9365963,Human_RBP_ID_18622722 Human_Splice_Rec_1447231,Human_Splice_Rec_1447277,Human_Splice_Rec_1447329 Human_miRNA_ID_1980898,Human_miRNA_ID_1982622 RMVar_hsa_circ_3416,RMVar_hsa_circ_82224,RMVar_hsa_circ_161878,RMVar_hsa_circ_340011,RMVar_hsa_circ_161881,RMVar_hsa_circ_161879,RMVar_hsa_circ_118136,RMVar_hsa_circ_368835,RMVar_hsa_circ_81837,RMVar_hsa_circ_103681,RMVar_hsa_circ_268395,RMVar_hsa_circ_294782,RMVar_hsa_circ_316454,RMVar_hsa_circ_60268,RMVar_hsa_circ_75106,RMVar_hsa_circ_161882,RMVar_hsa_circ_161883,RMVar_hsa_circ_161884,RMVar_hsa_circ_302166,RMVar_hsa_circ_374528,RMVar_hsa_circ_84355,RMVar_hsa_circ_161886,RMVar_hsa_circ_33931,RMVar_hsa_circ_161887,RMVar_hsa_circ_161885 116042 RMVar_ID_116042 Human_SNP_ID_815293596 m1A Human chr12 + 55990800 55990800 55990800 AGCTGACCTGGCCAACAAACGTATGGTGGAGTATGAAGTAAGGTGGCCCGTGGAGTTCCTCTCTA AGCTGACCTGGCCAACAAACGTATGGTGGAGTGTGAAGTAAGGTGGCCCGTGGAGTTCCTCTCTA A G RAB5B Ensembl:ENSG00000111540 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:55990676..55990825 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_23566368 Human_Splice_Rec_1380717,Human_Splice_Rec_1380725,Human_Splice_Rec_1380739,Human_Splice_Rec_1380775,Human_Splice_Rec_1380781 Human_miRNA_ID_1391675,Human_miRNA_ID_1699526 RMVar_hsa_circ_2346,RMVar_hsa_circ_309699,RMVar_hsa_circ_157135 116043 RMVar_ID_116043 Human_SNP_ID_815301305 m1A Human chr12 - 6975252 6975252 6975252 GTGCCAACTTTCATACATCCAACTGGAAAGTGATCTGATACTGGATTCTTAATTACCTAAAGTAA GTGCCAACTTTCATACATCCAACTGGAAAGTGTTCTGATACTGGATTCTTAATTACCTAAAGTAA T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6975121..6975301 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 116044 RMVar_ID_116044 Human_SNP_ID_815322598 m1A Human chr12 - 53715844 53715844 53715844 AGGCTGGCTGAGCTCGGTTTGCACTTGAAGGAAGAAAAATGCCAATGGAGCAAGGAGCGGGCAGG AGGCTGGCTGAGCTCGGTTTGCACTTGAAGGAGGAAAAATGCCAATGGAGCAAGGAGCGGGCAGG T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53715775..53716003 26863196 MeRIP-seq:(Medium) rs1175977607 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_18977244 Human_Splice_Rec_1376359,Human_Splice_Rec_1376387,Human_Splice_Rec_1376423,Human_Splice_Rec_1376451,Human_Splice_Rec_1376477,Human_Splice_Rec_1376485 116045 RMVar_ID_116045 Human_SNP_ID_815349161 m1A Human chr12 + 112022575 112022573 112022576 GGCTGATTGAGAAGAACAAGATGAGTGACGGGAAGAAGGAGGAGCTCCAGAAGAGCTTAAACATC GGCTGATTGAGAAGAACAAGATGAGTGACGG___GAAGGAGGAGCTCCAGAAGAGCTTAAACATC GGAA G ERP29 Ensembl:ENSG00000089248 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:112022158..112022975 26863196 MeRIP-seq:(Medium) rs1352097022 Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_410964,Human_RBP_ID_1464700,Human_RBP_ID_3393502,Human_RBP_ID_4201361,Human_RBP_ID_6133798,Human_RBP_ID_11817377,Human_RBP_ID_22757366,Human_RBP_ID_23538541,Human_RBP_ID_26321018,Human_RBP_ID_26421629 116046 RMVar_ID_116046 Human_SNP_ID_815352424 m1A Human chr12 + 49272509 49272500 49272509 TGCCTTCATGGTAGACAATGAGGCCATCTATGACATCTGTCGTAGAAACCTCGATATCGAGCGCC TGCCTTCATGGTAGACAATGAGGC_________CATCTGTCGTAGAAACCTCGATATCGAGCGCC CCATCTATGA C TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 25..33 33 BRCA 1 - Human_miRNA_ID_2534634,Human_miRNA_ID_2536366 RMVar_hsa_circ_118502,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156317,RMVar_hsa_circ_107279,RMVar_hsa_circ_83896,RMVar_hsa_circ_156318,RMVar_hsa_circ_156319 116047 RMVar_ID_116047 Human_SNP_ID_815356419 m1A Human chr12 - 122522296 122522296 122522296 ACTTTAATCATTTGTTTTTAAACTTTTAGGCTAGTGATACAGAGCGAGATGGACTAGCCCCAGAA ACTTTAATCATTTGTTTTTAAACTTTTAGGCTGGTGATACAGAGCGAGATGGACTAGCCCCAGAA T C RSRC2 Ensembl:ENSG00000111011 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:122522251..122522300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_24942412 Human_Splice_Rec_1437358,Human_Splice_Rec_1437376,Human_Splice_Rec_1437396,Human_Splice_Rec_1437416,Human_Splice_Rec_1437446,Human_Splice_Rec_1437488,Human_Splice_Rec_1437504,Human_Splice_Rec_1437520,Human_Splice_Rec_1437542,Human_Splice_Rec_1437552 RMVar_hsa_circ_54145,RMVar_hsa_circ_72827,RMVar_hsa_circ_356319,RMVar_hsa_circ_330603,RMVar_hsa_circ_161085,RMVar_hsa_circ_34303,RMVar_hsa_circ_74106,RMVar_hsa_circ_350093 116048 RMVar_ID_116048 Human_SNP_ID_815366788 m1A Human chr12 + 6864100 6864100 6864100 TCCTGCCTGGCTCTAGTGGGCCGGGCTCCACAAGCGCAGCAGCCGACCCCCCTCCTGAGGACTGT TCCTGCCTGGCTCTAGTGGGCCGGGCTCCACACGCGCAGCAGCCGACCCCCCTCCTGAGGACTGT A C USP5 Ensembl:ENSG00000111667 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6863976..6864112 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_22436852 Human_Splice_Rec_1332642,Human_Splice_Rec_1332643,Human_Splice_Rec_1332680,Human_Splice_Rec_1332681,Human_Splice_Rec_1332718,Human_Splice_Rec_1332719,Human_Splice_Rec_1332737 RMVar_hsa_circ_122697,RMVar_hsa_circ_154633,RMVar_hsa_circ_102387,RMVar_hsa_circ_154635,RMVar_hsa_circ_90267,RMVar_hsa_circ_154636,RMVar_hsa_circ_104134,RMVar_hsa_circ_88840,RMVar_hsa_circ_122307,RMVar_hsa_circ_154638,RMVar_hsa_circ_334059,RMVar_hsa_circ_154639,RMVar_hsa_circ_154640,RMVar_hsa_circ_114334,RMVar_hsa_circ_154643,RMVar_hsa_circ_326111,RMVar_hsa_circ_154644,RMVar_hsa_circ_154645 116049 RMVar_ID_116049 Human_SNP_ID_815381108 m1A Human chr12 + 109052727 109052727 109052727 CCGAGGCGGCGATGACCGCGGCCGACAGGGCCATCCAGCGCTTCCTGCGGACCGGGGCGGCCGTC CCGAGGCGGCGATGACCGCGGCCGACAGGGCCTTCCAGCGCTTCCTGCGGACCGGGGCGGCCGTC A T USP30 Ensembl:ENSG00000135093 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:109052676..109053718 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_4246957 Human_Splice_Rec_1420355,Human_Splice_Rec_1420379,Human_Splice_Rec_1420391,Human_Splice_Rec_1420407 RMVar_hsa_circ_77775,RMVar_hsa_circ_159667 116050 RMVar_ID_116050 Human_SNP_ID_815390432 m1A Human chr12 + 10213113 10213113 10213113 CGAAGGAGGCAGGCCCCGCGCGGGGATCTCGGAAGCCCTGCGGTGCATCATGAAGTTCCAGTACA CGAAGGAGGCAGGCCCCGCGCGGGGATCTCGGTAGCCCTGCGGTGCATCATGAAGTTCCAGTACA A T GABARAPL1 Ensembl:ENSG00000139112 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:10212907..10213200;chr12:10212907..10213206;chr12:10212901..10213200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_miRNA_ID_1272939 116051 RMVar_ID_116051 Human_SNP_ID_815407455 m1A Human chr12 - 76056120 76056119 76056120 AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAAGATGAAGAAAAAGAAGACCCCAAAGGAATTCC AAAGAAAAGGCCAAGATTGAAGATGAGAAAAA_GATGAAGAAAAAGAAGACCCCAAAGGAATTCC CT C NAP1L1 Ensembl:ENSG00000187109 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_194442,Human_RBP_ID_811191,Human_RBP_ID_877958,Human_RBP_ID_1477980,Human_RBP_ID_1801678,Human_RBP_ID_2368915,Human_RBP_ID_4241894,Human_RBP_ID_6222062,Human_RBP_ID_8247862,Human_RBP_ID_8383957,Human_RBP_ID_9365251,Human_RBP_ID_17240742,Human_RBP_ID_17473808,Human_RBP_ID_18410892,Human_RBP_ID_18526788,Human_RBP_ID_18633610,Human_RBP_ID_22001529,Human_RBP_ID_22909227,Human_RBP_ID_23113344,Human_RBP_ID_23574917,Human_RBP_ID_24543107,Human_RBP_ID_25003582,Human_RBP_ID_26320975,Human_RBP_ID_26911848,Human_RBP_ID_27805738 Human_Splice_Rec_1400534,Human_Splice_Rec_1400535,Human_Splice_Rec_1400562,Human_Splice_Rec_1400563,Human_Splice_Rec_1400588,Human_Splice_Rec_1400589,Human_Splice_Rec_1400618,Human_Splice_Rec_1400619,Human_Splice_Rec_1400644,Human_Splice_Rec_1400645,Human_Splice_Rec_1400666,Human_Splice_Rec_1400667,Human_Splice_Rec_1400690,Human_Splice_Rec_1400691,Human_Splice_Rec_1400716,Human_Splice_Rec_1400717,Human_Splice_Rec_1400742,Human_Splice_Rec_1400743,Human_Splice_Rec_1400770,Human_Splice_Rec_1400771,Human_Splice_Rec_1400796,Human_Splice_Rec_1400797,Human_Splice_Rec_1400809,Human_Splice_Rec_1400840,Human_Splice_Rec_1400841,Human_Splice_Rec_1400858,Human_Splice_Rec_1400859,Human_Splice_Rec_1400878,Human_Splice_Rec_1400879,Human_Splice_Rec_1400900,Human_Splice_Rec_1400901,Human_Splice_Rec_1400918,Human_Splice_Rec_1400919,Human_Splice_Rec_1400932,Human_Splice_Rec_1400933,Human_Splice_Rec_1400948,Human_Splice_Rec_1400949,Human_Splice_Rec_1400962,Human_Splice_Rec_1400963,Human_Splice_Rec_1400970 Human_miRNA_ID_2157685,Human_miRNA_ID_2157686 RMVar_hsa_circ_1721,RMVar_hsa_circ_84271,RMVar_hsa_circ_158351,RMVar_hsa_circ_125050,RMVar_hsa_circ_352895,RMVar_hsa_circ_339462,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158355,RMVar_hsa_circ_158356,RMVar_hsa_circ_83129,RMVar_hsa_circ_41971,RMVar_hsa_circ_158358,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_40655,RMVar_hsa_circ_158361,RMVar_hsa_circ_303154,RMVar_hsa_circ_309215,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_367606 116052 RMVar_ID_116052 Human_SNP_ID_815426959 m1A Human chr12 + 50200856 50200856 50200856 CATTCTCCTTTTGCTCCATTTTATGAATTTTGATTTCGCCACCACTGGCTTTCAGCTCATTCTAC CATTCTCCTTTTGCTCCATTTTATGAATTTTGGTTTCGCCACCACTGGCTTTCAGCTCATTCTAC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:50195821..50200940 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 8 head and neck 116053 RMVar_ID_116053 Human_SNP_ID_815446934 m1A Human chr12 - 991324 991324 991324 TTCCGCGCTGTCGCCGCCGCCGCGGCCGTCTCACCGTCCTCAGGGCTGCCGCTACTGCTGCTGCT TTCCGCGCTGTCGCCGCCGCCGCGGCCGTCTCTCCGTCCTCAGGGCTGCCGCTACTGCTGCTGCT T A - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:991273..991425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 116054 RMVar_ID_116054 Human_SNP_ID_815453042 m1A Human chr12 + 57091906 57091906 57091906 TTGGGCACATCTTTGAGATGGATGATAATGACAGCCAGAAGGAAGAGGAGATCCGCAAATACAGC TTGGGCACATCTTTGAGATGGATGATAATGACGGCCAGAAGGAAGAGGAGATCCGCAAATACAGC A G NAB2 Ensembl:ENSG00000166886 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57091858..57091929 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_9365117 Human_Splice_Rec_1386063,Human_Splice_Rec_1386073 116055 RMVar_ID_116055 Human_SNP_ID_815484152 m1A Human chr12 + 56601672 56601672 56601672 GCTGAGATGTTAAACCAGAGTGCTTGAGGATCAGGGCTGGATTCTGCCTCATCAGGCTCTGGCTC GCTGAGATGTTAAACCAGAGTGCTTGAGGATCGGGGCTGGATTCTGCCTCATCAGGCTCTGGCTC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56601651..56601675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_18629942 116056 RMVar_ID_116056 Human_SNP_ID_815505105 m1A Human chr12 + 12851202 12851202 12851202 GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCACCTGCTACTGAGTAAGGGGCATTCCTGTTACA GAAGCAGGGTGTCTTGACCCATGGCCGTGTCCGCCTGCTACTGAGTAAGGGGCATTCCTGTTACA A G AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs3825274 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_9013270 116057 RMVar_ID_116057 Human_SNP_ID_815513225 m1A Human chr12 - 55725883 55725880 55725883 TTGTGCCTGCCACCTTCAGGGCTGTGTGGAGAAGATTGGGGGCTGGCTGAGGAAAAATGTGCTGG TTGTGCCTGCCACCTTCAGGGCTGTGTGGAGA___TTGGGGGCTGGCTGAGGAAAAATGTGCTGG ATCT A CD63 Ensembl:ENSG00000135404 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:55725789..55725942 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 COAD 1 - Human_RBP_ID_3319,Human_RBP_ID_34764,Human_RBP_ID_228946,Human_RBP_ID_753667,Human_RBP_ID_876216,Human_RBP_ID_5111471,Human_RBP_ID_5314953,Human_RBP_ID_5346656,Human_RBP_ID_6199138,Human_RBP_ID_9344541,Human_RBP_ID_17650139,Human_RBP_ID_17684838,Human_RBP_ID_17830885,Human_RBP_ID_22436469,Human_RBP_ID_22644927,Human_RBP_ID_22755961,Human_RBP_ID_23125696,Human_RBP_ID_23207677,Human_RBP_ID_23566070 Human_Splice_Rec_1379088,Human_Splice_Rec_1379089,Human_Splice_Rec_1379102,Human_Splice_Rec_1379103,Human_Splice_Rec_1379106,Human_Splice_Rec_1379107,Human_Splice_Rec_1379114,Human_Splice_Rec_1379115,Human_Splice_Rec_1379122,Human_Splice_Rec_1379123,Human_Splice_Rec_1379134,Human_Splice_Rec_1379135,Human_Splice_Rec_1379146,Human_Splice_Rec_1379147,Human_Splice_Rec_1379160,Human_Splice_Rec_1379161,Human_Splice_Rec_1379174,Human_Splice_Rec_1379175,Human_Splice_Rec_1379186,Human_Splice_Rec_1379187,Human_Splice_Rec_1379198,Human_Splice_Rec_1379199,Human_Splice_Rec_1379210,Human_Splice_Rec_1379211,Human_Splice_Rec_1379213,Human_Splice_Rec_1379226,Human_Splice_Rec_1379238 Human_miRNA_ID_2397858,Human_miRNA_ID_2397859 RMVar_hsa_circ_90672,RMVar_hsa_circ_100926,RMVar_hsa_circ_157113,RMVar_hsa_circ_55281,RMVar_hsa_circ_157115 116058 RMVar_ID_116058 Human_SNP_ID_815517242 m1A Human chr12 - 48153487 48153487 48153487 GCATGTGAACACCTTGAGCCTTGATGAGTTCCAGTATGTGGTATATTATGCAGAGCATTCAGAGC GCATGTGAACACCTTGAGCCTTGATGAGTTCCGGTATGTGGTATATTATGCAGAGCATTCAGAGC T C ASB8 Ensembl:ENSG00000177981 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48153436..48153511 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 9 large intestine Human_RBP_ID_1472135,Human_RBP_ID_1795653,Human_RBP_ID_3406585,Human_RBP_ID_11950395 Human_Splice_Rec_1362118,Human_Splice_Rec_1362124,Human_Splice_Rec_1362134,Human_Splice_Rec_1362142,Human_Splice_Rec_1362148,Human_Splice_Rec_1362156,Human_Splice_Rec_1362164,Human_Splice_Rec_1362174,Human_Splice_Rec_1362180,Human_Splice_Rec_1362190,Human_Splice_Rec_1362198,Human_Splice_Rec_1362204,Human_Splice_Rec_1362212,Human_Splice_Rec_1362216,Human_Splice_Rec_1362222 RMVar_hsa_circ_1020,RMVar_hsa_circ_30855,RMVar_hsa_circ_72518,RMVar_hsa_circ_86553,RMVar_hsa_circ_358749,RMVar_hsa_circ_156182 116059 RMVar_ID_116059 Human_SNP_ID_815545386 m1A Human chr12 - 65170466 65170466 65170466 GATTTAGCAGTCAGCGGGGGGAGAGGCTTACTATGGGTTCGTCTGGGCCGATGCCGGGAAAGGGA GATTTAGCAGTCAGCGGGGGGAGAGGCTTACTGTGGGTTCGTCTGGGCCGATGCCGGGAAAGGGA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:65170364..65170465 32194978 MeRIP-seq:(Medium) rs147328826 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116060 RMVar_ID_116060 Human_SNP_ID_815550764 m1A Human chr12 - 108562690 108562690 108562690 GTCGGGCCGGGGCCGACAGCTCCCGGGCGGGCAGGCGGGGGCTCCGCAGCAGCAGAGCCGATGCC GTCGGGCCGGGGCCGACAGCTCCCGGGCGGGCCGGCGGGGGCTCCGCAGCAGCAGAGCCGATGCC T G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:108562644..108562791 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 6 oesophagus 116061 RMVar_ID_116061 Human_SNP_ID_815576841 m1A Human chr12 + 56285967 56285967 56285967 CCCACCACCGTCTTGCCATGTTGCTGCCTGAAAGTCTTAATTCTGGCCTGCTCCTTAGGTATCAG CCCACCACCGTCTTGCCATGTTGCTGCCTGAAGGTCTTAATTCTGGCCTGCTCCTTAGGTATCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56285897..56286007 26863196 MeRIP-seq:(Medium) rs1802236 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Clinvar_Rec_514 GWAS_ID_11700,GWAS_ID_11701,GWAS_ID_11702,GWAS_ID_11703,GWAS_ID_11704,GWAS_ID_11705,GWAS_ID_11706,GWAS_ID_11707,GWAS_ID_11708,GWAS_ID_11709,GWAS_ID_11710,GWAS_ID_11711,GWAS_ID_11712,GWAS_ID_11713,GWAS_ID_11714,GWAS_ID_11715,GWAS_ID_11716,GWAS_ID_11717,GWAS_ID_11718,GWAS_ID_11719,GWAS_ID_11720,GWAS_ID_11721,GWAS_ID_11722,GWAS_ID_11723,GWAS_ID_11724,GWAS_ID_11725,GWAS_ID_11726,GWAS_ID_11727,GWAS_ID_11728,GWAS_ID_11729,GWAS_ID_11730,GWAS_ID_11731,GWAS_ID_11732,GWAS_ID_11733,GWAS_ID_11734,GWAS_ID_11735,GWAS_ID_11736,GWAS_ID_11737,GWAS_ID_11738,GWAS_ID_11739,GWAS_ID_11740,GWAS_ID_11741,GWAS_ID_11742,GWAS_ID_11743,GWAS_ID_11744,GWAS_ID_11745,GWAS_ID_11746,GWAS_ID_11747,GWAS_ID_11748,GWAS_ID_11749,GWAS_ID_11750,GWAS_ID_11751,GWAS_ID_11752,GWAS_ID_11753,GWAS_ID_11754,GWAS_ID_11755,GWAS_ID_11756,GWAS_ID_11757,GWAS_ID_11758,GWAS_ID_11759,GWAS_ID_11760,GWAS_ID_11761,GWAS_ID_11762,GWAS_ID_11763,GWAS_ID_11764,GWAS_ID_11765,GWAS_ID_11766,GWAS_ID_11767,GWAS_ID_11768,GWAS_ID_11769,GWAS_ID_11770,GWAS_ID_11771,GWAS_ID_11772,GWAS_ID_11773,GWAS_ID_11774,GWAS_ID_11775,GWAS_ID_11776,GWAS_ID_11777,GWAS_ID_11778,GWAS_ID_11779,GWAS_ID_11780,GWAS_ID_11781,GWAS_ID_11782,GWAS_ID_11783,GWAS_ID_11784,GWAS_ID_11785,GWAS_ID_11786,GWAS_ID_11787,GWAS_ID_11788,GWAS_ID_11789,GWAS_ID_11790,GWAS_ID_11791,GWAS_ID_11792,GWAS_ID_11793,GWAS_ID_11794,GWAS_ID_11795,GWAS_ID_11796,GWAS_ID_11797,GWAS_ID_11798,GWAS_ID_11799,GWAS_ID_11800,GWAS_ID_11801,GWAS_ID_11802,GWAS_ID_11803,GWAS_ID_11804,GWAS_ID_11805,GWAS_ID_11806,GWAS_ID_11807,GWAS_ID_11808,GWAS_ID_11809,GWAS_ID_11810,GWAS_ID_11811,GWAS_ID_11812 116062 RMVar_ID_116062 Human_SNP_ID_815596584 m1A Human chr12 + 122225996 122225996 122225996 CCTGAAGAATGAAGTTACGCTGCGCGACAGCCAACTCTTCAGAGCCGCCATTGTGCAGCGCGCGG CCTGAAGAATGAAGTTACGCTGCGCGACAGCCTACTCTTCAGAGCCGCCATTGTGCAGCGCGCGG A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122225857..122226000 26863196 MeRIP-seq:(Medium) rs139511903 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 6 lung 116063 RMVar_ID_116063 Human_SNP_ID_815598754 m1A Human chr12 - 124402452 124402450 124402453 AGATGAGAAGGAGAAGGAAAAGGAGGCGGAGAAGGAGGAGGAGAAGCCGGAGGTGGAGAACGACA AGATGAGAAGGAGAAGGAAAAGGAGGCGGAG___GAGGAGGAGAAGCCGGAGGTGGAGAACGACA CCTT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:124402351..124402610 26863196 MeRIP-seq:(Medium) rs1418191685 Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_35970,Human_RBP_ID_875407,Human_RBP_ID_3943838,Human_RBP_ID_9279360,Human_RBP_ID_18976454,Human_RBP_ID_24543214,Human_RBP_ID_26322341,Human_RBP_ID_27806236 Human_Splice_Rec_1441317,Human_Splice_Rec_1441411,Human_Splice_Rec_1441479,Human_Splice_Rec_1441547,Human_Splice_Rec_1441641,Human_Splice_Rec_1441785 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_161525,RMVar_hsa_circ_34554,RMVar_hsa_circ_99896,RMVar_hsa_circ_55111,RMVar_hsa_circ_359115,RMVar_hsa_circ_21997,RMVar_hsa_circ_123262,RMVar_hsa_circ_161521,RMVar_hsa_circ_333303,RMVar_hsa_circ_42196,RMVar_hsa_circ_356650,RMVar_hsa_circ_161522,RMVar_hsa_circ_161523,RMVar_hsa_circ_361562,RMVar_hsa_circ_376528,RMVar_hsa_circ_121865,RMVar_hsa_circ_303521,RMVar_hsa_circ_52164,RMVar_hsa_circ_161526,RMVar_hsa_circ_56917,RMVar_hsa_circ_161524 116064 RMVar_ID_116064 Human_SNP_ID_815604670 m1A Human chr12 - 113823288 113823288 113823288 GCCCCCGAAGAAAAAGCGGTCTGTGGTGTTGGACGAGATCCTGGAGCAGCTGGAAGGCAGTGACA GCCCCCGAAGAAAAAGCGGTCTGTGGTGTTGGGCGAGATCCTGGAGCAGCTGGAAGGCAGTGACA T C RBM19 Ensembl:ENSG00000122965 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:113823056..113823289 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - Human_RBP_ID_1356146,Human_RBP_ID_1787847,Human_RBP_ID_6137212,Human_RBP_ID_9365608,Human_RBP_ID_11828437,Human_RBP_ID_18977871,Human_RBP_ID_23539782 Human_Splice_Rec_1429262,Human_Splice_Rec_1429263,Human_Splice_Rec_1429310,Human_Splice_Rec_1429311,Human_Splice_Rec_1429358,Human_Splice_Rec_1429362 RMVar_hsa_circ_160390,RMVar_hsa_circ_93935,RMVar_hsa_circ_106154,RMVar_hsa_circ_116265,RMVar_hsa_circ_121814,RMVar_hsa_circ_160388,RMVar_hsa_circ_77868,RMVar_hsa_circ_87612,RMVar_hsa_circ_160392,RMVar_hsa_circ_160393,RMVar_hsa_circ_160394,RMVar_hsa_circ_160391,RMVar_hsa_circ_88809,RMVar_hsa_circ_160395 116065 RMVar_ID_116065 Human_SNP_ID_815633620 m1A Human chr12 - 6940931 6940931 6940931 GGAGAGTTCCAGCTGGGTAGGGGATCCGGGTAAGGTGAGACCCTGAGGCCAGGGGGTCAATGAGA GGAGAGTTCCAGCTGGGTAGGGGATCCGGGTAGGGTGAGACCCTGAGGCCAGGGGGTCAATGAGA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:6940876..6941025;chr12:6940862..6941025;chr12:6940876..6940977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 116066 RMVar_ID_116066 Human_SNP_ID_815638751 m1A Human chr12 + 56157516 56157516 56157516 GGAGGAGGTGGAGACCGTTCTGGCAGGACACGAGGACAGCAACGGCTGCATCAACTACGAGGGTG GGAGGAGGTGGAGACCGTTCTGGCAGGACACGCGGACAGCAACGGCTGCATCAACTACGAGGGTG A C MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56157359..56157580 26863196 MeRIP-seq:(Medium) rs1220331891 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate Human_RBP_ID_423659,Human_RBP_ID_810815,Human_RBP_ID_876937,Human_RBP_ID_5111979,Human_RBP_ID_5555496,Human_RBP_ID_17684895 Human_Splice_Rec_1381678,Human_Splice_Rec_1381679,Human_Splice_Rec_1381690,Human_Splice_Rec_1381691,Human_Splice_Rec_1381713,Human_Splice_Rec_1381730,Human_Splice_Rec_1381731,Human_Splice_Rec_1381735,Human_Splice_Rec_1381737,Human_Splice_Rec_1381741 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224 116067 RMVar_ID_116067 Human_SNP_ID_815649007 m1A Human chr12 - 53295611 53295611 53295611 CCACCTGGTCCAGCTGGTTCTTGAGCATTTCTAGCTGCGGCAGATTCAGCTCCGTGATGTTAATA CCACCTGGTCCAGCTGGTTCTTGAGCATTTCTGGCTGCGGCAGATTCAGCTCCGTGATGTTAATA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53295560..53295688 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate 116068 RMVar_ID_116068 Human_SNP_ID_815651874 m1A Human chr12 + 9312519 9312519 9312519 TCACCTGGACCCCTGCTGCTGGCATTGGCCACAAAGCCTCCTGGTCTGGCTCCAAAGCCTGGCAG TCACCTGGACCCCTGCTGCTGGCATTGGCCACGAAGCCTCCTGGTCTGGCTCCAAAGCCTGGCAG A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12831770 Functional Loss SNV ICGC 33..33 33 COCA 1 - 116069 RMVar_ID_116069 Human_SNP_ID_815671418 m1A Human chr12 - 48941052 48941052 48941052 CTTTGGAAACCTTCTCAAGAGCCTGATTGGGAAGAAGGAGATGCGCATCCTGATGGTGGGCCTGG CTTTGGAAACCTTCTCAAGAGCCTGATTGGGATGAAGGAGATGCGCATCCTGATGGTGGGCCTGG T A ARF3,AC073610.2 Ensembl:ENSG00000134287,Ensembl:ENSG00000272822 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:48941001..48941150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_1166935,Human_RBP_ID_1472395,Human_RBP_ID_1795874,Human_RBP_ID_4255279,Human_RBP_ID_26906790 RMVar_hsa_circ_97456,RMVar_hsa_circ_81388,RMVar_hsa_circ_156237,RMVar_hsa_circ_156241,RMVar_hsa_circ_156236,RMVar_hsa_circ_156243,RMVar_hsa_circ_271325,RMVar_hsa_circ_156244 116070 RMVar_ID_116070 Human_SNP_ID_815683225 m1A Human chr12 - 56131532 56131532 56131532 GGCGTCGGATGAAGAACATTGACACAGCCCCCACGAAGGGAAGGTCCCCAATGAGTGGCTCCAGT GGCGTCGGATGAAGAACATTGACACAGCCCCCCCGAAGGGAAGGTCCCCAATGAGTGGCTCCAGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56131476..56131575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 2 lung 116071 RMVar_ID_116071 Human_SNP_ID_815697065 m1A Human chr12 + 52904891 52904891 52904891 CACTCGGGAGAAGCTCGAGGAGCTGATGCGGGAACCGGGCCCACTCGTGTAGGAGCGGCTGCTGA CACTCGGGAGAAGCTCGAGGAGCTGATGCGGGCACCGGGCCCACTCGTGTAGGAGCGGCTGCTGA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:52904705..52905075 26863196 MeRIP-seq:(Medium) rs771489011 Functional Loss SNV ICGC,COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,colon adenocarcinoma,pancreas ductal_carcinoma,lung adenocarcinoma,oesophagus squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue angioimmunoblastic_T_cell_lymphoma,liver neoplasm,brain astrocytoma_Grade_IV,pancreas acinar_carcinoma,ovary serous_carcinoma,endometrium endometrioid_carcinoma,liver hepatocellular_carcinoma,colon tubulovillous,prostate adenocarcinoma,THCA,arm Merkel_cell_carcinoma,lung mixed_adenosquamous_carcinoma,large_intestine tubulovillous,lymph_node angioimmunoblastic_T_cell_lymphoma,kidney papillary_renal_cell_carcinoma,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,skin Merkel_cell_carcinoma 136 liver,skin,brain,lung,kidney,ovary,uterus,pancreas,oesophagus,prostate,large intestine,haematopoietic and lymphoid tissue,upper extremity 116072 RMVar_ID_116072 Human_SNP_ID_815703997 m1A Human chr12 - 120534715 120534715 120534715 GGCGTTCAGGGCCGGCGGGGGTCGGCGGCGGCAGCGGTTCTCGGCCTTCATGGCGACATTTTTCC GGCGTTCAGGGCCGGCGGGGGTCGGCGGCGGCTGCGGTTCTCGGCCTTCATGGCGACATTTTTCC T A - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:120534351..120534975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116073 RMVar_ID_116073 Human_SNP_ID_815717495 m1A Human chr12 - 56007893 56007893 56007893 GCCTCGGGCCAAACTCCCCCGGCCATCTTCCAACCCTCCGGCCCCAGCCCAACCCGCGACCCTCT GCCTCGGGCCAAACTCCCCCGGCCATCTTCCACCCCTCCGGCCCCAGCCCAACCCGCGACCCTCT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56007845..56008296 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116074 RMVar_ID_116074 Human_SNP_ID_815724390 m1A Human chr12 - 56724506 56724506 56724506 ATTCCCTTCCTTCAGAAATGCCCGGCGAAGCCACAGAAACCGTCCCTGCTACAGAGCAGGAGTTG ATTCCCTTCCTTCAGAAATGCCCGGCGAAGCCGCAGAAACCGTCCCTGCTACAGAGCAGGAGTTG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56724426..56724556 26863196 MeRIP-seq:(Medium) rs1361647025 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 9 uterus Human_RBP_ID_424372,Human_RBP_ID_754511,Human_RBP_ID_810687,Human_RBP_ID_876443,Human_RBP_ID_1474786,Human_RBP_ID_4257762,Human_RBP_ID_8380386,Human_RBP_ID_9365110,Human_RBP_ID_17241824,Human_RBP_ID_17357234,Human_RBP_ID_17475049,Human_RBP_ID_22437202,Human_RBP_ID_22794874,Human_RBP_ID_26323040,Human_RBP_ID_26909603 Human_Splice_Rec_1385288,Human_Splice_Rec_1385289,Human_Splice_Rec_1385308,Human_Splice_Rec_1385309,Human_Splice_Rec_1385324,Human_Splice_Rec_1385325,Human_Splice_Rec_1385340,Human_Splice_Rec_1385341,Human_Splice_Rec_1385354,Human_Splice_Rec_1385355,Human_Splice_Rec_1385368,Human_Splice_Rec_1385369,Human_Splice_Rec_1385386,Human_Splice_Rec_1385387,Human_Splice_Rec_1385400,Human_Splice_Rec_1385401,Human_Splice_Rec_1385414,Human_Splice_Rec_1385415,Human_Splice_Rec_1385426,Human_Splice_Rec_1385427,Human_Splice_Rec_1385438,Human_Splice_Rec_1385439,Human_Splice_Rec_1385446,Human_Splice_Rec_1385447,Human_Splice_Rec_1385456,Human_Splice_Rec_1385457,Human_Splice_Rec_1385468,Human_Splice_Rec_1385469,Human_Splice_Rec_1385476,Human_Splice_Rec_1385477,Human_Splice_Rec_1385482,Human_Splice_Rec_1385483,Human_Splice_Rec_1385488,Human_Splice_Rec_1385489,Human_Splice_Rec_1385494,Human_Splice_Rec_1385504,Human_Splice_Rec_1385505 Human_miRNA_ID_1767495 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_374757 116075 RMVar_ID_116075 Human_SNP_ID_815726930 m1A Human chr12 + 6329583 6329583 6329583 GCCGCACGAATTCCTTCCAGCGCAACGGGGGCACGTTCTCCACCACGGCGTACAGCGTCGCGGGG GCCGCACGAATTCCTTCCAGCGCAACGGGGGCGCGTTCTCCACCACGGCGTACAGCGTCGCGGGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6329416..6329638 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus 116076 RMVar_ID_116076 Human_SNP_ID_815729640 m1A Human chr12 - 53097834 53097834 53097834 CCATCCTCCTCCTCCACGCAGCCCCCTGGACAACCCGCCTGCACCCCTTGCCCGCAGCCTGGGCA CCATCCTCCTCCTCCACGCAGCCCCCTGGACACCCCGCCTGCACCCCTTGCCCGCAGCCTGGGCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53097665..53097936 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116077 RMVar_ID_116077 Human_SNP_ID_815735854 m1A Human chr12 + 53321521 53321521 53321521 CAGTCGGCAAACTCCTGGCCGGAACGGCACAGACCGCACTCCCGCAACTCGGTTCCCGGGCTAGA CAGTCGGCAAACTCCTGGCCGGAACGGCACAGGCCGCACTCCCGCAACTCGGTTCCCGGGCTAGA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53321026..53321575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 116078 RMVar_ID_116078 Human_SNP_ID_815754140 m1A Human chr12 - 49040592 49040592 49040592 ATTGACTCCTCGGCCCCAACCTCCGCCCCCTGAGAGCTGCTGTGCTCTGCCCCCTCGCTCACTGC ATTGACTCCTCGGCCCCAACCTCCGCCCCCTGGGAGCTGCTGTGCTCTGCCCCCTCGCTCACTGC T C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:49040551..49040736 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma,large_intestine ulcerative_colitis 2 large intestine Human_RBP_ID_5127105,Human_RBP_ID_17074814,Human_RBP_ID_18934422,Human_RBP_ID_22794174,Human_RBP_ID_23561711 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_98264,RMVar_hsa_circ_156262,RMVar_hsa_circ_156263,RMVar_hsa_circ_83103,RMVar_hsa_circ_75610,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156264,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_99971,RMVar_hsa_circ_156269,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156268,RMVar_hsa_circ_107500,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482 116079 RMVar_ID_116079 Human_SNP_ID_815760672 m1A Human chr12 - 124342038 124342038 124342038 TGCCTACTACCTGCCCCGACACCTGGCCCCCAACCCCACCTACCCGCACCTGTACCCACCCTACC TGCCTACTACCTGCCCCGACACCTGGCCCCCACCCCCACCTACCCGCACCTGTACCCACCCTACC T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:124341941..124342156 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 5 head and neck Human_RBP_ID_35929,Human_RBP_ID_5171436,Human_RBP_ID_17357803,Human_RBP_ID_18188985,Human_RBP_ID_18934847,Human_RBP_ID_22710131 Human_Splice_Rec_1441356,Human_Splice_Rec_1441448,Human_Splice_Rec_1441516,Human_Splice_Rec_1441586,Human_Splice_Rec_1441678 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_299402 116080 RMVar_ID_116080 Human_SNP_ID_815764406 m1A Human chr12 - 94994238 94994238 94994238 TCTTCCCACCCAGGCCGTCACCGATGGGTTGTATATACTACTGAAATGAATGGCAAAAACACATT TCTTCCCACCCAGGCCGTCACCGATGGGTTGTGTATACTACTGAAATGAATGGCAAAAACACATT T C NDUFA12 Ensembl:ENSG00000184752 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:94994151..94994275 32194978 MeRIP-seq:(Medium) rs570041029 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 3 head and neck Human_RBP_ID_1478882,Human_RBP_ID_1803200,Human_RBP_ID_9323182,Human_RBP_ID_9365311,Human_RBP_ID_12060690,Human_RBP_ID_17241927,Human_RBP_ID_21884722,Human_RBP_ID_23579379,Human_RBP_ID_25015819,Human_RBP_ID_26912632 Human_Splice_Rec_1408236,Human_Splice_Rec_1408237,Human_Splice_Rec_1408243,Human_Splice_Rec_1408250,Human_Splice_Rec_1408251,Human_Splice_Rec_1408256,Human_Splice_Rec_1408257,Human_Splice_Rec_1408266,Human_Splice_Rec_1408267 Human_miRNA_ID_2173680,Human_miRNA_ID_2177124,Human_miRNA_ID_2355620 RMVar_hsa_circ_83213,RMVar_hsa_circ_92643,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822,RMVar_hsa_circ_158820,RMVar_hsa_circ_33685 116081 RMVar_ID_116081 Human_SNP_ID_815766136 m1A Human chr12 - 57211551 57211551 57211551 CTCAGGCATCATTTTGCTGTTCATGGTACAGGAGCCGCCATTGCTGCAGTGGCCGACGCAGGTCA CTCAGGCATCATTTTGCTGTTCATGGTACAGGCGCCGCCATTGCTGCAGTGGCCGACGCAGGTCA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57211476..57211600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116082 RMVar_ID_116082 Human_SNP_ID_815767631 m1A Human chr12 + 14801427 14801427 14801427 GTATGGTTTACTTGTTCATTAAAAAAAGAAAAACCTGTGAAGGTGAAGACAAAGAAATAGCTTAT GTATGGTTTACTTGTTCATTAAAAAAAGAAAAGCCTGTGAAGGTGAAGACAAAGAAATAGCTTAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:14801378..14801464 26863196 MeRIP-seq:(Medium) rs778664253 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116083 RMVar_ID_116083 Human_SNP_ID_815768702 m1A Human chr12 + 48135375 48135375 48135375 TGCAGAGGGGTGGGACGCCATCAGCCTTTGACAGAATTCTGGTAAGTCACTGGGCTGTGTGGCCC TGCAGAGGGGTGGGACGCCATCAGCCTTTGACTGAATTCTGGTAAGTCACTGGGCTGTGTGGCCC A T PFKM Ensembl:ENSG00000152556 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48135276..48135378 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 12 uterus Human_RBP_ID_3941547 Human_Splice_Rec_1361442,Human_Splice_Rec_1361443,Human_Splice_Rec_1361494,Human_Splice_Rec_1361495,Human_Splice_Rec_1361590,Human_Splice_Rec_1361591,Human_Splice_Rec_1361641,Human_Splice_Rec_1361710,Human_Splice_Rec_1361711,Human_Splice_Rec_1361780,Human_Splice_Rec_1361781,Human_Splice_Rec_1361827,Human_Splice_Rec_1361864,Human_Splice_Rec_1361865,Human_Splice_Rec_1361898,Human_Splice_Rec_1361899,Human_Splice_Rec_1362000,Human_Splice_Rec_1362001,Human_Splice_Rec_1362044,Human_Splice_Rec_1362045 RMVar_hsa_circ_60413,RMVar_hsa_circ_31436 116084 RMVar_ID_116084 Human_SNP_ID_815775972 m1A Human chr12 + 49269639 49269639 49269639 TCAACACCTTCTTCAGTGAAACGGGTGCTGGCAAGCATGTGCCCCGGGCAGTGTTTGTAGACTTG TCAACACCTTCTTCAGTGAAACGGGTGCTGGCGAGCATGTGCCCCGGGCAGTGTTTGTAGACTTG A G TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49269589..49269732 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_420851,Human_RBP_ID_754126,Human_RBP_ID_2339944,Human_RBP_ID_8377164,Human_RBP_ID_9017682,Human_RBP_ID_9322496,Human_RBP_ID_18627659,Human_RBP_ID_22435839,Human_RBP_ID_22755889,Human_RBP_ID_23561887 Human_Splice_Rec_1364449,Human_Splice_Rec_1364463,Human_Splice_Rec_1364471,Human_Splice_Rec_1364475,Human_Splice_Rec_1364479,Human_Splice_Rec_1364483 Human_miRNA_ID_1626616,Human_miRNA_ID_1667114 RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_99581,RMVar_hsa_circ_103440,RMVar_hsa_circ_156315,RMVar_hsa_circ_156316,RMVar_hsa_circ_156317 116085 RMVar_ID_116085 Human_SNP_ID_815787544 m1A Human chr12 - 52054780 52054778 52054780 AGAAGTGGCCGAAGGAGCCATCCCAGGGAGAGAGCTGGGGCGGCTGGAAGCTGGGCGTGGAGGGC AGAAGTGGCCGAAGGAGCCATCCCAGGGAGAG__CTGGGGCGGCTGGAAGCTGGGCGTGGAGGGC GCT G MF688637 RNACentral:URS0000DE37B8 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:52054735..52054909 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - 116086 RMVar_ID_116086 Human_SNP_ID_815821952 m1A Human chr12 + 98547765 98547765 98547765 TGGATAAAAATTTTGCTGTTTGTTGTTGTGGCAGTTTTTTTGTTTTTGGTCTATCAAGCTATGGA TGGATAAAAATTTTGCTGTTTGTTGTTGTGGCGGTTTTTTTGTTTTTGGTCTATCAAGCTATGGA A G TMPO Ensembl:ENSG00000120802 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:98545059..98547831 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_295271,Human_RBP_ID_1803868,Human_RBP_ID_2364427,Human_RBP_ID_3418056,Human_RBP_ID_6238612,Human_RBP_ID_9709968,Human_RBP_ID_12068645,Human_RBP_ID_22384103,Human_RBP_ID_22437968,Human_RBP_ID_22910399,Human_RBP_ID_24408081,Human_RBP_ID_24468272,Human_RBP_ID_25028687,Human_RBP_ID_26420820,Human_RBP_ID_27219283,Human_RBP_ID_27635561 RMVar_hsa_circ_159018,RMVar_hsa_circ_99061 116087 RMVar_ID_116087 Human_SNP_ID_815824411 m1A Human chr12 - 124372474 124372474 124372474 GCCGACGGGCCACCCCCAGGGCCACCCACCCCACCACCGGAGGACATCCCGGCCCCCACTGAGCC GCCGACGGGCCACCCCCAGGGCCACCCACCCCGCCACCGGAGGACATCCCGGCCCCCACTGAGCC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:124372426..124372475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 116088 RMVar_ID_116088 Human_SNP_ID_815845135 m1A Human chr12 + 31085125 31085125 31085125 ACGAGAGTGATGAGGAGAAAAAGGTGGCGAGCAGGTGAGACAGAGGCGGTAGCACTACCCTGCCC ACGAGAGTGATGAGGAGAAAAAGGTGGCGAGCGGGTGAGACAGAGGCGGTAGCACTACCCTGCCC A G DDX11 Ensembl:ENSG00000013573 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2536756 Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,THCA,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,liver neoplasm,endometrium endometrioid_carcinoma 25 uterus,liver,pancreas,haematopoietic and lymphoid tissue Human_RBP_ID_809409,Human_RBP_ID_872197,Human_RBP_ID_18976923,Human_RBP_ID_22572313,Human_RBP_ID_26321276 Human_Splice_Rec_1351873,Human_Splice_Rec_1351895,Human_Splice_Rec_1351947,Human_Splice_Rec_1351997,Human_Splice_Rec_1352013,Human_Splice_Rec_1352065,Human_Splice_Rec_1352083,Human_Splice_Rec_1352125,Human_Splice_Rec_1352175,Human_Splice_Rec_1352187,Human_Splice_Rec_1352239,Human_Splice_Rec_1352289,Human_Splice_Rec_1352311 RMVar_hsa_circ_74755,RMVar_hsa_circ_360582,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 116089 RMVar_ID_116089 Human_SNP_ID_815855518 m1A Human chr12 + 56159664 56159664 56159664 AGATCCTGTACAGCCAGTGTGGGGATGTGATGAGGGCCCTGGGCCAGAACCCTACCAACGCCGAG AGATCCTGTACAGCCAGTGTGGGGATGTGATGCGGGCCCTGGGCCAGAACCCTACCAACGCCGAG A C MYL6 Ensembl:ENSG00000092841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:56159576..56159725;chr12:56159576..56159675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 meninges atypical,large_intestine adenocarcinoma 24 large intestine,brain Human_RBP_ID_1474266,Human_RBP_ID_1797566,Human_RBP_ID_4231959,Human_RBP_ID_5111488,Human_RBP_ID_17650418,Human_RBP_ID_17830372,Human_RBP_ID_18629551,Human_RBP_ID_22435961,Human_RBP_ID_22905987,Human_RBP_ID_23207693,Human_RBP_ID_23566569,Human_RBP_ID_26909042 Human_Splice_Rec_1381746,Human_Splice_Rec_1381759,Human_Splice_Rec_1381778,Human_Splice_Rec_1381779,Human_Splice_Rec_1381788,Human_Splice_Rec_1381789,Human_Splice_Rec_1381800,Human_Splice_Rec_1381810,Human_Splice_Rec_1381822,Human_Splice_Rec_1381823,Human_Splice_Rec_1381832,Human_Splice_Rec_1381833,Human_Splice_Rec_1381840,Human_Splice_Rec_1381841,Human_Splice_Rec_1381850,Human_Splice_Rec_1381851,Human_Splice_Rec_1381856,Human_Splice_Rec_1381857,Human_Splice_Rec_1381868,Human_Splice_Rec_1381869,Human_Splice_Rec_1381878,Human_Splice_Rec_1381879,Human_Splice_Rec_1381882,Human_Splice_Rec_1381886,Human_Splice_Rec_1381887,Human_Splice_Rec_1381894,Human_Splice_Rec_1381906,Human_Splice_Rec_1381907 Human_miRNA_ID_1193771,Human_miRNA_ID_2573774,Human_miRNA_ID_2573775 RMVar_hsa_circ_84206,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224,RMVar_hsa_circ_81881,RMVar_hsa_circ_112837,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_157227,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_88064,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_157232,RMVar_hsa_circ_325389,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235 116090 RMVar_ID_116090 Human_SNP_ID_815855521 m1A Human chr12 + 56159664 56159664 56159664 AGATCCTGTACAGCCAGTGTGGGGATGTGATGAGGGCCCTGGGCCAGAACCCTACCAACGCCGAG AGATCCTGTACAGCCAGTGTGGGGATGTGATGGGGGCCCTGGGCCAGAACCCTACCAACGCCGAG A G MYL6 Ensembl:ENSG00000092841 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:56159576..56159725;chr12:56159576..56159675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1474266,Human_RBP_ID_1797566,Human_RBP_ID_4231959,Human_RBP_ID_5111488,Human_RBP_ID_17650418,Human_RBP_ID_17830372,Human_RBP_ID_18629551,Human_RBP_ID_22435961,Human_RBP_ID_22905987,Human_RBP_ID_23207693,Human_RBP_ID_23566569,Human_RBP_ID_26909042 Human_Splice_Rec_1381746,Human_Splice_Rec_1381759,Human_Splice_Rec_1381778,Human_Splice_Rec_1381779,Human_Splice_Rec_1381788,Human_Splice_Rec_1381789,Human_Splice_Rec_1381800,Human_Splice_Rec_1381810,Human_Splice_Rec_1381822,Human_Splice_Rec_1381823,Human_Splice_Rec_1381832,Human_Splice_Rec_1381833,Human_Splice_Rec_1381840,Human_Splice_Rec_1381841,Human_Splice_Rec_1381850,Human_Splice_Rec_1381851,Human_Splice_Rec_1381856,Human_Splice_Rec_1381857,Human_Splice_Rec_1381868,Human_Splice_Rec_1381869,Human_Splice_Rec_1381878,Human_Splice_Rec_1381879,Human_Splice_Rec_1381882,Human_Splice_Rec_1381886,Human_Splice_Rec_1381887,Human_Splice_Rec_1381894,Human_Splice_Rec_1381906,Human_Splice_Rec_1381907 Human_miRNA_ID_1193771,Human_miRNA_ID_2573774,Human_miRNA_ID_2573775 RMVar_hsa_circ_84206,RMVar_hsa_circ_112202,RMVar_hsa_circ_157224,RMVar_hsa_circ_81881,RMVar_hsa_circ_112837,RMVar_hsa_circ_157226,RMVar_hsa_circ_98547,RMVar_hsa_circ_157227,RMVar_hsa_circ_317036,RMVar_hsa_circ_157228,RMVar_hsa_circ_157229,RMVar_hsa_circ_88064,RMVar_hsa_circ_157233,RMVar_hsa_circ_84482,RMVar_hsa_circ_157232,RMVar_hsa_circ_325389,RMVar_hsa_circ_157234,RMVar_hsa_circ_79746,RMVar_hsa_circ_157235 116091 RMVar_ID_116091 Human_SNP_ID_815893565 m1A Human chr12 + 9310388 9310388 9310388 GACAACATCTGCCCCTTGTCATCTGCAGCGGGATCTCCAACCAGCCGCTGGAATTCACCTTCCAG GACAACATCTGCCCCTTGTCATCTGCAGCGGGGTCTCCAACCAGCCGCTGGAATTCACCTTCCAG A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12317441 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_875911,Human_RBP_ID_18527004 Human_Splice_Rec_1337593 RMVar_hsa_circ_44481,RMVar_hsa_circ_107891,RMVar_hsa_circ_154842 116092 RMVar_ID_116092 Human_SNP_ID_815933310 m1A Human chr12 - 49706833 49706833 49706833 CTCGGGACCGACGCCTCCACCGCTGGACCCTTAGGAGAAGTCCCCAGTTCGGGACCGTCCTAGGA CTCGGGACCGACGCCTCCACCGCTGGACCCTTGGGAGAAGTCCCCAGTTCGGGACCGTCCTAGGA T C FMNL3 Ensembl:ENSG00000161791 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49706830..49706935 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_6191497 RMVar_hsa_circ_123896,RMVar_hsa_circ_156359,RMVar_hsa_circ_87831,RMVar_hsa_circ_156367 116093 RMVar_ID_116093 Human_SNP_ID_815934161 m1A Human chr12 + 120469664 120469664 120469664 CCCGCCGCAGCCCACGTCGCCGCCGCCGCCTCAGCACGGGTCCCCCCGCAGCGTCCCCGCGGGCT CCCGCCGCAGCCCACGTCGCCGCCGCCGCCTCTGCACGGGTCCCCCCGCAGCGTCCCCGCGGGCT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:120469384..120469750;chr12:120465569..120469750;chr12:120465576..120469750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 116094 RMVar_ID_116094 Human_SNP_ID_815975256 m1A Human chr12 + 79934972 79934972 79934972 CTGCCGCCGGGTCTTCTTATCGCGAGGGGGGGAAGGGGGAGGCGGAGAGGGAAGAGAGGGGAGGC CTGCCGCCGGGTCTTCTTATCGCGAGGGGGGGGAGGGGGAGGCGGAGAGGGAAGAGAGGGGAGGC A G PPP1R12A-AS1 Ensembl:ENSG00000257557 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:79934933..79935125 26863196 MeRIP-seq:(Medium) rs1225173793 Functional Loss SNV TCGA 33..33 33 UCEC 1 - 116095 RMVar_ID_116095 Human_SNP_ID_815978381 m1A Human chr12 + 69597979 69597979 69597979 TATTGGAATTTTAATCTTTAGGCTGTTCTGAGATGTTGATGGCTCATGCTGTGACACAGCTTGCC TATTGGAATTTTAATCTTTAGGCTGTTCTGAGCTGTTGATGGCTCATGCTGTGACACAGCTTGCC A C CCT2 Ensembl:ENSG00000166226 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_1477097,Human_RBP_ID_1800719,Human_RBP_ID_12023785,Human_RBP_ID_17826039,Human_RBP_ID_18263777,Human_RBP_ID_18434734,Human_RBP_ID_22437333,Human_RBP_ID_22646731,Human_RBP_ID_23572897,Human_RBP_ID_25000444,Human_RBP_ID_27632920 Human_Splice_Rec_1396842,Human_Splice_Rec_1396843,Human_Splice_Rec_1396878,Human_Splice_Rec_1396879,Human_Splice_Rec_1396934,Human_Splice_Rec_1396935 RMVar_hsa_circ_113475,RMVar_hsa_circ_158186,RMVar_hsa_circ_114979,RMVar_hsa_circ_158191,RMVar_hsa_circ_349898,RMVar_hsa_circ_158196,RMVar_hsa_circ_98434,RMVar_hsa_circ_158199,RMVar_hsa_circ_377847,RMVar_hsa_circ_158200 116096 RMVar_ID_116096 Human_SNP_ID_815997979 m1A Human chr12 + 14789129 14789129 14789129 CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGAGCTCCTGAAAAGAGAAAAATGATAAATTAATG CCTGGCATTCCAGGTGGTCTCAGGAATGGAGGTGCTCCTGAAAAGAGAAAAATGATAAATTAATG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:14789032..14789166 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116097 RMVar_ID_116097 Human_SNP_ID_816005627 m1A Human chr12 + 131395654 131395654 131395654 TGGTGATGATGATGGTGATGATGGTGATGATGATGGTGATGGTGATGGTGATGATGGTGATGGTG TGGTGATGATGATGGTGATGATGGTGATGATGGTGGTGATGGTGATGGTGATGATGGTGATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:131395606..131395831 26863196 MeRIP-seq:(Medium) rs142796441 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 116098 RMVar_ID_116098 Human_SNP_ID_816006893 m1A Human chr12 - 123364807 123364807 123364807 CAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGACGCCGCTGCTGCCGCCGCCACCGCCGCCTCCG CAAGATGGCGGCGGGGAGGTAGGCAGAGCAGGTCGCCGCTGCTGCCGCCGCCACCGCCGCCTCCG T A MIR8072,SBNO1 Ensembl:ENSG00000284425,Ensembl:ENSG00000139697 miRNA,Protein coding exon,5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:123364722..123364887 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_230030,Human_RBP_ID_4247115,Human_RBP_ID_8787016,Human_RBP_ID_9279345,Human_RBP_ID_17357423,Human_RBP_ID_18457105 116099 RMVar_ID_116099 Human_SNP_ID_816007159 m1A Human chr12 - 14771105 14771105 14771105 GCAATCACAGTGGGCAGCCCGATTTTCTGCTGAGTAGGCGCTGTGATTTCAGAATGTCTGGGCGA GCAATCACAGTGGGCAGCCCGATTTTCTGCTGGGTAGGCGCTGTGATTTCAGAATGTCTGGGCGA T C H4-16 Ensembl:ENSG00000197837 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:14771101..14771125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_1468949,Human_RBP_ID_3399824,Human_RBP_ID_4215307,Human_RBP_ID_8370942,Human_RBP_ID_22040281,Human_RBP_ID_22172693,Human_RBP_ID_23550307,Human_RBP_ID_26904825 116100 RMVar_ID_116100 Human_SNP_ID_816022111 m1A Human chr12 + 56007546 56007546 56007546 GTGAAGCTGCTGATGGAGATGGAGCCGCCGCCACCGCCGCCTCTGAGCGCCCGGGTCCTGGCTCC GTGAAGCTGCTGATGGAGATGGAGCCGCCGCCGCCGCCGCCTCTGAGCGCCCGGGTCCTGGCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:56007496..56007657 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_4231566 116101 RMVar_ID_116101 Human_SNP_ID_816032037 m1A Human chr12 - 2890974 2890974 2890974 GCCACGGCCCTGTCTGACCTGTCGCCGCTGGGACTGAGCCGGCAGCGCGAAGCCTCCATGCCCGC GCCACGGCCCTGTCTGACCTGTCGCCGCTGGGCCTGAGCCGGCAGCGCGAAGCCTCCATGCCCGC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:2890951..2890975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 116102 RMVar_ID_116102 Human_SNP_ID_816035419 m1A Human chr12 + 54183939 54183939 54183939 CATGGATGGACCCCAGCAGGAAAGCCTGGGGCATATGTCCATGCCGCTGTCACCTGGGAAAAGAG CATGGATGGACCCCAGCAGGAAAGCCTGGGGCGTATGTCCATGCCGCTGTCACCTGGGAAAAGAG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54183777..54183957 26863196 MeRIP-seq:(Medium) rs747175374 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 11 large intestine 116103 RMVar_ID_116103 Human_SNP_ID_816048614 m1A Human chr12 + 53382473 53382472 53382474 CTGGAGTGATGCCTAATATTCAGTATCAAGTAATCCCACAGTTCCAGACCGTTGATGGGCAACAG CTGGAGTGATGCCTAATATTCAGTATCAAGTA__CCCACAGTTCCAGACCGTTGATGGGCAACAG AAT A SP1 Ensembl:ENSG00000185591 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53382426..53382676 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 HNSC 1 - Human_RBP_ID_422265,Human_RBP_ID_1473432,Human_RBP_ID_5139856,Human_RBP_ID_8782845,Human_RBP_ID_17239057,Human_RBP_ID_17821679,Human_RBP_ID_18628732,Human_RBP_ID_27630408 RMVar_hsa_circ_81010,RMVar_hsa_circ_156934,RMVar_hsa_circ_85364,RMVar_hsa_circ_108173,RMVar_hsa_circ_156935,RMVar_hsa_circ_156936,RMVar_hsa_circ_78974,RMVar_hsa_circ_156938,RMVar_hsa_circ_305340,RMVar_hsa_circ_315418,RMVar_hsa_circ_156937,RMVar_hsa_circ_156939 116104 RMVar_ID_116104 Human_SNP_ID_816062145 m1A Human chr12 + 6492971 6492971 6492971 AGAGTGAGCCTTATACCGATCAATCTAGGCACACCTGGGGATGGGGAAGGGAGGGAATTAATCTG AGAGTGAGCCTTATACCGATCAATCTAGGCACCCCTGGGGATGGGGAAGGGAGGGAATTAATCTG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6492851..6492975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 8 kidney 116105 RMVar_ID_116105 Human_SNP_ID_816094100 m1A Human chr12 + 57522759 57522759 57522759 CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGACGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA CGGCGGCTCCTGCGGCGGCGGCTGCGGCAGCGGCGGCGGCGGCGGCAGCGGCAGCAGCCTGCGCA A G MBD6 Ensembl:ENSG00000166987 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr12:57522740..57522822 26863410 MeRIP-seq:(Medium) rs181698936 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_4234743 116106 RMVar_ID_116106 Human_SNP_ID_816120929 m1A Human chr12 - 56688058 56688058 56688058 AGTCGCCACCGGAGAGAAGTCGACTCCCTAGCAGCAGCCGCCGCCAGAGAGGCCCGCCCACCAGT AGTCGCCACCGGAGAGAAGTCGACTCCCTAGCTGCAGCCGCCGCCAGAGAGGCCCGCCCACCAGT T A PTGES3 Ensembl:ENSG00000110958 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:56687942..56688335;chr12:56687939..56688325 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_33845,Human_RBP_ID_228650,Human_RBP_ID_424339,Human_RBP_ID_878662,Human_RBP_ID_1474752,Human_RBP_ID_1798013,Human_RBP_ID_4233744,Human_RBP_ID_5461990,Human_RBP_ID_6202008,Human_RBP_ID_11991347,Human_RBP_ID_18630128,Human_RBP_ID_22437852,Human_RBP_ID_22493664,Human_RBP_ID_22532501,Human_RBP_ID_26321632,Human_RBP_ID_26909561,Human_RBP_ID_27216763 Human_Splice_Rec_1385211,Human_Splice_Rec_1385227,Human_Splice_Rec_1385241,Human_Splice_Rec_1385253,Human_Splice_Rec_1385265,Human_Splice_Rec_1385277 RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 116107 RMVar_ID_116107 Human_SNP_ID_816127605 m1A Human chr12 + 45413249 45413249 45413249 TTTAGGAGGCTACAGCAGGTAACCCAGACAACAAGTGATAGGTGCCTAAATAGTGGGCATAGGAG TTTAGGAGGCTACAGCAGGTAACCCAGACAACGAGTGATAGGTGCCTAAATAGTGGGCATAGGAG A G ANO6 Ensembl:ENSG00000177119 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:45413201..45413353 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_34990,RMVar_hsa_circ_68423,RMVar_hsa_circ_90302,RMVar_hsa_circ_156029,RMVar_hsa_circ_85655,RMVar_hsa_circ_97007,RMVar_hsa_circ_156030,RMVar_hsa_circ_340494,RMVar_hsa_circ_156032,RMVar_hsa_circ_156033,RMVar_hsa_circ_328966 116108 RMVar_ID_116108 Human_SNP_ID_816149940 m1A Human chr12 - 6602392 6602392 6602392 GAAACCTCGGGACCCTAAAATCCCTAAGAGCAAGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA GAAACCTCGGGACCCTAAAATCCCTAAGAGCACGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA T G CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6602376..6602539 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 22 large intestine Human_RBP_ID_9364600,Human_RBP_ID_18434662,Human_RBP_ID_24543045,Human_RBP_ID_26321162,Human_RBP_ID_26910589 Human_Splice_Rec_1329263,Human_Splice_Rec_1329391,Human_Splice_Rec_1329466,Human_Splice_Rec_1329467,Human_Splice_Rec_1329543,Human_Splice_Rec_1329621,Human_Splice_Rec_1329711,Human_Splice_Rec_1329897,Human_Splice_Rec_1330003,Human_Splice_Rec_1330123,Human_Splice_Rec_1330199,Human_Splice_Rec_1330277,Human_Splice_Rec_1330377,Human_Splice_Rec_1330451,Human_Splice_Rec_1330527,Human_Splice_Rec_1330853,Human_Splice_Rec_1330977,Human_Splice_Rec_1331041,Human_Splice_Rec_1331231,Human_Splice_Rec_1331243,Human_Splice_Rec_1331249 RMVar_hsa_circ_24388,RMVar_hsa_circ_46896,RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 116109 RMVar_ID_116109 Human_SNP_ID_816149942 m1A Human chr12 - 6602392 6602392 6602392 GAAACCTCGGGACCCTAAAATCCCTAAGAGCAAGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA GAAACCTCGGGACCCTAAAATCCCTAAGAGCATGCGCCAAAAAAAGGAGGTGAGTGGGTGACTGA T A CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6602376..6602539 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 12 large intestine Human_RBP_ID_9364600,Human_RBP_ID_18434662,Human_RBP_ID_24543045,Human_RBP_ID_26321162,Human_RBP_ID_26910589 Human_Splice_Rec_1329263,Human_Splice_Rec_1329391,Human_Splice_Rec_1329466,Human_Splice_Rec_1329467,Human_Splice_Rec_1329543,Human_Splice_Rec_1329621,Human_Splice_Rec_1329711,Human_Splice_Rec_1329897,Human_Splice_Rec_1330003,Human_Splice_Rec_1330123,Human_Splice_Rec_1330199,Human_Splice_Rec_1330277,Human_Splice_Rec_1330377,Human_Splice_Rec_1330451,Human_Splice_Rec_1330527,Human_Splice_Rec_1330853,Human_Splice_Rec_1330977,Human_Splice_Rec_1331041,Human_Splice_Rec_1331231,Human_Splice_Rec_1331243,Human_Splice_Rec_1331249 RMVar_hsa_circ_24388,RMVar_hsa_circ_46896,RMVar_hsa_circ_107940,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 116110 RMVar_ID_116110 Human_SNP_ID_816150385 m1A Human chr12 + 52054450 52054450 52054450 CATCAAGCCCACCATGGACCTGGCCAGCCCCGAGGCAGCCCCCGCTGCCCCCACTGCCCTGCCCA CATCAAGCCCACCATGGACCTGGCCAGCCCCGGGGCAGCCCCCGCTGCCCCCACTGCCCTGCCCA A G NR4A1 Ensembl:ENSG00000123358 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:52054401..52054575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma,lung acinar_adenocarcinoma 28 lung,breast Human_RBP_ID_228863,Human_RBP_ID_27422785 RMVar_hsa_circ_79002,RMVar_hsa_circ_76916,RMVar_hsa_circ_156653,RMVar_hsa_circ_82671,RMVar_hsa_circ_156654,RMVar_hsa_circ_156655 116111 RMVar_ID_116111 Human_SNP_ID_816159812 m1A Human chr12 - 124340141 124340141 124340141 GGGTGGGGGCAGCAGCAGCCGCCCCGCCTCCCACTCCCATGCCCACCAGCACTCGCCCATCTCCC GGGTGGGGGCAGCAGCAGCCGCCCCGCCTCCCCCTCCCATGCCCACCAGCACTCGCCCATCTCCC T G NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:124340126..124340150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 5 lung Human_RBP_ID_35927,Human_RBP_ID_3420805,Human_RBP_ID_3943827,Human_RBP_ID_22532531,Human_RBP_ID_23208306 Human_Splice_Rec_1441362,Human_Splice_Rec_1441454,Human_Splice_Rec_1441522,Human_Splice_Rec_1441592,Human_Splice_Rec_1441684,Human_Splice_Rec_1441746,Human_Splice_Rec_1441754 Human_miRNA_ID_2051960,Human_miRNA_ID_2493398,Human_miRNA_ID_2775025,Human_miRNA_ID_2873586,Human_miRNA_ID_2981549 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_339890,RMVar_hsa_circ_368275,RMVar_hsa_circ_299402 116112 RMVar_ID_116112 Human_SNP_ID_816165500 m1A Human chr12 - 49653275 49653261 49653275 CCTAGAGAATGAAAACATGATGCGGGTGGCAGAACTAGAGAAGCAGCTGCTACAGCGGGAGAAGG CCTAGAGAATGAAAACATGATGCGGGTGGCAG______________CTGCTACAGCGGGAGAAGG GCTGCTTCTCTAGTT G FMNL3 Ensembl:ENSG00000161791 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:49653198..49653333 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..46 33 BRCA 1 - Human_RBP_ID_27806620 Human_Splice_Rec_1365630,Human_Splice_Rec_1365631,Human_Splice_Rec_1365680,Human_Splice_Rec_1365681,Human_Splice_Rec_1365750,Human_Splice_Rec_1365751 Human_miRNA_ID_3117898 RMVar_hsa_circ_35809,RMVar_hsa_circ_31844,RMVar_hsa_circ_28763,RMVar_hsa_circ_126265,RMVar_hsa_circ_82280,RMVar_hsa_circ_156357,RMVar_hsa_circ_156358,RMVar_hsa_circ_16103 116113 RMVar_ID_116113 Human_SNP_ID_816170416 m1A Human chr12 + 118138088 118138088 118138088 CAGCATTTCGTGGGATGGTCTTGATTCAGGGAAGCTCTACACCTTGGTCCTGACAGACCCGGATG CAGCATTTCGTGGGATGGTCTTGATTCAGGGAGGCTCTACACCTTGGTCCTGACAGACCCGGATG A G PEBP1 Ensembl:ENSG00000089220 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:118137975..118138175 26863196 MeRIP-seq:(Medium) rs779234877 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_411840,Human_RBP_ID_1356218,Human_RBP_ID_1465590,Human_RBP_ID_9012013,Human_RBP_ID_11836498,Human_RBP_ID_17830579,Human_RBP_ID_22437449,Human_RBP_ID_22756150,Human_RBP_ID_26901735 Human_Splice_Rec_1431132,Human_Splice_Rec_1431133 Human_miRNA_ID_2697479,Human_miRNA_ID_3001599 RMVar_hsa_circ_110913,RMVar_hsa_circ_121207,RMVar_hsa_circ_374555,RMVar_hsa_circ_160564,RMVar_hsa_circ_301584,RMVar_hsa_circ_160565,RMVar_hsa_circ_160566,RMVar_hsa_circ_160567 116114 RMVar_ID_116114 Human_SNP_ID_816172533 m1A Human chr12 + 6915771 6915770 6915771 GCCTCCCGCCCCGCCCATTGATCTCAGGCTCCACCCCTCTAAGCCTCTTATCTTTCTCCTTCCTT GCCTCCCGCCCCGCCCATTGATCTCAGGCTCC_CCCCTCTAAGCCTCTTATCTTTCTCCTTCCTT CA C ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6915769..6915898 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_5127069,Human_RBP_ID_17075035,Human_RBP_ID_22538511,Human_RBP_ID_22644601 116115 RMVar_ID_116115 Human_SNP_ID_816181191 m1A Human chr12 + 28452582 28452582 28452582 CATGCTGAAGAAAGGGAATTATGGAAGACAGAACATGCAAAAGATCAAGAAAAAGTATCTCAGGA CATGCTGAAGAAAGGGAATTATGGAAGACAGAGCATGCAAAAGATCAAGAAAAAGTATCTCAGGA A G CCDC91 Ensembl:ENSG00000123106 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:28452536..28452685 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_1479522,Human_RBP_ID_23555118,Human_RBP_ID_26321264,Human_RBP_ID_27805330 Human_Splice_Rec_1350367,Human_Splice_Rec_1350393,Human_Splice_Rec_1350415,Human_Splice_Rec_1350471,Human_Splice_Rec_1350517,Human_Splice_Rec_1350557,Human_Splice_Rec_1350579,Human_Splice_Rec_1350599,Human_Splice_Rec_1350601 Human_miRNA_ID_1309193,Human_miRNA_ID_1688924 RMVar_hsa_circ_355108,RMVar_hsa_circ_68151,RMVar_hsa_circ_331879,RMVar_hsa_circ_366179,RMVar_hsa_circ_55096,RMVar_hsa_circ_293054,RMVar_hsa_circ_278642,RMVar_hsa_circ_95347,RMVar_hsa_circ_155538,RMVar_hsa_circ_110591,RMVar_hsa_circ_5211,RMVar_hsa_circ_155543,RMVar_hsa_circ_287767,RMVar_hsa_circ_273786,RMVar_hsa_circ_155545,RMVar_hsa_circ_155546,RMVar_hsa_circ_282674,RMVar_hsa_circ_61899,RMVar_hsa_circ_307642,RMVar_hsa_circ_155547 116116 RMVar_ID_116116 Human_SNP_ID_816187014 m1A Human chr12 - 53297910 53297910 53297910 CCACATGCTCTCACTCACCTTCTCTACATAGTACCCAGTTCCCACATCGATGAGCACGTGTTCCA CCACATGCTCTCACTCACCTTCTCTACATAGTGCCCAGTTCCCACATCGATGAGCACGTGTTCCA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53297816..53298199 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 116117 RMVar_ID_116117 Human_SNP_ID_816194574 m1A Human chr12 - 55794882 55794882 55794882 CTTTTTTTTCTCCCTTTTGTCTATTTTTACTTAGAGAATGCAGAAGAGGGCTGAACGATTCAATG CTTTTTTTTCTCCCTTTTGTCTATTTTTACTTTGAGAATGCAGAAGAGGGCTGAACGATTCAATG T A AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:55794870..55794941;chr12:55794851..55794900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_36154,Human_RBP_ID_194784,Human_RBP_ID_873076,Human_RBP_ID_2344822,Human_RBP_ID_11983020,Human_RBP_ID_22572701,Human_RBP_ID_25016189 Human_Splice_Rec_1379271,Human_Splice_Rec_1379291,Human_Splice_Rec_1379313,Human_Splice_Rec_1379335,Human_Splice_Rec_1379353,Human_Splice_Rec_1379375 RMVar_hsa_circ_36264,RMVar_hsa_circ_122717,RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_296409,RMVar_hsa_circ_343802,RMVar_hsa_circ_315736,RMVar_hsa_circ_276457,RMVar_hsa_circ_157118,RMVar_hsa_circ_157119,RMVar_hsa_circ_157117,RMVar_hsa_circ_310136,RMVar_hsa_circ_157121 116118 RMVar_ID_116118 Human_SNP_ID_816201284 m1A Human chr12 + 131753272 131753272 131753272 TGACCGTGTCTAACTCCCCTGGAGTGACGACCACCGCCCCACCACCTCCTGGGACCACACCACTA TGACCGTGTCTAACTCCCCTGGAGTGACGACCCCCGCCCCACCACCTCCTGGGACCACACCACTA A C SFSWAP Ensembl:ENSG00000061936 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:131753224..131753414;chr12:131753223..131753395 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_8369728,Human_RBP_ID_9013457,Human_RBP_ID_9365848 Human_Splice_Rec_1445233,Human_Splice_Rec_1445267,Human_Splice_Rec_1445293,Human_Splice_Rec_1445319,Human_Splice_Rec_1445349 RMVar_hsa_circ_51181,RMVar_hsa_circ_6093,RMVar_hsa_circ_50163,RMVar_hsa_circ_52589,RMVar_hsa_circ_49579,RMVar_hsa_circ_161737,RMVar_hsa_circ_161739,RMVar_hsa_circ_293726,RMVar_hsa_circ_375465,RMVar_hsa_circ_284835,RMVar_hsa_circ_161738 116119 RMVar_ID_116119 Human_SNP_ID_816204527 m1A Human chr12 - 132689211 132689211 132689211 CCCGCTCCCCTGGCCCTGTCTTCACCCGCACCACGCAGACCCGCTCCCTTGGCCCTGTCTTTACC CCCGCTCCCCTGGCCCTGTCTTCACCCGCACCCCGCAGACCCGCTCCCTTGGCCCTGTCTTTACC T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:132689197..132689512 26863196 MeRIP-seq:(Medium) rs1379203903 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 116120 RMVar_ID_116120 Human_SNP_ID_816209989 m1A Human chr12 - 123937028 123937028 123937028 TGAAGCCCGCCGTGCCCCACCCCGCGCTGTCCATGCACTGTGAGCACCACTGGGAAATCTCAGCC TGAAGCCCGCCGTGCCCCACCCCGCGCTGTCCTTGCACTGTGAGCACCACTGGGAAATCTCAGCC T A CCDC92 Ensembl:ENSG00000119242 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123936986..123937093 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_414238,Human_RBP_ID_27211913 Human_miRNA_ID_330776,Human_miRNA_ID_347885,Human_miRNA_ID_1072082,Human_miRNA_ID_1996086,Human_miRNA_ID_2078922,Human_miRNA_ID_2081238,Human_miRNA_ID_2091784,Human_miRNA_ID_2228579,Human_miRNA_ID_2286010,Human_miRNA_ID_2289008,Human_miRNA_ID_2504557 RMVar_hsa_circ_86596,RMVar_hsa_circ_97032,RMVar_hsa_circ_161492,RMVar_hsa_circ_79108,RMVar_hsa_circ_161493,RMVar_hsa_circ_161491 116121 RMVar_ID_116121 Human_SNP_ID_816213720 m1A Human chr12 - 124913774 124913774 124913774 TAAATTCTGGCCGTTTTTGGCTTTTTTGTTAGACAATGCAGATCTTCGTGAAGACTCTGACTGGT TAAATTCTGGCCGTTTTTGGCTTTTTTGTTAGTCAATGCAGATCTTCGTGAAGACTCTGACTGGT T A UBC Ensembl:ENSG00000150991 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124913751..124913775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,endometrium endometrioid_carcinoma 30 uterus,haematopoietic and lymphoid tissue Human_RBP_ID_35140,Human_RBP_ID_4247142,Human_RBP_ID_5171558,Human_RBP_ID_18189010,Human_RBP_ID_19057151,Human_RBP_ID_22039722,Human_RBP_ID_23113356,Human_RBP_ID_23207932 Human_Splice_Rec_1442072,Human_Splice_Rec_1442076,Human_Splice_Rec_1442080,Human_Splice_Rec_1442082,Human_Splice_Rec_1442086,Human_Splice_Rec_1442088,Human_Splice_Rec_1442090,Human_Splice_Rec_1442094,Human_Splice_Rec_1442096,Human_Splice_Rec_1442098,Human_Splice_Rec_1442104 Human_miRNA_ID_2445627,Human_miRNA_ID_2447013 RMVar_hsa_circ_94375,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161585,RMVar_hsa_circ_109560,RMVar_hsa_circ_161586 116122 RMVar_ID_116122 Human_SNP_ID_816246076 m1A Human chr12 - 69239676 69239676 69239676 ACCTGGTTGAACTCTTCGCCGACATCCGCGTAAATGTCTATGTGGTCCACGCCGTCCGCCATCTT ACCTGGTTGAACTCTTCGCCGACATCCGCGTACATGTCTATGTGGTCCACGCCGTCCGCCATCTT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:69239576..69239772 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,gastroesophageal_junction adenocarcinoma 4 stomach 116123 RMVar_ID_116123 Human_SNP_ID_816246577 m1A Human chr12 - 31103683 31103683 31103683 ATGGCGGGGCCAAAGGTAGCTTTGACCTCCACACGGGCTCGGATCCAGGCCGGCAGCTTGGCCAG ATGGCGGGGCCAAAGGTAGCTTTGACCTCCACGCGGGCTCGGATCCAGGCCGGCAGCTTGGCCAG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr12:31103633..31103732;chr12:31103594..31103695 26863196,32194978 MeRIP-seq:(Medium) rs781237110 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma,gastroesophageal_junction adenocarcinoma 4 stomach 116124 RMVar_ID_116124 Human_SNP_ID_816246645 m1A Human chr12 + 6536717 6536717 6536717 TTTACATGTTCCAATATGATTCCACCCATGGCAAATTCCATGGCACCGTCAAGGCTGAGAACGGG TTTACATGTTCCAATATGATTCCACCCATGGCGAATTCCATGGCACCGTCAAGGCTGAGAACGGG A G GAPDH Ensembl:ENSG00000111640 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6536476..6536800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_425978,Human_RBP_ID_1358324,Human_RBP_ID_1475987,Human_RBP_ID_1799234,Human_RBP_ID_2349578,Human_RBP_ID_3411529,Human_RBP_ID_8247798,Human_RBP_ID_8381909,Human_RBP_ID_9019893,Human_RBP_ID_12009524,Human_RBP_ID_17240165,Human_RBP_ID_17355702,Human_RBP_ID_17473117,Human_RBP_ID_17824878,Human_RBP_ID_18188677,Human_RBP_ID_22435745,Human_RBP_ID_23570497,Human_RBP_ID_26805387,Human_RBP_ID_27154958,Human_RBP_ID_27424443 Human_Splice_Rec_1328606,Human_Splice_Rec_1328607,Human_Splice_Rec_1328622,Human_Splice_Rec_1328638,Human_Splice_Rec_1328639,Human_Splice_Rec_1328652,Human_Splice_Rec_1328653,Human_Splice_Rec_1328668,Human_Splice_Rec_1328680,Human_Splice_Rec_1328692,Human_Splice_Rec_1328693,Human_Splice_Rec_1328706,Human_Splice_Rec_1328712,Human_Splice_Rec_1328713,Human_Splice_Rec_1328724,Human_Splice_Rec_1328725 RMVar_hsa_circ_88042,RMVar_hsa_circ_154536,RMVar_hsa_circ_90016,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_154540,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537,RMVar_hsa_circ_100729,RMVar_hsa_circ_105081,RMVar_hsa_circ_96984,RMVar_hsa_circ_120054,RMVar_hsa_circ_125986,RMVar_hsa_circ_154542,RMVar_hsa_circ_154543,RMVar_hsa_circ_154544,RMVar_hsa_circ_154541,RMVar_hsa_circ_120781,RMVar_hsa_circ_96003,RMVar_hsa_circ_154547,RMVar_hsa_circ_154548,RMVar_hsa_circ_154549,RMVar_hsa_circ_154546,RMVar_hsa_circ_85578,RMVar_hsa_circ_109934,RMVar_hsa_circ_374391,RMVar_hsa_circ_374726,RMVar_hsa_circ_124027,RMVar_hsa_circ_88412,RMVar_hsa_circ_154552,RMVar_hsa_circ_154554,RMVar_hsa_circ_49293,RMVar_hsa_circ_154555,RMVar_hsa_circ_154553,RMVar_hsa_circ_154550,RMVar_hsa_circ_154551 116125 RMVar_ID_116125 Human_SNP_ID_816251381 m1A Human chr12 + 53669198 53669198 53669198 AGGCTCCCAAACACAGTTCCAATCCCAGCCCCAGAACCAGCCACCCCAACTGTGGCAGCCCCAGC AGGCTCCCAAACACAGTTCCAATCCCAGCCCCCGAACCAGCCACCCCAACTGTGGCAGCCCCAGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:53669126..53669350 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 8 lung 116126 RMVar_ID_116126 Human_SNP_ID_816251898 m1A Human chr12 + 45729703 45729703 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGGCCCATGACTGAGCCCCGCCGCCGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs868266376 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_18417435 116127 RMVar_ID_116127 Human_SNP_ID_816251900 m1A Human chr12 + 45729703 45729703 45729703 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCACCGCCGGCCCATGACTGAGCCCCGCCGCCGCC CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCCCCGCCGGCCCATGACTGAGCCCCGCCGCCGCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:45729643..45729795 26863196 MeRIP-seq:(Medium) rs868266376 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_18417435 116128 RMVar_ID_116128 Human_SNP_ID_816260254 m1A Human chr12 - 30709719 30709719 30709719 GTGAAAAATCAAGCTGAATGACAATTAGCACTAATCTGGCACTTTATAAATTGTGATGTAGCCTC GTGAAAAATCAAGCTGAATGACAATTAGCACTTATCTGGCACTTTATAAATTGTGATGTAGCCTC T A CAPRIN2 Ensembl:ENSG00000110888 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7032 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5111681,Human_RBP_ID_6174339,Human_RBP_ID_18160168 Human_miRNA_ID_778970,Human_miRNA_ID_1751051,Human_miRNA_ID_1942745,Human_miRNA_ID_1945791,Human_miRNA_ID_2063351,Human_miRNA_ID_2116936,Human_miRNA_ID_2200514,Human_miRNA_ID_2203578,Human_miRNA_ID_2448720,Human_miRNA_ID_2816039,Human_miRNA_ID_2863302,Human_miRNA_ID_2901015,Human_miRNA_ID_3113031 RMVar_hsa_circ_155622,RMVar_hsa_circ_99386 116129 RMVar_ID_116129 Human_SNP_ID_816272139 m1A Human chr12 - 12111065 12111049 12111065 GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGGAGGCGCGCGGCGGAGGCGGCTGCGGCGAGCAAG GATAAAGCTGCCGGAGTCCGCGGCGGCGGAGG________________CGGCTGCGGCGAGCAAG GCCTCCGCCGCGCGCCT G - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr12:12111024..12111128 26863410 MeRIP-seq:(Medium) rs570715828 Functional Loss DEL ICGC 33..48 33 PEME 1 - 116130 RMVar_ID_116130 Human_SNP_ID_816279178 m1A Human chr12 - 56160641 56160641 56160641 TACCCGCCCCATGGGCCCGTCACCCCGACAGGATATGCCTCACAAACGCTGCAGGAAGGAAGAGA TACCCGCCCCATGGGCCCGTCACCCCGACAGGCTATGCCTCACAAACGCTGCAGGAAGGAAGAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56160637..56160837 32194978 MeRIP-seq:(Medium) rs767980073 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 13 prostate 116131 RMVar_ID_116131 Human_SNP_ID_816279489 m1A Human chr12 - 56170154 56170152 56170155 TCGGGTGGAAGGCCAGGCCACAGATGAGAAGAAGGAGCCCAAGGTATAGAGGGATTTCTGGAAGC TCGGGTGGAAGGCCAGGCCACAGATGAGAAG___GAGCCCAAGGTATAGAGGGATTTCTGGAAGC CCTT C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr12:56170126..56170225;chr12:56169601..56170283 26863196 MeRIP-seq:(Medium) rs368938279 Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_228273,Human_RBP_ID_260080,Human_RBP_ID_3941762,Human_RBP_ID_5521551,Human_RBP_ID_5558011,Human_RBP_ID_6240777,Human_RBP_ID_9279671,Human_RBP_ID_18977312,Human_RBP_ID_22910751,Human_RBP_ID_24543071,Human_RBP_ID_26321538 Human_Splice_Rec_1381966,Human_Splice_Rec_1381967,Human_Splice_Rec_1382022,Human_Splice_Rec_1382023,Human_Splice_Rec_1382080,Human_Splice_Rec_1382081,Human_Splice_Rec_1382136,Human_Splice_Rec_1382137,Human_Splice_Rec_1382190,Human_Splice_Rec_1382191 RMVar_hsa_circ_35361,RMVar_hsa_circ_116143,RMVar_hsa_circ_301177,RMVar_hsa_circ_346506,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882,RMVar_hsa_circ_341930,RMVar_hsa_circ_157242,RMVar_hsa_circ_157243 116132 RMVar_ID_116132 Human_SNP_ID_816311841 m1A Human chr12 + 46268965 46268964 46268965 CCGCAACCATGGCTTGTGATGGTTTAACGCGGACAGGCCATTCCTCCCCGTCCCGCGCGCGGTCT CCGCAACCATGGCTTGTGATGGTTTAACGCGG_CAGGCCATTCCTCCCCGTCCCGCGCGCGGTCT GA G lnc-ARID2-8 RNACentral:URS00008BCCFF lincRNA exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:46268601..46269111 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BRCA 1 - 116133 RMVar_ID_116133 Human_SNP_ID_816324999 m1A Human chr12 + 121352225 121352225 121352225 CCTCGCCTGTGCGGCTCATCTCGTTCAGCAGCACCAGCACCGCGATCTTGTACGGCGTCACCCAG CCTCGCCTGTGCGGCTCATCTCGTTCAGCAGCGCCAGCACCGCGATCTTGTACGGCGTCACCCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:121352176..121352450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 116134 RMVar_ID_116134 Human_SNP_ID_816325435 m1A Human chr12 - 55828541 55828539 55828541 TGGACCCTGAAATACCTTCATTCTCAGGACTCAGGGACTCAGCAGGGACTGCTCCTAATGGTACC TGGACCCTGAAATACCTTCATTCTCAGGACTC__GGACTCAGCAGGGACTGCTCCTAATGGTACC CCT C DNAJC14 Ensembl:ENSG00000135392 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:55828424..55829151 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 BRCA 1 - Human_RBP_ID_36719,Human_RBP_ID_423335,Human_RBP_ID_1474139,Human_RBP_ID_1797469,Human_RBP_ID_4246722,Human_RBP_ID_6199596,Human_RBP_ID_8783336,Human_RBP_ID_9018608,Human_RBP_ID_11983635,Human_RBP_ID_17239526,Human_RBP_ID_17355203,Human_RBP_ID_17472394,Human_RBP_ID_18629375,Human_RBP_ID_27216220,Human_RBP_ID_27423367 116135 RMVar_ID_116135 Human_SNP_ID_816345829 m1A Human chr12 - 120140915 120140915 120140915 AGGAAGGCCTGAGGTCTCAGAAGAGCGATGAGAGGCAGGGTGTGTGCATTGGCCTAAGTGAGATC AGGAAGGCCTGAGGTCTCAGAAGAGCGATGAGGGGCAGGGTGTGTGCATTGGCCTAAGTGAGATC T C GCN1 Ensembl:ENSG00000089154 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:120140830..120140968 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cervix small_cell_carcinoma 1 uterus Human_RBP_ID_33581,Human_RBP_ID_9279280,Human_RBP_ID_26901870 Human_Splice_Rec_1432357 Human_miRNA_ID_2428969,Human_miRNA_ID_2488770 RMVar_hsa_circ_49715,RMVar_hsa_circ_160653,RMVar_hsa_circ_111513,RMVar_hsa_circ_101268,RMVar_hsa_circ_160654,RMVar_hsa_circ_93383,RMVar_hsa_circ_87631,RMVar_hsa_circ_120788,RMVar_hsa_circ_160656,RMVar_hsa_circ_98965,RMVar_hsa_circ_113123,RMVar_hsa_circ_160657,RMVar_hsa_circ_160658,RMVar_hsa_circ_100597,RMVar_hsa_circ_84498,RMVar_hsa_circ_160672,RMVar_hsa_circ_49551,RMVar_hsa_circ_121438,RMVar_hsa_circ_160659,RMVar_hsa_circ_160661,RMVar_hsa_circ_160662,RMVar_hsa_circ_160660,RMVar_hsa_circ_127608,RMVar_hsa_circ_160664,RMVar_hsa_circ_92416,RMVar_hsa_circ_108704,RMVar_hsa_circ_160666,RMVar_hsa_circ_160667,RMVar_hsa_circ_160665,RMVar_hsa_circ_106199,RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_127865,RMVar_hsa_circ_160669,RMVar_hsa_circ_82818,RMVar_hsa_circ_120532,RMVar_hsa_circ_94252,RMVar_hsa_circ_160670,RMVar_hsa_circ_124983,RMVar_hsa_circ_160671,RMVar_hsa_circ_110406,RMVar_hsa_circ_113328,RMVar_hsa_circ_106678,RMVar_hsa_circ_160674,RMVar_hsa_circ_160676,RMVar_hsa_circ_160677,RMVar_hsa_circ_160675,RMVar_hsa_circ_160673,RMVar_hsa_circ_79544,RMVar_hsa_circ_117599,RMVar_hsa_circ_123973,RMVar_hsa_circ_160679,RMVar_hsa_circ_116765,RMVar_hsa_circ_160680,RMVar_hsa_circ_160678,RMVar_hsa_circ_160681 116136 RMVar_ID_116136 Human_SNP_ID_816366225 m1A Human chr12 + 56104686 56104686 56104686 TCTGACCACAGCCTGTGGCTGGGAAGGGAGACAGAGGCGGCGGCGGCTCAGGGGAAACGAGGCTG TCTGACCACAGCCTGTGGCTGGGAAGGGAGACTGAGGCGGCGGCGGCTCAGGGGAAACGAGGCTG A T PA2G4,AC034102.2 Ensembl:ENSG00000170515,Ensembl:ENSG00000257411 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:56104576..56104750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_35399,Human_RBP_ID_754168,Human_RBP_ID_811294,Human_RBP_ID_4231632,Human_RBP_ID_5314585,Human_RBP_ID_5461956,Human_RBP_ID_5521549,Human_RBP_ID_8786744,Human_RBP_ID_8940713,Human_RBP_ID_9279002,Human_RBP_ID_9322554,Human_RBP_ID_22437140,Human_RBP_ID_26320924,Human_RBP_ID_26768395,Human_RBP_ID_26908943,Human_RBP_ID_27836760 Human_miRNA_ID_1973295,Human_miRNA_ID_1975471,Human_miRNA_ID_3010687 RMVar_hsa_circ_95145,RMVar_hsa_circ_157157 116137 RMVar_ID_116137 Human_SNP_ID_816375618 m1A Human chr12 + 53299798 53299798 53299798 TAACGCTGCTGCTGCCGCCGCCACCCCTGTATACCCGGCACCGCATGCTCGGTCCAGAGTCCGTC TAACGCTGCTGCTGCCGCCGCCACCCCTGTATCCCCGGCACCGCATGCTCGGTCCAGAGTCCGTC A C C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:53299751..53299881 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4228501 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910 116138 RMVar_ID_116138 Human_SNP_ID_816376322 m1A Human chr12 + 52902001 52902001 52902001 TAGCTCTCGAACATGTTGTCCATGTTGCTTCGAGCCGTCTTCTGCTGCTGCAGGAGGCTCCACTT TAGCTCTCGAACATGTTGTCCATGTTGCTTCGTGCCGTCTTCTGCTGCTGCAGGAGGCTCCACTT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr12:52901951..52902050;chr12:52901953..52902036;chr12:52901951..52902040 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 116139 RMVar_ID_116139 Human_SNP_ID_816384489 m1A Human chr12 + 76030952 76030952 76030952 GGCGTTCCAGCCCTGGTCTTGCGGGCACCGAAAGTCGATCTCCTTGCCCTCTGCCATCACCACAG GGCGTTCCAGCCCTGGTCTTGCGGGCACCGAAGGTCGATCTCCTTGCCCTCTGCCATCACCACAG A G AC011611.3 Ensembl:ENSG00000257453 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:76030901..76031025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver Human_Splice_Rec_1400520 116140 RMVar_ID_116140 Human_SNP_ID_816387803 m1A Human chr12 - 50400996 50400996 50400996 CTCCACGAAAAGCAACATGTCGTCCTCTGCTCAGCCCAATCGTTCCCGCCGCCGCAACTCCAACT CTCCACGAAAAGCAACATGTCGTCCTCTGCTCGGCCCAATCGTTCCCGCCGCCGCAACTCCAACT T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:50400865..50401050 26863196 MeRIP-seq:(Medium) rs1357351173 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 9 large intestine 116141 RMVar_ID_116141 Human_SNP_ID_816387810 m1A Human chr12 - 110465199 110465199 110465199 GCCTTGTGACATTACAGAGCACCTACTGTGCCACCATGGTCCAGCACTGTGAAGCCCTCAACCGG GCCTTGTGACATTACAGAGCACCTACTGTGCCGCCATGGTCCAGCACTGTGAAGCCCTCAACCGG T C GPN3 Ensembl:ENSG00000111231 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:110465151..110465252 26863196 MeRIP-seq:(Medium) rs199875960 Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1355984,Human_RBP_ID_4200496,Human_RBP_ID_5315048,Human_RBP_ID_9279206,Human_RBP_ID_22438030 Human_Splice_Rec_1423246,Human_Splice_Rec_1423247,Human_Splice_Rec_1423260,Human_Splice_Rec_1423261,Human_Splice_Rec_1423274,Human_Splice_Rec_1423275,Human_Splice_Rec_1423298,Human_Splice_Rec_1423299,Human_Splice_Rec_1423308,Human_Splice_Rec_1423309,Human_Splice_Rec_1423312,Human_Splice_Rec_1423316 116142 RMVar_ID_116142 Human_SNP_ID_816404769 m1A Human chr12 - 6602105 6602105 6602105 GGAGGGGCCAGAGTTTGTGGAGGAGGAGGAAGAGGTGGCTCTGCGCTCAGACAGTGAGGGCAGCG GGAGGGGCCAGAGTTTGTGGAGGAGGAGGAAGTGGTGGCTCTGCGCTCAGACAGTGAGGGCAGCG T A CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6601951..6602200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_195252,Human_RBP_ID_228784,Human_RBP_ID_753405,Human_RBP_ID_810892,Human_RBP_ID_877150,Human_RBP_ID_1479512,Human_RBP_ID_6210619,Human_RBP_ID_9278903,Human_RBP_ID_22039144,Human_RBP_ID_24543044,Human_RBP_ID_26322646,Human_RBP_ID_27805257 Human_Splice_Rec_1329264,Human_Splice_Rec_1329392,Human_Splice_Rec_1329468,Human_Splice_Rec_1329544,Human_Splice_Rec_1329622,Human_Splice_Rec_1329712,Human_Splice_Rec_1329898,Human_Splice_Rec_1330004,Human_Splice_Rec_1330124,Human_Splice_Rec_1330200,Human_Splice_Rec_1330278,Human_Splice_Rec_1330378,Human_Splice_Rec_1330452,Human_Splice_Rec_1330528,Human_Splice_Rec_1330854,Human_Splice_Rec_1330978,Human_Splice_Rec_1331042,Human_Splice_Rec_1331232,Human_Splice_Rec_1331244,Human_Splice_Rec_1331250 RMVar_hsa_circ_267036,RMVar_hsa_circ_46896,RMVar_hsa_circ_85287,RMVar_hsa_circ_81148,RMVar_hsa_circ_107940,RMVar_hsa_circ_154594,RMVar_hsa_circ_154595,RMVar_hsa_circ_100472,RMVar_hsa_circ_87110,RMVar_hsa_circ_154599,RMVar_hsa_circ_154600,RMVar_hsa_circ_154602 116143 RMVar_ID_116143 Human_SNP_ID_816407980 m1A Human chr12 - 54283849 54283849 54283849 CCAAAATTTGAAGACTGATTGTTGTAATTCCCAAAATCATTGTAGCTTCCACCACCTCCAAAATT CCAAAATTTGAAGACTGATTGTTGTAATTCCCCAAATCATTGTAGCTTCCACCACCTCCAAAATT T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:54282810..54283925 26863196 MeRIP-seq:(Medium) rs554269174 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 116144 RMVar_ID_116144 Human_SNP_ID_816416369 m1A Human chr12 - 120291850 120291850 120291850 CGTAGCCAATGAGGTTTATCCGAGGCGCGATTATTGCTAATTGAAAACTTTTCCCAATACCCCGC CGTAGCCAATGAGGTTTATCCGAGGCGCGATTTTTGCTAATTGAAAACTTTTCCCAATACCCCGC T A RNU4-2 Ensembl:ENSG00000202538 snRNA exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:120291765..120291896 26863196 MeRIP-seq:(Medium) rs1429747184 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_275034,Human_RBP_ID_412244,Human_RBP_ID_1082697,Human_RBP_ID_1164998,Human_RBP_ID_1235675,Human_RBP_ID_1267411,Human_RBP_ID_1356287,Human_RBP_ID_1465876,Human_RBP_ID_1788655,Human_RBP_ID_2308952,Human_RBP_ID_3395525,Human_RBP_ID_4250797,Human_RBP_ID_5174046,Human_RBP_ID_5491005,Human_RBP_ID_5554711,Human_RBP_ID_6142029,Human_RBP_ID_8066081,Human_RBP_ID_8247494,Human_RBP_ID_8367273,Human_RBP_ID_8776965,Human_RBP_ID_9012160,Human_RBP_ID_9711730,Human_RBP_ID_11842008,Human_RBP_ID_17062416,Human_RBP_ID_17067265,Human_RBP_ID_17111892,Human_RBP_ID_17186764,Human_RBP_ID_17667688,Human_RBP_ID_17683512,Human_RBP_ID_17832092,Human_RBP_ID_18174135,Human_RBP_ID_18176675,Human_RBP_ID_18199044,Human_RBP_ID_18206234,Human_RBP_ID_18256051,Human_RBP_ID_18433666,Human_RBP_ID_18511055,Human_RBP_ID_18527550,Human_RBP_ID_18619507,Human_RBP_ID_19826335,Human_RBP_ID_22036559,Human_RBP_ID_22170528,Human_RBP_ID_22382576,Human_RBP_ID_22492448,Human_RBP_ID_22793250,Human_RBP_ID_22911151,Human_RBP_ID_23110230,Human_RBP_ID_23268431,Human_RBP_ID_23541942,Human_RBP_ID_24464261,Human_RBP_ID_24551380,Human_RBP_ID_24938342,Human_RBP_ID_26412651,Human_RBP_ID_26609009,Human_RBP_ID_26747946,Human_RBP_ID_26901995,Human_RBP_ID_27210753,Human_RBP_ID_27419038,Human_RBP_ID_27623673 Human_miRNA_ID_3136562,Human_miRNA_ID_3137748,Human_miRNA_ID_3138178 116145 RMVar_ID_116145 Human_SNP_ID_816424140 m1A Human chr12 - 79918640 79918640 79918640 ATGAACTAGCTTAGCGGCAGGAGGGTTGGAAAATAGTAGATGGACTTAAAATATATTTATGAAAT ATGAACTAGCTTAGCGGCAGGAGGGTTGGAAAGTAGTAGATGGACTTAAAATATATTTATGAAAT T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79918635..79918703 26863196 MeRIP-seq:(Medium) rs11114270 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_12044625 RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 116146 RMVar_ID_116146 Human_SNP_ID_816432983 m1A Human chr12 + 118246221 118246221 118246221 CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGAGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA CGGGGTCGCGGCCGTGGACGGGGCCGGGGCCGGGGCCGCGGAGCTCGCGGAGGCAAGGCCGAGGA A G RPS2P5 Ensembl:ENSG00000240342 Pseudogene exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:118246126..118246412 26863410 MeRIP-seq:(Medium) rs1039581962 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_17673054,Human_RBP_ID_18926339 116147 RMVar_ID_116147 Human_SNP_ID_816435742 m1A Human chr12 + 123584803 123584803 123584803 CATCTTCGAGGTGGCGGAGGGCGGCTTCCTGGACATCGACGTGGAGGTGCGGGCTAGCTGCCCGC CATCTTCGAGGTGGCGGAGGGCGGCTTCCTGGGCATCGACGTGGAGGTGCGGGCTAGCTGCCCGC A G TMED2 Ensembl:ENSG00000086598 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:123584601..123585574 32194978 MeRIP-seq:(Medium) rs1188523458 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_228507,Human_RBP_ID_413957,Human_RBP_ID_752633,Human_RBP_ID_809744,Human_RBP_ID_876655,Human_RBP_ID_1789981,Human_RBP_ID_4246404,Human_RBP_ID_6148668,Human_RBP_ID_9322824,Human_RBP_ID_9365804,Human_RBP_ID_11866138,Human_RBP_ID_22492611,Human_RBP_ID_23113417 Human_Splice_Rec_1439837,Human_Splice_Rec_1439843,Human_Splice_Rec_1439849,Human_Splice_Rec_1439855 RMVar_hsa_circ_124313,RMVar_hsa_circ_161352 116148 RMVar_ID_116148 Human_SNP_ID_816452738 m1A Human chr12 - 108785197 108785197 108785197 AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCAATGAGCCGAGATCGCGCCACTGCACTCCAGCC AGAATCGCTTGAACCTGGGTGGCGGAGGTTGCCATGAGCCGAGATCGCGCCACTGCACTCCAGCC T G SSH1 Ensembl:ENSG00000084112 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2003242 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_miRNA_ID_211381,Human_miRNA_ID_220896,Human_miRNA_ID_759432,Human_miRNA_ID_764373 116149 RMVar_ID_116149 Human_SNP_ID_816461022 m1A Human chr12 + 55728301 55728301 55728301 CACTCACGCAAAAGGCCAGCAGGAGGACGTAGAGCAAGAACTTCACACATTTCATTCCTCCTTCC CACTCACGCAAAAGGCCAGCAGGAGGACGTAGGGCAAGAACTTCACACATTTCATTCCTCCTTCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:55728276..55728375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver 116150 RMVar_ID_116150 Human_SNP_ID_816466046 m1A Human chr12 + 101877862 101877862 101877862 TCTTGGTGACCTGGTCGTCAGCCGCCTTCATTATCTCCTACGTGGTCGCCGTGCTCTCCGGGCAC TCTTGGTGACCTGGTCGTCAGCCGCCTTCATTGTCTCCTACGTGGTCGCCGTGCTCTCCGGGCAC A G DRAM1 Ensembl:ENSG00000136048 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:101877798..101877898 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus Human_RBP_ID_4247741,Human_RBP_ID_18433393 Human_Splice_Rec_1414999,Human_Splice_Rec_1415011,Human_Splice_Rec_1415017 RMVar_hsa_circ_91341,RMVar_hsa_circ_121372,RMVar_hsa_circ_101936,RMVar_hsa_circ_159311,RMVar_hsa_circ_159312,RMVar_hsa_circ_159310 116151 RMVar_ID_116151 Human_SNP_ID_816477664 m1A Human chr12 - 47797068 47797068 47797068 CCCTGGAGCGGAGGAAGAATCCACTGCTCCGAAAGGAGAGTGCGCCCCCCAGCCTCCGGCGGCGG CCCTGGAGCGGAGGAAGAATCCACTGCTCCGAGAGGAGAGTGCGCCCCCCAGCCTCCGGCGGCGG T C HDAC7 Ensembl:ENSG00000061273 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:47796996..47797082 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 20 breast Human_RBP_ID_3942825 Human_Splice_Rec_1360042,Human_Splice_Rec_1360043,Human_Splice_Rec_1360090,Human_Splice_Rec_1360091,Human_Splice_Rec_1360180,Human_Splice_Rec_1360181,Human_Splice_Rec_1360250,Human_Splice_Rec_1360251,Human_Splice_Rec_1360296,Human_Splice_Rec_1360297,Human_Splice_Rec_1360342,Human_Splice_Rec_1360343,Human_Splice_Rec_1360400,Human_Splice_Rec_1360401,Human_Splice_Rec_1360472,Human_Splice_Rec_1360473,Human_Splice_Rec_1360504,Human_Splice_Rec_1360505,Human_Splice_Rec_1360518,Human_Splice_Rec_1360528 Human_miRNA_ID_2684890 RMVar_hsa_circ_18742,RMVar_hsa_circ_362427,RMVar_hsa_circ_112146,RMVar_hsa_circ_24935,RMVar_hsa_circ_156147,RMVar_hsa_circ_156148,RMVar_hsa_circ_121539,RMVar_hsa_circ_318245,RMVar_hsa_circ_156149 116152 RMVar_ID_116152 Human_SNP_ID_816487274 m1A Human chr12 + 6538212 6538209 6538213 ACCACCAGCCCCAGCAAGAGCACAAGAGGAAGAGAGAGACCCTCACTGCTGGGGAGTCCCTGCCA ACCACCAGCCCCAGCAAGAGCACAAGAGGA____AGAGACCCTCACTGCTGGGGAGTCCCTGCCA AAGAG A GAPDH Ensembl:ENSG00000111640 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6538165..6538338 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 PAAD 1 - Human_RBP_ID_426009,Human_RBP_ID_17356890,Human_RBP_ID_17650564,Human_RBP_ID_22436213,Human_RBP_ID_27424470 RMVar_hsa_circ_154536,RMVar_hsa_circ_94221,RMVar_hsa_circ_100729,RMVar_hsa_circ_120054,RMVar_hsa_circ_154544,RMVar_hsa_circ_154549,RMVar_hsa_circ_109934,RMVar_hsa_circ_49293,RMVar_hsa_circ_154550,RMVar_hsa_circ_122873,RMVar_hsa_circ_154560,RMVar_hsa_circ_98859,RMVar_hsa_circ_154563,RMVar_hsa_circ_92138,RMVar_hsa_circ_76834,RMVar_hsa_circ_113434,RMVar_hsa_circ_154566,RMVar_hsa_circ_154567,RMVar_hsa_circ_154569 116153 RMVar_ID_116153 Human_SNP_ID_816499284 m1A Human chr12 - 6864120 6864120 6864120 ATGGAGACAATGGTGGTCACACAGTCCTCAGGAGGGGGGTCGGCTGCTGCGCTTGTGGAGCCCGG ATGGAGACAATGGTGGTCACACAGTCCTCAGGCGGGGGGTCGGCTGCTGCGCTTGTGGAGCCCGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6864070..6864222 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 4 liver 116154 RMVar_ID_116154 Human_SNP_ID_816504685 m1A Human chr12 - 120725921 120725921 120725921 TACGGATCCCCAGCGCACTCACCTCTGCGGGCAGGGCCCGAGGCCCGGGCGAGCAGCGCGGCGGC TACGGATCCCCAGCGCACTCACCTCTGCGGGCGGGGCCCGAGGCCCGGGCGAGCAGCGCGGCGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120725871..120725938 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116155 RMVar_ID_116155 Human_SNP_ID_816517392 m1A Human chr12 + 6937468 6937468 6937468 CACGCAGATCAAACAGGAGCCGGCTGAGGAGTATGAGACCCCCGAGAGCCCGGTGCCCCCAGCCC CACGCAGATCAAACAGGAGCCGGCTGAGGAGTTTGAGACCCCCGAGAGCCCGGTGCCCCCAGCCC A T ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:6937426..6937475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 KIRP 1 - Human_RBP_ID_4259616,Human_RBP_ID_12024473 Human_Splice_Rec_1333153,Human_Splice_Rec_1333171 RMVar_hsa_circ_64732 116156 RMVar_ID_116156 Human_SNP_ID_816530062 m1A Human chr12 - 110381786 110381786 110381786 CAAGAAGCAATAATCCACTTTCGGGAGGCCATACGGCTCGCACCTTGTCGCTTAGATTGTTATGA CAAGAAGCAATAATCCACTTTCGGGAGGCCATGCGGCTCGCACCTTGTCGCTTAGATTGTTATGA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:110381783..110381933 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_810723,Human_RBP_ID_5348722,Human_RBP_ID_6129881,Human_RBP_ID_11805316,Human_RBP_ID_17808895 Human_Splice_Rec_1423113,Human_Splice_Rec_1423125,Human_Splice_Rec_1423149,Human_Splice_Rec_1423155,Human_Splice_Rec_1423165 Human_miRNA_ID_2143702,Human_miRNA_ID_2143703,Human_miRNA_ID_2145233,Human_miRNA_ID_2145234,Human_miRNA_ID_2687734,Human_miRNA_ID_2687735,Human_miRNA_ID_2697471,Human_miRNA_ID_2697472,Human_miRNA_ID_2942391,Human_miRNA_ID_2942392 RMVar_hsa_circ_94210,RMVar_hsa_circ_113675,RMVar_hsa_circ_97652,RMVar_hsa_circ_159836,RMVar_hsa_circ_348195,RMVar_hsa_circ_32018,RMVar_hsa_circ_159840,RMVar_hsa_circ_159838,RMVar_hsa_circ_159839,RMVar_hsa_circ_60766,RMVar_hsa_circ_373418,RMVar_hsa_circ_282619,RMVar_hsa_circ_334091,RMVar_hsa_circ_337009,RMVar_hsa_circ_350663,RMVar_hsa_circ_313132,RMVar_hsa_circ_275229,RMVar_hsa_circ_159842,RMVar_hsa_circ_159844,RMVar_hsa_circ_159845,RMVar_hsa_circ_159846,RMVar_hsa_circ_159843,RMVar_hsa_circ_159841 116157 RMVar_ID_116157 Human_SNP_ID_816534054 m1A Human chr12 + 111456224 111456211 111456224 TAAATGGCTGACTGCTGCTGTGGACTGGCCAGATGGAGAGCCTGGGCGGCCTGGTGCTGATGGTG TAAATGGCTGACTGCTGCTG_____________TGGAGAGCCTGGGCGGCCTGGTGCTGATGGTG GTGGACTGGCCAGA G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:111456123..111456288 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 21..33 33 BRCA 1 - 116158 RMVar_ID_116158 Human_SNP_ID_816552395 m1A Human chr12 + 109573370 109573370 109573370 GCCACTCACCTGTCCCCGTCTTCCACGCCCTGAGGGCCGCGGCTCTGGAAACGGGGATACAGGAG GCCACTCACCTGTCCCCGTCTTCCACGCCCTGCGGGCCGCGGCTCTGGAAACGGGGATACAGGAG A C MVK Ensembl:ENSG00000110921 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:109573367..109573445 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - 116159 RMVar_ID_116159 Human_SNP_ID_816556213 m1A Human chr12 + 31613005 31613001 31613005 GAAAGAAAAAGAAAGAAAGGAAAGAAAGAGAGAAAGAAAAGAAAAGAAAAGAAGGAAAGACGGAA GAAAGAAAAAGAAAGAAAGGAAAGAAAGA____AAGAAAAGAAAAGAAAAGAAGGAAAGACGGAA AGAGA A DENND5B-AS1 Ensembl:ENSG00000255867 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31612925..31613083 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..33 33 LMS 1 - 116160 RMVar_ID_116160 Human_SNP_ID_816572098 m1A Human chr12 - 131929772 131929772 131929772 GTCATTACCAGGACGGACGCGGTCCCAGGCGCAGGGTCCACCGTCCGAAGGCTCCCAACAGCGCG GTCATTACCAGGACGGACGCGGTCCCAGGCGCCGGGTCCACCGTCCGAAGGCTCCCAACAGCGCG T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:131929722..131929898 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116161 RMVar_ID_116161 Human_SNP_ID_816581035 m1A Human chr12 - 123265264 123265264 123265264 AAGCAAATACGCGGAGCTGCTGGCCATCATTGAAGAGCTGGGGAAGGAGATCAGACCCACGTACG AAGCAAATACGCGGAGCTGCTGGCCATCATTGGAGAGCTGGGGAAGGAGATCAGACCCACGTACG T C CDK2AP1 Ensembl:ENSG00000111328 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:123261761..123265275;chr12:123265176..123265275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_413783,Human_RBP_ID_1466974,Human_RBP_ID_1789835,Human_RBP_ID_4247108,Human_RBP_ID_6148031,Human_RBP_ID_8777785,Human_RBP_ID_17236762,Human_RBP_ID_17812031,Human_RBP_ID_18620865,Human_RBP_ID_22492590,Human_RBP_ID_23125235,Human_RBP_ID_26806267 Human_Splice_Rec_1439446,Human_Splice_Rec_1439447,Human_Splice_Rec_1439478,Human_Splice_Rec_1439479,Human_Splice_Rec_1439484,Human_Splice_Rec_1439485,Human_Splice_Rec_1439490,Human_Splice_Rec_1439491,Human_Splice_Rec_1439496,Human_Splice_Rec_1439497,Human_Splice_Rec_1439500,Human_Splice_Rec_1439501,Human_Splice_Rec_1439506,Human_Splice_Rec_1439507,Human_Splice_Rec_1439512 RMVar_hsa_circ_285668 116162 RMVar_ID_116162 Human_SNP_ID_816602464 m1A Human chr12 + 31087928 31087928 31087928 TGCTGAGGGAAGACTGTTTTCTGTTCTCTCTCACACACACAGAGTGGATGAGGATGAGGATGACC TGCTGAGGGAAGACTGTTTTCTGTTCTCTCTCTCACACACAGAGTGGATGAGGATGAGGATGACC A T DDX11 Ensembl:ENSG00000013573 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31087926..31088000 26863196 MeRIP-seq:(Medium) rs7308754 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_Splice_Rec_1351875,Human_Splice_Rec_1351897,Human_Splice_Rec_1351949,Human_Splice_Rec_1351999,Human_Splice_Rec_1352017,Human_Splice_Rec_1352067,Human_Splice_Rec_1352085,Human_Splice_Rec_1352127,Human_Splice_Rec_1352177,Human_Splice_Rec_1352189,Human_Splice_Rec_1352241,Human_Splice_Rec_1352291,Human_Splice_Rec_1352313,Human_Splice_Rec_1352329,Human_Splice_Rec_1352341,Human_Splice_Rec_1352345 RMVar_hsa_circ_74755,RMVar_hsa_circ_118013,RMVar_hsa_circ_155643 116163 RMVar_ID_116163 Human_SNP_ID_816603455 m1A Human chr12 - 124989071 124989071 124989071 TGGTCTGGGAACCCACGTGGGCTGGGTTTCGGATTGCTCTGCTGGTCCGGCCGCTGGAGCGCCCA TGGTCTGGGAACCCACGTGGGCTGGGTTTCGGTTTGCTCTGCTGGTCCGGCCGCTGGAGCGCCCA T A DHX37 Ensembl:ENSG00000150990 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124988982..124989072 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_4247144,Human_RBP_ID_9365833 RMVar_hsa_circ_120739,RMVar_hsa_circ_161604 116164 RMVar_ID_116164 Human_SNP_ID_816603762 m1A Human chr12 - 121345908 121345908 121345908 GAATGGTGAGAAAAAGACAGTGGAGGATGCTGATATGGAACTGACCAGTAGAGATGAGGGTGAAA GAATGGTGAGAAAAAGACAGTGGAGGATGCTGGTATGGAACTGACCAGTAGAGATGAGGGTGAAA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:121345810..121345975 26863196 MeRIP-seq:(Medium) rs782540524 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1789036,Human_RBP_ID_3943675,Human_RBP_ID_4206423,Human_RBP_ID_8367663,Human_RBP_ID_8777248,Human_RBP_ID_11849373,Human_RBP_ID_17468694,Human_RBP_ID_18976352,Human_RBP_ID_22793311,Human_RBP_ID_23542964,Human_RBP_ID_26322167 Human_Splice_Rec_1434849,Human_Splice_Rec_1434919,Human_Splice_Rec_1434949,Human_Splice_Rec_1434977,Human_Splice_Rec_1435093,Human_Splice_Rec_1435103,Human_Splice_Rec_1435116 Human_miRNA_ID_2245603 RMVar_hsa_circ_111714,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_313313,RMVar_hsa_circ_358407,RMVar_hsa_circ_3941,RMVar_hsa_circ_36437,RMVar_hsa_circ_270470,RMVar_hsa_circ_311975,RMVar_hsa_circ_356730,RMVar_hsa_circ_160913,RMVar_hsa_circ_160914,RMVar_hsa_circ_63098,RMVar_hsa_circ_72271,RMVar_hsa_circ_106943,RMVar_hsa_circ_332100,RMVar_hsa_circ_160915 116165 RMVar_ID_116165 Human_SNP_ID_816603824 m1A Human chr12 + 52054828 52054828 52054828 CTCCTTCGGCCACTTCTCGCCCAGCCAGACTTACGAAGGCCTGCGGGCATGGACAGAGCAGCTGC CTCCTTCGGCCACTTCTCGCCCAGCCAGACTTTCGAAGGCCTGCGGGCATGGACAGAGCAGCTGC A T NR4A1 Ensembl:ENSG00000123358 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:52054779..52054927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 9 ovary Human_RBP_ID_4256131,Human_RBP_ID_27215412 Human_miRNA_ID_1966112,Human_miRNA_ID_2361570 RMVar_hsa_circ_79002,RMVar_hsa_circ_76916,RMVar_hsa_circ_156653,RMVar_hsa_circ_82671,RMVar_hsa_circ_156654,RMVar_hsa_circ_156655 116166 RMVar_ID_116166 Human_SNP_ID_816604665 m1A Human chr12 - 57089287 57089287 57089287 CCCTCCGCCCGGCGGCTGCTCGGCTGTGGGGGAAGGCGCTCTGTGCATGGACGGCCGGAGATCAC CCCTCCGCCCGGCGGCTGCTCGGCTGTGGGGGGAGGCGCTCTGTGCATGGACGGCCGGAGATCAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:57089238..57091552 32194978 MeRIP-seq:(Medium) rs889494200 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 116167 RMVar_ID_116167 Human_SNP_ID_816609407 m1A Human chr12 + 56315174 56315174 56315174 GATCCTGGCTCCTCCGAGCCCAGGCGGTTCCCAGCAGGGCCCCCAGAAGCAGGGCCAGCCAACCC GATCCTGGCTCCTCCGAGCCCAGGCGGTTCCCTGCAGGGCCCCCAGAAGCAGGGCCAGCCAACCC A T AC073896.2 Ensembl:ENSG00000257303 lincRNA exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:56315151..56315175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 116168 RMVar_ID_116168 Human_SNP_ID_816616717 m1A Human chr12 - 80103203 80103203 80103203 TCTTTCCAAAGAGCTGAGACAGAAGTACAACGAGCGATCCATGCCCATCCGAAAGGACGATGAAG TCTTTCCAAAGAGCTGAGACAGAAGTACAACGTGCGATCCATGCCCATCCGAAAGGACGATGAAG T A AC078817.1 Ensembl:ENSG00000230291 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_1478279 Human_miRNA_ID_1863744 116169 RMVar_ID_116169 Human_SNP_ID_816618113 m1A Human chr12 + 92145475 92145475 92145475 GAGCCCCTTGGTGCGGAGAAACTTGGAGATGAAGGACACGGCGGCGGCGATCTCGCCTATCATGG GAGCCCCTTGGTGCGGAGAAACTTGGAGATGAGGGACACGGCGGCGGCGATCTCGCCTATCATGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:92145426..92145825;chr12:92145426..92145850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116170 RMVar_ID_116170 Human_SNP_ID_816621656 m1A Human chr12 + 124913455 124913442 124913455 GCTGGTCAGGAGGAATGCCTTCCTTGTCCTGGATCTTTGCTTTGACGTTCTCGATGGTGTCACTG GCTGGTCAGGAGGAATGCCT_____________TCTTTGCTTTGACGTTCTCGATGGTGTCACTG TTCCTTGTCCTGGA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:124913401..124913802 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 21..33 33 BRCA 1 - 116171 RMVar_ID_116171 Human_SNP_ID_816637993 m1A Human chr12 - 111362255 111362255 111362255 AAGCAAATGCACAGTTAGTGCAGCTCCTGACCAGGCCTTCAGGGTGGACAGAGGGAGGATCGGTC AAGCAAATGCACAGTTAGTGCAGCTCCTGACCGGGCCTTCAGGGTGGACAGAGGGAGGATCGGTC T C PHETA1 Ensembl:ENSG00000198324 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10849938 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_10201,GWAS_ID_10202,GWAS_ID_10203,GWAS_ID_10204 116172 RMVar_ID_116172 Human_SNP_ID_816662607 m1A Human chr12 + 9310928 9310928 9310928 CCCCCAGGGACGCTAGTGCTGTGACATGTGTCAGAAAGGCGCAGTCAGCAGCAGCGGCTGGGTGT CCCCCAGGGACGCTAGTGCTGTGACATGTGTCGGAAAGGCGCAGTCAGCAGCAGCGGCTGGGTGT A G AC009533.1 Ensembl:ENSG00000111788 Pseudogene intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs181270058 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_229540,Human_RBP_ID_8940878,Human_RBP_ID_17243528,Human_RBP_ID_23579024 RMVar_hsa_circ_107891,RMVar_hsa_circ_154842 116173 RMVar_ID_116173 Human_SNP_ID_816683075 m1A Human chr12 - 132583170 132583170 132583170 GTCTCCAGGGGCCGCCTTGCTGTGGGGCGGGGATGCGCGCGCGGGCATCTTGGCGGCCTCCTCCT GTCTCCAGGGGCCGCCTTGCTGTGGGGCGGGGTTGCGCGCGCGGGCATCTTGGCGGCCTCCTCCT T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:132583123..132583396 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 116174 RMVar_ID_116174 Human_SNP_ID_816684008 m1A Human chr12 - 21637072 21637071 21637073 ATCCAGGATTCATCCCGTGTCAACAATGGTAAAGGTAAGACAAACTACCACAAAATGTAATATGA ATCCAGGATTCATCCCGTGTCAACAATGGTA__GGTAAGACAAACTACCACAAAATGTAATATGA CTT C LDHB,AC010197.2 Ensembl:ENSG00000111716,Ensembl:ENSG00000285854 Protein coding,Protein coding exon,CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss DEL TCGA 32..33 33 BLCA 1 - Human_RBP_ID_1480106,Human_RBP_ID_1792431,Human_RBP_ID_3400866,Human_RBP_ID_4216583,Human_RBP_ID_8372667,Human_RBP_ID_9014742,Human_RBP_ID_17241448,Human_RBP_ID_18188727,Human_RBP_ID_18623867,Human_RBP_ID_22793786,Human_RBP_ID_23552145,Human_RBP_ID_26414865,Human_RBP_ID_26768363,Human_RBP_ID_26805502,Human_RBP_ID_26905098,Human_RBP_ID_27213318 Human_Splice_Rec_1345819,Human_Splice_Rec_1345871,Human_Splice_Rec_1345875,Human_Splice_Rec_1345889,Human_Splice_Rec_1345903,Human_Splice_Rec_1345917 RMVar_hsa_circ_90923,RMVar_hsa_circ_110020,RMVar_hsa_circ_113832,RMVar_hsa_circ_111943,RMVar_hsa_circ_104276,RMVar_hsa_circ_105309,RMVar_hsa_circ_94889,RMVar_hsa_circ_155226,RMVar_hsa_circ_155230,RMVar_hsa_circ_155232,RMVar_hsa_circ_84785,RMVar_hsa_circ_155233,RMVar_hsa_circ_155231,RMVar_hsa_circ_155228,RMVar_hsa_circ_155229,RMVar_hsa_circ_155227,RMVar_hsa_circ_14657,RMVar_hsa_circ_267885 116175 RMVar_ID_116175 Human_SNP_ID_816703612 m1A Human chr12 + 68764312 68764312 68764312 ACTAAGAAGTTCCCATTATTCTCTTTTTTTAGACAGTCTTGTTCTGTCGCCTGGACTAGAGTGCA ACTAAGAAGTTCCCATTATTCTCTTTTTTTAGGCAGTCTTGTTCTGTCGCCTGGACTAGAGTGCA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10878866 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_11589,GWAS_ID_11590,GWAS_ID_11591,GWAS_ID_11592,GWAS_ID_11593 116176 RMVar_ID_116176 Human_SNP_ID_816705040 m1A Human chr12 - 20438848 20438848 20438848 GGTGGAGGCAGGAGAATCGCTTGAACCTGGGAAGTGGAGGTTGCAGTGAGCCAATATCATGCCAC GGTGGAGGCAGGAGAATCGCTTGAACCTGGGACGTGGAGGTTGCAGTGAGCCAATATCATGCCAC T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:20438801..20438954 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116177 RMVar_ID_116177 Human_SNP_ID_816705041 m1A Human chr12 - 20438848 20438848 20438848 GGTGGAGGCAGGAGAATCGCTTGAACCTGGGAAGTGGAGGTTGCAGTGAGCCAATATCATGCCAC GGTGGAGGCAGGAGAATCGCTTGAACCTGGGATGTGGAGGTTGCAGTGAGCCAATATCATGCCAC T A - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:20438801..20438954 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116178 RMVar_ID_116178 Human_SNP_ID_816717564 m1A Human chr12 - 122022108 122022108 122022108 CATCTTTGGCCCGGCTCCTCGTCTCGGCTCGAACCGACCTGCCCGACATGGTTCCGGCGGGGAGA CATCTTTGGCCCGGCTCCTCGTCTCGGCTCGACCCGACCTGCCCGACATGGTTCCGGCGGGGAGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:122022007..122022107 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116179 RMVar_ID_116179 Human_SNP_ID_816725964 m1A Human chr12 - 124372230 124372230 124372230 GGAAGGCCGAGGAGCCCGTCAAGAGCGAGTGCACGGAGGAAGCCGAGGAGGGGCCGGCCAAGGGC GGAAGGCCGAGGAGCCCGTCAAGAGCGAGTGCGCGGAGGAAGCCGAGGAGGGGCCGGCCAAGGGC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:124371999..124372635;chr12:124372001..124372630;chr12:124372001..124372636 26863196 MeRIP-seq:(Medium) rs1383586344 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_35953,Human_RBP_ID_9365821,Human_RBP_ID_22532449 Human_miRNA_ID_2464983 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_324464,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_49785,RMVar_hsa_circ_376646,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520 116180 RMVar_ID_116180 Human_SNP_ID_816726968 m1A Human chr12 - 122319324 122319324 122319324 GTATTTAGGCTGCTCAAACAGCGGAAGATGCCATGCAGATAATGGAACAGATGACCAAAGAGAAG GTATTTAGGCTGCTCAAACAGCGGAAGATGCCTTGCAGATAATGGAACAGATGACCAAAGAGAAG T A CLIP1 Ensembl:ENSG00000130779 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:122319276..122319388 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_9279337,Human_RBP_ID_26322203,Human_RBP_ID_27807303 Human_Splice_Rec_1436776,Human_Splice_Rec_1436777,Human_Splice_Rec_1436816,Human_Splice_Rec_1436817,Human_Splice_Rec_1436862,Human_Splice_Rec_1436863,Human_Splice_Rec_1436910,Human_Splice_Rec_1436911,Human_Splice_Rec_1436960,Human_Splice_Rec_1436961,Human_Splice_Rec_1437006,Human_Splice_Rec_1437007,Human_Splice_Rec_1437046,Human_Splice_Rec_1437047,Human_Splice_Rec_1437108,Human_Splice_Rec_1437109,Human_Splice_Rec_1437132 Human_miRNA_ID_245364,Human_miRNA_ID_247870 RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_269181,RMVar_hsa_circ_268219,RMVar_hsa_circ_161041,RMVar_hsa_circ_360514,RMVar_hsa_circ_360846,RMVar_hsa_circ_268999,RMVar_hsa_circ_31445,RMVar_hsa_circ_161045,RMVar_hsa_circ_270063,RMVar_hsa_circ_331709,RMVar_hsa_circ_161042,RMVar_hsa_circ_12148,RMVar_hsa_circ_359262,RMVar_hsa_circ_367744,RMVar_hsa_circ_372327,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_120675,RMVar_hsa_circ_161046,RMVar_hsa_circ_161047,RMVar_hsa_circ_277449,RMVar_hsa_circ_57681,RMVar_hsa_circ_161044,RMVar_hsa_circ_357637,RMVar_hsa_circ_359646,RMVar_hsa_circ_361743,RMVar_hsa_circ_72951,RMVar_hsa_circ_350851,RMVar_hsa_circ_364249,RMVar_hsa_circ_161048,RMVar_hsa_circ_365822,RMVar_hsa_circ_361027,RMVar_hsa_circ_343482,RMVar_hsa_circ_161050,RMVar_hsa_circ_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161051,RMVar_hsa_circ_161052,RMVar_hsa_circ_45437,RMVar_hsa_circ_161049,RMVar_hsa_circ_18786 116181 RMVar_ID_116181 Human_SNP_ID_816744837 m1A Human chr12 - 114672251 114672251 114672251 TCGGAAGCCTGTTCCCTTACCCCTACACGTACATGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA TCGGAAGCCTGTTCCCTTACCCCTACACGTACTTGGCCGCAGCGGCGGCCGCCTCCTCTGCGGCA T A TBX3 Ensembl:ENSG00000135111 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:114672201..114672250 26863196 MeRIP-seq:(Medium) rs755321111 Functional Loss SNV COSMIC 33..33 33 lung undifferentiated_carcinoma 2 lung Human_RBP_ID_228939 Human_Splice_Rec_1429492,Human_Splice_Rec_1429504 RMVar_hsa_circ_105025,RMVar_hsa_circ_120687,RMVar_hsa_circ_160405,RMVar_hsa_circ_160406 116182 RMVar_ID_116182 Human_SNP_ID_816782074 m1A Human chr12 - 79543678 79543678 79543678 AGTCCGGGCCAGGAACAATGGTAATTGTGGGAAACTCAACAAAGAGTGAGTACAGCTGAAGGAGC AGTCCGGGCCAGGAACAATGGTAATTGTGGGAGACTCAACAAAGAGTGAGTACAGCTGAAGGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:79543630..79543695 26863196 MeRIP-seq:(Medium) rs1170974760 Functional Loss SNV ICGC 33..33 33 PBCA 4 - 116183 RMVar_ID_116183 Human_SNP_ID_816783499 m1A Human chr12 - 49269685 49269685 49269685 ATCTCACTTGGGTTACTGAGGTCAACTCACCAATGACTGTGGGTTCCAAGTCTACAAACACTGCC ATCTCACTTGGGTTACTGAGGTCAACTCACCAGTGACTGTGGGTTCCAAGTCTACAAACACTGCC T C AC125611.3 Ensembl:ENSG00000258232 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49269655..49269925 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas 116184 RMVar_ID_116184 Human_SNP_ID_816783556 m1A Human chr12 + 118031396 118031395 118031396 CTGTGGGATGAATCAGTCACCCCGAATCTTGGAAAAACCCCCTTCCAGGAGAGGATGGGCAGGCA CTGTGGGATGAATCAGTCACCCCGAATCTTGG_AAAACCCCCTTCCAGGAGAGGATGGGCAGGCA GA G RFC5 Ensembl:ENSG00000111445 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:118031204..118031705 32194978 MeRIP-seq:(Medium) rs1427690936 Functional Loss DEL TCGA 33..33 33 COAD 1 - Human_RBP_ID_411731,Human_RBP_ID_17357746,Human_RBP_ID_17810538,Human_RBP_ID_23207861,Human_RBP_ID_23541075 RMVar_hsa_circ_19318,RMVar_hsa_circ_21703 116185 RMVar_ID_116185 Human_SNP_ID_816790011 m1A Human chr12 - 124911942 124911942 124911942 CACCTGGTGCTCCGTCTCAGAGGTGGGATGCAAATCTTCGTGAAGACCCTGACTGGTAAGACCAT CACCTGGTGCTCCGTCTCAGAGGTGGGATGCAGATCTTCGTGAAGACCCTGACTGGTAAGACCAT T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286;GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK293T cells, from four datasets;HEK-293T cells,m1A-IP-seq - 29072297,31548705 m1A-MAP&m1A-IP-seq:(High) rs1071727 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma 15 head and neck Human_miRNA_ID_2157713 RMVar_hsa_circ_94375,RMVar_hsa_circ_95999,RMVar_hsa_circ_79961,RMVar_hsa_circ_161581,RMVar_hsa_circ_161583,RMVar_hsa_circ_92676,RMVar_hsa_circ_161582,RMVar_hsa_circ_100069,RMVar_hsa_circ_161584,RMVar_hsa_circ_161585 116186 RMVar_ID_116186 Human_SNP_ID_816796693 m1A Human chr12 + 6583305 6583305 6583305 GATCTTCTTGCTGCTGCTCATAATGGTGCCGCAGCAATTTCTCCCAGTAGTCAGGATCCACACTT GATCTTCTTGCTGCTGCTCATAATGGTGCCGCTGCAATTTCTCCCAGTAGTCAGGATCCACACTT A T AC006064.2 Ensembl:ENSG00000247853 lincRNA exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:6583176..6583442 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-positive_carcinoma 10 breast 116187 RMVar_ID_116187 Human_SNP_ID_816802589 m1A Human chr12 + 68709254 68709253 68709254 ATATTTTTCATAATAGGCTGTTAATGCCAGTGAAAAAACAGTTGTGGAAGCGTTATTTCAGAGGG ATATTTTTCATAATAGGCTGTTAATGCCAGTG_AAAAACAGTTGTGGAAGCGTTATTTCAGAGGG GA G NUP107 Ensembl:ENSG00000111581 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss DEL TCGA 33..33 33 COAD 1 - Human_Splice_Rec_1395684,Human_Splice_Rec_1395685,Human_Splice_Rec_1395738,Human_Splice_Rec_1395739,Human_Splice_Rec_1395802,Human_Splice_Rec_1395816,Human_Splice_Rec_1395817,Human_Splice_Rec_1395866,Human_Splice_Rec_1395867,Human_Splice_Rec_1395921 RMVar_hsa_circ_2520,RMVar_hsa_circ_23198,RMVar_hsa_circ_118531,RMVar_hsa_circ_330656,RMVar_hsa_circ_343933,RMVar_hsa_circ_362332,RMVar_hsa_circ_158080,RMVar_hsa_circ_332266,RMVar_hsa_circ_72746,RMVar_hsa_circ_158084,RMVar_hsa_circ_158085,RMVar_hsa_circ_158083,RMVar_hsa_circ_357365,RMVar_hsa_circ_61143,RMVar_hsa_circ_312132,RMVar_hsa_circ_312526,RMVar_hsa_circ_367426,RMVar_hsa_circ_75408,RMVar_hsa_circ_158088,RMVar_hsa_circ_22293,RMVar_hsa_circ_49647,RMVar_hsa_circ_20227,RMVar_hsa_circ_158089,RMVar_hsa_circ_56923,RMVar_hsa_circ_89094,RMVar_hsa_circ_158091,RMVar_hsa_circ_124202,RMVar_hsa_circ_324554,RMVar_hsa_circ_328440,RMVar_hsa_circ_158092,RMVar_hsa_circ_310632,RMVar_hsa_circ_158090,RMVar_hsa_circ_295013,RMVar_hsa_circ_158093,RMVar_hsa_circ_158094,RMVar_hsa_circ_158095 116188 RMVar_ID_116188 Human_SNP_ID_816818583 m1A Human chr12 - 4605024 4605024 4605024 ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTACAACTCCGCCGTGATGCAGCCCAGGCTCCACA ATTCTCCCCGGGGAACAGGGGGTAGCCCGTGTGCAACTCCGCCGTGATGCAGCCCAGGCTCCACA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr12:4604914..4605076 26863196 MeRIP-seq:(Medium) rs750221184 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116189 RMVar_ID_116189 Human_SNP_ID_816824361 m1A Human chr12 + 77065502 77065502 77065502 ATCCCCGCGCCGAGTGCCCTGGGCTGGCGGGGACCCCGCGGCGTCCGGGCAGCGCCAGCGCTCAG ATCCCCGCGCCGAGTGCCCTGGGCTGGCGGGGGCCCCGCGGCGTCCGGGCAGCGCCAGCGCTCAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:77065455..77065529 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116190 RMVar_ID_116190 Human_SNP_ID_816830715 m1A Human chr12 + 56643500 56643500 56643500 CTTCACGGGTCCTCTCACCAACACCAGCAAACACAGAGTAACCACCATGGGCTTTGGCGACATTG CTTCACGGGTCCTCTCACCAACACCAGCAAACGCAGAGTAACCACCATGGGCTTTGGCGACATTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56643395..56643624 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - 116191 RMVar_ID_116191 Human_SNP_ID_816849257 m1A Human chr12 - 82357239 82357239 82357239 AGGACAAGGCTTTGCTTTTCGAAGAAAACTGAAAATACAGCAAAGTTACAAGAAATTGCTACGGA AGGACAAGGCTTTGCTTTTCGAAGAAAACTGAGAATACAGCAAAGTTACAAGAAATTGCTACGGA T C CCDC59 Ensembl:ENSG00000133773 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney Human_RBP_ID_1478322,Human_RBP_ID_1802289,Human_RBP_ID_4246873,Human_RBP_ID_17474040,Human_RBP_ID_22039472,Human_RBP_ID_27806932 Human_Splice_Rec_1404714,Human_Splice_Rec_1404720,Human_Splice_Rec_1404728,Human_Splice_Rec_1404734,Human_Splice_Rec_1404736,Human_Splice_Rec_1404738 RMVar_hsa_circ_52074,RMVar_hsa_circ_21640 116192 RMVar_ID_116192 Human_SNP_ID_816852137 m1A Human chr12 + 49349130 49349130 49349130 CTGAGTCCCATTCGCTTTGCTGCCCAGGTGATAGTTGGCATCTATTTTGGCCTTGTGGCACTGAT CTGAGTCCCATTCGCTTTGCTGCCCAGGTGATGGTTGGCATCTATTTTGGCCTTGTGGCACTGAT A G DNAJC22 Ensembl:ENSG00000178401 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:49349027..49349139 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 stomach adenocarcinoma,OV,ovary serous_carcinoma 6 ovary,stomach Human_RBP_ID_17820522,Human_RBP_ID_23561947 116193 RMVar_ID_116193 Human_SNP_ID_816854536 m1A Human chr12 - 2888825 2888825 2888825 GACACTAAACTGAACTGTTCATGACACAAAGTATCTTAGAAAACAAATCTCGGCTGGGCCAGCAC GACACTAAACTGAACTGTTCATGACACAAAGTTTCTTAGAAAACAAATCTCGGCTGGGCCAGCAC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:2888774..2888875 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116194 RMVar_ID_116194 Human_SNP_ID_816869836 m1A Human chr12 + 6828910 6828910 6828910 GCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTACAACTACCTGCAGAGGGCCTATTACCAGGTGG GCTCCGGGACGCCTTCCGCCGTCGGGAGCCCTTCAACTACCTGCAGAGGGCCTATTACCAGGTGG A T GPR162,P3H3 Ensembl:ENSG00000250510,Ensembl:ENSG00000110811 Protein coding,Protein coding intron,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6828656..6829039 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_17685236,Human_RBP_ID_22756548 Human_Splice_Rec_1332275 116195 RMVar_ID_116195 Human_SNP_ID_816872547 m1A Human chr12 - 53295873 53295873 53295873 TGGCTTCCACATACTTGGTCTGTACCACTTTGAGCTGAGCAATGGACGTGGACAAGAACTCCACT TGGCTTCCACATACTTGGTCTGTACCACTTTGCGCTGAGCAATGGACGTGGACAAGAACTCCACT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:53295826..53296036 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116196 RMVar_ID_116196 Human_SNP_ID_816880520 m1A Human chr12 + 32744662 32744662 32744662 TTGACCCTGGGAGGTGGAGGTTGTGGTGAGCTAAGATCGTGCCATTGCACTCCAGCCTTGGCAAC TTGACCCTGGGAGGTGGAGGTTGTGGTGAGCTGAGATCGTGCCATTGCACTCCAGCCTTGGCAAC A G DNM1L Ensembl:ENSG00000087470 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_24965716 116197 RMVar_ID_116197 Human_SNP_ID_816896614 m1A Human chr12 - 48348025 48348025 48348025 GGATGGGAATCAATGAATGTACAGCTGGATGGAGCAGAGCCCCAGGTGGAAAGGGGAAGCCAGGA GGATGGGAATCAATGAATGTACAGCTGGATGGCGCAGAGCCCCAGGTGGAAAGGGGAAGCCAGGA T G ZNF641 Ensembl:ENSG00000167528 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:48347951..48350087 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_18977025 Human_Splice_Rec_1362246,Human_Splice_Rec_1362258,Human_Splice_Rec_1362268,Human_Splice_Rec_1362276,Human_Splice_Rec_1362290,Human_Splice_Rec_1362296,Human_Splice_Rec_1362302,Human_Splice_Rec_1362308 116198 RMVar_ID_116198 Human_SNP_ID_816899320 m1A Human chr12 + 95485881 95485881 95485881 AGAAGTTAATGCTTTATTTGTATCTCACAGCAAAAGTTCAAACAGACCCTCCCTCAGTTCCAATA AGAAGTTAATGCTTTATTTGTATCTCACAGCAGAAGTTCAAACAGACCCTCCCTCAGTTCCAATA A G METAP2 Ensembl:ENSG00000111142 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr12:95485876..95485925;chr12:95485876..95485975 26863196 MeRIP-seq:(Medium) rs200917784 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_194448,Human_RBP_ID_873208,Human_RBP_ID_1479552,Human_RBP_ID_9365325,Human_RBP_ID_22539330,Human_RBP_ID_23113346,Human_RBP_ID_24543124,Human_RBP_ID_26320981,Human_RBP_ID_27805836 Human_Splice_Rec_1409166,Human_Splice_Rec_1409202,Human_Splice_Rec_1409224,Human_Splice_Rec_1409230,Human_Splice_Rec_1409240,Human_Splice_Rec_1409258,Human_Splice_Rec_1409278,Human_Splice_Rec_1409296 Human_miRNA_ID_2690215,Human_miRNA_ID_2693483 RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_17588,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_158903,RMVar_hsa_circ_358878,RMVar_hsa_circ_32493,RMVar_hsa_circ_351610,RMVar_hsa_circ_284975,RMVar_hsa_circ_314076,RMVar_hsa_circ_268859,RMVar_hsa_circ_158904 116199 RMVar_ID_116199 Human_SNP_ID_816908260 m1A Human chr12 + 48144156 48144156 48144156 CAGCAGGAAGAATGTGCTTGGTCACATGCAGCAGGTAGGGAAGACACCGTAGTCATGCCCTTCAT CAGCAGGAAGAATGTGCTTGGTCACATGCAGCTGGTAGGGAAGACACCGTAGTCATGCCCTTCAT A T PFKM Ensembl:ENSG00000152556 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48144106..48145258 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 12 lung Human_RBP_ID_3942834 Human_Splice_Rec_1361463,Human_Splice_Rec_1361515,Human_Splice_Rec_1361555,Human_Splice_Rec_1361611,Human_Splice_Rec_1361661,Human_Splice_Rec_1361731,Human_Splice_Rec_1361801,Human_Splice_Rec_1361847,Human_Splice_Rec_1361919,Human_Splice_Rec_1361969,Human_Splice_Rec_1362021,Human_Splice_Rec_1362065 RMVar_hsa_circ_60413,RMVar_hsa_circ_156180,RMVar_hsa_circ_42493 116200 RMVar_ID_116200 Human_SNP_ID_816914271 m1A Human chr12 - 122231900 122231900 122231900 GGCATGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGCCATGGTGTTTCACCATGTTGG GGCATGCACCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGCCATGGTGTTTCACCATGTTGG T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding 3'UTR,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12816400 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_11854737,Human_RBP_ID_24406565 RMVar_hsa_circ_266437 116201 RMVar_ID_116201 Human_SNP_ID_816927147 m1A Human chr12 + 52950837 52950837 52950837 CGCAAGGTCATTGATGACACCAATATCACACGACTGCAGCTGGAGACAGAGATCGAGGCTCTCAA CGCAAGGTCATTGATGACACCAATATCACACGGCTGCAGCTGGAGACAGAGATCGAGGCTCTCAA A G KRT18 Ensembl:ENSG00000111057 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:52950751..52951515 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_33862,Human_RBP_ID_810540,Human_RBP_ID_992852,Human_RBP_ID_1473260,Human_RBP_ID_1796743,Human_RBP_ID_8068474,Human_RBP_ID_8782685,Human_RBP_ID_26805662,Human_RBP_ID_27154845,Human_RBP_ID_27422854 Human_Splice_Rec_1372764,Human_Splice_Rec_1372776,Human_Splice_Rec_1372784,Human_Splice_Rec_1372798 RMVar_hsa_circ_77044,RMVar_hsa_circ_81084,RMVar_hsa_circ_97258,RMVar_hsa_circ_156785,RMVar_hsa_circ_156786,RMVar_hsa_circ_113882,RMVar_hsa_circ_156787,RMVar_hsa_circ_120985,RMVar_hsa_circ_156788,RMVar_hsa_circ_156791,RMVar_hsa_circ_111078,RMVar_hsa_circ_156790 116202 RMVar_ID_116202 Human_SNP_ID_816927533 m1A Human chr12 - 20369208 20369208 20369208 GCCCCCGCCCCGACCCACGCGCGCGCGCGCACACACACACACACACACACGCACGCACGCTCTTC GCCCCCGCCCCGACCCACGCGCGCGCGCGCACGCACACACACACACACACGCACGCACGCTCTTC T C AC129102.1 Ensembl:ENSG00000256879 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:20369171..20369273 26863196 MeRIP-seq:(Medium) rs372956905 Functional Loss SNV ICGC 33..33 33 STAD 1 - 116203 RMVar_ID_116203 Human_SNP_ID_816933907 m1A Human chr12 - 56133847 56133847 56133847 ACTCACAGGAAGATCCTGGGCCCGATCCAGGTAGACAACTAAGATGGCAGCTGACGGGGGATCTG ACTCACAGGAAGATCCTGGGCCCGATCCAGGTGGACAACTAAGATGGCAGCTGACGGGGGATCTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:56133776..56133850 32194978 MeRIP-seq:(Medium) rs1177062772 Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 116204 RMVar_ID_116204 Human_SNP_ID_816943926 m1A Human chr12 - 49997201 49997201 49997201 TCTGTTCCTTCTGCCCTGTTTTATCCCAGGTTATTAAACCTGAATCCTGTGTTCCATGTGGAAAG TCTGTTCCTTCTGCCCTGTTTTATCCCAGGTTTTTAAACCTGAATCCTGTGTTCCATGTGGAAAG T A RACGAP1 Ensembl:ENSG00000161800 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:49997151..49997225 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 7 lung Human_RBP_ID_872274,Human_RBP_ID_8782460,Human_RBP_ID_9278107,Human_RBP_ID_25016172 Human_Splice_Rec_1367158,Human_Splice_Rec_1367190,Human_Splice_Rec_1367222,Human_Splice_Rec_1367252,Human_Splice_Rec_1367288,Human_Splice_Rec_1367324,Human_Splice_Rec_1367334,Human_Splice_Rec_1367346 Human_miRNA_ID_2765619 RMVar_hsa_circ_156383,RMVar_hsa_circ_77098,RMVar_hsa_circ_125613,RMVar_hsa_circ_326702,RMVar_hsa_circ_38912,RMVar_hsa_circ_68956,RMVar_hsa_circ_156379,RMVar_hsa_circ_327659,RMVar_hsa_circ_343988,RMVar_hsa_circ_360799,RMVar_hsa_circ_336146,RMVar_hsa_circ_312022,RMVar_hsa_circ_114067,RMVar_hsa_circ_156387,RMVar_hsa_circ_75827,RMVar_hsa_circ_76367,RMVar_hsa_circ_53776,RMVar_hsa_circ_156385,RMVar_hsa_circ_156386,RMVar_hsa_circ_156384,RMVar_hsa_circ_18053,RMVar_hsa_circ_156381,RMVar_hsa_circ_156382,RMVar_hsa_circ_156380,RMVar_hsa_circ_18334,RMVar_hsa_circ_320213,RMVar_hsa_circ_334988,RMVar_hsa_circ_43019,RMVar_hsa_circ_56485,RMVar_hsa_circ_320415,RMVar_hsa_circ_82866,RMVar_hsa_circ_37187,RMVar_hsa_circ_156392 116205 RMVar_ID_116205 Human_SNP_ID_816946216 m1A Human chr12 + 53307076 53307076 53307076 CGTCCATGCAAGCGGCTTCACTGGCGGTCACCACACCCGAGAGGGTGCCTTGAGCATGGCCCGTG CGTCCATGCAAGCGGCTTCACTGGCGGTCACCGCACCCGAGAGGGTGCCTTGAGCATGGCCCGTG A G C12orf10 Ensembl:ENSG00000139637 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53307026..53307115 26863196 MeRIP-seq:(Medium) rs711316 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,central_nervous_system oligodendroglioma_Grade_III,mouth squamous_cell_carcinoma,frontal_lobe oligodendroglioma_Grade_III 11 head and neck,brain Human_RBP_ID_24365577 RMVar_hsa_circ_102362,RMVar_hsa_circ_156910,RMVar_hsa_circ_100229,RMVar_hsa_circ_109576,RMVar_hsa_circ_156912,RMVar_hsa_circ_156913 116206 RMVar_ID_116206 Human_SNP_ID_816947195 m1A Human chr12 - 71839813 71839813 71839813 AAAAGCCGAGGTCTTCCTGGAGGCCGTTACCTACCTTCCCGCTCACAACACCCGCCGCCGCCATG AAAAGCCGAGGTCTTCCTGGAGGCCGTTACCTCCCTTCCCGCTCACAACACCCGCCGCCGCCATG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:71839776..71839867;chr12:71839776..71839887 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 3 head and neck 116207 RMVar_ID_116207 Human_SNP_ID_816959378 m1A Human chr12 - 18149 18149 18149 GTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCACCTGCAGGAATATGGCTCCATCTTCACGGGCG GTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCGCCTGCAGGAATATGGCTCCATCTTCACGGGCG T C WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:18101..18184 26863196 MeRIP-seq:(Medium) rs781784246 Functional Loss SNV TCGA 33..33 33 LIHC,ESCA,KIRP,THYM 4 - Human_RBP_ID_3583,Human_RBP_ID_429335,Human_RBP_ID_872084,Human_RBP_ID_5349095,Human_RBP_ID_9365990,Human_RBP_ID_18975211,Human_RBP_ID_26321060 Human_Splice_Rec_1319482 116208 RMVar_ID_116208 Human_SNP_ID_816968722 m1A Human chr12 + 6493087 6493087 6493087 TACCAAGAGAGAAGCTTCTGCACGCCAGAGGCACCCAGTCCCACAGGCGCCTACCTGCCCCGGAT TACCAAGAGAGAAGCTTCTGCACGCCAGAGGCGCCCAGTCCCACAGGCGCCTACCTGCCCCGGAT A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6492851..6493357 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116209 RMVar_ID_116209 Human_SNP_ID_817016487 m1A Human chr12 - 98515725 98515724 98515725 GCCCGGGAAGAGCGCTGCGGAGCGGAACAAAAACTCGCGGACACAAAGCCAAGCCAGACCCGGAC GCCCGGGAAGAGCGCTGCGGAGCGGAACAAAA_CTCGCGGACACAAAGCCAAGCCAGACCCGGAC GT G TMPO-AS1 Ensembl:ENSG00000257167 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:98515601..98515900 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 COAD 1 - Human_RBP_ID_5559571 116210 RMVar_ID_116210 Human_SNP_ID_817019267 m1A Human chr12 - 57535127 57535127 57535127 TCTAGCTTGGAGAGGGTCTGGGAGTGAAGGAGACACCCCAGCAAAAGTACCAGCGCCTACTGCAT TCTAGCTTGGAGAGGGTCTGGGAGTGAAGGAGGCACCCCAGCAAAAGTACCAGCGCCTACTGCAT T C DCTN2 Ensembl:ENSG00000175203 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:57535051..57535175 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 12 oesophagus Human_RBP_ID_229290,Human_RBP_ID_754256,Human_RBP_ID_811312,Human_RBP_ID_878352,Human_RBP_ID_22572833 Human_Splice_Rec_1388788,Human_Splice_Rec_1388789,Human_Splice_Rec_1388818,Human_Splice_Rec_1388819,Human_Splice_Rec_1388844,Human_Splice_Rec_1388845,Human_Splice_Rec_1388872,Human_Splice_Rec_1388873,Human_Splice_Rec_1388891,Human_Splice_Rec_1388918,Human_Splice_Rec_1388919,Human_Splice_Rec_1388943,Human_Splice_Rec_1388956,Human_Splice_Rec_1388957,Human_Splice_Rec_1388972,Human_Splice_Rec_1388973,Human_Splice_Rec_1388998,Human_Splice_Rec_1388999,Human_Splice_Rec_1389004,Human_Splice_Rec_1389005,Human_Splice_Rec_1389014,Human_Splice_Rec_1389015,Human_Splice_Rec_1389024,Human_Splice_Rec_1389025,Human_Splice_Rec_1389030,Human_Splice_Rec_1389031,Human_Splice_Rec_1389033,Human_Splice_Rec_1389042,Human_Splice_Rec_1389048 Human_miRNA_ID_1356155,Human_miRNA_ID_2684965 RMVar_hsa_circ_84786,RMVar_hsa_circ_125355,RMVar_hsa_circ_108794,RMVar_hsa_circ_100953,RMVar_hsa_circ_102937,RMVar_hsa_circ_93357,RMVar_hsa_circ_157684,RMVar_hsa_circ_157686,RMVar_hsa_circ_157687,RMVar_hsa_circ_157685,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_14867,RMVar_hsa_circ_372411,RMVar_hsa_circ_82098,RMVar_hsa_circ_157698,RMVar_hsa_circ_157699,RMVar_hsa_circ_157700,RMVar_hsa_circ_273904 116211 RMVar_ID_116211 Human_SNP_ID_817029383 m1A Human chr12 - 120516667 120516667 120516667 TGGGAAGAAATTGCCAAAGAGTACCAGAATGAAGAAGATTCCTTGGGCGGGTCTCGTGTCGTGGT TGGGAAGAAATTGCCAAAGAGTACCAGAATGATGAAGATTCCTTGGGCGGGTCTCGTGTCGTGGT T A COQ5 Ensembl:ENSG00000110871 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120516616..120516716 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung Human_RBP_ID_17062417,Human_RBP_ID_17831171,Human_RBP_ID_23542192,Human_RBP_ID_26322158 RMVar_hsa_circ_50414,RMVar_hsa_circ_160792,RMVar_hsa_circ_356568,RMVar_hsa_circ_370482,RMVar_hsa_circ_160794,RMVar_hsa_circ_292789,RMVar_hsa_circ_294736,RMVar_hsa_circ_160795,RMVar_hsa_circ_334346,RMVar_hsa_circ_160796 116212 RMVar_ID_116212 Human_SNP_ID_817032651 m1A Human chr12 - 56724469 56724469 56724469 AACCGTCCCTGCTACAGAGCAGGAGTTGCCGCAGCCCCAGGCTGAGACAGGTAGGTTTCCCTACC AACCGTCCCTGCTACAGAGCAGGAGTTGCCGCTGCCCCAGGCTGAGACAGGTAGGTTTCCCTACC T A NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:56724451..56724550;chr12:56724451..56724525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_229479,Human_RBP_ID_424371,Human_RBP_ID_754510,Human_RBP_ID_876443,Human_RBP_ID_1474786,Human_RBP_ID_4257760,Human_RBP_ID_6202127,Human_RBP_ID_8380386,Human_RBP_ID_9018836,Human_RBP_ID_9365108,Human_RBP_ID_17239781,Human_RBP_ID_17357232,Human_RBP_ID_17475049,Human_RBP_ID_22437202,Human_RBP_ID_23582795,Human_RBP_ID_26321635,Human_RBP_ID_26909601,Human_RBP_ID_27216784 Human_Splice_Rec_1385288,Human_Splice_Rec_1385289,Human_Splice_Rec_1385308,Human_Splice_Rec_1385309,Human_Splice_Rec_1385324,Human_Splice_Rec_1385325,Human_Splice_Rec_1385340,Human_Splice_Rec_1385341,Human_Splice_Rec_1385354,Human_Splice_Rec_1385355,Human_Splice_Rec_1385368,Human_Splice_Rec_1385369,Human_Splice_Rec_1385386,Human_Splice_Rec_1385387,Human_Splice_Rec_1385400,Human_Splice_Rec_1385401,Human_Splice_Rec_1385414,Human_Splice_Rec_1385415,Human_Splice_Rec_1385426,Human_Splice_Rec_1385427,Human_Splice_Rec_1385438,Human_Splice_Rec_1385439,Human_Splice_Rec_1385446,Human_Splice_Rec_1385447,Human_Splice_Rec_1385456,Human_Splice_Rec_1385457,Human_Splice_Rec_1385468,Human_Splice_Rec_1385469,Human_Splice_Rec_1385476,Human_Splice_Rec_1385477,Human_Splice_Rec_1385482,Human_Splice_Rec_1385483,Human_Splice_Rec_1385488,Human_Splice_Rec_1385489,Human_Splice_Rec_1385494,Human_Splice_Rec_1385504,Human_Splice_Rec_1385505 RMVar_hsa_circ_83107,RMVar_hsa_circ_115300,RMVar_hsa_circ_107443,RMVar_hsa_circ_157464,RMVar_hsa_circ_157465,RMVar_hsa_circ_333170,RMVar_hsa_circ_157467,RMVar_hsa_circ_157469,RMVar_hsa_circ_374757 116213 RMVar_ID_116213 Human_SNP_ID_817057054 m1A Human chr12 - 7207700 7207700 7207700 TGAAGGCGCCGCAGCCCTTCTTCAAAAGGCTGAGGGTGATCACGCAAGGGGTTCTCCTCCTCAAA TGAAGGCGCCGCAGCCCTTCTTCAAAAGGCTGCGGGTGATCACGCAAGGGGTTCTCCTCCTCAAA T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:7203543..7207801 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine 116214 RMVar_ID_116214 Human_SNP_ID_817060373 m1A Human chr12 + 7018418 7018418 7018418 CACCACAGTCCCCTCGTCCCCCTCCGCTGAGGACGCCATCTTAACTCCGGGAGCCCCACAGGGAC CACCACAGTCCCCTCGTCCCCCTCCGCTGAGGGCGCCATCTTAACTCCGGGAGCCCCACAGGGAC A G C1S Ensembl:ENSG00000182326 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:6983436..7018465 26863196 MeRIP-seq:(Medium) rs1555157805 Functional Loss SNV TCGA 33..33 33 BRCA 1 - 116215 RMVar_ID_116215 Human_SNP_ID_817073021 m1A Human chr12 - 66129108 66129107 66129108 TTGAATGTGTGTTTTTGTTAACTTCAGGTAAAACATGGCTAAAAGCTTACGGAGTAAGTGGAAAA TTGAATGTGTGTTTTTGTTAACTTCAGGTAAA_CATGGCTAAAAGCTTACGGAGTAAGTGGAAAA GT G LLPH,AC078927.1 Ensembl:ENSG00000139233,Ensembl:ENSG00000228144 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:66129076..66129125 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - Human_RBP_ID_3411566,Human_RBP_ID_26614096 Human_Splice_Rec_1394302,Human_Splice_Rec_1394306,Human_Splice_Rec_1394320 RMVar_hsa_circ_157982,RMVar_hsa_circ_30947,RMVar_hsa_circ_357649 116216 RMVar_ID_116216 Human_SNP_ID_817082037 m1A Human chr12 + 49027223 49027206 49027223 AGGAGAAGGTGCCAAGGGGGAAGGGGGCGGGGAGGGTTCTTCAGGAGGTGGGGCCGAGAGCTGTC AGGAGAAGGTGCCAAG_________________GGGTTCTTCAGGAGGTGGGGCCGAGAGCTGTC GGGGGAAGGGGGCGGGGA G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr12:49027001..49027275 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 17..33 33 BLCA 1 - 116217 RMVar_ID_116217 Human_SNP_ID_817088839 m1A Human chr12 - 109852527 109852527 109852527 TGTAGGCATGCCCACTGCTGGACACGTCCCCGACTCGTGGCCACATGGAGAAACAGGCAAACCAG TGTAGGCATGCCCACTGCTGGACACGTCCCCGGCTCGTGGCCACATGGAGAAACAGGCAAACCAG T C GLTP Ensembl:ENSG00000139433 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:109852476..109852600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_410022,Human_RBP_ID_6128575,Human_RBP_ID_11800508 116218 RMVar_ID_116218 Human_SNP_ID_817129876 m1A Human chr12 + 6534744 6534744 6534744 GGCGCGGGCTGGGCATGGAGGCCTGGTGGGGGAGGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC GGCGCGGGCTGGGCATGGAGGCCTGGTGGGGGGGGGGAGGGGAGGCGTGTGTGTCGGCCGGGGCC A G GAPDH Ensembl:ENSG00000111640 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:6534726..6534800 26863196 MeRIP-seq:(Medium) rs1044436316 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_18934231,Human_RBP_ID_21966969,Human_RBP_ID_22645779 RMVar_hsa_circ_154536,RMVar_hsa_circ_90016,RMVar_hsa_circ_98049,RMVar_hsa_circ_122806,RMVar_hsa_circ_94221,RMVar_hsa_circ_154538,RMVar_hsa_circ_154540,RMVar_hsa_circ_77543,RMVar_hsa_circ_154539,RMVar_hsa_circ_154537 116219 RMVar_ID_116219 Human_SNP_ID_817134770 m1A Human chr12 - 123584668 123584668 123584668 AATAGCCCGAGACCGTGGCCAGGAGAGCGGCCAGAAGCACCAGCAGTTCAGCAAGCGTCACCATG AATAGCCCGAGACCGTGGCCAGGAGAGCGGCCGGAAGCACCAGCAGTTCAGCAAGCGTCACCATG T C TMED2-DT Ensembl:ENSG00000247373 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:123584541..123584858 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116220 RMVar_ID_116220 Human_SNP_ID_817143971 m1A Human chr12 - 108646093 108646093 108646093 AGAATGATAGAGAGTGAAGCAGAAACAGGAGCACAGACCTCTGCTGTAGCTTTAATGCATACAAA AGAATGATAGAGAGTGAAGCAGAAACAGGAGCGCAGACCTCTGCTGTAGCTTTAATGCATACAAA T C CORO1C Ensembl:ENSG00000110880 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2111211 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_1785964,Human_RBP_ID_6127247,Human_RBP_ID_11796778,Human_RBP_ID_17830524,Human_RBP_ID_22382377,Human_RBP_ID_23155434,Human_RBP_ID_23535262,Human_RBP_ID_26411591 Human_miRNA_ID_623897,Human_miRNA_ID_2273092 GWAS_ID_6941 RMVar_hsa_circ_159609,RMVar_hsa_circ_101388,RMVar_hsa_circ_126274,RMVar_hsa_circ_159610 116221 RMVar_ID_116221 Human_SNP_ID_817151628 m1A Human chr12 - 132664464 132664464 132664464 CAGCCCCACCCACCAGTTTGTGGTGTCCTCTCAGGGCTCGCTGGTACTCCATGGAGATGGCTGGC CAGCCCCACCCACCAGTTTGTGGTGTCCTCTCTGGGCTCGCTGGTACTCCATGGAGATGGCTGGC T A POLE Ensembl:ENSG00000177084 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:132664441..132668844 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_18417576,Human_RBP_ID_18469283 Human_Splice_Rec_1446515,Human_Splice_Rec_1446593,Human_Splice_Rec_1446691,Human_Splice_Rec_1446785,Human_Splice_Rec_1446881 RMVar_hsa_circ_161797,RMVar_hsa_circ_105170,RMVar_hsa_circ_126340,RMVar_hsa_circ_109522,RMVar_hsa_circ_89914,RMVar_hsa_circ_100002,RMVar_hsa_circ_161798,RMVar_hsa_circ_123703,RMVar_hsa_circ_161795,RMVar_hsa_circ_161796,RMVar_hsa_circ_161794,RMVar_hsa_circ_161808,RMVar_hsa_circ_106653,RMVar_hsa_circ_89786,RMVar_hsa_circ_161809,RMVar_hsa_circ_161807,RMVar_hsa_circ_127302,RMVar_hsa_circ_103276,RMVar_hsa_circ_108472,RMVar_hsa_circ_161810,RMVar_hsa_circ_161812,RMVar_hsa_circ_161811,RMVar_hsa_circ_86051,RMVar_hsa_circ_161815,RMVar_hsa_circ_106863,RMVar_hsa_circ_105628,RMVar_hsa_circ_120801,RMVar_hsa_circ_161816,RMVar_hsa_circ_111490,RMVar_hsa_circ_161817,RMVar_hsa_circ_161819,RMVar_hsa_circ_77366,RMVar_hsa_circ_96215,RMVar_hsa_circ_161820,RMVar_hsa_circ_161821,RMVar_hsa_circ_161818,RMVar_hsa_circ_85516,RMVar_hsa_circ_3208,RMVar_hsa_circ_93083,RMVar_hsa_circ_161823,RMVar_hsa_circ_95609,RMVar_hsa_circ_161826,RMVar_hsa_circ_86964,RMVar_hsa_circ_161827,RMVar_hsa_circ_161825,RMVar_hsa_circ_24861,RMVar_hsa_circ_96659,RMVar_hsa_circ_161830,RMVar_hsa_circ_107535,RMVar_hsa_circ_19661,RMVar_hsa_circ_161833,RMVar_hsa_circ_126856,RMVar_hsa_circ_161832,RMVar_hsa_circ_341755,RMVar_hsa_circ_161834,RMVar_hsa_circ_119070,RMVar_hsa_circ_161835,RMVar_hsa_circ_84478,RMVar_hsa_circ_117860,RMVar_hsa_circ_161836,RMVar_hsa_circ_161837 116222 RMVar_ID_116222 Human_SNP_ID_817171646 m1A Human chr12 - 110345368 110345368 110345368 CCGTGAAGGTGCACTAACCTGTTGAGGGCGTTACACATTTCTATAGTTACTAGAACAGAGAGCGC CCGTGAAGGTGCACTAACCTGTTGAGGGCGTTGCACATTTCTATAGTTACTAGAACAGAGAGCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:110345317..110345431 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - 116223 RMVar_ID_116223 Human_SNP_ID_817182841 m1A Human chr12 - 49051484 49051484 49051484 TCACCCCTGTTGCCACTACCTGAGGAGCCGCAACTCTGCCCCCGGTCCGAGGGGCCGCACCTGTC TCACCCCTGTTGCCACTACCTGAGGAGCCGCACCTCTGCCCCCGGTCCGAGGGGCCGCACCTGTC T G KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:49051433..49051765 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 2 breast Human_RBP_ID_754108,Human_RBP_ID_877813,Human_RBP_ID_5521519,Human_RBP_ID_9364895,Human_RBP_ID_11954265,Human_RBP_ID_17356962,Human_RBP_ID_17650634,Human_RBP_ID_17820411,Human_RBP_ID_19825920,Human_RBP_ID_22039278,Human_RBP_ID_22794204,Human_RBP_ID_23208044,Human_RBP_ID_26321411 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_102062,RMVar_hsa_circ_156275,RMVar_hsa_circ_104332,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279,RMVar_hsa_circ_156280,RMVar_hsa_circ_85177 116224 RMVar_ID_116224 Human_SNP_ID_817183153 m1A Human chr12 - 124335626 124335626 124335626 GACTCTGCACCCCCCGCCTGCCCTAGGTTACCACGGCAGCAGCTACAGCCCCGAAGGGGTGGAGC GACTCTGCACCCCCCGCCTGCCCTAGGTTACCGCGGCAGCAGCTACAGCCCCGAAGGGGTGGAGC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124335576..124335650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine Human_RBP_ID_3943824,Human_RBP_ID_4252091,Human_RBP_ID_17357440,Human_RBP_ID_18188976,Human_RBP_ID_22538992,Human_RBP_ID_22575507,Human_RBP_ID_22645592,Human_RBP_ID_22736772,Human_RBP_ID_27837063 Human_Splice_Rec_1441366,Human_Splice_Rec_1441458,Human_Splice_Rec_1441526,Human_Splice_Rec_1441596,Human_Splice_Rec_1441688 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513 116225 RMVar_ID_116225 Human_SNP_ID_817189375 m1A Human chr12 + 7210911 7210909 7210912 CTACAGAGTGTCTGGGTGTGTGGCATAGGAGGAAGGTTTGCTTGTGAAATGAGGCTGGGTGGGAG CTACAGAGTGTCTGGGTGTGTGGCATAGGAG___GGTTTGCTTGTGAAATGAGGCTGGGTGGGAG GGAA G PEX5 Ensembl:ENSG00000139197 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:7210862..7211050 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 ESCA 1 - Human_RBP_ID_428014,Human_RBP_ID_9021177,Human_RBP_ID_23574357 116226 RMVar_ID_116226 Human_SNP_ID_817190792 m1A Human chr12 - 3211856 3211856 3211856 CTCTCCAGAAGAGGAGAAGAGGAAACACAAGAAGAAACGCCTGGTGCAGAGCCCCAATTCCTACT CTCTCCAGAAGAGGAGAAGAGGAAACACAAGACGAAACGCCTGGTGCAGAGCCCCAATTCCTACT T G AC005912.1 Ensembl:ENSG00000227081 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_miRNA_ID_1855508 116227 RMVar_ID_116227 Human_SNP_ID_817197374 m1A Human chr12 - 120199391 120199390 120199391 GATGCAGCAGATCCGCATGTCCCTTCGCGGGAAGGCTGTGGTGCTGATGGGCAAGAACACCATGA GATGCAGCAGATCCGCATGTCCCTTCGCGGGA_GGCTGTGGTGCTGATGGGCAAGAACACCATGA CT C RPLP0 Ensembl:ENSG00000089157 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:120199160..120199556 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LAML 1 - Human_RBP_ID_33650,Human_RBP_ID_228550,Human_RBP_ID_412174,Human_RBP_ID_753083,Human_RBP_ID_809656,Human_RBP_ID_1164987,Human_RBP_ID_1465858,Human_RBP_ID_1788637,Human_RBP_ID_3395495,Human_RBP_ID_4247890,Human_RBP_ID_6141908,Human_RBP_ID_8367216,Human_RBP_ID_8776952,Human_RBP_ID_9012152,Human_RBP_ID_11841723,Human_RBP_ID_17236441,Human_RBP_ID_17683504,Human_RBP_ID_18188935,Human_RBP_ID_18256038,Human_RBP_ID_18619476,Human_RBP_ID_22437471,Human_RBP_ID_22492440,Human_RBP_ID_23125166,Human_RBP_ID_23541881,Human_RBP_ID_24464244,Human_RBP_ID_26807220,Human_RBP_ID_26901956,Human_RBP_ID_27210730,Human_RBP_ID_27419004 Human_Splice_Rec_1432420,Human_Splice_Rec_1432421,Human_Splice_Rec_1432434,Human_Splice_Rec_1432435,Human_Splice_Rec_1432450,Human_Splice_Rec_1432451,Human_Splice_Rec_1432462,Human_Splice_Rec_1432463,Human_Splice_Rec_1432473,Human_Splice_Rec_1432486,Human_Splice_Rec_1432487,Human_Splice_Rec_1432500,Human_Splice_Rec_1432501,Human_Splice_Rec_1432514,Human_Splice_Rec_1432515,Human_Splice_Rec_1432526,Human_Splice_Rec_1432527,Human_Splice_Rec_1432536,Human_Splice_Rec_1432537,Human_Splice_Rec_1432546,Human_Splice_Rec_1432547,Human_Splice_Rec_1432556,Human_Splice_Rec_1432557,Human_Splice_Rec_1432568,Human_Splice_Rec_1432569,Human_Splice_Rec_1432578,Human_Splice_Rec_1432579,Human_Splice_Rec_1432582,Human_Splice_Rec_1432583,Human_Splice_Rec_1432592,Human_Splice_Rec_1432593,Human_Splice_Rec_1432600,Human_Splice_Rec_1432601,Human_Splice_Rec_1432608,Human_Splice_Rec_1432609,Human_Splice_Rec_1432616,Human_Splice_Rec_1432622,Human_Splice_Rec_1432623,Human_Splice_Rec_1432628,Human_Splice_Rec_1432629,Human_Splice_Rec_1432636,Human_Splice_Rec_1432637,Human_Splice_Rec_1432642,Human_Splice_Rec_1432646,Human_Splice_Rec_1432648 Human_miRNA_ID_2056056,Human_miRNA_ID_2056057,Human_miRNA_ID_2300892,Human_miRNA_ID_2300893,Human_miRNA_ID_2304153,Human_miRNA_ID_2304154,Human_miRNA_ID_2307421,Human_miRNA_ID_2307422 RMVar_hsa_circ_92970,RMVar_hsa_circ_160753,RMVar_hsa_circ_349792,RMVar_hsa_circ_335431,RMVar_hsa_circ_101737,RMVar_hsa_circ_160760,RMVar_hsa_circ_160761,RMVar_hsa_circ_117872,RMVar_hsa_circ_373503,RMVar_hsa_circ_160763,RMVar_hsa_circ_160764,RMVar_hsa_circ_126134,RMVar_hsa_circ_127168,RMVar_hsa_circ_326074,RMVar_hsa_circ_1983,RMVar_hsa_circ_160766,RMVar_hsa_circ_160767,RMVar_hsa_circ_160769,RMVar_hsa_circ_102143,RMVar_hsa_circ_160768 116228 RMVar_ID_116228 Human_SNP_ID_817198954 m1A Human chr12 - 109915367 109915367 109915367 AGTGCCAAGAGCAAAGTCACCACCCCAAGACAAGGCCCACAGGGCAGAGCCCTGCCTCTGATGAG AGTGCCAAGAGCAAAGTCACCACCCCAAGACAGGGCCCACAGGGCAGAGCCCTGCCTCTGATGAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:109915365..109915550 26863196 MeRIP-seq:(Medium) rs3809300 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_6950,GWAS_ID_6951 116229 RMVar_ID_116229 Human_SNP_ID_817206882 m1A Human chr12 - 53299775 53299775 53299775 GGTGCCGGGTATACAGGGGTGGCGGCGGCAGCAGCAGCGTTAAGAGGCCGCGCAGGAATTGGTGT GGTGCCGGGTATACAGGGGTGGCGGCGGCAGCGGCAGCGTTAAGAGGCCGCGCAGGAATTGGTGT T C AC073611.1 Ensembl:ENSG00000257605 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:53299726..53299900 26863196 MeRIP-seq:(Medium) rs1383948298 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 116230 RMVar_ID_116230 Human_SNP_ID_817219553 m1A Human chr12 - 53461111 53461109 53461111 CTCCAACATGACCACGCAGATCTGTTTGACACACTCAATGATGGATTGTGGAATGCCAGCAATAG CTCCAACATGACCACGCAGATCTGTTTGACAC__TCAATGATGGATTGTGGAATGCCAGCAATAG AGT A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:53461061..53461174 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 HNSC 1 - 116231 RMVar_ID_116231 Human_SNP_ID_817232703 m1A Human chr12 + 110347044 110347044 110347044 TCCGTTCACCCCACCCCACCCCACCTCTCCCCACCTTACCCCCGCCCCGCTTGGCTTCTTCTTTA TCCGTTCACCCCACCCCACCCCACCTCTCCCCCCCTTACCCCCGCCCCGCTTGGCTTCTTCTTTA A C ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr12:110346944..110347195;chr12:110346994..110347179 32194978 MeRIP-seq:(Medium) rs938507310 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_229287,Human_RBP_ID_410222,Human_RBP_ID_754248,Human_RBP_ID_4249709,Human_RBP_ID_6129581,Human_RBP_ID_9661340,Human_RBP_ID_17475073,Human_RBP_ID_18934740,Human_RBP_ID_23536646,Human_RBP_ID_24406381,Human_RBP_ID_24463950 Human_miRNA_ID_446941,Human_miRNA_ID_450821,Human_miRNA_ID_842092,Human_miRNA_ID_1417992,Human_miRNA_ID_1701906,Human_miRNA_ID_2146813,Human_miRNA_ID_2367465,Human_miRNA_ID_2386948,Human_miRNA_ID_2388423,Human_miRNA_ID_2725970,Human_miRNA_ID_2988241,Human_miRNA_ID_3015260,Human_miRNA_ID_3021940,Human_miRNA_ID_3030627,Human_miRNA_ID_3065969 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_267949,RMVar_hsa_circ_100996,RMVar_hsa_circ_159835 116232 RMVar_ID_116232 Human_SNP_ID_817244884 m1A Human chr12 + 9696032 9696032 9696032 AACACCAAGATCAAAAGGACAAGAATCCTTCAAAAAACAGGAAAAATCTCCTAAAACACCAAAAG AACACCAAGATCAAAAGGACAAGAATCCTTCAGAAAACAGGAAAAATCTCCTAAAACACCAAAAG A G AC007068.1,CLEC2D Ensembl:ENSG00000213443,Ensembl:ENSG00000069493 Pseudogene,Protein coding exon,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain Human_RBP_ID_115004,Human_RBP_ID_3421991,Human_RBP_ID_5093827,Human_RBP_ID_6239591,Human_RBP_ID_17358032 Human_miRNA_ID_181272 RMVar_hsa_circ_154850 116233 RMVar_ID_116233 Human_SNP_ID_817250002 m1A Human chr12 + 57516571 57516571 57516571 GGGGAAACCCCCTGAAGCCCCTAAAGGCAAGAAGAAAAAGTAAAAGACCTTGGCTCATAGAAAGT GGGGAAACCCCCTGAAGCCCCTAAAGGCAAGAGGAAAAAGTAAAAGACCTTGGCTCATAGAAAGT A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:57516435..57516578 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach Human_RBP_ID_9365134,Human_RBP_ID_26909813 Human_Splice_Rec_1388590 Human_miRNA_ID_1744443 RMVar_hsa_circ_123367,RMVar_hsa_circ_157677 116234 RMVar_ID_116234 Human_SNP_ID_817268064 m1A Human chr12 + 6329300 6329300 6329300 GATCTCGCAGGACGGTCCTTAGAGCTGCCCGCAGGGGCGCAGCCTCATCTGAGAAGACTGGGCGC GATCTCGCAGGACGGTCCTTAGAGCTGCCCGCGGGGGCGCAGCCTCATCTGAGAAGACTGGGCGC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:6329250..6329498 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 116235 RMVar_ID_116235 Human_SNP_ID_817271870 m1A Human chr12 - 124362215 124362215 124362215 GCCAGCTCCCCCAGCCCCACCGCCACCGCAAAACCTGCAGCCGGAGAGCGACGCCCCTCAGCAGC GCCAGCTCCCCCAGCCCCACCGCCACCGCAAAGCCTGCAGCCGGAGAGCGACGCCCCTCAGCAGC T C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124362075..124362299 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_18189276 Human_Splice_Rec_1441332,Human_Splice_Rec_1441333,Human_Splice_Rec_1441424,Human_Splice_Rec_1441425,Human_Splice_Rec_1441492,Human_Splice_Rec_1441493,Human_Splice_Rec_1441562,Human_Splice_Rec_1441563,Human_Splice_Rec_1441654,Human_Splice_Rec_1441655,Human_Splice_Rec_1441800,Human_Splice_Rec_1441801 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_104619,RMVar_hsa_circ_161518,RMVar_hsa_circ_13688,RMVar_hsa_circ_287784,RMVar_hsa_circ_304932,RMVar_hsa_circ_49785,RMVar_hsa_circ_161519 116236 RMVar_ID_116236 Human_SNP_ID_817273650 m1A Human chr12 - 124335128 124335128 124335128 TGGTCACCCTGGCCCAGCACATCAGTGTAACTACGCGTTCTCTGCTGCTGCTTGTCACCTTTGCA TGGTCACCCTGGCCCAGCACATCAGTGTAACTGCGCGTTCTCTGCTGCTGCTTGTCACCTTTGCA T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:124335126..124335300 26863196 MeRIP-seq:(Medium) rs1162862210 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_19059726 RMVar_hsa_circ_94184,RMVar_hsa_circ_116623,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161507,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_88853,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_161510,RMVar_hsa_circ_161512 116237 RMVar_ID_116237 Human_SNP_ID_817273851 m1A Human chr12 + 111599164 111599164 111599164 CCGAGCGGGGAGGCGCGGGTTGGCGCGGCCGGAGGGGCGCCCGGGCTGGCGAGGGGGAGAAGGAG CCGAGCGGGGAGGCGCGGGTTGGCGCGGCCGGGGGGGCGCCCGGGCTGGCGAGGGGGAGAAGGAG A G ATXN2-AS RNACentral:URS00009C3715 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEK293T cell line,total RNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:111599019..111599332;chr12:111599045..111599311 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 6 brain 116238 RMVar_ID_116238 Human_SNP_ID_817276658 m1A Human chr12 + 6850951 6850951 6850951 CTGGTGTGACTGGGACGCTCTTGGCTGAGCCCATCTCAACCAGGAGTTGCAGGGTGGGGGCAAGG CTGGTGTGACTGGGACGCTCTTGGCTGAGCCCCTCTCAACCAGGAGTTGCAGGGTGGGGGCAAGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6850901..6851025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 116239 RMVar_ID_116239 Human_SNP_ID_817282352 m1A Human chr12 - 56688108 56688108 56688108 CCGTCGCCTGAGGGAAGCGAGAAGAGGCCGCGACCGGAGAGAAAAAGCGGAGTCGCCACCGGAGA CCGTCGCCTGAGGGAAGCGAGAAGAGGCCGCGTCCGGAGAGAAAAAGCGGAGTCGCCACCGGAGA T A PTGES3 Ensembl:ENSG00000110958 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,Wild Type;HEK293T,ALKBH3 KO chr12:56688001..56688325;chr12:56687976..56688325 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_33845,Human_RBP_ID_228651,Human_RBP_ID_811338,Human_RBP_ID_878662,Human_RBP_ID_4246155,Human_RBP_ID_8380330,Human_RBP_ID_9322579,Human_RBP_ID_9691914,Human_RBP_ID_22437852,Human_RBP_ID_22532429,Human_RBP_ID_22912551,Human_RBP_ID_25025235,Human_RBP_ID_26909563,Human_RBP_ID_27216765 RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 116240 RMVar_ID_116240 Human_SNP_ID_817298875 m1A Human chr12 + 124817601 124817601 124817601 GCTCCCGCACCTGCGGCTTCTCGCCCTTCAGGATCTCGCTGGGGTTCATGACGTCAAAGAAGTAG GCTCCCGCACCTGCGGCTTCTCGCCCTTCAGGTTCTCGCTGGGGTTCATGACGTCAAAGAAGTAG A T - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:124817551..124817625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 6 oesophagus 116241 RMVar_ID_116241 Human_SNP_ID_817312659 m1A Human chr12 + 32216388 32216388 32216388 AGATCTTGGAGATGCAGAACGAGCTGAAACAGAGCCGGGCTGTGGTCACTAATGTACAGGCAGAA AGATCTTGGAGATGCAGAACGAGCTGAAACAGGGCCGGGCTGTGGTCACTAATGTACAGGCAGAA A G BICD1 Ensembl:ENSG00000151746 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:32216342..32216439 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_26321291 Human_Splice_Rec_1352993,Human_Splice_Rec_1353013,Human_Splice_Rec_1353029 Human_miRNA_ID_1426063,Human_miRNA_ID_2055964 RMVar_hsa_circ_100488,RMVar_hsa_circ_304548,RMVar_hsa_circ_155741,RMVar_hsa_circ_64326,RMVar_hsa_circ_155742 116242 RMVar_ID_116242 Human_SNP_ID_817326883 m1A Human chr12 - 124980625 124980625 124980625 GGTGTGGGGACCACCGTGGCACCTCTGCCGCCAGCTCCAGCACCCAGCAGTCAGCCCGTGCCGGC GGTGTGGGGACCACCGTGGCACCTCTGCCGCCCGCTCCAGCACCCAGCAGTCAGCCCGTGCCGGC T G DHX37 Ensembl:ENSG00000150990 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:124980580..124980780 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_8778176 RMVar_hsa_circ_73533,RMVar_hsa_circ_120739,RMVar_hsa_circ_161604,RMVar_hsa_circ_9280,RMVar_hsa_circ_303576,RMVar_hsa_circ_313598 116243 RMVar_ID_116243 Human_SNP_ID_817333291 m1A Human chr12 + 69258665 69258665 69258665 ACCTGGTCCACCAGGTCCTCCACCTCCTGGTCAGGTTCTGCCTCCTCCTCTAGCTGGGCCTCCTA ACCTGGTCCACCAGGTCCTCCACCTCCTGGTCGGGTTCTGCCTCCTCCTCTAGCTGGGCCTCCTA A G CPSF6 Ensembl:ENSG00000111605 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:69258159..69258810 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung Human_RBP_ID_1476727,Human_RBP_ID_1800384,Human_RBP_ID_4239682,Human_RBP_ID_6214718,Human_RBP_ID_8382703,Human_RBP_ID_17474822,Human_RBP_ID_19804376,Human_RBP_ID_24557654,Human_RBP_ID_25015678,Human_RBP_ID_26321714 Human_Splice_Rec_1396500,Human_Splice_Rec_1396542,Human_Splice_Rec_1396562 Human_miRNA_ID_2475816,Human_miRNA_ID_2475817,Human_miRNA_ID_2961601,Human_miRNA_ID_2961602 RMVar_hsa_circ_158146,RMVar_hsa_circ_277579,RMVar_hsa_circ_286191,RMVar_hsa_circ_105735,RMVar_hsa_circ_158148,RMVar_hsa_circ_158147,RMVar_hsa_circ_158145,RMVar_hsa_circ_158150,RMVar_hsa_circ_334555,RMVar_hsa_circ_353172,RMVar_hsa_circ_313813,RMVar_hsa_circ_333036,RMVar_hsa_circ_271894,RMVar_hsa_circ_158151,RMVar_hsa_circ_306002 116244 RMVar_ID_116244 Human_SNP_ID_817344816 m1A Human chr12 - 52905029 52905029 52905029 CCTCACCAAGAAGCAGCTTCTCCGCTCCTTCTAGGATCTCCGCCTGGTTCGGCCCGCCTGCCTCC CCTCACCAAGAAGCAGCTTCTCCGCTCCTTCTGGGATCTCCGCCTGGTTCGGCCCGCCTGCCTCC T C KRT8 Ensembl:ENSG00000170421 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:52905026..52905075 26863196 MeRIP-seq:(Medium) rs1312169068 Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_4227790 Human_Splice_Rec_1372626 RMVar_hsa_circ_98349,RMVar_hsa_circ_114394,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769,RMVar_hsa_circ_109596,RMVar_hsa_circ_156783 116245 RMVar_ID_116245 Human_SNP_ID_817373469 m1A Human chr12 + 121822652 121822652 121822652 CCCATCTGTCCCTCCGGAGCCCCTTGCCGAGGACCACCCCCCGCATACTCCAGGCCTCTGTGGCA CCCATCTGTCCCTCCGGAGCCCCTTGCCGAGGCCCACCCCCCGCATACTCCAGGCCTCTGTGGCA A C SETD1B Ensembl:ENSG00000139718 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:121822601..121822700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 4 head and neck Human_RBP_ID_22039631,Human_RBP_ID_26322188,Human_RBP_ID_27211235,Human_RBP_ID_27419427 116246 RMVar_ID_116246 Human_SNP_ID_817376241 m1A Human chr12 + 131941622 131941621 131941623 GATCAGGGTGAAGGGCCAGAGCTTCATGATGCATCAGATCCGGAAGATGGTCGGCCTGGTGGTGG GATCAGGGTGAAGGGCCAGAGCTTCATGATGC__CAGATCCGGAAGATGGTCGGCCTGGTGGTGG CAT C PUS1 Ensembl:ENSG00000177192 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:131941572..131941901 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 SKCA 1 - Human_RBP_ID_1467998,Human_RBP_ID_1790735,Human_RBP_ID_4212700,Human_RBP_ID_9365859,Human_RBP_ID_11878579,Human_RBP_ID_17813445,Human_RBP_ID_18622050,Human_RBP_ID_22039745,Human_RBP_ID_23547960 RMVar_hsa_circ_110077,RMVar_hsa_circ_161753,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751,RMVar_hsa_circ_97965,RMVar_hsa_circ_340888,RMVar_hsa_circ_161754 116247 RMVar_ID_116247 Human_SNP_ID_817380063 m1A Human chr12 + 6915771 6915771 6915771 GCCTCCCGCCCCGCCCATTGATCTCAGGCTCCACCCCTCTAAGCCTCTTATCTTTCTCCTTCCTT GCCTCCCGCCCCGCCCATTGATCTCAGGCTCCCCCCCTCTAAGCCTCTTATCTTTCTCCTTCCTT A C ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:6915769..6915898 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_RBP_ID_5127069,Human_RBP_ID_17075035,Human_RBP_ID_22538511,Human_RBP_ID_22644601 116248 RMVar_ID_116248 Human_SNP_ID_817381581 m1A Human chr12 + 24864718 24864718 24864718 CCCATTCCAGGGAGGCGTCCATTCTCTGTCCCACTGTGCAGCAGAATTCCTCCTGACATTTATAC CCCATTCCAGGGAGGCGTCCATTCTCTGTCCCTCTGTGCAGCAGAATTCCTCCTGACATTTATAC A T - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:24864708..24864851 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116249 RMVar_ID_116249 Human_SNP_ID_817384225 m1A Human chr12 + 56714438 56714438 56714438 CTGGTTCTTCATCAATTTCAGCTGCTGCCGCCAGCTAAGAAGATAAAACAGCTATTAGTTAACCA CTGGTTCTTCATCAATTTCAGCTGCTGCCGCCGGCTAAGAAGATAAAACAGCTATTAGTTAACCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56714429..56714616 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116250 RMVar_ID_116250 Human_SNP_ID_817388218 m1A Human chr12 - 53455940 53455940 53455940 AGGCTTTGAAGATGGCATTAGTGGGTCCAGCCAAAGTGATAATTCTCTCAGGACAATTCCCTTCT AGGCTTTGAAGATGGCATTAGTGGGTCCAGCCGAAGTGATAATTCTCTCAGGACAATTCCCTTCT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:53455837..53456051 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 12 breast 116251 RMVar_ID_116251 Human_SNP_ID_817390142 m1A Human chr12 + 123459791 123459791 123459791 CCTGGGTGACAGAGTGAGACTTTGTCTCGAGTAAAAAAAGAGAATGTAAAAATCGAAAGAGATTG CCTGGGTGACAGAGTGAGACTTTGTCTCGAGTGAAAAAAGAGAATGTAAAAATCGAAAGAGATTG A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:123459786..123459918 26863196 MeRIP-seq:(Medium) rs187002924 Functional Loss SNV ICGC 33..33 33 LICA 1 - 116252 RMVar_ID_116252 Human_SNP_ID_817402140 m1A Human chr12 + 113191414 113191414 113191414 GGCCCCGCGGATGGCGAAGGGGGATGCCGCAAAGCTCCGTGCTCTCTTGTGGACGCCACCACCTA GGCCCCGCGGATGGCGAAGGGGGATGCCGCAACGCTCCGTGCTCTCTTGTGGACGCCACCACCTA A C RITA1 Ensembl:ENSG00000139405 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:113191365..113191445 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_116271 116253 RMVar_ID_116253 Human_SNP_ID_817402612 m1A Human chr12 + 56137344 56137344 56137344 GCAGTGTGGATGCCCCACCTCGACCCTGTCACACGACTCCTGATAGCCAGTTTGGGACTGAGGTG GCAGTGTGGATGCCCCACCTCGACCCTGTCACTCGACTCCTGATAGCCAGTTTGGGACTGAGGTG A T ESYT1 Ensembl:ENSG00000139641 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:56137295..56137366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_8783376,Human_RBP_ID_9255488,Human_RBP_ID_9279657 Human_Splice_Rec_1381505,Human_Splice_Rec_1381565,Human_Splice_Rec_1381607 Human_miRNA_ID_2877551,Human_miRNA_ID_2877552 RMVar_hsa_circ_75843,RMVar_hsa_circ_85928,RMVar_hsa_circ_95182,RMVar_hsa_circ_96582,RMVar_hsa_circ_157170,RMVar_hsa_circ_157171,RMVar_hsa_circ_116888,RMVar_hsa_circ_157172,RMVar_hsa_circ_157174,RMVar_hsa_circ_105977,RMVar_hsa_circ_157175,RMVar_hsa_circ_84722,RMVar_hsa_circ_157176,RMVar_hsa_circ_126519,RMVar_hsa_circ_157179,RMVar_hsa_circ_123245,RMVar_hsa_circ_157181,RMVar_hsa_circ_39757,RMVar_hsa_circ_157182,RMVar_hsa_circ_87083,RMVar_hsa_circ_373168,RMVar_hsa_circ_112911,RMVar_hsa_circ_106873,RMVar_hsa_circ_157183,RMVar_hsa_circ_157184,RMVar_hsa_circ_75755,RMVar_hsa_circ_157186,RMVar_hsa_circ_157187,RMVar_hsa_circ_121701,RMVar_hsa_circ_92390,RMVar_hsa_circ_157188,RMVar_hsa_circ_157190,RMVar_hsa_circ_157189,RMVar_hsa_circ_101332,RMVar_hsa_circ_122856,RMVar_hsa_circ_157193,RMVar_hsa_circ_157195,RMVar_hsa_circ_119482,RMVar_hsa_circ_85721,RMVar_hsa_circ_157197,RMVar_hsa_circ_17309,RMVar_hsa_circ_157196,RMVar_hsa_circ_108033,RMVar_hsa_circ_89473,RMVar_hsa_circ_123687,RMVar_hsa_circ_157198,RMVar_hsa_circ_92717,RMVar_hsa_circ_157199,RMVar_hsa_circ_157201,RMVar_hsa_circ_80348,RMVar_hsa_circ_157200,RMVar_hsa_circ_127028,RMVar_hsa_circ_329086,RMVar_hsa_circ_157202,RMVar_hsa_circ_157203,RMVar_hsa_circ_157204,RMVar_hsa_circ_104778,RMVar_hsa_circ_157205 116254 RMVar_ID_116254 Human_SNP_ID_817404469 m1A Human chr12 - 120446348 120446348 120446348 CTGTCGCCATGAACAGTGTGGGGGAGGCATGCACGGACATGAAGCGCGAGTACGACCAGTGCTTC CTGTCGCCATGAACAGTGTGGGGGAGGCATGCGCGGACATGAAGCGCGAGTACGACCAGTGCTTC T C TRIAP1 Ensembl:ENSG00000170855 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:120446198..120446400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_754195,Human_RBP_ID_4247049,Human_RBP_ID_5461479,Human_RBP_ID_6142192,Human_RBP_ID_18619539 RMVar_hsa_circ_92819,RMVar_hsa_circ_160781 116255 RMVar_ID_116255 Human_SNP_ID_817407935 m1A Human chr12 - 118035249 118035249 118035249 ATTAGCTCACTGAGATCTGTGTGCTTCTCTCCAGAAGGCTTGTACCTTGCCACGGTGGCAGATGA ATTAGCTCACTGAGATCTGTGTGCTTCTCTCCGGAAGGCTTGTACCTTGCCACGGTGGCAGATGA T C WSB2 Ensembl:ENSG00000176871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9788041 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_17810572 Human_Splice_Rec_1430962,Human_Splice_Rec_1430963,Human_Splice_Rec_1430978,Human_Splice_Rec_1430979,Human_Splice_Rec_1430994,Human_Splice_Rec_1430995,Human_Splice_Rec_1431006,Human_Splice_Rec_1431007,Human_Splice_Rec_1431020,Human_Splice_Rec_1431021,Human_Splice_Rec_1431036,Human_Splice_Rec_1431042,Human_Splice_Rec_1431043 Human_miRNA_ID_425520,Human_miRNA_ID_817483,Human_miRNA_ID_1261195,Human_miRNA_ID_1374285,Human_miRNA_ID_2136956,Human_miRNA_ID_2609599,Human_miRNA_ID_2665746,Human_miRNA_ID_2793077 GWAS_ID_10205,GWAS_ID_10206,GWAS_ID_10207,GWAS_ID_10208 RMVar_hsa_circ_14306,RMVar_hsa_circ_314695,RMVar_hsa_circ_160544,RMVar_hsa_circ_372187,RMVar_hsa_circ_26822,RMVar_hsa_circ_160545,RMVar_hsa_circ_160546,RMVar_hsa_circ_160547 116256 RMVar_ID_116256 Human_SNP_ID_817412157 m1A Human chr12 - 124355516 124355516 124355516 CATGACACTGCCCGGCCCGTCCTGCCGCGCCCACCCACCATCTCCAACCCGCCTCCCCTCATCTC CATGACACTGCCCGGCCCGTCCTGCCGCGCCCTCCCACCATCTCCAACCCGCCTCCCCTCATCTC T A NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr12:124355414..124355811;chr12:124355407..124355637 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_9255611,Human_RBP_ID_9367162,Human_RBP_ID_17357807,Human_RBP_ID_18188988,Human_RBP_ID_27419943 Human_Splice_Rec_1441336,Human_Splice_Rec_1441337,Human_Splice_Rec_1441428,Human_Splice_Rec_1441429,Human_Splice_Rec_1441496,Human_Splice_Rec_1441497,Human_Splice_Rec_1441566,Human_Splice_Rec_1441567,Human_Splice_Rec_1441658,Human_Splice_Rec_1441659,Human_Splice_Rec_1441804,Human_Splice_Rec_1441805,Human_Splice_Rec_1441822,Human_Splice_Rec_1441823,Human_Splice_Rec_1441826 Human_miRNA_ID_1984972,Human_miRNA_ID_1984973,Human_miRNA_ID_2873587,Human_miRNA_ID_2873588,Human_miRNA_ID_2940610,Human_miRNA_ID_2940611,Human_miRNA_ID_2981550,Human_miRNA_ID_2981551 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161506,RMVar_hsa_circ_86379,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_50097,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_346115,RMVar_hsa_circ_104619,RMVar_hsa_circ_25865,RMVar_hsa_circ_161518 116257 RMVar_ID_116257 Human_SNP_ID_817412490 m1A Human chr12 + 51706600 51706600 51706600 GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGAGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT GAAGAGGAAGCAAAAGGAACTCTCTGAAGGAGGGGAGAAAGGGGATCCCGAGAAGGTGTTTAAGT A G SCN8A Ensembl:ENSG00000196876 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:51706550..51706660 26863196 MeRIP-seq:(Medium) rs371383623 Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - RMVar_hsa_circ_377737,RMVar_hsa_circ_334700,RMVar_hsa_circ_6090,RMVar_hsa_circ_156618,RMVar_hsa_circ_71367,RMVar_hsa_circ_329115,RMVar_hsa_circ_329521,RMVar_hsa_circ_376897,RMVar_hsa_circ_290732,RMVar_hsa_circ_41834,RMVar_hsa_circ_91826,RMVar_hsa_circ_34336,RMVar_hsa_circ_156620,RMVar_hsa_circ_156622,RMVar_hsa_circ_156621,RMVar_hsa_circ_156619,RMVar_hsa_circ_268479,RMVar_hsa_circ_104372,RMVar_hsa_circ_156626,RMVar_hsa_circ_5823,RMVar_hsa_circ_156625,RMVar_hsa_circ_302349,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627 116258 RMVar_ID_116258 Human_SNP_ID_817414024 m1A Human chr12 - 54000682 54000682 54000682 CGGCCTTCTCCTCTTTGTGCTTGCTGCCGGCGAGCGCGTCCGCCTCGGGCGAGGGCAGTGTCTGC CGGCCTTCTCCTCTTTGTGCTTGCTGCCGGCGTGCGCGTCCGCCTCGGGCGAGGGCAGTGTCTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:54000636..54000923 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver 116259 RMVar_ID_116259 Human_SNP_ID_817420858 m1A Human chr12 + 56511652 56511652 56511652 CTGAATGATGAATTAGAAATTATTGAAGGCATAAAGTTTGATCGAGGCTATATTTCTCCATACTT CTGAATGATGAATTAGAAATTATTGAAGGCATGAAGTTTGATCGAGGCTATATTTCTCCATACTT A G HSPD1P4 Ensembl:ENSG00000257576 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs879157480 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_1063939 Human_miRNA_ID_1892910 116260 RMVar_ID_116260 Human_SNP_ID_817425933 m1A Human chr12 - 111842700 111842700 111842700 CTCAGTGGGGCCCCCACAGCCGGGAGAGGCGGAGGCTGCTCAGCAGCCCTGTCCCCGCGCGGCCG CTCAGTGGGGCCCCCACAGCCGGGAGAGGCGGCGGCTGCTCAGCAGCCCTGTCCCCGCGCGGCCG T G MAPKAPK5-AS1 Ensembl:ENSG00000234608 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr12:111842403..111842703 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 116261 RMVar_ID_116261 Human_SNP_ID_817427056 m1A Human chr12 - 31089499 31089499 31089499 CTCCAGACCACCTGCGGCTACACCATGGTCCCAGTGGCTACCGTGCCTGCTTCTCTGCATGTCCA CTCCAGACCACCTGCGGCTACACCATGGTCCCGGTGGCTACCGTGCCTGCTTCTCTGCATGTCCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:31089475..31089654 26863196 MeRIP-seq:(Medium) rs4031316 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue 116262 RMVar_ID_116262 Human_SNP_ID_817432440 m1A Human chr12 - 49128045 49128045 49128045 ATGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAAGATATGGCTGCCCTTGAGAAGGATTATGAGGA ATGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAGGATATGGCTGCCCTTGAGAAGGATTATGAGGA T C TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:49127889..49128129;chr12:49127854..49128107;chr12:49127949..49128108 26863196 MeRIP-seq:(Medium) rs747107430 Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_228881,Human_RBP_ID_420803,Human_RBP_ID_878224,Human_RBP_ID_1472603,Human_RBP_ID_4255538,Human_RBP_ID_5111439,Human_RBP_ID_5256667,Human_RBP_ID_9017657,Human_RBP_ID_9278975,Human_RBP_ID_11954538,Human_RBP_ID_17820452,Human_RBP_ID_22039304,Human_RBP_ID_22435825,Human_RBP_ID_22493316,Human_RBP_ID_22756724,Human_RBP_ID_23561775,Human_RBP_ID_26768246,Human_RBP_ID_27214908 Human_miRNA_ID_2781390,Human_miRNA_ID_2786956 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 116263 RMVar_ID_116263 Human_SNP_ID_817436928 m1A Human chr12 - 27022623 27022623 27022623 GAAAGACAGAGGCTAATCGAATGAAATTCCTCACCGAATTCACAGCGTCCTGAAGCTGCGTGAGC GAAAGACAGAGGCTAATCGAATGAAATTCCTCGCCGAATTCACAGCGTCCTGAAGCTGCGTGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:27022604..27022679 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine 116264 RMVar_ID_116264 Human_SNP_ID_817438815 m1A Human chr12 + 38823194 38823194 38823194 GTAAGTCTCTGCCTCAAGTCCCCTCAAACACTATTCTTCTATTTTAGTCTTCTTCCTTATTCTGA GTAAGTCTCTGCCTCAAGTCCCCTCAAACACTGTTCTTCTATTTTAGTCTTCTTCCTTATTCTGA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:38823191..38823314 26863196 MeRIP-seq:(Medium) rs777275506 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116265 RMVar_ID_116265 Human_SNP_ID_817451290 m1A Human chr12 + 77056064 77056064 77056064 TCTTTCTGGAGTAAATTTTTTTTGCTTCGATAAATCAATTGGTTCATTTTTTATTGGAGTCTTCG TCTTTCTGGAGTAAATTTTTTTTGCTTCGATACATCAATTGGTTCATTTTTTATTGGAGTCTTCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:77055961..77056104 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 4 lung 116266 RMVar_ID_116266 Human_SNP_ID_817451976 m1A Human chr12 + 56153974 56153974 56153974 CGTGAAGAAACCAGCAGGGCCCTCCATCTCCAAACCTGCTGCTAAGCCAGCAGCAGCAGGGGCTC CGTGAAGAAACCAGCAGGGCCCTCCATCTCCATACCTGCTGCTAAGCCAGCAGCAGCAGGGGCTC A T MYL6B Ensembl:ENSG00000196465 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:56153851..56154025 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_876930,Human_RBP_ID_1269861,Human_RBP_ID_5111486,Human_RBP_ID_5491777,Human_RBP_ID_17650736,Human_RBP_ID_18188823,Human_RBP_ID_18975731 Human_miRNA_ID_1984933,Human_miRNA_ID_2100849,Human_miRNA_ID_2106803,Human_miRNA_ID_2112745,Human_miRNA_ID_2165294,Human_miRNA_ID_2222251,Human_miRNA_ID_2485306,Human_miRNA_ID_2528538,Human_miRNA_ID_2596536,Human_miRNA_ID_2650072,Human_miRNA_ID_2652022,Human_miRNA_ID_2739449,Human_miRNA_ID_2940570,Human_miRNA_ID_3040045,Human_miRNA_ID_3073684 RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221 116267 RMVar_ID_116267 Human_SNP_ID_817458429 m1A Human chr12 - 110445488 110445478 110445489 CCAAACTCATCGGAAACATGGCACTGTTGCCTATCAGAAGTCAATTCAAAGGACCTGCCCCCAGA CCAAACTCATCGGAAACATGGCACTGTTGCC___________AATTCAAAGGACCTGCCCCCAGA TGACTTCTGATA T AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding exon,CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:110445451..110445575 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..42 33 LUSC 1 - Human_RBP_ID_36188,Human_RBP_ID_274964,Human_RBP_ID_1464004,Human_RBP_ID_1786482,Human_RBP_ID_3392534,Human_RBP_ID_4246978,Human_RBP_ID_5645389,Human_RBP_ID_17242051,Human_RBP_ID_18417334,Human_RBP_ID_18617404,Human_RBP_ID_22438027,Human_RBP_ID_26321017,Human_RBP_ID_26423122,Human_RBP_ID_26807042 Human_Splice_Rec_1423189,Human_Splice_Rec_1423198,Human_Splice_Rec_1423199,Human_Splice_Rec_1423214,Human_Splice_Rec_1423215,Human_Splice_Rec_1423227,Human_Splice_Rec_1423234,Human_Splice_Rec_1423235,Human_Splice_Rec_1423238,Human_Splice_Rec_1423239,Human_Splice_Rec_1423242,Human_Splice_Rec_1423243 RMVar_hsa_circ_357216 116268 RMVar_ID_116268 Human_SNP_ID_817459242 m1A Human chr12 - 56239522 56239522 56239522 TCCCTCTCAGCCATTTCTCACCCACTTCCCATACCCAGTGTTCATCCCCTACCTCCCCTTCCCAC TCCCTCTCAGCCATTTCTCACCCACTTCCCATGCCCAGTGTTCATCCCCTACCTCCCCTTCCCAC T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:56239471..56239605 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_423843,Human_RBP_ID_3418393,Human_RBP_ID_17823009,Human_RBP_ID_18934538,Human_RBP_ID_22421005,Human_RBP_ID_23566729 Human_miRNA_ID_2060183,Human_miRNA_ID_2185579 RMVar_hsa_circ_106953,RMVar_hsa_circ_125101,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_101351,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157273,RMVar_hsa_circ_157274,RMVar_hsa_circ_157272 116269 RMVar_ID_116269 Human_SNP_ID_817470316 m1A Human chr12 + 132632756 132632756 132632756 TCACGGGGGTGCTCCCTGGAGCACTGCGCCTCAGCCCGTCCTTCATGCAGTGGTACACGGCCACG TCACGGGGGTGCTCCCTGGAGCACTGCGCCTCCGCCCGTCCTTCATGCAGTGGTACACGGCCACG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:132632707..132632821 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 116270 RMVar_ID_116270 Human_SNP_ID_817471020 m1A Human chr12 + 1639922 1639922 1639922 CGGGAGCGAGAGAAGAACTTTGCCAAAGGATCAGAGGAGCAGGGCCGGGTGCTCATGAACCTGCA CGGGAGCGAGAGAAGAACTTTGCCAAAGGATCCGAGGAGCAGGGCCGGGTGCTCATGAACCTGCA A C WNT5B Ensembl:ENSG00000111186 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:1639871..1639963 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_1321525,Human_Splice_Rec_1321535,Human_Splice_Rec_1321543,Human_Splice_Rec_1321553 RMVar_hsa_circ_378821,RMVar_hsa_circ_7281,RMVar_hsa_circ_154270 116271 RMVar_ID_116271 Human_SNP_ID_817471993 m1A Human chr12 - 6770691 6770691 6770691 GTAGGGGAGGGAGAAAGAGAGCAAAGAGAGAGAGGAGCAATTGGGGGCCAGCTGGAGAGCTCAGA GTAGGGGAGGGAGAAAGAGAGCAAAGAGAGAGGGGAGCAATTGGGGGCCAGCTGGAGAGCTCAGA T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:6770481..6770880 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 116272 RMVar_ID_116272 Human_SNP_ID_817480577 m1A Human chr12 - 56158403 56158403 56158403 TCCTGCCCGTCTCCCAAGACCTGGGCCCCACCATCTTGACTGCTCAGCTCTCCGGGACCTTTTCC TCCTGCCCGTCTCCCAAGACCTGGGCCCCACCGTCTTGACTGCTCAGCTCTCCGGGACCTTTTCC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:56158326..56158656 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 12 skin,head and neck 116273 RMVar_ID_116273 Human_SNP_ID_817485182 m1A Human chr12 + 53454636 53454636 53454636 GTCTGACATACTGTCATTTAAGGAAAAGTGTAAAGTAGAAAATATTGATAAGGTGAAAATAACTT GTCTGACATACTGTCATTTAAGGAAAAGTGTAGAGTAGAAAATATTGATAAGGTGAAAATAACTT A G PCBP2,AC023509.1 Ensembl:ENSG00000197111,Ensembl:ENSG00000257379 Protein coding,lincRNA intron,intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr12:53454633..53454775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_1473528,Human_RBP_ID_1796962,Human_RBP_ID_9689707,Human_RBP_ID_11975236,Human_RBP_ID_17601404,Human_RBP_ID_22905223,Human_RBP_ID_24979482 RMVar_hsa_circ_82729,RMVar_hsa_circ_156946 116274 RMVar_ID_116274 Human_SNP_ID_817487267 m1A Human chr12 + 6673299 6673299 6673299 TTACAACTGTAGGGCTTAGCCCCTGAGTGTATACGGATGTGCTGGGCCAGGTAGGAGCTGTTGGC TTACAACTGTAGGGCTTAGCCCCTGAGTGTATCCGGATGTGCTGGGCCAGGTAGGAGCTGTTGGC A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:6673276..6673300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 116275 RMVar_ID_116275 Human_SNP_ID_817487600 m1A Human chr12 - 76056120 76056120 76056120 AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAAGATGAAGAAAAAGAAGACCCCAAAGGAATTCC AAAGAAAAGGCCAAGATTGAAGATGAGAAAAAGGATGAAGAAAAAGAAGACCCCAAAGGAATTCC T C NAP1L1 Ensembl:ENSG00000187109 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1059143 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_194442,Human_RBP_ID_811191,Human_RBP_ID_877958,Human_RBP_ID_1477980,Human_RBP_ID_1801678,Human_RBP_ID_2368915,Human_RBP_ID_4241894,Human_RBP_ID_6222062,Human_RBP_ID_8247862,Human_RBP_ID_8383957,Human_RBP_ID_9365251,Human_RBP_ID_17240742,Human_RBP_ID_17473808,Human_RBP_ID_18410892,Human_RBP_ID_18526788,Human_RBP_ID_18633610,Human_RBP_ID_22001529,Human_RBP_ID_22909227,Human_RBP_ID_23113344,Human_RBP_ID_23574917,Human_RBP_ID_24543107,Human_RBP_ID_25003582,Human_RBP_ID_26320975,Human_RBP_ID_26911848,Human_RBP_ID_27805738 Human_Splice_Rec_1400534,Human_Splice_Rec_1400535,Human_Splice_Rec_1400562,Human_Splice_Rec_1400563,Human_Splice_Rec_1400588,Human_Splice_Rec_1400589,Human_Splice_Rec_1400618,Human_Splice_Rec_1400619,Human_Splice_Rec_1400644,Human_Splice_Rec_1400645,Human_Splice_Rec_1400666,Human_Splice_Rec_1400667,Human_Splice_Rec_1400690,Human_Splice_Rec_1400691,Human_Splice_Rec_1400716,Human_Splice_Rec_1400717,Human_Splice_Rec_1400742,Human_Splice_Rec_1400743,Human_Splice_Rec_1400770,Human_Splice_Rec_1400771,Human_Splice_Rec_1400796,Human_Splice_Rec_1400797,Human_Splice_Rec_1400809,Human_Splice_Rec_1400840,Human_Splice_Rec_1400841,Human_Splice_Rec_1400858,Human_Splice_Rec_1400859,Human_Splice_Rec_1400878,Human_Splice_Rec_1400879,Human_Splice_Rec_1400900,Human_Splice_Rec_1400901,Human_Splice_Rec_1400918,Human_Splice_Rec_1400919,Human_Splice_Rec_1400932,Human_Splice_Rec_1400933,Human_Splice_Rec_1400948,Human_Splice_Rec_1400949,Human_Splice_Rec_1400962,Human_Splice_Rec_1400963,Human_Splice_Rec_1400970 Human_miRNA_ID_2157685,Human_miRNA_ID_2157686 GWAS_ID_6929,GWAS_ID_6930 RMVar_hsa_circ_1721,RMVar_hsa_circ_84271,RMVar_hsa_circ_158351,RMVar_hsa_circ_125050,RMVar_hsa_circ_352895,RMVar_hsa_circ_339462,RMVar_hsa_circ_357682,RMVar_hsa_circ_339015,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_158355,RMVar_hsa_circ_158356,RMVar_hsa_circ_83129,RMVar_hsa_circ_41971,RMVar_hsa_circ_158358,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_40655,RMVar_hsa_circ_158361,RMVar_hsa_circ_303154,RMVar_hsa_circ_309215,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718,RMVar_hsa_circ_367606 116276 RMVar_ID_116276 Human_SNP_ID_817494447 m1A Human chr12 + 26234510 26234510 26234510 GGCAAATGTATTGACTCACAGTGGAAACATTCATTTGGATGAAGAATTAGTGGTTTAGCCTTTGA GGCAAATGTATTGACTCACAGTGGAAACATTCGTTTGGATGAAGAATTAGTGGTTTAGCCTTTGA A G SSPN Ensembl:ENSG00000123096 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7470 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus GWAS_ID_12091,GWAS_ID_12092,GWAS_ID_12093 116277 RMVar_ID_116277 Human_SNP_ID_817495534 m1A Human chr12 - 79689788 79689788 79689788 CCAGTGCCAGGAAAGGCAAGGGGCAGATCGAGAAGAGGAAGCTGCGGGAGAAGCGGCGCTCCACC CCAGTGCCAGGAAAGGCAAGGGGCAGATCGAGGAGAGGAAGCTGCGGGAGAAGCGGCGCTCCACC T C PAWR Ensembl:ENSG00000177425 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr12:79689706..79689969 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus Human_RBP_ID_4242413 Human_Splice_Rec_1402313,Human_Splice_Rec_1402327,Human_Splice_Rec_1402333,Human_Splice_Rec_1402337,Human_Splice_Rec_1402339 RMVar_hsa_circ_63770 116278 RMVar_ID_116278 Human_SNP_ID_817512134 m1A Human chr12 - 7018394 7018394 7018394 AGATGGCGTCCTCAGCGGAGGGGGACGAGGGGACTGTGGTGGCGCTGGCGGGGGTTCTGCAGTCG AGATGGCGTCCTCAGCGGAGGGGGACGAGGGGGCTGTGGTGGCGCTGGCGGGGGTTCTGCAGTCG T C LPCAT3 Ensembl:ENSG00000111684 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr12:7018286..7018500;chr12:6983436..7018479 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 stomach adenocarcinoma,UCEC,endometrium endometrioid_carcinoma 6 uterus,stomach Human_RBP_ID_4245986,Human_RBP_ID_22436243,Human_RBP_ID_26911533 116279 RMVar_ID_116279 Human_SNP_ID_817524814 m1A Human chr12 + 6934312 6934312 6934312 TGGCAAAGCTGAGAAGTCCAGGCAGACAGCCAAGGTATTCTGTCCTCAGGTCCTCCCACAGGATG TGGCAAAGCTGAGAAGTCCAGGCAGACAGCCACGGTATTCTGTCCTCAGGTCCTCCCACAGGATG A C ATN1 Ensembl:ENSG00000111676 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:6934160..6934346 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_9364634,Human_RBP_ID_18976791,Human_RBP_ID_26321187 Human_Splice_Rec_1333149,Human_Splice_Rec_1333167 RMVar_hsa_circ_64732,RMVar_hsa_circ_305526,RMVar_hsa_circ_154661 116280 RMVar_ID_116280 Human_SNP_ID_817529715 m1A Human chr12 - 113221614 113221614 113221614 CGCATCCCTCGGATTCTTACACGCGCCGCCCCAGCAACCCGGACCGCGCGCCGGGGTCCGCACCG CGCATCCCTCGGATTCTTACACGCGCCGCCCCGGCAACCCGGACCGCGCGCCGGGGTCCGCACCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:113221517..113221630 26863410 MeRIP-seq:(Medium) rs980537022 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 116281 RMVar_ID_116281 Human_SNP_ID_817530717 m1A Human chr12 - 71663691 71663691 71663691 AGTAGGGTAAGACCGCACCGACCCAGTCCGTTAGGAAAGAAGGGAAACGAGGCAATTGTCGGGCG AGTAGGGTAAGACCGCACCGACCCAGTCCGTTGGGAAAGAAGGGAAACGAGGCAATTGTCGGGCG T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding 5'UTR GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:71663651..71663850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 6 head and neck Human_RBP_ID_3943321,Human_RBP_ID_5139906,Human_RBP_ID_5521664,Human_RBP_ID_8229919,Human_RBP_ID_18417301,Human_RBP_ID_22710087,Human_RBP_ID_25002706,Human_RBP_ID_26321730,Human_RBP_ID_27805684 116282 RMVar_ID_116282 Human_SNP_ID_817549826 m1A Human chr12 - 49044253 49044252 49044253 GCGACAGCGGAAATCCCACACACGCACGAAAAAGGGGCCTGCTGCACAGGCGGAGGTGTTGAGTG GCGACAGCGGAAATCCCACACACGCACGAAAA_GGGGCCTGCTGCACAGGCGGAGGTGTTGAGTG CT C KMT2D Ensembl:ENSG00000167548 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:49043891..49044490 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 BLCA 1 - Human_RBP_ID_6190414,Human_RBP_ID_8782204 Human_Splice_Rec_1363826,Human_Splice_Rec_1363827,Human_Splice_Rec_1363914,Human_Splice_Rec_1363915 RMVar_hsa_circ_81338,RMVar_hsa_circ_156254,RMVar_hsa_circ_78246,RMVar_hsa_circ_156253,RMVar_hsa_circ_156256,RMVar_hsa_circ_103724,RMVar_hsa_circ_87899,RMVar_hsa_circ_156257,RMVar_hsa_circ_95305,RMVar_hsa_circ_84892,RMVar_hsa_circ_87737,RMVar_hsa_circ_156258,RMVar_hsa_circ_156259,RMVar_hsa_circ_101020,RMVar_hsa_circ_156261,RMVar_hsa_circ_156262,RMVar_hsa_circ_76769,RMVar_hsa_circ_83103,RMVar_hsa_circ_90437,RMVar_hsa_circ_125307,RMVar_hsa_circ_156265,RMVar_hsa_circ_156266,RMVar_hsa_circ_107060,RMVar_hsa_circ_156267,RMVar_hsa_circ_156270,RMVar_hsa_circ_156271,RMVar_hsa_circ_114482,RMVar_hsa_circ_269263,RMVar_hsa_circ_118589,RMVar_hsa_circ_99919,RMVar_hsa_circ_156273,RMVar_hsa_circ_156274,RMVar_hsa_circ_74752,RMVar_hsa_circ_102062,RMVar_hsa_circ_107987,RMVar_hsa_circ_156275,RMVar_hsa_circ_156276,RMVar_hsa_circ_104332,RMVar_hsa_circ_156277,RMVar_hsa_circ_156278,RMVar_hsa_circ_156279 116283 RMVar_ID_116283 Human_SNP_ID_817563604 m1A Human chr12 - 48130354 48130354 48130354 CAGCCCTGACAGCAGCATTCATACCTGAAAGGAGGGACAAAAGAAGTCACGGAGAGGTTGCTCCT CAGCCCTGACAGCAGCATTCATACCTGAAAGGTGGGACAAAAGAAGTCACGGAGAGGTTGCTCCT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr12:48130351..48130400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116284 RMVar_ID_116284 Human_SNP_ID_817572806 m1A Human chr12 - 124952473 124952473 124952473 CAGGTGACCTACCTGCGACAGATCGTGACGGCAGGCCTGGGGGACCACTTGGCCCGCAGGGTCCA CAGGTGACCTACCTGCGACAGATCGTGACGGCGGGCCTGGGGGACCACTTGGCCCGCAGGGTCCA T C DHX37 Ensembl:ENSG00000150990 Protein coding exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4429156 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,mouth squamous_cell_carcinoma 11 head and neck Human_RBP_ID_229092,Human_RBP_ID_8787042 Human_Splice_Rec_1442105,Human_Splice_Rec_1442154,Human_Splice_Rec_1442155,Human_Splice_Rec_1442200,Human_Splice_Rec_1442201 RMVar_hsa_circ_97516,RMVar_hsa_circ_118039,RMVar_hsa_circ_161587,RMVar_hsa_circ_28697,RMVar_hsa_circ_107808,RMVar_hsa_circ_161589,RMVar_hsa_circ_306387,RMVar_hsa_circ_50710,RMVar_hsa_circ_161590 116285 RMVar_ID_116285 Human_SNP_ID_817577738 m1A Human chr12 - 52900682 52900682 52900682 CAGCTCAGGCTCCCCTCTCCTCATCCCCCAGGATGTGGATGAAGCTTACATGAACAAGGTAGAGC CAGCTCAGGCTCCCCTCTCCTCATCCCCCAGGGTGTGGATGAAGCTTACATGAACAAGGTAGAGC T C KRT8 Ensembl:ENSG00000170421 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr12:52900676..52900700 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_877364,Human_RBP_ID_5348336,Human_RBP_ID_9364935,Human_RBP_ID_17830292,Human_RBP_ID_19056190,Human_RBP_ID_22574556,Human_RBP_ID_23113330 Human_Splice_Rec_1372616,Human_Splice_Rec_1372617,Human_Splice_Rec_1372632,Human_Splice_Rec_1372633,Human_Splice_Rec_1372643,Human_Splice_Rec_1372655,Human_Splice_Rec_1372670,Human_Splice_Rec_1372671,Human_Splice_Rec_1372686,Human_Splice_Rec_1372687,Human_Splice_Rec_1372698,Human_Splice_Rec_1372699,Human_Splice_Rec_1372706,Human_Splice_Rec_1372707,Human_Splice_Rec_1372718,Human_Splice_Rec_1372719,Human_Splice_Rec_1372722,Human_Splice_Rec_1372723,Human_Splice_Rec_1372734,Human_Splice_Rec_1372735,Human_Splice_Rec_1372742 RMVar_hsa_circ_98349,RMVar_hsa_circ_105472,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_115919,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156774,RMVar_hsa_circ_96983,RMVar_hsa_circ_156775,RMVar_hsa_circ_156772,RMVar_hsa_circ_156773,RMVar_hsa_circ_156771,RMVar_hsa_circ_125884,RMVar_hsa_circ_156769,RMVar_hsa_circ_117415,RMVar_hsa_circ_109596,RMVar_hsa_circ_156781,RMVar_hsa_circ_156782,RMVar_hsa_circ_156783 116286 RMVar_ID_116286 Human_SNP_ID_817586963 m1A Human chr12 + 122022101 122022101 122022101 GCCTCCGTCTCCCCGCCGGAACCATGTCGGGCAGGTCGGTTCGAGCCGAGACGAGGAGCCGGGCC GCCTCCGTCTCCCCGCCGGAACCATGTCGGGCGGGTCGGTTCGAGCCGAGACGAGGAGCCGGGCC A G BCL7A Ensembl:ENSG00000110987 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr12:122022001..122022150 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4251322,Human_RBP_ID_11852505,Human_RBP_ID_19030421,Human_RBP_ID_23543357,Human_RBP_ID_26422821 Human_Splice_Rec_1436185,Human_Splice_Rec_1436195,Human_Splice_Rec_1436205 116287 RMVar_ID_116287 Human_SNP_ID_817593806 m1A Human chr12 + 50071023 50071023 50071023 GTCCTGCTCTTTTGCTCTCGGTCATTACTCATAGCTGTAGGGCCTTGAGCAGAACTGGACCCTTT GTCCTGCTCTTTTGCTCTCGGTCATTACTCATGGCTGTAGGGCCTTGAGCAGAACTGGACCCTTT A G ASIC1 Ensembl:ENSG00000110881 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr12:50071021..50071165 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_11960553 116288 RMVar_ID_116288 Human_SNP_ID_817600504 m1A Human chr12 + 57720975 57720975 57720975 AGACTCTTCCTGGACTGGCTTGCCTCCTCCCCACCTCCCCACCCTGGAACCCCTGAGGGCCAAAC AGACTCTTCCTGGACTGGCTTGCCTCCTCCCCCCCTCCCCACCCTGGAACCCCTGAGGGCCAAAC A C OS9 Ensembl:ENSG00000135506 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:57720926..57721025 32194978 MeRIP-seq:(Medium) rs867135512 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 10 liver Human_RBP_ID_228994,Human_RBP_ID_424937,Human_RBP_ID_753702,Human_RBP_ID_810465,Human_RBP_ID_876651,Human_RBP_ID_5112141,Human_RBP_ID_9366585,Human_RBP_ID_17357259,Human_RBP_ID_22436612,Human_RBP_ID_22906711,Human_RBP_ID_27424021 Human_miRNA_ID_842066,Human_miRNA_ID_1417961,Human_miRNA_ID_1701872,Human_miRNA_ID_2367445,Human_miRNA_ID_2725958,Human_miRNA_ID_2725959,Human_miRNA_ID_3015240 RMVar_hsa_circ_101715,RMVar_hsa_circ_157733 116289 RMVar_ID_116289 Human_SNP_ID_817635489 m1A Human chr12 - 124378380 124378378 124378381 CCTGATCTGCTGCTTCCCTGTGCCCCAGGAGAAGGAGAGGAACGCGCGGAGGAAGAAGAAGAAAG CCTGATCTGCTGCTTCCCTGTGCCCCAGGAG___GAGAGGAACGCGCGGAGGAAGAAGAAGAAAG CCTT C NCOR2 Ensembl:ENSG00000196498 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr12:124378376..124378400 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_5521878,Human_RBP_ID_18189279,Human_RBP_ID_24543344,Human_RBP_ID_26322335,Human_RBP_ID_27807408 Human_Splice_Rec_1441324,Human_Splice_Rec_1441418,Human_Splice_Rec_1441486,Human_Splice_Rec_1441554,Human_Splice_Rec_1441648,Human_Splice_Rec_1441792,Human_Splice_Rec_1441830 RMVar_hsa_circ_94184,RMVar_hsa_circ_105740,RMVar_hsa_circ_161505,RMVar_hsa_circ_83646,RMVar_hsa_circ_161509,RMVar_hsa_circ_161511,RMVar_hsa_circ_85806,RMVar_hsa_circ_106387,RMVar_hsa_circ_161512,RMVar_hsa_circ_161513,RMVar_hsa_circ_87619,RMVar_hsa_circ_108865,RMVar_hsa_circ_161515,RMVar_hsa_circ_161516,RMVar_hsa_circ_99896,RMVar_hsa_circ_49785,RMVar_hsa_circ_378783,RMVar_hsa_circ_55111,RMVar_hsa_circ_298116,RMVar_hsa_circ_161520,RMVar_hsa_circ_359115,RMVar_hsa_circ_6913,RMVar_hsa_circ_21997,RMVar_hsa_circ_161521 116290 RMVar_ID_116290 Human_SNP_ID_817658838 m1A Human chr12 - 66129108 66129108 66129108 TTGAATGTGTGTTTTTGTTAACTTCAGGTAAAACATGGCTAAAAGCTTACGGAGTAAGTGGAAAA TTGAATGTGTGTTTTTGTTAACTTCAGGTAAAGCATGGCTAAAAGCTTACGGAGTAAGTGGAAAA T C LLPH,AC078927.1 Ensembl:ENSG00000139233,Ensembl:ENSG00000228144 Protein coding,Protein coding 5'UTR,3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr12:66129076..66129125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_3411566,Human_RBP_ID_26614096 Human_Splice_Rec_1394302,Human_Splice_Rec_1394306,Human_Splice_Rec_1394320 RMVar_hsa_circ_157982,RMVar_hsa_circ_30947,RMVar_hsa_circ_357649 116291 RMVar_ID_116291 Human_SNP_ID_817676866 m1A Human chr12 - 57534435 57534435 57534435 CTTTTTTCATACTAGACGACAGTGAAGGAGTCAGCCACAGAGGAGAAGCTGACCCCTGTGTTGCT CTTTTTTCATACTAGACGACAGTGAAGGAGTCGGCCACAGAGGAGAAGCTGACCCCTGTGTTGCT T C DCTN2 Ensembl:ENSG00000175203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HeLa cell line,mRNA;HEK293T,ALKBH3 KO chr12:57534248..57534494;chr12:57534335..57534435 26863196,26863410 MeRIP-seq:(Medium) rs1194249747 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 3 stomach Human_RBP_ID_424814,Human_RBP_ID_874797,Human_RBP_ID_1475186,Human_RBP_ID_3941899,Human_RBP_ID_9344588,Human_RBP_ID_18977551,Human_RBP_ID_22645088,Human_RBP_ID_22794957,Human_RBP_ID_25015597,Human_RBP_ID_26321657 Human_Splice_Rec_1388790,Human_Splice_Rec_1388820,Human_Splice_Rec_1388846,Human_Splice_Rec_1388874,Human_Splice_Rec_1388892,Human_Splice_Rec_1388920,Human_Splice_Rec_1388944,Human_Splice_Rec_1388974,Human_Splice_Rec_1389006,Human_Splice_Rec_1389016,Human_Splice_Rec_1389026,Human_Splice_Rec_1389034 Human_miRNA_ID_2454156 RMVar_hsa_circ_84786,RMVar_hsa_circ_106836,RMVar_hsa_circ_125355,RMVar_hsa_circ_108794,RMVar_hsa_circ_100953,RMVar_hsa_circ_102937,RMVar_hsa_circ_93357,RMVar_hsa_circ_157684,RMVar_hsa_circ_157688,RMVar_hsa_circ_157686,RMVar_hsa_circ_157687,RMVar_hsa_circ_157685,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_48243,RMVar_hsa_circ_157697,RMVar_hsa_circ_14867,RMVar_hsa_circ_277537,RMVar_hsa_circ_372411,RMVar_hsa_circ_82098,RMVar_hsa_circ_157698,RMVar_hsa_circ_157699 116292 RMVar_ID_116292 Human_SNP_ID_817684094 m1A Human chr12 - 93641531 93641531 93641531 GATCCGGCACGGCGAGAGCGCATGGAACCTGGAGAACCGCTTCAGCGGCTGGTACGACGCCGACC GATCCGGCACGGCGAGAGCGCATGGAACCTGGGGAACCGCTTCAGCGGCTGGTACGACGCCGACC T C AC012085.1 Ensembl:ENSG00000186076 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_17357999 116293 RMVar_ID_116293 Human_SNP_ID_817685160 m1A Human chr12 + 48836736 48836736 48836736 GTCCGTCATCTCATCTAACTTTTTCTGAGACCAATGACGATCATCCCAGCGCTGCTTGGCTTCCT GTCCGTCATCTCATCTAACTTTTTCTGAGACCGATGACGATCATCCCAGCGCTGCTTGGCTTCCT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr12:48836127..48836827 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung large_cell_carcinoma,lung small_cell_carcinoma 2 lung 116294 RMVar_ID_116294 Human_SNP_ID_817686082 m1A Human chr12 - 49128077 49128077 49128077 GTGCCTTTGTTCACTGGTACGTGGGTGAGGGGATGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAA GTGCCTTTGTTCACTGGTACGTGGGTGAGGGGTTGGAGGAAGGCGAGTTTTCAGAGGCCCGTGAA T A TUBA1B Ensembl:ENSG00000123416 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr12:49128026..49128100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_228881,Human_RBP_ID_5111439,Human_RBP_ID_9278975,Human_RBP_ID_22436396,Human_RBP_ID_26768246 RMVar_hsa_circ_107269,RMVar_hsa_circ_111040,RMVar_hsa_circ_114524,RMVar_hsa_circ_156301,RMVar_hsa_circ_101417,RMVar_hsa_circ_105039,RMVar_hsa_circ_156302,RMVar_hsa_circ_156303,RMVar_hsa_circ_156299,RMVar_hsa_circ_156300 116295 RMVar_ID_116295 Human_SNP_ID_842990155 m1A Human chr21 + 33772247 33772247 33772247 GGAGCAAGAGCGCAAAAGACAACTGGAACTGGAGAAGCAACTGGAAAAGCAGCGGGAGCTAGAAC GGAGCAAGAGCGCAAAAGACAACTGGAACTGGTGAAGCAACTGGAAAAGCAGCGGGAGCTAGAAC A T ITSN1 Ensembl:ENSG00000205726 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:33772076..33772363;chr21:33772051..33772371 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_14265098 Human_Splice_Rec_2117781,Human_Splice_Rec_2117855,Human_Splice_Rec_2117913,Human_Splice_Rec_2117987,Human_Splice_Rec_2118063,Human_Splice_Rec_2118119,Human_Splice_Rec_2118173,Human_Splice_Rec_2118225,Human_Splice_Rec_2118329,Human_Splice_Rec_2118363 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_367680,RMVar_hsa_circ_42984,RMVar_hsa_circ_278358,RMVar_hsa_circ_348994,RMVar_hsa_circ_368089,RMVar_hsa_circ_323858,RMVar_hsa_circ_365529,RMVar_hsa_circ_20146,RMVar_hsa_circ_270873,RMVar_hsa_circ_54764,RMVar_hsa_circ_16760,RMVar_hsa_circ_8711,RMVar_hsa_circ_16621,RMVar_hsa_circ_49537,RMVar_hsa_circ_58634,RMVar_hsa_circ_73893,RMVar_hsa_circ_358638,RMVar_hsa_circ_332141,RMVar_hsa_circ_359046,RMVar_hsa_circ_69178,RMVar_hsa_circ_74872,RMVar_hsa_circ_366775,RMVar_hsa_circ_290243,RMVar_hsa_circ_71484,RMVar_hsa_circ_211930,RMVar_hsa_circ_29554,RMVar_hsa_circ_70784 116296 RMVar_ID_116296 Human_SNP_ID_843065255 m1A Human chr21 - 44943693 44943693 44943693 CTTGGTCCTGGCAAAGATGTTGGTGTTGATGAACGCCCAGTCCTAATGTCCCCAACAAAAACGGA CTTGGTCCTGGCAAAGATGTTGGTGTTGATGAGCGCCCAGTCCTAATGTCCCCAACAAAAACGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44940026..44943816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary 116297 RMVar_ID_116297 Human_SNP_ID_843071564 m1A Human chr21 + 45924270 45924270 45924270 ACAGTCGCGTGGATAGAAACAGCACACGTAAGATCGGGTGTGCGTGAGGAGATGCGAACACCGGG ACAGTCGCGTGGATAGAAACAGCACACGTAAGGTCGGGTGTGCGTGAGGAGATGCGAACACCGGG A G PCBP3 Ensembl:ENSG00000183570 Protein coding intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr21:45924162..45924306 26863196 MeRIP-seq:(Medium) rs1215919117 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 6 liver 116298 RMVar_ID_116298 Human_SNP_ID_843075957 m1A Human chr21 + 46334727 46334727 46334727 ACCACACACCAGAACAGCGTGGGATCTTCACAATCAGTGACCACCCAGCAGAACAGCGTGGGATG ACCACACACCAGAACAGCGTGGGATCTTCACAGTCAGTGACCACCCAGCAGAACAGCGTGGGATG A G - - Other Unknown GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs766375190 Functional Loss SNV TCGA 33..33 33 COAD 1 - 116299 RMVar_ID_116299 Human_SNP_ID_843083219 m1A Human chr21 + 44770927 44770927 44770927 GGACTCCTCATGGGGCCCACAGGGAACCAGGAAGGACCCAGAAAGGGTGCCGGGCCCTTCCCCTG GGACTCCTCATGGGGCCCACAGGGAACCAGGAGGGACCCAGAAAGGGTGCCGGGCCCTTCCCCTG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44770878..44770978 32194978 MeRIP-seq:(Medium) rs2838678 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue 116300 RMVar_ID_116300 Human_SNP_ID_843088042 m1A Human chr21 + 25905076 25905076 25905076 CGGTCGGCAGCAGGGCGGGCATCAACAGGCTCAACTGGGCACAGGAAGCAAGGGACACAGAAAGC CGGTCGGCAGCAGGGCGGGCATCAACAGGCTCTACTGGGCACAGGAAGCAAGGGACACAGAAAGC A T lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:25904963..25905133 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCS 1 - 116301 RMVar_ID_116301 Human_SNP_ID_843116751 m1A Human chr21 + 43743781 43743781 43743781 GGCCATGGTGGTGGACATTGTGCAGGAGCTGAAGCAGCAGAACCCCAGGCTGGTGTACGGTAGGC GGCCATGGTGGTGGACATTGTGCAGGAGCTGACGCAGCAGAACCCCAGGCTGGTGTACGGTAGGC A C PDXK Ensembl:ENSG00000160209 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43743684..43743846 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_64187,Human_RBP_ID_928201,Human_RBP_ID_1938033,Human_RBP_ID_3961267,Human_RBP_ID_8860040,Human_RBP_ID_17659721,Human_RBP_ID_19006733,Human_RBP_ID_19110827,Human_RBP_ID_22673092 Human_Splice_Rec_2127878,Human_Splice_Rec_2127879,Human_Splice_Rec_2127899,Human_Splice_Rec_2127914,Human_Splice_Rec_2127915,Human_Splice_Rec_2127924,Human_Splice_Rec_2127925,Human_Splice_Rec_2127946,Human_Splice_Rec_2127947,Human_Splice_Rec_2127962,Human_Splice_Rec_2127963,Human_Splice_Rec_2127978,Human_Splice_Rec_2127979,Human_Splice_Rec_2127990,Human_Splice_Rec_2127991,Human_Splice_Rec_2128006,Human_Splice_Rec_2128007,Human_Splice_Rec_2128022,Human_Splice_Rec_2128023 RMVar_hsa_circ_90856,RMVar_hsa_circ_276489,RMVar_hsa_circ_305228,RMVar_hsa_circ_315115,RMVar_hsa_circ_374028,RMVar_hsa_circ_310495,RMVar_hsa_circ_212507,RMVar_hsa_circ_212509,RMVar_hsa_circ_212508,RMVar_hsa_circ_212505,RMVar_hsa_circ_212506,RMVar_hsa_circ_114250,RMVar_hsa_circ_115153,RMVar_hsa_circ_212511,RMVar_hsa_circ_212512,RMVar_hsa_circ_119611,RMVar_hsa_circ_212513,RMVar_hsa_circ_212514 116302 RMVar_ID_116302 Human_SNP_ID_843120373 m1A Human chr21 - 43959853 43959853 43959853 CAGGGACTGGCCCAGCAGACACTCACGGCTCCAGAGTGAGTAGGCGAGGCGGCAGTTGAGGCGGC CAGGGACTGGCCCAGCAGACACTCACGGCTCCTGAGTGAGTAGGCGAGGCGGCAGTTGAGGCGGC T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:43959638..43959912 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116303 RMVar_ID_116303 Human_SNP_ID_843125668 m1A Human chr21 - 45220920 45220920 45220920 CCAGCTCATCCTTCCCAGTCGTGGCGTTGATGACCTCAATAGCGGAGTCGCCTACCGTCCAGTTG CCAGCTCATCCTTCCCAGTCGTGGCGTTGATGTCCTCAATAGCGGAGTCGCCTACCGTCCAGTTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:45220869..45220949 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 116304 RMVar_ID_116304 Human_SNP_ID_843129120 m1A Human chr21 + 33797510 33797509 33797510 GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGGAAAAAGGCAAACAGGAAGCACAAGACAAGCTGG GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGG_AAAAGGCAAACAGGAAGCACAAGACAAGCTGG GA G ITSN1 Ensembl:ENSG00000205726 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33797339..33797550 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_928089,Human_RBP_ID_5529561,Human_RBP_ID_9391449 Human_Splice_Rec_2117793,Human_Splice_Rec_2117867,Human_Splice_Rec_2117925,Human_Splice_Rec_2117999,Human_Splice_Rec_2118075,Human_Splice_Rec_2118131,Human_Splice_Rec_2118185,Human_Splice_Rec_2118237,Human_Splice_Rec_2118341,Human_Splice_Rec_2118375,Human_Splice_Rec_2118403 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_278358,RMVar_hsa_circ_8711,RMVar_hsa_circ_16621,RMVar_hsa_circ_49537,RMVar_hsa_circ_73893,RMVar_hsa_circ_366775,RMVar_hsa_circ_211930,RMVar_hsa_circ_267203,RMVar_hsa_circ_48563,RMVar_hsa_circ_211934,RMVar_hsa_circ_300094,RMVar_hsa_circ_364521,RMVar_hsa_circ_20438,RMVar_hsa_circ_211936 116305 RMVar_ID_116305 Human_SNP_ID_843143333 m1A Human chr21 - 44851629 44851629 44851629 AATGAAGTTATGATTCAAGTTTATTTTGTTTCAGGCCTGTTTAAAGAAGAAAACCCGTATGCTAG AATGAAGTTATGATTCAAGTTTATTTTGTTTCCGGCCTGTTTAAAGAAGAAAACCCGTATGCTAG T G PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44851601..44851650;chr21:44851626..44851650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_64358,Human_RBP_ID_928259,Human_RBP_ID_2706701,Human_RBP_ID_22673140,Human_RBP_ID_23930824,Human_RBP_ID_24547050 RMVar_hsa_circ_113957,RMVar_hsa_circ_123018,RMVar_hsa_circ_212605,RMVar_hsa_circ_88680,RMVar_hsa_circ_104447,RMVar_hsa_circ_212607,RMVar_hsa_circ_80161,RMVar_hsa_circ_212608,RMVar_hsa_circ_212606,RMVar_hsa_circ_212604 116306 RMVar_ID_116306 Human_SNP_ID_843157377 m1A Human chr21 + 46242864 46242864 46242864 GTCTGCAACCTGGCTTGTTCCCACGACAAAGGAACATCATATTTTTTCAAATCGTTTTTAAAAAA GTCTGCAACCTGGCTTGTTCCCACGACAAAGGGACATCATATTTTTTCAAATCGTTTTTAAAAAA A G MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:46242811..46242961 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_7053939,Human_RBP_ID_18327213 116307 RMVar_ID_116307 Human_SNP_ID_843214893 m1A Human chr21 - 33511311 33511311 33511311 ATCAAAGGAGCAGACAGAGCAGATTCTGAGGGATATCCAGCAGCACAAGGAAGAAGCCTGGGTGA ATCAAAGGAGCAGACAGAGCAGATTCTGAGGGGTATCCAGCAGCACAAGGAAGAAGCCTGGGTGA T C GART Ensembl:ENSG00000159131 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8971 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_7039758,Human_RBP_ID_14257032,Human_RBP_ID_17981411,Human_RBP_ID_19006661 Human_Splice_Rec_2116869,Human_Splice_Rec_2116911,Human_Splice_Rec_2116953,Human_Splice_Rec_2116993,Human_Splice_Rec_2117005 GWAS_ID_12592,GWAS_ID_12593,GWAS_ID_12594,GWAS_ID_12595,GWAS_ID_12596 RMVar_hsa_circ_6781,RMVar_hsa_circ_38850,RMVar_hsa_circ_20820,RMVar_hsa_circ_41605,RMVar_hsa_circ_334817,RMVar_hsa_circ_347799,RMVar_hsa_circ_24371 116308 RMVar_ID_116308 Human_SNP_ID_843234174 m1A Human chr21 - 32278827 32278827 32278827 GAGCTCCATGAGCGAAGACGCGTCGGTGGCCGACATGGAGAGGGCGCAGCTGGAGGAGGAGGCGG GAGCTCCATGAGCGAAGACGCGTCGGTGGCCGGCATGGAGAGGGCGCAGCTGGAGGAGGAGGCGG T C MIS18A Ensembl:ENSG00000159055 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:32278676..32279050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver Human_RBP_ID_14242687,Human_RBP_ID_17659615,Human_RBP_ID_23923357 116309 RMVar_ID_116309 Human_SNP_ID_843239667 m1A Human chr21 + 45468521 45468521 45468521 GGTCTTGCTGGGCGTGAAGCTCTCTGGGGTGCAGGACGGGCACCAGGACATCTCCCTGCTCTACA GGTCTTGCTGGGCGTGAAGCTCTCTGGGGTGCGGGACGGGCACCAGGACATCTCCCTGCTCTACA A G COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:45468470..45468588 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue adult_T_cell_lymphoma-leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_928278,Human_RBP_ID_9299320,Human_RBP_ID_22767824 RMVar_hsa_circ_1151,RMVar_hsa_circ_55543,RMVar_hsa_circ_347254,RMVar_hsa_circ_7945 116310 RMVar_ID_116310 Human_SNP_ID_843244064 m1A Human chr21 + 33797510 33797510 33797510 GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGGAAAAAGGCAAACAGGAAGCACAAGACAAGCTGG GGAGGAGAGTGTCAAAAAGAAGGATGGCGAGGGAAAAGGCAAACAGGAAGCACAAGACAAGCTGG A G ITSN1 Ensembl:ENSG00000205726 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:33797339..33797550 26863196 MeRIP-seq:(Medium) rs972530973 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,lymph_node diffuse_large_B_cell_lymphoma 11 haematopoietic and lymphoid tissue Human_RBP_ID_928089,Human_RBP_ID_5529561,Human_RBP_ID_9391449 Human_Splice_Rec_2117793,Human_Splice_Rec_2117867,Human_Splice_Rec_2117925,Human_Splice_Rec_2117999,Human_Splice_Rec_2118075,Human_Splice_Rec_2118131,Human_Splice_Rec_2118185,Human_Splice_Rec_2118237,Human_Splice_Rec_2118341,Human_Splice_Rec_2118375,Human_Splice_Rec_2118403 RMVar_hsa_circ_53649,RMVar_hsa_circ_367983,RMVar_hsa_circ_42984,RMVar_hsa_circ_278358,RMVar_hsa_circ_8711,RMVar_hsa_circ_16621,RMVar_hsa_circ_49537,RMVar_hsa_circ_73893,RMVar_hsa_circ_366775,RMVar_hsa_circ_211930,RMVar_hsa_circ_267203,RMVar_hsa_circ_48563,RMVar_hsa_circ_211934,RMVar_hsa_circ_300094,RMVar_hsa_circ_364521,RMVar_hsa_circ_20438,RMVar_hsa_circ_211936 116311 RMVar_ID_116311 Human_SNP_ID_843331190 m1A Human chr21 + 31671707 31671707 31671707 ATGCCCACTAGAGCGTCTATTTCTCTCTTCCAAGTCTCTGTGCCTGTCCCGGTCAGGGCTCCTCC ATGCCCACTAGAGCGTCTATTTCTCTCTTCCACGTCTCTGTGCCTGTCCCGGTCAGGGCTCCTCC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr21:31671544..31672021;chr21:31671528..31672078 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116312 RMVar_ID_116312 Human_SNP_ID_843366158 m1A Human chr21 - 44807030 44807030 44807030 CCTGTTGTGACAACCATGACAGCTGGAGATGGAGGACGAGGACACCATCGACGTGTTCCAGCAGC CCTGTTGTGACAACCATGACAGCTGGAGATGGGGGACGAGGACACCATCGACGTGTTCCAGCAGC T C SUMO3 Ensembl:ENSG00000184900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44806899..44807062 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_lower_lobe adenocarcinoma,LUAD 4 lung Human_RBP_ID_4676638,Human_RBP_ID_14345413,Human_RBP_ID_17397845,Human_RBP_ID_19110897,Human_RBP_ID_22453995 Human_Splice_Rec_2129812,Human_Splice_Rec_2129818,Human_Splice_Rec_2129824,Human_Splice_Rec_2129830 RMVar_hsa_circ_91531,RMVar_hsa_circ_101684,RMVar_hsa_circ_122462,RMVar_hsa_circ_97155,RMVar_hsa_circ_212600,RMVar_hsa_circ_212602,RMVar_hsa_circ_212603,RMVar_hsa_circ_212601 116313 RMVar_ID_116313 Human_SNP_ID_843378714 m1A Human chr21 + 43804003 43804000 43804003 CTCCGCCTGTGGCTGTGATGACCTTGGGCCAGAAGGTCAAACTCCGAAGACTGAAACTCTGCCTG CTCCGCCTGTGGCTGTGATGACCTTGGGCC___AGGTCAAACTCCGAAGACTGAAACTCTGCCTG CAGA C RRP1 Ensembl:ENSG00000160214 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:43803953..43804039 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..33 33 PRAD 1 - Human_RBP_ID_1605555,Human_RBP_ID_1938099,Human_RBP_ID_3663792,Human_RBP_ID_5240382,Human_RBP_ID_5323717,Human_RBP_ID_14330089,Human_RBP_ID_18168249,Human_RBP_ID_26495463 RMVar_hsa_circ_212526,RMVar_hsa_circ_91899 116314 RMVar_ID_116314 Human_SNP_ID_843417440 m1A Human chr21 + 44313984 44313984 44313984 CTGGCTGTTCATCCCCGAGGCTCCACCCGAGGACGGCTGGGAGAACTTCATGTGTGAGAGGCTGG CTGGCTGTTCATCCCCGAGGCTCCACCCGAGGTCGGCTGGGAGAACTTCATGTGTGAGAGGCTGG A T PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44313933..44314062 26863196 MeRIP-seq:(Medium) rs1057037 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5201849,Human_RBP_ID_14339998,Human_RBP_ID_18193871,Human_RBP_ID_18782586,Human_RBP_ID_19007181 Human_Splice_Rec_2128962,Human_Splice_Rec_2128963,Human_Splice_Rec_2129004,Human_Splice_Rec_2129005,Human_Splice_Rec_2129048,Human_Splice_Rec_2129049,Human_Splice_Rec_2129062,Human_Splice_Rec_2129102 GWAS_ID_7619,GWAS_ID_7620,GWAS_ID_7621,GWAS_ID_7622,GWAS_ID_7623,GWAS_ID_7624 RMVar_hsa_circ_52024,RMVar_hsa_circ_82313,RMVar_hsa_circ_86856,RMVar_hsa_circ_212576,RMVar_hsa_circ_212577,RMVar_hsa_circ_320519,RMVar_hsa_circ_74862,RMVar_hsa_circ_93789,RMVar_hsa_circ_212582,RMVar_hsa_circ_212581,RMVar_hsa_circ_32362 116315 RMVar_ID_116315 Human_SNP_ID_843442165 m1A Human chr21 + 46649675 46649675 46649675 TGACATCATCACCGTGTACCAGCAGAAGGTGGAGGATGTGGTGCTGCCCGAGAAGGTGGACGTGC TGACATCATCACCGTGTACCAGCAGAAGGTGGGGGATGTGGTGCTGCCCGAGAAGGTGGACGTGC A G PRMT2 Ensembl:ENSG00000160310 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:46649626..46649827 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_574442,Human_RBP_ID_7055029,Human_RBP_ID_19007553,Human_RBP_ID_26496104 Human_Splice_Rec_2133407,Human_Splice_Rec_2133421,Human_Splice_Rec_2133435,Human_Splice_Rec_2133455,Human_Splice_Rec_2133467,Human_Splice_Rec_2133487,Human_Splice_Rec_2133511,Human_Splice_Rec_2133531,Human_Splice_Rec_2133543,Human_Splice_Rec_2133551,Human_Splice_Rec_2133559,Human_Splice_Rec_2133565 Human_miRNA_ID_2301901,Human_miRNA_ID_2301902,Human_miRNA_ID_2301903,Human_miRNA_ID_2305163,Human_miRNA_ID_2305164,Human_miRNA_ID_2305165,Human_miRNA_ID_2308429,Human_miRNA_ID_2308430,Human_miRNA_ID_2308431 RMVar_hsa_circ_100531,RMVar_hsa_circ_78656,RMVar_hsa_circ_94649,RMVar_hsa_circ_212785,RMVar_hsa_circ_212786,RMVar_hsa_circ_110991,RMVar_hsa_circ_212787,RMVar_hsa_circ_212788,RMVar_hsa_circ_332109,RMVar_hsa_circ_338782,RMVar_hsa_circ_333584,RMVar_hsa_circ_107943,RMVar_hsa_circ_33088,RMVar_hsa_circ_352687,RMVar_hsa_circ_327112,RMVar_hsa_circ_212793 116316 RMVar_ID_116316 Human_SNP_ID_843446550 m1A Human chr21 - 39212159 39212159 39212159 AATTAGGAGTTTATTCCAAGAATATAGGGTGAAGGACGGGTACCTAGTCAAGGATATTTGCTTGG AATTAGGAGTTTATTCCAAGAATATAGGGTGAGGGACGGGTACCTAGTCAAGGATATTTGCTTGG T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:39212112..39212195 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_61354,RMVar_hsa_circ_1681,RMVar_hsa_circ_57413,RMVar_hsa_circ_212202,RMVar_hsa_circ_95532,RMVar_hsa_circ_118948,RMVar_hsa_circ_212203,RMVar_hsa_circ_285761,RMVar_hsa_circ_368190,RMVar_hsa_circ_66903,RMVar_hsa_circ_28646,RMVar_hsa_circ_49529,RMVar_hsa_circ_15558,RMVar_hsa_circ_283307,RMVar_hsa_circ_314503,RMVar_hsa_circ_212206,RMVar_hsa_circ_212207,RMVar_hsa_circ_355761,RMVar_hsa_circ_287942,RMVar_hsa_circ_314029,RMVar_hsa_circ_16685,RMVar_hsa_circ_50555,RMVar_hsa_circ_75352,RMVar_hsa_circ_29494,RMVar_hsa_circ_212209,RMVar_hsa_circ_212210,RMVar_hsa_circ_212211,RMVar_hsa_circ_280555,RMVar_hsa_circ_346631,RMVar_hsa_circ_271335,RMVar_hsa_circ_212212,RMVar_hsa_circ_37322,RMVar_hsa_circ_212213,RMVar_hsa_circ_282517,RMVar_hsa_circ_288293,RMVar_hsa_circ_301937,RMVar_hsa_circ_369507,RMVar_hsa_circ_282755,RMVar_hsa_circ_43414,RMVar_hsa_circ_265554,RMVar_hsa_circ_42896,RMVar_hsa_circ_102191,RMVar_hsa_circ_212217,RMVar_hsa_circ_21888,RMVar_hsa_circ_23759,RMVar_hsa_circ_14397,RMVar_hsa_circ_212218,RMVar_hsa_circ_212220,RMVar_hsa_circ_212215,RMVar_hsa_circ_212216,RMVar_hsa_circ_212214,RMVar_hsa_circ_295650,RMVar_hsa_circ_319791,RMVar_hsa_circ_359584,RMVar_hsa_circ_301372,RMVar_hsa_circ_294675,RMVar_hsa_circ_44929,RMVar_hsa_circ_74485,RMVar_hsa_circ_41374,RMVar_hsa_circ_125454,RMVar_hsa_circ_212222,RMVar_hsa_circ_212224,RMVar_hsa_circ_212226,RMVar_hsa_circ_7590,RMVar_hsa_circ_212225,RMVar_hsa_circ_212223,RMVar_hsa_circ_367815,RMVar_hsa_circ_212227,RMVar_hsa_circ_52117,RMVar_hsa_circ_360864 116317 RMVar_ID_116317 Human_SNP_ID_843461247 m1A Human chr21 - 44457372 44457372 44457372 CGATGGGGTCCTTGGAGGCGGGGGCGCTGGGCAGAGACTTCAGGTACTCCAGGTGCCTCCGGGCA CGATGGGGTCCTTGGAGGCGGGGGCGCTGGGCGGAGACTTCAGGTACTCCAGGTGCCTCCGGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:44457322..44457472 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 116318 RMVar_ID_116318 Human_SNP_ID_843463747 m1A Human chr21 + 44326827 44326827 44326827 CCGCCTACGTGTCAGGGGAGCTGGAGCACGTGACCCGCCGCACCCTGAGCATGGACAAGGGCTTC CCGCCTACGTGTCAGGGGAGCTGGAGCACGTGCCCCGCCGCACCCTGAGCATGGACAAGGGCTTC A C PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr21:44326777..44326877;chr21:44326776..44327326 32194978 MeRIP-seq:(Medium) rs750136662 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 9 head and neck Human_RBP_ID_780135,Human_RBP_ID_18193875,Human_RBP_ID_22453989,Human_RBP_ID_22533745,Human_RBP_ID_23212582,Human_RBP_ID_26821844,Human_RBP_ID_27490634 RMVar_hsa_circ_86240,RMVar_hsa_circ_212590 116319 RMVar_ID_116319 Human_SNP_ID_843467841 m1A Human chr21 - 43095575 43095575 43095575 CATACATGAGTTATATCTAATGACACTTTGTAATGTATAACGAGTCTTAAACCACTGTGGTCTCC CATACATGAGTTATATCTAATGACACTTTGTAGTGTATAACGAGTCTTAAACCACTGTGGTCTCC T C U2AF1 Ensembl:ENSG00000160201 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2839634 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 17 oesophagus,haematopoietic and lymphoid tissue GWAS_ID_7599,GWAS_ID_7600,GWAS_ID_7601,GWAS_ID_7602 RMVar_hsa_circ_9251,RMVar_hsa_circ_104652,RMVar_hsa_circ_212479,RMVar_hsa_circ_305046,RMVar_hsa_circ_372065,RMVar_hsa_circ_212477,RMVar_hsa_circ_344149,RMVar_hsa_circ_77183,RMVar_hsa_circ_212481,RMVar_hsa_circ_29675,RMVar_hsa_circ_212480,RMVar_hsa_circ_103143,RMVar_hsa_circ_212478,RMVar_hsa_circ_212482 116320 RMVar_ID_116320 Human_SNP_ID_843472286 m1A Human chr21 + 34834523 34834523 34834523 GGTGTGGGCTGACCCTCATGGCTGTGCGCCGCAGCTGCTCCAGTTCACTGAGCCGCTCGGAAAAG GGTGTGGGCTGACCCTCATGGCTGTGCGCCGCCGCTGCTCCAGTTCACTGAGCCGCTCGGAAAAG A C RUNX1 RNACentral:URS00003C5339 misc_RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:34834473..34834630 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue 116321 RMVar_ID_116321 Human_SNP_ID_843474943 m1A Human chr21 - 43864599 43864599 43864599 TCAGGGGTCGCCGCGCGGCGGGCTCGGTGGGGACGGCCCTGCGCGCAGCGGCTCCGCGGAAGGAT TCAGGGGTCGCCGCGCGGCGGGCTCGGTGGGGGCGGCCCTGCGCGCAGCGGCTCCGCGGAAGGAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43864555..43864729 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116322 RMVar_ID_116322 Human_SNP_ID_843485755 m1A Human chr21 + 44139575 44139575 44139575 CAGGGGTCGCTGCTGCCTTCTAATTCAGTTCCAACAGTATGGACCCGGGGTAGCGTCCGATCGCA CAGGGGTCGCTGCTGCCTTCTAATTCAGTTCCGACAGTATGGACCCGGGGTAGCGTCCGATCGCA A G GATD3A Ensembl:ENSG00000160221 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4819377 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_7052048,Human_RBP_ID_14338895 RMVar_hsa_circ_78470,RMVar_hsa_circ_212572 116323 RMVar_ID_116323 Human_SNP_ID_843495197 m1A Human chr21 - 43107569 43107569 43107569 GGGGCGGGGAAGAGCGTCGTCGCGTCCGGGTGACGTCTCCCGAGGGCGTCGGCAGGGTCGGCGGC GGGGCGGGGAAGAGCGTCGTCGCGTCCGGGTGTCGTCTCCCGAGGGCGTCGGCAGGGTCGGCGGC T A U2AF1 Ensembl:ENSG00000160201 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:43107487..43107572 26863410 MeRIP-seq:(Medium) rs1224216686 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_104652,RMVar_hsa_circ_212477,RMVar_hsa_circ_77183,RMVar_hsa_circ_212481 116324 RMVar_ID_116324 Human_SNP_ID_843508125 m1A Human chr21 + 42518425 42518425 42518425 AATGACTCATTTATGAAGCATCTTATTCTGCGACCGAGGCTCAGTGGTCAGTGGCGACGTAAATG AATGACTCATTTATGAAGCATCTTATTCTGCGGCCGAGGCTCAGTGGTCAGTGGCGACGTAAATG A G SLC37A1 Ensembl:ENSG00000160190 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr21:42518394..42518494 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_Splice_Rec_2126139,Human_Splice_Rec_2126181,Human_Splice_Rec_2126221 RMVar_hsa_circ_735,RMVar_hsa_circ_267937,RMVar_hsa_circ_354325,RMVar_hsa_circ_378556,RMVar_hsa_circ_32436 116325 RMVar_ID_116325 Human_SNP_ID_843509694 m1A Human chr21 - 44133714 44133714 44133714 CAGATGCCGCAGCGAGCCTCGAGGCCACCAGGACCCTCACAGCCGCCATTGCGGTGAGGACAGCG CAGATGCCGCAGCGAGCCTCGAGGCCACCAGGGCCCTCACAGCCGCCATTGCGGTGAGGACAGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr21:44133676..44133770;chr21:44133687..44133761;chr21:44133687..44133783;chr21:44133690..44133776 26863196 MeRIP-seq:(Medium) rs968714 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,mouth squamous_cell_carcinoma 13 head and neck GWAS_ID_7617,GWAS_ID_7618 116326 RMVar_ID_116326 Human_SNP_ID_843565186 m1A Human chr21 - 25729741 25729741 25729741 AGGTTCTCCTCTGTCATTCGGTCAGCCGTCTCAGTCCATTTGCGGAGGAACATTGGTGTTACAGC AGGTTCTCCTCTGTCATTCGGTCAGCCGTCTCGGTCCATTTGCGGAGGAACATTGGTGTTACAGC T C ATP5PF Ensembl:ENSG00000154723 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:25729691..25741574 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 9 caecum,large intestine Human_RBP_ID_570084,Human_RBP_ID_1602059,Human_RBP_ID_1934182,Human_RBP_ID_3658883,Human_RBP_ID_4666582,Human_RBP_ID_5323676,Human_RBP_ID_8540028,Human_RBP_ID_9332079,Human_RBP_ID_17284488,Human_RBP_ID_18423580,Human_RBP_ID_18778356,Human_RBP_ID_22454188,Human_RBP_ID_23921061,Human_RBP_ID_24534096,Human_RBP_ID_27025644 Human_Splice_Rec_2112418,Human_Splice_Rec_2112428,Human_Splice_Rec_2112434,Human_Splice_Rec_2112440,Human_Splice_Rec_2112446,Human_Splice_Rec_2112452,Human_Splice_Rec_2112458,Human_Splice_Rec_2112464 116327 RMVar_ID_116327 Human_SNP_ID_843588784 m1A Human chr21 + 42879498 42879498 42879498 GCACAACGCCAGTCCCACAGAGCCCGCCATGTACCCGCCCGCCTCACCGCCATACACATGTGCCA GCACAACGCCAGTCCCACAGAGCCCGCCATGTCCCCGCCCGCCTCACCGCCATACACATGTGCCA A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr21:42879378..42879550;chr21:42879149..42879568 26863196 MeRIP-seq:(Medium) rs771132429 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116328 RMVar_ID_116328 Human_SNP_ID_843607189 m1A Human chr21 - 33504477 33504477 33504477 ACCCATCCTTGCTCCCTTCTTTTAAGGGTTCAAATGCCCATGAGCAAGCCCTGGAAACCGGAGTC ACCCATCCTTGCTCCCTTCTTTTAAGGGTTCAGATGCCCATGAGCAAGCCCTGGAAACCGGAGTC T C GART Ensembl:ENSG00000159131 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV COSMIC 33..33 33 lung mixed_adenosquamous_carcinoma 3 lung Human_RBP_ID_571147,Human_RBP_ID_4669365,Human_RBP_ID_9298825 Human_Splice_Rec_2116876,Human_Splice_Rec_2116877,Human_Splice_Rec_2116918,Human_Splice_Rec_2116919,Human_Splice_Rec_2116960,Human_Splice_Rec_2116961,Human_Splice_Rec_2117000,Human_Splice_Rec_2117001 116329 RMVar_ID_116329 Human_SNP_ID_843609687 m1A Human chr21 + 18857987 18857987 18857987 GTTTATGTGTCAGGGTGGTGACTTCACACGCCATAATGGCACTGGTGGCAAGTCCATCTATGGGG GTTTATGTGTCAGGGTGGTGACTTCACACGCCTTAATGGCACTGGTGGCAAGTCCATCTATGGGG A T PPIAP22 Ensembl:ENSG00000198618 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5100712,Human_RBP_ID_9123861,Human_RBP_ID_18201390 116330 RMVar_ID_116330 Human_SNP_ID_843615268 m1A Human chr21 + 33549867 33549867 33549867 TTAGAAACTCTGAAGCCAGCTACAAAAACTGCAGAACTGTCAGTTGTATCTACATCAGTAATCTC TTAGAAACTCTGAAGCCAGCTACAAAAACTGCGGAACTGTCAGTTGTATCTACATCAGTAATCTC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs79746820 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1027646,Human_RBP_ID_1603212,Human_RBP_ID_1935747,Human_RBP_ID_2701555,Human_RBP_ID_7040086,Human_RBP_ID_8541238,Human_RBP_ID_8858692,Human_RBP_ID_26344144,Human_RBP_ID_26821722,Human_RBP_ID_27026651,Human_RBP_ID_27301162,Human_RBP_ID_27489655 GWAS_ID_12597,GWAS_ID_12598,GWAS_ID_12599 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 116331 RMVar_ID_116331 Human_SNP_ID_843617932 m1A Human chr21 - 46206723 46206723 46206723 GAAATCCAGATGGAGGGTTCGCCACCTATGAGACCAAGCGTGGGGGGCACTTGCTGGAGCTGCTG GAAATCCAGATGGAGGGTTCGCCACCTATGAGGCCAAGCGTGGGGGGCACTTGCTGGAGCTGCTG T C LSS Ensembl:ENSG00000160285 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:46205852..46206732 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_3961380,Human_RBP_ID_9391874,Human_RBP_ID_19006893,Human_RBP_ID_23009680 Human_Splice_Rec_2132096,Human_Splice_Rec_2132097,Human_Splice_Rec_2132144,Human_Splice_Rec_2132145,Human_Splice_Rec_2132188,Human_Splice_Rec_2132189,Human_Splice_Rec_2132232,Human_Splice_Rec_2132233 RMVar_hsa_circ_112693,RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_123146,RMVar_hsa_circ_77659,RMVar_hsa_circ_98025,RMVar_hsa_circ_212705,RMVar_hsa_circ_212707,RMVar_hsa_circ_212708,RMVar_hsa_circ_212706,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709,RMVar_hsa_circ_212711,RMVar_hsa_circ_78546,RMVar_hsa_circ_122251,RMVar_hsa_circ_85662,RMVar_hsa_circ_212713,RMVar_hsa_circ_59149,RMVar_hsa_circ_212712 116332 RMVar_ID_116332 Human_SNP_ID_843636163 m1A Human chr21 + 25683938 25683938 25683938 GCCCCAAAAGACCAACAAGTAGTCACAGCAGTAGAGTACCAAGGTACAGTATCTTACTGATTTTC GCCCCAAAAGACCAACAAGTAGTCACAGCAGTGGAGTACCAAGGTACAGTATCTTACTGATTTTC A G JAM2 Ensembl:ENSG00000154721 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8133602 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA,oesophagus squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 16 oesophagus,stomach,large intestine,haematopoietic and lymphoid tissue Human_Splice_Rec_2112338,Human_Splice_Rec_2112339,Human_Splice_Rec_2112356,Human_Splice_Rec_2112357,Human_Splice_Rec_2112374,Human_Splice_Rec_2112375 RMVar_hsa_circ_306192,RMVar_hsa_circ_344362 116333 RMVar_ID_116333 Human_SNP_ID_843659905 m1A Human chr21 - 46227677 46227677 46227677 TTTTTCGATCTCTTTGCAGAAGAATTACTTTAAGGACTTGCCCAAAGCCCACACCGCCTTTGAGG TTTTTCGATCTCTTTGCAGAAGAATTACTTTACGGACTTGCCCAAAGCCCACACCGCCTTTGAGG T G LSS Ensembl:ENSG00000160285 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:46227530..46227716 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_3961407,Human_RBP_ID_4683197,Human_RBP_ID_7053892,Human_RBP_ID_9391556,Human_RBP_ID_14357421 Human_Splice_Rec_2132070,Human_Splice_Rec_2132118,Human_Splice_Rec_2132162,Human_Splice_Rec_2132206,Human_Splice_Rec_2132248,Human_Splice_Rec_2132262,Human_Splice_Rec_2132274 RMVar_hsa_circ_79164,RMVar_hsa_circ_265360,RMVar_hsa_circ_212704,RMVar_hsa_circ_98025,RMVar_hsa_circ_212708,RMVar_hsa_circ_85178,RMVar_hsa_circ_212709 116334 RMVar_ID_116334 Human_SNP_ID_843696686 m1A Human chr21 + 45504520 45504510 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCC__________GGCCCCCCAGGCCCACGTGGCTACCCTGGGAT CCGGCCCCCCA C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1555874527 Functional Loss DEL TCGA 24..33 33 COAD 2 - Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 116335 RMVar_ID_116335 Human_SNP_ID_843728940 m1A Human chr21 + 26051013 26051013 26051013 AACACAAAGGCCACCTTACCTCCCATCTGCATAGTCTGTGTCTGCTCCGCCCCACCAGACATCCG AACACAAAGGCCACCTTACCTCCCATCTGCATGGTCTGTGTCTGCTCCGCCCCACCAGACATCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr21:26051001..26051025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - 116336 RMVar_ID_116336 Human_SNP_ID_843729504 m1A Human chr21 + 44326819 44326819 44326819 CAGTATGGCCGCCTACGTGTCAGGGGAGCTGGAGCACGTGACCCGCCGCACCCTGAGCATGGACA CAGTATGGCCGCCTACGTGTCAGGGGAGCTGGCGCACGTGACCCGCCGCACCCTGAGCATGGACA A C PFKL Ensembl:ENSG00000141959 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr21:44326770..44326965 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_19007232,Human_RBP_ID_22453989,Human_RBP_ID_22533745,Human_RBP_ID_27490634 RMVar_hsa_circ_86240,RMVar_hsa_circ_212590 116337 RMVar_ID_116337 Human_SNP_ID_843734944 m1A Human chr21 - 36257705 36257697 36257706 ACATCTATCTACCTACCTACCTACCTACATCCATCTCTCTACCTACCTACCTACATCTACCTACC ACATCTATCTACCTACCTACCTACCTACATC_________ACCTACCTACCTACATCTACCTACC TAGAGAGATG T CBR3-AS1,CBR3-AS1:2 RNACentral:URS00009B5C87,RNACentral:URS00008BFA9E lincRNA,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:36257676..36257755 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..40 33 SKCA 1 - 116338 RMVar_ID_116338 Human_SNP_ID_843806878 m1A Human chr21 - 33631551 33631551 33631551 TTTCATTTATATATATTTATTTTTAGGTGACTATGAAAGGCTTATATTTCCAACAGAGTTCCACA TTTCATTTATATATATTTATTTTTAGGTGACTGTGAAAGGCTTATATTTCCAACAGAGTTCCACA T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding start codon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33624730..33633693 26863196 MeRIP-seq:(Medium) rs747446935 Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_928085,Human_RBP_ID_3961223,Human_RBP_ID_14262238,Human_RBP_ID_18413029,Human_RBP_ID_25639947 Human_Splice_Rec_2117492,Human_Splice_Rec_2117493,Human_Splice_Rec_2117514,Human_Splice_Rec_2117515,Human_Splice_Rec_2117536,Human_Splice_Rec_2117537,Human_Splice_Rec_2117580,Human_Splice_Rec_2117581,Human_Splice_Rec_2117602,Human_Splice_Rec_2117603,Human_Splice_Rec_2117622,Human_Splice_Rec_2117623,Human_Splice_Rec_2117640,Human_Splice_Rec_2117641,Human_Splice_Rec_2117698,Human_Splice_Rec_2117699,Human_Splice_Rec_2117719,Human_Splice_Rec_2117732,Human_Splice_Rec_2117733,Human_Splice_Rec_2117744,Human_Splice_Rec_2117745,Human_Splice_Rec_2117754 RMVar_hsa_circ_362264,RMVar_hsa_circ_37663,RMVar_hsa_circ_302225,RMVar_hsa_circ_48777,RMVar_hsa_circ_211916,RMVar_hsa_circ_345885,RMVar_hsa_circ_211917,RMVar_hsa_circ_314209 116339 RMVar_ID_116339 Human_SNP_ID_843821262 m1A Human chr21 - 33324799 33324799 33324799 TCTCCAAGCTCCCATTGCCCCATCCTAATTGCAGCACCCCTGTGCGCGCGCGCCTTAGAAATCGC TCTCCAAGCTCCCATTGCCCCATCCTAATTGCGGCACCCCTGTGCGCGCGCGCCTTAGAAATCGC T C lnc-TMEM50B-4,lnc-TMEM50B-4:2,lnc-TMEM50B-4:3,lnc-TMEM50B-4:4 RNACentral:URS0000D596D8,RNACentral:URS00008BFF19,RNACentral:URS0000D5C287,RNACentral:URS0000D57DCC lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr21:33324750..33324825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_5503931 116340 RMVar_ID_116340 Human_SNP_ID_843832001 m1A Human chr21 - 26000182 26000182 26000182 TAAATGTGGTTCCCCACATCTCCTCTGATTAGAGGTGTGCTCTGAACAAGCCGAGACGGGGCCGT TAAATGTGGTTCCCCACATCTCCTCTGATTAGGGGTGTGCTCTGAACAAGCCGAGACGGGGCCGT T C APP Ensembl:ENSG00000142192 Protein coding intron GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr21:26000151..26000200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 10 ovary Human_RBP_ID_1934305,Human_RBP_ID_9391332,Human_RBP_ID_27300572 Human_Splice_Rec_2112578,Human_Splice_Rec_2112612,Human_Splice_Rec_2112674,Human_Splice_Rec_2112704,Human_Splice_Rec_2112742,Human_Splice_Rec_2112770,Human_Splice_Rec_2112796 RMVar_hsa_circ_30326,RMVar_hsa_circ_72605,RMVar_hsa_circ_31488,RMVar_hsa_circ_20814,RMVar_hsa_circ_329745,RMVar_hsa_circ_344082,RMVar_hsa_circ_276290,RMVar_hsa_circ_289014,RMVar_hsa_circ_344865,RMVar_hsa_circ_332936,RMVar_hsa_circ_59446,RMVar_hsa_circ_35844,RMVar_hsa_circ_37023,RMVar_hsa_circ_43543,RMVar_hsa_circ_57301,RMVar_hsa_circ_73432 116341 RMVar_ID_116341 Human_SNP_ID_843841074 m1A Human chr21 - 44324585 44324585 44324585 AGGCGGCGTCGGCCCCCACAGCAATGCCAGTCACGGTGGCCAGGTAGCCACAGTAACCCCCCATG AGGCGGCGTCGGCCCCCACAGCAATGCCAGTCGCGGTGGCCAGGTAGCCACAGTAACCCCCCATG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr21:44324576..44324650;chr21:44324576..44324675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck 116342 RMVar_ID_116342 Human_SNP_ID_843845563 m1A Human chr21 + 32278995 32278995 32278995 CACAGCCGCCAGCGCATCCTCTGCTACACCTCAGTGACCGAACGCCTGCCATTACCTACAAATCG CACAGCCGCCAGCGCATCCTCTGCTACACCTCGGTGACCGAACGCCTGCCATTACCTACAAATCG A G MIS18A-AS1 Ensembl:ENSG00000227256 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr21:32274872..32279050 26863196 MeRIP-seq:(Medium) rs769652796 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116343 RMVar_ID_116343 Human_SNP_ID_843848606 m1A Human chr21 + 25729793 25729793 25729793 CAGAGGAGAACCTGAAGAGCCTCTGAAGAATCATGCTGATTCTGTTACAGAAAACAAGCAGCAGA CAGAGGAGAACCTGAAGAGCCTCTGAAGAATCGTGCTGATTCTGTTACAGAAAACAAGCAGCAGA A G lnc-JAM2-1 RNACentral:URS00008BBFDA lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:25729726..25729825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas adenoma 7 pancreas 116344 RMVar_ID_116344 Human_SNP_ID_843853765 m1A Human chr21 + 33555090 33555090 33555090 GTGGGTAGAAGAAGGAGCTTTAGCATTTCCCCAAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAG GTGGGTAGAAGAAGGAGCTTTAGCATTTCCCCCAGCCGCCGCAGCCGCACCCCCAGCCGCCGCAG A C SON Ensembl:ENSG00000159140 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr21:33554782..33555291;chr21:33554976..33555284;chr21:33554951..33555300 26863196 MeRIP-seq:(Medium) rs202027184 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_1027726,Human_RBP_ID_1603391,Human_RBP_ID_1935832,Human_RBP_ID_8541339,Human_RBP_ID_8858866,Human_RBP_ID_17978952,Human_RBP_ID_18780021,Human_RBP_ID_22262366 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 116345 RMVar_ID_116345 Human_SNP_ID_843862944 m1A Human chr21 - 45531694 45531694 45531694 GCGCCCCAAGCGCAGCCTCTTCTTCAACCGCGACGACCGGGGGCGGTGCGAAACCTCGGCTTCGG GCGCCCCAAGCGCAGCCTCTTCTTCAACCGCGGCGACCGGGGGCGGTGCGAAACCTCGGCTTCGG T C SLC19A1 Ensembl:ENSG00000173638 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:45531533..45531855 26863196 MeRIP-seq:(Medium) rs1327888153 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_208821,Human_RBP_ID_17701430,Human_RBP_ID_18783061,Human_RBP_ID_22767991 Human_miRNA_ID_2917569 RMVar_hsa_circ_212653,RMVar_hsa_circ_114076,RMVar_hsa_circ_122079,RMVar_hsa_circ_212657,RMVar_hsa_circ_294117,RMVar_hsa_circ_212652,RMVar_hsa_circ_292604,RMVar_hsa_circ_212659,RMVar_hsa_circ_376209,RMVar_hsa_circ_212656,RMVar_hsa_circ_338680,RMVar_hsa_circ_212658 116346 RMVar_ID_116346 Human_SNP_ID_843906047 m1A Human chr21 + 45941706 45941706 45941706 ACGTCCGAGGTCACCGGGATGGGCACGCTGTAATCCTACCCAGCACCCTTCCCCCGCGTCACCCA ACGTCCGAGGTCACCGGGATGGGCACGCTGTATTCCTACCCAGCACCCTTCCCCCGCGTCACCCA A T PCBP3 Ensembl:ENSG00000183570 Protein coding stop codon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr21:45940136..45941856 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_Splice_Rec_2131234,Human_Splice_Rec_2131288,Human_Splice_Rec_2131314,Human_Splice_Rec_2131338,Human_Splice_Rec_2131364,Human_Splice_Rec_2131406,Human_Splice_Rec_2131430,Human_Splice_Rec_2131454 116347 RMVar_ID_116347 Human_SNP_ID_843923592 m1A Human chr21 + 31659834 31659834 31659834 CGACGGCCCAGTGCAGGGCATCATCAATTTCGAGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTT CGACGGCCCAGTGCAGGGCATCATCAATTTCGCGCAGAAGGCAAGGGCTGGGACGGAGGCTTGTT A C SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr21:31659676..31659859 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_245053,Human_RBP_ID_928521,Human_RBP_ID_4680203,Human_RBP_ID_5323483,Human_RBP_ID_9332361,Human_RBP_ID_17659679,Human_RBP_ID_22261870 RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 116348 RMVar_ID_116348 Human_SNP_ID_843927661 m1A Human chr21 + 43798026 43798026 43798026 ACTGGACACACAGGATGAGGAGGTGGCGTCGGACAGTGATGAGTCCTCTGAGGGTGGTGAGCGTG ACTGGACACACAGGATGAGGAGGTGGCGTCGGGCAGTGATGAGTCCTCTGAGGGTGGTGAGCGTG A G RRP1 Ensembl:ENSG00000160214 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr21:43797890..43798028 26863196 MeRIP-seq:(Medium) rs371358839 Functional Loss SNV COSMIC 33..33 33 lung non_small_cell_carcinoma 1 lung Human_RBP_ID_4675041,Human_RBP_ID_14329738,Human_RBP_ID_19007158,Human_RBP_ID_27820729 Human_Splice_Rec_2128109,Human_Splice_Rec_2128129,Human_Splice_Rec_2128143 RMVar_hsa_circ_30766,RMVar_hsa_circ_98709,RMVar_hsa_circ_212523,RMVar_hsa_circ_212526,RMVar_hsa_circ_91899,RMVar_hsa_circ_364247,RMVar_hsa_circ_47254,RMVar_hsa_circ_79467,RMVar_hsa_circ_70958,RMVar_hsa_circ_212527 116349 RMVar_ID_116349 Human_SNP_ID_843933043 m1A Human chr21 + 25362417 25362417 25362417 TTGACAAATACACAGAGGTCCTCAAGACCCACAGACTCCTGGTCTGAGCCCAATAAAGACTGTTA TTGACAAATACACAGAGGTCCTCAAGACCCACGGACTCCTGGTCTGAGCCCAATAAAGACTGTTA A G RPL13AP7 Ensembl:ENSG00000213885 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1023836361 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1902685 116350 RMVar_ID_116350 Human_SNP_ID_843935551 m1A Human chr21 - 39177540 39177540 39177540 GTTCTAAGCTACTGTCAAGTATGGAAAATCCCAGCAATTCTGTACTTGTGTTATACTGATGTGAT GTTCTAAGCTACTGTCAAGTATGGAAAATCCCGGCAATTCTGTACTTGTGTTATACTGATGTGAT T C PSMG1 Ensembl:ENSG00000183527 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs14194 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,ESCA,large_intestine adenocarcinoma 5 head and neck,large intestine Human_RBP_ID_928904,Human_RBP_ID_1937081,Human_RBP_ID_18781108,Human_RBP_ID_25650385,Human_RBP_ID_26821789 Human_Splice_Rec_2122214,Human_Splice_Rec_2122218,Human_Splice_Rec_2122230,Human_Splice_Rec_2122240,Human_Splice_Rec_2122250 Human_miRNA_ID_1359235 GWAS_ID_12609,GWAS_ID_12610,GWAS_ID_12611,GWAS_ID_12612 RMVar_hsa_circ_10504,RMVar_hsa_circ_212200,RMVar_hsa_circ_113415,RMVar_hsa_circ_325090,RMVar_hsa_circ_350529 116351 RMVar_ID_116351 Human_SNP_ID_843941336 m1A Human chr21 - 36413121 36413121 36413121 GTTGGGGCTGGGGCCTGTCTGGCCTGAGGGGGAGTCGTGCCGGGGCTGCTGGGGTCTTGGGTTCT GTTGGGGCTGGGGCCTGTCTGGCCTGAGGGGGGGTCGTGCCGGGGCTGCTGGGGTCTTGGGTTCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr21:36413070..36413270 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LIHC 1 - 116352 RMVar_ID_116352 Human_SNP_ID_843971680 m1A Human chr21 - 33617253 33617253 33617253 CTAGCACTTCGGGAGGCCAAAGCGGGTGGATCAGTTGAGGTCAGGAGTTCAAGACCAGCCTGGCC CTAGCACTTCGGGAGGCCAAAGCGGGTGGATCGGTTGAGGTCAGGAGTTCAAGACCAGCCTGGCC T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr21:33617164..33617293 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas RMVar_hsa_circ_362264,RMVar_hsa_circ_15358,RMVar_hsa_circ_35609,RMVar_hsa_circ_37663,RMVar_hsa_circ_72207,RMVar_hsa_circ_302225,RMVar_hsa_circ_48777,RMVar_hsa_circ_211916 116353 RMVar_ID_116353 Human_SNP_ID_843981312 m1A Human chr21 + 45504520 45504520 45504520 GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCAGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT GGCTCCAGCCTGCCCGGCCCCCCCGGCCCCCCCGGCCCCCCAGGCCCACGTGGCTACCCTGGGAT A C COL18A1 Ensembl:ENSG00000182871 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs28696990 Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_3961366,Human_RBP_ID_18168348,Human_RBP_ID_18471380,Human_RBP_ID_19007356,Human_RBP_ID_22454048,Human_RBP_ID_22767976 Human_Splice_Rec_2130847,Human_Splice_Rec_2130927,Human_Splice_Rec_2131007,Human_Splice_Rec_2131051 RMVar_hsa_circ_347254,RMVar_hsa_circ_16826,RMVar_hsa_circ_339250,RMVar_hsa_circ_48241,RMVar_hsa_circ_348055 116354 RMVar_ID_116354 Human_SNP_ID_841145113 m1A Human chr20 + 62325476 62325476 62325476 GTGAGAAGAGGGCACGGATCTGCAGCTGCTCCAGGCTGGCCAGCACCATCATGAGCTCCTCGCGG GTGAGAAGAGGGCACGGATCTGCAGCTGCTCCGGGCTGGCCAGCACCATCATGAGCTCCTCGCGG A G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:62325451..62325475 26863196 MeRIP-seq:(Medium) rs757727996 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 116355 RMVar_ID_116355 Human_SNP_ID_841150328 m1A Human chr20 + 13810996 13810996 13810996 GTCATTATAGGGAATGAGAAGGTGAACTGACCATCAACAGGAGGTGGCAGCTCAGGACCAGGCAC GTCATTATAGGGAATGAGAAGGTGAACTGACCTTCAACAGGAGGTGGCAGCTCAGGACCAGGCAC A T NDUFAF5 Ensembl:ENSG00000101247 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13810945..13811056 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14038399 116356 RMVar_ID_116356 Human_SNP_ID_841155462 m1A Human chr20 - 35742009 35742009 35742009 TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG TTAACAGTAGCAACAGAAGCGGCGGCGGCGGCGGCAGCAGCAGCAGCAGCAGCAATCTCTTCCCG T C RBM39 Ensembl:ENSG00000131051 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:35741891..35742262 26863196 MeRIP-seq:(Medium) rs543109948 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_22257639,Human_RBP_ID_22817373,Human_RBP_ID_25627402,Human_RBP_ID_27020297 Human_Splice_Rec_2077791,Human_Splice_Rec_2077825,Human_Splice_Rec_2077859,Human_Splice_Rec_2077893,Human_Splice_Rec_2077951,Human_Splice_Rec_2077983,Human_Splice_Rec_2078017,Human_Splice_Rec_2078051,Human_Splice_Rec_2078103,Human_Splice_Rec_2078135,Human_Splice_Rec_2078169,Human_Splice_Rec_2078325,Human_Splice_Rec_2078341,Human_Splice_Rec_2078391,Human_Splice_Rec_2078417,Human_Splice_Rec_2078433,Human_Splice_Rec_2078447,Human_Splice_Rec_2078457,Human_Splice_Rec_2078465,Human_Splice_Rec_2078471,Human_Splice_Rec_2078477 RMVar_hsa_circ_47906,RMVar_hsa_circ_353222,RMVar_hsa_circ_61747 116357 RMVar_ID_116357 Human_SNP_ID_841167546 m1A Human chr20 - 57359185 57359185 57359185 TACAAAAAAATAAAAGGAACTCAGCAAATCTTACCCCGCCTGTTTACCAAAAACATCACCTCTAG TACAAAAAAATAAAAGGAACTCAGCAAATCTTCCCCCGCCTGTTTACCAAAAACATCACCTCTAG T G MTRNR2L3 Ensembl:ENSG00000256222 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:57358997..57359214;chr20:57359068..57359225;chr20:57358972..57359222;chr20:57359036..57359236 26863196 MeRIP-seq:(Medium) rs967975492 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116358 RMVar_ID_116358 Human_SNP_ID_841202439 m1A Human chr20 + 63706406 63706406 63706406 GCAGCTCTTCCTGCCCTCCTAAGTCCCAGAACATGAGCCGAGCCTTTCCCACATCCACAGTGCCG GCAGCTCTTCCTGCCCTCCTAAGTCCCAGAACTTGAGCCGAGCCTTTCCCACATCCACAGTGCCG A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63706331..63706438 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 8 kidney 116359 RMVar_ID_116359 Human_SNP_ID_841208607 m1A Human chr20 - 18466914 18466911 18466914 CCGATCCCGGGCCCCGCGGTTAGAGGAAGAGGAGGGCGGCTAGAGGAGGGGAAGAGCTTCCCTTA CCGATCCCGGGCCCCGCGGTTAGAGGAAGAGG___GCGGCTAGAGGAGGGGAAGAGCTTCCCTTA CCCT C DZANK1 Ensembl:ENSG00000089091 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:18466897..18467006 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..35 33 PBCA 1 - Human_Splice_Rec_2064193,Human_Splice_Rec_2064303 116360 RMVar_ID_116360 Human_SNP_ID_841220186 m1A Human chr20 + 34540732 34540732 34540732 ACTAGCACATGGCAGTCGCTTGGAACCCACTCACACCAATCCAGTGACCGTGTGTGGGCTGGCGG ACTAGCACATGGCAGTCGCTTGGAACCCACTCGCACCAATCCAGTGACCGTGTGTGGGCTGGCGG A G ITCH,DYNLRB1 Ensembl:ENSG00000078747,Ensembl:ENSG00000125971 Protein coding,Protein coding 3'UTR,3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:34540681..34540768 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_562193,Human_RBP_ID_5148365,Human_RBP_ID_6993001,Human_RBP_ID_14077933,Human_RBP_ID_17281123,Human_RBP_ID_17395129,Human_RBP_ID_17512850,Human_RBP_ID_17659018,Human_RBP_ID_17970151,Human_RBP_ID_23901184,Human_RBP_ID_27484734,Human_RBP_ID_27564443 Human_miRNA_ID_2767750 RMVar_hsa_circ_112595,RMVar_hsa_circ_209558 116361 RMVar_ID_116361 Human_SNP_ID_841220780 m1A Human chr20 - 62813057 62813057 62813057 TGGGGTGCCCCGATGGGGCAGGGGACCCGGCAAGGGCCAAGGTCTGGGCACCACCACTGGCCACC TGGGGTGCCCCGATGGGGCAGGGGACCCGGCATGGGCCAAGGTCTGGGCACCACCACTGGCCACC T A lnc-TCFL5-6 RNACentral:URS00008C27C3 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:62812960..62813109 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 116362 RMVar_ID_116362 Human_SNP_ID_841222135 m1A Human chr20 - 35284494 35284494 35284494 GCCGGCCTTGAACTCCCGCCTCCGCCGCCCCTAGGCCTCATGGCGGTCCGAGCTTCGTTCGAGAA GCCGGCCTTGAACTCCCGCCTCCGCCGCCCCTGGGCCTCATGGCGGTCCGAGCTTCGTTCGAGAA T C EIF6 Ensembl:ENSG00000242372 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:35284351..35284691 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_779254,Human_RBP_ID_926800,Human_RBP_ID_1303789,Human_RBP_ID_3655843,Human_RBP_ID_3960173,Human_RBP_ID_4643420,Human_RBP_ID_5383647,Human_RBP_ID_8204928,Human_RBP_ID_9430758,Human_RBP_ID_19106320,Human_RBP_ID_21895338,Human_RBP_ID_22549148,Human_RBP_ID_22670829,Human_RBP_ID_27484865 RMVar_hsa_circ_95804,RMVar_hsa_circ_209676,RMVar_hsa_circ_86203,RMVar_hsa_circ_209677,RMVar_hsa_circ_113546,RMVar_hsa_circ_76715,RMVar_hsa_circ_209679,RMVar_hsa_circ_209681 116363 RMVar_ID_116363 Human_SNP_ID_841224522 m1A Human chr20 + 3784572 3784572 3784572 GGGCCTGTTGCAGGACCAGGGGAAGCATTACTAAAGGATCTGGGGCTCTGCACTCTGGCTCCATG GGGCCTGTTGCAGGACCAGGGGAAGCATTACTGAAGGATCTGGGGCTCTGCACTCTGGCTCCATG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:3784551..3784575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 116364 RMVar_ID_116364 Human_SNP_ID_841228310 m1A Human chr20 - 47236339 47236339 47236339 TGCCTCAGCTGATGTCGCCGCTGATATTGCCAAGTACACTAGCAAAGTGAGTGGATGGGAGAGCT TGCCTCAGCTGATGTCGCCGCTGATATTGCCATGTACACTAGCAAAGTGAGTGGATGGGAGAGCT T A ZMYND8 Ensembl:ENSG00000101040 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:47236326..47236500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_8534620,Human_RBP_ID_9390867,Human_RBP_ID_26343059,Human_RBP_ID_27820359 Human_Splice_Rec_2091503,Human_Splice_Rec_2091545,Human_Splice_Rec_2091589,Human_Splice_Rec_2091631,Human_Splice_Rec_2091677,Human_Splice_Rec_2091725,Human_Splice_Rec_2091793,Human_Splice_Rec_2091835,Human_Splice_Rec_2091877,Human_Splice_Rec_2091913,Human_Splice_Rec_2091959,Human_Splice_Rec_2092003,Human_Splice_Rec_2092047,Human_Splice_Rec_2092087,Human_Splice_Rec_2092129,Human_Splice_Rec_2092173 Human_miRNA_ID_2133109 RMVar_hsa_circ_295620,RMVar_hsa_circ_73732,RMVar_hsa_circ_349408,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_210471,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_293394,RMVar_hsa_circ_27798,RMVar_hsa_circ_288021,RMVar_hsa_circ_286280,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,RMVar_hsa_circ_283612,RMVar_hsa_circ_348224,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210474,RMVar_hsa_circ_47077,RMVar_hsa_circ_210475,RMVar_hsa_circ_210473 116365 RMVar_ID_116365 Human_SNP_ID_841233163 m1A Human chr20 - 23637758 23637758 23637758 GCCGGCTCCAGTCCCGGCAAGCCGCCGCGCCTAGTGGGAGGCCCCATGGACGCCAGCGTGGAGGA GCCGGCTCCAGTCCCGGCAAGCCGCCGCGCCTGGTGGGAGGCCCCATGGACGCCAGCGTGGAGGA T C CST3 Ensembl:ENSG00000101439 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs6138024 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,caecum adenocarcinoma,COCA,large_intestine adenocarcinoma 17 caecum,head and neck,large intestine Human_RBP_ID_831459,Human_RBP_ID_927301,Human_RBP_ID_4638381,Human_RBP_ID_17659254,Human_RBP_ID_22452945,Human_RBP_ID_26488961 Human_miRNA_ID_2868883 RMVar_hsa_circ_209078,RMVar_hsa_circ_91022,RMVar_hsa_circ_209079,RMVar_hsa_circ_96177 116366 RMVar_ID_116366 Human_SNP_ID_841236595 m1A Human chr20 + 35542887 35542887 35542887 AACAGCAGCTGGATGTGGAACACAACCTGTTCAAGCAACGACTAGATAAAGATGGCATCCCCGTG AACAGCAGCTGGATGTGGAACACAACCTGTTCGAGCAACGACTAGATAAAGATGGCATCCCCGTG A G ERGIC3 Ensembl:ENSG00000125991 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35542837..35542988 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_1595679,Human_RBP_ID_1928570,Human_RBP_ID_18471106,Human_RBP_ID_19004109 Human_Splice_Rec_2076328,Human_Splice_Rec_2076329,Human_Splice_Rec_2076352,Human_Splice_Rec_2076353,Human_Splice_Rec_2076378,Human_Splice_Rec_2076379,Human_Splice_Rec_2076390,Human_Splice_Rec_2076396,Human_Splice_Rec_2076397,Human_Splice_Rec_2076406,Human_Splice_Rec_2076412,Human_Splice_Rec_2076413,Human_Splice_Rec_2076452,Human_Splice_Rec_2076453,Human_Splice_Rec_2076461,Human_Splice_Rec_2076478,Human_Splice_Rec_2076479,Human_Splice_Rec_2076486,Human_Splice_Rec_2076487 116367 RMVar_ID_116367 Human_SNP_ID_841265999 m1A Human chr20 - 44810516 44810516 44810516 CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA CCAGAGCGCGCTGCGCCGCCACCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCAGCAGCACA T C RIMS4 Ensembl:ENSG00000101098 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HeLa cell line,mRNA;HEK293T cell line,total RNA chr20:44810228..44810560;chr20:44810378..44810606 26863196 MeRIP-seq:(Medium) rs868482057 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116368 RMVar_ID_116368 Human_SNP_ID_841284120 m1A Human chr20 + 44065930 44065930 44065930 CTGCCAGGCCTCAGTGCGTCCCCGCCGCCGCCACCCTCCTTCCCGCTCAGCCCCACACTGCACCA CTGCCAGGCCTCAGTGCGTCCCCGCCGCCGCCGCCCTCCTTCCCGCTCAGCCCCACACTGCACCA A G TOX2 Ensembl:ENSG00000124191 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:44065880..44066110 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma,LGG 6 pancreas RMVar_hsa_circ_103865,RMVar_hsa_circ_210297 116369 RMVar_ID_116369 Human_SNP_ID_841288634 m1A Human chr20 + 43710015 43710015 43710015 AGTACTCCATGGACAACACTCCCCACACGCCAACCCCGTTCAAGAACGCCCTGGAGAAGTACGGA AGTACTCCATGGACAACACTCCCCACACGCCAGCCCCGTTCAAGAACGCCCTGGAGAAGTACGGA A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:43709951..43710050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_8854970,Human_RBP_ID_14115272,Human_RBP_ID_17281567,Human_RBP_ID_17395527,Human_RBP_ID_17511712,Human_RBP_ID_18773690,Human_RBP_ID_22533645,Human_RBP_ID_27486030 Human_Splice_Rec_2086282,Human_Splice_Rec_2086283,Human_Splice_Rec_2086308,Human_Splice_Rec_2086309 Human_miRNA_ID_3096617 RMVar_hsa_circ_96108,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_210276,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_348575,RMVar_hsa_circ_76011,RMVar_hsa_circ_210277,RMVar_hsa_circ_84691,RMVar_hsa_circ_102413,RMVar_hsa_circ_210286,RMVar_hsa_circ_124852,RMVar_hsa_circ_371245,RMVar_hsa_circ_210282,RMVar_hsa_circ_275164,RMVar_hsa_circ_210288,RMVar_hsa_circ_96591,RMVar_hsa_circ_210287,RMVar_hsa_circ_210285,RMVar_hsa_circ_104618,RMVar_hsa_circ_210289,RMVar_hsa_circ_210290 116370 RMVar_ID_116370 Human_SNP_ID_841301633 m1A Human chr20 + 36050701 36050701 36050701 GAGACCCGGGTGCCGGCGGGGTCCGGGCTGGGAGACGCCACGGCCGCCATTAGTCACCGAGGTGG GAGACCCGGGTGCCGGCGGGGTCCGGGCTGGGGGACGCCACGGCCGCCATTAGTCACCGAGGTGG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:36050651..36050725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_209822,RMVar_hsa_circ_209823 116371 RMVar_ID_116371 Human_SNP_ID_841301711 m1A Human chr20 - 63738942 63738942 63738942 GCTGTCAGCTGTGAGGCGGGGCGGGGCGGGGGACGGGCCTCACTCTGGAGGAAGGAGCACAGGTC GCTGTCAGCTGTGAGGCGGGGCGGGGCGGGGGGCGGGCCTCACTCTGGAGGAAGGAGCACAGGTC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:63738805..63739026;chr20:63738899..63739031 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 116372 RMVar_ID_116372 Human_SNP_ID_841306447 m1A Human chr20 + 1393052 1393052 1393052 GGCGGGCGGCGCGACGGGCGGCGTGGACCAACAGCGACCTGGCGGCGGTTCCACGGCTCTGCCTA GGCGGGCGGCGCGACGGGCGGCGTGGACCAACCGCGACCTGGCGGCGGTTCCACGGCTCTGCCTA A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:1392851..1393100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 116373 RMVar_ID_116373 Human_SNP_ID_841310892 m1A Human chr20 + 62306698 62306698 62306698 GCCTGCTGGGAAACATGAGCCACAGCCAGCTCATGCAGCTCATCGGACCAGCCGGCCTTGGAGGA GCCTGCTGGGAAACATGAGCCACAGCCAGCTCGTGCAGCTCATCGGACCAGCCGGCCTTGGAGGA A G ADRM1 Ensembl:ENSG00000130706 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:62306628..62306777;chr20:62306611..62306752;chr20:62306606..62306781;chr20:62306615..62306750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1600162,Human_RBP_ID_22453605 Human_Splice_Rec_2101438,Human_Splice_Rec_2101439,Human_Splice_Rec_2101454,Human_Splice_Rec_2101455,Human_Splice_Rec_2101472,Human_Splice_Rec_2101473,Human_Splice_Rec_2101486,Human_Splice_Rec_2101490 Human_miRNA_ID_2894902,Human_miRNA_ID_2894903 RMVar_hsa_circ_101576,RMVar_hsa_circ_111727,RMVar_hsa_circ_211190,RMVar_hsa_circ_125445,RMVar_hsa_circ_122843,RMVar_hsa_circ_211191,RMVar_hsa_circ_93957,RMVar_hsa_circ_211193,RMVar_hsa_circ_211192,RMVar_hsa_circ_211195 116374 RMVar_ID_116374 Human_SNP_ID_841324418 m1A Human chr20 - 35547488 35547488 35547488 TCCCCGCCAGCTCACTTGATATCTTCTGCCTCAGCACCATAGCAGCTCTCACAGCGATCAGGGTC TCCCCGCCAGCTCACTTGATATCTTCTGCCTCGGCACCATAGCAGCTCTCACAGCGATCAGGGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35547369..35547557 26863196 MeRIP-seq:(Medium) rs768853849 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 10 large intestine 116375 RMVar_ID_116375 Human_SNP_ID_841333594 m1A Human chr20 - 4699574 4699574 4699574 ATGTAGCCGCCAAGGCCCCCCACCACTGCCCCAGCTGCTGCAGCACCAGCCATGTGCTTCATGTT ATGTAGCCGCCAAGGCCCCCCACCACTGCCCCTGCTGCTGCAGCACCAGCCATGTGCTTCATGTT T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:4699526..4699775 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 116376 RMVar_ID_116376 Human_SNP_ID_841337902 m1A Human chr20 + 4699613 4699613 4699613 GTGGTGGGGGGCCTTGGCGGCTACATGCTGGGAAGTGCCATGAGCAGGCCCATCATACATTTCGG GTGGTGGGGGGCCTTGGCGGCTACATGCTGGGGAGTGCCATGAGCAGGCCCATCATACATTTCGG A G PRNP Ensembl:ENSG00000171867 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:4699230..4699624 32194978 MeRIP-seq:(Medium) rs772735889 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_244601,Human_RBP_ID_779238,Human_RBP_ID_9354002,Human_RBP_ID_18471236,Human_RBP_ID_22452885,Human_RBP_ID_22766920 Human_miRNA_ID_421372,Human_miRNA_ID_2134663 RMVar_hsa_circ_94105,RMVar_hsa_circ_99728,RMVar_hsa_circ_208542,RMVar_hsa_circ_85307,RMVar_hsa_circ_208541,RMVar_hsa_circ_208543 116377 RMVar_ID_116377 Human_SNP_ID_841338203 m1A Human chr20 + 35284575 35284575 35284575 ATCCCGGCCTCCGTCCCTCAGGCCCCGCCGCGACCCCGCCCCTCTCGGCCTCCCGGCCCCTCCGT ATCCCGGCCTCCGTCCCTCAGGCCCCGCCGCGCCCCCGCCCCTCTCGGCCTCCCGGCCCCTCCGT A C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:35284551..35284700 26863196 MeRIP-seq:(Medium) rs888943220 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 116378 RMVar_ID_116378 Human_SNP_ID_841355481 m1A Human chr20 + 35556128 35556128 35556128 CCCCTGGACCACACCAATGTCACTGCGCCCCAAGGTACCAGCCCGGGAGGCAGCCCCCAGCCGCA CCCCTGGACCACACCAATGTCACTGCGCCCCATGGTACCAGCCCGGGAGGCAGCCCCCAGCCGCA A T ERGIC3 Ensembl:ENSG00000125991 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35556103..35556189 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_18193639,Human_RBP_ID_19106344,Human_RBP_ID_22767307,Human_RBP_ID_26820801 Human_Splice_Rec_2076338,Human_Splice_Rec_2076339,Human_Splice_Rec_2076364,Human_Splice_Rec_2076365,Human_Splice_Rec_2076424,Human_Splice_Rec_2076425,Human_Splice_Rec_2076442,Human_Splice_Rec_2076443,Human_Splice_Rec_2076470,Human_Splice_Rec_2076471,Human_Splice_Rec_2076496,Human_Splice_Rec_2076497,Human_Splice_Rec_2076510,Human_Splice_Rec_2076511,Human_Splice_Rec_2076514,Human_Splice_Rec_2076515,Human_Splice_Rec_2076521,Human_Splice_Rec_2076529 RMVar_hsa_circ_32149,RMVar_hsa_circ_209703,RMVar_hsa_circ_85841,RMVar_hsa_circ_35436,RMVar_hsa_circ_118312,RMVar_hsa_circ_375570,RMVar_hsa_circ_209704,RMVar_hsa_circ_209705,RMVar_hsa_circ_209707,RMVar_hsa_circ_108117,RMVar_hsa_circ_286271,RMVar_hsa_circ_209706 116379 RMVar_ID_116379 Human_SNP_ID_841361638 m1A Human chr20 + 2657217 2657217 2657217 AGAAAACAGCAGTAGTACTCCAGAGGAGTGTGAGGTCAGTAGGCAGCACGGCCCTGGCAGAGATC AGAAAACAGCAGTAGTACTCCAGAGGAGTGTGGGGTCAGTAGGCAGCACGGCCCTGGCAGAGATC A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2657193..2657344 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_925153,Human_RBP_ID_1197761,Human_RBP_ID_1927254,Human_RBP_ID_5384421,Human_RBP_ID_9388501,Human_RBP_ID_14056145,Human_RBP_ID_19105842,Human_RBP_ID_24546824,Human_RBP_ID_26342316,Human_RBP_ID_27819521 Human_Splice_Rec_2055117,Human_Splice_Rec_2055155,Human_Splice_Rec_2055215,Human_Splice_Rec_2055229,Human_Splice_Rec_2055237,Human_Splice_Rec_2055245,Human_Splice_Rec_2055261,Human_Splice_Rec_2055263 Human_miRNA_ID_2451164 RMVar_hsa_circ_85077,RMVar_hsa_circ_208321,RMVar_hsa_circ_56433,RMVar_hsa_circ_105665,RMVar_hsa_circ_208324 116380 RMVar_ID_116380 Human_SNP_ID_841369275 m1A Human chr20 - 35508182 35508182 35508182 CCACTGGACAAGAAGAGGGGTCACCTGCTCCAAGGTACTCCGCAGCTGGACATTGTGGCGCTGCA CCACTGGACAAGAAGAGGGGTCACCTGCTCCATGGTACTCCGCAGCTGGACATTGTGGCGCTGCA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35503305..35511883 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 3 uterus 116381 RMVar_ID_116381 Human_SNP_ID_841371398 m1A Human chr20 - 41029069 41029069 41029069 CCTGGGAATCGTTGTGGAGGTGGTCCCCACTCATGTCGGCCCGGAGGGACGAGCGCGGCGGCAGG CCTGGGAATCGTTGTGGAGGTGGTCCCCACTCGTGTCGGCCCGGAGGGACGAGCGCGGCGGCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:41028915..41029144 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 116382 RMVar_ID_116382 Human_SNP_ID_841376573 m1A Human chr20 - 48929737 48929737 48929737 GTTTCCCCAACAACTGTTTTCCTCTCTGCCATAGAGCCTTCACTCAGGTTGTTCCCTCTGCTGAA GTTTCCCCAACAACTGTTTTCCTCTCTGCCATTGAGCCTTCACTCAGGTTGTTCCCTCTGCTGAA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:48929735..48929867 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116383 RMVar_ID_116383 Human_SNP_ID_841389171 m1A Human chr20 + 63734762 63734762 63734762 TGGGACCTGCAGCTCTGCCTTTGCTGGCTGGGAGGTGCACACGCGAGGTATAGGCTCCAGACTCC TGGGACCTGCAGCTCTGCCTTTGCTGGCTGGGTGGTGCACACGCGAGGTATAGGCTCCAGACTCC A T AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63708602..63736142 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 5 biliary tract,gallbladder Human_RBP_ID_926334,Human_RBP_ID_3960476,Human_RBP_ID_9391233,Human_RBP_ID_18777203,Human_RBP_ID_23005296,Human_RBP_ID_23119624,Human_RBP_ID_23916423 Human_Splice_Rec_2104868,Human_Splice_Rec_2104869,Human_Splice_Rec_2104880,Human_Splice_Rec_2104881,Human_Splice_Rec_2104891,Human_Splice_Rec_2104902,Human_Splice_Rec_2104903,Human_Splice_Rec_2104916,Human_Splice_Rec_2104917,Human_Splice_Rec_2104929,Human_Splice_Rec_2104944,Human_Splice_Rec_2104949,Human_Splice_Rec_2104956,Human_Splice_Rec_2104957 RMVar_hsa_circ_18652 116384 RMVar_ID_116384 Human_SNP_ID_841389303 m1A Human chr20 - 58830339 58830339 58830339 GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTGATGGTGGTGGTGATGATGATGGTGTGGTGGTGG GTTGTGGTGGTGGTGATGGTGGTGTGGTGGTGGTGGTGGTGGTGATGATGATGGTGTGGTGGTGG T C GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:58830337..58830517 26863196 MeRIP-seq:(Medium) rs897778410 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5652405,Human_RBP_ID_23913425 116385 RMVar_ID_116385 Human_SNP_ID_841389468 m1A Human chr20 - 9403317 9403317 9403317 TCTTTTCTGGCTCCACTTTTAACTAGGGCTCCACTTGGGCCTTCTTTTCCACCTTTCCTTGTGAA TCTTTTCTGGCTCCACTTTTAACTAGGGCTCCGCTTGGGCCTTCTTTTCCACCTTTCCTTGTGAA T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:9403268..9403410 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116386 RMVar_ID_116386 Human_SNP_ID_841395910 m1A Human chr20 + 62811586 62811586 62811586 CACGGGCACGGTGGGCCGAGCACAGAACTACCAGAAGCGCTTCCAGAACCTGAACTGGTGAGGCC CACGGGCACGGTGGGCCGAGCACAGAACTACCTGAAGCGCTTCCAGAACCTGAACTGGTGAGGCC A T OGFR Ensembl:ENSG00000060491 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62811440..62811632 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung Human_RBP_ID_568281,Human_RBP_ID_1600235,Human_RBP_ID_5595372,Human_RBP_ID_27488100 Human_Splice_Rec_2102115,Human_Splice_Rec_2102127,Human_Splice_Rec_2102135 RMVar_hsa_circ_59386,RMVar_hsa_circ_211266,RMVar_hsa_circ_88239 116387 RMVar_ID_116387 Human_SNP_ID_841396392 m1A Human chr20 - 33611207 33611207 33611207 GCTGAGTTGTCGAGCACCACAAGTGGCTGGCAATTGCTGATTTGTGAGTGCAGATGATGTGGAGG GCTGAGTTGTCGAGCACCACAAGTGGCTGGCACTTGCTGATTTGTGAGTGCAGATGATGTGGAGG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33611157..33611239 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116388 RMVar_ID_116388 Human_SNP_ID_841396554 m1A Human chr20 - 58889234 58889234 58889234 CCGCGCCGCAGCCCGGAGCCAGAGAGCAGGGGAGCGCCGCGCCGGCCAGCCACCTGACGCAGCCC CCGCGCCGCAGCCCGGAGCCAGAGAGCAGGGGGGCGCCGCGCCGGCCAGCCACCTGACGCAGCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:58889126..58891125;chr20:58889126..58889580;chr20:58889126..58891061;chr20:58889126..58891025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116389 RMVar_ID_116389 Human_SNP_ID_841400348 m1A Human chr20 - 33676799 33676799 33676799 CCACGAGGCCCTCGACTACCACTTCGGCCTCGAGGAGGGCGAGGGCATCAGAGACCTCTTCGACT CCACGAGGCCCTCGACTACCACTTCGGCCTCGGGGAGGGCGAGGGCATCAGAGACCTCTTCGACT T C E2F1 Ensembl:ENSG00000101412 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33676751..33676800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 4 breast Human_RBP_ID_1025477,Human_RBP_ID_8530879,Human_RBP_ID_8853777,Human_RBP_ID_17281063,Human_RBP_ID_17395087,Human_RBP_ID_17511124,Human_RBP_ID_17969874,Human_RBP_ID_22080607,Human_RBP_ID_23000824,Human_RBP_ID_23900503 116390 RMVar_ID_116390 Human_SNP_ID_841423957 m1A Human chr20 - 63702201 63702201 63702201 TGGTGCTTCCTCCCAGTATTATGCGGAGTGTCACGGCGTCATCTACGTCATTGACTCCACCGACG TGGTGCTTCCTCCCAGTATTATGCGGAGTGTCCCGGCGTCATCTACGTCATTGACTCCACCGACG T G ARFRP1 Ensembl:ENSG00000101246 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:63702103..63702248;chr20:63701793..63702248 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 7 head and neck Human_RBP_ID_1600805,Human_RBP_ID_17976626,Human_RBP_ID_26343265 Human_Splice_Rec_2104744,Human_Splice_Rec_2104745,Human_Splice_Rec_2104758,Human_Splice_Rec_2104759,Human_Splice_Rec_2104772,Human_Splice_Rec_2104773,Human_Splice_Rec_2104782,Human_Splice_Rec_2104783,Human_Splice_Rec_2104802,Human_Splice_Rec_2104803,Human_Splice_Rec_2104816,Human_Splice_Rec_2104817,Human_Splice_Rec_2104828,Human_Splice_Rec_2104829,Human_Splice_Rec_2104833,Human_Splice_Rec_2104844,Human_Splice_Rec_2104845,Human_Splice_Rec_2104854,Human_Splice_Rec_2104855 RMVar_hsa_circ_314627 116391 RMVar_ID_116391 Human_SNP_ID_841426328 m1A Human chr20 + 62335075 62335075 62335075 CTGATCCAGTCCAAAGAAGCCATCCTTGCAGGACGCGCAGGCCTGGCCGCACACGTGGGGCTTGC CTGATCCAGTCCAAAGAAGCCATCCTTGCAGGCCGCGCAGGCCTGGCCGCACACGTGGGGCTTGC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62334994..62335112 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116392 RMVar_ID_116392 Human_SNP_ID_841428519 m1A Human chr20 + 56395626 56395626 56395626 CTACAAGCTGATCATTAGCCAGCTGCTATATGACGGCTACATCAGCATCGCCAATGGCCTCATCA CTACAAGCTGATCATTAGCCAGCTGCTATATGGCGGCTACATCAGCATCGCCAATGGCCTCATCA A G CSTF1 Ensembl:ENSG00000101138 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:56395575..56395776 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_566911,Human_RBP_ID_1026817 Human_Splice_Rec_2096279,Human_Splice_Rec_2096286,Human_Splice_Rec_2096287,Human_Splice_Rec_2096291,Human_Splice_Rec_2096295,Human_Splice_Rec_2096305 RMVar_hsa_circ_38370 116393 RMVar_ID_116393 Human_SNP_ID_841437853 m1A Human chr20 - 648246 648246 648246 GTGGCTAATGGTATTGGTTCAACAACTCCACGAAGGTAGGGGTCACGTCTTGGATCCTTTTGCCT GTGGCTAATGGTATTGGTTCAACAACTCCACGGAGGTAGGGGTCACGTCTTGGATCCTTTTGCCT T C SRXN1,AL121758.1 Ensembl:ENSG00000271303,Ensembl:ENSG00000270299 Protein coding,Protein coding 3'UTR,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6053666 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_RBP_ID_4658866,Human_RBP_ID_17975985,Human_RBP_ID_22081227 GWAS_ID_9311,GWAS_ID_9312,GWAS_ID_9313,GWAS_ID_9314,GWAS_ID_9315 116394 RMVar_ID_116394 Human_SNP_ID_841447699 m1A Human chr20 + 34105401 34105401 34105401 TTTTTTCCTAGTGTCCTCTTCATCAGCTTCCAAATCCTTGTCCTCAGTTGGCTCTGGCTCCACTT TTTTTTCCTAGTGTCCTCTTCATCAGCTTCCACATCCTTGTCCTCAGTTGGCTCTGGCTCCACTT A C RALY Ensembl:ENSG00000125970 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:34105376..34105400 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 116395 RMVar_ID_116395 Human_SNP_ID_841452658 m1A Human chr20 + 62322399 62322399 62322399 GGGTGGCACTCGGAGCCCTCGGCGGCCGGTCCACAAGCACACGGGCGGCAGCCCCCGCAGCCATC GGGTGGCACTCGGAGCCCTCGGCGGCCGGTCCGCAAGCACACGGGCGGCAGCCCCCGCAGCCATC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62322251..62322563 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 116396 RMVar_ID_116396 Human_SNP_ID_841463666 m1A Human chr20 + 63708960 63708960 63708960 TGGGCAGGAGGAGGAAGAGGGAGAGGACGAGGAAGAGCTGAGTGGGACAAAGGTGAGCGCGCCCT TGGGCAGGAGGAGGAAGAGGGAGAGGACGAGGCAGAGCTGAGTGGGACAAAGGTGAGCGCGCCCT A C AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:63708051..63709176;chr20:63708525..63709143 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 MESO 1 - Human_RBP_ID_3961095,Human_RBP_ID_19006507,Human_RBP_ID_22081795,Human_RBP_ID_23005049,Human_RBP_ID_23916207 RMVar_hsa_circ_46204 116397 RMVar_ID_116397 Human_SNP_ID_841466881 m1A Human chr20 - 41493581 41493581 41493581 GCTAGAGGAAGATGTAGATCCTGCAAAAGTTAAAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA GCTAGAGGAAGATGTAGATCCTGCAAAAGTTACAGAATTTGAATCTCTTCAAGTTCTCCCTGAAA T G CHD6 Ensembl:ENSG00000124177 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41491812..41493916 32194978 MeRIP-seq:(Medium) rs374043976 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_1929997,Human_RBP_ID_3960259,Human_RBP_ID_17700512,Human_RBP_ID_23002382 Human_Splice_Rec_2084290,Human_Splice_Rec_2084291,Human_Splice_Rec_2084356,Human_Splice_Rec_2084357,Human_Splice_Rec_2084382,Human_Splice_Rec_2084383 RMVar_hsa_circ_84895,RMVar_hsa_circ_210205,RMVar_hsa_circ_11813,RMVar_hsa_circ_3552,RMVar_hsa_circ_3712,RMVar_hsa_circ_47944,RMVar_hsa_circ_210208,RMVar_hsa_circ_299804,RMVar_hsa_circ_327212,RMVar_hsa_circ_66471,RMVar_hsa_circ_115660,RMVar_hsa_circ_210213,RMVar_hsa_circ_210214,RMVar_hsa_circ_305371,RMVar_hsa_circ_295974,RMVar_hsa_circ_8435,RMVar_hsa_circ_23471,RMVar_hsa_circ_210215,RMVar_hsa_circ_361182,RMVar_hsa_circ_314437,RMVar_hsa_circ_210218,RMVar_hsa_circ_289090,RMVar_hsa_circ_363107 116398 RMVar_ID_116398 Human_SNP_ID_841468163 m1A Human chr20 - 62318476 62318476 62318476 ACGGGAGGCCCAGGAGCTCAACAGCCGCAACCAGGAGCGCCTGGAGGAAGCCCTGGTGAGGACCC ACGGGAGGCCCAGGAGCTCAACAGCCGCAACCGGGAGCGCCTGGAGGAAGCCCTGGTGAGGACCC T C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62318451..62318475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_831852,Human_RBP_ID_19006179 Human_Splice_Rec_2101629 RMVar_hsa_circ_127731,RMVar_hsa_circ_51024,RMVar_hsa_circ_82346,RMVar_hsa_circ_102129,RMVar_hsa_circ_265237,RMVar_hsa_circ_211209,RMVar_hsa_circ_112429,RMVar_hsa_circ_211211,RMVar_hsa_circ_211212,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_26149,RMVar_hsa_circ_265778 116399 RMVar_ID_116399 Human_SNP_ID_841472434 m1A Human chr20 - 21337354 21337354 21337354 GTCACCTTTCCTTCTCTTACACTCTATGTTTAATCCATTTGCCAATCCCACTGGTTCTACCTTCA GTCACCTTTCCTTCTCTTACACTCTATGTTTACTCCATTTGCCAATCCCACTGGTTCTACCTTCA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:21337350..21337499 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116400 RMVar_ID_116400 Human_SNP_ID_841485493 m1A Human chr20 - 62841586 62841586 62841586 TACACGGCTTTTTACTTATTTACCTTTTAAATATGCCCCTTTAGCAATTGGAACAAGTTAAATTG TACACGGCTTTTTACTTATTTACCTTTTAAATTTGCCCCTTTAGCAATTGGAACAAGTTAAATTG T A TCFL5 Ensembl:ENSG00000101190 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs12625609 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_7019051,Human_RBP_ID_17019082,Human_RBP_ID_18324263 GWAS_ID_10084,GWAS_ID_10085,GWAS_ID_10086,GWAS_ID_10087,GWAS_ID_10088 RMVar_hsa_circ_98382,RMVar_hsa_circ_269156,RMVar_hsa_circ_211267 116401 RMVar_ID_116401 Human_SNP_ID_841500936 m1A Human chr20 - 62325525 62325521 62325525 TGGACCCACAGGGGAACTTCCGGCATACGGAGACGCGCAACACTGTGTCCCGCGAGGAGCTCATG TGGACCCACAGGGGAACTTCCGGCATACGGAG____GCAACACTGTGTCCCGCGAGGAGCTCATG CGCGT C LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:62325476..62325525 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..36 33 CESC 1 - Human_RBP_ID_62931,Human_RBP_ID_924174,Human_RBP_ID_9389676,Human_RBP_ID_19004563,Human_RBP_ID_22549469,Human_RBP_ID_22671115 Human_Splice_Rec_2101606,Human_Splice_Rec_2101712 Human_miRNA_ID_1997041,Human_miRNA_ID_2229534,Human_miRNA_ID_2505504 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_110398,RMVar_hsa_circ_269129,RMVar_hsa_circ_211218,RMVar_hsa_circ_265778,RMVar_hsa_circ_344560,RMVar_hsa_circ_114824,RMVar_hsa_circ_211221,RMVar_hsa_circ_31782,RMVar_hsa_circ_211222 116402 RMVar_ID_116402 Human_SNP_ID_841520452 m1A Human chr20 - 1180807 1180807 1180807 CCACCTTATCTGGCTGCTTTAGCTCCAGTGCTACAAGGTCCACCCCCTGCTCCCGCCCACCTGAC CCACCTTATCTGGCTGCTTTAGCTCCAGTGCTGCAAGGTCCACCCCCTGCTCCCGCCCACCTGAC T C TMEM74B Ensembl:ENSG00000125895 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:1180756..1181052 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_27483330 116403 RMVar_ID_116403 Human_SNP_ID_841523054 m1A Human chr20 - 3803477 3803477 3803477 CACAGTGGAAAATGAGGATGACTCTCTTGTCCAGGCTACAGGGCGCGATGGGGCTCTTCAGTAGG CACAGTGGAAAATGAGGATGACTCTCTTGTCCGGGCTACAGGGCGCGATGGGGCTCTTCAGTAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:3803426..3803550 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine 116404 RMVar_ID_116404 Human_SNP_ID_841527692 m1A Human chr20 - 3753867 3753867 3753867 GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCACTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC GCCACCCTGCCCCTCCCTCGTCCTCCTCTCCCGCTTCCTCCTCTCTGTGTGCCTCAGTCTCCTGC T C C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2295340 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_563821,Human_RBP_ID_5119136,Human_RBP_ID_5147847,Human_RBP_ID_5503335,Human_RBP_ID_17658959,Human_RBP_ID_18950198,Human_RBP_ID_22081242,Human_RBP_ID_23184179,Human_RBP_ID_26490332,Human_RBP_ID_27296836,Human_RBP_ID_27485642 Human_miRNA_ID_1340288,Human_miRNA_ID_3078934 GWAS_ID_9324 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 116405 RMVar_ID_116405 Human_SNP_ID_841541628 m1A Human chr20 - 35697799 35697799 35697799 CAAGGAAAATGATCTGTTCTGTTGTGTTCAGGACCCCCGGGTGCTTGATGCCATGCTCCCTTACC CAAGGAAAATGATCTGTTCTGTTGTGTTCAGGGCCCCCGGGTGCTTGATGCCATGCTCCCTTACC T C NFS1 Ensembl:ENSG00000244005 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:35697751..35697800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_14087443,Human_RBP_ID_24380030 Human_Splice_Rec_2077590,Human_Splice_Rec_2077614,Human_Splice_Rec_2077652,Human_Splice_Rec_2077676,Human_Splice_Rec_2077698,Human_Splice_Rec_2077730,Human_Splice_Rec_2077742,Human_Splice_Rec_2077750,Human_Splice_Rec_2077758,Human_Splice_Rec_2077768 RMVar_hsa_circ_15582,RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741 116406 RMVar_ID_116406 Human_SNP_ID_841546354 m1A Human chr20 + 35739228 35739227 35739228 TGCTTACATTTAAGTCATCAAGATACAAAAATAAAAAAATTTTCCATATTAACATGTTAAATTTT TGCTTACATTTAAGTCATCAAGATACAAAAAT_AAAAAATTTTCCATATTAACATGTTAAATTTT TA T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:35739226..35739626 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - 116407 RMVar_ID_116407 Human_SNP_ID_841547254 m1A Human chr20 + 19975426 19975426 19975426 ACCAACAGCAGCCTGGAGGACTACGAGGGGGAAAGTGACCAAGAGACCATGGCGCCCCCCATCAA ACCAACAGCAGCCTGGAGGACTACGAGGGGGACAGTGACCAAGAGACCATGGCGCCCCCCATCAA A C RIN2 Ensembl:ENSG00000132669 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:19975377..19975530 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_111672,RMVar_hsa_circ_127553,RMVar_hsa_circ_208947,RMVar_hsa_circ_75817,RMVar_hsa_circ_208949,RMVar_hsa_circ_67425,RMVar_hsa_circ_6525,RMVar_hsa_circ_113006,RMVar_hsa_circ_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208953,RMVar_hsa_circ_278701,RMVar_hsa_circ_208955,RMVar_hsa_circ_23109,RMVar_hsa_circ_208954,RMVar_hsa_circ_321490,RMVar_hsa_circ_208956 116408 RMVar_ID_116408 Human_SNP_ID_841554829 m1A Human chr20 - 3164651 3164651 3164651 TCGCCGAGGAGCGCCGCGTGTGGCTGGAGGAGAAGGAGAAGGTGATCGAGTACCAGAAGCAGCTG TCGCCGAGGAGCGCCGCGTGTGGCTGGAGGAGCAGGAGAAGGTGATCGAGTACCAGAAGCAGCTG T G LZTS3 Ensembl:ENSG00000088899 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3164509..3164864 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate Human_RBP_ID_21983442 116409 RMVar_ID_116409 Human_SNP_ID_841559706 m1A Human chr20 - 31235211 31235211 31235211 CCATTCCATTCCTTTCAATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCATTCCATTCCTTTCAATTCCATTCCTTTCCTTTCCATTCCATTCCATTCCATTCCATTCCATT T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31235160..31235255 26863196 MeRIP-seq:(Medium) rs199967117 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116410 RMVar_ID_116410 Human_SNP_ID_841559882 m1A Human chr20 - 33490262 33490262 33490262 GGCGGCCGCTCCAGGGACGCCTACCATCGCCGAGCGCCGCCGCCGCGCGCCGCCCGCCTCTACCC GGCGGCCGCTCCAGGGACGCCTACCATCGCCGCGCGCCGCCGCCGCGCGCCGCCCGCCTCTACCC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:33490167..33490327 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116411 RMVar_ID_116411 Human_SNP_ID_841561025 m1A Human chr20 + 18162497 18162497 18162497 GGTTGGGGTCAGAAAGAAGGTCAGAGGCCCTGAACAGATAAAGCAGGAGGTAGAGAGTGAGGAGG GGTTGGGGTCAGAAAGAAGGTCAGAGGCCCTGGACAGATAAAGCAGGAGGTAGAGAGTGAGGAGG A G KAT14 Ensembl:ENSG00000149474 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:18162446..18162611 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - RMVar_hsa_circ_60223,RMVar_hsa_circ_208889,RMVar_hsa_circ_89025,RMVar_hsa_circ_349153,RMVar_hsa_circ_289986,RMVar_hsa_circ_208891,RMVar_hsa_circ_368232 116412 RMVar_ID_116412 Human_SNP_ID_841563147 m1A Human chr20 - 60304947 60304947 60304947 AAGCCCCACTGCACGGTGACCCTGCCCTAAGAAGTTTTCCCTGGCTGGCAATAGAGTGAACTGAA AAGCCCCACTGCACGGTGACCCTGCCCTAAGACGTTTTCCCTGGCTGGCAATAGAGTGAACTGAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:60304899..60305060 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116413 RMVar_ID_116413 Human_SNP_ID_841566241 m1A Human chr20 - 31665960 31665960 31665960 TGGCCGGCGTGGTTCTGCTGGGCTCACTCTTCAGTCGGAAATGACCAGACACTGACCATCCACTC TGGCCGGCGTGGTTCTGCTGGGCTCACTCTTCGGTCGGAAATGACCAGACACTGACCATCCACTC T C BCL2L1 Ensembl:ENSG00000171552 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:31665911..31666000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_27564366 116414 RMVar_ID_116414 Human_SNP_ID_841581617 m1A Human chr20 - 17570177 17570177 17570177 TCTTCGCCGCGGCGGTCGCAGGGACGCGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCAGACCGT TCTTCGCCGCGGCGGTCGCAGGGACGCGGGGGGGGGAGCCGGCGGGCAGCGAGTATGCAGACCGT T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:17570076..17591978 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116415 RMVar_ID_116415 Human_SNP_ID_841589790 m1A Human chr20 + 33411274 33411274 33411274 TCCTATCCAAGCTCCCTCTCCATCCCACACACACTCTGGACTTAACTCAGCATCTTGCTCCAGCC TCCTATCCAAGCTCCCTCTCCATCCCACACACGCTCTGGACTTAACTCAGCATCTTGCTCCAGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:33411232..33411379 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116416 RMVar_ID_116416 Human_SNP_ID_841591254 m1A Human chr20 + 49188274 49188274 49188274 GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGAGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC GAGGAGGCGGGCGCCGCCGGGCCGGGGGGGGGGGGCGGTCAAAGGAAGCGGGAGCCGAGAGAGAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,Wild Type;HEK293T,ALKBH3 KO;HEK293T,untreat control chr20:49188176..49188350;chr20:49188126..49188375;chr20:49188213..49188317 26863410 MeRIP-seq:(Medium) rs899220296 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116417 RMVar_ID_116417 Human_SNP_ID_841594730 m1A Human chr20 - 58994921 58994921 58994921 TGAGGGGTCGTGGGAGCCCAGCGCCTGCCTTGAGGGAAATGAACACTGAAAACAGGATTTGGGAG TGAGGGGTCGTGGGAGCCCAGCGCCTGCCTTGGGGGAAATGAACACTGAAAACAGGATTTGGGAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58994130..58994950 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - 116418 RMVar_ID_116418 Human_SNP_ID_841597760 m1A Human chr20 + 1445681 1445681 1445681 CACACAATGCAAGGTACCTGTGGCTGTGGTTAAATTTCTGCACCAGCCTCCCGCCGTCTGCAAGC CACACAATGCAAGGTACCTGTGGCTGTGGTTACATTTCTGCACCAGCCTCCCGCCGTCTGCAAGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:1443826..1445725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 116419 RMVar_ID_116419 Human_SNP_ID_841604270 m1A Human chr20 - 63520884 63520884 63520884 ACCCGCGCGCGGCGCCCCTCACCTGGGCGGCGACCCCTCGCGGGCCTCGGCGCACGATCACGGGT ACCCGCGCGCGGCGCCCCTCACCTGGGCGGCGCCCCCTCGCGGGCCTCGGCGCACGATCACGGGT T G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Wild Type;HEK293T,Starvation treatment chr20:63520793..63520890;chr20:63520799..63520887 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 116420 RMVar_ID_116420 Human_SNP_ID_841615206 m1A Human chr20 - 44622914 44622914 44622914 TTCTGCTTCTCTACAGGCTGTGGACATACTCAAGACAGAGCGGCTGGGACACGGCTACCACACCC TTCTGCTTCTCTACAGGCTGTGGACATACTCATGACAGAGCGGCTGGGACACGGCTACCACACCC T A ADA Ensembl:ENSG00000196839 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:44621053..44622916 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_Splice_Rec_2086879,Human_Splice_Rec_2086898,Human_Splice_Rec_2086899,Human_Splice_Rec_2086920,Human_Splice_Rec_2086921,Human_Splice_Rec_2086939,Human_Splice_Rec_2086954,Human_Splice_Rec_2086955,Human_Splice_Rec_2086974,Human_Splice_Rec_2086975 RMVar_hsa_circ_91289,RMVar_hsa_circ_112705,RMVar_hsa_circ_118339,RMVar_hsa_circ_107051,RMVar_hsa_circ_92423,RMVar_hsa_circ_210335,RMVar_hsa_circ_82667,RMVar_hsa_circ_76893,RMVar_hsa_circ_210337,RMVar_hsa_circ_210338,RMVar_hsa_circ_210336,RMVar_hsa_circ_17660,RMVar_hsa_circ_210333,RMVar_hsa_circ_210334,RMVar_hsa_circ_315522,RMVar_hsa_circ_210332,RMVar_hsa_circ_210343,RMVar_hsa_circ_210345,RMVar_hsa_circ_81724,RMVar_hsa_circ_85154,RMVar_hsa_circ_123895,RMVar_hsa_circ_210347,RMVar_hsa_circ_80821,RMVar_hsa_circ_210346,RMVar_hsa_circ_210344 116421 RMVar_ID_116421 Human_SNP_ID_841626668 m1A Human chr20 - 43686984 43686983 43686984 CTCGCAGATGATGCGGTCCTCCTCCTCGGTCCAGCAAGACTTCTTCACCTCAGGGTTGAGGTGGT CTCGCAGATGATGCGGTCCTCCTCCTCGGTCC_GCAAGACTTCTTCACCTCAGGGTTGAGGTGGT CT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:43686807..43687110 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 OV 1 - 116422 RMVar_ID_116422 Human_SNP_ID_841627947 m1A Human chr20 - 62135025 62135025 62135025 TGTACAACAGAGGGGAAATATGCTCTTGGTCAACTGACCTTGCAGAAAAGACTGGCTTGTTTCCA TGTACAACAGAGGGGAAATATGCTCTTGGTCACCTGACCTTGCAGAAAAGACTGGCTTGTTTCCA T G lnc-PSMA7-1 RNACentral:URS00008B7B44 lincRNA intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr20:62134930..62135030 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116423 RMVar_ID_116423 Human_SNP_ID_841633226 m1A Human chr20 + 2654515 2654515 2654515 TGGGAGTTGGGGATCCCAAGATTGGTGCCGCAATACAGGAGGAGTTAGGGTACAACTGCCAGACT TGGGAGTTGGGGATCCCAAGATTGGTGCCGCAGTACAGGAGGAGTTAGGGTACAACTGCCAGACT A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:2654392..2654584 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_560668,Human_RBP_ID_3960020,Human_RBP_ID_5594910,Human_RBP_ID_9388472,Human_RBP_ID_14056052,Human_RBP_ID_17968935,Human_RBP_ID_18769979,Human_RBP_ID_19003673,Human_RBP_ID_22256286,Human_RBP_ID_23000312,Human_RBP_ID_26342301,Human_RBP_ID_27018461 Human_Splice_Rec_2055103,Human_Splice_Rec_2055131,Human_Splice_Rec_2055141,Human_Splice_Rec_2055165,Human_Splice_Rec_2055175,Human_Splice_Rec_2055183,Human_Splice_Rec_2055187 Human_miRNA_ID_2477915 RMVar_hsa_circ_86547,RMVar_hsa_circ_118370,RMVar_hsa_circ_208314,RMVar_hsa_circ_95458,RMVar_hsa_circ_12818,RMVar_hsa_circ_208315,RMVar_hsa_circ_208316,RMVar_hsa_circ_39307 116424 RMVar_ID_116424 Human_SNP_ID_841635145 m1A Human chr20 - 35278096 35278096 35278096 TCCCTTCTTTCCGCTCCAACGCACGGAGGGTGAGGTCGGTACGCGGTGGTGGCGTCACGGCGCCA TCCCTTCTTTCCGCTCCAACGCACGGAGGGTGGGGTCGGTACGCGGTGGTGGCGTCACGGCGCCA T C AL121753.1,MMP24OS Ensembl:ENSG00000261582,Ensembl:ENSG00000126005 Protein coding,Protein coding intron,exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:35277997..35278125 26863196 MeRIP-seq:(Medium) rs12481346 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4659767,Human_RBP_ID_5384995,Human_RBP_ID_14082015 Human_Splice_Rec_2075643,Human_Splice_Rec_2075651,Human_Splice_Rec_2075657,Human_Splice_Rec_2075663,Human_Splice_Rec_2075667,Human_Splice_Rec_2075673,Human_Splice_Rec_2075679,Human_Splice_Rec_2075683,Human_Splice_Rec_2075685,Human_Splice_Rec_2075689 116425 RMVar_ID_116425 Human_SNP_ID_841635541 m1A Human chr20 + 36230083 36230083 36230083 TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCCACCCCACACCCTTCACCCTCTGTGTCCTGGTCC TCGGCTCCCTCCTCCCCCTTCCCCCTTCCCCCCCCCCACACCCTTCACCCTCTGTGTCCTGGTCC A C EPB41L1 Ensembl:ENSG00000088367 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:36230032..36230150 26863196 MeRIP-seq:(Medium) rs926201306 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 7 ovary Human_RBP_ID_778566,Human_RBP_ID_17086763,Human_RBP_ID_17572167,Human_RBP_ID_17659337,Human_RBP_ID_18950530 Human_miRNA_ID_1704520,Human_miRNA_ID_2946417 RMVar_hsa_circ_98747,RMVar_hsa_circ_209828,RMVar_hsa_circ_124883,RMVar_hsa_circ_209834 116426 RMVar_ID_116426 Human_SNP_ID_841638401 m1A Human chr20 + 50128164 50128164 50128164 GAAGATGATCAGGCAGAAGACGAAGCACTCCCAGGGGTATAGCTGCTCCAGGGCTTCTGCAGGTT GAAGATGATCAGGCAGAAGACGAAGCACTCCCGGGGGTATAGCTGCTCCAGGGCTTCTGCAGGTT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:50127936..50128229 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116427 RMVar_ID_116427 Human_SNP_ID_841643967 m1A Human chr20 + 18504832 18504832 18504832 AGCCGGTTCCACAGCGCGGCACCTGTACCTCCAGGGTGGCGCTGGGGTTGGCTCCATGACCAAGA AGCCGGTTCCACAGCGCGGCACCTGTACCTCCGGGGTGGCGCTGGGGTTGGCTCCATGACCAAGA A G RPS19P1 Ensembl:ENSG00000214612 Pseudogene exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs878914350 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_559832 116428 RMVar_ID_116428 Human_SNP_ID_841647983 m1A Human chr20 + 39018291 39018291 39018291 GCCTGTCCGGTCCTGGAGGTGGTAGAAAGTCCAGACAGTGAGGGGGCAATGGAGATGGCAGAGAA GCCTGTCCGGTCCTGGAGGTGGTAGAAAGTCCGGACAGTGAGGGGGCAATGGAGATGGCAGAGAA A G DHX35 Ensembl:ENSG00000101452 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:39018283..39018482 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_101465,RMVar_hsa_circ_95656,RMVar_hsa_circ_49605,RMVar_hsa_circ_210141,RMVar_hsa_circ_52876,RMVar_hsa_circ_210151,RMVar_hsa_circ_123449,RMVar_hsa_circ_22361,RMVar_hsa_circ_372466,RMVar_hsa_circ_210154,RMVar_hsa_circ_15734,RMVar_hsa_circ_210155 116429 RMVar_ID_116429 Human_SNP_ID_841652171 m1A Human chr20 - 5106269 5106269 5106269 ACCCCTCCTAAGATCCCTTATAAGGCCATCGCACTTGCCACTGTGCTGTTTTTGATTGGCGCCTT ACCCCTCCTAAGATCCCTTATAAGGCCATCGCGCTTGCCACTGTGCTGTTTTTGATTGGCGCCTT T C TMEM230 Ensembl:ENSG00000089063 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6107576 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 8 head and neck Human_RBP_ID_778597,Human_RBP_ID_4653126 Human_Splice_Rec_2057866,Human_Splice_Rec_2057867,Human_Splice_Rec_2057874,Human_Splice_Rec_2057875,Human_Splice_Rec_2057882,Human_Splice_Rec_2057883,Human_Splice_Rec_2057888,Human_Splice_Rec_2057889,Human_Splice_Rec_2057894,Human_Splice_Rec_2057895,Human_Splice_Rec_2057902,Human_Splice_Rec_2057903,Human_Splice_Rec_2057908,Human_Splice_Rec_2057909,Human_Splice_Rec_2057912,Human_Splice_Rec_2057913,Human_Splice_Rec_2057918,Human_Splice_Rec_2057919,Human_Splice_Rec_2057926,Human_Splice_Rec_2057927,Human_Splice_Rec_2057934 Human_miRNA_ID_1996976,Human_miRNA_ID_2229469,Human_miRNA_ID_2505440 RMVar_hsa_circ_270115,RMVar_hsa_circ_345358,RMVar_hsa_circ_208574 116430 RMVar_ID_116430 Human_SNP_ID_841664738 m1A Human chr20 + 59192073 59192073 59192073 GCACCGACTCGGGGTACCTGTCGCGCTCCGACAGCGCGGAGCAGCCGCATGCGCCCTGCAGCCCC GCACCGACTCGGGGTACCTGTCGCGCTCCGACTGCGCGGAGCAGCCGCATGCGCCCTGCAGCCCC A T ZNF831 Ensembl:ENSG00000124203 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:59192024..59192199 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung RMVar_hsa_circ_64755 116431 RMVar_ID_116431 Human_SNP_ID_841667436 m1A Human chr20 - 62879639 62879639 62879639 CAAAGAGAAGCCGCTGGAGGAGCCCGACGCCCAGGGCCGGGCGTCCGAGGACAGGAGGAGAGAGC CAAAGAGAAGCCGCTGGAGGAGCCCGACGCCCGGGGCCGGGCGTCCGAGGACAGGAGGAGAGAGC T C DIDO1 Ensembl:ENSG00000101191 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:62879546..62879671 26863196 MeRIP-seq:(Medium) rs773333280 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116432 RMVar_ID_116432 Human_SNP_ID_841684638 m1A Human chr20 - 62941545 62941545 62941545 CTGGACATGCAAGTTATTGAGCTTTTCCATCCACTCATCTTTCGTGATTTCATCGGGTTTTTCTG CTGGACATGCAAGTTATTGAGCTTTTCCATCCCCTCATCTTTCGTGATTTCATCGGGTTTTTCTG T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:62941476..62941600 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach 116433 RMVar_ID_116433 Human_SNP_ID_841689048 m1A Human chr20 - 45898489 45898489 45898489 AGAAGAGGACTCTCCTAGCGGGAGAGGCTGGGAGGGGCTGCATCAGGCCGTGGAGCTGGTTGCTG AGAAGAGGACTCTCCTAGCGGGAGAGGCTGGGGGGGGCTGCATCAGGCCGTGGAGCTGGTTGCTG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:45898440..45898556 26863196 MeRIP-seq:(Medium) rs754747052 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116434 RMVar_ID_116434 Human_SNP_ID_841700503 m1A Human chr20 - 17967439 17967439 17967439 TGTTCATCTAGTAAGTAAATACCAGAGTTTCAAAGCGGCTGGATTGTTCCAACAAGGGTATCATT TGTTCATCTAGTAAGTAAATACCAGAGTTTCAGAGCGGCTGGATTGTTCCAACAAGGGTATCATT T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2295457 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14043418 116435 RMVar_ID_116435 Human_SNP_ID_841706782 m1A Human chr20 + 62804860 62804860 62804860 CGCCTCCAGCGCGAGCCCCGCCGCCGCCGAGCATGGACGACCCCGACTGCGACTCCACCTGGGAG CGCCTCCAGCGCGAGCCCCGCCGCCGCCGAGCGTGGACGACCCCGACTGCGACTCCACCTGGGAG A G OGFR Ensembl:ENSG00000060491 Protein coding start codon GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr20:62804812..62804914 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_1304941,Human_RBP_ID_4656265,Human_RBP_ID_9391130,Human_RBP_ID_23004800,Human_RBP_ID_27488096 116436 RMVar_ID_116436 Human_SNP_ID_841708378 m1A Human chr20 + 34997318 34997318 34997318 AGAGCGGGCAGCCCGGGCCCGCGTGGAGAAGCAGCGTGCAGAGGCGGCGCGGGAGCTGGAGGAGC AGAGCGGGCAGCCCGGGCCCGCGTGGAGAAGCGGCGTGCAGAGGCGGCGCGGGAGCTGGAGGAGC A G MYH7B Ensembl:ENSG00000078814 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:34997276..34997425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_Splice_Rec_2075372,Human_Splice_Rec_2075454 116437 RMVar_ID_116437 Human_SNP_ID_841708393 m1A Human chr20 - 33680333 33680333 33680333 AGTGGGCCAGCTCGGGGCAGAGGCCGCCATCCAGGAAAAGGTACCTATGGAGCTTGGGCTGGGCA AGTGGGCCAGCTCGGGGCAGAGGCCGCCATCCGGGAAAAGGTACCTATGGAGCTTGGGCTGGGCA T C E2F1 Ensembl:ENSG00000101412 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33680326..33680425 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_924438,Human_RBP_ID_19005395,Human_RBP_ID_19106231 Human_Splice_Rec_2073458,Human_Splice_Rec_2073459 RMVar_hsa_circ_294292,RMVar_hsa_circ_378487,RMVar_hsa_circ_77695,RMVar_hsa_circ_209434,RMVar_hsa_circ_87130,RMVar_hsa_circ_209435,RMVar_hsa_circ_285805,RMVar_hsa_circ_209438 116438 RMVar_ID_116438 Human_SNP_ID_841710060 m1A Human chr20 + 2655416 2655416 2655416 ACTGCCGTCTTGCCCAGTTTATTGGAAACCGAAGGGAACTGAATGAGGACAAGCTGGAGAAGCTG ACTGCCGTCTTGCCCAGTTTATTGGAAACCGAGGGGAACTGAATGAGGACAAGCTGGAGAAGCTG A G NOP56 Ensembl:ENSG00000101361 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:2655366..2655448 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_62482,Human_RBP_ID_1594179,Human_RBP_ID_1927226,Human_RBP_ID_3645255,Human_RBP_ID_4639297,Human_RBP_ID_5597044,Human_RBP_ID_8260291,Human_RBP_ID_8529779,Human_RBP_ID_9388477,Human_RBP_ID_14056076,Human_RBP_ID_18769993,Human_RBP_ID_19004930,Human_RBP_ID_22816988,Human_RBP_ID_23000329,Human_RBP_ID_23898244,Human_RBP_ID_26342306,Human_RBP_ID_27294967,Human_RBP_ID_27819515 Human_Splice_Rec_2055106,Human_Splice_Rec_2055107,Human_Splice_Rec_2055134,Human_Splice_Rec_2055144,Human_Splice_Rec_2055145,Human_Splice_Rec_2055168,Human_Splice_Rec_2055186,Human_Splice_Rec_2055190,Human_Splice_Rec_2055192,Human_Splice_Rec_2055193,Human_Splice_Rec_2055199,Human_Splice_Rec_2055205 Human_miRNA_ID_2255721,Human_miRNA_ID_2959481 RMVar_hsa_circ_86547,RMVar_hsa_circ_118370,RMVar_hsa_circ_208314,RMVar_hsa_circ_95458,RMVar_hsa_circ_76502,RMVar_hsa_circ_12818,RMVar_hsa_circ_208315,RMVar_hsa_circ_208316,RMVar_hsa_circ_127153,RMVar_hsa_circ_208317,RMVar_hsa_circ_208318 116439 RMVar_ID_116439 Human_SNP_ID_841725433 m1A Human chr20 - 3674991 3674991 3674991 AGATGCTTCCATGGGCTCTGGGATGCACCGCCAGAGGTACCCCCCCACCATTCCTACCCCTACTC AGATGCTTCCATGGGCTCTGGGATGCACCGCCGGAGGTACCCCCCCACCATTCCTACCCCTACTC T C ADAM33 Ensembl:ENSG00000149451 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3674857..3675051 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116440 RMVar_ID_116440 Human_SNP_ID_841759663 m1A Human chr20 - 62197901 62197901 62197901 CAGTTTTTACTCCCTCCATCTTCTCCACTGAAACCCTGGTACCGCGACAGGACCGACGACAGGGA CAGTTTTTACTCCCTCCATCTTCTCCACTGAAGCCCTGGTACCGCGACAGGACCGACGACAGGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62197848..62197965 26863196 MeRIP-seq:(Medium) rs1485833504 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 116441 RMVar_ID_116441 Human_SNP_ID_841782450 m1A Human chr20 + 62122652 62122652 62122652 CCCGGCGCTCCTTCCCCACCGCGGCCCGACGCACCCCGGCCGCCGCCATGAGCGGCTCCTCAGGC CCCGGCGCTCCTTCCCCACCGCGGCCCGACGCCCCCCGGCCGCCGCCATGAGCGGCTCCTCAGGC A C LSM14B Ensembl:ENSG00000149657 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HTR8/Svneo,Hypoxia IP chr20:62122451..62122939;chr20:62122609..62122725 26863196,32194978 MeRIP-seq:(Medium) rs767775489 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4655417,Human_RBP_ID_18423191 RMVar_hsa_circ_120149,RMVar_hsa_circ_211148 116442 RMVar_ID_116442 Human_SNP_ID_841796951 m1A Human chr20 - 2836255 2836255 2836255 TGAATCATCCATTCCAGGGAAGCCATAGGCAGACCCCAGACTTCGGGGAGCACCTGGCCTTGCTC TGAATCATCCATTCCAGGGAAGCCATAGGCAGGCCCCAGACTTCGGGGAGCACCTGGCCTTGCTC T C PCED1A Ensembl:ENSG00000132635 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:2836165..2836254 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_560797,Human_RBP_ID_18951139 Human_Splice_Rec_2055602,Human_Splice_Rec_2055614 Human_miRNA_ID_2455915 RMVar_hsa_circ_123458,RMVar_hsa_circ_208347 116443 RMVar_ID_116443 Human_SNP_ID_841799997 m1A Human chr20 - 35346043 35346043 35346043 TGCATTTACAATCCTCTAGCTAGACACAGAGCACTGATTGGTGCAAGTATCCACCCGACCCAGAA TGCATTTACAATCCTCTAGCTAGACACAGAGCGCTGATTGGTGCAAGTATCCACCCGACCCAGAA T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6142349 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14082907,Human_RBP_ID_23901894 RMVar_hsa_circ_316254,RMVar_hsa_circ_344263,RMVar_hsa_circ_323431 116444 RMVar_ID_116444 Human_SNP_ID_841804601 m1A Human chr20 - 23421377 23421377 23421377 GGGCGACATGGACAACGCGGGGAAGGAGCGTGAGGCAGTACAGCTGATGGCGGAGGCCGAGAAGC GGGCGACATGGACAACGCGGGGAAGGAGCGTGCGGCAGTACAGCTGATGGCGGAGGCCGAGAAGC T G NAPB Ensembl:ENSG00000125814 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:23421327..23421464 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_18423280,Human_RBP_ID_19005203 Human_Splice_Rec_2066837,Human_Splice_Rec_2066853,Human_Splice_Rec_2066869,Human_Splice_Rec_2066887,Human_Splice_Rec_2066905,Human_Splice_Rec_2066915,Human_Splice_Rec_2066929 116445 RMVar_ID_116445 Human_SNP_ID_841811293 m1A Human chr20 + 32358685 32358685 32358685 CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCACCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC CTCGCGCGCCGCCGCTGCCACGCGCCCCCCCCCCCGCCGCCGCCGCCCCAGCCCCGCGCCACCGC A C ASXL1 Ensembl:ENSG00000171456 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated chr20:32358417..32358778;chr20:32358599..32358774 26863196 MeRIP-seq:(Medium) rs1020071543 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4641116,Human_RBP_ID_5384845,Human_RBP_ID_9331799,Human_RBP_ID_22533639 Human_miRNA_ID_2387528,Human_miRNA_ID_2389001,Human_miRNA_ID_2400150,Human_miRNA_ID_2686409,Human_miRNA_ID_3031213 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 116446 RMVar_ID_116446 Human_SNP_ID_841819976 m1A Human chr20 + 3800861 3800860 3800861 TGGAGCTGCCAGCAGCTCTGGGGAAGACAAGGAGAATGTGCGCTTCTGGAAGGCCGGGGTGGGAG TGGAGCTGCCAGCAGCTCTGGGGAAGACAAGG_GAATGTGCGCTTCTGGAAGGCCGGGGTGGGAG GA G CDC25B Ensembl:ENSG00000101224 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3800720..3800884 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 OV 1 - Human_Splice_Rec_2057149,Human_Splice_Rec_2057177,Human_Splice_Rec_2057207,Human_Splice_Rec_2057237,Human_Splice_Rec_2057267 RMVar_hsa_circ_44790,RMVar_hsa_circ_94429,RMVar_hsa_circ_208498 116447 RMVar_ID_116447 Human_SNP_ID_841856684 m1A Human chr20 + 33686218 33686218 33686218 GCCGCAGCGCGCCGGCCCCGAGCAGGGCCTCCAGCGCCGGCGCGCATGGGCCGCCCGCAGGGGCC GCCGCAGCGCGCCGGCCCCGAGCAGGGCCTCCGGCGCCGGCGCGCATGGGCCGCCCGCAGGGGCC A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:33686179..33686301 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung 116448 RMVar_ID_116448 Human_SNP_ID_841867008 m1A Human chr20 - 62755298 62755298 62755298 AGGGAGGAAGGAAGGGAGGGAGAGGTAGAGGAATGAATGGAGGGAAGGAGGGAGAGAGGGATGGA AGGGAGGAAGGAAGGGAGGGAGAGGTAGAGGAGTGAATGGAGGGAAGGAGGGAGAGAGGGATGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62755250..62755351 26863196 MeRIP-seq:(Medium) rs867329508 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate 116449 RMVar_ID_116449 Human_SNP_ID_841884456 m1A Human chr20 - 58993096 58993096 58993096 CTCTCCGCCCTCTTACCTCATCCAGCAACGCCAGGTGGACAGGGGTATGGTCAGTCTGCAGCTGA CTCTCCGCCCTCTTACCTCATCCAGCAACGCCCGGTGGACAGGGGTATGGTCAGTCTGCAGCTGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58991875..58993153 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung 116450 RMVar_ID_116450 Human_SNP_ID_841887459 m1A Human chr20 - 2660831 2660831 2660831 CAGGAGCAGAGCTGATGGCCCTGCCCACCCTCAGGCGTAAGTTGGACTTATTTGCCAACGTAGTC CAGGAGCAGAGCTGATGGCCCTGCCCACCCTCGGGCGTAAGTTGGACTTATTTGCCAACGTAGTC T C IDH3B Ensembl:ENSG00000101365 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2660676..2660850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,DLBC 6 haematopoietic and lymphoid tissue Human_RBP_ID_18770071,Human_RBP_ID_22548880 RMVar_hsa_circ_88903,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_208326,RMVar_hsa_circ_208328,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_208335,RMVar_hsa_circ_208339,RMVar_hsa_circ_79896 116451 RMVar_ID_116451 Human_SNP_ID_841900169 m1A Human chr20 - 56484191 56484191 56484191 GAGAAGGAACAAATGGTACATGTCAGGAACTCACCGTGTGGCAAACTTCCGCTTTTATCTCTTTC GAGAAGGAACAAATGGTACATGTCAGGAACTCGCCGTGTGGCAAACTTCCGCTTTTATCTCTTTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:56484169..56484243;chr20:56484176..56484200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 116452 RMVar_ID_116452 Human_SNP_ID_841907372 m1A Human chr20 + 41421178 41421178 41421178 CTAAGACTGCACATATCTACAAACCCACTTTCATTTCCTGGATTCAAGGAAGGGGAAGCTAAACA CTAAGACTGCACATATCTACAAACCCACTTTCGTTTCCTGGATTCAAGGAAGGGGAAGCTAAACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41421132..41421283 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck 116453 RMVar_ID_116453 Human_SNP_ID_841916941 m1A Human chr20 + 63742407 63742407 63742407 CTTCTACTACACAGAGCTGGATGTTGGTGTGGACACGCTGACCGACGGGCTGTCCAGCCTGACTC CTTCTACTACACAGAGCTGGATGTTGGTGTGGGCACGCTGACCGACGGGCTGTCCAGCCTGACTC A G SLC2A4RG Ensembl:ENSG00000125520 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:63742401..63742425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_568799,Human_RBP_ID_1600833,Human_RBP_ID_5472128,Human_RBP_ID_8857140,Human_RBP_ID_18777238,Human_RBP_ID_19006527,Human_RBP_ID_26821131 Human_Splice_Rec_2105066,Human_Splice_Rec_2105082,Human_Splice_Rec_2105086,Human_Splice_Rec_2105094,Human_Splice_Rec_2105098 116454 RMVar_ID_116454 Human_SNP_ID_841918927 m1A Human chr20 + 63284918 63284918 63284918 CCTGAACGAGAACGTCCTCAAGCCTGCGCAGGAGAAGGTAACGGGCAGCTCCGGGTGGTTGTGCC CCTGAACGAGAACGTCCTCAAGCCTGCGCAGGTGAAGGTAACGGGCAGCTCCGGGTGGTTGTGCC A T ARFGAP1 Ensembl:ENSG00000101199 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63284588..63284940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_19006407,Human_RBP_ID_23115492,Human_RBP_ID_27840598 Human_Splice_Rec_2102794,Human_Splice_Rec_2102795,Human_Splice_Rec_2102816,Human_Splice_Rec_2102817,Human_Splice_Rec_2102848,Human_Splice_Rec_2102849,Human_Splice_Rec_2102876,Human_Splice_Rec_2102877,Human_Splice_Rec_2102908,Human_Splice_Rec_2102909,Human_Splice_Rec_2102930,Human_Splice_Rec_2102931,Human_Splice_Rec_2102980,Human_Splice_Rec_2102981,Human_Splice_Rec_2103006,Human_Splice_Rec_2103007,Human_Splice_Rec_2103030,Human_Splice_Rec_2103031,Human_Splice_Rec_2103054,Human_Splice_Rec_2103055,Human_Splice_Rec_2103065,Human_Splice_Rec_2103072,Human_Splice_Rec_2103073,Human_Splice_Rec_2103080,Human_Splice_Rec_2103081,Human_Splice_Rec_2103083 RMVar_hsa_circ_12971,RMVar_hsa_circ_54411 116455 RMVar_ID_116455 Human_SNP_ID_841920748 m1A Human chr20 + 37184270 37184270 37184270 GCCCACTCACTACCTCACCAAGCATGACGTGGAGAGACTAAAAGCCTCGCTGGATCGCCCTTTCA GCCCACTCACTACCTCACCAAGCATGACGTGGGGAGACTAAAAGCCTCGCTGGATCGCCCTTTCA A G RPN2 Ensembl:ENSG00000118705 Protein coding 5'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:37184176..37184375 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas adenoma 2 pancreas Human_RBP_ID_1929274,Human_RBP_ID_3647909,Human_RBP_ID_4659825,Human_RBP_ID_8532520,Human_RBP_ID_14094682,Human_RBP_ID_17396584,Human_RBP_ID_17511456,Human_RBP_ID_18772378 Human_Splice_Rec_2080776,Human_Splice_Rec_2080786,Human_Splice_Rec_2080818,Human_Splice_Rec_2080834,Human_Splice_Rec_2080844 Human_miRNA_ID_2899358,Human_miRNA_ID_2899359 RMVar_hsa_circ_90832,RMVar_hsa_circ_114205,RMVar_hsa_circ_209971,RMVar_hsa_circ_123355,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,RMVar_hsa_circ_328390,RMVar_hsa_circ_347488,RMVar_hsa_circ_209970,RMVar_hsa_circ_344552,RMVar_hsa_circ_277636,RMVar_hsa_circ_123005,RMVar_hsa_circ_100764,RMVar_hsa_circ_102647,RMVar_hsa_circ_93349,RMVar_hsa_circ_209975,RMVar_hsa_circ_209979,RMVar_hsa_circ_45372,RMVar_hsa_circ_84350,RMVar_hsa_circ_209981,RMVar_hsa_circ_209982,RMVar_hsa_circ_209983,RMVar_hsa_circ_209980,RMVar_hsa_circ_209977,RMVar_hsa_circ_209978,RMVar_hsa_circ_209976,RMVar_hsa_circ_209973,RMVar_hsa_circ_209974 116456 RMVar_ID_116456 Human_SNP_ID_841933190 m1A Human chr20 - 25476871 25476871 25476871 CCAGATGTGCGTATCGTTGGCCCTCGAGGAGGAGGAGTTGGAGCTTGCCCGCGGGAAGCGAGTGG CCAGATGTGCGTATCGTTGGCCCTCGAGGAGGGGGAGTTGGAGCTTGCCCGCGGGAAGCGAGTGG T C NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25476833..25477014 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_5119307,Human_RBP_ID_5528959,Human_RBP_ID_18167646,Human_RBP_ID_26342382 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_73820,RMVar_hsa_circ_296399,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209165,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_326296 116457 RMVar_ID_116457 Human_SNP_ID_841934123 m1A Human chr20 + 63495808 63495808 63495808 CAGTGACCCCAGGGGCCCCCAGTGTCCCTTGAAGGGTGCAGCGGCCTCTCCCCCAGCCCCGCCTG CAGTGACCCCAGGGGCCCCCAGTGTCCCTTGAGGGGTGCAGCGGCCTCTCCCCCAGCCCCGCCTG A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:63495806..63495940 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116458 RMVar_ID_116458 Human_SNP_ID_841952550 m1A Human chr20 + 47651121 47651113 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAGCAG_________CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAGCAGCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs749960421 Functional Loss DEL ICGC 26..34 33 STAD 1 - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 116459 RMVar_ID_116459 Human_SNP_ID_841956059 m1A Human chr20 - 50153622 50153622 50153622 CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGAACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG CGATCGGGCGAGTGGCCATGGCGGGCGCCGAGGACTGGCCGGGCCAGCAGCTGGAGCTGGACGAG T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr20:50153526..50153684 26863196 MeRIP-seq:(Medium) rs232733 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 11 head and neck Human_RBP_ID_779577,Human_RBP_ID_4659469,Human_RBP_ID_9331567,Human_RBP_ID_18422924,Human_RBP_ID_22453144,Human_RBP_ID_26491557 116460 RMVar_ID_116460 Human_SNP_ID_841958753 m1A Human chr20 - 36306281 36306281 36306281 CTCCCCGAGAGCGGCGGGGAGGGGGCGGGGAGAGGGGAGAGGAGCGCGGGGGAGGGGGCCGTGCG CTCCCCGAGAGCGGCGGGGAGGGGGCGGGGAGGGGGGAGAGGAGCGCGGGGGAGGGGGCCGTGCG T C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:36306269..36306354 26863410 MeRIP-seq:(Medium) rs1345153966 Functional Loss SNV ICGC 33..33 33 BOCA 1 - 116461 RMVar_ID_116461 Human_SNP_ID_841964732 m1A Human chr20 - 13776062 13776044 13776062 AGTGAAGATGATGAAGAGGAGGATGAAGATGAAGAGGAGGATGAAGATGAGGATAGTGAGGATGA AGTGAAGATGATGAAGAGGAGGATGAAGATGA__________________GGATAGTGAGGATGA CTCATCTTCATCCTCCTCT C ESF1 Ensembl:ENSG00000089048 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13775975..13776225 26863196 MeRIP-seq:(Medium) rs751194986 Functional Loss DEL ICGC 33..50 33 ESCA 1 - Human_RBP_ID_62160,Human_RBP_ID_206546,Human_RBP_ID_1601113,Human_RBP_ID_2677318,Human_RBP_ID_5148298,Human_RBP_ID_6979952,Human_RBP_ID_8260218,Human_RBP_ID_18534380,Human_RBP_ID_21983996,Human_RBP_ID_22081554,Human_RBP_ID_23004742,Human_RBP_ID_23115397,Human_RBP_ID_23119586,Human_RBP_ID_23894563,Human_RBP_ID_24546638,Human_RBP_ID_26342696 RMVar_hsa_circ_361273,RMVar_hsa_circ_358209,RMVar_hsa_circ_75021,RMVar_hsa_circ_319772,RMVar_hsa_circ_61776 116462 RMVar_ID_116462 Human_SNP_ID_841965771 m1A Human chr20 - 62311730 62311730 62311730 CAGCTCCAGCAGATGAAGCCCCACCGGGGACCACCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC CAGCTCCAGCAGATGAAGCCCCACCGGGGACCCCCCCCCGAGCTCCAGCCGCAGCCTGAGGGGCC T G LAMA5 Ensembl:ENSG00000130702 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62311680..62311774 26863196 MeRIP-seq:(Medium) rs1014927606 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_779031,Human_RBP_ID_18167736 Human_Splice_Rec_2101510,Human_Splice_Rec_2101664,Human_Splice_Rec_2101690 RMVar_hsa_circ_97788,RMVar_hsa_circ_91818,RMVar_hsa_circ_51024,RMVar_hsa_circ_93993,RMVar_hsa_circ_211202,RMVar_hsa_circ_211203,RMVar_hsa_circ_97362,RMVar_hsa_circ_211204,RMVar_hsa_circ_211205 116463 RMVar_ID_116463 Human_SNP_ID_841965858 m1A Human chr20 + 62193528 62193528 62193528 TGGGCTGGCCTGAAGCCCAGCCGGCTACTGCCACAGCGGGCTTCTCCCAGGCTGCTCTCGGTCGG TGGGCTGGCCTGAAGCCCAGCCGGCTACTGCCGCAGCGGGCTTCTCCCAGGCTGCTCTCGGTCGG A G MTG2 Ensembl:ENSG00000101181 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:62193478..62193544 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_4659970,Human_RBP_ID_8537701 Human_Splice_Rec_2100863,Human_Splice_Rec_2100867,Human_Splice_Rec_2100875,Human_Splice_Rec_2100887,Human_Splice_Rec_2100893,Human_Splice_Rec_2100899 RMVar_hsa_circ_63687,RMVar_hsa_circ_72877,RMVar_hsa_circ_55819 116464 RMVar_ID_116464 Human_SNP_ID_841968367 m1A Human chr20 - 63521559 63521559 63521559 ACCTGGGGGGTGGGGAATGGCTTCCCCGGGGCACTCGGTACTGCTGCAGGAGCTGTTGCTGGAAG ACCTGGGGGGTGGGGAATGGCTTCCCCGGGGCCCTCGGTACTGCTGCAGGAGCTGTTGCTGGAAG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr20:63521487..63521644;chr20:63521501..63521575;chr20:63521451..63521610 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 116465 RMVar_ID_116465 Human_SNP_ID_841974398 m1A Human chr20 - 34105451 34105451 34105451 TGAGGAAGGGGATACCCAAACAGAGGAAACCCAGCCTTCAGAAACAAAAGAAGTGGAGCCAGAGC TGAGGAAGGGGATACCCAAACAGAGGAAACCCGGCCTTCAGAAACAAAAGAAGTGGAGCCAGAGC T C EIF2S2 Ensembl:ENSG00000125977 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:34103487..34105450 32194978 MeRIP-seq:(Medium) rs1483428965 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_244858,Human_RBP_ID_1595295,Human_RBP_ID_2681784,Human_RBP_ID_8234963,Human_RBP_ID_9389018,Human_RBP_ID_22817172,Human_RBP_ID_24546649,Human_RBP_ID_26342826,Human_RBP_ID_26489635,Human_RBP_ID_27019642,Human_RBP_ID_27819653 Human_Splice_Rec_2073738,Human_Splice_Rec_2073739 RMVar_hsa_circ_4267,RMVar_hsa_circ_19288,RMVar_hsa_circ_59414,RMVar_hsa_circ_363726,RMVar_hsa_circ_369076 116466 RMVar_ID_116466 Human_SNP_ID_841975091 m1A Human chr20 - 59254220 59254220 59254220 CTCGTGATTCAGCACTGTGAATTTCCTGGGCTATGTGATCTGTTCTCACTGGCAGAGAAATACAA CTCGTGATTCAGCACTGTGAATTTCCTGGGCTGTGTGATCTGTTCTCACTGGCAGAGAAATACAA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:59254169..59254265 26863196 MeRIP-seq:(Medium) rs1479242786 Functional Loss SNV TCGA 33..33 33 LUAD 1 - 116467 RMVar_ID_116467 Human_SNP_ID_841990553 m1A Human chr20 + 44006641 44006641 44006641 CCTCCCGGAGCCATCCCTCCTGCACCTGGGGGACCACGAAGCCAGCTACCACTCGCTGTGCCACG CCTCCCGGAGCCATCCCTCCTGCACCTGGGGGGCCACGAAGCCAGCTACCACTCGCTGTGCCACG A G TOX2 Ensembl:ENSG00000124191 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr20:44006502..44006725 26863196 MeRIP-seq:(Medium) rs1174645856 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_Splice_Rec_2086324,Human_Splice_Rec_2086340,Human_Splice_Rec_2086358,Human_Splice_Rec_2086374 RMVar_hsa_circ_8876,RMVar_hsa_circ_37750,RMVar_hsa_circ_103865,RMVar_hsa_circ_210294,RMVar_hsa_circ_285899,RMVar_hsa_circ_96996,RMVar_hsa_circ_210296,RMVar_hsa_circ_210297,RMVar_hsa_circ_210295,RMVar_hsa_circ_308886 116468 RMVar_ID_116468 Human_SNP_ID_841995539 m1A Human chr20 - 56381573 56381573 56381573 AACCAAGTGTTAGAATGTTTATCCTTTGTTGCAGGCATCCTAATATTCTTAGACTGTATGGTTAT AACCAAGTGTTAGAATGTTTATCCTTTGTTGCGGGCATCCTAATATTCTTAGACTGTATGGTTAT T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:56381551..56381575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 8 large intestine RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_211025,RMVar_hsa_circ_4614,RMVar_hsa_circ_270962,RMVar_hsa_circ_294140,RMVar_hsa_circ_335191,RMVar_hsa_circ_281125,RMVar_hsa_circ_211026,RMVar_hsa_circ_211024 116469 RMVar_ID_116469 Human_SNP_ID_842011771 m1A Human chr20 - 408740 408740 408741 GGTCTTCTCGTCCATCTGGCGTGGCTGTGCCCATCCCCCTGGGGGGGACCGTGCCTCCTGGGAAA GGTCTTCTCGTCCATCTGGCGTGGCTGTGCCACTCCCCCTGGGGGGGACCGTGCCTCCTGGGAAA TG GT - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:408690..408792 26863196 MeRIP-seq:(Medium) - Functional Loss MNV ICGC 32..33 33 COCA 1 - 116470 RMVar_ID_116470 Human_SNP_ID_842018253 m1A Human chr20 + 17619727 17619727 17619727 GCTCTGCCTCCAAATGCGACGTGTGCTCCCTCACCTGGACAGATGCACAGACACGCACACGCATG GCTCTGCCTCCAAATGCGACGTGTGCTCCCTCGCCTGGACAGATGCACAGACACGCACACGCATG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:17619701..17619775;chr20:17619676..17621908 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 116471 RMVar_ID_116471 Human_SNP_ID_842031716 m1A Human chr20 + 58903720 58903720 58903720 TGAGCAACCTGGTGCCCCCCGTGGAGCTGGCCAACCCCGAGAACCAGTTCAGAGTGGACTACATC TGAGCAACCTGGTGCCCCCCGTGGAGCTGGCCCACCCCGAGAACCAGTTCAGAGTGGACTACATC A C GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:58903488..58903825 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast basal_(triple-negative)_carcinoma 9 breast Human_RBP_ID_62048,Human_RBP_ID_244157,Human_RBP_ID_567462,Human_RBP_ID_778537,Human_RBP_ID_831171,Human_RBP_ID_1380664,Human_RBP_ID_1932158,Human_RBP_ID_8537179,Human_RBP_ID_9118606,Human_RBP_ID_18193797,Human_RBP_ID_18776045,Human_RBP_ID_23913580,Human_RBP_ID_26821031 Human_Splice_Rec_2098140,Human_Splice_Rec_2098141,Human_Splice_Rec_2098168,Human_Splice_Rec_2098169,Human_Splice_Rec_2098194,Human_Splice_Rec_2098195,Human_Splice_Rec_2098218,Human_Splice_Rec_2098219,Human_Splice_Rec_2098242,Human_Splice_Rec_2098243,Human_Splice_Rec_2098256,Human_Splice_Rec_2098257,Human_Splice_Rec_2098266,Human_Splice_Rec_2098272,Human_Splice_Rec_2098273,Human_Splice_Rec_2098284,Human_Splice_Rec_2098285,Human_Splice_Rec_2098304,Human_Splice_Rec_2098305,Human_Splice_Rec_2098314,Human_Splice_Rec_2098315,Human_Splice_Rec_2098328,Human_Splice_Rec_2098329,Human_Splice_Rec_2098350,Human_Splice_Rec_2098351,Human_Splice_Rec_2098376,Human_Splice_Rec_2098377,Human_Splice_Rec_2098408,Human_Splice_Rec_2098409,Human_Splice_Rec_2098418,Human_Splice_Rec_2098419,Human_Splice_Rec_2098436,Human_Splice_Rec_2098437,Human_Splice_Rec_2098456,Human_Splice_Rec_2098457,Human_Splice_Rec_2098470,Human_Splice_Rec_2098471,Human_Splice_Rec_2098486,Human_Splice_Rec_2098487,Human_Splice_Rec_2098502,Human_Splice_Rec_2098503,Human_Splice_Rec_2098522,Human_Splice_Rec_2098523,Human_Splice_Rec_2098530,Human_Splice_Rec_2098531,Human_Splice_Rec_2098548,Human_Splice_Rec_2098549,Human_Splice_Rec_2098560,Human_Splice_Rec_2098561,Human_Splice_Rec_2098568,Human_Splice_Rec_2098569,Human_Splice_Rec_2098578,Human_Splice_Rec_2098579,Human_Splice_Rec_2098590,Human_Splice_Rec_2098591,Human_Splice_Rec_2098614,Human_Splice_Rec_2098615,Human_Splice_Rec_2098636,Human_Splice_Rec_2098637,Human_Splice_Rec_2098660,Human_Splice_Rec_2098661,Human_Splice_Rec_2098682,Human_Splice_Rec_2098683,Human_Splice_Rec_2098704,Human_Splice_Rec_2098705,Human_Splice_Rec_2098744,Human_Splice_Rec_2098745,Human_Splice_Rec_2098762,Human_Splice_Rec_2098763,Human_Splice_Rec_2098776,Human_Splice_Rec_2098777,Human_Splice_Rec_2098794,Human_Splice_Rec_2098795,Human_Splice_Rec_2098804,Human_Splice_Rec_2098805,Human_Splice_Rec_2098824,Human_Splice_Rec_2098825,Human_Splice_Rec_2098842,Human_Splice_Rec_2098843,Human_Splice_Rec_2098860,Human_Splice_Rec_2098861,Human_Splice_Rec_2098870,Human_Splice_Rec_2098871,Human_Splice_Rec_2098879 Human_miRNA_ID_1348167,Human_miRNA_ID_1811355,Human_miRNA_ID_2921413 RMVar_hsa_circ_3455,RMVar_hsa_circ_14526,RMVar_hsa_circ_278184,RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_70998,RMVar_hsa_circ_344347,RMVar_hsa_circ_211085,RMVar_hsa_circ_211086,RMVar_hsa_circ_374022,RMVar_hsa_circ_211088,RMVar_hsa_circ_211087,RMVar_hsa_circ_374296,RMVar_hsa_circ_10317 116472 RMVar_ID_116472 Human_SNP_ID_842043781 m1A Human chr20 - 17620764 17620762 17620765 CAGAGACCTGCAGAAGAGCGTGGAGGAGGAGGAGCAGGTGTGGAGGGCCAAGGTGGGCGCCGCAG CAGAGACCTGCAGAAGAGCGTGGAGGAGGAG___CAGGTGTGGAGGGCCAAGGTGGGCGCCGCAG GCTC G RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17620656..17620851 26863196 MeRIP-seq:(Medium) rs765361650 Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_925314,Human_RBP_ID_8857471,Human_RBP_ID_9388702,Human_RBP_ID_17976683,Human_RBP_ID_18471050,Human_RBP_ID_19005127,Human_RBP_ID_22452908,Human_RBP_ID_26343398 Human_Splice_Rec_2063282,Human_Splice_Rec_2063283,Human_Splice_Rec_2063322,Human_Splice_Rec_2063323,Human_Splice_Rec_2063364,Human_Splice_Rec_2063365,Human_Splice_Rec_2063412,Human_Splice_Rec_2063413,Human_Splice_Rec_2063458,Human_Splice_Rec_2063459,Human_Splice_Rec_2063504,Human_Splice_Rec_2063505,Human_Splice_Rec_2063548,Human_Splice_Rec_2063549 RMVar_hsa_circ_59520,RMVar_hsa_circ_62648 116473 RMVar_ID_116473 Human_SNP_ID_842055800 m1A Human chr20 - 17570173 17570173 17570173 CGCCGCGGCGGTCGCAGGGACGCGGGGGAGGGAGCCGGCGGGCAGCGAGTATGCAGACCGTCCTC CGCCGCGGCGGTCGCAGGGACGCGGGGGAGGGGGCCGGCGGGCAGCGAGTATGCAGACCGTCCTC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:17570076..17570273 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116474 RMVar_ID_116474 Human_SNP_ID_842068549 m1A Human chr20 - 62337889 62337889 62337889 CGGGGAGCCCTGGACCAGCTCTGTGGGGCGGGAGGTTTGTGCCGCTGCCGCCCCGGCTACACAGG CGGGGAGCCCTGGACCAGCTCTGTGGGGCGGGTGGTTTGTGCCGCTGCCGCCCCGGCTACACAGG T A LAMA5 Ensembl:ENSG00000130702 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:62337876..62337900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_5383134,Human_RBP_ID_9298704,Human_RBP_ID_18412953 Human_Splice_Rec_2101554,Human_Splice_Rec_2101555 Human_miRNA_ID_2389028 RMVar_hsa_circ_127731,RMVar_hsa_circ_265237,RMVar_hsa_circ_211215,RMVar_hsa_circ_78215,RMVar_hsa_circ_211223,RMVar_hsa_circ_44783,RMVar_hsa_circ_104880,RMVar_hsa_circ_211232,RMVar_hsa_circ_211233,RMVar_hsa_circ_312216 116475 RMVar_ID_116475 Human_SNP_ID_842071344 m1A Human chr20 + 62165544 62165544 62165544 GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGAGCGTAAGCGCCACACGCAGCAGAGTTAAGACG GGGGTAAGGAGCACGGCTGCGTGCTGGGCTCGCGCGTAAGCGCCACACGCAGCAGAGTTAAGACG A C SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62165534..62165605 26863196 MeRIP-seq:(Medium) rs201669693 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,COCA,large_intestine adenocarcinoma 8 lung,large intestine Human_RBP_ID_19006129,Human_RBP_ID_19106926 RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 116476 RMVar_ID_116476 Human_SNP_ID_842087478 m1A Human chr20 + 298704 298704 298704 GAGCCCTTACTGCCGGAAGGGCATCGTGTGCAACCTCTGTGGCAAGCGAGGACACGCCTTTGCCC GAGCCCTTACTGCCGGAAGGGCATCGTGTGCAGCCTCTGTGGCAAGCGAGGACACGCCTTTGCCC A G ZCCHC3 Ensembl:ENSG00000247315 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:298545..298800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_1025172,Human_RBP_ID_6987061,Human_RBP_ID_8853192,Human_RBP_ID_9297813,Human_RBP_ID_9353989,Human_RBP_ID_14056258 116477 RMVar_ID_116477 Human_SNP_ID_842094646 m1A Human chr20 - 63627003 63627003 63627003 GCCGCCGCCGCCCGCCGCCGCCGCAGCTCCCGACGCCGCCGCCCCCGCCGGGTGCCTAAGCAGGC GCCGCCGCCGCCCGCCGCCGCCGCAGCTCCCGCCGCCGCCGCCCCCGCCGGGTGCCTAAGCAGGC T G GMEB2 Ensembl:ENSG00000101216 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr20:63626901..63627064 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_2104135 116478 RMVar_ID_116478 Human_SNP_ID_842105467 m1A Human chr20 + 35954252 35954252 35954252 AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCAGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT AGTTTCTCCGGTGGCACCGCCGCGGGACTCCCTGTGGCCGCCAAGATCGGCTCCGTAGCCGCCAT A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:35953626..35954565;chr20:35953965..35954500 26863196 MeRIP-seq:(Medium) rs955575094 Functional Loss SNV TCGA 33..33 33 OV 1 - 116479 RMVar_ID_116479 Human_SNP_ID_842119525 m1A Human chr20 - 59006381 59006381 59006381 TGGTGTCAACTATGCCAGCATCACCCGGAACCAGCACATCCCCCAATACTGCGGCTCCTGCTGGG TGGTGTCAACTATGCCAGCATCACCCGGAACCGGCACATCCCCCAATACTGCGGCTCCTGCTGGG T C CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr20:59006285..59006516;chr20:59006301..59007075 26863196,32194978 MeRIP-seq:(Medium) rs748470022 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue Human_RBP_ID_18209356,Human_RBP_ID_22767066,Human_RBP_ID_27487665 Human_Splice_Rec_2099117,Human_Splice_Rec_2099127,Human_Splice_Rec_2099133 Human_miRNA_ID_272941,Human_miRNA_ID_1322162,Human_miRNA_ID_2653749,Human_miRNA_ID_2754947 RMVar_hsa_circ_57119,RMVar_hsa_circ_302597,RMVar_hsa_circ_211101,RMVar_hsa_circ_81573,RMVar_hsa_circ_211102,RMVar_hsa_circ_372909,RMVar_hsa_circ_211103 116480 RMVar_ID_116480 Human_SNP_ID_842125007 m1A Human chr20 - 33394043 33394043 33394043 TCCATTCAGGCAGATGTGATTCTCCTTGTCACATGCTCTATCAGGTGCGAATTTGTTCTTTTCCT TCCATTCAGGCAGATGTGATTCTCCTTGTCACGTGCTCTATCAGGTGCGAATTTGTTCTTTTCCT T C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs291700 Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 13 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_5384896,Human_RBP_ID_9347994,Human_RBP_ID_19005357,Human_RBP_ID_19107971,Human_RBP_ID_25626906 Human_Splice_Rec_2072774,Human_Splice_Rec_2072775,Human_Splice_Rec_2072802,Human_Splice_Rec_2072803,Human_Splice_Rec_2072828,Human_Splice_Rec_2072829,Human_Splice_Rec_2072854,Human_Splice_Rec_2072855,Human_Splice_Rec_2072882,Human_Splice_Rec_2072883,Human_Splice_Rec_2072948,Human_Splice_Rec_2072949,Human_Splice_Rec_2072960,Human_Splice_Rec_2072961 GWAS_ID_14801,GWAS_ID_14802,GWAS_ID_14803,GWAS_ID_14804,GWAS_ID_14805,GWAS_ID_14806,GWAS_ID_14807,GWAS_ID_14808,GWAS_ID_14809,GWAS_ID_14810,GWAS_ID_14811,GWAS_ID_14812,GWAS_ID_14813,GWAS_ID_14814,GWAS_ID_14815,GWAS_ID_14816,GWAS_ID_14817,GWAS_ID_14818,GWAS_ID_14819,GWAS_ID_14820,GWAS_ID_14821,GWAS_ID_14822,GWAS_ID_14823,GWAS_ID_14824,GWAS_ID_14825,GWAS_ID_14826,GWAS_ID_14827,GWAS_ID_14828,GWAS_ID_14829,GWAS_ID_14830,GWAS_ID_14831,GWAS_ID_14832,GWAS_ID_14833,GWAS_ID_14834,GWAS_ID_14835,GWAS_ID_14836,GWAS_ID_14837,GWAS_ID_14838,GWAS_ID_14839,GWAS_ID_14840,GWAS_ID_14841,GWAS_ID_14842,GWAS_ID_14843,GWAS_ID_14844,GWAS_ID_14845,GWAS_ID_14846,GWAS_ID_14847,GWAS_ID_14848,GWAS_ID_14849,GWAS_ID_14850,GWAS_ID_14851 RMVar_hsa_circ_31033,RMVar_hsa_circ_78082,RMVar_hsa_circ_209378,RMVar_hsa_circ_301190,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_25879,RMVar_hsa_circ_375733,RMVar_hsa_circ_301731,RMVar_hsa_circ_54544,RMVar_hsa_circ_209393,RMVar_hsa_circ_209394,RMVar_hsa_circ_209399,RMVar_hsa_circ_83443,RMVar_hsa_circ_209403,RMVar_hsa_circ_42466,RMVar_hsa_circ_300574,RMVar_hsa_circ_300873,RMVar_hsa_circ_319670,RMVar_hsa_circ_42662,RMVar_hsa_circ_209402,RMVar_hsa_circ_209404,RMVar_hsa_circ_114957 116481 RMVar_ID_116481 Human_SNP_ID_842128549 m1A Human chr20 + 62201388 62201388 62201388 TGCCCATAACGGGGTGGCCCTGCCGCTGACTCAGGTCTCCGCCATGCACGCGTGGACTCTCGGAT TGCCCATAACGGGGTGGCCCTGCCGCTGACTCGGGTCTCCGCCATGCACGCGTGGACTCTCGGAT A G MTG2 Ensembl:ENSG00000101181 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2151511 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26492364 GWAS_ID_10079,GWAS_ID_10080,GWAS_ID_10081,GWAS_ID_10082,GWAS_ID_10083 116482 RMVar_ID_116482 Human_SNP_ID_842130635 m1A Human chr20 - 2659577 2659577 2659577 GTTTCTTCCTGTCCATATCCACAGTCTTGAGTATCACTCCAGCATGATCGCAGATGCGGTGAAGA GTTTCTTCCTGTCCATATCCACAGTCTTGAGTGTCACTCCAGCATGATCGCAGATGCGGTGAAGA T C IDH3B Ensembl:ENSG00000101365 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2659526..2659600 32194978 MeRIP-seq:(Medium) rs1568547187 Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_1927280,Human_RBP_ID_3960021,Human_RBP_ID_5382835,Human_RBP_ID_19003682 Human_Splice_Rec_2055270,Human_Splice_Rec_2055271,Human_Splice_Rec_2055278,Human_Splice_Rec_2055279,Human_Splice_Rec_2055300,Human_Splice_Rec_2055301,Human_Splice_Rec_2055322,Human_Splice_Rec_2055323,Human_Splice_Rec_2055344,Human_Splice_Rec_2055345,Human_Splice_Rec_2055366,Human_Splice_Rec_2055367,Human_Splice_Rec_2055374,Human_Splice_Rec_2055375,Human_Splice_Rec_2055396,Human_Splice_Rec_2055397,Human_Splice_Rec_2055400 RMVar_hsa_circ_88903,RMVar_hsa_circ_93887,RMVar_hsa_circ_105929,RMVar_hsa_circ_124535,RMVar_hsa_circ_114567,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_208326,RMVar_hsa_circ_208330,RMVar_hsa_circ_208332,RMVar_hsa_circ_83240,RMVar_hsa_circ_208333,RMVar_hsa_circ_208331,RMVar_hsa_circ_208328,RMVar_hsa_circ_208329,RMVar_hsa_circ_208327,RMVar_hsa_circ_21850,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_63077,RMVar_hsa_circ_208335 116483 RMVar_ID_116483 Human_SNP_ID_842137140 m1A Human chr20 - 17494323 17494323 17494323 TGTGCCATGGTCACACCCGGTGCAGAGGAACCATCTATACCTGAGCCTCCAAAGCCTGCGGCTGA TGTGCCATGGTCACACCCGGTGCAGAGGAACCGTCTATACCTGAGCCTCCAAAGCCTGCGGCTGA T C BFSP1 Ensembl:ENSG00000125864 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6080718 Functional Loss SNV ICGC 33..33 33 COCA 5 - GWAS_ID_9329,GWAS_ID_9330,GWAS_ID_9331,GWAS_ID_9332 116484 RMVar_ID_116484 Human_SNP_ID_842138268 m1A Human chr20 + 43673895 43673893 43673896 GGATAGCAAGTGCAAGGTCAAATGGACCCATGAGGAGGTGAGTGCCATGGGGAAGAGAGGGTTGA GGATAGCAAGTGCAAGGTCAAATGGACCCAT___GAGGTGAGTGCCATGGGGAAGAGAGGGTTGA TGAG T MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:43673743..43673995 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_925883,Human_RBP_ID_8854944,Human_RBP_ID_19005860,Human_RBP_ID_23005201,Human_RBP_ID_26343024 Human_Splice_Rec_2086268,Human_Splice_Rec_2086269,Human_Splice_Rec_2086292,Human_Splice_Rec_2086293 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210272,RMVar_hsa_circ_346978,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_349961,RMVar_hsa_circ_374244,RMVar_hsa_circ_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_210271 116485 RMVar_ID_116485 Human_SNP_ID_842147780 m1A Human chr20 + 63942321 63942321 63942321 CGTGACAGCGGCAGGGAAAGGGGCGGGGCCGGAAATGGGGTGTGGCAGGGCAGAAAAGAGGCGTG CGTGACAGCGGCAGGGAAAGGGGCGGGGCCGGGAATGGGGTGTGGCAGGGCAGAAAAGAGGCGTG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:63942276..63942649;chr20:63942276..63942626;chr20:63942276..63942489;chr20:63942271..63942456 26863196 MeRIP-seq:(Medium) rs2427570 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 3 oesophagus 116486 RMVar_ID_116486 Human_SNP_ID_842148592 m1A Human chr20 - 63707091 63707091 63707091 ACACTGACCTATGTTGGGGTGCCCAGGGCAGGATGTACACGCTGCTGTCGGGCTTGTACAAGTAC ACACTGACCTATGTTGGGGTGCCCAGGGCAGGGTGTACACGCTGCTGTCGGGCTTGTACAAGTAC T C ARFRP1 Ensembl:ENSG00000101246 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:63706966..63707562;chr20:63706965..63707498 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_4657665,Human_RBP_ID_5200834,Human_RBP_ID_5323081,Human_RBP_ID_5384275,Human_RBP_ID_18495465,Human_RBP_ID_19107125,Human_RBP_ID_22549582,Human_RBP_ID_22671183,Human_RBP_ID_22743761 Human_Splice_Rec_2104739,Human_Splice_Rec_2104752,Human_Splice_Rec_2104753,Human_Splice_Rec_2104766,Human_Splice_Rec_2104767,Human_Splice_Rec_2104776,Human_Splice_Rec_2104777,Human_Splice_Rec_2104796,Human_Splice_Rec_2104797,Human_Splice_Rec_2104810,Human_Splice_Rec_2104811,Human_Splice_Rec_2104822,Human_Splice_Rec_2104823 116487 RMVar_ID_116487 Human_SNP_ID_842162969 m1A Human chr20 + 32311034 32311034 32311034 GATAAGGATGATTACTGGCGGGAACAGCAAGAAAAACTGGAGATTGAGAAGCGGGCCATTGTAGA GATAAGGATGATTACTGGCGGGAACAGCAAGAGAAACTGGAGATTGAGAAGCGGGCCATTGTAGA A G KIF3B Ensembl:ENSG00000101350 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:32310730..32316300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_9430979,Human_RBP_ID_23899295 RMVar_hsa_circ_44469,RMVar_hsa_circ_319241,RMVar_hsa_circ_346622,RMVar_hsa_circ_209281 116488 RMVar_ID_116488 Human_SNP_ID_842163787 m1A Human chr20 - 25221335 25221335 25221335 CGCAGAAACCAACAGGCAGCAACCCTCCCCGTACCTGCTTTCTGCCCTGAAACCCTGTACGTGAC CGCAGAAACCAACAGGCAGCAACCCTCCCCGTTCCTGCTTTCTGCCCTGAAACCCTGTACGTGAC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25221296..25221379 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 6 kidney 116489 RMVar_ID_116489 Human_SNP_ID_842171893 m1A Human chr20 + 58898952 58898952 58898952 CTTTCAATCTCTCTTTAAAAGGGGCGGCGAAGAGGACCCGCAGGCTGCAAGGAGCAACAGCGATG CTTTCAATCTCTCTTTAAAAGGGGCGGCGAAGGGGACCCGCAGGCTGCAAGGAGCAACAGCGATG A G GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:58898926..58899000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung non_small_cell_carcinoma 11 lung Human_RBP_ID_62034,Human_RBP_ID_244154,Human_RBP_ID_778528,Human_RBP_ID_831170,Human_RBP_ID_2691816,Human_RBP_ID_5201248,Human_RBP_ID_14155217,Human_RBP_ID_23913558,Human_RBP_ID_24380404 Human_Splice_Rec_2098136,Human_Splice_Rec_2098137,Human_Splice_Rec_2098160,Human_Splice_Rec_2098161,Human_Splice_Rec_2098166,Human_Splice_Rec_2098190,Human_Splice_Rec_2098191,Human_Splice_Rec_2098214,Human_Splice_Rec_2098215,Human_Splice_Rec_2098252,Human_Splice_Rec_2098253,Human_Splice_Rec_2098282,Human_Splice_Rec_2098292,Human_Splice_Rec_2098293,Human_Splice_Rec_2098298,Human_Splice_Rec_2098299,Human_Splice_Rec_2098324,Human_Splice_Rec_2098325,Human_Splice_Rec_2098372,Human_Splice_Rec_2098373,Human_Splice_Rec_2098400,Human_Splice_Rec_2098401,Human_Splice_Rec_2098416,Human_Splice_Rec_2098424,Human_Splice_Rec_2098425,Human_Splice_Rec_2098430,Human_Splice_Rec_2098431,Human_Splice_Rec_2098452,Human_Splice_Rec_2098453,Human_Splice_Rec_2098482,Human_Splice_Rec_2098483,Human_Splice_Rec_2098498,Human_Splice_Rec_2098499,Human_Splice_Rec_2098528,Human_Splice_Rec_2098544,Human_Splice_Rec_2098545,Human_Splice_Rec_2098556,Human_Splice_Rec_2098557,Human_Splice_Rec_2098574,Human_Splice_Rec_2098575,Human_Splice_Rec_2098612,Human_Splice_Rec_2098656,Human_Splice_Rec_2098657,Human_Splice_Rec_2098680,Human_Splice_Rec_2098724,Human_Splice_Rec_2098725,Human_Splice_Rec_2098740,Human_Splice_Rec_2098741,Human_Splice_Rec_2098790,Human_Splice_Rec_2098791,Human_Splice_Rec_2098800,Human_Splice_Rec_2098801,Human_Splice_Rec_2098821 Human_miRNA_ID_1192304,Human_miRNA_ID_2571500,Human_miRNA_ID_3045236 RMVar_hsa_circ_14526,RMVar_hsa_circ_278184,RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_70998,RMVar_hsa_circ_344347,RMVar_hsa_circ_211085,RMVar_hsa_circ_211086,RMVar_hsa_circ_374022,RMVar_hsa_circ_211087 116490 RMVar_ID_116490 Human_SNP_ID_842179764 m1A Human chr20 + 422213 422213 422213 CTTCATTGACAACACCTACTCGTGCTCGGGCAAGCTGCTGGAGAGGGAGATCAAGGCGGTAAGGC CTTCATTGACAACACCTACTCGTGCTCGGGCAGGCTGCTGGAGAGGGAGATCAAGGCGGTAAGGC A G RBCK1 Ensembl:ENSG00000125826 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:417588..427322 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 4 head and neck Human_RBP_ID_9388453,Human_RBP_ID_17972062,Human_RBP_ID_19004889,Human_RBP_ID_27297258 Human_Splice_Rec_2052698,Human_Splice_Rec_2052699,Human_Splice_Rec_2052718,Human_Splice_Rec_2052719,Human_Splice_Rec_2052738,Human_Splice_Rec_2052739,Human_Splice_Rec_2052768,Human_Splice_Rec_2052769,Human_Splice_Rec_2052790,Human_Splice_Rec_2052791,Human_Splice_Rec_2052812,Human_Splice_Rec_2052813,Human_Splice_Rec_2052833,Human_Splice_Rec_2052835 RMVar_hsa_circ_208252,RMVar_hsa_circ_313990,RMVar_hsa_circ_330363 116491 RMVar_ID_116491 Human_SNP_ID_842181220 m1A Human chr20 + 63742451 63742451 63742451 ACGGGCTGTCCAGCCTGACTCCAGTGTCCCCCACGGCCTCCATGCCGCCTGCCTTCCCCCGCCTG ACGGGCTGTCCAGCCTGACTCCAGTGTCCCCCCCGGCCTCCATGCCGCCTGCCTTCCCCCGCCTG A C SLC2A4RG Ensembl:ENSG00000125520 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:63742300..63742625 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 1 lung Human_RBP_ID_568800,Human_RBP_ID_4657766,Human_RBP_ID_18777239 116492 RMVar_ID_116492 Human_SNP_ID_842200853 m1A Human chr20 - 58828997 58828997 58828997 GGGGCCAGGAGCTCTGCCATGTTGAGTGGGGCAGTGGGGCCAGGAGCTCTGCCATGTTGAGTGGG GGGGCCAGGAGCTCTGCCATGTTGAGTGGGGCGGTGGGGCCAGGAGCTCTGCCATGTTGAGTGGG T C GNAS-AS1 Ensembl:ENSG00000235590 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:58828996..58829248 26863196 MeRIP-seq:(Medium) rs866433998 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_7016934 116493 RMVar_ID_116493 Human_SNP_ID_842201024 m1A Human chr20 - 63590421 63590421 63590421 TGGGCAAGGGTTCCCTTCAGGCGCCCCCCGCCAGCTCCCCGGCCTCCCCGCTGCTCGGGGGATAC TGGGCAAGGGTTCCCTTCAGGCGCCCCCCGCCGGCTCCCCGGCCTCCCCGCTGCTCGGGGGATAC T C GMEB2 Ensembl:ENSG00000101216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63590370..63590448 26863196 MeRIP-seq:(Medium) rs1416892016 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_22260736 Human_miRNA_ID_2147550,Human_miRNA_ID_2988977,Human_miRNA_ID_3022679 RMVar_hsa_circ_101160,RMVar_hsa_circ_211325 116494 RMVar_ID_116494 Human_SNP_ID_842208452 m1A Human chr20 + 25339315 25339315 25339315 GGAATGGCAATGTACAACCCCAAAACACAGAAAAGTATCTTCCTCAGGCGCAACCACACGCCCTT GGAATGGCAATGTACAACCCCAAAACACAGAACAGTATCTTCCTCAGGCGCAACCACACGCCCTT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:25339264..25339634 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116495 RMVar_ID_116495 Human_SNP_ID_842228402 m1A Human chr20 - 63489013 63489013 63489013 TGACCGGCGCTCTGGCAAGAAGCTGGAGGACAACCCCAAGTCCCTGAAGTCTGGAGACGCGGCCA TGACCGGCGCTCTGGCAAGAAGCTGGAGGACATCCCCAAGTCCCTGAAGTCTGGAGACGCGGCCA T A EEF1A2 Ensembl:ENSG00000101210 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63488879..63489201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_63496,Human_RBP_ID_568640,Human_RBP_ID_27159050 Human_Splice_Rec_2103919,Human_Splice_Rec_2103933 116496 RMVar_ID_116496 Human_SNP_ID_842228408 m1A Human chr20 - 63489013 63489013 63489013 TGACCGGCGCTCTGGCAAGAAGCTGGAGGACAACCCCAAGTCCCTGAAGTCTGGAGACGCGGCCA TGACCGGCGCTCTGGCAAGAAGCTGGAGGACAGCCCCAAGTCCCTGAAGTCTGGAGACGCGGCCA T C EEF1A2 Ensembl:ENSG00000101210 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63488879..63489201 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_63496,Human_RBP_ID_568640,Human_RBP_ID_27159050 Human_Splice_Rec_2103919,Human_Splice_Rec_2103933 116497 RMVar_ID_116497 Human_SNP_ID_842239635 m1A Human chr20 + 59686752 59686752 59686752 TGGTTATGATGATGGTGGTGATGATGGTGATGATGATGGTGATGATGATGGTGATGATGATGGTG TGGTTATGATGATGGTGGTGATGATGGTGATGGTGATGGTGATGATGATGGTGATGATGATGGTG A G PHACTR3 Ensembl:ENSG00000087495 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:59686734..59686817 26863196 MeRIP-seq:(Medium) rs988195088 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116498 RMVar_ID_116498 Human_SNP_ID_842265617 m1A Human chr20 - 35002781 35002781 35002781 CCAGAGTGGGGAGGAAGATATGGGTGACCCCCACCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC CCAGAGTGGGGAGGAAGATATGGGTGACCCCCGCCCCCCATCTGTGAGCCAAGCCTCCCTTGTCC T C TRPC4AP Ensembl:ENSG00000100991 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs8501 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5323221,Human_RBP_ID_8857485,Human_RBP_ID_17970310,Human_RBP_ID_23212290,Human_RBP_ID_26493018 Human_miRNA_ID_2691194 GWAS_ID_14852,GWAS_ID_14853,GWAS_ID_14854,GWAS_ID_14855,GWAS_ID_14856,GWAS_ID_14857,GWAS_ID_14858,GWAS_ID_14859,GWAS_ID_14860,GWAS_ID_14861,GWAS_ID_14862,GWAS_ID_14863,GWAS_ID_14864,GWAS_ID_14865,GWAS_ID_14866,GWAS_ID_14867,GWAS_ID_14868,GWAS_ID_14869,GWAS_ID_14870,GWAS_ID_14871,GWAS_ID_14872,GWAS_ID_14873,GWAS_ID_14874,GWAS_ID_14875,GWAS_ID_14876,GWAS_ID_14877,GWAS_ID_14878,GWAS_ID_14879,GWAS_ID_14880,GWAS_ID_14881,GWAS_ID_14882,GWAS_ID_14883,GWAS_ID_14884,GWAS_ID_14885,GWAS_ID_14886,GWAS_ID_14887,GWAS_ID_14888,GWAS_ID_14889,GWAS_ID_14890,GWAS_ID_14891,GWAS_ID_14892,GWAS_ID_14893,GWAS_ID_14894,GWAS_ID_14895,GWAS_ID_14896,GWAS_ID_14897,GWAS_ID_14898,GWAS_ID_14899,GWAS_ID_14900,GWAS_ID_14901,GWAS_ID_14902,GWAS_ID_14903,GWAS_ID_14904,GWAS_ID_14905,GWAS_ID_14906,GWAS_ID_14907,GWAS_ID_14908,GWAS_ID_14909,GWAS_ID_14910,GWAS_ID_14911,GWAS_ID_14912,GWAS_ID_14913,GWAS_ID_14914,GWAS_ID_14915,GWAS_ID_14916,GWAS_ID_14917,GWAS_ID_14918,GWAS_ID_14919,GWAS_ID_14920,GWAS_ID_14921,GWAS_ID_14922,GWAS_ID_14923,GWAS_ID_14924,GWAS_ID_14925,GWAS_ID_14926,GWAS_ID_14927,GWAS_ID_14928,GWAS_ID_14929,GWAS_ID_14930,GWAS_ID_14931,GWAS_ID_14932,GWAS_ID_14933,GWAS_ID_14934,GWAS_ID_14935,GWAS_ID_14936,GWAS_ID_14937,GWAS_ID_14938,GWAS_ID_14939,GWAS_ID_14940,GWAS_ID_14941,GWAS_ID_14942,GWAS_ID_14943,GWAS_ID_14944,GWAS_ID_14945,GWAS_ID_14946,GWAS_ID_14947,GWAS_ID_14948,GWAS_ID_14949,GWAS_ID_14950,GWAS_ID_14951,GWAS_ID_14952,GWAS_ID_14953,GWAS_ID_14954,GWAS_ID_14955,GWAS_ID_14956,GWAS_ID_14957,GWAS_ID_14958,GWAS_ID_14959,GWAS_ID_14960,GWAS_ID_14961,GWAS_ID_14962,GWAS_ID_14963,GWAS_ID_14964,GWAS_ID_14965,GWAS_ID_14966,GWAS_ID_14967,GWAS_ID_14968,GWAS_ID_14969,GWAS_ID_14970,GWAS_ID_14971,GWAS_ID_14972,GWAS_ID_14973,GWAS_ID_14974,GWAS_ID_14975,GWAS_ID_14976,GWAS_ID_14977,GWAS_ID_14978,GWAS_ID_14979,GWAS_ID_14980,GWAS_ID_14981,GWAS_ID_14982,GWAS_ID_14983,GWAS_ID_14984,GWAS_ID_14985,GWAS_ID_14986,GWAS_ID_14987,GWAS_ID_14988,GWAS_ID_14989,GWAS_ID_14990,GWAS_ID_14991,GWAS_ID_14992,GWAS_ID_14993,GWAS_ID_14994,GWAS_ID_14995,GWAS_ID_14996,GWAS_ID_14997,GWAS_ID_14998,GWAS_ID_14999,GWAS_ID_15000,GWAS_ID_15001,GWAS_ID_15002,GWAS_ID_15003,GWAS_ID_15004,GWAS_ID_15005,GWAS_ID_15006,GWAS_ID_15007,GWAS_ID_15008,GWAS_ID_15009,GWAS_ID_15010,GWAS_ID_15011,GWAS_ID_15012,GWAS_ID_15013,GWAS_ID_15014,GWAS_ID_15015,GWAS_ID_15016,GWAS_ID_15017,GWAS_ID_15018,GWAS_ID_15019,GWAS_ID_15020,GWAS_ID_15021,GWAS_ID_15022,GWAS_ID_15023,GWAS_ID_15024,GWAS_ID_15025,GWAS_ID_15026,GWAS_ID_15027,GWAS_ID_15028,GWAS_ID_15029,GWAS_ID_15030,GWAS_ID_15031,GWAS_ID_15032,GWAS_ID_15033,GWAS_ID_15034,GWAS_ID_15035,GWAS_ID_15036,GWAS_ID_15037,GWAS_ID_15038,GWAS_ID_15039,GWAS_ID_15040,GWAS_ID_15041,GWAS_ID_15042,GWAS_ID_15043,GWAS_ID_15044,GWAS_ID_15045,GWAS_ID_15046,GWAS_ID_15047,GWAS_ID_15048,GWAS_ID_15049,GWAS_ID_15050,GWAS_ID_15051,GWAS_ID_15052,GWAS_ID_15053,GWAS_ID_15054,GWAS_ID_15055,GWAS_ID_15056,GWAS_ID_15057,GWAS_ID_15058,GWAS_ID_15059,GWAS_ID_15060,GWAS_ID_15061,GWAS_ID_15062,GWAS_ID_15063,GWAS_ID_15064,GWAS_ID_15065,GWAS_ID_15066,GWAS_ID_15067,GWAS_ID_15068,GWAS_ID_15069,GWAS_ID_15070,GWAS_ID_15071,GWAS_ID_15072,GWAS_ID_15073,GWAS_ID_15074,GWAS_ID_15075,GWAS_ID_15076,GWAS_ID_15077,GWAS_ID_15078,GWAS_ID_15079,GWAS_ID_15080,GWAS_ID_15081,GWAS_ID_15082,GWAS_ID_15083,GWAS_ID_15084,GWAS_ID_15085,GWAS_ID_15086,GWAS_ID_15087,GWAS_ID_15088,GWAS_ID_15089,GWAS_ID_15090,GWAS_ID_15091,GWAS_ID_15092,GWAS_ID_15093,GWAS_ID_15094,GWAS_ID_15095,GWAS_ID_15096,GWAS_ID_15097,GWAS_ID_15098,GWAS_ID_15099,GWAS_ID_15100,GWAS_ID_15101,GWAS_ID_15102,GWAS_ID_15103,GWAS_ID_15104,GWAS_ID_15105,GWAS_ID_15106,GWAS_ID_15107,GWAS_ID_15108,GWAS_ID_15109,GWAS_ID_15110,GWAS_ID_15111,GWAS_ID_15112,GWAS_ID_15113,GWAS_ID_15114,GWAS_ID_15115,GWAS_ID_15116,GWAS_ID_15117,GWAS_ID_15118,GWAS_ID_15119,GWAS_ID_15120,GWAS_ID_15121,GWAS_ID_15122,GWAS_ID_15123,GWAS_ID_15124,GWAS_ID_15125,GWAS_ID_15126,GWAS_ID_15127,GWAS_ID_15128,GWAS_ID_15129,GWAS_ID_15130,GWAS_ID_15131,GWAS_ID_15132,GWAS_ID_15133,GWAS_ID_15134,GWAS_ID_15135,GWAS_ID_15136,GWAS_ID_15137,GWAS_ID_15138,GWAS_ID_15139,GWAS_ID_15140,GWAS_ID_15141,GWAS_ID_15142,GWAS_ID_15143,GWAS_ID_15144,GWAS_ID_15145,GWAS_ID_15146,GWAS_ID_15147,GWAS_ID_15148,GWAS_ID_15149,GWAS_ID_15150,GWAS_ID_15151,GWAS_ID_15152,GWAS_ID_15153,GWAS_ID_15154,GWAS_ID_15155,GWAS_ID_15156,GWAS_ID_15157,GWAS_ID_15158,GWAS_ID_15159,GWAS_ID_15160,GWAS_ID_15161,GWAS_ID_15162,GWAS_ID_15163,GWAS_ID_15164,GWAS_ID_15165,GWAS_ID_15166,GWAS_ID_15167,GWAS_ID_15168,GWAS_ID_15169,GWAS_ID_15170,GWAS_ID_15171,GWAS_ID_15172,GWAS_ID_15173,GWAS_ID_15174,GWAS_ID_15175,GWAS_ID_15176,GWAS_ID_15177,GWAS_ID_15178,GWAS_ID_15179,GWAS_ID_15180,GWAS_ID_15181,GWAS_ID_15182,GWAS_ID_15183,GWAS_ID_15184,GWAS_ID_15185,GWAS_ID_15186,GWAS_ID_15187,GWAS_ID_15188,GWAS_ID_15189,GWAS_ID_15190,GWAS_ID_15191,GWAS_ID_15192,GWAS_ID_15193,GWAS_ID_15194,GWAS_ID_15195,GWAS_ID_15196,GWAS_ID_15197,GWAS_ID_15198,GWAS_ID_15199,GWAS_ID_15200,GWAS_ID_15201,GWAS_ID_15202,GWAS_ID_15203,GWAS_ID_15204,GWAS_ID_15205,GWAS_ID_15206,GWAS_ID_15207 RMVar_hsa_circ_99289,RMVar_hsa_circ_101021,RMVar_hsa_circ_209623,RMVar_hsa_circ_209624 116499 RMVar_ID_116499 Human_SNP_ID_842270908 m1A Human chr20 - 3233958 3233958 3233958 CAGATACCATCCAAGGGGTCACCGCCACAGTGACAGGGGTGCGGTACCAGCAGTCGTGGCTCTGC CAGATACCATCCAAGGGGTCACCGCCACAGTGTCAGGGGTGCGGTACCAGCAGTCGTGGCTCTGC T A SLC4A11 Ensembl:ENSG00000088836 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:3233929..3234020 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 8 oesophagus Human_Splice_Rec_2056296,Human_Splice_Rec_2056297,Human_Splice_Rec_2056334,Human_Splice_Rec_2056335,Human_Splice_Rec_2056372,Human_Splice_Rec_2056373,Human_Splice_Rec_2056410,Human_Splice_Rec_2056411,Human_Splice_Rec_2056448,Human_Splice_Rec_2056449,Human_Splice_Rec_2056486,Human_Splice_Rec_2056487,Human_Splice_Rec_2056522,Human_Splice_Rec_2056523 RMVar_hsa_circ_5556 116500 RMVar_ID_116500 Human_SNP_ID_842271958 m1A Human chr20 + 47651121 47651121 47651121 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCCACAGCAACAGCAACAGCAACAGCAGCAACAGC A C NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 116501 RMVar_ID_116501 Human_SNP_ID_842272696 m1A Human chr20 + 37521477 37521477 37521477 CGCGCCCCTAGAACCCGCAAGACTGCGTCGCGATTGCCGCTTCCCGGACCCGTCCTATTCCGATT CGCGCCCCTAGAACCCGCAAGACTGCGTCGCGGTTGCCGCTTCCCGGACCCGTCCTATTCCGATT A G NNAT Ensembl:ENSG00000053438 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:37521472..37521653 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116502 RMVar_ID_116502 Human_SNP_ID_842273258 m1A Human chr20 + 58678076 58678076 58678076 GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCATCTGATTTTAACCCATGGTTGAGACGTTCCAA GTTGAGAGTCACTGCAGGTGTTCTTTCATCCCGTCTGATTTTAACCCATGGTTGAGACGTTCCAA A G STX16-NPEPL1,STX16 Ensembl:ENSG00000254995,Ensembl:ENSG00000124222 Protein coding,Protein coding intron,3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6128397 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_1099734,Human_RBP_ID_8856526,Human_RBP_ID_14154359,Human_RBP_ID_17396245,Human_RBP_ID_17512474,Human_RBP_ID_22817880 GWAS_ID_8117,GWAS_ID_8118,GWAS_ID_8119,GWAS_ID_8120,GWAS_ID_8121,GWAS_ID_8122,GWAS_ID_8123,GWAS_ID_8124 RMVar_hsa_circ_211076,RMVar_hsa_circ_125383,RMVar_hsa_circ_264814 116503 RMVar_ID_116503 Human_SNP_ID_842286448 m1A Human chr20 - 63941711 63941711 63941711 ATCCCCAGGCTTGGGCAGCGGGGCGGGACGGGACAGCCAAGAGACACTGAGCCAGCTTTGCCCCC ATCCCCAGGCTTGGGCAGCGGGGCGGGACGGGGCAGCCAAGAGACACTGAGCCAGCTTTGCCCCC T C UCKL1 Ensembl:ENSG00000198276 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs817370 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5132313,Human_RBP_ID_17571998 GWAS_ID_10096 RMVar_hsa_circ_97929,RMVar_hsa_circ_33807,RMVar_hsa_circ_86952,RMVar_hsa_circ_211355,RMVar_hsa_circ_81811,RMVar_hsa_circ_211357,RMVar_hsa_circ_211358 116504 RMVar_ID_116504 Human_SNP_ID_842298696 m1A Human chr20 - 17659231 17659231 17659231 CCAGAATCAGGGCAAAAAGGCCGAGGGGGCCCAGAACCAGGGCAAGAAGGCCGAGGGGGCCCAGA CCAGAATCAGGGCAAAAAGGCCGAGGGGGCCCCGAACCAGGGCAAGAAGGCCGAGGGGGCCCAGA T G RRBP1 Ensembl:ENSG00000125844 Protein coding intron GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs202069077 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,head_neck squamous_cell_carcinoma,liver neoplasm,large_intestine adenocarcinoma 175 liver,head and neck,large intestine Human_miRNA_ID_865210 GWAS_ID_9333 RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_347823,RMVar_hsa_circ_356409 116505 RMVar_ID_116505 Human_SNP_ID_842301403 m1A Human chr20 + 58910079 58910079 58910079 TCCAGAATTTGCTCGCTACACTACTCCTGAGGATGGTGTGTATGGCTTCCACTCTTGCTGGCTGT TCCAGAATTTGCTCGCTACACTACTCCTGAGGTTGGTGTGTATGGCTTCCACTCTTGCTGGCTGT A T GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58909908..58910117 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 63 haematopoietic and lymphoid tissue Human_RBP_ID_18324018,Human_RBP_ID_19004476,Human_RBP_ID_19108951,Human_RBP_ID_22767409,Human_RBP_ID_27487604 Human_Splice_Rec_2098153,Human_Splice_Rec_2098181,Human_Splice_Rec_2098207,Human_Splice_Rec_2098231,Human_Splice_Rec_2098341,Human_Splice_Rec_2098363,Human_Splice_Rec_2098389,Human_Splice_Rec_2098449,Human_Splice_Rec_2098515,Human_Splice_Rec_2098603,Human_Splice_Rec_2098649,Human_Splice_Rec_2098673,Human_Splice_Rec_2098695,Human_Splice_Rec_2098717,Human_Splice_Rec_2098729,Human_Splice_Rec_2098817,Human_Splice_Rec_2098837,Human_Splice_Rec_2098855,Human_Splice_Rec_2098867,Human_Splice_Rec_2098897 RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_211086,RMVar_hsa_circ_14448,RMVar_hsa_circ_118782,RMVar_hsa_circ_211090 116506 RMVar_ID_116506 Human_SNP_ID_842301420 m1A Human chr20 + 58910079 58910079 58910079 TCCAGAATTTGCTCGCTACACTACTCCTGAGGATGGTGTGTATGGCTTCCACTCTTGCTGGCTGT TCCAGAATTTGCTCGCTACACTACTCCTGAGGGTGGTGTGTATGGCTTCCACTCTTGCTGGCTGT A G GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58909908..58910117 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 18 haematopoietic and lymphoid tissue Human_RBP_ID_18324018,Human_RBP_ID_19004476,Human_RBP_ID_19108951,Human_RBP_ID_22767409,Human_RBP_ID_27487604 Human_Splice_Rec_2098153,Human_Splice_Rec_2098181,Human_Splice_Rec_2098207,Human_Splice_Rec_2098231,Human_Splice_Rec_2098341,Human_Splice_Rec_2098363,Human_Splice_Rec_2098389,Human_Splice_Rec_2098449,Human_Splice_Rec_2098515,Human_Splice_Rec_2098603,Human_Splice_Rec_2098649,Human_Splice_Rec_2098673,Human_Splice_Rec_2098695,Human_Splice_Rec_2098717,Human_Splice_Rec_2098729,Human_Splice_Rec_2098817,Human_Splice_Rec_2098837,Human_Splice_Rec_2098855,Human_Splice_Rec_2098867,Human_Splice_Rec_2098897 RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_211086,RMVar_hsa_circ_14448,RMVar_hsa_circ_118782,RMVar_hsa_circ_211090 116507 RMVar_ID_116507 Human_SNP_ID_842301424 m1A Human chr20 + 58910079 58910079 58910079 TCCAGAATTTGCTCGCTACACTACTCCTGAGGATGGTGTGTATGGCTTCCACTCTTGCTGGCTGT TCCAGAATTTGCTCGCTACACTACTCCTGAGGCTGGTGTGTATGGCTTCCACTCTTGCTGGCTGT A C GNAS Ensembl:ENSG00000087460 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:58909908..58910117 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 18 haematopoietic and lymphoid tissue Human_RBP_ID_18324018,Human_RBP_ID_19004476,Human_RBP_ID_19108951,Human_RBP_ID_22767409,Human_RBP_ID_27487604 Human_Splice_Rec_2098153,Human_Splice_Rec_2098181,Human_Splice_Rec_2098207,Human_Splice_Rec_2098231,Human_Splice_Rec_2098341,Human_Splice_Rec_2098363,Human_Splice_Rec_2098389,Human_Splice_Rec_2098449,Human_Splice_Rec_2098515,Human_Splice_Rec_2098603,Human_Splice_Rec_2098649,Human_Splice_Rec_2098673,Human_Splice_Rec_2098695,Human_Splice_Rec_2098717,Human_Splice_Rec_2098729,Human_Splice_Rec_2098817,Human_Splice_Rec_2098837,Human_Splice_Rec_2098855,Human_Splice_Rec_2098867,Human_Splice_Rec_2098897 RMVar_hsa_circ_322191,RMVar_hsa_circ_290445,RMVar_hsa_circ_211086,RMVar_hsa_circ_14448,RMVar_hsa_circ_118782,RMVar_hsa_circ_211090 116508 RMVar_ID_116508 Human_SNP_ID_842308669 m1A Human chr20 + 13766865 13766865 13766865 TGAAAATCCATGTCCAAAAGCTCTTCCTTTTTAAACTTCCTGTTGAGCATTGTAATTCTTTCATG TGAAAATCCATGTCCAAAAGCTCTTCCTTTTTCAACTTCCTGTTGAGCATTGTAATTCTTTCATG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:13766740..13766872 26863196 MeRIP-seq:(Medium) rs777045761 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 116509 RMVar_ID_116509 Human_SNP_ID_842310659 m1A Human chr20 + 58651321 58651321 58651321 GGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGAAGGCCGGGGAGGCAGGCCCTGCTGTCTTCCTG GGGGATGGAGGGAGCCGGAGAAGAGGAGTGAGCAGGCCGGGGAGGCAGGCCCTGCTGTCTTCCTG A C STX16 Ensembl:ENSG00000124222 Protein coding 5'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr20:58651301..58651425;chr20:58651251..58652036 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_244816,Human_RBP_ID_779857,Human_RBP_ID_4665222,Human_RBP_ID_9389574,Human_RBP_ID_18422934,Human_RBP_ID_19006052,Human_RBP_ID_22259859,Human_RBP_ID_23004791,Human_RBP_ID_23119698,Human_RBP_ID_26343158,Human_RBP_ID_27819944 Human_Splice_Rec_2097685,Human_Splice_Rec_2097711,Human_Splice_Rec_2097805 116510 RMVar_ID_116510 Human_SNP_ID_842332871 m1A Human chr20 + 35466128 35466128 35466128 CGTGGTGAATAAAGCCCTTAGGGAAGATGTGGAAAAACTGACAGTGGACTGGAGCCGGGCCCGGG CGTGGTGAATAAAGCCCTTAGGGAAGATGTGGGAAAACTGACAGTGGACTGGAGCCGGGCCCGGG A G CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:35466077..35469927 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_924853,Human_RBP_ID_3960731,Human_RBP_ID_9389055,Human_RBP_ID_14084501,Human_RBP_ID_19004085,Human_RBP_ID_22081626,Human_RBP_ID_26343537 Human_Splice_Rec_2076064,Human_Splice_Rec_2076076,Human_Splice_Rec_2076092,Human_Splice_Rec_2076093,Human_Splice_Rec_2076122,Human_Splice_Rec_2076123,Human_Splice_Rec_2076190,Human_Splice_Rec_2076191,Human_Splice_Rec_2076202,Human_Splice_Rec_2076203,Human_Splice_Rec_2076224,Human_Splice_Rec_2076225 RMVar_hsa_circ_30687,RMVar_hsa_circ_67116,RMVar_hsa_circ_50287,RMVar_hsa_circ_317066,RMVar_hsa_circ_363819 116511 RMVar_ID_116511 Human_SNP_ID_842333523 m1A Human chr20 + 58991000 58991000 58991000 GCCTGCCAGGCTCTCGGGGCCATGCTGTCCAAAGGAGCCCTGAACCCTGCTGACATCACCGTCCT GCCTGCCAGGCTCTCGGGGCCATGCTGTCCAAGGGAGCCCTGAACCCTGCTGACATCACCGTCCT A G NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58990951..58991075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 1 head and neck Human_RBP_ID_7017280,Human_RBP_ID_14155839,Human_RBP_ID_17700860 Human_Splice_Rec_2098948,Human_Splice_Rec_2098949,Human_Splice_Rec_2098986,Human_Splice_Rec_2098987,Human_Splice_Rec_2099026,Human_Splice_Rec_2099027,Human_Splice_Rec_2099050,Human_Splice_Rec_2099051,Human_Splice_Rec_2099070,Human_Splice_Rec_2099071,Human_Splice_Rec_2099089,Human_Splice_Rec_2099097 Human_miRNA_ID_600794,Human_miRNA_ID_2224234,Human_miRNA_ID_2354519,Human_miRNA_ID_2487307,Human_miRNA_ID_3075674 RMVar_hsa_circ_12452,RMVar_hsa_circ_16165,RMVar_hsa_circ_27596,RMVar_hsa_circ_45609,RMVar_hsa_circ_211091,RMVar_hsa_circ_62354,RMVar_hsa_circ_120395,RMVar_hsa_circ_211095,RMVar_hsa_circ_115143,RMVar_hsa_circ_211094 116512 RMVar_ID_116512 Human_SNP_ID_842333568 m1A Human chr20 + 58991000 58991000 58991000 GCCTGCCAGGCTCTCGGGGCCATGCTGTCCAAAGGAGCCCTGAACCCTGCTGACATCACCGTCCT GCCTGCCAGGCTCTCGGGGCCATGCTGTCCAATGGAGCCCTGAACCCTGCTGACATCACCGTCCT A T NELFCD Ensembl:ENSG00000101158 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:58990951..58991075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_7017280,Human_RBP_ID_14155839,Human_RBP_ID_17700860 Human_Splice_Rec_2098948,Human_Splice_Rec_2098949,Human_Splice_Rec_2098986,Human_Splice_Rec_2098987,Human_Splice_Rec_2099026,Human_Splice_Rec_2099027,Human_Splice_Rec_2099050,Human_Splice_Rec_2099051,Human_Splice_Rec_2099070,Human_Splice_Rec_2099071,Human_Splice_Rec_2099089,Human_Splice_Rec_2099097 Human_miRNA_ID_600794,Human_miRNA_ID_2224234,Human_miRNA_ID_2354519,Human_miRNA_ID_2487307,Human_miRNA_ID_3075674 RMVar_hsa_circ_12452,RMVar_hsa_circ_16165,RMVar_hsa_circ_27596,RMVar_hsa_circ_45609,RMVar_hsa_circ_211091,RMVar_hsa_circ_62354,RMVar_hsa_circ_120395,RMVar_hsa_circ_211095,RMVar_hsa_circ_115143,RMVar_hsa_circ_211094 116513 RMVar_ID_116513 Human_SNP_ID_842338175 m1A Human chr20 - 17961755 17961755 17961755 CAAAATCTTAGTTTCTTAGGCAGTGGAATGAAACATAACAAAACAAAATCCCTAGAGGCTAGGAA CAAAATCTTAGTTTCTTAGGCAGTGGAATGAAGCATAACAAAACAAAATCCCTAGAGGCTAGGAA T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding exon,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6080918 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_559647,Human_RBP_ID_10010297,Human_RBP_ID_14043022,Human_RBP_ID_17967820,Human_RBP_ID_22999678,Human_RBP_ID_23895478,Human_RBP_ID_25628281 GWAS_ID_9334,GWAS_ID_9335,GWAS_ID_9336,GWAS_ID_9337,GWAS_ID_9338,GWAS_ID_9339,GWAS_ID_9340,GWAS_ID_9341,GWAS_ID_9342,GWAS_ID_9343,GWAS_ID_9344,GWAS_ID_9345,GWAS_ID_9346,GWAS_ID_9347,GWAS_ID_9348 116514 RMVar_ID_116514 Human_SNP_ID_842343800 m1A Human chr20 + 62658751 62658751 62658751 ACCTGATTGGAGGTGCCCTGCTGAATATCTACACGGAAATGGGCCGACGGTGAGTGGCCGCGCAC ACCTGATTGGAGGTGCCCTGCTGAATATCTACCCGGAAATGGGCCGACGGTGAGTGGCCGCGCAC A C SLCO4A1 Ensembl:ENSG00000101187 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:62658701..62658750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_1932581,Human_RBP_ID_19006261,Human_RBP_ID_19109110 Human_Splice_Rec_2101938,Human_Splice_Rec_2101939,Human_Splice_Rec_2101960,Human_Splice_Rec_2101961,Human_Splice_Rec_2101976,Human_Splice_Rec_2101977 RMVar_hsa_circ_90950,RMVar_hsa_circ_5755,RMVar_hsa_circ_284567,RMVar_hsa_circ_211251 116515 RMVar_ID_116515 Human_SNP_ID_842351202 m1A Human chr20 - 45894898 45894898 45894898 ACCAGGAGGAAGCCCACGCCCTCGCACACCTGATGCCACATCCGCTTGAGTGGCAGGCGAGTGAA ACCAGGAGGAAGCCCACGCCCTCGCACACCTGGTGCCACATCCGCTTGAGTGGCAGGCGAGTGAA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:45894826..45894925 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus RMVar_hsa_circ_210410 116516 RMVar_ID_116516 Human_SNP_ID_842356120 m1A Human chr20 + 31709123 31709123 31709123 ACAGGTGCTCTGGGCCTCTCCCCATTAGGCCCACCTCTACCATCAACCATCCCTCTGTCCAGAGG ACAGGTGCTCTGGGCCTCTCCCCATTAGGCCCTCCTCTACCATCAACCATCCCTCTGTCCAGAGG A T BCL2L1-AS1 Ensembl:ENSG00000236559 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:31709119..31709290 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_8114339 116517 RMVar_ID_116517 Human_SNP_ID_842373406 m1A Human chr20 - 34077095 34077095 34077095 CTGCTGCCACCGCCACCGCCACCACCACTGCCACCGCCACCGCTGCCACCACCACCGCCGCCGCC CTGCTGCCACCGCCACCGCCACCACCACTGCCGCCGCCACCGCTGCCACCACCACCGCCGCCGCC T C - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr20:34077050..34077211 26863196 MeRIP-seq:(Medium) rs781060935 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder 116518 RMVar_ID_116518 Human_SNP_ID_842374976 m1A Human chr20 + 35473935 35473935 35473935 GCTGCGGCAGCAGCTGGAGGTGCTAGAGCAGGAGGCATGGCGCCTGCGAAGGGTAAATGTGGAGC GCTGCGGCAGCAGCTGGAGGTGCTAGAGCAGGGGGCATGGCGCCTGCGAAGGGTAAATGTGGAGC A G CEP250 Ensembl:ENSG00000126001 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:35473854..35473979;chr20:35473441..35475564 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_9354029,Human_RBP_ID_23119675 Human_Splice_Rec_2076106,Human_Splice_Rec_2076136,Human_Splice_Rec_2076216 RMVar_hsa_circ_30687,RMVar_hsa_circ_67116 116519 RMVar_ID_116519 Human_SNP_ID_842392967 m1A Human chr20 + 17641858 17641826 17641859 CGACAGCCGCATCTTCCTGTTCTGTGGCCAGCAGTTTTTCCTTCTCTTCCAGCTGGCGTTTCAGA C_________________________________TTTTTCCTTCTCTTCCAGCTGGCGTTTCAGA CGACAGCCGCATCTTCCTGTTCTGTGGCCAGCAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17641776..17641925 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 2..34 33 BRCA 1 - 116520 RMVar_ID_116520 Human_SNP_ID_842394705 m1A Human chr20 - 32436576 32436576 32436576 CCTGTAACATTGCTCTGATCACCCAGGGCCCGACCTGTCTGCTCTGGACCAAAGGAGATCACATT CCTGTAACATTGCTCTGATCACCCAGGGCCCGGCCTGTCTGCTCTGGACCAAAGGAGATCACATT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr20:32436527..32436656;chr20:32436488..32436691;chr20:32436476..32436675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 116521 RMVar_ID_116521 Human_SNP_ID_842431847 m1A Human chr20 + 63695388 63695388 63695388 GACCCAGAGCAAGATCTCGTCCTTCCTTAGACAGAGGCCAGCAGGGACTGTGGGGGCGGGCGGTG GACCCAGAGCAAGATCTCGTCCTTCCTTAGACGGAGGCCAGCAGGGACTGTGGGGGCGGGCGGTG A G RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding 3'UTR,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63693180..63696143 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_18167808 Human_Splice_Rec_2104246,Human_Splice_Rec_2104247,Human_Splice_Rec_2104312,Human_Splice_Rec_2104313,Human_Splice_Rec_2104384,Human_Splice_Rec_2104448,Human_Splice_Rec_2104449,Human_Splice_Rec_2104584,Human_Splice_Rec_2104602,Human_Splice_Rec_2104662,Human_Splice_Rec_2104663,Human_Splice_Rec_2104700,Human_Splice_Rec_2104701,Human_Splice_Rec_2104728 Human_miRNA_ID_2210970,Human_miRNA_ID_2513397,Human_miRNA_ID_3056216 RMVar_hsa_circ_91497,RMVar_hsa_circ_211330,RMVar_hsa_circ_340566 116522 RMVar_ID_116522 Human_SNP_ID_842432234 m1A Human chr20 + 56388196 56388196 56388196 GTCCTGAAATGCAGTTTTCTTTAGATCGGTCCATGATGCCTGAAAAGAAAAAGAAGAACCTTTAA GTCCTGAAATGCAGTTTTCTTTAGATCGGTCCCTGATGCCTGAAAAGAAAAAGAAGAACCTTTAA A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:56388151..56388225 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 10 uterus 116523 RMVar_ID_116523 Human_SNP_ID_842433088 m1A Human chr20 - 59034911 59034911 59034911 TGTTATTTTAAAAATACAACTATATTTTGGGTAGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG TGTTATTTTAAAAATACAACTATATTTTGGGTTGTTTTTTTTTTTTTTTTTTTGATAAGTTGGTG T A PRELID3B Ensembl:ENSG00000101166 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs894717498 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_567667,Human_RBP_ID_1027035,Human_RBP_ID_7017436,Human_RBP_ID_9118659,Human_RBP_ID_17396299,Human_RBP_ID_17975005,Human_RBP_ID_23284184,Human_RBP_ID_27703703 RMVar_hsa_circ_87142,RMVar_hsa_circ_55675,RMVar_hsa_circ_211105,RMVar_hsa_circ_84849,RMVar_hsa_circ_211104,RMVar_hsa_circ_211106,RMVar_hsa_circ_90966 116524 RMVar_ID_116524 Human_SNP_ID_842445464 m1A Human chr20 + 41061470 41061470 41061470 CACAAAGAACACAAGAAGGAGAAGGACCGGGAAAAGTCCAAGCATAGCAACAGGTAAGGGTGGAA CACAAAGAACACAAGAAGGAGAAGGACCGGGACAAGTCCAAGCATAGCAACAGGTAAGGGTGGAA A C TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:41061340..41061544;chr20:41028826..41092505 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 1 stomach Human_RBP_ID_564148,Human_RBP_ID_925774,Human_RBP_ID_24546661 Human_Splice_Rec_2083674,Human_Splice_Rec_2083675 Human_miRNA_ID_130605 RMVar_hsa_circ_210158,RMVar_hsa_circ_9481,RMVar_hsa_circ_353056,RMVar_hsa_circ_357648,RMVar_hsa_circ_339116,RMVar_hsa_circ_210159,RMVar_hsa_circ_210160 116525 RMVar_ID_116525 Human_SNP_ID_842461954 m1A Human chr20 + 18316298 18316298 18316298 GCCGGGGCTTCAGCCAGCAATCCAACCTCATCAGACACCAGAGGACGCACTCAGGCGAGAAGCCC GCCGGGGCTTCAGCCAGCAATCCAACCTCATCTGACACCAGAGGACGCACTCAGGCGAGAAGCCC A T ZNF133 Ensembl:ENSG00000125846 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:18316248..18316449 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 12 brain RMVar_hsa_circ_125956,RMVar_hsa_circ_208894,RMVar_hsa_circ_76967,RMVar_hsa_circ_208895,RMVar_hsa_circ_92467,RMVar_hsa_circ_96173,RMVar_hsa_circ_208898,RMVar_hsa_circ_208899 116526 RMVar_ID_116526 Human_SNP_ID_842466929 m1A Human chr20 + 45792014 45792014 45792014 GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCACTGGCGACGCCGAGCAGCCGCGGGGACCTAGC GAGTTGTGGGGGCCGGGGGCGCCATGGGAGCCTCTGGCGACGCCGAGCAGCCGCGGGGACCTAGC A T DNTTIP1 Ensembl:ENSG00000101457 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:45791951..45792143 26863196 MeRIP-seq:(Medium) rs753122969 Functional Loss SNV TCGA,ICGC 33..33 33 THCA 2 - Human_RBP_ID_244662,Human_RBP_ID_4659436 Human_Splice_Rec_2089223,Human_Splice_Rec_2089247,Human_Splice_Rec_2089255 116527 RMVar_ID_116527 Human_SNP_ID_842469397 m1A Human chr20 + 20017425 20017425 20017425 CGCGATGACCACGCTACGGGCCTTTACCTGCGACGACCTGTTCCGCTTCAACAACATGTGAGTGA CGCGATGACCACGCTACGGGCCTTTACCTGCGTCGACCTGTTCCGCTTCAACAACATGTGAGTGA A T NAA20 Ensembl:ENSG00000173418 Protein coding exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr20:20017326..20017475 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_1024985,Human_RBP_ID_1593605,Human_RBP_ID_4659688,Human_RBP_ID_6982938,Human_RBP_ID_8852900,Human_RBP_ID_17510731,Human_RBP_ID_18422837,Human_RBP_ID_22255854,Human_RBP_ID_23896184,Human_RBP_ID_26820712 Human_Splice_Rec_2064977,Human_Splice_Rec_2064989,Human_Splice_Rec_2064997,Human_Splice_Rec_2065007,Human_Splice_Rec_2065015 116528 RMVar_ID_116528 Human_SNP_ID_842490968 m1A Human chr20 - 3786442 3786442 3786442 AAGAGGCGACAGCTGACGTTCCGGGAGAAGTCACGGATCATCCAGGAGGTGGAGGAGAATCCGGA AAGAGGCGACAGCTGACGTTCCGGGAGAAGTCGCGGATCATCCAGGAGGTGGAGGAGAATCCGGA T C CENPB Ensembl:ENSG00000125817 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:3786178..3786749;chr20:3785980..3786754;chr20:3786052..3786738 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1597054,Human_RBP_ID_4646953,Human_RBP_ID_17971576,Human_RBP_ID_22506615 116529 RMVar_ID_116529 Human_SNP_ID_842494357 m1A Human chr20 + 62308721 62308721 62308721 CGCCAAGCCCGAGCAGAAAGAGGGCGACACGAAGGACAAGAAGGACGAAGAGGAGGACATGAGCC CGCCAAGCCCGAGCAGAAAGAGGGCGACACGAGGGACAAGAAGGACGAAGAGGAGGACATGAGCC A G ADRM1 Ensembl:ENSG00000130706 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:62308642..62308811 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1600167,Human_RBP_ID_1932563,Human_RBP_ID_5597075,Human_RBP_ID_27489065 Human_Splice_Rec_2101448,Human_Splice_Rec_2101464,Human_Splice_Rec_2101482 Human_miRNA_ID_2255769 RMVar_hsa_circ_101576,RMVar_hsa_circ_111727,RMVar_hsa_circ_211190,RMVar_hsa_circ_211191,RMVar_hsa_circ_94931,RMVar_hsa_circ_211197,RMVar_hsa_circ_87881,RMVar_hsa_circ_103573,RMVar_hsa_circ_211199,RMVar_hsa_circ_97223,RMVar_hsa_circ_211200,RMVar_hsa_circ_211201 116530 RMVar_ID_116530 Human_SNP_ID_842514548 m1A Human chr20 + 41420984 41420984 41420984 CCGTGAGATGCAATACCTCTGGCCTTTCCCCCATGCCTACTGCCATGGCTAAGTTTTCCTCCTCG CCGTGAGATGCAATACCTCTGGCCTTTCCCCCGTGCCTACTGCCATGGCTAAGTTTTCCTCCTCG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:41420933..41421033 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 116531 RMVar_ID_116531 Human_SNP_ID_842524821 m1A Human chr20 + 49891028 49891028 49891028 TGAAGTCTCAGGTCCGTGTTCCCGCAGGGCGCACATGCTTGGAGAGTCCTCAGCAGGGTAGCCGA TGAAGTCTCAGGTCCGTGTTCCCGCAGGGCGCCCATGCTTGGAGAGTCCTCAGCAGGGTAGCCGA A C SLC9A8 Ensembl:ENSG00000197818 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:49890981..49891096 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_267681,RMVar_hsa_circ_210813,RMVar_hsa_circ_103913 116532 RMVar_ID_116532 Human_SNP_ID_842530988 m1A Human chr20 + 11918501 11918501 11918501 ATATATTCCCCCGTAAAAAGCCAGCCAACTCCAGCAGCACCAGCGTCCAGCAGTACCACCAGCAG ATATATTCCCCCGTAAAAAGCCAGCCAACTCCCGCAGCACCAGCGTCCAGCAGTACCACCAGCAG A C BTBD3 Ensembl:ENSG00000132640 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:11918476..11918500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 8 lung Human_RBP_ID_8528261,Human_RBP_ID_9388638,Human_RBP_ID_17967355 Human_miRNA_ID_272964,Human_miRNA_ID_2052880 RMVar_hsa_circ_35627,RMVar_hsa_circ_109284,RMVar_hsa_circ_208733,RMVar_hsa_circ_208734,RMVar_hsa_circ_208735,RMVar_hsa_circ_208736,RMVar_hsa_circ_314247 116533 RMVar_ID_116533 Human_SNP_ID_842533587 m1A Human chr20 + 63708094 63708094 63708094 GGAGGAAGTGCCGATCGGCTGCTGGGGCGAAAAGGGGGCGCCGGGCCGCTCTAGCCGGTGAGGCC GGAGGAAGTGCCGATCGGCTGCTGGGGCGAAAGGGGGGCGCCGGGCCGCTCTAGCCGGTGAGGCC A G ZGPAT Ensembl:ENSG00000197114 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:63708051..63708280 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_4660637,Human_RBP_ID_5529296,Human_RBP_ID_18423253 Human_Splice_Rec_2104873,Human_Splice_Rec_2104885,Human_Splice_Rec_2104895,Human_Splice_Rec_2104907,Human_Splice_Rec_2104909,Human_Splice_Rec_2104921 116534 RMVar_ID_116534 Human_SNP_ID_842551706 m1A Human chr20 - 34710241 34710241 34710241 ATGAAGCTGCTCTGGTTCTTGGACCGGCGCGGACGGCTCTCGCGGGCTCGGTTCTGCCGCTGCAC ATGAAGCTGCTCTGGTTCTTGGACCGGCGCGGGCGGCTCTCGCGGGCTCGGTTCTGCCGCTGCAC T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:34710194..34710294 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116535 RMVar_ID_116535 Human_SNP_ID_842553235 m1A Human chr20 + 45894900 45894900 45894900 CACTCGCCTGCCACTCAAGCGGATGTGGCATCAGGTGTGCGAGGGCGTGGGCTTCCTCCTGGTGA CACTCGCCTGCCACTCAAGCGGATGTGGCATCGGGTGTGCGAGGGCGTGGGCTTCCTCCTGGTGA A G CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:45894859..45895075 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney Human_RBP_ID_9389386,Human_RBP_ID_17976980,Human_RBP_ID_19005928 Human_Splice_Rec_2089562,Human_Splice_Rec_2089563,Human_Splice_Rec_2089590,Human_Splice_Rec_2089591,Human_Splice_Rec_2089624,Human_Splice_Rec_2089625,Human_Splice_Rec_2089664,Human_Splice_Rec_2089665,Human_Splice_Rec_2089692,Human_Splice_Rec_2089693,Human_Splice_Rec_2089734,Human_Splice_Rec_2089735,Human_Splice_Rec_2089762,Human_Splice_Rec_2089763,Human_Splice_Rec_2089770,Human_Splice_Rec_2089771,Human_Splice_Rec_2089780,Human_Splice_Rec_2089781 RMVar_hsa_circ_14707,RMVar_hsa_circ_296311,RMVar_hsa_circ_19067,RMVar_hsa_circ_210408,RMVar_hsa_circ_11833,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000,RMVar_hsa_circ_64193 116536 RMVar_ID_116536 Human_SNP_ID_842558208 m1A Human chr20 + 34089791 34089790 34089792 GCTTGCCCGTGACAGCCTGGAAGCCGGTTTTGATACTGGCAACAGAACATCTAGAATGACAAGTT GCTTGCCCGTGACAGCCTGGAAGCCGGTTTTG__ACTGGCAACAGAACATCTAGAATGACAAGTT GAT G RALY Ensembl:ENSG00000125970 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:34089748..34089853 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 LUSC 1 - 116537 RMVar_ID_116537 Human_SNP_ID_842561639 m1A Human chr20 + 63697022 63697022 63697022 CCGCGCCACTACACGCAGTTCTGGAACTACCTAGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG CCGCGCCACTACACGCAGTTCTGGAACTACCTGGAGCGCTGCCGCTACTGCAACGTCCTCTGCGG A G RTEL1-TNFRSF6B,TNFRSF6B Ensembl:ENSG00000026036,Ensembl:ENSG00000243509 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:63697009..63697156 26863196 MeRIP-seq:(Medium) rs2738787 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,caecum adenocarcinoma,colon adenocarcinoma,COCA,central_nervous_system astrocytoma_Grade_III,large_intestine adenocarcinoma 8 caecum,large intestine,brain Clinvar_Rec_433 GWAS_ID_10089,GWAS_ID_10090,GWAS_ID_10091,GWAS_ID_10092,GWAS_ID_10093,GWAS_ID_10094,GWAS_ID_10095 RMVar_hsa_circ_91497,RMVar_hsa_circ_211330 116538 RMVar_ID_116538 Human_SNP_ID_842588685 m1A Human chr20 + 17616786 17616786 17616786 GGGGGCGCCTCTGGGGAGGAAGCTGGGGCCCCAGCTATGTCACCATCCTCTACGTGGCTCTTCAT GGGGGCGCCTCTGGGGAGGAAGCTGGGGCCCCGGCTATGTCACCATCCTCTACGTGGCTCTTCAT A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:17616680..17618665 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 116539 RMVar_ID_116539 Human_SNP_ID_842591404 m1A Human chr20 + 33438947 33438946 33438947 TCCCCATTCACAGACAGGATGGCATCCCCCACAAAAAGGGCCTCTGTCTGGTCAGCTGCCAATCC TCCCCATTCACAGACAGGATGGCATCCCCCAC_AAAAGGGCCTCTGTCTGGTCAGCTGCCAATCC CA C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:33438897..33439078 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 STAD 1 - 116540 RMVar_ID_116540 Human_SNP_ID_842591558 m1A Human chr20 - 17947533 17947531 17947534 CAAAGACGTCAAGTTGGCTGAGGCACACCAGCAGGAGTGCTGCCAGAAATTTGAACAACTTTCCG CAAAGACGTCAAGTTGGCTGAGGCACACCAG___GAGTGCTGCCAGAAATTTGAACAACTTTCCG CCTG C SNX5 Ensembl:ENSG00000089006 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:17947487..17948931 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 BRCA 1 - Human_RBP_ID_559597,Human_RBP_ID_1926296,Human_RBP_ID_4661114,Human_RBP_ID_6981599,Human_RBP_ID_8528868,Human_RBP_ID_9388752,Human_RBP_ID_14042212,Human_RBP_ID_17512816,Human_RBP_ID_22255607,Human_RBP_ID_22999618,Human_RBP_ID_25594157 Human_Splice_Rec_2063619,Human_Splice_Rec_2063643,Human_Splice_Rec_2063667,Human_Splice_Rec_2063693,Human_Splice_Rec_2063699,Human_Splice_Rec_2063717 Human_miRNA_ID_272898,Human_miRNA_ID_2052882,Human_miRNA_ID_2513311,Human_miRNA_ID_2709291,Human_miRNA_ID_3056130 RMVar_hsa_circ_90919,RMVar_hsa_circ_208861,RMVar_hsa_circ_101264,RMVar_hsa_circ_119050,RMVar_hsa_circ_208862,RMVar_hsa_circ_274458,RMVar_hsa_circ_367212,RMVar_hsa_circ_372839,RMVar_hsa_circ_208863,RMVar_hsa_circ_17983,RMVar_hsa_circ_280877,RMVar_hsa_circ_312646,RMVar_hsa_circ_365936,RMVar_hsa_circ_208864,RMVar_hsa_circ_324891,RMVar_hsa_circ_282969,RMVar_hsa_circ_274234,RMVar_hsa_circ_208865,RMVar_hsa_circ_208867,RMVar_hsa_circ_208868,RMVar_hsa_circ_208866 116541 RMVar_ID_116541 Human_SNP_ID_842599232 m1A Human chr20 + 47651121 47651119 47651122 GCAACAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAACAGCAACAGCAACAGCAGCAACAGC GCAACAGCAGCAGCAGCAGCAGCAGCAGCAG___CAGCAACAGCAACAGCAACAGCAGCAACAGC GCAA G NCOA3 Ensembl:ENSG00000124151 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs112826888 Functional Loss DEL ICGC 32..34 33 STAD 1 - RMVar_hsa_circ_31424,RMVar_hsa_circ_52883,RMVar_hsa_circ_32151,RMVar_hsa_circ_210542,RMVar_hsa_circ_376364 116542 RMVar_ID_116542 Human_SNP_ID_842604832 m1A Human chr20 + 396962 396962 396962 AGGAGACAATATTCCCTGCTCACAGAGATGACAAACTGGCATCCTTGAGCTGACAACACTTTTCC AGGAGACAATATTCCCTGCTCACAGAGATGACCAACTGGCATCCTTGAGCTGACAACACTTTTCC A C TRIB3 Ensembl:ENSG00000101255 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:396911..397260 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_563925,Human_RBP_ID_1597071,Human_RBP_ID_1929699,Human_RBP_ID_8533280,Human_RBP_ID_17281450,Human_RBP_ID_17395427,Human_RBP_ID_17511564,Human_RBP_ID_17971595,Human_RBP_ID_18773036 Human_miRNA_ID_2903237 RMVar_hsa_circ_76297,RMVar_hsa_circ_79100,RMVar_hsa_circ_123114,RMVar_hsa_circ_208243,RMVar_hsa_circ_208244,RMVar_hsa_circ_208247 116543 RMVar_ID_116543 Human_SNP_ID_842606740 m1A Human chr20 - 18560864 18560864 18560864 AGGAATACAAATAAATTATAATCTAAAGAGTTACATATAAAATGTCCTTGATTATTTGTTAAAAT AGGAATACAAATAAATTATAATCTAAAGAGTTGCATATAAAATGTCCTTGATTATTTGTTAAAAT T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:18560816..18560966 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 116544 RMVar_ID_116544 Human_SNP_ID_842607184 m1A Human chr20 - 52152661 52152661 52152661 TCGTTGGGCATCAGGTGCCCCAGGCGAACACCATCGTCCAGGCTGCCGCCGCTGCAGTGAACATC TCGTTGGGCATCAGGTGCCCCAGGCGAACACCTTCGTCCAGGCTGCCGCCGCTGCAGTGAACATC T A ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr20:52152610..52152840 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung RMVar_hsa_circ_85485,RMVar_hsa_circ_210966 116545 RMVar_ID_116545 Human_SNP_ID_842623982 m1A Human chr20 + 13733841 13733841 13733841 TTTTTGACCATCTCTTCTGCACTTTCTTTAAGACCTGAGGAAAAATCCAAATAGTTTAGCTTAAA TTTTTGACCATCTCTTCTGCACTTTCTTTAAGCCCTGAGGAAAAATCCAAATAGTTTAGCTTAAA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:13733799..13766847 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - 116546 RMVar_ID_116546 Human_SNP_ID_842648398 m1A Human chr20 - 3753739 3753739 3753739 GGGTCCCCCACTCCCCACCCCAAGCCACAGGGACTCCCACCAGGGTCTGGGAGAGGACGGAGCTG GGGTCCCCCACTCCCCACCCCAAGCCACAGGGGCTCCCACCAGGGTCTGGGAGAGGACGGAGCTG T C C20orf27 Ensembl:ENSG00000101220 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEPG2 cell line,total RNA rearranged at 60c;HEK293T,ALKBH3 KO chr20:3753576..3753999;chr20:3753645..3753800 26863196,26863410 MeRIP-seq:(Medium) rs9171 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_281405,Human_RBP_ID_5240032,Human_RBP_ID_9353995,Human_RBP_ID_18463244,Human_RBP_ID_26492858,Human_RBP_ID_27564524 Human_miRNA_ID_2210941 RMVar_hsa_circ_208493,RMVar_hsa_circ_114478,RMVar_hsa_circ_125446,RMVar_hsa_circ_88933,RMVar_hsa_circ_208494,RMVar_hsa_circ_208492 116547 RMVar_ID_116547 Human_SNP_ID_842656820 m1A Human chr20 - 32311070 32311070 32311070 AGCCTCATCTTCTCCTCTGCAACCAAGCTGTGATCCTCTACAATGGCCCGCTTCTCAATCTCCAG AGCCTCATCTTCTCCTCTGCAACCAAGCTGTGGTCCTCTACAATGGCCCGCTTCTCAATCTCCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr20:32310704..32316300;chr20:32310760..32316284 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma,large_intestine adenocarcinoma 4 head and neck,large intestine 116548 RMVar_ID_116548 Human_SNP_ID_842657349 m1A Human chr20 + 2657942 2657942 2657942 CCCCTGTCCTTCCCTTTAGGAGATGAGTGAAAAACCCAAAAAGAAGAAAAAGCAAAAGCCCCAGG CCCCTGTCCTTCCCTTTAGGAGATGAGTGAAACACCCAAAAAGAAGAAAAAGCAAAAGCCCCAGG A C NOP56 Ensembl:ENSG00000101361 Protein coding 3'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_925155,Human_RBP_ID_3960535,Human_RBP_ID_5119123,Human_RBP_ID_9347945,Human_RBP_ID_9388508,Human_RBP_ID_18167615,Human_RBP_ID_18321194,Human_RBP_ID_19107313,Human_RBP_ID_24379578,Human_RBP_ID_26342636,Human_RBP_ID_27819522 Human_Splice_Rec_2055122,Human_Splice_Rec_2055156,Human_Splice_Rec_2055218,Human_Splice_Rec_2055238,Human_Splice_Rec_2055248,Human_Splice_Rec_2055262,Human_Splice_Rec_2055264 Human_miRNA_ID_184256 116549 RMVar_ID_116549 Human_SNP_ID_842694648 m1A Human chr20 - 46406574 46406574 46406574 CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCAGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT CTGGAGGAGCCGCCGAGCGGAGACCCGGGAGCGGGAGCTGGGCCTAGGTCTGCGCCCTGGTGAGT T C ELMO2 Ensembl:ENSG00000062598 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs401379 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4659446,Human_RBP_ID_19005962 Human_Splice_Rec_2090709,Human_Splice_Rec_2090749,Human_Splice_Rec_2090803,Human_Splice_Rec_2090925,Human_Splice_Rec_2090951,Human_Splice_Rec_2090979,Human_Splice_Rec_2090995,Human_Splice_Rec_2091009 116550 RMVar_ID_116550 Human_SNP_ID_842704693 m1A Human chr20 + 35557479 35557479 35557479 CATCTACCACTCAGCACGAGCCATCCAGAAGAAAATTGATCTAGGGAAGACAACGTAGTCACCCT CATCTACCACTCAGCACGAGCCATCCAGAAGACAATTGATCTAGGGAAGACAACGTAGTCACCCT A C ERGIC3 Ensembl:ENSG00000125991 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_562625,Human_RBP_ID_1595702,Human_RBP_ID_1928583,Human_RBP_ID_17511255,Human_RBP_ID_18771724,Human_RBP_ID_20647550,Human_RBP_ID_22767315,Human_RBP_ID_22817233,Human_RBP_ID_26821327 Human_Splice_Rec_2076346,Human_Splice_Rec_2076372,Human_Splice_Rec_2076432,Human_Splice_Rec_2076528,Human_Splice_Rec_2076536,Human_Splice_Rec_2076542,Human_Splice_Rec_2076546 RMVar_hsa_circ_91347,RMVar_hsa_circ_118312,RMVar_hsa_circ_209705,RMVar_hsa_circ_80229,RMVar_hsa_circ_209708,RMVar_hsa_circ_116216,RMVar_hsa_circ_209710,RMVar_hsa_circ_127137,RMVar_hsa_circ_209711,RMVar_hsa_circ_209712 116551 RMVar_ID_116551 Human_SNP_ID_842705554 m1A Human chr20 - 25491437 25491437 25491437 CGGAGCGAGAGCTGTTCTGGGAGCAGGCCCACAGGCAGAGGGCCGCGCTGGAGTGGGACGTGGGG CGGAGCGAGAGCTGTTCTGGGAGCAGGCCCACCGGCAGAGGGCCGCGCTGGAGTGGGACGTGGGG T G NINL Ensembl:ENSG00000101004 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:25491388..25491559 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_925428,Human_RBP_ID_9390242,Human_RBP_ID_19005260,Human_RBP_ID_23005132 Human_Splice_Rec_2068142,Human_Splice_Rec_2068143,Human_Splice_Rec_2068186,Human_Splice_Rec_2068187,Human_Splice_Rec_2068225 RMVar_hsa_circ_116613,RMVar_hsa_circ_209162,RMVar_hsa_circ_55058,RMVar_hsa_circ_34148,RMVar_hsa_circ_97647,RMVar_hsa_circ_37100,RMVar_hsa_circ_209166,RMVar_hsa_circ_72409,RMVar_hsa_circ_61669,RMVar_hsa_circ_8424,RMVar_hsa_circ_353317,RMVar_hsa_circ_79648,RMVar_hsa_circ_209167,RMVar_hsa_circ_56253,RMVar_hsa_circ_366513 116552 RMVar_ID_116552 Human_SNP_ID_842740873 m1A Human chr20 + 63488386 63488386 63488386 CGCTCTTCTTCTCCACGTTCTTGATGACGCCTACGGCCACCGTCTGCCTCATGTCGCGCACGGCG CGCTCTTCTTCTCCACGTTCTTGATGACGCCTGCGGCCACCGTCTGCCTCATGTCGCGCACGGCG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:63488026..63488462;chr20:63488301..63488434 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain 116553 RMVar_ID_116553 Human_SNP_ID_842741480 m1A Human chr20 + 16380008 16380008 16380008 TCTCCGCAAGTAAATCCTTTAGCTTGTTCTCGATGTGGAAGCTGCGGCGTTTGAGGCTCTCCTCC TCTCCGCAAGTAAATCCTTTAGCTTGTTCTCGTTGTGGAAGCTGCGGCGTTTGAGGCTCTCCTCC A T - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr20:16379957..16380109 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 116554 RMVar_ID_116554 Human_SNP_ID_842746876 m1A Human chr20 - 17621508 17621508 17621508 CCTCCAAGTTGAGGGAGGCCGAGGAGACGCAGAGCACACTGCAGGCCGAGTGTGACCAGTACCGC CCTCCAAGTTGAGGGAGGCCGAGGAGACGCAGTGCACACTGCAGGCCGAGTGTGACCAGTACCGC T A RRBP1 Ensembl:ENSG00000125844 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr20:17621430..17621550;chr20:17621451..17621525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_4636587,Human_RBP_ID_9388706,Human_RBP_ID_22452909 Human_Splice_Rec_2063280,Human_Splice_Rec_2063281,Human_Splice_Rec_2063320,Human_Splice_Rec_2063321,Human_Splice_Rec_2063362,Human_Splice_Rec_2063363,Human_Splice_Rec_2063410,Human_Splice_Rec_2063411,Human_Splice_Rec_2063456,Human_Splice_Rec_2063457,Human_Splice_Rec_2063502,Human_Splice_Rec_2063503,Human_Splice_Rec_2063546,Human_Splice_Rec_2063547 RMVar_hsa_circ_59520,RMVar_hsa_circ_42625,RMVar_hsa_circ_62648 116555 RMVar_ID_116555 Human_SNP_ID_842752797 m1A Human chr20 - 3213350 3213350 3213350 TGGCGAACTGCCTCCTGACATTTCTGTATGGAAATCTCATCCGGCTCCCCCTGGTACTCCGGCAC TGGCGAACTGCCTCCTGACATTTCTGTATGGATATCTCATCCGGCTCCCCCTGGTACTCCGGCAC T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:3209587..3213367 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung 116556 RMVar_ID_116556 Human_SNP_ID_842761070 m1A Human chr20 + 63969536 63969536 63969536 GCCTCGCCACCCACCTGTCACCTGGGGCCGGGAGCGGGCGCGGGGCGCGGGCCTCGGCCTGGCCG GCCTCGCCACCCACCTGTCACCTGGGGCCGGGCGCGGGCGCGGGGCGCGGGCCTCGGCCTGGCCG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr20:63969532..63969633 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116557 RMVar_ID_116557 Human_SNP_ID_842763947 m1A Human chr20 + 2660460 2660460 2660460 CCCATCCTACACAAAGCCATGCCCCTCACATGATGTTGGCCTTGTGGACAGCAGTGACCTTGCCC CCCATCCTACACAAAGCCATGCCCCTCACATGCTGTTGGCCTTGTGGACAGCAGTGACCTTGCCC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:2660451..2660525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116558 RMVar_ID_116558 Human_SNP_ID_842770434 m1A Human chr20 - 59006397 59006397 59006397 ACTGGCGCAATGTGGATGGTGTCAACTATGCCAGCATCACCCGGAACCAGCACATCCCCCAATAC ACTGGCGCAATGTGGATGGTGTCAACTATGCCGGCATCACCCGGAACCAGCACATCCCCCAATAC T C CTSZ Ensembl:ENSG00000101160 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr20:59006349..59006500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_22506957 Human_Splice_Rec_2099116,Human_Splice_Rec_2099117,Human_Splice_Rec_2099126,Human_Splice_Rec_2099127,Human_Splice_Rec_2099133,Human_Splice_Rec_2099138 Human_miRNA_ID_272941 RMVar_hsa_circ_57119,RMVar_hsa_circ_302597,RMVar_hsa_circ_211101,RMVar_hsa_circ_81573,RMVar_hsa_circ_211102,RMVar_hsa_circ_372909,RMVar_hsa_circ_211103 116559 RMVar_ID_116559 Human_SNP_ID_842804883 m1A Human chr20 - 62937858 62937858 62937858 GCGTCGGCCCTCTGGCAAGATGGCTGCTGCGGAGGCGTTGGAGCGCGGAAATCTGGAACCGGGAT GCGTCGGCCCTCTGGCAAGATGGCTGCTGCGGTGGCGTTGGAGCGCGGAAATCTGGAACCGGGAT T A DIDO1 Ensembl:ENSG00000101191 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr20:62926459..62937902;chr20:62937649..62937878 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_244763,Human_RBP_ID_4656706,Human_RBP_ID_9389710,Human_RBP_ID_14164825,Human_RBP_ID_19006336,Human_RBP_ID_23005266,Human_RBP_ID_26342555 Human_Splice_Rec_2102371,Human_Splice_Rec_2102455 116560 RMVar_ID_116560 Human_SNP_ID_842807456 m1A Human chr20 - 49221517 49221517 49221517 TACGTCCCCTCCTTCTCAGTGAAAACGAAATCAGGGTTGAAATCAGCACTGCGGTTCTTCCCCAA TACGTCCCCTCCTTCTCAGTGAAAACGAAATCGGGGTTGAAATCAGCACTGCGGTTCTTCCCCAA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:49219443..49223409 32194978 MeRIP-seq:(Medium) rs1453637369 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 3 stomach 116561 RMVar_ID_116561 Human_SNP_ID_842823349 m1A Human chr20 - 34363351 34363351 34363351 GAGAACTGCCCCGAGTTCGCCCACGGGGGTTTACCGGGACTCGGGGCGGCGGCGACTCCTCAGTC GAGAACTGCCCCGAGTTCGCCCACGGGGGTTTGCCGGGACTCGGGGCGGCGGCGACTCCTCAGTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:34363329..34363449;chr20:34363330..34363473;chr20:34363330..34363500;chr20:34363324..34363491 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - 116562 RMVar_ID_116562 Human_SNP_ID_842825751 m1A Human chr20 - 63690376 63690373 63690376 GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAGAAGGGGCCAGGCGACTTGGCCTCGCTGACAGCA GGTCCAGACTCTTAGCTTTCCTGGTGGAGAAG___GGGCCAGGCGACTTGGCCTCGCTGACAGCA CCTT C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:63690104..63690388 32194978 MeRIP-seq:(Medium) rs771771098 Functional Loss DEL TCGA 33..35 33 COAD,STAD 2 - Clinvar_Rec_432 116563 RMVar_ID_116563 Human_SNP_ID_842845464 m1A Human chr20 - 21368455 21368455 21368455 TCCTGAGCCTCTTGGCATCACATGGCTATAAAAGGACCCAACACAAGAAAAAAAAATTGTATAGT TCCTGAGCCTCTTGGCATCACATGGCTATAAACGGACCCAACACAAGAAAAAAAAATTGTATAGT T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr20:21368451..21368500 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116564 RMVar_ID_116564 Human_SNP_ID_842852886 m1A Human chr20 - 60256544 60256544 60256544 CGGCTCTGACCATGTCATTACTCTATCTCCAAACCCATTTCTCCTGTCACTCAGATGCAACCCAA CGGCTCTGACCATGTCATTACTCTATCTCCAACCCCATTTCTCCTGTCACTCAGATGCAACCCAA T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:60256493..60256605 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116565 RMVar_ID_116565 Human_SNP_ID_842881070 m1A Human chr20 - 45813428 45813427 45813428 AGGGTCATCAGCTCCTGCTGTAGCCTGAAAAAAGAGTATTCGGGGTTACCTGGGAGTCTGGATGG AGGGTCATCAGCTCCTGCTGTAGCCTGAAAAA_GAGTATTCGGGGTTACCTGGGAGTCTGGATGG CT C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr20:45813426..45813475 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 CHOL 1 - 116566 RMVar_ID_116566 Human_SNP_ID_842907227 m1A Human chr20 - 41163802 41163802 41163802 CGTGTTGTGCGAGGAGGAGATCCAGTAGTGGGAAAGAGGGTTGTTCATGGTGTCCGGGCATACTG CGTGTTGTGCGAGGAGGAGATCCAGTAGTGGGGAAGAGGGTTGTTCATGGTGTCCGGGCATACTG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr20:41163751..41163850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 116567 RMVar_ID_116567 Human_SNP_ID_842907929 m1A Human chr20 - 3203362 3203362 3203362 TGAGGAGCTGGCAGGAGCAGGCCGGGTGGCCCAGCCTGGGCCCCTGGAGCCTGAGGAGCCGAGAG TGAGGAGCTGGCAGGAGCAGGCCGGGTGGCCCCGCCTGGGCCCCTGGAGCCTGAGGAGCCGAGAG T G DDRGK1 Ensembl:ENSG00000198171 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr20:3203326..3203425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_4641815,Human_RBP_ID_22452867 Human_Splice_Rec_2056160,Human_Splice_Rec_2056180 RMVar_hsa_circ_53842,RMVar_hsa_circ_364112 116568 RMVar_ID_116568 Human_SNP_ID_842907972 m1A Human chr20 - 62836335 62836335 62836335 TGTGAAAGCTGGAAAAGCCGGAAAAGCGACGTACCGGAACTCCCGGCTTCCCCGTGATGCCAGGA TGTGAAAGCTGGAAAAGCCGGAAAAGCGACGTGCCGGAACTCCCGGCTTCCCCGTGATGCCAGGA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr20:62836156..62836355;chr20:62836148..62836355 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116569 RMVar_ID_116569 Human_SNP_ID_842911525 m1A Human chr20 - 3758627 3758627 3758627 GAGTATCCGCTTTGCGGCAGGCCACGATGCAGAAGGATCCCACAGCCACGTCCACTTTGATGAGA GAGTATCCGCTTTGCGGCAGGCCACGATGCAGGAGGATCCCACAGCCACGTCCACTTTGATGAGA T C C20orf27 Ensembl:ENSG00000101220 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr20:3758576..3758734 26863196 MeRIP-seq:(Medium) rs920160078 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_1596975,Human_RBP_ID_1929642,Human_RBP_ID_3648454,Human_RBP_ID_4663497,Human_RBP_ID_9117051 Human_Splice_Rec_2057075,Human_Splice_Rec_2057082,Human_Splice_Rec_2057083,Human_Splice_Rec_2057092,Human_Splice_Rec_2057093,Human_Splice_Rec_2057102,Human_Splice_Rec_2057103 RMVar_hsa_circ_114478,RMVar_hsa_circ_208494,RMVar_hsa_circ_104708,RMVar_hsa_circ_208495,RMVar_hsa_circ_297004 116570 RMVar_ID_116570 Human_SNP_ID_809979898 m1A Human chr11 - 77339502 77339499 77339503 TTAATACCAGGCTGGGATTCTTAGGGGTTCTGACTTTTTTTTTTGTTCCACTACTAATGCAGTAT TTAATACCAGGCTGGGATTCTTAGGGGTTCT____TTTTTTTTTGTTCCACTACTAATGCAGTAT AAGTC A PAK1 Ensembl:ENSG00000149269 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:77339414..77339503 26863410 MeRIP-seq:(Medium) rs1323191243 Functional Loss DEL ICGC 32..35 33 PBCA 1 - RMVar_hsa_circ_10105,RMVar_hsa_circ_151878,RMVar_hsa_circ_80583,RMVar_hsa_circ_296024,RMVar_hsa_circ_300105,RMVar_hsa_circ_321147,RMVar_hsa_circ_319744,RMVar_hsa_circ_296574,RMVar_hsa_circ_291428,RMVar_hsa_circ_26103,RMVar_hsa_circ_151880,RMVar_hsa_circ_151882,RMVar_hsa_circ_151884,RMVar_hsa_circ_151885,RMVar_hsa_circ_151883,RMVar_hsa_circ_151881,RMVar_hsa_circ_96052,RMVar_hsa_circ_373317,RMVar_hsa_circ_151889,RMVar_hsa_circ_126302,RMVar_hsa_circ_151886,RMVar_hsa_circ_151887,RMVar_hsa_circ_116738,RMVar_hsa_circ_151888 116571 RMVar_ID_116571 Human_SNP_ID_809988964 m1A Human chr11 - 32098524 32098524 32098524 CCCAGCCCAGACTCTTCACTTATCTTACCAAAACCACAATTTCCTTCATATGTTCAAACTCTTCA CCCAGCCCAGACTCTTCACTTATCTTACCAAAGCCACAATTTCCTTCATATGTTCAAACTCTTCA T C AL078612.2 Ensembl:ENSG00000255252 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:32098423..32098573 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_5552851 116572 RMVar_ID_116572 Human_SNP_ID_809990620 m1A Human chr11 - 78174025 78174025 78174025 CTCCAATGGCAATCTCTCCTCCATCACCAGCCACTTGCAGGACCCCAACCACCTGACTCTGGACT CTCCAATGGCAATCTCTCCTCCATCACCAGCCGCTTGCAGGACCCCAACCACCTGACTCTGGACT T C KCTD21 Ensembl:ENSG00000188997 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:78173974..78174125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_27416444,Human_RBP_ID_27557423 116573 RMVar_ID_116573 Human_SNP_ID_809997232 m1A Human chr11 + 62579026 62579026 62579026 AGTCCAGCGATGGAGATTCTGGAGCCTTTGGGACTGGCTGTGGACAGAAATGAACTGAGTGAAAT AGTCCAGCGATGGAGATTCTGGAGCCTTTGGGGCTGGCTGTGGACAGAAATGAACTGAGTGAAAT A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62578866..62581192 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 2 head and neck 116574 RMVar_ID_116574 Human_SNP_ID_809999106 m1A Human chr11 + 32619778 32619778 32619778 GAAGGAGGAGGAGGAGATGAAGAAGGAGCAGAAGAAGCAGAAGAAGCAGGAGGAAAAGGAGGAGG GAAGGAGGAGGAGGAGATGAAGAAGGAGCAGACGAAGCAGAAGAAGCAGGAGGAAAAGGAGGAGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:32619727..32619849 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 116575 RMVar_ID_116575 Human_SNP_ID_810006813 m1A Human chr11 + 11958127 11958127 11958127 GGGTTTCTGCTTTAAAGGACTGACTTGCTATCACACAAAAGAGGCAGACTTGTAAACACAATGGG GGGTTTCTGCTTTAAAGGACTGACTTGCTATCGCACAAAAGAGGCAGACTTGTAAACACAATGGG A G USP47 Ensembl:ENSG00000170242 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1979687 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_miRNA_ID_321465,Human_miRNA_ID_1008572 GWAS_ID_6822,GWAS_ID_6823,GWAS_ID_6824,GWAS_ID_6825 116576 RMVar_ID_116576 Human_SNP_ID_810011744 m1A Human chr11 - 34916680 34916680 34916680 GCCCACAAGATAACGCAGCAGCCGCGGATCACAGCCCAGCCTCCAGGAGGCCGCCATCTTGACGG GCCCACAAGATAACGCAGCAGCCGCGGATCACGGCCCAGCCTCCAGGAGGCCGCCATCTTGACGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:34916464..34947604 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116577 RMVar_ID_116577 Human_SNP_ID_810013852 m1A Human chr11 - 65132950 65132950 65132950 CTTCACTCTTCTTCTCTTCCTCAAATGTTTCCACTGGCTGGCTGAGGACCGTGTGGACTTTGTGA CTTCACTCTTCTTCTCTTCCTCAAATGTTTCCGCTGGCTGGCTGAGGACCGTGTGGACTTTGTGA T C SYVN1 Ensembl:ENSG00000162298 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65132926..65132950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_750026,Human_RBP_ID_18432993,Human_RBP_ID_18972195,Human_RBP_ID_22433748,Human_RBP_ID_22753704,Human_RBP_ID_27413860 Human_Splice_Rec_1257255,Human_Splice_Rec_1257285,Human_Splice_Rec_1257315,Human_Splice_Rec_1257341,Human_Splice_Rec_1257363,Human_Splice_Rec_1257405,Human_Splice_Rec_1257421,Human_Splice_Rec_1257433,Human_Splice_Rec_1257443,Human_Splice_Rec_1257459,Human_Splice_Rec_1257469,Human_Splice_Rec_1257471 Human_miRNA_ID_883128,Human_miRNA_ID_2397735 RMVar_hsa_circ_2171,RMVar_hsa_circ_120755,RMVar_hsa_circ_368048,RMVar_hsa_circ_150585 116578 RMVar_ID_116578 Human_SNP_ID_810021698 m1A Human chr11 - 130122371 130122371 130122371 CGGTCCTCCACCACTTCCTCCCCTTCTTCCTCATCCTCATCATCCTCATCCACAGCTGCTTCTGT CGGTCCTCCACCACTTCCTCCCCTTCTTCCTCGTCCTCATCATCCTCATCCACAGCTGCTTCTGT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:130122272..130122558;chr11:130122301..130122475;chr11:130122301..130122450 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116579 RMVar_ID_116579 Human_SNP_ID_810033529 m1A Human chr11 - 64197539 64197539 64197539 CGGTTTTCTCTCCCCACTTCAATGGCCTTCTCACAAAGCTCCCGGCACTTATTGTAGTCGCCCTT CGGTTTTCTCTCCCCACTTCAATGGCCTTCTCTCAAAGCTCCCGGCACTTATTGTAGTCGCCCTT T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64197477..64197630 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 5 caecum,large intestine 116580 RMVar_ID_116580 Human_SNP_ID_810036971 m1A Human chr11 - 47580866 47580866 47580866 AAGTCAGCACTGGGATGACGCCATCAGGATGGATACAGACCTCTAACTCATTGAAGCAGGACACC AAGTCAGCACTGGGATGACGCCATCAGGATGGTTACAGACCTCTAACTCATTGAAGCAGGACACC T A - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:47580857..47581006 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine RMVar_hsa_circ_149587 116581 RMVar_ID_116581 Human_SNP_ID_810052402 m1A Human chr11 - 20367257 20367257 20367257 TTCCTTACCGCCCCAGCTTTCCCTCTGGTGGTACCCAGGCAACAGAATCCAACATCATGACCTTG TTCCTTACCGCCCCAGCTTTCCCTCTGGTGGTGCCCAGGCAACAGAATCCAACATCATGACCTTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:20367206..20367282 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 116582 RMVar_ID_116582 Human_SNP_ID_810053696 m1A Human chr11 + 76796260 76796260 76796260 CTTGCCCCTGCGCTACCTGAGCCTGGATGGGAACCCTCTAGCTGTCATTGGTCCGGGTGCCTTCG CTTGCCCCTGCGCTACCTGAGCCTGGATGGGATCCCTCTAGCTGTCATTGGTCCGGGTGCCTTCG A T TSKU Ensembl:ENSG00000182704 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:76796212..76796562 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung mixed_adenosquamous_carcinoma 3 lung Human_RBP_ID_5110605,Human_RBP_ID_22033676,Human_RBP_ID_27207348,Human_RBP_ID_27416329 RMVar_hsa_circ_100357,RMVar_hsa_circ_151860 116583 RMVar_ID_116583 Human_SNP_ID_810056560 m1A Human chr11 + 64232793 64232793 64232793 GGGGCCCCAGTTGAGGCAGCAGCAACACAAACAAAACAAACAAGTGCTGGGGTACTGCCTCCTCC GGGGCCCCAGTTGAGGCAGCAGCAACACAAACTAAACAAACAAGTGCTGGGGTACTGCCTCCTCC A T DNAJC4 Ensembl:ENSG00000110011 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64232743..64232865 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_Splice_Rec_1252868,Human_Splice_Rec_1252869,Human_Splice_Rec_1252884,Human_Splice_Rec_1252890,Human_Splice_Rec_1252891,Human_Splice_Rec_1252894,Human_Splice_Rec_1252900,Human_Splice_Rec_1252904,Human_Splice_Rec_1252908,Human_Splice_Rec_1252909,Human_Splice_Rec_1252916 116584 RMVar_ID_116584 Human_SNP_ID_810063634 m1A Human chr11 + 68262420 68262420 68262420 TTGGCAACGCGCTGCTCTTTGGCACTTGTGCGAGGGCTGTGCTGAGAGATGGATGCCCAGTGGCG TTGGCAACGCGCTGCTCTTTGGCACTTGTGCGCGGGCTGTGCTGAGAGATGGATGCCCAGTGGCG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68262370..68262519 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 116585 RMVar_ID_116585 Human_SNP_ID_810064362 m1A Human chr11 + 117390833 117390833 117390833 AGCCATTGAGGAGGAGGAGGCCCGGATGAGAGAGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAG AGCCATTGAGGAGGAGGAGGCCCGGATGAGAGCGGAGGAAAGCCAGAGGCTATCCTGGCTCCGAG A C CEP164 Ensembl:ENSG00000110274 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:117390784..117390889 26863196 MeRIP-seq:(Medium) rs150261648 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_226374,Human_RBP_ID_26319253 Human_Splice_Rec_1302232,Human_Splice_Rec_1302233,Human_Splice_Rec_1302314,Human_Splice_Rec_1302315,Human_Splice_Rec_1302362,Human_Splice_Rec_1302363,Human_Splice_Rec_1302402,Human_Splice_Rec_1302403,Human_Splice_Rec_1302406,Human_Splice_Rec_1302407 RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_153310,RMVar_hsa_circ_87554,RMVar_hsa_circ_93331,RMVar_hsa_circ_117454,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_153314,RMVar_hsa_circ_113876,RMVar_hsa_circ_153315,RMVar_hsa_circ_153316,RMVar_hsa_circ_153317,RMVar_hsa_circ_40624,RMVar_hsa_circ_102113,RMVar_hsa_circ_26636,RMVar_hsa_circ_153320,RMVar_hsa_circ_329540,RMVar_hsa_circ_153321 116586 RMVar_ID_116586 Human_SNP_ID_810064589 m1A Human chr11 - 119665022 119665019 119665022 TGCAGTACCCCGACGACTCAGACGACGAGAAGAAGGCCGGCCCACTGGGTGGAAGCAGCTATGAG TGCAGTACCCCGACGACTCAGACGACGAGAAG___GCCGGCCCACTGGGTGGAAGCAGCTATGAG CCTT C NECTIN1 Ensembl:ENSG00000110400 Protein coding intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:119664999..119665132 26863196 MeRIP-seq:(Medium) rs1022251180 Functional Loss DEL TCGA 33..35 33 UCEC,LUAD 2 - RMVar_hsa_circ_153562 116587 RMVar_ID_116587 Human_SNP_ID_810070210 m1A Human chr11 + 118409088 118409088 118409088 AGAGATTATAGGCAAGCGGGGCATCATTGGCTATGATGTTTGAAGACCAATCTTTAACATCTGAT AGAGATTATAGGCAAGCGGGGCATCATTGGCTGTGATGTTTGAAGACCAATCTTTAACATCTGAT A G AP001267.5,ATP5MG Ensembl:ENSG00000285827,Ensembl:ENSG00000167283 Protein coding,Protein coding intron,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118409038..118409119 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_389821,Human_RBP_ID_809165,Human_RBP_ID_1454414,Human_RBP_ID_1775902,Human_RBP_ID_5110632,Human_RBP_ID_6048510,Human_RBP_ID_11536172,Human_RBP_ID_17648478,Human_RBP_ID_17804798,Human_RBP_ID_22434848,Human_RBP_ID_23207109,Human_RBP_ID_23488914,Human_RBP_ID_24458865,Human_RBP_ID_26886138 Human_Splice_Rec_1304088,Human_Splice_Rec_1304094,Human_Splice_Rec_1304102,Human_Splice_Rec_1304106,Human_Splice_Rec_1304114,Human_Splice_Rec_1304118 Human_miRNA_ID_2668150,Human_miRNA_ID_2767482 RMVar_hsa_circ_153355,RMVar_hsa_circ_128113,RMVar_hsa_circ_153356 116588 RMVar_ID_116588 Human_SNP_ID_810077679 m1A Human chr11 - 64371333 64371333 64371333 AGCTTCTGCTTCCGCCGCTTGGCCAGGGGTGCATTCTCCACGCTCTTCAGGAAGAAGCCCTCCCG AGCTTCTGCTTCCGCCGCTTGGCCAGGGGTGCGTTCTCCACGCTCTTCAGGAAGAAGCCCTCCCG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64371276..64371500 26863196 MeRIP-seq:(Medium) rs11542299 Functional Loss SNV ICGC 33..33 33 LICA 1 - 116589 RMVar_ID_116589 Human_SNP_ID_810078669 m1A Human chr11 - 3129171 3129171 3129171 TGACCTCCTGCTGCCCCTCCTTCCTTCCTTCCAGAAGCCCCCGAGCGCCCACAGCATGAAGGAGG TGACCTCCTGCTGCCCCTCCTTCCTTCCTTCCGGAAGCCCCCGAGCGCCCACAGCATGAAGGAGG T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:3129101..3129245 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 3 lung 116590 RMVar_ID_116590 Human_SNP_ID_810084680 m1A Human chr11 - 68389919 68389919 68389919 GCCGCTCCTGCCCATCCAAGTTGGCACACTCGATTTTAGGGTTCTCTCCCCAGTCTGTCCAGTAC GCCGCTCCTGCCCATCCAAGTTGGCACACTCGGTTTTAGGGTTCTCTCCCCAGTCTGTCCAGTAC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68389901..68403682 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 116591 RMVar_ID_116591 Human_SNP_ID_810085287 m1A Human chr11 + 125626417 125626417 125626417 CGCTCCCTATATCCTCTTCCTCTCTTCCCCAGACCCCCACCTCTCCCTCCTCCTTCCCCAGTCGT CGCTCCCTATATCCTCTTCCTCTCTTCCCCAGCCCCCCACCTCTCCCTCCTCCTTCCCCAGTCGT A C CHEK1 Ensembl:ENSG00000149554 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:125626413..125626619 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas Human_RBP_ID_17791731 Human_Splice_Rec_1314344 RMVar_hsa_circ_126344,RMVar_hsa_circ_153893 116592 RMVar_ID_116592 Human_SNP_ID_810086068 m1A Human chr11 + 694992 694992 694992 CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCACCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT CGGCCGCCGCCGCCACAGCGGCCGCGGCCGCCGCCGCCGCCGCCTCAGCCAGGCCCAGCTGCTTT A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:694897..695009 26863410 MeRIP-seq:(Medium) rs767318857 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder 116593 RMVar_ID_116593 Human_SNP_ID_810088289 m1A Human chr11 - 72755078 72755078 72755078 GTACCCCGAGTGGAAACAGAAGCACCTGCCTCACTTCAAGCCGTGGCTGCACCCGGAGCAGAGCC GTACCCCGAGTGGAAACAGAAGCACCTGCCTCGCTTCAAGCCGTGGCTGCACCCGGAGCAGAGCC T C STARD10,ARAP1 Ensembl:ENSG00000214530,Ensembl:ENSG00000186635 Protein coding,Protein coding intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72754777..72755125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - Human_RBP_ID_9276046,Human_RBP_ID_22034819 Human_Splice_Rec_1275308,Human_Splice_Rec_1275322,Human_Splice_Rec_1275334,Human_Splice_Rec_1275346,Human_Splice_Rec_1275354,Human_Splice_Rec_1275358,Human_Splice_Rec_1275360,Human_Splice_Rec_1275372,Human_Splice_Rec_1275392,Human_Splice_Rec_1275398 RMVar_hsa_circ_123076,RMVar_hsa_circ_151561,RMVar_hsa_circ_151562,RMVar_hsa_circ_111149,RMVar_hsa_circ_122565,RMVar_hsa_circ_151563,RMVar_hsa_circ_151564 116594 RMVar_ID_116594 Human_SNP_ID_810091819 m1A Human chr11 - 125569527 125569527 125569527 CCGCGGCTCCGGCCCTGCCCCTAGCCCACCGCAGGCCAGCTCCGCCGGGGCGCTTCCAGGGCCGG CCGCGGCTCCGGCCCTGCCCCTAGCCCACCGCGGGCCAGCTCCGCCGGGGCGCTTCCAGGGCCGG T C FEZ1 Ensembl:ENSG00000149557 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:125569476..125569877 26863196 MeRIP-seq:(Medium) rs3017281 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 6 brain 116595 RMVar_ID_116595 Human_SNP_ID_810131533 m1A Human chr11 - 114400485 114400485 114400485 CTGCGCATGCTCGCCAGGATACCCCTCGTTAAAGGCAAGGCGGCTTCTGGCTCTTCCGCAGGCTC CTGCGCATGCTCGCCAGGATACCCCTCGTTAAGGGCAAGGCGGCTTCTGGCTCTTCCGCAGGCTC T C C11orf71 Ensembl:ENSG00000180425 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs606671 Functional Loss SNV ICGC 33..33 33 LUSC 1 - GWAS_ID_11568,GWAS_ID_11569,GWAS_ID_11570 116596 RMVar_ID_116596 Human_SNP_ID_810137706 m1A Human chr11 - 61132236 61132236 61132236 ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCATGGAGCCCTGCCACCGGCCCCTTTC ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCCCTGCCCATGGAGCCCTGCCACCGGCCCCTTTC T G VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61132185..61132433 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_4164594,Human_RBP_ID_5126573,Human_RBP_ID_5234993,Human_RBP_ID_17073686 Human_miRNA_ID_1293141,Human_miRNA_ID_1297166,Human_miRNA_ID_1417445,Human_miRNA_ID_2457432,Human_miRNA_ID_2462352,Human_miRNA_ID_2634995,Human_miRNA_ID_2637682 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 116597 RMVar_ID_116597 Human_SNP_ID_810137712 m1A Human chr11 - 61132236 61132236 61132236 ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCATGGAGCCCTGCCACCGGCCCCTTTC ACAGCCCATCCCCCAGCCTGCCTGTGGGCCCCGCTGCCCATGGAGCCCTGCCACCGGCCCCTTTC T C VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61132185..61132433 26863196 MeRIP-seq:(Medium) rs758133603 Functional Loss SNV COSMIC 33..33 33 lung non_small_cell_carcinoma 1 lung Human_RBP_ID_4164594,Human_RBP_ID_5126573,Human_RBP_ID_5234993,Human_RBP_ID_17073686 Human_miRNA_ID_1293141,Human_miRNA_ID_1297166,Human_miRNA_ID_1417445,Human_miRNA_ID_2457432,Human_miRNA_ID_2462352,Human_miRNA_ID_2634995,Human_miRNA_ID_2637682 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 116598 RMVar_ID_116598 Human_SNP_ID_810170587 m1A Human chr11 + 62678057 62678057 62678057 CCCTTGTCTCCTGCGCTGCCGTTCCCGTTCCAATGCCTCCCGTTCCTCTCTTTCTTCACGCTCCC CCCTTGTCTCCTGCGCTGCCGTTCCCGTTCCAGTGCCTCCCGTTCCTCTCTTTCTTCACGCTCCC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:62677891..62678093 26863196 MeRIP-seq:(Medium) rs371951393 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 116599 RMVar_ID_116599 Human_SNP_ID_810196744 m1A Human chr11 + 65307925 65307925 65307925 CTGGACCTCTCTTGTTTTCTGCTCATACCATGACTTTACTTGCAATCCTCCTGGCCTTTGCCTTG CTGGACCTCTCTTGTTTTCTGCTCATACCATGGCTTTACTTGCAATCCTCCTGGCCTTTGCCTTG A G AP000944.5 Ensembl:ENSG00000285816 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65307920..65308141 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_19657531,Human_RBP_ID_23513095 116600 RMVar_ID_116600 Human_SNP_ID_810197919 m1A Human chr11 - 114450029 114450027 114450029 TGCTCTGCCAAGCCATCAGCGTGAGAAAAAAAAACCACCAGAAGTTGCCTCCAGATAACGATGTA TGCTCTGCCAAGCCATCAGCGTGAGAAAAAAA__CCACCAGAAGTTGCCTCCAGATAACGATGTA GTT G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:114449978..114450079 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 STAD 1 - 116601 RMVar_ID_116601 Human_SNP_ID_810213568 m1A Human chr11 + 88312435 88312435 88312435 TTAAGGTGTGCTATGTTGACATACACATTCTCAGAGGCAGTTCCCACCTTCTTTCCGGTGAAACA TTAAGGTGTGCTATGTTGACATACACATTCTCGGAGGCAGTTCCCACCTTCTTTCCGGTGAAACA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:88312376..88312575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116602 RMVar_ID_116602 Human_SNP_ID_810216124 m1A Human chr11 - 66693073 66693073 66693073 CCCAGGATGAGCTGAGTGCCCAGGCAGAGGTGAAGAAGCACCAGGTGCTGGAGCAAGCCCTGGCC CCCAGGATGAGCTGAGTGCCCAGGCAGAGGTGGAGAAGCACCAGGTGCTGGAGCAAGCCCTGGCC T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:66693023..66693147;chr11:66693023..66693361 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 13 ovary Human_RBP_ID_871972,Human_RBP_ID_17805260 Human_Splice_Rec_1263822,Human_Splice_Rec_1263896,Human_Splice_Rec_1263968,Human_Splice_Rec_1264082 RMVar_hsa_circ_70940,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935 116603 RMVar_ID_116603 Human_SNP_ID_810231152 m1A Human chr11 + 65505836 65505835 65505837 TTAAACCAGTAAGTGGAGAAATAACATGTTCAAGAACTGTAATGCTGGGTGGGAACATGTAACTT TTAAACCAGTAAGTGGAGAAATAACATGTTCA__AACTGTAATGCTGGGTGGGAACATGTAACTT AAG A MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:65505786..65505956 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 LUAD 1 - Human_RBP_ID_1079333,Human_RBP_ID_1459286,Human_RBP_ID_1781506,Human_RBP_ID_2276176,Human_RBP_ID_3378123,Human_RBP_ID_5550000,Human_RBP_ID_6086272,Human_RBP_ID_8355924,Human_RBP_ID_9005482,Human_RBP_ID_9644989,Human_RBP_ID_10482325,Human_RBP_ID_11674076,Human_RBP_ID_17062325,Human_RBP_ID_17108752,Human_RBP_ID_17184765,Human_RBP_ID_17465779,Human_RBP_ID_17581387,Human_RBP_ID_17682414,Human_RBP_ID_18610991,Human_RBP_ID_19583102,Human_RBP_ID_21916498,Human_RBP_ID_22032870,Human_RBP_ID_22164926,Human_RBP_ID_22381306,Human_RBP_ID_22791801,Human_RBP_ID_22893154,Human_RBP_ID_23515190,Human_RBP_ID_24404325,Human_RBP_ID_24461909,Human_RBP_ID_24897203,Human_RBP_ID_26405953,Human_RBP_ID_26894605,Human_RBP_ID_27414390,Human_RBP_ID_27618994 Human_miRNA_ID_3175930,Human_miRNA_ID_3204430 RMVar_hsa_circ_150698,RMVar_hsa_circ_150699,RMVar_hsa_circ_150702 116604 RMVar_ID_116604 Human_SNP_ID_810237780 m1A Human chr11 - 35662970 35662970 35662970 CCCGCCTGGACCGCGCCGCGTCTCGAAGCGGGACCTGGGGCCGCGGCAGCCCCTGCCCGGGCGCA CCCGCCTGGACCGCGCCGCGTCTCGAAGCGGGCCCTGGGGCCGCGGCAGCCCCTGCCCGGGCGCA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:35662854..35663134 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 116605 RMVar_ID_116605 Human_SNP_ID_810264577 m1A Human chr11 + 18106009 18106009 18106009 CCGGCCACCTCCTCCTCCTCCTCCTTGTCGCGACCCGGCGGCGGCGGCGAGGGGTTGCGGTCCAT CCGGCCACCTCCTCCTCCTCCTCCTTGTCGCGGCCCGGCGGCGGCGGCGAGGGGTTGCGGTCCAT A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:18103276..18106075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 116606 RMVar_ID_116606 Human_SNP_ID_810272806 m1A Human chr11 + 640109 640109 640109 CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCAGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG CGACTGTGCGCCCGCCGCGCCCAGCCTCCCCCCGGACCCCTGCGGCCCCGACTGTGCGCCCCCCG A C DRD4 Ensembl:ENSG00000069696 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:639978..640162 26863196 MeRIP-seq:(Medium) rs769762387 Functional Loss SNV TCGA,COSMIC 33..33 33 MESO,lung adenocarcinoma,lung small_cell_carcinoma 3 lung 116607 RMVar_ID_116607 Human_SNP_ID_810276009 m1A Human chr11 + 64835533 64835533 64835533 TGTGGCTGTGGGCCTGCTCCAGCTGCTCTCGCAGGGCGGCCACCTCCTTCCTCAGTTGGGCCTCC TGTGGCTGTGGGCCTGCTCCAGCTGCTCTCGCGGGGCGGCCACCTCCTTCCTCAGTTGGGCCTCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64835501..64835602 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 116608 RMVar_ID_116608 Human_SNP_ID_810277721 m1A Human chr11 + 134382912 134382912 134382912 GCCGGTGGGGGTCAAACACCGTCTTCCAGCCGACCACCTTCCCTGCCCCGTTCACCCGTGGGGCC GCCGGTGGGGGTCAAACACCGTCTTCCAGCCGGCCACCTTCCCTGCCCCGTTCACCCGTGGGGCC A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:134382861..134382982 26863196 MeRIP-seq:(Medium) rs768927813 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus RMVar_hsa_circ_154135 116609 RMVar_ID_116609 Human_SNP_ID_810282660 m1A Human chr11 - 8914907 8914906 8914907 TACACTTACCTGACCATTCCCTATGTCCAAGCACATGTGCAGCTTCGACTCGCCTCTGTGATAAC TACACTTACCTGACCATTCCCTATGTCCAAGC_CATGTGCAGCTTCGACTCGCCTCTGTGATAAC GT G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:8914876..8914925 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 KIRC 1 - 116610 RMVar_ID_116610 Human_SNP_ID_810283163 m1A Human chr11 + 799293 799293 799293 CCCATCCACTGGGGAATATCTGGGCCAGCCTAAAAGTCTGTGGGGCCTAGGCCTGGGCAGGCTCT CCCATCCACTGGGGAATATCTGGGCCAGCCTACAAGTCTGTGGGGCCTAGGCCTGGGCAGGCTCT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:799242..799490 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus 116611 RMVar_ID_116611 Human_SNP_ID_810296406 m1A Human chr11 - 65333912 65333912 65333912 TAGGAGAGAAAGAAACGACCACTCACAGCTTCACTACATTCTCCACCACAGCCGCCATCTTCCCT TAGGAGAGAAAGAAACGACCACTCACAGCTTCGCTACATTCTCCACCACAGCCGCCATCTTCCCT T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65333903..65334021 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 116612 RMVar_ID_116612 Human_SNP_ID_810301562 m1A Human chr11 - 124660768 124660768 124660768 ACTCTGATACGTGGATGGTGGTACTGGATCCTATGAAGCCTGGAGGACCTTTCGAAGTGATGGCA ACTCTGATACGTGGATGGTGGTACTGGATCCTGTGAAGCCTGGAGGACCTTTCGAAGTGATGGCA T C SIAE Ensembl:ENSG00000110013 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs78778622 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1312342,Human_Splice_Rec_1312362,Human_Splice_Rec_1312384,Human_Splice_Rec_1312400,Human_Splice_Rec_1312406 Clinvar_Rec_467 GWAS_ID_10617,GWAS_ID_10618 RMVar_hsa_circ_33541 116613 RMVar_ID_116613 Human_SNP_ID_810318504 m1A Human chr11 + 65641097 65641097 65641097 CCCACTCCTGCGCAGCGGCAGCGATGCAGGCGAGGCCAGGCCCCCCACGCCAGCCAGCCCCCGTG CCCACTCCTGCGCAGCGGCAGCGATGCAGGCGGGGCCAGGCCCCCCACGCCAGCCAGCCCCCGTG A G SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65640971..65641137 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116614 RMVar_ID_116614 Human_SNP_ID_810330650 m1A Human chr11 - 379959 379959 379959 GCTCCACGTCCATATCCTCGCTCTCGAAATCCACCAGGACGACGCTGAAACGCGAGTCCCCGGTG GCTCCACGTCCATATCCTCGCTCTCGAAATCCGCCAGGACGACGCTGAAACGCGAGTCCCCGGTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:379910..380021 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116615 RMVar_ID_116615 Human_SNP_ID_810330971 m1A Human chr11 - 11964527 11964527 11964527 GAGCTGGAGGACCTGGAGAGGAGCCTGACTGAAGAGATGGCGCTGAGGGAGCCTGCGGCTGCCGC GAGCTGGAGGACCTGGAGAGGAGCCTGACTGAGGAGATGGCGCTGAGGGAGCCTGCGGCTGCCGC T C DKK3 Ensembl:ENSG00000050165 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:11964477..11964603 26863196 MeRIP-seq:(Medium) rs1442141496 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_148256,RMVar_hsa_circ_97794 116616 RMVar_ID_116616 Human_SNP_ID_810337380 m1A Human chr11 + 114447319 114447319 114447319 GAAATGAGGGGCTTGTATGATAAAAATGTGAGAGGGTCAGTTGACAGACACTCAGTGTTCGAATG GAAATGAGGGGCTTGTATGATAAAAATGTGAGGGGGTCAGTTGACAGACACTCAGTGTTCGAATG A G REXO2 Ensembl:ENSG00000076043 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:114447317..114447532 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11527554,Human_RBP_ID_23487290 RMVar_hsa_circ_153193,RMVar_hsa_circ_112275,RMVar_hsa_circ_153187,RMVar_hsa_circ_153189,RMVar_hsa_circ_375136,RMVar_hsa_circ_378725,RMVar_hsa_circ_122083,RMVar_hsa_circ_153190,RMVar_hsa_circ_153191,RMVar_hsa_circ_86783,RMVar_hsa_circ_153192 116617 RMVar_ID_116617 Human_SNP_ID_810340576 m1A Human chr11 - 118901423 118901423 118901423 CACCCATGGGGCCAGGCAACCTCAACATGAACATGAATGTCAACATGAACATGAACATGAACCTG CACCCATGGGGCCAGGCAACCTCAACATGAACGTGAATGTCAACATGAACATGAACATGAACCTG T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118901332..118901882 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney RMVar_hsa_circ_73107 116618 RMVar_ID_116618 Human_SNP_ID_810349608 m1A Human chr11 - 119018831 119018831 119018831 GCGTAGCTGTCCAACTGGTAAATCAAGCCGCCAGCTTTGTTCACCACATACACACTAAAAATCGC GCGTAGCTGTCCAACTGGTAAATCAAGCCGCCGGCTTTGTTCACCACATACACACTAAAAATCGC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119018751..119018975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116619 RMVar_ID_116619 Human_SNP_ID_810367687 m1A Human chr11 + 62611583 62611583 62611583 AGCCGCTGGCTCAGAGACTGGAGGGCCTCCCGAGCAGGGCCGTCACCTGGGAAAAGGGCAAGAGG AGCCGCTGGCTCAGAGACTGGAGGGCCTCCCGGGCAGGGCCGTCACCTGGGAAAAGGGCAAGAGG A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62611462..62611613 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine 116620 RMVar_ID_116620 Human_SNP_ID_810371163 m1A Human chr11 - 124118611 124118611 124118611 TCTCAATGCCATGCTGGGAATCTATGGTGGCGACCATGCTGAGTGTGTAGGGCAGGTCCTCCACA TCTCAATGCCATGCTGGGAATCTATGGTGGCGCCCATGCTGAGTGTGTAGGGCAGGTCCTCCACA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:124118560..124118651 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116621 RMVar_ID_116621 Human_SNP_ID_810397729 m1A Human chr11 - 118401657 118401657 118401657 AAGGTTACGGACAAATTGGGCCATGGTTCTGGAATGGAGAGTCCGTCGCCCCGAACCGCCGGCTG AAGGTTACGGACAAATTGGGCCATGGTTCTGGGATGGAGAGTCCGTCGCCCCGAACCGCCGGCTG T C AP001267.1 Ensembl:ENSG00000254873 lincRNA exon GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:118401601..118401823 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_Splice_Rec_1304067 116622 RMVar_ID_116622 Human_SNP_ID_810426540 m1A Human chr11 - 62841701 62841701 62841701 CCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCAC CCGAGGACAATATATTAAATGGATTTTTGGAACTAGGAGATGGAATAGGAGCTTGCTCCGTCCAC T G WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:62841651..62841814 26863196 MeRIP-seq:(Medium) rs77654912 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 116623 RMVar_ID_116623 Human_SNP_ID_810445899 m1A Human chr11 - 6601901 6601901 6601901 GAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCCCCTATAAATTCAGCCCAGCACCTGGA GAAGATGAGAAAAGAAAGAGGAAATGCCAGAACCATGCCCCTATAAATTCAGCCCAGCACCTGGA T G RRP8 Ensembl:ENSG00000132275 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:6601843..6601935 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_3940187,Human_RBP_ID_5344866,Human_RBP_ID_26319564,Human_RBP_ID_26804398,Human_RBP_ID_27803221 Human_Splice_Rec_1204913,Human_Splice_Rec_1204935,Human_Splice_Rec_1204943 RMVar_hsa_circ_13756,RMVar_hsa_circ_112068,RMVar_hsa_circ_147868,RMVar_hsa_circ_346369,RMVar_hsa_circ_42283 116624 RMVar_ID_116624 Human_SNP_ID_810484976 m1A Human chr11 + 3206837 3206837 3206837 TGATGGTGATGATGGTGATGATGATAATGGTGATGATGGTGATAATGGTGATGATGGTAATGGTG TGATGGTGATGATGGTGATGATGATAATGGTGGTGATGGTGATAATGGTGATGATGGTAATGGTG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3206750..3206884 26863196 MeRIP-seq:(Medium) rs750715477 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116625 RMVar_ID_116625 Human_SNP_ID_810485999 m1A Human chr11 + 76797355 76797355 76797355 GGACCCAATGCACTTTCTTGTCTCCTCTAATAAGCCCCACCCTCCCCGCCTGGGCTCCCCTTGCT GGACCCAATGCACTTTCTTGTCTCCTCTAATAGGCCCCACCCTCCCCGCCTGGGCTCCCCTTGCT A G TSKU Ensembl:ENSG00000182704 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:76797307..76797408 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_404053,Human_RBP_ID_2285264,Human_RBP_ID_18933898,Human_RBP_ID_27416356 Human_miRNA_ID_2146747,Human_miRNA_ID_2988172,Human_miRNA_ID_3021872 RMVar_hsa_circ_100357,RMVar_hsa_circ_151860 116626 RMVar_ID_116626 Human_SNP_ID_810518767 m1A Human chr11 + 66287666 66287666 66287666 GGGGGGGCAGAGGAGCATCACGACTGTACTGCACTTCCCAGTTCTGGCAGTGGCAGTGGCAGCAG GGGGGGGCAGAGGAGCATCACGACTGTACTGCGCTTCCCAGTTCTGGCAGTGGCAGTGGCAGCAG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:66287615..66287965 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 116627 RMVar_ID_116627 Human_SNP_ID_810520966 m1A Human chr11 + 62617034 62617034 62617034 CCGGCTGTAGGTGTTGTCATCGTCAGCAAAGTAGACGACTCCTTGGGTCCCTGGTGGTGGTGGGT CCGGCTGTAGGTGTTGTCATCGTCAGCAAAGTGGACGACTCCTTGGGTCCCTGGTGGTGGTGGGT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62616941..62617079 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 116628 RMVar_ID_116628 Human_SNP_ID_810521425 m1A Human chr11 - 65501632 65501632 65501632 TGAAGGTGTTCGTGCCAACAGCACAGCGGTACACTCCTTCTCTAACCCAGTTTGTCAATAGTACT TGAAGGTGTTCGTGCCAACAGCACAGCGGTACGCTCCTTCTCTAACCCAGTTTGTCAATAGTACT T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4,TALAM1-001:5 RNACentral:URS00008B3291,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF,RNACentral:URS00008BCC03 lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA,lincRNA exon,intron,exon,intron,intron,intron,exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65501518..65501787 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 116629 RMVar_ID_116629 Human_SNP_ID_810522705 m1A Human chr11 - 61873745 61873745 61873745 ACCAGCAACCAAGCCAGCCCCCGGCGGGATCGATACCCTCACCCCTCCACTGGCCAGCCTGGGGG ACCAGCAACCAAGCCAGCCCCCGGCGGGATCGGTACCCTCACCCCTCCACTGGCCAGCCTGGGGG T C FADS3 Ensembl:ENSG00000221968 Protein coding 3'UTR GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_17649598 RMVar_hsa_circ_104890,RMVar_hsa_circ_126843,RMVar_hsa_circ_119181,RMVar_hsa_circ_119309,RMVar_hsa_circ_118092,RMVar_hsa_circ_150113,RMVar_hsa_circ_84299,RMVar_hsa_circ_96611,RMVar_hsa_circ_150115,RMVar_hsa_circ_150117,RMVar_hsa_circ_80076,RMVar_hsa_circ_150116,RMVar_hsa_circ_150114,RMVar_hsa_circ_150111,RMVar_hsa_circ_150112,RMVar_hsa_circ_150110 116630 RMVar_ID_116630 Human_SNP_ID_810548129 m1A Human chr11 + 63681644 63681644 63681644 TTCTCCCACCCTCGCTCGCGTAGCCATGGCGGAGCCGTCGGCGGCCACTCAGTCCCATTCCATCT TTCTCCCACCCTCGCTCGCGTAGCCATGGCGGGGCCGTCGGCGGCCACTCAGTCCCATTCCATCT A G RTN3 Ensembl:ENSG00000133318 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:63681557..63681712 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_227621,Human_RBP_ID_399477,Human_RBP_ID_752131,Human_RBP_ID_987761,Human_RBP_ID_4168024,Human_RBP_ID_9321487,Human_RBP_ID_11662140,Human_RBP_ID_17350199,Human_RBP_ID_18933586,Human_RBP_ID_22433047,Human_RBP_ID_22532359 116631 RMVar_ID_116631 Human_SNP_ID_810550248 m1A Human chr11 + 709401 709401 709401 AGGTCTGCCCTTCTCCCGCTGGCCGCCACCCAAGACACCATGAGCCAGTCCGGGGCCGTGAGCTG AGGTCTGCCCTTCTCCCGCTGGCCGCCACCCAGGACACCATGAGCCAGTCCGGGGCCGTGAGCTG A G EPS8L2 Ensembl:ENSG00000177106 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:709321..709426 26863196 MeRIP-seq:(Medium) rs10902202 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_867010,Human_RBP_ID_18971570 Human_Splice_Rec_1194436,Human_Splice_Rec_1194437,Human_Splice_Rec_1194446,Human_Splice_Rec_1194447,Human_Splice_Rec_1194452,Human_Splice_Rec_1194453,Human_Splice_Rec_1194492,Human_Splice_Rec_1194493,Human_Splice_Rec_1194534,Human_Splice_Rec_1194535,Human_Splice_Rec_1194542,Human_Splice_Rec_1194543,Human_Splice_Rec_1194560,Human_Splice_Rec_1194561,Human_Splice_Rec_1194600,Human_Splice_Rec_1194601,Human_Splice_Rec_1194640,Human_Splice_Rec_1194641,Human_Splice_Rec_1194644,Human_Splice_Rec_1194645,Human_Splice_Rec_1194650,Human_Splice_Rec_1194651,Human_Splice_Rec_1194692,Human_Splice_Rec_1194693,Human_Splice_Rec_1194700,Human_Splice_Rec_1194701,Human_Splice_Rec_1194708,Human_Splice_Rec_1194709,Human_Splice_Rec_1194716,Human_Splice_Rec_1194717,Human_Splice_Rec_1194720,Human_Splice_Rec_1194721,Human_Splice_Rec_1194759 Human_miRNA_ID_2083410 RMVar_hsa_circ_88989,RMVar_hsa_circ_147442 116632 RMVar_ID_116632 Human_SNP_ID_810564592 m1A Human chr11 - 6390529 6390529 6390529 GTCCCCCCCGGCCTGGACCCTAGCCAGCCCTCAGGGCCCCGGGCGGCGCCGGGGACACCCGATTA GTCCCCCCCGGCCTGGACCCTAGCCAGCCCTCTGGGCCCCGGGCGGCGCCGGGGACACCCGATTA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6390444..6390650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 116633 RMVar_ID_116633 Human_SNP_ID_810583166 m1A Human chr11 - 66705356 66705356 66705356 GCAGCGGCGCGGCGGGCCCGGCTGGAGGAATCACGGCGGCTCTGGCGTTTCCTCTGGGAGGTGGG GCAGCGGCGCGGCGGGCCCGGCTGGAGGAATCGCGGCGGCTCTGGCGTTTCCTCTGGGAGGTGGG T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66705111..66705466 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_8771331,Human_RBP_ID_27415077 Human_miRNA_ID_3010639 RMVar_hsa_circ_89055,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_122362,RMVar_hsa_circ_150936,RMVar_hsa_circ_150938,RMVar_hsa_circ_79569,RMVar_hsa_circ_150939,RMVar_hsa_circ_150937 116634 RMVar_ID_116634 Human_SNP_ID_810591356 m1A Human chr11 - 6611981 6611981 6611981 GGGCACGGGACCCTTGGCGGCGCGGGCCGGGGAGCCAGCTGAGCGGCGTGGGGCGGGTGAGGGCC GGGCACGGGACCCTTGGCGGCGCGGGCCGGGGTGCCAGCTGAGCGGCGTGGGGCGGGTGAGGGCC T A AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding intron,CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:6611701..6612200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_226111,Human_RBP_ID_401575,Human_RBP_ID_806796,Human_RBP_ID_868624,Human_RBP_ID_4183940,Human_RBP_ID_5086761,Human_RBP_ID_5110350,Human_RBP_ID_5644343,Human_RBP_ID_8174135,Human_RBP_ID_9321296,Human_RBP_ID_9414835 Human_Splice_Rec_1205185,Human_Splice_Rec_1205207 RMVar_hsa_circ_99612,RMVar_hsa_circ_147882 116635 RMVar_ID_116635 Human_SNP_ID_810613503 m1A Human chr11 - 66617217 66617214 66617217 CTTGGTGGACGGTTCCTGGACCGCAGGGGAGGAGGGTGGCTCTACCCAACGCGCCCCCAACACCT CTTGGTGGACGGTTCCTGGACCGCAGGGGAGG___GTGGCTCTACCCAACGCGCCCCCAACACCT CCCT C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:66617166..66617279 26863196 MeRIP-seq:(Medium) rs949083846 Functional Loss DEL ICGC 33..35 33 ESCA 1 - 116636 RMVar_ID_116636 Human_SNP_ID_810641467 m1A Human chr11 - 118907561 118907561 118907561 CGCGGAGTAAGCGGCGCTGTGTGCTGGAGCGGAAGCAGCCGTACAGTGGGGACGAATGGTGCTCT CGCGGAGTAAGCGGCGCTGTGTGCTGGAGCGGGAGCAGCCGTACAGTGGGGACGAATGGTGCTCT T C BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118907461..118907615 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_866194,Human_RBP_ID_5344466,Human_RBP_ID_9362992,Human_RBP_ID_18972807,Human_RBP_ID_22895773 Human_Splice_Rec_1305654,Human_Splice_Rec_1305655,Human_Splice_Rec_1305668,Human_Splice_Rec_1305669,Human_Splice_Rec_1305682,Human_Splice_Rec_1305683 RMVar_hsa_circ_72117 116637 RMVar_ID_116637 Human_SNP_ID_810646425 m1A Human chr11 - 65333907 65333907 65333907 GAGAAAGAAACGACCACTCACAGCTTCACTACATTCTCCACCACAGCCGCCATCTTCCCTGTTCC GAGAAAGAAACGACCACTCACAGCTTCACTACGTTCTCCACCACAGCCGCCATCTTCCCTGTTCC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65333901..65334011 26863196 MeRIP-seq:(Medium) rs146359123 Functional Loss SNV ICGC 33..33 33 COCA 1 - 116638 RMVar_ID_116638 Human_SNP_ID_810686808 m1A Human chr11 - 1558152 1558152 1558152 ATGCGGGTCCCCATCAACGACAACTACTGTGAAAAACTGCTGCCCTGGCTGGACAAGTCCATCGA ATGCGGGTCCCCATCAACGACAACTACTGTGAGAAACTGCTGCCCTGGCTGGACAAGTCCATCGA T C DUSP8 Ensembl:ENSG00000184545 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1558088..1558155 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_1197765,Human_Splice_Rec_1197777,Human_Splice_Rec_1197785 RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 116639 RMVar_ID_116639 Human_SNP_ID_810704819 m1A Human chr11 + 18634368 18634368 18634368 GCCAACTGCACTGCCTCGGGAGCCCCACTCCCACCCCGCCTCTGCGGGACCACTTCCGGCGCCTT GCCAACTGCACTGCCTCGGGAGCCCCACTCCCCCCCCGCCTCTGCGGGACCACTTCCGGCGCCTT A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:18634318..18634460 26863196 MeRIP-seq:(Medium) rs975977724 Functional Loss SNV COSMIC 33..33 33 meninges meningothelial 1 brain 116640 RMVar_ID_116640 Human_SNP_ID_810715883 m1A Human chr11 - 28097973 28097973 28097973 TTTTAATTTCAGAGAAGTATTCAAGTATTTATACAGATAGGAATCAAGATAATCAACAATGTCTG TTTTAATTTCAGAGAAGTATTCAAGTATTTATGCAGATAGGAATCAAGATAATCAACAATGTCTG T C KIF18A Ensembl:ENSG00000121621 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:28097923..28098015 26863196 MeRIP-seq:(Medium) rs1181493456 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22034337,Human_RBP_ID_23500132,Human_RBP_ID_27803313 Human_Splice_Rec_1222766,Human_Splice_Rec_1222818 RMVar_hsa_circ_8134,RMVar_hsa_circ_86626,RMVar_hsa_circ_32143,RMVar_hsa_circ_148800,RMVar_hsa_circ_148804,RMVar_hsa_circ_106119,RMVar_hsa_circ_66920 116641 RMVar_ID_116641 Human_SNP_ID_810726848 m1A Human chr11 - 119373300 119373300 119373300 GTTTCAAGCCGGTCCCCACCAGCAGCTTCCTCACCCGTCCCCGTACCTATGGCCCCTCCTCCCTC GTTTCAAGCCGGTCCCCACCAGCAGCTTCCTCGCCCGTCCCCGTACCTATGGCCCCTCCTCCCTC T C USP2 Ensembl:ENSG00000036672 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119373249..119373362 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach RMVar_hsa_circ_95829,RMVar_hsa_circ_153557 116642 RMVar_ID_116642 Human_SNP_ID_810751541 m1A Human chr11 + 65642348 65642348 65642348 AGAAGGAGGGCAGCGGAGGGGGCACCCTGCACAGCTACCGCGTCATCGTGCGGACCACGCAGGTG AGAAGGAGGGCAGCGGAGGGGGCACCCTGCACGGCTACCGCGTCATCGTGCGGACCACGCAGGTG A G SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65642298..65642646 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_866674,Human_RBP_ID_3939451 Human_Splice_Rec_1259650,Human_Splice_Rec_1259651,Human_Splice_Rec_1259686,Human_Splice_Rec_1259687,Human_Splice_Rec_1259718,Human_Splice_Rec_1259719,Human_Splice_Rec_1259745 116643 RMVar_ID_116643 Human_SNP_ID_810751628 m1A Human chr11 + 68938279 68938279 68938279 GCTGATAACACCTGCGGCTTTGCCAAGTGCACAGCCGGCGTCACAACCCTGGGCCAGTTCTGCCA GCTGATAACACCTGCGGCTTTGCCAAGTGCACCGCCGGCGTCACAACCCTGGGCCAGTTCTGCCA A C IGHMBP2 Ensembl:ENSG00000132740 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:68938229..68939558 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_Splice_Rec_1269510,Human_Splice_Rec_1269511,Human_Splice_Rec_1269550,Human_Splice_Rec_1269551,Human_Splice_Rec_1269563 RMVar_hsa_circ_96647,RMVar_hsa_circ_151328 116644 RMVar_ID_116644 Human_SNP_ID_810754033 m1A Human chr11 + 65613448 65613448 65613448 AAGCTGGCCACCTCGCAGGGGGGCGGGCCGCCACCCCGAGACACATAGTTGGACGGGAAGATGCC AAGCTGGCCACCTCGCAGGGGGGCGGGCCGCCGCCCCGAGACACATAGTTGGACGGGAAGATGCC A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65613404..65613531 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116645 RMVar_ID_116645 Human_SNP_ID_810758771 m1A Human chr11 + 65966511 65966511 65966511 AAGCTGCGGCTGCAGGCTCAGTCCCTGAGCACAGTGGGGCCCCGGCTGGCCTCCGAATACCTCAC AAGCTGCGGCTGCAGGCTCAGTCCCTGAGCACGGTGGGGCCCCGGCTGGCCTCCGAATACCTCAC A G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65966330..65966581 26863196 MeRIP-seq:(Medium) rs1286589424 Functional Loss SNV TCGA 33..33 33 LGG 1 - Human_RBP_ID_31621,Human_RBP_ID_8773741,Human_RBP_ID_9275904 Human_Splice_Rec_1261259,Human_Splice_Rec_1261289 Human_miRNA_ID_2295599,Human_miRNA_ID_2397745 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184,RMVar_hsa_circ_336615 116646 RMVar_ID_116646 Human_SNP_ID_810762554 m1A Human chr11 + 60936914 60936914 60936914 TGGAGAGGATCCGGGGCAGCTCCTGACCCTCCACAGCCACCTGGTCAGCCACCAGCTGGGGCAAC TGGAGAGGATCCGGGGCAGCTCCTGACCCTCCGCAGCCACCTGGTCAGCCACCAGCTGGGGCAAC A G TMEM132A Ensembl:ENSG00000006118 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:60936864..60937041 26863196 MeRIP-seq:(Medium) rs1292965483 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_398233,Human_RBP_ID_748845,Human_RBP_ID_5111082,Human_RBP_ID_17805882 RMVar_hsa_circ_91410,RMVar_hsa_circ_149896 116647 RMVar_ID_116647 Human_SNP_ID_810765163 m1A Human chr11 - 62575659 62575659 62575659 GCAGCAGGGATGTGCAGGGGACGGTGGGGAAGACAGGGTAGAAGAGATGGTTATAGAGGTTGGAG GCAGCAGGGATGTGCAGGGGACGGTGGGGAAGCCAGGGTAGAAGAGATGGTTATAGAGGTTGGAG T G AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding intron,CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62575518..62575828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_259722,Human_RBP_ID_8246411,Human_RBP_ID_18159691,Human_RBP_ID_18510668,Human_RBP_ID_18526351,Human_RBP_ID_18932443,Human_RBP_ID_21916926 116648 RMVar_ID_116648 Human_SNP_ID_810768496 m1A Human chr11 - 72018832 72018832 72018832 AGCTGGAGCTAGCTGAGAACCGCAAGCTCCTCACCGAGAAGGGTAGGTGGCTGGCACACTGGCAG AGCTGGAGCTAGCTGAGAACCGCAAGCTCCTCGCCGAGAAGGGTAGGTGGCTGGCACACTGGCAG T C NUMA1 Ensembl:ENSG00000137497 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72017625..72018947 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,HNSC,head_neck squamous_cell_carcinoma,brain astrocytoma_Grade_IV 14 head and neck,brain Human_RBP_ID_871496,Human_RBP_ID_3941051,Human_RBP_ID_5520846,Human_RBP_ID_17805300,Human_RBP_ID_18974615,Human_RBP_ID_22893783,Human_RBP_ID_23113132 Human_Splice_Rec_1272249,Human_Splice_Rec_1272299,Human_Splice_Rec_1272349,Human_Splice_Rec_1272397,Human_Splice_Rec_1272447,Human_Splice_Rec_1272491,Human_Splice_Rec_1272561,Human_Splice_Rec_1272589,Human_Splice_Rec_1272617,Human_Splice_Rec_1272641,Human_Splice_Rec_1272663 RMVar_hsa_circ_7616,RMVar_hsa_circ_103869,RMVar_hsa_circ_151494,RMVar_hsa_circ_113356,RMVar_hsa_circ_96395,RMVar_hsa_circ_151495,RMVar_hsa_circ_151496,RMVar_hsa_circ_48545,RMVar_hsa_circ_42905 116649 RMVar_ID_116649 Human_SNP_ID_810801973 m1A Human chr11 - 72103233 72103233 72103233 CCCTCCTCGGCGCGGCCTGAGCGCCCGGCCCGACCCCGGCCATGGGGTGCTGCTACAGCAGCGAG CCCTCCTCGGCGCGGCCTGAGCGCCCGGCCCGGCCCCGGCCATGGGGTGCTGCTACAGCAGCGAG T C LAMTOR1 Ensembl:ENSG00000149357 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr11:72103152..72103331;chr11:72103106..72103275;chr11:72103085..72103300;chr11:72103120..72103265;chr11:72100681..72103238 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_226697,Human_RBP_ID_403056,Human_RBP_ID_4177401,Human_RBP_ID_9321704,Human_RBP_ID_18416622 Human_Splice_Rec_1273119,Human_Splice_Rec_1273127,Human_Splice_Rec_1273137,Human_Splice_Rec_1273145,Human_Splice_Rec_1273151,Human_Splice_Rec_1273167 RMVar_hsa_circ_112115,RMVar_hsa_circ_151502 116650 RMVar_ID_116650 Human_SNP_ID_810802664 m1A Human chr11 - 709680 709680 709680 GGCCAGACCAGGCACAGCTGTGGGGCAGGAGCAGCTGTCCCCCACCTGGATGCAGTGCCCATTTC GGCCAGACCAGGCACAGCTGTGGGGCAGGAGCGGCTGTCCCCCACCTGGATGCAGTGCCCATTTC T C AP006621.4 Ensembl:ENSG00000269915 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:709529..709715 26863196 MeRIP-seq:(Medium) rs11605783 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,liver hepatocellular_carcinoma 9 liver 116651 RMVar_ID_116651 Human_SNP_ID_810809397 m1A Human chr11 - 119048826 119048825 119048827 CTGAGGGCGTCGCTCCAGCCCCAGAGGGAGAGAAGAAGCAGAAGCCCGCCAGGAAGCGGCGAATG CTGAGGGCGTCGCTCCAGCCCCAGAGGGAGA__AGAAGCAGAAGCCCGCCAGGAAGCGGCGAATG TTC T HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:119048776..119048909 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 32..33 33 SKCM 2 - Human_RBP_ID_226707,Human_RBP_ID_807410,Human_RBP_ID_871558,Human_RBP_ID_3939886,Human_RBP_ID_9276115,Human_RBP_ID_9322359,Human_RBP_ID_9363017,Human_RBP_ID_18469103,Human_RBP_ID_19697663,Human_RBP_ID_22755062,Human_RBP_ID_26317868,Human_RBP_ID_27805145 Human_Splice_Rec_1306264,Human_Splice_Rec_1306358,Human_Splice_Rec_1306408,Human_Splice_Rec_1306494,Human_Splice_Rec_1306546 Human_miRNA_ID_3117815 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 116652 RMVar_ID_116652 Human_SNP_ID_810810933 m1A Human chr11 - 234102 234102 234102 TTTCAGTGACTCACAAACATTTTATTTACGTAAATGAGGAATGTACTCAGGCACCCTTCGTGATA TTTCAGTGACTCACAAACATTTTATTTACGTAGATGAGGAATGTACTCAGGCACCCTTCGTGATA T C SIRT3 Ensembl:ENSG00000142082 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10794302 Functional Loss SNV ICGC 33..33 33 ESCA 2 - GWAS_ID_6732,GWAS_ID_6733,GWAS_ID_6734,GWAS_ID_6735,GWAS_ID_6736,GWAS_ID_6737,GWAS_ID_6738,GWAS_ID_6739,GWAS_ID_6740,GWAS_ID_6741,GWAS_ID_6742,GWAS_ID_6743,GWAS_ID_6744,GWAS_ID_6745,GWAS_ID_6746,GWAS_ID_6747,GWAS_ID_6748,GWAS_ID_6749,GWAS_ID_6750,GWAS_ID_6751,GWAS_ID_6752,GWAS_ID_6753,GWAS_ID_6754,GWAS_ID_6755,GWAS_ID_6756,GWAS_ID_6757,GWAS_ID_6758,GWAS_ID_6759,GWAS_ID_6760,GWAS_ID_6761,GWAS_ID_6762,GWAS_ID_6763,GWAS_ID_6764,GWAS_ID_6765,GWAS_ID_6766,GWAS_ID_6767,GWAS_ID_6768,GWAS_ID_6769,GWAS_ID_6770,GWAS_ID_6771,GWAS_ID_6772,GWAS_ID_6773,GWAS_ID_6774,GWAS_ID_6775,GWAS_ID_6776,GWAS_ID_6777,GWAS_ID_6778,GWAS_ID_6779,GWAS_ID_6780,GWAS_ID_6781,GWAS_ID_6782,GWAS_ID_6783,GWAS_ID_6784,GWAS_ID_6785,GWAS_ID_6786,GWAS_ID_6787,GWAS_ID_6788,GWAS_ID_6789,GWAS_ID_6790,GWAS_ID_6791,GWAS_ID_6792,GWAS_ID_6793,GWAS_ID_6794,GWAS_ID_6795,GWAS_ID_6796 RMVar_hsa_circ_147357,RMVar_hsa_circ_75729 116653 RMVar_ID_116653 Human_SNP_ID_810819592 m1A Human chr11 + 102229751 102229751 102229751 AGCACCCTGCCCTCACAGCAGAACCGTTTCCCAGACTACCTTGAAGCCATTCCTGGGACAAATGT AGCACCCTGCCCTCACAGCAGAACCGTTTCCCGGACTACCTTGAAGCCATTCCTGGGACAAATGT A G YAP1 Ensembl:ENSG00000137693 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:102229680..102229773 26863196 MeRIP-seq:(Medium) rs201530575 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_17235315 Human_Splice_Rec_1291232,Human_Splice_Rec_1291244,Human_Splice_Rec_1291258,Human_Splice_Rec_1291274,Human_Splice_Rec_1291288,Human_Splice_Rec_1291300,Human_Splice_Rec_1291314,Human_Splice_Rec_1291330,Human_Splice_Rec_1291342,Human_Splice_Rec_1291346 Human_miRNA_ID_2043244,Human_miRNA_ID_2045394,Human_miRNA_ID_2168427,Human_miRNA_ID_2169950 116654 RMVar_ID_116654 Human_SNP_ID_810840849 m1A Human chr11 + 47639031 47639031 47639031 TGCCGCCCAAAAATATTTCGTCCTATTGTTGGAGGAAGAGGCTCATATCCCACCTTTAAAAACAA TGCCGCCCAAAAATATTTCGTCCTATTGTTGGGGGAAGAGGCTCATATCCCACCTTTAAAAACAA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47638980..47642550 26863196 MeRIP-seq:(Medium) rs1355103595 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 116655 RMVar_ID_116655 Human_SNP_ID_810842259 m1A Human chr11 - 118481994 118481987 118481994 TTGGCGGTCCTGTAGTAGGTGGCTGAGGCGGGATGACCAGTGCTGGCTGGGAGACCTGCTTGCTT TTGGCGGTCCTGTAGTAGGTGGCTGAGGCGGG_______GTGCTGGCTGGGAGACCTGCTTGCTT CTGGTCAT C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:118481943..118482078 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..39 33 SARC 1 - 116656 RMVar_ID_116656 Human_SNP_ID_810862612 m1A Human chr11 - 623510 623510 623510 AGAGAAATCCCAACCACCCTATGCCCTGTTGCATCCCAGCCCCGCTCCCCCAACATCCTGCTTCT AGAGAAATCCCAACCACCCTATGCCCTGTTGCTTCCCAGCCCCGCTCCCCCAACATCCTGCTTCT T A CDHR5 Ensembl:ENSG00000099834 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:623503..624223 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_6082370 116657 RMVar_ID_116657 Human_SNP_ID_810879371 m1A Human chr11 - 117315561 117315561 117315561 GGGGCAAGTCGGGGCAGGGCTACTACGTGGAGATGACCGTGGGCAGCCCCCCGCAGACGGTAAGG GGGGCAAGTCGGGGCAGGGCTACTACGTGGAGGTGACCGTGGGCAGCCCCCCGCAGACGGTAAGG T C BACE1 Ensembl:ENSG00000186318 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:117315559..117315660 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 7 stomach Human_Splice_Rec_1302039,Human_Splice_Rec_1302069,Human_Splice_Rec_1302097,Human_Splice_Rec_1302113,Human_Splice_Rec_1302129,Human_Splice_Rec_1302173 116658 RMVar_ID_116658 Human_SNP_ID_810879906 m1A Human chr11 + 64790253 64790253 64790253 CAGGTGCCAGTGTGGCCGTGGGCTCGCCCTGCATGTTGACAATCCTCACACAGCCTGCACAGGGA CAGGTGCCAGTGTGGCCGTGGGCTCGCCCTGCGTGTTGACAATCCTCACACAGCCTGCACAGGGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64789612..64792314 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_104351,RMVar_hsa_circ_150500 116659 RMVar_ID_116659 Human_SNP_ID_810896268 m1A Human chr11 + 95904945 95904945 95904945 AAATCCACTTCAGTCAGGCCTTTGCCTCCACCACACCAACAAAAATGCTTTTGTCAAGGTCATCA AAATCCACTTCAGTCAGGCCTTTGCCTCCACCGCACCAACAAAAATGCTTTTGTCAAGGTCATCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:95904942..95905247 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 116660 RMVar_ID_116660 Human_SNP_ID_810899640 m1A Human chr11 + 67282795 67282795 67282795 TCCGGCAGCACAAGACCAAAGACAAGCATGAGATCGACCGCATGACGCTGACGATGGTGGGTGCA TCCGGCAGCACAAGACCAAAGACAAGCATGAGTTCGACCGCATGACGCTGACGATGGTGGGTGCA A T GRK2 Ensembl:ENSG00000173020 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67282792..67283201 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22491689 Human_Splice_Rec_1265394,Human_Splice_Rec_1265395,Human_Splice_Rec_1265458,Human_Splice_Rec_1265459,Human_Splice_Rec_1265486,Human_Splice_Rec_1265487,Human_Splice_Rec_1265502,Human_Splice_Rec_1265503,Human_Splice_Rec_1265514,Human_Splice_Rec_1265515,Human_Splice_Rec_1265524,Human_Splice_Rec_1265525,Human_Splice_Rec_1265536,Human_Splice_Rec_1265537,Human_Splice_Rec_1265539 RMVar_hsa_circ_6765,RMVar_hsa_circ_127619,RMVar_hsa_circ_151036,RMVar_hsa_circ_31911,RMVar_hsa_circ_13279,RMVar_hsa_circ_356572,RMVar_hsa_circ_4602,RMVar_hsa_circ_359863,RMVar_hsa_circ_53577,RMVar_hsa_circ_15031,RMVar_hsa_circ_151039,RMVar_hsa_circ_371384 116661 RMVar_ID_116661 Human_SNP_ID_810937420 m1A Human chr11 - 75404763 75404763 75404763 GTGGTGGGCAGTATCTCATCTTTGGGTTCCACAATGCTCACGTGGTCAGGCAGGGGCTTCTTAGG GTGGTGGGCAGTATCTCATCTTTGGGTTCCACGATGCTCACGTGGTCAGGCAGGGGCTTCTTAGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:75404651..75404875;chr11:75403932..75404850 32194978 MeRIP-seq:(Medium) rs1278748349 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma,endometrium mixed_endometrioid_and_clear_cell_carcinoma 12 uterus,large intestine 116662 RMVar_ID_116662 Human_SNP_ID_810939735 m1A Human chr11 - 65887683 65887683 65887683 TTGATGAGGCCTTTGTTCGGGAGGTGCTGGGCAAGAAGCTGTCCAAAGGCACCAAGAAAGACCTG TTGATGAGGCCTTTGTTCGGGAGGTGCTGGGCGAGAAGCTGTCCAAAGGCACCAAGAAAGACCTG T C FIBP Ensembl:ENSG00000172500 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65887598..65887796 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_401114,Human_RBP_ID_4172905,Human_RBP_ID_18611173 Human_Splice_Rec_1260972,Human_Splice_Rec_1260973,Human_Splice_Rec_1260998,Human_Splice_Rec_1260999,Human_Splice_Rec_1261034,Human_Splice_Rec_1261035,Human_Splice_Rec_1261052,Human_Splice_Rec_1261053,Human_Splice_Rec_1261072,Human_Splice_Rec_1261073,Human_Splice_Rec_1261082,Human_Splice_Rec_1261083,Human_Splice_Rec_1261090,Human_Splice_Rec_1261091,Human_Splice_Rec_1261098 RMVar_hsa_circ_24457,RMVar_hsa_circ_372939,RMVar_hsa_circ_37614,RMVar_hsa_circ_150808 116663 RMVar_ID_116663 Human_SNP_ID_810940278 m1A Human chr11 - 120429480 120429480 120429480 GCCGTTCCTGTTCTTTCTGTAACATTTTTCTCAGAATTTCTACTTTCTGGTTATGAACCACATTG GCCGTTCCTGTTCTTTCTGTAACATTTTTCTCGGAATTTCTACTTTCTGGTTATGAACCACATTG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:120428137..120429480 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck 116664 RMVar_ID_116664 Human_SNP_ID_810951002 m1A Human chr11 - 8730088 8730088 8730088 CAAGCGCACCTTTGAATACGAGGCTGACAAGAACCCCAAGAGTAAGCCCAGTAATGGTCTACCTC CAAGCGCACCTTTGAATACGAGGCTGACAAGACCCCCAAGAGTAAGCCCAGTAATGGTCTACCTC T G DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:8729985..8730200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_miRNA_ID_2553985 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_81067,RMVar_hsa_circ_80502,RMVar_hsa_circ_147962,RMVar_hsa_circ_75978,RMVar_hsa_circ_147965,RMVar_hsa_circ_124340,RMVar_hsa_circ_147966,RMVar_hsa_circ_314841,RMVar_hsa_circ_147967,RMVar_hsa_circ_341464,RMVar_hsa_circ_14271,RMVar_hsa_circ_147968 116665 RMVar_ID_116665 Human_SNP_ID_810954632 m1A Human chr11 - 72751330 72751330 72751330 CAATTTACAAGGATAAGGACCCTCCAAAGGCGAGGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA CAATTTACAAGGATAAGGACCCTCCAAAGGCGGGGGCGTAGCTTGTGCAAAGTCAGGAATTTGGA T C ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:72751317..72751414 26863196 MeRIP-seq:(Medium) rs1785212 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_151561 116666 RMVar_ID_116666 Human_SNP_ID_810961250 m1A Human chr11 - 802379 802379 802379 TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCAAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC TCCTTCCTCACTCAGCTTTCCTGTGACCCCTCGAGGCTGCTCAGTGACCCTGGCCTGTGGCGTCC T C PIDD1 Ensembl:ENSG00000177595 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs10902221 Functional Loss SNV ICGC,COSMIC 33..33 33 bile_duct adenocarcinoma,thyroid neoplasm,biliary_tract adenocarcinoma,colon adenocarcinoma,COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 11 biliary tract,gallbladder,head and neck,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_3938810,Human_RBP_ID_9361879,Human_RBP_ID_18973142 Human_Splice_Rec_1195524,Human_Splice_Rec_1195548,Human_Splice_Rec_1195574,Human_Splice_Rec_1195602,Human_Splice_Rec_1195624,Human_Splice_Rec_1195648,Human_Splice_Rec_1195664 GWAS_ID_6805,GWAS_ID_6806,GWAS_ID_6807,GWAS_ID_6808,GWAS_ID_6809,GWAS_ID_6810,GWAS_ID_6811,GWAS_ID_6812 116667 RMVar_ID_116667 Human_SNP_ID_810962316 m1A Human chr11 + 64854698 64854698 64854698 GTGCCCGAACGGCCCGTTCATGGTGCCGTCAAAGGCGCCGCCCTTGACCACCTGGGAAGGCATCA GTGCCCGAACGGCCCGTTCATGGTGCCGTCAACGGCGCCGCCCTTGACCACCTGGGAAGGCATCA A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64854620..64854720 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116668 RMVar_ID_116668 Human_SNP_ID_810969925 m1A Human chr11 + 2979225 2979225 2979225 CCACTTTGGCTTACCTGTGATCTGCCATCTGAATGTTTTTATCCCCTATAAATTAAAAAGAGTTG CCACTTTGGCTTACCTGTGATCTGCCATCTGACTGTTTTTATCCCCTATAAATTAAAAAGAGTTG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:2978301..2981752 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 116669 RMVar_ID_116669 Human_SNP_ID_810981585 m1A Human chr11 + 18665325 18665325 18665325 ACTGTCCAATGGTGAAAAAAGAAGTAGAAATCATGGCCCACCTCCCTCCTGGGGTCGTCGCCCTC ACTGTCCAATGGTGAAAAAAGAAGTAGAAATCGTGGCCCACCTCCCTCCTGGGGTCGTCGCCCTC A G SRSF3P1 Ensembl:ENSG00000257043 Pseudogene exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs878929748 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_18432562 116670 RMVar_ID_116670 Human_SNP_ID_811003708 m1A Human chr11 - 134276116 134276116 134276116 AGCGGCCCGAGCACAGCCTCACAGCAGATGCGAGCGCGGCGGGCGCTTTGGTGACGAAGTAGCGG AGCGGCCCGAGCACAGCCTCACAGCAGATGCGGGCGCGGCGGGCGCTTTGGTGACGAAGTAGCGG T C lnc-THYN1-1-001 RNACentral:URS00008BE34D lincRNA exon GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs2443557 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116671 RMVar_ID_116671 Human_SNP_ID_811014613 m1A Human chr11 + 61415769 61415769 61415769 TCAAATTCGGCTTCACTCACTGTAGAGGGTGGAGGGCCCGAATCTCGGCTGTACAGAGAAAATAC TCAAATTCGGCTTCACTCACTGTAGAGGGTGGCGGGCCCGAATCTCGGCTGTACAGAGAAAATAC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:61411924..61415802 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 116672 RMVar_ID_116672 Human_SNP_ID_811028980 m1A Human chr11 - 110355262 110355262 110355262 ACCCTCTATTGTACTCTTATCCCTCCTAGCCGACTCCGACCCTGTGTTCCATGAGGAGGCACACG ACCCTCTATTGTACTCTTATCCCTCCTAGCCGCCTCCGACCCTGTGTTCCATGAGGAGGCACACG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:110355213..110355383 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - 116673 RMVar_ID_116673 Human_SNP_ID_811031159 m1A Human chr11 - 77813676 77813676 77813676 GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTATGGCTTTGAAGGTTACCGGAAAAACACGCGTG GAACAAGTCGGTCAGGAAGCCGTGCAGCAGCTCTGGCTTTGAAGGTTACCGGAAAAACACGCGTG T G AP000580.1,RSF1 Ensembl:ENSG00000219529,Ensembl:ENSG00000048649 Pseudogene,Protein coding exon,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:77813636..77813705 26863196 MeRIP-seq:(Medium) rs58914857 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 1 haematopoietic and lymphoid tissue Human_RBP_ID_404295,Human_RBP_ID_866844,Human_RBP_ID_1265958,Human_RBP_ID_9364192,Human_RBP_ID_19050338 Human_Splice_Rec_1281504 GWAS_ID_9379,GWAS_ID_9380,GWAS_ID_9381,GWAS_ID_9382,GWAS_ID_9383,GWAS_ID_9384,GWAS_ID_9385,GWAS_ID_9386,GWAS_ID_9387,GWAS_ID_9388,GWAS_ID_9389,GWAS_ID_9390,GWAS_ID_9391,GWAS_ID_9392,GWAS_ID_9393,GWAS_ID_9394,GWAS_ID_9395,GWAS_ID_9396,GWAS_ID_9397,GWAS_ID_9398,GWAS_ID_9399,GWAS_ID_9400,GWAS_ID_9401,GWAS_ID_9402,GWAS_ID_9403,GWAS_ID_9404,GWAS_ID_9405,GWAS_ID_9406,GWAS_ID_9407,GWAS_ID_9408,GWAS_ID_9409,GWAS_ID_9410,GWAS_ID_9411,GWAS_ID_9412,GWAS_ID_9413,GWAS_ID_9414,GWAS_ID_9415,GWAS_ID_9416,GWAS_ID_9417,GWAS_ID_9418,GWAS_ID_9419,GWAS_ID_9420,GWAS_ID_9421,GWAS_ID_9422,GWAS_ID_9423,GWAS_ID_9424,GWAS_ID_9425,GWAS_ID_9426,GWAS_ID_9427,GWAS_ID_9428,GWAS_ID_9429,GWAS_ID_9430,GWAS_ID_9431,GWAS_ID_9432,GWAS_ID_9433,GWAS_ID_9434,GWAS_ID_9435,GWAS_ID_9436,GWAS_ID_9437,GWAS_ID_9438 116674 RMVar_ID_116674 Human_SNP_ID_811042613 m1A Human chr11 - 17509574 17509574 17509574 TGAGCGCCTCATCCTCTCCATGGGTGCAGCGCACTCCACCCCCCATTCCCATCCCTCCCCCGCCA TGAGCGCCTCATCCTCTCCATGGGTGCAGCGCTCTCCACCCCCCATTCCCATCCCTCCCCCGCCA T A USH1C Ensembl:ENSG00000006611 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:17509573..17509777 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 116675 RMVar_ID_116675 Human_SNP_ID_811068372 m1A Human chr11 + 62678400 62678400 62678400 ACTCAAAGCGGGTTTGCCTTCTCCGGCAGCAGAACCAGATCCTACAAACAAACAATCGGTATTAT ACTCAAAGCGGGTTTGCCTTCTCCGGCAGCAGTACCAGATCCTACAAACAAACAATCGGTATTAT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62678326..62678433 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 116676 RMVar_ID_116676 Human_SNP_ID_811107187 m1A Human chr11 - 62841780 62841780 62841780 GGTATCGCTTCTCGGCCTTTTGGCTAAGATCAAGTGTAGTATCTGTTCTTATCAGTTTAATATCT GGTATCGCTTCTCGGCCTTTTGGCTAAGATCACGTGTAGTATCTGTTCTTATCAGTTTAATATCT T G WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus Human_RBP_ID_108215,Human_RBP_ID_399282,Human_RBP_ID_5086780,Human_RBP_ID_5093729,Human_RBP_ID_5554310,Human_RBP_ID_9004662,Human_RBP_ID_11660362,Human_RBP_ID_17351276,Human_RBP_ID_18174124,Human_RBP_ID_18198710,Human_RBP_ID_18205804,Human_RBP_ID_19651987,Human_RBP_ID_21966908,Human_RBP_ID_22569318,Human_RBP_ID_22641368,Human_RBP_ID_22736055,Human_RBP_ID_22791013,Human_RBP_ID_23110222,Human_RBP_ID_23511360,Human_RBP_ID_26405008,Human_RBP_ID_26747655,Human_RBP_ID_26776752,Human_RBP_ID_26893089,Human_RBP_ID_27203651,Human_RBP_ID_27413258 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 116677 RMVar_ID_116677 Human_SNP_ID_811113166 m1A Human chr11 - 57332232 57332224 57332232 CGCTTTGAGGGTCGGCTCACCAAGAACATGTCAGGATCCCTCTATGAGATGGTCAGCCGGGTCAT CGCTTTGAGGGTCGGCTCACCAAGAACATGTC________TCTATGAGATGGTCAGCCGGGTCAT AGGGATCCT A SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57332130..57332293 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..40 33 LICA 1 - Human_RBP_ID_226653,Human_RBP_ID_987306,Human_RBP_ID_1779930,Human_RBP_ID_4163026,Human_RBP_ID_8769850,Human_RBP_ID_9276318,Human_RBP_ID_11642358,Human_RBP_ID_17232287,Human_RBP_ID_18973618,Human_RBP_ID_22891177,Human_RBP_ID_26318329,Human_RBP_ID_26803434 Human_Splice_Rec_1239498,Human_Splice_Rec_1239499,Human_Splice_Rec_1239524,Human_Splice_Rec_1239525 Human_miRNA_ID_2534553,Human_miRNA_ID_2536286 RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_121817,RMVar_hsa_circ_110723,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_14433,RMVar_hsa_circ_149735,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_78264,RMVar_hsa_circ_111815,RMVar_hsa_circ_79048,RMVar_hsa_circ_149748,RMVar_hsa_circ_149749,RMVar_hsa_circ_149747,RMVar_hsa_circ_65327,RMVar_hsa_circ_70172 116678 RMVar_ID_116678 Human_SNP_ID_811138376 m1A Human chr11 - 47722931 47722931 47722931 TCCCTTTTTAAAAATTTATTTTTAAAAATTTTATTGAGGTTATATTCACATAACATGAAATTATC TCCCTTTTTAAAAATTTATTTTTAAAAATTTTTTTGAGGTTATATTCACATAACATGAAATTATC T A FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47722929..47723125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_72508,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_317026,RMVar_hsa_circ_378749,RMVar_hsa_circ_149622 116679 RMVar_ID_116679 Human_SNP_ID_811144293 m1A Human chr11 + 66020348 66020348 66020348 CCTCCTGCTTCGCTTTCTCAAGGCCTTTGAACAGCGCCGTCTGGAAGCTATCCACCAGGACAGTA CCTCCTGCTTCGCTTTCTCAAGGCCTTTGAACTGCGCCGTCTGGAAGCTATCCACCAGGACAGTA A T RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66020142..66020865 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 116680 RMVar_ID_116680 Human_SNP_ID_811147153 m1A Human chr11 + 774097 774097 774097 CCCAGCGTGCATTGCTCTCAGTCACATCCACAAATTCCATGGCTTTCCCCTGGAGAAGCAGAGCC CCCAGCGTGCATTGCTCTCAGTCACATCCACACATTCCATGGCTTTCCCCTGGAGAAGCAGAGCC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:773509..775087 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 116681 RMVar_ID_116681 Human_SNP_ID_811163201 m1A Human chr11 - 113773666 113773666 113773666 TGACCCAGTCAGCGTTGGTTCCCGTCTTGGCCATGGCCTCGTTCGTGACAGAAGTTTTGGCACAC TGACCCAGTCAGCGTTGGTTCCCGTCTTGGCCGTGGCCTCGTTCGTGACAGAAGTTTTGGCACAC T C ZW10 Ensembl:ENSG00000086827 Protein coding start codon GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:113773621..113773708 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_389112,Human_RBP_ID_4185385,Human_RBP_ID_23487058,Human_RBP_ID_26804088 RMVar_hsa_circ_109625,RMVar_hsa_circ_153149 116682 RMVar_ID_116682 Human_SNP_ID_811174015 m1A Human chr11 - 60927234 60927234 60927234 CGTCTAGGAGCTCCAGGGCTGCCGGCAGGTAGACAGGGTCCAGGGGAGCCTGGCCACAGTCCACT CGTCTAGGAGCTCCAGGGCTGCCGGCAGGTAGGCAGGGTCCAGGGGAGCCTGGCCACAGTCCACT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:60927197..60927422 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck 116683 RMVar_ID_116683 Human_SNP_ID_811180622 m1A Human chr11 + 314175 314175 314175 TCAACACTTCCTTCCCCAAAGCCAGAAGATGCACAAGGAGGAACATGAGGTGGCTGTGCTGGGGC TCAACACTTCCTTCCCCAAAGCCAGAAGATGCGCAAGGAGGAACATGAGGTGGCTGTGCTGGGGC A G IFITM2,IFITM1 Ensembl:ENSG00000185201,Ensembl:ENSG00000185885 Protein coding,Protein coding intron,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:314126..314200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_17233701 Human_Splice_Rec_1192620 RMVar_hsa_circ_127511,RMVar_hsa_circ_147373 116684 RMVar_ID_116684 Human_SNP_ID_811181522 m1A Human chr11 - 57326462 57326460 57326463 CACCTTTGGTTTTCAGGACTCTGAAGAAGAAGAACTAGCCAGTACTCCCCCCAGCTCAGAGGACT CACCTTTGGTTTTCAGGACTCTGAAGAAGAA___CTAGCCAGTACTCCCCCCAGCTCAGAGGACT GTTC G SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:57326232..57326495 26863196 MeRIP-seq:(Medium) rs764601446 Functional Loss DEL TCGA 32..34 33 STAD 1 - Human_RBP_ID_30713,Human_RBP_ID_226645,Human_RBP_ID_870808,Human_RBP_ID_1457474,Human_RBP_ID_1779906,Human_RBP_ID_6078805,Human_RBP_ID_9362235,Human_RBP_ID_11642244,Human_RBP_ID_19051560,Human_RBP_ID_22570994,Human_RBP_ID_23508632,Human_RBP_ID_26318311 Human_Splice_Rec_1239510,Human_Splice_Rec_1239542 Human_miRNA_ID_1993554 RMVar_hsa_circ_84817,RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_113781,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149744,RMVar_hsa_circ_149745,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732 116685 RMVar_ID_116685 Human_SNP_ID_811184329 m1A Human chr11 - 60898621 60898621 60898621 CACAGGTCTCTCTTCCCTCCTCCACAGCTCTCACCTGTGCACAGTTCCACCCTGACGGACTCATC CACAGGTCTCTCTTCCCTCCTCCACAGCTCTCGCCTGTGCACAGTTCCACCCTGACGGACTCATC T C PRPF19 Ensembl:ENSG00000110107 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:60898576..60898650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_19051634,Human_RBP_ID_22641218 Human_Splice_Rec_1244196,Human_Splice_Rec_1244197,Human_Splice_Rec_1244210,Human_Splice_Rec_1244211,Human_Splice_Rec_1244218,Human_Splice_Rec_1244219 RMVar_hsa_circ_63437,RMVar_hsa_circ_124507,RMVar_hsa_circ_125655,RMVar_hsa_circ_122566,RMVar_hsa_circ_149887,RMVar_hsa_circ_88650,RMVar_hsa_circ_93405,RMVar_hsa_circ_149889,RMVar_hsa_circ_81564,RMVar_hsa_circ_149890,RMVar_hsa_circ_149888,RMVar_hsa_circ_149885,RMVar_hsa_circ_149886,RMVar_hsa_circ_41677,RMVar_hsa_circ_29763 116686 RMVar_ID_116686 Human_SNP_ID_811189029 m1A Human chr11 - 124636167 124636167 124636167 GTGACTGCCCTAAGGAATGAAAAGCAAGGGCCAGGTGGGAGTAGCCCAGCGAAGGCACTTGGGCT GTGACTGCCCTAAGGAATGAAAAGCAAGGGCCGGGTGGGAGTAGCCCAGCGAAGGCACTTGGGCT T C SIAE Ensembl:ENSG00000110013 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:124636118..124636192 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_153824,RMVar_hsa_circ_101927 116687 RMVar_ID_116687 Human_SNP_ID_811190797 m1A Human chr11 - 59182030 59182030 59182030 CAGGGCTGACTGGCCAGGACTGAGCCTTAGGCAAGGTCCCTGTGACCATGGGGTAGATGAGGTCG CAGGGCTGACTGGCCAGGACTGAGCCTTAGGCGAGGTCCCTGTGACCATGGGGTAGATGAGGTCG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:59181985..59182120 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung 116688 RMVar_ID_116688 Human_SNP_ID_811200236 m1A Human chr11 - 63763836 63763836 63763836 CGACGTTCCGCTGTCCCCTGGAGCTCCCTTGGAGCGGCCCGCCGAAGAAGAGGAGGACGAAGAGG CGACGTTCCGCTGTCCCCTGGAGCTCCCTTGGTGCGGCCCGCCGAAGAAGAGGAGGACGAAGAGG T A C11orf95 Ensembl:ENSG00000188070 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:63763739..63764258 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5139324 Human_Splice_Rec_1251756,Human_Splice_Rec_1251758 RMVar_hsa_circ_99504,RMVar_hsa_circ_150369 116689 RMVar_ID_116689 Human_SNP_ID_811204811 m1A Human chr11 - 862921 862921 862921 CCACACCGCTCTGCAAATCACCCCCCAGCCCCAGTGTGGCCTGGAAGACCCAACAGTGGCCAGGG CCACACCGCTCTGCAAATCACCCCCCAGCCCCCGTGTGGCCTGGAAGACCCAACAGTGGCCAGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:862919..863020 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 11 liver Human_RBP_ID_23525298 116690 RMVar_ID_116690 Human_SNP_ID_811210465 m1A Human chr11 + 67071832 67071832 67071832 CTCGTCCTGCGGTGCCCGAGAATCACTCGCTAACCCCTATGCCCGGTCCCGGACCGACATCCTGG CTCGTCCTGCGGTGCCCGAGAATCACTCGCTACCCCCTATGCCCGGTCCCGGACCGACATCCTGG A C RHOD Ensembl:ENSG00000173156 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67071783..67071932 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_101729,RMVar_hsa_circ_151011 116691 RMVar_ID_116691 Human_SNP_ID_811232084 m1A Human chr11 - 66052674 66052674 66052674 CTCTGCAGCCGCTCCACCAGCTCCTCGCGATTACCTGCAGGGCAAAGTACACGATCAATGGGGCA CTCTGCAGCCGCTCCACCAGCTCCTCGCGATTGCCTGCAGGGCAAAGTACACGATCAATGGGGCA T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66052380..66052759 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - 116692 RMVar_ID_116692 Human_SNP_ID_811235746 m1A Human chr11 + 66220719 66220719 66220719 CTTGGATGAATTGTATGACAGTCTGGAGATGTACAACCCCAGCGACAGTGGCCCTGAGATGGAGG CTTGGATGAATTGTATGACAGTCTGGAGATGTGCAACCCCAGCGACAGTGGCCCTGAGATGGAGG A G PACS1 Ensembl:ENSG00000175115 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66220669..66220819 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_RBP_ID_4173386,Human_RBP_ID_9362598,Human_RBP_ID_27804768 Human_Splice_Rec_1261680,Human_Splice_Rec_1261681,Human_Splice_Rec_1261746,Human_Splice_Rec_1261754,Human_Splice_Rec_1261755,Human_Splice_Rec_1261757,Human_Splice_Rec_1261759 RMVar_hsa_circ_35747,RMVar_hsa_circ_101287,RMVar_hsa_circ_150828,RMVar_hsa_circ_83761,RMVar_hsa_circ_77681,RMVar_hsa_circ_95449,RMVar_hsa_circ_121403,RMVar_hsa_circ_150831,RMVar_hsa_circ_150832,RMVar_hsa_circ_349192,RMVar_hsa_circ_150836,RMVar_hsa_circ_120117,RMVar_hsa_circ_150835,RMVar_hsa_circ_48865,RMVar_hsa_circ_89695,RMVar_hsa_circ_150839,RMVar_hsa_circ_106903,RMVar_hsa_circ_150840,RMVar_hsa_circ_150841,RMVar_hsa_circ_150842,RMVar_hsa_circ_97458,RMVar_hsa_circ_150843 116693 RMVar_ID_116693 Human_SNP_ID_811238970 m1A Human chr11 - 73981634 73981634 73981634 CCTTTCTAAACTCTCTGCCTTTGCTCACCCACAGGACACATAGTATGACCATTAGGTGTTTCGTC CCTTTCTAAACTCTCTGCCTTTGCTCACCCACCGGACACATAGTATGACCATTAGGTGTTTCGTC T G UCP2 Ensembl:ENSG00000175567 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:73981601..73981650 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach Human_RBP_ID_22643737 RMVar_hsa_circ_125553,RMVar_hsa_circ_151650 116694 RMVar_ID_116694 Human_SNP_ID_811282273 m1A Human chr11 + 66058268 66058268 66058268 CTTGGTAAAGGCAGGTTACTGTGAACGAGTGCAGGGCAGTGGCACCGTGAAGACTCATCACCACC CTTGGTAAAGGCAGGTTACTGTGAACGAGTGCGGGGCAGTGGCACCGTGAAGACTCATCACCACC A G SF3B2 Ensembl:ENSG00000087365 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66058266..66058432 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_11676258 RMVar_hsa_circ_74717,RMVar_hsa_circ_14810,RMVar_hsa_circ_339833,RMVar_hsa_circ_14280,RMVar_hsa_circ_150818,RMVar_hsa_circ_150819,RMVar_hsa_circ_93752 116695 RMVar_ID_116695 Human_SNP_ID_811283990 m1A Human chr11 + 71442312 71442312 71442312 CCCTCCTGGATGCCTCCTACGTAGCCGGGTAGAAACTTATGGCAGAAGTCAGGGAGAGACGTGTA CCCTCCTGGATGCCTCCTACGTAGCCGGGTAGGAACTTATGGCAGAAGTCAGGGAGAGACGTGTA A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:71442217..71442397 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 116696 RMVar_ID_116696 Human_SNP_ID_811290289 m1A Human chr11 - 119094994 119094994 119094994 CACCGTGGGGCCGAAGGCGCCCTCGGGCGGCAAGAAGGCCACCCAGGCCTCCCAGGAGTACTAAG CACCGTGGGGCCGAAGGCGCCCTCGGGCGGCAGGAAGGCCACCCAGGCCTCCCAGGAGTACTAAG T C H2AX Ensembl:ENSG00000188486 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:119094976..119095000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_32694,Human_RBP_ID_751777,Human_RBP_ID_3941316,Human_RBP_ID_4188381,Human_RBP_ID_5110646,Human_RBP_ID_9363027,Human_RBP_ID_17681402,Human_RBP_ID_17790997,Human_RBP_ID_22755091,Human_RBP_ID_22789738,Human_RBP_ID_26317869,Human_RBP_ID_26804166,Human_RBP_ID_26886748,Human_RBP_ID_27198604 116697 RMVar_ID_116697 Human_SNP_ID_811300759 m1A Human chr11 - 1461120 1461120 1461120 CTTCCTCCCACGGGCCGTGCGGAGCTGAGGCGAGGAGCTGCCGCGGGGTGGACGGGGCGCTGGGC CTTCCTCCCACGGGCCGTGCGGAGCTGAGGCGGGGAGCTGCCGCGGGGTGGACGGGGCGCTGGGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:1460943..1461403 26863196 MeRIP-seq:(Medium) rs139099614 Functional Loss SNV ICGC 33..33 33 BOCA 1 - 116698 RMVar_ID_116698 Human_SNP_ID_811312941 m1A Human chr11 - 47753061 47753061 47753061 GCCATAACAGCTCCTCAGCCTGCAGCTCCTGTAGGAGCTTCTGCTCCACCTCCAACTCCACCTCG GCCATAACAGCTCCTCAGCCTGCAGCTCCTGTGGGAGCTTCTGCTCCACCTCCAACTCCACCTCG T C FNBP4 Ensembl:ENSG00000109920 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47753015..47753090 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach Human_RBP_ID_29746,Human_RBP_ID_9363582,Human_RBP_ID_18608583 Human_Splice_Rec_1238254,Human_Splice_Rec_1238324,Human_Splice_Rec_1238348,Human_Splice_Rec_1238350,Human_Splice_Rec_1238352 RMVar_hsa_circ_5588,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_44057,RMVar_hsa_circ_79080,RMVar_hsa_circ_280985,RMVar_hsa_circ_347418,RMVar_hsa_circ_149630,RMVar_hsa_circ_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_354843,RMVar_hsa_circ_359423,RMVar_hsa_circ_68679,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_58118,RMVar_hsa_circ_319392,RMVar_hsa_circ_298577,RMVar_hsa_circ_149646,RMVar_hsa_circ_149647,RMVar_hsa_circ_118663,RMVar_hsa_circ_273731,RMVar_hsa_circ_149648,RMVar_hsa_circ_149649,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304 116699 RMVar_ID_116699 Human_SNP_ID_811322823 m1A Human chr11 - 119055573 119055573 119055573 GCAGGCACCTGGGCCCAAAATCTCTTTTCCTCAGGGAATCTCGGAGGAAAACACCGGTGATCGTG GCAGGCACCTGGGCCCAAAATCTCTTTTCCTCGGGGAATCTCGGAGGAAAACACCGGTGATCGTG T C HYOU1 Ensembl:ENSG00000149428 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:119055551..119055575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 13 pancreas Human_RBP_ID_4188324,Human_RBP_ID_19054329,Human_RBP_ID_22642066,Human_RBP_ID_23529895,Human_RBP_ID_24871909 Human_Splice_Rec_1306237,Human_Splice_Rec_1306287,Human_Splice_Rec_1306321,Human_Splice_Rec_1306333,Human_Splice_Rec_1306381,Human_Splice_Rec_1306431,Human_Splice_Rec_1306469,Human_Splice_Rec_1306519,Human_Splice_Rec_1306557,Human_Splice_Rec_1306595,Human_Splice_Rec_1306607,Human_Splice_Rec_1306617,Human_Splice_Rec_1306627,Human_Splice_Rec_1306637,Human_Splice_Rec_1306645,Human_Splice_Rec_1306655,Human_Splice_Rec_1306659,Human_Splice_Rec_1306669,Human_Splice_Rec_1306679 RMVar_hsa_circ_66064 116700 RMVar_ID_116700 Human_SNP_ID_811323952 m1A Human chr11 + 92224755 92224755 92224755 TGCGAGAGACAAGCGCGAGGGGGAGACTGGAGAGGGGCTTGGCCGTGCGTCGGCGTCGGCTGTGA TGCGAGAGACAAGCGCGAGGGGGAGACTGGAGCGGGGCTTGGCCGTGCGTCGGCGTCGGCTGTGA A C HSALNG0086425 RNACentral:URS0000EB9076 lincRNA intron GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:92224654..92224844 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 116701 RMVar_ID_116701 Human_SNP_ID_811330933 m1A Human chr11 + 8806015 8806015 8806015 CTTCTGAGGGCCTGCACGACACTGTCACCCTGAGCTCCCTGGGGGCAGTCTGGCCTTCTGCTAAA CTTCTGAGGGCCTGCACGACACTGTCACCCTGCGCTCCCTGGGGGCAGTCTGGCCTTCTGCTAAA A C AC026894.3 Ensembl:ENSG00000255159 lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:8806009..8806234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 116702 RMVar_ID_116702 Human_SNP_ID_811338303 m1A Human chr11 - 119310468 119310468 119310468 GATACCAACCTCTCACCTCCCTCCCTCCTCCCAGCACGCTACCCCCGTCTCGTAAGAGCGAACTT GATACCAACCTCTCACCTCCCTCCCTCCTCCCTGCACGCTACCCCCGTCTCGTAAGAGCGAACTT T A MCAM Ensembl:ENSG00000076706 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119310356..119310477 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_RBP_ID_27409605 RMVar_hsa_circ_113856,RMVar_hsa_circ_153540 116703 RMVar_ID_116703 Human_SNP_ID_811343011 m1A Human chr11 + 1557213 1557213 1557213 GCTAGGGGCGTAGGCAGACTTGATGTCCAGGGAGAAGGAGCGCTTGAGGCGGTTAGTGTCCTGCA GCTAGGGGCGTAGGCAGACTTGATGTCCAGGGGGAAGGAGCGCTTGAGGCGGTTAGTGTCCTGCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:1557162..1557305 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116704 RMVar_ID_116704 Human_SNP_ID_811354848 m1A Human chr11 - 67501995 67501995 67501995 CCCCGGCTTTATCACTCGGTCAAGACGGGCCGAGGGCCACTGTCTGATGACTGGGCACGGACGGC CCCCGGCTTTATCACTCGGTCAAGACGGGCCGGGGGCCACTGTCTGATGACTGGGCACGGACGGC T C PITPNM1 Ensembl:ENSG00000110697 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67501951..67502100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,lung non_small_cell_carcinoma 6 lung,kidney Human_RBP_ID_17800073 Human_Splice_Rec_1266770,Human_Splice_Rec_1266814,Human_Splice_Rec_1266858,Human_Splice_Rec_1266944,Human_Splice_Rec_1266952,Human_Splice_Rec_1266960 RMVar_hsa_circ_594,RMVar_hsa_circ_80744,RMVar_hsa_circ_151072,RMVar_hsa_circ_124441,RMVar_hsa_circ_151075,RMVar_hsa_circ_104213,RMVar_hsa_circ_151077 116705 RMVar_ID_116705 Human_SNP_ID_811358444 m1A Human chr11 + 62630713 62630713 62630713 TGCCATCAGCATGTTCAATGTCTAGCCAGATGACATCACAGGGCAGGTTGTGATCATCAAAGCCC TGCCATCAGCATGTTCAATGTCTAGCCAGATGGCATCACAGGGCAGGTTGTGATCATCAAAGCCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62630595..62630712 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate 116706 RMVar_ID_116706 Human_SNP_ID_811364780 m1A Human chr11 + 68036564 68036564 68036564 ACGGGGACAAGTGGGAGGCCGAGATCGCCGCCAACATCCAGGCTGACTACTTGTATCGGTGACGC ACGGGGACAAGTGGGAGGCCGAGATCGCCGCCGACATCCAGGCTGACTACTTGTATCGGTGACGC A G NDUFS8 Ensembl:ENSG00000110717 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:68036364..68036650 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_402216,Human_RBP_ID_988212,Human_RBP_ID_1459829,Human_RBP_ID_9005770,Human_RBP_ID_17649219 RMVar_hsa_circ_79704,RMVar_hsa_circ_151101,RMVar_hsa_circ_108670,RMVar_hsa_circ_91696,RMVar_hsa_circ_128022,RMVar_hsa_circ_151104,RMVar_hsa_circ_119067,RMVar_hsa_circ_151105,RMVar_hsa_circ_151106,RMVar_hsa_circ_151107 116707 RMVar_ID_116707 Human_SNP_ID_811370577 m1A Human chr11 + 72695447 72695447 72695447 TTCTCTTCCAGATACACTGTGCAGATGAAGTCACCGGCATGCTGCAGGGAGACAGGGCTCAGCTG TTCTCTTCCAGATACACTGTGCAGATGAAGTCGCCGGCATGCTGCAGGGAGACAGGGCTCAGCTG A G AP003065.2 Ensembl:ENSG00000286555 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72693239..72695642 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 7 large intestine Human_Splice_Rec_1275298 116708 RMVar_ID_116708 Human_SNP_ID_811375147 m1A Human chr11 + 65297331 65297331 65297331 GTGGGCCCTTAAAGTCTTAGCCAAGAGCCAAGACATAGCCCTGTGACAAGGTGAACAGTTGGGTG GTGGGCCCTTAAAGTCTTAGCCAAGAGCCAAGGCATAGCCCTGTGACAAGGTGAACAGTTGGGTG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65297280..65297470 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_miRNA_ID_1264353,Human_miRNA_ID_2777654 RMVar_hsa_circ_88335,RMVar_hsa_circ_150611,RMVar_hsa_circ_97700,RMVar_hsa_circ_150622 116709 RMVar_ID_116709 Human_SNP_ID_811382367 m1A Human chr11 - 117228296 117228296 117228296 GGGACATCAACGTGACGGGTGTGTGGGAACGCAATGTGACTGGGCGAGGGGTGACGGTGGTGGTA GGGACATCAACGTGACGGGTGTGTGGGAACGCGATGTGACTGGGCGAGGGGTGACGGTGGTGGTA T C PCSK7 Ensembl:ENSG00000160613 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117228196..117228409 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_226793,Human_RBP_ID_3941255,Human_RBP_ID_18972781,Human_RBP_ID_26319240 Human_Splice_Rec_1301764,Human_Splice_Rec_1301765,Human_Splice_Rec_1301816,Human_Splice_Rec_1301817,Human_Splice_Rec_1301878,Human_Splice_Rec_1301879 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294,RMVar_hsa_circ_268971 116710 RMVar_ID_116710 Human_SNP_ID_811383665 m1A Human chr11 + 68372454 68372454 68372454 CCGTGGCGGCGAGGAGGTGCAGCGTCAGGCGGACCCGGGACCGTGGCGGCGAGGAGGTGCAGTGT CCGTGGCGGCGAGGAGGTGCAGCGTCAGGCGGTCCCGGGACCGTGGCGGCGAGGAGGTGCAGTGT A T LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:68372165..68372499;chr11:68372076..68372561;chr11:68372033..68372555;chr11:68372112..68372528 26863196 MeRIP-seq:(Medium) rs314777 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_806445,Human_RBP_ID_3386995,Human_RBP_ID_8063678,Human_RBP_ID_8174505,Human_RBP_ID_17111150,Human_RBP_ID_18416957,Human_RBP_ID_22709599 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_151178,RMVar_hsa_circ_151180 116711 RMVar_ID_116711 Human_SNP_ID_811388280 m1A Human chr11 + 65885580 65885578 65885580 AGTTTTGGATCATGAGCTCAGCGCAGAAGGCAAAGTCACCGAAGCTCAGATACTGCAGTTTTTTC AGTTTTGGATCATGAGCTCAGCGCAGAAGGC__AGTCACCGAAGCTCAGATACTGCAGTTTTTTC CAA C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65885444..65885650 32194978 MeRIP-seq:(Medium) rs1565281237 Functional Loss DEL TCGA 32..33 33 STAD 1 - 116712 RMVar_ID_116712 Human_SNP_ID_811390031 m1A Human chr11 + 68036380 68036380 68036380 CCAGGAGGCCTGTCCCGTGGATGCCATCGTCGAGGCACGTGAGGCCCCCGGGTGGGAGGGGGCCT CCAGGAGGCCTGTCCCGTGGATGCCATCGTCGGGGCACGTGAGGCCCCCGGGTGGGAGGGGGCCT A G NDUFS8 Ensembl:ENSG00000110717 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:68036351..68036650;chr11:68036093..68036439;chr11:68036365..68036453 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_749349,Human_RBP_ID_5460742,Human_RBP_ID_17649217,Human_RBP_ID_26803919 RMVar_hsa_circ_15030,RMVar_hsa_circ_79704,RMVar_hsa_circ_151101,RMVar_hsa_circ_91696,RMVar_hsa_circ_128022,RMVar_hsa_circ_151104,RMVar_hsa_circ_119067,RMVar_hsa_circ_151105,RMVar_hsa_circ_151106 116713 RMVar_ID_116713 Human_SNP_ID_811390972 m1A Human chr11 - 842627 842627 842627 GCGGTGGCGGGGCCGGTGGAGGGACGGCCGGAACAGCGGAGAACGAGCGGAGCCGATTCTCCCGC GCGGTGGCGGGGCCGGTGGAGGGACGGCCGGAGCAGCGGAGAACGAGCGGAGCCGATTCTCCCGC T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:842576..842766 26863196 MeRIP-seq:(Medium) rs9705236 Functional Loss SNV ICGC 33..33 33 COCA 1 - 116714 RMVar_ID_116714 Human_SNP_ID_811392143 m1A Human chr11 + 319776 319776 319776 GACTCGGCTCCGGGGGCAGGGCGAGGAATGGAAGTTGGAGTACGTGGGATACAGGTCATGGGCAG GACTCGGCTCCGGGGGCAGGGCGAGGAATGGACGTTGGAGTACGTGGGATACAGGTCATGGGCAG A C AC136475.1 Ensembl:ENSG00000251661 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:319676..319950;chr11:319676..319914 26863196 MeRIP-seq:(Medium) rs1166426553 Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_3388428,Human_RBP_ID_5553059 116715 RMVar_ID_116715 Human_SNP_ID_811407099 m1A Human chr11 + 964867 964867 964867 TAAAGGAAATAATCCCAGATGGAAGCGTGGAGATGGAAAGCATGGAACGGGCGGGAAATTAAAGG TAAAGGAAATAATCCCAGATGGAAGCGTGGAGGTGGAAAGCATGGAACGGGCGGGAAATTAAAGG A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:964807..964908;chr11:964816..964933 26863196 MeRIP-seq:(Medium) rs7396338 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_292644 116716 RMVar_ID_116716 Human_SNP_ID_811411046 m1A Human chr11 - 18519602 18519602 18519602 AACTAAATTCTTATGCGATTTTGCTTTTCAGTACAAATACAGAGACCTAACTGTACGTGAAACTG AACTAAATTCTTATGCGATTTTGCTTTTCAGTGCAAATACAGAGACCTAACTGTACGTGAAACTG T C TSG101 Ensembl:ENSG00000074319 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:18519551..18519625;chr11:18519551..18519677 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_4184703 Human_Splice_Rec_1219078,Human_Splice_Rec_1219079,Human_Splice_Rec_1219106,Human_Splice_Rec_1219107,Human_Splice_Rec_1219126,Human_Splice_Rec_1219127,Human_Splice_Rec_1219176,Human_Splice_Rec_1219177 Human_miRNA_ID_2922496 RMVar_hsa_circ_91752,RMVar_hsa_circ_148605,RMVar_hsa_circ_148606,RMVar_hsa_circ_310762,RMVar_hsa_circ_148609,RMVar_hsa_circ_148614,RMVar_hsa_circ_319373,RMVar_hsa_circ_287309,RMVar_hsa_circ_273523 116717 RMVar_ID_116717 Human_SNP_ID_811432784 m1A Human chr11 - 69673297 69673297 69673297 CTTCACAGGTTTCATGGGGAAGGGTATCGGGAAGGCTATGAAGAAGGCAGTAGTTTGGGTGTGAT CTTCACAGGTTTCATGGGGAAGGGTATCGGGAGGGCTATGAAGAAGGCAGTAGTTTGGGTGTGAT T C LTO1 Ensembl:ENSG00000149716 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:69673246..69673366 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_752358,Human_RBP_ID_21966652,Human_RBP_ID_22895742 Human_Splice_Rec_1270002,Human_Splice_Rec_1270003,Human_Splice_Rec_1270011,Human_Splice_Rec_1270022,Human_Splice_Rec_1270023,Human_Splice_Rec_1270042,Human_Splice_Rec_1270043,Human_Splice_Rec_1270058,Human_Splice_Rec_1270059,Human_Splice_Rec_1270078,Human_Splice_Rec_1270079,Human_Splice_Rec_1270084,Human_Splice_Rec_1270085,Human_Splice_Rec_1270092,Human_Splice_Rec_1270093,Human_Splice_Rec_1270096,Human_Splice_Rec_1270098 RMVar_hsa_circ_48671,RMVar_hsa_circ_40424,RMVar_hsa_circ_151350,RMVar_hsa_circ_151351,RMVar_hsa_circ_59293,RMVar_hsa_circ_314073,RMVar_hsa_circ_360695 116718 RMVar_ID_116718 Human_SNP_ID_811442500 m1A Human chr11 - 118638914 118638914 118638914 TGCACGGCCTGAGCCCGGATCTGCCCAGCCTGACTGTCCAGGATGGCCAGGCGCTCCTAAAGGAG TGCACGGCCTGAGCCCGGATCTGCCCAGCCTGCCTGTCCAGGATGGCCAGGCGCTCCTAAAGGAG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118635522..118639175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 116719 RMVar_ID_116719 Human_SNP_ID_811451241 m1A Human chr11 + 63939067 63939065 63939068 GCCGTTGCCGCCTCCCTGCCGGCAAGTGTGTGAAGAAGAAGCTGAGCGTTGTCGCCGCCGCTATG GCCGTTGCCGCCTCCCTGCCGGCAAGTGTGT___GAAGAAGCTGAGCGTTGTCGCCGCCGCTATG TGAA T NAA40 Ensembl:ENSG00000110583 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:63939016..63939156 26863196 MeRIP-seq:(Medium) rs746521848 Functional Loss DEL ICGC 32..34 33 CHOL 1 - Human_RBP_ID_807339,Human_RBP_ID_4168329,Human_RBP_ID_5549560,Human_RBP_ID_9362401,Human_RBP_ID_18416573,Human_RBP_ID_24542655 Human_Splice_Rec_1252159,Human_Splice_Rec_1252171,Human_Splice_Rec_1252179,Human_Splice_Rec_1252191,Human_Splice_Rec_1252199,Human_Splice_Rec_1252207 Human_miRNA_ID_2539859,Human_miRNA_ID_2909255 RMVar_hsa_circ_83810,RMVar_hsa_circ_150390 116720 RMVar_ID_116720 Human_SNP_ID_811454141 m1A Human chr11 + 850341 850341 850341 CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCATGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT CGCGCGCCTGCCTCCAGGCCGTCAAGTACCTCGTGTTCGCCTTCAACCTGCTCTTCTGGGTGAGT A G TSPAN4 Ensembl:ENSG00000214063 Protein coding CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:850276..850375 26863196 MeRIP-seq:(Medium) rs763642214 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 12 stomach Human_RBP_ID_4184578 Human_Splice_Rec_1196098,Human_Splice_Rec_1196099,Human_Splice_Rec_1196128,Human_Splice_Rec_1196129,Human_Splice_Rec_1196144,Human_Splice_Rec_1196145,Human_Splice_Rec_1196160,Human_Splice_Rec_1196161,Human_Splice_Rec_1196176,Human_Splice_Rec_1196177,Human_Splice_Rec_1196190,Human_Splice_Rec_1196191,Human_Splice_Rec_1196218,Human_Splice_Rec_1196219,Human_Splice_Rec_1196232,Human_Splice_Rec_1196233,Human_Splice_Rec_1196236,Human_Splice_Rec_1196237,Human_Splice_Rec_1196240,Human_Splice_Rec_1196241,Human_Splice_Rec_1196250,Human_Splice_Rec_1196251,Human_Splice_Rec_1196262,Human_Splice_Rec_1196263,Human_Splice_Rec_1196270,Human_Splice_Rec_1196271,Human_Splice_Rec_1196283 RMVar_hsa_circ_296316,RMVar_hsa_circ_317179,RMVar_hsa_circ_359866,RMVar_hsa_circ_95902,RMVar_hsa_circ_114660,RMVar_hsa_circ_147489,RMVar_hsa_circ_147490,RMVar_hsa_circ_147491 116721 RMVar_ID_116721 Human_SNP_ID_811455603 m1A Human chr11 + 57476867 57476867 57476867 CCCGAGGCCCTGCGCTCTCGGCCGGGCTCCCCAGCCCTCTGCTTTGCCTCCTGCTCCTGGTGCCC CCCGAGGCCCTGCGCTCTCGGCCGGGCTCCCCCGCCCTCTGCTTTGCCTCCTGCTCCTGGTGCCC A C RTN4RL2 Ensembl:ENSG00000186907 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57476818..57477106 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_4184046 116722 RMVar_ID_116722 Human_SNP_ID_811456966 m1A Human chr11 + 65645091 65645091 65645091 TCTCACCTTGCTGGGCGATGTGGTGCGGCTCAAAGGCTTTGAGAGTTACCGGGCCCAGCTAGACA TCTCACCTTGCTGGGCGATGTGGTGCGGCTCATAGGCTTTGAGAGTTACCGGGCCCAGCTAGACA A T SIPA1 Ensembl:ENSG00000213445 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65642284..65645862 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_1259655,Human_Splice_Rec_1259691,Human_Splice_Rec_1259723 RMVar_hsa_circ_33978,RMVar_hsa_circ_120674,RMVar_hsa_circ_150768 116723 RMVar_ID_116723 Human_SNP_ID_811472612 m1A Human chr11 - 67608446 67608446 67608446 CTCCAGTCATGGCGGCCGTACAGGTTGGTGAAAATCCGGTCTTCATCCTTCAGCGAGCCAAATGA CTCCAGTCATGGCGGCCGTACAGGTTGGTGAACATCCGGTCTTCATCCTTCAGCGAGCCAAATGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67608326..67608650 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 116724 RMVar_ID_116724 Human_SNP_ID_811473890 m1A Human chr11 + 68032330 68032330 68032330 GCCGGAGCCTCCACAGCAGTGCAGTGGCAGCCACCTACAGTGAGTACCTGGGTGGCCTCTAGCCT GCCGGAGCCTCCACAGCAGTGCAGTGGCAGCCCCCTACAGTGAGTACCTGGGTGGCCTCTAGCCT A C NDUFS8 Ensembl:ENSG00000110717 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:68032297..68032397 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_402193,Human_RBP_ID_749344,Human_RBP_ID_4185210,Human_RBP_ID_17350282 Human_Splice_Rec_1267862,Human_Splice_Rec_1267863,Human_Splice_Rec_1267874,Human_Splice_Rec_1267875,Human_Splice_Rec_1267882,Human_Splice_Rec_1267883,Human_Splice_Rec_1267892,Human_Splice_Rec_1267904,Human_Splice_Rec_1267908,Human_Splice_Rec_1267909,Human_Splice_Rec_1267916,Human_Splice_Rec_1267917,Human_Splice_Rec_1267932,Human_Splice_Rec_1267933,Human_Splice_Rec_1267938 RMVar_hsa_circ_15030,RMVar_hsa_circ_79704,RMVar_hsa_circ_122932,RMVar_hsa_circ_151101,RMVar_hsa_circ_301321,RMVar_hsa_circ_151102,RMVar_hsa_circ_151103 116725 RMVar_ID_116725 Human_SNP_ID_811486768 m1A Human chr11 + 33736319 33736319 33736319 GGGTAGCCCCCACAGACCCTCCGCCCGGGCCCAGACTGCCGCCGCCACCTCGGCTCGGCTCACCC GGGTAGCCCCCACAGACCCTCCGCCCGGGCCCCGACTGCCGCCGCCACCTCGGCTCGGCTCACCC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA heat shock 4h chr11:33736315..33736425;chr11:33736306..33736425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116726 RMVar_ID_116726 Human_SNP_ID_811495939 m1A Human chr11 - 68685640 68685640 68685640 GAGGCCATGCTGTCAGTCACTTACGTGGGCCCAGCAGGTAGCCCGCGCTGTTCAGGGTCCAGCCT GAGGCCATGCTGTCAGTCACTTACGTGGGCCCGGCAGGTAGCCCGCGCTGTTCAGGGTCCAGCCT T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:68685001..68688053 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver 116727 RMVar_ID_116727 Human_SNP_ID_811496507 m1A Human chr11 - 65506176 65506172 65506177 AAGAGTCCTGAAGACAGATTAGTAGTCAAAGCAAAGACGCCGCAGGGATTTGAACCCCGTCCTGG AAGAGTCCTGAAGACAGATTAGTAGTCAAAG_____ACGCCGCAGGGATTTGAACCCCGTCCTGG TCTTTG T TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:65506126..65506225 26863196 MeRIP-seq:(Medium) rs1250718881 Functional Loss DEL TCGA 32..36 33 SARC 1 - 116728 RMVar_ID_116728 Human_SNP_ID_811502011 m1A Human chr11 - 119335025 119335025 119335025 TCAATATTTTAGGGGGTCTGGGATTAATTTGGAAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA TCAATATTTTAGGGGGTCTGGGATTAATTTGGGAGGAAAATGAGCAGTCTCCAACCCAGGGGGTA T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:119334976..119335085 26863196 MeRIP-seq:(Medium) rs12797083 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA,large_intestine adenocarcinoma 3 stomach,large intestine GWAS_ID_11580,GWAS_ID_11581,GWAS_ID_11582,GWAS_ID_11583,GWAS_ID_11584,GWAS_ID_11585,GWAS_ID_11586,GWAS_ID_11587,GWAS_ID_11588 116729 RMVar_ID_116729 Human_SNP_ID_811522116 m1A Human chr11 + 4095105 4095105 4095105 TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGACCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT TGCGGGCTGCCGCCGCCGGAGCTGATGCCCAGCCCGCCCGCCCGCCTTCGCTGCTTCCCGCCTTT A C RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:4095080..4095300 26863196 MeRIP-seq:(Medium) rs12801088 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,oesophagus squamous_cell_carcinoma,large_intestine adenocarcinoma 7 oesophagus,large intestine RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 116730 RMVar_ID_116730 Human_SNP_ID_811535819 m1A Human chr11 - 64224651 64224651 64224651 CGCAGGCCCTGCCCCCGATGCTAGTCCATGGTACATTCTGGAAGCACTGGCCATCCATCCTACTC CGCAGGCCCTGCCCCCGATGCTAGTCCATGGTGCATTCTGGAAGCACTGGCCATCCATCCTACTC T C TRPT1 Ensembl:ENSG00000149743 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:64224602..64224701 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 GBM 2 - Human_RBP_ID_26803719 Human_Splice_Rec_1252684,Human_Splice_Rec_1252696,Human_Splice_Rec_1252706,Human_Splice_Rec_1252718,Human_Splice_Rec_1252732,Human_Splice_Rec_1252742,Human_Splice_Rec_1252766,Human_Splice_Rec_1252774,Human_Splice_Rec_1252784,Human_Splice_Rec_1252790 Human_miRNA_ID_2843408 RMVar_hsa_circ_85785,RMVar_hsa_circ_96656,RMVar_hsa_circ_150435,RMVar_hsa_circ_375890,RMVar_hsa_circ_150436,RMVar_hsa_circ_150437 116731 RMVar_ID_116731 Human_SNP_ID_811545091 m1A Human chr11 - 971166 971166 971166 TCTCCCCCAGGACAAGGGCAGGCCCAAGTTCCAGTCCCTGTGCCTCCGTCCTCAAGGCTAATCCC TCTCCCCCAGGACAAGGGCAGGCCCAAGTTCCGGTCCCTGTGCCTCCGTCCTCAAGGCTAATCCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:971153..971478 26863196 MeRIP-seq:(Medium) rs7103585 Functional Loss SNV ICGC 33..33 33 LAML 1 - 116732 RMVar_ID_116732 Human_SNP_ID_811551542 m1A Human chr11 + 33161412 33161411 33161413 AAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGC AAAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGC TAA T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:33161248..33161475;chr11:33161209..33161484;chr11:33156794..33161489 26863196 MeRIP-seq:(Medium) rs1408775438 Functional Loss DEL TCGA 33..34 33 COAD 1 - 116733 RMVar_ID_116733 Human_SNP_ID_811582208 m1A Human chr11 - 47744152 47744152 47744152 TAATTGTCATGTTCTTTGTAGGCAGAGTTGCGAGCCTTGGAGGAAGGAGATGGTAGTGTGTCAGG TAATTGTCATGTTCTTTGTAGGCAGAGTTGCGCGCCTTGGAGGAAGGAGATGGTAGTGTGTCAGG T G FNBP4 Ensembl:ENSG00000109920 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47744101..47744206 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_29740,Human_RBP_ID_292761,Human_RBP_ID_3939094,Human_RBP_ID_4162352,Human_RBP_ID_6078046,Human_RBP_ID_8229347,Human_RBP_ID_9363580,Human_RBP_ID_18468918,Human_RBP_ID_22035212,Human_RBP_ID_22736220,Human_RBP_ID_23507893,Human_RBP_ID_26317784,Human_RBP_ID_27803408 Human_Splice_Rec_1238262,Human_Splice_Rec_1238332,Human_Splice_Rec_1238346 RMVar_hsa_circ_5588,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_360503,RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_44057,RMVar_hsa_circ_79080,RMVar_hsa_circ_149626,RMVar_hsa_circ_341159,RMVar_hsa_circ_280985,RMVar_hsa_circ_275399,RMVar_hsa_circ_347418,RMVar_hsa_circ_149628,RMVar_hsa_circ_149630,RMVar_hsa_circ_287,RMVar_hsa_circ_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_71587,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_365697,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354019,RMVar_hsa_circ_354843,RMVar_hsa_circ_297666,RMVar_hsa_circ_267069,RMVar_hsa_circ_350437,RMVar_hsa_circ_149639,RMVar_hsa_circ_359423,RMVar_hsa_circ_329619,RMVar_hsa_circ_68679,RMVar_hsa_circ_149640,RMVar_hsa_circ_149641,RMVar_hsa_circ_149642 116734 RMVar_ID_116734 Human_SNP_ID_811582739 m1A Human chr11 + 75571905 75571905 75571905 CAGCGTGTTCCACGCCACCGCCTTTGAGTTGGACACAGATGGCAACCCCTTTGACCAGGACATCT CAGCGTGTTCCACGCCACCGCCTTTGAGTTGGGCACAGATGGCAACCCCTTTGACCAGGACATCT A G SERPINH1 Ensembl:ENSG00000149257 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75571854..75571958 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1782666,Human_RBP_ID_6095344,Human_RBP_ID_18188378,Human_RBP_ID_18433211,Human_RBP_ID_22435578,Human_RBP_ID_22753763 116735 RMVar_ID_116735 Human_SNP_ID_811602784 m1A Human chr11 + 64246611 64246611 64246611 CTCTGAAAGTAGACGCGTGGTCCTGGGCCGCCACTGCCCGGCCCGGGGGCCGGGGCCGCCAACGC CTCTGAAAGTAGACGCGTGGTCCTGGGCCGCCGCTGCCCGGCCCGGGGGCCGGGGCCGCCAACGC A G PPP1R14B-AS1 Ensembl:ENSG00000256940 lincRNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:64246426..64246892 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116736 RMVar_ID_116736 Human_SNP_ID_811604693 m1A Human chr11 - 57310381 57310381 57310381 CCCAGGTCTCGGAGAGAGGGACTGGACCAGCAAGTATGGGCAAGGAGCAGGGGAAGGGAGCACCA CCCAGGTCTCGGAGAGAGGGACTGGACCAGCACGTATGGGCAAGGAGCAGGGGAAGGGAGCACCA T G TNKS1BP1 Ensembl:ENSG00000149115 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:57310330..57310531 32194978 MeRIP-seq:(Medium) rs150510361 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_6078787,Human_RBP_ID_27412093 Human_miRNA_ID_1092537 116737 RMVar_ID_116737 Human_SNP_ID_811604879 m1A Human chr11 + 65018425 65018425 65018425 TCCTGAAGAAGTTCAATGGGGAGGACATCGACACCATCTCCCCAACGCTGGGCTTCAACATCAAG TCCTGAAGAAGTTCAATGGGGAGGACATCGACGCCATCTCCCCAACGCTGGGCTTCAACATCAAG A G ARL2,ARL2-SNX15 Ensembl:ENSG00000213465,Ensembl:ENSG00000273003 Protein coding,Protein coding CDS,CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65018376..65018475 32194978 MeRIP-seq:(Medium) rs780868896 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 3 lung Human_RBP_ID_400185,Human_RBP_ID_4185060,Human_RBP_ID_5110854,Human_RBP_ID_17649687,Human_RBP_ID_17798876,Human_RBP_ID_26803758 Human_Splice_Rec_1256184,Human_Splice_Rec_1256185,Human_Splice_Rec_1256192,Human_Splice_Rec_1256193,Human_Splice_Rec_1256196,Human_Splice_Rec_1256197,Human_Splice_Rec_1256206,Human_Splice_Rec_1256207,Human_Splice_Rec_1256214,Human_Splice_Rec_1256215 Human_miRNA_ID_2367250,Human_miRNA_ID_3015049 RMVar_hsa_circ_150542,RMVar_hsa_circ_119843 116738 RMVar_ID_116738 Human_SNP_ID_811613877 m1A Human chr11 + 2902359 2902359 2902359 ACCGGCACCCGTGCCCAAGCCCGCCCCTGCAAAGGCAGGTACTCGAGCACACTCCGGAGAGGGCG ACCGGCACCCGTGCCCAAGCCCGCCCCTGCAACGGCAGGTACTCGAGCACACTCCGGAGAGGGCG A C SLC22A18 Ensembl:ENSG00000110628 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2902308..2902408 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 5 kidney Human_RBP_ID_4184599 Human_Splice_Rec_1200111,Human_Splice_Rec_1200131 116739 RMVar_ID_116739 Human_SNP_ID_811617102 m1A Human chr11 + 65506345 65506345 65506345 TTGTCAGGAGCTTGACTTGATTGTATATTCATATTTACACGAGAACCTAATATAACTGCCTTGTC TTGTCAGGAGCTTGACTTGATTGTATATTCATGTTTACACGAGAACCTAATATAACTGCCTTGTC A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:65506248..65506375 26863410 MeRIP-seq:(Medium) rs1468762536 Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_RBP_ID_2295878,Human_RBP_ID_23515242 Human_Splice_Rec_1258550 116740 RMVar_ID_116740 Human_SNP_ID_811618103 m1A Human chr11 + 406949 406949 406949 CGGGGTCGCGCCTCTGGCCCTCGAAGGTGATGAAGATGGGTCTGCGGGTGAGCTCCAGCAGCCGG CGGGGTCGCGCCTCTGGCCCTCGAAGGTGATGTAGATGGGTCTGCGGGTGAGCTCCAGCAGCCGG A T - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:406838..407125 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - 116741 RMVar_ID_116741 Human_SNP_ID_811664666 m1A Human chr11 + 85484110 85484110 85484110 GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTACAAGAGGGCGTGAAACCGTTAAGAGGTAAATG GGGAAAGTTGAAAAGAACTTTGAAGAGAGAGTTCAAGAGGGCGTGAAACCGTTAAGAGGTAAATG A T - - Other Unknown GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1782892,GSM1782893 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,total RNA rearranged at 50c chr11:85483923..85484138 31548705,26863196 m1A-IP-seq:(High) rs4943920 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III,central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 2 brain Human_RBP_ID_269370,Human_RBP_ID_274754,Human_RBP_ID_407541,Human_RBP_ID_988597,Human_RBP_ID_1080809,Human_RBP_ID_1126314,Human_RBP_ID_1163695,Human_RBP_ID_1266479,Human_RBP_ID_1355340,Human_RBP_ID_1460789,Human_RBP_ID_1783212,Human_RBP_ID_2288750,Human_RBP_ID_3381471,Human_RBP_ID_4180757,Human_RBP_ID_5165775,Human_RBP_ID_5273771,Human_RBP_ID_5416414,Human_RBP_ID_5436994,Human_RBP_ID_5460919,Human_RBP_ID_5490486,Human_RBP_ID_5550310,Human_RBP_ID_6099833,Human_RBP_ID_8065206,Human_RBP_ID_8246589,Human_RBP_ID_8360232,Human_RBP_ID_8772194,Human_RBP_ID_9007448,Human_RBP_ID_9275194,Human_RBP_ID_9649802,Human_RBP_ID_10482337,Human_RBP_ID_11732219,Human_RBP_ID_16988134,Human_RBP_ID_17062361,Human_RBP_ID_17067119,Human_RBP_ID_17108855,Human_RBP_ID_17184918,Human_RBP_ID_17233287,Human_RBP_ID_17349546,Human_RBP_ID_17466351,Human_RBP_ID_17682743,Human_RBP_ID_17806510,Human_RBP_ID_18176556,Human_RBP_ID_18198780,Human_RBP_ID_18205933,Human_RBP_ID_18252749,Human_RBP_ID_18433266,Human_RBP_ID_18510800,Human_RBP_ID_18526386,Human_RBP_ID_18613774,Human_RBP_ID_19583612,Human_RBP_ID_21916183,Human_RBP_ID_22167734,Human_RBP_ID_22381455,Human_RBP_ID_22420775,Human_RBP_ID_22491904,Human_RBP_ID_22792370,Human_RBP_ID_22894258,Human_RBP_ID_23124855,Human_RBP_ID_23155198,Human_RBP_ID_23267411,Human_RBP_ID_23305516,Human_RBP_ID_23524281,Human_RBP_ID_24404522,Human_RBP_ID_24462450,Human_RBP_ID_24905710,Human_RBP_ID_26407604,Human_RBP_ID_26606351,Human_RBP_ID_26747738,Human_RBP_ID_26898389,Human_RBP_ID_27154505,Human_RBP_ID_27208771,Human_RBP_ID_27416609,Human_RBP_ID_27620106 116742 RMVar_ID_116742 Human_SNP_ID_811667414 m1A Human chr11 + 65443241 65443226 65443242 GGCTCAGCAGTCTGCTCCATGTGTTTTGATGCAGGGTGACCCATTGGTATTCCCGACACTAACGC GGCTCAGCAGTCTGCTCC________________GGTGACCCATTGGTATTCCCGACACTAACGC CATGTGTTTTGATGCAG C NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65443193..65443272 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 19..34 33 ESCA 1 - Human_RBP_ID_400641,Human_RBP_ID_806392,Human_RBP_ID_1080415,Human_RBP_ID_1162882,Human_RBP_ID_1265319,Human_RBP_ID_1459090,Human_RBP_ID_1781414,Human_RBP_ID_2275952,Human_RBP_ID_5093149,Human_RBP_ID_5550981,Human_RBP_ID_8064369,Human_RBP_ID_8355677,Human_RBP_ID_9005323,Human_RBP_ID_9644738,Human_RBP_ID_11673205,Human_RBP_ID_17108649,Human_RBP_ID_18478600,Human_RBP_ID_18610761,Human_RBP_ID_19582916,Human_RBP_ID_22381180,Human_RBP_ID_22791540,Human_RBP_ID_22896600,Human_RBP_ID_23514363,Human_RBP_ID_24404048,Human_RBP_ID_24461679,Human_RBP_ID_24896802,Human_RBP_ID_26768221,Human_RBP_ID_26894504 RMVar_hsa_circ_113760,RMVar_hsa_circ_150643 116743 RMVar_ID_116743 Human_SNP_ID_811674978 m1A Human chr11 + 72237225 72237218 72237226 CCCTGCCTACTACGTCCTTGAAGGGGTCCCGCACCAGCTGCTGCCCCCGGAGCCACCCTCGCCTG CCCTGCCTACTACGTCCTTGAAGGGG________CAGCTGCTGCCCCCGGAGCCACCCTCGCCTG GTCCCGCAC G INPPL1 Ensembl:ENSG00000165458 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72237176..72237298 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 27..34 33 PRAD 1 - Human_RBP_ID_226833,Human_RBP_ID_3939698,Human_RBP_ID_5110952 Human_miRNA_ID_2051776 RMVar_hsa_circ_95334,RMVar_hsa_circ_151526 116744 RMVar_ID_116744 Human_SNP_ID_811681533 m1A Human chr11 + 61964782 61964782 61964782 CCAGGGTGTGCTTGTCAAAGAGATATTCCGCCAAGCCAGATTCGGGCGCTCCCATCTTGCGCAAG CCAGGGTGTGCTTGTCAAAGAGATATTCCGCCTAGCCAGATTCGGGCGCTCCCATCTTGCGCAAG A T BEST1 Ensembl:ENSG00000167995 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:61964673..61964824;chr11:61964690..61964809;chr11:61964678..61964818;chr11:61964678..61964816 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 7 lung 116745 RMVar_ID_116745 Human_SNP_ID_811713615 m1A Human chr11 + 68436955 68436955 68436955 CGGCCAGTGTGTCCTCATCAAACAGCAGTGCGACTCCTTCCCCGACTGTATCGACGGCTCCGACG CGGCCAGTGTGTCCTCATCAAACAGCAGTGCGCCTCCTTCCCCGACTGTATCGACGGCTCCGACG A C LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68436904..68437040 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_Splice_Rec_1268540,Human_Splice_Rec_1268541,Human_Splice_Rec_1268582,Human_Splice_Rec_1268583 RMVar_hsa_circ_2374,RMVar_hsa_circ_81769,RMVar_hsa_circ_151161,RMVar_hsa_circ_124136,RMVar_hsa_circ_151174,RMVar_hsa_circ_122875,RMVar_hsa_circ_151178,RMVar_hsa_circ_371280,RMVar_hsa_circ_151189,RMVar_hsa_circ_151188,RMVar_hsa_circ_101643,RMVar_hsa_circ_80814,RMVar_hsa_circ_151197,RMVar_hsa_circ_67213,RMVar_hsa_circ_151205 116746 RMVar_ID_116746 Human_SNP_ID_811728176 m1A Human chr11 - 2929316 2929316 2929316 AGGTGCTACGCGAGGGCGAGTTGGAGAAGCGCAGCGACAGCCTCTTCCAGCTATGGAAGAAGAAG AGGTGCTACGCGAGGGCGAGTTGGAGAAGCGCGGCGACAGCCTCTTCCAGCTATGGAAGAAGAAG T C PHLDA2 Ensembl:ENSG00000181649 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:2929215..2929360 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116747 RMVar_ID_116747 Human_SNP_ID_811737595 m1A Human chr11 + 64765947 64765947 64765947 TCCATGGGAGGCGGAGGAGGAGGGGGCGGGGCATACATCATGCCGGCGGAACCAGGCGGTGGAGG TCCATGGGAGGCGGAGGAGGAGGGGGCGGGGCCTACATCATGCCGGCGGAACCAGGCGGTGGAGG A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64765942..64766056 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 8 head and neck 116748 RMVar_ID_116748 Human_SNP_ID_811740588 m1A Human chr11 + 65885581 65885581 65885581 GTTTTGGATCATGAGCTCAGCGCAGAAGGCAAAGTCACCGAAGCTCAGATACTGCAGTTTTTTCT GTTTTGGATCATGAGCTCAGCGCAGAAGGCAATGTCACCGAAGCTCAGATACTGCAGTTTTTTCT A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:65885493..65885650;chr11:65885496..65885580 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine 116749 RMVar_ID_116749 Human_SNP_ID_811753713 m1A Human chr11 - 61132229 61132229 61132229 ATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCATGGAGCCCTGCCACCGGCCCCTTTCCCAGTAG ATCCCCCAGCCTGCCTGTGGGCCCCACTGCCCGTGGAGCCCTGCCACCGGCCCCTTTCCCAGTAG T C VPS37C Ensembl:ENSG00000167987 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:61132182..61132384 26863196 MeRIP-seq:(Medium) rs2232143 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma,lung large_cell_carcinoma,lung non_small_cell_carcinoma 3 lung Human_RBP_ID_5126573,Human_RBP_ID_5234993,Human_RBP_ID_17073686 RMVar_hsa_circ_82976,RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149901,RMVar_hsa_circ_149902 116750 RMVar_ID_116750 Human_SNP_ID_811760671 m1A Human chr11 + 8964381 8964381 8964381 CCGCGACCGGCTCCCGGCTCGGGCTCAGGCTCAGGCTCAGGCTCAGGCACAGGCTTGGGACCCGG CCGCGACCGGCTCCCGGCTCGGGCTCAGGCTCGGGCTCAGGCTCAGGCACAGGCTTGGGACCCGG A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8964274..8964382 26863196 MeRIP-seq:(Medium) rs1009700001 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COCA,UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 10 uterus,large intestine 116751 RMVar_ID_116751 Human_SNP_ID_811764614 m1A Human chr11 + 412727 412725 412728 TGCCCAGCTCTAACCATGTCTGGATGCAGTCGAGGGGGGGTGCCCAGCTCTGGCCCACGTCTGGT TGCCCAGCTCTAACCATGTCTGGATGCAGTC___GGGGGGTGCCCAGCTCTGGCCCACGTCTGGT CGAG C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:412721..412805 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 CHOL 1 - 116752 RMVar_ID_116752 Human_SNP_ID_811766708 m1A Human chr11 + 65341038 65341038 65341038 CTGGCGGAAAAAGCGGCGAGCCCATCCCCCTGAGGATCCACGACTTTCCTTCCCATCTATTAAGC CTGGCGGAAAAAGCGGCGAGCCCATCCCCCTGTGGATCCACGACTTTCCTTCCCATCTATTAAGC A T DPF2 Ensembl:ENSG00000133884 Protein coding exon GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65341001..65341050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_22433107 Human_Splice_Rec_1258146,Human_Splice_Rec_1258147,Human_Splice_Rec_1258152,Human_Splice_Rec_1258153,Human_Splice_Rec_1258172,Human_Splice_Rec_1258173,Human_Splice_Rec_1258180,Human_Splice_Rec_1258181,Human_Splice_Rec_1258194,Human_Splice_Rec_1258195,Human_Splice_Rec_1258214,Human_Splice_Rec_1258215,Human_Splice_Rec_1258226,Human_Splice_Rec_1258227,Human_Splice_Rec_1258240,Human_Splice_Rec_1258241 Human_miRNA_ID_1970712 RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_317447,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627 116753 RMVar_ID_116753 Human_SNP_ID_811779207 m1A Human chr11 - 1017735 1017735 1017735 CAGCCAAGCCCTGAGCTCATTAAACACAGCCAAAACCTCTACATCCCTACATTCACACACTTCCT CAGCCAAGCCCTGAGCTCATTAAACACAGCCACAACCTCTACATCCCTACATTCACACACTTCCT T G MUC6 Ensembl:ENSG00000184956 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:1017684..1017835 26863196 MeRIP-seq:(Medium) rs1309107982 Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - 116754 RMVar_ID_116754 Human_SNP_ID_811779498 m1A Human chr11 + 65965210 65965210 65965210 GCGGCTGCCAAGGAGAAGCGCCTGCTGAACCAAAAGCTGGGGTGAGGGGTCCTGGCCAGGGCAGG GCGGCTGCCAAGGAGAAGCGCCTGCTGAACCAGAAGCTGGGGTGAGGGGTCCTGGCCAGGGCAGG A G SART1 Ensembl:ENSG00000175467 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65965076..65965251 26863196 MeRIP-seq:(Medium) rs866857445 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_17804656,Human_RBP_ID_18974219 Human_Splice_Rec_1261251,Human_Splice_Rec_1261273,Human_Splice_Rec_1261281 Human_miRNA_ID_2359808 RMVar_hsa_circ_150811,RMVar_hsa_circ_119726,RMVar_hsa_circ_265184 116755 RMVar_ID_116755 Human_SNP_ID_811800130 m1A Human chr11 - 830984 830984 830984 GGCGGCCTCGTGCTTCGCTCTCCAGCCTGCGGATCTGCTCCTGCGCCCCCTCCAGCTGCGTTCGC GGCGGCCTCGTGCTTCGCTCTCCAGCCTGCGGTTCTGCTCCTGCGCCCCCTCCAGCTGCGTTCGC T A AP006621.1 Ensembl:ENSG00000255108 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:830953..831038 26863196 MeRIP-seq:(Medium) rs1389667003 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 116756 RMVar_ID_116756 Human_SNP_ID_811807806 m1A Human chr11 + 86302319 86302319 86302319 GGGGCAGAGGCATTCTTGCCGCTGGCCCAGTCACTATGTAGTGGAGGGGCAGACACCCTCCCGCA GGGGCAGAGGCATTCTTGCCGCTGGCCCAGTCGCTATGTAGTGGAGGGGCAGACACCCTCCCGCA A G HIKESHI Ensembl:ENSG00000149196 Protein coding 5'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs291241 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_405364,Human_RBP_ID_4181034,Human_RBP_ID_9321760,Human_RBP_ID_18417011,Human_RBP_ID_22435596 Human_miRNA_ID_2037328,Human_miRNA_ID_2151534,Human_miRNA_ID_2348032 GWAS_ID_8218,GWAS_ID_8219,GWAS_ID_8220,GWAS_ID_8221,GWAS_ID_8222,GWAS_ID_8223,GWAS_ID_8224 116757 RMVar_ID_116757 Human_SNP_ID_811808491 m1A Human chr11 - 66057377 66057377 66057377 TCTCTTATCCCTAGGAATAAATCATCAGTCTCACCTCTCTGTTCTCATCTCCAGGGGGCGGTGGG TCTCTTATCCCTAGGAATAAATCATCAGTCTCGCCTCTCTGTTCTCATCTCCAGGGGGCGGTGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:66057326..66057400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 116758 RMVar_ID_116758 Human_SNP_ID_811835999 m1A Human chr11 - 65590541 65590541 65590541 GCCTCCGGATGAGAGCGTTCTTCTTGTTGACCAGGGTGAACCACTCCTGGATCAGCACCTCCTCC GCCTCCGGATGAGAGCGTTCTTCTTGTTGACCGGGGTGAACCACTCCTGGATCAGCACCTCCTCC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65590467..65590577 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116759 RMVar_ID_116759 Human_SNP_ID_811836324 m1A Human chr11 - 118908652 118908652 118908652 CTTTTCACATTTCTCCCACCTCCTCCCAGGTTACCCCACCCCAGGAGGAGAGAAGCTCCAGGGAG CTTTTCACATTTCTCCCACCTCCTCCCAGGTTCCCCCACCCCAGGAGGAGAGAAGCTCCAGGGAG T G BCL9L Ensembl:ENSG00000186174 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118908465..118910023 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5126786,Human_RBP_ID_5346279 Human_Splice_Rec_1305652,Human_Splice_Rec_1305666,Human_Splice_Rec_1305692 RMVar_hsa_circ_72117 116760 RMVar_ID_116760 Human_SNP_ID_811861092 m1A Human chr11 - 123058486 123058486 123058486 TAAGGCTTTTACTTAGAGTTAATTTCTTTCCTAGGCCGTTTGAGCAAGGAAGACATTGAACGTAT TAAGGCTTTTACTTAGAGTTAATTTCTTTCCTGGGCCGTTTGAGCAAGGAAGACATTGAACGTAT T C HSPA8 Ensembl:ENSG00000109971 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:123058234..123058486 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus Human_RBP_ID_24913188 RMVar_hsa_circ_69907,RMVar_hsa_circ_97942,RMVar_hsa_circ_153774,RMVar_hsa_circ_76803,RMVar_hsa_circ_153775,RMVar_hsa_circ_375749,RMVar_hsa_circ_153777 116761 RMVar_ID_116761 Human_SNP_ID_811869446 m1A Human chr11 + 62614279 62614279 62614279 TCCCTTTGCAGCCGGATCCAGAGCAATGTAGAAGGCCTATACCTGACTGATGGGGTCCCTTTCTC TCCCTTTGCAGCCGGATCCAGAGCAATGTAGACGGCCTATACCTGACTGATGGGGTCCCTTTCTC A C ROM1 Ensembl:ENSG00000149489 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62614273..62614375 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,COCA,large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_1248266,Human_Splice_Rec_1248268,Human_Splice_Rec_1248272,Human_Splice_Rec_1248276 116762 RMVar_ID_116762 Human_SNP_ID_811874384 m1A Human chr11 + 67504186 67504182 67504187 CAGAATGTGGTATTCCTTGATGAGCATCCTGAAGGCGCTCGGCGGGCCGCGCGCGGCCTCCGCTC CAGAATGTGGTATTCCTTGATGAGCATCC_____GCGCTCGGCGGGCCGCGCGCGGCCTCCGCTC CTGAAG C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67504019..67504341 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 30..34 33 PBCA 1 - 116763 RMVar_ID_116763 Human_SNP_ID_811878322 m1A Human chr11 - 72697651 72697651 72697651 GACCTGGGCCTCACCTTGACTAACCCCTCCACAGCCATCCAGGGGGACAGTGAGAACCAGGTGCT GACCTGGGCCTCACCTTGACTAACCCCTCCACGGCCATCCAGGGGGACAGTGAGAACCAGGTGCT T C ARAP1 Ensembl:ENSG00000186635 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72696921..72700038 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 7 lung Human_RBP_ID_866092,Human_RBP_ID_5344285,Human_RBP_ID_22537760 Human_Splice_Rec_1274699,Human_Splice_Rec_1274765,Human_Splice_Rec_1274801,Human_Splice_Rec_1274861,Human_Splice_Rec_1274917,Human_Splice_Rec_1274981,Human_Splice_Rec_1275049,Human_Splice_Rec_1275113,Human_Splice_Rec_1275173,Human_Splice_Rec_1275275,Human_Splice_Rec_1275291 RMVar_hsa_circ_62676,RMVar_hsa_circ_81133,RMVar_hsa_circ_151542,RMVar_hsa_circ_151548,RMVar_hsa_circ_76563,RMVar_hsa_circ_111134,RMVar_hsa_circ_78797,RMVar_hsa_circ_151549,RMVar_hsa_circ_151550,RMVar_hsa_circ_76699,RMVar_hsa_circ_86069,RMVar_hsa_circ_151551,RMVar_hsa_circ_151552 116764 RMVar_ID_116764 Human_SNP_ID_811878643 m1A Human chr11 - 119095366 119095366 119095366 TAGCATGTCGGGCCGCGGCAAGACTGGCGGCAAGGCCCGCGCCAAGGCCAAGTCGCGCTCGTCGC TAGCATGTCGGGCCGCGGCAAGACTGGCGGCAGGGCCCGCGCCAAGGCCAAGTCGCGCTCGTCGC T C H2AX Ensembl:ENSG00000188486 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119095320..119095401 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus Human_RBP_ID_228109,Human_RBP_ID_4184450,Human_RBP_ID_5313848,Human_RBP_ID_5461197,Human_RBP_ID_9321804,Human_RBP_ID_18188389,Human_RBP_ID_22433290,Human_RBP_ID_22705606,Human_RBP_ID_22789742,Human_RBP_ID_23207125,Human_RBP_ID_26886754 116765 RMVar_ID_116765 Human_SNP_ID_811881372 m1A Human chr11 + 65716977 65716974 65716977 CCAGCGCCGGGGCTACGGCAAGCTGCTGATCGAGTTCAGTGAGTATGTGTGCTGCGGCCAGGGGG CCAGCGCCGGGGCTACGGCAAGCTGCTGAT___GTTCAGTGAGTATGTGTGCTGCGGCCAGGGGG TCGA T KAT5 Ensembl:ENSG00000172977 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65716794..65716976 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 31..33 33 LUSC 1 - Human_RBP_ID_867797,Human_RBP_ID_5341644,Human_RBP_ID_18972295,Human_RBP_ID_19052239,Human_RBP_ID_22643483 Human_Splice_Rec_1260108,Human_Splice_Rec_1260109,Human_Splice_Rec_1260132,Human_Splice_Rec_1260133,Human_Splice_Rec_1260160,Human_Splice_Rec_1260161,Human_Splice_Rec_1260196,Human_Splice_Rec_1260197,Human_Splice_Rec_1260270,Human_Splice_Rec_1260271,Human_Splice_Rec_1260290 116766 RMVar_ID_116766 Human_SNP_ID_811906170 m1A Human chr11 - 94545483 94545483 94545483 TCGTCCACGTGGATGAAGGCGCCGCGGGGCACAAAGCGCTCGTAGTTGGCACGGTCTGGGCCCAG TCGTCCACGTGGATGAAGGCGCCGCGGGGCACCAAGCGCTCGTAGTTGGCACGGTCTGGGCCCAG T G AP000943.2 Ensembl:ENSG00000255929 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:94545432..94545532 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - 116767 RMVar_ID_116767 Human_SNP_ID_811916639 m1A Human chr11 - 2390476 2390476 2390476 GCGCGGGCTTGTCTCCCAGCTCCAGATACAGGAGGTTGGTGGTCTGCGGGTCATGGCGGAGCCAC GCGCGGGCTTGTCTCCCAGCTCCAGATACAGGTGGTTGGTGGTCTGCGGGTCATGGCGGAGCCAC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:2390426..2390500 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - 116768 RMVar_ID_116768 Human_SNP_ID_811920256 m1A Human chr11 - 112086697 112086697 112086697 CGAACAATGGCGGAGCTGGGCGAAGCCGATGAAGCGGAGTTGCAGCGCCTGGTGGCCGCCGAGCA CGAACAATGGCGGAGCTGGGCGAAGCCGATGAGGCGGAGTTGCAGCGCCTGGTGGCCGCCGAGCA T C TIMM8B Ensembl:ENSG00000150779 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEK-293T cells,m1A-IP-seq;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:112086626..112086750;chr11:112086612..112086750;chr11:112086619..112086750 31548705,26863196 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,OV,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_227779,Human_RBP_ID_388975,Human_RBP_ID_751377,Human_RBP_ID_1454097,Human_RBP_ID_4184409,Human_RBP_ID_22433928 Human_Splice_Rec_1297745,Human_Splice_Rec_1297747,Human_Splice_Rec_1297751,Human_Splice_Rec_1297753 116769 RMVar_ID_116769 Human_SNP_ID_811930244 m1A Human chr11 - 27357540 27357540 27357540 TACAAGTACTATAGTAGCCTCTCTTTTGTAGCACTCAGGTTGAATCAGAAAATAACCAAGAAGAA TACAAGTACTATAGTAGCCTCTCTTTTGTAGCGCTCAGGTTGAATCAGAAAATAACCAAGAAGAA T C CCDC34 Ensembl:ENSG00000109881 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:27357357..27357587 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_9362079 Human_Splice_Rec_1222038,Human_Splice_Rec_1222048 116770 RMVar_ID_116770 Human_SNP_ID_811949982 m1A Human chr11 - 65539225 65539225 65539225 GCCGCACCTGTCGCCCTCACCTTCAGATATCGACGAGTGCCGAGAGCTGAACCAGCGCGGGCTGC GCCGCACCTGTCGCCCTCACCTTCAGATATCGTCGAGTGCCGAGAGCTGAACCAGCGCGGGCTGC T A LTBP3 Ensembl:ENSG00000168056 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:65539204..65539457 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 7 caecum,large intestine Human_RBP_ID_18159415,Human_RBP_ID_18972231,Human_RBP_ID_22434616 Human_Splice_Rec_1258908,Human_Splice_Rec_1258926,Human_Splice_Rec_1258980,Human_Splice_Rec_1259004,Human_Splice_Rec_1259026,Human_Splice_Rec_1259058,Human_Splice_Rec_1259110,Human_Splice_Rec_1259152,Human_Splice_Rec_1259162 Human_miRNA_ID_271145 116771 RMVar_ID_116771 Human_SNP_ID_811978249 m1A Human chr11 + 66700719 66700719 66700719 GGTCAGCCTGGTCCCGGGTCACCTCCTCGCCCAGGGCTCGCAGCCGGCTATACTCGCTCTGGGCC GGTCAGCCTGGTCCCGGGTCACCTCCTCGCCCGGGGCTCGCAGCCGGCTATACTCGCTCTGGGCC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66700672..66700778 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine 116772 RMVar_ID_116772 Human_SNP_ID_811995745 m1A Human chr11 - 117205992 117205992 117205992 GCACGGGAAGGAGGAGCAGATCTGCTGACCTCAGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC GCACGGGAAGGAGGAGCAGATCTGCTGACCTCGGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC T C PCSK7 Ensembl:ENSG00000160613 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35186251 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_82321,RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153290,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286 116773 RMVar_ID_116773 Human_SNP_ID_811999500 m1A Human chr11 - 549934 549934 549934 GGTCAGCGAGGCCACAGCGAGCCAGCCACAGCACCTGCAGGTGGCCCAGAGACGTGCCCAAGTCC GGTCAGCGAGGCCACAGCGAGCCAGCCACAGCGCCTGCAGGTGGCCCAGAGACGTGCCCAAGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:540827..550088 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 116774 RMVar_ID_116774 Human_SNP_ID_812000995 m1A Human chr11 - 67682754 67682754 67682754 TGCAGCATCCAGTTCATCTTAAGAATGTCAACAATTAGTCATGCAATAAATGTTCTGGTTTTAAA TGCAGCATCCAGTTCATCTTAAGAATGTCAACGATTAGTCATGCAATAAATGTTCTGGTTTTAAA T C - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879110440 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_26410684 116775 RMVar_ID_116775 Human_SNP_ID_812005820 m1A Human chr11 - 811579 811579 811579 CAGCTCACTGATAACCTGAAGCAGACAATCACAGGGCTGTTACCAGGAATGTACGATTGTATCCC CAGCTCACTGATAACCTGAAGCAGACAATCACGGGGCTGTTACCAGGAATGTACGATTGTATCCC T C - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,ALKBH3 KO;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr11:811576..811650;chr11:811576..811700 26863196,26863410,26863196,26863196,26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - 116776 RMVar_ID_116776 Human_SNP_ID_812012358 m1A Human chr11 - 61299977 61299977 61299977 CAGTTCCCCTATGTGGAAGTGGGGCGGGCTTCATAGAGACTTGGGAATGAGCTGAAGGTGAAACA CAGTTCCCCTATGTGGAAGTGGGGCGGGCTTCTTAGAGACTTGGGAATGAGCTGAAGGTGAAACA T A DDB1 Ensembl:ENSG00000167986 Protein coding 3'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:61299901..61300000 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_31311,Human_RBP_ID_398281,Human_RBP_ID_4164663,Human_RBP_ID_8774105,Human_RBP_ID_9275599,Human_RBP_ID_11651216,Human_RBP_ID_17648414,Human_RBP_ID_17797685,Human_RBP_ID_23510108 RMVar_hsa_circ_90525,RMVar_hsa_circ_109208,RMVar_hsa_circ_113892,RMVar_hsa_circ_116468,RMVar_hsa_circ_94302,RMVar_hsa_circ_106151,RMVar_hsa_circ_91994,RMVar_hsa_circ_149933,RMVar_hsa_circ_149937,RMVar_hsa_circ_149939,RMVar_hsa_circ_81659,RMVar_hsa_circ_149940,RMVar_hsa_circ_149938,RMVar_hsa_circ_149935,RMVar_hsa_circ_149936,RMVar_hsa_circ_149934 116777 RMVar_ID_116777 Human_SNP_ID_812021356 m1A Human chr11 - 62888566 62888566 62888566 GGGTGCTGAGCAGGAGGTCAGCCTTGGCTGGCAGGCTGGCGCTGGCAGGCAGGTCGGAGGCCTGC GGGTGCTGAGCAGGAGGTCAGCCTTGGCTGGCTGGCTGGCGCTGGCAGGCAGGTCGGAGGCCTGC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:62888517..62888678 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116778 RMVar_ID_116778 Human_SNP_ID_812029888 m1A Human chr11 + 62601578 62601578 62601578 CCGCTTCGAGGGAGTCTCACTGGGGCCCGCGCAGCCGGCACCTCCGCTGCCTCAGCCGTCGCGGT CCGCTTCGAGGGAGTCTCACTGGGGCCCGCGCGGCCGGCACCTCCGCTGCCTCAGCCGTCGCGGT A G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:62601396..62601850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116779 RMVar_ID_116779 Human_SNP_ID_812030958 m1A Human chr11 - 64010138 64010138 64010138 ACACCCCAGGCAACACTTCAACCAACACCCCAACCAACCCCCCAACCAACACCCCAGCCAACCCC ACACCCCAGGCAACACTTCAACCAACACCCCAGCCAACCCCCCAACCAACACCCCAGCCAACCCC T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:64010128..64010249 26863196 MeRIP-seq:(Medium) rs867110388 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,oesophagus adenocarcinoma,PEME 7 oesophagus,prostate Human_RBP_ID_193366 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_150397 116780 RMVar_ID_116780 Human_SNP_ID_812033705 m1A Human chr11 + 119336173 119336173 119336173 AGGAGGCCAGGACCATCAGAGTGACACCTGTCAGGGGCCGAGAGAGGCTCAATGAGGAGGAGCCT AGGAGGCCAGGACCATCAGAGTGACACCTGTCGGGGGCCGAGAGAGGCTCAATGAGGAGGAGCCT A G RNF26 Ensembl:ENSG00000173456 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:119336126..119336255 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 116781 RMVar_ID_116781 Human_SNP_ID_812062380 m1A Human chr11 - 35975694 35975694 35975694 TCTGTCCTACAAAGCTCAGTACCAAAGATTACACCAGTTGCACTCCAGTGCCTATACTGTTTGTT TCTGTCCTACAAAGCTCAGTACCAAAGATTACGCCAGTTGCACTCCAGTGCCTATACTGTTTGTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:35975688..35975799 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116782 RMVar_ID_116782 Human_SNP_ID_812067282 m1A Human chr11 + 4082294 4082294 4082294 TGGCTGCAGCTGACACATGAGGTGGAGGTGCAATATTACAACATCAAGAAGCAAAATGCTGAGAA TGGCTGCAGCTGACACATGAGGTGGAGGTGCAGTATTACAACATCAAGAAGCAAAATGCTGAGAA A G STIM1 Ensembl:ENSG00000167323 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:4082244..4082347 26863196 MeRIP-seq:(Medium) rs2304891 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_987082,Human_RBP_ID_17795822 Human_Splice_Rec_1202405,Human_Splice_Rec_1202427,Human_Splice_Rec_1202449,Human_Splice_Rec_1202541,Human_Splice_Rec_1202551,Human_Splice_Rec_1202561 GWAS_ID_6819,GWAS_ID_6820,GWAS_ID_6821 RMVar_hsa_circ_104299,RMVar_hsa_circ_147736,RMVar_hsa_circ_84531,RMVar_hsa_circ_147747,RMVar_hsa_circ_119467,RMVar_hsa_circ_308319,RMVar_hsa_circ_99657,RMVar_hsa_circ_43338,RMVar_hsa_circ_147746,RMVar_hsa_circ_308029,RMVar_hsa_circ_147754,RMVar_hsa_circ_147755,RMVar_hsa_circ_340651,RMVar_hsa_circ_147759,RMVar_hsa_circ_80919,RMVar_hsa_circ_147758 116783 RMVar_ID_116783 Human_SNP_ID_812070696 m1A Human chr11 - 57328361 57328361 57328361 TAATGAGGGTGACAGTGACCGGGATGAGAAGAAGCGGAAACAGCTCAAAAAGGCCAAGATGGCCA TAATGAGGGTGACAGTGACCGGGATGAGAAGATGCGGAAACAGCTCAAAAAGGCCAAGATGGCCA T A SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57328257..57328440 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_RBP_ID_870815,Human_RBP_ID_1457481,Human_RBP_ID_1779916,Human_RBP_ID_3376205,Human_RBP_ID_4190991,Human_RBP_ID_6078812,Human_RBP_ID_8352827,Human_RBP_ID_9275565,Human_RBP_ID_9362243,Human_RBP_ID_11642269,Human_RBP_ID_17465015,Human_RBP_ID_18410593,Human_RBP_ID_24542335,Human_RBP_ID_26317786,Human_RBP_ID_26804626,Human_RBP_ID_27804449 Human_Splice_Rec_1239505,Human_Splice_Rec_1239534,Human_Splice_Rec_1239535,Human_Splice_Rec_1239550,Human_Splice_Rec_1239551 RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_94097,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_78264,RMVar_hsa_circ_101451,RMVar_hsa_circ_111815,RMVar_hsa_circ_149746,RMVar_hsa_circ_79048,RMVar_hsa_circ_149748,RMVar_hsa_circ_149750,RMVar_hsa_circ_149749,RMVar_hsa_circ_44300,RMVar_hsa_circ_149747 116784 RMVar_ID_116784 Human_SNP_ID_812076359 m1A Human chr11 - 72007355 72007355 72007355 AGCCTCACCTATCTCCCAGCGCCTGCCCCCCAAGGTAGAATCCCTGGAGAGTCTCTACTTCACTC AGCCTCACCTATCTCCCAGCGCCTGCCCCCCACGGTAGAATCCCTGGAGAGTCTCTACTTCACTC T G NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:72007312..72007380 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate Human_RBP_ID_8773835,Human_RBP_ID_9364054 Human_Splice_Rec_1272218,Human_Splice_Rec_1272266,Human_Splice_Rec_1272318,Human_Splice_Rec_1272370,Human_Splice_Rec_1272416,Human_Splice_Rec_1272464,Human_Splice_Rec_1272510,Human_Splice_Rec_1272524 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_61487 116785 RMVar_ID_116785 Human_SNP_ID_812077076 m1A Human chr11 + 71444067 71444067 71444067 CGTTATAGGTGGAGTCTTGGCCCAGATGTCCGAGAGCCGAGCATGTCCGGTGACGATGTCCACCA CGTTATAGGTGGAGTCTTGGCCCAGATGTCCGCGAGCCGAGCATGTCCGGTGACGATGTCCACCA A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:71443976..71444175 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 116786 RMVar_ID_116786 Human_SNP_ID_812086479 m1A Human chr11 - 6456684 6456684 6456684 TGGGCCAGCCTGCCTCGCTCACTGTCACTACCAAAGACAAGGACGGGCGGTTGGTGCGCACAGGC TGGGCCAGCCTGCCTCGCTCACTGTCACTACCCAAGACAAGGACGGGCGGTTGGTGCGCACAGGC T G TRIM3 Ensembl:ENSG00000110171 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6456633..6456981 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung RMVar_hsa_circ_44152 116787 RMVar_ID_116787 Human_SNP_ID_812111660 m1A Human chr11 - 134220670 134220670 134220670 TGGATTTCACAGAGACTGAGCCTTTGGATCCCAGCATAGAAGCAGAGATCATAGAGACTGGATTG TGGATTTCACAGAGACTGAGCCTTTGGATCCCTGCATAGAAGCAGAGATCATAGAGACTGGATTG T A NCAPD3 Ensembl:ENSG00000151503 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:134220626..134220783 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_1455256,Human_RBP_ID_1777044,Human_RBP_ID_2259488,Human_RBP_ID_4185499,Human_RBP_ID_5461201,Human_RBP_ID_6056915,Human_RBP_ID_9363173,Human_RBP_ID_11566682,Human_RBP_ID_18605179 Human_Splice_Rec_1318542,Human_Splice_Rec_1318543,Human_Splice_Rec_1318608,Human_Splice_Rec_1318609,Human_Splice_Rec_1318674,Human_Splice_Rec_1318675,Human_Splice_Rec_1318760,Human_Splice_Rec_1318761,Human_Splice_Rec_1318776,Human_Splice_Rec_1318780 RMVar_hsa_circ_378746,RMVar_hsa_circ_18625 116788 RMVar_ID_116788 Human_SNP_ID_812143969 m1A Human chr11 - 47179502 47179502 47179502 GCTACATGGAGGACATGGAACAGGCCTTTGAGACCTGCCAGGCCGCCGAGCGCCAGCGGCTTCTT GCTACATGGAGGACATGGAACAGGCCTTTGAGCCCTGCCAGGCCGCCGAGCGCCAGCGGCTTCTT T G PACSIN3 Ensembl:ENSG00000165912 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:47179451..47179538 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_1235450,Human_Splice_Rec_1235451,Human_Splice_Rec_1235468,Human_Splice_Rec_1235469,Human_Splice_Rec_1235486,Human_Splice_Rec_1235487,Human_Splice_Rec_1235508,Human_Splice_Rec_1235509,Human_Splice_Rec_1235524,Human_Splice_Rec_1235525,Human_Splice_Rec_1235536 RMVar_hsa_circ_15209,RMVar_hsa_circ_80682,RMVar_hsa_circ_112915,RMVar_hsa_circ_149490,RMVar_hsa_circ_149492,RMVar_hsa_circ_76795,RMVar_hsa_circ_149491 116789 RMVar_ID_116789 Human_SNP_ID_812144024 m1A Human chr11 - 66371694 66371682 66371694 CGACTCCAGCCGCCCTGCACCGGAATCTGGGGAGACCCGCCCCCCGCCCCACCGGTCTGCGGCCC CGACTCCAGCCGCCCTGCACCGGAATCTGGGG____________CGCCCCACCGGTCTGCGGCCC GGGGGGCGGGTCT G SLC29A2 Ensembl:ENSG00000174669 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:66371626..66371717 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..44 33 PAAD 1 - Human_RBP_ID_401440,Human_RBP_ID_4185146 116790 RMVar_ID_116790 Human_SNP_ID_812154837 m1A Human chr11 + 65182793 65182793 65182793 GCAGCGGGCCAGGGAGCTGGGCCTGGGCCGCCATGAGAATGCCATCAAGTACCTGGGCCAGGATT GCAGCGGGCCAGGGAGCTGGGCCTGGGCCGCCGTGAGAATGCCATCAAGTACCTGGGCCAGGATT A G CAPN1 Ensembl:ENSG00000014216 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr11:65182701..65182825;chr11:65182743..65182833 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_RBP_ID_4185081,Human_RBP_ID_18610479 Human_Splice_Rec_1257538,Human_Splice_Rec_1257546,Human_Splice_Rec_1257588,Human_Splice_Rec_1257596,Human_Splice_Rec_1257604,Human_Splice_Rec_1257646,Human_Splice_Rec_1257688,Human_Splice_Rec_1257700,Human_Splice_Rec_1257742,Human_Splice_Rec_1257744,Human_Splice_Rec_1257750,Human_Splice_Rec_1257760,Human_Splice_Rec_1257766,Human_Splice_Rec_1257778,Human_Splice_Rec_1257784 RMVar_hsa_circ_150587,RMVar_hsa_circ_102811,RMVar_hsa_circ_125191,RMVar_hsa_circ_150588,RMVar_hsa_circ_83684,RMVar_hsa_circ_150589,RMVar_hsa_circ_79907,RMVar_hsa_circ_349640,RMVar_hsa_circ_150590 116791 RMVar_ID_116791 Human_SNP_ID_812167038 m1A Human chr11 - 9716197 9716197 9716197 ATTTCATCTATTCACCTATCACTCTCTTCCTCAAAAATCATCAGTGGCTCATCTTTCCACACTGC ATTTCATCTATTCACCTATCACTCTCTTCCTCGAAAATCATCAGTGGCTCATCTTTCCACACTGC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:9716194..9716314 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus 116792 RMVar_ID_116792 Human_SNP_ID_812173142 m1A Human chr11 - 6611750 6611750 6611750 GGGCCATATCTAACGGGGTTTACGTACTGCCGAGCGCGGCCAACGGAGACGTGAAGCCCGTGGTG GGGCCATATCTAACGGGGTTTACGTACTGCCGGGCGCGGCCAACGGAGACGTGAAGCCCGTGGTG T C AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding exon,CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:6611701..6612200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 2 head and neck Human_RBP_ID_401567,Human_RBP_ID_748694,Human_RBP_ID_988106,Human_RBP_ID_5087192,Human_RBP_ID_5093587,Human_RBP_ID_5644342,Human_RBP_ID_8356588,Human_RBP_ID_22753332 Human_Splice_Rec_1205186,Human_Splice_Rec_1205187,Human_Splice_Rec_1205202,Human_Splice_Rec_1205203,Human_Splice_Rec_1205208,Human_Splice_Rec_1205222 RMVar_hsa_circ_99612,RMVar_hsa_circ_147882 116793 RMVar_ID_116793 Human_SNP_ID_812192901 m1A Human chr11 + 824925 824925 824925 AGACGCCTCCATTACCACTGCGCAGTGAGATGAGGGGACTCACAGTTGCCAAGAGGGGTCTTTGC AGACGCCTCCATTACCACTGCGCAGTGAGATGCGGGGACTCACAGTTGCCAAGAGGGGTCTTTGC A C PNPLA2 Ensembl:ENSG00000177666 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:824876..825100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 1 biliary tract,gallbladder Human_RBP_ID_404755,Human_RBP_ID_988551,Human_RBP_ID_1163655,Human_RBP_ID_17649379,Human_RBP_ID_17802121 116794 RMVar_ID_116794 Human_SNP_ID_812193530 m1A Human chr11 + 106077746 106077746 106077746 GTTTTCCCTGCCAAACGGTTCTGCTTGGTGCCATCCATGGAGGGCGTGCGCTGGGCCTTTTCCTG GTTTTCCCTGCCAAACGGTTCTGCTTGGTGCCGTCCATGGAGGGCGTGCGCTGGGCCTTTTCCTG A G AASDHPPT Ensembl:ENSG00000149313 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:106077695..106077818 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 4 lung Human_RBP_ID_387831,Human_RBP_ID_751330,Human_RBP_ID_985555,Human_RBP_ID_4146076,Human_RBP_ID_5415552,Human_RBP_ID_5435976,Human_RBP_ID_5459897,Human_RBP_ID_8766289,Human_RBP_ID_8940645,Human_RBP_ID_9274373,Human_RBP_ID_17788810,Human_RBP_ID_18417129,Human_RBP_ID_22034908,Human_RBP_ID_23483959 116795 RMVar_ID_116795 Human_SNP_ID_812197302 m1A Human chr11 + 62527519 62527519 62527519 GGGGGTCTTGAAGTGCATCTCAGGCATCTTAAACTTGGGGCCCTTCAGCTTCCCTTCTGGACCTT GGGGGTCTTGAAGTGCATCTCAGGCATCTTAAGCTTGGGGCCCTTCAGCTTCCCTTCTGGACCTT A G NONHSAG008515.2,NONHSAG008515.2:2,NONHSAG008515.2:3,NONHSAG008515.2:4,NONHSAG008515.2:5 RNACentral:URS00009BDEDD,RNACentral:URS00008C0DAB,RNACentral:URS00008C0C25,RNACentral:URS00009C0D48,RNACentral:URS00008C1162 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62527501..62527575 32194978 MeRIP-seq:(Medium) rs138917652 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,head_neck squamous_cell_carcinoma 4 head and neck 116796 RMVar_ID_116796 Human_SNP_ID_812201652 m1A Human chr11 + 94864807 94864807 94864807 GGAGAGAGCTCGCTGGAGGCCCACATCTGGCAAGAGGAGGAGGAGGTGGTGCAGGCCAACAGAAG GGAGAGAGCTCGCTGGAGGCCCACATCTGGCAGGAGGAGGAGGAGGTGGTGCAGGCCAACAGAAG A G AMOTL1 Ensembl:ENSG00000166025 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:94864682..94864808 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_31188,Human_RBP_ID_26319144,Human_RBP_ID_27803942 Human_Splice_Rec_1289216,Human_Splice_Rec_1289217,Human_Splice_Rec_1289238,Human_Splice_Rec_1289239,Human_Splice_Rec_1289249 Human_miRNA_ID_2016175 RMVar_hsa_circ_36405,RMVar_hsa_circ_14570,RMVar_hsa_circ_152562,RMVar_hsa_circ_372603 116797 RMVar_ID_116797 Human_SNP_ID_812216233 m1A Human chr11 + 61967562 61967562 61967562 GGGCTGGCTATGGGCGGCCGGCCGGGGTGGGGAACGAGCGCCGGGTTCCGTCCAAGCACTGTTGA GGGCTGGCTATGGGCGGCCGGCCGGGGTGGGGGACGAGCGCCGGGTTCCGTCCAAGCACTGTTGA A G - - Other Unknown GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HEPG2 cell line,total RNA Untreated chr11:61967251..61967625;chr11:61967120..61967650;chr11:61967301..61967650;chr11:61967323..61967625 26863196 MeRIP-seq:(Medium) rs750898501 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain 116798 RMVar_ID_116798 Human_SNP_ID_812233478 m1A Human chr11 - 57327791 57327791 57327791 GCTCAATGCCAGCCGAGAGAAGATCAAGTCAGACCATCCTGGCATCAGCATCACGGATCTTTCCA GCTCAATGCCAGCCGAGAGAAGATCAAGTCAGTCCATCCTGGCATCAGCATCACGGATCTTTCCA T A SSRP1 Ensembl:ENSG00000149136 Protein coding exon GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:57327751..57327825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_30716,Human_RBP_ID_397564,Human_RBP_ID_749747,Human_RBP_ID_870813,Human_RBP_ID_987302,Human_RBP_ID_1779912,Human_RBP_ID_5343571,Human_RBP_ID_6078810,Human_RBP_ID_8769833,Human_RBP_ID_17465014,Human_RBP_ID_18608777,Human_RBP_ID_22790570,Human_RBP_ID_26318321,Human_RBP_ID_27803430 Human_Splice_Rec_1239506,Human_Splice_Rec_1239507,Human_Splice_Rec_1239536,Human_Splice_Rec_1239537,Human_Splice_Rec_1239552,Human_Splice_Rec_1239553 Human_miRNA_ID_1957089 RMVar_hsa_circ_104852,RMVar_hsa_circ_113105,RMVar_hsa_circ_116074,RMVar_hsa_circ_116869,RMVar_hsa_circ_121817,RMVar_hsa_circ_116659,RMVar_hsa_circ_110723,RMVar_hsa_circ_93401,RMVar_hsa_circ_101879,RMVar_hsa_circ_92673,RMVar_hsa_circ_94097,RMVar_hsa_circ_149735,RMVar_hsa_circ_149739,RMVar_hsa_circ_149743,RMVar_hsa_circ_79897,RMVar_hsa_circ_81368,RMVar_hsa_circ_149741,RMVar_hsa_circ_149742,RMVar_hsa_circ_149740,RMVar_hsa_circ_149737,RMVar_hsa_circ_149738,RMVar_hsa_circ_149736,RMVar_hsa_circ_149733,RMVar_hsa_circ_149734,RMVar_hsa_circ_149732,RMVar_hsa_circ_78264,RMVar_hsa_circ_101451,RMVar_hsa_circ_111815,RMVar_hsa_circ_149746,RMVar_hsa_circ_79048,RMVar_hsa_circ_149748,RMVar_hsa_circ_149750,RMVar_hsa_circ_77591,RMVar_hsa_circ_149751,RMVar_hsa_circ_149749,RMVar_hsa_circ_149747 116799 RMVar_ID_116799 Human_SNP_ID_812240281 m1A Human chr11 + 117282051 117282051 117282051 AATCCTGAACCCTGCCCTTTCCCAGCCCAGCCAGCCTTCCTCACCCCTTCCTGGCTCCCATGGCA AATCCTGAACCCTGCCCTTTCCCAGCCCAGCCCGCCTTCCTCACCCCTTCCTGGCTCCCATGGCA A C RNF214 Ensembl:ENSG00000167257 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:117281980..117282159 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 READ 1 - Human_RBP_ID_226902,Human_RBP_ID_17073861,Human_RBP_ID_18188622,Human_RBP_ID_18934012,Human_RBP_ID_26320647 RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_51895 116800 RMVar_ID_116800 Human_SNP_ID_812254108 m1A Human chr11 + 47579311 47579311 47579311 ACCCTCCGTTCTGTTGCTGCCGGTGAGGCGGGAGAGCGCCGGGGCCGACACGCGCCGTGAGTATG ACCCTCCGTTCTGTTGCTGCCGGTGAGGCGGGGGAGCGCCGGGGCCGACACGCGCCGTGAGTATG A G NDUFS3 Ensembl:ENSG00000213619 Protein coding intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:47579076..47579350 26863410 MeRIP-seq:(Medium) rs1469806098 Functional Loss SNV ICGC 33..33 33 BLCA 1 - Human_RBP_ID_750834,Human_RBP_ID_807999,Human_RBP_ID_4184821,Human_RBP_ID_5110405,Human_RBP_ID_9321384,Human_RBP_ID_19049357,Human_RBP_ID_22432888,Human_RBP_ID_26775763,Human_RBP_ID_27836312 Human_Splice_Rec_1237854,Human_Splice_Rec_1237856,Human_Splice_Rec_1237857,Human_Splice_Rec_1237868,Human_Splice_Rec_1237869,Human_Splice_Rec_1237872,Human_Splice_Rec_1237873,Human_Splice_Rec_1237878,Human_Splice_Rec_1237879,Human_Splice_Rec_1237889,Human_Splice_Rec_1237891,Human_Splice_Rec_1237899 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_149588,RMVar_hsa_circ_88849 116801 RMVar_ID_116801 Human_SNP_ID_812265105 m1A Human chr11 - 64316830 64316830 64316830 GATTGTGCCAGGCGCCAGTTTTTCTTGTTATGACTGTGTATTTTTGTTGATCTATACCCTGTTTC GATTGTGCCAGGCGCCAGTTTTTCTTGTTATGGCTGTGTATTTTTGTTGATCTATACCCTGTTTC T C TRMT112 Ensembl:ENSG00000173113 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64316826..64316850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_31489,Human_RBP_ID_399936,Human_RBP_ID_748795,Human_RBP_ID_1162630,Human_RBP_ID_1458631,Human_RBP_ID_1780946,Human_RBP_ID_2274662,Human_RBP_ID_3377561,Human_RBP_ID_6084304,Human_RBP_ID_8354909,Human_RBP_ID_8946254,Human_RBP_ID_11667294,Human_RBP_ID_18251429,Human_RBP_ID_23206987,Human_RBP_ID_23512400,Human_RBP_ID_24403506,Human_RBP_ID_24460738 Human_miRNA_ID_159566 RMVar_hsa_circ_98464,RMVar_hsa_circ_113069,RMVar_hsa_circ_90322,RMVar_hsa_circ_93854,RMVar_hsa_circ_150468,RMVar_hsa_circ_150470,RMVar_hsa_circ_150471,RMVar_hsa_circ_150469 116802 RMVar_ID_116802 Human_SNP_ID_812282214 m1A Human chr11 - 46382598 46382598 46382598 CCCATCACACGCACCCCAGTTCTCAAACTTGTACTTGCAGTCGGCTGGCGAGAGAGCGGCCCAGG CCCATCACACGCACCCCAGTTCTCAAACTTGTGCTTGCAGTCGGCTGGCGAGAGAGCGGCCCAGG T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:46382051..46382814 32194978 MeRIP-seq:(Medium) rs745326945 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 7 large intestine 116803 RMVar_ID_116803 Human_SNP_ID_812296358 m1A Human chr11 - 108917992 108917992 108917992 ACATACCTTATTTTATTTTCCATATCTTCACTATCTGAATCTTCAGAGCTTCTGTATTTATCTGG ACATACCTTATTTTATTTTCCATATCTTCACTGTCTGAATCTTCAGAGCTTCTGTATTTATCTGG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:108917941..108918042 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain 116804 RMVar_ID_116804 Human_SNP_ID_812323751 m1A Human chr11 + 62138909 62138889 62138910 TCTTTCCACAGGTCCCTGAGAACAATGGAAATAACTCGTGGCCCCACAATGACACGGAGATTGCC TCTTTCCACAGGT_____________________CTCGTGGCCCCACAATGACACGGAGATTGCC TCCCTGAGAACAATGGAAATAA T INCENP Ensembl:ENSG00000149503 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:62138743..62141550 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 14..34 33 LUSC 1 - Human_RBP_ID_32364,Human_RBP_ID_1780478,Human_RBP_ID_2272904,Human_RBP_ID_8770259,Human_RBP_ID_11655149,Human_RBP_ID_17797969 Human_Splice_Rec_1247384,Human_Splice_Rec_1247385,Human_Splice_Rec_1247426,Human_Splice_Rec_1247427,Human_Splice_Rec_1247456,Human_Splice_Rec_1247457 RMVar_hsa_circ_150136,RMVar_hsa_circ_326870 116805 RMVar_ID_116805 Human_SNP_ID_812327344 m1A Human chr11 - 119190341 119190341 119190341 GGCACAAGGAGCAGCAACGCCAGTTTGGACTCACCCCCCCTGGATCTTTGAGGCCACCAGCCCCT GGCACAAGGAGCAGCAACGCCAGTTTGGACTCCCCCCCCCTGGATCTTTGAGGCCACCAGCCCCT T G CCDC153 Ensembl:ENSG00000248712 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119190290..119190444 26863196 MeRIP-seq:(Medium) rs749151879 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 116806 RMVar_ID_116806 Human_SNP_ID_812330769 m1A Human chr11 + 66332181 66332181 66332181 AACAAGTATCAGACAAAGGTGGTGGCAGACACAGGACAGGGCCCTGGGTGGGGCTTGCTGGCGCT AACAAGTATCAGACAAAGGTGGTGGCAGACACCGGACAGGGCCCTGGGTGGGGCTTGCTGGCGCT A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:66332130..66332280 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 116807 RMVar_ID_116807 Human_SNP_ID_812331267 m1A Human chr11 - 64317510 64317510 64317510 GAGTTTGTGCGGCGACATGAAACTGCTTACCCACAATCTGCTGAGCTCGCATGTGCGGGGGGTGG GAGTTTGTGCGGCGACATGAAACTGCTTACCCGCAATCTGCTGAGCTCGCATGTGCGGGGGGTGG T C TRMT112 Ensembl:ENSG00000173113 Protein coding CDS GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEK293T,Wild Type chr11:64317381..64317550;chr11:64317426..64317575;chr11:64317326..64317550 26863196,26863410 MeRIP-seq:(Medium) rs780435157 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate Human_RBP_ID_1265169,Human_RBP_ID_4185043,Human_RBP_ID_5110841,Human_RBP_ID_5138632,Human_RBP_ID_5313670,Human_RBP_ID_5436695,Human_RBP_ID_8354916,Human_RBP_ID_11667317,Human_RBP_ID_17682345,Human_RBP_ID_22433080,Human_RBP_ID_23512417,Human_RBP_ID_26893672 Human_Splice_Rec_1253593,Human_Splice_Rec_1253603,Human_Splice_Rec_1253609 RMVar_hsa_circ_113069,RMVar_hsa_circ_150468 116808 RMVar_ID_116808 Human_SNP_ID_812342628 m1A Human chr11 - 2903279 2903277 2903279 TCCAAGCAGGAGGCTGGCGGAGCAGGGGGCAAAAGTCCAGTTGATCCGGGCAGGGGTGCTGAGTC TCCAAGCAGGAGGCTGGCGGAGCAGGGGGCAA__GTCCAGTTGATCCGGGCAGGGGTGCTGAGTC CTT C SLC22A18AS Ensembl:ENSG00000254827 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2903201..2903444 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 LICA 1 - 116809 RMVar_ID_116809 Human_SNP_ID_812348749 m1A Human chr11 - 78079607 78079607 78079607 TTGGGCTACTGCTCCGGCCTGATTGATAACCTAATCCGGCGGAGGCCGATCGCGACGGCTGGTGA TTGGGCTACTGCTCCGGCCTGATTGATAACCTGATCCGGCGGAGGCCGATCGCGACGGCTGGTGA T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding CDS,CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs534418 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 51 head and neck,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_751380,Human_RBP_ID_4184357,Human_RBP_ID_9276051,Human_RBP_ID_17682689,Human_RBP_ID_17804735,Human_RBP_ID_18974833,Human_RBP_ID_22433211,Human_RBP_ID_22753772,Human_RBP_ID_26410746,Human_RBP_ID_26804018 Human_Splice_Rec_1281771,Human_Splice_Rec_1281773,Human_Splice_Rec_1281777,Human_Splice_Rec_1281781,Human_Splice_Rec_1281791,Human_Splice_Rec_1281795,Human_Splice_Rec_1281799,Human_Splice_Rec_1281801,Human_Splice_Rec_1281805 GWAS_ID_9439,GWAS_ID_9440,GWAS_ID_9441,GWAS_ID_9442,GWAS_ID_9443,GWAS_ID_9444,GWAS_ID_9445,GWAS_ID_9446,GWAS_ID_9447,GWAS_ID_9448,GWAS_ID_9449,GWAS_ID_9450,GWAS_ID_9451,GWAS_ID_9452,GWAS_ID_9453,GWAS_ID_9454,GWAS_ID_9455,GWAS_ID_9456,GWAS_ID_9457,GWAS_ID_9458,GWAS_ID_9459,GWAS_ID_9460,GWAS_ID_9461,GWAS_ID_9462,GWAS_ID_9463,GWAS_ID_9464,GWAS_ID_9465,GWAS_ID_9466,GWAS_ID_9467,GWAS_ID_9468,GWAS_ID_9469,GWAS_ID_9470,GWAS_ID_9471,GWAS_ID_9472,GWAS_ID_9473,GWAS_ID_9474,GWAS_ID_9475,GWAS_ID_9476,GWAS_ID_9477,GWAS_ID_9478,GWAS_ID_9479,GWAS_ID_9480,GWAS_ID_9481,GWAS_ID_9482,GWAS_ID_9483,GWAS_ID_9484,GWAS_ID_9485,GWAS_ID_9486,GWAS_ID_9487,GWAS_ID_9488,GWAS_ID_9489,GWAS_ID_9490,GWAS_ID_9491,GWAS_ID_9492,GWAS_ID_9493,GWAS_ID_9494,GWAS_ID_9495 116810 RMVar_ID_116810 Human_SNP_ID_812350923 m1A Human chr11 - 57426638 57426638 57426638 TTGCTGTCATTATTTTAGGGGACGGTATTCAGAATTCGAGCGCAGGAGCTCCGCTTCTCCACCTG TTGCTGTCATTATTTTAGGGGACGGTATTCAGCATTCGAGCGCAGGAGCTCCGCTTCTCCACCTG T G SLC43A3 Ensembl:ENSG00000134802 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:57426576..57426675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2271851,Human_RBP_ID_4184847,Human_RBP_ID_11642632,Human_RBP_ID_19054776 Human_Splice_Rec_1239708,Human_Splice_Rec_1239709,Human_Splice_Rec_1239734,Human_Splice_Rec_1239735,Human_Splice_Rec_1239760,Human_Splice_Rec_1239761,Human_Splice_Rec_1239785,Human_Splice_Rec_1239818,Human_Splice_Rec_1239819,Human_Splice_Rec_1239844,Human_Splice_Rec_1239845,Human_Splice_Rec_1239886,Human_Splice_Rec_1239887,Human_Splice_Rec_1239897,Human_Splice_Rec_1239908,Human_Splice_Rec_1239909,Human_Splice_Rec_1239922,Human_Splice_Rec_1239923,Human_Splice_Rec_1239952,Human_Splice_Rec_1239953,Human_Splice_Rec_1239958,Human_Splice_Rec_1239959,Human_Splice_Rec_1239963,Human_Splice_Rec_1239968,Human_Splice_Rec_1239969,Human_Splice_Rec_1239975,Human_Splice_Rec_1239978,Human_Splice_Rec_1239979,Human_Splice_Rec_1239983 RMVar_hsa_circ_63092,RMVar_hsa_circ_38126,RMVar_hsa_circ_366261,RMVar_hsa_circ_30822 116811 RMVar_ID_116811 Human_SNP_ID_812357612 m1A Human chr11 + 64307224 64307224 64307224 GTGGTGGGCATTGAGCCTCTCTACATCAAGGCAGAGCCGGCCAGCCCTGACAGTCCAAAGGGTTC GTGGTGGGCATTGAGCCTCTCTACATCAAGGCTGAGCCGGCCAGCCCTGACAGTCCAAAGGGTTC A T ESRRA Ensembl:ENSG00000173153 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:64307126..64307275;chr11:64307140..64307325;chr11:64307129..64307316 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_18159260,Human_RBP_ID_18188265,Human_RBP_ID_26409624 Human_Splice_Rec_1253536,Human_Splice_Rec_1253548,Human_Splice_Rec_1253568,Human_Splice_Rec_1253580 116812 RMVar_ID_116812 Human_SNP_ID_812363758 m1A Human chr11 + 72726878 72726878 72726878 GCACAGGTGGTGAGCGGAAGATGTGGCGCTTCATGGGCACAGGCCGTGGGGTGGGGCGGGGTGCA GCACAGGTGGTGAGCGGAAGATGTGGCGCTTCGTGGGCACAGGCCGTGGGGTGGGGCGGGGTGCA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:72726828..72727022 26863196 MeRIP-seq:(Medium) rs1353413456 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 116813 RMVar_ID_116813 Human_SNP_ID_812390734 m1A Human chr11 - 6683300 6683300 6683300 GTTCCGGCCTCCAAGGGGCGGGCAGAAGTTGGAAACATGCGGCTGTCGGTCGCTGCAGCGATCTC GTTCCGGCCTCCAAGGGGCGGGCAGAAGTTGGGAACATGCGGCTGTCGGTCGCTGCAGCGATCTC T C MRPL17 Ensembl:ENSG00000158042 Protein coding 5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1286018082 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_401894,Human_RBP_ID_751408,Human_RBP_ID_4175064,Human_RBP_ID_5490181,Human_RBP_ID_18416508 116814 RMVar_ID_116814 Human_SNP_ID_812399445 m1A Human chr11 - 65044675 65044675 65044675 TGTCCGTGCCCTCATCTTCCTCCTCTGCCATGACCACCTCCTCCAGGGTACGTCCTCGAAGTTTG TGTCCGTGCCCTCATCTTCCTCCTCTGCCATGGCCACCTCCTCCAGGGTACGTCCTCGAAGTTTG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:65044511..65044825;chr11:65044526..65044758 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 116815 RMVar_ID_116815 Human_SNP_ID_812401530 m1A Human chr11 - 64186630 64186630 64186630 CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCACCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC CGGGTGCGGACCCCGGCCCCCGGCCCACCTCCCCCCCGCCCCCTGCGGCCCGCACCCTCCCCAAC T G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:64186611..64186769 26863196 MeRIP-seq:(Medium) rs1241119971 Functional Loss SNV ICGC 33..33 33 MALY 1 - 116816 RMVar_ID_116816 Human_SNP_ID_812408704 m1A Human chr11 - 61314204 61314204 61314204 CCTCTGCCATATTCTTCTTTGTTCAGCCACACAGAGATGGAACATGAAGTGGCTTGCTTGGACAT CCTCTGCCATATTCTTCTTTGTTCAGCCACACGGAGATGGAACATGAAGTGGCTTGCTTGGACAT T C DDB1 Ensembl:ENSG00000167986 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:61314103..61314230 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 2 bladder,urinary tract Human_RBP_ID_866499,Human_RBP_ID_1457901,Human_RBP_ID_9275636,Human_RBP_ID_22641230 Human_Splice_Rec_1244958,Human_Splice_Rec_1245018,Human_Splice_Rec_1245066,Human_Splice_Rec_1245084,Human_Splice_Rec_1245090,Human_Splice_Rec_1245102,Human_Splice_Rec_1245116,Human_Splice_Rec_1245130 Human_miRNA_ID_2076075 RMVar_hsa_circ_56241,RMVar_hsa_circ_90525,RMVar_hsa_circ_109208,RMVar_hsa_circ_94302,RMVar_hsa_circ_149933,RMVar_hsa_circ_81659,RMVar_hsa_circ_149935,RMVar_hsa_circ_149936,RMVar_hsa_circ_149934,RMVar_hsa_circ_100296,RMVar_hsa_circ_115494,RMVar_hsa_circ_126319,RMVar_hsa_circ_149942,RMVar_hsa_circ_149944,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_374994,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,RMVar_hsa_circ_149949,RMVar_hsa_circ_303375,RMVar_hsa_circ_105900,RMVar_hsa_circ_14110,RMVar_hsa_circ_149955,RMVar_hsa_circ_149956,RMVar_hsa_circ_116195,RMVar_hsa_circ_118249,RMVar_hsa_circ_107992,RMVar_hsa_circ_149961,RMVar_hsa_circ_149962,RMVar_hsa_circ_149960,RMVar_hsa_circ_270307,RMVar_hsa_circ_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_96248,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_149968,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149969,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_308683,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_45648,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_18666,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975 116817 RMVar_ID_116817 Human_SNP_ID_812418932 m1A Human chr11 - 62888691 62888691 62888691 GAAGGGTAGTGGGTCCATGTCAGGCTGAAGTCAGGCCGCGTAGGGGAAGCGGAGCAGCAGCCCTT GAAGGGTAGTGGGTCCATGTCAGGCTGAAGTCGGGCCGCGTAGGGGAAGCGGAGCAGCAGCCCTT T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr11:62888331..62888806;chr11:62888526..62888750;chr11:62888516..62888798 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 12 large intestine 116818 RMVar_ID_116818 Human_SNP_ID_812423052 m1A Human chr11 - 17075168 17075168 17075168 TAGGATAAGGATGCTAAATTCCGTCTGATTCTAATAGAGAGCCGGATTCACCGTTTGGCTCGATA TAGGATAAGGATGCTAAATTCCGTCTGATTCTGATAGAGAGCCGGATTCACCGTTTGGCTCGATA T C RPS13 Ensembl:ENSG00000110700 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:17075117..17075267 32194978 MeRIP-seq:(Medium) rs1059640 Functional Loss SNV COSMIC 33..33 33 breast ductal_carcinoma 2 breast Human_RBP_ID_29989,Human_RBP_ID_393020,Human_RBP_ID_748742,Human_RBP_ID_986480,Human_RBP_ID_1455511,Human_RBP_ID_1777460,Human_RBP_ID_2261461,Human_RBP_ID_3372027,Human_RBP_ID_4155179,Human_RBP_ID_6060123,Human_RBP_ID_8348006,Human_RBP_ID_9001648,Human_RBP_ID_11576495,Human_RBP_ID_17231583,Human_RBP_ID_17348028,Human_RBP_ID_17464027,Human_RBP_ID_17793104,Human_RBP_ID_18249185,Human_RBP_ID_18605727,Human_RBP_ID_23496823,Human_RBP_ID_24459296,Human_RBP_ID_27199981,Human_RBP_ID_27410452,Human_RBP_ID_27616351 Human_Splice_Rec_1214396,Human_Splice_Rec_1214397,Human_Splice_Rec_1214399,Human_Splice_Rec_1214402,Human_Splice_Rec_1214403,Human_Splice_Rec_1214413,Human_Splice_Rec_1214422,Human_Splice_Rec_1214423,Human_Splice_Rec_1214430,Human_Splice_Rec_1214431 RMVar_hsa_circ_35996,RMVar_hsa_circ_110321,RMVar_hsa_circ_127941,RMVar_hsa_circ_80997,RMVar_hsa_circ_104657,RMVar_hsa_circ_148439,RMVar_hsa_circ_148441,RMVar_hsa_circ_148442,RMVar_hsa_circ_148440,RMVar_hsa_circ_52698 116819 RMVar_ID_116819 Human_SNP_ID_812445209 m1A Human chr11 - 377437 377437 377437 GGGGCGCGGTGCCTCAGCCCCCAGGCCGGTACACCACTGGGCCCTGGGGAAGGTCTGAGGAGTCC GGGGCGCGGTGCCTCAGCCCCCAGGCCGGTACGCCACTGGGCCCTGGGGAAGGTCTGAGGAGTCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:377433..377568 32194978 MeRIP-seq:(Medium) rs61876284 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116820 RMVar_ID_116820 Human_SNP_ID_812447349 m1A Human chr11 - 78139567 78139567 78139567 GTGCCGCAGCAATGGCGGCGCTCACAATTGCCACGGGTACTGGCAATTGGTTTTCGGCTTTGGCG GTGCCGCAGCAATGGCGGCGCTCACAATTGCCGCGGGTACTGGCAATTGGTTTTCGGCTTTGGCG T C ALG8 Ensembl:ENSG00000159063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:78139378..78139625;chr11:78139400..78139582;chr11:78139435..78139600 26863196 MeRIP-seq:(Medium) rs1408290909 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_4184360,Human_RBP_ID_18417000 Human_Splice_Rec_1281833,Human_Splice_Rec_1281855,Human_Splice_Rec_1281879,Human_Splice_Rec_1281913,Human_Splice_Rec_1281925,Human_Splice_Rec_1281965,Human_Splice_Rec_1281975,Human_Splice_Rec_1281987,Human_Splice_Rec_1281999,Human_Splice_Rec_1282011,Human_Splice_Rec_1282029,Human_Splice_Rec_1282035 Human_miRNA_ID_2027329,Human_miRNA_ID_2678718,Human_miRNA_ID_3080762 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_80459,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152055 116821 RMVar_ID_116821 Human_SNP_ID_812447354 m1A Human chr11 - 78139567 78139567 78139567 GTGCCGCAGCAATGGCGGCGCTCACAATTGCCACGGGTACTGGCAATTGGTTTTCGGCTTTGGCG GTGCCGCAGCAATGGCGGCGCTCACAATTGCCCCGGGTACTGGCAATTGGTTTTCGGCTTTGGCG T G ALG8 Ensembl:ENSG00000159063 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:78139378..78139625;chr11:78139400..78139582;chr11:78139435..78139600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_4184360,Human_RBP_ID_18417000 Human_Splice_Rec_1281833,Human_Splice_Rec_1281855,Human_Splice_Rec_1281879,Human_Splice_Rec_1281913,Human_Splice_Rec_1281925,Human_Splice_Rec_1281965,Human_Splice_Rec_1281975,Human_Splice_Rec_1281987,Human_Splice_Rec_1281999,Human_Splice_Rec_1282011,Human_Splice_Rec_1282029,Human_Splice_Rec_1282035 Human_miRNA_ID_2027329,Human_miRNA_ID_2678718,Human_miRNA_ID_3080762 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_80459,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152055 116822 RMVar_ID_116822 Human_SNP_ID_812482905 m1A Human chr11 + 78079700 78079700 78079700 GTCAGCTTGGGCGGGGGCAGGCTCCGGGCCTCATCCGGCAGAAACCGTAAGGGTTCTGGGTTCCG GTCAGCTTGGGCGGGGGCAGGCTCCGGGCCTCGTCCGGCAGAAACCGTAAGGGTTCTGGGTTCCG A G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:78079650..78079875 26863196 MeRIP-seq:(Medium) rs955719985 Functional Loss SNV TCGA 33..33 33 THYM 1 - 116823 RMVar_ID_116823 Human_SNP_ID_812483679 m1A Human chr11 + 117315680 117315680 117315680 CTTCGTCGGTCTCCCGGGGCAGCCGCAGCCCCAGGGGGGCGCCCCCCAGGCCGCTGCGCAGGGGC CTTCGTCGGTCTCCCGGGGCAGCCGCAGCCCCTGGGGGGCGCCCCCCAGGCCGCTGCGCAGGGGC A T CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117315631..117315715 26863196 MeRIP-seq:(Medium) rs1006804785 Functional Loss SNV ICGC 33..33 33 THCA 1 - 116824 RMVar_ID_116824 Human_SNP_ID_812485425 m1A Human chr11 + 117138591 117138591 117138591 GCACGGGAAGGAGGAGCAGATCTGCTGACCTCAGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC GCACGGGAAGGAGGAGCAGATCTGCTGACCTCGGGGCCTGACAGTGTGGGACAGGCTCTTCTTTC A G - - Other Unknown GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs560621 Functional Loss SNV ICGC 33..33 33 LICA 1 - 116825 RMVar_ID_116825 Human_SNP_ID_812488891 m1A Human chr11 - 67486945 67486945 67486945 GGCACAAACCCTCACCCTGACCCCCAAGGAGAAGTCCAGTCCCCGGCCTGCAGACGGCATAAGGG GGCACAAACCCTCACCCTGACCCCCAAGGAGAGGTCCAGTCCCCGGCCTGCAGACGGCATAAGGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:67486943..67487150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116826 RMVar_ID_116826 Human_SNP_ID_812489416 m1A Human chr11 + 610300 610300 610300 TCAGGCAGGTGTTCTCCGAGCTGCCCTTTCCCAGTCACGTGCTTCCGGAACCCGGGTTCCCAGAC TCAGGCAGGTGTTCTCCGAGCTGCCCTTTCCCGGTCACGTGCTTCCGGAACCCGGGTTCCCAGAC A G PHRF1 Ensembl:ENSG00000070047 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:610250..610347 26863196 MeRIP-seq:(Medium) rs201244128 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_18609252,Human_RBP_ID_22790725,Human_RBP_ID_26892026 Human_Splice_Rec_1193783,Human_Splice_Rec_1193817,Human_Splice_Rec_1193851,Human_Splice_Rec_1193885,Human_Splice_Rec_1193919 Human_miRNA_ID_2037255,Human_miRNA_ID_2347958 RMVar_hsa_circ_123643,RMVar_hsa_circ_147421 116827 RMVar_ID_116827 Human_SNP_ID_812497417 m1A Human chr11 - 62717015 62717015 62717015 TCGCCGAAACAACCGAAACAAGCGTAACCGGCAGAACCGAAGCCGGGGCCAAGGCTATGGTGAGT TCGCCGAAACAACCGAAACAAGCGTAACCGGCTGAACCGAAGCCGGGGCCAAGGCTATGGTGAGT T A HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:62715501..62717050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_32012,Human_RBP_ID_9362364,Human_RBP_ID_26803660 Human_Splice_Rec_1249209,Human_Splice_Rec_1249259 RMVar_hsa_circ_113516,RMVar_hsa_circ_104086,RMVar_hsa_circ_150243,RMVar_hsa_circ_150244,RMVar_hsa_circ_103708,RMVar_hsa_circ_81551,RMVar_hsa_circ_51077,RMVar_hsa_circ_150249,RMVar_hsa_circ_150250,RMVar_hsa_circ_63600,RMVar_hsa_circ_53080,RMVar_hsa_circ_354740,RMVar_hsa_circ_365005,RMVar_hsa_circ_346774 116828 RMVar_ID_116828 Human_SNP_ID_812517179 m1A Human chr11 - 47410150 47410150 47410150 CCCTTTCCAAGAGCTCCAGGGCAAGGGCAGTGAGGAAGAGGAGCCTTGGGCCCGCCATGCCACAG CCCTTTCCAAGAGCTCCAGGGCAAGGGCAGTGTGGAAGAGGAGCCTTGGGCCCGCCATGCCACAG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47410059..47410252 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 116829 RMVar_ID_116829 Human_SNP_ID_812517442 m1A Human chr11 + 124878642 124878642 124878642 CAATGCCTGAGAGAAGTCACCTGACGGAGCCCAGCTCCAGTGGAGGGTGCCTGGTCACCCCATCC CAATGCCTGAGAGAAGTCACCTGACGGAGCCCGGCTCCAGTGGAGGGTGCCTGGTCACCCCATCC A G ROBO3 Ensembl:ENSG00000154134 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:124878591..124878891 32194978 MeRIP-seq:(Medium) rs1357166145 Functional Loss SNV COSMIC 33..33 33 breast luminal_NS_carcinoma 3 breast Human_Splice_Rec_1312728,Human_Splice_Rec_1312780,Human_Splice_Rec_1312802,Human_Splice_Rec_1312816,Human_Splice_Rec_1312830,Human_Splice_Rec_1312856,Human_Splice_Rec_1312870,Human_Splice_Rec_1312898,Human_Splice_Rec_1312904,Human_Splice_Rec_1312920,Human_Splice_Rec_1312950,Human_Splice_Rec_1312962 116830 RMVar_ID_116830 Human_SNP_ID_812520246 m1A Human chr11 + 2884935 2884935 2884935 GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC GCGACTGGAGCCGGGGCCGGAGCCGGAGCCGGGGCCGGGGCCGGGGCCGGGGCCAGGACCGCGAC A G NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:2884886..2885036 26863196 MeRIP-seq:(Medium) rs191294997 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 7 liver 116831 RMVar_ID_116831 Human_SNP_ID_812525886 m1A Human chr11 - 65505553 65505553 65505553 CTAGATCAAAAGGCACGGGGTGGCGATGTGGCAGAGAAGTTGCTTGTGGGGAGACCTTGCTTTTA CTAGATCAAAAGGCACGGGGTGGCGATGTGGCGGAGAAGTTGCTTGTGGGGAGACCTTGCTTTTA T C TALAM1-001,TALAM1-001:2,TALAM1-001:3,L13304-001,L13705-009,TALAM1-001:4 RNACentral:URS00008BAD39,RNACentral:URS00008B3D99,RNACentral:URS0000ABD7D9,RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008B30DF lincRNA,lincRNA,lincRNA,scRNA,misc_RNA,lincRNA intron,intron,exon,intron,intron,intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:65505438..65505957 26863196 MeRIP-seq:(Medium) rs1016390841 Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - 116832 RMVar_ID_116832 Human_SNP_ID_812527586 m1A Human chr11 + 68841810 68841810 68841810 GTCAGCTACGGAGGTGCGGCAGCGGCAGCGGCAGCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC GTCAGCTACGGAGGTGCGGCAGCGGCAGCGGCGGCGGCGGCGGCGGCGGCGGCGGTGGAGTGAAC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr11:68841704..68841900;chr11:68841733..68841894;chr11:68841732..68841876 26863196 MeRIP-seq:(Medium) rs1000188907 Functional Loss SNV COSMIC 33..33 33 biliary_tract adenocarcinoma,gallbladder adenocarcinoma 2 biliary tract,gallbladder 116833 RMVar_ID_116833 Human_SNP_ID_812556847 m1A Human chr11 - 77872316 77872316 77872316 CACTTAGTGATTTATTCTCCTCTTAAGGCTCCATCAGCAGGTGGAATGGAAGACACCTCCCACCC CACTTAGTGATTTATTCTCCTCTTAAGGCTCCCTCAGCAGGTGGAATGGAAGACACCTCCCACCC T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:77872295..77876981 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 10 large intestine RMVar_hsa_circ_151968 116834 RMVar_ID_116834 Human_SNP_ID_812586124 m1A Human chr11 - 534353 534353 534353 TCCTTGGCAGGTGGGGCAGGAGACCCTGTAGGAGGACCCCGGGCCGCAGGCCCCTGAGGAGCGAT TCCTTGGCAGGTGGGGCAGGAGACCCTGTAGGTGGACCCCGGGCCGCAGGCCCCTGAGGAGCGAT T A HRAS Ensembl:ENSG00000174775 Protein coding 5'UTR GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:534178..534432 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_259346,Human_RBP_ID_750462,Human_RBP_ID_3938766,Human_RBP_ID_4184543,Human_RBP_ID_5313450,Human_RBP_ID_22537183,Human_RBP_ID_23508462 Human_Splice_Rec_1193538,Human_Splice_Rec_1193546,Human_Splice_Rec_1193558,Human_Splice_Rec_1193568,Human_Splice_Rec_1193578,Human_Splice_Rec_1193596,Human_Splice_Rec_1193600 RMVar_hsa_circ_118031,RMVar_hsa_circ_147412 116835 RMVar_ID_116835 Human_SNP_ID_812614624 m1A Human chr11 + 20054160 20054160 20054160 GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGACACCGCTGCCAATTCCCCCTTTTCCTCTGGCT GTTACGGTCCCATTCTGCAGGAGGCCTTCAGGTCACCGCTGCCAATTCCCCCTTTTCCTCTGGCT A T NAV2 Ensembl:ENSG00000166833 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:20054076..20054230 26863196 MeRIP-seq:(Medium) rs766953407 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1220000,Human_Splice_Rec_1220001,Human_Splice_Rec_1220074,Human_Splice_Rec_1220075,Human_Splice_Rec_1220150,Human_Splice_Rec_1220151,Human_Splice_Rec_1220224,Human_Splice_Rec_1220225,Human_Splice_Rec_1220298,Human_Splice_Rec_1220299,Human_Splice_Rec_1220374,Human_Splice_Rec_1220375,Human_Splice_Rec_1220444,Human_Splice_Rec_1220445,Human_Splice_Rec_1220494,Human_Splice_Rec_1220495 Human_miRNA_ID_2945643,Human_miRNA_ID_2945644 RMVar_hsa_circ_484,RMVar_hsa_circ_107272,RMVar_hsa_circ_148647,RMVar_hsa_circ_36342,RMVar_hsa_circ_82910,RMVar_hsa_circ_148654,RMVar_hsa_circ_94749,RMVar_hsa_circ_148658,RMVar_hsa_circ_11275,RMVar_hsa_circ_100448,RMVar_hsa_circ_148660,RMVar_hsa_circ_83061,RMVar_hsa_circ_148663,RMVar_hsa_circ_527,RMVar_hsa_circ_29438,RMVar_hsa_circ_70211,RMVar_hsa_circ_322464,RMVar_hsa_circ_11838,RMVar_hsa_circ_22991,RMVar_hsa_circ_31331,RMVar_hsa_circ_50864,RMVar_hsa_circ_25909,RMVar_hsa_circ_148672,RMVar_hsa_circ_300836,RMVar_hsa_circ_312011,RMVar_hsa_circ_364513,RMVar_hsa_circ_377604,RMVar_hsa_circ_339899,RMVar_hsa_circ_307639,RMVar_hsa_circ_7249,RMVar_hsa_circ_20683,RMVar_hsa_circ_148674,RMVar_hsa_circ_148675,RMVar_hsa_circ_148673 116836 RMVar_ID_116836 Human_SNP_ID_812619621 m1A Human chr11 - 2953682 2953682 2953682 TCCCATTGTACTGAGTTCCACCAGTGGGGAGAATAGGCCAGCGTGCTCTTTATCAGCTGTTAGGT TCCCATTGTACTGAGTTCCACCAGTGGGGAGAGTAGGCCAGCGTGCTCTTTATCAGCTGTTAGGT T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2001006 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_6065699,Human_RBP_ID_17794275 GWAS_ID_6814,GWAS_ID_6815,GWAS_ID_6816,GWAS_ID_6817 RMVar_hsa_circ_47327,RMVar_hsa_circ_77496,RMVar_hsa_circ_126801,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147580,RMVar_hsa_circ_147581,RMVar_hsa_circ_147582,RMVar_hsa_circ_268286,RMVar_hsa_circ_268535,RMVar_hsa_circ_329952,RMVar_hsa_circ_347828,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_147583,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585 116837 RMVar_ID_116837 Human_SNP_ID_812620951 m1A Human chr11 + 64349422 64349422 64349422 GCGTGAGCTGGAGCAGGCGGCTCTCGAGCGCCAGGAATTTCTGCGAGAAAAGGAAAGCCAGCACC GCGTGAGCTGGAGCAGGCGGCTCTCGAGCGCCTGGAATTTCTGCGAGAAAAGGAAAGCCAGCACC A T CCDC88B Ensembl:ENSG00000168071 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64349371..64349622 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung Human_RBP_ID_865134,Human_RBP_ID_26320070,Human_RBP_ID_27803551 Human_Splice_Rec_1253668,Human_Splice_Rec_1253669,Human_Splice_Rec_1253720,Human_Splice_Rec_1253721,Human_Splice_Rec_1253756,Human_Splice_Rec_1253757,Human_Splice_Rec_1253788,Human_Splice_Rec_1253789,Human_Splice_Rec_1253796,Human_Splice_Rec_1253797,Human_Splice_Rec_1253802,Human_Splice_Rec_1253803 RMVar_hsa_circ_63299 116838 RMVar_ID_116838 Human_SNP_ID_812624971 m1A Human chr11 + 709584 709584 709584 GTGGCAGCCTGGGCCGGTCCGACGGTGTGGCCAAGATGAGCCCCAAGGACCTGTTTGGTGAGTGA GTGGCAGCCTGGGCCGGTCCGACGGTGTGGCCTAGATGAGCCCCAAGGACCTGTTTGGTGAGTGA A T EPS8L2 Ensembl:ENSG00000177106 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:697895..709590 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_RBP_ID_18973077,Human_RBP_ID_19048892 Human_Splice_Rec_1194438,Human_Splice_Rec_1194439,Human_Splice_Rec_1194448,Human_Splice_Rec_1194454,Human_Splice_Rec_1194455,Human_Splice_Rec_1194494,Human_Splice_Rec_1194495,Human_Splice_Rec_1194536,Human_Splice_Rec_1194537,Human_Splice_Rec_1194544,Human_Splice_Rec_1194545,Human_Splice_Rec_1194562,Human_Splice_Rec_1194563,Human_Splice_Rec_1194602,Human_Splice_Rec_1194642,Human_Splice_Rec_1194646,Human_Splice_Rec_1194647,Human_Splice_Rec_1194652,Human_Splice_Rec_1194653,Human_Splice_Rec_1194694,Human_Splice_Rec_1194695,Human_Splice_Rec_1194702,Human_Splice_Rec_1194703,Human_Splice_Rec_1194710,Human_Splice_Rec_1194711,Human_Splice_Rec_1194718,Human_Splice_Rec_1194722,Human_Splice_Rec_1194723,Human_Splice_Rec_1194760,Human_Splice_Rec_1194761,Human_Splice_Rec_1194797 RMVar_hsa_circ_88989,RMVar_hsa_circ_147442 116839 RMVar_ID_116839 Human_SNP_ID_812634865 m1A Human chr11 - 77622672 77622672 77622672 ATTTAAACTTTAAAGTTTTCTGTTTGTTTAGAACAAGGACAGGGGGACATCCCTACATTTTACAC ATTTAAACTTTAAAGTTTTCTGTTTGTTTAGAGCAAGGACAGGGGGACATCCCTACATTTTACAC T C CLNS1A Ensembl:ENSG00000074201 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:77622650..77622727 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 CESC 1 - Human_RBP_ID_870319,Human_RBP_ID_9362789,Human_RBP_ID_11723363,Human_RBP_ID_22895201,Human_RBP_ID_23207057,Human_RBP_ID_24542986,Human_RBP_ID_26319037,Human_RBP_ID_27207430,Human_RBP_ID_27803857 Human_Splice_Rec_1281316,Human_Splice_Rec_1281326,Human_Splice_Rec_1281350,Human_Splice_Rec_1281362,Human_Splice_Rec_1281374,Human_Splice_Rec_1281378,Human_Splice_Rec_1281380 Human_miRNA_ID_2444116 RMVar_hsa_circ_151910,RMVar_hsa_circ_127604,RMVar_hsa_circ_151908,RMVar_hsa_circ_123342,RMVar_hsa_circ_91256,RMVar_hsa_circ_94520,RMVar_hsa_circ_151912,RMVar_hsa_circ_151911,RMVar_hsa_circ_151918,RMVar_hsa_circ_280548,RMVar_hsa_circ_345318,RMVar_hsa_circ_151909,RMVar_hsa_circ_341566,RMVar_hsa_circ_271847,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_306901,RMVar_hsa_circ_151916,RMVar_hsa_circ_151917,RMVar_hsa_circ_376873,RMVar_hsa_circ_151921,RMVar_hsa_circ_289519,RMVar_hsa_circ_151920 116840 RMVar_ID_116840 Human_SNP_ID_812673760 m1A Human chr11 + 118902229 118902229 118902229 CAGGCGTGAGGCTGTCCTGGCCCAGCCTCTGTATCATCATGTTCATCTGCTGCCCCATGTCCCCA CAGGCGTGAGGCTGTCCTGGCCCAGCCTCTGTGTCATCATGTTCATCTGCTGCCCCATGTCCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:118902180..118902281 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116841 RMVar_ID_116841 Human_SNP_ID_812679121 m1A Human chr11 - 32091401 32091401 32091401 CTCGTCCGGGGTGAGCTGGTCGAAGGTCTTGGAGTCCTCCTTGCCCAGGAAGGCCTCGTGGTCGT CTCGTCCGGGGTGAGCTGGTCGAAGGTCTTGGGGTCCTCCTTGCCCAGGAAGGCCTCGTGGTCGT T C - - Other Unknown GSE70485:GSM1782894,GSM1782895;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,total RNA rearranged at 60c;HTR8/Svneo,Hypoxia IP chr11:32091376..32091400 26863196,32194978 MeRIP-seq:(Medium) rs1423439187 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine 116842 RMVar_ID_116842 Human_SNP_ID_812688538 m1A Human chr11 - 22853692 22853692 22853692 CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCATCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT CTTCTTCTTTCTTCTTCTTCCTCTTCCTCTTCTTCCTTTTCCTCTTCCTCTCCTCCTTCCTTCTT T A CCDC179 Ensembl:ENSG00000255359 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:22853674..22853739 26863196 MeRIP-seq:(Medium) rs7395367 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver GWAS_ID_12168,GWAS_ID_12169,GWAS_ID_12170,GWAS_ID_12171,GWAS_ID_12172,GWAS_ID_12173,GWAS_ID_12174,GWAS_ID_12175,GWAS_ID_12176,GWAS_ID_12177,GWAS_ID_12178,GWAS_ID_12179,GWAS_ID_12180,GWAS_ID_12181,GWAS_ID_12182,GWAS_ID_12183,GWAS_ID_12184,GWAS_ID_12185,GWAS_ID_12186,GWAS_ID_12187,GWAS_ID_12188 116843 RMVar_ID_116843 Human_SNP_ID_812693294 m1A Human chr11 - 47720031 47720031 47720031 GCCATCTTTGGTAAAAAAGTGGCAGAGTATCCAGCGTGAGTTAGATGAAGAGGACAATTCTAGTT GCCATCTTTGGTAAAAAAGTGGCAGAGTATCCCGCGTGAGTTAGATGAAGAGGACAATTCTAGTT T G FNBP4 Ensembl:ENSG00000109920 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:47719926..47720131 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_2271121,Human_RBP_ID_11637742,Human_RBP_ID_23507852,Human_RBP_ID_24888784 Human_Splice_Rec_1238278,Human_Splice_Rec_1238284 RMVar_hsa_circ_72508,RMVar_hsa_circ_99805,RMVar_hsa_circ_102697,RMVar_hsa_circ_149620,RMVar_hsa_circ_149621,RMVar_hsa_circ_317026,RMVar_hsa_circ_378749,RMVar_hsa_circ_149622 116844 RMVar_ID_116844 Human_SNP_ID_812714353 m1A Human chr11 - 62591472 62591472 62591472 TCGGTACAGGAGAGTCGCTATGGCGGCGGTGGATTCGGATGTCGAATCGCTGCCGCGTGGGGGGT TCGGTACAGGAGAGTCGCTATGGCGGCGGTGGGTTCGGATGTCGAATCGCTGCCGCGTGGGGGGT T C AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:62591421..62591505 26863196 MeRIP-seq:(Medium) rs778420150 Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_4184944,Human_RBP_ID_11656878,Human_RBP_ID_23124530,Human_RBP_ID_23207317 Human_Splice_Rec_1247707,Human_Splice_Rec_1247743,Human_Splice_Rec_1247759,Human_Splice_Rec_1247781,Human_Splice_Rec_1247791 116845 RMVar_ID_116845 Human_SNP_ID_812724819 m1A Human chr11 + 73787989 73787989 73787989 GCGCAGCAGCAAAGGATGAGCGGAACCTTGGAAAAGGTAACGTAGATTCCACGCACGCGGGGCGC GCGCAGCAGCAAAGGATGAGCGGAACCTTGGATAAGGTAACGTAGATTCCACGCACGCGGGGCGC A T MRPL48 Ensembl:ENSG00000175581 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:73787938..73788033 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung non_small_cell_carcinoma 4 lung Human_RBP_ID_4185269 Human_Splice_Rec_1276583,Human_Splice_Rec_1276599,Human_Splice_Rec_1276613,Human_Splice_Rec_1276629,Human_Splice_Rec_1276637,Human_Splice_Rec_1276649,Human_Splice_Rec_1276659,Human_Splice_Rec_1276677,Human_Splice_Rec_1276687,Human_Splice_Rec_1276701,Human_Splice_Rec_1276711,Human_Splice_Rec_1276715 RMVar_hsa_circ_120733,RMVar_hsa_circ_151637 116846 RMVar_ID_116846 Human_SNP_ID_812750362 m1A Human chr11 + 124675263 124675263 124675263 TCTTTAGGTTCCATAGGCAGTTCTTACCAAGAAGATGTCGATTCCATTCTCCAACACCCACTACC TCTTTAGGTTCCATAGGCAGTTCTTACCAAGAGGATGTCGATTCCATTCTCCAACACCCACTACC A G SPA17 Ensembl:ENSG00000064199 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:124675259..124675377;chr11:124675258..124675359 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_391058 Human_Splice_Rec_1312414,Human_Splice_Rec_1312428 116847 RMVar_ID_116847 Human_SNP_ID_812757121 m1A Human chr11 - 112226484 112226484 112226484 GGTGGCTCGCGCTGAAGGAGATGCGGCGGGACACTTGTGCCTGGCAGCGACGGCCACCACCTTCC GGTGGCTCGCGCTGAAGGAGATGCGGCGGGACGCTTGTGCCTGGCAGCGACGGCCACCACCTTCC T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEK293T cell line,total RNA;HEPG2 cell line,mRNA untreated chr11:112226385..112226518;chr11:112226364..112228675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 116848 RMVar_ID_116848 Human_SNP_ID_812780890 m1A Human chr11 - 65088101 65088101 65088101 TAGCCACAAGCAAGGGGGCTCAGGAGGGGCCCACGCGGATGTGAGGGTTCATGAGTGGGTCCAGG TAGCCACAAGCAAGGGGGCTCAGGAGGGGCCCGCGCGGATGTGAGGGTTCATGAGTGGGTCCAGG T C TMEM262 Ensembl:ENSG00000187066 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65088051..65088125 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 116849 RMVar_ID_116849 Human_SNP_ID_812789446 m1A Human chr11 - 65111994 65111990 65111994 GTGGGGGCCATGGTCTCCGCTCCGCCGGAGAGAGAGGGCGCTCACAATAGTCAGTCAAGGAAACA GTGGGGGCCATGGTCTCCGCTCCGCCGGAGAG____GGCGCTCACAATAGTCAGTCAAGGAAACA CCTCT C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:65111943..65112092 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..36 33 ESCA 1 - 116850 RMVar_ID_116850 Human_SNP_ID_812796207 m1A Human chr11 - 533871 533871 533871 CCTGTTGGACATCCTGGATACCGCCGGCCAGGAGGAGTACAGCGCCATGCGGGACCAGTACATGC CCTGTTGGACATCCTGGATACCGCCGGCCAGGGGGAGTACAGCGCCATGCGGGACCAGTACATGC T C HRAS Ensembl:ENSG00000174775 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:533820..533977 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 25 head and neck Human_RBP_ID_397491,Human_RBP_ID_4186495,Human_RBP_ID_5110998,Human_RBP_ID_18973033 Human_Splice_Rec_1193530,Human_Splice_Rec_1193540,Human_Splice_Rec_1193548,Human_Splice_Rec_1193560,Human_Splice_Rec_1193570,Human_Splice_Rec_1193580,Human_Splice_Rec_1193598 Human_miRNA_ID_2975663 RMVar_hsa_circ_118031,RMVar_hsa_circ_147412 116851 RMVar_ID_116851 Human_SNP_ID_812811964 m1A Human chr11 + 71444107 71444107 71444107 GCATGTCCGGTGACGATGTCCACCACAGGGCCAGTCAGGGCGCAGCTGTACTGGTCACAAGCCAT GCATGTCCGGTGACGATGTCCACCACAGGGCCGGTCAGGGCGCAGCTGTACTGGTCACAAGCCAT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:71444057..71444163 26863196 MeRIP-seq:(Medium) rs1790334 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 7 head and neck Clinvar_Rec_360,Clinvar_Rec_8585 GWAS_ID_9349,GWAS_ID_9350,GWAS_ID_9351,GWAS_ID_9352,GWAS_ID_9353 116852 RMVar_ID_116852 Human_SNP_ID_812833850 m1A Human chr11 + 64193082 64193082 64193082 GAGAAGCTGTGTGTTCCTTTCCCCTCAGGTCAATGAGCTGAAGGAGAAAGGCAACAAGGCCCTGA GAGAAGCTGTGTGTTCCTTTCCCCTCAGGTCAGTGAGCTGAAGGAGAAAGGCAACAAGGCCCTGA A G STIP1 Ensembl:ENSG00000168439 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64193076..64193337 32194978 MeRIP-seq:(Medium) rs147750881 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 5 breast Human_RBP_ID_31407,Human_RBP_ID_808621,Human_RBP_ID_871649,Human_RBP_ID_4185011,Human_RBP_ID_5461039,Human_RBP_ID_8774315,Human_RBP_ID_9362416,Human_RBP_ID_18188536,Human_RBP_ID_18610202,Human_RBP_ID_22435425,Human_RBP_ID_24913784,Human_RBP_ID_26317799,Human_RBP_ID_26804840,Human_RBP_ID_26893525,Human_RBP_ID_27804545 Human_Splice_Rec_1252444,Human_Splice_Rec_1252470,Human_Splice_Rec_1252496,Human_Splice_Rec_1252504,Human_Splice_Rec_1252530,Human_Splice_Rec_1252538,Human_Splice_Rec_1252540 RMVar_hsa_circ_109104,RMVar_hsa_circ_150404,RMVar_hsa_circ_303043,RMVar_hsa_circ_311448,RMVar_hsa_circ_322090,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_316317,RMVar_hsa_circ_303371,RMVar_hsa_circ_55185,RMVar_hsa_circ_128188,RMVar_hsa_circ_150406,RMVar_hsa_circ_150407,RMVar_hsa_circ_150405,RMVar_hsa_circ_150403 116853 RMVar_ID_116853 Human_SNP_ID_812834905 m1A Human chr11 - 46097184 46097184 46097184 TTTGAAAAGCTTACTCTGGCTTGCGAGAGAATATACCTTAGCGGGGCTAGGGTAGAATTGGGGAG TTTGAAAAGCTTACTCTGGCTTGCGAGAGAATTTACCTTAGCGGGGCTAGGGTAGAATTGGGGAG T A PHF21A Ensembl:ENSG00000135365 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:46097150..46097277 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus RMVar_hsa_circ_9666,RMVar_hsa_circ_113581,RMVar_hsa_circ_149313,RMVar_hsa_circ_149315,RMVar_hsa_circ_109827,RMVar_hsa_circ_25414,RMVar_hsa_circ_313791,RMVar_hsa_circ_149319,RMVar_hsa_circ_42034 116854 RMVar_ID_116854 Human_SNP_ID_812843040 m1A Human chr11 - 66624307 66624307 66624307 GCCCCTTCTTCTGACCCTTGGTGGAGAGTTCCACGTTGATGCGCTTGCCCTTCACTTCTTTGCCG GCCCCTTCTTCTGACCCTTGGTGGAGAGTTCCCCGTTGATGCGCTTGCCCTTCACTTCTTTGCCG T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66624256..66624335 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 9 kidney 116855 RMVar_ID_116855 Human_SNP_ID_812849147 m1A Human chr11 - 68032189 68032189 68032189 CTTTGGTCCTACCTGCACGTGCAGCCTGGGCCAGGGCCCGCAGCAGCATAGGCGTGGTCAGGCAG CTTTGGTCCTACCTGCACGTGCAGCCTGGGCCTGGGCCCGCAGCAGCATAGGCGTGGTCAGGCAG T A - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:68032151..68032250 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma,KIRC 4 kidney 116856 RMVar_ID_116856 Human_SNP_ID_812868426 m1A Human chr11 - 14281700 14281700 14281700 TTGGAATTTCAGGTAACACAGGAAGAAGGACAACAGTTAGCACGGCAGCTTAAGGTAACATACAT TTGGAATTTCAGGTAACACAGGAAGAAGGACAGCAGTTAGCACGGCAGCTTAAGGTAACATACAT T C RRAS2 Ensembl:ENSG00000133818 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:14281652..14281751 26863196 MeRIP-seq:(Medium) rs782747533 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver Human_RBP_ID_6058143,Human_RBP_ID_11570170 Human_Splice_Rec_1212858,Human_Splice_Rec_1212859,Human_Splice_Rec_1212868,Human_Splice_Rec_1212869,Human_Splice_Rec_1212876,Human_Splice_Rec_1212877,Human_Splice_Rec_1212886,Human_Splice_Rec_1212887,Human_Splice_Rec_1212896,Human_Splice_Rec_1212897,Human_Splice_Rec_1212906,Human_Splice_Rec_1212907,Human_Splice_Rec_1212916,Human_Splice_Rec_1212917,Human_Splice_Rec_1212926,Human_Splice_Rec_1212927,Human_Splice_Rec_1212938,Human_Splice_Rec_1212946 RMVar_hsa_circ_25591 116857 RMVar_ID_116857 Human_SNP_ID_812875515 m1A Human chr11 + 67612180 67612176 67612180 ACGTTTCGTGAGGGGGGATGCCCGGCCGGCCGAGATCGACTCCCTGTGGGAGATCAGCAAGCAGA ACGTTTCGTGAGGGGGGATGCCCGGCCGG____GATCGACTCCCTGTGGGAGATCAGCAAGCAGA GCCGA G NDUFV1 Ensembl:ENSG00000167792 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h chr11:67612098..67612211;chr11:67612104..67612202 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 30..33 33 COAD 1 - Human_RBP_ID_226914,Human_RBP_ID_402153,Human_RBP_ID_871782,Human_RBP_ID_3940962,Human_RBP_ID_5110551,Human_RBP_ID_5138700,Human_RBP_ID_5314339,Human_RBP_ID_17648815,Human_RBP_ID_17804688,Human_RBP_ID_18159295,Human_RBP_ID_18972402,Human_RBP_ID_22434678,Human_RBP_ID_22491698,Human_RBP_ID_23517213,Human_RBP_ID_26318890 Human_Splice_Rec_1267120,Human_Splice_Rec_1267121,Human_Splice_Rec_1267136,Human_Splice_Rec_1267137,Human_Splice_Rec_1267168,Human_Splice_Rec_1267169,Human_Splice_Rec_1267186,Human_Splice_Rec_1267187,Human_Splice_Rec_1267224,Human_Splice_Rec_1267225,Human_Splice_Rec_1267302,Human_Splice_Rec_1267303,Human_Splice_Rec_1267322,Human_Splice_Rec_1267323,Human_Splice_Rec_1267328,Human_Splice_Rec_1267329,Human_Splice_Rec_1267334,Human_Splice_Rec_1267336,Human_Splice_Rec_1267337,Human_Splice_Rec_1267339 Human_miRNA_ID_340089,Human_miRNA_ID_1692490,Human_miRNA_ID_2868109 RMVar_hsa_circ_151093,RMVar_hsa_circ_114392 116858 RMVar_ID_116858 Human_SNP_ID_812899769 m1A Human chr11 - 62807542 62807539 62807543 GATCCTCAAGTACTTCCAGTCTGTCACCTCCAACCGGTGGCTCATGGTCAAAATCTTCCTCATCC GATCCTCAAGTACTTCCAGTCTGTCACCTCC____GGTGGCTCATGGTCAAAATCTTCCTCATCC CGGTT C STX5 Ensembl:ENSG00000162236 Protein coding CDS GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss DEL TCGA 32..35 33 HNSC 1 - Human_RBP_ID_18609861 Human_Splice_Rec_1249776,Human_Splice_Rec_1249816,Human_Splice_Rec_1249834,Human_Splice_Rec_1249854 RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 116859 RMVar_ID_116859 Human_SNP_ID_812900106 m1A Human chr11 - 64854316 64854316 64854316 GCGCAGACATGAGTGATGGCGCCCGGCCCCGCACCTGCCATTTGCACGCCCGGCCGGGAGGCAGA GCGCAGACATGAGTGATGGCGCCCGGCCCCGCCCCTGCCATTTGCACGCCCGGCCGGGAGGCAGA T G EHD1 Ensembl:ENSG00000110047 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64854272..64854373 32194978 MeRIP-seq:(Medium) rs758470055 Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 3 stomach Human_RBP_ID_9322157,Human_RBP_ID_22433084 Human_miRNA_ID_2180953,Human_miRNA_ID_2183055,Human_miRNA_ID_3065916 RMVar_hsa_circ_150517,RMVar_hsa_circ_89553,RMVar_hsa_circ_97999,RMVar_hsa_circ_150518 116860 RMVar_ID_116860 Human_SNP_ID_812903187 m1A Human chr11 + 65499114 65499114 65499114 GGGGCAGGCGGAGCTTGAGGAAACCGCAGATAAGTTTTTTTCTCTTTGAAAGATAGAGATTAATA GGGGCAGGCGGAGCTTGAGGAAACCGCAGATACGTTTTTTTCTCTTTGAAAGATAGAGATTAATA A C MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65499051..65499150 32194978 MeRIP-seq:(Medium) rs766966793 Functional Loss SNV TCGA 33..33 33 CHOL 1 - Human_RBP_ID_228201,Human_RBP_ID_274843,Human_RBP_ID_752229,Human_RBP_ID_807129,Human_RBP_ID_1126450,Human_RBP_ID_1162901,Human_RBP_ID_1459102,Human_RBP_ID_2276077,Human_RBP_ID_3378039,Human_RBP_ID_4193144,Human_RBP_ID_5551383,Human_RBP_ID_6085827,Human_RBP_ID_8355733,Human_RBP_ID_9005358,Human_RBP_ID_9644798,Human_RBP_ID_11673528,Human_RBP_ID_17062244,Human_RBP_ID_17184682,Human_RBP_ID_18416923,Human_RBP_ID_18610790,Human_RBP_ID_19028318,Human_RBP_ID_19658845,Human_RBP_ID_22032794,Human_RBP_ID_22164846,Human_RBP_ID_22381211,Human_RBP_ID_22491572,Human_RBP_ID_22791553,Human_RBP_ID_22892800,Human_RBP_ID_23154620,Human_RBP_ID_23514555,Human_RBP_ID_24404073,Human_RBP_ID_24461744,Human_RBP_ID_24896919,Human_RBP_ID_26605322,Human_RBP_ID_26894545,Human_RBP_ID_27204926 116861 RMVar_ID_116861 Human_SNP_ID_812907804 m1A Human chr11 + 118397898 118397898 118397898 CCTCAAATCTAAGAGGGCTTCCCATCCTAGATATAAAATAGGTGTTGCCTATTGCTGTGCTTATA CCTCAAATCTAAGAGGGCTTCCCATCCTAGATGTAAAATAGGTGTTGCCTATTGCTGTGCTTATA A G UBE4A Ensembl:ENSG00000110344 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7108613 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_389784,Human_RBP_ID_4149037 Human_miRNA_ID_1349493 116862 RMVar_ID_116862 Human_SNP_ID_812935453 m1A Human chr11 - 64270249 64270162 64270249 CAGCTGGACGCGAGTCTTCCAGTCCTGGTGGGATCGGAACTTGGGCAGGGGAAGCTCCGCCCCCT CAGCTGGACGCGAGTCTTCCAGTCCTGGTGGG_________________________________ GCCCAGGGCAGTGGGAACGGGTGGAGTTTCGGGATGTGGAGCGAAGGTCACTGGGAGGGGGCGGAGCTTCCCCTGCCCAAGTTCCGAT G BAD Ensembl:ENSG00000002330 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:64270201..64270361 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..65 33 THCA 1 - Human_RBP_ID_399884 Human_Splice_Rec_1253262,Human_Splice_Rec_1253268,Human_Splice_Rec_1253270,Human_Splice_Rec_1253278,Human_Splice_Rec_1253280,Human_Splice_Rec_1253282 116863 RMVar_ID_116863 Human_SNP_ID_812939453 m1A Human chr11 + 117295206 117295206 117295206 TTGGAGCCGTTGATGAAGAACTTGTCTGATTCAGTGATGGCAGCAATGTTGGCACGCACAGTGAC TTGGAGCCGTTGATGAAGAACTTGTCTGATTCCGTGATGGCAGCAATGTTGGCACGCACAGTGAC A C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:117295156..117295501 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116864 RMVar_ID_116864 Human_SNP_ID_812952065 m1A Human chr11 + 57327465 57327465 57327465 AAGACTCGCCTCGGCCCCCTTCATATTCTTTCATGGCTTTTTCATAGTCCCTCCTGGCATCCTCA AAGACTCGCCTCGGCCCCCTTCATATTCTTTCGTGGCTTTTTCATAGTCCCTCCTGGCATCCTCA A G AP000781.1 Ensembl:ENSG00000254662 lincRNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:57327426..57327583 26863196 MeRIP-seq:(Medium) rs1188248956 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 116865 RMVar_ID_116865 Human_SNP_ID_812960316 m1A Human chr11 - 117229474 117229474 117229474 CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCATGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC CCGGCAGCAGGTGGAGGCTGTGTTGGCTGGGCGTGAAGCTGTGCGCTGGCACTCAGAGCAGAGGC T C PCSK7 Ensembl:ENSG00000160613 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:117229423..117229868 26863196 MeRIP-seq:(Medium) rs985732997 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach Human_RBP_ID_871184,Human_RBP_ID_6048039 Human_Splice_Rec_1301763,Human_Splice_Rec_1301815,Human_Splice_Rec_1301877 RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292,RMVar_hsa_circ_93304,RMVar_hsa_circ_153294,RMVar_hsa_circ_267555 116866 RMVar_ID_116866 Human_SNP_ID_812973941 m1A Human chr11 + 64237213 64237213 64237213 TTTCAGACCTAAAAAAAAGGACAGTGCTGTGAAGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG TTTCAGACCTAAAAAAAAGGACAGTGCTGTGACGCCAGACAGGTGAGTCTTTTGGACTCCAGCTG A C VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:64236304..64237600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,LICA,liver neoplasm,large_intestine adenocarcinoma 5 liver,large intestine Human_RBP_ID_987803 Human_Splice_Rec_1252926,Human_Splice_Rec_1252927,Human_Splice_Rec_1252938,Human_Splice_Rec_1252939,Human_Splice_Rec_1252943 Human_miRNA_ID_713622,Human_miRNA_ID_793151,Human_miRNA_ID_1515490 RMVar_hsa_circ_7888 116867 RMVar_ID_116867 Human_SNP_ID_812985997 m1A Human chr11 - 112025525 112025525 112025525 GTACCTCCTGCAAGGCCGTCCACCGAGCCTCGAGTCCCGCCCATGGGGCTACATTCTGAGCCCGT GTACCTCCTGCAAGGCCGTCCACCGAGCCTCGGGTCCCGCCCATGGGGCTACATTCTGAGCCCGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:112025474..112025589 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 2 pancreas 116868 RMVar_ID_116868 Human_SNP_ID_812993340 m1A Human chr11 + 39161718 39161718 39161718 AACCGCCGTGGTTGTGGGGACTATAAGGGATGATGTGCGGGTTCAGGAGGTGCCCAAACTGAAGG AACCGCCGTGGTTGTGGGGACTATAAGGGATGGTGTGCGGGTTCAGGAGGTGCCCAAACTGAAGG A G AC021723.1 Ensembl:ENSG00000240975 Pseudogene exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c chr11:39161623..39161814;chr11:39161700..39161829 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_miRNA_ID_1824099 116869 RMVar_ID_116869 Human_SNP_ID_813005985 m1A Human chr11 - 6320205 6320205 6320205 GCTGCTGGCCAAGGCGGAGCGCGTGAGCTCGCACGCCAACGCCGCCCAAGAGCGCGCGGTGCGCC GCTGCTGGCCAAGGCGGAGCGCGTGAGCTCGCGCGCCAACGCCGCCCAAGAGCGCGCGGTGCGCC T C CAVIN3 Ensembl:ENSG00000170955 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:6320155..6320401 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - RMVar_hsa_circ_126440,RMVar_hsa_circ_147817 116870 RMVar_ID_116870 Human_SNP_ID_813011476 m1A Human chr11 + 64236260 64236260 64236260 CCCCCCTGTTCTTCTCCTGAGCACAGATCCTCATGATCCGGTACCCGAGCAGTCAGCTGGGGGAG CCCCCCTGTTCTTCTCCTGAGCACAGATCCTCCTGATCCGGTACCCGAGCAGTCAGCTGGGGGAG A C VEGFB Ensembl:ENSG00000173511 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64234786..64237154 32194978 MeRIP-seq:(Medium) rs200892426 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_399815,Human_RBP_ID_867645,Human_RBP_ID_3940666,Human_RBP_ID_4168758 Human_Splice_Rec_1252924,Human_Splice_Rec_1252925,Human_Splice_Rec_1252936,Human_Splice_Rec_1252937 RMVar_hsa_circ_7888,RMVar_hsa_circ_150439,RMVar_hsa_circ_75723 116871 RMVar_ID_116871 Human_SNP_ID_813013033 m1A Human chr11 + 118657691 118657691 118657691 GAGGAGCGATGCAGTTGGGAGAGGAAGCTAGAAGGGTTATGGTTGGAGTTCTGTACAGTGTTGAG GAGGAGCGATGCAGTTGGGAGAGGAAGCTAGACGGGTTATGGTTGGAGTTCTGTACAGTGTTGAG A C PHLDB1 Ensembl:ENSG00000019144 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:118657641..118657753 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_390000 116872 RMVar_ID_116872 Human_SNP_ID_813024106 m1A Human chr11 - 112249042 112249042 112249042 TCCATCAGATTACCCTCCTTTCTCGAGTGCCCACCCACCACCCAACGGAGGTTCCGATGCCATTT TCCATCAGATTACCCTCCTTTCTCGAGTGCCCGCCCACCACCCAACGGAGGTTCCGATGCCATTT T C PLET1 Ensembl:ENSG00000188771 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:112249004..112249088 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 116873 RMVar_ID_116873 Human_SNP_ID_813026624 m1A Human chr11 - 3686194 3686194 3686194 GTGTATGTTGACTCTCAACACGTTCTTTGCAGACATTATGATCTCAACCAGCTGCTGGAGCCTCG GTGTATGTTGACTCTCAACACGTTCTTTGCAGGCATTATGATCTCAACCAGCTGCTGGAGCCTCG T C NUP98 Ensembl:ENSG00000110713 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:3686150..3693119 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_29994,Human_RBP_ID_11613319,Human_RBP_ID_22538006 Human_Splice_Rec_1201676,Human_Splice_Rec_1201740,Human_Splice_Rec_1201806,Human_Splice_Rec_1201892,Human_Splice_Rec_1201912 RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_333285,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_330576,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_147632,RMVar_hsa_circ_147633,RMVar_hsa_circ_338503,RMVar_hsa_circ_379094,RMVar_hsa_circ_320609,RMVar_hsa_circ_295579,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_147637,RMVar_hsa_circ_315993,RMVar_hsa_circ_319996,RMVar_hsa_circ_310270,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_5699,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_147642,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_318966,RMVar_hsa_circ_354108,RMVar_hsa_circ_290079,RMVar_hsa_circ_40644,RMVar_hsa_circ_147644,RMVar_hsa_circ_147645 116874 RMVar_ID_116874 Human_SNP_ID_813051743 m1A Human chr11 + 65582421 65582421 65582421 GAGACTGAGGTGGTAGGGTTGGAGGTGCTGGGAACCCAGGAGAAAGAAGTTGAGGGGTCAGGGTT GAGACTGAGGTGGTAGGGTTGGAGGTGCTGGGTACCCAGGAGAAAGAAGTTGAGGGGTCAGGGTT A T EHBP1L1 Ensembl:ENSG00000173442 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65581624..65583766 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_2601,Human_RBP_ID_5342658,Human_RBP_ID_8773711,Human_RBP_ID_9414207,Human_RBP_ID_18932603 RMVar_hsa_circ_12906,RMVar_hsa_circ_362176 116875 RMVar_ID_116875 Human_SNP_ID_813082778 m1A Human chr11 - 57742241 57742241 57742241 CGCGCCCCCCACTTCCCATTTCAAACCTCAGCATGAGGGCTTCTACCCAAATCTCCCTACGACAG CGCGCCCCCCACTTCCCATTTCAAACCTCAGCCTGAGGGCTTCTACCCAAATCTCCCTACGACAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:57742191..57742290 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate 116876 RMVar_ID_116876 Human_SNP_ID_813089218 m1A Human chr11 + 67586545 67586545 67586545 TCAAGGCCTTCCTGGCCTCCCCTGAGTACGTGAACCTCCCCATCAATGGCAACGGGAAACAGTGA TCAAGGCCTTCCTGGCCTCCCCTGAGTACGTGGACCTCCCCATCAATGGCAACGGGAAACAGTGA A G GSTP1 Ensembl:ENSG00000084207 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_402118,Human_RBP_ID_22435517,Human_RBP_ID_23517183,Human_RBP_ID_26803908,Human_RBP_ID_26895991,Human_RBP_ID_27206145 Human_miRNA_ID_2367272,Human_miRNA_ID_3015069 RMVar_hsa_circ_83436,RMVar_hsa_circ_109001,RMVar_hsa_circ_151079,RMVar_hsa_circ_93515,RMVar_hsa_circ_151080,RMVar_hsa_circ_92182,RMVar_hsa_circ_114794,RMVar_hsa_circ_151085,RMVar_hsa_circ_92949,RMVar_hsa_circ_151086,RMVar_hsa_circ_151087,RMVar_hsa_circ_97538,RMVar_hsa_circ_151089,RMVar_hsa_circ_151090 116877 RMVar_ID_116877 Human_SNP_ID_813090776 m1A Human chr11 + 574783 574783 574783 CGCCGCTGGCCCTCGGTGAGTCGCAGTGGCCCACCCTGCTGCACCCAGGCTCCCTCCCCCGCCTG CGCCGCTGGCCCTCGGTGAGTCGCAGTGGCCCCCCCTGCTGCACCCAGGCTCCCTCCCCCGCCTG A C lnc-PHRF1-1 RNACentral:URS00008BB238 lincRNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:574739..574870 26863196 MeRIP-seq:(Medium) rs907986005 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116878 RMVar_ID_116878 Human_SNP_ID_813093705 m1A Human chr11 - 64270235 64270235 64270235 TCTTCCAGTCCTGGTGGGATCGGAACTTGGGCAGGGGAAGCTCCGCCCCCTCCCAGTGACCTTCG TCTTCCAGTCCTGGTGGGATCGGAACTTGGGCGGGGGAAGCTCCGCCCCCTCCCAGTGACCTTCG T C BAD Ensembl:ENSG00000002330 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:64270187..64270359 26863196 MeRIP-seq:(Medium) rs1348660780 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_399884 Human_miRNA_ID_870812,Human_miRNA_ID_871837,Human_miRNA_ID_1231370 116879 RMVar_ID_116879 Human_SNP_ID_813103102 m1A Human chr11 + 122560004 122560004 122560004 ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAAGTCCCTGTTCAGGCGATGGCGTTTGTTTTTAG ATCAGACTTTTAATCTGAGGGTCCAGGGTTCAGGTCCCTGTTCAGGCGATGGCGTTTGTTTTTAG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 116880 RMVar_ID_116880 Human_SNP_ID_813107542 m1A Human chr11 - 62606131 62606131 62606131 CCTTGTGTCTCCGGAGGGACGGGACAGTGCTGAGTGGTGGCGGGCGGGACCGCCGGCTGGTACAG CCTTGTGTCTCCGGAGGGACGGGACAGTGCTGTGTGGTGGCGGGCGGGACCGCCGGCTGGTACAG T A EML3 Ensembl:ENSG00000149499 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:62606000..62606167 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_9275779,Human_RBP_ID_18973810,Human_RBP_ID_26318513,Human_RBP_ID_27836330 Human_Splice_Rec_1247940,Human_Splice_Rec_1247941,Human_Splice_Rec_1247980,Human_Splice_Rec_1247981,Human_Splice_Rec_1248022,Human_Splice_Rec_1248023,Human_Splice_Rec_1248041,Human_Splice_Rec_1248072,Human_Splice_Rec_1248073,Human_Splice_Rec_1248112,Human_Splice_Rec_1248113,Human_Splice_Rec_1248154,Human_Splice_Rec_1248155,Human_Splice_Rec_1248194,Human_Splice_Rec_1248195,Human_Splice_Rec_1248222,Human_Splice_Rec_1248223,Human_Splice_Rec_1248234,Human_Splice_Rec_1248235,Human_Splice_Rec_1248240,Human_Splice_Rec_1248244,Human_Splice_Rec_1248245 RMVar_hsa_circ_150201,RMVar_hsa_circ_43221,RMVar_hsa_circ_330752,RMVar_hsa_circ_150200,RMVar_hsa_circ_370031,RMVar_hsa_circ_83579,RMVar_hsa_circ_294932,RMVar_hsa_circ_150203,RMVar_hsa_circ_150204 116881 RMVar_ID_116881 Human_SNP_ID_813136674 m1A Human chr11 + 57320556 57320556 57320556 GCTTGCTGCCACCATAGGGCTGGGGTCCTGCCAGCATGTTCATCTTCCTGGCAGAAGGCAACTCA GCTTGCTGCCACCATAGGGCTGGGGTCCTGCCGGCATGTTCATCTTCCTGGCAGAAGGCAACTCA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:57320506..57320594 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 116882 RMVar_ID_116882 Human_SNP_ID_813144186 m1A Human chr11 - 10807379 10807379 10807379 GTCTAATTTTGGTGCTCTTTCTCGTTCCAGGTATTTCATTTCTCCTGTCCCCTCCCCTCCCCACC GTCTAATTTTGGTGCTCTTTCTCGTTCCAGGTTTTTCATTTCTCCTGTCCCCTCCCCTCCCCACC T A EIF4G2 Ensembl:ENSG00000110321 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:10807351..10807400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_5126237,Human_RBP_ID_5435985,Human_RBP_ID_5488969,Human_RBP_ID_6041169,Human_RBP_ID_17073649,Human_RBP_ID_17462752,Human_RBP_ID_18933333,Human_RBP_ID_22568676,Human_RBP_ID_22644075,Human_RBP_ID_24458680,Human_RBP_ID_24866794,Human_RBP_ID_27417271,Human_RBP_ID_27836292 Human_Splice_Rec_1210496,Human_Splice_Rec_1210606,Human_Splice_Rec_1210648,Human_Splice_Rec_1210722,Human_Splice_Rec_1210756,Human_Splice_Rec_1210782,Human_Splice_Rec_1210808,Human_Splice_Rec_1210809,Human_Splice_Rec_1210816,Human_Splice_Rec_1210817,Human_Splice_Rec_1210832,Human_Splice_Rec_1210842,Human_Splice_Rec_1210866,Human_Splice_Rec_1210880 Human_miRNA_ID_1231313 RMVar_hsa_circ_6954,RMVar_hsa_circ_84701,RMVar_hsa_circ_148193,RMVar_hsa_circ_46090,RMVar_hsa_circ_374422,RMVar_hsa_circ_148209,RMVar_hsa_circ_370220,RMVar_hsa_circ_148216,RMVar_hsa_circ_366770,RMVar_hsa_circ_15874 116883 RMVar_ID_116883 Human_SNP_ID_813160705 m1A Human chr11 - 8980930 8980930 8980930 GTCTCATTCCTTATTAGATGTCTATCTCAAATAACAGAGTTTGAAAAATATTGGTTTTATCATTT GTCTCATTCCTTATTAGATGTCTATCTCAAATGACAGAGTTTGAAAAATATTGGTTTTATCATTT T C NRIP3 Ensembl:ENSG00000175352 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs2568044 Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_79930,RMVar_hsa_circ_112229,RMVar_hsa_circ_124010,RMVar_hsa_circ_122236,RMVar_hsa_circ_95094,RMVar_hsa_circ_147981,RMVar_hsa_circ_147983,RMVar_hsa_circ_147984,RMVar_hsa_circ_147985,RMVar_hsa_circ_147982 116884 RMVar_ID_116884 Human_SNP_ID_813164238 m1A Human chr11 - 94545483 94545480 94545483 TCGTCCACGTGGATGAAGGCGCCGCGGGGCACAAAGCGCTCGTAGTTGGCACGGTCTGGGCCCAG TCGTCCACGTGGATGAAGGCGCCGCGGGGCAC___GCGCTCGTAGTTGGCACGGTCTGGGCCCAG CTTT C AP000943.2 Ensembl:ENSG00000255929 lincRNA exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:94545432..94545532 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..35 33 KIRP 1 - 116885 RMVar_ID_116885 Human_SNP_ID_813175788 m1A Human chr11 + 62831101 62831101 62831101 CCCGGCAGGACATGGTGTCGGGAGGGGGAGGGACGAGGGTCACTGGGGGGGGCAGAGGGGCGATG CCCGGCAGGACATGGTGTCGGGAGGGGGAGGGGCGAGGGTCACTGGGGGGGGCAGAGGGGCGATG A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62831051..62831275 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus 116886 RMVar_ID_116886 Human_SNP_ID_813179583 m1A Human chr11 + 32588650 32588650 32588650 TGGTATCCCTACTCTTGATCCTGGAACCAGACAAGCAAGAAGCTTTGATTGAAAGCCTATGTGAA TGGTATCCCTACTCTTGATCCTGGAACCAGACCAGCAAGAAGCTTTGATTGAAAGCCTATGTGAA A C EIF3M Ensembl:ENSG00000149100 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_749739,Human_RBP_ID_1456235,Human_RBP_ID_1778350,Human_RBP_ID_5436358,Human_RBP_ID_5489536,Human_RBP_ID_8349911,Human_RBP_ID_9362085,Human_RBP_ID_11597692,Human_RBP_ID_17804511,Human_RBP_ID_18606791,Human_RBP_ID_22434262,Human_RBP_ID_23113063,Human_RBP_ID_23206871,Human_RBP_ID_23501901,Human_RBP_ID_26804513 Human_Splice_Rec_1225802,Human_Splice_Rec_1225803,Human_Splice_Rec_1225812,Human_Splice_Rec_1225813,Human_Splice_Rec_1225832,Human_Splice_Rec_1225858,Human_Splice_Rec_1225859,Human_Splice_Rec_1225868,Human_Splice_Rec_1225869,Human_Splice_Rec_1225892,Human_Splice_Rec_1225893,Human_Splice_Rec_1225902,Human_Splice_Rec_1225906,Human_Splice_Rec_1225907 RMVar_hsa_circ_116593,RMVar_hsa_circ_7077,RMVar_hsa_circ_346550,RMVar_hsa_circ_42215,RMVar_hsa_circ_148860,RMVar_hsa_circ_272741,RMVar_hsa_circ_314065,RMVar_hsa_circ_355095,RMVar_hsa_circ_362842,RMVar_hsa_circ_329123,RMVar_hsa_circ_291381,RMVar_hsa_circ_42313,RMVar_hsa_circ_148858,RMVar_hsa_circ_148859,RMVar_hsa_circ_288887,RMVar_hsa_circ_148857,RMVar_hsa_circ_276145,RMVar_hsa_circ_148861,RMVar_hsa_circ_148862 116887 RMVar_ID_116887 Human_SNP_ID_813202817 m1A Human chr11 + 18402940 18402940 18402940 TGCAATCTGGATTCAGCCCGATTCCGTTACCTAATGGGGGAAAGGCTGGGAGTTCACCCATTAAG TGCAATCTGGATTCAGCCCGATTCCGTTACCTGATGGGGGAAAGGCTGGGAGTTCACCCATTAAG A G LDHA Ensembl:ENSG00000134333 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs4820 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_393417,Human_RBP_ID_4156073,Human_RBP_ID_8348261,Human_RBP_ID_9001787,Human_RBP_ID_17231652,Human_RBP_ID_23497776 Human_Splice_Rec_1218743,Human_Splice_Rec_1218757,Human_Splice_Rec_1218785,Human_Splice_Rec_1218791,Human_Splice_Rec_1218809,Human_Splice_Rec_1218823,Human_Splice_Rec_1218837,Human_Splice_Rec_1218863,Human_Splice_Rec_1218877,Human_Splice_Rec_1218889,Human_Splice_Rec_1218899,Human_Splice_Rec_1218909,Human_Splice_Rec_1218919,Human_Splice_Rec_1218923,Human_Splice_Rec_1218929 Human_miRNA_ID_2970526 Clinvar_Rec_176 RMVar_hsa_circ_37723,RMVar_hsa_circ_338133,RMVar_hsa_circ_148595,RMVar_hsa_circ_106856,RMVar_hsa_circ_270675,RMVar_hsa_circ_304781,RMVar_hsa_circ_108291,RMVar_hsa_circ_148596,RMVar_hsa_circ_96667,RMVar_hsa_circ_148594,RMVar_hsa_circ_299052,RMVar_hsa_circ_148597,RMVar_hsa_circ_148598 116888 RMVar_ID_116888 Human_SNP_ID_813208182 m1A Human chr11 - 64778457 64778457 64778457 CCGGCAGCGCATTCGGGTCCCCTCCCCCCGGGAGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAA CCGGCAGCGCATTCGGGTCCCCTCCCCCCGGGTGGCTTGCGAAGGAGAAGCCGCCGCAGAGGAAA T A SF1 Ensembl:ENSG00000168066 Protein coding 5'UTR GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEK293T,ALKBH3 KO;HTR8/Svneo,Hypoxia IP chr11:64778329..64778505;chr11:64778387..64778686 26863410,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_227921,Human_RBP_ID_400115,Human_RBP_ID_4185050,Human_RBP_ID_5460608,Human_RBP_ID_5490030,Human_RBP_ID_6084644,Human_RBP_ID_8770823,Human_RBP_ID_9275856,Human_RBP_ID_9363734,Human_RBP_ID_18416862,Human_RBP_ID_22895692,Human_RBP_ID_23512688,Human_RBP_ID_24542657 Human_Splice_Rec_1254785,Human_Splice_Rec_1254809,Human_Splice_Rec_1254833,Human_Splice_Rec_1254855,Human_Splice_Rec_1254879,Human_Splice_Rec_1254973,Human_Splice_Rec_1254979,Human_Splice_Rec_1254987,Human_Splice_Rec_1254999,Human_Splice_Rec_1255005 116889 RMVar_ID_116889 Human_SNP_ID_813217721 m1A Human chr11 + 66061941 66061941 66061941 CCCCCATGGCTGATTGCCATGCAGCGATATGGACCACCCCCATCGTATCCCAACCTGAAAATCCC CCCCCATGGCTGATTGCCATGCAGCGATATGGGCCACCCCCATCGTATCCCAACCTGAAAATCCC A G SF3B2 Ensembl:ENSG00000087365 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr11:66061863..66061940;chr11:66061876..66062000 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine Human_RBP_ID_29638,Human_RBP_ID_401214,Human_RBP_ID_865993,Human_RBP_ID_1459444,Human_RBP_ID_1781599,Human_RBP_ID_3378265,Human_RBP_ID_8356285,Human_RBP_ID_8771146,Human_RBP_ID_9254708,Human_RBP_ID_9275938,Human_RBP_ID_9362573,Human_RBP_ID_17799462,Human_RBP_ID_22433124,Human_RBP_ID_26317826,Human_RBP_ID_26895104,Human_RBP_ID_27414763,Human_RBP_ID_27803686 Human_Splice_Rec_1261510,Human_Splice_Rec_1261511,Human_Splice_Rec_1261552,Human_Splice_Rec_1261553,Human_Splice_Rec_1261648,Human_Splice_Rec_1261649 RMVar_hsa_circ_339833,RMVar_hsa_circ_150819,RMVar_hsa_circ_93752,RMVar_hsa_circ_54165,RMVar_hsa_circ_31861,RMVar_hsa_circ_67518,RMVar_hsa_circ_7266,RMVar_hsa_circ_290077,RMVar_hsa_circ_150820,RMVar_hsa_circ_267776,RMVar_hsa_circ_150821,RMVar_hsa_circ_150822 116890 RMVar_ID_116890 Human_SNP_ID_813218291 m1A Human chr11 - 57808213 57808213 57808213 CTAGGATGGCAGGAGTCTTGCTCTCCTTAAGAAGTGAGATGTATATCCGAACCACCTCTGGCTGA CTAGGATGGCAGGAGTCTTGCTCTCCTTAAGACGTGAGATGTATATCCGAACCACCTCTGGCTGA T G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57806981..57808313 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD 2 - 116891 RMVar_ID_116891 Human_SNP_ID_813231489 m1A Human chr11 - 77474208 77474208 77474208 CCGGAGCCGCAGCCGCCGCCGCCGCGCCGGGGAGGGGGAGTGGGGGAGGGGGAGGGGGAGAAGGG CCGGAGCCGCAGCCGCCGCCGCCGCGCCGGGGGGGGGGAGTGGGGGAGGGGGAGGGGGAGAAGGG T C PAK1 Ensembl:ENSG00000149269 Protein coding intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:77474115..77474309 26863196 MeRIP-seq:(Medium) rs1393779126 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_269423,Human_RBP_ID_5255890,Human_RBP_ID_8359475,Human_RBP_ID_11722155,Human_RBP_ID_17801656,Human_RBP_ID_22491836 116892 RMVar_ID_116892 Human_SNP_ID_813235246 m1A Human chr11 - 64243992 64243992 64243992 GCTCAGTTCGTCGCTCTATTTTGAGCAGCTCCACCTCGAACACCAGGGTTGCACCACCTGTAGGG GCTCAGTTCGTCGCTCTATTTTGAGCAGCTCCCCCTCGAACACCAGGGTTGCACCACCTGTAGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:64243826..64244132 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116893 RMVar_ID_116893 Human_SNP_ID_813246623 m1A Human chr11 - 6611274 6611274 6611274 TAGAATTCGGCTCATCTCCTTAGCTGCCCAGAAATTCATCTCAGATATTGCCAATGATGCCCTAC TAGAATTCGGCTCATCTCCTTAGCTGCCCAGACATTCATCTCAGATATTGCCAATGATGCCCTAC T G AC091564.7,TAF10 Ensembl:ENSG00000285338,Ensembl:ENSG00000166337 lincRNA,Protein coding exon,CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:6610926..6611467 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_18188164,Human_RBP_ID_26803178 Human_Splice_Rec_1205190,Human_Splice_Rec_1205191,Human_Splice_Rec_1205194,Human_Splice_Rec_1205195,Human_Splice_Rec_1205198,Human_Splice_Rec_1205199,Human_Splice_Rec_1205206,Human_Splice_Rec_1205226,Human_Splice_Rec_1205227 Human_miRNA_ID_2065293,Human_miRNA_ID_2132244,Human_miRNA_ID_2403923,Human_miRNA_ID_2703161,Human_miRNA_ID_2934469,Human_miRNA_ID_3153674,Human_miRNA_ID_3157538,Human_miRNA_ID_3173622,Human_miRNA_ID_3191170,Human_miRNA_ID_3205112 RMVar_hsa_circ_81150,RMVar_hsa_circ_99612,RMVar_hsa_circ_147882,RMVar_hsa_circ_147883,RMVar_hsa_circ_147884 116894 RMVar_ID_116894 Human_SNP_ID_813254000 m1A Human chr11 - 114400706 114400706 114400706 CGGTCACTTTCGTTTCAAGGTTGCCCACAAAGAGAGTGCGATCCGCTTCCGCCGCCGCCGCCCCC CGGTCACTTTCGTTTCAAGGTTGCCCACAAAGGGAGTGCGATCCGCTTCCGCCGCCGCCGCCCCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:114400659..114400740 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 8 liver 116895 RMVar_ID_116895 Human_SNP_ID_813259104 m1A Human chr11 + 63827033 63827033 63827033 CAGCCTCCTGCAAGACTGGTCCAGGCACCCCCAGGGCACCAAGCGTGTGGGAGCAGGTGACACCT CAGCCTCCTGCAAGACTGGTCCAGGCACCCCCGGGGCACCAAGCGTGTGGGAGCAGGTGACACCT A G SPINDOC Ensembl:ENSG00000168005 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:63826984..63827053 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809,RMVar_hsa_circ_81189,RMVar_hsa_circ_150379 116896 RMVar_ID_116896 Human_SNP_ID_813262464 m1A Human chr11 - 72827214 72827214 72827214 GATATGGTCCCCACACACCACGTCATTACAGTAGGAAAGGACATTGATGGTCCTGGAGCCTGGGG GATATGGTCCCCACACACCACGTCATTACAGTCGGAAAGGACATTGATGGTCCTGGAGCCTGGGG T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72827211..72828526 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_1265740 116897 RMVar_ID_116897 Human_SNP_ID_813268593 m1A Human chr11 - 119048797 119048797 119048797 GAGAAGAAGCAGAAGCCCGCCAGGAAGCGGCGAATGGTAGAGGAGATCGGGGTGGAGCTGGTTGT GAGAAGAAGCAGAAGCCCGCCAGGAAGCGGCGGATGGTAGAGGAGATCGGGGTGGAGCTGGTTGT T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:119048751..119048905 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_226707,Human_RBP_ID_871558,Human_RBP_ID_3939885,Human_RBP_ID_9254737,Human_RBP_ID_9276114,Human_RBP_ID_9363016,Human_RBP_ID_17649339,Human_RBP_ID_22433997,Human_RBP_ID_22755060,Human_RBP_ID_23489646,Human_RBP_ID_26317868,Human_RBP_ID_27804093 Human_Splice_Rec_1306264,Human_Splice_Rec_1306265,Human_Splice_Rec_1306358,Human_Splice_Rec_1306359,Human_Splice_Rec_1306408,Human_Splice_Rec_1306409,Human_Splice_Rec_1306494,Human_Splice_Rec_1306495,Human_Splice_Rec_1306513,Human_Splice_Rec_1306546,Human_Splice_Rec_1306547 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 116898 RMVar_ID_116898 Human_SNP_ID_813279755 m1A Human chr11 + 67443368 67443368 67443368 CAGCCCGGCCCCTGCAGCCCCGCCCAGCCCCCAGCCCGCGCCCCTAGCCCCGGCCCTGCCGCGCT CAGCCCGGCCCCTGCAGCCCCGCCCAGCCCCCGGCCCGCGCCCCTAGCCCCGGCCCTGCCGCGCT A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:67443358..67443475 26863410 MeRIP-seq:(Medium) rs1335561019 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 116899 RMVar_ID_116899 Human_SNP_ID_813295666 m1A Human chr11 - 65617351 65617351 65617351 ACAGGAGGACAAGCTGAGGTCCAGGCCCACTCACCGAGACCTGGTTGAAGCCAAACACAGAGTGC ACAGGAGGACAAGCTGAGGTCCAGGCCCACTCGCCGAGACCTGGTTGAAGCCAAACACAGAGTGC T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:65617316..65618069 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 116900 RMVar_ID_116900 Human_SNP_ID_813316843 m1A Human chr11 - 64246515 64246515 64246515 GGGGCGGACGATGAGGGCCCAGTGAGGCGCCAAGGGAAGGTCACCGTCAAGTATGACCGCAAGGA GGGGCGGACGATGAGGGCCCAGTGAGGCGCCAGGGGAAGGTCACCGTCAAGTATGACCGCAAGGA T C PPP1R14B Ensembl:ENSG00000173457 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:64246496..64246900 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_399851 Human_Splice_Rec_1253045 Human_miRNA_ID_2217949 RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445 116901 RMVar_ID_116901 Human_SNP_ID_813320339 m1A Human chr11 + 63590176 63590175 63590176 GCTCGCAGTTCTCACTGGTCAGCTTGTAGAGCACCTCCTGCCCCACCAGCTCCTCCGCCCGCTGG GCTCGCAGTTCTCACTGGTCAGCTTGTAGAGC_CCTCCTGCCCCACCAGCTCCTCCGCCCGCTGG CA C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:63590126..63608492 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 READ 1 - 116902 RMVar_ID_116902 Human_SNP_ID_813325689 m1A Human chr11 + 407110 407110 407110 ACCAGGCCCGGCTCAGGAAGGCGTCCGAAAGCACCACGATGAGGCGTCGGCAGCGGCTCAGGTTC ACCAGGCCCGGCTCAGGAAGGCGTCCGAAAGCGCCACGATGAGGCGTCGGCAGCGGCTCAGGTTC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr11:406770..407164;chr11:406778..407114;chr11:406764..407164 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine 116903 RMVar_ID_116903 Human_SNP_ID_813338130 m1A Human chr11 - 812833 812833 812833 AAAGGCTTTATTTGCAGGGGAGCAGGAATTTAATCAAAAAGGCCAAATCCCATGTCATCATCTGA AAAGGCTTTATTTGCAGGGGAGCAGGAATTTATTCAAAAAGGCCAAATCCCATGTCATCATCTGA T A - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:812801..812875 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 2 stomach 116904 RMVar_ID_116904 Human_SNP_ID_813352575 m1A Human chr11 - 66285760 66285760 66285760 GCCAAGCTGATGGCATCTCTCTGGCACTTGGCAGCGATGGCCTTCATTACTTACGTGCTCCTGGC GCCAAGCTGATGGCATCTCTCTGGCACTTGGCTGCGATGGCCTTCATTACTTACGTGCTCCTGGC T A YIF1A Ensembl:ENSG00000174851 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:66285701..66285775 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_Splice_Rec_1262107,Human_Splice_Rec_1262117,Human_Splice_Rec_1262129,Human_Splice_Rec_1262143,Human_Splice_Rec_1262159,Human_Splice_Rec_1262169 RMVar_hsa_circ_43495,RMVar_hsa_circ_113317,RMVar_hsa_circ_120267,RMVar_hsa_circ_114475,RMVar_hsa_circ_98504,RMVar_hsa_circ_150870,RMVar_hsa_circ_150872,RMVar_hsa_circ_150873,RMVar_hsa_circ_150871,RMVar_hsa_circ_56571 116905 RMVar_ID_116905 Human_SNP_ID_813356304 m1A Human chr11 - 72005315 72005315 72005315 CACTTGCCAGGATGAGCCTGAGCAGCTGGATGACTGGAACCGCATTGCAGAGCTGCAGCAGCGCA CACTTGCCAGGATGAGCCTGAGCAGCTGGATGGCTGGAACCGCATTGCAGAGCTGCAGCAGCGCA T C NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:72004010..72007687 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 8 kidney Human_RBP_ID_1782353,Human_RBP_ID_3379528,Human_RBP_ID_6091597,Human_RBP_ID_8771601,Human_RBP_ID_9275113,Human_RBP_ID_18433159,Human_RBP_ID_18974599,Human_RBP_ID_22641822 Human_Splice_Rec_1272198,Human_Splice_Rec_1272199,Human_Splice_Rec_1272222,Human_Splice_Rec_1272223,Human_Splice_Rec_1272270,Human_Splice_Rec_1272271,Human_Splice_Rec_1272322,Human_Splice_Rec_1272323,Human_Splice_Rec_1272374,Human_Splice_Rec_1272375,Human_Splice_Rec_1272420,Human_Splice_Rec_1272421,Human_Splice_Rec_1272468,Human_Splice_Rec_1272469,Human_Splice_Rec_1272514,Human_Splice_Rec_1272515,Human_Splice_Rec_1272528,Human_Splice_Rec_1272540 Human_miRNA_ID_2395471 RMVar_hsa_circ_36724,RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494,RMVar_hsa_circ_377034 116906 RMVar_ID_116906 Human_SNP_ID_813360739 m1A Human chr11 - 67586499 67586499 67586499 GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCACTGAGGCGCCCCACATATGCTGAGAGCAGGGG GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCCCTGAGGCGCCCCACATATGCTGAGAGCAGGGG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67586456..67586582 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_151088 116907 RMVar_ID_116907 Human_SNP_ID_813360743 m1A Human chr11 - 67586499 67586499 67586499 GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCACTGAGGCGCCCCACATATGCTGAGAGCAGGGG GAGGCCAGGAAGGCCTTGAGCTTGGGCCGGGCGCTGAGGCGCCCCACATATGCTGAGAGCAGGGG T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:67586456..67586582 26863196 MeRIP-seq:(Medium) rs4891 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,colon adenocarcinoma,pancreas ductal_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 16 pancreas,large intestine,haematopoietic and lymphoid tissue GWAS_ID_6712,GWAS_ID_6713,GWAS_ID_6714,GWAS_ID_6715,GWAS_ID_6716,GWAS_ID_6717,GWAS_ID_6718,GWAS_ID_6719 RMVar_hsa_circ_151088 116908 RMVar_ID_116908 Human_SNP_ID_813367996 m1A Human chr11 + 69642094 69642094 69642094 TAAGGGCCGCGCGGCTGCCGGGAGCCCGCGGGAGGGGCGCAGGGACGCGGCATGGGTAGTTTTGG TAAGGGCCGCGCGGCTGCCGGGAGCCCGCGGGGGGGGCGCAGGGACGCGGCATGGGTAGTTTTGG A G CCND1 Ensembl:ENSG00000110092 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:69642086..69642256 26863196 MeRIP-seq:(Medium) rs1047557668 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_84086,RMVar_hsa_circ_151346 116909 RMVar_ID_116909 Human_SNP_ID_813369546 m1A Human chr11 + 3824043 3824043 3824043 CTACCTCAGCTGCACCTCCCCGTGTTCCTGCTATCGCCCGCTCTGCCGCCTCAACTTCGGCCTCA CTACCTCAGCTGCACCTCCCCGTGTTCCTGCTGTCGCCCGCTCTGCCGCCTCAACTTCGGCCTCA A G PGAP2 Ensembl:ENSG00000148985 Protein coding 3'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr11:3823861..3824303 26863196 MeRIP-seq:(Medium) rs185342002 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_9321271,Human_RBP_ID_17349967 Human_Splice_Rec_1202053,Human_Splice_Rec_1202065,Human_Splice_Rec_1202077,Human_Splice_Rec_1202095,Human_Splice_Rec_1202121,Human_Splice_Rec_1202133,Human_Splice_Rec_1202139,Human_Splice_Rec_1202151,Human_Splice_Rec_1202161,Human_Splice_Rec_1202175,Human_Splice_Rec_1202217,Human_Splice_Rec_1202235,Human_Splice_Rec_1202249,Human_Splice_Rec_1202261,Human_Splice_Rec_1202281,Human_Splice_Rec_1202295,Human_Splice_Rec_1202305,Human_Splice_Rec_1202319,Human_Splice_Rec_1202325,Human_Splice_Rec_1202335,Human_Splice_Rec_1202343,Human_Splice_Rec_1202353,Human_Splice_Rec_1202369 Human_miRNA_ID_1183023 RMVar_hsa_circ_107193,RMVar_hsa_circ_147732 116910 RMVar_ID_116910 Human_SNP_ID_813372787 m1A Human chr11 - 67490451 67490451 67490451 CCGGCAGCCCAGGGCCCGGTGCTCACCGTCGTACTTGTTGAGGATGGAAGAGCAGTGGTCCAGCA CCGGCAGCCCAGGGCCCGGTGCTCACCGTCGTGCTTGTTGAGGATGGAAGAGCAGTGGTCCAGCA T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr11:67490301..67490475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 116911 RMVar_ID_116911 Human_SNP_ID_813387144 m1A Human chr11 + 10508275 10508275 10508275 TTAAGGAACAAGTGATTATGCTACCTTTGCACAGTTAGGGTACCGCGGCCGTTAAACGCATGTCA TTAAGGAACAAGTGATTATGCTACCTTTGCACGGTTAGGGTACCGCGGCCGTTAAACGCATGTCA A G lnc-AMPD3-3 RNACentral:URS00008BDE77 lincRNA intron GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA Glucose starvation 4h chr11:10508049..10508398;chr11:10508042..10508369 26863196 MeRIP-seq:(Medium) rs7350542 Functional Loss SNV ICGC 33..33 33 COCA 2 - 116912 RMVar_ID_116912 Human_SNP_ID_813417484 m1A Human chr11 + 829510 829510 829510 GGAAGAGGAGGAGCGATTCCACACTGTGCTGGAGCAGCTGGGGGTGGCCCCGGTCCTGGGCAAGT GGAAGAGGAGGAGCGATTCCACACTGTGCTGGGGCAGCTGGGGGTGGCCCCGGTCCTGGGCAAGT A G CRACR2B Ensembl:ENSG00000177685 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:829477..829550 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_5111006,Human_RBP_ID_18973169,Human_RBP_ID_21965097 Human_Splice_Rec_1195807,Human_Splice_Rec_1195821,Human_Splice_Rec_1195837,Human_Splice_Rec_1195851,Human_Splice_Rec_1195859 116913 RMVar_ID_116913 Human_SNP_ID_813419405 m1A Human chr11 + 3828064 3828064 3828064 ACGGTGGGGATGTACTCTTTGGGGAAAGCGTTAGTTGTGTAGCAGATGAGCAGGCACGTCTTGCC ACGGTGGGGATGTACTCTTTGGGGAAAGCGTTGGTTGTGTAGCAGATGAGCAGGCACGTCTTGCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:3827677..3830536 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 116914 RMVar_ID_116914 Human_SNP_ID_813439246 m1A Human chr11 + 75572121 75572121 75572121 CAGGGTGCACACAGGATGGCAGGAGGCATCCAAAGGCTCCTGAGACACATGGGTGCTATTGGGGT CAGGGTGCACACAGGATGGCAGGAGGCATCCAGAGGCTCCTGAGACACATGGGTGCTATTGGGGT A G SERPINH1 Ensembl:ENSG00000149257 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:75572071..75572258 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_403860,Human_RBP_ID_17350298,Human_RBP_ID_22434756,Human_RBP_ID_23521569 116915 RMVar_ID_116915 Human_SNP_ID_813453253 m1A Human chr11 - 64246714 64246714 64246714 CCAGCCGGCGGGCGTCCCGGAGGCGGTGGCGCAGGGAGGGGCCCGACGCTCGCACGTGGCCCCGG CCAGCCGGCGGGCGTCCCGGAGGCGGTGGCGCGGGGAGGGGCCCGACGCTCGCACGTGGCCCCGG T C PPP1R14B Ensembl:ENSG00000173457 Protein coding 5'UTR GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:64246574..64246950 26863196 MeRIP-seq:(Medium) rs1160724369 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_227076,Human_RBP_ID_399855,Human_RBP_ID_750433,Human_RBP_ID_807854,Human_RBP_ID_4168843,Human_RBP_ID_5110479,Human_RBP_ID_5235231,Human_RBP_ID_5461148,Human_RBP_ID_8774331,Human_RBP_ID_9322132,Human_RBP_ID_17649671,Human_RBP_ID_22433714,Human_RBP_ID_22569393 Human_miRNA_ID_2295586 RMVar_hsa_circ_87118,RMVar_hsa_circ_106955,RMVar_hsa_circ_150440,RMVar_hsa_circ_150445 116916 RMVar_ID_116916 Human_SNP_ID_813453385 m1A Human chr11 + 66492824 66492824 66492824 GGAGCTGCCCTGGCCCCCAACCTTTGAGAAGGACAAGTTCCTCACCCCTGACTTCACCTCCCTGG GGAGCTGCCCTGGCCCCCAACCTTTGAGAAGGGCAAGTTCCTCACCCCTGACTTCACCTCCCTGG A G DPP3 Ensembl:ENSG00000254986 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:66492773..66492862 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_8356549 Human_Splice_Rec_1262761,Human_Splice_Rec_1262795,Human_Splice_Rec_1262829,Human_Splice_Rec_1262887,Human_Splice_Rec_1262935,Human_Splice_Rec_1262945,Human_Splice_Rec_1262955,Human_Splice_Rec_1262965 Human_miRNA_ID_2254957,Human_miRNA_ID_2254958 RMVar_hsa_circ_266471,RMVar_hsa_circ_49300,RMVar_hsa_circ_109976,RMVar_hsa_circ_52997,RMVar_hsa_circ_150893,RMVar_hsa_circ_111897,RMVar_hsa_circ_150896 116917 RMVar_ID_116917 Human_SNP_ID_813456540 m1A Human chr11 + 36422323 36422323 36422323 TTCAGGAGGGAAAGTCAGGAGGAACTCCAGAAAGTGTGTTCCTCCAGTAAAGGGGCAGAAGGAAG TTCAGGAGGGAAAGTCAGGAGGAACTCCAGAAGGTGTGTTCCTCCAGTAAAGGGGCAGAAGGAAG A G PRR5L Ensembl:ENSG00000135362 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:36422281..36422438 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_315452,RMVar_hsa_circ_323206,RMVar_hsa_circ_311045,RMVar_hsa_circ_69500 116918 RMVar_ID_116918 Human_SNP_ID_813465335 m1A Human chr11 - 8730051 8730051 8730051 AAGAGTAAGCCCAGTAATGGTCTACCTCCTTCACCCACACCTGCTGCTCCACCTCCCTTGCCCTC AAGAGTAAGCCCAGTAATGGTCTACCTCCTTCCCCCACACCTGCTGCTCCACCTCCCTTGCCCTC T G DENND2B Ensembl:ENSG00000166444 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:8730000..8730194 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach diffuse_adenocarcinoma 5 stomach Human_RBP_ID_27416807 Human_miRNA_ID_596260,Human_miRNA_ID_1237539,Human_miRNA_ID_1453310,Human_miRNA_ID_2100401,Human_miRNA_ID_2106349,Human_miRNA_ID_2112290,Human_miRNA_ID_2164843,Human_miRNA_ID_2221831,Human_miRNA_ID_2484887,Human_miRNA_ID_2596077,Human_miRNA_ID_2738998,Human_miRNA_ID_3039592,Human_miRNA_ID_3073263 RMVar_hsa_circ_114,RMVar_hsa_circ_108070,RMVar_hsa_circ_147957,RMVar_hsa_circ_81067,RMVar_hsa_circ_80502,RMVar_hsa_circ_147962,RMVar_hsa_circ_75978,RMVar_hsa_circ_147965,RMVar_hsa_circ_124340,RMVar_hsa_circ_147966,RMVar_hsa_circ_314841,RMVar_hsa_circ_147967,RMVar_hsa_circ_341464,RMVar_hsa_circ_14271,RMVar_hsa_circ_147968 116919 RMVar_ID_116919 Human_SNP_ID_813471134 m1A Human chr11 + 2885113 2885113 2885113 GCAGCTGCTCCGGCGCCTCCTCGAGGCCGTCGAGGGACTCAGCGGCCGGCTCGAGGGGCGGGCTG GCAGCTGCTCCGGCGCCTCCTCGAGGCCGTCGGGGGACTCAGCGGCCGGCTCGAGGGGCGGGCTG A G NONHSAG007437.2 RNACentral:URS00008B3B90 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:2885063..2885165 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 CESC 1 - 116920 RMVar_ID_116920 Human_SNP_ID_813498973 m1A Human chr11 + 60931883 60931883 60931883 GCGGGACATCAGAGCCCTTATCCCACTGGCCAAGGTAAGGAGACCTCCATCTCTGCCTGGGAAGG GCGGGACATCAGAGCCCTTATCCCACTGGCCATGGTAAGGAGACCTCCATCTCTGCCTGGGAAGG A T TMEM132A Ensembl:ENSG00000006118 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:60930516..60931892 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_18971983 Human_Splice_Rec_1244297,Human_Splice_Rec_1244317,Human_Splice_Rec_1244343,Human_Splice_Rec_1244355 RMVar_hsa_circ_26971,RMVar_hsa_circ_91410,RMVar_hsa_circ_149896 116921 RMVar_ID_116921 Human_SNP_ID_813503379 m1A Human chr11 + 111809772 111809772 111809772 AATCCACTAAATAATGGCATTTACTGATATCAATCTGAAATGGAGAAAGGCCAACTCTTCATTAG AATCCACTAAATAATGGCATTTACTGATATCACTCTGAAATGGAGAAAGGCCAACTCTTCATTAG A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:111809676..111809799 26863196 MeRIP-seq:(Medium) rs12575909 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue 116922 RMVar_ID_116922 Human_SNP_ID_813505399 m1A Human chr11 - 66340780 66340780 66340780 GGCTGGAGGAGGACCGCCAGAGCCTGGACCTCAGCTCTGGTAAGCGCGAGAGCCTGGGCACCCCG GGCTGGAGGAGGACCGCCAGAGCCTGGACCTCCGCTCTGGTAAGCGCGAGAGCCTGGGCACCCCG T G BRMS1 Ensembl:ENSG00000174744 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66340776..66340825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_18972330,Human_RBP_ID_19052335,Human_RBP_ID_22895425 Human_Splice_Rec_1262290,Human_Splice_Rec_1262291,Human_Splice_Rec_1262306,Human_Splice_Rec_1262307,Human_Splice_Rec_1262322,Human_Splice_Rec_1262323,Human_Splice_Rec_1262340,Human_Splice_Rec_1262341,Human_Splice_Rec_1262356,Human_Splice_Rec_1262357,Human_Splice_Rec_1262372,Human_Splice_Rec_1262373 RMVar_hsa_circ_2458,RMVar_hsa_circ_102545,RMVar_hsa_circ_150876,RMVar_hsa_circ_371832,RMVar_hsa_circ_150879 116923 RMVar_ID_116923 Human_SNP_ID_813516032 m1A Human chr11 - 102241420 102241420 102241420 CTACTTGTTGTCCTTCTCTCCCACACCTAGGCAGTTCCAAGCCTGAGCCTTTTCTCTCCCACTGC CTACTTGTTGTCCTTCTCTCCCACACCTAGGCTGTTCCAAGCCTGAGCCTTTTCTCTCCCACTGC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:102241370..102241474 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116924 RMVar_ID_116924 Human_SNP_ID_813525933 m1A Human chr11 + 94111710 94111710 94111710 TATCTTTTTCACAGAACGACCTGGCAAAGAGCAGCTCTATTTCTTTGGCAAGAATCTGGGTCCAA TATCTTTTTCACAGAACGACCTGGCAAAGAGCGGCTCTATTTCTTTGGCAAGAATCTGGGTCCAA A G HEPHL1 Ensembl:ENSG00000181333 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr11:94111666..94111753 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_Splice_Rec_1288706 116925 RMVar_ID_116925 Human_SNP_ID_813538384 m1A Human chr11 + 64318305 64318305 64318305 GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCTAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG A T PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64318151..64318471 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_227603,Human_RBP_ID_3940680,Human_RBP_ID_4185045,Human_RBP_ID_5314252,Human_RBP_ID_9322142 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 116926 RMVar_ID_116926 Human_SNP_ID_813538392 m1A Human chr11 + 64318305 64318305 64318305 GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCAAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG GGGGCCGGCGGTCAGTCTGCGGCAGCGGCAGCGAGACGGTACAGTGAAGGAGAGTGGGCGTCTGG A G PRDX5 Ensembl:ENSG00000126432 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr11:64318151..64318471 26863196 MeRIP-seq:(Medium) rs1301691525 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_227603,Human_RBP_ID_3940680,Human_RBP_ID_4185045,Human_RBP_ID_5314252,Human_RBP_ID_9322142 Human_Splice_Rec_1253613,Human_Splice_Rec_1253623,Human_Splice_Rec_1253631 116927 RMVar_ID_116927 Human_SNP_ID_813538589 m1A Human chr11 - 800076 800068 800077 GGGCGGGGCAGGACCGAGGCCCAGGGGTGACCAGGGTGACATGGTGGAGTTGGGGGTGGAGCCCA GGGCGGGGCAGGACCGAGGCCCAGGGGTGAC_________ATGGTGGAGTTGGGGGTGGAGCCCA TGTCACCCTG T PIDD1 Ensembl:ENSG00000177595 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:800025..800192 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..40 33 COAD 1 - Human_RBP_ID_3938804,Human_RBP_ID_5341125,Human_RBP_ID_18971604,Human_RBP_ID_19048925,Human_RBP_ID_22414418,Human_RBP_ID_22642220,Human_RBP_ID_22736193,Human_RBP_ID_26317974 116928 RMVar_ID_116928 Human_SNP_ID_813541640 m1A Human chr11 - 62671957 62671957 62671957 CCTCCTCCCTGCTCCTTGGGTCCTGCAGTGGCATCTCCTGAGGGCAGGAAGGGGAGTTCGCAGGA CCTCCTCCCTGCTCCTTGGGTCCTGCAGTGGCGTCTCCTGAGGGCAGGAAGGGGAGTTCGCAGGA T C LBHD1 Ensembl:ENSG00000162194 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA Glucose starvation 4h;HTR8/Svneo,Hypoxia IP chr11:62671676..62672330;chr11:62671676..62672350;chr11:62671701..62672439 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_22034544 116929 RMVar_ID_116929 Human_SNP_ID_813547017 m1A Human chr11 + 119048028 119048028 119048028 GTTCGGGCCACTTCTTGCGCTCCTCTACCCGAAAAAACAGCCCTTGGCACAGCTTCCTCAGCTCA GTTCGGGCCACTTCTTGCGCTCCTCTACCCGACAAAACAGCCCTTGGCACAGCTTCCTCAGCTCA A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:119047951..119048100 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 116930 RMVar_ID_116930 Human_SNP_ID_813564533 m1A Human chr11 - 129948421 129948414 129948421 GAGGCATCAAAGGCGGTTCACTGGGAAACTGGAATGTGGTAGGATTTAGAAGGTGGCTGAGGAAA GAGGCATCAAAGGCGGTTCACTGGGAAACTGG_______TAGGATTTAGAAGGTGGCTGAGGAAA ACCACATT A PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:129948414..129948552 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..39 33 PRAD 1 - Human_RBP_ID_6055364 RMVar_hsa_circ_20464,RMVar_hsa_circ_109588,RMVar_hsa_circ_35454,RMVar_hsa_circ_154020,RMVar_hsa_circ_265037,RMVar_hsa_circ_107893,RMVar_hsa_circ_154024,RMVar_hsa_circ_43703,RMVar_hsa_circ_98624,RMVar_hsa_circ_4479,RMVar_hsa_circ_316780,RMVar_hsa_circ_154027,RMVar_hsa_circ_351405,RMVar_hsa_circ_154029,RMVar_hsa_circ_369981,RMVar_hsa_circ_154031,RMVar_hsa_circ_154030,RMVar_hsa_circ_325747 116931 RMVar_ID_116931 Human_SNP_ID_813567301 m1A Human chr11 - 65590541 65590540 65590541 GCCTCCGGATGAGAGCGTTCTTCTTGTTGACCAGGGTGAACCACTCCTGGATCAGCACCTCCTCC GCCTCCGGATGAGAGCGTTCTTCTTGTTGACC_GGGTGAACCACTCCTGGATCAGCACCTCCTCC CT C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:65590467..65590577 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUAD 1 - 116932 RMVar_ID_116932 Human_SNP_ID_813581469 m1A Human chr11 - 119311423 119311423 119311423 CATCCCCTGAGCTGCCTCCTTCCTTTCCTCGCAGGCAAGTGAACAAGACCAAGATCCACAGCGAG CATCCCCTGAGCTGCCTCCTTCCTTTCCTCGCTGGCAAGTGAACAAGACCAAGATCCACAGCGAG T A MCAM Ensembl:ENSG00000076706 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated chr11:119311305..119311447;chr11:119311376..119311650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 1 oesophagus RMVar_hsa_circ_98748,RMVar_hsa_circ_116554,RMVar_hsa_circ_113856,RMVar_hsa_circ_153540,RMVar_hsa_circ_153541,RMVar_hsa_circ_122983,RMVar_hsa_circ_153543,RMVar_hsa_circ_82682,RMVar_hsa_circ_153544,RMVar_hsa_circ_153546,RMVar_hsa_circ_106467,RMVar_hsa_circ_153545 116933 RMVar_ID_116933 Human_SNP_ID_813616314 m1A Human chr11 + 114444553 114444553 114444553 CTGGGGATTCTCTCTTGCAGTCTGGCCTTACCAAGGCAGTGAAGGAGAGTACAATTACATTGCAG CTGGGGATTCTCTCTTGCAGTCTGGCCTTACCCAGGCAGTGAAGGAGAGTACAATTACATTGCAG A C REXO2 Ensembl:ENSG00000076043 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:114444551..114444575 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_748986,Human_RBP_ID_5086872,Human_RBP_ID_17804791,Human_RBP_ID_22643841,Human_RBP_ID_24557310,Human_RBP_ID_26768174,Human_RBP_ID_26775976 Human_Splice_Rec_1300186,Human_Splice_Rec_1300187,Human_Splice_Rec_1300206,Human_Splice_Rec_1300207,Human_Splice_Rec_1300219,Human_Splice_Rec_1300260,Human_Splice_Rec_1300261,Human_Splice_Rec_1300276,Human_Splice_Rec_1300277,Human_Splice_Rec_1300298,Human_Splice_Rec_1300299,Human_Splice_Rec_1300305 RMVar_hsa_circ_112275,RMVar_hsa_circ_153187,RMVar_hsa_circ_153189,RMVar_hsa_circ_286307,RMVar_hsa_circ_24815,RMVar_hsa_circ_375136,RMVar_hsa_circ_378725,RMVar_hsa_circ_19066,RMVar_hsa_circ_122083,RMVar_hsa_circ_153190,RMVar_hsa_circ_153191,RMVar_hsa_circ_33749,RMVar_hsa_circ_86783,RMVar_hsa_circ_153192 116934 RMVar_ID_116934 Human_SNP_ID_813632169 m1A Human chr11 + 118401673 118401673 118401673 GCGACGGACTCTCCATTCCAGAACCATGGCCCAATTTGTCCGTAACCTTGTGGAGAAGACCCCGG GCGACGGACTCTCCATTCCAGAACCATGGCCCGATTTGTCCGTAACCTTGTGGAGAAGACCCCGG A G AP001267.5,ATP5MG Ensembl:ENSG00000285827,Ensembl:ENSG00000167283 Protein coding,Protein coding CDS,CDS GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,mRNA Glucose starvation 4h chr11:118401601..118401725;chr11:118401601..118401828 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney Human_RBP_ID_32515,Human_RBP_ID_389814,Human_RBP_ID_1454408,Human_RBP_ID_1775898,Human_RBP_ID_3369296,Human_RBP_ID_4149082,Human_RBP_ID_5313838,Human_RBP_ID_9321787,Human_RBP_ID_18603633,Human_RBP_ID_22433981,Human_RBP_ID_22531430,Human_RBP_ID_23488902 Human_Splice_Rec_1304069,Human_Splice_Rec_1304073,Human_Splice_Rec_1304085,Human_Splice_Rec_1304089,Human_Splice_Rec_1304095,Human_Splice_Rec_1304103,Human_Splice_Rec_1304107,Human_Splice_Rec_1304111,Human_Splice_Rec_1304115 116935 RMVar_ID_116935 Human_SNP_ID_813638442 m1A Human chr11 + 60924722 60924722 60924722 CTGGCTCTGCCTCCTGGTGGCCCTCGCCCTGGACGTCGTGAGAGGTCAGCGGGAGGGGAGGGCCG CTGGCTCTGCCTCCTGGTGGCCCTCGCCCTGGTCGTCGTGAGAGGTCAGCGGGAGGGGAGGGCCG A T TMEM132A Ensembl:ENSG00000006118 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:60924611..60925236 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_867468,Human_RBP_ID_4184065,Human_RBP_ID_19049419 Human_Splice_Rec_1244277,Human_Splice_Rec_1244287,Human_Splice_Rec_1244307,Human_Splice_Rec_1244327,Human_Splice_Rec_1244329 116936 RMVar_ID_116936 Human_SNP_ID_813638453 m1A Human chr11 + 60924722 60924722 60924722 CTGGCTCTGCCTCCTGGTGGCCCTCGCCCTGGACGTCGTGAGAGGTCAGCGGGAGGGGAGGGCCG CTGGCTCTGCCTCCTGGTGGCCCTCGCCCTGGGCGTCGTGAGAGGTCAGCGGGAGGGGAGGGCCG A G TMEM132A Ensembl:ENSG00000006118 Protein coding exon GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:60924611..60925236 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 2 lung Human_RBP_ID_867468,Human_RBP_ID_4184065,Human_RBP_ID_19049419 Human_Splice_Rec_1244277,Human_Splice_Rec_1244287,Human_Splice_Rec_1244307,Human_Splice_Rec_1244327,Human_Splice_Rec_1244329 116937 RMVar_ID_116937 Human_SNP_ID_813650436 m1A Human chr11 - 74964972 74964972 74964972 AAGAAACCTGGCCTCTTACTGAAAGTAAAATGAACCATTTTTTAAGAGCATCCCTCATGCACATA AAGAAACCTGGCCTCTTACTGAAAGTAAAATGTACCATTTTTTAAGAGCATCCCTCATGCACATA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:74964969..74965075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 4 caecum,large intestine 116938 RMVar_ID_116938 Human_SNP_ID_813665033 m1A Human chr11 + 65503812 65503812 65503812 AGAACGAATGTAACTTTAAGGCAGGAAAGACAAATTTTATTCTTCATAAAGTGATGAGCATATAA AGAACGAATGTAACTTTAAGGCAGGAAAGACAGATTTTATTCTTCATAAAGTGATGAGCATATAA A G MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:65503761..65504057 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_294051,Human_RBP_ID_400787,Human_RBP_ID_1079279,Human_RBP_ID_1126467,Human_RBP_ID_1459230,Human_RBP_ID_1781471,Human_RBP_ID_2276112,Human_RBP_ID_3378080,Human_RBP_ID_5169384,Human_RBP_ID_5551387,Human_RBP_ID_6086139,Human_RBP_ID_8062096,Human_RBP_ID_9005397,Human_RBP_ID_9644909,Human_RBP_ID_11673829,Human_RBP_ID_16988097,Human_RBP_ID_17062302,Human_RBP_ID_17108728,Human_RBP_ID_17184754,Human_RBP_ID_17232830,Human_RBP_ID_17349142,Human_RBP_ID_17465715,Human_RBP_ID_17682407,Human_RBP_ID_17799185,Human_RBP_ID_19583055,Human_RBP_ID_22032844,Human_RBP_ID_22164902,Human_RBP_ID_22381270,Human_RBP_ID_22491601,Human_RBP_ID_22791713,Human_RBP_ID_22893024,Human_RBP_ID_23154680,Human_RBP_ID_23268017,Human_RBP_ID_23514978,Human_RBP_ID_24404236,Human_RBP_ID_24461873,Human_RBP_ID_24897099,Human_RBP_ID_26605381,Human_RBP_ID_26894584,Human_RBP_ID_27204982,Human_RBP_ID_27414345,Human_RBP_ID_27618969 Human_Splice_Rec_1258549,Human_Splice_Rec_1258564 Human_miRNA_ID_2374035,Human_miRNA_ID_2374036,Human_miRNA_ID_2374037,Human_miRNA_ID_3171735 RMVar_hsa_circ_150673,RMVar_hsa_circ_377612,RMVar_hsa_circ_150677,RMVar_hsa_circ_150678,RMVar_hsa_circ_150684,RMVar_hsa_circ_150683,RMVar_hsa_circ_378367,RMVar_hsa_circ_378681,RMVar_hsa_circ_379048,RMVar_hsa_circ_378349,RMVar_hsa_circ_150681,RMVar_hsa_circ_150682,RMVar_hsa_circ_150680 116939 RMVar_ID_116939 Human_SNP_ID_813693521 m1A Human chr11 - 57308473 57308473 57308473 TGAGACAAGTGGGCCAGAGACCCAGGGTGAAGATTACTCCTCGTCTTCCTTGGAGCCACACCCTG TGAGACAAGTGGGCCAGAGACCCAGGGTGAAGTTTACTCCTCGTCTTCCTTGGAGCCACACCCTG T A TNKS1BP1 Ensembl:ENSG00000149115 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:57308422..57308579 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_RBP_ID_866467,Human_RBP_ID_2271780,Human_RBP_ID_27412074 Human_Splice_Rec_1239441,Human_Splice_Rec_1239461 116940 RMVar_ID_116940 Human_SNP_ID_813696314 m1A Human chr11 + 35619747 35619747 35619747 TGTTGCAGTCAGTGTGCGTGTTCCGCGAGCGGACCGCGCGGCGCGTCCTGGAGCTGCACCGCGGA TGTTGCAGTCAGTGTGCGTGTTCCGCGAGCGGGCCGCGCGGCGCGTCCTGGAGCTGCACCGCGGA A G FJX1 Ensembl:ENSG00000179431 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:35619702..35619900 26863196 MeRIP-seq:(Medium) rs202089278 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_395740 116941 RMVar_ID_116941 Human_SNP_ID_813703563 m1A Human chr11 - 2397200 2397200 2397200 GGACGGGCGGGCTGGGTGGACACAGCCCCCCAAGTTGGCCAAGCTGAGTCTCTGGGCGAGTGGCT GGACGGGCGGGCTGGGTGGACACAGCCCCCCAGGTTGGCCAAGCTGAGTCTCTGGGCGAGTGGCT T C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr11:2397176..2397200 26863196 MeRIP-seq:(Medium) rs1049549 Functional Loss SNV ICGC 33..33 33 LUSC 1 - GWAS_ID_6813 116942 RMVar_ID_116942 Human_SNP_ID_813706483 m1A Human chr11 + 12726091 12726090 12726091 GAAACAGGCACAGTCCTGTCTTCAAGGAACATAAAATAGCAGATGACACGGCTGAGCAGGAATGA GAAACAGGCACAGTCCTGTCTTCAAGGAACAT_AAATAGCAGATGACACGGCTGAGCAGGAATGA TA T TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr11:12726089..12726177 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2257327 RMVar_hsa_circ_81333,RMVar_hsa_circ_109654,RMVar_hsa_circ_10471,RMVar_hsa_circ_148280,RMVar_hsa_circ_148281,RMVar_hsa_circ_314206,RMVar_hsa_circ_315627,RMVar_hsa_circ_59598,RMVar_hsa_circ_148282 116943 RMVar_ID_116943 Human_SNP_ID_813714463 m1A Human chr11 - 57808539 57808539 57808539 TTGAGGTAACAGTTAGCATTCAACTCCTCACCAATTAATTCTTTGTTGCGAGCATCCACAGCCAG TTGAGGTAACAGTTAGCATTCAACTCCTCACCGATTAATTCTTTGTTGCGAGCATCCACAGCCAG T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:57808412..57809446 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium clear_cell_carcinoma 30 uterus 116944 RMVar_ID_116944 Human_SNP_ID_813718082 m1A Human chr11 + 73290285 73290280 73290285 AGAGAGAGGGGGAAAGAAAAGAAAGGAAGGAAAGAAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA AGAGAGAGGGGGAAAGAAAAGAAAGGAA_____GAAAGAAAGAAAGAAAGAAAAGAAAGAAAGAA AGGAAA A P2RY6 Ensembl:ENSG00000171631 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:73290238..73290328 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 29..33 33 SKCA 1 - 116945 RMVar_ID_116945 Human_SNP_ID_813729797 m1A Human chr11 - 62677932 62677932 62677932 GAGAGGCGGAGGGAAAAGGCCGAGGAGTTAGCAGCCAGGTCTGGGCAGGGGAAATGATGGATAGC GAGAGGCGGAGGGAAAAGGCCGAGGAGTTAGCGGCCAGGTCTGGGCAGGGGAAATGATGGATAGC T C UBXN1 Ensembl:ENSG00000162191 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:62677926..62678025 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_4167105,Human_RBP_ID_9362358,Human_RBP_ID_17649622,Human_RBP_ID_26318525 Human_Splice_Rec_1248759,Human_Splice_Rec_1248771,Human_Splice_Rec_1248781,Human_Splice_Rec_1248789,Human_Splice_Rec_1248799,Human_Splice_Rec_1248813,Human_Splice_Rec_1248841,Human_Splice_Rec_1248857,Human_Splice_Rec_1248869,Human_Splice_Rec_1248881,Human_Splice_Rec_1248893,Human_Splice_Rec_1248905 RMVar_hsa_circ_86665,RMVar_hsa_circ_88675,RMVar_hsa_circ_83941,RMVar_hsa_circ_150233,RMVar_hsa_circ_150235,RMVar_hsa_circ_150234,RMVar_hsa_circ_62598 116946 RMVar_ID_116946 Human_SNP_ID_813736640 m1A Human chr11 + 66744816 66744816 66744816 GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGGGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66744733..66748441 26863196 MeRIP-seq:(Medium) rs1333256924 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_4184254,Human_RBP_ID_5138685,Human_RBP_ID_18416934 116947 RMVar_ID_116947 Human_SNP_ID_813736647 m1A Human chr11 + 66744816 66744816 66744816 GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGAGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG GGCACTGGCGGAGTTCCAAGCCCGGGCTGAGGCGGGGGCGGCGGCGGCGGCGGCGGCGGCGGGCG A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:66744733..66748441 26863196 MeRIP-seq:(Medium) rs1333256924 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,lung small_cell_carcinoma 8 lung,oesophagus Human_RBP_ID_4184254,Human_RBP_ID_5138685,Human_RBP_ID_18416934 116948 RMVar_ID_116948 Human_SNP_ID_813757296 m1A Human chr11 + 82900327 82900327 82900327 GGTTGGCAAGTGTAGGCTGCCGAGGGCCCTTAAGGCCGGCCGGAGGGCTATGGTGGCCCAGGGCG GGTTGGCAAGTGTAGGCTGCCGAGGGCCCTTACGGCCGGCCGGAGGGCTATGGTGGCCCAGGGCG A C DDIAS Ensembl:ENSG00000165490 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:82900278..82900429 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 upper_arm desmoplastic,skin desmoplastic 2 skin,upper extremity 116949 RMVar_ID_116949 Human_SNP_ID_813767395 m1A Human chr11 + 72781804 72781804 72781804 GGGTCCCGCCGCCCGGCCCCGCCCCGGGCCCCAGCCCCGCGCGCCCCTCCCGGCTAGGCTGGGGG GGGTCCCGCCGCCCGGCCCCGCCCCGGGCCCCTGCCCCGCGCGCCCCTCCCGGCTAGGCTGGGGG A T - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr11:72781106..72781900 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 6 breast 116950 RMVar_ID_116950 Human_SNP_ID_813769429 m1A Human chr11 - 19715450 19715450 19715450 CACCGACTGCCCACTACACCTCATAAACCCCAAGTCCATGGATGAAGGGAAACCCCATGCAGAAG CACCGACTGCCCACTACACCTCATAAACCCCACGTCCATGGATGAAGGGAAACCCCATGCAGAAG T G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr11:19715439..19715550 26863196 MeRIP-seq:(Medium) rs1319701 Functional Loss SNV ICGC 33..33 33 LAML 2 - GWAS_ID_6826,GWAS_ID_6827,GWAS_ID_6828,GWAS_ID_6829,GWAS_ID_6830,GWAS_ID_6831,GWAS_ID_6832 116951 RMVar_ID_116951 Human_SNP_ID_813770114 m1A Human chr11 + 68365690 68365690 68365690 CCACGGGTGTGCAGCTGCAGGACAACGGCAGGACGTGTAAGGCAGGTGAGGCGGTGGGACGGGAC CCACGGGTGTGCAGCTGCAGGACAACGGCAGGCCGTGTAAGGCAGGTGAGGCGGTGGGACGGGAC A C LRP5 Ensembl:ENSG00000162337 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr11:68365640..68365750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_3939594,Human_RBP_ID_5550128,Human_RBP_ID_17805941,Human_RBP_ID_18468985,Human_RBP_ID_27154433 Human_Splice_Rec_1268515,Human_Splice_Rec_1268557 RMVar_hsa_circ_60233,RMVar_hsa_circ_151165,RMVar_hsa_circ_89754,RMVar_hsa_circ_280139,RMVar_hsa_circ_322194,RMVar_hsa_circ_371997,RMVar_hsa_circ_349419,RMVar_hsa_circ_123648,RMVar_hsa_circ_112264,RMVar_hsa_circ_65992,RMVar_hsa_circ_81769,RMVar_hsa_circ_151166,RMVar_hsa_circ_151161,RMVar_hsa_circ_151163,RMVar_hsa_circ_151164,RMVar_hsa_circ_151162,RMVar_hsa_circ_118834,RMVar_hsa_circ_331637,RMVar_hsa_circ_293205,RMVar_hsa_circ_124136,RMVar_hsa_circ_65217,RMVar_hsa_circ_36292,RMVar_hsa_circ_151173,RMVar_hsa_circ_22503,RMVar_hsa_circ_151174,RMVar_hsa_circ_151172,RMVar_hsa_circ_151176,RMVar_hsa_circ_94107,RMVar_hsa_circ_266158,RMVar_hsa_circ_86911,RMVar_hsa_circ_151177,RMVar_hsa_circ_122875,RMVar_hsa_circ_119098,RMVar_hsa_circ_151178,RMVar_hsa_circ_151179,RMVar_hsa_circ_151180 116952 RMVar_ID_116952 Human_SNP_ID_813777161 m1A Human chr11 + 64244944 64244944 64244944 CCCCAGGAAATCTCTTACCTCTGTGGGTTTGTAACAGTCAACCAGCAGCTCCTAGCAGAGGATGG CCCCAGGAAATCTCTTACCTCTGTGGGTTTGTGACAGTCAACCAGCAGCTCCTAGCAGAGGATGG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr11:64244678..64245013;chr11:64244676..64245275 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 3 head and neck 116953 RMVar_ID_116953 Human_SNP_ID_813777190 m1A Human chr11 - 62841702 62841702 62841702 TCCGAGGACAATATATTAAATGGATTTTTGGAAATAGGAGATGGAATAGGAGCTTGCTCCGTCCA TCCGAGGACAATATATTAAATGGATTTTTGGAGATAGGAGATGGAATAGGAGCTTGCTCCGTCCA T C WDR74,RNU2-2P Ensembl:ENSG00000133316,Ensembl:ENSG00000222328 Protein coding,snRNA 5'UTR,exon GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:62841651..62841798;chr11:62841651..62841725 26863196 MeRIP-seq:(Medium) rs75829596 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_29144,Human_RBP_ID_108214,Human_RBP_ID_226083,Human_RBP_ID_292750,Human_RBP_ID_399282,Human_RBP_ID_748658,Human_RBP_ID_807408,Human_RBP_ID_867596,Human_RBP_ID_1162482,Human_RBP_ID_1354650,Human_RBP_ID_1458346,Human_RBP_ID_1780689,Human_RBP_ID_2273423,Human_RBP_ID_3377231,Human_RBP_ID_4167779,Human_RBP_ID_5087214,Human_RBP_ID_5093729,Human_RBP_ID_5170152,Human_RBP_ID_5246222,Human_RBP_ID_5282091,Human_RBP_ID_5416110,Human_RBP_ID_5436637,Human_RBP_ID_5460528,Human_RBP_ID_5489913,Human_RBP_ID_5549530,Human_RBP_ID_6083006,Human_RBP_ID_8246443,Human_RBP_ID_8354163,Human_RBP_ID_8770659,Human_RBP_ID_9004662,Human_RBP_ID_9321480,Human_RBP_ID_9344015,Human_RBP_ID_9415789,Human_RBP_ID_9643476,Human_RBP_ID_11660350,Human_RBP_ID_17074734,Human_RBP_ID_17235481,Human_RBP_ID_17348931,Human_RBP_ID_17467294,Human_RBP_ID_17560835,Human_RBP_ID_17581609,Human_RBP_ID_17599310,Human_RBP_ID_17668897,Human_RBP_ID_17673035,Human_RBP_ID_17682292,Human_RBP_ID_17798358,Human_RBP_ID_18174124,Human_RBP_ID_18198708,Human_RBP_ID_18205804,Human_RBP_ID_18251321,Human_RBP_ID_18409261,Human_RBP_ID_18432907,Human_RBP_ID_18478901,Human_RBP_ID_18544190,Human_RBP_ID_18609876,Human_RBP_ID_18926311,Human_RBP_ID_18934155,Human_RBP_ID_19051873,Human_RBP_ID_19582360,Human_RBP_ID_21959554,Human_RBP_ID_22032276,Human_RBP_ID_22163685,Human_RBP_ID_22353723,Human_RBP_ID_22369769,Human_RBP_ID_22380845,Human_RBP_ID_22522219,Human_RBP_ID_22537503,Human_RBP_ID_22569316,Human_RBP_ID_22641357,Human_RBP_ID_22736050,Human_RBP_ID_22791008,Human_RBP_ID_22891686,Human_RBP_ID_23110222,Human_RBP_ID_23113253,Human_RBP_ID_23124548,Human_RBP_ID_23154306,Human_RBP_ID_23267866,Human_RBP_ID_23305104,Human_RBP_ID_23511348,Human_RBP_ID_24403413,Human_RBP_ID_24463012,Human_RBP_ID_24543034,Human_RBP_ID_24551148,Human_RBP_ID_24557602,Human_RBP_ID_24893233,Human_RBP_ID_26405002,Human_RBP_ID_26575677,Human_RBP_ID_26605144,Human_RBP_ID_26747652,Human_RBP_ID_26776752,Human_RBP_ID_26893087,Human_RBP_ID_27154188,Human_RBP_ID_27203647,Human_RBP_ID_27413258,Human_RBP_ID_27556980,Human_RBP_ID_27618655,Human_RBP_ID_27796769 RMVar_hsa_circ_150292,RMVar_hsa_circ_122119,RMVar_hsa_circ_122923,RMVar_hsa_circ_118375,RMVar_hsa_circ_150294,RMVar_hsa_circ_150295,RMVar_hsa_circ_100272,RMVar_hsa_circ_150297,RMVar_hsa_circ_81163,RMVar_hsa_circ_150300,RMVar_hsa_circ_109781,RMVar_hsa_circ_150301 116954 RMVar_ID_116954 Human_SNP_ID_813788090 m1A Human chr11 + 62572685 62572685 62572685 TGCGGAGAGCACGCGGACCTGAGCCCCGCTGTACTGAGCAGCGATGAGAGCCTTGAAGGCCCTCC TGCGGAGAGCACGCGGACCTGAGCCCCGCTGTTCTGAGCAGCGATGAGAGCCTTGAAGGCCCTCC A T - - Other Unknown GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580 HEK293T,Starvation treatment chr11:62572626..62572738 26863410 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 1 uterus 116955 RMVar_ID_116955 Human_SNP_ID_813792574 m1A Human chr11 - 66744764 66744764 66744764 CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCACGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG CTCCGCCAGTGCCCACGCCCGAGTCCACGCCCTCGCCCGGCAGCGCGAGCCCATCCCTTCCCGCG T A - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:66744718..66744847 26863196 MeRIP-seq:(Medium) rs903238296 Functional Loss SNV ICGC 33..33 33 HNSC 1 - 116956 RMVar_ID_116956 Human_SNP_ID_813795137 m1A Human chr11 + 66707562 66707562 66707562 TCCAGTCCATGAGGTAGAGCAGGTCCTGGAACACCTTCTGCAGCTCCAGGTTGAGGAGGAGCCGC TCCAGTCCATGAGGTAGAGCAGGTCCTGGAACGCCTTCTGCAGCTCCAGGTTGAGGAGGAGCCGC A G - - Other Unknown GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr11:66707438..66707650 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 5 stomach RMVar_hsa_circ_150940 116957 RMVar_ID_116957 Human_SNP_ID_813802136 m1A Human chr11 - 607903 607903 607903 TCCGCAGCTGCTTCGTCTTCTTGATGGAGAAGAGGGGTGAGGGGTTCTCCTTCCTCTGCTCCTTA TCCGCAGCTGCTTCGTCTTCTTGATGGAGAAGTGGGGTGAGGGGTTCTCCTTCCTCTGCTCCTTA T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:607568..607967 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116958 RMVar_ID_116958 Human_SNP_ID_813805940 m1A Human chr11 - 65897005 65897005 65897005 CATCTGTGGCCTTCCATTTCTTATTCCTTAGAAGTTCCACCTGGTGCCAAGCATCAACACCATGA CATCTGTGGCCTTCCATTTCTTATTCCTTAGAGGTTCCACCTGGTGCCAAGCATCAACACCATGA T C FOSL1 Ensembl:ENSG00000175592 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65896984..65897059 26863196 MeRIP-seq:(Medium) rs757312993 Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 4 ovary Human_RBP_ID_32642 Human_Splice_Rec_1261102,Human_Splice_Rec_1261110,Human_Splice_Rec_1261114 RMVar_hsa_circ_290135,RMVar_hsa_circ_336721 116959 RMVar_ID_116959 Human_SNP_ID_813808470 m1A Human chr11 + 126271396 126271396 126271396 GTGCCCATCCTCCAACCCCCCAACCATGTGGGAAGGAAATGTTTGGCCCTCTGACCCTAACTACA GTGCCCATCCTCCAACCCCCCAACCATGTGGGGAGGAAATGTTTGGCCCTCTGACCCTAACTACA A G FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:126271392..126271490 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_1776738,Human_RBP_ID_22572004 116960 RMVar_ID_116960 Human_SNP_ID_813822786 m1A Human chr11 + 67442477 67442477 67442477 CCAGAAAGGCACCCCCTCCACTGGCCTCCACAATCACCGCCAGGAACTTGGGGTTGACGGCGCAG CCAGAAAGGCACCCCCTCCACTGGCCTCCACACTCACCGCCAGGAACTTGGGGTTGACGGCGCAG A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr11:67442426..67442575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 116961 RMVar_ID_116961 Human_SNP_ID_813829911 m1A Human chr11 + 27363041 27363041 27363041 GGAATTGCTGCAGCTCAGCGGCAGCGGCGGCGACGGCGAGCGCACCACCTCCAGCCCCTGCCCAC GGAATTGCTGCAGCTCAGCGGCAGCGGCGGCGGCGGCGAGCGCACCACCTCCAGCCCCTGCCCAC A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr11:27362973..27363142 26863196 MeRIP-seq:(Medium) rs375252730 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 116962 RMVar_ID_116962 Human_SNP_ID_813836300 m1A Human chr11 - 6569598 6569598 6569598 CTCCTCTGATCCATTCTCCATGTTGCATCCAGAGTGATCCTTCCAACACACAAAAAGGATATTGT CTCCTCTGATCCATTCTCCATGTTGCATCCAGTGTGATCCTTCCAACACACAAAAAGGATATTGT T A lnc-RRP8-5 RNACentral:URS00008C19E7 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:6569590..6569817 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116963 RMVar_ID_116963 Human_SNP_ID_813866056 m1A Human chr11 + 68019765 68019765 68019765 CTGGGCGGGCCCCAGGAGACGGGGCAGCTGCTAGAGCACAGGTTCGACTACATCTTCTTCACAGG CTGGGCGGGCCCCAGGAGACGGGGCAGCTGCTTGAGCACAGGTTCGACTACATCTTCTTCACAGG A T ALDH3B1 Ensembl:ENSG00000006534 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:68019670..68019867 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 7 kidney Human_Splice_Rec_1267730,Human_Splice_Rec_1267731,Human_Splice_Rec_1267748,Human_Splice_Rec_1267749,Human_Splice_Rec_1267760,Human_Splice_Rec_1267761,Human_Splice_Rec_1267776,Human_Splice_Rec_1267777,Human_Splice_Rec_1267808,Human_Splice_Rec_1267809,Human_Splice_Rec_1267826,Human_Splice_Rec_1267827,Human_Splice_Rec_1267848,Human_Splice_Rec_1267849 116964 RMVar_ID_116964 Human_SNP_ID_813866431 m1A Human chr11 - 72003482 72003482 72003482 AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGACCTCACCTGGTCCTCCGCCTACTGTCCCTCTC AGTGAGTGGCCCCACCTGTGTCCCCGATGCTGCCCTCACCTGGTCCTCCGCCTACTGTCCCTCTC T G NUMA1 Ensembl:ENSG00000137497 Protein coding exon GSE97419:GSM2564283,GSM2564284,GSM2564285,GSM2564286 HEK293T cells, from four datasets - 29072297 m1A-MAP:(High) rs949323 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue Human_RBP_ID_871459,Human_RBP_ID_9276008,Human_RBP_ID_17649229,Human_RBP_ID_26406744 Human_Splice_Rec_1272206,Human_Splice_Rec_1272230,Human_Splice_Rec_1272278,Human_Splice_Rec_1272330,Human_Splice_Rec_1272382,Human_Splice_Rec_1272428,Human_Splice_Rec_1272476,Human_Splice_Rec_1272522 Human_miRNA_ID_188716,Human_miRNA_ID_2007100 Clinvar_Rec_361,Clinvar_Rec_362,Clinvar_Rec_3376,Clinvar_Rec_3377 GWAS_ID_9354,GWAS_ID_9355,GWAS_ID_9356,GWAS_ID_9357,GWAS_ID_9358,GWAS_ID_9359,GWAS_ID_9360,GWAS_ID_9361,GWAS_ID_9362,GWAS_ID_9363 RMVar_hsa_circ_94569,RMVar_hsa_circ_103869,RMVar_hsa_circ_151493,RMVar_hsa_circ_151494 116965 RMVar_ID_116965 Human_SNP_ID_813867828 m1A Human chr11 + 755885 755876 755885 TTGGCTTTTGAAAACTATTTCCCTAGCCATCGACGAGTACAAGCCCCAGGATGCTACCACCAACC TTGGCTTTTGAAAACTATTTCCCT_________CGAGTACAAGCCCCAGGATGCTACCACCAACC TAGCCATCGA T TALDO1 Ensembl:ENSG00000177156 Protein coding 3'UTR GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782894,GSM1782895;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA rearranged at 60c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA heat shock 4h chr11:755876..755900;chr11:755876..755950;chr11:755876..755925 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 25..33 33 STAD 1 - Human_RBP_ID_227182,Human_RBP_ID_871760,Human_RBP_ID_4178978,Human_RBP_ID_22434127,Human_RBP_ID_26803069 Human_Splice_Rec_1194974,Human_Splice_Rec_1194982,Human_Splice_Rec_1194984,Human_Splice_Rec_1194996,Human_Splice_Rec_1195006,Human_Splice_Rec_1195012 Human_miRNA_ID_2040080,Human_miRNA_ID_3019062 RMVar_hsa_circ_8060,RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_373496,RMVar_hsa_circ_147449,RMVar_hsa_circ_291586,RMVar_hsa_circ_147451,RMVar_hsa_circ_147452 116966 RMVar_ID_116966 Human_SNP_ID_813867868 m1A Human chr11 - 119048494 119048494 119048494 GAACGGGAAAAAGCTGCCAACAGCTTGGAAGCATTCATATTTGAGACCCAGGTCAGTGGGCAGGA GAACGGGAAAAAGCTGCCAACAGCTTGGAAGCGTTCATATTTGAGACCCAGGTCAGTGGGCAGGA T C HYOU1 Ensembl:ENSG00000149428 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs568922 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_390234 Human_Splice_Rec_1306266,Human_Splice_Rec_1306267,Human_Splice_Rec_1306360,Human_Splice_Rec_1306361,Human_Splice_Rec_1306410,Human_Splice_Rec_1306411,Human_Splice_Rec_1306496,Human_Splice_Rec_1306497,Human_Splice_Rec_1306514,Human_Splice_Rec_1306548,Human_Splice_Rec_1306549 Human_miRNA_ID_473471,Human_miRNA_ID_1099548 GWAS_ID_11571,GWAS_ID_11572,GWAS_ID_11573,GWAS_ID_11574,GWAS_ID_11575,GWAS_ID_11576,GWAS_ID_11577,GWAS_ID_11578 RMVar_hsa_circ_62478,RMVar_hsa_circ_20276,RMVar_hsa_circ_78758,RMVar_hsa_circ_153460 116967 RMVar_ID_116967 Human_SNP_ID_813869804 m1A Human chr11 + 67291662 67291662 67291662 GCGATGTGTACCGCGTGTGGAAGCGGGGTGAGAGCCTGCGAGTAGACACCAGTCTCCTGGGCTTC GCGATGTGTACCGCGTGTGGAAGCGGGGTGAGCGCCTGCGAGTAGACACCAGTCTCCTGGGCTTC A C ANKRD13D Ensembl:ENSG00000172932 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:67291612..67291692 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_401938,Human_RBP_ID_866749,Human_RBP_ID_3939549,Human_RBP_ID_9362624,Human_RBP_ID_18972370,Human_RBP_ID_27836426 Human_Splice_Rec_1265560,Human_Splice_Rec_1265568,Human_Splice_Rec_1265569,Human_Splice_Rec_1265600,Human_Splice_Rec_1265601,Human_Splice_Rec_1265624,Human_Splice_Rec_1265625,Human_Splice_Rec_1265648,Human_Splice_Rec_1265649,Human_Splice_Rec_1265654,Human_Splice_Rec_1265655,Human_Splice_Rec_1265665 Human_miRNA_ID_3114563 RMVar_hsa_circ_151040,RMVar_hsa_circ_82821,RMVar_hsa_circ_315908 116968 RMVar_ID_116968 Human_SNP_ID_813870278 m1A Human chr11 + 69648038 69648038 69648038 TTTCCAATCCGCCCTCCATGGTGGCAGCGGGGAGCGTGGTGGCCGCAGTGCAAGGCCTGAACCTG TTTCCAATCCGCCCTCCATGGTGGCAGCGGGGTGCGTGGTGGCCGCAGTGCAAGGCCTGAACCTG A T CCND1 Ensembl:ENSG00000110092 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:69648001..69648100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_29878,Human_RBP_ID_402555,Human_RBP_ID_22433836 Human_Splice_Rec_1269982,Human_Splice_Rec_1269990,Human_Splice_Rec_1269994 RMVar_hsa_circ_151347,RMVar_hsa_circ_12261,RMVar_hsa_circ_86573 116969 RMVar_ID_116969 Human_SNP_ID_813873088 m1A Human chr11 - 67428556 67428556 67428556 TGCCTTCCTCCGTCTCCAAATCCAAATCAAACACGGCCGCCATGGCGGCGCCGGCCCCGCGGGCC TGCCTTCCTCCGTCTCCAAATCCAAATCAAACGCGGCCGCCATGGCGGCGCCGGCCCCGCGGGCC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution chr11:67428476..67428651;chr11:67428501..67428659 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 116970 RMVar_ID_116970 Human_SNP_ID_813881795 m1A Human chr11 + 65211360 65211360 65211360 CGTCTGCCAAGCCTCGCCTCCTACCACACCACACCAGGCCACCCCAGCTGCAAGTGCCTTCCTTG CGTCTGCCAAGCCTCGCCTCCTACCACACCACCCCAGGCCACCCCAGCTGCAAGTGCCTTCCTTG A C CAPN1 Ensembl:ENSG00000014216 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr11:65211310..65211648 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_5110863,Human_RBP_ID_17649704 Human_miRNA_ID_2684724,Human_miRNA_ID_2759267 RMVar_hsa_circ_106747,RMVar_hsa_circ_150600 116971 RMVar_ID_116971 Human_SNP_ID_813890763 m1A Human chr11 - 3824044 3824044 3824044 TTGAGGCCGAAGTTGAGGCGGCAGAGCGGGCGATAGCAGGAACACGGGGAGGTGCAGCTGAGGTA TTGAGGCCGAAGTTGAGGCGGCAGAGCGGGCGGTAGCAGGAACACGGGGAGGTGCAGCTGAGGTA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution chr11:3823726..3824375;chr11:3823676..3824350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 52 pancreas 116972 RMVar_ID_116972 Human_SNP_ID_813896030 m1A Human chr11 + 67489362 67489362 67489362 CTGGAGGGCCAGCGGCACTGCTGCGGTGTTGCACAGATGCGTGAACACAGCTCCCTGGGCCATGC CTGGAGGGCCAGCGGCACTGCTGCGGTGTTGCGCAGATGCGTGAACACAGCTCCCTGGGCCATGC A G AIP Ensembl:ENSG00000110711 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr11:67489251..67489475 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_Splice_Rec_1266742,Human_Splice_Rec_1266743,Human_Splice_Rec_1266760,Human_Splice_Rec_1266761 RMVar_hsa_circ_103564,RMVar_hsa_circ_114401,RMVar_hsa_circ_151067,RMVar_hsa_circ_151068 116973 RMVar_ID_116973 Human_SNP_ID_813924638 m1A Human chr11 - 47182428 47182428 47182428 GCTTATGCCCAGCAGTTGGCTGACTGGGCCCGAAAGTGGAGGGGGACCGTGGAGAAGGGTGAGCC GCTTATGCCCAGCAGTTGGCTGACTGGGCCCGGAAGTGGAGGGGGACCGTGGAGAAGGGTGAGCC T C PACSIN3 Ensembl:ENSG00000165912 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr11:47180591..47182452 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_9362180,Human_RBP_ID_18973545,Human_RBP_ID_23507040 Human_Splice_Rec_1235445,Human_Splice_Rec_1235463,Human_Splice_Rec_1235481,Human_Splice_Rec_1235503,Human_Splice_Rec_1235519,Human_Splice_Rec_1235531,Human_Splice_Rec_1235543,Human_Splice_Rec_1235551 RMVar_hsa_circ_80682,RMVar_hsa_circ_149492,RMVar_hsa_circ_76795,RMVar_hsa_circ_149491 116974 RMVar_ID_116974 Human_SNP_ID_877075152 m1A Human chr9 + 21971204 21971201 21971205 GCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGC GCAGCTCCGCCACTCGGGCGCTGCCCATCA____GACCTGCCAGAGAGAACAGAATGGTCAGAGC ATCAT A AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21970862..21971254 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 31..34 33 ESCA 1 - 116975 RMVar_ID_116975 Human_SNP_ID_877075152 m1A Human chr9 - 21971205 21971201 21971205 GGCTCTGACCATTCTGTTCTCTCTGGCAGGTCATGATGATGGGCAGCGCCCGAGTGGCGGAGCTG GGCTCTGACCATTCTGTTCTCTCTGGCAGGTC____TGATGGGCAGCGCCCGAGTGGCGGAGCTG ATCAT A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21970863..21971278 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..36 33 ESCA 1 - Human_RBP_ID_5024659,Human_RBP_ID_9235428,Human_RBP_ID_18134013,Human_RBP_ID_24523183 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1275357 116976 RMVar_ID_116976 Human_SNP_ID_877076448 m1A Human chr9 + 129829230 129829230 129829230 CACTCACGCTCAGGCTCTGGCTTCTCCGTGTCACCTACTCTCAAGGGCCGGGCCTTGGGCTCTTC CACTCACGCTCAGGCTCTGGCTTCTCCGTGTCGCCTACTCTCAAGGGCCGGGCCTTGGGCTCTTC A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:129829199..129829313 26863196 MeRIP-seq:(Medium) rs3818553 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,ESCA 2 stomach Clinvar_Rec_690,Clinvar_Rec_7102 GWAS_ID_14739,GWAS_ID_14740,GWAS_ID_14741,GWAS_ID_14742,GWAS_ID_14743,GWAS_ID_14744,GWAS_ID_14745,GWAS_ID_14746,GWAS_ID_14747,GWAS_ID_14748,GWAS_ID_14749,GWAS_ID_14750,GWAS_ID_14751,GWAS_ID_14752,GWAS_ID_14753,GWAS_ID_14754,GWAS_ID_14755,GWAS_ID_14756,GWAS_ID_14757,GWAS_ID_14758,GWAS_ID_14759,GWAS_ID_14760,GWAS_ID_14761,GWAS_ID_14762,GWAS_ID_14763,GWAS_ID_14764,GWAS_ID_14765,GWAS_ID_14766,GWAS_ID_14767,GWAS_ID_14768,GWAS_ID_14769,GWAS_ID_14770,GWAS_ID_14771,GWAS_ID_14772,GWAS_ID_14773,GWAS_ID_14774,GWAS_ID_14775,GWAS_ID_14776,GWAS_ID_14777,GWAS_ID_14778,GWAS_ID_14779,GWAS_ID_14780,GWAS_ID_14781,GWAS_ID_14782,GWAS_ID_14783,GWAS_ID_14784,GWAS_ID_14785,GWAS_ID_14786,GWAS_ID_14787,GWAS_ID_14788,GWAS_ID_14789,GWAS_ID_14790,GWAS_ID_14791,GWAS_ID_14792,GWAS_ID_14793,GWAS_ID_14794,GWAS_ID_14795,GWAS_ID_14796,GWAS_ID_14797,GWAS_ID_14798,GWAS_ID_14799,GWAS_ID_14800 116977 RMVar_ID_116977 Human_SNP_ID_877077293 m1A Human chr9 - 125143058 125143058 125143058 GGGGTCGCCGGGCCCGGAGAGGCGGGGCGTGGAGGGGGCAGTGCACGGTCGGGAACGGGTGGGCA GGGGTCGCCGGGCCCGGAGAGGCGGGGCGTGGGGGGGGCAGTGCACGGTCGGGAACGGGTGGGCA T C SCAI Ensembl:ENSG00000173611 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125143051..125143267 26863196 MeRIP-seq:(Medium) rs976234954 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_92131,RMVar_hsa_circ_259541,RMVar_hsa_circ_96546,RMVar_hsa_circ_259549 116978 RMVar_ID_116978 Human_SNP_ID_877084765 m1A Human chr9 - 136414627 136414627 136414627 TGGGATCCACACCTGTTAGCCGGGGCTGCAGAACCACATCAGCCAGTAAGGCAACCACCGTGTCC TGGGATCCACACCTGTTAGCCGGGGCTGCAGAGCCACATCAGCCAGTAAGGCAACCACCGTGTCC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:136414576..136416096 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine 116979 RMVar_ID_116979 Human_SNP_ID_877106537 m1A Human chr9 + 137426328 137426310 137426329 TTCCAGCGAGGAGTGGCCAACTTCCAGCTGGCAAGGTGAGTACAGGGGTGCCTTGTTCCTTCTCT TTCCAGCGAGGAGTG___________________GGTGAGTACAGGGGTGCCTTGTTCCTTCTCT GGCCAACTTCCAGCTGGCAA G NOXA1 Ensembl:ENSG00000188747 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137426285..137429381 32194978 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 16..34 33 LUSC 1 - Human_Splice_Rec_1103808,Human_Splice_Rec_1103809,Human_Splice_Rec_1103834,Human_Splice_Rec_1103835 RMVar_hsa_circ_361152 116980 RMVar_ID_116980 Human_SNP_ID_877122226 m1A Human chr9 - 98119152 98119151 98119152 CGGGCGCGGCGACCGGGAGCCGGACCCCTGGGAGGTCGGAGCTTGTCGAGGGATGCGGCTGGCGC CGGGCGCGGCGACCGGGAGCCGGACCCCTGGG_GGTCGGAGCTTGTCGAGGGATGCGGCTGGCGC CT C TRIM14 Ensembl:ENSG00000106785 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:98119104..98119265 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..33 33 LUSC 1 - Human_RBP_ID_256529,Human_RBP_ID_798581,Human_RBP_ID_5154962,Human_RBP_ID_23094616,Human_RBP_ID_26360906 RMVar_hsa_circ_54087 116981 RMVar_ID_116981 Human_SNP_ID_877122863 m1A Human chr9 + 120580030 120580030 120580030 GCGTTGGTGTCTGTGGCGGCGGCGCCACTAGTACCCCCCGCGATAGCGACCCGCCGGGCTCCCCA GCGTTGGTGTCTGTGGCGGCGGCGCCACTAGTCCCCCCCGCGATAGCGACCCGCCGGGCTCCCCA A C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:120579983..120580102 26863196 MeRIP-seq:(Medium) rs1036373453 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,stomach diffuse_adenocarcinoma 4 stomach 116982 RMVar_ID_116982 Human_SNP_ID_877135033 m1A Human chr9 - 132878409 132878409 132878409 CTTGCCCGAGCCGCAGAGCGCGTCAGCCGGGGAGGTCGGGGCGGGGGCGACCCGCGCGACCGAGG CTTGCCCGAGCCGCAGAGCGCGTCAGCCGGGGTGGTCGGGGCGGGGGCGACCCGCGCGACCGAGG T A AK8 Ensembl:ENSG00000165695 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:132878364..132878479;chr9:132878358..132878483 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 116983 RMVar_ID_116983 Human_SNP_ID_877149648 m1A Human chr9 + 133360006 133360003 133360006 TGGAGTACGTGCCTGCCTGCCTGGTGCACCGGAGGAGGAGGAGGGAGGACCAGATGGACGGTGAC TGGAGTACGTGCCTGCCTGCCTGGTGCACC___GGAGGAGGAGGGAGGACCAGATGGACGGTGAC CGGA C SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133359951..133361073 26863196 MeRIP-seq:(Medium) rs781867176 Functional Loss DEL ICGC 31..33 33 PAAD 1 - Human_RBP_ID_714295,Human_RBP_ID_21907286 Human_Splice_Rec_1095618,Human_Splice_Rec_1095628,Human_Splice_Rec_1095632 116984 RMVar_ID_116984 Human_SNP_ID_877159680 m1A Human chr9 + 25677590 25677590 25677590 GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGAGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG GGCACCGTAGTCCAAGGTATCCGCGGGCAGGGCGCGGGCCAGGGCGTGCGCGAGGTCGGGGGTAG A C - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:25677469..25677750 26863196 MeRIP-seq:(Medium) rs10812300 Functional Loss SNV ICGC 33..33 33 LAML 1 - 116985 RMVar_ID_116985 Human_SNP_ID_877173802 m1A Human chr9 - 135501125 135501125 135501125 TTCCCACCCAACTCGGCTGGGCGCCCAGTGTTACCGGTGCTGTCCTCCGACTCGCGGATCATAAG TTCCCACCCAACTCGGCTGGGCGCCCAGTGTTTCCGGTGCTGTCCTCCGACTCGCGGATCATAAG T A C9orf116 Ensembl:ENSG00000160345 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135501026..135501188 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_5018528,Human_RBP_ID_18905752 116986 RMVar_ID_116986 Human_SNP_ID_877176876 m1A Human chr9 - 33941761 33941761 33941761 TACCTCCTGCAGTCTGACAAGCTCATCACTGAATTCTGCTAGTCCAGTAGCAATGTCTTCCTCTT TACCTCCTGCAGTCTGACAAGCTCATCACTGAGTTCTGCTAGTCCAGTAGCAATGTCTTCCTCTT T C UBAP2 Ensembl:ENSG00000137073 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs307658 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,stomach adenocarcinoma,pancreas ductal_carcinoma,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 14 pancreas,stomach,large intestine,breast Human_RBP_ID_961331,Human_RBP_ID_9406861,Human_RBP_ID_17322839,Human_RBP_ID_18908164,Human_RBP_ID_21720118,Human_RBP_ID_27832326 Human_miRNA_ID_2541771,Human_miRNA_ID_2543647,Human_miRNA_ID_2547352,Human_miRNA_ID_2549216,Human_miRNA_ID_2551085,Human_miRNA_ID_2556490,Human_miRNA_ID_2558372,Human_miRNA_ID_2588791 GWAS_ID_7853,GWAS_ID_7854,GWAS_ID_7855,GWAS_ID_7856,GWAS_ID_7857,GWAS_ID_7858,GWAS_ID_7859,GWAS_ID_7860,GWAS_ID_7861,GWAS_ID_7862,GWAS_ID_7863 RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_256405,RMVar_hsa_circ_97502,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_89057,RMVar_hsa_circ_15047,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_111717,RMVar_hsa_circ_256413,RMVar_hsa_circ_256414,RMVar_hsa_circ_377085,RMVar_hsa_circ_256415,RMVar_hsa_circ_377386,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_119979,RMVar_hsa_circ_256418,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_256422,RMVar_hsa_circ_116561,RMVar_hsa_circ_351025,RMVar_hsa_circ_352118,RMVar_hsa_circ_369653,RMVar_hsa_circ_278531,RMVar_hsa_circ_87127,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256433,RMVar_hsa_circ_301404,RMVar_hsa_circ_256425,RMVar_hsa_circ_256427,RMVar_hsa_circ_256428,RMVar_hsa_circ_256429,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_322683,RMVar_hsa_circ_374778,RMVar_hsa_circ_316868,RMVar_hsa_circ_53464,RMVar_hsa_circ_288073,RMVar_hsa_circ_289056,RMVar_hsa_circ_272780,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_256434,RMVar_hsa_circ_256431,RMVar_hsa_circ_256432,RMVar_hsa_circ_256430 116987 RMVar_ID_116987 Human_SNP_ID_877182152 m1A Human chr9 - 127531773 127531773 127531773 AAGCTCCTGCTTGTCCTTCTCTTCCAGAAAAAACCGGGAAGATCCTGACGGAGTTCCTCCAGTTC AAGCTCCTGCTTGTCCTTCTCTTCCAGAAAAACCCGGGAAGATCCTGACGGAGTTCCTCCAGTTC T G NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127531608..127531828;chr9:127531701..127531800;chr9:127531701..127531842 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_5010133 Human_Splice_Rec_1082266,Human_Splice_Rec_1082294,Human_Splice_Rec_1082296,Human_Splice_Rec_1082322 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_122936,RMVar_hsa_circ_259769,RMVar_hsa_circ_346970,RMVar_hsa_circ_259772,RMVar_hsa_circ_357415,RMVar_hsa_circ_43685,RMVar_hsa_circ_343610,RMVar_hsa_circ_90935,RMVar_hsa_circ_259774,RMVar_hsa_circ_275532,RMVar_hsa_circ_259776,RMVar_hsa_circ_259778 116988 RMVar_ID_116988 Human_SNP_ID_877208377 m1A Human chr9 - 130958685 130958685 130958685 GTGATGGCGGTGGTGGTGGTGATGGTGATGACAGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT GTGATGGCGGTGGTGGTGGTGATGGTGATGACGGTGGTGGTGATGGTGGTGATGGTGGTGGTGGT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:130958624..130958723 26863196 MeRIP-seq:(Medium) rs1025790514 Functional Loss SNV ICGC 33..33 33 COCA 1 - 116989 RMVar_ID_116989 Human_SNP_ID_877223868 m1A Human chr9 + 100142648 100142648 100142648 ACAAAGAGTGAATATAGCTGAAGGAGCCAGGGAGCAGAGAGTATATGCATCAGGTATGAGGAAGA ACAAAGAGTGAATATAGCTGAAGGAGCCAGGGTGCAGAGAGTATATGCATCAGGTATGAGGAAGA A T INVS Ensembl:ENSG00000119509 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:100142394..100142834 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_50475,RMVar_hsa_circ_333575,RMVar_hsa_circ_366034,RMVar_hsa_circ_31388,RMVar_hsa_circ_37468,RMVar_hsa_circ_18273,RMVar_hsa_circ_60561 116990 RMVar_ID_116990 Human_SNP_ID_877248877 m1A Human chr9 + 137517307 137517307 137517307 ACTCACTCACTCCACTCTGTCCACTCCATCCCACACTCACTCACTCCACTCTGTCCACTCCATCC ACTCACTCACTCCACTCTGTCCACTCCATCCCTCACTCACTCACTCCACTCTGTCCACTCCATCC A T - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137517264..137517348 26863196 MeRIP-seq:(Medium) rs1370605853 Functional Loss SNV COSMIC 33..33 33 meninges atypical 2 brain 116991 RMVar_ID_116991 Human_SNP_ID_877269120 m1A Human chr9 + 35061688 35061688 35061688 GGAATTCCAATATCTACCTCCCTGTCAAAGCGACCTGTGGGACAGTACACAAACATAAACAGGGC GGAATTCCAATATCTACCTCCCTGTCAAAGCGCCCTGTGGGACAGTACACAAACATAAACAGGGC A C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35061667..35062080 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 116992 RMVar_ID_116992 Human_SNP_ID_877269125 m1A Human chr9 + 35061688 35061688 35061688 GGAATTCCAATATCTACCTCCCTGTCAAAGCGACCTGTGGGACAGTACACAAACATAAACAGGGC GGAATTCCAATATCTACCTCCCTGTCAAAGCGGCCTGTGGGACAGTACACAAACATAAACAGGGC A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35061667..35062080 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 116993 RMVar_ID_116993 Human_SNP_ID_877274893 m1A Human chr9 - 21974809 21974809 21974809 CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCC CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGGTGCAGCATGGAGCCTTCGGCTGACTGGCTGGCC T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:21974720..21974890 26863410 MeRIP-seq:(Medium) rs1554656670 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 7 haematopoietic and lymphoid tissue Human_RBP_ID_92522,Human_RBP_ID_5024668 Clinvar_Rec_190 116994 RMVar_ID_116994 Human_SNP_ID_877278287 m1A Human chr9 + 96854186 96854186 96854186 GTTGTCGCCCGCGTTACAAATGCGCTTTCCCCACCCCCGCCGCCGCTCGCGCCGGGCTCCGGTCC GTTGTCGCCCGCGTTACAAATGCGCTTTCCCCCCCCCCGCCGCCGCTCGCGCCGGGCTCCGGTCC A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:96854142..96854476 26863196 MeRIP-seq:(Medium) rs905099845 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 116995 RMVar_ID_116995 Human_SNP_ID_877279846 m1A Human chr9 + 15479544 15479544 15479544 TATTTGAGGCAGCAACACTTTAAATGGACTGGAATATTAATCACAAGCCAAACAGATATTTAAAC TATTTGAGGCAGCAACACTTTAAATGGACTGGCATATTAATCACAAGCCAAACAGATATTTAAAC A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:15479540..15479675 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 116996 RMVar_ID_116996 Human_SNP_ID_877282483 m1A Human chr9 - 96820556 96820556 96820556 GACAGAGCAAGACTCTATCTCAAAAAAAAGAAAAAAAAAAAAAAAAGATTCACTATTGAACAACC GACAGAGCAAGACTCTATCTCAAAAAAAAGAAGAAAAAAAAAAAAAGATTCACTATTGAACAACC T C ZNF782 Ensembl:ENSG00000196597 Protein coding intron GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:96820542..96820627 26863410 MeRIP-seq:(Medium) rs10979164 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_26238811 RMVar_hsa_circ_258069,RMVar_hsa_circ_258067,RMVar_hsa_circ_258070,RMVar_hsa_circ_258072,RMVar_hsa_circ_258073,RMVar_hsa_circ_258071 116997 RMVar_ID_116997 Human_SNP_ID_877289049 m1A Human chr9 - 134801956 134801956 134801956 GGGGGGCCTGGAGGGCCGGTCTTGCCTTGGAAACCCTGTGAAGAGAGAGTCACTGCACTGACGGT GGGGGGCCTGGAGGGCCGGTCTTGCCTTGGAACCCCTGTGAAGAGAGAGTCACTGCACTGACGGT T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:134801951..134802000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 116998 RMVar_ID_116998 Human_SNP_ID_877303844 m1A Human chr9 - 98996982 98996982 98996982 TTCACCAGAAAGTTCCATGTCTTCAAAGGGGGAGGATGGAGTTGGAGGTGTGTTTATGGGTTCAA TTCACCAGAAAGTTCCATGTCTTCAAAGGGGGCGGATGGAGTTGGAGGTGTGTTTATGGGTTCAA T G - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:98996841..98997075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 116999 RMVar_ID_116999 Human_SNP_ID_877320085 m1A Human chr9 + 21974781 21974777 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTG____GCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC GGCCA G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs587782206 Functional Loss DEL TCGA,ICGC 30..33 33 ESCA,THYM 3 - Clinvar_Rec_186 117000 RMVar_ID_117000 Human_SNP_ID_877328843 m1A Human chr9 - 136942391 136942391 136942391 AGATCCAGAACCTCAATGCCAGCACCGTCCGCACGGTGATGGTGGCCGACTGCAGCCGCTTCGAC AGATCCAGAACCTCAATGCCAGCACCGTCCGCGCGGTGATGGTGGCCGACTGCAGCCGCTTCGAC T C FBXW5 Ensembl:ENSG00000159069 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136941983..136942501 26863196 MeRIP-seq:(Medium) rs1264926854 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 1 brain Human_Splice_Rec_1101150,Human_Splice_Rec_1101178,Human_Splice_Rec_1101192,Human_Splice_Rec_1101204 RMVar_hsa_circ_81707,RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947,RMVar_hsa_circ_260948 117001 RMVar_ID_117001 Human_SNP_ID_877334977 m1A Human chr9 - 37974727 37974727 37974727 AAAGTGTTGACTCAGACTCGGAGAGCACAGTCAGCCCCCGACTGCGGGAGAGCAAGCTGCCCCAG AAAGTGTTGACTCAGACTCGGAGAGCACAGTCGGCCCCCGACTGCGGGAGAGCAAGCTGCCCCAG T C SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37974676..38068315 26863196 MeRIP-seq:(Medium) rs1268770001 Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_182813 RMVar_hsa_circ_256957,RMVar_hsa_circ_311485,RMVar_hsa_circ_291058,RMVar_hsa_circ_256958,RMVar_hsa_circ_306793,RMVar_hsa_circ_354519,RMVar_hsa_circ_367879,RMVar_hsa_circ_309307 117002 RMVar_ID_117002 Human_SNP_ID_877335107 m1A Human chr9 - 137021997 137021997 137021997 ATCTGAGCCATTCCCCCACACCTCCTAGGTCTACCACCTGCTCTTTGGTCCCTCATCTGCCCTGG ATCTGAGCCATTCCCCCACACCTCCTAGGTCTGCCACCTGCTCTTTGGTCCCTCATCTGCCCTGG T C ABCA2 Ensembl:ENSG00000107331 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137021958..137022045 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_5021380 Human_Splice_Rec_1101560,Human_Splice_Rec_1101652,Human_Splice_Rec_1101746,Human_Splice_Rec_1101838,Human_Splice_Rec_1102000,Human_Splice_Rec_1102092,Human_Splice_Rec_1102268,Human_Splice_Rec_1102302,Human_Splice_Rec_1102318,Human_Splice_Rec_1102336,Human_Splice_Rec_1102346 RMVar_hsa_circ_101033,RMVar_hsa_circ_260961 117003 RMVar_ID_117003 Human_SNP_ID_877346814 m1A Human chr9 + 85741828 85741828 85741828 CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCAGCACCTGGATCACGGCGGATCCCTCGCCGCCC CGGGGACCGCGCAGAGCCGCAGCACCCGGCTCGGCACCTGGATCACGGCGGATCCCTCGCCGCCC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:85741744..85741902 26863196 MeRIP-seq:(Medium) rs10114347 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe oligodendroglioma_Grade_II,COCA,central_nervous_system oligodendroglioma_Grade_II 5 brain GWAS_ID_7918 117004 RMVar_ID_117004 Human_SNP_ID_877350082 m1A Human chr9 - 122823084 122823084 122823084 AAAGGCTGATCAAGAAGCTGTCAATGACTTGCAGGTCCCATCTGGATGAAGAGGAGGAGCAACAG AAAGGCTGATCAAGAAGCTGTCAATGACTTGCGGGTCCCATCTGGATGAAGAGGAGGAGCAACAG T C PDCL Ensembl:ENSG00000136940 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:122822979..122823234 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 2 lung Human_RBP_ID_710929,Human_RBP_ID_1701611,Human_RBP_ID_7893555,Human_RBP_ID_9407349,Human_RBP_ID_26361062,Human_RBP_ID_27832667 Human_Splice_Rec_1078161,Human_Splice_Rec_1078167,Human_Splice_Rec_1078171 117005 RMVar_ID_117005 Human_SNP_ID_877372995 m1A Human chr9 + 136822022 136822022 136822022 TTGAGGTACCTAGGATGGGCGAGGAAATGAACAAGCTTCAGGGGAGAAGAAATGACTGTGGGAAC TTGAGGTACCTAGGATGGGCGAGGAAATGAACGAGCTTCAGGGGAGAAGAAATGACTGTGGGAAC A G AL355987.2,RABL6 Ensembl:ENSG00000272679,Ensembl:ENSG00000196642 lincRNA,Protein coding intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:136822009..136822203 26863196 MeRIP-seq:(Medium) rs1473340938 Functional Loss SNV TCGA,COSMIC 33..33 33 CESC,cervix squamous_cell_carcinoma 5 uterus Human_RBP_ID_5636918,Human_RBP_ID_16617341 Human_Splice_Rec_1100771,Human_Splice_Rec_1100799 RMVar_hsa_circ_260907,RMVar_hsa_circ_88767 117006 RMVar_ID_117006 Human_SNP_ID_877383006 m1A Human chr9 - 114504263 114504263 114504263 TCTGGTGGAACCAGGCTCTCTAGCTGAGAAGGAAGGACTGCGGGTCGGGGACCAGATTCTGCGCG TCTGGTGGAACCAGGCTCTCTAGCTGAGAAGGGAGGACTGCGGGTCGGGGACCAGATTCTGCGCG T C WHRN Ensembl:ENSG00000095397 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:114504213..114504382 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_1074405,Human_Splice_Rec_1074459,Human_Splice_Rec_1074471,Human_Splice_Rec_1074473 117007 RMVar_ID_117007 Human_SNP_ID_877387989 m1A Human chr9 + 127890901 127890901 127890901 GGGCCACGACGCGGTAGGTGGTCTTGTTGCCCACATCAGCTGAGTAGCCAGTGGTGGGTGCATCA GGGCCACGACGCGGTAGGTGGTCTTGTTGCCCGCATCAGCTGAGTAGCCAGTGGTGGGTGCATCA A G RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127890851..127890975 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 9 uterus 117008 RMVar_ID_117008 Human_SNP_ID_877396065 m1A Human chr9 + 128714350 128714350 128714350 TCGGACCCCAACAACACTGCGAGAGGCCTCTGACCCTGCCACTCCCAGGTGAGGAGCTCCCTTGC TCGGACCCCAACAACACTGCGAGAGGCCTCTGCCCCTGCCACTCCCAGGTGAGGAGCTCCCTTGC A C PKN3 Ensembl:ENSG00000160447 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128714301..128714875 26863196 MeRIP-seq:(Medium) rs770230806 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_Splice_Rec_1087695 RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587,RMVar_hsa_circ_46117,RMVar_hsa_circ_13508 117009 RMVar_ID_117009 Human_SNP_ID_877403415 m1A Human chr9 + 94459486 94459486 94459486 GCCATGGAGGGAGCCACACCCCTGGTGACTTCATGGTGCTGGATGGGAGACGCTAGCGGCATCCT GCCATGGAGGGAGCCACACCCCTGGTGACTTCGTGGTGCTGGATGGGAGACGCTAGCGGCATCCT A G MFSD14B Ensembl:ENSG00000148110 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:94458459..94459602 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_722455,Human_RBP_ID_7949070 117010 RMVar_ID_117010 Human_SNP_ID_877410821 m1A Human chr9 + 126805069 126805069 126805069 GCTGAATCTGTTGCGGCAGCTGAGGCTACAACAGGCCTGCGCCGGCGGCAGAGAGGATATCTTGG GCTGAATCTGTTGCGGCAGCTGAGGCTACAACCGGCCTGCGCCGGCGGCAGAGAGGATATCTTGG A C ZBTB43 Ensembl:ENSG00000169155 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:126805034..126805186 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_18427386,Human_RBP_ID_19025586 Human_Splice_Rec_1081171,Human_Splice_Rec_1081173,Human_Splice_Rec_1081175 RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 117011 RMVar_ID_117011 Human_SNP_ID_877429113 m1A Human chr9 + 87525479 87525479 87525479 AGGATATCGGTTTCATTAAGTTGGACTAAATGATCTTCCTTCAAAGGATTATCCAAGGCATATAC AGGATATCGGTTTCATTAAGTTGGACTAAATGCTCTTCCTTCAAAGGATTATCCAAGGCATATAC A C DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs879184341 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,pancreas ductal_carcinoma 8 pancreas Human_RBP_ID_26566869 RMVar_hsa_circ_257632,RMVar_hsa_circ_122387,RMVar_hsa_circ_349031,RMVar_hsa_circ_373594,RMVar_hsa_circ_337567,RMVar_hsa_circ_70360,RMVar_hsa_circ_257633,RMVar_hsa_circ_257634,RMVar_hsa_circ_257631 117012 RMVar_ID_117012 Human_SNP_ID_877429254 m1A Human chr9 - 125915650 125915650 125915650 CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGAAGCGAGAAACAGAGGACAAATAGTGTGAGTAT CAAGGAAAGAGAGAGAGAGACAGAGAGAGAAGGAGCGAGAAACAGAGGACAAATAGTGTGAGTAT T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:125915644..125915729 26863196 MeRIP-seq:(Medium) rs138144415 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 4 head and neck 117013 RMVar_ID_117013 Human_SNP_ID_877433904 m1A Human chr9 - 26892703 26892703 26892703 ATGGTTGCAGCAGAGGGATCATGACGGGGAAAAAGTCCTCCCGGGAGAAACGGCGCAAACGTAGC ATGGTTGCAGCAGAGGGATCATGACGGGGAAAGAGTCCTCCCGGGAGAAACGGCGCAAACGTAGC T C CAAP1 Ensembl:ENSG00000120159 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:26892457..26892800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_5036111,Human_RBP_ID_18134325,Human_RBP_ID_22119801,Human_RBP_ID_22339477 117014 RMVar_ID_117014 Human_SNP_ID_877441713 m1A Human chr9 - 15422910 15422910 15422910 GACTGGGTCCTGCCTGCCACCCACCCCGCTACACGTAGGGCCACCTCGGCTTCCTTCAGCCATGT GACTGGGTCCTGCCTGCCACCCACCCCGCTACCCGTAGGGCCACCTCGGCTTCCTTCAGCCATGT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:15422851..15423950;chr9:15422851..15423135;chr9:15422851..15423127;chr9:15422851..15423153 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 2 stomach 117015 RMVar_ID_117015 Human_SNP_ID_877446187 m1A Human chr9 - 21971162 21971162 21971162 CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAACTGCGCCGACCCCGCCA CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCGCGGCGCGGAGCCCAACTGCGCCGACCCCGCCA T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970995..21971204 26863196 MeRIP-seq:(Medium) rs756750256 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,pancreas pancreatoblastoma,pancreas ductal_carcinoma,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia,ovary serous_carcinoma 41 ovary,pancreas,haematopoietic and lymphoid tissue Human_RBP_ID_717039,Human_RBP_ID_5042037,Human_RBP_ID_8702224,Human_RBP_ID_18134013,Human_RBP_ID_24297452,Human_RBP_ID_24523182,Human_RBP_ID_27135409,Human_RBP_ID_27374365 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Clinvar_Rec_181,Clinvar_Rec_182 117016 RMVar_ID_117016 Human_SNP_ID_877446192 m1A Human chr9 - 21971162 21971162 21971162 CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAACTGCGCCGACCCCGCCA CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCCCGGCGCGGAGCCCAACTGCGCCGACCCCGCCA T G CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970995..21971204 26863196 MeRIP-seq:(Medium) rs756750256 Functional Loss SNV COSMIC 33..33 33 oesophagus Barrett_oesophagus 10 oesophagus Human_RBP_ID_717039,Human_RBP_ID_5042037,Human_RBP_ID_8702224,Human_RBP_ID_18134013,Human_RBP_ID_24297452,Human_RBP_ID_24523182,Human_RBP_ID_27135409,Human_RBP_ID_27374365 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Clinvar_Rec_181,Clinvar_Rec_182 117017 RMVar_ID_117017 Human_SNP_ID_877446202 m1A Human chr9 - 21971162 21971162 21971162 CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCACGGCGCGGAGCCCAACTGCGCCGACCCCGCCA CAGCGCCCGAGTGGCGGAGCTGCTGCTGCTCCTCGGCGCGGAGCCCAACTGCGCCGACCCCGCCA T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970995..21971204 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 face squamous_cell_carcinoma,skin squamous_cell_carcinoma 10 skin,head and neck Human_RBP_ID_717039,Human_RBP_ID_5042037,Human_RBP_ID_8702224,Human_RBP_ID_18134013,Human_RBP_ID_24297452,Human_RBP_ID_24523182,Human_RBP_ID_27135409,Human_RBP_ID_27374365 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 117018 RMVar_ID_117018 Human_SNP_ID_877450840 m1A Human chr9 + 71684702 71684702 71684702 GGGCCTGAGTTGCCACTTAAAACTGTCATTCAATATCATAGAAAATCCTCAAAGGCTGCCCAGAA GGGCCTGAGTTGCCACTTAAAACTGTCATTCACTATCATAGAAAATCCTCAAAGGCTGCCCAGAA A C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:71684656..71684825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary 117019 RMVar_ID_117019 Human_SNP_ID_877457539 m1A Human chr9 - 131430062 131430062 131430062 TCTGCCTTTGAAATAGAGAAGAAAAAAAAAAAAAGAGAGAGAAAAAAAAAAAAGAGTGTCACTAC TCTGCCTTTGAAATAGAGAAGAAAAAAAAAAAGAGAGAGAGAAAAAAAAAAAAGAGTGTCACTAC T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131430056..131430200 26863196 MeRIP-seq:(Medium) rs76644652 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,COCA,large_intestine adenocarcinoma 8 ovary,large intestine 117020 RMVar_ID_117020 Human_SNP_ID_877460100 m1A Human chr9 + 17135230 17135230 17135230 GCGCGGGAGGTGGTCGCGGACGAAAGTGATAAAATCTGGGTGGGTGAAGAAGGGTCAGGGGGCCG GCGCGGGAGGTGGTCGCGGACGAAAGTGATAACATCTGGGTGGGTGAAGAAGGGTCAGGGGGCCG A C CNTLN Ensembl:ENSG00000044459 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:17135065..17135383 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_92231,Human_RBP_ID_18133355,Human_RBP_ID_19023715 117021 RMVar_ID_117021 Human_SNP_ID_877470085 m1A Human chr9 - 133350020 133350020 133350020 CTGCTCGAAGGACAGGTGGTCTCTTCGTTGGGACGTCCCCTTTGCCAGCAGCCTTCTTCTCGGCC CTGCTCGAAGGACAGGTGGTCTCTTCGTTGGGGCGTCCCCTTTGCCAGCAGCCTTCTTCTCGGCC T C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:133349956..133350098 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 PBCA,UCEC 2 - 117022 RMVar_ID_117022 Human_SNP_ID_877480022 m1A Human chr9 - 21974799 21974798 21974799 CAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCCACGGCCGCGG CAGCATGGAGCCGGCGGCGGGGAGCAGCATGG_GCCTTCGGCTGACTGGCTGGCCACGGCCGCGG CT C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:21974576..21974950 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_92522,Human_RBP_ID_717045 117023 RMVar_ID_117023 Human_SNP_ID_877496122 m1A Human chr9 - 130579648 130579648 130579648 TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGACGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC TACCGCCCCCGCCGCCGTCGCCGCCGCCGCCGCCGCCGCCGACGCCGCCGCTCGGCTCCCCGGTC T G RF00017-4620 RNACentral:URS000092122F SRP RNA intron GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:130579601..130579755 26863196 MeRIP-seq:(Medium) rs1207238854 Functional Loss SNV ICGC 33..33 33 STAD 1 - 117024 RMVar_ID_117024 Human_SNP_ID_877497044 m1A Human chr9 + 5054776 5054776 5054776 TACACAGAGAAATTTGAAGTAAAAGAACCTGGAAGTGGTCCTTCAGGTGAGGAGATTTTTGCAAC TACACAGAGAAATTTGAAGTAAAAGAACCTGGGAGTGGTCCTTCAGGTGAGGAGATTTTTGCAAC A G JAK2 Ensembl:ENSG00000096968 Protein coding CDS GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:5054760..5054847 26863410 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_759,RMVar_hsa_circ_19998,RMVar_hsa_circ_293467,RMVar_hsa_circ_335183,RMVar_hsa_circ_367185,RMVar_hsa_circ_344758,RMVar_hsa_circ_313932,RMVar_hsa_circ_309944,RMVar_hsa_circ_56133,RMVar_hsa_circ_293077,RMVar_hsa_circ_94446,RMVar_hsa_circ_255461,RMVar_hsa_circ_255463,RMVar_hsa_circ_255462,RMVar_hsa_circ_255459,RMVar_hsa_circ_255460,RMVar_hsa_circ_255458,RMVar_hsa_circ_363968,RMVar_hsa_circ_255466,RMVar_hsa_circ_255467,RMVar_hsa_circ_9228,RMVar_hsa_circ_15643,RMVar_hsa_circ_255472,RMVar_hsa_circ_305875,RMVar_hsa_circ_332947,RMVar_hsa_circ_255471 117025 RMVar_ID_117025 Human_SNP_ID_877498197 m1A Human chr9 + 137214677 137214677 137214677 GGGCCTGGACCCTGACCAGCTCTTCATGCTGCAGCCGCGGGAGCCAGGTGAGCCCAGCCTCGGCC GGGCCTGGACCCTGACCAGCTCTTCATGCTGCTGCCGCGGGAGCCAGGTGAGCCCAGCCTCGGCC A T NDOR1 Ensembl:ENSG00000188566 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:137214626..137214700 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 4 lung Human_RBP_ID_19026315 Human_Splice_Rec_1103283,Human_Splice_Rec_1103297,Human_Splice_Rec_1103325,Human_Splice_Rec_1103351 Human_miRNA_ID_795976,Human_miRNA_ID_1937286,Human_miRNA_ID_1948386 RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153,RMVar_hsa_circ_96901,RMVar_hsa_circ_264898,RMVar_hsa_circ_261003,RMVar_hsa_circ_348016 117026 RMVar_ID_117026 Human_SNP_ID_877506792 m1A Human chr9 - 136909981 136909981 136909981 GGAGGTGAAGGACACTCACCTTCTCCCGGGGGATCTTCTTCTTGCCGCAGCCGTCACAAGTTAAG GGAGGTGAAGGACACTCACCTTCTCCCGGGGGTTCTTCTTCTTGCCGCAGCCGTCACAAGTTAAG T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136902389..136920444 32194978 MeRIP-seq:(Medium) rs1250915147 Functional Loss SNV TCGA 33..33 33 SKCM 1 - 117027 RMVar_ID_117027 Human_SNP_ID_877517689 m1A Human chr9 + 136395373 136395373 136395373 CCCATGTATGTGCTTGGGGGCAGGCTTTTGCCATCTTTCACCTTGGTGCCTTTGGACCCAGCCAG CCCATGTATGTGCTTGGGGGCAGGCTTTTGCCGTCTTTCACCTTGGTGCCTTTGGACCCAGCCAG A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136395322..136397008 32194978 MeRIP-seq:(Medium) rs4266763 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,rectum adenocarcinoma,liver neoplasm,large_intestine adenocarcinoma 3 liver,large intestine Clinvar_Rec_538 GWAS_ID_12296,GWAS_ID_12297,GWAS_ID_12298,GWAS_ID_12299,GWAS_ID_12300,GWAS_ID_12301,GWAS_ID_12302,GWAS_ID_12303,GWAS_ID_12304,GWAS_ID_12305,GWAS_ID_12306,GWAS_ID_12307,GWAS_ID_12308,GWAS_ID_12309,GWAS_ID_12310,GWAS_ID_12311,GWAS_ID_12312,GWAS_ID_12313,GWAS_ID_12314,GWAS_ID_12315,GWAS_ID_12316,GWAS_ID_12317,GWAS_ID_12318,GWAS_ID_12319,GWAS_ID_12320,GWAS_ID_12321,GWAS_ID_12322,GWAS_ID_12323,GWAS_ID_12324,GWAS_ID_12325,GWAS_ID_12326,GWAS_ID_12327,GWAS_ID_12328,GWAS_ID_12329,GWAS_ID_12330,GWAS_ID_12331,GWAS_ID_12332,GWAS_ID_12333,GWAS_ID_12334,GWAS_ID_12335,GWAS_ID_12336,GWAS_ID_12337,GWAS_ID_12338,GWAS_ID_12339,GWAS_ID_12340,GWAS_ID_12341,GWAS_ID_12342,GWAS_ID_12343,GWAS_ID_12344,GWAS_ID_12345,GWAS_ID_12346,GWAS_ID_12347,GWAS_ID_12348,GWAS_ID_12349,GWAS_ID_12350,GWAS_ID_12351,GWAS_ID_12352,GWAS_ID_12353,GWAS_ID_12354,GWAS_ID_12355,GWAS_ID_12356,GWAS_ID_12357,GWAS_ID_12358,GWAS_ID_12359,GWAS_ID_12360,GWAS_ID_12361,GWAS_ID_12362,GWAS_ID_12363,GWAS_ID_12364,GWAS_ID_12365,GWAS_ID_12366,GWAS_ID_12367,GWAS_ID_12368,GWAS_ID_12369,GWAS_ID_12370,GWAS_ID_12371,GWAS_ID_12372,GWAS_ID_12373,GWAS_ID_12374,GWAS_ID_12375,GWAS_ID_12376,GWAS_ID_12377,GWAS_ID_12378,GWAS_ID_12379,GWAS_ID_12380,GWAS_ID_12381,GWAS_ID_12382,GWAS_ID_12383,GWAS_ID_12384,GWAS_ID_12385,GWAS_ID_12386,GWAS_ID_12387,GWAS_ID_12388,GWAS_ID_12389,GWAS_ID_12390,GWAS_ID_12391,GWAS_ID_12392,GWAS_ID_12393,GWAS_ID_12394,GWAS_ID_12395,GWAS_ID_12396,GWAS_ID_12397,GWAS_ID_12398,GWAS_ID_12399,GWAS_ID_12400,GWAS_ID_12401,GWAS_ID_12402,GWAS_ID_12403,GWAS_ID_12404,GWAS_ID_12405,GWAS_ID_12406,GWAS_ID_12407,GWAS_ID_12408,GWAS_ID_12409,GWAS_ID_12410,GWAS_ID_12411,GWAS_ID_12412,GWAS_ID_12413,GWAS_ID_12414,GWAS_ID_12415,GWAS_ID_12416,GWAS_ID_12417,GWAS_ID_12418,GWAS_ID_12419,GWAS_ID_12420,GWAS_ID_12421,GWAS_ID_12422,GWAS_ID_12423,GWAS_ID_12424,GWAS_ID_12425,GWAS_ID_12426,GWAS_ID_12427,GWAS_ID_12428,GWAS_ID_12429,GWAS_ID_12430,GWAS_ID_12431,GWAS_ID_12432,GWAS_ID_12433,GWAS_ID_12434,GWAS_ID_12435,GWAS_ID_12436,GWAS_ID_12437,GWAS_ID_12438,GWAS_ID_12439,GWAS_ID_12440,GWAS_ID_12441,GWAS_ID_12442,GWAS_ID_12443,GWAS_ID_12444,GWAS_ID_12445,GWAS_ID_12446,GWAS_ID_12447,GWAS_ID_12448,GWAS_ID_12449,GWAS_ID_12450,GWAS_ID_12451,GWAS_ID_12452,GWAS_ID_12453,GWAS_ID_12454,GWAS_ID_12455,GWAS_ID_12456,GWAS_ID_12457,GWAS_ID_12458,GWAS_ID_12459,GWAS_ID_12460,GWAS_ID_12461 117028 RMVar_ID_117028 Human_SNP_ID_877520547 m1A Human chr9 - 70259017 70259017 70259017 TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCCAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70258972..70259151 26863196 MeRIP-seq:(Medium) rs878983240 Functional Loss SNV TCGA 33..33 33 BRCA 1 - 117029 RMVar_ID_117029 Human_SNP_ID_877528536 m1A Human chr9 - 128166276 128166276 128166276 CAGCGGCCGCCCACCCTCCCAGCCCAACACCCAGGACAAAACACCCAGCAAGGTGACGGCTCGAC CAGCGGCCGCCCACCCTCCCAGCCCAACACCCCGGACAAAACACCCAGCAAGGTGACGGCTCGAC T G CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated chr9:128166153..128166325;chr9:128166226..128166350 26863196 MeRIP-seq:(Medium) rs1376182147 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_17437215,Human_RBP_ID_26834320 Human_Splice_Rec_1084681 Human_miRNA_ID_255964,Human_miRNA_ID_656305,Human_miRNA_ID_2039888,Human_miRNA_ID_2254778,Human_miRNA_ID_3018869 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 117030 RMVar_ID_117030 Human_SNP_ID_877538289 m1A Human chr9 + 127714683 127714683 127714683 AGCTCATCATGCACCAGGTAGACTTCCTCGGCAGTCAGCCCAAACAGCTCCGCTTAGCACAGGGA AGCTCATCATGCACCAGGTAGACTTCCTCGGCTGTCAGCCCAAACAGCTCCGCTTAGCACAGGGA A T CFAP157 Ensembl:ENSG00000160401 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127714615..127714765 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 117031 RMVar_ID_117031 Human_SNP_ID_877550144 m1A Human chr9 - 33258941 33258941 33258941 AAGATAGCTGACCAGCTGGAAGAGTTGAATAAAGAGCTTACTGGAATCCAGCAGGTAACTCTCTT AAGATAGCTGACCAGCTGGAAGAGTTGAATAAGGAGCTTACTGGAATCCAGCAGGTAACTCTCTT T C BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_962001,Human_RBP_ID_9351877,Human_RBP_ID_9406844,Human_RBP_ID_18135037,Human_RBP_ID_26360626,Human_RBP_ID_27832317 Human_Splice_Rec_1038034,Human_Splice_Rec_1038035,Human_Splice_Rec_1038041,Human_Splice_Rec_1038048,Human_Splice_Rec_1038049,Human_Splice_Rec_1038060,Human_Splice_Rec_1038061,Human_Splice_Rec_1038074,Human_Splice_Rec_1038075,Human_Splice_Rec_1038084,Human_Splice_Rec_1038085,Human_Splice_Rec_1038092 RMVar_hsa_circ_57336,RMVar_hsa_circ_312814,RMVar_hsa_circ_347903,RMVar_hsa_circ_306598 117032 RMVar_ID_117032 Human_SNP_ID_877555942 m1A Human chr9 + 133360355 133360355 133360355 CTTTTTGACAGACAAAGAGGATGAGAAGGCAAAGCCCCCAAGAGAGAAGGCCACTGATGAGGGCA CTTTTTGACAGACAAAGAGGATGAGAAGGCAACGCCCCCAAGAGAGAAGGCCACTGATGAGGGCA A C SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Normoxia;HTR8/Svneo,Hypoxia IP chr9:133360307..133361121;chr9:133360307..133361073 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_Splice_Rec_1095620,Human_Splice_Rec_1095621 117033 RMVar_ID_117033 Human_SNP_ID_877566255 m1A Human chr9 - 83661554 83661554 83661554 CTACTGCATGCATCACTTCTGCATTTATTGTAATTTTTTAAAAACATCACCTTTTATAGTTGGGT CTACTGCATGCATCACTTCTGCATTTATTGTATTTTTTTAAAAACATCACCTTTTATAGTTGGGT T A UBQLN1 Ensembl:ENSG00000135018 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:83661355..83661555 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_720987,Human_RBP_ID_2065818,Human_RBP_ID_7940422,Human_RBP_ID_16718028,Human_RBP_ID_17436738,Human_RBP_ID_17550288,Human_RBP_ID_17716815,Human_RBP_ID_18138447,Human_RBP_ID_21906443,Human_RBP_ID_22838841,Human_RBP_ID_23093447,Human_RBP_ID_23300376,Human_RBP_ID_24442960,Human_RBP_ID_27787167 Human_miRNA_ID_860016 RMVar_hsa_circ_257402,RMVar_hsa_circ_100458,RMVar_hsa_circ_114557,RMVar_hsa_circ_257396,RMVar_hsa_circ_257397,RMVar_hsa_circ_257398,RMVar_hsa_circ_106466,RMVar_hsa_circ_268524,RMVar_hsa_circ_82923,RMVar_hsa_circ_84247,RMVar_hsa_circ_78767,RMVar_hsa_circ_257403,RMVar_hsa_circ_257400,RMVar_hsa_circ_257401,RMVar_hsa_circ_257399 117034 RMVar_ID_117034 Human_SNP_ID_877574280 m1A Human chr9 - 93577170 93577170 93577170 CCCAGCTGACAGGCGGCCCGGCCCGGGCCTGGAGCCCCAACTTCCCCGCGCCCCGAGCCCCGAGC CCCAGCTGACAGGCGGCCCGGCCCGGGCCTGGGGCCCCAACTTCCCCGCGCCCCGAGCCCCGAGC T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:93577163..93577386;chr9:93577138..93577342 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 117035 RMVar_ID_117035 Human_SNP_ID_877578048 m1A Human chr9 - 21971111 21971111 21971111 CGCCGACCCCGCCACTCTCACCCGACCCGTGCACGACGCTGCCCGGGAGGGCTTCCTGGACACGC CGCCGACCCCGCCACTCTCACCCGACCCGTGCGCGACGCTGCCCGGGAGGGCTTCCTGGACACGC T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:21970877..21971278;chr9:21970868..21971254 26863196 MeRIP-seq:(Medium) rs1057519881 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,kidney clear_cell_renal_cell_carcinoma,SKCM,colon adenocarcinoma,ovary mucinous_carcinoma,HNSC,oesophagus adenocarcinoma,head_neck squamous_cell_carcinoma,ESCA,large_intestine adenocarcinoma 63 lung,kidney,ovary,oesophagus,head and neck,large intestine Human_RBP_ID_717038,Human_RBP_ID_8275220,Human_RBP_ID_18134011,Human_RBP_ID_18212440,Human_RBP_ID_24297451,Human_RBP_ID_27545288 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1549725,Human_miRNA_ID_1549902,Human_miRNA_ID_1550232 Clinvar_Rec_180 117036 RMVar_ID_117036 Human_SNP_ID_877578054 m1A Human chr9 - 21971111 21971111 21971111 CGCCGACCCCGCCACTCTCACCCGACCCGTGCACGACGCTGCCCGGGAGGGCTTCCTGGACACGC CGCCGACCCCGCCACTCTCACCCGACCCGTGCCCGACGCTGCCCGGGAGGGCTTCCTGGACACGC T G CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:21970877..21971278;chr9:21970868..21971254 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,LICA,liver neoplasm,liver hepatocellular_carcinoma 41 liver,pancreas Human_RBP_ID_717038,Human_RBP_ID_8275220,Human_RBP_ID_18134011,Human_RBP_ID_18212440,Human_RBP_ID_24297451,Human_RBP_ID_27545288 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1549725,Human_miRNA_ID_1549902,Human_miRNA_ID_1550232 117037 RMVar_ID_117037 Human_SNP_ID_877578056 m1A Human chr9 - 21971111 21971111 21971111 CGCCGACCCCGCCACTCTCACCCGACCCGTGCACGACGCTGCCCGGGAGGGCTTCCTGGACACGC CGCCGACCCCGCCACTCTCACCCGACCCGTGCTCGACGCTGCCCGGGAGGGCTTCCTGGACACGC T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:21970877..21971278;chr9:21970868..21971254 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 12 lung Human_RBP_ID_717038,Human_RBP_ID_8275220,Human_RBP_ID_18134011,Human_RBP_ID_18212440,Human_RBP_ID_24297451,Human_RBP_ID_27545288 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1549725,Human_miRNA_ID_1549902,Human_miRNA_ID_1550232 117038 RMVar_ID_117038 Human_SNP_ID_877579490 m1A Human chr9 - 134812670 134812670 134812670 ACTGCACCAGGGTTTCCTATTCCACCTGGGGGACCTTGTGGGCCATCAGCACCTGGAGCTCCGGA ACTGCACCAGGGTTTCCTATTCCACCTGGGGGTCCTTGTGGGCCATCAGCACCTGGAGCTCCGGA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134812406..134812762 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 117039 RMVar_ID_117039 Human_SNP_ID_877590812 m1A Human chr9 - 128633391 128633391 128633391 ACAGTGGAAAGTGAGAGCACACAGAGGAGCGGACATGCAGCAAGGCGACGCAGGGCAAGCAGCGA ACAGTGGAAAGTGAGAGCACACAGAGGAGCGGGCATGCAGCAAGGCGACGCAGGGCAAGCAGCGA T C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128633376..128633400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - Human_RBP_ID_16585623 117040 RMVar_ID_117040 Human_SNP_ID_877595606 m1A Human chr9 - 137113002 137113002 137113002 GAATGCCTTCACCGTGCTGGCCATGATGGACTACCCCTACCCCACTGACTTCCTGGGTCCCCTCC GAATGCCTTCACCGTGCTGGCCATGATGGACTGCCCCTACCCCACTGACTTCCTGGGTCCCCTCC T C DPP7 Ensembl:ENSG00000176978 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:137112953..137113064 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_91804,Human_RBP_ID_797976,Human_RBP_ID_3975240,Human_RBP_ID_16619454,Human_RBP_ID_22338379,Human_RBP_ID_27544688 Human_Splice_Rec_1102699,Human_Splice_Rec_1102723,Human_Splice_Rec_1102735,Human_Splice_Rec_1102763,Human_Splice_Rec_1102777,Human_Splice_Rec_1102783 RMVar_hsa_circ_90241,RMVar_hsa_circ_115463,RMVar_hsa_circ_260979,RMVar_hsa_circ_126416,RMVar_hsa_circ_260983,RMVar_hsa_circ_8046,RMVar_hsa_circ_93603,RMVar_hsa_circ_260984,RMVar_hsa_circ_260985 117041 RMVar_ID_117041 Human_SNP_ID_877598071 m1A Human chr9 + 133360399 133360399 133360399 AGAAGGCCACTGATGAGGGCAGGAGAGAGACGACCGTGTACCGAGGGCTGGTCCAGAAGCGCGGG AGAAGGCCACTGATGAGGGCAGGAGAGAGACGCCCGTGTACCGAGGGCTGGTCCAGAAGCGCGGG A C SURF2 Ensembl:ENSG00000148291 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:133357797..133361150 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_Splice_Rec_1095621 117042 RMVar_ID_117042 Human_SNP_ID_877604389 m1A Human chr9 - 62799589 62799589 62799589 TCCACCTTGCTCTCTCTCTCTCTCTCTCTCTCAATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA TCCACCTTGCTCTCTCTCTCTCTCTCTCTCTCTATCTCCCCAGTTCCTCTCTGTCTCTCTCTCCA T A lnc-FOXD4L5-27,lnc-FOXD4L5-27:2 RNACentral:URS00008C163A,RNACentral:URS00009AE1AE lincRNA,lincRNA intron,intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7032037 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_1118736 117043 RMVar_ID_117043 Human_SNP_ID_877604406 m1A Human chr9 - 127980555 127980555 127980555 GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCCAGCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG GGGGCCGCCCTCCGCCCTCAGCCTTACCGGCCCGCCAGCCCGCCCGCCGCCCTCAGTCTCACCGG T G FAM102A Ensembl:ENSG00000167106 Protein coding 5'UTR GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:127980453..127980673 26863410 MeRIP-seq:(Medium) rs113481265 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_5454176 Clinvar_Rec_689 GWAS_ID_14726,GWAS_ID_14727,GWAS_ID_14728,GWAS_ID_14729 117044 RMVar_ID_117044 Human_SNP_ID_877605563 m1A Human chr9 + 121332545 121332545 121332545 TCCCTCCTTTGTGGGCTGGTTCCTTGGCTGGGATGATGATTACTGGTCTGTGGACCCCTTGGACA TCCCTCCTTTGTGGGCTGGTTCCTTGGCTGGGGTGATGATTACTGGTCTGTGGACCCCTTGGACA A G GSN Ensembl:ENSG00000148180 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:121332495..121332735 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 3 - Human_RBP_ID_964964,Human_RBP_ID_17666555,Human_RBP_ID_18128760,Human_RBP_ID_22466178,Human_RBP_ID_22777020,Human_RBP_ID_23216712 RMVar_hsa_circ_92500,RMVar_hsa_circ_75677,RMVar_hsa_circ_259203,RMVar_hsa_circ_259204 117045 RMVar_ID_117045 Human_SNP_ID_877605921 m1A Human chr9 + 97922328 97922328 97922328 GTAGGTAAAAGAATGACGCACGTCAGTTCCAGATCGTGCGTTTTACACCCCTCTCGGCAACGAAG GTAGGTAAAAGAATGACGCACGTCAGTTCCAGGTCGTGCGTTTTACACCCCTCTCGGCAACGAAG A G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:97922325..97922479 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas acinar_carcinoma 2 pancreas 117046 RMVar_ID_117046 Human_SNP_ID_877614120 m1A Human chr9 - 137113113 137113113 137113113 TTCAAGTCTCTGCCCCTTCCACGCAGCCTACGACACGGTCCGCTGGGAGTTCGGCACCTGCCAGC TTCAAGTCTCTGCCCCTTCCACGCAGCCTACGGCACGGTCCGCTGGGAGTTCGGCACCTGCCAGC T C DPP7 Ensembl:ENSG00000176978 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137112929..137113114 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_256318,Human_RBP_ID_23216789,Human_RBP_ID_26362408 Human_Splice_Rec_1102698,Human_Splice_Rec_1102722,Human_Splice_Rec_1102762,Human_Splice_Rec_1102776,Human_Splice_Rec_1102782,Human_Splice_Rec_1102788,Human_Splice_Rec_1102798 RMVar_hsa_circ_90241,RMVar_hsa_circ_115463,RMVar_hsa_circ_260979,RMVar_hsa_circ_126416,RMVar_hsa_circ_260983,RMVar_hsa_circ_8046,RMVar_hsa_circ_93603,RMVar_hsa_circ_260984,RMVar_hsa_circ_260985 117047 RMVar_ID_117047 Human_SNP_ID_877621542 m1A Human chr9 + 137107809 137107809 137107809 GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACACTGCAGCTTGGGGGCCCTGGCATCCCCATCCC GGGCGGGCTTGCCGCAGCCTCGGGGTGGCCACGCTGCAGCTTGGGGGCCCTGGCATCCCCATCCC A G MAN1B1 Ensembl:ENSG00000177239 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs11790092 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_3975234,Human_RBP_ID_5410649,Human_RBP_ID_9339339,Human_RBP_ID_18414476 RMVar_hsa_circ_90773,RMVar_hsa_circ_260978 117048 RMVar_ID_117048 Human_SNP_ID_877625255 m1A Human chr9 - 133762492 133762492 133762492 CTGCGGCCCAGCAGGCGCGGAGGATGGCGGGGAGGAAGCCAGCAGCCCCTGTGTTTACTGTCGTC CTGCGGCCCAGCAGGCGCGGAGGATGGCGGGGTGGAAGCCAGCAGCCCCTGTGTTTACTGTCGTC T A VAV2 Ensembl:ENSG00000160293 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Hypoxia IP chr9:133762441..133762805;chr9:133762441..133762542 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus Human_RBP_ID_1119209,Human_RBP_ID_5106983 RMVar_hsa_circ_268841 117049 RMVar_ID_117049 Human_SNP_ID_877659228 m1A Human chr9 - 124908412 124908412 124908412 ATACCAGACAACAGCTCTTGGCAGCCAGAAGCAGCCAGGCTAAGGCCATTAACACCCTGGAGACT ATACCAGACAACAGCTCTTGGCAGCCAGAAGCGGCCAGGCTAAGGCCATTAACACCCTGGAGACT T C GOLGA1 Ensembl:ENSG00000136935 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:124908408..124908576 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_963764,Human_RBP_ID_3974773,Human_RBP_ID_9407383,Human_RBP_ID_26361095,Human_RBP_ID_27832688 Human_Splice_Rec_1079746,Human_Splice_Rec_1079747,Human_Splice_Rec_1079780,Human_Splice_Rec_1079781,Human_Splice_Rec_1079808,Human_Splice_Rec_1079809,Human_Splice_Rec_1079820,Human_Splice_Rec_1079821 RMVar_hsa_circ_89330,RMVar_hsa_circ_259485,RMVar_hsa_circ_259484,RMVar_hsa_circ_259486,RMVar_hsa_circ_72408,RMVar_hsa_circ_50603,RMVar_hsa_circ_99632,RMVar_hsa_circ_259488,RMVar_hsa_circ_259489,RMVar_hsa_circ_109956,RMVar_hsa_circ_304445,RMVar_hsa_circ_358528,RMVar_hsa_circ_259493,RMVar_hsa_circ_259491,RMVar_hsa_circ_267397,RMVar_hsa_circ_111604,RMVar_hsa_circ_9047,RMVar_hsa_circ_264960,RMVar_hsa_circ_344722,RMVar_hsa_circ_367396,RMVar_hsa_circ_271054,RMVar_hsa_circ_259494,RMVar_hsa_circ_259495 117050 RMVar_ID_117050 Human_SNP_ID_877659335 m1A Human chr9 - 89001162 89001162 89001162 GCATTCACAGACGATTAGCTCCAAAATCCACGAGAGGGCGCCCCAGGAACATTCATTTCAAAGGG GCATTCACAGACGATTAGCTCCAAAATCCACGGGAGGGCGCCCCAGGAACATTCATTTCAAAGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89001111..89001215 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 12 stomach 117051 RMVar_ID_117051 Human_SNP_ID_877660091 m1A Human chr9 - 113408842 113408840 113408843 TGATGAAGACGAAGAAAGGCTGGAAGAAGAAGAACAGAATGAAGAGGAAGAAGTAGACAACTGAA TGATGAAGACGAAGAAAGGCTGGAAGAAGAA___CAGAATGAAGAGGAAGAAGTAGACAACTGAA GTTC G POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:113408701..113409756;chr9:113408651..113409675;chr9:113408676..113409727 26863196 MeRIP-seq:(Medium) rs761315806 Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_92543,Human_RBP_ID_219732,Human_RBP_ID_1701281,Human_RBP_ID_2059673,Human_RBP_ID_3184550,Human_RBP_ID_7890335,Human_RBP_ID_9407210,Human_RBP_ID_16547450,Human_RBP_ID_17666341,Human_RBP_ID_18541896,Human_RBP_ID_18545071,Human_RBP_ID_22334552,Human_RBP_ID_23094347,Human_RBP_ID_23117259,Human_RBP_ID_24549634,Human_RBP_ID_24555416,Human_RBP_ID_26360976,Human_RBP_ID_27129234,Human_RBP_ID_27832609 117052 RMVar_ID_117052 Human_SNP_ID_877674492 m1A Human chr9 + 87632378 87632378 87632378 ACATATGTAGGGATGAAGGAGGATGAGTGCATATGTAGAAATGAAGGAAGATGGGTATACATGTA ACATATGTAGGGATGAAGGAGGATGAGTGCATTTGTAGAAATGAAGGAAGATGGGTATACATGTA A T DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:87632247..87632634 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_24311470 RMVar_hsa_circ_54757,RMVar_hsa_circ_257632,RMVar_hsa_circ_122387,RMVar_hsa_circ_349031,RMVar_hsa_circ_373594,RMVar_hsa_circ_337567,RMVar_hsa_circ_257633,RMVar_hsa_circ_60330,RMVar_hsa_circ_257631,RMVar_hsa_circ_55453,RMVar_hsa_circ_8862,RMVar_hsa_circ_36832 117053 RMVar_ID_117053 Human_SNP_ID_877674825 m1A Human chr9 + 87632378 87632378 87632378 ACATATGTAGGGATGAAGGAGGATGAGTGCATATGTAGAAATGAAGGAAGATGGGTATACATGTA ACATATGTAGGGATGAAGGAGGATGAGTGCATGTGTAGAAATGAAGGAAGATGGGTATACATGTA A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:87632247..87632634 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_24311470 RMVar_hsa_circ_54757,RMVar_hsa_circ_257632,RMVar_hsa_circ_122387,RMVar_hsa_circ_349031,RMVar_hsa_circ_373594,RMVar_hsa_circ_337567,RMVar_hsa_circ_257633,RMVar_hsa_circ_60330,RMVar_hsa_circ_257631,RMVar_hsa_circ_55453,RMVar_hsa_circ_8862,RMVar_hsa_circ_36832 117054 RMVar_ID_117054 Human_SNP_ID_877685453 m1A Human chr9 + 131523156 131523156 131523156 GAACACCCGTGCTGGGGTCGGGATGAGGTTGAAGGGTCTTGGTCAATGTACGTAATGAGCAGGGT GAACACCCGTGCTGGGGTCGGGATGAGGTTGACGGGTCTTGGTCAATGTACGTAATGAGCAGGGT A C POMT1 Ensembl:ENSG00000130714 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:131523107..131523203 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCM 1 - Human_RBP_ID_713873,Human_RBP_ID_18131326,Human_RBP_ID_18905162,Human_RBP_ID_23216754,Human_RBP_ID_26566624 117055 RMVar_ID_117055 Human_SNP_ID_877688770 m1A Human chr9 + 95060751 95060751 95060751 TTCTGGAGCATCTCTTGGAGCAGAAGACTCTGAGCCCCCGAACTCTGCAAAGCCTCCAGAGGACA TTCTGGAGCATCTCTTGGAGCAGAAGACTCTGGGCCCCCGAACTCTGCAAAGCCTCCAGAGGACA A G AOPEP Ensembl:ENSG00000148120 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:95060636..95060750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_963379,Human_RBP_ID_9407072,Human_RBP_ID_19025153,Human_RBP_ID_19143554,Human_RBP_ID_23094601,Human_RBP_ID_26239470 Human_Splice_Rec_1063186,Human_Splice_Rec_1063187,Human_Splice_Rec_1063216,Human_Splice_Rec_1063217,Human_Splice_Rec_1063246,Human_Splice_Rec_1063247,Human_Splice_Rec_1063272,Human_Splice_Rec_1063273,Human_Splice_Rec_1063306,Human_Splice_Rec_1063307,Human_Splice_Rec_1063346,Human_Splice_Rec_1063352,Human_Splice_Rec_1063358,Human_Splice_Rec_1063359,Human_Splice_Rec_1063368,Human_Splice_Rec_1063369,Human_Splice_Rec_1063378,Human_Splice_Rec_1063379,Human_Splice_Rec_1063398,Human_Splice_Rec_1063399,Human_Splice_Rec_1063408,Human_Splice_Rec_1063409,Human_Splice_Rec_1063414,Human_Splice_Rec_1063415 Human_miRNA_ID_2269337,Human_miRNA_ID_2269338 RMVar_hsa_circ_13382,RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_29688,RMVar_hsa_circ_21069,RMVar_hsa_circ_67341,RMVar_hsa_circ_364246,RMVar_hsa_circ_257959,RMVar_hsa_circ_299975,RMVar_hsa_circ_257958,RMVar_hsa_circ_312580,RMVar_hsa_circ_357801,RMVar_hsa_circ_257960 117056 RMVar_ID_117056 Human_SNP_ID_877693870 m1A Human chr9 - 33262827 33262827 33262827 ATTCGTCAAATGCTTTTCTTTCTCCCCAGGCAATGAGAAGCACGACCTTCATGTTACCTCCCAGC ATTCGTCAAATGCTTTTCTTTCTCCCCAGGCAGTGAGAAGCACGACCTTCATGTTACCTCCCAGC T C BAG1 Ensembl:ENSG00000107262 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:33262776..33262850 26863196 MeRIP-seq:(Medium) rs1421388081 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_92340,Human_RBP_ID_9406846 Human_Splice_Rec_1038030,Human_Splice_Rec_1038056,Human_Splice_Rec_1038068,Human_Splice_Rec_1038088,Human_Splice_Rec_1038094,Human_Splice_Rec_1038098 RMVar_hsa_circ_312814,RMVar_hsa_circ_306598 117057 RMVar_ID_117057 Human_SNP_ID_877713824 m1A Human chr9 - 128178710 128178710 128178710 GAGATGCCACCTGATGCAGTAGAAGCTGGTGGAGGTAAGTGAGCACTGGCTCCCAGCTGGTCTGG GAGATGCCACCTGATGCAGTAGAAGCTGGTGGGGGTAAGTGAGCACTGGCTCCCAGCTGGTCTGG T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128178701..128178725 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 11 caecum,large intestine Human_RBP_ID_2061056,Human_RBP_ID_5407957,Human_RBP_ID_19143955 Human_Splice_Rec_1084663,Human_Splice_Rec_1084709,Human_Splice_Rec_1084741,Human_Splice_Rec_1084773,Human_Splice_Rec_1084807,Human_Splice_Rec_1084839,Human_Splice_Rec_1084877,Human_Splice_Rec_1084909,Human_Splice_Rec_1084943,Human_Splice_Rec_1084981,Human_Splice_Rec_1085009,Human_Splice_Rec_1085079 RMVar_hsa_circ_32475,RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_81234,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_362446,RMVar_hsa_circ_259854,RMVar_hsa_circ_44120,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_259856 117058 RMVar_ID_117058 Human_SNP_ID_877714075 m1A Human chr9 - 134756809 134756809 134756809 CAGGAGGGTGGTGGGTGACCTACCTTGGGGCCAGTTTGTCCAGGCATTCCTCTGGCTCCATCACT CAGGAGGGTGGTGGGTGACCTACCTTGGGGCCCGTTTGTCCAGGCATTCCTCTGGCTCCATCACT T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:134756715..134756871;chr9:134756751..134756825 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 117059 RMVar_ID_117059 Human_SNP_ID_877716047 m1A Human chr9 + 114235642 114235642 114235642 GGTTCCAGGTGTGTCAGGAGATCCCGGATTCCAAGGAGACAAGGTAATTGCATGAGATTTTCCCC GGTTCCAGGTGTGTCAGGAGATCCCGGATTCCCAGGAGACAAGGTAATTGCATGAGATTTTCCCC A C COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:114235628..114245927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung small_cell_carcinoma 1 lung Human_RBP_ID_847778,Human_RBP_ID_962171,Human_RBP_ID_5409803,Human_RBP_ID_5482400,Human_RBP_ID_5534907,Human_RBP_ID_8239219,Human_RBP_ID_9407227,Human_RBP_ID_18173172,Human_RBP_ID_18427357,Human_RBP_ID_18472703,Human_RBP_ID_19024150,Human_RBP_ID_22748004,Human_RBP_ID_23094760,Human_RBP_ID_23120852,Human_RBP_ID_26360425 Human_Splice_Rec_1073908,Human_Splice_Rec_1073909,Human_Splice_Rec_1074036,Human_Splice_Rec_1074037 RMVar_hsa_circ_18044,RMVar_hsa_circ_92377,RMVar_hsa_circ_258936,RMVar_hsa_circ_79983,RMVar_hsa_circ_114509,RMVar_hsa_circ_258938,RMVar_hsa_circ_35925,RMVar_hsa_circ_258939,RMVar_hsa_circ_31952,RMVar_hsa_circ_65651,RMVar_hsa_circ_341924 117060 RMVar_ID_117060 Human_SNP_ID_877723460 m1A Human chr9 + 136941610 136941606 136941611 TATGTCTATGACGTGGTCCAGCGCGTCGAAGAAGGCATCGGAGCCCCGGCCCTCACCCAGCACGG TATGTCTATGACGTGGTCCAGCGCGTCGA_____GCATCGGAGCCCCGGCCCTCACCCAGCACGG AAGAAG A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136941574..136941668 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 30..34 33 LIHC 1 - 117061 RMVar_ID_117061 Human_SNP_ID_877727503 m1A Human chr9 - 134685565 134685565 134685565 TGGATGGATGGAGGATGGATGGATGGATGAATAGATGGATGGATGGATGCTGGATGGATGGATGG TGGATGGATGGAGGATGGATGGATGGATGAATGGATGGATGGATGGATGCTGGATGGATGGATGG T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:134685557..134685641 26863196 MeRIP-seq:(Medium) rs1264902450 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 117062 RMVar_ID_117062 Human_SNP_ID_877727687 m1A Human chr9 - 89311224 89311224 89311224 GAAGAGCGGGCGCAGCAGACAAAACCACGTCCAGCCCAGGCAACAACTCGCCGGAGACTAACGAC GAAGAGCGGGCGCAGCAGACAAAACCACGTCCCGCCCAGGCAACAACTCGCCGGAGACTAACGAC T G - - Other Unknown GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:89311201..89311225 26863196 MeRIP-seq:(Medium) rs1028272809 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 3 kidney 117063 RMVar_ID_117063 Human_SNP_ID_877728675 m1A Human chr9 + 4860943 4860943 4860943 TGGGATGTTTTTATATTCCAGGTGTGCTGTACATTCTTATTTTATTTTCACAATAGCTCTGTGAT TGGGATGTTTTTATATTCCAGGTGTGCTGTACGTTCTTATTTTATTTTCACAATAGCTCTGTGAT A G RCL1 Ensembl:ENSG00000120158 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs295918 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_7929526,Human_RBP_ID_8928771,Human_RBP_ID_18136603,Human_RBP_ID_21906399,Human_RBP_ID_23300268,Human_RBP_ID_24304417,Human_RBP_ID_24523781,Human_RBP_ID_26563974,Human_RBP_ID_27137167,Human_RBP_ID_27786111 Human_miRNA_ID_860133 GWAS_ID_13381,GWAS_ID_13382,GWAS_ID_13383,GWAS_ID_13384 RMVar_hsa_circ_255456 117064 RMVar_ID_117064 Human_SNP_ID_877729196 m1A Human chr9 - 21974799 21974782 21974799 CAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCCACGGCCGCGG CAGCATGGAGCCGGCGGCGGGGAGCAGCATGG_________________CTGGCCACGGCCGCGG GCCAGTCAGCCGAAGGCT G CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:21974576..21974950 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..49 33 HNSC 1 - Human_RBP_ID_92522,Human_RBP_ID_717045 117065 RMVar_ID_117065 Human_SNP_ID_877743635 m1A Human chr9 - 94846358 94846358 94846358 AATTGCCTTCTTCCAGGTCACCAGTGACCCCCACTGAACCAAATCCCACAGTCCACCCTCAGTCC AATTGCCTTCTTCCAGGTCACCAGTGACCCCCGCTGAACCAAATCCCACAGTCCACCCTCAGTCC T C lnc-FANCC-74 RNACentral:URS00008B87AD lincRNA intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:94846307..94846404 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 117066 RMVar_ID_117066 Human_SNP_ID_877746267 m1A Human chr9 + 37802492 37802492 37802492 TTGGGAAAGGGATAGAAGTATTTCAGATGGAGATGATTGGTATGTCAAAGGTCGTAGAAGGGCAG TTGGGAAAGGGATAGAAGTATTTCAGATGGAGGTGATTGGTATGTCAAAGGTCGTAGAAGGGCAG A G DCAF10 Ensembl:ENSG00000122741 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:37802441..37802547 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_5226545,Human_RBP_ID_16681320,Human_RBP_ID_24303639 117067 RMVar_ID_117067 Human_SNP_ID_877747545 m1A Human chr9 + 114288740 114288740 114288740 GTGGGTGATCGAGGAGACCGCGGGGAACCGGGAGACCCTGGGTACCCTGTAAGTATCAGAGCTCC GTGGGTGATCGAGGAGACCGCGGGGAACCGGGGGACCCTGGGTACCCTGTAAGTATCAGAGCTCC A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1687410 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_847799,Human_RBP_ID_962188,Human_RBP_ID_5123968,Human_RBP_ID_5135283,Human_RBP_ID_5409847,Human_RBP_ID_5534955,Human_RBP_ID_8239365,Human_RBP_ID_9407259,Human_RBP_ID_18173192,Human_RBP_ID_18472738,Human_RBP_ID_19024217,Human_RBP_ID_22556157,Human_RBP_ID_23094646,Human_RBP_ID_23120915,Human_RBP_ID_24555423,Human_RBP_ID_26360446 Human_Splice_Rec_1073960,Human_Splice_Rec_1073961,Human_Splice_Rec_1074088,Human_Splice_Rec_1074089 GWAS_ID_8258,GWAS_ID_8259,GWAS_ID_8260,GWAS_ID_8261,GWAS_ID_8262,GWAS_ID_8263,GWAS_ID_8264,GWAS_ID_8265,GWAS_ID_8266 RMVar_hsa_circ_79983,RMVar_hsa_circ_258939,RMVar_hsa_circ_109166,RMVar_hsa_circ_258941 117068 RMVar_ID_117068 Human_SNP_ID_877748192 m1A Human chr9 - 137615110 137615110 137615110 GGGGTCAGCTCTCAGGGGTCAGGCTGGGTTCCACGCCGCCGCAGCTCTGCTCATAAGACGGTGGG GGGGTCAGCTCTCAGGGGTCAGGCTGGGTTCCGCGCCGCCGCAGCTCTGCTCATAAGACGGTGGG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HEPG2 cell line,mRNA untreated;HTR8/Svneo,Normoxia chr9:137615061..137615152;chr9:137615061..137615162 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lymph_node follicular_lymphoma,haematopoietic_and_lymphoid_tissue follicular_lymphoma 1 haematopoietic and lymphoid tissue 117069 RMVar_ID_117069 Human_SNP_ID_877751057 m1A Human chr9 + 128907871 128907871 128907871 CCGCTCAGAGACGGGCGTGCTGGACAAGAAGGAGGGGGAGCAAGCCAAGGCGCTGTTTGAGAAGG CCGCTCAGAGACGGGCGTGCTGGACAAGAAGGTGGGGGAGCAAGCCAAGGCGCTGTTTGAGAAGG A T LRRC8A Ensembl:ENSG00000136802 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:128907726..128907925;chr9:128907726..128907967;chr9:128907726..128907950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney Human_miRNA_ID_2217740,Human_miRNA_ID_2217741 RMVar_hsa_circ_260106,RMVar_hsa_circ_105058,RMVar_hsa_circ_87431,RMVar_hsa_circ_260104,RMVar_hsa_circ_260105,RMVar_hsa_circ_272509 117070 RMVar_ID_117070 Human_SNP_ID_877780883 m1A Human chr9 - 131430062 131430060 131430063 TCTGCCTTTGAAATAGAGAAGAAAAAAAAAAAAAGAGAGAGAAAAAAAAAAAAGAGTGTCACTAC TCTGCCTTTGAAATAGAGAAGAAAAAAAAAA___GAGAGAGAAAAAAAAAAAAGAGTGTCACTAC CTTT C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:131430056..131430200 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 32..34 33 COCA 1 - 117071 RMVar_ID_117071 Human_SNP_ID_877805536 m1A Human chr9 + 134798459 134798459 134798459 GACTCCCAGGACACCCTGGACAGAGAGGCGAGACTGTGAGTATCGAGGGTGCTGGGGGACGTGGC GACTCCCAGGACACCCTGGACAGAGAGGCGAGCCTGTGAGTATCGAGGGTGCTGGGGGACGTGGC A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134798401..134798475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_Splice_Rec_1097072,Human_Splice_Rec_1097073,Human_Splice_Rec_1097202,Human_Splice_Rec_1097203 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_116543,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_100791,RMVar_hsa_circ_260733,RMVar_hsa_circ_101415,RMVar_hsa_circ_96974,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_121881,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818,RMVar_hsa_circ_266377,RMVar_hsa_circ_79651,RMVar_hsa_circ_120745,RMVar_hsa_circ_78280,RMVar_hsa_circ_80362,RMVar_hsa_circ_260752,RMVar_hsa_circ_260753,RMVar_hsa_circ_126679,RMVar_hsa_circ_260755,RMVar_hsa_circ_111594,RMVar_hsa_circ_260756,RMVar_hsa_circ_260754,RMVar_hsa_circ_15415,RMVar_hsa_circ_115455,RMVar_hsa_circ_260757,RMVar_hsa_circ_115024,RMVar_hsa_circ_260758,RMVar_hsa_circ_260759 117072 RMVar_ID_117072 Human_SNP_ID_877809294 m1A Human chr9 + 136430381 136430381 136430381 GGGCAGGAAGAGTAGCTCACAGGACAGATGTCACCCTTGTGGCGGCTTCTGTACAAGACGCGGTC GGGCAGGAAGAGTAGCTCACAGGACAGATGTCGCCCTTGTGGCGGCTTCTGTACAAGACGCGGTC A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136430285..136431829 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine 117073 RMVar_ID_117073 Human_SNP_ID_877826065 m1A Human chr9 + 33442937 33442937 33442937 AGATGCCGGCTGTGCCATTGGGGCCCGAAACAAAAAGCTGGTTGTCGGCGAAGTGCCAGATTGCA AGATGCCGGCTGTGCCATTGGGGCCCGAAACATAAAGCTGGTTGTCGGCGAAGTGCCAGATTGCA A T - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:33442856..33443050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 NACA 1 - 117074 RMVar_ID_117074 Human_SNP_ID_877849734 m1A Human chr9 + 130862977 130862977 130862977 GAAGCACAAGCTGGGCGGGGGCCAGTACGGGGAGGTGTACGAGGGCGTGTGGAAGAAATACAGCC GAAGCACAAGCTGGGCGGGGGCCAGTACGGGGTGGTGTACGAGGGCGTGTGGAAGAAATACAGCC A T ABL1 Ensembl:ENSG00000097007 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:130862867..130862988 26863196 MeRIP-seq:(Medium) rs121913449 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue blast_phase_chronic_myeloid_leukaemia,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_leukaemia,haematopoietic_and_lymphoid_tissue chronic_myeloid_leukaemia 18 haematopoietic and lymphoid tissue Human_RBP_ID_8930247,Human_RBP_ID_9315258,Human_RBP_ID_18131045,Human_RBP_ID_22733076,Human_RBP_ID_27574802 Human_Splice_Rec_1091267,Human_Splice_Rec_1091289 Human_miRNA_ID_2015881 Clinvar_Rec_692 RMVar_hsa_circ_52622,RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_296068,RMVar_hsa_circ_329890,RMVar_hsa_circ_260351,RMVar_hsa_circ_371059,RMVar_hsa_circ_286405,RMVar_hsa_circ_260355,RMVar_hsa_circ_260356,RMVar_hsa_circ_260357,RMVar_hsa_circ_260354,RMVar_hsa_circ_260359,RMVar_hsa_circ_260361,RMVar_hsa_circ_304389,RMVar_hsa_circ_347830,RMVar_hsa_circ_372061,RMVar_hsa_circ_109474,RMVar_hsa_circ_260360,RMVar_hsa_circ_260358 117075 RMVar_ID_117075 Human_SNP_ID_877855681 m1A Human chr9 + 21333335 21333335 21333335 TGAATAGTATTCACAGCTTAGAACATCATCATAATCACTTGTTCCTCTGAAGTGATTGCCACCAA TGAATAGTATTCACAGCTTAGAACATCATCATGATCACTTGTTCCTCTGAAGTGATTGCCACCAA A G - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:21333284..21333381 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung 117076 RMVar_ID_117076 Human_SNP_ID_877866213 m1A Human chr9 - 125171182 125171182 125171182 GTAAATGTTTACCTTTTATTTTCTCTTTTTATAGCGGCTATGTGACTACGTTTGTGACCTCCTCT GTAAATGTTTACCTTTTATTTTCTCTTTTTATGGCGGCTATGTGACTACGTTTGTGACCTCCTCT T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:125171176..125171200 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 appendix adenocarcinoma,large_intestine adenocarcinoma 3 appendix,large intestine Human_RBP_ID_5037075,Human_RBP_ID_7897585,Human_RBP_ID_22690215 Human_Splice_Rec_1079963,Human_Splice_Rec_1079977,Human_Splice_Rec_1079989,Human_Splice_Rec_1080001 RMVar_hsa_circ_347787 117077 RMVar_ID_117077 Human_SNP_ID_877883754 m1A Human chr9 + 97922475 97922475 97922475 GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGACTCCTCCAAGCCGCGCATGGCTACTGGTTGCT GCCGCACGGGGTCGCTGTAGGCCGAGGCCCCGGCTCCTCCAAGCCGCGCATGGCTACTGGTTGCT A G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:97922384..97922515 26863196 MeRIP-seq:(Medium) rs3183927 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,colon adenocarcinoma,COCA,large_intestine adenocarcinoma 6 head and neck,large intestine GWAS_ID_14070,GWAS_ID_14071,GWAS_ID_14072,GWAS_ID_14073,GWAS_ID_14074,GWAS_ID_14075,GWAS_ID_14076,GWAS_ID_14077,GWAS_ID_14078,GWAS_ID_14079,GWAS_ID_14080,GWAS_ID_14081,GWAS_ID_14082,GWAS_ID_14083,GWAS_ID_14084,GWAS_ID_14085,GWAS_ID_14086,GWAS_ID_14087,GWAS_ID_14088,GWAS_ID_14089,GWAS_ID_14090,GWAS_ID_14091,GWAS_ID_14092 117078 RMVar_ID_117078 Human_SNP_ID_877894830 m1A Human chr9 + 136687251 136687251 136687251 CGAGCGAGGCCACGGCGGACACCGTGAAGCACAGCGCGCAGTACAGGGCGACCTTGGCGTAGAAC CGAGCGAGGCCACGGCGGACACCGTGAAGCACTGCGCGCAGTACAGGGCGACCTTGGCGTAGAAC A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136687201..136687323 32194978 MeRIP-seq:(Medium) rs1173020252 Functional Loss SNV TCGA,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 117079 RMVar_ID_117079 Human_SNP_ID_877897444 m1A Human chr9 - 134730439 134730439 134730439 GAGGAGTTGGAGGTGTCGGCGGTGCTGGTGGGAATTTCGGCCCCAGCGCCTGGGTCTGTGGGCTG GAGGAGTTGGAGGTGTCGGCGGTGCTGGTGGGGATTTCGGCCCCAGCGCCTGGGTCTGTGGGCTG T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134730139..134730558 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 117080 RMVar_ID_117080 Human_SNP_ID_877897586 m1A Human chr9 - 123381781 123381781 123381781 TCAGCCCAACCTCTCCGCCCTCTCCATGCCCAACCTCTTTGGCCAGATGCCCATGGGCACCCACA TCAGCCCAACCTCTCCGCCCTCTCCATGCCCACCCTCTTTGGCCAGATGCCCATGGGCACCCACA T G DENND1A Ensembl:ENSG00000119522 Protein coding exon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:123381735..123381813 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_5135287,Human_RBP_ID_17323614,Human_RBP_ID_18963043 117081 RMVar_ID_117081 Human_SNP_ID_877931908 m1A Human chr9 - 32987668 32987668 32987668 GGAAACACACAGGAAGAGAAAGAGATCAGGCAACAGTGATTCTATAGAAAGGGATGCTGCTCAGG GGAAACACACAGGAAGAGAAAGAGATCAGGCAGCAGTGATTCTATAGAAAGGGATGCTGCTCAGG T C APTX Ensembl:ENSG00000137074 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:32987617..32987750 26863196 MeRIP-seq:(Medium) rs955636981 Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 10 lung Human_RBP_ID_1704733,Human_RBP_ID_7921010,Human_RBP_ID_16653271 Human_Splice_Rec_1037320,Human_Splice_Rec_1037350,Human_Splice_Rec_1037442,Human_Splice_Rec_1037454,Human_Splice_Rec_1037490,Human_Splice_Rec_1037510,Human_Splice_Rec_1037526,Human_Splice_Rec_1037592,Human_Splice_Rec_1037606,Human_Splice_Rec_1037642,Human_Splice_Rec_1037672,Human_Splice_Rec_1037766,Human_Splice_Rec_1037776,Human_Splice_Rec_1037804,Human_Splice_Rec_1037846,Human_Splice_Rec_1037882,Human_Splice_Rec_1037892 RMVar_hsa_circ_47627,RMVar_hsa_circ_256299,RMVar_hsa_circ_357381,RMVar_hsa_circ_315498,RMVar_hsa_circ_269636,RMVar_hsa_circ_362679,RMVar_hsa_circ_26015,RMVar_hsa_circ_332673,RMVar_hsa_circ_360098,RMVar_hsa_circ_3133,RMVar_hsa_circ_329730,RMVar_hsa_circ_360148 117082 RMVar_ID_117082 Human_SNP_ID_877933291 m1A Human chr9 - 122826753 122826753 122826753 GACCACCCTTGATGATAAGTTGCTGGGGGAGAAACTGCAGTACTACTATAGCAGCAGTGAGGATG GACCACCCTTGATGATAAGTTGCTGGGGGAGAGACTGCAGTACTACTATAGCAGCAGTGAGGATG T C PDCL Ensembl:ENSG00000136940 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:122826702..122828531 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_710930,Human_RBP_ID_963726,Human_RBP_ID_1057776,Human_RBP_ID_9407350,Human_RBP_ID_26361063 Human_Splice_Rec_1078164 RMVar_hsa_circ_17982 117083 RMVar_ID_117083 Human_SNP_ID_877939098 m1A Human chr9 + 127451367 127451367 127451367 TCGGATGAACCCGGATTCGGGACGACCGAAGGAAGTTGCACCTTGGCCTCCTCCGAGCCGAAAGC TCGGATGAACCCGGATTCGGGACGACCGAAGGGAGTTGCACCTTGGCCTCCTCCGAGCCGAAAGC A G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:127451301..127451400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 117084 RMVar_ID_117084 Human_SNP_ID_877940696 m1A Human chr9 - 127937369 127937369 127937369 CCCCGAGCCCTGGCACCGCCAGAGCAACTACTATATAGGCTCTAGGCACGGCGCTGGCTTCATTG CCCCGAGCCCTGGCACCGCCAGAGCAACTACTGTATAGGCTCTAGGCACGGCGCTGGCTTCATTG T C DPM2 Ensembl:ENSG00000136908 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127937340..127937440 32194978 MeRIP-seq:(Medium) rs1430409084 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_21689365 RMVar_hsa_circ_259828,RMVar_hsa_circ_373847 117085 RMVar_ID_117085 Human_SNP_ID_877954941 m1A Human chr9 + 113900620 113900620 113900620 TCCTCTCCCGCGAACCCGAGCTCCCGTCTCCTAGCACCGTCCTCTCCCGCGAACCCGAGCTCCCG TCCTCTCCCGCGAACCCGAGCTCCCGTCTCCTGGCACCGTCCTCTCCCGCGAACCCGAGCTCCCG A G ZNF618 Ensembl:ENSG00000157657 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:113900617..113900729 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary 117086 RMVar_ID_117086 Human_SNP_ID_877961861 m1A Human chr9 - 32542660 32542660 32542660 TCAGAAGAATCATAGAAAGCATCATGGGAAGAAAAGAATGAAAAGTAAACGATCCAGAAGCAGGG TCAGAAGAATCATAGAAAGCATCATGGGAAGAGAAGAATGAAAAGTAAACGATCCAGAAGCAGGG T C TOPORS Ensembl:ENSG00000197579 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:32542609..32542693 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 117087 RMVar_ID_117087 Human_SNP_ID_877972769 m1A Human chr9 + 124415407 124415407 124415407 ATCAAAAGAGAAGCCTCCAACTGGTGGAGCATACACCGACACAGCCGCCATCTTCCCAAGAAAGC ATCAAAAGAGAAGCCTCCAACTGGTGGAGCATGCACCGACACAGCCGCCATCTTCCCAAGAAAGC A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:124415260..124415425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate 117088 RMVar_ID_117088 Human_SNP_ID_877992154 m1A Human chr9 + 136496260 136496260 136496260 ACCTGTAGCTGGTGGCTGGGGGTGTTGTCCACAGGCGAGGAGTAGCTGTGCTGCGAGGGGGGCGT ACCTGTAGCTGGTGGCTGGGGGTGTTGTCCACCGGCGAGGAGTAGCTGTGCTGCGAGGGGGGCGT A C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136496209..136496333 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia 1 haematopoietic and lymphoid tissue 117089 RMVar_ID_117089 Human_SNP_ID_878009273 m1A Human chr9 + 35560374 35560374 35560374 CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGAGGAGACAGAAGAGGTGGCAGAGGCAGCCGGGG CTCAGAAGGTGGAGAAGAGGAAGAGGAAGAAGTGGAGACAGAAGAGGTGGCAGAGGCAGCCGGGG A T RUSC2 Ensembl:ENSG00000198853 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35560176..35560764 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 LGG 2 - Human_RBP_ID_15303,Human_RBP_ID_219649,Human_RBP_ID_963129,Human_RBP_ID_3974469,Human_RBP_ID_19023793,Human_RBP_ID_26361685 RMVar_hsa_circ_30644,RMVar_hsa_circ_27510,RMVar_hsa_circ_67936 117090 RMVar_ID_117090 Human_SNP_ID_878010770 m1A Human chr9 + 114169159 114169159 114169159 CACTCCTGGCTCAGCTCCCACTGGAAGCAAGAAGCCCATTGGATCGGAAGCCTCAAAGAAAGCCG CACTCCTGGCTCAGCTCCCACTGGAAGCAAGAGGCCCATTGGATCGGAAGCCTCAAAGAAAGCCG A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114169112..114211016 32194978 MeRIP-seq:(Medium) rs1308219550 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach Human_RBP_ID_5226906,Human_RBP_ID_18472687,Human_RBP_ID_19024111 RMVar_hsa_circ_50777,RMVar_hsa_circ_331270,RMVar_hsa_circ_92377,RMVar_hsa_circ_258936 117091 RMVar_ID_117091 Human_SNP_ID_878011124 m1A Human chr9 - 35714077 35714077 35714077 TACACCCAAAACCCCTTTCTTATCATAGGCTCAGGAAGCATGTGGACCTTTGGAGATGGATTCTG TACACCCAAAACCCCTTTCTTATCATAGGCTCGGGAAGCATGTGGACCTTTGGAGATGGATTCTG T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35713951..35714100 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_256022 Human_Splice_Rec_1042404 Human_miRNA_ID_1544392,Human_miRNA_ID_1597083,Human_miRNA_ID_2789115 RMVar_hsa_circ_117176,RMVar_hsa_circ_112957,RMVar_hsa_circ_114387,RMVar_hsa_circ_98470,RMVar_hsa_circ_102657,RMVar_hsa_circ_99943,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_83735,RMVar_hsa_circ_256637,RMVar_hsa_circ_256632,RMVar_hsa_circ_256634,RMVar_hsa_circ_256635,RMVar_hsa_circ_256633,RMVar_hsa_circ_256630,RMVar_hsa_circ_256631,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256654,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_123260,RMVar_hsa_circ_80499,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_88040,RMVar_hsa_circ_89487,RMVar_hsa_circ_256666,RMVar_hsa_circ_90952,RMVar_hsa_circ_94664,RMVar_hsa_circ_90899,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256679,RMVar_hsa_circ_256680,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_123605,RMVar_hsa_circ_256674,RMVar_hsa_circ_90441,RMVar_hsa_circ_256684,RMVar_hsa_circ_256685,RMVar_hsa_circ_125098,RMVar_hsa_circ_118119,RMVar_hsa_circ_256689,RMVar_hsa_circ_256690,RMVar_hsa_circ_86846,RMVar_hsa_circ_108625,RMVar_hsa_circ_120669,RMVar_hsa_circ_84308,RMVar_hsa_circ_256693,RMVar_hsa_circ_256695,RMVar_hsa_circ_256694,RMVar_hsa_circ_256692,RMVar_hsa_circ_88668,RMVar_hsa_circ_256699,RMVar_hsa_circ_102302,RMVar_hsa_circ_112542,RMVar_hsa_circ_100834,RMVar_hsa_circ_256704,RMVar_hsa_circ_84754,RMVar_hsa_circ_80829,RMVar_hsa_circ_256700,RMVar_hsa_circ_256702,RMVar_hsa_circ_256703,RMVar_hsa_circ_256701,RMVar_hsa_circ_116270,RMVar_hsa_circ_256712,RMVar_hsa_circ_256714,RMVar_hsa_circ_100663,RMVar_hsa_circ_84286,RMVar_hsa_circ_256715,RMVar_hsa_circ_256719,RMVar_hsa_circ_119193,RMVar_hsa_circ_101449,RMVar_hsa_circ_102314,RMVar_hsa_circ_103219,RMVar_hsa_circ_77736,RMVar_hsa_circ_124790,RMVar_hsa_circ_256723,RMVar_hsa_circ_256724,RMVar_hsa_circ_256722,RMVar_hsa_circ_256725,RMVar_hsa_circ_1552,RMVar_hsa_circ_85007,RMVar_hsa_circ_256726,RMVar_hsa_circ_81316,RMVar_hsa_circ_256728,RMVar_hsa_circ_256729,RMVar_hsa_circ_76800,RMVar_hsa_circ_256730,RMVar_hsa_circ_86014,RMVar_hsa_circ_86312,RMVar_hsa_circ_256731,RMVar_hsa_circ_106251,RMVar_hsa_circ_100421,RMVar_hsa_circ_256732,RMVar_hsa_circ_256733,RMVar_hsa_circ_52224,RMVar_hsa_circ_59228,RMVar_hsa_circ_95916,RMVar_hsa_circ_256734,RMVar_hsa_circ_256735 117092 RMVar_ID_117092 Human_SNP_ID_878021078 m1A Human chr9 + 69121343 69121343 69121343 TGCGTCTCCCTCCCGGGGCTCGCGCGCCCAGAACCCTCCGGTCTCAAGGAAGCAGGTGACAGCCG TGCGTCTCCCTCCCGGGGCTCGCGCGCCCAGACCCCTCCGGTCTCAAGGAAGCAGGTGACAGCCG A C TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding 5'UTR,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:69121292..69121433 26863196 MeRIP-seq:(Medium) rs1564361405 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_9408067 Human_Splice_Rec_1049825,Human_Splice_Rec_1049829,Human_Splice_Rec_1049871,Human_Splice_Rec_1049873 117093 RMVar_ID_117093 Human_SNP_ID_878024366 m1A Human chr9 - 136476479 136476479 136476479 TCAGGAGCTCTGGCGATGTTTTTCCAAGGGGGAGAGACAGAAAATGAGGAGAATCTCTCATCTGA TCAGGAGCTCTGGCGATGTTTTTCCAAGGGGGGGAGACAGAAAATGAGGAGAATCTCTCATCTGA T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:136476429..136476498 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_317622,Human_RBP_ID_18132345,Human_RBP_ID_22119113,Human_RBP_ID_22733877,Human_RBP_ID_27133487 RMVar_hsa_circ_269804,RMVar_hsa_circ_61233,RMVar_hsa_circ_65878 117094 RMVar_ID_117094 Human_SNP_ID_878025242 m1A Human chr9 - 93113033 93113033 93113033 GCGGCTGACATGTCTGTCGATGATGACAGGCGAGAAACCGAGGACGCGCCGGGTCCCTGGCAGGC GCGGCTGACATGTCTGTCGATGATGACAGGCGGGAAACCGAGGACGCGCCGGGTCCCTGGCAGGC T C - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:93112282..93113233 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 117095 RMVar_ID_117095 Human_SNP_ID_878035839 m1A Human chr9 + 91423746 91423746 91423746 GGGCCGGGCCGGGCCTCCGGGGCCGCGGCGGGAGGCGGGCGGCGGCGAGGGCGCGGCGCGGGAGG GGGCCGGGCCGGGCCTCCGGGGCCGCGGCGGGGGGCGGGCGGCGGCGAGGGCGCGGCGCGGGAGG A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:91423655..91423805 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 117096 RMVar_ID_117096 Human_SNP_ID_878052599 m1A Human chr9 - 78236328 78236328 78236328 AGTCGATCATGGCCCGAGGGCGGCCTCGGGGGATGCCCGCCGCGGAGACGCCGCCCGCGCCCACC AGTCGATCATGGCCCGAGGGCGGCCTCGGGGGGTGCCCGCCGCGGAGACGCCGCCCGCGCCCACC T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:78236129..78236400 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 13 large intestine 117097 RMVar_ID_117097 Human_SNP_ID_878087089 m1A Human chr9 - 98026196 98026196 98026196 ATTTCCTCTCTCCCTAACCCCAGACCCTATTAACCTCTTGCCAGCCTGTCCACTTCTCTAGCTCA ATTTCCTCTCTCCCTAACCCCAGACCCTATTACCCTCTTGCCAGCCTGTCCACTTCTCTAGCTCA T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:98026185..98026258 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 117098 RMVar_ID_117098 Human_SNP_ID_878099930 m1A Human chr9 + 37430911 37430911 37430911 CGGCGGGGCCTGGCACACAGCAGCGTGGCTTCAGGGAGTGTTCCCAGGGAGCCTCTGCAGGCCCA CGGCGGGGCCTGGCACACAGCAGCGTGGCTTCGGGGAGTGTTCCCAGGGAGCCTCTGCAGGCCCA A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37430908..37431059 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_13733,RMVar_hsa_circ_122450,RMVar_hsa_circ_298731,RMVar_hsa_circ_256905,RMVar_hsa_circ_256906,RMVar_hsa_circ_87063,RMVar_hsa_circ_256913,RMVar_hsa_circ_256914,RMVar_hsa_circ_329994 117099 RMVar_ID_117099 Human_SNP_ID_878104269 m1A Human chr9 - 124877228 124877228 124877228 GGATCTGCACCTGCCCAAACCATCCCTCCCCCAGTGCACACAGGTGCATCTGACCAACACCAGCC GGATCTGCACCTGCCCAAACCATCCCTCCCCCGGTGCACACAGGTGCATCTGACCAACACCAGCC T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:124877178..124877267 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 117100 RMVar_ID_117100 Human_SNP_ID_878111748 m1A Human chr9 - 21970950 21970950 21970950 TCGCACGGTACCTGCGCGCGGCTGCGGGGGGCACCAGAGGCAGTAACCATGCCCGCATAGATGCC TCGCACGGTACCTGCGCGCGGCTGCGGGGGGCGCCAGAGGCAGTAACCATGCCCGCATAGATGCC T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:21970829..21971228 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 10 liver Human_RBP_ID_717032,Human_RBP_ID_5042028,Human_RBP_ID_7916560,Human_RBP_ID_24297449,Human_RBP_ID_27135406,Human_RBP_ID_27374362,Human_RBP_ID_27545286 Human_Splice_Rec_1035551,Human_Splice_Rec_1035555,Human_Splice_Rec_1035561,Human_Splice_Rec_1035569,Human_Splice_Rec_1035575,Human_Splice_Rec_1035579,Human_Splice_Rec_1035585,Human_Splice_Rec_1035589,Human_Splice_Rec_1035593 117101 RMVar_ID_117101 Human_SNP_ID_878131601 m1A Human chr9 - 74952330 74952330 74952330 GGCCAGGAGCGTGAGGACCACGGTCTGGAGACAGGCGATCCGCCGCTGCCGCCGCCGCCCGTACT GGCCAGGAGCGTGAGGACCACGGTCTGGAGACTGGCGATCCGCCGCTGCCGCCGCCGCCCGTACT T A C9orf40 Ensembl:ENSG00000135045 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:74952242..74952400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_9338923 Human_miRNA_ID_2225240 RMVar_hsa_circ_257176,RMVar_hsa_circ_108639 117102 RMVar_ID_117102 Human_SNP_ID_878139609 m1A Human chr9 + 114587885 114587885 114587885 TCAGGGGATTCAGCAGCTGCTGCAGGCCGAGAAGCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCA TCAGGGGATTCAGCAGCTGCTGCAGGCCGAGAGGCGGGCAGCCGAGAAGGTGTCCGAGGCCCGCA A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:114587751..114587997 26863196 MeRIP-seq:(Medium) rs781231977 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_92478,Human_RBP_ID_5036349,Human_RBP_ID_8944637,Human_RBP_ID_9407276,Human_RBP_ID_16548343,Human_RBP_ID_19143761,Human_RBP_ID_26360462,Human_RBP_ID_27833311 Human_Splice_Rec_1074477 117103 RMVar_ID_117103 Human_SNP_ID_878148530 m1A Human chr9 + 100292596 100292596 100292596 GCACGATAGCCACTGGAAGCCCAGCAGGCGGCATGACACAGAACCCAAGGCCAAATGTGCCCCCC GCACGATAGCCACTGGAAGCCCAGCAGGCGGCCTGACACAGAACCCAAGGCCAAATGTGCCCCCC A C INVS Ensembl:ENSG00000119509 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:100292429..100292598 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - RMVar_hsa_circ_37468,RMVar_hsa_circ_109150,RMVar_hsa_circ_37779,RMVar_hsa_circ_258271,RMVar_hsa_circ_265159,RMVar_hsa_circ_55156,RMVar_hsa_circ_7197,RMVar_hsa_circ_47096,RMVar_hsa_circ_15547 117104 RMVar_ID_117104 Human_SNP_ID_878150730 m1A Human chr9 - 37753849 37753849 37753849 CCAGCCCCCTTAACCAGCGGACAGCGTACCTGATCCCCTCACCCCCACGCAGCGGCAGCGGCGCG CCAGCCCCCTTAACCAGCGGACAGCGTACCTGCTCCCCTCACCCCCACGCAGCGGCAGCGGCGCG T G AL138752.2 Ensembl:ENSG00000255872 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:37753836..37753907;chr9:37753827..37753904 26863196 MeRIP-seq:(Medium) rs7848132 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver 117105 RMVar_ID_117105 Human_SNP_ID_878160008 m1A Human chr9 + 127447738 127447737 127447738 TGTTTTCCTTTGTGCTTAACTCTGTGGGAAAGAAAAAAAAAATCAGTAAAAAGTTTAAAAGGATT TGTTTTCCTTTGTGCTTAACTCTGTGGGAAAG_AAAAAAAAATCAGTAAAAAGTTTAAAAGGATT GA G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:127447722..127447821 32194978 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..33 33 COCA 1 - 117106 RMVar_ID_117106 Human_SNP_ID_878169141 m1A Human chr9 + 35685297 35685297 35685297 TTACCTCTCGGCCACCTCAGCCCTCTCCTCCGAGCGCTCCAGCTCTCCTTCCAGGATCACCAGCT TTACCTCTCGGCCACCTCAGCCCTCTCCTCCGGGCGCTCCAGCTCTCCTTCCAGGATCACCAGCT A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:35685276..35685300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 6 liver 117107 RMVar_ID_117107 Human_SNP_ID_878179758 m1A Human chr9 - 91733298 91733298 91733298 CCGGACACCCAAGCCGCGTGAGCTGTGCCGCGACGAGTGCGAGGTGCTGGAGAGCGACCTGTGCC CCGGACACCCAAGCCGCGTGAGCTGTGCCGCGGCGAGTGCGAGGTGCTGGAGAGCGACCTGTGCC T C ROR2 Ensembl:ENSG00000169071 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:91733247..91733391 26863196 MeRIP-seq:(Medium) rs760726459 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_18196901 RMVar_hsa_circ_50162 117108 RMVar_ID_117108 Human_SNP_ID_878192078 m1A Human chr9 - 93268661 93268661 93268661 GGGGCCTCGGGGGCGGGGTGCTCAGCCACCGGACAGATGATGAACCACCTCTTCCCGGTGTGCAG GGGGCCTCGGGGGCGGGGTGCTCAGCCACCGGGCAGATGATGAACCACCTCTTCCCGGTGTGCAG T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:93268624..93268689;chr9:93268622..93268742 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 117109 RMVar_ID_117109 Human_SNP_ID_878202484 m1A Human chr9 + 137243543 137243543 137243543 GGAGGAGGGCGAGTTCGAGGAGGAGGCTGAGGAGGAGGTGGCCTAGAGCCTTCAGTCACTGGGGA GGAGGAGGGCGAGTTCGAGGAGGAGGCTGAGGGGGAGGTGGCCTAGAGCCTTCAGTCACTGGGGA A G TUBB4B Ensembl:ENSG00000188229 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,total RNA Untreated chr9:137243426..137243657;chr9:137243426..137243649;chr9:137243426..137243600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_91870,Human_RBP_ID_715698,Human_RBP_ID_5022473,Human_RBP_ID_5124302,Human_RBP_ID_7908284,Human_RBP_ID_8239118,Human_RBP_ID_17666442,Human_RBP_ID_22466292,Human_RBP_ID_27373764 Human_miRNA_ID_2015914 RMVar_hsa_circ_80561,RMVar_hsa_circ_102310,RMVar_hsa_circ_86963,RMVar_hsa_circ_261004,RMVar_hsa_circ_117450,RMVar_hsa_circ_261005,RMVar_hsa_circ_261006,RMVar_hsa_circ_261007 117110 RMVar_ID_117110 Human_SNP_ID_878208648 m1A Human chr9 + 98011376 98011376 98011376 TGAAGATGTAGAAGGGGATGAGGACGACGATGAAGTCAGTGAGGAGGTCAGTGCAGCTGTTTTCT TGAAGATGTAGAAGGGGATGAGGACGACGATGGAGTCAGTGAGGAGGTCAGTGCAGCTGTTTTCT A G ANP32B Ensembl:ENSG00000136938 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:98011326..98011400 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 3 caecum,large intestine Human_RBP_ID_218400,Human_RBP_ID_707142,Human_RBP_ID_797479,Human_RBP_ID_847216,Human_RBP_ID_965740,Human_RBP_ID_1708012,Human_RBP_ID_5534814,Human_RBP_ID_7880740,Human_RBP_ID_9407093,Human_RBP_ID_16520678,Human_RBP_ID_18140548,Human_RBP_ID_18414501,Human_RBP_ID_18541876,Human_RBP_ID_18545068,Human_RBP_ID_19145339,Human_RBP_ID_22118765,Human_RBP_ID_23094329,Human_RBP_ID_23117222,Human_RBP_ID_23120845,Human_RBP_ID_24275444,Human_RBP_ID_24549616,Human_RBP_ID_26360390,Human_RBP_ID_27832525 Human_Splice_Rec_1066585 RMVar_hsa_circ_86610,RMVar_hsa_circ_367280,RMVar_hsa_circ_258156 117111 RMVar_ID_117111 Human_SNP_ID_878216291 m1A Human chr9 + 83970814 83970814 83970814 ATCACCATATGAGCCACGACCCCCTGCATAGGAATAATCTGATTTAAATAATGAGCAGTAAGTTC ATCACCATATGAGCCACGACCCCCTGCATAGGCATAATCTGATTTAAATAATGAGCAGTAAGTTC A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:83970707..83970868 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain 117112 RMVar_ID_117112 Human_SNP_ID_878226712 m1A Human chr9 + 128693978 128693978 128693978 TGATGAAGAGGAGGAAGGATTAGAAGATATTGACGAAGAAGGGGATGAGGATGAAGGTGAAGAAG TGATGAAGAGGAGGAAGGATTAGAAGATATTGTCGAAGAAGGGGATGAGGATGAAGGTGAAGAAG A T SET Ensembl:ENSG00000119335 Protein coding CDS GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:128693815..128694064 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_90709,Human_RBP_ID_219040,Human_RBP_ID_255848,Human_RBP_ID_712780,Human_RBP_ID_796963,Human_RBP_ID_846952,Human_RBP_ID_965239,Human_RBP_ID_1058069,Human_RBP_ID_1702401,Human_RBP_ID_2061206,Human_RBP_ID_3190146,Human_RBP_ID_3975865,Human_RBP_ID_5011887,Human_RBP_ID_5227127,Human_RBP_ID_5637075,Human_RBP_ID_7900977,Human_RBP_ID_8275126,Human_RBP_ID_8697482,Human_RBP_ID_8925605,Human_RBP_ID_9233311,Human_RBP_ID_9407614,Human_RBP_ID_10441513,Human_RBP_ID_16586291,Human_RBP_ID_17715941,Human_RBP_ID_18140668,Human_RBP_ID_18542447,Human_RBP_ID_18904287,Human_RBP_ID_21691002,Human_RBP_ID_22118893,Human_RBP_ID_22335924,Human_RBP_ID_22517816,Human_RBP_ID_22837782,Human_RBP_ID_23094401,Human_RBP_ID_23117234,Human_RBP_ID_23120865,Human_RBP_ID_23200283,Human_RBP_ID_24287929,Human_RBP_ID_24522387,Human_RBP_ID_24549666,Human_RBP_ID_26241763,Human_RBP_ID_26360516,Human_RBP_ID_26566568,Human_RBP_ID_27131104,Human_RBP_ID_27370807,Human_RBP_ID_27542532,Human_RBP_ID_27832811 Human_Splice_Rec_1087586,Human_Splice_Rec_1087587,Human_Splice_Rec_1087600,Human_Splice_Rec_1087601,Human_Splice_Rec_1087614,Human_Splice_Rec_1087615,Human_Splice_Rec_1087628,Human_Splice_Rec_1087629,Human_Splice_Rec_1087642,Human_Splice_Rec_1087643,Human_Splice_Rec_1087660 RMVar_hsa_circ_260064,RMVar_hsa_circ_76862,RMVar_hsa_circ_112044,RMVar_hsa_circ_365387,RMVar_hsa_circ_260058,RMVar_hsa_circ_122060,RMVar_hsa_circ_260059,RMVar_hsa_circ_100662,RMVar_hsa_circ_81778,RMVar_hsa_circ_260060,RMVar_hsa_circ_102041,RMVar_hsa_circ_260061,RMVar_hsa_circ_110943,RMVar_hsa_circ_260062,RMVar_hsa_circ_260063,RMVar_hsa_circ_120725,RMVar_hsa_circ_260065,RMVar_hsa_circ_260066,RMVar_hsa_circ_109265,RMVar_hsa_circ_260068,RMVar_hsa_circ_260067,RMVar_hsa_circ_376959,RMVar_hsa_circ_378170 117113 RMVar_ID_117113 Human_SNP_ID_878228166 m1A Human chr9 - 107487649 107487649 107487649 CTGGCAGCGAGTACGGCAGCCCGTCGGTCATCAGCGTCAGCAAAGGCAGCCCTGACGGCAGCCAC CTGGCAGCGAGTACGGCAGCCCGTCGGTCATCGGCGTCAGCAAAGGCAGCCCTGACGGCAGCCAC T C KLF4 Ensembl:ENSG00000136826 Protein coding exon GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:107487598..107487746 26863196 MeRIP-seq:(Medium) rs746813034 Functional Loss SNV COSMIC 33..33 33 skin squamous_cell_carcinoma 2 skin Human_RBP_ID_27128775 117114 RMVar_ID_117114 Human_SNP_ID_878229199 m1A Human chr9 + 130884115 130884115 130884115 ACTTGTTCAGCGCCTTGATCAAGAAGAAGAAGAAGACAGCCCCAACCCCTCCCAAACGCAGCAGC ACTTGTTCAGCGCCTTGATCAAGAAGAAGAAGTAGACAGCCCCAACCCCTCCCAAACGCAGCAGC A T ABL1 Ensembl:ENSG00000097007 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130884065..130884212 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_8930263,Human_RBP_ID_9264706,Human_RBP_ID_9315265,Human_RBP_ID_22118960 Human_miRNA_ID_1236309,Human_miRNA_ID_1562356,Human_miRNA_ID_2153261,Human_miRNA_ID_2801136,Human_miRNA_ID_3009264 RMVar_hsa_circ_260352,RMVar_hsa_circ_76537,RMVar_hsa_circ_109474,RMVar_hsa_circ_260358,RMVar_hsa_circ_88938,RMVar_hsa_circ_260363,RMVar_hsa_circ_104714,RMVar_hsa_circ_260365 117115 RMVar_ID_117115 Human_SNP_ID_878238054 m1A Human chr9 - 95468998 95468998 95468998 CATGCAGTCCACTGTCCAGCTCCGCACGGAGTACGACCCCCACACGCACGTGTACTACACCACCG CATGCAGTCCACTGTCCAGCTCCGCACGGAGTGCGACCCCCACACGCACGTGTACTACACCACCG T C PTCH1 Ensembl:ENSG00000185920 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:95468869..95469076;chr9:95468948..95469050 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach RMVar_hsa_circ_38173,RMVar_hsa_circ_376435,RMVar_hsa_circ_257978,RMVar_hsa_circ_122253,RMVar_hsa_circ_301354,RMVar_hsa_circ_257977 117116 RMVar_ID_117116 Human_SNP_ID_878245759 m1A Human chr9 - 16416997 16416997 16416997 TTCATCAGTCTAAAAGTTAGAAATATCCCTTTATTTTAACTTTTATGTCGTTTCCATTTTTCATG TTCATCAGTCTAAAAGTTAGAAATATCCCTTTGTTTTAACTTTTATGTCGTTTCCATTTTTCATG T C BNC2 Ensembl:ENSG00000173068 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1999032 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,liver hepatocellular_carcinoma 2 liver Human_miRNA_ID_299278,Human_miRNA_ID_1754841 GWAS_ID_6834 117117 RMVar_ID_117117 Human_SNP_ID_878253276 m1A Human chr9 - 129632717 129632717 129632717 CCTTGGAATAGAATTGCTTCTCGTCTTCTATCACCTCGCTCGTCATGCTGTCACCAACCACGGCT CCTTGGAATAGAATTGCTTCTCGTCTTCTATCGCCTCGCTCGTCATGCTGTCACCAACCACGGCT T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:129632651..129632917 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 9 large intestine 117118 RMVar_ID_117118 Human_SNP_ID_878257372 m1A Human chr9 + 35102797 35102797 35102797 TTTCGGGGCAATCCAGAGGAGGCGCGGCGCGGAGCGCGGCCAGAAGCCAGTAGAGAGCCCTGAAG TTTCGGGGCAATCCAGAGGAGGCGCGGCGCGGCGCGCGGCCAGAAGCCAGTAGAGAGCCCTGAAG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570;GSE73941:GSM1906577,GSM1906578,GSM1906579,GSM1906580;GSE70485:GSM1972531,GSM1972532 HEK293T,ALKBH3 KO;HEK293T,Starvation treatment;HEPG2 cell line,mRNA heat shock 4h chr9:35102701..35103150;chr9:35102773..35103097;chr9:35102751..35102825 26863410,26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 117119 RMVar_ID_117119 Human_SNP_ID_878284502 m1A Human chr9 - 128166376 128166376 128166376 AGAAATACAAGGCGGCCAAGAACCCCAGCCCCACCACCCGACCTGTGAGCCGCCGGTGCGCAATC AGAAATACAAGGCGGCCAAGAACCCCAGCCCCGCCACCCGACCTGTGAGCCGCCGGTGCGCAATC T C CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128166326..128166678 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus Human_RBP_ID_961588,Human_RBP_ID_3974821,Human_RBP_ID_9339075,Human_RBP_ID_18197159,Human_RBP_ID_19025664,Human_RBP_ID_26362115 Human_Splice_Rec_1084680,Human_Splice_Rec_1084690,Human_Splice_Rec_1084694,Human_Splice_Rec_1084726,Human_Splice_Rec_1084758,Human_Splice_Rec_1084790,Human_Splice_Rec_1084824,Human_Splice_Rec_1084858,Human_Splice_Rec_1084864,Human_Splice_Rec_1084894,Human_Splice_Rec_1084926,Human_Splice_Rec_1084960,Human_Splice_Rec_1084998,Human_Splice_Rec_1085026,Human_Splice_Rec_1085042,Human_Splice_Rec_1085044 Human_miRNA_ID_1706195,Human_miRNA_ID_2777432 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 117120 RMVar_ID_117120 Human_SNP_ID_878287738 m1A Human chr9 + 87731099 87731099 87731099 ATTGTGGAATTGCCTCAGCAGCCAGCTACCCCACTGTGTGAGCTGGTGGACGGTGATGAGGAAGG ATTGTGGAATTGCCTCAGCAGCCAGCTACCCCCCTGTGTGAGCTGGTGGACGGTGATGAGGAAGG A C CTSL Ensembl:ENSG00000135047 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:87731026..87731150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_721443,Human_RBP_ID_798707,Human_RBP_ID_5033382,Human_RBP_ID_5124360,Human_RBP_ID_5154641,Human_RBP_ID_5634253,Human_RBP_ID_17666499,Human_RBP_ID_21906611,Human_RBP_ID_21995842,Human_RBP_ID_22118728,Human_RBP_ID_22466410,Human_RBP_ID_22776871,Human_RBP_ID_24311541 Human_Splice_Rec_1058774,Human_Splice_Rec_1058786,Human_Splice_Rec_1058800,Human_Splice_Rec_1058808 117121 RMVar_ID_117121 Human_SNP_ID_878288778 m1A Human chr9 - 14313820 14313820 14313820 AACTGCAAAATAGAAAACAAATCCCCAAACCCAGGCGAAAAGCAGCCAACACCGGCGGCGGCGGC AACTGCAAAATAGAAAACAAATCCCCAAACCCGGGCGAAAAGCAGCCAACACCGGCGGCGGCGGC T C NFIB Ensembl:ENSG00000147862 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:14313726..14314248 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 117122 RMVar_ID_117122 Human_SNP_ID_878295888 m1A Human chr9 - 127886771 127886771 127886771 TCTGCTCTGTCCCAGCCAGCGGCCCCGCCTCCAGCGCATGCCCTACCACTACTACGAGCCCAAGG TCTGCTCTGTCCCAGCCAGCGGCCCCGCCTCCTGCGCATGCCCTACCACTACTACGAGCCCAAGG T A ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127886721..127886809 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_963815,Human_RBP_ID_19025644,Human_RBP_ID_19143909 Human_Splice_Rec_1083812,Human_Splice_Rec_1083838,Human_Splice_Rec_1083860,Human_Splice_Rec_1083900,Human_Splice_Rec_1083940,Human_Splice_Rec_1083950,Human_Splice_Rec_1083962,Human_Splice_Rec_1083972,Human_Splice_Rec_1083982,Human_Splice_Rec_1083994,Human_Splice_Rec_1084004,Human_Splice_Rec_1084016,Human_Splice_Rec_1084024 117123 RMVar_ID_117123 Human_SNP_ID_878296679 m1A Human chr9 - 131473576 131473576 131473576 GGTCACTTTTCTTTCTTGGAGTGGGGGCACACAGTTCTGATCCTCAGAGCGACAGCCTGTCCCAT GGTCACTTTTCTTTCTTGGAGTGGGGGCACACGGTTCTGATCCTCAGAGCGACAGCCTGTCCCAT T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131473511..131473640 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - 117124 RMVar_ID_117124 Human_SNP_ID_878306534 m1A Human chr9 - 34017157 34017157 34017157 ATTTTCTATTTTGTACATACATTATTTTGTATATACTGTATATGATGACTTCAGTGAGCAGTGAC ATTTTCTATTTTGTACATACATTATTTTGTATGTACTGTATATGATGACTTCAGTGAGCAGTGAC T C UBAP2 Ensembl:ENSG00000137073 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34017106..34017182 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_717938,Human_RBP_ID_5482460,Human_RBP_ID_21906385,Human_RBP_ID_26239271 Human_Splice_Rec_1038910,Human_Splice_Rec_1038966,Human_Splice_Rec_1039120,Human_Splice_Rec_1039156,Human_Splice_Rec_1039160 Human_miRNA_ID_2067234 RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_305118,RMVar_hsa_circ_87464,RMVar_hsa_circ_362765,RMVar_hsa_circ_256449,RMVar_hsa_circ_283254,RMVar_hsa_circ_256471,RMVar_hsa_circ_256481,RMVar_hsa_circ_275675,RMVar_hsa_circ_80358,RMVar_hsa_circ_256480,RMVar_hsa_circ_323107,RMVar_hsa_circ_121180,RMVar_hsa_circ_256482,RMVar_hsa_circ_279801,RMVar_hsa_circ_256483,RMVar_hsa_circ_337365,RMVar_hsa_circ_273673,RMVar_hsa_circ_256489,RMVar_hsa_circ_256490,RMVar_hsa_circ_279590,RMVar_hsa_circ_256492,RMVar_hsa_circ_256494,RMVar_hsa_circ_256493,RMVar_hsa_circ_291348,RMVar_hsa_circ_326979 117125 RMVar_ID_117125 Human_SNP_ID_878311674 m1A Human chr9 + 73159389 73159389 73159389 TCTAACTAAGCGAAACAATGCACAGCGTCAACAGATCAAAGCAGCATATCTCCAGGAAACAGGAA TCTAACTAAGCGAAACAATGCACAGCGTCAACTGATCAAAGCAGCATATCTCCAGGAAACAGGAA A T ANXA1 Ensembl:ENSG00000135046 Protein coding exon GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:73158526..73159446 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_91002,Human_RBP_ID_17322868,Human_RBP_ID_22466104 Human_Splice_Rec_1052856,Human_Splice_Rec_1052864,Human_Splice_Rec_1052865,Human_Splice_Rec_1052878,Human_Splice_Rec_1052879,Human_Splice_Rec_1052904,Human_Splice_Rec_1052905,Human_Splice_Rec_1052910,Human_Splice_Rec_1052911 Human_miRNA_ID_1984614 RMVar_hsa_circ_58215,RMVar_hsa_circ_115712,RMVar_hsa_circ_119809,RMVar_hsa_circ_257161,RMVar_hsa_circ_257162,RMVar_hsa_circ_27860,RMVar_hsa_circ_353156 117126 RMVar_ID_117126 Human_SNP_ID_878313550 m1A Human chr9 - 19380065 19380063 19380066 CTGGCTTTAGGTGGAGAAGGGTCTCAAGTAGGAGAAGGCTCGCCTTTCTGGGGCATGGAGCTTTT CTGGCTTTAGGTGGAGAAGGGTCTCAAGTAG___AAGGCTCGCCTTTCTGGGGCATGGAGCTTTT TCTC T RPS6 Ensembl:ENSG00000137154 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:19380056..19380250 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 READ 1 - Human_RBP_ID_5408233,Human_RBP_ID_16634484,Human_RBP_ID_17176387 RMVar_hsa_circ_13482,RMVar_hsa_circ_120519,RMVar_hsa_circ_256003 117127 RMVar_ID_117127 Human_SNP_ID_878315289 m1A Human chr9 - 92077529 92077529 92077529 AAGTGGGGGAGAGTACTTGCGACTTCAGGAGGAGGCAGAGGAGCTAGGCTGGTCGTCTGATGGGC AAGTGGGGGAGAGTACTTGCGACTTCAGGAGGTGGCAGAGGAGCTAGGCTGGTCGTCTGATGGGC T A SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:92077387..92077657 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_846256,Human_RBP_ID_7945660 RMVar_hsa_circ_102678,RMVar_hsa_circ_106687,RMVar_hsa_circ_104282,RMVar_hsa_circ_257750,RMVar_hsa_circ_257751,RMVar_hsa_circ_306309,RMVar_hsa_circ_257753,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_257758,RMVar_hsa_circ_328408,RMVar_hsa_circ_90440,RMVar_hsa_circ_257759,RMVar_hsa_circ_322947 117128 RMVar_ID_117128 Human_SNP_ID_878325231 m1A Human chr9 - 109119567 109119567 109119567 CCGCCACTGGCTGCAGCGCCTGCACCGCGCGCACACGCCCATCGTCCTGGCCGCGCTGCTCCTGC CCGCCACTGGCTGCAGCGCCTGCACCGCGCGCCCACGCCCATCGTCCTGGCCGCGCTGCTCCTGC T G TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:109119496..109119691 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_255793,Human_RBP_ID_5036965,Human_RBP_ID_17437134,Human_RBP_ID_27540971 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584 117129 RMVar_ID_117129 Human_SNP_ID_878350819 m1A Human chr9 + 14889 14889 14889 GCGGCAAAGGAGGGATGGAGTCTGACACGCGGACAAAGGCTCCTCCGGGCCCCTCACCAGCCCCA GCGGCAAAGGAGGGATGGAGTCTGACACGCGGGCAAAGGCTCCTCCGGGCCCCTCACCAGCCCCA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:14816..14916 32194978 MeRIP-seq:(Medium) rs71509924 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,COCA,head_neck squamous_cell_carcinoma,liver neoplasm 21 liver,head and neck,prostate 117130 RMVar_ID_117130 Human_SNP_ID_878351777 m1A Human chr9 - 93259041 93259041 93259041 CTCGGCAAGATCACGGCTGGAGAGAAATACTGAGGTGGTGGCACGGGAGGCACAGTCGCGGTCGG CTCGGCAAGATCACGGCTGGAGAGAAATACTGCGGTGGTGGCACGGGAGGCACAGTCGCGGTCGG T G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:93258991..93259197 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 117131 RMVar_ID_117131 Human_SNP_ID_878356821 m1A Human chr9 + 17273733 17273733 17273733 TTTGATTATTGATATAAGCACTCTAATTTTAGACCTTTGAAGACAATTTAATTGAAGCAAGGAAA TTTGATTATTGATATAAGCACTCTAATTTTAGGCCTTTGAAGACAATTTAATTGAAGCAAGGAAA A G CNTLN Ensembl:ENSG00000044459 Protein coding CDS GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs3808795 Functional Loss SNV ICGC,COSMIC 33..33 33 THCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_Splice_Rec_1034128,Human_Splice_Rec_1034138 GWAS_ID_6835,GWAS_ID_6836,GWAS_ID_6837,GWAS_ID_6838,GWAS_ID_6839,GWAS_ID_6840,GWAS_ID_6841,GWAS_ID_6842,GWAS_ID_6843,GWAS_ID_6844,GWAS_ID_6845,GWAS_ID_6846,GWAS_ID_6847,GWAS_ID_6848,GWAS_ID_6849,GWAS_ID_6850,GWAS_ID_6851,GWAS_ID_6852 RMVar_hsa_circ_24596,RMVar_hsa_circ_70856,RMVar_hsa_circ_65330,RMVar_hsa_circ_60085,RMVar_hsa_circ_353376,RMVar_hsa_circ_355703,RMVar_hsa_circ_304454,RMVar_hsa_circ_66215,RMVar_hsa_circ_367848,RMVar_hsa_circ_358940,RMVar_hsa_circ_301881,RMVar_hsa_circ_326214,RMVar_hsa_circ_364095,RMVar_hsa_circ_326285,RMVar_hsa_circ_54887,RMVar_hsa_circ_255862 117132 RMVar_ID_117132 Human_SNP_ID_878359448 m1A Human chr9 - 14921829 14921829 14921829 TATTGGAAGTGGTTGCAATCTGGATTCAGCCCAATTCCGTTACCTGATGGGGGAAAGGCTGGGAG TATTGGAAGTGGTTGCAATCTGGATTCAGCCCGATTCCGTTACCTGATGGGGGAAAGGCTGGGAG T C CLCN3P1,LDHAP4 Ensembl:ENSG00000232000,Ensembl:ENSG00000214110 Pseudogene,Pseudogene exon,exon GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs555929180 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_964532,Human_RBP_ID_1708134,Human_RBP_ID_3911117,Human_RBP_ID_5229613,Human_RBP_ID_9264791,Human_RBP_ID_10440581,Human_RBP_ID_17322827,Human_RBP_ID_17579765,Human_RBP_ID_17674183,Human_RBP_ID_18140442,Human_RBP_ID_18427719,Human_RBP_ID_18508051,Human_RBP_ID_22466033,Human_RBP_ID_22530896,Human_RBP_ID_22776414,Human_RBP_ID_24392183 Human_miRNA_ID_1835091 117133 RMVar_ID_117133 Human_SNP_ID_878366464 m1A Human chr9 + 93587521 93587521 93587521 ATGGAGGAGCCCCGGGTGAGGGATGATGGAGGAGTCCCAGATAGTGGATGGAGGAGCCCCGGGTG ATGGAGGAGCCCCGGGTGAGGGATGATGGAGGCGTCCCAGATAGTGGATGGAGGAGCCCCGGGTG A C PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:93587084..93587627;chr9:93587042..93587620;chr9:93587116..93587609 26863196 MeRIP-seq:(Medium) rs148880827 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate Human_RBP_ID_9442285 117134 RMVar_ID_117134 Human_SNP_ID_878383361 m1A Human chr9 + 134728734 134728734 134728734 TTACTACGAATACCCCTACTACGAAGACCCCGAAGACCTAGGGAAGGAGCCCACCCCCAGCAAGA TTACTACGAATACCCCTACTACGAAGACCCCGCAGACCTAGGGAAGGAGCCCACCCCCAGCAAGA A C COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:134728622..134728961 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_Splice_Rec_1097010,Human_Splice_Rec_1097011,Human_Splice_Rec_1097140,Human_Splice_Rec_1097141 Human_miRNA_ID_1706354 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_313301,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742 117135 RMVar_ID_117135 Human_SNP_ID_878405213 m1A Human chr9 - 14710 14710 14710 CAGGACAAGCTGCTCAGACCTGCTTCCCTGGGAGGGGGTGACGGAACCAGCAGTGTGTGGAGACC CAGGACAAGCTGCTCAGACCTGCTTCCCTGGGTGGGGGTGACGGAACCAGCAGTGTGTGGAGACC T A WASHC1 Ensembl:ENSG00000181404 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1404595755 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LICA,liver neoplasm,liver hepatocellular_carcinoma 9 liver,prostate Human_RBP_ID_18172953 117136 RMVar_ID_117136 Human_SNP_ID_878411417 m1A Human chr9 + 21974759 21974759 21974759 GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGCCCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:21974676..21975075 26863196 MeRIP-seq:(Medium) rs766772030 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Clinvar_Rec_185 117137 RMVar_ID_117137 Human_SNP_ID_878411448 m1A Human chr9 + 21974759 21974759 21974759 GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGTCCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:21974676..21975075 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary clear_cell_carcinoma 7 ovary 117138 RMVar_ID_117138 Human_SNP_ID_878427021 m1A Human chr9 + 114597619 114597619 114597619 CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCAGGAGAAGATGACCATCCTCCAGACATACTTCC CAGTTGCAGCACTGAAGTGGAGAAGGAGACCCTGGAGAAGATGACCATCCTCCAGACATACTTCC A T ATP6V1G1 Ensembl:ENSG00000136888 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:114597551..114597632 26863196 MeRIP-seq:(Medium) rs145627791 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_2059703,Human_RBP_ID_7890884,Human_RBP_ID_9407278,Human_RBP_ID_18541899,Human_RBP_ID_19143762,Human_RBP_ID_22118823,Human_RBP_ID_22467003,Human_RBP_ID_23117230,Human_RBP_ID_26833429,Human_RBP_ID_27833312 Human_Splice_Rec_1074480 117139 RMVar_ID_117139 Human_SNP_ID_878432514 m1A Human chr9 - 89423881 89423881 89423881 AGTAGTGGAGGGAGAGGAGGTGCTGAGGGAATAGCTGAGGGAGGGGAGGTGCTGAGGGAGTGGAG AGTAGTGGAGGGAGAGGAGGTGCTGAGGGAATCGCTGAGGGAGGGGAGGTGCTGAGGGAGTGGAG T G SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:89423856..89423928 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 7 ovary RMVar_hsa_circ_125831,RMVar_hsa_circ_257716 117140 RMVar_ID_117140 Human_SNP_ID_878436285 m1A Human chr9 - 26887512 26887512 26887512 GTTTAATGGTTCTTTATTCTTTTAACTTTAGGAAACTAAATATATTTTGCCAACTTTGGAAAAAG GTTTAATGGTTCTTTATTCTTTTAACTTTAGGGAACTAAATATATTTTGCCAACTTTGGAAAAAG T C CAAP1 Ensembl:ENSG00000120159 Protein coding CDS GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:26887465..26892310 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_26242866 Human_Splice_Rec_1036236,Human_Splice_Rec_1036246,Human_Splice_Rec_1036260,Human_Splice_Rec_1036272,Human_Splice_Rec_1036282 RMVar_hsa_circ_281044,RMVar_hsa_circ_63291,RMVar_hsa_circ_256223,RMVar_hsa_circ_280343,RMVar_hsa_circ_256224 117141 RMVar_ID_117141 Human_SNP_ID_878462326 m1A Human chr9 - 127542015 127542015 127542015 GGCAGGACTTCAGTGGCTGCGGCGGGCACAGGACGGGAGTGGCCTGGCTGGGGGGCAGTGACTAG GGCAGGACTTCAGTGGCTGCGGCGGGCACAGGGCGGGAGTGGCCTGGCTGGGGGGCAGTGACTAG T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:127542010..127542137 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_8223388 RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 117142 RMVar_ID_117142 Human_SNP_ID_878468011 m1A Human chr9 - 21974799 21974799 21974799 CAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCCACGGCCGCGG CAGCATGGAGCCGGCGGCGGGGAGCAGCATGGTGCCTTCGGCTGACTGGCTGGCCACGGCCGCGG T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:21974576..21974950 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_92522,Human_RBP_ID_717045 117143 RMVar_ID_117143 Human_SNP_ID_878501440 m1A Human chr9 + 133052111 133052111 133052111 TCTGGTCCCGAAATGCTGTCAAGGCCAACATCAGCGTCCACCCAGACAAGCTCAAGGTCTTGCTT TCTGGTCCCGAAATGCTGTCAAGGCCAACATCGGCGTCCACCCAGACAAGCTCAAGGTCTTGCTT A G GTF3C5 Ensembl:ENSG00000148308 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133052021..133052196 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach Human_RBP_ID_91465,Human_RBP_ID_18453263,Human_RBP_ID_19025947,Human_RBP_ID_26833710 Human_Splice_Rec_1094699,Human_Splice_Rec_1094717,Human_Splice_Rec_1094741,Human_Splice_Rec_1094777 RMVar_hsa_circ_26734,RMVar_hsa_circ_90557,RMVar_hsa_circ_101759,RMVar_hsa_circ_127311,RMVar_hsa_circ_111001,RMVar_hsa_circ_91387,RMVar_hsa_circ_260599,RMVar_hsa_circ_260601,RMVar_hsa_circ_260603,RMVar_hsa_circ_76424,RMVar_hsa_circ_260602,RMVar_hsa_circ_260600,RMVar_hsa_circ_260598,RMVar_hsa_circ_111204,RMVar_hsa_circ_260605,RMVar_hsa_circ_108176,RMVar_hsa_circ_374999,RMVar_hsa_circ_260604,RMVar_hsa_circ_352608,RMVar_hsa_circ_82287,RMVar_hsa_circ_260607,RMVar_hsa_circ_260608 117144 RMVar_ID_117144 Human_SNP_ID_878526947 m1A Human chr9 - 128625907 128625907 128625907 GCGGGCGGCTGAGTTGGCCAGAAGCTGGCTCCACCTCTTCATGAGGGAGGCGTGCCGGGCCTCGA GCGGGCGGCTGAGTTGGCCAGAAGCTGGCTCCCCCTCTTCATGAGGGAGGCGTGCCGGGCCTCGA T G - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:128625858..128626000 26863196 MeRIP-seq:(Medium) rs766038302 Functional Loss SNV COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma 5 kidney 117145 RMVar_ID_117145 Human_SNP_ID_878527103 m1A Human chr9 - 136942138 136942138 136942138 GACCAAGGTGGCCGAGCTGCTGGCCCAGGGCCACACCAAGCCACCCGAGCGCAGTGCCACAGGCG GACCAAGGTGGCCGAGCTGCTGGCCCAGGGCCGCACCAAGCCACCCGAGCGCAGTGCCACAGGCG T C FBXW5 Ensembl:ENSG00000159069 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136942026..136942925 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver neoplasm 1 liver Human_Splice_Rec_1101165,Human_Splice_Rec_1101193,Human_Splice_Rec_1101205 RMVar_hsa_circ_81707,RMVar_hsa_circ_76472,RMVar_hsa_circ_100040,RMVar_hsa_circ_260946,RMVar_hsa_circ_260947,RMVar_hsa_circ_260948 117146 RMVar_ID_117146 Human_SNP_ID_878531303 m1A Human chr9 - 127523777 127523777 127523777 GTGCCCCACACAGTTCCCGCTCATCCTCTGGCATCCTTATGCGCGTCACTACTACTTCTGCATGA GTGCCCCACACAGTTCCCGCTCATCCTCTGGCGTCCTTATGCGCGTCACTACTACTTCTGCATGA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127523726..127523850 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_1057994,Human_RBP_ID_18130039,Human_RBP_ID_23316501,Human_RBP_ID_27542212 Human_Splice_Rec_1082272,Human_Splice_Rec_1082273,Human_Splice_Rec_1082302,Human_Splice_Rec_1082303 RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_259765,RMVar_hsa_circ_122231,RMVar_hsa_circ_7962,RMVar_hsa_circ_122936,RMVar_hsa_circ_98775,RMVar_hsa_circ_259768,RMVar_hsa_circ_259769,RMVar_hsa_circ_346970,RMVar_hsa_circ_91870,RMVar_hsa_circ_48174,RMVar_hsa_circ_259771,RMVar_hsa_circ_259772,RMVar_hsa_circ_357415,RMVar_hsa_circ_43685,RMVar_hsa_circ_343610,RMVar_hsa_circ_259773,RMVar_hsa_circ_259774,RMVar_hsa_circ_259775,RMVar_hsa_circ_275532,RMVar_hsa_circ_317016,RMVar_hsa_circ_259776 117147 RMVar_ID_117147 Human_SNP_ID_878541039 m1A Human chr9 - 21802783 21802783 21802783 GGCGAACCGCTGCGGCTGGGAGGGCTCATCTCACCTTCACGGCGGTGGTGGTGGTGCCAGAGGCC GGCGAACCGCTGCGGCTGGGAGGGCTCATCTCGCCTTCACGGCGGTGGTGGTGGTGCCAGAGGCC T C - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:21802770..21802884 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 117148 RMVar_ID_117148 Human_SNP_ID_878541458 m1A Human chr9 + 137329716 137329716 137329716 GGGTCACACGGGACTACACGGGACTACACGGGACTACACGGGACTACACGGGGTCACACGGGACT GGGTCACACGGGACTACACGGGACTACACGGGGCTACACGGGACTACACGGGGTCACACGGGACT A G - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:137329313..137329809 26863196 MeRIP-seq:(Medium) rs111207789 Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 1 pancreas 117149 RMVar_ID_117149 Human_SNP_ID_878549709 m1A Human chr9 + 129340234 129340234 129340234 GTATGTGAGATGTGTGAGTTGGTGTGTATGCGAGTTGATGTGAGTTGTGTATGTGTGAGTTGGTG GTATGTGAGATGTGTGAGTTGGTGTGTATGCGTGTTGATGTGAGTTGTGTATGTGTGAGTTGGTG A T LINC01503 Ensembl:ENSG00000233901 lincRNA intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:129339532..129340982 26863196 MeRIP-seq:(Medium) rs879897451 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 117150 RMVar_ID_117150 Human_SNP_ID_878597341 m1A Human chr9 - 134796420 134796420 134796420 CTTGGAGACACCCCCGAAGGCTCCAGCTGCTTACCCGTTCACCAGGAGGGCCAGCTGGGCCGTCA CTTGGAGACACCCCCGAAGGCTCCAGCTGCTTGCCCGTTCACCAGGAGGGCCAGCTGGGCCGTCA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134796351..134796425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine 117151 RMVar_ID_117151 Human_SNP_ID_878603867 m1A Human chr9 - 128179348 128179348 128179348 AGTTACAGGTGAAGGCCCAGCCGCAGGCCCGGATGACAGTACCGAAACAGACACAGACACCAGAC AGTTACAGGTGAAGGCCCAGCCGCAGGCCCGGTTGACAGTACCGAAACAGACACAGACACCAGAC T A CIZ1 Ensembl:ENSG00000148337 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128179303..128180453 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 11 stomach Human_RBP_ID_3974828,Human_RBP_ID_5124024,Human_RBP_ID_9407458,Human_RBP_ID_17437225,Human_RBP_ID_24549655,Human_RBP_ID_26361139,Human_RBP_ID_27833457 Human_Splice_Rec_1084660,Human_Splice_Rec_1084706,Human_Splice_Rec_1084740,Human_Splice_Rec_1084770,Human_Splice_Rec_1084804,Human_Splice_Rec_1084838,Human_Splice_Rec_1084876,Human_Splice_Rec_1084906,Human_Splice_Rec_1084940,Human_Splice_Rec_1084980,Human_Splice_Rec_1085008,Human_Splice_Rec_1085058,Human_Splice_Rec_1085076,Human_Splice_Rec_1085090,Human_Splice_Rec_1085100,Human_Splice_Rec_1085112,Human_Splice_Rec_1085120 RMVar_hsa_circ_32475,RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_81234,RMVar_hsa_circ_7211,RMVar_hsa_circ_98321,RMVar_hsa_circ_301785,RMVar_hsa_circ_259852,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_362446,RMVar_hsa_circ_259854,RMVar_hsa_circ_44120,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_73909,RMVar_hsa_circ_259856,RMVar_hsa_circ_369642,RMVar_hsa_circ_259857 117152 RMVar_ID_117152 Human_SNP_ID_878619469 m1A Human chr9 + 38395804 38395804 38395804 GCTGCTTAGCCTCCAGGGCAGGACCGCCCGCTACTCCTCGGCAGCAGCCCTCCCAAGCCCCATTC GCTGCTTAGCCTCCAGGGCAGGACCGCCCGCTGCTCCTCGGCAGCAGCCCTCCCAAGCCCCATTC A G ALDH1B1 Ensembl:ENSG00000137124 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:38395753..38395847 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_797546,Human_RBP_ID_5036181,Human_RBP_ID_22466386,Human_RBP_ID_24555550 Human_Splice_Rec_1045050,Human_Splice_Rec_1045054 Human_miRNA_ID_2088852,Human_miRNA_ID_2089729 RMVar_hsa_circ_79529,RMVar_hsa_circ_88124,RMVar_hsa_circ_256964,RMVar_hsa_circ_256965 117153 RMVar_ID_117153 Human_SNP_ID_878631985 m1A Human chr9 - 128952816 128952816 128952816 ACCTGGGAGGTTTGTAGTAAGAAAGCCCCTCTAACAATCGCCGCCAATGTTTATTCAGTTCTGCC ACCTGGGAGGTTTGTAGTAAGAAAGCCCCTCTGACAATCGCCGCCAATGTTTATTCAGTTCTGCC T C RF00017-4497 RNACentral:URS0000961FEC SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128952684..128952850 26863196 MeRIP-seq:(Medium) rs547983716 Functional Loss SNV ICGC 33..33 33 MALY 1 - 117154 RMVar_ID_117154 Human_SNP_ID_878633390 m1A Human chr9 + 4662394 4662394 4662394 GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGAGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT GGCCGCCAGCTGCGATGCCAAGTCCCCGGAGGGGCATGGAGGGACGGCCGCTGGGCGTCTCCGCT A G PLPP6 Ensembl:ENSG00000205808 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:4662345..4662664 26863196 MeRIP-seq:(Medium) rs34250374 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_RBP_ID_5035617 117155 RMVar_ID_117155 Human_SNP_ID_878639029 m1A Human chr9 - 136515624 136515624 136515624 ACGGCTCCTGCAAGGACGGCGTCGCCACCTTCACCTGCCTCTGCCGCCCAGGCTACACGGGCCAC ACGGCTCCTGCAAGGACGGCGTCGCCACCTTCCCCTGCCTCTGCCGCCCAGGCTACACGGGCCAC T G NOTCH1 Ensembl:ENSG00000148400 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:136515516..136515700 26863196 MeRIP-seq:(Medium) rs747384159 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,haematopoietic_and_lymphoid_tissue acute_lymphoblastic_T_cell_leukaemia,head_neck squamous_cell_carcinoma 6 head and neck,haematopoietic and lymphoid tissue Human_Splice_Rec_1099970 Human_miRNA_ID_2272596 RMVar_hsa_circ_106844,RMVar_hsa_circ_260876,RMVar_hsa_circ_108177,RMVar_hsa_circ_260878,RMVar_hsa_circ_260882,RMVar_hsa_circ_97625,RMVar_hsa_circ_54681,RMVar_hsa_circ_291480,RMVar_hsa_circ_260884 117156 RMVar_ID_117156 Human_SNP_ID_878645252 m1A Human chr9 - 128258158 128258158 128258158 TTTCAACTCAGCTGTAGCCAGTGCCGAGGAGGAGCAGGCAAGGCTACGTGGGCAGCTGAAGGAGC TTTCAACTCAGCTGTAGCCAGTGCCGAGGAGGGGCAGGCAAGGCTACGTGGGCAGCTGAAGGAGC T C GOLGA2 Ensembl:ENSG00000167110 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:128257976..128258268 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus Human_RBP_ID_256265,Human_RBP_ID_965538,Human_RBP_ID_3974862,Human_RBP_ID_5124433,Human_RBP_ID_5154482,Human_RBP_ID_5408727,Human_RBP_ID_9408578,Human_RBP_ID_18140972,Human_RBP_ID_18173605,Human_RBP_ID_18414534,Human_RBP_ID_19024369,Human_RBP_ID_26361164,Human_RBP_ID_27832764 Human_Splice_Rec_1085694,Human_Splice_Rec_1085742,Human_Splice_Rec_1085754,Human_Splice_Rec_1085772 RMVar_hsa_circ_93438,RMVar_hsa_circ_119177,RMVar_hsa_circ_123417,RMVar_hsa_circ_103207,RMVar_hsa_circ_259871,RMVar_hsa_circ_259873,RMVar_hsa_circ_88892,RMVar_hsa_circ_259874,RMVar_hsa_circ_259872,RMVar_hsa_circ_259870,RMVar_hsa_circ_268691 117157 RMVar_ID_117157 Human_SNP_ID_878646338 m1A Human chr9 + 114304615 114304615 114304615 CATACCCTGTCTTTTCCTTGCCCAGCAACAAGATGATCTTGGGGCAGCTTTCCAGACGTGGATGG CATACCCTGTCTTTTCCTTGCCCAGCAACAAGGTGATCTTGGGGCAGCTTTCCAGACGTGGATGG A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114301528..114306220 32194978 MeRIP-seq:(Medium) rs537785868 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 mouth squamous_cell_carcinoma,UCEC,endometrium endometrioid_carcinoma 4 uterus,head and neck Human_RBP_ID_5535456,Human_RBP_ID_18173209 Human_Splice_Rec_1073988,Human_Splice_Rec_1073989,Human_Splice_Rec_1074116,Human_Splice_Rec_1074117 RMVar_hsa_circ_79983,RMVar_hsa_circ_258939,RMVar_hsa_circ_109166,RMVar_hsa_circ_258941,RMVar_hsa_circ_258942,RMVar_hsa_circ_121039 117158 RMVar_ID_117158 Human_SNP_ID_878647173 m1A Human chr9 - 136358126 136358126 136358126 GGCCCCCGGCGAGGTCCACCCGCTGCTCGTCCATGCGCTTAGCCTGCACCCTCTGAATGAGGCTG GGCCCCCGGCGAGGTCCACCCGCTGCTCGTCCGTGCGCTTAGCCTGCACCCTCTGAATGAGGCTG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136358077..136358269 26863196 MeRIP-seq:(Medium) rs782545530 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 10 brain 117159 RMVar_ID_117159 Human_SNP_ID_878653250 m1A Human chr9 + 134753902 134753902 134753902 TTTGAAGGGCGAGCCGGGAGACGTGGGGCCTCAGGTATGTGGGATCCTTGCCTTCGCTGTCTGGT TTTGAAGGGCGAGCCGGGAGACGTGGGGCCTCGGGTATGTGGGATCCTTGCCTTCGCTGTCTGGT A G COL5A1 Ensembl:ENSG00000130635 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134753851..134753925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_1097028,Human_Splice_Rec_1097029,Human_Splice_Rec_1097158,Human_Splice_Rec_1097159 RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_12157,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260742,RMVar_hsa_circ_87513,RMVar_hsa_circ_123293,RMVar_hsa_circ_43821,RMVar_hsa_circ_121881,RMVar_hsa_circ_16104,RMVar_hsa_circ_260747,RMVar_hsa_circ_260748,RMVar_hsa_circ_268922,RMVar_hsa_circ_260749,RMVar_hsa_circ_266818 117160 RMVar_ID_117160 Human_SNP_ID_878654509 m1A Human chr9 - 21971205 21971205 21971205 GGCTCTGACCATTCTGTTCTCTCTGGCAGGTCATGATGATGGGCAGCGCCCGAGTGGCGGAGCTG GGCTCTGACCATTCTGTTCTCTCTGGCAGGTCTTGATGATGGGCAGCGCCCGAGTGGCGGAGCTG T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21970863..21971278 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 10 lung Human_RBP_ID_5024659,Human_RBP_ID_9235428,Human_RBP_ID_18134013,Human_RBP_ID_24523183 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1275357 117161 RMVar_ID_117161 Human_SNP_ID_878654513 m1A Human chr9 - 21971205 21971205 21971205 GGCTCTGACCATTCTGTTCTCTCTGGCAGGTCATGATGATGGGCAGCGCCCGAGTGGCGGAGCTG GGCTCTGACCATTCTGTTCTCTCTGGCAGGTCGTGATGATGGGCAGCGCCCGAGTGGCGGAGCTG T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:21970863..21971278 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 brain astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 10 brain Human_RBP_ID_5024659,Human_RBP_ID_9235428,Human_RBP_ID_18134013,Human_RBP_ID_24523183 Human_Splice_Rec_1035550,Human_Splice_Rec_1035554,Human_Splice_Rec_1035558,Human_Splice_Rec_1035564,Human_Splice_Rec_1035568,Human_Splice_Rec_1035574,Human_Splice_Rec_1035578,Human_Splice_Rec_1035584,Human_Splice_Rec_1035588,Human_Splice_Rec_1035596 Human_miRNA_ID_1275357 117162 RMVar_ID_117162 Human_SNP_ID_878659637 m1A Human chr9 - 87727666 87727666 87727666 CACTTGGTCCACTGTGCCTCTAAACTGTGATCAAATGTTAGAGTAGCTGAGGCAATTCCCAGGCA CACTTGGTCCACTGTGCCTCTAAACTGTGATCCAATGTTAGAGTAGCTGAGGCAATTCCCAGGCA T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:87726159..87727750 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine 117163 RMVar_ID_117163 Human_SNP_ID_878668405 m1A Human chr9 - 93259007 93259007 93259007 GTGGTGGCACGGGAGGCACAGTCGCGGTCGGCAGGTCTGGGAGGGCCGGAGGGAGGCCGTCGATT GTGGTGGCACGGGAGGCACAGTCGCGGTCGGCGGGTCTGGGAGGGCCGGAGGGAGGCCGTCGATT T C - - Other Unknown GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:93258957..93259229 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine 117164 RMVar_ID_117164 Human_SNP_ID_878681593 m1A Human chr9 - 41358967 41358967 41358967 GCTGGTCTCAGCCCCGACTCTGACGCACGATCACACAGGGCTCCTACTTCGCCAAGTCTCAGGGA GCTGGTCTCAGCCCCGACTCTGACGCACGATCTCACAGGGCTCCTACTTCGCCAAGTCTCAGGGA T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:41358917..41358985 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 117165 RMVar_ID_117165 Human_SNP_ID_878682508 m1A Human chr9 + 134139929 134139929 134139929 AGCCCGAGACCGAGGCCGCCAGAGCACAGCCAACCCCTTCGTCATCCGCCACTCAGAGCAAGGTG AGCCCGAGACCGAGGCCGCCAGAGCACAGCCACCCCCTTCGTCATCCGCCACTCAGAGCAAGGTG A C WDR5 Ensembl:ENSG00000196363 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:134139774..134139975 26863196 MeRIP-seq:(Medium) rs996722012 Functional Loss SNV ICGC 33..33 33 SKCA 3 - Human_RBP_ID_9407748,Human_RBP_ID_18472826 Human_Splice_Rec_1096889,Human_Splice_Rec_1096895,Human_Splice_Rec_1096903 Human_miRNA_ID_2384528,Human_miRNA_ID_2384529 RMVar_hsa_circ_47471,RMVar_hsa_circ_278837,RMVar_hsa_circ_86172,RMVar_hsa_circ_310348,RMVar_hsa_circ_260700,RMVar_hsa_circ_279062,RMVar_hsa_circ_89421,RMVar_hsa_circ_274086,RMVar_hsa_circ_48044,RMVar_hsa_circ_260701,RMVar_hsa_circ_9170,RMVar_hsa_circ_260702 117166 RMVar_ID_117166 Human_SNP_ID_878694283 m1A Human chr9 + 134158417 134158417 134158417 GTGGCCCCGCCAGCTGGCCTCCCCTTTGGCCCACGCCGGCCGCCCCCATTCTCTGCTGCGTAGAT GTGGCCCCGCCAGCTGGCCTCCCCTTTGGCCCTCGCCGGCCGCCCCCATTCTCTGCTGCGTAGAT A T WDR5 Ensembl:ENSG00000196363 Protein coding 3'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134158371..134158439 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_8224735,Human_RBP_ID_18131966,Human_RBP_ID_22337375,Human_RBP_ID_26565587,Human_RBP_ID_26834472,Human_RBP_ID_27543770 Human_miRNA_ID_2386763,Human_miRNA_ID_2388238,Human_miRNA_ID_2399390,Human_miRNA_ID_3030441 RMVar_hsa_circ_117469,RMVar_hsa_circ_260710 117167 RMVar_ID_117167 Human_SNP_ID_878695738 m1A Human chr9 - 128632933 128632933 128632933 AGGCCCATACCTGGTAGAGCTCCTCCTTGGTCACGTAAGGCTTTCCCTCTGAGCTGAGGGCCCGG AGGCCCATACCTGGTAGAGCTCCTCCTTGGTCTCGTAAGGCTTTCCCTCTGAGCTGAGGGCCCGG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:128632882..128632957 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 7 brain Human_RBP_ID_16585620,Human_RBP_ID_22335873 117168 RMVar_ID_117168 Human_SNP_ID_878701809 m1A Human chr9 - 37948706 37948706 37948706 ATCAGCAGAGGAGACGCCGAGAACCTGCTGCGACTCTGCAAGGAGTGTAGCTACCTTGTCCGGAA ATCAGCAGAGGAGACGCCGAGAACCTGCTGCGTCTCTGCAAGGAGTGTAGCTACCTTGTCCGGAA T A SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding CDS,3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:37948657..37955985 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary Human_RBP_ID_1227460,Human_RBP_ID_22838708 Human_Splice_Rec_1044766,Human_Splice_Rec_1044767,Human_Splice_Rec_1045040,Human_Splice_Rec_1045041 Human_miRNA_ID_1389995,Human_miRNA_ID_1389996 RMVar_hsa_circ_256957,RMVar_hsa_circ_297965,RMVar_hsa_circ_311485,RMVar_hsa_circ_256959,RMVar_hsa_circ_291058,RMVar_hsa_circ_256958 117169 RMVar_ID_117169 Human_SNP_ID_878711536 m1A Human chr9 + 131470840 131470840 131470840 GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCACCCCCAGCGCACCTTTTACCCACACCACCCCC GCACTGGCAGCCGGTGTACCCCCCGCCGTCCCCCCCCCAGCGCACCTTTTACCCACACCACCCCC A C PRRC2B Ensembl:ENSG00000130723 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131470764..131471003 26863196 MeRIP-seq:(Medium) rs1398997491 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_90929,Human_RBP_ID_713770 Human_Splice_Rec_1092156,Human_Splice_Rec_1092228,Human_Splice_Rec_1092274 Human_miRNA_ID_2143493,Human_miRNA_ID_2145024,Human_miRNA_ID_2684412,Human_miRNA_ID_2687529 RMVar_hsa_circ_3344,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_56692,RMVar_hsa_circ_30116,RMVar_hsa_circ_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_122318,RMVar_hsa_circ_127170,RMVar_hsa_circ_108160,RMVar_hsa_circ_260448,RMVar_hsa_circ_260450,RMVar_hsa_circ_79982,RMVar_hsa_circ_260451,RMVar_hsa_circ_260449,RMVar_hsa_circ_260447,RMVar_hsa_circ_84564,RMVar_hsa_circ_42629,RMVar_hsa_circ_124987,RMVar_hsa_circ_260456,RMVar_hsa_circ_127632,RMVar_hsa_circ_118178,RMVar_hsa_circ_260459,RMVar_hsa_circ_260460,RMVar_hsa_circ_260461,RMVar_hsa_circ_76928,RMVar_hsa_circ_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260462,RMVar_hsa_circ_109752,RMVar_hsa_circ_321160,RMVar_hsa_circ_11680,RMVar_hsa_circ_85168,RMVar_hsa_circ_260468,RMVar_hsa_circ_260470,RMVar_hsa_circ_260469 117170 RMVar_ID_117170 Human_SNP_ID_878715652 m1A Human chr9 + 107324887 107324887 107324887 CATTTTATTCAGATGTTAAATGAACCAGTTCAAGAAGCTGGTGGTCAAGGAGGAGGAGGTGGAGG CATTTTATTCAGATGTTAAATGAACCAGTTCAGGAAGCTGGTGGTCAAGGAGGAGGAGGTGGAGG A G - - Other Unknown GSE97419:GSM2564289,GSM2564290,GSM2564291,GSM2564292 HEK293T cells, overexperss TRMT6 - 29072297 m1A-MAP:(High) rs753505436 Functional Loss SNV ICGC 33..33 33 LICA 1 - 117171 RMVar_ID_117171 Human_SNP_ID_878715811 m1A Human chr9 - 129722321 129722321 129722321 TTCAGTTCACCGTAGGCACCTGGCTGTGGTGCAGGCTGAACTCCTTGGCCTTGAGACGGAGGCTG TTCAGTTCACCGTAGGCACCTGGCTGTGGTGCCGGCTGAACTCCTTGGCCTTGAGACGGAGGCTG T G RF00017-4531 RNACentral:URS000098F531 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129722271..129722361 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 2 caecum,large intestine 117172 RMVar_ID_117172 Human_SNP_ID_878720725 m1A Human chr9 + 109835324 109835324 109835324 GGTGGGGGAAAGAGGGGAGGGTGGAGAGATGGAGAGGAGGGTGGAGGGATAGAGGAAAGGGTGGA GGTGGGGGAAAGAGGGGAGGGTGGAGAGATGGGGAGGAGGGTGGAGGGATAGAGGAAAGGGTGGA A G PALM2AKAP2 Ensembl:ENSG00000157654 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:109835320..109835439 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_321422 117173 RMVar_ID_117173 Human_SNP_ID_878723596 m1A Human chr9 - 70259016 70258993 70259017 CCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGCG CCGTTCCCACCGTCCGGCAGCCCAGGCGCCC________________________CGCTCCCGCG GGGGCGCCTGGGTGGATGGGCGCTT G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:70258973..70259143 26863196 MeRIP-seq:(Medium) rs1344863756 Functional Loss DEL ICGC 32..55 33 PAAD 1 - 117174 RMVar_ID_117174 Human_SNP_ID_878723596 m1A Human chr9 - 70259017 70258993 70259017 TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCCAAGCGCCCATCCACCCAGGCGCCCCGCTCCCGC TCCGTTCCCACCGTCCGGCAGCCCAGGCGCCC________________________CGCTCCCGC GGGGCGCCTGGGTGGATGGGCGCTT G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:70258972..70259151 26863196 MeRIP-seq:(Medium) rs1344863756 Functional Loss DEL ICGC 33..56 33 PAAD 1 - 117175 RMVar_ID_117175 Human_SNP_ID_878725444 m1A Human chr9 - 98119152 98119152 98119152 CGGGCGCGGCGACCGGGAGCCGGACCCCTGGGAGGTCGGAGCTTGTCGAGGGATGCGGCTGGCGC CGGGCGCGGCGACCGGGAGCCGGACCCCTGGGTGGTCGGAGCTTGTCGAGGGATGCGGCTGGCGC T A TRIM14 Ensembl:ENSG00000106785 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:98119104..98119265 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_256529,Human_RBP_ID_798581,Human_RBP_ID_5154962,Human_RBP_ID_23094616,Human_RBP_ID_26360906 RMVar_hsa_circ_54087 117176 RMVar_ID_117176 Human_SNP_ID_878734466 m1A Human chr9 + 97854452 97854446 97854452 CCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCATCTTCCCAGGCGCGGTGCCCGCCGCGCGCCCC CCGCCGCCGCCGCCGCCGCCGCCGCCG______TCTTCCCAGGCGCGGTGCCCGCCGCGCGCCCC GCCGCCA G FOXE1 Ensembl:ENSG00000178919 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:97854390..97854490 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 28..33 33 LMS 2 - 117177 RMVar_ID_117177 Human_SNP_ID_878735033 m1A Human chr9 - 134738457 134738457 134738457 CCTCGATGAGCATGCCCTGGGGAGACAGAGAGAGGGCGTCTGAGACCGCAGCCCATCCCTCCCGA CCTCGATGAGCATGCCCTGGGGAGACAGAGAGGGGGCGTCTGAGACCGCAGCCCATCCCTCCCGA T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134738451..134738500 26863196 MeRIP-seq:(Medium) rs767955467 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 117178 RMVar_ID_117178 Human_SNP_ID_878751836 m1A Human chr9 - 127523826 127523826 127523826 CTGTCTCCACAGGGACCACGGCAAAGTCGGGCAGTGCCCCCATCCTCAAGTGCCCCACACAGTTC CTGTCTCCACAGGGACCACGGCAAAGTCGGGCGGTGCCCCCATCCTCAAGTGCCCCACACAGTTC T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:127523776..127523850 26863196 MeRIP-seq:(Medium) rs944462596 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1226145 Human_Splice_Rec_1082272,Human_Splice_Rec_1082302 Human_miRNA_ID_1025230,Human_miRNA_ID_2466495 RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_259765,RMVar_hsa_circ_122231,RMVar_hsa_circ_7962,RMVar_hsa_circ_122936,RMVar_hsa_circ_98775,RMVar_hsa_circ_259768,RMVar_hsa_circ_259769,RMVar_hsa_circ_346970,RMVar_hsa_circ_91870,RMVar_hsa_circ_48174,RMVar_hsa_circ_259771,RMVar_hsa_circ_259772,RMVar_hsa_circ_357415,RMVar_hsa_circ_43685,RMVar_hsa_circ_343610,RMVar_hsa_circ_259773,RMVar_hsa_circ_259774,RMVar_hsa_circ_259775,RMVar_hsa_circ_275532,RMVar_hsa_circ_317016,RMVar_hsa_circ_259776 117179 RMVar_ID_117179 Human_SNP_ID_878753124 m1A Human chr9 + 133460781 133460781 133460781 GCACAGGTGGCCCCTGGGGCCGCGGGGCAGTGAGCTGAGGGCCCGGCCTCTCCCTGGGTCCTCTG GCACAGGTGGCCCCTGGGGCCGCGGGGCAGTGGGCTGAGGGCCCGGCCTCTCCCTGGGTCCTCTG A G CACFD1 Ensembl:ENSG00000160325 Protein coding intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:133460779..133460898 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 117180 RMVar_ID_117180 Human_SNP_ID_878753902 m1A Human chr9 - 173218 173218 173218 TGTACATGGTTTACTAGAAATGTTTATTGATTATATTTCCAGCTTTAATTTTCTTGAGTAATTTA TGTACATGGTTTACTAGAAATGTTTATTGATTGTATTTCCAGCTTTAATTTTCTTGAGTAATTTA T C CBWD1 Ensembl:ENSG00000172785 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1554633552 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_miRNA_ID_155594,Human_miRNA_ID_898797,Human_miRNA_ID_905458,Human_miRNA_ID_912100,Human_miRNA_ID_918732,Human_miRNA_ID_1120949,Human_miRNA_ID_1128088,Human_miRNA_ID_1216151,Human_miRNA_ID_1282330 RMVar_hsa_circ_2994,RMVar_hsa_circ_73448,RMVar_hsa_circ_255221,RMVar_hsa_circ_333643 117181 RMVar_ID_117181 Human_SNP_ID_878754384 m1A Human chr9 - 35077324 35077324 35077324 GTCCCCCAGCTGAGGAATTAGATGCTCCATTGACCCTGCAGGATGCCCAGGGATTGAAGGATGTC GTCCCCCAGCTGAGGAATTAGATGCTCCATTGGCCCTGCAGGATGCCCAGGGATTGAAGGATGTC T C FANCG Ensembl:ENSG00000221829 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35076999..35077360 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_RBP_ID_8704119,Human_RBP_ID_23092396 Human_Splice_Rec_1040636,Human_Splice_Rec_1040637,Human_Splice_Rec_1040664,Human_Splice_Rec_1040665,Human_Splice_Rec_1040696 RMVar_hsa_circ_15124,RMVar_hsa_circ_32496 117182 RMVar_ID_117182 Human_SNP_ID_878759890 m1A Human chr9 - 21974809 21974798 21974809 CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGGAGCAGCATGGAGCCTTCGGCTGACTGGCTGGCC CGGCGGGGAGCAGCATGGAGCCGGCGGCGGGG___________GCCTTCGGCTGACTGGCTGGCC CTCCATGCTGCT C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:21974720..21974890 26863410 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..43 33 ESCA 1 - Human_RBP_ID_92522,Human_RBP_ID_5024668 117183 RMVar_ID_117183 Human_SNP_ID_878767499 m1A Human chr9 - 137163318 137163318 137163318 GCGGGCGCACGGACACTCACTTGAGGATGGACAGGGAGACGTTCTGCTTCCAGGGGCTGTCTTTG GCGGGCGCACGGACACTCACTTGAGGATGGACTGGGAGACGTTCTGCTTCCAGGGGCTGTCTTTG T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137163315..137163644 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 lung acinar_adenocarcinoma 7 lung 117184 RMVar_ID_117184 Human_SNP_ID_878768557 m1A Human chr9 - 137050096 137050096 137050096 TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTAAGGGCAGGCGGGTGGCTGGGAACTTTGTCGTGA TAGGCGGGTGGCTGGGAACTTTGTCGTGGGTAGGGGCAGGCGGGTGGCTGGGAACTTTGTCGTGA T C ENTPD2 Ensembl:ENSG00000054179 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137050026..137050200;chr9:137050038..137050156;chr9:137050017..137050319 26863196 MeRIP-seq:(Medium) rs12555382 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_846398,Human_RBP_ID_3908421,Human_RBP_ID_8224384,Human_RBP_ID_8239490,Human_RBP_ID_9441884,Human_RBP_ID_18962602,Human_RBP_ID_19146588,Human_RBP_ID_21996179,Human_RBP_ID_22419590,Human_RBP_ID_22705034,Human_RBP_ID_26796884 117185 RMVar_ID_117185 Human_SNP_ID_878776012 m1A Human chr9 + 21974699 21974699 21974699 CCTCTACCCACCTGGATCGGCCTCCGACCGTAACTATTCGGTGCGTTGGGCAGCGCCCCCGCCTC CCTCTACCCACCTGGATCGGCCTCCGACCGTATCTATTCGGTGCGTTGGGCAGCGCCCCCGCCTC A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21974691..21975024 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 7 ovary 117186 RMVar_ID_117186 Human_SNP_ID_878783839 m1A Human chr9 + 130809417 130809417 130809417 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT A T ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130809393..130809490 26863196 MeRIP-seq:(Medium) rs2855185 Functional Loss SNV ICGC,COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,COCA,central_nervous_system astrocytoma_Grade_III,large_intestine adenocarcinoma 3 large intestine,brain Human_RBP_ID_9352029,Human_RBP_ID_24289379 RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 117187 RMVar_ID_117187 Human_SNP_ID_878785940 m1A Human chr9 - 127663355 127663355 127663355 GAGGCCACTCCAGCAGACTGGTGCACTGCCTTACCCCCGATACCGCACAGCCGGGTACTCCTTCA GAGGCCACTCCAGCAGACTGGTGCACTGCCTTTCCCCCGATACCGCACAGCCGGGTACTCCTTCA T A RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127663328..127663428 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 28 liver 117188 RMVar_ID_117188 Human_SNP_ID_878786899 m1A Human chr9 + 35060451 35060451 35060451 GCTTTGGCCAACAAAGTTTTCCCACAGCCAGGAGGTCCATAGAACAGAACTCCCTTGGAAGGTGT GCTTTGGCCAACAAAGTTTTCCCACAGCCAGGTGGTCCATAGAACAGAACTCCCTTGGAAGGTGT A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:35060301..35060450 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 117189 RMVar_ID_117189 Human_SNP_ID_878798954 m1A Human chr9 - 126346768 126346768 126346768 TTTTCCCCTTAGTTTTCTTTAATTTTCCACCTACCTCTCCAGATGCTCAGGCTTAGTCCCCTTTT TTTTCCCCTTAGTTTTCTTTAATTTTCCACCTGCCTCTCCAGATGCTCAGGCTTAGTCCCCTTTT T C - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:126346764..126346896 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 117190 RMVar_ID_117190 Human_SNP_ID_878802504 m1A Human chr9 + 33262801 33262801 33262801 TTGGACAACTGGTTCACTGCTGCCCTGCTGGGAGGTAACATGAAGGTCGTGCTTCTCATTGCCTG TTGGACAACTGGTTCACTGCTGCCCTGCTGGGGGGTAACATGAAGGTCGTGCTTCTCATTGCCTG A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:33262751..33262800 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_256334 117191 RMVar_ID_117191 Human_SNP_ID_878817961 m1A Human chr9 - 86323106 86323106 86323106 ATGGCATGGCTAATGAAGATGAGTTAGACAACACCTACACTGGGTCAGGGGATGAGGACGCCCTA ATGGCATGGCTAATGAAGATGAGTTAGACAACGCCTACACTGGGTCAGGGGATGAGGACGCCCTA T C TUT7 Ensembl:ENSG00000083223 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:86323055..86323140 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 READ 2 - Human_RBP_ID_22119282,Human_RBP_ID_24549599,Human_RBP_ID_27833132 RMVar_hsa_circ_367806,RMVar_hsa_circ_63121,RMVar_hsa_circ_53082,RMVar_hsa_circ_55923,RMVar_hsa_circ_30555,RMVar_hsa_circ_257612,RMVar_hsa_circ_58537,RMVar_hsa_circ_359058,RMVar_hsa_circ_359751,RMVar_hsa_circ_47200,RMVar_hsa_circ_257620,RMVar_hsa_circ_353569,RMVar_hsa_circ_257622,RMVar_hsa_circ_322445,RMVar_hsa_circ_257623,RMVar_hsa_circ_355889,RMVar_hsa_circ_361843,RMVar_hsa_circ_14937,RMVar_hsa_circ_266681,RMVar_hsa_circ_354884 117192 RMVar_ID_117192 Human_SNP_ID_878841730 m1A Human chr9 - 15466796 15466796 15466796 TCAAGATGGTAATCAGCCACAACATAACGGGGAGAGCAATGAAGACAGCAAAGACAACCATGAAG TCAAGATGGTAATCAGCCACAACATAACGGGGGGAGCAATGAAGACAGCAAAGACAACCATGAAG T C PSIP1 Ensembl:ENSG00000164985 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:15466726..15466850 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_91602,Human_RBP_ID_256188,Human_RBP_ID_26360594 Human_Splice_Rec_1033692,Human_Splice_Rec_1033693,Human_Splice_Rec_1033722,Human_Splice_Rec_1033723 RMVar_hsa_circ_59570,RMVar_hsa_circ_98452,RMVar_hsa_circ_114356,RMVar_hsa_circ_255823,RMVar_hsa_circ_87910,RMVar_hsa_circ_255824,RMVar_hsa_circ_255822 117193 RMVar_ID_117193 Human_SNP_ID_878849688 m1A Human chr9 + 21970974 21970974 21970974 GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTACCGTGCGACATCGCGATGGCCCAGCTCCTCAG GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTTCCGTGCGACATCGCGATGGCCCAGCTCCTCAG A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970951..21970975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 12 uterus 117194 RMVar_ID_117194 Human_SNP_ID_878849724 m1A Human chr9 + 21970974 21970974 21970974 GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTACCGTGCGACATCGCGATGGCCCAGCTCCTCAG GCCTCTGGTGCCCCCCGCAGCCGCGCGCAGGTGCCGTGCGACATCGCGATGGCCCAGCTCCTCAG A G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:21970951..21970975 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 10 ovary 117195 RMVar_ID_117195 Human_SNP_ID_878851498 m1A Human chr9 + 128261560 128261560 128261560 TCTCCATTTGTAGTTGTCTAACCGACTCCATTACCTGCAAGAATGGCCACAGAAATGAGGAAGGA TCTCCATTTGTAGTTGTCTAACCGACTCCATTCCCTGCAAGAATGGCCACAGAAATGAGGAAGGA A C RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128261526..128261575 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 cervix squamous_cell_carcinoma 4 uterus 117196 RMVar_ID_117196 Human_SNP_ID_878854430 m1A Human chr9 + 137110937 137110937 137110937 CCTGGATGGTGACGGCGATGACTGAGGCACTCAGGTTCCTCCGAATCTGTGGTCAGTGGAAAGAA CCTGGATGGTGACGGCGATGACTGAGGCACTCGGGTTCCTCCGAATCTGTGGTCAGTGGAAAGAA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137110876..137110975 32194978 MeRIP-seq:(Medium) rs761585241 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine 117197 RMVar_ID_117197 Human_SNP_ID_878855108 m1A Human chr9 + 22008984 22008984 22008984 ATTCCGCAGCCCCCAGACGCGCAGCGGCCCGGATAATCCACCGTTGGCCGTAAACTTAACGACAC ATTCCGCAGCCCCCAGACGCGCAGCGGCCCGGGTAATCCACCGTTGGCCGTAAACTTAACGACAC A G AL359922.1,CDKN2B-AS1 Ensembl:ENSG00000264545,Ensembl:ENSG00000240498 Protein coding,lincRNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:22008826..22009300;chr9:22008771..22009300 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_256182,RMVar_hsa_circ_111947 117198 RMVar_ID_117198 Human_SNP_ID_878856372 m1A Human chr9 + 127898911 127898911 127898911 GGGGAGCGGCTTGCTCACGCTGGGGAGGCGGCAGCCCCGAGCGCTGGGCCAGGAGCATGGACTCA GGGGAGCGGCTTGCTCACGCTGGGGAGGCGGCCGCCCCGAGCGCTGGGCCAGGAGCATGGACTCA A C RF00017-4498 RNACentral:URS0000930330 SRP RNA intron GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:127898904..127899066 32194978 MeRIP-seq:(Medium) rs569431080 Functional Loss SNV ICGC 33..33 33 MALY 1 - 117199 RMVar_ID_117199 Human_SNP_ID_878863042 m1A Human chr9 + 137167576 137167576 137167576 TCCTCTGCCCCCTCCCCCGCAGACAGACAGACAGACGGACGGGACAGCGGCCCGGCCCACGCAGA TCCTCTGCCCCCTCCCCCGCAGACAGACAGACGGACGGACGGGACAGCGGCCCGGCCCACGCAGA A G GRIN1 Ensembl:ENSG00000176884 Protein coding 3'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:137167566..137167718 26863196 MeRIP-seq:(Medium) rs974552016 Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine 117200 RMVar_ID_117200 Human_SNP_ID_878867376 m1A Human chr9 - 34637627 34637627 34637627 GCTGCTCCTGGCTGTCGCAGCGGTGCTGACCCAGGTCGTCTGGCTCTGGCTGGGTACGCAGAGCT GCTGCTCCTGGCTGTCGCAGCGGTGCTGACCCGGGTCGTCTGGCTCTGGCTGGGTACGCAGAGCT T C SIGMAR1 Ensembl:ENSG00000147955 Protein coding 5'UTR GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:34637576..34637761 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_718234,Human_RBP_ID_798273,Human_RBP_ID_1705009,Human_RBP_ID_5027138,Human_RBP_ID_5124341,Human_RBP_ID_22466349,Human_RBP_ID_27136150,Human_RBP_ID_27162469,Human_RBP_ID_27374945,Human_RBP_ID_27545792 Human_Splice_Rec_1039819,Human_Splice_Rec_1039825,Human_Splice_Rec_1039831,Human_Splice_Rec_1039837 117201 RMVar_ID_117201 Human_SNP_ID_878873953 m1A Human chr9 + 135503889 135503889 135503889 ACACGTGGCCGTGAGAGACGCAGCCAAGATGAACATCCCCACAGTGGGCATCGTGGACACCAACT ACACGTGGCCGTGAGAGACGCAGCCAAGATGAGCATCCCCACAGTGGGCATCGTGGACACCAACT A G MRPS2 Ensembl:ENSG00000122140 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135503839..135503920 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_714754,Human_RBP_ID_5018556,Human_RBP_ID_17321648,Human_RBP_ID_17435886,Human_RBP_ID_18197025,Human_RBP_ID_26562341,Human_RBP_ID_27372620,Human_RBP_ID_27543966 Human_miRNA_ID_2725651 RMVar_hsa_circ_124833,RMVar_hsa_circ_82747,RMVar_hsa_circ_260773,RMVar_hsa_circ_104717,RMVar_hsa_circ_260774,RMVar_hsa_circ_260775 117202 RMVar_ID_117202 Human_SNP_ID_878877391 m1A Human chr9 + 130476912 130476912 130476912 CCTCCAGGTCTCTACACGAAGACCCAGGACCCAGCCAAAGCCCCCAACACCCCTGACATTCTCGA CCTCCAGGTCTCTACACGAAGACCCAGGACCCCGCCAAAGCCCCCAACACCCCTGACATTCTCGA A C ASS1 Ensembl:ENSG00000130707 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c chr9:130476814..130477003;chr9:130476901..130476925 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_27543012 Human_Splice_Rec_1090880,Human_Splice_Rec_1090881,Human_Splice_Rec_1090910,Human_Splice_Rec_1090911,Human_Splice_Rec_1090940,Human_Splice_Rec_1090941,Human_Splice_Rec_1090986,Human_Splice_Rec_1090987,Human_Splice_Rec_1090994,Human_Splice_Rec_1091000,Human_Splice_Rec_1091001,Human_Splice_Rec_1091007 RMVar_hsa_circ_366782,RMVar_hsa_circ_353291,RMVar_hsa_circ_115689,RMVar_hsa_circ_34517,RMVar_hsa_circ_33466,RMVar_hsa_circ_260322,RMVar_hsa_circ_260323,RMVar_hsa_circ_44540,RMVar_hsa_circ_369228,RMVar_hsa_circ_31218,RMVar_hsa_circ_366636,RMVar_hsa_circ_70354,RMVar_hsa_circ_260330,RMVar_hsa_circ_309553,RMVar_hsa_circ_340138,RMVar_hsa_circ_260329 117203 RMVar_ID_117203 Human_SNP_ID_878878543 m1A Human chr9 + 137453150 137453150 137453150 TGTCCCAGTCCAGGTCCTCGAAGGCCTCGTCCAGCGTGCAGTGGGAGCTCTGCAGGTCACTGCCT TGTCCCAGTCCAGGTCCTCGAAGGCCTCGTCCTGCGTGCAGTGGGAGCTCTGCAGGTCACTGCCT A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:137453126..137453150 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 6 breast 117204 RMVar_ID_117204 Human_SNP_ID_878890625 m1A Human chr9 - 95516662 95516662 95516662 GGAGAAGAAGAAGAAGAAAACGGAGGAGAAGAAAAAGACGACAGGGGAGACAAAGAGACCCGCAG GGAGAAGAAGAAGAAGAAAACGGAGGAGAAGAGAAAGACGACAGGGGAGACAAAGAGACCCGCAG T C PTCH1 Ensembl:ENSG00000185920 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:95516491..95516712 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus 117205 RMVar_ID_117205 Human_SNP_ID_878907204 m1A Human chr9 - 35074977 35074977 35074977 TAGTCGTGGACTGGAATGGGTAGCCAGCGGCCAGGATACCAAAGCCTTACAGGACTTCCTCCTCA TAGTCGTGGACTGGAATGGGTAGCCAGCGGCCGGGATACCAAAGCCTTACAGGACTTCCTCCTCA T C FANCG Ensembl:ENSG00000221829 Protein coding 3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:35074889..35075012 26863196 MeRIP-seq:(Medium) rs1416054222 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_18135492 Human_Splice_Rec_1040651,Human_Splice_Rec_1040679 RMVar_hsa_circ_82931,RMVar_hsa_circ_94712,RMVar_hsa_circ_119528,RMVar_hsa_circ_256550,RMVar_hsa_circ_256551,RMVar_hsa_circ_103352,RMVar_hsa_circ_256552,RMVar_hsa_circ_256553 117206 RMVar_ID_117206 Human_SNP_ID_878912198 m1A Human chr9 - 128828842 128828840 128828842 GTTCTTTTATCCAGAGAAAGAGGAGAAAAAAAAATGGAAGGATCTCAAGCTGATGAAAAAACTGG GTTCTTTTATCCAGAGAAAGAGGAGAAAAAAA__TGGAAGGATCTCAAGCTGATGAAAAAACTGG ATT A SPOUT1,AL441992.3 Ensembl:ENSG00000198917,Ensembl:ENSG00000286112 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1782898,GSM1782899,GSM1782900,GSM1782901 HEK293T cell line,total RNA chr9:128828792..128828915 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..34 33 STAD 1 - Human_RBP_ID_9407627,Human_RBP_ID_24288124,Human_RBP_ID_26361231,Human_RBP_ID_27832825 Human_Splice_Rec_1087894,Human_Splice_Rec_1087930,Human_Splice_Rec_1087980 117207 RMVar_ID_117207 Human_SNP_ID_878917755 m1A Human chr9 + 120714022 120714022 120714022 CGAGGGGCCGAGCGGCGCCTGAAAGGTGGTGGAAGAGGGTCCAGCAGTCGCCCAAAGAGGGGTGG CGAGGGGCCGAGCGGCGCCTGAAAGGTGGTGGCAGAGGGTCCAGCAGTCGCCCAAAGAGGGGTGG A C - - Other Unknown GSE70485:GSM1782894,GSM1782895 HEPG2 cell line,total RNA rearranged at 60c chr9:120713973..120714161 26863196 MeRIP-seq:(Medium) rs201403181 Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach 117208 RMVar_ID_117208 Human_SNP_ID_878923305 m1A Human chr9 + 34660726 34660726 34660726 CTGAACCTGTCTGATTCTGGAACTACCTCCCCATACCTCCATCCCCCATGCCCCACTTGATTTTA CTGAACCTGTCTGATTCTGGAACTACCTCCCCCTACCTCCATCCCCCATGCCCCACTTGATTTTA A C IL11RA Ensembl:ENSG00000137070 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34660712..34660782 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 117209 RMVar_ID_117209 Human_SNP_ID_878989802 m1A Human chr9 + 128437297 128437297 128437297 GTACAGGGAGGTAAAGCAGGACCCTTGCAGACATGTTGCCCAGCACACAGTAGGCCCTCAATAAA GTACAGGGAGGTAAAGCAGGACCCTTGCAGACCTGTTGCCCAGCACACAGTAGGCCCTCAATAAA A C CERCAM Ensembl:ENSG00000167123 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs6918 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_185202,Human_RBP_ID_17323487,Human_RBP_ID_18963114 GWAS_ID_14730,GWAS_ID_14731,GWAS_ID_14732,GWAS_ID_14733,GWAS_ID_14734,GWAS_ID_14735,GWAS_ID_14736,GWAS_ID_14737 117210 RMVar_ID_117210 Human_SNP_ID_878991091 m1A Human chr9 - 113275762 113275762 113275762 GAGCTGGGATCCCGGGCTCTGTACCGTGGAAGAGGCTCGCGAGGAAGCCATGCTGGGCTCTGGAG GAGCTGGGATCCCGGGCTCTGTACCGTGGAAGTGGCTCGCGAGGAAGCCATGCTGGGCTCTGGAG T A RF00017-4706 RNACentral:URS0000954994 SRP RNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:113275711..113275806 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus 117211 RMVar_ID_117211 Human_SNP_ID_878999241 m1A Human chr9 + 21974759 21974755 21974759 GCCTCCAGCAGCGCCCGCACCTCCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC GCCTCCAGCAGCGCCCGCACCTCCTCTAC____CCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGC CCCGA C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:21974676..21975075 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA,ICGC 30..33 33 HNSC 2 - 117212 RMVar_ID_117212 Human_SNP_ID_879004165 m1A Human chr9 + 130809417 130809416 130809418 AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGTGTGTGTGTGTGTGTGTGTGTGTGTGCACGT AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAG__TGTGTGTGTGTGTGTGTGTGTGTGTGCACGT GAG G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130809393..130809490 26863196 MeRIP-seq:(Medium) - Functional Loss DEL ICGC 33..34 33 LMS 1 - Human_RBP_ID_9352029,Human_RBP_ID_24289379 RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 117213 RMVar_ID_117213 Human_SNP_ID_879009459 m1A Human chr9 - 135818578 135818576 135818579 AGCTGAGGAAGACCGGGTGCGGAAGGAGGAGGAGAAGGCGCGGCGCGAGCTCATCAAGCAGGAGT AGCTGAGGAAGACCGGGTGCGGAAGGAGGAG___AAGGCGCGGCGCGAGCTCATCAAGCAGGAGT TCTC T CAMSAP1 Ensembl:ENSG00000130559 Protein coding CDS GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:135818528..135819101 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_Splice_Rec_1098722,Human_Splice_Rec_1098748,Human_Splice_Rec_1098764,Human_Splice_Rec_1098798,Human_Splice_Rec_1098814 RMVar_hsa_circ_49573,RMVar_hsa_circ_51530,RMVar_hsa_circ_265265,RMVar_hsa_circ_342118,RMVar_hsa_circ_265460,RMVar_hsa_circ_105500,RMVar_hsa_circ_83068,RMVar_hsa_circ_260777,RMVar_hsa_circ_260778,RMVar_hsa_circ_341302,RMVar_hsa_circ_99970,RMVar_hsa_circ_260779,RMVar_hsa_circ_34482,RMVar_hsa_circ_260780 117214 RMVar_ID_117214 Human_SNP_ID_879022110 m1A Human chr9 - 4727310 4727310 4727310 TTCAATGTAAACGAAACAGCCTTCTATTGGAAAAAGATGCCATCTAGGACTTCCATTGCTGGAGA TTCAATGTAAACGAAACAGCCTTCTATTGGAAGAAGATGCCATCTAGGACTTCCATTGCTGGAGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs4500134 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver Human_RBP_ID_3216000 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 117215 RMVar_ID_117215 Human_SNP_ID_879048867 m1A Human chr9 + 128288739 128288739 128288739 GAATGACTGAGCAGGCTCATCGCCCCTTGTCCACAGCTCCCAGGGACAGAAGGGTGTGGACATGA GAATGACTGAGCAGGCTCATCGCCCCTTGTCCGCAGCTCCCAGGGACAGAAGGGTGTGGACATGA A G SWI5 Ensembl:ENSG00000175854 Protein coding 3'UTR GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:128288689..128288790 32194978 MeRIP-seq:(Medium) rs181209395 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_712488,Human_RBP_ID_17666582,Human_RBP_ID_24287591 Human_Splice_Rec_1085866,Human_Splice_Rec_1085876,Human_Splice_Rec_1085884,Human_Splice_Rec_1085892,Human_Splice_Rec_1085918 RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_92526,RMVar_hsa_circ_126252,RMVar_hsa_circ_259893,RMVar_hsa_circ_83200,RMVar_hsa_circ_259894,RMVar_hsa_circ_259895,RMVar_hsa_circ_259896 117216 RMVar_ID_117216 Human_SNP_ID_879077809 m1A Human chr9 - 125148028 125148028 125148028 GCTCCTTACATAGTTTTTAATTATATAGCTATATGAAAGAGGTGGCTAAGACATTTGCTGCACAC GCTCCTTACATAGTTTTTAATTATATAGCTATCTGAAAGAGGTGGCTAAGACATTTGCTGCACAC T G PPP6C Ensembl:ENSG00000119414 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs1549314 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3188015,Human_RBP_ID_24522203,Human_RBP_ID_26560724 GWAS_ID_14661,GWAS_ID_14662,GWAS_ID_14663,GWAS_ID_14664,GWAS_ID_14665,GWAS_ID_14666,GWAS_ID_14667,GWAS_ID_14668,GWAS_ID_14669,GWAS_ID_14670,GWAS_ID_14671,GWAS_ID_14672,GWAS_ID_14673,GWAS_ID_14674,GWAS_ID_14675,GWAS_ID_14676,GWAS_ID_14677,GWAS_ID_14678,GWAS_ID_14679,GWAS_ID_14680,GWAS_ID_14681,GWAS_ID_14682,GWAS_ID_14683,GWAS_ID_14684,GWAS_ID_14685,GWAS_ID_14686,GWAS_ID_14687,GWAS_ID_14688,GWAS_ID_14689,GWAS_ID_14690,GWAS_ID_14691,GWAS_ID_14692,GWAS_ID_14693,GWAS_ID_14694,GWAS_ID_14695,GWAS_ID_14696,GWAS_ID_14697,GWAS_ID_14698,GWAS_ID_14699,GWAS_ID_14700,GWAS_ID_14701,GWAS_ID_14702,GWAS_ID_14703,GWAS_ID_14704,GWAS_ID_14705,GWAS_ID_14706,GWAS_ID_14707,GWAS_ID_14708,GWAS_ID_14709,GWAS_ID_14710,GWAS_ID_14711,GWAS_ID_14712,GWAS_ID_14713,GWAS_ID_14714,GWAS_ID_14715,GWAS_ID_14716,GWAS_ID_14717,GWAS_ID_14718,GWAS_ID_14719,GWAS_ID_14720,GWAS_ID_14721,GWAS_ID_14722,GWAS_ID_14723,GWAS_ID_14724,GWAS_ID_14725 117217 RMVar_ID_117217 Human_SNP_ID_879097433 m1A Human chr9 + 78304823 78304823 78304823 TCAGTGCTGTCCCCTTAAACCTCATTGGCTTGAAAGCAGGAAGGTGTGCTGACTATGTGGTGACA TCAGTGCTGTCCCCTTAAACCTCATTGGCTTGGAAGCAGGAAGGTGTGCTGACTATGTGGTGACA A G PSAT1 Ensembl:ENSG00000135069 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:78304773..78306445 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5043414,Human_RBP_ID_16703905,Human_RBP_ID_18910247,Human_RBP_ID_22467299,Human_RBP_ID_24307897 Human_Splice_Rec_1055354,Human_Splice_Rec_1055370 Human_miRNA_ID_1465354,Human_miRNA_ID_2742533 RMVar_hsa_circ_53541,RMVar_hsa_circ_126960,RMVar_hsa_circ_257299,RMVar_hsa_circ_95463,RMVar_hsa_circ_257298,RMVar_hsa_circ_331167,RMVar_hsa_circ_257300,RMVar_hsa_circ_257302,RMVar_hsa_circ_289514,RMVar_hsa_circ_335340,RMVar_hsa_circ_369901,RMVar_hsa_circ_257303,RMVar_hsa_circ_257301 117218 RMVar_ID_117218 Human_SNP_ID_879104189 m1A Human chr9 - 110137076 110137076 110137076 GCTGCTGCTGCTGCTGCTGTAACTGCTTCTGCAGCAGCAACTGTTCCTGCTGTGCCCTTCTCTCT GCTGCTGCTGCTGCTGCTGTAACTGCTTCTGCTGCAGCAACTGTTCCTGCTGTGCCCTTCTCTCT T A - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:110137026..110137126 32194978 MeRIP-seq:(Medium) rs1297414133 Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 5 stomach 117219 RMVar_ID_117219 Human_SNP_ID_879104465 m1A Human chr9 - 113597587 113597587 113597587 CTCTGTGTGTAGCCAGACTGCAGTGTCCCCCCAGGCTGCCTTAGTCCAGAAGGCCAGCTGCCTGC CTCTGTGTGTAGCCAGACTGCAGTGTCCCCCCCGGCTGCCTTAGTCCAGAAGGCCAGCTGCCTGC T G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:113597542..113597693 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 11 pancreas 117220 RMVar_ID_117220 Human_SNP_ID_879120516 m1A Human chr9 - 19376382 19376360 19376382 ACTGTTTGCTGTTTTGTTTTGTTTAGGAGGCTAAGGAGAAGCGCCAGGAACAAATTGCGAAGAGA ACTGTTTGCTGTTTTGTTTTGTTTAGGAGGCT______________________TTGCGAAGAGA ATTTGTTCCTGGCGCTTCTCCTT A RPS6 Ensembl:ENSG00000137154 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:19376369..19376475 26863196 MeRIP-seq:(Medium) - Functional Loss DEL TCGA 33..54 33 LIHC 1 - Human_RBP_ID_218259,Human_RBP_ID_256042,Human_RBP_ID_716610,Human_RBP_ID_797552,Human_RBP_ID_846699,Human_RBP_ID_964716,Human_RBP_ID_1058797,Human_RBP_ID_1146227,Human_RBP_ID_1704174,Human_RBP_ID_2062974,Human_RBP_ID_5041909,Human_RBP_ID_7913436,Human_RBP_ID_8701581,Human_RBP_ID_9234884,Human_RBP_ID_9406814,Human_RBP_ID_16634314,Human_RBP_ID_17666463,Human_RBP_ID_18140756,Human_RBP_ID_18907086,Human_RBP_ID_21709661,Human_RBP_ID_22119603,Human_RBP_ID_23141554,Human_RBP_ID_24549796,Human_RBP_ID_27134959 Human_Splice_Rec_1034890,Human_Splice_Rec_1034892,Human_Splice_Rec_1034900,Human_Splice_Rec_1034910 RMVar_hsa_circ_88413,RMVar_hsa_circ_122551,RMVar_hsa_circ_119085,RMVar_hsa_circ_120519,RMVar_hsa_circ_107449,RMVar_hsa_circ_255999,RMVar_hsa_circ_256001,RMVar_hsa_circ_256003,RMVar_hsa_circ_77164,RMVar_hsa_circ_256002,RMVar_hsa_circ_256000,RMVar_hsa_circ_255998 117221 RMVar_ID_117221 Human_SNP_ID_879127265 m1A Human chr9 - 134802964 134802964 134802964 CCTTCGTCCCTTCTTTTCCAGCAAGGCCCGGAAGCCCCTGTTCACCGGGGGGTCCAGGGGGCCCA CCTTCGTCCCTTCTTTTCCAGCAAGGCCCGGATGCCCCTGTTCACCGGGGGGTCCAGGGGGCCCA T A - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134802920..134803028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 117222 RMVar_ID_117222 Human_SNP_ID_879127281 m1A Human chr9 - 134802964 134802964 134802964 CCTTCGTCCCTTCTTTTCCAGCAAGGCCCGGAAGCCCCTGTTCACCGGGGGGTCCAGGGGGCCCA CCTTCGTCCCTTCTTTTCCAGCAAGGCCCGGACGCCCCTGTTCACCGGGGGGTCCAGGGGGCCCA T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134802920..134803028 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,ESCA,large_intestine adenocarcinoma 3 large intestine 117223 RMVar_ID_117223 Human_SNP_ID_879195615 m1A Human chr9 + 34989780 34989780 34989780 CCGGGTGGAGGCGGCGGAGCCGGAGCCGGGGGAGGGGGCAGCGGCTGTCTCACGGACCACGGCGG CCGGGTGGAGGCGGCGGAGCCGGAGCCGGGGGGGGGGGCAGCGGCTGTCTCACGGACCACGGCGG A G DNAJB5 Ensembl:ENSG00000137094 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:34989731..34989889 26863196 MeRIP-seq:(Medium) rs910884478 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_Splice_Rec_1040471,Human_Splice_Rec_1040479,Human_Splice_Rec_1040485,Human_Splice_Rec_1040489,Human_Splice_Rec_1040495 117224 RMVar_ID_117224 Human_SNP_ID_879207650 m1A Human chr9 + 21974781 21974781 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCTGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs864622263 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 9 lung Clinvar_Rec_187,Clinvar_Rec_188 117225 RMVar_ID_117225 Human_SNP_ID_879207680 m1A Human chr9 + 21974781 21974781 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCGGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC A G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,pancreas ductal_carcinoma,haematopoietic_and_lymphoid_tissue breast_implant_associated_anaplastic_large_cell_lymphoma_invasive,breast breast_implant_associated_anaplastic_large_cell_lymphoma_invasive 22 biliary tract,gallbladder,pancreas,haematopoietic and lymphoid tissue,breast 117226 RMVar_ID_117226 Human_SNP_ID_879207689 m1A Human chr9 + 21974781 21974781 21974781 CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCAGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC CCTCTACCCGACCCCGGGCCGCGGCCGTGGCCCGCCAGTCAGCCGAAGGCTCCATGCTGCTCCCC A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:21974735..21974842 26863410 MeRIP-seq:(Medium) rs864622263 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 9 stomach Clinvar_Rec_187,Clinvar_Rec_188 117227 RMVar_ID_117227 Human_SNP_ID_879210020 m1A Human chr9 + 111897241 111897241 111897241 CCGGGGGATGGCGCTGCTGGACCTGGCCTTGGAGGGAATGGCCGTCTTCGGGTTCGTCCTCTTCT CCGGGGGATGGCGCTGCTGGACCTGGCCTTGGTGGGAATGGCCGTCTTCGGGTTCGTCCTCTTCT A T UGCG Ensembl:ENSG00000148154 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:111896914..111897325 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_5006212,Human_RBP_ID_7888396,Human_RBP_ID_27541087 Human_Splice_Rec_1071813,Human_Splice_Rec_1071829,Human_Splice_Rec_1071831,Human_Splice_Rec_1071841 RMVar_hsa_circ_86759,RMVar_hsa_circ_258744 117228 RMVar_ID_117228 Human_SNP_ID_879251970 m1A Human chr9 - 37948727 37948727 37948727 CACAGATGGTATCACGGAGCCATCAGCAGAGGAGACGCCGAGAACCTGCTGCGACTCTGCAAGGA CACAGATGGTATCACGGAGCCATCAGCAGAGGGGACGCCGAGAACCTGCTGCGACTCTGCAAGGA T C SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding CDS,3'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:37948676..37948811 26863196 MeRIP-seq:(Medium) rs3827519 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,stomach adenocarcinoma,COCA,large_intestine adenocarcinoma 5 stomach,large intestine,breast Human_Splice_Rec_1044766,Human_Splice_Rec_1044767,Human_Splice_Rec_1045040,Human_Splice_Rec_1045041 Human_miRNA_ID_2017795,Human_miRNA_ID_2221414,Human_miRNA_ID_2484466,Human_miRNA_ID_3072843 GWAS_ID_7867,GWAS_ID_7868,GWAS_ID_7869,GWAS_ID_7870,GWAS_ID_7871,GWAS_ID_7872,GWAS_ID_7873,GWAS_ID_7874 RMVar_hsa_circ_256957,RMVar_hsa_circ_297965,RMVar_hsa_circ_311485,RMVar_hsa_circ_256959,RMVar_hsa_circ_291058,RMVar_hsa_circ_256958 117229 RMVar_ID_117229 Human_SNP_ID_879254236 m1A Human chr9 + 93672850 93672850 93672850 GTAGGTGTAGGAACAGGTGTAGATGCAGGTGCAGGGGTGGAGGTAGGTACAGGTGTAGATGCAGG GTAGGTGTAGGAACAGGTGTAGATGCAGGTGCGGGGGTGGAGGTAGGTACAGGTGTAGATGCAGG A G PHF2 Ensembl:ENSG00000197724 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93672804..93672953 26863196 MeRIP-seq:(Medium) rs1383843182 Functional Loss SNV ICGC 33..33 33 STAD 2 - Human_RBP_ID_5226685 117230 RMVar_ID_117230 Human_SNP_ID_879258384 m1A Human chr9 - 131739830 131739830 131739830 CTGTCGCCCCGCGGCGGCCCGGCCCGGGCCCGATGAGCGGCGGCCTCGGCCTCCGGCGCAGCCCG CTGTCGCCCCGCGGCGGCCCGGCCCGGGCCCGTTGAGCGGCGGCCTCGGCCTCCGGCGCAGCCCG T A RAPGEF1 Ensembl:ENSG00000107263 Protein coding start codon GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:131739785..131740094 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_5035943,Human_RBP_ID_9339139 Human_Splice_Rec_1092821,Human_Splice_Rec_1092943 RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 117231 RMVar_ID_117231 Human_SNP_ID_879262732 m1A Human chr9 + 69035836 69035836 69035836 GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCAGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG GCAGTAGCCGGCCTCCTGGCGTCACCCAGCCCGGCCCAGGCCCAGACCCTCACCCGGGTCCCGCG A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding CDS,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:69035786..69035950 26863196 MeRIP-seq:(Medium) rs2481598 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_5036779 Clinvar_Rec_214 GWAS_ID_7357 117232 RMVar_ID_117232 Human_SNP_ID_879264811 m1A Human chr9 + 134138699 134138699 134138699 GCCACACCTGTTCTCTGCAAAGTGGGTGTTGTAATTTCTCTGCCTTCCTCTTGGATGAAGACTTT GCCACACCTGTTCTCTGCAAAGTGGGTGTTGTTATTTCTCTGCCTTCCTCTTGGATGAAGACTTT A T WDR5 Ensembl:ENSG00000196363 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs35401074 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_3193677,Human_RBP_ID_10422223 117233 RMVar_ID_117233 Human_SNP_ID_879276835 m1A Human chr9 - 134067974 134067974 134067974 GAGCCAAAGAGGAGCCGGCCGCGCGGGCCGGGAGGGGACGGCCGCCGGAGCCGCGAGGCCAAGTA GAGCCAAAGAGGAGCCGGCCGCGCGGGCCGGGGGGGGACGGCCGCCGGAGCCGCGAGGCCAAGTA T C BRD3 Ensembl:ENSG00000169925 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134067883..134068025 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5035973,Human_RBP_ID_9408832,Human_RBP_ID_18427522 Human_Splice_Rec_1096825 117234 RMVar_ID_117234 Human_SNP_ID_879284243 m1A Human chr9 + 134730187 134730187 134730187 CCGGACATGCGGCAAGTCCCAGACCTGGCACCACTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC CCGGACATGCGGCAAGTCCCAGACCTGGCACCGCTGCCGGCCTCCGCCCTGACTCCAGCTGTCTC A G COL5A1 Ensembl:ENSG00000130635 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134730184..134730520 26863196 MeRIP-seq:(Medium) rs3124308 Functional Loss SNV ICGC 33..33 33 COCA 3 - RMVar_hsa_circ_85559,RMVar_hsa_circ_95670,RMVar_hsa_circ_108153,RMVar_hsa_circ_118094,RMVar_hsa_circ_116543,RMVar_hsa_circ_102478,RMVar_hsa_circ_87259,RMVar_hsa_circ_94868,RMVar_hsa_circ_87147,RMVar_hsa_circ_48007,RMVar_hsa_circ_260718,RMVar_hsa_circ_260722,RMVar_hsa_circ_260726,RMVar_hsa_circ_77100,RMVar_hsa_circ_79793,RMVar_hsa_circ_43159,RMVar_hsa_circ_260727,RMVar_hsa_circ_260724,RMVar_hsa_circ_260725,RMVar_hsa_circ_260723,RMVar_hsa_circ_260720,RMVar_hsa_circ_260721,RMVar_hsa_circ_260719,RMVar_hsa_circ_79120,RMVar_hsa_circ_98507,RMVar_hsa_circ_260717,RMVar_hsa_circ_89493,RMVar_hsa_circ_100791,RMVar_hsa_circ_260732,RMVar_hsa_circ_260733,RMVar_hsa_circ_260731,RMVar_hsa_circ_119974,RMVar_hsa_circ_345054,RMVar_hsa_circ_101415,RMVar_hsa_circ_92483,RMVar_hsa_circ_96974,RMVar_hsa_circ_77673,RMVar_hsa_circ_86091,RMVar_hsa_circ_260736,RMVar_hsa_circ_20064,RMVar_hsa_circ_46780,RMVar_hsa_circ_260738,RMVar_hsa_circ_260739,RMVar_hsa_circ_260740,RMVar_hsa_circ_260737,RMVar_hsa_circ_99527,RMVar_hsa_circ_260735,RMVar_hsa_circ_89878,RMVar_hsa_circ_260743,RMVar_hsa_circ_82579,RMVar_hsa_circ_83977,RMVar_hsa_circ_260744,RMVar_hsa_circ_260745,RMVar_hsa_circ_260741,RMVar_hsa_circ_260742 117235 RMVar_ID_117235 Human_SNP_ID_879286122 m1A Human chr9 - 125241293 125241293 125241293 ACAGACAGATTGACCTATTGGGGTGTTTCGCGAGTGTGAGAGGGAAGCGCCGCGGCCTGTATTTC ACAGACAGATTGACCTATTGGGGTGTTTCGCGTGTGTGAGAGGGAAGCGCCGCGGCCTGTATTTC T A HSPA5 Ensembl:ENSG00000044574 Protein coding 5'UTR GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:125240990..125241350 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_92238,Human_RBP_ID_711812,Human_RBP_ID_846483,Human_RBP_ID_1226037,Human_RBP_ID_1702055,Human_RBP_ID_3893278,Human_RBP_ID_5009347,Human_RBP_ID_8696556,Human_RBP_ID_9264664,Human_RBP_ID_9339051,Human_RBP_ID_17715865,Human_RBP_ID_18472789,Human_RBP_ID_22118855,Human_RBP_ID_22466205,Human_RBP_ID_24285635,Human_RBP_ID_27130182 117236 RMVar_ID_117236 Human_SNP_ID_879303030 m1A Human chr9 + 87974498 87974498 87974498 TGTGCCCCTGTGCCCCTGAACTTCCAAACTCCACTTCTCCTCCACCCCACGCTGATCTGAGCTCG TGTGCCCCTGTGCCCCTGAACTTCCAAACTCCCCTTCTCCTCCACCCCACGCTGATCTGAGCTCG A C - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h chr9:87974381..87974716;chr9:87974447..87974694 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 5 ovary 117237 RMVar_ID_117237 Human_SNP_ID_879318729 m1A Human chr9 + 130501033 130501033 130501033 AGCAAGGTCACTGCCAAATAGACCCGTGTACAATGAGGAGCTGGGGCCTCCTCAATTTGCAGATC AGCAAGGTCACTGCCAAATAGACCCGTGTACAGTGAGGAGCTGGGGCCTCCTCAATTTGCAGATC A G ASS1 Ensembl:ENSG00000130707 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:130500967..130501219 26863196 MeRIP-seq:(Medium) rs781440434 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_182974,Human_RBP_ID_17321384 Human_Splice_Rec_1090892,Human_Splice_Rec_1090922,Human_Splice_Rec_1090952,Human_Splice_Rec_1091022 RMVar_hsa_circ_98358,RMVar_hsa_circ_260334 117238 RMVar_ID_117238 Human_SNP_ID_879328260 m1A Human chr9 + 135486833 135486833 135486833 GTCCTGGGAAGAAACCCCCCAGTGTCTTTGGCAGCACGGCAGAGAGGATGAGGCAGGAGGGTGCC GTCCTGGGAAGAAACCCCCCAGTGTCTTTGGCTGCACGGCAGAGAGGATGAGGCAGGAGGGTGCC A T PPP1R26 Ensembl:ENSG00000196422 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:135486782..135486976 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_8926964 RMVar_hsa_circ_113515,RMVar_hsa_circ_260770,RMVar_hsa_circ_123719,RMVar_hsa_circ_260771 117239 RMVar_ID_117239 Human_SNP_ID_879334890 m1A Human chr9 - 96417887 96417887 96417887 CCCGATCAAGCCAACGTGCGGCGGTGGAGGGGAGCCGGAGCCGCCGCCGCCGCTCATCCCCACCA CCCGATCAAGCCAACGTGCGGCGGTGGAGGGGGGCCGGAGCCGCCGCCGCCGCTCATCCCCACCA T C ZNF367 Ensembl:ENSG00000165244 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:96417838..96418291 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_22118751 117240 RMVar_ID_117240 Human_SNP_ID_879341031 m1A Human chr9 + 132944002 132944002 132944002 TCTTTCACCACCAATTAAACACCCACAAGTACACCCAGAGCGAGTCATGCAAATTTCAGCGGAGA TCTTTCACCACCAATTAAACACCCACAAGTACCCCCAGAGCGAGTCATGCAAATTTCAGCGGAGA A C GFI1B Ensembl:ENSG00000165702 Protein coding exon GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:132943995..132944109 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 117241 RMVar_ID_117241 Human_SNP_ID_879360881 m1A Human chr9 - 127872840 127872840 127872840 AATGGGTGGGCGTTTGCAGGTGGGCCTGGCTCAGGGAAGGGCACCCAGTGTGAGAAGATCGTGCA AATGGGTGGGCGTTTGCAGGTGGGCCTGGCTCGGGGAAGGGCACCCAGTGTGAGAAGATCGTGCA T C AL157935.3,AK1 Ensembl:ENSG00000257524,Ensembl:ENSG00000106992 Protein coding,Protein coding 3'UTR,CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:127872676..127872894 26863196 MeRIP-seq:(Medium) rs758239561 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_3974811,Human_RBP_ID_5010408,Human_RBP_ID_9339066,Human_RBP_ID_19025642,Human_RBP_ID_22556228,Human_RBP_ID_22690255 Human_Splice_Rec_1083750,Human_Splice_Rec_1083774,Human_Splice_Rec_1083784,Human_Splice_Rec_1083796,Human_Splice_Rec_1083820,Human_Splice_Rec_1083844,Human_Splice_Rec_1083868,Human_Splice_Rec_1083882,Human_Splice_Rec_1083910,Human_Splice_Rec_1083922,Human_Splice_Rec_1083932 RMVar_hsa_circ_33583 117242 RMVar_ID_117242 Human_SNP_ID_879364930 m1A Human chr9 - 128166205 128166205 128166205 AGCCCCCACTACCTCGGCGCTCAACCCGCCTCAAAACCTGATAGAGGGACCTCCCTGTCCCTGGC AGCCCCCACTACCTCGGCGCTCAACCCGCCTCGAAACCTGATAGAGGGACCTCCCTGTCCCTGGC T C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 11 uterus Human_RBP_ID_712434,Human_RBP_ID_5124191,Human_RBP_ID_27542402 Human_miRNA_ID_2689759,Human_miRNA_ID_2955708 RMVar_hsa_circ_124004,RMVar_hsa_circ_259851 117243 RMVar_ID_117243 Human_SNP_ID_879393677 m1A Human chr9 + 106925553 106925553 106925553 TTGCAGCAGCAACAGCCACCGCAGCCACCACCACCGCCGCCGCCACCACCACCATCACAGCCACA TTGCAGCAGCAACAGCCACCGCAGCCACCACCGCCGCCGCCGCCACCACCACCATCACAGCCACA A G ZNF462 Ensembl:ENSG00000148143 Protein coding intron GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:106925505..106925720 26863196 MeRIP-seq:(Medium) rs146183570 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 4 uterus,large intestine RMVar_hsa_circ_32088,RMVar_hsa_circ_270134,RMVar_hsa_circ_303314,RMVar_hsa_circ_337158,RMVar_hsa_circ_62543,RMVar_hsa_circ_258461,RMVar_hsa_circ_258462 117244 RMVar_ID_117244 Human_SNP_ID_879401100 m1A Human chr9 + 122261504 122261504 122261504 AGTTTTGGTTTCTGCTTCCATCAATGTCTATGAAATACTAAAGGAAATGTGAACATTCAGGCAGG AGTTTTGGTTTCTGCTTCCATCAATGTCTATGCAATACTAAAGGAAATGTGAACATTCAGGCAGG A C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:122261477..122261563 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 117245 RMVar_ID_117245 Human_SNP_ID_879404056 m1A Human chr9 + 128247470 128247470 128247470 CTGGAAGGCCTCCTTCCTGAGGGCTGGCGTGTACCCTGAGCGTGTTGGGGTGAGTGGCAGGGCAA CTGGAAGGCCTCCTTCCTGAGGGCTGGCGTGTTCCCTGAGCGTGTTGGGGTGAGTGGCAGGGCAA A T DNM1 Ensembl:ENSG00000106976 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:128247395..128247932 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 11 lung Human_RBP_ID_3975824,Human_RBP_ID_18172965,Human_RBP_ID_22484374,Human_RBP_ID_26362152,Human_RBP_ID_27832753 Human_Splice_Rec_1085186,Human_Splice_Rec_1085187,Human_Splice_Rec_1085228,Human_Splice_Rec_1085229,Human_Splice_Rec_1085268,Human_Splice_Rec_1085269,Human_Splice_Rec_1085310,Human_Splice_Rec_1085311,Human_Splice_Rec_1085350,Human_Splice_Rec_1085351,Human_Splice_Rec_1085408,Human_Splice_Rec_1085409,Human_Splice_Rec_1085448,Human_Splice_Rec_1085449,Human_Splice_Rec_1085488,Human_Splice_Rec_1085489,Human_Splice_Rec_1085528,Human_Splice_Rec_1085529,Human_Splice_Rec_1085586,Human_Splice_Rec_1085587,Human_Splice_Rec_1085634,Human_Splice_Rec_1085642 RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259866,RMVar_hsa_circ_266850,RMVar_hsa_circ_51735,RMVar_hsa_circ_12650,RMVar_hsa_circ_50406 117246 RMVar_ID_117246 Human_SNP_ID_879407185 m1A Human chr9 + 111896852 111896840 111896852 CGGAGCTGCGGCGGTGGAGCTGCTCGGCCGGGAGCCCGGCGGCGAGACGGAGAGGCGGCGGAGGT CGGAGCTGCGGCGGTGGAGCT____________GCCCGGCGGCGAGACGGAGAGGCGGCGGAGGT TGCTCGGCCGGGA T UGCG Ensembl:ENSG00000148154 Protein coding 5'UTR GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:111896800..111897270 26863196 MeRIP-seq:(Medium) rs1309149829 Functional Loss DEL ICGC 22..33 33 PBCA 1 - Human_RBP_ID_5006194,Human_RBP_ID_18427785,Human_RBP_ID_22467378 117247 RMVar_ID_117247 Human_SNP_ID_879412764 m1A Human chr9 + 93527172 93527172 93527172 TCATTTTATGTTTAGCCATATCAGCGGGAACAAGATTGGCTGGGAGAAGACGGGAAGCCACTCAG TCATTTTATGTTTAGCCATATCAGCGGGAACAGGATTGGCTGGGAGAAGACGGGAAGCCACTCAG A G FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:93516147..93527182 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_3974606,Human_RBP_ID_5226676,Human_RBP_ID_16742198,Human_RBP_ID_22691202,Human_RBP_ID_26360836 Human_Splice_Rec_1062650,Human_Splice_Rec_1062651,Human_Splice_Rec_1062684,Human_Splice_Rec_1062685,Human_Splice_Rec_1062700,Human_Splice_Rec_1062701 RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_302669,RMVar_hsa_circ_341422,RMVar_hsa_circ_357743,RMVar_hsa_circ_293842,RMVar_hsa_circ_119641,RMVar_hsa_circ_257868,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257869,RMVar_hsa_circ_257866,RMVar_hsa_circ_257867,RMVar_hsa_circ_257865,RMVar_hsa_circ_257863,RMVar_hsa_circ_372636,RMVar_hsa_circ_95302,RMVar_hsa_circ_77870,RMVar_hsa_circ_257879,RMVar_hsa_circ_257877,RMVar_hsa_circ_257878,RMVar_hsa_circ_374941,RMVar_hsa_circ_116385,RMVar_hsa_circ_29491,RMVar_hsa_circ_76732,RMVar_hsa_circ_317606,RMVar_hsa_circ_257886,RMVar_hsa_circ_257887,RMVar_hsa_circ_350096,RMVar_hsa_circ_354330,RMVar_hsa_circ_266951,RMVar_hsa_circ_118728,RMVar_hsa_circ_257888,RMVar_hsa_circ_257890,RMVar_hsa_circ_257889,RMVar_hsa_circ_100907,RMVar_hsa_circ_257893,RMVar_hsa_circ_257896,RMVar_hsa_circ_306542,RMVar_hsa_circ_309814,RMVar_hsa_circ_302985,RMVar_hsa_circ_257895 117248 RMVar_ID_117248 Human_SNP_ID_879431925 m1A Human chr9 + 87497978 87497978 87497978 CGCAGCGGCAGGGTCTGGGGCCGGCGCCTGGGAGGGATCTGCGCCCCCCACTCACTCCCTAGCTG CGCAGCGGCAGGGTCTGGGGCCGGCGCCTGGGGGGGATCTGCGCCCCCCACTCACTCCCTAGCTG A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:87497953..87498104 26863196 MeRIP-seq:(Medium) rs2302791 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5035736,Human_RBP_ID_9408139,Human_RBP_ID_18427169 117249 RMVar_ID_117249 Human_SNP_ID_879436868 m1A Human chr9 - 133057941 133057941 133057941 TAGTCCAGAATCTCTGTCTCCATTTCGTTTTCACTGCCGTCGGATGGCTTGAAGTCCTCCTCCTC TAGTCCAGAATCTCTGTCTCCATTTCGTTTTCGCTGCCGTCGGATGGCTTGAAGTCCTCCTCCTC T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated chr9:133057801..133058052;chr9:133057826..133058007 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 6 lung 117250 RMVar_ID_117250 Human_SNP_ID_879472648 m1A Human chr9 - 124414904 124414904 124414904 GGAATGCCGTCTTGGAAGCCGATTTTGCAAAGAGGGGATACAAGCTTCCAAAGGTCCGGAAAACT GGAATGCCGTCTTGGAAGCCGATTTTGCAAAGTGGGGATACAAGCTTCCAAAGGTCCGGAAAACT T A PSMB7 Ensembl:ENSG00000136930 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_91215,Human_RBP_ID_5036386,Human_RBP_ID_5329605,Human_RBP_ID_9339042,Human_RBP_ID_18140621,Human_RBP_ID_22467052,Human_RBP_ID_24284675 Human_Splice_Rec_1079314,Human_Splice_Rec_1079315,Human_Splice_Rec_1079328,Human_Splice_Rec_1079329,Human_Splice_Rec_1079346,Human_Splice_Rec_1079347,Human_Splice_Rec_1079357 RMVar_hsa_circ_19035,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52664,RMVar_hsa_circ_333929,RMVar_hsa_circ_259465,RMVar_hsa_circ_259463,RMVar_hsa_circ_92482 117251 RMVar_ID_117251 Human_SNP_ID_879483347 m1A Human chr9 - 35685668 35685668 35685668 TACAGCCCTGCAGAAGCTGGAGGAGGCCGAGAAGGCGGCTGATGAGAGCGAGAGGTGGTCAGGGG TACAGCCCTGCAGAAGCTGGAGGAGGCCGAGACGGCGGCTGATGAGAGCGAGAGGTGGTCAGGGG T G TPM2 Ensembl:ENSG00000198467 Protein coding CDS GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:35685251..35685750 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 12 caecum,large intestine Human_Splice_Rec_1042257,Human_Splice_Rec_1042273,Human_Splice_Rec_1042287,Human_Splice_Rec_1042303,Human_Splice_Rec_1042319,Human_Splice_Rec_1042343,Human_Splice_Rec_1042354,Human_Splice_Rec_1042355 Human_miRNA_ID_3010528 RMVar_hsa_circ_106733,RMVar_hsa_circ_256626,RMVar_hsa_circ_80855,RMVar_hsa_circ_256628 117252 RMVar_ID_117252 Human_SNP_ID_879490833 m1A Human chr9 + 136719718 136719718 136719718 TGGTAGGTGCCCAGGACCATGGAGGCAGCTCCATCTCCCCACCCCTGGGGGACCCTGGAGCCCCA TGGTAGGTGCCCAGGACCATGGAGGCAGCTCCGTCTCCCCACCCCTGGGGGACCCTGGAGCCCCA A G DIPK1B Ensembl:ENSG00000165716 Protein coding intron GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs9411219 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 1 brain Human_RBP_ID_8159855,Human_RBP_ID_27133553 117253 RMVar_ID_117253 Human_SNP_ID_879506663 m1A Human chr9 - 129176996 129176996 129176996 TCTGCCCGGACTCGTCCCCGGACGCGTCCAACATCTCAAACTTGATCTCCATCTTTGGCTCCGGC TCTGCCCGGACTCGTCCCCGGACGCGTCCAACTTCTCAAACTTGATCTCCATCTTTGGCTCCGGC T A IER5L Ensembl:ENSG00000188483 Protein coding CDS GSE70485:GSM1782896,GSM1782897 HEPG2 cell line,total RNA Untreated, competitive elution chr9:129176951..129177000 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 adrenal_gland non_functioning 1 kidney Human_RBP_ID_27542779 117254 RMVar_ID_117254 Human_SNP_ID_879537004 m1A Human chr9 + 128656593 128656593 128656593 GGACGGCCCTCCACTGCGAGGGCACGGACGCCACACCCAGGGTCTCGTCCTGCAGCGGCCCTGGC GGACGGCCCTCCACTGCGAGGGCACGGACGCCGCACCCAGGGTCTCGTCCTGCAGCGGCCCTGGC A G - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:128640694..128656689 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 117255 RMVar_ID_117255 Human_SNP_ID_879546498 m1A Human chr9 - 21994234 21994234 21994234 TTTCGTGGTTCACATCCCGCGGCTCACGGGGGAGTGGGCAGCGCCAGGGGCGCCCGCCGCTGTGG TTTCGTGGTTCACATCCCGCGGCTCACGGGGGTGTGGGCAGCGCCAGGGGCGCCCGCCGCTGTGG T A CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_92524,Human_RBP_ID_256694,Human_RBP_ID_717061,Human_RBP_ID_5024706,Human_RBP_ID_22339396,Human_RBP_ID_22838468,Human_RBP_ID_24523189 Human_Splice_Rec_1035553,Human_Splice_Rec_1035563 117256 RMVar_ID_117256 Human_SNP_ID_879546509 m1A Human chr9 - 21994234 21994234 21994234 TTTCGTGGTTCACATCCCGCGGCTCACGGGGGAGTGGGCAGCGCCAGGGGCGCCCGCCGCTGTGG TTTCGTGGTTCACATCCCGCGGCTCACGGGGGGGTGGGCAGCGCCAGGGGCGCCCGCCGCTGTGG T C CDKN2A Ensembl:ENSG00000147889 Protein coding CDS GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_92524,Human_RBP_ID_256694,Human_RBP_ID_717061,Human_RBP_ID_5024706,Human_RBP_ID_22339396,Human_RBP_ID_22838468,Human_RBP_ID_24523189 Human_Splice_Rec_1035553,Human_Splice_Rec_1035563 117257 RMVar_ID_117257 Human_SNP_ID_879555588 m1A Human chr9 - 128626510 128626510 128626510 GAGGAGCGGAAGGCGTCGTGGGCCTCGCGCAAAGCTTTGATTTCTTCCAAGGAGTTGCAGCGCAC GAGGAGCGGAAGGCGTCGTGGGCCTCGCGCAACGCTTTGATTTCTTCCAAGGAGTTGCAGCGCAC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1782892,GSM1782893;GSE70485:GSM1782896,GSM1782897;GSE70485:GSM1972533,GSM1972534 HeLa cell line,mRNA;HEPG2 cell line,total RNA rearranged at 50c;HEPG2 cell line,total RNA Untreated, competitive elution;HEPG2 cell line,total RNA Untreated chr9:128626376..128626723;chr9:128626357..128626700;chr9:128626346..128626675;chr9:128626451..128626600 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 7 uterus 117258 RMVar_ID_117258 Human_SNP_ID_879557300 m1A Human chr9 + 37588920 37588920 37588920 TGTCCTGTCTTCATATGCTGTCCAATTTCTTTAAGATAAATGGAGCTGAAAGAAAAACAAATCTA TGTCCTGTCTTCATATGCTGTCCAATTTCTTTGAGATAAATGGAGCTGAAAGAAAAACAAATCTA A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:37588801..37592343 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung 117259 RMVar_ID_117259 Human_SNP_ID_879558197 m1A Human chr9 + 21971204 21971204 21971204 GCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGC GCAGCTCCGCCACTCGGGCGCTGCCCATCATCTTGACCTGCCAGAGAGAACAGAATGGTCAGAGC A T AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21970862..21971254 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma,oesophagus squamous_cell_carcinoma 20 pancreas,oesophagus 117260 RMVar_ID_117260 Human_SNP_ID_879558274 m1A Human chr9 + 21971204 21971204 21971204 GCAGCTCCGCCACTCGGGCGCTGCCCATCATCATGACCTGCCAGAGAGAACAGAATGGTCAGAGC GCAGCTCCGCCACTCGGGCGCTGCCCATCATCCTGACCTGCCAGAGAGAACAGAATGGTCAGAGC A C AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:21970862..21971254 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 ovary mucinous_carcinoma,lung adenocarcinoma,LUAD 22 lung,ovary 117261 RMVar_ID_117261 Human_SNP_ID_879571793 m1A Human chr9 - 13119578 13119578 13119578 AGGAATTGCAGATGCCGATGGAAGACTGATGCAGGGAGACCAGATATTAATGGTGAATGGGGAAG AGGAATTGCAGATGCCGATGGAAGACTGATGCGGGGAGACCAGATATTAATGGTGAATGGGGAAG T C MPDZ Ensembl:ENSG00000107186 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:13109023..13119701 32194978 MeRIP-seq:(Medium) rs779043354 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_1031810,Human_Splice_Rec_1031811,Human_Splice_Rec_1031827,Human_Splice_Rec_1031914,Human_Splice_Rec_1031915,Human_Splice_Rec_1032002,Human_Splice_Rec_1032003,Human_Splice_Rec_1032058,Human_Splice_Rec_1032059,Human_Splice_Rec_1032088,Human_Splice_Rec_1032089,Human_Splice_Rec_1032130,Human_Splice_Rec_1032131,Human_Splice_Rec_1032178,Human_Splice_Rec_1032179,Human_Splice_Rec_1032226,Human_Splice_Rec_1032227,Human_Splice_Rec_1032314,Human_Splice_Rec_1032315,Human_Splice_Rec_1032400,Human_Splice_Rec_1032401,Human_Splice_Rec_1032438,Human_Splice_Rec_1032439,Human_Splice_Rec_1032532,Human_Splice_Rec_1032533,Human_Splice_Rec_1032554,Human_Splice_Rec_1032555 RMVar_hsa_circ_52340,RMVar_hsa_circ_63884,RMVar_hsa_circ_69191,RMVar_hsa_circ_74184 117262 RMVar_ID_117262 Human_SNP_ID_879581479 m1A Human chr9 - 134691020 134691020 134691020 TGAGCTGCGCGTCTTTGGTGACTCTGTAAGCGACATCCGGGCCTTTGGAAGATCGCCGCGTGGCG TGAGCTGCGCGTCTTTGGTGACTCTGTAAGCGGCATCCGGGCCTTTGGAAGATCGCCGCGTGGCG T C - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:134690862..134691107 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 117263 RMVar_ID_117263 Human_SNP_ID_879589922 m1A Human chr9 + 120531111 120531111 120531111 TAGGGCCTACCAGATCAGAGGGCCCTGCCGACAGCTTCAGTCTCATCTCTCACGGGAAACCATCA TAGGGCCTACCAGATCAGAGGGCCCTGCCGACGGCTTCAGTCTCATCTCTCACGGGAAACCATCA A G - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:120531109..120531213 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 117264 RMVar_ID_117264 Human_SNP_ID_879607250 m1A Human chr9 - 20622391 20622391 20622391 GCGAGCAAGCGAGCGCGGGGGGAAAAAGGCAGAGAATGTCCGCCATCTACCCTCCGCTCCTGGGC GCGAGCAAGCGAGCGCGGGGGGAAAAAGGCAGCGAATGTCCGCCATCTACCCTCCGCTCCTGGGC T G MLLT3 Ensembl:ENSG00000171843 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:20622340..20622493 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_22838442,Human_RBP_ID_23091766,Human_RBP_ID_26242719 117265 RMVar_ID_117265 Human_SNP_ID_879610022 m1A Human chr9 + 129719279 129719279 129719279 GGGGCGCGGTAGCGCCGCCAAGCGGAAGAAGAAGCAGCGGCGGAACCGCACCACGTTCAACAGCA GGGGCGCGGTAGCGCCGCCAAGCGGAAGAAGACGCAGCGGCGGAACCGCACCACGTTCAACAGCA A C PRRX2 Ensembl:ENSG00000167157 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:129719204..129719289 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 2 liver Human_Splice_Rec_1089890 RMVar_hsa_circ_298776 117266 RMVar_ID_117266 Human_SNP_ID_879617587 m1A Human chr9 + 130172676 130172676 130172676 GGGGGCCGCGGCCGCCGAGGATGGGGAAATCCAACAGCAAGTTGAAGCCCGAAGTTGTGGAGGAG GGGGGCCGCGGCCGCCGAGGATGGGGAAATCCGACAGCAAGTTGAAGCCCGAAGTTGTGGAGGAG A G NCS1 Ensembl:ENSG00000107130 Protein coding CDS GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:130172501..130172767 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 2 liver Human_Splice_Rec_1090543 117267 RMVar_ID_117267 Human_SNP_ID_879638399 m1A Human chr9 + 120409133 120409133 120409133 GGCCACCAGGGAAGCACAGCCACTACCTGCTCAGCTCCTGGCCGCTGCAGCGGACCTCCTGGATC GGCCACCAGGGAAGCACAGCCACTACCTGCTCGGCTCCTGGCCGCTGCAGCGGACCTCCTGGATC A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:120409126..120409250 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach 117268 RMVar_ID_117268 Human_SNP_ID_879640326 m1A Human chr9 + 32451146 32451146 32451146 CCAATTATCTGCTCATTTTTACCCCTGTAGTCATTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC CCAATTATCTGCTCATTTTTACCCCTGTAGTCGTTTCTGGGCATGCCTTAGTTTGCTTGGGTTGC A G ACO1 Ensembl:ENSG00000122729 Protein coding 3'UTR GSM3896225,GSM3896226,GSM3896227,GSM3896228,GSM3896229,GSM3896230 HEK-293T cells,m1A-quant-seq - 31548705 m1A-quant-seq:(High) rs7042042 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver Human_RBP_ID_26564989 GWAS_ID_7845,GWAS_ID_7846,GWAS_ID_7847,GWAS_ID_7848,GWAS_ID_7849,GWAS_ID_7850,GWAS_ID_7851,GWAS_ID_7852 117269 RMVar_ID_117269 Human_SNP_ID_879675994 m1A Human chr9 - 137834392 137834392 137834392 TGGGCTCGCAGTGGTGGTTGATGAACCGGCTGACGTTCCCGTAGAACCGCGCGTCGATGCAGTAA TGGGCTCGCAGTGGTGGTTGATGAACCGGCTGGCGTTCCCGTAGAACCGCGCGTCGATGCAGTAA T C - - Other Unknown GSE70485:GSM1782892,GSM1782893 HEPG2 cell line,total RNA rearranged at 50c chr9:137834296..137834475 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,COSMIC 33..33 33 STAD,stomach adenocarcinoma 3 stomach 117270 RMVar_ID_117270 Human_SNP_ID_879677269 m1A Human chr9 + 20414312 20414312 20414312 CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT CTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT A G - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:20414265..20448222 26863196 MeRIP-seq:(Medium) rs148318848 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm,central_nervous_system astrocytoma_Grade_IV,caecum adenocarcinoma,brain astrocytoma_Grade_IV,large_intestine adenocarcinoma 9 caecum,head and neck,large intestine,brain 117271 RMVar_ID_117271 Human_SNP_ID_879684091 m1A Human chr9 - 87148861 87148861 87148861 TTTTTCCATTTGCACCGACTGAGCAGGAGGCCAGGCCTCCCCGCCCGGGCCTTGCGAGCGAGGCC TTTTTCCATTTGCACCGACTGAGCAGGAGGCCTGGCCTCCCCGCCCGGGCCTTGCGAGCGAGGCC T A - - Other Unknown GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:87148814..87148918 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 117272 RMVar_ID_117272 Human_SNP_ID_879689244 m1A Human chr9 + 21968239 21968239 21968239 TCTCAGAGCCTCTCTGGTTCTTTCAATCGGGGATGTCTGCAGAGGGCAGAAAGAAAACAGGCGTT TCTCAGAGCCTCTCTGGTTCTTTCAATCGGGGGTGTCTGCAGAGGGCAGAAAGAAAACAGGCGTT A G AL359922.1 Ensembl:ENSG00000264545 Protein coding intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891;GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530;GSE70485:GSM1972531,GSM1972532;GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HeLa cell line,mRNA;HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h;HEPG2 cell line,mRNA heat shock 4h;HTR8/Svneo,Hypoxia IP chr9:21968078..21968285;chr9:21968026..21968267;chr9:21968026..21968280;chr9:21968026..21968289;chr9:21968151..21968250 26863196,32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue myelodysplastic_syndrome 8 haematopoietic and lymphoid tissue 117273 RMVar_ID_117273 Human_SNP_ID_879698549 m1A Human chr9 + 129110696 129110696 129110696 GCGCCCACCCTCTGGGCCGAGCGGGCTGCGGGAAGGCACCCGGGGAGGAGGACTCGCGAGGCGGG GCGCCCACCCTCTGGGCCGAGCGGGCTGCGGGCAGGCACCCGGGGAGGAGGACTCGCGAGGCGGG A C - - Other Unknown GSE73941:GSM1906567,GSM1906568,GSM1906569,GSM1906570 HEK293T,ALKBH3 KO chr9:129110601..129110775 26863410 MeRIP-seq:(Medium) rs3118624 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 2 brain GWAS_ID_14738 117274 RMVar_ID_117274 Human_SNP_ID_879720903 m1A Human chr9 - 136669993 136669993 136669993 GTAGAGCCAGCCTCACCTGACTGGCAAGTGTCACCCCGCCATCCTGCAGGGCAGCGGCAGCGGCC GTAGAGCCAGCCTCACCTGACTGGCAAGTGTCCCCCCGCCATCCTGCAGGGCAGCGGCAGCGGCC T G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:136669583..136670035 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 breast HER-positive_carcinoma 4 breast 117275 RMVar_ID_117275 Human_SNP_ID_879738555 m1A Human chr9 + 97412214 97412214 97412214 CGGCGGCAGGAGCTGGGCCCAGAGACGCGGGGACGGGCCGTGGGCCCCCGGAACGAGGTGAGTGC CGGCGGCAGGAGCTGGGCCCAGAGACGCGGGGGCGGGCCGTGGGCCCCCGGAACGAGGTGAGTGC A G TDRD7 Ensembl:ENSG00000196116 Protein coding 5'UTR GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:97412163..97412263 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_19023988 Human_Splice_Rec_1066209 117276 RMVar_ID_117276 Human_SNP_ID_879750705 m1A Human chr9 - 136451298 136451298 136451298 CTGTCTCTCTCACCCGCTCCCGAAACAAAGAGACCCGGACAGGCAGCCAAGAAAGAAACGAAGGA CTGTCTCTCTCACCCGCTCCCGAAACAAAGAGGCCCGGACAGGCAGCCAAGAAAGAAACGAAGGA T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE70485:GSM1972533,GSM1972534 HEPG2 cell line,total RNA Untreated chr9:136451251..136451425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 COAD 1 - Human_RBP_ID_27544242 Human_Splice_Rec_1099655,Human_Splice_Rec_1099715,Human_Splice_Rec_1099751,Human_Splice_Rec_1099803,Human_Splice_Rec_1099859,Human_Splice_Rec_1099931 RMVar_hsa_circ_10442,RMVar_hsa_circ_46101,RMVar_hsa_circ_308925,RMVar_hsa_circ_91777,RMVar_hsa_circ_269804,RMVar_hsa_circ_54571,RMVar_hsa_circ_42427,RMVar_hsa_circ_260868,RMVar_hsa_circ_61233 117277 RMVar_ID_117277 Human_SNP_ID_879753242 m1A Human chr9 - 128424510 128424510 128424510 AGAAAGCAAGCTGGTCTGCCCCTTCAGCCCGCAGGGATGCAAGGAAGGTGGAGTGGACCATGGGG AGAAAGCAAGCTGGTCTGCCCCTTCAGCCCGCTGGGATGCAAGGAAGGTGGAGTGGACCATGGGG T A RF00017-1784,RF00017-4503 RNACentral:URS0000904F64,RNACentral:URS0000948B80 SRP RNA,SRP RNA intron,intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:128424461..128424554 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver 117278 RMVar_ID_117278 Human_SNP_ID_879767790 m1A Human chr9 + 35717760 35717760 35717760 TTGAGGACCAGGGCAGCTGCAGCACTTGCCACAGCTTTGGCGAGCTGCATTAGCGCATCCTGTGA TTGAGGACCAGGGCAGCTGCAGCACTTGCCACGGCTTTGGCGAGCTGCATTAGCGCATCCTGTGA A G - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:35717601..35717800 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 117279 RMVar_ID_117279 Human_SNP_ID_879802785 m1A Human chr9 + 127502886 127502886 127502886 CCGCCAGGACATCGCCCAGCGCCTCCGCATCTACCACAGCAGCTGAGTGCTGCCCGCCCACCTGG CCGCCAGGACATCGCCCAGCGCCTCCGCATCTGCCACAGCAGCTGAGTGCTGCCCGCCCACCTGG A G LRSAM1 Ensembl:ENSG00000148356 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127502835..127502965 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 6 stomach 117280 RMVar_ID_117280 Human_SNP_ID_879816441 m1A Human chr9 - 133363504 133363501 133363504 GCCCTGGGGGTGTCTCCATGGATGAGAAGAAGAAGGAGTGGTAACAGTCACAGATCCCTACCTGC GCCCTGGGGGTGTCTCCATGGATGAGAAGAAG___GAGTGGTAACAGTCACAGATCCCTACCTGC CCTT C SURF4 Ensembl:ENSG00000148248 Protein coding 3'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:133363228..133363601 26863196 MeRIP-seq:(Medium) rs782142213 Functional Loss DEL TCGA 33..35 33 PRAD,LGG 2 - Human_RBP_ID_714357,Human_RBP_ID_2062023,Human_RBP_ID_5017504,Human_RBP_ID_7906822,Human_RBP_ID_16611363,Human_RBP_ID_18905604,Human_RBP_ID_22466647,Human_RBP_ID_22777104,Human_RBP_ID_24291294 Human_miRNA_ID_2037162,Human_miRNA_ID_2347864,Human_miRNA_ID_2708488 RMVar_hsa_circ_86369,RMVar_hsa_circ_109052,RMVar_hsa_circ_260652,RMVar_hsa_circ_260653 117281 RMVar_ID_117281 Human_SNP_ID_879825667 m1A Human chr9 + 137582472 137582472 137582472 CGCAGCTGGCTTTTTTGGCACCTCCAGGTTCAACCACCAGTCTGTCTCTGCTGTGCCCAGGGTAG CGCAGCTGGCTTTTTTGGCACCTCCAGGTTCAGCCACCAGTCTGTCTCTGCTGTGCCCAGGGTAG A G - - Other Unknown GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137582421..137582637 26863196 MeRIP-seq:(Medium) rs1255623461 Functional Loss SNV TCGA,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 2 uterus 117282 RMVar_ID_117282 Human_SNP_ID_879841738 m1A Human chr9 + 127451368 127451368 127451368 CGGATGAACCCGGATTCGGGACGACCGAAGGAAGTTGCACCTTGGCCTCCTCCGAGCCGAAAGCC CGGATGAACCCGGATTCGGGACGACCGAAGGACGTTGCACCTTGGCCTCCTCCGAGCCGAAAGCC A C RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:127451174..127451384 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 4 kidney 117283 RMVar_ID_117283 Human_SNP_ID_879849910 m1A Human chr9 + 12775745 12775745 12775745 GTCATGGAAGACAGCCCGCTGCCAGACCTCAGAGACATCGAGCTGAAGCTGGGGCGCAAAGTACC GTCATGGAAGACAGCCCGCTGCCAGACCTCAGGGACATCGAGCTGAAGCTGGGGCGCAAAGTACC A G LURAP1L Ensembl:ENSG00000153714 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:12775653..12775927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 117284 RMVar_ID_117284 Human_SNP_ID_879849997 m1A Human chr9 + 12775745 12775745 12775745 GTCATGGAAGACAGCCCGCTGCCAGACCTCAGAGACATCGAGCTGAAGCTGGGGCGCAAAGTACC GTCATGGAAGACAGCCCGCTGCCAGACCTCAGTGACATCGAGCTGAAGCTGGGGCGCAAAGTACC A T LURAP1L Ensembl:ENSG00000153714 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:12775653..12775927 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - 117285 RMVar_ID_117285 Human_SNP_ID_879850881 m1A Human chr9 + 120905206 120905206 120905206 AGGTCAGGCCGGAAGGCGTCAATGGCGTGCTCACGGTTGTTCTGGTCCAGCAGCATGAAGGTGAC AGGTCAGGCCGGAAGGCGTCAATGGCGTGCTCGCGGTTGTTCTGGTCCAGCAGCATGAAGGTGAC A G - - Other Unknown GSE73941:GSM1906561,GSM1906562,GSM1906563,GSM1906564 HEK293T,Wild Type chr9:120905122..120905209 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine 117286 RMVar_ID_117286 Human_SNP_ID_879889877 m1A Human chr9 + 74952316 74952316 74952316 CCCCCGGCCCCGGCAGTACGGGCGGCGGCGGCAGCGGCGGATCGCCTGTCTCCAGACCGTGGTCC CCCCCGGCCCCGGCAGTACGGGCGGCGGCGGCGGCGGCGGATCGCCTGTCTCCAGACCGTGGTCC A G - - Other Unknown GSE73941:GSM1906581,GSM1906582,GSM1906583,GSM1906584 HEK293T,untreat control chr9:74952245..74952327 26863410 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 COAD 1 - 117287 RMVar_ID_117287 Human_SNP_ID_879890088 m1A Human chr9 - 137018300 137018300 137018300 GAAGGACGGCTCGCTCCCGCCTCACGTGCACTACAAGATCCGCCAGAACTCCAGCTTCACCGAGA GAAGGACGGCTCGCTCCCGCCTCACGTGCACTGCAAGATCCGCCAGAACTCCAGCTTCACCGAGA T C ABCA2 Ensembl:ENSG00000107331 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:137018177..137018425 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_3976227,Human_RBP_ID_9408969,Human_RBP_ID_21702885,Human_RBP_ID_22628951 Human_Splice_Rec_1101574,Human_Splice_Rec_1101666,Human_Splice_Rec_1101760,Human_Splice_Rec_1101852,Human_Splice_Rec_1102014,Human_Splice_Rec_1102106,Human_Splice_Rec_1102282 RMVar_hsa_circ_101033,RMVar_hsa_circ_260961 117288 RMVar_ID_117288 Human_SNP_ID_879892800 m1A Human chr9 + 25677561 25677561 25677561 CCGGAAGTGTCCACTGGTGGGGGCGGGAAGGCACCGTAGTCCAAGGTATCCGCGGGCAGGGAGCG CCGGAAGTGTCCACTGGTGGGGGCGGGAAGGCTCCGTAGTCCAAGGTATCCGCGGGCAGGGAGCG A T - - Other Unknown GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:25677511..25677805 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 117289 RMVar_ID_117289 Human_SNP_ID_879907511 m1A Human chr9 - 137517273 137517273 137517273 GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGAGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT GGATGGAGTGGACAGAGTGGAGTGAGTGAGTGTGGGATGGAGTGGACAGAGTGGAGTGAGTGAGT T A PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA heat shock 4h chr9:137517222..137517410;chr9:137516961..137517572 26863196 MeRIP-seq:(Medium) rs377731762 Functional Loss SNV COSMIC 33..33 33 liver neoplasm 2 liver Human_RBP_ID_24293485 RMVar_hsa_circ_55214 117290 RMVar_ID_117290 Human_SNP_ID_879912323 m1A Human chr9 + 2834075 2834075 2834075 TCCCACATCTGCTTTGCCCGAACAACAATGTCATAGTTGGTTTTATCACTGAGTTGTCTGCTTTG TCCCACATCTGCTTTGCCCGAACAACAATGTCTTAGTTGGTTTTATCACTGAGTTGTCTGCTTTG A T - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:2833389..2834136 32194978 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 117291 RMVar_ID_117291 Human_SNP_ID_879916196 m1A Human chr9 + 135485477 135485477 135485477 CGCAGGAGAACGAGGGCAGCACGAAGCCGGCAACCCCCTGCCGCCCTTCAGAAGCAGCACAGAAT CGCAGGAGAACGAGGGCAGCACGAAGCCGGCATCCCCCTGCCGCCCTTCAGAAGCAGCACAGAAT A T PPP1R26 Ensembl:ENSG00000196422 Protein coding CDS GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:135485430..135485763 26863196 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic 5 skin Human_RBP_ID_5535202 RMVar_hsa_circ_113515,RMVar_hsa_circ_260770,RMVar_hsa_circ_123719,RMVar_hsa_circ_260771 117292 RMVar_ID_117292 Human_SNP_ID_879917624 m1A Human chr9 + 6413501 6413501 6413501 CGGTTCCTCTCTAGGCGCCAAGATGTGGATACAGGTTCGCACCATTGATGGCTCCAAGACGTGCA CGGTTCCTCTCTAGGCGCCAAGATGTGGATACGGGTTCGCACCATTGATGGCTCCAAGACGTGCA A G UHRF2 Ensembl:ENSG00000147854 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:6413451..6413525 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 GBM,central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 4 brain Human_RBP_ID_719641,Human_RBP_ID_1705589,Human_RBP_ID_9314948,Human_RBP_ID_9407916,Human_RBP_ID_16687512 Human_Splice_Rec_1030138 RMVar_hsa_circ_123875,RMVar_hsa_circ_255540 117293 RMVar_ID_117293 Human_SNP_ID_879917937 m1A Human chr9 + 111370627 111370627 111370627 GGTTGATTGGGCACAGACTTTTCCAGCTCTGCACTACAGGGTCCATACAAAAGCATCAGAAGTTA GGTTGATTGGGCACAGACTTTTCCAGCTCTGCGCTACAGGGTCCATACAAAAGCATCAGAAGTTA A G - - Other Unknown GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:111370576..111372463 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus 117294 RMVar_ID_117294 Human_SNP_ID_879934988 m1A Human chr9 + 33265077 33265077 33265077 CTCTAGTGTTTGGGTTTCTTCGCGGCTGCTCAAGATGAACCGACTCTTCGGGAAAGCGAAACCCA CTCTAGTGTTTGGGTTTCTTCGCGGCTGCTCATGATGAACCGACTCTTCGGGAAAGCGAAACCCA A T CHMP5 Ensembl:ENSG00000086065 Protein coding 5'UTR GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:33265027..33265149 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach Human_RBP_ID_962495,Human_RBP_ID_1704833,Human_RBP_ID_5329452,Human_RBP_ID_5431162,Human_RBP_ID_5482050,Human_RBP_ID_5516068,Human_RBP_ID_9406850,Human_RBP_ID_22339654,Human_RBP_ID_22466046,Human_RBP_ID_27545528 Human_Splice_Rec_1038099,Human_Splice_Rec_1038111 117295 RMVar_ID_117295 Human_SNP_ID_879954875 m1A Human chr9 + 114289276 114289276 114289276 GCATCCGGGACCCCGGGGGTGGCCGGGACCCAAAGGATCGAAAGGCGCAGAGGTAAGAGGGCCGG GCATCCGGGACCCCGGGGGTGGCCGGGACCCAGAGGATCGAAAGGCGCAGAGGTAAGAGGGCCGG A G COL27A1 Ensembl:ENSG00000196739 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:114282525..114290253 32194978 MeRIP-seq:(Medium) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_847800,Human_RBP_ID_963629,Human_RBP_ID_9408390,Human_RBP_ID_19024222,Human_RBP_ID_22748017,Human_RBP_ID_23094811 Human_Splice_Rec_1073964,Human_Splice_Rec_1073965,Human_Splice_Rec_1074092,Human_Splice_Rec_1074093 RMVar_hsa_circ_79983,RMVar_hsa_circ_258939,RMVar_hsa_circ_109166,RMVar_hsa_circ_258941 117296 RMVar_ID_117296 Human_SNP_ID_879959156 m1A Human chr9 + 136670956 136670956 136670956 GACCCAGCGCCTGGCTCTGCCCGCAGGAGTGGACAGTGCAATGAAGGAAGAAGTGCAGAGGCTGC GACCCAGCGCCTGGCTCTGCCCGCAGGAGTGGGCAGTGCAATGAAGGAAGAAGTGCAGAGGCTGC A G EGFL7 Ensembl:ENSG00000172889 Protein coding CDS GSE135403:GSM4007704,GSM4007705,GSM4007706,GSM4007707 HTR8/Svneo,Hypoxia IP chr9:136670951..136671025 32194978 MeRIP-seq:(Medium) rs746198843 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 4 kidney Human_RBP_ID_961851,Human_RBP_ID_3975180,Human_RBP_ID_5228180,Human_RBP_ID_5329789,Human_RBP_ID_8944752,Human_RBP_ID_9339735,Human_RBP_ID_9341812,Human_RBP_ID_21996318,Human_RBP_ID_22630231,Human_RBP_ID_22690620,Human_RBP_ID_22748360,Human_RBP_ID_23216600,Human_RBP_ID_26361474 Human_Splice_Rec_1100086,Human_Splice_Rec_1100087,Human_Splice_Rec_1100106,Human_Splice_Rec_1100107,Human_Splice_Rec_1100124,Human_Splice_Rec_1100125,Human_Splice_Rec_1100152,Human_Splice_Rec_1100153,Human_Splice_Rec_1100166,Human_Splice_Rec_1100167 Human_miRNA_ID_550689,Human_miRNA_ID_687303,Human_miRNA_ID_889902,Human_miRNA_ID_1066478,Human_miRNA_ID_1077818,Human_miRNA_ID_2195325 RMVar_hsa_circ_78150,RMVar_hsa_circ_260891 117297 RMVar_ID_117297 Human_SNP_ID_879963237 m1A Human chr9 - 100145401 100145401 100145401 TTTGCACCCCAATCCCTTATTTCCATGCCCTGACTTCTTATCTCTGCACCCCATCCCTTATTTCC TTTGCACCCCAATCCCTTATTTCCATGCCCTGTCTTCTTATCTCTGCACCCCATCCCTTATTTCC T A - - Other Unknown GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA Glucose starvation 4h chr9:100145091..100145512 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 117298 RMVar_ID_117298 Human_SNP_ID_879964676 m1A Human chr9 - 95004288 95004288 95004288 TGTTTTCATAATTAGGGAGAAAGTTTACACTTACTTTATAAAAATGTGCGATACCCCAAGATTTT TGTTTTCATAATTAGGGAGAAAGTTTACACTTGCTTTATAAAAATGTGCGATACCCCAAGATTTT T C - - Other Unknown GSE70485:GSM1972531,GSM1972532 HEPG2 cell line,mRNA heat shock 4h chr9:95004237..95004346 26863196 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 117299 RMVar_ID_117299 Human_SNP_ID_879969059 m1A Human chr9 + 93259404 93259404 93259404 CCGGCACTGCCTCCACAACCCACACTGCCCCCACAACCCGTGCTGCCCCCGCAACCCACGCTGCC CCGGCACTGCCTCCACAACCCACACTGCCCCCCCAACCCGTGCTGCCCCCGCAACCCACGCTGCC A C WNK2 Ensembl:ENSG00000165238 Protein coding 5'UTR GSE70485:GSM1782888,GSM1782889,GSM1782890,GSM1782891 HeLa cell line,mRNA chr9:93252934..93261958 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver Human_RBP_ID_5135475,Human_RBP_ID_17094640,Human_RBP_ID_18962102 Human_miRNA_ID_1421805 117300 RMVar_ID_117300 Human_SNP_ID_879971107 m1A Human chr9 + 127937501 127937501 127937501 TGATCAGGCTAACGGCGACGAGGCCGAGTCCCACCACCTGGTCTGTCCCCGTGGCCTGGAGAAAA TGATCAGGCTAACGGCGACGAGGCCGAGTCCCTCCACCTGGTCTGTCCCCGTGGCCTGGAGAAAA A T AL157935.2 Ensembl:ENSG00000227218 lincRNA intron GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525;GSE70485:GSM1972527,GSM1972528,GSM1972529,GSM1972530 HEPG2 cell line,mRNA untreated;HEPG2 cell line,mRNA Glucose starvation 4h chr9:127937396..127937525;chr9:127937426..127937525 26863196 MeRIP-seq:(Medium) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 117301 RMVar_ID_117301 Human_SNP_ID_879982927 m1A Human chr9 + 93452297 93452297 93452297 AGACGGCACAGCAGATCGTCAGCCATGTCCAGAACAAGGGCACCCCGCCGCCAAAGGTCTGGTTC AGACGGCACAGCAGATCGTCAGCCATGTCCAGCACAAGGGCACCCCGCCGCCAAAGGTCTGGTTC A C FAM120A Ensembl:ENSG00000048828 Protein coding CDS GSE135403:GSM4007700,GSM4007701,GSM4007702,GSM4007703 HTR8/Svneo,Normoxia chr9:93452253..93452403 32194978 MeRIP-seq:(Medium) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma,KIRP 5 kidney Human_RBP_ID_16740960,Human_RBP_ID_18453790,Human_RBP_ID_27377036 Human_Splice_Rec_1062637,Human_Splice_Rec_1062671,Human_Splice_Rec_1062687 Human_miRNA_ID_2146562,Human_miRNA_ID_2987987,Human_miRNA_ID_3021685 RMVar_hsa_circ_82156,RMVar_hsa_circ_257860 117302 RMVar_ID_117302 Human_SNP_ID_879985338 m1A Human chr9 - 134040176 134040176 134040176 AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGAAGAAGGACAAGGAGAAGGAGAAGGAGAAGCAC AGAAGAAGGAGAAGAAGGAGAAGGAGAAGAAGGAGAAGGACAAGGAGAAGGAGAAGGAGAAGCAC T C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE70485:GSM1972519,GSM1972520,GSM1972521,GSM1972522,GSM1972523,GSM1972524,GSM1972525 HEPG2 cell line,mRNA untreated chr9:134040026..134041914 26863196 MeRIP-seq:(Medium) rs1564549210 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_219872,Human_RBP_ID_1708046,Human_RBP_ID_5017964,Human_RBP_ID_9407740,Human_RBP_ID_24392489,Human_RBP_ID_24549674,Human_RBP_ID_24563640,Human_RBP_ID_26361383,Human_RBP_ID_27832903 Human_Splice_Rec_1096840,Human_Splice_Rec_1096868 RMVar_hsa_circ_832,RMVar_hsa_circ_260696 117303 RMVar_ID_117303 Human_SNP_ID_879995574 m1A Human chr9 - 37592573 37592573 37592573 CGAGTTCCGGGCGCGAGGCGGCCACCGTGGAGAGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCA CGAGTTCCGGGCGCGAGGCGGCCACCGTGGAGGGCAGAGCGCGGCGGCTGGAAGCTGCTAAGTCA T C AL138752.2,TOMM5 Ensembl:ENSG00000255872,Ensembl:ENSG00000175768 Protein coding,Protein coding intron,5'UTR GSE123365:GSM3896231,GSM3896232,GSM3896233,GSM3896234,GSM3896235,GSM3896236 HEK-293T cells,m1A-IP-seq - 31548705 m1A-IP-seq:(High) rs1289094002 Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck Human_RBP_ID_798435,Human_RBP_ID_5035695,Human_RBP_ID_22466840,Human_RBP_ID_26360374